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1.
New data for the direct measurement of the isotopic composition of neodymium in Atlantic Ocean seawater are compared with previous measurements of Pacific Ocean seawater and ferromanganese sediments from major ocean basins. Data for Atlantic seawater are in excellent agreement with Nd isotopic measurements made on Atlantic ferromanganese sediments and are distinctly different from the observed compositions of Pacific samples. These results clearly demonstrate the existence of distinctive differences in the isotopic composition of Nd in the waters of the major ocean basins and are characteristic of the ocean basin sampled. The average εNd(0) values for the major oceans as determined by data from seawater and ferromanganese sediments are as follows: Atlantic Ocean,εNd(0) ? ?12 ± 2; Indian Ocean,εNd(0) ? ?8 ± 2; Pacific Ocean,εNd(0) ? ?3 ± 2. These values are considerably less than εNd(0) value sources with oceanic mantle affinities indicating that the REE in the oceans are dominated by continental sources. The difference in the absolute abundance of143Nd between the Pacific and Atlantic Oceans corresponds to ～106 atoms143Nd per gram of seawater. The correspondence between the143Nd/144Nd in seawater and in the associated sediments suggests the possible application of this approach to paleo-oceanography.Distinctive differences in εNd(0) values are observed in the Atlantic Ocean between deep-ocean water associated with North Atlantic Deep Water and near-surface water. This suggests that North Atlantic Deep Water may be relatively well mixed with respect to Nd isotopic composition whereas near-surface water may be quite heterogeneous, reflecting different sources for surface waters relative to deep water. This suggests that it may be possible to distinguish the sources of water masses within an ocean basin on the basis of Nd isotopic composition.The Nd isotopic variations in seawater are used to relate the residence time of Nd and mixing rates between the oceans.  相似文献   

2.
A variety of Fe, Mn and trace-metal-enriched Mesozoic pelagic sediments are associated with the tectonically emplaced Antalya Complex in southwestern Turkey. Palaeotectonic settings represented within the complex comprise a continental platform, passing laterally through a Mesozoic passive margin into a zone of marginal oceanic crust, formed during the early stages of continental separation. The origins of the metalliferous sediments are elucidated using mineralogical, major, trace element and REE data, and comparisons with oceanic and ophiolite-related sediments.Late Triassic deposition during the initial continental separation was mostly terrigenous, including detrital carbonate derived from adjacent reef complexes. During the Jurassic and Early Cretaceous the passive margin underwent accumulation of fine-grained terrigenous matter and biogenic silica in deep water below the carbonate compensation depth. Argillaceous mudstones deposited during a regional hiatus at the end of the Upper Triassic show unusual Fe and trace metal enrichment, together with a marked positive Ce anomaly, indicative of slow hydrogenous accumulation.The marginal oceanic crustal zone also shows dominantly terrigenous and siliceous biogenic deposition but with the addition of an important hydrothermal component represented by Fe-Mn deposits. These occur within and immediately above the Upper Triassic lavas of the oceanic crust and as intercalations in the overlying Lower Cretaceous radiolarian chert sequence. Most of these sediments show strong Fe-Mn fractionation; several show a negative Ce anomaly implying rapid incorporation of the REEs from seawater.The Upper Triassic Fe-Mn deposits associated with the lavas are relatively trace-element-depleted and record rapid localised precipitation from relatively high-temperature hydrothermal solutions. By contrast, the more manganiferous and trace-element-enriched metalliferous horizons in the Jurassic to Lower Cretaceous chert sequences represent more dilute low-temperature hydrothermal discharge. Regional comparisons suggest that dominantly manganiferous deposits free of sulphides are characteristic of the early formed Mesozoic ocean crust compared with well established spreading axes like the Troodos Massif, Cyprus.  相似文献   

