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Assessment of Water Quality in Estuarine and Coastal Waters of England and Wales Using a Contaminant Concentration Technique

机译:利用污染物浓缩技术评估英格兰和威尔士河口和沿海水域的水质

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Water samples were taken from over 40 estuarine, nearshore and offshore sites in the U.K. during two CEFAS research cruises in 1993. The samples were processed using a bulk hexane extraction and concentration procedure and bioassayed using the marine harpacticoid copepod Tisbe battagliai. This process allowed the toxic effects of non-polar organic contaminants to be measured at all sites, expressed as the concentration factor required to elicit a 48 h median lethal response. Total hydrocarbons (THC) and polycyclic aromatic hydrocarbons (PAH) were also quantified to estimate their contribution to sample toxicity. Extracted contaminants were concentrated < 10-300-fold for estuarine sites, 100-600-fold for nearshore sites and 350- > 1000-fold for offshore sites before toxicity was observed. A tentative water contamination ranking of the studied estuaries was established as Tees > Wear > Mersey > Tyne > Blyth, Poole Harbour, Southampton Water > Ribble, Dee, Lune. Chemical analysis revealed a weak but statistically significant correlation (—0.36 to —0.43) between total hydrocarbon concentrations in water and the concentration factor required to elicit a median lethal response. There was no correlation between a control determinand, algal fluorescence and toxicity. The results indicate that hydrocarbons may make a significant potential contribution to the toxicity of estuarine and coastal waters with a selected 10 PAH compounds estimated to be responsible for up to 18% of the total toxicity at one specific site. However, the cause of the majority of the toxic response remains unidentified. Although the technique is based on an acute endpoint, the high concentration factors required at near and offshore sites suggest that hexane extractable contaminants were not present at chronically toxic concentrations in the untreated seawater. However, at some estuarine sites, low concentration factors ( < 200-fold) suggested that these waters may be exhibiting chronic biological effects that are not always demonstrated by conventional bioassay-based monitoring.
机译:在1993年两次CEFAS研究航行期间,从英国的40多个河口,近岸和近海地点采集了水样。样品采用己烷萃取和浓缩程序进行处理,并使用海洋类拟立足类co足类Tisbe battagliai进行生物分析。此过程允许在所有位置测量非极性有机污染物的毒性作用,表示为引发48小时中值致命反应所需的浓度因子。还对总烃(THC)和多环芳烃(PAH)进行了定量,以估计它们对样品毒性的影响。在观察到毒性之前,对于河口场所,提取的污染物浓缩<10-300倍,对于近岸场所浓缩为<100-600倍,对于近海场所浓缩为<350-> 1000倍。研究河口的暂定水污染等级为:Tees> Wear> Mersey> Tyne> Blyth,普尔港,南安普敦Water> Ribble,Dee,Lune。化学分析表明,水中的总烃浓度与引起中等致死反应所需的浓度因子之间存在微弱但统计学上显着的相关性(-0.36至-0.43)。对照测定与藻类荧光和毒性之间没有相关性。结果表明,碳氢化合物可能对河口和沿岸水域的毒性做出重大潜在贡献,选定的10种PAH化合物估计在一个特定地点占总毒性的18%。然而,大多数毒性反应的原因仍然不确定。尽管该技术基于急性终点,但近海和近海站点所需的高浓度因子表明,未经处理的海水中不存在可长期萃取的己烷可萃取污染物。但是,在某些河口站点,低浓度因子(<200倍)表明这些水可能表现出慢性生物学作用,而常规基于生物测定的监测并不总是能证明这一点。

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