in

Tea plantations and their importance as host plants and hot spots for epiphytic cryptogams

[adace-ad id="91168"]
  • 1.

    Namita, P., Mukesh, R. & Vijay, K. J. Camellia Sinensis (Green Tea): A review. Glob. J. Pharmacol. 6(2), 52–59 (2012).

    Google Scholar 

  • 2.

    Chang, K. World Tea Production and Trade. Current and Future Development (FAO, Rome, 2015).

    Google Scholar 

  • 3.

    Chang, K. & Brattlof, M. World Tea Production and Trade. Current and Future Development (FAO, 2015).

    Google Scholar 

  • 4.

    Kochlamazashvili, I. & Kakulia, N. The Georgian Tea Sector: A Value Chain Study. ISET Policy Institute. Study prepared in the framework of ENPARD project Cooperation for Rural Prosperity in Georgia (2015).

  • 5.

    Lesica, P., McCune, B., Cooper, S. V. & Hong, W. S. Differences in lichen and bryophyte communities between old-growth and managed second-growth forests in the Svan Valley Montana. Can. J. Bot. 69, 1745–1755 (1991).

    Article 

    Google Scholar 

  • 6.

    Nowak, A., Plášek, V., Nobis, M. & Nowak, S. Epiphytic communities of open habitats in the Western Tian-Shan Mts (Middle Asia: Kyrgyzstan). Cryptog. Bryol. 37(4), 415–433 (2016).

    Article 

    Google Scholar 

  • 7.

    Rhoades, F. M. Nonvascular epiphytes in forest canopies: Worldwide distribution, abundance and ecological roles. In Forest Canopies (eds. Lowman, M.D. & Nadkarni, N. M.) 353–408 (1995).

  • 8.

    Haines, W. P. & Renwick, J. A. A. Bryophytes as food: Comparative consumption and utilization of mosses by a generalist insect herbivore. Entomol Exp Appl. 133, 296–306. https://doi.org/10.1111/j.1570-7458.2009.00929.x (2009).

    Article 

    Google Scholar 

  • 9.

    Kuřavová, K. et al. Is feeding on mosses by groundhoppers in the genus Tetrix (Insecta: Orthoptera) opportunistic or selective?. Arthropod-Plant Int. 11, 35–43. https://doi.org/10.1007/s11829-016-9461-9 (2017).

    Article 

    Google Scholar 

  • 10.

    Matuszkiewicz, W. Przewodnik do Oznaczania Zbiorowisk Roślinnych Polski (Wyd Nauk, PWN, 2001).

    Google Scholar 

  • 11.

    Krestov, P. V. Forest vegetation of easternmost Russia (Russian Far East). In Forest Vegetation of Northeast Asia (eds Kolbek, J. et al.) 93–180 (Springer, 2003).

    Chapter 

    Google Scholar 

  • 12.

    Kuznetsov, O. Topology-ecological classification of mire vegetation in the Republic of Karelia (Russia). In Biodiversity and Conservation of Boreal Nature. Proceedings of the 10 years anniversary symposium of the Nature Reserve Friendship (eds Heikkilä, R. & Lindholm, T.) 117–123 (Elsevier, 2003).

    Google Scholar 

  • 13.

    Černý, T. Phytosociological Study of Selected Critical Thermophilous Vegetation Complexes in the Czech Republic. A thesis submitted for the degree of Doctor of Philosophy in the Department of Botany Faculty of Sciences, Charles University (2007).

  • 14.

    Chytrý, M. et al. A modern analogue of the Pleistocene steppe-tundra ecosystem in southern Siberia. Boreas 48, 36–56 (2019).

    Article 

    Google Scholar 

  • 15.

    Wolski, G. J. & Kruk, A. Determination of plant communities based on bryophytes: The combined use of Kohonen artificial neural network and indicator species analysis. Ecol. Indic 113, 106160. https://doi.org/10.1016/j.ecolind.2020.106160 (2020).

    Article 

    Google Scholar 

  • 16.

    Benzing, D. Vulnerabilities of tropical forests to climate change: The significance of resident epiphytes. Clim. Change 39, 519–540 (1998).

    Article 

    Google Scholar 

  • 17.

