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SDLRC - Scientific Articles all years by Author - Wh+
The Sheahan Diamond Literature Reference Compilation
The Sheahan Diamond Literature Reference Compilation is compiled by Patricia Sheahan who publishes on a monthly basis a list of new scientific articles related to diamonds as well as media coverage and corporate announcementscalled the Sheahan Diamond Literature Service that is distributed as a free pdf to a list of followers. Pat has kindly agreed to allow her work to be made available as an online digital resource at Kaiser Research Online so that a broader community interested in diamonds and related geology can benefit. The references are for personal use information purposes only; when available a link is provided to an online location where the full article can be accessed or purchased directly. Reproduction of this compilation in part or in whole without permission from the Sheahan Diamond Literature Service is strictly prohibited. Return to Diamond Resource Center
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
The SDLRC provides 3 types of references identified in the reference code. DS for scientific article, DM for a media article, and DC for a corporate announcement. Consider DS0512-0001. The DS stands for "diamond scientific". 05 stands for 2005, the year the reference was posted. 12 represents the month the reference was posted. For all years prior to 2015 the default month is 12. -0001 is the reference's identifier and it does not mean anything. The number below the refence code, ie 2015, is the year the article was published. Note that the posted year may sometimes be later than the published year.
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Abstract: The Cenozoic East African rift (EAR), Cameroon Volcanic Line (CVL), and Atlas Mountains formed on the slow-moving African continent, which last experienced orogeny during the Pan-African. We synthesize primarily geophysical data to evaluate the role of magmatism in shaping Africa's crust. In young magmatic rift zones, melt and volatiles migrate from the asthenosphere to gas-rich magma reservoirs at the Moho, altering crustal composition and reducing strength. Within the southernmost Eastern rift, the crust comprises ~20% new magmatic material ponded in the lower crust and intruded as sills and dikes at shallower depths. In the Main Ethiopian Rift, intrusions comprise 30% of the crust below axial zones of dike-dominated extension. In the incipient rupture zones of the Afar rift, magma intrusions fed from crustal magma chambers beneath segment centers create new columns of mafic crust, as along slow-spreading ridges. Our comparisons suggest that transitional crust, including seaward dipping sequences, is created as progressively smaller screens of continental crust are heated and weakened by magma intrusion into 15-20 km thick crust. In the 30 Ma Recent CVL, which lacks a hot spot age progression, extensional forces are small, inhibiting the creation and rise of magma into the crust. In the Atlas orogen, localized magmatism follows the strike of the Atlas Mountains from the Canary Islands hot spot toward the Alboran Sea. CVL and Atlas magmatism has had minimal impact on crustal structure. Our syntheses show that magma and volatiles are migrating from the asthenosphere through the plates, modifying rheology, and contributing significantly to global carbon and water fluxes.
International Journal of Earth Sciences, in press available, 27p.
Africa, Zimbabwe
Geophysics - magnetics
Abstract: Regional aeromagnetic data from the south-central Zimbabwe Craton have been digitally processed and enhanced for geological and structural mapping and tectonic interpretation integrated with gravity data, to constrain previous interpretations based on tentative geologic maps and provide new information to link these structural features to known tectonic events. The derived maps show excellent correlation between magnetic anomalies and the known geology, and extend lithological and structural mapping to the shallow/near subsurface. In particular, they reveal the presence of discrete crustal domains and several previously unrecognised dykes, faults, and ultramafic intrusions, as well as extensions to others. Five regional structural directions (ENE, NNE, NNW, NW, and WNW) are identified and associated with trends of geological units and cross-cutting structures. The magnetic lineament patterns cut across the >2.7 Ga greenstone belts, which are shown by gravity data to be restricted to the uppermost 10 km of the crust. Therefore, the greenstone belts were an integral part of the lithosphere before much of the upper crustal (brittle) deformation occurred. Significantly, the observed magnetic trends have representatives craton-wide, implying that our interpretation and inferences can be applied to the rest of the craton with confidence. Geological-tectonic correlation suggests that the interpreted regional trends are mainly 2.5 Ga (Great Dyke age) and younger, and relate to tectonic events including the reactivation of the Limpopo Belt at 2.0 Ga and the major regional igneous/dyking events at 1.8-2.0 Ga (Mashonaland), 1.1 Ga (Umkondo), and 180 Ma (Karoo). Thus, their origin is here inferred to be inter- and intra-cratonic collisions and block movements involving the Zimbabwe and Kaapvaal Cratons and the Limpopo Belt, and later lithospheric heating and extension associated with the break-up of Gondwana. The movements produced structures, or reactivated older fractures, that were exploited by Late Archaean and Proterozoic mafic intrusions. There was interplay between vertical and horizontal tectonics as seen in similar terrains worldwide.
International Journal of Earth Sciences, Vol. 105, 8, pp. 2175-2201.
Africa, Zimbabwe
Geophysics - gravity
Abstract: Regional aeromagnetic data from the south-central Zimbabwe Craton have been digitally processed and enhanced for geological and structural mapping and tectonic interpretation integrated with gravity data, to constrain previous interpretations based on tentative geologic maps and provide new information to link these structural features to known tectonic events. The derived maps show excellent correlation between magnetic anomalies and the known geology, and extend lithological and structural mapping to the shallow/near subsurface. In particular, they reveal the presence of discrete crustal domains and several previously unrecognised dykes, faults, and ultramafic intrusions, as well as extensions to others. Five regional structural directions (ENE, NNE, NNW, NW, and WNW) are identified and associated with trends of geological units and cross-cutting structures. The magnetic lineament patterns cut across the >2.7 Ga greenstone belts, which are shown by gravity data to be restricted to the uppermost 10 km of the crust. Therefore, the greenstone belts were an integral part of the lithosphere before much of the upper crustal (brittle) deformation occurred. Significantly, the observed magnetic trends have representatives craton-wide, implying that our interpretation and inferences can be applied to the rest of the craton with confidence. Geological-tectonic correlation suggests that the interpreted regional trends are mainly 2.5 Ga (Great Dyke age) and younger, and relate to tectonic events including the reactivation of the Limpopo Belt at 2.0 Ga and the major regional igneous/dyking events at 1.8-2.0 Ga (Mashonaland), 1.1 Ga (Umkondo), and 180 Ma (Karoo). Thus, their origin is here inferred to be inter- and intra-cratonic collisions and block movements involving the Zimbabwe and Kaapvaal Cratons and the Limpopo Belt, and later lithospheric heating and extension associated with the break-up of Gondwana. The movements produced structures, or reactivated older fractures, that were exploited by Late Archaean and Proterozoic mafic intrusions. There was interplay between vertical and horizontal tectonics as seen in similar terrains worldwide.
International Journal of Earth Sciences, Vol. 105, 8, pp. 2175-2201.
Africa, Zimbabwe
Geophysics - magnetics
Abstract: Regional aeromagnetic data from the south-central Zimbabwe Craton have been digitally processed and enhanced for geological and structural mapping and tectonic interpretation integrated with gravity data, to constrain previous interpretations based on tentative geologic maps and provide new information to link these structural features to known tectonic events. The derived maps show excellent correlation between magnetic anomalies and the known geology, and extend lithological and structural mapping to the shallow/near subsurface. In particular, they reveal the presence of discrete crustal domains and several previously unrecognised dykes, faults, and ultramafic intrusions, as well as extensions to others. Five regional structural directions (ENE, NNE, NNW, NW, and WNW) are identified and associated with trends of geological units and cross-cutting structures. The magnetic lineament patterns cut across the >2.7 Ga greenstone belts, which are shown by gravity data to be restricted to the uppermost 10 km of the crust. Therefore, the greenstone belts were an integral part of the lithosphere before much of the upper crustal (brittle) deformation occurred. Significantly, the observed magnetic trends have representatives craton-wide, implying that our interpretation and inferences can be applied to the rest of the craton with confidence. Geological-tectonic correlation suggests that the interpreted regional trends are mainly 2.5 Ga (Great Dyke age) and younger, and relate to tectonic events including the reactivation of the Limpopo Belt at 2.0 Ga and the major regional igneous/dyking events at 1.8-2.0 Ga (Mashonaland), 1.1 Ga (Umkondo), and 180 Ma (Karoo). Thus, their origin is here inferred to be inter- and intra-cratonic collisions and block movements involving the Zimbabwe and Kaapvaal Cratons and the Limpopo Belt, and later lithospheric heating and extension associated with the break-up of Gondwana. The movements produced structures, or reactivated older fractures, that were exploited by Late Archaean and Proterozoic mafic intrusions. There was interplay between vertical and horizontal tectonics as seen in similar terrains worldwide.
Abstract: Over the last few decades, significant advances in using geophysical techniques to image the structure of magma plumbing systems have enabled the identification of zones of melt accumulation, crystal mush development, and magma migration. Combining advanced geophysical observations with petrological and geochemical data has arguably revolutionised our understanding of, and afforded exciting new insights into, the development of entire magma plumbing systems. However, divisions between the scales and physical settings over which these geophysical, petrological, and geochemical methods are applied still remain. To characterise some of these differences and promote the benefits of further integration between these methodologies, we provide a review of geophysical techniques and discuss how they can be utilised to provide a structural context for and place physical limits on the chemical evolution of magma plumbing systems. For example, we examine how Interferometric Synthetic Aperture Radar (InSAR), coupled with Global Positioning System (GPS) and Global Navigation Satellite System (GNSS) data, and seismicity may be used to track magma migration in near real-time. We also discuss how seismic imaging, gravimetry, and electromagnetic data can identify contemporary melt zones, magma reservoirs, and, or, crystal mushes. These techniques complement seismic reflection data and rock magnetic analyses that delimit the structure and emplacement of ancient magma plumbing systems. For each of these techniques, with the addition of full-waveform inversion (FWI), the use of Unmanned Aerial Vehicles (UAVs), and the integration of geophysics with numerical modelling, we discuss potential future directions. We show that approaching problems concerning magma plumbing systems from an integrated petrological, geochemical, and geophysical perspective will undoubtedly yield important scientific advances, providing exciting future opportunities for the volcanological community.
Contributions to Mineralogy and Petrology, dor.org/10.1007/ s00410-020-01750-9 27p. Pdf
Mantle
Geothermometry
Abstract: The interplay between stress and chemical processes is a fundamental aspect of how rocks evolve, relevant for understanding fracturing due to metamorphic volume change, deformation by pressure solution and diffusion creep, and the effects of stress on mineral reactions in crust and mantle. There is no agreed microscale theory for how stress and chemistry interact, so here I review support from eight different types of the experiment for a relationship between stress and chemistry which is specific to individual interfaces: (chemical potential)?=?(Helmholtz free energy)?+?(normal stress at interface)?×?(molar volume). The experiments encompass temperatures from -100 to 1300 degrees C and pressures from 1 bar to 1.8 GPa. The equation applies to boundaries with fluid and to incoherent solid-solid boundaries. It is broadly in accord with experiments that describe the behaviours of free and stressed crystal faces next to solutions, that document flow laws for pressure solution and diffusion creep, that address polymorphic transformations under stress, and that investigate volume changes in solid-state reactions. The accord is not in all cases quantitative, but the equation is still used to assist the explanation. An implication is that the chemical potential varies depending on the interface, so there is no unique driving force for reaction in stressed systems. Instead, the overall evolution will be determined by combinations of reaction pathways and kinetic factors. The equation described here should be a foundation for grain-scale models, which are a prerequisite for predicting larger scale Earth behaviour when stress and chemical processes interact. It is relevant for all depths in the Earth from the uppermost crust (pressure solution in basin compaction, creep on faults), reactive fluid flow systems (serpentinisation), the deeper crust (orogenic metamorphism), the upper mantle (diffusion creep), the transition zone (phase changes in stressed subducting slabs) to the lower mantle and core mantle boundary (diffusion creep).
Contributions to mineralogy and Petrology, Vol. 175, 27p. Pdf
Mantle
mineralogy, geochemistry
Abstract: The interplay between stress and chemical processes is a fundamental aspect of how rocks evolve, relevant for understanding fracturing due to metamorphic volume change, deformation by pressure solution and diffusion creep, and the effects of stress on mineral reactions in crust and mantle. There is no agreed microscale theory for how stress and chemistry interact, so here I review support from eight different types of the experiment for a relationship between stress and chemistry which is specific to individual interfaces: (chemical potential)?=?(Helmholtz free energy)?+?(normal stress at interface)?×?(molar volume). The experiments encompass temperatures from -100 to 1300 degrees C and pressures from 1 bar to 1.8 GPa. The equation applies to boundaries with fluid and to incoherent solid-solid boundaries. It is broadly in accord with experiments that describe the behaviours of free and stressed crystal faces next to solutions, that document flow laws for pressure solution and diffusion creep, that address polymorphic transformations under stress, and that investigate volume changes in solid-state reactions. The accord is not in all cases quantitative, but the equation is still used to assist the explanation. An implication is that the chemical potential varies depending on the interface, so there is no unique driving force for reaction in stressed systems. Instead, the overall evolution will be determined by combinations of reaction pathways and kinetic factors. The equation described here should be a foundation for grain-scale models, which are a prerequisite for predicting larger scale Earth behaviour when stress and chemical processes interact. It is relevant for all depths in the Earth from the uppermost crust (pressure solution in basin compaction, creep on faults), reactive fluid flow systems (serpentinisation), the deeper crust (orogenic metamorphism), the upper mantle (diffusion creep), the transition zone (phase changes in stressed subducting slabs) to the lower mantle and core mantle boundary (diffusion creep).
Abstract: The bulk of the Earth’s volume is composed of the mantle-the layer of silicate rocks sandwiched between the dense, hot core and the thin crust. Although the mantle is mostly solid rock, it’s generally viscous: Slowly over millions of years, the material within the layer drifts, driving tectonic plates together and apart. Thus, the mantle’s influence can be seen on the planet’s surface on both large and small scales-from fueling volcanoes and seafloor expansion down to the composition and characteristics of igneous rocks. Most of the Earth’s mantle is composed of peridotite, an igneous rock rich in the mineral olivine. But previous research suggests that melted mantle pyroxenites-igneous rocks composed primarily of pyroxenes, minerals that contain 40% more silicon than olivine-may also be a source of oceanic lavas. New research by Lambart et al. seeks to better model how pyroxenites influence melting that occurs in the mantle. Pyroxenites make up between 2% and 10% of the upper mantle, depending on the region, but determining the amount of pyroxenites in hot mantle plumes to the surface requires more information. Researchers have found that at the same pressure, pyroxenites tend to melt at lower temperatures than peridotites, which means that any pyroxenites in peridotite-rich mantle regions might make up a larger portion of the liquid material than their small fraction of mantle bulk would suggest. To understand how the varying source materials in the mantle contribute to the characteristics of igneous rocks at the surface, researchers need to understand the melting characteristics of pyroxenites-a broad and variable group of rocks. That variability in composition makes predicting the phase changes of pyroxenites more complicated. And that complexity means that current models of mantle melting, like pMELTS, overestimate the temperature range over which pyroxenites melt. So the authors created a new parameterization for mantle melting models that seeks to rectify the problem. The new parameterization accounts for the fact that temperature, pressure, and the bulk chemical composition of the rocks together determine their near solidus temperature. The authors used a compilation of 183 experiments on pyroxenites with 25 varying chemical compositions, carried out over pressures from 0.9 to 5 gigapascals (GPa) and temperatures ranging from 1150°C to 1675°C. They charted the temperature when 5% of the materials was molten and the temperature at which clinopyroxene, a dominant mineral in pyroxenites, in each sample was gone-parameters that are easy to detect accurately and consistently. This analysis helped the authors create a new model based on experimental data from the literature, dubbed Melt-PX, which predicts the temperature at which the pyroxenites start to melt within 30°C and the amount of melting within 13%. It showed that at low pressure-less than 1 GPa-pyroxenites melt at lower temperatures than peridotites, but as pressure increases, more and more pyroxenites melt at higher temperatures than peridotites. The new model will be a useful tool to understand magma composition, ultimately giving researchers a window into the Earth and the source of oceanic basalts.
Tsuji, L.J.S., McCarthy, D.D., Whielaw, G.S., McEachren, J.
Getting back to basics: the Victor diamond mine environmental assessment scoping process and the issue of family based traditional lands versus traplines.
Impact Assessment and Project Aapraisal, Vol. 29, 1, pp. 37-47.
43rd Annual Yellowknife Geoscience Forum Abstracts, abstract p. 109.
Canada, Northwest Territories
Deposit - Kennady North
Abstract: The Kennady North Property, wholly owned by Kennady Diamonds Inc. (KDI) is located 300 km northeast of Yellowknife adjacent to the DeBeers/Mountain Province Gahcho Kué mine site. Exploration on the property dates back to the early 90’s, during which time several kimberlites were discovered. Since 2012 Kennady Diamonds has completed a number of geophysical, hand and RC till sampling and diamond drill programs. In 2015, KDI completed a large diameter reverse circulation drill program to bulk sample the southern lobe of the Kelvin kimberlite. Following the RC program, diamond drilling and ground geophysical surveys continued in the Kelvin-Faraday Corridor (KFC) and at various exploration targets on the property including the MZ Dyke and Doyle Sill. The field season started in January with the completion of the Kelvin camp and the construction of the RC drill icepad on Kelvin Lake. The pad and a seasonal spur road off the Gahcho Kue seasonal road were completed to coincide with the opening of the Tibbit-Contwoyto winter road and facilitated the mobilization of two large diameter RC rigs operated by Midnight Sun Drilling Inc. to the property. A total of 446 tonnes of the Kelvin kimberlite were obtained via RC drilling between February 19 and April 2. The bulk sample was processed via DMS at the Saskatchewan Research Council in Saskatoon. One diamond drill commenced drilling prior to the RC program and two other drills commenced on the heels of the RC program. A total of 31,000 meters of NQ and HQ core have been drilled during 2015 to the end of October. Drilling at Kelvin has focused on geotechnical and related environmental baseline work as well as further delineation of the pipe-like body with the aim of generating a NI43-101 compliant resource in early 2016. Diamond drilling at the Faraday group of kimberlites delineated the Faraday 1 and Faraday 2 kimberlites. These pipe-like bodies share a similar pipe-like structure and internal geology to the Kelvin kimberlite. Aurora conducted 8848 stations of ground gravity and 521.32 line-kilometers of OhmmapperTM capacitively coupled resistivity in the KFC, MZ dyke, and Doyle Sill during March and April. A 87 line-kilometer bubble seismic survey over the Kelvin, Faraday and MZ complexes was conducted in September. Kennady Diamond Inc. is very encouraged by the exploration results to date and anticipates a successful and exciting 2016.
Re-thinking diamond exploration tactics in the Slave Province: a surficial geology perspective. Lac de Gras area
2018 Yellowknife Geoscience Forum , p. 66-67. abstract
Canada, Northwest Territories
geochemistry
Abstract: It took several decades to develop the necessary understanding of glaciation, geochemistry and mineralogy to refine exploration strategies and find the first kimberlite in the Northwest Territories, Canada. These fundamental drift prospecting strategies followed by geophysics and drilling have been used to locate many kimberlite occurrences over the years. Indicator minerals in surface sediments are still the primary datasets used to identify kimberlite exploration targets; however, many of the kimberlite sources for the well-defined indicator mineral dispersals have been identified. Exploration must now focus on regions with more complex surficial geology where primary dispersal patterns in till are obscured by post-depositional modification. These patterns are largely defined using data from historical “˜till' surveys that often failed to properly scrutinize the sample media; reworked tills and other surficial materials were commonly collected. The regional surficial geology maps (e.g., 1:50,000 to 1:250,000) typically published by geological surveys to stimulate reconnaissance exploration in new areas are generally incapable of providing sufficient resolution to determine the genesis and post-glacial alteration of sample media or reconcile complex dispersal patterns. Furthermore, advances in analytical methods have yielded compiled datasets with results from multiple methods that are not always comparable. Without a new, more detailed and systematic approach to evaluating surface sediment data, exploration in areas with complex glacial, deglacial and post-glacial histories will be challenged to discover kimberlite. The accessibility, quality and variety of high-resolution aerial or satellite imagery and topographic data has improved significantly over the years, affording a more detailed interpretation of the surficial environment. These detailed interpretations have allowed us to evaluate historical data with a new perspective and target the collection of new, high-quality data. Throughout the Slave Province, we have tailored surficial interpretations to distinguish in-situ till from reworked till and other materials, which have altered dispersion and indicator mineral concentrations. Using examples from the Lac de Gras area, this presentation demonstrates how a detailed surficial framework, combined with an understanding of the varied analytical methods, is applied to historical datasets to refine indicator dispersal patterns and identify new exploration targets. By standardizing the data based on sediment genesis and transport mechanisms, the dataset becomes more suitable for statistical evaluation and anomaly threshold determinations that are unique to specific data subpopulations. As a result, anomaly contrasts are improved, and complex dispersals can be unravelled. In addition, areas with insufficient data coverage are identified and the necessary framework to complete informed, efficient infill or new sampling is provided. The examples we share highlight that there is no replacement for project-scale understanding of surficial geology and its varied effects on mineral dispersals in the development and interpretation of a surface sediment dataset used to identify kimberlite exploration targets.
43rd Annual Yellowknife Geoscience Forum Abstracts, abstract p. 24.
Canada, Northwest Territories
Deposit - Ekati
Abstract: How would a large open pit mine on caribou range (e.g., the Ekati Diamond Mine in the Bathurst caribou’s summer range) have influenced caribou? A traditional knowledge study on the cumulative impacts on the Bathurst caribou herd qualitatively described how mining activities might have influenced the herd (Mackenzie et al. 2013): caribou migration routes deflected away from the mines probably due to seeing mining activities or hearing the noises; and skinny caribou or abnormal smells and materials in caribou meat, liver, or the hide linings probably related to changes in caribou forage and quality of water and air. In other words, the potential influences of mining operations on caribou were most likely through altering what caribou can see, hear, smell (e.g., dusts and fine particle matter < 2.5 ?m (PM2.5) in the air, and from acidity in the soil), and taste (e.g., dust on foliage, vegetation composition change). Boulanger et al. (2012) estimated the size of a zone of influence (ZOI) of the Ekati-Diavik mining complex in the Bathurst caribou summer range, using caribou presence dataset. They also explored the mechanisms of ZOI using the spatial distribution of the total suspended particles, which was simulated with an atmospheric transport and dispersion model (Rescan, 2006). While these studies have added to our understanding of the possible impacts of mining operations on caribou, knowledge gaps remain. One outstanding gap is the lack of direct measurements about the caribou relevant environmental changes caused by mining operations. For example, exactly from how far away can caribou clearly see the vehicles driving on a mining road, or the buildings and the elevated waste piles in a camp? From how far away might caribou hear the noise caused by mining operations? To what spatial extent had the dusts and PM2.5 from mining operations influenced the tundra ecosystems? And how the dusts and PM2.5 from mining operations might have influenced caribou forage quality? Potentially these questions can be answered by in-situ measurements and satellite remote sensing. For example, studies have showed that it is possible to remotely sense PM2.5 distribution using twice-daily MODIS data at a spatial resolution of 1 km (Lyapustin et al., 2011; Chudnovsky et al., 2013; Hu et al., 2014). The objective of this study is thus to quantitatively measure these changes around the Ekati Diamond Mine, by means of in-situ surveys and satellite remote sensing. We conducted field surveys at more than 100 sites around the Ekati Diamond Mine during August 14-23, 2015, a collaborative effort of the NWT CIMP project entitled “Satellite Monitoring for Assessing Resource Development’s Impact on Bathurst Caribou (SMART)”, and the Dominion Diamond Ekati Corporation. In this presentation, we will report preliminary results and lessons learned from our first year’s study.
Deep crustal deformation textures along megathrusts from Newfoundland andOntario: implications for microstructural preservation, strain rates and strength of the li
Canadian Journal of Earth Sciences, Vol. 29, No. 2, Feb. pp. 328-337
Ross, P., White, J.D., Lorenz, V., Zimanowski, B., Boettner, R., McClintock, M.
Why lower diatremes in kimberlitic and non-kimberlitic systems are non-stratified, homogenized, and contain steep internal contacts: episodic burst and debris jets.
GAC/MAC/AGU Meeting held May 23-27 Toronto, Abstract only
Quantification of vesicle characteristerics in some diatreme filling deposits, and the explosivity levels of magma water interactions within diatremes.
Journal of Geothermal Volcanology and Research, Vol. 245-246, pp. 55-67.
Valentine, G.A., Graettinger, A.H, Macorps, E., Ross, P-S., White, J.D.L., Dohring, E., Sonder, I.
Experiments with vertically and laterally migrating subsurface explosions with applications to the geology of phreatomagmatic and hydrothermal explosion craters and diatremes.
Abstract: Gem-quality diamonds have been found in several alluvial deposits across central and southern Borneo. Borneo has been a known source of diamonds for centuries, but the location of their primary igneous source remains enigmatic. Many geological models have been proposed to explain their distribution, including: the diamonds were derived from a local diatreme; they were brought to the surface through ophiolite obduction or exhumation of UHP metamorphic rocks; they were transported long distances southward via major Asian river systems; or, they were transported from the Australian continent before Borneo was rifted from its northwestern margin in the Late Jurassic. To assess these models, we conducted a study of the provenance of heavy minerals from Kalimantan's Cempaka alluvial diamond deposit. This involved collecting U Pb isotopic data, fission track and trace element geochemistry of zircon as well as major element geochemical data of spinels and morphological descriptions of zircon and diamond. The results indicate that the Cempaka diamonds were likely derived from at least two sources, one which was relatively local and/or involved little reworking, and the other more distal which records several periods of reworking. The distal diamond source is interpreted to be diamond-bearing pipes that intruded the basement of a block that: (1) rifted from northwest Australia (East Java or SW Borneo) and the diamonds were recycled into its sedimentary cover, or: (2) were emplaced elsewhere (e.g. NW Australia) and transported to a block (e.g. East Java or SW Borneo). Both of these scenarios require the diamonds to be transported with the block when it rifted from NW Australia in the Late Jurassic. The local source could be diamondiferous diatremes associated with eroded Miocene high-K alkaline intrusions north of the Barito Basin, which would indicate that the lithosphere beneath SW Borneo is thick (~ 150 km or greater). The ‘local’ diamonds could also be associated with ophiolitic rocks that are exposed in the nearby Meratus Mountains.
Angewandte Chemie International, Vol. 60, 3, pp. 1546-1549. pdf
Global
diamond, graphite
Abstract: Recent density?functional theory (DFT) calculations raised the possibility that diamond could be degenerate with graphite at very low temperatures. Through high?accuracy calorimetric experiments closing gaps in available data, we reinvestigate the relative thermodynamic stability of diamond and graphite. For T<400 K, graphite is always more stable than diamond at ambient pressure. At low temperatures, the stability is enthalpically driven, and entropy terms add to the stability at higher temperatures. We also carried out DFT calculations: B86bPBE?25X?XDM//B86bPBE?XDM and PBE0?XDM//PBE?XDM results overlap with the experimental ?T?S results and bracket the experimental values of ?H and ?G, displaced by only about 2× the experimental uncertainty. Revised values of the standard thermodynamic functions for diamond are ?fHo=?2150±150 J?mol?1, ?fSo=3.44±0.03 J?K?1?mol?1 and ?fGo=?3170±150 J?mol?1.
Abstract: Convective circulation of the Earth’s mantle maintains some fraction of surface topography that varies with space and time. Most predictive models show that this dynamic topography has peak amplitudes of about ±2?km, dominated by wavelengths of 104?km. Here, we test these models against our comprehensive observational database of 2,120 spot measurements of dynamic topography that were determined by analysing oceanic seismic surveys. These accurate measurements have typical peak amplitudes of ±1?km and wavelengths of approximately 103?km, and are combined with limited continental constraints to generate a global spherical harmonic model, the robustness of which has been carefully tested and benchmarked. Our power spectral analysis reveals significant discrepancies between observed and predicted dynamic topography. At longer wavelengths (such as 104?km), observed dynamic topography has peak amplitudes of about ±500?m. At shorter wavelengths (such as 103?km), significant dynamic topography is still observed. We show that these discrepancies can be explained if short-wavelength dynamic topography is generated by temperature-driven density anomalies within a sub-plate asthenospheric channel. Stratigraphic observations from adjacent continental margins show that these dynamic topographic signals evolve quickly with time. More rapid temporal and spatial changes in vertical displacement of the Earth’s surface have direct consequences for fields as diverse as mantle flow, oceanic circulation and long-term climate change.
Abstract: Tectonic plate interiors are often regarded as relatively inactive. Yet, reconstructions of marine terrace uplift in Angola suggest that underlying mantle flow can rapidly warp Earth's surface far from obviously active plate boundaries.
Earth and Planetary Science Letters, Vol. 496, 1, pp. 142-158.
Asia, Borneo
convection
Abstract: Most, but not all, geodynamic models predict 1-2 km of mantle convective draw-down of the Earth's surface in a region centered on Borneo within southeast Asia. Nevertheless, there is geomorphic, geologic and geophysical evidence which suggests that convective uplift might have played some role in sculpting Bornean physiography. For example, a long wavelength free-air gravity anomaly of +60 mGal centered on Borneo coincides with the distribution of Neogene basaltic magmatism and with the locus of sub-plate slow shear wave velocity anomalies. Global positioning system measurements, an estimate of elastic thickness, and crustal isostatic considerations suggest that regional shortening does not entirely account for kilometer-scale regional elevation. Here, we explore the possible evolution of the Bornean landscape by extracting and modeling an inventory of 90 longitudinal river profiles. Misfit between observed and calculated river profiles is minimized by smoothly varying uplift rate as a function of space and time. Erosional parameters are chosen by assuming that regional uplift post-dates Eocene deposition of marine carbonate rocks. The robustness of this calibration is tested against independent geologic observations such as thermochronometric measurements, offshore sedimentary flux calculations, and the history of volcanism. A calculated cumulative uplift history suggests that kilometer-scale Bornean topography grew rapidly during Neogene times. This suggestion is corroborated by an offshore Miocene transition from carbonate to clastic deposition. Co-location of regional uplift and slow shear wave velocity anomalies immediately beneath the lithospheric plate implies that regional uplift could have been at least partly generated and maintained by temperature anomalies within an asthenospheric channel.
Earth and Planetary Science Letters, Vol. 542, 116317 16p. Pdf
Mantle
plumes, geothermometry
Abstract: Mantle convection is the principal mechanism by which heat is transferred from the deep Earth to the surface. Cold subducting slabs sink into the mantle and steadily warm, whilst upwelling plumes carry heat to the base of lithospheric plates where it can subsequently escape by conduction. Accurate estimation of the total heat carried by these plumes is important for understanding geodynamic processes and Earth's thermal budget. Existing estimates, based upon swell geometries and velocities of overriding plates, yield a global heat flux of ?2 TW and indicate that plumes play only a minor role in heat transfer. Here, we revisit the Icelandic and Hawaiian plumes to show that their individual flux estimates are likely to be incorrect due to the assumption that buoyancy is mainly produced within the lithosphere and therefore translates at plate velocities. We develop an alternative methodology that depends upon swell volume, is independent of plate velocities, and allows both for decay of buoyancy through time and for differential motion between asthenospheric buoyancy and the overlying plate. Reanalysis of the Icelandic and Hawaiian swells yields buoyancy fluxes of Mg s?1 and Mg s?1, respectively. Both swells are used to calibrate a buoyancy decay timescale of ?45 Myr for the new volumetric approach, which enables buoyancy fluxes to be estimated for a global inventory of 53 swells. Estimates from magmatic hotspots yield a cumulative lower bound on global plume flux of 2 TW, which increases to 6 TW if amagmatic swells are also included and if all buoyancy is assumed to be thermal in origin. Our results suggest that upwelling plumes play a significant role in the transfer of heat into the uppermost mantle.
Earth and Planetary Science Letters, Vol. 432, pp. 159-168.
Europe, Iceland
Mantle plume
Abstract: The presence of a mantle plume beneath Iceland has long been hypothesised to explain its high volumes of crustal volcanism. Practical constraints in seismic tomography mean that thin, slow velocity anomalies representative of a mantle plume signature are difficult to image. However it is possible to infer the presence of temperature anomalies at depth from the effect they have on phase transitions in surrounding mantle material. Phase changes in the olivine component of mantle rocks are thought to be responsible for global mantle seismic discontinuities at 410 and 660 km depth, though exact depths are dependent on surrounding temperature conditions. This study uses P to S seismic wave conversions at mantle discontinuities to investigate variation in topography allowing inference of temperature anomalies within the transition zone. We employ a large data set from a wide range of seismic stations across the North Atlantic region and a dense network in Iceland, including over 100 stations run by the University of Cambridge. Data are used to create over 6000 receiver functions. These are converted from time to depth including 3D corrections for variations in crustal thickness and upper mantle velocity heterogeneities, and then stacked based on common conversion points. We find that both the 410 and 660 km discontinuities are depressed under Iceland compared to normal depths in the surrounding region. The depression of 30 km observed on the 410 km discontinuity could be artificially deepened by un-modelled slow anomalies in the correcting velocity model. Adding a slow velocity conduit of ?1.44% reduces the depression to 18 km; in this scenario both the velocity reduction and discontinuity topography reflect a temperature anomaly of 210 K. We find that much larger velocity reductions would be required to remove all depression on the 660 km discontinuity, and therefore correlated discontinuity depressions appear to be a robust feature of the data. While it is not possible to definitively rule out the possibility of uncorrected velocity anomalies causing the observed correlated topography we show that this is unlikely. Instead our preferred interpretation is that the 660 km discontinuity is controlled by a garnet phase transition described by a positive Clapeyron slope, such that depression of the 660 is representative of a hot anomaly at depth.
Earth and Planetary Science Letters, Vol. 433, pp. 159-168.
Europe, Iceland
Mantle - 660 km
Abstract: The presence of a mantle plume beneath Iceland has long been hypothesised to explain its high volumes of crustal volcanism. Practical constraints in seismic tomography mean that thin, slow velocity anomalies representative of a mantle plume signature are difficult to image. However it is possible to infer the presence of temperature anomalies at depth from the effect they have on phase transitions in surrounding mantle material. Phase changes in the olivine component of mantle rocks are thought to be responsible for global mantle seismic discontinuities at 410 and 660 km depth, though exact depths are dependent on surrounding temperature conditions. This study uses P to S seismic wave conversions at mantle discontinuities to investigate variation in topography allowing inference of temperature anomalies within the transition zone. We employ a large data set from a wide range of seismic stations across the North Atlantic region and a dense network in Iceland, including over 100 stations run by the University of Cambridge. Data are used to create over 6000 receiver functions. These are converted from time to depth including 3D corrections for variations in crustal thickness and upper mantle velocity heterogeneities, and then stacked based on common conversion points. We find that both the 410 and 660 km discontinuities are depressed under Iceland compared to normal depths in the surrounding region. The depression of 30 km observed on the 410 km discontinuity could be artificially deepened by un-modelled slow anomalies in the correcting velocity model. Adding a slow velocity conduit of ?1.44% reduces the depression to 18 km; in this scenario both the velocity reduction and discontinuity topography reflect a temperature anomaly of 210 K. We find that much larger velocity reductions would be required to remove all depression on the 660 km discontinuity, and therefore correlated discontinuity depressions appear to be a robust feature of the data. While it is not possible to definitively rule out the possibility of uncorrected velocity anomalies causing the observed correlated topography we show that this is unlikely. Instead our preferred interpretation is that the 660 km discontinuity is controlled by a garnet phase transition described by a positive Clapeyron slope, such that depression of the 660 is representative of a hot anomaly at depth.
Abstract: The mechanisms that result in the formation of high-pressure (HP) and ultrahigh-pressure (UHP) rocks are controversial. The usual interpretation assumes that pressure is close to lithostatic, petrological pressure estimates can be transferred to depth, and (U)HP rocks have been exhumed from great depth. An alternative explanation is that pressure can be larger than lithostatic, particularly in continental collision zones, and (U)HP rocks could thus have formed at shallower depths. To better understand the mechanical feasibility of these hypotheses, we performed thermomechanical numerical simulations of a typical subduction and collision scenario. If the subducting crust is laterally homogeneous and has small effective friction angles (and is thus weak), we reproduce earlier findings that <20% deviation of lithostatic pressure occurs within a subduction channel. However, many orogenies involve rocks that are dry and strong, and the crust is mechanically heterogeneous. If these factors are taken into account, simulations show that pressures can be significantly larger than lithostatic within nappe-size, mechanically strong crustal units, or within a strong lower crust, as a result of tectonic deformation. Systematic simulations show that these effects are most pronounced at the base of the crust (at ?40 km), where pressures can reach 2-3 GPa (therefore within the coesite stability field) for millions of years. These pressures are often released rapidly during ongoing deformation. Relating metamorphic pressure estimates to depth might thus be problematic in mechanically heterogeneous crustal rock units that appear to have been exhumed in an ultrafast manner.
Abstract: Self-consistent geodynamic modeling that includes melting is challenging as the chemistry of the source rocks continuously changes as a result of melt extraction. Here, we describe a new method to study the interaction between physical and chemical processes in an uprising heterogeneous mantle plume by combining a geodynamic code with a thermodynamic modeling approach for magma generation and evolution. We pre-computed hundreds of phase diagrams, each of them for a different chemical system. After melt is extracted, the phase diagram with the closest bulk rock chemistry to the depleted source rock is updated locally. The petrological evolution of rocks is tracked via evolving chemical compositions of source rocks and extracted melts using twelve oxide compositional parameters. As a result, a wide variety of newly generated magmatic rocks can in principle be produced from mantle rocks with different degrees of depletion. The results show that a variable geothermal gradient, the amount of extracted melt and plume excess temperature affect the magma production and chemistry by influencing decompression melting and the depletion of rocks. Decompression melting is facilitated by a shallower lithosphere-asthenosphere boundary and an increase in the amount of extracted magma is induced by a lower critical melt fraction for melt extraction and/or higher plume temperatures. Increasing critical melt fractions activates the extraction of melts triggered by decompression at a later stage and slows down the depletion process from the metasomatized mantle. Melt compositional trends are used to determine melting related processes by focusing on K2O/Na2O ratio as indicator for the rock type that has been molten. Thus, a step-like-profile in K2O/Na2O might be explained by a transition between melting metasomatized and pyrolitic mantle components reproducible through numerical modeling of a heterogeneous asthenospheric mantle source. A potential application of the developed method is shown for the West Eifel volcanic field.
Geochemistry, Geophysics, Geosystems, Vol. 20, 4, pp. 1679-1697.
Mantle
plate tectonics
Abstract: It has been believed that early Earth featured higher mantle temperature. The mantle temperature affects the geodynamic processes, and, therefore, the production of the continental crust, which has been a stable environment for the developing of life since Earth's infancy. However, our knowledge of the processes operating during the early Earth is still not definitive. The wide range of the mantle temperature estimation (from 1500 to 1600 °C) hampered our ability to understand early Earth's dynamic and geological data alone cannot provide a definitive answer. Therefore, it is necessary to integrate them with numerical modeling. Our contribution conjugates petrological modeling with thermal?mechanical simulations to unveil the effect of continental crust production. Continental crust's extraction from partially melted hydrated basalts leaves behind dense rocks that sink into the mantle dragging part of surface hydrated rocks. These drips produce a major compositional change of the mantle and promote the production of new basaltic/continental crust. The combination of these processes cools the mantle, suggesting that it could not have been extremely hot for geological timescales. We show that such processes can be active even in a relatively cool mantle (1450-1500 °C), providing new constraints to understand the infancy of our planet.
Journal of Metamorphic Geology, doi.org.10.1111/ jmg.12484
Global
geochemistry
Abstract: This essay in honour of Mike Brown addresses aspects of chemical equilibrium and equilibration in rocks, with a focus on the role that chemical potentials play. Chemical equilibrium is achieved by diffusive flattening of chemical potential gradients. The idea of equilibration volume is developed, and the way equilibration volumes may evolve along a pressure-temperature path is discussed. The effect of the environment of an equilibration volume is key to understanding the evolution of the equilibration volume with changing conditions. The likely behaviour of equilibration volumes is used to suggest why preservation of equilibrium mineral assemblages and mineral compositions from metamorphism tends to occur. This line of logic then provides the conceptual support to conventional equilibrium thermodynamic approaches to studying rocks, using, for example, thermobarometry and pseudosections.
Abstract: Many Archean terranes are interpreted to have a tectonic and metamorphic evolution that indicates intra-crustal reorganization driven by lithospheric-scale gravitational instabilities. These processes are associated with the production of a significant amount of felsic and mafic crust, and are widely regarded to be a consequence of plume-lithosphere interactions. The juvenile Archean felsic crust is made predominantly of rocks of the tonalite-trondhjemite-granodiorite (TTG) suite, which are the result of partial melting of hydrous metabasalts. The geodynamic processes that have assisted the production of juvenile felsic crust, are still not well understood. Here, we perform 2D and 3D numerical simulations coupled with the state-of-the-art of petrological thermodynamical modelling to study the tectonic evolution of a primitive Archean oceanic plateau with particular regard on the condition of extraction of felsic melts. In our numerical simulations, the continuous emplacement of new, dry mafic intrusions and the extraction of the felsic melts, generate an unstable lower crust which drips into the mantle soon after the plume arrival. The subsequent tectonic evolution depends on the asthenosphere TP. If the TP is high enough (? 1500 ?C) the entire oceanic crust is recycled within 2 Myrs. By contrast at low TP, the thin oceanic plateau slowly propagates generating plate-boundary like features.
White-Gaynor, A.L., Nyblade, A.A., Durrheim, R., Raveloson, R., van der Meijde, M., Fadel, I., Paulssen, H., Kwadiba, M., Ntibinyane, O., Titus, N., Sitali, M.
Geochemistry, Geophysics, Geosystems, 10.1029/GC008925 20p. Pdf
Africa, South Africa
Geophysics, seismic
Abstract: We report new P and S wave velocity models of the upper mantle beneath southern Africa using data recorded on seismic stations spanning the entire subcontinent. Beneath most of the Damara Belt, including the Okavango Rift, our models show lower than average velocities (?0.8% Vp; ?1.2% Vs) with an abrupt increase in velocities along the terrane's southern margin. We attribute the lower than average velocities to thinner lithosphere (~130 km thick) compared to thicker lithosphere (~200 km thick) immediately to the south under the Kalahari Craton. Beneath the Etendeka Flood Basalt Province, higher than average velocities (0.25% Vp; 0.75% Vs) indicate thicker and/or compositionally distinct lithosphere compared to other parts of the Damara Belt. In the Rehoboth Province, higher than average velocities (0.3% Vp; 0.5% Vs) suggest the presence of a microcraton, as do higher than average velocities (1.0% Vp; 1.5% Vs) under the Southern Irumide Belt. Lower than average velocities (?0.4% Vp; ?0.7% Vs) beneath the Bushveld Complex and parts of the Mgondi and Okwa terranes are consistent with previous studies, which attributed them to compositionally modified lithosphere resulting from Precambrian magmatic events. There is little evidence for thermally modified upper mantle beneath any of these terranes which could provide a source of uplift for the Southern African Plateau. In contrast, beneath parts of the Irumide Belt in southern and central Zambia and the Mozambique Belt in central Mozambique, deep?seated low velocity anomalies (?0.7% Vp; ?0.8% Vs) can be attributed to upper mantle extensions of the African superplume structure.
Earth and Planetary Science Letters, Vol. 435, 1, pp. 55-63.
Mantle
Plume
Abstract: In order to link the geochemical signature of hot spot basalts to Earth's deep interior, it is first necessary to understand how plumes sample different regions of the mantle. Here, we investigate the relative amounts of deep and shallow mantle material that are entrained by an ascending plume and constrain its source region. The plumes are generated in a viscous syrup using an isolated heater for a range of Rayleigh numbers. The velocity fields are measured using stereoscopic Particle-Image Velocimetry, and the concept of the ‘vortex ring bubble’ is used to provide an objective definition of the plume geometry. Using this plume geometry, the plume composition can be analysed in terms of the proportion of material that has been entrained from different depths. We show that the plume composition can be well described using a simple empirical relationship, which depends only on a single parameter, the sampling coefficient, scsc. High-scsc plumes are composed of material which originated from very deep in the fluid domain, while low-scsc plumes contain material entrained from a range of depths. The analysis is also used to show that the geometry of the plume can be described using a similarity solution, in agreement with previous studies. Finally, numerical simulations are used to vary both the Rayleigh number and viscosity contrast independently. The simulations allow us to predict the value of the sampling coefficient for mantle plumes; we find that as a plume reaches the lithosphere, 90% of its composition has been derived from the lowermost 260–750 km in the mantle, and negligible amounts are derived from the shallow half of the lower mantle. This result implies that isotope geochemistry cannot provide direct information about this unsampled region, and that the various known geochemical reservoirs must lie in the deepest few hundred kilometres of the mantle.
Viljoen, K.S., Harris, J.W., Ivanic, T., Richardson, S.H., Whitehead, K.
Trace element geochemistry and Ni thermometry of garnet inclusions in peridotitic diamonds from Premier and Finsch, South Africa: implications - diamond formation
International Mineralogical Association meeting August Budapest, abstract p. 187.
Abstract: Diamonds from the Machado River alluvial deposit have been characterised on the basis of external morphology, internal textures, carbon isotopic composition, nitrogen concentration and aggregation state and mineral inclusion chemistry. Variations in morphology and features of abrasion suggest some diamonds have been derived directly from local kimberlites, whereas others have been through extensive sedimentary recycling. On the basis of mineral inclusion compositions, both lithospheric and sublithospheric diamonds are present at the deposit. The lithospheric diamonds have clear layer-by-layer octahedral and/or cuboid internal growth zonation, contain measurable nitrogen and indicate a heterogeneous lithospheric mantle beneath the region. The sublithospheric diamonds show a lack of regular sharp zonation, do not contain detectable nitrogen, are isotopically heavy (?13CPDB predominantly ? 0.7 to ? 5.5) and contain inclusions of ferropericlase, former bridgmanite, majoritic garnet and former CaSiO3-perovskite. This suggests source lithologies that are Mg- and Ca-rich, probably including carbonates and serpentinites, subducted to lower mantle depths. The studied suite of sublithospheric diamonds has many similarities to the alluvial diamonds from Kankan, Guinea, but has more extreme variations in mineral inclusion chemistry. Of all superdeep diamond suites yet discovered, Machado River represents an end-member in terms of either the compositional range of materials being subducted to Transition Zone and lower mantle or the process by which materials are transferred from the subducted slab to the diamond-forming region.
Formation and transformation of zircon grains from the Archean carbonatite Siilinjarvi - evidence from cathodluminescence, rare earth elements and U/Pb geochr
Peralk-Carb 2011, workshop held Tubingen Germany June 16-18, Poster
Formation and transformation of zircon grains from the Archean carbonatite Siilinjarvi ( Finland) - evidence from cathodluminescence, rare earth elements and U/Tb
Peralk-Carb 2011... workshop June 16-18, Tubingen, Germany, Abstract p.151-152.
Formation and transformation of zircon grains from the Archean carbonatite Siilinjarvi ( Finland) - evidence from cathodluminescence, rare earth elements and U/Tb
Peralk-Carb 2011... workshop June 16-18, Tubingen, Germany, Abstract p.151-152.
Tichomirowa, M., Whitehouse, M., Gerdes, A., Gotze, J.
Carbonatite metasomatism: evidence from geochemistry and isotope composition ( U-Pb, Hf, O) on zircons from two Precambrian carbonatites of the Kola alkaline province.
Konzett, J., Wirth, R., Hauzenberger, C., Whitehouse, M.
Two episodes of fluid migration in the Kaapvaal Craton lithospheric mantle associated with Cretaceous kimberlite activity: evidence from a harzburgite containing a unique assemblage of metasomatic zirconium-phases.
Abstract: Exhumed ultrahigh-pressure (UHP) terranes, involving slices of deeply subducted crustal rocks, provide unique material for studying material transfer in subduction zones. Diamond-bearing UHP rocks with sedimentary protoliths allow for tracing melting processes at both UHP and UHT including carbon cycling in the Earth. We studied microdiamonds and associated phases in two contrasting lithologies, (1) acid, quartzofeldpathic UHP gneiss composed of garnet, kyanite, feldspar, quartz and biotite, with a high ASI characteristic of sedimentary rocks, and (2) intermediate garnet-clinopyroxene rock containing quartz, feldspar, minor kyanite and biotite, which is metaluminous. Whereas rock (1) contains exclusively single octahedral diamonds with perfect crystal shape in garnet, kyanite (more common) and zircon, the microdiamonds in the rock (2) occur mostly as clusters of cuboid shape in garnet and zircon. Micro-Raman and FIB TEM data document presence of graphite, quartz and rutile at diamond/host interface or in separate multiple solid inclusions (MSI) whereas carbonates are practically absent. The morphology and lack of inclusions reflect relatively slow growth of the octahedral diamonds (rock 1) at lower fluid supersaturation. Individual deep and symmetrical negative trigons (AFM) on the (111) plane suggest dissolution by a residual silicate-carbonate melt. In contrast, polycrystallline character of diamond cuboids (rock 2) along with their common dissolution and formation of numerous tetragonal etch pits reflect relatively rapid growth of these grains from highly supersaturated fluid/melt. Peak P-T conditions for the UHP rocks of ? 1100ºC at 4.5 GPa are located above the phengite dehydration melting curve, where silicate melts are produced and may coexist with carbonate melts. In view of the light carbon isotope composition and lack of carbonates, we suggest that the diamonds crystallized from the graphitized primordial organic matter under reducing conditions at presence of silicate melt.
Compositional variations (major and trace elements) of clinopyroxene and Ti and radite from pyroxenite, ijolite and nepheline syenite, Alno Island, Sweden.
Peltonen, P., Manttari, I., Huhma, H., Whitehouse, M.J.
Multi stage origin of the lower crust of the Karelian craton from 3.5 to 1.7 Ga based on isotopic ages of kimberlite derived mafic granulite xenoliths.
Precambrian Research, Vol. 147, 1-2, June 10, pp. 107-123.
Tichomirowa, M., Whitehouse, M.J., Gerdes, A., Gotze, J., Schulz, B., Belyatsky, B.V.
Different zircon recrystallization types in carbonatites caused by magma mixing: evidence from U-Pb dating, trace element and isotope composition ( Hf and O) of zircons from two Precambrian carbonatites from Fennoscandia.
Abstract: Constraining the origin and history of very ancient detrital zircons has unique potential for furthering our knowledge of Earth's very early crust and Hadean geodynamics. Previous applications of the Ti-in-zircon thermometer to >4 Ga zircons have identified a population with relatively low crystallization temperatures (Tzirxtln) of ?685 °C. This could possibly indicate wet minimum-melting conditions producing granitic melts, implying very different Hadean terrestrial geology from that of other rocky planets. Here we report the first comprehensive ion microprobe study of zircons from a transect through the differentiated Sudbury impact melt sheet (Ontario, Canada). The new zircon Ti results and corresponding Tzirxtln fully overlap with those of the Hadean zircon population. Previous studies that measured Ti in impact melt sheet zircons did not find this wide range because they analyzed samples only from a restricted portion of the melt sheet and because they used laser ablation analyses that can overestimate true Ti content. It is important to note that internal differentiation of the impact melt is likely a prerequisite for the observed low Tzirxtln in zircons from the most evolved rocks. On Earth, melt sheet differentiation is strongest in subaqueous impact basins. Thus, not all Hadean detrital zircon with low Ti necessarily formed during melting at plate boundaries, but at least some could also have crystallized in melt sheets caused by intense meteorite bombardment of the early, hydrosphere-covered protocrust.
Geochimica et Cosmochinica Acta, Vol. 215, pp. 432-446.
Africa, Zimbabwe
craton
Abstract: Hafnium and oxygen isotopic compositions measured in-situ on U-Pb dated zircon from Archaean sedimentary successions belonging to the 2.9–2.8 Ga Belingwean/Bulawayan groups and previously undated Sebakwian Group are used to characterize the crustal evolution of the Zimbabwe Craton prior to 3.0 Ga. Microstructural and compositional criteria were used to minimize effects arising from Pb loss due to metamorphic overprinting and interaction with low-temperature fluids. 207Pb/206Pb age spectra (concordance >90%) reveal prominent peaks at 3.8, 3.6, 3.5, and 3.35 Ga, corresponding to documented geological events, both globally and within the Zimbabwe Craton. Zircon ?18O values from +4 to +10‰ point to both derivation from magmas in equilibrium with mantle oxygen and the incorporation of material that had previously interacted with water in near-surface environments. In ?Hf-time space, 3.8–3.6 Ga grains define an array consistent with reworking of a mafic reservoir (176Lu/177Hf ?0.015) that separated from chondritic mantle at ?3.9 Ga. Crustal domains formed after 3.6 Ga depict a more complex evolution, involving contribution from chondritic mantle sources and, to a lesser extent, reworking of pre-existing crust. Protracted remelting was not accompanied by significant mantle depletion prior to 3.35 Ga. This implies that early crust production in the Zimbabwe Craton did not cause complementary enriched and depleted reservoirs that were tapped by later magmas, possibly because the volume of crust extracted and stabilised was too small to influence (asthenospheric) mantle isotopic evolution. Growth of continental crust through pulsed emplacement of juvenile (chondritic mantle-derived) melts, into and onto the existing cratonic nucleus, however, involved formation of complementary depleted subcontinental lithospheric mantle since the early Archaean, indicative of strongly coupled evolutionary histories of both reservoirs, with limited evidence for recycling and lateral accretion of arc-related crustal blocks until 3.35 Ga.
Abstract: The Tethys margin in central and eastern Asia is comprised of continental terranes separated by suture zones, some of which remain cryptic. Determining the crustal architecture, and therefore the geological history, of the Eastern Tethyan margin remains challenging. Sited in the heart of this region, Myanmar is a highly prospective but poorly explored minerals jurisdiction. A better understanding of Myanmar's mineralization can only be realized through a better understanding of its tectonic history, itself reflected in at least four major magmatic belts. The Eastern and the Main Range Provinces are associated with the Late Permian to Early Triassic closure of Palaeo-Tethys. The Mogok-Mandalay-Mergui Belt and Wuntho-Popa Arc are a response to the Eocene closure of Neo-Tethys. However, magmatic ages outside these two orogenic events are also recorded. We present new zircon U-Pb, Lu-Hf and O isotope data from magmatic rocks across Myanmar, which we append to the existing dataset to isotopically characterize Myanmar's magmatic belts. Eastern Province Permian I-type magmatism has evolved eHf (-10.9 to -6.4), whilst Main Range Province Triassic S-type magmatism also records evolved eHf (-13.5 to -8.8). The Mogok-Mandalay-Mergui Belt is here divided into the Tin Province and the Mogok Metamorphic Belt. The Tin Province hosts ca. 77-50 Ma magmatism with evolved eHf (-1.2 to -15.2), and d 18 O of 5.6-8.3‰. The Mogok Metamorphic Belt exhibits a more complex magmatic and metamorphic history, and granitoids record Jurassic, Late Cretaceous, and Eocene to Miocene phases of magmatism, all of which exhibit evolved eHf values between -4.6 and -17.6, and d 18 O between 6.3 and 9.2‰. From the Tagaung-Myitkyina Belt, we report a magmatic age of 172 Ma and eHf of 18.1 to 10.8. To accommodate the geological evidence, we propose a tectonic model for Myanmar involving a greater Sibumasu - where the documented zircon isotopic variations reflect compositional variations in magmatic source - and invoke the role of a Tengchong Block. The Baoshan Block and Greater Sibumasu were likely assembled on or before the Triassic, a former Andean margin and suture which may lie across the Northern Shan Plateau, and reflected in isotopic differences between the northern and southern parts of the Mogok Metamorphic Belt. This contiguous Sibumasu-Baoshan Block then sutured onto the Indochina margin in the Late Triassic. We propose that a Tengchong Block within Myanmar provides for a southerly termination of the Meso-Tethys suture immediately north of the Mogok area. A discrete Tengchong Block may explain a discontinuous arc of Late Triassic to Jurassic I-type magmatism in central Myanmar, representing an Andean-type margin sited above a subducting Meso-Tethys on the margin of Sibumasu. The Tengchong Block sutured onto Greater Sibumasu before the Late Cretaceous, after which subduction of Neo-Tethys drove the magmatism of the Wuntho-Popa Arc and ultimately that of the Tin Province. The metallogenic character of granite belts in Myanmar reflects the crustal architecture of the region, which is remarkable for its prolific endowment of granite-hosted Sn-W mineralization in two quite distinct granite belts related to sequential Indosinian and Himalayan orogenesis.
Geochimica et Cosmochimica Acta, Vol. 254, pp. 21-39.
New Zealand
metasomatism
Abstract: Megacrystic zircon grains from alkaline basaltic fields are rare but can provide fundamental insights into mantle metasomatic processes. Here, we report in-situ U-Pb ages, trace element concentrations and hafnium and oxygen isotopes for fourteen zircon megacrysts from two intraplate alkaline basalt locations in New Zealand. U-Pb ages indicate the zircons crystallised between 12.1 and 19.8 Ma. Zircon oxygen isotopic compositions range from low to mantle-like compositions (grain average ? ¹? O = 3.8-5.1‰). Hafnium isotopes (?Hf (t) = +3.3 to +10.4) mostly overlap with intraplate mafic rocks and clinopyroxene in metasomatized peridotitic mantle xenoliths but show no correlation with most trace element parameters or oxygen isotopes. The zircons are interpreted to have formed by the reaction between low-degree melts derived from pre-existing mantle metasomes and the depleted mantle lithosphere prior to eruption and transport to the surface. The low Hf concentration, an absence of Eu anomalies, and elevated U/Yb compared to Nb/Yb in the megacrystic zircons are interpreted to show that the source metasomes comprised subduction- and carbonatite-metasomatised lithospheric mantle. As these trace element characteristics are common for megacrystic zircon in intra-plate basaltic fields globally, they suggest the prevalence of subduction- and carbonatite-metsasomatised mantle under these intraplate volcanic regions. The unusually low ? ¹? O was likely present prior to metasomatic enrichment and may have resulted from high-temperature hydrothermal alteration during initial mantle lithosphere formation at a mid ocean ridge or, possibly, during subduction-related processes associated with continent formation. The combination of proportionally varied contributions from carbonatite- and subduction-metasomatised lithospheric melts with asthenospheric melts may explain the variety of primitive intraplate basalt compositions, including low ? ¹? O reported for some local intraplate lavas.
Tsuji, L.J.S., McCarthy, D.D., Whitelaw, G.S., McEachren, J.
Getting back to basics: the Victor diamond mine environmental assessment scoping process and the issue of family based traditional lands versus reg. traplines
Impact assessment and Project Appraisal, March Vol. 29, no. 1, pp. 37-47.
Skeleton, A., Whitmarsh, R., Arghe, F., Crill, P., Koyi, H.
Constraining the rate and extent of mantle serpentinization from seismic and petrological data: implications for chemosynthesis and tectonic processes.
Skelton, A., Whitmarsh, R., Arghe, F., Crill, P., Koyi, H.
Constraining the rate and extent of mantle serpentinization from seismic and petrological data: implications for chemosynthesis and tectonic processes.
Geosphere via Researchgate, Vol. 3, 4, pp. 220-259.
Canada, United States
craton
Abstract: This paper presents a plate-scale model for the Precambrian growth and evolution of the North American continent. The core of the North American continent (Canadian shield) came together in the Paleoproterozoic (2.0-1.8 Ga) by plate collisions of Archean continents (Slave with Rae-Hearne, then Rae-Hearne with Superior) as well as smaller Archean continental fragments (Wyoming, Medicine Hat, Sask, Marshfield, Nain cratons). The resulting Trans-Hudson orogen was a collisional belt similar in scale to the modern Himalayas. It contains mainly reworked Archean crust, but remnants of juvenile volcanic belts are preserved between Archean masses. The thick, buoyant, and compositionally depleted mantle lithosphere that now underlies North America, although dominantly of Archean age, took its present shape by processes of collisional orogenesis and likely has a scale of mantle heterogeneity similar to that exhibited in the overlying crust. In marked contrast, lithosphere of southern North America (much of the conti nental United States) was built by progressive addition of a series of dominantly juvenile vol canic arcs and oceanic terranes accreted along a long-lived southern (present coordinates) plate margin. Early juvenile additions (Pembine-Wausau, Elves Chasmarcs) formed at the same time (1.84-1.82 Ga) the core was assembling. Following final assembly of the Archean and Paleoproterozoic core of North America by 1.8 Ga, major accretionary provinces (defined mainly by isotopic model ages) were added by arc-continent accretion, analogous to present-day convergence between Australia and Indonesia. Also similar to Indonesia, some accreted terranes contain older continental crustal material [Archean(?) Mojavia], but the extent and geometry of older crust are not well known. Accretionary provinces are composed of numerous 10 to 100 km scale terranes or blocks, separated by shear zones, some of which had compound histories as terrane sutures and later crustal-assembly structures. Major northeast-trending provinces are the Yavapai province (1.80-1.70 Ga), welded to North America during the 1.71-1.68 Ga Yavapai orogeny; the Mazatzal province (1.70-1.65 Ga), added during the 1.65-1.60 Ga Mazatzal orogeny; the Granite-Rhyolite province (1.50-1.30 Ga), added during the 1.45-1.30 Ga tectonic event associated with A-type intracratonic magmatism; and the Llano-Grenville province (1.30-1.00 Ga), added during the 1.30-0.95 Ga broader Grenville orogeny. During each episode of addition of juvenile lithosphere, the transformation of juvenile crust into stable continental lithosphere was facilitated by voluminous granitoid plutonism that stitched new and existing orogenic boundaries. Slab roll back created transient extensional basins (1.70 and 1.65 Ga) in which Paleoproterozoic quartzite-rhyolite successions were deposited, then thrust imbricated as basins were inverted. The lithospheric collage that formed from dominantly juvenile terrane accretion and stabilization (1.8-1.0 Ga) makes up about half of the present-day North American continent. Throughout (and as a result of) this long-lived convergent cycle, mantle lithosphere below the accretionary provinces was more hydrous, fertile, and relatively weak compared to mantle lithosphere under the Archean core.
An open source software environment for visualizing and refining plate tectonic reconstructions using high resolution geological and geophysical dat a sets.
Strain heating as a mechanism for partial melting and ultrahigh temperature metamorphism in convergent orogens: implications of temperature dependent thermal
Journal of Geophysical Research, Vol. 115, B 12 B12417
International Journal of earth Sciences, Vol. 110, pp. 1593-1609.
Canada, Ontario
carbonatite
Abstract: Igneous intrusions are important to the thermomechanical evolution of continents because they inject heat into their relatively cold host rocks, and potentially change the distribution of radiogenic heat production and thermal properties within the crust. To explore one aspect of the complex evolution of the continental crust, this paper investigates the local thermal effects of two intrusive rock types (carbonatites and anorthosites) on the Archean Superior Province of the Canadian shield. We provide new data on their contrasting properties: rock density near 298 K, thermal diffusivity, and heat capacity up to 800 K (which altogether yield thermal conductivity), plus radiogenic element contents. The volumetrically small carbonatites have widely varying radiogenic heat production (2–56 µW m?3) and moderate thermal conductivity at 298 K (~?1 to 4 W m?1 K?1) which decreases with temperature. The massive Shawmere anorthosite has nearly negligible radiogenic heat production (
Mineralium Deposita, 10.1007/s00126-020-01026-z 20p. Pdf
Australia
REE
Abstract: The Yangibana rare earth element (REE) district consists of multiple mineral deposits/prospects hosted within the Mesoproterozoic Gifford Creek Carbonatite Complex (GCCC), Western Australia, which comprises a range of rock types including calcite carbonatite, dolomite carbonatite, ankerite-siderite carbonatite, magnetite-biotite dykes, silica-rich alkaline veins, fenite, glimmerites and what have historically been called “ironstones”. The dykes/sills were emplaced during a period of extension and/or transtension, likely utilising existing structures. The Yangibana REE deposits/prospects are located along many of these structures, particularly along the prominent Bald Hill Lineament. The primary ore mineral at Yangibana is monazite, which is contained within ankerite-siderite carbonatite, magnetite-biotite dykes and ironstone units. The ironstones comprise boxwork-textured Fe oxides/hydroxides, quartz, chalcedony and minor monazite and subordinate rhabdophane. Carbonate mineral-shaped cavities in ironstone, fenite and glimmerite alteration mantling the ironstone units, and ankerite-siderite carbonatite dykes altering to ironstone-like assemblages in drill core indicate that the ironstones are derived from ankerite-siderite carbonatite. This premise is further supported by similar bulk-rock Nd isotope composition of ironstone and other alkaline igneous rocks of the GCCC. Mass balance evaluation shows that the ironstones can be derived from the ankerite-siderite carbonatites via significant mass removal, which has resulted in passive REE concentration by ~?2 to ~?10 times. This mass removal and ore tenor upgrade is attributed to extensive carbonate breakdown and weathering of ankerite-siderite carbonatite by near-surface meteoric water. Monazite from the ironstones has strong positive and negative correlations between Pr and Nd, and Nd and La, respectively. These relationships are reflected in the bulk-rock drill assays, which display substantial variation in the La/Nd throughout the GCCC. The changes in La/Nd are attributed to variations in primary magmatic composition, shifts in the magmatic-hydrothermal systems related to CO2 versus water-dominated fluid phases, and changes in temperature.
Earth & Environment Communications, 10.1038/s43247-021-00145-3 16p. Pdf
United States, Hawaii
magmatism
Abstract: Volcanoes represent one of the largest natural sources of metals to the Earth’s surface. Emissions of these metals can have important impacts on the biosphere as pollutants or nutrients. Here we use ground- and drone-based direct measurements to compare the gas and particulate chemistry of the magmatic and lava-seawater interaction (laze) plumes from the 2018 eruption of K?lauea, Hawai’i. We find that the magmatic plume contains abundant volatile metals and metalloids whereas the laze plume is further enriched in copper and seawater components, like chlorine, with volatile metals also elevated above seawater concentrations. Speciation modelling of magmatic gas mixtures highlights the importance of the S2? ligand in highly volatile metal/metalloid degassing at the magmatic vent. In contrast, volatile metal enrichments in the laze plume can be explained by affinity for chloride complexation during late-stage degassing of distal lavas, which is potentially facilitated by the HCl gas formed as seawater boils.
Society of Economic Geology Geoscience and Exploration of the Argyle, Bunder, Diavik, and Murowa Diamond Deposits, Special Publication no. 20, pp. 169-190.
Yellowknife Forum NWTgeoscience.ca, abstract volume poster p. 123-124.
Canada, Northwest Territories
deposit - Kelvin
Abstract: Research at the Kelvin kimberlite, NWT, is defining surface exploration practices and testing new host rock lithogeochemical exploration tools that will result in reduced costs and improved discovery success. In regions where recent glaciation has buried kimberlites under glacial sediments, surface geochemical detection methods are best interpreted when coupled with a comprehension of the landscape formation processes. The glacial, post-glacial, and cryoturbation processes that have affected the landscape have, in turn, affected the dispersal of geochemical signatures in the till that can be detected and exploited by detailed surface mapping, sampling, and geochemical analysis. The Kelvin kimberlite is an inclined pipe that subcrops from metaturbidite country rock beneath a lake. No indicator mineral train has been detected at Kelvin by traditional indicator mineral methods. Relative uniformity of surficial material (<6m thick till blanket) allows for extensive B horizon soil sampling above the kimberlite, up-ice, and up to 1 km down-ice. Four acid and aqua regia ICP-MS results of the -180 ?m fraction indicate the presence of subtle pathfinder element trains originating from the kimberlite subcrop location and extending for >1km down-ice. Dry sonic sieving and four acid digestion results provide interpretations of geochemical partitioning and the ideal size fraction for geochemical sampling. Trace elements demonstrate systematically elevated concentrations in the fine and very fine silt fractions; however, background is higher and anomalous to background contrast is not enhanced compared to bulk -180 ?m ratios. Elevated pathfinder concentrations in the fine to very fine sand fraction are attributed to fine kimberlite indicator minerals and their fragments, and display the best anomalous to background contrast ratio. Whole soil commercial Pb isotope analysis of select soils provide supplemental data to fingerprint the petrogenetic source of anomalous samples. Additional research is being carried out to detect alteration signatures in the country rock induced by the emplacement of the kimberlite. Lithogeochemical data from four drill holes aims to identify and quantify the metasomatic enrichment and depletion of elements sourced from the kimberlite, while hyperspectral imaging will aim to detect secondary mineralogy and subtle changes in mineral composition. This data will be used to generate mineralogical and geochemical vectors beneficial in near-miss situations when drilling kimberlites and defining diatreme geometries.
Till geochemistry and lithogeochemical exploration for a concealed kimberlite.
2018 Yellowknife Geoscience Forum , p. 88-89. abstract
Canada, Northwest Territories
deposit - Kelvin
Abstract: Research at the Kelvin kimberlite, NWT is defining surface exploration practices and developing new exploration tools based on host rock lithogeochemical alteration, that will result in reduced costs and improved discovery success. In regions where recent glaciation has buried kimberlites under glacial sediments, surface geochemical detection methods are best interpreted when coupled with a comprehension of the landscape formation processes. The glacial, post-glacial, and cryoturbation processes that have affected the landscape have, in turn, affected the dispersal of geochemical signatures in the till that can be detected and exploited by detailed surface mapping, sampling, and geochemical analysis. Additionally, the application of geochemical and hyperspectral data to country rock alteration core can aid in the detection of kimberlites during near-miss drilling campaigns. The Kelvin kimberlite is located eight kilometers from the Gahcho Kué diamond mine in the Northwest Territories. The inclined pipe sub-crops beneath a lake and dips into gneiss country rock towards the northwest with a surface projection of more than 600 m long. Relative uniformity of surficial material (<6 m thick till veneer) allows for extensive b-horizon soil sampling above the kimberlite, up-ice, and up to 1 km in the down-ice direction. Samples were sieved to -180 microns and analyzed by four acid digest ICP-MS and aqua-regia digest ICP-MS. Results indicate the soils to be very immature and identify the presence of a subtle Ni-Cr-Mg-Nb train originating from the lake side extending for >1km from source following the most recent ice direction to the west. The material for the train was abraded by the ice from the kimberlite, now sub-cropping beneath a lake, and would have provided additional support to drill what was initially targeted from geophysics. Additional research is being carried out to detect alteration signatures in the country rock induced by the emplacement of the kimberlite. Lithogeochemical data from four drill holes aims to identify and quantify the metasomatic enrichment and depletion of elements sourced from the kimberlite while accounting for country-rock lithology variation. Hyperspectral imaging of the same drill core will aim to detect and quantify secondary mineralogy and subtle changes in mineral composition that otherwise cannot be detected visually. This data will be used to generate mineralogical and chemical vectors beneficial in near-miss situations when drilling kimberlites and defining diatreme geometries.
Geophysics Research Letters, Vol. 44, 5, pp. 2148-2158.
Mantle
geophysics - seismics
Abstract: We explore the effect of Mg/Fe substitution on the sound velocities of iron-rich (Mg1 ? xFex)O, where x = 0.84, 0.94, and 1.0. Sound velocities were determined using nuclear resonance inelastic X-ray scattering as a function of pressure, approaching those of the lowermost mantle. The systematics of cation substitution in the Fe-rich limit has the potential to play an important role in the interpretation of seismic observations of the core-mantle boundary. By determining a relationship between sound velocity, density, and composition of (Mg,Fe)O, this study explores the potential constraints on ultralow-velocity zones at the core-mantle boundary.
Deijanin, B., Simic, D., Zaitsev, A., Chapman, J., Dobrinets, I., Widemann, A., Del Re, N., Middleton, T., Dijanin, E., Se Stefano, A.
Characterization of pink diamonds of different origin: natural ( Argyle, non-Argyle), irradiated and annealed, treated with multi-process, coated and synthetic.
Diamond and Related Materials, Vol. 17, 7-10, pp. 1169-1178.
Yang, J.S., Wirth, R., Wiedenbeck, M., Griffin, W.L., Meng, F.C., Chen, S.Y., Bai, W.J., Xu, X.X., Makeeyev, A.B., Bryanchaniniova, N.I.
Diamonds and highly reduced minerals from chromitite of the Ray-Iz ophiolite of the Polar Urals: deep origin of podiform chromitites and ophiolitic diamonds.
Nature Communications, Jan. 31, doi 10:1038/ncomms1048
Africa, Mauritius
Hot spots
Abstract: A fragment of continental crust has been postulated to underlie the young plume-related lavas of the Indian Ocean island of Mauritius based on the recovery of Proterozoic zircons from basaltic beach sands. Here we document the first U-Pb zircon ages recovered directly from 5.7?Ma Mauritian trachytic rocks. We identified concordant Archaean xenocrystic zircons ranging in age between 2.5 and 3.0?Ga within a trachyte plug that crosscuts Older Series plume-related basalts of Mauritius. Our results demonstrate the existence of ancient continental crust beneath Mauritius; based on the entire spectrum of U-Pb ages for old Mauritian zircons, we demonstrate that this ancient crust is of central-east Madagascar affinity, which is presently located ?700?km west of Mauritius. This makes possible a detailed reconstruction of Mauritius and other Mauritian continental fragments, which once formed part of the ancient nucleus of Madagascar and southern India.
Abstract: The Cameca 1280-HR large geometry SIMS instrument is a highly versatile analytical tool which can support a broad range of geochemical applications. Research using the Potsdam 1280 instrument focuses primarily on isotope ratio determinations in geomaterials. Optimized measurement protocols have already been established for ?18O determinations in zircon, and we are also working towards routine oxygen isotope determinations for quartz, calcite, mica, apatite and titanite. The primary challenge in developing such measurement systems are the identification and characterization of suitable reference materials (RMs), and this is made particularly challenging due to the matrix dependent ion yields of the SIMS ion source. Here we wish to report our progress towards establishing new analytical protocols for the determination of ?13C in both diamond and moissanite. In the case of diamond, our facility possesses three natural RMs with which we are able to produce data with a typical analytical repeatability of ?0.15 ‰ (1sd). An inter-comparison of our three diamond RMs demonstrates an overall data quality of better than 0.5‰ in terms of systematic offset between the various materials characterized using gas source mass spectrometry (Palot et al., 2012). A single such ?13C determination in diamond requires 80 s of data acquisition and involves a test portion mass of ?400 pg of material. In-house diamond reference materials for ?15N calibration allow us to measure this isotopic system to a total analytical uncertainty of ± 1.6 ‰ (1sd) at nitrogen concentrations reaching down to 250 ?g/g. Due to the relatively low abundance of nitrogen in diamonds, such isotope ratio determinations require around 9 minutes of data collection. With respect to ?13C determinations in moissanite, we use a kimberlitic SiC as calibrant (Mathez et al., 1995), on which we achieve a repeatability of ?0.2 ‰ (1sd) on a ?350 pg test portion mass. Total data acquisition time for such measurements is 80 s. We are currently in the process of developing a second moissanite RM based on a synthetic, coarse-grained powder. We will also investigate this new material for its ?30Si characteristics.
Reutsky, V.N., Shiryaev, A.A., Titkov, S.V., Wiedenbeck, M., Zudina, N.N.
Evidence for large scale fractionation of carbon isotopes and of nitrogen impurity during crystallization of gem quality cubic diamonds from placers of North Yakutia.
Geochemistry International, Vol. 55, 11, pp. 988-999.
Russia, Yakutia
alluvials
Abstract: The spatial distribution of carbon and nitrogen isotopes and of nitrogen concentrations is studied in detail in three gem quality cubic diamonds of variety II according to Orlov’s classification. Combined with the data on composition of fluid inclusions our results point to the crystallization of the diamonds from a presumably oxidized carbonate fluid. It is shown that in the growth direction ?13C of the diamond becomes systematically lighter by 2-3‰ (from -13.7 to -15.6‰ for one profile and from -11.7 to -14.1‰ for a second profile). Simultaneously, we observe substantial decrease in the nitrogen concentration (from 400-1000 to 10-30 at ppm) and a previously unrecognized enrichment of nitrogen in light isotope, exceeding 30‰. The systematic and substantial changes of the chemical and isotopic composition can be explained using the Burton-Prim-Slichter model, which relates partition coefficients of an impurity with the crystal growth rate. It is shown that changes in effective partition coefficients due to a gradual decrease in crystal growth rate describes fairly well the observed scale of the chemical and isotopic variations if the diamond-fluid partition coefficient for nitrogen is significantly smaller than unity. This model shows that nitrogen isotopic composition in diamond may result from isotopic fractionation during growth and not reflect isotopic composition of the mantle fluid. Furthermore, it is shown that the infra-red absorption at 1332 ?m-1 is an integral part of the Y-defect spectrum. In the studied natural diamonds the 1290 ?m-1 IR absorption band does not correlate with boron concentration.
South African Journal of Geology, Vol. 120, 3, pp. 371-384.
Africa, Zimbabwe, South Africa
diamond morphology
Abstract: The morphological, chemical impurities and carbon isotope properties of diamonds may reveal subtle details of their mantle source and growth characteristics, supporting efforts towards identifying their original place of harvesting. Here we investigate the mantle carbon and nitrogen sources and growth patterns from selected diamonds mined from four kimberlites: macro-sized diamonds from River Ranch kimberlite in Zimbabwe and the Swartruggens and Klipspringer kimberlitic deposits from South Africa, and micro-sized diamonds from the Klipspringer and Premier kimberlite intrusions in South Africa. Type IaAB diamonds are found in all the samples; Type IaB diamonds only occur in samples from the Swartruggens, River Ranch and Premier kimberlites. A single Type II diamond (nitrogen below the detection limit) was also observed in the River Ranch and Premier kimberlites. Both the micro- and macro-sized diamonds from Klipspringer have similar nitrogen contents. Based on the % B-defect, the diamonds from Klipspringer are grouped into low- and high-nitrogen aggregates (i.e. % of B-defect <40% and >56%, respectively) that likely represent two different diamond forming episodes. Time averaged mantle storage temperatures for Type IaAB diamonds are calculated to have been: 1060°C for Swartruggens; 1190°C for River Ranch; 1100°C (low aggregated); and 1170°C (highly aggregated) for Klipspringer, and 1210°C for Premier diamonds. The CL-images of the River Ranch, Klipspringer and Premier diamonds reveal multi-oscillatory growth zones. The carbon isotopic analyses on the diamonds reveal an average ?13CVPDB value of: -4.5‰ for Swartruggens; -4.7‰ for River Ranch; -4.5‰ for Klipspringer; and -3‰ for Premier. With the exception of the diamond from Premier, the average ?13C value of the diamonds are similar to the average ?13C value of the mantle (-5‰), which is similar to the occurrence of diamonds in the other kimberlites. The internal carbon isotopic variation of individual diamonds from Swartruggens, Klipspringer and Premier are less than 4‰, which is similar to the variability of most other diamond occurrences reported from elsewhere in the world. Up to 6.7‰ internal carbon isotopic variation was observed in a single diamond from River Ranch. The internal carbon isotopic studies of the diamonds reveal that the primary carbon in the Swartruggens and Klipspringer was derived from an oxidation of CH4-bearing fluid, whereas in the River Ranch the primary carbon was derived from the reduction of carbonate-or CO2-bearing fluids. The Swartruggens diamonds also reveal a secondary carbon sourced from a reduction of CO2- or carbonate-rich fluid or melt. Diamonds from Klipspringer exhibit a cyclic change in ?13C values that reflects fluctuation in a complex mantle perturbation system or periodic change in fugacity of the mantle. Based on this study, we conclude that, in principle, a selected range of diamond signatures might be used to fingerprint their origins; especially when linked to their other physical properties such as a low temperature magnetic signature.
Earth and Planteray Science Letters, Vol. 488, pp. 134-143.
Mantle
nitrogen
Abstract: The solubility of nitrogen in the major minerals of the Earth's transition zone and lower mantle (wadsleyite, ringwoodite, bridgmanite, and Ca-silicate perovskite) coexisting with a reduced, nitrogen-rich fluid phase was measured. Experiments were carried out in multi-anvil presses at 14 to 24 GPa and 1100 to 1800?°C close to the Fe-FeO buffer. Starting materials were enriched in 15N and the nitrogen concentrations in run products were measured by secondary ion mass spectrometry. Observed nitrogen (15N) solubilities in wadsleyite and ringwoodite typically range from 10 to 250 ?g/g and strongly increase with temperature. Nitrogen solubility in bridgmanite is about 20 ?g/g, while Ca-silicate perovskite incorporates about 30 ?g/g under comparable conditions. Partition coefficients of nitrogen derived from coexisting phases are DNwadsleyite/olivine = 5.1 ± 2.1, DNringwoodite/wadsleyite = 0.49 ± 0.29, and DNbridgmanite/ringwoodite = 0.24 . Nitrogen solubility in the solid, iron-rich metal phase coexisting with the silicates was also measured and reached a maximum of nearly 1 wt.% 15N at 23 GPa and 1400?°C. These data yield a partition coefficient of nitrogen between iron metal and bridgmanite of DNmetal/bridgmanite???98, implying that in a lower mantle containing about 1% of iron metal, about half of the nitrogen still resides in the silicates. The high nitrogen solubility in wadsleyite and ringwoodite may be responsible for the low nitrogen concentrations often observed in ultradeep diamonds from the transition zone. Overall, the solubility data suggest that the transition zone and the lower mantle have the capacity to store at least 33 times the mass of nitrogen presently residing in the atmosphere. By combining the nitrogen solubility data in minerals with data on nitrogen solubility in silicate melts, mineral/melt partition coefficients of nitrogen can be estimated, from which the behavior of nitrogen during magma ocean crystallization can be modeled. Such models show that if the magma ocean coexisted with a primordial atmosphere having a nitrogen partial pressure of just a few bars, several times the current atmospheric mass of nitrogen must have been trapped in the deep mantle. It is therefore plausible that the apparent depletion of nitrogen relative to other volatiles in the near-surface reservoirs reflects the storage of a larger reservoir of nitrogen in the solid Earth. Dynamic exchange between these reservoirs may have induced major fluctuations of bulk atmospheric pressure over Earth's history.
Contributions to Mineralogy and Petrology, doi.org:10.1007/ s00410-018-1499-5 19p.
Europe, Turkey
diamond inclusions
Abstract: The Pozanti-Karsanti ophiolite (PKO) is one of the largest oceanic remnants in the Tauride belt, Turkey. Micro-diamonds were recovered from the podiform chromitites, and these diamonds were investigated based on morphology, color, cathodoluminescence, nitrogen content, carbon and nitrogen isotopes, internal structure and inclusions. The diamonds recovered from the PKO are mainly mixed-habit diamonds with sectors of different brightness under the cathodoluminescence images. The total ?13C range of the PKO diamonds varies between ? 18.8 and ? 28.4‰, with a principle ?13C mode at ? 25‰. Nitrogen contents of the diamonds range from 7 to 541 ppm with a mean value of 171 ppm, and the ?15N values range from ? 19.1 to 16.6‰, with a ?15N mode of ? 9‰. Stacking faults and partial dislocations are commonly observed in the Transmission Electron Microscopy foils whereas inclusions are rather rare. Combinations of ( Ca0.81Mn0.19)SiO3, NiMnCo-alloy and nanosized, quenched fluid phases were observed as inclusions in the PKO diamonds. We believe that the 13C-depleted carbon signature of the PKO diamonds derived from previously subducted crustal matter. These diamonds may have crystallized from C-saturated fluids in the asthenospheric mantle at depth below 250 km which were subsequently carried rapidly upward by asthenospheric melts.
Geochemistry International, Vol. 56, 13, pp. 1398-1404.
Global
diamond morphology
Abstract: We report the carbon isotope compositions of a set of diamond crystals recovered from an investigation of the experimental interaction of metal iron with Mg-Ca carbonate at high temperature and high pressure. Despite using single carbon source with ?13C equal to +0.2‰ VPDB, the diamond crystals show a range of ?13C values from -0.5 to -17.1‰ VPDB. Diamonds grown in the metal-rich part of the system are relatively constant in their carbon isotope compositions (from -0.5 to -6.2‰), whereas those diamonds recovered from the carbonate dominated part of the capsule show a much wider range of ?13C (from -0.5 to -17.1‰). The experimentally observed distribution of diamond’ ?13C using a single carbon source with carbon isotope ratio of marine carbonate is similar to that found in certain classes of natural diamonds. Our data indicate that the ?13C distribution in diamonds that resulted from a redox reaction of marine carbonate with reduced mantle material is hardly distinguishable from the ?13C distribution of mantle diamonds.
Geochemistry International, Vol. 55, 11, pp. 988-999.
Russia, Yakutia
diamond morphology
Abstract: The spatial distribution of carbon and nitrogen isotopes and of nitrogen concentrations is studied in detail in three gem quality cubic diamonds of variety II according to Orlov’s classification. Combined with the data on composition of fluid inclusions our results point to the crystallization of the diamonds from a presumably oxidized carbonate fluid. It is shown that in the growth direction ?13C of the diamond becomes systematically lighter by 2-3‰ (from -13.7 to -15.6‰ for one profile and from -11.7 to -14.1‰ for a second profile). Simultaneously, we observe substantial decrease in the nitrogen concentration (from 400-1000 to 10-30 at ppm) and a previously unrecognized enrichment of nitrogen in light isotope, exceeding 30‰. The systematic and substantial changes of the chemical and isotopic composition can be explained using the Burton-Prim-Slichter model, which relates partition coefficients of an impurity with the crystal growth rate. It is shown that changes in effective partition coefficients due to a gradual decrease in crystal growth rate describes fairly well the observed scale of the chemical and isotopic variations if the diamond-fluid partition coefficient for nitrogen is significantly smaller than unity. This model shows that nitrogen isotopic composition in diamond may result from isotopic fractionation during growth and not reflect isotopic composition of the mantle fluid. Furthermore, it is shown that the infra-red absorption at 1332 ?m-1 is an integral part of the Y-defect spectrum. In the studied natural diamonds the 1290 ?m-1 IR absorption band does not correlate with boron concentration.
Abstract: Isotopic and trace element variations within single diamond crystals are widely known from both natural stones and synthetic crystals. A number of processes can produce variations in carbon isotope composition and nitrogen abundance in the course of diamond crystallization. Here, we present evidence of carbon and nitrogen fractionation related to the growing surfaces of a diamond. We document that difference in the carbon isotope composition between cubic and octahedral growth sectors is solvent-dependent and varies from 0.7h in a carbonate system to 0.4h in a metal-carbon system. Ab initio calculations suggest up to 4h instantaneous 13C depletion of cubic faces in comparison to octahedral faces when grown simultaneously. Cubic growth sectors always have lower nitrogen abundance in comparison to octahedral sectors within synthetic diamond crystals in both carbonate and metal-carbon systems. The stability of any particular growth faces of a diamond crystal depends upon the degree of carbon association in the solution. Octahedron is the dominant form in a high-associated solution while the cube is the dominant form in a low-associated solution. Fine-scale data from natural crystals potentially can provide information on the form of carbon, which was present in the growth media.
Abstract: Cuboid diamonds are particularly common in the placers of the northeastern Siberian platform, but their origin remains unclear. These crystals usually range in color from dark yellow to orange and, more interestingly, are characterized by unusual low aggregated nitrogen impurities (non-aggregated C-center), suggesting a short residence time and/or low temperatures at which they have been stored in the mantle. In order to track possible isotopic signature that could help deciphering cuboid diamond’s crystallization processes, ?¹³C values, ?¹?N values, and nitrogen concentrations have been determined in situ in three samples using secondary ion mass spectrometry (SIMS), whereas nitrogen aggregation states have been determined by FTIR spectroscopy. The samples fall out of the ?¹³C vs. ?¹?N field of canonical mantle composition. Different scales of carbon and nitrogen fractionation may produce the observed variations. Alternatively, mixing mantle and crustal material would obscure initial co-variations of ?¹³C values with ?¹?N or nitrogen content.
Earth and Planetary Science Letters, Vol. 482, pp. 556-566.
Mantle
nitrogen
Abstract: Understanding the evolution of nitrogen (N) across Earth's history requires a comprehensive understanding of N's behaviour in the Earth's mantle - a massive reservoir of this volatile element. Investigation of terrestrial N systematics also requires assessment of its evolution in the Earth's atmosphere, especially to constrain the N content of the Archaean atmosphere, which potentially impacted water retention on the post-accretion Earth, potentially causing enough warming of surface temperatures for liquid water to exist. We estimated the proportion of recycled N in the Earth's mantle today, the isotopic composition of the primitive mantle, and the N content of the Archaean atmosphere based on the recycling rates of N in modern-day subduction zones. We have constrained recycling rates in modern-day subduction zones by focusing on the mechanism and efficiency of N transfer from the subducting slab to the sub-arc mantle by both aqueous fluids and slab partial melts. We also address the transfer of N by aqueous fluids as per the model of Li and Keppler (2014). For slab partial melts, we constrained the transfer of N in two ways - firstly, by an experimental study of the solubility limit of N in melt (which provides an upper estimate of N uptake by slab partial melts) and, secondly, by the partitioning of N between the slab and its partial melt. Globally, 45-74% of N introduced into the mantle by subduction enters the deep mantle past the arc magmatism filter, after taking into account the loss of N from the mantle by degassing at mid-ocean ridges, ocean islands and back-arcs. Although the majority of the N in the present-day mantle remains of primordial origin, our results point to a significant, albeit minor proportion of mantle N that is of recycled origin (% or % of N in the present-day mantle has undergone recycling assuming that modern-style subduction was initiated 4 or 3 billion years ago, respectively). This proportion of recycled N is enough to cause a departure of N isotopic composition of the primitive mantle from today's N of ?5‰ to ‰ or ‰. Future studies of Earth's parent bodies based on the bulk Earth N isotopic signature should take into account these revised values for the N composition of the primitive mantle. Also, the Archaean atmosphere had a N partial pressure of 1.4-1.6 times higher than today, which may have warmed the Earth's surface above freezing despite a faint young Sun.
Abstract: Coupled oxygen-hafnium isotope and trace element geochemical data were obtained using thirty eight previously dated zircon grains extracted from five mafic to intermediate crustal xenoliths of the Wyoming Craton (Montana, USA). Xenoliths include mid to lower crustal (642-817?°C and 3.5-9.4?kbar) mafic granulites and amphibolites with dominantly Mesoproterozoic (1772-1874?Ma) and minor Paleoproterozoic to Late Archean (2004-2534?Ma) 207Pb/206Pb zircon ages. Zircon oxygen isotope data indicate derivation from melts in equilibrium with a mantle source that interacted with limited supracrustal material (?18O?=?4.4-5.7‰), as well as the incorporation of supracrustal fluids or melts into mantle source regions (?18O?=?6.0-8.1‰). The small within-sample isotopic variability suggests that primary zircon did not exchange with isotopically distinct fluids or melts after initial formation. Initial zircon Hf isotopic values are highly variable across all xenoliths (?Hf?=?+3.7 to ?17.6), consistent with protolith derivation from mantle sources that incorporated evolved, unradiogenic material or were modified by subduction-related fluids. Within a single granulite xenolith, two zircon types are recognized based on CL imagery, Hf isotopes and U-Pb ages (Type I and Type II). Type I magmatic zircons show dispersed ages (ca. 1700-2534?Ma) and unradiogenic initial Hf (?Hf?=??17.6 to ?1.5, 176Hf/177Hf?=?0.281074-0.281232). The spread in ages and initial ?Hf, but narrow range in initial 176Hf/177Hf, points to variable Pb loss in response to dissolution-recrystallization of pre-existing zircon. Type II metamorphic zircon yields a younger Proterozoic population (ca. 1700-2155?Ma) with more radiogenic initial Hf relative to Type I zircon (?Hf?=??7.9 to +1.4, 176Hf/177Hf?=?0.281427-0.281578); this type represents newly grown metamorphic zircon that formed in the solid-state and incorporated Zr and Hf from pre-existing zircon and silicate matrix/metamorphic phases. REE patterns from all xenoliths are steep and positively sloping without discernible HREE depletion relative to LREE, implying zircon crystallization/recrystallization in the absence of garnet. Negative Eu anomalies signify simultaneous zircon and feldspar crystallization. Solid-state recrystallization may have lead to variations in LREE, Eu and Ce in certain xenoliths. Xenoliths containing magmatic zircon (1834?±?19?Ma) with mantle-like ?18O (4.4-5.5‰) and radiogenic initial ?Hf (?2.3 to +3.7) likely formed through crystallization of melts derived from a mantle source that incorporated minor amounts of subducted sedimentary/supracrustal material. Proterozoic (1874?±?8?Ma) xenoliths with elevated ?18O (6.0-7.0‰) and unradiogenic initial ?Hf (?8.2 to ?9.6) within magmatic zircon represent melt products of subduction-induced melting and metasomatism of the overlying mantle wedge in the vicinity of the northern GFTZ. Older (ca. 2534?Ma) xenoliths containing zircons with elevated ?18O (6.4-7.2‰) and unradiogenic ?Hf (up to ?17.6) represent crystallization of protolith magmas extracted from a mantle source metasomatized by subduction-derived fluids and melts in the Late Archean or earlier. Zircon geochronology and isotope systematics within Mesoproterozoic xenoliths support a model of ocean-closure and subsequent continental collision between the Medicine Hat Block and Wyoming Craton, resulting in the formation of subduction-related melts at ca. 1834-1874?Ma, followed by ca. 1770?Ma collision-related metamorphism thereafter.
Geochemistry International, Vol. 56, 13, pp. 1398-1404.
Mantle
redox
Abstract: We report the carbon isotope compositions of a set of diamond crystals recovered from an investigation of the experimental interaction of metal iron with Mg-Ca carbonate at high temperature and high pressure. Despite using single carbon source with ?13C equal to +0.2‰ VPDB, the diamond crystals show a range of ?13C values from -0.5 to -17.1‰ VPDB. Diamonds grown in the metal-rich part of the system are relatively constant in their carbon isotope compositions (from -0.5 to -6.2‰), whereas those diamonds recovered from the carbonate dominated part of the capsule show a much wider range of ?13C (from -0.5 to -17.1‰). The experimentally observed distribution of diamond’ ?13C using a single carbon source with carbon isotope ratio of marine carbonate is similar to that found in certain classes of natural diamonds. Our data indicate that the ?13C distribution in diamonds that resulted from a redox reaction of marine carbonate with reduced mantle material is hardly distinguishable from the ?13C distribution of mantle diamonds.
Abstract: We investigated emerald, the bright-green gem variety of beryl, from a new locality at Kruta Balka, Ukraine, and compare its chemical characteristics with those of emeralds from selected occurrences worldwide (Austria, Australia, Colombia, South Africa, Russia) to clarify the types and amounts of substitutions as well as the factors controlling such substitutions. For selected crystals, Be and Li were determined by secondary ion mass spectrometry, which showed that the generally assumed value of 3 Be atoms per formula unit (apfu) is valid; only some samples such as the emerald from Kruta Balka deviate from this value (2.944 Be apfu). An important substitution in emerald (expressed as an exchange vector with the additive component Al2Be3Si6O18) is (Mg,Fe2+)NaAl1?1, leading to a hypothetical end-member NaAl(Mg,Fe2+)[Be3Si6O18] called femag-beryl with Na occupying a vacancy position (?) in the structural channels of beryl. Based on both our results and data from the literature, emeralds worldwide can be characterized based on the amount of femag-substitution. Other minor substitutions in Li-bearing emerald include the exchange vectors LiNa2Al1?2 and LiNaBe1?1, where the former is unique to the Kruta Balka emeralds. Rarely, some Li can also be situated at a channel site, based on stoichiometric considerations. Both Cr- and V-distribution can be very heterogeneous in individual crystals, as shown in the samples from Kruta Balka, Madagascar, and Zimbabwe. Nevertheless, taking average values available for emerald occurrences, the Cr/(Cr+V) ratio (Cr#) in combination with the Mg/(Mg+Fe) ratio (Mg#) and the amount of femag-substitution allows emerald occurrences to be characterized. The "ultramafic" schist-type emeralds with high Cr# and Mg# come from occur-rences where the Fe-Mg-Cr-V component is controlled by the presence of ultramafic meta-igneous rocks. Emeralds with highly variable Mg# come from "sedimentary" localities, where the Fe-Mg-Cr-V component is controlled by metamorphosed sediments such as black shales and carbonates. A "transitional" group has both metasediments and ultramafic rocks as country rocks. Most "ultramafic" schist type occurrences are characterized by a high amount of femag-component, whereas those from the "sedimentary" and "transitional" groups have low femag contents. Growth conditions derived from the zoning pattern combined replacement, sector, and oscillatory zoning in the Kruta Balka emeralds indicate disequilibrium growth from a fluid along with late-stage Na-infiltration. Inclusions in Kruta Balka emeralds (zircon with up to 11 wt% Hf, tourmaline, albite, Sc-bearing apatite) point to a pegmatitic origin.
Abstract: Most natural diamonds are formed in Earth’s lithospheric mantle; however, the exact mechanisms behind their genesis remain debated. Given the occurrence of electrochemical processes in Earth’s mantle and the high electrical conductivity of mantle melts and fluids, we have developed a model whereby localized electric fields play a central role in diamond formation. Here, we experimentally demonstrate a diamond crystallization mechanism that operates under lithospheric mantle pressure-temperature conditions (6.3 and 7.5 gigapascals; 1300° to 1600°C) through the action of an electric potential applied across carbonate or carbonate-silicate melts. In this process, the carbonate-rich melt acts as both the carbon source and the crystallization medium for diamond, which forms in assemblage with mantle minerals near the cathode. Our results clearly demonstrate that electric fields should be considered a key additional factor influencing diamond crystallization, mantle mineral-forming processes, carbon isotope fractionation, and the global carbon cycle.
Abstract: The more than 500 fossil Ca-carbonatite occurrences on Earth are at odds with the only active East African Rift carbonatite volcano, Oldoinyo Lengai (Tanzania), which produces Na-carbonatite magmas. The volcano’s recent major explosive eruptions yielded a mix of nephelinitic and carbonatite melts, supporting the hypothesis that carbonatites and spatially associated peralkaline silicate lavas are related through liquid immiscibility. Nevertheless, previous eruption temperatures of Na-carbonatites were 490–595 °C, which is 250–450 °C lower than for any suitable conjugate silicate liquid. This study demonstrates experimentally that moderately alkaline Ca-carbonatite melts evolve to Na-carbonatites through crystal fractionation. The thermal barrier of the synthetic Na-Ca-carbonate system, held to preclude an evolution from Ca-carbonatites to Na-carbonatites, vanishes in the natural system, where continuous fractionation of calcite + apatite leads to Na-carbonatites, as observed at Oldoinyo Lengai. Furthermore, saturating the Na-carbonatite with minerals present in possible conjugate nephelinites yields a parent carbonatite with total alkali contents of 8–9 wt%, i.e., concentrations that are realistic for immiscible separation from nephelinitic liquids at 1000–1050 °C. Modeling the liquid line of descent along the calcite surface requires a total fractionation of ?48% calcite, ?12% apatite, and ?2 wt% clinopyroxene. SiO2 solubility only increases from 0.2 to 2.9 wt% at 750–1200 °C, leaving little leeway for crystallization of silicates. The experimental results suggest a moderately alkaline parent to the Oldoinyo Lengai carbonatites and therefore a common origin for carbonatites related to alkaline magmatism.
Contributions to Mineralogy and Petrology, doi.org/10.1007/ s00410-020-01708 17p. Pdf
Mantle
carbonatite
Abstract: Carbonatite compositions resulting from melting of magnesian calcite?+?olivine?+?clinopyroxene were experimentally determined in the system CaO-MgO-SiO2-CO2-H2O as a function of temperature and bulk H2O contents at 1.0 and 1.5 GPa. The melting reaction and melt compositions were found to be highly sensitive to H-loss or -gain during experiments. We hence designed a new hydrogen-trap technique, which provided sufficient control to obtain consistent results. The nominally dry solidus temperatures at 1.0 and 1.5 GPa are 1225-1250 °C and 1275-1300 °C, respectively. At 1.0 GPa, the solidus temperature decreases with H2O increasing to 3.5 wt% (1025-1050 °C), then remains approximately constant at higher H2O concentrations. Our nominally dry solidus temperatures are up to 140 °C higher than in previous studies that did not take measures to limit hydrogen infiltration and hence suffered from H2O formation in the capsule. The near-solidus anhydrous melts have 7-8 wt% SiO2 and molar Ca/(Ca?+?Mg) of 0.78-0.82 (XCa). Melting temperatures decrease by as much as 200 °C with increasing XH2O in the coexisting COH-fluid. Concomitantly, near-solidus melt compositions change with increasing bulk H2O from siliceous Ca-rich carbonate melts to Mg-rich silico-carbonatites with up to 27.8 wt% SiO2 and 0.55 XCa. The continuous compositional array of Ca-Mg-Si carbonatites demonstrates the efficient suppression of liquid immiscibility in the alkali-free system. Diopside crystallization was found to be sensitive to temperature and bulk water contents, limiting metasomatic transformation of carbonated upper mantle to wehrlite at 1.0-1.5 GPa to?
Abstract: During the early Archaean, the Earth was too hot to sustain rigid lithospheric plates subject to Wilson Cycle-style plate tectonics. Yet by that time, up to 50% of the present-day continental crust was generated. Preserved continental fragments from the early Archaean have distinct granite-dome/greenstone-keel crust that is interpreted to be the result of a gravitationally unstable stratification of felsic proto-crust overlain by denser mafic volcanic rocks, subject to reorganization by Rayleigh-Taylor flow. Here we provide age constraints on the duration of gravitational overturn in the East Pilbara Terrane. Our U-Pb ages indicate the emplacement of ~3,600-3,460-million-year-old granitoid rocks, and their uplift during an overturn event ceasing about 3,413?million years ago. Exhumation and erosion of this felsic proto-crust accompanied crustal reorganization. Petrology and thermodynamic modelling suggest that the early felsic magmas were derived from the base of thick (~43?km) basaltic proto-crust. Combining our data with regional geochronological studies unveils characteristic growth cycles on the order of 100?million years. We propose that maturation of the early crust over three of these cycles was required before a stable, differentiated continent emerged with sufficient rigidity for plate-like behaviour.
Earth and Planetary Science Letters, Vol. 458, 1, pp.405-417.
Africa, Madagascar
geophysics - seismics
Abstract: The crust and upper mantle of the Madagascar continental fragment remained largely unexplored until a series of recent broadband seismic experiments. An island-wide deployment of broadband seismic instruments has allowed the first study of phase velocity variations, derived from surface waves, across the entire island. Late Cenozoic alkaline intraplate volcanism has occurred in three separate regions of Madagascar (north, central and southwest), with the north and central volcanism active until <1 Ma, but the sources of which remains uncertain. Combined analysis of three complementary surface wave methods (ambient noise, Rayleigh wave cross-correlations, and two-plane-wave) illuminate the upper mantle down to depths of 150 km. The phase-velocity measurements from the three methods for periods of 8-182 s are combined at each node and interpolated to generate the first 3-D shear-velocity model for sub-Madagascar velocity structure. Shallow (upper 10 km) low-shear-velocity regions correlate well with sedimentary basins along the west coast. Upper mantle low-shear-velocity zones that extend to at least 150 km deep underlie the north and central regions of recent alkali magmatism. These anomalies appear distinct at depths <100 km, suggesting that any connection between the zones lies at depths greater than the resolution of surface-wave tomography. An additional low-shear velocity anomaly is also identified at depths 50-150 km beneath the southwest region of intraplate volcanism. We interpret these three low-velocity regions as upwelling asthenosphere beneath the island, producing high-elevation topography and relatively low-volume magmatism.
AGU Advances, doi.org/10.10.1029/2021AV000434, 2p. Pdf
Mantle
diamond inclusions
Abstract: The interior of the Earth at depths greater than about 70 km is entirely devoid of earthquakes, except for a few limited regions associated with current or recent subduction. The absence of earthquakes is expected, since friction along faults becomes too great for brittle failure at these pressures. The difficult question, which has been debated for decades, is what physical process allows deep earthquakes to occur in subduction environments. Now, in a recent publication in AGU Advances, Shirey et al. (2021) provide strong evidence that fluids exist in deep subduction environments, and play a crucial role in producing deep earthquakes.
Earth & Environment Communications, 10.1038/s43247-021-00145-3 16p. Pdf
United States, Hawaii
magmatism
Abstract: Volcanoes represent one of the largest natural sources of metals to the Earth’s surface. Emissions of these metals can have important impacts on the biosphere as pollutants or nutrients. Here we use ground- and drone-based direct measurements to compare the gas and particulate chemistry of the magmatic and lava-seawater interaction (laze) plumes from the 2018 eruption of K?lauea, Hawai’i. We find that the magmatic plume contains abundant volatile metals and metalloids whereas the laze plume is further enriched in copper and seawater components, like chlorine, with volatile metals also elevated above seawater concentrations. Speciation modelling of magmatic gas mixtures highlights the importance of the S2? ligand in highly volatile metal/metalloid degassing at the magmatic vent. In contrast, volatile metal enrichments in the laze plume can be explained by affinity for chloride complexation during late-stage degassing of distal lavas, which is potentially facilitated by the HCl gas formed as seawater boils.
Re-Os dating of sulphide inclusions zonally distributed in single Yakutian diamonds: evidence for multiple episodes of Proterozoic formation and protracted timescales of diamond growth.
Geochimica et Cosmochimica Acta, Vol. 120, pp. 363-394.
Contributions to Mineralogy and Petrology, Vol. 171, pp. 51-
Mantle
Geobarometry
Abstract: The stability of the majorite component in garnet has been experimentally investigated at high pressure and high temperature, focusing on the effect of bulk composition and temperature. High-pressure experiments were performed in a multi-anvil apparatus, at pressures ranging from 6 to 14.5 GPa, and temperatures between 1400 and 1700 °C. Experiments were performed in a range of bulk compositions in the system SiO2-Al2O3-Cr2O3-CaO-MgO with varying Cr/(Cr + Al) ratios. The majorite content of garnet gradually increases with pressure, and the composition of the garnet, specifically the Cr/(Cr + Al) ratio, exerts a significant effect on the majorite substitution. We found no significant effect of temperature. We use the experimental results in combination with the literature data to derive two empirical geobarometers, which can be used to determine the equilibration pressure of natural majoritic garnets of peridotitic and eclogitic bulk compositions. The barometer for peridotitic compositions is
P=?77.1+27.6×Si+1.67×Cr
And the barometer for eclogitic compositions is
P=?29.6+11.8×Si+7.81×Na+4.49×Ca.
Hopp, J., Trieloff, M., Brey, G.P., Woodland, A.B., Simon, N.S.C., Wijbrans, J.R., Siebel, W., Reitter, E.
40 Ar 39 Ar ages of phlogopite in mantle xenoliths from South African kimberlites: evidence for metasomatic mantle impregnation during Kilbaran orogenic cycle.
Abstract: The Kumta and Mercara suture zones welding together Archean crustal blocks in western peninsular India offer critical insights into Precambrian continental juxtapositions and the crustal evolution of eastern Gondwana. Here we present the results from an integrated study of the structure, geology, petrology, mineral chemistry, metamorphic P-T conditions, zircon U-Pb ages and Lu-Hf isotopes of metasedimentary rocks from the two sutures. The dominant rocks in the Kumta suture are greenschist- to amphibolite-facies quartz-phengite schist, garnet-biotite schist, chlorite schist, fuchsite schist and marble. The textural relations, mineral chemistry and thermodynamic modelling of garnet-biotite schist from the Kumta suture indicate peak metamorphic P-T conditions of ca. 11 kbar at 790 °C, with detrital SHRIMP U-Pb zircon ages ranging from 3420 to 2547 Ma, ?Hf (t) values from ? 9.2 to 5.6, and TDMc model ages from 3747 to 2792 Ma. The K-Ar age of phengite from quartz-phengite schist is ca. 1326 Ma and that of biotite from garnet-biotite schist is ca. 1385 Ma, which are interpreted to broadly constrain the timing of metamorphism related to the suturing event. The Mercara suture contains amphibolite- to granulite-facies mylonitic quartzo-feldspathic gneiss, garnet-kyanite-sillimanite gneiss, garnet-biotite-kyanite-gedrite-cordierite gneiss, garnet-biotite-hornblende gneiss, calc-silicate granulite and metagabbro. The textural relations, mineral chemistry and thermodynamic modelling of garnet-biotite-kyanite-gedrite-cordierite gneiss from the Mercara suture indicate peak metamorphic P-T conditions of ca. 13 kbar at 825 °C, followed by isothermal decompression and cooling. For pelitic gneisses from the Mercara suture, LA-ICP-MS U-Pb zircon ages vary from 3249 to 3045 Ma, ?Hf (t) values range from ? 18.9 to 4.2, and TDMc model ages vary from 4094 to 3314 Ma. The lower intercept age of detrital zircons in the pelitic gneisses from the Mercara suture ranges from 1464 to 1106 Ma, indicating the approximate timing of a major lead-loss event, possibly corresponding to metamorphism, and is broadly coeval with events in the Kumta suture. Synthesis of the above results indicates that the Kumta and Mercara suture zones incorporated sediments from Palaeoarchean to Mesoproterozoic sources and underwent high-pressure metamorphism in the late Mesoproterozoic. The protolith sediments were derived from regions containing juvenile Palaeoarchean crust, together with detritus from the recycling of older continental crust. Integration of the above results with published data suggests that the Mesoproterozoic (1460-1100 Ma) Kumta and Mercara suture zones separate the Archean (3400-2500 Ma) Karwar-Coorg block and Dharwar Craton in western peninsular India. Based on regional structural and other geological data we interpret the Kumta and Mercara suture zones as extensions of the Betsimisaraka suture of eastern Madagascar into western India.
Abstract: The Archean Yilgarn Craton in Western Australia hosts at least five generations of Proterozoic mafic dykes, the oldest previously identified dykes belonging to the ca. 2408-2401?Ma Widgiemooltha Supersuite. We report here the first known Archean mafic dyke dated at 2615?±?6?Ma by the ID-TIMS U-Pb method on baddeleyite and at 2610?±?25?Ma using in situ SHRIMP U-Pb dating of baddeleyite. Aeromagnetic data suggest that the dyke is part of a series of NE-trending intrusions that potentially extend hundreds of kilometres in the southwestern part of the craton, here named the Yandinilling dyke swarm. Mafic magmatism at 2615?Ma was possibly related to delamination of the lower crust during the final stages of assembly and cratonisation, and was coeval with the formation of late-stage gold deposit at Boddington. Paleogeographic reconstructions suggest that the Yilgarn and Zimbabwe cratons may have been neighbours from ca. 2690?Ma to 2401?Ma and if the Zimbabwe and Kaapvaal cratons amalgamated at 2660-2610?Ma, the 2615?Ma mafic magmatism in the southwestern Yilgarn Craton may be associated with the same tectonic event that produced the ca. 2607-2604?Ma Stockford dykes in the Central Zone of the Limpopo Belt. Paleomagnetic evidence and a similar tectonothermal evolution, including coeval low-pressure high-temperature metamorphism, voluminous magmatism, and emplacement of mafic dykes, support a configuration where the northern part of the Zimbabwe Craton was adjacent to the western margin of the Yilgarn Craton during the Neoarchean. Worldwide, reliably dated mafic dykes of this age have so far been reported from the Yilgarn Craton, the Limpopo Belt and the São Francisco Craton.
Annual Reviews of Earth and Planetary Sciences, Vol. 47, pp. 173-195.
China
craton
Abstract: The North China Craton (NCC) was originally formed by the amalgamation of the eastern and western blocks along an orogenic belt at ?1.9 Ga. After cratonization, the NCC was essentially stable until the Mesozoic, when intense felsic magmatism and related mineralization, deformation, pull-apart basins, and exhumation of the deep crust widely occurred, indicative of destruction or decratonization. Accompanying this destruction was significant removal of the cratonic keel and lithospheric transformation, whereby the thick (?200 km) and refractory Archean lithosphere mantle was replaced by a thin (<80 km) juvenile one. The decratonization of the NCC was driven by flat slab subduction, followed by a rollback of the paleo-Pacific plate during the late Mesozoic. A global synthesis indicates that cratons are mainly destroyed by oceanic subduction, although mantle plumes might also trigger lithospheric thinning through thermal erosion. Widespread crust-derived felsic magmatism and large-scale ductile deformation can be regarded as petrological and structural indicators of craton destruction.
Lithos, Vol. 406-407. doi: 10.1016/j.lithos.2021.106528 12p. Pdf
Russia
deposit - Azov
Abstract: Zircon megacrysts are commonly found in kimberlites and, together with olivine, low-Cr garnet, pyroxene, phlogopite, and ilmenite megacrysts, they constitute a mineral assemblage known as the "low-Cr suite". The generally close similarity of ages and similar isotope geochemical characteristics of megacrysts and matrix minerals in the host kimberlites support a cognate origin. However, alteration rims commonly develop on zircon and ilmenite megacrysts, providing evidence for a lack of chemical equilibrium between the megacrysts and kimberlitic melts. Here, we report results of a detailed geochronological and geochemical study of zircon megacrysts found in the Middle Devonian Novolaspa kimberlite pipe and dyke located in the Azov Domain of the Ukrainian Shield. The concordia age of zircons is 397.0 ± 2.0 Ma, and it is 14 m.y. older than the age of kimberlite emplacement as defined by a Rb-Sr isochron on phlogopite. The average ?Hf(397) value for unaltered zircon megacrysts is 6.8 ± 0.14, with the alteration rims having similar Hf isotope systematics. These hafnium isotope data indicate a moderately depleted mantle source for zircon. Unaltered megacrystic zircons have low abundances of trace elements and fractionated REE, with pronounced positive Ce/Ce* anomalies and almost no Eu/Eu* anomalies. In contrast, alteration rims have very high and variable concentrations of trace elements, indicating a reaction between zircon and kimberlite melt. The melt or fluid responsible for zircon and ilmenite megacryst formation, in contrast to kimberlitic melt, was poor in incompatible trace elements, except for the HFSE (Zr, Hf, Nb, Ta, and Ti). The oxygen fugacity during crystallization of the megacryst suite was close to the FMQ buffer. Azov zircon megacrysts do not demonstrate close geochronological and isotope-geochemical similarities with their host kimberlites. They are cognate in the broad sense of being related to the same plume event, but their direct affinity is not clearly defined. The megacryst suite may have crystallized from the earliest melts/fluids that separated from the ascending mantle plume, whereas kimberlite magmas were emplaced 14 m.y. after this event.
Abstract: Liquids, glasses, and amorphous materials are ubiquitous in the Earth sciences and are intrinsic to a plethora of geological processes, ranging from volcanic activity, deep Earth melting events, metasomatic processes, frictional melting (pseudotachylites), lighting strikes (fulgurites), impact melting (tektites), hydrothermal activity, aqueous solution geochemistry, and the formation of dense high-pressure structures. However, liquids and glassy materials lack the long-range order that characterizes crystalline materials, and studies of their structure require a different approach to that of conventional crystallography. The pair distribution function is the neutron diffraction technique used to characterize liquid and amorphous states. When combined with atomistic models, neutron diffraction techniques can determine the properties and behavior of disordered structures.
Journal of African Earth Sciences, Vol. 100, pp. 20-41.
Africa, Namibia
Geothermometry
Abstract: Intracontinental deformation accommodated along major lithospheric scale shear zone systems and within associated extensional basins has been well documented within West, Central and East Africa during the Late Cretaceous. The nature of this deformation has been established by studies of the tectonic architecture of sedimentary basins preserved in this part of Africa. In southern Africa, where the post break-up history has been dominated by major erosion, little evidence for post-break-up tectonics has been preserved in the onshore geology. Here we present the results of 38 new apatite fission track analyses from the Damara region of northern Namibia and integrate these new data with our previous results that were focused on specific regions or sections only to comprehensively document the thermo-tectonic history of this region since continental break-up in the Early Cretaceous. The apatite fission track ages range from 449 ± 20 Ma to 59 ± 3 Ma, with mean confined track lengths between 14.61 ± 0.1 ?m (SD 0.95 ?m) to 10.83 ± 0.33 ?m (SD 2.84 ?m). The youngest ages (c. 80–60 Ma) yield the longest mean track lengths, and combined with their spatial distribution, indicate major cooling during the latest Cretaceous. A simple numerical thermal model is used to demonstrate that this cooling is consistent with the combined effects of heating caused by magmatic underplating, related to the Paraná-Etendeka continental flood volcanism associated with rifting and the opening of the South Atlantic, and enhanced erosion caused by major reactivation of major lithospheric structures within southern Africa during a key period of plate kinematic change that occurred in the South Atlantic and SW Indian ocean basins between 87 and 56 Ma. This phase of intraplate tectonism in northern Namibia, focused in discrete structurally defined zones, is coeval with similar phases elsewhere in Africa and suggests some form of trans-continental linkage between these lithospheric zones.
Basin Research, doi.org/10.111 /bre.12527 23p. Pdf
Africa, Namibia
Thermochron, temperature logging
Abstract: Products of onshore passive continental margin erosion are best preserved in offshore sedimentary basins. Therefore, these basins potentially hold a recoverable record of the onshore erosion history. Here, we present apatite fission track (AFT) data for 13 samples from a borehole in the southern Walvis basin, offshore Namibia. All samples show AFT central ages older or similar to their respective stratigraphic ages, while many single grain ages are older, implying none of the samples has been totally annealed post?deposition. Furthermore, large dispersion in single grain ages in some samples suggests multiple age components related to separate source regions. Using Bayesian mixture modelling we classify single grain ages from a given sample to particular age components to create ‘subsamples’ and then jointly invert the entire dataset to obtain a thermal history. For each sample, the post?depositional thermal history is required to be the same for all age components, but each component (‘subsample’) has an independent pre?depositional thermal history. With this approach we can resolve pre? and post?depositional thermal events and identify changes in sediment provenance in response to the syn? and post?rift tectonic evolution of Namibia and southern Africa. Apatite U?Pb and compositional data obtained during the acquisition of LA?ICP?MS FT data are also presented to help track changes in provenance with time. We constrain multiple thermal events linked to the exhumation and burial history of the continental and offshore sectors of the margin over a longer timescale than has been possible using only onshore AFT thermochronological data.
Mineralogy and Petrology, Vol. 115, 19p. Doi.org/101007 /s00710-020- 00723-x pdf
South America, Colombia
REE
Abstract: A multi-methodological study was conducted in order to provide further insight into the structural and compositional complexity of rare earth element (REE) fluorcarbonates, with particular attention to their correct assignment to a mineral species. Polycrystals from La Pita Mine, Municipality de Maripí, Boyacá Department, Colombia, show syntaxic intergrowth of parisite-(Ce) with röntgenite-(Ce) and a phase which is assigned to B3S4 (i.e., bastnäsite-3-synchisite-4; still unnamed) fluorcarbonate. Transmission electron microscope (TEM) images reveal well-ordered stacking patterns of two monoclinic polytypes of parisite-(Ce) as well as heavily disordered layer sequences with varying lattice fringe spacings. The crystal structure refinement from single crystal X-ray diffraction data - impeded by twinning, complex stacking patterns, sequential and compositional faults - indicates that the dominant parisite-(Ce) polytype M1 has space group Cc. Parisite-(Ce), the B3S4 phase and röntgenite-(Ce) show different BSE intensities from high to low. Raman spectroscopic analyses of parisite-(Ce), the B3S4 phase and röntgenite-(Ce) reveal different intensity ratios of the three symmetric CO3 stretching bands at around 1100 cm?1. We propose to non-destructively differentiate parisite-(Ce) and röntgenite-(Ce) by their 1092 cm?1 / 1081 cm?1 ?1(CO3) band height ratio.
Abstract: A multi-methodological study was conducted in order to provide further insight into the structural and compositional complexity of rare earth element (REE) fluorcarbonates, with particular attention to their correct assignment to a mineral species. Polycrystals from La Pita Mine, Municipality de Maripí, Boyacá Department, Colombia, show syntaxic intergrowth of parisite-(Ce) with röntgenite-(Ce) and a phase which is assigned to B3S4 (i.e., bastnäsite-3-synchisite-4; still unnamed) fluorcarbonate. Transmission electron microscope (TEM) images reveal well-ordered stacking patterns of two monoclinic polytypes of parisite-(Ce) as well as heavily disordered layer sequences with varying lattice fringe spacings. The crystal structure refinement from single crystal X-ray diffraction data - impeded by twinning, complex stacking patterns, sequential and compositional faults - indicates that the dominant parisite-(Ce) polytype M1 has space group Cc. Parisite-(Ce), the B3S4 phase and röntgenite-(Ce) show different BSE intensities from high to low. Raman spectroscopic analyses of parisite-(Ce), the B3S4 phase and röntgenite-(Ce) reveal different intensity ratios of the three symmetric CO3 stretching bands at around 1100 cm-1. We propose to non-destructively differentiate parisite-(Ce) and röntgenite-(Ce) by their 1092 cm-1 / 1081 cm-1 ?1(CO3) band height ratio.
Abstract: Subduction zone magmas are more oxidised on eruption than those at mid-ocean ridges. This is attributed either to oxidising components, derived from subducted lithosphere (slab) and added to the mantle wedge, or to oxidation processes occurring during magma ascent via differentiation. Here we provide direct evidence for contributions of oxidising slab agents to melts trapped in the sub-arc mantle. Measurements of sulfur (S) valence state in sub-arc mantle peridotites identify sulfate, both as crystalline anhydrite (CaSO4) and dissolved SO42? in spinel-hosted glass (formerly melt) inclusions. Copper-rich sulfide precipitates in the inclusions and increased Fe3+/?Fe in spinel record a S6+Fe2+ redox coupling during melt percolation through the sub-arc mantle. Sulfate-rich glass inclusions exhibit high U/Th, Pb/Ce, Sr/Nd and ?34S (+?7 to +?11‰), indicating the involvement of dehydration products of serpentinised slab rocks in their parental melt sources. These observations provide a link between liberated slab components and oxidised arc magmas.
Abstract: Clinopyroxene is a key fractionating phase in alkaline magmatic systems, but its impact on metal enrichment processes, and the formation of REE + HFSE mineralisation in particular, is not well understood. To constrain the control of clinopyroxene on REE + HFSE behaviour in sodic (per)alkaline magmas, a series of internally heated pressure vessel experiments was performed to determine clinopyroxene-melt element partitioning systematics. Synthetic tephriphonolite to phonolite compositions were run H2O-saturated at 200?MPa, 650-825?C with oxygen fugacity buffered to log f O2 ? ?QFM + 1 or log f O2 ? ?QFM +5. Clinopyroxene-glass pairs from basanitic to phonolitic fall deposits from Tenerife, Canary Islands, were also measured to complement our experimentally-derived data set. The REE partition coefficients are 0.3-53, typically 2-6, with minima for high-aegirine clinopyroxene. Diopside-rich clinopyroxenes (Aeg5-25) prefer the MREE and have high REE partition coefficients (DEuup to 53, DSmup to 47). As clinopyroxene becomes more Na- and less Ca-rich (Aeg25-50), REE incorporation becomes less favourable, and both the VIM1 and VIIIM2 sites expand (to 0.79 Å and 1.12 Å), increasing DLREE/DMREE. Above Aeg50 both M sites shrink slightly and HREE (VIri? 0.9 Å ? Y) partition strongly onto the VIM1 site, consistent with a reduced charge penalty for REE3+ ? Fe3+ substitution. Our data, complemented with an extensive literature database, constrain an empirical model that predicts trace element partition coefficients between clinopyroxene and silicate melt using only mineral major element compositions, temperature and pressure as input. The model is calibrated for use over a wide compositional range and can be used to interrogate clinopyroxene from a variety of natural systems to determine the trace element concentrations in their source melts, or to forward model the trace element evolution of tholeiitic mafic to evolved peralkaline magmatic systems.
Physics of the Earth and Planetary Interiora, 13p. Pdf
Mantle
melting
Abstract: Physical properties of silicate melts play a key role for global planetary dynamics, controlling for example volcanic eruption styles, mantle convection and elemental cycling in the deep Earth. They are significantly modified by structural changes at the atomic scale due to external parameters such as pressure and temperature or due to chemistry. Structural rearrangements such as 4- to 6-fold coordination change of Si with increasing depth may profoundly influence melt properties, but have so far mostly been studied at ambient temperature due to experimental difficulties. In order to investigate the structural properties of silicate melts and their densification mechanisms at conditions relevant to the deep Earth's interior, we studied haplo basaltic glasses and melts (albite-diopside composition) at high pressure and temperature conditions in resistively and laser-heated diamond anvil cells using X-ray absorption near edge structure spectroscopy. Samples were doped with 10 wt of Ge, which is accessible with this experimental technique and which commonly serves as a structural analogue for the network forming cation Si. We acquired spectra on the Ge K edge up to 48 GPa and 5000 K and derived the average Ge-O coordination number , and bond distance as functions of pressure. Our results demonstrate a continuous transformation from tetrahedral to octahedral coordination between ca. 5 and 30 GPa at ambient temperature. Above 1600 K the data reveal a reduction of the pressure needed to complete conversion to octahedral coordination by ca. 30 . The results allow us to determine the influence of temperature on the Si coordination number changes in natural melts in the Earth's interior. We propose that the complete transition to octahedral coordination in basaltic melts is reached at about 40 GPa, corresponding to a depth of ca. 1200 km in the uppermost lower mantle. At the core-mantle boundary (2900 km, 130 GPa, 3000 K) the existence of non-buoyant melts has been proposed to explain observed low seismic wave velocity features. Our results highlight that the melt composition can affect the melt density at such extreme conditions and may strongly influence the structural response.
Mollex, G., France, L., Furi, E., Bonnet, R., Botcharnikov, R.E., Zimmermann, L., Wilke, S., Deloule, E., Chazot, G., Kazimoto. E.O., Marty, B., Burnard, P.
Abstract: Cognate xenoliths that have been emitted during the last sub-plinian eruption in 2007-08 at Oldoinyo Lengai (OL) represent a unique opportunity to document the igneous processes occuring within the active magma chamber. Detailed petrographic descriptions coupled to a thermobarometric approach, and to the determination of volatile solubility models, allow us to identify the melt evolution at magma chamber conditions, and the storage parameters (P, T). Results indicate that a fresh phonolite melt (~1060°C) was injected into a crustal magma chamber at 11.5 ±3.5 km depth, in agreement with geophysical surveys performed during the eruption. The phonolite contains high volatile contents: 3.2 wt.% H2O and 1.4 wt.% CO2. The liquid line of descent highlights an evolution to nephelinite compositions by cooling down to 880°C. Our results support previous results related to this eruption, and are similar to the historical products emitted during the whole volcano history, allowing us to suggest that no major modification in the plumbing system has occured during the OL evolution. New noble gas results show that: i. fumaroles display constant He isotopic signature since 1988; ii. Cognate xenoliths documenting the active magma chamber and fumaroles display similar He isotopic values (6.58±0.46RA, and 7.31±0.40RA, respectively); iii. OL He isotopic composition is similar to that of other silicate volcanoes of the Arusha region, and comparable to the typical subcontinental lithospheric mantle (SCLM) range (5.2 to 7.0 RA); iv. Ne isotopic ratio of OL is following the MORB signature. Those results are interpreted as showing that 1/ no major modification in the hydrothermal system architecture has occured since 1988 despite major modification of the summit crater morphology, 2/ no contamination by either the atmospheric gases, or crustal material assimilation has occured between the magma chamber and the surface, and 3/ the source of OL and of the other silicate volcanoes in the Arusha region is a SCLM metasomatized by asthenospheric fluids.
Earth & Environment Communications, 10.1038/s43247-021-00145-3 16p. Pdf
United States, Hawaii
magmatism
Abstract: Volcanoes represent one of the largest natural sources of metals to the Earth’s surface. Emissions of these metals can have important impacts on the biosphere as pollutants or nutrients. Here we use ground- and drone-based direct measurements to compare the gas and particulate chemistry of the magmatic and lava-seawater interaction (laze) plumes from the 2018 eruption of K?lauea, Hawai’i. We find that the magmatic plume contains abundant volatile metals and metalloids whereas the laze plume is further enriched in copper and seawater components, like chlorine, with volatile metals also elevated above seawater concentrations. Speciation modelling of magmatic gas mixtures highlights the importance of the S2? ligand in highly volatile metal/metalloid degassing at the magmatic vent. In contrast, volatile metal enrichments in the laze plume can be explained by affinity for chloride complexation during late-stage degassing of distal lavas, which is potentially facilitated by the HCl gas formed as seawater boils.
Mineralogical Magazine Open access special publication Critical metal mineralogy and ore genesis, Vol. 82 (S1) pp. S115-S131.
Europe, Norway
carbonatite
Abstract: The Fen Complex in Norway consists of a ~583 Ma composite carbonatite-ijolite-pyroxenite diatreme intrusion. Locally, high grades (up to 1.6 wt.% total REE) of rare-earth elements (REE) are found in a hydrothermally altered, hematite-rich carbonatite known as rødbergite. The progressive transformation of primary igneous carbonatite to rødbergite was studied here using scanning electron microscopy and inductively coupled plasma-mass spectrometry trace-element analysis of 23 bulk samples taken along a key geological transect. A primary mineral assemblage of calcite, dolomite, apatite, pyrite, magnetite and columbite with accessory quartz, baryte, pyrochlore, fluorite and REE fluorocarbonates was found to have transformed progressively into a secondary assemblage of dolomite, Fe-dolomite, baryte, Ba-bearing phlogopite, hematite with accessory apatite, calcite, monazite-(Ce) and quartz. Textural evidence is presented for REE fluorocarbonates and apatite breaking down in igneous carbonatite, and monazite-(Ce) precipitating in rødbergite. The importance of micro-veins, interpreted as feeder fractures, containing secondary monazite and allanite, is highlighted. Textural evidence for included relics of primary apatite-rich carbonatite are also presented. These acted as a trap for monazite-(Ce) precipitation, a mechanism predicted by physical-chemical experiments. The transformation of carbonatite to rødbergite is accompanied by a 10-fold increase in REE concentrations. The highest light REE (LREE) concentrations are found in transitional vein-rich rødbergite, whereas the highest heavy REE (HREE) and Th concentrations are found within the rødbergites, suggesting partial decoupling of LREE and HREE due to the lower stability of HREE complexes in the aqueous hydrothermal fluid. The hydrothermal fluid involved in the formation of rødbergite was oxidizing and had probably interacted with country-rock gneisses. An ore deposit model for the REE-rich rødbergites is presented here which will better inform exploration strategies in the complex, and has implications for carbonatite-hosted REE resources around the world.
Campbell, L.S., Compston, W., Sircombe, K.N., Wilkinson, C.C.
Zircon from the East orebody of the Bayan Obo Fe Nb REE deposit, China, and SHRIMP ages for carbonatite related magmatism and REE mineralization events.
Contributions to Mineralogy and Petrology, Vol. 168, pp. 1041-
Northern Territories - Coanjula, Daly River-Yambarra, Delamere, DulcieRange, Katherine, Keep River, Mount Bundey, Mount Septimus, Roper River, Victoria
Register of Australian Mining 1991/92, pp. 298-299
Western Australia -Fraser Range, Gladstone, Upper Harris, Joseph BonaparteGulch, Jubilee, Kennedy Bore, King George River, Kununurra, Lake Nabberu, LakeYindarlgooda
Register of Australian Mining 1991/92, pp. 294-295
Western Australia - Leopold Downes-Oscar Range, Leseur Island, MedusaBanks, Liveringa, Mount Alice West, MountBehn, Edith, Elizabeth, McGrath, Noreen, Septimus, Keep, Weld
Upper mantle amphiboles and micas and TiO2, K2O and P2O5 abundances and 100 Mg (Mg+Fe2) ratios of common basalts and andesites: implications for modal mantle metalso
Schmadicke, E., Okrusch, M., Rupprecht-Gutowski, P., Will, T.M.
Garnet pyroxenite, eclogite and alkremite xenoliths from the off-craton Gibeon kimberlite field, Namibia: a window into the upper mantle of the Rehoboth Terrane.
Schmadicke, E., Okrusch, M., Rupprecht-Gutpwski, P., Will, T.M.
Garnet pyroxenite, eclogite and alkremite xenoliths from the off-craton Gibeon kimberlite field, Namibia: a window into the upper mantle of Rehoboth Terrane.
Abstract: Garnets from kimberlite-hosted mantle and a few xenoliths from the lower crust were investigated for water, major, minor, and trace elements. Xenoliths from the mantle comprise pyroxenite, eclogite, alkremite, and peridotite, and crustal xenoliths are mafic high-pressure granulites. Samples from South Africa, Lesotho, and Namibia comprise two principal settings, Kaapvaal Craton (‘on craton’) and Rehoboth terrane (‘off craton’). The composition of garnet depends on rock type but is unrelated to the setting, except for Ti and Cr. In garnets from ‘off craton’ mantle xenoliths, Ti positively correlates with Cr whereas those from ‘on craton’ samples reveal a negative correlation between both elements. Rare earth element patterns indicative of a metasomatic overprint are observed in garnets from both settings, especially in eclogitic garnet. Water contents in garnet are low and range from <1 to about 40 ppm. No setting-related difference occurs, but a weak correlation between water and rock type exists. Water contents in garnets from eclogite and mafic granulite are lower than those in pyroxenite, alkremite, and peridotite. All garnets are water under-saturated, i.e. they do not contain the maximum amount of water that can be accommodated in the mineral structure. Cratonic and non-cratonic samples also show the same characteristics in the infrared (IR) absorption spectra. An absorption band at 3650 cm-1 is typical for most mantle garnets. Bands at 3520 and 3570 cm-1 are present only in TiO2-rich garnets from the Rehoboth terrane and are ascribed to a Ti-related hydrogen substitution. A number of garnets, especially from the Kaapvaal Craton, contain molecular water in addition to structural water. Molecular water is inhomogeneously distributed at grain scale pointing to local interaction with fluid and to disequilibrium at grain scale. These garnets consistently reveal either submicroscopic hydrous phases or additional IR bands at 3630 and 3610-3600 cm-1 caused by structural water. Both features do not occur in garnets in which molecular water is absent. The observations imply (i) relatively late introduction of fluid, at least in cases where hydrous phases formed, and (ii) a relatively dry environment because only water-deficient garnets are able to incorporate additional structural water. Most importantly, they imply (iii) that the low water contents are primary and not due to water loss during upward transport. This late water influx is not responsible for the metasomatic overprint indicated by garnet REE patterns. The results of this study suggest dry conditions in the lithosphere, including mantle and crustal sections of both the Kaapvaal Craton (‘on craton’) and the Rehoboth terrane (‘off craton’). If the low water contents contributed to the stabilization of the Kaapvaal cratonic root (Peslier et al., 2010) the same should apply to the Rehoboth lithosphere where the same variety of rock types occurs. The extremely low water contents in eclogite relative to pyroxenite may be explained by an oceanic crust origin of the eclogites. Subduction and partial melting would cause depletion of water and incompatible elements. The pyroxenites formed by crystal accumulation in the mantle and did not suffer melt depletion. Such a difference in origin can be reconciled with the low Ti contents in eclogitic garnet and the high Ti contents in pyroxenitic garnet.
Abstract: Lenses of ultramafic rocks occur in supracrustal high-grade gneiss in the northern Haskard Highlands, Shackleton Range, East Antarctica. Olivine-bearing garnet pyroxenite is the dominant rock type that is associated with hornblendite and subordinate spinel peridotite and amphibolite. The high-pressure (23-25 kbar) garnet-olivine assemblage of the pyroxenite formed during Pan-African eclogite-facies metamorphism. Associated collisional tectonics led to the incorporation of the ultramafic and mafic rocks in upper crustal rocks of a subducting continental margin. The ultramafic-mafic rocks are tracers of a palaeo-suture zone and are critical for reconstructing Gondwana amalgamation. Thus, it is important to infer the tectonic setting of the rocks prior to emplacement into their current position, i.e. were the rocks part of the oceanic crust, the sub-oceanic, or the sub-continental mantle? Major and trace elements together with Pb and Nd isotope data imply that the precursor rocks of the pyroxenites and hornblendites (the latter being retrogressed pyroxenite equivalents) formed as plume-related melts, with many characteristics typical for ocean-island tholeiitic magmas. Hence, pyroxenite and hornblendite are interpreted as metamorphic equivalents of picritic melts. They differ from most garnet pyroxenites worldwide in composition and genesis. The latter formed as high-pressure clinopyroxene-rich cumulates from basaltic melts. The volumetrically minor amphibolites, sharing many geochemical characteristics with pyroxenites and hornblendites, are also interpreted as metamorphic equivalents of plume-related melts. It is inferred that the picritic melts crystallized at medium- to high-pressure conditions in the upper continental mantle or in the transition zone between mantle and continental crust. The subordinate spinel peridotites are interpreted as fragments of the uppermost, depleted mantle. They are probably the wall rocks into which the picritic melts intruded. The Pb and Nd mantle separation ages of the picritic melts range from 770 to 870 Ma. These model ages are very similar to the emplacement ages of numerous global mafic and ultramafic dykes, which are genetically linked to mantle plume activity that initiated Rodinia rifting and breakup. The protoliths of pyroxenite and related rocks in the Shackleton Range most likely formed during the initial stages of plume magmatism that eventually led to Rodinia breakup.
Abstract: Lenses of ultramafic rocks occur in supracrustal high-grade gneiss in the northern Haskard Highlands, Shackleton Range, East Antarctica. Olivine-bearing garnet pyroxenite is the dominant rock type that is associated with hornblendite and subordinate spinel peridotite and amphibolite. The high-pressure (23-25 kbar) garnet-olivine assemblage of the pyroxenite formed during Pan-African eclogite-facies metamorphism. Associated collisional tectonics led to the incorporation of the ultramafic and mafic rocks in upper crustal rocks of a subducting continental margin. The ultramafic-mafic rocks are tracers of a paleo-suture zone and are critical for reconstructing Gondwana amalgamation. Thus, it is important to infer the tectonic setting of the rocks prior to emplacement into their current position, i.e., were the rocks part of the oceanic crust, the sub-oceanic, or the sub-continental mantle? Major and trace elements together with Pb and Nd isotope data imply that the precursor rocks of the pyroxenites and hornblendites (the latter being retrogressed pyroxenite equivalents) formed as plume-related melts, with many characteristics typical for ocean-island tholeiitic magmas. Hence, pyroxenite and hornblendite are interpreted as metamorphic equivalents of picritic melts. They differ from most garnet pyroxenites worldwide in composition and genesis. The latter formed as high-pressure clinopyroxene-rich cumulates from basaltic melts. The volumetrically minor amphibolites, sharing many geochemical characteristics with pyroxenites and hornblendites, are also interpreted as metamorphic equivalents of plume-related melts. It is inferred that the picritic melts crystallized at medium- to high-pressure conditions in the upper continental mantle or in the transition zone between mantle and continental crust. The subordinate spinel peridotites are interpreted as fragments of the uppermost, depleted mantle. They are probably the wall rocks into which the picritic melts intruded. The Pb and Nd mantle separation ages of the picritic melts range from 770 to 870 Ma. These model ages are very similar to the emplacement ages of numerous global mafic and ultramafic dykes, which are genetically linked to mantle plume activity that initiated Rodinia rifting and breakup. The protoliths of pyroxenite and related rocks in the Shackleton Range most likely formed during the initial stages of plume magmatism that eventually led to the Rodinia breakup.
Abstract: Felsic to intermediate igneous rocks from the Cuchilla Dionisio (or Punta del Este) Terrane (CDT) in Uruguay and the Várzea do Capivarita Complex (VCC) in southern Brazil were emplaced in the Tonian and experienced high-grade metamorphism towards the end of the Cryogenian. Geological and geochemical data indicate an S-type origin and formation in a continental within-plate setting by recycling of lower crustal material that was initially extracted from the mantle in the Palaeoproterozoic. Similar felsic igneous rocks of Tonian age occur in the Richtersveld Igneous Complex and the Vredefontein and Rosh Pinah formations in westernmost South Africa and southern Namibia and have been correlated with their supposed equivalents in Uruguay and Brazil. Geochemical and isotope data of the largely unmetamorphosed felsic igneous rocks in southwestern Africa imply a within-plate origin and formation by partial melting or fractional crystallization of mafic rocks that were extracted from the mantle in the Proterozoic. The parental melts of all of these Tonian igneous rocks from South America and southwestern Africa formed in an anorogenic continental setting at the western margin of the Kalahari Craton and were emplaced in, and/or contaminated by, Namaqua Province-type basement after separation from their source region. However, the source regions and the time of extractions thereof are different and, moreover, occurred at different palaeogeographical latitudes. New petrological data of CDT high-grade gneiss indicate a geothermal gradient of c. 20-25 °C/km, implying continental collisional tectonics following subduction and ocean basin closure at an active continental margin at the eastern edge of present-day South America in the late Cryogenian to early Ediacaran. The associated suture may be traced by the high-grade gneiss and amphibolite-facies mafic rocks in the CDT and probably continues northwards to the Arroio Grande Complex and the VCC in southern Brazil.
Contrasting lower crustal evolution across an Archean Proterozoic suture: physical, chemical and geochronologic studies of lower crustal xenoliths in southern Wyoming and northern Colorado.
American Geophysical Union, Geophysical Monograph, No. 154, pp. 139-162.
Earth and Planteray Science Letters, Vol. 487, pp. 1-17.
Mantle
Core
Abstract: The conventional view of Earth's inner core is that it began to crystallize at Earth's center when the temperature dropped below the melting point of the iron alloy and has grown steadily since that time as the core continued to cool. However, this model neglects the energy barrier to the formation of the first stable crystal nucleus, which is commonly represented in terms of the critical supercooling required to overcome the barrier. Using constraints from experiments, simulations, and theory, we show that spontaneous crystallization in a homogeneous liquid iron alloy at Earth's core pressures requires a critical supercooling of order 1000 K, which is too large to be a plausible mechanism for the origin of Earth's inner core. We consider mechanisms that can lower the nucleation barrier substantially. Each has caveats, yet the inner core exists: this is the nucleation paradox. Heterogeneous nucleation on a solid metallic substrate tends to have a low energy barrier and offers the most straightforward solution to the paradox, but solid metal would probably have to be delivered from the mantle and such events are unlikely to have been common. A delay in nucleation, whether due to a substantial nucleation energy barrier, or late introduction of a low energy substrate, would lead to an initial phase of rapid inner core growth from a supercooled state. Such rapid growth may lead to distinctive crystallization texturing that might be observable seismically. It would also generate a spike in chemical and thermal buoyancy that could affect the geomagnetic field significantly. Solid metal introduced to Earth's center before it reached saturation could also provide a nucleation substrate, if large enough to escape complete dissolution. Inner core growth, in this case, could begin earlier and start more slowly than standard thermal models predict.
Geochimica et Cosmochimica Acta, Vol. 270, pp. 95-111.
China, Russia
metasomatism, melting
Abstract: The eastern part of Asia between the North China and Siberian cratons contains orogenic belts formed by the Paleo-Asian and Pacific subduction and older continental blocks. A fundamental question regarding these and all mobile belts is the fate of the continental lithospheric mantle (CLM) during their formation, i.e. whether, or to what extent the CLM may be formed, replaced or affected during orogeny. Insights into these processes can be obtained from mantle xenoliths hosted by Cenozoic basalts in the Proterozoic Khanka block in the far eastern Russia between NE China and the Pacific coast of Asia. We report petrographic, chemical, and Os-Sr-Nd isotope data for spinel peridotite xenoliths at two Khanka sites: Sviyagin and Podgelban. The modal abundances and chemical compositions suggest that the peridotites are residues of low to moderate degrees of melt extraction from fertile mantle. They show an 187Os/188Os vs. 187Re/188Os correlation with an apparent 1.9?Ga age; the 187Os/188Os ratios are positively correlated with Al2O3 and other melt extraction indices. These results provide the first robust CLM age constraints for the eastern Central Asian Orogenic Belt (CAOB). The ages suggest that the ancient CLM of the Khanka block may be roughly coeval with reworked CLM at Hannuoba (North China craton), and that it persisted through the Phanerozoic orogenies. Moreover, despite the proximity to Phanerozoic subduction zones, the Khanka CLM shows little post-melting enrichment, e.g. the clinopyroxenes are typically LREE-depleted and have Sr-Nd isotope ratios typical of the MORB mantle. We posit that the metasomatism of the CLM, earlier proposed for North China xenolith suites and ascribed to the effects of Pacific or older subduction and related mantle upwelling, may not be widespread in the CAOB. In general, Proterozoic blocks composed of residual peridotites may be more common in the CLM of the SE Siberia and northern China, and possibly other orogenic belts, than previously thought.
Geochimica et Cosmochimica Acta, Vol. 270, pp. 95-111.
Russia
peridotites
Abstract: The eastern part of Asia between the North China and Siberian cratons contains orogenic belts formed by the Paleo-Asian and Pacific subduction and older continental blocks. A fundamental question regarding these and all mobile belts is the fate of the continental lithospheric mantle (CLM) during their formation, i.e. whether, or to what extent the CLM may be formed, replaced or affected during orogeny. Insights into these processes can be obtained from mantle xenoliths hosted by Cenozoic basalts in the Proterozoic Khanka block in the far eastern Russia between NE China and the Pacific coast of Asia. We report petrographic, chemical, and Os-Sr-Nd isotope data for spinel peridotite xenoliths at two Khanka sites: Sviyagin and Podgelban. The modal abundances and chemical compositions suggest that the peridotites are residues of low to moderate degrees of melt extraction from fertile mantle. They show an 187Os/188Os vs. 187Re/188Os correlation with an apparent 1.9?Ga age; the 187Os/188Os ratios are positively correlated with Al2O3 and other melt extraction indices. These results provide the first robust CLM age constraints for the eastern Central Asian Orogenic Belt (CAOB). The ages suggest that the ancient CLM of the Khanka block may be roughly coeval with reworked CLM at Hannuoba (North China craton), and that it persisted through the Phanerozoic orogenies. Moreover, despite the proximity to Phanerozoic subduction zones, the Khanka CLM shows little post-melting enrichment, e.g. the clinopyroxenes are typically LREE-depleted and have Sr-Nd isotope ratios typical of the MORB mantle. We posit that the metasomatism of the CLM, earlier proposed for North China xenolith suites and ascribed to the effects of Pacific or older subduction and related mantle upwelling, may not be widespread in the CAOB. In general, Proterozoic blocks composed of residual peridotites may be more common in the CLM of the SE Siberia and northern China, and possibly other orogenic belts, than previously thought.
Journal of Asian Earth Science, Vol. 200, 104432, 18p. Pdf
India
deposit - Munnar
Abstract: Metacarbonate assemblages in high-grade metamorphic terranes often pose challenges when trying to distinguish between mantle-derived carbonatite and sedimentary carbonate protoliths. We present a study of granulite-facies metacarbonate samples of the putative Munnar carbonatite described as decimeter-thick dikes and veins, and layers of a meter-thick metacarbonate and calc-silicate assemblage, respectively. Thin sections of the metacarbonate dike samples show absence of pyrochlore and ubiquitous scapolite, titanite, wollastonite, and detrital zircons are compatible with impure limestone protoliths. Nd and Sr isotope compositions indicate protoliths with Paleoproterozoic crustal residence times which contrast the mantle sources of Indian and global carbonatites. Trace-element patterns display the characteristics of upper crust, and Ce- and Y-anomalies in a number of samples suggest protolith formation under marine conditions. Carbon and oxygen isotope compositions of the metacarbonate samples interlayered with calc-silicate rocks are similar to those in marine limestone. The metacarbonate dikes, however, show mantle-like compositions which are interpreted as reflecting equilibration with mantle-derived CO2 during granulite-facies metamorphism. The dikes yielded a U-Pb zircon crystallization age of 1020 ± 70 Ma and a cross-cutting quartz syenite, thought to be cogenetic, a magmatic age of 620 ± 35 Ma; the hosting gneiss provided a magmatic age of 2452 ± 14 Ma. We conclude that the layered metacarbonate and calc-silicate rocks represent a former marine limestone and marl sequence and the metacarbonate dikes and veins small-volume melts of crust-derived carbonate-rich sediment.
The dynamic multi-phase eruptive processes and associated deposits of the Argyle ( AK1) lamproite volcanic system, Halls Creek Mobile Zone, Western Australia.
Geological Society of Australia Abstracts, Vol. 90, p. 34. abs.
Examination of diamond stability phase mantle indicator minerals from Leucite Hills, Sweetwater County, Wyoming and Crater of Diamonds State Park, Pike Count, Arkansas.
Geological Society of America, Vol. 48, 3, 1p. Abstract
Abstract: A growing number of studies have suggested that hydrothermal remobilization is crucial for the formation of carbonatite-hosted rare earth element (REE) deposits [1-3]. The Ashram REE deposit, hosted by the Paleoproterozoic Eldor Carbonatite Complex [4], is an example of a REE deposit formed mainly due to hydrothermal processes in magnesio- and ferro-carbonatite. The REE minerals in the Ashram deposit, monazite-(Ce), bastnäsite-(Ce), xenotime- (Y) and minor aeschynite-(Y), are secondary, and were precipitated from hydrothermal fluids. They occur mainly as disseminations, in breccia matrices and veins, and as vug fillings. Hydrothermal apatite and fluorite are also present in appreciable quantities in REE-mineralized zones. Monazite- (Ce) was the earliest REE mineral to form, and was followed by xenotime-(Y) and bastnäsite-(Ce). The compositions of the main REE minerals vary with location in the deposit, particularly in respect to their Nd2O3 and ThO2 contents. Two generations of monazite-(Ce) have been distinguished on the basis of their Nd content. Early, low-Nd monazite-(Ce) formed by replacing apatite through the substitution of 3REE3+ for 5Ca2+ + F- ; low-Nd apatite is LREE-enriched compared to apatite. In contrast, the later high-Nd generation, which has a chondrite-normalized REE profile almost perfectly parallel to that of the apatite, is interpreted to have formed by dissolving the Ca2+ and F- of the apatite and reconstituting the REE and phosphate as monazite-(Ce): Ca4.94REE0.060(PO4)3F = 0.060REEPO4 + F- + 4.94Ca2+ + 2.94PO4 3- Bastnäsite-(Ce) developed as a replacement of monazite- (Ce) through ligand exchange (F- and CO3 2- for PO4 3- ), while preserving the original REE chemistry. A combination of magmatic zone-refinement and hydrothermal remobilization, involving a chloride-bearing fluid, contributed to the formation of a carbonatite-hosted REE deposit.
Abstract: There are a number of peralkaline granitic plutons, which show significant enrichment in the REE and, in some cases, host REE deposits; the grades of the deposits represent the final enrichment in the REE. Thus, it is important to understand how this enrichment occurs and by which processes, in order to develop tools for discovering other similar deposits. The best way to reconstruct the REE composition of an evolving magma is by analysing melt inclusions, i.e., the tiny samples of magma trapped at different stages of its evolution. Such inclusions, however, are rarely preserved and difficult to analyse. Another way to reconstruct the REE composition of an evolving magma is to analyse the REE composition of the minerals crystallising from this magma at different stages in its evolution. This, however, requires that the REE mineral-melt partition coefficients be known. Here we present a model for the calculation of arfvedsonite-melt REE partition coefficients, based on data from the Strange Lake pluton (Canada). The model employs the lattice strain theory, which derives mineral-melt partition coefficients from the values of the ideal partition coefficient (D0), the ideal radius (r0) and the elastic response (EM) of the mineral. There are two sites in arfvedsonite into which the REE partition, namely the M4 site, which is preferred by the light REE and the M2 site, which is preferred by the heavy REE. Partition coefficients for both sites were modelled. Significantly, values of D0, r0 and EM for the M4 site vary linearly with the Ca content of the arfvedsonite, whereas for the M2 site these parameters vary linearly with the temperature of arfvedsonite crystallisation. Using these two relationships, a set of equations was derived, which enables the calculation of arfvedsonite-melt REE partition coefficients for any arfvedsonite for which the Ca content and crystallisation temperature are known. This model was tested on a peralkaline granitic pegmatite from the Amis complex (Namibia), for which data on the composition of the amphibole and corresponding magma (melt inclusions) have been reported. The model successfully predicts the concentrations of the various REE in the Amis magma, thereby providing confidence that it can be used to trace the REE content of evolving granitic magmas in other plutons.
Flourine , yttrium and lanthaide rich cerianite (Ce) from carbonatitic rocks of the Kerimasi volcano and surrounding explosive craters Gregory Rift Tanzania.
Mineralogical Magazine, Vol. 75, 6, pp. 2813-2822.
The Genesis of the Diamond. a Geological, Mineralogical, Crystallographical, Petrographical and Chemical Study of Kimberlite and its Associated Cognate and Accidental Inclusions.
Critical evaluation of the status of the areas for future research regarding the wide band GAP semi-conductors diamond, gallium nitride and silicon carbide
Material Sci. Eng. B. Solid State Adv. Technol, Vol. B1, No. 1, Aug. pp. 77-104
Abstract: Geochemical variations in volcanic rocks erupted at Earth's surface indicate differences in mantle composition, but our understanding of the location, formation, and history of compositionally distinct mantle domains remains incomplete. In particular, some hotspot lavas contain signatures of primitive regions within the mantle that have remained relatively isolated and unprocessed throughout Earth's history. Here we use models of mantle flow to predict the locations within the mantle that are sampled by the mantle plumes associated with hotspot volcanism. Combining these models of mantle flow with state?of?the?art seismic images and a comprehensive catalog of hotspot lava geochemistry, we find that hotspots with a more primitive geochemical signature (as indicated by the isotopes of helium) sample the two large low shear?velocity provinces in the lowermost mantle. Complementary constraints from xenon and tungsten isotope ratios associated with primitive materials then require these continent?sized provinces in Earth's deep interior formed early in Earth's history, survived the violent Moon?forming giant impact, and remained relatively unmixed with the rest of the solid Earth over the past 4.5 billion years.
