亚热带常绿阔叶林林分结构对物种组成变异的驱动作用: 从局域到区域尺度
Driving effects of forest stand structure of a subtropical evergreen broad-leaved forest on species composition variation: From local to regional scales
通讯作者: *E-mail:tan@ynu.edu.cn;linluxa@xtbg.ac.cn
编委: 储诚进
责任编辑: 黄祥忠
收稿日期: 2022-03-29 接受日期: 2022-05-25
基金资助: |
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Corresponding authors: *E-mail:tan@ynu.edu.cn;linluxa@xtbg.ac.cn
Received: 2022-03-29 Accepted: 2022-05-25
林分结构可以表征森林群落光的可利用性和光环境的异质性, 对群落物种组成的变异具有重要驱动作用。然而, 目前还鲜有研究将林分结构用于解释群落物种组成的变异。本研究以哀牢山亚热带中山湿性常绿阔叶林20 ha森林动态监测样地及其周边区域按公里网格设置的19个1 ha森林动态样地为研究对象, 将林分结构参数、环境因子和空间结构变量共同作为解释变量, 采用基于冗余分析的变差分解和层次分割方法, 在局域和区域尺度上同时解析群落物种组成变异的驱动因素。结果表明, 在局域和区域尺度上, 纳入林分结构后均提高了对物种组成变异的解释率。在局域尺度上, 加入林分结构作为解释变量后, 单纯的空间结构的解释率明显下降, 林分结构与环境因子累计贡献了41.0%的解释率。在区域尺度上, 林分结构与环境因子累计贡献了23.0%的解释率。从局域到区域尺度, 环境过滤的相对作用明显增强。林分结构指示的光的可利用性对林冠下方的树种组成具有较强的塑造作用, 今后的研究应进一步探讨林分结构对亚热带常绿阔叶林物种组成变异的驱动机制。
关键词:
Aim: The variation of species composition can be partitioned into two components which are explained by environment and space, and can be used to further explore the niche process and neutral process of community assembly. Forest stand structure characterizes the light availability and heterogeneity under forest canopies, and it is a major driving factor in the variation of species composition for forest communities. However, few studies have applied forest stand structure to explain the variation of species composition within forest communities. In this study, we sampled 19 separate 1-ha forest dynamics plots established among grids of 1 km2 (regional scale) near the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot (local scale, less than 1 km2) in Ailao Mountains as a research platform. Using forest stand structure, environmental factors, and spatial structure variables as the explanatory variables for the species composition variation. We resolved the driving forces of species composition variation at local and regional scales, with an emphasis on the role of forest stand structure in driving the variation of species composition.
Methods: Based on a long-term community survey and airborne LiDAR data, we used redundancy analysis (RDA) and variance partitioning to analyze how environment, spatial structure, and forest stand structure were related to species composition variation in a subtropical evergreen broad-leaved forest at both local and regional scales. To explore the main factors driving the variation of species composition, we analyzed the relative importance of individual explanatory variables using commonality analysis and hierarchical partitioning method.
Results: Inclusion of forest stand structure as an explanatory variable increased the response rate of the variation of species composition at both local and regional scales. However, inclusion of forest stand structure as an explanatory variable resulted in a significant decrease in the rate of spatial structure at the local level. The cumulative contribution of forest stand structure and environment to the variation in species composition was 41.0% at the local level. At the regional scale, forest stand structure and environment contributed a cumulative explanatory rate in species composition was 23.0%.
Conclusions: This study confirms that, for subtropical broad-leaved evergreen forests, forest stand structure characterizing the light environment is an important driver of the variation in species composition, which deepens our understanding of the role of environmental filtering in driving the variation in species composition and remedies the traditional under-consideration of environmental factors. From local to regional scales, the role of purely spatial structure declines sharply to negligible levels. However, the relative importance of environmental filtering is significantly enhanced from the local to the regional scale. Light availability may have a strong effect shaping species composition below the forest canopies. This new relationship between forest stand structure on species composition warrants future studies to explore the causal mechanisms of how forest stand structure drives species composition variation in subtropical broad-leaved evergreen forests.
Keywords:
本文引用格式
杨欣, 姚志良, 王彬, 温韩东, 邓云, 曹敏, 张志明, 谭正洪, 林露湘 (2023)
Xin Yang, Zhiliang Yao, Bin Wang, Handong Wen, Yun Deng, Min Cao, Zhiming Zhang, Zhenghong Tan, Luxiang Lin (2023)
驱动群落物种组成空间变化的生态过程是生态学研究的热点之一(Hubbell, 2001; Vellend, 2010; Page & Shanker, 2018)。生态学家通常将群落物种组成的变异划分为由环境和空间结构变量所解释的两个组分, 并进一步探讨环境过滤等生态过程在群落构建中的相对作用(Gilbert & Lechowicz, 2004; Chang et al, 2013)。环境对物种分布的调控, 即环境过滤, 反映在物种组成变化中由环境变量解释的组分(Whittaker, 1956; Gentry, 1988; Legendre et al, 2005; Chang et al, 2013), 而扩散限制等是塑造群落物种组成空间结构的生态过程, 其影响反映在物种组成变化中由空间变量解释的组分(Chave & Leigh, 2002; Condit et al, 2002; Gilbert & Lechowicz, 2004; Legendre et al, 2009)。解析群落物种组成变异驱动因素的相对作用有助于理解驱动群落构建的生态位与中性机制(Dray et al, 2012)。
