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1.
Between 1990 and 2007, twenty-nine box cores were recovered within the Arctic Ocean spanning shelf, slope and basin locations, and analyzed for aluminum (Al), manganese (Mn), other inorganic components and organic carbon (COrg). Using these core data together with literature values, we have constructed budgets for Al and Mn in the Arctic Ocean. Most of the Al and Mn entering the Arctic comes from rivers or coastal erosion, and almost all of these two elements is trapped within the Arctic. Total Mn distributions in sediments reflect the recycling and loss of much of the Mn from shelf sediments with ultimate burial over the slopes and in basins. Mn enrichments observed as bands in long cores from the basins appear to co-occur with inter-glacial periods. Our Mn budget suggests that change in sea level associated with the accumulation and melting of glaciers is a likely cause for the banding. The Arctic Ocean, which presently contains as much as 50% shelf area, loses most of that when global sea level falls by?~120?m during glacial maxima. With lower sea level, Mn input from rivers and coastal erosion declines, and inputs become stored in permafrost on the sub-aerial shelves or at the shelf margin. Sea-level rise re-establishes coastal erosion and large riverine inputs at the margin and initiates the remobilization of Mn stored on shelves by turning on algal productivity, which provides the COrg required to reduce sedimentary Mn oxyhydroxides.  相似文献   

2.
Freshwater chlorophycean algae are characteristic organic-walled microfossils in recent coastal and shelf sediments from the Beaufort, Laptev and Kara seas (Arctic Ocean). The persistent occurrence of the chlorophycean algae Pediastrum spp. and Botryococcus cf. braunii in marine palynomorph assemblages is related to the discharge of freshwater and suspended matter from the large Siberian and North American rivers into the Arctic shelf seas. The distribution patterns of these algae in the marine environments reflect the predominant deposition of riverine sediments and organic matter along the salinity gradient from the outer estuaries and prodeltas to the shelf break. Sedimentary processes overprint the primary distribution of these algae. Resuspension of sediments by waves and bottom currents may transport sediments in the bottom nepheloid layer along the submarine channels to the shelf break. Bottom sediments and microfossils may be incorporated into sea ice during freeze-up in autumn and winter leading to an export from the shelves into the deep sea. The presence of these freshwater algae in sea-ice and bottom sediments in the central Arctic Ocean confirm that transport in sea ice is an important process which leads to a redistribution of shallow water microfossils.  相似文献   

3.
Increased offshore development in the Alaskan Arctic has stimulated interest in assessing potential impacts to the environment before the onset of any adverse effects. Concentrations of trace metals in sediments are used in this paper to provide one sensitive indicator of anthropogenic inputs from offshore activity over the past several decades. Sediments in coastal waters of the western Beaufort Sea are patchy with respect to sediment granulometry, organic carbon content, and concentrations of trace metals. However, results for surface sediments and age-dated cores show that nearly all samples contain natural concentrations of Ag, Ba, Be, Co, Cr, Cu, Hg, Ni, Pb, Sb, Tl, V and Zn, with metal/Al ratios that have been constant for many decades. Metal concentrations for incoming river-suspended matter compare well with sediment metal values and, along with vertical distributions in sediments, show no discernible diagenetic impacts that distort the sedimentary record for metals, except for Mn, As and possibly Cd. Slightly elevated concentrations of Ba, Hg, Ag, Sb and Zn were observed in a total of eight instances or in only 0.7% of the 1,222 data points for metals in surface sediments.  相似文献   

