首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 838 毫秒
1.
This paper focuses on characterizing the current status of physical and chemical characteristics of King Talal Dam (KTD) sediments. The quality of sediments was investigated based on several international sediment quality guidelines. The volume of sediment and sedimentation rate in (KTD) was also estimated. Five types of granulometric textural facies were observed for the sediments of KTD reservoir bed, with an average grain size distribution of gravel (1.38%), sand (32.38%), silt (32.35%) and clay (32.38%). The fraction of <63 micron showed that the total mean size was 8.0 micron. Other sediment parameters in KTD were 7.0% for total organic matter (TOM), 7.3 for pH, 35.9% for CaCO3 and 100.5 meq/100 g for cation exchange capacity, with dominant mineralogical constituents of quartz, calcite, dolomite, clay minerals and minor feldspar. The total concentrations of F, Cl, NO2, NO3, PO4 and SO4 in sediment samples were lower inward for KTD. The vast majority of trace metals in sediments were generally within the standard limits recommended for soils. TOM and grain size of sediment are major factors governing the trace metal concentrations. The calculated geoaccumulation index (I geo) and enrichment factor of metals in bottom sediments showed that the metals were in the following order: Cd > Pb > Zn > Co > Cr > Ni > Fe > Cu > Sr > Mn and Cd > Zn > Pb > Co > Cr > Ni > Cu > Sr > Mn, respectively. Based on the sonic survey of KTD reservoir, the annual sedimentation rate was about 0.4061 MCM/year, in which about 18.66% of the reservoir initial storage capacity was lost to sediments and a projected lifespan of about 198 years.  相似文献   

2.
长江口及邻近海域表层沉积物pH、Eh分布及制约因素   总被引：8，自引：1，他引：7  
使用精密酸度计和新型全自动氧化还原电位仪测定了长江口及其临近海域表层沉积物中的pH、Eh值,分析了它们的分布特征,并从水团性质、层化特征、底质类型、生物扰动等方面深入探讨了pH、Eh的影响因素和影响机理。研究表明:研究区内表层沉积物属于中性—弱碱性环境,pH值变化于7.1～7.8之间,空间分布上具有分带性和不均一性特征;为还原环境,Eh变化于-100～-300 mV之间,大部分在-250 mV左右,其空间分布也具有弱分带和不均一的特点。该区沉积物酸碱性主要受水团性质的制约,同时底质类型、生物扰动对沉积物酸碱性也有一定影响,而氧化还原电位则主要受水团性质、水层层化和生物扰动等的影响。  相似文献   

3.
Understanding the effects of organic acids (OA) on the transformation of Fe and Mn to surface water from the weathering coal gangue is of great benefit to risk assessment and remediation strategies for contaminated water and soil. Based on the investigation on surface water in the central coal districts of the Guizhou Province, 18 water samples were collected for heavy metal analysis. The results indicated that the pH value of surface water is low (3.11–4.92), and Fe concentration (1.31–5.55 mg L?1) and Mn concentration (1.90–5.71 mg L?1) were, on average, 10.86 and 34.33 times the limit of Surface Water Quality Standards, respectively. In order to evaluate the effects of the OA on the dissolution of Fe and Mn from the weathering coal gangue, column elution and batch leaching experiments were conducted. The results show that the low molecular weight of organic acids (LMWOAs, i.e., oxalic, tartaric, malic and citric acids) and fulvic acids significantly accelerated the dissolution of Fe and Mn; in addition, when the concentration of OA reached 25 mmol L?1, the concentrations of Fe, and Mn were 1.14–67.08 and 1.11–2.32 times as high as those in 0.5 mmol L?1 OA, respectively. Furthermore, the migration of Fe and Mn was significantly influenced by the pH and Eh, especially for Fe; the ion Mn was dissolved from the gangue more easily than the ion Fe in the column leaching, which was contrary to the results of batch leaching.  相似文献   

