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Marchandiomyces lignicola (holotype). (A) Sclerotia in optical section (in Congo red). (B) Sclerotia, surface view (in LCB, the stain only penetrated the external cells of the sclerotium). (C) Squash preparation of sclerotia (in Congo red, with phase contrast). (D) Squash preparation of sclerotia (in LCB). Bars: A, B and D = 20 m m ; C = 10 m m. 

Marchandiomyces lignicola (holotype). (A) Sclerotia in optical section (in Congo red). (B) Sclerotia, surface view (in LCB, the stain only penetrated the external cells of the sclerotium). (C) Squash preparation of sclerotia (in Congo red, with phase contrast). (D) Squash preparation of sclerotia (in LCB). Bars: A, B and D = 20 m m ; C = 10 m m. 

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... Since the abundance of the unidentified Heliotiales was insignificant in the untreated material and negative control, it is believed that its growth was particularity favored by the conditions in the fungal pretreated samples, possibly the feedstock composition changes caused by C. subvermispora. In the case of Marchandiomyces (a basidiomycete), one common species of this genus is M. lignicola, a woodinhabiting lignicolous fungus (Depriest et al. 2005). However, it is uncertain if this was the fungal species detected, and how it could have affected the delignification during the fungal pretreatment or its interaction with C. subvermispora. ...
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... In addition to our newly generated sequence (GenBank accession: Corticium sp. ITS and nuLSU: MH520061), we included sequences used in earlier analyses of the Corticiales (Sikaroodi et al. 2001;DePriest et al. 2005;Lawrey et al. 2007Lawrey et al. , 2008Ghobad-Nejhad & Hallenberg 2011;Ghobad-Nejhad et al. 2010) and those from a broad range of taxa representing recognized clades in the Corticium clade (Langer 2002;Larson 2004;Binder et al. 2005;Hibbett et al. 2007Hibbett et al. , 2014Larson et al. 2007;Diederich et al. 2011). We had difficulty aligning ITS sequences available in GenBank, so we trimmed our sequence to include only the nuLSU and used only published nuLSU sequences from Gen-Bank in our analyses. ...
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Agaricomycetes includes ca. 21,000 described species of mushroom-forming fungi that function as decayers, pathogens, and mutualists in both terrestrial and aquatic habitats. The morphological diversity of Agaricomycete fruiting bodies is unparalleled in any other group of fungi, ranging from simple corticioid forms to complex, developmentally integrated forms (e.g., stinkhorns). In recent years, understanding of the phylogenetic relationships and biodiversity of Agaricomycetes has advanced dramatically, through a combination of polymerase chain reaction-based multilocus phylogenetics, phylogenomics, and molecular environmental surveys. Agaricomycetes is strongly supported as a clade and includes several groups formerly regarded as Heterobasidiomycetes, namely the Auriculariales, Sebacinales, and certain Cantharellales (Tulasnellaceae and Ceratobasidiaceae). The Agaricomycetes can be divided into 20 mutually exclusive clades that have been treated as orders. This chapter presents an overview of the phylogenetic diversity of Agaricomycetes, emphasizing recent molecular phylogenetic studies.
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Root rot, caused by Fusarium avenaceum (teleomorph: Gibberella avenacea), is an important disease of lupin (Lupinus angustifolius) and other crops in western Canada. Fusarium isolates collected from infected roots of lupin in central Alberta were characterized using two RAPD primers, three microsatellite-primed PCR markers, diagnostic primers for putative mating type, sequence comparison of the translation elongation factor 1α (EF1α) and internal transcribed spacer (ITS) region, and assessments of aggressiveness on lupin seedlings. The teleomorph phase of F. avenaceum has been reported only twice in the world, but both mating types were found throughout the province. Isolates of mating type 2 were slightly more aggressive than mating type 1 on five lupin cultivars. All 42 isolates of F. avenaceum assessed in this study had a unique multilocus genotype, which indicates a high level of genotypic diversity in the pathogen population. Cluster analysis did not reveal an association between the geographic location of the isolates and genetic relatedness based on genetic markers. Instead, the F. avenaceum isolates divided into two distinct groups, with isolates from both groups occurring together at many sites. Phylogenetic analysis also revealed high diversity and the presence of some European-like isolates within the Canadian pathogen population. The high genotypic diversity of isolates and the presence of both mating types across sites provide an indication that sexual reproduction may occur within populations of F. avenaceum in Alberta.