3.
Ocean anoxia has been widely implicated in the Permian-Triassic extinction.However,the duration and distribution of the ocean anoxia remains controversial.In this study,the detailed redox changes across the Permian-Triassic boundary(PTB)in the shallow platform interior at Great Bank of Guizhou(GBG)has been reconstructed based on the high-resolution microfossil composition and multiple paleo-redox proxies.The shallow platform is characterized by low sulfur(total sulfur(TS)and pyrite sulfur(Spy))concentrations,low Spy/TOC ratios,and low DOP values before the mass extinction,representing oxic conditions well.Following the mass extinction,the shift of multiple geochemical proxies,including high Spy/TOC ratios and DOP values,indicates dysoxic-anoxic conditions in shallow ocean.Furthermore,we reconstruct the transition of the redox conditions of Nanpanjiang Basin:the intense volcanic eruptions,which release huge CO2 and SO2 before the mass extinction,provoke the temperature rising and the collapse of terrestrial ecosystem.As a result,the increased weathering influx causes the carbon isotopic negative excursion and the expansion of the ocean oxygen minimum zone(OMZ).When the OMZ expanded into the photic zone,the episodic H2S release events enhance the pyrite burial at Dajiang section.Thus,intense volcanic eruptions,temperature increase,and oceanic hypoxia together lead to the PTB extinction.Recent studies show high temperature might be the key mechanism of the PTB extinction.In addition,this study confirms that the microbialites were formed in the dysoxicanoxic shallow water.  相似文献   

4.
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.  相似文献   

5.
The Ediacaran Doushantuo Formation with well-preserved fossil record in South China provides a rare window for our understanding of biological evolution,global carbon cycle,and oceanic redox states.Prominent negativeδ~(13)C anomalies(i.e.,the Shuram excursion)in Ediacaran successions worldwide fundamentally challenge the traditional models of isotopic mass balance.Additionally,conflicting opinions of both oxic and anoxic conditions have been proposed for the deep waters during this period.Here,we present a detailed study of pyrite morphology and carbonate carbon isotope data documented from drill core samples at Songtao County,northeastern Guizhou.Framboid aggregates are the dominant pyrite form in black shale and they can transfer to euhedral crystals through continuous growth of the constituent microcrystals.A positive correlation between microcrystal sizes(d)and framboid diameters(D)is observed,while the different D/d ratios of framboids in argillaceous dolostone and black shale reflect different substrate availability.Electron microprobe analyses reveal no consistent compositional patterns between framboidal and euhedral pyrites.Framboid size distributions of the investigated drill core,in combination with previously published redox data from the intra-shelf Jiulongwan section,shelf margin Zhongling section,and lower slope Wuhe section,suggest that three episodes of marine euxinia have been established throughout the deposition of the Doushantuo Formation.The time lag between the uppermost euxinic interval and the Shuram excursion may arise from the depression of sulfate reduction maintained by other oxidants.  相似文献   

6.
Here we report a detailed trace element study of the cherts from Liuchapo Formation, which is a terminal Ediacaran (551-542 Ma) succession in South China deposited in deep-water basinal setting. The REE of Liuchapo cherts shows similar features as observed for anoxic modern seawater (but not for hydrothermal fluids), characterized by positive La anomaly (LaN/CeN = 0.83–1.91, average 1.37), moderately negative Ce anomaly (0.53–1.1, average 0.73), positive Gd anomaly (average 1.08), positive Y anomaly (average 1.21), and depleted LREE and MREE. In addition, the Liuchapo cherts have low ΣREE (3.36–56.13 ppm, average 20.6 ppm), low Al2O3, Ti, Th and Zr concentrations, and high Y/Ho ratios (up to 43.9). The redox-sensitive trace elements concentrations in the cherts do not correlate with detrital input proxies. All of these features suggest that the redox-sensitive trace elements in the cherts were authigenically concentrated in water column and their concentrations thus are excellent indicators of ancient redox conditions. Very low Th/U ratios, high V/(V+Ni) and Fe⊤/Al ratios, enrichments of redox-sensitive trace elements (U, V, Mo), and low concentration of Mn in the cherts imply anoxia in the deep seawater. Our data reveal that the terminal Ediacaran ocean was not completely oxidized and the deep ocean was still anoxic, at least in South China. We propose that although the oxidative events existed in the terminal Ediacaran oceans, decomposition of organic matter prolonged anoxia in the deep ocean. Supported by National Natural Science Foundation of China (Grants Nos. 40532012, 40873007, 40603021) and Chinese Academy of Sciences (Grant No. KZCX3-SW-141)  相似文献   

