Hello Guest User, You are visiting this website from a computer with an IP address of 162.158.79.247 with the name of '?' since Fri Jan 15, 2021 at 12:34:46 PM PT for approx. 0 minutes now.
SDLRC - Scientific Articles all years by Author - Gr+
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.
Sort Order
References are sorted by the "author" name and when the reference was posted to the compilation.
Most Recent
If the reference code is highlighted yellow, the reference was made available through the most recent monthly compilation of new literature. Use this to check out new references. When new references are posted, we make it our priority to track down an online link and obtain an abstract. With regard to older references, tracking down an abstract and an online link is a work in progress.
Link to external location of article:
If the title has a link, it means we have found a location online where you can either retrieve the full article free, or purchase access to it. The Sheahan Diamond Literature Service is not a technical article procurement service; if you want a restricted article, you must deal directly with the vendor who controls the copyright to the article.
Searching this page for a specific term or author
In your Firefox browser click Edit in the menu bar and then Find. In the Find box that shows up at the bottom of the web page enter your search term. Firefox will highlight all occurrences. This is particularly helpful when the author you are seeking was not the lead author by whom the compilation is sorted.
Sending or sharing a reference
The left column (Posted/Published) has an embedded hyperlink for each reference. In Firefox, if you right click on it, you can obtain the link url for that reference's location within the page, which you can copy and paste into an email or any other document. You can also use the "share this link" option to tweet, facebook etc the link.
Abstract: This Tajno alkaline massif (together with the nearby Elk 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 eNd(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 d18O and d13C values.
Abstract: The problem of the existence of the asthenosphere for old Precambrian cratons is still discussed. In order to study the seismic lithosphere-asthenosphere boundary (LAB) beneath the Baltic Shield, we used records of nine local earthquakes with magnitudes ranging from 2.7 to 5.9. To model the LAB, original data were corrected for topography and Moho depth using a reference model with a 46-km-thick crust. For two northern events at Spitsbergen and Novaya Zemlya, we observe a low-velocity layer, 60-70-km-thick asthenosphere, and the LAB beneath Barents Sea was found at depth of c. 200 km. Sections for other events show continuous first arrivals of P-waves with no evidence for "shadow zone" in the whole range of registration, which could either be interpreted as the absence of the asthenosphere beneath the central part of the Baltic Shield, or that the LAB in this area occurs deeper (>200 km). The relatively thin low-velocity layer found beneath southern Sweden, 15 km below the Moho, could be interpreted as small-scale lithospheric heterogeneities, rather than asthenosphere. Differentiation of the lower lithosphere velocities beneath the Baltic Shield could be interpreted as regional heterogeneity or as anisotropy of the Baltic Shield lithosphere, with high velocities approximately in the east-west direction, and slow velocities approximately in the south-north direction.
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: 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].
Geochimica et Cosmochimica Acta, in press available, doi.org/101016 /j.gca.2020.07.013 45p. Pdf
Canada, Northwest Territories
deposit - Lac de Gras
Abstract: Whether hydrogen incorporated in nominally anhydrous mantle minerals plays a role in the strength and longevity of the thick cratonic lithosphere is a matter of debate. In particular, the percolation of hydrogen-bearing melts and fluids could potentially add hydrogen to the mantle lithosphere, weaken its olivines (the dominant mineral in mantle peridotite), and cause delamination of the lithosphere's base. The influence of metasomatism on hydrogen contents of cratonic mantle minerals can be tested in mantle xenoliths from the Slave Craton (Canada) because they show extensive evidence for metasomatism of a layered cratonic mantle. Minerals from mantle xenoliths from the Diavik mine in the Lac de Gras kimberlite area located at the center of the Archean Slave craton were analyzed by FTIR for hydrogen contents. The 18 peridotites, two pyroxenites, one websterite and one wehrlite span an equilibration pressure range from 3.1 to 6.6 GPa and include samples from the shallow (= 145 km), oxidized ultra-depleted layer; the deeper (~145-180 km), reduced less depleted layer; and an ultra-deep (= 180 km) layer near the base of the lithosphere. Olivine, orthopyroxene, clinopyroxene and garnet from peridotites contain 30 - 145, 110 - 225, 105 - 285, 2 - 105 ppm H2O, respectively. Within each deep and ultra-deep layer, correlations of hydrogen contents in minerals and tracers of metasomatism (for example light over heavy rare-earth-element ratio (LREE/HREE), high-field-strength-element (HFSE) content with equilibration pressure) can be explained by a chromatographic process occurring during the percolation of kimberlite-like melts through garnet peridotite. The hydrogen content of peridotite minerals is controlled by the compositions of the evolving melt and of the minerals and by mineral/melt partition coefficients. At the beginning of the process, clinopyroxene scavenges most of the hydrogen and garnet most of the HFSE. As the melt evolves and becomes enriched in hydrogen and LREE, olivine and garnet start to incorporate hydrogen and pyroxenes become enriched in LREE. The hydrogen content of peridotite increases with decreasing depth, overall (e.g., from 75 to 138 ppm H2O in the deep peridotites). Effective viscosity calculated using olivine hydrogen content for the deepest xenoliths near the lithosphere-asthenosphere boundary overlaps with estimates of asthenospheric viscosities. These xenoliths cannot be representative of the overall cratonic root because the lack of viscosity contrast would have caused basal erosion of lithosphere. Instead, metasomatism must be confined in narrow zones channeling kimberlite melts through the lithosphere and from where xenoliths are preferentially sampled. Such localized metasomatism by hydrogen-bearing melts therefore does not necessarily result in delamination of the cratonic root.
Geochimica et Cosmochimica Acta, Vol. 286, pp. 29-83. pdf
Canada, Northwest Territories
xenoliths
Abstract: Whether hydrogen incorporated in nominally anhydrous mantle minerals plays a role in the strength and longevity of the thick cratonic lithosphere is a matter of debate. In particular, the percolation of hydrogen-bearing melts and fluids could potentially add hydrogen to the mantle lithosphere, weaken its olivines (the dominant mineral in mantle peridotite), and cause delamination of the lithosphere's base. The influence of metasomatism on hydrogen contents of cratonic mantle minerals can be tested in mantle xenoliths from the Slave Craton (Canada) because they show extensive evidence for metasomatism of a layered cratonic mantle. Minerals from mantle xenoliths from the Diavik mine in the Lac de Gras kimberlite area located at the center of the Archean Slave craton were analyzed by FTIR for hydrogen contents. The 18 peridotites, two pyroxenites, one websterite and one wehrlite span an equilibration pressure range from 3.1 to 6.6 GPa and include samples from the shallow (=145?km), oxidized ultra-depleted layer; the deeper (~145-180?km), reduced less depleted layer; and an ultra-deep (=180?km) layer near the base of the lithosphere. Olivine, orthopyroxene, clinopyroxene and garnet from peridotites contain 30-145, 110-225, 105-285, 2-105?ppm H2O, respectively. Within each deep and ultra-deep layer, correlations of hydrogen contents in minerals and tracers of metasomatism (for example light over heavy rare-earth-element ratio (LREE/HREE), high-field-strength-element (HFSE) content with equilibration pressure) can be explained by a chromatographic process occurring during the percolation of kimberlite-like melts through garnet peridotite. The hydrogen content of peridotite minerals is controlled by the compositions of the evolving melt and of the minerals and by mineral/melt partition coefficients. At the beginning of the process, clinopyroxene scavenges most of the hydrogen and garnet most of the HFSE. As the melt evolves and becomes enriched in hydrogen and LREE, olivine and garnet start to incorporate hydrogen and pyroxenes become enriched in LREE. The hydrogen content of peridotite increases with decreasing depth, overall (e.g., from 75 to 138?ppm H2O in the deep peridotites). Effective viscosity calculated using olivine hydrogen content for the deepest xenoliths near the lithosphere-asthenosphere boundary overlaps with estimates of asthenospheric viscosities. These xenoliths cannot be representative of the overall cratonic root because the lack of viscosity contrast would have caused basal erosion of lithosphere. Instead, metasomatism must be confined in narrow zones channeling kimberlite melts through the lithosphere and from where xenoliths are preferentially sampled. Such localized metasomatism by hydrogen-bearing melts therefore does not necessarily result in delamination of the cratonic root.
Hydrothermal oxygen diffusion in diopside at 1 KB, 900-1200C, a comparison with O diffusion in forsterite, and constraints on OI disequil. in peridotitenodules
Terra, Abstracts of Experimental mineralogy, petrology and, Vol. 2, December abstracts p. 72
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.
Mineralogy and Petrology, Vol. 110, 2, pp. 399-420.
Indonesia
Megacrysts
Abstract: Zircon megacrysts (± gem corundum) appear in basalt fields of Indo-Pacific origin over a 12,000 km zone (ZIP) along West Pacific continental margins. Age-dating, trace element, oxygen and hafnium isotope studies on representative zircons (East Australia-Asia) indicate diverse magmatic sources. The U-Pb (249 to 1 Ma) and zircon fission track (ZFT) ages (65 to 1 Ma) suggest thermal annealing during later basalt transport, with?
Cathodluminescence of colored diamonds by transmissionelectronmicroscopy
Geological Association of Canada (GAC)/Mineralogical Association of Canada (MAC) Vancouver 90 Program with Abstracts, Held May 16-18, Vol. 15, p. A50. Abstract
Doklady Earth Sciences, Vol. 465, 2, pp. 1297-1301.
Russia, Siberia
Deposit - Malokuonapskaya
Abstract: The U-Pb (SHRIMP) age was determined for zircons collected from 26 observation and sampling sites of diamonds and index minerals in the northeastern Siberian Platform. This part of the region hosts 15 low-diamondiferous Paleozoic and Mesozoic kimberlite fields, excluding the near economic Triassic Malokuonapskaya pipe in the Kuranakh field. Four epochs of kimberlite formation (Silurian, Late Devonian to Early Carboniferous, Middle to Late Triassic, and Middle to Late Jurassic) of the Siberian Platform, including its northeastern part, are confirmed as a result of our studies. Most observation points, including economic Quaternary diamond placers, contain Middle to Late Triassic zircons, which confirms the abundant Late Triassic volcanism in this region. The positive correlation of diamonds and major index minerals of kimberlites (mostly, garnets) at some observation sites indicates the possible Triassic age of the predictable diamondiferous kimberlites.
Abstract: Modern plate tectonics may have gotten under way as early as 3.2 billion years ago, about 400 million years earlier than scientists thought. That, in turn, suggests that the movement of large pieces of Earth’s crust could have played a role in making the planet more hospitable to life. Geologist Alec Brenner of Harvard University and his colleagues measured the magnetic orientations of iron-bearing minerals in the Honeyeater Basalt, a layer of rock that formed between 3.19 billion and 3.18 billion years ago. The basalt is part of the East Pilbara Craton, an ancient bit of continent in Western Australia that includes rocks as old as 3.5 billion years. This craton, the researchers found, was on the move between 3.35 billion and 3.18 billion years ago, drifting around the planet at a rate of at least 2.5 centimeters per year. That’s a speed comparable to modern plate motions, the team reports April 22 in Science Advances.
Joint seismic geodynamic mineral physical modeling of African geodynamics: a reconciliation of deep mantle convection with surface geophysical constraints.
Earth and Planetary Science Letters, Vol. 295, 3-4, pp. 329-341.
A Tertiary asthenospheric flow beneath the southern French Massif Central indicated by upper mantle seismic anisotropy and related to west mediterranean extension.
Earth and Planetary Science Letters, Vol. 202, 1, pp.31-47.
Journal of Petrology , Vol. 60, 6, pp. 1119--1134.
India
carbonatite
Abstract: There are disparate views about the origin of global rift- or plume-related carbonatites. The Amba Dongar carbonatite complex, Gujarat, India, which intruded into the basalts of the Deccan Large Igneous Province (LIP), is a typical example. On the basis of new comprehensive major and trace element and Sr-Nd-Pb isotope data, we propose that low-degree primary carbonated melts from off-center of the Deccan-Réunion mantle plume migrate upwards and metasomatize part of the subcontinental lithospheric mantle (SCLM). Low-degree partial melting (~2%) of this metasomatized SCLM source generates a parental carbonated silicate magma, which becomes contaminated with the local Archean basement during its ascent. Calcite globules in a nephelinite from Amba Dongar provide evidence that the carbonatites originated by liquid immiscibility from a parental carbonated silicate magma. Liquid immiscibility at crustal depths produces two chemically distinct, but isotopically similar magmas: the carbonatites (20% by volume) and nephelinites (80% by volume). Owing to their low heat capacity, the carbonatite melts solidified as thin carbonate veins at crustal depths. Secondary melting of these carbonate-rich veins during subsequent rifting generated the carbonatites and ferrocarbonatites now exposed at Amba Dongar. Carbonatites, if formed by liquid immiscibility from carbonated silicate magmas, can inherit a wide range of isotopic signatures that result from crustal contamination of their parental carbonated silicate magmas. In rift or plume-related settings, they can, therefore, display a much larger range of isotope signatures than their original asthenosphere or mantle plume source.
South African Journal of Geology, Vol. 121, pp. 271-286.
Africa, Mozambique
geodynamics
Abstract: Major, trace, radiogenic isotope and stable isotope data from lavas along the northeastern coast of Mozambique are described. The whole rock composition data demonstrate that the rocks are dominantly andesitic with compositions typical of calc-alkaline volcanic rocks from arc environments. SHRIMP U/Pb data from zircons indicate that the zircons are xenocrystic, having ages of between 500 Ma and 660 Ma, with the age of the lava constrained by Rb/Sr data at ~184 Ma. Strontium, Nd and Pb radiogenic isotope data support an interpretation of extensive mixing between a Karoo age basaltic magma (dolerite) from Antarctica and continental crust similar in composition to the Mozambique basement. Oxygen isotope data also imply a significant crustal contribution to the lavas. Possible tectonic settings for the lavas are at the margin of a plume or from a locally restricted compressional setting during Gondwana breakup processes.
Grantham, G.H., Manhica, A.D.S.T., Armstrong, R.A., Kruger, F.J., Loubser, M.
New SHRIMP, Rb/Sr and Sm/Nd isotope and whole rock chemical dat a from central Mozambique and western Dronning Maud Land: implications for eastern Kalahari
Journal of African Earth Sciences, Vol. 59, 1, pp.74-100.
