All Stories

  1. Fungal and bacterial necromass: Opposite drivers of mineral-associated organic carbon gains and losses
  2. Carbon pathways in soil: unraveled by 13C natural abundance
  3. Rhizosphere – detritusphere interactions stabilize soil carbon depending on plant litter traits
  4. Disentangling two and three domain laccases in soils: contribution of fungi, bacteria and abiotic processes to oxidative activities
  5. Faster soil organic carbon turnover in MAOM versus POM: straw input causes larger microbial driven soil organic carbon decomposition but higher straw accumulation in MAOM
  6. Belowground plant carbon and nitrogen exchange: plant-derived carbon inputs and pore structure formation
  7. Convergence and divergence of microbial communities in river- Qinghai lake sediment continuum on Tibetan Plateau
  8. High soil salinity reduces straw decomposition but primes soil organic carbon loss
  9. Aluminum and microplastic release from reflective agricultural films disrupt microbial communities and functions in soil
  10. Quantifying microbial necromass contributions to soil carbon sequestration under diverse cropland management practices: A meta-analysis
  11. Spatial dynamics of phosphorus mobilization by mycorrhiza
  12. Phosphorus enrichment mediates the responses of plant lignin and microbial necromass accumulation to nitrogen addition in subalpine forest soil
  13. Abiotic Nitrite Incorporation into Organic Matter in Volcanic and Non-Volcanic Soil Within Rainforest Ecosystems
  14. Cascading Effects Within Soil Food Web Amplify Fungal Biomass and Necromass Production
  15. Does restoration of degraded grasslands follow the theory of multiple stable states?
  16. Microbial strategies regulate organic carbon accumulation in saline paddy soils: A millennium chronosequence
  17. Drying-rewetting cycles decrease temperature sensitivity of soil organic matter decomposition
  18. In situ visualization of soil profile acidification and processes following nitrogen fertilization and liming
  19. Contrasting Exogenous and Endogenous Soil Microbial Carbon Use Efficiencies Under Global Changes
  20. Acidification of European croplands by nitrogen fertilization: Consequences for carbonate losses, and soil health
  21. Activation energy of soil organic matter decomposition
  22. Soil health: Critical evaluation and approaches
  23. Thirteen years of applying maize-derived organic materials and N fertilizers in North China Plain increased microbial CUE and NUE while increasing SOC and TN through necromass inputs.
  24. Modeling of CO2 Efflux from Forest and Grassland Soils Depending on Weather Conditions
  25. Humidity controls soil organic carbon accrual in grassland on the Qinghai–Tibet Plateau
  26. Management and rhizosphere microbial associations modulate genetic-driven nitrogen fate
  27. Mycorrhizal and nutrient controls of carbon sequestration in tropical rainforest soil
  28. Polylactic acid microplastics induced negative priming and improved carbon sequestration via microbial processes in different paddy soils
  29. Soil Health Under Global Change and Human Impact
  30. Contrasting effects of arsenic on mycorrhizal-mediated silicon and phosphorus uptake by rice
  31. Increased Mineral‐Associated Organic Carbon and Persistent Molecules in Allochthonous Blue Carbon Ecosystems
  32. Microbial Carbon Use Efficiency and Growth Rates in Soil: Global Patterns and Drivers
  33. Nitrogen availability in soil controls uptake of different nitrogen forms by plants
  34. Microbial rrn copy number is associated with soil C: N ratio and pH under long-term fertilization
  35. Multi-temporal assessment of a wildfire chronosequence by remote sensing
  36. Physicochemically protected organic carbon release is the rate-limiting step of rhizosphere priming in paddy soils
  37. Response of bacterial and fungal composition in tailings to Mn pollution
  38. Conventional agriculture increases global warming while decreasing system sustainability
  39. Effects of environmental changes on soil respiration in arid, cold, temperate, and tropical zones
  40. Energy storage and stability of soil organic matter during the natural restoration of abandoned cropland
  41. Fertilization shapes microbial life strategies, carbon and nitrogen metabolic functions in Camellia oleifera soil
  42. Ionic and nano calcium to reduce cadmium and arsenic toxicity in plants: Review of mechanisms and potentials
  43. Microbial composition in saline and alkaline soils regulates plant growth with P-solubilizing bacteria
  44. Root traits drive the recovery of soil nematodes during restoration of open mines in a tropical rainforest
  45. Conservation agriculture improves soil health and sustains crop yields after long-term warming
  46. Corrigendum to Razavi et al. (2016) “Rhizosphere shape of lentil and maize: Spatial distribution of enzyme activities” [Soil Biol. Biochem. 96, 229–237]
  47. Deciphering microbial drivers of soil organic matter mineralization in surface and subsurface soil during long-term vegetation succession
  48. Enzyme stoichiometry reveals microbial nitrogen limitation in stony soils
  49. Global research trends in Rhizodeposition-mediated soil carbon cycle: A bibliometric analysis
  50. Increased straw return promoted soil organic carbon accumulation in China's croplands over the past 40 years
  51. Influence of soil N availability on priming effects depending on temperature
  52. Inorganic Carbon Pools and Their Drivers in Grassland and Desert Soils
  53. Iron mineral type controls organic matter stability and priming in paddy soil under anaerobic conditions
  54. Organic matter composition and stability in estuarine wetlands depending on soil salinity
  55. Mycorrhizal growth and resource exchange define plant’s coexistence
  56. Assembly processes and co-occurrence of bacterial communities in tree rhizosphere under Pb-Zn contamination
  57. Drought effects on litter fraction and recovery in a subtropical forest
  58. Priming and balance of soil organic carbon differ with additive C:N ratios and long-term green manuring
  59. Soil nitrogen and phosphorus regulate decomposition of organic nitrogen compounds in the rothamsted experiment
  60. Biochar effects on crop yield variability
  61. General and specialized metabolites in peanut roots regulate arbuscular mycorrhizal symbiosis
  62. Linking nematode trophic diversity to plantation identity and soil nutrient cycling
  63. Long-term subsoiling and tillage rotation increase carbon storage in soil aggregates and the abundance of autotrophs
  64. Organic matter stability in forest-tundra soils after wildfire
  65. Limiting Resources Define the Global Pattern of Soil Microbial Carbon Use Efficiency
  66. Energy flows through nematode food webs depending on the soil carbon and nitrogen contents after forest conversion
  67. Microbial communities overwhelm environmental controls in explaining nitrous oxide emission in acidic soils
  68. Mechanisms of Arbuscular Mycorrhizal Fungi Increasing Silicon Uptake by Rice
  69. Effects of microbial groups on soil organic carbon accrual and mineralization during high- and low-quality litter decomposition
  70. Corrigendum to “Gross mineralization and nitrification in degraded alpine grassland soil” [Rhizosphere Volume 27, September 2023, 100778]
  71. Cyclic and linear trajectories of ecosystem evolution on sand dunes in Siberian taiga: A comprehensive analysis
  72. Extension of the soil monitoring network via tea bag initiatives: A 3000 km latitudinal gradient in European Russia
  73. Soil organic matter priming: The pH effects
  74. Rice rhizosphere microbiome is more diverse but less variable along environmental gradients compared to bulk soil
  75. Root mucilage nitrogen for rhizosphere microorganisms under drought
  76. Do Added Microplastics, Native Soil Properties, and Prevailing Climatic Conditions Have Consequences for Carbon and Nitrogen Contents in Soil? A Global Data Synthesis of Pot and Greenhouse Studies
  77. Invasive plant competitivity is mediated by nitrogen use strategies and rhizosphere microbiome
  78. Microbial response to long-term fertilization of paddy soils: Apparent and real priming effects
  79. Nitrification-induced acidity controls CO2 emission from soil carbonates
  80. Acidification of European croplands by nitrogen fertilization: Consequences for carbonate losses, and soil health
  81. Carbon footprint of maize-wheat cropping system after 40-year fertilization
  82. Microbial life‐history strategies mediate microbial carbon pump efficacy in response to N management depending on stoichiometry of microbial demand
  83. Composition and metabolism of microbial communities in soil pores
  84. Carbon starvation raises capacities in bacterial antibiotic resistance and viral auxiliary carbon metabolism in soils
  85. Bottom-up perspective – The role of roots and rhizosphere in climate change adaptation and mitigation in agroecosystems
  86. Alternate wetting-drying had no preferences for rice P uptake but increased microbial P allocation to phospholipids: Evidence from dual 32P and 33P labeling
  87. Carbon footprint of synthetic nitrogen under staple crops: A first cradle‐to‐grave analysis
  88. Decoupled response of microbial taxa and functions to nutrients: The role of stoichiometry in plantations
  89. Microbial phosphorus‐cycling genes in soil under global change
  90. Regulation of soil nitrogen cycling by shrubs in grasslands
  91. Rhizosphere engineering for soil carbon sequestration
  92. Soil organic carbon increase via microbial assimilation or soil protection against the priming effect is mediated by the availability of soil N relative to input C
  93. The wetter the better? Preferences in plant-microbial competition for phosphorus sources in rice cultivation under contrasting irrigation
  94. Corrigendum to “Habitat heterogeneity drives arbuscular mycorrhizal fungi and shrub communities in karst ecosystems” [CATENA 233 (2023) 107513]
  95. Soil organic carbon pools under long-term mineral and organic amendments: a multisite study
  96. Microbial diversity loss and wheat genotype-triggered rhizosphere bacterial and protistan diversity constrain soil multifunctionality: Evidence from greenhouse experiment
  97. Active microbial population dynamics and life strategies drive the enhanced carbon use efficiency in high-organic matter soils
  98. Deforestation impacts soil biodiversity and ecosystem services worldwide
  99. 3C natural abundance approach for analysis of steps of organic carbon transformation in soil: application for various ecosystems
  100. Arable Land Quality in Developing China: An Integrated Exploration from Global Challenges to Localized Solutions
  101. From energy to soil organic matter
  102. Inorganic carbon: an overlooked pool in global soil carbon research  
  103. Soil organic matter turnover: global implications from δ13C and δ15N signatures
  104. Soil zymography: a decade in microbial hotspot imaging and future challenges
  105. Grazing exclusion increases soil organic C through microbial necromass of root-derived C as traced by 13C labelling photosynthate
  106. Bacterial necromass determines the response of mineral-associated organic matter to elevated CO2
  107. Decreasing carbon allocation belowground in alpine meadow soils by shrubification
  108. Labile carbon inputs offset nitrogen-induced soil aggregate destabilization via enhanced growth of saprophytic fungi in a meadow steppe
  109. Microplastics alter soil structure and microbial community composition
  110. Inorganic carbon is overlooked in global soil carbon research: A bibliometric analysis
  111. Intensive N2 fixation accelerates microbial turnover in cropland soils
  112. Key role of microbial necromass and iron minerals in retaining micronutrients and facilitating biological nitrogen fixation in paddy soils
  113. Microbial mechanisms of organic matter mineralization induced by straw in biochar-amended paddy soil
  114. Microbial strategies for phosphorus acquisition in rice paddies under contrasting water regimes: Multiple source tracing by 32P and 33P
  115. Quantifying apparent and real priming effects based on inverse labelling
  116. Phosphorus (P) mobilisation from inorganic and organic P sources depends on P-acquisition strategies in dioecious Populus euphratica
  117. Nitrogen transformations in plastic-film mulched soils
  118. Multi-imaging platform for rhizosphere studies: Phosphorus and oxygen fluxes
  119. Straw addition and low soil moisture decreased temperature sensitivity and activation energy of soil organic matter
  120. “Energy and enthalpy” for microbial energetics in soil
  121. Soil organic matter turnover: Global implications from δ13C and δ15N signatures
  122. Microbially mediated mechanisms underlie soil carbon accrual by conservation agriculture under decade-long warming
  123. Arbuscular mycorrhizae mitigate negative impacts of soil biodiversity loss on grassland productivity
