Genotoxicity of industrial wastes and effluents

被引:202
作者
Claxton, LD [1 ]
Houk, VS [1 ]
Hughes, TJ [1 ]
机构
[1] US EPA, Natl Hlth & Environm Effects Res Lab MD68, Res Triangle Pk, NC 27711 USA
关键词
complex mixture; risk analysis; pollutant; carcinogen; genotoxicity; remediation; Toxics Release Inventory (TRI); industrial effluent; Salmonella;
D O I
10.1016/S1383-5742(98)00008-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
In excess of several million pounds of genotoxic and/or carcinogenic industrial wastes are released into the U.S. environment each year. Chemical characterization of these waste materials can rarely provide an adequate assessment of their genotoxicity and potential hazard. Bioassays do not require prior information about chemical composition and can effectively assess the genotoxicity of complex waste materials. The most commonly used genotoxicity assay has been the Salmonella mutagenicity assay. Results with this system have shown that the genotoxic potency of industrial wastes can vary over 10 orders of magnitude, from virtually nondetectable to highly potent. Industries employing similar industrial processes generally release wastes of similar potency. Extremely high potency wastes include those from furazolidone and nitrofurfural production. Pulp and paper mills, steel foundries, and organic chemical manufacturing facilities also discharge wastes of noteworthy potency. Treatment and remediation of some wastes, such as pulp and paper mill effluents, have been shown to reduce or eliminate genotoxicity. However, in other cases, treatment and remediation have been shown to enhance genotoxicity, such as for fungal treatment of oils. Analyses of samples collected from areas known to receive industrial wastes and effluents have shown that genotoxins can accumulate in the receiving environment and have adverse effects on indigenous biota. The evaluation of hazardous wastes and effluents by genotoxicity assays may provide data useful not only for hazard identification but for comparative risk assessment. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:237 / 243
页数:7
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