Volume 19, Issue 4 pp. 636-638
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Mirex and Aroclor® 1254: Effect on and Accumulation by Tetrahymena pyriformis Strain W*

NELSON R. COOLEY

NELSON R. COOLEY

Environmental Protection Agency, Gulf Breeze Laboratory, Sabine Island, Gulf Breeze, Fla. 32561 Associate Laboratory of the National Environmental Research Center, Corvallis, Oregon

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JAMES M. KELTNER JR.

JAMES M. KELTNER JR.

Environmental Protection Agency, Gulf Breeze Laboratory, Sabine Island, Gulf Breeze, Fla. 32561 Associate Laboratory of the National Environmental Research Center, Corvallis, Oregon

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JERROLD FORESTER

JERROLD FORESTER

Environmental Protection Agency, Gulf Breeze Laboratory, Sabine Island, Gulf Breeze, Fla. 32561 Associate Laboratory of the National Environmental Research Center, Corvallis, Oregon

We thank Dr. John O. Corliss for the initial cultures of T. pyriformis strain W from which our stock was derived, Allied Chemical Corporation for the sample of technical Mirex and the Monsanto Company for the sample of Aroclor 1254 used in this investigation, and David J. Hansen for valuable advice on the statistical analysis of our data.

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First published: November 1972
Citations: 34

Registered Trademark, Monsanto Co., St. Louis, Mo.

Contribution No. 137, Gulf Breeze Laboratory.

SYNOPSIS

Effects of 2 toxicants, Mirex and Aroclor 1254, on Tetrahymena pyriformis strain W in axenic cultures were investigated. Mirex is a chlorinated hydrocarbon effective against the fire ant, and Aroclor 1254 is a compound structurally related to DDT and used extensively in various industrial processes. Both toxicants reduced growth rates and population densities of T. pyriformis grown at 26 C generally in proportion to concentrations of the chemicals, their effects becoming statistically significant (P < 0.05) at 0.9 μg/liter for Mirex and 1.0 and 10.0 μg/liter for Aroclor 1254. Ciliates exposed to the toxicants for 7 days concentrated Mirex 193 × and Aroclor 60 × as compared to the initial concentrations of these compounds. It is suggested that the chief effect of the 2 toxicants on populations of T. pyriformis and of similarly responding ciliates in nature would be to reduce the availability of these protozoa as food organisms and nutrient regenerators. The ability of the ciliates to concentrate the tested compounds would permit the toxicants to enter into and to be translocated through aquatic food chains. In this manner the compounds could exert toxic effects at higher trophic levels.

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