Geochemistry, Geophysics, Geosystems, Vol. 20, 8, pp. 4130-4145.
Mantle
geophysics - seismics
Abstract: Geochemical variations in volcanic rocks erupted at Earth's surface indicate differences in mantle composition, but our understanding of the location, formation, and history of compositionally distinct mantle domains remains incomplete. In particular, some hotspot lavas contain signatures of primitive regions within the mantle that have remained relatively isolated and unprocessed throughout Earth's history. Here we use models of mantle flow to predict the locations within the mantle that are sampled by the mantle plumes associated with hotspot volcanism. Combining these models of mantle flow with state-of-the-art seismic images and a comprehensive catalog of hotspot lava geochemistry, we find that hotspots with a more primitive geochemical signature (as indicated by the isotopes of helium) sample the two large low shear-velocity provinces in the lowermost mantle. Complementary constraints from xenon and tungsten isotope ratios associated with primitive materials then require these continent-sized provinces in Earth's deep interior formed early in Earth's history, survived the violent Moon-forming giant impact, and remained relatively unmixed with the rest of the solid Earth over the past 4.5 billion years.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Rare earth elements in phoscorites and carbonatites of the Devonian Kola alkaline province, Russia: examples from Kovdor, Khibina, Vuoriyarvi and Turiy Mys complexes.
Abstract: The Zambezi rises with considerable modesty in north-west Zambia from a small spring on the gentle upland of the Southern Equatorial Divide - the watershed that separates the river from north-west-flowing tributaries of the Congo. The evolution of the Zambezi River has repeatedly modified the distribution of riverine plant and animal species. The hydrology of the Zambezi is further influenced by water exploitation by different users, along its main channel and tributaries. The dams have had severe ecological impacts on the major floodplains, as a result of the reduction of the supply of water and sediment. The major Early Cretaceous Zambezi-Limpopo River system entered the Mozambique coastal plain via a line of crustal weakness that was exploited by a major west-north-west trending dyke swarm. Drainage evolution of the Palaeo-Chambeshi system has been invoked as the primary cause of the recent evolution of the molerats.
Geochimica et Cosmochimica Acta, Vol. 238, pp. 542-562.
Canada, Nunavut, Baffin Island
picrites
Abstract: Young (61?Ma) unaltered picrites from Baffin Island, northeast Canada, possess some of the highest 3He/4He (up to 50?Ra) seen on Earth, and provide a unique opportunity to study primordial mantle that has escaped subsequent chemical modification. These high-degree partial melts also record anomalously high 182W/184W ratios, but their Sr-Nd-Hf-Pb isotopic compositions (including 142Nd) are indistinguishable from those of North Atlantic mid-ocean ridge basalts. New high precision Fe and Zn stable isotope analyses of Baffin Island picrites show limited variability with ?56Fe ranging from ?0.03‰ to 0.13‰ and ?66Zn varying from 0.18‰ to 0.28‰. However, a clear inflection is seen in both sets of isotope data around the composition of the parental melt (MgO?=?21?wt%; ?56Fe?=?0.08?±?0.04‰; and ?66Zn?=?0.24?±?0.03‰), with two diverging trends interpreted to reflect the crystallisation of olivine and spinel in low-MgO samples and the accumulation of olivine at higher MgO. Olivine mineral separates are significantly isotopically lighter than their corresponding whole rocks (?56Fe????0.62‰ and ?66Zn????0.22‰), with analyses of individual olivine phenocrysts having extremely variable Fe isotope compositions (?56Fe?=??0.01‰ to ?0.80‰). By carrying out modelling in three-isotope space, we show that the very negative Fe isotope compositions of olivine phenocryst are the result of kinetic isotope fractionation from disequilibrium diffusional processes. An excellent correlation is observed between ?56Fe and ?66Zn, demonstrating that Zn isotopes are fractionated by the same processes as Fe in simple systems dominated by magmatic olivine. The incompatible behaviour of Cu during magmatic evolution is consistent with the sulfide-undersaturated nature of these melts. Consequently Zn behaves as a purely lithophile element, and estimates of the bulk Earth Zn isotope composition based on Baffin Island should therefore be robust. The ancient undegassed lower mantle sampled at Baffin Island possesses a ?56Fe value that is within error of previous estimates of bulk mantle ?56Fe, however, our estimate of the Baffin mantle ?66Zn (0.20?±?0.03‰) is significantly lower than some previous estimates. Comparison of our new data with those for Archean and Proterozoic komatiites is consistent with the Fe and Zn isotope composition of the mantle remaining constant from at least 3?Ga to the present day. By focusing on large-degree partial melts (e.g. komatiites and picrites) we are potenitally biasing our record to samples that will inevitably have interacted with, entrained and melted the ambient shallow mantle during ascent. For a major element such as Fe, that will continuosly participate in melting as it rises through the mantle, the final isotopic compositon of the magama will be a weighted average of the complete melting column. Thus it is unsuprising that minimal Fe isotope variations are seen between localities. In contrast, the unique geochemical signatures (e.g. He and W) displayed by the Baffin Island picrites are inferred to solely originate from the lowermost mantle and will be continuously diluted upon magma ascent.
Abstract: Estimates of the volume of the earliest crust based on zircon ages and radiogenic isotopes remain equivocal. Stable isotope systems, such as molybdenum, have the potential to provide further constraints but remain underused due to the lack of complementarity between mantle and crustal reservoirs. Here we present molybdenum isotope data for Archaean komatiites and Phanerozoic komatiites and picrites and demonstrate that their mantle sources all possess subchondritic signatures complementary to the superchondritic continental crust. These results confirm that the present-day degree of mantle depletion was achieved by 3.5 billion years ago and that Earth has been in a steady state with respect to molybdenum recycling. Mass balance modelling shows that this early mantle depletion requires the extraction of a far greater volume of mafic-dominated protocrust than previously thought, more than twice the volume of the continental crust today, implying rapid crustal growth and destruction in the first billion years of Earth’s history.
Proceedings National Academy of Science, Vol. 116, pp. 407-412.
Australia
paleomagnetism
Abstract: Zircon crystals from the Jack Hills, Western Australia, are one of the few surviving mineralogical records of Earth’s first 500 million years and have been proposed to contain a paleomagnetic record of the Hadean geodynamo. A prerequisite for the preservation of Hadean magnetization is the presence of primary magnetic inclusions within pristine igneous zircon. To date no images of the magnetic recorders within ancient zircon have been presented. Here we use high-resolution transmission electron microscopy to demonstrate that all observed inclusions are secondary features formed via two distinct mechanisms. Magnetite is produced via a pipe-diffusion mechanism whereby iron diffuses into radiation-damaged zircon along the cores of dislocations and is precipitated inside nanopores and also during low-temperature recrystallization of radiation-damaged zircon in the presence of an aqueous fluid. Although these magnetites can be recognized as secondary using transmission electron microscopy, they otherwise occur in regions that are indistinguishable from pristine igneous zircon and carry remanent magnetization that postdates the crystallization age by at least several hundred million years. Without microscopic evidence ruling out secondary magnetite, the paleomagnetic case for a Hadean-Eoarchean geodynamo cannot yet been made.
Abstract: The differentiation of Earth ~4.5 billion years (Ga) ago is believed to have culminated in magma ocean crystallization, crystal-liquid separation, and the formation of mineralogically distinct mantle reservoirs. However, the magma ocean model remains difficult to validate because of the scarcity of geochemical tracers of lower mantle mineralogy. The Fe isotope compositions (?57Fe) of ancient mafic rocks can be used to reconstruct the mineralogy of their mantle source regions. We present Fe isotope data for 3.7-Ga metabasalts from the Isua Supracrustal Belt (Greenland). The ?57Fe signatures of these samples extend to values elevated relative to modern equivalents and define strong correlations with fluid-immobile trace elements and tungsten isotope anomalies (?182W). Phase equilibria models demonstrate that these features can be explained by melting of a magma ocean cumulate component in the upper mantle. Similar processes may operate today, as evidenced by the ?57Fe and ?182W heterogeneity of modern oceanic basalts.
Geological studies in the Wabigoon, Quetico and Abitibi Wawa subprovinces Superior Province of Ontario, with emphasis on the struct. dev.Beardmore-Geraldton.belt
Ontario Geological Survey Open File, No. 5724, 189p
Subprovince accretion in the southern Superior Province or cross section through the Wawa-Quetico-Wabigoon subprovincial boundaries and Beardmore-Geraldtonbelt
Geological Association of Canada (GAC) Annual Meeting held Toronto May 1991, Guidebook, No. B6, 25p
Granite-greenstone terranes in the Pilbara Block,Australia, as coeval volcano plutonic complexes; evidence from uranium-lead (U-Pb) (U-Pb) zircon dating of the Mt. EdgarBatholith
Earth and Planetary Science Letters, Vol. 97, No. 1-2, February pp. 41-53
Carboniferous and Triassic eclogites in the Western Dabie Mountains east central Chin a: evidence for protracted convergence of the North and South Chin a Blocks.
Journal of Metamorphic Geology, Vol. 20, 9, pp. 873-886.
Lower crustal xenoliths from Jurassic kimberlite diatremes, Upper Michigan USA: evidence for Proterozoic orogenesis and plume magmatism in the lower crust of the southern Superior Province.
Abstract: The Bayan Obo ore deposit in Inner Mongolia, North China, the largest-known rare earth element (REE) deposit in the world, is closely associated with carbonatite dykes. Scarce zircon grains, with a wide range of ages and diverse origins, have been extracted from the Wu dyke, a REE-enriched calcitic carbonatite dyke 2?km from the East Ore Body of the Bayan Obo deposit. Three zircon populations were identified based on ages and trace element compositions: 1) Captured zircons with Paleoproterozoic and Archean ages. These zircons have REE patterns and moderate Th/U ratios similar to zircon with silicate inclusions from basement igneous rocks, which have been recognized as contaminants from wall rocks. 2) Carbonatite magmatic zircons with Mesoproterozoic ages. These zircons have high to extremely high Th/U ratios (13-1600), a characteristic signature of the Bayan Obo deposit. Two zircon grains yielded concordant 206Pb/238U ages (1.27?±?0.11?Ga???1.42?±?0.18?Ga) and 208Pb/232Th age (1.26?±?0.20?Ga) with calcite inclusions, indicating that the Wu dyke was emplaced at ca. 1.34?Ga, which coincides with a worldwide generation of Mesoproterozoic kimberlites, lamprophyres, carbonatites, and anorogenic magmatism. 3) Hydrothermal zircons with Caledonian and Triassic ages. The Caledonian zircon has 206Pb/238U age of 381?±?4?Ma and 208Pb/232Th age of 367?±?14?Ma with dolomite inclusion. These evidences are consistent with multiple stages of mineralization, Mesoproterozoic calcite carbonatite magmatism interacted by protracted fluxing of subduction-released Caledonian fluids during the closure of the Palaeo-Asian Ocean, coupled with interaction with the mantle wedge and metasomatism of overlying sedimentary carbonate.
Abstract: The Bayan Obo ore deposit in Inner Mongolia, North China, the largest-known rare earth element (REE) deposit in the world, is closely associated with carbonatite dykes. Scarce zircon grains, with a wide range of ages and diverse origins, have been extracted from the Wu dyke, a REE-enriched calcitic carbonatite dyke 2?km from the East Ore Body of the Bayan Obo deposit. Three zircon populations were identified based on ages and trace element compositions: 1) Captured zircons with Paleoproterozoic and Archean ages. These zircons have REE patterns and moderate Th/U ratios similar to zircon with silicate inclusions from basement igneous rocks, which have been recognized as contaminants from wall rocks. 2) Carbonatite magmatic zircons with Mesoproterozoic ages. These zircons have high to extremely high Th/U ratios (13-1600), a characteristic signature of the Bayan Obo deposit. Two zircon grains yielded concordant 206Pb/238U ages (1.27?±?0.11?Ga???1.42?±?0.18?Ga) and 208Pb/232Th age (1.26?±?0.20?Ga) with calcite inclusions, indicating that the Wu dyke was emplaced at ca. 1.34?Ga, which coincides with a worldwide generation of Mesoproterozoic kimberlites, lamprophyres, carbonatites, and anorogenic magmatism. 3) Hydrothermal zircons with Caledonian and Triassic ages. The Caledonian zircon has 206Pb/238U age of 381?±?4?Ma and 208Pb/232Th age of 367?±?14?Ma with dolomite inclusion. These evidences are consistent with multiple stages of mineralization, Mesoproterozoic calcite carbonatite magmatism interacted by protracted fluxing of subduction-released Caledonian fluids during the closure of the Palaeo-Asian Ocean, coupled with interaction with the mantle wedge and metasomatism of overlying sedimentary carbonate.
Laser ablation inductively coupled plasma mass spectrometry(LA-ICP-MS):rapid technique direct quantitative determination major, trace rareearth elements
Abstract: A large compilation of quality-curated major and trace element data has been assembled to investigate how trace element patterns of mafic and ultramafic magmas have varied with time through particular settings from the Archean to the Phanerozoic, the primary objective being to recognise at what times particular patterns of variation emerge, and how similar these are to baseline data sets representing tectonic settings in the modern Earth. The most informative element combinations involve Nb, Th and the REE, where REE are represented by ‘lambda’ parameters describing slope and shape of patterns. Combinations of the ratios of Th, Nb, La and lambda values from Archean and early Proterozoic basalts and komatiites reveal a distinctive pattern that is common in most well-sampled terranes, defining a roughly linear trend in multi-dimensional space from compositions intermediate between modern n-MORB and primitive mantle at one end, towards compositions approximating middle-to-upper continental crust at the other. We ascribe this ‘Variable Th/Nb’ trend in most instances to varying degrees of crustal contamination of magmas with similar compositions to modern oceanic plateau basalts. Komatiites had slightly more depleted sources than basalts, consistent with the hypothesis of derivation from plume tails and heads, respectively. The most significant difference between Precambrian and Phanerozoic plume-derived basalts is that the distinctive OIB-like enriched source component appears to be largely missing from the Archean and Proterozoic geologic record, although isolated examples of OIB-like trace element characteristics are evident in datasets from even the oldest preserved greenstones. Phanerozoic intra-cratonic LIPs, such as the 260?Ma Emeishan LIP in China, have fundamentally different geochemical characteristics to Archean and Paleoproterozoic assemblages; the oldest Proterozoic LIP we have identified that has this type of ‘modern’ signal is the Midcontinent Rift at 1100?Ma. The data are consistent with plume tail sources having changed from being dominantly depleted in the Archean Earth to dominantly enriched in the Phanerozoic Earth, while plume head sources have hardly changed at all. Trace element patterns considered to be diagnostic of subduction are locally present but rare in Archean terranes and become more prevalent through the Proterozoic, although this conclusion is tempered by the large degree of overlap in compositional space between continental arc magmas and continental flood basalts. This overlap reflects the difficulty of distinguishing the effects of supra-subduction metasomatizm and flux melting from those of crustal contamination. Additional factors must also be borne in mind, particularly that trace element partitioning systematics may have been different in all environments in a hotter planet, and large-scale asthenospheric overturns might have been predominant over modern-style plumes in the Archean Earth. Some basaltic suites in particular Archean terranes, notably the western parts of both the Yilgarn and Pilbara cratons in Western Australia and parts of the Superior Craton, have restricted, but locally predominant, suites of basalts with characteristics akin to modern oceanic arcs, suggesting that some process similar to modern subduction was preserved in these particular belts. Ferropicrite magmas with distinctive characteristics typical of modern OIBs and some continental LIPs (notably Emeishan) are rare but locally predominant in some Archean and early Proterozoic terranes, implying that plume sources were beginning to be fertilised by enriched, probably subducted, components as far back as the Mesoarchean. We see no evidence for discontinuous secular changes in mantle-derived magmatism with time that could be ascribed to major mantle reorganisation events. The Archean-Proterozoic transition appears to be entirely gradational from this standpoint. The transition from Archean-style to Phanerozoic-style plume magmatism took place somewhere between 1900?Ma (age of the Circum-Superior komatiitic basalt suites) and 1100?Ma (the age of the Midcontinent Rift LIP).
U Pb Hf isotopic analysis of zircon in lower crustal xenoliths from the Navajo volcanic field: 1.4 Ga mafic magmatism and metamorphism beneath Colorado Plateau.
Contributions to Mineralogy and Petrology, Vol. 151, 3, pp. 313-330.
Multistage exhumation and juxaposition of lower continental crust in the western Canadian Shield: linking high resolution U Pb and 40 Ar / 39 Ar thermochronometry with pressure temperature deformation paths.
Abstract: Large peridotite massifs are scattered along the 1500?km length of the Yarlung-Zangbo Suture Zone (southern Tibet, China), the major suture between Asia and Greater India. Diamonds occur in the peridotites and chromitites of several massifs, together with an extensive suite of trace phases that indicate extremely low fO2 (SiC, nitrides, carbides, native elements) and/or ultrahigh pressures (UHP) (diamond, TiO2 II, coesite, possible stishovite). New physical and isotopic (C, N) studies of the diamonds indicate that they are natural, crystallized in a disequilibrium, high-T environment, and spent only a short time at mantle temperatures before exhumation and cooling. These constraints are difficult to reconcile with previous models for the history of the diamond-bearing rocks. Possible evidence for metamorphism in or near the upper part of the Transition Zone includes the following: (1) chromite (in disseminated, nodular and massive chromitites) containing exsolved pyroxenes and coesite, suggesting inversion from a high-P polymorph of chromite; (2) microstructural studies suggesting that the chromitites recrystallized from fine-grained, highly deformed mixtures of wadsleyite and an octahedral polymorph of chromite; (3) a new cubic Mg-silicate, with the space group of ringwoodite but an inverse-spinel structure (all Si in octahedral coordination); (4) harzburgites with coarsely vermicular symplectites of opx + Cr-Al spinel ± cpx; reconstructions suggest that these are the breakdown products of majoritic garnets, with estimated minimum pressures to?>?13?GPa. Evidence for a shallow pre-metamorphic origin for the chromitites and peridotites includes the following: (1) trace-element data showing that the chromitites are typical of suprasubduction-zone (SSZ) chromitites formed by magma mixing or mingling, consistent with Hf-isotope data from magmatic (375?Ma) zircons in the chromitites; (2) the composition of the new cubic Mg-silicate, which suggests a low-P origin as antigorite, subsequently dehydrated; (3) the peridotites themselves, which carry the trace element signature of metasomatism in an SSZ environment, a signature that must have been imposed before the incorporation of the UHP and low-fO2 phases. A proposed P-T-t path involves the original formation of chromitites in mantle-wedge harzburgites, subduction of these harzburgites at c. 375?Ma, residence in the upper Transition Zone for >200 Myr, and rapid exhumation at c. 170-150?Ma or 130-120?Ma. Os-isotope data suggest that the subducted mantle consisted of previously depleted subcontinental lithosphere, dragged down by a subducting oceanic slab. Thermomechanical modeling shows that roll-back of a (much later) subducting slab would produce a high-velocity channelized upwelling that could exhume the buoyant harzburgites (and their chromitites) from the Transition Zone in?
Eocene shoshonitic mafic dykes intruding the Monashee Complex, British Columbia: a petrogenetic relationship with the Kam loops Group volcanic sequence.
Canadian Journal of Earth Sciences, Vol. 42, 1, pp. 11-24.
Metamorphosed boninitic basalts, arc tholeiites, and cryptic volcanics tratigraphy from the Elzevir Terrane of the Grenville Province, Calumet mine, Quebec
Canadian Journal of Earth Sciences, Vol. 29, No. 1, January pp. 26-34
Majoritic garnet: a new approach to pressure estimation of shock events in meteorites and the encapsulation of sub-lithospheric inclusions in diamonds.
Geochimica et Cosmochimica Acta, Vol. 74, 20, pp. 5939-5937.
Geophysical Research Letters, Vol. 43, 8, pp. 3693-3697.
Mantle
Melting
Abstract: Seismic tomography models reveal two large low shear velocity provinces (LLSVPs) that identify large-scale variations in temperature and composition in the deep mantle. Other characteristics include elevated density, elevated bulk sound speed, and sharp boundaries. We show that properties of LLSVPs can be explained by the presence of small quantities (0.3-3%) of suspended, dense Fe-Ni-S liquid. Trapping of metallic liquid is demonstrated to be likely during the crystallization of a dense basal magma ocean, and retention of such melts is consistent with currently available experimental constraints. Calculated seismic velocities and densities of lower mantle material containing low-abundance metallic liquids match the observed LLSVP properties. Small quantities of metallic liquids trapped at depth provide a natural explanation for primitive noble gas signatures in plume-related magmas. Our model hence provides a mechanism for generating large-scale chemical heterogeneities in Earth's early history and makes clear predictions for future tests of our hypothesis.
Geophysical Research Letters, Vol. 43, 8, pp. 3693-3699.
Mantle
Melting
Abstract: Seismic tomography models reveal two large low shear velocity provinces (LLSVPs) that identify large-scale variations in temperature and composition in the deep mantle. Other characteristics include elevated density, elevated bulk sound speed, and sharp boundaries. We show that properties of LLSVPs can be explained by the presence of small quantities (0.3 -3%) of suspended, dense Fe-Ni-S liquid. Trapping of metallic liquid is demonstrated to be likely during the crystallization of a dense basal magma ocean, and retention of such melts is consistent with currently available experimental constraints. Calculated seismic velocities and densities of lower mantle material containing low-abundance metallic liquids match the observed LLSVP properties. Small quantities of metallic liquids trapped at depth provide a natural explanation for primitive noble gas signatures in plume-related magmas. Our model hence provides a mechanism for generating large-scale chemical heterogeneities in Earth's early history and makes clear predictions for future tests of our hypothesis.
Annual Review of Earth and Planetary Sciences, Vol. 46, pp. 47-66.
Mantle
geothermometry
Abstract:
The thermal conductivity of iron alloys at high pressures and temperatures is a critical parameter in governing (a) the present-day heat flow out of Earth's core, (b) the inferred age of Earth's inner core, and (c) the thermal evolution of Earth's core and lowermost mantle. It is, however, one of the least well-constrained important geophysical parameters, with current estimates for end-member iron under core-mantle boundary conditions varying by about a factor of 6. Here, the current state of calculations, measurements, and inferences that constrain thermal conductivity at core conditions are reviewed. The applicability of the Wiedemann-Franz law, commonly used to convert electrical resistivity data to thermal conductivity data, is probed: Here, whether the constant of proportionality, the Lorenz number, is constant at extreme conditions is of vital importance. Electron-electron inelastic scattering and increases in Fermi-liquid-like behavior may cause uncertainties in thermal conductivities derived from both first-principles-associated calculations and electrical conductivity measurements. Additional uncertainties include the role of alloying constituents and local magnetic moments of iron in modulating the thermal conductivity. Thus, uncertainties in thermal conductivity remain pervasive, and hence a broad range of core heat flows and inner core ages appear to remain plausible.
Abstract: Bastnäsite-(Ce), a rare earth element (REE) bearing carbonate (Ce,La,Y,Nd,Pr)CO3F, is one of the most common REE-bearing minerals and has importance from both economic and geologic perspectives due to its large REE concentration. It also provides an example of the structural interplay between carbonate groups and fluorine ions, as well as the complex bonding properties of rare earth elements. We report Raman vibrational and Nd3+ luminescence (4F3/2?4I9/2, 4F3/2?4I11/2, and 4F5/2+2H9/2?4I9/2) spectra of natural bastnäsite-(Ce) to 50 GPa at 300 K. Two phase transitions are observed under compression. Bastnäsite-I remains the stable phase up to 25 GPa, where it undergoes a subtle phase transition to bastnäsite-II. This is likely produced by a change in symmetry of the carbonate ion. Bastnäsite-II transforms to bastnäsite-III at ~38 GPa, as demonstrated by changes in the luminescence spectra. This second transition is particularly evident within the 4F3/2?4I9/2 luminescent transitions, and it appears that a new rare earth element site is generated at this phase change. This transition is also accompanied by modest changes in both the Raman spectra and two sets of luminescent transitions. Despite these transformations, the carbonate unit remains a stable, threefold-coordinated unit throughout this pressure range, with a possible increase in its distortion. Correspondingly, the rare-earth element site(s) appears to persist in quasi-ninefold coordination as well, implying that the general bonding configuration in bastnäsite is at least metastable over a ~30% compression range. All pressure-induced transitions are reversible, with some hysteresis, reverting to its ambient pressure phase on decompression.
Geological Society of America Bulletin, Vol. 133, 3/4, pp. 625-646. pdf
Global
Pangea
Abstract: The supercontinent Pangea formed by the subduction of the Iapetus and Rheic oceans between Gondwana, Laurentia, and Baltica during mid-to-late Paleozoic times. However, there remains much debate regarding how this amalgamation was achieved. Most paleogeographic models based on paleomagnetic data argue that the juxtaposition of Gondwana and Laurussia (Laurentia-Baltica) was achieved via long-lasting highly oblique convergence in the late Paleozoic. In contrast, many geology-based reconstructions suggest that the collision between the two continents was likely initiated via a Gondwanan promontory comprising the Iberian, Armorican, and Bohemian massifs, and parts of the basement units in the Alpine orogen during the Early Devonian. To help resolve this discrepancy, we present an updated compilation of high-quality paleopoles of mid-to-late Paleozoic ages (spanning Middle Ordovician and Carboniferous times) from Gondwana, Laurentia, and Baltica. These paleopoles were evaluated with the Van der Voo selection criteria, corrected for inclination error where necessary, and were used to revise their apparent polar wander (APW) paths. The revised APW paths were constructed using an innovative approach in which age errors, A95 ovals, and Q-factors of individual paleopoles are taken into account. By combining the resulting APW paths with existing geological data and field relationships in the European Variscides, we provide mid-to-late Paleozoic paleogeographic reconstructions which indicate that the formation of Pangea was likely initiated at 400 Ma via the collision between Laurussia and a ribbon-like Gondwanan promontory that was itself formed by a scissor-like opening of the Paleotethys Ocean, and that the amalgamation culminated in the mostly orthogonal convergence between Gondwana and Laurussia.
An open source software environment for visualizing and refining plate tectonic reconstructions using high resolution geological and geophysical dat a sets.
Abstract: Rifted margins are formed by persistent stretching of continental lithosphere until breakup is achieved. It is well known that strain-rate-dependent processes control rift evolution1, 2, yet quantified extension histories of Earth’s major passive margins have become available only recently. Here we investigate rift kinematics globally by applying a new geotectonic analysis technique to revised global plate reconstructions. We find that rifted margins feature an initial, slow rift phase (less than ten millimetres per year, full rate) and that an abrupt increase of plate divergence introduces a fast rift phase. Plate acceleration takes place before continental rupture and considerable margin area is created during each phase. We reproduce the rapid transition from slow to fast extension using analytical and numerical modelling with constant force boundary conditions. The extension models suggest that the two-phase velocity behaviour is caused by a rift-intrinsic strength-velocity feedback, which can be robustly inferred for diverse lithosphere configurations and rheologies. Our results explain differences between proximal and distal margin areas3 and demonstrate that abrupt plate acceleration during continental rifting is controlled by the nonlinear decay of the resistive rift strength force. This mechanism provides an explanation for several previously unexplained rapid absolute plate motion changes, offering new insights into the balance of plate driving forces through time.
Abstract: Volcanic hotspot tracks featuring linear progressions in the age of volcanism are typical surface expressions of plate tectonic movement on top of narrow plumes of hot material within Earth’s mantle1. Seismic imaging reveals that these plumes can be of deep origin2=probably rooted on thermochemical structures in the lower mantle3, 4, 5, 6. Although palaeomagnetic and radiometric age data suggest that mantle flow can advect plume conduits laterally7, 8, the flow dynamics underlying the formation of the sharp bend occurring only in the Hawaiian-Emperor hotspot track in the Pacific Ocean remains enigmatic. Here we present palaeogeographically constrained numerical models of thermochemical convection and demonstrate that flow in the deep lower mantle under the north Pacific was anomalously vigorous between 100 million years ago and 50 million years ago as a consequence of long-lasting subduction systems, unlike those in the south Pacific. These models show a sharp bend in the Hawaiian-Emperor hotspot track arising from the interplay of plume tilt and the lateral advection of plume sources. The different trajectories of the Hawaiian and Louisville hotspot tracks arise from asymmetric deformation of thermochemical structures under the Pacific between 100 million years ago and 50 million years ago. This asymmetric deformation waned just before the Hawaiian-Emperor bend developed, owing to flow in the deepest lower mantle associated with slab descent in the north and south Pacific.
Abstract: Neoproterozoic tectonic geography was dominated by the formation of the supercontinent Rodinia, its break-up and the subsequent amalgamation of Gondwana. The Neoproterozoic was a tumultuous time of Earth history, with large climatic variations, the emergence of complex life and a series of continent-building orogenies of a scale not repeated until the Cenozoic. Here we synthesise available geological and palaeomagnetic data and build the first full-plate, topological model of the Neoproterozoic that maps the evolution of the tectonic plate configurations during this time. Topological models trace evolving plate boundaries and facilitate the evaluation of “plate tectonic rules” such as subduction zone migration through time when building plate models. There is a rich history of subduction zone proxies preserved in the Neoproterozoic geological record, providing good evidence for the existence of continent-margin and intra-oceanic subduction zones through time. These are preserved either as volcanic arc protoliths accreted in continent-continent, or continent-arc collisions, or as the detritus of these volcanic arcs preserved in successor basins. Despite this, we find that the model presented here still predicts less subduction (ca. 90%) than on the modern earth, suggesting that we have produced a conservative model and are likely underestimating the amount of subduction, either due to a simplification of tectonically complex areas, or because of the absence of preservation in the geological record (e.g. ocean-ocean convergence). Furthermore, the reconstruction of plate boundary geometries provides constraints for global-scale earth system parameters, such as the role of volcanism or ridge production on the planet's icehouse climatic excursion during the Cryogenian. Besides modelling plate boundaries, our model presents some notable departures from previous Rodinia models. We omit India and South China from Rodinia completely, due to long-lived subduction preserved on margins of India and conflicting palaeomagnetic data for the Cryogenian, such that these two cratons act as ‘lonely wanderers’ for much of the Neoproterozoic. We also introduce a Tonian-Cryogenian aged rotation of the Congo-São Francisco Craton relative to Rodinia to better fit palaeomagnetic data and account for thick passive margin sediments along its southern margin during the Tonian. The GPlates files of the model are released to the public and it is our expectation that this model can act as a foundation for future model refinements, the testing of alternative models, as well as providing constraints for both geodynamic and palaeoclimate models.
Abstract: Volcanic hotspot tracks featuring linear progressions in the age of volcanism are typical surface expressions of plate tectonic movement on top of narrow plumes of hot material within Earth’s mantle1. Seismic imaging reveals that these plumes can be of deep origin2—probably rooted on thermochemical structures in the lower mantle3, 4, 5, 6. Although palaeomagnetic and radiometric age data suggest that mantle flow can advect plume conduits laterally7, 8, the flow dynamics underlying the formation of the sharp bend occurring only in the Hawaiian–Emperor hotspot track in the Pacific Ocean remains enigmatic. Here we present palaeogeographically constrained numerical models of thermochemical convection and demonstrate that flow in the deep lower mantle under the north Pacific was anomalously vigorous between 100 million years ago and 50 million years ago as a consequence of long-lasting subduction systems, unlike those in the south Pacific. These models show a sharp bend in the Hawaiian–Emperor hotspot track arising from the interplay of plume tilt and the lateral advection of plume sources. The different trajectories of the Hawaiian and Louisville hotspot tracks arise from asymmetric deformation of thermochemical structures under the Pacific between 100 million years ago and 50 million years ago. This asymmetric deformation waned just before the Hawaiian–Emperor bend developed, owing to flow in the deepest lower mantle associated with slab descent in the north and south Pacific.
Abstract: Neoproterozoic tectonic geography was dominated by the formation of the supercontinent Rodinia, its break-up and the subsequent amalgamation of Gondwana. The Neoproterozoic was a tumultuous time of Earth history, with large climatic variations, the emergence of complex life and a series of continent-building orogenies of a scale not repeated until the Cenozoic. Here we synthesise available geological and palaeomagnetic data and build the first full-plate, topological model of the Neoproterozoic that maps the evolution of the tectonic plate configurations during this time. Topological models trace evolving plate boundaries and facilitate the evaluation of “plate tectonic rules” such as subduction zone migration through time when building plate models. There is a rich history of subduction zone proxies preserved in the Neoproterozoic geological record, providing good evidence for the existence of continent-margin and intra-oceanic subduction zones through time. These are preserved either as volcanic arc protoliths accreted in continent-continent, or continent-arc collisions, or as the detritus of these volcanic arcs preserved in successor basins. Despite this, we find that the model presented here still predicts less subduction (ca. 90%) than on the modern earth, suggesting that we have produced a conservative model and are likely underestimating the amount of subduction, either due to a simplification of tectonically complex areas, or because of the absence of preservation in the geological record (e.g. ocean-ocean convergence). Furthermore, the reconstruction of plate boundary geometries provides constraints for global-scale earth system parameters, such as the role of volcanism or ridge production on the planet's icehouse climatic excursion during the Cryogenian. Besides modelling plate boundaries, our model presents some notable departures from previous Rodinia models. We omit India and South China from Rodinia completely, due to long-lived subduction preserved on margins of India and conflicting palaeomagnetic data for the Cryogenian, such that these two cratons act as ‘lonely wanderers’ for much of the Neoproterozoic. We also introduce a Tonian-Cryogenian aged rotation of the Congo-São Francisco Craton relative to Rodinia to better fit palaeomagnetic data and account for thick passive margin sediments along its southern margin during the Tonian. The GPlates files of the model are released to the public and it is our expectation that this model can act as a foundation for future model refinements, the testing of alternative models, as well as providing constraints for both geodynamic and palaeoclimate models.
Abstract: The extent of continental rifts and subduction zones through deep geological time provides insights into the mechanisms behind supercontinent cycles and the long term evolution of the mantle. However, previous compilations have stopped short of mapping the locations of rifts and subduction zones continuously since the Neoproterozoic and within a self-consistent plate kinematic framework. Using recently published plate models with continuously closing boundaries for the Neoproterozoic and Phanerozoic, we estimate how rift and peri-continental subduction length vary from 1 Ga to present and test hypotheses pertaining to the supercontinent cycle and supercontinent breakup. We extract measures of continental perimeter-to-area ratio as a proxy for the existence of a supercontinent, where during times of supercontinent existence the perimeter-to-area ratio should be low, and during assembly and dispersal it should be high. The amalgamation of Gondwana is clearly represented by changes in the length of peri-continental subduction and the breakup of Rodinia and Pangea by changes in rift lengths. The assembly of Pangea is not clearly defined using plate boundary lengths, likely because its formation resulted from the collision of only two large continents. Instead the assembly of Gondwana (ca. 520 Ma) marks the most prominent change in arc length and perimeter-to-area ratio during the last billion years suggesting that Gondwana during the Early Palaeozoic could explicitly be considered part of a Phanerozoic supercontinent. Consequently, the traditional understanding of the supercontinent cycle, in terms of supercontinent existence for short periods of time before dispersal and re-accretion, may be inadequate to fully describe the cycle. Instead, either a two-stage supercontinent cycle could be a more appropriate concept, or alternatively the time period of 1 to 0 Ga has to be considered as being dominated by supercontinent existence, with brief periods of dispersal and amalgamation.
Abstract: Global deep?time plate motion models have traditionally followed a classical rigid plate approach, even though plate deformation is known to be significant. Here we present a global Mesozoic?Cenozoic deforming plate motion model that captures the progressive extension of all continental margins since the initiation of rifting within Pangea at ~240 Ma. The model also includes major failed continental rifts and compressional deformation along collision zones. The outlines and timing of regional deformation episodes are reconstructed from a wealth of published regional tectonic models and associated geological and geophysical data. We reconstruct absolute plate motions in a mantle reference frame with a joint global inversion using hotspot tracks for the last 80 million years and minimizing global trench migration velocities and net lithospheric rotation. In our optimized model net rotation is consistently below 0.2°/Myr, and trench migration scatter is substantially reduced. Distributed plate deformation reaches a Mesozoic peak of 30 million km2 in the Late Jurassic (~160?155 Ma), driven by a vast network of rift systems. After a mid?Cretaceous drop in deformation it reaches a high of 48 million km2 in the Late Eocene (~35 Ma), driven by the progressive growth of plate collisions and the formation of new rift systems. About a third of the continental crustal area has been deformed since 240 Ma, partitioned roughly into 65% extension and 35% compression. This community plate model provides a framework for building detailed regional deforming plate networks and form a constraint for models of basin evolution and the plate?mantle system.
Muller, D., Zahirovic, S., Williams, S.E., Cannon, J., Seton, M., Bower, D.J., Tetley, M., Heine, C., Le Breton, E., Liu, S., Russell, S.H.J., Yang, T., Leonard, J., Gurnis, M.
Abstract: Global deep?time plate motion models have traditionally followed a classical rigid plate approach, even though plate deformation is known to be significant. Here we present a global Mesozoic-Cenozoic deforming plate motion model that captures the progressive extension of all continental margins since the initiation of rifting within Pangea at ~240 Ma. The model also includes major failed continental rifts and compressional deformation along collision zones. The outlines and timing of regional deformation episodes are reconstructed from a wealth of published regional tectonic models and associated geological and geophysical data. We reconstruct absolute plate motions in a mantle reference frame with a joint global inversion using hot spot tracks for the last 80 million years and minimizing global trench migration velocities and net lithospheric rotation. In our optimized model, net rotation is consistently below 0.2°/Myr, and trench migration scatter is substantially reduced. Distributed plate deformation reaches a Mesozoic peak of 30 × 106 km2 in the Late Jurassic (~160-155 Ma), driven by a vast network of rift systems. After a mid?Cretaceous drop in deformation, it reaches a high of 48 x 106 km2 in the Late Eocene (~35 Ma), driven by the progressive growth of plate collisions and the formation of new rift systems. About a third of the continental crustal area has been deformed since 240 Ma, partitioned roughly into 65% extension and 35% compression. This community plate model provides a framework for building detailed regional deforming plate networks and form a constraint for models of basin evolution and the plate?mantle system.
Abstract: Accurately mapping plate boundary types and locations through time is essential for understanding the evolution of the plate-mantle system and the exchange of material between the solid Earth and surface environments. However, the complexity of the Earth system and the cryptic nature of the geological record make it difficult to discriminate tectonic environments through deep time. Here we present a new method for identifying tectonic paleo-environments on Earth through a data mining approach using global geochemical data. We first fingerprint a variety of present-day tectonic environments utilising up to 136 geochemical data attributes in any available combination. A total of 38301 geochemical analyses from basalts aged from 5-0 Ma together with a well-established plate reconstruction model are used to construct a suite of discriminatory models for the first order tectonic environments of subduction and mid-ocean ridge as distinct from intraplate hotspot oceanic environments, identifying 41, 35, and 39 key discriminatory geochemical attributes, respectively. After training and validation, our model is applied to a global geochemical database of 1547 basalt samples of unknown tectonic origin aged between 1000-410 Ma, a relatively ill-constrained period of Earth's evolution following the breakup of the Rodinia supercontinent, producing 56 unique global tectonic environment predictions throughout the Neoproterozoic and Early Paleozoic. Predictions are used to discriminate between three alternative published Rodinia configuration models, identifying the model demonstrating the closest spatio-temporal consistency with the basalt record, and emphasizing the importance of integrating geochemical data into plate reconstructions. Our approach offers an extensible framework for constructing full-plate, deep-time reconstructions capable of assimilating a broad range of geochemical and geological observations, enabling next generation Earth system models.
Abstract: Accurately mapping plate boundary types and locations through time is essential for understanding the evolution of the plate-mantle system and the exchange of material between the solid Earth and surface environments. However, the complexity of the Earth system and the cryptic nature of the geological record make it difficult to discriminate tectonic environments through deep time. Here we present a new method for identifying tectonic paleo-environments on Earth through a data mining approach using global geochemical data. We first fingerprint a variety of present-day tectonic environments utilising up to 136 geochemical data attributes in any available combination. A total of 38301 geochemical analyses from basalts aged from 5-0 Ma together with a well-established plate reconstruction model are used to construct a suite of discriminatory models for the first order tectonic environments of subduction and mid-ocean ridge as distinct from intraplate hotspot oceanic environments, identifying 41, 35, and 39 key discriminatory geochemical attributes, respectively. After training and validation, our model is applied to a global geochemical database of 1547 basalt samples of unknown tectonic origin aged between 1000-410 Ma, a relatively ill-constrained period of Earth's evolution following the breakup of the Rodinia supercontinent, producing 56 unique global tectonic environment predictions throughout the Neoproterozoic and Early Paleozoic. Predictions are used to discriminate between three alternative published Rodinia configuration models, identifying the model demonstrating the closest spatio-temporal consistency with the basalt record, and emphasizing the importance of integrating geochemical data into plate reconstructions. Our approach offers an extensible framework for constructing full-plate, deep-time reconstructions capable of assimilating a broad range of geochemical and geological observations, enabling next generation Earth system models.
Journal of Geophysical Research Solid Earth, 10.1029/2019JB0 17442 28p. Pdf
Global
geodynamics
Abstract: The absolute motion of tectonic plates since Pangea can be derived from observations of hotspot trails, paleomagnetism, or seismic tomography. However, fitting observations is typically carried out in isolation without consideration for the fit to unused data or whether the resulting plate motions are geodynamically plausible. Through the joint evaluation of global hotspot track observations (for times <80 Ma), first?order estimates of net lithospheric rotation (NLR), and parameter estimation for paleo-trench migration (TM), we present a suite of geodynamically consistent, data?optimized global absolute reference frames from 220 Ma to the present. Each absolute plate motion (APM) model was evaluated against six published APM models, together incorporating the full range of primary data constraints. Model performance for published and new models was quantified through a standard statistical analyses using three key diagnostic global metrics: root?mean square plate velocities, NLR characteristics, and TM behavior. Additionally, models were assessed for consistency with published global paleomagnetic data and for ages <80 Ma for predicted relative hotspot motion, track geometry, and time dependence. Optimized APM models demonstrated significantly improved global fit with geological and geophysical observations while performing consistently with geodynamic constraints. Critically, APM models derived by limiting average rates of NLR to ~0.05°/Myr and absolute TM velocities to ~27?mm/year fit geological observations including hotspot tracks. This suggests that this range of NLR and TM estimates may be appropriate for Earth over the last 220 Myr, providing a key step toward the practical integration of numerical geodynamics into plate tectonic reconstructions.
Abstract: Recent progress in plate tectonic reconstructions has seen models move beyond the classical idea of continental drift by attempting to reconstruct the full evolving configuration of tectonic plates and plate boundaries. A particular problem for the Neoproterozoic and Cambrian is that many existing interpretations of geological and palaeomagnetic data have remained disconnected from younger, better-constrained periods in Earth history. An important test of deep time reconstructions is therefore to demonstrate the continuous kinematic viability of tectonic motions across multiple supercontinent cycles. We present, for the first time, a continuous full-plate model spanning 1 Ga to the present-day, that includes a revised and improved model for the Neoproterozoic-Cambrian (1000-520 Ma) that connects with models of the Phanerozoic, thereby opening up pre-Gondwana times for quantitative analysis and further regional refinements. In this contribution, we first summarise methodological approaches to full-plate modelling and review the existing full-plate models in order to select appropriate models that produce a single continuous model. Our model is presented in a palaeomagnetic reference frame, with a newly-derived apparent polar wander path for Gondwana from 540 to 320 Ma, and a global apparent polar wander path from 320 to 0 Ma. We stress, though while we have used palaeomagnetic data when available, the model is also geologically constrained, based on preserved data from past-plate boundaries. This study is intended as a first step in the direction of a detailed and self-consistent tectonic reconstruction for the last billion years of Earth history, and our model files are released to facilitate community development.
Earth Science Reviews , Vol. 214, 103477, 44p. Pdf
Mantle
plate tectonics, Rodinia, Gondwana
Abstract: Recent progress in plate tectonic reconstructions has seen models move beyond the classical idea of continental drift by attempting to reconstruct the full evolving configuration of tectonic plates and plate boundaries. A particular problem for the Neoproterozoic and Cambrian is that many existing interpretations of geological and palaeomagnetic data have remained disconnected from younger, better-constrained periods in Earth history. An important test of deep time reconstructions is therefore to demonstrate the continuous kinematic viability of tectonic motions across multiple supercontinent cycles. We present, for the first time, a continuous full-plate model spanning 1 Ga to the present-day, that includes a revised and improved model for the Neoproterozoic-Cambrian (1000-520 Ma) that connects with models of the Phanerozoic, thereby opening up pre-Gondwana times for quantitative analysis and further regional refinements. In this contribution, we first summarise methodological approaches to full-plate modelling and review the existing full-plate models in order to select appropriate models that produce a single continuous model. Our model is presented in a palaeomagnetic reference frame, with a newly-derived apparent polar wander path for Gondwana from 540 to 320 Ma, and a global apparent polar wander path from 320 to 0 Ma. We stress, though while we have used palaeomagnetic data when available, the model is also geologically constrained, based on preserved data from past-plate boundaries. This study is intended as a first step in the direction of a detailed and self-consistent tectonic reconstruction for the last billion years of Earth history, and our model files are released to facilitate community development.
Proceedings National Academy of Science, Vol. 116, pp. 407-412.
Australia
paleomagnetism
Abstract: Zircon crystals from the Jack Hills, Western Australia, are one of the few surviving mineralogical records of Earth’s first 500 million years and have been proposed to contain a paleomagnetic record of the Hadean geodynamo. A prerequisite for the preservation of Hadean magnetization is the presence of primary magnetic inclusions within pristine igneous zircon. To date no images of the magnetic recorders within ancient zircon have been presented. Here we use high-resolution transmission electron microscopy to demonstrate that all observed inclusions are secondary features formed via two distinct mechanisms. Magnetite is produced via a pipe-diffusion mechanism whereby iron diffuses into radiation-damaged zircon along the cores of dislocations and is precipitated inside nanopores and also during low-temperature recrystallization of radiation-damaged zircon in the presence of an aqueous fluid. Although these magnetites can be recognized as secondary using transmission electron microscopy, they otherwise occur in regions that are indistinguishable from pristine igneous zircon and carry remanent magnetization that postdates the crystallization age by at least several hundred million years. Without microscopic evidence ruling out secondary magnetite, the paleomagnetic case for a Hadean-Eoarchean geodynamo cannot yet been made.
The role of hydrothermal processes in the granite hosted Zirconium, Yttrium, rare earth elements (REE) deposit at Strange Lake, Quebec/Labrador: evidence from fluid inclusions
Geochimica et Cosmochimica Acta, Vol. 54, pp. 2403-2418
A reappraisal of the geology and geochemistry of the Zr-Y-Nb-Be and rare earth elements (REE)mineralized Strange Lake peralkalinepluton, Quebec-Labrador
Geological Association of Canada (GAC)/Mineralogical Association of Canada (MAC) Vancouver 90 Program with Abstracts, Held May 16-18, Vol. 15, p. A12. Abstract
Abstract: In response to rising demand of the rare earth elements (REE), recent exploration of the British Columbia alkaline province has identified the Wicheeda Carbonatite, which contains an estimated 11.3 million tons of light REE-enriched ore grading 1.95 wt.% TREO, to be the highest-grade prospect known in British Columbia. However, research of the deposit is restricted to one paper describing mineralization in carbonatite dikes adjacent to the main plug. This study describes the nature and origin of REEmineralization in the Wicheeda plug. The carbonatite was emplaced in metasedimentary limestone and argillaceous limestone belonging to the Kechika Group, which has been altered to potassic fenite immediately adjacent to the carbonatite and to sodic fenite at greater distances from it. The carbonatite comprises a ferroan dolomite core, which passes outwards gradationally into calcite carbonatite. Three texturally distinct varieties of dolomite have been recognized. Dolomite 1 constitutes most of the carbonatite; Dolomite 2 replaced Dolomite 1 near veins and vugs; Dolomite 3 occurs as a fracture and vug-lining phase with the REE mineralization. Stable carbon and oxygen isotopic ratios indicate that the calcite carbonatite is of mantle origin, that Dolomite 1 is of primary igneous origin, that Dolomite 2 is largely primary igneous with minor hydrothermal signature contamination, and that Dolomite 3 is of hydrothermal origin. Rare-metal mineralization in the deposit is, with the exception of pyrochlore, which occurs in the calcite carbonatite, restricted to veins and vugs in the dolomite carbonatite. There it occurs as hydrothermal veins and in vugs infilled by REE-fluorocarbonates, i.e., bastnäsite-(Ce), ancylite-(Ce), and monazite- (Ce) together with accessory pyrite, barite, molybdenite, and thorite. A model is proposed in which calcite carbonatite was the earliest magmatic phase to crystallize. The calcite carbonatite magma saturated with niobium relatively early, precipitating pyrochlore. The magma later evolved to a dolomite carbonatite composition which, upon cooling exsolved an aqueous carbonic fluid, which altered the Kechika metasediments to potassic fenite and mixed with formational waters further from the carbonatite to produce sodic fenite. This fluid mobilized the REE as chloride complexes into vugs and fractures in the dolomite carbonatite. Upon progressive fluid-rock interaction, the REE precipitated largely in response to cooling and pH. Hydrothermal concentration led to remarkable grade consistency, with virtually all of the dolomite carbonatite containing >1 wt.% TREO, making the Wicheeda Carbonatite a very attractive exploration target.
Journal of Geochemical Exploration, Vol. 188, pp. 194-215.
Canada, Northwest Territories
rare earths
Abstract: The Canadian Nechalacho rare metal deposit (Thor Lake, Northwest Territories) contains one of the of the world's largest high-grade resources of rare earth elements (REE) and a large niobium (Nb) resource (Avalon Rare Metals Inc., 2013). The deposit formed mainly by magmatic accumulation of eudialyte (a complex REE-Nb-zirconosilicate) at the top of a > 1.1 km deep and ~2 km diameter layered nepheline-sodalite syenite intrusion, the Nechalacho Layered Suite. The strongest enrichment of REE and Nb is contained in the eudialyte cumulates of the Basal Zone layer. However, a strong hydrothermal overprint modified the eudialyte cumulate layers and their host rocks to produce a variety of hydrothermal silicates and REE-Nb minerals. The primary objective of this study is to evaluate the spatial distribution of the alteration minerals and identify possible mineral zoning.
Abstract: Granites and pegmatites in the Strange Lake pluton underwent extreme enrichment in high field strength elements (HFSE), including the rare earth elements (REE). Much of this enrichment took place in the most altered rocks, and is expressed as secondary minerals, showing that hydrothermal fluids played an important role in HFSE concentration. Vasyukova et al. (2016) reconstructed a P-T-X path for the evolution of these fluids and provided evidence that hydrothermal activity was initiated by exsolution of fluid during crystallisation of border zone pegmatites (at ~450-500?°C and 1.1?kbar). This early fluid comprised a high salinity (25?wt% NaCl) aqueous phase and a CH4?+?H2 gas. During cooling, the gas was gradually oxidised, first to higher hydrocarbons (e.g., C2H6, C3H8), and then to CO2, and the salinity decreased to 4?wt% (~250-300?°C), before increasing to 19?wt%, due to fluid-rock interaction (~150?°C). Here, we present crush-leach fluid inclusion data on the concentrations of the REE and major ligands at different stages of the evolution of the fluid. The chondrite-normalised REE profile of the fluid evolved from light REE (La-Nd)-enriched at high temperature (~400?°C, Stages 1-2a) to middle REE (Sm-Er)-enriched at 360 to 250?°C (Stages 2b-3) and strongly heavy REE (Tm-Lu)-enriched at low temperature (150?°C, Stage 5). These changes in the REE distribution were accompanied by changes in the concentrations of major ligands, i.e., Cl? was the dominant ligand in Stages 1, 2, 4 and 5, whereas HCO3? was dominant in Stage 3. Alteration of arfvedsonite to aegirine and/or hematite contributed strongly to the mobilisation of the REE. This alteration released middle REE (MREE) and heavy REE (HREE), which either partitioned into the fluid or precipitated directly as bastnäsite-(Ce), ferri-allanite-(Ce) or gadolinite-(Y). Replacement of primary fluorbritholite-(Ce), which crystallised from an immiscible fluoride melt and altered to bastnäsite-(Ce), was also important in mobilising the REE (MREE). This paper presents the first report of the distribution of the REE in an evolving hydrothermal fluid. Using this distribution, in conjunction with information on the changing physicochemical conditions, the study identifies the sources of REE enrichment, reconstructs the path of REE concentration, and evaluates the REE mineralising capacity of the fluid. Finally, this information is integrated into a predictive model for REE mobilisation applicable not only to Strange Lake but any REE ore-forming system, in which hydrothermal processes were important.
Abstract: Large peralkaline complexes are ‘factories’ that have produced a variety of ‘exotic’ minerals including high field strength element minerals. In most cases, these minerals are secondary and crystallise in a hydrothermal paragenesis that is extremely difficult to decipher due to the complexity of the textural relationships. The Strange Lake pluton is one of these complexes, and contains 37 exotic minerals, most of which are secondary. Adding to the difficulty in establishing a comprehensive paragenesis for these minerals and an alteration/precipitation path for the pluton is the fact that there were several stages of crystallisation of the same exotic and common secondary minerals, e.g., bastnäsite, fluocerite, gadolinite, aegirine, fluorite, and zircon. In this paper, we present a model, which describes a detailed path for the alteration and precipitation of minerals in the closed hydrothermal system of a peralkaline granitic pegmatite, based on direct measurements of the evolving composition of the aqueous fluid that exsolved from the late-stage magma crystallising rare-metal pegmatites in the Strange Lake pluton. The driving force for this evolution was cooling-induced oxidation that ultimately transformed the CH4-H2 gas in this fluid to CO2. This led to a large drop in the pH, which was a major control on the composition of the fluid and the crystallisation of secondary minerals. Although large numbers of minerals formed and were replaced during the different stages of fluid evolution, the changing chemistry of the fluid was largely a response to the alteration of four minerals, namely arfvedsonite, elpidite, narsarsukite and fluorite. The earliest stage of alteration, which took place at ~360?°C, was marked by the replacement of arfvedsonite by aegirine. This alteration decreased salinity and released K, Li, and Rb to the fluid, causing K-metasomatism. At ~300?°C, CH4 and higher hydrocarbons reacted to produce CO2. This caused a massive drop in pH from a value?>?10 to a value of ~3 and intense alteration, which included the dissolution of fluorite, the breakdown of elpidite to zircon and quartz and the replacement of narsarsukite by titanite. With ongoing dissolution of fluorite, Ca activity reached a level sufficient to promote the alteration of elpidite to armstrongite or gittinsite. This was accompanied by alteration of arfvedsonite to ferroceladonite and microcline to Al-phyllosilicates, enriching the fluid in Na, Fe and F. Soon after, there was a near total loss of CO2 (at ~230?°C). This loss was catastrophic and was focused along conical fractures (these developed as a result of the collapse of the roof of the pluton), with resultant fragmentation of the rocks along the fluid path. Alteration to phyllosilicates continued after the loss of CO2, as the system cooled to ~190?°C. This marked the beginning of the final stage of alteration, which involved the replacement of arfvedsonite by aegirine and hematite. It also coincided with large scale hematisation within the pluton. Finally, it led to the cementation of the fragments along the fluid path to form the fluorite-hematite ring breccia that is now evident at the margins of the pluton. The model of fluid evolution presented here is potentially applicable to many other peralkaline complexes. The only requirements are that the system was closed until a relatively late stage and that the exsolved fluid was saline and contained a reduced carbonic component. This is a feature of many peralkaline complexes, most notably, the Khibiny and Lovozero complexes in Russia, and Ilímaussaq in Greenland.
Abstract: Granites and pegmatites in the Strange Lake pluton underwent extreme enrichment in high field strength elements (HFSE), including the rare earth elements (REE). Much of this enrichment took place in the most altered rocks, and is expressed as secondary minerals, showing that hydrothermal fluids played an important role in HFSE concentration. Vasyukova et al. (2016) reconstructed a P-T-X path for the evolution of these fluids and provided evidence that hydrothermal activity was initiated by exsolution of fluid during crystallisation of border zone pegmatites (at ~450-500?°C and 1.1?kbar). This early fluid comprised a high salinity (25?wt% NaCl) aqueous phase and a CH4?+?H2 gas. During cooling, the gas was gradually oxidised, first to higher hydrocarbons (e.g., C2H6, C3H8), and then to CO2, and the salinity decreased to 4?wt% (~250-300?°C), before increasing to 19?wt%, due to fluid-rock interaction (~150?°C). Here, we present crush-leach fluid inclusion data on the concentrations of the REE and major ligands at different stages of the evolution of the fluid. The chondrite-normalised REE profile of the fluid evolved from light REE (La-Nd)-enriched at high temperature (~400?°C, Stages 1-2a) to middle REE (Sm-Er)-enriched at 360 to 250?°C (Stages 2b-3) and strongly heavy REE (Tm-Lu)-enriched at low temperature (150?°C, Stage 5). These changes in the REE distribution were accompanied by changes in the concentrations of major ligands, i.e., Cl? was the dominant ligand in Stages 1, 2, 4 and 5, whereas HCO3? was dominant in Stage 3. Alteration of arfvedsonite to aegirine and/or hematite contributed strongly to the mobilisation of the REE. This alteration released middle REE (MREE) and heavy REE (HREE), which either partitioned into the fluid or precipitated directly as bastnäsite-(Ce), ferri-allanite-(Ce) or gadolinite-(Y). Replacement of primary fluorbritholite-(Ce), which crystallised from an immiscible fluoride melt and altered to bastnäsite-(Ce), was also important in mobilising the REE (MREE). This paper presents the first report of the distribution of the REE in an evolving hydrothermal fluid. Using this distribution, in conjunction with information on the changing physicochemical conditions, the study identifies the sources of REE enrichment, reconstructs the path of REE concentration, and evaluates the REE mineralising capacity of the fluid. Finally, this information is integrated into a predictive model for REE mobilisation applicable not only to Strange Lake but any REE ore-forming system, in which hydrothermal processes were important.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 71-72.
Canada, Nunavut
deposit - Chidliak
Abstract: The Chidliak exploration site was discovered in 2005 and acquired by De Beers Canada (De Beers) in September 2018. The Project is located on the Hall Peninsula of Baffin Island in the Qikiqtani Region of Nunavut and the closest communities are the Hamlet of Pangnirtung and the City of Iqaluit. The current Chidliak exploration site is not located within Inuit Owned Lands, Territorial or National Parks and is located entirely within Crown Lands. The current Chidliak exploration site includes 30 kimberlites two of which (CH-06 and CH-07) have been tested for grade and diamond value and are considered to be at an Inferred level of resource confidence. De Beers is currently engaged in a concept study to evaluate various FutureSmart Mining methods that would minimize environment impacts and enable relatively small kimberlites (diamond bearing rock) to be mined. De Beers is conducting desktop and field studies to evaluate options for mining methods, infrastructure, processing, information technology, and employee work models. In parallel, environmental field programs were conducted in 2019 to advance the environmental data collected in 2009 to 2017 and to support the evaluation of mining options. This presentation will provide a brief synopsis of the Project and work conducted in 2019 to advance the Project.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 72.
Canada, Northwest Territories
deposit - Snap Lake
Abstract: The Snap Lake Mine (the Mine) is a former underground diamond mine operated by De Beers Canada (De Beers), located about 220 kilometres northeast of Yellowknife in the Northwest Territories. The Snap Lake Mine operated from 2008 to 2015, and entered a Care and Maintenance mode in December 2015. In February 2017, the Mine underground workings were decommissioned and allowed to flood, in December 2017, De Beers announced the intent to enter into final closure, and in March 2019, De Beers submitted the Final Closure and Reclamation Plan for the Mine. Water management has always been an important component at the Mine and was considered in development of the Final Closure Plan to achieve the overall goal of “returning the site and affected areas around the Mine to technically viable and, where practicable, self-sustaining ecosystems that are compatible with a healthy environment and with human activities”. Water management at the Mine has changed significantly since diamond mining operations ceased. During diamond mining operations, a large volume of water was pumped from the underground to the surface for management and release to Snap Lake and the downstream environment. This mine water was relatively high in total dissolved solids and total suspended solids and therefore had to be treated prior to discharge. Now that the underground is flooded, there is no longer a need to pump mine water to the surface and water management has been greatly simplified. Since 2017, small volumes of runoff water from the North Pile (a surface disposal facility that was used for processed kimberlite, waste rock, and non-hazardous solid waste during operations) is collected for management and release to the underground and to Snap Lake. Water quality and aquatic ecosystem monitoring has been conducted yearly since pre-mining. Results of these programs have informed adaptive management at the site and informed plans for closure. The focus of this presentation is on water management and monitoring, for the Mine to the receiving environment, covering the history of the Mine to present and into planning for closure.
Peraluminous metamorphic rocks from the Namaqualand Metamorphic Complex (South Africa): geochem. evidence for an exhalation related sed. origin in a Mid.Prot
Chemical Geology, Vol. 81, No. 3, January 30, pp. 221-240
Lithospheric detachment and slab breakoff under the Variscan collisional orogen: keys to the origin of diamond bearing crustal rocks in the Bohemmian Massif.
18th. International Mineralogical Association Sept. 1-6, Edinburgh, abstract p.218.
Abstract: Hf-isotope data of >1100 detrital zircon grains from the Palaeozoic, south-central Andean Gondwana margin record the complete crustal evolution of South America, which was the predominant source. The oldest grains, with crustal residence ages of 3.8-4.0 Ga, are consistent with complete recycling of existing continental crust around 4 Ga. We confirm three major Archaean, Palaeoproterozoic (Transamazonian) and late Mesoproterozoic to early Neoproterozoic crust-addition phases as well as six igneous phases during Proterozoic to Palaeozoic time involving mixing of juvenile and crustally reworked material. A late Mesoproterozoic to early Neoproterozoic, Grenville-age igneous belt can be postulated along the palaeo-margin of South America. This belt was the basement for later magmatic arcs and accreted allochthonous microcontinents as recorded by similar crustal residence ages. Crustal reworking likely dominated over juvenile addition during the Palaeozoic era, and Proterozoic and Archaean zircon was mainly crustally reworked from the eroding, thickened Ordovician Famatinian arc.
Tappert, R., Foden, J., Muehlenbachs, K., Wills, K.
Garnet peridotite xenoliths and xenocrysts from the Monk Hill kimberlite, South Australia: insights into the lithospheric mantle beneath the Adelaide fold belt.
Journal of Petrology, Vol. 52, no. 10, pp. 1965-1986.
Journal of Volacnology and Geothermal Research, Vol. 373, pp. 68-96.
Australia, South Australia
deposit - Eurelia
Abstract: Kimberlites of Jurassic age occur in various parts of South Australia. Thirty-nine of these kimberlites, which are mostly new discoveries, were studied to characterize their structural setting, their petrography, and the composition of their constituent minerals. Although some of the kimberlites in South Australia occur on the Archean to Paleoproterozoic Gawler Block, most are part of a northwest-trending, semi-continuous kimberlite dike swarm located in the Adelaide Fold Belt. The kimberlites typically occur as dikes or sills, but diatremes are also present. In the Adelaide Fold Belt, diatremes are restricted to the hinge zones of regional-scale folds within thick sedimentary sequences of the Adelaidean Supergroup. Despite widespread and severe alteration, coherent and pyroclastic kimberlites can be readily distinguished. U-Pb and Sr/Nd isotopic compositions of groundmass perovskite indicate that all kimberlites belong to the same age group (177-197?Ma) and formed in a near-primitive mantle environment (87Sr/86Sr: 0.7038-0.7052, ?Nd: ?0.07 to +2.97). However, the kimberlites in South Australia are compositionally diverse, and range from olivine-dominated varieties (macrocrystic kimberlites) to olivine-poor, phlogopite-dominated varieties (micaceous kimberlites). Macrocrystic kimberlites contain magnesium-rich groundmass phlogopite and spinel, and they are typically olivine macrocryst-rich. Micaceous kimberlites, in contrast, contain more iron- and titanium-rich groundmass phlogopite and less magnesian spinel, and olivine macrocrysts are rare or absent. Correlations between phlogopite and spinel compositions with modal abundances of olivine, indicate that the contrast between macrocrystic and micaceous kimberlites is primarily linked to the amount of mantle components that were incorporated into a compositionally uniform parental mafic silicate melt. We propose that assimilation of xenocrystic magnesite and incorporation of xenocrystic olivine from dunitic source rocks were the key processes that modified the parental silicate melt and created the unique hybrid (carbonate-silicate) character of kimberlites. Based on the composition of xenoliths and xenocrysts, the lithospheric mantle sampled by the South Australian kimberlites is relatively uniform, and extends to depths of 160-170?km, which is slightly below the diamond stability field. Only beneath the Eurelia area does the lithosphere appear thicker (>175?km), which is consistent with the presence of diamonds in some of the Eurelia kimberlites.
Journal of South American Earth Sciences, Vol. 70, pp. 162-173.
South America
Craton
Abstract: The Amazonian craton, which covers a large area of South America, and is thought to have been stable since the end of the Mesoproterozoic, has recently benefited from a series of regional geophysical surveys. The Amazonian craton comprises the northern Guyana shield and the southern Central Brazil shield. It has become the main subject of seismological studies aiming to determine crustal thickness. Moho thickness maps that cover a large part of the South American continent summarize these studies. Receiver function studies, aided by surface wave dispersion tomography, were also useful tools applied in the region over the past decade. These have been improved by the addition of temporary and permanent regional seismological arrays and stations. An interesting NNW-SSE Moho depth anomaly, pointing to crustal thickening of up to 60 km in the central Guyana shield and a 50 km thick anomaly of the southern Central Brazil shield were recently identified. Areas with crustal thickening correspond to Paleoproterozoic magmatic arcs. The upper mantle seismic anisotropy in part of the region has been determined from SKS splitting studies. The currently available seismic anisotropy information shows that the orientation of the determined anisotropic axis is related to the frozen in anisotropy hypothesis for the Amazonian craton. The orientation of the anisotropic axis shows no relation to the current South American plate motion in the Amazonian craton. Most recently, detailed information for the two shields has benefited from a series of high-resolution, regional aerogeophysical surveys, made available by CPRM, the Brazilian Geological Survey. In addition to the mentioned contribution from seismology for imaging deeper crustal structures, regional gravity surveys have been expanded, adding to previous Bouguer anomaly maps, and deep drilling information from early exploration efforts have been compiled for the Amazon basin, which covers the Amazonian craton separating the Guyana and Central Brazil shields.
The South African Gold Fields Where they Are, What they Area and the Best Route to Them. with a Section by J. B. Moodieon the Diamond Fields of South Africa and How to Reach Them.
Abstract: Hf-isotope data of greater than 1100 detrital zircon grains from the Palaeozoic, south-central Andean Gondwana margin record the complete crustal evolution of South America, which was the predominant source. The oldest grains, with crustal residence ages of 3.8-4.0 Ga, are consistent with complete recycling of existing continental crust around 4 Ga. We confirm three major Archaean, Palaeoproterozoic (Transamazonian) and late Mesoproterozoic to early Neoproterozoic crust-addition phases as well as six igneous phases during Proterozoic to Palaeozoic time involving mixing of juvenile and crustally reworked material. A late Mesoproterozoic to early Neoproterozoic, Grenville-age igneous belt can be postulated along the palaeo-margin of South America. This belt was the basement for later magmatic arcs and accreted allochthonous microcontinents as recorded by similar crustal residence ages. Crustal reworking likely dominated over juvenile addition during the Palaeozoic era, and Proterozoic and Archaean zircons were mainly crustally reworked from the eroding, thickened Ordovician Famatinian arc.
Kleinhanns, I.C., Fullgraf, T., Wilsky, F., Nolte, N., Fliegel, D., Klemd, R., Hansen, B.T.
U-Pb zircon ages and (isotope) geochemical signatures of the Kamanjab In lier ( NW Namibia): constraints on Palaeoproterozoic crustal evolution along the southern Congo craton.
Geological Society of London Special Publication: Continent formation through time., No. 389, pp. 165-195.
Geological Society of London Special Publications, doi:https://dori.org/10.1144/SP513-2021-84 30p. Pdf proof
Africa, South Africa
lamproite
Abstract: Orangeites are a significant source of diamonds, yet ambiguity surrounds their status among groups of mantle-derived potassic rocks. This study reports mineralogical and geochemical data for a ca. 140 Ma orangeite dyke swarm that intersects the Bushveld Complex on the Kaapvaal craton in South Africa. The dykes comprise distinctive petrographic varieties that are linked principally by olivine fractionation, with the most evolved members containing minor amounts of primary carbonate, sanidine and andradite garnet in the groundmass. Although abundant groundmass phlogopite and clinopyroxene have compositions that are similar to those of cratonic lamproites, these phases show notable Ti-depletion, which we consider a hallmark feature of type orangeites from the Kaapvaal craton. Ti-depletion is also characteristic for the bulk rock compositions and is associated with strongly depleted Th-U-Nb-Ta contents at high Cs-Rb-Ba-K concentrations. The resultant high LILE/HFSE ratios of orangeites suggest that mantle source enrichment occurred by metasomatic processes in the proximity of ancient subduction zones. The Bushveld-intersecting orangeite dykes have strongly enriched Sr-Nd-Hf isotopic compositions (initial 87Sr/86Sr = 0.70701-0.70741; ?Nd = ?10.6 to ?5.8; ?Hf = ?14.4 to ?2.5), similar to those of other orangeites from across South Africa. Combined with the strong Ti-Nb-Ta depletion, this ubiquitous isotopic feature points to the involvement of ancient metasomatized mantle lithosphere in the origin of Kaapvaal craton orangeites, where K-rich metasomes imparted a ‘fossil’ subduction geochemical signature. Previous geochronology studies identified ancient K-enrichment events within the Kaapvaal cratonic mantle lithosphere, possibly associated with collisional tectonics during the 1.2-1.1 Ga Namaqua-Natal orogeny of the Rodinia supercontinent cycle. It therefore seems permissible that the cratonic mantle root was preconditioned for ultrapotassic magma production by tectonomagmatic events that occurred along convergent plate margins during the Proterozoic. However, reactivation of the K-rich metasomes had to await establishment of an extensional tectonic regime, such as that during the Mesozoic breakup of Gondwana, which was accompanied by widespread (1000 × 750 km) small-volume orangeite volcanism between 200 and 110 Ma. Although similarities exist between orangeites and lamproites, these and other potassic rocks are sufficiently distinct in their compositions such that different magma formation processes must be considered. In addition to new investigations of the geodynamic triggers of K-rich ultramafic magmatism, future research should more stringently evaluate the relative roles of redox effects and volatile components such as H2O-CO2-F in the petrogeneses of these potentially diamondiferous alkaline rocks.
Earth and Planetary Science Letters, Vol. 547, 14p. Pdf
Africa
LLSVP, superplume
Abstract: Many volcanic hotspots are connected via ‘plume’ conduits to thermochemical structures with anomalously low seismic velocities at the core-mantle boundary. Basaltic lavas from some of these hotspots show anomalous daughter isotope abundances for the short-lived 129I-129Xe, 146Sm-142Nd, and 182Hf-182W radioactive decay systems, suggesting that their lower mantle sources contain material that dates back to Earth-forming events during the first 100 million years in solar system history. Survival of such ‘primordial’ remnants in Earth's mantle places important constraints on the evolution and inner workings of terrestrial planets. Here we report high-precision 182W/184W measurements for a large suite of kimberlite volcanic rocks from across the African tectonic plate, which for the past 250 million years has drifted over the most prominent thermochemical seismic anomaly at the core-mantle boundary. This so-called African LLSVP, or ‘large low shear-wave velocity province’, is widely suspected to store early Earth remnants and is implicated as the ultimate source of global Phanerozoic kimberlite magmatism. Our results show, however, that kimberlites from above the African LLSVP, including localities with lower mantle diamonds such as Letseng and Karowe Orapa A/K6, lack anomalous 182W signatures, with an average W value of 0.0 ± 4.1 (2SD) for the 18 occurrences studied. If kimberlites are indeed sourced from the African LLSVP or superplume, then the extensive 182W evidence suggests that primordial or core-equilibrated mantle materials, which may contribute resolvable W excesses or deficits, are only minor or locally concentrated components in the lowermost mantle, for example in the much smaller ‘ultra-low velocity zones’ or ULVZs. However, the lack of anomalous 182W may simply suggest that low-volume kimberlite magmas are not derived from hot lower mantle plumes. In this alternative scenario, kimberlite magmas originate from volatile-fluxed ambient convecting upper mantle domains beneath relatively thick and cold lithosphere from where previously ‘stranded’ lower mantle and transition zone diamonds can be plucked.
Emplacement, crystallization and alteration of spinifex textured komatiitic basalt flows in the Archean Nondweni greenstone belt, southern Kaapvaal craton, South Afr
Contributions to Mineralogy and Petrology, Vol. 101, pp. 301-317. Database # 17781
The geology of the Great Dyke, Zimbabwe: crystallization, layering, and cumulate formation in the P1 pyroxenite of cyclic Unit I of the Dawendalesubchamber
Abstract: H2O strongly influences physical properties of the mantle and its ability to melt or convect and can trace recycling of surface reservoirs down to the deep mantle1,2. This makes knowledge of water content in the Earth's interior and its evolution through time crucial to understanding global geodynamics. Komatiites (MgO-rich ultramafic magmas) result from high-degree mantle melting at high pressures3 and thus are excellent probes of H2O contents in the deep mantle. A significant excess of H2O over elements of similar geochemical behavior during mantle melting (e.g. Ce) was recently found in melt inclusions in the most Mg-rich olivine in 2.7 Ga old komatiites from Canada4 and Zimbabwe5. These data were taken as evidence for a deep hydrated mantle reservoir, probably the transition zone, in the Neoarchean time. In this paper we confirm the mantle source of this H2O by measurement of deuterium to hydrogen ratios in these melt inclusions and present similar data for 3.3 Ga old komatiites from the Barberton Greenstone Belt. Using hydrogen isotopes, we show that the mantle sources of these melts contained excess H2O which implies that a deep mantle hydrated reservoir has been present in the Earth's interior at least since the Paleoarchean. The reconstructed initial hydrogen isotope composition of komatiites is significantly more depleted in deuterium than all surface reservoirs and typical mantle but resembles that in dehydrated subducted slabs. Together with a significant excess of chlorine and a temporal trend of Pb/Ce in the mantle sources of komatiites, these results argue that lithosphere recycling into the deep mantle, arguably via subduction, started before 3.3 Ga. (a un-reviewed version of the manuscript accepted for publication in Nature magazine).
Geological Society of London Special Publication 513, pp. 17-44.
Africa, South Africa
lamproites
Abstract: Orangeites are a significant source of diamonds, yet ambiguity surrounds their status among groups of mantle-derived potassic rocks. This study reports mineralogical and geochemical data for a c. 140 Ma orangeite dyke swarm that intersects the Bushveld Complex on the Kaapvaal craton in South Africa. The dykes comprise distinctive petrographic varieties that are linked principally by olivine fractionation, with the most evolved members containing minor amounts of primary carbonate, sanidine and andradite garnet in the groundmass. Although abundant groundmass phlogopite and clinopyroxene have compositions that are similar to those of cratonic lamproites, these phases show notable Ti-depletion, which we consider a hallmark feature of type orangeites from the Kaapvaal craton. Ti-depletion is also characteristic of bulk rock compositions and is associated with strongly depleted Th-U-Nb-Ta contents at high Cs-Rb-Ba-K concentrations. The resultant high large ion lithophile element/high field strength element ratios of orangeites suggest that mantle source enrichment occurred by metasomatic processes in the proximity of ancient subduction zones. The Bushveld-intersecting orangeite dykes have strongly enriched Sr-Nd-Hf isotopic compositions (initial 87Sr/86Sr = 0.70701-0.70741; ?Nd = ?10.6 to ?5.8; ?Hf = ?14.4 to ?2.5), similar to those of other orangeites from across South Africa. Combined with the strong Ti-Nb-Ta depletion, this ubiquitous isotopic feature points to the involvement of ancient metasomatized mantle lithosphere in the origin of Kaapvaal craton orangeites, where K-rich metasomes imparted a ‘fossil’ subduction geochemical signature. Previous geochronology studies identified ancient K-enrichment events within the Kaapvaal cratonic mantle lithosphere, possibly associated with collisional tectonics during the 1.2-1.1 Ga Namaqua-Natal orogeny of the Rodinia supercontinent cycle. It therefore seems permissible that the cratonic mantle root was preconditioned for ultrapotassic magma production by tectonomagmatic events that occurred along convergent plate margins during the Proterozoic. However, reactivation of the K-rich metasomes had to await establishment of an extensional tectonic regime, such as that during the Mesozoic breakup of Gondwana, which was accompanied by widespread (1000 × 750 km) small-volume orangeite volcanism between 200 and 110 Ma. Although similarities exist between orangeites and lamproites, these and other potassic rocks are sufficiently distinct in their compositions such that different magma formation processes must be considered. In addition to new investigations of the geodynamic triggers of K-rich ultramafic magmatism, future research should more stringently evaluate the relative roles of redox effects and volatile components such as H2O-CO2-F in the petrogeneses of these potentially diamondiferous alkaline rocks.
