Two endoconidial, black meristematic fungi, Celosporium larixicolum gen. et sp. nov. (Dothideales) and Hispidoconidioma alpina gen. et sp. nov. (Capnodiales) are described from black subicula on twigs of declining larch ( Larix lyallii Parl) trees in Alberta, Canada. Conidioma morphology and phylogenetic analysis of LSU and ITS regions indicate that these taxa are both distinct from each other and from previously described endoconidial genera. Conidiomata of C. larixicolum consist of black cellular clumps (aggregated conidiogenous cells) that are either naked or enveloped by scant to dense mycelium that sometimes organizes into a cupulate peridium. Endoconidia are 1–3 celled, hyaline when released but become pigmented as they age, and very variable in size and shape, e.g., globose, pear-shaped, osteoid, or discoid with an irregular flange. In H. alpina, colonies are three-layered, consisting of a central pseudoparenchymatous layer sandwiched between an upper and a basal hyphal layers, and conidiogenesis occurs in sporadic areas of the central layer. Endoconidia are unicellular, hyaline, and subglobose to ellipsoid. The strong phylogenetic affinities between these newly described taxa and slow-growing, melanized fungi isolated from rocks suggest individual black meristematic fungus lineages may have broad habitat ranges.

The host-endophyte interaction between roots of aspen (Populus tremuloides) and Cryptosporiopsis radicicola was examined primarily by transmission electron microscopy. Hyphae growing on the exterior of the inoculated roots had a thick, electron-dense, adhesive sheath. At hyphal contact and penetration, host epidermal cells exhibited a series of defense responses (viz. formation of papillae and partition walls, general wall thickening and walling-off of internal hyphae). In papilla formation, loop-shaped, rough endoplasmic reticula (rER) gave rise to globose secretory vesicles that accumulated around and then fused to the developing papilla. Unlike papillae, general wall thickening was associated with the Golgi apparatus (GA) that produced cell wall materials; 1-3 layers of Golgi cisternae were in contact with or in the immediate proximity (mostly within 0-0.5 microm) of and lying parallel to the host cell wall, where they budded out numerous subglobose vesicles that fused directly to the host cell wall and made it thicker. Partition wall formation and walling-off of internal hyphae also were common; the former was associated with an extended single cisterna, which was indistinguishable from rER or individual cisternae of GA, and in the latter phenomenon internal hyphae were encased by electron-dense material containing numerous ribosomes and membranous elements that were derived apparently from proliferated rER. These pronounced defense responses protected the stele and contributed to making C. radicicola endophytic rather than pathogenic.

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A new endoconidial taxon, Endophoma elongata gen. et sp. nov., isolated from bat-cave soil, is reported from Alberta, Canada. It is morphologically unique in producing two forms of unilocular, endoconidial conidiomata (i.e. a superficially Phoma-like spherical, often ostiolate form and a cylindrical, non-ostiolate, often setose cleistopycnidial form). Locules of both forms are pseudoparenchymatous, filled with hyaline, thin-walled, endoconidial conidiogenous cells. Endoconidia are hyaline and unicellular. One- or two-celled chlamydospores are abundant in culture. Phylogenetic analysis of the LSU, ITS and β-tubulin regions indicates Endophoma is a member of the Didymellaceae and remote from all other endoconidial genera. Endoconidiogenesis has not been reported previously within the Didymellaceae, and Endophoma represents the first report of a coelomycetous, endoconidial genus in the Pleosporales.