Variable influence of the atmospheric flux on the trace metal chemistry of oceanic suspended matter

The particulate concentrations of 17 trace metals, Al, Sc, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, Se, Ag, Sb, Au, Hg, Pb and Th have been measured in the marine atmosphere (58 samples) and in the deep waters (35 samples) of the Tropical North Atlantic. For oceanic suspended matter, our results are similar to those in samples from the Atlantic and the Pacific Oceans collected during the GEOSECS Program. Based on these results, we have made a flux balance for the mixed layer between input via the atmosphere and removal through small and large particles. These data show that the primary flux of suspended aluminosilicates in the Tropical North Atlantic is attributable to the atmospheric input. Elements Sc, Th, Fe, V, Mn, Co and Cr show high correlation with Al in the marine atmosphere. Of these elements, Fe, Mn, V, Co and Cr are influenced by additional processes such as biological, in the marine environment. For elements Ni, Cu, Zn, Se, Ag, Sb, Au, Hg and Pb, we observe high enrichments (relative to average crustal material) in the marine atmosphere which may be due, at least partially, to the influence of anthropogenic sources. These metals also show similar enrichments in deep ocean suspended matter. Model calculations indicate that the atmospheric flux may not control the deep ocean particulate chemistry of Ni, Cu, Zn, Ag, Sb, Au and Hg. Hence it is likely that, for these elements, the enrichment in the ocean is due to processes within the marine regime, for example their involvement in the biological cycle of the ocean. For Se and Pb, the atmospheric source looks to be the dominant contribution to their particulate concentration in seawater. In the deep North Atlantic, particulate Pb appears to be mostly of anthropogenic origin, which is not the case for Se.     

Trace elements in ocean ridge basalts

A correlary of sea floor spreading is that the production rate of ocean ridge basalts exceeds that of all other volcanic rocks on the earth combined. Basalts of the ocean ridges bring with them a continuous record in space and time of the chemical characteristics of the underlying mantle. The chemical record is once removed, due to chemical fractionation during partial melting. Chemical fractionations can be evaluated by assuming that peridotite melting has proceeded to an olivine-orthopyroxene stage, in which case the ratios of a number of magmaphile elements in the extracted melt closely match the ratios in the mantle. Comparison of ocean ridge basalts and chondritic meteorites reveals systematic patterns of element fractionation, and what is probably a double depletion in some elements. The first depletion is in volatile elements and is due to high accretion temperatures of a large percentage of the earth from the solar nebula. The second depletion is in the largest, most highly charged lithophile elements (“incompatible elements”), probably because the mantle source of the basalts was melted previously, and the melt, enriched in these elements, was removed. Migration of melt relative to solid under ocean ridges and oceanic plates, element fractionation at subduction zones, and fractional melting of amphibolite in the Precambrian are possible mechanisms for depleting the mantle in incompatible elements. Ratios of transition metals in the mantle source of ocean ridge basalts are close to chondritic, and contrast to the extreme depletion of refractory siderophile elements, the reason for which remains uncertain. Variation of ocean ridge basalt chemistry along the length of the ridge has been correlated with ridge elevation. Thus chemically anomalous ridge segments up to 1000 km long appear to broadly coincide with regions of high magma production (plumes, hot spots). Basalt heterogeneity at a single location indicates mantle heterogeneity on a smaller scale. Variation of ocean ridge basalt chemistry with time has not been established, in fact, criteria for recognizing old oceanic crust in ophiolite terrains are currently under debate. The similarity of rare earth element patterns in basalt from ocean ridges, back-arc basins, some young island arcs, and some continental flood basalts illustrates the dangers of tectonic labeling by rare earth element pattern.     

Heat flow from the earth’s interior depending on inner parameters variations

The approximate equality of heat flows on the land and the ocean; high heat flow values on the middle oceanic ridges; a relationship of heat flow with age of tectogenesis; the extremely low heat flow values are considered as main evidence for any theoretical explanation. The deviation of surface heat flow from its equilibrium value is considered. Computing analysis of high temperature heat transfer coefficients is given. Some aspects of numerical techniques of the thermal history of the Earth are discussed. The influence of sudden and gradual formation of the Earth Crust on the surface heat flow is considered.     

