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1.
The chemical forms and distribution of dissolved arsenic species in the estuary of the River Beaulieu (Hampshire, U.K.) are reported. ‘Inorganic arsenic (V)’ in both the marine and riverine estuary inputs are in true solution, passing through ultrafiltration membranes having a nominal molecular weight cut-off of 500 daltons. Extensive removal of dissolved ‘inorganic arsenic (V)’ is apparent from the distribution of arsenic in the estuary, with laboratory mixing experiments indicating that removal is favoured in the low salinity region. ‘Inorganic arsenic (III)’ and methylated arsenic species account for up to 41% and 70% of the dissolved arsenic, respectively, but are only found during the warmer months when water temperatures exceed ca. 12°C. 相似文献
2.
福建闽南沿海养殖贝类体中砷含量的分布 总被引：9，自引：0，他引：9
通过2003~2004年对福建闽南沿海5种养殖贝类体砷含量的调查监测,对养殖贝类体中砷含量的分布进行了探讨.福建闽南沿海5种养殖贝类体总砷含量为0.65×10-6~4.80×10-6,总平均值为2.09×10-6,其中有机砷和无机砷占总砷含量的百分比分别为61.6%~98.2%和2.3%~38.4%,平均值分别为88.8%和11.2%.在相同养殖区,养殖贝类体总砷平均含量的种间分布差异较小.滩涂养殖底栖贝类体内总砷平均含量总体上高于浅海筏式养殖贝类体的平均含量.福建闽南沿海5种养殖贝类体内总砷含量在泉州湾、湄州湾、东山湾和九龙江口高,在诏安湾和围头湾低,在其余各湾相近.5种养殖贝类体内无机砷的污染指数和总平均值分别为0.05~0.76和0.23,总砷的污染指数和总平均值分别为0.06~0.48和0.21,总体符合国家食品卫生质量标准.养殖贝类体中砷含量与体长之间总体成正相关. 相似文献
3.
Gerhardt F. Riedel James G. Sanders Richard W. Osman 《Estuarine, Coastal and Shelf Science》1987,25(6)
From the distribution of dissolved and solid arsenic species in a contaminated estuarine sediment and measured rates of flux of the various arsenic species we propose an empirical model for the cycling of arsenic between sediments and water column. The chemical form of arsenic in the sediment was largely determined by the redox state of the sediment. Arsenite was the dominant dissolved and solid species in the deeper reduced sediment, and arsenate was dominant in the oxidized surface layer. Arsenite in the interstitial water diffused toward the surface layer, where it was mostly oxidized to arsenate prior to leaving the sediments. Some arsenate adsorbed to the surface sediments and produced a surface layer enriched in arsenic. Small concentrations of methyl and dimethyl arsenic were produced in the sediments, and these also diffused into the overlying water.Nereis succinea, a burrowing polychaete, affected distribution and flux of arsenic from the sediments by its production of irrigated burrows. These burrows increased both the effective surface area of the sediment and the diffusion of arsenic by a factor of five. When the relative effects of the activities of Nereis succinea and physical resuspension are compared, results indicate that although physical resuspension can produce large pulses of materials from contaminated sediments, continuous biological activity is likely to be more important in the mobilization of contaminants from sediments in many estuarine environments. 相似文献
4.
With the rising cost of oil the electric power generating companies are turning to coal as a fuel source. Large amounts of fly ash are produced as a by product of coal combustion. This fly ash must then be disposed of, with the oceans being considered an alternative to land fill disposal. This research investigated the sorptive behavior of the surface-associated arsenic and utilized the results to project arsenic's impact on the water column during the ocean disposal of fly ash.Several acid digests were investigated to determine an effective method of arsenic recovery from fly ash. Of these, the HCl digest was the most effective technique, yielding 100% arsenic recoveries from fly-ash particles. The arsenic content of the fly ashes studied varied from 69 ± 11 μg g−1 to 323 ± 24 μg g−1, reflecting differences in the arsenic content of the source coal. In both seawater and freshwater there is an increase in arsenic desorption with increasing pH. The greatest release of arsenic occurred at pH 12 with generally over 80% of the surface arsenic released.Fly ash in contact with seawater and freshwater can exhibit either acidic or alkaline tendencies depending upon the soluble elemental composition on the surface of the flyash particle. The acidic ashes were shown to leach a greater percentage of arsenic (16.9%) than the more alkaline ashes (8.2%). During these leaching studies in seawater, arsenic was found to leach in both the pentavalent and trivalent oxidation state. The pentavalent state was predominant, comprising 77% of the arsenic initially desorbed.The dissolution in seawater of arsenic was utilized to assess the possible impact of the ocean disposal of fly ash. Based upon these data it appears that the natural levels of arsenic in the water column would not be significantly increased. Further research is needed on the fate of fly-ash particles in marine sediments. 相似文献
5.
