Plant Ecology and Evolution 151(2): 278-283, doi: 10.5091/plecevo.2018.1442
Factors affecting the local distribution of Polystigma rubrum stromata on Prunus spinosa
expand article infoHattie R. Roberts, Sara E. Pidcock, Sky C. Redhead, Emily Richards, Kevin O’Shaughnessy, Brian Douglas§, Gareth Wyn Griffith|
‡ Institute of Biological, Environmental and Rural Sciences, Cledwyn Building, Aberystwyth University, Penglais, Aberystwyth, Ceredigion Wales SY23 3DD, United Kingdom§ Jodrell Laboratory, Royal Botanic Gardens, Kew, Surrey, England TW9 3DS, United Kingdom| Aberystwyth University, Aberystwyth, United Kingdom
Open Access
Abstract

Background and aimsPolystigma rubrum forms orange-red stromata on the surface of living leaves of Prunus spinosa and P. domestica. Records suggests that this fungus now has a much more limited distribution in Britain than recorded in the 19th and early 20th century.

Methods – We studied the local distribution of the fungus in the Burren Hills of western Ireland where it remains very common.

Key results – Assessment of the local distribution of the fungus over two years found stromata to occur more frequently on P. spinosa leaves in hedgerows than woodlands. On individual trees in areas of open limestone pavement, the frequency of stromata was ten times higher in 2016 than 2015, possibly related to interannual rainfall differences. On hedgerow trees subjected to winter flooding, stromata were much less abundant, whereas stromata were more abundant on leaves also infected by the gall mite Eriophyes prunispinosae. The identity of Po. rubrum was confirmed by ITS sequencing.

Conclusion – At a field location where Po. rubrum stromata are present in unusually high abundance, the distribution of stromata on trees in different habitats showed high levels of variation linked to both habitat and the presence of gall mites. Further work is required to determine whether variation in leaf surface and soil moisture are the key determinants of the observed distribution. Such investigations may reveal why Po. rubrum, once common in northern Europe is now restricted mainly to westerly, coastal locations.

Keywords
Ascomycete taxonomy, endophyte, fungal conservation, leaf pathogen, Xylariales, biotrophs, Polystigma rubrum

References

  • Aylor D.E., Sutton T.B. (1992) Release of Venturia inaequalis ascospores during unsteady rain: Relationship to spore transport and deposition. Phytopathology 82: 532–540. https://doi.org/10.1094/Phyto-82-532
  • Chinery M. (2013) Britain’s plant galls: a photographic guide. Princeton, Princeton University Press.
  • Dayarathne M., Maharachchikumbura S., Jones E., Goonasekara I., Bulgakov T., Al-Sadi A.M., Hyde K.D., Lumyong S., McKenzie E.H.C. (2017) Neophyllachora gen nov.(Phyllachorales), three new species of Phyllachora from Poaceae and resurrection of Polystigmataceae (Xylariales). Mycosphere 8: 1598–1625. https://doi.org/10.5943/mycosphere/8/10/2
  • Díaz R., Zas R., Fernández-López J. (2007) Genetic variation of Prunus avium in susceptibility to cherry leaf spot (Blumeriella jaapii) in spatially heterogeneous infected seed orchards. Annals of Forest Science 64: 21–30. https://doi.org/10.1051/forest:2006084
  • Douglas B. (2018) Lost and Found Fungi Datasheet: Polystigma rubrum. Available from http://fungi.myspecies.info/sites/fungi.myspecies.info/files/Polystigma%20rubrum.pdf [accessed 20 Jun. 2018].
  • Evans S., Henrici A., Ing B. (2006) Red data list of threatened British fungi. Report by the British Mycological Society (BMS), working with the Joint Nature Conservation Committee. Available from http://www.britmycolsoc.org.uk/mycology/conservation/red-data-list/ [accessed 20 Jun. 2018].
  • Gadoury D.M., MacHardy W.E. (1986) Forecasting ascospore dose of Venturia inaequalis in commercial apple orchards. Phytopathology 76: 112–118. https://doi.org/10.1094/Phyto-76-112
  • Gispert C., Oldfield G.N., Perring T.M., Creamer R. (1998) Biology of the transmission of peach mosaic virus by Eriophyes insidiosus (Acari: Eriophyidae). Plant Disease 82: 1371–1374. https://doi.org/10.1094/PDIS.1998.82.12.1371
  • Grove W.B. (1884) Memoirs: some account of Polystigma rubrum Pers. based upon the recent investigations of Dr. AB Frank and C. Fisch. Journal of Cell Science 2: 328–334.
  • Kranz J. (1962) Plant diseases in Cyrenaica. FAO Plant Protection Bulletin 10: 121–125.
  • Mardones M., Trampe-Jaschik T., Oster S., Elliott M., Urbina H., Schmitt I., Piepenbring M. (2017) Phylogeny of the order Phyllachorales (Ascomycota, Sordariomycetes): among and within order relationships based on five molecular loci. Persoonia 39: 74–90. https://doi.org/10.3767/persoonia.2017.39.04
  • Mitre jr I., Tripon A., Mitre I., Mitre V. (2015) The response of several plum cultivars to natural infection with Monilinia laxa, Polystigma rubrum and Stigmina carpophila. Notulae Scientia Biologicae 7: 136.
  • O’Connor J.P. (2004) A review of the Irish gall-wasps (Hymenoptera: Cynipidae) with notes on the gall-midges (Diptera: Cecidomyiidae) and gall-mites (Acarina: Eriophyoidea). The Irish Naturalists’ Journal 27: 335–343.
  • Ripka G. (2007) Checklist of the eriophyoid mite fauna of Hungary (Acari: Prostigmata: Eriophyoidea). Acta Phytopathologica et Entomologica Hungarica 42: 59–142. https://doi.org/10.1556/APhyt.42.2007.1.7
  • Roon D.A., Wipfli M.S., Wurtz T.L. (2014) Effects of invasive European bird cherry (Prunus padus) on leaf litter processing by aquatic invertebrate shredder communities in urban Alaskan streams. Hydrobiologia 736: 17–30. https://doi.org/10.1007/s10750-014-1881-x
  • Suzuki Y., Tanaka K., Hatakeyama S., Harada Y. (2008) Polystigma fulvum, a red leaf blotch pathogen on leaves of Prunus spp., has the Polystigmina pallescens anamorph/andromorph. Mycoscience 49: 395–398. https://doi.org/10.1007/S10267-008-0434-4