Graphidaceae
Family of fungi From Wikipedia, the free encyclopedia
The Graphidaceae are a family of lichen-forming fungi in the order Graphidales. The family contains nearly a hundred genera and more than 2000 species.[4] Although the family has a cosmopolitan distribution, most Graphidaceae species occur in tropical regions, and typically grow on bark.[5]
Graphidaceae | |
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Graphis desquamescens | |
Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Fungi |
Division: | Ascomycota |
Class: | Lecanoromycetes |
Order: | Graphidales |
Family: | Graphidaceae Dumort. (1822) |
Type genus | |
Graphis Adans. (1763) | |
Subfamilies | |
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Synonyms[1][2][3] | |
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Taxonomy
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Perspective
Graphidaceae was originally proposed by French botanist Barthélemy Charles Joseph Dumortier in 1822 (as "Graphineae"). Graphis, Opegrapha, and Arthonia were included in the new family.[6]
In 2002, German lichenologist Bettina Staiger revised the Graphidaceae family in a monograph, proposing a new classification of genera that was widely accepted until molecular phylogenetic studies led to a further reorganization of the family.[7]
Two subfamilies are recognized in the Graphidaceae:[5]
- Fissurinoideae Rivas Plata, Lücking & Lumbsch (2011)[1]
- Graphidoideae Rivas Plata, Lücking & Lumbsch (2011)[1]
Subfamily Redonographoideae, proposed by Lücking and colleagues in 2013,[8] has since been promoted to familial status (as the monogeneric family Redonographaceae).[9]
Synonymy
The family Thelotremataceae was placed in synonymy with Graphidaceae in 2008, after molecular phylogenetic analysis showed that the families formed several lineages within one strongly supported monophyletic lineage. This study also showed that many genera in Graphidaceae and Thelotremataceae were paraphyletic or polyphyletic.[10] In 2018,[11] Kraichak and colleagues, using a "temporal phylogenetic" approach to identify temporal bands for specific taxonomic ranks, proposed removing Fissurina from the Graphidaceae and instead as placing it as the type genus of Fissurinaceae, a family originally proposed by Brendan P. Hodkinson in 2012.[12] They similarly suggested recognizing Diploschistaceae and Thelotremataceae as independent families. This taxonomic proposal was rejected by Robert Lücking in a critical 2019 review of the temporal method for the classification of lichen-forming fungi, using these specific examples to highlight several drawbacks of this approach. He noted "there is substantial loss of information content in this alternative classification at the second most important rank, the level of family, and such a revised classification is practically meaningless. It makes more sense to apply such essentially phylogenetic classifications, with less information content, to infraranks, such as subfamily or tribe".[3]
Description
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Perspective

The photosynthetic partner (photobiont) of Graphidaceae fungi is typically green algae from the genus Trentepohlia, or very rarely Trebouxia. The lichen thallus is typically crustose, which means it forms a crust-like structure on the substrate it grows on. The form of the ascomata of Graphidaceae are usually apothecioid (cup-shaped), lirellate (narrow, and slit-like) or perithecioid (round or oval-shaped structure and embedded in the substrate), but can be rarely mazaediate (with a powdery mass of ascospores and paraphyses formed by the disintegration of the asci). They are usually zeorine (with both a thalline exciple and a proper exciple), but are sometimes lecideine (without a thallus margin) or lecanorine (surrounded by a pale thalline margin). The hamathecium, which is the hyphae and tissue that between the asci, consists of usually unbranched, sometimes capitate, rarely branched and anastomosing paraphyses. In some lineages, the paraphyses may be apically spinulose (covered with small spines or projections at the tips), and there may be lateral periphysoids in some lineages. The asci are annelasceous, which means they have a ring structure protruding into the lumen and with an apical tholus. They are non-amyloid or amyloid in some lineages, such as in the genus Diorygma. The asci are clavate to oblong or fusiform in shape.[5]