7.
Ocean Drilling Program (ODP) Hole 504B near the Costa Rica Rift is the deepest hole drilled in the ocean crust, penetrating a volcanic section, a transition zone and a sheeted dike complex. The distribution of Li and its isotopes through this 1.8-km section of oceanic crust reflects the varying conditions of seawater alteration with depth. The upper volcanic rocks, altered at low temperatures, are enriched in Li (5.6-27.3 ppm) and have heavier isotopic compositions (δ7Li=6.6-20.8‰) relative to fresh mid-ocean ridge basalt (MORB) due to uptake of seawater Li into alteration clays. The Li content and isotopic compositions of the deeper volcanic rocks are similar to MORB, reflecting restricted seawater circulation in this section. The transition zone is a region of mixing of seawater with upwelling hydrothermal fluids and sulfide mineralization. Li enrichment in this zone is accompanied by relatively light isotopic compositions (−0.8-2.1‰) which signify influence of basalt-derived Li during mineralization and alteration. Li decreases with depth to 0.6 ppm in the sheeted dike complex as a result of increasing hydrothermal extraction in the high-temperature reaction zone. Rocks in the dike complex have variable isotopic values that range from −1.7 to 7.9‰, depending on the extent of hydrothermal recrystallization and off-axis low-temperature alteration. Hydrothermally altered rocks are isotopically light because 6Li is preferentially retained in greenschist and amphibolite facies minerals. The δ7Li values of the highly altered rocks of the dike complex are complementary to those of high-temperature mid-ocean ridge vent fluids and compatible to equilibrium control by the alteration mineral assemblage. The inventory of Li in basement rocks permits a reevaluation of the role of oceanic crust in the budget of Li in the ocean. On balance, the upper 1.8 km of oceanic crusts remains a sink for oceanic Li. The observations at 504B and an estimated flux from the underlying 0.5 km of gabbro suggest that the global hydrothermal flux is at most 8×109 mol/yr, compatible with geophysical thermal models. This work defines the distribution of Li and its isotopes in the upper ocean crust and provides a basis to interpret the contribution of subducted lithosphere to arc magmas and cycling of crustal material in the deep mantle.  相似文献   

8.
The osmium (Os) concentration and187Os/186Os ratio of several recent, marine, organic-rich sediment samples from three widely separated sites have been measured. Os concentrations range from 0.095 to 0.212 ppb and187Os/186Os ratios range from 8.2 to 8.9. The calculated fraction of hydrogenous Os exceeds 78% in all samples. Thus, the187Os/186Os ratio of these samples reflects Os isotopic composition of seawater. The small range in measured187Os/186Os ratio indicates that the Os isotopic composition at these sites is fairly homogeneous. The large magnitude of the Os burial flux at these sites indicates the Os burial in association with organic-rich sediments is an important sink in the marine cycle of Os. These data also suggest that ancient organic-rich sediments may provide a record of past variations in the Os isotopic composition of seawater.  相似文献   

