Studies on phytopathogenic and saprotrophic fungi in rush associations of Lake Glinno (NW Poland)

Mazurkiewicz-Zapalowicz, K.; Wróbel, Mariola; Silicki, Artur; Wolska, Maria

doi:10.5586/am.2006.016

Cited by 8 publications

(4 citation statements)

References 13 publications

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“…Isolating from water plants the monophagous, which are strict parasites infesting calamus and soft rush in rush communities, Adamska 2005;Mazurkiewicz-Zapałowicz et al 2006;Mazurkiewicz-Zapałowicz, Grajewski 2010) and wild sedge, testifies their expansiveness and proves that they sporulate both on wild plants and ornamental cultivars (Czerniawska, Adamska 2009).…”

Section: Discussionmentioning

confidence: 99%

Phyllosphere mycobiota on garden ponds plants

Kowalik¹

2013

Acta Mycol

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Investigations were conducted on calamus, common cattail, soft rush, yellow iris and white water lily plants in twenty ponds in Malopolska and Podkarpacie Regions. Mycobiota existing in the phyllosphere caused discolouring and necroses of leaves and shoots. 88 species of mycobiota were identified and isolated from the diseased tissues. Dominant were Alternaria alternata, Epicoccum nigrum and Isaria farinosa. Fungi of genera: Aspergillus, Botrytis, Chaetomium, Cladosporium, Fusarium, Ilyonectria, Mortierella, Mucor, Penicillium, Phialophora, Phoma, Pleustomophora, Sordaria, Trichoderma and Umbelopsis were also numerous. The monophagous and the polyphagous were identified.

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Section: Discussionmentioning

confidence: 99%

Phyllosphere mycobiota on garden ponds plants

Kowalik¹

2013

Acta Mycol

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“…In the Masurian Lake District, Durska [31] noted one species, Myrioconium scirpi, on SL, which infected 50% of the plants. Rather modest data are also reported for Glinno Lake (Western Pomerania), where the occurrence of Epicoccum nigrum was only noted on SL [32], while two species, Phyllosticta scirpi and Stagonospora schoenoplecti, caused disease symptoms on SL in Czarne Sosnowickie Lake (Łęczna-Włodawa Lake District) [33]. Low species richness of microfungi associated with SL in Poland from studies cited above could arise from what they primarily refer to as pathogenic species, while the study discussed in the current paper focused on all the micromycete species associated with SL vegetation.…”

Section: Discussionmentioning

confidence: 87%

Microscopic fungi on Schoenoplectus lacustris in Płociczno and Płociowe lakes in Drawa National Park (northwest Poland)

Mazurkiewicz-Zapalowicz

Rybińska

Łopusiewicz

2017

Acta Mycol

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In the period 2009-2011, the micromycetes causing symptoms on the leaves of Schoenoplectus lacustris (SL) from Płociczno and Płociowe lakes in Drawa National Park (DNP) were investigated. A total of 39 taxa of microscopic fungi and chromistan fungi were found. The taxonomic structure of the mycobiota was dominated by anamorphs of Ascomycota. In each year of the study, the SL fungal species richness was higher in Płociowe Lake than in Płociczno Lake. In all the years of study in both lakes, the fungal community on SL was composed of the following six dominant species: Alternaria alternata, Cladosporium herbarum, Fusarium incarnatum, F. sacchari, Gibberella avenacea, and Pleospora scirpicola. The species occurring exclusively in Płociczno Lake were Papulaspora immersa, Puccinia scirpi, and Trichothecium roseum, and those found only in Płociowe Lake were Acremoniella atra, Alternaria atra, Aspergillus niger, A. versicolor, Fusarium oxysporum, Gonatobotrys simplex, Massariosphaeria scirpina, Microascus brevicaulis, Penicillium chrysogenum, and Stagonospora aquatica. Only one confirmation of the occurrence of Puccinia scirpi and the lack of other specialized obligate parasites indicate the good health of SL in DNP. The facultative parasites, inter alia, Boeremia exigua, Chaetomium globosum, Fusarium culmorum, F. incarnatum, F. sacchari, Gibberella avenacea, and Stagonospora aquatica that are present on plants as part of the natural process of apoptosis may influence the health of SL.

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“…There were several studies on aquatic fungi associated with P. australis in freshwater (Ingold 1954, 1955, Dudka 1963, Durska 1969, Taligoola et al 1972, Apinis et al 1972a, b, Wirsel et al 2001, Luo et al 2004, Ernst 2005, Neubert et al 2006, Mazurkiewicz-Zapałowicz et al 2005, 2006, Mazurkiewicz-Zapałowicz 2010, Angelini et al 2012, Abdel-Aziz 2016b and estuarine habitats (Poon & Hyde 1998, Van Ryckegem & Verbeken 2005a, b, с, Van Ryckegem et al 2007, Abdel-Aziz 2008, rhizosphere (Nechwatal et al 2008), seeds and seedlings (Shearin et al 2018). Most of the studies were carried out in the 20 th or early 21 st century, and now many fungal names have become synonyms.…”

Section: Introductionmentioning

confidence: 99%

Checklist of fungi and fungi-like organisms on the common reed Phragmites australis

2021

ajom

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This report provides an updated checklist of fungi on the common reed Phragmites australis (Cavanilles) Trinius ex Steudel. For each fungus or fungi-like organism species, we indicate the family, the part of the plant on which the fungus was found, the geographical location, and the authors who found it. The list includes fungal species on living and dead plants in the air, soil and water environment. The list contains two kingdoms, Fungi and Chromista (fungi-like organisms). The fungus kingdom is represented by 562 species belonging to 328 genera, 143 families, 58 orders, and 21 classes in three taxonomic phyla: Mucoromycota (6 species), Ascomycota (508), Basidiomycota (48). The Chromista includes 37 species belonging to eight genera, four families, three orders, and one class under one taxonomic phylum, Oomycota. From the fungus kingdom, 230 species were discovered on leaves, 124 on leaf sheaths, 336 on stems, 75 on roots, 435 in the freshwater environment, 195 in seawater, 262 on submerged plant parts, 79 in dry soil, 324 in aerial plant parts, 321 on dead plants, and 296 on live plants. From the Chromista kingdom, six species were discovered on leaves, three on leaf sheaths, three on stems, zero on roots, 26 in freshwater, zero in seawater, five on submerged plant parts, 32 in dry soil, three in aerial parts, two on dead plants, and 37 on live plants. The maximum number of the fungal species on the reed was 33 species from the family Halosphaeriaceae (19 genera, Ascomycota) and 33 species from the family Pythiaceae (three genera, Chromista).

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Studies on phytopathogenic and saprotrophic fungi in rush associations of Lake Glinno (NW Poland)

Cited by 8 publications

References 13 publications

Phyllosphere mycobiota on garden ponds plants

Phyllosphere mycobiota on garden ponds plants

Microscopic fungi on Schoenoplectus lacustris in Płociczno and Płociowe lakes in Drawa National Park (northwest Poland)

Checklist of fungi and fungi-like organisms on the common reed Phragmites australis

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