Abstract: We report on pipe-like bodies and dikes of carbonate rocks related to sodic alkaline intrusions and amphibole mantle peridotites in the Ivrea zone (European Southern Alps). The carbonate rocks have bulk trace-element concentrations typical of low-rare earth element carbonatites interpreted as cumulates of carbonatite melts. Faintly zoned zircons from these carbonate rocks contain calcite inclusions and have trace-element compositions akin to those of carbonatite zircons. Laser ablation-inductively coupled plasma-mass spectrometry U-Pb zircon dating yields concordant ages of 187 ± 2.4 and 192 ± 2.5 Ma, coeval with sodic alkaline magmatism in the Ivrea zone. Cross-cutting relations, ages, as well as bulk and zircon geochemistry indicate that the carbonate rocks are carbonatites, the first ones reported from the Alps. Carbonatites and alkaline intrusions are comagmatic and were emplaced in the nascent passive margin of Adria during the Early Jurassic breakup of Pangea. Extension caused partial melting of amphibole-rich mantle domains, yielding sodic alkaline magmas whose fractionation led to carbonatite-silicate melt immiscibility. Similar occurrences in other rifts suggest that small-scale, sodic and CO2-rich alkaline magmatism is a typical result of extension and decompression-driven reactivation of amphibole-bearing lithospheric mantle during passive continental breakup and the evolution of magma-poor rifts.
Simandl, G.J., Paradis, S., Stone, R.S., Fajber, R., Kressall, R.D., Grattan, K., Crozier, J., Simandl, L.J.
Applicablity of handheld X-ray fluroescence spectrometry in the exploration and development of carbonatite related niobium deposits: a case study of the Aley carbonatite, British Columbia, Canada.
Geochemistry: Exploration, Environment, Analysis, Vol. 14, 3, pp. 211-221.
Symposium on critical and strategic materials, British Columbia Geological Survey Paper 2015-3, held Nov. 13-14, pp. 211-218.
Technology
Rare earths
Abstract: Quantitative Evaluation of Materials by Scanning electron microscopy (QEMSCAN®) was used to assess carbonatite indicator minerals in fl uvial sediments from the drainage area of the Aley carbonatite, in north-central British Columbia. QEMSCAN® is a viable method for rapid detection and characterization of carbonatite indicator minerals with minimal processing other than dry sieving. Stream sediments from directly above, and up to 11 km downstream, of the carbonatite deposit were selected for this indicator mineral study. The geology of the Aley carbonatite is described by Mäder (1986), Kressal et al. (2010), McLeish (2013), Mackay and Simandl (2014), and Chakhmouradian et al. (2015). Traditional indicator mineral exploration methods use the 0.25-2.0 mm size fraction of unconsolidated sediments (Averill, 2001, 2014; McCurdy, 2006, 2009; McClenaghan, 2011, 2014). Indicator minerals are detectable by QEMSCAN® at particle sizes smaller than those used for hand picking (<0.25 mm). Pre-concentration (typically by shaker table) is used before heavy liquid separation, isodynamic magnetic separation, optical identifi cation using a binocular microscope, and hand picking (McClenaghan, 2011). Following additional sieving, the 0.5-1 and 1-2 mm fractions are hand picked for indicator minerals while the 0.25-0.5 mm fraction is subjected to paramagnetic separation before hand picking (Averill, 2001; McClenaghan, 2011). Hand picking indicator minerals focuses on monomineralic grains, and composite grains may be lost during processing. Composite grains are diffi cult and time consuming to hand pick and characterize using optical and Scanning Electron Microscopy (SEM) methods. A single grain mount can take 6-12 hours to chemically analyse (Layton- Matthews et al., 2014). Detailed sample analysis using the QEMSCAN® Particle Mineral Analysis routine allows for 5-6 samples to be analyzed per day. When only mineral identifi cation and mineral concentrations and counts are required, the use of a Bulk Mineral Analysis routine reduces the analysis time from ~4 hours to ~30 minutes per sample.
Journal of Geochemical Exploration, Vol. 165, pp. 159-173.
Canada, British Columbia
Geochemistry - carbonatites
Abstract: This orientation survey indicates that Quantitative Evaluation of Materials by Scanning electron microscopy (QEMSCAN®) is a viable alternative to traditional indicator mineral exploration approaches which involve complex processing followed by visual indicator mineral hand-picking with a binocular microscope. Representative polished smear sections of the 125-250 µm fraction (dry sieved and otherwise unprocessed) and corresponding Mozley C800 table concentrates from the drainages of three carbonatites (Aley, Lonnie, and Wicheeda) in the British Columbia Alkaline Province of the Canadian Cordillera were studied. Polished smear sections (26 × 46 mm slide size) contained an average of 20,000 exposed particles. A single section can be analyzed in detail using the Particle Mineral Analysis routine in approximately 3.5-4.5 h. If only mineral identification and mineral concentrations are required, the Bulk Mineral Analysis routine reduces the analytical time to 30 min. The most useful carbonatite indicator minerals are niobates (pyrochlore and columbite), REE-fluorocarbonates, monazite, and apatite. Niobate minerals were identified in the 125-250 µm fraction of stream sediment samples more than 11 km downstream from the Aley carbonatite (their source) without the need for pre-concentration. With minimal processing by Mozley C800, carbonatite indicator minerals were detected downstream of the Lonnie and Wicheeda carbonatites. The main advantages of QEMSCAN® over the traditional indicator mineral exploration techniques are its ability to: 1) analyze very small minerals, 2) quickly determine quantitative sediment composition and mineralogy by both weight percent and mineral count, 3) establish mineral size distribution within the analyzed size fraction, and 4) determine the proportions of monomineralic (liberated) grains to compound grains and statistically assess mineral associations in compound grains. One of the key advantages is that this method permits the use of indicator minerals based on their chemical properties. This is impossible to accomplish using visual identification.
in: Ferbey, T. Plouffe, A., Hickein, A.S. eds. Indicator minerals in tills and stream sediments of the Canadian Cordillera. Geological Association of Canada Special Paper,, Vol. 50, pp. 175-190.
Canada, British Columbia
carbonatite - Aley, Lonnie, Wicheeda
Abstract: This volume consists of a series of papers of importance to indicator minerals in the Canadian Cordillera. Topics include the glacial history of the Cordilleran Ice Sheet, drift prospecting methods, the evolution of survey sampling strategies, new analytical methods, and recent advances in applying indicators minerals to mineral exploration. This volume fills a notable knowledge gap on the use of indicator minerals in the Canadian Cordillera. We hope that the volume serves as a user guide, encouraging the wider application of indicator minerals by the exploration community.
Mechanisms to Explain the Loss of Heavy Minerals from Upper paleozoic Tillites of South Africa and Australia and the Late Precambrian Tillites of Australia.
Viljoen, K.S., Harris, J.W., Richardson, S.H., Gray, K.
Trace element chemistry of peridotitic garnets in diamonds from the Premier ( Cullinan) and Finsch kimberlites, South Africa: contrasting styles of mantle metasomatism.
Canadian Journal of Earth Sciences, Vol. 52, 11, pp. 980-989.
Canada, Nunavut, Baffin Island
Geomorphology
Abstract: Speckle tracking of ALOS PALSAR fine beam data from 2007-2011 are used to determine the surface motion of major ice masses on Baffin Island and Bylot Island in the southern Canadian Arctic Archipelago. Glacier velocities are low overall, with peaks of ~100 m a-1 and means of ~20-60 m a-1 common along the main trunk of many outlet glaciers. Peak velocities on Penny and Bylot Island ice caps tend to occur near the mid-sections of their primary outlet glaciers, while the fastest velocities on all other glaciers usually occur near their termini due to relatively large accumulation areas draining through narrow outlets. Estimates of ice thickness at the fronts of tidewater-terminating glaciers are combined with the velocity measurements to determine a regional dynamic discharge rate of between ~17 Mt a-1 and ~108 Mt a-1, with a mid-point estimate of ~55 Mt a-1, revising downward previous approximations. These velocities can be used as inputs for glacier flow models, and provide a baseline dataset against which future changes in ice dynamics can be detected.
Journal of Geophysical Letters, Vol. 47, e2020GL087222
Mantle
water
Abstract: The amount of water trapped in the Earth's interior has a strong effect on the evolution and dynamics of the planet, which ultimately controls the occurrence of earthquakes and volcanic eruptions. However, the distribution of water inside the Earth is not yet well understood. To study the Earth's deep interior, we make use of changes in the Earth's magnetic field to detect variations in electrical conductivity inside the planet. Electrical conductivity is a characteristic of a rock that varies with temperature and water content. Here, we present a novel methodology to estimate the amount of water in different regions of Earth's mantle. Our analysis suggests the presence of small amounts of water in the mantle underneath Europe, whereas larger amounts are expected beneath North America and northern Asia.
Abstract: Magnesium and oxygen are critical elements in the solid Earth and hydrosphere. A better understanding of the combined behavior of Mg and O isotopes will refine their use as a tracer of geochemical processes and Earth evolution. In this study, the Mg-isotope compositions of garnet and omphacite separated from well-characterized xenolithic eclogites from the Roberts Victor kimberlite pipe (South Africa) have been measured by solution multi-collector ICP-MS. The reconstructed whole-rock d26Mg values of Type I (metasomatized) eclogites range from - 0.61‰ to - 0.20‰ (Type IA) and from - 0.60‰ to - 0.30‰ (Type IB) (mean - 0.43‰ ± 0.12‰), while d26Mg of Type IIA (fresh, least metasomatized) eclogites ranges from - 1.09‰ to - 0.17‰ (mean - 0.69‰ ± 0.41‰); a Type IIB (fresh, least metasomatized) has d26Mg of - 0.37‰. Oxygen-isotope compositions of garnet were analyzed in situ by SIMS (CAMECA 1280) and cross-checked by laser fluorination. Garnets have d18O of 6.53‰ to 9.08‰ in Type IA, 6.14‰ to 6.65‰ in Type IB, and 2.34‰ to 2.91‰ in Type IIB. The variation of d26Mg and d18O in Type IA and IB eclogites is consistent with the previously proposed model for the evolution of these samples, based on major and trace elements and radiogenic isotopes. In this model, the protoliths (Type II eclogites) were metasomatized by carbonatitic to kimberlitic melts/fluids to produce first Type IA eclogites and then Type IB. Metasomatism has changed the O-isotope compositions, but the Mg-isotope compositions of Type IA are mainly controlled by the protoliths; those of Type IB eclogites reflect mixing between the protoliths and the kimberlitic melt/fluid. The combination of a large range of d26Mg and low d18O in Type II eclogites cannot be explained easily by seawater alteration of oceanic crust, interaction of carbonate/silicate sediments with oceanic crust, or partial melting of mafic rocks.
Abstract: Widespread Miocene (24-8 Ma) ultrapotassic rocks and their entrained xenoliths provide information on the composition, structure, and thermal state of the sub-continental lithospheric mantle in southern Tibet during the India-Asia continental collision. The ultrapotassic rocks along the Lhasa block delineate two distinct lithospheric domains with different histories of depletion and enrichment. The eastern ultrapotassic rocks (89°E-92°E) reveal a depleted, young, and fertile lithospheric mantle (87Sr/86Srt = 0.704-0.707 [t is eruption time]; Hf depleted-mantle model age [TDM] = 377-653 Ma). The western ultrapotassic rocks (79°E-89°E) and their peridotite xenoliths (81°E) reflect a refractory harzburgitic mantle refertilized by ancient metasomatism (lavas: 87Sr/86Srt = 0.714-0.734; peridotites: 87Sr/86Srt = 0.709-0.716). These data integrated with seismic tomography suggest that upwelling asthenosphere was diverted away from the deep continental root beneath the western Lhasa block, but rose to shallower depths beneath a thinner lithosphere in the eastern part. Heating of the lithospheric mantle by the rising asthenosphere ultimately generated the ultrapotassic rocks with regionally distinct geochemical signatures reflecting the different nature of the lithospheric mantle.
Geostandards and Geoanalytical Research, in press available, 16p.
Australia
deposit - Mud Tank
Abstract: Zircon megacrysts from the Mud Tank carbonatite, Australia, are being used in many laboratories as a reference material for LA-ICP-MS U-Pb dating and trace element measurement, and LA-MC-ICP-MS determination of Hf isotopes. We summarise a database of > 10000 analyses of Mud Tank zircon (MTZ), collected from 2000 to 2018 during its use as a secondary reference material for simultaneous U-Pb and trace element analysis, and for Hf-isotope analysis. Trace element mass fractions are highest in dark red-brown stones and lowest in colourless and gem-quality ones. Individual unzoned grains can be chemically homogeneous, while significant variations in trace element mass fraction are associated with oscillatory zoning. Chondrite-normalised trace element patterns are essentially parallel over large mass fraction ranges. A Concordia age of 731.0 ± 0.2 Ma (2s, n = 2272) is taken as the age of crystallisation. Some grains show lower concordant to mildly discordant ages, probably reflecting minor Pb loss associated with cooling and the Alice Springs Orogeny (450-300 Ma). Our weighted mean 176Hf/177Hf is 0.282523 ± 10 (2s, n = 9350); the uncertainties on this ratio reflect some heterogeneity, mainly between grains. A few analyses suggest that colourless grains have generally lower 176Hf/177Hf. MTZ is a useful secondary reference material for U-Pb and Hf-isotope analysis, but individual grains need to be carefully selected using CL imaging and tested for homogeneity, and ideally should be standardised by solution analysis.
Abstract: The primordial crust on the Earth formed from the crystallization of the surface magma ocean during the Hadean. However, geological surveys have found no evidence of rocks dating back to more than 4 Ga on the Earth's surface, suggesting the Hadean crust was lost due to some processes. We investigated the subduction of one of the possible candidates for the primordial crust, anorthosite and KREEP crust similar to the Moon, which is also considered to have formed from the crystallization of the magma ocean. Similar to the present Earth, the subduction of primordial crust by subduction erosion is expected to be an effective way of eliminating primordial crust from the surface. In this study, the subduction rate of the primordial crust via subduction channels is evaluated by numerical simulations. The subduction channels are located between the subducting slab and the mantle wedge and are comprised of primordial crust materials supplied mainly by subduction erosion. We have found that primordial anorthosite and KREEP crust of up to ~50 km thick at the Earth's surface was able to be conveyed to the deep mantle within 0.1-2 Gy by that mechanism.
Physics and Chemistry of Minerals, in press available 9p.
Technology
Garnet morphology
Abstract: We present a systematic experimental study on the phase transition, lattice microstrain, and order-disorder of cations for garnets in the majorite-pyrope system. Polycrystalline gem-quality garnets were synthesized at high pressure and high temperature using a Kawai-type multi-anvil apparatus. A phase transition from a cubic to tetragonal structure is clearly observed for garnets with the majorite content of more than 74 mol % through X-ray diffraction (XRD) and Raman scattering studies. Microstrain of garnets, evaluated with the Williamson-Hall plot on XRD profiles, shows a nonlinear dependence of the garnet compositions. The variation of the XRD peak broadening suggests the lattice microstrain of these garnets may be associated with the local structural heterogeneities due to the substitution of different cations via the coupled substitution (Mg2+ + Si4+ = 2Al3+) in the garnet structure. The width variation of Raman scattering peaks indicates that cation disorder occurs in the garnet structure for intermediate compositions. It is found that intermediate garnets and end-members have a minimum of microstrain, while those between end-members and intermediate compositions possess a larger microstrain.