  124. Management and Rhizosphere Microbial Associations Modulate Genetic-Driven Nitrogen Fate
  125. Biochar Reduces N2o Emission from Fertilized Cropland Soils: A Meta-Analysis
  126. Crop Rotation Shapes the Fungal Rather than Bacterial Community for Enhanced Straw Degradation
  127. Drought Effects on Litter Composition and Recovery in a Subtropical Forest
  128. In Situ Visualisation of Soil Profile Acidification and Processes Following Nitrogen Fertilisation and Liming
  129. In Situ Visualization of Soil Profile Acidification and Processes Following Nitrogen Fertilization and Liming
  130. Mechanisms and implications of bacterial–fungal competition for soil resources
  131. Microbial interactions for nutrient acquisition in soil: Miners, scavengers, and carriers
  132. Mineralization and temperature sensitivity of soil organic matter pools of contrasting lability
  133. Nitrogen deposition raises temperature sensitivity of soil organic matter decomposition in subtropical forest
  134. Nitrogen fertilizer builds soil organic carbon under straw return mainly via microbial necromass formation
  135. Organic fertilizers incorporation increased microbial necromass accumulation more than mineral fertilization in paddy soil via altering microbial traits
  136. Earthworm Biopores for Transport and Nutrient Cycling
  137. Earthworms for Soil Organic Matter Mineralization and Carbon Sequestration
  138. Size matters: Aerobic methane oxidation in sediments of shallow thermokarst lakes
  139. Biochar and Microplastics Affect Microbial Necromass Accumulation and CO2 and N2O Emissions from Soil
  140. Microbial Necromass, Lignin, and Glycoproteins for Determining and Optimizing Blue Carbon Formation
  141. A stoichiometric approach to estimate sources of mineral‐associated soil organic matter
  142. Soil microbial richness and community composition are primarily mediated by functional trait diversity of fine roots in subtropical forests
  143. Contrasting impacts of plastic film mulching and nitrogen fertilization on soil organic matter turnover
  144. Contrasting mechanisms of nutrient mobilization in rhizosphere hotspots driven by straw and biochar amendment
  145. Key decomposers of straw depending on tillage and fertilization
  146. Local climate conditions explain the divergent climate change effects on (de)nitrification across the grassland biome: A meta-analysis
  147. Bacterial communities in cropland soils: Taxonomy and functions
  148. Labile substrate input weakens the memory effect of soil microbial functions under global warming
  149. Contrasting effects of maize straw and its biochar on aggregation and soil organic matter stabilization
  150. C:N:P stoichiometry of plants, soils, and microorganisms: Response to altered precipitation
  151. Fast labile carbon and litter exhaustion under no-tillage after 5-year soil warming
  152. Greenhouse gas emissions and mitigation in rice agriculture
  153. Drivers of microbially and plant‐derived carbon in topsoil and subsoil
  154. Accelerated organic matter decomposition in thermokarst lakes upon carbon and phosphorus inputs
  155. Bio-converted organic wastes shape microbiota in maize rhizosphere: Localization and identification in enzyme hotspots
  156. Effects of tillage on soil organic carbon and crop yield under straw return
  157. Shifts of understory vegetation induced by thinning drive the expansion of soil rare fungi
  158. Energy use efficiency of soil microorganisms: Driven by carbon recycling and reduction
  159. Organic carbon preservation in wetlands: Iron oxide protection vs. thermodynamic limitation
  160. Organic carbon accumulation and microbial activities in arable soils after abandonment: A chronosequence study
  161. Shower thoughts: why scientists should spend more time in the rain
  162. Dynamics of root–microbe interactions governing crop phosphorus acquisition after straw amendment
  163. Dual nature of soil structure: The unity of aggregates and pores
  164. Priming effect stimulates carbon release from thawed permafrost
  165. 3C natural abundance for analysis of steps of organic carbon transformation in soil: application for various ecosystems
  166. Microbial carbon use efficiency in soil under N deposition: Meta-analysis of 13C and 18O approaches
  167. Microbiome of rhizosphere: from structure and functions
  168. Soil inorganic carbon: stocks, functions, losses and their consequences
  169. Soil management effects on soil organic matter properties and carbon sequestration (SOMPACS)
  170. Soil organic matter as a mediator of energy fluxes - a new perspective
  171. Turnover of soil organic matter and microbial biomass under C3-C4 vegetation change: implications for carbon sequestration in Mediterranean agricultural soils.
  172. Carbon stabilization pathways in soil aggregates during long-term forest succession: Implications from δ13C signatures
  173. Microbial community succession in soil is mainly driven by carbon and nitrogen contents rather than phosphorus and sulphur contents
  174. Enzyme activities and organic matter mineralization in response to application of gypsum, manure and rice straw in saline and sodic soils
  175. Plant–soil–microbial interactions mediate vegetation succession in retreating glacial forefields
  176. Long-term phosphorus addition alleviates CO2 and N2O emissions via altering soil microbial functions in secondary rather primary tropical forests
  177. Soil warming decreases carbon availability and reduces metabolic functions of bacteria
  178. Time-dependent effects of microplastics on soil bacteriome
  179. Microbial necromass under global change and implications for soil organic matter
  180. Date palm cultivation: A review of soil and environmental conditions and future challenges
  181. Corrigendum to “Nitrite-dependent anaerobic oxidation decreases methane emissions from peatlands” [Soil Biology and Biochemistry 169, 108658]
  182. Effects of nitrogen and phosphorus fertilization on soil organic matter priming and net carbon balance in alpine meadows
  183. The role of rice cultivation in changes in atmospheric methane concentration and the Global Methane Pledge
  184. Functional traits of soil nematodes define their response to nitrogen fertilization
  185. Microbial necromass in cropland soils: A global meta‐analysis of management effects
  186. Large-scale ecosystem carbon stocks and their driving factors across Loess Plateau
  187. Long-term organic fertilizer-induced carbonate neoformation increases carbon sequestration in soil
  188. Linking bacterial life strategies with soil organic matter accrual by karst vegetation restoration
  189. Reductive dissolution of iron phosphate modifies rice root morphology in phosphorus-deficient paddy soils
  190. Elevated temperature and CO2 strongly affect the growth strategies of soil bacteria
  191. Mineral weathering is linked to microbial priming in the critical zone
  192. Fine root extension in urban forest soil depends on organic mulching
  193. Altered Organic Matter Chemical Functional Groups and Bacterial Community Composition Promote Crop Yield under Integrated Soil–Crop Management System
  194. Inducing Inorganic Carbon Accrual in Subsoil through Biochar Application on Calcareous Topsoil
  195. Long-term nitrogen and phosphorus fertilization reveals that phosphorus limitation shapes the microbial community composition and functions in tropical montane forest soil
  196. Bacterial Necromass Determines the Response of Mineral-Associated Organic Matter to Elevated Co2
  197. Straw Addition and Low Soil Moisture Decreased Temperature Sensitivity and Activation Energy of Soil Organic Matter
  198. Microplastics affect activity and spatial distribution of C, N, and P hydrolases in rice rhizosphere
  199. Frequent carbon input primes decomposition of decadal soil organic matter
  200. Generalists and specialists decomposing labile and aromatic biochar compounds and sequestering carbon in soil
  201. Dominant mycorrhizal association of trees determines soil nitrogen availability in subtropical forests
  202. Microbial utilization of photosynthesized carbon depends on land-use
  203. Soil quality and r – K fungal communities in plantations after conversion from subtropical forest
  204. Challenges in upscaling laboratory studies to ecosystems in soil microbiology research
  205. Experimental evidence for the impact of phages on mineralization of soil-derived dissolved organic matter under different temperature regimes
  206. Vegetation strategies for nitrogen and potassium acquisition along a climate and vegetation gradient: From semi-desert to temperate rainforest
  207. SARS-CoV-2 in Soil: A Microbial Perspective
  208. 5300‐Year‐old soil carbon is less primed than young soil organic matter
  209. Soil Chemical Properties Depending on Fertilization and Management in China: A Meta-Analysis
  210. Modelling the Rhizosphere Priming Effect in Combination with Soil Food Webs to Quantify Interaction between Living Plant, Soil Biota and Soil Organic Matter
  211. Archaeal lipids in soils and sediments: Water impact and consequences for microbial carbon sequestration
  212. Soil health evaluation approaches along a reclamation consequence in Hangzhou Bay, China
  213. Contrasting effects of maize litter and litter-derived biochar on the temperature sensitivity of paddy soil organic matter decomposition
  214. Biochar induces mineralization of soil recalcitrant components by activation of biochar responsive bacteria groups
  215. Linkages between the temperature sensitivity of soil respiration and microbial life strategy are dependent on sampling season
  216. Metabolic pathways of CO2 fixing microorganisms determined C-fixation rates in grassland soils along the precipitation gradient
  217. Increased microbial biomass and turnover underpin efficient phosphorus acquisition by Brassica chinensis
  218. Microbial iron reduction compensates for phosphorus limitation in paddy soils
  219. Nitrogen transformation genes and ammonia emission from soil under biochar and urease inhibitor application
  220. Physical, chemical and biological subsoiling for sustainable agriculture
  221. Organic Mulching Increases Microbial Activity in Urban Forest Soil
  222. Visualization and quantification of carbon “rusty sink” by rice root iron plaque: Mechanisms, functions, and global implications
  223. Carbon fluxes within tree-crop-grass agroforestry system: 13C field labeling and tracing
  224. Ectomycorrhizal and non‐mycorrhizal rhizosphere fungi increase root‐derived C input to soil and modify enzyme activities: A 14 C pulse labelling of Picea abies seedlings
  225. Effects of plastic film mulch biodegradability on nitrogen in the plant-soil system
  226. Fungal key players of cellulose utilization: Microbial networks in aggregates of long-term fertilized soils disentangled using 13C-DNA-stable isotope probing
  227. Decoupling of soil organic carbon and nutrient mineralization across plant communities as affected by microbial stoichiometry
  228. Divergent responses of aggregate stability to long-term mineral and organic amendments between upland and paddy soils
  229. Soil acidification induced by intensive agricultural use depending on climate
  230. Carbon–Phosphorus Coupling Governs Microbial Effects on Nutrient Acquisition Strategies by Four Crops
  231. Sedge replacement by grasses accelerates litter decomposition and decreases organic matter formation in alpine meadow soils
  232. Increasing contribution of microbial residues to soil organic carbon in grassland restoration chronosequence
  233. Maize root exudate composition alters rhizosphere bacterial community to control hotspots of hydrolase activity in response to nitrogen supply
  234. Microbial community mediates hydroxyl radical production in soil slurries by iron redox transformation
  235. Deep-C storage: Biological, chemical and physical strategies to enhance carbon stocks in agricultural subsoils
  236. Microbial growth rates, carbon use efficiency and enzyme activities during post-agricultural soil restoration
  237. Preface: Arable Land Quality: Observation, Estimation, Optimization, and Application
  238. Nitrite-dependent anaerobic oxidation decreases methane emissions from peatlands
  239. Stoichiometric regulation of priming effects and soil carbon balance by microbial life strategies
  240. Fertilization effects on soil microbial composition and nutrient availability in integrated rice-livestock production systems
  241. Diversified cropping systems benefit soil carbon and nitrogen stocks by increasing aggregate stability: Results of three fractionation methods
  242. Moderate grazing increases newly assimilated carbon allocation belowground
  243. Nutrients in the rhizosphere: A meta-analysis of content, availability, and influencing factors
  244. Vulnerability and driving factors of soil inorganic carbon stocks in Chinese croplands
  245. Nitrogen addition to soil affects microbial carbon use efficiency: Meta‐analysis of similarities and differences in 13 C and 18...
