近海环境地球化学调查研究历史与现状   总被引：1，自引：0，他引：1  

叶思源  周永青  刘兆茂  刘建霞 《海洋地质与第四纪地质》2003,23(4):121-126

近海环境地球化学的研究是一支新兴的发展中的边缘性分支学科，由于环境问题的日益突出，该学科发展较为迅速。通过回顾我国近海环境地球化学调查的历史和综述当今国外该学科的研究现状，概括了该学科的主要进展，并指出存在的问题和今后的发展方向。  相似文献   

Budgets of Mn,Cd and Cu in the macrotidal Gironde estuary (SW France)     

Stéphane Audry  Gérard BlancJörg Schäfer  Frédéric GuérinMatthieu Masson  Sébastien Robert 《Marine Chemistry》2007

The behavior and budget of Mn, Cd and Cu in the Gironde estuary were investigated through data from both the water column (WC) and sediment depth profiles. In the estuarine freshwater reaches, Mn and Cd removal from and Cu addition to the dissolved phase occurs with a magnitude equivalent to 10%, 30% and 25% of their respective annual fluvial gross dissolved input, respectively. In the saline estuary, diffusive benthic outflow is the main source of dissolved Mn (74% of the total gross dissolved input within the estuary) to the WC. In contrast, Cd (96%) and Cu (89%) are mainly released into the dissolved phase of the WC from fluvial, estuarine and dredging-related particles through complexation (Cd) and organic carbon mineralization (Cu). Anthropogenic activities (sediment dredging) induce pore water inputs, particulate sulfide oxidation and sediment resuspension, significantly contributing to the metal budget of the WC. The related amounts of metals released could be equivalent to 20–50% (Cd) and up to 70% (Cu) of their respective net dissolved addition. Mass balances suggest that a large part of the metals previously released into the dissolved phase from processes within the estuary are removed by suspended particles due to (co-)precipitation of Fe/Mn (oxy)hydroxides and scavenging on autochthonous organic matter. On an annual basis, the Gironde estuary acts as a net sink of dissolved Mn, removing 60% of the dissolved fluvial inputs, and as a net source of dissolved Cd and Cu, contributing ∼ 85% and 20–45% to the dissolved Cd and Cu fluxes to the ocean.  相似文献   

西江河口重金属迁移扩散数值模拟的研究     

黄小平  唐永銮 《热带海洋学报》1992,(4)

本文以水体中重金属(包括溶解态和颗粒态)的物理迁移过程为基础,建立重金属迁移扩散的数学模式。模式中考虑悬浮物沉降和再悬浮对水体中重金属浓度的影响,并考虑咸潮活动引起悬浮物的絮凝沉淀作用。计算结果表明,这种潮汐河口区重金属迁移扩散模式基本上是成功的。并以镉为例,说明重金属在西江河口区迁移扩散的特点。  相似文献   

中国多金属结核开辟区间隙水中铜、锰、镍的分布规律   总被引：2，自引：1，他引：2       下载免费PDF全文

倪建宇  GRUPEBern  MAGGIULLIMichael  周怀阳 《海洋学报》2003,25(2):42-47

通过对东北太平洋海域中国多金属结核开辟区沉积物间隙水中铜、锰、镍等微量元素的详细研究表明,锰主要受沉积环境的影响,其含量的变化范围在0.16～8.61μg/dm3之间;铜和镍则主要与表层海水的初级生产力有关,研究区内间隙水中铜和镍含量的变化范围分别为0.16～20.8和0.80～3.12μg/dm3,且这些元素在沉积物—水界面处均存在最大浓度梯度.利用“Fick扩散定律”计算表明,锰在研究区主要是从上覆海水向沉积物扩散,是沉积物中锰的主要来源之一;而铜和镍则是从沉积物向上覆海水扩散,是底层海水中铜和镍的主要来源。与表层海水中铜和镍向底层海水的输送通量计算结果相比,底层海水中铜和镍的含量主要受沉积物的控制.  相似文献   

