Grimmia ulaandamana (Grimmiaceae), a new moss species from China

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Ann. Bot. Fennici 50: 233 238 ISSN 0003-3847 (print) ISSN 1797-2442 (online) Helsinki 14 June 2013 Finnish Zoological and Botanical Publishing Board 2013 Grimmia ulaandamana (Grimmiaceae), a new moss species from China Chao Feng 1, Jesús Muñoz 2,3, Jin Kou 1 & Xue-Liang Bai 1, * 1) Department of Biology, College of Life Sciences, Inner Mongolia University, Hohhot, China (*corresponding author s e-mail: hujiaof@sina.com) 2) Real Jardín Botánico (RJB-CSIC), Plaza de Murillo 2, ES-28014 Madrid, Spain 3) Centro de Investigación de la Biodiversidad y Cambio Climático (BioCamb), Universidad Tecnológica Indoamérica, Calle Machala y Sabanilla, Quito, Ecuador Received 12 Dec. 2012, final version received 19 Mar. 2013, accepted 21 Mar. 2013 Feng, C., Muñoz, J., Kou, J. & Bai, X. L. 2013: Grimmia ulaandamana (Grimmiaceae), a new moss species from China. Ann. Bot. Fennici 50: 233 238. A new species of Grimmia (Grimmiaceae), G. ulaandamana J. Muñoz, C. Feng, X.L. Bai & J. Kou, from several localities in China, is described and illustrated. It is distinguished from all congeners in having 2 4(5)-stratose and V-shaped lamina, semi-terete to terete costa consisting of almost homogeneous cells and with four guide cells at mid-leaf, and a long plication in lower part on one or both sides of the leaf. Grimmia is one of the largest genera of the moss family Grimmiaceae. The number of species accepted in the genus, as traditionally considered, ranges from 51 (Maier 2010) to 71 (Muñoz & Pando 2000) or 95 (Hastings & Greven 2007). Ochyra et al. (2003) divided Grimmia into several smaller genera, some of them supported by the DNA sequence data (Hernández-Maqueda et al. 2008a, 2008b), but that taxonomy has not yet been widely accepted. Grimmia s. lato species grow on all continents, and most species are drought-resistant mosses that can withstand very dry and cold climates. The genus was considered taxonomically difficult, although recent studies have shown that the characters of the costa as seen in cross-section are crucial for correct identification, while variation in hair-point length, or shape of distal leaf cells, widely used in the past, are not reliable (Deguchi 1978, Maier & Geissler 1995, Muñoz 1998, Nyholm 1998, Muñoz & Pando 2000, Maier 2002a, 2002b, 2010, Ignatova & Muñoz 2005). During bryological work in China, we discovered several specimens of Grimmia different from any species previously reported from the area (Cao & Vitt 1986, Cao 2000, Cao et al. 2003). The specimens are characterized by 2 4(5)-stratose, strongly keeled leaves with a long plication in one or both sides of the lower half, a long, smooth and occasionally decurrent hair-point, and a semi-terete to terete costa consisting of almost homogeneous cells. Identical plants were found among collections kept in herbaria. These specimens do not match morphologically any described species. Grimmia ulaandamana J. Muñoz, C. Feng, X.L. Bai & J. Kou, sp. nova (Figs. 1 2) Type: People s Republic of China. Inner Mongolia, Ulaan dam Shipeng Ditch National Nature Reserve, Wanghuolou Mountain, 44 26 519 N, 118 45 955 E, on rocks, mixed with Macromitrium japonicum, 1967 m, 12 July 2011,

234 Feng et al. Ann. BOT. Fennici Vol. 50 Fig. 1. Grimmia ulaandamana (from the holotype). A: Plant when dry, the length for each frame is 1 mm. B: Cross-section of stem. C and D: Leaves (arrows: plicae in lower part of leaf). E: Hair-points. F: Apical part of leaf. G: Upper-leaf cells. H: Mid-leaf cells. I: Basal juxtacostal cells. J: Basal marginal cells. Scale bar (in B): 50 µm for B, E and F J; 1 mm for A, C and D. Chao Feng 2011527-2 (holotype HIMC; isotype MA-Musci 40053). Paratypes: China. Heilongjiang Province, Xin Ling Xian, 51 70 05 N, 124 40 05 E, C. Gao 13168 (ALTA); Inner Mongolia, Ulaan dam, the peak of Wanghuolou Mt., on rock, 12 July 2011 Xue-Liang Bai 2011485 (HIMC); Shaanxi Province, Hu Xian, Guang Tao Mts., 34 10 05 N, 108 60 05 E, M. Wang 462 (KUN); Hebei Province, Wuling Mt., 40 78 38 N, 117 50 05 E, J.-X. Ji C38 (ALTA); Yunnan Province, Lijiang Xian, Yu Loung Mts., 27 15 05 N, 100 20 05 E, X.-J. Li 80-147 (KUN).

