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1.
北黄海沉积速率及其沉积通量 总被引：10，自引：3，他引：10
黄海大陆架沉积物多来自黄河的输入,区域性环流模式控制着这些沉积物的输送过程。目前对浅海陆架沉积物沉积过程和沉积环境的研究很少,尤其是北黄海沉积物的堆积过程和沉积通量。我们对9个沉积岩心进行了210Pb分析测定,绘制了210Pb活度的垂直分布图,并计算了沉积通量,北黄海沉积通量为0 06～1 18g/(cm2·a),北黄海中部泥质区沉积通量低于0 33g/(cm2·a)。大多数的210Pb垂直分布呈两层分布模式,不同的垂直分布反映了水动力和沉积过程的时空变化。为了评价北黄海的物源和沉积环境,测定了10个表层沉积物样品的化学元素含量,测定结果表明北黄海泥质区沉积物是多源沉积,但其主要来源还是黄河的输入。 相似文献
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末次盛冰期以来冲绳海槽中部沉积物有机碳和磷的地球化学研究 总被引：1，自引：0，他引：1
利用元素及同位素地球化学方法研究了冲绳海槽中部沉积物岩芯中有机碳及磷的地球化学特征及影响因素。结果表明，冲绳海槽沉积速率（16.5~32.5 cm/ka）变化小，不是沉积物中有机碳埋藏的重要影响因素。相对于全新世氧化性底水环境，末次盛冰期/冰消期冲绳海槽缺氧底水环境提高了沉积物对有机碳的埋藏效率。冲绳海槽沉积物中各形态磷的相对含量与其他边缘海沉积物中的相似。交换态磷（Ex-P）含量低、变化小。末次盛冰期/冰消期缺氧底水环境下铁氧化物的还原溶解导致铁结合磷（Fe-P）释放以及自生磷矿物（Au-P）的形成。全新世氧化性底水条件有利于铁氧化物的有效再生及对磷的再吸附，但不利于Au-P的保存。总有机碳（TOC）和有机磷（Org-P）之间良好的相关性表明TOC埋藏对Org-P含量的重要控制作用。冲绳海槽沉积物中碎屑磷（De-P）含量低于长江口及东海陆架沉积物中的含量，这与陆源碎屑向外海传输减弱有关。在约9.3 ka BP（岩芯200 cm深度），TOC、Fe-P、Org-P、De-P以及FeHR均出现的极小值可能由物质坡移造成。 相似文献
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胶州湾现代沉积速率和沉积通量研究 总被引：19，自引：0，他引：19
对胶州湾沉积岩心J39、J37和J94进行了210Pb的测定,绘制了岩心中210Pb的垂直分布图,岩心J37和J94的210Pb呈两段分布模式,岩心J39的210Pb呈三段分布模式。胶州湾西北部大沽河口外海域近百年来沉积速率为0 768cm/a,沉积通量为0 7716g/(cm2·a)。胶州湾中部沉积速率为0 64cm/a,沉积通量为0 65g/(cm2·a)。胶州湾口外J94站沉积速率为0 54cm/a,沉积通量为0 81g/(cm2·a)。结果表明,胶州湾海域210Pb活度与悬浮体含量密切相关,悬浮体含量高的区域,210Pb活度高;反之,悬浮体含量低的区域,210Pb活度低。根据210Pb的垂直分布、活度和沉积速率及悬浮体含量,结合历史资料,对胶州湾近百年来的沉积环境和物质扩散进行了探讨。 相似文献
5.
海州湾南部近岸现代沉积速率及其沉积通量 总被引：1，自引：0，他引：1
对海州湾南部近岸3个柱状岩芯进行了210Pb的测定,绘制了岩芯中210Pb的垂直分布图。结果表明,柱-1岩芯表现为2个明显的沉积阶段,1-12 cm平均沉积速率为0.51 cm/a,12-57 cm的为0.18 cm/a,沉积通量分别为0.69和0.24 g/（cm^2·a）;柱-2岩芯平均沉积速率为0.64 cm/a,沉积通量为0.68 g/（cm^2·a）;柱-3岩芯平均沉积速率为0.67 cm/a,沉积通量为0.76 g/（cm^2·a）。沉积速率从北往南逐渐增大。造成这种空间分布规律的主要因素是沉积环境和物质来源,其次可能同海域位置、沉积物组分特征和海底地形有关。 相似文献
6.