Abstract: The composition of the early Earth’s atmosphere is believed to result from significant magma outgassing during the Archaean eon. It has been widely debated whether the oxygen fugacity (fo2) of the Earth’s mantle has remained constant over the last ~3.8 Ga to levels where volatiles were mostly in their mobile form [1,2], or whether the mantle has experienced a gradual increase of its redox state [3]. Both hypotheses raise fundamental questions on the effect of composition of the early Earth’s accreting material, the origin and availability of primordial carbon in Earth’s interior, and the migration rate of CO2-rich magmas. In addition, the occurrence in nature of carbonatites (or silicate-carbonatitic rocks), diamonds and carbides indicate a dominant control of the mantle redox state on the volatile speciation over time and, maybe, on mechanisms of their formation, reaction and migration through the silicate mantle. A recent model has been developed that combines both experimental results on the fo2 of preserved carbonaceous chondrites at high pressure and thermodynamic predictions of the the temporal variation of the mantle redox state, with the CO2-bearing magmas that could form in the early asthenospheric mantle. Since any variation in melt composition is expected to cause significant changes in the physical properties (e.g., viscosity and density), the migration rate of these magmas has been determined using recent in situ viscosity data on CO2-rich melts with the falling sphere technique. Our results allow determining the composition of CO2- bearing magmas as function of the increasing mantle redox state over time, and the mechanisms and rate for exchange of carbon between mantle reservoirs.
Abstract: The thermoelastic parameters of Ca3Cr2Si3O12 uvarovite garnet were examined in situ at high pressure up to 13 GPa and high temperature up to 1100 K by synchrotron radiation energy-dispersive X-ray diffraction within a 6-6-type multi-anvil press apparatus. A least-square fitting of room T data to a third-order Birch-Murnaghan (BM3) EoS yielded K0 = 164.2 ± 0.7 GPa, V0 = 1735.9 ± 0.3 Å3 (K’0 fixed to 4.0). P-V-T data were fitted simultaneously by a modified HT-BM3 EoS, which gave the isothermal bulk modulus K0 = 163.6 ± 2.6 GPa, K’0 = 4.1 ± 0.5, its temperature derivative (?K0,T/?T)P = -0.014 ± 0.002 GPa K-1, and the thermal expansion coefficients a0 = 2.32 ± 0.13 ×10-5 K-1 and b0 = 2.13 ± 2.18 ×10-9 K-2 (K’0 fixed to 4.0). Our results showed that the Cr3+ enrichment in natural systems likely increases the density of ugrandite garnets, resulting in a substantial increase of mantle garnet densities in regions where Cr-rich spinel releases chromium through a metasomatic reaction.
Abstract: The thermoelastic parameters of Ca3Cr2Si3O12 uvarovite garnet were examined in situ at high pressure up to 13 GPa and high temperature up to 1100 K by synchrotron radiation energy-dispersive X-ray diffraction within a 6-6-type multi-anvil press apparatus. A least-square fitting of room T data to a third-order Birch-Murnaghan (BM3) EoS yielded K0 = 164.2 ± 0.7 GPa, V0 = 1735.9 ± 0.3 Å3 (K’0 fixed to 4.0). P-V-T data were fitted simultaneously by a modified HT-BM3 EoS, which gave the isothermal bulk modulus K0 = 163.6 ± 2.6 GPa, K’0 = 4.1 ± 0.5, its temperature derivative (?K0,T/?T)P = -0.014 ± 0.002 GPa K-1, and the thermal expansion coefficients a0 = 2.32 ± 0.13 ×10-5 K-1 and b0 = 2.13 ± 2.18 ×10-9 K-2 (K’0 fixed to 4.0). Our results showed that the Cr3+ enrichment in natural systems likely increases the density of ugrandite garnets, resulting in a substantial increase of mantle garnet densities in regions where Cr-rich spinel releases chromium through a metasomatic reaction.
Abstract: The effect of aluminum (Al) on the elasticity of majorite-pyrope garnets was investigated by means of ultrasonic interferometry measurements on well-fabricated polycrystalline specimens. Both velocities and elastic moduli increase almost linearly with increasing Al content within analytical uncertainty. No significant variation of the velocities and elastic moduli is observed across the tetragonal-to-cubic phase transition at majorite with the pyrope content up to 26 mol% along the majorite-pyrope system. The elasticity variation of majorite-pyrope garnets is largely dominated by the Al content, while the phase transition as a result of cation ordering/disordering of Mg and Si via substitution of Al on octahedral sites cannot significantly affect elastic properties. Seismic velocity variations of a garnet-bearing mantle transition zone are therefore dominated by garnet composition (e.g., Al, Fe, Ca, and Na) rather than the tetragonal-to-cubic phase transition because of cation ordering/disordering.
Abstract: Several interstellar environments produce 'anomalous microwave emission', with brightness-peaks at tens-of-gigahertz frequencies. The emission's origins are uncertain - rapidly-spinning nano-particles could emit electric-dipole radiation, but polycyclic aromatic hydrocarbons proposed as the carrier are now found not to correlate with Galactic signals. The difficulty is to identify co-spatial sources over long lines of sight. Here we identify anomalous microwave emission in three proto-planetary discs. These are the only known systems that host hydrogenated nano-diamonds, in contrast to very common detection of polycyclic aromatic hydrocarbons. Spectroscopy locates the nano-diamonds close to the host-stars, at physically-constrained temperatures. Developing disc models, we reproduce the emission with diamonds 0.75-1.1 nanometres in radius, holding less than or equal to 1-2 per cent of the carbon budget. The microwave-emission:stellar-luminosity ratios are approximately constant, allowing nano-diamonds to be ubiquitous but emitting below detection thresholds in many star-systems. This can unify the findings with similar-sized diamonds found within solar system meteorites. As nano-diamond spectral absorption is seen in interstellar sightlines, these particles are also a candidate for generating galaxy-scale anomalous microwave emission.
Abstract: Plate tectonics may have gotten a pretty early start in Earth’s history. Most estimates put the onset of when the large plates that make up the planet’s outer crust began shifting at around 3 billion years ago. But a new study in the Sept. 22 Science that analyzes titanium in continental rocks asserts that plate tectonics began 500 million years earlier. Nicolas Greber, now at the University of Geneva, and colleagues suggest that previous studies got it wrong because researchers relied on chemical analyses of silicon dioxide in shales, sedimentary rocks that bear the detritus of a variety of continental rocks. These rocks’ silicon dioxide composition can give researchers an idea of when continental rocks began to diverge in makeup from oceanic rocks as a result of plate tectonics.But weathering can wreak havoc on the chemical makeup of shales. To get around that problem, Greber’s team turned to a new tool: the ratios of two titanium isotopes, forms of the same element that have different masses. The proportion of titanium isotopes in the rocks is a useful stand-in for the difference in silicon dioxide concentration between continental and oceanic rocks, and isn’t so easily altered by weathering. Those data helped the team estimate that continental rocks — and therefore plate tectonics — were already going strong by 3.5 billion years ago.
Moscow University Geology Bulletin, Vol. 72, 5, pp. 299-304.
Mantle
perovskite
Abstract: Semi-empirical and quantum chemical studies of Al atom energy in CaSiO3 and MgSiO3 with the perovskite-type structure at pressures and temperatures of the Earth’s mantle are reported. The phase diagram for CaSiO3 is reproduced and refined. Probable mechanisms of Al incorporation in the structures studied are considered. According to the results of the calculations, Al is preferably incorporated into MgSiO3, rather than into CaSiO3. Evaluation of the isomorphic capacity of perovskite phases in relation to Al shows that the Al content in MgSiO3 may reach 2.4 mol % at 120 GPa and 2400 K. CaSiO3 cannot be a source of Al atoms in the Earth’s mantle.
Phase relationships of hydrous alkalic magmas at high pressures: production of nepheline hawaiitic to mugearitic liquids by amphibole dominated fractional
Hutchinson, D.R., Lee, M.W., Behrendt, J., Cannon, W.F., Green
Variations in the reflectivity of the Moho transition zone beneath The midcontinent Rift System of North America. Results from true amplitude Glimpcedata
Journal of Geophysical Research, Vol. 97, No. B4, April 10, pp. 4721-4738
Chemical Reviews, Vol. 120, 4, 10.1021/ acs.chemrev.9b00578 50p. Pdf
Global
HPHT, CVD, synthetics
Abstract: Nitrogen is ubiquitous in both natural and laboratory-grown diamond, but the number and nature of the nitrogen-containing defects can have a profound effect on the diamond material and its properties. An ever-growing fraction of the supply of diamond appearing on the world market is now lab-grown. Here, we survey recent progress in two complementary diamond synthesis methods: high pressure high temperature (HPHT) growth and chemical vapor deposition (CVD), how each is allowing ever more precise control of nitrogen incorporation in the resulting diamond, and how the diamond produced by either method can be further processed (e.g., by implantation or annealing) to achieve a particular outcome or property. The burgeoning availability of diamond samples grown under well-defined conditions has also enabled huge advances in the characterization and understanding of nitrogen-containing defects in diamond alone and in association with vacancies, hydrogen, and transition metal atoms. Among these, the negatively charged nitrogen-vacancy (NV-) defect in diamond is attracting particular current interest in account of the many new and exciting opportunities it offers for, for example, quantum technologies, nanoscale magnetometry, and biosensing.
Abstract: Large (> 100 mm3), relatively pure (type II) and low birefringence single crystal diamond can be produced by high pressure high temperature (HPHT) synthesis. In this study we examine a HPHT sample of good crystalline perfection, containing less than 1 ppb (part per billion carbon atoms) of boron impurity atoms in the {001} growth sector and only tens of ppb of nitrogen impurity atoms. It is shown that the boundaries between {111} and {113} growth sectors are decorated by negatively charged nitrogen vacancy centres (NV-): no decoration is observed at any other type of growth sector interface. This decoration can be used to calculated the relative {111} and {113} growth rates. The bulk (001) sector contains concentrations of luminescent point defects (excited with 488 and 532 nm wavelengths) below 1011 cm-3 (10-3 ppb). We observe the negatively charged silicon-vacancy (SiV-) defect in the bulk {111} sectors along with a zero phonon line emission associated with a nickel defect at 884 nm (1.40 eV). No preferential orientation is seen for either NV- or SiV- defects, but the nickel related defect is oriented with its trigonal axis along the <111> sector growth direction. Since the NV- defect is expected to readily re-orientate at HPHT diamond growth temperatures, no preferential orientation is expected for this defect but the lack of preferential orientation of SiV- in {111} sectors is not explained.
Gems & Gemology, Sixth International Gemological Symposium Vol. 54, 3, 1p. Abstract p. 266.
Global
Fluoresence
Abstract: Photoluminescence (PL) and phosphorescence underpin many of the discrimination techniques used to separate natural from synthetic diamond. PL is at the heart of many new quantum technologies based on color centers in lab-grown diamonds. In HPHT synthetic diamond, the phosphorescence observed is explained in terms of donor-acceptor pair recombination. The thermal activation of electrons to neutral boron acceptors shows that boron plays a key role in the phosphorescence process. However, there are a number of things we struggle to explain. For example, the phosphorescence peak positions are not fully explained, and there is no conclusive link between the emission and charge transfer involving the substitutional nitrogen donor. Secondly, the origin of the phosphorescence observed in some synthetic diamond samples grown by the CVD process is unclear. Although we now have evidence for unintentional boron impurity incorporation at stop-start growth boundaries in some CVD syn- thetic samples, it is possible that some of the observed phosphorescence does not involve boron impurities. In this paper we report on the results of combined fluorescence, phosphorescence, thermoluminescence, and quantitative charge transfer investigations undertaken on both HPHT and CVD synthetic diamond, with the objective of identifying which defects are involved in the fluorescence and phosphorescence processes.
Geochemistry: Exploration, Environment, Analysis, Vol. 19, pp. 414-430.
Canada, British Columbia
geochemistry
Abstract: Using Rock Canyon Creek REE-F-Ba deposit as an example, we demonstrate the need for verifying inherited geochemical data. Inherited La, Ce, Nd, and Sm data obtained by pressed pellet XRF, and La and Y data obtained by aqua regia digestion ICP-AES for 300 drill-core samples analysed in 2009 were compared to sample subsets reanalysed using lithium metaborate-tetraborate (LMB) fusion ICP-MS, Na2O2 fusion ICP-MS, and LMB fusion-XRF. We determine that LMB ICP-MS and Na2O2 ICP-MS accurately determined REE concentrations in SY-2 and SY-4, and provided precision within 10%. Fusion-XRF was precise for La and Nd at concentrations exceeding ten times the lower detection limit; however, accuracy was not established because REE concentrations in SY-4 were below the lower detection limit. Analysis of the sample subset revealed substantial discrepancies for Ce concentrations determined by pressed pellet XRF in comparison to other methods due to Ba interference. Samarium, present in lower concentrations than other REE compared, was underestimated by XRF methods relative to ICP-MS methods. This may be due to Sm concentrations approaching the lower detection limits of XRF methods, elemental interference, or inadequate background corrections. Aqua regia dissolution ICP-AES results, reporting for La and Y, are underestimated relative to other methods.
Abstract: Several interstellar environments produce 'anomalous microwave emission', with brightness-peaks at tens-of-gigahertz frequencies. The emission's origins are uncertain - rapidly-spinning nano-particles could emit electric-dipole radiation, but polycyclic aromatic hydrocarbons proposed as the carrier are now found not to correlate with Galactic signals. The difficulty is to identify co-spatial sources over long lines of sight. Here we identify anomalous microwave emission in three proto-planetary discs. These are the only known systems that host hydrogenated nano-diamonds, in contrast to very common detection of polycyclic aromatic hydrocarbons. Spectroscopy locates the nano-diamonds close to the host-stars, at physically-constrained temperatures. Developing disc models, we reproduce the emission with diamonds 0.75-1.1 nanometres in radius, holding less than or equal to 1-2 per cent of the carbon budget. The microwave-emission:stellar-luminosity ratios are approximately constant, allowing nano-diamonds to be ubiquitous but emitting below detection thresholds in many star-systems. This can unify the findings with similar-sized diamonds found within solar system meteorites. As nano-diamond spectral absorption is seen in interstellar sightlines, these particles are also a candidate for generating galaxy-scale anomalous microwave emission.
Coexisting Garnets and Ilmenites Synthesized at High Pressure pressures from Pyrolite and Olivine Basanite and Their Significance for Kimberlitic Assemblages.
Contributions to Mineralogy and Petrology, Vol. 50, PP. 217-229.
