Small but active – pool size does not matter for carbon incorporation in below‐ground food webs

No abstract is available for this paper.

• Publication year

  2016

• Venue

  Functional Ecology

• Publication date

  2016-03-01

• Fields of study

  Biology, Environmental Science

• Identifiers
  DOI 10.1111/1365-2435.12512
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Partitioning NEE for absolute C input into various ecosystem pools by combining results from eddy-covariance, atmospheric flux partitioning and 13CO2 pulse labeling

  2015cited by this paper
• Free‐living nematodes as prey for higher trophic levels of forest soil food webs

  2014cited by this paper
• Collembola grazing on arbuscular mycorrhiza fungi modulates nutrient allocation in plants

  2014cited by this paper
• Combined ¹³C and ¹⁵N isotope analysis on small samples using a near-conventional elemental analyzer/isotope ratio mass spectrometer setup.

  2014cited by this paper
• Selective transport of plant root-associated bacterial populations in agricultural soils upon snowmelt

  2014cited by this paper
• Linking microbial community structure and allocation of plant-derived carbon in an organic agricultural soil using 13CO2 pulse-chase labelling combined with 13C-PLFA profiling

  2013cited by this paper
• Divergence of feeding channels within the soil food web determined by ecosystem type

  2013cited by this paper
• Estimation of rhizodeposition at field scale: upscaling of a 14C labeling study

  2013cited by this paper
• Large 13C/12C and small 15N/14N isotope fractionation in an experimental detrital foodweb (litter–fungi–collembolans)

  2013cited by this paper
• Empirically Characterising Trophic Networks: What Emerging DNA-Based Methods, Stable Isotope and Fatty Acid Analyses Can Offer

  2013cited by this paper
• Temporal variation in surface and subsoil abundance and function of the soil microbial community in an arable soil

  2013cited by this paper
• Soil organic carbon decomposition from recently added and older sources estimated by δ13C values of CO2 and organic matter

  2012cited by this paper
• Carbon flow into microbial and fungal biomass as a basis for the belowground food web of agroecosystems

  2012cited by this paper
• Protozoan Pulses Unveil Their Pivotal Position Within the Soil Food Web

  2011cited by this paper
• Isotopic signature (15N/14N and 13C/12C) confirms similarity of trophic niches of millipedes (Myriapoda, diplopoda) in a temperate deciduous forest

  2011cited by this paper
• Rapid transfer of photosynthetic carbon through the plant-soil system in differently managed species-rich grasslands

  2011cited by this paper
• Soil‐carbon turnover under different crop management: Evaluation of RothC‐model predictions under Pannonian climate conditions

  2010cited by this paper
• Contribution of nematodes to the structure and function of the soil food web.

  2010cited by this paper
• Shifting carbon flow from roots into associated microbial communities in response to elevated atmospheric CO2

  2010influential reference
• The fat that matters: Soil food web analysis using fatty acids and their carbon stable isotope signature

  2010cited by this paper
• Negligible contribution from roots to soil-borne phospholipid fatty acid fungal biomarkers 18:2ω6,9 and 18:1ω9

  2010cited by this paper
• Three-source partitioning of CO2 efflux from maize field soil by 13C natural abundance

  2009cited by this paper
• Collembola switch diet in presence of plant roots thereby functioning as herbivores.

  2009cited by this paper
• Dissipation of bacterially derived C and N through the meso- and macrofauna of a grassland soil

  2009cited by this paper
• Microbial community composition and rhizodeposit-carbon assimilation in differently managed temperate grassland soils

  2009cited by this paper
• Climate change 2007. Synthesis report. Contribution of Working Groups I, II and III to the fourth assessment report

  2008cited by this paper
• From peds to paradoxes: linkages between soil biota and their influences on ecological processes.