4.
利用电感耦合等离子体质谱仪测定了中国南极科考21~27航次期间获取的普里兹湾表层沉积物中Cu、Pb、Zn、Cd、Cr、Co、Al、Fe、Mn的含量,分析了普里兹湾微量元素的分布特征,结合沉积物粒度分布、生物硅含量,并利用富集系数和主成分分析的方法,探讨了微量元素的物源指示意义。研究结果表明:普里兹湾沉积物中的微量元素含量与南大洋其他海域具有很好的可比性。Cu、Zn、Cr、Co、Fe、Mn含量在陆坡深海区明显高于冰架边缘区和陆架区;Al、Pb含量在冰架边缘区较高;而Cd含量在陆架区相对较高。人类活动对普里兹湾沉积物中的微量元素没有明显的影响,南极大陆岩石风化产物和海洋生物源性沉降是其主要来源。冰架边缘区及陆架破折处P2-9站位的微量元素主要为岩源性输入。陆架区、陆坡深海区的微量元素Cu、Zn、Cr、Co、Fe、Mn明显受到生源性物质输入的影响。而普里兹湾沉积物中Cd则主要来源于硅藻的吸收利用及硅质软泥的富集。  相似文献   

5.
Clay-mineral, heavy-mineral, and elemental distributions in sediments from the Arctic Ocean and the adjacent Laptev and Kara seas can be attributed to the geology of the hinterland and the transport of terrigenous material by rivers onto the shelves. Kara Sea sediments are characterized by increased contents of smectite and elevated Ni/Al-, Ti/Al-, and Cr/Al ratios. In the western Laptev Sea sediments are enriched in smectite and clinopyroxene and increased in Ti/Al-, Cr/Al-, and Ca/Al ratios. The composition of the sediments reflects suspended matter input from the large trap basalt of the Putoran Mountains. The eastern Laptev Sea sediments display increased illite and amphibole contents as well as a chemical composition similar to average shale. This composition is due to the discharge from the Lena and Yana rivers, which drain a large catchment area consisting of sedimentary Mesozoic and Paleozoic rocks. Material from the eastern Laptev Sea is transported by ocean currents and sediment-laden sea ice along the Transpolar Drift into the central Arctic Ocean. This is indicated by similar values of Ti/Al-, Cr/Al-, Rb/Al-, and K/Al ratios as well as increased concentrations of amphibole and illite, determined in sediments from the Lomonosov Ridge. A minor input from the Beaufort Sea into the central Arctic Ocean is suggested from increased Ca/Al ratios and increased contents of opaque minerals.  相似文献   

6.
Bulk chemical, mineralogical and selective leach analyses have been made on a suite of abyssal ferromanganese nodules and associated sediments from the S.W. equatorial Pacific Ocean. Compositional relations between nodules, sediment oxyhydroxides and nearby ferromanganese encrustations are drawn assuming that the crusts represent purely hydrogenetic ferromanganese material. Crusts, δMnO2-rich nodules and sediment oxyhydroxides are compositionally similar and distinct from diagenetic todorokitebearing nodules. Compared to Fe-Mn crusts, sediment oxyhydroxides are however slightly enriched, relative to Mn and Ni, in Fe, Cu, Zn, Ti and Al, and depleted in Co and Pb, reflecting processes of non-hydrogenous element supply and diagenesis. δMnO2 nodules exhibit compositions intermediate between Fe-Mn crusts and sediment oxyhydroxides and thus are considered to accrete oxides from both the water column and associated sediments.Deep ocean vertical element fluxes associated with large organic aggregates, biogenic calcite, silica and soft parts have been calculated for the study area. Fluxes associated with organic aggregates are one to three orders of magnitude greater than those associated with the other phases considered, are in good agreement with element accumulation rates in sediments, and are up to four orders of magnitude greater than element accumulation rates in nodules. Metal release from labile biogenic material in surface sediments can qualitatively explain the differences between the composition of Fe-Mn crusts and sediment oxyhydroxides.Todorokite-rich diagenetic nodules are confined to an eastwards widening equatorial wedge. It is proposed that todorokite precipitates directly from interstitial waters. Since the transition metal chemistry of interstitial waters is controlled dominantly by reactions involving the breakdown of organic carbon, the supply and degradation rate of organic material is a critical factor in the formation of diagenetic nodules. The wide range of (trace metal/Mn) ratios observed in marine todorokite reflects a balance between the release of trace metals from labile biogenic phases and the reductive remobilisation of Mn oxide, both of which are related to the breakdown of organic carbon.  相似文献   