4.
The sediment cores of 20 cm length collected from 31 to 83 m range of water depth from the inner shelf of Bay of Bengal west of “Swatch of No Ground” were analyzed for grain size, organic carbon, total nitrogen, calcium carbonate and clay mineralogy. Grain size analysis revealed that the sediment size decreases from west to east within the study area indicating a possible direction of transport towards east parallel to the coast. The grain size also decreases with increasing water depth, i.e. north to south, indicating sediment contribution to the area of study from Hooghly and other local rivers. In the cores studied, illite was the dominant clay mineral which seems to be a product of glacial weathering under arid conditions with its source being the Himalayan region. The organic carbon content was low in the sediments and was attributed to low plankton production or intense oxidation processes. Low calcium carbonate percentage also supports the view of a low productivity in this region. Organic carbon increases gradually from west to east indicating its association with finer sediments and also indicates transport due to currents which drift the organic carbon away before it settles down within the sediments. Higher values relatively closer to the coast in the eastern side indicate additional contribution from Sunderban mangroves. The C/N ratio obtained indicates mixed source of terrestrial and marine for the organic matter in the sediments. Sedimentation rates available for deltaic plains and shelves off Bangladesh when adopted for the present area revealed that a 20 cm long sediment column was deposited in around 10 years. In most of the cores studied, a change in the trend of sediment components and organic carbon was observed at around 10 cm where grain size increases and organic carbon decreases towards the surface inferring that during the last 5 years, possible floods during NE monsoon or due to melting of ice in Himalaya are responsible for releasing additional water and material which brought a change in hydrodynamic conditions. The surface depletion of organic carbon indicates its dilution by the addition of coarser materials.  相似文献   

5.
The New York Bight is a sector of the Middle Atlantic continental shelf. The Bight consists of a part of the Atlantic Ocean offshore of the New York and New Jersey metropolitan area. This area includes the most populated coastal setting in North America. The Atlantic shelf and its estuaries are used for waste disposal, dredging, commercial fishing, and recreation; activities that contribute to the contamination of associated bottom sediments. Existing data for toxicants are still inadequate. Improvements in sediment and water quality will require a more detailed knowledge and understanding of sediments and water in the Bight. Eleven coring stations were established in New York Bight. Decreases in pH and Eh both above and below the water/sediment interface are attributed to the activity of anaerobic bacteria. Sulfate reduction is one of the important processes in lowering pH. Low Eh values of up to −443 can be related to sulfate-reducing bacteria. The highest negative Eh generally occurs with the highest organic carbon concentration. Core samples yielded up to 4.00% organic carbon compared to 0.8 to 1.2% in sediments of the natural nearshore environment. Twenty-seven different aliphatic hydrocarbons, fourteen PAHs, five cyclic hydrocarbons, and eight dicarboxylic acids were identified in the Bight pore waters. Sediment located deeper in the Hudson Shelf Valley has a greater abundance of aliphatic hydrocarbons as adsorbed pollution on clay and silt. The presence of dicarboxylic acids leached from plastic came from anthropogenic activities (mostly sewage). PAHs have two sources: coal ash (observed in sediments) and petroleum (part of the sewage, run-offs, and oil spills). The rest of the hydrocarbons have a petroleum or biogenic origin. The high amount of organic carbon may be the result of sewage sludge or originated from natural sources. The main sources of contaminants are dumpsites, emergency releases after heavy rainstorms from sewage-treatment plants, tanker washing, storage transfer spills, run-off, and air-borne pollution. The relatively high accumulation of organic matter causes oxygen depletion, which creates anaerobic conditions. The presence of hydrogen sulfide makes the environment toxic for most of the biota. Detected hydrocarbons, especially PAHs easily enter the food chain and may cause cancer and mutagenic reactions of biota and humans. Organic petrology of six organic-rich sediments from New York Harbor illustrates a diverse population of anthropogenic and natural organic components. Three core samples (V-2, AC-4, and HV-3) contain coarse-textured organic matter. A slim majority of those components are anthropogenic. They are derived mainly from coal combustion by-products. The other two core samples (AC-6 and T-1) contain mainly very fine-grained organic matter. A majority of them are amorphous organic matter (AOM) that is derived from bacterial degradation of modern organic matter. Radionuclide dating (137Cs, K-40, Pb-210) shows post-1950 components for the shallowest intervals in the cores (<30 cm). The post-1950 sediment, distributed in the tops of core, is recycled material from the dumpsites. The underlying sediment has isotopic signatures that suggest dates before active dumping.  相似文献   