Ultradeep diamonds originate from deep subducted sedimentary carbonates

Diamonds are renowned as the record of Earth’s evolution history. Natural diamonds on the Earth can be distinguished in light of genetic types as kimberlitic diamonds (including peridotitic diamonds and eclogitic diamonds), ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds. According to the inclusion mineralogy, most diamonds originated from continental lithospheric mantle at depths of 140–250 km. Several localities, however, yield ultradeep diamonds with inclusion compositions that require a sublithospheric origin (>~250 km). Ultradeep diamonds exhibit distinctions in terms of carbon isotope composition, N-concentration, mineral inclusions and so on. The present study provides a systematic compilation concerning the features of ultradeep diamonds, based on which to expound their genesis affinity with mantle-carbonate melts. The diamond-parental carbonate melts are proposed to be stemmed from the Earth’s crust through subduction of oceanic lithosphere. Ultradeep diamonds are classified into a subgroup attaching to kimberlitic diamonds grounded by formation mechanism, and present connections in respect of carbon origin to eclogitic diamonds, ultrahigh-pressure metamorphic diamonds and ophiolitic diamonds.     

The age of ferroan anorthosite 60025: oldest crust on a young Moon?

SmNd isotopic data for mineral separates from the ferroan anorthosite 60025 define a precise isochron of 4.44 ± 0.02Ga age. This age is roughly 110 m.y. younger than the formation of the first large solid objects in the solar nebula, as recorded by the radiometric ages of the differentiated meteorites. In the magma ocean model for early lunar differentiation, ferroan anorthosites are the first crustal rocks to form on the Moon. If the Moon is as old as the oldest meteorites, the relatively young age determined for 60025 implies either that the magma ocean did not form synchronously with lunar formation, or that the magma ocean required over 100 m.y. before reaching the stage of ferroan anorthosite crystallization. Alternatively, we propose that the accumulated body of radiogenic isotope data for lunar rocks permit the Moon to be as young as 4.44–4.51 Ga. If so, isotopic evidence for chemical differentiation on the Earth at about this same time suggests that the formation of the Moon is reflected in the chemical evolution of the Earth. This, in turn, is consistent with the idea that the materials that now make up the Moon were derived from the Earth, perhaps ejected by collision between the Earth and another very large planetesimal during the final stages of accumulation of the terrestrial planets. Terrestrial origin models for the Moon lessen the requirement that the Earth and Moon each have near chondritic relative abundances of the refractory elements and could require that certain chemical and isotopic characteristics of both bodies be considered in the framework of the chemical mass-balance of the combined Earth-Moon system.     

Calcium isotope fractionation in coccoliths of cultured Calcidiscus leptoporus, Helicosphaera carteri, Syracosphaera pulchra and Umbilicosphaera foliosa

Four species of marine calcifying algae, the coccolithophores Calcidiscus leptoporus, Helicosphaera carteri, Syracosphaera pulchra and Umbilicosphaera foliosa were grown in laboratory cultures under temperatures varying between 14 and 23 °C, and one species, C. leptoporus, under varying [CO₃²⁻], ranging from 105 to 219 μmol/kg. Calcium isotope compositions of the coccoliths resemble in both absolute fractionation and temperature sensitivity previous calibrations of marine calcifying species e.g. Emiliania huxleyi (coccolithophores) and Orbulina universa (planktonic foraminifera) as well as inorganically precipitated CaCO₃, but also reveal small species specific differences. In contrast to inorganically precipitated calcite, but similar to E. huxleyi and O. universa, the carbonate ion concentration of the medium has no statistically significant influence on the Ca isotope fractionation of C. leptoporus coccoliths; however, combined data of E. huxleyi and C. leptoporus indicate that the observed trends might be related to changes of the calcite saturation state of the medium. Since coccoliths constitute a significant portion of the global oceanic CaCO₃ export production, the Ca isotope fractionation in these biogenic structures is important for defining the isotopic composition of the Ca sink of the ocean, one of the key parameters for modelling changes to the marine Ca budget over time. For the present ocean our results are in general agreement with the previously postulated and applied mean value of the oceanic Ca sink (Δ_sed) of about − 1.3‰, but the observed inter- and intra-species differences point to possible changes in Δ_sed through earth history, due to changing physico-chemical conditions of the ocean and shifts in floral and faunal assemblages.     