  246. Microbial functional changes mark irreversible course of Tibetan grassland degradation
  247. Phosphorus addition decreases plant lignin but increases microbial necromass contribution to soil organic carbon in a subalpine forest
  248. Can the reductive dissolution of ferric iron in paddy soils compensate phosphorus limitation of rice plants and microorganisms?
  249. Precipitation balances deterministic and stochastic processes of bacterial community assembly in grassland soils
  250. Catalytic efficiency of soil enzymes explains temperature sensitivity: Insights from physiological theory
  251. Network analysis reveals bacterial and fungal keystone taxa involved in straw and soil organic matter mineralization
  252. Low carbon availability in paleosols nonlinearly attenuates temperature sensitivity of soil organic matter decomposition
  253. Initial soil formation by biocrusts: Nitrogen demand and clay protection control microbial necromass accrual and recycling
  254. Plant–microbial competition for amino acids depends on soil acidity and the microbial community
  255. Mediterranean soils under climate change: a drying-rewetting experiment with 14C-labelled glucose
  256. Monoculture vs intercropping under drought: functioning of microorganisms and the fate of maize and soybean 13C-labeled rhizodepositions
  257. Nitrogen deposition in subtropical forest: effect on temperature sensitivity of soil organic matter
  258. Reactive oxygen species in soil: Abiotic mechanisms of biotic processes and consequences for organic matter and nutrient cycling
  259. The size matters: aerobic methane oxidation in thermokarst lake sediments in Western Siberia
  260. Thermokarst lake size controls greenhouse gases production but not its temperature sensitivity
  261. From energy to (soil organic) matter
  262. Initial soil formation by biocrusts: nitrogen demand and clay protection control microbial necromass accrual and recycling
  263. Inter-plant C Transfer and Associations between Plant-assimilated C Inputs and Soil Pores
  264. Nitrogen fertilizers control CO2 emission from calcareous soils: implications for land management and global warming
  265. C:P stoichiometric imbalance between soil and microorganisms drives microbial phosphorus turnover in the rhizosphere
  266. Synergy of saprotrophs with mycorrhiza for litter decomposition and hotspot formation depends on nutrient availability in the rhizosphere
  267. Soil pore architecture and rhizosphere legacy define N2O production in root detritusphere
  268. Increased soil organic matter after 28 years of nitrogen fertilization only with plastic film mulching is controlled by maize root biomass
  269. Three source-partitioning of CO2 fluxes based on a dual-isotope approach to investigate interactions between soil organic carbon, glucose and straw
  270. Investigation of the effects of the conversion of forests and rangeland to cropland on fertility and soil functions in mountainous semi-arid landscape
  271. Paddy soils have a much higher microbial biomass content than upland soils: A review of the origin, mechanisms, and drivers
  272. Rhizosphere bacteriome structure and functions
  273. Depth effects on bacterial community assembly processes in paddy soils
  274. Glycoproteins of arbuscular mycorrhiza for soil carbon sequestration: Review of mechanisms and controls
  275. Plant species and plant neighbor identity affect associations between plant assimilated C inputs and soil pores
  276. Root exudate chemistry affects soil carbon mobilization via microbial community reassembly
  277. A novel belowground in-situ gas labeling approach: CH4 oxidation in deep peat using passive diffusion chambers and 13C excess
  278. Plant and soil elemental C:N:P ratios are linked to soil microbial diversity during grassland restoration on the Loess Plateau, China
  279. From energy to (soil organic) matter
  280. The effect of fertilizer type on nitrogen uptake by maize from recently formed soil organic matter #
  281. Sources and intensity of CH4 production in paddy soils depend on iron oxides and microbial biomass
  282. Effect of long-term fertilisation on enzyme activities and microbial community composition in the rice rhizosphere
  283. Priming effects in soils across Europe
  284. Stimulation of ammonia oxidizer and denitrifier abundances by nitrogen loading: Poor predictability for increased soil N 2 O emission
  285. High frequency of extreme precipitation increases Stipa grandis biomass by altering plant and microbial nitrogen acquisition
  286. Belowground allocation and fate of tree assimilates in plant–soil–microorganisms system: 13C labeling and tracing under field conditions
  287. In-situ 13CO2 labeling to trace carbon fluxes in plant-soil-microorganism systems: Review and methodological guideline
  288. Management extensification in oil palm plantations reduces SOC decomposition
  289. Root and mycorrhizal strategies for nutrient acquisition in forests under nitrogen deposition: A meta-analysis
  290. Regulation of soil phosphorus availability and composition during forest succession in subtropics
  291. Biological Crusts to Increase Soil Carbon Sequestration: New Challenges in a New Environment
  292. Maize genotype-specific exudation strategies: An adaptive mechanism to increase microbial activity in the rhizosphere
  293. Microbial necromass as the source of soil organic carbon in global ecosystems
  294. Arbuscular mycorrhizal fungi and goethite promote carbon sequestration via hyphal-aggregate mineral interactions
  295. Microorganisms maintain C:N stoichiometric balance by regulating the priming effect in long-term fertilized soils
  296. Phosphatase activity and acidification in lupine and maize rhizosphere depend on phosphorus availability and root properties: Coupling zymography with planar optodes
  297. A soil sampling design for arable land quality observation by using SPCOSA–CLHS hybrid approach
  298. Temperature sensitivity of anaerobic methane oxidation versus methanogenesis in paddy soil: Implications for the CH 4 balance under global warming
  299. Molybdenum Bioavailability and Asymbiotic Nitrogen Fixation in Soils are Raised by Iron (Oxyhydr)oxide-Mediated Free Radical Production
  300. Priming effects in the rhizosphere and root detritusphere of two wet-grassland graminoids
  301. Correction to: Tussock microhabitats increase nitrogen uptake by plants in an alpine wetland
  302. Microbial Communities and Functions in the Rhizosphere of Disease-Resistant and Susceptible Camellia spp.
  303. Resistance of microbial community and its functional sensitivity in the rhizosphere hotspots to drought
  304. Long-term warming and elevated CO2 increase ammonia-oxidizing microbial communities and accelerate nitrification in paddy soil
  305. Species richness is more important for ecosystem functioning than species turnover along an elevational gradient
  306. Comparing carbon and nitrogen stocks in paddy and upland soils: Accumulation, stabilization mechanisms, and environmental drivers
  307. Inorganic carbon losses by soil acidification jeopardize global efforts on carbon sequestration and climate change mitigation
  308. Microbial tradeoffs in internal and external use of resources regulated by phosphorus and carbon availability
  309. Rice rhizodeposition promotes the build-up of organic carbon in soil via fungal necromass
  310. Organic matter chemistry and bacterial community structure regulate decomposition processes in post-fire forest soils
  311. Shrubs magnify soil phosphorus depletion in Tibetan meadows: Conclusions from C:N:P stoichiometry and deep soil profiles
  312. Transformations of N derived from straw under long-term conventional and no-tillage soils: A 15N labelling study
  313. The flux of root-derived carbon via fungi and bacteria into soil microarthropods (Collembola) differs markedly between cropping systems
  314. How biochar works, and when it doesn't: A review of mechanisms controlling soil and plant responses to biochar
  315. Forest conversion to plantations: A meta‐analysis of consequences for soil and microbial properties and functions
  316. Rice paddy soils are a quantitatively important carbon store according to a global synthesis
  317. Belowground interplant carbon transfer promotes soil carbon gains in diverse plant communities
  318. Higher free-living N2 fixation at rock-soil interfaces than topsoils during vegetation recovery in karst soils
  319. Plant carbon investment in fine roots and arbuscular mycorrhizal fungi: A cross-biome study on nutrient acquisition strategies
  320. Nitrogen fixation and crop productivity enhancements co‐driven by intercrop root exudates and key rhizosphere bacteria
  321. Annual greenhouse gas emissions from sheepfolds and cattle sheds
  322. Tussock microhabitats increase nitrogen uptake by plants in an alpine wetland
  323. Metagenomic insights into soil microbial communities involved in carbon cycling along an elevation climosequences
  324. Diurnal dynamics can modify plant–microbial competition for N uptake via C allocation
  325. Interkingdom plant-microbial ecological networks under selective and clear cutting of tropical rainforest
  326. δ2H and δ18O in Precipitation and Water Vapor Disentangle Seasonal Wind Directions on the Loess Plateau
  327. Aboveground and Belowground Plant Traits Explain Latitudinal Patterns in Topsoil Fungal Communities From Tropical to Cold Temperate Forests
  328. Root-o-Mat: A novel tool for 2D image processing of root-soil interactions and its application in soil zymography
  329. Time-lapse approach to correct deficiencies of 2D soil zymography
  330. Substrate control of sulphur utilisation and microbial stoichiometry in soil: Results of 13C, 15N, 14C, and 35S quad labelling
  331. Active metabolic pathways of anaerobic methane oxidation in paddy soils
  332. Bacterial communities drive the resistance of soil multifunctionality to land-use change in karst soils
  333. Lower microbial carbon use efficiency reduces cellulose-derived carbon retention in soils amended with compost versus mineral fertilizers
  334. Mitigation of carbon dioxide by accelerated sequestration from long-term biochar amended paddy soil
  335. Post-agricultural restoration of soil organic carbon pools across a climate gradient
  336. Soil organic matter formation is controlled by the chemistry and bioavailability of organic carbon inputs across different land uses
  337. Stoichiometry of carbon, nitrogen, and phosphorus in soil: Effects of agricultural land use and climate at a continental scale
  338. T4-like Phages Reveal the Potential Role of Viruses in Soil Organic Matter Mineralization
  339. From rock eating to vegetarian ecosystems — Disentangling processes of phosphorus acquisition across biomes
  340. Accumulation of organic compounds in paddy soils after biochar application is controlled by iron hydroxides
  341. Fertilization effects on microbial community composition and aggregate formation in saline‐alkaline soil
  342. Temperature sensitivity of SOM decomposition is linked with a K‐selected microbial community
  343. Rhizosphere microbiome modulated effects of biochar on ryegrass 15N uptake and rhizodeposited 13C allocation in soil
  344. Contrasting pathways of carbon sequestration in paddy and upland soils
  345. Microbiome of the Rhizosphere: from Structure to Functions
  346. An Approach to Incorporate Rhizosphere Priming Effect into Soil Organic Matter Models
  347. Decomposing in-situ grown switchgrass roots as hotspots of microbial activity and N2O emission: the combination of dual-isotope labeling and zymography
  348. Contribution of the Fenton reaction and ligninolytic enzymes to soil organic matter mineralisation under anoxic conditions
  349. Drought effects on soil carbon and nitrogen dynamics in global natural ecosystems
  350. Fenton chemistry and reactive oxygen species in soil: Abiotic mechanisms of biotic processes, controls and consequences for carbon and nutrient cycling
  351. Iron-reducing bacteria decompose lignin by electron transfer from soil organic matter