Ann. BOT. Fennici Vol. 50 Grimmia ulaandamana, a new moss species from China 235 Fig. 2. Grimmia ulaandamana (from the holotype). A G: Cross-section of leaves, sequentially from apex to middle. H and I: Cross-section of lower part of leaves. Scale bar (in I): 50 µm for A E and G; 100 µm for F, H and I.

236 Feng et al. Ann. BOT. Fennici Vol. 50 Etymology. The specific epithet refers to one of the places where the new species was found, Ulaan dam. Plants medium-sized, stiff and rigid, forming small loose or dense cushions, olive-, dark- to blackish green. Stems 1.5 4.0 cm long, erect or weakly ascending when long, usually scarcely and irregularly branched, in transverse section rounded, consisting of (1)2 3(5)-stratose epidermis of small, thick-walled and orange-colored cells, distinct from large, thin-walled, hyaline medullar cells arranged in 4 6 layers, and a distinct central strand of 15 25 small, thin-walled cells. Leaves erect, appressed to slightly flexuose when dry, erect, patent to slightly spreading, rigid and not flexuose when moist, lanceolate or with an ovate base extended into an acuminate apical part, strongly keeled along costa, most often with a strong and long plication in one or both sides at proximal half, 1.60 3.45 0.30 0.75 mm; costa smooth, percurrent, semi-terete to nearly terete, protruding from lamina and regularly curved in outline on dorsal surface, clearly delimited from lamina, in distal half consisting of almost undifferentiated cells in 4 5 layers, usually only ventral band, composed of 2 slightly larger cells, scarcely differentiated from remaining cells, which are not differentiated in bands, in central and lower parts 4 6 layers, ventral layer differentiated from 1 2 dorsal layers and a band of 3 4 layers of substereids, at insertion 2 4 layers with ventral layer clearly differentiated from others; margins entire, recurved on one or occasionally both sides, flat distally, in medial and distal leaf 2 4-stratose; leaf lamina smooth or occasionally weakly pseudopapillose, 3 4(5)-stratose in distal part, 2-stratose in medial part; laminal cells moderately thick-walled, in distal part ovate, isodiametric or oblate, esinuose, 7.2 8.0 4.9 5.3 µm; in medial and basal parts rectangular, distinctly to strongly sinuose in broadest part of leaf, 9.1 12.5 6.5 7.8 µm; basal marginal cells chlorophyllose, isodiametric to shortly rectangular, 9.1 13.0 7.8 10.4 µm, walls straight or more or less sinuose, transverse walls thicker than longitudinal walls; basal juxtacostal cells elongate to rectangular, 31.2 57.2 6.5 13.0 µm, with thin to slightly thick, weakly nodulose walls; hair-points terete or slightly flattened at base and then decurrent, straight, not flexuose, to 1.7 mm long, entire to denticulate. Propagula lacking. Dioicous. Unfortunately, only one sporophyte attached to the plant was available, and it was old and in such a poor condition that it was not valid for description. Another complete capsule was found among the debris of one specimen, but without connection to the gametophytes and without seta. That capsule differs from that of any other Chinese Grimmia, and it could belong to G. ulaandamana. It is 1.5 0.6 mm, smooth, with a compound and revoluble annulus of 2 3 rows of isodiametric cells, and with a longrostrate operculum nearly 1 mm long. Habitat and distribution. Grimmia ulaandamana occurs on rocks in white-birch forests or on exposed rocks in open habitats. It is scattered over a large area in China (Fig. 3), including Xin Ling Xian in Heilongjiang, Wanghuolou Range in Inner Mongolia, Hu Xian and Guang Tao Mts. in Shaanxi, Wuling Mountain in Hebei and Lijiang Xian and Yu Loung Mts. in Yunnan. Grimmia ulaandamana is characterized by the regularly 2 4(5)-stratose upper leaf lamina, the strongly keeled leaves with recurved margins, the costa with a regularly curved dorsal outline and homogeneous cells except at the insertion, where it has two guide cells and lacks a ventral furrow, and the two plicae, one at each side of the costa, in the lower half of leaf. Among Grimmia, no species share this combination of characters (cf. Maier 2010). Grimmia montana and G. elatior share with G. ulaandamana the 2 4(5)-stratose lamina and the costa protruding dorsally from the lamina. Grimmia montana however differs from G. ulaandamana by its plane to incurved margins, and the costa with a clear band of hydroids in the lower half of leaf, that then become substereids for a short length, and disappear apically. Grimmia elatior also shares with G. ulaandamana the undifferentiated cells of the costa in cross-section; however, it is a much larger plant, reaching 8 cm long, it has longrectangular juxtacostal cells with strongly nodulose walls, papillose median and distal cells, the costa is irregularly shaped dorsally, flattened and angulate, and at the insertion the costa has four or more guide cells and still has a narrow ventral furrow, lacking in G. ulaandamana. Grimmia khasiana (considered synonymous with G. longirostris by Muñoz & Pando 2000,