Abstract: Over the last 20 years, new concepts have emerged into understanding the processes that lead to build up to large silicic explosive eruptions based on integration of geophysical, geochemical, petrological, geochronological and dynamical modelling. Silicic melts are generated within magma systems extending throughout the crust by segregation from mushy zones. Segregated melt layers become unstable and can assemble into ephemeral upper crustal magma chambers rapidly prior to eruption. In the next 10 years, we can expect major advances in dynamical models as well as in analytical and geophysical methods, which need to be underpinned in field research.
Earth and Planetary Science Letters, Vol. 434, pp. 10-17.
Mantle
Tectonics
Abstract: It has been proposed that the spatial variations recorded in the geochemistry of hotspot lavas, such as the bilateral asymmetry recorded at Hawaii, can be directly mapped as the heterogeneous structure and composition of their deep-mantle source. This would imply that source-region heterogeneities are transported into, and preserved within, a plume conduit, as the plume rises from the deep-mantle to Earth's surface. Previous laboratory and numerical studies, which neglect density and rheological variations between different chemical components, support this view. However, in this paper, we demonstrate that this interpretation cannot be extended to distinct chemical domains that differ from surrounding mantle in their density and viscosity. By numerically simulating thermo-chemical mantle plumes across a broad parameter space, in 2-D and 3-D, we identify two conduit structures: (i) bilaterally asymmetric conduits, which occur exclusively for cases where the chemical effect on buoyancy is negligible, in which the spatial distribution of deep-mantle heterogeneities is preserved during plume ascent; and (ii) concentric conduits, which occur for all other cases, with dense material preferentially sampled within the conduit's centre. In the latter regime, the spatial distribution of geochemical domains in the lowermost mantle is not preserved during plume ascent. Our results imply that the heterogeneous structure and composition of Earth's lowermost mantle can only be mapped from geochemical observations at Earth's surface if chemical heterogeneity is a passive component of lowermost mantle dynamics (i.e. its effect on density is outweighed by, or is secondary to, the effect of temperature). The implications of our results for: (i) why oceanic crust should be the prevalent component of ocean island basalts; and (ii) how we interpret the geochemical evolution of Earth's deep-mantle are also discussed.
Journal of Geophysical Research: Solid Earth, Vol. 122, 8, pp. 6247-6288.
Mantle
mineralogy
Abstract: Mineral grain size in the mantle affects fluid migration by controlling mantle permeability; the smaller the grain size, the less permeable the mantle is. Mantle shear viscosity also affects fluid migration by controlling compaction pressure; high mantle shear viscosity can act as a barrier to fluid flow. Here we investigate for the first time their combined effects on fluid migration in the mantle wedge of subduction zones over ranges of subduction parameters and patterns of fluid influx using a 2-D numerical fluid migration model. Our results show that fluids introduced into the mantle wedge beneath the forearc are first dragged downdip by the mantle flow due to small grain size (<1 mm) and high mantle shear viscosity that develop along the base of the mantle wedge. Increasing grain size with depth allows upward fluid migration out of the high shear viscosity layer at subarc depths. Fluids introduced into the mantle wedge at postarc depths migrate upward due to relatively large grain size in the deep mantle wedge, forming secondary fluid pathways behind the arc. Fluids that reach the shallow part of the mantle wedge spread trench-ward due to the combined effect of high mantle shear viscosity and advection by the inflowing mantle and eventually pond at 55-65 km depths. These results show that grain size and mantle shear viscosity together play an important role in focusing fluids beneath the arc.
Abstract: Earth’s surface topography is a direct physical expression of our planet’s dynamics. Most is isostatic, controlled by thickness and density variations within the crust and lithosphere, but a substantial proportion arises from forces exerted by underlying mantle convection. This dynamic topography directly connects the evolution of surface environments to Earth’s deep interior, but predictions from mantle flow simulations are often inconsistent with inferences from the geological record, with little consensus about its spatial pattern, wavelength and amplitude. Here, we demonstrate that previous comparisons between predictive models and observational constraints have been biased by subjective choices. Using measurements of residual topography beneath the oceans, and a hierarchical Bayesian approach to performing spherical harmonic analyses, we generate a robust estimate of Earth’s oceanic residual topography power spectrum. This indicates water-loaded power of 0.5?±?0.35?km2 and peak amplitudes of up to ~0.8?±?0.1?km at long wavelengths (~104?km), decreasing by roughly one order of magnitude at shorter wavelengths (~103?km). We show that geodynamical simulations can be reconciled with observational constraints only if they incorporate lithospheric structure and its impact on mantle flow. This demonstrates that both deep (long-wavelength) and shallow (shorter-wavelength) processes are crucial, and implies that dynamic topography is intimately connected to the structure and evolution of Earth’s lithosphere.
Circumferential Faulting Around Wells Creek Basin, Houston And Stewart Counties, Tennessee- a Manuscript by Safford, J.m. and Lander, D.w.t. : Circa 1895.
Tennessee Academy of Science Journal, Vol. 41, No. 1, PP. 37-48.
Global
Kimberlite, Western Tennessee, Central States, Cryptoexplosion
Abstract: The Diavik Waste Rock Project consists of laboratory and field experiments developed for the investigation and scale-up of the geochemical evolution of sulfidic mine wastes. As part of this project, humidity cell experiments were conducted to assess the long-term geochemical evolution of a low-sulfide waste rock. Reactive transport modelling was used to assess the significant geochemical processes controlling oxidation of sulfide minerals and their dependence on temperature and sulfide mineral content. The geochemical evolution of effluent from waste rock with a sulfide content of 0.16 wt.% and 0.02 wt.% in humidity cells was simulated with the reactive transport model MIN3P, based on a conceptual model that included constant water flow, sulfide mineral content, sulfide oxidation controlled by the availability of oxidants, and subsequent neutralization reactions with carbonate and aluminosilicate minerals. Concentrations of Ni, Co, Cu, Zn, and SO4 in the humidity cell effluent were simulated using the shrinking core model, which represented the control of oxidant diffusion to the unreacted particle surface in the sulfide oxidation process. The influence of temperature was accounted for using the Arrhenius relation and appropriate activation energy values. Comparison of the experiment results, consisting of waste rock differentiated by sulfide mineral content and temperature, indicated surface area and temperature play important roles in rates of sulfide oxidation and release of sulfate and metals. After the model was calibrated to fit the effluent data from the higher sulfide content cells, subsequent simulations were conducted by adjusting only measured parameters, including sulfide mineral content and surface area.
Abstract: The Diavik Waste Rock Project, located in a region of continuous permafrost in northern Canada, includes complementary field and laboratory experiments with the purpose of investigating scale-up techniques for the assessment of the geochemical evolution of mine waste rock at a large scale. As part of the Diavik project, medium-scale field experiments (?1.5?m high active zone lysimeters) were conducted to assess the long term geochemical evolution and drainage of a low-sulfide waste rock under a relatively simple (i.e. constrained by the container) flow regime while exposed to atmospheric conditions. A conceptual model, including the most significant processes controlling the sulfide-mineral oxidation and weathering of the associated host minerals as observed in a laboratory humidity cell experiment, was developed as part of a previous modelling study. The current study investigated the efficacy of scaling the calibrated humidity cell model to simulate the geochemical evolution of the active zone lysimeter experiments. The humidity cell model was used to simulate the geochemical evolution of low-sulfide waste rock with S content of 0.053?wt.% and 0.035?wt.% (primarily pyrrhotite) in the active zone lysimeter experiments using the reactive transport code MIN3P. Water flow through the lysimeters was simulated using temporally variable infiltration estimated from precipitation measurements made within 200?m of the lysimeters. Flow parameters and physical properties determined during previous studies at Diavik were incorporated into the simulations to reproduce the flow regime. The geochemical evolution of the waste-rock system was simulated by adjustment of the sulfide-mineral content to reflect the values measured at the lysimeters. The temperature dependence of the geochemical system was considered using temperature measurements taken daily, adjacent to the lysimeters, to correct weathering rates according to the Arrhenius equation. The lysimeter simulations indicated that a model developed from simulations of laboratory humidity cell experiments, incorporating detailed representations of temporally variable temperature and water infiltration, can be scaled to provide a reasonable assessment of geochemical evolution of the medium-scale field experiments.
Abstract: The geochemical evolution of mine-waste rock often includes concurrent acid generation and neutralization processes. Deposition of mine-waste rock in large, oxygenated, and partially saturated piles can result in release of metals and decreased pH from weathering of sulfide minerals. Acid neutralization processes can often mitigate metals and pH impacts associated with sulfide oxidation. The Diavik Waste Rock Project included large field experiments (test piles built in 2006) conducted to characterize weathering of sulfide waste rock at a scale representative of full size waste-rock piles. Water samples from the unsaturated interior of one of the test piles, constructed of waste rock with ~0.05 wt.% S, were collected using soil water solution samplers and drains at the base of the pile. Field observations indicated pH decreased throughout the depth of the pile during 2008 and 2009 and that carbonate mineral buffering was entirely depleted by 2011 or 2012. Carbonate mineral exhaustion was accompanied by increased concentrations of dissolved Al and Fe in effluent samples collected at the basal drains. These results suggest that dissolution of Al and Fe(oxy)hydroxides occurred after the depletion of carbonate minerals following an acid neutralization sequence that is similar to observations made by previous researchers. A conceptual model of acid neutralization proceses within the pile, developed using physical and geochemical measurements conducted from 2008 to 2012, was used to inform reactive transport simulations conducted in 2017 to quantify the dominant acid neutralization processes within the test pile interior. Reactive transport simulations indicate that the conceptual model developed using the results of field samples provides a reasonable assessment of the evolution of the acid neutralization sequence.
The relationship of remote sensing anomalies to the real world-examples from the midcontinent and the CUSMAP study areas
United States Geological Survey (USGS) Open file, United States Geological Survey (USGS)-Missouri G.S. Symp: Mineral resource potential of, p. 45. (abstract.)
Nuclear instruments and methods in Physics Research Section B , Vol. 123 ( 1-4) pp. 579-582.
Technology
spectrometry
Abstract: A brief overview is provided of the uses of AMS in mineral analysis, emphasizing the selection of appropriate samples. Simple guidelines are given for judging the suitability of a set of samples (and the type of problem that they pose) for AMS, as opposed to other methods of in-situ analysis. Optimal interpretation of the AMS data requires that the method be employed in conjunction with a range of other types of information. These include textural and mineralogical observations obtained with petrographic or scanning electron microscopes, plus in-situ chemical data for areas of the target typically 1–250 ?m in diameter, obtained by some combination of complementary techniques, such as electron, proton or ion microprobe analysis (EPM, PIXE and SIMS, respectively).
A craton and its cracks: some of the behaviour of the Zimbabwe block From the Late Archaean to the Mesozoic in response to horiz. movements, and sign.mafic dykes
Journal of African Earth Sciences, Vol. 10, No. 3, pp. 483-501
Post collisional, potassic and ultrapotassic magmatism of the northern Tibetan Plateau: constraints on characteristics of the mantle source, geodynamic uplift
Stable isotope composition of magmatic and deuteric carbonate phases in hypabyssal kimberlite, Lac de Gras field: implications for the composition of fluids...
Abstract: Rare earth element (REE) orebodies are typically associated with alkaline igneous rocks or develop as placer or laterite deposits. Here, we describe an economically important heavy (H)REE mineralization type that is entirely hydrothermal in origin with no demonstrable links to magmatism. The mineralization occurs as numerous xenotime-rich vein and breccia orebodies across a large area of northern Australia but particularly close to a regional unconformity between Archean metasedimentary rocks of the Browns Range Metamorphics and overlying Proterozoic sandstones of the Birrindudu Group. The deposits formed at 1.65 to 1.61 Ga along steeply dipping faults; there is no known local igneous activity at this time. Depletion of HREEs in the Browns Range Metamorphics, together with the similar nonradiogenic Nd isotope composition of the orebodies and the Browns Range Metamorphics, indicates that ore metals were leached directly from the Browns Range metasedimentary rocks. We propose an ore genesis model that involves fluid leaching HREEs from the Browns Range Metamorphics and subsequently mixing with P-bearing acidic fluid from the overlying sandstones in fault zones near the unconformity. The union of P and HREEs via fluid mixing in a low-Ca environment triggered extensive xenotime precipitation. This mineralization is unlike that of any other class of REE ore deposit but has a similar setting to unconformity-related U deposits of Australia and Canada, so we assign it the label “unconformity-related REE.” Further discoveries of this REE mineralization type are expected near regional unconformities within Proterozoic intracontinental sedimentary basins across the globe.
IN: Cycle Concepts in Plate Tectonics, editors Wilson and Houseman , Geological Society of London special publication 470, pp. 1-17. pdf
Mantle
plate tectonics
Abstract: It is now more than 50 years since Tuzo Wilson published his paper asking ‘Did the Atlantic close and then re-open?’. This led to the ‘Wilson Cycle’ concept in which the repeated opening and closing of ocean basins along old orogenic belts is a key process in the assembly and breakup of supercontinents. This implied that the processes of rifting and mountain building somehow pre-conditioned and weakened the lithosphere in these regions, making them susceptible to strain localization during future deformation episodes. Here we provide a retrospective look at the development of the concept, how it has evolved over the past five decades, current thinking and future focus areas. The Wilson Cycle has proved enormously important to the theory and practice of geology and underlies much of what we know about the geological evolution of the Earth and its lithosphere. The concept will no doubt continue to be developed as we gain more understanding of the physical processes that control mantle convection and plate tectonics, and as more data become available from currently less accessible regions.
Quantifying carbon fixation in trace minerals from processed kimberlite: a comparative study of quantitative methods using X-ray powder diffraction data
Mineralogy and Petrology, 10.1007/ s00710-018- 0589-4, 14p.
Africa, South Africa, Canada, Northwest Territories, Ontario
deposit - Venetia, Voorspoed, Gahcho Kue, Victor, Snap Lake
Abstract: De Beers kimberlite mine operations in South Africa (Venetia and Voorspoed) and Canada (Gahcho Kué, Victor, and Snap Lake) have the potential to sequester carbon dioxide (CO2) through weathering of kimberlite mine tailings, which can store carbon in secondary carbonate minerals (mineral carbonation). Carbonation of ca. 4.7 to 24.0 wt% (average?=?13.8 wt%) of annual processed kimberlite production could offset 100% of each mine site’s carbon dioxide equivalent (CO2e) emissions. Minerals of particular interest for reactivity with atmospheric or waste CO2 from energy production include serpentine minerals, olivine (forsterite), brucite, and smectite. The most abundant minerals, such as serpentine polymorphs, provide the bulk of the carbonation potential. However, the detection of minor amounts of highly reactive brucite in tailings from Victor, as well as the likely presence of brucite at Venetia, Gahcho Kué, and Snap Lake, is also important for the mineral carbonation potential of the mine sites.
Abstract: Mineral carbonation is a form of carbon capture, utilization and storage (CCUS) that aims to transform excess CO2 into environmentally benign carbonate minerals which are geologically stable. Here, we investigated the reactivity of processed kimberlite and kimberlite ore from the Venetia Diamond Mine (South Africa). Highly reactive phases, such as brucite [Mg(OH)2], are uncommon in the samples collected from Venetia necessitating the development of new strategies for mineral carbonation. Kimberlite ore and tailings from this mine consist of a clay-rich mineral assemblage that is dominated by lizardite (a serpentine mineral) and smectites. Smectites are swelling clays that can act as a source of Mg and Ca for carbonation reactions via cation exchange, dissolution and/or direct replacement of smectites to form carbonate phases. Although carbonation of serpentine and brucite has long been a focus of CCUS in mine wastes [1], smectite carbonation has not been explored in this setting. Quantitative X-ray diffraction using Rietveld refinements coupled with Fourier-transform infrared spectroscopy indicate that smectites of stevensite-saponite composition are abundant in the Venetia samples (1.3-15.4 wt.%). Synchrotron-based X-ray fluorescence mapping correlated with scanning and transmission electron microscopy show that smectites are distributed as altered, smooth regions measuring from 1 to 20 ?m in breadth. These phases are rich in Mg and Ca and Al-poor. To better understand the behaviour/reactivity of smectites during the cation exchange process, we have used batch experiments with pure endmembers of Ca-, Mg- and Na-montmorillonite under different treatment conditions (NH4-citrate, NH4-O-acetate, NH4-Cl and Na3-citrate). After 24 hours of reaction, ICP-MS analyses reveal that the four treatments have the same efficiency for Ca and Mg exchange, while NH4-Cl and NH4- O-acetate treatments minimize calcite dissolution. Our end goals are to optimize settling time and to maximize extraction of Ca and Mg for carbonation reactions during ore processing.
Journal of South American Earth Sciences, Vol. 70, pp. 162-173.
South America
Craton
Abstract: The Amazonian craton, which covers a large area of South America, and is thought to have been stable since the end of the Mesoproterozoic, has recently benefited from a series of regional geophysical surveys. The Amazonian craton comprises the northern Guyana shield and the southern Central Brazil shield. It has become the main subject of seismological studies aiming to determine crustal thickness. Moho thickness maps that cover a large part of the South American continent summarize these studies. Receiver function studies, aided by surface wave dispersion tomography, were also useful tools applied in the region over the past decade. These have been improved by the addition of temporary and permanent regional seismological arrays and stations. An interesting NNW-SSE Moho depth anomaly, pointing to crustal thickening of up to 60 km in the central Guyana shield and a 50 km thick anomaly of the southern Central Brazil shield were recently identified. Areas with crustal thickening correspond to Paleoproterozoic magmatic arcs. The upper mantle seismic anisotropy in part of the region has been determined from SKS splitting studies. The currently available seismic anisotropy information shows that the orientation of the determined anisotropic axis is related to the frozen in anisotropy hypothesis for the Amazonian craton. The orientation of the anisotropic axis shows no relation to the current South American plate motion in the Amazonian craton. Most recently, detailed information for the two shields has benefited from a series of high-resolution, regional aerogeophysical surveys, made available by CPRM, the Brazilian Geological Survey. In addition to the mentioned contribution from seismology for imaging deeper crustal structures, regional gravity surveys have been expanded, adding to previous Bouguer anomaly maps, and deep drilling information from early exploration efforts have been compiled for the Amazon basin, which covers the Amazonian craton separating the Guyana and Central Brazil shields.
Abstract: Chemical events involving deep carbon- and water-rich fluids impact the continental lithosphere over its history. Diamonds are a by-product of such episodic fluid infiltrations, and entrapment of these fluids as microinclusions in lithospheric diamonds provide unique opportunities to investigate their nature. However, until now, direct constraints on the timing of such events have not been available. Here we report three alteration events in the southwest Kaapvaal lithosphere using U-Th-He geochronology of fluid-bearing diamonds, and constrain the upper limit of He diffusivity (to D???1.8?×?10?19 cm2 s?1), thus providing a means to directly place both upper and lower age limits on these alteration episodes. The youngest, during the Cretaceous, involved highly saline fluids, indicating a relationship with late-Mesozoic kimberlite eruptions. Remnants of two preceding events, by a Paleozoic silicic fluid and a Proterozoic carbonatitic fluid, are also encapsulated in Kaapvaal diamonds and are likely coeval with major surface tectonic events (e.g. the Damara and Namaqua-Natal orogenies).
Geochimica et Cosmochinica Acta, Vol. 215, pp. 432-446.
Africa, Zimbabwe
craton
Abstract: Hafnium and oxygen isotopic compositions measured in-situ on U-Pb dated zircon from Archaean sedimentary successions belonging to the 2.9–2.8 Ga Belingwean/Bulawayan groups and previously undated Sebakwian Group are used to characterize the crustal evolution of the Zimbabwe Craton prior to 3.0 Ga. Microstructural and compositional criteria were used to minimize effects arising from Pb loss due to metamorphic overprinting and interaction with low-temperature fluids. 207Pb/206Pb age spectra (concordance >90%) reveal prominent peaks at 3.8, 3.6, 3.5, and 3.35 Ga, corresponding to documented geological events, both globally and within the Zimbabwe Craton. Zircon ?18O values from +4 to +10‰ point to both derivation from magmas in equilibrium with mantle oxygen and the incorporation of material that had previously interacted with water in near-surface environments. In ?Hf-time space, 3.8–3.6 Ga grains define an array consistent with reworking of a mafic reservoir (176Lu/177Hf ?0.015) that separated from chondritic mantle at ?3.9 Ga. Crustal domains formed after 3.6 Ga depict a more complex evolution, involving contribution from chondritic mantle sources and, to a lesser extent, reworking of pre-existing crust. Protracted remelting was not accompanied by significant mantle depletion prior to 3.35 Ga. This implies that early crust production in the Zimbabwe Craton did not cause complementary enriched and depleted reservoirs that were tapped by later magmas, possibly because the volume of crust extracted and stabilised was too small to influence (asthenospheric) mantle isotopic evolution. Growth of continental crust through pulsed emplacement of juvenile (chondritic mantle-derived) melts, into and onto the existing cratonic nucleus, however, involved formation of complementary depleted subcontinental lithospheric mantle since the early Archaean, indicative of strongly coupled evolutionary histories of both reservoirs, with limited evidence for recycling and lateral accretion of arc-related crustal blocks until 3.35 Ga.
Abstract: The present study contributes new constraints on, and definitions of, the reconstructed plate margins of India and Madagascar based on flexural isostasy along the Western Continental Margin of India (WCMI) and the Eastern Continental Margin of Madagascar (ECMM). We have estimated the nature of isostasy and crustal geometry along the two margins, and have examined their possible conjugate structure. Here we utilize elastic thickness (Te) and Moho depth data as the primary basis for the correlation of these passive margins. We employ the flexure inversion technique that operates in spatial domain in order to estimate the spatial variation of effective elastic thickness. Gravity inversion and flexure inversion techniques are used to estimate the configuration of the Moho/Crust-Mantle Interface that reveals regional correlations with the elastic thickness variations. These results correlate well with the continental and oceanic segments of the Indian and African plates. The present study has found a linear zone of anomalously low-Te (1-5 km) along the WCMI (~1680 km), which correlates well with the low-Te patterns obtained all along the ECMM. We suggest that the low-Te zones along the WCMI and ECMM represent paleo-rift inception points of lithosphere thermally and mechanically weakened by the combined effects of the Marion hotspot and lithospheric extension due to rifting. We have produced an India-Madagascar paleo-fit representing the initial phase of separation based on the Te estimates of the rifted conjugate margins, which is confirmed by a close-fit correlation of Moho geometry and bathymetry of the shelf margins. The matching of tectonic lineaments, lithologies and geochronological belts between India and Madagascar provide an additional support for the present plate reconstruction.
Abstract: The Kumta and Mercara suture zones welding together Archean crustal blocks in western peninsular India offer critical insights into Precambrian continental juxtapositions and the crustal evolution of eastern Gondwana. Here we present the results from an integrated study of the structure, geology, petrology, mineral chemistry, metamorphic P-T conditions, zircon U-Pb ages and Lu-Hf isotopes of metasedimentary rocks from the two sutures. The dominant rocks in the Kumta suture are greenschist- to amphibolite-facies quartz-phengite schist, garnet-biotite schist, chlorite schist, fuchsite schist and marble. The textural relations, mineral chemistry and thermodynamic modelling of garnet-biotite schist from the Kumta suture indicate peak metamorphic P-T conditions of ca. 11 kbar at 790 °C, with detrital SHRIMP U-Pb zircon ages ranging from 3420 to 2547 Ma, ?Hf (t) values from ? 9.2 to 5.6, and TDMc model ages from 3747 to 2792 Ma. The K-Ar age of phengite from quartz-phengite schist is ca. 1326 Ma and that of biotite from garnet-biotite schist is ca. 1385 Ma, which are interpreted to broadly constrain the timing of metamorphism related to the suturing event. The Mercara suture contains amphibolite- to granulite-facies mylonitic quartzo-feldspathic gneiss, garnet-kyanite-sillimanite gneiss, garnet-biotite-kyanite-gedrite-cordierite gneiss, garnet-biotite-hornblende gneiss, calc-silicate granulite and metagabbro. The textural relations, mineral chemistry and thermodynamic modelling of garnet-biotite-kyanite-gedrite-cordierite gneiss from the Mercara suture indicate peak metamorphic P-T conditions of ca. 13 kbar at 825 °C, followed by isothermal decompression and cooling. For pelitic gneisses from the Mercara suture, LA-ICP-MS U-Pb zircon ages vary from 3249 to 3045 Ma, ?Hf (t) values range from ? 18.9 to 4.2, and TDMc model ages vary from 4094 to 3314 Ma. The lower intercept age of detrital zircons in the pelitic gneisses from the Mercara suture ranges from 1464 to 1106 Ma, indicating the approximate timing of a major lead-loss event, possibly corresponding to metamorphism, and is broadly coeval with events in the Kumta suture. Synthesis of the above results indicates that the Kumta and Mercara suture zones incorporated sediments from Palaeoarchean to Mesoproterozoic sources and underwent high-pressure metamorphism in the late Mesoproterozoic. The protolith sediments were derived from regions containing juvenile Palaeoarchean crust, together with detritus from the recycling of older continental crust. Integration of the above results with published data suggests that the Mesoproterozoic (1460-1100 Ma) Kumta and Mercara suture zones separate the Archean (3400-2500 Ma) Karwar-Coorg block and Dharwar Craton in western peninsular India. Based on regional structural and other geological data we interpret the Kumta and Mercara suture zones as extensions of the Betsimisaraka suture of eastern Madagascar into western India.
High temperature, high pressure granulites ( retrogressed eclogites) in the central region of the Lewisian NW Scotland: crustal scale subduction in the Neoarchean.
Oliveira, E.P., Talavera, C., Windley, B.F., Zhao, L., Semprich, J.J., McNaughton, N.J., Amaral, W.S., Sombini, G., Navarro, M., Silva, D.
Mesoarchean ( 2820 Ma )high pressure mafic granulite at Uaus, Sao Francisco craton, Brazil, and its potential significance for the assembly of Archean supercraton.
Precambrian Research, in press available, 43p. Pdf
Mantle
plate tectonics
Abstract: One of the most contentious areas of Earth Science today is when, or whether or not modern-style plate tectonics was in operation in the Archean Eon. In this review we present evidence that the onset of plate tectonics was not at 3.2 Ga, as popularly conceived, but was in operation during the Eoarchean by at least ca. 4.0 Ga. Following a review of the main Eoarchean supracrustal belts of the world, constrained by relevant geochemical/isotopic data, we present evidence that suggests that from at least ca. 4.0 Ga Earth produced considerable juvenile mafic crust and consequent island arcs by Accretionary Cycle Plate Tectonics. From ~3.2 Ga there was a gradual transition in geodynamics to more abundant active continental margin magmatism in the form of voluminous TTGs and sanukitoids. From 3.2 Ga to 2.5 Ga juvenile oceanic crust and arcs continued to form, accompanied by more active continental margin magmatism until ~2.7-2.5 Ga, by which time there were sufficient crustal rocks to amalgamate into incipient large continents, the fragmentation of which started the first complete classical Wilson Cycle Plate Tectonics of breaking apart and re-assembling large continental masses. In other words, there were two types of plate tectonics in operation in the early Earth, Accretionary Cycle Plate Tectonics and Wilson Cycle Plate Tectonics, but Wilson Cycle type plate interactions only became more common after contiguous continental landmass became voluminous and extensive enough around 2.7-2.5 Ga. Failure to realize this dual mechanism of continental growth may lead to erroneous ideas such as "plate tectonics started at 3.2 Ga", or "mantle plumes generated early Archean magmatic rocks." We present new geochemical data that together with lithological and structural relationships, negate the various plume-type speculations including stagnant lids, heat pipes, and mushy-lid tectonics. It is interesting to consider that the way Earth’s crust developed in the first Gigayear of the geological record continued later, albeit in more advanced forms, into the Phanerozoic, where we can still recognize Accretionary Cycle Plate Tectonics and orogens still with short boundaries in examples including the Altaids of Central Asia, the Arabian-Nubian Shield, the Japanese Islands, and in incipient form in Indonesia, as well as Wilson Cycle Plate Tectonics that leads inexorably to continental collisions as in the Alpine-Himalayan orogen with its long plate boundaries. We recommend this holistic view of crustal growth and the evolution of continents that leads to a robust, viable, and testable model of Earth evolution.
Precambrian Research, doi.org/1-.1016/ j.precamres.2020 .105980, 43p. Pdf
Mantle
plate tectonics
Abstract: One of the most contentious areas of Earth Science today is when, or whether or not modern-style plate tectonics was in operation in the Archean Eon. In this review we present evidence that the onset of plate tectonics was not at 3.2 Ga, as popularly conceived, but was in operation during the Eoarchean by at least ca. 4.0 Ga. Following a review of the main Eoarchean supracrustal belts of the world, constrained by relevant geochemical/isotopic data, we present evidence that suggests that from at least ca. 4.0 Ga Earth produced considerable juvenile mafic crust and consequent island arcs by Accretionary Cycle Plate Tectonics. From ~3.2 Ga there was a gradual transition in geodynamics to more abundant active continental margin magmatism in the form of voluminous TTGs and sanukitoids. From 3.2 Ga to 2.5 Ga juvenile oceanic crust and arcs continued to form, accompanied by more active continental margin magmatism until ~2.7-2.5 Ga, by which time there were sufficient crustal rocks to amalgamate into incipient large continents, the fragmentation of which started the first complete classical Wilson Cycle Plate Tectonics of breaking apart and re-assembling large continental masses. In other words, there were two types of plate tectonics in operation in the early Earth, Accretionary Cycle Plate Tectonics and Wilson Cycle Plate Tectonics, but Wilson Cycle type plate interactions only became more common after contiguous continental landmass became voluminous and extensive enough around 2.7-2.5 Ga. Failure to realize this dual mechanism of continental growth may lead to erroneous ideas such as "plate tectonics started at 3.2 Ga", or "mantle plumes generated early Archean magmatic rocks." We present new geochemical data that together with lithological and structural relationships, negate the various plume-type speculations including stagnant lids, heat pipes, and mushy-lid tectonics. It is interesting to consider that the way Earth’s crust developed in the first Gigayear of the geological record continued later, albeit in more advanced forms, into the Phanerozoic, where we can still recognize Accretionary Cycle Plate Tectonics and orogens still with short boundaries in examples including the Altaids of Central Asia, the Arabian-Nubian Shield, the Japanese Islands, and in incipient form in Indonesia, as well as Wilson Cycle Plate Tectonics that leads inexorably to continental collisions as in the Alpine-Himalayan orogen with its long plate boundaries. We recommend this holistic view of crustal growth and the evolution of continents that leads to a robust, viable, and testable model of Earth evolution.
Abstract: The graphite-to-diamond transformation under shock compression has been of broad scientific interest since 1961. The formation of hexagonal diamond (HD) is of particular interest because it is expected to be harder than cubic diamond and due to its use in terrestrial sciences as a marker at meteorite impact sites. However, the formation of diamond having a fully hexagonal structure continues to be questioned and remains unresolved. Using real-time (nanosecond), in situ x-ray diffraction measurements, we show unequivocally that highly oriented pyrolytic graphite, shock-compressed along the c axis to 50 GPa, transforms to highly oriented elastically strained HD with the (100)HD plane parallel to the graphite basal plane. These findings contradict recent molecular dynamics simulation results for the shock-induced graphite-to-diamond transformation and provide a benchmark for future theoretical simulations. Additionally, our results show that an earlier report of HD forming only above 170 GPa for shocked pyrolytic graphite may lead to incorrect interpretations of meteorite impact events.
Cartigny, P., Farquar, J., Thomassot, E., Harris, J.W., Wing, B., Masterson, A., McKeegan, K., Stachel, T.
A mantle origin for Paleoarchean peridotite diamonds from the PAnd a kimberlite, Slave Province: evidence from 13C, 15N and 34,34S stable isotope systematics.
Abstract: The origin and evolution of Earth’s biosphere were shaped by the physical and chemical histories of the oceans. Marine chemical sediments and altered oceanic crust preserve a geochemical record of these histories. Marine chemical sediments, for example, exhibit an increase in their 18O/16O ratio through time. The implications of this signal are ambiguous but are typically cast in terms of two endmember (but not mutually exclusive) scenarios. The oceans may have been much warmer in the deep past if they had an oxygen isotope composition similar to that of today. Alternatively, the nature of fluid-rock interactions (including the weathering processes associated with continental emergence) may have been different in the past, leading to an evolving oceanic oxygen isotope composition. Here we examine approximately 3.24-billion-year-old hydrothermally altered oceanic crust from the Panorama district in the Pilbara Craton of Western Australia as an alternative oxygen isotope archive to marine chemical sediments. We find that, at that time, seawater at Panorama had an oxygen isotope composition enriched in 18O relative to the modern ocean with a ?18O of 3.3?±?0.1‰ VSMOW. We suggest that seawater ?18O may have decreased through time, in contrast to the large increases seen in marine chemical sediments. To explain this possibility, we construct an oxygen isotope exchange model of the geologic water cycle, which suggests that the initiation of continental weathering in the late Archaean, between 3 and 2.5 billion years ago, would have drawn down an 18O-enriched early Archaean ocean to ?18O values similar to those of modern seawater. We conclude that Earth’s water cycle may have gone through two separate phases of steady-state behaviour, before and after the emergence of the continents.
Journal of Metamorphic Geology, in press available
Mantle
Craton
Abstract: The Proterozoic belts that occur along the margins of the West Australian Craton, as well as those in intraplate settings, generally share similar geological histories that suggest a common plate-margin driver for orogeny. However, the thermal drivers for intraplate orogenesis are generally more poorly understood. The Mutherbukin Tectonic Event records a protracted period of Mesoproterozoic reworking of the Capricorn Orogen and offers significant insight into both the tectonic drivers and heat sources of long-lived intraplate orogens. Mineral assemblages and tectonic fabrics related to this event occur within a 50 km-wide fault-bound corridor in the central part of the Gascoyne Province in Western Australia. This zone preserves a crustal profile, with greenschist facies rocks in the north grading to upper amphibolite facies rocks in the south. The P- T-t evolution of 13 samples from 10 localities across the Mutherbukin Zone is investigated using phase equilibria modelling integrated with in situ U-Pb monazite and zircon geochronology. Garnet chemistry from selected samples is used to further refine the P-T history and shows that the dominant events recorded in this zone are prolonged D1 transpression between c. 1320 and 1270 Ma, followed by D2 transtension from c. 1210 to 1170 Ma. Peak metamorphic conditions in the mid-crust reached >650 °C and 4.4-7 kbar at c. 1210-1200 Ma. Most samples record a single clockwise P-T evolution during this event, although some samples might have experienced multiple perturbations. The heat source for metamorphism was primarily conductive heating of radiogenic mid- and upper crust, derived from earlier crustal differentiation events. This crust was thickened during D1 transpression, although the thermal effects persisted longer than the deformation event. Peak metamorphism was terminated by D2 transtension at c. 1210 Ma, with subsequent cooling driven by thinning of the radiogenic crust. The coincidence of a sedimentary basin acting as a thermal lid and a highly radiogenic mid-crustal batholith restricted to the Mutherbukin Zone accounts for reworking being confined to a discrete crustal corridor. Our results show that radiogenic regions in the shallow to mid crust can elevate the thermal gradient and localize deformation, causing the crust to be more responsive to far-field stresses. The Mutherbukin Tectonic Event in the Capricorn Orogen was synchronous with numerous Mesoproterozoic events around the West Australian Craton, suggesting that thick cratonic roots play an important role in propagating stresses generated at distant plate boundaries.
Journal of Metamorphic Geology, Vol. 35, 6, pp. 631-661.
Mantle
geothermometry
Abstract: The Proterozoic belts that occur along the margins of the West Australian Craton, as well as those in intraplate settings, generally share similar geological histories that suggest a common plate-margin driver for orogeny. However, the thermal drivers for intraplate orogenesis are more poorly understood. The Mutherbukin Tectonic Event records a protracted period of Mesoproterozoic reworking of the Capricorn Orogen and offers significant insight into both the tectonic drivers and heat sources of long-lived intraplate orogens. Mineral assemblages and tectonic fabrics related to this event occur within a 50 km-wide fault-bound corridor in the central part of the Gascoyne Province in Western Australia. This zone preserves a crustal profile, with greenschist facies rocks in the north grading to upper amphibolite facies rocks in the south. The P–T–t evolution of 13 samples from 10 localities across the Mutherbukin Zone is investigated using phase equilibria modelling integrated with in situ U–Pb monazite and zircon geochronology. Garnet chemistry from selected samples is used to further refine the P–T history and shows that the dominant events recorded in this zone are prolonged D1 transpression between c. 1,320 and 1,270 Ma, followed by D2 transtension from c. 1,210 to 1,170 Ma. Peak metamorphic conditions in the mid-crust reached >650°C and 4.4–7 kbar at c. 1,210–1,200 Ma. Most samples record a single clockwise P–T evolution during this event, although some samples might have experienced multiple perturbations. The heat source for metamorphism was primarily conductive heating of radiogenic mid- and upper crust, derived from earlier crustal differentiation events. This crust was thickened during D1 transpression, although the thermal effects persisted longer than the deformation event. Peak metamorphism was terminated by D2 transtension at c. 1,210 Ma, with subsequent cooling driven by thinning of the radiogenic crust. The coincidence of a sedimentary basin acting as a thermal lid and a highly radiogenic mid-crustal batholith restricted to the Mutherbukin Zone accounts for reworking being confined to a discrete crustal corridor. Our results show that radiogenic regions in the shallow to mid crust can elevate the thermal gradient and localize deformation, causing the crust to be more responsive to far-field stresses. The Mutherbukin Tectonic Event in the Capricorn Orogen was synchronous with numerous Mesoproterozoic events around the West Australian Craton, suggesting that thick cratonic roots play an important role in propagating stresses generated at distant plate boundaries.
Abstract: Impact cratering is a dynamic process that is violent and fast. Quantifying processes that accommodate deformation at different scales during central uplift formation in complex impact structures is therefore a challenging task. The ability to correlate mineral deformation at the microscale with macroscale processes provides a critical link in helping to constrain extreme crustal behavior during meteorite impact. Here we describe the first high-pressure-phase-calibrated chronology of shock progression in zircon from a central uplift. We report both shock twins and reidite, the high-pressure ZrSiO4 polymorph, in zircon from shocked granitic gneiss drilled from the center of the >60-km-diameter Woodleigh impact structure in Western Australia. The key observation is that in zircon grains that contain reidite, which forms at >30 GPa during the crater compression stage, the reidite domains are systematically offset by later-formed shock deformation twins (?20 GPa) along extensional planar microstructures. The {112} twins are interpreted to record crustal extension and uplift caused by the rarefaction wave during crater excavation. These results provide the first physical evidence that relates the formation sequence of both a high-pressure phase and a diagnostic shock microstructure in zircon to different cratering stages with unique stress regimes that are predicted by theoretical and numerical models. These microstructural observations thus provide new insight into central uplift formation, one of the least-understood processes during complex impact crater formation, which can produce many kilometers of vertically uplifted bedrock in seconds.
Jelsma, H.,Krishnan, S.U., Perritt, S.,Kumar, M., Preston, R., Winter, F., Lemotlo, L., Costa, J., Van der Linde, G., Facatino, M., Posser, A., Wallace, C., Henning, A., Joy, S., Chinn, I., Armstrong, R., Phillips, D.
Kimberlites from central Angola: a case stidy of exploration findings.
10th. International Kimberlite Conference Feb. 6-11, Bangalore India, Abstract
Jelsma, H., Krishnan, U., Perritt, S., Preston, R., Winter, F., Lemotlo, L., van der Linde, G., Armstrong, R., Phillips, D., Joy, S., Costa, J., Facatino, M., Posser, A., Kumar, M., Wallace, C., Chinn, I., Henning, A.
Kimberlites from central Angola: a case study of exploration findings.
Proceedings of the 10th. International Kimberlite Conference, Vol. 2, pp. 173-190.
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 193-198.
Technology
Rare earths
Abstract: Geochemical exploration for Nb, Ta, Zr and rare earth element (REE) mineralization associated with carbonatite, pegmatite, and peralkaline intrusions presents unique challenges and opportunities. The challenges are mainly due to the tendency of these elements, as High Field Strength Elements (HFSE), to be relatively immobile in surface environments in addition to commonly forming minerals that are resistant to weathering. In addition, many of the host minerals are resistant to routine exploration geochemistry digestions, which are typically aimed at dissolving soluble oxides or extracting more labile ionic forms (Reimann et al., 2014). Opportunities arise because host rocks typically represent relatively rare end products of the magmatic processes that generate peralkaline magmas including, at the far end of the spectrum, carbonatites. Hence host rocks are relatively easy to identify geochemically and commonly defi ne classic lithological zoning (e.g., Modreski et al., 1995). In addition, many of the minerals that contain these elements are resistant to weathering, mechanically durable, have relatively high densities, and have the have the potential to form heavy mineral concentrates when released by weathering. This is particularly so for Zr, Nb, and Ta, which form primary minerals such as tantalite (Ta Nb), pyrochlore (Nb), coltan (Ta Nb), columbianite (Ta Nb), dysanalite-perovskite (Nb) and zircon (Zr). In contrast, the REE are mobile in the weathering environment and commonly re-locate from primary carbonate and phosphate minerals (e.g., synchysite, monazite, xenotime, bastnäsite, allanite) to secondary phosphate minerals such as churchite (Lottermoser, 1990) and gorceixite (Mariano, 1989).
Abstract: Apatite-group phosphates are nearly ubiquitous in carbonatites, but our understanding of these minerals is inadequate, particularly in the areas of element partitioning and petrogenetic interpretation of their compositional variation among spatially associated rocks and within individual crystals. In the present work, the mode of occurrence, and major- and trace-element chemistry of apatite (sensu lato) from calcite and dolomite carbonatites, their associated cumulate rocks (including phoscorites) and hydrothermal parageneses were studied using a set of 80 samples from 50 localities worldwide. The majority of this set represents material for which no analytical data are available in the literature. Electron-microprobe and laser-ablation mass-spectrometry data (~ 600 and 400 analyses, respectively), accompanied by back-scattered-electron and cathodoluminescence images and Raman spectra, were used to identify the key compositional characteristics and zoning patterns of carbonatitic apatite. These data are placed in the context of phosphorus geochemistry in carbonatitic systems and carbonatite evolution, and compared to the models proposed by previous workers. The documented variations in apatite morphology and zoning represent a detailed record of a wide range of evolutionary processes, both magmatic and fluid-driven. The majority of igneous apatite from the examined rocks is Cl-poor fluorapatite or F-rich hydroxylapatite (? 0.3 apfu F) with 0.2-2.7 wt.% SrO, 0-4.5 wt.% LREE2O3, 0-0.8 wt.% Na2O, and low levels of other cations accommodated in the Ca site (up to 1000 ppm Mn, 2300 ppm Fe, 200 ppm Ba, 150 ppm Pb, 700 ppm Th and 150 ppm U), none of which show meaningful correlation with the host-rock type. Silicate, (SO4)2 ? and (VO4)3 ? anions, substituting for (PO4)3 ?, tend to occur in greater abundance in crystals from calcite carbonatites (up to 4.2 wt.% SiO2, 1.5 wt.% SO3 and 660 ppm V). Although (CO3)2 ? groups are very likely present in some samples, Raman micro-spectroscopy proved inconclusive for apatites with small P-site deficiencies and other substituent elements in this site. Indicator REE ratios sensitive to redox conditions (?Ce, ?Eu) and hydrothermal overprint (?Y) form a fairly tight cluster of values (0.8-1.3, 0.8-1.1 and 0.6-0.9, respectively) and may be used in combination with trace-element abundances for the development of geochemical exploration tools. Hydrothermal apatite forms in carbonatites as the product of replacement of primary apatite, or is deposited in fractures and interstices as euhedral crystals and aggregates associated with typical late-stage minerals (e.g., quartz and chlorite). Hydrothermal apatite is typically depleted in Sr, REE, Mn and Th, but enriched in F (up to 4.8 wt.%) relative to its igneous precursor, and also differs from the latter in at least some of key REE ratios [e.g., shows (La/Yb)cn ? 25, or a negative Ce anomaly]. The only significant exception is Sr(± REE,Na)-rich replacement zones and overgrowths on igneous apatite from some dolomite(-bearing) carbonatites. Their crystallization conditions and source fluid appear to be very different from the more common Sr-REE-depleted variety. Based on the new evidence presented in this work, trace-element partitioning between apatite and carbonatitic magmas, phosphate solubility in these magmas, and compositional variation of apatite-group minerals from spatially associated carbonatitic rocks are critically re-evaluated.
43rd Annual Yellowknife Geoscience Forum Abstracts, abstract p. 22.
Canada, Northwest Territories
Geochemistry
Abstract: Attention is being focused on the development of deep penetrating geochemical exploration methods as the discovery rate of world class deposits decreases. Diamondiferous kimberlites located in the Lac de Gras region of the Northwest Territories are one of the many deposit types in Canada covered by glacial overburden, and are therefore challenging to detect. This paper presents initial results from an investigation of the DO-18 kimberlite (Peregrine Diamonds), buried under 5-20m of glacial cover, to identify surface geochemical responses directly related to the buried kimberlite and differentiate between physical and chemical transport mechanisms. A detailed grid of 150 samples over an area of 0.5km2 sampled the oxidized upper B soil horizon in till above and off the DO-18 kimberlite into background. Regolith mapping was conducted and included surficial soil type and rock fragments, topographic variation and physical features, e.g. bogs, swamps, vegetation and glacial direction indicators. This allows an assessment of surface controls on the geochemistry, including the generation of false anomalies from chemical traps such as swamps. Multi-element geochemistry comprising 4-acid, Aqua-Regia and distilled water extraction coupled with ICP-MS was undertaken using commercial techniques to identify and differentiate between those elements migrating by chemical process from those migrating by physical transportation. Hydrocarbons were analysed using the SGH-technique (ActLabs) and the Gore-sorber technique (AGI) to characterize type and abundance of complex hydrocarbons above the kimberlite relative to the host granite gneiss. Preliminary results from the 4-acid digestion data show a clastic dispersion of Nb, Ni, Mg, Co, Cr and Cs from directly above the kimberlite to the edge of the sampling grid 500 metres northwest of the buried kimberlite. Surface material exhibits a strong control on geochemistry with trace elements being controlled by major elements (Al, Fe, Mn) found within each surface material type, and in some cases are heavily influenced by the presence of organic carbon. Evaluation of these relationships allows clarification of the natural background noise and enhancement of the geochemical responses and contrasts.
Direct discovery of concealed kimberlites with microbial community fingerprinting.
2018 Yellowknife Geoscience Forum , p. 36. abstract
Canada, Northwest Territories
mineral chemistry
Abstract: Mineral exploration in Canada is becoming increasingly complex as the majority of undiscovered commodities are likely deeply buried beneath significant glacial overburden and bedrock, reducing the effectiveness of many existing tools. The development of innovative exploration protocols and techniques is imperative to the continuation of discovery success. Preliminary experimentation has demonstrated the potential viability of microbial fingerprinting through genetic sequencing to directly identify the projected subcrop of mineralization in addition to the more distal entrained geochemical signatures in till. With the advent of inexpensive modern sequencing technology and big-data techniques, microbiological approaches to exploration are becoming more quantitative, cost effective, and efficient. The integration of microbial community information with soil chemistry, mineralogy and landscape development coupled with geology and geophysics propagates the development of an improved decision process in mineral exploration. Soils over porphyry, kimberlite, and VMS deposits have undergone microbial community profiling. These community-genome derived datasets have been integrated with trace metal chemistry, mineralogy, surface geology and other environmental variables including Eh and pH. Analyses of two kimberlites in the Northwest Territories show significant microbial community shifts that are correlated with subsurface mineralization, with distinctive microbial community profiles present directly above the kimberlite. The relationship between microbial profiles and mineralization leads to the use of microbial fingerprinting as a method for more accurately delineating ore deposits in glacially covered terrain. As databases are developed, there is potential for application as a field based technique, as sequencing technology is progressively developed into portable platforms.
Yellowknife Forum NWTgeoscience.ca, abstract volume p. 42-43.
Canada, Northwest Territories
kimberlite
Abstract: Mineral exploration in northern latitudes is challenging in that undiscovered deposits are likely buried beneath significant glacial overburden. The development of innovative exploration strategies and robust techniques to see through cover is imperative to future discovery success. Microbial communities are sensitive to subtle environmental fluctuations, reflecting these changes on very short timescales. Shifts in microbial community profiles, induced by chemical differences related to geology, are detectable in the surficial environment, and can be used to vector toward discrete geological features. The modernization of genetic sequencing and big-data evaluation allows for efficient and cost-effective microbial characterization of soil profiles, with the potential to see through glacial cover. Results to date have demonstrated the viability of microbial fingerprinting to directly identify the surface projection of kimberlites in addition to entrained geochemical signatures in till. Soils above two kimberlites in the Northwest Territories, have undergone microbial community profiling. These community-genome derived datasets have been integrated with chemistry, mineralogy, surface geology, vegetation type and other environmental variables including Eh and pH. Analyses show significant microbial community shifts, correlated with the presence of kimberlites, with a distinct community response at the species level directly over known deposits. Diversity of soil bacteria is also depressed in the same regions of the microbial community response. The relationship between microbial profiles and buried kimberlites has led to the application of microbial fingerprinting as a method to accurately delineate potential ore deposits in covered terrain. The integration of microbial community information with soil chemistry and landscape development coupled with geology and geophysics significantly improves the drill / no-drill decision process and has proven to be far more accurate than traditional surficial exploration methods. There is high potential for application as a field-based technique as microbial databases for kimberlites in northern regions are refined, and as sequencing technology is progressively developed into portable platforms.
Yellowknife Forum NWTgeoscience.ca, abstract volume poster p. 123-124.
Canada, Northwest Territories
deposit - Kelvin
Abstract: Research at the Kelvin kimberlite, NWT, is defining surface exploration practices and testing new host rock lithogeochemical exploration tools that will result in reduced costs and improved discovery success. In regions where recent glaciation has buried kimberlites under glacial sediments, surface geochemical detection methods are best interpreted when coupled with a comprehension of the landscape formation processes. The glacial, post-glacial, and cryoturbation processes that have affected the landscape have, in turn, affected the dispersal of geochemical signatures in the till that can be detected and exploited by detailed surface mapping, sampling, and geochemical analysis. The Kelvin kimberlite is an inclined pipe that subcrops from metaturbidite country rock beneath a lake. No indicator mineral train has been detected at Kelvin by traditional indicator mineral methods. Relative uniformity of surficial material (<6m thick till blanket) allows for extensive B horizon soil sampling above the kimberlite, up-ice, and up to 1 km down-ice. Four acid and aqua regia ICP-MS results of the -180 ?m fraction indicate the presence of subtle pathfinder element trains originating from the kimberlite subcrop location and extending for >1km down-ice. Dry sonic sieving and four acid digestion results provide interpretations of geochemical partitioning and the ideal size fraction for geochemical sampling. Trace elements demonstrate systematically elevated concentrations in the fine and very fine silt fractions; however, background is higher and anomalous to background contrast is not enhanced compared to bulk -180 ?m ratios. Elevated pathfinder concentrations in the fine to very fine sand fraction are attributed to fine kimberlite indicator minerals and their fragments, and display the best anomalous to background contrast ratio. Whole soil commercial Pb isotope analysis of select soils provide supplemental data to fingerprint the petrogenetic source of anomalous samples. Additional research is being carried out to detect alteration signatures in the country rock induced by the emplacement of the kimberlite. Lithogeochemical data from four drill holes aims to identify and quantify the metasomatic enrichment and depletion of elements sourced from the kimberlite, while hyperspectral imaging will aim to detect secondary mineralogy and subtle changes in mineral composition. This data will be used to generate mineralogical and geochemical vectors beneficial in near-miss situations when drilling kimberlites and defining diatreme geometries.
Aravanis, T., Chen, J., Fuechsle, M., Grujic, M., Johnston, P., Kok, Y., Magaraggia, R., Mann, A., Mann, L., McIntoshm S., Rheinberger, G., Saxey, D., Smalley, M., van Kann, F., Walker, G., Winterflood, J.
Abstract: The minerals exploration industry’s demand for a highly precise airborne gravity gradiometer has driven development of the VK1TM Airborne Gravity Gradiometer, a collaborative effort by Rio Tinto and the University of Western Australia. VK1TM aims to provide gravity gradient data with lower uncertainty and higher spatial resolution than current commercial systems. In the recent years of VK1TM development, there have been significant improvements in hardware, signal processing and data processing which have combined to result in a complete AGG system that is approaching competitive survey-ready status. This paper focuses on recent improvements. Milestone-achieving data from recent lab-based and moving-platform trials will be presented and discussed, along with details of some advanced data processing techniques that are required to make the most use of the data.
Till geochemistry and lithogeochemical exploration for a concealed kimberlite.
2018 Yellowknife Geoscience Forum , p. 88-89. abstract
Canada, Northwest Territories
deposit - Kelvin
Abstract: Research at the Kelvin kimberlite, NWT is defining surface exploration practices and developing new exploration tools based on host rock lithogeochemical alteration, that will result in reduced costs and improved discovery success. In regions where recent glaciation has buried kimberlites under glacial sediments, surface geochemical detection methods are best interpreted when coupled with a comprehension of the landscape formation processes. The glacial, post-glacial, and cryoturbation processes that have affected the landscape have, in turn, affected the dispersal of geochemical signatures in the till that can be detected and exploited by detailed surface mapping, sampling, and geochemical analysis. Additionally, the application of geochemical and hyperspectral data to country rock alteration core can aid in the detection of kimberlites during near-miss drilling campaigns. The Kelvin kimberlite is located eight kilometers from the Gahcho Kué diamond mine in the Northwest Territories. The inclined pipe sub-crops beneath a lake and dips into gneiss country rock towards the northwest with a surface projection of more than 600 m long. Relative uniformity of surficial material (<6 m thick till veneer) allows for extensive b-horizon soil sampling above the kimberlite, up-ice, and up to 1 km in the down-ice direction. Samples were sieved to -180 microns and analyzed by four acid digest ICP-MS and aqua-regia digest ICP-MS. Results indicate the soils to be very immature and identify the presence of a subtle Ni-Cr-Mg-Nb train originating from the lake side extending for >1km from source following the most recent ice direction to the west. The material for the train was abraded by the ice from the kimberlite, now sub-cropping beneath a lake, and would have provided additional support to drill what was initially targeted from geophysics. Additional research is being carried out to detect alteration signatures in the country rock induced by the emplacement of the kimberlite. Lithogeochemical data from four drill holes aims to identify and quantify the metasomatic enrichment and depletion of elements sourced from the kimberlite while accounting for country-rock lithology variation. Hyperspectral imaging of the same drill core will aim to detect and quantify secondary mineralogy and subtle changes in mineral composition that otherwise cannot be detected visually. This data will be used to generate mineralogical and chemical vectors beneficial in near-miss situations when drilling kimberlites and defining diatreme geometries.
Geochemistry, Geophysics, Geosystems G3, pp. 4326-
Mantle
geophysics
Abstract: Regional characterization of the continental crust has classically been performed through either geologic mapping, geochemical sampling, or geophysical surveys. Rarely are these techniques fully integrated, due to limits of data coverage, quality, and/or incompatible data sets. We combine geologic observations, geochemical sampling, and geophysical surveys to create a coherent 3-D geologic model of a 50 × 50 km upper crustal region surrounding the SNOLAB underground physics laboratory in Canada, which includes the Southern Province, the Superior Province, the Sudbury Structure, and the Grenville Front Tectonic Zone. Nine representative aggregate units of exposed lithologies are geologically characterized, geophysically constrained, and probed with 109 rock samples supported by compiled geochemical databases. A detailed study of the lognormal distributions of U and Th abundances and of their correlation permits a bivariate analysis for a robust treatment of the uncertainties. A downloadable 3-D numerical model of U and Th distribution defines an average heat production of math formula µW/m3, and predicts a contribution of math formula TNU (a Terrestrial Neutrino Unit is one geoneutrino event per 1032 target protons per year) out of a crustal geoneutrino signal of math formula TNU. The relatively high local crust geoneutrino signal together with its large variability strongly restrict the SNO+ capability of experimentally discriminating among BSE compositional models of the mantle. Future work to constrain the crustal heat production and the geoneutrino signal at SNO+ will be inefficient without more detailed geophysical characterization of the 3-D structure of the heterogeneous Huronian Supergroup, which contributes the largest uncertainty to the calculation.
Journal of Geophysical Research, Vol. 121, 9, pp. 6675-6697.
United States, Canada
Geophysics
Abstract: The observation of widespread seismic discontinuities within Archean and Proterozoic lithosphere is intriguing, as their presence may shed light on the formation and early evolution of cratons. A clear explanation for the discontinuities, which generally manifest as a sharp decrease in seismic velocity with depth, remains elusive. Recent work has suggested that midlithospheric discontinuities (MLDs) may correspond to a sharp gradient in seismic anisotropy, produced via deformation associated with craton formation. Here we test this hypothesis beneath the Archean Superior and Wyoming Provinces using anisotropic Ps receiver function (RF) analysis to characterize the relationship between MLDs and seismic anisotropy. We computed radial and transverse component RFs for 13 long-running seismic stations. Of these, six stations with particularly clear signals were analyzed using a harmonic regression technique. In agreement with previous studies, we find evidence for multiple MLDs within the cratonic lithosphere of the Wyoming and Superior Provinces. Our harmonic regression results reveal that (1) MLDs can be primarily explained by an isotropic negative velocity gradient, (2) multiple anisotropic boundaries exist within the lithospheric mantle, (3) the isotropic MLD and the anisotropic boundaries do not necessarily occur at the same depths, and (4) the depth and geometry of the anisotropic boundaries vary among stations. We infer that the MLD does not directly correspond to a change in anisotropy within the mantle lithosphere. Furthermore, our results reveal a surprising level of complexity within the cratonic lithospheric mantle, suggesting that the processes responsible for shaping surface geology produce similar structural complexity at depth.
Sobolev, N., Wirth, R., Logvinova, A.M., Pokhilenko, N.P., Kuzmin, D.V.
Retrograde phase transitions of majorite garnets included in diamonds: a case study of subcalcic Cr rich majorite pyrope from a Snap Lake diamond, Canada.
American Geological Union, Fall meeting Dec. 15-19, Eos Trans. Vol. 89, no. 53, meeting supplement, 1p. abstract
Konzett, J., Wirth, R., Hauzenberger, C., Whitehouse, M.
Two episodes of fluid migration in the Kaapvaal Craton lithospheric mantle associated with Cretaceous kimberlite activity: evidence from a harzburgite containing a unique assemblage of metasomatic zirconium-phases.
Logvinova, A., Wirth, R., Taylor, L.A., Sobolev, N.V.
Aragonite, magnesite and dolomite inclusions in Yakutian diamonds: TEM observations.
V.S. Sobolev Institute of Geology and Mineralogy Siberian Branch Russian Academy of Sciences International Symposium Advances in high pressure research: breaking scales and horizons ( Courtesy of N. Poikilenko), Held Sept. 22-26, 1p. Abstract
Shertl, H.P., Neuser, R.D., Logvinova, A.M., Wirth, R., Sobolev, N.V.
Cathodluminescence microscopy of the Kokchetav ultra high pressure calcsilicate rocks: what can we learn from silicates, carbon hosting minerals and diamond?
Russian Geology and Geophysics, Vol. 56, 1-2, pp. 100-112.
Contributions to Mineralogy and Petrology, Vol. 169, 19p.
Russia, Kazakhstan
Diamondiferous tourmaline
Abstract: Tourmaline was synthesized in the system MgO-Al2O3-B2O3-SiO2-KCl-NaCl-H2O from an oxide mixture and excess fluid at 500-700 °C and 0.2-4.0 GPa to investigate the effect of pressure, temperature, and fluid composition on the relative incorporation of Na and K in dravitic tourmaline. Incorporation of K at the X-site increases with pressure, temperature, and KCl concentration; a maximum of 0.71 K pfu (leaving 0.29 X-vacant sites pfu) was incorporated into K-dravite synthesized at 4.0 GPa, 700 °C from a 4.78 m KCl, Na-free fluid. In contrast, Na incorporation depends predominately on fluid composition, rather than pressure or temperature; dravite with the highest Na content of 1.00 Na pfu was synthesized at 0.4 GPa and 700 °C from a 3.87 m NaCl and 1.08 m KCl fluid. All synthesized crystals are zoned, and the dominant solid solution in the Na- and K-bearing system is between magnesio-foitite [?(Mg2Al)Al6Si6O18(BO3)3(OH)3OH] and dravite [NaMg3Al6Si6O18(BO3)3(OH)3(OH)], with the dravitic component increasing with the concentration of Na in the fluid. In the K-bearing, Na-free system, the dominant solid solution is between magnesio-foitite and K-dravite [KMg3Al6Si6O18(BO3)3(OH)3(OH)], with the K-dravitic component increasing with pressure, temperature, and the concentration of K in the fluid. The unit-cell volume of tourmaline increases with K incorporation from 1555.1(3) to 1588.1(2) Å3, reflecting the incorporation of the relatively large K+ ion. Comparison of our results to the compositional data for maruyamaite (K-dominant tourmaline) from the ultrahigh-pressure rocks of the Kokchetav Massif in Kazakhstan suggests that the latter was formed in a K-rich, Na-poor environment at ultrahigh-pressure conditions near the diamond-stability field.
Abstract: In recent years we have confirmed the existence of ophiolite-hosted diamonds on Earth, which occur in mantle peridotites and podiform chromitites of many ophiolites. These diamonds differ significantly from most kimberlite varieties, particularly in their inclusions. The typical inclusions in the diamonds are Mn-rich phases, i.e., NiMnCo alloy, native Mn, MnO, galaxite, Mn olivine and Mn garnet. Ca-silicate perovskite, a typical lower mantle mineral, was identified as mineral inclusions in diamond. One occurs as a 60-nanometer, euhedral grain associated with NiMnCo alloy and graphite, while another one occurs as a 50-nanometer grain within a large inclusion containing both NiMnCo alloy and Nd-Se-Cu-S phase. By EDS the perovskite has Ca 48.3%, Si 37.7% and Mn 14.1% with oxygen. TEM diffraction data show that the inclusion has d-spacings and angles between adjacent lattice planes are consistent to the Ca-silicate perovskite with an orthorhombic structure. The only known source of such light carbon is organic material in surface sediments and the best known sources of abundant manganese are Fe-Mn-rich sediments and Mn nodules, both of which are common on the seafloor. Many parts of the modern seafloor are also covered by sediments with a continental provenance. Phases such as SiO2 and Al2O3 are not expected in mantle peridotites and must have been introduced from shallow levels. We propose that subduction of oceanic lithosphere carries C, Mn, Si, Al and REE to the transition zone or lower mantle where the material is mixed with highly reduced material, perhaps derived from greater depths. Crystallization of diamond from a C-rich fluid encapsulates the observed inclusions. The diamonds and associated minerals are incorporated into chromite grains during chromite crystallization at depth of mantle transition zone, and are carried to shallower levels by mantle convection. Accumulation of chromite grains produces podiform chromitites containing a range of exotic minerals. However, the presence of diamonds and other UHP minerals in ophiolitic peridotites indicates that such phases can persist far outside their normal stability fields.
Mineralogy and Petrology, DOI 10. 1007/s00710-015-0401-7
South America, Brazil, Mato Grosso
Juina area
Abstract: Two carbonatitic mineral assemblages, calcite + wollastonite and calcite + monticellite, which are encapsulated in two diamond grains from the Rio Soriso basin in the Juina area, Mato Grosso State, Brazil, were studied utilizing the NanoSIMS technique. The assemblages were formed as the result of the decomposition of the lower-mantle assemblage calcite + CaSi-perovskite + volatile during the course of the diamond ascent under pressure conditions from 15 to less than 0.8 GPa. The oxygen and carbon isotopic compositions of the studied minerals are inhomogeneous. They fractionated during the process of the decomposition of primary minerals to very varying values: ?18O from ?3.3 to +15.4?‰SMOW and ?13C from ?2.8 to +9.3?VPDB. These values significantly extend the mantle values for these elements in both isotopically-light and isotopically-heavy areas.
Yang, J.S., Wirth, R., Wiedenbeck, M., Griffin, W.L., Meng, F.C., Chen, S.Y., Bai, W.J., Xu, X.X., Makeeyev, A.B., Bryanchaniniova, N.I.
Diamonds and highly reduced minerals from chromitite of the Ray-Iz ophiolite of the Polar Urals: deep origin of podiform chromitites and ophiolitic diamonds.
Mineralogy and Petrology, in press available, 12p.
South America, Brazil
Deposit - Juina
Abstract: In addition to ultramafic and mafic associations, a primary natrocarbonatitic association occurs in the lower mantle. To date, it was identified as inclusions in diamonds from the Juina area, Mato Grosso State, Brazil. It comprises almost 50 mineral species: carbonates, halides, fluorides, phosphates, sulfates, oxides, silicates, sulfides and native elements. In addition, volatiles are present in this association. Among oxides, coexisting periclase and wüstite were identified, pointing to the formation of the natrocarbonatitic association at a depth greater than 2000 km. Some iron-rich (Mg,Fe)O inclusions in diamond are attributed to the lowermost mantle. The initial lower-mantle carbonatitic melt formed as a result of low-fraction partial melting of carbon-containing lower-mantle material, rich in P, F, Cl and other volatile elements, at the core-mantle boundary. During ascent to the surface, the initial carbonatitic melt dissociated into two immiscible parts, a carbonate-silicate and a chloride-carbonate melt. The latter melt is parental to the natrocarbonatitic lower-mantle association. Diamonds with carbonatitic inclusions were formed in carbonatitic melts or high-density fluids.
Abstract: In addition to a series of finds of diamond in mafic volcanic and ultramafic massive rocks in Kamchatka, Russia, a carbonado-like diamond aggregate was identified in recent lavas of the active Avacha volcano. This aggregate differs from ‘classic carbonado’ by its location within an active volcanic arc, well-formed diamond crystallites, and cementing by Si-containing aggregates rather than sintering. The carbonado-like aggregate contains inclusions of Mn-Ni-Si-Fe alloys, native ?-Mn, tungsten and boron carbides, which are uncommon for both carbonado and monocrystalline diamonds. Mn-Ni-Si-Fe alloys, trigonal W2C and trigonal B4C are new mineral species that were not previously found in the natural environment. The formation of the carbonado-like diamond aggregate started with formation at ~ 850-1000 °C of tungsten and boron carbides, Mn-Ni-Si-Fe alloys and native ?-Mn, which were used as seeds for the subsequent crystallization of micro-sized diamond aggregate. In the final stage, the diamond aggregate was cemented by amorphous silica, tridymite, ?-SiC, and native silicon. The carbonado-like aggregate was most likely formed at near-atmospheric pressure conditions via the CVD mechanism during the course or shortly after one of the volcanic eruption pulses of the Avacha volcano. Volcanic gases played a great role in the formation of the carbonado-like aggregate.
Sverkhtverdie Materiali ( Ukraine) in RUSSIAN, No. 2, pp. 3-17.
Technology
Morphology of lonsdaleite, diamond
Abstract: External and internal morphologies of natural impact apographitic diamonds (paramorphoses) have been studied. The (0001) surface morphology of the paramorphoses reflects their phase composition and the structural relationship of its constituting phases. Growth and etch figures together with the elements of crystal symmetry of lonsdaleite and diamond are developed on these surfaces. The crystal size of lonsdaleite is up to 100 nm, and that of diamond is up to 300 nm. Two types of structural relations between graphite, lonsdaleite, and diamond in the paramorphoses are observed: the first type (black, black-gray, colorless and yellowish paramorphoses): the (0001) graphite face is parallel to the (100) lonsdaleite face and parallel to (111) diamond; the second type (milky-white paramorphoses): the (0001) graphite is parallel to the (100) lonsdaleite and parallel to the (112) diamond. The first type of the paramorphoses contains lonsdaleite, diamond, graphite or diamond, lonsdaleite, the second type of the paramorphoses contains predominantly diamond. The direct phase transition of graphite ? lonsdaleite and/or graphite ?diamond occurred in the paramorphoses of the first type. A successive phase transition graphite ? lonsdaleite ? diamond was observed in the paramorphoses of the second type. The structure of the paramorphoses of this type shows characteristic features of recrystallization.
Abstract: Homogeneity of a peridotitic garnet inclusion in diamond demonstrating excess in Si concentration (i.e. presence of majorite component) was investigated by TEM using FIB prepared foils. The host diamond is a low-nitrogen brown stone, which can be related to type IIa with features of strong plastic deformation. The studied sample is represented by Ca-poor Cr-pyrope of harzburgitic (H) paragenesis from Snap Lake dyke, Canada The garnet had been previously reported to contain Si = 3.16 apfu. The revised examination of the sample, resulted in detection of extremely fine-grained symplectite consisting of low Ca-orthopyroxene, clinopyroxene, Cr-spinel and coesite completely located and isolated in the inner part of the garnet crystal, which forms a sharp interface with the surrounding homogeneous garnet. XRD study confirmed the presence of the minerals constituting the symplectite. EPMA showed an identical bulk chemistry of the nanometer-sized symplectite and garnet. Further polishing of the garnet inclusion on the same surface with diamond removed the symplectite, which possibly was present as a thin lens within garnet. The remaining garnet is completely homogeneous as checked by two profiles, and contains unusually high Ni (118.2 ppm) and depleted REE patterns. Estimated PT formation conditions of this garnet are 10.8 GPa and 1450 °C within asthenosphere. Symplectite testifies partial retrograde isochemical phase transformation of the examined garnet which is suggested to be caused by decompression along with plastic deformation of diamond within the coesite stability field at T > 1000 °C and depth no less than 100 km. Because previously published studies of rare majoritic garnets composition were performed by EPMA only, it is possible that the traces of partial phase transformation (symplectite formation) could have been overlooked without additional XRD and/or TEM/AEM studies.
Abstract: Abstract
In addition to a series of finds of diamond in mafic volcanic and ultramafic massive rocks in Kamchatka, Russia, a carbonado-like diamond aggregate was identified in recent lavas of the active Avacha volcano. This aggregate differs from ‘classic carbonado’ by its location within an active volcanic arc, well-formed diamond crystallites, and cementing by Si-containing aggregates rather than sintering. The carbonado-like aggregate contains inclusions of Mn-Ni-Si-Fe alloys, native ?-Mn, tungsten and boron carbides, which are uncommon for both carbonado and monocrystalline diamonds. Mn-Ni-Si-Fe alloys, trigonal W2C and trigonal B4C are new mineral species that were not previously found in the natural environment. The formation of the carbonado-like diamond aggregate started with formation at ~ 850-1000 °C of tungsten and boron carbides, Mn-Ni-Si-Fe alloys and native ?-Mn, which were used as seeds for the subsequent crystallization of micro-sized diamond aggregate. In the final stage, the diamond aggregate was cemented by amorphous silica, tridymite, ?-SiC, and native silicon. The carbonado-like aggregate was most likely formed at near-atmospheric pressure conditions via the CVD mechanism during the course or shortly after one of the volcanic eruption pulses of the Avacha volcano. Volcanic gases played a great role in the formation of the carbonado-like aggregate.
Geophysical Research Abstracts, Vol. 19, EGRU2017-1751, April 1p.
Mantle
Diamond, inclusions, nitrogen
Abstract: A few years ago a series of iron carbides Fe3C, Fe2C, Fe7C3 and Fe23C6 (haxonite) containing up to 7.3-9.1 at.% N (N/(N+C) = 0.19-0.27) was identi?ed as inclusions in diamonds from the Juina area, Brazil in association with native iron and graphite (Kaminsky and Wirth, 2011). Subsequently nitrocarbides and carbonitrides Fe3(C,N) and Fe9(C,N)4 (nitroyarlongite) containing 12.8-18.42 at.% N (N/(N+C) = 0.37-0.60) were identi?ed in a lower-mantle microxenolith in association with ferropericlase and two post-spinel oxides Mg-Cr-Fe-O (CT phase; Mg-xieite) and Ca-Cr-O (new mineral) with an orthorhombic structure (Kaminsky et al., 2015). Recently pure nitrides Fe3N with a trigonal structure P312 and Fe2N with an orthorhombic structure Pbcn were identi?ed among mineral inclusions from diamonds in the same area. They have admixtures of Cr (0.68-1.8 at.%), Ni (0.35-0.93 at.%) and Mn (0-1.22 at.%). Fe2N contains also an admixture of 5.1-7.6 at.% Si. The nitrides associate with nitroyarlongite Fe9(N0.8C0.2)4 and iron carbide Fe7C3, which contain nanocrystals of moissanite, hexagonal 6H polytype of SiC. Fe7C3 crystallizes, in the Fe-C system, the ?rst in association with diamond at pressures starting from 130 GPa, i.e. within the lowermost mantle, the D[U+02BA] layer. Native iron and a series of nitride-carbonitride-nitrocarbide-carbides associated with Fe7C3 form as a result of in?ltration of the Fe-Ni melt from the outer core into the lowermost mantle. This melt contains up to 10 % light elements, such as C, N, O and Si, which may be the source of nitrides-carbides. The existence of nitrides in the lower mantle helps to solve the problem of ‘missing nitrogen’ in the Earth’s nitrogen balance and consider the Earth’s core as the major reservoir of nitrogen. According to calculations, the total amount of nitrogen in the Earth’s core is 9,705 ×1021 grams, and in the mantle ?500 ×1021 grams (95 % and 4.5 % of the total amount of nitrogen respectively). In such a case the average concentration of nitrogen in the Earth is ?1,710 ppm, which is similar to the concentration of nitrogen in chondrites.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 1751 Abstract
Mantle
Diamond inclusions
Abstract: A few years ago a series of iron carbides Fe3C, Fe2C, Fe7C3 and Fe23C6 (haxonite) containing up to 7.3-9.1 at.% N (N/(N+C) = 0.19-0.27) was identified as inclusions in diamonds from the Juina area, Brazil in association with native iron and graphite (Kaminsky and Wirth, 2011). Subsequently nitrocarbides and carbonitrides Fe3(C,N) and Fe9(C,N)4 (nitroyarlongite) containing 12.8-18.42 at.% N (N/(N+C) = 0.37-0.60) were identified in a lower-mantle microxenolith in association with ferropericlase and two post-spinel oxides Mg-Cr-Fe-O (CT phase; Mg-xieite) and Ca-Cr-O (new mineral) with an orthorhombic structure (Kaminsky et al., 2015). Recently pure nitrides Fe3N with a trigonal structure P312 and Fe2N with an orthorhombic structure Pbcn were identified among mineral inclusions from diamonds in the same area. They have admixtures of Cr (0.68-1.8 at.%), Ni (0.35-0.93 at.%) and Mn (0-1.22 at.%). Fe2N contains also an admixture of 5.1-7.6 at.% Si. The nitrides associate with nitroyarlongite Fe9(N0.8C0.2)4 and iron carbide Fe7C3, which contain nanocrystals of moissanite, hexagonal 6H polytype of SiC. Fe7C3 crystallizes, in the Fe-C system, the first in association with diamond at pressures starting from 130 GPa, i.e., within the lowermost mantle, the D? layer. Native iron and a series of nitride-carbonitride-nitrocarbide-carbides associated with Fe7C3 form as a result of infiltration of the Fe-Ni melt from the outer core into the lowermost mantle. This melt contains up to 10 % light elements, such as C, N, O and Si, which may be the source of nitrides-carbides. The existence of nitrides in the lower mantle helps to solve the problem of 'missing nitrogen' in the Earth's nitrogen balance and consider the Earth's core as the major reservoir of nitrogen. According to calculations, the total amount of nitrogen in the Earth's core is 9,705 × 1021 grams, and in the mantle 500 × 1021 grams (95 % and 4.5 % of the total amount of nitrogen respectively). In such a case the average concentration of nitrogen in the Earth is 1,710 ppm, which is similar to the concentration of nitrogen in chondrites. References 1. Kaminsky, F. V., Wirth, R. (2011) Iron carbide inclusions in lower-mantle diamond from Juina, Brazil. Canadian Mineralogist 49(2), 555-572. 2. Kaminsky, F. V., Wirth, R., Schreiber, A. (2015) A microinclusion of lower-mantle rock and some other lower-mantle inclusions in diamond.
