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Usnea orientalis (Y. Ohmura 7347, TNS). A. Thallus. B. Base of thallus. C. Apothecia. D. Inflated branch. Scales: A ῌ C  ̓̀ 1 mm; D  ̓̀ 0.5 mm. 

Usnea orientalis (Y. Ohmura 7347, TNS). A. Thallus. B. Base of thallus. C. Apothecia. D. Inflated branch. Scales: A ῌ C ̓̀ 1 mm; D ̓̀ 0.5 mm. 

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A key to the 40 taxa in the genus Usnea in Taiwan is presented. Usnea articulata is new to Taiwan. Usnea mutabilis is excluded from the lichen flora of Taiwan. Photographs of diagnostic features are also provided for the species that have not been adequately illustrated previously based on the Asian materials. Orthographical errors were corrected i...

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Context 1
... uniflated; medulla dense; axis thick ῌῌ U. di # racta Vain. (Fig. 12) 13b. Thallus anisotomic-dichotomously branched; branches inflated; medulla loose; axis thin ῌῌῌῌῌῌῌῌῌῌῌ 14 14a. Pseudocyphellae present on branch sur- farce; salazinic acid present ῌῌῌ U. himalayana C.Bab. (Fig. 17) 14b. Pseudocyphellae absent; fumarprotocetraric acid present ῌῌ U. articulata (L.) Ho # m. (Fig. 5) 15a. Apothecia with few or no fibrils along the thalloid exciple ῌῌῌῌῌῌῌῌῌ 16 15b. Apothecia with many fibrils along the thalloid exciple ῌῌῌῌῌῌῌῌῌ 17 16a. Branches uninflated; base of thallus distinctly annulary cracked; barbatic acid present ῌῌῌῌ U. dendritica Stirt. (Fig. 11) 16b. Branches inflated; base of thallus continuous or irregulary cracked; barbatic acid absent ῌῌ U. pseudogatae Asahina (Fig. 26) 17a. Fibrils crisp ῌῌῌ U. masudana Asahina (Fig. 19) 17b. Fibrils straight ῌῌῌῌῌῌῌῌῌῌ 18 18a. Thallus with jet black base; thamnolic acid present ῌ U. florida (L.) F. H. Wigg. (Fig. 13) 18b. Thallus with concolor base; thamnolic acid absent ῌῌῌῌῌῌῌῌῌῌ 19 19a. Fibrils on apothecia broadened at the base ῌῌῌ U. shimadae Asahina (Fig. 28) 19b. Fibrils on apothecia cylindrical at the base ῌῌῌῌῌῌῌῌῌῌῌῌῌ 20 20a. Branches uninflated, matt on the surface; caperatic acid present ῌῌῌῌ U. sinensis Motyka (Fig. 29) 20b. Branches inflated, glossy on the surface; caperatic acid absent ῌῌῌῌῌῌ 21 21a. Apothecia cup-shaped at least when juvenile ῌῌ U. fuscorubens Motyka (Fig. 14) 21b. Apothecia flat through the juvenile to mature stages U. orientalis Motyka (Fig. ...
Context 2
... [Fig. 22] For a description and a synonym, see Ohmura (2001). Chemistry. Usnic, salazinic, and protocetraric ( ῌ ) acids. The distinguishing features of U. orientalis are (1) the erect thallus with anisotomic- dichotomous branching, (2) the inflated branches with glossy surface, (3) the cylindrical papillae on thicker branches, (4) the absence of soralia, (5) the flat apothecia through the juvenile to mature stages, (6) the disc without white rim, (7) the ceratina -type plectenchymatous cortex, and (8) the ...

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... The screening and study of the type material of these 1,200 species is a long and tedious work. Modern accounts of the genus Usnea on the Asian continent were published by Awasthi (1986) for India, Ohmura (2001Ohmura ( , 2012, Ohmura et al. (2010), and Lin (2007) for Japan and Taiwan, Golubkova et al. (1996) for Russia and Ohmura et al. (2017) for the Far East Russia. Zhao et al. (1975) described 12 new species occurring in China. ...
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... Eumitria is characterized by the presence of a tubular central axis (with the exception of U. pectinata with a partially fistulose axis). It has a wide distribution, with taxa occurring in Africa (Swinscow & Krog 1974;Temu et al. 2019), Asia (Ohmura 2001(Ohmura , 2012, Australia (Stevens 1999) and South America (Truong & Clerc 2013). Its morphological circumscription is diffuse since species without a central tubular axis (but with a partially fistulose axis) might cluster together in a molecular phylogeny (within a strongly supported clade) with species having a central tubular axis (Truong et al. 2013a). ...
... More sequenced specimens of U. angulata need to be analyzed to better understand its variability. Regarding the chemistry, although caperatic acid is reported for this species (Ohmura 2012, 2020), we did not find that Figure 2. Molecular phylogeny of Usnea focusing on the species from the Philippines. The phylogeny is based on ITS rDNA sequence data and analyzed using maximum likelihood (RAxML) inference. ...
... Sequenced specimens from Tanzania and São Tomé also have salazinic and norstictic acids (Temu et al. 2019;) but apparently without zeorin. In addition to norstictic acid and zeorin, eumitrins (red pigment present in the medulla) were found in specimens from Japan and Taiwan (Ohmura 2001(Ohmura , 2012. Eumitrins and zeorin were also reported from South American specimens (Truong & Clerc 2013). ...
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... Eumitrioid Usnea has been studied in Africa (Motyka 1936;Dodge 1956;Swinscow & Krog 1974, 1986Krog 1994;Nadel 2016;Temu & al. 2019), Australia (Rogers & Stevens 1988;Stevens 1999), East Asia (Zhao & al. 1982;Ohmura 2001Ohmura , 2012, and South America including the Galapagos (Truong & Clerc 2013). Wei (1991) enumerated about 80 species of Usnea reported in the literature for lichen collections from China before 1989. ...
... Wei (1991) enumerated about 80 species of Usnea reported in the literature for lichen collections from China before 1989. Since then, a series of studies on the diversity and taxonomy of Usnea from China have been carried out (Aptroot & al. 1999(Aptroot & al. , 2002Ohmura 2001Ohmura , 2012Seaward & Aptroot 2005;Zhang & al. 2006;Ohmura & al. 2010;Han & al. 2020). Approximately 90 species of Usnea have now been reported from China, among which seven species are eumitrioid (Zhao & al. 1982;Ohmura 2001Ohmura , 2012Han & al. 2020;Wei 2020). ...
... Since then, a series of studies on the diversity and taxonomy of Usnea from China have been carried out (Aptroot & al. 1999(Aptroot & al. , 2002Ohmura 2001Ohmura , 2012Seaward & Aptroot 2005;Zhang & al. 2006;Ohmura & al. 2010;Han & al. 2020). Approximately 90 species of Usnea have now been reported from China, among which seven species are eumitrioid (Zhao & al. 1982;Ohmura 2001Ohmura , 2012Han & al. 2020;Wei 2020). ...
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Usnea esperantiana is reported as new to Asia. It was collected from Taiwan where it grew on coniferous and broad-leaf trees at elevations between 1716 and 2580 m. The ITS rDNA sequences of Taiwanese and European materials of U. esperantiana form a monophyletic clade within the already reported clade consisting of U. cornuta and the related taxa. Although two distinct clades were formed in the U. esperantiana clade, no morphological and chemical differences were found between them. All Taiwanese specimens contain usnic, salazinic and bourgeanic acids. The description is given based on the Taiwanese specimens.