Oceanic Loading and Local Distortions at the Baksan,Russia, and Gran Sasso,Italy, Strain Stations

Reliable use of strain data in geophysical studies requires their preliminary correction for ocean loading and various local distortions. These effects, in turn, can be estimated from the tidal records which are contributed by solid and oceanic loading. In this work, we estimate the oceanic tidal loading at two European strain stations (Baksan, Russia, and Gran Sasso, Italy) by analyzing the results obtained with the different Earth and ocean models. The influence of local distortions on the strain measurements at the two stations is estimated.     

Siderophile and chalcophile element abundances in oceanic basalts, Pb isotope evolution and growth of the Earth''s core

We have investigated the hypothesis that mantle Pb isotope ratios reflect continued extraction of Pb into the Earth's core over geologic time. The Pb, Sr and Nd isotopic compositions, and the abundance of siderophile and chalcophile elements (W, Mo and Pb) and incompatible lithophile elements have been determined for a suite of ocean island and mid-ocean ridge basalt samples. Over the observed range in Pb isotopic compositions for oceanic rocks, we found no systematic variation of siderophile or chalcophile element abundances relative to abundances of similarly incompatible, but lithophile, elements. The high sensitivity of theMo/Pr ratio to segregation of Fe-metal or S-rich metallic liquid (sulfide) and the observed constantMo/Pr ratio rules out the core formation model as an explanation for the Pb paradox. The mantle and crust have the sameMo/Pr and the sameW/Ba ratios, suggesting that these ratios reflect the ratio in the Earth's primitive mantle.

Our data also indicate that thePb/Ce ratio of the mantle is essentially constant, but the presentPb/Ce ratio in the mantle ( 0.036) is too low to represent the primitive value ( 0.1) derived from Pb isotope systematics. HigherPb/Ce ratios in the crust balance the lowPb/Ce of the mantle, and crust and mantle appear to sum to a reasonable terrestrialPb/Ce ratio. The constancy of thePb/Ce ratio in a wide variety of oceanic magma types from diverse mantle reservoirs indicates this ratio is not fractionated by magmatic processes. This suggests crust formation must have involved non-magmatic as well as magmatic processes. Hydrothermal activity at mid-ocean ridges may result in significant non-magmatic transport of Pb from mantle to crust and of U from crust to mantle, producing a higherU/Pb ratio in the mantle than in the total crust. We suggest that the lower crust is highly depleted in U and has unradiogenic Pb isotope ratios which balance the radiogenic Pb of upper crust and upper mantle. The differences between thePb/Ce ratio in sediments, this ratio in primitive mantle, and the observed ratio in oceanic basalts preclude both sediment recycling and mixing of primitive and depleted reservoirs from being important sources of chemical heterogeneities in the mantle.     

Regionalized models for the thermal evolution of the Earth

Traditional models for the heat loss in oceanic and continental regions are combined into a regionalized model for the thermal evolution of the Earth. The need for regionalization is obvious when one considers that the mantle loses 3 to 4 times as much heat per unit area in oceanic regions than in continental areas. The present-day rate of heat loss together with a geochemical estimate of the concentration of heat-producing elements in the Earth fixes the response time of the thermally convecting mantle. The response time in turn can be used to select the most reasonable representation for mantle convection in terms of the sensitivity of viscosity on temperature and layering versus mantle-wide circulation. Present geochemical estimates of the bulk composition of the Earth are most easily reconciled with the observed heat flow if the mantle is layered and its rheology is slightly less temperature dependent than generally assumed. The layered system can produce sufficiently high temperatures to explain the high-magnesian komatiites of the Archean. One difficulty with the models is that they predict widespread melting at shallow depth in the early stages of Earth history but do not address how such melting affects and alters the heat transfer mechanisms.     

