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<br />272 <br /> 1.0 <br /> 08 <br />m 0.6 <br />:::. <br />Q; 04 <br />:l: <br />0 <br />a.. <br /> 0.2 <br /> <br />C.S. CHARBONNEAU ET At. <br /> <br /> <br />S <br /> <br />10 1S 20 <br />Range of Means <br /> <br />2S <br /> <br />Fi~..I. Power curve of the ANOVA (N= 10, IX = 0.05), or the prob- <br />ability of detecting a statistically significant difference between the <br />~eans of the treatment levels (control and recommended applica- <br />tion rate) for enclosure test I. <br /> <br />duction in Diptera emergence over the period of pesticide ap- <br />plications. Emergence from the RAR and control followed <br />an almost identical pattern throughout the sampling period. <br />Enclosure tests 2, 3, and 4 did not demonstrate toxic ef- <br />fects of Yectobac-G on the benthic fauna at RAR or 5 x RAR <br />during 1990. There was no statistically detectable effect of <br />Vectobac-G on benthic organisms at the RAR or 5 x RAR <br />in enclosure test 2 (Table 3). Invertebrate densities did not <br />differ significantly (ANOVA p> 0.05) between treatments. <br />Because the power of the test was fairly low (power = 0.37), <br />it is difficult to conclude that there was no effect due to pes- <br />ticide application. Nevertheless, verification test 2, conducted <br />with enclosure test 2, confirms that Vectobac-G applied at <br />the two concentrations (RAR and 5 x RAR) affected mos- <br />quito larvae (1000/0 mortality) (Table 3). <br /> <br /> 60 <br /> 50 <br />'" <br />c c Treatment <br />tV <br />Q; 40 ----11--- Control <br />a.. <br />'6 <br />'0 30 <br />t'? <br />Ql <br />.D <br />E 20 <br />=> <br />c <br />C <br />tV 10 <br />Ql <br />;:;: <br /> <br />o <br /> <br /> <br /> <br />mo~mo~mO~mQM~QN~M <br />-----NNM----__NN_ <br />~_______wmm-____~ <br />."."."."."."." CD CD CD CD CD <br /> <br />Date <br /> <br />Fig. 2. Mean number of adult dipterans (10 samples per treatment) <br />c~lIec!ed on emergence traps during enclosure test I, following ap- <br />pl.'catlons of Veclobac-G@) on May 10. May 25, and June 22, 1989, <br />~Iltle Bass Pond, Minnesota Valley National Wildlife Refuge, Bloom- <br />Ington, Minnesota. <br /> <br />30 <br /> <br />There were no reductions in the densities of Hyalella <br />azteca or Chironomidae in the treatments of enclosure test 3 <br />(Table 4). Mean densities remained less than one per sample <br />for H. azteca, and actually increased slightly in each treatment <br />for the chironomids. At 5 x RAR, Yectobac-G significantly <br />reduced Oligochaeta densities by about 50%. Verification test <br />3 validated the potency of Yectobac-G on mosquito larvae <br />in enclosure test 3 with 100% mortality at the RAR and 5 x <br />RAR (Table 4). <br />The natural temporal reduction in densities of chirono- <br />mids that was observed the first field season occurred again <br />during the second field season (Tables 3 and 4); therefore, <br />the enclosures were moved to where densities of chironomids <br />were greater. There were no significant statistical differences <br />due to treatment for any of the organisms in enclosure test <br />4 (Table 5). However, the likelihood of determining if <br />Yectobac-G affected benthic organisms was low (power = <br />0.06). In verification test 4, conducted for enclosure test 4, <br />there was 97 and 100% mortality of the mosquito larvae in <br />the two treatment levels of RAR and 5 x RAR, respectively <br />(Table 5). The pattern resulting from the four field tests was <br />clear. Applications were sufficient to completely eliminate <br />mosquitoes but had little detectable effect on the other com- <br />ponents of the benthic community. <br />Toxicity tests. Static acute tests were conducted to deter- <br />mine if chironomid larvae found in the field could be affected <br />by Yectobac-G under controlled conditions. Higher mortal- <br />ity of chironomids was evident at RAR for two tests and at <br />the elevated concentration of 5 x RAR in four of the five <br />tests (Table 6). In static test I, there was 100% mortality of <br />the mosquito larvae (Psorosphera spp.). Chironomid (Mi- <br />cropsectra [Tanytarsus) spp.) larvae exhibited low mortal- <br />ity in the control (27%) but high mortality-87% (RAR), <br />100% (2 x RAR), and 100% (5 x RAR)-in the three <br />treatments. <br />Although mortality at the RAR approached 50% in static <br />test 2, it was not much greater than the control (40%). There <br />was substantially greater mortality at 5 x RAR (93%). <br />No indication of an effect of Vectobac-G on the chi ron- <br />omid larvae tested in static test 3 was evident. Percentage of <br />mortality at RAR was the same as the control (27%) and was <br />lower than the control at 5 x RAR (23%). <br />Static test 4 demonstrated an effect on chironomid larvae <br />with 17% mortality at the RAR and 57% mortality at 5 x <br />RAR relative to control mortality of 0%. <br />Mosquito (Culex spp.) larvae tested in static test 5 exhib- <br />ited high mortality in both treatments of RAR and 5 x RAR <br />(97%). Chironomids were affected (43% mortality) only at <br />5 x RAR. In summary, chironomids were affected more se- <br />verely in laboratory toxicity tests compared to enclosure tests. <br />The following series of laboratory toxicity tests were used to <br />evaluate potential factors important in mitigating the toxic- <br />ity of Vectobac-G to chironomids in the field. <br /> <br />Laboratory toxicity tests <br /> <br />Range tests. The EC50 concentrations for Yectobac-G in <br />overlying water to C. riparius fell within the range of 0.08 <br />to 0.51 ppm. The toxicity of Yectobac-G was less toxic to chi- <br />