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Malathion:
Profile Excerpts from the Extension Toxicology
Network (Extoxnet)
(Extoxnet is a Pesticide Information Project of Cooperative
Extension Offices of Cornell University, Oregon State University,
the University of Idaho, and the University of California at Davis
and the Institute for Environmental Toxicology, Michigan State
University. Major support and funding was provided by the
USDA/Extension Service/National Agricultural Pesticide Impact
Assessment Program. EXTOXNET primary files maintained and archived
at Oregon State University)
Malathion
Trade and Other Names:
Malathion is also known as carbophos, maldison and mercaptothion.
Trade names for products containing malathion include Celthion,
Cythion, Dielathion, El 4049, Emmaton, Exathios, Fyfanon and
Hilthion, Karbofos and Maltox.
Regulatory
Status: Malathion is a
slightly toxic compound in EPA toxicity class III. Labels for
products containing it must carry the Signal Word CAUTION.
Malathion is a General Use Pesticide (GUP).
Chemical Class:
organophosphate
Introduction:
Malathion is a nonsystemic, wide-spectrum organophosphate
insecticide. It was one of the earliest organophosphate
insecticides developed (introduced in 1950). Malathion is suited
for the control of sucking and chewing insects on fruits and
vegetables, and is also used to control mosquitoes, flies,
household insects, animal parasites (ectoparasites), and head and
body lice. Malathion may also be found in formulations with many
other pesticides.
Toxicological Effects:
- Acute toxicity: Effects of malathion are
similar to those observed with other organophosphates, except
that larger doses are required to produce them [2,8]. It has
been reported that single doses of malathion may affect immune
system response [2]. Symptoms of acute exposure to
organophosphate or cholinesterase-inhibiting compounds may
include the following: numbness, tingling sensations,
incoordination, headache, dizziness, tremor, nausea, abdominal
cramps, sweating, blurred vision, difficulty breathing or
respiratory depression, and slow heartbeat. Very high doses may
result in unconsciousness, incontinence, and convulsions or
fatality. The acute effects of malathion depend on product
purity and the route of exposure [33]. Other factors which may
influence the observed toxicity of malathion include the amount
of protein in the diet and gender. As protein intake decreased,
malathion was increasingly toxic to the rats [78]. Malathion has
been shown to have different toxicities in male and female rats
and humans due to metabolism, storage, and excretion differences
between the sexes, with females being much more susceptible than
males [79]. Numerous malathion poisoning incidents have occurred
among pesticide workers and small children through accidental
exposure. In one reported case of malathion poisoning, an infant
exhibited severe signs of cholinesterase inhibition after
exposure to an aerosol bomb containing 0.5% malathion [44].
- Chronic toxicity: Weanling male rats
were twice as susceptible to malathion as adults.
- Reproductive effects: Several studies have
documented developmental and reproductive effects due to high
doses of malathion in test animals [2]. Rats fed high doses of
240 mg/kg/day during pregnancy showed an increased rate of
newborn mortality. However, malathion fed to rats at low dosages
caused no reproductive effects [8]. It is not likely that
malathion will cause reproductive effects in humans under normal
circumstances.
- Teratogenic effects: Rats fed high doses
(240 mg/kg/day) showed no teratogenic effects. Malathion and its
metabolites can cross the placenta of the goat and depress
cholinesterase activity of the fetus [8]. Chickens fed diets at
low doses for 2 years showed no adverse effects on egg hatching
[8]. Current evidence indicates that malathion is not
teratogenic.
- Mutagenic effects: Malathion produced
detectable mutations in three different types of cultured human
cells, including white blood cells and lymph cells [2,8]. It is
not clear what the implications of these results are for humans.
- Carcinogenic effects: Adrenal tumors
developed in the males at low doses, but not at the high doses
[80], suggesting that malathion was not the cause. Three of five
studies that have investigated the carcinogenicity of malathion
have found that the compound does not produce tumors in the test
animals. The two other studies have been determined to be
unacceptible studies and the results discounted [2,8,80].