东海表层水体中的多环芳烃及其沉积通量估算 总被引：2，自引：0，他引：2
以东海陆架水体中溶解态多环芳烃(PAHs)含量为基础,引入颗粒相-水相间的物质吸附系数(Koc)计算悬浮颗粒物中PAHs有机碳归一化含量,结合陆架沉积物有机碳的年埋藏通量,估算东海陆架沉积物中PAHs沉积通量。结果显示:水体中溶解态的15种PAHs总含量为(701±392)ng/L,变化范围为412~1 032ng/L,PAHs组成以3环为主。计算得到的悬浮颗粒物中15种PAHs有机碳归一化含量为20~28μg/g,对应的PAHs沉积通量为150~210t/a。估算结果与实测沉积物中PAHs含量和沉积通量结果基本吻合,表明实验室模拟实验获取的化合物Koc值适用于东海颗粒相-水相间的分配模型,证实悬浮颗粒物有机碳含量在控制PAHs两相分布过程中起着重要作用。同时,该方法为海洋沉积物中PAHs沉积通量的估算提供一种新途径。 相似文献
7.
海洋沉积物中碘的早期成岩再迁移 总被引：2，自引：1，他引：2
本文在笔者多年的南大洋沉积地球化学研究的基础上,从碘的相态变化着手,结合其他沉积地球化学参数,讨论了以南大洋区域为主的海洋沉积物中碘的早期成岩再迁移过程。结果表明,碘的早期成岩迁移过程并不像过去常认为的那样几乎完全由有机质控制。在研究区域的陆架和半深海表层沉积物中碘的吸附相和氧化物结合相平均分别可占23%和32%。表层沉积物I/Corg.值除与沉积有机的沉降条件有关外,还取决于沉积柱深处碘向上扩散的强度和沉积物的氧化还原条件。实验结果亦证实了氧化物结合相和吸附相在沉积柱中的再迁移可导致I/Corg.值随深度的增加而降低的现象。进一步的计算表明,沉积柱深处往上扩散的通量与海水中沉积碘的通量处于同一数量级水平,这可能是沉积岩贫碘的重要原因。基于上述讨论和计算结果,笔者提出了海洋沉积物中碘的早期成岩再迁移模式。 相似文献
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利用1984年夏季的现场调查,作者研究了黄河口及邻近海域表层沉积物中铜的地球化学形式。含量及其分布,分析了铜和有机质、铁、锰、锌及中值粒径之间关系,并指出总铜平均含量为20.4mg/kg.其中残渣部分占55％,有机结合铜为19.4％、Fe-Mn氧化物结合铜为12.1％、碳酸盐结合铜为13.1％,可交换铜的含量小于1％。此外讨论了沉积物中各种形式铜含量与铁、锰、有机质及中值粒径关系。 相似文献
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根据交换速率连续函数计算法,应用实验室培养法测定了PO_4-P在胶州湾16个站位沉积物-海水界面上的交换速率。结果表明,PO_4-P的交换主要表现为由沉积物向水体的释放,其交换速率一般在 0.1～90 μmol·m~(-2)·d~(-1)范围内。根据 PO_4-P在不同类型沉积物-海水界面上的交换速率,估算出其在胶州湾海底沉积物-海水界面上的交换通量为 9.76×10~6mmol·d~(-1),仅占河流输入量的 24％,可提供浮游植物生长所需磷的 9％±3％。 相似文献
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土壤和沉积物中活性铁对有机质的吸附对有机质具有长期稳定和保存作用,从而在地质时间尺度上缓冲大气CO2浓度。本文利用连二亚硫酸钠还原性溶解提取活性铁氧化物（FeR）及与之结合的有机碳（Fe-OC）,定量研究了南黄海沉积物中FeR与OC之间的结合方式以及FeR对OC的保存作用,讨论了深度增加对二者相互作用的影响。结果表明,南黄海沉积物中Fe-OC占沉积物总有机碳的份数（fFe-OC）为（13.2±7.47）%,即活性铁对OC的年吸附量为0.72 Mt,占全球边缘海沉积物TOC年埋藏通量的0.44%。Fe-OC的平均OC:Fe为4.50±2.61,表明共沉淀作用对有机质的保存起重要作用,且其比值随海源有机质含量增加而增加。Fe-OC稳定碳同位素（δ13CFe-OC）结果表明,FeR优先保存活性有机质,但这种选择性随OC:Fe增大而减弱。随深度增加,fFe-OC和δ13CFe-OC均未表现出显著变化,这与该海域沉积物中有机质活性较低、铁还原作用较弱有关。 相似文献
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H. Elderfield 《Marine Chemistry》1976,4(2):103-132
Application of a simple model describing regional variations in the contents of manganese and associated minor metals in deep-sea sediments suggests that solid manganese phases are being removed from the <0.5 μm fraction of seawater at ～1–7 · 1012g yr?1 in excess of the rate of stream-supplied manganese. This flux is consistent with: (1) the relative rates of sediment accumulation in the Atlantic and Pacific Oceans; (2) the contrast between the oceanic residence time of manganese calculated from stream-supply data (14 · 103 yr) and from the flux of manganese precipitating in marine sediments or as manganese nodules (0.38–2.4 · 103 yr); (3) the surplus mass of manganese revealed by geochemical balance calculations (22.9 · 102g). On this basis excess manganese is accumulating in deep-sea sediments at 0.2–2.0 · 10?6 g cm?2yr?1. Manganese supplied to the upper layers of marine sediments by diagenesis has been evaluated with the aid of vertical advection—diffusion—reaction models. The calculated diagenetic flux of manganese at the sediment surface in a near-shore environment is in agreement with the known accretion rate of manganese deposits (1.7 · 10?2 g cm?2 10?3 yr?1) and the regionally variable flux over the area assessed is consistent with the presence or absence of manganese nodules at or near the water-sediment interface. The diagenetic flux at the surface of deep-sea