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The Sheahan Diamond Literature Reference Compilation - Technical, Media and Corporate Articles based on Major Region - Island
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 announcements called 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 Region Index
Sheahan Diamond Literature Reference Compilation - Scientific Articles by Author for all years
Each article reference in the SDLRC is tagged with one or more key words assigned by Pat Sheahan to highlight the main topics of the article. In addition most references have been tagged with one or more region words. In an effort to make it easier for users to track down articles related to a specific region, KRO has extracted these region words and developed a list of major region words presented in the Major Region Index to which individual region words used in the article reference have been assigned. Each individual Region Report contains in chronological order all the references with a region word associated with the Major Region word. Depending on the total for each reference type - technical, media and corporate - the references will be either in their own technical, media or corporate Region Report, or combined in a single report. Where there is a significant number of technical references there will be a technical report dedicated to the technical articles while the media and corporate references are combined in a separate region report. References that were added in the most recent monthly update are highlighted in yellow within the Region Report. The Major Region words have been defined by a scale system of "general", "continent", "country", "state or province" and "regional". Major Region words at the smaller scales have been created only when there are enough references to make isolating them worthwhile. References not tagged with a Region are excluded, and articles with a region word not matched with a Major Region show up in the "Unknown" report.
Kimberlite - diamondiferous
Lamproite - diamondiferous
Lamprophyre - diamondiferous
Other - diamondiferous
Kimberlite - non diamondiferous
Lamproite - non diamondiferous
Lamprophyre - non diamondiferous
Other - non diamondiferous
Kimberlite - unknown
Lamproite - unknown
Lamprophyre - unknown
Other - unknown
Future Mine
Current Mine
Former Mine
Click on icon for details about each occurrence. Works best with Google Chrome.
CITATION: Faure, S, 2010, World Kimberlites CONSOREM Database (Version 3), Consortium de Recherche en Exploration Minérale CONSOREM, Université du Québec à Montréal, Numerical Database on consorem.ca. NOTE: This publicly available database results of a compilation of other public databases, scientific and governmental publications and maps, and various data from exploration companies reports or Web sites, If you notice errors, have additional kimberlite localizations that should be included in this database, or have any comments and suggestions, please contact the author specifying the ID of the kimberlite: [email protected]
Dunitification of mantle lithosphere below the Society Archipelago:evidence for magma -mantle thermal and chemical transfers through xenoliths From the Papenoo Vall
Journal of Geodynamics, Vol. 13, No. 2-4, pp. 221-252
On the scale of heterogeneities in clinopyroxenes of spinel lherzolite xenoliths from Oahu, Hawaii: implications for non-modal advection-diffusion controlled trace e
Proceedings of Fifth International Kimberlite Conference held Araxa June 1991, Servico Geologico do Brasil (CPRM) Special, pp. 356-358
Ephemeral carbonate melts in the upper mantle; carbonate silicate immiscibility in microveins and inclusions within spinel peridotite xenoliths, la Gomera
European Journal of Mineralogy, Vol. 14, 5, pp. 891-904.
Compositional variations (major and trace elements) of clinopyroxene and Ti and radite from pyroxenite, ijolite and nepheline syenite, Alno Island, Sweden.
Bonadiman, C., Beccaluva, L., Coltort, M., Siena, F.
Kimberlite like metasomatism and garnet signature in spinel peridotite xenoliths from Sal, Cape Verde Archipelago: relics of subcontinental mantle domain.
Constraints on the coupled thermal evolution of the Earth's core and mantle, the age of the inner core and the origin of the 186 Os 188 Os core signal in plume..
Earth and Planetary Science Letters, In press - available
United States, Hawaii
Geothermometry - potassium, not specific to diamonds
Casillas, R., Demeny, A., Nagy, G., Ahijado, A., Fernandez, C.
Metacarbonatites in the Basal Complex of Fuerteventura ( Canary Islands). The role of fluid/rock interactions during contact metamorphism and anatexis.
Mourao, C., Mata, J., Doucekance, R., Madeira, J., Millet, M-A., Moreira, M.
Geochemical temporal evolution of Brava Island magmatism: constraints on the variability of Cape Verde mantle sources and on carbonatite-silicate magma link.