6.
This study reports the first ethanol and acetaldehyde measurements in sediment porewaters collected at multiple freshwater locations. Ethanol concentrations ranged from 11 to 2535 nM and acetaldehyde concentrations ranged from 6 to 320 nM. A significant positive correlation (p < 0.001) was observed between ethanol concentrations and the percent organic carbon content of sediments (TOC). Porewater depth profiles at two sites within the same lake indicated potential diffusion of ethanol into sediments from the overlying water at a lower TOC site and upwards diffusion from sediment into the water column at a higher TOC site. Diffusion of water column ethanol into sediments was observed at individual sites from October to January, whereas the opposite was true from June to August indicating the seasonal variability of ethanol flux from sediments. Changes in ethanol concentrations during a long-term sediment incubation experiment showed an inverse relation with acetaldehyde concentrations. The lack of a quantitative conversion was likely due to other sources and sinks that control their abundance. Our study provided new information on the biogeochemistry of ethanol in freshwater sediments and shed light on the potential role of ethanol in the global carbon cycle.  相似文献   

7.
This study addresses the distribution of total phosphorus (TP) and its inorganic (IP) and organic (OP) fractions, grain-size and organic matter of surface and recent sediments, coupled to the behavior of total and dissolved inorganic phosphorus (TP and DIP) of the water column, of the semi-pristine Guaratuba Bay estuary, SE Brazil. Surface sediment samples were taken at 43 sites spread along the estuarine gradient and recent sediments from 3 short (35 cm long) cores from the upper, central and lower portions of the estuary, respectively. Highest TP and IP concentrations of surface sediments were detected within the upper sector and the transition zone between the upper and central sectors, all characterized by fine sediments, low salinities and water depths. In contrast, the lower sector and its narrow and deep tidal channel, subject to more intense tidal forcing, exhibited a higher fraction of sandy sediments with lower TP, IP and OP contents. In spite of the spatial variability in sediment grain size, IP corresponded to the major fraction of TP in all estuarine sectors and both TP and IP correlated significantly with the fine sedimentary (silt + clay) grain-size fraction. The fine surface sediments acted as a trap for IP at the fresh water–low salinity interface, which also corresponded to the region of a DIP sink in surface waters. In general, the short sediment cores showed that TP and IP contents increased from 15 cm depths to the top layer. Published sedimentation rates from additional cores taken at the sites of the short cores of this study, implied that depositional alterations of TP and IP increased during the early 1970s, which corresponded to the onset of anthropogenic disturbances from crop plantations in the lowland plains of the river end-member and urbanization at the estuary’s mouth and along the adjacent coast.  相似文献   

8.
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   

9.
Iron and manganese in bottom sediments studied along the sublatitudinal transect from Kandalaksha to Arkhangelsk are characterized by various contents and forms depending on sedimentation environments, grain size of sediments, and diagenetic processes. The latter include redistribution of reactive forms leading to enrichment in Fe and Mn of the surface sediments, formation of films, incrustations, and ferromanganese nodules. Variations in the total Fe content (2–8%) are accompanied by changes in the concentration of its reactive forms (acid extraction) and the concentration of dissolved Fe in the interstitial water (1–14 μM). Variations in the Mn content in sediments (0.03–3.7%) and the interstitial water (up to 500 μM) correspond to a high diagenetic mobility of this element. Changes in the valence of chemical elements results in the redox stratification of sediment strata with maximum concentrations of Fe, Mn, and sulfides. Organic matter of sediments with a considerable terrestrial constituent is oxidized by bottom water oxygen mainly at the sediment surface or in anaerobic conditions within the sediment strata. The role of inorganic components in organic matter oxidation changes from surface sediments, where manganese oxyhydroxide dominates among oxidants, to deeper layers, where sulfate of interstitial water serves as the main oxidant. Differences in river runoff and hydrodynamics are responsible for geochemical asymmetry of the transect. The deep Kandalaksha Bay serves as a sediment trap for manganese (Mn content in sediments varies within 0.5–0.7%), whereas the sedimentary environment in the Dvina Bay promotes its removal from sediments (Mn 0.05%).  相似文献   

