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Pertusariales

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Pertusariales
Pertusaria pertusa
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Fungi
Division: Ascomycota
Class: Lecanoromycetes
Subclass: Ostropomycetidae
Order: Pertusariales
M.Choisy ex D.Hawksw. & O.E.Erikss. (1986)
Families

Agyriaceae
Coccotremataceae
Icmadophilaceae
Megasporaceae
Microcaliciaceae
Ochrolechiaceae
Pertusariaceae
Varicellariaceae

The Pertusariales are an order of fungi in the class Lecanoromycetes, comprising 8 families, 31 genera, and over 600 species,[1] many of which form lichens. This diverse group is characterized by complex taxonomic history and ongoing phylogenetic revisions. Originally circumscribed by lichenologists David L. Hawksworth and Ove Eriksson in 1986, Pertusariales has undergone significant reclassification due to molecular phylogenetics studies. The order includes well-known genera such as Pertusaria and Ochrolechia, as well as families like Megasporaceae and Icmadophilaceae.

Pertusariales species exhibit a wide range of morphological features and ecological roles, from non-lichenized fungi to various forms of lichen symbioses. The order's taxonomy has been subject to considerable debate and revision, with recent research leading to the establishment of new orders and the reassignment of some taxa. This ongoing refinement reflects efforts to more accurately represent evolutionary relationships within the group. Conservation concerns exist for some Pertusariales species, with Lepra andersoniae listed as endangered on the IUCN Red List due to its limited range and specific habitat requirements in the Appalachian Mountains.

Systematics[edit]

The order was formally circumscribed by the lichenologists David L. Hawksworth and Ove Eriksson.[2]

The order Pertusariales, within the class Lecanoromycetes of the Ascomycota, has a complex taxonomic history marked by ongoing revisions and debates. Historically, the order encompassed a diverse group of lichen-forming fungi, including the well-known genus Pertusaria. This grouping was primarily based on morphological characteristics. However, recent molecular phylogenetics analyses have challenged traditional classifications, leading to significant changes. For example, Agyrium rufum, once thought to relate to the Trapeliaceae family within Agyriales, was found to be more closely associated with Pertusaria, justifying the merge of Agyriales into Pertusariales. Yet, this merger sparked controversy over which name should prevail due to taxonomic priorities not extending beyond the family rank in fungal nomenclature.[3]

The revision of Pertusariales was further complicated by the identification and establishment of new orders. Researchers at the New York Botanical Garden proposed the creation of Sarrameanales and Trapeliales to accommodate distinct groups of fungi previously misplaced within Agyriales. These efforts align with modern taxonomic practices aiming to reflect evolutionary relationships more accurately. Consequently, the Trapeliaceae, previously associated with Agyriales, was reassigned to the newly established order Trapeliales based on strong molecular evidence distinguishing it from the Pertusariales. This realignment was part of a broader effort to update the lichen herbarium's taxonomic framework to a phylogenetic system reflecting current understanding.[3]

Furthermore, within the Pertusariales, the inclusion and relationships of various genera and families have been subjects of detailed study. Molecular data have supported the separation of certain genera, leading to clearer distinctions between closely related groups. The order now comprises several families, including Pertusariaceae, which houses the type genus Pertusaria.[3]

Classification[edit]

The classification and detailed breakdown of the order Pertusariales, particularly its division into various genera and families, have been subjects of ongoing debate and reevaluation over many years. Questions have arisen regarding the inclusion of the families Coccotremataceae and Megasporaceae, and the genus Loxosporopsis, as their characteristics partly align with those traditionally associated with Pertusariales but also show notable differences. For instance, Coccotremataceae shares morphological and chemical features with Pertusariaceae yet differs in aspects such as the development of the ascoma, the presence of periphyses, and the type of ascus, alongside the absence or presence of cephalodia. Conversely, molecular evidence has both challenged and supported the inclusion of these taxa within Pertusariales.[4]

Megaspora verrucosa

The genus Megasporaceae, established for the species Megaspora verrucosa, initially placed within Pertusariales, has exhibited close molecular ties to Aspicilia, challenging its previous classification. Meanwhile, Loxosporopsis, described without definitive familial placement within Pertusariales, has molecular ties suggesting a close relationship with Pertusaria s.str., despite differing in septate ascospore formation, chemical makeup, and ascoma development aspects. These examples illustrate the ongoing redefinitions within Pertusariales based on a combination of morphological and molecular analyses.[4]