James T. Byrd 《Marine Chemistry》1988,25(4)
Arsenic concentrations vary with season on the continental shelf of the South Atlantic Bight. During periods of high winds in the winter and early spring, inorganic arsenic concentrations are reduced to as little as 20% of typical open ocean concentrations by sorption onto resuspended sediments or incorporation into phytoplankton. In the early fall, arsenic sequestered in sediments in the spring is regenerated and returned to the water column, creating elevated arsenic concentrations in the nearshore zone that are up to 50% greater than open ocean concentrations. Arsenic in the adjacent estuaries is nearly conservative over the seasonal cycle, although its distribution in the estuaries is greatly affected by the seasonal changes in arsenic concentrations in the nearshore waters. 相似文献
6.
Dennis G. Waslenchuk 《Marine Chemistry》1978,7(1):39-52
The concentrations of arsenic species in continental-shelf waters of the southeastern U.S. are controlled mainly by simple physical mixing of shelf waters and Gulf Stream intrusions. The biota mediate redox reactions which result in a disequilibrium of arsenic species; up to 20% of the total arsenic (averaging 1.1 μg/l) occurs as unstable arsenite [As (III)] and dimethylarsenic, the remainder consists of thermodynamically favored arsenate [As (V)]. Uptake of arsenic by the biota has a minor effect on arsenic distribution in offshore waters, producing a deep-water arsenate maximum, and minima for arsenite and dimethylarsenic. Riverine and atmospheric arsenic inputs to the shelf waters are relatively insignificant. Southeastern rivers contain only about 0.3 μg/l dissolved arsenic, and the atmosphere adjacent to continental shelf waters contains about 1.7 ng/m3 of As (V), exclusively associated with the particulate fraction. 相似文献
7.
Markus Stoeppler Mechthild Burow Friedrich Backhaus Winfried Schramm Hans Wolfgang Nürnberg 《Marine Chemistry》1986,18(2-4)
A long-term study within the pilot environmental specimen bank programme of the Federal Republic of Germany on arsenic levels in coastal and open seawater and their reflection in the brown seaweed (Fucus vesiculosus) has been performed. Dissolved arsenic was on average 0.76 (range 0.45–1.11) μgl−1 for 17 sampling stations in the Baltic Sea, whereas contents of dissolved arsenic are somewhat higher in shallow waters of the coastal zone of the North Sea. Total arsenic levels in algae ranged up to 40 mg kg−1 (dry weight) and showed for the four locations studied obvious seasonal variations for comparatively nonpolluted or nondisturbed locations only. However, probably due to biological influences, the results obtained so far indicate that composite samples integrating a one year period are supposed to be the best strategy for future environmental specimen banking. Using a new efficient speciation technique the percentage of chemically stable organoarsenic compounds in the investigated algae has been found to be 95% of the total arsenic content and thus somewhat lower than in teleost fish. For comparison, typical data for a few other algae species from the Baltic and the Mediterranean Sea are also shown. 相似文献
8.
The conservative potential of arsenic in the relatively pristine waters of Galway Bay, an estuarine system in the west of Ireland, is examined through the inter-seasonal variations in the distribution of its total, hydride and non-hydride fractions. The arsenic concentrations in Galway Bay and local fresh water sources at all seasons were lower than what is considered the natural seawater concentration of 2 μg L−1 (27 nM). The effects of physical mixing, biological uptake and regeneration of arsenic on its distribution are considered. The degree of biological uptake and regeneration of the element are determined by a first order speciation between total arsenic (a small part of which should be of organic origin) and hydride arsenic (mostly of inorganic origin). The structural similarity of arsenic species to phosphate in seawater causes arsenic to be taken up by biota, which then have to detoxify it, so results are presented against phosphate to determine the degree of biological transformation of arsenic at different seasons. An in-house, batch type system of hydride generation coupled to electro-thermal atomic absorption spectrometry is used for the analysis of arsenic; this is preceded by UV-digestion prior to the measurement of total arsenic. Results show only a small association of arsenic with phosphate but a near linear, positive distribution pattern between arsenic and salinity in Galway Bay (R2 ∼ 0.6), which is reproducible among seasons, indicating that in this environment the biological uptake of arsenic is likely to be a much slower process than the physical mixing of the water masses. 相似文献
9.
