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Rhizosphere and root-infecting fungi and the design of ecological field experiments

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Abstract

As part of a wider study into the role of soil fungi in the ecology of the winter annual grass, Vulpia ciliata ssp. ambigua (Le Gall) Stace & Auquier, we applied the fungicides benomyl and prochloraz to three natural populations of the grass growing in East anglia, United Kingdom. The rhizosphere and rootinfecting fungi associated with the three populations were analysed each month between February and May 1992 when plants set seed. There were marked differences between the fungal floras associated with each of the three populations of V. ciliata, despite the fact that associated plant species and soil nutrient status were broadly similar between sites. This was attributed to wide differences in soil pH between the three populations. Prochloraz did not affect fungal abundance, but benomyl decreased the isolation frequencies of Fusarium oxysporum from roots and the frequencies of Penicillium and Trichoderma spp. isolated from rhizosphere soil, and increased the frequency of isolation of Mucor hiemalis from the rhizosphere of V. ciliata. There were also significant increases in the isolation frequencies of F. oxysporum from roots and M. hiemalis, Trichoderma spp. and Phoma fimeti from the rhizosphere of V. ciliata as plants matured. The significance of these results for the design of ecological field experiments are discussed in light of a previous study which has shown that asymptomatic root-infecting fungi can affect plant fecundity and hence abundance in natural populations of V. ciliata. We propose that differences in microbial communities between sites, controlled in part by soil chemistry, are a major factor determining plant performance under field conditions.

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References

  • Brown JC (1958) Soil fungi of some British sand dunes in relation to soil type and succession. J Ecol 46: 641–664

    Google Scholar 

  • Burdon JJ (1987) Diseases and plant population biology. Cambridge University Press, Cambridge

    Google Scholar 

  • Clay K (1988) Fungal endophytes of grasses: a defensive mutualism between plants and fungi. Ecology 69: 10–16

    Google Scholar 

  • Cotton R, Stace CA (1976) Taxonomy of the genus Vulpia (Gramineae). I. Chromosome numbers and geographical distribution of the old world species. Genetica 46: 235–255

    Google Scholar 

  • Edgington LV, Khew KL, Barron GL (1971) Fungitoxic spectrum of benzimidazole compounds. Phytopathology 61: 42–44

    Google Scholar 

  • Gauch HG (1982) Multivariate analysis in community ecology. Cambridge University Press, Cambridge

    Google Scholar 

  • Hall G (1986) A species of Rhizoctonia with uninucleate hyphae isolated from the roots of winter wheat. Trans Br Mycol Soc 87: 466–471

    Google Scholar 

  • Harley JL, Waid JS (1955) A method of studying active mycelia on living roots and other surfaces in the soil. Trans Br Mycol Soc 38: 104–118

    Google Scholar 

  • Jensen HL (1931) The fungus flora of the soil. Soil Sci 31: 123–158

    Google Scholar 

  • Kloepper JW, Bowen KL (1991) Quantification of the geocarposphere and rhizosphere effect of peanut (Arachis hypogaea L.). Plant Soil 136: 103–109

    Google Scholar 

  • Mack RN, Pyke DA (1984) The demography of Bromus tectorum: the role of microclimate, grazing and disease. J Ecol 72: 731–748

    Google Scholar 

  • Nan ZB, Long PG, Skipp RA (1992) Use of prochloraz and benomyl drenches to assess the effects of fungal root pathogens on growth of red clover under field conditions. Aust Plant Path 21: 98–103

    Google Scholar 

  • Newsham KK (1994) First record of intracellular sporulation by a coelomycete fungus. Mycol Res 98: 1390–1392

    Google Scholar 

  • Newsham KK, Fitter AH, Watkinson AR (1994) Root pathogenic and arbuscular mycorrhizal fungi determine fecundity of asymptomatic plants in the field. J Ecol 82: 805–814

    Google Scholar 

  • Parkinson D, Thomas A (1969) Studies on fungi in the root region. VIII. Qualitative studies on fungi in the rhizosphere of dawarf bean plants. Plant Soil 31: 299–310

    Google Scholar 

  • Pratt BH, Heather WA, Shepherd CJ (1973) Recovery of Phytophthora cinnamomi from native vegetation in a remote area of New South Wales. Trans Br Mycol Soc 60: 197–204

    Google Scholar 

  • Read DJ (1991) Mycorrhizas in ecosystems. Experientia 47: 376–391

    Google Scholar 

  • Warcup JH (1950) The soil-plate method for the isolation of fungi from soil. Nature 166: 117–118

    Google Scholar 

  • Warcup JH (1951) The ecology of soil fungi. Br Mycol Soc Trans 34: 376–399

    Google Scholar 

  • West HM, Fitter AH, Watkinson AR (1993) The influence of three biocides on the fungal associates of the roots of Vulpia ciliata ssp. ambigua under natural conditions. J Ecol 81: 345–350

    Google Scholar 

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Newsham, K.K., Fitter, A.H. & Watkinson, A.R. Rhizosphere and root-infecting fungi and the design of ecological field experiments. Oecologia 102, 230–237 (1995). https://doi.org/10.1007/BF00333255

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  • DOI: https://doi.org/10.1007/BF00333255

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