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homologous series, that diorganotins are less toxic than the corresponding <br />triorganotins (Table 8). It was concluded that the toxicity of organotins to <br />crab zoeae seems to be a function of the hydrophobic characteristics conferred <br />by the number and structure of the organic ligands (Laughlin et al. 1985). <br />Signs of tributyltin poisoning in rainbow trout and other freshwater <br />teleosts include sluggishness; loss of appetite; altered body pigmentation; <br />air gulping; loss of positive rheotaxis; increased rate of opercular <br />movements; damaged gills, cornea, and epithelial cells of bile duct; and <br />increases in blood hemoglobin, erythrocyte number, and hematocrit <br />(Chliamovitch and Kuhn 1977; Thompson et al. 1985). These changes were <br />consistent with the known inhibitory effects on mitochondrial and oxidative <br />phosphorylation of triorganotin compounds. Suppression of regeneration in <br />echinoderms, and presumably other aquatic groups, may be due primarily to <br />neurotoxicological action of organotins, or secondarily by direct action on <br />tissue at the breakage point (Walsh et al. 1986b). <br />Studies on lethal and sublethal effects of tin compounds to <br />representative species of aquatic organisms demonstrate that organotin <br />compounds are more toxic than inorganic tin compounds; triorganotin compounds <br />are more toxic than mono-, di-, or tetraorgano forms; and tributyltin <br />compounds are the most toxic triorganotin compounds tested (Table 9). Adverse <br />effects of tributyltins were noted at water concentrations of 0.001 to 0.06 <br />ug/l in marine gastropod and bivalve molluscs and at 0.1 to 1 ug/l in algae, <br />echinoderms, fish, crustaceans, and coelenterates (Table 9). In order of <br />toxicity, tributyltins were followed by tripropyltins (harmful effects <br />recorded at 0.001 to 10 ug/l to gastropods, fish, and algae), tripeenyltins <br />(0.6 to 1 ug/l to diatoms and annelids), triethyltins (3.8 to 10 ug/l to fish <br />and algae), trimethyltins (20 ug/l to algae and crustaceans), and <br />tripentyltins (50 to 100 ug/l to gastropods). Because many organotin <br />compounds are slow-acting poisons, short-term toxicity tests seriously <br />underestimate the toxicity of these compounds (Laughlin and Linden 1985). <br />Biological factors known to modify lethal and sublethal effects of <br />organotins include age of the organism, inherent interspecies resistance, and <br />tissue specificity. Abiotic modifiers include exposure route, and <br />physicochemical regimen. Early developmental stages were more sensitive to <br />organotins than later developmental stages in marine annelids (Walsh et al. <br />1986a), mysid shrimp (Hall and Pinkney 1985), and rainbow trout (Thompson et <br />al. 1985). Mortality of zoeae of fiddler crabs (Uca pugilator) to <br />trimethyltins was greatest at elevated temperatures and low salinities <br />(Thompson et al. 1985). Mussels expused through a diet of algae showed slow <br />accumulation of organotins when compared to exposure from the medium; the <br />reverse was observed for crabs (Evans and Laughlin 1984; Hall and Pinkney <br />1985; Laughlin et al. 1986a). A marine diatom (Thalassiosira pseudonana) <br />37