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1.
In this study, 36 fish species were collected from three coastal cities in Korea to investigate levels and patterns of six arsenicals (arsenite: As (III), arsenate: As (V), arsenocholine: AsC, arsenobetaine: AsB, monomethylarsonic acid: MMA, and dimethylarsinic acid: DMA). The levels of ∑6 As in the different fish species varied substantially, ranging from 0.02 μg As/g ww (Islaeli carp) to 9.65 μg As/g ww (Skate ray) with a median of 0.40 μg As/g ww. All the arsenicals in marine fishes showed higher levels than those in freshwater fishes due to fish feed living in saline water. Overall, marine carnivorous fishes seem to be more contaminated with arsenic. For all the fish samples, AsB (mean fraction: 90.6%) was dominant among the six arsenicals, indicating biomethylation of inorganic arsenic and accumulation of AsB. Fish species with high water contents showed elevated levels of As (III), but there was no further significant correlations between arsenicals and water/lipid contents. Concentrations of As (V) were significantly lower than those of As (III), which implies that As (V) is reduced during biomethylation of inorganic arsenic. Consequently, we hypothesize that the toxicity of arsenic (mainly derived from As (III)) can be increased by the reduction of As (V), especially for the fish species with higher water contents.  相似文献   

2.
《Oceanologica Acta》1998,21(2):325-333
The arsenic (As) cycle in the marine environment is known to be sensitive to biological activity. Within the scope of the National Coastal Oceanography Program, we undertook a specific study of the behaviour of this element in a water column on the continental shelf of the Bay of Biscay off the Gironde estuary during two oceanographic cruises conducted in May 1994 and May 1995. Various chemical forms were measured: arsenate (As3), arsenate (As5), monomethylarsenic (MMA), dimethylarsenic (DMA) and dissolved total As after ultraviolet mineralization. The net flux of total As from the Gironde estuary was evaluated as well as its effect on the concentration in surface marine waters. The vertical profiles in the coastal zone during a period of active primary production confirmed a certain analogy between arsenates and phosphates as well as the formation of As3 and DMA. The importance of organoarsenic species not directly accessible to the formation of volatile hydrides is demonstrated. Their presence modifies assessments, reducing the deficit of dissolved total As in the euphotic layer to just 5%. For particles, the As content in phytoplankton was estimated at 6 μg·g−1 compared to 20 to 30 μg·g−1 in iron- and aluminium-rich terrigenous particles. These results do not invalidate the role of phytoplankton in the speciation of dissolved As but indicate that their involvement in vertical transfers was apparently not predominant in the zone under study.  相似文献   

3.
本文综合2000～2003年期间9个航次的研究结果，讨论了总溶解态无机砷（TDIAs，[TDIAs]=[As^5＋]＋[As^3＋]）和亚砷酸盐（As^3＋）在黄、东海的分布和季节性变化。调查海区覆盖了黄、东海不同水文和化学性质的区域，研究重点放在自长江口向东南琉球群岛沿伸的PN断面以讨论陆源输送的物质对中国陆架边缘海的影响。利用氢化物发生原子荧光光谱法（HG-AFS）分析砷的不同形态（TDIAs，As^3＋）。TDIAs受河流陆源输送的影响在近岸区域含量较高，并随着离岸距离的增加含量逐步下降。在东海陆架坡折带的近底层水中也存在TDIAs的高值中心，此区域具有低温、高盐、低悬浮颗粒物含量的特征，显示出入侵陆架的黑潮水是陆架区TDIAs另一个主要的源。TDIAs的季节性变化趋势受到长江冲淡水水量及黑潮入侵陆架强度的季节及年际变化共同影响。研究区域中As^3＋的分布特征与TDIAs相反，其含量、分布及季节性变化受到浮游植物活动的影响，表现出与叶绿索含量存在正相关关系。夏季东海陆架PN断面中As／P的化学计量比值约为2×10^3。黄、东海溶解态砷的含量与世界其它海区相近，表明其未受到明显人为活动的影响。  相似文献   

