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1.
微塑料与水中污染物的联合作用研究进展 总被引：1，自引：0，他引：1
微塑料(直径5mm的塑料)因其吸附、迁移性能和生物毒性成为目前研究的热点。微塑料进入水体后,会与水中的持久性污染物和重金属进行相互作用,与它们单独作用于生物的毒性效应不同。本文从微塑料对污染物的富集、迁移以及微塑料与污染物的联合毒性效应方面,对微塑料与污染物的联合作用进行了总结。环境中的微塑料能通过吸附作用富集水中有机污染物和金属离子,该过程主要受微塑料自身性质、塑料的老化程度、污染物的空间分布和其他环境条件的影响。污染物能以微塑料为载体在环境和生物体间迁移,包括空间上的转移和生物体内的转移。微塑料与污染物联合作用于生物体时,会通过增加摄入浓度、加剧组织损伤和降低机体抗性等方式增强污染物对生物体的毒性效应,或者通过降低污染物接触浓度、污染物或共污染物的生物可利用性减缓污染物对生物体的毒性效应。未来应对微塑料的吸附行为、相互作用机制以及评价方法、生物积累和慢性毒性进行探究。 相似文献
2.
自20世纪70年代人们就认识到,环境中重金属的浓度常常不能反映其生物可利用性和毒性,这些性质不仅取决于它们在环境中的浓度,而且还与其形态有关[1].在海水的溶解态金属中,通常认为自由水合离子对浮游植物具有较高的生物可利用性和毒性,而无机络合物和有机络合物的生物可利用性很小[2～4].在沉积物中,普遍认为可交换态的重金属最易被生物所利用,毒性最强,铁锰氧化物态可在还原条件下释放,而残渣态的重金属与沉积物的结合最牢固,活性最小,因而毒性最小[5].同种金属的不同赋存形态有着不同的生物可利用性,也就是说金属总的含量中只有一部分是具有生物可利用性的.因此在评价海洋环境中重金属的污染情况和制定相关标准时,必须考虑到重金属的赋存形态对生物可利用性和毒性的影响,以便更好的保护和管理海洋环境.海洋中的有机物质是痕量金属的重要配位体,这些金属-有机配位体影响着大部分生物可利用金属的化学形态[6].因此,作者在综述了海洋环境中重金属的赋存形态及生物可利用性的基础上,还详细讨论了有机物对海洋环境中重金属的赋存形态及生物可利用性的影响. 相似文献
3.
微塑料在海洋中的分布、生态效应及载体作用 总被引：2，自引：1，他引：1
微塑料通常被定义为最大尺寸小于5 mm的塑料碎片.受人类活动的影响,微塑料在海洋环境中广泛存在,引起了人们对其潜在影响的关注.由于粒径较小,微塑料可以通过多种途径进入水生生物体内,沿着食物链迁移、传递,影响海洋生态系统的健康与稳定.在海洋中长期停留的微塑料会吸附环境中的重金属、有机污染物和微生物等,加剧微塑料对海洋生物的毒性作用.本文综述了海洋环境中微塑料的污染特征,微塑料对海洋生物行为、生理等的影响,以及微塑料与微生物、其他污染物的相互作用和复合效应,并对微塑料对海洋环境及生物影响的研究进行了展望. 相似文献
4.
缺氧沉积物中硫化物对镉的生物可利用性的影响 总被引：2，自引：0，他引：2
镉是水环境中主要的金属污染物质,趋向于在沉积物中富集,对底栖生物造成潜在的威胁,并且通过食物链最终影响人体的健康.已经证明,作为沉积物中两大主要污染物的有机物和金属,有机碳是控制沉积物中非离子态有机化合物生物可利用性的主要因子[1],因此利用有机碳归一化方法判断沉积物是否受到有机物污染成为可能,而沉积物中金属的毒性或它的生物可利用性会受到诸如生物、物理和化学因子的影响,其中沉积物的部分化学组成会影响金属在固相与间隙水之间的分配,从而成为控制金属生物可利用性的关键因子[2,3]. 相似文献
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7.
重金属的存在形态与生态毒性 总被引：13，自引：0，他引：13
近年来,由于工业的发展,人类向环境中排放的重金属污染物日益增多,所有污染物的最终归宿是占地球表面积71％的海洋。这种污染已经直接或间接地对人类健康和各种生物造成了威胁。因此,海洋污染尤其是重金属污染的地球生物化学和生态毒理学吸引了众多的化学、生物、环境工作者的兴趣。近年来,关于重金属对生态环境的影响方面有许多工作,发表的文献已有数百篇,重金属形态与其生态毒性关系主要是从化学的角度出发,探索重金属 相似文献
8.
