珠江口外内陆架表层沉积物重金属元素形态特征、控制因素及生态风险分析

2011年对珠江口外内陆架海域22个点位表层沉积物中主要的重金属Cr、Ni、Cu、Pb、Zn、Cd和As含量、形态特征、来源控制因素以及潜在生态风险进行了研究。采用了BCR提取法分析各种重金属赋存形态,并依据各种重金属的形态特征与沉积物基质属性进行了相关因子分析,了解其分布的控制因素。结果表明:珠江口外内陆架沉积物重金属分布特征为由陆向海的方向,随着水深增大而逐渐降低。重金属赋存形态中Cr、Ni、Cu、As主要以残渣态存在,Pb主要以可还原态存在,Cd主要以酸提取态存在,Zn主要存在于残渣态与可还原态。各重金属非残渣态比重Cd最高,Cr最低,表明Cd的迁移性最强。各元素非残渣态在平面上的分布与总量分布模式相关性较好,因此,珠江口外内陆架海域通过总量来确定区域重金属污染情况在一定程度上是可靠的。重金属元素与黏土含量、可还原态Fe、Mn含量普遍具有较好的相关性。珠江口外内陆架的重金属来源比较复杂,主要来源于附近大陆的物质输入。运用酸提取态百分含量风险评估法对重金属潜在生态风险进行评价,发现研究区各元素综合风险评价除Cd为高风险外,Cr元素综合风险评价为无风险;其余为中一低风险等级。     

渤海中部表层沉积物中重金属赋存相态及来源

近年来由于环渤海经济圈的快速发展,渤海接受了来自周边河流、沿岸排污及海上油气开采所产生的大量的重金属等污染物质,使得渤海的生态环境系统面临前所未有的压力。本文采用电感耦合等离子质谱仪（ICP-MS）对采自渤海中部的25个表层沉积物样品中的Cu、Co、Ni、Zn、Pb、Cr、Cd等重金属元素的含量和赋存相态进行了分析,探讨了重金属分布规律、污染状况及来源。研究结果表明,Cu、Co、Ni、Zn、Cr在渤海湾的近岸区域和渤海中部泥质区有较高的含量,而Pb和Cd则在整个研究区的含量都较高;表层沉积物中Cu、Co、Ni、Zn、Cr主要以残渣态形式存在,而Pb和Cd则具有较高的非残渣态含量;生态风险评价结果表明该区表层沉积物未受到Co、Ni、Cr的污染,Cu、Zn、Pb和Cd则为未污染-中等程度污染。重金属元素Co、Ni、Cr以自然来源为主,在沉积物中的分布主要受沉积物物质组成的影响,而Cu、Zn、Pb,尤其是Cd,则受到了人类活动的显著影响。黄河沉积物是研究区表层沉积物中重金属的主要来源,影响范围涵盖了本区大部分区域,但在研究区的北端受到滦河来源物质的影响,渤海湾和研究区中部则受到海河物质和大气沉降来源重金属的一定影响。     

海水养殖池沉积物中重金属形态和生物酶活性的关系研究

以连云港市对虾养殖池表层沉积物为研究对象,采用Tessier连续萃取法,研究了表层沉积物中重金属(Cu、Zn、Pb、Cd、Cr、As、Mn)的赋存形态和酶(脲酶、碱性磷酸酶、过氧化氢酶、转化酶)活性的相关性。结果表明,重金属Cu和Zn以有机-硫化物结合态为主要的赋存形态,Pb以铁锰氧化物态为主要的赋存形态,Cd以可交换态(平均33.47%)和碳酸盐结合态(平均31.16%)为主要存在形态,Cr和As主要以残渣态存在,Mn的铁锰氧化物态比例最高。脲酶的活性范围为0.45—8.96mg/(g·24h),碱性磷酸酶活性范围为2.45—6.69mg/(g·24h),过氧化氢酶活性范围为0.14—2.36m L/(g·min),转化酶活性范围为0.45—10.45mg/(g·24h)。脲酶活性与Cd、As的可交换态、Cd的碳酸盐结合态、Cu、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态之间显著相关;碱性磷酸酶活性与Zn、Cd的铁锰氧化物态显著相关;过氧化氢酶活性与Cd的可交换态、碳酸盐结合态及残渣态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫结合态之间显著相关;转化酶活性与Cu、Cd、As的可交换态、Cd的碳酸盐结合态、Cu、Cd、As的铁锰氧化物态、Zn、Pb、Cd、Mn的有机硫化物态、Cd、As的残渣态之间显著相关。酶活性可以用来指示海水养殖池沉积物中重金属的形态转化过程。     

