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Impact of - IDL-BNC @ IDRC - International Development Research ...

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On the basis <strong>of</strong> data compiled for a variety <strong>of</strong> pesticides, Tucker and Leitzke<br />

(1979) suggested that, in 95% <strong>of</strong> the cases, if the acute toxic dose <strong>of</strong> any given<br />

compound is known for one species <strong>of</strong> bird, then the acute toxic dose <strong>of</strong> the<br />

same compound will be within a factor <strong>of</strong> 10 (plus or minus) for a second<br />

species. However, one must be careful <strong>of</strong> such generalizations. Reanalysis <strong>of</strong><br />

part <strong>of</strong> the same data base (bird toxicity data for 44 organophosphate insecticides)<br />

determined that the range in acute toxicity values between species was<br />

highly dependant on, and therefore an artefact <strong>of</strong>, the number <strong>of</strong> species tested.<br />

The average number <strong>of</strong> species tested was 3.9 for compounds showing a range<br />

<strong>of</strong> toxicity less than one order <strong>of</strong> magnitude; those showing larger variation<br />

were tested on an average <strong>of</strong> 6.8 species.<br />

It has been argued (Schafer and Brunton 1979) that some species appear to<br />

show an inherent susceptibility or resistance to a wide range <strong>of</strong> environmental<br />

toxicants. Thus, current US regulatory testing using the Mallard (Arias<br />

platyrhynchos) and Bobwhite Quail (Colinus virginianus) should be revised,<br />

because these species do not give a realistic assessment <strong>of</strong> the hazards <strong>of</strong><br />

pesticides to the largest group <strong>of</strong> bird species, the passerines or perching birds.<br />

A reanalysis <strong>of</strong> some <strong>of</strong> the large data bases on acute toxicity <strong>of</strong> pesticides to<br />

birds (Schafer and Brunton 1979; Tucker and Leitzke 1979) has shown that<br />

phylogenetically related birds are not necessarily similarly sensitive to any<br />

given pesticide (Mineau 1991). This casts doubt on our ability to predict the<br />

hazard to a species on the basis <strong>of</strong> that in a closely related species. This type<br />

<strong>of</strong> extrapolation has been especially common in dealing with rare or endangered<br />

species or with species that are not amenable to direct investigation.<br />

Assessing dietary exposure<br />

Knowing which nontarget species are likely to be exposed during pesticide<br />

applications requires an understanding <strong>of</strong> exposure routes. Ingestion <strong>of</strong> contaminated<br />

food has been identified as the most likely route <strong>of</strong> intoxication for<br />

wild birds or mammals and is still the only route that is commonly assessed<br />

in standardized hazard-assessment procedures. However, the dietary route<br />

may not be the only or even the main route in all cases <strong>of</strong> wildlife exposure<br />

(Mineau et al. 1990).<br />

The food intake <strong>of</strong> a small organism is greater than that <strong>of</strong> a larger one when<br />

expressed asa ratio <strong>of</strong> body weight. Thus, other things being constant, smaller<br />

species tend to be more vulnerable to acute pesticide intoxication. Also, at<br />

certain times <strong>of</strong> the year, wildlife species may have higher energy requirements,<br />

and hence higher food intakes, than at other times. For example, a bird<br />

feeding young at the nest may have much higher energy requirements than<br />

normal. Climatic conditions and physical factors, such as nutritional status,<br />

disease, and parasite load also influence the toxicity <strong>of</strong> pesticides to the<br />

organism directly, whereas, indirectly, they may alter food consumption patterns<br />

causing the organism to ingest more or less <strong>of</strong> the pesticide.<br />

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