10.
Lake Houston is a man-made reservoir located northeast of Houston, Texas. The purpose of this investigation was to document suspended sediment transport, sedimentation, and resuspension in the lake with a view towards estimating the influence of sedimentation on water quality. Sediment traps were placed in strategic locations in the lake to collect suspended sediments. Samples were analyzed for bulk density, grain size, organic carbon, and a number of trace elements. These data were analyzed along with meteorological data to examine those factors which regulate suspended sediment input and dispersal, and the role of suspended sediments in controlling water quality within the lake. Sediment input to the lake depends primarily on the intensity of rainfall in the watershed. Sediment movement within the lake is strongly influenced by wave activity, which resuspends sediments from shallow areas, and by wind-driven circulation. The increased residence time of suspended sediments due to resuspension allows greater decomposition of organic matter and the release of several trace elements from sediments to the water column. Virtually all samples from sediment traps suspended between 1 and 5 m above the lake bottom contain medium to coarse silt, and even some very fine sand-sized material. This implies that circulation in Lake Houston is periodically intense enough to transport this size material in suspension. During winter, northerly winds with sustained velocities of greater than 5 m/sec provide the most suitable condition for rapid (<1 d) transport of suspended sediment down the length of the lake. Fluctuations in current velocities and the subsequent suspension/deposition of particles may explain variations in the abundance of coliform bacteria in Lake Houston.  相似文献   

11.
The western Arctic Shelf has long been considered as an important sink of nitrogen because high primary productivity of the shelf water fuels active denitrification within the sediments, which has been recognized to account for all the nitrogen (N) removal of the Pacific water inflow. However, potentially high denitrifying activity was discovered within the oxygenated Chukchi Shelf water during our summer expedition. Based on 15N-isotope pairing incubations, we estimated denitrification rates ranging from 1.8 ± 0.4 to 75.9 ± 8.7 nmol N2 L?1 h?1. We find that the spatial pattern of denitrifying activity follows well with primary productivity, which supplies plentiful fresh organic matter, and there was a strong correlation between integrated denitrification and integrated primary productivity. Considering the active hydrodynamics over the Chukchi Shelf during summer, resuspension of benthic sediment coupled with particle-associated bacteria induces an active denitrification process in the oxic water column. We further extrapolate to the whole Chukchi Shelf and estimate an N removal flux from this cold Arctic shelf water to be 12.2 Tg-N year?1, which compensates for the difference between sediment cores incubation (~ 3 Tg-N year?1) and geochemical estimation based on N deficit relative to phosphorous (~ 16 Tg-N year?1). We infer that dynamic sediment resuspension combined with high biological productivity stimulates intensive denitrification in the water column, potentially creating a nitrogen sink over the shallow Arctic shelves that have previously been unrecognized.  相似文献   

