Protocol for the Derivation of Environmental and Human ... - CCME
Protocol for the Derivation of Environmental and Human ... - CCME
Protocol for the Derivation of Environmental and Human ... - CCME
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Part B, Section 2<br />
There is consistent use <strong>and</strong> acceptance <strong>of</strong> <strong>the</strong> 7 <strong>and</strong> 14 day mortality test as a short-term test <strong>for</strong><br />
earthworms (e.g., OECD, 1984a; Greene et al. 1989; ISO, 1991) <strong>and</strong> <strong>for</strong> <strong>the</strong> five-day seed<br />
germination/root elongation test as a short-term test <strong>for</strong> plants (e.g., U.S. EPA, 1982; Porcella, 1983;<br />
Ratsch <strong>and</strong> Johndro, 1986; Thomas <strong>and</strong> Cline, 1985; Miller et al., 1985; Wang, 1987; Wang <strong>and</strong><br />
Williams, 1988; ASTM, 1990a; ASTM, 1990b). However, short-term toxicological tests <strong>for</strong> o<strong>the</strong>r<br />
soil-dependent organisms (e.g., isopods) are still under development (NISRP, 1991; ISO, 1992).<br />
Long-term st<strong>and</strong>ardized toxicity test methods <strong>for</strong> earthworms have recently been developed <strong>and</strong> o<strong>the</strong>rs<br />
are currently being developed <strong>for</strong> isopods (ISO, 1992; NISRP, 1991). Usually, long-term exposure<br />
tests <strong>for</strong> soil-dwelling organisms include at least one reproduction stage (in <strong>the</strong> case <strong>of</strong> soil<br />
invertebrates), or one growth cycle (in <strong>the</strong> case <strong>of</strong> plants). Long-term tests have been proposed <strong>for</strong><br />
earthworms (five-week reproduction-ISO, 1991) <strong>and</strong> some plants {life cycle flowering (ASTM,<br />
1991)}, but <strong>the</strong>re is some uncertainty in <strong>the</strong> selection <strong>of</strong> proper endpoints <strong>and</strong> methodologies <strong>for</strong> <strong>the</strong>se<br />
tests (OECD, 1990).<br />
The acceptability <strong>of</strong> short- <strong>and</strong> long-term tests <strong>for</strong> general use in this protocol should be determined on<br />
a study-by-study basis using <strong>the</strong> in<strong>for</strong>mation cited above as a guide. Data from long-term studies are<br />
preferred <strong>for</strong> deriving soil quality guidelines. However, given <strong>the</strong> limited availability <strong>of</strong> such data, shortterm<br />
toxicity data may be accepted <strong>for</strong> guidelines derivation.<br />
2.4.2 Short- <strong>and</strong> Long-term Tests <strong>for</strong> Mammalian <strong>and</strong> Avian Species<br />
A considerable number <strong>of</strong> st<strong>and</strong>ardized toxicological tests have been carried out on traditional<br />
laboratory animals using different endpoints <strong>for</strong> various types <strong>of</strong> exposure. One <strong>of</strong> <strong>the</strong> most common<br />
toxicity tests is <strong>the</strong> LD 50 (i.e., <strong>the</strong> lethal dose which results in 50% mortality <strong>of</strong> <strong>the</strong> test population). This<br />
test is normally an acute exposure <strong>of</strong>ten involving a single administration <strong>of</strong> various chemical doses to<br />
laboratory animals followed by a 7 to 14 day examination <strong>of</strong> lethal effects (Klassen, 1986).<br />
Un<strong>for</strong>tunately, a st<strong>and</strong>ardized method <strong>for</strong> conducting toxicity tests <strong>for</strong> wildlife <strong>and</strong> livestock species are<br />
generally lacking, with <strong>the</strong> exception <strong>of</strong> <strong>the</strong> five-day dietary LC 50 test <strong>for</strong> avian species (Hill <strong>and</strong><br />
H<strong>of</strong>fman, 1984).<br />
Historically, in mammalian <strong>and</strong> avian subacute <strong>and</strong> chronic lethality tests, <strong>the</strong> number <strong>of</strong> dose regimes<br />
<strong>of</strong>ten do not provide sufficient in<strong>for</strong>mation to calculate a dose that results in a 50% response. Thus,<br />
endpoints <strong>for</strong> chronic exposures are <strong>of</strong>ten reported as <strong>the</strong> no observed (adverse) effect level<br />
(NO(A)EL) <strong>and</strong> <strong>the</strong> lowest observed (adverse) effect level (LO(A)EL). Chronic adverse effects<br />
endpoints can be related to reproduction, growth, or viability resulting from a continuous exposure over<br />
a significant portion <strong>of</strong> <strong>the</strong> organism's lifespan. Subchronic exposures normally involve <strong>the</strong> same<br />
endpoint as chronic exposures, but are conducted over a shorter time period.<br />
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