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from use of the pesticide are also determined. The Acute dermal (on skin) toxicity studies
benefits are weighed against the risks. When the Acute inhalation (breathing) toxicity studies on rats
benefits outweigh the risks, pesticide use is Primary eye irritation studies on rabbits
approved at application rates that will not create Primary dermal irritation studies on rabbits
unsafe residues. When the risks outweigh the
Dermal sensitization studies
benefits, use of the pesticide is either banned or
Acute delayed neurotoxicity (nerve) studies on hens
canceled.
Pesticides from raw products that carry over 90-day feeding studies on rodents and non-rodents
into processed food are considered food additives Chronic (long-term) feeding studies on rodents and non-
and are regulated by the 1958 Food Additives rodents
Amendment. This amendment differs from that Oncogenicity (tumor) studies on rats and mice
used to regulate pesticides on raw products in that Teratogenicity (birth defects) studies on two species
benefits are not considered if a possible risk of Two-generation mutagenicity (chromosome defects) tests
cancer is detected. According to the “Delaney
Gene mutation tests
Clause” of this amendment, no additive shall be
deemed to be safe if it is found to induce cancer Structural chromosomal aberration tests
Source
Joseph D. Waldrum, Director of Staff and Leadership Development,
Pamela L. Brady, Extension Foods Specialist, and
J. Ples Spradley, Extension Pesticide Impact Assessment Specialist,
Arkansas Cooperative Extension Service
Acknowledgments
This publication was developed under a project of the Southern Extension and Research Activity-
Information Exchange Group 1 (Southern Region Pesticide Impact Assessment Program). Partial Funding
for the publication was provided by U.S. Department of Agriculture Extension Service National Agricul-
tural Pesticide Impact Assessment Program special project 93-EPIX-1-145.