Mourao, C., Moreira, M., Mata, J., Raquin, A., Madeira, J.
Primary and secondary processes constraining the noble gas isotopic signatures of carbonatites and silicate rocks from Brava Island: evidence for a lower mantle origin of the Cape Verde Plume.
Contributions to Mineralogy and Petrology, Vol. 163, 6, pp. 995-1009.
Contributions to Mineralogy and Petrology, Vol. 171, pp. 43-50.
Europe, Cape Verde Islands
Carbonatite
Abstract: The carbonatites of Brava Island, Cape Verde hot spot, allow to investigate whether they represent small mantle melt fractions or form through extreme fractionation and/or liquid immiscibility from CO2-bearing silicate magmas. The intrusive carbonatites on Brava Island are part of a strongly silica-undersaturated pyroxenite, ijolite, nephelinite, nepheline syenite, combeite-foiditite, carbonatite series. The major and trace element composition of this suite is reproduced by a model fractionating olivine, clinopyroxene, perovskite, biotite, apatite, titanite, sodalite and FeTi oxides, all present as phenocrysts in the rocks corresponding to their fractionation interval. Fractionation of ~90 wt% crystals reproduces the observed geochemical trend from the least evolved ultramafic dikes (bulk X Mg = 0.64) to syenitic compositions. The modelled fractional crystallization leads to alkali enrichment, driving the melt into the carbonatite-silicate miscibility gap. An initial CO2 content of 4000 ppm is sufficient to saturate in CO2 at the point where the rock record suggests continuing unmixing carbonatites from nephelinites to nepheline syenites after 61 wt% fractionation. Such immiscibility is also manifested in carbonatite and silicate domains on a hand-specimen scale. Furthermore, almost identical primary clinopyroxene, biotite and carbonate compositions from carbonatites and nephelinites to nepheline syenites substantiate their conjugate character and our unmixing model. The modelled carbonatite compositions correspond to the natural ones except for their much higher alkali contents. The alkali-poor character of the carbonatites on Brava and elsewhere is likely a consequence of the release of alkali-rich CO2 + H2O fluids during final crystallization, which cause fenitization in adjacent rocks. We propose a general model for carbonatite generation during alkaline magmatism, where the fractionation of heavily Si-undersaturated, alkaline parent melts results in alkali and CO2 enrichment in the evolving melt, ultimately leading to immiscibility between carbonatites and evolved Si-undersaturated alkaline melts. Early saturation in feldspathoids or feldspars would limit alkali enrichment preventing the formation of carbonatites. The complete and continuous fractionation line from almost primitive melts to syenitic compositions on Brava underlines the possibly important role of intrusives for hot spot volcanism.
Nature Communications, Jan. 31, doi 10:1038/ncomms1048
Africa, Mauritius
Hot spots
Abstract: A fragment of continental crust has been postulated to underlie the young plume-related lavas of the Indian Ocean island of Mauritius based on the recovery of Proterozoic zircons from basaltic beach sands. Here we document the first U-Pb zircon ages recovered directly from 5.7?Ma Mauritian trachytic rocks. We identified concordant Archaean xenocrystic zircons ranging in age between 2.5 and 3.0?Ga within a trachyte plug that crosscuts Older Series plume-related basalts of Mauritius. Our results demonstrate the existence of ancient continental crust beneath Mauritius; based on the entire spectrum of U-Pb ages for old Mauritian zircons, we demonstrate that this ancient crust is of central-east Madagascar affinity, which is presently located ?700?km west of Mauritius. This makes possible a detailed reconstruction of Mauritius and other Mauritian continental fragments, which once formed part of the ancient nucleus of Madagascar and southern India.