9.
Hafnium and Nd isotopes are increasingly used as paleoceanographic proxies. Comparing the “mantle–crust array” and the “seawater array” in plots of εHf vs. εNd, it has been observed that for a given εNd value the corresponding εHf value is higher for seawater than it is for terrestrial rocks. While this difference had initially been explained by significant hydrothermal input of mantle Hf into seawater, the currently favoured explanation is incongruent weathering of continental rocks producing radiogenic riverine Hf input.We here address this topic from the perspective of the behaviour of these two elements in seawater and in ferromanganese (Fe–Mn) crusts. We distinguish between a “truly dissolved” and a “dissolved” Hf and Nd pool, the latter being comprised of truly dissolved and colloid-bound (“colloidal”) Hf and Nd. While there exists a hydrothermal pathway for colloid-bound dissolved mantle Hf into the oceans, there is, in marked contrast to Nd, no important riverine pathway for colloidal or truly dissolved continental Hf. Owing to their respective chemical speciation in seawater, there exists truly dissolved Nd in the ocean, while the amount of truly dissolved Hf is insignificant.Neodymium is in exchange equilibrium between local seawater and both, the hydrous Fe and Mn oxides hydrogenetic Fe–Mn crusts are composed of. Due to continuous ad- and desorption there is continuous isotopic re-equilibration and the isotopic composition of Nd in a Fe–Mn crust reflects that of truly dissolved Nd in local ambient seawater. In contrast, Hf is only associated with the hydrous Fe oxides on which it forms surface precipitates that do not exchange with seawater. Due to this lack of isotopic re-equilibration, the isotopic composition of Hf in a Fe–Mn crust is the average of that of all the Hf scavenged during the lifetime of the hydrous Fe oxide particles. Since the Hf-bearing hydrous Fe oxides in a Fe–Mn crust do not form from local ambient seawater at the crust's growth site but are advected as colloids or fine particles, their Hf isotopic composition depends on the origin and migration pathway of these colloids. Hence, while Nd isotopes in Fe–Mn crusts provide reliable information on truly dissolved Nd in local ambient seawater, Hf isotopes rather indicate the origin and pathway of hydrous Fe oxide colloids, and might differ from truly dissolved Hf in local ambient seawater. This may explain the occasional decoupling of Nd and Hf isotopes in Fe–Mn crusts and supports the notion of a significant hydrothermal mantle signal of Hf in seawater.  相似文献   

10.
The stable isotope systems of the transition metals potentially provide constraints on the current and past operation of the biological pump,and on the state of ocean redox in Earth history.Here we focus on two exemplar metals,nickel(Ni)and zinc(Zn).The oceanic dissolved pool of both elements is isotopically heavier than the known inputs,implying an output with light isotope compositions.The modern oceanic cycle of both these elements is dominated by biological uptake into photosynthesised organic matter and output to sediment.It is increasingly clear,however,that such uptake is associated with only very minor isotope fractionation.We suggest that the isotopic balance is instead closed by the sequestration of light isotopes to sulphide in anoxic and organic-rich sediments,so that it is ocean chemistry that controls these isotope systems,and suggesting a different but equally interesting array of questions in Earth history that can be addressed with these systems.  相似文献   

11.
Among long-lived radioactive parent-daughter element pairs, the ratio Lu/Hf is strongly fractionated relative to constant Sm/Nd in the Earth's sedimentary system. This is caused by high resistance to chemical weathering of the mineral zircon (Zr,Hf)SiO4. Zircon-bearing sandy sediments on and near continents have very low Lu/Hf, while deep-sea clays have up to three times the chondritic Lu/Hf ratio. Turbidity currents mechanically carry the low-Lu/Hf sandy material onto the ocean floor. The results are important for the crust-to-mantle recycling discussion, where most recycled materials would be subducted oceanic sediments. Such sediment should be capable of explaining the HfNd mantle isotopic variation by mixing with peridotite, but in fact any average pelagic sediment has Nd/Hf and Lu/Hf too high to allow mixing curves to pass through the Hf/Nd isotopic array. The array could only be reproduced by subduction of turbidite sandstone with pelagic sediment in the approximate ratio 1.2 to 1, and by maintaining a good mixture between the two components. At least today, turbidites are available for subduction only at locations quite different and distant from those where pelagic sediments may be recycled; furthermore, mantle isotopic variation shows that the mantle often cannot mix itself well enough to homogenize these widely-separated sedimentary components to the degree required. The Lu/Hf fractionations place a severe restriction on the ability of recycled sediments to explain mantle isotopic patterns.  相似文献   

