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The Sheahan Diamond Literature Reference Compilation - Scientific and Media Articles based on Major Keyword - Peridotite
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 Keyword 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 an effort to make it easier for users to track down articles related to a specific topic, KRO has extracted these key words and developed a list of major key words presented in this Key Word Index to which individual key words used in the article reference have been assigned. In most of the individual Key Word Reports the references are in crhonological order, though in some such as Deposits the order is first by key word and then chronological. Only articles classified as "technical" (mainly scientific journal articles) and "media" (independent media articles) are included in the Key Word Index. References that were added in the most recent monthly update are highlighted in yellow.
Peridotite is an ultramafic igneous rock (less than 45% silica) consisting mostly of olivine and pyroxene that compromises most of the earth's upper mantle (to a depth of 400 km). When the oliovine drops below 40% the rock is classified as a pyroxenite. Oceanic plate, about 100 km thick, consists of peridotite except for the upper 6 km or so. Oceanic plate gets subducted back into the mantle, but sometimes it rides over the continental crust (obduction) to form "massifs" that seem out of place. Peridotite classifies into dunite, wehrlite, harzurgite and lherzolite of which lherzolite is dominant. Harzburgite is the source rock most associated with diamond formation, though lherzolite, because of its broad range within the mantle, can also host diamonds. Kimberlites will contain xenoliths of the different types of peridotite.
Petrology of ODP LED 125: mantle peridotites And related rocks from serpentine diapiric seamounts in the IZU-Ogasawara-Mariana forearc
Geological Association of Canada (GAC)/Mineralogical Association of Canada (MAC) Vancouver 90 Program with Abstracts, Held May 16-18, Vol. 15, p. A63. Abstract
Ionov, D.A., Ashchepkov, I.V., Stosch, H.G., et al.
Garnet peridotite xenoliths from the Vitim volcanic field, Baikal region:the nature of the garnet-spinel peridotite transition zone in the continentalmantle.
Journal of Petrology, Vol. 34, No. 6, pp. 1141-1175.
Isotopic disequilibration temperatures (Samarium/neodymium, Rubidium-Strontium) between mineral phases of coarse grained, low temperature garnet peridotites from Kimberley Floors.
Proceedings of Fifth International Kimberlite Conference, Vol. 1, pp. 354-365.
Roy, A., Sarkar, A., Jeyakumar, S., Aggrawal, S.K., Ebihara, M., Satoh, H.
Late Archean mantle metasomatism below eastern Indian craton: evidence from trace elements, REE geochemistry and Sr Nd O isotope systematics of ultramafic dykes.
Proceedings National Academy of Sciences India , Vol. 113, 4, pp. 649-665.
The effect of temperature on the equilibrium distribution of trace elements between clinopyroxene, orthopyroxene, olivine and spinel in upper mantle peridotite.
The effect of temperature on the equilibrium distribution of trace elements between clinopyroxene, orthopyroxene, olivine and spinel in upper mantle peridotite.
Chemical geology, Vol. 221, 1-2, Sept. 5, pp. 65-101.
Polat, A., Herxberg, C., Munker, C., Rodgers, R., Kusky, T., Li, J., Fryer, B.
Geochemical and petrological evidence for a supra subduction zone origin of Neoarchean (ca 2.5 Ga) peridotites, central orogenic belt, North Chin a craton.
Geological Society of America Bulletin, Vol. 118, 7, July pp. 771-784.
Ying, J., Zhang, H., Kita, N., Morishita, Y., Shimoda, G.
Nature and evolution of Late Cretaceous lithospheric mantle beneath the eastern north Chin a craton: constraints from petrology and geochemistry from Junan
Malaspina, N., Hermann, J., Scambelluri, M., Compagnoni, R.
Polyphase inclusions in garnet orthopyroxenite (Dabie Shan, China) as monitors for metasomatism and fluid related trace element transfer in subduction zone.
Geochimica et Cosmochimica Acta, In press available
Zheng-Xue, A.L., Lee, C-T.A., Peslier, A.H., Lenardic, A., Mackwell, S.J.
Water contents in mantle xenoliths from the Colorado Plateau and vicinity: implications for mantle rheology and hydration induced thinning of continental lithosph.
Persistence of mantle lithospheric Re-Os signature during asthenospherization of the subcontinental lithospheric mantle: insights in situ sulphides....
Contributions to Mineralogy and Petrology, Vol. 159, 3, pp. 315-330.
Carbon speciation in the asthenosphere: experimental measurements of the redox conditions at which carbonate bearing melts coexist with graphite or diamond in peridotite assemblages.
Earth and Planetary Science Letters, Vol. 300, 1-2, Nov. 15, pp. 72-84.
Multistage melt fluid peridotite interactions in the refertilized lithospheric mantle beneath the North Chin a craton: constrains from the Li Sr Nd isotopic
Contributions to Mineralogy and Petrology, Vol. 161, 6, pp.
Abstract: The mantle section of Al'Ays ophiolite consists of heterogeneously depleted harzburgites, dunites and large-sized chromitite pods. Two chromitite-bearing sites (Site1 and Site2), about 10 km apart horizontally from one another, were examined for their upper mantle rocks. Cr-spinels from the two sites have different chemistry; Cr-rich in Site1 and Al-rich in Site2. The average Cr-ratio = (Cr/(Cr + Al) atomic ratio) of Cr-spinels in harzburgites, dunites and chromitites is remarkably high 0.78, 0.77 and 0.87, respectively, in Site1, compared with those of Site2 which have intermediate ratio averages 0.5, 0.56 and 0.6, respectively. The platinum-group elements (PGE) in chromitites also show contrasting patterns from Site1 to Site2; having elevated IPGE (Os, Ir, Ru) and strongly depleted in PPGE (Rh, Pt, Pd) with steep negative slopes in the former, and gentle negative slopes in the latter. The oxygen fugacity (?log fO2) values deduced from harzburgites and dunites of Site1 show a wide variation under reducing conditions, mostly below the FMQ buffer. The Site2 harzburgites and dunites, on the other hand are mostly above the FMQ buffer. Two magmatic stages are suggested for the lithospheric evolution of Al'Ays ophiolite in response to a switch of tectonic setting. The first stage produced a peridotites–chromitites suite with Al-rich Cr-spinels, possibly beneath a mid-ocean ridge setting, or most likely in back-arc rift of a supra-subduction zone setting. The second stage involved higher degrees of partial melting, produced a peridotites–chromitites suite with Cr-rich Cr-spinels, possibly in a fore-arc setting. The coexistence of compositionally different mantle suites with different melting histories in a restricted area of an ophiolite complex may be attributable to a mechanically juxtaposed by mantle convection during recycling. The mantle harzburgites and dunites are apt to be compositionally modified during recycling process; being highly depleted (Site1 case) than their original composition (Site2 case).
Economic Geology Research Institute 2015, Vol. 17,, # 1147, 1p. Abstract
China
Peridotite, xenoliths
Abstract: The mantle process during the Early Permian Tarim plume event is revealed by flood basalt and mantle xenoliths. Permian Tarim flood basalts have typical two pulses' eruption. The first pulse of the Tarim flood basalt was erupted at 291-290Ma, characterized by OIB-like Zr/Nb (~5.83), Nb/La and Ce/Pb ratios, and PUM-like initial 187Os/188Os ratios (0.1308-0.1329). They're plotted along a 290±11Ma isochron, implying a pristine "plume mantle" source. The second pulse of the Tarim flood basalt was erupted at 283-281 Ma, with Zr/Nb (~13.6), Nb/La and Ce/Pb ratios similar or close to the lower crust and initial 187Os/188Os ratios (0.1743~19.6740) that deviated from the ~290 Ma isochron line, indicative of significant crustal assimilation. Mantle-derived peridotite and pyroxenite xenoliths hosted in Cenozoic alkali basalts (~20 Ma) are found in the Xikeer, western Tarim Block. Based on their petrographic and geochemical characteristics, peridotite xenoliths can be divided into three groups. Group 1 peridotites, with the presence of the high Mg-number of olivines (91-93) and spinel-pyroxenes clusters, experienced high-degree melt extraction (~17% fractional melting) from garnet- to spinel-stable field. Groups 2 and 3 peridotites, characterized by the clinopyroxenes with spoon-shaped and highly fractionated REE patterns respectively, underwent extensive silicate melt metasomatism at low melt/rock ratios (15) and that the host basanite is incapable of being the metasomatic agent. The Re-Os isotopic systematics of the Xikeer peridotites and pyroxenites yield an isochron of 290±11 Ma, virtually identical to the age of Tarim flood basalts. Their PUM-like Os initial ratios and convecting mantle-like É?Nd(t=290 Ma) strongly suggest that the Xikeer mantle xenoliths derive from the plume mantle. We propose that the Xikeer xenolith suite recorded mantle 'auto-refertilization' process, i.e., they may have been initially formed by melt extraction from the convecting mantle and, shortly after, was refertilized by plume melts during the Early Permian.
Nimis, P., Goncharov, A., Ionov, D.A., McCammon, C.
Fe3 partitioning systematics between orthopyroxene and garnet in mantle peridotite xenoliths and implications for thermobarometry of oxidized and reduced mantle rocks.
Contributions to Mineralogy and Petrology, Vol. 169, 6p.
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.
The Frimingen garnet peridotite ( central Swedish Caledonides). A good example of the characteristic PTt path of a cold mantle wedge garnet peridotite.
The effects of melt depletion and metasomatism on highly siderophile and strongly chalcophile elements: S-Se-Te-Re-PGE systematics of peridotite xenoliths from Kilbourne Hole, New Mexico.
Geochimica et Cosmochimica Acta, Vol. 166, pp. 210-233.
International Geology Review, Vol. 57, 15, pp. 1940-1974.
Technology
Peridotite, experimental petrology
Abstract: Experimental synthesis of spinel peridotite phase assemblages for a range of compositions that mimic natural samples is used to derive a set of empirical geothermometers and geothermobarometers represented by multiple linear regression best-fit surfaces that link the variables of temperature, pressure, and composition. The calibrated geothermometers use reactions that govern the solubility of Al and Cr in both pyroxenes and the Mg–Fe exchange between silicates and spinel. Geothermobarometers map the Mg–Fe exchange between coexisting olivine and clinopyroxene and pyroxenes and Ca–Mg exchange between coexisting pyroxenes. Application of the geothermometers and geothermobarometers to suites of naturally occurring samples indicates that while reactions governing the Cr and Al solubility and solvus of orthopyroxene give useful estimates of ‘original’ mantle temperatures and pressures, respectively, comparable reactions for clinopyroxene yield estimates that are variably dependent on the transport phase of the sample suites. Temperature and pressure estimates from reactions governing Mg and Fe exchange between silicates and spinel and coexisting silicates are all sensitive to the later transport stage of the samples.
Abstract: The Harrat Kishb area of western Saudi Arabia is part of the Cenozoic volcanic fields in the western margin of the Arabian Shield. Numerous fresh ultramafic xenoliths are entrained in the basanite lava of Harrat Kishb, providing an opportunity to study the nature and petrogenetic processes involved in the evolution of the lithospheric mantle beneath the Arabian Shield. Based on the petrological characteristics and mineralogical compositions, the majority of the mantle xenoliths (~ 92%) are peridotites (lherzolites and pyroxene-bearing harzburgites); the remaining xenoliths (~ 8%) are unusual spinel-rich wehrlites containing black Al-spinel micropods. The two types of mantle xenoliths display magmatic protogranular texture. The peridotite xenoliths have high bulk-rock Mg#, high forsterite (Fo90-Fo92) and NiO (0.24-0.46 wt.%) contents of olivine, high clinopyroxene Mg# (0.91-0.93), variable spinel Cr# (0.10-0.49, atomic ratio), and approximately flat chondrite-normalized REE patterns. These features indicate that the peridotite xenoliths represent residues after variable degrees of melt extraction from fertile mantle. The estimated P (9-16 kbar) and T (877-1227 °C) as well as the oxidation state (?logfO2 = ? 3.38 to ? 0.22) under which these peridotite xenoliths originated are consistent with formation conditions similar to most sub-arc abyssal-type peridotites worldwide. The spinel-rich wehrlite xenoliths have an unusual amount (~ 30 vol.%) of Al-spinel as peculiar micropods with very minor Cr2O3 content (< 1 wt.%). Olivines of the spinel-rich wehrlites have low-average Fo (Fo81) and NiO (0.18 wt.%) contents, low-average cpx Mg# (0.79), high average cpx Al2O3 content (8.46 wt.%), and very low-average spinel Cr# (0.01). These features characterize early mantle cumulates from a picritic melt fraction produced by low degrees of partial melting of a garnet-bearing mantle source. The relatively high Na2O and Al2O3 contents of cpx suggest that the spinel-rich wehrlites are formed under high P (11-14 kbar), T (1090-1130 °C), and oxidation state (?logfO2 FMQ = + 0.14 to + 0.37), which occurred slightly below the crust-mantle boundary. The REE patterns of spinel-rich wehrlites are almost similar to those of the associated peridotite xenoliths, which confirm at least a spatial genetic linkage between them. Regarding the formation of Al-spinel micropods in spinel-rich wehrlite cumulates, it is suggested that the melt-rock reaction mechanism is not the only process by which podiform chromitite is formed. Early fractionation of picritic melts produced by partial melting of a mantle source under high P-T conditions could be another mechanism. The cpx composition, not opx, as it was assumed, seems to be the main control of the size and composition of spinel concentrations.
Abstract: Various combinations of diamond, moissanite, zircon, quartz, corundum, rutile, titanite, almandine garnet, kyanite, and andalusite have been recovered from the Dangqiong peridotites. More than 80 grains of diamond have been recovered, most of which are pale yellow to reddish-orange to colorless. The grains are all 100-200 µm in size and mostly anhedral, but with a range of morphologies including elongated, octahedral and subhedral varieties. Their identification was confirmed by a characteristic shift in the Raman spectra between 1325 cm?1 and 1333 cm?1, mostly at 1331.51 cm?1 or 1326.96 cm?1. Integration of the mineralogical, petrological and geochemical data for the Dongqiong peridotites suggests a multi-stage formation for this body and similar ophiolites in the Yarlung-Zangbo suture zone. Chromian spinel grains and perhaps small bodies of chromitite crystallized at various depths in the upper mantle, and encapsulated the UHP, highly reduced and crustal minerals. Some oceanic crustal slabs containing the chromian spinel and their inclusion were later trapped in suprasubduction zones (SSZ), where they were modified by island arc tholeiitic and boninitic magmas, thus changing the chromian spinel compositions and depositing chromitite ores in melt channels.
Contributions to Mineralogy and Petrology, in press available, 17p.
Mantle
Peridotite
Abstract: Natural moissanite (SiC) is reported from mantle-derived samples ranging from lithospheric mantle keel diamonds to serpentinites to podiform chromitites in ophiolites related to suprasubduction zone settings (Luobusa, Dongqiao, Semail, and Ray-Iz). To simulate ultra-reducing conditions and the formation of moissanite, we compiled thermodynamic data for alloys (Fe-Si-C and Fe-Cr), carbides (Fe3C, Fe7C3, SiC), and Fe-silicides; these data were augmented by commonly used thermodynamic data for silicates and oxides. Computed phase diagram sections then constrain the P-T-fO2 conditions of SiC stability in the upper mantle. Our results demonstrate that: Moissanite only occurs at oxygen fugacities 6.5-7.5 log units below the iron-wustite buffer; moissanite and chromite cannot stably coexist; increasing pressure does not lead to the stability of this mineral pair; and silicates that coexist with moissanite have X Mg > 0.99. At upper mantle conditions, chromite reduces to Fe-Cr alloy at fO2 values 3.7-5.3 log units above the moissanite-olivine-(ortho)pyroxene-carbon (graphite or diamond) buffer (MOOC). The occurrence of SiC in chromitites and the absence of domains with almost Fe-free silicates suggest that ultra-reducing conditions allowing for SiC are confined to grain scale microenvironments. In contrast to previous ultra-high-pressure and/or temperature hypotheses for SiC origin, we postulate a low to moderate temperature mechanism, which operates via ultra-reducing fluids. In this model, graphite-/diamond-saturated moderately reducing fluids evolve in chemical isolation from the bulk rock to ultra-reducing methane-dominated fluids by sequestering H2O into hydrous phases (serpentine, brucite, phase A). Carbon isotope compositions of moissanite are consistent with an origin of such fluids from sediments originally rich in organic compounds. Findings of SiC within rocks mostly comprised by hydrous phases (serpentine + brucite) support this model. Both the hydrous phases and the limited diffusive equilibration of SiC with most minerals in the rocks indicate temperatures below 700-800 °C. Moissanite from mantle environments is hence a mineral that does not inform on pressure but on a low to moderate temperature environment involving ultra-reduced fluids. Any mineral in equilibrium with SiC could only contain traces of Fe2+ or Cr3+.
Abstract: Large peridotite massifs are scattered along the 1500?km length of the Yarlung-Zangbo Suture Zone (southern Tibet, China), the major suture between Asia and Greater India. Diamonds occur in the peridotites and chromitites of several massifs, together with an extensive suite of trace phases that indicate extremely low fO2 (SiC, nitrides, carbides, native elements) and/or ultrahigh pressures (UHP) (diamond, TiO2 II, coesite, possible stishovite). New physical and isotopic (C, N) studies of the diamonds indicate that they are natural, crystallized in a disequilibrium, high-T environment, and spent only a short time at mantle temperatures before exhumation and cooling. These constraints are difficult to reconcile with previous models for the history of the diamond-bearing rocks. Possible evidence for metamorphism in or near the upper part of the Transition Zone includes the following: (1) chromite (in disseminated, nodular and massive chromitites) containing exsolved pyroxenes and coesite, suggesting inversion from a high-P polymorph of chromite; (2) microstructural studies suggesting that the chromitites recrystallized from fine-grained, highly deformed mixtures of wadsleyite and an octahedral polymorph of chromite; (3) a new cubic Mg-silicate, with the space group of ringwoodite but an inverse-spinel structure (all Si in octahedral coordination); (4) harzburgites with coarsely vermicular symplectites of opx + Cr-Al spinel ± cpx; reconstructions suggest that these are the breakdown products of majoritic garnets, with estimated minimum pressures to?>?13?GPa. Evidence for a shallow pre-metamorphic origin for the chromitites and peridotites includes the following: (1) trace-element data showing that the chromitites are typical of suprasubduction-zone (SSZ) chromitites formed by magma mixing or mingling, consistent with Hf-isotope data from magmatic (375?Ma) zircons in the chromitites; (2) the composition of the new cubic Mg-silicate, which suggests a low-P origin as antigorite, subsequently dehydrated; (3) the peridotites themselves, which carry the trace element signature of metasomatism in an SSZ environment, a signature that must have been imposed before the incorporation of the UHP and low-fO2 phases. A proposed P-T-t path involves the original formation of chromitites in mantle-wedge harzburgites, subduction of these harzburgites at c. 375?Ma, residence in the upper Transition Zone for >200 Myr, and rapid exhumation at c. 170-150?Ma or 130-120?Ma. Os-isotope data suggest that the subducted mantle consisted of previously depleted subcontinental lithosphere, dragged down by a subducting oceanic slab. Thermomechanical modeling shows that roll-back of a (much later) subducting slab would produce a high-velocity channelized upwelling that could exhume the buoyant harzburgites (and their chromitites) from the Transition Zone in?
Abstract: Continental intraplate basalts (15.42-0.16 Ma) from Abaga-Dalinuoer volcanic field (ADVF) in central Inner Mongolia of eastern China, as a part of Cenozoic volcanic province along eastern margin of the Eurasian continent, provide a good opportunity to explore potential links between deep subduction of the Pacific slab and continental intraplate volcanism. In this study, we report an integrated dataset of whole-rock K-Ar ages, major and trace elements and Sr-Nd-Pb isotopes, and olivine major and minor elements for the Abaga-Dalinuoer basalts (ADBs), and propose that mantle source lithology of the ADB magmas may consist of both pyroxenite and peridotite. The ADBs display low SiO2 (42.3-50.2 wt.%), high MgO (7.3-11.4 wt.%) and moderate K2O + Na2O (3.8-6.4 wt.%), and can be subdivided into basanites, alkali basalts and tholeiitic basalts that are all characterized by ocean island basalt (OIB)-like rare earth elements (REE) and enrichment in both large ion lithosphile elements (LILE) and high field strength elements (HFSE). Olivine phenocrysts have higher Ni and Fe/Mn and lower Mn, Ca and Ca/Fe relative to those from peridotite melts, but exhibit clearly lower Ni contents (< 2500 ppm) compared with expected Ni range (> 3000 ppm) for olivines crystallized from olivine-free pyroxenite melts. Estimated compositions of the ADB primary magmas, together with olivine compositions, suggest an iron-rich mantle source related with silica-deficient pyroxenite that is most likely derived from deeply subducted Pacific oceanic crust. Additionally, peridotite and recent subducted sediments are also required to account for high Ni and MgO in primary magmas together with their trace elements and Sr-Nd-Pb isotope systematics. We suggest that a mixed pyroxenite-peridotite source lithology can better match observed whole-rock and olivine signatures in the ADB, compared with either peridotite only or olivine-free pyroxenite only source lithology. In our model, pyroxenite melts would either react with or mechanically mix with peridotite, and the proportion of pyroxenite melts may range from 30% to 45% for mechanical mixing scenario. A continuous spectrum from tholeiitic to alkali melts revealed by melt-peridotite reaction experiment can explain formation of primary magmas of basanites, alkali basalts and tholeiitic basalts by increasing melting degree of a similar mantle source. Relatively higher 206Pb/204Pb of the ADB may suggest more significant role of recent (< 0.5 Ga) subducted Pacific oceanic materials, in contrast to other Cenozoic basalts in eastern China (e.g., Changbai basalts) that exhibit varying contributions from ancient (> 1.5 Ga) subducted continental sediments. We emphasize that coupled geochemical and geodynamic links (i.e., subduction polarity) between deeply subducted Pacific slab and continental intraplate volcanism in eastern China may exist, which directly support the involvement of deeply subducted Pacific materials in petrogenesis of the ADB. From the perspective of plate motion kinetics, decompression partial melting of upwelling fragmented Pacific slab (silica-deficient pyroxenite + recent subducted sediments) may be triggered by rollback of deeply subducted Pacific slab during Late Cenozoic times. Continental intraplate volcanism in the ADVF generally started with termination of opening of the Japan Sea, suggesting that deep subduction of the Pacific slab may have been an important geodynamic mechanism responsible for tectono-magmatic evolution of northeastern Asia. We suggest that the ADBs have the potential to shed light on genetic links between continental intraplate volcanism and deep subduction of the Pacific slab in geochemical and geodynamic processes.
Abstract: 186Os/188Os variations in mantle peridotites provide constraints on the long-term Pt/Os evolution of the depleted mantle and the Pt/Os ratio of the primitive upper mantle (PUM). We report new 186Os/188Os data for mantle peridotites from continental (Rio Grande Rift and Colorado Plateau) and oceanic (Lena Trough and Hawaiian Islands) settings that span a wide range in fertility (Al2O3 ? 0.67-4.42 wt.%) and 187Os/188Os ratios (0.1138-0.1305). Although peridotite 186Os/188Os values span only a narrow range (from 0.1198345 to 0.1198384), 186Os/188Os broadly correlates with indices of melt depletion including bulk rock Al2O3, spinel Cr#, and clinopyroxene Cr#, consistent with Pt depletion in residual peridotites. PUM 186Os/188Os is estimated to be 0.1198378 ± 23 (2 SD) based on extrapolation of 186Os/188Os-fertility trends, which is very slightly lower than H-chondrites [? 0.1198398 ± 16 (2 SD); Brandon et al., 2006]. This value is consistent with a PUM Pt/Os of 1.7 ± 0.2, similar to average Pt/Os ratios of fertile continental peridotites. The inferred PUM Pt/Os is slightly lower than but within error of Pt/Os values measured in several classes of chondrites [Carbonaceous ? 1.8 ± 0.2, Ordinary ? 1.9 ± 0.1, and Enstatite ? 1.9 ± 0.1 (Brandon et al., 2006)] indicating that PUM Pt/Os is broadly chondritic. In contrast, estimates for PUM Ru/Ir and Pd/Ir (cf. Becker et al., 2006) are suprachondritic. The addition of a chondritic late veneer alone cannot create a combination of chondritic and suprachondritic HSE ratios for the PUM. Instead, minor core segregation occurring concurrently with the addition of a late veneer may explain the observed mantle HSE abundances and ratios. Combined 186Os/188Os-187Os/188Os isotopic and Pt/Os and Re/Os variability in peridotites suggest an average mantle homogenization timescale of ~ 1.2 Ga. In contrast, combined Hf-Nd isotopic and Lu/Hf and Sm/Nd variability in peridotites indicate much shorter homogenization timescales (< 0.4 Ga), potentially reflecting enhanced homogenization by melt-rock interaction to which the Pt-Os and Re-Os systems are relatively immune. The mechanical mixing timescale inferred from Os isotopes is consistent with timescales predicted for whole mantle convection.
Comptes Rendus Geoscience, in press available 11p.
Africa, Morocco
Peridotite
Abstract: The Beni Bousera peridotite contains a diversity of pyroxenite layers. Several studies have postulated that at least some of them represent elongated strips of oceanic lithosphere recycled in the convective mantle. Some pyroxenites were, however, ascribed to igneous crystal segregation or melt-rock reactions. To further constrain the origin of these rocks, we collected 171 samples throughout the massif and examined their variability in relation with the tectono-metamorphic domains. A major finding is that all facies showing clear evidence for a crustal origin are concentrated in a narrow corridor of mylonitized peridotites, along the contact with granulitic country rocks. These peculiar facies were most likely incorporated at the mantle-crust boundary during the orogenic events that culminated in the peridotite exhumation. The other pyroxenites derive from a distinct protolith that was ubiquitous in the massif before its exhumation. They were deeply modified by partial melting and melt-rock reactions associated with lithospheric thinning.
Earth and Planetary Science Letters, Vol. 451, pp. 232-240.
Mantle
Peridotite
Abstract: We present new Zn elemental and isotope data on seventeen fertile and refractory mantle peridotite xenoliths. Eleven fertile peridotites are garnet and spinel lherzolites from Vitim and Tariat (Siberia and Mongolia) and represent some of the most pristine fertile peridotites available. Six refractory peridotites are spinel harzburgites from the Udachnaya kimberlite (Siberian craton) that are nearly pristine residues of high-degree polybaric melting at high pressure (7-4 GPa). Geochemical data suggest that Zn isotopic compositions in the peridotites have not been affected by post-melting processes such as metasomatism, contamination by the host-magmas or alteration. The fertile peridotites have uniform Zn concentrations (59±2 ppm59±2 ppm) and Zn isotopic compositions with ?66Zn (relative to JMC-Lyon-03-0749l)?=?+0.30?±?0.03‰ consistent with the Bulk Silicate Earth estimates of ?66Zn?=?+0.28?±?0.05‰ (Chen et al., 2013). The refractory peridotites have Zn concentrations ranging from 30 to 48 ppm and ?66Zn from +0.10±0.01‰+0.10±0.01‰ to +0.18±0.01‰+0.18±0.01‰ with an average of +0.14±0.03‰+0.14±0.03‰. Our data suggest that the lithospheric mantle has a heterogeneous Zn isotopic composition. Modeling of Zn isotope partitioning during partial melting of fertile mantle suggests that high degrees of melt extraction (>30%) may significantly fractionate Zn isotopes (up to 0.16‰) and that during mantle melting, Zn concentrations and isotopic compositions are mainly controlled by the stability of clinopyroxene and garnet within the melting residue. Because the stability of clinopyroxene and garnet is mainly pressure dependent we suggest that both the depth and the degrees of melt extraction may control Zn isotope fractionation during mantle melting.
Abstract: Olivine is distinguished from all other minerals in providing a remarkable chemical narrative about magmatic processes that occurred in Earth’s crust, mantle, and core over the entire age of Earth history. Olivines in mantle peridotite have Ni contents and Mg numbers that were largely produced by equilibrium crystallization in an early turbulently convecting magma ocean; subsequent stages of partial melting operated to slightly elevate Ni and Mg number in residual olivines. Olivines from Archean komatiites from the Abitibi greenstone belt have Ni contents and Mg numbers that are consistent with an extensively melted peridotite source at great depths in the mantle. Olivines from basaltic oceanic crust, the Icelandic mantle plume and other Phanerozoic occurrences have compositions that record magma chamber crystallization, recharge, mixing, and partial melting. Olivines from the present-day Icelandic mantle plume have compositions that are consistent the melting of a peridotite source; unlike Hawaii, the melting of recycled crust as a distinct pyroxenite lithology is not evident in the olivine chemistry of Iceland. Paleocene picrites from Baffin Island and West Greenland from the ancient Icelandic plume have olivines with Ni contents that are consistent with either Ni-rich peridotite that formed by core-mantle interaction or by low-pressure crystallization of hot and deep magmas. In general, hot magma oceans, mantle plumes, and ambient mantle magmatism form in ways that are captured by the compositions of the olivine crystals that they contain.
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.
Earth and Planetary Science Letters, Vol. 459, pp. 183-195.
Mantle
Peridotite
Abstract: Magmatism at mid ocean ridges is one of the main pathways of S outflux from deep Earth to the surface reservoirs and is a critical step in the global sulfur cycle, yet our understanding of the behavior of sulfide during decompression melting of the upper mantle is incomplete. In order to constrain the sulfur budget of the mantle and reconcile the sulfur and chalcophile element budget of mantle partial melts parental to primitive mid-ocean ridge basalts (MORBs), here we developed a model to describe the behavior of sulfide and Cu during decompression melting by combining the pMELTS thermodynamic model and empirical sulfur contents at sulfide concentration (SCSS) models, taking into account the effect of the presence of Ni and Cu in sulfides on SCSS of mantle-derived melts. Calculation of SCSS along melting adiabat at mantle potential temperature of 1380?°C with variable initial S content in the mantle indicates that the complete consumption or partial survival of sulfide in the melting residue depends on initial S content and degree of melting. Primitive MORBs (Mg# > 60) with S and Cu mostly concentrated in 800-1000 ppm and 80-120 ppm are likely mixture of sulfide undersaturated high degree melts and sulfide saturated low degree melts derived from depleted peridotite containing 100-200 ppm S. Model calculations to capture the effects of variable mantle potential temperatures (1280-1420?°C) indicate that for a given abundance of sulfide in the mantle, hotter mantle consumes sulfide more efficiently than colder mantle owing to the effect of temperature in enhancing sulfide solubility in silicate melt, and higher mantle temperature stabilizing partial melt with higher FeO?FeO? and lower SiO2 and Al2O3, all of which generally enhance sulfide solubility. However, sulfide can still be exhausted by ?10-15%?10-15% melting with bulk S of 100-150 ppm in the mantle when TPTP is as low as 1300?°C. We also show that although variation of View the MathML sourceDCuperidotite/melt and initial Cu in the mantle can all affect the Cu concentration of primitive MORBs, 100-200 ppm S in the MORB source mantle can satisfy both S and Cu geochemistry of partial melts parental to ocean floor basalts.
Geochimica et Cosmochimica Acta, Vol. 200, pp. 232-254.
Mantle
Peridotite
Abstract: Abyssal peridotites are oceanic mantle fragments that were recently processed through ridges and represent residues of both modern and ancient melting. To constrain the nature and timing of melt depletion processes, and the composition of the mantle, we report high-precision Os isotope data for abyssal peridotites from three ocean basins, as well as for Os-rich alloys, primarily from Mesozoic ophiolites. These data are complemented by whole-rock highly siderophile element (HSE: Os, Ir, Ru, Pt, Pd, Re), trace- and major-element abundances for the abyssal peridotites, which are from the Southwest Indian (SWIR), Central Indian (CIR), Mid-Atlantic (MAR) and Gakkel Ridges. The results reveal a limited role for melt refertilization or secondary alteration processes in modifying abyssal peridotite HSE compositions. The abyssal peridotites examined have experienced variable melt depletion (2% to >16%), which occurred >0.5 Ga ago for some samples. Abyssal peridotites typically exhibit low Pd/Ir and, combined with high-degrees of estimated total melt extraction, imply that they were relatively refractory residues prior to incorporation into their present ridge setting. Recent partial melting processes and mid-ocean ridge basalt (MORB) generation therefore played a limited role in the chemical evolution of their precursor mantle domains. The results confirm that many abyssal peridotites are not simple residues of recent MORB source melting, having a more complex and long-lived depletion history. Peridotites from the Gakkel Ridge, SWIR, CIR and MAR indicate that the depleted MORB mantle has 186Os/188Os of 0.1198356 ± 21 (2SD). The Phanerozoic Os-rich alloys yield an average 186Os/188Os within uncertainty of abyssal peridotites (0.1198361 ± 20). Melt depletion trends defined between Os isotopes and melt extraction indices (e.g., Al2O3) allow an estimate of the primitive mantle (PM) composition, using only abyssal peridotites. This yields 187Os/188Os (0.1292 ± 25), and 186Os/188Os of 0.1198388 ± 29, both of which are within uncertainty of previous primitive mantle estimates. The 186Os/188Os composition of the PM is less radiogenic than for some plume-related lavas, with the latter requiring sources with high long-term time-integrated Pt/Os. Estimates of primitive mantle HSE concentrations using abyssal peridotites define chondritic Pd/Ir, which differs from previous supra-chondritic estimates for Pd/Ir based on peridotites from a range of tectonic settings. By contrast, estimates of PM yield supra-chondritic Ru/Ir. The cause of enhanced Ru in the mantle remains enigmatic, but may reflect variable partitioning behavior of Ru at high pressure and temperature.
Geochimica et Cosmochimica Acta, Vol. 200, pp. 167-185.
