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Chemical geology
Elsevier
Chemical geology

Elsevier

0009-2541

Chemical geology/Journal Chemical geologySCIISTPAHCIEI
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    Nd-Hf isotopic systematics of the arc mantle and their implication for continental crust growth

    Hao, HongdaCampbell, Ian H.Park, Jung-Woo
    13页
    查看更多>>摘要:The 143Nd/144Nd and 176Hf/177Hf values of depleted mid-ocean ridge basalt (MORB) mantle have long been used to calculate the Nd and Hf model ages and constrain the growth rate of the continental crust. However, because continental crust forms principally at subduction zones, the appropriate 143Nd/144Nd and 176Hf/177Hf for use in model age calculations are those of the mantle wedge that underlies the juvenile magmatic arcs. In this study, we compile the Nd and Hf isotopic compositions of the modern island arc volcanic rocks. The average 143Nd/144Nd value obtained for the arc mantle is 0.512959 (eNd = +6.3), with upper and lower 95% confidence uncertainties of 0.513115 (eNd = +9.3) and 0.512613 (eNd = -0.5), respectively. The average obtained for 176Hf/177Hf is 0.283144 (eHf = +13.2) with upper and lower limits of 0.283272 (eHf = +17.7) and 0.282927 (eHf = +5.5), respectively, at the 95% confidence level. The Nd and Hf isotopic compositions of the modern island arc volcanic rocks can be divided into three populations, the high, transitional and low e arc mantle populations, that reflect a combination of mantle heterogeneity and additions of different slab-derived components to the mantle wedge. The high e arc mantle (HAM) population (eNd +5.7 and eHf +10) were metasomatized by the transfer of unradiogenic Nd and Hf from pelagic sediments, and Fe-Mn crusts and nodules, to the mantle wedge, the HAM by fluid dominate process and the TAM by a combination of sediment melts and fluids. In contrast, melts derived from subducted sediments, particularly zircon-rich turbidites, play a more important role in the low e arc mantle population (LAM, eNd < +5.7 and eHf < +10). The average of both Nd and Hf isotopic data for the arc mantle, together with the 95% confidence limits, are used to define the arc mantle growth curves and their uncertainties. We suggest that these arc mantle growth curves should be used to calculate Nd and Hf model ages and constrain the growth rate of the continental crust.

    Oxidized mantle sources of HIMU- and EM-type Ocean Island Basalts

    Nicklas, Robert W.Hahn, Rachel K. M.Willhite, Lori N.Jackson, Matthew G....
    11页
    查看更多>>摘要:Oxygen fugacity (fO2) is a fundamental variable in igneous petrology with utility as a potential tracer of recycled high Fe+3/EFe surficial materials in the sources of mantle-derived lavas. It has been postulated that ocean island basalts (OIB) have elevated fO2 relative to mid-ocean ridge basalts (MORB) owing to higher average Fe+3/EFe in their source regions. To examine this issue, trace-element systematics of olivine grains are reported from OIB lavas with HIMU (high-??; Mangaia, Canary Islands), enriched mantle (EM; Samoa; Sa??o Miguel in the Azores Islands) and depleted MORB mantle (DMM; Pico in the Azores Islands) Sr-Nd-Pb-Os isotope signatures, in order to constrain the fO2 of each magmatic system. Despite sampling distinct mantle reservoirs based on radiogenic isotope systematics, these OIB suites show similar fO2, ranging from +0.8 to +2.6 AFMQ, with an average of +1.5 ?? 0.8 AFMQ, largely higher than MORB using the same oxybarometry method at +0.6 ?? 0.2 AFMQ. The studied OIB show no correlation between fO2 and bulk rock isotopic ratios or calculated parental magma compositions. The lack of correlations with isotopic signatures likely results from radiogenic isotope signatures being hosted in volumetrically minor trace element enriched mantle lithologies, while Fe+3/EFe ratios that act as the primary control on fO2 are controlled by the volumetrically dominant mantle component. Higher fO2 in many OIB relative to MORB implies that they sample a uniformly high Fe+3/EFe plume source mantle that may be the result of either a common oxidized oceanic crust-rich reservoir parental to many modern plume lavas, or preservation of un-degassed and oxidized mantle domains formed shortly after core formation.