洋山港的建设及运营将会造成其所在的舟山海域受到重金属的污染,也会对其邻近的杭州湾造成一定程度的影响。
就舟山海域和杭州湾北岸的海水与生物体内的重金属含量进行了分析与评价,结果表明,在表层海水中,舟山海域Hg污染
最为严重,尤其是洋山港所在的小洋样点,其周边杭州湾北岸以Pb、Hg 为主要污染物。在生物体内,舟山海域中日本笠藤
壶、白脊管藤壶体内Hg超标情况最为严重,与该海域水体中Hg 的严重污染相对应;杭州湾北岸僧帽牡蛎体内Cu 超标情况
最为严重,大洋和小洋样点的僧帽牡蛎与两种藤壶体内重金属的污染程度和特性差异较大,这与物种不同而导致重金属进入
生物体内的分配机制差异有关,其体内Hg 含量与该海域表层海水Hg 含量呈极显著相关性,说明僧帽牡蛎可作为杭州湾北岸
Hg污染的指示生物。 相似文献
9.
环境中的污染物，极少单一存在，往往是多种并存。因此，它们对生物的影响是综合性的，可能产生拮抗(Antagonism)或协同作用(Synergism)。然而，以实验的方法研究多种重金属对海洋动物的效应的报道目前还不多见。已有的多为单种元素的实验研究，如Cunningham和Tripp，对汞在美洲牡蛎体内的积累、排出以及用同位素标记其在组织中的分布做了不少工作； Eisler等做了镉对海洋动物影响的研究；Phillipst近几年来做了监测重金属污染物的生物指标种的探讨。
毛蚶Arca (Anadara) subcrenata Lischke，在我国沿海均有分布，大量产于渤海，是沿海地区的重要食用贝类。作者以毛蚶为实验材料，探讨镉、铜、铅、镍、铬等五种混合的重金属在其体内的积累、排出和在器官组织中的分布，以及盐度变化对其积累的影响。这对于了解重金属对海洋生物的影响，进行环境质量的综合评价是很必要的，尤其在环境条件较为复杂的河口和海湾区域更具有重要意义。 相似文献
10.
通过深入分析海洋中碳、营养盐、微量金属元素的地球化学特性对酸化响应的研究进展,指出海洋酸化不仅会影响海洋中的碳化学,而且能影响海洋中营养盐、微量元素等的地球化学特性和过程;海洋酸化一个重要的、但被低估的结果是能大范围地改变海洋碳系统之外的无机和有机化学环境;不同海域的生物和地球化学系统对酸化产生不同的响应,同一物质循环的不同过程对酸化的响应可能截然不同;酸化给海洋带来的影响是极其复杂多变的,而且这些影响之间还存在错综复杂的相互作用;生态系统对海洋酸化的自然响应是很多生物和非生物因素独立和共同作用的结果,对很多单一物种或单一因素酸化响应的简单概括或总结,远不能描述海洋酸化对整个生态系统的影响规律。海洋酸化微量元素响应研究,应该具体到物质循环的关键环节(如碳泵、生物泵、硝化作用、固氮作用以及元素赋存形态转化等)及关键要素(如POM,DOM及CDOM等)等的响应,并探讨它们之间的相互作用,进而更全面地了解海洋酸化对海洋中物质循环的影响。 相似文献
11.
Dissolved Organic Matter in Oceanic Waters 总被引：13，自引：0，他引：13
The amount of information on oceanic dissolved organic matter (DOM) has increased dramatically in the last decade thanks to
the advances in chemical characterization. This information has supported the development of some novel and important ideas
for DOM dynamics in the ocean. Consequently, we have a better understanding of the importance of DOM in oceanic biogeochemical
cycles. Here we review studies published mainly during 1995–2001, synthesize them and discuss unsolved problems and future
challenges. The measurement, distribution and turnover of dissolved organic carbon (DOC) are presented as the bulk dynamics
of the oceanic DOM. The size spectrum, elemental composition, and chemical compositions at molecular and functional group
levels are described. The mechanisms proposed for the survival of biomolecules in DOM are discussed.
This revised version was published online in July 2006 with corrections to the Cover Date. 相似文献
12.