  352. Soil properties and root traits jointly shape fine-scale spatial patterns of bacterial community and metabolic functions within a Korean pine forest
  353. Microbial metabolic response to winter warming stabilizes soil carbon
  354. Soil carbonates: The unaccounted, irrecoverable carbon source
  355. Letter-to-the-Editor: Does acidification really increase soil carbon in croplands? How statistical analyses of large datasets might mislead the conclusions
  356. Spartina alterniflora invasion controls organic carbon stocks in coastal marsh and mangrove soils across tropics and subtropics
  357. The δ13C, δ18O and Δ47 records in biogenic, pedogenic and geogenic carbonate types from paleosol-loess sequence and their paleoenvironmental meaning
  358. Riparian wetland properties counter the effect of land-use change on soil carbon stocks after rainforest conversion to plantations
  359. Increase of soil nitrogen availability and recycling with stand age of Chinese-fir plantations
  360. Strong priming of soil organic matter induced by frequent input of labile carbon
  361. Temperature sensitivity (Q) of stable, primed and easily available organic matter pools during decomposition in paddy soil
  362. Facts to acidification‐induced carbonate losses from Chinese croplands
  363. Soil organic matter turnover depending on land use change: Coupling C/N ratios, δ 13 C, and lignin biomarkers
  364. Plant intraspecific competition and growth stage alter carbon and nitrogen mineralization in the rhizosphere
  365. Impact of manure on soil biochemical properties: A global synthesis
  366. Conversion of cropland to natural vegetation boosts microbial and enzyme activities in soil
  367. Decreased rhizodeposition, but increased microbial carbon stabilization with soil depth down to 3.6 m
  368. Effects of rotational and continuous overgrazing on newly assimilated C allocation
  369. Tight coupling of fungal community composition with soil quality in a Chinese fir plantation chronosequence
  370. Long‐term active restoration of extremely degraded alpine grassland accelerated turnover and increased stability of soil carbon
  371. An iron-dependent burst of hydroxyl radicals stimulates straw decomposition and CO2 emission from soil hotspots: Consequences of Fenton or Fenton-like reactions
  372. Meta-analysis of heavy metal effects on soil enzyme activities
  373. 15N-tracer approach to assess nitrogen cycling processes: Nitrate reduction, anammox and denitrification in different pH cropland soils
  374. Soil phosphorus accumulation changes with decreasing temperature along a 2300 m altitude gradient
  375. Organic matter stabilization in aggregates and density fractions in paddy soil depending on long-term fertilization: Tracing of pathways by 13C natural abundance
  376. Assessing and mapping urban soils as geochemical barriers for contamination by heavy metal(loid)s in Moscow megapolis
  377. Nitrogen rhizodeposition by legumes and its fate in agroecosystems: A field study and literature review
  378. Divergent mineralization of hydrophilic and hydrophobic organic substrates and their priming effect in soils depending on their preferential utilization by bacteria and fungi
  379. Combined biochar and nitrogen application stimulates enzyme activity and root plasticity
  380. Corrigendum to “Accelerated microbial activity, turnover and efficiency in the drilosphere is depth dependent” [Soil Biology & Biochemistry 147 (2020) 107852]
  381. The effect of microorganisms on soil carbonate recrystallization and abiotic CO2 uptake of soil
  382. Pore‐scale view of microbial turnover: Combining 14 C imaging, μCT and zymography after adding soluble carbon to soil pores of specific sizes
  383. Accelerated microbial activity, turnover and efficiency in the drilosphere is depth dependent
  384. Rusty sink of rhizodeposits and associated keystone microbiomes
  385. Synergy effect of peroxidase enzymes and Fenton reactions greatly increase the anaerobic oxidation of soil organic matter
  386. Differentiating microbial taxonomic and functional responses to physical disturbance in bulk and rhizosphere soils
  387. Compositional variations of active autotrophic bacteria in paddy soils with elevated CO2 and temperature
  388. Soil quality indices for metal(loid) contamination: An enzymatic perspective
  389. Contrasting patterns and drivers of soil bacterial and fungal diversity across a mountain gradient
  390. Corrigendum to “Microbial carbon use efficiency, biomass turnover, and necromass accumulation in paddy soil depending on fertilization” [Agric. Ecosyst. Environ. 292 April (2020) 106816]
  391. Responses of C-, N- and P-acquiring hydrolases to P and N fertilizers in a subtropical Chinese fir plantation depend on soil depth
  392. Secondary soil salinization in urban lawns: Microbial functioning, vegetation state, and implications for carbon balance
  393. Effects of drying/rewetting on soil aggregate dynamics and implications for organic matter turnover
  394. Soil-plant co-stimulation during forest vegetation restoration in a subtropical area of southern China
  395. Nutrient addition reduces carbon sequestration in a Tibetan grassland soil: Disentangling microbial and physical controls
  396. Dramatic loss of inorganic carbon by nitrogen‐induced soil acidification in Chinese croplands
  397. Organic carbon burial and sources in soils of coastal mudflat and mangrove ecosystems
  398. Microbial carbon use efficiency, biomass turnover, and necromass accumulation in paddy soil depending on fertilization
  399. C:N stoichiometry of stable and labile organic compounds determine priming patterns
  400. Can combined application of biochar and nitrogen promote microbial functions and root plasticity for plant growth in low-fertile soils?
  401. Carbon flows by soil organic matter formation: A review based on 13C natural abundance
  402. Combined application of manure and mineral fertilizers weakens the impact of manure on soil biochemical properties
  403. How 'hot' are the hotspots: Statistical approach to localize the high activity areas on soil images
  404. Iron-reducing bacteria play a key role in lignin degradation by electron transferring from soil organic matter
  405. Loss of available soil organic carbon from afforestation plots: effect of tree species composition and warming
  406. Rhizosphere hotspots: root hairs and warming control microbial efficiency, carbon utilization and energy production
  407. Soil carbon dynamic after freezing/thawing and drying/wetting in a temperate forest soil: Dual labeling of 13C and 14C
  408. Soil organic matter formation: Convergence and divergence of three carbon pathways: Stabilization, recycling and losses
  409. DNA Stable-Isotope Probing Delineates Carbon Flows from Rice Residues into Soil Microbial Communities Depending on Fertilization
  410. C:N stoichiometry of stable and labile organic compounds determine priming patterns
  411. Carbon and nitrogen recycling from microbial necromass to cope with C:N stoichiometric imbalance by priming
  412. Effects of land use and elevation on the functional characteristics of soil enzymes at Mt. Kilimanjaro
  413. In situ methods of plant-microbial interactions for nitrogen in rhizosphere
  414. Anaerobic oxidation of methane in paddy soil: Role of electron acceptors and fertilization in mitigating CH4 fluxes
  415. Biochar effects on crop yields and nitrogen loss depending on fertilization
  416. Corrigendum to “Biochar effects on crop yields and nitrogen loss depending on fertilization” [Sci. Total Environ. 702 (2020) 134423]
  417. Divergence in fungal abundance and community structure between soils under long-term mineral and organic fertilization
  418. Conversion of coastal marshes to croplands decreases organic carbon but increases inorganic carbon in saline soils
  419. Arbuscular mycorrhiza enhances rhizodeposition and reduces the rhizosphere priming effect on the decomposition of soil organic matter
  420. Direct evidence for thickening nanoscale organic films at soil biogeochemical interfaces and its relevance to organic matter preservation
  421. Effects of six-year biochar amendment on soil aggregation, crop growth, and nitrogen and phosphorus use efficiencies in a rice-wheat rotation
  422. Changes in the Fractional Composition of Organic Matter in the Soils of the Forest–Steppe Zone during Their Postagrogenic Evolution
  423. Reviews and syntheses: Agropedogenesis – humankind as the sixth soil-forming factor and attractors of agricultural soil degradation
  424. Temperature sensitivity of soil organic matter mineralization decreases with long‐term N fertilization: Evidence from four Q 10 estimation approaches
  425. Persistence of soil microbial function at the rock‐soil interface in degraded karst topsoils
  426. Bacterial community succession in paddy soil depending on rice fertilization
  427. Nitrogen fertilization modifies organic transformations and coatings on soil biogeochemical interfaces through microbial polysaccharides synthesis
  428. Regulation of priming effect by soil organic matter stability over a broad geographic scale
  429. TEMPERATURE SENSITIVITY OF DECOMPOSITION OF SOIL ORGANIC MATTER FRACTIONS INCREASES WITH THEIR TURNOVER TIME
  430. Reduced tillage and increased residue retention increase enzyme activity and carbon and nitrogen concentrations in soil particle size fractions in a long-term field experiment on Loess Plateau in China
  431. Mechanisms of carbon sequestration and stabilization by restoration of arable soils after abandonment: A chronosequence study on Phaeozems and Chernozems
  432. Soil Phosphorus Bioavailability and Recycling Increased with Stand Age in Chinese Fir Plantations
  433. Fate of phosphorus fertilizer in acidic Cambisol assessed using 33P isotope labeling technique
  434. Vegetation restoration stimulates soil carbon sequestration and stabilization in a subtropical area of southern China
  435. Labile organic matter intensifies phosphorous mobilization in paddy soils by microbial iron (III) reduction
  436. MgO-modified biochar increases phosphate retention and rice yields in saline-alkaline soil
  437. Post-agricultural restoration: Implications for dynamics of soil organic matter pools
  438. Root trait plasticity and plant nutrient acquisition in phosphorus limited soil
  439. Author Correction: Microbial spatial footprint as a driver of soil carbon stabilization
  440. Ashes to ashes: Characterization of organic matter in Andosols along a 3400 m elevation transect at Mount Kilimanjaro using analytical pyrolysis
  441. Saving the face of soil aggregates
  442. Impact of sea level change on coastal soil organic matter, priming effects and prokaryotic community assembly
  443. Coupling zymography with pH mapping reveals a shift in lupine phosphorus acquisition strategy driven by cluster roots
  444. Rhizosphere size and shape: Temporal dynamics and spatial stationarity
  445. Long‐term nitrogen addition modifies microbial composition and functions for slow carbon cycling and increased sequestration in tropical forest soil
  446. Labile carbon matters more than temperature for enzyme activity in paddy soil
  447. Soil organic matter priming and carbon balance after straw addition is regulated by long-term fertilization
  448. Spatial patterns of extracellular enzymes: Combining X-ray computed micro-tomography and 2D zymography
  449. Transpiration on the rebound in lowland Sumatra
  450. Recovery of organic matter and microbial biomass after abandonment of degraded agricultural soils: the influence of climate
  451. Drivers of soil carbon stabilization in oil palm plantations
  452. Inventory of Spatio-Temporal Methane Emissions from Livestock and Poultry Farming in Beijing
  453. Microbial spatial footprint as a driver of soil carbon stabilization
  454. Effects of peat decomposition on δ13C and δ15N depth profiles of Alpine bogs
  455. Long-term manure application increases soil organic matter and aggregation, and alters microbial community structure and keystone taxa
  456. Manure over crop residues increases soil organic matter but decreases microbial necromass relative contribution in upland Ultisols: Results of a 27-year field experiment