已有研究普遍认为, 群落物种组成是由环境过滤和扩散限制等生态过程共同驱动的(Gilbert & Lechowicz, 2004; Gravel et al, 2006; Qian & Ricklefs, 2007; Legendre et al, 2009)。近年来的研究重点是解析环境过滤与扩散限制之间的相对重要性(Page & Shanker, 2018), 而这两类生态过程的相对重要性在不同生态系统或研究尺度上具有很大的差异(Qian & Ricklefs, 2007; 陈圣宾等, 2010; Myers et al, 2013)。例如, Myers等(2013)发现热带森林的物种组成差异主要受扩散限制驱动, 而在温带森林中, 环境过滤是最重要的驱动力。局域植物群落组成既取决于环境因子的异质性(如气候、土壤和地形条件等), 又受群落内生物间的相互作用及不同物种扩散能力强弱的影响(Levine & Murrell, 2003; Seidler & Plotkin, 2006; 牛克昌等, 2009; Chase & Myers, 2011)。在区域尺度上, 受地史过程和区域过程的影响, 不同区域之间的物种库存在差异, 会导致区域间物种组成的差异(方精云等, 2009), 并且区域间物种组成还受环境因子(特别是气候变化)的显著影响(Tuomisto et al, 2003; Toledo et al, 2011)。已有研究发现, 在局域尺度上, 物种组成相似性与地理距离之间存在较强的相关性, 表明物种分布受到扩散限制的影响; 而随着空间尺度的增大, 生态位分化可能是物种组成变化更重要的驱动因素(Page & Shanker, 2018)。局域群落物种共存格局的形成和维持不仅受局域生态过程的驱动, 同样也受区域生态过程(如种群扩散)的驱动(Ricklefs, 1987; Laliberté et al, 2009), 局域和区域过程共同作用于群落的结构和物种组成, 并且二者的相对作用大小随着群落和环境条件的不同而有差异(方精云等, 2009)。然而, 局域与区域尺度上, 不同生态过程相对重要性是否具有差异以及差异性如何, 还有待进一步研究和探讨。目前仍鲜有研究针对同一生态系统, 同时从局域和区域两个尺度上去解析不同生态过程在驱动群落物种组成变异中的相对作用, 这也进一步制约了对不同生态过程在局域和区域尺度上差异性的认知。
林冠结构的三维特征决定了森林群落中光的空间分布, 并进一步影响森林群落的生物多样性(Ishii et al, 2004)。林分结构在生物多样性格局形成中的作用已经得到越来越多的证实(周昌艳等, 2020; Thom et al, 2021; Zhang et al, 2022)。传统地面调查数据获取的林分结构主要是与胸径和个体数相关的参数, 难以直接反映林冠结构, 而激光雷达(light detection and ranging, LiDAR)遥感已被证明是定量化各类森林林冠结构的有效工具(Lefsky et al, 2002; Drake et al, 2003; 郭庆华等, 2020; Zhang et al, 2022)。基于激光雷达获取的林冠结构参数是一种对传统林分结构参数的重要补充, 并在解释生物多样性格局形成机制中发挥着重要作用(周昌艳等, 2020)。相较以往基于地面调查数据计算的相关林分结构参数, 通过激光雷达采集的点云数据计算的基于林冠结构的关键林分结构参数, 能够更好地反映群落中光的可利用性和光环境的异质性, 在解释物种组成变异中具有很大潜力。
以往对局域与区域尺度上不同生态过程相对重要性的认识, 通常是基于来自不同生态系统类型的研究, 同一生态过程对物种组成变异的驱动作用在局域与区域尺度上的差异, 需要针对同一生态系统来比较才能得到客观的认知。我们预测, 从局域尺度到区域尺度, 环境过滤的相对作用明显增强, 表征光环境的林分结构将进一步提高环境过滤的解释率。本研究以哀牢山亚热带常绿阔叶林为研究对象, 基于局域尺度的哀牢山亚热带中山湿性常绿阔叶林20 ha动态样地, 以及其周边区域尺度上按公里网格布设的19个1 ha森林动态样地, 同时从局域与区域两个尺度对物种组成变化的驱动因素进行解析, 将林分结构参数、环境因子、空间结构变量共同作为物种组成变异的解释变量, 通过冗余分析和变差分解的方法, 解析不同生态过程的相对作用及其在局域和区域尺度上的差异。
1 材料与方法
1.1 研究区概况
研究区域位于云南省哀牢山国家级自然保护区, 保护区内分布着大片连续的亚热带常绿阔叶林。亚热带常绿阔叶林为云南的优势植被类型之一, 中山湿性常绿阔叶林是云南亚热带常绿阔叶林植被型下的一种植被亚型(朱华, 2021)。
1.2 样地设置
本研究以中国科学院亚热带森林生态系统研究站建立和管理的哀牢山中山湿性常绿阔叶林20 ha动态样地(简称哀牢山大样地)及其周边按公里网格设置的19个1 ha森林动态样地为研究平台。
哀牢山大样地位于哀牢山国家级自然保护区内(101°01′ E, 24°32′ N), 于2014年建成。样地投影面积为20 ha (500 m × 400 m), X轴指向为南偏东6.37° (温韩东等, 2018; 姚志良等, 2020)。样地内平均海拔为2,523 m, 10 m桩的最低海拔为2,472 m, 最高海拔为2,628 m, 海拔高差156 m。哀牢山大样地的建设参照Center for Tropical Forest Science (CTFS)的建设标准(Condit et al, 1998)。用全站仪将样地划分为500个20 m × 20 m的样方和8,000个5 m × 5 m的小样方, 对其中所有胸径(diameter at breast height, DBH) ≥ 1 cm的木本植物(不包括藤本和竹类植物)个体及其分枝进行挂牌标记、物种鉴定, 并测量胸径及空间坐标, 记录生长状态等。
于2018年在哀牢山大样地周边区域按公里网格布设了19个1 ha森林动态样地(简称公里网格样地), 每个1 ha样地的森林群落类型是该公里网格内的主体森林群落类型。哀牢山公里网格样地分布范围为101°00′-101°02′ E, 24°30′-24°34′ N。公里网格样地同样遵循CTFS的标准, 用全站仪将每个样地划分为25个20 m × 20 m的样方和100个10 m × 10 m的小样方。对小样方内所有DBH ≥ 10 cm的木本植物(不包括藤本和竹类植物)个体及其分枝进行挂牌标记、物种鉴定, 并测量胸径及空间坐标, 记录生长状态等。
本研究以哀牢山大样地及公里网格样地的树种(DBH ≥ 10 cm)为研究对象, 以1 ha样地为分析单元, 分别以局域尺度上的哀牢山大样地(划分成20个1 ha样地)和区域尺度上的公里网格样地(19个1 ha样地)为分析尺度。
1.3 环境因子
在样地内10 m桩位置利用全站仪测得相对高差, 再根据实时差分定位(real-time kinematic, RTK)实测的四角坐标的海拔值进行校正, 得到所有10 m桩的海拔值。基于10 m桩海拔数据计算海拔范围(Yu et al, 2015)、平均海拔、海拔标准差(Brown et al, 2013)、海拔峰度、海拔偏度、坡度范围、坡度标准差(Yu et al, 2015)、坡向正弦值标准差、坡向余弦值标准差、凹凸度标准差、地形起伏度(Yu et al, 2015)和太阳辐射值共12个环境因子, 其中, 太阳辐射通过数字高程模型(digital elevation models, DEM)的结果利用ArcGIS 10.3中的“空间分析”工具计算。
1.4 空间结构
1.5 林分结构
以往基于清查数据获取的林分结构主要是与胸径相关的胸径变异系数、胸高断面积和等, 所反映的森林整体结构有限, 特别是不能直接反映垂直层面上的林分结构, 对光的可利用性和异质性的反映也十分有限。本研究于2018年10月至2019年2月, 使用DJI M600 Pro六旋翼电动无人机搭载Velodyne LiDAR PUCK-16激光雷达传感器, 采集三维点云数据。为避免边缘畸变, 采集点云数据过程中, 均在样地边缘适当扩飞。设置无人机飞行高度为距冠层70 m, 以3.6 m/s的速度飞行, 旁向重叠率大于70%, 点云剖面见附录1。
本研究的林分结构参数包括了传统的基于清查数据计算的胸径变异系数和胸高断面积和, 同时增加基于机载激光雷达获取的林分结构参数。激光雷达获取的林分结构数据的提取主要基于LiDAR360 version 3.0软件, 通过无人机载激光雷达获取的三维点云数据计算与林冠相关的林分结构参数, 各个参数的具体描述参见附录2。
1.6 局域和区域尺度上物种组成相似性的距离衰减
1.7 基于冗余分析的变差分解
以环境因子的前3个主成分、林分结构参数的前2个主成分和前向选择后的空间结构变量为解释变量。为避免林分结构解释变量包含冠层个体(林分结构的主要塑造者)的物种组成变异, 去除了胸径在90%分位数以上的冠层个体, 以经Hellinger转化的样地 × 物种的多度矩阵为响应变量, 通过R软件中的vegan包进行冗余分析和变差分解(Oksanen et al, 2020)。为揭示林分结构在驱动物种组成变异中的作用, 本研究在局域和区域两个尺度上分别进行两次变差分解, 第一次只纳入环境因子和空间结构变量, 第二次纳入环境因子、空间结构变量和林分结构变量。
1.8 通过层次分割解析单个解释变量的相对重要性
2 结果
2.1 物种组成
哀牢山大样地于2019年完成第一次复查工作。基于复查数据, 胸径在10 cm以上的个体属于74个物种(包括1个未知物种), 已鉴定的73个物种属于23科43属(附录5)。哀牢山公里网格样地胸径在10 cm 以上的个体属于83个物种(包括2个未知物种), 已鉴定的81个物种属于24科48属(附录6)。其中, 仅在大样地出现的物种有13个, 仅在公里网格样地出现的物种有21个。
构成哀牢山大样地的20个1 ha样地, 其物种丰富度变化范围为30-44个树种, 多度为472-1,339个个体(附录7)。19个1 ha公里网格样地的物种丰富度为28-44个树种, 多度为384-1,073个个体(附录8)。在局域和区域两个尺度上, 样地间的物种组成相似性均表现出随样地间距离增大而降低的趋势(图1)。基于公里网格样地可见光近地面遥感正射影像识别了19个1 ha样地的冠层个体(附录8), 其相对多度仅为6.0%-13.1%, 群落组成的变化主要为林冠以下的个体所贡献。
图1
图1
样地间物种组成相似性的距离衰减图。(a)由哀牢山亚热带中山湿性常绿阔叶林20 ha森林动态样地划分成的20个1 ha样地; (b)哀牢山20 ha样地周围按公里网格设置的19个1 ha森林动态样地。
Fig. 1
Distance decay of species compositional similarity between plots. (a) 20 1-ha plots divided by the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot in Ailao Mountains; (b) 19 1-ha forest dynamics plots established among grids of 1 km2 near the 20 ha forest dynamics plot in Ailao Mountains.