    Gustafsson, L., Fiskesjö, A., Ingelög, T., Petterson, B. & Thor, G. Factors of importance to some lichen species of deciduous broad-leaved woods in southern Sweden. Lichenologist 24, 255–266 (1992).

    Article 

    Google Scholar 

  • 18.

    Frahm, J. P. Ecology of bryophytes along altitudinal and latitudinal gradients in Chile. Trop. Bryol. 21, 67–79 (2002).

    Google Scholar 

  • 19.

    Číhal, L., Kaláb, O. & Plášek, V. Modeling the distribution of rare and interesting moss species of the family Orthotrichaceae (Bryophyta) in Tajikistan and Kyrgyzstan. Acta Soc. Bot. Pol. 86(2), 3543. https://doi.org/10.5586/asbp.3543 (2017).

    Article 

    Google Scholar 

  • 20.

    Łubek, A., Kukwa, M., Czortek, P. & Jaroszewicz, B. Impact of Fraxinus excelsior dieback on biota of ash-associated lichen epiphytes at the landscape and community level. Biodivers. Conserv. 29, 431–450. https://doi.org/10.1007/s10531-019-01890-w (2020).

    Article 

    Google Scholar 

  • 21.

    Łubek, A., Kukwa, M., Jaroszewicz, B. & Czortek, P. Identifying mechanisms shaping lichen functional diversity in a primeval forest. For. Ecol. Manag. 475, 118434. https://doi.org/10.1016/j.foreco.2020.118434 (2020).

    Article 

    Google Scholar 

  • 22.

    Barkman, J. J. Phytosociology and Ecology of Cryptogamic Epiphytes. Including a Taxonomic Survey and Description of Their Vegetation Units in Europe, Van Gorcum, Comp (N. V Assen, 1958).

    Google Scholar 

  • 23.

    Green, T. G. A. & Lange, O. L. Photosynthesis in poikilohydric plants: A comparison of lichens and bryophytes. In Ecophysiology of Photosynthesis (eds Schulze, E.-D. & Caldwell, M. M.) 319–341 (Springer-Verlag, 1995).

    Chapter 

    Google Scholar 

  • 24.

    Scheidegger, C., Wolseley, P. A. & Landolt, R. Towards conservation of lichens. Forest. Snow Landsc. Res. 75, 285–433 (2000).

    Google Scholar 

  • 25.

    Tønsberg, T. & Høiland, K. A study of the macrolichen flora on the sand-dune areas on Lista, SW Norway. Nor. J. Bot. 27, 131–134 (1980).

    Google Scholar 

  • 26.

    Thiet, R. K., Doshas, A. & Smith, S. M. Effects of biocrusts and lichen-moss mats on plant productivity in a US sand dune ecosystem. Plant Soil 377(1), 235–244 (2014).

    CAS 
    Article 

    Google Scholar 

  • 27.

    Vaz, A. S., Marques, J. & Honrado, J. P. Patterns of lichen diversity in coastal sand-dunes of northern Portugal. Bot. Complut. 38, 89–96 (2014).

    Article 

    Google Scholar 

  • 28.

    Antoninka, A., Bowker, M. A., Reed, S. C. & Doherty, K. Production of greenhouse-grown biocrust mosses and associated cyanobacteria to rehabilitate dryland soil function. Restor. Ecol. 24(3), 324–335 (2016).

    Article 

    Google Scholar 

  • 29.

    Jüriado, I., Kämärä, M.-L. & Oja, E. Environmental factors and ground disturbance affecting the composition of species and functional traits of ground layer lichens on grey dunes and dune heaths of Estonia. Nord. J. Bot. 34(2), 244–255 (2016).

    Article 

    Google Scholar 

  • 30.

    Balogh, R. et al. Mosses and lichens in dynamics of acidic sandy grasslands: Specific response to grazing exclosure. Acta Biol. Plant. Agriensis 5(1), 30 (2017).

    Google Scholar 

  • 31.

    Concostrina-Zubiri, L., Arenas, J. M., Martínez, I. & Escudero, A. Unassisted establishment of biological soil crusts on dryland road slopes. Web Ecol. 19(1), 39–51 (2019).

    Article 

    Google Scholar 

  • 32.

