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1.
The contribution of soil organic matter (SOM) to continental margins is largely ignored in studies on the carbon budget of marine sediments. Detailed geochemical investigations of late Quaternary sediments (245-0 ka) from the Niger and Congo deep-sea fans, however, reveal that Corg/Ntot ratios and isotopic signatures of bulk organic matter (δ13Corg) in both fans are essentially determined by the supply of various types of SOM from the river catchments thus providing a fundamentally different interpretation of established proxies in marine sciences. On the Niger fan, increased Corg/Ntot and δ13Corg (up to −17‰) were driven by generally nitrogen-poor but 13C-enriched terrigenous plant debris and SOM from C4/C3 vegetation/Entisol domains (grass- and tree-savannah on young, sandy soils) supplied during arid climate conditions. Opposite, humid climates supported drainage of C3/C4 vegetation/Alfisol/Ultisol domains (forest and tree-savannah on older/developed, clay-bearing soils) that resulted in lower Corg/Ntot and δ13Corg (< −20‰) in the Niger fan record. Sediments from the Congo fan contain a thermally stable organic fraction that is absent on the Niger fan. This distinct organic fraction relates to strongly degraded SOM of old and highly developed, kaolinite-rich ferallitic soils (Oxisols) that cover large areas of the Congo River basin. Reduced supply of this nitrogen-rich and 12C-depleted SOM during arid climates is compensated by an elevated input of marine OM from the high-productive Congo up-welling area. This climate-driven interplay of marine productivity and fluvial SOM supply explains the significantly smaller variability and generally lower values of Corg/Ntot and δ13Corg for the Congo fan records. This study emphasizes that ignoring the presence of SOM results in a severe underestimation of the terrigenous organic fraction leading to erroneous paleoenvironmental interpretations at least for continental margin records. Furthermore, burial of SOM in marine sediments needs more systematic investigation combining marine and continental sciences to assess its global relevance for long-term sequestration of atmospheric CO2.  相似文献   

2.
The geochemistry of Upper Quaternary organic-rich (Corg 3.7–10.0%) sediments recovered by the 40-m-long Core MD02-2508 from the upper continental slope of Baja California is compared to the chemical composition of sedimentary rocks from the Miocene Monterey Formation, California. It is ascertained that concentrations of most macroelements (Al, Ti, Mg, K, Fe, M, S, Corg) and many microelements, including chalcophiles Ag, As, Mo, Sb, Se, Zn, along with some others (U, Co, Ni, Y, and REE) are nearly equal in both types of sediments. In addition, concentrations of most microelements in both types of sediments are close, to the average values common for the worldwide carbonaceous black shales irrespective of their lithology and age, indicating a stable influence of organic matter on their concentration during sedimentation and early digenesis.  相似文献   

3.
Geochemical and isotopic data for the uppermost 1.2 m of the sediments of the central Santa Monica Basin plain were examined to better understand organic matter deposition and recycling at this site. Isotopic signatures (Δ14C and δ13C) of methane (CH4) and dissolved inorganic carbon (DIC) indicate the occurrence of anaerobic oxidation of CH4 that is fueled by CH4 supplied from a relict reservoir that is decoupled from local organic carbon (Corg) degradation and methanogenesis. This finding was corroborated by a flux budget of pore-water solutes across the basal horizon of the profile. Together these results provide a plausible explanation for the anomalously low ratio between alkalinity production and sulfate consumption reported for these sediments over two decades ago. Shifts in Δ14C and δ13C signatures of Corg have previously been reported across the 20-cm depth horizon for this site and attributed to a transition from oxic to anoxic bottom water that occurred ~350 years BP. However, we show that this horizon also coincides with a boundary between the base of a hemipelagic mud section and the top of a turbidite interval, complicating the interpretation of organic geochemical data across this boundary. Radiocarbon signatures of DIC diffusing upward into surface sediments indicate that remineralization at depth is supported by relatively 14C-enriched Corg within the sedimentary matrix. While the exact nature of this Corg is unclear, possible sources are hemipelagic mud sections that were buried rapidly under thick turbidites, and 14C-rich moieties dispersed within Corg-poor turbidite sections.  相似文献   

4.