12.
Understanding the origin of ocean island basalts(OIB) has important bearings on Earth's deep mantle.Although it is widely accepted that subducted oceanic crust, as a consequence of plate tectonics, contributes material to OIB's formation, its exact fraction in OIB's mantle source remains ambiguous largely due to uncertainties associated with existing geochemical proxies. Here we show, through theoretical calculation, that unlike many known proxies, triple oxygen isotope compositions(i.e.D^(17 )O) in olivine samples are not affected by crystallization and partial melting. This unique feature, therefore, allows olivine D^(17 )O values to identify subducted oceanic crusts in OIB's mantle source. Furthermore, the fractions of subducted ocean sediments and hydrothermally altered oceanic crust in OIB's mantle source can be quantified using their characteristic D^(17 )O values. Based on published D^(17 )O data, we estimated the fraction of subducted oceanic crust to be as high as 22.3% in certain OIB, but the affected region in the respective mantle plume is likely to be limited.  相似文献   

13.
Adsorption studies with sediment from the Bay of Quinte (Lake Ontario) indicate that the adsorption isotherm for sulfate concentration greater than 20 mg/l can be described by a Langmuir-type equation. The accompanying changes in δ34S of the solutions range from +0.9 to +6.0‰ indicating enrichment of32S in the sediments. The corresponding isotopic fractionation between the adsorbed sulfate and the sulfate remaining in solution ranges from ?10 to ?24‰, the larger fractionations being associated with low sulfate concentrations. The adsorbed sulfate is shown to significantly afftect the isotopic composition of the sediment in contact with the sulfate-bearing solution. The desorption of adsorbed sulfate is considered a possible mechanism for enriching natural freshwaters with32S.  相似文献   

14.
himu, em i andem ii are three of the main geochemical mantle components that give rise to oceanic island basalts [1]. They represent the end members that produce the extreme isotopic compositions measured on intraplate volcanics. In French Polynesia, all three mantle components are represented in volcanic rocks. The characteristichimu signature is found in Tubuai, Mangaia and Rurutu,em i is present in the source of Rarotonga and Pitcairn volcanics andem ii dominates the composition of most Society Islands. Intermediate values between the three end members are found on most islands.We suggest that the three components are not independent but are physically related in the mantle. Thehimu component is thought to be recycled oceanic crust that lost part of its Pb through hydrothermal processes prior to and during subduction.em i andem ii are believed to acquire their isotopic and trace element characteristics through entrainment of sediments that were subducted together with the oceanic crust.The trace element pattern and the isotopic composition ofhimu lavas can be quantitatively modelled using a mixture of 25% old recycledmorb crust and 75% mantle peridotite. The extreme Pb composition is modelled assuming that Pb was lost from oceanic crust when hydrothermal alteration at the ridge leached Pb from the basalt to redeposit it as sulphides on top of and throughout the crust, followed by preferential dissolution of sulphides during dehydration in the subduction zone. These processes led to a drastic increase of theU/Pb ratio of the subducted material which evolved over 2 Ga to very radiogenic Pb isotopic compositions. Pb isotopic compositions similar to those ofem i andem ii are modelled assuming that sediments with average crustal Pb isotopic compositions were subducted and recycled into the mantle together with the underlyingmorb oceanic crust. Pelagic sediments (μ 5 andκ 6) account for the Pb isotopic composition ofem i whereas terrigenous sediments (μ 10 andκ 4.5) evolve towards theem ii end member. A few percent of sediment in the recycled crust-sediment mixture will destroy the characteristic Pb isotopic signature of thehimu component. This, together with the low probability of isolating oceanic crust in the mantle for 2 Ga, explains why the extremehimu composition, as seen on Tubuai and St Helena, is sampled so rarely by oceanic volcanism.  相似文献   

