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1.
Long-term carbon cycling and climate change are strongly dependent on organic carbon (OC) burial in marine sediments. Radiocarbon (14C) has been widely used to constrain the sources, sinks, and processing of sedimentary OC. To elucidate the dominant controls on the radiocarbon content of total organic carbon (14CTOC) accumulating in surface sediments we construct a box model that predicts 14CTOC in the sediment mixed layer (measured as fraction modern, Fm). Our model defines three distinct OC pools (“degradable,” “semi-labile,” and “refractory”) and assumes that 14CTOC flux to sediments is exclusively derived from surface ocean primary productivity, and hence follows a “generic” surface ocean dissolved inorganic carbon (DIC) bomb curve. Model predictions are compared to a set of 75 surface sediment samples, which span a wide geographic range and reflect diverse water column and depositional conditions, and for which sedimentation rate and mixed-layer depth are well characterized. Our model overestimates the Fm value for a majority (65%) of these sites, especially at shallow water depths and for sites characterized by depleted δ13CTOC values. The model is most sensitive to sedimentation rate and mixed-layer depth. Therefore, slight changes to these parameters can lead to a match between modeled and measured Fm values at many sites. Yet, in some cases, we find that measured Fm values cannot be simulated without large and unrealistic changes to sedimentation rate and mixed-layer depth. These results point to sources of pre-aged OC to surface sediments and implicate soil-derived terrestrial OC, reworked marine OC, and/or anthropogenic carbon as important components of the organic matter present in surface sediments. This approach provides a valuable framework within which to explore controls on sedimentary organic matter composition and carbon burial over a range of spatial and temporal scales.  相似文献   

2.
The quantification of carbon burial in lake sediments, and carbon fluxes derived from different origins are crucial to understand modern lacustrine carbon budgets, and to assess the role of lakes in the global carbon cycle. In this study, we estimated carbon burial in the sediment of Lake Qinghai, the largest inland lake in China, and the carbon fluxes derived from different origins. We find that: (1) The organic carbon burial rate in lake sediment is approximately 7.23 g m−2 a−1, which is comparable to rates documented in many large lakes worldwide. We determined that the flux of riverine particulate organic carbon (POC) is approximately 10 times higher than that of dissolved organic carbon (DOC). Organic matter in lake sediments is primarily derived from POC in lake water, of which approximately 80% is of terrestrial origin. (2) The inorganic carbon burial rate in lake sediment is slightly higher than that of organic carbon. The flux of riverine dissolved inorganic carbon (DIC) is approximately 20 times that of DOC, and more than 70% of the riverine DIC is drawn directly and/or indirectly from atmospheric CO2. (3) Both DIC and DOC are concentrated in lake water, suggesting that the lake serves as a sink for both organic and inorganic carbon over long term timescales. (4) Our analysis suggests that the carbon burial rates in Lake Qinghai would be much higher in warmer climatic periods than in cold ones, implying a growing role in the global carbon cycle under a continued global warming scenario.  相似文献   

3.
Rare earth elements in pore waters of marine sediments   总被引：2，自引：0，他引：2  
The rare earth elements (REEs) were measured in pore waters of the upper ∼25 cm of sediment from one site off Peru and three sites on the California margin. The pore water REE concentrations are higher than sea water and show systematic down core variations in both concentration and normalized pattern. From these analyses and from comparison to other chemical species measured (dissolved Fe, Mn, Ba, oxygen, nitrate, phosphate), it is suggested that pore water REEs can be grouped into three categories: those that are from an Fe-source, those that are from a POC-source, and cerium oxide. REEs from the Fe-source appear where anoxia is reached; they have a distinctive “middle-REE (MREE) enriched” pattern. The concentrations in this source are so elevated that they dominate REE trends in the Fe-oxide reduction zone. The net result of flux from the POC-source is relative enrichment of heavy-REEs (HREEs) over light-REEs (LREEs), reflecting remineralizing POC and complexation with DOC. A common “linear” REE pattern, seen in both oxic and anoxic sediments, is associated with this POC-source, as well as a “HREE enriched” pattern that is seen in surficial sediments at the Peru site. Overall, the pore water results indicate that Mn-oxides are not an important carrier of REEs in the oceans.A REE biogeochemical model is presented which attempts to reconcile REE behavior in the water and sediment columns of the oceans. The model proposes that POC, Fe-oxide and Ce-oxide sources can explain the REE concentration profiles and relative abundance patterns in environments ranging from oxic sea water to anoxic pore water. The model is also consistent with our observation that the “Ce-anomaly” of pore water does not exceed unity under any redox condition.  相似文献   

