鸭绿江口溶解态铝的行为

讨论１９９６ 年５ 月枯水期鸭绿江口溶解态铝的含量及其分布特征。结果表明,鸭绿江口溶解态铝的含量介于０．８１ ～３ ．５６μｍｏｌ／Ｌ之间;在河海混合初期铝快速清除,其后则表现为与低浓度海水的简单混合。并认为河口中悬浮颗粒物的吸附解吸作用与胶态和有机结合态铝的絮凝是造成鸭绿江口水体中铝清除的主要原因。     

九龙江河口区稀土元素地球化学特征

用电感耦合等离子体质谱（ICP-MS）对2007年10月航次采集的九龙江河口区溶解态、悬浮颗粒态、沉积物样品中的稀土元素（REEs）进行了测定,对REEs的地球化学特征进行研究.结果表明,REEs在各相态中的含量范围如下：溶解态的为0.1 ng/dm^3（Eu）～1.96μg/dm^3（Ce）,悬浮颗粒态的为0.28（Tm）～142.83（Ce）mg/kg,沉积物的为0.25（Tm）～99.65（Ce）mg/kg;溶解态、悬浮颗粒态及沉积物中REEs球粒陨石标准化配分曲线均表现为负斜率型,九龙江河口为LREE相对HREE富集型河口.九龙江河口溶解态、悬浮颗粒态、沉积物三相态中REEs含量受流域土壤、地表径流等源区因素影响较大.Ce异常值在各相态中表现为负异常.     

海南万泉河、文昌/文教河河口溶解态铝的分布及季节差异

本文讨论了2006年12月冬季和2007年8月夏季海南省万泉河、文昌/文教河河流及河口溶解态铝的含量、分布及季节差异。结果发现,万泉河冬、夏两季河流及河口溶解态铝的平均含量分别为(156±127)和(157±97)nmol/L,季节差异不明显。文昌/文教河冬、夏两季河流及河口溶解态铝的平均含量分别为(242±156)和(222±66)nmol/L,冬季溶解态铝的平均含量略高于夏季。万泉河溶解态铝在河海混合初期表现为清除行为,而后表现为保守混合行为,而文昌/文教河则表现出明显的非保守混合行为,在中等盐度区域存在明显外源输入,原因可能是八门湾底沉积物再悬浮过程中释放的影响。部分河流上游采样点由于受到人为活动引起的污水排放的影响,溶解态铝含量明显增加。万泉河、文昌/文教河溶解态铝的平均含量明显低于我国其他及世界主要河流。     

胶体磷在河口IX随盐度变化的研究

研究了胶体磷在河口海区随盐度变化的趋势,并将其与颗粒态、真溶解态磷随盐度的变化趋势进行对比,分析胶体态磷在河口的行为与颗粒态磷和真溶解态磷二者的异同.探讨磷在颗粒相,胶体相和真溶液相之间的分配及其与悬浮颗粒物浓度的关系,研究胶体磷在河口海区中的迁移转化作用.研究结果表明,胶体相中总磷、有机磷和活性磷浓度由河端向海端降低,表明陆源输入是其主要来源.胶体有机磷占总磷比例随盐度增加而下降,表明有机磷受胶体去除过程的影响较明显,胶体磷在河口海区的浓度变化趋势及胶体中有机磷和活性磷的比例都与真溶解相接近而与颗粒相差别较大.     

大辽河口营养物基准推导方法

河口富营养化与流域氮、磷营养物的输入直接相关,制定河口营养物基准,可用于控制河口及其近岸海域富营养化,为环境管理的科学决策提供依据。大辽河是渤海最大的入海河流之一,河口污染较为严重;本文采用频数分布法、非参数分析法和实验室模拟压力响应关系法探讨大辽河口及近岸海域营养物基准的推导,最终得到大辽河口总氮(TN)、总磷(TP)及叶绿素a(Chl-a)推荐基准值分别为1.008mg/L,0.067mg/L和1.175mg/m³,以期为大辽河口及其近岸海域富营养化评估和营养物标准制定提供科学依据。     