  457. Straw and biochar strongly affect functional diversity of microbial metabolism in paddy soils
  458. Integrating Aquatic and Terrestrial Perspectives to Improve Insights Into Organic Matter Cycling at the Landscape Scale
  459. Spatial pattern of enzyme activities depends on root exudate composition
  460. To shake or not to shake: 13C-based evidence on anaerobic methane oxidation in paddy soil
  461. When the Mediterranean becomes harsh: Heat pulses strongly affect C allocation in plant-soil-atmosphere continuum in Eucalyptus camaldulensis
  462. Afforestation of loess soils: Old and new organic carbon in aggregates and density fractions
  463. Carbon input and allocation by rice into paddy soils: A review
  464. Dominant extracellular enzymes in priming of SOM decomposition depend on temperature
  465. Impacts of green manure amendment on detritus micro-food web in a double-rice cropping system
  466. Regulation of soil phosphorus cycling in grasslands by shrubs
  467. Nitrogen-inputs regulate microbial functional and genetic resistance and resilience to drying–rewetting cycles, with implications for crop yields
  468. Contrasting patterns and drivers of soil fungal communities in subtropical deciduous and evergreen broadleaved forests
  469. Agropedogenesis: Humankind as the 6<sup>th</sup> soil-forming factor and attractors of agrogenic soil degradation
  470. Supplementary material to "Agropedogenesis: Humankind as the 6<sup>th</sup> soil-forming factor and attractors of agrogenic soil degradation"
  471. Understory ferns alter soil carbon chemistry and increase carbon storage during reforestation with native pine on previously degraded sites
  472. Functional Soil Organic Matter Fractions, Microbial Community, and Enzyme Activities in a Mollisol Under 35 Years Manure and Mineral Fertilization
  473. Glucose and ribose stabilization in soil: Convergence and divergence of carbon pathways assessed by position-specific labeling
  474. Microbial C:N:P stoichiometry and turnover depend on nutrients availability in soil: A 14C, 15N and 33P triple labelling study
  475. Phenological Stage, Plant Biomass, and Drought Stress Affect Microbial Biomass and Enzyme Activities in the Rhizosphere of Enteropogon macrostachyus
  476. Extreme-duration drought impacts on soil CO2 efflux are regulated by plant species composition
  477. Climate–land-use interactions shape tropical mountain biodiversity and ecosystem functions
  478. Effect of nitrogen fertilizer on rice photosynthate allocation and Carbon input in paddy soil
  479. Priming alters soil carbon dynamics during forest succession
  480. Calibration of 2-D soil zymography for correct analysis of enzyme distribution
  481. Environmental drivers and stoichiometric constraints on enzyme activities in soils from rhizosphere to continental scale
  482. Initial utilization of rhizodeposits with rice growth in paddy soils: Rhizosphere and N fertilization effects
  483. Fate and transport of urea-N in a rain-fed ridge-furrow crop system with plastic mulch
  484. Intensified Precipitation Seasonality Reduces Soil Inorganic N Content in a Subtropical Forest: Greater Contribution of Leaching Loss Than N 2 O Emissions
  485. Structural and physiological adaptations of soil microorganisms to freezing revealed by position-specific labeling and compound-specific 13C analysis
  486. To shake or not to shake: Silicone tube approach for incubation studies on CH4 oxidation in submerged soils
  487. Tree species identity surpasses richness in affecting soil microbial richness and community composition in subtropical forests
  488. Allocation of assimilated carbon in paddies depending on rice age, chase period and N fertilization: Experiment with 13CO2 labelling and literature synthesis
  489. Visualization and quantification of root exudation using 14C imaging: challenges and uncertainties
  490. Nitrogen and phosphorus enrichment accelerates soil organic carbon loss in alpine grassland on the Qinghai-Tibetan Plateau
  491. C/P stoichiometry of dying rice root defines the spatial distribution and dynamics of enzyme activities in root-detritusphere
  492. Ferrous Wheel Hypothesis: Abiotic nitrate incorporation into dissolved organic matter
  493. Review and synthesis of the effects of elevated atmospheric CO2 on soil processes: No changes in pools, but increased fluxes and accelerated cycles
  494. The Kobresia pygmaea ecosystem of the Tibetan highlands – Origin, functioning and degradation of the world's largest pastoral alpine ecosystem
  495. Easily mineralizable carbon in manure-based biochar added to a soil influences N2 O emissions and microbial-N cycling genes
  496. Alteration process during the post-agricultural restoration of Luvisols of the temperate broad-leaved forest in Russia
  497. Quantitative soil zymography: Mechanisms, processes of substrate and enzyme diffusion in porous media
  498. Viruses in soil: Nano-scale undead drivers of microbial life, biogeochemical turnover and ecosystem functions
  499. Warming exerts greater impacts on subsoil than topsoil CO2 efflux in a subtropical forest
  500. Contribution of soil inorganic carbon to atmospheric CO 2 : More important than previously thought
  501. Metabolic tracing unravels pathways of fungal and bacterial amino sugar formation in soil
  502. Carbon and nitrogen availability in paddy soil affects rice photosynthate allocation, microbial community composition, and priming: combining continuous 13C labeling with PLFA analysis
  503. Manure and Mineral Fertilizer Effects on Crop Yield and Soil Carbon Sequestration: A Meta‐Analysis and Modeling Across China
  504. Interactive priming effect of labile carbon and crop residues on SOM depends on residue decomposition stage: Three-source partitioning to evaluate mechanisms
  505. Chemistry and microbiology of the Critical Zone along a steep climate and vegetation gradient in the Chilean Coastal Cordillera
  506. Pedogenic and microbial interrelations to regional climate and local topography: New insights from a climate gradient (arid to humid) along the Coastal Cordillera of Chile
  507. Correction to: Simulated leaf litter addition causes opposite priming effects on natural forest and plantation soils
  508. Simulated leaf litter addition causes opposite priming effects on natural forest and plantation soils
  509. Microbial processing of plant residues in the subsoil – The role of biopores
  510. Isolating organic carbon fractions with varying turnover rates in temperate agricultural soils – A comprehensive method comparison
  511. Agroforestry systems: Meta-analysis of soil carbon stocks, sequestration processes, and future potentials
  512. Contrasting effects of organic and mineral nitrogen challenge the N-Mining Hypothesis for soil organic matter priming
  513. Effects of rhizosphere wettability on microbial biomass, enzyme activities and localization
  514. Incorporation of rice straw carbon into dissolved organic matter and microbial biomass along a 100-year paddy soil chronosequence
  515. Carbon allocation and fate in paddy soil depending on phosphorus fertilization and water management: results of 13C continuous labelling of rice
  516. Land Degradation & Development : A new and bright future
  517. Spatiotemporal patterns of enzyme activities in the rhizosphere: effects of plant growth and root morphology
  518. Deforestation decreases spatial turnover and alters the network interactions in soil bacterial communities
  519. Depth rather than microrelief controls microbial biomass and kinetics of C-, N-, P- and S-cycle enzymes in peatland
  520. Conversion of Tibetan grasslands to croplands decreases accumulation of microbially synthesized compounds in soil
  521. Ash and fire, char, and biochar in the environment
  522. Spatial heterogeneity of microbial community and enzyme activities in a broad-leaved Korean pine mixed forest
  523. Carbon budgets of top- and subsoil food webs in an arable system
  524. Carbon costs and benefits of Indonesian rainforest conversion to plantations
  525. Priming effects induced by glucose and decaying plant residues on SOM decomposition: A three-source 13C/14C partitioning study
  526. Carbon budget and greenhouse gas balance during the initial years after rice paddy conversion to vegetable cultivation
  527. Effects of rain shortage on carbon allocation, pools and fluxes in a Mediterranean shrub ecosystem – a 13C labelling field study
  528. Responses of Soil Enzyme Activities and Microbial Community Composition to Moisture Regimes in Paddy Soils Under Long-Term Fertilization Practices
  529. Global-change effects on early-stage decomposition processes in tidal wetlands – implications from a global survey using standardized litter
  530. Teatime on Mount Kilimanjaro: Assessing climate and land-use effects on litter decomposition and stabilization using the Tea Bag Index
  531. Effect of biochar origin and soil pH on greenhouse gas emissions from sandy and clay soils
  532. Carbon and nitrogen mineralization and enzyme activities in soil aggregate-size classes: Effects of biochar, oyster shells, and polymers
  533. Phosphorus fractions in subtropical soils depending on land use
  534. Land use and fertilisation affect priming in tropical andosols
  535. Long-term effects of nitrogen fertilization on aggregation and localization of carbon, nitrogen and microbial activities in soil
  536. Towards a conversion factor for soil microbial phosphorus
  537. Urban soils as hot spots of anthropogenic carbon accumulation: Review of stocks, mechanisms and driving factors
  538. Nitrogen pools and cycles in Tibetan Kobresia pastures depending on grazing
  539. Nitrogen fertilization raises CO2 efflux from inorganic carbon: A global assessment
  540. Maize phenology alters the distribution of enzyme activities in soil: Field estimates
  541. Responses of Soil Enzyme Activities and Microbial Community Composition to Moisture Regimes in Paddy Soils Under Long-Term Fertilization Practices
  542. Tibetan sedges sequester more carbon belowground than grasses: a 13C labeling study
  543. DNA-based determination of soil microbial biomass in alkaline and carbonaceous soils of semi-arid climate
  544. Functional soil organic matter fractions in response to long-term fertilization in upland and paddy systems in South China
  545. Spatial patterns of enzyme activities in the rhizosphere: Effects of root hairs and root radius
  546. Feedstock determines biochar-induced soil priming effects by stimulating the activity of specific microorganisms
  547. Food for microorganisms: Position-specific 13 C labeling and 13 C-PLFA analysis reveals preferences for sorbed or necromass C
  548. Shift from dormancy to microbial growth revealed by RNA:DNA ratio
  549. Effects of biotic and abiotic factors on soil organic matter mineralization: Experiments and structural modeling analysis
  550. Degradation of Tibetan grasslands: Consequences for carbon and nutrient cycles
  551. Rice rhizodeposits affect organic matter priming in paddy soil: The role of N fertilization and plant growth for enzyme activities, CO 2 and CH 4 emissions
  552. Soil microorganisms exhibit enzymatic and priming response to root mucilage under drought
  553. Effects of Elevated CO2 in the Atmosphere on Soil C and N Turnover
  554. The Potential for Soils to Mitigate Climate Change Through Carbon Sequestration
  555. Impact of forest fire on soil properties (review)
  556. Root hairs increase rhizosphere extension and carbon input to soil
  557. Global change effects on decomposition processes in tidal wetlands: implications from a global survey using standardized litter
  558. Rhizodeposition under drought is controlled by root growth rate and rhizosphere water content
  559. Supplementary material to "Global change effects on decomposition processes in tidal wetlands: implications from a global survey using standardized litter"
  560. Mapping the footprint of nematodes in the rhizosphere: Cluster root formation and spatial distribution of enzyme activities
  561. Carbon sequestration and turnover in soil under the energy crop Miscanthus : repeated 13 C natural abundance approach and literature synthesis
