用户名: 密码: 验证码:
Dynamics of bacterial communities in relation to soil aggregate formation during the decomposition of 13C-labelled rice straw
详细信息查看全文 | 推荐本文 |
摘要
The addition of fresh organic matter is known to modify both microbial community structure and soil aggregation. The objective of this study was to understand the relationship between the dynamics of the soil microbial community structure in relation to that of their habitats during the decomposition of straw. Soil samples, ground (<200 渭m) to remove macroaggregates, were amended with uniformly 13C-labelled powdered rice straw (<500 渭m) and incubated for 21 days. Unamended control samples were also incubated under the same conditions. Total C and rice straw C (CStraw) mineralised or remaining in different soil fractions (0-50, 50-200, 200-2000 and >2000 渭m) were measured. Fatty acid methyl ester (FAME) profiling was used to determine total bacterial community structure and FAME based stable isotope probing (FAME-SIP) was used to characterise the straw degrader communities. The mineralisation rate of the native C and the CStraw was high. The formation of macroaggregates (>2000 渭m) occurred within 2 days in amended and unamended samples but did so to a greater extent in the amended samples. The CStraw was mainly located in fractions >200 渭m, where degraders were the most abundant. The 13C-FAME profiles followed the same trends as total FAME profiles through time and within soil fractions, suggesting common dynamics between straw degraders and total bacterial communities: Gram-negative were more important in fraction >200 渭m and during the early stages of the incubation while Gram-positive and actinobacteria dominated in fine fractions and at the end of the incubation. Bacterial community structure changed rapidly (within 2 days) in conjunction with the formation of new microbial habitats, suggesting that the relationship between the two is very close.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700