Gabbroic xenoliths from La Palma, Tenerife and Lanzarote, Canary Islands: evidence for reactions between mafic alkaline Canary Islands melts and old oceanic crust

Gabbroic and hornblendite xenoliths from La Palma, Tenerife and Lanzarote fall into three main groups based on petrography and chemistry. One group (comprising all xenoliths from Lanzarote and some from La Palma) consists of highly deformed orthopyroxene-bearing gabbroic rocks that show a strong affinity to N-MORB and oceanic gabbro cumulates in terms of mineral chemistry and REE relations. However, they show mild enrichment in the most incompatible elements (particularly Rb+Ba±K) relative to intermediate and heavy REE, and their Sr–Nd isotope ratios fall within or close to the N-MORB field. The second group (60% of the xenoliths from La Palma) are gabbroic cumulates with zoned clinopyroxenes (Ti–Al-poor cores, Ti–Al-rich rims) and reaction rims of hornblende, biotite and clinopyroxene on other phases. Their trace-element and Sr–Nd isotope relations are in general transitional between N-MORB cumulates and Canary Islands alkali basalts, but they show strong enrichment in Rb, Ba and K relative to other strongly incompatible elements. The third group (comprising some xenoliths from La Palma and all those from Tenerife) are undeformed gabbroic and hornblendite rocks in which hornblende and biotite appear to belong to the primary assemblage. These rocks show strong affinities to Canary Islands alkali basaltic magmas with respect to mineral, trace-element, and Sr–Nd isotope chemistry. The first two groups are interpreted as fragments of old oceanic crust which have been mildly to strongly metasomatized through reactions with Canary Islands alkaline magmas. The reaction process is a combination of enrichment in elements compatible with biotite (and hornblende), and simple mixing between N-MORB cumulates and trapped alkaline magmas. The third group represents intrusions/cumulates formed from mafic alkaline Canary Islands magmas. Modeling indicates that locally up to 50% new material has been added to the old oceanic crust through reactions with ocean island basalts. Reactions and formation of cumulates do not represent simple underplating at the mantle/crust boundary, but have taken place within the pre-existing oceanic crust, and are likely to have significantly thickened the old oceanic crust.     

Geochemistry of late Cenozoic lavas on Kunashir Island, Kurile Arc

Middle Miocene to Quaternary lavas on Kunashir Island in the southern zone of the Kurile Arc were examined for major, trace, and Sr–Nd–Pb isotope compositions. The lavas range from basalt through to rhyolite and the mafic lavas show typical oceanic island arc signatures without significant crustal or sub-continental lithosphere contamination. The lavas exhibit across-arc variation, with increasingly greater fluid-immobile incompatible element contents from the volcanic front to the rear-arc; this pattern, however, does not apply to some other incompatible elements such as B, Sb, and halogens. All Sr–Nd–Pb isotope compositions reflect a depleted source with Indian Ocean mantle domain characteristics. The Nd and Pb isotope ratios are radiogenic in the volcanic front, whereas Sr isotope ratios are less radiogenic. These Nd isotope ratios covary with incompatible element ratios such as Th/Nd and Nb/Zr, indicating involvement of a slab-derived sediment component by addition of melt or supercritical fluid capable of mobilizing these high field-strength elements and rare earth elements from the slab. Fluid mobile elements, such as Ba, are also elevated in all basalt suites, suggesting involvement of slab fluid derived from altered oceanic crust. The Kurile Arc lavas are thus affected both by slab sediment and altered basaltic crust components. This magma plumbing system has been continuously active from the Middle Miocene to the present.     

Isotopic inferences on the chemical structure of the mantle

Variations in the isotopic composition of rocks derived from the upper mantle can be used to infer the chemical history and structure of the Earth's interior. The most prominent material in the upper mantle is the source of mid-ocean ridge basalts (MORB). The MORB source is characterized by a general depletion in incompatible elements caused by the extraction of the continental crust from the mantle. At least three other isotopically distinct components are recognized in the suboceanic mantle. All three could be generated by the recycling of near surface materials (oceanic crust, pelagic sediments, continental lithospheric mantle) into the mantle by subduction. Therefore, the isotope data do not require a compositionally layered mantle, but neither do they deny the existence of such layering. Correlations between the volumetric output of plume volcanism with the reversal frequency of the Earth's magnetic field, and between the geographic distribution of isotopic variability in oceanic volcanism with seismic tomography suggest input of deep mantle material to surface volcanism in the form of deep mantle plumes. Volcanism on the continents shows a much wider range in isotopic composition than does oceanic volcanism. The extreme isotopic compositions observed for some continental magmas and mantle xenoliths indicate long-term (up to 3.3 Gyr) preservation of compositionally distinct material in thick (>200 km) sections of continental lithospheric mantle.     