  562. Comments to Bastos et al. Land-use change vs. climate variability in 1940s ... from Anonymous Reviewer
  563. Anonymous Reviewer Comments
  564. Comments to Bastos et al. Land-use change vs. climate variability in 1940s ...
  565. Effects of maize roots on aggregate stability and enzyme activities in soil
  566. Effects of flooding on phosphorus and iron mobilization in highly weathered soils under different land-use types: Short-term effects and mechanisms
  567. Rolling in the deep: Priming effects in earthworm biopores in topsoil and subsoil
  568. Shifts in microbial communities with increasing soil fertility across a chronosequence of paddy cultivation in subtropical China
  569. Six months of L. terrestris L. activity in root-formed biopores increases nutrient availability, microbial biomass and enzyme activity
  570. Weaker priming and mineralisation of low molecular weight organic substances in paddy than in upland soil
  571. Decrease of soil organic matter stabilization with increasing inputs: Mechanisms and controls
  572. Preface: Special issue SOM 2015
  573. Stability and dynamics of enzyme activity patterns in the rice rhizosphere: Effects of plant growth and temperature
  574. Soil Organic Carbon in a Changing World
  575. Carbon input by roots into the soil: Quantification of rhizodeposition from root to ecosystem scale
  576. Soil organic matter availability and climate drive latitudinal patterns in bacterial diversity from tropical to cold temperate forests
  577. Spatio-temporal patterns of enzyme activities after manure application reflect mechanisms of niche differentiation between plants and microorganisms
  578. Does long-term warming affect C and N allocation in a Mediterranean shrubland ecosystem? Evidence from a 13C and 15N labeling field study
  579. Nitrogen fertilization decreases the decomposition of soil organic matter and plant residues in planted soils
  580. Contrasting responses of phosphatase kinetic parameters to nitrogen and phosphorus additions in forest soils
  581. Beech trees fuel soil animal food webs via root-derived nitrogen
  582. Hydrolase kinetics to detect temperature-related changes in the rates of soil organic matter decomposition
  583. The tree species matters: Belowground carbon input and utilization in the myco-rhizosphere
  584. Different responses of ash and beech on nitrate versus ammonium leaf labeling
  585. Rhizosphere engineering: Innovative improvement of root environment
  586. Labile carbon and nitrogen additions affect soil organic matter decomposition more strongly than temperature
  587. Microbial Metabolism in Soil at Subzero Temperatures: Adaptation Mechanisms Revealed by Position-Specific 13C Labeling
  588. Community-weighted means and functional dispersion of plant functional traits along environmental gradients on Mount Kilimanjaro
  589. Responses of Degraded TibetanKobresiaPastures to N Addition
  590. Soil nitrogen transformation responses to seasonal precipitation changes are regulated by changes in functional microbial abundance in a subtropical forest
  591. Labelling plants in the Chernobyl way: A new 137Cs and 14C foliar application approach to investigate rhizodeposition and biopore reuse
  592. CH4 and CO2 production below two contrasting peatland micro-relief forms: An inhibitor and δ13C study
  593. Effect of land use and management practices on microbial biomass and enzyme activities in subtropical top-and sub-soils
  594. Does repeated biochar incorporation induce further soil priming effect?
  595. Biopore history determines the microbial community composition in subsoil hotspots
  596. “Non-metabolizable” glucose analogue shines new light on priming mechanisms: Triggering of microbial metabolism
  597. Annual methane uptake from different land uses in an agro-pastoral ecotone of northern China
  598. Response of soil organic matter fractions and composition of microbial community to long-term organic and mineral fertilization
  599. Sorption of Alanine changes microbial metabolism in addition to availability
  600. Warming increases hotspot areas of enzyme activity and shortens the duration of hot moments in the root-detritusphere
  601. Nitrogen fertilization increases rhizodeposit incorporation into microbial biomass and reduces soil organic matter losses
  602. Effects of grazing on the acquisition of nitrogen by plants and microorganisms in an alpine grassland on the Tibetan plateau
  603. Priming effects in biochar enriched soils using a three-source-partitioning approach: 14C labelling and 13C natural abundance
  604. Microbial uptake and utilization of low molecular weight organic substrates in soil depend on carbon oxidation state
  605. Soil aggregation regulates distributions of carbon, microbial community and enzyme activities after 23-year manure amendment
  606. Comments to your ms
  607. Soil microorganisms can overcome respiration inhibition by coupling intra- and extracellular metabolism: 13C metabolic tracing reveals the mechanisms
  608. Hot experience for cold-adapted microorganisms: Temperature sensitivity of soil enzymes
  609. Land-use change affects phosphorus fractions in highly weathered tropical soils
  610. Carbon Sources in Fruit Carbonate of Buglossoides arvensis and Consequences for 14C Dating
  611. Extreme rainfall and snowfall alter soil respiration
  612. Soil nitrogen transformation responses to seasonal precipitation changes are regulated by changes in functional microbial abundance in a subtropical forest
  613. Supplementary material to "Soil nitrogen transformation responses to seasonal precipitation changes are regulated by changes in functional microbial abundance in a subtropical forest"
  614. Decadal Nitrogen Fertilization Decreases Mineral-Associated and Subsoil Carbon: A 32-Year Study
  615. Turnover of microbial groups and cell components in soil: <sup>13</sup>C analysis of cellular biomarkers
  616. Mineralization of “non-metabolizable” glucose analogues in soil: potential chemosensory mimics of glucose
  617. Microbial decomposition of soil organic matter is mediated by quality and quantity of crop residues: mechanisms and thresholds
  618. Interactions between biochar and litter priming: A three-source 14 C and δ 13 C partitioning study
  619. Visualization of Enzyme Activities in Earthworm Biopores by In Situ Soil Zymography
  620. Rapid decrease of soil carbon after abandonment of subtropical paddy fields
  621. Legume and Non-legume Trees Increase Soil Carbon Sequestration in Savanna
  622. Enzyme properties down the soil profile - A matter of substrate quality in rhizosphere and detritusphere
  623. Fluxes of root-derived carbon into the nematode micro-food web of an arable soil
  624. Functional response of soil microbial communities to tillage, cover crops and nitrogen fertilization
  625. How do microbial communities in top- and subsoil respond to root litter addition under field conditions?
  626. Incorporation of root C and fertilizer N into the food web of an arable field: Variations with functional group and energy channel
  627. N fertilization decreases soil organic matter decomposition in the rhizosphere
  628. Forest vegetation in western Romania in relation to climate variables: Does community composition reflect modelled tree species distribution?
  629. Recrystallization of shell carbonate in soil: 14C labeling, modeling and relevance for dating and paleo-reconstructions
  630. CaCO 3 recrystallization in saline and alkaline soils
  631. Rice rhizodeposition and its utilization by microbial groups depends on N fertilization
  632. Interactive effects of biochar and polyacrylamide on decomposition of maize rhizodeposits: implications from 14C labeling and microbial metabolic quotient
  633. Response of soil microbial community to afforestation with pure and mixed species
  634. Drying-rewetting cycles alter carbon and nitrogen mineralization in litter-amended alpine wetland soil
  635. Hotspots of microbial activity induced by earthworm burrows, old root channels, and their combination in subsoil
  636. Soil degradation in oil palm and rubber plantations under land resource scarcity
  637. Carbon budget by priming in a biochar-amended soil
  638. Effects of nitrate and sulfate on greenhouse gas emission potentials from microform-derived peats of a boreal peatland: A 13 C tracer study
  639. Rhizosphere priming of barley with and without root hairs
  640. Nitrogen turnover and greenhouse gas emissions in a tropical alpine ecosystem, Mt. Kilimanjaro, Tanzania
  641. Belowground carbon allocation and dynamics under rice cultivation depends on soil organic matter content
  642. Fate of Organic and Inorganic Nitrogen in Crusted and Non‐Crusted Kobresia Grasslands
  643. Earthworm burrows: Kinetics and spatial distribution of enzymes of C-, N- and P- cycles
  644. Sensitivity and resistance of soil fertility indicators to land-use changes: New concept and examples from conversion of Indonesian rainforest to plantations
  645. The above-belowground coupling of the C cycle: fast and slow mechanisms of C transfer for root and rhizomicrobial respiration
  646. Cation exchange retards shell carbonate recrystallization: consequences for dating and paleoenvironmental reconstructions
  647. Dissolved and colloidal phosphorus fluxes in forest ecosystems-an almost blind spot in ecosystem research
  648. Maize rhizosphere priming: field estimates using 13C natural abundance
  649. Carbon turnover in cell compartments and microbial groups in soil
  650. Land use affects soil biochemical properties in Mt. Kilimanjaro region
  651. Pedogenic carbonates: Forms and formation processes
  652. Aggregate size and glucose level affect priming sources: A three-source-partitioning study
  653. Biochar affects soil organic matter cycling and microbial functions but does not alter microbial community structure in a paddy soil
  654. Biochar has no effect on soil respiration across Chinese agricultural soils
  655. Iron oxidation affects nitrous oxide emissions via donating electrons to denitrification in paddy soils
  656. Temperature selects for static soil enzyme systems to maintain high catalytic efficiency
  657. Microtopography matters for CH4 formation in a peat soil: a combined inhibitor and 13C study
  658. Carbon and Nitrogen Losses from Soil Depend on Degradation of Tibetan Kobresia Pastures
  659. Rhizosphere shape of lentil and maize: Spatial distribution of enzyme activities
  660. Allocation and dynamics of C and N within plant-soil system of ash and beech
  661. Lasting effect of soil warming on organic matter decomposition depends on tillage practices
  662. Carbon input and partitioning in subsoil by chicory and alfalfa
  663. Nitrogen acquisition by plants and microorganisms in a temperate grassland
  664. Microbial utilization of rice root exudates: 13C labeling and PLFA composition
  665. Suppression of soil organic matter decomposition by gasoline and diesel as assessed by 13C natural abundance
  666. Temperature sensitivity and enzymatic mechanisms of soil organic matter decomposition along an altitudinal gradient on Mount Kilimanjaro
  667. Effects of biochar and polyacrylamide on decomposition of soil organic matter and 14C-labeled alfalfa residues
  668. Spatial distribution and catalytic mechanisms of β-glucosidase activity at the root-soil interface
  669. Direct incorporation of fatty acids into microbial phospholipids in soils: Position-specific labeling tells the story
  670. Carbon and nitrogen additions induce distinct priming effects along an organic-matter decay continuum
  671. Neoformation of pedogenic carbonates by irrigation and fertilization and their contribution to carbon sequestration in soil
  672. Substrate quality affects kinetics and catalytic efficiency of exo-enzymes in rhizosphere and detritusphere
  673. Water scarcity and oil palm expansion: social views and environmental processes
  674. Substrate quality affects microbial- and enzyme activities in rooted soil
  675. Nitrous oxide emissions from an agro-pastoral ecotone of northern China depending on land uses
  676. Gross Nitrogen Dynamics in the Mycorrhizosphere of an Organic Forest Soil