12.
Monsoon-induced coastal upwelling, land run-off, benthic and atmospheric inputs make the western Indian shelf waters biologically productive that is expected to lead to high rates of mineralisation of organic matter (OM) in the sediments. Dissimilatory sulphate reduction (SR) is a major pathway of OM mineralisation in near-shore marine sediments owing to depletion of other energetically more profitable electron acceptors (O2, NO3 ?, Mn and Fe oxides) within few millimetres of the sediment-water interface. We carried out first ever study to quantify SR rates in the inner shelf sediments off Goa (central west coast of India) using the 35S radiotracer technique. The highest rates were recorded in the upper 10 cm of the sediment cores and decreased gradually thereafter below detection. Despite significant SR activity in the upper ～12 to 21 cm at most of the sites, pore water sulphate concentrations generally did not show much variation with depth. The depth integrated SR rate (0.066–0.46 mol m?2 year?1) decreased with increasing water depth. Free sulphide was present in low concentrations (0–3 μM) in pore waters at shallow stations (depth <30 m). However, high build-up of sulphide (100–600 μM) in pore waters was observed at two deeper stations (depths 39 and 48 m), 7–11 cm below the sediment-water interface. The total iron content of the sediment decreased from ～7 to 5 % from the shallowest to the deepest station. The high pyrite content indicates that the shelf sediments act as a sink for sulphide accounting for the low free sulphide levels in pore water. In the moderately organic rich (2–3.5 %) sediments off Goa, the measured SR rates are much lower than those reported from other upwelling areas, especially off Namibia and Peru. The amount of organic carbon remineralised via sulphate reduction was ～0.52 mol m?2 year?1. With an estimated average organic carbon accumulation rate of ～5.6 (±0.5) mol m?2 year?1, it appears that the bulk of organic matter gets preserved in sediments in the study region.  相似文献   

13.
An exploratory study was carried out at 22 sampling stations along the Langat River, Selangor in order to investigate on the vitality of cation exchange capacity (CEC) in sediment (0–5 cm). Parameters such as pH, Eh, salinity, and electrical conductivity (EC) were determined. The CEC in sediment has been calculated by the determination of Ca2+, Na+, Mg2+, and K+ using the flame atomic absorption spectrophotometer, while the organic matter content in sediment was ascertained using the loss on ignition method. The characteristic of the sediment shows that pH (3.09–7.46), salinity (0.02–10.71 ppt), EC (3.39–517 μS/cm) and Eh (?16.20–253.10 mV) were substantially high in variation. This study also revealed that exchangeable Ca2+ and Mg2+ were controlled by organic matter contents, while exchangeable Na+ and K+ were influenced by salinity. Salinity was observed to play a major part in controlling all the exchangeable cations, as it gives strong significant correlations with Na+, K+, Mg2+, CEC, and organic matter at p?<?0.01. The presence of seawater, clay mineralogy, and organic matter proves that it does play an important role in determining the CEC and soon relates to the pollution magnitude in the sediment.  相似文献   

14.
孙云明  宋金明 《地质论评》2001,47(5):527-534
海洋沉积物中的N和P随沉积物的粒度由粗到细,含量逐渐升高,而Si则降低;积物中N、P、Si的含量还随海区、输入源、季节、动力学过程及生物生产过程不同而变化.控制海洋沉积物-海水界面N、P、Si沉积、释放及循环的因素,包括有机质和溶解氧的浓度、有机质中C、N、P、Si的相对比例、沉积物-海水界面附近的氧化还原环境、生物扰动、温度、水深、pH值、不同形态S的浓度、金属离子以及水动力条件等.一般其综合作用的表现是,沉积物-海水界面之间NH+4、PO3-4和Si(OH)4从沉积物向上覆水扩散转移,而硝酸盐和亚硝酸盐的通量方向相反,通量的大小随着海区的不同差别较大.  相似文献   