15.
The87Sr/86Sr ratio of seawater strontium (0.7091) is less than the87Sr/86Sr ratio of dissolved strontium delivered to the oceans by continental run-off (～0.716). Isotope exchange with strontium isotopically lighter oceanic crust during hydrothermal convection within spreading oceanic ridges can explain this observation. In quantitative terms, the current87Sr/86Sr ratio of seawater (0.7091) may be maintained by balancing the continental run-off flux of strontium (0.59 × 1012 g/yr) against a hydrothermal recirculation flux of 3.6 × 1012 g/yr, during which the87Sr/86Sr ratio of seawater drops by 0.0011. A concomitant mean increase in the87Sr/86Sr ratio of the upper 4.5 km of oceanic crust of 0.0010 (0.7029–0.7039) should be produced. This required87Sr enrichment has been observed in hydrothermally metamorphosed ophiolitic rocks from the Troodos Massif, Cyprus.The post-Upper Cretaceous increase in the strontium isotopic composition of seawater(～0.7075–0.7091) covaries smoothly with inferred increase in land area. This suggests that during this period the main factor which has caused variability in the87Sr/86Sr ratio of seawater strontium could have been variation in the magnitude of the continental run-off flux caused by variation in land area. Variations in land area may themselves have been partly a consequence of variations in global mean sea-floor spreading rate.  相似文献   

16.
On the basis of a dynamic model of a continuous Pb isotope evolution, the variations in the isotopic ratios of uranogenic and thorogenic Pb in a number of young ore deposits, ocean sediments and volcanic rocks from mid-ocean ridges, oceanic islands, island arcs and continents are evaluated. The deviations in the Th/U ratio from its model values are calculated. A model parameterT which indicates a more ancient enrichment in U/Pb (crustal-type Pb sources) or younger enrichment in U/Pb (mantle-type Pb sources) is also calculated. The relative change in the Th/U ratio is close to 1 for mantle-type Pb sources (lowerT values) and decreases for crustal-type Pb sources (higherT values). An interpretation of these changes could be connected with the differences in the U and Th geochemical behaviours in metamorphic processes under the conditions of a deeper (mantle) or crustal source owing to the differences in their valence states. In some cases they have similar (U4+ and Th4+) migration abilities; in others (U6+ and Th4+), considerably different.  相似文献   

17.
High-pressure experiments on a natural pelite have been conducted at 2–11-GPa pressures in order to evaluate contributions of subducted sediments to arc and ocean island magmatism. Obtained phase relations suggest that, at least in modern subduction zones, subsolidus dehydration of chlorite and phengitic muscovite in the subducted sediments, rather than partial melting, is a predominant process in overprinting sediment components onto the magma source region. Trace element compositions of sediment-derived fluids are estimated based on dehydration experiments at 5.5 GPa and 900/1300°C. Pb is effectively transported by fluids relative to other elements. This results in the Pb enrichment for arc basalts by fluids, generated by the dehydration of subducted sediments, together with altered mid-ocean ridge basalt (MORB), and complementary depletion of Pb in subducted sediments. Inferred arc magma compositions obtained by model calculations based on the present experimental results agree well with a natural primitive arc basalt composition. A large increase in the U/Pb ratio in the subducted sediments at deeper levels than major dehydration depths results in a high Pb isotopic ratio through radioactive decay after long periods of isolation. Combined with other isotopic ratios such as Sr and Nd, it is possible to produce the EM II source, one of the enriched geochemical reservoirs for ocean island basalt magmas, by mixing of a small amount of subducted sediments with depleted or primitive mantle.  相似文献   

18.
We report new187Os/186Os data and Re and Os concentrations in metalliferous sediments from the Pacific to construct a composite Os isotope seawater evolution curve over the past 80 m.y. Analyses of four samples of upper Cretaceous age yield187Os/186Os values of between 3 and 6.5 and187Re/186Os values below 55. Mass balance calculations indicate that the pronounced minimum of about 2 in the Os isotope ratio of seawater at the K-T boundary probably reflects the enormous input of cosmogenic material into the oceans by the K-T impactor(s). Following a rapid recovery to187Os/186Os of 3.5 at 63 Ma, data for the early and middle part of the Cenozoic show an increase in187Os/186Os to about 6 at 15 Ma. Variations in the isotopic composition of leachable Os from slowly accumulating metalliferous sediments show large fluctuations over short time spans. In contrast, analyses of rapidly accumulating metalliferous carbonates do not exhibit the large oscillations observed in the pelagic clay leach data. These results together with sediment leaching experiments indicate that dissolution of non-hydrogenous Os can occur during the hydrogen peroxide leach and demonstrate that Os data from pelagic clay leachates do not always reflect the Os isotopic composition of seawater.