4.
Total arsenic, arsenate and arsenite concentration profiles for the water column of Saanich Inlet, an intermittently anoxic fjord located on Vancouver Island, B.C., Canada, were measured using independent analytical techniques for total arsenic and arsenic speciation to evaluate the accuracy of the speciation technique in both oxic and anoxic marine environments. Total arsenic profiles indicate a mid-depth minimum of about 1.0 ppb above the oxic—anoxic interface and an enrichment in the anoxic zone to about 2.0 ppb. This minimum may be due to either advection of arsenic-poor water into Saanich Inlet at mid-depth or arsenic incorporation onto solid phases within a bacteria- and manganese-rich particulate layer located immediately above the oxic—anoxic interface and subsequent removal via sinking particulate material. Ratios of total arsenic to phosphorus in the deep, anoxic waters of the basin are similar to those reported for marine algae, suggesting that the enrichment of total arsenic within the anoxic bottom layer may be due to its release upon organic matter decomposition.Arsenate and arsenite concentration versus depth profiles indicate a rapid (but incomplete in a thermodynamic sense) response to the oxic—anoxic interface. The arsenate/ arsenite concentration ratio is 15/1 in the oxic region of the water column and 1/12 in the anoxic zone. Arsenate—arsenite interconversion occurs at a depth shallower than ferric-ferrous but deeper than MnO2 —Mn2+ interconversions.Measurements of arsenite oxidation rates at near-ambient arsenite concentrations and temperatures using an 74As3+ radioactive tracer technique indicate that arsenite oxidation is initially ten times faster in seawater taken from the manganese-rich particulate layer at 165 m depth than in seawater collected near the surface at 50 m depth. Addition of antibiotics to seawater from 165 m depth initially suppressed the rate of arsenite oxidation, indicating that it may be partially microbially mediated.  相似文献   

5.
The content and the oxidation state of arsenic and antimony in coastal seawater were determined coupled with chemical separation and neutron activation method. The contents of arsenic and antimony in coastal seawater were estimated to be 1.56–2.73g As/l, 0.25–0.57g Sb/l. Most parts of these elements exist as soluble ionic species, passing through 0.45 pore-size membrane filter, and at surface, 80–97% of arsenic occurs as arsenate and 70–94 % of antimony may occurs as antimonate. The vertical distribution of arsenite and arsenate is almost constant from the surface to 1,200 m depth. However the distribution of Sb(III) and Sb(V) is much more complicated with depth.  相似文献   

6.
Arsenic compounds in the marine polychaete Arenicola marina collected from Odense Fjord, Denmark were determined by HPLC-ICPMS. In contrast to most other marine animals, A. marina contained most of its water soluble arsenic as inorganic forms, arsenite (58%) and arsenate (16%), and arsenobetaine was present as a minor constituent (6%) only. Other arsenic compounds detected in A. marina were dimethylarsinate (4%), two arsenosugars (1 and 3%), tetramethylarsonium ion (1.5%), and arsenocholine (<1%). A new arsenobetaine -trimethylarsoniopropionate-previously only reported in fish, was also present at trace levels (<1%), and an unknown anionic arsenical (approximately 10%) remains unidentified. When A. marina was exposed in laboratory experiments to different concentrations of arsenate in seawater (10, 50. 100, 500 and 1000 microg As 1(-1)) the polychaetes accumulated arsenic in a dose dependent. non-linear manner. Most of the accumulated arsenic was biotransformed to arsenite and dimethylarsinate. with the remainder being accumulated as unchanged arsenate. None of the other arsenic compounds naturally present in A. marina increased in concentration following arsenate exposure.  相似文献   

7.
Measurements of total dissolved arsenic (As(III+V)) and antimony (Sb(III+V) and their simple methylated species are presented for samples collected from three vertical profiles and along three surface transects in the Chatham Rise region, east of New Zealand. As(III+V) concentrations showed a slight increase with depth (16–17 nM at 25 m to 20 nM at 100 m) whereas Sb(III+V) concentrations were conservative with depth (1.02–1.12 nM). Along the three surface water transects, As(III+V) and Sb(III+V) concentrations showed little variation, with average concentrations of 18±2 and 0.99±0.05 nM, respectively. Inorganic arsenic was not correlated with orthophosphate (r2=0.01). Monomethyl- and dimethyl-arsenic (MMAs, DMAs) concentrations (0.04–0.01 and 0.65–0.07 nM, respectively) decreased with depth, suggesting surface water production by biota and degradation at depth. Along the Chatham Rise transect, DMAs concentrations increased on the Rise (0.65 nM maximum) compared to waters north and south of the Rise (∼0.22 nM). Fluctuation in MMAs concentrations were also seen for water samples collected on the Chatham Rise. Monomethyl-, dimethyl- and trimethyl-antimony (MMSb, DMSb, TMSb) species were detected in water samples collected along all the three surface water transects suggesting surface water production by biota. Concentrations of MMSb, DMSb and TMSb in water samples were fairly constant along all the three surface transects (0.06–0.07, 0.015–0.025 and 0.005–0.015 nM, respectively), showing no significant enrichment on the Chatham Rise. These arsenic and antimony results support the current global view that inorganic As and Sb are conservative and the methyl species are of biological origin.  相似文献   