长江口及其邻近海域2012年3月和7月溶解态铝的分布特征分析

分别于2012年3月和7月对长江口及其邻近海域水体中溶解态铝的分布及其影响因素进行了研究,并在2012年3月至2013年11月期间对长江徐六泾进行了连续观测。结果表明,徐六泾溶解态铝在夏季出现最高值,在冬季呈现最低值,平均值分别为(313±130)nmol/L和(140±43)nmol/L,表现出与径流量相似的季节变化规律。受陆源输入变化的影响,长江口溶解态铝的浓度由近岸向外海逐渐降低,且呈现出明显的季节性差异,即7月明显高于3月。3月表、底层海水中溶解态铝的浓度范围分别为21~129 nmol/L和27~146 nmol/L,平均值分别为(49±21)nmol/L和(59±27)nmol/L;7月表、底层溶解态铝的浓度范围分别为6~332 nmol/L和9~252 nmol/L,平均值分别为(66±69)nmol/L和(83±74)nmol/L。在7月,表、底层溶解态铝呈现显著性差异,底层沉积物的再悬浮可能是造成差异的主要原因。调查结果表明,溶解态铝在长江口呈现出清除型行为,清除主要发生在咸淡水混合初期,初步计算出7月份溶解态铝的清除率约为55%。     

珠江广州河段水环境中多环芳烃的组成及其垂直分布特征

对珠江广州河段白鹅潭水域采集水柱一条,并按 6 层采集水样,根据美国 EPA 标准对多环芳烃进行了定量分析.结果显示,广州河段水环境中多环芳烃和 16 种优控多环芳烃浓度范围分别为 2 602.4 ～ 5 145.2 ng/L和 987.1～ 2 878.5 ng/L;颗粒相和溶解相多环芳烃的含量范围分别为 1 249.3 ～ 3 614.9 ng/L和 919.6 ～ 2 848.8 ng/L.多环芳烃垂向分布特征具有环数越高,其在水柱中下层水体中的含量越高特征,表明水柱可明显分为上层和中下层两层水体,两层水体多环芳烃的组成、污染物的输入方式均有较大的差异,中下层水体高环数的多环芳烃与河口水动力条件密切相关;初步分析表明在涨、落急过程中随流速加大可能引起表层沉积物再悬浮作用造成二次污染.     

胶州湾中汞的含量及其形态的分布规律

1987年5月、9月和1988年1月调查了胶州湾表层海水、浮游植物和表层沉积物中汞含量。溶解无机汞含量的变化范围为0.63—4.4ng/dm~3,溶解总汞含量的变化范围为2.5—40ng/dm~3,浮游植物含量变化范围为1.1—25ng/g(湿重)。测定结果表明,胶州湾中汞含量和分布规律与浮游植物的盛衰和陆地迳流有关。有机汞和COD之间存在着线性关系,溶解无机汞含量随叶绿素a含量增加呈指数下降,表明浮游植物对汞的富集及其在海水中形态的转化起着十分重要的作用。     

海口湾海水重金属的行为特征

本文对海口湾溶解态铜、铅、锌、镉进行了测定.铜的变化范围为:0.47～1.16μg/dm3,平均值为0.78μg/dm3;铅的变化范围为:0.94～2.36μg/dm3,平均值为1.36μg/dm3;锌的变化范围为:1.28～4.83μg/dm3,平均值为3.14μg/dm3;镉的变化范围为:0.005～0.072μg/dm3,平均值为0.030μg/dm3,Cu、Zn的溶解态含量在龙昆路生活污水排污沟口、秀英工业排污沟口及海甸溪口的测站相对较高,Pb、Cd溶解态含量较低,湾内各站平面分布较为均匀.它们的溶解态含量垂直变化趋势为:Cu、Pb、Zn底层大于表层,而Cd表层大于底层.对Cu、Pb、Zn、Cd的颗粒态含量也进行了测定,指出海口湾海水中的颗粒物对重金属的净化起一定作用.对铜的溶解态中的强络合态和不稳态铜也进行了研究,强络合态占总溶解态的比例均在85%以上,对生物起毒性作用有关的不稳态铜含量很低,均小于5nmol/dm3,表明目前海口湾海水中的重金属铜不会对生物生长产生影响.     

夏季辽河口各形态营养盐的河口混合行为

利用2009 年7 月对辽河口水域航次的调查结果, 对该水域营养盐的形态和分布特征进行了探讨,并对其主要控制过程进行了讨论。结果表明： 辽河口水域营养盐的变化范围较大。磷主要以磷酸盐的形式存在, 其余依次是颗粒态磷PP、溶解有机磷DOP, 三者含量相差不大; 氮主要以硝酸盐的形式存在, 其余依次是溶解有机氮DON、颗粒...     

