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101.
The ages of subcontinental lithospheric mantle beneath the North China and South China cratons are less well-constrained than the overlying crust. We report Re–Os isotope systematics of mantle xenoliths entrained in Paleozoic kimberlites and Mesozoic basalts from eastern China. Peridotite xenoliths from the Fuxian and Mengyin Paleozoic diamondiferous kimberlites in the North China Craton give Archean Re depletion ages of 2.6–3.2 Ga and melt depletion ages of 2.9–3.4 Ga. No obvious differences in Re and Os abundances, Os isotopic ratios and model ages are observed between spinel-facies and garnet-facies peridotites from both kimberlite localities. The Re–Os isotopic data, together with the PGE concentrations, demonstrate that beneath the Archean continental crust of the eastern North China Craton, Archean lithospheric mantle of spinel- to diamond-facies existed without apparent compositional stratification during the Paleozoic. The Mesozoic and Cenozoic basalt-borne peridotite and pyroxenite xenoliths, on the other hand, show geochemical features indicating metasomatic enrichment, along with a large range of the Re–Os isotopic model ages from Proterozoic to Phanerozoic. These features indicate that lithospheric transformation or refertilization through melt-peridotite interaction could be the primary mechanism for compositional changes during the Phanerozoic, rather than delamination or thermal-mechanical erosion, despite the potential of these latter processes to play an important role for the loss of garnet-facies mantle. A fresh garnet lherzolite xenolith from the Yangtze Block has a Re depletion age of ∼1.04 Ga, much younger than overlying Archean crustal rocks but the same Re depletion ages as spinel lherzolite xenoliths from adjacent Mesozoic basalts, indicating Neoproterozoic resetting of the Re–Os system in the South China Craton.  相似文献   
102.
Spatial variations in grain-size parameters (i.e. grain-size trends) contain information on sediment transport patterns. Analytical procedures have been proposed using the grain-size trend to determine net sediment transport pathways. In the first part of this study, the fundamentals of the theory are presented through methods for analysing 1D and 2D variations. The methods used are critically discussed, while pointing out some severe problems. So far, these methods suffer from limitations leading to serious interpretational errors, making it necessary to take account of two kinds of uncertainties. Inputs uncertainties are linked to the physical sediment properties as well as procedures of sampling and analysis. Model uncertainties are then discussed for each step of the grain-size trend analysis. The validity of Sediment Trend Analysis under natural conditions is tested against published field studies to determine the most appropriate variation trend to use in a specific environment. Proposals are given for each step of the procedure for optimal use of the method using a Quality Assurance (QA) approach. Further developments are proposed, such as integration into a Geographic Information System.  相似文献   
103.
The sulfur isotopic composition of carbonate associated sulfate (CAS) has been used to investigate the geochemistry of ancient seawater sulfate. However, few studies have quantified the reliability of δ34S of CAS as a seawater sulfate proxy, especially with respect to later diagenetic overprinting. Pyrite, which typically has depleted δ34S values due to authigenic fractionation associated with bacterial sulfate reduction, is a common constituent of marine sedimentary rocks. The oxidation of pyrite, whether during diagenesis or sample preparation, could thus adversely influence the sulfur isotopic composition of CAS. Here, we report the results of CAS extractions using HCl and acetic acid with samples spiked with varying amounts of pyrite. The results show a very strong linear relationship between the abundance of fine-grained pyrite added to the sample and the resultant abundance and δ34S value of CAS. This data represents the first unequivocal evidence that pyrite is oxidized during the CAS extraction process. Our mixing models indicate that in samples with much less than 1 wt.% pyrite and relatively high δ34Spyrite values, the isotopic offset imparted by oxidation of pyrite should be much less than ? 4‰. A wealth of literature exists on the oxidation of pyrite by Fe3+ and we believe this mechanism drives the oxidation of pyrite during CAS extraction, during which the oxygen used to form sulfate is taken from H2O, not O2. Consequently, extracting CAS under anaerobic conditions would only slow, but not halt, the oxidation of pyrite. Future studies of CAS should attempt to quantify pyrite abundance and isotopic composition.  相似文献   
104.
