Abstract:<em>Lewinskya graphiomitria </em>(Müll. Hal. ex Beckett) F. Lara, Garilleti & Goffinet, hitherto considered a New Zealand endemic species, has recently been repeatedly found at different localities in China, thereby representing an intriguing example of a remote intercontinental disjunction among the bryophytes. Herein, the current distribution of this species is reviewed and mapped and its disjunct occurrence in the two widely separated areas is discussed. Maps showing the quantification o… Show more
“…Epiphytic bryophytes are generally willing to occupy the bark of trees both in temperate forests and in more humid tropical areas [ 13 ]. With approximately 850 widely distributed subcosmopolitan species, the family Orthotrichaceae [ 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 ] is one of the main components of the cryptogam epiphytic communities and occurs on tree trunks and branches, and occasionally they are found also in saxicolous habitats. In Central and East Asia, the family is represented by eight genera, namely Leratia , Lewinskya , Macrocoma , Macromitrium , Nyholmiella , Orthotrichum , Ulota, and Zygodon , which can be found in most biomes, from tundra to wet tropical forests.…”
Epiphytes, including vascular and non-vascular, constitute a large part of global plant biodiversity. Distribution of obligatory epiphytic bryophytes results from climate and local habitat conditions. The most important epiphytic bryophytes and at the same time poorly investigated and taxonomically problematic ones belong to the family Orthotrichaceae. Epiphytic mosses are also ideal organisms for species modelling, because of having no roots, they are highly dependent on external environmental conditions. For this purpose, we used the ecological niche modelling approach to define their potential distribution in China and adjacent areas and explore factors that shape this distribution. We used 617 occurrence records of 23 species from six genera within the Orthotrichaceae family. Our results suggest that the distribution of members of the Orthotrichaceae family is predominantly affected by bioclimatic variables, especially bio10 (mean temperature of the warmest quarter), bio15 (precipitation seasonality), bio18 (precipitation of the warmest quarter), bio19 (precipitation of the coldest quarter), bio9 (mean temperature of the driest quarter), and bio2 (mean diurnal range). However, the distribution of particular genera is ruled by a different set of those variables. The distribution of two genera (Leratia and Ulota) is also highly influenced by land cover (especially mixed/other trees), whereas human footprint shows a moderate contribution to models of three genera (Lewinskya, Orthotrichum, Nyholmiella). Based on the occupied climatic niche and distribution patterns, representatives of the studied family are divided into two groups. The ‘western-montane group‘ is characterised by lower temperatures and lower precipitation whereas the ‘eastern-lowland’ group‘ by more humid and warmer conditions.
“…Epiphytic bryophytes are generally willing to occupy the bark of trees both in temperate forests and in more humid tropical areas [ 13 ]. With approximately 850 widely distributed subcosmopolitan species, the family Orthotrichaceae [ 14 , 15 , 16 , 17 , 18 , 19 , 20 , 21 , 22 ] is one of the main components of the cryptogam epiphytic communities and occurs on tree trunks and branches, and occasionally they are found also in saxicolous habitats. In Central and East Asia, the family is represented by eight genera, namely Leratia , Lewinskya , Macrocoma , Macromitrium , Nyholmiella , Orthotrichum , Ulota, and Zygodon , which can be found in most biomes, from tundra to wet tropical forests.…”
Epiphytes, including vascular and non-vascular, constitute a large part of global plant biodiversity. Distribution of obligatory epiphytic bryophytes results from climate and local habitat conditions. The most important epiphytic bryophytes and at the same time poorly investigated and taxonomically problematic ones belong to the family Orthotrichaceae. Epiphytic mosses are also ideal organisms for species modelling, because of having no roots, they are highly dependent on external environmental conditions. For this purpose, we used the ecological niche modelling approach to define their potential distribution in China and adjacent areas and explore factors that shape this distribution. We used 617 occurrence records of 23 species from six genera within the Orthotrichaceae family. Our results suggest that the distribution of members of the Orthotrichaceae family is predominantly affected by bioclimatic variables, especially bio10 (mean temperature of the warmest quarter), bio15 (precipitation seasonality), bio18 (precipitation of the warmest quarter), bio19 (precipitation of the coldest quarter), bio9 (mean temperature of the driest quarter), and bio2 (mean diurnal range). However, the distribution of particular genera is ruled by a different set of those variables. The distribution of two genera (Leratia and Ulota) is also highly influenced by land cover (especially mixed/other trees), whereas human footprint shows a moderate contribution to models of three genera (Lewinskya, Orthotrichum, Nyholmiella). Based on the occupied climatic niche and distribution patterns, representatives of the studied family are divided into two groups. The ‘western-montane group‘ is characterised by lower temperatures and lower precipitation whereas the ‘eastern-lowland’ group‘ by more humid and warmer conditions.
A total of 46 species and two varieties of the traditionally interpreted genus Orthotrichum are currently known to occur in China. They represent five genera, including Orthotrichum (29 species), Lewinskya (14 species and two varieties), and Nyholmiella and Leratia that are represented by a single species each. The fifth genus Florschuetziella, also consisting of only one species, F. scaberrima, is an entirely neglected representative of the China’s moss flora. A list of all accepted taxa is presented and for each taxon all literature records and herbarium specimens are enumerated for provinces in which they have been recorded, and their distribution is mapped. A key to determination of Chinese orthotrichalean mosses is presented. A chronological list of 63 species and varieties and two designations, O. catagonioides and O. microsporum which have never been validly published, reported from China in the years 1892–2020 is presented. Four species, Orthotrichum brasii, O. hooglandii, O. elegans and O. gymnostomum are excluded from the bryoflora of China and Lewinskya affinis var. bohemica and Orthotrichum schimperi are recorded for the first time from this country. Phytogeography of the Chinese taxa of the orthotrichalean mosses is considered and they are grouped into eight phytogeographical elements and five sub-elements.
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