Ultramafic Xenoliths from Lake Bulletinen Merri and Mt. Leura, South East Australia, and Their Bearing on the Evolution of The Continental Upper Mantle.
Proceedings of Third International Kimberlite Conference, TERRA COGNITA, ABSTRACT VOLUME., Vol. 2, No. 3, P. 230, (abstract.).
high pressure experimental calibration of the olivine ortho pyroxene spinel oxygen geobarometer-implications for the oxidation state of the upper mantle
Contributions to Mineralogy and Petrology, Vol. 107, No. 1, pp. 27-40
Mineral chem. of silicate and oxide phases from fertile peridotite equilibrated with a C-O-H fluid phase- a low fO2 dat a set- evaluation of mineralbarometers, therM.
Proceedings of Fifth International Kimberlite Conference held Araxa June 1991, Servico Geologico do Brasil (CPRM) Special, pp. 417-419
Tian, W., Chen, B., Ireland, T.R., Green, D.H., Suzuki, K., Chu, Z.
Petrology and geochemistry of dunites, chromitites and mineral inclusions from the Gaositai Alaskan type complex, North Chin a craton: mantle source characters
Physics and Chemistry of Minerals, Vol. 42, 2, pp. 95-122.
Mantle
Peridotite
Abstract: For over 50 years, the use of high-pressure piston/cylinder apparatus combined with an increasing diversity of microbeam analytical techniques has enabled the study of mantle peridotite compositions and of magmas derived by melting in the upper mantle. The experimental studies have been guided by the petrology and geochemistry of peridotites from diverse settings and by the remarkable range of mantle-derived magma types. Recent experimental study using FTIR spectroscopy to monitor water content of minerals has shown that fertile lherzolite (MORB-source upper mantle) at ~1,000 °C can store ~200 ppm H2O in defect sites in nominally anhydrous minerals (olivine, pyroxenes, garnet and spinel). Water in excess of 200 ppm stabilizes amphibole (pargasite) at P < 3 GPa up to the lherzolite solidus. However, at P > 3 GPa, water in excess of 200 ppm appears as an aqueous vapour phase and this depresses the temperature of the upper mantle solidus. Provided the uppermost mantle (lithosphere) has H2O < 4,000 ppm, the mantle solidus has a distinctive P, T shape. The temperature of the vapour-undersaturated or dehydration solidus is approximately constant at 1,100 °C at pressures up to ~3 GPa and then decreases sharply to ~1,010 °C. The strongly negative dT/dP of the vapour-undersaturated solidus of fertile lherzolite from 2.8 to 3 GPa provides the basis for understanding the lithosphere/asthenosphere boundary. Through upward migration of near-solidus hydrous silicate melt, the asthenosphere becomes geochemically zoned with the ‘enriched’ intraplate basalt source (>500 ppm H2O) overlying the ‘depleted’ MORB source (~200 ppm H2O). From the study of primitive MOR picrites, the modern mantle potential temperature for MORB petrogenesis is ~1,430 °C. The intersection of the 1,430 °C adiabat with the vapour-saturated lherzolite solidus at ~230 km suggests that upwelling beneath mid-ocean ridges begins around this depth. In intraplate volcanism, diapiric upwelling begins from shallower depths and lower temperatures within the asthenosphere and the upwelling lherzolite is enriched in water, carbonate and incompatible elements. Magmas including olivine melilitites, olivine nephelinites, basanites, alkali picrites and tholeiitic picrites are consequences of increasing melt fraction and decreasing pressure at melt segregation. Major element, trace element and isotopic characteristics of island chain or ‘hot-spot’ magmas show that they sample geochemically distinct components in the upper mantle, differing from MORB sources. There is no evidence for higher-temperature ‘hot-spot’ magmas, relative to primitive MORB, but there is evidence for higher water, CO2 and incompatible element contents. The distinctive geochemical signatures of ‘hot-spot’ magmas and their ‘fixed’ position and long-lived activity relative to plate movement are attributed to melt components derived from melting at interfaces between old, oxidised subducted slabs (suspended beneath or within the deeper asthenosphere) and ambient, reduced mantle. In convergent margin volcanism, the inverted temperature gradients inferred for the mantle wedge above the subducting lithosphere introduce further complexity which can be explored by overlaying the phase relations of appropriate mantle and crustal lithologies. Water and carbonate derived from the subducted slab play significant roles, magmas are relatively oxidised, and distinctive primary magmas such as boninites, adakites and island arc ankaramites provide evidence for fluxing of melting in refractory harzburgite to lherzolite by slab-derived hydrous adakitic melt and by wedge-derived carbonatite.
Physics and Chemistry of Minerals, Vol. 42, pp. 95-102.
Mantle
Peridotite
Abstract: For over 50 years, the use of high-pressure piston/cylinder apparatus combined with an increasing diversity of microbeam analytical techniques has enabled the study of mantle peridotite compositions and of magmas derived by melting in the upper mantle. The experimental studies have been guided by the petrology and geochemistry of peridotites from diverse settings and by the remarkable range of mantle-derived magma types. Recent experimental study using FTIR spectroscopy to monitor water content of minerals has shown that fertile lherzolite (MORB-source upper mantle) at ~1,000 °C can store ~200 ppm H2O in defect sites in nominally anhydrous minerals (olivine, pyroxenes, garnet and spinel). Water in excess of 200 ppm stabilizes amphibole (pargasite) at P < 3 GPa up to the lherzolite solidus. However, at P > 3 GPa, water in excess of 200 ppm appears as an aqueous vapour phase and this depresses the temperature of the upper mantle solidus. Provided the uppermost mantle (lithosphere) has H2O < 4,000 ppm, the mantle solidus has a distinctive P, T shape. The temperature of the vapour-undersaturated or dehydration solidus is approximately constant at 1,100 °C at pressures up to ~3 GPa and then decreases sharply to ~1,010 °C. The strongly negative dT/dP of the vapour-undersaturated solidus of fertile lherzolite from 2.8 to 3 GPa provides the basis for understanding the lithosphere/asthenosphere boundary. Through upward migration of near-solidus hydrous silicate melt, the asthenosphere becomes geochemically zoned with the ‘enriched’ intraplate basalt source (>500 ppm H2O) overlying the ‘depleted’ MORB source (~200 ppm H2O). From the study of primitive MOR picrites, the modern mantle potential temperature for MORB petrogenesis is ~1,430 °C. The intersection of the 1,430 °C adiabat with the vapour-saturated lherzolite solidus at ~230 km suggests that upwelling beneath mid-ocean ridges begins around this depth. In intraplate volcanism, diapiric upwelling begins from shallower depths and lower temperatures within the asthenosphere and the upwelling lherzolite is enriched in water, carbonate and incompatible elements. Magmas including olivine melilitites, olivine nephelinites, basanites, alkali picrites and tholeiitic picrites are consequences of increasing melt fraction and decreasing pressure at melt segregation. Major element, trace element and isotopic characteristics of island chain or ‘hot-spot’ magmas show that they sample geochemically distinct components in the upper mantle, differing from MORB sources. There is no evidence for higher-temperature ‘hot-spot’ magmas, relative to primitive MORB, but there is evidence for higher water, CO2 and incompatible element contents. The distinctive geochemical signatures of ‘hot-spot’ magmas and their ‘fixed’ position and long-lived activity relative to plate movement are attributed to melt components derived from melting at interfaces between old, oxidised subducted slabs (suspended beneath or within the deeper asthenosphere) and ambient, reduced mantle. In convergent margin volcanism, the inverted temperature gradients inferred for the mantle wedge above the subducting lithosphere introduce further complexity which can be explored by overlaying the phase relations of appropriate mantle and crustal lithologies. Water and carbonate derived from the subducted slab play significant roles, magmas are relatively oxidised, and distinctive primary magmas such as boninites, adakites and island arc ankaramites provide evidence for fluxing of melting in refractory harzburgite to lherzolite by slab-derived hydrous adakitic melt and by wedge-derived carbonatite.
Abstract: Primary or parental magmas act as probes to infer eruption and source temperatures for both mid-ocean ridge (MOR) and ‘hot-spot’ magmas (tholeiitic picrites). The experimental petrogenetic constraints (‘inverse’ experiments) argue for no significant temperature differences between them. However, there are differences in major, minor and trace elements which characterise geochemical, not thermal, anomalies beneath ‘hot-spots’. We suggest that diapiric upwelling from interfaces (redox contrasts) between old subducted slab and normal MOR basalt source mantle is the major reason for the observed characteristics of island chain or ‘hot-spot’ volcanism. Intraplate basalts also include widely distributed volcanic centres containing lherzolite xenoliths, i.e. mantle-derived magmas. Inverse experiments on olivine basalt, alkali olivine basalt, olivine basanite, olivine nephelinite, olivine melilitite and olivine leucitite (lamproite) determined liquidus phases as a function of pressure, initially under anhydrous and CO2-absent conditions. Under C- and H-absent conditions, only tholeiites to alkali olivine basalts had Ol + Opx ± Cpx as high-pressure liquidus phases. Addition of H2O accessed olivine basanites at 2.5-3 GPa, ~1,200 °C, but both CO2 and H2O were necessary to obtain saturation with Ol, Opx, Cpx and Ga at 2.5-3.5 GPa for olivine nephelinite and olivine melilitite. The forward and inverse experimental studies are combined to formulate a petrogenetic grid for intraplate, ‘hot-spot’ and MOR magmatism within the plate tectonics paradigm. The asthenosphere is geochemically zoned by slow upward migration of incipient melt. The solidus and phase stabilities of lherzolite with very small water contents (<3,000 ppm) determine the thin plate behaviour of the oceanic lithosphere and thus the Earth’s convection in the form of plate tectonics. There is no evidence from the parental magmas of MOR and ‘hot-spots’ to support the ‘deep mantle thermal plume’ hypothesis. The preferred alternative is the presence of old subducted slabs, relatively buoyant and oxidised with respect to MORB source mantle and suspended or upwelling in or below the lower asthenosphere (and thus detached from overlying plate movement).
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.
Trace element partitioning between mica and amphibole bearing garnet lherzolite and hydrous basanitic melt: 1. experimental results and the investigation controls
Contributions to Mineralogy and Petrology, Online, available
Adam, J., Oberti, R., Camara, F., Green, T.H., Rushmer, T.
The effect of water on equilibrium relations between clinopyroxenes and basanitic magmas: tracing water and non- volatile incompatible elements in the Earth's mantle.
Dorfman, S.M., Potapkin, V., Lv, M., Greenberg, E., Kupenko, I., Chumakov, A.I., Bi, W., Alp, E.E., Liu, J., Magrez, A., Dutton, S.E., Cava, R.J., McCammon, C.A., Gillet, P.
American Mineralogist, Vol. 105, pp. 1030-1039. pdf
Mantle
redox
Abstract:
Electronic states of iron in the lower mantle's dominant mineral, (Mg,Fe,Al)(Fe,Al,Si)O3 bridgmanite, control physical properties of the mantle including density, elasticity, and electrical and thermal conductivity. However, the determination of electronic states of iron has been controversial, in part due to different interpretations of Mössbauer spectroscopy results used to identify spin state, valence state, and site occupancy of iron. We applied energy-domain Mössbauer spectroscopy to a set of four bridgmanite samples spanning a wide range of compositions: 10-50% Fe/total cations, 0-25% Al/total cations, 12-100% Fe3+/total Fe. Measurements performed in the diamond-anvil cell at pressures up to 76 GPa below and above the high to low spin transition in Fe3+ provide a Mössbauer reference library for bridgmanite and demonstrate the effects of pressure and composition on electronic states of iron. Results indicate that although the spin transition in Fe3+ in the bridgmanite B-site occurs as predicted, it does not strongly affect the observed quadrupole splitting of 1.4 mm/s, and only decreases center shift for this site to 0 mm/s at ~70 GPa. Thus center shift can easily distinguish Fe3+ from Fe2+ at high pressure, which exhibits two distinct Mössbauer sites with center shift ~1 mm/s and quadrupole splitting 2.4-3.1 and 3.9 mm/s at ~70 GPa. Correct quantification of Fe3+/total Fe in bridgmanite is required to constrain the effects of composition and redox states in experimental measurements of seismic properties of bridgmanite. In Fe-rich, mixed-valence bridgmanite at deep-mantle-relevant pressures, up to ~20% of the Fe may be a Fe2.5+ charge transfer component, which should enhance electrical and thermal conductivity in Fe-rich heterogeneities at the base of Earth's mantle.
Abstract: Diamonds are the deepest accessible “fragments” of Earth, providing records of deep geological processes. Absolute ages for diamond formation are crucial to place these records in the correct time context. Diamond ages are typically determined by dating inclusions, assuming that they were formed simultaneously with their hosts. One of the most widely used mineral inclusions for dating diamond is garnet, which is amenable to Sm-Nd geochronology and is common in lithospheric diamonds. By investigating worldwide garnet-bearing diamonds, we provide crystallographic evidence that garnet inclusions that were previously considered to be syngenetic may instead be protogenetic, i.e., they were formed before the host diamond, raising doubts about the real significance of many reported diamond “ages.” Diffusion modeling at relevant pressures and temperatures, however, demonstrates that isotopic resetting would generally occur over geologically short time scales. Therefore, despite protogenicity, the majority of garnet-based ages should effectively correspond to the time of diamond formation. On the other hand, our results indicate that use of large garnet inclusions (e.g., >100 µm) and diamond hosts formed at temperatures lower than ~1000 °C is not recommended for diamond age determinations.
Abstract: Wehrlite and pyroxenite xenoliths and megacrysts from the Jericho kimberlite were analyzed by µXRF and EBSD, and for major elements, trace elements, and isotopes (Pb-Sr- O) in major phases. Thermobarometry places these samples at 60 - 180 km and 600 - 1200 ??C. While modes and textures vary, many samples have olivine-olivine grain boundaries with straight edges and 120° angle junctions, indicating granoblastic recrystallisation, while clinopyroxene and orthopyroxene are complexly intergrown. Clinopyroxene twins and subgrains recording orientations distinct from the encapsulating grain were detected using EBSD and are inferred to represent recent modification processes. Several distinct garnet compositions were measured, with multiple thin garnet rims in some samples suggesting possible successive stages of garnet crystallisation. Complex chromium zoning in garnet is detected by µXRF in several samples (fig.1). Pb-Pb ages for most samples are similar to the age of kimberlite entrainment (173 Ma), but the shallowest pyroxenite sample preserves the most radiogenic Pb composition, intercecting concordia at 0.7 - 1.1 Ga, and is the only sample with d18O above the mantle range (6.2±0.1 ‰). The deepest sample has the lowest d18O (5.5±0.1 ‰) and radiogenic 87Sr/86Sr similar to MARID rocks (0.709±1 ‰). These results suggest the Jericho lithosphere experienced several melt/fluid injection events that modified substantial portions of the sampled section soon before kimberlite entrainment.
