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toxicological profile for malathion - Agency for Toxic Substances and ...

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MALATHION 187<br />

6.3.2.1 Air<br />

6. POTENTIAL FOR HUMAN EXPOSURE<br />

Pesticides may be trans<strong>for</strong>med <strong>and</strong> degraded in the atmosphere due to photolysis <strong>and</strong> by reaction with<br />

ozone, hydroxyl, <strong>and</strong> nitrate radicals. Very little definitive in<strong>for</strong>mation was found in the literature on the<br />

trans<strong>for</strong>mation <strong>and</strong> degradation of <strong>malathion</strong> in air. Bradman et al. (1994) stated that both <strong>malathion</strong> <strong>and</strong><br />

malaoxon are unstable in the atmosphere <strong>and</strong> that reported half-lives <strong>for</strong> the two compounds in air range<br />

from a few hours to 1 day; however, a review of the original papers cited in Bradman et al. (1994) do not<br />

directly support this statement <strong>for</strong> <strong>malathion</strong> <strong>and</strong> malaoxon specifically (Atkinson et al. 1989; Goodman<br />

et al. 1988). In a review paper, Mulla et al. (1981) stated that although the effects of light (including<br />

ultraviolet [UV] radiation) on both <strong>malathion</strong> <strong>and</strong> its degradate malaoxon have been studied, little is<br />

understood of the trans<strong>for</strong>mation of the parent to malaoxon through photolysis. Howard (1991) reported<br />

an estimated atmospheric photooxidation half-life of 1.5 days based on the reaction of <strong>malathion</strong> with<br />

photochemically produced hydroxy radicals. Based on the scarce data available in the literature, it<br />

appears that <strong>malathion</strong> degradation in the atmosphere occurs mainly due to indirect photolysis (photooxidation)<br />

rather than resulting from direct photolysis. In a photodegradation study of <strong>malathion</strong> exposed<br />

to natural sunlight <strong>and</strong> UV irradiation (maximum wavelength of 360 nm) as thin films on glass, the<br />

compound was relatively stable to sunlight <strong>and</strong> exhibited only slight degradation (16%) by 25 hours under<br />

UV light; none of the six degradates were present at >0.01% (Chukwudebe et al. 1989). In a non-U.S.<br />

study of <strong>malathion</strong> adsorbed to fly ash (particulate matter), Bossan et al. (1995) determined that adsorbed<br />

<strong>malathion</strong> is photodegraded when exposed to irradiation of >290 nm <strong>for</strong> up to 1.5 hours, but does not<br />

degrade when adsorbed to kaolin. Malathion on fly ash decreased by up to 70% of the adsorbed<br />

compound following 40 minutes of irradiation. However, the study authors attributed the degradation of<br />

<strong>malathion</strong> on fly ash to the presence of metals <strong>and</strong> metal oxides in the fly ash.<br />

6.3.2.2 Water<br />

Malathion in water undergoes chemical <strong>and</strong> microbial degradation. The rate <strong>and</strong> extent of its degradation<br />

is dependent on the chemical <strong>and</strong> physical properties of the water system, particularly temperature <strong>and</strong> the<br />

solution pH, in addition to the composition of the microbial population present in the system.<br />

Malathion is degraded rapidly by hydrolysis at more alkaline pH levels, but is stable to hydrolysis at<br />

acidic pHs (Wolfe et al. 1975, 1977). In a review paper, Mulla et al. (1981) noted that <strong>malathion</strong> was<br />

instantaneously degraded by hydrolysis at pH 12; had a half-life of approximately 1 day at pH 11; was

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