4.
The particulate organic matter in < 63 µm surface sediments from the Mackenzie River and its main tributaries was studied using Rock-Eval pyrolysis and organic petrology. The organic matter in the sediments is dominated by refractory residual organic carbon (RC) of mainly terrigenous nature, as indicated by abundant inertinite, vitrinite, and type III kerogen. Sediments from the tributaries contained significantly more algal-derived organic matter than from the main channel of the river, highlighting the importance of low-energy system dynamics in the tributaries, which allows modest algal production, more accumulation, and better preservation of autochthonous organic matter. This is particularly true for tributaries fed by lacustrine systems, which showed the highest S1 and S2 fractions, and consequently higher total particulate organic carbon (POC) in the basin. Organic petrology of the sediment samples confirms abundant liptinitic materials (i.e., fat-rich structured algae, spores and pollen, cuticles, and resins). Forest fire and coal deposits are also confirmed to contribute to the basin. Assuming that suspended and fine surfacial sediments have a similar OC composition, the Mackenzie River is estimated to deliver a total POC flux of 1.1 Mt C/yr to its delta, of which 85% is residual carbon with liptinitic OC (S1 + S2) and S3 accounting for another 9% and 6%, respectively.  相似文献   

5.
Molybdenum mining in the Knabena—Kvina drainage basin (1918–1973) left more than eight million tons of tailings in two small lakes in the headwater area of the Knabena river. The piles, that reach above the water surface, were freely eroded until a dam was built to reduce the dispersion in 1976. Sampling of tailings and fluvial sediments took place almost 20 years later. Sampling media were natural sediment sources, 1-cm-thick slices of overbank sediments of various depths, material from the tailings pond, sandbars, stream sediments, fjord sediments, and integrated samples of floodplain surfaces (0–25 cm). In total 734 samples were collected. Chemical analysis (ICP-AES after aqua regia or HNO3 extraction) showed that overbank sediments at a certain depth represent the pre-industrial trace metal concentrations within the drainage basin. The tailings and recent fluvial sediments were enriched in approximately the same element suite. The highest enrichment factors were obtained for Cu (8–53) and Mo (22–57). Fluvial processes in the tailings pond have probably selectively eroded fine-grained, low-density particles. Thus, coarse chalcopyrite may have been left behind, while molybdate associated with fine-grained particles may have been selectively entrained causing dilution of Cu and enrichment of Mo in the downstream fluvial sediments. In the sandbars, the highest Cu and Mo concentrations were found in fine-grained sediments downstream of a low-gradient reach that act as a bedload trap. On the floodplains, it is seen that the first areas to be inundated in a flood situation (proximal to the river and in depressions) have the highest metal concentrations. For regional geochemical mapping it is suggested that overbank sediment profiles along river reaches with a laterally stable or slowly migrating channel, should be sampled. In such floodplains, pre-industrial overbank sediments are usually preserved at depth. In case of laterally unstable reaches upstream of the sampling point, polluted and unpolluted sediments may be interlayered or mixed. Therefore, samples should be collected from various depths or sedimentary units in such profiles. A similar sampling strategy should probably be adopted to detect vertical migration of elements especially in areas with acid rain and low bedrock buffer capacity. To obtain high contrasts between polluted and unpolluted drainage basins, the overbank sediment profiles should be within the proximal part of the floodplain.  相似文献   

