Due to the large usage of DDT-containing antifouling paints and lindane in China, heavy residuals of DDTs and HCHs have been found in many fishing harbors, but there is lack of studies on this issue for the Zhanjiang ...Due to the large usage of DDT-containing antifouling paints and lindane in China, heavy residuals of DDTs and HCHs have been found in many fishing harbors, but there is lack of studies on this issue for the Zhanjiang Bay which is an important fishing harbor and mariculture zone in South China. To evaluate the pollution status and sources of HCHs and DDTs in the Zhanjiang Bay, the concentrations, spatial distributions and sources in the sediments of 11 land-based sewage outlets to the Zhanjiang Bay were investigated. Since the 1980 s, HCHs residuals had obviously decreased in studied areas, but DDTs had little change, even abnormally high levels were found in some sites. The content percentages and diagnostic ratios of HCHs isomers and DDTs showed that the source of HCHs was derived from soils around the bay and recent input of lindane, and DDTs were from historical residues of technical DDTs and fresh input of DDT-containing antifouling paints on fishing ships. Based on sediment quality guidelines, DDTs would be of more concern for the ecotoxicological risk on marine environment and adverse effects on benthonic organisms. This study indicated that lindane and DDT-containing products may be still used in some places of Zhanjiang City. It should be urgent to control their usage and clean the DDTs-contaminated sites by the local government.展开更多
The distribution of hexachloroeyclohexanes （HCHs） and dichlorodiphenyltrichloroethanes （DDTs） in the surface sea- water and sediment of Jincheng Bay mariculture area were investigated in the present study. The con...The distribution of hexachloroeyclohexanes （HCHs） and dichlorodiphenyltrichloroethanes （DDTs） in the surface sea- water and sediment of Jincheng Bay mariculture area were investigated in the present study. The concentration of total HCHs and DDTs ranged from 2.98 to 14.87ngL-l and were〈0.032ngL-1, respectively, in surface seawater, and ranged from 5.52 to 9.43 and from 4.11 to 6.72 ng g-l, respectively, in surface sediment. It was deduced from the composition profile of HCH isomers and DDT congeners that HCH residues derived from a mixture of technical-grade HCH and lindane whereas the DDT residues derived from technical-grade DDT and dicofol. Moreover, both HCH and DDT residues may mainly originate from historical inputs. The hazard quotient of α-HCH, β-HCH, γ-HCH and δ-HCH to marine species was 0.030, 0.157, 3.008 and 0.008, respectively. It was estimated that the overall probability of adverse biological effect from HCHs was less than 5%, indicating that its risk to seawater column spe- cies was low. The threshold effect concentration exceeding frequency of γ-HCH, p,p＇-DDD, p,p＇-DDE and p,p＇-DDT in sediment ranged from 8.3% to 100%, and the relative concentration of the HCH and DDT mixture exceeded their probable effect level in sediment. These findings indicated that the risk to marine benthos was high and potentially detrimental to the safety of aquatic prod- ucts, e.g., sea cucumber and benthic shellfish.展开更多
Three extraction techniques have been recently used for the quantitative extraction of semi-volatile organic pollutants in sediments, i.e. accelerated solvent extraction （ASE）, microwave assisted extraction （MAE） ...Three extraction techniques have been recently used for the quantitative extraction of semi-volatile organic pollutants in sediments, i.e. accelerated solvent extraction （ASE）, microwave assisted extraction （MAE） and ultrasonic assisted extraction （UAE）. However, their extraction efficiencies have rarely been quantitatively compared using rigorous mathematical methods. In this paper, one-way analysis of variance （ANOVA） was employed to evaluate the performance of ASE, MAE and UAE in the overall extraction of PCBs, DDTs and HCHs by analysis of their recoveries from the Standard Reference Material IAEA-417, a sediment sample certified by many international laboratories. Conclusions were drawn at a significance level of P〈 0.05. No significant differences were found among the