  677. Sugars in soil and sweets for microorganisms: Review of origin, content, composition and fate
  678. Root Effects on Soil Organic Matter Decomposition
  679. Nonlinear temperature sensitivity of enzyme kinetics explains canceling effect—a case study on loamy haplic Luvisol
  680. Annual litterfall dynamics and nutrient deposition depending on elevation and land use at Mt. Kilimanjaro
  681. Large-scale carbon sequestration in post-agrogenic ecosystems in Russia and Kazakhstan
  682. The effect of plastic mulch on the fate of urea-N in rain-fed maize production in a semiarid environment as assessed by 15N-labeling
  683. Allocation of freshly assimilated carbon into primary and secondary metabolites after in situ13C pulse labelling of Norway spruce (Picea abies)
  684. Biochars and the plant-soil interface
  685. Loss of labile organic carbon from subsoil due to land-use changes in subtropical China
  686. Organic nitrogen uptake by plants: reevaluation by position-specific labeling of amino acids
  687. Small but active - pool size does not matter for carbon incorporation in below-ground food webs
  688. Land Use and Precipitation Affect Organic and Microbial Carbon Stocks and the Specific Metabolic Quotient in Soils of Eleven Ecosystems of Mt. Kilimanjaro, Tanzania
  689. Effects of biochar amendment on greenhouse gas emissions, net ecosystem carbon budget and properties of an acidic soil under intensive vegetable production
  690. Contrasting effects of aged and fresh biochars on glucose-induced priming and microbial activities in paddy soil
  691. Microbial and enzymes response to nutrient additions in soils of Mt. Kilimanjaro region depending on land use
  692. Biochar stability in soil: meta-analysis of decomposition and priming effects
  693. Land use change decreases soil carbon stocks in Tibetan grasslands
  694. Aggregate size and their disruption affect 14C-labeled glucose mineralization and priming effect
  695. Root-Derived Short-Chain Suberin Diacids from Rice and Rape Seed in a Paddy Soil under Rice Cultivar Treatments
  696. Nitrogen Uptake in an Alpine Kobresia Pasture on the Tibetan Plateau: Localization by 15N Labeling and Implications for a Vulnerable Ecosystem
  697. Losses of soil carbon by converting tropical forest to plantations: erosion and decomposition estimated byδ13C
  698. Microbial hotspots and hot moments in soil: Concept & review
  699. Oxygen and redox potential gradients in the rhizosphere of alfalfa grown on a loamy soil
  700. Carbon pools and fluxes in a Tibetan alpine Kobresia pygmaea pasture partitioned by coupled eddy-covariance measurements and 13CO2 pulse labeling
  701. Assessing the stability of soil organic matter by fractionation and 13C isotope techniques
  702. Partitioning NEE for absolute C input into various ecosystem pools by combining results from eddy-covariance, atmospheric flux partitioning and 13CO2 pulse labeling
  703. Biochemistry of hexose and pentose transformations in soil analyzed by position-specific labeling and 13C-PLFA
  704. Linkages between the soil organic matter fractions and the microbial metabolic functional diversity within a broad-leaved Korean pine forest
  705. Pasture degradation modifies the water and carbon cycles of the Tibetan highlands
  706. Dynamics of soil organic carbon pools after agricultural abandonment
  707. Effect of plant communities on aggregate composition and organic matter stabilisation in young soils
  708. Fate of low molecular weight organic substances in an arable soil: From microbial uptake to utilisation and stabilisation
  709. Medium-term response of microbial community to rhizodeposits of white clover and ryegrass and tracing of active processes induced by 13C and 15N labelled exudates
  710. Fate of 14C-labeled dissolved organic matter in paddy and upland soils in responding to moisture
  711. Microbial interactions affect sources of priming induced by cellulose
  712. Effect of cactus pear cultivation after Mediterranean maquis on soil carbon stock, δ13C spatial distribution and root turnover
  713. Sorption affects amino acid pathways in soil: Implications from position-specific labeling of alanine
  714. Erratum to “Effect of land-use and elevation on microbial biomass and water extractable carbon in soils of Mt. Kilimanjaro ecosystems” [Appl. Soil Ecol. 67 (2013) 10–19]
  715. Glucose decomposition and its incorporation into soil microbial biomass depending on land use in Mt. Kilimanjaro ecosystems
  716. Soil C and N availability determine the priming effect: microbial N mining and stoichiometric decomposition theories
  717. Microbial Growth and Carbon Use Efficiency in the Rhizosphere and Root-Free Soil
  718. Pathways of litter C by formation of aggregates and SOM density fractions: Implications from 13C natural abundance
  719. Spatial distribution and turnover of root-derived carbon in alfalfa rhizosphere depending on top- and subsoil properties and mycorrhization
  720. Plant traits regulating N capture define microbial competition in the rhizosphere
  721. Biochar stability in soil: Decomposition during eight years and transformation as assessed by compound-specific 14C analysis
  722. Nutrient limitation of alpine plants: Implications from leaf N : P stoichiometry and leaf δ15N
  723. Spatial and temporal dynamics of hotspots of enzyme activity in soil as affected by living and dead roots—a soil zymography analysis
  724. Improved δ13 C analysis of amino sugars in soil by ion chromatography-oxidation-isotope ratio mass spectrometry
  725. Comparison of net ecosystem CO2 exchange in cropland and grassland with an automated closed chamber system
  726. Carbon cost of collective farming collapse in Russia
  727. Effects of 15 years of manure and mineral fertilizers on enzyme activities in particle-size fractions in a North China Plain soil
  728. Mechanisms of rhizosphere priming effects and their ecological significance
  729. Labile carbon retention compensates for CO2released by priming in forest soils
  730. Active microorganisms in soil: Critical review of estimation criteria and approaches
  731. Biochemical pathways of amino acids in soil: Assessment by position-specific labeling and 13C-PLFA analysis
  732. Distribution of microbial- and root-derived phosphatase activities in the rhizosphere depending on P availability and C allocation – Coupling soil zymography with 14C imaging
  733. Microbial gross organic phosphorus mineralization can be stimulated by root exudates – A 33P isotopic dilution study
  734. Microbial response to rhizodeposition depending on water regimes in paddy soils
  735. Biogeochemical transformations of amino acids in soil assessed by position-specific labelling
  736. Silicon uptake by wheat: Effects of Si pools and pH
  737. Turnover and availability of soil organic carbon under different Mediterranean land-uses as estimated by13C natural abundance
  738. Phosphorus mineralization can be driven by microbial need for carbon
  739. Labile soil organic matter fractions as influenced by non-flooded mulching cultivation and cropping season in rice–wheat rotation
  740. Effect of land-use and elevation on microbial biomass and water extractable carbon in soils of Mt. Kilimanjaro ecosystems
  741. Integrated management systems and N fertilization: effect on soil organic matter in rice-rapeseed rotation
  742. Competition between roots and microorganisms for nitrogen: mechanisms and ecological relevance
  743. Effects of polyacrylamide, biopolymer and biochar on the decomposition of14C-labelled maize residues and on their stabilization in soil aggregates
  744. Bicarbonate as tracer for assimilated C and homogeneity of 14C and 15N distribution in plants by alternative labeling approaches
  745. Soil zymography – A novel in situ method for mapping distribution of enzyme activity in soil
  746. Effect of clipping and shading on C allocation and fluxes in soil under ryegrass and alfalfa estimated by 14C labelling
  747. Nutrient acquisition from arable subsoils in temperate climates: A review
  748. Plant inter-species effects on rhizosphere priming of soil organic matter decomposition
  749. Fate of fertilizer 15N in intensive ridge cultivation with plastic mulching under a monsoon climate
  750. C and N allocation in soil under ryegrass and alfalfa estimated by 13C and 15N labelling
  751. Soil organic carbon decomposition from recently added and older sources estimated by δ13C values of CO2 and organic matter
  752. Carbon allocation in grassland communities under drought stress followed by 14C pulse labeling
  753. Soils of an Early Medieval (4th–6th Centuries) Settlement in the Middle Tobol Region and their Paleogeographic Implication
  754. Decomposition of biogas residues in soil and their effects on microbial growth kinetics and enzyme activities
  755. N fluxes in an agricultural catchment under monsoon climate: A budget approach at different scales
  756. Effects of land use intensity on dissolved organic carbon properties and microbial community structure
  757. Estimation of rhizodeposition at field scale: upscaling of a 14C labeling study
  758. Allocation and dynamics of assimilated carbon in rice-soil system depending on water management
  759. Use of molecular ratios to identify changes in fatty acid composition of Miscanthus×giganteus (Greef et Deu.) plant tissue, rhizosphere and root-free soil during a laboratory experiment
  760. Carbon flow into microbial and fungal biomass as a basis for the belowground food web of agroecosystems
  761. Pedogenic carbonate formation: Recrystallization versus migration-Process rates and periods assessed by14C labeling
  762. Soil organic carbon and total nitrogen in intensively managed arable soils
  763. Soil microbial biomass and its activity estimated by kinetic respiration analysis – Statistical guidelines
  764. Effects of polyacrylamide, biopolymer, and biochar on decomposition of soil organic matter and plant residues as determined by 14C and enzyme activities
  765. Erratum to “Carbonate rhizoliths in loess and their implications for paleoenvironmental reconstruction revealed by isotopic composition: δ13C, 14C” [Chemical Geology 283 (2011) 251–260]
  766. Processes of Soil Carbon Dynamics and Ecosystem Carbon Cycling in a Changing World
  767. Effects of 15 years of manure and inorganic fertilizers on soil organic carbon fractions in a wheat-maize system in the North China Plain
  768. Effect of grazing on carbon stocks and assimilate partitioning in a Tibetan montane pasture revealed by 13CO2 pulse labeling
  769. Differentiation of plant derived organic matter in soil, loess and rhizoliths based on n-alkane molecular proxies
  770. Effect of temperature and rhizosphere processes on pedogenic carbonate recrystallization: Relevance for paleoenvironmental applications
  771. Response of long-, medium- and short-term processes of the carbon budget to overgrazing-induced crusts in the Tibetan Plateau
  772. Plant-mediated CH<sub>4</sub> transport and contribution of photosynthates to methanogenesis at a boreal mire: a <sup>14</sup>C pulse-labeling study
  773. Direct phloem transport and pressure concentration waves in linking shoot and rhizosphere activity.
  774. Ecology: Prime time for microbes
  775. Pedogenic carbonate recrystallization assessed by isotopic labeling: a comparison of 13C and 14C tracers
  776. Effects of anionic polyacrylamide on maize growth: a short term 14C labeling study
  777. How to link soil C pools with CO<sub>2</sub> fluxes?
  778. Identification of labile and stable pools of organic matter in an agrogray soil
  779. Drought effects on microbial biomass and enzyme activities in the rhizosphere of grasses depend on plant community composition
  780. Stem labeling results in different patterns of 14C rhizorespiration and 15N distribution in plants compared to natural assimilation pathways
  781. Carbonate rhizoliths in loess and their implications for paleoenvironmental reconstruction revealed by isotopic composition: δ13C, 14C
  782. Three-source-partitioning of microbial biomass and of CO2 efflux from soil to evaluate mechanisms of priming effects