6.
Lake Kivu is a gas-charged East African rift lake with currently anoxic bottom water. The extractable compounds and residual organic matter of a short sediment core have δ13C values typical of lacustrine microbial detritus. The total extracts consist primarily of polar compounds such as n-alkanoic acids, hydroxyalkanoic acids, triterpenoids, steroids and monosaccharides, with minor amounts of n-alkanes and n-alkanols. These tracer compounds and δ13C values indicate that the organic matter in the surficial and deeper sedimentary record was dominated by bacterial sources. The sapropelic sediment between these horizons contains organic matter from primarily algal with lesser bacterial input. Terrestrial organic markers are minor in all samples. The major fractions of the compounds in the total extracts were oxidized in the upper water column prior to transit through the anoxic bottom water to sedimentary deposition. The sapropelic horizon may reflect lake water turnover with ventilation or hydrothermal activity and consequently increased algal blooms.  相似文献   

7.
Fluxes of particulate organic carbon (POC) through the oxygen deficient waters in the eastern tropical North Pacific were found to be relatively less attenuated with depth than elsewhere in the eastern North Pacific. The attenuation coefficient (b) for the flux was found to be 0.40 versus the composite value of 0.86 determined by Martin et al. (1987). To examine this further, sinking POC was collected using sediment traps and allowed to degrade in oxic and suboxic experiments. Using a kinetic model, it was found that degradation proceeded at similar rates (roughly 0.8 day−1) under oxic and suboxic conditions, but a greater fraction of bulk POC was resistant to degradation in the suboxic experiments (61% vs. 23%). Amino acids accounted for 37% of POC collected at 75m, but following degradation the value dropped to 17% and 16% in the oxic and suboxic experiments respectively. POC collected from 500m was 10% amino acids. The non-AA component of POC collected at 75m was not degraded under suboxic conditions, while under oxic conditions it was. These results suggest that microbes degrading OC under suboxic conditions via denitrification preferentially utilize nitrogen-rich amino acids. This preferential degradation of amino acids suggests that 9% more nitrogen may be lost via water column denitrification than is accounted for when a more “Redfieldian” stoichiometry for POC is assumed.  相似文献   

8.
Studies of lake sediments on Sejerø in southern Kattegat indicate a treeless arctic environment with the dwarf shrub Salix polaris, herbs and wetland mosses. The mean July temperature was around 8 to 10°C. An AMS radiocarbon age determination of a Salix twig yielded an age of around 36 000 14C yr BP, which is in accordance with previous conventional dating of bulk sediment samples. Copyright © 2006 John Wiley & Sons, Ltd.  相似文献   

9.
Burial of organic carbon (OC) in ocean sediments acts as the ultimate long-term sink for both terrestrial and marine carbon, however, the mechanisms controlling the preservation of this carbon are poorly understood. To better understand these mechanisms, we applied solid-state 13C nuclear magnetic resonance (NMR) spectroscopy, along with elemental, stable carbon isotopic (δ13C) and lignin phenol analyses, to size and density fractions of sediments influenced by either mixed terrestrial and marine OC inputs (Washington Coast slope) or dominantly marine inputs (Mexican Margin). Elemental, isotopic and lignin analyses all reveal that within the Washington Coast sediment, the OC mixes linearly between nitrogen-poor and 13C-depleted, lignin-rich OC in the large and light fractions and nitrogen-rich and 13C-enriched, lignin-poor OC in the small and dense fractions, suggesting that this sediment contains a two-component mixture of terrestrial vascular plant- and marine-derived OC. The integral areas of each of seven NMR spectral regions in the different samples trend linearly when plotted versus δ13C signature, with most R2 values of 0.78 or greater, demonstrating that the NMR spectra of the two sources of carbon also mix linearly between the two endmembers. The terrestrial endmember in this sediment appears to be dominated by lignin and black carbon whereas the source of the marine endmember is less clear from the NMR spectra. In contrast, all of the analyses indicate that OC in the Mexican Margin sediment fractions is homogenous and derives almost exclusively from marine sources. It appears that selective preservation of (bio)chemically recalcitrant lignin and black carbon is the primary mechanism of preservation of terrestrial OC, whereas mineral-protection is the dominant mechanism preserving marine OC in the Washington coast sediment. There is little evidence showing that either preservation mechanism functions in the Mexican Margin sediments.  相似文献   

