Rajchenberg, Mario; Pildain, María Belén; de Errasti, Andrés; Riquelme, Cristian; Becerra, José; Torres-Díaz, Cristian; Cabrera-Pardo, Jaime R. 2021: Species and genera in Aleurodiscus sensu lato as viewed from the Southern Hemisphere. Mycologia 113: 1264-1277.
Details
Rajchenberg, Mario; Pildain, María Belén; de Errasti, Andrés; Riquelme, Cristian; Becerra, José; Torres-Díaz, Cristian; Cabrera-Pardo, Jaime R. 2021: Species and genera in Aleurodiscus sensu lato as viewed from the Southern Hemisphere. Mycologia 113: 1264-1277.
10.1080/00275514.2021.1940671
Article
Taxonomic concepts
Aleurocystidiellum subcruentatum (Berk. & M.A. Curtis) P.A. Lemke
Aleurodiscus disciformis (DC.) Pat.
Aleurodiscus limonisporus D.A. Reid 1956 [1955]
Aleurodiscus mirabilis (Berk. & M.A. Curtis) Höhn. 1909
Aleurodiscus parmuliformis G. Cunn. 1956
Aleurodiscus weirii Burt
Aleurodiscus zealandicus (Cooke & W. Phillips) G. Cunn. 1953 [1952]
Chaetocypha zealandica (Cooke & W. Phillips) Kuntze
Cyphella zealandica Cooke & W. Phillips
Gloeosoma mirabile (Berk. & M.A. Curtis) Rajchenb., Pildain & Riquelme
Gloeosoma zealandicum (Cooke & W. Phillips) Rajchenb., Pildain & Riquelme
Psilopezia mirabilis Berk. & M.A. Curtis
Stereodiscus limonisporus (D.A. Reid) Rajchenb. & Pidain
Stereodiscus parmuliformis (G. Cunn.) Rajchenb. & Pildain
Descriptions
Remarks: Gloeosoma was defined as a taxon growing on dead branches of Nothofagaceae in Patagonia and remained monotypic over the years. A lack of information on G. vitellinum in phylogenetic studies precluded any conclusion regarding its taxonomic sta-tus. It was a matter of personal decision whether to accept the genus or consider it a synonym of Aleurodis-cus, as the microscopic features were quite typical of the latter in a broad sense.
Our study includes sequences of G. vitellinum for the first time and shows that together with G. zealandicum, G. mirabile, and Gloeosoma decor-ticans, sp. nov. (described below), they form a well- defined group of species with strong phylogenetic sup-port. This group clustered in the Stereaceae clade but was distant from A. amorphus (Pers.) J. Schröt., the type species of Aleurodiscus. The latter differs from Gloeosma morphologically by the simple-septate generative hyphae.
Our study includes sequences of G. vitellinum for the first time and shows that together with G. zealandicum, G. mirabile, and Gloeosoma decor-ticans, sp. nov. (described below), they form a well- defined group of species with strong phylogenetic sup-port. This group clustered in the Stereaceae clade but was distant from A. amorphus (Pers.) J. Schröt., the type species of Aleurodiscus. The latter differs from Gloeosma morphologically by the simple-septate generative hyphae.
Remarks: Stereodiscus is characterized by smooth, thin-walled, cylindric, broadly ellipsoid to citriform basidiospores up to 25 μm long and absence of any of the typical cystidia in Aleurodiscus s. lat., i.e., acantho-cystidia, acanthophyses, gloeocystidia, and dendrohy-phidia, but with skeletocystidia present in three species (S. antarcticus, S. parmuliformis, and S. trivialis). The hyphal system is monomitic with simple-septate hyphae, except in the recently described S. patagonicus (as Aleu-rodiscus), which features scattered clamps on the hyphae and at the bases of basidia (Phookamsak et al. 2019). The latter is consistent with its phylogenetic position, as it is excluded from the main cluster of species (FIG. 1). Otherwise, the five species grouped with strong support.
Stereodiscus is most closely related to Gloeosoma (FIG. 1). Gorjón et al. (2013) suggested the cluster of Aleurodiscus antarcticus, A. parmuliformis, and A. trivialis warranted segregation at the genus level characterized by possession of simple-septate hyphae and presence of skeletocystidia and geographic distribu-tion occurring only in the Southern Hemisphere. Our analyses show that two other taxa are included in this group, widening its morphological definition, and it indeed deserves generic rank.
Stereodiscus is most closely related to Gloeosoma (FIG. 1). Gorjón et al. (2013) suggested the cluster of Aleurodiscus antarcticus, A. parmuliformis, and A. trivialis warranted segregation at the genus level characterized by possession of simple-septate hyphae and presence of skeletocystidia and geographic distribu-tion occurring only in the Southern Hemisphere. Our analyses show that two other taxa are included in this group, widening its morphological definition, and it indeed deserves generic rank.
Cited scientific names
- Acanthobasidium weirii (Burt) L.D. Dai & S.H. He 2016
- Aleurocystidiellum disciforme (DC.) Boidin, Terra & Lanq. 1968
- Aleurocystidiellum subcruentatum (Berk. & M.A. Curtis) P.A. Lemke 1964
- Aleurodiscus disciformis (DC.) Pat. 1894
- Aleurodiscus limonisporus D.A. Reid 1956 [1955]
- Aleurodiscus mirabilis (Berk. & M.A. Curtis) Höhn. 1909
- Aleurodiscus parmuliformis G. Cunn. 1956
- Aleurodiscus weirii Burt 1918
- Aleurodiscus zealandicus (Cooke & W. Phillips) G. Cunn. 1953 [1952]
- Chaetocypha zealandica (Cooke & W. Phillips) Kuntze 1891
- Cyphella zealandica Cooke & W. Phillips 1879
- Gloeosoma Bres. 1920
- Gloeosoma mirabile (Berk. & M.A. Curtis) Rajchenb., Pildain & Riquelme 2021
- Gloeosoma zealandicum (Cooke & W. Phillips) Rajchenb., Pildain & Riquelme 2021
- Psilopezia mirabilis Berk. & M.A. Curtis 1868 [1869]
- Stereodiscus limonisporus (D.A. Reid) Rajchenb. & Pidain 2021
- Stereodiscus parmuliformis (G. Cunn.) Rajchenb. & Pildain 2021
- Stereodiscus Rajchenb. & Pildain 2021
Metadata
89d0fc8d-fa23-4f87-ba71-e18195aacf62
reference
Names_Fungi
2 September 2021
5 July 2022