mean values for method recoveries using ASE, MAE and UAE. The mean values for real recoveries using ASE and MAE were nearly identical, but the real recovery using UAE was much lower. The concentrations of all PCBs, DDTs and HCHs except for CB52 and o,p＇-DDT using UAE were the lowest. Comparing the results obtained using ASE with MAE, the concentrations of CB28, CB52, CB138, ct-HCH, [3-HCH, p,p＇-DDE and p,p＇-DDD were nearly identical, while the concentrations of other compounds were significantly different. Based on the low recoveries, it was concluded that UAE is a relatively inefficient extraction method, while ASE and MAE are equivalent methods. Taking into consideration the relative standard deviation （RSD） values, solvent volume, extraction time, and purchasing costs of the apparatus, MAE was considered superior to ASE for extraction of PCBs, DDTs and HCHs.展开更多
The spatial variability in the concentrations of 1,2,3,4,5,6-hexachlorocyclohexane （HCH） and 1,1,1-trichloro-2,2-bis-（p-chloro- phenyl） ethane （DDT） in surface soils was studied on the basis of the analysis of 1...The spatial variability in the concentrations of 1,2,3,4,5,6-hexachlorocyclohexane （HCH） and 1,1,1-trichloro-2,2-bis-（p-chloro- phenyl） ethane （DDT） in surface soils was studied on the basis of the analysis of 131 soil samples collected from the surface layer （0-20 cm depth） of the alluvial region of Beijing, China. The concentrations of total HCHs （including α-,β-, γ-, and δ-isomers） and total DDTs （including p,p＇-DDT, p,p＇-DDD, p,p＇-DDE, and o,p＇-DDT） in the surface soils tested were in the range from nondetectable to 31.72 μg/kg dry soil, with a mean value of 0.91, and from nondetectable to 5910.83 μg/kg dry soil, with a mean value of 32.13, respectively. It was observed that concentrations of HCHs in all soil samples and concentrations of DDTs in 112 soil samples were much lower than the first grade （50 μg/kg） permitted in ＂Environment quality standard for soils in China （GB 15618-1995）＂. This suggests that the pollution due to organochlorine pesticides was generally not significant in the farmland soils in the Beijing alluvial region. In this study, the spatial distribution and trend of HCHs and DDTs were analyzed using Geostatistical Analyst and GS＋（513）. Spatial distribution indicated how these pesticides had been applied in the past. Trend analysis showed that the concentrations of HCHs, DDTs, and their related metabolites followed an obvious distribution trend in the surface soils from the alluvial region of Beijing.展开更多
基金The International Scientific & Technological Cooperation Project of Department of Education of Guangdong Province,China under contract No.2015KGJHZ017the National Natural Science Foundation of China under contract Nos 41376125 and 41006070the “First-class” Special Funds of Guangdong Ocean University under contract No.231419018
文摘Due to the large usage of DDT-containing antifouling paints and lindane in China, heavy residuals of DDTs and HCHs have been found in many fishing harbors, but there is lack of studies on this issue for the Zhanjiang Bay which is an important fishing harbor and mariculture zone in South China. To evaluate the pollution status and sources of HCHs and DDTs in the Zhanjiang Bay, the concentrations, spatial distributions and sources in the sediments of 11 land-based sewage outlets to the Zhanjiang Bay were investigated. Since the 1980 s, HCHs residuals had obviously decreased in studied areas, but DDTs had little change, even abnormally high levels were found in some sites. The content percentages and diagnostic ratios of HCHs isomers and DDTs showed that the source of HCHs was derived from soils around the bay and recent input of lindane, and DDTs were from historical residues of technical DDTs and fresh input of DDT-containing antifouling paints on fishing ships. Based on sediment quality guidelines, DDTs would be of more concern for the ecotoxicological risk on marine environment and adverse effects on benthonic organisms. This study indicated that lindane and DDT-containing products may be still used in some places of Zhanjiang City. It should be urgent to control their usage and clean the DDTs-contaminated sites by the local government.