  2008cited by this paper
• Carbon routes from decomposing plant residues and living roots into soil food webs assessed with 13C labelling

  2008cited by this paper
• Combining Results of Two GC Separations Partly Achieves Determination of All cis and trans 16:1, 18:1, 18:2 and 18:3 Except CLA Isomers of Milk Fat as Demonstrated Using Ag-Ion SPE Fractionation

  2008cited by this paper
• Dynamics of litter carbon turnover and microbial abundance in a rye detritusphere

  2008cited by this paper
• Isotopic detection of recent photosynthate carbon flow into grassland rhizosphere fauna

  2007cited by this paper
• Stable isotopes of carbon and nitrogen in soil ecological studies

  2007cited by this paper
• The underestimated importance of belowground carbon input for forest soil animal food webs.

  2007cited by this paper
• Soil organic matter dynamics in grassland soils under elevated CO2: Insights from long-term incubations and stable isotopes

  2007cited by this paper
• Maize Root Biomass and Net Rhizodeposited Carbon

  2006cited by this paper
• Carbon fluxes from plants through soil organisms determined by field 13CO2 pulse-labelling in an upland grassland

  2006cited by this paper
• Incorporation of plant carbon into the soil animal food web of an arable system.

  2006cited by this paper
• Carbon fluxes in soil food webs of increasing complexity revealed by 14C labelling and 13C natural abundance

  2006cited by this paper
• Interactions Between Microorganisms and Soil Micro- and Mesofauna

  2005cited by this paper
• Modeling trophic pathways, nutrient cycling, and dynamic stability in soils

  2005cited by this paper
• Protozoa and plant growth: the microbial loop in soil revisited.

  2004cited by this paper
• Ecological Linkages Between Aboveground and Belowground Biota

  2004cited by this paper
• Identification of groups of metabolically-active rhizosphere microorganisms by stable isotope probing of PLFAs

  2004cited by this paper
• Estimation of conversion factors for fungal biomass determination in compost using ergosterol and PLFA 18 : 2 omega 6,9

  2004cited by this paper
• Decomposition pathways and successional changes

  2004cited by this paper
• Microbial Community Dynamics Associated with Rhizosphere Carbon Flow

  2003influential reference
• Calculating isotopic fractionation from atmospheric measurements at various scales

  2003cited by this paper
• Short communication Reciprocal transfer of carbon and nitrogen by decomposer fungi at the soil -litter interface

  2003cited by this paper
• Fatty acids of fungi and nematodes—possible biomarkers in the soil food chain?

  2002cited by this paper
• The soil food web of two beech forests (Fagus sylvatica) of contrasting humus type: stable isotope analysis of a macro- and a mesofauna-dominated community

  2000cited by this paper
• Food preferences of a fungal-feeding Aphelenchoides species.

  2000cited by this paper
• Long-term manipulation of the microbes and microfauna of two subarctic heaths by addition of fungicide, bactericide, carbon and fertilizer

  2000cited by this paper
• Nematode diversity in agroecosystems

  1999cited by this paper
• Continuous flow isotope ratio mass spectrometry of carbon dioxide trapped as strontium carbonate

  1997cited by this paper
• Nematode Fauna in Spruce Forest Soils: a Qualitative/ Quantitative Comparison

  1995cited by this paper
• Energetics, Patterns of Interaction Strengths, and Stability in Real Ecosystems

  1995cited by this paper
• Microbial-feeding nematodes and protozoa in soil: Their effectson microbial activity and nitrogen mineralization in decomposition hotspots and the rhizosphere

  1994cited by this paper
• Calculation of nitrogen mineralization in soil food webs

  1993cited by this paper
• The exploitation of food resources by soil meso- and macro invertebrates

  1993cited by this paper
• Microbial biomass measured as total lipid phosphate in soils of different organic content

  1991cited by this paper
• Measurement of soil microbial biomass C by fumigation-extraction—an automated procedure

  1990cited by this paper
• AN EXTRACTION METHOD FOR MEASURING SOIL MICROBIAL BIOMASS C

  1987cited by this paper
• A new extractor for woodland litter

  1963cited by this paper
• Microbial-feeding nematodes and protozoa in soil : Their effects on microbial activity and nitrogen mineralization in decomposition hotspots and the rhizosphere

  year unknowncited by this paper

• Long term low-level nitrogen addition enhances microbial carbon use efficiency and turnover rate across different seasons

