海南热带云雾林附生维管植物对宿主的选择性

附生维管植物是热带森林中重要的特征性组分, 研究附生维管植物对宿主树的选择性对热带森林生物多样性及生态系统保护有重要意义。该研究以海南热带雨林国家公园霸王岭片区热带云雾林中的附生维管植物为研究对象, 通过设置21个20 m × 20 m的固定样地, 调查样地内所有胸径>1 cm的乔、灌木的数量、种类、胸径、植株高、基质类型及其上生长的附生维管植物的数量、种类, 用混合线性模型、单因素方差、附生选择性指数分析附生维管植物分布与宿主树种、胸径、高度、基质类型(裸树皮、苔藓、凋落物及土壤)的关系。结果表明: 在热带云雾林8 400 m²样地内, 附生维管植物共计51种2 650株, 附生兰科植物和附生蕨类植物为优势类群, 附着在10.6%的个体木上; 附生维管植物多度和丰富度与宿主树胸径显著正相关; 多度较大的琼崖石韦(Pyrrosia eberhardtii)、流苏贝母兰(Coelogyne fimbriata)、阴石蕨(Davallia repens)、蔓九节(Psychotria serpens)对宿主树种表现出一定的选择性, 显著偏好1-4个树种; 附生维管植物对轻基质类型(苔藓植物)也存在显著偏好, 70%以上的附生维管植物生存在苔藓基质上。     

海南霸王岭不同森林类型附生兰科植物的多样性和分布

附生兰科植物是热带林附生植物的主要类群之一,对于维持热带林生态系统的物种多样性及生态功能具有重要的作用。以海南岛霸王岭国家级自然保护区内的6种热带原始林类型(热带季雨林、低地雨林、热带针叶林、山地雨林、山地常绿林及山顶矮林)中的附生兰科植物为研究对象,通过样带调查(每个森林类型设置12个10m×50m的样带,记录每个样带内胸径(DBH)≥5cm的树木及藤本上附生兰科植物的物种名称、株数及附生位置)分析了附生兰科植物的物种多样性、附生位置及其在不同森林类型中的分布规律。结果表明:1)3.6hm2森林调查样带内共记录到附生兰科植物9634株,分属于26属60种;2)除趋势对应分析(DCA)结果表明,6种森林类型中的附生兰科植物可分成5组(其中,山地常绿林与山顶矮林内的附生兰科植物归为一组);3)分布海拔范围相临近的森林类型的附生兰科植物具有较高的相似性,山地常绿林和山顶矮林附生兰科植物的相似性最高(88.9%);4)6种森林类型中,较高海拔的3种森林类型(山地雨林、山地常绿林和山顶矮林)中,附生兰科植物的丰富度和多度均显著高于其在较低海拔的3种森林类型(热带季雨林、低地雨林和热带针叶林),其中,附生兰科植物在山地常绿林内的丰富度和多度均最高;5)热带季雨林、低地雨林、热带针叶林及山地雨林内,宿主冠区附生兰科植物的多度均高于干区;山地常绿林内两者之间无显著差异;而山顶矮林干区的附生兰科植物的多度高于冠区;6)调查木上附生兰科植物的发生率在高海拔森林类型均高于其在低海拔森林类型,各森林类型内附生兰科植物的多度及物种丰富度与宿主胸径均存在显著正相关关系。     

不同微生境下季风常绿阔叶林附生维管植物多样性特征

附生植物是森林生态系统中的重要结构性成分,对于维持森林生态系统物种多样性及生态系统功能均具有重要意义。该研究对云南普洱市太阳河省级自然保护区内季风常绿阔叶林5种微生境(陡坡、缓坡、高谷、沟谷和山脊)的附生维管植物组成进行野外实地调查,并结合地形数据和其他环境数据,分析了附生维管植物的多样性及其与微生境的关系。结果表明：(1)研究区季风常绿阔叶林中共记录附生维管植物97种12 302株,分属16科45属;物种 多度曲线显示,隐柄尖嘴蕨(Belvisia henryi)、带状书带蕨(Vittaria doniana)、半圆盖阴石蕨(Humata platylepis)等3个物种优势明显。(2)山脊生境中附生维管植物具有更高的物种多样性和个体多度,而缓坡、沟谷生境中附生维管植物个体多度均较低。(3)在不同径级以及不同高度宿主之间的附生维管植物丰富度均具有显著差异(P<0.05),物种主要分布在中小径级宿主及林木树干中下部位。(4)影响附生维管植物物种丰富度、个体多度的主要环境变量为海拔高度、光照强度、温度;回归分析表明,附生维管植物物种丰富度与海拔高度呈线性正相关关系、与光照强度呈线性负相关关系;附生维管植物物种个体多度与光照强度呈线性负相关关系,与海拔高度和温度均呈线性正相关关系。     

西双版纳布龙自然保护区勐宋片区附生维管植物多样性与分布特征（英文）

利用地面观测和单绳上树法初次对布龙自然保护区勐宋片区开展的附生维管植物调查表明:1)在6个样地77株宿主上(共调查96株乔木,占地约0.2 ha),共有1 756株、丛个体,隶属14科47属103种;相比世界其他区域,物种丰富度处于旧世界热带水平区间,高于温带,但明显低于新世界热带水平;2)兰科植物为最丰富的类群(60%),其次为蕨类植物(24%),其他类群占16%;3)垂直分布特征研究表明,距地面10~15 m的中等高度带为物种最丰富的区间,约有51%的物种;0~5 m高度带为个体数量最多的区间,共有约24%个体,揭示了除中等高度带以外的另一个重要附生生境;4)常见的绞杀型榕属植物未见,而半附生植物密脉鹅掌柴(Schefflera elliptica)和多蕊木(Tupidanthus calyptratus)数量较多。     

西双版纳布龙自然保护区勐宋片区附生维管植物多样性与分布特征

利用地面观测和单绳上树法初次对布龙自然保护区勐宋片区开展的附生维管植物调查表明:1)在6个样地77株宿主上(共调查96株乔木,占地约0.2ha),共有1 756株、丛个体,隶属14科47属103种;相比世界其他区域,物种丰富度处于旧世界热带水平区间,高于温带,但明显低于新世界热带水平;2)兰科植物为最丰富的类群(60％),其次为蕨类植物(24％),其他类群占16％;3)垂直分布特征研究表明,距地面10～ 15 m的中等高度带为物种最丰富的区间,约有51％的物种;0～5m高度带为个体数量最多的区间,共有约24％个体,揭示了除中等高度带以外的另一个重要附生生境;4)常见的绞杀型榕属植物未见,而半附生植物密脉鹅掌柴(Schefflera elliptica)和多蕊木(Tupidanthus calyptratus)数量较多.     

西双版纳热带森林附生维管植物的物种多样性与区系特征

附生植物是山地森林生态系统中重要的结构性成分。因受林冠调查技术限制, 人们对林冠附生植物知之甚少。本文在前人有关西双版纳植物区系研究的基础上, 结合野外调查和标本资料, 对该地区附生植物的物种组成与分布进行了整理。结果表明, 西双版纳热带森林附生维管植物共有29科134属486种, 约占全部维管植物的11%。附生兰科是最丰富的类群(69属293种), 其中以石斛属(Dendrobium) (49种)和石豆兰属(Bulbophyllum) (48种)物种数最多。蕨类是仅次于兰科的附生类群(13科38属97种), 其中水龙骨科(51种)占附生蕨类总数的50%以上。基于生活史和养分来源的划分标准, 该地区48%的附生物种属于兼性附生, 其次是以兰科为主的专性附生(46%), 半附生仅占6%。从区系上看, 西双版纳附生植物属的分布具有明显的热带亚洲性质。附生植物主要分布于资源受限的林冠生境, 对环境变化极为敏感, 在人为干扰日益加剧的背景下, 这类植物正面临严重威胁。因此, 需要加强对西双版纳林冠亚系统的保护。     

中国森林附生维管植物多样性数据集

附生维管植物是热带、亚热带湿性山地森林植物群落中物种最为丰富的类群之一, 在维系森林生物多样性及生态系统功能与服务中发挥着重要作用, 然而附生维管植物调查相对困难, 在多样性调查和统计中往往被忽视, 迄今为止我国尚缺乏全国范围的森林附生维管植物名录。本项研究基于已公开发布的数据库, 搜集并整理了1982-2022年间的关于中国森林附生维管植物研究的文献书籍。首先, 提取文献资料中的有效信息, 依据物种2000中国节点的数据进行标准化校正, 整理出中国森林附生维管植物共计49科246属1,739种, 然后据此编写了相对准确、完整的中国森林附生维管植物物种名录。本名录作为我国第一个全国性森林附生维管植物名录, 可为森林生物多样性保护工作提供重要的数据支持, 并能为深入研究附生维管植物的进化生物学、生物地理学及宏观生态学等领域提供重要的基础信息。     

海南岛热带天然针叶林主要树种的空间格局及关联性

天然针叶林在热带地区虽较为少见, 但其对维持热带地区的生物多样性和生境异质性具有特殊意义。在我国热带天然针叶林集中分布面积最大的海南霸王岭林区, 作者选择伴生阔叶树种优势度不同的两种典型南亚松(Pinus latteri)天然林(简称纯林和混交林), 采用点格局法分析了其林冠层、亚林层和林下层主要树种的空间分布格局及其关联性。结果表明: (1)纯林中林冠层的南亚松主要为聚集分布, 混交林中在较小尺度上为聚集分布, 在较大尺度上为随机分布。(2)纯林中亚林层树种在较小尺度上为聚集分布, 在较大尺度上为随机分布, 在混交林中主要为聚集分布。(3)纯林中林下层树种主要呈现为随机分布, 而在混交林中主要为聚集分布。(4)随着尺度的增加, 林冠层与其他两个层次的树种, 在纯林中表现出从空间无关联到正关联的变化趋势, 而在混交林中则表现出从空间无关联到负关联的变化趋势。(5)亚林层与林下层树种在各个尺度上都表现为空间正关联。由此可见, 热带天然针叶林中优势种南亚松对伴生阔叶树种的分布格局具有重要影响。     

川西周公山柳杉人工林群落的边缘效应

为研究人工林群落的边缘效应特征, 本文以川西周公山森林公园的柳杉(Cryptomeria fortunei)人工林破碎化大斑块为对象, 以植株平均胸径、平均高度、平均密度、丰富度指数(D)和Shannon-Wiener指数(H)来综合衡量边缘效应深度。在实地踏查的基础上, 从林缘向林内(梯度1至梯度5)设置5条样带(宽度为10 m), 在每条样带中设置4个10 m × 10 m的小样方进行调查。结果表明: (1)从物种组成上看, 在总面积为2,000 m²的20个小样方中共记录到111个物种, 隶属于54科96属, 物种数从林缘至林内递减。(2)从群落结构上看, 乔木层的平均胸径从林缘至林内呈减小趋势, 平均密度则相反, 平均高度无显著变化; 灌木层的平均密度从林缘向林内减小, 平均高度无显著变化; 草本层的平均密度和平均高度均呈减小趋势。(3)从物种多样性上看, 总体上各层次的丰富度指数和Shannon-Wiener指数均从林缘向林内呈减小趋势, 其中灌木层和草本层的变化趋势最明显; 同时, 林内各梯度与梯度1 (林缘)的共有种和相似性系数从林缘向林内递减。(4)分析各项群落特征发现, 平均高度、平均密度和相似性系数的数值在梯度2向梯度3过渡时的起伏变化最明显, 推断本研究中柳杉人工林斑块的边缘深度可达林内20 m。     

云南哀牢山地区森林附生维管植物多样性及区系特征

附生植物作为山地森林生态系统中重要的结构性成分,在维持森林生态系统生物多样性格局、水分和养分循环等方面发挥着重要作用。本文通过野外调查、标本查阅并结合相关文献,对云南哀牢山地区附生维管植物物种组成及分布进行了系统研究。结果显示,哀牢山地区附生维管植物共有23科83属218种,其中附生蕨类和兰科植物最丰富。附生蕨类有34属93种,以附生-石生蕨类生活型占优势,其中水龙骨科17属62种,占附生蕨类的66.67%,瓦韦属(Lepisorus)和石韦属(Pyrrosia)分别有13种和10种。附生兰科植物有26属65种,其中石斛属(Dendrobium)和石豆兰属(Bulbophyllum)分别有12种和8种。该地区附生维管植物属的分布具有明显的热带性质并以热带亚洲分布居多。附生植物生长于生境因子变化剧烈、资源有限的林冠,对环境变化敏感,极易遭受破坏且破坏后难以恢复,不少附生植物具有很高的药用、观赏等价值。因此,应加强对附生维管植物这一特殊类群的保护。     

Vascular Epiphytes on Isolated Pasture Trees Along a Rainfall Gradient in the Lowlands of Panama

Secondary habitats are increasing in importance in tropical countries due to ongoing destruction of pristine vegetation. In spite of the magnitude of current changes, our understanding of their effects on nontrees (e.g., nonvascular or vascular epiphytes) is still very patchy, particularly in lowland habitats. Here, we report a study with isolated pasture trees in southwest Panama. The >800 studied trees, which belonged to >100 different species, harbored almost 27,000 epiphytes of 83 species. Orchidaceae was the most species‐rich family, with almost 60 percent of all species, while Bromeliaceae were most abundant. A rainfall gradient in the study region from ca 1000 to >3000 mm explained more of the variation in species abundance and richness than host characteristics (e.g., species identity, tree size). The unexpectedly large number of epiphytes in these pastures still represents a substantial change relative to a natural setting, which is suggested by a comparison with a forest inventory under similar climatic conditions. In pastures, species richness was lower as deduced from individual‐based rarefaction curves, a larger proportion of species and individuals showed crassulacean acid metabolism, and the relationship of epiphyte abundance/species richness and tree diameter was much less steep. Even the already reduced diversity, however, may be only transient in secondary habitats—the long‐term persistence of epiphyte populations in pastures is an open question and has to be addressed by repeated monitoring to fully evaluate the significance of pasture trees for the conservation of vascular epiphytes in tropical lowlands.     

Effect of Host Tree Traits on Epiphyte Diversity in Natural and Anthropogenic Habitats in Ecuador

Vascular epiphytes represent a highly diverse element of tropical rain forests, but they depend strongly on the structure and taxonomic composition of their tree communities. For conservation planning, it is therefore critical to understand the effect of host tree characteristics on epiphyte species richness in natural and anthropogenically transformed vegetation. Our study compares the effect of human land‐use on epiphyte diversity based on 220 study plots in a lowland rain forest and an Andean cloud forest in western Ecuador. We evaluate the relevance of host tree size and taxonomic identity for epiphyte species richness in contiguous primary forests, forest fragments, isolated remnant trees (IRTs), and secondary forests. At both study sites, epiphyte diversity was highest in primary forests, and it was lowest on IRTs and in secondary forests. Epiphyte species numbers of forest fragments were significantly reduced compared with the contiguous primary forest at the lowland study site, but not in the cloud forest area. Host tree size was a core predictor among secondary forests, but it had less significance within other habitat types. Taxonomic identity of the host trees also explained up to 61 percent of the variation in epiphyte diversity, especially for IRTs. The structural and taxonomic composition of the tree community in anthropogenically transformed habitat types proved to be fundamental to epiphyte diversity. This highlights the importance of deliberate selection of tree species for reforestation in conservation programs and the possible negative effects of selective logging in primary forests. Abstract in Spanish is available at http://www.blackwell‐synergy.com/loi/btp .     

Contribution of peeling host for epiphyte abundance in two tropical dry forests in the “El Cielo Biosphere Reserve”, Mexico

Host traits partly determine the abundance and species richness of epiphytes in tropical forests. It has been proposed that older trees with rough bark and evergreens often house more individuals and more epiphytic species than those with thin, smooth, and peeling bark, which harbor few epiphytes. We hypothesize (i) that epiphytes are more abundant and species-rich in the more shaded forest, which is related to bark roughness, and (ii) that epiphytes are distributed in the middle of the host, where microenvironmental conditions are more favorable to survival. We evaluated abundance, species richness, and vertical distribution of epiphytes in two tropical dry forests, according to the deciduousness and basal area of the trees. Moreover, we selected the most abundant epiphytes to test whether their distribution is related to a specific bark type and examine their vertical distribution in two dry forests. We distinguished a high abundance and species richness of epiphytes in the deciduous forest, although basal area and host species richness were higher in the semi-deciduous forest. In both forests, we found a positive relationship between epiphyte abundance and basal area. Higher abundance of epiphytes was related to the predominance of Tillandsia schiedeana, a drought-adapted species, in both forests. Unexpectedly, epiphytes abundantly colonized Bursera simaruba, a host with peeling bark and a very branched crown, where small individuals of T. schiedeana colonized abundantly toward the top of the crown. Our results show the importance of the tropical dry forest, particularly, B. simaruba, in maintaining epiphyte diversity in terms of T. schiedeana colonization.     

Long‐term changes of the vascular epiphyte assemblage on the palm Socratea exorrhiza in a lowland forest in Panama

Question: What are the qualitative and quantitative long‐term changes in the vascular epiphyte assemblage on a particular host tree species? Location: Lowland rain forest of the San Lorenzo Crane Plot, Republic of Panama. Methods: We followed the fate of the vascular epiphyte assemblage on 99 individuals of the palm Socratea exorrhiza by three censuses over the course of five years. Results: The composition of the epiphyte assemblage changed little during the course of the study. While the similarity of epiphyte vegetation decreased on individual palms through time, the similarity analysed over all palms increased. Even well established epiphyte individuals experienced high mortality with only 46% of the originally mapped individuals surviving the following five years. We found a positive correlation between host tree size and epiphyte richness and detected higher colonization rates of epiphytes per surface area on larger trees. Conclusions Epiphyte assemblages on individual S. exorrhiza trees were highly dynamic while the overall composition of the epiphyte vegetation on the host tree species in the study plot was stable. We suggest that higher recruitment rates, due to localized seed dispersal by already established epiphytes, on larger palms promote the colonization of epiphytes on larger palms. Given the known growth rates and mortality rates of the host tree species, the maximum time available for colonization and reproduction of epiphytes on a given tree is estimated to be ca. 60 years. This time frame will probably be too short to allow assemblages to be ever saturated.     

Host trait preferences and distribution of vascular epiphytes in a warm-temperate forest

To illustrate the ecological factors and process leading to the observed diversity patterns of vascular epiphytes, we examined the effect and importance of host tree traits on epiphyte richness and spatial aggregation of epiphytes. The study was conducted in warm-temperate forest in Japan. The recorded host traits were diameter, height, species, habitat topography, and growth rate, and we analyzed the effects and importance of these traits on three species groups: total epiphytic species, epiphytic orchid species, and epiphytic pteridophyte species. Diameter and species of host trees had the greatest influence on epiphytes and their magnitudes were roughly similar in all species groups. Growth rate and topography were less important than host size and species. Growth rate had a negative effect on all three groups, and topography was important for pteridophytes. Epiphyte richness did not exhibit clear spatial aggregation. Our results suggest that size, stability, and quality of the host are equally important in determining epiphyte colonization.     

A metapopulation approach to the analysis of long‐term changes in the epiphyte vegetation on the host tree Annona glabra

Question: Do vascular epiphyte species have a metapopulation structure? What are the qualitative and quantitative long‐term changes of the complete vascular epiphyte vegetation in a particular host tree species? Location: Lowland forest on Barro Colorado Island (9° 10’ N, 79°51’ W), Republic of Panama. Methods: In 1994 and 2002 we conducted a census of all vascular epiphytes growing on more than 1000 Annona glabra trees (= patches). Epiphyte species abundances were recorded at the tree level in each census. Results: The number of epiphyte individuals increased from ca. 15 000 to ca. 23 700 individuals during the census interval while the species composition on Annona glabra as a whole was rather stable. There was a strong positive relationship between occurrence in patches and local abundance of the species, and between species richness and host tree stand size. The dynamics of local populations of a given species were uncorrelated to each other; small and large local populations of most species had the same probability to go extinct. The frequency distribution of species on all host trees was not bimodal, but on a subset of heavily colonized host tree stands it was. Numbers of species and individuals were correlated with tree size which was not due to a correlation of tree size and tree age. Conclusions: As far as the most abundant epiphyte species with metapopulation structures are concerned, these species belong to diverse families, e. g. Orchidaceae, Bromeliaceae and Polypodiaceae. Even ca. 80 years after the initial establishment of the host tree species in the study area epiphytes are still in the stage of initial colonization and have not reached a steady state as indicated by the strong increase in individuals and the ongoing colonization of empty trees.     

Conservation of Vascular Epiphyte Diversity in Shade Cacao Plantations in the Chocó Region of Ecuador

To assess the contributions of rustic shade cacao plantations to vascular epiphyte conservation, we compared epiphyte species richness, abundance, composition, and vertical distributions on shade trees and in the understories of six plantations and adjacent natural forests. On three phorophytes and three 10 × 10 m understory plots in each of the agroforestry plantations and natural forests, 54 and 77 species were observed, respectively. Individual-based rarefaction curves revealed that epiphyte species richness was significantly higher on forest phorophytes than on cacao farm shade trees; detailed analyses showed that the differences were confined to the inner and outer crown zones of the phorophytes. No differences in epiphyte species richness were found in understories. Araceae, Piperaceae, and Pteridophyta were less species-rich in plantations than in forests, while there were no differences in Orchidaceae and Bromeliaceae. Regression analysis revealed that epiphyte species richness on trunks varied with canopy cover, while abundance was more closely related to soil pH, canopy cover, and phorophyte height. For crown epiphytes, phorophyte diameter at breast height (dbh) explained much of the variation in species richness and abundance. There were also pronounced downward shifts in the vertical distributions of epiphyte species in agroforests relative to natural forests. The results confirm that epiphyte diversity, composition, and vertical distributions are useful indicators of human disturbance and showed that while the studied plantations serve to preserve portions of epiphyte diversity in the landscape, their presence does not fully compensate for the loss of forests.     

The Conservation Value of Secondary Forests for Vascular Epiphytes in Central Panama

Secondary forests that develop following land abandonment could compensate for the losses of diversity and structure that accompany deforestation of old‐growth forests in tropical regions. Whether secondary forests can harbor similar species richness, density, and composition of old‐growth forests for vascular epiphytes remains largely unknown for secondary forests older than 50 yr. We examined community structure (species richness, density, and species composition) of vascular epiphytes in older secondary forests between 35 and 115 yr after land abandonment and nearby old‐growth forests to determine if the community structure of epiphytes in secondary forests approaches that of old‐growth forests over time. The recovery of epiphyte species richness was rapid with 55‐year‐old forests containing 65 percent of old‐growth epiphyte species richness. Secondary forest epiphyte communities were found to be statistically nested within secondary forests older in age and within old‐growth forests. Similarity of epiphyte communities to old‐growth forests increased to 75 percent, 115 yr after abandonment. This study suggests that secondary forests will likely recover old‐growth epiphyte richness and composition given enough time. Epiphyte densities did not recover quickly with 55‐year‐old forests having 14 percent and 115‐year‐old forests having only 49 percent of the density of old‐growth forest epiphytes. The low density of epiphytes in secondary forests could impact rainforest diversity and function. We conclude that in less than 115 yr, although secondary moist forests have high conservation value for some aspects of community structure, they are unlikely to compensate biologically for the loss of diversity and ecosystem function that high epiphyte densities provide.     

Do cloud forest tree species differ in their suitability as a substrate for epiphytic bromeliads?

There is evidence for the existence of varying degrees of host preference in vascular epiphytes; certain tree species can be positively, neutrally, or negatively associated with epiphytes. The objective of this study was to evaluate whether tree species of the cloud forest differ in their suitability as a substrate for epiphytic bromeliads. To evaluate the association between epiphytic bromeliad cover and host tree species, we sampled 62 plots (each of 200 m²) in four cloud forest fragments in Veracruz, Mexico. For all trees ≥10 cm in diameter at breast height (DBH), we recorded species name, DBH, and percentage cover of bromeliads in categories of tree coverage. In total, 587 trees belonging to 52 species were recorded. All of the 10 tree species used to assess differences in epiphyte cover (each with a minimum of nine individuals) supported bromeliads, but mean bromeliad cover differed significantly among the tree species. The tree species that concentrated the highest bromeliad cover were Quercus sartorii (29.86%) and Liquidambar styraciflua (21.72%). Our results indicate that, while none of the tree species analyzed was a limiting host for epiphytic bromeliads in general, varying levels of bromeliad cover occur depending on the host species in tropical montane cloud forest fragments suggesting that certain tree species are better hosts than others. The implications for conservation efforts of differential tree species suitability as epiphyte hosts are discussed.     

The relationship between tree size and epiphyte species richness: testing four different hypotheses

Aim For epiphytic plants trees are habitat units, and tree size determines epiphyte species richness. While growing, trees generate vertical microhabitats that are exploited by epiphytes. One would expect to find four different types of relationship between tree size and epiphyte species richness: positive linear (young trees), neutral (old trees), negative (old decaying trees) and positive asymptotic (trees of mixed size class in a mature forest). We tested these relationships in plots of colonizing sweetgum trees in pastureland, isolated remnant trees in pastureland (old oaks) and sweetgum and oaks in a pristine forest. Location The study was carried out in a landscape shaped by the fragmentation of lower montane cloud forest in San Andrés Tlalnelhuayocan (19°30′56′′ N and 96°59′50′′ W; 1500–1600 m a.s.l.) in central Veracruz, Mexico. Methods We measured the d.b.h. of all oaks and sweetgum trees (d.b.h. ≥ 5 cm) present in pastureland and in three 100 m² plots of a lower montane cloud forest. All trees were climbed and species richness of the epiphytes recorded. Results As expected, colonizer trees in pastureland showed a linear positive relationship. Although we found evidence that remnant oaks in pastureland had a neutral relationship between tree size and epiphyte species richness, the low power of the test did not allow us to make conclusions about the kind of relationship. Mixed size‐class pristine forest trees showed a positive linear relationship between tree size and epiphyte species richness instead of a positive asymptotic one. Main conclusions Our results suggest that in the study area epiphyte communities are unsaturated, as the number of species increases with tree size and does not reach a ceiling. This evidence supports the idea that the species–area relationship is not asymptotic. However, the epiphyte community on remnant pastureland oaks may be saturated as epiphyte species richness did not increase with tree size, but a larger sample size is needed to confirm the neutral pattern. Neutral, asymptotic and negative patterns in the relationship between tree size and epiphyte species richness depend on the saturation of the trees by epiphytes. Other studies have suggested tree saturation, but further research is necessary in order to confirm or rule out these patterns.