Africa, South Africa, Russia
Craton, Peridotite
Abstract: We present Mg and Fe isotopic data for whole rocks and separated minerals (olivine, clinopyroxene, orthopyroxene, garnet, and phlogopite) of garnet peridotites that equilibrated at depths of 134-186 km beneath the Kaapvaal and Siberian cratons. There is no clear difference in ?26Mg and ?56Fe of garnet peridotites from these two cratons. ?26Mg of whole rocks varies from ?0.243‰ to ?0.204‰ with an average of ?0.225 ± 0.037‰ (2?, n = 19), and ?56Fe from ?0.038‰ 0.060 with an average of ?0.003 ± 0.068‰ (2?, n = 19). Both values are indistinguishable from the fertile upper mantle, indicating that there is no significant Mg-Fe isotopic difference between the shallow and deep upper mantle. The garnet peridotites from ancient cratons show ?26Mg similar to komatiites and basalts, further suggesting that there is no obvious Mg isotopic fractionation during different degrees of partial melting of deep mantle peridotites and komatiite formation. The precision of the Mg and Fe isotope data (?±0.05‰ for ?26Mg and ?56Fe, 2?) allows us to distinguish inter-mineral isotopic fractionations. Olivines are in equilibrium with opx in terms of Mg and Fe isotopes. Garnets have the lowest ?26Mg and ?56Fe among the coexisting mantle minerals, suggesting the dominant control of crystal structure on the Mg-Fe isotopic compositions of garnets. Elemental compositions and mineralogy suggest that clinopyroxene and garnet were produced by later metasomatic processes as they are not in chemical equilibrium with olivine or orthopyroxene. This is consistent with the isotopic disequilibrium of Mg and Fe isotopes between orthopyroxene/olivine and garnet/clinopyroxene. Combined with one sample showing slightly heavy ?26Mg and much lighter ?56Fe, these disequilibrium features in the garnet peridotites reveal kinetic isotopic fractionation due to Fe-Mg inter-diffusion during reaction between peridotites and percolating melts in the Kaapvaal craton.
Geochimica et Cosmochimica Acta, in press available 49p.
Canada, Nunavut, Somerset Island
peridotite
Abstract: We report detailed petrographic investigations along with 187Os/188Os data in Base Metal Sulfide (BMS) on four cratonic mantle xenoliths from Somerset Island (Rae Craton, Canada). The results shed light on the processes affecting the Re-Os systematics and provide time constraints on the formation and evolution of the cratonic lithospheric mantle beneath the Rae craton. When devoid of alteration, BMS grains mainly consist of pentlandite + pyrrhotite ± chalcopyrite. The relatively high BMS modal abundance of the four investigated xenoliths cannot be reconciled with the residual nature of these peridotites, but requires addition of metasomatic BMS. This is especially evident in the two peridotites with the highest bulk Pd/Ir and Pd/Pt. Metasomatic BMS likely formed during melt/fluid percolation in the Sub Continental Lithospheric Mantle (SCLM) as well as during infiltration of the host kimberlite magma, when djerfisherite crystallized around older Fe-Ni-sulfides. On the whole-rock scale, kimberlite metasomatism is visible in a subset of bulk xenoliths, which defines a Re-Os errorchron that dates the host magma emplacement.
The 187Os/188Os measured in the twenty analysed BMS grains vary from 0.1084 to >0.17 and it shows no systematic variation depending on the sulfide mineralogical assemblage. The largest range in 187Os/188Os is observed in BMS grains from the two xenoliths with the highest Pd/Ir, Pd/Pt, and sulfide modal abundance. The whole-rock TRD ages of these two samples underestimate the melting age obtained from BMS, demonstrating that bulk Re-Os model ages from peridotites with clear evidence of metasomatism should be treated with caution.
The TRD ages determined in BMS grains are clustered around 2.8-2.7, ?2.2 and ?1.9 Ga. The 2.8-2.7 Ga TRD ages document the main SCLM building event in the Rae craton, which is likely related to the formation of the local greenstone belts in a continental rift setting. The Paleoproterozoic TRD ages can be explained by addition of metasomatic BMS during (i) major lithospheric rifting at ?2.2 Ga and (ii) the Taltson-Thelon orogeny at ?1.9 Ga. The data suggest that even metasomatic BMS can inherit 187Os/188Os from their original mantle source. The lack of isotopic equilibration, even at the micro-scale, allowed the preservation of different populations of BMS grains with distinct 187Os/188Os, providing age information on multiple magmatic events that affected the SCLM.
Abstract: The Beni Bousera peridotite contains a diversity of pyroxenite layers. Several studies have postulated that at least some of them represent elongated strips of oceanic lithosphere recycled in the convective mantle. Some pyroxenites were, however, ascribed to igneous crystal segregation or melt–rock reactions. To further constrain the origin of these rocks, we collected 171 samples throughout the massif and examined their variability in relation with the tectono-metamorphic domains. A major finding is that all facies showing clear evidence for a crustal origin are concentrated in a narrow corridor of mylonitized peridotites, along the contact with granulitic country rocks. These peculiar facies were most likely incorporated at the mantle–crust boundary during the orogenic events that culminated in the peridotite exhumation. The other pyroxenites derive from a distinct protolith that was ubiquitous in the massif before its exhumation. They were deeply modified by partial melting and melt–rock reactions associated with lithospheric thinning.
Contributions to Mineralogy and Petrology, Vol. 172, 51-
Mantle
peridotite
Abstract: The fluorine (F) and chlorine (Cl) contents of arc magmas have been used to track the composition of subducted components, and the F and Cl contents of MORB have been used to estimate the halogen content of depleted MORB mantle (DMM). Yet, the F and Cl budget of the Earth’s upper mantle and their distribution in peridotite minerals remain to be constrained. Here, we developed a method to measure low concentrations of halogens (?0.4 µg/g F and ?0.3 µg/g Cl) in minerals by secondary ion mass spectroscopy. We present a comprehensive study of F and Cl in co-existing natural olivine, orthopyroxene, clinopyroxene, and amphibole in seventeen samples from different tectonic settings. We support the hypothesis that F in olivine is controlled by melt polymerization, and that F in pyroxene is controlled by their Na and Al contents, with some effect of melt polymerization. We infer that Cl compatibility ranks as follows: amphibole > clinopyroxene > olivine ~ orthopyroxene, while F compatibility ranks as follows: amphibole > clinopyroxene > orthopyroxene ? olivine, depending on the tectonic context. In addition, we show that F, Cl, Be and B are correlated in pyroxenes and amphibole. F and Cl variations suggest that interaction with slab melts and fluids can significantly alter the halogen content of mantle minerals. In particular, F in oceanic peridotites is mostly hosted in pyroxenes, and proportionally increases in olivine in subduction-related peridotites. The mantle wedge is likely enriched in F compared to un-metasomatized mantle, while Cl is always low (<1 µg/g) in all tectonic settings studied here. The bulk anhydrous peridotite mantle contains 1.4–31 µg/g F and 0.14–0.38 µg/g Cl. The bulk F content of oceanic-like peridotites (2.1–9.4 µg/g) is lower than DMM estimates, consistent with F-rich eclogite in the source of MORB. Furthermore, the bulk Cl budget of all anhydrous peridotites studied here is lower than previous DMM estimates. Our results indicate that nearly all MORB may be somewhat contaminated by seawater-rich material and that the Cl content of DMM could be overestimated. With this study, we demonstrate that the halogen contents of natural peridotite minerals are a unique tool to understand the cycling of halogens, from ridge settings to subduction zones.
Abstract: Subduction of oceanic crust generates chemical and lithological heterogeneities in the mantle. An outstanding question is the extent to which these heterogeneities contribute to subsequent magmas generated by mantle melting, but the answer differs depending on the geochemical behaviour of the elements under investigation: analyses of incompatible elements (those that preferentially concentrate into silicate melts) suggest that recycled oceanic crust is an important contributor, whereas analyses of compatible elements (those that concentrate in crystalline residues) generally suggest it is not. Recently, however, the concentrations of Mn and Ni—two elements of varying compatibility—in early-crystallizing olivines, have been used to infer that erupted magmas are mixtures of partial melts of olivine-rich mantle rocks (that is, peridotite) and of metasomatic pyroxene-rich mantle rocks (that is, pyroxenite) formed by interaction between partial melts of recycled oceanic crust and peridotite. Here, we test whether melting of peridotite alone can explain the observed trend in olivine compositions by combining new experimental data on the partitioning of Mn between olivine and silicate melt under conditions relevant to basalt petrogenesis with earlier results on Ni partitioning. We show that the observed olivine compositions are consistent with melts of fertile peridotite at various pressures—importantly, melts from metasomatic pyroxenites are not required. Thus, although recycled materials may well be present in the mantle source regions of some basalts, the Mn and Ni data can be explained without such a contribution. Furthermore, the success of modelling the Mn–Ni contents of olivine phenocrysts as low-pressure crystallization products of partial melts of peridotite over a range of pressures implies a simple new approach for constraining depths of mantle melting.
Hydrogen of the lithospheric mantle in the northern Slave craton ( Canada): constraints from combined FTIR and EBSD measurements on peridoite xenoliths.
Abstract: How the Earth's continental crust was formed in the Hadean eon is a subject of considerable debates [1-4]. For example, shallow hydrous peridotites [2,5], in particular the Hadean Earth's serpentinites [6], are potentially important ingredients in the creation of the continental ptoto-crust, but the mechanisms of this formation remain elusive. In this work, experiments to explore serpentinite-basalt interaction under conditions of the Hadean Earth were conducted. Kinetic runs lasting 0.5 to 48 hours at 0.2 to 1.0 GPa and 1250 to 1300°C reveal dehydration of serpentinite and release of a Si-Al-Na-K-rich aqueous fluid. For the first time, generation of heterogeneous hydrous silicic melts (56 to 67 wt% SiO2) in response to the fluid-assisted fertilisation and the subsequent partial melting of the dehydrated serpentinite has been discovered. The melts produced at 0.2 GPa have compositions similar to those of the bulk continental crust [2,3]. These new findings imply that the Earth's sialic proto-crust may be generated via fluid-assisted melting of serpentinized peridotite at shallow depths (?7 km) that do not require plate subduction during the Hadean eon. Shallow serpentinite dehydration and melting may be the principal physico-chemical processes affecting the earliest lithosphere.
Making Earth's continental crust from serpentinite and basalt.
Earth and Planetary Science Letters, Vol. 475, pp. 143-151.
Africa
peridotites
Abstract: Continental Flood Basalts (CFB) result from voluminous outpourings of magma that often precede continental break-up. Notwithstanding the petrogenetic importance of CFBs, the nature of the mantle source for such magmas is contentious, particularly with regard to picrites with Ni-rich olivine phenocrysts. Previous studies have suggested that Ni-rich olivines associated with plume volcanism in regions of thickened (>90 km) lithosphere are related to either source mineralogy differences (peridotite versus pyroxenite) or change in olivine-melt partitioning due to pressure increase. In order to evaluate these two hypotheses, we present trace element data for olivines from the Karoo CFB Tuli and Mwenezi picrites and the Etendeka CFB Horingbaai/LTZ-L type picrites, all of which erupted in regions of thickened (>90 km) lithosphere in southern Africa. Karoo picrite olivines are Ni-rich, Ca- and Mn-poor, and have low (<1.4) 100*Mn/Fe. These compositions are consistent with a pyroxenitic source. Etendeka Horingbaai/LTZ-L picrite olivines do not show Ni-enrichment, but are characterized by high Al and Cr, and high (>1.4) 100*Mn/Fe, which is more consistent with high temperature melting of a dominantly peridotitic source. We also show that the Karoo and Etendeka olivines are characterized by distinct Mn/Zn ratios of <13 and >15, respectively.In addition, bulk rock geochemical data compilations and previously reported olivine for Karoo and Etendeka CFBs are discussed in order to further constrain source components based on previously described pyroxenite melt geochemical indices such as MgO-CaO systematics, FeO/MnO, Zn/Fe, and FC3MS (FeO/CaO-3*MgO/SiO2). These geochemical indices suggest a pyroxenite-dominated source for Karoo CFBs as well as for Etendeka ferropicrites whereas a peridotite-dominated source is indicated for Etendeka Horingbaai/LTZ-L type picrites analyzed in this study. Based on our data, Ni-enrichment of olivine in plume-related magmas in regions of thickened lithosphere in southern Africa is not ubiquitous. We therefore suggest that mineralogical variation of the source is a more likely major control of olivine chemistry and parent melt variations for Karoo and Etendeka CFBs. We also show that olivine Mn-Zn correlations are a useful discriminator for source variation and recommend the use of olivine for a pyroxenite-dominated source relative to olivine for a peridotite-dominated source.
Earth and Planetary Science Letters, Vol. 474, pp. 128-137.
Mantle
peridotites
Abstract: To better constrain the Ca isotopic composition of the Bulk Silicate Earth (BSE) and explore the Ca isotope fractionation in the mantle, we determined the Ca isotopic composition of 28 peridotite xenoliths from Mongolia, southern Siberia and the Siberian craton. The samples are divided in three chemical groups: (1) fertile, unmetasomatized lherzolites (3.7-4.7 wt.% Al2O3); (2) moderately melt-depleted peridotites (1.3-3.0 wt.% Al2O3) with no or very limited metasomatism (LREE-depleted cpx); (3) strongly metasomatized peridotites (LREE-enriched cpx and bulk rock) further divided in subgroups 3a (harzburgites, 0.1-1.0% Al2O3) and 3b (fertile lherzolites, 3.9-4.3% Al2O3). In Group 1, ?44/40Ca of fertile spinel and garnet peridotites, which experienced little or no melting and metasomatism, show a limited variation from 0.90 to 0.99‰ (relative to SRM 915a) and an average of 0.94 ± 0.05‰ (2SD, ), which defines the Ca isotopic composition of the BSE. In Group 2, the ?44/40Ca is the highest for three rocks with the lowest Al2O3, i.e. the greatest melt extraction degrees (average ‰, i.e. ?0.1‰ heavier than the BSE estimate). Simple modeling of modal melting shows that partial melting of the BSE with ranging from 0.10 to 0.25 can explain the Group 2 data. By contrast, ?44/40Ca in eight out of nine metasomatized Group 3 peridotites are lower than the BSE estimate. The Group 3a harzburgites show the greatest ?44/40Ca variation range (0.25-0.96‰), with ?44/40Ca positively correlated with CaO and negatively correlated with Ce/Eu. Chemical evidence suggests that the residual, melt-depleted, low-Ca protoliths of the Group 3a harzburgites were metasomatized, likely by carbonate-rich melts/fluids. We argue that such fluids may have low (?0.25‰) ?44/40Ca either because they contain recycled crustal components or because Ca isotopes, similar to trace elements and their ratios, may be fractionated by kinetic and/or chromatographic effects of melt percolation in the mantle. The ?44/40Ca in Group 3b lherzolites (0.83-0.89‰) are lower than in the BSE as well, but the effects of metasomatism on ?44/40Ca are smaller, possibly because of the high Ca contents in their protoliths and/or smaller ?44/40Ca differences between the protoliths and metasomatic agents. The BSE estimates based on fertile peridotites in this study fall in the ?44/40Ca ranges for oceanic and continental basalts, various meteorites (achondrites; carbonaceous, ordinary and enstatite chondrites), Mars, and the Moon. These results provide benchmarks for the application of Ca isotopes to planet formation, mantle evolution, and crustal recycling.
Doklady Earth Sciences, Vol. 476, 1, pp. 1058-1061.
Mantle
peridotite
Abstract: Deformed orthopyroxene grains are studied in detail in mantle peridotite. It is shown that deformation of enstatite is accompanied by its decomposition with the formation of low-temperature phases (pargasite, Fe-rich olivine) and restite represented by depleted enstatite, forsterite, and small newly formed chrome spinellide grains. The role of plastic deformation in initiation of partial melting of peridotite and in the formation new chrome spinellide grains is discussed.
Abstract: Mantle metasomatism by percolating melts/fluids can significantly modify the geochemical and mineralogical compositions of the sub-continental lithospheric mantle (SCLM). We present a detailed study of water contents and Li concentrations and isotopic compositions in mantle minerals from a suite of peridotite xenoliths entrained by a Cenozoic Strombolian volcano in the southern French Massif Central (FMC). Wide ranging clinopyroxene trace element distributions (e.g., (La/Yb)N from 0.25 to 22.21; Ti/Eu ratios from 453 to 4892) suggest that the SCLM has undergone metasomatism by carbonatitic melts/fluids or melts/fluids related to subducted materials. Two amphibole-bearing samples exhibit depletion of light rare earth elements (LREE; (La/Yb)N = 0.26 and 0.30, respectively) in amphiboles, similar to that in co-existing clinopyroxenes; these samples indicate that amphiboles grew during a separate modally metasomatic event predating the cryptic metasomatism accounting for LREE enrichment and negative HFSE anomalies in other samples. Mineral Li concentrations are similar to those in the normal mantle, with inter-mineral Li partitioning nearly equilibrated and intragranular Li distributions nearly homogeneous. However, negative ?7Li values of pyroxenes in some samples (as low as ? 8.8‰ in clinopyroxene of sample MC38) can be attributed to diffusive exchange with a small-volume melt of moderate Li concentration and light Li isotopic composition, originally associated with a recycled component. Preservation of the currently observed large inter-mineral Li isotopic variations indicates that melt percolation occurred shortly before entrainment of the peridotite xenoliths by the host magma. Mineral water contents vary from 41 to 428 ppm in clinopyroxenes and from 28 to 152 ppm in orthopyroxenes, and their roughly negative co-variation with coexisting olivine Fo contents imply that partial melting was the main control over mineral water content variations in most samples. Varied water contents in LREE-enriched metasomatized samples indicate the involvement of metasomatic agents of different origins. The aqueous agent responsible for generation of amphiboles in two samples did not produce a notable increase in the water contents of coexisting nominally anhydrous minerals.