International Journal of Earth Sciences, Vol. 107, 3, pp. 787-810.
Mantle
geochemistry
Abstract: Archean and Proterozoic subcontinental lithospheric mantle (SLM) is compared using 83 similarly incompatible element ratios (SIER; minimally affected by % melting or differentiation, e.g., Rb/Ba, Nb/Pb, Ti/Y) for >3700 basalts from ten continental flood basalt (CFB) provinces representing nine large igneous provinces (LIPs). Nine transition metals (TM; Fe, Mn, Sc, V, Cr, Co, Ni, Cu, Zn) in 102 primitive basalts (Mg# = 0.69-0.72) from nine provinces yield additional SLM information. An iterative evaluation of SIER values indicates that, regardless of age, CFB transecting Archean lithosphere are enriched in Rb, K, Pb, Th and heavy REE(?); whereas P, Ti, Nb, Ta and light REE(?) are higher in Proterozoic-and-younger SLM sources. This suggests efficient transfer of alkali metals and Pb to the continental lithosphere perhaps in association with melting of subducted ocean floor to form Archean tonalite-trondhjemite-granodiorite terranes. Titanium, Nb and Ta were not efficiently transferred, perhaps due to the stabilization of oxide phases (e.g., rutile or ilmenite) in down-going Archean slabs. CFB transecting Archean lithosphere have EM1-like SIER that are more extreme than seen in oceanic island basalts (OIB) suggesting an Archean SLM origin for OIB-enriched mantle 1 (EM1). In contrast, OIB high U/Pb (HIMU) sources have more extreme SIER than seen in CFB provinces. HIMU may represent subduction-processed ocean floor recycled directly to the convecting mantle, but to avoid convective homogenization and produce its unique Pb isotopic signature may require long-term isolation and incubation in SLM. Based on all TM, CFB transecting Proterozoic lithosphere are distinct from those cutting Archean lithosphere. There is a tendency for lower Sc, Cr, Ni and Cu, and higher Zn, in the sources for Archean-cutting CFB and EM1 OIB, than Proterozoic-cutting CFB and HIMU OIB. All CFB have SiO2 (pressure proxy)-Nb/Y (% melting proxy) relationships supporting low pressure, high % melting resembling OIB tholeiites, but TM concentrations do not correlate with % melting. Thus, the association of layered intrusion (plutonic CFB) TM deposits with Archean terranes does not appear related to higher metal concentrations or higher percentages of melting in Archean SLM. Other characteristics of these EM1-like magmas (e.g., S2 or O2 fugacity) may lead to element scavenging and concentration during differentiation to form ore deposits.
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.
Oxygen isotope evidence for the origin of pyroxenites in the Beni Bousera peridotite massif, North Morocco: derivation from subducted oceaniclithosphere
Earth and Planetary Science Letters, Vol. 102, No. 3/4, March pp. 289-301
Earth and Planetary Science Letters, Vol. 453, pp. 146-156.
Canada, Ontario
Gravity
Abstract: The Earth's surface was depressed under the weight of ice during the last glaciations. Glacial Isostatic Adjustment (GIA) induces the slow recession of the trough that is left after deglaciation and is responsible for a contemporary uplift rate of more than 1 cm/yr around Hudson Bay. The present-day residual depression, an indicator of still-ongoing GIA, is difficult to identify in the observed topography, which is predominantly sensitive to crustal heterogeneities. According to the most widespread GIA models, which feature a viscosity of on top of the lower mantle, the trough is approximately 100 m deep and cannot explain the observed gravity anomalies across North America. These large anomalies are therefore usually attributed to subcontinental density heterogeneities in the tectosphere or to slab downwelling in the deep mantle.
Earth Planetary Science Letters, Vol. 487, pp. 210-220.
Africa
tectonics
Abstract: Rifts are often associated with ancient traces of hotspots, which are supposed to participate to the weakening of the lithosphere. We investigated the expected past trajectories followed by three hotspots (Afar, East-Africa and Lake-Victoria) located around the Red Sea. We used a hotspot reference frame to compute their location with respect to time, which is then compared to mantle tomography interpretations and geological features. Their tracks are frequently situated under continental crust, which is known to strongly filter plume activity. We looked for surface markers of their putative ancient existence, such as volcanism typology, doming, and heat-flow data from petroleum wells. Surface activity of the East-Africa hotspot is supported at 110 Ma, 90 Ma and 30 Ma by uplift, volcanic activity and rare gas isotopic signatures, reminiscent of a deep plume origin. The analysis of heat-flow data from petroleum wells under the Arabian plate shows a thermal anomaly that may correspond to the past impact of the Afar hotspot. According to derived hotspot trajectories, the Afar hotspot, situated (at 32 Ma) 1000 km north-east of the Ethiopian-Yemen traps, was probably too far away to be accountable for them. The trigger of the flood basalts would likely be linked to the East-Africa hotspot. The Lake-Victoria hotspot activity appears to have been more recent, attested only by Cenozoic volcanism in an uplifted area. Structural and thermal weakening of the lithosphere may have played a major role in the location of the rift systems. The Gulf of Aden is located on inherited Mesozoic extensional basins between two weak zones, the extremity of the Carlsberg Ridge and the present Afar triangle, previously impacted by the East-Africa hotspot. The Red Sea may have opened in the context of extension linked to Neo-Tethys slab-pull, along the track followed by the East Africa hotspot, suggesting an inherited thermal weakening.
The Tornquist Zone, north east inclining lithospheric transition at the south western margin of the Baltic Shield: revealed through a nonlinear teleseismic tomographic inversion.
Tectonophysics, Vol. 416, 1-4, April 5, pp. 151-166.
Enigmatic relationship between silicic and volcanic and plutonic rocks: geophysical evidence for silicic crustal melt in the continents: where. What kind, and how much?
Gregoire, M., Tinguely, C., Bell, D.R., Le Roex, A.P.
Spinel lherzolite xenoliths from the Premier kimberlite ( Kaapvaal craton) South Africa: nature and evolution of the shallow upper mantle beneath Bushveld Complex.
On the iron isotope heterogeneity of lithospheric mantle xenoliths: implications for mantle metasomatism, the origin of basalts and the iron isotope composition of the Earth.
Contributions to Mineralogy and Petrology, Vol. 165, 6, pp. 1243-1258.
Abstract: Pyroxenites and garnet pyroxenites are mantle heterogeneities characterized by a lower solidus temperature than the enclosing peridotites; it follows that they are preferentially involved during magma genesis. Constraining their origin, composition, and the interactions they underwent during their subsequent evolution is therefore essential to discuss the sources of magmatism in a given area. Pyroxenites could represent either recycling of crustal rocks in mantle domains or mantle originated rocks (formed either by olivine consuming melt-rock reactions or by crystal fractionation). Petrological and geochemical (major and trace elements, Sr-Nd and O isotopes) features of xenoliths from various occurrences (French Massif-Central, Jordan, Morocco and Cameroon) show that these samples represent cumulates crystallized during melt percolation at mantle conditions. They formed in mantle domains at pressures of 1-2 GPa during post-collisional magmatism (possibly Hercynian for the French Massif-Central, and Panafrican for Morocco, Jordan and Cameroon). The thermal re-equilibration of lithospheric domains, typical of the late orogenic exhumation stages, is also recorded by the samples. Most of the samples display a metasomatic overprint that may be either inherited or likely linked to the recent volcanic activity that occurred in the investigated regions. The crystallization of pyroxenites during late orogenic events has implications for the subsequent evolution of the mantle domains. The presence of large amounts of mantle pyroxenites in old orogenic regions indeed imparts peculiar physical and chemical characteristics to these domains. Among others, the global solidus temperature of the whole lithospheric domain will be lowered; in turn, this implies that old orogenic regions are refertilized zones where magmatic activity would be enhanced.
Abstract: It is now accepted that significant volumes of pyroxenites are generated in the subduction factory and remain trapped in the mantle. In ophiolites and orogenic massifs the geometry of pyroxenite layers and their relationships with the host peridotite can be observed directly. Since a large part of what is known about the upper mantle structure is derived from the analysis of seismic waves, it is crucial to integrate pyroxenites in the interpretations. We modeled the seismic properties of a peridotitic mantle rich in pyroxenite layers in order to determine the impact of layering on the seimsic properties. To do so, EBSD data on deformed and undeformed pyroxenites from the Cabo Ortegal complex (Spain) and the Trinity ophiolite (California, USA) respectively are combined with either A or B-type olivine fabrics in order to model a realistic pyroxenite-rich upper mantle. Consideration of pyroxeniterich domains within the host mantle wall rock is incorporated in the calculations using the Schoenberg and Muir group theory [1]. This quantification reveals the complex dependence of the seismic signal on the deformational state and relative abundance of each mineral phase. The incorporation of pyroxenites properties into geophysical interpretations in understanding the lithospheric structure of subduction zones will lead to more geologically realistic models.
Abstract: Mantle lithologies in orogenic massifs and xenoliths commonly display strikingly different Hf- and Nd-isotope compositions compared to oceanic basalts. While the presence of pyroxenites has long been suggested in the source region of mantle-derived magmas, very few studies have reported their combined HfNd isotope compositions. We here report the first LuHf data along with ReOs data and S concentrations on the Cabo Ortegal Complex, where the pyroxenite-rich Herbeira massif has been interpreted as remnants of a delaminated arc root. The pyroxenites, chromitites and their host harzburgites show a wide range of whole-rock 187Re/188Os and 187Os/188Os (0.16-1.44), indicating that Re was strongly mobilized, partly during hydrous retrograde metamorphism but mostly during supergene alteration that preferentially affected low-Mg#, low Cu/S pyroxenites. Samples that escaped this disturbance yield an isochron age of 838 ± 42 Ma, interpreted as the formation of Cabo Ortegal pyroxenites. Corresponding values of initial 187Os/188Os (0.111-0.117) are relatively unradiogenic, suggesting limited contributions of slab-derived Os to primitive arc melts such as those parental to these pyroxenites. This interpretation is consistent with radiogenic Os in arc lavas being mostly related to crustal assimilation. Paleoproterozoic to Archean Os model ages confirm that Cabo Ortegal pyroxenites record incipient volcanic arc magmatism on the continental margin of the Western African Craton, as notably documented by zircon UPb ages of 2.1 and 2.7 Ga. LuHf data collected on clinopyroxene and amphibole separates and whole-rock samples are characterized by uncorrelated 176Lu/177Hf and 176Hf/177Hf (0.2822-0.2855), decoupled from Nd-isotope compositions. This decoupling is ascribed to diffusional disequilibrium during melt-peridotite interaction, in good agreement with the results of percolation-diffusion models simulating the interaction of an arc melt with an ancient melt-depleted residue. These models notably show that HfNd isotopic decoupling such as recorded by Cabo Ortegal pyroxenites and peridotites (??Hf(i) up to +97) is enhanced during melt-peridotite interaction by slow diffusional re-equilibration and can be relatively insensitive to chromatographic fractionation. Finally, we discuss the hypothesis that arc-continent interaction may provide preferential conditions for such isotopic decoupling and propose that its ubiquitous recognition in peridotites reflects the recycling of sub-arc mantle domains derived from ancient, reworked SCLM.
Journal of Petrology, https://doi.org/ 10.1093/petrology /egaa040 50p. Pdf
Africa, South Africa
kimberlites
Abstract: Eclogite xenoliths, together with garnet pyroxenites and some mafic garnet granulites, found in kimberlites located along the southern margin of the Kaapvaal craton in southern Africa have been analysed by electron microprobe and mass spectrometry techniques to determine their geochemical characteristics. The majority of eclogites are bimineralic with garnet and omphacitic clinopyroxene in subequal proportions, with rutile as the main accessory phase; a few contain kyanite. Based on K2O in clinopyroxene and Na2O in garnet, the eclogites can be classified as Group II eclogites, and the majority are high-Ca in character. Garnet pyroxenites comprise garnet clinopyroxenites and garnet websterites. Major and trace element concentrations and isotope ratios of reconstituted bulk rock compositions of the eclogites and garnet pyroxenites allow constraints to be placed on depth of origin and likely protolith history. Calculated Fe–Mg exchange equilibration temperatures for the eclogites range from 815 to 1000?°C, at pressures of 1·7?±?0·4?GPa as determined by REE partitioning, indicating that they were sampled from depths of 50–55?km; i.e. within the lower crust of the Namaqua–Natal Belt. The garnet pyroxenites show slightly lower temperatures (686–835?°C) at similar pressures of equilibration. Initial 143Nd/144Nd and 87Sr/86Sr ratios (calculated to time of kimberlite emplacement) of both lithologies overlap the field for lower crustal samples from the Namaqua–Natal Belt. Further evidence for a crustal origin is found in the similar REE patterns shown by many of the associated garnet granulite xenoliths. Garnet pyroxenites are interpreted to have a similar origin as the associated eclogites but with the mafic protolith having insufficient Na (i.e. low modal plagioclase) to allow for development of omphacitic pyroxene. Metamorphism of the mafic protoliths to these eclogites and garnet pyroxenites is inferred to have occurred during crustal shortening and thickening associated with the collision of the Namaqua–Natal Belt with the Kaapvaal craton at 1–1·2?Ga.
Abstract: Eclogite xenoliths, together with garnet pyroxenites and some mafic garnet granulites, found in kimberlites located along the southern margin of the Kaapvaal craton in southern Africa have been analysed by electron microprobe and mass spectrometry techniques to determine their geochemical characteristics. The majority of eclogites are bimineralic with garnet and omphacitic clinopyroxene in subequal proportions, with rutile as the main accessory phase; a few contain kyanite. Based on K2O in clinopyroxene and Na2O in garnet, the eclogites can be classified as Group II eclogites, and the majority are high-Ca in character. Garnet pyroxenites comprise garnet clinopyroxenites and garnet websterites. Major and trace element concentrations and isotope ratios of reconstituted bulk rock compositions of the eclogites and garnet pyroxenites allow constraints to be placed on depth of origin and likely protolith history. Calculated Fe-Mg exchange equilibration temperatures for the eclogites range from 815 to 1000?°C, at pressures of 1•7?±?0•4?GPa as determined by REE partitioning, indicating that they were sampled from depths of 50-55?km; i.e. within the lower crust of the Namaqua-Natal Belt. The garnet pyroxenites show slightly lower temperatures (686-835?°C) at similar pressures of equilibration. Initial 143Nd/144Nd and 87Sr/86Sr ratios (calculated to time of kimberlite emplacement) of both lithologies overlap the field for lower crustal samples from the Namaqua-Natal Belt. Further evidence for a crustal origin is found in the similar REE patterns shown by many of the associated garnet granulite xenoliths. Garnet pyroxenites are interpreted to have a similar origin as the associated eclogites but with the mafic protolith having insufficient Na (i.e. low modal plagioclase) to allow for development of omphacitic pyroxene. Metamorphism of the mafic protoliths to these eclogites and garnet pyroxenites is inferred to have occurred during crustal shortening and thickening associated with the collision of the Namaqua-Natal Belt with the Kaapvaal craton at 1-1•2?Ga.