2.2 环境因子和空间结构在局域和区域尺度上对群落物种组成变异的相对贡献
变差分解结果表明, 哀牢山大样地单纯的空间结构和单纯的环境因子分别解释了群落物种组成变异的47.2%和7.1%, 二者共同解释了8.3%, 未解释部分为37.5%, 即单纯的空间结构解释了哀牢山大样地群落物种组成47.2%的变异, 而单纯的环境因子与环境的空间结构的联合效应仅解释了群落物种组成15.4 %的变异(图2a)。相比之下, 哀牢山公里网格样地单纯的空间结构解释率为1.4%, 单纯的环境因子解释了4.2%, 二者共同解释了7.1%, 未解释部分为87.3%, 即单纯的空间结构仅能解释哀牢山公里网格样地物种组成变异的1.4%, 单纯的环境因子与环境的空间结构的联合效应可解释11.3% (图2b)。
图2
图2
由哀牢山亚热带中山湿性常绿阔叶林20 ha森林动态样地划分成的20个1 ha样地和哀牢山20 ha样地周围按公里网格设置的19个1 ha森林动态样地的空间结构、环境因子变差分解(a、b)及空间结构、环境因子和林分结构变差分解(c、d) Venn图(< 0的部分不显示)
Fig. 2
The Venn diagram of variation partitioning explained by spatial structures and environmental factors (a, b) and by spatial structures, environmental factors and forest stand structures (c, d) of 20 1-ha plots divided by the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot in Ailao Mountains and 19 1-ha forest dynamics plots established among grids of 1 km2 near the 20 ha forest dynamics plot in Ailao Mountains (values < 0 not shown)
2.3 林分结构、环境和空间结构在局域和区域尺度上对群落物种组成变化的相对贡献
图3
图3
通过rdaca.hp解析由哀牢山亚热带中山湿性常绿阔叶林20 ha森林动态样地划分成的20个1 ha样地空间结构、环境因子和林分结构各变量的相对重要性。FS_PC1、FS_PC2分别代表林分结构的第一主成分和第二主成分; Env_PC1、Env_PC2、Env_PC3分别代表地形环境因子的第一至第三主成分; MEM3、MEM4、MEM5、MEM6、MEM8、x、y代表空间结构, 其中, x和y为空间结构的线性趋势。
Fig. 3
The relative importance of individual variables of spatial structures, environmental factors and forest stand structures in 20 1-ha plots divided by the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot in Ailao Mountains by rdacca.hp. FS_PC1 and FS_PC2 represent the first and the second principal components of forest stand structures, respectively. Env_PC1, Env_PC2 and Env_PC3 represent the first, the second and the third principal components of topographic environmental factors, respectively. MEM3, MEM4, MEM5, MEM6, MEM8, x and y represent the spatial structures, where, x and y are linear trends of spatial structures.
图4
图4
通过rdaca.hp解析哀牢山20 ha森林动态样地周围按公里网格设置的19个1 ha森林动态样地空间结构、环境因子和林分结构各变量的相对重要性。FS_PC1、FS_PC2分别代表林分结构的第一主成分和第二主成分; Env_PC1、Env_PC2、Env_PC3分别代表地形环境因子的第一至第三主成分; MEM1代表空间结构。
Fig. 4
The relative importance of individual variables of spatial structures, environmental factors and forest stand structures in 19 1 ha forest dynamics plots established among grids of 1 km2 near the 20 ha forest dynamics plot in Ailao Mountains by rdacca.hp. FS_PC1 and FS_PC2 represent the first and the second principal components of forest stand structures, respectively. Env_PC1, Env_PC2 and Env_PC3 represent the first, the second and the third principal components of environmental factors, respectively. MEM1 represents the spatial structures.
3 讨论
未加入林分结构时, 局域尺度上物种组成的绝大部分变异由单纯的空间结构(解释率为47.2%)驱动, 这可能是由于扩散限制产生了独立于环境变化的空间自相关结构(De Cáceres et al, 2012)。单纯的空间结构除了能在一定程度上反映中性过程外, 还可能包含一些未测量环境变量的空间结构(Legendre et al, 2009; Dray et al, 2012)。而区域尺度上, 物种组成的绝大部分变异来自环境因子及环境因子的空间结构(解释率为11.3%), 支持生态位理论的环境控制假说, 即物种通过环境过滤这一确定性过程而被选择进入群落(Page & Shanker, 2018)。未考虑林分结构作为解释变量之前, 局域和区域尺度上的结果与之前的研究结果类似(Page & Shanker, 2018)。然而, 环境过滤的存在并不与中性过程发生矛盾(Legendre et al, 2005), 重点在于检验这两个过程在驱动不同群落物种组成变异中的相对重要性(陈圣宾等, 2010; Page & Shanker, 2018)。
对于环境因子, 与很多基于大型森林动态样地的研究相同, 本研究采用的主要是易于获得的地形数据(Legendre et al, 2009; De Cáceres et al, 2012), 但地形不是光或温度等直接的环境变量(De Cáceres et al, 2012), 而是代表土壤湿度和小气候条件的一个间接变量, 综合表征了生境的整体质量(Legendre et al, 2009; Dray et al, 2012)。与环境因子有关的部分空间结构可以通过地形变量反映出来, 但不一定全部反映出来, 一些未观测的具有空间结构的环境变量和群落动态的空间结构效应都可能影响单纯的空间结构部分(Jones et al, 2008; Legendre et al, 2009)。而已有研究指出, 增加土壤数据作为环境因子将可能改变生态位过程和中性过程对群落物种组成变异的相对重要性(Chang et al, 2013)。因此, 在之后的研究中可以考虑测量土壤变量, 将其纳入环境因子进行分析。值得注意的是, 本研究针对的是胸径在10 cm以上的树种, 而中性过程对于小径级树种作用更大(Asefa et al, 2019), 如果考虑更多小径级树种, 环境过滤和中性过程的相对重要性结果也可能不同。
加入表征光环境的林分结构后, 将进一步加强对环境过滤的解析。在局域尺度上, 林分结构与环境因子累计贡献了41.0%的解释率, 在区域尺度上, 林分结构与环境因子累计贡献了23.0%的解释率, 局域和区域尺度均表现为环境过滤占主导。从局域到区域尺度, 单纯的空间结构解释率急剧下降至可以忽略的程度, 环境过滤作用也有明显下降, 这主要是因为局域尺度更容易受随机过程的影响, 而区域尺度则是确定性过程占主导(Ruokolainen et al, 2009; Page & Shanker, 2018)。然而, 从局域到区域尺度, 相对于空间结构, 环境过滤的重要性则明显增强, 这表明加入表征光环境的林分结构参数可以更好地解析环境过滤的相对重要性。采用层次分割法可以有效解析出具共线性的解释变量的相对重要性, 在局域和区域尺度, 指示光的可利用性的林分结构第一主成分对物种组成变异的解释率排名在前两位, 进一步说明林分结构在群落物种组成变异中具有重要作用。
林分结构的加入进一步填补了空间结构和环境因子中未解释的部分, 并且将原本被认为是环境或是空间单独解释的部分, 解析为与林分结构共同解释的部分, 这反映了林分结构所表征的光环境具有明显的过滤作用, 并且林分结构仍然是一种具有空间结构的环境因子。冠层可以截取进入森林群落的光(Binkley et al, 2010; Ali, 2019), 不同的冠层结构调控着林下光的可利用性, 通过不同的遮阴效应影响着冠层以下个体的物种组成(Matsuo et al, 2021), 进而驱动群落物种组成的变异。以往的研究也发现林分结构与物种组成具有较强的相关性(Hardiman et al, 2011; Fotis et al, 2018; Zhang et al, 2022)。因此, 冠层下方光的可利用性和光环境的异质性调控着除冠层个体以外的群落物种组成变异格局(Tateno & Takeda, 2003; Meyer et al, 2019; Yi et al, 2022)。另外, 林分结构会受地形因子的影响, 从而产生林分结构与环境因子的共同解释部分。而且林分结构除了表征林下光环境, 也可能表征土壤水分和其他营养物质(Zhang et al, 2015)。
区域尺度物种组成的未解释部分比较高, 可能是公里网格样地涉及部分山顶苔藓矮林, 物种组成相对大样地更为复杂, 环境异质性也更高。纳入林分结构参数后, 区域尺度物种组成解释率提高了10.8%, 但仍有相当一部分的变异未被解释(76.5%), 这可能是由于本研究纳入分析的环境因子和林分结构参数未能成功解析群落组成背后的生态过程, 推测可能一些本研究未考虑的生态学过程(如物种间的相互作用、生态漂变等)是导致群落物种组成差异的潜在驱动力(牛克昌等, 2009), 这部分也可能包含了随机过程, 或是一些本研究中未观测到的非空间结构属性的生物与非生物因子未纳入考虑(De Cáceres et al, 2012; Chang et al, 2013)。
不论是否考虑林分结构作为解释变量, 单纯的空间结构对区域尺度物种组成变异的解释率都较低, 但这并不代表区域尺度不存在扩散限制, 可能是我们采用的空间结构变量无法解释区域尺度扩散限制所产生的空间结构。本研究中区域尺度上的样地之间相距较远, 最近为430 m, 最远为6,647 m, 群落物种组成的空间自相关较弱, 因此本研究所采用的主要解释空间自相关的空间结构变量对区域尺度物种组成变异的解释率较低。物种组成相似性的距离衰减曲线可以证明区域尺度也存在扩散限制, 从而导致物种组成相似性随空间距离增加而降低的趋势。由于扩散限制和环境过滤之间的相互作用过于复杂, 而变差分解的方法存在一定缺陷, 可能无法完全解析二者的相对重要性(Smith & Lundholm, 2010)。
本研究针对同一类森林生态系统, 即亚热带中山湿性常绿阔叶林, 分别从局域和区域尺度解析环境、空间和林分结构对物种组成变异的驱动效应, 发现表征光的可利用性的林分结构对调控物种组成具有重要作用, 今后的研究应进一步探讨林分结构通过调控光环境进而驱动物种组成变异的机制。