8.
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   

9.
The distribution of dissolved and participate concentrations of As, Cr and V was investigated in the mixing area of the Po river in five surveys over the period March 1992-March 1995. The data obtained indicate noticeable contamination of coastal waters of the northern Adriatic with Cr but not As or V. Total dissolved concentrations for As and V were comparable with oceanic levels but were higher by a factor of 4 for Cr. These results suggest either low anthropogenic inputs of As and V, from terrigenous and atmospheric sources, or efficient removal mechanisms. The investigated metals had low reactivity during freshwater-seawater mixing and the distribution of concentrations in the dissolved and solid phases suggests that the dilution process is the main factor controlling the transport of these metals to the sea in low-to-medium solid transport conditions. Further investigations are required to elucidate the behavior of these metals during high solid transport conditions. Significant changes in the speciation of As occurred during the transition between the two end-member matrices. In the coastal waters of the northern Adriatic, the arsenite fraction in winter, and the arsenite and dimethylarsinate fractions in summer increased with respect to riverine waters. Changes in the speciation of chromium were minor, but also showed a small increase in reduced species in marine waters.  相似文献   

10.
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   

11.
Continuous CTD data from a series of recent cruises show that the distribution of the water mass characteristics in the central Benguela region from the Orange River mouth (28°38'S) to alvis Bay (22°57'S) is discontinuous in the central and intermediate waters at about the latitude of Lüderitz (26°40'S), Namibia. The central and intermediate water masses at the shelf edge and shelf break north of the Lüderitz upwelling cell have a high salinity relative to the potential temperature compared to similar waters south of the upwelling cell. It is shown that the feed waters for the wind-induced upwelling on the shelf to the north and south of the Lüderitz discontinuity are different in character and source. The distribution of the water masses shows that the shelf-edge poleward undercurrent provides low-oxygen water from different regions in the Atlantic Ocean to be upwelled onto the shelf. North of th Lüderitz upwelling cell, the central and intermediate waters come from the oxygen-depleted Angola Basin, whereas south of the discontinuity those waters are from the interior of the adjacent Cape Basin, which is less oxygen-deficient. This has implications for the dispersion of low-oxygen water and the triggering of anoxic events, and consequences for the biota on the shelf, including commercially important fish species.  相似文献   

12.
《Marine Chemistry》2005,93(2-4):81-103
Surface water transects and vertical profiles for dissolved iron, macronutrients, chlorophyll a (Chl a), and hydrographic data were obtained in the Peru upwelling regime during August and September 2000. The supply of the micronutrient iron, relative to that of the macronutrients nitrate, phosphate and silicic acid, is shown to play a critical role in allowing extensive diatom blooms to develop in the Peru upwelling system. The extremely high-chlorophyll “brown waters of Peru” (with Chl a concentrations between 20 and 45 μg/l) result from massive diatom blooms with maximal photochemical efficiencies (Fv/Fm >0.6) occurring in the iron-rich upwelling region observed over the broad continental shelf off northern and central Peru. The source of the upwelled water in this region is the nutrient-rich subsurface countercurrent in contact with the organic-rich shelf sediments. This subsurface shelf water is suboxic and has extremely high concentrations of dissolved Fe (>50 nM) in the near-bottom waters. In marked contrast, relatively low-chlorophyll “blue waters” (Chl a <2 μg/l) with low concentrations of dissolved Fe (<0.1 nM) and high unutilized macronutrient concentrations are observed in the coastal upwelled waters along the southern coast of Peru and in the offshore regions of the Peru Current. Southern Peru is a region without a wide shelf to serve as a source of iron and, as a result, dissolved Fe concentrations in the near-bottom suboxic waters of this region are an order-of-magnitude lower than observed off northern and central Peru. In addition, the offshore Peru Current is a broad, Fe-limited, high-nitrate, lower than expected chlorophyll region extending hundreds of kilometers offshore into the northeast region of the South Pacific subtropical gyre and northwestward into the South Equatorial Pacific.  相似文献   

13.
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   

14.
利用氢化物发生-原子荧光光谱法(HG-AFS)对2007年3月30日至4月23日南黄海海域总溶解态无机砷(TDIAs,[TDIAs]=[As5+]+[As3+])的含量进行了测定,其中针对水华中心区域(BM1站)进行了25h的连续观测,以探讨春季水华对有毒类金属元素砷的生物地球化学行为的影响。结果表明,TDIAs的浓度范围为7.9~22.3nmol/L,平均值为(17.8±1.9)nmol/L。TDIAs在南黄海的分布主要表现为由近岸向外海逐渐升高的趋势,最大值出现在南部海域底层海水中。近岸海域表、底层TDIAs的含量相当,而中、南部海域由于存在明显的密度跃层,表、底层TDIAs的浓度具有显著性差异。2007年3月31日至4月1日研究区域西南部受到沙尘天气和降雨的影响,表层海水中TDIAs的含量显著升高。研究区域中、南部海域在观测期间暴发了典型的黄海春季水华,通过大面观测和对重点区域的连续观测可以发现,水华期间TDIAs的分布和磷酸盐类似,与Chl a呈现出较好的负相关关系(r=0.51,P0.05,n=39)。经初步计算,浮游植物水华对10m以上表层水体中TDIAs的清除量约为2.4nmol/L,占表层保有量的15%左右。通过箱式模型计算得出黄海TDIAs的停留时间约为(18.2±8.5)a,远远低于大洋。通过对该海域砷、磷摩尔比值的计算可以发现,南黄海砷、磷摩尔比值约为大洋中的20倍左右,这可能会引起浮游生物对砷酸盐的大量吸收和转化,从而带来潜在的生态危机,需要引起足够的重视。  相似文献   