Abstract: Diamond nucleation and growth were investigated experimentally at 7.5 and 10.5?GPa and temperatures up to 1500?°C. Samples consisted of two layers: i) H2O- and CO2-bearing model sediment and ii) graphite-bearing garnet harzburgite comprising natural minerals. Two experimental series were conducted, one under a controlled temperature gradient with the sedimentary layer usually in the cold zone and the other under isothermal conditions. In the latter case, diamond seeds were added to the sedimentary mixture. During the experiments, the sedimentary layer partially or completely melted, with the melt percolating and interacting with the adjacent harzburgite. The graphite-to-diamond transition in the peridotite was observed above 1300?°C at 7.5?GPa and 1200?°C at 10.5?GPa in the temperature-gradient experiments, and at temperatures ~100?°C lower in the isothermal experiments with diamond seeds. Newly formed diamond occurs mostly as individual grains up to 10??m in size and is separate from graphite aggregates. In some cases, an association of diamond with magnesite was observed. Diamond nucleation occurs in hydrous and CO2-bearing silicate melt following graphite dissolution and recrystallization. In the case of the diamond-magnesite association, diamond was probably formed through carbonate reduction coupled with graphite oxidation. The composition of the melts ranged from “carbonatitic” with ~10?wt% SiO2 and?>?50?wt% volatiles to hydrous silicate with ~40?wt% SiO2 and?
Abstract: An important issue in Earth’s earliest history is the timing and mixing history of the late accreted material that supplied highly siderophile elements to Earth’s mantle after core segregation. Previously, constraints on ancient mantle processes could only be obtained indirectly from mantle-derived magmas such as basalts or komatiites. Relics of Eoarchean (older than 3.8 Ga) mantle were proposed to occur within the Eoarchean terrains of western Greenland. Here we provide geochemical evidence, including combined platinum group element (PGE) and Re-Os isotope data, showing that modern mantle-like peridotites occur at two localities in southwest Greenland. Rhenium-depletion model ages of these peridotites are mostly of Eoarchean age, in accord with U-Pb zircon ages of crosscutting granitoid intrusives. PGE abundances and patterns are similar to those of modern depleted mantle peridotites. For the first time, such patterns provide conclusive evidence for preservation of Eoarchean depleted mantle rocks that are clearly distinguishable from magmatic cumulates or komatiites. Abundances of Os, Ir, and Ru combined with Os isotope compositions in the Greenland peridotites reveal that primitive late accreted material appears to have been efficiently mixed into the sampled mantle domains by Eoarchean time.
Earth and Planetary Science Letters, Vol. 494, pp. 172-189.
Mantle
peridotites
Abstract: The oxygen fugacity (fO2) of the oceanic upper mantle has fundamental implications for the production of magmas and evolution of the Earth's interior and exterior. Mid-ocean ridge basalts and peridotites sample the oceanic upper mantle, and retain a record of oxygen fugacity. While fO2 has been calculated for mid-ocean ridge basalts worldwide (>200 locations), ridge peridotites have been comparatively less well studied (33 samples from 11 locations), and never in the same geographic location as basalts. In order to determine whether peridotites and basalts from mid-ocean ridges record congruent information about the fO2 of the Earth's interior, we analyzed 31 basalts and 41 peridotites from the Oblique Segment of the Southwest Indian Ridge. By measuring basalts and peridotites from the same ridge segment, we can compare samples with maximally similar petrogenetic histories. We project the composition and oxygen fugacity of each lithology back to source conditions, and evaluate the effects of factors such as subsolidus diffusion in peridotites and fractional crystallization in basalts. We find that, on average, basalts and peridotites from the Oblique Segment both reflect a source mantle very near the quartz-fayalite-magnetite (QFM) buffer. However, peridotites record a significantly wider range of values (nearly 3 orders of magnitude in fO2), with a single dredge recording a range in fO2 greater than that previously reported for mid-ocean ridge peridotites worldwide. This suggests that mantle fO2 may be heterogeneous on relatively short length scales, and that this heterogeneity may be obscured within aggregated basalt melts. We further suggest that the global peridotite fO2 dataset may not provide a representative sample of average basalt-source mantle. Our study motivates further investigation of the fO2 recorded by ridge peridotites, as peridotites record information about the fO2 of the Earth's interior that cannot be gleaned from analysis of basalts alone.
Geochemistry, Geophysics, Geosystems, Vol. 19, 3, pp. 595-620.
Mantle
peridotites
Abstract: We present phase equilibria experiments on a depleted peridotite (Mg# 92) fluxed with variable proportions of a slab?derived rhyolitic melt (with 9.4 wt.% H2O, 5 wt.% CO2), envisaging an interaction that could occur during formation of continents by imbrication of slabs/accretion of subarc mantles. Experiments were performed with 5 wt.% (Bulk 2) and 10 wt.% (Bulk 1) melt at 950-1175°C and 2-4 GPa using a piston?cylinder and a multi?anvil apparatus, to test the hypothesis that volatile?bearing mineral?phases produced during craton formation can cause reduction in aggregate shear?wave velocities (VS) at mid?lithospheric depths beneath continents. In addition to the presence of olivine, orthopyroxene, clinopyroxene, and garnet/spinel, phlogopite (Bulk 1: 3-7.6 wt.%; Bulk 2: 2.6-5 wt.%) at 2-4 GPa, and amphibole (Bulk 1: 3-9 wt.%; Bulk 2: 2-6 wt.%) at 2-3 GPa (?1050°C) are also present. Magnesite (Bulk 1: ?1 wt.% and Bulk 2: ?0.6 wt.%) is present at 2-4 GPa (<1000°C at 3 and?100 km depth.
Abstract: Peridotites dredged from mid-ocean ridges and glassy mid-ocean ridge basalts (MORB) transmit information about the oxygen fugacity (fO2) of Earth's convecting upper mantle to the surface. Equilibrium assemblages of olivine+orthopyroxene+spinel in abyssal peridotites and Fe3+/?Fe ratios in MORB glasses measured by X-ray absorption near-edge structure (XANES) provide independent estimates of MORB source region fO2, with the former recording fO2 approximately 0.8 log units lower than the latter relative to the quartz-fayalite-magnetite (QFM) buffer. To test cross-compatibility of these oxybarometers and examine the compositional effects of changing fO2 on a peridotite plus melt system over a range of Earth-relevant fO2, we performed a series of experiments at 0.1 MPa and fO2 controlled by CO-CO2 gas mixes between QFM-1.87 and QFM+2.23 in a system containing basaltic andesite melt saturated in olivine, orthopyroxene, and spinel. Oxygen fugacities recorded by each method are in agreement with each other and with the fO2 measured in the furnace. Measurements of fO2 from the two oxybarometers agree to within 1? in all experiments. These results demonstrate that the two methods are directly comparable and differences between fO2 measured in abyssal peridotites and MORB result from geographic sampling bias, petrological processes that change fO2 in these samples after separation of melts and residues, or abyssal peridotites may not be residues of MORB melting. As fO2 increases, spinel Fe3+ concentrations increase only at the expense of Cr from QFM-1.87 to QFM-0.11. Above QFM, Al is also diluted in spinel as the cation proportion of Fe3+ increases. None of the three spinel models tested, MELTS (Ghiorso and Sack 1995), SPINMELT (Ariskin and Nikolaev 1996), and MELT_CHROMITE (Poustovetov and Roeder 2001), describe these compositional effects, and we demonstrate that MELTS predicts residues that are too oxidized by >1 log unit to have equilibrated with the coexisting liquid phase. Spinels generated in this study can be used to improve future thermodynamic models needed to predict compositional changes in spinels caused by partial melting of peridotites in the mantle or by metamorphic reactions as peridotites cool in the lithosphere. In our experimental series, where the ratio of Fe2O3/FeO in the melt varies while other melt compositional parameters remain nearly constant, experimental melt fraction remains constant, and Fe3+ becomes increasingly compatible in spinel as fO2 increases. Instead of promoting melting, increasing the bulk Fe3+/?Fe ratio in peridotite drives reactions analogous to the fayalite-ferrosilite-magnetite reaction. This may partly explain the absence of correlation between Na2O and Fe2O3 in fractionation-corrected MORB.
Journal of Asian Earth Sciences, Vol. 164, pp. 179-193.
Asia, Myanmar
peridotites
Abstract: Peridotites from the Myitkyina ophiolite are mainly composed of lherzolite and harzburgite. The lherzolites have relatively fertile compositions, with 39.40-43.40?wt% MgO, 1.90-3.17?wt% Al2O3 and 1.75-2.84?wt% CaO. They contain spinel and olivine with lower Cr# (12.6-18.2) and Fo values (88.7-91.6) than those of the harzburgites (24.5-59.7 and 89.6-91.6 respectively). The harzburgites have more refractory compositions, containing 42.40-46.23?wt% MgO, 0.50-1.64?wt% Al2O3 and 0.40-1.92?wt% CaO. PGE contents of the peridotites show an affinity to the residual mantle. Evaluation of petrological and geochemical characteristics of these peridotites suggests that the lherzolites and harzburgites represent residual mantle after low to moderate degrees of partial melting, respectively, in the spinel stability field. The U-shaped, primitive mantle-normalized REE patterns and strong positive Ta and Pb anomalies of the harzburgites suggest melt/fluid refertilization in either a MOR or SSZ setting after their formation at a MOR. Mineral separation of the peridotites has yield a range of exotic minerals, including diamond, moissanite, native Si, rutile and zircon, a collection similar to that reported for ophiolites of Tibet and the Polar Urals. The discovery of these exotic minerals in the Myitkyina ophiolite supports the view that they occur widely in the upper oceanic mantle.
Earth and Planetary Science Letters, Vol. 494, 1, pp. 50-59.
Mantle
peridotites
Abstract: Elevated abundances of highly siderophile elements in Earth's mantle are thought to reflect the late accretion of primitive material after the cessation of core formation, but the origin of this material, and whether or not it can be linked to specific types of meteorites remain debated. Here, mass-dependent Ru isotopic data for chondrites and terrestrial peridotites are reported to evaluate the chemical nature and type of the late-accreted material. After correction for nucleosynthetic Ru isotope anomalies, enstatite, ordinary and carbonaceous chondrites all have indistinguishable mass-dependent Ru isotopic compositions. Thus, neither distinct formation conditions in the solar nebula nor parent body processes resulted in significant mass-dependent Ru isotope fractionation. All five terrestrial peridotites analyzed have mass-dependent Ru isotopic compositions that are indistinguishable from each other and from the composition of chondrites. The chondritic mass-dependent Ru isotopic composition of Earth's mantle is difficult to reconcile with prior suggestions that the late accretionary assemblage was a mixture of chondrites with a chemically evolved metal component. Although this mixture can reproduce the suprachondritic Ru/Ir inferred for Earth's mantle, it consistently predicts a heavy Ru isotopic composition of Earth's mantle with respect to chondrites. This is because metal components with elevated Ru/Ir are also enriched in heavy Ru isotopes, resulting from isotope fractionation during core crystallization. Thus, if late accretion involved impacts of differentiated protoplanetary bodies, then the projectile cores must have been either homogenized upon impact, or added to Earth's mantle completely, because otherwise Earth's mantle would have inherited a non-chondritic mass-dependent Ru isotopic composition from the unrepresentative sampling of core material.
Earth and Planetary Science Letters, Vol. 498, pp. 427-435.
Mantle
peridotites
Abstract: Geochemical studies of mid-ocean-ridge basalts (MORB) and mantle peridotites (e.g., abyssal peridotites) provide independent constraints on the composition and evolution of the convecting mantle. Recent studies have revealed systematic differences in the radiogenic isotope compositions of MORB and abyssal peridotites that call into question the complementary nature of these two windows to the upper mantle. The origin of these differences is fundamental to our understanding of MORB petrogenesis and the composition and depletion history of the upper mantle. The use of isotope variations in basalts to probe the composition and evolution of the mantle is predicated on the assumption of local (i.e., grain-scale) isotopic equilibrium during mantle melting. However, several studies have reported Os- and Pb-isotope disequilibrium in distinct populations of peridotite-derived sulfides, with sulfides included within silicate grains typically possessing more “depleted” isotopic compositions than interstitial sulfides. In principle, grain-scale isotopic heterogeneity could reflect variable radiogenic ingrowth in ancient sulfides with variable parent/daughter ratios, or partial re-equilibration of low-Re/Os and U/Pb sulfides with more radiogenic silicate phases along grain boundaries during mantle melting. This would require that sulfides fail to maintain isotopic equilibrium with neighboring phases over geologically long (? Ga) time scales. The preservation of Os-isotope disequilibrium in peridotites has been ascribed in several studies to the armoring effect of low-[Os] silicates, which limits diffusive exchange between isolated Os-rich sulfides. This raises the prospect that peridotite-derived melts may not inherit the Os- (or Pb-) isotope composition of their source, which could account for the recently documented systematic differences in the Os- and Pb-isotope compositions of MORB and mantle peridotites. Although the preservation of isotopic heterogeneity in mantle sulfides is commonly ascribed to the above “armoring effect”, the diffusive equilibration timescale of spatially separated sulfides in mantle peridotites has not previously been rigorously estimated. This study examines the parameters that control this equilibration timescale (average sulfide size and spacing, Os and Pb diffusivity in armoring silicate minerals, and element partitioning between silicate and sulfide phases). Equilibration timescale estimates using available constraints on these parameters reveal that most mantle sulfides are expected to isotopically re-equilibrate with neighboring sulfides in less than a few 10 s of Myr at convecting mantle temperatures. Maintenance of isotopic disequilibrium over the ? Ga timescales suggested by observed intra-sample Os- and Pb-isotope heterogeneity requires very large sulfides (>100 ?m) separated by several mm or diffusion rates (D <10?18 m2/s), slower than for most elements in olivine. Combined with the observation of intra-sample major element heterogeneity in sulfide Ni and Fe abundances (which should equilibrate quickly in the convecting mantle), these results suggest that the observed isotopic disequilibrium is unlikely to be an ancient feature in mantle peridotites. Instead, recent sulfide metasomatism linked to interaction with melts derived from isotopically enriched eclogite or pyroxenite (or fertile and/or metasomatized peridotite) components is a more likely explanation for observed intra-sample isotopic heterogeneity in peridotites. This interpretation is also consistent with systematic differences between the Nd- and Hf-isotope compositions of MORB and abyssal peridotites. These results further strengthen the proposal that MORB do not accurately reflect the average isotopic composition of the convecting upper mantle, and that upper mantle peridotite is, on average, significantly more depleted and refractory than suggested by MORB-based estimates. The effects of melt generation in a heterogeneous marble-cake mantle need to be explicitly considered when using basalt compositions to constrain mantle composition and evolution.
Abstract: The Re-Os isotope system is well suited to constraining the timing of melt depletion of Archean mantle peridotites. In contrast, the variability inherent in post-Archean mantle Os isotope evolution leads to increasing uncertainty in Re-Os model ages. The Lu-Hf isotopic system has shown some potential for dating peridotite formation ages, providing valuable ages that are complementary to the Re-Os system. For post-Archean mantle peridotites, the key target in the Lu-Hf isotopic work is clinopyroxene (Cpx), because of its high Lu and Hf concentrations and the typical absence of garnet in these rocks. However, orthopyroxene (Opx) can contrain 20% or more of the Hf budget of spinel peridotites and somethimes over 40% of the Lu budget, with Lu/Hf ratios 3-4 times those of Cpx. Thus, Opx Lu-Hf isotopic compositions cannot be ignored or simply calculated, as the equilibrium temperatures of mantle peridotites prior to eruption could be lower or higher than the Hf closure temperature (Tc(Hf)~900ºC). Here we explore Lu-Hf partitioning in spinel peridotite xenoliths from the Cameroon Volcanic Line in additin to WR Re-Os analyses. The Hf isotopic composition of Opx in these rocks is equal to or higher than that of Cpx, consistent with some samples having equilibrium temperatures close to Tc(Hf). Combining Cpx and Opx, the constructed WR Lu-Hf isochron yields an age of 2.01±0.36 Ga (2?; MSWD = 11.4; ?Hfi = -0.8±19.2), which is in accordance with the oldest of the variable Re-Os model ages. The continental sector of the Cameroon Line runs close to the edge of the Congo craton. The Hf-Os data indicate that the lithosphere underpinning this region formed in the Paleoproterozoic (~2Ga) most likely during the Paleoproterzoic assembly between the Congo and West African Cratons. We emphasize that Opx and Cpx should be combined together to construct the WR isochron in order to obtain the precise age and initial Hf isotope compositions of post-Archean spinel peridotites.
Abstract: The H/C ratio in earth’s exosphere is higher than it is in the source region of primitive basalts, suggesting an enriched carbon reservoir in the mantle[1]. A plausible explanation is that subduction of carbon may have enriched the mantle in recycled carbon over time. Average basaltic crust contains ~ 2 wt.% CO2 [2], and modeling of slab devolatilisation suggests that subducted carbonate may survive to be transported deeper into the mantle [3]. Carbonated oceanic crust should melt in the transition zone along most subduction geotherms due to a deep trough in the carbonated basalt solidus, and mineral inclusions in superdeep diamonds testify to carbonate melt in their formation [4]. Along cool subduction geotherms carbonate may subduct into the lower mantle, potentially enriching the deep mantle in carbon. Here we report on laser-heated diamond anvil cell experiments in the CaO-MgO-SiO2-CO2 and FeO-MgO-SiO2-CO2 systems at lower mantle pressures where we investigate the stability of carbonate in oceanic crust, and test for decarbonation and diamond forming reactions involving carbonate and coexisiting free silica. We find that carbonate reacts with silica to form bridgmanite ± Ca-perovskite + CO2 at pressures in the range of ~50 to 70 GPa. These decarbonation reactions form an impenetrable barrier to subduction of carbonate into the deeper lower mantle, however, slabs may carry solid CO2 (Phase V) into the deeper lower mantle. We also identify reactions where carbonate or CO2 dissociate to form diamond plus oxygen. We suggest that the deep lower mantle may become enriched in carbon in the form of diamond over time due to subduction of carbonate and solid CO2 and its eventual dissociation to form diamond plus oxygen. Release of oxygen during diamond formation may also provide a mechanism for locally oxidizing the deep mantle.