  2026cites this paper
• A soil food web approach to integrate soil fauna into multitrophic biogeochemistry

  2026cites this paper
• Relay strip intercropping boosts fungal and bacterial contributions to soil organic carbon

  2026cites this paper
• Effects of fertilization regimes on active microbial groups in photosynthetic carbon utilization

  2025cites this paper
• Stover return enhances the transformation and sequestration of photosynthetic carbon through regulating soil food web

  2025cites this paper
• Phosphorus-transforming microbes enhance phosphatase catalytic efficiency to alleviate phosphorus limitation under nitrogen and phosphorus additions in subtropical forest soil

  2025cites this paper
• Tracking assimilation of microbial biomass, leaf litter and artificially created soil organic matter by soil fauna using multi-resource stable isotope labelling

  2025cites this paper
• Organic substrate quality influences microbial community assembly and nitrogen transport to plants in the hyphosphere of a temperate grassland soil

  2025cites this paper
• Cascading Effects Within Soil Food Web Amplify Fungal Biomass and Necromass Production

  2025cites this paper
• Quantitative stable isotope probing (qSIP) and cross-domain networks reveal bacterial-fungal interactions in the hyphosphere

  2025cites this paper
• Impact of Erosion-Induced Topsoil Dilution on Rapeseed Root Growth, Assimilate C Input, and Turnover in the Soil

  2025cites this paper
• Stability of soil structure in response to cations‐carbon‐microbial linkages with manure application in the coastal saline‐alkaline soil, China

  2025influential citation
• JenaTron - An Experimental Approach to Study the Effects of Plant History and Soil History on Grassland Ecosystem Functioning.

  2025cites this paper
• A Model of the Ectomycorrhizal Contribution to Forest Soil C and N Dynamics and Tree N Supply Within the EFIMOD3 Model System

  2025cites this paper
• High litter quality enhances plant energy channeling by soil macro‐detritivores and lowers their trophic position

  2025cites this paper
• Why oaks should stay with their close relatives: growing in a distantly related neighbourhood delays and reorganizes nutrient recycling during litter decomposition

  2025cites this paper
• Hidden Role of Trophic Cascade Effects for Soil Carbon Sequestration in Alpine Tundra

  2025influential citation
• Linking nematodes and ecosystem function: a trait-based framework.

  2024cites this paper
• Litter quality controls the contribution of microbial carbon to main microbial groups and soil organic carbon during its decomposition

  2024cites this paper
• Cropping systems and ecological groups of soil animals jointly affect the transfer of root-derived carbon and mineral nitrogen into the soil food web

  2024cites this paper
• Mechanism of microbial necromass formation during decomposition of Stipa bungeana above-ground residues

  2024cites this paper
• Addition of microbes shifts the ability of soil carbon sequestration in the process of soil Cd remediation

  2024cites this paper
• Simulated soil erosion predominantly affects fungal abundance in the rapeseed rhizosphere

  2024cites this paper
• Ectomycorrhizal fungi alter soil food webs and the functional potential of bacterial communities

  2024cites this paper
• Regulation of soil organic carbon dynamics by microbial communities during reforestation of Chinese fir plantations after clear‐cutting

  2024cites this paper
• Early changes in carbon uptake and partitioning moderate belowground carbon storage in a perennial grain

  2024cites this paper
• Towards establishing a fungal economics spectrum in soil saprobic fungi

  2024cites this paper
• Phage Mediated Biocontrol: A Promising Green Solution for Sustainable Agriculture

  2024cites this paper
• Afforestation inhibited soil microbial activities along the riparian zone of the upper Yangtze River of China

  2023cites this paper
• Effects of management intensity, soil properties and region on the nematode communities in temperate forests in Germany

  2023cites this paper
• Leguminous crop restores the carbon flow attenuation from nitrogen loading within soil nematode food web in a Camellia oleifera plantation.