Bianchi TS Cook RL Perdue EM Kolic PE Green N Zhang Y Smith RW Kolker AS Ameen A King G Ojwang LM Schneider CL Normand AE Hetland R 《Marine environmental research》2011,72(5):248-257
Here we present results of an initial assessment of the impacts of a water diversion event on the concentrations and chemical composition of dissolved organic matter (DOM) and bacterioplankton community composition in Barataria Bay, Louisiana U.S.A, an important estuary within the Mississippi River Delta complex. Concentrations and spectral properties of DOM, as reflected by UV/visible absorbance and fluorescence, were strikingly similar at 26 sites sampled along transects near two western and two eastern areas of Barataria Bay in July and September 2010. In September 2010, dissolved organic carbon (DOC) was significantly higher (568.1-1043 μM C, x=755.6+/-117.7 μM C, n=14) than in July 2010 (249.1-577.1 μM C, x=383.7+/-98.31 μM C, n=14); conversely, Abs254 was consistently higher at every site in July (0.105-0.314) than in September (0.080-0.221), averaging 0.24±0.06 in July and 0.15±0.04 in September. Fluorescence data via the fluorescence index (FI450/500) revealed that only 30% (8 of 26) of the July samples had an FI450/500 above 1.36, compared to 96% (25 of 26) for the September samples. This indicates a more terrestrial origin for the July DOM. Bacterioplankton from eastern sites differed in composition from bacterioplankon in western sites in July. These differences appeared to result from reduced salinities caused by the freshwater diversion. Bacterioplankton communities in September differed from those in July, but no spatial structure was observed. Thus, the trends in bacterioplankton and DOM were likely due to changes in water masses (e.g., input of Mississippi River water in July and a return to estuarine waters in September). Discharge of water from the Davis Pond Freshwater Diversion (DPFD) through Barataria Bay may have partially mitigated some adverse effects of the oil spill, inasmuch as DOM is concerned. 相似文献
13.
Tracing dissolved organic matter in aquatic environments using a new approach to fluorescence spectroscopy 总被引：34，自引：0，他引：34
Dissolved organic matter (DOM) is a complex and poorly understood mixture of organic polymers that plays an influential role in aquatic ecosystems. In this study we have successfully characterised the fluorescent fraction of DOM in the catchment of a Danish estuary using fluorescence excitation–emission spectroscopy and parallel factor analysis (PARAFAC). PARAFAC aids the characterisation of fluorescent DOM by decomposing the fluorescence matrices into different independent fluorescent components. The results reveal that at least five different fluorescent DOM fractions present (in significant amounts) in the catchment and that the relative composition is dependent on the source (e.g. agricultural runoff, forest soil, aquatic production). Four different allochthonous fluorescent groups and one autochthonous fluorescent group were identified. The ability to trace the different fractions of the DOM pool using this relatively cheap and fast technique represents a significant advance within the fields of aquatic ecology and chemistry, and will prove to be useful for catchment management. 相似文献
14.
Seasonal variations in dissolved organic carbon concentrations and characteristics in a shallow coastal bay 总被引：8，自引：0，他引：8
Dissolved organic matter (DOM) composition and dynamics in temperate shallow coastal bays are not well described although these bays may be important as local sources of organic carbon to ocean waters and are often sites of economically-important fisheries and aquaculture. In this study surface water samples were collected on a monthly to bi-monthly basis over two years from a mid-Atlantic coastal bay (Chincoteague Bay, Virginia and Maryland, USA). Dissolved organic carbon (DOC) concentrations and light absorbance characteristics were measured on sterile-filtered water, and high-molecular weight (> 1 kDa) dissolved OM (DOM) was isolated to determine stable isotope composition and molecular-level characteristics. Our time series encompassed both a drought year (2002) and a year of above-average rainfall (2003). During the dry year, one of our sites developed a very intense bloom of the brown tide organism Aureococcus anophagefferens while during the wet year there were brown tide bloom events at both of our sampling sites. During early spring of the wet year, there were higher concentrations of > 1 kDa DOC; this fraction represented a larger proportion of overall DOC and appeared considerably more allochthonous. Based upon colored dissolved organic matter (CDOM) and high-molecular weight DOM analyses, the development of extensive phytoplankton blooms during our sampling period significantly altered the quality of the DOM. Throughout both years Chincoteague Bay had high DOC concentrations relative to values reported for the coastal ocean. This observation, in conjunction with the observed effects of phytoplankton blooms on DOM composition, indicates that Chincoteague Bay may be a significant local source of “recently-fixed” organic carbon to shelf waters. Estimating inputs of DOC from Chincoteague Bay to the Mid-Atlantic Bight suggests that shallow productive bays should be considered in studies of organic carbon on continental shelves. 相似文献
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16.
Shuchai Gan Verena B.Heuer Frauke Schmidt Lars W?rmer Kai-Uwe Hinrichs 《海洋学报(英文版)》2023,42(1):109-119
Marine sediments represent a major carbon reservoir on Earth. Dissolved organic matter(DOM) in pore waters accumulates products and intermediates of carbon cycling in sediments. The application of excitation-emission matrix spectroscopy(EEMs) in the analysis of subseafloor DOM samples is largely unexplored due to the redoxsensitive matrix of anoxic pore water. Therefore, this study aims to investigate the interference caused by the matrix on EEMs and propose a guideline to prepare pore water sam... 相似文献
17.