10.
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11.
Sediments in Lake Qinghai archive important information about past environmental changes. In order to faithfully interpret the sediment records and constrain the elemental cycles, it is critical to trace various sources of sediments in the lake. The results show that the elemental input–output budgets are imbalanced for most major elements between riverine fluxes and mass accumulation rate (MAR) of Lake Qinghai sediments. A realistic model must include contributions of dry/wet atmospheric deposition that allow the major element mass balance for the lake to be defined. The budget estimation is based on mass balances of Si and Al, which are relatively immobile and carried to the lake via particulate forms. Estimated annual budget of dry atmospheric deposition is ∼1.3 ± 0.3 × 103 kt/a (accounting for ∼65% of the total inputs) to the lake sediments, assuming local loess within the catchment as a candidate for dry atmospheric deposition to the lake. The resultant flux of 300 ± 45 g/m2/a falls within the flux average of the desert area (400 g/m2/a) and the loess plateau (250 g/m2/a), consistent with the geographical setting of Lake Qinghai. The role of atmospheric deposition would be more significant if wet deposition via rainfall and snow were taken into account. This highlights the potential importance of dust as a significant source for sediment preservation flux for other catchments worldwide. The results also indicate that nearly all Ca input was preserved in the lake sediments under modern conditions, consistent with Ca2+ supersaturation of the lake water.  相似文献   

12.
A geochemical investigation was carried out mainly in a 14-km thick sedimentary sequence of late Precambrian age. The project included analysis of rock samples and drainage samples for Cu, Co, and Zn. The drainage samples were heavy-mineral concentrates and stream sediment samples.The results for the drainage sediments distinguish three well defined cupriferous horizons in the sedimentary column. Lithogeochemical studies of quartzites, pelites, and carbonates confirm that the anomalous values obtained in the drainage sediments arise from several Cu-mineralized horizons.The study has shown that geochemical prospecting appears to be well suited to Cu prospecting in Central East Greenland under arctic climate conditions even with a low sampling density of one sample per 5–10 km2 for the drainage samples, and one sample per 10–100 m of the sedimentary stratigraphic column for the rock samples.  相似文献   

13.
Esters of phytol or related isoprenoid acids and fatty acid esters of pentacyclic triterpenoid alcohols and sterols have been isolated from lacustrine sediments varying in age from contemporary to c. 50,000 years old. The esters were analysed by C-GC-MS and identified by GC retention data and mass spectral interpretation based on comparison with authentic compounds.In surface sediment of a productive lake, phytyl and steryl esters are biochemical markers of input from algal and Zooplankton sources. Esters of pentacyclic triterpenols detected in an older, peat-derived sediment may reflect constituents of peat-forming plant species. In sediments derived mainly from terrestrial organic matter, steryl esters containing the same acyl group showed a lower stanol/Δ5-stenol ratio than did the corresponding free sterols.  相似文献   

14.
The burial characteristics and toxicity risks associated with n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in the riverine and estuarine sediments of the Daliao River watershed were investigated based on three sediment cores. The sum of the n-alkane and PAH concentrations, normalized to organic carbon (OC), ranged from 0.27 to 63.09 μg g?1OC?1 and 6.60 to 366.20 μg g?1OC?1, respectively. The features and the history of industrial activities, such as the oil and chemical industries and port activities near the river and estuary, resulted in different distributions and sources of hydrocarbons. The sources of pollution were identified based on n-alkane indexes and on diagnostic ratios of PAHs. The diagnostic ratios indicated that the n-alkanes were derived from both biogenic and petrogenic sources in different proportions and that the PAHs were derived primarily from petrogenic combustion sources. A hierarchical cluster analysis grouped the core samples into two clusters. The first cluster, river sediments, corresponded to industrial activities; the second cluster, estuarine sediments, corresponded to port shipping activities. The toxic potency of the PAHs in the cores was assessed in terms of toxic equivalents (TEQs) of dibenzo[a,h]anthracene and benzo[a]pyrene. The top layer of the sediment in the cores had a relatively high toxicity. The TEQ values for benzo(a)pyrene (TEQBaP) and dioxins (TEQTCDD) furnished a consistent assessment of the PAHs in the sediment cores.  相似文献   