    Kubiak, D. & Oszyczka, P. Non-forested vs forest environments: The effect of habitat conditionson host tree parameters and the occurrence of associated epiphytic lichens. Fungal Ecol. 47, 100957 (2020).

    Article 

    Google Scholar 

  • 33.

    Gradstein, S. R. & Sporn, S. G. Land-use change and epiphytic bryophyte diversity in the Tropics. Nova Hedwigia 138, 311–323 (2010).

    Google Scholar 

  • 34.

    Guevara, S., Purata, S. E. & Van der Maarel, E. The role of remnant forest trees in tropical secondary succession. Vegetatio 66, 77–84 (1986).

    Google Scholar 

  • 35.

    Sillett, S. C., Gradstein, S. R. & Griffin, D. Bryophyte diversity of Ficus tree crowns from cloud forest and pasture in Costa Rica. Bryologist 98(2), 251–260 (1995).

    Article 

    Google Scholar 

  • 36.

    Werner, F., Homeier, J. & Gradstein, S. R. Diversity of vascular epiphytes on isolated remnant trees in the montane forest belt of southern Ecuador. Ecotropica 11, 21–40 (2005).

    Google Scholar 

  • 37.

    Lara, F., Garilleti, R. & Mazimpaka, V. Orthotrichum karoo (Orthotrichaceae), a new species with hyaline-awned leaves from southwestern Africa. Bryologist 112(1), 194–201 (2009).

    Article 

    Google Scholar 

  • 38.

    Lara, F. & Mazimpaka, V. Ma´s sobre la presencia de Orthotrichum acuminatum en la Península Ibérica. Cryptog. Bryol. Lichenol. 13(4), 349–354 (1992).

    Google Scholar 

  • 39.

    Garilleti, R., Lara, F. & Mazimpaka, V. Orthotrichum anodon (Orthotrichaceae, Bryopsida), a new species from California, and its relationships with other Orthotricha sharing puckered capsule mouths. Bryologist 109(2), 188–196 (2006).

    Article 

    Google Scholar 

  • 40.

    Hallingbäck, T. & Hodgetts, N. Mosses Liverworts and Hornworts. Status survey and conservation action plan for bryophytes (Cambridge University Press, 2000).

    Google Scholar 

  • 41.

    Belinchón, R., Martínez, I., Escudero, A., Aragón, G. & Valladares, F. Edge effects on epiphytic communities in a Mediterranean Quercus pyrenaica forest. J. Veg. Sci. 18, 81–90. https://doi.org/10.1111/j.1654-1103.2007.tb02518.x (2007).

    Article 

    Google Scholar 

  • 42.

    Boudreault, C., Gauthier, S. & Bergeron, Y. Epiphytic lichens and bryophytes on Populus Tremuloides along a chronosequence in the Southwestern Boreal Forest of Quebec, Canada. Bryologist 103, 725–738. https://doi.org/10.1639/0007-2745(2000)103[0725:ELABOP]2.0.CO;2 (2009).

    Article 

    Google Scholar 

  • 43.

    Rambo, T. Structure and composition of corticolous epiphyte communities in a Sierra Nevada old-growth mixed-conifer forest. Bryologist 113, 55–71. https://doi.org/10.1639/0007-2745-113.1.55 (2010).

    Article 

    Google Scholar 

  • 44.

    Plášek, V., Nowak, A., Nobis, M., Kusza, G. & Kochanowska, K. Effect of 30 years of road traffic abandonment on epiphytic moss diversity. Environ. Monit. Assess. 186, 8943–8959. https://doi.org/10.1007/s10661-014-4056-3 (2014).

    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 45.

    Skoupá, Z., Ochyra, R., Guo, S. L., Sulayman, M. & Plášek, V. Distributional novelties for Lewinskya, Nyholmiella and Orthotrichum (Orthotrichaceae) in China. Herzogia 30, 58–73. https://doi.org/10.13158/heia.30.1.2017.58 (2017).

    Article 

    Google Scholar 

  • 46.

    Skoupá, Z., Ochyra, R., Guo, S.-L., Sulayman, M. & Plášek, V. Three remarkable additions of Orthotrichum species (Orthotrichaceae) to the moss flora of China. Herzogia 31, 88–100. https://doi.org/10.13158/099.031.0105 (2018).

