1992
DOI: 10.1007/bf00317793
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The effect of nitrate-nitrogen supply on bacteria and bacterial-feeding fauna in the rhizosphere of different grass species

Abstract: Microbial growth in the rhizosphere is affected by the release of organic material from roots, so differences in carbon budgets between plants may affect their rhizosphere biology. This was tested by sampling populations of bacteria and bacteriophagous fauna from the rhizosphere of Lolium perenne, Festuca arundinacea, Poa annua, and Poa pratensis, under conditions of high and low nitrate availability. Concentrations of soluble phenolics and lignin varied considerably between the species but were not related to… Show more

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Cited by 73 publications
(31 citation statements)
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“…The stimulation of bacterial feeding nematodes rather than Protozoa in N treatments 1 week before ear emergence corresponds to earlier findings in barley rhizosphere soil (Griffiths 1990;Griffiths et al 1992). However, Protozoa, but not bacterial feeding nematodes were stimulated in NP treatments at this stage.…”
Section: Discussionsupporting
confidence: 64%
See 1 more Smart Citation
“…The stimulation of bacterial feeding nematodes rather than Protozoa in N treatments 1 week before ear emergence corresponds to earlier findings in barley rhizosphere soil (Griffiths 1990;Griffiths et al 1992). However, Protozoa, but not bacterial feeding nematodes were stimulated in NP treatments at this stage.…”
Section: Discussionsupporting
confidence: 64%
“…14 C labelling has shown increased relative allocation of photoassimilated C to soil and higher microbial growth in the rhizosphere in response to high compared to low soil N status (Merckx et al 1987;Liljeroth et al 1990), and Griffiths et al (1992) found a stimulation of rhizosphere nematodes in Namended treatments. Contrary to these findings, a higher relative C allocation belowground was found at low soil N (Johansson 1992) or P (Saggar et al 1997).…”
Section: Introductionmentioning
confidence: 97%
“…Extrinsic factors such as nutrient availability (Bosatta and Berendse, 1984;De Angelis, 1992;Moore et al, 1993), pH (Wardle, 1998) and the amount of detritus in a system (De Angelis et al, 1989) may also drive resistance and resilience. In soil systems, many of these potential driving factors can be altered by plant community composition, including the composition and structure of the soil microbial community (Griffiths et al, 1992;Wardle and Nicholson, 1996), and the chemical properties of the soil (Gastine et al, 2003;Hooper and Vitousek, 1998;Tilman and Wedin, 1991). It is therefore reasonable to predict that the presence of different plant species may result in soil communities with different abilities to resist and recover from disturbances.…”
Section: Introductionmentioning
confidence: 98%
“…Microbial biomass has been shown to correlate with aboveground primary production (Wardle 1992;Zak et al 1994;Wardle and Barker 1997), and to be responsive to those aboveground trophic interactions, such as herbivory, that aect root exudation (reviewed by Bardgett et al 1998). Since soil microbes are consumed by microbivorous animals, changes in microbial biomass and production can be re¯ected in the biomasses of upper trophic groups of soil food webs (Sohlenius 1990;Christensen et al 1992;Griths et al 1992;Parmelee et al 1993;Griths 1994). Mikola and SetaÈ laÈ (1998b) found that in simple heterotrophic food webs containing microbes and nematodes, increased microbial production led to increases in the biomass of microbes and microbivores, and to a marginal increase in the biomass of top predators (i.e., consumers of microbivores).…”
Section: Introductionmentioning
confidence: 98%