Results 171 to 180 of about 3,185 (198)
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Mycoparasitism of Dispira Simplex and D. Parvispora

Mycologia, 1966
Physiological studies of the haustorium-producing, biotrophic mycoparasites have been limited primarily to two genera, Dispira and Piptocephalis. Ayers (1933, 1935) was a pioneer in the physiological study of this group of parasites and reported that the host range of Dispira cornuta Van Tiegh. was limited to several other species of Mucorales and that
M, Brunk, H L, Barnett
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Mycoparasitism: ecology and physiology

Canadian Journal of Plant Pathology, 1987
(1987). Mycoparasitism: ecology and physiology. Canadian Journal of Plant Pathology: Vol. 9, No. 4, pp. 370-379.
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CmpacC regulates mycoparasitism, oxalate degradation and antifungal activity in the mycoparasitic fungus Coniothyrium minitans.

Environmental microbiology, 2016
The PacC/Rim101 pH-responsive transcription factor is an important pathogenicity element for many plant-pathogenic fungi. In this study, we investigated the roles of a PacC homologue, CmpacC, in the mycoparasitic fungus Coniothyrium minitans. CmpacC was confirmed to have the transcriptional activation activity by the transcriptional activation test in ...
Yi, Lou   +9 more
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Mycoparasitism within the Zygomycetes

Botanical Journal of the Linnean Society, 1985
The Zygomycetes includes a number of mycoparasitic genera, which differ in their strategies of parasitism. Piptocephalis, Dispira, Dimargaris and Tieghemiomyces are typical biotrophs, and display many features associated with this mode of infection, such as the formation of haustoria.
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A Destructive Mycoparasite, Gliocladium Roseum

Mycologia, 1962
Gliocladium roseum was shown to be a destructive parasite on numerous other fungi. In fact, no fungus tested was immune to attack at all stages of development.
H. L. Barnett, V. G. Lilly
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Mycoparasitism in Basidiomycota 

Among the over 31,000 recognized species within Basidiomycota, approximately 200 are documented as parasites of other fungi, so-called mycoparasites. They exhibit a remarkable diversity in morphological characteristics, host-parasite interaction structures, and phylogenetic affiliations.
Nathan Schoutteten   +2 more
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Biotrophic mycoparasitism byVerticillium biguttatum onRhizoctonia solani

European Journal of Plant Pathology, 1994
Verticillium biguttatum cannot utilise cellulose or nitrate-nitrogen and it requires biotin for growth, yet it grew and sporulated abundantly onRhizoctonia solani on cellulose, obtaining at least organic carbon, nitrogen and biotin fromR. solani. Videomicroscopy of inter-hyphal interactions on films of water agar showed thatV.
P. H. J. F. Van Den Boogert   +1 more
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Mycoparasitism ofFusarium SPP. onRhizoctonia solani Kühn

Plant and Soil, 1980
Experiments on nutrient and staled agar were carried out to investigate the mycoparasitic activity of some fusaria againstRhizoctonia solani Kuhn. Penetration and coiling byFusarium oxysporum Sch.,F. semitectum Berk & Rav. andF. udum Butler in and around theR. solani hyphae was observed. Lysis ofF. udum hyphae was observed inside theR.
D. K. Arora, R. S. Dwivedi
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Mycoparasitism of Sclerotia of Sclerotium Cepivorum.

Australasian Plant Pathology, 1989
Four fungal species were recorded in vitro as potential mycoparasites of sclerotia of Sclerotium cepivorum, the causal agent of onion white rot. Parasitised sclerotia appeared shrunken and decayed and failed to germinate. Light and scanning electron microscopy revealed colonisation of the internal structure of the sclerotium by the mycoparasites.
A Stewart, YA Harrison
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Biology and ecology of mycoparasitism

Canadian Journal of Botany, 1995
The term mycoparasitism applies strictly to those relationships in which one living fungus acts as a nutrient source for another, but fungicolous relationships may also be included in which nutrient exchange has not been shown. Fungicolous fungi have a constant but indeterminate association with another fungus, and it can be difficult to demonstrate a
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