Abstract: Carbonatites are carbonate-dominated igneous rocks derived by low-degree partial melting of metasomatized mantle, although the geodynamic processes responsible for their emplacement into the crust are disputed. Current models favor either reactivation of lithospheric structures in response to plate movements, or the impingement of mantle plumes. Geochronology provides a means of testing these models, but constraining the age of carbonatites and related metasomatic events is rarely straightforward. We use in situ U-Th-Pb analysis of monazite by SHRIMP to constrain the emplacement age and hydrothermal history of the rare earth element-bearing Gifford Creek Carbonatite Complex in Western Australia, which has been linked to plume magmatism at ca. 1075 Ma. Monazite in carbonatites and related metasomatic rocks (fenites) from the carbonatite complex dates the initial emplacement of the carbonatite at 1361 ± 10 Ma (n = 22, MSWD = 0.91). The complex was subjected to multiple stages of magmatic/hydrothermal overprinting from ca. 1300 Ma to 900 Ma during later regional tectonothermal events. Carbonatite emplacement at ca. 1360 Ma appears to be an isolated igneous event in the region, and occurred about 300 million years before intrusion of the ca. 1075 Ma Warakurna large igneous province, thus precluding a genetic connection. The Gifford Creek Carbonatite Complex occurs within a major crustal suture, and probably formed in response to reactivation of this suture during plate reorganization. Our study demonstrates the veracity of monazite geochronology in determining the magmatic and hydrothermal histories of a carbonatite complex, critical for evaluating competing geodynamic models for carbonatites. The approach involving in situ SHRIMP U-Th-Pb dating of monazite from a wide spectrum of rocks in a carbonatite complex is best suited to establishing the intrusive age and hydrothermal history of carbonatites.
Abstract: Carbonatites are carbonate-dominated igneous rocks derived by low-degree partial melting of metasomatized mantle, although the geodynamic processes responsible for their emplacement into the crust are disputed. Current models favor either reactivation of lithospheric structures in response to plate movements, or the impingement of mantle plumes. Geochronology provides a means of testing these models, but constraining the age of carbonatites and related metasomatic events is rarely straightforward. We use in situ U-Th-Pb analysis of monazite by SHRIMP to constrain the emplacement age and hydrothermal history of the rare earth element-bearing Gifford Creek Carbonatite Complex in Western Australia, which has been linked to plume magmatism at ca. 1075 Ma. Monazite in carbonatites and related metasomatic rocks (fenites) from the carbonatite complex dates the initial emplacement of the carbonatite at 1361 ± 10 Ma (n = 22, MSWD = 0.91). The complex was subjected to multiple stages of magmatic/hydrothermal overprinting from ca. 1300 Ma to 900 Ma during later regional tectonothermal events. Carbonatite emplacement at ca. 1360 Ma appears to be an isolated igneous event in the region, and occurred about 300 million years before intrusion of the ca. 1075 Ma Warakurna large igneous province, thus precluding a genetic connection. The Gifford Creek Carbonatite Complex occurs within a major crustal suture, and probably formed in response to reactivation of this suture during plate reorganization. Our study demonstrates the veracity of monazite geochronology in determining the magmatic and hydrothermal histories of a carbonatite complex, critical for evaluating competing geodynamic models for carbonatites. The approach involving in situ SHRIMP U-Th-Pb dating of monazite from a wide spectrum of rocks in a carbonatite complex is best suited to establishing the intrusive age and hydrothermal history of carbonatites.
Geochimica et Cosmochimica Acta, Vol. 282, pp. 297-323.
Africa, East Africa
carbonatites
Abstract: Rare earth element (REE) enrichments in carbonatites are often described as resulting from late magmatic-hydrothermal or supergene processes. However, magmatic pre-enrichment linked to the igneous processes at the origin of carbonatites are likely to contribute to the REE fertilisation. Experimental constraints reveals that immiscibility processes between carbonate and silicate melts can lead to both REE enrichments and depletions in carbonatites making the magmatic processes controlling REE enrichments unclear.
We link REE contents of carbonatites to the magmatic stage at which carbonatites are separated from silicate magma in their course of differentiation. We present results of experiments made at pressure and temperature conditions of alkaline magmas and associated carbonatites differentiation (0.2-1.5 GPa; 725-975?°C; FMQ to FMQ?+?2.5), simultaneously addressing crystal fractionation of alkaline magmas and immiscibility between carbonate (calcio-carbonate type) and silicate melts (nephelinite to phonolite type). The experimental data shows that the degree of differentiation, controlling the chemical composition of alkaline melts, is a key factor ruling the REE concentration of the coexisting immiscible carbonate melts. In order to predict carbonate melt REE enrichments during alkaline magma differentiation, we performed a parameterisation of experimental data on immiscible silicate and carbonate melts, based exclusively on the silica content, the alumina saturation index and the alkali/alkaline-earth elements ratio of silicate melts. This parameterisation is applied to more than 1600 geochemical data of silicate magmas from various alkaline provinces (East African Rift, Canary and Cape Verde Islands) and show that REE concentrations of their potential coeval carbonatite melts can reach concentration ranges similar to those of highly REE enriched carbonatites (?REE?>?30 000?ppm) by immiscibility with phonolitic/phono-trachytic melt compositions, while more primitive alkaline magmas can only be immiscible with carbonatites that are not significantly enriched in REE.
India's changing place in global Proterozoic reconstructions: a review of geochronologic constraints and paleomagnetic poles from the Dharwar Bundelk hand and Marwar
Journal of Geodynamics, Vol. 50, 3-4, pp. 224-242.
Sanatmaria-Perez, D., Ruiz-Fuertes, J., Pena-Alvarez, M., Chulia-Jordan, R., Marquerno, T., Zimmer, D., Guterrez-Cano, V., Macleod, S., Gregoryanz, E., Popescue, C., Rodriguez-Herandez, P., Munoz, A.
Abstract: Calcium carbonate is a relevant constituent of the Earth’s crust that is transferred into the deep Earth through the subduction process. Its chemical interaction with calcium-rich silicates at high temperatures give rise to the formation of mixed silicate-carbonate minerals, but the structural behavior of these phases under compression is not known. Here we report the existence of a dense polymorph of Ca5(Si2O7)(CO3)2 tilleyite above 8 GPa. We have structurally characterized the two phases at high pressures and temperatures, determined their equations of state and analyzed the evolution of the polyhedral units under compression. This has been possible thanks to the agreement between our powder and single-crystal XRD experiments, Raman spectroscopy measurements and ab-initio simulations. The presence of multiple cation sites, with variable volume and coordination number (6-9) and different polyhedral compressibilities, together with the observation of significant amounts of alumina in compositions of some natural tilleyite assemblages, suggests that post-tilleyite structure has the potential to accommodate cations with different sizes and valencies.
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.
Abstract: The trace element composition of olivine is becoming increasingly important in petrological studies due to the ubiquity of olivine in the Earth's upper mantle and in primitive magmatic rocks. The LA-ICP-MS method allows for the routine analysis of trace elements in olivine to sub-ppm levels, but a major drawback of this method is the lack of knowledge about possible downhole fractionation effects when non matrix-matched calibration is used. In this contribution, we show that matrix-matched (i.e., olivine-based) calibration is preferable for small laser spot sizes (<100?µm) due to significant laser-induced inter-element fractionation between olivine and commonly used silicate glass calibration materials, e.g., NIST SRM 612, GSD-1G and BHVO-2G. As a result, we present two Mg-rich natural olivine standards (355OL and SC-GB) that have been characterized by independent methods (EPMA, solution ICP-MS), and by LA-ICP-MS in four different laboratories. These natural olivines have been used 1) as primary standards for the matrix-matched calibration of olivine samples for most elements of interest (e.g., Li, Na, Al, P, Ca, Sc, Ti, V, Cr, Mn, Co, Ni, Cu, Zn), and 2) as secondary standards to assess the accuracy of results. Comparison of olivine- and silicate glass-calibrated results for natural peridotitic olivine reveals that matrix-matched calibration is essential when using small laser spot sizes (<100?µm) in order to mitigate downhole fractionation effects for certain elements, especially Na, P, Mn, Co, Ni and Zn. If matrix-matched calibration is not feasible, we recommend that spot sizes of =100?µm, laser fluence of =4.0?J/cm2, and total laser shot counts of =250 (e.g., 5?Hz repetition rate for 50?s) are used in order to minimize fractionation effects between olivine and silicate glass calibration materials. We demonstrate the applicability of matrix-matched calibration on olivine from a suite of different mantle peridotite xenoliths sampled by kimberlites and alkali basalts from on-craton and off-craton localities.
Journal of African Earth Sciences, Vol. 146, pp. 28-47.
Africa, Cameroon
craton
Abstract: Field, microstructural, and anisotropy of magnetic susceptibility (AMS, magnetic fabrics) studies assessed the Pan-African deformational history and strain geometry at the southern margin of the Central African Fold Belt (CAFB) against the older, cratonic basement of the Congo Shield (CS). Reflected light microscopy and thermomagnetic studies supported the identification of magnetic minerals. Data cover a low angle thrust margin (Mbengis-Sangmelima area) in the east and high angle shear zones cutting the margin (Kribi area) in the west, at the Atlantic coast. In the CS basement units, magnetic anisotropy is generally higher than in the low grade Pan-African units. In the latter, early D1/D2 shortening produced a flat-lying magnetic foliation parallel with the regional trend of the belt, a shallow magnetic lineation, and mostly oblate fabrics. Subsequent D3 deformation is only of local importance in the Mbengis-Sangmelima area. The magnetic lineation shows distinct maxima in NNE-SSW direction, parallel with the low angle tectonic transport direction. In the Kribi area, the NNE-SSW trending Kribi-Campo shear zone (KCSZ) affected both older rocks and Pan-African high grade metapelites of the Yaoundé unit together with their basal thrust. The early planar fabric (S1) was overprinted during D2 folding under relatively high T conditions, and subsequent D3 wrenching. Magnetic fabrics document a progressive change from oblate towards prolate ellipsoids towards the KCSZ. Magnetic foliations with medium to steep dips curve into the N-S to NE-SW orientation of the KCSZ, lineations follow the same trend with shallow to medium plunges. This fabric implies that the KCSZ is a Pan-African strike-slip shear zone with a subordinate component of compression. Strike-slip tectonics in the west (KCSZ) and thrusting in the east imply N-S to NE-SW convergence during Pan-African terrane assembly against the present northern margin of the CS. In addition, the KCSZ may separate the CS from the São Francisco Craton in Brazil and thus be the northern part of a link connecting the CAFB to the West Congo Belt in the south. This putative Pan-African link separated the São Francisco Craton from the Congo Shield prior to Mesozoic Gondwana break-up.
Dyke Swarms of the World: a modern perspective, Srivastava et al. eds. Springer , pp. 263-314.
Africa, West Africa, South America
geochronology
Abstract: Eight different generations of dolerite dykes crosscutting the Paleoproterozoic basement in West Africa and one in South America were dated using the high precision U-Pb TIMS method on baddeleyite. Some of the individual dykes reach over 300 km in length and they are considered parts of much larger systems of mafic dyke swarms representing the plumbing systems for large igneous provinces (LIPs). The new U-Pb ages obtained for the investigated swarms in the southern West African Craton (WAC) are the following (oldest to youngest): 1791?±?3 Ma for the N010° Libiri swarm, 1764?±?4 Ma for the N035° Kédougou swarm, 1575?±?5 for the N100° Korsimoro swarm, ~1525-1529 Ma for the N130° Essakane swarm, 1521?±?3 Ma for the N90° Sambarabougou swarm, 915?±?7 Ma for the N070° Oda swarm, 867?±?16 Ma for the N355° Manso swarm, 202?±?5 Ma and 198?±?16 Ma for the N040° Hounde swarm, and 200?±?3 Ma for the sills in the Taoudeni basin. The last ones are related to the Central Atlantic Magmatic Province (CAMP) event. The Hounde swarm is oblique to the dominant radiating CAMP swarm and may be linked with the similar-trending elongate Kakoulima intrusion in Guinea. In addition, the N150° Käyser swarm (Amazonian craton, South America) is dated at 1528?±?2 Ma, providing a robust match with the Essakane swarm in a standard Amazonia-West African craton reconstruction, and resulting in a combined linear swarm >1500 km by >1500 km in extent. The Precambrian LIP barcode ages of c. 1790, 1765-1750, 1575, 1520, 915. 870 Ma for the WAC are compared with the global LIP record to identify possible matches on other crustal blocks, with reconstruction implications. These results contribute to the refinement of the magmatic ‘barcode’ for the West African and Amazonian cratons, representing the first steps towards plausible global paleogeographic reconstructions involving the West African and Amazonian cratons.
Abstract: A series of precise nondestructive analytical methods (Raman spectroscopy, cathodoluminescence, and EBSD—electron backscatter diffraction) has been employed to investigate the internal textures of kyanite porphyroblasts from diamondiferous and diamond-free ultrahigh-pressure metamorphic rocks (Kokchetav massif, Northern Kazakhstan). Such internal kyanite characteristics as twinning, radial fibrous pattern, and spotty zoning were identified by means of Raman and cathodoluminescence imaging, whereas an intergrowth of two kyanite crystals was distinguished only by Raman imaging. The EBSD analysis recorded an ~10-25° changing of orientations along the elongation in the investigated kyanite porphyroblasts. The absence of a radial fibrous pattern and a spotty zoning on the EBSD maps indicates that these textures are not related to variations in crystallographic orientation. The absence of clear zoning patterns (cores, mantles, and rims) on the Raman, cathodoluminescence, or EBSD maps of the kyanite porphyroblasts indicates the rapid single-stage formation of these porphyroblasts near the peak metamorphic conditions and the lack of recrystallization processes. The obtained results provide important implications for deciphering of mineral internal textures, showing that the data obtained by cathodoluminescence mapping can be clearly reproduced by Raman imaging, with the latter method occasionally being even more informative. This observation is of significant importance for the study of minerals that are unexposed on a thin section surface or Fe- and Ni-rich minerals that do not show luminescence emission. The combination of the Raman spectroscopic, cathodoluminescence, and EBSD techniques may provide better spatial resolution for distinguishing different domains and textural peculiarities of mineral than the selective application of individual approaches.
van den Heuvel, Q., Matveev, S., Drury, M., Gress, M., Chinn, I., Davies, G.