    The Mo- and U-isotope signatures in alternating shales and carbonate beds of rhythmites: A comparison and implications for redox conditions across the Cambrian-Ordovician boundary

    Li, JieAzmy, KaremKendall, Brian
    14页
    查看更多>>摘要:The Green Point Formation (GPF) of the Cow Head Group in western Newfoundland (Canada) includes the Global Boundary Stratotype Section and Point (GSSP) for the Cambrian-Ordovician (epsilon-O) boundary on Laurentia. This formation is composed primarily of thick, deep subtidal to slope deposits (rhythmites) of alternating lime mudstones and shale interbeds. Here, we employ isotopic and elemental data of Mo and U of these shales and carbonates to better understand their depositional environments and the open ocean redox conditions at the epsilon-O transition. The variability of delta Mo-98(auth) (-0.40 to +3.16 parts per thousand) indicates variable aqueous sulfide concentrations ([H2S](aq)) in bottom waters or porewaters during deposition of the shales. A significant positive correlation of shale [Mo](auth) with [U](auth) coupled with low Mo concentrations compared to Phanerozoic euxinic shales further points to weakly reducing (similar to dysoxic/suboxic to anoxic) benthic conditions with H2Saq primarily confined to porewaters. For the lime mudstones, the delta Mo-98 variability (-0.30 to +2.34 parts per thousand) suggests variable [H2S](aq) in porewaters during early diagenesis. Low Mo concentrations ([Mo](carb) = 0.25 +/- 0.80 mu g/g, 2 sigma) and a poor correlation of [Mo](carb) with delta Mo-98(carb) indicate weak sulfidic ([H2S](aq )< 11 mu M) porewater conditions and possibly dysoxic to suboxic bottom environments. Thus, the delta Mo-98(carb) may not track the delta Mo-98 of basin waters because of low [H2S](aq) in porewaters and insignificant accumulation of authigenic Mo during early diagenesis. This explanation is consistent with a poor correlation between delta Mo-98(carb) and the delta U-238 of basin waters (estimated from delta U-238(carb)). A cautious examination of Mo-EF/U-EF, delta Mo-98(auth), and delta U-238(auth) of the shales suggests that the GPF was likely deposited in a basin with topographic barriers. During deposition of the lower and middle part of the studied interval, the barriers in combination with sea-level fluctuations may have caused partial isolation of the local basin from the open ocean. Rapid sea-level rises in the earliest Ordovician greatly increased the connectivity between the local basin and the open ocean, resulting in remarkable increases in Mo-EF/U-EF, [Mo](auth), and [U](auth) of the shales. The delta U-238 of the earliest Ordovician open oceans, inferred from delta U-238(carb), exhibited perturbations and an average value of -0.78 +/- 0.33 parts per thousand (2 sigma), reflecting oceanic redox oscillations and expanded ocean euxinia compared to the modern oceans.

    Dissolution of the smithsonite-rhodochrosite (ZnCO3-MnCO3) solid solutions in aqueous solution at 25 degrees C