  2023cites this paper
• Adaptability of agricultural soil microbial nutrient utilization regulates community assembly under mulching measures on the Loess Plateau

  2023cites this paper
• Bottom-up effects of nematode prey on soil predatory mites (Acari: Mesostigmata)

  2023cites this paper
• Interspecific interactions between crops influence soil functional groups and networks in a maize/soybean intercropping system

  2023cites this paper
• Long-term warming-induced trophic downgrading in the soil microbial food web

  2023cites this paper
• Exogenous carbon turnover within the soil food web strengthens soil carbon sequestration through microbial necromass accumulation

  2023cites this paper
• Bedrock and climate jointly control microbial necromass along a subtropical elevational gradient

  2023cites this paper
• Intensive management disrupts belowground multi-trophic resources transfers in response to drought

  2022cites this paper
• Intensive grassland management disrupts below-ground multi-trophic resource transfer in response to drought

  2022cites this paper
• Microbial utilization of photosynthesized carbon depends on land-use

  2022cites this paper
• The fungal feeding channel of the soil micro‐food web contributes to the transformation of exogenous C into soil C—A 13C labelling microcosm experiment

  2022cites this paper
• The use of stable carbon isotopes to decipher global change effects on soil organic carbon: present status, limitations, and future prospects

  2022cites this paper
• Carbon fluxes within tree-crop-grass agroforestry system: 13C field labeling and tracing

  2022cites this paper
• Effects of irrigation and fertilization practice on soil nematode communities in arable land

  2022cites this paper
• Contribution of rhizodeposit associated microbial groups to SOC varies with maize growth stages

  2022cites this paper
• Flux of Root-Derived Carbon into the Nematode Micro-Food Web: A Comparison of Grassland and Agroforest

  2022cites this paper
• Amino Acid Isotopes in Functional Assemblages of Collembola Reveal the Influence of Vertical Resource Heterogeneity and Root Energy Supply on Trophic Interactions in Soil Food Webs

  2022cites this paper
• High additions of nitrogen affect plant species-specific differences in the composition of main microbial groups and the uptake of rhizodeposited carbon in a grassland soil

  2022cites this paper
• BSSD 2021 Performance Metric Q4

  2021cites this paper
• Nutrient limitation may induce microbial mining for resources from persistent soil organic matter.

  2021cites this paper
• Evaluation of Phenolic Root Exudates as Stimulants of Saptrophic Fungi in the Rhizosphere

  2021cites this paper
• How soil biota regulate C cycling and soil C pools in diversified crop rotations

  2021cites this paper
• Long-term vegetation restoration promotes the stability of the soil micro-food web in the Loess Plateau in North-west China

  2021cites this paper
• Root-o-Mat: A novel tool for 2D image processing of root-soil interactions and its application in soil zymography

  2021cites this paper
• The mineralosphere—interactive zone of microbial colonization and carbon use in grassland soils

  2021cites this paper
• Stable isotopes of amino acids indicate that soil decomposer microarthropods predominantly feed on saprotrophic fungi

  2021cites this paper
• Temporal patterns of carbon flow from grassland vegetation to soil microorganisms measured using 13C-labelling and signature fatty acids

  2021cites this paper
• Stimulated saprotrophic fungi in arable soil extend their activity to the rhizosphere and root microbiomes of crop seedlings

  2021influential citation
• The flux of root-derived carbon via fungi and bacteria into soil microarthropods (Collembola) differs markedly between cropping systems

  2021cites this paper
• Community RNA-Seq: multi-kingdom responses to living versus decaying roots in soil

  2021cites this paper
• Mass Spectrometry Imaging: NanoSIMS-based approaches

  2021cites this paper
• Effects of resource manipulation on nematode community structure and metabolic footprints in an arable soil across time and depth

  2020cites this paper
• Incorporation of root-derived carbon into soil microarthropods varies between cropping systems

  2020cites this paper
• Identification of fungal populations assimilating rice root residue-derived carbon by DNA stable-isotope probing

  2020cites this paper
• Root herbivory controls the effects of water availability on the partitioning between above‐ and below‐ground grass biomass

