Heliocybe Explained

Heliocybe is an agaric genus[1] closely allied to Neolentinus and the bracket fungus, Gloeophyllum, all of which cause brown rot of wood.[2] [3] Heliocybe sulcata, the type and sole species, is characterized by thumb-sized, tough, revivable, often dried, mushroom fruitbodies, with a tanned symmetric pileus that is radially cracked into a cartoon sun-like pattern of arranged scales and ridges, distant serrated lamellae, and a scaly central stipe. Microscopically it differs from Neolentinus by the absence of clamp connections. Like Neolentinus, it produces abundant, conspicuous pleurocystidia. Heliocybe sulcata typically fruits on decorticated, sun-dried and cracked wood, such as fence posts and rails, vineyard trellises in Europe, branches in slash areas, and semi-arid areas such on sagebrush or on naio branches in rain shadow areas of Hawaii, or in open pine forests.[4] [5] [6] [7] __TOC__

Etymology

Heliocybe derives from the Greek helios (= the sun) and cybe (=head), and means "the sun-head". It was coined in reference to its sun-like pattern on its pileus together with its affinity to sun-baked habitats.

Classification

In older classifications, H. sulcatahttps://web.archive.org/web/20071010102253/http://www.minnesotamushrooms.org/news/2004-02/mush-science.htm was known as Lentinus sulcatus or Panus fulvidus. However, there is strong phylogenetic evidence for the segregation of a group of brown rot causing fungi at the level of order, including Neolentinus and Heliocybe and Gloeophyllum, from the Polyporales where Lentinus and Panus are classified.[2] [3] [8] [9] [10] Heliocybe has also been placed into synonymy with Neolentinus, but anatomically they differ by the absence versus the presence of clamp connections[1] and phylogenetically Heliocybe is distinct, being either a sister group to Neolentinus or to a Neolentinus-Gloeophyllum-clade, or allied to Gloeophyllum odoratum.[2] [3] [9] [10]

Notes and References

  1. Redhead, S.A. . Ginns, J.H.. 1985. A reappraisal of agaric genera associated with brown rots of wood. Trans. Mycol. Soc. Japan. 26. 349–381.
  2. Thorn, R.G.. 2000. Phylogenetic analyses and the distribution of nematophagy support monophyletic Pleurotaceae within the polyphyletic pleurotoid-lentinoid fungi. Mycologia. 92. 241–252. 10.2307/3761557 . 3761557 . 2 . Mycologia, Vol. 92, No. 2. etal.
  3. Hibbett, D.S. . Donoghue, M.J.. 2001. Analysis of character correlations among wood decay mechanisms, mating systems, and substrate ranges in Homobasidiomycetes. Syst. Biol.. 50. 215–242. 10.1080/10635150151125879 . 12116929 . 2.
  4. Redhead, S.A.. 1989. A biogeographical overview of the Canadian mushroom flora. Can. J. Bot.. 67. 3003–3062. 10.1139/b89-384 . 10.
  5. Schalkwijk-Barendsen, H.M.E.. 1991. Mushrooms of western Canada.
  6. Evenson, V.S.. 1997. Mushrooms of Colorado and the southern Rocky Mountains.
  7. Hemmes, D.E. . Desjardin, D.E.. 2002. An identification guide – mushrooms of Hawai'i.
  8. Hibbett, D.S. . Binder, M.. 2002. Evolution of complex fruiting-body morphologies in homobasidiomycetes. Proc. R. Soc. Lond. B. 269. 1963–1969. 10.1098/rspb.2002.2123 . 12396494 . 1504 . 1691125.
  9. Binder, M.. 2005. The phylogenetic distribution of resupinate forms across the major clades of mushroom-forming fungi (Homobasidiomycetes). Syst. Biodivers.. 3. 113–157. 10.1017/S1477200005001623 . 2. 13102957 . etal.
  10. García-Sandoval R . Wang Z . Binder M . Hibbett DS. . 2011. Molecular phylogenetics of the Gloeophyllales and relative ages of clades of Agaricomycotina producing a brown rot. Mycologia. 103. 510–524. 10.3852/10-209 . 21186327 . 3 . 9801943 .