identifier	taxonID	type	CVterm	format	language	title	description	additionalInformationURL	UsageTerms	rights	Owner	contributor	creator	bibliographicCitation
0397B65BFFBA5C39FF75FCC751C277B9.text	0397B65BFFBA5C39FF75FCC751C277B9.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cruentotrema Rivas Plata, Papong, Lumbsch & Lücking 2012	<div><p>Key to the species of Cruentotrema, Dyplolabia, and Enigmotrema</p> <p>Distribution data are based on Lücking et al. (2014), with additions given in this paper.</p> <p>1. Ascomata with (dark) red, K+ green pigment (isohypocrelline)..................................................................................................... 2.</p> <p>- Ascomata without pigment.............................................................................................................................................................. 6.</p> <p>2. Ascomata remaining closed, perithecioid (Fig. 2A; ascospores 3-septate; Neotropics (Costa Rica).............................................................................................................................................................. Enigmotrema rubrum Lücking in Sipman et al. (2012: 66)</p> <p>- Ascomata opening by rupturing into erect to recurved lobules; ascospores 3-septate to submuriform (Cruentotrema p.p.)......... 3.</p> <p>3. Ascospores 3-septate; ascomata angular rounded to lirelliform...................................................................................................... 4.</p> <p>- Ascospores submuriform; ascomata angular-rounded.................................................................................................................... 5.</p> <p>4. Ascomata lirelliform (Fig. 2B–D); eastern Paleotropics (Thailand)................................... Cruentotrema lirelliforme (see below)</p> <p>- Ascomata angular-rounded (Fig. 2E–F); eastern Paleotropics (Thailand).......................................................................................................................................... Cruentotrema thailandicum Rivas Plata, Papong &amp; Lumbsch in Rivas Plata et al. (2012a: 119)</p> <p>5. Ascospores 15–20(–23) × 7–10 μm; disc bright red to pinkish (Fig. 3A–D); eastern Paleotropics (Thailand, Australia, New Caledonia).................................................................................................................................... Cruentotrema puniceum (see below)</p> <p>- Ascospores 20–30 × 8–14 μm; disc (dark) red (Fig. 3E–F); Neotropics (Central and South America) and eastern Paleotropics (Australia).................. Cruentotrema cruentatum (Mont.) Rivas Plata, Lumbsch &amp; Lücking in Rivas Plata et al. (2012a: 119)</p> <p>6. Ascomata immersed-erumpent, opening by rupturing into erect to recurved thalline lobules which often fall off, with brownishgrey disc and thin carbonization (Cruentotrema p.p.)..................................................................................................................... 7.</p> <p>- Ascomata prominent to sessile, lirelliform with distinct, well-carbonized labia with thick, (yellowish) white, C+ red cover, if erumpent and with irregular lobules, then also well-carbonized and lobules with thick, white, C+ red cover (Dyplolabia)......... 8.