Abstract: The first finds of iron nitrides and carbonitride as inclusions in lower-mantle diamond from Rio Soriso, Brazil, are herein reported. These grains were identified and studied with the use of transmission electron microscopy (TEM), electron diffraction analysis (EDX), and electron energy loss spectra (EELS). Among nitrides, trigonal Fe3N and orthorhombic Fe2N are present. Carbonitride is trigonal Fe9(N0.8C0.2)4. These mineral phases associate with iron carbide, Fe7C3, silicon carbide, SiC, Cr-Mn-Fe and Mn-Fe oxides; the latter may be termed Mn-rich xieite. Our identified finds demonstrate a wide field of natural compositions from pure carbide to pure nitride, with multiple stoichiometries from M5(C,N)3 to M23(C,N)6 and with M/(C,N) from 1.65 to 3.98. We conclude that the studied iron nitrides and carbonitrides were formed in the lowermost mantle as the result of the infiltration of liquid metal, containing light elements from the outer core into the D? layer, with the formation of the association: native Fe0 + iron nitrides, carbides, and transitional compounds + silicon carbide. They indicated that major reservoirs of nitrogen should be expected in the core and in the lowermost mantle, providing some solution to the problem of nitrogen balance in the Earth
Abstract: Exhumed ultrahigh-pressure (UHP) terranes, involving slices of deeply subducted crustal rocks, provide unique material for studying material transfer in subduction zones. Diamond-bearing UHP rocks with sedimentary protoliths allow for tracing melting processes at both UHP and UHT including carbon cycling in the Earth. We studied microdiamonds and associated phases in two contrasting lithologies, (1) acid, quartzofeldpathic UHP gneiss composed of garnet, kyanite, feldspar, quartz and biotite, with a high ASI characteristic of sedimentary rocks, and (2) intermediate garnet-clinopyroxene rock containing quartz, feldspar, minor kyanite and biotite, which is metaluminous. Whereas rock (1) contains exclusively single octahedral diamonds with perfect crystal shape in garnet, kyanite (more common) and zircon, the microdiamonds in the rock (2) occur mostly as clusters of cuboid shape in garnet and zircon. Micro-Raman and FIB TEM data document presence of graphite, quartz and rutile at diamond/host interface or in separate multiple solid inclusions (MSI) whereas carbonates are practically absent. The morphology and lack of inclusions reflect relatively slow growth of the octahedral diamonds (rock 1) at lower fluid supersaturation. Individual deep and symmetrical negative trigons (AFM) on the (111) plane suggest dissolution by a residual silicate-carbonate melt. In contrast, polycrystallline character of diamond cuboids (rock 2) along with their common dissolution and formation of numerous tetragonal etch pits reflect relatively rapid growth of these grains from highly supersaturated fluid/melt. Peak P-T conditions for the UHP rocks of ? 1100ºC at 4.5 GPa are located above the phengite dehydration melting curve, where silicate melts are produced and may coexist with carbonate melts. In view of the light carbon isotope composition and lack of carbonates, we suggest that the diamonds crystallized from the graphitized primordial organic matter under reducing conditions at presence of silicate melt.
Abstract: Is there the existence of a water-rich zone in the mantle, currently one of the most discussed problem in mantle petrology? There are recent studies of low-water content in nominally anhydrous minerals in diamonds [1] and the chemistry of exceptionally rare phlogopite inclusions coexisting with peridotitic and eclogitic minerals in kimberlite-hosted diamonds [2]. Previous studies have shown that some rapidly formed diamonds reflect the composition of the environment in which they formed [3]. The minerals trapped during nucleation stage remain shielded from any changing conditions during further diamond growth or later mantle metasomatism. Thus, the analysis of diamond microinclusions is a major tool for the direct study of mantle high-density fluids (HDFs) from which the diamonds have precipitated [4]. Using transmission electron microscopy (TEM) techniques, we have investigated hydrous silicates inside nanometerscale, polyphased unclusions, especially in dark cloudy alluvial and kimberlite diamonds. Clinohumite, phlogopite, and phengite were detected. Hydrous silicate phases are accompanied by Ba-Sr-Ca -Fe-Mg carbonates, in addition to sulfides, oxides (magnetite, rutile, ilmenite), F-apatite, KCl, graphite, and fluid bubbles. A contrast occurs between clinohumite associated with phlogopite, F-apatite and highMg carbonates, but phengite, accompanied by a Al, Kbearing, unidentified silicate. These inclusions reflect the composition of fluid from which the host diamond crystallized. The mica composition, in most cases, has excess Si, similar to the high-silica mica identified within diamond microinclusions from Diavik [5]. The fluid-bearing carbonatitic-silicic diamonds grew in water-rich environments with extremely high K-activity, compared to most diamonds, which grew only within limited zones in the Earth’s mantle.
Proceedings of XXXIV held Aug. 4-9. Perchuk International School of Earth Sciences, At Miass, Russia, 2p. Abstract
Mantle
nitrogen
Abstract: The first finds of iron nitrides and carbonitride as inclusions in lower-mantle diamond from Rio Soriso, Brazil, are herein reported. These grains were identified and studied with the use of transmission electron microscopy (TEM), electron diffraction analysis (EDX), and electron energy loss spectra (EELS). Among nitrides, trigonal Fe3N and orthorhombic Fe2N are present. Carbonitride is trigonal Fe9(N0.8C0.2)4. These mineral phases associate with iron carbide, Fe7C3, silicon carbide, SiC, Cr-Mn-Fe and Mn-Fe oxides; the latter may be termed Mn-rich xieite. Our identified finds demonstrate a wide field of natural compositions from pure carbide to pure nitride, with multiple stoichiometries from M5(C,N)3 to M23(C,N)6 and with M/(C,N) from 1.65 to 3.98. We conclude that the studied iron nitrides and carbonitrides were formed in the lowermost mantle as the result of the infiltration of liquid metal, containing light elements from the outer core into the D? layer, with the formation of the association: native Fe? + iron nitrides, carbides, and transitional compounds + silicon carbide. They indicated that major reservoirs of nitrogen should be expected in the core and in the lowermost mantle, providing some solution to the problem of nitrogen balance in the Earth.
Abstract: Platelets in diamond are extended planar defects that are thought to be generated during the nitrogen aggregation process in type Ia diamonds. They were subjected to intensive research during the 1980s and 1990s but the techniques used for observation of defects in diamond have improved since that time and new insights can be gained by further study. This study combines high resolution Fourier Transform Infrared (FTIR) analysis, with an emphasis on the main platelet peak, and transmission electron microscopic (TEM) imaging. By performing TEM and FTIR analyses on volumes of diamond that were closely spatially related it is shown that the average platelet diameter, D, follows the relationship D=ax?b where x is the position of the platelet peak in the infrared spectrum, a is a constant and b is the minimum position of the platelet peak. The best fit to the data is obtained if a value of b=1360cm?1 is used, giving a fitted value of a=221. The observed variation in infrared (IR) peak width can also be explained in terms of this relationship. Additionally, platelet morphology was found to vary according to diameter with large platelets being more elongated. The tendency to become more elongated can be described by the empirical equation AR=11.9D+19.6+0.4 where AR is the aspect ratio. Using the relationships established here, it will be possible to study platelet abundance and size as a function of parameters such as nitrogen concentration, nitrogen aggregation and diamond residence time in the mantle. This work therefore will open up new methods for constraining the geological history of diamonds of different parageneses and from different localities.
Abstract: Here, we present studies of natural SiC that occurs in situ in tuff related to the Miocene alkaline basalt formation deposited in northern part of Israel. Raman spectroscopy, SEM and FIB-assisted TEM studies revealed that SiC is primarily hexagonal polytypes 4H-SiC and 6H-SiC, and that the 4H-SiC polytype is the predominant phase. Both SiC polytypes contain crystalline inclusions of silicon (Sio) and inclusions of metal-silicide with varying compositions (e.g. Si58V25Ti12Cr3Fe2, Si41Fe24Ti20Ni7V5Zr3, and Si43Fe40Ni17). The silicides crystal structure parameters match Si2TiV5 (Pm-3 m space group, cubic), FeSi2Ti (Pbam space group, orthorhombic), and FeSi2 (Cmca space group, orthorhombic) respectively. We hypothesize that SiC was formed in a local ultra-reduced environment at respectively shallow depths (60-100 km), through a "desilification" reaction of SiO2 with highly reducing fluids (H2O-CH4-H2-C2H6) arisen from the mantle "hot spot" and passing through alkaline basalt magma reservoir. SiO2 (melt) interacting with the fluids may originate from the walls of the crustal rocks surrounding this magmatic reservoir. The "desilification" process led to the formation of SiC and the reduction of metal-oxides to native metals, alloys, and silicides. The latter were trapped by SiC during its growth. Hence, interplate "hot spot" alkali basalt volcanism can now be included as a geological environment where SiC, silicon, and silicides can be found.
Abstract: In addition to a series of finds of diamond in mafic volcanic and ultramafic massive rocks in Kamchatka, Russia, a carbonado-like diamond aggregate was identified in recent lavas of the active Avacha volcano. This aggregate differs from 'classic carbonado' by its location within an active volcanic arc, well-formed diamond crystallites, and cementing by Si-containing aggregates rather than sintering. The carbonado-like aggregate contains inclusions of Mn-Ni-Si-Fe alloys, native ?-Mn, tungsten and boron carbides, which are uncommon for both carbonado and monocrystalline diamonds. Mn-Ni-Si-Fe alloys, trigonal W2C and trigonal B4C are new mineral species that were not previously found in the natural environment. The formation of the carbonado-like diamond aggregate started with formation at 850-1000 °C of tungsten and boron carbides, Mn-Ni-Si-Fe alloys and native ?-Mn, which were used as seeds for the subsequent crystallization of micro-sized diamond aggregate. In the final stage, the diamond aggregate was cemented by amorphous silica, tridymite, ?-SiC, and native silicon. The carbonado-like aggregate was most likely formed at near-atmospheric pressure conditions via the CVD mechanism during the course or shortly after one of the volcanic eruption pulses of the Avacha volcano. Volcanic gases played a great role in the formation of the carbonado-like aggregate.
Abstract: A series of polycrystalline diamond grains were found within the Valizhgen Peninsula in Koryakia, northern Kamchatka, Russia. A grain from the Aynyn River area is studied in detail with TEM. Diamond crystallites, 2-40 ?m in size are twinned and have high dislocation density. They are cemented with tilleyite Ca5(Si2O7)(CO3)2, SiC, Fe-Ni-Mn-Cr silicides, native silicon, graphite, calcite, and amorphous material. Among SiC grains, three polymorphs were discriminated: hexagonal 4H and 6H and cubic C3 (?-SiC). Silicides have variable stoichiometry with (Fe,Ni,Mn,Cr)/Si = 0.505-1.925. Native silicon is an open-framework allotrope of silicon S24, which has been observed, to date, as a synthetic phase only; this is a new natural mineral phase. Three types of amorphous material were distinguished: a Ca-Si-C-O material, similar in composition to tilleyite; amorphous carbon in contact with diamond, which includes particles of crystalline graphite; and amorphous SiO2. No regularity in the distribution of the amorphous material was observed. In the studied aggregate, diamond crystallites and moissanite are intensively twinned, which is characteristic for these minerals formed by gas phase condensation or chemical vapor deposition (CVD) processes. The synthetic analogs of all other cementing compounds (?-SiC, silicides, and native silicon) are typical products of CVD processes. This confirms the earlier suggested CVD mechanism for the formation of Avacha diamond aggregates. Both Avacha and Aynyn diamond aggregates are related not to "classic" diamond locations within stable cratons, but to areas of active and Holocene volcanic belts. The studied diamond aggregates from Aynyn and Avacha, by their mineralogical features and by their origin during the course of volcanic eruptions via a gas phase condensation or CVD mechanism, may be considered a new variety of polycrystalline diamond and may be called "kamchatite". Kamchatite extends the number of unusual diamond localities. It increases the potential sources of diamond and indicates the polygenetic character of diamond.
Abstract: Geophysical investigations and laboratory experiments provide strong evidence for subduction of ancient oceanic crust, and geological and mineralogical observations suggest that subducted oceanic crust is recycled into the upper mantle. This model is supported by some direct petrologic and miner-alogical evidence, principally the recovery of super-deep diamonds from kimberlites and the presence of crustal materials in ophiolitic chromitites and peridotites, but many details are still unclear. Here we report the discovery of ophiolite-hosted diamonds in the podiform chromitites of the Skenderbeu massif of the Mirdita ophiolite in the western part of Neo-Tethys. The diamonds are characterized by exceedingly light C isotopes (?13CPDB ~ -25‰), which we interpret as evidence for subduction of organic carbon from Earth's surface. They are also characterized by an exceptionally large range in ? 15Nair (-12.9‰ to +25.5‰), accompanied by a low N aggregation state. Materials sparsely included in diamonds include amorphous material, Ni-Mn-Co alloy, nanocrystals (20 × 20 nm) of calcium silicate with an orthorhombic perovskite structure (Ca-Pv), and fluids. The fluids coexisting with the alloy and Ca-Pv provide clear evidence that the diamonds are natural rather than synthetic. We suggest that the Skenderbeu diamonds nucleated and grew from a C-saturated, NiMnCo-rich melt derived from a subducted slab of ocean crust and lithosphere in the deep mantle, at least in the diamond stability field, perhaps near the top of the mantle transition zone. The subsequent rapid upward transport in channeled networks related to slab rollback during subduction initiation may explain the formation and preservation of Skenderbeu diamonds. The discovery of diamonds from the Mirdita ophiolite not only provides new evidence of diamonds in these settings but also provides a valuable opportunity to understand deep cycling of subducted oceanic crust and mantle composition.
Abstract: Monocrystalline type Ia diamonds with octahedral growth morphology prevail among lithospheric diamonds, including precious stones. Unlike less common ‘fibrous’ diamonds that grew from alkali-rich carbonate-bearing melts and fluids, the growth medium of ‘monocrystalline’ type Ia diamonds remains debatable. Here we report the first finding of an optically visible (~30??m in size) carbonate inclusion in the center of a gem type Ia octahedral diamond from the Sytykanskaya kimberlite pipe, Yakutia. We found that the inclusion consists of submicron size carbonate phases represented by K2Ca(CO3)2 bütschliite (~15?vol%), Na2Mg(CO3)2 eitelite (~5?vol%), and dolomite (~80?vol%). Although neither bütschliite nor eitelite can coexist with dolomite under mantle P-T conditions, these phases readily appear all together in the quenched products of carbonatite melt under mantle pressures. Thus, at the moment of capture, the inclusion material was a carbonatite melt with the following composition 10(K0.75Na0.25)2CO3?90(Ca0.57Mg0.43)CO3. The content of alkali carbonates at the level of 10?mol% indicates that the melt was formed at a temperature of ?1300?°C. The high K/Na and Ca/(Ca?+?Mg) ratios in this melt indicate its derivation by partial melting of recycled marine sediments (pelites). Considering an age of the last subduction event beneath the Siberian craton, our new finding implies that subducting slabs drag carbonated material of the continental crust beneath ancient cratons, where it experiences partial melting to form a potassic dolomitic melt responsible for the formation of most diamonds, since the Late Archean.
Abstract: The microinclusions in cuboid diamonds from Ebelyakh River deposits (northeastern Siberian craton) have been investigated by FIB/TEM techniques. It was found that these microinclusions have multiphase associations, containing silicates, oxides, carbonates, halides, sulfides, graphite, and fluid phases. The bulk chemical composition of the microinclusions indicates two contrasting growth media: Mg-rich carbonatitic and Al-rich silicic. Each media has their own specific set of daughter phases. Carbonatitic microinclusions are characterized by the presence of dolomite, phlogopite, apatite, Mg, Fe-oxide, KCl, rutile, magnetite, Fe-sulfides, and hydrous fluid phases. Silicic microinclusions are composed mainly of free SiO2 phase (quartz), high-Si mica (phengite), Al-silicate (paragonite), F-apatite, Ca-carbonates enriched with Sr and Ba, Fe-sulfides, and hydrous fluid phases. These associations resulted from the cooling of diamond-forming carbonatitic and silicic fluids/melts preserved in microinclusions in cuboid diamonds during their ascent to the surface. The observed compositional variations indicate different origins and evolutions of these fluids/melts.
Abstract: Monocrystalline type Ia diamonds with octahedral growth morphology prevail among lithospheric diamonds, including precious stones. Unlike less common ‘fibrous’ diamonds that grew from alkali-rich carbonate-bearing melts and fluids, the growth medium of ‘monocrystalline’ type Ia diamonds remains debatable. Here we report the first finding of an optically visible (~30??m in size) carbonate inclusion in the center of a gem type Ia octahedral diamond from the Sytykanskaya kimberlite pipe, Yakutia. We found that the inclusion consists of submicron size carbonate phases represented by K2Ca(CO3)2 bütschliite (~15?vol%), Na2Mg(CO3)2 eitelite (~5?vol%), and dolomite (~80?vol%). Although neither bütschliite nor eitelite can coexist with dolomite under mantle P-T conditions, these phases readily appear all together in the quenched products of carbonatite melt under mantle pressures. Thus, at the moment of capture, the inclusion material was a carbonatite melt with the following composition 10(K0.75Na0.25)2CO3?90(Ca0.57Mg0.43)CO3. The content of alkali carbonates at the level of 10?mol% indicates that the melt was formed at a temperature of ?1300?°C. The high K/Na and Ca/(Ca?+?Mg) ratios in this melt indicate its derivation by partial melting of recycled marine sediments (pelites). Considering an age of the last subduction event beneath the Siberian craton, our new finding implies that subducting slabs drag carbonated material of the continental crust beneath ancient cratons, where it experiences partial melting to form a potassic dolomitic melt responsible for the formation of most diamonds, since the Late Archean.
Abstract: Diamonds of eclogitic paragenesis are dominant in the placer deposits in the northeastern part of the Siberian Craton. Multiple inclusions and host diamonds carbon isotopes composition are consistent with a mixing model in which they result from the interaction of slab-derived melt/fluid with surrounding mantle [1,2]. A significant portion of diamonds contains black inclusions usually interpreted as graphite or sulphides. Twenty six dark inclusions from the 22 diamonds were exposed by polishing for chemical microanalysis. Inclusions were studied with SEM, TEM and EMP. Fe-C-O melt inclusions in association with with Kfsp, Ol and silicate melt inclusions were identified. Most of the inclusions are heterogeneous in composition and consist of iron carbides, iron in various oxidation states and carbon. Carbides contain impurities of Ni (0-0.6%), Sr (up to 3.4%), Cr (up to 0.8%) Si (up to 1%). Inclusions of wustite and Fe-Ti-O melt were identified in one diamond along with inclusions of Fe-C-O melt. In two cases diamond inclusions found within host diamond crystal. Diamond inclusions are surronded by a border consisting of wustite and siderite. Inclusions of Fe-C-O melt in allivial diamonds are best explained by carbonate melt-iron reaction [3].
Geochimica et Cosmochimica Acta, Vol. 266, pp. 197-212.
Russia, Urals
diamond inclusions
Abstract: The compositions of mineral inclusions from a representative collection (more than 140 samples) of diamonds from the placer deposits in the Ural Mountains were studied to examine their compositional diversity. The overwhelming majority of rounded octahedral and dodecahedral stones typical of placers contain eclogitic (E-type) mineral inclusions (up to 80%) represented by garnets with Mg# 40-75 and Ca# 10-56, including the unique high calcic “grospydite” composition, omphacitic pyroxenes containing up to 65% of jadeite, as well as kyanite, coesite, sulfides, and rutile. Peridotitic (P-type) inclusions are represented by olivine, subcalcic Cr-pyrope, chrome diopside, enstatite and magnesiochromite that are typical for diamonds worldwide. Comparing the chemical composition of olivine, pyrope and magnesiochromite in diamonds of the Urals, north-east of the Siberian platform placers and Arkhangelsk province kimberlites show striking similarity. There are significant differences only in the variations of carbon isotopic composition of the diamonds from the placers of the Urals and north-east of the Siberian platform. One typical rounded dodecahedral diamond was found to contain abundant primary oriented submicrometer-sized (<3.0?µm) octahedral fluid inclusions identified by transmission electron microscopy, which caused the milky color of the entire diamond crystal. The electron energy-loss spectrum of a singular inclusion has a peak at ?405?eV, indicating that nitrogen is present. The Raman spectra with peaks at 2346-2350?cm?1 confirmed that nitrogen exists in the solid state at room temperature. This means that fossilized pressure inside fluid inclusions may be over 6.0 GPa at room temperature, so the diamond may be considered sublithospheric in origin. However, identification of unique fluid inclusions in one typical placer diamond allows one to expand the pressure limit to at least more than 8.0 GPa. The volatile components of four diamonds from the Urals placers were analyzed by gas chromatography-mass spectrometry (GC-MS). They are represented (rel. %) by hydrocarbons and their derivatives (14.8-78.4), nitrogen and nitrogenated compounds (6.2-81.7), water (2.5-5.5), carbon dioxide (2.8-12.1), and sulfonated compounds (0.01-0.96). It is shown that high-molecular-weight hydrocarbons and their derivatives, including chlorinated, nitrogenated and sulfonated compounds, appear to be stable under upper mantle P-T conditions. A conclusion is drawn that Urals placer diamonds are of kimberlitic origin and are comparable in their high E-type/P-type inclusion ratios to those from the northeastern Siberian platform and in part to diamonds of the Arkhangelsk kimberlite province.
Abstract: The heat flux across the core-mantle boundary (QCMB) is the key parameter to understand the Earth/s thermal history and evolution. Mineralogical constraints of the QCMB require deciphering contributions of the lattice and radiative components to the thermal conductivity at high pressure and temperature in lower mantle phases with depth-dependent composition. Here we determine the radiative conductivity (krad) of a realistic lower mantle (pyrolite) in situ using an ultra-bright light probe and fast time-resolved spectroscopic techniques in laser-heated diamond anvil cells. We find that the mantle opacity increases critically upon heating to ~3000 K at 40-135 GPa, resulting in an unexpectedly low radiative conductivity decreasing with depth from ~0.8 W/m/K at 1000 km to ~0.35 W/m/K at the CMB, the latter being ~30 times smaller than the estimated lattice thermal conductivity at such conditions. Thus, radiative heat transport is blocked due to an increased optical absorption in the hot lower mantle resulting in a moderate CMB heat flow of ~8.5 TW, at odds with present estimates based on the mantle and core dynamics. This moderate rate of core cooling implies an inner core age of about 1 Gy and is compatible with both thermally- and compositionally-driven ancient geodynamo.
Abstract: Approximately 700 diamond crystals were identified in volcanic (mainly pyroclastic) rocks of the Tolbachik volcano, Kamchatka, Russia. They were studied with the use of SIMS, scanning and transmission electron microscopy, and utilization of electron energy loss spectroscopy and electron diffraction. Diamonds have cube-octahedral shape and extremely homogeneous internal structure. Two groups of impurity elements are distinguished by their distribution within the diamond. First group, N and H, the most common structural impurities in diamond, are distributed homogeneously. All other elements observed (Cl, F, O, S, Si, Al, Ca, and K) form local concentrations, implying the existence of inclusions, causing high concentrations of these elements. Most elements have concentrations 3-4 orders of magnitude less than chondritic values. Besides N and H, Si, F, Cl, and Na are relatively enriched because they are concentrated in micro- and nanoinclusions in diamond. Mineral inclusions in the studied diamonds are 70-450 nm in size, round- or oval-shaped. They are represented by two mineral groups: Mn-Ni alloys and silicides, with a wide range of concentrations for each group. Alloys vary in stoichiometry from MnNi to Mn2Ni, with a minor admixture of Si from 0 to 5.20-5.60 at%. Silicides, usually coexisting with alloys, vary in composition from (Mn,Ni)4Si to (Mn,Ni)5Si2 and Mn5Si2, and further to MnSi, forming pure Mn-silicides. Mineral inclusions have nanometer-sized bubbles that contain a fluid or a gas phase (F and O). Carbon isotopic compositions in diamonds vary from -21 to -29‰ ?13CVPDB (avg. = -25.4). Nitrogen isotopic compositions in diamond from Tolbachik volcano are from -2.32 to -2.58‰ ?15NAir. Geological, geochemical, and mineralogical data confirm the natural origin of studied Tolbachik diamonds from volcanic gases during the explosive stage of the eruption.
Abstract: We demonstrate for the first time the presence of iron carbides in placer diamonds from the northeastern region of the Siberian craton. It was found that the inclusions are polycrystalline aggregates, and iron carbides filling the fissures in the diamonds, thus providing clear evidence that the iron melts were captured first. Iron carbides were identified in diamonds containing mineral inclusions of eclogitic (Kfs, sulfide) and peridotitc (olivine) paragenesis. Iron carbides with minor amounts of admixed nickel were detected in a diamond sample containing an olivine inclusion (0.3 wt% Ni), indicating that the iron melt was not in equilibrium with the mantle peridotite.The low nickel contents of the iron carbides provide the best evidence that the subducted crust is a likely source of the iron melt. Diamonds containing carbide inclusions are characterised by a relatively low nitrogen aggregation state (5-35%), which is not consistent with the high temperature of the transition zone. Therefore, we have reason to assume that the studied diamonds are from the lower regions of the lithosphere. Considering all factors, the model for the interaction of the ascending asthenospheric mantle with the subducting slab seems to be more realistic.
Diamonds & Related Materials, in press available, 31p. Pdf
Global
carbon
Abstract: Natural diamonds that have been partially replaced by graphite have been observed to occur in natural rocks. While the graphite-to-diamond phase transition has been extensively studied the opposite of this (diamond to graphite) remains poorly understood. We performed high-pressure and temperature hydrous and anhydrous experiments up to 1.0?GPa and 1300?°C using Amplex premium virgin synthetic diamonds (20-40??m size) as the starting material mixed with Mg (OH)2 as a source of H2O for the hydrous experiments. The experiments revealed that the diamond-to-graphite transformation at P?=?1GPa and T?=?1300?°C was triggered by the presence of H2O and was accomplished through a three-stage process. Stage 1: diamond reacts with a supercritical H2O producing an intermediate 200-500?nm size “globular carbon” phase. This phase is a linear carbon chain; i.e. a polyyne or carbyne. Stage 2: the linear carbon chains are unstable and highly reactive, and they decompose by zigzagging and cross-linking to form sp2-bonded structures. Stage 3: normal, disordered, and onion-like graphite is produced by the decomposition of the sp-hybridized carbon chains which are re-organized into sp2 bonds. Our experiments show that there is no direct transformation from sp3 C-bonds into sp2 C-bonds. Our hydrous high-pressure and high-temperature experiments show that the diamond-to-graphite transformation requires an intermediate metastable phase of a linear hydrocarbon. This process provides a simple mechanism for the substitution of other elements into the graphite structure (e.g. H, S, O).
Mineralogy and Petrology, Vol. 115, 19p. Doi.org/101007 /s00710-020- 00723-x pdf
South America, Colombia
REE
Abstract: A multi-methodological study was conducted in order to provide further insight into the structural and compositional complexity of rare earth element (REE) fluorcarbonates, with particular attention to their correct assignment to a mineral species. Polycrystals from La Pita Mine, Municipality de Maripí, Boyacá Department, Colombia, show syntaxic intergrowth of parisite-(Ce) with röntgenite-(Ce) and a phase which is assigned to B3S4 (i.e., bastnäsite-3-synchisite-4; still unnamed) fluorcarbonate. Transmission electron microscope (TEM) images reveal well-ordered stacking patterns of two monoclinic polytypes of parisite-(Ce) as well as heavily disordered layer sequences with varying lattice fringe spacings. The crystal structure refinement from single crystal X-ray diffraction data - impeded by twinning, complex stacking patterns, sequential and compositional faults - indicates that the dominant parisite-(Ce) polytype M1 has space group Cc. Parisite-(Ce), the B3S4 phase and röntgenite-(Ce) show different BSE intensities from high to low. Raman spectroscopic analyses of parisite-(Ce), the B3S4 phase and röntgenite-(Ce) reveal different intensity ratios of the three symmetric CO3 stretching bands at around 1100 cm?1. We propose to non-destructively differentiate parisite-(Ce) and röntgenite-(Ce) by their 1092 cm?1 / 1081 cm?1 ?1(CO3) band height ratio.
Abstract: A multi-methodological study was conducted in order to provide further insight into the structural and compositional complexity of rare earth element (REE) fluorcarbonates, with particular attention to their correct assignment to a mineral species. Polycrystals from La Pita Mine, Municipality de Maripí, Boyacá Department, Colombia, show syntaxic intergrowth of parisite-(Ce) with röntgenite-(Ce) and a phase which is assigned to B3S4 (i.e., bastnäsite-3-synchisite-4; still unnamed) fluorcarbonate. Transmission electron microscope (TEM) images reveal well-ordered stacking patterns of two monoclinic polytypes of parisite-(Ce) as well as heavily disordered layer sequences with varying lattice fringe spacings. The crystal structure refinement from single crystal X-ray diffraction data - impeded by twinning, complex stacking patterns, sequential and compositional faults - indicates that the dominant parisite-(Ce) polytype M1 has space group Cc. Parisite-(Ce), the B3S4 phase and röntgenite-(Ce) show different BSE intensities from high to low. Raman spectroscopic analyses of parisite-(Ce), the B3S4 phase and röntgenite-(Ce) reveal different intensity ratios of the three symmetric CO3 stretching bands at around 1100 cm-1. We propose to non-destructively differentiate parisite-(Ce) and röntgenite-(Ce) by their 1092 cm-1 / 1081 cm-1 ?1(CO3) band height ratio.
Abstract: Ellinaite, a natural analog of the post-spinel phase ?-CaCr2O4, was discovered at the Hatrurim Basin, Hatrurim pyrometamorphic formation (the Mottled Zone), Israel, and in an inclusion within the super-deep diamond collected at the placer of the Sorriso River, Juína kimberlite field, Brazil. Ellinaite at the Hatrurim Basin is confined to a reduced rankinite-gehlenite paralava, where it occurs as subhedral grains up to 30?µm in association with gehlenite, rankinite and pyrrhotite or forms the rims overgrowing zoned chromite-magnesiochromite. The empirical formula of the Hatrurim sample is (Ca0.960FeNa0.012Mg0.003)0.992(Cr1.731VTiAl0.023TiO4. The mineral crystallizes in the orthorhombic system, space group Pnma, unit-cell parameters refined from X-ray single-crystal data: a 8.868(9), b 2.885(3), c 10.355(11)?Å, V 264.9(5)?Å3 and Z=4. The crystal structure of ellinaite from the Hatrurim Basin has been solved and refined to R1=0.0588 based on 388 independent observed reflections. Ellinaite in the Juína diamond occurs within the micron-sized polyphase inclusion in association with ferropericlase, magnesioferrite, orthorhombic MgCr2O4, unidentified iron carbide and graphite. Its empirical formula is Ca1.07(Cr1.71FeV0.06Ti0.03Al0.03Mg0.02Mn0.02)?1.93O4. The unit-cell parameters obtained from HRTEM data are as follows: space group Pnma, a 9.017, b 2.874?Å, c 10.170?Å, V 263.55?Å3, Z=4. Ellinaite belongs to a group of natural tunnel-structured oxides of the general formula AB2O4, the so-called post-spinel minerals: marokite CaMn2O4, xieite FeCr2O4, harmunite CaFe2O4, wernerkrauseite CaFeMn4+O6, chenmingite FeCr2O4, maohokite MgFe2O4 and tschaunerite Fe(FeTi)O4. The mineral from both occurrences seems to be crystallized under highly reduced conditions at high temperatures (>1000??C), but under different pressure: near-surface (Hatrurim Basin) and lower mantle (Juína diamond).
Geostandards and Geoanalytical Research, in press available
Technology
spectroscopy
Abstract: A broad suite of geological materials were studied a using a handheld laser-induced breakdown spectroscopy (LIBS) instrument. Because LIBS is simultaneously sensitive to all elements, the full broadband emission spectrum recorded from a single laser shot provides a ‘chemical fingerprint’ of any material - solid, liquid or gas. The distinguishing chemical characteristics of the samples analysed were identified through principal component analysis (PCA), which demonstrates how this technique for statistical analysis can be used to identify spectral differences between similar sample types based on minor and trace constituents. Partial least squares discriminant analysis (PLSDA) was used to distinguish and classify the materials, with excellent discrimination achieved for all sample types. This study illustrates through four selected examples involving carbonate minerals and rocks, the oxide mineral pair columbite-tantalite, the silicate mineral garnet and native gold how portable, handheld LIBS analysers can be used as a tool for real-time chemical analysis under simulated field conditions for element or mineral identification plus such applications as stratigraphic correlation, provenance determination and natural resources exploration.
Abstract: This manuscript presents results of the newest petrographic, mineralogical and bulk chemical, as well as H, C and O stable isotope study of carbonatites and associated silicate rocks from the Tajno Massif (NE Poland). The Tajno Intrusion is a Tournaisian-Visean ultramafic-alkaline-carbonatite body emplaced within the Paleoproterozoic rocks of the East European Craton (EEC). Carbonatites of the Tajno Massif can be subdivided into the calciocarbonatite (calcite), ferrocarbonatite (ankerite), and breccias with an ankerite-fluorite matrix. Due to location at the cratonic margin and abundance in the REE, Tajno classifies (Hou et al., 2015) as the carbonatite-associated REE deposit (CARD), and more precisely as the Dalucao-Style orebody (the breccia-hosted orebody). High Fe2O3 (13.8 wt%), MnO (2.1 wt%), total REE (6582 ppm), Sr (43895 ppm), Ba (6426 ppm), F (greater than10000 ppm) and CO2 contents points for the involvement of the slab - including pelagic metalliferous sediments - in the carbonatites formation. Spatial relations and Sr isotope composition ((87Sr/86Sr)i = 0.7043-0.7048; Wiszniewska et al., 2020) of alkali clinopyroxenite and syenite suggest that these are products of differentiation of the magma, generated by the initial melting of the SCLM due to influx of F-rich fluids from subducted marine sediments. Carbonatites Sr isotope composition ((87Sr/86Sr)i = 0.7037-0.7038), and Ba/Th (16-20620) and Nb/Y (0.01-6.25) ratios, link their origin with a more advanced melting of the SCLM, triggered by CO2-rich fluids from the subducted AOC and melts from sediments. The Tajno Massif - and coeval mafic-alkaline intrusions - age, high potassic composition, and location along the craton margin nearly parallel the Variscan deformation front, are suggesting Variscan subduction beneath the EEC. The oxygen isotope compositions of clinopyroxene (?18O value = 5.2‰) and alkali feldspar (?18O value = 5.7‰), from alkali clinopyroxenite and foid syenite, respectively, are consistent with mantle-derived magmas. Isotopic compositions of carbonatites and breccias (carbonate ?18O = 8.7‰ to 10.7‰; ?13C = -4.8‰ to ?0.4‰) span from values of primary carbonatites to carbonatites affected by a fractionation or sedimentary contamination. The highest values (?18O = 10.7‰; ?13C = -0.4‰) were reported for breccia cut by numerous veins confirming post-magmatic hydrothermal alteration. The lowest carbonate ?18O (9.3‰ to 10.7‰) and ?13C (?5.0‰ to ?3.8‰) values are reported for veins in alkali clinopyroxenites, whereas the highest ?18O (11.2‰) and ?13C (?1.2‰ to ?1.1‰) values are for veins in syenites and trachytes. Isotopic composition of veins suggests hydrothermal origin, and interaction with host mantle-derived rocks, as well as country rocks. In silicate rocks of the Tajno Massif, fluid influx leads to the development of Pb, Zn, Cu, Ag, Au sulfide mineralization-bearing stockwork vein system, with carbonate, silicate and fluorite infilling the veins. Bulk-rock contents of molybdenum (925 ppm), rhenium (905 ppb) and palladium (29 ppb) are notable. The Re-rich molybdenite association with galena, pyrite and Th-rich bastnäsite in carbonate veins is similar as in Mo deposits associated with carbonatites, implying the mantle source of Mo and Re.
Abstract: The Carboniferous sub-platform Tajno alkaline-carbonatite intrusion is located within a narrow alkaline magmatic belt, which trends E–W from SW Lithuania to NE Poland, along the southern rim of the Mesoproterozoic A–type Mazury Complex. The Tajno pluto–volcanic massif comprises clinopyroxenite cumulates and syenites that are crosscut by carbonatite veins of variable thickness. An emplacement age for the carbonatite has been obtained based on zircon U–Pb and pyrrhotite Re–Os from albitites crosscut by the intrusion. Both ages cluster at 354–345Ma, which corresponds to the Tournaisian Epoch of the Early Carboniferous Period. The carbonatite is 5 to 20Ma younger than the Kola Province, Russian Federation [1]. The current Tajno pluto-volcanic massif lies under ~600m of a Meso–Cenozoic cover. Carbonatite igneous systems are formed by processes of partial melting in metasomatised lithospheric mantle, and are associated with mantle plumes. This implies that a specific geochemical footprint may be spread throughout the host rocks and overlying sedimentary cover by post–emplacement processes. This is of key importance for carbonatite mineral exploration under cover. The Tajno carbonatitic veins do not contain typical accessory minerals (e.g. pyrochlore, perovskite, zirconolite, baddeleyite) that are classically found in other carbonatites. Instead, REE-bearing minerals such as burbankite, parisite, synchysite and bastnaesite are common. This explains its low Nb content. By contrast, fluorite is abundant as cement in the carbonatite breccia.This new study of alkaline-carbonatite rock assemblages is focused on: (1) characterise Tajno's isotopic, REE and HFSE footprint based on petrographic and geochemical observations of apatite and titanite; and (2) increase the understanding of Tajno–type carbonatitic intrusions in the region, and determine if such intrusions can be detected under the sedimentary cover by geochemical techniques. [1] Demaiffe et al.,(2013) The Journal of Geology 12, (1), 91–104
Central European carbonatites under cover: insights for mineral exploration from the Tajno alkaline intrusions, NE Poland.
Abstract: This Tajno alkaline massif (together with the nearby E?k and Pisz intrusions) occurs beneath a thick Mesozoic- Cenozoic sedimentary cover. It has first been recognized by geophysical (magnetic and gravity) investigations, then directly by deep drilling (12 boreholes down to 1800 m). The main rock types identified as clinopyroxenites, syenites, carbonatites, have been cut by later multiphase volcanic /subvolcanic dykes. This massif was characterized as a differentiated ultramafic, alkaline and carbonatite complex, quite comparable to the numerous massifs of the Late Devonian Kola Province of NW Russia [1,2]. Recent geochronological data (U-Pb on zircon from an albitite and Re-Os on pyrrhotite from a carbonatite) indicate that the massif was emplaced at ca. 348 Ma (Early Carboniferous). All the rocks, but more specifically the carbonatites, are enriched in Sr, Ba and LREE, like many carbonatites worldwide but depleted in high field strength elements (Ti, Nb, Ta, Zr). The initial 87Sr/86Sr (0.70370 to 0.70380) and ?Nd(t) (+3.3 to +0.7) isotopic compositions of carbonatites plot in the depleted quadrant of the Nd-Sr diagram, close to “FOcal ZOne” (FOZO) deep mantle domain [1]. The Pb isotopic data (206Pb/204Pb <18.50) do not point to an HIMU (high U/Pb) source. The ranges of C and O stable isotopic compositions of the carbonatites are quite large; some data plot in (or close to) the “Primary Igneous Carbonatite” box while others extend to much higher, typically crustal ?18O and ?13C values.
Dasgupta, R., Hirschmann, M.M., McDonough, W.F., Spiegelman, M., Withers, A.C.
Trace element partitioning between garnet lherzolite and carbonatite at 6.6 and 8.6 GPa with application to the geochemistry of the mantle and mantle derived melts
Chemical Geology, Vol. 262, 1-2, May 15, pp. 57-77.
Hydrogen partitioning between nominally anhydrous upper mantle minerals and melt between 3 and 5 GPa and applications to hydrous peridotite partial melting.
Chemical Geology, Vol. 262, 1-2, May 15, pp. 42-56.
Geological Society of London Special Publication Supercontinent Cycles through Earth History., Vol. 424, pp. 47-81.
Australia
Supercontinents
Abstract: The Australian continent records c. 1860-1800 Ma orogenesis associated with rapid accretion of several ribbon micro-continents along the southern and eastern margins of the proto-North Australian Craton during Nuna assembly. The boundaries of these accreted micro-continents are imaged in crustal-scale seismic reflection data, and regional gravity and aeromagnetic datasets. Continental growth (c. 1860-1850 Ma) along the southern margin of the proto-North Australian Craton is recorded by the accretion of a micro-continent that included the Aileron Terrane (northern Arunta Inlier) and the Gawler Craton. Eastward growth of the North Australian Craton occurred during the accretion of the Numil Terrane and the Abingdon Seismic Province, which forms part of a broader zone of collision between the northwestern margins of Laurentia and the proto-North Australian Craton. The Tickalara Arc initially accreted with the Kimberley Craton at c. 1850 Ma and together these collided with the proto-North Australian Craton at c. 1820 Ma. Collision between the West Australian Craton and the proto-North Australian Craton at c. 1790-1760 Ma terminated the rapid growth of the Australian continent.
Abstract: The late Mesoproterozoic Ngualla carbonatite complex in southwest Tanzania comprises a central magnesiocarbonatite plug surrounded sequentially by an annular calcite carbonatite intrusion and fenitised felsic igneous country rocks. The calcite carbonatite contains phlogopite-rich (glimmerite) enclaves interpreted as fenitised wallrock xenoliths that have contributed silicate minerals, apatite and magnetite through dispersal and interaction, mainly within the calcite carbonatite magma. Ultramafic magmas were emplaced into the magnesiocarbonatite magma chamber before complete solidification of the magnesiocarbonatite. Contemporaneity allowed the two magmas to mingle. Rounded enclaves of hematite-barite in the magnesiocarbonatite are tentatively attributed to magma immiscibility. Following complete solidification of the calcite carbonatite, and overlapping late crystallization of the magnesiocarbonatite plug, late magnesiocarbonatite dikes and ultramafic dikes were emplaced, some of the latter as diatremes. Crystallization of ferroan dolomite in the magnesiocarbonatite plug resulted in residual magmatic concentration of Si, Ba, F and rare earth elements (REE), and crystallization of barite, quartz, calcite, fluorite and REE fluorocarbonates in miarolitic cavities. Concentrations of (total) rare earth oxides (TREO) in the unweathered magnesiocarbonatite are 1 to 2%. REE ore with 3 to 6% TREO resulted from weathering, during which CaCO3 and MgCO3 were leached from ferroan dolomite leaving a porous goethite-rich residue containing barite and bastnaesite, the latter having replaced primary synchesite. Other commodities with potential economic significance include phosphate and niobium, both of which were enriched by residual accumulation over the calcite carbonatite as a result of karstic weathering. Although weathering was a critical factor in the formation of REE ore at Ngualla, the primary proto-ore resulted mainly from in situ igneous processes. This genetic model is different from that used to account for many carbonatite-hosted ore bodies, which result from late-stage hydrothermal processes. Examples of hydrothermal rare earth deposits include those of the late Jurassic to early Cretaceous Chilwa Province, located 800?km south of Ngualla. The differences in ore-forming processes may reflect the relative ages of the carbonatites and a deeper level of erosion at Ngualla.
The effect of temperature on the equilibrium distribution of trace elements between clinopyroxene, orthopyroxene, olivine and spinel in upper mantle peridotite.
The effect of temperature on the equilibrium distribution of trace elements between clinopyroxene, orthopyroxene, olivine and spinel in upper mantle peridotite.
Chemical geology, Vol. 221, 1-2, Sept. 5, pp. 65-101.
Wittig, N., Pearson, D.G., Downes, H., Baker, J.A.
The U, Th and Pb elemental and isotope compositions of mantle clinopyroxenes and their grain boundary contamination derived from leaching and digestion experiments.
Geochimica et Cosmochimica Acta, Vol. 73, 2, pp. 469-488.
Wittig, N., Webb, M., Pearson, D.G., Dale, C.W., Ottley, C.J., Hutchison, M., Jensen, S.M., Luget, A.
Formation of the North Atlantic craton: timing and mechanisms constrained from Re-Os isotope and PGE dat a of peridotite xenoliths from S.W. Greenland.
Wittig, N., Webb, M., Pearson, D.G., Dale, C.W., Ottley, C.J., Hutchison, M., Jensen, S.M., Luget, A.
Formation of the North Atlantic craton: timing and mechanisms constrained from Re-Os isotope and PGE dat a of peridotite xenoliths from S.W. Greenland.
Characterising modal metasomatic processes in young continental lithospheric mantle: a microsampling isotopic and trace element study on xenoliths from the Middle Atlas Mountains, Morocco.
Contributions to Mineralogy and Petrology, Vol. 162, 2, pp. 289-302.
Abstract: Calcium isotope compositions are presented for two suites of carbonatites and associated alkaline silicate rocks from Neoproterozoic Sevattur and Samalpatti complexes in Tamil Nadu, South India. Despite their geographic proximity, the mean G44/40Ca values are different for Sevattur (G44/40Ca = 0.69 r 0.10‰, n = 7) and Samalpatti (0.81 r 0.16‰, n = 5). The former suite is derived from an enriched mantle source without significant post-emplacement modifications [1] and its Ca isotope composition falls to the lower end of Ca isotope range reported for mantle-derived rocks [2]. Some carbonatites from Samalpatti show a 44Ca-enriched signature which could reflect large-scale low-temperature modification, recognized also by their 13C–18O-enriched isotope systematics and sizeable loss of REE, when compared to pristine carbonatites from the area [1]. This is also consistent with albite–epidote metasomatic sample and shistose pyroxenite from Samalpatti, both showing a 44Ca-depleted signature. Leaching experiments confirm a systematic G44/40Ca offset with isotopically light carbonate relative to bulk sample [also 3]. Pyroxenites from Samalpatti are isotopically heavier than accompanying unmodified carbonatites and their G44/40Ca values fall into the mantle range. In contrast, pyroxenite and phosphate from Sevattur have a G44/40Ca value identical with associated carbonatites, indicating a homogeneous mantle source for the latter complex. For K-rich syenites and monzonites, 40K-decay corrections need to be considered for the intrinsic mass-dependent isotope fractionations considering the Neoproterozoic age and high K/Ca character of some samples.
Magna, T., Rapprich, V., Wittke, A., Gussone, N., Upadhyay, D., Mikova, J., Pecskay, Z.
Calcium isotope systematics and K-Ar and U-Pb temporal constraints on the genesis of Sevattur Samalpatti carbonatite silicate alkaline complexes.
Carbonatite-alkaline rocks and associated mineral deposits , Dec. 8-11, abstract p. 34-35.
India
deposit - Samalpatti, Sevattur
Abstract: We present the first systematic survey of Ca isotope compositions in carbonatites and associated silicate rocks from Samalpatti and Sevattur, two Neoproterozoic complexes in Tamil Nadu, south India. Despite their close geographic proximity, their genesis and post-emplacement histories differ (Ackerman et al. 2017). The Sevattur complex appears to have been derived from an enriched mantle source with a limited post-magmatic disturbance. In contrast, carbonatites from Samalpatti show a record of extensive late-stage post-magmatic overprint, also apparent from unusually heavy C-O isotope compositions in a sub-suite of carbonatites (Ackerman et al. 2017). The mean ?44/40Ca = 0.69 ± 0.10‰ is slightly lighter than the average of fertile, unmetasomatized peridotites at ?44/40Ca = 0.95 ± 0.05‰ (Kang et al. 2017). This difference may attest to the general difference between carbonates and silicates (see Kang et al. 2017). It could also reflect Ca isotope fractionation between isotopically heavy silicate and isotopically light carbonate (e.g., John et al. 2012), though to a somewhat minor extent. This is supported by leaching experiments in this study where the extent of silicate-carbonate fractionation (44/40Casilicate-carbonate) has been investigated. The values at ~0.1-0.2‰ are expectedly lower than those reported earlier (~0.6‰; John et al. 2012) and may reflect high-temperature Ca isotope fractionation. The variability in ?44/40Ca values of carbonatites and silico-carbonatites from the Samalpatti complex is larger (0.70- 1.14‰) and appears to be in accord with extensive post-emplacement disturbance. Significant loss of REE and 13C-18O-enriched signature are combined with high ?44/40Ca values, which could reflect massive exchange with metasomatic aqueous fluids. The 40Kdecay correction was applied to K-rich rocks (syenites, monzonites). Given the antiquity of the complex dated at ca. ~800 Ma (Schleicher et al. 1997) and considering high-K/Ca character of some rocks, the resulting ?44/40Ca800 Myr correction was up to ~+1.2‰. In this regard, it is crucial to constrain the age history of the entire region. The nearby Hogenakal carbonatite body was dated at ~2.4 Ga which is much older than Rb-Sr and Sm-Nd age of Sevattur (Kumar et al. 1998) from the same fault system. We have acquired K-Ar mineral (K-feldspar, biotite, amphibole) and U-Pb zircon data from Sevattur and Samalpatti. The K-Ar ages span a range between ~800 and ~510 Ma (~800 Ma for amphiboles and biotites from silico-carbonatites and mafic silicate rocks and ~570-510 Ma for K-feldspars and biotites from syenites), dating two high-grade regional tectono-thermal overprint events, documented earlier. The complex nature of this process is indicated by concordant U-Pb zircon age at ~2.5 Ga yielded for a melatonalite, for which K-Ar biotite age of ~802 Ma was measured. This fits into the age bracket of basement of the Eastern Dharwar Craton. The age distribution bimodality at ~2.5 Ga and ~800 Ma has been found for several other samples, suggesting a pulsed thermal history of the area, associated with a significant overprint by fluids likely derived from the local crust. Particularly high U concentrations in zircons (thousands ppm), combined with a range of K-Ar ages, attest to such multi-episodic history.
Earth and Planetary Science Letters, Vol. 478, pp. 52-58.
Canada, Quebec
Mistastin crater
Abstract: Bolide impacts influence primordial evolution of planetary bodies because they can cause instantaneous melting and vaporization of both crust and impactors. Temperatures reached by impact-generated silicate melts are unknown because meteorite impacts are ephemeral, and established mineral and rock thermometers have limited temperature ranges. Consequently, impact melt temperatures in global bombardment models of the early Earth and Moon are poorly constrained, and may not accurately predict the survival, stabilization, geochemical evolution and cooling of early crustal materials. Here we show geological evidence for the transformation of zircon to cubic zirconia plus silica in impact melt from the 28 km diameter Mistastin Lake crater, Canada, which requires super-heating in excess of 2370?°C. This new temperature determination is the highest recorded from any crustal rock. Our phase heritage approach extends the thermometry range for impact melts by several hundred degrees, more closely bridging the gap between nature and theory. Profusion of >2370?°C superheated impact melt during high intensity bombardment of Hadean Earth likely facilitated consumption of early-formed crustal rocks and minerals, widespread volatilization of various species, including hydrates, and formation of dry, rigid, refractory crust.
Abstract: Something strange is going on at the top of the world. Earth’s north magnetic pole has been skittering away from Canada and towards Siberia, driven by liquid iron sloshing within the planet’s core. The magnetic pole is moving so quickly that it has forced the world’s geomagnetism experts into a rare move. On 15 January, they are set to update the World Magnetic Model, which describes the planet’s magnetic field and underlies all modern navigation, from the systems that steer ships at sea to Google Maps on smartphones. The most recent version of the model came out in 2015 and was supposed to last until 2020 — but the magnetic field is changing so rapidly that researchers have to fix the model now. “The error is increasing all the time,” says Arnaud Chulliat, a geomagnetist at the University of Colorado Boulder and the National Oceanic and Atmospheric Administration’s (NOAA’s) National Centers for Environmental Information. The problem lies partly with the moving pole and partly with other shifts deep within the planet. Liquid churning in Earth’s core generates most of the magnetic field, which varies over time as the deep flows change. In 2016, for instance, part of the magnetic field temporarily accelerated deep under northern South America and the eastern Pacific Ocean. Satellites such as the European Space Agency’s Swarm mission tracked the shift. By early 2018, the World Magnetic Model was in trouble. Researchers from NOAA and the British Geological Survey in Edinburgh had been doing their annual check of how well the model was capturing all the variations in Earth’s magnetic field. They realized that it was so inaccurate that it was about to exceed the acceptable limit for navigational errors.
Abstract: Many carbonatites are associated both spatially and temporally with large igneous provinces (LIPs), and considered to originate from a mantle plume source lacking any contribution from recycled crustal materials. Here, we report an occurrence of carbonatite enriched in rare-earth elements (REE) and associated with the Tarim LIP in northwestern China. The Tarim LIP comprises intrusive and volcanic products of mantle plume activity spanning from ~ 300 to 280 Ma. The carbonatites at Wajilitage in the northwestern part of Tarim are dominated by calcite and dolomite varieties, and contain abundant REE minerals (principally, monazite and REE-fluorcarbonates). Th-Pb age determination of monazite yielded an emplacement age of 266 ± 5.3 Ma, i.e. appreciably younger than the eruption age of flood basalts at ~ 290 Ma. The carbonatites show low initial 87Sr/86Sr (0.7037-0.7041) and high ?Nd(t) (1.2-4) values, which depart from the isotopic characteristics of plume-derived basalts and high-Mg picrites from the same area. This indicates that the Wajilitage carbonatites derived from a mantle source isotopically distinct from the one responsible for the voluminous (ultra)mafic volcanism at Tarim. The carbonatites show ?26MgDSM3 values (? 0.99 to ? 0.65‰) that are significantly lower than those in typical mantle-derived rocks and rift carbonatites, but close to marine sediments and orogenic carbonatites. We propose that the carbonatites in the Tarim LIP formed by decompressional melting of recycled sediments mixed with the ambient mantle peridotite. The enriched components in the Tarim plume could be accounted for by the presence of recycled sedimentary components in the subcontinental mantle.
Harper, C.T., Van Breeman, O., Wodick,N., Pehrsson, S., Heaman, L., Hartlaub, R.
The Paleoproterozoic lithostructural history and thermotectonic reactivation of the Archean basement in southern Hearne domain of northeastern Saskatchewan.
GAC Annual Meeting Halifax May 15-19, Abstract 1p.
The Trans Hudson Orogen of North America and the Himalayan Karakoram Tibetan Orogen of Asia: structural and thermal evolution of the lower and upper plates.
GAC Annual Meeting Halifax May 15-19, Abstract 1p.
Trans Hudson Orogen of North America and Himalaya Karakoram Tibetan Orogen of Asia: structural and thermal characteristics of the lower and upper plates.
Abstract: There are lingering questions about how far back in geologic time plate tectonic processes began. In the Paleoproterozoic of eastern Laurentia, accretion of intra-oceanic juvenile terranes along the leading edge of the Superior craton apex (Ungava indenter) during the interval 1.87-1.83 Ga was followed by collision with the Churchill plate at ca. 1.83-1.79 Ga. Orthogonal shortening along the indenter led to early obduction of the juvenile terranes including the ca. 2.0 Ga Watts Group ophiolite, followed by out-of-sequence thrusting at ca. 1.83 Ga of granulite-facies crystalline basement of the Sugluk block (Churchill plate) along the Sugluk suture. Exhumation and erosion of the Sugluk block led to deposition of a foreland/delta fan sequence in the Hudson Bay re-entrant (Omarolluk and Loaf formations of the Belcher Group), with detritus sourced exclusively from the Sugluk block. Continued collision led to critical wedge development and orocline formation in the Hudson Bay re-entrant, forming a strongly arcuate fold-thrust belt. On the other (eastern) side of the indenter, material flow during crustal shortening was accommodated by lateral extrusion of microplates towards a then open ocean basin, in a manner similar to present-day extrusion of Indochina as a response to India - South China craton convergence. In the Churchill plate hinterland W-NW of the indenter, propagating strike-slip faults resulted in the far-field extrusion and oblique exhumation of Archean crustal slices of the Rae crustal block. The 1.83-1.79 Ga Superior-Churchill collision accommodated a minimum of 500 km of continent-continent convergence, with resulting style and mechanisms of orogenic growth and material flow similar to those observed in the Alpine-Himalayan orogenic system.
Contributions to Mineralogy and Petrology, Vol. 174, 4, doi.org/10. 1007/s00410-018-1530-x 13p.
Mantle
carbonatite
Abstract: Here we present an experimental study of the distribution of a broad range of trace elements between carbonatite melt, calcite and fluorite. The experiments were performed in the CaCO3 + CaF2 + Na2CO3 ± Ca3(PO4)2 synthetic system at 650-900 °C and 100 MPa using rapid-quench cold-seal pressure vessels. Starting mixtures were composed of reagent-grade oxides, carbonates, Ca3(PO4)2 and CaF2 doped with 1 wt% REE-HFSE mixture. The results show that the distribution coefficients of all the analyzed trace elements for calcite and fluorite are below 1, with the highest values observed for Sr (0.48-0.8 for calcite and 0.14-0.3 for fluorite) and Y (0.18-0.3). The partition coefficients of REE gradually increase with increasing atomic number from La to Lu. The solubility of Zr, Hf, Nb and Ta in the synthetic F-rich carbonatitic melts, which were used in our experiments, is low and limited by crystallization of baddeleyite and Nb-bearing perovskite.
Physics and Chemistry of Minerals, doi.org/10.1007/s00269-018-0995-5 16p.
Mantle
carbonatite
Abstract: Thermodynamic modeling offers a powerful framework for studying melting reactions of carbonated mantle systems across a wide range of compositions, pressures, and temperatures. Such modeling requires knowledge of the standard state thermodynamic properties of the pure alkaline earth carbonate liquid components, which are difficult to determine experimentally due to their instability at 1 bar. Atomistic simulations offer a solution to these experimental difficulties by providing access to metastable states and supplying constraints on thermodynamic properties. We developed an empirically-derived potential model for the simulation of alkaline earth carbonates (MgCO3, CaCO3, SrCO3 and BaCO3), emphasizing the accurate simulation of the standard state thermodynamic properties of carbonate liquids. Molecular dynamics (MD) simulations of liquids in the CaCO3-SrCO3-BaCO3 system are performed over a geologically relevant temperature-pressure range (1100-3400 K and 0-43 GPa). Simulation data for each of these three components (up to a maximum of 2300 K and 30 GPa) are fitted to a temperature-dependent third-order Birch-Murnaghan equation-of-state to estimate their standard state thermodynamic properties. With a few exceptions, calculated properties agree well with available estimates from experiments and/or first-principles MD simulations. Exploration of binary mixtures supports ideal mixing of volumes, heat capacities, and compressibilities, reflecting the common liquid structure and pressure-temperature evolution for these three components. The success of this new model for CaCO3-SrCO3-BaCO3 liquids suggests that it can accurately predict the properties of MgCO3-bearing liquids, where experimental data are unavailable.
Earth and Planetary Science Letters, Vol. 531, 10p. Pdf
Mantle
carbonatite
Abstract: MgCO3 is one of the most important components of mantle-derived carbonatite melts, and yet also one of the most difficult to study experimentally. Attempts to constrain its thermodynamic properties are hampered by decarbonation, which occurs at only ?500 °C, far below its metastable 1 bar melting temperature. Molecular dynamic simulations, however, can predict the thermodynamic properties of the MgCO3 liquid component in spite of experimental challenges. Using the recently developed empirical potential model for high-pressure alkaline-earth carbonate liquids (Hurt and Wolf, 2018), we simulate melts in the MgCO3-CaCO3-SrCO3-BaCO3 system from 773 to 2373 K up to 20 GPa. At 1 bar, MgCO3 liquid assumes a novel topology characterized by a 4-fold coordination of the metal cation (Mg) with both the carbonate molecule and oxygen ion; this is distinct from the other alkaline-earth carbonate liquids in which the metal cation is in ?6- and ?8-fold coordination with carbonate and oxygen. With increasing pressure, MgCO3 liquid structure becomes progressively more like that of (Ca, Sr, Ba)CO3 liquids with approaching 6-fold coordination with carbonate groups. The novel network topology of MgCO3 liquid results in a melt that is significantly more buoyant and compressible than other alkaline-earth carbonate liquids. Simulations of mixed MgCO3-bearing melts show that metal cation coordination with O and C is independent of bulk composition. Mixed simulation also reveal that molar volume, compressibility, enthalpy and heat capacity do not mix ideally with (Ca, Sr, Ba)CO3 liquids at 1 bar, a consequence of preferential metal-cation ordering in MgCO3-bearing mixtures. As pressure increases, however, mixing progressively approaches ideality with respect to molar volume, becoming nearly ideal by 12 GPa. The model is further applied to mantle-derived primary carbonatite melts with compositions, temperatures and pressures determined by published phase equilibrium experiments. The voluminous structure of liquid MgCO3 results in a buoyant melt that inhibits a density crossover with the surrounding mantle. Assuming FeCO3 liquid also adopts the same anomalous high-volume structure as MgCO3, we predict that even the most Fe-rich ferrocarbonatites would remain buoyant and be barred from sinking or stagnating in the mantle.
Abstract: Although plate tectonics has pushed the frontiers of geosciences in the past 50 years, it has legitimate limitations and among them we focus on both the absence of dynamics in the theory, and the difficulty of reconstructing tectonics when data is sparse. In this manuscript, we propose an anticipation experiment, proposing a singular outlook on plate tectonics in the digital era. We hypothesize that mantle convection models producing self?consistently plate?like behavior will capture the essence of the self?organisation of plate boundaries. Such models exist today in a preliminary fashion and we use them here to build a database of mid?ocean ridge and trench configurations. To extract knowledge from it we develop a machine learning framework based on Generative Adversarial Networks (GANs) that learns the regularities of the self?organisation in order to fill gaps of observations when working on reconstructing a plate configuration. The user provides the distribution of known ridges and trenches, the location of the region where observations lack, and our digital architecture proposes a horizontal divergence map from which missing plate boundaries are extracted. Our framework is able to prolongate and interpolate plate boundaries within an unresolved region, but fails to retrieve a plate boundary that would be completely contained inside of it. The attempt we make is certainly too early because geodynamic models need improvement and a larger amount of geodynamic model outputs, as independent as possible, is required. However, this work suggests applying such an approach to expand the capabilities of plate tectonics is within reach.
Earth and Planetary Science Letters, in press available 8p. Pdf
Mantle
subduction
Abstract: Long-term patterns of mantle convection are illustrated by the locations of large low-shear-velocity provinces (LLSVPs) in the lowermost mantle, as well as an enclosing girdle of subduction zones. These structures, stable since Pangea's breakup, have been proposed to provide an absolute reference frame to anchor plate motions in deep time. Simple conceptual models of the supercontinent cycle (introversion, extroversion, orthoversion) predict differing loci of global subduction zones and inferred LLSVPs. We develop a tool to statistically compare idealized supercontinent cycle models with paleolatitude distributions of global subduction zones from paleogeographic reconstructions. We find that subduction zone locations younger than 250 Ma are moderately well described by an idealized girdle around the LLSVPs, but more robust conceptual models must take into account a Tethyan locus or “arm” within the girdle. Between 540 and 250 Ma, such an orthogonal arm is not needed to generate robust correlations with paleogeography; but the global subduction girdle is found to rotate progressively by approximately 90°. Our results suggest that planetary degree-two mantle structures are long-lived but not eternal: they reorganize their absolute locations from one supercontinent cycle to the next.
Earth and planetary Science Letters, Vol. 578, 117293, 8p.
Pangea
subduction
Abstract: Long-term patterns of mantle convection are illustrated by the locations of large low-shear-velocity provinces (LLSVPs) in the lowermost mantle, as well as an enclosing girdle of subduction zones. These structures, stable since Pangea's breakup, have been proposed to provide an absolute reference frame to anchor plate motions in deep time. Simple conceptual models of the supercontinent cycle (introversion, extroversion, orthoversion) predict differing loci of global subduction zones and inferred LLSVPs. We develop a tool to statistically compare idealized supercontinent cycle models with paleolatitude distributions of global subduction zones from paleogeographic reconstructions. We find that subduction zone locations younger than 250 Ma are moderately well described by an idealized girdle around the LLSVPs, but more robust conceptual models must take into account a Tethyan locus or “arm” within the girdle. Between 540 and 250 Ma, such an orthogonal arm is not needed to generate robust correlations with paleogeography; but the global subduction girdle is found to rotate progressively by approximately 90°. Our results suggest that planetary degree-two mantle structures are long-lived but not eternal: they reorganize their absolute locations from one supercontinent cycle to the next.
Abstract: Eocene paleoclimate reconstructions are rarely accompanied by parallel estimates of CO2 from the same locality, complicating assessment of the equilibrium climate response to elevated CO2. We reconstruct temperature, precipitation, and CO2 from latest middle Eocene (ca. 38 Ma) terrestrial sediments in the posteruptive sediment fill of the Giraffe kimberlite in subarctic Canada. Mutual climatic range and oxygen isotope analyses of botanical fossils reveal a humid-temperate forest ecosystem with mean annual temperatures (MATs) more than 17 °C warmer than present and mean annual precipitation ?4× present. Metasequoia stomatal indices and gas-exchange modeling produce median CO2 concentrations of ?630 and ?430 ppm, respectively, with a combined median estimate of ?490 ppm. Reconstructed MATs are more than 6 °C warmer than those produced by Eocene climate models forced at 560 ppm CO2. Estimates of regional climate sensitivity, expressed as ?MAT per CO2 doubling above preindustrial levels, converge on a value of ?13 °C, underscoring the capacity for exceptional polar amplification of warming and hydrological intensification under modest CO2 concentrations once both fast and slow feedbacks become expressed.
45th. Annual Yellowknife Geoscience Forum, p. 65 abstract
Canada, Northwest Territories
deposit - Giraffe
Abstract: Several Lac de Gras kimberlite pipes host thick accumulations of stratified post-eruptive lacustrine sediment and peat. Given the range of Lac de Gras kimberlite emplacement ages, these fills - though rare - provide a unique sedimentary archive of paleoenvironments during the sustained Early Cenozoic “greenhouse” interval, in a high-latitude region otherwise devoid of Phanerozoic sediment cover. Extensive exploration drilling has provided a valuable window into this unique sedimentary record, which would have otherwise remained covered by Quaternary glacial deposits. Our focus to date has been multidisciplinary study of the Giraffe pipe sediment fill: an ~80 m-thick sequence of post-eruptive lacustrine silt overlain by peat, which paints a remarkable picture of a humid-temperate Middle Eocene forest ecosystem on the Canadian Shield. Post-eruptive chronology is provided by interbedded distal tephra horizons, likely sourced from Alaska, that have been dated by glass fission-track and zircon U-Pb techniques. Paleoclimate proxies derived from pollen, wood cellulose oxygen isotopes, and biomarkers converge on reconstructed mean annual temperatures >17 °C warmer than present, with mean winter temperatures above freezing, and mean annual precipitation ~4x present. Two independent reconstructions of CO2 from well preserved conifer foliage suggest that this warming occurred under relatively modest atmospheric CO2 concentrations of 430-630 ppm. These findings provide direct field-based evidence for dramatic past arctic warming at CO2 concentrations that were well within the range of projections under “business-as-usual” emissions scenarios, underscoring the capacity for exceptional polar amplification of climate change under modest CO2 concentrations once both fast and slow feedbacks processes become expressed. Our studies at Giraffe pipe also highlight the scientific value of archived exploration drill core in the Lac de Gras kimberlite field, particularly with respect to pipes that are unremarkable for the purpose of diamond exploration.
Abstract: This article empirically investigates the relationship between price dispersion and price level. Searches seem more valuable for products of high quality, but buyers may have little incentive to search since such products are less frequently purchased. The extent of price dispersion is examined using a sample of around 160 000 diamonds offered for sale online. Estimates from a two-stage econometric strategy show that price dispersion increases significantly with quality. An explanation is that buyers of high-quality gemstones pay little attention to the price of these diamonds and even more so if they perceive high prices as signals of quality and rarity of the diamonds they intend to purchase.
Annals of Operations Research, Vol. 244, 2, pp. 0254-5330.
Global
Economics
Abstract: This paper investigates the relative efficiency of buyers and sellers on the online diamond market using a non-parametric double-frontier setting. Our data consists in a sample of more than 100,000 round cut diamonds offered for sale online. For a given quality defined by a combination of color and clarity grades, we turn to the free disposal hull model to estimate the sets of efficient diamonds respectively for buyers and sellers in the price-weight space. We find that the average bargaining power of buyers is lower than that of sellers. Regression estimates show that the relative efficiency of buyers is reduced for heavier diamonds and when there are many diamonds of the same quality offered for sale.
New developments in diamond recovery and security procedures - preserving the dollars. Excellent pictoral- x-ray and optical sorting, material handling
Diamonds in Kimberley Symposium & Trade Show, Bristow and De Wit held August 23-24, Kimberley, South Africa, GSSA Diamond Workshop CD slides 1-94.
Abstract: Earth’s volatile element abundances (for example, sulfur, zinc, indium and lead) provide constraints on fundamental processes, such as planetary accretion, differentiation and the delivery of volatile species, like water, which contributed to Earth becoming a habitable planet. The composition of the silicate Earth suggests a chemical affinity but isotopic disparity to carbonaceous chondrites—meteorites that record the early element fractionations in the protoplanetary disk. However, the volatile element depletion pattern of the silicate Earth is obscured by core formation. Another key problem is the overabundance of indium, which could not be reconciled with any known chondrite group. Here we complement recently published volatile element abundances for carbonaceous chondrites with high-precision sulfur, selenium and tellurium data. We show that both Earth and carbonaceous chondrites exhibit a unique hockey stick volatile element depletion pattern in which volatile elements with low condensation temperatures (750-500?K) are unfractionated from each other. This abundance plateau accounts for the apparent overabundance of indium in the silicate Earth without the need of exotic building materials or vaporization from precursors or during the Moon-forming impact and suggests the accretion of 10-15?wt% CI-like material before core formation ceased. Finally, more accurate estimates of volatile element abundances in the core and bulk Earth can now be provided.
Geochimica et Cosmochinica Acta, Vol. 213, pp. 574-592.
Africa, Botswana
deposit - Orapa
Abstract: Major- and trace-element compositions of garnet and clinopyroxene, as well as 87Sr/86Sr in clinopyroxene and ?18O in garnet in eclogite and pyroxenite xenoliths from Orapa, at the western margin of the Zimbabwe craton (central Botswana), were investigated in order to trace their origin and evolution in the mantle lithosphere. Two groups of eclogites are distinguished with respect to 87Sr/86Sr: One with moderate ratios (0.7026-0.7046) and another with 87Sr/86Sr >0.7048 to 0.7091. In the former group, heavy ?18O attests to low-temperature alteration on the ocean floor, while 87Sr/86Sr correlates with indices of low-pressure igneous processes (Eu/Eu?, Mg#, Sr/Y). This suggests relatively undisturbed long-term ingrowth of 87Sr at near-igneous Rb/Sr after metamorphism, despite the exposed craton margin setting. The high-87Sr/86Sr group has mainly mantle-like ?18O and is suggested to have interacted with a small-volume melt derived from an aged phlogopite-rich metasome. The overlap of diamondiferous and graphite-bearing eclogites and pyroxenites over a pressure interval of ?3.2 to 4.9 GPa is interpreted as reflecting a mantle parcel beneath Orapa that has moved out of the diamond stability field, due to a change in geotherm and/or decompression. Diamondiferous eclogites record lower median 87Sr/86Sr (0.7039) than graphite-bearing samples (0.7064) and carbon-free samples (0.7051), suggesting that interaction with the - possibly oxidising - metasome-derived melt caused carbon removal in some eclogites, while catalysing the conversion of diamond to graphite in others. This highlights the role of small-volume melts in modulating the lithospheric carbon cycle. Compared to diamondiferous eclogites, eclogitic inclusions in diamonds are restricted to high FeO and low SiO2, CaO and Na2O contents, they record higher equilibrium temperatures and garnets have mostly mantle-like O isotopic composition. We suggest that this signature was imparted by a sublithospheric melt with contributions from a clinopyroxene-rich source, possibly related to the ca. 2.0 Ga Bushveld event.
Mineralogical Magazine, Vol. 81, 6, pp. 1551-1576.
Australia
mineralogy
Abstract: View at publisher (open access)
Abstract
Significant uncertainty surrounds the processes involved in the formation of basalt-hosted corundum, particularly the role that the mantle plays in corundum generation. Some previous studies have suggested that trace-element ratios (namely, Cr/Ga and Ga/Mg) are useful for distinguishing two types of corundum: “magmatic” and “metamorphic,” designations that include mantle and crustal processes. However, recent studies, including this one, have discovered transitional groups between these end-members that are difficult to classify. We used LA-ICP-MS to measure trace-element concentrations in sapphire and ruby crystals from eight alluvial deposits that span a significant length of the eastern Australian gemstone belt. Additionally, we collected LA-ICP-MS U-Pb and trace-element data from zircon megacrysts at Weldborough, Tasmania, which is also within the gemstone belt. Our sapphire and ruby results reveal a continuum in trace-element compositions, a finding that raises questions about previous classifications that ascribe corundum from basalt-hosted gemfields to either “magmatic” or “metamorphic” sources. The spatial association of basalt-related gemfields in eastern Australia with a long-lived convergent margin suggests a link between corundum formation and Al-enrichment of the mantle wedge during periods of subduction.
Abstract: A wide number of genetic models have been proposed for volcanically transported ruby and sapphire deposits around the world. In this contribution we compare the trace element chemistry, mineral and melt inclusions, and oxygen isotope ratios in blue to reddish-violet sapphires from Yogo Gulch, Montana, U.S.A., with rubies from the Chantaburi-Trat region of Thailand and the Pailin region of Cambodia. The similarities between Thai/Cambodian rubies and Yogo sapphires suggest a common origin for gem corundum from both deposits. Specifically, we advance a model whereby sapphires and rubies formed through a peritectic melting reaction when the lamprophyre or basalts that transported the gem corundum to the surface partially melted Al-rich lower crustal rocks. Furthermore, we suggest the protolith of the rubies and sapphires was an anorthosite or, in the case of Thai/Cambodian rubies, an anorthosite subjected to higher pressures and converted into a garnet-clinopyroxenite. In this model the rubies and sapphires are rightfully considered to be xenocrysts in their host basalts or lamprophyre; however, in this scenario they are not "accidental" xenocrysts but their formation is intimately and directly linked to the magmas that transported them to the surface. The similarities in these gem corundum deposits suggests that the partial melting, non-accidental xenocryst model may be more wide-reaching and globally important than previously realized. Importantly, in both cases the gem corundum has an ostensibly "metamorphic" trace element signature, whereas the presence of silicate melt (or magma) inclusions shows they ought to be considered to be "magmatic" rubies and sapphires. This discrepancy suggests that existing trace element discriminant diagrams intended to separate "metamorphic" from "magmatic" gem corundum ought to be used with caution.
Mineralogical Magazine, Vol. 81, 6, pp. 1551-1576.
Australia, Tasmania
corundum classification
Abstract: Significant uncertainty surrounds the processes involved in the formation of basalt-hosted corundum, particularly the role that the mantle plays in corundum generation. Some previous studies have suggested that trace-element ratios (namely, Cr/Ga and Ga/Mg) are useful for distinguishing two types of corundum: ‘magmatic’ and ‘metamorphic’, designations that include mantle and crustal processes. However, recent studies, including this one, have discovered transitional groups between these end-members that are difficult to classify. We used laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) to measure trace-element concentrations in sapphire and ruby crystals from eight alluvial deposits that span a significant length of the eastern Australian gemstone belt. Additionally, we collected LA-ICP-MS U-Pb and trace-element data from zircon megacrysts at Weldborough, Tasmania, which is also within the gemstone belt. Our sapphire and ruby results reveal a continuum in trace-element compositions, an observation that raises questions regarding previous classifications that ascribe corundum from basalt-hosted gemfields to either ‘magmatic’ or ‘metamorphic’ sources. The spatial association of basalt-related gemfields in eastern Australia with a long-lived convergent margin suggests a link between corundum formation and Al-enrichment of the mantle wedge during periods of subduction.
Abstract: The question of whether high-grade metamorphism and crustal melting in the early Archaean were associated with modern-style plate tectonics is a major issue in unravelling early Earth crustal evolution, and the eastern Kaapvaal craton has featured prominently in this debate. We discuss a major ca. 3.2?Ga tectono-magmatic-metamorphic event in the Ancient Gneiss Complex (AGC) of Swaziland, a multiply deformed medium- to high-grade terrane in the eastern Kaapvaal craton consisting of 3.66-3.20?Ga granitoid gneisses and infolded greenstone remnants, metasedimentary assemblages and mafic dykes. We report on a 3.2?Ga granulite-facies assemblage in a metagabbro of the AGC of central Swaziland and relate this to a major thermo-magmatic event that not only affected the AGC but also the neighbouring Barberton granitoid-greenstone terrane. Some previous models have related the 3.2?Ga event in the eastern Kaapvaal craton to subduction processes, but we see no evidence for long, narrow belts and metamorphic facies changes reflecting lithospheric suture zones, and there is no unidirectional asymmetry in the thermal structure across the entire region from Swaziland to the southern Barberton granite-greenstone terrane as is typical of Phanerozoic and Proterozoic belts. Instead, we consider an underplating event at ca. 3.2?Ga, giving rise to melting in the lower crust and mixing with mantle-derived under- and intraplated mafic magma to generate the voluminous granitoid assemblages now observed in the AGC and the southern Barberton terrane. This is compatible with large-scale crustal reworking during a major thermo-magmatic event and the apparent lack of a mafic lower crust in the Kaapvaal craton as shown by seismic data.
Netherlands Journal of Geolsciences, Vol. 95, 4, pp. 491-522.