A theoretical prediction of chemical zonation in early oceans(>520 Ma)

Early oceans(520 Ma) were characterized by widespread water-column anoxia, stratification, and limited oxidant availability, which are comparable to the chemical characteristics of modern marine sedimentary pore-waters in productive continental margins. Based on this similarity and our current understanding of the formation mechanism of early Earth ocean chemistry, we propose an idealized chemical zonation model for early oceans that includes the following redox zones(from shallow nearshore to deep offshore regions): oxic, nitrogenous(NO3?-NO2?-enriched), manganous-ferruginous(Mn2+ or Fe2+-enriched), sulfidic(H2S-enriched), methanic(CH4-enriched), and ferruginous(Fe2+-enriched). These zones were dynamically maintained by a combination of processes including surface-water oxygenation by atmospheric free oxygen, nitrate reduction beneath the chemocline, nearshore manganese-iron reduction, sulfate reduction, methanogenesis, and hydrothermal Fe2+ inputs from the deep ocean. Our modified "euxinic wedge" model expands on previous versions of this model, providing a more complete theoretical framework for the chemical zonation of early Earth oceans that helps to explain observations of unusual Mo-S-C isotope patterns. This model may provide a useful foundation for future studies of ocean chemistry evolution and elemental biogeochemical cycles in early Earth history.     

Mo marine geochemistry and reconstruction of ancient ocean redox states

Molybdenum(Mo) proxies, including bulk concentration and isotopic composition, have been increasingly used to reconstruct ancient ocean redox states. This study systematically reviews Mo cycles and their accompanying isotopic fractionations in modern ocean as well as their application in paleo-ocean redox reconstruction. Our review indicates that Mo enrichment in sediments mainly records the adsorption of Fe-Mn oxides/hydroxides and chemical bonding of H2 S. Thus, Mo enrichment in anoxic sediments generally reflects the presence of H2 S in the water column or pore waters. In addition to the effect of euxinia, sedimentary Mo enrichment is related to the size of the oceanic Mo reservoir. Given these primary mechanisms for oceanic Mo cycling, Mo abundance data and Mo/TOC ratios acquired from euxinic sediments in geological times show that fluctuations of the oceanic Mo reservoir are well correlated with oxygenation of the atmosphere and oceans and suggest that oxygenation occurred in phases. Mo proxies suggest that Mo isotopes in strongly euxinic sediments reflect the contemporaneous Mo isotopic composition of seawater, but other processes such as iron-manganese(Fe-Mn) adsorption and weak euxinia can result in different fractionations. Diagenesis may complicate Mo enrichment and its isotopic fractionation in sediments. With appropriate constraints on the Mo isotopic composition of seawater and various outputs, a Mo isotope mass-balance model can quantitatively reconstruct global redox conditions over geological history. In summary, Mo proxies can be effectively used to reconstruct oceanic redox conditions on various timescales due to their sensitivity to both local and global marine redox conditions. However, given the complexity of geochemical processes, particularly the effects of diagenesis, further work is required to apply Mo proxies to ancient oceans.     

Post-collisional magmatism in Wuyu basin,central Tibet: evidence for recycling of subducted Tethyan oceanic crust

The trachyte and basaltic trachyte and intruded granite-porphyry of Gazacun formation of Wuyu Group in central Tibet are Neogene shoshonitic rocks. They are rich in LREE, with a weak to significant Eu negative anomalies. The enriched Rb, Th, U, K, negative HFS elements Nb, Ta, Ti and P, and Sr, Nd and Pb isotope geochemistry suggest that the volcanic rocks of Wuyu Group originated from the partial melting of lower crust of the Gangdese belt, with the involvement of the Tethyan oceanic crust. It implies that the north-subducted Tethys ocean crust have arrived to the lower crust of Gangdese belt and recycled in the Neogene magmatism.     

