Conioscypha | |
---|---|
Scientific classification | |
Kingdom: | |
Division: | |
Class: | |
Order: | |
Family: | |
Genus: | Conioscypha Höhn. [1] |
Type species | |
Conioscypha lignicola [2] |
Conioscypha is a genus of terrestrial and freshwater fungi in the monotypic family Conioscyphaceae and the monotypic order Conioscyphales. [3] They are found on decayed wood, leaves, or bamboo stems. [4] Except for Conioscypha japonica which was isolated from dog skin fragments and hair in 2017. [5]
Austrian mycologist and lichenologist Franz Xaver Rudolf von Höhnel (1852–1920) in 1904, created the genus Conioscypha with Conioscypha lignicolaHöhn. as the generic type, which was found on submerged wood of Carpinus sp. in Austria. [1]
Then in 1973, American mycologist Carol A.Shearer reviewed and re-described Conioscypha lignicola based on type specimens together with a new of species Conioscypha variaShearer which was found on 2 balsa wood blocks submerged in the Patuxent River, Maryland, USA. [6]
Later, nine more Conioscypha species were recognized: Conioscypha bambusicolaMatsush. (Matsushima 1975), [7] [8] Conioscypha japonicaUdagawa & Toyaz. (Udagawa and Toyazaki 1983), [9] Conioscypha hoehneliiP.M. Kirk (Kirk 1984), [10] Conioscypha fabiformisMatsush. (Matsushima 1993), [11] Conioscypha dimorphaMatsush. (Matsushima 1996), [12] Conioscypha taiwanianaJ.L. Chen & Tzean (Chen and Tzean 2000), [13] Conioscypha minutisporaHern.-Restr., Gené & Guarro (Crous et al. 2014), while Zelski et al. (2015) described Conioscypha peruensisZelski, Raja, A.N. Mill. & Shearer, [14] and Conioscypha gracilis(Munk) Zelski, Raja, A.N. Mill. & Shearer, [14] with their sexual morphs. Most of the previously described species of Conioscypha were described and reported from decaying plant materials (i.e., dead wood, bamboo and leaves) derived from terrestrial and aquatic habitats. [4] Conioscypha japonica was isolated from skin scrapings and hair of a male dog (Udagawa and Toyazaki 1983). [9] [5]
In 2004, the genus Conioscyphascus was introduced based on Conioscyphascus variusRéblová & Seifert, it was named as the sexual morph of Conioscypha varia(Réblová and Seifert 2004). [4] [5]
The Conioscypha clade, based on molecular data, was considered as Ascomycota incertae sedis with genera Conioscypha and Conioscyphascus considered congeneric (Réblová and Seifert, 2004, [4] Zelski et al., 2015 [14] ) with Conioscypha accepted as the recommend name under the one name protocol (Réblová et al. 2016a). [15] According to recent changes in the ICN (McNeill et al. 2012), specifically the new article 59.1, as of January 2013, [16]
Then in a phylogenetic study of the Hypocreomycetidae, Sordariomycetes, Conioscyphales was then proposed as a new order and it was closely related to the Savoryellales order (Boonyuen et al., 2011, [17] Réblová et al., 2012, [18] Réblová et al., 2016b). [19]
Based on in vitro experiments and molecular DNA data, Réblová & Seifert (2004a) introduced Conioscyphascus, typified by Ca. varius, to accommodate holomorphs with Conioscypha asexual morphs. [4] Another sexual-asexual relationship was established for C. peruviana (Zelski et al. 2015). [14] Following the abolishment of dual nomenclature and adoption of one fungus, one name, Conioscyphascus was accepted as a synonym of Conioscypha (Zelski et al. 2015, [14] Réblová et al. 2016c). [20] Although C. gracilis is the only species of the genus known in its sexual state, the presence of typical conidia on the host near ascomata was repeatedly observed (Réblová & Seifert 2004a, Zelski et al. 2015). Conioscypha varia Shearer is illustrated for the sexual morph and C. tenebrosa is illustrated for the asexual morph, in this entry. [2]
