Soil microbial community patterns related to the history and intensity of grazing in sub montane ecosystems.

By R. Bardgett, A. C. Jones, David L. Jones, S. Kemmitt, R. Cook, P. Hobbs. 2001

253 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/3e87cdfdfa4b86186dd8506cdb341cbdf63c85d5

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In Ecology

In Soil Science

Citations in the corpus

Do herbivores cause habitat degradation or vegetation state transition? Evidence from the tundra (2006, background): “Under such a vegetation state, increased decomposer activity in the soil enhances soil nutrient availability, thereby allowing plant productivity to be maintained at an elevated level (Bardgett et al. 2001, Olofsson et al. 2001, Bardgett and Wardle 2003 ).”
Grazing history effects on above- and below-ground litter decomposition and nutrient cycling in two co-occurring grasses (2008, background): “…grazers have been found to enhance soil nitrogen availability and litter breakdown (Shariff et al. 1994; McNaughton et al. 1997; Tracy and Frank 1998; Olofsson and Oksanen 2002), with concomitant shifts in functional composition of the soil biota (Bardgett et al. 2001; Grayston et al. 2004).”
Plant species diversity, plant biomass and responses of the soil community on abandoned land across Europe: idiosyncracy or above-belowground time lags (2003, background): “Different management regimes of grasslands are known to alter the biomass of soil fauna and to change the composition of microbial communities (Bardgett et al. 1996, 2001, Bardgett and Cook 1998, Donnison et al. 2000, Hedlund 2002).”
Linking aboveground and belowground communities: the indirect influence of aphid species identity and diversity on a three trophic level soil food web (2004, unknown): “(Bardgett et al. 2001), induction of secondary defense”
Nematodes as soil indicators: functional and biodiversity aspects (2003, background): “Bardgett et al. (2001) have provided evidence that soil microbial communities of heavily grazed sites are dominated by bacterial-based energy channels of decomposition, whereas in systems that are less intensively grazed, or completely unmanaged, fungi have a proportionally greater role.”
Tree physiological responses to above-ground herbivory directly modify below-ground processes of soil carbon and nitrogen cycling (2004, background): “Ruess & McNaughton 1987; McNaughton et al. 1997; Frank & Groffman 1998; Tracy & Frank 1998; Stark et al. 2000; Bardgett et al. 2001; Wardle et al. 2001) or negative (e.g.”
LARGE HERBIVORES SUPPRESS DECOMPOSER ABUNDANCE IN A SEMIARID GRAZING ECOSYSTEM (2004, background): “…response to grazing in this study suggests that grazer-induced changes in C inputs to soils may have been accompanied by corresponding shifts in microbial community composition toward species that allocated more carbon to maintenance requirements than to biosynthesis (Bardgett et al. 1998, 2001).”
Dietary evenness, prey choice, and human–environment interactions (2004, unknown): “Evenness has also been used by some conservation biologists to consider the effect of human behavior on species diversity [1,12,13,32,39].”
Plant clipping decelerates the mineralization of recalcitrant soil organic matter under multiple grassland species (2012, background): “Moreover, clipping increased the abundance of gram positive bacteria in agreement with other studies (Bardgett et al., 2001; Klumpp et al., 2009).”
Do plant species with different growth strategies vary in their ability to compete with soil microbes for chemical forms of nitrogen (2008, background): “…monocultures of five co-existing grassland species, namely the grasses Agrostis capillaris, Anthoxanthum odoratum, Nardus stricta, Deschampsia flexuosa and the herb Rumex acetosella, were grown in field soil from an acid, unfertilised and semi-natural temperate grassland (Bardgett et al., 2001).”