附录 Supplementary Material
附录1 哀牢山样地机载激光雷达点云剖面示意图
Appendix 1 Diagram of airborne lidar point clouds profile in Ailao Mountain plots
附录2 本研究测定的林分结构参数基本信息
Appendix 2 Basic information on the parameters of forest stand structure measured in this study
附录3 由哀牢山亚热带中山湿性常绿阔叶林20 ha森林动态样地划分成的20个1 ha样地林分结构参数在前两个主成分上的载荷
Appendix 3 Loadings of forest stand structural parameters on the first two principal components in the 20 1-ha plots divided by the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot in Ailao Mountains
附录4 哀牢山20 ha动态样地周围按公里网格设置的19个1 ha森林动态样地林分结构参数在前两个主成分上的载荷
Appendix 4 Loadings of forest stand structural parameters on the first two principal components in 19 1-ha forest dynamics plots established among grids of 1 km2 near the 20 ha forest dynamics plot in Ailao Mountains
附录5 由哀牢山亚热带中山湿性常绿阔叶林20 ha森林动态样地划分成的20个1 ha样地树种名录
Appendix 5 Tree species list of the 20 1-ha plots divided by the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot in Ailao Mountains
附录6 哀牢山20 ha动态样地周围按公里网格设置的19个1 ha森林动态样地树种名录
Appendix 6 Tree species list of 19 1-ha forest dynamics plots established among grids of 1 km2 near the 20 ha forest dynamics plot in Ailao Mountains
附录7 由哀牢山亚热带中山湿性常绿阔叶林20 ha森林动态样地划分成的20个1 ha样地群落组成
Appendix 7 Community composition of 20 1-ha plots divided by the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot in Ailao Mountains
附录8 哀牢山20 ha动态样地周围按公里网格设置的19个1 ha森林动态样地群落组成
Appendix 8 Community composition of 19 1-ha forest dynamics plots established among grids of 1 km2 near the 20 ha forest dynamics plot in Ailao Mountains
参考文献
Forest stand structure and functioning: Current knowledge and future challenges
DOI:10.1016/j.ecolind.2018.11.017 URL [本文引用: 1]
Contrasting effects of space and environment on functional and phylogenetic dissimilarity in a tropical forest
DOI:10.1093/jpe/rty026 URL [本文引用: 1]
betapart: An R package for the study of beta diversity
DOI:10.1111/j.2041-210X.2012.00224.x URL [本文引用: 1]
Explaining growth of individual trees: Light interception and efficiency of light use by Eucalyptus at four sites in Brazil
DOI:10.1016/j.foreco.2009.05.037 URL [本文引用: 1]
Forward selection of explanatory variables
DOI:10.1890/07-0986.1
PMID:18831183
[本文引用: 1]
This paper proposes a new way of using forward selection of explanatory variables in regression or canonical redundancy analysis. The classical forward selection method presents two problems: a highly inflated Type I error and an overestimation of the amount of explained variance. Correcting these problems will greatly improve the performance of this very useful method in ecological modeling. To prevent the first problem, we propose a two-step procedure. First, a global test using all explanatory variables is carried out. If, and only if, the global test is significant, one can proceed with forward selection. To prevent overestimation of the explained variance, the forward selection has to be carried out with two stopping criteria: (1) the usual alpha significance level and (2) the adjusted coefficient of multiple determination (Ra(2)) calculated using all explanatory variables. When forward selection identifies a variable that brings one or the other criterion over the fixed threshold, that variable is rejected, and the procedure is stopped. This improved method is validated by simulations involving univariate and multivariate response data. An ecological example is presented using data from the Bryce Canyon National Park, Utah, U.S.A.
All-scale spatial analysis of ecological data by means of principal coordinates of neighbour matrices
DOI:10.1016/S0304-3800(01)00501-4 URL [本文引用: 1]
Dissecting the spatial structure of ecological data at multiple scales
DOI:10.1890/03-3111 URL [本文引用: 1]
Multispecies coexistence of trees in tropical forests:Spatial signals of topographic niche differentiation increase with environmental heterogeneity
Better environmental data may reverse conclusions about niche- and dispersal-based processes in community assembly
Variation partitioning of species composition into components explained by environmental and spatial variables is often used to identify a signature of niche- and dispersal-based processes in community assembly. Such interpretation, however, strongly depends on the quality of the environmental data available. In recent studies conducted in forest dynamics plots, the environment was represented only by readily available topographical variables. Using data from a subtropical broad-leaved dynamics plot in Taiwan, we focus on the question of how would the conclusion about importance of niche- and dispersal-based processes change if soil variables are also included in the analysis. To gain further insight, we introduced multiscale decomposition of a pure spatial component [c] in variation partitioning. Our results indicate that, if only topography is included, dispersal-based processes prevail, while including soil variables reverses this conclusion in favor of niche-based processes. Multiscale decomposition of [c] shows that if only topography was included, broad-scaled spatial variation prevails in [c], indicating that other as yet unmeasured environmental variables can be important. However, after also including soil variables this pattern disappears, increasing importance of meso- and fine-scaled spatial patterns indicative of dispersal processes.