sediments has been calculated at 0.7 · 10?4 g cm?2 10?3 yr?1 when the upper, oxic, zone of the sediment is ～20 cm thick. A limiting factor on the in situ production flux of dissolved manganese in deep-sea sediments appears to be the availability of reducing agents for manganese dissolution rather than the rate of downward transport of manganese-rich sediment to a reaction boundary where dissolution takes place. Various estimates of the rate of upward-migrating manganese suggest that manganese precipitates in the oxic zone with a rate constant of ～10?7 sec?1 with the result that diagenetic processes cannot supply the flux of excess manganese through more than ～0.25 m of oxic sediment. However, estimates of the flux of manganese to the oceans by submarine volcanic processes (0.79–1.1 · 1012g yr?1) are similar to the surplus mass of manganese detected by geochemical balance calculations (0.7 · 1012g yr?1). If submarine hydrothermal solutions provide only 10% of this excess then their computed discharge rate (39 g cm?2 yr?1) and residence time in the upper layer of oceanic crust (130,000 yr) agree well with these parameters for continental thermal springs. 相似文献
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Selenium in sediments, pore waters and benthic infauna of Lake Macquarie, New South Wales, Australia 总被引：1，自引：0，他引：1
G. M. Peters W. A. Maher F. Krikowa A. C. Roach H. K. Jeswani J. P. Barford V. G. Gomes D. D. Reible 《Marine environmental research》1999,47(5):2518
Measurements of selenium in sediments and benthic infauna of Lake Macquarie, an estuary on the east coast of Australia, indicate that sediments are a significant source of selenium in the lake's food web. Analysis of surficial sediment samples indicated higher selenium concentrations near what are believed to be the main industrial sources of selenium to the lake: a smelter and a power station. Sediment cores taken from sediments in Mannering Bay, near a power station at Vales Point, contained an average of 12 times more selenium in surficial sections than sediment cores from Nord's Wharf, a part of the lake remote from direct inputs of selenium. The highest selenium concentration found in Mannering Bay sediments (17.2 μg/g) was 69 times the apparent background concentration at Nord's Wharf (0.25 μg/g). Pore water concentrations in Mannering Bay were also high, up to 5 μg/l compared to those at Nord's Wharf which were below detection limits (0.2 μg/l). Selenium concentrations in muscle tissues of three benthic-feeding fish species (Mugil cephalus, Platycephalus fuscus, Acanthopagrus australis) were significantly correlated (p<0.05) with surficial sediment selenium concentration. Selenium concentrations in polychaetes and molluscs of Mannering Bay were up to 58 times higher than those from Nord's Wharf. Two benthic organisms, the eunicid polychaete Marphysa sanguinea and the bivalve mollusc Spisula trigonella, were maintained at different densities in selenium-spiked sediments. Both animals accumulated selenium from the spiked sediment, confirming that bioaccumulation from contaminated sediments occurs. Collectively, these data suggest that benthic food webs are important sources of selenium to the fish of Lake Macquarie. 相似文献
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Parke A. Rublee Susan M. Merkel Maria A. Faust 《Estuarine, Coastal and Shelf Science》1983,16(5):501-509
