Impact of fumigants on soil microbial communities

被引:206
作者
Ibekwe, AM
Papiernik, SK
Gan, J
Yates, SR
Yang, CH
Crowley, DE
机构
[1] USDA ARS, George E Brown Jr Salin Lab, Riverside, CA 92507 USA
[2] Univ Calif Riverside, Dept Environm Sci, Riverside, CA 92521 USA
关键词
D O I
10.1128/AEM.67.7.3245-3257.2001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Agricultural soils are typically fumigated to provide effective control of nematodes, soilborne pathogens, and weeds in preparation for planting of high-value cash crops. The ability of soil microbial communities to recover after treatment with fumigants was examined using culture-dependent (Biolog) and culture-independent (phospholipid fatty acid [PLFA] analysis and denaturing gradient gel electrophoresis [DGGE] of 16S ribosomal DNA [rDNA] fragments amplified directly from soil DNA) approaches. Changes in soil microbial community structure were examined in a microcosm experiment following the application of methyl bromide (MeBr), methyl isothiocyanate, 1,3-dichloropropene (1,3-D), and chloropicrin, Variations among Biolog fingerprints showed that the effect of MeBr on heterotrophic microbial activities was most severe in the first week and that thereafter the effects of MeBr and the other fumigants were expressed at much lower levels. The results of PLFA analysis demonstrated a community shift in all treatments to a community dominated by gram-positive bacterial biomass, Different 16S rDNA profiles from fumigated soils were quantified by analyzing the DGGE band patterns. The Shannon-Weaver index of diversity, H, was calculated for each fumigated soil sample. High diversity indices were maintained between the control soil and the fumigant-treated soils, except for MeBr (H decreased from 1.14 to 0.13), After 12 weeks of incubation, H increased to 0.73 in the MeBr-treated samples. Sequence analysis of clones generated from unique bands showed the presence of taxonomically unique clones that had emerged from the MeBr-treated samples and were dominated by clones closely related to Bacillus spp, and Heliothrix oregonensis, Variations in the data were much higher in the Biolog assay than in the PLFA and DGGE assays, suggesting a high sensitivity of PLFA analysis and DGGE in monitoring the effects of fumigants on soil community composition and structure. Our results indicate that MeBr has the greatest impact on soil microbial communities and that 1,3-D has the least impact.
引用
收藏
页码:3245 / 3257
页数:13
相关论文
共 47 条
[31]  
Smalla K, 1998, APPL ENVIRON MICROB, V64, P1220
[32]   HIGH DIVERSITY IN DNA OF SOIL BACTERIA [J].
TORSVIK, V ;
GOKSOYR, J ;
DAAE, FL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1990, 56 (03) :782-787
[33]  
Vallaeys T, 1997, FEMS MICROBIOL ECOL, V24, P279, DOI 10.1111/j.1574-6941.1997.tb00445.x
[34]  
Weaver W., 1963, MATH THEORY COMMUNIC
[35]   In situ microbial ecology for quantitative appraisal, monitoring, and risk assessment of pollution remediation in soils, the subsurface, the rhizosphere and in biofilms [J].
White, DC ;
Flemming, CA ;
Leung, KT ;
Macnaughton, SJ .
JOURNAL OF MICROBIOLOGICAL METHODS, 1998, 32 (02) :93-105
[36]   BIOCHEMICAL MARKERS FOR MEASUREMENT OF PREDATION EFFECTS ON THE BIOMASS, COMMUNITY STRUCTURE, NUTRITIONAL-STATUS, AND METABOLIC-ACTIVITY OF MICROBIAL BIOFILMS [J].
WHITE, DC ;
FINDLAY, RH .
HYDROBIOLOGIA, 1988, 159 (01) :119-132
[37]   DETERMINATION OF THE SEDIMENTARY MICROBIAL BIOMASS BY EXTRACTABLE LIPID PHOSPHATE [J].
WHITE, DC ;
DAVIS, WM ;
NICKELS, JS ;
KING, JD ;
BOBBIE, RJ .
OECOLOGIA, 1979, 40 (01) :51-62
[38]  
Wintzingerode Friedrich V., 1997, FEMS Microbiology Reviews, V21, P213
[39]  
WUNSCHE L, 1995, FEMS MICROBIOL ECOL, V17, P295
[40]   Rhizosphere microbial community structure in relation to root location and plant iron nutritional status [J].
Yang, CH ;
Crowley, DE .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2000, 66 (01) :345-351