Английская Википедия:Baeomycetales

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Шаблон:Short description Шаблон:Automatic taxobox

The Baeomycetales are an order of mostly lichen-forming fungi in the subclass Ostropomycetidae, in the class Lecanoromycetes. It contains 8 families, 33 genera and about 170 species.[1] As a result of molecular phylogenetics research published in the late 2010s, several orders were folded into the Baeomycetales, resulting in a substantial increase in the number of taxa.

Taxonomy

The family Baeomycetaceae was originally proposed by Barthélemy Charles Joseph Dumortier in 1829 (under the spelling Baeomyceae); he included two genera, Baeomyces and Calicium.[2] Baeomycetaceae was initially classified in the Lecanorales,[3][4] and Baeomycetaceae and Cladoniaceae were thought to be closely related, sharing a phylogenetic origin in Lecideaceae.[5] It was transferred to the order Helotiales based on the structure of its ascus, which is similar to those in genus Leotia.[6] However, the Helotiales consists of mostly non-lichenised fungi. The first DNA studies conducted with Baeomyces species did not suggest any phylogenetic relatedness with Leotia.[7][8] Later studies demonstrated a sister group relationship between Baeomyces and the order Ostropales, and Baeomycetales was informally suggested as a suitable name for this lineage.[9]

After additional molecular studies confirmed the placement of the Baeomycetaceae in the subclass Ostropomycetidae,[10][11] the order Baeomycetales was formally circumscribed in 2007 by H. Thorsten Lumbsch, Sabine Huhndorf, and Francois Lutzoni. They suggested that Ainoa, Baeomyces, and Phyllobaeis were exemplar genera in the order.[12] The composition of the Baeomycetales has been amended several times since its original circumscription, as molecular phylogenetic analyses have helped to resolve the phylogenetic relationships amongst its members. In 2011, the order was considered to contain two families, Baeomycetaceae and Anamylopsoraceae.[13] The latter family, proposed by Lumbsch and Thomas Lunke in 1995,[14] was later shown with molecular phylogenetics to nest within the Baeomycetaceae,[15] and is now placed in synonymy with that family.[16]

In 2018, the class Lecanoromycetes was revised using a temporal approach that uses time-calibrated chronograms to define temporal bands for comparable ranks for orders and families. In this work, the orders Arctomiales, Hymeneliales, and Trapeliales were synonymized with Baeomycetales.[17] In a later review of the use of this method for biological classification of lichens, Robert Lücking considered this merge justified.[18] This synonymy was also accepted in a 2020 review of fungal classification.[1]

Classification

According to a 2020 review on fungal classification, the Baeomycetales contain 8 families and 33 genera. The following list give the families, their taxon authority and year of publication, a brief synopsis of some major characteristics of the family, the genera in each family, and estimated number of species in each genus.[1]

Arctomiaceae Шаблон:Small[19]
Thallus crustose or fruticose, gelatinized, and with rhizoids. Arctic and subarctic distribution, usually associated with bryophytes. Photobiont partner is cyanobacterial,Шаблон:Sfn from genus Nostoc. No secondary chemicals produced.Шаблон:Sfn
Arthrorhaphidaceae Шаблон:Small[21]
Thallus either crustose, or immersed within the host. Widespread in temperate and montane regions, growth on soil, with green algal photobiont partner;Шаблон:Sfn some species are lichenicolous. Secondary chemicals are depsides and pulvinic acid derivatives.Шаблон:Sfn
Файл:Phyllobaeis imbricata.jpg
Phyllobaeis imbricata (Baeomycetaceae)
Baeomycetaceae Шаблон:Small[2]
Thallus crustose or squamulose, apothecia either sessile or sometimes on pink or brown stipes that are special extensions of the thallus that are not lichenized. Widespread distribution with growth typically on rock or soil.Шаблон:Sfn
Cameroniaceae Шаблон:Small[22]
Thallus crustose with chlorococcoid photobiont and perithecioid, immersed ascomata. Four spores per ascus. Secondary chemicals are dibenzofurans and triphenyls. Found in temperate Tasmania, growth on rocks.Шаблон:Sfn
Файл:Tremolecia atrata.jpg
Tremolecia atrata (Hymeneliaceae)
Hymeneliaceae Шаблон:Small[23]
Thallus usually crustose, lacking rhizoids, sometimes evanescent. Widespread distribution with growth usually on rocks and green algal photobiont.Шаблон:Sfn No secondary chemicals produced.Шаблон:Sfn
Protothelenellaceae Шаблон:Small[24][note 2]
Thallus crustose, but sometimes poorly developed, or even absent. Ascomata intermediate in form between apothecial and perithecial, immersed, sometimes becoming erumpent, dark green to black, and opened by a broad pore. Widely distributed in northern temperate regions. Some species grow as saprobes on bark, while others are lichenised with green algae, rarely lichenicolous.Шаблон:Sfn Subcosmopolitan distribution; habitats include acidic rocks and soil, bryophytes and detritus, wood, or other lichens. No secondary chemicals are produced.Шаблон:Sfn
Файл:Placopsis lambii - Flickr - pellaea.jpg
Placopsis lambii (Trapeliaceae)
Trapeliaceae Шаблон:Small[25]
Thallus crustose to squamulose in form. Collectively, a cosmopolitan distribution, but mostly concentrated in temperate regions. Depsides, depsidones, and anthraquinones produced as secondary chemicals.Шаблон:Sfn
Xylographaceae Шаблон:Small[26]
Thallus immersed in the wood substrate with rounded to lirellate fruiting bodies that are pale to blackening. Family resurrected for use following molecular analysis published in 2015.[15]