Abstract: Peridotites occur as lensoid bodies within the Mesoarchaean orthogneiss in the Akia terrane of Southern West Greenland. The Ulamertoq peridotite body is the largest of these peridotites hosted within the regional orthogneiss. It consists mainly of olivine, orthopyroxene, and amphibole-rich ultramafic rocks exhibiting metamorphic textural and chemical features. Chromitite layers from different localities in Ulamertoq show contrasting characteristics. In one locality, zoned chromites are hosted in orthopyroxene-amphibole peridotites. Compositional zonation in chromites is evident with decreasing Cr and Fe content from core to rim, while Al and Mg increase. Homogeneous chromites from another locality are fairly uniform and Fe-rich. The mineral chemistry of the major and accessory phases shows metamorphic signatures. Inferred temperature conditions suggest that the zoned chromites, homogeneous chromites, and their hosts are equilibrated at different metamorphic conditions. In this paper, various mechanisms during the cumulus to subsolidus stages are explored in order to understand the origin of the two contrasting types of chromites.
Geostandards and Geoanalytical Research, doi:10.111/ggr.12240
Global
peridotite
Abstract: A rapid sample preparation procedure is described to determine trace element compositions of peridotites using LA?ICP?MS. Peridotite powders were fused with albite in a molybdenum?graphite assembly to obtain homogeneous glasses. Best conditions for the fusion procedure (heating at 1500 to 1550 °C for 10 to 15 min with a sample?to?flux ratio of 1:2) were constrained with melting experiments on two USGS reference materials, PCC?1 and DTS?2B. Mass fractions of first series transition elements, Ba and Pb in quenched glasses of PCC?1 and DTS?2B are consistent with published data within 10% RSD. Three spinel peridotite xenoliths from eastern China were analysed following both our method and conventional solution ICP?MS. Compared with solution ICP?MS, the relative deviations of our method for most elements were within 10%, while for the REE, Ta, Pb, Th and U, were within 20%. In particular, volatile elements (e.g., Pb and Zn) are retained in the glass. Compared with conventional wet chemistry digestion, our method is faster. Additional advantages are complete sample fusion, especially useful for samples with acid?resistant minerals (spinel, rutile), and long?term conservation of glasses allowing unlimited repeated measurements with micro?beam techniques. The same approach can be used for analyses of other mantle rocks, such as eclogites and pyroxenites.
Abstract: Peridotites occur as lensoid bodies within the Mesoarchaean orthogneiss in the Akia terrane of Southern West Greenland. The Ulamertoq peridotite body is the largest of these peridotites hosted within the regional orthogneiss. It consists mainly of olivine, orthopyroxene, and amphibole-rich ultramafic rocks exhibiting metamorphic textural and chemical features. Chromitite layers from different localities in Ulamertoq show contrasting characteristics. In one locality, zoned chromites are hosted in orthopyroxene-amphibole peridotites. Compositional zonation in chromites is evident with decreasing Cr and Fe content from core to rim, while Al and Mg increase. Homogeneous chromites from another locality are fairly uniform and Fe-rich. The mineral chemistry of the major and accessory phases shows metamorphic signatures. Inferred temperature conditions suggest that the zoned chromites, homogeneous chromites, and their hosts are equilibrated at different metamorphic conditions. In this paper, various mechanisms during the cumulus to subsolidus stages are explored in order to understand the origin of the two contrasting types of chromites.
Physics of the Earth and Planetary Interiors, Vol. 284, pp. 36-50.
Mantle
peridotite
Abstract: Interpretation of melting phase relationships of mantle peridotite and subducted basaltic crust is important for understanding chemical heterogeneity in the Earth’s interior. Although numerous studies have conducted melting experiments on peridotite and mid-ocean ridge basalt (MORB), and suggested that the solidus temperature of MORB is lower than that of peridotite at whole mantle pressure conditions, both solidus temperatures overlap within their uncertainties. In this study, we conducted simultaneous experiments on KLB-1 peridotite and normal MORB (N-MORB) at pressures from 25?GPa to 27?GPa and temperatures from 2398?K to 2673?K, to compare the solidus temperatures and their melting phase relations. The experimental results show that the solidus temperature of the N-MORB is nearly identical to the KLB-1 peridotite at 25?GPa but lower at 27?GPa. In addition, we found that the crossover of melt fractions between KLB-1 peridotite and N-MORB occurs at 25-27?GPa. These changes are likely to be attributed to the majorite-bridgmanite transition of MORB. This indicates that the dominant melting component may change depending on the location of the uppermost lower mantle. Our calculation result on the density of partial melts along the mantle geotherm suggests that partial melts of KLB-1 peridotite are gravitationally stable around the top of the transition zone, whereas partial melts of N-MORB are gravitationally stable even at the top of lower mantle. These results suggest that the distribution of partial melts may be different between KLB-1 peridotite and N-MORB in the deep Earth. Our results may be useful for understanding the fate of partial melts of peridotitic mantle and recycled basaltic crust.
Geochimica et Cosmochimica Acta, Vol. 242, pp. 165-190.
United States, Arizona
peridotite
Abstract: Scientists have known for a long time that various types of rock conduct current differently and that these differences are even more pronounced as the temperatures and pressures increase farther beneath Earth’s surface. They also know that unusual changes in electrical conductivity can signal activity down below, like migrating magma or a release of trapped fluids. Thus, electrical measurements can uncover clues about the events that trigger earthquakes and volcanic eruptions here on the surface. They can also give clues to the mantle’s structure and dynamics. However, interpreting these signals is far from straightforward. Earth scientists increasingly use electrical observations made in the field to image Earth’s crust and mantle, in particular, at subduction zones and mid-ocean ridges. An effective means of interpreting these electrical images and placing them into context with other geological observations is key to translating raw data into usable knowledge. Such knowledge includes assessing potential hazards by investigating, for example, links between fluid release and earthquake generation or the production and transport of magmatic melt from its source region to an eventual eruption. SIGMELTS is a freely available app that helps to characterize electrically conductive or resistive features detected at depth using electromagnetic observations. The objective of this Web application is to facilitate the elaboration of models of the electrical properties of crust and mantle materials, which, in turn, is used to improve the interpretation of field electromagnetic observations. A new version of SIGMELTS is now available.
Geochemical Perspectives Letters, Vol. 9, pp. 6-10. 10.7185/geochemlet.1830
Mantle
peridotites
Abstract: The origin of the peridotites that form cratonic mantle roots is a central issue in understanding the history and survival of Earth’s oldest continents. A long-standing hypothesis holds that the unusual bulk compositions of some cratonic peridotites stem from their origin as subducted oceanic serpentinite, dehydrated during subduction to form rigid buoyant keels (Schulze, 1986; Canil and Lee, 2009). We present oxygen isotope data from 93 mantle peridotites from five different Archean cratons to evaluate their possible origin as serpentinites. Cratonic mantle peridotite shows remarkably uniform ?18O values, identical to modern MORB-source mantle, that do not vary with bulk rock Si-enrichment or Ca-depletion. These data clearly conflict with any model for cratonic lithosphere that invokes serpentinite as a protolith for cratonic peridotite, and place additional constraints on cratonic mantle origins. We posit that the uniform ?18O was produced by sub-arc and/or MOR depletion processes and that the Si-enriched nature of some samples is unlikely to be related to slab melt infiltration. Instead, we suggest a peridotitic source of Si-enrichment, derived from ascending mantle melts, or a water-fluxed depleted mantle. These variably Si-enriched, cratonic mantle protoliths were then collisionally compressed into the thick cratonic roots that have protected Earth’s oldest continental crust for over 2.5 Gyr.
Earth and Planetary Science Letters, Vol. 507, pp. 175-186.
Mantle
peridotite
Abstract: To examine how the mantle lithosphere stabilises continents, we present a synthesis of the mantle beneath Zealandia in the SW Pacific Ocean. Zealandia, Earth's “8th continent”, occurs over 4.9 M km2 and comprises a fore-arc, arc and back-arc fragment rifted from the Australia-Antarctica Gondwana margin 85 Myr ago. The oldest extant crust is ?500 Ma and the majority is Permian-Jurassic. Peridotitic rocks from most known locations reveal the underpinning mantle to comprise regional domains varying from refractory (Al2O3 < 1 wt%, olivine Mg# > 92, spinel Cr# up to 80, Pt/Ir < 1) to moderately depleted (Al2O3 = 2-4 wt%, olivine Mg# ?90.5, spinel Cr# < ?60). There is no systematic distribution of these domains relative to the former arc configuration and some refractory domains underlie crust that is largely devoid of magmatic rocks. Re-depletion Os model ages have no correlation with depletion indices but do have a distribution that is very similar to global convecting mantle. Whole rock, mineral and isotopic data are interpreted to show that the Zealandia mantle lithosphere was constructed from isotopically heterogeneous convecting mantle fragments swept into the sub-arc environment, amalgamated, and variably re-melted under low-P hydrous conditions. The paucity of mafic melt volumes in most of the overlying crust that could relate to the depleted domains requires melting to have been followed by lateral accretion either during subduction or slab rollback. Recent Australia-Pacific convergence has thickened portions of the Zealandia mantle to >160 km. Zealandia shows that the generation of refractory and/or thick continental lithosphere is not restricted to the Archean. Since Archean cratons also commonly display crust-mantle age decoupling, contain spinel peridotites with extreme Cr# numbers that require low-P hydrous melting, and often have a paucity of mafic melts relative to the extreme depletion indicated by their peridotitic roots, they too may - in part - be compilations of peridotite shallowly melted and then laterally accreted at subduction margins.
Abstract: The Re-Os isotopic system is largely considered the geochronometer of choice to date partial melting of terrestrial peridotites and in constraining the evolution of Earth's dynamics from the mantle viewpoint. While whole-rock peridotite Re-Os isotopic signatures are the core of such investigations, the Re-Os dating of individual peridotite minerals—base metal sulfides (BMS) and platinum group minerals (PGM)—that are the main hosts for Re and Os in the mantle peridotites came into play two decades ago. These nanometric-micrometric BMS and PGM display an extreme complexity and heterogeneity in their 187Os/188Os and 187Re/188Os signatures that result from the origin of the BMS±PGM grains (residual vs. meta-somatic), the nature of the metasomatic agents, the transport/precipitation mechanisms, BMS±PGM mineral-ogy, and subsequent Re/Os fractionation. Corresponding whole-rock host peridotites, typically plot within the 187Os/188Os and 187Re/188Os ranges defined by the BMS±PGM, clearly demonstrating that their Re-Os signatures represent the average of the different BMS±PGM populations. The difference between the 187Os/188Os ratios of the least radiogenic BMS±PGM and the respective host peridotite increases with the fertility of the peridotite reflecting the increasing contribution of metasomatic BMS±PGM to the whole-rock mass balance of Re and Os concentrations and Os isotope compositions. Corollaries to these observations are that (1) BMS may provide a record of much older partial melting event, pushing back in time the age of the lithospheric mantle stabilization, (2) if only whole-rock peridotite Re-Os isotopic measurements are possible, then the best targets for constraining the timing of lithospheric stabilization are BMS-free/BMS-poor ultra-refractory spinel-bearing peridotites with very minimal metasomatic overprint, as their 187Os/188Os signatures may be geologically meaningful, (3) while lherzolites are “fertile” in terms of their geochemical composition, they do not have a “primitive,” unmodified composition, certainly in terms of their highly siderophile elements (HSE) and Re-Os isotopic systematics, and (4) the combined Re-Os isotopic investigations of BMS and whole-rock in BMS-rich mantle peridotites would provide a complementary view on the timing and nature of the petrological events responsible for the chemical and isotopic evolution and destruction of the lithospheric mantle. In addition, the 187Os/188Os composition of the BMS±PGM (both residual and metasomatic) within any single peridotite may define several age clusters—in contrast to the single whole-rock value—and thus provide a more accurate picture of the complex petrogenetic history of the lithospheric mantle. When coupled with a detailed BMS±PGM petrographical study and whole-rock lithophile and HSE systematics, these BMS age clusters highlight the timing and nature of the petrological events contributing to the formation and chemical and isotopic evolution of the lithospheric mantle. These BMS±PGM age clusters may match regional or the local crustal ages, suggesting that the formation and evolution of the lithospheric mantle and its overlying crust are linked, providing mirror records of their geological and chemical history. This is, however, not a rule of thumb as clear evidence of crust-mantle age decoupling also exist. Although the BMS±PGM Re-Os model ages push back in time the stabilization of lithospheric mantle, the dichotomy between Archean cratonic and circum-cratonic peridotites, and post-Archean non-cratonic peridotites and tectonites is preserved. This ability of BMS±PGM to preserve older ages than their host peridotite also underscores their survival for billions of years without being reset or reequilibrated despite the complex petrogenetic processes recorded by their host mantle peridotites. As such, they are the mantle equivalents of crustal zircons. Preservation of such old signatures in “young” oceanic peridotites ultimately rules out the use of the Re-Os signatures in both oceanic peridotites and their BMS to estimate the timescales of isotopic homogenization of the convecting mantle.
Abstract: The subduction of carbonates beyond 250-300?km, where redox conditions favour the presence of metallic iron (Fe), will result in redox reactions with the Fe dispersed in the silicate rocks. Here, we studied the effect of water on the carbonate-Fe interaction in the hydromagnesite-Fe system at 6, 8 and 16?GPa and the peridotite-CO2-H2O-Fe system at 8?GPa, using a multianvil apparatus. In all of the studied samples, we observed the formation of magnesiowüstite, graphite and carbide. Additionally, in the peridotite-CO2-H2O-Fe system, magnesiowüstite reacted with pyroxenes, resulting in olivine enrichment. Kinetic calculations performed at 8?GPa showed that, at the pressure-temperature (P-T) parameters of the ‘hot’, ‘medium’ and ‘cold’ subduction, about 40, 12 and 4?vol% of carbonates, respectively, would be reduced in the hydrous system within 1 Myr, assuming direct contact with Fe. Based on the present results, it is suggested that carbonates will largely be consumed during the characteristic subduction time to the mantle transition zone by reaction with the reduced mantle in the presence of hydrous fluid.
Abstract: A titanian clinohumite-bearing dunite was recently found in the Ulamertoq ultramafic body within the 3.0 Ga Akia Terrane of southern West Greenland. Titanian clinohumite occurs as disseminated and discrete grains. Titanian clinohumite contains relatively high amounts of fluorine, reaching up to 2.4 wt.%. The high-Fo content of olivine (Fo93) coupled with low Cr/(Cr + Al) ratio of orthopyroxene implies that the dunite host is not of residual origin after melt extraction by partial melting of the primitive mantle. Olivine grains are classified into two types based on abundances of opaque mineral inclusions: (1) dusty inclusion-rich and (2) clear inclusion-free olivines. Opaque inclusions in coarse-grained olivines are mainly magnetite. Small amounts of ilmenite are also present around titanian clinohumite grains. The observed mineral association indicates partial replacement of titanian clinohumite to ilmenite (+magnetite) and olivine following the reaction: titanian clinohumite = ilmenite + olivine + hydrous fluid. The coexistence of F-bearing titanian clinohumite, olivine, and chromian chlorite indicates equilibration at around 800-900 °C under garnet-free conditions (<2 GPa). Petrological and mineralogical characteristics of the studied titanian clinohumite-bearing dunite are comparable to deserpentinized peridotites derived from former serpentinites. This study demonstrates the importance of considering the effects of hydration/dehydration processes for the origin of ultramafic bodies found in polymetamorphic Archaean terranes.
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??m) 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??m) 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??m, 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 Geophysical Research: Solid Earth, Vol. 124, 7, pp. 6490-6503.
Mantle
peridotite
Abstract: Subducted sediments play an important role in the transport of incompatible elements back into the Earth's mantle. In recent years, studies of volcanic rocks from Samoan (Jackson et al., 2007, https://doi.org/10.1038/nature06048), NE China (Wang, Chen, et al., 2017, https://doi.org/10.1016/j.epsl.2017.02.028), and Gaussberg, Antarctica (Murphy et al., 2002, https://doi.org/10.1093/petrology/43.6.981), have shown geochemical records of a sediment?influenced mantle source from the deep Earth. However, experimental studies on the partial melting behavior of mixed sediment?peridotite mantle beyond subarc depths are very rare. In this study, we conducted experiments to investigate the partial melting behavior of mixed sediment?peridotite mantle at 4-15 GPa and 1200-1800 °C. The experimental solidi of mixed sediment?peridotite and K?feldspar?peridotite systems (Mixes A and B) cross the hot mantle geotherm at depths of around the X discontinuity (seismic discontinuity, ~300?km depth). The trace element compositions of the corresponding partial melts in Mix A showed similar characteristics to those of the Samoan basaltic lavas, potassic basalts from NE China, and Gaussberg lamproites. Therefore, the experimental results provide a possible explanation for the origin of some unusual mantle?derived volcanic rocks that contain recycled sediment signatures and have very deep origins. At depths of ~300 km (X discontinuity), a mixed sediment?peridotite source was heated by a hot?upwelling mantle and produced enriched melt. The enriched melt may interact with the surrounding mantle before incorporated into the upwelling mantle plume and becoming involved in the origin of some volcanic rocks. The experiments also provide a possible link between the enriched?mantle source in the deep mantle and the X discontinuity.