湄洲湾海域表层沉积物重金属含量的分布特征及潜在生态风险评价

根据2012年福建湄洲湾海域表层沉积物样品测定的7种重金属（Cr、Co、Ni、Cu、Zn、As、Pb）含量数据,研究重金属在沉积物中的含量和空间分布特征,然后运用主成分分析法分析各重金属的主要来源,最后采用潜在生态危害指数法评价其污染程度和潜在生态危害.结果表明,相对第一类海洋沉积物标准,Cu、Zn、As和Pb含量均未超标,Cr超标21.2%.大部分重金属含量平面分布总体呈现东北往西南递减的趋势,体现陆源输入的影响,As、Zn及Pb在7号站位、Cu在8号站位出现高值区可能更多地联系于研究区域本身的背景特征.Cr、Co、Ni和Zn含量之间相关性显著,且Co、As和Zn含量也两两表现出显著正相关.主成分分析表明岩石的自然风化和侵蚀是Cr、Co、Ni、Cu、Zn和As元素在研究区域表层沉积物的主要来源,Pb可能更多来源于海上交通航运和海水养殖.研究区域综合潜在生态危害为中等生态危害程度.     

珠江口荷包岛近岸海域沉积物重金属分布及其潜在生态危害评价

本文采用2008年在珠江口荷包岛近岸海域的调查数据,对表层沉积物重金属的分布特征及重金属与TOC的相关性进行了分析,并采用Hakanson潜在生态危害指数法对其生态危害程度进行了评价。结果表明:重金属Cd,Hg,Cr和As四种元素分布基本呈现荷包岛近岸海域较高的特点,重金属Zn,Pb和Cu的分布没有明显规律;重金属富集顺序为Cd＞Zn＞Cu＞Hg＞As＞Cr＞Pb。相关性研究表明,重金属Cu与Zn显著相关,Hg,Cr,Cd和As极显著相关;有机质是影响沉积物重金属迁移和转化的重要因素。潜在生态危害评价结果表明,荷包岛近岸海域表层沉积物重金属总体潜在生态危害轻微;各重金属生态危害程度顺序为Cd＞Hg＞As＞Pb＞Cu＞Cr＞Zn;对荷包岛近岸海域生态环境具有潜在生态危害的重金属主要是Cd和Hg。     

三沙湾表层沉积物重金属含量分布及生态风险评估

研究了三沙湾沉积物重金属的分布和污染情况,分别使用了主成分分析(PCA)、富集因子分析和潜在生态风险指数法对研究区域沉积物中重金属的来源、富集水平和生态风险这3个方面进行了探讨.主成分分析的分析将调查海域沉积物中金属元素分为自然来源和人为来源2类.其中Cu、Pb、Zn、Cd、Cr、Hg、As和Ni均为人为来源,该来源可能与沿岸的人类活动有关.富集因子法的分析结果表明,研究区域As、Ni、Cd、Cr、Pb、Cu、Zn、Hg处于低富集状态.这说明该地区由工业活动所导致重金属污染还处于初级阶段,其污染状况的发展需要及时关注.潜在生态风险指数法分析结果表明,研究区域80%站位(1、2、3、4、5、6、7、9、10、11、12和14)处于中等污染的生态风险水平,沉积物中Hg、Cd、As和Ni为主要生态危害的重金属元素.     

胶州湾滨海湿地盐渍土壤中重金属的聚集与分散特性研究

以胶州湾东北沿岸盐渍土壤为主要研究对象,分析探讨了滨海盐渍土壤对10种微量重金属的聚集／分散特征。结果表明,胶州湾东北沿岸盐渍土壤中Cu、Zn、Pb、Cd、As、Cr、Co、Ni、V、Mo主要来源于成土母质花岗岩的风化产物,Cu、Zn、Cr、Cd、Pb、Ni为“盐渍土壤聚集元素”,As、Co、V、Mo为“盐渍土壤分散元...     

烟台近岸典型生态区沉积物重金属形态分布及其污染状况

运用Tessier连续提取法,对烟台海岸带3个典型生态敏感区表层沉积物重金属Cr、Cu、Cd、Pb、Zn、Ni的形态分布和污染状况进行了分析研究。结果表明,研究区域中河口区与排污口区重金属Cr、Cu、Cd、Zn和Ni的含量较高,尤其是Cd污染严重。养殖区基本符合海洋沉积物质量第1类标准;重金属Cr、Cu、Pb、Zn和N...     