15.
This study reports a multi-parameter geochemical investigation in water and sediments of a shallow hyper-eutrophic urban freshwater coastal lake, Zeekoevlei, in South Africa. Zeekoevlei receives a greater fraction of dissolved major and trace elements from natural sources (e.g., chemical weathering and sea salt). Fertilizers, agricultural wastes, raw sewage effluents and road runoff in contrast, constitute the predominant anthropogenic sources, which supply As, Cd, Cu, Pb and Zn in this lake. The overall low dissolved metal load results from negligible industrial pollution, high pH and elevated metal uptake by phytoplankton. However, the surface sediments are highly polluted with Pb, Cd and Zn. Wind-induced sediment resuspension results in increased particulate and dissolved element concentrations in bottom waters. Low C/N ratio (10) indicates primarily an algal source for the sedimentary organic matter. Variation in sedimentary organic C content with depth indicates a change in primary productivity in response to historical events (e.g., seepage from wastewater treatment plant, dredging and urbanization). Primary productivity controls the enrichment of most of the metals in sediments, and elevated productivity with higher accumulation of planktonic debris (and siltation) results in increased element concentration in surface and deeper sediments. Aluminium, Fe and/or Mn oxy-hydroxides, clay minerals and calcareous sediments also play an important role in adsorbing metals in Zeekoevlei sediments.  相似文献   

16.
The grain size of the loess‐like sediment in the Jinsha River Valley is essentially similar to that of typical loess, and it differs from that of the fluvial sediment in the Jinsha River area. We conclude that the loess‐like sediment is of aeolian origin, as is the loess of the Chinese Loess Plateau. The geochemical characteristics of the loess‐like sediment are similar to those of dammed lake and fluvial sediments in the same area, which is significantly different from those of the typical loess in NW China. The geochemical characteristics show that the loess‐like sediment originated from proximal materials. Combined with the grain‐size distribution pattern of the aeolian deposits, we suggest that the loess‐like sediment of the Jinsha River Valley originated from the dammed lake and fluvial sediments that accumulated in the valley. The local mountain‐valley wind circulation (especially the valley wind in winter and spring) provided the transport force for the loess‐like sediment. The presentation of the loess‐like sediment may indicate the appearance of the grassland and forest steppe and the beginning of the dry‐hot valley phenomenon.  相似文献   

17.
We present a mineralogical and geochemical study of core MD012404, retrieved from the central Okinawa Trough (OT) of the East China Sea. Our studies reveal that the sediment sources of the core have been changed through time during the past 100 ka. Our mineralogical proxies indicate that the sediments source from the Yangtze River correlates well sea-level changes before 24 ka. Our Ti/Al ratios otherwise indicate an increase of sediment supply from eastern Taiwan after 26 ka. The cooler climate of the Last Glacial Maximum (LGM, 23～19 ka) led to a reduction in fluvial sediments from the Yangtze River. However, subsequent climate warming (after ～19 ka) resulted in an abrupt increase in fluvial sediments. After the LGM, the Kuroshio intrusion flow into the OT may have increased. We also infer anomalous changes in eolian sources transported by winter monsoons during the LGM and at 80 ka based on an eolian mineralogical indicator (feldspar). We conclude that the sediment source of core MD012404 is primarily of terrestrial origins, but influenced by sea-level changes and variations in the East Asian monsoon.  相似文献   

18.
Seismostratigraphical studies of the 11.8‐km2‐large and ~140‐m‐deep Lake Bolshoye Shchuchye, Polar Ural Mountains, reveal up to 160‐m‐thick acoustically laminated sediments in the lake basin. Using a dense grid of seismic lines, the spatial and temporal distributions of the sedimentary history have been reconstructed. Three regional seismic horizons have been identified and correlated with the well‐dated 24‐m‐long sediment core retrieved from the lake. Isopach maps constructed from the seismic data show four phases of sedimentation. A contour map of the deepest regional seismic reflector represents the earliest hemipelagic sedimentation in the lake. Three contour maps represent time intervals covering the last 23 cal. ka based on the well‐dated core stratigraphy from the lake. The detailed time constraints on the upper stratigraphical units in the lake allow calculation of the lake's development in terms of sediment fluxes and the denudation rates from the Last Glacial Maximum (LGM) to the present. The sedimentation in Lake Bolshoye Shchuchye has been dominated by hemipelagic processes during at least the last 24 cal. ka BP only locally interrupted by delta progradation and slope processes. A major shift in the sediment accumulation at c. 18.7 cal. ka BP is interpreted to mark the end of the local glacial maximum, greatly reduced denudation and the onset of the deglaciation period; this also demonstrates how fast the glaciers melted and possibly disappeared at the end of the LGM. The denudation rate during the Holocene is only a fifth of the LGM rate. The age of the oldest stratified sediments in Lake Bolshoye Shchuchye is not well constrained, but estimated as c. 50–60 ka.  相似文献   