Selenium is one of the most important minor elements in massive sulfide ores. This study focuses on selenium minerals present in the oxidation zone of the Yubeleinoe massive sulfide deposit, the South Urals, Russia: clausthalite (PbSe), tiemannite (HgSe), and naumannite (Ag2Se). These minerals are associated with goethite and siderite. Thermodynamic modeling was used to estimate the physicochemical parameters of selenide stability and the possible formation of Pb, Hg, and Ag selenites as a result of sulfide ore oxidation. The Eh–pH diagrams for the Fe–S–CO2–H2O and Fe–Se–CO2–H2O systems were calculated to estimate the physicochemical formation conditions of the Yubileinoe oxidation zone, as well as for the M–Se–Н2О and M–S–H2O (M = Hg, Pb, Ag) systems. The physicochemical parameters of clausthalite, naumannite, and tiemannite stability are consistent with these conditions. Only the formation of PbSeO3 is theoretically possible among Pb, Ag, and Hg selenites.

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5.
A multicomponent diagenetic model was developed and applied to reconstruct the conditions under which the most recent sapropel, S1, was deposited in the eastern Mediterranean Sea. Simulations demonstrate that bottom waters must have been anoxic and sulphidic during the formation of S1 and that organic matter deposition was approximately three times higher than at present. Nevertheless, most present day sediment and pore water profiles — with the exception of pyrite, iron oxyhydroxides, iron-bound phosphorus and phosphate — can be reproduced under a wide range of redox conditions during formation of S1 by varying the depositional flux of organic carbon. As a result, paleoredox indicators (e.g., Corg:S ratio, Corg:Porg ratio, trace metals) are needed when assessing the contribution of oxygen-depletion and enhanced primary production to the formation of organic-rich layers in the geological record. Furthermore, simulations show that the organic carbon concentration in sediments is a direct proxy for export production under anoxic bottom waters.The model is also used to examine the post-depositional alteration of the organic-rich layer focussing on nitrogen, phosphorus, and organic carbon dynamics. After sapropel formation, remineralisation is dominated by aerobic respiration at a rate that is inversely proportional to the time since bottom waters became oxic once again. A sensitivity analysis was undertaken to identify the most pertinent parameters in regulating the oxidation of sapropels, demonstrating that variations in sedimentation rate, depositional flux of organic carbon during sapropel formation, bottom water oxygen concentration, and porosity have the largest impact. Simulations reveal that sedimentary nutrient cycling was markedly different during the formation of S1, as well as after reoxygenation of bottom waters. Accumulation of organic nitrogen in sediments doubled during sapropel deposition, representing a significant nitrogen sink. Following reventilation of deep waters, N2 production by denitrification was almost 12 times greater than present day values. Phosphorus cycling also exhibits a strong redox sensitivity. The benthic efflux of phosphate was up to 3.5 times higher during the formation of S1 than at present due to elevated depositional fluxes of organic matter coupled with enhanced remineralisation of organic phosphorus. Reoxygenation of bottom waters leads to a large phosphate pulse to the water column that declines rapidly with time due to rapid oxidation of organic material. The oxidation of pyrite at the redox front forms iron oxyhydroxides that bind phosphorus and, thus, attenuate the benthic phosphate efflux. These results underscore the contrasting effects of oxygen-depletion on sedimentary nitrogen and phosphorus cycling. The simulations also confirm that the current conceptual paradigm of sapropel formation and oxidation is valid and quantitatively coherent.  相似文献   

6.
Iodine is characteristically enriched at the surface of hemipelagic and nearshore sediments deposited under oxygenated conditions. In such sediments, bulk I/Corg ratios usually decrease with depth to values which are characteristic of anoxic sediments, reflecting a preferential release of I during early diagenesis. There is some debate as to whether sedimentary I is associated with the iron oxyhydroxide phase or with the organic fraction, and whether the decrease in I/Corg with depth is due to the dissolution of the iron oxyhydroxides or the decomposition of labile organic matter.It is shown that in a surficial hemipelagic sediment sample and in a nearshore sediment core I is mainly associated with the organic fraction and, moreover, that humic substances are involved in the surficial iodine enrichment. Laboratory experiments on the uptake and release of I by and from sedimentary humic substances also suggest a mechanism whereby humic materials reduce iodate at the sediment/water interface to an electrophilic I species which further reacts with the organic matter to produce iodinated organic molecules. During burial, this excess I could be displaced from the organic matrix by nucleophiles such as sulphide ions or thiosulphate, thus providing a possible explanation for the decrease in I/Corg ratio with depth observed in many nearshore and hemipelagic sediments.  相似文献   