Furthermore, the separation between the central Pertusariaceae genera, Ochrolechia and Pertusaria, remains ambiguous, highlighted by the existence of several taxa with intermediate traits and the high variability in their characteristics. This has led to frequent reclassifications among these genera. Molecular studies have exposed Pertusaria as polyphyletic, breaking into distinct monophyletic clusters, thereby challenging the traditional monophyletic view of Pertusariaceae. Although subsequent studies have suggested potential monophyly of Pertusariaceae, these findings have lacked definitive support, complicating the taxonomic understanding of Pertusariales and necessitating further research to clarify these complex phylogenetic relationships.[4]

Families and genera[edit]

The order Pertusariales comprises a diverse array of fungi, organized into several distinct families. These families encompass a wide range of morphological and ecological characteristics, from non-lichenized fungi to various forms of lichen symbioses. In 2006, the order was estimated to contain 450–770 species and "two or three families".[4] As of July 2024, according to Species Fungorum in the Catalogue of Life, the order has expanded to include 9 families, 34 genera, and 881 species.[5] This significant increase in recognized taxa reflects ongoing revisions based on new molecular and morphological data.

Agyrium rufum
This family consists of non-lichenized fungi. They produce small, round, sessile fruiting bodies called apothecia. Their asci (spore-containing structures) are club-shaped and contain eight colourless, ellipsoid to nearly spherical spores. These fungi are typically found on wood and are distributed worldwide, particularly in temperate regions.[7]
Agyrium – 3 spp.
Miltidea – 1 sp.
Members of this family are lichenized fungi, forming symbiotic relationships with both green algae and cyanobacteria. Their thalli (fungal bodies) can be crustose, foliose, or fruticose. They produce perithecioid ascomata within wart-like structures. The family is characterized by thick-walled, colourless spores and the presence of certain chemical compounds like depsidones and depsides. They grow on bark, rocks, and soil, with a distribution centered in temperate areas of the Southern Hemisphere.[7]
Coccotrema – 16 spp.
Gyalectaria – 3 spp.
Parasiphula – 7 spp.
Members of Icmadophilaceae: Dibaeis baeomyces (left) and Icmadophila ericetorum
This family comprises lichenized fungi that form symbiotic relationships with green algae. Their thalli range from crustose to fruticose. They produce distinctive fruiting bodies that are often stalked. Their asci are thin-walled and contain eight colourless spores that can be non-septate or have one septum. These lichens typically contain gyrophoric acid and are found on bark, rocks, and soil, particularly in temperate mountainous regions worldwide.[7]
Dibaeis – ca. 14 spp.
Endocena – 2 spp.
Icmadophila – 4 spp.
Knightiellastrum – 1 spp.
Pseudobaeomyces – 1 sp.
Siphula – 26 spp.
Siphulella – 1 sp.
Siphulopsis – 1 sp.
Thamnolia – 6 spp.
Members of Megasporaceae: clockwise from upper left: Aspicilia americana, Circinaria contorta; Lobothallia praeradiosa; and Aspicilia cyanescens
Members of the Megasporaceae are lichenized fungi with thalli ranging from crustose to foliose. They form symbiotic relationships with green algae. Their fruiting bodies are typically immersed in the thallus. The family is characterized by thin-walled asci containing non-septate, ellipsoid spores. They produce various secondary metabolites including aliphatic acids and depsidones. These lichens are often found growing on soil, plant litter, or bryophytes in temperate regions.[7]
Aspicilia – about 200 spp.
Aspiciliella – 4 spp.
Atrostelia[11] – 1 sp.
Circinaria – ca. 40 spp.
Lobothallia – 12 spp.
Megaspora – 4 spp.
Oxneriaria – 16 spp.
Sagedia – ca. 30 spp.
Teuvoa – 5 spp.
This small family consists of non-lichenized or lichenicolous fungi (fungi that grow on lichens). They produce distinctive fruiting bodies called mazaedia (a powdery mass of ascospores and paraphyses), which can be sessile or stalked. Their spores are needle-shaped and colourless. The family is characterized by ellipsoid asci and small, round to ellipsoid conidia. These fungi are typically found growing on bark, wood, or other lichens.[7]
Microcalicium – 4 spp.
Ochrolechia africana
The family Ochrolechiaceae consists of a single genus of crustose lichens that partner with green algae. They produce disc-shaped fruiting bodies (apothecia) with a distinctive structure. Their asci contain large, colourless, non-septate spores. These lichens are known for producing various chemical compounds including depsides, depsidones, and lichexanthone. They can be found growing on bark, rocks, and soil.[7]
Ochrolechia – 60 spp.
This family of lichenized fungi forms crustose thalli in symbiosis with green algae. Their fruiting bodies can be either perithecioid or apothecioid. They are characterized by large, often thick-walled spores, typically produced in small numbers per ascus. The family is known for its diverse secondary metabolites, including chloroatranorin and various acids. These lichens grow on bark, rocks, and soil.[7] Genus Lepra was resurrected in 2017 to accommodate the former Variolaria-group of Pertusaria.[14]
Lepra – 94 spp.
Loxosporopsis – 1 sp.
Pertusariaabout 400 spp.
Thamnochrolechia – 1 sp.
Varicellaria rhodocarpa
This family contains a single genus, Varicellaria, many members of which were transferred from Pertusaria in 2012.[17] Members of this family are crustose lichens that form symbiotic relationships with green algae of the genus Trebouxia. They produce disc-like fruiting bodies (apothecia) and are characterized by a non-amyloid hymenial gel, strongly amyloid asci containing one or two spores, and large, thick-walled, hyaline ascospores with one or two cells. The family was formally established in 2018 after some nomenclatural challenges. Varicellariaceae species have a cosmopolitan distribution and can be found growing on various substrates worldwide.[15]
Varicellaria – 8 spp.