Notes

Шаблон:Reflist

References

Шаблон:Reflist

Cited literature

Шаблон:Taxonbar

  1. 1,0 1,1 1,2 1,3 1,4 Ошибка цитирования Неверный тег <ref>; для сносок Wijayawardene et al. 2020 не указан текст
  2. 2,0 2,1 Ошибка цитирования Неверный тег <ref>; для сносок Dumortier 1829 не указан текст
  3. Ошибка цитирования Неверный тег <ref>; для сносок Ahmadjian & Hale 1973 не указан текст
  4. Ошибка цитирования Неверный тег <ref>; для сносок Henssen & Jahns 1973 не указан текст
  5. Ошибка цитирования Неверный тег <ref>; для сносок Ahti 1982 не указан текст
  6. Ошибка цитирования Неверный тег <ref>; для сносок Tehler 1996 не указан текст
  7. Ошибка цитирования Неверный тег <ref>; для сносок Stenroos & DePriest 1998 не указан текст
  8. Ошибка цитирования Неверный тег <ref>; для сносок Platt & Spatafora 1999 не указан текст
  9. Ошибка цитирования Неверный тег <ref>; для сносок Kauff & Lutzoni 2002 не указан текст
  10. Ошибка цитирования Неверный тег <ref>; для сносок Miadlikowska et al. 2006 не указан текст
  11. Ошибка цитирования Неверный тег <ref>; для сносок Lumbsch et al. 2007b не указан текст
  12. Ошибка цитирования Неверный тег <ref>; для сносок Lumbsch et al. 2007 не указан текст
  13. Ошибка цитирования Неверный тег <ref>; для сносок Hodkinson & Lendemer 2011 не указан текст
  14. Ошибка цитирования Неверный тег <ref>; для сносок Lumbsch et al. 1995 не указан текст
  15. 15,0 15,1 Ошибка цитирования Неверный тег <ref>; для сносок Resl et al. 2015 не указан текст
  16. Ошибка цитирования Неверный тег <ref>; для сносок MycoBank: Anamylopsoraceae не указан текст
  17. 17,0 17,1 Ошибка цитирования Неверный тег <ref>; для сносок Kraichak et al. 2018 не указан текст
  18. Ошибка цитирования Неверный тег <ref>; для сносок Lücking 2019 не указан текст
  19. Ошибка цитирования Неверный тег <ref>; для сносок Fries 1861 не указан текст
  20. Ошибка цитирования Неверный тег <ref>; для сносок Ertz et al. 2017 не указан текст
  21. Ошибка цитирования Неверный тег <ref>; для сносок Poelt & Hafellner 1976 не указан текст
  22. Ошибка цитирования Неверный тег <ref>; для сносок Lumbsch et al. 2012 не указан текст
  23. Ошибка цитирования Неверный тег <ref>; для сносок Körber 1855 не указан текст
  24. Ошибка цитирования Неверный тег <ref>; для сносок Mayrhofer & Poelt 1985 не указан текст
  25. Ошибка цитирования Неверный тег <ref>; для сносок Hertel 1970 не указан текст
  26. Ошибка цитирования Неверный тег <ref>; для сносок Tuckerman 1888 не указан текст


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