The fungal genus is characterized dematiaceous (black yeast), unicellular, thick-walled, globose to subglobose shaped conidia produced from discrete, hyaline (transparent), 'cup-shaped' conidiogenous cells which proliferate per currently, and are lacking conidiophores (conidia, which are borne on specialized stalks). [21]
They have an unusual mode of conidiogenesis which includes aspects of both phialidic (A type of conidiogenous cell, bottle-shaped, that produces blastic conidia (phialospores) in basipetal succession) and annellidic (the conidiogenous cell (also called an annellide) produces a basipetal sequence of conidia called annelloconidia or annellospores) ontogeny (Shearer 1973, [6] Shearer & Motta 1973, [22] Cole & Samson 1979, [23] ). [4]
Conioscypha is characterized by a unique mode of conidiogenesis with blastic conidia produced at inconspicuous loci along the hyphae (Shearer 1973). [6] Traditionally, the conidia were thought to be produced from 'phialidic' conidiogenous cells (Goh & Hyde 1998). [21] Shearer & Motta (1973) [22] described Conioscypha conidiogenesis to be both 'phialidic' and 'annelidic' (Shearer & Motta 1973), [22] but Minter et al. (1983) did not agree with this observation. [24] Cole & Samson (1979) reported conidial development to be intermediate between the 'phialidic' and 'annelidic' process and after repetitive basipetal conidial secession, the remains of the outer wall of conidia collect centripetally on the conidiogenous cells to form 'collarettes'. [23]
Conidiogenesis occurs at inconspicuous loci along hyphae; a basipetal (chain of conidia in which new spores are formed at the base) succession of blastically produced conidia leave behind conspicuous collarettes that are remnants of the initial outer wall of the conidia; these accumulate centripetally to form a multi-layered collarette appearing similar to annellations (Goh & Hyde 1998). [4]
It has a cosmopolitan distribution, worldwide. [25] Including places such as Peru, [14] America (including Chesapeake Bay, [6] ) the British Isles, [10] [26] Spain, [27] China, [28] [29] Japan, [30] Thailand, [5] [29] and Taiwan. [13]
Such as; Conioscypha hoehnelii was found on bark of Eucalyptus sp. as well as the wood, and leaves of Phormium tenax J. R. & G. Forst (Agavaceae) collected in the British Isles. [10] Also Conioscypha peruviana was isolated from submerged woody debris collected in streams, rivers and a swamp in Peru. [14] Conioscypha varia has been found in indoor environments, [31] while Conioscypha minutispora has been found on dead wood in Spain. [27] Conioscypha pleiomorpha, is commonly found in association with decaying wood substrates, and might preferentially degrade lignin-enriched organic material. [5]
There was 16 morphological species (described by Liu et al. 2019b) in 2019. [28] Then 18 species, as accepted by Species Fungorum; [32]
Former species;
The order Sordariales is one of the most diverse taxonomic groups within the Sordariomycetes.
The Dactylosporaceae or Sclerococcaceae are a family of lichen-forming fungi in the class Eurotiomycetes. It is the only family of the order Sclerococcales and subclass Sclerococcomycetidae.
The Trichosphaeriales are an order of sac fungi. It is monotypic, and consists of the single family, the Trichosphaeriaceae. In 2017, the family of Trichosphaeriaceae was placed in Diaporthomycetidae families incertae sedis, which was accepted by Wijayawardene et al. (2018), and Wijayawardene et al. 2020. The order of Trichosphaeriales was also unplaced. They are generally saprobic and pathogenic on plants, commonly isolated from herbivore dung.