7.
Geochemistry of Peruvian near-surface sediments   总被引：6，自引：0，他引：6  
Sixteen short sediment cores were recovered from the upper edge (UEO), within (WO) and below (BO) the oxygen minimum zone (OMZ) off Peru during cruise 147 of R/V Sonne. Solids were analyzed for major/trace elements, total organic carbon, total inorganic carbon, total sulfur, the stable sulfur isotope composition (δ34S) of pyrite, and sulfate reduction rates (SRR). Pore waters were analyzed for dissolved sulfate/sulfide and δ34S of sulfate. In all cores highest SRR were observed in the top 5 cm where pore water sulfate concentrations varied little due to resupply of sulfate by sulfide oxidation and/or diffusion of sulfate from bottom water. δ34S of dissolved sulfate showed only minor downcore increases. Strong 32S enrichments in sedimentary pyrite (to −48‰ vs. V-CDT) are due to processes in the oxidative part of the sulfur cycle in addition to sulfate reduction. Manganese and Co are significantly depleted in Peruvian upwelling sediments most likely due to mobilization from particles settling through the OMZ, whereas release of both elements from reducing sediments only seems to occur in near-coastal sites. Cadmium, Mo and Re are exceptionally enriched in WO sediments (<600 m water depth). High Re and moderate Cd and Mo enrichments are seen in BO sediments (>600 m water depth). Re/Mo ratios indicate anoxic and suboxic conditions for WO and BO sediments, respectively. Cadmium and Mo downcore profiles suggest considerable contribution to UEO/WO sediments by a biodetrital phase, whereas Re presumably accumulates via diffusion across the sediment-water interface to precipitation depth. Uranium is distinctly enriched in WO sediments (due to sulfidic conditions) and in some BO sediments (due to phosphorites). Silver transfer to suboxic BO sediments is likely governed by diatomaceous matter input, whereas in anoxic WO sediments Ag is presumably trapped due to sulfide precipitation. Cadmium, Cu, Zn, Ni, Cr, Ag, and T1 predominantly accumulate via biogenic pre-concentration in plankton remains. Rhenium, Sb, As, V, U and Mo are enriched in accordance with seawater TE availability. Lead and Bi enrichment in UEO surface sediments is likely contributed by anthropogenic activity (mining). Accumulation rates of TOC, Cd, Mo, U, and V from Peruvian and Namibian sediments exceed those from the Oman Margin and Gulf of California due to enhanced preservation off Peru and Namibia.  相似文献   

8.
We investigated the phosphorus (P) and iron (Fe) fractionation in four cores with anoxic sediments, deposited during the mid-Cretaceous oceanic anoxic event 2 (∼94 Ma) and the Paleocene-Eocene thermal maximum (∼55 Ma), that were exposed to oxygen after core recovery. Surprisingly, P associated with iron oxyhydroxides (Fe-bound P) was a major P phase in these laminated sediments deposited under euxinic conditions. A significant fraction of total Fe was present as (poorly) crystalline ferric Fe. This fraction increased with increasing storage time of the investigated cores. In carbonate-poor samples, Fe-bound P accounted for up to 99% of total P and its abundance correlated with pyrite contents. In samples with higher CaCO3 contents (>5 wt% in the investigated samples), P was mostly present in authigenic Ca-P minerals, irrespective of pyrite contents. We conclude that the P fractionation in anoxic, carbonate-poor, sediments is strongly affected by pyrite oxidation that occurs when these sediments are exposed to oxygen. Pyrite oxidation produces sulfuric acid and iron oxyhydroxides. The abundance of poorly crystalline Fe oxyhydroxides provides further evidence that these were indeed formed through recent (post-recovery) oxidation rather than in situ tens of millions of years ago. The acid dissolves apatite and the released phosphate is subsequently bound in the freshly formed iron oxyhydroxides. Pyrite oxidation thus leads to a conversion of authigenic Ca-P to Fe-bound P. In more calcareous samples, CaCO3 can act as an effective buffer against acidic dissolution of Ca-P minerals. The results indicate that shielding of sediments from atmospheric oxygen is vital to preserve the in situ P fractionation and to enable a valid reconstruction of marine phosphorus cycling based on sediment records.  相似文献   