Roles of different physical processes in upper ocean responses to Typhoon Rammasun (2008)-induced wind forcing

This study investigates the roles of different physical processes in the oceanic response to tropical cyclones(TCs) in the Pacific, using an ocean general circulation model with several numerical experiments. A case study is focused on Typhoon Rammasun, which passed through the northwestern tropical Pacific in May 2008. TC-induced wind stress fields are extracted using a locally-weighted regression(Loess) method from a six-hourly Cross-Calibrated Multi-Platform satellite scatterometer wind product. By comparing model experiments with TC wind forcing being explicitly included or not, the effects of TC on the ocean are isolated in a clean way. The local oceanic response is characterized by a cooling in the surface layer that persists along the typhoon track as a cold wake, and a deepening of the mixed layer(ML). The TC-induced wind can affect the ocean through the momentum effects, the ML processes(the stirring effect on the ML depth), and heat flux(via wind speed), repectively.Analyses of numerical experiments with these different underlying processes explicitly represented or not indicate that vertical mixing and upwelling are dominant processes responsible for surface cooling, while the surface heat flux also plays a nonnegligible role. Specifically, vertical mixing, upwelling and surface heat flux account for respectively ～53%, ～31% and ～16% of the sea surface temperature cooling. However, for the ML response, the vertical mixing and surface heat flux are dominant processes for the ML deepening, while the contribution from upwelling process is negligible. This study provides new insights into how TC-indcued wind forcing affects the ocean by isolating each different individual process in a clear way, which differs from previous direct heat budget analyses.     

Seasonal variability of tides in the deep northern South China Sea

Tides are the major energy source for ocean mixing, regulating the variation of oceanic circulation and sediment transport in the deep sea. Here twenty months of high-resolution current profiles, which were observed via a mooring system at a water depth of 2100 m in the northern South China Sea(SCS), are used to investigate seasonal variability in deep-sea tides.Spectral analysis shows that tides in this region are dominated by diurnal tide, and both diurnal and semidiurnal tide are vertical mode-1 dominant. Baroclinic diurnal tidal current exhibits pronounced seasonal variability, showing its kinetic energy was the strongest in summer, and the maximum depth-averaged value was up to 86.7 cm~2 s~(-2), which was about 1.5 times of that in winter and twice that in spring and autumn. In contrast, baroclinic semidiurnal tide displays no evident seasonal variability. Such seasonal variability in baroclinic tide was mainly modulated by the barotropic forcing from the Luzon Strait. On the other hand,two anticyclonic eddies and one cyclonic eddy, which originated off southwestern Taiwan in winter, crossed the mooring system.The cyclonic eddy had weak impact on current velocity in the deep sea, but the two deep-reaching anticyclonic eddies enhanced the current velocity through the full-water column by inducing strong subinertial flows. Consequently, the kinetic energy of tides was strengthened and the incoherent variance of baroclinic diurnal tide increased in winter, which contributed ～85% of the variability in diurnal tide. Meanwhile, the velocity of baroclinic diurnal tide was reduced in winter, which was attributed to the weakened stratification induced by the passage of anticyclonic eddies in the deep sea. The seasonal variability of tides in the deep northern SCS can provide a dynamic mechanism for interpreting sediment transport processes in the deep sea on different time scales.     

Core formation and chemical equilibrium in the Earth—II: Chemical consequences for the mantle and core