The number of bacteria in sediments, interstitial water and overlying tidal water of an oligohaline marsh system are about 109, 106 and 106 cells cm?3, respectively. Average cell size in the overlying water (about 0·06 μm3), is much smaller than that in sediments and interstitial water (about 0·18 μm3). Most bacterial cells in sediments are bound to sediment particles and less than 1% of the cells were displaced by percolating water through sediment columns. Concentration of bacteria in flooding tidal waters is generally higher than that in ebbing waters. Movement of bacterial biomass does not appear to be a significant mechanism of particulate organic transport in marsh sediments and marsh sediments do not appear to be a source of suspended bacteria for estuaries. 相似文献
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Keith A. Kvenvolden 《Marine and Petroleum Geology》1985,2(1):65-71
Two sites of the Deep Sea Drilling Project in contrasting geologic settings provide a basis for comparison of the geochemical conditions associated with marine gas hydrates in continental margin sediments. Site 533 is located at 3191 m water depth on a spit-like extension of the continental rise on a passive margin in the Atlantic Ocean. Site 568, at 2031 m water depth, is in upper slope sediment of an active accretionary margin in the Pacific Ocean. Both sites are characterized by high rates of sedimentation, and the organic carbon contents of these sediments generally exceed 0.5%. Anomalous seismic reflections that transgress sedimentary structures and parallel the seafloor, suggested the presence of gas hydrates at both sites, and, during coring, small samples of gas hydrate were recovered at subbottom depths of 238m (Site 533) and 404 m (Site 568). The principal gaseous components of the gas hydrates wer methane, ethane, and CO2. Residual methane in sediments at both sites usually exceeded 10 mll?1 of wet sediment. Carbon isotopic compositions of methane, CO2, and ΣCO2 followed parallel trends with depth, suggesting that methane formed mainly as a result of biological reduction of oxidized carbon. Salinity of pore waters decreased with depth, a likely result of gas hydrate formation. These geochemical characteristics define some of the conditions associated with the occurrence of gas hydrates formed by in situ processes in continental margin sediments. 相似文献
16.
Sedimentation rates were determined with the210Pb technique in six sediment cores from Harima Nada (Harima Sound), Seto Inland Sea. The rate of deposition varies from 0.11 g cm–2y–1 in the northern part to 0.33 g cm–2 y–1 in the southern part of the basin. A marked increase in copper and zinc content was observed above a depth in the core corresponding to about 1900 A.D. as a result of increasing human activities. Anthropogenic input of copper and zinc decreased slightly after 1970. Natural background levels of copper and zinc in the sediment in this sound are 11–16 ppm and 100–120 ppm, respectively. The total amounts of anthropogenic copper and zinc in the sediments were estimated to be 110–180g cm–2 and 610–1,280g cm–2, respectively. These values constitute 40–50% of the total sedimentary input of copper and zinc in the sediments since about 1900 A.D. 相似文献
17.