Disentangling the importance of ecological niches from stochastic processes across scales
DOI:10.1098/rstb.2011.0063
URL
[本文引用: 1]
Deterministic theories in community ecology suggest that local, niche-based processes, such as environmental filtering, biotic interactions and interspecific trade-offs largely determine patterns of species diversity and composition. In contrast, more stochastic theories emphasize the importance of chance colonization, random extinction and ecological drift. The schisms between deterministic and stochastic perspectives, which date back to the earliest days of ecology, continue to fuel contemporary debates (e.g. niches versus neutrality). As illustrated by the pioneering studies of Robert H. MacArthur and co-workers, resolution to these debates requires consideration of how the importance of local processes changes across scales. Here, we develop a framework for disentangling the relative importance of deterministic and stochastic processes in generating site-to-site variation in species composition (β-diversity) along ecological gradients (disturbance, productivity and biotic interactions) and among biogeographic regions that differ in the size of the regional species pool. We illustrate how to discern the importance of deterministic processes using null-model approaches that explicitly account for local and regional factors that inherently create stochastic turnover. By embracing processes across scales, we can build a more synthetic framework for understanding how niches structure patterns of biodiversity in the face of stochastic processes that emerge from local and biogeographic factors.
A spatially explicit neutral model of beta-diversity in tropical forests
DOI:10.1006/tpbi.2002.1597
PMID:12167354
[本文引用: 1]
To represent species turnover in tropical rain forest, we use a neutral model where a tree's fate is not affected by what species it belongs to, seeds disperse a limited distance from their parents, and speciation is in equilibrium with random extinction. We calculate the similarity function, the probability F(r) that two trees separated by a distance r belong to the same species, assuming that the dispersal kernel P(r), the distribution of seeds about their parents and the prospects of mortality and reproduction, are the same for all trees regardless of their species. If P(r) is radially symmetric Gaussian with mean-square dispersal distance sigma, F(r) can be expressed in closed form. If P(r) is a radially symmetric Cauchy distribution, then, in two-dimensional space, F(r) is proportional to 1/r for large r. Analytical results are compared with individual-based simulations, and the relevance to field observations is discussed.
A review of beta diversity studies
DOI:10.3724/SP.J.1003.2010.323
[本文引用: 2]
<p>Beta diversity is an important component of biological diversity, measuring compositional change in species assemblages across temporal and spatial scales. Beta diversity concerns not only a number of ecological and evolutionary issues, but can also guide the selection of protected areas and help to optimize conservation networks. It has thus become a hot topic in biodiversity research in recent years. Researchers have used various measures and analytical methods to investigate patterns of beta diversity and its underlying mechanisms for various taxa and in different regions. Here, we reviewed literature from the past decade pertaining to the following aspects of beta diversity: metrics, temporal and spatial patterns, determinants and applications in biodiversity conservation. Whittaker introduced the term beta diversity in 1960, but defined it vaguely. As the concept of beta diversity evolved, a high variety of measures were developed to quantify the concept. The comparison of results from different studies may be hindered by the variety of measures used to quantify beta diversity. Presently, the most popular methods for measuring beta diversity are similarity/ dissimilarity coefficients such as Jaccard index and Sørensen index. In the last few years, several methods to quantify beta diversity have emerged, some of which are worth noting. Beta diversity depends on temporal scale, spatial scale and taxonomic scale, and decreases with increasing analytical grain size. There is no consensus among scientists that beta diversity decreases with latitude, i.e. that it is higher in tropics and lower near the poles. Beta diversity is high within mountain ranges and at the interface of biogeographic realms; thus, larger/more reserves are needed in these regions to cover the entire gradient of species turnover. Studies on beta diversity across temporal scales have shown that climatic change has resulted in shifts in species composition through time, and that the migration of species between different continents/regions has led to biotic homogenization. Based on a thorough review of beta diversity literature, we think the following questions might be the focus of future research: (1) the influence of evolutionary history and biological characteristics of different taxonomic groups on their beta diversity; (2) the influence of temporal/spatial scales on beta diversity and its determinants; and (3) the effect of anthropogenic activities on beta diversity.</p>
Beta多样性研究进展
DOI:10.3724/SP.J.1003.2010.323
[本文引用: 2]
Beta多样性度量时空尺度上物种组成的变化, 是生物多样性的重要组成部分, 与许多生态学和进化生物学问题密切相关, 并且其信息可用于保护区选址和布局规划, 因此在最近10年间成为生物多样性研究的热点问题之一。多年来, 学者们利用各种度量方式和分析方法, 在不同地理区域, 对许多生物类群beta多样性的时空格局和形成机制进行了大量研究。本文主要从beta多样性的度量方法、时空格局、形成机制及其在生物多样性保护中的应用等几个方面, 总结了最近10多年来相关研究的进展。Whittaker(1960)最初提出beta多样性概念时就缺乏严格的定义, 随着概念的不断演化, 度量方法也同样呈现出多样化, 而度量手段的多样化非常不利于不同研究之间的比较。目前应用最普遍的度量方法是采用相似性指数, 如Jaccard和Sørensen指数。最近几年, 新的度量方法还在不断出现, 其中一些方法非常值得注意。Beta多样性具有时空尺度和分类尺度依赖性, 一般随分析粒度(grain)的增加而降低。虽然有些研究表明beta多样性随纬度增加而降低, 但学者们并没有达成共识。山区和生物地理区的交界处beta多样性都比较高, 因而需要在这些地区增加保护区的面积或者数量以囊括物种变化梯度。对时间尺度上beta多样性的研究表明, 气候变化确实导致了物种组成在时间上的变化, 并且物种在不同大陆和地区间的迁移导致了生物同质化。扩散过程和生态位过程共同决定了beta多样性, 只是这两个过程的相对重要性依尺度、地理区域和物种类群的不同而有所差异。综上所述, 我们认为未来beta多样性研究的热点问题是:(1)不同生物类群的进化历史和生物学特征对beta多样性的影响; (2)不同的时空尺度对beta多样性及其维持机制的影响; (3)人类活动对beta多样性的影响。
Beta-diversity in tropical forest trees
DOI:10.1126/science.1066854
PMID:11809969
[本文引用: 1]
The high alpha-diversity of tropical forests has been amply documented, but beta-diversity-how species composition changes with distance-has seldom been studied. We present quantitative estimates of beta-diversity for tropical trees by comparing species composition of plots in lowland terra firme forest in Panama, Ecuador, and Peru. We compare observations with predictions derived from a neutral model in which habitat is uniform and only dispersal and speciation influence species turnover. We find that beta-diversity is higher in Panama than in western Amazonia and that patterns in both areas are inconsistent with the neutral model. In Panama, habitat variation appears to increase species turnover relative to Amazonia, where unexpectedly low turnover over great distances suggests that population densities of some species are bounded by as yet unidentified processes. At intermediate scales in both regions, observations can be matched by theory, suggesting that dispersal limitation, with speciation, influences species turnover.