Available evidence suggests that malathion is not carcinogenic
but the data are not conclusive.
- Organ toxicity: The pesticide has been
shown in animal testing and from use experience to affect the
central nervous system, immune system, adrenal glands, liver,
and blood.
- Fate in humans and animals: Malathion is
rapidly and effectively absorbed by practically all routes
including the gastrointestinal tract, skin, mucous membranes,
and lungs. Malathion undergoes similar detoxification mechanisms
to other organophosphates, but it can also be rendered nontoxic
via another simple mechanism, splitting of either of the carboxy
ester linkages. Most of the occupational evidence
indicates a low chronic toxicity for malathion. One important
exception to this was traced to impurities in the formulation of
the pesticide [2].
Ecological Effects:
- Effects on birds: Malathion is moderately
toxic to birds. The reported acute oral LD50 values are: in
mallards, 1485 mg/kg; in pheasants, 167 mg/kg; in blackbirds and
starlings, over 100 mg/kg; and in chickens, 525 mg/kg [2,6]. The
reported 5- to 8-day dietary LC50 is over 3000 ppm in Japanese
quail, mallard, and northern bobwhite, and is 2639 ppm in
ring-neck pheasants [6]. Furthermore, 90% of the dose to birds
was metabolized and excreted in 24 hours via urine [79].
- Effects on aquatic organisms: Malathion has
a wide range of toxicities in fish, extending from very highly
toxic in the walleye (96-hour LC50 of 0.06 mg/L) to highly toxic
in brown trout (0.1 mg/L) and the cutthroat trout (0.28 mg/L),
moderately toxic in fathead minnows (8.6 mg/L) and slightly
toxic in goldfish (10.7 mg/L) [13,8,16]. Various aquatic
invertebrates are extremely sensitive, with EC50 values from 1
ug/L to 1 mg/L [28]. Malathion is highly toxic to aquatic
invertebrates and to the aquatic stages of amphibians. Because
of its very short half-life, malathion is not expected to
bioconcentrate in aquatic organisms. However, brown shrimp
showed an average concentration of 869 and 959 times the ambient
water concentration in two separate samples [12].
- Effects on other organisms:
The compound is highly toxic to honeybees
[13].
Environmental Fate:
- Breakdown in soil and groundwater:
Malathion is of low persistence in soil with reported field
half-lives of 1 to 25 days [19]. Degradation in soil is rapid
and related to the degree of soil binding [12]. Breakdown occurs
by a combination of biological degradation and nonbiological
reaction with water [12]. If released to the atmosphere,
malathion will break down rapidly in sunlight, with a reported
half-life in air of about 1.5 days [12]. It is moderately bound
to soils, and is soluble in water, so it may pose a risk of
groundwater or surface water contamination in situations which
may be less conducive to breakdown. The
compound was detected in 12 of 3252 different groundwater
sources in two different states, and in small concentrations in
several wells in California, with a highest concentration of
6.17 ug/L [33].
- Breakdown in water: In raw river water, the
half-life is less than 1 week, whereas malathion remained stable
in distilled water for 3 weeks [12]. Applied at 1 to 6 lb/acre
in log ponds for mosquito control, it was effective for 2.5 to 6
weeks [12]. In sterile seawater, the degradation increases with
increased salinity. The breakdown products in water are mono-
and dicarboxylic acids [12].
- Breakdown in vegetation: Residues were
found mainly associated with areas of high lipid content in the
plant. Increased moisture content increased degradation [33].
Exposure Guidelines:
- ADI: 0.02 mg/kg/day [38]
- MCL: Not Available
- RfD: 0.02 mg/kg/day [53]
- PEL: 15 mg/m3 (8-hour) (dust) [39]
- HA: 0.2 mg/L (lifetime) [53]
- TLV: Not Available
References:
References for the information in this PIP can be found in
Reference List
Number 5
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