</p> <p>7. Ascospores 3-septate (Fig. 4A–B); Neotropics (Brazil)..................................................................................................................................................................................... Cruentotrema amazonum M. Cáceres, Aptroot &amp; Lücking in Cáceres et al. (2014: 92)</p> <p>- Ascospores submuriform (Fig. 4C–F); eastern Paleotropics (India, Thailand, Australia)................................................................................................. Cruentotrema kurandense (Mangold) Rivas Plata, Lumbsch &amp; Lücking in Rivas Plata et al. (2012a: 119)</p> <p>8. Ascospores 3-septate; ascomata lirelliform..................................................................................................................................... 9.</p> <p>- Ascospores (sub-)muriform); ascomata angular-rounded or lirelliform....................................................................................... 10.</p> <p>9. Lirellae short, 1–3(–5) mm long, with white cover; ascospores 16–22 × 7–10 μm (Fig. 5A–C); pantropical............................................................................................................................................ Dyplolabia afzelii (Ach.) A. Massal. in Massalongo (1854: 6)</p> <p>- Lirellae very long, 10–30 mm, with yellowish white cover; ascospores 14–17 × 5–7 μm (Fig. 5D–F); eastern Paleotropics (Sri Lanka, Thailand)....................................................................................................................... Dyplolabia ochrocheila (see below)</p> <p>10. Ascomata angular-rounded, often with irregular, white pseudocolumella; ascospores 25–30 × 15–20 μm (Fig. 6A); eastern Paleotropics (Philippines).................................................................................................................. Dyplolabia dalywaiana (see below)</p> <p>- Ascomata lirelliform...................................................................................................................................................................... 11.</p> <p>11. Ascospores 19–27 × 10–14 μm (Fig. 6B–D); pantropical................................................................................................................................................................................................. Dyplolabia oryzoides (Leight.) Kalb &amp; Staiger in Kalb &amp; Staiger (2000: 418)</p> <p>- Ascospores 16–19 × 8–9 μm (Fig. 6E–F); eastern Paleotropics (Thailand)................................................................................................................................................................................................... Dyplolabia chumphonensis J. Kalb &amp; K. Kalb (see below)</p> </div>	https://treatment.plazi.org/id/0397B65BFFBA5C39FF75FCC751C277B9	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Polyiam, Jutarat Kalb Wetchasart;Plata, Eimy Rivas;Bawingan, Paulina A.;Kalb, Klaus;Lücking, Robert	Polyiam, Jutarat Kalb Wetchasart, Plata, Eimy Rivas, Bawingan, Paulina A., Kalb, Klaus, Lücking, Robert (2016): ‘ Missing links’ alive? Novel taxa represent morphological transitions between distinctive phenotypes among extant Graphidaceae (lichenized Ascomycota: Ostropales). Phytotaxa 268 (2): 110-122, DOI: 10.11646/phytotaxa.268.2.2, URL: http://dx.doi.org/10.11646/phytotaxa.268.2.2
0397B65BFFBD5C3EFF75F97E56DB77FE.text	0397B65BFFBD5C3EFF75F97E56DB77FE.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cruentotrema kurandense (Mangold) Rivas Plata, Lumbsch & Lucking	<div><p>Cruentotrema kurandense (Mangold) Rivas Plata, Lumbsch &amp; Lücking</p> <p>Remarks:— Cruentotrema kurandense is newly reported for Thailand.