Conioscyphascus is a fungal genus in the Sordariomycetes class of the Ascomycota. The relationship of this taxon to other taxa within the class is unknown, and it has not yet been placed with certainty into any order or family. The genus, Conioscyphascus contains the single species Conioscyphascus varius, described as new to science in 2004. Until Conioscyphascus gracilis(Munk) Réblová & Seifert was found later in 2004.
Annulatascus is a genus of fungi in the Annulatascaceae family of the Ascomycota. The relationship of this taxon to other taxa within the Sordariomycetes class is unknown, and it has not yet been placed with certainty into any order. The genus is characterized by taxa that are saprobic on submerged, decaying plant material in freshwater habitats. Morphologically the taxa possess dark brown to black perithecia, long tapering hyaline septate paraphyses, eight-spored asci with relatively massive J− apical rings, and ascospores that may or may not possess gelatinous sheaths or appendages. There are currently 17 species included in the genus.
Glomerellales is an order of ascomycetous fungi within the subclass Hypocreomycetidae (Sordariomycetes). The order includes saprobes, endophytes and pathogens on plants, animals and other fungi with representatives found all over the world in varying habitats.
The Stachybotryaceae are a family of fungi in the order Hypocreales; the genera it contains have been described as "hyper-diverse".
Volutella is a genus of fungi belonging to the family Nectriaceae.
Dictyosporium is the type genus of fungi belonging to the family Dictyosporiaceae. By an estimate in 2018 it is formed by 45 species.
Savoryellomycetidae is a subclass of sac fungi within the class of Sordariomycetes. It contains 4 known orders of Conioscyphales, Fuscosporellales, Pleurotheciales and Savoryellales.
Conioscyphales is an order of freshwater and terrestrial fungi within the division Ascomycota. It is in the subclass Savoryellomycetidae and the class Sordariomycetes and the subdivision of Pezizomycotina.
Fuscosporellales is an order of fungi within the phylum of Ascomycota and in the class Sordariomycetes and subdivision of Pezizomycotina.
Savoryellaceae is a family of aquatic based fungi. It is the only family in the monotypic order Savoryellales within the class Sordariomycetes, division Ascomycota.
Savoryella is a genus of freshwater and marine based fungi in the family Savoryellaceae and the order Savoryellales.
Pleurotheciaceae is a family of ascomycetous fungi within the monotypic order of Pleurotheciales in the subclass Savoryellomycetidae and within the class Sordariomycetes.
Pleurothecium is a genus of terrestrial and freshwater fungi in the family Pleurotheciaceae and the monotypic order Pleurotheciales. It is typified by Pleurothecium recurvatum as the type species (Morgan) Höhn, which has the synonym of Carpoligna pleurotheciiF.A. Fernández & Huhndorf, Mycologia 9: 253. 1999.
The Torpedosporales are an order of marine based fungi in the class Sordariomycetes, subclass Hypocreomycetidae. Most are found on wood substrates in the water.
Juncigenaceae is a family of ascomycetous marine based fungi within the order of Torpedosporales in the subclass Hypocreomycetidae and within the class Sordariomycetes. They are saprobic to intertidal wood, within mangrove forests and other herbaceous wood and roots, bark, leaves in various marine habitats.
Torpedosporaceae is a monotypic family of ascomycetous marine based fungi within the order of Torpedosporales in the subclass Hypocreomycetidae and within the class Sordariomycetes. They are saprobic on intertidal mangrove wood and roots, bark leaves, and sand in various marine habitats.
Falcocladium is a genus of fungi, within the monotypic family FalcocladiaceaeSomrith., E.B.G. Jones & K.L. Pang, and within the monotypic order FalcocladialesR.H. Perera, Maharachch., Somrith., Suetrong & K.D. Hyde, within the class Dothideomycetes. They are saprobic on leaf litter, including the leaves of Eucalyptus grandis and Eucalyptus camaldulensis in tropical and terrestrial habitats.
{{cite book}}
: CS1 maint: location missing publisher (link){{cite book}}
: CS1 maint: location missing publisher (link)