Ann. BOT. Fennici Vol. 50 Grimmia ulaandamana, a new moss species from China 237 Fig. 3. Black dots: known localities of Grimmia ulaan damana. Yellow dots: localities from which Grimmia specimens have been studied by JM. but treated as a distinct species by Maier 2010), G. longirostris, G. ovalis and G. unicolor are similar to G. ulaandamana in having a 2 4-stratose leaf lamina, but in those species the costa is wider, having more than four guide cells at the insertion, it does not protrude dorsally from the lamina as in G. ulaandamana, and in crosssection there is always a band of hydroids in the basal half of the leaf. Grimmia ulaandamana is also characterized by having a distinctive plication on both sides in the leaf base (Figs. 1C, D and 2H, I), running up to mid-leaf. In Grimmia, only G. alpestris, G. caespiticia and G. reflexidens (treated as G. sessitana by Maier 2010) can have plicate leaves, but in those species, like in the plicate Coscinodon, the plications run from the medial part towards the apex (Hastings 1996, Hastings 2007), not to the base as in G. ulaandamana. Acknowledgements The study was supported by the Natural Science Foundation of China (grant nos. 30870160, 31011120089, 31170497) and the Ministry of Science and Technology of Spain (grant CGL2009-09530-BOS). References Cao, T. 2000. Grimmiaceae. In: Li, X. J. (ed.), Flora Bryophytorum Sinicorum: 1 80. Science Press. Beijing. Cao, T. & Vitt, D. H. 1986: A taxonomic revision and phylogenetic analysis of Grimmia and Schistidium (Bryopsida; Grimmiaceae) in China. Journal of the Hattori Botanical Laboratory 61: 123 247. Cao, T., He, S. & Vitt, D. H. 2003: Grimmiaceae. In: Gao, C., Crosby, M. R. & He, S. (eds.), Moss flora of China, vol. 3 [English version]: 3 76. Science Press, Beijing & Missouri Botanical Garden Press, St. Louis. Deguchi, H. 1978: A revision of the genera Grimmia, Schistidium and Coscinodon (Musci) of Japan. Journal of Science of the Hiroshima University, Series B 16: 121 256. Hastings, R. I. 1996: The genus Coscinodon (Bryopsida, Grimmiaceae) in South America, including a new species. The Bryologist 99: 418 427. Hastings, R. I. 2007: Coscinodon. In: Flora of North America Editorial Committee (ed.), Flora of North America North of Mexico, vol. 27: 258 262. Oxford University Press, New York. Hastings, R. I. & Greven, H. C. 2007: Grimmia. In: Flora of North America Editorial Committee (ed.), Flora of North America North of Mexico, vol. 27: 225 258. Oxford University Press, New York. Hernández-Maqueda, R., Quandt, D. & Muñoz, J. 2008a: Testing reticulation and adaptative convergence in the Grimmiaceae (Bryophyta). Taxon 57: 500 510. Hernández-Maqueda, R., Quandt, D., Werner, O. & Muñoz, J. 2008b: Phylogeny and classification of the Grimmiaceae/Ptychomitriaceae complex (Bryophyta) inferred from cpdna. Molecular Phylogenetics and Evolution 46: 863 877. Ignatova, E. A. & Muñoz, J. 2005: The genus Grimmia Hedw. (Grimmiaceae, Musci) in Russia. Arctoa 13: 101 182. Maier, E. 2002a: The genus Grimmia (Musci, Grimmiaceae) in the Himalaya. Candollea 57: 143 238. Maier, E. 2002b: Grimmia dissimulata E. Maier sp. nova,

238 Feng et al. Ann. BOT. Fennici Vol. 50 and the taxonomic position of Grimmia trichophylla var. meridionalis Müll. Hal. (Musci, Grimmiaceae). Candollea 56: 281 300. Maier, E. 2010: The genus Grimmia Hedw. (Grimmiaceae, Bryophyta): a morphological-anatomical study. Boissiera 63: 1 377. Maier, E. & Geissler, P. 1995: Grimmia in Mitteleuropa: Ein Bestimmungsschlüssel. Herzogia 11: 1 80. Muñoz, J. 1998: A taxonomic revision of Grimmia subgenus Orthogrimmia (Musci: Grimmiaceae). Annals of the Missouri Botanical Garden 85: 367 403. Muñoz, J. & Pando, F. 2000: A world synopsis of the genus Grimmia (Musci, Grimmiaceae). Monographs in Systematic Botany from the Missouri Botanical Garden 83: 1 133. Nyholm, E. 1998: Illustrated flora of Nordic mosses. Fasc. 4. Nordic Bryological Society, Copenhagen & Lund. Ochyra, R., Zarnowiec, J. & Bednarek-Ochyra, H. 2003: Census catalogue of Polish mosses. Polish Academy of Sciences, W. Szafer Institute of Botany, Kraków. This article is also available in pdf format at http://www.annbot.net