</p> <p>Specimens examined: ― THAILAND. Nakhon Ratchasima: Khao Yai National Park, Pha Trom Jai, Khao Khieo; 14 December 2000, S. Jariangprasert 1352 (MJU). Phang-gna: Takua Pa District, Tambon Khuekkhak, Samnaksong Bandokdang, at Phetkasem Road (Road Nr. 4), a few km S of Bangsak Village, on deciduous trees in a secondary forest; 08°45’35’’ N, 98°19’13’’ E, 45 m; 8 June 2015, J. Sutjaritturakan &amp; K. Kalb (herb. K. Kalb 41184). Ranong: Area of Ban Heownumsai along side road from Phetkasem road (Road No. 4) to Ton Petch Waterfall (Rainbow Waterfall), ca. 30 km S of Ranong City, in a palm tree plantation; 09°43’28’’ N, 98°36’52’’ E, 20 m; 6 June 2015, J. Sutjaritturakan &amp; K. Kalb (herb. K. Kalb 41384).</p> </div>	https://treatment.plazi.org/id/0397B65BFFBD5C3EFF75F97E56DB77FE	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Polyiam, Jutarat Kalb Wetchasart;Plata, Eimy Rivas;Bawingan, Paulina A.;Kalb, Klaus;Lücking, Robert	Polyiam, Jutarat Kalb Wetchasart, Plata, Eimy Rivas, Bawingan, Paulina A., Kalb, Klaus, Lücking, Robert (2016): ‘ Missing links’ alive? Novel taxa represent morphological transitions between distinctive phenotypes among extant Graphidaceae (lichenized Ascomycota: Ostropales). Phytotaxa 268 (2): 110-122, DOI: 10.11646/phytotaxa.268.2.2, URL: http://dx.doi.org/10.11646/phytotaxa.268.2.2
0397B65BFFBC5C3FFF75FF6F515174B8.text	0397B65BFFBC5C3FFF75FF6F515174B8.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cruentotrema lirelliforme J. Kalb, Polyiam & K. Kalb 2016	<div><p>Cruentotrema lirelliforme J. Kalb, Polyiam &amp; K. Kalb, sp. nov. (Fig. 2B–D)</p> <p>MycoBank MB817435</p> <p>Differing from Cruentotrema thailandicum in the lirelliform ascomata.</p> <p>Type: ― THAILAND. Nakon Ratchasima: Khao Yai National Park, about 100 m on road from training center to Haoo Suwat waterfall; 04º44’ N, 73º50’ W, 3600 m; tropical rain forest, on bark; 20 October 2002, W. Polyiam 21520 (holotype RAMK).</p> <p>Thallus corticolous, epiperidermal, grey-olive, smooth to uneven, with dense, prosoplectenchymatous cortex; photobiont layer with scattered clusters of calcium oxalate crystals. Apothecia erumpent, angular to elongate-lirellate, 1–3(–5) mm long and 0.7–1 mm broad; disc immersed, thinly white-pruinose but hidden by a splitting thallus layer that exposes a deep red-pigmented medulla (easily mistaken for representing the disc); margin formed by the outer portions of the thallus layer, erect to fissured, partly flaking off, grey-olive, inner parts red-pruinose. Excipulum prosoplectenchymatous, dark brown or upper half carbonized. Periphysoids absent. Columella absent. Hymenium 90–100 μm high; paraphyses unbranched. Ascospores 8/ascus, 3-septate, 20–30 × 7–10 μm, ellipsoid, with thick septa and diamond-shaped lumina (Astrothelium - type), colorless, I– (non-amyloid).</p> <p>Secondary chemistry: —Medulla of apothecial margin with dark red, K+ yellowish green pigment (isohypocrelline).</p> <p>Etymology: ―The epithet refers to the peculiar morphology of the ascomata.</p> <p>Distribution and ecology: ― Thailand; thus far only known from the type locality, growing on bark of trees in the rain forest understory.</p> <p>Remarks: ―This new species has the typical features of Cruentotrema species, i.e. the red medullary pigment in the ascomata, the ascomata opening by rupturing into irregular lobules, and the I-negative, Astrothelium - type ascospores, but differs clearly in the lirelliform ascomata. It provides a morphological transition towards Dyplolabia, but is also reminescent of certain species of Acanthothecis with partially exposed, reddish disc, such as A. mirabilis Staiger &amp; Kalb (1999: 107), A. rosea (Vain.) Staiger &amp; Kalb in Staiger (2002: 81), and A. sanguinoloba (Redinger) Staiger &amp; Kalb (1999: 110), as well as Fissurina species with partially exposed disc and lobulate margins, although red pigments are absent in that genus (Staiger 2002). Acanthothecis is phylogenetically unrelated and differs by the spinulose paraphyses and the thin ascospore septa, as well as the lack of carbonization. Fissurina, on the other hand, is a polyphyletic agglomerate, with several lineages more closely related to Cruentotrema and Dyplolabia.