Elevational patterns of microbial carbon use efficiency in a subtropical mountain forest

[1]  K. Mganga,et al.  Microbial carbon use efficiency along an altitudinal gradient , 2022, Soil Biology and Biochemistry.

[2]  Yingjun Zhang,et al.  Repeated litter inputs promoted stable soil organic carbon formation by increasing fungal dominance and carbon use efficiency , 2022, Biology and Fertility of Soils.

[3]  P. He,et al.  Effect of different decay classes of Eucalyptus stump substrates on microbial resource limitation and carbon-use efficiency , 2022, Plant and Soil.

[4]  D. Moorhead,et al.  Estimating microbial carbon use efficiency in soil: Isotope-based and enzyme-based methods measure fundamentally different aspects of microbial resource use , 2022, Soil Biology and Biochemistry.

[5]  Jian Deng,et al.  Resource limitation and modeled microbial metabolism along an elevation gradient , 2022, CATENA.

[6]  Qianggong Zhang,et al.  Soil microbial trait-based strategies drive metabolic efficiency along an altitude gradient , 2021, ISME Communications.

[7]  C. Liang,et al.  Microbial necromass as the source of soil organic carbon in global ecosystems , 2021, Soil Biology and Biochemistry.

[8]  Lei Wu,et al.  Long-term manuring increases microbial carbon use efficiency and mitigates priming effect via alleviated soil acidification and resource limitation , 2021, Biology and Fertility of Soils.

[9]  Wei Wang,et al.  The effect of soil depth on temperature sensitivity of extracellular enzyme activity decreased with elevation: Evidence from mountain grassland belts. , 2021, The Science of the total environment.

[10]  F. Dijkstra,et al.  Microbial carbon use efficiency, biomass residence time and temperature sensitivity across ecosystems and soil depths , 2021 .

[11]  Dongwei Liu,et al.  Large‐scale importance of microbial carbon use efficiency and necromass to soil organic carbon , 2021, Global change biology.

[12]  Huimin Wang,et al.  Litter manipulation effects on microbial communities and enzymatic activities vary with soil depth in a subtropical Chinese fir plantation , 2021 .

[13]  Y. Liao,et al.  Microbial carbon-use efficiency and straw-induced priming effect within soil aggregates are regulated by tillage history and balanced nutrient supply , 2021, Biology and Fertility of Soils.

[14]  Xinhui Han,et al.  Adaptive pathways of soil microorganisms to stoichiometric imbalances regulate microbial respiration following afforestation in the Loess Plateau, China , 2020 .

[15]  K. DeAngelis,et al.  Heavy and wet: The consequences of violating assumptions of measuring soil microbial growth efficiency using the 18O water method , 2020, Elementa: Science of the Anthropocene.

[16]  E. Bai,et al.  Evaluation of the 18O-H2O incubation method for measurement of soil microbial carbon use efficiency , 2020 .

[17]  Yichao Rui,et al.  Microbial carbon use efficiency, biomass turnover, and necromass accumulation in paddy soil depending on fertilization , 2020 .

[18]  W. Wanek,et al.  Quantifying microbial growth and carbon use efficiency in dry soil environments via 18O water vapor equilibration , 2020, Global change biology.

[19]  S. Frey,et al.  Microbial diversity drives carbon use efficiency in a model soil , 2020, Nature Communications.

[20]  Huan-shi Zhang,et al.  The nutrient release rate accounts for the effect of organic matter type on soil microbial carbon use efficiency of a Pinus tabulaeformis forest in northern China , 2019, Journal of Soils and Sediments.

[21]  M. Bradford,et al.  Increasing microbial carbon use efficiency with warming predicts soil heterotrophic respiration globally , 2019, Global change biology.

[22]  F. Dijkstra,et al.  Carbon and phosphorus addition effects on microbial carbon use efficiency, soil organic matter priming, gross nitrogen mineralization and nitrous oxide emission from soil , 2019, Soil Biology and Biochemistry.

[23]  G. Pan,et al.  Organic carbon quality, composition of main microbial groups, enzyme activities, and temperature sensitivity of soil respiration of an acid paddy soil treated with biochar , 2019, Biology and Fertility of Soils.

[24]  W. Wanek,et al.  Growth explains microbial carbon use efficiency across soils differing in land use and geology , 2018, Soil biology & biochemistry.

[25]  L. Schipper,et al.  The optimum temperature of soil microbial respiration: Patterns and controls , 2018, Soil Biology and Biochemistry.

