Effects of three common pesticides on survival, food consumption and midgut bacterial communities of adult workers Apis cerana and Apis mellifera

被引:39
作者
Yang, Yang [1 ]
Ma, Shilong [1 ,2 ]
Yan, Zhenxiong [3 ]
Liu, Feng [4 ]
Diao, Qingyun [1 ]
Dai, Pingli [1 ]
机构
[1] Chinese Acad Agr Sci, Inst Apicultural Res, Key Lab Pollinating Insect Biol Agr, Beijing 100093, Peoples R China
[2] Fujian Agr & Forestry Univ, Bee Acad, Fuzhou 350002, Peoples R China
[3] Beijing Agr Univ, Beijing 102206, Peoples R China
[4] Jiangxi Inst Apicultural Res, Nanchang 330201, Jiangxi, Peoples R China
基金
北京市自然科学基金;
关键词
Apis mellifera; Apis cerana; LC50; Acute toxicity; Chronic toxicity; HONEY-BEE; GUT MICROBIOME; IN-VITRO; TOXICITY; EXPOSURE; CONTAMINATION; POLLINATORS; DIMETHOATE; RESIDUES; HEALTH;
D O I
10.1016/j.envpol.2019.03.077
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The acute and chronic toxicity of 3 common pesticides, namely, amitraz, chlorpyrifos and dimethoate, were tested in Apis mellifera and Apis cerana. Acute oral toxicity LC50 values were calculated after 24 h of exposure to contaminated syrup, and chronic toxicity was tested after 15 days of exposure to 2 sublethal concentrations of pesticides. The toxicity of the tested pesticides to A. mellifera and A. cerana decreased in the order of dimethoate > chlorpyrifos > amitraz. A. mellifera was slightly more sensitive to chlorpyrifos and dimethoate than A. cerana, while A. cerana was more sensitive to amitraz than A. mellifera. Chronic toxicity tests showed that 1.0 mg/L dimethoate reduced the survival of the two bee species and the food consumption of A. mellifera, while 1.0 mg/L amitraz and 1.0 mg/L chlorpyrifos did not affect the survival or food consumption of the two bee species. The treatment of syrup with amitraz at a concentration equal to 1/10th of the LC50 value did not affect the survival of or diet consumption by A. mellifera and A. cerana; however, chlorpyrifos and dimethoate at concentrations equal to 1 /10th of their respective LC50 values affected the survival of A. cerana. Furthermore, intestinal bacterial communities were identified using high-throughput sequencing targeting the V3-V4 regions of the 16S rDNA gene. All major honey bee intestinal bacterial phyla, including Proteobacteria (62.84%), Firmicutes (34.04%), and Bacteroidetes (2.02%), were detected. There was a significant difference in the microbiota species richness of the two species after 15 days; however, after 30 days, no significant differences were found in the species diversity and richness between A. cerana and A. mellifera exposed to 1.0 mg/L amitraz and 1.0 mg/L chlorpyrifos. Overall, our results confirm that acute toxicity values are valuable for evaluating the chronic toxicity of these pesticides to honey bees. (C) 2019 Elsevier Ltd. All rights reserved.
引用
收藏
页码:860 / 867
页数:8
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