Abstract: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 … Show more
“…The research was conducted in the summers of 2019 and 2020. Bryophytes from the family Orthotrichaceae were chosen as a model group of organisms, with regard to their frequency in the studied area and because they grow mostly epiphytically [ 42 , 67 ]. All deciduous trees were searched for bryophytes.…”
Section: Methodsmentioning
confidence: 99%
“…In addition, we compare the results with a neutral cover of the bark itself without bryophytes. We chose the family Orthotrichaceae as a model group of organisms with regard to their frequency in the studied area and their mostly epiphytical growth [ 42 ].…”
The pH of tree bark is affected by many factors, amongst them epiphytic bryophytes changing in their active state environment. Thus, we hypothesized that bryophytes can change bark acidity, dependently of the inclination of the branches, as inclination affect the water regime and particle deposition. We measured the pH under bryophyte cushions and compared it to nearby naked bark. Additionally, we compared results with experimental bark covering with neutral cover. We found that the pH of naked bark declines with decreasing inclination of trunks. Although bryophyte cover did not generally change the pH of the bark, there was a significant interaction with inclination: with higher inclination, bryophytes decrease the pH reaction of bark, while with lower inclination they increase it. One possible explanation may lie in changes to alkaline particle deposition, or conversely in the acidification of the bark by leaching. In addition, an experiment with a neutral cover showed that naked bark covering would substantially increase pH. As, on average, bryophytes do not change the pH of bark, there can be mutual interference between the alkalizing effect of the bark cover itself and the acidifying biological effect of bryophytes.
“…The research was conducted in the summers of 2019 and 2020. Bryophytes from the family Orthotrichaceae were chosen as a model group of organisms, with regard to their frequency in the studied area and because they grow mostly epiphytically [ 42 , 67 ]. All deciduous trees were searched for bryophytes.…”
Section: Methodsmentioning
confidence: 99%
“…In addition, we compare the results with a neutral cover of the bark itself without bryophytes. We chose the family Orthotrichaceae as a model group of organisms with regard to their frequency in the studied area and their mostly epiphytical growth [ 42 ].…”
The pH of tree bark is affected by many factors, amongst them epiphytic bryophytes changing in their active state environment. Thus, we hypothesized that bryophytes can change bark acidity, dependently of the inclination of the branches, as inclination affect the water regime and particle deposition. We measured the pH under bryophyte cushions and compared it to nearby naked bark. Additionally, we compared results with experimental bark covering with neutral cover. We found that the pH of naked bark declines with decreasing inclination of trunks. Although bryophyte cover did not generally change the pH of the bark, there was a significant interaction with inclination: with higher inclination, bryophytes decrease the pH reaction of bark, while with lower inclination they increase it. One possible explanation may lie in changes to alkaline particle deposition, or conversely in the acidification of the bark by leaching. In addition, an experiment with a neutral cover showed that naked bark covering would substantially increase pH. As, on average, bryophytes do not change the pH of bark, there can be mutual interference between the alkalizing effect of the bark cover itself and the acidifying biological effect of bryophytes.
“…Due to the fact that detailed research of epiphytic bryophytes was performed only on the area of tea plantations, we do not have relevant data available for comparison with the species diversity of bryophytes growing in other communities in the area. However, the observations in other regions show that the diversity of mosses growing epiphytically on old solitary trees, terrestrially on open soil or on the surface of stones along plantations is significantly lower 6,19,108 . This is mainly due to influence of the microclimatic conditions.…”
Section: Discussionmentioning
confidence: 94%
“…In addition, while O . stramineum was for long time considered to be a European species, it has been identified in North America 45 , 106 and later in China 108 .…”
Section: Discussionmentioning
confidence: 99%
“…Similarly, while O. stramineum has been reported only from the northern part of the country so far 100 , it was repeatedly observed in the southwestern part of the country in the present study. In addition, while O. stramineum was for long time considered to be a European species, it has been identified in North America 45,106 and later in China 108 . The vertical distribution of cryptogams of tea shrubs has not been the subject of research so far.…”
Bryophytes and lichens are outstanding bioindicators, not only of the plant community in which they develop, but also the substrates on which they grow. Some epiphytic cryptogams, particularly the rare ones, are stenotopic and require a long habitat continuity, for example substrates such as old trees. It could also be a tea plantation, this is because the shrubs are not felled, and most of them may have several dozen years. In addition, the shrubs are not subject to sudden changes in microclimatic conditions as only the young leaves are harvested. As the importance of tea plantations as host plants for mosses and lichens has not yet been studied, the present study examines the species diversity of cryptogams of two tea plantations in Georgia (Caucasus). The study also examines the phytogeography, spatial pattern, environmental conditions and ecological indicators of the cryptogams. Thirty-nine cryptogam taxa were identified; typical forest taxa dominated, even in the absence of typical forest communities. Some of these species are obligatory epiphytes, rare or even critically endangered in most European countries (e.g., Orthotrichum stellatum, O. stramineum, Lewinskya striata). The fairly abundant record of such species on tea plantations indicates the importance of these phytocoenoses for the preservation of rare species, and indicates that these habitats are hot spots for these cryptogams in otherwise changed envirnonment. Additionally, as indicated the analysis of the species composition of individual plantations and the mathematical analysis made on this basis, plantations differ from each other. Another interesting result is also the spatial distributions of cryptogams on tea bushes resemble those of forest communities and lichens seems to be more sensitive than bryophytes to antropogenic changes of environment.
Florschuetziella scaberrima (Broth.) Vitt, previously known only from the type material collected in 1915 from Yunnan, China, was rediscovered nearly a century later in 2005. The species is morphologically indistinguishable from the Mexican endemic F. steerei Vitt, but given the paucity of material the two are provisionally retained as distinct, allopatric species. Both species exhibit traits reminiscent of Leratia neocaledonica Broth. & Paris, a species endemic to New Caledonia. A shared ancestry with the other species currently accommodated in Leratia Broth. & Paris, i.e., L. exigua (Sull.) Goffinet and L. obtusifolia (Hook.) Goffinet, and the phylogenetically nested position of Florschuetziella Vitt within Leratia supports the merger of the two generic names, and hence the transfer of species of Florschuetziella, prompting the proposed new combinations Leratia steerei (Vitt) Goffinet, S.He & Shevock and Leratia scaberrima (Broth.) Goffinet, S.He & Shevock.
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