All Stories

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