    Article 

    Google Scholar 

  • 47.

    Gradstein, R. et al. Bryophytes of Mount Patuha, West Java, Indonesia. Reinwardtia 13(2), 107–123 (2010).

    Google Scholar 

  • 48.

    Saat, A., Talib, M. S., Harun, N., Hamzah, Z. & Wood, A. K. Spatial variability of arsenic and heavy metals in a highland tea plantation using lichens and mosses as bio-monitors. Asian J. Nat. Appl. Sci. 5(1), 10–21 (2016).

    Google Scholar 

  • 49.

    Fick, S. E. & Hijmans, R. J. WorldClim 2: New 1km spatial resolution climate surfaces for global land areas. Int. J. Climatol. 37(12), 4302–4315 (2017).

    Article 

    Google Scholar 

  • 50.

    Wirth, V. Ökologische Zeigerwerte von Flechten. Herzogia 23(2), 229–248 (2010).

    Article 

    Google Scholar 

  • 51.

    Ellenberger, H. et al. Zeigerwerte von Planzen in Mitteleuropa. Scr. Geobot. 18, 1–248 (1991).

    Google Scholar 

  • 52.

    Smith, C. W. et al. The Lichens of Great Britain and Ireland 1046 (British Lichen Society, 2009).

    Google Scholar 

  • 53.

    Hodgetts, N. et al. An annotated checklist of bryophytes of Europe, Macaronesia and Cyprus. J. Bryol. 42(1), 1–116. https://doi.org/10.1080/03736687.2019.1694329 (2020).

    Article 

    Google Scholar 

  • 54.

    Pancho, J. V. Some bryophytes in tea plantations, Pagilaran Central Java. Biotrop. Bull. 11, 279–282 (1979).

    Google Scholar 

  • 55.

    Tan, B. C. et al. Mosses of Gunung Halimun National Park, West Java, Indonesia. Reinwardtia 12, 205–214 (2006).

    Google Scholar 

  • 56.

    Ohsawa, M. Weeds of tea plantations. In Biology and Ecology of Weeds. Geobotany Vol. 2 (eds Holzner, W. & Numata, M.) (Springer, 1982).

    Google Scholar 

  • 57.

    Gradstein, R. et al. Bryophytes of Mount Patuha, West Java, Indonesia. Reinwardtia 13, 107–123 (2010).

    Google Scholar 

  • 58.

    Whitelaw, M. & Burton, M. A. S. Diversity and distribution of epiphytic bryophytes on Bramley’s Seedling trees in East of England apple orchards. Glob. Ecol. Conserv. 4, 380–387. https://doi.org/10.1016/j.gecco.2015.07.014 (2015).

    Article 

    Google Scholar 

  • 59.

    Söderström, L. Bryophytes and decaying wood – a comparison between manager and natural forest. Holarc. Ecol. 14, 121–130 (1991).

    Google Scholar 

  • 60.

    Cieśliński, S. et al. Relikty lasu puszczańskiego, In Białowieski Park Narodowy (1921–1996) w badaniach geobotanicznych. Phytocoenosis, 8 (N.S.), Seminarium Geobotanicum (ed. Faliński, J. B.) 4, 47–64 (1996).

  • 61.

    Vanderpoorten, A., Engels, P. & Sotiaux, A. Trends in diversity and abundance of obligate epiphytic bryophytes in a highly managed landscape. Ecography 27, 567–576 (2004).

    Article 

    Google Scholar 

  • 62.

    Ódor, P., van Dort, K., Aude, E., Heilmann-Clausen, J. & Christensen, M. Diversity and composition of dead wood inhabiting bryophyte communities in European beech forest. Biol. Soc. Esp. Briol. 26–27, 85–102 (2005).

    Google Scholar 

  • 63.

    Friedel, A., Oheimb, G. V., Dengler, J. & Härdtle, W. Species diversity and species composition of epiphytic bryophytes and lichens: A comparison of managed and unmanaged beech forests in NE Germany. Feddes Repert. 117(1–2), 172–185 (2006).

    Article 

    Google Scholar 

  • 64.