南海东部海域柱样沉积物浊流沉积探讨     

章伟艳  张富元  张霄宇 《热带海洋学报》2003,22(3):36-43

利用1998年南海东部陆坡69号柱样、深海盆149号柱样、南部岛礁323号柱样沉积物的粒度、化学、古生物、矿物等鉴定分析测试资料,分析了南海东部海域发生浊流沉积的地质背景、产生浊流沉积的条件和诱发因素,进而发现南海东部浊流沉积发育,在南北陆坡及中部深海盆地均有浊流沉积层。从其出现层位看,为氧同位素2—4期,即晚更新世中晚期。从浊流沉积出现层数分析,具有自北向南浊流发生频次减弱的趋势。从浊流沉积物成分看,南海东部浊流沉积物具有多样性,北部陆坡以陆源为主,中部深海盆以陆源及火山源为主,南部岛礁以生物源为主。  相似文献   

Spatial and seasonal variations in depth profile of trace metals in saltmarsh sediments from Sapelo Island, Georgia, USA   总被引：1，自引：0，他引：1  

Alakendra N. Roychoudhury   《Estuarine, Coastal and Shelf Science》2007,72(4):675-689

This study was undertaken to elucidate the impact of early diagenetic processes on the accumulation of trace metals in Sapelo Island saltmarsh sediments as a function of time, space and sediment properties. Samples were collected from three sites in summer (May 1997) and winter (January 1998) along a transect from an unvegetated Creek Bank through a vegetated Tidal Levee to the vegetated midmarsh with evident lateral heterogeneity caused by hydrologic regime, macrophytes and microbial and macrofaunal activities. A suite of trace metals (As, Ba, Cr, Co, Cu, Cd, Mo, Ni, Pb, Th, Ti, U, V, Zn and Zr) was analyzed to obtain their depth-distribution at the three sites. Spatially marked differences were observed, that were primarily related to hydraulic flushing of trace metals away from the sites in high-energy regimes, rapid downward mixing and reworking of sediment via bioturbation, and below-ground degradation and production of Spartina biomass. Although sulfate reduction and the formation of acid volatile sulfide and pyrite were dominant processes throughout the marsh, the trace metal scavenging role of sulfides was not apparent. However, possible sulfurization of organic matter, leading to enhanced trapping of trace metals with organic carbon, may have played an important role in sequestration of trace metals.No similarity was observed visually between the depth trends of trace metals and sediment properties (grain size, iron-oxyhydroxide content, acid volatile sulfides and pyrite content) that are known to play a major role in trace metal partitioning. Only organic carbon content closely followed the trace metal profiles at all the three sites. Minor variation in depth-integrated sediment trace metal content was observed seasonally at each of the three sites. Furthermore, the depth trend of profiles of individual trace metals also did not vary significantly over the seasons either.  相似文献   

Size distribution of colloidal trace metals and organic carbon during a coastal bloom in the Baltic Sea   总被引：1，自引：0，他引：1  

Johan Ingri  Susanna Nordling  Jenny Larsson  Jenny Rnnegrd  Nina Nilsson  Ilia Rodushkin  Ralf Dahlqvist  Per Andersson   rjan Gustafsson 《Marine Chemistry》2004,91(1-4):117-130