The massive sulfide deposits of the Iberian Pyrite Belt are interbedded with felsic volcanic rocks and shale, and underlain by several thousand meters of siliciclastic sedimentary rocks known as the PQ Group. Isotope geochemistry and regional geology are both consistent with equilibration of the ore-forming fluids with the PQ Group, prior to ore deposition near the former seafloor. The average Cu:Zn:Pb ratio of the PQ Group rocks (ca. 26:55:19) is similar to the weighted average of all the massive sulfide orebodies combined (ca. 25:52:23).The genetic relationship between massive sulfide deposits and a siliciclastic sedimentary metal source is explained here by a thermodynamic model, proposing that mildly reducing redox conditions imposed by equilibration with the sedimentary rocks are most critical for the formation of an effective ore-forming fluid. Relatively metal-rich but organic-poor pyrite-bearing shale undergoing dewatering of saline pore fluids is an effective source for the generation of sulfur-deficient but relatively iron and base metal-rich brines. Thus, we propose that the giant deposits of the Iberian Pyrite Belt owe their existence not to exceptionally metal-enriched (e.g., magmatic) fluids, but to the existence of a fairly ordinary but large metal source in reactive siliciclastic sediments, combined with an underlying igneous heat source and a particularly efficient mechanism of sulfide precipitation by mixing with H2S-rich fluids at or near the seafloor.Essentially similar mineral equilibria are imposed when saline fluids are buffered by typical continental basement rocks. Leaching of retrograde minerals and possibly residual salts from their magmatic or metamorphic prehistory is expected to generate similar, variably metal-rich but relatively sulfide-deficient fluids. Thus, the existence of mildly reducing rocks can be the dominant chemical control in the source of fluids generating many volcanogenic, Irish-type or sedex deposits, many of which are known to precipitate their metal load in response to biogenic sulfide addition at the ore deposition site.  相似文献   
105.
《Earth》2008,88(3-4):61-93
Sedimentological observations and palaeomagnetic data for Cryogenian glacial deposits present the climatic paradox of grounded glaciers and in situ cold climate near sea-level, glaciomarine deposition, and accompanying large (up to 40 °C) seasonal changes of temperature, all in low to near-equatorial (< 10°) palaeolatitudes (equated with geographic latitudes). Neither the “snowball Earth” nor the “slushball Earth” hypothesis can account for such strong seasonality near the palaeoequator, which together with findings from sedimentology, chemostratigraphy, biogeochemistry, micropalaeontology, geochronology and climate modelling argue against those scenarios. An alternative explanation of glaciation and strong seasonality in low palaeolatitudes is offered by a high (> 54°) obliquity of the ecliptic, which would render the equator cooler than the poles, on average, and amplify global seasonality. A high obliquity per se would not have been a primary trigger for glaciation, but would have strongly influenced the latitudinal distribution of glaciers. The principle of low-latitude glaciation on a terrestrial planet with high obliquity is validated by theoretical studies and observations of Mars. A high obliquity for the early Earth is a likely outcome of a single giant impact at 4.5 Ga, the widely favoured mechanism for lunar origin. This implies that a high obliquity could have prevailed during most of the Precambrian, controlling the low palaeolatitude of glaciations in the early and late Palaeoproterozoic and Cryogenian. It is postulated that the obliquity changed to < 54° between the termination of the last Cryogenian low-palaeolatitude glaciation at ≤ 635 Ma and the initiation of Late Ordovician–Early Silurian circum-polar glaciation at 445 Ma.The High Obliquity, Low-latitude Ice, STrong seasonality (HOLIST) hypothesis for pre-Ediacaran glaciation emerges favourably from numerous glacial and non-glacial tests. The hypothesis is in accord with such established or implied features of Cryogenian glaciogenic successions as extensive and long-lived open seas, an active hydrological cycle, aridity and palaeowesterly (reversed zonal) winds in low palaeolatitudes, and the apparent diachronism or non-correlation of some low-palaeolatitude glaciations. A pre-Ediacaran high obliquity also offers a viable solution of the faint young Sun paradox of a warm Archaean Earth. Furthermore, reduction of obliquity during the Ediacaran–early Palaeozoic would have yielded a more habitable globe with much reduced seasonal stresses and may have been an important factor influencing the unique evolutionary events of the Ediacaran and Cambrian. The palaeolatitudinal distribution of evaporites cannot discriminate unambiguously between high- and low-obliquity states for the pre-Ediacaran Earth. Intervals of true polar wander such as postulated by others for the Ediacaran and Early Cambrian imply major mass-redistributions within the Earth at those times, which may provide a potential mechanism for reducing the obliquity during the Ediacaran–early Palaeozoic.  相似文献   
106.