    Wolski, G. J. Siedliskowe Uwarunkowania Występowania Mszaków w Rezerwatach Przyrody Chroniących Jodłę Pospolitą w Polsce Środkowej (Praca doktorska wykonana w Katedrze Geobotaniki i Ekologii Roślin UŁ, 2013).

    Google Scholar 

  • 65.

    Fudali, E. & Wolski, G. J. Ecological diversity of bryophytes on tree trunks in protected forests (a case study from Central Poland). Herzogia 28(1), 91–107 (2015).

    Article 

    Google Scholar 

  • 66.

    Shi, X.-M. et al. Epiphytic bryophytes as bio-indicators of atmospheric nitrogen deposition in a subtropical montane cloud forest: Response patterns, mechanism, and critical load. Environ. Pollut. 229, 932–941. https://doi.org/10.1016/j.envpol.2017.07.077 (2017).

    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 67.

    Cornelissen, J. H. C. & Gradstein, S. R. On the occurrence of bryophytes and macrolichens in different lowland rain forest types of Mabura Hill, Guyana. Trop. Bryol. 3, 29–35. https://doi.org/10.11646/bde.3.1.4 (1990).

    Article 

    Google Scholar 

  • 68.

    Lyons, B., Nadkarni, N. M. & North, M. P. Spatial distribution and succession of epiphytes on Tsuga heterophylla (western hemlock) in an old-growth Douglas-fir forest. Can. J. Bot. 78(7), 957–968. https://doi.org/10.1139/cjb-78-7-957 (2000).

    Article 

    Google Scholar 

  • 69.

    Cornelissen, J. H. C. & Steege, H. T. Distribution and ecology of epiphytic bryophytes and lichens in dry evergreen forest of Guyana. J. Trop. Ecol. 5, 131–150. https://doi.org/10.1017/S0266467400003400 (1989).

    Article 

    Google Scholar 

  • 70.

    Woods, C. L., Cardelús, C. L., Dewalt, S. J. & Piper, F. Microhabitat associations of vascular epiphytes in a wet tropical forest canopy. J. Ecol. 103(2), 421–430. https://doi.org/10.1111/1365-2745.12357 (2015).

    Article 

    Google Scholar 

  • 71.

    Sporn, S. G., Bos, M. M., Kessler, M. & Gradstein, S. R. Vertical distribution of epiphytic bryophytes in an Indonesian rainforest. Biodivers. Conserv. 19(3), 745–760. https://doi.org/10.1007/s10531-009-9731-2 (2010).

    Article 

    Google Scholar 

  • 72.

    Czerepko, J. et al. How sensitive are epiphytic and epixylic cryptogams as indicators of forest naturalness? Testing bryophyte and lichen predictive power in stands under different management regimes in the Białowieża forest. Ecol. Indic. 125, 107532. https://doi.org/10.1016/j.ecolind.2021.107532 (2021).

    Article 

    Google Scholar 

  • 73.

    Putna, S. & Mězaka, A. Preferences of epiphytic bryophytes for forest stand and substrate in North-East Latvia. Folia Cryptog. Estonica 51, 75–83 (2014).

    Article 

    Google Scholar 

  • 74.

    Manakyan, V. A. Results of bryological studies in Armenia. Arctoa 5, 15–33 (1995).

    Article 

    Google Scholar 

  • 75.

    Redfearn, P. L., Tan, B. C. & He, S. A newly updated and annotated checklist of Chines mosses. J. Hattori Bot. Lab. 79, 163–357 (1996).

    Google Scholar 

  • 76.

    Kürschner, H. Bryophyte Flora of the Arabian Peninsula and Socotra. Bryophytorum Bibliotheca (JCramer in der Gebrüder Borntraeger Verlagsbuchhandlung, 2000).

    Google Scholar 

  • 77.

    Higuchi, M. & Nishimura, N. Mosses of Pakistan. J. Hattori Bot. Lab. 93, 273–291 (2003).

    Google Scholar 

  • 78.

    Ignatov, M. S., Afonina, O. M. & Ignatova, E. A. Check-list of mosses of East Europe and North Asia. Arctoa 15, 1–130. https://doi.org/10.15298/arctoa.15.01 (2006).

    Article 

    Google Scholar 

  • 79.

    Sabovljević, M. et al. Check-list of the mosses of SE Europe. Phytol. Balcan. 14(2), 207–244 (2008).