The variation of tree beta diversity across a global network of forest plots
DOI:10.1111/j.1466-8238.2012.00770.x URL [本文引用: 4]
Above-ground biomass estimation in closed canopy neotropical forests using lidar remote sensing: Factors affecting the generality of relationships
Community ecology in the age of multivariate multiscale spatial analysis
DOI:10.1890/11-1183.1 URL [本文引用: 4]
Local and regional processes control species richness of plant communities: The species pool hypothesis
DOI:10.3724/SP.J.1003.2009.09141 URL [本文引用: 2]
局域和区域过程共同控制着群落的物种多样性: 种库假说
DOI:10.3724/SP.J.1003.2009.09141
[本文引用: 2]
解释群落的物种多样性大小是生态学研究的一个重要的理论和实践问题。人们提出了群落物种多样性的多种假说, Zobel等人提出的种库假说(species pool hypothesis)是生物多样性理论研究的重要发展。该假说认为, 一个群落的物种多样性不仅与环境条件和生态过程(ecological process)(如竞争、捕食)有关, 也受区域种库(regional species pool)的限制。区域种库是指一个地区可进入某一群落的潜在物种数量, 它由地史过程(如冰期、地质年代)和区域过程(物种形成、迁移扩散以及消亡)所决定。按照种库假说, 某一生境类型的面积越大, 地质年代越古老, 物种形成的机会也就越多, 因而能适应和分布于该生境的物种也就越多, 实际群落中的物种丰富度也就越高。种库在空间上主要有两个层次: 区域种库和实际种库, 前者指某一生境所拥有的潜在物种数量, 主要由生物地理过程(biogeographic processes)所决定; 后者则为调查的群落中实际出现的物种数量, 主要由竞争等生态过程和区域种库共同决定。本文对种库假说的基本概念、主要内容、种库确定方法等作了介绍, 并阐述了作者对这些问题的理解和认识。
Forest structure in space and time: Biotic and abiotic determinants of canopy complexity and their effects on net primary productivity
Changes in plant community diversity and floristic composition on environmental and geographical gradients
DOI:10.2307/2399464 URL [本文引用: 1]
Neutrality, niches, and dispersal in a temperate forest understory
Variation among European beetle taxa in patterns of distance decay of similarity suggests a major role of dispersal processes
DOI:10.1111/ecog.2018.v41.i11 URL [本文引用: 1]
Reconciling niche and neutrality: The continuum hypothesis
In this study, we ask if instead of being fundamentally opposed, niche and neutral theories could simply be located at the extremes of a continuum. First, we present a model of recruitment probabilities that combines both niche and neutral processes. From this model, we predict and test whether the relative importance of niche vs. neutral processes in controlling community dynamics will vary depending on community species richness, niche overlap and dispersal capabilities of species (both local and long distance). Results demonstrate that niche and neutrality form ends of a continuum from competitive to stochastic exclusion. In the absence of immigration, competitive exclusion tends to create a regular spacing of niches. However, immigration prevents the establishment of a limiting similarity. The equilibrium community consists of a set of complementary and redundant species, with their abundance determined, respectively, by the distribution of environmental conditions and the amount of immigration.
Advances for the new remote sensing technology in ecosystem ecology research
DOI:10.17521/cjpe.2019.0206 URL [本文引用: 1]
新一代遥感技术助力生态系统生态学研究
DOI:10.17521/cjpe.2019.0206
[本文引用: 1]
随着气候变化和人类活动的加剧, 生态系统正处于剧烈变化中, 生态学家需要从更大的时空尺度去理解生态系统过程和变化规律, 应对全球变化带来的威胁和挑战。传统地面调查方法主要获取的是样方尺度、离散的数据, 难以满足大尺度生态系统研究对数据时空连续性的要求。相比于传统地面调查方法, 遥感技术具有实时获取、重复监测以及多时空尺度的特点, 弥补了传统地面调查方法空间观测尺度有限的缺点。遥感通过分析电磁波信息从而识别地物属性和特征, 反演生态系统组成、能量流动和物质循环过程中的关键要素, 已逐渐成为生态学研究中必不可少的数据来源。近年来, 随着激光雷达、日光诱导叶绿素荧光等新型遥感技术以及无人机、背包等近地面遥感平台的发展, 个人化、定制化的近地面遥感观测逐渐成熟, 新一代遥感技术正在推动遥感信息“二维向三维”的转变, 为传统样地观测与卫星遥感之间搭建了尺度推绎桥梁, 这也给生态系统生态学带来了新的机遇, 推动生态系统生态学向多尺度、多过程、多学科、多途径发展。因此, 该文从生态系统生态学角度出发, 重点关注陆地生态系统中生物组分, 并分别从生态系统类型、结构、功能和生物多样性等方面, 结合作者在实际研究工作中的主要成果和该领域国际前沿动态, 阐述遥感技术在生态系统生态学中的研究现状并指出我国生态系统遥感监测领域发展方向及亟待解决的问题。
The role of canopy structural complexity in wood net primary production of a maturing northern deciduous forest
The even-aged northern hardwood forests of the Upper Great Lakes Region are undergoing an ecological transition during which structural and biotic complexity is increasing. Early-successional aspen (Populus spp.) and birch (Betula papyrifera) are senescing at an accelerating rate and are being replaced by middle-successional species including northern red oak (Quercus rubra), red maple (Acer rubrum), and white pine (Pinus strobus). Canopy structural complexity may increase due to forest age, canopy disturbances, and changing species diversity. More structurally complex canopies may enhance carbon (C) sequestration in old forests. We hypothesize that these biotic and structural alterations will result in increased structural complexity of the maturing canopy with implications for forest C uptake. At the University of Michigan Biological Station (UMBS), we combined a decade of observations of net primary productivity (NPP), leaf area index (LAI), site index, canopy tree-species diversity, and stand age with canopy structure measurements made with portable canopy lidar (PCL) in 30 forested plots. We then evaluated the relative impact of stand characteristics on productivity through succession using data collected over a nine-year period. We found that effects of canopy structural complexity on wood NPP (NPPw) were similar in magnitude to the effects of total leaf area and site quality. Furthermore, our results suggest that the effect of stand age on NPPw is mediated primarily through its effect on canopy structural complexity. Stand-level diversity of canopy-tree species was not significantly related to either canopy structure or NPPw. We conclude that increasing canopy structural complexity provides a mechanism for the potential maintenance of productivity in aging forests.
Exploring the relationships among canopy structure, stand productivity, and biodiversity of temperate forest ecosystems
Explaining variation in tropical plant community composition: Influence of environmental and spatial data quality
Generalizing hierarchical and variation partitioning in multiple regression and canonical analyses using the rdacca.hp R package
DOI:10.1111/mee3.v13.4 URL [本文引用: 2]
Assessing the scale-specific importance of niches and other spatial processes on beta diversity: A case study from a temperate forest
DOI:10.1007/s00442-008-1214-8
PMID:19018575
[本文引用: 1]
Niche processes and other spatial processes, such as dispersal, may simultaneously control beta diversity, yet their relative importance may shift across spatial and temporal scales. Although disentangling the relative importance of these processes has been a continuing methodological challenge, recent developments in multi-scale spatial and temporal modeling can now help ecologists estimate their scale-specific contributions. Here we present a statistical approach to (1) detect the presence of a space-time interaction on community composition and (2) estimate the scale-specific importance of environmental and spatial factors on beta diversity. To illustrate the applicability of this approach, we use a case study from a temperate forest understory where tree seedling abundances were monitored during a 9-year period at 40 permanent plots. We found no significant space-time interaction on tree seedling composition, which means that the spatial abundance patterns did not vary over the study period. However, for a given year the relative importance of niche processes and other spatial processes was found to be scale-specific. Tree seedling abundances were primarily controlled by a broad-scale environmental gradient, but within the confines of this gradient the finer scale patchiness was largely due to other spatial processes. This case study illustrates that these two sets of processes are not mutually exclusive and can affect abundance patterns in a scale-dependent manner. More importantly, the use of our methodology for future empirical studies should help in the merging of niche and neutral perspectives on beta diversity, an obvious next step for community ecology.