Abstract: Estimates of carbon concentrations in Earth’s mantle vary over more than an order of magnitude, hindering our ability to understand mantle structure and mineralogy, partial melting, and the carbon cycle. CO2 concentrations in mantle-derived magmas supplying hotspot ocean island volcanoes yield our most direct constraints on mantle carbon, but are extensively modified by degassing during ascent. Here we show that undegassed magmatic and mantle carbon concentrations may be estimated in a Bayesian framework using diverse geologic information at an ocean island volcano. Our CO2 concentration estimates do not rely upon complex degassing models, geochemical tracer elements, assumed magma supply rates, or rare undegassed rock samples. Rather, we couple volcanic CO2 emission rates with probabilistic magma supply rates, which are obtained indirectly from magma storage and eruption rates. We estimate that the CO2 content of mantle-derived magma supplying Hawai‘i’s active volcanoes is 0.97?0.19+0.25 wt% -roughly 40% higher than previously believed-and is supplied from a mantle source region with a carbon concentration of 263?62+81?ppm. Our results suggest that mantle plumes and ocean island basalts are carbon-rich. Our data also shed light on helium isotope abundances, CO2/Nb ratios, and may imply higher CO2 emission rates from ocean island volcanoes.
Abstract: Estimates of carbon in the deep mantle vary by more than an order of magnitude. Coupled volcanic CO2 emission data and magma supply rates reveal a carbon-rich mantle plume source region beneath Hawai'i with 40% more carbon than previous estimates.
Geochemical Perspectives Letters, Vol. 3, pp. 230-237.
Canada, Quebec, Anticosti Island
carbon cycle
Abstract: Chemical weathering of silicate rocks is a primary drawdown mechanism of atmospheric carbon dioxide. The processes that affect weathering are therefore central in controlling global climate. A temperature-controlled “weathering thermostat” has long been proposed in stabilising long-term climate, but without definitive evidence from the geologic record. Here we use lithium isotopes (?7Li) to assess the impact of silicate weathering across a significant climate-cooling period, the end-Ordovician Hirnantian glaciation (~445 Ma). We find a positive ?7Li excursion, suggestive of a silicate weathering decline. Using a coupled lithium-carbon model, we show that initiation of the glaciation was likely caused by declining CO2 degassing, which triggered abrupt global cooling, and much lower weathering rates. This lower CO2 drawdown during the glaciation allowed climatic recovery and deglaciation. Combined, the data and model provide support from the geological record for the operation of the weathering thermostat.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (São Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the São Miguel Island.
Abstract: A detailed electron microprobe study has been carried out on the compositional variations of mica and apatite from carbonatites, phoscorites and associated pyroxenites (and fenites) of the Loolekop deposit, Palabora Carbonatite Complex (South Africa). Mica in pyroxenites and fenites is Mg-rich biotite, whilst micas in carbonatites and phoscorites are compositionally diverse including phlogopite, Ba-rich phlogopite (up to 30% kinoshitalite component), IVAl-rich phlogopite (up to 30% eastonite component) and tetraferriphlogopite. The various types of phlogopites are interpreted as orthomagmatic phases, whereas tetraferriphlogopite precipitation was a late-magmatic to hydrothermal process that additionally introduced REE into the system. Orthomagmatic apatite is generally REE- and Sr-poor fluorapatite and does not show large compositional differences between rock types. Apatite associated with the late-stage tetraferriphlogopite mineralization reaches higher levels of REE (up to 4.9?wt%), Si (up to 1.5?wt% SiO2), Sr (up to 2.6?wt% SrO) and Na (up to 1.0?wt% Na2O). The compositional variation of micas and apatites, which is affiliated with distinct rock types, reflects the multi-stage evolution of the Loolekop deposit and provides detailed insight into the relationships of the carbonatite-phoscorite assemblage. The obtained data support the separation of phoscorite and carbonatite by immiscibility from a common parental magma, which may happen due to a decrease of temperature and/or pressure during the ascent of the magma. This results in a density contrast between the carbonatitic and phoscoritic components that will lead to descending phoscorite accumulations at the outer zones of the magma channel and a jet-like ascent (further promoted by its extremely low viscosity) of the carbonatite magma. The genetic model deduced here explains the peculiar association of carbonatites, phoscorites and silicate rocks in many alkaline complexes worldwide.