Dissolved organic matter (DOM) and dissolved copper-organic complexes were isolated from the estuarine waters of Narragansett Bay, RI, using reverse-phase liquid chromatography (RPLC). Different types of reverse-phase BOND ELUT columns (Analytichem International), including C2, C18 and phenyl-bonded phases, were studied to determine their adsorption efficiency for extracting DOM. Extraction efficiencies followed the order phenyl > C18 > C2, and phenyl − C18 > C2 for DOM and organic copper, respectively. However, comparisons of BOND ELUT and C18 SEP-PAK (Waters Associates) columns indicated that SEP-PAK columns were the most efficient when both DOM and organic copper were considered. Chromatographic profiles of the isolated DOM obtained using high-performance liquid chromatography were similar in elution characteristics and resembled chromatograms typical of fulvic acid. The UV-absorption characteristics of the DOM showed small differences and suggested that the different reverse-phase columns isolated material that was qualitatively similar.Copper-organic complexes isolated using C18 RPLC were studied to examine the dissociation of organically bound copper in seawater as the pH is lowered. Only a small amount of the complexed copper was displaced by the H+ with about 40% of the copper remaining bound at pH 3. However, the chromatographic elution behavior of the DOM and organic copper was significantly altered under acidic conditions as a result of protonation of acidic functional sites on the organic matter. 相似文献
18.
We performed a comprehensive metaproteomic analysis of the dissolved organic matter (DOM) in Japanese coastal waters using liquid chromatography–tandem mass spectrometry and demonstrated that these proteomes were characterized by proteins with various functions, including metabolic enzymes, membranes, and photosynthetic proteins. The protein sources included cyanobacteria, heterotrophic bacteria, and eukaryotic phytoplankton. Most of the components were similar among samples and also similar to pelagic components. We also observed differences in the compositions of the microbial communities of origin among the different dissolved protein samples and differences in the relative abundance of specific dissolved protein types (e.g., cytoskeletal proteins), possibly indicating potential dynamics in the coastal DOM pool. 相似文献
19.
《Deep Sea Research Part I: Oceanographic Research Papers》2001,48(1):49-62
Carbon overconsumption, i.e. the consumption of inorganic carbon relative to inorganic nitrogen in excess of the Redfield ratio at the sea surface, was examined in relation to the dynamics of dissolved organic carbon and nitrogen (DOC and DON) in the northeast Atlantic. We observed the presence of N-poor dissolved organic matter (DOM) in surface water during summer, requiring the consumption of inorganic carbon and nitrogen in a ratio exceeding the Redfield ratio. The C : N ratio of bulk DOM is not only different from the Redfield ratio but also variable, i.e. no fixed conversion factor of C and N exists where DOM is important in C and N transformations. The existence of N-poor DOM is recognized as a feature typical of oligotrophic systems. At the same time, the C : N ratios of particles conform to Redfield stoichiometry as does deep-ocean chemistry. The implications of this finding are discussed, the conclusion being that, while DOM buildup contributes to CO2 drawdown seasonally, its impact on long-term carbon and nitrogen balance of the ocean is small. 相似文献
20.
《Marine Chemistry》2001,73(3-4):253-271
The influence of mangrove-fringed tropical estuaries on coastal carbon budgets has been widely recognised. However, a quantitative differentiation between riverine and mangrove-derived inputs to the dissolved (DOM) and microparticulate organic matter (POM) pool of these environments has been hitherto not possible. Based on lignin-derived phenols and stable carbon isotopes a chemical signature for mangrove, terrestrial and marine-derived organic matter was established for a mangrove estuary in North Brazil. A mixing model was applied to calculate the contribution of each of the three sources to the DOM and POM pool in the estuary throughout 18 tidal cycles in the course of one year. Best source assignment for POM was reached with the yield of lignin phenols and δ13C as paired indicators, while the origin of DOM was best identified by the yield of lignin phenols and the acid to aldehyde ratio of vanillyl phenols. Although only about 6% of the fluvial catchment area is covered by mangroves, their contribution to the estuarine DOM and POM pool generally exceeded several times the terrigenic input from the hinterland. This outwelling of mangrove-derived organic matter was enhanced during the rainy season. DOM and POM were exported from the mangrove to the estuary in similar proportions. Most mangrove-POM was rapidly removed from the water column, while mangrove-DOM behaved conservatively. In contrast, terrestrial DOM was almost entirely removed in the outer part of the estuary, which was accompanied by a concomitant increase in terrestrial POM. This seems to be the result of a geochemical barrier zone for this type of DOM in the estuary. Generally, a high proportion of mangrove-DOM was present in the outer part of the estuary, even at high tide. This indicates DOM outwelling from mangroves in adjacent bays or estuaries and points to similar driving forces controlling this process on a regional scale. Mangroves probably play a more important role than rivers for marine carbon budgets along the North Brazilian coast south of the Amazon estuary. 相似文献