【摘 要】
：
Soil samples were collected from three plots under different land utilization patterns including degradation,farming,and restoration.The abundances of methanotr
【机 构】
：
State Key Laboratory of Urban and Regional Ecology,Key Laboratory of Systematic Mycology and Licheno
【基金项目】
：
the Knowledge Innovation Program of Chinese Academy of Sciences;the Natural Science Foundation of China
论文部分内容阅读
Soil samples were collected from three plots under different land utilization patterns including degradation,farming,and restoration.The abundances of methanotrophs were quantified using real-time polymerase chain reaction(PCR)based on the pmoA and 16S rRNA genes,and the community fingerprint was analyzed using denaturing gradient gel electrophoresis(DGGE)aiming at pmoA gene.Significantly lower 16S rRNA and pmoA genes copies were found in the degradation treatment than in farming and restoration.Higher abundances of Type Ⅰ than those of Type Ⅱ methanotrophs were detected in all treatments.The treatment of farming was clearly separated from degradation and restoration according to the DGGE profile by cluster analysis.The lowest diversity indices were observed in the F(farming plot),suggesting that the community structure was strongly affected by farming activities.There were significantly positive correlations between the copy numbers of pmoA also Type Ⅱ-related 16S rRNA genes and soil available K content.Strong negative and positive correlations were found between Type Ⅰ and soil pH,and available P content,respectively.We concluded that the vegetation cover or not,soil characteristics including pH and nutrients of P and K as a result of anthropogenic disturbance may be key factors affecting methanotrophic communities in upland soil.
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