Contribution a l'etude chimique du materiel dissous et particulaire de l'estuaire de la riviere rimouski

Temperature, pH, total alkalinity, dissolved oxygen, silicate, nitrate, phosphate and the Mn, Fe and Al contents of suspended particulate matter (SPM) were measured in the Rimouski River estuary as functions of chlorinity during the period May—September 1980.At any given time, total alkalinity (TA) is conservative within the estuary with respect to chlorinity. However, the total alkalinity (TA) of the freshwater is related to river flow. This is attributed to dilution of the river water with bicarbonate-poor rainwater.Generally, pH follows the same pattern observed for TA in freshwater. Dissolved oxygen is usually more concentrated in freshwater and decreases linearly with increasing chlorinity. Freshwater is always saturated or supersaturated with respect to O₂. Seasonal fluctuations are attributed to temperature variations.There is no evidence for removal of soluble silicate from the freshwater entering the sea. The concentration of silicate in the freshwater is strongly influenced by rainfall. Soil leaching, conditioned by high rainfall increases the concentration of soluble silicate in freshwater. Nitrate behaves similarly whereas phosphate is complicated by the presence of sewage.Analysis of the Mn, Fe and Al contained in the SPM indicates dilution of river-borne particles rich in Mn by others less rich in this element. A decrease in Mn content with increasing chlorinity and SPM concentration as well as increasing concentrations of SPM with increasing chlorinity indicate that the composition is controlled primarily by physical mixing of material from two sources rather than by chemical processes. Within the analytical precision the Fe/Al ratio does not vary with the chlorinity.     

Riverine Composition and Estuarine Geochemistry of Particulate Metals in China—Weathering Features, Anthropogenic Impact and Chemical Fluxes

Suspended sediments from large and middle size Chinese estuaries, including the Yalujiang, Shuangtaizihe, Luanhe, Jiaojiang and Zhujiang, were analysed to understand trace metal transport in the coastal zone. The determinations of 13 major and trace elements plus organic carbon were made of total concentrations and were fully validated by certified reference materials (CRMs). The combination of the data sets with other Chinese estuaries, such as Changjiang and Huanghe, provides an overview of particulate trace metal geochemistry in this region. Trace metal levels in Chinese rivers are relatively low compared with those draining industrialized regions of Europe and North America. In the estuaries, most particulate elements illustrate stable distribution in the mixing zone until a salinity of 30, especially when absolute concentrations are normalized to aluminium, although the total suspended matter (TSM) is quite different in time and space. Using Al as a reference, it was estimated that 25–40% for Cu, and 5–20% for Pb could remain in labile part in the Jiaojiang, Shuangtaizihe and Zhujiang, whereas different features of labile elements were found in the Changjiang and Luanhe. The mean enrichment factor (EF_m) increases with higher sewage to river runoff ratio (S/R) over the drainage basin and EF_m for suspended matter is higher than that for bottom sediments. Finally, inputs of particulate trace metals to the coast are estimated based on the riverine sediment load and chemical compositions.     

中国河口地球化学研究的若干进展

在过去１０年的河口地球化学研究的基础上，总结了中国一些大的河口体系中的化学要素的行为特点。与世界上的大河流相比，中国河流中具有较高的营养元素和较低的痕量元素浓度。流域盆地的风化作用指数由北向南逐渐增加，这与世界上其它地区十分相似。在河口淡－咸水混合过程中，颗粒态的化学要素多呈稳定态分布模式，这与高的泥沙量，较轻的污染程度和水文动力作用相对较弱有关，并县对生态系统有显著的影响。考虑到化学要素在中国河     

The behavior of iron,manganese and silicon in the Peconic River estuary,New York

The behavior of dissolved and particulate iron and manganese and dissolved silicon has been studied as a function of chlorinity in the Peconic River estuary, New York. This study sought to identify important geochemical processes in a relatively pristine estuary facing increasing anthropogenic impact.Dissolved iron behaved in the classical non-conservative manner exhibiting removal of nearly 80% at very low chlorinities, while particulate iron increased by a corresponding amount over the same chlorinity range. Dissolved manganese was enriched by up to 200% over its predicted concentration at low and intermediate chlorinities by desorption from suspended particulates and by a probable benthic flux. Dissolved silicon was enriched by up to 100% at low and intermediate chlorinities also from a probable benthic flux. These fluxes were estimated to be 5 μg cm^?2 day^?1 for dissolved manganese and 70 μg cm^?2 day^?1 for dissolved silicon.The quantity of both particulate iron and manganese increased at high chlorinities due to an influx of suspended inorganic particulates. In the intermediate to high chlorinity region, oxidation of sediment-derived manganese is believed to contribute to the observed increase in particulate manganese.Total iron was essentially conservative throughout most of the estuary, while total manganese was non-conservative presumably due to extensive remobilization of dissolved manganese from the sediments.     