Genesis of diamond inclusions: an integrated cathodluminescence ( CL) and electron backscatter diffraction (EBSD) study on eclogitic and peridotitic inclusions and their diamond host.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 6564 Abstract
Abstract: The diamondiferous Letlhakane kimberlites are part of the Orapa kimberlite cluster (˜ 93.1 Ma) in north-eastern Botswana, located on the edge of the Zimbabwe Craton, close to the Proterozoic Magondi Mobile Belt. Here we report the first Re-Os ages of six individual eclogitic sulphide inclusions (3.0 to 35.7µg) from Letlhakane diamonds along with their rhenium, osmium, iridium and platinum concentrations, and carbon isotope, nitrogen content and N-aggregation data from the corresponding growth zones of the host diamonds. For the first time, Re-Os data will be compared to Sm-Nd ages of individual eclogitic silicate inclusions recovered from the same diamonds using a Triton Plus equipped with four 1013O amplifiers. The analysed inclusion set currently encompasses pairs of individual sulphides from two diamonds (LK040 sf4 & 5, LK113 sf1 & 2) and two sulphide inclusions from separate diamonds (LK048, LK362). Ongoing work will determine the Sm-Nd ages and element composition of multiple individual eclogitic garnets (LK113/LK362, n=4) and an eclogitic clinopyroxene (LK040) inclusion. TMA ages of the six sulphides range from 1.06 to 2.38 Ga (± 0.1 to 0.54 Ga) with Re and Os contents between 7 and 68 ppb and 0.03 and 0.3 ppb, respectively. The host diamond growth zones have low nitrogen abundances (21 to 43 ppm N) and high N-aggregation (53 to 90% IaB). Carbon isotope data suggests the involvement of crustal carbon (d13C between -19.3 to -22.7 ± 0.2 per mill) during diamond precipitation. Cathodoluminescence imaging of central plates from LK040 and LK113 displays homogenous internal structure with no distinct zonation. The two sulphide inclusions from LK040 define an 'isochron' of 0.92 ± 0.23 Ga (2SD) with initial 187Os/188Os = 1.31 ± 0.24. Sulphides from LK113 have clear imposed diamond morphology and indicate diamond formation at 0.93 ± 0.36 Ga (2SD) with initial 187Os/188Os = 0.69 ± 0.44. The variation in the initial 187Os/188Os does not justify including these inclusions (or any from other diamonds) on the same isochron and implies an extremely heterogeneous diamond crystallisation environment that incorporated recycled Os. C1-normalized osmium, iridium and platinum (PGE) compositions from the analysed sulphide inclusions display enrichment in Ir (3.4 to 33) and Pt (2.3 to 28.1) in comparison to eclogitic xenolith data from Orapa that are depleted relative to chondrite. The Re-Os isochrons determined in this study are within error of previously reported ages from the adjacent (˜40km) Orapa diamond mine (1.0 to 2.9 Ga) based on sulphide inclusions and a multi-point 990 ± 50 Ma (2SD) isochron for composite (n=730) silicate inclusions. Together with additional new Sm-Nd isochron age determinations from individual silicate inclusions from Letlhakane (2.3 ± 0.02 (n = 3); 1.0 ± 0.14 (n = 4) and 0.25 ± 0.04 Ga (n = 3), all 2SE) these data suggest a phase of Mesoproterozoic diamond formation as well as Neoarchean/Paleoproterozoic and Mesozoic diamond growth, in punctuated events spanning >2.0 Ga.
European Geosciences Union General Assembly 2017, Vienna April 23-28, 1p. 5540 Abstract
Africa, Botswana
Deposit - Letlhakane
Abstract: The diamondiferous Letlhakane kimberlites are part of the Orapa kimberlite cluster (˜ 93.1 Ma) in north-eastern Botswana, located on the edge of the Zimbabwe Craton, close to the Proterozoic Magondi Mobile Belt. Here we report the first Re-Os ages of six individual eclogitic sulphide inclusions (3.0 to 35.7µg) from Letlhakane diamonds along with their rhenium, osmium, iridium and platinum concentrations, and carbon isotope, nitrogen content and N-aggregation data from the corresponding growth zones of the host diamonds. For the first time, Re-Os data will be compared to Sm-Nd ages of individual eclogitic silicate inclusions recovered from the same diamonds using a Triton Plus equipped with four 1013O amplifiers. The analysed inclusion set currently encompasses pairs of individual sulphides from two diamonds (LK040 sf4 & 5, LK113 sf1 & 2) and two sulphide inclusions from separate diamonds (LK048, LK362). Ongoing work will determine the Sm-Nd ages and element composition of multiple individual eclogitic garnets (LK113/LK362, n=4) and an eclogitic clinopyroxene (LK040) inclusion. TMA ages of the six sulphides range from 1.06 to 2.38 Ga (± 0.1 to 0.54 Ga) with Re and Os contents between 7 and 68 ppb and 0.03 and 0.3 ppb, respectively. The host diamond growth zones have low nitrogen abundances (21 to 43 ppm N) and high N-aggregation (53 to 90% IaB). Carbon isotope data suggests the involvement of crustal carbon (d13C between -19.3 to -22.7 ± 0.2 per mill) during diamond precipitation. Cathodoluminescence imaging of central plates from LK040 and LK113 displays homogenous internal structure with no distinct zonation. The two sulphide inclusions from LK040 define an 'isochron' of 0.92 ± 0.23 Ga (2SD) with initial 187Os/188Os = 1.31 ± 0.24. Sulphides from LK113 have clear imposed diamond morphology and indicate diamond formation at 0.93 ± 0.36 Ga (2SD) with initial 187Os/188Os = 0.69 ± 0.44. The variation in the initial 187Os/188Os does not justify including these inclusions (or any from other diamonds) on the same isochron and implies an extremely heterogeneous diamond crystallisation environment that incorporated recycled Os. C1-normalized osmium, iridium and platinum (PGE) compositions from the analysed sulphide inclusions display enrichment in Ir (3.4 to 33) and Pt (2.3 to 28.1) in comparison to eclogitic xenolith data from Orapa that are depleted relative to chondrite. The Re-Os isochrons determined in this study are within error of previously reported ages from the adjacent (˜40km) Orapa diamond mine (1.0 to 2.9 Ga) based on sulphide inclusions and a multi-point 990 ± 50 Ma (2SD) isochron for composite (n=730) silicate inclusions. Together with additional new Sm-Nd isochron age determinations from individual silicate inclusions from Letlhakane (2.3 ± 0.02 (n = 3); 1.0 ± 0.14 (n = 4) and 0.25 ± 0.04 Ga (n = 3), all 2SE) these data suggest a phase of Mesoproterozoic diamond formation as well as Neoarchean/Paleoproterozoic and Mesozoic diamond growth, in punctuated events spanning >2.0 Ga.
Abstract: Precise dating of diamond growth is required to understand the interior workings of the early Earth and the deep carbon cycle. Here we report Sm-Nd isotope data from 26 individual garnet inclusions from 26 harzburgitic diamonds from Venetia, South Africa. Garnet inclusions and host diamonds comprise two compositional suites formed under markedly different conditions and define two isochrons, one Archaean (2.95?Ga) and one Proterozoic (1.15?Ga). The Archaean diamond suite formed from relatively cool fluid-dominated metasomatism during rifting of the southern shelf of the Zimbabwe Craton. The 1.8 billion years younger Proterozoic diamond suite formed by melt-dominated metasomatism related to the 1.1?Ga Umkondo Large Igneous Province. The results demonstrate that resolving the time of diamond growth events requires dating of individual inclusions, and that there was a major change in the magmatic processes responsible for harzburgitic diamond formation beneath Venetia from the Archaean to the Proterozoic.
Geophysical Research Abstracts www.researchgate.net, Vol. 20, EGU2018-128291p. Abstract
Africa, South Africa
diamond inclusions
Abstract: Changing recycling budgets of surface materials and volatiles by subduction of tectonic plates influence the compositions of Earth’s major reservoirs and affect climate throughout geological time. Fluids play a key role in processes governing subduction recycling, but quantifying the exact fate of volatiles introduced into the mantle at ancient and recent destructive plate boundaries remains difficult. Here, we report on the role of fluids and the fate of volatiles and other elements at two very different tectonic settings: 1) at subduction settings, and 2) within the subcontinental lithospheric mantle (SCLM). We will show how olivine-hosted melt inclusions from subduction zones and mineral inclusions in diamond from the SCLM are used to reveal how changing tectonic settings influence volatile cycles with time. Melt inclusions from the complex Italian post-collisional tectonic setting are used to identify changing subduction recycling through time. The use of CO2 in deeply trapped melt inclusions instead of in lavas or volcanic gases provides a direct estimate of deep recycling, minimizing possible effects of contamination during transfer through the crust. The aim is to distinguish if increased recycling of sediments from the down-going plate at continental subduction settings results in increased deep CO2 recycling or if the increased CO2 flux results from crustal degassing of the overriding plate. Both processes likely affected climate through Earth history but could thus far not be discriminated. The study of mineral inclusions and their host diamonds from the SCLM can link changes in the cycling of carbon-rich fluids and the time and process through which the carbon redistribution took place. We use Sm-Nd isotope techniques to date the mineral inclusions and use the carbon isotope data of the host diamonds to investigate the growth conditions. I will present case-studies of peridotitic and eclogitic diamonds from three mines in Southern Africa.
Abstract: The diamondiferous Jwaneng kimberlite cluster (~240 Ma) is located on the NW rim of the Archaean Kaapvaal Craton in central Botswana. Previous studies report eclogitic diamond formation in the late Archean (2.9 Ga) and in the Middle Proterozoic (1.5 Ga) involving different mantle and sedimentary components [1;2;3]. Here we report newly acquired Sm- Nd ages of individual eclogitic pyrope-almandine and omphacite inclusions along with their major element data and nitrogen data from the diamond hosts to re-examine Jwaneng’s diamond formation ages. The Sm-Nd isotope analyses were performed via TIMS using 1013O resistors [4]. An initial suite of three pyropealmandine and 14 omphacite inclusions yield 143Nd/144Nd from 0.51102±7 to 0.5155±5. 147Sm/144Nd vary from 0.024 to 0.469. Major element data defines two inclusion populations: (1) seven omphacites with high Mg#, high Cr# and one pyropealmandine with low-Ca define an isochron age of 1.93±0.16 Ga with ?Ndi= +3.5; (2) seven omphacites with low Mg#, low Cr# and two pyrope-almandines with low-Ca define an isochron age of 0.82±0.06 Ga with ?Ndi= +3.7. Nitrogen contents of corresponding diamond host growth zones in Group (1) are = 50 at.ppm whereas Group (2) range between 50 to 700 at.ppm with N-aggregation > 70 %B. Additional data used to define “co-genetic” inclusion suites include Sr-isotopes and trace elements of the inclusions and carbon isotopes of the diamond hosts. Re-Os data of coexisting sulphide inclusions from the same silicate-bearing diamonds further validates the ages and indicates more periods of diamond formation at Jwaneng than previously assumed. The integrated data indicate the possibility of an extensive Paleoproterozoic diamond-forming event in southern Africa.
Africa, Zimbabwe. Australia, Canada, Northwest Territories, South Africa, Botswana
deposit - Murowa, Argyle, Diavik, Venetia, Orapa
Abstract: FTIR maps of diamond plates, cut through the centre of growth, contain abundant information about changing defect concentrations from core to rim. These data can, in principle, be interpreted in terms of the variation in conditions of diamond growth and the temperatures experienced by the diamond during the period of mantle residence between growth and exhumation. Many diamonds show multiple growth zones that can be observed by cathodoluminescence. Importantly, the combination of nitrogen concentration and nitrogen aggregation measured by FTIR can be used to determine whether the growth zones are of similar or very different ages (Kohn et al., 2016). In this study, we use automated fitting of several thousand individual spectra within each FTIR map to define a model temperature for each pixel using the Python program, QUIDDIT. We then use a two-stage aggregation model to constrain potential temperature-time histories for each diamond. To take full advantage of the temperature history recorded by zoned diamonds, radiometric ages of inclusions are required. If the growth ages of each zone and the date of exhumation are well-known, then a model temperature can be calculated for each zone. The combination of zone-specific ages and improved quality and processing of FTIR spectra is able to provide unique new insights into the thermal history of diamondbearing lithospheric mantle. For the first time we will be able to use the N defects in diamonds to work out whether a particular location in the lithosphere has heated or cooled over long periods of geological time. The implications for the mechanism of formation of lithosphere will be discussed. We will illustrate the approach using examples of zoned diamonds from Murowa (Zimbabwe), Argyle (Australia), Diavik (Canada), Venetia (South Africa) and Orapa (Botswana).
Mineralogy and Petrology, doi.org/10.1007/s00710-018-0634-3 12p.
Africa, Botswana
deposit - Jwaneng
Abstract: To fully understand the implications of the compositional information recorded by inclusions in diamond it is vital to know if their growth was syn- or protogenetic and the extent to which they have equilibrated with diamond forming agents. The current paradigm is that the majority of inclusions in diamond are syngenetic but recently this assumption has been questioned. This study presents an integrated cathodoluminescence (CL) and electron backscatter diffraction (EBSD) study of 8 diamonds containing eclogitic inclusions: 19 pyrope-almandine garnets, 12 omphacitic clinopyroxenes, 4 sulphides, 1 coesite and 1 rutile from the Jwaneng diamond mine, Botswana. Diamond plates were sequentially polished to expose inclusions at different levels and CL imaging and EBSD were performed to constrain the relationship between diamond and inclusion growth. Despite complex growth and resorption, individual diamonds are single crystals with a homogeneous crystallographic orientation. All individual inclusions have homogeneous crystallographic orientation and no resolvable compositional zonation. The combined CL and EBSD data suggest that epitaxial inclusion-diamond growth is rare (none of 24 inclusions) and that the imposition of cubo-octahedral faces on inclusions does not necessarily result in epitaxy. Individual diamonds contain inclusions that record evidence of both syngentic and protogenetic relationships with the host diamond and in one case an inclusion appears syngenetic to the diamond core but protogenetic to the growth zone that surrounds 70% of the inclusion. These findings emphasise that inclusions in diamonds have multiple modes of origin and that in order to validate the significance of geochronological studies, further work is needed to establish that there is rapid chemical equilibration of protogenetic inclusions with diamond forming agents at mantle temperatures.