9.
Published and original data on the contents of 50 elements in carbonaceous sediments from seas (Black, Baltic, and Caspian) and fertile oceanic shelves (shelves of Namibia, Peru, Chile, and California) are generalized. The comparison of these results with the average composition of ancient carbonaceous shales reveals both similarities and differences in the distribution of indicator trace elements (Re, Hg, Se, Ag, Cd, Tl, U, Mo, As, Ni, and Zn). Correlation coefficients were analyzed to determine the characteristic element associations. It is established that oceanic carbonaceous sediments are closer in composition to carbonaceous shales than their marine analogues, which is related to the differences in sedimentation conditions, including hydrological, hydrochemical, and biogeochemical factors. The role of anoxic environment in the accumulation of chalcophile elements in sediments is estimated. The comparison of the contents of some mobile trace elements in oceanic water and carbonaceous sediments of modern oceans demonstrates that the water composition affects the composition of carbonaceous sediments and can be used for deciphering the composition of ancient ocean water.  相似文献   

10.
Some comparative marine chemistries of rhenium, gold, silver and molybdenum   总被引：1，自引：0，他引：1  
Four metals, Re, Au, Ag and Mo, whose dissolved forms in seawater can potentially be reduced to insoluble states, have been measured in a variety of solids depositing under anoxic conditions: hydrothermal sulfides; coastal sediments; and phosphorites. For comparative purposes these elements have also been determined in ferromanganese minerals and pelagic sediments which have accumulated under oxidizing conditions. Rhenium appears to be a unique sentinel for identifying reducing depositional environments, where enrichments of greater than three orders of magnitude above crustal concentrations are found. Molybdenum follows Re in these sediments but Mo is enriched also in those that accumulate under oxidizing conditions. The reported Mo crustal concentrations appear low in comparison to our measured sedimentary values. Gold and Ag are concentrated in hydrothermal deposits and sulfides appear to be involved in the precipitation of these elements. Coastal sediments adjacent to a domestic outfall of Los Angeles, California contain extraordinary high accumulations of anthropogenic Au, Ag and Pt. The study seeks an understanding of the mobilities and sinks of these metals in the marine environment during the major weathering cycle. Further, anthropogenic contributions to their sedimentary concentrations are identified.  相似文献   

11.
We use the evolution of river sediment characteristics and sedimentary Corg from the Himalayan range to the delta to study the transport of Corg in the Ganga-Brahmaputra system and especially its fate during floodplain transit.A detailed characterisation of both mineral and organic particles for a sampling set of river sediments allows taking into account the sediment heterogeneity characteristic of such large rivers. We study the relationships between sediment characteristics (mineralogy, grain size, specific area) and Corg content in order to evaluate the controls on Corg loading. Contributions of C3 and C4 plants are estimated from Corg stable isotopic composition (δ13Corg). We use the evolution of δ13Corg values from the Himalayan range to the delta in order to study the fate of Corg during floodplain transit.Ganga and Brahmaputra sediments define two distinct linear relations with specific area. In spite of 4-5 times higher specific area, Ganga sediments have similar Corg content, grain size and mineralogy as Brahmaputra sediments, indicating that specific area does not exert a primary control on Corg loading. The general correlation between the total Corg content and Al/Si ratio indicates that Corg loading is mainly related to: (1) segregation of organic particles under hydrodynamic forces in the river, and (2) the ability of mineral particles to form organo-mineral aggregates.Bed and suspended sediments have distinct δ13Corg values. In bed sediments, δ13Corg values are compatible with a dominant proportion of fossil Corg derived from Himalayan rocks erosion. Suspended sediments from Himalayan tributaries at the outflow of the range have low δ13Corg values (−24.8‰ average) indicating a dominant proportion of C3 plant inputs. In the Brahmaputra basin, δ13Corg values of suspended sediments are constant along the river course in the plain. On the contrary, suspended sediments of the Ganga in Bangladesh have higher δ13Corg values (−22.4‰ to −20.0‰), consistent with a significant contribution of C4 plant derived from the floodplain. Our data indicate that, during the plain transit, more than 50% of the recent biogenic Corg coming from the Himalaya is oxidised and replaced by floodplain Corg. This renewal process likely occurs during successive deposition-erosion cycles and river course avulsions in the plain.  相似文献   

