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

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<strong>Carbaryl</strong> dissipates in the environment by abiotic <strong>and</strong> microbially mediated degradation.<br />

The environmental fate characteristics for carbaryl are listed below (Table 44).<br />

Table 44. Environmental fate characteristics of carbaryl (EPA 2003).<br />

Parameter Value<br />

Water solubility 32 mg/L at 20 deg C<br />

Vapor pressure 1.36 10-7 torrs<br />

Henry's law constant 1.28 x 10-8 atm m3 /mol<br />

Octanol/Water partition Kow = 229<br />

Hydrolysis (t1/2) pH 5, pH 7, <strong>and</strong> pH 9 Stable, 12 days, 3.2 hours<br />

Aqueous photolysis (t½) 21 days<br />

Soil photolysis(t½) assumed stable<br />

Aerobic soil metabolism (t½) 4 days - s<strong>and</strong>y loam soil<br />

Anaerobic soil metabolism (t½) 72 days<br />

Aerobic aquatic metabolism (t½) 4.9 days<br />

Anaerobic aquatic metabolism (t½) 72 days<br />

Koc<br />

177- 249 ml/g<br />

Fish are most likely to be exposed to carbaryl through direct uptake of the chemical from<br />

the water column <strong>and</strong> across the gills, although other routes of exposure may also be<br />

important. Potential exposure routes for aquatic organisms include direct uptake from the<br />

water column or pore water of sediment, incidental ingestion of the chemical in sediment,<br />

or ingestion of the chemical in food items. EPA asserts that “carbaryl is not expected to<br />

bioaccumulate” <strong>and</strong> reports a bioacculation factor of 45 (EPA 2003). Other sources<br />

suggest accumulation of carbaryl can occur in fish, invertebrates, algae <strong>and</strong> plants.<br />

Residue levels in fish can be 140 fold greater than the concentration of carbaryl in water<br />

(http://pmep.cce.cornell.edu/profiles/extoxnet/carbaryl-dicrotophos/carbaryl-<br />

ext.html#14). In general, due to its rapid metabolism <strong>and</strong> rapid degradation, carbaryl<br />

should not pose a significant bioaccumulation risk in alkaline waters. However, under<br />

conditions below neutrality accumulation of carbaryl may be significant<br />

(http://pmep.cce.cornell.edu/profiles/extoxnet/carbaryl-dicrotophos/carbaryl-<br />

ext.html#14).<br />

EPA reports the major degradation products of carbaryl are CO2 <strong>and</strong> 1-naphthol, which is<br />

further degraded to CO2 (EPA 2003). <strong>Carbaryl</strong> is stable to hydrolysis in acidic conditions<br />

but hydrolyzes in neutral environments. Hydrolysis rates increase with increasing<br />

alkalinity. <strong>Carbaryl</strong> is degraded by photolysis in water with a half-life of 21 days (d).<br />

269

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