The ascospores of Graphidaceae number primarily 8 per ascus but can often be reduced to 2–4 or 1 per ascus. They are transversely septate to muriform (elongated and divided into multiple compartments by transverse and longitudinal septa), usually ellipsoid to oblong, and often have endospore forming distosepta and lens-shaped to rounded lumina. This particular set of features is known as "graphidoid". The spores can be hyaline (colourless) to (dark) brown, and the endospore is often amyloid. Graphidaceae also have pycnidia for producing conidia, which are non-septate, usually oblong, and hyaline.[5]
Distribution and ecology
The vast majority of Graphidaceae species are restricted to the tropics. Most Graphidaceae species are epiphytic (i.e. they grow only on plants).[8] Forty-two species are known from the Galápagos Islands, where they are among the most diverse of the crustose lichens there.[13] Mexico is thought to be a biodiversity hotspot of undiscovered Graphidaceae species, with about 430 species predicted to occur in tropical regions,[14] compared to less than 200 recorded in the entire country.[15]
Genera
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Perspective
According to the Catalogue of Life, there are 94 genera and more than 2100 species in Graphidaceae.[4] In terms of number of species, Graphidaceae is the second-largest family of lichen-forming fungi, after the Parmeliaceae (2765 species) and ahead of the Verrucariaceae (943 species).[2] The following list gives the genus name, its taxonomic authority, year of publication, and the number of species:







- Acanthothecis Clem. (1909)[16] – 5 spp.
- Acanthotrema Frisch (2006)[17] – 1 sp.
- Aggregatorygma M.Cáceres, Aptroot & Lücking (2014)[18] – 3 spp.
- Allographa Chevall. (1824)[19] – 183 spp.
- Amazonotrema Kalb & Lücking (2009)[20] – 1 sp.
- Ampliotrema Kalb (2006)[21] – 1 sp.
- Anomalographis Kalb (1992) – 2 spp.
- Anomomorpha Nyl. ex Hue (1891) – 8 spp.
- Asteristion Leight. (1870) – 7 spp.[22]
- Astrochapsa Parnmen, Lücking & Lumbsch (2012)[23] – 29 spp.
- Austrotrema I.Medeiros, Lücking & Lumbsch (2017) – 3 spp.[22]
- Borinquenotrema Merc.-Díaz, Lücking & Parnmen (2014)[24] – 1 sp.
- Byssotrema M.Cáceres, Aptroot & Lücking (2014)[18] – 1 sp.
- Carbacanthographis Staiger & Kalb (2002)[7] – 22 spp.
- Chapsa A.Massal. (1860)[25] – 51 spp.
- Chroodiscus (Müll.Arg.) Müll.Arg. (1890) – 17 spp.
- Clandestinotrema Rivas Plata, Lücking & Lumbsch (2012)[1] – 17 spp.
- Compositrema Rivas Plata, Lücking & Lumbsch (2012)[26] – 4 spp.
- Corticorygma M.Cáceres, S.C.Feuerst., Aptroot & Lücking (2014)[18] – 1 sp.
- Creographa A.Massal. (1860)[27] – 1 spp.
- Cruentotrema Rivas Plata, Papong, Lumbsch & Lücking (2012)[1] – 6 spp.
- Crutarndina Parnmen, Lücking & Lumbsch (2012)[23] – 1 sp.
- Cryptoschizotrema Aptroot, Lücking & M.Cáceres (2019)[28] – 2 spp.
- Cyclographina D.D.Awasthi (1979) – 8 spp.
- Diaphorographis A.W.Archer & Kalb (2009)[29] – 2 spp.
- Diorygma Eschw. (1824) – 74 spp.
- Diploschistes Norman (1852)[30] – 25 spp.
- Dyplolabia A.Massal. (1854)[31] – 5 spp.
- Enigmotrema Lücking (2012) – 1 sp.
- Fibrillithecis Frisch (2006)[17] – 15 spp.
- Fissurina Fée (1825)[32] – 117 spp.
- Gintarasia Kraichak, Lücking & Lumbsch (2013)[33] – 7 spp.
- Glaucotrema Rivas Plata & Lumbsch (2012)[34] – 5 spp.
- Glyphis Ach. (1814) – 7 spp.