7.
通过对中国第3次和第4次北极考察在白令海和西北冰洋采集的65个表层样沉积物中生物标记物四醚膜类脂物(GDGTs)的研究,发现西北冰洋表层沉积物中类异戊二烯和支链GDGTs的浓度分布大致以楚科奇海和波弗特海的陆坡为界线,呈现南高北低的特征,这一特征主要与水体生产力和陆源有机质的输入量有关.基于GDGTs的陆源输入指数BIT显示,从楚科奇海北部到高纬度区的阿尔法脊,陆源有机质的相对比例明显增加,与有机碳稳定同位素等结果一致,表明BIT可以用来指示北极陆源有机质输入量的变化.应用前人TEXL86-SST方程估算的研究区表面海水温度SST与现代年均SST和夏季平均SST的相关性较差,原因可能与陆源输入的类异戊二烯GDGTs干扰以及低的古菌生产力有关.从季节性海冰覆盖区到永久性海冰覆盖区,基于支链GDGTs的环化指数CBT明显升高,可能反映了CBT对海冰覆盖状况的响应,但其响应机制还不清楚.基于支链GDGTs的环化指数CBT和甲基化指数MBT估算的北极陆地年均大气温度和土壤pH差异较大,可能是由表层沉积物的来源复杂以及混合作用造成的.  相似文献   

8.
Surficial sediment samples were collected at 47 stations in Little Traverse Bay, Lake Michigan, to determine the geochemical associations between certain rare earth elements (REE's) and trace metals. Each sample was analyzed for carbonate carbon, organic carbon, grain size, and the elements Al, Ca, Ce, Co, Cr, Eu, Fe, Hf, La, and Mn. Two distinct Ce subpopulatins were identified by graphical analysis, and an R-mode factor analysis was applied to data from the “enriched” Ce subpopulation (18 samples). Results show that the REE's and trace metals are primarily enriched in the authigenic phase of these sediments. Partial correlation analyses indicate that the REE's are primarily associated with hydrous Fe oxides relative to organic matter in this phase. The ratio of Ce/La concentrations increased markedly from the bay margins to the central trough of the bay, indicating that Ce, similar to Fe, exhibits a variable oxidation state in the authigenic phase of nearshore fine-grained sediments. The results of the present study suggest that the REE's and trace metals behave coherently in the authigenic phase of recent lacustrine sediments, and the REE's may be useful as geochemical tracers to differentiate between trace metal enrichments in surface sediments as a result of diagenesis and pollution loadings.  相似文献   

9.
Following a catastrophic flash flood in July 1996, as much as 50 cm of post-glacial clays were deposited in less than 2 days in the upper reaches of the Saguenay Fjord (Quebec, Canada), disrupting the normal sedimentation and diagenetic regimes. We report detailed geochemical analyses of sediments (porosity, Eh, organic and inorganic carbon, Fe and Mn reactive solid phases, and acid volatile sulfide) and porewaters (salinity, dissolved organic carbon (DOC), Fe(II), Mn(II), nitrate, ammonium, and sulfate) for seven stations located in the Saguenay Fjord. Three of these (SAG-05, SAG-09, and SAG-30) were visited in 1996 and once per year thereafter to document the chemical evolution of the sediment toward a new steady state. The flood deposits contain less organic carbon and more inorganic carbon than the indigenous fjord sediments. The flood deposit modified the distribution patterns of reactive Mn and Fe as a result of the reduction of Mn and Fe oxides delivered with the deposit and those concentrated at the now buried former sediment-water interface. Most of the Mn(II) migrated to the new sediment-water interface, where a Mn-rich layer was formed. In contrast, much of the Fe(II) was precipitated as sulfides and remained trapped at or close to the old interface. A nitrate peak developed in the porewater at the old sediment-water interface, possibly because of the oxidation of ammonia by Mn oxides. The distributions of porewater DOC within the flood deposit correlate with the distributions of dissolved Mn(II) and Fe(II), suggesting that adsorbed DOC was released when metal oxides were reduced.  相似文献   

