Epiphytic bryophytes are structural components in tropical and sub-tropical forests. To understand variation of the biomass of bole bryophytes along the latitudinal and altitudinal gradients, the biomass of bole bryophytes in tropical forests (Mengla), sub-tropical forests (Zhenyuan) and sub-alpine forests (Lijiang) in Yunnan, SW China were carried out. The results showed: (1) Biomass of bole bryophytes were significantly different along the latitudinal and altitudinal gradients. The lowest (0.53 g?400 cm-2) and the highest (3.57 g?400 cm-2) biomass occurred in the tropical forest of Mengla and the subalpine coniferous forest of Lijiang, respectively. (2) There was no dominant species shared among the three forests. (3) The biomass proportion of dominant component declined along the altitude gradients, they were 92.3% (Mengla), 75.6% (Zhenyuan) and 85.2% (Lijiang) of the total biomass. (4) Smooth mat, fan and turf were the dominant life-forms in tropical forests, sub-tropical evergreen broadleaved forests and sub-alpine coniferous forests, respectively. The results would provide preliminary insights on the structure, function and dynamics in the mountain forest ecosystems.
[1] 刘文耀. 林冠附生物在森林生态系统养分循环中的作用[J]. 生态学杂志, 2000,19(2): 30—35.
[2] Andrew N R, Rodgerson L, Dunlop M. Variation in invertebrate bryophyte community structure at different spatial scales along altitudinal gradients[J]. Journal of Biogeography, 2003,30(5): 731—746.
[3] 吴玉环,黄国宏,高谦,曹同. 苔藓植物对环境变化的响应及适应性研究进展[J]. 应用生态学报, 2001,12(6): 943—946.
[4] Ah-Peng C, Wilding N, Kluge J, Descamps-Julien B, Bardat J, Chuah-Petiot M, Strasberg D, Hedderson T A J. Bryophyte diversity and range size distribution along two altitudinal gradients: Continent vs. island[J]. Acta Oecologica, 2012,42: 58—65.
[5] 郭娜,刘剑秋. 植物生物量研究概述[J]. 亚热带植物科学, 2011,40(2): 83—88.
[6] Humphrey J W, Davey S, Peace A J, Ferris R, Harding K. Lichens and bryophyte communities of planted and semi-natural forests in Britain: the influence of site type, stand structure and dead wood[J]. Biological Conservation, 2002,107(2): 165—180.
[7] 马文章. 云南哀牢山徐家坝地区附生(植)物的组成、生物量及其与生态因子的关系[D]. 昆明: 中国科学院西双版纳热带植物园博士学位论文, 2009.
[8] 马文章,刘文耀,杨礼攀,杨国平. 边缘效应对山地湿性常绿阔叶林附生植物的影响[J]. 生物多样性, 2008,16(3): 245—254.
[9] 包维楷,雷波,冷俐. 六种人工针叶幼林下地表苔藓植物生物量与碳贮量[J]. 应用生态学报, 2005,16(10): 1817—1821.
[10] 王智慧,张朝晖. 贵州云台山喀斯特森林生态系统苔藓植物群落生物量研究[J]. 贵州师范大学学报(自然科学版), 2010,28(4): 88—91.
[11] Sun S Q, Wu Y H, Wang G X, Zhou J, Yu D, Bing H J, Luo J. Bryophyte species richness and composition along an altitudinal gradient in Gongga Mountain, China[J]. PLoS ONE, 2013,8(3): e58131.
[12] 叶吉,郝占庆,戴冠华. 长白山暗针叶林苔藓植物生物量的研究[J]. 应用生态学报, 2004,15(5): 737—740.
[13] 白学良,赵连梅,孙维,孙卫国. 贺兰山苔藓植物物种多样性、生物量及生态学作用的研究[J]. 内蒙古大学学报(自然科学版), 1998,27(1): 118—124.
[14] 刘俊华,包维楷. 冷杉天然林下地表主要苔藓斑块生物量及其影响因素[J]. 植物学通报, 2006,23(6): 684—690.
[15] Gradstein S R, Vanreenen G B A, Griffin D. Species richness and origin of the bryophyte flora of the Colombian Andes[J]. Acta Botanica Neerlandica, 1989,38(4): 439—448.
[16] Wolf J H D. Diversity patterns and biomass of epiphytic bryophytes and lichens along an altitudinal gradient in the northern Andes[J]. Annals of the Missouri Botanical Garden, 1993,80(4): 928—960.
[17] Song L, Ma W Z, Yao Y L, Liu W Y, Li S, Chen K, Lu H Z, Cao M, Sun Z H, Tan Z H, Nakamura A. Bole bryophyte diversity and distribution patterns along three altitudinal gradients in Yunnan, China[J]. Journal of Vegetation Science, 2015,26(3): 576—587.
[18] 童绍玉,陈永森. 云南坝子研究[M]. 昆明: 云南大学出版, 2007: 1—17.
[19] 高谦,曹同. 云南植物志(第17卷)[M]. 北京: 科学出版社, 2000.
[20] 黎兴江. 云南植物志(第18卷)[M]. 北京: 科学出版社, 2002.
[21] 黎兴江. 云南植物志(第19卷)[M]. 北京: 科学出版社, 2005.
[22] Bates J W. Is ‘life-form’ a useful concept in bryophyte ecology?[J]. Oikos, 1998,82(2): 223—237.
[23] Song L, Liu W Y, Ma W Z, Tan Z H. Bole epiphytic bryophytes on Lithocarpus xylocarpus (Kurz) Markgr. in the Ailao Mountains, SW China[J]. Ecological Research, 2011,26: 351—363.
[24] R Development Core Team. R: A language and environment for statistical computing. r foundation for statistical computing. Vienna, Austria, ISBN 3-900051-07-0, URL: http://www.R-project.org, 2007.
[25] Freiberg M, Freiberg E. Epiphyte diversity and biomass in the canopy of lowland and montane forest in Ecuador[J]. Journal of Tropical Ecology, 2000,16(5): 673—688.
[26] Schmitt C K, Slack N G. Host specificity of epiphytic lichens and bryophytes: A comparison of the Adirondack Mountains (New York) and the southern Blue Ridge Mountains (North Carolina)[J]. Bryologist, 1990,93(3): 257—274.
[27] Rabinowitz D. Seven forms of rarity[M]//Synge H. The biological aspects of rare plant conservation. Chichester: Wiley, 1981: 205—217.
[28] Gimingham C H, Birse E M. Ecological studies on growth-form in bryophytes: I. correlations between growth-form and habitat[J]. Journal of Ecology, 1957,45(2): 533—545.
[29] Song L, Zhang Y J, Chen X, Li S, Lu H Z, Wu C S, Tan Z H, Liu W Y, Shi X M. Water relations and gas exchange of fan bryophytes and their adaptations to microhabitats in an Asian subtropical montane cloud forest[J]. Journal of Plant Research, 2015,28(4): 573—584.
[30] 陈玉凯,杨琦,莫燕妮,杨小波,李东海,洪小江. 海南岛霸王岭国家重点保护植物的生态位研究[J]. 植物生态学报, 2014, 38(6): 576—584.
[31] 刘秀珍,张金屯. 天龙山植物群落优势种群生态位研究[J]. 山西大学学报(自然科学版), 2004,27(4): 418—423.