Lidar remote sensing for ecosystem studies
DOI:10.1641/0006-3568(2002)052[0019:LRSFES]2.0.CO;2 URL [本文引用: 1]
Analyzing beta diversity: Partitioning the spatial variation of community composition data
DOI:10.1890/05-0549 URL [本文引用: 3]
Partitioning beta diversity in a subtropical broad-leaved forest of China
DOI:10.1890/07-1880.1
PMID:19341137
[本文引用: 7]
The classical environmental control model assumes that species distribution is determined by the spatial variation of underlying habitat conditions. This niche-based model has recently been challenged by the neutral theory of biodiversity which assumes that ecological drift is a key process regulating species coexistence. Understanding the mechanisms that maintain biodiversity in communities critically depends on our ability to decompose the variation of diversity into the contributions of different processes affecting it. Here we investigated the effects of pure habitat, pure spatial, and spatially structured habitat processes on the distributions of species richness and species composition in a recently established 24-ha stem-mapping plot in the subtropical evergreen broad-leaved forest of Gutianshan National Nature Reserve in East China. We used the new spatial analysis method of principal coordinates of neighbor matrices (PCNM) to disentangle the contributions of these processes. The results showed that (1) habitat and space jointly explained approximately 53% of the variation in richness and approximately 65% of the variation in species composition, depending on the scale (sampling unit size); (2) tree diversity (richness and composition) in the Gutianshan forest was dominantly controlled by spatially structured habitat (24%) and habitat-independent spatial component (29%); the spatially independent habitat contributed a negligible effect (6%); (3) distributions of richness and species composition were strongly affected by altitude and terrain convexity, while the effects of slope and aspect were weak; (4) the spatial distribution of diversity in the forest was dominated by broad-scaled spatial variation; (5) environmental control on the one hand and unexplained spatial variation on the other (unmeasured environmental variables and neutral processes) corresponded to spatial structures with different scales in the Gutianshan forest plot; and (6) five habitat types were recognized; a few species were statistically significant indicators of three of these habitats, whereas two habitats had no significant indicator species. The results suggest that the diversity of the forest is equally governed by environmental control (30%) and neutral processes (29%). In the fine-scale analysis (10 x 10 m cells), neutral processes dominated (43%) over environmental control (20%).
The community-level consequences of seed dispersal patterns
DOI:10.1146/ecolsys.2003.34.issue-1 URL [本文引用: 1]
Forest structure drives changes in light heterogeneity during tropical secondary forest succession
DOI:10.1111/1365-2745.13680
PMID:34588706
[本文引用: 1]
Light is a key resource for tree performance and hence, tree species partition spatial and temporal gradients in light availability. Although light distribution drives tree performance and species replacement during secondary forest succession, we yet lack understanding how light distribution changes with tropical forest development.This study aims to evaluate how changes in forest structure lead to changes in vertical and horizontal light heterogeneity during tropical forest succession.We described successional patterns in light using a chronosequence approach in which we compared 14 Mexican secondary forest stands that differ in age (8-32 years) since agricultural abandonment. For each stand, we measured vertical light profiles in 16 grid cells, and structural parameters (diameter at breast height, height and crown dimensions) for each tree.During succession, we found a rapid increase in stand size (basal area, crown area and length) and stand differentiation (i.e. a gradual leaf distribution along the forest profile), which leads to fast changes in light conditions and more light heterogeneity. The inflection points of the vertical light gradient (i.e. the absolute height at which 50% relative light intensity is attained) rapidly moved towards higher heights in the first 20 years, indicating that larger amounts of light are intercepted by canopy trees. Light attenuation rate (i.e. the rate of light extinction) decreased during succession due to slower accumulation of the crown area with height. Understorey light intensity and heterogeneity slightly decreased during succession because of an increase in crown size and a decrease in lateral gap frequency. Understorey relative light intensity was 1.56% at 32 years after abandonment.. During succession, light conditions changed linearly, which should lead to a continuous and constant replacement of species. Especially in later successional stages, stronger vertical light gradients can limit the regeneration of light-demanding pioneer species and increase the proportion of shade-tolerant late-successional species under the canopy. These changes in light conditions were largely driven by the successional changes in forest structure, as basal area strongly determined the height where most light is absorbed, whereas crown area, and to a lesser extent crown length, determined light distribution.© 2021 The Authors. Journal of Ecology published by John Wiley & Sons Ltd on behalf of British Ecological Society.
Canopy height explains species richness in the largest clade of neotropical lianas
DOI:10.1111/geb.v29.1 URL [本文引用: 1]
Beta-diversity in temperate and tropical forests reflects dissimilar mechanisms of community assembly
DOI:10.1111/ele.12021
PMID:23113954
[本文引用: 2]
Site-to-site variation in species composition (β-diversity) generally increases from low- to high-diversity regions. Although biogeographical differences in community assembly mechanisms may explain this pattern, random sampling effects can create this pattern through differences in regional species pools. Here, we compared assembly mechanisms between spatially extensive networks of temperate and tropical forest plots with highly divergent species pools (46 vs. 607 species). After controlling for sampling effects, β-diversity of woody plants was similar and higher than expected by chance in both forests, reflecting strong intraspecific aggregation. However, different mechanisms appeared to explain aggregation in the two forests. In the temperate forest, aggregation reflected stronger environmental correlations, suggesting an important role for species-sorting (e.g. environmental filtering) processes, whereas in the tropics, aggregation reflected stronger spatial correlations, more likely reflecting dispersal limitation. We suggest that biogeographical differences in the relative importance of different community assembly mechanisms contribute to these striking gradients in global biodiversity.© 2012 Blackwell Publishing Ltd/CNRS.
Scale dependency in the functional form of the distance decay relationship
DOI:10.1111/ecog.2014.37.issue-4 URL [本文引用: 1]
Community assembly: The relative importance of neutral theory and niche theory
DOI:10.3724/SP.J.1003.2009.09142
[本文引用: 2]
Understanding species coexistence and the maintenance of biodiversity has long been the central interest of ecologists. The niche-based theory of community assembly has dominated community ecology for nearly a century, yet understanding of the mechanisms of species coexistence has remained elusive. The newly developed neutral theory of biodiversity has offered a promising alternative to the niche paradigm. The analytical elegance and simplicity of the neutral theory and its predictive power have made the theory widely popular. However, it is the very same simplicity of the theory (e.g. the symmetric assumption) that makes the theory vulnerable to stark criticisms. Widespread empirical evidence has shown that species in communities are not functionally symmetric; ecological equivalence is more a conceptual simplicity than a biological real-ism. Recognizing that niche and neutral processes do not have to diametrically oppose each other and a community is likely determined by the interplay of the two processes, ecologists currently are searching to reconcile the two theories by either incorporating drift into niche theory or niche into the neutral framework. However, this reconciliation process is still at its very early stage, we expect this direction will lead to a more complete understanding of community assembly mechanisms. In this paper, we provide a review on the brief histories of the niche and neutral theories, with the focus on comparing the distinct importance of the two theories in explaining community assembly. We discuss in details several integrated models that attempt to unify the niche and neutral theories. We argue that it is an essential step for any successful theory to with-stand substantial experimental and field tests. The experimental tests of neutral theories are an important di-rection that has currently not received due attention.