Pattern and annual rates of Scrobicularia plana mercury bioaccumulation in a human induced mercury gradient (Ria de Aveiro, Portugal)

Due to the lack of knowledge regarding annual bioaccumulation rates in estuarine and marine fauna, the main aim of this work was to study the annual mercury bioaccumulation in the well-documented bivalve species Scrobicularia plana along a human induced mercury gradient in the Ria de Aveiro coastal lagoon (Portugal) and in a nearby, non-polluted system (Mondego estuary), parallel to the risks associated with its consumption by humans.Minimum total mercury concentration was as low as 0.019 mg kg⁻¹ (wwt) in 4+ year old organisms in the reference site, where a significant negative correlation (p < 0.05) was found between total mercury concentrations and size, resulting in negative bioaccumulation rates (detoxification). On the other hand, values reached 1.8 mg kg⁻¹ (wwt) in 3+ year old bivalves from the most contaminated area, where a strong positive correlation with size was found (p < 0.01) and annual bioaccumulation rates were as high as 0.25 mg kg⁻¹ yr⁻¹. Annual bioaccumulation rates were highly correlated with suspended particulate matter mercury concentrations. Even though the levels of organic mercury contents increased parallel to the contamination gradient, at each sampling station, no increment was found with age, which corresponded to a decrease in organic mercury percentage with age.In terms of ecological management and public health, the ratio of 0.01 consistently found between Scrobicularia plana annual mercury accumulation rates and SPM mercury levels for most sites may permit to roughly estimate S. plana contamination of commercial sized individuals (>2.5 cm) and, if verified and confirmed in other systems, be used as a simple management tool.     

Dynamics of the turbidity maximum zone in a macrotidal estuary (the Gironde,France): Observations from field and MODIS satellite data

Over a 1-year period, field and satellite measurements of surface water turbidity were combined in order to study the dynamics of the turbidity maximum zone (TM) in a macrotidal estuary (the Gironde, France). Four fixed platforms equipped with turbidity sensors calibrated to give the suspended particulate matter (SPM) concentration provided continuous information in the upper estuary. Full resolution data recorded by the moderate resolution imaging spectroradiometer (MODIS) sensors onboard the Terra and Aqua satellite platforms provided information in the central and lower estuary twice a day (depending on cloud cover). Field data were used to validate a recently developed SPM quantification algorithm applied to the MODIS ‘surface reflectance’ product. The algorithm is based on a relationship between the SPM concentration and a reflectance ratio of MODIS bands 2 (near-infrared) and 1 (red). Based on 62 and 75 match-ups identified in 2005 with MODIS Terra and Aqua data, the relative uncertainty of the algorithm applied to these sensors was found to be 22 and 18%, respectively.Field measurements showed the tidal variations of turbidity in the upper estuary, while monthly-averaged MODIS satellite data complemented by field data allowed observing the monthly movements of the TM in the whole estuary. The trapping of fine sediments occurred in the upper estuary during the period of low river flow. This resulted in the formation of a highly concentrated TM during a 4-month period. With increasing river flow, the TM moved rapidly to the central estuary. A part of the TM detached, moved progressively in the lower estuary and was finally either massively exported to the ocean during peak floods or temporary trapped (settled) on intertidal mudflats. The massive export to the ocean was apparently the result of combined favorable environmental conditions: presence of fluid mud near the mouth, high river flow, high tides and limited wind speeds. The mean SPM concentration within surface waters of the whole estuary showed strong seasonal variations but remained almost unchanged on a 1-year-basis. These observations suggest that the masses of suspended sediments exported toward the ocean and supplied by the rivers were almost equivalent during the year investigated (2005). Results show the usefulness of information extracted from combined field and current ocean color satellite data in order to monitor the transport of suspended particles in coastal and estuarine waters.     