The physico-chemical speciation of organic carbon and selected metals was measured during a coastal bloom in Ekhagen Bay, Baltic Sea, using ultrafiltration.One important objective with the study was to see if any depletion of trace metals could be measured in the directly bioavailable fraction (<1000 Da, the soluble low molecular weight fraction, LMW) during a plankton bloom. Filters with five different cut-offs were used (1 kD (1000 Da), 5 kD, 10 kD, 100 kD and 0.22 μm) in order to delineate the size distribution of colloidal organic carbon (COC) and trace metals.During the bloom in May, LMW Al, Co, Cu, Mn and Ni concentrations decreased although the colloidal and particulate concentrations were relatively high. Data show that desorption of colloidal and particulate bound trace metals to the LMW fraction was slower than the process depleting the LMW fraction.Estimates of the maximum active uptake of Cu, Ni and Mn by the phytoplankton, and the loss of non-bioactive Al from the LMW fraction, indicate that processes other than active uptake by phytoplankton must contribute to the observed depletion of trace metals in the LMW fraction. Hence, in order to estimate the bioavailable pool of trace metals for plankton during bloom conditions, these other processes must be understood and quantified.Transparent Exopolymeric Particles (TEP, reflecting sugar-rich phytoplankton exudates) increased around eight times during the plankton bloom. We hypothesize that the formation of TEP is a process that might be important for the transfer of trace metals from the LMW to the particulate fraction during the phytoplankton bloom, but the significance of TEP for this depletion in Baltic Sea surface water remains to be shown.  相似文献   

Geochemical and hydrodynamic constraints on the distribution of trace metal concentrations in the lagoon of Nouméa, New Caledonia   总被引：1，自引：0，他引：1  

Christophe Migon  Sylvain Ouillon  Xavier Mari  Emmanuel Nicolas 《Estuarine, Coastal and Shelf Science》2007,74(4):756

Seawater samples were collected in the lagoon of Nouméa (southwest New Caledonia) along two transects from eutrophic coastal bays to the oligotrophic barrier reef. Land-based emissions to the lagoon were measured with dissolved and particulate concentrations of chromium (Cr) and nickel (Ni), used as tracers of both terrigenous and industrial (Ni ore treatment) activities, as well as dissolved and particulate concentrations of zinc (Zn), used as a tracer of urban effluents. The spatial variability of metal concentrations was related to geochemical and hydrodynamic conditions, i.e., respectively: (1) natural and anthropogenic emission sources, and chemical processes occurring in the water column; and (2) water residence times. The parameter used to describe the residence time of water masses was the local e-flushing time, i.e. the time required for a tracer mass contained within a given station to be reduced by a factor 1/e. High metal concentrations were found in coastal areas (up to 9000 ng dissolved Ni L⁻¹), and steeply decreased with distance from the coast (down to 101 ng dissolved Ni L⁻¹ near the barrier reef) to reach levels similar to those found in remote Pacific waters, suggesting a rapid renewal of waters close to the barrier. Distributions of metals in the lagoon are controlled upstream by land-based emission sources and later chemical processes. Then hydrodynamics constrain metal distributions, as shown by the observed relationship between local e-flushing times and the spatial variability of metal concentrations. In addition, a change in the direction of prevailing winds yielded a decrease of dissolved metal concentrations at the same site by a factor of 2.5 (Cr and Ni) and 2.9 (Zn). It is suggested that the residence time is a key parameter in the control of elemental concentrations in the lagoon waters, as much as land-based emission sources.  相似文献   

ICES baseline survey of trace metals in European shelf waters   总被引：1，自引：0，他引：1  

Balls  P.; Cofino  W.; Schmidt  D.; Topping  G.; Wilson  S.; Yeats  P. 《ICES Journal of Marine Science》1993,50(4):435-444

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离子色谱分析在黄土和粉尘研究中的应用   总被引：1，自引：0，他引：1  

王丹  屈文军  张小曳  严立文  曹国良 《海洋地质与第四纪地质》2005,25(1):113-118

黄土中存在着大量的碱金属及碱土金属，以往的测试方法多为原子吸收和ICP—MS，离子色谱法在测试黄土样品的碱金属和碱土金属元素含量中应用不多。将黄土地质标准样品进行消解后用离子色谱进行测试，测试效果良好，重复测试的相对标准偏差小于5％，与推荐值的相对误差小于5％，准确度和精密度符舍相关的质量控制要求。本实验方法测试的离子含量都在仪器响应呈线性的最佳测试范围之内，标准曲线经回归后相关系数均达到0．9999。黄土样品的分析结果与粉尘气溶胶样品的离子分析结果对比表明，此方法对于探讨粉尘起源以及沙尘暴天气的研究具有重要意义。  相似文献