  783. C and N in soil organic matter density fractions under elevated atmospheric CO2: Turnover vs. stabilization
  784. How to link soil C pools with CO2 fluxes?
  785. Photoassimilate allocation and dynamics of hotspots in roots visualized by 14C phosphor imaging
  786. Spatio-temporal variations determine plant-microbe competition for inorganic nitrogen in an alpine meadow
  787. Priming Effects in Relation to Soil Conditions – Mechanisms
  788. Turnover of soil organic matter and of microbial biomass under C3–C4 vegetation change: Consideration of 13C fractionation and preferential substrate utilization
  789. Dominant plant species shift their nitrogen uptake patterns in response to nutrient enrichment caused by a fungal fairy in an alpine meadow
  790. Effects of aggregation processes on distribution of aggregate size fractions and organic C content of a long-term fertilized soil
  791. Rhizoliths in loess – evidence for post-sedimentary incorporation of root-derived organic matter in terrestrial sediments as assessed from molecular proxies
  792. Responses of ecosystem carbon dioxide fluxes to soil moisture fluctuations in a moist Kenyan savanna
  793. Priming effects: Interactions between living and dead organic matter
  794. 13C fractionation at the root–microorganisms–soil interface: A review and outlook for partitioning studies
  795. Fast incorporation of root-derived lipids and fatty acids into soil – Evidence from a short term multiple pulse labelling experiment
  796. Effect of fertilization on decomposition of 14C labelled plant residues and their incorporation into soil aggregates
  797. Model of apparent and real priming effects: Linking microbial activity with soil organic matter decomposition
  798. Microbial uptake of low-molecular-weight organic substances out-competes sorption in soil
  799. Growth rates of rhizosphere microorganisms depend on competitive abilities of plants and N supply
  800. Carbonate recrystallization in root-free soil and rhizosphere of Triticum aestivum and Lolium perenne estimated by 14C labeling
  801. Source determination of lipids in bulk soil and soil density fractions after four years of wheat cropping
  802. Effect of CO2 concentration on the initial recrystallization rate of pedogenic carbonate — Revealed by 14C and 13C labeling
  803. Plant uptake of dual-labeled organic N biased by inorganic C uptake: Results of a triple labeling study
  804. Influence of defoliation on CO2 efflux from soil and microbial activity in a Mediterranean grassland
  805. Elevated atmospheric CO2increases microbial growth rates in soil: results of three CO2enrichment experiments
  806. Rhizodeposition of maize: Short-term carbon budget and composition
  807. Sorption, microbial uptake and decomposition of acetate in soil: Transformations revealed by position-specific 14C labeling
  808. Optimization of 14C liquid scintillation counting of plant and soil lipids to trace short term formation, translocation and degradation of lipids
  809. REVIEW: Time lag between photosynthesis and carbon dioxide efflux from soil: a review of mechanisms and controls
  810. 10.1007/s11475-008-2006-1
  811. Nitrogen uptake and utilisation as a competition factor between invasive Duchesnea indica and native Fragaria vesca
  812. Effects of 11 years of conservation tillage on soil organic matter fractions in wheat monoculture in Loess Plateau of China
  813. Respiration costs associated with nitrate reduction as estimated by 14CO2 pulse labeling of corn at various growth stages
  814. Three-source partitioning of CO2efflux from maize field soil by13C natural abundance
  815. Carbon isotopes as proof for plant uptake of organic nitrogen: Relevance of inorganic carbon uptake
  816. Stimulation of r- vs. K-selected microorganisms by elevated atmospheric CO2 depends on soil aggregate size
  817. Plant lipid composition is not affected by short-term isotopic (13C) pulse-labelling experiments
  818. Stimulation of microbial extracellular enzyme activities by elevated CO2depends on soil aggregate size
  819. Contrasting effects of glucose, living roots and maize straw on microbial growth kinetics and substrate availability in soil
  820. Effect of land use types on decomposition of 14C-labelled maize residue (Zea mays L.)
  821. Black carbon decomposition and incorporation into soil microbial biomass estimated by 14C labeling
  822. Comments on the paper by Kemmitt et al. (2008) ‘Mineralization of native soil organic matter is not regulated by the size, activity or composition of the soil microbial biomass – A new perspective’ [Soil Biology & Biochemistry 40, 61–73]: The biology o...
  823. Improved RP-HPLC and anion-exchange chromatography methods for the determination of amino acids and carbohydrates in soil solutions
  824. The rates of organic matter renewal in gray forest soils and chernozems
  825. Thermal stability of soil organic matter pools and their turnover times calculated by δ13C under elevated CO2and two levels of N fertilisation†
  826. Ammonium versus nitrate nutrition of Zea mays and Lupinus albus: Effect on root-derived CO2 efflux
  827. Mechanisms of real and apparent priming effects and their dependence on soil microbial biomass and community structure: critical review
  828. Effect of heavy metals contamination on root-derived and organic matter-derived CO2 efflux from soil planted with Zea mays
  829. Root uptake of N-containing and N-free low molecular weight organic substances by maize: A 14C/15N tracer study
  830. Microbial utilization and mineralization of [14C]glucose added in six orders of concentration to soil
  831. The third international conference “Emission and Sinks of Greenhouse Gases in Northern Eurasia”
  832. Root-derived carbon in soil respiration and microbial biomass determined by 14C and 13C
  833. Root-derived respiration and non-structural carbon of rice seedlings
  834. Carbon pool and sequestration in former arable Chernozems depending on restoration period
  835. A new rapid micro-method for the molecular-chemical characterization of rhizodeposits by field-ionization mass spectrometry
  836. Soil organic matter mineralization and residue decomposition of spring wheat grown under elevated CO2 atmosphere
  837. Light affects competition for inorganic and organic nitrogen between maize and rhizosphere microorganisms
  838. Carbohydrate and amino acid composition of dissolved organic matter leached from soil
  839. Effects of nitrogen and intensive mixing on decomposition of 14C-labelled maize (Zea mays L.) residue in soils of different land use types
  840. Priming effects in Chernozem induced by glucose and N in relation to microbial growth strategies
  841. Elevation of atmospheric CO2 and N-nutritional status modify nodulation, nodule-carbon supply, and root exudation of Phaseolus vulgaris L.
  842. Carbon sequestration underMiscanthus in sandy and loamy soils estimated by natural13C abundance
  843. Effects of atmospheric CO2 enrichment on δ 13C, δ 15N values and turnover times of soil organic matter pools isolated by thermal techniques
  844. Separation of root and microbial respiration: Comparison of three methods
  845. Thermal stability of soil organic matter pools and their δ13C values after C3–C4 vegetation change
  846. Carbon balance in the soils of abandoned lands in Moscow region
  847. Response of root respiration and root exudation to alterations in root C supply and demand in wheat
  848. Root exudate components change litter decomposition in a simulated rhizosphere depending on temperature
  849. Response to the comments by Peter Högberg, Nina Buchmann and David J. Read on the review ‘Sources of CO2 efflux from soil and review of partitioning methods’ (Soil Biology & Biochemistry 38, 425–448)Object- versus method-oriented terminology
  850. Three-source partitioning of CO2 efflux from soil planted with maize by 13C natural abundance fails due to inactive microbial biomass
  851. Silicon pools and fluxes in soils and landscapes—a review
  852. Carbon fluxes in soil food webs of increasing complexity revealed by 14C labelling and 13C natural abundance
  853. Contribution of rhizomicrobial and root respiration to the CO2 emission from soil (A review)
  854. Assimilate partitioning affects 13C fractionation of recently assimilated carbon in maize
  855. Silicon pools and fluxes in soils and landscapes—a review
  856. Spatial distribution of root exudates of five plant species as assessed by14C labeling
  857. Significance of organic nitrogen acquisition for dominant plant species in an alpine meadow on the Tibet plateau, China
  858. Effect of C3–C4 Vegetation Change on δ13C and δ15N Values of Soil Organic Matter Fractions Separated by Thermal Stability
  859. Glucose uptake by maize roots and its transformation in the rhizosphere
  860. Sources and mechanisms of priming effect induced in two grassland soils amended with slurry and sugar
  861. Remediation of a soil contaminated with heavy metals by immobilizing compounds
  862. Carbonate re-crystallization in soil revealed by 14C labeling: Experiment, model and significance for paleo-environmental reconstructions
  863. Sources of CO2 efflux from soil and review of partitioning methods
  864. Below-ground partitioning (14C) and isotopic fractionation (δ13C) of carbon recently assimilated by maize
  865. Root and rhizomicrobial respiration: A review of approaches to estimate respiration by autotrophic and heterotrophic organisms in soil
  866. Effect of Immobilizing Substances and Salinity on Heavy Metals Availability to Wheat Grown on Sewage Sludge-Contaminated Soil
  867. Comparative efficacy of ZnSO4 and Zn-EDTA application for fertilization of rice (Oryza sativaL.)
  868. Effect of Clay Minerals on Immobilization of Heavy Metals and Microbial Activity in a Sewage Sludge-Contaminated Soil (8 pp)
  869. Three sources of CO2 efflux from soil partitioned by13C natural abundance in an incubation study
  870. Theoretical background for partitioning of root and rhizomicrobial respiration by δ13C of microbial biomass
  871. Using natural13C abundances to differentiate between three CO2 sources during incubation of a grassland soil amended with slurry and sugar
  872. Dynamics of Organic C Mineralization and the Mobile Fraction of Heavy Metals in a Calcareous Soil Incubated with Organic Wastes
  873. Plant and mycorrhizal regulation of rhizodeposition
  874. Photosynthesis controls of CO2efflux from maize rhizosphere
  875. Effect of clay minerals on extractability of heavy metals and sewage sludge mineralization in soil
  876. Einfluss von Tonmineralen und Fe-Oxiden auf die Mobilität von Schwermetallen und deren Aufnahme durch Weizen
  877. Abschätzung des Beitrages von Miscanthus zur Bildung der organischen Bodensubstanz mit Hilfe der natürlichen 13C-Abundanz
  878. Qualitative assessment of rhizodeposits in non-sterile soil by analytical pyrolysis
  879. Quantification of priming and CO2 respiration sources following slurry-C incorporation into two grassland soils with different C content
  880. Photosynthesis as a factor controlling short-term C turnover in the rhizosphere
  881. Einfluss des Pflanzenwachstums und der organischen Substanz auf C- und N- Umsatz im Boden
  882. Separating microbial respiration of exudates from root respiration in non-sterile soils: a comparison of four methods
  883. Carbon partitioning in plant and soil, carbon dioxide fluxes and enzyme activities as affected by cutting ryegrass
  884. Effect of nitrogen fertilisation on below-ground carbon allocation in lettuce
  885. Photosynthesis controls of rhizosphere respiration and organic matter decomposition
  886. Carbon partitioning and below-ground translocation by Lolium perenne
  887. Review of mechanisms and quantification of priming effects
  888. Carbon input by plants into the soil. Review
  889. Measurement of the carbon fluxes in the rhizosphere of Lolium perenne
  890. Decrease of humus decomposition during growth of Lolium perenne — negative priming effect
  891. Oxidation of methane and dehydrogenase activity in a Mollic Gleysol
  892. The role of amino acids and nucleic bases in turnover of nitrogen and carbon in soil humic fractions
  893. Wirkung des Mikroreliefs auf die räumliche Variabilität des Kohlenstoffgehaltes eines Podzoluvisols in einem Dauerdüngungsversuch
  894. Zeitreihenanalyse der Temperaturdynamik eines Sandbodens
  895. MODELLING ON THE GROWTH AND N UPTAKE OF LEEK AND BROCCOLI
  896. NITROGEN UPTAKE AND NITROGEN LOSSES IN FIELD TRIALS WITH CARROTS