  2020cites this paper
• Responses of soil nitrogen and phosphorus cycling to drying and rewetting cycles: A meta-analysis

  2020cites this paper
• Rhizosphere control of soil nitrogen cycling: a key component of plant economic strategies

  2020cites this paper
• KEYLINK: towards a more integrative soil representation for inclusion in ecosystem scale models. I. review and model concept

  2020cites this paper
• Diesel Impacts on Functional Bacterial Groups and Collembolans During Phytoremediation in a Mesocosm System

  2020cites this paper
• The physical structure of soil: Determinant and consequence of trophic interactions

  2020cites this paper
• The microbial community size, structure, and process rates along natural gradients of soil salinity

  2019cites this paper
• Trophic and non-trophic interactions in binary links affect carbon flow in the soil micro-food web

  2019cites this paper
• Drought decreases incorporation of recent plant photosynthate into soil food webs regardless of their trophic complexity

  2019cites this paper
• Microbial growth and carbon use efficiency in soil: Links to fungal-bacterial dominance, SOC-quality and stoichiometry

  2019cites this paper
• Additions of sugar and nitrogenous fertiliser affect plant nitrogen status and soil microbial communities

  2019cites this paper
• Reforestation accelerates soil organic carbon accumulation: Evidence from microbial biomarkers

  2019cites this paper
• Diversity and specificity of lipid patterns in basal soil food web resources

  2019cites this paper
• Effects of long-term tillage on carbon partitioning of nematode metabolism in a Black soil of Northeast China

  2019cites this paper
• Disentangling carbon flow across microbial kingdoms in the rhizosphere of maize

  2019cites this paper
• Impacts of Browsing and Grazing Ungulates on Soil Biota and Nutrient Dynamics

  2019cites this paper
• Essential Biomolecules in Food Webs

  2019cites this paper
• Long-term fertilization management affects the C utilization from crop residues by the soil micro-food web

  2018cites this paper
• Carbon input by roots into the soil: Quantification of rhizodeposition from root to ecosystem scale

  2018cites this paper
• In the land of plenty: catch crops trigger nitrogen uptake by soil microorganisms

  2018cites this paper
• Advances and Perspectives in Soil Nematode Ecology in China

  2018cites this paper
• Long-term fertilization management affects the C utilization from crop residues by the soil micro-food web

  2018cites this paper
• Insights into fungal communities colonizing the acarosphere in a forest soil habitat

  2018cites this paper
• Using plant, microbe, and soil fauna traits to improve the predictive power of biogeochemical models

  2018cites this paper
• Modulation of Litter Decomposition by the Soil Microbial Food Web Under Influence of Land Use Change

  2018cites this paper
• Viruses in soil: Nano-scale undead drivers of microbial life, biogeochemical turnover and ecosystem functions

  2018cites this paper
• Carbon budgets of top- and subsoil food webs in an arable system

  2018cites this paper
• Nematodes as Important Source for Omega-3 Long-Chain Fatty Acids in the Soil Food Web and the Impact in Nutrition for Higher Trophic Levels

  2018cites this paper
• Insights into fungal communities colonizing the acarosphere in a forest soil habitat

  2018cites this paper
• Crop Rotation and Straw Application Impact Microbial Communities in Italian and Philippine Soils and the Rhizosphere of Zea mays

  2018cites this paper
• Grazing and resource availability control soil nematode body size and abundance–mass relationship in semi‐arid grassland

  2018cites this paper
• Below‐ground connections underlying above‐ground food production: a framework for optimising ecological connections in the rhizosphere

  2017cites this paper
• Micropredator niche differentiation between bulk soil and rhizosphere of an agricultural soil depends on bacterial prey

  2017cites this paper
• The tree species matters: Belowground carbon input and utilization in the myco-rhizosphere

  2017cites this paper
• Soil salinity as a driver of microbial community structure and functioning

  2017cites this paper
• Soil carbon loss regulated by drought intensity and available substrate: A meta-analysis

  2017cites this paper