10.
In the present study, the geochemistry of 49 surficial-bed and 101 core sediment samples is investigated to clarify the origin of trace metals in the Cua Luc Estuary and Ha Long Bay, which is a famous World Natural Heritage Site in Vietnam. Moreover, the potential mobility of trace metals is also assessed and their relationship with reference elements (Al, Fe, and Ca) and organic matter is established in order to make recommendations for sediment management and monitor future pollution. Generally, trace metals display higher concentrations in Ha Long Bay compared to the Cua Luc Estuary. However, this is controlled by the distribution of the fine (clay?+?silt) fraction, and hence the concentrations of Al, Fe, Ca, and organic matter (OM). The comparison of concentrations of trace metals (normalized towards Al) between the surficial sediments and the subsurface core sediments based on 137Cs datings indicates that almost all surficial-sediment data fall inside or deviate slightly from the 95 % prediction interval of a background regression line. In addition, as determined by a Community Bureau of Reference three-step extraction, trace metals mainly dominate in the residual fraction (assumed to relate to crystal lattice of primary and secondary minerals), and this fraction does not change much in recent sediment layers. Therefore, trace metals are supposed to be derived from natural bio/geochemical processes and are characterized by a low potential mobility. Consequently, the established linear regression relationships of trace metal vs. Al or multiple regression relationships of trace metal vs. multi-elements (Al, Fe, Ca, and OM) are useful for the prediction of background levels of trace metals in sediments in future pollution monitoring and assessment programs.  相似文献   

11.
Trace metals (Mn, Fe, Mo, U, Cr, V) were studied in pore waters of an intertidal flat located in the German Wadden Sea. The study system is an example of a permeable tidal flat system where pore water exchange is affected by tidal driven pressure gradients besides diffusion. Permanently installed in situ samplers were used to extract pore waters down to 5 m depth throughout one year. The samplers were either located close to the tidal flat margin or in central parts of the tidal flat. Despite dynamic sedimentological and hydrological conditions, the general trends with depth in deep tidal flat pore waters are remarkably similar to those observed in deep sea environments. Rates of trace metal cycling must be comparably large in order to maintain the observed pore water profiles. Trace metals further show similar general trends with depth close to the margin and in central parts of the tidal flat. Seasonal sampling revealed that V and Cr vary concurrent with seasonal changes in dissolved organic carbon (DOC) concentration. This effect is most notable close to the tidal flat margin where sulphate, DOC, and nutrients vary with season down to some metres depth. Seasonal variations of Mn, Fe, Mo, and U are by contrast limited to the upper decimetres of the sediment. Their seasonal patterns depend on organic matter supply, redox stratification, and particulate matter deposited on sediment surfaces. Pore water sampling within one tidal cycle provides evidence for pore water advection in margin sediments. During low tide pore water flow towards the creekbank is generated by a hydraulic gradient suggesting that deep pore waters may be seeping out of creekbank sediments. Owing to the enrichment of specific elements like Mn in pore water compared to sea water, seeping pore waters may have an impact on the chemistry of the open water column. Mass balance calculations reveal that the impact of deep pore waters on the Mn budget in the open water column is below 4%. Mn deep pore water discharge of the whole Wadden Sea is estimated to be about 9% of the total dissolved riverine Mn input into the Southern North Sea.  相似文献   