基金supported by the Marine Special Scientific Fund for the Non-profit Public Industry of China (200805031)Fund of Key Laboratory of Fishery Ecology and Environment, Guangdong Province (LFE-20144)Scientific Research Foundation for the Third Institute of Oceanography, State Oceanic Administration (No. 2013031)
文摘The distribution of hexachloroeyclohexanes （HCHs） and dichlorodiphenyltrichloroethanes （DDTs） in the surface sea- water and sediment of Jincheng Bay mariculture area were investigated in the present study. The concentration of total HCHs and DDTs ranged from 2.98 to 14.87ngL-l and were〈0.032ngL-1, respectively, in surface seawater, and ranged from 5.52 to 9.43 and from 4.11 to 6.72 ng g-l, respectively, in surface sediment. It was deduced from the composition profile of HCH isomers and DDT congeners that HCH residues derived from a mixture of technical-grade HCH and lindane whereas the DDT residues derived from technical-grade DDT and dicofol. Moreover, both HCH and DDT residues may mainly originate from historical inputs. The hazard quotient of α-HCH, β-HCH, γ-HCH and δ-HCH to marine species was 0.030, 0.157, 3.008 and 0.008, respectively. It was estimated that the overall probability of adverse biological effect from HCHs was less than 5%, indicating that its risk to seawater column spe- cies was low. The threshold effect concentration exceeding frequency of γ-HCH, p,p＇-DDD, p,p＇-DDE and p,p＇-DDT in sediment ranged from 8.3% to 100%, and the relative concentration of the HCH and DDT mixture exceeded their probable effect level in sediment. These findings indicated that the risk to marine benthos was high and potentially detrimental to the safety of aquatic prod- ucts, e.g., sea cucumber and benthic shellfish.
基金Supported by the National High Technology Research and Development Program of China (No. 2007AA09Z126)the Marine Science Foundation for Young Scholars of SOA (No. 2011519)Marine Commonwealth Scientific Support Fund of SOA (Nos. 201005034, 201105013)
文摘Three extraction techniques have been recently used for the quantitative extraction of semi-volatile organic pollutants in sediments, i.e. accelerated solvent extraction （ASE）, microwave assisted extraction （MAE） and ultrasonic assisted extraction （UAE）. However, their extraction efficiencies have rarely been quantitatively compared using rigorous mathematical methods. In this paper, one-way analysis of variance （ANOVA） was employed to evaluate the performance of ASE, MAE and UAE in the overall extraction of PCBs, DDTs and HCHs by analysis of their recoveries from the Standard Reference Material IAEA-417, a sediment sample certified by many international laboratories. Conclusions were drawn at a significance level of P〈 0.05. No significant differences were found among the mean values for method recoveries using ASE, MAE and UAE. The mean values for real recoveries using ASE and MAE were nearly identical, but the real recovery using UAE was much lower. The concentrations of all PCBs, DDTs and HCHs except for CB52 and o,p＇-DDT using UAE were the lowest. Comparing the results obtained using ASE with MAE, the concentrations of CB28, CB52, CB138, ct-HCH, [3-HCH, p,p＇-DDE and p,p＇-DDD were nearly identical, while the concentrations of other compounds were significantly different. Based on the low recoveries, it was concluded that UAE is a relatively inefficient extraction method, while ASE and MAE are equivalent methods. Taking into consideration the relative standard deviation （RSD） values, solvent volume, extraction time, and purchasing costs of the apparatus, MAE was considered superior to ASE for extraction of PCBs, DDTs and HCHs.
基金Project supported by the National Natural Science Foundation of China (No. 40201023)the Program for Changjiang Scholars and Innovative Research Team in University (IRT0412).
文摘The spatial variability in the concentrations of 1,2,3,4,5,6-hexachlorocyclohexane （HCH） and 1,1,1-trichloro-2,2-bis-（p-chloro- phenyl） ethane （DDT） in surface soils was studied on the basis of the analysis of 131 soil samples collected from the surface layer （0-20 cm depth） of the alluvial region of Beijing, China. The concentrations of total HCHs （including α-,β-, γ-, and δ-isomers） and total DDTs （including p,p＇-DDT, p,p＇-DDD, p,p＇-DDE, and o,p＇-DDT） in the surface soils tested were in the range from nondetectable to 31.72 μg/kg dry soil, with a mean value of 0.91, and from nondetectable to 5910.83 μg/kg dry soil, with a mean value of 32.13, respectively. It was observed that concentrations of HCHs in all soil samples and concentrations of DDTs in 112 soil samples were much lower than the first grade （50 μg/kg） permitted in ＂Environment quality standard for soils in China （GB 15618-1995）＂. This suggests that the pollution due to organochlorine pesticides was generally not significant in the farmland soils in the Beijing alluvial region. In this study, the spatial distribution and trend of HCHs and DDTs were analyzed using Geostatistical Analyst and GS＋（513）. Spatial distribution indicated how these pesticides had been applied in the past. Trend analysis showed that the concentrations of HCHs, DDTs, and their related metabolites followed an obvious distribution trend in the surface soils from the alluvial region of Beijing.