Geochimica et Cosmochimica Acta, in press available. 13p.
Africa, Cameroon
peridotite
Abstract: Highly depleted Archean peridotites have proven very amenable to Re-Os model age dating. In contrast, due to the increasing heterogeneity of mantle Os isotope compositions with time, the Re-Os system has not been as effective in dating post-Archean peridotites. The timing of depletion and accretion of post-Archean lithospheric mantle around cratons is important to understand within the context of the evolution of the continents. In an attempt to precisely date post-Archean peridotite xenoliths, we present a study of the petrology, mineralogy and geochemistry, including whole-rock Re-Os isotopes, highly siderophile elements and clinopyroxene-orthopyroxene Sr-Nd-Hf isotopes of peridotite xenoliths from Lake Nyos in the Cameroon Volcanic Line (CVL). Eight Nyos peridotite xenoliths, all fresh spinel lherzolites, are characterized by low to moderate olivine Fo contents (88.9-91.2) and low spinel Cr# (8.4-19.3), together with moderate to high whole-rock Al2O3 contents (2.0-3.7%). These chemical characteristics indicate that they are mantle residues of a few percent to <20% partial melting. However, trace element patterns of both clinopyroxene and orthopyroxene are not a pristine reflection of melt depletion but instead show various extents of evidence of metasomatic enrichment. Some of the samples contain orthopyroxene with 143Nd/144Nd lower than its coexisting clinopyroxene, which is best explained by recent short-timescale alteration, most likely by infiltration of the host basalt. Because of these metasomatic effects, the Sr-Nd isotope systematics in pyroxenes cannot sufficiently reflect melt depletion signatures. Unlike Sr-Nd isotopes, the Lu-Hf isotope system is less sensitive to recent metasomatic overprinting. Given that orthopyroxene hosts up to 33% of the Lu and 14% of the Hf in the whole rock budget of these rocks and has 176Hf/177Hf similar to, or higher than, coexisting clinopyroxene, it is necessary to reconstruct a whole-rock Lu-Hf isochron in order to constrain the melt depletion age of peridotites. The reconstructed Nyos Lu-Hf isochron from ortho- and clinopyroxenes gives an age of 2.01?±?0.18?Ga (1?), and when olivine and spinel are considered, is 1.82?±?0.14?Ga (1?). Both ages are identical within error, and they are within error of the alumina-187Os/188Os pseudo-isochron ages (1.2-2.4?Ga) produced on the peridotites from Lake Nyos, consistent with their oldest rhenium depletion Os model ages (2.0?Ga). We conclude that the Nyos peridotites, and the lithospheric mantle that they represent, were formed at ?2.0?Ga, indicating that the reconstructed whole-rock Lu-Hf isotope system can be a powerful radiometric dating tool that is complementary to and in some instances, more precise than the Re-Os isotope system in dating well-preserved post-Archean peridotites. The recognition of ?2.0?Ga subcontinental lithospheric mantle (SCLM) in the Nyos area suggests that the Nyos region was assembled as a Paleoproterozoic block, or that it represents fragments of the SCLM from the nearby Paleoproterozoic domain juxtaposed through collisional emplacement during the Pan African Orogeny. With regards to the origin of the CVL, our data reveal that the Hf isotopic compositions of the Nyos peridotites are too radiogenic to be the main source of the CVL basalts.
Abstract: Characterisation of textures in mantle peridotites has long been a subjective method, lacking precise definition or quantification. In a continuing effort to quantify textures found in mantle peridotites, we have analysed thin-sections of a wide variety of spinel and garnet peridotite xenoliths from a range of locations, using a grain-section skeleton outline method. Peridotites from ultramafic massifs have also been analysed using the same methodology. The results for all these samples lie on the same linear trend in a plot of grain-section area vs standard deviation as seen in our previous study. This confirms the utility of the quantitative method, which provides observer-independent objective numerical descriptions of textures in peridotites. In addition, two spinel peridotite xenoliths have been disaggregated using an Electric discharge disaggregation technique and were sieved to produce a grain size distribution. SEM imaging has also been used to show that the 3-D shapes of grains of the constituent minerals have concave features. Computed Tomography (CT)-scanning of separated grains and peridotite rock cores has confirmed the concave features of the constituent minerals and their consequent interlocking structures. A ‘perimeter-area’ relation technique has been used to show that the two-dimensional grain-section skeleton outlines clearly display self-similarity (i.e. fractal characteristics). Images of thin-sections were compared with known Euclidian and fractal images; both the thin-section images and the known fractal images yielded fractal dimensions, whereas the Euclidian images did not. The self-similar or fractal nature of textures of mantle peridotite rocks has also been demonstrated by using Box counting, an alternative method for fractal assessment.
Geochimica et Cosmochimica Acta, Vol. 267, pp. 179-195.
Africa, Tanzania
peridotite
Abstract: Hydrogen concentration profiles through olivine and pyroxene in peridotite xenoliths carried in rift basalts from northern Tanzania (Lashaine, Eledoi, and Kisite localities) show bell-shaped distributions, indicating that diffusive hydrogen loss has occurred in all minerals. Homogeneous major element concentrations and equilibration of hydrogen between the cores of olivine and coexisting pyroxene suggest that hydrogen loss resulted from diffusive degassing during host magma emplacement. For these samples, hydrogen diffusivities in olivine and coexisting pyroxene must be within the same order of magnitude, similar to experimentally determined diffusivities, but in contrast to previous observations made on xenolithic peridotites. We demonstrate here, for the first time using natural samples, that significant differences in activation energy is likely the primary parameter that causes the discrepancy between hydrogen diffusion in olivine and pyroxene observed in different suites of mantle xenoliths. Because hydrogen diffuses faster in olivine than in pyroxene as temperature increases, hydrogen loss in the Tanzanian mantle xenoliths must have occurred at relatively low temperatures (?750 - ?900 °C), whereas hydrogen loss observed in previous xenolith studies likely occurred at higher temperatures (?950 to > 1200 °C). Thus, the diffusive loss of hydrogen in the Tanzanian mantle xenoliths may have occurred at shallow depths or at the Earth’s surface.
Journal of Geophysical Research: Solid Earth, Vol. 124, 10, pp. 10089-10106.
Mantle
peridotite
Abstract: We present phase?equilibria experiments of a K?bearing, depleted peridotite (Mg# 92) fluxed with a mixed CO2?H2O fluid (0.5 wt.% CO2 and 0.94 wt.% H2O in the bulk) to gain insight into the stability of volatile?bearing partial melts versus volatile?bearing mineral phases in a depleted peridotite system. Experiments were performed at 850-1150 °C and 2-4 GPa using a piston?cylinder and a multianvil apparatus. Olivine, orthopyroxene, clinopyroxene, and spinel/garnet are present at all experimental conditions. Textural confirmation of partial melt is made at temperatures as low as 1000 °C at 2 GPa, 950 °C at 3 GPa, and 1000 °C at 4 GPa marking the onset of melting at 900-1000 °C at 2 GPa, 850-950 °C at 3 GPa, and 950-1000 °C at 3 GPa. Phlogopite and magnesite breakdown at 900-1000 °C at 2 GPa, 950-1000 °C at 3 GPa, and 1000-1050 °C at 4 GPa. Comparison with previously published experiments in depleted peridotite system with identical CO2?H2O content introduced via a silicic melt show that introduction of CO2?H2O as fluid lowers the temperature of phlogopite breakdown by 150-200 °C at 2-4 GPa and stabilizes partial melts at lower temperatures. Our study thus, shows that the volatile?bearing phase present in the cratonic mantle is controlled by bulk composition and is affected by the process of volatile addition during craton formation in a subduction zone. In addition, volatile introduction via melt versus aqueous fluid, leads to different proportion of anhydrous phases such as olivine and orthopyroxene. Considering the agent of metasomatism is thus critical to evaluate how the bulk composition of depleted peridotite is modified, leading to potential stability of volatile?bearing phases as the cause of anomalously low shear wave velocity in mantle domains such as mid lithospheric discontinuities beneath continents.
Americam Geophysical Union Fall meeting, 1p. Abstract
Europe, Norway
eclogites, peridotites
Abstract: The preservation of Archean cratons is typically attributed to the presence of a highly-depleted and buoyant sub-continental lithospheric mantle (SCLM) that is equally old or older than its overlying crust. Time constraints on the formation and petrological evolution of the SCLM are key to investigating its long-term evolution and role in the formation and preservation of the continental crust. Nevertheless, such constraints are difficult to obtain as well-preserved samples of the SCLM are rare and typically lack conventional chronometric minerals. The history of SCLM rocks is typically inferred on the basis of model ages, many of which indicate an Archean origin; however, these dates are difficult to link to specific mineral assemblages or chemical signatures, and the petrological and dynamic processes that these represent. Garnet Lu-Hf geochronology is one of the few chronometers that could overcome this limitation. In this study, a refined method in Lu-Hf garnet chronology was applied to fragments of the Laurentian SCLM that are now exposed as orogenic peridotites in the ultrahigh-pressure domains of the Western Gneiss Complex, Norway. The peridotite bodies comprise a variety of unusually well-preserved rock types-from dunites that record decompression and melting at >350 km depth to fertile lithologies produced by melting and fluid metasomatism. Our internal isochron results from pyrope (after exsolution from majorite) in dunite samples yielded identical Neoarchean ages; these are the first-ever obtained for mantle garnet. The ages coincide with a time interval during which there was voluminous juvenile crust formation, indicating a link between this global process and the deeply sourced mantle upwellings that these samples represent. Internal isochrons from websterite-and clinopyroxenite-hosted pyrope yielded Meso-to Neoproterozoic ages that exactly match two distinct supercontinent break-up events in the overlying continental crust. Together, the new Lu-Hf results indicate that since its extraction during a period of widespread Archean crustal growth, the Laurentian SCLM appears to have largely been at petro-physical and chemical stasis and evolved only during short pulses that ran in sync with the supercontinent cycle.
Contributions to Mineralogy and Petrology, Vol. 175, 12 pdf
Mantle
peridotites
Abstract: Experiments were performed from 950 to 1250 °C and 1.5-2.4 GPa to determine the effect of pressure (P) on the temperature (T)-dependent partitioning of Al between olivine and spinel, using mixtures of natural spinel, olivine, clino- and ortho-pyroxene. When compared to 100 kPa experiments, the results show that there is no discernible effect of pressure on the Al-in-olivine thermometer at PT conditions relevant to the spinel peridotite facies. In our experiments with high-Cr spinel, we see no change in Al in olivine from starting values, likely due to the refractory nature of high-Cr spinel. Phase boundary flourescence prevented accurate quantification of Ca in olivine in the run products by electron microprobe analysis but measurements by laser ablation are consistent with the Köhler and Brey (Geochim Cosmochim Acta 54:2375-2388, 1990) Ca-in-olivine thermobarometer. The combination of Al (for T) and Ca (for P) in olivine thus has great potential for thermobarometry in spinel facies peridotites. As a test we apply this approach to published high precision Ca and Al data for olivine from the Ray Pic spinel peridotite xenoliths from the Massif Central (De Hoog et al. Chem Geol 270:196-215, 2010). Reassuringly, the calculated PT conditions (1.0-1.8 GPa; 900-1080 °C) for all samples lie beneath the Moho, within the spinel peridotite facies and fall along a geophysically constrained geotherm.
Geochimica et Cosmochimica Acta, Vol. 270, pp. 95-111.
Russia
peridotites
Abstract: The eastern part of Asia between the North China and Siberian cratons contains orogenic belts formed by the Paleo-Asian and Pacific subduction and older continental blocks. A fundamental question regarding these and all mobile belts is the fate of the continental lithospheric mantle (CLM) during their formation, i.e. whether, or to what extent the CLM may be formed, replaced or affected during orogeny. Insights into these processes can be obtained from mantle xenoliths hosted by Cenozoic basalts in the Proterozoic Khanka block in the far eastern Russia between NE China and the Pacific coast of Asia. We report petrographic, chemical, and Os-Sr-Nd isotope data for spinel peridotite xenoliths at two Khanka sites: Sviyagin and Podgelban. The modal abundances and chemical compositions suggest that the peridotites are residues of low to moderate degrees of melt extraction from fertile mantle. They show an 187Os/188Os vs. 187Re/188Os correlation with an apparent 1.9?Ga age; the 187Os/188Os ratios are positively correlated with Al2O3 and other melt extraction indices. These results provide the first robust CLM age constraints for the eastern Central Asian Orogenic Belt (CAOB). The ages suggest that the ancient CLM of the Khanka block may be roughly coeval with reworked CLM at Hannuoba (North China craton), and that it persisted through the Phanerozoic orogenies. Moreover, despite the proximity to Phanerozoic subduction zones, the Khanka CLM shows little post-melting enrichment, e.g. the clinopyroxenes are typically LREE-depleted and have Sr-Nd isotope ratios typical of the MORB mantle. We posit that the metasomatism of the CLM, earlier proposed for North China xenolith suites and ascribed to the effects of Pacific or older subduction and related mantle upwelling, may not be widespread in the CAOB. In general, Proterozoic blocks composed of residual peridotites may be more common in the CLM of the SE Siberia and northern China, and possibly other orogenic belts, than previously thought.
Geochimica et Cosmochimica Acta, Vol. 268, pp. 405-421.
Mantle
peridotites
Abstract: Nickel is a major element in the Earth. Due to its siderophile nature, 93% of Ni is hosted in the core and the Ni isotope composition of the bulk silicate Earth might inform on the conditions of terrestrial core formation. Whether Earth’s mantle is fractionated relative to the chondritic reservoir, and by inference to the core, is a matter of debate that largely arises from the uncertain Ni isotope composition of the mantle. We address this issue through high-precision Ni isotope measurements of fertile- to melt-depleted peridotites and compare these data to chondritic meteorites. Terrestrial peridotites that are free from metasomatic overprint display a limited range in ?60/58Ni (deviation of 60Ni/58Ni relative to NIST SRM 986) and no systematic variation with degree of melt depletion. The latter is consistent with olivine and orthopyroxene buffering the Ni budget and isotope composition of the refractory peridotites. As such, the average Ni isotope composition of these peridotites (?60/58Ni = 0.115 ± 0.011‰) provides a robust estimate of the ?60/58Ni of the bulk silicate Earth. Peridotites with evidence for melt metasomatism range to heavier Ni isotope compositions where the introduction of clinopyroxene appears to drive an increase in ?60/58Ni. This requires a process where melts do not reach isotopic equilibrium with buffering olivine and orthopyroxene, but its exact nature remains obscure. Chondritic meteorites have variability in ?60/58Ni due to heterogeneity at the sampling scale. In particular, CI1 chondrites are displaced to isotopically lighter values due to sorption of Ni onto ferrihydrite during parent body alteration. Chondrites less extensively altered than the CI1 chondrites show no systematic differences in ?60/58Ni between classes and yield average ?60/58Ni = 0.212 ± 0.013‰, which is isotopically heavier than our estimate of the bulk silicate Earth. The notable isotopic difference between the bulk silicate Earth and chondrites likely results from the segregation of the terrestrial core. Our observations potentially provide a novel constraint on the conditions of terrestrial core formation but requires further experimental calibration.
Chemical Geology, DOI:101016/ j.chemgeo.2020.119464
Mantle
peridotite
Abstract: The lithospheric mantle should be depleted in base- and precious-metals as these elements are transferred to the crust during partial melting. However, some melt-depleted mantle peridotites are enriched in these ore-forming elements. This may reflect re-fertilization of the mantle lithosphere and/or sequestering of these elements by residual mantle phase(s). Both processes remain poorly understood because of the low abundances of incompatible elements in peridotite and the nugget-like distribution of digestion-resistant mantle phases that pose analytical challenges for conventional geochemical methods. Herein we report new major and trace element concentrations for a suite of mantle peridotite and pyroxenite samples from the Late Permian to Middle Triassic Nahlin ophiolite (Cache Creek terrane, British Columbia, Canada) using Laser Ablation Inductively Coupled Plasma Mass Spectrometry (LA-ICPMS) analysis of nanoparticulate powders and olivine. Compatible to moderately incompatible element concentrations suggest that Nahlin ophiolite peridotites represent residues after ?20% melt extraction. Pyroxenite dykes and replacive dunite bands are folded and closely intercalated with residual harzburgite. These field relationships, coupled with the presence of intergranular base metal sulphide, clinopyroxene and Cr-spinel at the microscale, point to percolating melts that variably re-fertilized melt-depleted mantle peridotite. Radiogenic Pb (206Pb/204Pb?=?15.402-19.050; 207Pb/204Pb?=?15.127-15.633; 208Pb/204Pb?=?34.980-38.434; n?=?45) and Os (187Os/188Os 0.1143-0.5745; n?=?58) isotope compositions for a subset of melt-depleted peridotite samples further support metasomatic re-fertilization of these elements. Other ore-forming elements are also implicated in these metasomatic reactions because some melt-depleted peridotite samples are enriched relative to the primitive mantle, opposite to their expected behaviour during partial melting. New LA-ICPMS analysis of fresh olivine further demonstrates that a significant proportion of the highly incompatible element budget for the most melt-depleted rocks is either hosted by, and/or occurs as trapped inclusions within, the olivine-rich residues. Trapped phases from past melting and/or re-fertilization events are the preferred explanation for unradiogenic Pb isotope compositions and Paleozoic to Paleoproterozoic Re-depletion model ages, which predate the Nahlin ophiolite by over one billion years.