12.
Geochemical analyses of lakebed and core sediments from Lake Sambe on the outskirts of Oda City in Shimane prefecture in southwestern Japan were carried out in order to assess the water quality and the concentration and distribution patterns of sixteen elements. The lake water showed a stratified condition with respect to dissolved O2, and As, Fe, and Mn concentrations in the bottom layers which increased in the summer. The chemical composition of the sediments, as measured by X-ray fluorescence, included major and trace elements (P, Ca, Sc, Ti, V, Cr, Fe, Ni, Cu, Zn, As, Sr, Zr, Pb, and Th), and total sulfur (TS). Elevated values of As, Zn, V, Fe, P, and TS were present in several layers of the upper cores (from 0 to 5 cm) and other surface sediments. Increases in the abundances of these metals in lake sediments are probably related to the reducing condition of the sediments, fine-grained organic rich sediments, and post-depositional diagenetic remobilization. Moreover, correlations between the concentrations of trace metals and iron in the sediments suggest their adsorption onto Fe (oxy)hydroxides, whereas correlations with sulfur indicate that they were precipitated as Fe-sulfides. The average abundances of As, Pb, Zn, and Cu exceeded the lowest effect level and Interim Sediment Quality Guideline values that the New York State Department of Environmental Conservation and the Canadian Council of Ministers of the Environment determined to have moderate impact on aquatic organisms. In addition, concentrations of As and Zn exceeded the Coastal Ocean Sediment Database threshold value, indicating potentially toxic levels. Therefore, the presence of trace metals in the lake sediments may result in adverse effects on biota health.  相似文献   

13.
This paper addresses the problem of relationships between the chemical composition and color of Quaternary marine sediments using the data of X-ray fluorescence analysis for the region of the Mendeleev Rise (Arctic Ocean). The contributions of sedimentation and diagenetic factors to color formation were estimated. It was shown that lithostratigraphic correlations should be performed (with certain limitations) using only sediment layers of dark brown and pink color.  相似文献   

14.
This study was designed to establish the distributions of trace metals (Cd, Co, Cu, Ni, Pb, and Zn), dissolved organic carbon (DOC), and inorganic nutrients (PO4 and H4SiO4) in the water column of the small, relatively pristine Peconic River estuary. We were also able to examine the effects of a harmful microalgal bloom, known as the brown tide, which occurred in the area during our study. Because river inflow to the Peconic estuary is restricted by a small dam at the head of the estuary, direct evaluation of the relative importance of riverine inputs on estuarine metal distributions was possible. The simultaneous analyses of geochemical carrier metals (Al, Fe, and Mn), an indicator of sewage (Ag), and other ancillary parameters (e.g., suspended particulate matter, dissolved O2, chlorophylla) were used to describe the major processes controlling metal concentrations in the dissolved phase. The trace metal distributions indicated two distinct biogeochemical regimes within the estuary: an anthropogenically perturbed region with high metal levels (e.g., Ag, 165 pM; Cu, 51 nM; Zn, 57 nM) at the head (Flanders Bay), and a larger outer region with relatively low metal concentrations. The very similar distributions of some metals (e.g., Mn, Ni) in the Peconic estuary compared to those in estuaries having much higher river flow demonstrated the dominant role of internal processes (e.g., diagenetic remobilization) in controlling these metal patterns. An inverse relationship between dissolved Fe and DOC with cell counts of the brown tide microalgaeAureococcus anophagefferens in our field study suggested a close association with the bloom, although a similar relationship was observed between dissolved Al and brown tide cell counts, implying that removal of Fe could be due to particle scavenging rather than biological uptake.  相似文献   

15.
Major (Al and Fe), minor (Mn) andtrace (As, Cd, Co, Cr, Cu, Hg, Li, Mo, Ni, Pb, Sb, Vand Zn) metals along with material of grain size<63 m, TOC and TN have been determined insediment grab and core samples from the Kara Sea, andthe Ob and Yenisey estuaries, Russia. Surprisingly,the levels of trace metals, with the exception of As,were much lower than was anticipated from speculativereports of extensive contamination in the Arcticmarine areas adjacent to the Siberian coastline ofRussia. Lithium normalization indicates that theabundance and distribution of the metals, with theexception of As and Mo, are controlled by theaccumulation of their fine grained aluminosilicatehost minerals at sites determined by hydrodynamicconditions in the Kara Sea and in the estuaries. Metallevels in the Kara Sea and the Ob and Yeniseyestuaries, except for some anomalous As, Cu and Nivalues, are close to natural baseline levels of otherEurasian Arctic shelf sediments. High levels of As,however, occur in surface and subsurface sediments.The accumulation of As, as well as Mo, can beattributed to the post-depositional diagenetic effectsof Fe-Mn cycling both at and near the sediment waterinterface. Subsurface As and Fe maxima and minimasuggest alternating oxic and anoxic water conditionsduring post-glacial rises in sea level. In contrast tothe results from the adjacent Pechora Sea, in the KaraSea there is no correlation between the levels of Asand radionuclides in the sediments.  相似文献   