</p> </div>	https://treatment.plazi.org/id/0397B65BFFBC5C3FFF75FF6F515174B8	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Polyiam, Jutarat Kalb Wetchasart;Plata, Eimy Rivas;Bawingan, Paulina A.;Kalb, Klaus;Lücking, Robert	Polyiam, Jutarat Kalb Wetchasart, Plata, Eimy Rivas, Bawingan, Paulina A., Kalb, Klaus, Lücking, Robert (2016): ‘ Missing links’ alive? Novel taxa represent morphological transitions between distinctive phenotypes among extant Graphidaceae (lichenized Ascomycota: Ostropales). Phytotaxa 268 (2): 110-122, DOI: 10.11646/phytotaxa.268.2.2, URL: http://dx.doi.org/10.11646/phytotaxa.268.2.2
0397B65BFFBC5C3FFF75FB2750017624.text	0397B65BFFBC5C3FFF75FB2750017624.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Cruentotrema puniceum (Mull. Arg.) J. Kalb & K. Kalb 2016	<div><p>Cruentotrema puniceum (Müll. Arg.) J. Kalb &amp; K. Kalb, comb. nov. (Fig. 3A–D)</p> <p>MycoBank MB817483</p> <p>Basionym: ― Arthothelium puniceum Müll. Arg., Hedwigia 32: 133 (1893); Thelotrema puniceum (Müll. Arg.) Makhija &amp; Patw., Tropical Bryology 10: 213 (1995); Chapsa punicea (Müll. Arg.) Cáceres &amp; Lücking, Libri Botanici 22: 54 (2007).</p> <p>Thelotrema rhododiscum Homchant. &amp; Coppins, The Lichenologist 34: 135 (2002).</p> <p>Remarks: ―This species was considered a synonym of Cruentotrema cruentatum, but differs in the smaller and relatively narrower ascospores and the bright red to pinkish disc of the ascomata. Thelotrema rhododiscum is a synonym. The species appears to be the eastern paleotropical vicariant of C. cruentatum.</p> </div>	https://treatment.plazi.org/id/0397B65BFFBC5C3FFF75FB2750017624	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Polyiam, Jutarat Kalb Wetchasart;Plata, Eimy Rivas;Bawingan, Paulina A.;Kalb, Klaus;Lücking, Robert	Polyiam, Jutarat Kalb Wetchasart, Plata, Eimy Rivas, Bawingan, Paulina A., Kalb, Klaus, Lücking, Robert (2016): ‘ Missing links’ alive? Novel taxa represent morphological transitions between distinctive phenotypes among extant Graphidaceae (lichenized Ascomycota: Ostropales). Phytotaxa 268 (2): 110-122, DOI: 10.11646/phytotaxa.268.2.2, URL: http://dx.doi.org/10.11646/phytotaxa.268.2.2
0397B65BFFBC5C3DFF75F974516D76E2.text	0397B65BFFBC5C3DFF75F974516D76E2.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dyplolabia chumphonensis J. Kalb & K. Kalb 2016	<div><p>Dyplolabia chumphonensis J. Kalb &amp; K. Kalb, sp. nov. (Fig. 6E–F)</p> <p>MycoBank MB817436</p> <p>Differing from Dyplolabia oryzoides by smaller ascospores.</p> <p>Type: — THAILAND. Chumphon province: Tasae district, Tambon Tha Sae; area of 72 nd Anniversary Queen Sirikit Park; 10°43’24’’ N, 99°15’43’’ E, 100 m; on a ± free standing deciduous tree; 19 March 2011, J. Sutjaritturakan 3606 (holotype RAMK 027820).</p> <p>Thallus corticolous, epiperidermal, yellow-olive, smooth to uneven, with dense, prosoplectenchymatous cortex; photobiont layer without or with very rare scattered clusters of calcium oxalate crystals.Apothecia erumpent, elongate-lirellate, 1–4 mm long and 0.5–0.75 mm broad, straight or curved, very rarely branched; disc immersed, thickly white-pruinose, fully covered by margin; proper margin distinct, thick, erect, black but with a very thick, white cover; thalline margin absent. Excipulum apically and laterally carbonized, jet-black, without discernable structure. Periphysoids absent but hymenium laterally with a broad zone of widely spaced, anastomosing paraphyses embedded in a gelatinous matrix. Pseudocolumella absent. Hymenium 75–110 μm high; paraphyses unbranched except for lateral areas as described above.Ascospores 4–6 (–8)/ascus, uniseriate, submuriform with 3–5 transverse and 0–1 longitudinal septa per segment, 16–19 × 8–9 μm, oval, with mostly thick septa (rarely thin septa) and diamond-shaped lumina (Astrothelium - type), colorless, I– (non-amyloid).