Abstract: Our discovery of moissanite grains in a peralkaline syenite from the Água de Pau Volcano (São Miguel, Azores Islands, Portugal) represents the first report of this mineral in present day oceanic geodynamic settings. Raman spectroscopy and single-crystal X-ray diffraction show the presence of both the 6H and 4H polytypes with the predominance of the first one. The distribution of trace elements is homogeneous, except for Al and V. Azorean moissanite often hosts rounded inclusions of metallic Si and other not yet identified metallic alloys. A process involving a flushing of CH4-H2 ultra-reducing fluids in the alkaline melts might be considered as a possible mechanism leading to the formation of natural SiC, thus calling for strongly reducing conditions that were locally met in the crust-mantle beneath the São Miguel Island.
Abstract: The interaction of hydrous fluids and melts with dry rocks of the lithospheric mantle inevitably modifies their viscoelastic and chemical properties due to the formation of compositionally distinct secondary phases. In addition, melt percolation and the associated metasomatic alteration of mantle rocks may also facilitate modification of the pre-existing rock texture and olivine crystallographic preferred orientation (CPO) and thus seismic properties. Here we explore the relationship between mantle metasomatism, deformation and seismic anisotropy using subduction-related mantle xenoliths from the Penghu Islands, western Taiwan. The investigated xenoliths have equilibrated at upper lithospheric mantle conditions (879?°C to 1127?°C) based on pyroxene geothermometry and show distinct variations in clinopyroxene chemical composition, texture and olivine CPO allowing for the classification of two distinct groups. Group 1 xenoliths contain rare earth element (REE) depleted clinopyroxene, show a porphyroclastic texture and olivine grains are mostly characterized by [100]-axial pattern symmetries. In contrast, REE-enriched clinopyroxene from Group 2 xenoliths occur in a fine-grained equigranular texture and coexisting olivine frequently displays [010]-axial pattern symmetries. The clinopyroxene compositions are indicative of cryptic and modal to stealth metasomatic alteration of Group 1 and Group 2 xenoliths, respectively. Furthermore, the observed olivine [100]-axial pattern of Group 1 xenoliths reflects deformation by dislocation creep at high temperature, low pressure and dry conditions, whereas olivine [010]-axial patterns of Group 2 xenoliths imply activation of olivine [001] glide planes along preferentially wet (010) grain boundaries. This correlation indicates that the variation in olivine CPO symmetry from [100]- to [010]-axial pattern in Penghu xenoliths results from deformation and intra-crystalline recovery by subgrain rotation during metasomatic alteration induced by melt percolation. The microstructural observations and olivine CPO combined with petrological and geochemical data suggest that Group 1 xenoliths preserve microstructural and chemical characteristics of an old, probably Proterozoic lithosphere, while Group 2 xenoliths record localized Miocene deformation associated with wall-rock heating and metasomatism related to melt circulation. Furthermore, the observed transition of olivine CPO from [100]-axial pattern to [010]-axial pattern by deformation in the presence of variable melt fractions and associated metasomatic alteration can be inferred to modify the physical properties of mantle rocks.
Geochimica et Cosmochimica Acta, Vol. 254, pp. 21-39.
New Zealand
metasomatism
Abstract: Megacrystic zircon grains from alkaline basaltic fields are rare but can provide fundamental insights into mantle metasomatic processes. Here, we report in-situ U-Pb ages, trace element concentrations and hafnium and oxygen isotopes for fourteen zircon megacrysts from two intraplate alkaline basalt locations in New Zealand. U-Pb ages indicate the zircons crystallised between 12.1 and 19.8 Ma. Zircon oxygen isotopic compositions range from low to mantle-like compositions (grain average ? ¹? O = 3.8-5.1‰). Hafnium isotopes (?Hf (t) = +3.3 to +10.4) mostly overlap with intraplate mafic rocks and clinopyroxene in metasomatized peridotitic mantle xenoliths but show no correlation with most trace element parameters or oxygen isotopes. The zircons are interpreted to have formed by the reaction between low-degree melts derived from pre-existing mantle metasomes and the depleted mantle lithosphere prior to eruption and transport to the surface. The low Hf concentration, an absence of Eu anomalies, and elevated U/Yb compared to Nb/Yb in the megacrystic zircons are interpreted to show that the source metasomes comprised subduction- and carbonatite-metasomatised lithospheric mantle. As these trace element characteristics are common for megacrystic zircon in intra-plate basaltic fields globally, they suggest the prevalence of subduction- and carbonatite-metsasomatised mantle under these intraplate volcanic regions. The unusually low ? ¹? O was likely present prior to metasomatic enrichment and may have resulted from high-temperature hydrothermal alteration during initial mantle lithosphere formation at a mid ocean ridge or, possibly, during subduction-related processes associated with continent formation. The combination of proportionally varied contributions from carbonatite- and subduction-metasomatised lithospheric melts with asthenospheric melts may explain the variety of primitive intraplate basalt compositions, including low ? ¹? O reported for some local intraplate lavas.