16.
A stratigraphic profile of solid phase As was measured to investigate the diagenetic cycling of arsenic and related elements in fluvial sediments of the Meghna River delta plain. The distributions of Fe, Mn, and Al are typically characterized by surficial solid phase enrichment, and As is distributed down to 36.6 m showing similar alternate layers of maxima and minima with Fe, Mn and TOC, which reflects the diagenetic remobilization and periodical differences in source materials of As. Lithological characteristics and geochemical data suggest that elevated levels of As are found in organic-matter-rich clay and silty sand rather than sand samples, with occasionally enriched As content in iron-oxyhydroxide-coated sand grains. Arsenic demonstrates a positive and significant co-variation with total organic carbon in sediments, which suggests the important role of particulate and colloidal organic matter and biological activity in controlling the distribution of arsenic in the Bengal delta. However, the concentrations of Fe and Mn weakly correlate with As contents, whereas Al contents show no relationship with As. The results of this study suggest that reactive oxides or hydroxides of Fe and Mn, rather than Fe and Mn with other minerals, might control arsenic distribution.  相似文献   

17.
Vertical profiles from the water column, including the maximum turbidity zone (MTZ) to the consolidated sediment were sampled in September 2000 in the freshwater reaches of the Gironde Estuary during a complete neap tide-spring tide cycle. The vertical distributions of dissolved major redox parameters and metals (Mn, Fe, Cd, Cu, V, Co, Ni, Mo, and U) were determined. Reactive particulate metal fractions were also determined from selective leaching. The studied system is characterized by density layers functioning at different time-scales, consisting of two mobile layers, i.e., the liquid (LM) and the soft mud (SM), overlying consolidated sediments (CS). This results in a three-zone diagenetic regime where (1) O2 dynamics are fast enough to show depletion in the rapidly mixed LM sequence (tidal time-scale), (2) denitrification occurs on the weekly time-scale mixing SM sequence, and (3) the Mn, Fe, and sulfate cycling occurs in the CS layer (annual time-scale). The studied trace metals show differential behavior during early diagenesis: (1) Cd, Cu, and V are released into pore water preferentially from organic matter in the SM, (2) Co, Ni, and U are released in the CS from Mn and Fe oxides during reductive dissolution, and (3) Mo from both processes. Transient conditions (i.e., oscillations of redox fronts and reoxidation processes), due to the dynamics of the mobile layers, strongly influence the trace metal distributions as inducing resolubilization (Cd, Cu, and Mo). In the CS, authigenic metal phases accumulate, either by direct precipitation with sulfides (Cu, Cd) or co-precipitation with Fe-sulfides (Mo). Microbially mediated reduction of Fe oxides is proposed to control U removal from pore water by reduction of U(VI) to U(IV) at depth. However, a significant fraction of the trace metals is trapped in the sediment in exchangeable forms, and therefore is susceptible to be mobilized due to resuspension of estuarine sediment during strong river flood periods and/or dredging activities.  相似文献   

