Results 171 to 180 of about 7,133 (224)
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Food and Cosmetics Toxicology, 1968
Abstract The body burden of HEOD is a reflection of the intensity of exposure to aldrin and dieldrin. While determination of HEOD in the blood is a satisfactory means of screening large groups for significant variations in degree of exposure, the more precise definition required for estimating body burdens in experimental subjects or in those exposed
C G, Hunter, J, Robinson
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Abstract The body burden of HEOD is a reflection of the intensity of exposure to aldrin and dieldrin. While determination of HEOD in the blood is a satisfactory means of screening large groups for significant variations in degree of exposure, the more precise definition required for estimating body burdens in experimental subjects or in those exposed
C G, Hunter, J, Robinson
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Pharmacodynamics of Dieldrin in Pigeons
International Journal of Pest Management: Part A, 1967CONSIDERABLE interest has been aroused in recent years by the presence of residues of organochlorine insecticides in the tissues of birds in Great Britain, and a comprehensive review of the situation up to 1965 has been made1. No information has been published yet on the pharmaco-dynamics of any of these compounds in birds.
J, Robinson, A, Richardson, V K, Brown
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Toxicity of Dieldrin and Endrin to Bats
Nature, 1965IN the course of our investigation of the storage and mobilization of lipids and pesticides in Chiroptera, it became necessary to obtain some data regarding the toxicity of various insecticides to bats. In a previous paper we reported that the big brown bat, Eptesicus fuscus, was extremely sensitive to DDT1.
M M, Luckens, W H, Davis
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Environment: Science and Policy for Sustainable Development, 1971
(1971). Aldrin and Dieldrin. Environment: Science and Policy for Sustainable Development: Vol. 13, No. 8, pp. 33-45.
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(1971). Aldrin and Dieldrin. Environment: Science and Policy for Sustainable Development: Vol. 13, No. 8, pp. 33-45.
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A Case of Fatal Dieldrin Poisoning
Medicine, Science and the Law, 1979Dieldrin was developed in the United States and was made available commercially in 1948. Chemically, dieldrin is 1, 2, 3, 4, 10, 10-hexachloro-6, 7-epoxy-1, 4, 4a, 5, 6, 7, 8, 8a-octahydro-1, 4, 5, 8-dimethanonaphthalene and forms, together with aldrin and endrin, a triumvirate of insecticides derived from hexachlorodicyclopentadiene. High insecticidal
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