We present here a new model of core formation which is based on the current understanding of planetary accretion and discuss its implications for the chemistry of the Earth's mantle and core. Formation of the Earth by hierarchical accretion of progressively larger bodies on a time scale much longer than that of solid body differentiation in the nebula indicates that a significant fraction of metal in the core could be inherited from preterrestrially differentiated planetesimals. An analysis of the segregation of this iron to form the core suggests that most of the metal settles to the core without interaction with silicates; only a small fraction of the metal chemically equilibrates at high temperatures and pressures with the silicates. The siderophile element abundances in the mantle are considered to be a consequence of a two-step equilibration with iron, once preterrestrially in the planetesimals at low temperatures and pressures, and later in the Earth at high temperatures and pressures. The highly siderophile elements such as Re, Au and the platinum group elements in the mantle are essentially excluded from silicates from the preterrestrial equilibration. We attribute the abundances of these elements in the mantle to the later equilibration in the Earth at substantially reduced metal-silicate partition coefficients (D^met/sil), for which there is a considerable experimental evidence now. Mass balance considerations constrain the fraction of core metal involved in such an equilibration at approximately 0.3 – 0.5%. The model accounts for the levels and the near-chondritic ratios of the highly siderophile elements in the mantle. The mantle abundances of the less siderophile elements are largely determined by preterrestrial metal-silicate equilibrium and are not significantly affected by the second equilibration. The extreme depletion of sulfur and the lack of silicate melt-sulfide signature in the noble metal abundances in the mantle are natural consequences of this mode of core formation. Sulfur was added to the magma ocean during the high-T, high-P equilibration in the Earth, not extracted from it by sulfide segregation to the core. Except for Ni and Co, the overall siderophile abundances of the mantle can be well matched in this two-step equilibration model.

The mantle characteristics of Ni and Co are unique to the Earth and hence suggest a terrestrial process as the likely cause. One such process is the flotation and addition of olivine to the primitive upper mantle. In our model of core formation, neither the elemental and isotopic data of Re---Os, nor the low sulfur content of the mantle remains as an objection to the existence of a magma ocean and olivine flotation.

The small fraction of core metal that equilibrates with silicates at high T and P suggests that the light elements O, Si or H are unimportant in the core, leaving S (and possibly C) as prime candidates. Sulfur, as FeS associated with incoming iron metal, is directly sequestered to the core along with the bulk of the iron metal. It appears unlikely that other light elements can be added to the core after its formation. U and Th are excluded from the core but the model allows for entry of some K; however, the extent to which K serves as a heat source in the core remains uncertain.

The model is testable in two ways. One is by investigation of the metal-silicate partitioning at high temperatures and pressures under magma ocean conditions to determine if the (D^met/sil) values are lowered to the levels required in the model. The other is by experiments to determine if a solvus closure between metal and silicate liquids occurs at high temperatures relevant to a magma ocean.     

Reconstructions of the <Superscript>14</Superscript>С cosmogenic isotope content from natural archives after the last glacial termination

Data on the content of the ¹⁴C cosmogenic isotope in tree rings, which were obtained as a result of laboratory measurements, are often used when solar activity (SA) is reconstructed for previous epochs, in which direct observations are absent. However, these data contain information not only about SA variations but also about changes in the Earth climatic parameters, such as the global temperature and the CO₂ content in the Earth’s atmosphere. The effect of these variations on the ¹⁴C isotope content in different natural reservoirs after the last glacial termination to the middle of the Holocene is considered. The global temperature and the CO₂ content increased on this time interval. In this case the ¹⁴C absolute content in the atmosphere increased on this time interval, even though the ¹⁴С to ¹²С isotope concentration ratio (as described by the Δ¹⁴С parameter) decreased. These variations in the radiocarbon absolute content can be caused by its redistribution between natural reservoirs. It has been indicated that such a redistribution is possible only when the rate of carbon exchange between the ocean and atmosphere depends on temperature. The values of the corresponding temperature coefficient for the 17–10 ka BC time interval, which make it possible to describe the carbon redistribution between the ocean and atmosphere, have been obtained.     

Post-collisional magmatism in Wuyu basin,central Tibet: evidence for recycling of subducted Tethyan oceanic crust

The trachyte and basaltic trachyte and intruded granite-porphyry of Gazacun formation of Wuyu Group in central Tibet are Neogene shoshonitic rocks. They are rich in LREE, with a weak to significant Eu negative anomalies. The enriched Rb, Th, U, K, negative HFS elements Nb, Ta, Ti and P, and Sr, Nd and Pb isotope geochemistry suggest that the volcanic rocks of Wuyu Group originated from the partial melting of lower crust of the Gangdese belt, with the involvement of the Tethyan oceanic crust. It implies that the north-subducted Tethys ocean crust have arrived to the lower crust of Gangdese belt and recycled in the Neogene magmatism.