An automatic flow analysis system with on-line liquid nitrogen trap, hydride generation and flame-less atomic absorption spectrophotometry was presented for the determination of inorganic arsenic and antimony in seawater. The experimental conditions such as acidity of reduction reaction, the amount of sodium borohydride , the flow rate of carry gas (high purity of nitrogen) were tested and selected optimally. The limit detection of the method presented was 0. 15 ug/L for arsenic and 0. 24 μ/L for antimony . During the determination of seawater samples with levels microgram arsenic and antimony pa litre th?variation coefficient would be ±4% for arsenic and ±10% for antimony. The volume needed for one measurement was 9 mL for arsenic and 12 mL for antimony. The frequency of sample determination reached 20 times per hour for arsenic and 15 times per hour for antimony. 相似文献
10.
采集九龙江河口表层和柱状沉积物样品,对表层沉积物中总砷、不同形态砷和其他重金属元素、有机质含量以及粒径等参数进行测定.分析了柱状沉积物中总砷和各形态砷的含量,结合沉积速率和响应因子,探讨总砷的污染累计特征.结果表明：（1）沉积物中检出的形态砷是As3＋和As5＋,未检出有机砷.（2）表层沉积物中总砷含量范围为10.03～11.29μg/g,河端总砷含量为11.28μg/g,高于海端总砷含量10.42μg/g.As3＋的含量范围为0.84～1.08μg/g,As5＋的含量范围为6.87～8.99μg/g;As5＋含量表现为河端（8.63μg/g）高于海端（7.31μg/g）,As3＋则不明显.（3）有机质含量是影响本区域表层沉积物中砷及其他重金属含量分布的重要因素,粒径与砷及其他重金属显著相关性不强,影响较小.（4）柱状沉积物中总砷含量范围为9.15～13.61μg/g,随深度的变化不明显,人为污染程度较轻.（5）柱状沉积物中As3＋含量介于2.45～5.35μg/g之间,As5＋含量范围为5.58～11.77μg/g,二者含量随深度的增加而降低. 相似文献
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12.
James G. Sanders 《Marine environmental research》1980,3(4):257-266
The arsenic cycle in productive, near-shore marine systems is complex, involving both geochemical inputs and outflows and biological mediation. The major input to the Georgia Bight is intrusion of subsurface Gulf Stream water; in other marine systems, river run-off and atmospheric deposition may provide a large percentage of the arsenic input. Indiscriminate biological uptake is responsible for changes in arsenic speciation, involving approximately 20% of the dissolved arsenate pool and resulting in measurable concentrations of reduced and methylated arsenic species. The overall cycle is similar to the phosphate cycle; however, regeneration time for arsenic is much slower. 相似文献
13.
Replicate portions of a Delaware salt marsh were enclosed in cylindrical microcosms and exposed to elevated levels of inorganic arsenic (arsenate). All biotic and abiotic components in dosed cylinders rapidly incorporated arsenic. Spartina blades showed the greatest arsenic enrichment, with dosed plants incorporating arsenic concentrations an order of magnitude higher than controls. Spartina detritus and sediments also exhibited greatly elevated arsenic concentrations. Virtually all of the arsenic was incorporated into plant tissue or strongly sorbed to cell surfaces. Thus, elevated arsenic concentrations in estuarine waters will be reflected in living and non-living components of a salt marsh ecosystem, implying that increased arsenic will be available to organisms within the marsh ecosystem. 相似文献
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16.
Axenic cultures of the microalgae species, Dunaliella tertiolecta and Phaeodactylum tricornutum were grown at arsenic (As) concentrations typically found in uncontaminated marine environments ( 2 µg L− 1) under different phosphorus concentrations. D. tertiolecta accumulated higher arsenic concentrations (mean: 13.7 ± 0.7 µg g− 1 dry mass) than P. tricornutum (mean: 1.9 ± 0.2 µg g−1 dry mass). Media phosphorus concentrations (0.6–3 mg/L) had little influence on microalgae growth rates or arsenic accumulation. Arsenic was present as lipid bound (29–38%; 4.2–9.5%), water-soluble (20–29%; 26–34%) and residue bound (41–45%; 57–69%) arsenic species in D. tertiolecta and P. tricornutum respectively. Hydrolysed lipids contained mostly glycerol arsenoribose (OH- ribose), dimethylarsinate (DMA) and inorganic arsenic (As(V)) moieties. Water-soluble species of microalgae were very different. D. tertiolecta contained inorganic arsenic (54–86%) with variable amounts of DMA (7.4–20%), arsenoriboses (5–25%) and traces of methylarsonate (MA) ( 1%). P. tricornutum contained mostly DMA (32–56%) and phosphate arsenoribose (PO4-ribose, 23–49%) and small amounts of OH-ribose (3.8–6.5%) and As(V) (9–16%). Both microalgae contained an unknown cationic arsenic species. The residue fractions of both microalgae contained predominately inorganic arsenic (99–100%). These results show that at natural seawater arsenic concentrations, both algae take up substantial amounts of inorganic arsenic that is complexed with structural elements or sequestered in vacuoles as stable complexes. A significant portion is also incorporated into lipids. Arsenic is metabolised to simple methylated species and arsenoriboses. 相似文献
17.