连云港临洪河口水体中重金属的化学形态与分布特征研究

对连云港海域临洪河口水体中重金属元素Cu,Zn,Pb,Cd的主要存在形态及悬浮颗粒态重金属元素的赋存形态进行了分析。结果表明:悬浮态重金属Cu,Zn,Pb,Cd的含量在调查海域内空间分布基本均衡,Zn、Cu、Cd主要以溶解态形式存在,而Pb则主要以颗粒态形式存在。对悬浮态重金属元素的赋存形态分析表明,Cu主要富集在有机-硫化物态、Zn主要富集在残渣态、Pb主要富集在铁锰氧化物态和碳酸盐结合态、Cd主要富集在可交换态和碳酸盐结合态。     

近10年三门湾海域表层沉积物重金属含量变化及来源解析

为了解三门湾海域表层沉积物重金属的含量和分布特征，本研究对三门湾海域2019年82个站位海域表层沉积物中的Cu、Pb、Zn、Cd、Cr、As及Hg共7种重金属元素的含量进行测定，并对比10年前的数据，分析了元素含量的变化情况，追溯了其主要物质来源。结果表明，三门湾海域表层沉积物中Cu、Zn、Pb、Cd、Cr、As、Hg的平均质量浓度分别是31.33、96.46、29.86、0.116、91.54、13.09、0.06 mg/kg,Cu、Cr的含量相对较高。与2009年相比，2019年三门湾海域表层沉积物Cu、Zn与Cd的含量大体上保持一致，Pb、Cr与As的含量有所上升，Hg的含量显著降低。沉积物重金属含量由近岸向外海依次降低，高值区主要集中在蛇蟠水道口、力洋港与健跳镇附近。运用主成分分析与因子分析对重金属物质来源进行解析的结果表明，重金属物质的来源与人类活动的影响密切相关。     

Size-fractionated uranium isotopes in surface waters in the Jiulong Estuary in China

Surface water was collected from the Jiulong Estuary for determination of activity concentrations of uranium isotopes in different size fractions, namely, greater than 53, 10 -53, 2 - 10, 0.4 -2 μm, 10 000 u -0.4 μm and less than 10 000 u fractions by microfihration and cross-flow uhrafiltration technologies. Results indicated that most of the dissolved uranium （ 〈 0.4 μm） exis- ted in the low molecular mass fraction （ 〈 10 000 u）, and the colloidal uranium-238 （10 000 u -0.4 μm） only contributed less than 1% of the dissolved uranium-238. The fractions of colloidal uranium in the dissolved phases decreased with the increasing sa- linity. A positive linear relationship between uranium-238 activities and salinities was observed for the dissolved, colloidal and low molecular mass fractions, indicating a conservative behavior of uranium in the Jiulong Estuary. In the particulate phases （ 〉 0.4 μm）, the partitioning of uranium isotopes among different size fractions was controlled by the partitioning of particle concentrations. In the regions with salinities below 20, the partitioning of uranium-238 among different size fractions was as follows： 10 - 53 μm 〉 2 - 10 μm 〉 0.4 - 2 μm greater than above 53 μm. However, the order at the offshore station with salinities above 30 changed as follows ： 0.4 - 2 μm 〉 10 - 53 μm 〉 2 - 10 μm greater than above 53 μm. The fraction of the 0.4 - 2 μm particles increased at the offshore station, suggesting the increased contribution of the authigenic uranium. The activity ratio of uranium-234 to uranium-238 in the dissolved phases, including the low molecular mass fraction and the colloidal fraction, was larger than unity, showing the occurrence of excess uranium-234. In contrast, the activity ratio of uranium-234 to uranium-238 in all size fractions of the particulate phase was close to the equilibrium value （1.0）. The observed different values of the activity ratio of uranium-234 to uranium-238 in the dissolved phase and the partic     

Recent progress in submarine geosciences in China

In China submarine geosciences represents a newly established discipline of oceanography, focusing on the oceanic lithosphere, and its interface with the hydrosphere and biosphere. Recently, supported by the National High Technology Research and Development Program and other high-tech development projects, significant progress has been made in the development of advanced technologies and equipment. This en- ables the scientists in China to carry out explorations of the international seabed area in the Pacific Ocean and on the Southwest Indian Ridge. In addition, they have been active in the research activities associated the mid-ocean ridges and western Pacific marginal seas. It is anticipated that this research field will continue to be highly fruitful in the near future.     