New data for the late Cenozoic further substantiate the rapid increase in the187Os/186Os of seawater during the past 15 Ma. We interpret the correlation between the marine Sr and Os isotope records during this time period as evidence that weathering within the drainage basin of the Ganges-Brahmaputra river system is responsible for driving seawater Sr and Os toward more radiogenic isotopic compositions. The positive correlation between87Sr/86Sr and U concentration, the covariation of U and Re concentrations, and the high dissolved Re, U and Sr concentrations found in the Ganges-Brahmaputra river waters supports this interpretation. Accelerating uplift of many orogens worldwide over the past 15 Ma, especially during the last 5 Ma, could have contributed to the rapid increase in187Os/186Os from 6 to 8.5 over the past 15 Ma. Prior to 15 Ma the marine Sr and Os record are not tightly coupled. The heterogeneous distribution of different lithologies within eroding terrains may play an important role in decoupling the supplies of radiogenic Os and Sr to the oceans and account for the periods of decoupling of the marine Sr and Os isotope records.  相似文献   


19.
Chemical data presented in this paper indicate a good correlation between P2O5 and Fe2O3 in some iron-rich volcanogenic sediments from the East Pacific Rise. In addition, adsorption experiments and chemical analyses of deuterically altered and unaltered samples of submarine basalts strongly suggest that this association is due to the reaction of phosphate in sea water with poorly crystallized hydrous ferric oxides. East Pacific Rise sediments adsorb far greater amounts of phosphate from sea water than either carbonate or non-carbonate sediments from other areas of the ocean. From geochemical flux calculations it is concluded that an appreciable proportion of dissolved phosphate delivered to the oceans by rivers is removed by ridge crest volcanogenic iron oxides either as absorbed surface coatings or as discrete, but highly disordered, ferric phosphate phases. This process should be taken into consideration when considering oceanic phosphate budgets, both in the present and past oceans.  相似文献   

20.
A double-spike method was used to obtain Mo isotope data for sediments and waters of the seasonally anoxic Chesapeake Bay, and its primary tributary, the Susquehanna River. The dissolved Mo distribution in the estuary is non-conservative, reflecting minor Mo loss to the sediments, although removal of Mo to the sediments does not have a large influence on the isotopic composition of the water column. The δ98Mo of dissolved Mo in most of the estuary is dominated by seawater. Six samples with salinity > 15 have an average δ98Mo = + 2.17‰ (± 0.12), which agrees well with a δ98Mo value for the CASS-4 seawater standard of + 2.23‰. A single sample of Susquehanna River water has a δ98Mo of + 1.02‰, consistent with recent findings of positive δ98Mo in rivers worldwide. Susquehanna river sediments, in contrast, have δ98Mo ～ ? 0.1‰. The difference between the river water and sediment values implies that isotopic fractionation occurs within the river basin. The δ98Mo values for estuarine sediments are offset from values in the overlying water. Most samples deposited before 1925 have δ98Mo less than 0‰, similar to the Susquehanna sediments. Subsequently, there is an increase in the variability of δ98Mo, with values ranging up to + 0.8‰. The transition to increased variability coincides with the onset of authigenic Mo deposition, which was previously attributed to escalating summertime anoxia. Authigenic Mo concentrations correlate poorly with δ98Mo in core samples, suggesting that independent mechanisms influence the two parameters. Authigenic Mo concentrations may be controlled by shifting pore water H2S levels, while δ98Mo may be primarily affected by annual variations in Mn refluxing.  相似文献   

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