    Google Scholar 

  • 80.

    Dandotiya, D., Govindapyari, H., Suman, S. & Uniyal, P. L. Checklist of the bryophytes of India. Arch. Bryol. 88, 71–72 (2011).

    Google Scholar 

  • 81.

    Hodgetts, N. G. Checklist and Country Status of European bryophytes—Towards a New Red List for Europe. Irish Wildlife Manuals, No. 84. (National Parks and Wildlife Service, Department of Arts, Heritage and the Gaeltacht, 2011). https://www.hdl.handle.net/2262/73373.

  • 82.

    Kürschner, H. & Frey, W. Liverworts, Mosses and Hornworts of Southwest Asia (Marchantiophyta, Bryophyta, Anthoceroptophyta). Nova Hedwigia 139, 179–180 (2011).

    Google Scholar 

  • 83.

    Suzuki, T. A revised new catalog of the mosses of Japan. Hattoria 7, 9–223. https://doi.org/10.18968/hattoria.7.0_9 (2016).

    Article 

    Google Scholar 

  • 84.

    Kürschner, H. & Frey, W. Liverworts, mosses and hornworts of Afghanistan—our present knowledge. Acta Mus. Siles. Sci. Natur. 68, 11–24 (2019).

    Google Scholar 

  • 85.

    Brotherus, V. F. Enumeratio muscorum Caucasi. Acta Soc. Sci. Fenn. 19, 1–170 (1892).

    Google Scholar 

  • 86.

    Chikovani, N. & Svanidze, T. Checklist of bryophyte species of Georgia. Braun-Blanquetia 34, 97–116. https://doi.org/10.13158/heia.26.1.2013.213 (2004).

    Article 

    Google Scholar 

  • 87.

    Doroshina, G. Y. New moss records from Georgia. 1. Arctoa 19, 281 (2010).

    Google Scholar 

  • 88.

    Sohrabi, M., Ahti, T. & Urbanavichus, G. Parmelioid lichens of Iran and the caucasus Region. Mycol. Balc. 4, 21–30 (2007).

    Google Scholar 

  • 89.

    Hawksworth, D. L., Blanco, O., Divakar, P. K., Ahti, T. & Crespo, A. A first checklist of parmelioid and similar lichens in Europe and some adjacent territories, adopting revised generic circumscriptions and with indications of species distributions. Lichenologist 40(1), 1–21. https://doi.org/10.1017/S0024282908007329 (2008).

    Article 

    Google Scholar 

  • 90.

    Syrek, M. & Kukwa, M. Taxonomy of the lichen Cladonia rei and its status in Poland. Biologia 63(4), 493–497. https://doi.org/10.2478/s11756-008-0092-1 (2008).

    Article 

    Google Scholar 

  • 91.

    Burgaz, A. R., Ahti, T., Inashvili, T., Batsatsashvili, K. & Kupradze, I. Study of georgian Cladoniaceae. Bot. Complut. 42, 19–55. https://doi.org/10.5209/BOCM.61367 (2018).

    Article 

    Google Scholar 

  • 92.

    Fałtynowicz, W. The lichens, lichenicolous and allied fungi of Poland. An annotated checklist. In Biodiversity of Poland (ed. Mirek, A.) 1–435 (W. Szafer Institute of Botany, Polish Academy of Sciences, 2003).

    Google Scholar 

  • 93.

    Plášek, V., Sawicki, J., Ochyra, R., Szczecińska, M. & Kulik, T. New taxonomical arrangement of the traditionally conceived genera Orthotrichum and Ulota (Orthotrichaceae, Bryophyta). Acta Mus. Sil. 64, 169–174. https://doi.org/10.1515/cszma-2015-0024 (2015).

    Article 

    Google Scholar 

  • 94.

    Lara, F. et al. Lewinskya, a new genus to accommodate the phaneroporous and monoicous taxa of Orthotrichum (Bryophyta, Orthotrichaceae). Cryptog. Bryol. 37, 361–382. https://doi.org/10.7872/cryb/v37.iss4.2016.361 (2016).

    Article 

    Google Scholar 

  • 95.