South America, Suriname
Guiana shield
Abstract: The Proterozoic basement of Suriname consists of a greenstone-tonalite-trondhjemite-granodiorite belt in the northeast of the country, two high-grade belts in the northwest and southwest, respectively, and a large granitoid-felsic volcanic terrain in the central part of the country, punctuated by numerous gabbroic intrusions. The basement is overlain by the subhorizontal Proterozoic Roraima sandstone formation and transected by two Proterozoic and one Jurassic dolerite dyke swarms. Late Proterozoic mylonitisation affected large parts of the basement. Almost 50 new U-Pb and Pb-Pb zircon ages and geochemical data have been obtained in Suriname, and much new data are also available from the neighbouring countries. This has led to a considerable revision of the geological evolution of the basement. The main orogenic event is the Trans-Amazonian Orogeny, resulting from southwards subduction and later collision between the Guiana Shield and the West African Craton. The first phase, between 2.18 and 2.09 Ga, shows ocean floor magmatism, volcanic arc development, sedimentation, metamorphism, anatexis and plutonism in the Marowijne Greenstone Belt and the adjacent older granites and gneisses. The second phase encompasses the evolution of the Bakhuis Granulite Belt and Coeroeni Gneiss Belt through rift-type basin formation, volcanism, sedimentation and, between 2.07 and 2.05 Ga, high-grade metamorphism. The third phase, between 1.99 and 1.95 Ga, is characterised by renewed high-grade metamorphism in the Bakhuis and Coeroeni belts along an anticlockwise cooling path, and ignimbritic volcanism and extensive and varied intrusive magmatism in the western half of the country. An alternative scenario is also discussed, implying an origin of the Coeroeni Gneiss Belt as an active continental margin, recording northwards subduction and finally collision between a magmatic arc in the south and an older northern continent. The Grenvillian collision between Laurentia and Amazonia around 1.2-1.0 Ga caused widespread mylonitisation and mica age resetting in the basement.
SAXI-XI Inter Guiana Geological Conferene 2019: Paramaribo, Suriname, 6p. Pdf
South America, Brazil, Venezuela
Guiana shield
Abstract: The Guiana Shield records a long history that starts in the Archean, but culminates in the Trans-Amazonian Orogeny between 2.26-2.09 Ga as a result of an Amazonian-West-Africa collision. This event is responsible for the emplacement of a major part of its mineralisations, especially gold, iron and manganese. The diamondiferous Roraima Supergroup represents its molasse. Between 1.86 and 1.72 Ga the Rio Negro Block accreted in the west. The Grenvillian Orogeny caused shearing and mineral resetting between 1.3 and 1.1 Ga when Amazonia collided with Laurentia. Younger platform covers contain placer gold mineralisation. Several suits of dolerite dykes record short-lived periods of crustal extension. Bauxite plateaus cover various rock units.
Abstract: When hot liquid metal drained towards the core during and shortly after Earth accretion, exceptional conditions may have led to the first global crystallisation of diamond. Newly reported metallic iron trapped in large mantle diamond invites comparison between commercial Fe-Ni-Co “HPHT” diamond growth and natural environments. We evaluate possible conditions for Hadean diamond crystallisation from liquid ironrich metal where thermal and compositional gradients influence diamond crystallization. The solubility of up to 6% carbon has little effect on the phase transitions of the metallic iron phase diagram and carbon generally decreases with increasing pressure in solid iron based on calculated enthalpies. Models for core differentiation provide two scenarios (i) from an accumulated metal “pond” (ii) from massive downward mobile metal diapirs. A refinement arises from a parameterization of self-propagating downward fractures filled by turbulent liquid iron as proposed by Stephenson to send a transponder to the core; negatively buoyant diamond crystals would float. Experiments show that diamond growth under these conditions is fast (~1 carat per hour) and micro-textures of natural diamond with metallic inclusions retain substantial isotopic heterogeneities. We speculate that if the oldest diamond trapped metallic iron on its way to form the core, such “stranded core” might be recognized by trace element compositions, and could retain anomalous isotopic signatures of W and Hf.
The Victor diamond mine, northern Ontario, Canada: successful mining of a reliable resource.
Proceedings of the 10th. International Kimberlite Conference, Vol. 2, Special Issue of the Journal of the Geological Society of India,, Vol. 2, pp. 19-33.
Abstract: Subduction of oceanic crust generates chemical and lithological heterogeneities in the mantle. An outstanding question is the extent to which these heterogeneities contribute to subsequent magmas generated by mantle melting, but the answer differs depending on the geochemical behaviour of the elements under investigation: analyses of incompatible elements (those that preferentially concentrate into silicate melts) suggest that recycled oceanic crust is an important contributor, whereas analyses of compatible elements (those that concentrate in crystalline residues) generally suggest it is not. Recently, however, the concentrations of Mn and Ni—two elements of varying compatibility—in early-crystallizing olivines, have been used to infer that erupted magmas are mixtures of partial melts of olivine-rich mantle rocks (that is, peridotite) and of metasomatic pyroxene-rich mantle rocks (that is, pyroxenite) formed by interaction between partial melts of recycled oceanic crust and peridotite. Here, we test whether melting of peridotite alone can explain the observed trend in olivine compositions by combining new experimental data on the partitioning of Mn between olivine and silicate melt under conditions relevant to basalt petrogenesis with earlier results on Ni partitioning. We show that the observed olivine compositions are consistent with melts of fertile peridotite at various pressures—importantly, melts from metasomatic pyroxenites are not required. Thus, although recycled materials may well be present in the mantle source regions of some basalts, the Mn and Ni data can be explained without such a contribution. Furthermore, the success of modelling the Mn–Ni contents of olivine phenocrysts as low-pressure crystallization products of partial melts of peridotite over a range of pressures implies a simple new approach for constraining depths of mantle melting.
Abstract: Diamond inclusions are the only samples from the mantle transition zone (410-660 km) and the lower mantle. Majoritic garnet is a rare inclusion, limited to pressures of ~8-20 Gpa with Si content being indicative of depth of re-equilibration. These garnet inclusions can therefore provide information on properties of the transition zone such as oxidation state. In this study, we used Synchrotron Mössbauer Source (SMS) to determine the ferric-ferrous ratios of 13 small (30 to 100 micrometers diameter) majoritic inclusions in diamonds from Jagersfontein. The studied inclusions have pyroxenitic affinities [1], with compositions intermediate between typical peridotite and eclogite. They contain 4.62-11.2 wt% CaO, 0.03-0.34 wt% Cr2O3 and Mg# of 0.65-0.81. Minimum pressures for their equilibration using Beyer and Frost [2] barometer are between 8 and 18 GPa with at least 4 of these inclusions being formed in the transition zone. The Fe3+/Fetotal ratios in the garnets increase from 0.08±0.01 to 0.30±0.03 with increasing pressure. These values define a clear extension of the trend apparent in the data from peridotite xenoliths crystallised at lower pressures. Thermodynamic calculations suggest that these high ferric contents correspond to oxygen fugacities above the FeFeO (IW) buffer, which means that the high Fe3+ contents were not generated by disproportionation of Fe2+ to Fe3+ and Fe0 . It is more likely that carbonate was the oxidising agent responsible for generating the high Fe3+ of these garnets.
Abstract: The oxidation state and oxygen fugacity (fO2) of Earth’s mantle exert important influences on the compositions of primary melts the speciation and mobility of carbon and sulphur, diamond formation, and the modification of subducted lithosphere [1, 2] It is generally observed that the oxygen fugacity of both cratonic and asthenospheric mantle is close to FMQ in the spinel field and that fO2 in the cratons generally decreases with depth. According to experimental studies combined with thermodynamic modelling, at depths below 180-200 km the decreasing oxygen fugacity should destabilise carbonate with all carbon at greater depths being stored as diamond [1, 3]. These pressure effects also tend to stabilise metal in the transition zone following the disproportionation of divalent iron (FeO) into Fe (metal) and Fe3+ (accommodated in garnet) [4]. To date, inclusions in diamond are the only available samples from the mantle transition zone and the lower mantle and these provide the opportunity for study of redox relationships in the deep mantle. In this study we used synchrotron Mössbauer Spectroscopy to measure Fe3+/(Fe2++ Fe3+) ratios of majoritic inclusions in diamonds from the lowermost upper mantle and the mantle transition zone for comparison with garnets from the shallow mantle. We find that there is a systematic increase with depth of the oxidation state of iron in garnets included in diamonds, with the deepest samples (~550 km depth) having Fe3+/(Fe2++ Fe3+) of up to 0.30, which is more than twice as great as in non-majoritic upper mantle garnets (< 200 km depth) [5]. When converted to oxygen fugacity these measurements imply conditions just above the stability field of metallic iron (above IW).
Abstract: The oxidation state of iron in Earth’s mantle is well known to depths of approximately 200?km, but has not been characterized in samples from the lowermost upper mantle (200-410?km depth) or the transition zone (410-660?km depth). Natural samples from the deep (>200?km) mantle are extremely rare, and are usually only found as inclusions in diamonds. Here we use synchrotron Mössbauer source spectroscopy complemented by single-crystal X-ray diffraction to measure the oxidation state of Fe in inclusions of ultra-high pressure majoritic garnet in diamond. The garnets show a pronounced increase in oxidation state with depth, with Fe3+/(Fe3++ Fe2+) increasing from 0.08 at approximately 240?km depth to 0.30 at approximately 500?km depth. The latter majorites, which come from pyroxenitic bulk compositions, are twice as rich in Fe3+ as the most oxidized garnets from the shallow mantle. Corresponding oxygen fugacities are above the upper stability limit of Fe metal. This implies that the increase in oxidation state is unconnected to disproportionation of Fe2+ to Fe3+ plus Fe0. Instead, the Fe3+ increase with depth is consistent with the hypothesis that carbonated fluids or melts are the oxidizing agents responsible for the high Fe3+ contents of the inclusions.
Abstract: Synchrotron Mössbauer Source (SMS) spectroscopy (ESRF, Grenoble, France) has high spatial resolution (~20 microns) and has been successfully applied to measuring Fe3+ concentrations in diamond inclusions [1,2]. Over the last few decades a number of studies have been conducted on individual minerals from mantle xenoliths in order to determine the oxidation state of the upper mantle [3,4]. These studies were conducted using ?50 mg of handpicked grains as opposed to individual crystals. In this study, we applied SMS to measure ferric iron contents of individual spinels, orthopyroxenes, clinopyroxenes and garnets from 5 spinel peridotite xenoliths and 1 pyroxenite and 2 eclogite xenoliths. Spinel xenoliths derive from Kilbourne hole, Mont Briançon and Ichinomegata. Spinels from these xenoliths were previously analysed by Mössbauer spectroscopy on bulk separates [4]. Eclogite xenoliths (UAS 1055, UAS 1525) and pyroxenite xenolith (UAS 510) were obtained from Udachnaya kimberlite pipe in Siberia. In spinel peridotites measured ratios range between 0.04- 0.14 Fe3+/Fetot for Opx, 0.14-0.19 Fe3+/Fetot for Cpx and between 0.15-0.23 for Spl. These values are broadly in agreement with previous measurements [3]. In eclogites and pyroxenite, the ratios range between 0.05-0.16 for garnet and 0.07-0.17 for Cpx, showing DGrt/Cpx for Fe3+ of 0.8-1.9. Oxygen fugacities derived from the spinel-olivineorthopyroxene oxybarometer are consistent with previous results for the continental lithosphere fO2 of between -1 and +1 log units relative to the FMQ buffer [5]. Nevertheless we observe small differences between our results on individual grains and previous data on bulk separates.
geochemicalperspectives.org, Vol. 6, 1, April, 187p. Pdf 28 MB
Global
geochemistry
Abstract: Some scientists and journalists, and many members of the general public, have been led to believe that the world is rapidly running out of the metals on which our modern society is based. Advocates of the peak metal concept have predicted for many decades that increasing consumption will soon lead to exhaustion of mineral resources. Yet, despite ever-increasing production and consumption, supplies of minerals have continued to meet the needs of industry and society, and lifetimes of reserves remain similar to what they were 30-40 years ago. In this volume, we discuss the reasons for this apparent paradox using our broad experience and expertise on both academic and industrial sides of the minerals sector. Many misconceptions arise from flawed estimates of the size of global mineral resources which stem from a lack of understanding of the critical difference between reserves and resources. Some authors use quoted reserves – the amount of metal proven to exist and to be economic for mining at present – when predicting imminent shortages. Resources – the amount that may be accessible in the upper few kilometres of the crust – are far larger.Over the last 150 years, improved technologies, economies of scale and increased efficiency have combined to reduce costs hence allowing lower-grade ore to be mined economically. The net result is that the long-term inflation-adjusted price of most metals has decreased more or less in parallel with increasing production, a second apparent paradox that frequently is not well understood. Using copper as the principal example and other metals as appropriate, we summarise the latest research on ore deposits and the activities of the minerals industry. Following a description of the numerous geological processes that form ore deposits, we outline the scientific methods used by the minerals industry to explore for new deposits. We also discuss how resources are mined and how minerals are processed, as well as recent efforts to reduce related environmental impacts. Economic and societal factors influence supply, and these are as important as the actual presence of a resource. Finally, we discuss the critical roles that geoscientists will play in assuring continued supplies of minerals. These include the development of new concepts and techniques that will assist the discovery, mining, processing, remediation, and management of mineral resources. It is essential that researchers help to educate the general public about the need for continued exploration to find new resources to meet growth in world living standards. We demonstrate that global resources of copper, and probably of most other metals, are much larger than most currently available estimates, especially if increasing efficiencies and higher prices allow lower-grade ores to be mined. These observations indicate that supplies of important mineral commodities will remain adequate for the foreseeable future.
Journal of Volcanology and Geothermal Research, Vol. 354, pp. 87-101.
Mantle
magmatism
Abstract: Volcanic eruptions are fed by plumbing systems that transport magma from its source to the surface, mostly fed by dykes. Here we present laboratory experiments that model dyke ascent to eruption using a tank filled with a crust analogue (gelatine, which is transparent and elastic) that is injected from below by a magma analogue (dyed water). This novel experimental setup allows, for the first time, the simultaneous measurement of fluid flow, sub-surface and surface deformation during dyke ascent. During injection, a penny-shaped fluid-filled crack is formed, intrudes, and traverses the gelatine slab vertically to then erupt at the surface. Polarised light shows the internal stress evolution as the dyke ascends, and an overhead laser scanner measures the surface elevation change in the lead-up to dyke eruption. Fluorescent passive-tracer particles that are illuminated by a laser sheet are monitored, and the intruding fluid's flow dynamics and gelatine's sub-surface strain evolution is measured using particle image velocimetry and digital image correlation, respectively. We identify 4 previously undescribed stages of dyke ascent. Stage 1, early dyke growth: the initial dyke grows from the source, and two fluid jets circulate as the penny-shaped crack is formed. Stage 2, pseudo-steady dyke growth: characterised by the development of a rapidly uprising, central, single pseudo-steady fluid jet, as the dyke grows equally in length and width, and the fluid down-wells at the dyke margin. Sub-surface host strain is localised at the head region and the tail of the dyke is largely static. Stage 3, pre-eruption unsteady dyke growth: an instability in the fluid flow appears as the central fluid jet meanders, the dyke tip accelerates towards the surface and the tail thins. Surface deformation is only detected in the immediate lead-up to eruption and is characterised by an overall topographic increase, with axis-symmetric topographic highs developed above the dyke tip. Stage 4 is the onset of eruption, when fluid flow is projected outwards and focused towards the erupting fissure as the dyke closes. A simultaneous and abrupt decrease in sub-surface strain occurs as the fluid pressure is released. Our results provide a comprehensive physical framework upon which to interpret evidence of dyke ascent in nature, and suggest dyke ascent models need to be re-evaluated to account for coupled intrusive and extrusive processes and improve the recognition of monitoring signals that lead to volcanic eruptions in nature.
Howell, D., Piazolo, S., Dobson, D.P., Wood, I.G., Jones, A.P., Watte, N., Frost, D.J., Fisher, D., Griffin, W.L.
Quantitative characterization of plastic deformation of single diamond crystals: a high pressure high temperature (HPHT) experimental deformation study combines with electron backscatter diffraction.
Diamond and Related Materials, Vol. 30, pp. 20-30.
Abstract: Seismology records the presence of various heterogeneities throughout the lower mantle1,2, but the origins of these signals—whether thermal or chemical—remain uncertain, and therefore much of the information that they hold about the nature of the deep Earth is obscured. Accurate interpretation of observed seismic velocities requires knowledge of the seismic properties of all of Earth’s possible mineral components. Calcium silicate (CaSiO3) perovskite is believed to be the third most abundant mineral throughout the lower mantle. Here we simultaneously measure the crystal structure and the shear-wave and compressional-wave velocities of samples of CaSiO3 perovskite, and provide direct constraints on the adiabatic bulk and shear moduli of this material. We observe that incorporation of titanium into CaSiO3 perovskite stabilizes the tetragonal structure at higher temperatures, and that the material’s shear modulus is substantially lower than is predicted by computations3,4,5 or thermodynamic datasets6. When combined with literature data and extrapolated, our results suggest that subducted oceanic crust will be visible as low-seismic-velocity anomalies throughout the lower mantle. In particular, we show that large low-shear-velocity provinces (LLSVPs) are consistent with moderate enrichment of recycled oceanic crust, and mid-mantle discontinuities can be explained by a tetragonal-cubic phase transition in Ti-bearing CaSiO3 perovskite.
Abstract: Diamonds are a valuable tool for petrologists in order to study the lithospheric mantle. Diamond’s unique material properties enable it to act as a record of the conditions within the mantle from which diamonds grow, through mineral inclusions and crystallographic defects within the lattice. One impurity often observed is hydrogen, with the most common form being the N3VH centre, seen in the IR spectra of many natural diamonds. Despite its ubiquity, it is not well understood. This work initially presents an attempt at quantification of the amount of hydrogen present in natural diamonds and how it relates to the amount of N3VH. The results suggest that most hydrogen within diamonds is not contained in the N3VH defect, with the concentrations observed over 20 times higher than predicted using IR alone. High-quality IR and UV-vis line scans are then used to interrogate the effect of hydrogen on the nitrogen aggregation sequence in diamonds, specifically using the concentration of N3, a minor aggregate. This enables generation of proportionality constants within each diamond and suggests that the primary formation mechanism of N3VH is through direct protonation of N3. A methodology is laid out for studying the availability of hydrogen within diamond-forming fluids through the study of the relative abundance of N3 and N3VH within a diamond. A minor IR peak at 3236 cm-1 is also investigated through comparison with other IR features, and some evidence is found for aggregated nitrogen and platelets in the defect structure.
Nature Research Scientific Reports, Vol. 9:20190 doir.org/10.38 /s41598-019-55743-1, 11p. Pdf
Mantle
eclogite
Abstract: Oxygen fugacity (ƒO2) is an intensive variable implicated in a range of processes that have shaped the Earth system, but there is controversy on the timing and rate of oxidation of the uppermost convecting mantle to its present ƒO2 around the fayalite-magnetite-quartz oxygen buffer. Here, we report Fe3+/?Fe and ƒO2 for ancient eclogite xenoliths with oceanic crustal protoliths that sampled the coeval ambient convecting mantle. Using new and published data, we demonstrate that in these eclogites, two redox proxies, V/Sc and Fe3+/?Fe, behave sympathetically, despite different responses of their protoliths to differentiation and post-formation degassing, seawater alteration, devolatilisation and partial melting, testifying to an unexpected robustness of Fe3+/?Fe. Therefore, these processes, while causing significant scatter, did not completely obliterate the underlying convecting mantle signal. Considering only unmetasomatised samples with non-cumulate and little-differentiated protoliths, V/Sc and Fe3+/?Fe in two Archaean eclogite suites are significantly lower than those of modern mid-ocean ridge basalts (MORB), while a third suite has ratios similar to modern MORB, indicating redox heterogeneity. Another major finding is the predominantly low though variable estimated ƒO2 of eclogite at mantle depths, which does not permit stabilisation of CO2-dominated fluids or pure carbonatite melts. Conversely, low-ƒO2 eclogite may have caused efficient reduction of CO2 in fluids and melts generated in other portions of ancient subducting slabs, consistent with eclogitic diamond formation ages, the disproportionate frequency of eclogitic diamonds relative to the subordinate abundance of eclogite in the mantle lithosphere and the general absence of carbonate in mantle eclogite. This indicates carbon recycling at least to depths of diamond stability and may have represented a significant pathway for carbon ingassing through time.
Marine diamonds: the geological controls governing the marine and terrestrial diamond deposits occurring along the West Coast of the Republic of South Africa
Indiaqua, Industrial Diamond ANNUAL, 1991 pp. 53-56, 58-59
New Strontium, neodymium, lead isotopic dat a from plutons in the northern Great Basin: implications for crustal structure and granite petrogenesis in the hinterland of the Sevier th
Proterozoic evolution of the western margin of the Wyoming Craton: implications for the tectonic and magmatic evolution of the northern Rocky Mountains.
Canadian Journal of Earth Sciences, Vol. 43, 10, pp. 1601-1619,
Kent, A.J.R., Stolper, E.M., Francis, D., Woodhead, J., Frei, R., Eiler, J.
Mantle heterogeneity during the formation of the North Atlantic igneous province: constraints from trace element and Sr Nd Os O isotope - Baffin Island picrites
Geochemistry, Geophysics, Geosystems: G3, Vol. 5, pp. Q11004 10.1029/2004GC000743
Abstract: The lack of consensus on the possible range of initial kimberlite melt compositions and their evolution as they ascend through and interact with mantle and crustal wall rocks, hampers a complete understanding of kimberlite petrogenesis. Attempts to resolve these issues are complicated by the fact that kimberlite rocks are mixtures of magmatic, xenocrystic and antecrystic components and, hence, are not directly representative of their parental melt composition. Furthermore, there is a lack of direct evidence of the assimilation processes that may characterise kimberlitic melts during ascent, which makes understanding their melt evolution difficult. In this contribution we provide novel constraints on the interaction between precursor kimberlite melts and lithospheric mantle wall rocks. We present detailed textural and geochemical data for a carbonate-rich vein assemblage that traverses a garnet wehrlite xenolith [equilibrated at ~ 1060 °C and 43 kbar (~ 140-145 km)] from the Bultfontein kimberlite (Kimberley, South Africa). This vein assemblage is dominated by Ca-Mg carbonates, with subordinate oxide minerals, olivine, sulphides, and apatite. Vein phases have highly variable compositions indicating formation under disequilibrium conditions. Primary inclusions in the vein minerals and secondary inclusion trails in host wehrlite minerals contain abundant alkali-bearing phases (e.g., Na-K bearing carbonates, Mg-freudenbergite, Na-bearing apatite and phlogopite). The Sr-isotope composition of vein carbonates overlaps those of groundmass calcite from the Bultfontein kimberlite, as well as perovskite from the other kimberlites in the Kimberley area. Clinopyroxene and garnet in the host wehrlite are resorbed and have Si-rich reaction mantles where in contact with the carbonate-rich veins. Within some veins, the carbonates occur as droplet-like, globular segregations, separated from a similarly shaped Si-rich phase by a thin meniscus of Mg-magnetite. These textures are interpreted to represent immiscibility between carbonate and silicate melts. The preservation of reaction mantles, immiscibility textures and disequilibrium in the vein assemblage, suggests quenching, probably triggered by entrainment and rapid transport toward the Earth's surface in the host kimberlite magma. Based on the Sr-isotope systematics of vein carbonate minerals, and the close temporal relationship between carbonate-rich metasomatism and kimberlite magmatism, we suggest that the carbonate-rich vein assemblage was produced by the interaction between a melt genetically related to the Bultfontein kimberlite and wehrlitic mantle wall rock. If correct, this unique xenolith sample provides a rare snapshot of the assimilation processes that might characterise parental kimberlite melts during their ascent through the lithospheric mantle.
Abstract: Magmas forming large igneous provinces (LIP) on continents are generated by extensive melting in the deep crust and underlying mantle and associated with break-up of ancient supercontinents, followed by formation of a new basaltic crust in the mid-oceanic rifts. A lack of the unifying model in understanding the sources of LIP magmatism is justified by lithological and geochemical complexity of erupted magmas on local (e.g. a cross-section) and regional (a single and different LIP) scales. Moreover, the majority of LIP rocks do not fit general criteria for recognizing primary/primitive melts (i.e. < 8 wt% MgO and absence of high-Fo olivine phenocrysts). This study presents the mineralogical (olivine, Cr-spinel, orthopyroxene), geochemical (trace elements and Sr-Nd-Hf-Pb isotopes) and olivine-hosted melt inclusion compositional characteristics of a single primitive (16 wt% MgO), high-Ti (2.5 wt% TiO2) picrite with high-Mg olivine (up to 91 mol% Fo) from the Letaba Formation in the ~ 180 Ma Karoo LIP (south Africa). The olivine compositions (unusually high ?18O (6.17‰), high NiO (0.36-0.56 wt%) and low MnO and CaO (0.12-0.20 and 0.12-0.22 wt%, respectively)) are used to argue for a non-peridotitic mantle source. This is supported by the enrichment of the rock and melts in most incompatible trace elements and depletion in heavy rare earth elements (e.g. high Gd/Yb) that reflects residual garnet in the source of melting. The radiogenic isotopes resemble those of the model enriched mantle (EM-1) and further argue for a long-term enrichment of the source in incompatible trace elements. The enriched high-Ti compositions, strongly fractionated incompatible trace elements, presence of primitive olivine and high-Cr spinel in the Letaba picrites are closely matched by olivine-phyric rocks from the ~ 260 Ma Emeishan (Yongsheng area, SW China) and ~ 250 Ma Siberian (Maimecha-Kotuy region, N Siberia) LIPs. However, many other compositional parameters (e.g. trace element and ?18O compositions of olivine phenocrysts, Fe2 +/Fe3 + in Cr-spinel, Sr-Nd-Hf isotope ratios) only partially overlap or even diverge. We thus imply that parental melts of enriched picritic rocks with forsteritic olivine from three major continental igneous provinces - Karoo, Emeishan and Siberia cannot be assigned to a common mantle source and similar melting conditions. The Karoo picrites also exhibit some mineralogical and geochemical similarities with rocks and glasses in the south Atlantic Ridge and adjacent fracture zones. The geodynamic reconstructions of the continental plate motions since break-up of the Gondwanaland in the Jurassic support the current position of the source of the Karoo magmatism in the southernmost Atlantic. Co-occurrence of modern and recent anomalous rocks with normal mid-ocean ridge basalts in this region can be related to blocks/rafts of the ancient lithosphere, stranded in the ambient upper mantle and occasionally sampled by rifting-related decompressional melting.
Abstract: Magmas forming large igneous provinces (LIP) on continents are generated by extensive melting in the deep crust and underlying mantle and associated with break-up of ancient supercontinents, followed by formation of a new basaltic crust in the mid-oceanic rifts. A lack of the unifying model in understanding the sources of LIP magmatism is justified by lithological and geochemical complexity of erupted magmas on local (e.g. a cross-section) and regional (a single and different LIP) scales. Moreover, the majority of LIP rocks do not fit general criteria for recognizing primary/primitive melts (i.e. < 8 wt% MgO and absence of high-Fo olivine phenocrysts). This study presents the mineralogical (olivine, Cr-spinel, orthopyroxene), geochemical (trace elements and Sr-Nd-Hf-Pb isotopes) and olivine-hosted melt inclusion compositional characteristics of a single primitive (16 wt% MgO), high-Ti (2.5 wt% TiO2) picrite with high-Mg olivine (up to 91 mol% Fo) from the Letaba Formation in the ~ 180 Ma Karoo LIP (south Africa). The olivine compositions (unusually high ?18O (6.17‰), high NiO (0.36–0.56 wt%) and low MnO and CaO (0.12–0.20 and 0.12–0.22 wt%, respectively)) are used to argue for a non-peridotitic mantle source. This is supported by the enrichment of the rock and melts in most incompatible trace elements and depletion in heavy rare earth elements (e.g. high Gd/Yb) that reflects residual garnet in the source of melting. The radiogenic isotopes resemble those of the model enriched mantle (EM-1) and further argue for a long-term enrichment of the source in incompatible trace elements. The enriched high-Ti compositions, strongly fractionated incompatible trace elements, presence of primitive olivine and high-Cr spinel in the Letaba picrites are closely matched by olivine-phyric rocks from the ~ 260 Ma Emeishan (Yongsheng area, SW China) and ~ 250 Ma Siberian (Maimecha-Kotuy region, N Siberia) LIPs. However, many other compositional parameters (e.g. trace element and ?18O compositions of olivine phenocrysts, Fe2 +/Fe3 + in Cr-spinel, Sr-Nd-Hf isotope ratios) only partially overlap or even diverge. We thus imply that parental melts of enriched picritic rocks with forsteritic olivine from three major continental igneous provinces – Karoo, Emeishan and Siberia cannot be assigned to a common mantle source and similar melting conditions. The Karoo picrites also exhibit some mineralogical and geochemical similarities with rocks and glasses in the south Atlantic Ridge and adjacent fracture zones. The geodynamic reconstructions of the continental plate motions since break-up of the Gondwanaland in the Jurassic support the current position of the source of the Karoo magmatism in the southernmost Atlantic. Co-occurrence of modern and recent anomalous rocks with normal mid-ocean ridge basalts in this region can be related to blocks/rafts of the ancient lithosphere, stranded in the ambient upper mantle and occasionally sampled by rifting-related decompressional melting.
Geochemical Perspectives Letters, Vol. 4, pp. 1-6.
Africa, South Africa, Zimbabwe
metasomatism, geochronology
Abstract: Metasomatism, the chemical alteration of rocks by a variety of melts and fluids, has formed a key concept in studies of the Earth’s mantle for decades. Metasomatic effects are often inferred to be far-reaching and yet the evidence for their occurrence is usually based upon individual hand specimens or suites of rocks that display considerable heterogeneity. In rare cases, however, we are offered insights into larger-scale chemical modifications that occur in the mantle. Here we utilise the Lu–Hf systematics of zircon megacrysts erupted in kimberlite magmas to discern two temporally and compositionally discrete metasomatic events in the mantle beneath southern Africa, each having an influence extending over an area exceeding one million km2. These data provide unambiguous evidence for metasomatic processes operating at continental scales and seemingly unperturbed by the age and composition of the local lithospheric mantle. The most recent of these events may be associated with the major Jurassic-Karoo magmatism in southern Africa.
Abstract: Metasomatism, the chemical alteration of rocks by a variety of melts and fluids, has formed a key concept in studies of the Earth’s mantle for decades. Metasomatic effects are often inferred to be far-reaching and yet the evidence for their occurrence is usually based upon individual hand specimens or suites of rocks that display considerable heterogeneity. In rare cases, however, we are offered insights into larger-scale chemical modifications that occur in the mantle. Here we utilise the Lu–Hf systematics of zircon megacrysts erupted in kimberlite magmas to discern two temporally and compositionally discrete metasomatic events in the mantle beneath southern Africa, each having an influence extending over an area exceeding one million km2. These data provide unambiguous evidence for metasomatic processes operating at continental scales and seemingly unperturbed by the age and composition of the local lithospheric mantle. The most recent of these events may be associated with the major Jurassic-Karoo magmatism in southern Africa.
Abstract: The widely accepted paradigm of Earth's geochemical evolution states that the successive extraction of melts from the mantle over the past 4.5 billion years formed the continental crust, and produced at least one complementary melt-depleted reservoir that is now recognized as the upper-mantle source of mid-ocean-ridge basalts1. However, geochemical modelling and the occurrence of high 3He/4He (that is, primordial) signatures in some volcanic rocks suggest that volumes of relatively undifferentiated mantle may reside in deeper, isolated regions2. Some basalts from large igneous provinces may provide temporally restricted glimpses of the most primitive parts of the mantle3,4, but key questions regarding the longevity of such sources on planetary timescales—and whether any survive today—remain unresolved. Kimberlites, small-volume volcanic rocks that are the source of most diamonds, offer rare insights into aspects of the composition of the Earth’s deep mantle. The radiogenic isotope ratios of kimberlites of different ages enable us to map the evolution of this domain through time. Here we show that globally distributed kimberlites originate from a single homogeneous reservoir with an isotopic composition that is indicative of a uniform and pristine mantle source, which evolved in isolation over at least 2.5 billion years of Earth history—to our knowledge, the only such reservoir that has been identified to date. Around 200 million years ago, extensive volumes of the same source were perturbed, probably as a result of contamination by exogenic material. The distribution of affected kimberlites suggests that this event may be related to subduction along the margin of the Pangaea supercontinent. These results reveal a long-lived and globally extensive mantle reservoir that underwent subsequent disruption, possibly heralding a marked change to large-scale mantle-mixing regimes. These processes may explain why uncontaminated primordial mantle is so difficult to identify in recent mantle-derived melts.
Abstract: The widely accepted paradigm of Earth's geochemical evolution states that the successive extraction of melts from the mantle over the past 4.5 billion years formed the continental crust, and produced at least one complementary melt-depleted reservoir that is now recognized as the upper-mantle source of mid-ocean-ridge basalts1. However, geochemical modelling and the occurrence of high 3He/4He (that is, primordial) signatures in some volcanic rocks suggest that volumes of relatively undifferentiated mantle may reside in deeper, isolated regions2. Some basalts from large igneous provinces may provide temporally restricted glimpses of the most primitive parts of the mantle3,4, but key questions regarding the longevity of such sources on planetary timescales—and whether any survive today—remain unresolved. Kimberlites, small-volume volcanic rocks that are the source of most diamonds, offer rare insights into aspects of the composition of the Earth’s deep mantle. The radiogenic isotope ratios of kimberlites of different ages enable us to map the evolution of this domain through time. Here we show that globally distributed kimberlites originate from a single homogeneous reservoir with an isotopic composition that is indicative of a uniform and pristine mantle source, which evolved in isolation over at least 2.5 billion years of Earth history—to our knowledge, the only such reservoir that has been identified to date. Around 200 million years ago, extensive volumes of the same source were perturbed, probably as a result of contamination by exogenic material. The distribution of affected kimberlites suggests that this event may be related to subduction along the margin of the Pangaea supercontinent. These results reveal a long-lived and globally extensive mantle reservoir that underwent subsequent disruption, possibly heralding a marked change to large-scale mantle-mixing regimes. These processes may explain why uncontaminated primordial mantle is so difficult to identify in recent mantle-derived melts.
Abstract: The Karelian Craton in Finland is host to (at least) two distinct pulses of kimberlite magmatism. Twenty kimberlite occurrences have so far been discovered on the southwest margin of the craton at Kaavi-Kuopio and seven kimberlites are located in the Kuusamo area within the core of the craton. Comprehensive radiometric age determinations (U-Pb, Ar- Ar and Rb-Sr) reveal that all kimberlite activity was restricted to the Proterozoic. The Kaavi-Kuopio field was emplaced over a protracted period from ~610 to 550 Ma and is predated by the Kuusamo cluster that represents a relatively short pulse of magmatism at ~750 to 730 Ma. The emplacement of kimberlites globally has recently been linked to supercontinent reorganisation and we propose a similar scenario for these Finnish occurrences which, at the time of kimberlite emplacement, were situated on the Baltica paleo-continent. This land mass was contiguous with Laurentia in the Proterozoic and together formed part of Rodinia. The breakup of Rodinia is considered to have commenced at ~750 Ma and initiation of the opening of the Iapetus ocean at ~615 Ma. Contemporaneous with Kaavi-Kuopio magmatism, this latter period of Neoproterozoic crustal extension also includes the emplacement of kimberlites and related rocks in areas that were linked with Baltica as part of Rodinia - West Greenland and eastern North America. Both the initial and final periods of Rodinia’s breakup have been linked to mantle upwellings from the core-mantle boundary. We suggest that kimberlite magmatism in Finland was promoted by the influx of heat from mantle upwellings and lithospheric extension associated with the demise of Rodinia. Although both magmatic episodes are potentially linked to the breakup of Rodinia, whole-rock and perovskite radiogenic isotope compositions for the Kuusamo kimberlites (?Nd(i) +2.6 to +3.3, ?Hf(i) +3.1 to +5.6) are distinct from the Kaavi-Kuopio kimberlites (?Nd(i) -0.7 to +1.8, ?Hf(i) -6.1 to +5.2). The spread in Hf isotope compositions for the Kaavi-Kuopio magmas may be linked to variable assimilation of diverse mantle lithologies.
PNAS, Vol. 118, no. 23, doi.org/10.1073/pnas .e2020680118 8p. Pdf
Mantle
deep source, genesis
Abstract: Globally distributed kimberlites with broadly chondritic initial 143Nd-176Hf isotopic systematics may be derived from a chemically homogenous, relatively primitive mantle source that remained isolated from the convecting mantle for much of the Earth’s history. To assess whether this putative reservoir may have preserved remnants of an early Earth process, we report 182W/184W and 142Nd/144Nd data for "primitive" kimberlites from 10 localities worldwide, ranging in age from 1,153 to 89 Ma. Most are characterized by homogeneous ?182W and ?142Nd values averaging ?5.9 ± 3.6 ppm (2SD, n = 13) and +2.7 ± 2.9 ppm (2SD, n = 6), respectively. The remarkably uniform yet modestly negative ?182W values, coupled with chondritic to slightly suprachondritic initial 143Nd/144Nd and 176Hf/177Hf ratios over a span of nearly 1,000 Mya, provides permissive evidence that these kimberlites were derived from one or more long-lived, early formed mantle reservoirs. Possible causes for negative ?182W values among these kimberlites include the transfer of W with low ?182W from the core to the mantle source reservoir(s), creation of the source reservoir(s) as a result of early silicate fractionation, or an overabundance of late-accreted materials in the source reservoir(s). By contrast, two younger kimberlites emplaced at 72 and 52 Ma and characterized by distinctly subchondritic initial 176Hf/177Hf and 143Nd/144Nd have ?182W values consistent with the modern upper mantle. These isotopic compositions may reflect contamination of the ancient kimberlite source by recycled crustal components with ?182W ? 0.
Abstract: The petrogenesis of kimberlites commonly is obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during overprinting by such fluids and on the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa).
Abstract: The petrogenesis of kimberlites is commonly obscured by interaction with hydrothermal fluids, including deuteric (late-magmatic) and/or groundwater components. To provide new constraints on the modification of kimberlite rocks during fluid interaction and the fractionation of kimberlite magmas during crystallisation, we have undertaken a detailed petrographic and geochemical study of a hypabyssal sample (BK) from the Bultfontein kimberlite (Kimberley, South Africa). Sample BK consists of abundant macrocrysts (> 1 mm) and (micro-) phenocrysts of olivine and lesser phlogopite, smaller grains of apatite, serpentinised monticellite, spinel, perovskite, phlogopite and ilmenite in a matrix of calcite, serpentine and dolomite. As in kimberlites worldwide, BK olivine grains consist of cores with variable Mg/Fe ratios, overgrown by rims that host inclusions of groundmass phases (spinel, perovskite, phlogopite) and have constant Mg/Fe, but variable Ni, Mn and Ca concentrations. Primary multiphase inclusions in the outer rims of olivine and in Fe-Ti-rich (‘MUM’) spinel are dominated by dolomite, calcite and alkali carbonates with lesser silicate and oxide minerals. Secondary inclusions in olivine host an assemblage of Na-K carbonates and chlorides. The primary inclusions are interpreted as crystallised alkali-Si-bearing Ca-Mg-rich carbonate melts, whereas secondary inclusions host Na-K-rich C-O-H-Cl fluids. In situ Sr-isotope analyses of groundmass calcite and perovskite reveal similar 87Sr/86Sr ratios to perovskite in the Bultfontein and the other Kimberley kimberlites, i.e. magmatic values. The ?18O composition of the BK bulk carbonate fraction is above the mantle range, whereas the ?13C values are similar to those of mantle-derived magmas. The occurrence of different generations of serpentine and occasional groundmass calcite with high 87Sr/86Sr, and elevated bulk carbonate ?18O values indicate that the kimberlite was overprinted by hydrothermal fluids, which probably included a significant groundwater component. Before this alteration the groundmass included calcite, monticellite, apatite and minor dolomite, phlogopite, spinel, perovskite and ilmenite. Inclusions of groundmass minerals in olivine rims and phlogopite phenocrysts show that olivine and phlogopite also belong to the magmatic assemblage. We therefore suggest that the crystallised kimberlite was produced by an alkali-bearing, phosphorus-rich, silica-dolomitic melt. The alkali-Si-bearing Ca-Mg-rich carbonate compositions of primary melt inclusions in the outer rims of olivine and in spinel grains with evolved compositions (MUM spinel) support formation of these melts after fractionation of abundant olivine, and probably other phases (e.g., ilmenite and chromite). Finally, the similarity between secondary inclusions in kimberlite olivine of this and other worldwide kimberlites and secondary inclusions in minerals of carbonatitic, mafic and felsic magmatic rocks, suggests trapping of residual Na-K-rich C-O-H-Cl fluids after groundmass crystallisation. These residual fluids may have persisted in pore spaces within the largely crystalline BK groundmass and subsequently mixed with larger volumes of external fluids, which triggered serpentine formation and localised carbonate recrystallisation.
Earth and Planetary Science Letters, Vol. 401, pp. 132-147.
Africa, South Africa
metasomatism
Abstract: The Karoo igneous rocks (174-185 Ma) of southern Africa represent one of the largest continental flood basalt provinces on Earth. Available evidence indicates that Karoo magmas either originated in the asthenosphere and were extensively modified by interaction with the lithospheric mantle prior to emplacement in the upper crust; or were produced by partial melting of enriched mantle lithosphere. However, no direct evidence of interaction by Karoo melts (or their precursors) with lithospheric mantle rocks has yet been identified in the suites of mantle xenoliths sampled by post-Karoo kimberlites in southern Africa. Here we report U-Pb ages for lindsleyite-mathiasite (LIMA) titanate minerals (crichtonite series) from three metasomatised, phlogopite and clinopyroxene-rich peridotite xenoliths from the ?84 Ma Bultfontein kimberlite (Kimberley, South Africa), located in the southern part of the Karoo magmatic province. The LIMA minerals appear to have formed during metasomatism of the lithospheric mantle by fluids enriched in HFSE (Ti, Zr, Hf, Nb), LILE (K, Ba, Ca, Sr) and LREE. LIMA U-Pb elemental and isotopic compositions were measured in situ by LA-ICP-MS methods, and potential matrix effects were evaluated by solution-mode analysis of mineral separates. LIMA minerals from the three samples yielded apparent U-Pb ages of , and (). A single zircon grain extracted from the ?190 Ma LIMA-bearing sample produced a similar U-Pb age of , within uncertainty of the LIMA ages. These data provide the first robust evidence of fluid enrichment in the lithospheric mantle beneath the Kimberley region at ?180-190 Ma, and suggest causation of mantle metasomatism by Karoo melts or their precursor(s). The results further indicate that U-Pb dating of LIMA minerals provides a new, accurate tool for dating metasomatic events in the lithospheric mantle.
Earth and Planetary Science Letters, Vol. 482, pp. 253-264.
Africa, South Africa
metasomatism
Abstract: Radiogenic isotope variations unrelated to radiogenic ingrowth are common between minerals found in metasomatised mantle xenoliths entrained in kimberlite, basalts and related magmas. As the metasomatic minerals are assumed to have been in isotopic equilibrium originally, such variations are typically attributed to contamination by the magma host and/or interaction with mantle fluids during or before xenolith transport to surface. However, the increasing evidence of metasomatism by multiple, compositionally distinct fluids permeating the lithospheric mantle, coeval with specific magmatic events, suggests that isotopic disequilibrium might be a consequence of discrete, though complex, metasomatic events. Here we provide clear evidence of elemental and Sr isotope heterogeneity between coeval Ti-rich LIMA (lindsleyite–mathiasite) minerals at the time of their formation in the mantle. LIMA minerals occur in close textural association with clinopyroxene and phlogopite in low-temperature (?800–900?°C), strongly metasomatised mantle xenoliths from the ?84 Ma Bultfontein kimberlite (South Africa). Previous U/Pb dating of the LIMA phases was used to argue that each xenolith recorded a single event of LIMA crystallisation at ?180–190 Ma, coeval with the emplacement of Karoo magmas. SEM imaging reveals that up to four types of LIMA phases coexist in each xenolith, and occasionally in a single LIMA grain. Major element and in situ Sr isotope analyses of the different LIMA types show that each phase has a distinct elemental composition and initial 87Sr/86Sr ratio (e.g., 0.7068–0.7086 and 0.7115–0.7129 for two LIMA types in a single xenolith; 0.7053-0.7131 across the entire sample suite). These combined age and isotopic constraints require that multiple fluids metasomatised these rocks at broadly the same time (i.e. within a few thousands to millions of years), and produced similar mineralogical features. Elemental and isotopic variations between different LIMA types could be due to interaction between one (or more) Karoo-related Ti-rich silicate melts and previously metasomatised, phlogopite-rich lithospheric mantle. This study demonstrates that mantle metasomatic assemblages seemingly generated in a single event may instead result from the infiltration of broadly coeval fluids with variable compositions. This in turn implies that the isotopic variations recorded in mantle rocks may be an inherent feature of metasomatism, and that hot fluids infiltrating a rock do not necessarily cause equilibration at the cm scale, as has been assumed previously. Simple modelling of solid-state diffusion in mantle minerals shows that isotopic disequilibrium may be preserved for up to hundreds of Myr at mantle lithosphere temperatures (?1100–1200?°C), unless subsequently affected by transient heating and/or fluid infiltration events. Radiogenic isotope disequilibrium associated with mantle metasomatism may therefore be a common feature of mantle xenoliths.
Abstract:
Kimberlites are ultrabasic, Si-undersaturated, low Al, low Na rocks rich in CO2 and H2O. The distinctive geochemical character of kimberlite is strongly influenced by the nature of the local underlying lithospheric mantle. Despite this, incompatible trace element ratios and radiogenic isotope characteristics of kimberlites, filtered for the effects of crustal contamination and alteration, closely resemble rocks derived from the deeper, more primitive, convecting mantle. This suggests that the ultimate magma source is sub-lithospheric. Although the composition of primitive kimberlite melt remains unresolved, kimberlites are likely derived from the convecting mantle, with possible source regions ranging from just below the lithosphere, through the transition zone, to the core-mantle boundary.
Abstract: The trace element and radiogenic isotope systematics of clinopyroxene have frequently been used to characterise mantle metasomatic processes, because it is the main host of most lithophile elements in the lithospheric mantle. To further our understanding of mantle metasomatism, both solution-mode Sr-Nd-Hf-Pb and in situ trace element and Sr isotopic data have been acquired for clinopyroxene grains from a suite of peridotite (lherzolites and wehrlites), MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside), and PIC (Phlogopite-Ilmenite-Clinopyroxene) rocks from the Kimberley kimberlites (South Africa). The studied mantle samples can be divided into two groups on the basis of their clinopyroxene trace element compositions, and this subdivision is reinforced by their isotopic ratios. Type 1 clinopyroxene, which comprises PIC, wehrlite, and some sheared lherzolite samples, is characterised by low Sr (~100-200 ppm) and LREE concentrations, moderate HFSE contents (e.g., ~40-75 ppm Zr; La/Zr < 0.04), and restricted isotopic compositions (e.g., 87Sr/86Sri = 0.70369-0.70383; ?Ndi = +3.1 to +3.6) resembling those of their host kimberlite magmas. Available trace element partition coefficients can be used to show that Type 1 clinopyroxenes are close to being in equilibrium with kimberlite melt compositions, supporting a genetic link between kimberlites and these metasomatised lithologies. Thermobarometric estimates for Type 1 samples in this study indicate equilibration depths of 135-160 km within the lithosphere, thus showing that kimberlite melt metasomatism is prevalent in the deeper part of the lithosphere beneath Kimberley. In contrast, Type 2 clinopyroxenes occur in MARID rocks and coarse granular lherzolites in this study, which derive from shallower depths (<135 km), and have higher Sr (~350-1000 ppm) and LREE contents, corresponding to higher La/Zr of > ~ 0.05. The isotopic compositions of Type 2 clinopyroxenes are more variable and extend from compositions resembling the “enriched mantle” towards those of Type 1 rocks (e.g., ?Ndi = ?12.7 to ?4.4). To constrain the source of these variations, in situ Sr isotope analyses of clinopyroxene were undertaken, including zoned grains in Type 2 samples. MARID and lherzolite clinopyroxene cores display generally radiogenic but variable 87Sr/86Sri values (0.70526-0.71177), which are correlated with Sr contents and La/Zr ratios, and which might be explained by the interaction between peridotite and melts from different enriched sources within the lithospheric mantle. Most notably, the rims of these Type 2 clinopyroxenes trend towards compositions similar to those of the host kimberlite and Type 1 clinopyroxene from PIC and wehrlites. These results are interpreted to represent clinopyroxene overgrowth during late-stage (shortly before/during entrainment) metasomatism by kimberlite magmas. Our study shows that a pervasive, alkaline metasomatic event caused MARID to be generated and harzburgites to be converted to lherzolite in the lithospheric mantle beneath the Kimberley area, which was followed by kimberlite metasomatism during Cretaceous magmatism. This latter event is the time at which discrete PIC, wehrlite, and sheared lherzolite lithologies were formed, and MARID and granular lherzolites were partly modified.
Science Advances, doi.10.1126/sciadv.abj1325 1p. Pdf
Mantle
subduction
Abstract: Earth’s carbon cycle is strongly influenced by subduction of sedimentary material into the mantle. The composition of the sedimentary subduction flux has changed considerably over Earth’s history, but the impact of these changes on the mantle carbon cycle is unclear. Here, we show that the carbon isotopes of kimberlite magmas record a fundamental change in their deep-mantle source compositions during the Phanerozoic Eon. The 13C/12C of kimberlites before ~250 Ma preserves typical mantle values, whereas younger kimberlites exhibit lower and more variable ratios-a switch coincident with a recognized surge in kimberlite magmatism. We attribute these changes to increased deep subduction of organic carbon with low 13C/12C following the Cambrian Explosion when organic carbon deposition in marine sediments increased significantly. These observations demonstrate that biogeochemical processes at Earth’s surface have a profound influence on the deep mantle, revealing an integral link between the deep and shallow carbon cycles.
Abstract: Mantle-derived eclogite xenoliths are key for studying the evolution of the cratonic lithosphere, because geochemical evidence suggests that they typically represent fragments of Archean and Proterozoic oceanic lithosphere [1]. Recently, it has been suggested that eclogite xenoliths can serve as redox sensors of the Precambrian upper mantle using V/Sc as a redox proxy [2]. However, metasomatism can change the original oxidation state of the cratonic mantle [3], thereby limiting its use for monitoring mantle redox evolution. Circa 1.8–2.2 Ga eclogite xenoliths erupted with Jurassic kimberlites of the northern Slave craton have geochemical features that indicate oceanic crust protoliths [4, 5]. Such Paleoproterozoic ages are common for Slave craton mantle eclogites [6], linking eclogite formation with 1.9 Ga subduction-collision events at the western craton margin. The eclogites studied here have highly variable Fe3+/?Fe (0.019 – 0.076 ±0.01), with logfO2 (?FMQ-4 to +2 ±0.5) that are both relatively oxidized and reduced compared to Slave mantle peridotite xenoliths [3]. Also, eclogite fO2 positively correlates with some indicies of metasomatism, such as elevated TiO2 in garnet. In addition to considering the time gap between eclogite formation and kimberlite eruption, the highly variable fO2–depth systematics of the eclogites studied here illustrate the drawbacks of using averaged eclogite fO2 to define the redox evolution of the upper mantle. Despite this, the ca. 2 Ga northern Slave craton eclogites have an average depth-corrected logfO2 of ?FMQ-0.5±1.3 (1?) that overlaps with modern MORB, and complies with the upper mantle redox evolution trend predicted using V/Sc ratios of mantlederived melts [2]. However, given the debate around the secuarity of mantle redox [7], further research into the suitability of mantle eclogites as redox sensors is warranted.
Abstract: The Rae craton is an important part of the Canadian Shield and was amalgamated to the Slave craton at ?? 1.9 Ga [1]. Recent geophysical and geochemical data indicate a protracted geodynamic history [1, 2]. Even though the oxidation state of the Earth’s mantle has an important influence of fluid compositions and melting behavior, no data on the oxidation state of the Rae’s mantle are available. The aims of this study were to 1) determine the oxidation state (ƒO2) of the lithosphere beneath the Rae craton, 2) link these results to potential metasomatic overprints and 3) compare the geochemical evolution with the Slave craton. We studied 5 peridotite xenoliths from Pelly Bay (central craton) and 22 peridotites from Somerset Island (craton margin). Pelly Bay peridotites give T < 905°C and depths of ??80- 130 km. Garnets have depleted or “normal” REE patterns, the latter samples recording fO2 values ??0.5 log units higher. The deeper samples are more enriched and oxidised. Peridotites from Somerset Island record T ??825-1190°C, a ?logfO2 ranging from ?? FMQ - FMQ-3.6 from a depth interval of ??100-150 km. Garnets exhibit two REE signatures - sinusoidal and “normal” - indicating an evolutionary sequence of increasing metasomatic re-enrichment and a shift from fluid to melt dominated metasomatism. Compared to the Slave craton, the Rae mantle is more reduced at ??80km but becomes up to 2 log units more oxidised (up to ??FMQ-1) at ??100-130 km. Similar oxidising conditions can be found >140 km in the Slave mantle [3]. Especially under Somerset Island, the lithospheric mantle has contrasting fO2 and metasomatic overprints in the same depth range, which may represent juxtaposed old and rejuvenated domains [2].
Geophysical Research abstracts, EGU, EGU2019-9348, 1p. Pdf
Canada
geodynamics
Abstract: We present the first oxidation state measurements for the subcontinental lithospheric mantle (SCLM) beneath the Rae craton, northern Canada, one of the largest components of the Canadian shield. In combination with major and trace element compositions for garnet and clinopyroxene, we assess the relationship between oxidation state and metasomatic overprinting. The sample suite comprises peridotite xenoliths from the central part (Pelly Bay) and the craton margin (Somerset Island) providing insights into lateral and vertical variations in lithospheric character. Our suite contains spinel, garnet-spinel and garnet peridotites, with most samples originating from 100 to 140 km depth. Within this narrow depth range we observe strong chemical gradients, including variations in oxygen fugacity (ƒO2) of over 4 log units. Both Pelly Bay and Somerset Island peridotites reveal a change in metasomatic type with depth. Observed geochemical systematics and textural evidence support the notion that Rae SCLM developed through amalgamation of different local domains, establishing chemical gradients from the start. These gradients were subsequently modified by migrating melts that drove further development of different types of metasomatic overprinting and variable oxidation at a range of length scales. This oxidation already apparent at ~?100 km depth could have locally destabilised any pre-existing diamond or graphite.
Abstract: We present the first oxidation state measurements for the subcontinental lithospheric mantle (SCLM) beneath the Rae craton, northern Canada, one of the largest components of the Canadian shield. In combination with major and trace element compositions for garnet and clinopyroxene, we assess the relationship between oxidation state and metasomatic overprinting. The sample suite comprises peridotite xenoliths from the central part (Pelly Bay) and the craton margin (Somerset Island) providing insights into lateral and vertical variations in lithospheric character. Our suite contains spinel, garnet-spinel and garnet peridotites, with most samples originating from 100 to 140 km depth. Within this narrow depth range we observe strong chemical gradients, including variations in oxygen fugacity (ƒO2) of over 4 log units. Both Pelly Bay and Somerset Island peridotites reveal a change in metasomatic type with depth. Observed geochemical systematics and textural evidence support the notion that Rae SCLM developed through amalgamation of different local domains, establishing chemical gradients from the start. These gradients were subsequently modified by migrating melts that drove further development of different types of metasomatic overprinting and variable oxidation at a range of length scales. This oxidation already apparent at ~?100 km depth could have locally destabilised any pre-existing diamond or graphite.
Hopp, J., Trieloff, M., Brey, G.P., Woodland, A.B., Simon, N.S.C., Wijbrans, J.R., Siebel, W., Reitter, E.
40 Ar 39 Ar ages of phlogopite in mantle xenoliths from South African kimberlites: evidence for metasomatic mantle impregnation during Kilbaran orogenic cycle.
An oxygen fugacity profile through the Siberian craton - Fe K-edge XANES determinations of Fe3 Fe in garnets in peridotite xenoliths from the Udachnaya East kimberlite.
An experimental study of Fe oxidation states in garnet and clinopyroxene as a function of temperature in the system CaO FeO Fe2O3 MgO Al2O3 SiO2: implications for garnet-clinopyroxene geothermometry.
Contributions to Mineralogy and Petrology, Vol. 164, 4, pp. 623-639.
Contributions to Mineralogy and Petrology, Vol. 170, 25p.
Technology
Experimental petrology
Abstract: Melting of carbonated sediment in the presence of graphite or diamond was experimentally investigated at 7.5–12 GPa and 800–1600 °C in a multianvil apparatus. Two starting materials similar to GLOSS of Plank and Langmuir (Chem Geol 145:325–394, 1998) were prepared from oxides, carbonates, hydroxides and graphite. One mixture (Na-gloss) was identical in major element composition to GLOSS, and the other was poorer in Na and richer in K (K-gloss). Both starting mixtures contained ~6 wt% CO2 and 7 wt% H2O and were doped at a ~100 ppm level with a number of trace elements, including REE, LILE and HFSE. The near-solidus mineral assemblage contained a silica polymorph (coesite or stishovite), garnet, kyanite, clinopyroxene, carbonates (aragonite and magnesite-siderite solid solution), zircon, rutile, bearthite and hydrous phases (phengite and lawsonite at <9 GPa and the hydrous aluminosilicates topaz-OH and phase egg at >10 GPa). Hydrous phases disappear at ~900 °C, and carbonates persist up to 1000-1100 °C. At temperatures >1200 °C, the mineral assemblage consists of coesite or stishovite, kyanite and garnet. Clinopyroxene stability depends strongly on the Na content in the starting mixture; it remains in the Na-gloss composition up to 1600 °C at 12 GPa, but was not observed in K-gloss experiments above 1200 °C. The composition of melt or fluid changes gradually with increasing temperature from hydrous carbonate-rich (<10 wt% SiO2) at 800-1000 °C to volatile-rich silicate liquids (up to 40 wt% SiO2) at high temperatures. Trace elements were analyzed in melts and crystalline phases by LA ICP MS. The garnet-melt and clinopyroxene-melt partition coefficients are in general consistent with results from the literature for volatile-free systems and silicocarbonate melts derived by melting carbonated peridotites. Most trace elements are strongly incompatible in kyanite and silica polymorphs (D < 0.01), except for V, Cr and Ni, which are slightly compatible in kyanite (D > 1). Aragonite and Fe-Mg carbonate have very different REE partition coefficients (D Mst-Sd/L ~ 0.01 and D Arg/L ~ 1). Nb, Ta, Zr and Hf are strongly incompatible in both carbonates. The bearthite/melt partition coefficients are very high for LREE (>10) and decrease to ~1 for HREE. All HFSE are strongly incompatible in bearthite. In contrast, Ta, Nb, Zr and Hf are moderately to strongly compatible in ZrSiO4 and TiO2 phases. Based on the obtained partition coefficients, the composition of a mobile phase derived by sediment melting in deep subduction zones was calculated. This phase is strongly enriched in incompatible elements and displays a pronounced negative Ta-Nb anomaly but no Zr-Hf anomaly. Although all experiments were conducted in the diamond stability field, only graphite was observed in low-temperature experiments. Spontaneous diamond nucleation and the complete transformation of graphite to diamond were observed at temperatures above 1200-1300 °C. We speculate that the observed character of graphite-diamond transformation is controlled by relationships between the kinetics of metastable graphite dissolution and diamond nucleation in a hydrous silicocarbonate melt that is oversaturated in C.
Contributions to Mineralogy and Petrology, Vol. 171, pp. 101-
Technology
Eclogite
Abstract: Clinopyroxene is an essential mineral in eclogitic rocks. It commonly contains minor amounts of the defect-bearing Ca-Eskola (CaEs, Ca0.5?0.5AlSi2O6) component, with higher concentrations generally considered to indicate a high-pressure origin at least within the coesite stability field. Changes in pressure and temperature conditions can lead to exsolution of this component as a free SiO2 phase, which may have a number of petrological implications. This makes it important to understand the factors that maximize CaEs incorporation in clinopyroxene. We have undertaken a series of experiments at high pressures and temperatures (4-10 GPa and 1000-1350 °C) to further investigate the systematics of CaEs incorporation in eclogite-like clinopyroxene and the factors responsible for maximizing CaEs contents. Two simple chemical systems were chosen that allow unambiguous interpretation of the results: (1) CMAS + H2O and (2) two compositions in the NCMAS system. All experimental products contained clinopyroxene and garnet along with either a free SiO2 phase or a silicate melt. Coexisting garnet is grossular-rich, generally with Xgr ? 0.67. Compositional variations are attributable to the presence or absence of melt and changes in modal amounts of garnet at different pressure-temperature conditions. Even small amounts of H2O lower the solidus temperature and the presence of a melt reduces the SiO2 activity, which destabilizes the CaEs component in clinopyroxene. The CaEs and the Ca-Tschermaks (CaTs, CaAl2SiO6) components in clinopyroxene decrease with increasing jadeite mole fraction, which is also a function of pressure and bulk Al content. Modeling X-ray powder diffraction data yields a molar volume for the CaEs endmember of VCaEs = 60.87(63) cm3, which reasonably agrees with a literature value that was estimated from natural samples. In the presence of coexisting coesite, the CaEs and CaTs do not vary independently of each other, being controlled by the internal equilibrium 2CaEs = CaTs + 3SiO2 (coesite). This relation, observed in simple systems (i.e., CMAS ± Na), is also obeyed by clinopyroxene in more complex, natural analog bulk compositions. An assessment of available experimental data reveals a maximum of 15-18 mol% CaEs in eclogitic clinopyroxene at conditions corresponding to 130-180 km depth. CaEs contents are maximized at high temperatures; i.e., at or near the solidus in the presence of coesite. Thus, this study supports the role of CaEs exsolution in contributing to melt generation during upwelling of eclogite bodies in the mantle, albeit with some caveats. Somewhat higher maximum CaEs contents (~20 mol%) are found in Ca and Al-rich bulk compositions, such as grospydite xenoliths. Such bulk compositions also seem to require the coexistence of kyanite. Other Ca and Al-rich rock types, like rodingites, should have the potential of containing CaEs-rich clinopyroxenes, except that they are SiO2-undersaturated. This emphasizes the further role of bulk composition, in addition to high temperatures, in achieving maximum CaEs contents in high-pressure clinopyroxene.
Abstract: Mantle-derived eclogite and pyroxenite xenoliths from the Jurassic Voyageur kimberlite on the northern Slave craton in Arctic Canada were studied for garnet and clinopyroxene major and trace element compositions, clinopyroxene Pb and garnet O isotopic compositions, and garnet Fe3 +/?Fe contents. The Voyageur xenoliths record a wide range of pressures, but are cooler compared to mantle xenoliths derived from the nearby, coeval Jericho kimberlite. The CaO, TiO2 and Zr contents of Voyageur eclogites increase with depth, which is also observed in northern Slave peridotite xenoliths, demonstrating ‘bottom-up’ metasomatic processes within cratonic mantle lithosphere. The Voyageur eclogites have positive Eu anomalies, flat HREEN patterns, and major element compositions that are consistent with ultimate origins from basaltic and gabbroic protoliths within oceanic lithosphere. Clinopyroxene Pb isotope ratios intercept the Stacey-Kramers two-stage terrestrial Pb evolution curve at ca. 2.1 Ga, and form an array towards the host kimberlite, indicating isotopic mixing. The 2.1 Ga eclogite formation age broadly overlaps with known Paleoproterozoic subduction and collision events that occurred along the western margin of the Slave craton. Unlike the eclogites, the Voyageur pyroxenites contain garnet with distinctive fractionated HREEN, sinusoidal REE patterns of calculated bulk rocks, and clinopyroxene with 206Pb/204Pb ratios that intercept the Stacey-Kramers curve at 1.8 Ga. This suggests a distinct origin as Paleoproterozoic high-pressure mantle cumulates. However, the pyroxenite Pb isotope ratios fall within the eclogite array and could also be explained by protoliths formation at ca. 2.1 Ga followed by minor isotopic mixing during mantle metasomatism. Thus, an alternative scenario involves pyroxenite formation within the mantle section of Paleoproterozoic oceanic lithosphere followed by variable metasomatism after incorporation into cratonic mantle lithosphere. This model allows for a linked petrogenesis of the Voyageur eclogites (crust) and pyroxenites (mantle) as part of the same subducting oceanic slab. Oxygen fugacity determinations for one pyroxenite and ten eclogite xenoliths show a range of 3 log units, from ? 4.6 to ? 1.6 ?FMQ, similar to the range observed for nearby Jericho and Muskox eclogites (?FMQ ? 4.2 to ? 1.5). Importantly, the northern Slave eclogite and pyroxenite mantle components are highly heterogeneous in terms of redox state provided that they range from reduced to oxidized relative to Slave peridotite xenoliths. Moreover, the Voyageur eclogites do not exhibit any trend between oxidation state and equilibration depth, which contrasts with the downward decrease in fO2 shown by Slave and worldwide cratonic peridotite xenoliths. Our investigation of mantle eclogite and pyroxenite fO2 reinforces the important influence of recycled mafic components in upper mantle processes, because their high and variable redox buffering capacity strongly controls volatile speciation and melting relations under upper mantle conditions.
Earth and Planetary Science Letters, Vol. 474, pp. 283-295.
Africa, South Africa
deposit - Lace
Abstract: Reconstructing the redox state of the mantle is critical in discussing the evolution of atmospheric composition through time. Kimberlite-borne mantle eclogite xenoliths, commonly interpreted as representing former oceanic crust, may record the chemical and physical state of Archaean and Proterozoic convecting mantle sources that generated their magmatic protoliths. However, their message is generally obscured by a range of primary (igneous differentiation) and secondary processes (seawater alteration, metamorphism, metasomatism). Here, we report the Fe3+/?Fe ratio and ?18 O in garnet from in a suite of well-characterised mantle eclogite and pyroxenite xenoliths hosted in the Lace kimberlite (Kaapvaal craton), which originated as ca. 3 Ga-old ocean floor. Fe3+/?Fe in garnet (0.01 to 0.063, median 0.02; n = 16) shows a negative correlation with jadeite content in clinopyroxene, suggesting increased partitioning of Fe3+ into clinopyroxene in the presence of monovalent cations with which it can form coupled substitutions. Jadeite-corrected Fe3+/?Fe in garnet shows a broad negative trend with Eu*, consistent with incompatible behaviour of Fe3+ during olivine-plagioclase accumulation in the protoliths. This trend is partially obscured by increasing Fe3+ partitioning into garnet along a conductive cratonic geotherm. In contrast, NMORB-normalised Nd/Yb - a proxy of partial melt loss from subducting oceanic crust (<1) and metasomatism by LREE-enriched liquids (>1) - shows no obvious correlation with Fe3+/?Fe, nor does garnet ?18OVSMOW (5.14 to 6.21‰) point to significant seawater alteration. Median bulk-rock Fe3+/?Fe is roughly estimated at 0.025. This observation agrees with V/Sc systematics, which collectively point to a reduced Archaean convecting mantle source to the igneous protoliths of these eclogites compared to the modern MORB source. Oxygen fugacites (fO2) relative to the fayalite-magnetite-quartz buffer (FMQ) range from ?log ? fO2 = FMQ-1.3 to FMQ-4.6. At those reducing conditions, the solubility of carbon in the fluids released by dehydration is higher than in fluids closer to FMQ. The implication is that Archean processes of C transport and deposition would have differed from those known in modern-style subduction zones, and diamond would have formed from methane-rich fluids. In addition, such reducing material could drive redox melting or freezing upon deep recycling and migration of CH4-bearing fluids into the ambient mantle.
Abstract: Diamond nucleation and growth were investigated experimentally at 7.5 and 10.5?GPa and temperatures up to 1500?°C. Samples consisted of two layers: i) H2O- and CO2-bearing model sediment and ii) graphite-bearing garnet harzburgite comprising natural minerals. Two experimental series were conducted, one under a controlled temperature gradient with the sedimentary layer usually in the cold zone and the other under isothermal conditions. In the latter case, diamond seeds were added to the sedimentary mixture. During the experiments, the sedimentary layer partially or completely melted, with the melt percolating and interacting with the adjacent harzburgite. The graphite-to-diamond transition in the peridotite was observed above 1300?°C at 7.5?GPa and 1200?°C at 10.5?GPa in the temperature-gradient experiments, and at temperatures ~100?°C lower in the isothermal experiments with diamond seeds. Newly formed diamond occurs mostly as individual grains up to 10??m in size and is separate from graphite aggregates. In some cases, an association of diamond with magnesite was observed. Diamond nucleation occurs in hydrous and CO2-bearing silicate melt following graphite dissolution and recrystallization. In the case of the diamond-magnesite association, diamond was probably formed through carbonate reduction coupled with graphite oxidation. The composition of the melts ranged from “carbonatitic” with ~10?wt% SiO2 and?>?50?wt% volatiles to hydrous silicate with ~40?wt% SiO2 and?
Abstract: Subduction zone magmas are more oxidised on eruption than those at mid-ocean ridges. This is attributed either to oxidising components, derived from subducted lithosphere (slab) and added to the mantle wedge, or to oxidation processes occurring during magma ascent via differentiation. Here we provide direct evidence for contributions of oxidising slab agents to melts trapped in the sub-arc mantle. Measurements of sulfur (S) valence state in sub-arc mantle peridotites identify sulfate, both as crystalline anhydrite (CaSO4) and dissolved SO42? in spinel-hosted glass (formerly melt) inclusions. Copper-rich sulfide precipitates in the inclusions and increased Fe3+/?Fe in spinel record a S6+Fe2+ redox coupling during melt percolation through the sub-arc mantle. Sulfate-rich glass inclusions exhibit high U/Th, Pb/Ce, Sr/Nd and ?34S (+?7 to +?11‰), indicating the involvement of dehydration products of serpentinised slab rocks in their parental melt sources. These observations provide a link between liberated slab components and oxidised arc magmas.
Nature Research Scientific Reports, https://doi.org/10.1038/ s41598-019-55743-1 11p. Pdf
Mantle
melting, redox
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Oxygen fugacity (fO2) is an intensive variable implicated in a range of processes that have shaped the Earth system, but there is controversy on the timing and rate of oxidation of the uppermost convecting mantle to its present fO2 around the fayalite-magnetite-quartz oxygen buffer. Here, we report Fe3+/?Fe and ƒf2 for ancient eclogite xenoliths with oceanic crustal protoliths that sampled the coeval ambient convecting mantle. Using new and published data, we demonstrate that in these eclogites, two redox proxies, V/Sc and Fe3+/?Fe, behave sympathetically, despite different responses of their protoliths to differentiation and post-formation degassing, seawater alteration, devolatilisation and partial melting, testifying to an unexpected robustness of Fe3+/?Fe. Therefore, these processes, while causing significant scatter, did not completely obliterate the underlying convecting mantle signal. Considering only unmetasomatised samples with non-cumulate and little-differentiated protoliths, V/Sc and Fe3+/?Fe in two Archaean eclogite suites are significantly lower than those of modern mid-ocean ridge basalts (MORB), while a third suite has ratios similar to modern MORB, indicating redox heterogeneity. Another major finding is the predominantly low though variable estimated fO2 of eclogite at mantle depths, which does not permit stabilisation of CO2-dominated fluids or pure carbonatite melts. Conversely, low-fO2 eclogite may have caused efficient reduction of CO2 in fluids and melts generated in other portions of ancient subducting slabs, consistent with eclogitic diamond formation ages, the disproportionate frequency of eclogitic diamonds relative to the subordinate abundance of eclogite in the mantle lithosphere and the general absence of carbonate in mantle eclogite. This indicates carbon recycling at least to depths of diamond stability and may have represented a significant pathway for carbon ingassing through time.
Abstract: Eclogite mantle xenoliths from various kimberlite occurrences on the Kaapvaal craton show evidence for depth- and redox-dependent metasomatic events that led to variable base metal sulphide and incompatible element enrichments. Eclogite xenoliths from the Roberts Victor, Jagersfontein, Kimberley (Kamfersdam) and Premier kimberlites were investigated for their silicate and base metal sulphide geochemistry, stable oxygen isotope compositions and oxybarometry. The variably metasomatised eclogites had basaltic, picritic and gabbroic protolith compositions and have garnet ?18O values that range from +3.3 to +7.9‰, which, when coupled with the trace element characteristics, indicate oceanic lithosphere protoliths that had undergone variable degrees of seawater alteration. The deepest equilibrated eclogites (175220?km depth) from near the base of the Kaapvaal craton lithosphere are the most refractory and feature significant light rare earth element (LREE) depletions. They show the most oxidised redox compositions with ?logƒO2 values of FMQ-3.9 to FMQ-1.5. Subtle metasomatic overprinting of these eclogites resulted in base metal sulphide formation with relatively depleted and highly fractionated HSE compositions. These deepest eclogites and their included base metal sulphides suggest interaction with relatively oxidised melts or fluids, which, based on their HSE characteristics, could be related to precursor kimberlite metasomatism that was widespread within the Kaapvaal craton mantle lithosphere. In contrast, eclogites that reside at shallower, “mid-lithospheric” depths (140180?km) have been enriched in LREE and secondary diopside/phlogopite. Importantly, they host abundant metasomatic base metal sulphides, which have higher HSE contents than those in the deeper eclogites at the lithosphere base. The mid-lithospheric eclogites have more reducing redox compositions (?logfO2?=?FMQ-5.3 ? FMQ-3.3) than the eclogites from the lowermost Kaapvaal lithosphere. The compositional overprint of the shallower mantle eclogites resembles basaltic rather than kimberlitic/carbonatitic metasomatism, which is also supported by their relatively reducing redox state. Base metal sulphides from the mid-lithospheric eclogites have HSE abundances and distributions that are similar to Karoo flood basalts from southern Africa, suggesting a link between the identified shallow mantle metasomatism of the Kaapvaal cratonic lithosphere and the Karoo large igneous event during the Mesozoic. The sulphide-hosted platinum group element abundances of the mid-lithospheric eclogites are higher compared with their analogues from the deeper lithospheric eclogites, which in combination with their contrasting oxidation states, may imply redox-controlled HSE mobility during sulphur-rich metasomatism of continental mantle lithosphere.
deposit - Roberts Victor, Jagersfontein, Kimberley, Kamfersdam, Premier
Abstract: Eclogite mantle xenoliths from various kimberlite occurrences on the Kaapvaal craton show evidence for depth- and redox-dependent metasomatic events that led to variable base metal sulphide and incompatible element enrichments. Eclogite xenoliths from the Roberts Victor, Jagersfontein, Kimberley (Kamfersdam) and Premier kimberlites were investigated for their silicate and base metal sulphide geochemistry, stable oxygen isotope compositions and oxybarometry. The variably metasomatised eclogites had basaltic, picritic and gabbroic protolith compositions and have garnet ?18O values that range from +3.3 to +7.9‰, which, when coupled with the trace element characteristics, indicate oceanic lithosphere protoliths that had undergone variable degrees of seawater alteration. The deepest equilibrated eclogites (175-220 km depth) from near the base of the Kaapvaal craton lithosphere are the most refractory and feature significant light rare earth element (LREE) depletions. They show the most oxidised redox compositions with ?logƒO2 values of FMQ-3.9 to FMQ-1.5. Subtle metasomatic overprinting of these eclogites resulted in base metal sulphide formation with relatively depleted and highly fractionated HSE compositions. These deepest eclogites and their included base metal sulphides suggest interaction with relatively oxidised melts or fluids, which, based on their HSE characteristics, could be related to precursor kimberlite metasomatism that was widespread within the Kaapvaal craton mantle lithosphere. In contrast, eclogites that reside at shallower, “mid-lithospheric” depths (140-180 km) have been enriched in LREE and secondary diopside/phlogopite. Importantly, they host abundant metasomatic base metal sulphides, which have higher HSE contents than those in the deeper eclogites at the lithosphere base. The mid-lithospheric eclogites have more reducing redox compositions (?logfO2 = FMQ-5.3 ? FMQ-3.3) than the eclogites from the lowermost Kaapvaal lithosphere. The compositional overprint of the shallower mantle eclogites resembles basaltic rather than kimberlitic/carbonatitic metasomatism, which is also supported by their relatively reducing redox state. Base metal sulphides from the mid-lithospheric eclogites have HSE abundances and distributions that are similar to Karoo flood basalts from southern Africa, suggesting a link between the identified shallow mantle metasomatism of the Kaapvaal cratonic lithosphere and the Karoo large igneous event during the Mesozoic. The sulphide-hosted platinum group element abundances of the mid-lithospheric eclogites are higher compared with their analogues from the deeper lithospheric eclogites, which in combination with their contrasting oxidation states, may imply redox-controlled HSE mobility during sulphur-rich metasomatism of continental mantle lithosphere.