Conservation[edit]

Three Pertusariales species have been assessed for the IUCN global Red List of Threatened Species. One species of particular conservation concern is Lepra andersoniae, which is narrowly endemic to the Appalachian Mountains in the United States and is listed as endangered on the IUCN Red List. It has a limited range, with an extent of occurrence of only 4,027 km² and an area of occupancy of 16 km². The species is known from just three subpopulations across fewer than 10 sites, with an estimated total of 340–570 mature individuals. L. andersoniae faces threats from recreational activities, climate change, and potential habitat loss. It is restricted to sheltered and vertical faces of high-elevation rock outcrops and talus slopes in spruce-fir forests, making it particularly vulnerable to environmental changes. Conservation efforts for this species include monitoring of extant subpopulations, detailed habitat surveys, and the need for a species-specific management plan.[18]

Two other Pertusariales species have been assessed for the IUCN Red List. Pertusaria rhodostoma, known only from a single historical collection in Colombia, is listed as Data Deficient due to a lack of current information on its population, habitat, and potential threats.[19] In contrast, Lepra acroscyphoides, found in the páramo of Colombia, is listed as a least-concern species. While it faces potential threats from agriculture and grazing, its high-elevation habitat in páramo ecosystems provides some natural protection.[20]

References[edit]

  1. ^ Wijayawardene, Nalin; Hyde, Kevin; Al-Ani, Laith Khalil Tawfeeq; Somayeh, Dolatabadi; Stadler, Marc; Haelewaters, Danny; et al. (2020). "Outline of Fungi and fungus-like taxa". Mycosphere. 11: 1060–1456. doi:10.5943/mycosphere/11/1/8.
  2. ^ Eriksson, O.E.; Hawksworth, D.L. (1986). "Outline of the ascomycetes - 1986". Systema Ascomycetum. 5: 185–324.
  3. ^ a b c Hodkinson, Brendan P.; Lendemer, James C. (2011). "The orders of Ostropomycetidae (Lecanoromycetes, Ascomycota): recognition of Sarrameanales and Trapeliales with a request to retain Pertusariales over Agyriales" (PDF). Phytologia. 93 (3): 407–412.
  4. ^ a b c d e Schmitt, Imke; Yamamoto, Yoshikazu; Lumbsch, H. Thorsten (2006). "Phylogeny of Pertusariales (Ascomycotina): resurrection of Ochrolechiaceae and new circumscription of Megasporaceae". Journal of the Hattori Botanical Laboratory. 100: 753–764.
  5. ^ Species Fungorum. "Pertusariales". Catalog of Life. Retrieved 9 July 2024.
  6. ^ Corda, A.C.J. (1838). Icones fungorum hucusque cognitorum [Images of Known Fungi] (in Latin). Vol. 2. p. 36.
  7. ^ a b c d e f g Jaklitsch, Walter; Baral, Hans-Otto; Lücking, Robert; Lumbsch, H. Thorsten (2016). Frey, Wolfgang (ed.). Syllabus of Plant Families: Adolf Engler's Syllabus der Pflanzenfamilien. Vol. 1/2 (13 ed.). Berlin Stuttgart: Gebr. Borntraeger Verlagsbuchhandlung, Borntraeger Science Publishers. pp. 146–149. ISBN 978-3-443-01089-8. OCLC 429208213.
