Abstract

Since the late 1970's flow cytometry has been accepted as a fast and accurate technique for the quantification of nuclear DNA content (Deaven 1982). However, use of the technology has typically been confined to clinical settings due to the high cost of the instrumentation and the requirement for trained personnel. Flow cytometry recently has been applied to the study of genetic damage in wild populations. McBee and Bickham (1988) detected DNA damage in wild rodents inhabiting a dumpsite contaminated with petrochemicals, and Bickham et al. (1988) detected DNA aneuploidy in turtles found in seepage basins contaminated with radiation. Given these few studies, there is a need to establish a data base for the application of flow cytometry to environmental screening.

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