Abstract: In 1992 Rampino noticed a large, almost circular negative gravity anomaly (~30 mGal) on the Falkland Plateau to the WNW of Malvinas Islands/Falklnad Islands using satellite data then available, and speculated that it might be associated with a large (~250 km wide?) buried impact structure. In some more recent compilations Rocca & Presser (2015) and Rocca et al. (2017) was attended the Malvinas Islands/Falklnad Islands “buried impact structure” with particular care; but also these works was harshly criticized. The present text, which is an advance to demonstrate the certain possibilities that this Malvinas Islands/Falklnad Islands It could really be a very probable mega impact structure, gathers shows and evaluates the existing and available indirect information; like gravimetry (Isostasy, Free-air and Bouguer); seismic reflection (Geco Prakla); and, even commenting aspects of its magnetic behavior and its local geology. In all gravimetric analyses from the Malvinas Islands/Falklnad Islands “buried impact structure” it can be shown that an annulus of positive gravity anomaly surrounding a circular oval depression of negative (isostasy and Free-air)/much lower (Bouguer) values gravity anomaly. The most relevant gravimetric information would be the near circular to oval Bouguer gravity low anomaly (with a minimum value of ~150 mGal) surrounded by at least circular ~255 kilometers wide circular ring of positive gravity anomaly (maximum ~225 mGal); a very high values of Bouguer anomaly that are highly compatible with what is expected to be found in mega impact structures. The Malvinas probable impact structure shows almost 100 mGal superior to the volcanic complex of Iceland; so it seems obvious that Malvinas probable impact structure moves away from a speculation by mega-paleo-volcano origin. When gravimetrically modeled, a probable peak ring of ~255 km is evidenced; as well as, the inferred the ~550 km probable rim-crest; configuration that reproduces an almost perfect and symmetrical modeling of a very probable giant impact structure with its clear visible the very probable elements: rim crest-annulus basin-peak ring-central basin-peak ring-annulus basin-rim crest. Four Geco Prakla seismic reflection lines on the area located to the SW of the potential peak ring show a vertical and disturbed crystalline basement (the “peak ring”); in three of them, the “central basin” what would it be filled with sediments after impact (probable ejecta). Using the empirical formula of Assumpção et al. (2013) calculation for crustal thickness could be found very clearly strong CT distortion along Malvinas very probable giant impact structure: around 3400-4000 meters; as is to be expected in terrestrial mega impact structure. Harness the EMAG2v3 a global Earth Magnetic Anomaly Grid compiled from satellite (Meyer et al., 2017) for the Malvinas very probable giant impact structure a well superior anomaly was found and better definition than observed, using the same information, to the one characterized by the impact crater Chicxulub. The geological map of the Falkland Islands Government that was placed on top of the modeling isostasy gravimetric map where the approximate circumference of the very probable peak-ring and the very probable rim-crest is highlighted. This information allows to see that the largest island (West Malvinas) would be part of the very probable peak-ring and the smaller island (East Malvinas) would be part of the very probable rim-crest; both separated by the depression that would correspond to the very probable annulus basin. Based on what was analyzed in the Malvinas Islands area, we concluded the Malvinas exhibited geophysics traits of a large ancient asteroid impact; i.e. Malvinas very probable giant impact structure. Very probable impact structure what could be among one of the world's largest impact crater.