19.
To examine the biogeochemistry of amino acids (AAs) in the sediment of Lake Taihu, surface sediments (0–3 cm) and deeper sediments (18–21 cm) were collected at 21 sites from different ecotype zones of the lake. AAs were extracted from the sediments, and the total hydrolyzable amino acids (THAA) were determined by high-performance liquid chromatography instrument. The THAA contents in Taihu sediment were much lower than that in marine sediments, ranging from 6.84 to 38.24 μmol g−1 in surface sediments and from 2.91 to 18.75 μmol g−1 in deeper sediments in Taihu, respectively. AAs were a major fraction of the organic matter (OM) and organic nitrogen in Taihu sediments. The AAs on average contributed 8.2% of organic carbon (OC) and 25.0% of total nitrogen (TN) from surface sediments, and 5.9% of OC and 20.5% of TN in deeper sediments, respectively. AA composition provided very useful information about the degradation of OM. Glycine (Gly) and lysine (Lys) were the predominant forms of AAs in the sediments, irrespective of lake regions, followed by alanine, glutamic acid, serine (Ser), and aspartic acid (Asp). The high concentrations of Gly, Lys, and Ser suggested that these forms of AAs were relatively refractory during OM degradation in sediments. The relationship between the Asp/Gly ratio and Ser + Thr [mol%] indicated that OM in surface sediment was relatively fresher than that in deeper sediments. The AAs-based degradation index (DI) gave a similar conclusion. The composition and DI of AAs in surface sediments are markedly different across different zones in Taihu. The percentages of AAs to organic carbon (AA-C%) and total nitrogen (AA-N%) were higher in phytoplankton-dominated zones than those in macrophyte-dominated zones. These results suggest that DI could provide useful information about the degradation of OM in shallow lakes such as Taihu.  相似文献   

20.
Assessments of carbonate platform reef–lagoon sediments and benthic habitats around Rodrigues Island (south-west Indian Ocean) have been undertaken in order to examine carbonate sediment textural properties and the controls on texturally-defined sediment fabrics. Reef–lagoon sediments, sampled from across the expansive (~ 8 km wide) carbonate-dominated windward platform, principally comprise poorly sorted medium- to coarse-grained bioclastic sands, composed of a low diversity of grain constituents — predominantly non-geniculate coralline algal bioclasts. Despite a marked homogeneity in sediment compositional and grain size properties, eight distinct sediment textural groups can be identified that form a heterogeneous mosaic across the contemporary reef–lagoon system. Only along the narrow outer platform margins (reef crest, sand apron and outermost lagoon environments) do we observe consistent (predictable) transitions in sediment textural groups, where physical processes are the primary drivers of selective sediment transport and sorting. In contrast, across the main expanse of the lagoon, the sediment substrates are characterised by an irregular mosaic of texturally-defined sediment groups — formed primarily as a function of sediment bio-retexturing. The burrowing activities of alpheid and callianassid shrimps are particularly important in this respect and impart a distinctly unique textural fabric to the upper sediment horizons in the environments in which the respective organisms occur. The consequence of this is that, at the platform system scale, individual, texturally-defined sediment groups are relatively poor indicators of prevailing hydrodynamic regimes or of local sediment production, reflecting more the biological action of organisms inhabiting the substrate. This has important implications for understanding the development of carbonate sediment fabrics in the context of palaeoenvironmental reconstructions and for interpreting a key diagnostic criteria of carbonate microfacies.  相似文献   

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