- Graphina Müll.Arg. (1880) – 25 spp.
- Graphis Adans. (1763) – ca. 275 spp.
- Gyrotrema Frisch (2006)[17] – 6 spp.
- Halegrapha Rivas Plata & Lücking (2011)[35] – 9 spp.
- Heiomasia Nelsen, Lücking & Rivas Plata (2010)[36] – 3 spp.
- Hemithecium Trevis. (1853) – ca. 50 spp.
- Jocatoa R.Miranda (2020)[15] – 1 sp.
- Kalbographa Lücking (2007)[37] – 5 spp.
- Leiorreuma Eschw. (1824) – 18 spp.
- Leptotrema Mont. & Bosch (1856)[38] – 14 spp.
- Leucodecton A.Massal. (1860)[27] – 32 spp.
- Malmographina M.Cáceres, Rivas Plata & Lücking (2011)[39] – 1 sp.
- Mangoldia Lücking, Parnmen & Lumbsch (2012)[40] – 4 spp.
- Medusulina Müll.Arg. (1894)[41]
- Melanotopelia Lumbsch & Mangold (2008)[42] – 4 spp.
- Melanotrema Frisch (2006)[43] – 12 spp.
- Myriochapsa M.Cáceres, Lücking & Lumbsch (2013)[44] – 3 spp.
- Myriotrema Fée (1825) – 76 spp.
- Nadvornikia Tibell (1984)[45] – 5 spp.
- Nitidochapsa Parnmen, Lücking & Lumbsch (2013) – 5 spp.
- Ocellularia G.Mey. (1825)[46] – 343 spp.
- Pallidogramme Staiger, Kalb & Lücking (2008)[47] – 13 spp.
- Paratopeliopsis Merc.-Díaz, Lücking & Parnmen (2014)[24] – 1 sp.
- Phaeographina Müll.Arg. (1882)[48] – 11 spp.
- Phaeographis Müll.Arg. (1882) – ca. 180 spp.
- Phaeographopsis Sipman (1997)[49] – 3 spp.
- Phaeotrema Müll.Arg. (1887)[50] – 19 spp.
- Platygramme Fée (1874)[51] – 30 spp.
- Platythecium Staiger (2002)[7] – 27 spp.
- Pliariona A.Massal. (1860)[27] – 1 sp.
- Polistroma Clemente ex Ach. (1814)[52] – 1 sp.
- Pseudochapsa Parnmen, Lücking & Lumbsch (2012)[23] – 18 spp.
- Pseudoramonia Kantvilas & Vězda (2000)[53] – 4 spp.
- Pseudotopeliopsis Parnmen, Lücking & Lumbsch (2012)[23] – 4 spp.
- Pycnotrema Rivas Plata & Lücking (2012)[54] – 2 spp.
- Redingeria Frisch (2006)[17] – 8 spp.
- Reimnitzia Kalb (2001)[55] – 1 sp.
- Rhabdodiscus Vain. (1921)[56] – 36 spp.
- Sanguinotrema Lücking (2015)[57] – 1 sp.
- Sarcographa Fée (1825) – 37 spp.
- Sarcographina Müll.Arg. (1887) – 6 spp.
- Schistophoron Stirt. (1876) – 5 spp.
- Schistostoma Stirt. (1879) – 1 sp.
- Schizotrema Mangold & Lumbsch (2009)[58] – 7 spp.
- Stegobolus Mont. (1845) – 16 spp.
- Thalloloma Trevis. (1853)[59] – 20 spp.
- Thecaria Fée (1825) – 4 spp.
- Thecographa A.Massal. (1860) – 3 spp.
- Thelotrema Ach. (1803) – 165 spp.
- Topeliopsis Kantvilas & Vězda (2000)[53] – 20 spp.
- Tremotylium Nyl. (1865)[60] – 4 spp.
- Wirthiotrema Rivas Plata, Kalb, Frisch & Lumbsch (2010)[61] – 5 spp.
- Xalocoa Kraichak, Lücking & Lumbsch (2013)[33]– 1 sp.
References
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