15.
The study area lies between 31.32°N, 31.70°E and 31.41°N, 31.78°E along Damietta branch, Nile River. It is about 24-km long. Acoustic classification (Quester Tangent Corporation—QTC) is used as a powerful tool to study seabed characteristics which is confirmed by the sediment analyses. Sediment characteristics of the study are presented by three acoustic classes: sand, mud and organic matter intercalated by clay. The depth varies from about ?12 m at Faraskour Bridge (southern part of the study area) to about ?2.5 m at Faraskour Dam (northern part of the study area). The average current velocity is detected as 4 cm/s and it has a very low effect on the transport of both sediment and waste debris. The sediment in the northern part characterized by organic matter reaches about 70 cm thickness under and around fish cages. This huge amount of organic matter deposit leads to the reduction of the dissolved oxygen and increase pH values. This study shows that the water quality in the northern part of the study area is at risk (drinking water for Damietta city) due to the presence of the huge amount of waste debris intercalated by organic matter. The rises of temperature in summer enhance oxygen consumption and the decomposition of the organic matter. This is rapidly increasing the growth of bacteria and phytoplankton, causing turbidity and algal blooms. Those affect the water quality and raise the water toxicity (drinking water).  相似文献   

16.
Damming of the North Anna River in 1972 created Lake Anna, a cooling water source for the Dominion nuclear power plant as well as a popular recreation site in Spotsylvania and Orange counties, Virginia, USA. Previously dated (210-Pb) sediment cores from seven locations within the lake and three locations in the adjoining Waste Heat Treatment Facilities (WHTF) were analyzed for trace metals (Al, Ba, Zn, Cd, Cu, Fe, Mn and Pb) and polychlorinated biphenyls (PCBs) to examine the environmental evolution of the reservoir system. The reservoir has a history of mining activities in its watershed and unusually elevated concentrations of PCBs were found in fish tissues from previous studies. Therefore, dated sediment cores provided the framework for both the temporal and spatial analysis of possible sources and flux histories for both trace metals and PCBs. The trace metals results suggest that, though the upper reaches are relatively less impacted, the old mine tailings from the now ceased mining activities in the watershed of Contrary Creek tributary continue to dominate the sediment chemistry of the lower portion of the lake basin, signified by sediment enrichment of Pb, Cd, Cu, and Zn. Lagoon-2 of the WHTF also seems to be receiving unusually high loadings of Cd (12.5 ± 1.07 μg/g) that is probably associated with waste materials from the nuclear power plant that maintains the lagoons. PCB sediment concentrations were relatively low in the lower sections of the basins with values typically being <3.5 ng/g. The upper reaches of the basin had several PCB hotspots, with the surface sediments of Terry’s Run tributary having values as high as 53.13 ng/g. The spatial distribution of PCBs seems to suggest the upper reaches of the basin as the probable source, with the unusually high concentrations near bridges suggesting a possible link between the PCBs and old bridge fill materials. The oldest lacustrine sediments also had relatively high trace metals and PCB values signifying a probable role of soil disruption and sediment reconcentration during reservoir construction.  相似文献   

17.
The distribution of Mn was examined in the bottom sediments and water column (suspended paniculate matter) of the Laurentian Trough. Gulf of St. Lawrence. A characteristic profile of Mn with depth in the sediment consisted of a Mn-enriched surface oxidized zone, less than 20 mm thick, and a Mn-depleted subsurface reducing zone. A subsurface Mn maximum occurred within the oxidized zone. Below this maximum the concentration dropped sharply to nearly constant residual levels in the reducing zone. The accumulating estuarine sediments are deficient in Mn compared to the river input of suspended matter and are definitely not the ultimate sink for manganese. Manganese escapes from the sediment by diffusion and resuspension, forming Mn-enriched, fine-grained particles which are flushed out in the estuarine circulation. 5.0 × 109gyr?1 of Mn, or 50% more than the river input of dissolved Mn. are exported to the open ocean. In spite of the efficient mobilization and export of Mn, the quantity exported is a small fraction (0.2%) of the total flux to the deep-sea sediments. This is related to the low levels of paniculate matter transported by the St. Lawrence River. The export phénomenon, however, is probably true of many coastal regions of muddy sediments and thus has interesting implications for the oceanic budget of Mn.  相似文献   