湄洲湾夏季的初级生产力

湄洲湾１９９２年夏季的叶绿素ａ，三磷酸腺苷，碳比积累速率，初级生产力的变化范围和均值分别为０．４５－４．７２，１．４９ｍｇ／ｍ＾３；０．１２－１．０７，０．３１μｇ／ｄｍ＾３；０．０６－０．５８，０．３４ｄ＾－１；０．０７－０．３４，０．２１ｍ／（ｍ＾２．ｄ）。叶绿素ａ与三磷酸腺苷之间。初级生产力与碳比积累速率之间均呈正相关关系。叶绿素ａ三磷本能腺苷的比值为４．８，湄洲湾夏季浮游植物的生长受氮不足     

夏季珠江口沉积物中营养盐剖面分布和界面交换通量

通过对夏季珠江口区域沉积物间隙水营养盐剖面分析,调查了营养盐含量分布和特征,探讨了有机物的降解特性、营养盐的底部通量估算和作用.结果表明,珠江口沉积物间隙水中营养盐以高含量铵盐为主要的存在形式,沉积物中有机物的降解反应主要在厌氧状态下进行,底部水体铵盐的增加来源于底部沉积物有机质的降解释放,而且对水体的营养盐循环有较大的贡献.     

Recent advances in marine technology in Canada

Much of the recent Canadian activity in marine technology has focused on development of capabilities in Arctic waters, and on the update and replacement of naval vessels. This paper describes some of the significant projects and programs now under way, and suggests future research and development requirements.     

一氧化氮在浮游植物中的研究进展

对一氧化氮在浮游植物中的研究进展进行了归纳,总结了一氧化氮对浮游植物生长的影响,探讨了浮游植物中一氧化氮的产生机制,并对今后的研究重点提出展望。     

Challenges in cross-sectoral marine protection in Europe

Marine environment protection in Europe faces a number of challenges. One is the coordination of relevant sectoral policies — such as agricultural and fisheries policies — with regard to marine protection objectives. The question in the following is on how marine protection issues can be more closely integrated in sectoral policies under the conditions prevailing at present. In particular the strength and weaknesses of the Marine Strategy Framework Directive (MSFD) as the key instrument for marine environment protection in Europe are analyzed in this context. In particular, the MSFD does not adequately address all sectors and policies which are relevant to marine environment protection. One possible means of giving the MSFD greater influences on other policies of relevance to marine waters is to integrate the objectives established under the MSFD in the European maritime policy. The aim should be to require the further development of sectoral policies to take unrestricted account of the objectives of the MSFD implementation process. But also other instruments of marine policy such as maritime spatial planning and marine protected areas are crucial to advance the protection of European seas.     

Seasonality in nutrient concentrations in Galveston Bay

In order to investigate factors controlling nutrient cycling in the shallow and turbid coastal ecosystem of Galveston Bay, data from: (1) the Texas Water Commission (TWC) database 1980–1989, and (2) salinity transects in 1989 and 1993 are presented and analyzed. Statistical regression and time-series analysis were carried out on data acquired by TWC between 1980 and 1989, in an attempt to establish seasonally of nutrient and chlorophyll-a (chl.-a.) concentrations in the bay and to determine factors which regulate these concentrations.A strong seasonality was found for phosphorus and chl.-a. in the upper and mid-bay stations. A recurring maximum for phosphate occurred in September and a chl.-a. maximum occurred regularly in March–April. It is hypothesized that benthic regeneration of phosphorus at the end of summer is responsible for the phosphate maximum. The inverse correlation of the partition coefficient (K_d) for phosphate with the concentration of suspended particulate matter (SPM), coupled to a strong enrichment of phosphate in suspended particles at low SPM concentrations, indicates additional control by geochemical and physical processes such as particle sorting and/or particle-colloid interactions. Nitrate is inversely correlated with salinity at the upper and mid-bay stations, indicating the Trinity River is a major source.Nutrient concentrations in the lower bay (East and West Bay stations) are considerably lower and less predictable, as they are not correlated with salinity or temperature. Data from the 1989 and 1993 transects confirm the yearly maximum in phosphate concentration in late summer months, with peak concentrations in the upper Trinity Bay. It is concluded that despite possible phosphate buffering by physical and geochemical mechanisms, relatively large concentration maxima recur regularly every year during the summer, possibly caused by a benthic source of phosphate.