2006
DOI: 10.1016/j.soilbio.2005.09.020
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Community structure of methanogenic archaea in paddy field soil under double cropping (rice–wheat)

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Cited by 120 publications
(123 citation statements)
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“…6). This stability of methanogen populations has also been observed previously (19,27,46). In the drainage treatment, however, the growth of methanogenic populations, as revealed by mcrA gene abundance, was suppressed in four soil compartments during the second dry/wet cycle.…”
Section: Discussionsupporting
confidence: 85%
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“…6). This stability of methanogen populations has also been observed previously (19,27,46). In the drainage treatment, however, the growth of methanogenic populations, as revealed by mcrA gene abundance, was suppressed in four soil compartments during the second dry/wet cycle.…”
Section: Discussionsupporting
confidence: 85%
“…In addition, O 2 stress could also repress the mcrA transcription, although it recovered to some extent after reflooding (52). Alternate dry/wet cycles did not influence the structure of the methanogenic community, a finding consistent with several earlier studies demonstrating the stable structure of methanogenic archaea in rice field soil under different conditions (17,27,46,51). A recent study using the traditional culture method also showed no effects of water management on the methanogenic community (14).…”
Section: Discussionsupporting
confidence: 84%
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“…The spike addition of additional acetate (Fig 5B, day 15 Although methanogens have been found in various environments such as human dental plaque (Kulik et al, 2001), and rice paddy (Watanabe et al, 2006), the current study shows the first evidence of the systematic presence of thermophilic methanogens in grass lawn. To explain this finding, further study is required addressing questions such as below:…”
Section: Comparison Of Methane Production Of Turf Grass Samples From mentioning
confidence: 58%
“…Real-time PCR was carried out to quantify the methanogenic archaea 16S rRNA genes in soil samples using LightCycler ST300, LightCycler Software Version 3.5 (Roche Diagnostics, Germany) and SYBR Premix Ex Taq (TaKaRa, Japan). The primer pair 1106F (forward) and 1378R (reverse) was used for PCR amplification targeting the 16S rRNA gene of methanogenic archaea (Watanabe et al, 2006(Watanabe et al, , 2009. Each reaction mixture (25 µl) consisted of 12.5 µl 1×SYBR Premix Ex Taq, 0.25 µl of each primer, 1 µl of DNA template diluted 20 times, and sterilize distilled water.…”
Section: Dna Extraction and Real-time Pcrmentioning
confidence: 99%