[26]  Zehao Shen,et al.  Stair-Step Pattern of Soil Bacterial Diversity Mainly Driven by pH and Vegetation Types Along the Elevational Gradients of Gongga Mountain, China , 2018, Front. Microbiol..

[27]  L. Kruuk,et al.  Microbes follow Humboldt: temperature drives plant and soil microbial diversity patterns from the Amazon to the Andes , 2018, Ecology.

[28]  Guirui Yu,et al.  Changes in nitrogen-cycling microbial communities with depth in temperate and subtropical forest soils , 2017 .

[29]  T. Cajthaml,et al.  Altitudinal, seasonal and interannual shifts in microbial communities and chemical composition of soil organic matter in Alpine forest soils , 2017 .

[30]  J. Jastrow,et al.  The importance of anabolism in microbial control over soil carbon storage , 2017, Nature Microbiology.

[31]  G. Guggenberger,et al.  Microbial Community Dynamics in Soil Depth Profiles Over 120,000 Years of Ecosystem Development , 2017, Front. Microbiol..

[32]  S. Frey,et al.  Direct evidence for microbial-derived soil organic matter formation and its ecophysiological controls , 2016, Nature Communications.

[33]  J. Beman,et al.  Microbial diversity and community structure along a lake elevation gradient in Yosemite National Park, California, USA. , 2016, Environmental microbiology.

[34]  D. Moorhead,et al.  Stoichiometry of microbial carbon use efficiency in soils , 2016 .

[35]  W. Wanek,et al.  Microbial carbon use efficiency and biomass turnover times depending on soil depth – Implications for carbon cycling , 2016 .

[36]  Benjamin L Turner,et al.  Soil microbial nutrient constraints along a tropical forest elevation gradient: a belowground test of a biogeochemical paradigm , 2015 .

[37]  Paul Dijkstra,et al.  Accelerated microbial turnover but constant growth efficiency with warming in soil , 2014 .

[38]  P. Christie,et al.  Soil microbial community structure and activity along a montane elevational gradient on the Tibetan Plateau , 2014 .

[39]  D. Bates,et al.  Fitting Linear Mixed-Effects Models Using lme4 , 2014, 1406.5823.

[40]  W. Wanek,et al.  Stoichiometric imbalances between terrestrial decomposer communities and their resources: mechanisms and implications of microbial adaptations to their resources , 2014, Front. Microbiol..

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

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

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

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

[45]  Ji‐Zheng He,et al.  Distribution and diversity of archaeal communities in selected Chinese soils. , 2012, FEMS microbiology ecology.

[46]  P. Brookes,et al.  Measuring soil microbial biomass using an automated procedure , 2011 .

[47]  Zhiqun Huang,et al.  Long-term nitrogen additions increased surface soil carbon concentration in a forest plantation despite elevated decomposition , 2011 .

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

[49]  Mark A. Bradford,et al.  Soil-carbon response to warming dependent on microbial physiology , 2010 .

[50]  P. Brookes,et al.  Substrate inputs and pH as factors controlling microbial biomass, activity and community structure in an arable soil , 2009 .

[51]  R. B. Jackson,et al.  Toward an ecological classification of soil bacteria. , 2007, Ecology.

[52]  R. Conrad,et al.  High abundance of Crenarchaeota in a temperate acidic forest soil. , 2007, FEMS microbiology ecology.

[53]  M. Niklińska,et al.  Effect of temperature on the respiration rate of forest soil organic layer along an elevation gradient in the Polish Carpathians , 2007, Biology and Fertility of Soils.

[54]  Changming Zhao,et al.  Altitudinal Pattern of Plant Species Diversity in Shennongjia Mountains, Central China , 2005 .

[55]  J. Whalen,et al.  A microplate assay to measure soil microbial biomass phosphorus , 2004, Biology and Fertility of Soils.

[56]  R. Bartha,et al.  Metabolic efficiency and turnover of soil microbial communities in biodegradation tests , 1996, Applied and environmental microbiology.

[57]  J. G. Kuenen,et al.  Biochemical limits to microbial growth yields: An analysis of mixed substrate utilization , 1988, Biotechnology and bioengineering.

[58]  S. Frey,et al.  Clarifying the interpretation of carbon use efficiency in soil through methods comparison , 2019, Soil Biology and Biochemistry.

[59]  I. Kögel‐Knabner,et al.  Deep soil organic matter—a key but poorly understood component of terrestrial C cycle , 2010, Plant and Soil.