《Earth》2008,86(3-4):85-116
Wetland plant communities persisted though much of the Pennsylvanian in Euramerica and are the dominant coal forming vegetation in this region. Distribution of these floras show a dramatic decline at the end of the Carboniferous with many of the plant genera and species becoming extinct by the onset of the Permian. This has been correlated with climate change and in particular aridification associated with northwards plate motion and Euramerica moving into the doldrums, but is also associated with the Variscan orogeny and forefront destroying large areas of formerly lowland basinal settings. Other factors may include Pennsylvanian glaciations as evidenced by cyclothem and rhythmical deposition in lowlying wetland settings, and change in eustatic base level. Evidence from Euramerica demonstrates extinction of this kind of wetland biota by the earliest Permian and the development of drier floras including conifer dominated assemblages. However, new data from other parts of the world, most notably North China, confirm this model and highlight the presence of similar coal swamps ranging from the Late Pennsylvanian through the Permian. In this paper we summarise and synthesize recent taxonomic and systematic investigations undertaken on the plant fossils from the Pennsylvanian Benxi Formation – the oldest recognised wetland plant community in China – and the Early Permian Taiyuan Formation – the best preserved wetland plant community from China. Results indicate a remarkable similarity of the Pennsylvanian–Early Permian floras of North China with the older assemblages in the Pennsylvanian of Euramerica, and the presence of typical ‘Euramerican’ coal swamp plant families, genera and in some cases species in China. Conclusions include the presence of the Ameriosinian phytogeographical realm uniting Euramerica and northern Cathaysia at this time, coal swamps in the Permian of North China evolving from a ‘Euramerican’ origin, and the dramatic floral turnover at the end of the Carboniferous representing a regional event rather than a global extinction episode. Patterns of plant distribution through this interval have profound implications on established palaeogeographical models and support continental connection between Euramerica and Cathaysia before the end of the Carboniferous, contradicting ideas of Cathaysian island biogeography and biotic distinction. Continental connection appears to be related to glacial eustatic low-stand and previously shallow marine environments becoming vegetated. Also important is the fact that in both Euramerica and North China the pattern of floristic demise within wetland plant communities are similar to each other, implying the same causal mechanisms, with plants occupying waterlogged positions being the most severely devastated. However, ecosystem demise occurred at the end of the Carboniferous in Euramerica and in the middle Permian in North China, but in both cases the primary cause was climate change.  相似文献   
107.
Thirty-four silicate and oxide inclusions large enough for in situ WDS electron microprobe analysis were exposed by grinding/polishing of 19 diamonds from the Kelsey Lake Mine in the Colorado-Wyoming State Line Kimberlite district. Eighteen olivines, seven Cr-pyropes, four Mg-chromites, and one orthopyroxene in 15 stones belong to the peridotite (P) suite and three garnets and one omphacite in three stones belong to the eclogite (E) suite. The fact that this suite is dominated by the peridotite population is in stark contrast to the other diamond suites studied in the State Line district (Sloan, George Creek), which are overwhelmingly eclogitic. Kelsey Lake olivine inclusions are magnesian (17 of 18 grains in 9 stones are in the range Fo 92.7-93.1), typical of harzburgitic P-suite stones worldwide, but unlike the more Fe-rich (lherzolitic) Sloan olivine suite. Mg-chromites (wt% MgO = 12.8-13.8; wt% Cr2O3 = 61.4-66.6) are in the lower MgO range of diamond inclusion chromites worldwide. Seven harzburgitic Cr-pyropes in five stones have moderately low calcium contents (wt% CaO = 3.3-4.3) but are very Cr-rich (wt% Cr2O3 = 9.7-16.7). A few stones have been analyzed by SIMS for carbon isotope composition and nitrogen abundance. One peridotitic stone is apparently homogeneous in carbon isotope composition (δ13CPDB = −6.2‰) but with variable nitrogen abundance (1296-2550 ppm). Carbon isotopes in eclogitic stones range from “normal” for the upper mantle (δ13CPDB = −5.5‰) to somewhat low (δ13CPDB = −10.2‰), with little internal variation in individual stones (maximum difference is 3.6‰). Nitrogen contents (2-779 ppm) are lower than in the peridotitic stone, and are lower in cores than in rims. As, worldwide, harzburgite-suite diamonds have been shown to have formed in Archean time, we suggest that the Kelsey Lake diamond population was derived from a block of Archean lithosphere that, at the time of kimberlite eruption, existed beneath the Proterozoic Yavapai province. The mixed diamond inclusion populations from the State Line kimberlites appear to support models in which volumes of Wyoming Craton Archean mantle survive buried beneath Proterozoic continental crust. Such material may be mixed with eclogitic/lherzolitic regimes emplaced beneath or intermingled with the Archean rocks by Proterozoic subduction.  相似文献   
108.