15.
本文研究了0010号台风“碧利斯”影响期间及其随后的恢复期中,厦门港湾中九龙江口和西港海域站表层海水总溶解砷（TDIAs)、As^3 含量和As^3 /As^5 值的变化特征。结果表明,观测期间两站TDIAs和As^5 含量均比非台风时期呈数倍增加,经10d后仍未恢复到非台风时的水平。As^3 含量也有较大幅度的增加,但波动较大。文中还对观测期间影响溶解无机砷含量的因素进行了初步的探讨。  相似文献   

16.
By combining field observations with a statistical approach and a simple but effective estuarine analogue, the main features of the cycling of arsenic in the Tamar estuary have been elucidated. As(III) and As(V) enrichment in the water column is due to a combination of localized inputs and effective recycling of sediment interstitial waters. The profiles of As(V) are similar to those of NH4+ and are dominated by an estuarine maximum resulting from an input from the sediments. As(III) profiles are correlated with those of dissolved manganese and exhibit both fresh water and estuarine maxima. As(III) appears to be effectively removed at the freshwater/brackish water interface by a combination of heterogenous oxidation, catalysed by hydrous manganese dioxide, and adsorption on to iron oxyhydroxide. The estuarine distribution of As(III) within the water column is consistent with the published rates of oxidation of As(III) to As(V) by both inorganic and microbiological processes. The reduction of As(V) to As(III) in the sediments is incomplete. On the basis of our observations a tentative estuarine arsenic cycle is presented.  相似文献   

17.
我国近海镉的水质基准及生态风险研究   总被引：3，自引：1，他引：2  
以镉为研究对象,在分析我国海水水生生物区系特征的基础上,筛选了栖息我国境内的海水水生生物物种的毒性数据,采用基于物种敏感度分布(SSD)模型不同拟合曲线(log-logistic、log-normal、 Gumbel、Weibull和Burr Ⅲ)的方法分别推导了保护水生生物的海水水质急性基准值和慢性基准值,并分析了引入淡水数据推导海水水质基准的可行性;同时,结合我国海水中镉的分布特征,对海水中镉的生态风险了初步评价。结果表明:Burr Ⅲ对各组数据拟合的效果最佳;引入淡水数据可能会对海水生物造成"过保护"风险;基于Burr Ⅲ对海水数据所推导的急性和慢性基准推荐值分别为63.0 μg/L和8.0 μg/L;将我国近岸水体中镉的浓度与基准值比较显示,我国近岸水体中镉对水生生物的潜在风险较低。研究结果有望为我国水质基准研究及标准制定提供参考。  相似文献   

18.
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   

19.
Soluble uranium concentrations in the Ogeechee and Savannah Rivers are 0.046 ± 0.005 and 0.026 ± 0.01 μg/l, respectively. Particulate concentrations are approximately similar in the Ogeechee River but are about four times the soluble concentration in the Savannah River. River end-member 234U/238U ratios range from 1.04 ± 0.04 to 1.08 ± 0.12. Observations suggest that uranium is removed from estuarine waters at low salinities during low discharge.  相似文献   

20.
三价砷和五价砷对鱼类乙酰胆碱脂酶的体外抑制比较   总被引：1，自引：0，他引：1  
为开展水产品中三价砷的酶法快速检测工作,文中研究了三价砷(As3 + )、五价砷(As5+ )对8种鱼脑中乙酰胆碱酯酶(AChE)的抑制率。结果发现,在10 -7～10 -4mol/L范围内,草鱼和鲫鱼脑中AChE的抑制率与三价砷的浓度负对数值有较好的线性关系,相关系数都在0 .97以上;在10 -6～10 -4mol/L范围内,黑、马鲛、鲈鱼脑中AChE的抑制率与三价砷的浓度负对数值的线性相关系数大于0 .99。对于三价砷,由IC50 得到AChE的敏感性为:美国红鱼>草鱼,鲫,鲈鱼>黑,马鲛>鲤,白鲢。鱼种不同,AChE受到的三价砷、五价砷的抑制作用也不同。在浓度为10 -6～10 -4mol/L范围内,三价砷、五价砷对8种鱼脑中AChE的抑制作用存在极显著差异(p <0 .0 1) ,三价砷对AChE的抑制作用远大于五价砷的抑制作用。  相似文献   

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