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Carbaryl, Carbofuran, and Methomyl - National Marine Fisheries ...

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(e.g., survival, growth, etc.). The information provided by EPA addressed aspects of survival,<br />

growth <strong>and</strong> reproduction of aquatic species (freshwater <strong>and</strong> saltwater), as well as providing some<br />

discussion on other information found in the open literature, such as results from some field<br />

experiments <strong>and</strong> experiments that evaluated sublethal effects. NMFS is charged under the ESA<br />

to evaluate all direct <strong>and</strong> indirect effects of an action. We therefore evaluate all aspects of an<br />

action that may reduce fitness of individuals or reduce primary constituent elements of<br />

designated critical habitat. The evaluation includes information that EPA provided on survival,<br />

growth, or reproduction, but also encompasses a broader range of endpoints including behaviors,<br />

endocrine disruption, <strong>and</strong> other physiological alterations. The information we assessed is<br />

derived from published, scientific journals <strong>and</strong> information from government agency reports,<br />

theses, books, information <strong>and</strong> data provided by the registrants identified as applicants, <strong>and</strong><br />

independent reports. Typically, the most relevant study results are those that directly measure<br />

effects to an identified assessment endpoint derived from experiments with salmonids, preferably<br />

listed Pacific salmonids or hatchery surrogates, exposed to the stressors of the action.<br />

Figure 37. Response analysis<br />

Mode <strong>and</strong> Mechanism of Action<br />

Effects of pesticide products on<br />

ESA-listed species <strong>and</strong> their habitat<br />

Individual<br />

responses<br />

Response Profile<br />

Habitat<br />

responses<br />

<strong>Carbaryl</strong>, carbofuran, <strong>and</strong> methomyl share a similar mode <strong>and</strong> mechanism of toxic action <strong>and</strong> are<br />

a part of a group known as N-methyl carbamates. All three have similar chemical structures <strong>and</strong><br />

act as neurotoxicants by impairing nerve cell transmission in vertebrates <strong>and</strong> invertebrates. They<br />

inhibit the enzyme AChE, which is present in cholinergic synapses. The normal function of<br />

AChE is to break down (hydrolyze) the neurotransmitter, acetylcholine, thereby serving as an<br />

“off-switch” for the electrochemical signal transmissions along nerve cells <strong>and</strong> neuromuscular<br />

junctions. AChE is prevalent in a variety of cell <strong>and</strong> organ types throughout the body of<br />

312

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