A systematic investigation on silica contents and silicon isotope compositions of bamboos was undertaken. Seven bamboo plants and related soils were collected from seven locations in China. The roots, stem, branch and leaves for each plant were sampled and their silica contents and silicon isotope compositions were determined. The silica contents and silicon isotope compositions of bulk and water-soluble fraction of soils were also measured. The silica contents of studied bamboo organs vary from 0.30% to 9.95%. Within bamboo plant the silica contents show an increasing trend from stem, through branch, to leaves. In bamboo roots the silica is exclusively in the endodermis cells, but in stem, branch and leaves, the silica is accumulated mainly in epidermal cells. The silicon isotope compositions of bamboos exhibit significant variation, from −2.3‰ to 1.8‰, and large and systematic silicon isotope fractionation was observed within each bamboo. The δ30Si values decrease from roots to stem, but then increase from stem, through branch, to leaves. The ranges of δ30Si values within each bamboo vary from 1.0‰ to 3.3‰. Considering the total range of silicon isotope composition in terrestrial samples is only 7‰, the observed silicon isotope variation in single bamboo is significant and remarkable. This kind of silicon isotope variation might be caused by isotope fractionation in a Rayleigh process when SiO2 precipitated in stem, branches and leaves gradually from plant fluid. In this process the Si isotope fractionation factor between dissolved Si and precipitated Si in bamboo (αpre-sol) is estimated to be 0.9981. However, other factors should be considered to explain the decrease of δ30Si value from roots to stem, including larger ratio of dissolved H4SiO4 to precipitated SiO2 in roots than in stem. There is a positive correlation between the δ30Si values of water-soluble fractions in soils and those of bulk bamboos, indicating that the dissolved silicon in pore water and phytoliths in soil is the direct sources of silicon taken up by bamboo roots. A biochemical silicon isotope fractionation exists in process of silicon uptake by bamboo roots. Its silicon isotope fractionation factor (αbam-wa) is estimated to be 0.9988. Considering the distribution patterns of SiO2 contents and δ30Si values among different bamboo organs, evapotranspiration may be the driving force for an upward flow of a silicon-bearing fluid and silica precipitation. Passive silicon uptake and transportation may be important for bamboo, although the role of active uptake of silicic acid by roots may not be neglected. The samples with relatively high δ30Si values all grew in soils showing high content of organic materials. In contrast, the samples with relatively low δ30Si values all grew in soil showing low content of organic materials. The silicon isotope composition of bamboo may reflect the local soil type and growth conditions. Our study suggests that bamboos may play an important role in global silicon cycle.  相似文献   
109.
δ34S and sulfate concentrations were determined in snow pit samples using a thermal ionization mass spectrometric technique capable of 0.2‰ accuracy and requires ≈5 μg (0.16 μmol) natural S. The technique utilizes a 33S-36S double spike for instrumental mass fractionation correction, and has been applied to snow pit samples collected from the Inilchek Glacier, Kyrgyzstan and from Summit, Greenland. These δ34S determinations provide the first high-resolution seasonal data for these sites, and are used to estimate seasonal sulfate sources. Deuterium (δD) and oxygen (δ18O) isotope data show that the Inilchek and Summit snow pit samples represent precipitation over ≈20 months.The δ34S values for the Inilchek ranged from +2.6 ± 0.4‰ to +7.6 ± 0.4‰ on sample sizes ranging from 0.3 to 1.8 μmol S. δ34S values for Greenland ranged from +3.6 ± 0.7‰ to +13.3 ± 5‰ for sample sizes ranging from 0.05 to 0.29 μmol S. The concentration ranged from 92.6 ± 0.4 to 1049 ± 4 ng/g for the Inilchek and 18 ± 9 to 93 ± 6 ng/g for the Greenland snow pit. Anthropogenic sulfate dominates throughout the sampled time interval for both sites based on mass balance considerations. Additionally, both sites exhibit a seasonal signature in both δ34S and concentration. The thermal ionization mass spectrometric technique has three advantages compared to gas source isotopic methods: (1) sample size requirements of this technique are 10-fold less permitting access to the higher resolution S isotope record of low concentration snow and ice, (2) the double spike technique permits δ34S and S concentration to be determined simultaneously, and (3) the double spike is an internal standard.  相似文献   
110.
Earth’s core may contain C, and it has been suggested that C in the core could stabilize the formation of a solid inner core composed of Fe3C. We experimentally examined the Fe-C system at a pressure of 5 GPa and determined the Fe-C phase diagram at this pressure. In addition, we measured solid metal/liquid metal partition coefficients for 17 trace elements and examined the partitioning behavior between Fe3C and liquid metal for 14 trace elements. Solid metal/liquid metal partition coefficients are similar to those found in one atmosphere studies, indicating that the effect of pressure to 5 GPa is negligible. All measured Fe3C/liquid metal partition coefficients investigated are less than one, such that all trace elements prefer the C-rich liquid to Fe3C. Fe3C/liquid metal partition coefficients tend to decrease with decreasing atomic radii within a given period. Of particular interest, our 5 GPa Fe-C phase diagram does not show any evidence that the Fe-Fe3C eutectic composition shifts to lower C contents with increasing pressure, which is central to the previous reasoning that the inner core may be composed of Fe3C.  相似文献   
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