Methanogenic Pathway and Archaeal Communities in Three Different Anoxic Soils Amended with Rice Straw and Maize Straw

Addition of straw is common practice in rice agriculture, but its effect on the path of microbial CH4 production and the microbial community involved is not well known. Since straw from rice (C3 plant) and maize plants (C4 plant) exhibit different δ13C values, we compared the effect of these straw types using anoxic rice field soils from Italy and China, and also a soil from Thailand that had previously not been flooded. The temporal patterns of production of CH4 and its major substrates H2 and acetate, were slightly different between rice straw and maize straw. Addition of methyl fluoride, an inhibitor of acetoclastic methanogenesis, resulted in partial inhibition of acetate consumption and CH4 production. The δ13C of the accumulated CH4 and acetate reflected the different δ13C values of rice straw versus maize straw. However, the relative contribution of hydrogenotrophic methanogenesis to total CH4 production exhibited a similar temporal change when scaled to CH4 production irrespectively of whether rice straw or maize straw was applied. The composition of the methanogenic archaeal communities was characterized by terminal restriction fragment length polymorphism (T-RFLP) analysis and was quantified by quantitative PCR targeting archaeal 16S rRNA genes or methanogenic mcrA genes. The size of the methanogenic communities generally increased during incubation with straw, but the straw type had little effect. Instead, differences were found between the soils, with Methanosarcinaceae and Methanobacteriales dominating straw decomposition in Italian soil, Methanosarcinaceae, Methanocellales, and Methanobacteriale in China soil, and Methanosarcinaceae and Methanocellales in Thailand soil. The experiments showed that methanogenic degradation in different soils involved different methanogenic population dynamics. However, the path of CH4 production was hardly different between degradation of rice straw versus maize straw and was also similar for the different soil types.

[1]  P. Claus,et al.  Methanogenic archaea are globally ubiquitous in aerated soils and become active under wet anoxic conditions , 2011, The ISME Journal.

[2]  R. Conrad,et al.  Responses of Methanogen mcrA Genes and Their Transcripts to an Alternate Dry/Wet Cycle of Paddy Field Soil , 2011, Applied and Environmental Microbiology.

[3]  R. Conrad,et al.  Activation of Methanogenesis in Arid Biological Soil Crusts Despite the Presence of Oxygen , 2011, PloS one.

[4]  A. Mishra,et al.  In vitro methane emission from Indian dry roughages in relation to chemical composition , 2011 .

[5]  Y. Kuzyakov,et al.  13C fractionation at the root-microorganisms-soil interface: A review and outlook for partitioning studies , 2010 .

[6]  D. Hannaway,et al.  Comparison of crop simulation and field performance of maize under 20-day dry period imposed during selected critical growth periods in Nakhon Ratchasima Province, Thailand. , 2010 .

[7]  K. Majumdar,et al.  Rice-maize systems of South Asia: current status, future prospects and research priorities for nutrient management , 2010, Plant and Soil.

[8]  Ke Ma,et al.  Microbial mechanism for rice variety control on methane emission from rice field soil , 2009 .

[9]  P. Claus,et al.  Activity and composition of the methanogenic archaeal community in soil vegetated with wild versus cultivated rice , 2009 .

[10]  Ke Ma,et al.  Composition of Archaeal Community in a Paddy Field as Affected by Rice Cultivar and N Fertilizer , 2009, Microbial Ecology.

[11]  R. Conrad,et al.  Effect of Substrate Concentration on Carbon Isotope Fractionation during Acetoclastic Methanogenesis by Methanosarcina barkeri and M. acetivorans and in Rice Field Soil , 2009, Applied and Environmental Microbiology.

[12]  K. Yagi,et al.  Methane emission from paddy soils as affected by wheat straw returning mode , 2008, Plant and Soil.

[13]  Yahai Lu,et al.  Dynamics of the Methanogenic Archaeal Community during Plant Residue Decomposition in an Anoxic Rice Field Soil , 2008, Applied and Environmental Microbiology.

[14]  R. Conrad,et al.  Soil type links microbial colonization of rice roots to methane emission , 2008 .

[15]  R. Bol,et al.  Combining biomarker with stable isotope analyses for assessing the transformation and turnover of soil organic matter , 2008 .

[16]  R. Conrad,et al.  Quantification of carbon flow from stable isotope fractionation in rice field soils with different organic matter content , 2007 .

[17]  P. Claus,et al.  Characterization of methanogenic Archaea and stable isotope fractionation during methane production in the profundal sediment of an oligotrophic lake (Lake Stechlin, Germany) , 2007 .

[18]  R. Conrad Microbial Ecology of Methanogens and Methanotrophs , 2007 .

[19]  R. Conrad,et al.  Dynamics of the methanogenic archaeal community in anoxic rice soil upon addition of straw , 2006 .

[20]  P. Claus,et al.  Carbon Isotope Fractionation during Acetoclastic Methanogenesis by Methanosaeta concilii in Culture and a Lake Sediment , 2006, Applied and Environmental Microbiology.

[21]  Werner Liesack,et al.  Genome of Rice Cluster I Archaea—the Key Methane Producers in the Rice Rhizosphere , 2006, Science.

[22]  S. Tyler,et al.  Determination of isotope fractionation factors and quantification of carbon flow by stable carbon isotope signatures in a methanogenic rice root model system , 2006 .

[23]  Yakov Kuzyakov,et al.  Sources of CO2 efflux from soil and review of partitioning methods , 2006 .

[24]  R. Conrad,et al.  Effect of Inhibition of Acetoclastic Methanogenesis on Growth of Archaeal Populations in an Anoxic Model Environment , 2006, Applied and Environmental Microbiology.

[25]  W. Seiler,et al.  Effects of vegetation on the emission of methane from submerged paddy soil , 1986, Plant and Soil.

[26]  R. Conrad,et al.  Abundance and activity of uncultured methanotrophic bacteria involved in the consumption of atmospheric methane in two forest soils. , 2005, Environmental microbiology.

[27]  K. Yagi,et al.  Statistical analysis of the major variables controlling methane emission from rice fields , 2005 .

[28]  R. Conrad Quantification of methanogenic pathways using stable carbon isotopic signatures: a review and a proposal , 2005 .

[29]  Jaai Kim,et al.  Group-specific primer and probe sets to detect methanogenic communities using quantitative real-time polymerase chain reaction. , 2005, Biotechnology and bioengineering.

[30]  R. Conrad,et al.  Activity, structure and dynamics of the methanogenic archaeal community in a flooded Italian rice field. , 2005, FEMS microbiology ecology.

[31]  A. Chidthaisong,et al.  Carbon and hydrogen isotope fractionation by moderately thermophilic methanogens , 2004 .

[32]  P. Claus,et al.  Temporal change of 13C-isotope signatures and methanogenic pathways in rice field soil incubated anoxically at different temperatures , 2004 .

[33]  R. Conrad Control of microbial methane production in wetland rice fields , 2002, Nutrient Cycling in Agroecosystems.

[34]  M. Kimura,et al.  Estimation of the increase in CH4 emission from paddy soils by rice straw application , 1995, Plant and Soil.

[35]  P. Claus,et al.  Pathway of CH4 formation in anoxic rice field soil and rice roots determined by 13C-stable isotope fractionation. , 2002, Chemosphere.

[36]  A. Chidthaisong,et al.  A comparison of isotope fractionation of carbon and hydrogen from paddy field rice roots and soil bacterial enrichments during CO , 2002 .

[37]  R. Conrad,et al.  Seasonal variation in pathways of CH4 production and in CH4 oxidation in rice fields determined by stable carbon isotopes and specific inhibitors , 2002 .

[38]  R. Conrad,et al.  Saccharolytic activity and its role as a limiting step in methane formation during the anaerobic degradation of rice straw in rice paddy soil , 2002, Biology and Fertility of Soils.

[39]  R. Conrad,et al.  Methanogenic populations involved in the degradation of rice straw in anoxic paddy soil , 2001 .

[40]  Weixin Cheng,et al.  Photosynthesis controls of rhizosphere respiration and organic matter decomposition , 2001 .

[41]  Hua Xu,et al.  CH4 emissions from rice paddies managed according to farmer's practice in Hunan, China , 2001 .

[42]  Charles T. Garten,et al.  Separating root and soil microbial contributions to soil respiration: A review of methods and observations , 2000 .

[43]  T. Lueders,et al.  Archaeal Population Dynamics during Sequential Reduction Processes in Rice Field Soil , 2000, Applied and Environmental Microbiology.

[44]  W. Merbach,et al.  The Origin of Soil Organic C, Dissolved Organic C and Respiration in a Long‐Term Maize Experiment in Halle, Germany, Determined by 13C Natural Abundance , 2000 .

[45]  S. Tyler,et al.  Differences in CH4 oxidation and pathways of production between rice cultivars deduced from measurements of CH4 flux and δ13C of CH4 and CO2 , 1999 .

[46]  M. Kimura,et al.  Evaluation of origins of CH4 carbon emitted from rice paddies , 1999 .

[47]  Klose,et al.  Anaerobic conversion of carbon dioxide to methane, acetate and propionate on washed rice roots. , 1999, FEMS microbiology ecology.

[48]  R. Conrad,et al.  How specific is the inhibition by methyl fluoride of acetoclastic methanogenesis in anoxic rice field soil , 1999 .

[49]  P. Rochette,et al.  Separating Soil Respiration into Plant and Soil Components Using Analyses of the Natural Abundance of Carbon‐13 , 1999 .

[50]  R. Conrad,et al.  Effect of Temperature on Structure and Function of the Methanogenic Archaeal Community in an Anoxic Rice Field Soil , 1999, Applied and Environmental Microbiology.

[51]  R. Conrad Contribution of hydrogen to methane production and control of hydrogen concentrations in methanogenic soils and sediments , 1999 .

[52]  M. Kimura,et al.  Contribution of rice straw carbon to CH4 emission from rice paddies using 13C‐enriched rice straw , 1998 .

[53]  W. Liesack,et al.  Diversity and Structure of the Methanogenic Community in Anoxic Rice Paddy Soil Microcosms as Examined by Cultivation and Direct 16S rRNA Gene Sequence Retrieval , 1998, Applied and Environmental Microbiology.

[54]  P. Janssen,et al.  Inhibition of methanogenesis by methyl fluoride: studies of pure and defined mixed cultures of anaerobic bacteria and archaea , 1997, Applied and environmental microbiology.

[55]  A. Chidthaisong,et al.  Methane formation and emission from flooded rice soil incorporated with 13C-labeled rice straw , 1997 .

[56]  R. Conrad,et al.  Sequential reduction processes and initiation of CH4 production upon flooding of oxic upland soils , 1996 .

[57]  H. Neue,et al.  Influence of organic matter incorporation on the methane emission from a wetland rice field , 1995 .

[58]  M. Kimura,et al.  Contribution of photosynthesized carbon to the methane emitted from paddy fields , 1994 .

[59]  A. Sugimoto,et al.  Carbon isotopic composition of bacterial methane in a soil incubation experiment: Contributions of acetate and CO2H2 , 1993 .

[60]  J. Hayes Factors controlling 13C contents of sedimentary organic compounds: Principles and evidence , 1993 .

[61]  L. Brussaard,et al.  Biological effects of plant residues with contrasting chemical compositions under humid tropical conditions-decomposition and nutrient release , 1992 .

[62]  J. Balesdent,et al.  Maize root-derived soil organic carbon estimated by natural 15c abundance , 1992 .

[63]  R. Conrad,et al.  Metabolism of position-labelled glucose in anoxic methanogenic paddy soil and lake sediment , 1991 .

[64]  R. Conrad,et al.  Factors influencing the population of methanogenic bacteria and the initiation of methane production upon flooding of paddy soil , 1990 .

[65]  Helmut Schütz,et al.  A 3-year continuous record on the influence of daytime, season, and fertilizer treatment on methane emission rates from an Italian rice paddy , 1989 .

[66]  J. Ehleringer,et al.  Carbon Isotope Discrimination and Photosynthesis , 1989 .