    Sawicki, J. et al. Mitogenomic analyses support the recent division of the genus Orthotrichum (Orthotrichaceae, Bryophyta). Sci. Rep. 7, 4408. https://doi.org/10.1038/s41598-017-04833-z (2017).

    ADS 
    CAS 
    Article 
    PubMed 
    PubMed Central 

    Google Scholar 

  • 96.

    Kürschner, H., Batsatsashvili, K. & Parolly, G. Noteworthy additions to the bryophyte flora of Georgia. Herzogia 26, 213–216. https://doi.org/10.13158/heia.26.1.2013.213 (2013).

    Article 

    Google Scholar 

  • 97.

    Ellis, L. T. et al. New national and regional bryophyte records, 49. J. Bryol. 38(4), 327–347 (2016).

    Article 

    Google Scholar 

  • 98.

    Ellis, L. T. et al. New national and regional bryophyte records, 51. J. Bryol. 39(2), 177–190 (2017).

    Article 

    Google Scholar 

  • 99.

    Eckstein, J., Garilleti, R. & Lara, F. Lewinskya transcaucasica (Orthotrichaceae, Bryopsida) sp. nov. A contribution to the bryophyte flora of Georgia. J. Bryol. 40(1), 31–38. https://doi.org/10.1080/03736687.2017.1365218 (2018).

    Article 

    Google Scholar 

  • 100.

    Eckstein, J. & Zündorf, H.-J. Orthotrichaceous mosses (Orthotricheae, Orthotrichaceae) of the Genera Lewinskya, Nyholmiella, Orthotrichum, Pulvigera and Ulota Contributions to the bryophyte flora of Georgia 1. Cryptog. Bryol. 38(4), 365–382. https://doi.org/10.7872/cryb/v38.iss4.2017.365 (2017).

    Article 

    Google Scholar 

  • 101.

    Schäfer-Verwimp, A. Orthotrichum Hedw. In Die Moose Baden-Württembergs. Band 2: Spezieller Teil (Bryophytina II, Schistostegales bis Hypnobryales) (eds Nebel, M. & Philippi, G.) 170–197 (Eugen Ulmer, 2001).

    Google Scholar 

  • 102.

    Lara, F. & Garilleti, R. Orthotrichum Hedw. In Flora briofítica Ibérica (eds Guerra, J. & Brugués, C. M.) 50–135 (Universidad de Murcia Sociedad Española de Briología, 2014).

    Google Scholar 

  • 103.

    Lewinsky, J. The genus Orthotrichum Hedw. (Orthotrichaceae, Musci) in Southeast Asia. A taxonomic revision. J. Hattori Bot. Lab. 72, 1–88 (1992).

    Google Scholar 

  • 104.

    Schäfer-Verwimp, A. & Gruber, J. P. Orthotrichum (Orthotrichaceae, Bryopsida) in Pakistan. Trop. Bryol. 21, 1–9. https://doi.org/10.11646/bde.21.1.2 (2002).

    Article 

    Google Scholar 

  • 105.

    Draper, I., Mazimpaka, V., Albertos, B., Garilleti, R. & Lara, F. A survey of the epiphytic bryophyte flora of the Rif and Tazzeka Mountains (northern Morocco). J. Bryol. 27, 23–34. https://doi.org/10.1179/174328205X40554 (2005).

    Article 

    Google Scholar 

  • 106.

    Brassard, G. R. Orthotrichum stramineum new to North America. Bryologist 87, 168 (1984).

    Article 

    Google Scholar 

  • 107.

    Lewinsky-Haapasaari, J. & Long, D. G. Orthotrichum stramineum Hornsch. new to China. J. Bryol. 19, 350–352. https://doi.org/10.1179/jbr.1996.19.2.350 (1996).

    Article 

    Google Scholar 

  • 108.

    Plášek, V. et al. A synopsis of Orthotrichum s. lato (Bryophyta, Orthotrichaceae) in China, with distribution maps and a key to determination. Plants 10, 499. https://doi.org/10.3390/plants10030499 (2021).

    Article 
    PubMed 
    PubMed Central 

    Google Scholar 


  • Source: Ecology - nature.com

    Researchers design sensors to rapidly detect plant hormones

    Microdiversity characterizes prevalent phylogenetic clades in the glacier-fed stream microbiome