渤海莱州湾表层沉积物中金属元素分布及环境质量 总被引：3，自引：1，他引：2
利用X-射线荧光光谱仪、等离子质谱仪或原子荧光光度计测定了莱州湾表层沉积物中金属元素的含量,探讨了它们的分布特征、来源及污染程度,结果表明,沉积物中铜、锌、铅、镉、砷、镍、铬、钴、钒、钪、铁、锰的含量由近岸向湾内递减,莱州湾北部海域的含量大于南部的。银含量高的沉积物主要分布在莱州湾中部偏西南的环流中心区。沉积物中砷和镍含量超过ERL值,潜在生态风险较高。富集系数和主成分分析显示,沉积物中铁、铜、锌、镉、砷、铬、镍、钴、锰、钒和钪为无富集,砷为轻度富集,铅和银为中度富集。铁、铜、锌、镉、铬、镍、钴、锰、钒、砷和钪主要来源于自然源,铅既有岩石和土壤风化产物硅酸盐矿物等自然源的贡献,又受到了人为活动的影响,银主要受人为活动的影响。聚类分析表明,可把莱州湾沉积物分为4类,其中黄河口西北缘沉积物中砷和镍污染生态风险最高,其次是莱州湾中部和北部。 相似文献
18.
Chemical extraction techniques show that the majority of the arsenic in North Atlantic deep-sea sediments is associated with an iron phase compositionally similar to that found in deep-sea ferromanganese nodules (As/Fe ～ 11 · 10?4) and is probably of seawater origin. Some sediments also contain As associated with Fe oxides produced by continental weathering. A minority (～8%) of the arsenic is of detrital origin but is not associated with Fe or Mn oxides; it has a content (1.7 ppm) similar to the average crustal abundance. In the Eastern Mediterranean Sea, near-shore sediments contain As associated with land-derived Fe oxides (As/Fe ～ 2 · 10?4), but As/Fe ratios increase to ～ 13 · 10?4 in deep-sea sediments as the contribution of seawater derived arsenic becomes dominant. Arsenic is enriched in metalliferous sediments (As/Fe ～ 20?50 · 10?4) but As/P ratios of metalliferous sediments, deep-sea ferromanganese nodules and deep-ocean water are all similar. Although a hydrothermal contribution cannot be discounted, it is likely that the arsenic is also of seawater origin, suggesting that hydrothermal iron oxyhydroxides remove As more efficiently from seawater than do iron phases (goethite) in deep-sea sediments and nodules. Arsenic accumulates in deep-sea sediments (～ 6 μg cm?2 10?3 yr?1) at sediments (～ 120 μg cm?2 10?3 yr?1) at rate sufficient to balance river input input (～3 · 1010 g yr?1). These estimates give an oceanic residence time for arsenic of 1–2 · 105 yr. 相似文献
19.
胶州湾东部水体、浮游植物和沉积物中的砷 总被引：2，自引：1，他引：2
根据胶州湾四个航次中水体的溶解态总砷c（AS）、溶解态三价砷c（AS（Ⅲ））、悬浮物总砷（Asp）、浮游植物总砷（Asph）、沉积物酸萃取态砷（SAsH）的调查数据，指出c（As）含量未超过国家一类海水水质标准，其高值区位于四方近岸，并由近岸向远岸浓度逐渐降低。由悬浮颗粒物、浮游植物和沉积物对水体中砷的富集因子，指出三者在砷的循环和迁移中起主导作用。 相似文献
20.
Arsenic geochemistry in Chesapeake Bay: Dependence upon anthropogenic inputs and phytoplankton species composition 总被引：1，自引：0，他引：1
James G. Sanders 《Marine Chemistry》1985,17(4):329-340
Arsenic is not conservative in Chesapeake Bay. Inputs of man-derived arsenic, of the order of 100 kg d−1, cause substantial positive deviation from theoretical dilution. The chemical form of the arsenic varies both seasonally and along the axis of the bay. During winter, arsenic is present only as arsenate. During summer, substantial quantities of reduced and methylated forms are present in different areas, indicative of separate formation processes. Arsenite, present in low-salinity regions, may have been formed by chemical reduction in anoxic, subsurface waters and then mixed into the surface layer. Methylated arsenicals correlate highly with algal standing stocks. One particular form, methylarsonate, is highly correlated with the dominant algal genus, Chroomonas. As both arsenic reactivity and toxicity are altered by transformation of chemical form, the observed variations in arsenic speciation have considerable geochemical and ecological significance. 相似文献