18.
We present inorganic geochemical analyses of pore waters and sediments of two Late Quaternary sediment cores from the western Arctic Ocean (southern Mendeleev Ridge, RV Polarstern Expedition ARK-XXIII/3), focussing on the composition and origin of distinct, brown-colored, Mn-rich sediment layers. Carbonate enrichments occur in association with these layers as peaks in Ca/Al, Mg/Al, Sr/Al and Sr/Mg, suggesting enhanced input of both ice-rafted and biogenic carbonate. For the first time, we show that the Mn-rich layers layers are also consistently enriched in the scavenged trace metals Co, Cu, Mo and Ni. Distinct bioturbation patterns, specifically well-defined brown burrows into the underlying sediments, suggest these metal enrichments formed close to the sediment-water interface. The geochemical signature of these metal- and carbonate-rich layers most probably documents formation under warmer climate conditions with an intensified continental hydrological cycle and only seasonal sea ice cover. Both rivers and sea ice delivered trace metals to the Arctic Ocean, while enhanced seasonal productivity exported reactive organic matter to the sea floor. The coeval deposition of organic matter, Mn (oxyhydr)oxides and trace metals triggered intense diagenetic Mn cycling at the sediment-water interface. These processes resulted in the formation of Mn and trace metal enrichments, and the degradation of labile organic matter. With the onset of cooler conditions, reduced riverine runoff and/or a solid sea ice cover terminated the input of riverine trace metal and fresh organic matter, resulting in deposition of grayish-yellowish, metal-poor sediments. Oxygen depletion of Arctic bottom waters under these cooler conditions is not supported by our data, and did not cause the sedimentary Mn distribution. While the original composition and texture of the brown layers resulted from specific climatic conditions and corresponding diagenetic processes, pore water data show that diagenetic Mn redistribution is still affecting the organic-poor deeper sediments. Given persistent steady state conditions, purely authigenic Mn-rich brown layers may form, while others may be partly or completely dissolved. The degree of diagenetic Mn redistribution largely depends on the depositional environment, the Mn and organic matter availability, and apparently affected the Co/Mo ratios of Mn-rich layers. Thus, brown Arctic layers are not necessarily synchronous features, and should not be correlated across the Arctic Ocean without additional age control.  相似文献   

19.
The presence of arsenic (As) in surface water constitutes an important environmental risk, where mobility and adsorption processes are responsible for its behavior in the sediment–water interface. Therefore, the assessment of adsorption, mobility and water availability of arsenic in freshwater sediments, with agricultural, livestock and urban soil uses was performed. Arsenic concentrations in sediments ranged from 5.4 to 15.9 mg kg?1 (total) and 2.8 to 6.5 mg kg?1 (labile), and those of iron and manganese were 11,563–23,500 and 140.6–662.1 mg kg?1, respectively. The As levels in water were significantly lower than those of sediments. Results would suggest that As co-precipitation and adsorption on Fe oxides are probably the major route of immobilization, determining its low lability. Manganese did not present an outstanding contribution to the retention, and cation-exchange capacity, pH and organic matter of sediments did not show an influence on the mobility of As.  相似文献   

20.
Organic matter was isolated from the water columns and sediments of two pond systems in the south-eastern United States. Water column material was ultrafiltered to provide three fractions, i.e. <0.45 μm, but > 50,000 daltons; <50,000 daltons, but > 5000 daltons; and <5000 daltons. Sedimentary organic matter was separated into humic acid and fulvic acid fractions based on solubility criteria and the humic acid fraction was ultrafiltered to provide the same fractions as the water column isolates. All fractions were analysed for organic carbon, Al, Ca, Cu, Fe, Mg and Mn. Infra-red spectra were also measured for the sedimentary organic fractions. Organic matter isolated from the water column of the two ponds had similar organic carbon and elemental distributions, as did the organic matter isolated from the two sediments. However, significant differences in the organic carbon and elemental distributions were observed for water column and sedimentary organic matter isolated from the same pond. These studies have relevance to diagenetic alterations of organic matter and geochemical cycles of elements within lakes.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号