Earth and Planetary Science Letters, doi.org/10.1016/ j.epsl.2020. 116720 19p. Pdf
Africa, South Africa
deposit - Bellsbank
Abstract: The nature of the deep calcium geochemical cycle through time is unresolved, in part due to the dearth of information about the calcium isotope composition of Archean recycled oceanic crust. Remnants of such ancient oceanic crust are preserved in the form of cratonic mantle eclogites, brought to surface as xenoliths in kimberlite magma eruptions. The ? 44 / 40Ca of fresh mantle-derived eclogite xenoliths (i.e., garnet and omphacite mineral separates) from the Bellsbank kimberlite on the Kaapvaal craton in South Africa are presented here in combination with their trace element compositions, garnet Fe3+ contents and ?18O values. The studied Bellsbank eclogite xenoliths have geochemical compositions that indicate oceanic crustal protoliths, with bulk Al2O3 from 15 to 27 wt.%, Eu anomalies from 0.8 to 2.6 and, significantly, garnet ?18O values from +2.7 to +6.2‰. Garnet Fe3+/?Fe contents yield logfO2(?FMQ) values between -4.0 and -1.2 for a depth range of 110-180 km, recording strong redox heterogeneity of the eclogite component within the Archean Kaapvaal mantle lithosphere. Reconstructed bulk eclogite MgO contents correlate negatively with fO2, suggesting that the redox compositions are related to magmatic differentiation during oceanic crust formation, excluding secondary metasomatic overprints. These data may thus emphasize that Archean basaltic oceanic crust had a similarly variable redox composition to modern MORB-type crust. Reconstructed bulk ? 44 / 40Ca values for the Bellsbank eclogites range from +0.28 to +1.56‰. Although some of the xenoliths have ? 44 / 40Ca values that overlap with the average mantle composition and modern MORB (+0.94 ± 0.1 and +0.83 ± 0.05‰), half of our dataset shows excursions to more extreme Ca isotopic compositions. Both higher and lower ? 44 / 40Ca relative to mantle compositions are recorded by the eclogites, with a general negative correlation with ?18O suggestive of seawater-alteration of oceanic crust. The combined low ? 44 / 40Ca (+0.28‰) and ?18O (+3.4‰) measured for one eclogite xenolith may record a subtle imprint by carbonate-rich mantle melts, which are known to contain isotopically light calcium contributed by recycled sediments. In contrast, the high ? 44 / 40Ca of up to +1.56‰ for some eclogite xenoliths, coupled with strong LREE depletion, can be explained by calcium isotope fractionation during partial melting. The protracted history of recycled oceanic crust as probed by cratonic mantle eclogites is recorded by their highly variable ? 44 / 40Ca-?18O-fO2 signatures. Whereas some of this heterogeneity can be linked to processes that operated on the Archean ocean floor such as seawater-alteration of basaltic crust, other sources of compositional variability are introduced by loss and addition of melts during subduction recycling and mantle residence. The observed ? 44 / 40Ca complexity of ancient recycled oceanic crust components at the scale of a single mantle-derived eclogite xenolith suite implies that mantle plume sourced intraplate magmas should reveal similarly strong calcium isotope variations contributed by apparently essential recycled crust components - as observed in the global oceanic island basalt record.
Nature Scientific Reports, 10.1038/s41598-021-83261-6 11p. Pdf
Canada, Northwest Territories
metasomatism
Abstract: We present the first oxidation state measurements for the subcontinental lithospheric mantle (SCLM) beneath the Rae craton, northern Canada, one of the largest components of the Canadian shield. In combination with major and trace element compositions for garnet and clinopyroxene, we assess the relationship between oxidation state and metasomatic overprinting. The sample suite comprises peridotite xenoliths from the central part (Pelly Bay) and the craton margin (Somerset Island) providing insights into lateral and vertical variations in lithospheric character. Our suite contains spinel, garnet-spinel and garnet peridotites, with most samples originating from 100 to 140 km depth. Within this narrow depth range we observe strong chemical gradients, including variations in oxygen fugacity (ƒO2) of over 4 log units. Both Pelly Bay and Somerset Island peridotites reveal a change in metasomatic type with depth. Observed geochemical systematics and textural evidence support the notion that Rae SCLM developed through amalgamation of different local domains, establishing chemical gradients from the start. These gradients were subsequently modified by migrating melts that drove further development of different types of metasomatic overprinting and variable oxidation at a range of length scales. This oxidation already apparent at ~?100 km depth could have locally destabilised any pre-existing diamond or graphite.
Abstract: The central region of the Kaapvaal craton is relatively understudied in terms of its lithospheric mantle architecture, but is commonly believed to be significantly impacted by post-Archean magmatism such as the ca. 2056 Ma Bushveld large igneous event. We investigate a collection of 17 eclogite xenoliths from the Cretaceous Palmietfontein kimberlite at the Western Limb of the Bushveld Complex for their mineralogical compositions (major and trace elements, plus Fe3+ contents), as well as stable oxygen and radiogenic Pb isotopic compositions to gain further insights into the nature and evolution of the central Kaapvaal cratonic mantle lithosphere. New U/Pb age determinations on mantle-derived zircon yield a magma emplacement age of ca. 75 Ma for the Palmietfontein Group-1 kimberlite, which means that the entrained eclogite xenoliths may record a protracted metasomatic history from the Proterozoic through to most of the Phanerozoic eon. Garnet ?18O values of up to 6.9‰ and positive Eu anomalies for the bulk rocks suggest seawater-altered oceanic crustal protoliths for the Palmietfontein eclogite xenolith suite, which is typical for the eclogitic components of the Kaapvaal root and other cratonic mantle sections worldwide. However, several features of the Palmietfontein eclogites are commonly not observed in other mantle-derived eclogite xenolith suites. Firstly, the samples studied yield relatively low equilibration pressures and temperatures between 2.7 and 4.5 GPa and 740-1064 °C, indicating a relatively shallow residence between 90 and 150 km depths. Secondly, euhedral coarse amphibole is present in several eclogite nodules where it is in equilibrium with ‘touching’ garnet, supporting eclogite residence within the amphibole stability field at uppermost lithospheric mantle conditions. Thirdly, primary omphacitic clinopyroxene is often overgrown by diopside, and is significantly enriched in incompatible trace elements. The clinopyroxene is also characterized by elevated 206Pb/204Pb of 17.28-19.20 and 207Pb/204 Pb of 15.51-16.27, and these Pb isotopic compositions overlap with those of Mesozoic Group-2 kimberlites from the Kaapvaal craton. Our results show that eclogites reside at ~85 km depth beneath the central Kaapvaal craton as part of a layer that corresponds to an approximately 50 km thick seismically-detected mid-lithospheric discontinuity. Mid-lithospheric discontinuities have been interpreted as metasomatic fronts formed by focussed crystallization of hydrous mineral phases from enriched volatile-bearing melts, and as such the strongly overprinted amphibole-bearing eclogite xenoliths from Palmietfontein may represent a physical expression of such seismically anomalous metasomatic layer at mid-lithospheric depth. Our Pb isotope data suggest that the focussed metasomatism can be attributed to volatile-rich melts reminiscent of potassic Group-2 kimberlites, which have been invoked in MARID-style metasomatic overprinting of the lower lithospheric mantle beneath the western Kaapvaal craton. However, the relatively low fO2 recorded by the Palmietfontein eclogites (minimum FMQ-4.5) suggests that the metasomatism at mid-lithospheric depth was less protracted compared to the more intensive and oxidizing metasomatism typically observed near the base of cratonic mantle roots. While it is possible that Proterozoic magmatic events were responsible for the focussed mid-lithospheric metasomatism of the Kaapvaal mantle, on the basis of the Pb isotope constraints the Palmietfontein eclogites were most likely overprinted during ca. 120 Ma Group-2 kimberlite magmatism.
Tappe, S., Massuyeau, M. , Smart, K.A., Woodland, A.B., Gussone, N., Milne, S., Stracke, A.
Sheared peridotite and megacryst formation beneath the Kaapvaal Craton: a snapshot of tectonomagmetic processes across the lithosphere-asthenosphere transition.
Abstract: The cratonic lithosphere-asthenosphere boundary is commonly invoked as the site of sheared peridotite and megacryst formation, a well-recognized petrological assemblage whose genetic relationships—if any—remain poorly understood. We have undertaken a comprehensive petrology and Sr-Nd-Hf-Ca isotope study of sheared peridotite xenoliths and clinopyroxene megacrysts from the c. 1150 Ma Premier kimberlite pipe on the central Kaapvaal craton in South Africa. New textural and mineral trace element evidence suggests that strong tectonic and magmatic overprinting affected the lower cratonic mantle over a vertical distance of ?50 km from the lithosphere-asthenosphere boundary located at ?200-225 km depth. Although modification of the central Kaapvaal cratonic mantle is commonly linked to the c. 2056 Ma Bushveld large igneous event, our thermobarometry, mantle redox, and Sr-Nd-Hf-Ca isotope data support a model in which volatile-rich low-volume melts and associated high-density fluids refertilized the lithosphere base shortly before or during asthenosphere-derived kimberlite and carbonatite magmatism at around 1150 Ma. This episode of lithospheric mantle enrichment was facilitated by exceptionally strong shear movements, as are recorded in the plastically deformed peridotites. We argue that stress-driven segregation of percolating carbonated melts contributed to megacryst formation along, or in close proximity to, shear zones within the cratonic mantle lithosphere. Integration of our results from the Kaapvaal craton and modern petrological concepts allows for the identification of a lithosphere-asthenosphere transition zone between ?150 and 225 km depth. This horizon is defined by intersections of the ?40-42 mW m-2 Premier paleogeotherm with (1) CO2-H2O-present solidus curves for peridotite (upper bound), and (2) typical mantle adiabats with potential temperatures between 1315 and 1420 °C (lower bound). At Premier, the most strongly deformed sheared peridotites occur mainly between ?160 and 185 km depth, firmly within the lithosphere-asthenosphere transition zone. Contrary to many previous models, we suggest that sheared peridotite formation occurs in localized deformation zones spaced out across the entire width of the lithosphere-asthenosphere transition zone, rather than being restricted to a single thin layer at the craton base where mantle flow causes viscous drag. Hence, plate-tectonic stresses acting on the lower cratonic lithosphere may be accommodated by extensive networks of shear zones, which provide transient pathways and sinks for percolating volatile-rich melts, linking the formation of megacrysts and sheared peridotites.
Canada, Ontario, Attawapiskat, Africa, South Africa
deposit - Victor, Finsch, Newlands
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. “Planed” and “ribbed” trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Abstract: Quantitative trace element data from high-purity gem diamonds from the Victor Mine, Ontario, Canada as well as near-gem diamonds from peridotite and eclogite xenoliths from the Finsch and Newlands mines, South Africa, acquired using an off-line laser ablation method show that we see the same spectrum of fluids in both high-purity gem and near-gem diamonds that was previously documented in fibrous diamonds. "Planed" and "ribbed" trace element patterns characterize not only the high-density fluid (HDF) inclusions in fibrous diamonds but also in gem diamonds. Two diamonds from two Finsch harzburgite xenoliths show trace element patterns similar to those of saline fluids, documenting the involvement of saline fluids in the precipitation of gem diamonds, further strengthening the link between the parental fluids of both gem and fibrous diamonds. Differences in trace element characteristics are evident between Victor diamonds containing silicate inclusions compared with Victor diamonds containing sulphide inclusions. The sulphide-bearing diamonds show lower levels of inter-element fractionation and more widely varying siderophile element concentrations - indicating that the silicate and sulphide-bearing diamonds likely formed by gradations of the same processes, via melt-rock reaction or from a subtly different fluid source. The shallow negative LREEN-HREEN slopes displayed by the Victor diamonds establish a signature indicative of original derivation of the diamond forming agent during major melting (~10% melt). Consequently, this signature must have been passed on to HDFs separating from such silicate melts.
Abstract: The physical characteristics and impermeability of diamonds allow them to retain radiogenic 4He produced in-situ from radioactive decay of U, Th and Sm. This study investigates the U-Th/He systematics of fibrous diamonds and provides a first step in quantification of the uncertainties associated with determining the in-situ produced radiogenic 4He concentration. Factors determining the total amount of measured helium in a diamond are the initial trapped 4He, the in-situ produced radiogenic 4He, ?-implantation, ?-ejection, diffusion, and cosmogenic 3He production. Alpha implantation is negligible, and diffusion is slow, but the cosmogenic 3He component can be significant for alluvial diamonds as the recovery depth is unknown. Therefore, samples were grouped based on similar major and trace element compositions to determine possible genetically related samples. A correlation between the 4He and U-Th concentrations approximates the initial 4He concentration at the axis-intersect and age as the slope. In this study, the corrections were applied to eight fibrous cubic diamonds from the Democratic Republic of the Congo and two diamonds from the Jwaneng kimberlite in Botswana. A correlation exists between the 4He and U-Th concentrations of the group ZRC2, 3, and 6, and of the group CNG2, 3, and 4 and both correlations deviate significantly from a 71?Ma kimberlite eruption isochron. The U-Th/He dating method appears a promising new approach to date metasomatic fluid events that result in fibrous diamond formation and this is the first evidence that some fibrous diamonds can be formed 10s to 100s Myr before the kimberlite eruption.
Abstract: Isotope compositions of basalts provide information about the chemical reservoirs in Earth’s interior and play a critical role in defining models of Earth’s structure. However, the helium isotope signature of the mantle below depths of a few hundred kilometers has been difficult to measure directly. This information is a vital baseline for understanding helium isotopes in erupted basalts. We measured He-Sr-Pb isotope ratios in superdeep diamond fluid inclusions from the transition zone (depth of 410 to 660 kilometers) unaffected by degassing and shallow crustal contamination. We found extreme He-C-Pb-Sr isotope variability, with high 3He/4He ratios related to higher helium concentrations. This indicates that a less degassed, high-3He/4He deep mantle source infiltrates the transition zone, where it interacts with recycled material, creating the diverse compositions recorded in ocean island basalts.
Abstract: Marange diamonds (Zimbabwe) contain both fluid-poor (gem-quality) and fluid-bearing growth zones with abundant CH4. As such, they provide the unique opportunity to compare trace element compositions of CH4-bearing diamonds with those of carbonatitic and saline high density fluid (HDF)-bearing diamonds (gem-quality and fibrous) to obtain an overview of mantle source fluids for diamond growth. HDF’s in fibrous diamonds and some gem-quality diamonds have been linked to subduction of surficial material, consistent with the global link between diamond age and collisional tectonic events. Even though Marange diamonds have +?15N indicative of surficial recycling, they do not display the expected Eu or Sr anomalies. Fibrous diamonds have the most fractionated REE patterns, with negligible HREE and high (La/Yb)N ? 100- 10000. Gem-quality diamonds have highly variable (La/Yb)N; the most unfractionated HDF’s are in Victor and Cullinan diamonds with low (La/Yb)N <76. HDF’s in Marange diamonds are intermediate between these two extremes, with (La/Yb)N = 23-240. Differences in (La/Yb)N between different diamond suites relate either to varying initial compositions (where low (La/Yb)N reflects derivation during higher degrees of melting) or to the increasing interaction of HDF’s in fibrous diamonds with mantle rocks during fluid infiltration. Marange diamonds have rare +Ce anomalies, that have so far only been reported for Victor and Brazil (sub-lithospheric) gem-quality diamonds. The oxidation state of Ce (Ce4+ vs Ce3+) and development of Ce anomalies could be attributed to ƒO2, melt/fluid composition, and PT conditions. In Marange, Victor and Brazil diamonds, Ce4+ substitution for Zr4+ does not appear to be a factor since we find no correlation between Zr content and Ce anomalies. However, in Marange diamonds, CH4-bearing zones have less variable Ce anomalies compared to the CH4-free zones, which may suggest Ce anomalies are indicative of fluid oxidation state.
Earth and Planetary Science Letters, Vol. 507, pp. 175-186.
Mantle
peridotite
Abstract: To examine how the mantle lithosphere stabilises continents, we present a synthesis of the mantle beneath Zealandia in the SW Pacific Ocean. Zealandia, Earth's “8th continent”, occurs over 4.9 M km2 and comprises a fore-arc, arc and back-arc fragment rifted from the Australia-Antarctica Gondwana margin 85 Myr ago. The oldest extant crust is ?500 Ma and the majority is Permian-Jurassic. Peridotitic rocks from most known locations reveal the underpinning mantle to comprise regional domains varying from refractory (Al2O3 < 1 wt%, olivine Mg# > 92, spinel Cr# up to 80, Pt/Ir < 1) to moderately depleted (Al2O3 = 2-4 wt%, olivine Mg# ?90.5, spinel Cr# < ?60). There is no systematic distribution of these domains relative to the former arc configuration and some refractory domains underlie crust that is largely devoid of magmatic rocks. Re-depletion Os model ages have no correlation with depletion indices but do have a distribution that is very similar to global convecting mantle. Whole rock, mineral and isotopic data are interpreted to show that the Zealandia mantle lithosphere was constructed from isotopically heterogeneous convecting mantle fragments swept into the sub-arc environment, amalgamated, and variably re-melted under low-P hydrous conditions. The paucity of mafic melt volumes in most of the overlying crust that could relate to the depleted domains requires melting to have been followed by lateral accretion either during subduction or slab rollback. Recent Australia-Pacific convergence has thickened portions of the Zealandia mantle to >160 km. Zealandia shows that the generation of refractory and/or thick continental lithosphere is not restricted to the Archean. Since Archean cratons also commonly display crust-mantle age decoupling, contain spinel peridotites with extreme Cr# numbers that require low-P hydrous melting, and often have a paucity of mafic melts relative to the extreme depletion indicated by their peridotitic roots, they too may - in part - be compilations of peridotite shallowly melted and then laterally accreted at subduction margins.
Abstract: The Mesoproterozoic Midcontinent Rift System (MRS) of North America hosts a diverse suite of magmatic and hydrothermal mineral deposits in the Lake Superior region where rift rocks are exposed at or near the surface. Historically, hydrothermal deposits, such as Michigan’s native copper deposits and the White Pine sediment-hosted stratiform copper deposit, were major MRS metal producers. On-going exploration for and potential development of copper-nickel sulfide deposits hosted by the Duluth Complex of Minnesota and the opening of the Eagle nickel mine in Michigan indicate an expanding interest in MRS magmatic deposits. MRS hydrothermal and magmatic mineral deposits, many of which are significant past, present, and likely future providers of critical minerals, here are placed into a space and time metallogenic framework. To construct this framework, regional MRS mineral deposits extracted from the U.S. Geological Survey Mineral Resources Data System (MRDS) and the Ontario Ministry of Energy, Northern Development and Mines Mineral Deposit Inventory (MDI) were supplemented by other known and recently recognized mineral deposits described in the literature. All mineral deposits were classified by deposit type, host rock age and type, and estimated timing of mineralization. Deposits were then put into a tectonic evolutionary framework (stages) for the MRS, which shows that deposits formed within discrete spatial and temporal stages of rift evolution. Each stage of rift evolution is characterized by specific mineral deposit types that are largely confined both by their physical location in rift rocks and type and timing of mineralization. Examples include MRS nickel-rich conduit-type magmatic sulfide deposits, which are restricted to an early magmatic stage MRS history when magma compositions were characterized by Ni-rich picrites and high Mg basalts. In contrast, contact-type magmatic sulfide deposits with Cu > Ni were derived from more evolved Al-rich tholeiitic magmas that dominated a later time of voluminous magmatic activity. Hydrothermal sediment-hosted stratiform chalcocite mineralization along the margins of western Lake Superior in Michigan is economic only where fluid flow through red beds was concentrated by structures along the margins of a post-volcanic MRS sedimentary basin. Widespread native Cu and native Ag mineralization occurred about 40 million years after formation of host basalt lava flows and interflow sedimentary rocks. These descriptions of the diverse mineral deposits in the Lake Superior region cataloged within the space of the local and regional geology and over the more than 60-million-year mineralizing history of the MRS are indicative of the complex and at times overlapping magmatic and hydrothermal mineral systems that operated within this major large igneous province.
Geological Society of London Special Publication: Continent formation through time., No. 389, pp. 41-67.
Canada, Ontario, Quebec
Geotectonics
Abstract: Hudson Bay Lithospheric Experiment (HuBLE) was designed to understand the processes that formed Laurentia and the Hudson Bay basin within it. Receiver function analysis shows that Archaean terranes display structurally simple, uniform thickness, felsic crust. Beneath the Palaeoproterozoic Trans-Hudson Orogen (THO), thicker, more complex crust is interpreted as evidence for a secular evolution in crustal formation from non-plate-tectonic in the Palaeoarchaean to fully developed plate tectonics by the Palaeoproterozoic. Corroborating this hypothesis, anisotropy studies reveal 1.8 Ga plate-scale THO-age fabrics. Seismic tomography shows that the Proterozoic mantle has lower wavespeeds than surrounding Archaean blocks; the Laurentian keel thus formed partly in post-Archaean times. A mantle transition zone study indicates ‘normal’ temperatures beneath the Laurentian keel, so any cold mantle down-welling associated with the regional free-air gravity anomaly is probably confined to the upper mantle. Focal mechanisms from earthquakes indicate that present-day crustal stresses are influenced by glacial rebound and pre-existing faults. Ambient-noise tomography reveals a low-velocity anomaly, coincident with a previously inferred zone of crustal stretching, eliminating eclogitization of lower crustal rocks as a basin formation mechanism. Hudson Bay is an ephemeral feature, caused principally by incomplete glacial rebound. Plate stretching is the primary mechanism responsible for the formation of the basin itself.
Earth and Planetary Science Letters, Vol. 465, pp. 155-167.
Mantle
Subduction
Abstract: Subduction is integral to mantle convection and plate tectonics, yet the role of the subslab mantle in this process is poorly understood. Some propose that decoupling from the slab permits widespread trench parallel flow in the subslab mantle, although the geodynamical feasibility of this has been questioned. Here, we use the source-side shear wave splitting technique to probe anisotropy beneath subducting slabs, enabling us to test petrofabric models and constrain the geometry of mantle fow. Our global dataset contains 6369 high quality measurements - spanning ?40,000?km?40,000?km of subduction zone trenches - over the complete range of available source depths (4 to 687?km) - and a large range of angles in the slab reference frame. We find that anisotropy in the subslab mantle is well characterised by tilted transverse isotropy with a slow-symmetry-axis pointing normal to the plane of the slab. This appears incompatible with purely trench-parallel flow models. On the other hand it is compatible with the idea that the asthenosphere is tilted and entrained during subduction. Trench parallel measurements are most commonly associated with shallow events (source depth <50?km<50?km) - suggesting a separate region of anisotropy in the lithospheric slab. This may correspond to the shape preferred orientation of cracks, fractures, and faults opened by slab bending. Meanwhile the deepest events probe the upper lower mantle where splitting is found to be consistent with deformed bridgmanite.
Journal of African Earth Sciences, Vol. 134, pp. 10-23.
Africa, Malawi
carbonatite - Songwe Hill
Abstract: Songwe Hill, Malawi, is one of the least studied carbonatites but has now become particularly important as it hosts a relatively large rare earth deposit. The results of new mapping, petrography, geochemistry and geochronology indicate that the 0.8 km diameter Songwe Hill is distinct from the other Chilwa Alkaline Province carbonatites in that it intruded the side of the much larger (4 x 6 km) and slightly older (134.6 ± 4.4 Ma) Mauze nepheline syenite and then evolved through three different carbonatite compositions (C1–C3). Early C1 carbonatite is scarce and is composed of medium–coarse-grained calcite carbonatite containing zircons with a U–Pb age of 132.9 ± 6.7 Ma. It is similar to magmatic carbonatite in other carbonatite complexes at Chilwa Island and Tundulu in the Chilwa Alkaline Province and others worldwide. The fine-grained calcite carbonatite (C2) is the most abundant stage at Songwe Hill, followed by a more REE- and Sr-rich ferroan calcite carbonatite (C3). Both stages C2 and C3 display evidence of extensive (carbo)-hydrothermal overprinting that has produced apatite enriched in HREE (<2000 ppm Y) and, in C3, synchysite-(Ce). The final stages comprise HREE-rich apatite fluorite veins and Mn-Fe-rich veins. Widespread brecciation and incorporation of fenite into carbonatite, brittle fracturing, rounded clasts and a fenite carapace at the top of the hill indicate a shallow level of emplacement into the crust. This shallow intrusion level acted as a reservoir for multiple stages of carbonatite-derived fluid and HREE-enriched apatite mineralisation as well as LREE-enriched synchysite-(Ce). The close proximity and similar age of the large Mauze nepheline syenite suggests it may have acted as a heat source driving a hydrothermal system that has differentiated Songwe Hill from other Chilwa carbonatites.
Alkaline rocks and carbonatites of the World, Part 4: Antarctica, Asia and Europe ( excluding the former USSR), Australasia and Oceanic Islands.
geolsoc.org.uk, Book MPAR4 approx 150.00
Antarctica, Asia, Europe
carbonatites
Abstract: The alkaline igneous rocks and carbonatites are compositionally and mineralogically the most diverse of all igneous rocks and, apart from their scientific interest, are of major, and growing, economic importance. They are important repositories of certain metals and commodities, indeed the only significant sources of some of them, and include Nb, the rare earths, Cu, V, diamond, phosphate, vermiculite, bauxite, raw materials for the manufacture of ceramics, and potentially Th and U. The economic potential of these rocks is now widely appreciated, particularly since the commencement of the mining of the Palabora carbonatite for copper and a host of valuable by-products. Similarly, the crucial economic dominance of rare earth production from carbonatite-related occurrences in China, has stimulated the world-wide hunt for similar deposits. This volume describes and provides ready access to the literature for all known occurrences of alkaline igneous rocks and carbonatites of Antarctica, Asia and Europe excluding the former USSR, Australasia and oceanic islands. More than 1,200 occurrences from 59 countries are outlined together with those of 57 oceanic islands and island groups. The descriptions include geographical coordinates and information on general geology, rock types, petrography, mineralogy, age and economic aspects with the principal references cited. There are 429 geological and distribution maps and a locality index. As has been demonstrated by the three earlier volumes, the present book is likely to be of considerable interest to mineral exploration companies, as there are no comprehensive published reviews of the economic aspects of the alkaline rocks. It will also interest research scientists in the fields of igneous petrology and volcanology, and geologists concerned with the regional distribution of igneous rocks and their geodynamic relationships.
Abstract: Alkaline igneous rocks and carbonatites are compositionally and mineralogically the most diverse of all igneous rocks and, apart from their scientific interest, are of major, and growing, economic importance. They are valuable repositories of certain metals and commodities - the only significant sources of some of them - and include Nb, the rare earths, Cu, V, diamond, phosphate, vermiculite, bauxite, raw materials for the manufacture of ceramics, and potentially Th and U. The economic potential of these rocks is now widely appreciated, particularly since the commencement of the mining of the Palabora carbonatite for copper and a host of valuable by-products. Similarly, the crucial economic dominance of rare earth production from carbonatite-related occurrences in China has stimulated the world-wide hunt for related deposits. This volume describes and provides ready access to the literature for all known occurrences of alkaline igneous rocks and carbonatites of Antarctica, Asia and Europe (excluding the former USSR), Australasia and the oceanic islands. More than 1200 occurrences from 59 countries are outlined, together with those of 57 oceanic islands and island groups. The descriptions include geographical coordinates and information on general geology, rock types, petrography, mineralogy, age and economic aspects, with the principal references cited. A brief description is also given of alkaline minerals in meteorites and of alkaline rocks on Mars and Venus. There are 429 geological and distribution maps and a locality index. As has been demonstrated by the three earlier volumes, Alkaline Rocks Part 4 is likely to be of considerable interest to mineral exploration companies, as there are no comprehensive published reviews of the economic aspects of the alkaline rocks. It will also interest research scientists in the fields of igneous petrology and volcanology, and geologists concerned with the regional distribution of igneous rocks and their geodynamic relationships.
Abstract: As I was finishing my PhD thesis on the Borralan alkaline complex in Scotland, my professor, Basil King, who published the first account of the Napak carbonatite occurrence in Uganda, proposed that I should apply for a NERC fellowship to investigate the fenites associated with carbonatites of the Chilwa Province in Malawi (Fig. 1). After a successful application, I duly flew out to Malawi and spent three months building an extensive collection of fenites from the very large metasomatic aureoles around the carbonatites of Chilwa Island, Tundulu, and Kangankunde. Back at Bedford College (University of London, UK) I had been working on my fenites for about a year when Brian Sturt, a lecturer in the department, told me that at a council meeting of the Mineralogical Society of Great Britain and Ireland the previous day he had been told by Frank Claringbull that he, Claringbull, was looking for a petrologist to work in the Department of Mineralogy at the British Museum (Natural History), now called the Natural History Museum. I arranged to see Claringbull, was interviewed, and was fortunate enough to be appointed as a petrologist in the department.
Geochimica et Cosmochimica Acta, Vol. 213, pp. 574-592.
Africa, Botswana
deposit - Orapa
Abstract: Major- and trace-element compositions of garnet and clinopyroxene, as well as 87Sr/86Sr in clinopyroxene and ?18O in garnet in eclogite and pyroxenite xenoliths from Orapa, at the western margin of the Zimbabwe craton (central Botswana), were investigated in order to trace their origin and evolution in the mantle lithosphere. Two groups of eclogites are distinguished with respect to 87Sr/86Sr: One with moderate ratios (0.7026-0.7046) and another with 87Sr/86Sr >0.7048 to 0.7091. In the former group, heavy ?18O attests to low-temperature alteration on the ocean floor, while 87Sr/86Sr correlates with indices of low-pressure igneous processes (Eu/Eu?, Mg#, Sr/Y). This suggests relatively undisturbed long-term ingrowth of 87Sr at near-igneous Rb/Sr after metamorphism, despite the exposed craton margin setting. The high-87Sr/86Sr group has mainly mantle-like ?18O and is suggested to have interacted with a small-volume melt derived from an aged phlogopite-rich metasome. The overlap of diamondiferous and graphite-bearing eclogites and pyroxenites over a pressure interval of ?3.2 to 4.9 GPa is interpreted as reflecting a mantle parcel beneath Orapa that has moved out of the diamond stability field, due to a change in geotherm and/or decompression. Diamondiferous eclogites record lower median 87Sr/86Sr (0.7039) than graphite-bearing samples (0.7064) and carbon-free samples (0.7051), suggesting that interaction with the - possibly oxidising - metasome-derived melt caused carbon removal in some eclogites, while catalysing the conversion of diamond to graphite in others. This highlights the role of small-volume melts in modulating the lithospheric carbon cycle. Compared to diamondiferous eclogites, eclogitic inclusions in diamonds are restricted to high FeO and low SiO2, CaO and Na2O contents, they record higher equilibrium temperatures and garnets have mostly mantle-like O isotopic composition. We suggest that this signature was imparted by a sublithospheric melt with contributions from a clinopyroxene-rich source, possibly related to the ca. 2.0 Ga Bushveld event.
Geochimica et Cosmochimica Acta, Vol. 213, 1, pp. 574-592.
Africa, Botswana
deposit - Orapa
Abstract: Major- and trace-element compositions of garnet and clinopyroxene, as well as 87Sr/86Sr in clinopyroxene and ?18O in garnet in eclogite and pyroxenite xenoliths from Orapa, at the western margin of the Zimbabwe craton (central Botswana), were investigated in order to trace their origin and evolution in the mantle lithosphere. Two groups of eclogites are distinguished with respect to 87Sr/86Sr: One with moderate ratios (0.7026-0.7046) and another with 87Sr/86Sr >0.7048 to 0.7091. In the former group, heavy ?18O attests to low-temperature alteration on the ocean floor, while 87Sr/86Sr correlates with indices of low-pressure igneous processes (Eu/Eu?, Mg#, Sr/Y). This suggests relatively undisturbed long-term ingrowth of 87Sr at near-igneous Rb/Sr after metamorphism, despite the exposed craton margin setting. The high-87Sr/86Sr group has mainly mantle-like ?18O and is suggested to have interacted with a small-volume melt derived from an aged phlogopite-rich metasome. The overlap of diamondiferous and graphite-bearing eclogites and pyroxenites over a pressure interval of ?3.2 to 4.9 GPa is interpreted as reflecting a mantle parcel beneath Orapa that has moved out of the diamond stability field, due to a change in geotherm and/or decompression. Diamondiferous eclogites record lower median 87Sr/86Sr (0.7039) than graphite-bearing samples (0.7064) and carbon-free samples (0.7051), suggesting that interaction with the - possibly oxidising - metasome-derived melt caused carbon removal in some eclogites, while catalysing the conversion of diamond to graphite in others. This highlights the role of small-volume melts in modulating the lithospheric carbon cycle. Compared to diamondiferous eclogites, eclogitic inclusions in diamonds are restricted to high FeO and low SiO2, CaO and Na2O contents, they record higher equilibrium temperatures and garnets have mostly mantle-like O isotopic composition. We suggest that this signature was imparted by a sublithospheric melt with contributions from a clinopyroxene-rich source, possibly related to the ca. 2.0 Ga Bushveld event.
Abstract: Nickel is a strongly compatible element in olivine, and thus fractional crystallization of olivine typically results in a concave-up trend on a Fo-Ni diagram. "Ni-enriched" olivine compositions are considered those that fall above such a crystallization trend. To explain Ni-enriched olivine crystals, we develop a set of theoretical and computational models to describe how primitive olivine phenocrysts from a parent (high-Mg, high-Ni) basalt re-equilibrate with an evolved (low-Mg, low-Ni) melt through diffusion. These models describe the progressive loss of Fo and Ni in olivine cores during protracted diffusion for various crystal shapes and different relative diffusivities for Ni and Fe-Mg. In the case when the diffusivity of Ni is lower than that for Fe-Mg interdiffusion, then olivine phenocrysts affected by protracted diffusion form a concave-down trend that contrasts with the concave-up crystallization trend. Models for different simple geometries show that the concavity of the diffusion trend does not depend on the size of the crystals and only weakly depends on their shape. We also find that the effect of diffusion anisotropy on trend concavity is in the same magnitude as the effect of crystal shape. Thus, both diffusion anisotropy and crystal shape do not significantly change the concave-down diffusion trend. Three-dimensional numerical diffusion models using a range of more complex, realistic olivine morphologies with anisotropy corroborate this conclusion. Thus, the curvature of the concave-down diffusion trend is mainly determined by the ratio of Ni and Fe-Mg diffusion coefficients. The initial and final points of the diffusion trend are in turn determined by the compositional contrast between mafic and more evolved melts that have mixed to cause disequilibrium between olivine cores and surrounding melt. We present several examples of measurements on olivine from arc basalts from Kamchatka, and several published olivine datasets from mafic magmas from non-subduction settings (lamproites and kimberlites) that are consistent with diffusion-controlled Fo-Ni behaviour. In each case the ratio of Ni and Fe-Mg diffusion coefficients is indicated to be?
Twenty years at the Ekati diamond mine: corporate social responsibility in action. CSR
2018 Yellowknife Geoscience Forum , p. 47-48. abstract
Canada, Northwest Territories
deposit - Ekati
Abstract: The Ekati Diamond Mine in the Northwest Territories is owned and operated by Dominion Diamond Mines, the largest Canadian independent diamond producer. The Ekati mine was the first diamond mine in Canada, and started production in October 1998. In 2018 the operation is celebrating its twenty year anniversary. In the presentation, we will look back on some of the milestones and achievements of the last two decades. We will also discuss the commitment of the company to make a positive difference in the North through Corporate Social Responsibility initiatives, including support for education, training, community development, business opportunities and respect for the environment. Some examples include:
Community: Whether mining in northern Canada or sorting diamonds in India, we firmly believe that we can - and should - contribute to the social and economic well-being of the communities near our operations. Dominion's Indigenous partners and business operations are important stakeholders and we respect and value their rights, Traditional Knowledge (TK), and cultural heritage.
Hiring, Training and Development: Dominion Diamond Mines is committed to ensuring that the Ekati mine is a welcoming workplace for all employees and that we remain an employer of choice, particularly among northerners and northern Indigenous communities. The company has a number of initiatives and policies to encourage northerners, representatives from Indigenous groups, and women to enter the mining industry. Environment: Throughout the mining process, Dominion Diamond keeps the land and water of the Ekati mine clean and safe for people, plants, and animals. We understand the importance of the Arctic tundra environment and we are committed to mining in the safest, most environmentally responsible way.
Abstract: Plate reconstruction studies show that the Neotethys Ocean was closing due to the convergence of Africa and Eurasia toward the end of the Cretaceous. The period around 75 Ma reflects the onset of continental collision between the two plates as convergence continued to be taken up mostly by subduction of the Neotethys slab beneath Eurasia. The Owen transform plate boundary in the northeast accommodated the fast northward motion of the Indian plate relative to the African plate. The rest of the plate was surrounded by mid-ocean ridges. Africa was experiencing continent-wide rifting related to northeast-southwest extension. We aim to quantify the forces and paleostresses that may have driven this continental extension. We use the latest plate kinematic reconstructions in a grid search to estimate horizontal gravitational stresses (HGSs), plate boundary forces, and the plate's interaction with the asthenosphere. The contribution of dynamic topography to HGSs is based on recent mantle convection studies. We model intraplate stresses and compare them with the strain observations. The fit to observations favors models where dynamic topography amplitudes are smaller than 300 m. The results also indicate that the net pull transmitted from slab to the surface African plate was low. To put this into context, we notice that available tectonic reconstructions show fragmented subduction zones and various colliding micro-continents along the northern margin of the African plate around this time. We therefore interpret a low net pull as resulting from either a small average slab length or from the micro-continents' resistance to subduction.
Natarajam, R., Savitha, G., Dominiak, P., Wozniak, K., Moorthy, J.N.
Corundum, diamond and PtS metal organic frameworks with a difference: self assembly of a unique pair of 3-connecting D2d symmetric 3,3',5,5' tetrakis(4-pyridyl)bimesity1.
Angewandie Chemie, Vol. 44, 14, March 29, pp. 2115-2119.
Journal of Applied Business and Economics, Vol. 15, 3, 12p. Pdf
Global
economics
Abstract: While prospecting by junior mining companies (JMCs) is a vital contributor to modern wealth creation, attributes of the junior mining sector (JMS) limit JMC-fund raisings to external equity (shares). In considering responses by JMC principals to deep discounting and other JMC-investor strategies, potential responses were found to: increase returns to principals, increase JMS moral-hazard issues, and further deepen price discounts on JMC share offerings, especially IPOs. It is suggested that the attractiveness and moral-hazard consequences of these potential responses can be greatly diminished if mining-tenement fees are raised and JMC prospecting costs are allowed as an offset against those fees.
Chemical Geology, DOI:101016/ j.chemgeo.2020.119464
Mantle
peridotite
Abstract: The lithospheric mantle should be depleted in base- and precious-metals as these elements are transferred to the crust during partial melting. However, some melt-depleted mantle peridotites are enriched in these ore-forming elements. This may reflect re-fertilization of the mantle lithosphere and/or sequestering of these elements by residual mantle phase(s). Both processes remain poorly understood because of the low abundances of incompatible elements in peridotite and the nugget-like distribution of digestion-resistant mantle phases that pose analytical challenges for conventional geochemical methods. Herein we report new major and trace element concentrations for a suite of mantle peridotite and pyroxenite samples from the Late Permian to Middle Triassic Nahlin ophiolite (Cache Creek terrane, British Columbia, Canada) using Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICPMS) analysis of nanoparticulate powders and olivine. Compatible to moderately incompatible element concentrations suggest that Nahlin ophiolite peridotites represent residues after ?20% melt extraction. Pyroxenite dykes and replacive dunite bands are folded and closely intercalated with residual harzburgite. These field relationships, coupled with the presence of intergranular base metal sulphide, clinopyroxene and Cr-spinel at the microscale, point to percolating melts that variably re-fertilized melt-depleted mantle peridotite. Radiogenic Pb (206Pb/204Pb?=?15.402-19.050; 207Pb/204Pb?=?15.127-15.633; 208Pb/204Pb?=?34.980-38.434; n?=?45) and Os (187Os/188Os 0.1143-0.5745; n?=?58) isotope compositions for a subset of melt-depleted peridotite samples further support metasomatic re-fertilization of these elements. Other ore-forming elements are also implicated in these metasomatic reactions because some melt-depleted peridotite samples are enriched relative to the primitive mantle, opposite to their expected behaviour during partial melting. New LA-ICPMS analysis of fresh olivine further demonstrates that a significant proportion of the highly incompatible element budget for the most melt-depleted rocks is either hosted by, and/or occurs as trapped inclusions within, the olivine-rich residues. Trapped phases from past melting and/or re-fertilization events are the preferred explanation for unradiogenic Pb isotope compositions and Paleozoic to Paleoproterozoic Re-depletion model ages, which predate the Nahlin ophiolite by over one billion years.
Marine and Petroleum Geology, Vol. 28, pp. 1385-1401.
Africa, South Africa
geomorphology
Abstract: The application of the onset of supercontinentality, the “Great Oxidation Event” (GOE) and the first global scale glaciation in the Neoarchaean-Palaeoproterozoic as panacea-like events providing a framework or even chronological piercing points in Earth’s history at this time, is questioned. There is no solid evidence that the Kaapvaal craton was part of a larger amalgamation at this time, and its glacigenic record is dominated by deposits supporting the operation of an active hydrological cycle in parallel with glaciation, thereby arguing against the “Snowball Earth Hypothesis”. While the Palaeoproterozoic geological record of Kaapvaal does broadly support the GOE, this postulate itself is being questioned on the basis of isotopic data used as oxygen-proxies, and sedimentological data from extant river systems on the craton argue for a prolongation of the greenhouse palaeo-atmosphere (possibly in parallel with a relative elevation of oxygen levels) which presumably preceded the GOE. The possibility that these widespread events may have been diachronous at the global scale is debated.
New Strontium, neodymium, lead isotopic dat a from plutons in the northern Great Basin: implications for crustal structure and granite petrogenesis in the hinterland of the Sevier th
Abstract: Preexisting crustal heterogeneities are shown to influence rift process at a variety of scales. However, our understanding of how crustal inheritance influences rift?scale spatiotemporal kinematics of faulting in magma?poor rift environments is still very limited. Studies of active continental rifts can provide high?fidelity assessments of extensional processes and structures that are not possible through examination of ancient rifts that have undergone subsequent deformation events or are buried deeply beneath passive margins. We examine the influence of crustal inheritance on active rifting through balancing and restoring a series of regional cross sections across the Lake Tanganyika Rift in the Western Branch of the East African Rift System. The cross sections are produced using legacy seismic reflection data, reprocessed through prestack depth migration. This type example of a young, magma?poor continental rift transects several different basement terranes, including an Archean/Paleoproterozoic craton, and Proterozoic mobile belts. The Lake Tanganyika Rift exhibits two classic bell?shaped profiles of extension along strike, reaching a maximum of 7.15 km. A spatiotemporal integration of the extension data, and comparison with the various basement terranes the rift transects, reveals that extension in cratonic blocks is more widely distributed compared to mobile belt terranes, where strain rapidly localizes onto border faults by later rift stages. These results reveal how crustal inheritance exerts a fundamental control on the evolution of extension localization, ultimately impacting the geometry and structural architecture of rift basins.
Abstract: The architecture of subsurface magma plumbing systems influences a variety of igneous processes, including the physiochemical evolution of magma and extrusion sites. Seismic reflection data provides a unique opportunity to image and analyze these subvolcanic systems in three dimensions and has arguably revolutionized our understanding of magma emplacement. In particular, the observation of (1) interconnected sills, (2) transgressive sill limbs, and (3) magma flow indicators in seismic data suggest that sill complexes can facilitate significant lateral (tens to hundreds of kilometers) and vertical (<5 km) magma transport. However, it is often difficult to determine the validity of seismic interpretations of igneous features because they are rarely drilled, and our ability to compare seismically imaged features to potential field analogues is hampered by the limited resolution of seismic data. Here we use field observations to constrain a series of novel seismic forward models that examine how different sill morphologies may be expressed in seismic data. By varying the geologic architecture (e.g., host-rock lithology and intrusion thickness) and seismic properties (e.g., frequency), the models demonstrate that seismic amplitude variations and reflection configurations can be used to constrain intrusion geometry. However, our results also highlight that stratigraphic reflections can interfere with reflections generated at the intrusive contacts, and may thus produce seismic artifacts that could be misinterpreted as real features. This study emphasizes the value of seismic data to understanding magmatic systems and demonstrates the role that synthetic seismic forward modeling can play in bridging the gap between seismic data and field observations.
Journal of Metamorphic Geology, doi.org/10/111/jmg.12566
Mantle
coesite
Abstract: Ultrahigh?pressure (UHP) metamorphism observed in continental terranes implies that continental crust can subduct to ~40 kbar before exhuming to the surface. This process is one of the least understood and widely debated parts of the orogenic cycle. The dominantly felsic composition of UHP continental terranes means that many petrology?based techniques for determining peak pressures and temperatures are often not possible. In such cases, the detection of UHP conditions depends on the preservation of coesite, a rarely preserved mineral in exhumed UHP terranes as it rapidly transforms to quartz on decompression. Consequently, the qualitative identification of palisade quartz microstructures that form during the retrograde transformation of coesite to quartz is often used to identify UHP terranes. In this study, we conduct EBSD and misorientation analysis of palisade quartz inclusions in the coesite?bearing pyrope quartzite from the Dora Maira massif in the Alps, and matrix?scale palisade quartz in the Polokongka La granite from Tso Morari in the Ladakh Himalaya, in order to quantitatively define crystallographic characteristics of quartz after coesite. The repeatability of our observations in two unrelated occurrences of UHP rocks supports our interpretation that the following features provide a systematic and predictable set of criteria to identify the coesite to quartz transition: (1) Quartz crystallographic orientations define spatially and texturally distinct subdomains of palisade quartz grains with ‘single crystal’ orientations defined by distinct c?axis point?maxima. (2) Adjacent subdomains are misorientated with respect to each other by a misorientation angle/axis of 90°/. (3) Within each subdomain, palisade quartz grain boundaries commonly have intra? and inter?granular misorientations of 60°/[0001], consistent with the dauphiné twin law. Our observations imply that the coesite?to?quartz transformation is crystallographically controlled by the epitaxial nucleation of palisade quartz on the former coesite grain, specifically on potential coesite twin planes such as (101) and (021).
Geochronology and geochemistry of felsic xenoliths in lamprophyre dikes from the southeastern margin of the North Chin a Craton: implications for the interleaving of the Dabie Sulu orogenic crust.
International Geology Review, Vol. 57, 9-10, pp. 1305-1325.
Abstract: A new data compilation shows that in intermediate to felsic rocks, zircon Eu/Eu* [chondrite normalized Eu/ graphic] correlates with whole rock La/Yb, which has been be used to infer crustal thickness. The resultant positive correlation between zircon Eu/Eu* and crustal thickness can be explained by two processes favored during high-pressure differentiation: (1) supression of plagioclase and (2) endogenic oxidation of Eu2+ due to garnet fractionation. Here we calibrate a crustal thickness proxy based on Eu anomalies in zircons. The Eu/Eu*-in-zircon proxy makes it possible to reconstruct crustal thickness evolution in magmatic arcs and orogens using detrital zircons. To evaluate this new proxy, we analyzed detrital zircons separated from modern river sands in the Gangdese belt, southern Tibet. Our results reveal two episodes of crustal thickening (to 60-70 km) since the Cretaceous. The first thickening event occurred at 90-70 Ma, and the second at 50-30 Ma following Eurasia-India collision. These findings are temporally consistent with contractional deformation of sedimentary strata in southern Tibet.
Abstract: Carbonatite represents a major host rock for niobium (Nb) resources worldwide. Both magmatic and post-magmatic metasomatic processes are crucial for Nb mineralization in carbonatites. However, the roles of these metasomatic processes are difficult to be evaluated due to their multiple origins and complexity of the physico-chemical conditions. In this study, we present detailed mineralogical investigations of pyrochlore group minerals and chemical U-Th-Pb geochronology of uraninite within the Miaoya carbonatite complex, aiming to better characterize the role of post-magmatic metasomatic events. The Miaoya complex (ca. 420-440?Ma) hosts the second largest carbonatite-related Nb deposit in China, mainly in the form of pyrochlore group minerals, ferrocolumbite and Nb-bearing rutile. Primary pyrochlore group minerals evolved from pyrochlore to uranpyrochlore, and ultimately reaching the betafite end-member during the magmatic stage. They have then experienced an episode of metasomatic events at 235.4?±?4.1?Ma, as determined by U-Th-Pb chemical ages of secondary uraninite. Fluids activity for uranpyrochlore alteration was concomitant with the hydrothermal reworking of REE mineralization, which was probably related to tectono-thermal events that occurred during the Triassic closure of the ancient Mianlue Ocean. During this process, hydration and decomposition of uranpyrochlore were characterized by the leaching of Na, Ca and F from its structure, the incorporation of Fe, Si, Sr and Ba from the fluids, and the final in situ replacement by secondary ferrocolumbite, uraninite and Nb-bearing rutile. In addition, parts of Nb and U liberated from uranpyrochlore by metamictization were then transported over distances of several hundreds of microns in relatively reducing (Fe, Si, S, CO2)-bearing fluids under high temperature, and were ultimately re-precipitated in amorphous Fe-Si-U-Nb-bearing oxide veins and poorly crystallized Nb-Ti-Ca-Fe-rich oxides. The relatively weak fluids activity failed to efficiently promote the Nb re-enrichment.
Abstract: Porphyritic olivine kimberlitic breccia, discovered in the Dörbed Banner of Inner Mongolia, Western China, is referred to as Longtou Shan Kimberlite in our study. This kimberlite occurs as a pipe in the Halahuogete Formation of Bayan Obo Group. Zircon U–Pb ages of Longtou Shan Kimberlite reveals a Mesoproterozoic age of ~1,552 Ma, constraining the deposition age of Halahuogete Formation to the Mesoproterozoic. Compared with Mesoproterozoic kimberlite of the ancient landmass, it can be inferred that the North China Craton is a member of the Ur ancient continent of the Columbia supercontinent. Furthermore, according to the tectonic background of the Bayan Obo Group, we raise this possibility that “Bayan Obo Aulacogen” should be renamed the “Bayan Obo Continental Rift.”
Abstract: Porphyritic olivine kimberlitic breccia, discovered in the Dörbed Banner of Inner Mongolia, Western China, is referred to as Longtou Shan Kimberlite in our study. This kimberlite occurs as a pipe in the Halahuogete Formation of Bayan Obo Group. Zircon U-Pb ages of Longtou Shan Kimberlite reveals a Mesoproterozoic age of ~1,552 Ma, constraining the deposition age of Halahuogete Formation to the Mesoproterozoic. Compared with Mesoproterozoic kimberlite of the ancient landmass, it can be inferred that the North China Craton is a member of the Ur ancient continent of the Columbia supercontinent. Furthermore, according to the tectonic background of the Bayan Obo Group, we raise this possibility that “Bayan Obo Aulacogen” should be renamed the “Bayan Obo Continental Rift.”
Abstract: The newly-discovered supergiant Huayangchuan uranium (U)-polymetallic deposit is situated in the Qinling Orogen, Central China. The deposit contains economic endowments of U, Nb, Pb, Se, Sr, Ba and REEs, some of which (e.g., U, Se, and Sr) reaching super-large scale. Pyrochlore, allanite, monazite, barite-celestite and galena are the major ore minerals at Huayangchuan. Uranium is mainly hosted in the primary mineral of pyrochlore, and the mineralization is mainly hosted in or associated with carbonatite dikes. According to the mineral assemblages and crosscutting relationships, the alteration/mineralization at Huayangchuan comprises four stages, i.e., pegmatite REE mineralization (I), main mineralization (II), skarn mineralization (III) and post-ore alteration (IV). Coarse-grained euhedral allanite is the main Stage I REE mineral, and the pegmatite-hosted REE mineralization (ca. 1.8 Ga) occurs mostly in the shallow-level of northwestern Huayangchuan, corresponding to the Paleoproterozoic Xiong'er Group volcanic rocks (1.80-1.75 Ga) in the southern margin of North China Block. Carbonatite-hosted Stage II mineralization contributes to the majority of U-Nb-REE-Ba-Sr resources, and is controlled by the Huayangchuan Fault. Stage II mineralization can be further divided into the sulfate mineralization (barite-celestite) (II-A), alkali-rich U mineralization (aegirine-augite + pyrochlore + uraninite + uranothorite) (II-B) and REE (allanite + monazite + chevkinite)-U (pyrochlore + uraninite) mineralization (II-C) substages. Stage II mineralization may have occurred during the Late Triassic Mianlue Ocean closure. Skarn mineralization contributed to the majority of Pb and minor U-REE (uraninite-allanite) resources at Huayangchuan, and is spatially associated with the Late Cretaceous-Early Jurassic (Yanshanian) Huashan and Laoniushan granites. We suggested that hydrothermal fluids derived from the Laoniushan and Huashan granites may have reacted with the Triassic carbonatites, and formed the Huayangchuan Pb skarn mineralization. The mantle-derived Triassic carbonatites may have been fertilized by the U-rich subducting oceanic sediments, and were further enriched through reacting with the Proterozoic U-REE-rich pegmatite wallrocks at Huayangchuan. Ore-forming elements were likely transported in metal complexes (F?, and ), and deposited with the dilution of the complex concentration. This may have formed the distinct vertical mineralization zoning, i.e., sodic fenite-related alkali-U mineralization at depths and potassic fenite-related REE-U mineralization at shallow level.
Abstract: The newly-discovered supergiant Huayangchuan uranium (U)-polymetallic deposit is situated in the Qinling Orogen, Central China. The deposit contains economic endowments of U, Nb, Pb, Se, Sr, Ba and REEs, some of which (e.g., U, Se, and Sr) reaching super-large scale. Pyrochlore, allanite, monazite, barite-celestite and galena are the major ore minerals at Huayangchuan. Uranium is mainly hosted in the primary mineral of pyrochlore, and the mineralization is mainly hosted in or associated with carbonatite dikes. According to the mineral assemblages and crosscutting relationships, the alteration/mineralization at Huayangchuan comprises four stages, i.e., pegmatite REE mineralization (I), main mineralization (II), skarn mineralization (III) and post-ore alteration (IV). Coarse-grained euhedral allanite is the main Stage I REE mineral, and the pegmatite-hosted REE mineralization (ca. 1.8 Ga) occurs mostly in the shallow-level of northwestern Huayangchuan, corresponding to the Paleoproterozoic Xiong'er Group volcanic rocks (1.80-1.75 Ga) in the southern margin of North China Block. Carbonatite-hosted Stage II mineralization contributes to the majority of U-Nb-REE-Ba-Sr resources, and is controlled by the Huayangchuan Fault. Stage II mineralization can be further divided into the sulfate mineralization (barite-celestite) (II-A), alkali-rich U mineralization (aegirine-augite + pyrochlore + uraninite + uranothorite) (II-B) and REE (allanite + monazite + chevkinite)-U (pyrochlore + uraninite) mineralization (II-C) substages. Stage II mineralization may have occurred during the Late Triassic Mianlue Ocean closure. Skarn mineralization contributed to the majority of Pb and minor U-REE (uraninite-allanite) resources at Huayangchuan, and is spatially associated with the Late Cretaceous-Early Jurassic (Yanshanian) Huashan and Laoniushan granites. We suggested that hydrothermal fluids derived from the Laoniushan and Huashan granites may have reacted with the Triassic carbonatites, and formed the Huayangchuan Pb skarn mineralization. The mantle-derived Triassic carbonatites may have been fertilized by the U-rich subducting oceanic sediments, and were further enriched through reacting with the Proterozoic U-REE-rich pegmatite wallrocks at Huayangchuan. Ore-forming elements were likely transported in metal complexes (F?, and ), and deposited with the dilution of the complex concentration. This may have formed the distinct vertical mineralization zoning, i.e., sodic fenite-related alkali-U mineralization at depths and potassic fenite-related REE-U mineralization at shallow level.
Abstract: The time and processes of hydrothermal mineralization are long-standing problems in geology. This work addresses these questions with reference to the Maoniuping giant rare earth elements (REE) deposit (southwest China), which has rare earth oxides (REO) reserves of 3.17 million tons with an average grade of 2.95 wt%. Bastnäsite is the dominant economic mineral, occurring as four distinct paragenetic types in the Maoniuping syenite-carbonatite complex: (1) primary euhedral bastnäsite (type-A) in syenite, with isolated melt inclusions; (2) macro-crystalline tabular euhedral bastnäsite (type-B) in pegmatitic dikes, with a diverse variety of fluid inclusions; (3) fine-grained, anhedral veinlet-disseminated bastnäsite (type-C) in syenite; and (4) coarse-grained anhedral bastnäsite (type-D) in carbonatite dikes, occurring as veinlets or interstitial to calcite, fluorite, and barite. From the paragenetic and compositional variations, it is inferred that type-A bastnäsite is of primary magmatic origin, whereas the other three types have characteristics of hydrothermal origins. In situ LA-ICP-MS U-Pb geochronology of the four types of bastnäsite results in lower intercept ages of 28.2 ± 0.5 Ma (n = 95, MSWD = 5.10), 27.8 ± 0.4 Ma (n = 43, MSWD = 0.73), 26.8 ± 0.7 Ma (n = 50, MSWD = 0.83), and 25.8 ± 0.7 Ma (n = 55, MSWD = 1.70), respectively, which are consistent with the weighted average 206Pb/238U and 208Pb/232Th ages by 207Pb-correction method. Compositional variations of clinopyroxene and apatite from the associated syenite, pegmatitic and carbonatitic dikes indicate a genetic relationship of the Maoniuping alkaline complex. The compositions of clinopyroxene range from Ae44-67Di14-18Hd17-41 in pegmatitic dikes, Ae43-66Di6-20Hd21-38 in carbonatitic dikes to Ae68-90Di0-3Hd10-30 in syenite. Apatites in the pegmatitic and carbonatitic dikes have similar compositions with higher F, total REE, and Sr, and lower CaO contents than those in the syenite, which suggests a cogenetic origin for the associated pegmatite and carbonatite. Clinopyroxene and apatite compositions suggest that the pegmatitic melt might differentiate directly from the initial carbonatitic melt rather than the syenitic magma. The bastnäsite U-Pb geochronology and minerals data indicate continuous magmatic-hydrothermal evolution for the REE mineralization in the Maoniuping alkaline complex.
Abstract: Comprehensive studies of zircon xenocrysts from kimberlites of the Kuoika field (northeastern Siberian craton) and several kimberlite fields of the eastern Anabar shield, along with data compilation on the age of kimberlite-hosting terranes, reveal details of the evolution of the northern Siberian craton. The age distribution and trace element characteristic of zircons from the Kuoika field kimberlites (Birekte terrane) provide evidence of significant basic and alkaline-carbonatite magmatism in northern Siberia in the Paleozoic and Mesozoic periods. The abundance of 1.8-2.1 Ga zircons in both the Birekte and adjacent Hapchan terranes (the latter hosting kimberlites of the eastern Anabar shield) supports the Paleoproterozoic assembly and stabilization of these units in the Siberian craton and the supercontinent Columbia. The abundance of Archean zircons in the Hapchan terrane reflects the input of an ancient source other than the Birekte terrane and addresses the evolution of the terrane to west (Magan and Daldyn terranes of the Anabar shield). The present study has also revealed the oldest known remnant of the Anabar shield crust, whose 3.62 Ga age is similar to that of the other ancient domain of Siberia, the Aldan shield. The first Hf isotope data for the Anabar shield coupled with the U-Pb systematics indicate three stages of crustal growth (Paleoproterozoic, Neoarchean and Paleoarchean) and two stages of the intensive crustal recycling in the Paleoproterozoic and Neoarchean. Intensive reworking of the existing crust at 2.5-2.8 Ga and 1.8-2.1 Ga is interpreted to provide evidence for the assembly of Columbia. The oldest Hf model age estimation provides a link to Early Eoarchean (3.7-3.95 Ga) and possibly to Hadean crust. Hence, some of the Archean cratonic segments of the Siberian craton could be remnants of the Earth's earliest continental crust.
International Journal of Earth Sciences, Vol. 106, 7, pp. 2233-2257.
China
craton
Abstract: Craton destruction is a dynamic event that plays an important role in Earth’s evolution. Based on comprehensive observations of many studies on the North China Craton (NCC) and correlations with the evolution histories of other cratons around the world, craton destruction has be defined as a geological process that results in the total loss of craton stability due to changes in the physical and chemical properties of the involved craton. The mechanisms responsible for craton destruction would be as the follows: (1) oceanic plate subduction; (2) rollback and retreat of a subducting oceanic plate; (3) stagnation and dehydration of a subducting plate in the mantle transition zone; (4) melting of the mantle above the mantle transition zone caused by dehydration of a stagnant slab; (5) non-steady flow in the upper mantle induced by melting, and/or (6) changes in the nature of the lithospheric mantle and consequent craton destruction caused by non-steady flow. Oceanic plate subduction itself does not result in craton destruction. For the NCC, it is documented that westward subduction of the paleo-Pacific plate should have initiated at the transition from the Middle-to-Late Jurassic, and resulted in the change of tectonic regime of eastern China. We propose that subduction, rollback and retreat of oceanic plates and dehydration of stagnant slabs are the main dynamic factors responsible for both craton destruction and concentration of mineral deposits, such as gold, in the overriding continental plate. Based on global distribution of gold deposits, we suggest that convergent plate margins are the most important setting for large gold concentrations. Therefore, decratonic gold deposits appear to occur preferentially in regions with oceanic subduction and overlying continental lithospheric destruction/modification/growth.
Isotopic constraints on age and duration of fluid assisted high pressure eclogite facies recrystallization during exhumation of deeply subducted continental crurs
Journal of Metamorphic Geology, Vol. 24, 8, pp. 687-702.
Precisely dating Paleozoic kimberlites in the North Chin a craton and Hf isotopic constraints on the evolution of the subcontinental lithospheric mantle.
Precise age determin ation of the Paleozoic kimberlites in North Chin a craton and Hf isotopic constraint on the evolution of its subcontinental lithospheric mantle.
Guarino, V., Wu, F-Y., Lustrino, M., Melluso, L.,Brotzu, P., De Barros Gomes, C., Ruberti, E., Tassarini, C.C.G., Svisero, D.P.
U Pb ages, Sr Nd isotope geochemistry, and petrogenesis of kimberlites, kamafugites and phlogopite picrites of the Alto Paranaiba Igneous Province, Brazil.
Mesoproterozoic U-Pb ages, trace element and Sr-Nd isotopic composition of perovskite from kimberlites of the Eastern Dharwar craton, southern India: distinct mantle sources and a Wide spread 1.1 Ga Tectonomagmatic event.
Guarino, V., Wu, F-Y., Lustrino, M., Melluso, L., Brotzu, P., Barros Gomes, C.de, Ruberti, E., Tassarini, C.C.G., Svisero, D.P.
U-Pb ages, Sr, Nd isotope geochemistry, and petrogenesis of kimberlites, kamafugites and phlogopte-picrites of the Alto Paranaiba Igneous Province, Brazil.
Repeated kimberlite magmatism beneath Yakutia and its relationship to Siberian flood volcanism: insights from in situ U-Pb and Sr-Nd perovskite isotope analysis.
Earth and Planetary Science Letters, Vol. 404, Oct. pp. 283-295.
Abstract: We report groundmass perovskite U -Pb (SIMS) ages, perovskite Nd isotopic (LA-ICPMS) composition and bulk-rock geochemical data of the Timmasamudram diamondiferous kimberlite cluster, Wajrakarur kimberlite field, in the Eastern Dharwar craton of southern India. The kimberlite pipes gave similar Mesoproterozoic ages of 1086 ± 19 Ma (TK-1, microcrystic variant) and 1119 ± 12 Ma (TK-3). However, a perovskite population sampled from the macrocrystic variant of TK-1 gave a much younger Late Cretaceous age of ca. 90 Ma. This macrocrystic kimberlite phase intrudes the Mesoproterozoic microcrystic phase and has a distinct bulk-rock geochemistry. The Nd-isotope composition of the ~ 1100 Ma perovskites in the cluster show depleted ?Nd(T) values of 2.1 ± 0.6 to 6.7 ± 0.3 whereas the ~ 90 Ma perovskites have enriched ?Nd(T) values of ? 6.3 ± 1.3. The depleted-mantle (DM) model age of the Cretaceous perovskites is 1.2 Ga, whereas the DM model age of the Proterozoic perovskites is 1.2 to 1.5 Ga. Bulk-rock incompatible trace element ratios (La/Sm, Gd/Lu, La/Nb and Th/Nb) of all Timmasamudram kimberlites show strong affinity with those from the Cretaceous Group II kimberlites from the Bastar craton (India) and Kaapvaal craton (southern Africa). As the Late Cretaceous age of the younger perovskites from the TK-1 kimberlite is indistinguishable from that of the Marion hotspot-linked extrusive and intrusive igneous rocks from Madagascar and India, we infer that all may be part of a single Madagascar Large Igneous Province. Our finding constitutes the first report of Cretaceous kimberlite activity from southern India and has significant implications for its sub-continental lithospheric mantle evolution and diamond exploration programs.
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680-540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241-0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400-km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078-0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680-540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241-0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400 km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078-0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
Abstract: Alkaline rock and carbonatite complexes, including the Prairie Lake complex (NW Ontario), are widely distributed in the Canadian region of the Midcontinent Rift in North America. It has been suggested that these complexes were emplaced during the main stage of rifting magmatism and are related to a mantle plume. The Prairie Lake complex is composed of carbonatite, ijolite and potassic nepheline syenite. Two samples of baddeleyite from the carbonatite yield U-Pb ages of 1157.2±2.3 and 1158.2±3.8 Ma, identical to the age of 1163.6±3.6 Ma obtained for baddeleyite from the ijolite. Apatite from the carbonatite yields the same U-Pb age of ~1160 Ma using TIMS, SIMS and laser ablation techniques. These ages indicate that the various rocks within the complex were synchronously emplaced at about 1160 Ma. The carbonatite, ijolite and syenite have identical Sr, Nd and Hf isotopic compositions with a 87Sr/86Sr ratio of ~0.70254, and positive ?Nd(t)1160 and ?Hf(t)1160 values of ~+3.5 and ~+4.6, respectively, indicating that the silicate and carbonatitic rocks are co-genetic and related by simple fractional crystallization from a magma derived from a weakly depleted mantle. These age determinations extend the period of magmatism in the Midcontinent Rift in the Lake Superior area to 1160 Ma, but do not indicate whether the magmatism is associated with passive continental rifting or the initial stages of plume-induced rifting.
Abstract: Apatites from the Verity, Fir, Gum, Howard Creek and Felix carbonatites of the Blue River (British Columbia, Canada) area have been investigated with respect to their paragenesis, cathodoluminescence, trace element and Sr–Nd isotopic composition. Although all of the Blue River carbonatites were emplaced as sills prior to amphibolite grade metamorphism and have undergone deformation, in many instances magmatic textures and mineralogy are retained. Attempts to constrain the U–Pb age of the carbonatites by SIMS, TIMS and LA–ICP-MS studies of zircon and titanite were inconclusive as all samples investigated have experienced significant Pb loss during metamorphism. The carbonatites are associated with undersaturated calcite–titanite amphibole nepheline syenite only at Howard Creek although most contain clasts of disaggregated phoscorite-like rocks. Apatite from each intrusion is characterized by distinct, but wide ranges, in trace element composition. The Sr and Nd isotopic compositions define an array on a 87Sr/86Sr vs²Nd diagram at 350 Ma indicating derivation from depleted sub-lithospheric mantle. This array could reflect mixing of Sr and Nd derived from HIMU and EM1 mantle sources, and implies that depleted mantle underlies the Canadian Cordillera. Although individual occurrences of carbonatites in the Blue River region are mineralogically and geochemically similar they are not identical and thus cannot be considered as rocks formed from a single batch of parental magma at the same stage of magmatic evolution. However, a common origin is highly probable. The variations in the trace element content and isotopic composition of apatite from each occurrence suggest that each carbonatite represents a combination of derivation of the parental magma(s) from mineralogically and isotopically heterogeneous depleted mantle sources coupled with different stages of limited differentiation and mixing of these magmas. We do not consider these carbonatites as primary direct partial melts of the sub-lithospheric mantle which have ascended from the asthenosphere without modification of their composition.
Abstract: Neoproterozoic kimberlite, ultramafic lamprophyre, and carbonatite magmatic activity was widespread across the Canadian-Greenland Shield. Models to explain the preponderance of this deeply-derived CO2-rich magmatism between 680–540 Ma range from impingement of multiple mantle plumes to rifting activity linked to the breakout of the Laurentian plate from the Rodinia supercontinent configuration. We add to the debate about the origin of kimberlite magmas and evaluate possible mantle sources of the 655 Ma ‘diamond-rich’ Renard (new SIMS U/Pb perovskite ages) and 629 Ma ‘barren’ Wemindji kimberlites on the eastern Superior craton in Quebec, Canada. Our Sr-Nd-Hf and carbon isotope data (87Sr/86Sri = 0.70241–0.70442; ?Ndi = + 0.2 to + 4.8; ?Hfi = + 0.3 to + 6.5; ?13C = ? 5.6 to ? 3.9‰) suggest a common and moderately depleted convecting upper mantle source region for both the Renard and Wemindji kimberlites, which occur 400 km apart in the interior of the Superior craton. In contrast, the low Os isotope ratios (187Os/188Osi = 0.11078–0.12620; ?Osi = ? 13.7 to ? 1.6) and unfractionated chondritic relative HSE abundances (Os, Ir, Ru, Pt, Pd, Re) indicate significant involvement of ancient refractory cratonic mantle material in kimberlite magma formation. Our model calculations suggest that for both the diamond-rich Renard and the barren Wemindji kimberlite magmas up to 30% of the Os was derived from refractory cratonic peridotites. This material might have been assimilated by originally more CO2-rich carbonated silicate melts derived from the asthenosphere. We also show that the geochemical and Sr-Nd-Hf-Os isotopic compositions of the Renard and Wemindji kimberlites do not require significant input from melts derived from olivine-poor cratonic mantle lithologies such as MARID-type veins and pyroxenites/eclogites. This contrasts with the petrogenesis of deeply-derived volatile-rich potassic magmas found along the peripheries of cratons (e.g., ultramafic lamprophyres, kamafugites, and olivine lamproites), a setting where abundant non-peridotitic components have been added to the lithospheric mantle over the course of continent evolution. Provided that CO2-rich melts, such as proto-kimberlites, occur near the solidus of volatile-fluxed peridotites, no excess mantle heat is required in their formation. This important but often overlooked constraint, together with the observation that there exist no spatial or temporal relationships between the Superior craton kimberlites and Large Igneous Provinces during the Late Neoproterozoic, suggests that kimberlite magmatic activity was tectonically controlled. In our preferred model, ubiquitous CO2-rich proto-kimberlite melts form during volatile-controlled redox melting processes at ambient mantle temperatures in a thermal boundary layer directly beneath thick cratonic lithosphere. The success rate of ‘evolving’ hybrid kimberlite magmas reaching Earth’s surface increases when tensile stresses propagate into the > 200 km thick keels of continental lithosphere. These conditions are frequently met during fast and changing plate motions associated with the assembly and breakup of supercontinents.
International Journal of Earth Sciences, Vol. 106, 6, pp. 1963-1989.
South America, Brazil
carbonatite - Catalao II
Abstract: The Catalão II carbonatitic complex is part of the Alto Paranaíba Igneous Province (APIP), central Brazil, close to the Catalão I complex. Drill-hole sampling and detailed mineralogical and geochemical study point out the existence of ultramafic lamprophyres (phlogopite-picrites), calciocarbonatites, ferrocarbonatites, magnetitites, apatitites, phlogopitites and fenites, most of them of cumulitic origin. U–Pb data have constrained the age of Catalão I carbonatitic complex between 78 ± 1 and 81 ± 4 Ma. The initial strontium, neodymium and hafnium isotopic data of Catalão II (87Sr/86Sri= 0.70503–0.70599; ?Ndi= ?6.8 to ?4.7; 176Hf/177Hf = 0.28248–0.28249; ?Hfi= ?10.33 to ?10.8) are similar to the isotopic composition of the Catalão I complex and fall within the field of APIP kimberlites, kamafugites and phlogopite-picrites, indicating the provenance from an old lithospheric mantle source. Carbon isotopic data for Catalão II carbonatites (?13C = ?6.35 to ?5.68 ‰) confirm the mantle origin of the carbon for these rocks. The origin of Catalão II cumulitic rocks is thought to be caused by differential settling of the heavy phases (magnetite, apatite, pyrochlore and sulphides) in a magma chamber repeatedly filled by carbonatitic/ferrocarbonatitic liquids (s.l.). The Sr–Nd isotopic composition of the Catalão II rocks matches those of APIP rocks and is markedly different from the isotopic features of alkaline-carbonatitic complexes in the southernmost Brazil. The differences are also observed in the lithologies and the magmatic affinity of the igneous rocks found in the two areas, thus demonstrating the existence of regional-scale heterogeneity in the mantle sources underneath the Brazilian platform.
Abstract: The characteristics of the sub-continental lithospheric mantle (SCLM) post-date the Siberian plume event (250 Ma) is still unclear; nearly all published data for mantle xenoliths are from a single kimberlite erupt before he Siberian plume (Udachnaya). We report major elements of the whole rock, trace elements data of clinopyroxene and Re-Os isotope and PGE concentration of mantle xenoliths from the Obnazhennaya kimberlite pipe (160 Ma). The Obnazhennaya mantle xenoliths, including spinel harzburgites, spinel dunites, spinel lherzolites, spinel-garnet lherzolite. The spinel harzburgites and dunites have refractory compositions, with 0.23-1.35 wt.% Al2O3, 0.41-3.11 wt.% CaO and 0.00-0.09 wt.% TiO2. Clinopyroxenes in harzburgites and dunites have lower Na2O but higher Cr2O3 contents. Modeling of the Y and Yb contents in clinopyroxenes indicates that the spinel harzburgites and dunites have been subjected to ca. 12-17% degrees of partial melting. The spinel harzburgites and dunites have 187Os/188Os of 0.11227-0.11637, giving a TRD age of 1.6-2.2 Ga. This suggests that old cratonic mantle still existed beneath the Obnazhennaya. In contrast, the lherzolites (both spinel- and spinel-garnet-) have more fertile compositions, containing 2.16-6.55 wt.% Al2O3, 2.91-7.55 wt.% CaO and 0.04-0.15 wt.% TiO2. Both spinel and spinelgarnet lherzolites have more radiogenic 187Os/188Os ratios (0.11931-0.17627), enriched P-PGEs. The higher Al2O3 and Os content and depleted IPGE character of these lherzolites suggest that they were not juvenile mantle accreted by Siberian mantle plume but the refertilized ancient mantle. Therefore, our result suggest that the cratonic mantle beneath the Obnazhennaya has not been replaced by juvenile mantle during the Siberian mantle plume.
Abstract: The characteristics of the sub-continental lithospheric mantle (SCLM) post-date the Siberian plume event (250 Ma) is still unclear; nearly all published data for mantle xenoliths are from a single kimberlite erupt before he Siberian plume (Udachnaya). We report major elements of the whole rock, trace elements data of clinopyroxene and Re-Os isotope and PGE concentration of mantle xenoliths from the Obnazhennaya kimberlite pipe (160 Ma). The Obnazhennaya mantle xenoliths, including spinel harzburgites, spinel dunites, spinel lherzolites, spinel-garnet lherzolite. The spinel harzburgites and dunites have refractory compositions, with 0.23-1.35 wt.% Al2O3, 0.41-3.11 wt.% CaO and 0.00-0.09 wt.% TiO2. Clinopyroxenes in harzburgites and dunites have lower Na2O but higher Cr2O3 contents. Modeling of the Y and Yb contents in clinopyroxenes indicates that the spinel harzburgites and dunites have been subjected to ca. 12-17% degrees of partial melting. The spinel harzburgites and dunites have 187Os/188Os of 0.11227-0.11637, giving a TRD age of 1.6-2.2 Ga. This suggests that old cratonic mantle still existed beneath the Obnazhennaya. In contrast, the lherzolites (both spinel- and spinel-garnet-) have more fertile compositions, containing 2.16-6.55 wt.% Al2O3, 2.91-7.55 wt.% CaO and 0.04-0.15 wt.% TiO2. Both spinel and spinelgarnet lherzolites have more radiogenic 187Os/188Os ratios (0.11931-0.17627), enriched P-PGEs. The higher Al2O3 and Os content and depleted IPGE character of these lherzolites suggest that they were not juvenile mantle accreted by Siberian mantle plume but the refertilized ancient mantle. Therefore, our result suggest that the cratonic mantle beneath the Obnazhennaya has not been replaced by juvenile mantle during the Siberian mantle plume.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links.Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links. Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Journal of Analytical At. Spectrometry, Vol. 33, pp. 231-239.