12.
Sediment cores were collected from the Tilbury Tidal Basin in the Thames Estuary to determine the depositional history of metals in the estuary. Profiles of metals in sediments deposited in the lower Thames Estuary show a 30–50% decrease in concentration for Ag, Cd, Cu, Pb, and Zn, and a 70% decrease for Hg in recent decades. Historic depth soundings data showed the decreases in metal concentrations occurred between 1944 and 1966. The decline in sediment metal concentrations has been attributed to reduced inputs to the estuary, following updating of the major sewage treatment works in 1959 and 1963. This is indicated by the through-core distribution of Mn which implies that prior to 1960 the sediments were deposited in anoxic conditions, which subsequently improved. An increase in Mn concentrations observed in one of the cores has been attributed to increases in the dissolved oxygen of the estuarine waters resulting from the increased efficiency of the sewage treatment works.  相似文献   

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14.
The sediments of the Madeira Abyssal Plain, east of Great Meteor Seamount, are dominated by distal turbidite deposition. While the turbidites exhibit a wide compositional range (25–80% CaCO3), individual examples can be correlated over a wide area and are relatively homogenous. Organic C oxidation, by bottom water oxygen, proceeds from the turbidite tops downwards after emplacement in pelagic conditions, and the progress of this oxidation front is marked by a sharp colour contrast in the sediments (Wilsonet al., 1985). In turbidites with Corg ? 0.5%, redistribution of authigenic U occurs to form a concentration peak (4–9 ppm U), just below the oxidation front or colour change. Several tens μg U/cm2 may be mobilised, and in all examples studied ?60% of the remobilised U is relocated into the peak. Following burial by subsequent turbidites, such U concentration peaks are persistent as relict indicators of their extinct oxidation fronts for at least 2 × 105 years. In the case of thin turbidites where labile Corg is almost exhausted, the U peaks may be located in underlying sedimentary units because of their relationship to the oxidation front. A redox mechanism for U peak formation is suggested from these data rather than a complexation with organic matter.  相似文献   

15.
Stable carbon isotope ratios in the organic fraction of surface sediments from the Laptev Sea shelf were analyzed in order to study the modern distribution pattern of terrestrial organic matter. The '13Corg signature of the surface sediments range from -26.6‰ near the coastal margin to -22.8‰ in the north towards the outer shelf. Characterizing the possible sources of organic matter by their '13Corg signature reveals that the terrestrial influence reaches further north in the eastern than in the western Laptev Sea. Downcore records of the '13Corg, measured on three AMS 14C-dated cores from water depths between 46 and 77 m, specify the spatial and temporal changes in the deposition of terrestrial organic matter on the Laptev Sea shelf during the past 12.7 ka. The major depositional changes of terrestrial organic matter occurred between 11 and 7 ka and comprised the main phase of the southward retreat of the coastline and of the river depocenters due to the postglacial sea level rise.  相似文献   

16.
Blue carbon initiatives require accurate monitoring of carbon stocks. We examined sources of variability in seagrass organic carbon (Corg) stocks, contrasting spatial with short temporal scales. Seagrass morphology and sediment Corg stocks were measured from biomass and shallow sediment cores collected in Moreton Bay, Australia. Samples were collected between 2012 and 2013, from a total of 77 sites that spanned a gradient of water turbidity. Environmental measures of water quality between 2000 and 2013 revealed strong seasonal fluctuations from summer to winter, yet seagrass biomass exhibited no temporal variation. There was no temporal variability in Corg stocks, other than below ground biomass stocks were slightly higher in June 2013. Seagrass locations were grouped into riverine, coastal, and seagrass loss locations and short temporal variability of Corg stocks was analysed within these categories to provide clearer insights into temporal patterns. Above ground Corg stocks were similar between coastal and riverine meadows. Below ground Corg stocks were highest in coastal meadows, followed by riverine meadows. Sediment Corg stocks within riverine meadows were much higher than at coastal meadows and areas of seagrass loss, with no difference in sediment Corg stocks between these last two categories. Riverine seagrass meadows, of higher turbidity, had greater total Corg stocks than meadows in offshore areas irrespective of time. We suggest that Corg stock assessment should prioritise sampling over spatial gradients, but repeated monitoring over short time scales is less likely to be warranted if environmental conditions remain stable.  相似文献   