Bacterial iron oxide reduction in a terrigenous sediment-impacted tropical shallow marine carbonate system, north Jamaica 总被引：1，自引：0，他引：1
Kevin G. Taylor Christopher T. Perry Anthony M. Greenaway Philip G. Machent 《Marine Chemistry》2007,107(4):449-463
Discovery Bay, a carbonate-dominated embayment in north Jamaica, has been subject to inputs for 40 years of iron-rich bauxite sediment associated with the local mining and transport of processed bauxite. As such, this site is an ideal natural laboratory to study the records and impacts of iron oxide inputs upon geochemical, diagenetic, and microbial processes in tropical carbonate sediments.Total Fe contents in sites in the bay not receiving bauxite inputs are negligible and porewater Ca2+, SO42− and Cl− indicate that bacterial sulphate reduction is an important process. In contrast, surface sediments receiving bauxite inputs contain significant total Fe, from 44 μmol/g in shallow (5 m water depth) sites to 110 μmol/g in deeper (20 m water depth) sites. Up-core increases in total Fe record increased temporal inputs into the bay. Within these Fe-rich sediments porewater data shows the presence of FeII released by bacterial FeIII reduction. There is no direct evidence for significant bacterial sulphate reduction in these sediments. Iron oxides within all bauxite-impacted sediments display a high potential reducibility, from 40% to 80% of the total Fe present as dithionite-extractable FeIII. Experimental analysis of the potential susceptibility to, and rates of, bacterial FeIII reduction, utilising Discovery Bay sediment and Shewanella putrefaciens CN32 (a known FeIII-reducer) has confirmed the high bacterial reducibility of iron oxides within the sediment. Up to 75% of initial dithionite-extractable FeIII in the sediments was reduced over 15 days.The presence of iron oxides within the Discovery Bay shallow marine carbonate systems has markedly altered the chemical diagenetic processes taking place, with a shift from apparent dominance of bacterial sulphate reduction at non-impacted (Fe-poor) sites, to highly significant bacterial FeIII reduction in Fe-rich bauxite-impacted sediments. Given the perceived global increases in terrigenoclastic sediment inputs into tropical carbonate systems as a result of land-use and climate changes, coupled with the documented role that iron oxide reduction plays in nutrient and contaminant cycling in sediment systems, more research into the perturbation of early diagenesis by iron oxide inputs is required. 相似文献
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在2011年7月利用35SO2-4培养示踪法测定九龙江河口两个站位(A站位位于咸淡混合区,盐度3~5;B站位位于海相区,盐度20~25)沉积柱中硫酸盐还原速率的垂直分布。结果显示A站位沉积柱中硫酸盐还原速率变化范围为54~2 345nmol/(cm3·d),从表层到底部先增大后减小,最大值出现在20cm深度附近;B站位硫酸盐还原速率在24~987nmol/(cm3·d)之间,分别在10cm和78cm深度附近出现两个峰值,分别为876nmol/(cm3·d)和987nmol/(cm3·d)。综合分析两个站位孔隙水中SO2-4、甲烷浓度和沉积物中总有机碳、温度和氧化还原电位的垂直变化趋势与其硫酸盐还原速率的分布规律,表明A站位沉积物中硫酸盐还原以有机矿化为主;B站位受到有机质矿化和甲烷厌氧氧化的共同作用;两个站位硫酸盐还原速率及垂直分布趋势受孔隙水中SO2-4浓度、有机质活性和温度的共同影响;根据各个层位硫酸盐还原速率估算两个站位硫酸盐还原通量(以硫计)分别为527.9mmol/(m2·d)和357.1mmol/(m2·d),表明硫酸盐还原是九龙江河口有机质厌氧矿化的重要路径。 相似文献
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《Marine Chemistry》2001,73(2):125-152
We report here bioturbation and sediment accumulation rates determined from replicate sediment cores at four different sampling sites on the Palos Verdes shelf, Southern California, using bomb fallout and natural radionuclides (137Cs, 239,240Pu, 210Pb, 234Th, and 14C), along with supporting measurements of organic carbon (OC), porosity and granulometry. Present-day particle reworking, on time scales of several months, is restricted to the upper 3 cm, with rates ranging from 13 to 200 cm2/year, as deduced from 234Thxs profiles. There is little evidence that particle reworking reached depths significantly greater than 5 cm. Post-1963 (or post-1971) sediment accumulation rates ranged from 0.7 to 1.4 g/cm2/year (equivalent to 1.1–1.8 cm/year for surficial sediments), as calculated from Pu and Cs isotope profiles, with little change over time or distance from the outfall. Lateral transport of older sediment and multiple sediment sources on the Palos Verdes shelf is suggested from radiocarbon measurements on foraminifera and bulk sedimentary organic matter at two sampling sites, which showed variable, old and refractory sources of OC. Pre-1953 sediments accumulated at rates that were at least 0.4 g/cm2/year (≥0.3 cm/year), based on 210Pbxs dating. Given the abundance of sediment sources to the Palos Verdes shelf, the high sedimentation rates, and shallow particle mixed layers, contaminant-enriched layers should continue to move deeper into the sediments. 相似文献