United States, Arkansas, China, Hebei, Russia, Kola Peninsula, Europe, Sweden, Canada, Ontario
geochronology
Abstract: We report the first U-Pb geochronological investigation of schorlomite garnet from carbonatite and alkaline complexes and demonstrate its applicability for U-Pb age determination using laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS) due to its relatively high U and Th abundances and negligible common Pb content. The comparative matrix effects of laser ablation of zircon and schorlomite are investigated and demonstrate the necessity of a suitable matrix-matched reference material for schorlomite geochronology. Laser-induced elemental fractional and instrumental mass discrimination were externally-corrected using an in house schorlomite reference material (WS20) for U-Pb geochronology. In order to validate the effectiveness and robustness of our analytical protocol, we demonstrate the veracity of U-Pb age determination for five schorlomite samples from: the Magnet Cove complex, Arkansas (USA); the Fanshan ultrapotassic complex, Hebei (China); the Ozernaya alkaline ultramafic complex, Kola Peninsula (Russia); the Alnö alkaline-rock carbonatite complex (Sweden); and the Prairie Lake carbonatite complex, Ontario (Canada). The schorlomite U-Pb ages range from 96 Ma to 1160 Ma, and are almost identical to ages determined from other accessory minerals in these complexes and support the reliability of our analytical protocol. Schorlomite garnet U-Pb geochronology is considered to be a promising new technique for understanding the genesis of carbonatites, alkaline rocks, and related rare-metal deposits.
Abstract: Volcanic pipes, or maar-diatreme volcanoes, form during explosive eruptions of mantle-derived magmas near Earth's surface. Impressive examples are the carrot-shaped, downward tapering structures formed by kimberlite magmas. Kimberlites originate from >150 km depth within Earth's mantle beneath thick continental roots, away from tectonic plate margins. Kimberlite pipes can be significant diamond deposits, and the complex architecture revealed during exploration and mining is ascribed to repeated magma injections leading to multiple eruptions. Repeated magmatic pulses cause diatremes to widen and grow downward, forming kilometer-sized subterranean structures. However, the time-resolved evolution of kimberlite pipe systems is largely unknown. We present the first U/Pb perovskite ages for newly discovered kimberlite dikes (1139.8 ± 4.8 Ma) that cut through the volcaniclastic infill of the Premier kimberlite pipe (1153.3 ± 5.3 Ma) at Cullinan Diamond Mine, South Africa. The ages reveal that renewed kimberlite volcanic activity occurred, at a minimum, 3 m.y. after the main pipe formation. This finding suggests that the largest kimberlite pipes, and maar-diatreme volcanoes in general, may be magmatically active for several millions of years, which conflicts with this volcanism being described as 'monogenetic' at millennia time scales. Exemplified by Tier-1 diamond deposits on the Kaapvaal craton, long-lasting kimberlite volcanic activity may be an important factor in growing large diatremes, plus enabling effective transport of mantle cargo from the diamond stability field to Earth's surface.
Abstract: Zircon xenocrysts from the kimberlites offer a unique opportunity to identify the cryptic basement components hidden in the deep crust and thus to image lithospheric structure and crustal evolution. Zircon xenocrysts from the Triassic kimberlites, exposed in the Rangrim massif of North Korea, were selected for in situ U-Pb and Hf analyses. These zircon xenocrysts are all crust-derived. Their U-Pb age spectrum is characterized by one prominent age population at ca. 1.9-1.8 Ga without any Archean ages, indicating a Paleoproterozoic-dominated basement in the depth of the Rangrim massif. Archean basement should be very limited or absent at depth. This is different with the previous thought of the Rangrim massif being an Archean terrane. However, most of those Paleoproterozoic zircons display negative ?Hf(t) values (-9.7~+0.7) with the average Hf model age of 2.83 ± 0.09 Ga (2?), implying that protoliths of those zircons were not juvenile but derived from reworking of the pre-existed Archean basement. These observations argue for a strong crustal reworking event occurred in the Rangriam massif during Paleoproterozoic, which exhausted most of the preexisted Archean basement rocks and generated a large abundance of Paleoproterozoic rocks. The 1.9~1.8 Ga thermal event has been well documented in the adjacent Jiao- Liao-Ji orogenic belt of the North China Craton. Both of them are characterized by the widely distributed 1.9~1.8 Ga magmatism and share similar igneous rock assemblage. We suggest that the Rangrim massif may be the eastern extension of the Jiao-Liao-Ji belt in North Korea, constituting part of a huge Paleoproterozoic orogen in the eastern margin of the Sino-Korean craton.
Geostandards and Geoanalytical Research, http://orchid.org/0000-0002-2701-4635 80p.
Asia, Sri Lanka
geochronology
Abstract: Here we document a detailed characterization of two zircon gemstones, GZ7 and GZ8. Both stones had the same mass at 19.2 carats (3.84 g) each; both came from placer deposits in the Ratnapura district, Sri Lanka. The U-Pb data are in both cases concordant within the uncertainties of decay constants and yield weighted mean ²??Pb/²³?U ages (95% confidence uncertainty) of 530.26 Ma ± 0.05 Ma (GZ7) and 543.92 Ma ± 0.06 Ma (GZ8). Neither GZ7 nor GZ8 have been subjected to any gem enhancement by heating. Structure?related parameters correspond well with the calculated alpha doses of 1.48 × 10¹? g?¹ (GZ7) and 2.53 × 10¹? g?¹ (GZ8), respectively, and the (U-Th)/He ages of 438 Ma ± 3 Ma (2s) for GZ7 and 426 Ma ± 9 Ma (2s) for GZ8 are typical of unheated zircon from Sri Lanka. The mean U concentrations are 680 ?g g?¹ (GZ7) and 1305 ?g g?¹ (GZ8). The two zircon samples are proposed as reference materials for SIMS (secondary ion mass spectrometry) U-Pb geochronology. In addition, GZ7 (Ti concentration 25.08 ?g g?¹ ± 0.18 ?g g?¹; 95% confidence uncertainty) may prove useful as reference material for Ti?in?zircon temperature estimates.
Abstract: A comprehensive, internally consistent U-Pb and Lu-Hf isotope data set for 93 mantle-derived zircons from the Yakutian kimberlite province confirms and further refines the four major episodes of kimberlite magmatism on the Siberian craton: 421-409?Ma (Late Silurian-Early Devonian), 358-353?Ma (Late Devonian-Early Carboniferous), 226-218?Ma (Late Triassic), and 161-144?Ma (Middle-Late Jurassic). The relatively narrow, constant range of ?Hf values between +2 and +10 for both the Paleozoic and Mesozoic mantle-derived zircons (and by inference kimberlites) suggests that the volatile-rich magmas were repeatedly sourced from the convecting upper mantle beneath the Siberian craton. This finding is in keeping with the narrow and constant range of ?Nd values for groundmass perovskites from the Yakutian kimberlite province between +1.8 and +5.5 between 420 and 150?Ma. Our preferred model implies that the convecting upper mantle beneath the Yakutian kimberlite province ‘recovered’ rapidly back to ambient conditions shortly after the giant plume-related flood volcanic event that produced the Siberian Traps at 250?Ma. Although close spatial relationships exist between kimberlites and flood basalts on the Siberian craton during both the Paleozoic and Mesozoic, exact timing of the igneous events and the isotopic compositions of the diverse deep-sourced melting products rule out any direct genetic links. Besides the highly economic kimberlite-hosted diamond deposits of Late Devonian age (e.g., Mir and Udachnaya), the Siberian craton also contains significant Mesozoic placer diamond deposits (e.g., along the Anabar river), for which lamproite sources have been suggested recently. Our study shows that mantle-derived zircon megacryst fragments from the Ebelyakh placer deposit have Late Triassic ages of ca. 224?Ma. Their long-term depleted Hf isotopic compositions (+8.5 ?Hf) suggest that the alluvial diamonds were sourced from asthenosphere-derived Triassic kimberlites rather than from lithospheric mantle derived isotopically enriched lamproites.
Abstract: In situ U-Pb and Hf analyses were used for crustal zircon xenocrysts from Triassic kimberlites exposed in the Rangnim Massif of North Korea to identify components of the basement hidden in the deep crust of the Rangnim Massif and to clarify the crustal evolution of the massif. The U-Pb age spectrum of the zircons has a prominent population at 1.9-1.8 Ga and a lack of Archaean ages. The data indicate that the deep crust and basement beneath the Rangnim Massif are predominantly of Palaeoproterozoic age, consistent with the ages of widely exposed Palaeoproterozoic granitic rocks. In situ zircon Hf isotope data show that most of the Palaeoproterozoic zircon xenocrysts have negative ?Hf ( t ) values (?9.7 to +0.7) with an average Hf model age of 2.86 ± 0.02 Ga (2 ? ), which suggests that the Palaeoproterozoic basement was not juvenile but derived from the reworking of Archaean rocks. Considering the existence of Archaean remanent material in the Rangnim Massif and their juvenile features, a strong crustal reworking event is indicated at 1.9-1.8 Ga, during which time the pre-existing Archaean basement was exhausted and replaced by a newly formed Palaeoproterozoic basement. These features suggest that the Rangnim Massif constitutes the eastern extension of the Palaeoproterozoic Liao-Ji Belt of the North China Craton instead of the Archaean Liaonan Block as previously thought. A huge Palaeoproterozoic orogen may exist in the eastern margin of the Sino-Korean Craton.
Abstract: New in-situ U-Pb ages and Sr-Nd-Hf isotopic data on mineral phases of the Sung Valley and Jasra ultramafic-alkaline-(carbonatite) intrusions (Shillong Plateau, India) shed new light on the petrogenetic processes of volcanism in north-eastern India during the Cretaceous. Perovskites of Sung Valley dunite, ijolite and uncompahgrite yielded U-Pb ages of 109.1?±?1.6, 104.0?±?1.3 and 101.7?±?3.6?Ma, respectively. A U-Pb age of 106.8?±?1.5?Ma was obtained on zircons of a Sung Valley nepheline syenite. Perovskite of a Jasra clinopyroxenite yielded an age of 101.6?±?1.2?Ma, different from the U-Pb age of 106.8?±?0.8?Ma on zircon of Jasra syenites. The variation in Sr-Nd-Hf isotopic compositions [initial 87Sr/86Sr?=?0.70472 to 0.71080; ?Nd i?=??10.85 to +0.86; ?Hf i?=??7.43 to +1.52] matches the bulk-rock isotopic composition of the different rock units of Sung Valley and Jasra. Calcite and apatite in the carbonatites, the perovskite in a dunite, and the bulk-rock carbonatites of Sung Valley intrusion have the lowest initial 87Sr/86Sr and ?Nd, taken to be the best proxies of the mantle source composition, which is dominated by components derived from the lithospheric mantle. The alkaline intrusions of north-eastern India are significantly younger than the Sylhet tholeiitic magmatism. The silicate rocks of both intrusions have isotopic composition trending to that of the underlying Shillong crust, indicating the effects of fractional crystallization and low-pressure crustal contamination during the emplacement of the various intrusive magma pulses.
Annual Reviews of Earth and Planetary Sciences, Vol. 47, pp. 173-195.
China
craton
Abstract: The North China Craton (NCC) was originally formed by the amalgamation of the eastern and western blocks along an orogenic belt at ?1.9 Ga. After cratonization, the NCC was essentially stable until the Mesozoic, when intense felsic magmatism and related mineralization, deformation, pull-apart basins, and exhumation of the deep crust widely occurred, indicative of destruction or decratonization. Accompanying this destruction was significant removal of the cratonic keel and lithospheric transformation, whereby the thick (?200 km) and refractory Archean lithosphere mantle was replaced by a thin (<80 km) juvenile one. The decratonization of the NCC was driven by flat slab subduction, followed by a rollback of the paleo-Pacific plate during the late Mesozoic. A global synthesis indicates that cratons are mainly destroyed by oceanic subduction, although mantle plumes might also trigger lithospheric thinning through thermal erosion. Widespread crust-derived felsic magmatism and large-scale ductile deformation can be regarded as petrological and structural indicators of craton destruction.
Abstract: n situ U-Pb and Hf analyses were used for crustal zircon xenocrysts from Triassic kimberlites exposed in the Rangnim Massif of North Korea to identify components of the basement hidden in the deep crust of the Rangnim Massif and to clarify the crustal evolution of the massif. The U-Pb age spectrum of the zircons has a prominent population at 1.9-1.8 Ga and a lack of Archaean ages. The data indicate that the deep crust and basement beneath the Rangnim Massif are predominantly of Palaeoproterozoic age, consistent with the ages of widely exposed Palaeoproterozoic granitic rocks. In situ zircon Hf isotope data show that most of the Palaeoproterozoic zircon xenocrysts have negative ?Hf(t) values (?9.7 to +0.7) with an average Hf model age of 2.86 ± 0.02 Ga (2?), which suggests that the Palaeoproterozoic basement was not juvenile but derived from the reworking of Archaean rocks. Considering the existence of Archaean remanent material in the Rangnim Massif and their juvenile features, a strong crustal reworking event is indicated at 1.9-1.8 Ga, during which time the pre-existing Archaean basement was exhausted and replaced by a newly formed Palaeoproterozoic basement. These features suggest that the Rangnim Massif constitutes the eastern extension of the Palaeoproterozoic Liao-Ji Belt of the North China Craton instead of the Archaean Liaonan Block as previously thought. A huge Palaeoproterozoic orogen may exist in the eastern margin of the Sino-Korean Craton.
Geostandards and Geoanalltical Research, Vol. 43, 3, pp. 543-565.
China, Europe, Sweden, Asia, Mongolia, United States, Africa, Malawi, Madagascar
REE
Abstract: Bastnäsite is the end member of a large group of carbonate-fluoride minerals with the common formula (REE) CO3F•CaCO3. This group is generally widespread and, despite never occurring in large quantities, represents the major economic light rare earth element (LREE) mineral in deposits related to carbonatite and alkaline intrusions. Since bastnäsite is easily altered and commonly contains inclusions of earlier?crystallised minerals, in situ analysis is considered the most suitable method to measure its U?Th?Pb and Sr?Nd isotopic compositions. Electron probe microanalysis and laser ablation (multi?collector) inductively coupled plasma?mass spectrometry of forty?six bastnäsite samples from LREE deposits in China, Pakistan, Sweden, Mongolia, USA, Malawi and Madagascar indicate that this mineral typically has high Th and LREE and moderate U and Sr contents. Analysis of an in?house bastnäsite reference material (K?9) demonstrated that precise and accurate U?Th?Pb ages could be obtained after common Pb correction. Moreover, the Th?Pb age with its high precision is preferable to the U?Pb age because most bastnäsites have relatively high Th rather than U contents. These results will have significant implications for understanding the genesis of endogenous ore deposits and formation processes related to metallogenic geochronology research.
Abstract: Carbonatites are few but significant to understand carbon recycling of the earth, the crust-mantle interactions, deep mantle magmatism and regional continental evolution. The Lijiahe carbonatite intrusion, located at the Micangshan Mountains along the NW margin of the Yangtze block, South China was emplaced into the Paleoproterozoic strata, but the timing of the igneous event has long been unknown. Dating by U-Pb apatite was carried out by this work, and it gives an age of 766 ± 11 Ma (MSWD=0.15) for the carbonatitic magmatism of the region. The carbonatite comprises mainly of calcite, magnitite and apatite with minor minerals of salite, biotite, tremolite, hornblende and muscovite and accessary minerals of pyrrhotite, silver marcasite, niobite, spinel and zircon. Its spatial distribution was obviously controlled by regional tectonics. Besides, ultra-alkaline silicate intrusive complex in the region has been reported by us and other works, and mostly consists of iolite, urtite and jacupirangite with ages of ~890-875 Ma. Furthermore, a large number of gabbro and diorite plutons are found in the Micangshan Mountains and dated at ~780-760 Ma. NW margin of the Yangtze block is connected with the South Qinling orogenic belt generally thought having an affinity of the Yangtze block during the Neoproterozoic. Our works revealed that the South Qinling is discriminated from the NW Yangtze by intensive ~680 Ma igneous activities which are poorly reported in the interior of South China. Given that a ~815 Ma collision between the South Qinling ribbon and NW Yangtze margin is recognized by our recent work, the regional massive mantle-derived magmatism including the Lijiahe carbonatitic pluton is explained to indicate a drifting of South Qinling terrane from the NW margin of Yangtze block along previous weak-tectonic zones during the Rodinia breakup caused by continental rifting.
Abstract: Carbonatites are generally accepted as derived from the mantle, whereas viewpoint of carbonatitic melt formed at crust level is considered marginal. Here we document large-scale (?17?km2) igneous carbonate-rich rocks in the southeast Tarim Craton that were formed within the crust. These rocks exhibit clear intrusive contact with the wall-rocks and contain diverse xenolith, indicating an igneous origin. Zircon U-Pb dating reveals that they were emplaced at ca. 1.94-1.92 and 1.87-1.86?Ga, respectively. ?18O values in zircons (5.7-13.7‰) are higher than those crystallized in equilibrium with mantle melt. Total REE content is 1-2 magnitude lower than that of mantle carbonatite and shows weak fractionation of HREE. REE modeling reveals that the samples cannot be produced by partial melting of carbonated MORB at mantle conditions. The studied samples have positive ?13CV-PDB values (4.2-15.7‰), which are distinct from the mantle carbonatite but comparable to sedimentary carbonates. C-O-Sr-Nd isotope modelling indicates that the compositions of the studied samples cannot be produced by evolution of mantle carbonatite. Integrating these lines of evidence, we conclude that the studied carbonate-rich magmatic rocks were derived from partial melting of impure marble at crustal level via fluid-present melting. These carbonatites probably represent the initial magmatic record of tectonic extension of the late Paleoproterozoic collisional orogenic belt in the southern margin of the Tarim craton. The positive carbon excursion recorded by the high ?13CV-PDB values probably corresponds to the global Paleoproterozoic Lomagundi-Jatuli event. Our study implies that partial melting of sedimentary carbonates is more common than previously thought, which has significant impacts on crust rheology and global carbon cycling
Journal of Geophysical Research: Planets, doei:10.1029/ 2018JE005698
Mantle
water
Abstract: People have long had curiosity in the origin of Earth's water (equivalently hydrogen). Solar nebula has been given the least attention among existing theories, although it was the predominating reservoir of hydrogen in our early solar system. Here we present a first model for Earth's water origin that quantifies contribution from the solar nebula in addition to that from chondrites, the primary building blocks of Earth. The model considers dissolution of nebular hydrogen into the early Earth's magma oceans and reaction between hydrogen and iron droplets within the magma ocean. Such processes not only delivered countless hydrogen atoms from the mantle to the core but also generated an appreciable difference in hydrogen isotopic composition (2H/1H ratio) between the mantle and core. Fitting the model to current knowledge about Earth's hydrogen produces best combinations of nebular and chondritic contributions to Earth's water. We find that nearly one out of every 100 water molecules on Earth came from the solar nebula. Our planet hides majority of its water inside, with roughly two oceans in the mantle and four to five oceans in the core. These results suggest inevitable formation of water on sufficiently large rocky planets in extrasolar systems.
Abstract: From Columbia to Rodinia to Pangaea, Earth has seen a few supercontinents come and go in its ancient past. Now, researchers theorize that these giant landmasses form in regular cycles, about once every 600 million years. They even predict when and where the next supercontinent will form, driven by the creeping flow of rocks in our planet’s hot mantle.
Geological Society of America Bulletin, Vol. 133, pp. 1128-1140.
United States
tectonics
Abstract: The configuration of mid-ocean ridges subducted below North America prior to Oligocene time is unconstrained by seafloor isochrons and has been primarily inferred from upper-plate geology, including near-trench magmatism. However, many tectonic models are permitted from these constraints. We present a fully kinematic, plate tectonic reconstruction of the NW Cordillera since 60 Ma built by structurally unfolding subducted slabs, imaged by mantle tomography, back to Earth’s surface. We map in three-dimensions the attached Alaska and Cascadia slabs, and a detached slab below western Yukon (Canada) at 400-600 km depth that we call the “Yukon Slab.” Our restoration of these lower plates within a global plate model indicates the Alaska slab accounts for Pacific-Kula subduction since ca. 60 Ma below the Aleutian Islands whereas the Cascadia slab accounts for Farallon subduction since at least ca. 75 Ma below southern California, USA. However, intermediate areas show two reconstruction gaps that persist until 40 Ma. We show that these reconstruction gaps correlate spatiotemporally to published NW Cordillera near-trench magmatism, even considering possible terrane translation. We attribute these gaps to thermal erosion related to ridge subduction and model mid-ocean ridges within these reconstruction gap mid-points. Our reconstructions show two coeval ridge-trench intersections that bound an additional “Resurrection”-like plate along the NW Cordillera prior to 40 Ma. In this model, the Yukon slab represents a thermally eroded remnant of the Resurrection plate. Our reconstructions support a “northern option” Farallon ridge geometry and allow up to ?1200 km Chugach terrane translation since Paleocene time, providing a new “tomographic piercing point” for the Baja-British Columbia debate.
Abstract: The Late Cretaceous kimberlites in northern Alberta, Canada, intruded into the Paleoproterozoic crust and represent a nonconventional setting for the discovery of diamonds. Here, we examined the origin of kimberlite magmatism using a multidisciplinary approach. A new teleseismic survey reveals a low-velocity (-1%) corridor that connects two deep-rooted (>200 km) quasi-cylindrical anomalies underneath the Birch Mountains and Mountain Lake kimberlite fields. The radiometric data, including a new U-Pb perovskite age of 90.3 ± 2.6 Ma for the Mountain Lake intrusion, indicate a northeast-trending age progression in kimberlite magmatism, consistent with the (local) plate motion rate of North America constrained by global plate reconstructions. Taken together, these observations favor a deep stationary (relative to the lower mantle) source region for kimberlitic melt generation. Two competing models, mantle plume and slab subduction, can satisfy kinematic constraints and explain the exhumation of ultradeep diamonds. The plume hypothesis is less favorable due to the apparent age discrepancy between the oldest kimberlites (ca. 90 Ma) and the plume event (ca. 110 Ma). Alternatively, magma generation may have been facilitated by decompression of hydrous phases (e.g., wadsleyite and ringwoodite) within the mantle transition zone in response to thermal perturbations by a cold slab. The three-dimensional lithospheric structures largely controlled melt migration and intrusion processes during the Late Cretaceous kimberlite magmatism in northern Alberta.
Geological Society of America Bulletin, Vol. 133, 3/4, pp. 625-646. pdf
Global
Pangea
Abstract: The supercontinent Pangea formed by the subduction of the Iapetus and Rheic oceans between Gondwana, Laurentia, and Baltica during mid-to-late Paleozoic times. However, there remains much debate regarding how this amalgamation was achieved. Most paleogeographic models based on paleomagnetic data argue that the juxtaposition of Gondwana and Laurussia (Laurentia-Baltica) was achieved via long-lasting highly oblique convergence in the late Paleozoic. In contrast, many geology-based reconstructions suggest that the collision between the two continents was likely initiated via a Gondwanan promontory comprising the Iberian, Armorican, and Bohemian massifs, and parts of the basement units in the Alpine orogen during the Early Devonian. To help resolve this discrepancy, we present an updated compilation of high-quality paleopoles of mid-to-late Paleozoic ages (spanning Middle Ordovician and Carboniferous times) from Gondwana, Laurentia, and Baltica. These paleopoles were evaluated with the Van der Voo selection criteria, corrected for inclination error where necessary, and were used to revise their apparent polar wander (APW) paths. The revised APW paths were constructed using an innovative approach in which age errors, A95 ovals, and Q-factors of individual paleopoles are taken into account. By combining the resulting APW paths with existing geological data and field relationships in the European Variscides, we provide mid-to-late Paleozoic paleogeographic reconstructions which indicate that the formation of Pangea was likely initiated at 400 Ma via the collision between Laurussia and a ribbon-like Gondwanan promontory that was itself formed by a scissor-like opening of the Paleotethys Ocean, and that the amalgamation culminated in the mostly orthogonal convergence between Gondwana and Laurussia.
Abstract: Knowledge about the viscosity and other transport properties of CaCO3 melts at high pressures and temperatures relevant to the Earth’s mantle is critically important for understanding the deep carbon cycle [1,2]. We have conducted First-Principles Molecular Dynamics Calculations of CaCO3 melts up to 52.5 GPa and 3000 K to provide atomistic insights into the mechanisms of diffusion and viscosity. Our calculated viscosities of CaCO3 melts at low pressures are in good agreement with those from experiments. In particular, viscosity is almost constant at low pressures but increases linearly with pressure above 10 GPa. The ultralow viscosity of CaCO3 melts at low pressures [1] is readily attributed to the uncorrelated diffusion of Ca2+ and CO3 2- ions (Fig. 1). In contrast, the motions of the Ca2+ cations and CO3 2- anions at pressures >10 GPa become increasingly correlated (Fig. 1), leading to higher viscosities. Compared to water, the viscosity of CaCO3 melts is not anomalously low. Rather, the viscosity of water is anomalously high, because water molecules are strongly H-bonded and behave like polymers.
Abstract: Although REE (lanthanides + Sc + Y) mineralization in alkaline silicate systems is commonly accompanied with Zr mineralization worldwide, our understanding of the relationship between Zr and REE mineralization is still incomplete. The Baerzhe deposit in Northeastern China is a reservoir of REE, Nb, Zr, and Be linked to the formation of an Early Cretaceous, silica-saturated, alkaline intrusive complex. In this study, we use in situ laser ablation-inductively coupled plasma-mass spectrometry (LA-ICP-MS) analyses of zircon and monazite crystals to constrain the relationship between Zr and REE mineralization at Baerzhe. Three groups of zircon are identified and are differentiated based upon textural observations and compositional characteristics. Type Ia zircons display well-developed oscillatory zoning. Type Ib zircons are darker in cathodoluminescence images and have more irregular zoning and resorption features than type Ia zircons. In addition, type Ib zircons can locally occur as overgrowths on type Ia zircons. Type II zircons contain irregular but translucent cores and rims with oscillatory zoning that are murky brown in color and occur in aggregates. Textural features and compositional data suggest that types Ia and Ib zircon crystallized at the magmatic stage, with type Ia being least-altered and type Ib being strongly altered. Type II zircons, on the other hand, precipitated during the magmatic to magmatichydrothermal transition. Whereas the magnitude of the Eu anomaly is moderate in the barren alkaline granite, both magmatic and deuteric zircon exhibit pronounced negative anomalies. Such features are difficult to explain exclusively by feldspar fractionation and could indicate the presence of fluid induced modification of the rocks. Monazite crystals occur mostly through replacement of zircon and sodic amphibole; monazite clusters are also present. Textural and compositional evidence suggests that monazite at Baerzhe is hydrothermal. Types Ia and Ib magmatic zircon yield 207Pb-corrected 206Pb/238U ages of 127.2 ± 1.3 and 125.4 ± 0.7 Ma, respectively. Type II deuteric zircon precipitated at 124.9 ± 0.6 Ma. The chronological data suggest that the magmatic stage of the highly evolved Baerzhe alkaline granite lasted less than two million years. Hydrothermal monazite records a REE mineralization event at 122.8 ± 0.6 Ma, approximately 1 or 2 million years after Zr mineralization. We therefore propose a model in which parental magmas of the Baerzhe pluton underwent extensive magmatic differentiation while residual melts interacted with aqueous hydrothermal fluids. Deuteric zircon precipitated from a hydrosilicate liquid, and subsequent REE mineralization, exemplified by hydrothermal monazite, correlates with hydrothermal metasomatic alteration that postdated the hydrosilicate liquid event. Such interplay between magmatic and hydrothermal processes resulted in the formation of discrete Zr and REE mineralization at Baerzhe.
Mineralogy and Petrology, in press available, 14p.
Africa, South Africa
deposit - Bultfontein
Abstract: MARID (Mica-Amphibole-Rutile-Ilmenite-Diopside) and PIC (Phlogopite-Ilmenite-Clinopyroxene) xenoliths are thought to be formed by intense Bprimary^ mantle metasomatism. These rocks also display secondary features, such as cross-cutting veins and geochemical zonation of matrix minerals, which probably reflect latermetasomatic events. To investigate the nature and origin(s) of these secondary features, 28 MARID and PIC xenoliths from southern African kimberlites and orangeites have been studied. MARID-hosted veins contain both carbonate and Ti-rich phases (e.g., titanite, phlogopite), suggesting that they formed by the infiltration of a carbonated silicate melt. Elevated TiO2 contents in MARID matrix mineral rims are spatially associated with carbonate-dominated veins, suggesting a genetic relationship between vein formation and geochemical zonation. Spongy rims around primaryMARID and PIC clinopyroxene are depleted in Na2O andAl2O3 relative to their cores, possibly reflecting mineral dissolution in the xenoliths during ascent and emplacement of the entraining kimberlite. The preservation of compositional differences between primary and secondary phases in MARID and PIC xenoliths indicates that metasomatism occurred shortly before, or broadly coeval with, kimberlite/orangeite magmatism; otherwise, at typical mantle temperatures, such features would have quickly re-equilibrated. Increased Na2O in some mineral rims (e.g., K-richterite) may therefore reflect equilibration with a more Na-enriched primitive kimberlite melt composition than is commonly suggested. Vein-hosted clinopyroxene 87Sr/86Sri (0.70539 ± 0.00079) in one MARID sample is intermediate between primary clinopyroxene in the sample (0.70814 ± 0.00002) and the host Bultfontein kimberlite (0.70432 ± 0.00005), suggesting that vein minerals are derived from interactions between primary MARID phases and kimberlite-related melts/fluids. Sulfur isotope compositions of barite (?34SVCDT = +4.69 ‰) and sulfides (?34SVCDT = ?0.69 ‰) in carbonate veins reflect equilibration at temperatures of 850-900 °C, consistent with sulfurrich melt/fluid infiltration in the lithospheric mantle. In contrast, vein carbonate C-O isotope systematics (?13CVPDB = ?9.18 ‰ ?18OVSMOW = +17.22‰) are not typical of kimberlites or other mantle carbonates (?13CVPDB = ?3 to ?8‰ ?18OVSMOW = 6 to 9 ), and may represent post-emplacement hydrothermal interactions of the cooling kimberlite with crustal fluids. These constraints suggest protracted metasomatism of MARID rocks shortly before and during entrainment by the host kimberlite.
Abstract: Baddeleyite is a frequently found accessory mineral in silica undersaturated lavas. Because it is typically enriched in uranium, while having low initial lead, baddeleyite has long been a prime target for U-Pb geochronology of mafic rocks. The difficulties in retrieving small baddeleyite grains from volcanic samples and the lack of a detailed understanding of baddeleyite occurrence, however, have limited baddeleyite chronology largely to coarse-grained mafic intrusive rocks. Here, the development of U-Th in situ baddeleyite analysis using secondary ionization mass spectrometry (SIMS) is presented together with an assessment of baddeleyite occurrence in Quaternary silica-undersaturated lavas from Campi Flegrei (Naples, Italy). Samples studied comprise the pre- and post Campanian Ignimbrite (ca. 40 ka) lava domes of Cuma and Punta Marmolite, and Astroni and Accademia, respectively. The in situ sample preparation required initial identification of baddeleyite crystals from sawed and polished rock billets using scanning electron microscope (SEM) backscatter imaging and energy-dispersive X-ray analysis. U-Th baddeleyite isochron ages for intra-caldera Astroni and Accademia lava domes are 5.01+2.61?2.55 ka (MSWD = 2.0; n = 17) and 4.36+1.13?1.12 ka (MSWD = 2.9; n = 24), respectively. The ages for Punta Marmolite (62.4+3.9?3.8 ka; MSWD = 1.2; n = 11) and Cuma (45.9+3.6?3.5 ka; MSWD = 2.2; n = 11) predate the Campanian Ignimbrite. Rapid baddeleyite crystallization at the time of emplacement is supported by petrologic observations that >50% of the baddeleyite crystals documented in this study occur either in vesicles or in vesicle-rich regions of the host lavas whose textures developed over timescales of a few years to a few decades based on microlite crystal size distribution (CSD) analysis. Radiometric U-Th baddeleyite ages are mostly in agreement with previously determined K-Ar eruption ages, except for the Punta Marmolite lava dome whose U-Th baddeleyite age predates the K-Ar age by ca. 15 ka. Baddeleyite thus records eruptive emplacement with little evidence for significant pre-eruptive crystal residence, and has potential as an eruption chronometer for Quaternary silica-undersaturated volcanic rocks.
Geological Society of America Annual Meeting, Vol. 47, 7, p. 163. abstract
Europe, Turkey
Moissanite
Abstract: The Aladag ophiolite in the eastern Tauride belt, southern Turkey, is a well-preserved remnant of oceanic lithosphere. It consists of, in ascending order, harzburgitic to dunitic tectonites, ultramafic and mafic cumulates, isotropic gabbros, sheeted dikes and basaltic pillow lavas. Podiform chromitites are common in the mantle peridotites. Thus far, more than 200 grains of microdiamond and more than 100 grains of moissanite (SiC) have been separated from one sample of podiform chromitite. The microdiamonds occur mostly as subhedral to euhedral, colorless to pale yellow grains, about 50-300 ?m in size. Moissanite grains are generally subhedral, light blue to deep blue in color and variable in size. These grains of diamond and moissanite are very similar to in-situ grains in podiform chromitites of Tibet and the Polar Urals of Russia (Yang et al., 2014; 2015), indicating that they are natural minerals, not the result of natural or anthropogenic contamination. As reported elsewhere, the diamonds and moissanite are accompanied by a range of other minerals, including rutile, zircon, quartz and sulfides. The discovery of diamond, moissanite and other unusual minerals in the podiform chromitites of the Aladag massif provide additional evidence for the widespread occurrence of these minerals in ophiolites, indicating that they are related to global mantle processes.
Abstract: The Pozanti-Karsanti ophiolite situated in the eastern Tauride belt, southern Turkey, is a well-preserved oceanic lithosphere remnant comprising, in ascending order, mantle peridotite, ultramafic and mafic cumulates, isotropic gabbros, sheeted dikes, and basaltic pillow lavas. Two types of chromitites are observed in the Pozanti-Karsanti ophiolite. One type of chromitites occurs in the cumulate dunites around the Moho, and the other type of chromitites is hosted by the mantle harzburgites below the Moho. The second type of chromitites has massive, nodular, and disseminated textures. We have conducted the mineral separation work on the podiform chromitites hosted by harzburgites. So far, more than 100 grains of microdiamond and moissanite (SiC) have been recovered from the podiform chromitite. The diamonds and moissanite are accompanied by large amounts of rutile. Besides zircon, monazite and sulfide are also very common phases within the separated minerals. The discovery of diamond, moissanite, and the other unusual minerals from podiform chromitite of the Pozanti-Karsanti ophiolite provides new evidences for the common occurrences of these unusual minerals in ophiolitic peridotites and chromitites. This discovery also suggests that deep mantle processes and materials have been involved in the formation of podiform chromitite.
Abstract: In recent years diamonds and other unusual minerals (carbides, nitrides, metal alloys and native elements) have been recovered from mantle peridotites and chromitites (both high-Cr chromitites and high-Al chromitites) from a number of ophiolites of different ages and tectonic settings. Here we report a similar assemblage of minerals from the Skenderbeu massif of the Mirdita zone ophiolite, west Albania. So far, more than 20 grains of microdiamonds and 30 grains of moissanites (SiC) have been separated from the podiform chromitite. The diamonds are mostly light yellow, transparent, euhedral crystals, 200-300 ?m across, with a range of morphologies; some are octahedral and cuboctahedron and others are elongate and irregular. Secondary electron images show that some grains have well-developed striations. All the diamond grains have been analyzed and yielded typical Raman spectra with a shift at ?1325 cm?1. The moissanite grains recovered from the Skenderbeu chromitites are mainly light blue to dark blue, but some are yellow to light yellow. All the analyzed grains have typical Raman spectra with shifts at 766 cm?1, 787 cm?1, and 967 cm?1. The energy spectrums of the moissanites confirm that the grains are composed entirely of silicon and carbon. This investigation expands the occurrence of diamonds and moissanites to Mesozoic ophiolites in the Neo-Tethys. Our new findings suggest that diamonds and moissanites are present, and probably ubiquitous in the oceanic mantle and can provide new perspectives and avenues for research on the origin of ophiolites and podiform chromitites.
Contributions to Mineralogy and Petrology, doi.org:10.1007/ s00410-018-1499-5 19p.
Europe, Turkey
diamond inclusions
Abstract: The Pozanti-Karsanti ophiolite (PKO) is one of the largest oceanic remnants in the Tauride belt, Turkey. Micro-diamonds were recovered from the podiform chromitites, and these diamonds were investigated based on morphology, color, cathodoluminescence, nitrogen content, carbon and nitrogen isotopes, internal structure and inclusions. The diamonds recovered from the PKO are mainly mixed-habit diamonds with sectors of different brightness under the cathodoluminescence images. The total ?13C range of the PKO diamonds varies between ? 18.8 and ? 28.4‰, with a principle ?13C mode at ? 25‰. Nitrogen contents of the diamonds range from 7 to 541 ppm with a mean value of 171 ppm, and the ?15N values range from ? 19.1 to 16.6‰, with a ?15N mode of ? 9‰. Stacking faults and partial dislocations are commonly observed in the Transmission Electron Microscopy foils whereas inclusions are rather rare. Combinations of ( Ca0.81Mn0.19)SiO3, NiMnCo-alloy and nanosized, quenched fluid phases were observed as inclusions in the PKO diamonds. We believe that the 13C-depleted carbon signature of the PKO diamonds derived from previously subducted crustal matter. These diamonds may have crystallized from C-saturated fluids in the asthenospheric mantle at depth below 250 km which were subsequently carried rapidly upward by asthenospheric melts.
Abstract: Geophysical investigations and laboratory experiments provide strong evidence for subduction of ancient oceanic crust, and geological and mineralogical observations suggest that subducted oceanic crust is recycled into the upper mantle. This model is supported by some direct petrologic and miner-alogical evidence, principally the recovery of super-deep diamonds from kimberlites and the presence of crustal materials in ophiolitic chromitites and peridotites, but many details are still unclear. Here we report the discovery of ophiolite-hosted diamonds in the podiform chromitites of the Skenderbeu massif of the Mirdita ophiolite in the western part of Neo-Tethys. The diamonds are characterized by exceedingly light C isotopes (?13CPDB ~ -25‰), which we interpret as evidence for subduction of organic carbon from Earth's surface. They are also characterized by an exceptionally large range in ? 15Nair (-12.9‰ to +25.5‰), accompanied by a low N aggregation state. Materials sparsely included in diamonds include amorphous material, Ni-Mn-Co alloy, nanocrystals (20 × 20 nm) of calcium silicate with an orthorhombic perovskite structure (Ca-Pv), and fluids. The fluids coexisting with the alloy and Ca-Pv provide clear evidence that the diamonds are natural rather than synthetic. We suggest that the Skenderbeu diamonds nucleated and grew from a C-saturated, NiMnCo-rich melt derived from a subducted slab of ocean crust and lithosphere in the deep mantle, at least in the diamond stability field, perhaps near the top of the mantle transition zone. The subsequent rapid upward transport in channeled networks related to slab rollback during subduction initiation may explain the formation and preservation of Skenderbeu diamonds. The discovery of diamonds from the Mirdita ophiolite not only provides new evidence of diamonds in these settings but also provides a valuable opportunity to understand deep cycling of subducted oceanic crust and mantle composition.
Abstract: The North China Craton (NCC) is an atypical ancient landmass that suffered lithospheric destruction. Previous studies suggest that the eastern part of the lithospheric mantle of the NCC has been thinned and modified in the Mesozoic. However, the initiation time and mechanism of the destruction remain controversial. Mafic magmatismcould provide a unique windowinto deciphering the lithospheric mantle composition and its evolution. Here we present geochemical and geochronological data of the diamond-bearing alkaline basalts from Lan'gan, located in the southeastern margin of the NCC. Zircon U-Pb dating yielded an average age of 174 ± 14 Ma, representing the first reported Jurassic basalts in the eastern NCC. The Lan'gan basalts are enriched in light rare earth elements (LREE) and large ion lithosphile elements (LILE). Sr-Nd-Pb-Hf isotopic compositions (87Sr/86Sr(t) = 0.70646-0.70925, ?Nd(t) = ?2.1 to ?4.9, 206Pb/204Pb(t) = 17.14-18.12, 207Pb/204Pb(t) = 15.28-15.61, 208Pb/204Pb(t) = 37.82-38.67, and zircon ?Hf(t) = ?17 to ?21) are enriched compared to depleted mantle. The presence of primary amphibole indicates that the magma source of the basalts was water enriched. These observations suggest that, the lithospheric mantle of the eastern NCC were significantly refertilized, likely by slab derived fluids/melts fromthe Paleo-Pacific subduction. Owing to the Paleo-Pacific subduction, the lithosphericmantle of the eastern NCCwere reduced in viscosity and intensity, and finally promoted partialmelting in a limited scale to generate the investigated alkaline basalts. Hence, the discovery of diamond in the Lan'gan basalts demonstrates that the lithosphere of the NCC remained thick, and that large-scale destruction had not initiated in the early Jurassic beneath this region.
Abstract: Precise measurement of variations in the local gravitational acceleration is valuable for natural hazard forecasting, prospecting, and geophysical studies. Common issues of the present gravimetry technologies include their high cost, high mass, and large volume, which can potentially be solved by micro-electromechanical-system (MEMS) technology. However, the reported MEMS gravimeter does not have a high sensitivity and a large dynamic range comparable with those of the present commercial gravimeters, lowering its practicability and ruling out worldwide deployment. In this paper, we introduce a more practical MEMS gravimeter that has a higher sensitivity of 8??Gal/?Hz and a larger dynamic range of 8000 mGal by using an advanced suspension design and a customized optical displacement transducer. The proposed MEMS gravimeter has performed the co-site earth tides measurement with a commercial superconducting gravimeter GWR iGrav with the results showing a correlation coefficient of 0.91.
Abstract: The North China Craton (NCC) is an atypical ancient landmass that suffered lithospheric destruction. Previous studies suggest that the eastern part of the lithospheric mantle of the NCC has been thinned and refertilized in the Mesozoic. However, the initiation time and mechanism of the destruction remain controversial. Mafic magmatism could provide a unique window into deciphering the lithospheric mantle composition and its evolution. Here we present geochemical and geochronological data of the diamond-bearing alkaline basalts from Lan'gan, located in the southeastern margin of the NCC. Zircon UPb dating yielded an average age of 174?±?14?Ma, representing the first reported Jurassic basalts in the eastern NCC. The Lan'gan basalts are enriched in light rare earth elements (LREE) and large ion lithosphile elements (LILE). Sr-Nd-Pb-Hf isotopic compositions (87Sr/86Sr(t)?=?0.70646-0.70925, ?Nd(t)?=??2.1 to ?4.9, 206Pb/204Pb(t)?=?17.14-18.12, 207Pb/204Pb(t)?=?15.28-15.61, 208Pb/204Pb(t)?=?37.82-38.67, and zircon ?Hf(t)?=??17 to ?21) are slightly enriched compared to depleted mantle. The presence of primary amphibole indicates that the magma source of the basalts was water enriched. These observations suggest that, the lithospheric mantle of the eastern NCC were significantly refertilized, likely by slab derived fluids/melts from the Paleo-Pacific subduction. Owing to the Paleo-Pacific subduction, the lithospheric mantle of the eastern NCC were reduced in viscosity and intensity, and finally promoted partial melting in a limited scale to generate the investigated alkaline basalts. Hence, the discovery of diamond in the Lan'gan basalts demonstrates that the lithosphere of the NCC remained thick, and that large-scale destruction had not initiated in the early Jurassic beneath this region.
Abstract: Geophysical investigations and laboratory experiments show evidence for possible subduction of ancient oceanic crust. Geological and mineralogical observations suggest that subducted oceanic crust is recycled into the upper mantle. The subduction is supported by the recovery of super?deep diamonds from kimberlites and the presence of crustal materials in ophiolitic chromitites and their host peridotites. What is the mechanism? Here we report the new discovery of ophiolite?hosted diamonds in the podiform chromitites within the Skenderbeu massif from the Mirdita ophiolite in the western part of Neo?Tethys (Fig. 1). The diamonds are characterized by exceedingly light C isotopes (?13CPDB ? ?25‰), which can be interpreted as evidence for subduction of organic carbon from Earth's surface. The diamonds are also characterized by an exceptionally large range in ?15Nair (?12.9‰ to +25.5‰), accompanied by a low N aggregation state (Fig. 2). On the other hand, materials sparsely included in diamonds include amorphous material, Ni?Mn?Co alloy, nanocrystals (20 nm×20 nm) of calcium silicate with an orthorhombic perovskite structure (Ca?Pv), and fluids (Fig. 3). We consider that the Skenderbeu diamonds nucleated and grew from a C?saturated, NiMnCo?rich melt derived from a subducted slab of ocean crust and lithosphere in the deep mantle environment. The environment is in the diamond stability field or near the top of the mantle transition zone. The new discovery of diamonds from the Mirdita ophiolite provides a valuable opportunity to understand deep cycling of subducted oceanic crust and mantle (i.e., composition and process).
Abstract: Farré?de?Pablo et al. (2018) report a new occurrence of in situ microdiamonds enclosed in chromite from ophiolitic chromitite pods hosted in the Tehuitzingo serpentinite of southern Mexico. The discovery enlarges the number of occurrence of the ophiolite?hosted microdiamonds to 7 countries in the world, including India (Das, 2015, 2017), Albania (Xiong et al., 2017; Wu et al., 2017), Turkey (Lian et al., 2017), Myanmar (Chen et al., 2018), Russia (Yang et al., 2015), and China (Bai et al., 1993; Xu et al., 2009). The microdiamonds occur in ophiolitic podiform chromitites and peridotites, and are generally interpreted as UHP phases formed at pressures > 4 GPa (Yang et al., 2014; Griffin et al., 2016; Das et al., 2017). However, Farré?de?Pablo et al. (2018) conclude that the Tehuitzingo diamonds were formed under low?temperature and low?pressure conditions during serpentinization, which challenges the current knowledge of diamond formation. Here, we discuss several lines of evidence that do not support the authors' conclusion.
Science China Earth Sciences, Vol. 60, 2, pp. 207-217.
Technology
Subduction
Abstract: Diamonds are renowned as the record of Earth’s evolution history. Natural diamonds on the Earth can be distinguished in light of genetic types as kimberlitic diamonds (including peridotitic diamonds and eclogitic diamonds), ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds. According to the inclusion mineralogy, most diamonds originated from continental lithospheric mantle at depths of 140-250 km. Several localities, however, yield ultradeep diamonds with inclusion compositions that require a sublithospheric origin (>~250 km). Ultradeep diamonds exhibit distinctions in terms of carbon isotope composition, N-concentration, mineral inclusions and so on. The present study provides a systematic compilation concerning the features of ultradeep diamonds, based on which to expound their genesis affinity with mantle-carbonate melts. The diamond-parental carbonate melts are proposed to be stemmed from the Earth’s crust through subduction of oceanic lithosphere. Ultradeep diamonds are classified into a subgroup attaching to kimberlitic diamonds grounded by formation mechanism, and present connections in respect of carbon origin to eclogitic diamonds, ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds.
Abstract: Diamonds are renowned as the record of Earth’s evolution history. Natural diamonds on the Earth can be distinguished in light of genetic types as kimberlitic diamonds (including peridotitic diamonds and eclogitic diamonds), ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds. According to the inclusion mineralogy, most diamonds originated from continental lithospheric mantle at depths of 140-250 km. Several localities, however, yield ultradeep diamonds with inclusion compositions that require a sublithospheric origin (>~250 km). Ultradeep diamonds exhibit distinctions in terms of carbon isotope composition, N-concentration, mineral inclusions and so on. The present study provides a systematic compilation concerning the features of ultradeep diamonds, based on which to expound their genesis affinity with mantle-carbonate melts. The diamond-parental carbonate melts are proposed to be stemmed from the Earth’s crust through subduction of oceanic lithosphere. Ultradeep diamonds are classified into a subgroup attaching to kimberlitic diamonds grounded by formation mechanism, and present connections in respect of carbon origin to eclogitic diamonds, ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds.
Abstract: Diamonds are renowned as the record of Earth’s evolution history. Natural diamonds on the Earth can be distinguished in light of genetic types as kimberlitic diamonds (including peridotitic diamonds and eclogitic diamonds), ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds. According to the inclusion mineralogy, most diamonds originated from continental lithospheric mantle at depths of 140–250 km. Several localities, however, yield ultradeep diamonds with inclusion compositions that require a sublithospheric origin (>~250 km). Ultradeep diamonds exhibit distinctions in terms of carbon isotope composition, N-concentration, mineral inclusions and so on. The present study provides a systematic compilation concerning the features of ultradeep diamonds, based on which to expound their genesis affinity with mantle-carbonate melts. The diamond-parental carbonate melts are proposed to be stemmed from the Earth’s crust through subduction of oceanic lithosphere. Ultradeep diamonds are classified into a subgroup attaching to kimberlitic diamonds grounded by formation mechanism, and present connections in respect of carbon origin to eclogitic diamonds, ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds.
Guo, S., Ye, K., Wu, Y., Chen, Y., Yang, Y., Zhang, L., Liu, J., Mao, Q., Ma, Y.
A potential method to confirm the previous existence of lawsonite in eclogite: the mass imbalance of Sr and LREEs in multi stage epidote ( Ganghe, Dabie UHP terrane).
Journal of Metamorphic Gology, Vol. 31, 4, pp. 415-435.
Geochimica et Cosmochimica Acta, Vol. 186, pp. 207-225.
Mantle
Subduction, melting
Abstract: The subducted continental crust material will be gravitationally trapped in the deep mantle after having been transported to depths of greater than ?250 -300 km (the “depth of no return”). However, little is known about the status of this trapped continental material as well as its contribution to the mantle heterogeneity after achieving thermal equilibrium with the surrounding mantle. Here, we conduct an experimental study over pressure and temperature ranges of 9 -16 GPa and 1300 -1800 °C to constrain the fate of these trapped upper continental crust (UCC). The experimental results show that partial melting will occur in the subducted UCC along normal mantle geotherm to produce K-rich melt. The residual phases composed of coesite/stishovite + clinopyroxene + kyanite in the upper mantle, and stishovite + clinopyroxene + K-hollandite + garnet + CAS-phase in the mantle transition zone (MTZ), respectively. The residual phases achieve densities greater than the surrounding mantle, which provides a driving force for descent across the 410-km seismic discontinuity into the MTZ. However, this density relationship is reversed at the base of the MTZ, leaving the descended residues to be accumulated above the 660-km seismic discontinuity and may contribute to the “second continent”. The melt is ?0.6 -0.7 g/cm3 less dense than the surrounding mantle, which provides a buoyancy force for ascent of melt to shallow depths. The ascending melt, which preserves a significant portion of the bulk-rock rare earth elements (REEs), large ion lithophile elements (LILEs), and high-filed strength elements (HFSEs), may react with the surrounding mantle. Re-melting of the metasomatized mantle may contribute to the origin of the “enriched mantle sources” (EM-sources). Therefore, the deep subducted continental crust may create geochemical/geophysical heterogeneity in Earth’s interior through subduction, stagnation, partial melting and melt segregation.
Abstract: Intergranular coesite is extremely rare in, and bears crucial information on the formation and preservation of, ultrahigh-pressure (UHP) rocks. Here, we report the first occurrence of intergranular coesite in a metasedimentary rock, which occurs in the Ganjialing area in the Dabie Shan, east-central China, and contains abundant coesite inclusions in both garnet and dolomite. We investigated the content of structural water in these minerals with Fourier transform infrared spectroscopy. Our new results undermine the ubiquity of the “pressure-vessel” model and highlight the role of reaction kinetics in preserving coesite due to the availability of water in UHP rocks.
Isotopic constraints on age and duration of fluid assisted high pressure eclogite facies recrystallization during exhumation of deeply subducted continental crurs
Journal of Metamorphic Geology, Vol. 24, 8, pp. 687-702.
Melting of subducted continent: element and isotopic evidence for a genetic relationship between Neoproterozoic and Mesozoic granitoids in the Sulu orogen.
Chemical Geology, Vol. 229, 4, May 30, pp. 227-256.
Two episodes of zircon growth due to fluid availablility during subduction and exhumation of continental crust: U Pb age, Hf and O isotope evidence from ultrahigh pressure eclogite
Frontiers in Mineral Sciences 2007, Joint Meeting of Mineralogical societies Held June 26-28, Cambridge, Abstract Volume p. 259-260.
Two episodes of zircon growth due to fluid availablility during subduction and exhumation of continental crust: U Pb age, Hf and O isotope evidence from ultrahigh pressure eclogite
Frontiers in Mineral Sciences 2007, Joint Meeting of Mineralogical societies Held June 26-28, Cambridge, Abstract Volume p. 259-260.
Deep subduction of continental crust in accretionary orogen: evidence from U-Pb dating on diamond-bearing zircons from the Qinling orogen, central China.
Earth and Planetary Science Letters, Vol. 496, pp. 80-88.
Mantle
perovskite, hotspots
Abstract: Mineralogical studies indicate that two major phase transitions occur near the depth of 660 km in the Earth's pyrolitic mantle: the ringwoodite (Rw) to perovskite (Pv) + magnesiowüstite (Mw) and the majorite (Mj) to perovskite (Pv) phase transitions. Seismological results also show a complicated phase boundary structure at this depth in plume regions. However, previous geodynamical modeling has mainly focused on the effects of the Rw-Pv+Mw phase transition on plume dynamics and has largely neglected the effects of the Mj-Pv phase transition. Here, we develop a 3-D regional spherical geodynamic model to study the combined influence of these two phase transitions on plume dynamics. Our results show the following: (1) A double phase boundary occurs in the high-temperature center of the plume, corresponding to the double reflections in seismic observations. Other plume regions feature a single, flat uplifted phase boundary, causing a gap of high seismic velocity anomalies. (2) Large amounts of relatively low-temperature plume materials can be trapped in the transition zone due to the combined effects of phase transitions, forming a complex truncated cone shape. (3) The Mj-Pv phase transition greatly enhances the plume penetration capability through 660-km phase boundary, which has a significant influence on the plume dynamics. Our results provide new insights which can be used to better constrain the 660-km discontinuity variations, seismic wave velocity structure and plume dynamics in the mantle transition zone. The model can also help to estimate the mantle temperature and Clapeyron slopes at the 660 km phase boundary.
Africa, South Africa, China, United States, Canada, South America
diamond inclusions
Abstract: We present the first evidence for inclusions of ice-VII in diamonds from southern Africa, China, North- and South-America [1]. Combining synchrotron X-ray diffraction, - X-ray fluorescence and IR spectroscopy, we show the presence of ice-VII as inclusions in diamonds that have formed at depth > 410 km to about 800 km in the Earth's mantle. What is now crystalline ice-VII, a high pressure polymorph of water-ice, was component of an aqueous fluid entrapped in the diamonds that were growing in the deep mantle. Because of the confinement by the host diamonds, the inclusions retain high pressures. The same holds for inclusions of magnesian calcite, halite, and ilmenite found in the same diamond specimens. These inclusions reflect the presence of aqueous and carbonaceous fluids in the mantle transition zone and the shallow lower mantle. Using their current residual pressures and the equations of state, we can reconstruct their recovery paths [2,3]. Further, we can use the intersection of modelled recovery paths to better constrain the encapsulation pressure and temperature of these inclusions in diamonds.
Geochemical Perspectives Letters, Vol. 10, pp. 51-55.
Mantle
redox
Abstract: Among redox sensitive elements, carbon is particularly important because it may have been a driver rather than a passive recorder of Earth’s redox evolution. The extent to which the isotopic composition of carbon records the redox processes that shaped the Earth is still debated. In particular, the highly reduced deep mantle may be metal-saturated, however, it is still unclear how the presence of metallic phases in?uences the carbon isotopic compositions of super-deep diamonds. Here we report ab initio results for the vibrational properties of carbon in carbonates, diamond, and Fe3C under pressure and temperature conditions relevant to super-deep diamond formation. Previous work on this question neglected the effect of pressure on the equilibrium carbon isotopic fractionation between diamond and Fe3C but our calculations show that this assumption overestimates the fractionation by a factor of ~1.3. Our calculated probability density functions for the carbon isotopic compositions of super-deep diamonds derived from metallic melt can readily explain the very light carbon isotopic compo- sitions observed in some super-deep diamonds. Our results therefore support the view that metallic phases are present during the formation of super-deep diamonds in the mantle below ~250 km.
Earth and Planetary Science Letters, Vol. 519, pp. 1-11.
Mantle
olivine
Abstract: Velocity and density jumps across the 410-km seismic discontinuity generally indicate olivine contents of ?30 to 50 vol.% on the basis of the elastic properties of anhydrous olivine and wadsleyite, which is considerably less than the ?60% olivine in the widely accepted pyrolite model for the upper mantle. A possible explanation for this discrepancy is that water dissolved in olivine and wadsleyite affects their elastic properties in ways that can reconcile the pyrolitic model with seismic observations. In order to more fully constrain the olivine content of the upper mantle near the 410-km discontinuity, and to place constraints on the mantle water content at this depth, we determined the full elasticity of hydrous wadsleyite at the P-T conditions of the discontinuity based on density functional theory calculations. Together with previous determinations for the effect of water on olivine elasticity, we simultaneously modeled the density and seismic velocity jumps (??, , ) across the olivine-wadsleyite transition. Our models allow for several scenarios that can well reproduce the density and seismic velocity jumps across the 410-km discontinuity when compared to globally averaged seismic models. When the water content of olivine and wadsleyite is assumed to be equal as in a simple binary system, our modeling indicates a best fit for low water contents (<0.1 wt.%) with an olivine proportion of ?50%, suggesting a relatively dry, non-pyrolitic mantle at depths of the 410-km discontinuity. However, our modeling can be reconciled with a pyrolitic mantle if the water content in wadsleyite is ?0.9 wt.% and that in olivine is at its storage capacity of ?500-1500 ppm. The result would be consistent with a hydrous melt phase produced at depths just above the phase transition.
Abstract: Diamonds are key messenger from the deep Earth because someare sourced from the longest isolated and deepest accessible regions of the Earth’s mantle. They are prime recorders of the carbon isotopic compositionof the Earth. The C isotope composition (d13C) of natural diamonds showsa widevariationfrom -41‰ to +3‰ with the primary mode at -5 ± 3‰ [1]. In comparison, the d13C values of chondrites and other planetary bodies range between -26‰ and -15‰ [2]. It is possible that some of the low d13C values were inherited from the Earth’s building blocks,but this is unlikely to be the sole explanation for all low d13C values that can reach as low as -41‰. Organic matter at the Earth’s surface that has low d13C values[3] has been regarded as a possible origin for low d13C values. However, organic carbon is usually accompanied by carbonate with higher d13C values (~0 ‰),and it is not clear why this d13C value does not appear frequently in diamonds. Low d13C diamonds were also formed by deposition from C-O-H fluids,but the equilibrium fractionationinvolved between diamonds and fluids issmall at mantle temperatures [1] and the low d13C values of diamonds can only be achieved after extensive Rayleigh distillation. One unique feature of the Earth isactive plate tectonics driven by mantle convection. Relatively oxidized iron and carbon species at the surface, such as carbonate, Fe2+-and Fe3+-bearing silicatesand oxides, are transported to the deep mantle by subducted slabs and strongly involved inthe redox reactions that generatediamonds [4]. The extent to which the isotopic compositionof C duringdiamond formation recordsredox processes that shaped the Earth is still controversial. Here we report onvibration properties of C andFe at high pressure in carbonates, diamond and Fe3C,based on nuclear resonant inelastic X-ray scattering measurements and density functional theory calculationsand further calculate equilibrium C isotope fractionations among these C-bearing species. Our results demonstrate that redox reactions in subducted slabs could generate eclogitic diamonds with d13C values as low as -41‰ if C in diamonds was sourced from the oxidation of a Fe-C liquid. The large C isotopic fractionation and potentially fast separation between diamonds and a Fe-C melt could enable diamond formation as high as 2%with d13C lower than -40‰.
Earth and Planetary Science Letters, Vol. 519, pp. 1-11.
Mantle
boundary
Abstract: Velocity and density jumps across the 410-km seismic discontinuity generally indicate olivine contents of ?30 to 50 vol.% on the basis of the elastic properties of anhydrous olivine and wadsleyite, which is considerably less than the ?60% olivine in the widely accepted pyrolite model for the upper mantle. A possible explanation for this discrepancy is that water dissolved in olivine and wadsleyite affects their elastic properties in ways that can reconcile the pyrolitic model with seismic observations. In order to more fully constrain the olivine content of the upper mantle near the 410-km discontinuity, and to place constraints on the mantle water content at this depth, we determined the full elasticity of hydrous wadsleyite at the P-T conditions of the discontinuity based on density functional theory calculations. Together with previous determinations for the effect of water on olivine elasticity, we simultaneously modeled the density and seismic velocity jumps (??, , ) across the olivine-wadsleyite transition. Our models allow for several scenarios that can well reproduce the density and seismic velocity jumps across the 410-km discontinuity when compared to globally averaged seismic models. When the water content of olivine and wadsleyite is assumed to be equal as in a simple binary system, our modeling indicates a best fit for low water contents (<0.1 wt.%) with an olivine proportion of ?50%, suggesting a relatively dry, non-pyrolitic mantle at depths of the 410-km discontinuity. However, our modeling can be reconciled with a pyrolitic mantle if the water content in wadsleyite is ?0.9 wt.% and that in olivine is at its storage capacity of ?500-1500 ppm. The result would be consistent with a hydrous melt phase produced at depths just above the phase transition.
Minerals MDPI, Vol. 10, 1117, doi:10.3390/ min10121117 20p. Pdf
China
deposit - Bayan Obo
Abstract: The Bayan Obo rare earth element (REE) deposit in Inner Mongolia, northern China, is the largest REE deposit in the world, whose mineralization process remains controversial. There are dozens of carbonatite dykes that are tightly related to the deposit. Here we report the petrological and mineralogical characteristics of a typical dolomite carbonatite dyke near the deposit. The dolomite within the dyke experienced intense post-emplacement fluids metasomatism as evidenced by the widespread hydrothermal REE-bearing minerals occurring along the carbonate mineral grains. REE contents of bulk rocks and constituent dolomite minerals (>90 vol.%) are 1407-4184 ppm and 63-152 ppm, respectively, indicating that dolomite is not the dominant mineral controlling the REE budgets of the dyke. There are three types of apatite in the dyke: Type 1 apatite is the primary apatite and contains REE2O3 at 2.35-4.20 wt.% and SrO at 1.75-2.19 wt.%; Type 2 and Type 3 apatites are the products of replacement of primary apatite. The REE2O3 (6.10-8.21 wt.%) and SrO (2.83-3.63 wt.%) contents of Type 2 apatite are significantly elevated for overprinting of REE and Sr-rich fluids derived from the carbonatite. Conversely, Type 3 apatite has decreased REE2O3 (1.17-2.35 wt.%) and SrO (1.51-1.99 wt.%) contents, resulting from infiltration of fluids with low REE and Na concentrations. Our results on the dyke suggest that post-magmatic fluids expelled from the carbonatitic melts dominated the REE mineralization of the Bayan Obo deposit, and a significant fluid disturbance occurred but probably provided no extra REEs to the deposit.
Earth and Planetary Science Letters, Vol. 554, doi:10.1016/ j.epsl.2020. 116626 12p. Pdf
Mantle
water
Abstract: The mantle transition zone (MTZ) is potentially a geochemical water reservoir because of the high H2O solubility in its dominant minerals, wadsleyite and ringwoodite. Whether the MTZ is wet or dry fundamentally impacts our understanding of the deep-water distribution, geochemical recycling, and the pattern of mantle convection. However, the water content in the MTZ inferred from previous studies remains disputed. Seismic observations such as velocity anomalies were used to evaluate the water content in the MTZ, but the hydration effect on the velocities of MTZ minerals under appropriate pressure (P) and temperature (T) conditions is poorly constrained. Here we investigated the elastic properties and velocities of hydrous ringwoodite at high P-T conditions using first-principles calculations. Our results show that the hydration effects on elastic moduli and velocities of ringwoodite are significantly reduced by pressure but strongly enhanced by temperature. The incorporation of 1.0 wt% water into ringwoodite decreases the compressional and shear velocities of the pyrolitic mantle by ?1.0% and ?1.4% at the conditions of MTZ, respectively. Using results from seismic tomography and together with the topography of the 660-km discontinuity, we evaluate the global distribution of water in the lower MTZ. We find that about 80% of the MTZ can be explained by varying water content and temperature, however, the remaining 20% requires the presence of high-velocity heterogeneities such as harzburgite. Our models suggest an average water concentration of ?0.2 wt% in the lower MTZ, with an interregional variation from 0 to 0.9 wt%. Together with our previous work, we conclude that the water concentration in the MTZ likely decreases with depth globally and the whole MTZ contains the equivalent of about one ocean mass of water.
Geochimica et Cosmochimica Acta, Vol. 294, pp. 215-231. pdf
Mantle
bridgmanite
Abstract: The isotopic compositions of iron in major mantle minerals may record chemical exchange between deep-Earth reservoirs as a result of early differentiation and ongoing plate tectonics processes. Bridgmanite (Bdg), the most abundant mineral in the Earth’s lower mantle, can incorporate not only Al but also Fe with different oxidation states and spin states, which in turn can influence the distribution of Fe isotopes between Bdg and ferropericlase (Fp) and between the lower mantle and the core. In this study, we combined first-principles calculations with high-pressure nuclear resonant inelastic X-ray scattering measurements to evaluate the effects of Fe site occupancy, valence, and spin states at lower-mantle conditions on the reduced Fe partition function ratio (?-factor) of Bdg. Our results show that the spin transition of octahedral-site (B-site) Fe3+ in Bdg under mid-lower-mantle conditions generates a +0.09‰ increase in its ?-factor, which is the most significant effect compared to Fe site occupancy and valence. Fe2+-bearing Bdg varieties have smaller ?-factors relative to Fe3+-bearing varieties, especially those containing B-site Fe3+. Our models suggest that Fe isotopic fractionation between Bdg and Fp is only significant in the lowermost mantle due to the occurrence of low-spin Fe2+ in Fp. Assuming early segregation of an iron core from a deep magma ocean, we find that neither core formation nor magma ocean crystallization would have resulted in resolvable Fe isotope fractionation. In contrast, Fe isotopic fractionation between low-spin Fe3+-bearing Bdg/Fe2+-bearing Fp and metallic iron at the core-mantle boundary may have enriched the lowermost mantle in heavy Fe isotopes by up to +0.20‰.
Journal of Asian Earth Sciences, Vol. 172, pp. 56-65.
China, Mongolia
deposit - Bayan Obo
Abstract: In the Bayan Obo REE deposit in Inner Mongolia, Northern China, three major orebodies are hosted in dolomite marble of the Bayan Obo Group. There are carbonatite dikes in the ore district. Apatite is a common accessary mineral in the ore-hosting dolomite marble (DM apatite) and in carbonatite dikes (IC apatite). These two types of apatite are both fluorapatite, and have low SiO2, uniform P2O5, and variable CaO contents. Total REY (REEs?+?Y) contents are correlated with Na2O contents, indicating that REY of both types of apatite enter lattice via the substitution reaction: Na+ + (REY)3+ = 2Ca2+. These features, combined with high REY (6230-18,906?ppm) and Sr (9653-17,200?ppm) contents of DM apatite, indicate that DM apatite likely had a carbonatite origin. Some DM apatite grains are partially replaced by albite and quartz. Fluid inclusions crosscutting both apatite and albite or quartz indicate that they formed later than quartz and albite replacement. The back-scattered electron images show that DM apatite grains contain many micro-pores (fluid inclusions), and monazite inclusions formed from the fluid inclusions. However, no monazite inclusions are observed within quartz and albite, excluding the possibility that the monazite inclusions were precipitated directly from the fluids. The monazite inclusions were therefore formed during fluid-induced dissolution-reprecipitation processes, where DM apatite served as the source of LREEs. This also explains the depletion of some LREEs in DM apatite. The formation of monazite inclusions in apatite requires fluids with relatively low Na and Si concentrations, different from the fluids responsible for quartz and albite replacement. DM apatite was affected by two stages of fluid activities: the first stage of metasomatism by alkaline fluids that were likely derived from carbonatite magmas when the deposit first formed (represented by quartz and albite replacement), followed by a second stage of modification that caused LREEs depletion and the formation of new REE minerals. Thus, the Bayan Obo REE ore deposit was modified by a significant thermal event after the formation, which provided negligible or only small amounts of REEs.
Abstract: The oxygen fugacity of the upper mantle is 3-4 orders of magnitude higher than that of the lower mantle and this has been attributed to Fe2 + disproportionating into Fe3 + plus Fe0 at pressures > 24 GPa. The upper mantle might therefore have been expected to have evolved to more oxidizing compositions through geological time, but it appears that the oxygen fugacity of the upper mantle has remained constant for the last 3.5 billion years. Thus, it indicates that the mantle has been actively buffered from the accumulation of Fe3 +, and that this is linked to oxidation of diamond to carbonate coupled with reduction of Fe3 + to Fe2 +. When subducted plates penetrate into the lower mantle, compensational upwelling transports bridgmanite into the transition zone, where it breaks down to ringwoodite and majorite, releasing the ferric iron. The system returns to equilibrium through oxidation of diamond. Early in Earth history, diamond may have been enriched at the base of the transition zone in the Magma Ocean, because it is denser than peridotite melts at depths shallower than 660 km, and it is more buoyant below. Ongoing oxidation of diamond forms carbonate, leading to relatively high carbonate concentrations in the source of ocean island basalts.
Contributions to Mineralogy and Petrology, Vol. 169, 19p.
Russia, Kazakhstan
Diamondiferous tourmaline
Abstract: Tourmaline was synthesized in the system MgO-Al2O3-B2O3-SiO2-KCl-NaCl-H2O from an oxide mixture and excess fluid at 500-700 °C and 0.2-4.0 GPa to investigate the effect of pressure, temperature, and fluid composition on the relative incorporation of Na and K in dravitic tourmaline. Incorporation of K at the X-site increases with pressure, temperature, and KCl concentration; a maximum of 0.71 K pfu (leaving 0.29 X-vacant sites pfu) was incorporated into K-dravite synthesized at 4.0 GPa, 700 °C from a 4.78 m KCl, Na-free fluid. In contrast, Na incorporation depends predominately on fluid composition, rather than pressure or temperature; dravite with the highest Na content of 1.00 Na pfu was synthesized at 0.4 GPa and 700 °C from a 3.87 m NaCl and 1.08 m KCl fluid. All synthesized crystals are zoned, and the dominant solid solution in the Na- and K-bearing system is between magnesio-foitite [?(Mg2Al)Al6Si6O18(BO3)3(OH)3OH] and dravite [NaMg3Al6Si6O18(BO3)3(OH)3(OH)], with the dravitic component increasing with the concentration of Na in the fluid. In the K-bearing, Na-free system, the dominant solid solution is between magnesio-foitite and K-dravite [KMg3Al6Si6O18(BO3)3(OH)3(OH)], with the K-dravitic component increasing with pressure, temperature, and the concentration of K in the fluid. The unit-cell volume of tourmaline increases with K incorporation from 1555.1(3) to 1588.1(2) Å3, reflecting the incorporation of the relatively large K+ ion. Comparison of our results to the compositional data for maruyamaite (K-dominant tourmaline) from the ultrahigh-pressure rocks of the Kokchetav Massif in Kazakhstan suggests that the latter was formed in a K-rich, Na-poor environment at ultrahigh-pressure conditions near the diamond-stability field.
Contributions to Mineralogy and Petrology, Vol. 171, pp. 1-12.
Europe
Bohemian
Abstract: A unique assemblage including kumdykolite and kokchetavite, polymorphs of albite and K-feldspar, respectively, together with cristobalite, micas, and calcite has been identified in high-pressure granulites of the Orlica-Snieznik dome (Bohemian Massif) as the product of partial melt crystallization in preserved nanogranites. Previous reports of both kumdykolite and kokchetavite in natural rocks are mainly from samples that passed through the diamond stability field. However, because the maximum pressure recorded in these host rocks is <3 GPa, our observations indicate that high pressure is not required for the formation of kumdykolite and kokchetavite, and their presence is not therefore an indicator of ultrahigh-pressure conditions. Detailed microstructural and microchemical investigation of these inclusions indicates that such phases should instead be regarded as (1) a direct mineralogical criteria to identify former melt inclusions with preserved original compositions, including H2O and CO2 contents and (2) indicators of rapid cooling of the host rocks. Thus, the present study provides novel criteria for the interpretation of melt inclusions in natural rocks and allows a more rigorous characterization of partial melts during deep subduction to mantle depth as well as their behavior on exhumation.
Earth and Planetary Science Letters, Vol. 454, pp. 121-131.
Europe, Czech Republic
Bohemian Massif
Abstract: Carbonatites are peculiar magmatic rocks with mantle-related genesis, commonly interpreted as the products of melting of CO2-bearing peridotites, or resulting from the chemical evolution of mantle-derived magmas, either through extreme differentiation or secondary immiscibility. Here we report the first finding of anatectic carbonatites of crustal origin, preserved as calcite-rich polycrystalline inclusions in garnet from low-to-medium pressure migmatites of the Oberpfalz area, SW Bohemian Massif (Central Europe). These inclusions originally trapped a melt of calciocarbonatitic composition with a characteristic enrichment in Ba, Sr and LREE. This interpretation is supported by the results of a detailed microstructural and microchemical investigation, as well as re-melting experiments using a piston cylinder apparatus. Carbonatitic inclusions coexist in the same cluster with crystallized silicate melt inclusions (nanogranites) and COH fluid inclusions, suggesting conditions of primary immiscibility between two melts and a fluid during anatexis. The production of both carbonatitic and granitic melts during the same anatectic event requires a suitable heterogeneous protolith. This may be represented by a sedimentary sequence containing marble lenses of limited extension, similar to the one still visible in the adjacent central Moldanubian Zone. The presence of CO2-rich fluid inclusions suggests furthermore that high CO2 activity during anatexis may be required to stabilize a carbonate-rich melt in a silica-dominated system. This natural occurrence displays a remarkable similarity with experiments on carbonate-silicate melt immiscibility, where CO2 saturation is a condition commonly imposed.
Earth and Planetary Science Letters, Vol. 454, pp. 121-131.
Mantle
carbonatites
Abstract: Carbonatites are peculiar magmatic rocks with mantle-related genesis, commonly interpreted as the products of melting of CO2-bearing peridotites, or resulting from the chemical evolution of mantle-derived magmas, either through extreme differentiation or secondary immiscibility. Here we report the first finding of anatectic carbonatites of crustal origin, preserved as calcite-rich polycrystalline inclusions in garnet from low-to-medium pressure migmatites of the Oberpfalz area, SW Bohemian Massif (Central Europe). These inclusions originally trapped a melt of calciocarbonatitic composition with a characteristic enrichment in Ba, Sr and LREE. This interpretation is supported by the results of a detailed microstructural and microchemical investigation, as well as re-melting experiments using a piston cylinder apparatus. Carbonatitic inclusions coexist in the same cluster with crystallized silicate melt inclusions (nanogranites) and COH fluid inclusions, suggesting conditions of primary immiscibility between two melts and a fluid during anatexis. The production of both carbonatitic and granitic melts during the same anatectic event requires a suitable heterogeneous protolith. This may be represented by a sedimentary sequence containing marble lenses of limited extension, similar to the one still visible in the adjacent central Moldanubian Zone. The presence of CO2-rich fluid inclusions suggests furthermore that high CO2 activity during anatexis may be required to stabilize a carbonate-rich melt in a silica-dominated system. This natural occurrence displays a remarkable similarity with experiments on carbonate-silicate melt immiscibility, where CO2 saturation is a condition commonly imposed. In conclusion, this study shows how the investigation of partial melting through melt inclusion studies may unveil unexpected processes whose evidence, while preserved in stiff minerals such as garnet, is completely obliterated in the rest of the rock due to metamorphic re-equilibration. Our results thus provide invaluable new insights into the processes which shape the geochemical evolution of our planet, such as the redistribution of carbon and strategic metals during orogenesis.
Annual Review of Earth and Planetary Sciences, Vol. 43, pp. 273-298.
Mantle
Carbon
Abstract: Pyrogenic carbon (PyC; includes soot, char, black carbon, and biochar) is produced by the incomplete combustion of organic matter accompanying biomass burning and fossil fuel consumption. PyC is pervasive in the environment, distributed throughout the atmosphere as well as soils, sediments, and water in both the marine and terrestrial environment. The physicochemical characteristics of PyC are complex and highly variable, dependent on the organic precursor and the conditions of formation. A component of PyC is highly recalcitrant and persists in the environment for millennia. However, it is now clear that a significant proportion of PyC undergoes transformation, translocation, and remineralization by a range of biotic and abiotic processes on comparatively short timescales. Here we synthesize current knowledge of the production, stocks, and fluxes of PyC as well as the physical and chemical processes through which it interacts as a dynamic component of the global carbon cycle.