Geochimica et Cosmochimica Acta, 10.1016/j.gca.2020.10.010 35p. Pdf
Africa, Botswana
deposit - Jwaneng
Abstract: Constraining the formation age of individual diamonds from incorporated mineral inclusions and assessing the host diamonds’ geochemical characteristics allows determination of the complex history of diamond growth in the sub-continental lithospheric mantle (SCLM). It also provides the rare opportunity to study the evolution of the deep cycling of volatiles over time. To achieve these aims, Sm-Nd isotope systematics are presented for 36 eclogitic garnet and clinopyroxene inclusions from 16 diamonds from the Jwaneng mine, Botswana. The inclusions and host diamonds comprise at least two compositional suites that record different ‘mechanisms’ of diamond formation and define two isochrons, one Paleoproterozoic (1.8 Ga) and one Neoproterozoic (0.85 Ga). There are indications of at least three additional diamond-forming events whose ages currently cannot be well constrained. The Paleoproterozoic diamond suite formed by large-scale (> 100’s km), volatile-rich metasomatism related to formation and re-working of the Proto-Kalahari Craton. In contrast, the heterogeneous composition of the Neoproterozoic diamond suite indicates diamond formation on a small-scale, through local (< 10 km) equilibration of compositionally variable diamond-forming fluids in different eclogitic substrates during the progressive breakup of the Rodinia supercontinent. The results demonstrate that regional events appear to reflect the input of volatiles (i.e., carbon-bearing) derived from the asthenospheric mantle, whereas local diamond-forming events mainly promote the redistribution of volatiles within the SCLM. The occurrence of isotopically light carbon analysed in distinct growth zones from samples of this study (d13C < -21.1‰) provides further indication of a recycled origin for surface-derived carbon in some diamonds from Jwaneng. Determining Earth’s long-term deep carbon cycle using diamonds, however, requires an understanding of the nature and scale of specific diamond-forming events.
Abstract: Recent studies of mineral diversity and distribution lead to the prediction of >1563 mineral species on Earth today that have yet to be described-approximately one fourth of the 6394 estimated total mineralogical diversity. The distribution of these "missing" minerals is not uniform with respect to their essential chemical elements. Of 15 geochemically diverse elements (Al, B, C, Cr, Cu, Mg, Na, Ni, P, S, Si, Ta, Te, U, and V), we predict that approximately 25% of the minerals of Al, B, C, Cr, P, Si, and Ta remain to be described - a percentage similar to that predicted for all minerals. Almost 35% of the minerals of Na are predicted to be undiscovered, a situation resulting from more than 50% of Na minerals being white, poorly crystallized, and/or water soluble, and thus easily overlooked. In contrast, we predict that fewer than 20% of the minerals of Cu, Mg, Ni, S, Te, U, and V remain to be discovered. In addition to the economic value of most of these elements, their minerals tend to be brightly colored and/or well crystallized, and thus likely to draw attention and interest. These disparities in percentages of undiscovered minerals reflect not only natural processes, but also sociological factors in the search, discovery, and description of mineral species.
Geochemical Perspective Letters, Vol. 10, pp. 43-48. doi:10.7185/ geochemlet.1904
Mantle
xenoliths
Abstract: Heat flow studies suggest that the lower crust has low concentrations of heat-producing elements. This could be due to either (i) greater fractions of basaltic rock at depth or (ii) metamorphic depletion of radioactive elements from rocks with more evolved (andesitic to granodioritic) compositions. However, seismic data suggest that lower crust is not predominantly basaltic, and previous studies (using Pb and Sr isotopes) have shown that lower crustal rocks have experienced significant losses of U and Rb. This loss, however, is poorly constrained for K, which is inferred to be the most important source of radioactive heat in the earliest crust. Our high precision Ca isotope measurements on a suite of granulite facies rocks and minerals from several localities show that significant losses of K (~60 % to >95 %) are associated with high temperature metamorphism. These results support models whereby reduction of heat production from the lower crust, and consequent stabilisation of continental cratons in the Precambrian, are largely due to high temperature metamorphic processes. Relative changes in whole rock K/Ca suggest that 20-30 % minimum (granitic) melt removal can explain the K depletions.
Geochimica et Cosmochimica Acta, Vol. 238, pp. 477-495.
Mantle
carbon
Abstract: Constraining carbon (C) fractionation between silicate magma ocean (MO) and core-forming alloy liquid during early differentiation is essential to understand the origin and early distribution of C between reservoirs such as the crust-atmosphere, mantle, and core of Earth and other terrestrial planets. Yet experimental data at high pressure (P)-temperature (T) on the effect of other light elements such as sulfur (S) in alloy liquid on alloy-silicate partitioning of C and C solubility in Fe-alloy compositions relevant for core formation is lacking. Here we have performed multi-anvil experiments at 6-13?GPa and 1800-2000?°C to examine the effects of S and Ni on the solubility limit of C in Fe-rich alloy liquid as well as partitioning behavior of C between alloy liquid and silicate melt (). The results show that C solubility in the alloy liquid as well as decreases with increasing in S content in the alloy liquid. Empirical regression on C solubility in alloy liquid using our new experimental data and previous experiments demonstrates that C solubility significantly increases with increasing temperature, whereas unlike in S-poor or S-free alloy compositions, there is no discernible effect of Ni on C solubility in S-rich alloy liquid. Our modelling results confirm previous findings that in order to satisfy the C budget of BSE, the bulk Earth C undergoing alloy-silicate fractionation needs to be as high as those of CI-type carbonaceous chondrite, i.e., not leaving any room for volatility-induced loss of carbon during accretion. For Mars, on the other hand, an average single-stage core formation at relatively oxidized conditions (1.0 log unit below IW buffer) with 10-16?wt% S in the core could yield a Martian mantle with a C budget similar to that of Earth’s BSE for a bulk C content of ~0.25-0.9?wt%. For the scenario where C was delivered to the proto-Earth by a S-rich differentiated impactor at a later stage, our model calculations predict that bulk C content in the impactor can be as low as ~0.5?wt% for an impactor mass that lies between 9 and 20% of present day Earth’s mass. This value is much higher than 0.05-0.1?wt% bulk C in the impactor predicted by Li et al. (Li Y., Dasgupta R., Tsuno K., Monteleone B., and Shimizu N. (2016) Carbon and sulfur budget of the silicate Earth explained by accretion of differentiated planetary embryos. Nat. Geosci.9, 781-785) because C-solubility limit of 0.3?wt% in a S-rich alloy predicted by their models is significantly lower than the experimentally derived C-solubility of ~1.6?wt% for the relevant S-content in the core of the impactor.
Abstract: Earth’s status as the only life-sustaining planet is a result of the timing and delivery mechanism of carbon (C), nitrogen (N), sulfur (S), and hydrogen (H). On the basis of their isotopic signatures, terrestrial volatiles are thought to have derived from carbonaceous chondrites, while the isotopic compositions of nonvolatile major and trace elements suggest that enstatite chondrite-like materials are the primary building blocks of Earth. However, the C/N ratio of the bulk silicate Earth (BSE) is superchondritic, which rules out volatile delivery by a chondritic late veneer. In addition, if delivered during the main phase of Earth’s accretion, then, owing to the greater siderophile (metal loving) nature of C relative to N, core formation should have left behind a subchondritic C/N ratio in the BSE. Here, we present high pressure-temperature experiments to constrain the fate of mixed C-N-S volatiles during core-mantle segregation in the planetary embryo magma oceans and show that C becomes much less siderophile in N-bearing and S-rich alloys, while the siderophile character of N remains largely unaffected in the presence of S. Using the new data and inverse Monte Carlo simulations, we show that the impact of a Mars-sized planet, having minimal contributions from carbonaceous chondrite-like material and coinciding with the Moon-forming event, can be the source of major volatiles in the BSE.
Geochimica et Cosmochimica Acta, Vol. 251. pp. 87-115.
Mantle
nitrogen
Abstract: Nitrogen, the most dominant constituent of Earth’s atmosphere, is critical for the habitability and existence of life on our planet. However, its distribution between Earth’s major reservoirs, which must be largely influenced by the accretion and differentiation processes during its formative years, is poorly known. Sequestration into the metallic core, along with volatility related loss pre- and post-accretion, could be a critical process that can explain the depletion of nitrogen in the Bulk Silicate Earth (BSE) relative to the primitive chondrites. However, the relative effect of different thermodynamic parameters on the alloy-silicate partitioning behavior of nitrogen is not well understood. Here we present equilibrium partitioning data of N between alloy and silicate melt () from 67 new high pressure (P?=?1-6?GPa)-temperature (T?=?1500-2200?°C) experiments under graphite saturated conditions at a wide range of oxygen fugacity (logfO2?~??IW -4.2 to -0.8), mafic to ultramafic silicate melt compositions (NBO/T?=?0.4 to 2.2), and varying chemical composition of the alloy melts (S and Si contents of 0-32.1?wt.% and 0-3.1?wt.%, respectively). Under relatively oxidizing conditions (~?IW -2.2 to -0.8) nitrogen acts as a siderophile element ( between 1.1 and 52), where decreases with decrease in fO2 and increase in T, and increases with increase in P and NBO/T. Under these conditions remains largely unaffected between S-free conditions and up to ~17?wt.% S content in the alloy melt, and then drops off at >~20?wt.% S content in the alloy melt. Under increasingly reduced conditions (<~?IW -2.2), N becomes increasingly lithophile ( between 0.003 and 0.5) with decreasing with decrease in fO2 and increase in T. At these conditions, fO2 along with Si content of the alloy under the most reduced conditions (<~?IW -3.0), is the controlling parameter with T playing a secondary role, while, P, NBO/T, and S content of the alloy have minimal effects. A multiple linear least-squares regression parametrization for based on the results of this study and previous studies suggests, in agreement with the experimental data, that fO2 (represented by Si content of the alloy melt and FeO content of the silicate melt), followed by T, has the strongest control on . Based on our modeling, to match the present-day BSE N content, impactors that brought N must have been moderately to highly oxidized. If N bearing impactors were reduced, and/or there was significant disequilibrium core formation, then the BSE would be too N-rich and another mechanism for N loss, such as atmospheric loss, would be required.
Geochimica et Cosmochimica Acta, Vol. 251, pp. 87-115.
Mantle
nitrogen
Abstract: Nitrogen, the most dominant constituent of Earth’s atmosphere, is critical for the habitability and existence of life on our planet. However, its distribution between Earth’s major reservoirs, which must be largely influenced by the accretion and differentiation processes during its formative years, is poorly known. Sequestration into the metallic core, along with volatility related loss pre- and post-accretion, could be a critical process that can explain the depletion of nitrogen in the Bulk Silicate Earth (BSE) relative to the primitive chondrites. However, the relative effect of different thermodynamic parameters on the alloy-silicate partitioning behavior of nitrogen is not well understood. Here we present equilibrium partitioning data of N between alloy and silicate melt () from 67 new high pressure (P?=?1-6?GPa)-temperature (T?=?1500-2200?°C) experiments under graphite saturated conditions at a wide range of oxygen fugacity (logfO2?~??IW -4.2 to -0.8), mafic to ultramafic silicate melt compositions (NBO/T?=?0.4 to 2.2), and varying chemical composition of the alloy melts (S and Si contents of 0-32.1?wt.% and 0-3.1?wt.%, respectively). Under relatively oxidizing conditions (~?IW -2.2 to -0.8) nitrogen acts as a siderophile element ( between 1.1 and 52), where decreases with decrease in fO2 and increase in T, and increases with increase in P and NBO/T. Under these conditions remains largely unaffected between S-free conditions and up to ~17?wt.% S content in the alloy melt, and then drops off at >~20?wt.% S content in the alloy melt. Under increasingly reduced conditions (<~?IW -2.2), N becomes increasingly lithophile ( between 0.003 and 0.5) with decreasing with decrease in fO2 and increase in T. At these conditions, fO2 along with Si content of the alloy under the most reduced conditions (<~?IW -3.0), is the controlling parameter with T playing a secondary role, while, P, NBO/T, and S content of the alloy have minimal effects. A multiple linear least-squares regression parametrization for based on the results of this study and previous studies suggests, in agreement with the experimental data, that fO2 (represented by Si content of the alloy melt and FeO content of the silicate melt), followed by T, has the strongest control on . Based on our modeling, to match the present-day BSE N content, impactors that brought N must have been moderately to highly oxidized. If N bearing impactors were reduced, and/or there was significant disequilibrium core formation, then the BSE would be too N-rich and another mechanism for N loss, such as atmospheric loss, would be required.
Chemical composition, volatile components, and trace elements in melts of the Karymskii volcanic centre, Kamchatka and Golovnin a volcano, Kunashir Island....
Vladykin, N.V., Deep Seated Magmatism: its sources and plumes, pp. 104-127.
Evolution of deep crustal roots of the Arhangelsk Diamondiferous province: evidences from crustal xenoliths and xenocrysts from Devonian kimberlite pipes.
Abstract: The model, which will incorporate 227 million surface wave measurements, could help with everything from earthquake characterization to neutrino geosciences.
Abstract: Bolide impact is a ubiquitous geological process in the Solar System, which produced craters and basins filled with impact melt sheets on the terrestrial planets. However, it remains controversial whether these sheets were able to undergo large-scale igneous differentiation, or not. Here, we report on the discovery of large discrete bodies of melanorites that occur throughout almost the entire stratigraphy of the 1.85-billion-year-old Sudbury Igneous Complex (SIC) - the best exposed impact melt sheet on Earth - and use them to reaffirm that conspicuous norite-gabbro-granophyre stratigraphy of the SIC is produced by fractional crystallization of an originally homogeneous impact melt of granodioritic composition. This implies that more ancient and compositionally primitive Hadean impact melt sheets on the Earth and other terrestrial planets also underwent large-volume igneous differentiation. The near-surface differentiation of these giant impact melt sheets may therefore have contributed to the evolution and lithological diversity of the proto-crust on terrestrial planets.
Edwards, D., Rock, N.M.S., Taylor, W.R., Griffin, B.J., Sun, S-S.
The Aries Diamondiferous kimberlite pipe, central Kimberley block, westernAustralia: mineralogy, petrology and geochem. of the pipe rock and indicators
Proceedings of Fifth International Kimberlite Conference held Araxa June 1991, Servico Geologico do Brasil (CPRM) Special, pp. 82-84
Mineral chemistry and zircon geochronology of xenocrysts and altered mantle and crustal xenoliths from the Aries micaceous kimberlite: constraints age..
Downes, P.J., Demeny, A., Czuppon, G., Jacques, A.L., Verrall, M., Sweetapple, M., Adams, D., McNaughton, N.J., Gwalani, L.G., Griffin, B.J.
Stable H-C-O isotope and trace element geochemistry of the Cummins Range carbonatite complex, Kimberley region Western Australia: implications for hydrothermal REE mineralization, carbonatite evolution and mantle source regions.
Downes, P.J., Demeny, A., Czuppon, G., Jaques, A.L., Verrall, M., Sweetapple, M., Adams, D., McNaughton, N.J., Gwalani, L.G., Griffin, B.J.
Stable H-C-O isotope and trace element geochemistry of the Cummins Range carbonatite complex, Kimberley region western Australia: implications for hydrothermal REE mineralization, carbonatite evolution and mantle source regions.