Abstract: Clinopyroxene is a key fractionating phase in alkaline magmatic systems, but its impact on metal enrichment processes, and the formation of REE + HFSE mineralisation in particular, is not well understood. To constrain the control of clinopyroxene on REE + HFSE behaviour in sodic (per)alkaline magmas, a series of internally heated pressure vessel experiments was performed to determine clinopyroxene-melt element partitioning systematics. Synthetic tephriphonolite to phonolite compositions were run H2O-saturated at 200?MPa, 650-825?C with oxygen fugacity buffered to log f O2 ? ?QFM + 1 or log f O2 ? ?QFM +5. Clinopyroxene-glass pairs from basanitic to phonolitic fall deposits from Tenerife, Canary Islands, were also measured to complement our experimentally-derived data set. The REE partition coefficients are 0.3-53, typically 2-6, with minima for high-aegirine clinopyroxene. Diopside-rich clinopyroxenes (Aeg5-25) prefer the MREE and have high REE partition coefficients (DEuup to 53, DSmup to 47). As clinopyroxene becomes more Na- and less Ca-rich (Aeg25-50), REE incorporation becomes less favourable, and both the VIM1 and VIIIM2 sites expand (to 0.79 Å and 1.12 Å), increasing DLREE/DMREE. Above Aeg50 both M sites shrink slightly and HREE (VIri? 0.9 Å ? Y) partition strongly onto the VIM1 site, consistent with a reduced charge penalty for REE3+ ? Fe3+ substitution. Our data, complemented with an extensive literature database, constrain an empirical model that predicts trace element partition coefficients between clinopyroxene and silicate melt using only mineral major element compositions, temperature and pressure as input. The model is calibrated for use over a wide compositional range and can be used to interrogate clinopyroxene from a variety of natural systems to determine the trace element concentrations in their source melts, or to forward model the trace element evolution of tholeiitic mafic to evolved peralkaline magmatic systems.
Journal of Volcanology and Geothermal Research, Vol. 398, 106872 17p. Pdf
United States, Hawaii
melting
Abstract: The syneruptive decompression rate of basaltic magma in volcanic conduits is thought to be a critical control on eruptive vigor. Recent efforts have constrained decompression rates using models of diffusive water loss from melt embayments (Lloyd et al. 2014; Ferguson et al. 2016), olivine-hosted melt inclusions (Chen et al. 2013; Le Voyer et al. 2014), and clinopyroxene phenocrysts (Lloyd et al. 2016). However, these techniques are difficult to apply because of the rarity of melt embayments and clinopyroxene phenocrysts suitable for analysis and the complexities associated with modeling water loss from melt inclusions. We are developing a new magma ascent chronometer based on syneruptive diffusive water loss from olivine phenocrysts. We have found water zonation in every olivine phenocryst we have measured, from explosive eruptions of Pavlof, Seguam, Fuego, Cerro Negro and Kilauea volcanoes. Phenocrysts were polished to expose a central plane normal to the crystallographic `b' axis and volatile concentration profiles were measured along `a' and `c' axes by SIMS or nanoSIMS. Profiles are compared to 1D and 3D finite-element models of diffusive water loss from olivine, with or without melt inclusions, whose boundaries are in equilibrium with a melt undergoing closed-system degassing. In every case, we observe faster water diffusion along the `a' axis, consistent with the diffusion anisotropy observed by Kohlstedt and Mackwell (1998) for the so-called `proton-polaron' mechanism of H-transport. Water concentration gradients along `a' match the 1D diffusion model with a diffusivity of 10-10 m2/s (see Plank et al., this meeting), olivine-melt partition coefficient of 0.0007-0.002 (based on melt inclusion-olivine pairs), and decompression rates equal to the best-fit values from melt embayment studies (Lloyd et al. 2014; Ferguson et al. 2016). Agreement between the melt embayment and water-in-olivine ascent chronometers at Fuego, Seguam, and Kilauea Iki demonstrates the potential of this new technique, which can be applied to any olivine-bearing mafic-intermediate eruption using common analytical tools (SIMS and FTIR). In theory, each crystal is a clock, with the potential to record variable ascent in the conduit, over the course of an eruption, and between eruptions.