</p> <p>Secondary chemistry: —White cover of ascoma margin C+ red (lecanoric acid).</p> <p>Etymology: ―This new species is named after the Thai province where it was collected.</p> <p>Distribution and ecology: ― Thailand; thus far only known a single collection from the type locality, growing on bark of a deciduous tree in a park.</p> <p>Remarks: ― Dyplolabia chumphonensis is very similar to D. afzelii and D. oryzoides. The first one very rarely has one longitudinal septum per spore (Kalb &amp; Staiger, 2000), but is usually separated by only 4-locular ascospores without a longitudinal septum. The spores of D. oryzoides are considerably larger, 19–27 × 10–14 μm.</p> </div>	https://treatment.plazi.org/id/0397B65BFFBC5C3DFF75F974516D76E2	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Polyiam, Jutarat Kalb Wetchasart;Plata, Eimy Rivas;Bawingan, Paulina A.;Kalb, Klaus;Lücking, Robert	Polyiam, Jutarat Kalb Wetchasart, Plata, Eimy Rivas, Bawingan, Paulina A., Kalb, Klaus, Lücking, Robert (2016): ‘ Missing links’ alive? Novel taxa represent morphological transitions between distinctive phenotypes among extant Graphidaceae (lichenized Ascomycota: Ostropales). Phytotaxa 268 (2): 110-122, DOI: 10.11646/phytotaxa.268.2.2, URL: http://dx.doi.org/10.11646/phytotaxa.268.2.2
0397B65BFFBE5C30FF75F8B255847135.text	0397B65BFFBE5C30FF75F8B255847135.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dyplolabia dalywaiana Rivas Plata, Bawingan & Lucking 2016	<div><p>Dyplolabia dalywaiana Rivas Plata, Bawingan &amp; Lücking, sp. nov. (Fig. 6A)</p> <p>MycoBank MB817437</p> <p>Differing from other Dyplolabia species in the angular, erumpent asomata with broadly exposed disc and irregular pseudocolumella. Type: ― PHILIPPINES. Nueva Vizcaya (Luzon): Mt. Palali, near Solano; 16° 26’ N, 121° 13’ E, 1000 m; montane rain forest; on lower trunk in semi-exposed situation; March 2007, Rivas Plata &amp; Lücking 1194D (holotype F).</p> <p>Thallus corticolous, epiperidermal, yellow-olive, smooth to uneven, with dense, prosoplectenchymatous cortex; photobiont layer with scattered clusters of calcium oxalate crystals.Apothecia erumpent, angular, 1–1.5 mm diam.; disc immersed, thickly white-pruinose, partly covered by margin; proper margin distinct, thick, erect, fissured, black but with a very thick, white cover; thalline margin absent. Excipulum laterally carbonized, jet-black, without discernable structure. Periphysoids absent but hymenium laterally with a broad zone of widely spaced, anastomosing paraphyses embedded in a gelatinous matrix. Pseudocolumella sometimes present, plug-shaped. Hymenium 170–200 μm high; paraphyses unbranched except for lateral areas as described above. Ascospores 8/ascus, uniseriate, muriform with (3–)5 transverse and 1–3 longitudinal septa per segment, 25–30 × 15–20 μm, broadly oval to subglobose, with thick septa and diamond-shaped lumina (Astrothelium - type), colorless, I– (non-amyloid).</p> <p>Secondary chemistry: —White cover of ascoma margin C+ red (lecanoric acid).</p> <p>Etymology: ―This new species is dedicated to the legacy of Charles R. Darwin and his contemporaneous colleagues, Charles Lyell and Afred Russell Wallace, bringing forward the theory of evolution by natural selection and popularizing the use of the term ‘missing link’.