A comparative study of mercury contamination in the Tagus estuary (Portugal) and major French estuaries (Gironde,Loire, Rhône)

Concentrations of mercury were determined for the waters, suspended matter and sediments of the Tagus and of major French estuaries.The Tagus estuary is one of the most contaminated by mercury derived from the outfalls of a chloralkali plant and from other industrial sources. In deposited sediments the median level, 1·0 μg Hg g^?1, is twenty times higher than the natural background and Hg contents depend on the sediment grain-size, age and the distance from waste-outfalls. Suspended matter is more regularly and highly contaminated (median value: 4·5 μg Hg g^?1). In the French estuaries Hg levels in the suspended material decrease with salinity due to dilution and/or remobilization processes. In June 1982, in the Loire estuary, high values of Hg are observed in the middle estuary and attributed to urban and industrial sources.In the Tagus estuary, the general distribution of total dissolved Hg confirms the contamination: it increases seaward from 10 ng 1^?1 in the river to 80 ng 1^?1 in the estuary outlet. The dissolved Hg is almost totally organic in the river, inorganic in the middle estuary due to inorganic Hg effluents and again organic in the lower estuary. This variation is related to the dissolved organic carbon values. The dissolved Hg levels in the Loire Estuary (5–300 ng 1^?1) are much higher than in the Gironde estuary (3–6 ng 1^?1) and of the same order as those observed in the Tagus estuary.     

Suspended particulate matter in the St. Lawrence estuary and Gulf surface layer and development of a remote sensing algorithm

Remote sensing of chlorophyll concentration is potentially affected by the presence of inorganic matter in the water column. Seasonal variability of total suspended particulate matter (SPM) concentration and its partition into organic and inorganic fractions was thus measured in the estuary and Gulf of St. Lawrence during five cruises. These measures were made in the surface layer down to the depth of the 0.1% light level. Results indicate that vertical variability was small for the entire study area. Data analysis lead to the definition of two main regions having different SPM characteristics: 1) the estuary zone characterized by a strong spatial variability, intermediate SPM concentrations and a clear spring phytoplankton bloom that is combined to an increased inorganic matter load; 2) the gulf region characterized by a relatively low SPM concentration and phytoplankton blooms in the spring and fall periods. Combined with in situ measurements of remote sensing reflectances, the database was used to validate existing inorganic matter retrieval algorithms and develop a new one better adapted to the low concentrations encountered in the St. Lawrence estuary and Gulf.     

Distribution and sources of organochlorine pesticides in water and sediments from Daliao River estuary of Liaodong Bay,Bohai Sea (China)

The levels of 19 kinds of organochlorine pesticides (OCPs) in the aqueous phase, suspended particulate matter (SPM), pore water and sediments from Daliao River estuary of Liaodong Bay (Bohai Sea) in northeast China were investigated to evaluate their potential pollution risks. The total OCPs concentrations in the aqueous phase, SPM, pore water and sediments were 3.7–30.1 ng l⁻¹, 4.6–52.6 ng l⁻¹, 157–830 ng l⁻¹ and 2.1–21.3 ng g⁻¹ dry weight, respectively. The concentrations of OCPs, in the Daliao River estuary, are in the mid-range, as compared to those reported in other estuaries worldwide. The distribution of HCHs and DDTs were different indicating different contamination sources. Lindane is the main type of HCH and continuing use in northeast China of ‘pure’ HCH (lindane) rather than technical HCH accounts for the source. The ratios of (DDE + DDD)/DDT in the samples indicate no recent inputs of these chemicals to the estuary.     

Mass balance of lead through a small macrotidal estuary: The Morlaix River estuary (Brittany,France)

Dissolved and particulate lead were measured over an annual cycle (12 surveys between February 1998 and January 1999) in the Morlaix River estuary (Brittany, France). The concentrations were investigated in both the water column and the sediment of the river bottom in relation to hydrological conditions. In the water column, dissolved and particulate lead concentrations ranged from 0.1 to 4.4 nM and from 0.04 to 1.9 μmol g^− 1, respectively. Lead concentrations in surface sediment varied from 0.04 to 0.19 μmol g^− 1 and concentrations in the sediment pore water of the estuary were below the detection limit. Compared with the ranges known for pristine estuaries, concentrations of Pb in the water column of the Morlaix River estuary were found to be much higher. Concentrations of Pb also exceeded the lower range of those known for industrialized estuaries. Extensive agricultural activities in the drainage basin may be responsible for Pb levels above pristine conditions. Furthermore, the sediment appeared not to be contaminated. A mass balance was constructed quantifying all known sources and sinks for the Pb in the estuary. Riverine input accounts for most of the total annual metal flux. Burial in sediments was the major sink within the estuary, which acts as a trap especially for the particulate lead. The mass balance shows that the metal accumulation ranged between 414.6 and 446.0 kg year^− 1.