Earth & Environment Communications, 10.1038/s43247-021-00145-3 16p. Pdf
United States, Hawaii
magmatism
Abstract: Volcanoes represent one of the largest natural sources of metals to the Earth’s surface. Emissions of these metals can have important impacts on the biosphere as pollutants or nutrients. Here we use ground- and drone-based direct measurements to compare the gas and particulate chemistry of the magmatic and lava-seawater interaction (laze) plumes from the 2018 eruption of K?lauea, Hawai’i. We find that the magmatic plume contains abundant volatile metals and metalloids whereas the laze plume is further enriched in copper and seawater components, like chlorine, with volatile metals also elevated above seawater concentrations. Speciation modelling of magmatic gas mixtures highlights the importance of the S2? ligand in highly volatile metal/metalloid degassing at the magmatic vent. In contrast, volatile metal enrichments in the laze plume can be explained by affinity for chloride complexation during late-stage degassing of distal lavas, which is potentially facilitated by the HCl gas formed as seawater boils.
Abstract: Plate tectonics is thought to be a major driver of volatile redistribution on Earth. The budget of nitrogen in Earth's mantle has been suggested to be almost entirely surface-derived. Recycling would contribute nitrogen with relatively heavy 15N/14N isotope ratios to Earth's mantle. This could explain why the Earth's mantle 15N/14N isotope ratio is substantially higher than both solar gases and chondritic parent bodies akin to enstatite chondrites. Here, published nitrogen isotope data of mid-ocean ridge and ocean island basalts are compiled and used to evaluate the nitrogen subduction hypothesis. Nitrogen isotope ratios are used in conjunction with published N2/3He and K2O/TiO2 ratios on the same basalts. Assuming that 3He is not recycled, N2/3He ratios are argued to trace nitrogen addition to mantle sources via subduction. Various mantle source enrichments for basalts are tracked with K2O/TiO2 ratios: elevated K2O/TiO2 ratios are assumed to primarily reflect the contributions of recycled components in the basalts mantle sources. The main result of our data compilation is that for most basalts, ?15N and N2/3He remain constant across a vast range of K2O/TiO2 ratios. Mid-ocean ridge basalts have ?15N signatures that are lower than air by ~4‰ and an average N2/3He ratio of 3.7 (±1.2) x106 (95% confidence, n = 30). Published ?15N and N2/3He are invariant across K2O/TiO2 ratios that vary over a factor of ~20. Using estimates of slab K2O/TiO2 and [TiO2], the observed invariant ?15N and N2/3He may be fit with slabs containing ~0.1 ppm N. A mass balance shows that adding ~10% recycled slabs to the convective mantle only raises the N2/3He by <5%. Lavas from Iceland, Galapagos and Hawaii have high 3He/4He and 15N/14N ratios relative to the convective mantle. Only seven samples show nitrogen isotopic signatures that are unaffected by air contamination, although those samples are poorly characterized for N2/3He. The seven basalts show ?15N between ?2 and 0‰ that do not vary systematically with K2O/TiO2 ratios that vary over a factor of ~5. The N2/3He ratios of these seven basalts is unknown, but the high 3He/4He mantle may be estimated by combining published N2/36Ar to 3He/36Ar ratios. This yields a N2/3He of 2.3 (±1.2) x 106 (1? uncertainty). This is indistinguishable from the MORB estimate of 3.7 (±1.2) x 106. Invariant ?15N across variable degrees of mantle enrichments and MORB-like N2/3He for the high 3He/4He mantle are not consistent with nitrogen addition to plume sources with elevated 3He/4He ratios. A ?15N between ?2 and 0‰ for plume sources, only marginally higher than MORB, could be a primordial feature of undegassed mantle reservoirs. Nonetheless, nitrogen subduction may have contributed to a specific array of mantle sources, as revealed by the few published data on basalts with low 3He/4He ratios. Lavas from the Society plume with low 3He/4He ratios show an enriched mantle source, and they have elevated ?15N ? +0.5‰ and N2/3He > 107. For those, the addition of slabs with concentrations of ~0.1 ppm N to a mantle source can account for the integrated dataset. To summarize, the published data suggest that nitrogen subduction may explain a sub-set of published N isotope data on basalts, but that N recycling has an overall more limited impact on mantle nitrogen than previously thought.