</p> <p>Distribution and ecology: ― Philippines; thus far only known a single collection from the type locality, Mt. Palali, growing on bark of trees in the montane rain forest understory.</p> <p>Remarks: ― Dyplolabia dalywaiana is a very peculiar species. It was first believed to represent a member of Ocellularia s.lat., similar to the genera Rhabdodiscus and Stegobolus because of the presence of an irregular columella. The close phylogenetic relationship with D. afzelii initially came as a surprise, but closer examination of the material then revealed that this species shares important characters with the latter, namely the ascoma margin forming a carbonized base with a thick white, C+ red cover containing lecanoric acid, and the I-negative, astrothelioid ascospores. Morphologically, D. dalywaiana is transitional between Dyplolabia and Cruentotrema and hence provides an important taxon to explain the close relationship between both genera: its ascomata have a partially exposed disc and lobulate margins, as in Cruentotrema, whereas the internal anatomy and the thick white cover with lecanoric acid place the species in Dyplolabia.</p> </div>	https://treatment.plazi.org/id/0397B65BFFBE5C30FF75F8B255847135	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Polyiam, Jutarat Kalb Wetchasart;Plata, Eimy Rivas;Bawingan, Paulina A.;Kalb, Klaus;Lücking, Robert	Polyiam, Jutarat Kalb Wetchasart, Plata, Eimy Rivas, Bawingan, Paulina A., Kalb, Klaus, Lücking, Robert (2016): ‘ Missing links’ alive? Novel taxa represent morphological transitions between distinctive phenotypes among extant Graphidaceae (lichenized Ascomycota: Ostropales). Phytotaxa 268 (2): 110-122, DOI: 10.11646/phytotaxa.268.2.2, URL: http://dx.doi.org/10.11646/phytotaxa.268.2.2
0397B65BFFB35C30FF75FE87517272E9.text	0397B65BFFB35C30FF75FE87517272E9.taxon	http://purl.org/dc/dcmitype/Text	http://rs.tdwg.org/ontology/voc/SPMInfoItems#GeneralDescription	text/html	en	Dyplolabia ochrocheila (Vain.) Rivas Plata & Lucking 2016	<div><p>Dyplolabia ochrocheila (Vain.) Rivas Plata &amp; Lücking, comb. nov. (Fig. 5D–F)</p> <p>MycoBank MB817439</p> <p>Basionym: ― Graphis ochrocheila Vain., Hedwigia 46: 178 (1907).</p> <p>Type: ― THAILAND. Trat: Koh Chang Island; 1900, J. Schmidt s.n. (holotype TUR-VAINIO 27535!).</p> <p>Remarks: ―This species was considered a synonym of Dyplolabia afzelii, but differs by the extremely long ascomata and the smaller ascospores, as well as the more yellowish cover of the lirellae (old collections of D. afzelii retain a white cover). Only two collections are known from this taxon so far, from Sri Lanka and Thailand, and this taxon needs further study.</p> <p>Additional specimen examined: ― SRI LANKA. South of the island, s.dat., G. Thwaites 150 (FH).</p></div> 	https://treatment.plazi.org/id/0397B65BFFB35C30FF75FE87517272E9	Public Domain	No known copyright restrictions apply. See Agosti, D., Egloff, W., 2009. Taxonomic information exchange and copyright: the Plazi approach. BMC Research Notes 2009, 2:53 for further explanation.		Plazi	Polyiam, Jutarat Kalb Wetchasart;Plata, Eimy Rivas;Bawingan, Paulina A.;Kalb, Klaus;Lücking, Robert	Polyiam, Jutarat Kalb Wetchasart, Plata, Eimy Rivas, Bawingan, Paulina A., Kalb, Klaus, Lücking, Robert (2016): ‘ Missing links’ alive? Novel taxa represent morphological transitions between distinctive phenotypes among extant Graphidaceae (lichenized Ascomycota: Ostropales). Phytotaxa 268 (2): 110-122, DOI: 10.11646/phytotaxa.268.2.2, URL: http://dx.doi.org/10.11646/phytotaxa.268.2.2