Geochimica et Cosmochimica Acta, Vol. 278, pp. 177-198.
Africa, Cameroon
peridotites
Abstract: Highly depleted Archean peridotites have proven very amenable to Re-Os model age dating. In contrast, due to the increasing heterogeneity of mantle Os isotope compositions with time, the Re-Os system has not been as effective in dating post-Archean peridotites. The timing of depletion and accretion of post-Archean lithospheric mantle around cratons is important to understand within the context of the evolution of the continents. In an attempt to precisely date post-Archean peridotite xenoliths, we present a study of the petrology, mineralogy and geochemistry, including whole-rock Re-Os isotopes, highly siderophile elements and clinopyroxene-orthopyroxene Sr-Nd-Hf isotopes of peridotite xenoliths from Lake Nyos in the Cameroon Volcanic Line (CVL). Eight Nyos peridotite xenoliths, all fresh spinel lherzolites, are characterized by low to moderate olivine Fo contents (88.9-91.2) and low spinel Cr# (8.4-19.3), together with moderate to high whole-rock Al2O3 contents (2.0-3.7%). These chemical characteristics indicate that they are mantle residues of a few percent to <20% partial melting. However, trace element patterns of both clinopyroxene and orthopyroxene are not a pristine reflection of melt depletion but instead show various extents of evidence of metasomatic enrichment. Some of the samples contain orthopyroxene with 143Nd/144Nd lower than its coexisting clinopyroxene, which is best explained by recent short-timescale alteration, most likely by infiltration of the host basalt. Because of these metasomatic effects, the Sr-Nd isotope systematics in pyroxenes cannot sufficiently reflect melt depletion signatures. Unlike Sr-Nd isotopes, the Lu-Hf isotope system is less sensitive to recent metasomatic overprinting. Given that orthopyroxene hosts up to 33% of the Lu and 14% of the Hf in the whole rock budget of these rocks and has 176Hf/177Hf similar to, or higher than, coexisting clinopyroxene, it is necessary to reconstruct a whole-rock Lu-Hf isochron in order to constrain the melt depletion age of peridotites. The reconstructed Nyos Lu-Hf isochron from ortho- and clinopyroxenes gives an age of 2.01?±?0.18?Ga (1?), and when olivine and spinel are considered, is 1.82?±?0.14?Ga (1?). Both ages are identical within error, and they are within error of the alumina-187Os/188Os pseudo-isochron ages (1.2-2.4?Ga) produced on the peridotites from Lake Nyos, consistent with their oldest rhenium depletion Os model ages (2.0?Ga). We conclude that the Nyos peridotites, and the lithospheric mantle that they represent, were formed at ?2.0?Ga, indicating that the reconstructed whole-rock Lu-Hf isotope system can be a powerful radiometric dating tool that is complementary to and in some instances, more precise than the Re-Os isotope system in dating well-preserved post-Archean peridotites. The recognition of ?2.0?Ga subcontinental lithospheric mantle (SCLM) in the Nyos area suggests that the Nyos region was assembled as a Paleoproterozoic block, or that it represents fragments of the SCLM from the nearby Paleoproterozoic domain juxtaposed through collisional emplacement during the Pan African Orogeny. With regards to the origin of the CVL, our data reveal that the Hf isotopic compositions of the Nyos peridotites are too radiogenic to be the main source of the CVL basalts.
Abstract: The metamorphic core of the Betic-Rif orogenic chain (Alboran Domain) is made up of lower crustal rocks forming the envelope of the Ronda (Spain) and Beni Bousera (Morocco) peridotites. The deepest sections of the crustal envelopes are made of migmatitic granulites associated with diffuse acidic magmatic products, making these exposure and ideal site to investigate the textural and petrological connection between crustal anatexis and granite magmatism in the contintental crust. However, still debated is the timing of intracrustal emplacement of the peridotite bodies, with models proposing either Alpine (early Miocene) or Hercynian ages, and still uncertain is the linkage between peridotite emplacement and crustal anatexis. In this study, by combining rock textures with whole-rock geochemistry, metamorphic thermobarometry, the U-Pb zircon geochronology and the analysis of the garnet and zircon REE chemistry, we document the P-T-t evolution of the granulite facies migmatites that form the immediate envelope of the Beni Bousera peridotites of the Rif belt. A main episode of Permo-Carboniferous (ca. 300-290?Ma) deep crustal anatexis, melt extraction and migration is documented that we link to the crustal emplacement of the Beni Bousera peridotites during collapse of the Hercynian orogen. Correlation at a regional scale suggests that the Beni-Bousera section can be tentatively correlated with the pre-Alpine (Permo-Carboniferous) basement units tectonically interleaved within the orogenic structure of the Alpine chain. The results of this study provide ultimate constraints to reconstruct the tectono-metamorphic evolution of the Alboran Domain in the Western Mediterranean and impose re-assessment of the modes and rates through which Alpine orogenic construction and collapse occurred and operated in the region.
Abstract: Highly carbonated mantle xenoliths have been found in rift-related alkaline basalts at the Wadi Natash area in the southern part of the Eastern Desert of Egypt. Although all olivine and most orthopyroxene was replaced by carbonate and/or quartz, textural and mineral chemical features show that they are plagioclase-free spinel peridotites (lherzolite to harzburgite). Cr and Mg numbers (Cr#, Mg#) of Cr-spinel vary from 0.06 to 0.45 and 0.73 to 0.81, respectively. The correlation between Cr# and Mg# of the Cr-spinel in the studied xenoliths is weakly negative and its TiO2 content is slightly higher than in abyssal peridotite that was not affected by melt injection. The chemistry of ortho- and clinopyroxene suggests enstatite and chromian diopside compositions, respectively, with distinct signatures of a sub-continental mantle source. In particular, the Na2O contents (>1.0?wt%) and AlVI/AlIV ratios (1.2-2.6) of chromian diopside suggest such an origin. Two-pyroxene geothermometry indicates a temperature of about 900?°C, which is slightly lower than that of ordinary spinel peridotite xenoliths from other rift zones. It is evident that the studied peridotite xenoliths had experienced mantle processes (e.g. decompression melting, magma upwelling and metasomatism) at higher pressure than abyssal peridotites. The trace-element chemistry of clinopyroxene, e.g. high LREE/HREE ratios {(Ce/Yb)n?=?7}, high LREE contents (>3.6?ppm and up to 30.0?ppm Ce) and high Sr between >85.6?ppm and 466?ppm, indicates metasomatic alteration of the peridotite. Clinopyroxene in one sample has very low Ti/Eu and high LREE/HREE ratios. Clinopyroxene with (Ce/Yb)n higher than 3-4 and Ti/Eu ratio lower than 1500 may have experienced carbonatite or carbonate-rich melt metasomatism prior to their incorporation into the host basalt. The basalt itself is almost devoid of any carbonatization and hence the studied mantle peridotites were carbonatized before the generation of the basaltic magma but following an earlier event of K-metasomatism as indicated by the presence of phlogopite. The studied peridotites from the Wadi Natash area were altered by a carbonate-rich melt during a rifting stage. The results of the present paper indicate that the Natash basalts with their peridotite xenoliths extruded along transversal fractures of the NW-trending Nuqra-Kom Ombo-Kharit continental rift on its western shoulder in the south Eastern Desert of Egypt.
Abstract:
Water and iron are believed to be key constituents controlling the strength and density of the lithosphere and, therefore, play a crucial role in the long-term stability of cratons. On the other hand, metasomatism can modify the water and iron abundances in the mantle and possibly triggers thermo-mechanical erosion of cratonic keels. Whether local or large scale processes control water distribution in cratonic mantle remains unclear, calling for further investigation. Spinel peridotite xenoliths in alkali basalts of the Cenozoic Tok volcanic field sampled the lithospheric mantle beneath the southeastern margin of the Siberian Craton. The absence of garnet-bearing peridotite among the xenoliths, together with voluminous eruptions of basaltic magma, suggests that the craton margin, in contrast to the central part, lost its deep keel. The Tok peridotites experienced extensive and complex metasomatic reworking by evolved, Ca-Fe-rich liquids that transformed refractory harzburgite to lherzolite and wehrlite. We used polarized Fourier transform infrared spectroscopy (FTIR) to obtain water content in olivine, orthopyroxene (Opx), and clinopyroxene (Cpx) of 14 Tok xenoliths. Olivine, with a water content of 0-3 ppm H2O, was severely degassed, probably during emplacement and cooling of the host lava flow. Orthopyroxene (49-106 ppm H2O) and clinopyroxene (97-300 ppm H2O) are in equilibrium. The cores of the pyroxene grains, unlike olivine, experienced no water loss due to dehydration or addition attributable to interaction with the host magma. The water contents of Opx and Cpx are similar to those from the Kaapvaal, Tanzania, and North China cratons, but the Tok Opx has less water than previously studied Opx from the central Siberian craton (Udachnaya, 28-301 ppm; average 138 ppm). Melting models suggest that the water contents of Tok peridotites are higher than in melting residues, and argue for a post-melting (metasomatic) origin. Moreover, the water contents in Opx and Cpx of Tok peridotites are decoupled from iron enrichments or other indicators of melt metasomatism (e.g., CaO and P2O5). Such decoupling is not seen in the Udachnaya and Kaapvaal peridotites but is similar to observations on Tanzanian peridotites. Our data suggest that iron enrichments in the southeastern Siberian craton mantle preceded water enrichment. Pervasive and large-scale, iron enrichment in the lithospheric mantle may strongly increase its density and initiate a thermo-magmatic erosion. By contrast, the distribution of water in xenoliths is relatively “recent” and was controlled by local metasomatic processes that operate shortly before the volcanic eruption. Hence, water abundances in minerals of Tok mantle xenoliths appear to represent a snapshot of water in the vicinity of the xenolith source regions.
Vestnik Otdelenia nauk o Zemle RAN *** ENG, Vol. 3, doi:10.2205/2011NZ000138, 5p. Pdf * note date
Mantle
geobarometry, peridotites
Abstract: Original monomineral thermobarometers for mantle peridotites for clinopyroxene, garnet, chromite and ilmenites for the mantle peridotites were statistically calibrated on the PT estimates for mantle peridotites [Ashchepkov et al., 2010] were tested using the mineral phases obtained in high pressure experiments with the natural peridotites (380 runs) [Brey et al.,1990; 2008 etc] and eclogites (240 runs)[Dasgupta et al., 2006 etc]. In the original program of that written on FORTRAN are assembled the most reliable methods of mineral thermometers (45) and barometers (36) and oxybarometers (5), including original monomineral and methods [Ashchepkov, 2003 Ashchepkov et al., 2008; 2009; 2010; 2011] for the mantle peridotites bases on the compositions of on clinopyroxene, garnet, chromite and ilmenite. Program reads the text files, which converted from Excel. Original data include standard silicate compositions for 12 components in standard order. The text file includes 15 columns of 8 symbols. The first is file name which is the same for all the minerals in the association. The second is indicator symbol for phases. E- enstatite, D - diopside, O-olivine, S-spinel, G- garnet, I -ilmenite, A- amphibole, F - phlogopite, P-plagioclase, L- liquid, R- bulk rock. Then follow oxides: SiO2, TiO2, Al2O3, Cr2O3, FeO, MnO, MgO, CaO, Na2O, K2O, NiO, V2O3 written with 2-3 decimals. The last column may contain description of the mineral or association up to 64 symbols. Monomineral methods use calculated values for Fe#Ol or Fe#Cpx. The input from console includes file name (8 symbols) (A8), then amount of PT pairs of numbers thermometers and barometers (2I2) and one for FO2 method. Program allows input of the iteration numbers (to 25 by default). It allow to choose whether to use the calculated Fe3+ for the minerals and also. It is possible also to put fixed values of T and P (default 1000o C and 40 kbar ).
Abstract:
Decades of study have documented several orders of magnitude variation in the oxygen fugacity (fO2) of terrestrial magmas and of mantle peridotites. This variability has commonly been attributed either to differences in the redox state of multivalent elements (e.g., Fe3+/Fe2+) in mantle sources or to processes acting on melts after segregation from their sources (e.g., crystallization or degassing). We show here that the phase equilibria of plagioclase, spinel, and garnet lherzolites of constant bulk composition (including whole-rock Fe3+/Fe2+) can also lead to systematic variations in fO2 in the shallowest ~100 km of the mantle. Two different thermodynamic models were used to calculate fO2 vs. pressure and temperature for a representative, slightly depleted peridotite of constant composition (including total oxygen). Under subsolidus conditions, increasing pressure in the plagioclase-lherzolite facies from 1 bar up to the disappearance of plagioclase at the lower pressure limit of the spinel-lherzolite facies leads to an fO2 decrease (normalized to a metastable plagioclase-free peridotite of the same composition at the same pressure and temperature) of ~1.25 orders of magnitude. The spinel-lherzolite facies defines a minimum in fO2 and increasing pressure in this facies has little influence on fO2 (normalized to a metastable spinel-free peridotite of the same composition at the same pressure and temperature) up to the appearance of garnet in the stable assemblage. Increasing pressure across the garnet-lherzolite facies leads to increases in fO2 (normalized to a metastable garnet-free peridotite of the same composition at the same pressure and temperature) of ~1 order of magnitude from the low values of the spinel-lherzolite facies. These changes in normalized fO2 reflect primarily the indirect effects of reactions involving aluminous phases in the peridotite that either produce or consume pyroxene with increasing pressure: Reactions that produce pyroxene with increasing pressure (e.g., forsterite + anorthite ? Mg-Tschermak + diopside in plagioclase lherzolite) lead to dilution of Fe3+-bearing components in pyroxene and therefore to decreases in normalized fO2, whereas pyroxene-consuming reactions (e.g., in the garnet stability field) lead initially to enrichment of Fe3+-bearing components in pyroxene and to increases in normalized fO2 (although this is counteracted to some degree by progressive partitioning of Fe3+ from the pyroxene into the garnet with increasing pressure). Thus, the variations in normalized fO2 inferred from thermodynamic modeling of upper mantle peridotite of constant composition are primarily passive consequences of the same phase changes that produce the transitions from plagioclase ? spinel ? garnet lherzolite and the variations in Al content in pyroxenes within each of these facies. Because these variations are largely driven by phase changes among Al-rich phases, they are predicted to diminish with the decrease in bulk Al content that results from melt extraction from peridotite, and this is consistent with our calculations. Observed variations in FMQ-normalized fO2 of primitive mantle-derived basalts and peridotites within and across different tectonic environments probably mostly reflect variations in the chemical compositions (e.g., Fe3+/Fe2+ or bulk O2 content) of their sources (e.g., produced by subduction of oxidizing fluids, sediments, and altered oceanic crust or of reducing organic material; by equilibration with graphite- or diamond-saturated fluids; or by the effects of partial melting). However, we conclude that in nature the predicted effects of pressure- and temperature-dependent phase equilibria on the fO2 of peridotites of constant composition are likely to be superimposed on variations in fO2 that reflect differences in the whole-rock Fe3+/Fe2+ ratios of peridotites and therefore that the effects of phase equilibria should also be considered in efforts to understand observed variations in the oxygen fugacities of magmas and their mantle sources.
Abstract: The Guli and Bor-Uryakh massifs, a part of the Siberian Large igneous province (LIP) are mafic-ultramafic intrusive complexes, withstrongalkaline affinity. They contain deposits of apatite and arealsoknown to be source rocks ofOs-Ir-Ruplacers.These massifs are of great interest for petrologists worldwide, as they are composed of an unusual variety of rocks (dunites/olivinites, shonkinites, melilitites, alkali syenites and carbonatites) and being coeval with Siberian trap volcanic rocks, includingdiamondiferous kimberlites. Since mineralogical approaches based on spinel-group minerals have been proved to be efficient in constraining origin of the ultramafics, we present the first descriptive study of chromite and magnetite mineralization, observed in olivine-dominated rocks of the Guli and Bor-Uryakh intrusions. In dunites of Guli massif spinel-group minerals are dominated by Mg-poor chromite (FeMg)Cr2O4and Cr-Ti-rich magnetiteFeFe2O4, while in Bor-Uryakh massif spinel-group minerals are predominantly magnetite with only minor Mg-poor chromite.These minerals form either small euhedral inclusions in olivine or largesubhedral to anhedral grains in serpentinized fractures and interstitial space. The lattertype of grainscan have intricated irregular shapeand contain inclusions. We also observed abundant Cr-magnetite lamellae in olivine and chromite/magnetite micro-grains within olivine-hosted multiphase inclusions.Spinel (MgAl2O4) is occasionally found in intergrowths with chromite and magnetite.The obtained data show that spinel-group minerals in the massifsdo not correspond to primary-magmatic varieties and suggestextensive alteration during post-magmatic processes. Textural and chemical evidenceof substantial modification of initially-cumulative lithologies of Guli and Bor-Uryakh massifsfavorsmeta-magmatic origin for these massifs.