  8. ^ David, J.C.; Hawksworth, D.L. (1991). "Validation of six family names of lichenized ascomycetes". Systema Ascomycetum. 10: 13–18.
  9. ^ Rambold, G.; Triebel, D.; Hertel, H. (1993). "Icmadophilaceae, a new family in the Leotiales". Phytochemistry and Chemotaxonomy of Lichenized Ascomycetes – A Festschrift in Honour of Siegfried Huneck. Bibliotheca Lichenologica. Vol. 53. Berlin/Stuttgart: J. Cramer. pp. 217–240.
  10. ^ Lumbsch, T.H.; Feige, G.B.; Schmitz, K.E. (1994). "Systematic studies in the Pertusariales. I: Megasporaceae, a new family of lichenized ascomycetes". Hattori Shokubutsu Kenkyujo Hokoku. 75: 295–304.
  11. ^ Paukov, Alexander G.; Davydov, Evgeny A.; Yakovchenko, Lidia; Ren, Qiang; Sohrabi, Mohammad (7 December 2023), Atrostelia — a new genus in Megasporaceae (Pertusariales, lichenized Ascomycota), doi:10.21203/rs.3.rs-3687993/v1
  12. ^ Tibell, Leif (1984). A Reappraisal of the Taxonomy of Caliciales. Beihefte zur Nova Hedwigia. Vol. 79. J. Cramer. p. 701.
  13. ^ Körber, G.W. (1855). Systema lichenum Germaniae (in German). p. 377.
  14. ^ Wei, X.L.; Schmitt, I.; Hodkinson, B.P.; Flakus, A.; Kukwa, M.; Divakar, P.K.; Kirika, P.M.; Otte, J.; Meiser, A.; Lumbsch, H.T. (2017). "Circumscription of the genus Lepra, a recently resurrected genus to accommodate the "Variolaria"-group of Pertusaria sensu lato (Pertusariales, Ascomycota)". PLOS ONE. 12 (7): e0180284. Bibcode:2017PLoSO..1280284W. doi:10.1371/journal.pone.0180284. PMC 5507398. PMID 28700682.
  15. ^ a b Kraichak, Ekaphan; Huang, Jen-Pan; Nelsen, Matthew; Leavitt, Steven D.; Lumbsch, H. Thorsten (2018). "A revised classification of orders and families in the two major subclasses of Lecanoromycetes (Ascomycota) based on a temporal approach". Botanical Journal of the Linnean Society. 188 (3): 233–249. doi:10.1093/botlinnean/boy060.
  16. ^ Kraichak, Ekaphan; Huang, Jen-Pan; Nelsen, Matthew; Leavitt, Steven D.; Lumbsch, H. Thorsten (2018). "Nomenclatural novelties". Index Fungorum (375): 1. ISSN 2049-2375.
  17. ^ Schmitt, Imke; Otte, Juergen; Parnmen, Sittiporn; Sadowska-Deś, Anna; Luecking, Robert; Lumbsch, Thorsten (2012). "A new circumscription of the genus Varicellaria (Pertusariales, Ascomycota)". MycoKeys. 4: 23–36. doi:10.3897/mycokeys.4.3545.
  18. ^ Lendemer, J. (6 August 2020). "Gladys' Mountain Spikes. Lepra andersoniae". IUCN Red List of Threatened Species. 6 August 2020. Retrieved 9 July 2024.
  19. ^ Simijaca, D.; Moncada, B.; Soto-Medina, E.; Coca, L.F.; Jaramillo, M. (26 November 2019). "Pertusaria rhodostoma". IUCN Red List of Threatened Species. 26 November 2019. Retrieved 9 July 2024.
  20. ^ Moncada, B.; Simijaca, D.; Soto-Medina, E.; Coca, L.F.; Jaramillo, M. (26 November 2019). "Lepra acroscyphoides". IUCN Red List of Threatened Species. 26 November 2019. Retrieved 9 July 2024.