Microbial community composition and rhizodeposit-carbon assimilation in differently managed temperate grassland soils
By K. Denef, D. Roobroeck, Mihiri C.W. Manimel Wadu, P. Lootens, P. Boeckx. 2009
242 citations recorded by the source corpus.
Subfields: Ecology, Soil Science
View Paper: https://www.semanticscholar.org/paper/b2a73f5906e4dfe019a7d04f7a0cd2095150527b
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In Ecology
In Soil Science
- Y. Kuzyakov
- E. Blagodatskaya
- J. Pausch
- M. Bonkowski
- R. Bardgett
- S. Scheu
- Jordi Sardans
- Josep Peñuelas
Citations in the corpus
- Seasonal controls on grassland microbial biogeography: Are they governed by plants, abiotic properties or both? (2014, background): “The fungal PLFA associated with saprotrophic fungi often increases after mowing in response to increased C input to the soil from exudation, and fungi can also take advantage of the recalcitrant carbon in litter (Bardgett et al., 1996; Denef et al., 2009).”
- Factors affecting soil microbial community structure in tomato cropping systems (2010, background): “In grassland soils, Gram-positive bacteria and actinomycetes were less involved in processing of rhizodeposits than other microbial groups (Denef et al., 2009).”
- Contribution of exudates, arbuscular mycorrhizal fungi and litter depositions to the rhizosphere priming effect induced by grassland species (2015, background): “The deposition of exudates is closely connected to the plant photosynthetic activity, with a transfer of photosynthates to rhizosphere microorganisms occurring in less than 24 hours (Johnson et al., 2002; Denef et al., 2009; De Deyn et al., 2011).”
- Small but active – pool size does not matter for carbon incorporation in below‐ground food webs (2016, background): “High incorporation of root-derived C into Gram-negative PLFA markers 16:1x7 and 18:1x7 has been reported earlier (Treonis et al. 2004; Denef et al. 2009; Tavi et al. 2013).”
- Rapid transfer of photosynthetic carbon through the plant-soil system in differently managed species-rich grasslands (2011, background): “In the aforementioned studies of Bradley et al. (2006) and Denef et al. (2009) the levels of N applications that did cause significant shifts in soil PLFA abundances, irrespective of time since application, and their signature of new photosynthate-C were much higher: ranging from 225 to 450 kg…”
- Microbial response to rhizodeposition depending on water regimes in paddy soils (2013, background): “A number of studies have documented that rhizosphere microbial communities are strongly influenced by rhizo-C (e.g. Butler et al., 2003; Treonis et al., 2004; Paterson et al., 2007; Denef et al., 2009; Jin and Evans, 2010).”
- Active microorganisms in soil: Critical review of estimation criteria and approaches (2013, background): “Phospholipid fatty acids (PLFA) are found only in living cells and thus are characteristic biomarkers for living microorganisms (Zelles,1999; Kramer and Gleixner, 2006; Denef et al., 2009).”
- Connecting the green and brown worlds . allometric and stoichiometric predictability of above- and below-ground networks (2013, background): “…carbohydrates, allocated to different plant tissues and transferred to the soil via root respiration, exudation, mycorrhizae, endophytes and herbivory (Bahn et al., 2010, 2013; Brüggemann et al., 2011; Denef et al., 2009; Epron et al., 2012; Jones et al., 2009; Ostle et al., 2007).”
- Water Conservation and Plant Survival Strategies of Rhizobacteria under Drought Stress (2020, background): “Plants have an antioxidant defensive system which prevents cellular membranes and DNA from ROS-induced oxidative damage by converting ROS into non-toxic forms such as water and oxygen [18,19].”