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Effects of injudicious use of spirotetramat on Encarsia formosa's ability to control Bemisia tabaci.
Yang, Shao-Wu; Zhang, Bo; Tian, Ye; Peng, Lu; Yuan, Guo-Ting; Chen, Guo-Hua; Zhang, Xiao-Ming.
Affiliation
  • Yang SW; State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China; Yunnan Urban Agricultural Engineering and Technological Research Center, College of Agronomy and Life Sciences, Kunming University, Ku
  • Zhang B; State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China.
  • Tian Y; State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China.
  • Peng L; State Key Laboratory of Ecological Pest Control for Fujian-Taiwan Crops, Institute of Applied Ecology, Fujian Agriculture and Forestry University, Fuzhou 350002, China.
  • Yuan GT; State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China.
  • Chen GH; State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China.
  • Zhang XM; State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, College of Plant Protection, Yunnan Agricultural University, Kunming 650201, China.
Sci Total Environ ; 950: 175324, 2024 Nov 10.
Article in En | MEDLINE | ID: mdl-39127202
ABSTRACT
The excessive and frequent use of insecticides has led to serious problems with insecticide residues, impacting nontarget organisms such as the parasitoid Encarsia formosa. This study examined the growth, development, and enzyme activity of E. formosa exposed to spirotetramat at LC10, LC30, and LC50. The regression equation for the toxicity of spirotetramat toward E. formosa was Y = 5.25X-11.07. After exposure to spirotetramat, the survival rates of E. formosa sharply decreased, which occurred earlier than those in the control batch. Although the maximum daily parasitism quantity of E. formosa increased and the average parasitism number, enumerated from the 1st to the 5th day, was 53.97 after being exposed to spirotetramat at LC10, the life span of its F1 generation adults was only 8.47 days, which was significantly shorter than that in the control batch. After being exposed to spirotetramat at LC50, the average parasitism number of E. formosa was 63.30, and the developmental time of its F1 generation, enumerated from the 1st to the 5th day after exposure to spirotetramat, was significantly longer than that of the control batch. The activities of mixed function oxidase, acetylcholinesterase, carboxylesterase, and catalase increased significantly, and the rate of increase in enzyme activity was directly proportional to the increase in the concentration of spirotetramat. These results revealed that the parasitic ability of E. formosa decreased after exposure to spirotetramat at LC10, LC30, and LC50. This leads to a change in parasitoid control of pests, revealing the potential environmental threat of insecticide residues to nontarget organisms.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spiro Compounds / Aza Compounds / Wasps / Hemiptera / Insecticides Limits: Animals Language: En Journal: Sci Total Environ Year: 2024 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spiro Compounds / Aza Compounds / Wasps / Hemiptera / Insecticides Limits: Animals Language: En Journal: Sci Total Environ Year: 2024 Document type: Article Country of publication: