Microbial carbon use efficiency and priming effect regulate soil carbon storage under nitrogen deposition by slowing soil organic matter decomposition

[1]  P. Ciais,et al.  Changes in nutrient concentrations of leaves and roots in response to global change factors , 2017, Global change biology.

[2]  B. Hungate,et al.  Bacterial carbon use plasticity, phylogenetic diversity and the priming of soil organic matter , 2017, The ISME Journal.

[3]  I. Kögel‐Knabner,et al.  Anthropogenic N deposition increases soil organic matter accumulation without altering its biochemical composition , 2017, Global change biology.

[4]  G. Ågren,et al.  Combining theory and experiment to understand effects of inorganic nitrogen on litter decomposition , 2001, Oecologia.

[5]  S. Hobbie,et al.  Mechanisms driving the soil organic matter decomposition response to nitrogen enrichment in grassland soils , 2016 .

[6]  Wei Zhang,et al.  High nitrogen deposition decreases the contribution of fungal residues to soil carbon pools in a tropical forest ecosystem , 2016 .

[7]  W. Wanek,et al.  Soil microbial carbon use efficiency and biomass turnover in a long-term fertilization experiment in a temperate grassland. , 2016 .

[8]  K. Denef,et al.  Long-term reactive nitrogen loading alters soil carbon and microbial community properties in a subalpine forest ecosystem , 2016 .

[9]  R. Dalal,et al.  Effect of added nitrogen on plant litter decomposition depends on initial soil carbon and nitrogen stoichiometry , 2015 .

[10]  Noah Fierer,et al.  Consistent responses of soil microbial communities to elevated nutrient inputs in grasslands across the globe , 2015, Proceedings of the National Academy of Sciences.

[11]  Clare E. Kazanski,et al.  Nitrogen addition changes grassland soil organic matter decomposition , 2015, Biogeochemistry.

[12]  C. Jin,et al.  The effects of simulated nitrogen deposition on plant root traits: A meta-analysis , 2015 .

[13]  Jizhong Zhou,et al.  Methods for estimating temperature sensitivity of soil organic matter based on incubation data: A comparative evaluation , 2015 .

[14]  W. Shen,et al.  High clay content accelerates the decomposition of fresh organic matter in artificial soils , 2014 .

[15]  W. McDowell,et al.  Chronic nitrogen additions suppress decomposition and sequester soil carbon in temperate forests , 2014, Biogeochemistry.

[16]  S. Blagodatsky,et al.  Soil C and N availability determine the priming effect: microbial N mining and stoichiometric decomposition theories , 2014, Global change biology.

[17]  Lin Jiang,et al.  Decoupling of soil microbes and plants with increasing anthropogenic nitrogen inputs in a temperate steppe , 2014 .

[18]  F. Hagedorn,et al.  Nitrogen deposition promotes the production of new fungal residues but retards the decomposition of old residues in forest soil fractions , 2014, Global change biology.

[19]  Y. Carrillo,et al.  Rhizosphere priming: a nutrient perspective , 2013, Front. Microbiol..

[20]  Stefano Manzoni,et al.  Carbon use efficiency of microbial communities: stoichiometry, methodology and modelling. , 2013, Ecology letters.

[21]  K. Denef,et al.  The Microbial Efficiency‐Matrix Stabilization (MEMS) framework integrates plant litter decomposition with soil organic matter stabilization: do labile plant inputs form stable soil organic matter? , 2013, Global change biology.

[22]  J. Six,et al.  The temperature response of soil microbial efficiency and its feedback to climate , 2013 .

[23]  M. Reichstein,et al.  Both priming and temperature sensitivity of soil organic matter decomposition depend on microbial biomass--An incubation study , 2013 .

[24]  Andreas Richter,et al.  Environmental and stoichiometric controls on microbial carbon-use efficiency in soils. , 2012, The New phytologist.

[25]  D. Tilman,et al.  Soil carbon sequestration in prairie grasslands increased by chronic nitrogen addition. , 2012, Ecology.

[26]  Petr Baldrian,et al.  Cellulose utilization in forest litter and soil: identification of bacterial and fungal decomposers. , 2012, FEMS microbiology ecology.

[27]  Rob Knight,et al.  Comparative metagenomic, phylogenetic and physiological analyses of soil microbial communities across nitrogen gradients , 2011, The ISME Journal.

[28]  E. Bååth,et al.  Use and misuse of PLFA measurements in soils , 2011 .

[29]  P. Brookes,et al.  Fungal and bacterial growth responses to N fertilization and pH in the 150-year 'Park Grass' UK grassland experiment. , 2011, FEMS microbiology ecology.

[30]  I. Jamieson,et al.  Multimodel inference in ecology and evolution: challenges and solutions , 2011, Journal of evolutionary biology.

[31]  T. L. Dickson,et al.  Fertilization decreases plant biodiversity even when light is not limiting. , 2011, Ecology letters.

[32]  B. Mary,et al.  Fungi mediate long term sequestration of carbon and nitrogen in soil through their priming effect , 2011 .

[33]  Y. Kuzyakov.  Priming effects : interactions between living and dead organic matter , 2010 .

[34]  W. Wanek,et al.  The effect of resource quantity and resource stoichiometry on microbial carbon-use-efficiency. , 2010, FEMS microbiology ecology.

[35]  Lingli Liu,et al.  A global perspective on belowground carbon dynamics under nitrogen enrichment. , 2010, Ecology letters.

[36]  Jianguo Wu,et al.  Tradeoffs and thresholds in the effects of nitrogen addition on biodiversity and ecosystem functioning: evidence from inner Mongolia Grasslands , 2010 .

[37]  P. Reich,et al.  Interactive Effects of Time, CO2, N, and Diversity on Total Belowground Carbon Allocation and Ecosystem Carbon Storage in a Grassland Community , 2009, Ecosystems.

[38]  W. Bowman,et al.  Negative impact of nitrogen deposition on soil buffering capacity , 2008 .

[39]  K. Treseder.  Nitrogen additions and microbial biomass: a meta-analysis of ecosystem studies. , 2008, Ecology letters.

[40]  Fusuo Zhang,et al.  Evidence for organic N deposition and its anthropogenic sources in China , 2008 .

[41]  N. Fierer,et al.  Microbial nitrogen limitation increases decomposition. , 2007, Ecology.

[42]  G. Saiz,et al.  Assessment of soil CO2 efflux and its components using a process-based model in a young temperate forest site , 2007 .

[43]  D. Myrold,et al.  Microbial community utilization of added carbon substrates in response to long-term carbon input manipulation , 2006 .

[44]  J. Six,et al.  Do growth yield efficiencies differ between soil microbial communities differing in fungal : bacterial ratios? reality check and methodological issues , 2006 .

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

[46]  J. Six,et al.  Bacterial and Fungal Contributions to Carbon Sequestration in Agroecosystems , 2006 .

[47]  M. Firestone,et al.  Altered utilization patterns of young and old soil C by microorganisms caused by temperature shifts and N additions , 2004 .

[48]  E. Bååth,et al.  The use of phospholipid fatty acid analysis to estimate bacterial and fungal biomass in soil , 1996, Biology and Fertility of Soils.

[49]  Joshua P. Schimel,et al.  The implications of exoenzyme activity on microbial carbon and nitrogen limitation in soil: a theoretical model , 2003 .

[50]  J. L. Smith,et al.  Priming effect and C storage in semi-arid no-till spring crop rotations , 2003, Biology and Fertility of Soils.

[51]  K. Paustian,et al.  Influence of microbial populations and residue quality on aggregate stability , 2001 .

[52]  W. Horwath,et al.  Decomposition of rice straw and microbial carbon use efficiency under different soil temperatures and moistures , 2000 .