    Zhu, YinianYu, XiaolingPan, ShufenNong, Peijie...
    15页
    查看更多>>摘要:A series of smithsonite-rhodochrosite solid solutions [(Zn1-xMnx)CO3] (X-Mn = 0.00-1.00) were prepared in lab to study their dissolution process in aqueous solution. The molar ratios Mn/(Zn + Mn) of the synthetic solids (X-Mn) were very close to that of the starting mixtures. The X-ray diffraction (XRD) patterns of the synthetic solids showed continuously peak shifting to lower 2 theta value with the increasing of X-Mn. For the dissolution in the nitrogen-degassed and the air-saturated water, the Zn and Mn contents in aqueous phase went up quickly to a constant value; after dissolution, the weak (200) peak of Zn-5(CO3)(2)(OH)(6) (hydrozincite) emerged in the XRD patterns of the solids with X-Mn = 0.00-0.30. For the dissolution in the carbon-dioxide-saturated water, the Zn and Mn contents in water reached high values quickly after 48 h similar to 120 h, and then declined to a stable value. After 270 d of dissolution, the aqueous molar ratios Mn/(Zn + Mn) were greater than or close to X-Mn of the corresponding solids. For the dissolution in the nitrogen-degassed, the air-saturated and the carbon-dioxide-saturated waters at 25 degrees C, the mean log IAP values (ion activity product) at the equilibrium state (approximate to solubility product log K-sp) were determined to be -10.56, -10.54 and - 10.71 for smithsonite, and - 10.29, -10.26 and - 10.18 for rhodochrosite, respectively. With the increasing of X-Mn the log IAP values increased non-linearly from -10.54 similar to -10.71 to -10.18 similar to -10.29, while the Delta Gf degrees decreased linearly from -735.08 to -736.04 kJ/mol and - 813.99 to -814.63 kJ/mol. The constructed Lippmann diagrams showed that the (Zn1-xMnx)CO3 solid solutions dissolved incongruently, and the dissolution data points moved progressively up and exceeded the solutus curve, and then move along the (Zn1-xMnx)CO3 saturation curves from left to right or right to left for the solids with lower X-Mn (0.10-0.30) and higher X-Mn (0.40-0.90), respectively.

    Carbon and oxygen isotope analysis of CO2 trapped in silicate minerals

    van der Lubbe, Jeroen H. L.Verdegaal-Warmerdam, Suzanne J. A.Postma, OnnoNikogosian, Igor K....
    13页
    查看更多>>摘要:Knowledge of the carbon and oxygen isotope composition of CO2-rich inclusions in crust- or mantle-derived minerals is crucial for a more quantitative understanding of cycling of volatiles between Earth's deep and surficial reservoirs. In this study, we present a crushing method for analysis of combined carbon and oxygen stable isotope compositions of small (<= nmole) amounts of CO2 in fluid and melt inclusions. During crushing, the released CO2 was cryo-trapped, and subsequently introduced into a Gas Bench II coupled to a Delta(plus )Isotope Ratio Mass Spectrometry (IRMS). Reference standard CO2 introduced in the crusher chamber was analysed to a precision better than similar to 0.3 and similar to 0.4 parts per thousand (1 sigma) for carbon and oxygen, respectively. Analysis of previously analysed samples validates that the crushing technique can be applied to CO2-rich fluid inclusions in quartz samples as small as 0.2 to 5 mg. CO2-rich quartz samples were analysed from the UHT-Bakhuis Granulite Belt (Suriname) and Val Nalps (Switzerland) as well as forsterite-rich olivine-hosted melt inclusions from Vulsini volcanic district (Italy). The carbon isotope compositions obtained from the quartz samples allow discrimination between different sources within the crust and mantle. In contrast, the oxygen isotopic signatures of the fluid inclusions containing water appear affected by isotopic exchange between CO2 and H2O in the inclusions, where for the free-water fluid inclusions can reflect the pristine delta O-18 value. Crushing of olivine grains with CO2 melt-inclusions displayed instantaneous adsorption of the released CO2, which leads to low CO2 yields, and considerable oxygen and carbon isotope fractionation, hampering reliable isotopic determinations. We conclude that the delta C-13 and delta O-18 values from CO2-rich inclusions can be used as an indicator of the CO2 source and to evaluate mantle CO2 outgassing and release from storages within Earth's crust. The method presented can be readily applied to determine carbon and oxygen isotopic compositions of CO2 (4.5(-10) mol) in small amounts of fluid-inclusion bearing quartz.

    Carbonatite metasomatism, the key to unlocking the carbonatite-phoscorite-ultramafic rock paradox

