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转基因棉花连续种植对土壤AM真菌群落结构的影响
引用本文:刘瑞华,陈静怡,王丽丽,李静,刘惠芬,杨殿林,赵建宁. 转基因棉花连续种植对土壤AM真菌群落结构的影响[J]. 农业环境科学学报, 2019, 38(2): 383-393
作者姓名:刘瑞华  陈静怡  王丽丽  李静  刘惠芬  杨殿林  赵建宁
作者单位:天津农学院农学与资源环境学院, 天津 300384;农业农村部环境保护科研监测所, 天津 300191;农业部产地环境污染防控重点实验室/天津市农业环境与农产品安全重点实验室, 天津 300191,天津农学院农学与资源环境学院, 天津 300384;农业农村部环境保护科研监测所, 天津 300191;农业部产地环境污染防控重点实验室/天津市农业环境与农产品安全重点实验室, 天津 300191,农业农村部环境保护科研监测所, 天津 300191;农业部产地环境污染防控重点实验室/天津市农业环境与农产品安全重点实验室, 天津 300191,农业农村部环境保护科研监测所, 天津 300191;东北农业大学资源与环境学院, 哈尔滨 150030;农业部产地环境污染防控重点实验室/天津市农业环境与农产品安全重点实验室, 天津 300191,天津农学院农学与资源环境学院, 天津 300384,农业农村部环境保护科研监测所, 天津 300191;农业部产地环境污染防控重点实验室/天津市农业环境与农产品安全重点实验室, 天津 300191,农业农村部环境保护科研监测所, 天津 300191;农业部产地环境污染防控重点实验室/天津市农业环境与农产品安全重点实验室, 天津 300191
基金项目:国家转基因重大专项(2016ZX08012005-005);中国农业科学院协同创新任务(CAAS-XTCX2016015)
摘    要:为评价转基因棉花种植对土壤中AM真菌群落结构的影响,以转基因棉花013011(抗旱)、SGK321(抗虫)和非转基因棉花TH2(抗旱受体)、石远321(抗虫受体)为材料,研究不同生育期转基因棉花土壤中AM真菌的群落结构。采用PCR-DGGE技术对土壤中AM真菌的群落结构进行分析。结果发现:转基因棉花与非转基因棉花在花铃期和吐絮期土壤中AM真菌群落的最小相似度均大于0.6,这说明了转基因棉花的种植在花铃期和吐絮期均未对土壤中AM真菌的群落结构产生影响。另外转基因棉花和非转基因棉花的种植在花铃期和吐絮期均未对土壤AM真菌的丰富度(S)造成影响;土壤AM真菌香农-维纳指数(H)仅在吐絮期石远321显著低于SGK321,其余品种和时期均未出现显著性差异;土壤AM真菌的均匀度(EH)仅在吐絮期发现TH2显著高于013011,其余品种和时期均未出现显著性差异。DGGE指纹图谱结果表明转基因棉花与非转基因棉花同一生长时期多为共有条带,且同一时期土壤AM真菌群落结构相似性较高,AM真菌的群落结构无明显变化。两个不同生育期优势属均为Glomus(球囊霉属)。研究表明:土壤AM真菌的群落结构变化只随着棉花生育期的不同会有短暂的变化,与是否为转基因棉花无显著性相关。

关 键 词:AM真菌  转基因棉花  PCR-DGGE
收稿时间:2018-03-20
修稿时间:2018-07-09

Effects of continuous planting of transgenic cotton on the community structure of AM fungi in soil
LIU Rui-hu,CHEN Jing-yi,WANG Li-li,LI Jing,LIU Hui-fen,YANG Dian-lin and ZHAO Jian-ning. Effects of continuous planting of transgenic cotton on the community structure of AM fungi in soil[J]. Journal of Agro-Environment Science( J. Agro-Environ. Sci.), 2019, 38(2): 383-393
Authors:LIU Rui-hu  CHEN Jing-yi  WANG Li-li  LI Jing  LIU Hui-fen  YANG Dian-lin  ZHAO Jian-ning
Affiliation:College of Agronomy & Resources and Environment, Tianjin Agricultural University, Tianjin 300384, China;Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, China;Key Laboratory of Original Agro-Environmental Pollution Prevention and Control, Ministry of Agriculture/Tianjin Key Laboratory of Agro-environment and Safe-product, Tianjin 300191, China,College of Agronomy & Resources and Environment, Tianjin Agricultural University, Tianjin 300384, China;Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, China;Key Laboratory of Original Agro-Environmental Pollution Prevention and Control, Ministry of Agriculture/Tianjin Key Laboratory of Agro-environment and Safe-product, Tianjin 300191, China,Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, China;Key Laboratory of Original Agro-Environmental Pollution Prevention and Control, Ministry of Agriculture/Tianjin Key Laboratory of Agro-environment and Safe-product, Tianjin 300191, China,Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, China;College of Resources and Environment, Northeast Agricultural University, Harbin, 150030, China;Key Laboratory of Original Agro-Environmental Pollution Prevention and Control, Ministry of Agriculture/Tianjin Key Laboratory of Agro-environment and Safe-product, Tianjin 300191, China,College of Agronomy & Resources and Environment, Tianjin Agricultural University, Tianjin 300384, China,Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, China;Key Laboratory of Original Agro-Environmental Pollution Prevention and Control, Ministry of Agriculture/Tianjin Key Laboratory of Agro-environment and Safe-product, Tianjin 300191, China and Agro-Environmental Protection Institute, Ministry of Agriculture and Rural Affairs, Tianjin 300191, China;Key Laboratory of Original Agro-Environmental Pollution Prevention and Control, Ministry of Agriculture/Tianjin Key Laboratory of Agro-environment and Safe-product, Tianjin 300191, China
Abstract:To detect the effects of cultivating transgenic crops on the community composition of soil arbuscular mycorrhizal (AM)fungi, we employed two transgenic cotton varieties, 013011 (drought-resistant)and SGK321 (insect-resistant), and their parental varieties TH2 (drought-resistant receptor)and Shiyuan321 (insect-resistant receptor). The Polymerase chain reaction-Denaturing gradient gel electrophoresis (PCR-DGGE)technology was used to analyze the community structure of the AM fungi in the soil. The results showed that the minimum similarity of the AM fungi in the soil with planted transgenic cotton and non-transgenic cotton was 0.6, indicating that the transgenic cotton planting had no significant effect on the community structure of the AM fungi in the soil during the blooming and the wadding stages. No significant difference in the richness (S)of the AM fungi was found between the soils planted with the transgenic and non-transgenic cotton during the blooming and wadding stages. The Shannon-Wiener index (H)of the AM fungi in the soil planted with Shiyuan 321 was significantly lower than that planted with SGK321 only at the wadding stage, However, no significant difference found among the other growing periods and other cotton types. The evenness (EH)of the AM fungi in the soil planted with TH2 was significantly higher than that planted with 013011 only at the wadding stage, but no significant difference was observed among the other cotton types and growing periods. The DGGE fingerprinting of the AM fungi in soil planted with the transgenic cotton was very similar to that planted with the non-transgenic cotton at the same growing stage, indicating that the impacts of planting the transgenic cotton on the community structure of the AM fungi in soil was small. The predominant genera were Glomus during both the flowering and boll-setting periods. The community structure of the AM fungi in the soil only change temporarily with the growing periods, but is hardly affected by the planting of the transgenic cotton.
Keywords:arbuscular mycorrhizal fungi  transgenic cotton  Polymerase chain reaction-Denaturing gradient gel electrophoresis (PCR-DGGE)
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