Abstract: Geoscientists have long been trying to answer the complicated questions of how and why Earth’s continents formed. New research suggests a solution that surprised even the investigators themselves.
Abstract: The numerous chemical and isotopic studies of oceanic basalts have shaped our perception of mantle geochemistry over the last six decades. As partial melts of Earth’s mantle, basalts are indirect tracers of mantle composition. Because the scale of isotopic heterogeneity is smaller than the scale of melt production, melts from isotopically heterogeneous mantle ingredients mix into variable blends on their way to eruption. Basalts are therefore isotopically less variable than their mantle sources. Decrypting “the message from oceanic volcanism” thus necessitates developing strategies to see through this ubiquitous sampling bias, but also acknowledging the inherent limitations imposed by investigating mantle composition through basalts. Understanding how large the bias between melts and mantle actually is requires decoding process versus source-related causes for the isotopic variability of basalts. Ultimately, deciphering the effective range of isotopic variability in Earth’s mantle is crucial for connecting isotopic signals in basalts to different materials and thus, the geologic processes that govern silicate earth evolution. Invariably, however, basalts are weighted averages of melts from isotopically different mantle constituents. As such, their incompatible element and isotopic composition is inherently biased towards the incompatible element enriched source components. The incompatible element depleted components of Earth’s mantle must therefore range to more extreme compositions than the basalts. But although isotope data from peridotites and olivine-hosted melt inclusions have extended the bounds of mantle heterogeneity, the overall extent of incompatible element depletion and mass fraction of incompatible element depleted mantle is still elusive. Mantle depletion is driven by the rate of melt extraction, or mantle processing, and thus interconnects the geochemical and geodynamical evolution of Earth’s mantle. Better constraining mantle depletion is therefore at the root of understanding our planet’s principal mode of operation.
Abstract: Unravelling the physical state and properties of mantle rocks is crucial for understanding both plate tectonics, seismic activity, and volcanism. In this context, the knowledge of accurate elastic parameters of constituent mineral phases, and their variations with pressure (P) and temperature (T), is an essential requirement, that coupled with the thermal state of the lithosphere can provide a better understanding of its petrophysics and thermochemical structure. In this paper, we present an assessment of the thermoelastic parameters [in the form of P-V-T-K Equations of State (EoS)] of orthopyroxene, clinopyroxene, spinel and garnet based on X-Ray diffraction data and direct elastic measurements available in literature. The newly developed EoS are appropriate to describe the elastic behaviour of these phases under the most relevant P-T conditions and bulk compositions of the Earth's mantle. In combination with the published EoS for mantle olivine and magnesiochromite, these EoS are suitable to calculate the physical properties of mantle peridotites and their variation with P and T. Thanks to these EoS, we can evaluate how the variations in bulk composition and thermal regimes affect the density structure of the lithospheric mantle. Accordingly, the density structure of fertile and depleted peridotitic systems was calculated along the 35, 45 and 60 mWm?2 geothermal gradients at P comprised between 1 and 8 GPa. Under very cold geothermal gradients, the density of both fertile and depleted peridotitic systems progressively increases with depth, whereas under relatively hot conditions a first downwards decrease from 1 to ca 3 GPa is observed, followed by an increase downward. In mantle sections characterized by intermediate geotherms (45 mWm?2), the behaviour of the two systems differs up to ca 4 GPa, as the density of the depleted system remains nearly constant down to this depth whereas it moderately increases in the fertile system. The results of our simplified parameterisation, in agreement with classical thermodynamic modelling, indicate that the density structure of the lithospheric mantle is predominantly controlled by the P - T gradient variations, with some compositional control mostly arising at cold-intermediate thermal conditions. Integrated by geophysical and thermodynamic modelling, the newly developed and selected EoS could provide an alternative strategy to infer the elastic properties of mineral phases and peridotite rocks, under the most relevant P-T conditions and compositions of the Earth's mantle, without requiring sets of end-member properties and solution models.
Abstract: The principal distinction between diamond substrates and the cratonic mantle roots as sampled by garnet peridotite xenoliths is the much higher proportion of harzburgite (-dunite) to lherzolite (-wehrlite) in the former (~85:15 %) compared to the latter (18:82 %). Dunitic mineralogies are common diamond substrates (~38%) but rarely documented in xenoliths (~2 %). Using mineral Mg# as an indicator of source depletion through melt extraction again documents the more depleted character of diamond substrates relative to the cratonic garnet-peridotite xenolith record. On a like-for-like paragenesis level, however, olivine inside and outside of diamond has statistically indistinguishable means in Mg#. This observation implies: (1) that the major element composition of inclusions is imposed largely by the substrate and not by the diamond forming medium and (2) that widespread Fe-rich metasomatism of the lithospheric mantle did not occur subsequent to diamond formation (Paleoarchean to Mesoproterozoic). The latter conclusion precludes neither localized metasomatic shifts in Mg#, nor metasomatism by small melt fractions/fluids subsequent to diamond formation, as such events have low fluid/rock ratios and hence limited impact on bulk rock Mg#. A distinctive feature of inclusions relative to xenolith minerals is the higher Cr/Al of garnet and chromite in diamond. Higher Cr/Al for inclusions is not limited to the harzburgitic-dunitic paragenesis, but also occurs among lherzolitic inclusions. This suggests that the almost exclusive restriction of Cr2O3 contents >13 wt% to inclusion garnets is not a consequence of higher degrees of primary melt depletion being restricted to, or preferentially preserved, in diamond substrates. Instead, the very high Cr contents in a subset of inclusions likely relate to the pressure and temperature dependence of the distribution of Cr between garnet and spinel. Experiments showed inclusion-like high Cr/Al for coexisting Cr-pyrope and Cr-spinel in harzburgite at high pressures and temperatures (>5 GPa and >1200 °C; Girnis and Brey 1999). High Cr/Al inclusion compositions thus likely reflect some diamond growth occurring over a wide range of temperatures, elevated above a cratonic geotherm during high-temperature thermal perturbations. Na and Ti are sensitive indicators of mantle metasomatism. Enrichment of Na and Ti in both inclusion and xenolith minerals is most prominent in the lherzolitic paragenesis and very intense Ti-rich metasomatism is almost entirely restricted to lherzolite xenoliths that resided at temperatures >1130 °C, i.e. above the hydrous solidus. Since equilibration temperatures of >1130 °C are common also for inclusions, the near absence of intense Ti-metasomatism in inclusions likely relates to either a diamond unfriendly character of such metasomatism or an increase in Ti-metasomatic intensity or frequency subsequent to principally Archean-Mesoproterozoic formation of peridotitic diamonds.
Abstract: Harzburgites and dunites forming the base of the Late Cretaceous-Paleocene Papuan Ultramafic Belt (PUB) and Marum ophiolites of Papua New Guinea (PNG) are amongst the most refractory mantle peridotites on Earth. We present a new integrated dataset of major element, bulk plus mineral trace element and Re-Os isotopic analyses aimed at better understanding the genesis of these peridotites. The PUB harzburgites contain olivine (Fo92-93), low-Al enstatite (less than or equal to 0.5 wt. % Al2O3 and CaO), and Cr-rich spinel (Cr# = 0.90-0.95). The Marum harzburgites are less refractory with olivine (Fo91.9-92.7), enstatite (~0.5-1.0 wt. % Al2O3 and CaO), minor clinopyroxene (diopside), and spinel (Cr# = 0.71-0.77). These major element characteristics reflect equivalent or greater levels of melt depletion than that experienced by Archean cratonic peridotites. Whereas bulk-rock heavy rare earth element (HREE) abundances mirror the refractory character indicated by the mineral chemistry and major elements, large-ion lithophile elements (LILEs) indicate a more complex melting and metasomatic history. In-situ olivine and orthopyroxene REE measurements show that harzburgites and dunites have experienced distinct melt-rock interaction processes, with dunite channels/lenses, specifically, showing higher abundances of HREE in olivine. Distinctive severe inter-element fraction of platinum group elements and Re result in complex patterns that we refer to as “M-shaped”. These fractionated highly siderophile element (HSE) patterns likely reflect the dissolution of HSE-rich phases in highly depleted peridotites by interaction with subduction-related melts/fluids, possibly high-temperature boninites. Osmium isotope compositions of the PNG peridotites are variable (187Os/188Os = 0.1204 to 0.1611), but fall within the range of peridotites derived from Phanerozoic oceanic mantle, providing no support for ancient melt depletion, despite their refractory character. This provides further evidence that highly depleted peridotites can be produced in the modern Earth, in subduction zone environments. The complex geochemistry indicates a multi-stage process for the formation of the PNG mantle peridotites in a modern geodynamic environment. The first stage involves partial melting at low-pressure (<2 GPa) and high-temperature (~1250-1350 0C) to form low-K, low-Ti tholeiitic magmas that formed the overlying cumulate peridotite-gabbro and basalt (PUB only) sequences of the ophiolites. This is inferred to have occurred in a fore-arc setting at the initiation of subduction. Later stages involved fluxing of the residual harzburgites with hydrous fluids and melts to form replacive dunites and enstatite dykes, and interaction of the residual peridotites in the overlying mantle wedge with high-temperature hydrous melts from the subducting slab to generate the extremely refractory harzburgites. This latter stage can be linked to the eruption of low-Ca boninites at Cape Vogel, and other arc-related volcanics, in a nascent oceanic island arc. Both ophiolites were emplaced shortly after when the embryonic oceanic island arc collided with the Australian continent.
Journal of Petrology, 10.1093/petrology/egac014 99p. pdf
Asia, Papua New Guinea
tectonites
Abstract: Harzburgites and dunites forming the base of the Late Cretaceous-Paleocene Papuan Ultramafic Belt (PUB) and Marum ophiolites of Papua New Guinea (PNG) are among the most refractory mantle peridotites on Earth. We present a new integrated dataset of major element, bulk plus mineral trace element and Re-Os isotopic analyses aimed at better understanding the genesis of these peridotites. The PUB harzburgites contain olivine (Fo92-93), low-Al enstatite (less than or equal to 0.5 wt. % Al2O3 and CaO), and Cr-rich spinel (Cr#?=?0.90-0.95). The Marum harzburgites are less refractory with olivine (Fo91.9-92.7), enstatite (~0.5-1.0 wt. % Al2O3 and CaO), minor clinopyroxene (diopside), and spinel (Cr#?=?0.71-0.77). These major element characteristics reflect equivalent or greater levels of melt depletion than that experienced by Archean cratonic peridotites. Whereas bulk-rock heavy rare earth element (HREE) abundances mirror the refractory character indicated by the mineral chemistry and major elements, large-ion lithophile elements indicate a more complex melting and metasomatic history. In situ olivine and orthopyroxene REE measurements show that harzburgites and dunites have experienced distinct melt-rock interaction processes, with dunite channels/lenses, specifically, showing higher abundances of HREE in olivine. Distinctive severe inter-element fraction of platinum group elements and Re result in complex patterns that we refer to as ‘M-shaped’. These fractionated highly siderophile element (HSE) patterns likely reflect the dissolution of HSE-rich phases in highly depleted peridotites by interaction with subduction-related melts/fluids, possibly high-temperature boninites. Osmium isotope compositions of the PNG peridotites are variable (187Os/188Os?=?0.1204 to 0.1611), but fall within the range of peridotites derived from Phanerozoic oceanic mantle, providing no support for ancient melt depletion, despite their refractory character. This provides further evidence that highly depleted peridotites can be produced in the modern Earth, in subduction zone environments. The complex geochemistry indicates a multi-stage process for the formation of the PNG mantle peridotites in a modern geodynamic environment. The first stage involves partial melting at low-pressure (<2 GPa) and high-temperature (~1250°C-1350°C) to form low-K, low-Ti tholeiitic magmas that formed the overlying cumulate peridotite-gabbro and basalt (PUB only) sequences of the ophiolites. This is inferred to have occurred in a fore-arc setting at the initiation of subduction. Later stages involved fluxing of the residual harzburgites with hydrous fluids and melts to form replacive dunites and enstatite dykes and interaction of the residual peridotites in the overlying mantle wedge with high-temperature hydrous melts from the subducting slab to generate the extremely refractory harzburgites. This latter stage can be linked to the eruption of low-Ca boninites at Cape Vogel, and other arc-related volcanics, in a nascent oceanic island arc. Both ophiolites were emplaced shortly after when the embryonic oceanic island arc collided with the Australian continent.
Journal of Petrology, Vol. 63, 4, 10.1093/perology/egac021
Mantle
peridotite
Abstract: The Co, Mn, Fe, and Ni contents of olivine phenocrysts and host basalts are sensitive to source mantle lithology, which suggests they may be used to constrain the processes of mantle melting and identify basalts formed from non-peridotitic (i.e. pyroxenitic) mantle sources. Here, we use a new comprehensive, forward model involving multiple parameters to simulate partitioning of Co and Mn during partial melting of the mantle in different tectonic settings: (1) polybaric continuous melting of peridotite mantle in mid-ocean ridges can generate melts that show decreasing Co and Mn with increasing degrees of melting so that the mid-ocean ridge basalts (MORBs) contain ~39-84 ?g/g Co and?~900-1600 ?g/g Mn; (2) flux-melting of the mantle wedge in subduction zones tends to produce a melt that has Co increasing from ~24 to 55 ?g/g and Mn from ~500 to 1110 ?g/g with increasing temperature; (3) melts produced by isobaric melting of the subcontinental lithospheric mantle are also sensitive to increasing temperature and have ~35-160 ?g/g Co and ~800-2600 ?g/g Mn; (4) decompression melting of peridotite related to the mantle plume generates melts containing ~45-140 ?g/g Co and?~1000-2000 ?g/g Mn, and the abundances of these metals decrease with increasing degrees of melting; and (5) partitioning behaviors of Co, Mn, and Ni during decompression melting of MORB-like pyroxenite contrast with those during decompression melting of peridotite due to the different mineralogy and compositions in mantle lithologies, and the MORB-like pyroxenite-derived melt is metal-poor with ~25-60 ?g/g Co, ~290-1600 ?g/g Mn, and?~160-340 ?g/g Ni. Although high-Ni, low-Mn forsteritic olivine phenocrysts and high melt Fe/Mn ratio have been proposed as diagnostic indicators of pyroxenitic components in the mantle, our models show that these features can be also generated by melting of peridotite at greater depth (i.e. a high pressure and temperature). To quantify the effect of high-pressure melting of peridotite on these diagnostic indicators, we modeled the correlations of melt Fe/Mn and olivine Co, Mn, and Ni contents with melting depth along the decompression melting path of a thermal plume. When Fe/Mn ratios of basalts and/or compositions of olivine phenocrysts deviate significantly from our modeled correlation lines, high-pressure melting of peridotite cannot explain these data, and the existence of pyroxenitic component in the mantle source is likely required. The pyroxenite-derived melt is modeled to be Ni-poor, but mixing with a peridotite-derived melt can strongly increase the partition coefficient of Ni between olivine and mixed melt, resulting in the generation of high-Ni olivine phenocrysts in plume-associated magmatic suites.
Contributions to Mineralogy and Petrology, Vol. 177, 44, 10.1007/s00410-022-01905-w.
Mantle
peridotites
Abstract: Devolatilization of subducting lithologies liberates COH-fluids. These may become partially sequestered in peridotites in the slab and the overlying forearc mantle, affecting the cycling of volatiles and fluid mobile elements in subduction zones. Here we assess the magnitudes, timescales and mechanism of channelized injection of COH-fluids doped with Ca2+aq, Sr2+aq and Ba2+aq into the dry forearc mantle by performing piston cylinder experiments between 1-2.5 GPa and 600-700 °C. Cylindrical cores of natural spinel-bearing harzburgites were used as starting materials. Based on mineral assemblage and composition three reaction zones are distinguishable from the rim towards the core of primary olivine and orthopyroxene grains. Zone 1 contains carbonates?+?quartz?±?kyanite and zone 2 contains carbonates?+?talc?±?chlorite. Olivine is further replaced in zone 3 by either antigorite?+?magnesite or magnesite?+?talc within or above antigorite stability, respectively. Orthopyroxene is replaced in zone 3 by talc?+?chlorite. Mineral assemblages and the compositions of secondary minerals depend on fluid composition and the replaced primary silicate. The extent of alteration depends on fluid CO2 content and fluid/rock-ratio, and is further promoted by fluid permeable reaction zones and reaction driven cracking. Our results show that COH-fluid induced metasomatism of the forearc mantle is self-perpetuating and efficient at sequestering Ca2+aq, Sr2+aq, Ba2+aq and CO2aq into newly formed carbonates. This process is fast with 90% of the available C sequestered and nearly 50% of the initial minerals altered at 650 °C, 2 GPa within 55 h. The dissolution of primary silicates under high COH-fluid/rock-ratios, as in channelized fluid flow, enriches SiO2aq in the fluid, while CO2aq is sequestered into carbonates. In an open system, the remaining CO2-depleted, Si-enriched aqueous fluid may cause Si-metasomatism in the forearc further away from the injection of the COH-fluid into peridotite.