    Vasyukova, O. V.Williams-Jones, A. E.
    10页
    查看更多>>摘要:One of the features of carbonatite-phoscorite complexes that has received comparatively little attention is that many of them are surrounded by large bodies of ultramafic rocks. Although it is generally assumed that all the rocks are of igneous origin, there is disagreement over whether the carbonatites and phoscorites are genetically related to the ultramafic rocks. This is despite the fact that in complexes where they have been dated, these three suites of rocks are identical in age. A major challenge for any igneous hypothesis is the paradox posed by the observation that the ultramafic and carbonatitic magmas are the products of very high and very low degrees of partial melting of the mantle, respectively. We resolve this paradox by proposing a hypothesis, in which the ultramafic rocks are metasomatic in origin. According to this hypothesis, a carbonatitic magma, generated by partial melting of carbonated mantle, acts as the agent of metasomatism. The interaction of this magma with quartz-rich rocks, including granites and gneisses, transforms them into ultramafic rocks. This is made possible by the extremely low viscosity of the magma that allows it to pervasively infiltrate the wall rocks. As a result, Mg, Ca and other components are transferred to the host, leading to the crystallisation of minerals such as olivine, clinopyroxene and biotite, and the loss of CO2 from the system. Because of its low viscosity, the carbonatitic magma is emplaced as numerous intrusions, ranging in width from the micron to the metre scale, that progressively transform the host rocks into ultramafic rocks. As this metasomatism proceeds, the Na concentration of the magma gradually increases and eventually becomes high enough to permit large scale assimilation of Si (and Al) and the generation of an alkaline silicate magma that is emplaced at the margins of complexes, forming ijolites. The metasomatism and assimilation are envisaged as a front that moves progressively from the conduit to the limits of the complex, producing an outward zonation from dunite through clinopyroxenite to ijolite or from clinopyroxenite to ijolite directly. Whether the zonation is fully developed or dominated by a single zone, e.g., dunite or clinopyroxenite, depends on the initial composition of the carbonatitic magma and/or the degree of progress of the metasomatic reaction. The processes described above constitute the "silicate stage" of carbonatite-phoscorite-ultramafic rock complex development and are marked by the complete consumption of the carbonatitic magma. During the waning stages of the formation of these complexes, metasomatism by new batches of carbonatitic magma is restricted to remnants of reactive wall rocks adjacent to the magma conduit. Consequently, the magma is only partially consumed. This results in a residual liquid that is enriched in phosphate and iron and crystallises phoscorite. We refer to this as the "phoscorite stage" of carbonatite-phoscorite-ultramafic rock complex development. The final, "carbonatite stage", is marked by the cessation of metasomatic activity and the crystallisation of carbonatites from batches of magma that are unaffected by interaction with the wall rocks and are compositionally identical to those that initiated the "silicate stage". This model explains the spatial association of the different rock types, in which the complexes are zoned outwards from a core of carbonatite, through a zone enriched in phoscorite, into a broad halo of ultramafic/ultrabasic rocks. In so doing, the model accounts for the many features of these complexes that have not been adequately explained in previous genetic models.

    Effects of contact metamorphism on the lithium content and isotopic composition of kerogen in coal

    Teichert, ZebadiahEble, Cortland F.Bose, MaitrayeeWilliams, Lynda B....
    13页
    查看更多>>摘要:Lithium isotopes (delta Li-7) in coals have been shown to increase with thermal maturity, suggesting preferential release of Li-6 from kerogen to porefluids. This has important implications for paleoclimate studies based on delta Li-7 of buried marine carbonates, which may incorporate Li from porefluids during recrystallization. Here, the Li content and isotopic composition of macerals from two coal seams intruded by dikes, were studied as a function of temperature across a thermal gradient into the unmetamorphosed coal. Samples were collected in Colorado (USA) from a Vermejo Fm. coal seam intruded by a mafic-lamprophyre dike and compared to a Dutch Creek No.2 coal seam intruded by felsic-porphyry dike; a potential source of Li-rich fluids. The Li-content and Li-isotope compositions of coal macerals were measured in situ by Secondary Ion Mass Spectrometry (SIMS). The macerals of the Vermejo coal samples, buried to VRo 0.68% (T-max = 104 degrees C), contained <1.5 mu g/g Li with an average vitrinite delta Li-7 of -28.4 +/- 1.6 parts per thousand, while liptinite and inertinite were heavier, averaging -15.4 +/- 3.6 parts per thousand and - 10.5 +/- 3.7 parts per thousand, respectively. The contact metamorphosed vitrinite/coke showed the greatest change with temperature with delta Li-7 18 to 37 parts per thousand heavier than the unmetamorphosed vitrinite. The Dutch Creek coal, buried to VRo 1.15% (T-max = 147 degrees C), prior to dike emplacement, may have released Li during burial, as less isotopic change was observed between contact metamorphosed and unmetamorphosed macerals. Overall, Li contents were < 1 mu g/g, and the vitrinite in metamorphosed coal had delta Li-7 values 8 to 21 parts per thousand heavier than the unmetamorphosed coal. SIMS measurements on macerals near the dike did not show an increase in Li-content indicative of Li derived from dike fluids, however previous bulk measurements that included silicates showed slightly higher (2-3 mu g/g) Li-contents near the dike, suggesting possible Li incorporation from dike fluid into metamorphic silicates. A negative correlation was observed between Li-content and C-12(+)/Si-3(0)+ count ratios, indicating that at metamorphic temperatures Li becomes concentrated in silicates.

    Origin of paratacamite in the Kuqa Basin, Xinjiang, China: Defined by Cu isotope values

    Cao, Yangtong
    10页
    查看更多>>摘要:Isotopes of Cu in some copper minerals have been used to trace the origin of metallogenic materials. However, little is known about paratacamite, a sedimentary-type Cu mineral whose formation is closely related to brines and evaporites. The Kuqa Basin is filled with a huge thickness of evaporite deposits and is located in the northern margin of the Tarim Basin, Xinjiang, northwestern China. Here, we report a study of paratacamite from the Kuqa Basin and infer its genesis from the mineral assemblage and Cu isotopes of paratacamite. Paratacamite is widely distributed in basin deposits coexisting with saline minerals in fractures and joint planes in fault/fracture zones. Cu isotopic compositions (delta Cu-65) of paratacamite range from -0.49 parts per thousand. to 1.02 parts per thousand, with a mean of 0.41 parts per thousand. These values suggest that Cu in the paratacamite originated from Cu-bearing brine that was derived from the leaching of metallic ions from surrounding rocks and migrated along and upward through faults, fractures, and joint planes and ascended to the surface while cooling. On the basis of the paragenetic association of paratacamite with saline minerals in the studied samples, the occurrence of paratacamite is inferred to have been controlled by a crystallisation sequence of saline minerals with accompanying evaporation and concentration of brines from which gypsum, secondary glauberite, paratacamite, and halite were crystallised in turn. Differences in Cu isotopic compositions among the samples from the four studied mineralisation occurrences of Kezier, Yanshuigou, Daxiagu, and Dishui may be due to variation in the processes of Cu enrichment involving brines, such as Cu extraction from different rock layers, the migration and evaporation of Cu-bearing brine, and mineral deposition.

    Preface - XIth Silicate Melt Workshop

    Dingwell, D. B.Hess, K-URichet, P.Wilke, M....
    1页

    Response of nitrogen isotopes to paleo-environment and organic carbon accumulation in a Late Paleozoic alkaline lake, Junggar Basin

    Xia, LiuwenCao, JianJin, JunXiang, Baoli...
    12页
    查看更多>>摘要:The geochemistry of nitrogen (N) in ancient lacustrine systems, especially in alkaline conditions, is poorly understood. To fill the knowledge gap, we investigated alkaline lacustrine sediments of the Upper Paleozoic Fengcheng Formation (ca. 300 Ma) in the Mahu Sag, Junggar Basin, northwestern China. Based on the general characteristics and stratigraphic variations in N isotopes, their relationship to the paleo-environmental setting and type/accumulation of organic matter were evaluated. The lacustrine sediments can be divided into alkaline (815N 10???12???) and circum-neutral (815N < 10???12???) groups in general. The geochemical N cycle was mainly controlled by the pH of the lake water, and ammonia volatilization triggered N isotopic fractionation. In contrast, N isotopes are not significantly affected by the salinity and redox state of the water mass. The 815N, particularly for the alkaline group, exhibit a correlation with the type of organism present (i.e., the algae/bacteria ratio), and also the hydrocarbon-generation potential and type of organic matter. This reflects the response of lake water pH to the types of organisms present and accumulation of organic matter. The N isotopic compositions of lacustrine sediments, and the factors that control this, are more complex than in the marine system, and are dependent on the biomass and paleo-environmental setting.