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The effect of small-scale environmental changes on disease incidence and severity in a natural plant-pathogen interaction

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Summary

The incidence and severity of Rhynchosporium secalis infections were assessed in a large population of Hordeum leporinum. Transects were set out in four directions from five trees to determine the effect of shading. Under the tree canopy 60.3% of H. leporinum plants were infected while only 11.2% were infected away from the canopy. Disease severity, on those plants which were infected, was higher under the canopy (mean 12.4% and 13.0% leaf area diseased for the flag and first leaves, respectively) than away from the canopy (means of 7.8% and 5.0% for the flag and first leaves respectively). Plants under the tree canopy contained on average 23% more nitrogen, raising the possibility that the susceptibility of the host changed in response to nitrogen levels. However, the observed pattern is also consistent with the hypothesis that shade-associated changes in the environment enhanced the ability of the pathogen to infect and develop on the host. The data clearly demonstrate the importance of small-scale environmental factors on natural host-pathogen interactions. These environmental factors may cause differential selection for disease resistance within a host population, which may ultimately lead to the formation of sub-populations with differing levels of resistance.

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References

  • Augspurger CK (1984) Seedling survival of tropical tree species: Interactions of dispersal distance, light-gaps, and pathogens. Ecology 65:1705–1712

    Google Scholar 

  • Augspurger CK, Kelly CK (1984) Pathogen mortality of tropical tree seedlings: Experimental studies of the effects of dispersal distance, seedling density, and light conditions. Oecologia (Berlin) 61:211–217

    Google Scholar 

  • Burdon JJ (1987) Disease and Plant Population Biology. Cambridge University Press, Cambridge

    Google Scholar 

  • Burdon JJ, Müller WJ (1987) Measuring the cost of resistance to Puccinia coronata Cda in Avena fatua L. J Appl Ecol 24:191–200

    Google Scholar 

  • Burdon JJ, Marshall DR, Brown AHD (1983) Demographic and genetic changes in populations of Echium plantagineum. J Ecol 71:667–679

    Google Scholar 

  • Caldwell RM (1937) Rhynchosporium scald of, barley, rye, and other grasses. J Agric Res (Washington DC) 55:175–198

    Google Scholar 

  • Dinoor A, Eshed N (1984) The role and importance of pathogens in natural plant communities. Ann Rev Phytopathology 22:443–466

    Google Scholar 

  • Jarosz AM (1984) Ecological and evolutionary dynamics of Phlox-Erysiphe cichoracearum interactions. Ph.D. thesis, Purdue University

  • Jarosz AM, Levy M (1988) Effects of habitat and population structure on powdery mildew epidemics in experimental Phlox populations. Phytopathology (in press)

  • Jenkins JEE, Jemmett JL (1967) Barley leaf blotch. NAAS Q Rev No 75: 127–132

    Google Scholar 

  • Lukens RJ, Mullany R (1972) The influence of shade and wet soil on southern corn leaf blight. Plant Dis Rept 56:203–206

    Google Scholar 

  • Nevo E, Moseman JG, Beiles A, Zohary D (1984) Correlations of ecological factors and allozyme variations with resistance to Erysiphe graminis hordei in Hordeum spontaneum in Israel: Patterns and Applications. Plant Syst Evol 145:79–96

    Google Scholar 

  • Nevo E, Moseman JG, Beiles A, Zohary D (1985) Patterns of resistance of Israeli wild emmer wheat to pathogens I. Predictive method by ecology and allozyme genotypes for powdery mildew and leaf rust. Genetica 67:209–222

    Google Scholar 

  • Nevo E, Gerechter-Amitai Z, Beiles A, Golenberg EM (1986) Resistance of wild wheat to stripe rust: Predictive method by ecology and allozyme genotypes. Plant Syst Ecol 153:13–30

    Google Scholar 

  • Ozoe S (1956) Studies on the Rhynchosporium scald of barley and its control. Shimane Prefectural Agric Inst Bull 1:1–122

    Google Scholar 

  • Schnathorst WC (1965) Environmental relationships in the powdery mildews. Ann Rev Phytopathology 3:343–366

    Google Scholar 

  • Shipton WA, Boyd W, Ali SM (1974) Scald of barley. Rev Plant Pathology 53:839–861

    Google Scholar 

  • Snaydon RW, Davies MS (1972) Rapid population differentiation in a mosaic environment. II. Morphological variation in Anthoxanthum odoratum Evolution 26:390–405

    Google Scholar 

  • Twine JR Williams CH (1971) The determination of phosphorus in Kjeldahl digests of plant material by automatic analysis. Comm Soil Sci Plant Anal 2:485–489

    Google Scholar 

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Jarosz, A.M., Burdon, J.J. The effect of small-scale environmental changes on disease incidence and severity in a natural plant-pathogen interaction. Oecologia 75, 278–281 (1988). https://doi.org/10.1007/BF00378609

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  • DOI: https://doi.org/10.1007/BF00378609

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