18.
Enrichments of REY (rare earth + yttrium) and other trace metals (Co and Ni) in deep-sea ferromanganese (FeMn) micronodules have received increasing attention in both deep-sea research and mineral exploration. Due to the presence of multiple, easily-crushed and poorly-crystallized phases in micronodules, the genesis of micronodules and their adsorption of various trace elements are poorly understood. To address this gap, we examined the spatial distributions of elements in cross-sections of micronodules from the western tropical North Pacific Ocean using high-resolution (HR) LA-ICP-MS raster mapping coupled with laser Raman and X-ray photoelectron spectroscopy (XPS). The ferromanganese micronodules we studied are dominated by Fe and Mn oxides with minor carbonate minerals, such as siderite, rhodochrosite and calcite. LA-ICP-MS maps show that these micronodules consist of a Mn-rich core and a Fe-rich rim. The Fe-enriched rim is enriched in As and surrounds a Mg, Mn, Cu, Co and Ni concreted core. Laser Raman maps show that the micronodule core contains more birnessite, an important scavenger of trace metals in deep sea sediments, than the rim. The birnessite filled core of these micronodules does not have elevated REY. Indeed, birnessite line channels may feed metal-rich fluid containing REY to adjacent minerals, including well-crystallized bio-apatite and zeolite, as high Ce and Y levels are spatially correlated with these minerals. The observed element profiles and XPS observations showing the coexistence of multiple oxidation states of Mn (+2, +3 and +4), Fe (+2 and +3) and Ce (+3, +4) demonstrate that the FeMn phases of these micronodules are of a diagenetic origin and that they are sites of redox-driven metal enrichment in deep-sea sediment.  相似文献   

19.
The occurrence of early diagenetic Ca‐rhodochrosite [(Mn,Ca)CO3] is reported in association with ‘griotte’‐type nodular limestones from basinal settings in the geological record; however, without the comparison of analogous modern examples, the controls on precipitation remain speculative. Here the findings of four layers of primary Ca‐rich rhodochrosite recovered from a modern deep‐sea setting in the Eastern Equatorial Pacific, from bioturbated sediments 300 m below sea floor, are reported (Ocean Drilling Program, Leg 201, Site 1226). The mineralogy is similar to cements in burrows recovered during Deep Sea Drilling Project Leg 68 at Eastern Equatorial Pacific Site 503 and from Ca‐rhodochrosite laminae in sediments of the central Baltic Sea. Petrographic relationships and constant oxygen isotopic compositions in the Ca‐rhodochrosite around 5‰ at all depths indicate a shallow burial depth of formation. The onset of 1‰ heavier oxygen isotope composition of Ca‐rhodochrosite at Site 503, about 30 m below the Pliocene/Pleistocene boundary, further suggests that precipitation occurs in the range of 30 m below sea floor. The approximate depth of formation allowed an approximate empirical fractionation factor for marine Ca‐rhodochrosite to be constrained that strongly differs from previously published theoretical values. Based on the approximate precipitation depth, authigenic Ca‐rhodochrosite forms within the SO42?‐reduction zone. Moderately negative δ13C values (around ?3‰) and total organic carbon lower than 2 wt% indicate a relatively low contribution of CO32? from organic C mineralization within the expanded redox zonation in the Eastern Equatorial Pacific. It is suggested that the alkalinity is increased by a rise in pH at focused sites of Mn‐reduction coupled with S2? oxidation. High concentrations of Mn‐oxide can accumulate in layers or burrows because of Mn‐cycling in suboxic sediments as suggested for the Baltic Sea Ca‐rhodochrosites. This study demonstrates how early diagenetic precipitates document biogeochemical processes from past diagenetic systems.  相似文献   

20.
Increased development and changing climate have enhanced global interest in the Arctic Ocean and adjacent seas. Using a large, 3-yr data base, we have determined the distribution of trace metals in sediments from the inner shelf of the western Beaufort Sea. Metal concentrations in these sediments reflect pristine conditions, consistent with those for most coastal areas in the Arctic and with predictions based on average continental crust. Geographic variations in metal values are primarily related to sediment grainsize distribution. However, grain-size patterns are a complex function of several variables including source areas, ice and water movement, as well as physical and chemical weathering. Future identification of any metal contamination in Beaufort Sea sediments will be simplified by understanding the predictable natural patterns.  相似文献   

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