17.
Interpreting global consequences of the Permian-Triassic (P-Tr) extinction requires examination across paleogeographic realms of Pangaea. The Spiti Valley in India, remnant of the peri-Gondwanan shelf, preserved trails of this environmental catastrophe in the Neo-Tethys Ocean. We document new sedimentological observations and high-resolution trace element concentrations and carbon, oxygen, lead isotope data across the P-Tr boundary in Spiti. Framboidal pyrites, fossils and laminated lithology of the Late Permian shales indicate deeper anoxic depositional environment while δ13Corg excursions of 2.4‰ and 3.1‰ in Atargu and Guling outcrops, respectively, identify the P-Tr transition across a clayey, partly gypsiferous ferruginous layer. Sedimentological similarities of this layer to other Neo-Tethyan sections from Transcaucasia and Iran indicate subaqueous oxidation of shallow marine sediments on a regional scale. Light Rare Earth Element – enriched Late Permian shales with conspicuous Ce–Eu anomalies reflect their source from the adjacent Panjal Trap basalts (ca. 289 Ma) of Kashmir. Continental crustal Nb–Ta and Zr–Hf anomalies appear at the P-Tr boundary sediments, and prevail through the overlying Early Triassic carbonates. Original Pb isotope ratios, along with an increasing Pb abundance closer to the P-Tr boundary, distinguish the volcanic source of the Late Permian shales from the continental crustal siliciclastic signature of the Early Triassic carbonates. Our δ13Corg, trace element and Pb isotope record from Spiti indicate catastrophic changes in sediment sources and facies, with effects on carbon cycle and are consistent with an abrupt episode of marine regression and erosional forcing, also observed elsewhere along northern Gondwanaland. Simultaneous eruption of Siberian volcanics and bolide impacts in Parana basin of Brazil and elsewhere implicating impact-triggered volcanism, left catastrophic regional-global imprints on sea level, climate, marine anoxia and tectonic stability that connected the P-Tr crisis across terrestrial and marine realms worlwide.  相似文献   

18.
A close relation of the organic carbon (Corg) content with major has been established for rocks of the Upper Jurassic–Lower Cretaceous Bazhenov Formation. Applying the method of multiple linear regression, it has been demonstrated that the Corgcontent in rocks of the Bazhenov Formation is stringently controlled by its bulk chemical composition. This inference is consistent with the existing ideas regarding a close interrelation between the following main components of rocks: organic carbon and authigenic quartz formed on remains of Radiolaria; pyrite formed in a highly reducing medium of Corg-rich sediments; and terrigenous clayey material diluting the authigenic siliceous–carbonaceous–pyritic matrix. These components chiefly determine the spectrum of major elements in the Bazhenov Formation. The establishment of the close relation between the Corgcontent and the group of major elements refutes the suggestion of some authors that siliceous material was supplied to nonlithified sediments of the Bazhenov sea by hydrothermal solutions, because this mechanism would have inevitably upset geochemical relations between elements in the studied rocks.  相似文献   

19.
Uranium geochemistry has been investigated in three acid lakes located on the Canadian Shield and one circumneutral lake in the Appalachian Region of Eastern Canada. In all Shield lakes, dissolved U concentrations were higher in the porewater than in the overlying water. In one of them, whose hypolimnion is perennially oxic, U released to porewater at depths of Fe remobilization was removed from the porewater at depths of Fe oxyhydroxides precipitation; these similarities in the U and Fe profiles indicate that part of the U becomes associated to Fe oxyhydroxides. The dissolved U and Fe profiles in the other two Shield lakes, whose hypolimnions were anoxic when sampled, did not show any significant recycling of these elements in the vicinity of the sediment-water interface and both elements diffused from the sediment to the overlying water. In contrast, in the Appalachian Lake, dissolved U concentrations were higher in the overlying water than in porewater, strongly decreased at the vicinity of the sediment-water interface and then remained relatively constant with sediment depth. Diagenetic modeling of the porewater U profiles, assuming steady-state, reveals that authigenic U always represented ?3% of the total U concentration in the sediments of all lakes. This observation indicates that diagenetic reactions involving U are not quantitatively important and that most of the U was delivered to the sediments at our study sites as particulate U and not through diffusion across the sediment-water interface, as is seen in continental margin sediments. Comparison of the U:Corg and U:Fe molar ratios in diagenetic material collected across the sediment-water interface with Teflon sheets and in surface sediments (0-0.5 cm) of the lake having a perennially oxic hypolimnion suggest that solid phase U was mainly bound to organic matter originating from the watershed; a strong statistical correlation between sediment non-lithogenic U and Corg in the Appalachian Lake supports this contention. Thermodynamic calculations of saturation states suggest that dissolved U was not removed from porewater through precipitation of UO2(s), U3O7(s) and U3O8(s) as previously proposed in the literature.  相似文献   

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