群落构建的中性理论和生态位理论
DOI:10.3724/SP.J.1003.2009.09142
[本文引用: 2]
物种共存和生物多样性维持一直是生态学研究的中心论题。基于物种生态位分化的群落构建理论已经发展了近一个世纪, 但我们对群落构建和生物多样性维持的机理仍然不清楚。近年来, 群落中性理论以其简约性和预测能力成为群落生态学研究的焦点, 但由于其“物种在生态功能上等价”的假设与大量研究结果相悖, 同时对自然群落结构的准确预测也只限于少数的生态系统, 因而饱受质疑。如今, 越来越多的生态学家认为群落构建的生态位理论与中性理论之争的最终归宿应该是二者的整合。 在本文中, 我们在简要回顾生态位理论和群落中性理论发展的基础上, 分析二者之间的主要分歧和互补性, 试图梳理二者整合的途径。我们认为, 尽管中性理论的发展极大地丰富了群落构建理论, 但二者的整合尚处于初级阶段; 群落构建零模型假说、中性—生态位连续体假说、随机生态位假说等都不失为有价值的尝试, 今后需要在其他类型的生态系统中进行实验验证, 以更好地理解确定性过程和随机过程在决定群落构建和生物多样性维持中的作用。
A latitudinal gradient in large-scale beta diversity for vascular plants in North America
DOI:10.1111/j.1461-0248.2007.01066.x
PMID:17594429
[本文引用: 2]
Species turnover, or beta diversity, has been predicted to decrease with increasing latitude, but few studies have tested this relationship. Here, we examined the beta diversity-latitude relationship for vascular plants at a continental scale, based on complete species lists of native vascular plants for entire states or provinces in North America (north of Mexico). We calculated beta diversity as the slope of the relationship between the natural logarithm of the Jaccard index (lnJ ) for families, genera or species, and both geographic distance and climate difference within five latitude zones. We found that beta diversity decreased from south to north; within latitude zones, it decreased from species to genera and families. Geographic and climatic distance explained about the same proportion of the variance in lnJ in zones south of c. 50 degrees N. North of this latitude, nearly all the explained variance in lnJ was attributable to geographic distance. Therefore, decreasing beta diversity from south to north reflects decreasing climate differentiation within more northerly latitude zones, and primarily post-glacial dispersal limitation north of 50 degrees N.
R: A Language and Environment for Statistical Computing
Community diversity: Relative roles of local and regional processes
The species richness (diversity) of local plant and animal assemblages-biological communities-balances regional processes of species formation and geographic dispersal, which add species to communities, against processes of predation, competitive exclusion, adaptation, and stochastic variation, which may promote local extinction. During the past three decades, ecologists have sought to explain differences in local diversity by the influence of the physical environment on local interactions among species, interactions that are generally believed to limit the number of coexisting species. But diversity of the biological community often fails to converge under similar physical conditions, and local diversity bears a demonstrable dependence upon regional diversity. These observations suggest that regional and historical processes, as well as unique events and circumstances, profoundly influence local community structure. Ecologists must broaden their concepts of community processes and incorporate data from systematics, biogeography, and paleontology into analyses of ecological patterns and tests of community theory.
When can we distinguish between neutral and non-neutral processes in community dynamics under ecological drift?
DOI:10.1111/j.1461-0248.2009.01346.x
PMID:19570103
[本文引用: 1]
Determining whether the composition of ecological communities (species presence and abundance), can be predicted from species demographic traits, rather than being a result of neutral drift, is a key ecological question. Here we compare the similarity of community composition, from different community assembly models run under identical environmental conditions, where interspecific competition is assumed to be either neutral or niche-based. In both cases, species colonize a focal patch from a network of neighbouring patches in a metacommunity. We highlight the circumstances (rate and spatial scale of dispersal, and the relative importance of ecological drift) where commonly used community similarity metrics or species rank-abundance relationships are likely to give similar results, regardless of the underlying processes (neutral or non-neural) driving species' dynamics. As drift becomes more important in driving species abundances, deterministic niche structure has a smaller influence. Our ability to discriminate between different underlying processes driving community organization depends on the relative importance of different drift processes that operate on different spatial scales.
Seed dispersal and spatial pattern in tropical trees
DOI:10.1371/journal.pbio.0040344
PMID:17048988
[本文引用: 1]
Theories of tropical tree diversity emphasize dispersal limitation as a potential mechanism for separating species in space and reducing competitive exclusion. We compared the dispersal morphologies, fruit sizes, and spatial distributions of 561 tree species within a fully mapped, 50-hectare plot of primary tropical forest in peninsular Malaysia. We demonstrate here that the extent and scale of conspecific spatial aggregation is correlated with the mode of seed dispersal. This relationship holds for saplings as well as for mature trees. Phylogenetically independent contrasts confirm that the relationship between dispersal and spatial pattern is significant even after controlling for common ancestry among species. We found the same qualitative results for a 50-hectare tropical forest plot in Panama. Our results provide broad empirical evidence for the importance of dispersal mode in establishing the long-term community structure of tropical forests.
Variation partitioning as a tool to distinguish between niche and neutral processes
DOI:10.1111/eco.2010.33.issue-4 URL [本文引用: 1]
The distance decay of similarity in ecological communities
DOI:10.1111/eco.2007.30.issue-1 URL [本文引用: 1]
Current measures for distance decay in similarity of species composition are influenced by study extent and grain size
DOI:10.1111/j.1466-8238.2012.00772.x URL [本文引用: 1]
Forest structure and tree species distribution in relation to topography-mediated heterogeneity of soil nitrogen and light at the forest floor
DOI:10.1046/j.1440-1703.2003.00578.x URL [本文引用: 1]
Forest structure, not climate, is the primary driver of functional diversity in northeastern North America
DOI:10.1016/j.scitotenv.2020.143070 URL [本文引用: 1]
Patterns and determinants of floristic variation across lowland forests of Bolivia
DOI:10.1111/btp.2011.43.issue-4 URL [本文引用: 1]
Dispersal, environment, and floristic variation of western Amazonian forests
DOI:10.1126/science.1078037
PMID:12522248
[本文引用: 1]
The distribution of plant species, the species compositions of different sites, and the factors that affect them in tropical rain forests are not well understood. The main hypotheses are that species composition is either (i) uniform over large areas, (ii) random but spatially autocorrelated because of dispersal limitation, or (iii) patchy and environmentally determined. Here we test these hypotheses, using a large data set from western Amazonia. The uniformity hypothesis gains no support, but the other hypotheses do. Environmental determinism explains a larger proportion of the variation in floristic differences between sites than does dispersal limitation; together, these processes explain 70 to 75% of the variation. Consequently, it is important that management planning for conservation and resource use take into account both habitat heterogeneity and biogeographic differences.
Conceptual synthesis in community ecology
DOI:10.1086/652373 URL [本文引用: 1]
Species composition and community structure of a 20 hm2 plot of mid-mountain moist evergreen broad-leaved forest on the Mts. Ailaoshan, Yunnan Province, China
DOI:10.17521/cjpe.2017.0272 URL [本文引用: 3]
云南哀牢山中山湿性常绿阔叶林20 hm2动态样地的物种组成与群落结构
DOI:10.17521/cjpe.2017.0272
[本文引用: 3]
中山湿性常绿阔叶林是分布在我国亚热带气候区的一种山地森林植被。为监测此类森林的动态过程, 按照Centre for Tropical Forest Science的建设标准, 于2014年在云南省景东县徐家坝附近的中山湿性常绿阔叶林中建立了一块20 hm <sup>2</sup>的森林动态样地, 测量并记录了样地中所有胸径(DBH) ≥ 1 cm的树木直径及其分枝的直径, 并对其挂牌标记、定位和鉴定, 分析了其物种组成和群落结构。结果显示: 样地内共有DBH ≥ 1 cm的木本植物独立个体44 168株, 隶属于36科63属104种。重要值最大的前3个科依次是壳斗科、茶科和樟科。在属的水平上, 热带区系成分占总属数的46.0%, 温带区系成分占38.1%。重要值≥1的物种有22个, 占总个体数的84.6%。重要值最大的3个种依次是蒙自连蕊茶(Camellia forrestii)、云南越桔(Vaccinium duclouxii)和多花山矾(Symplocos ramosissima)。胸高断面积之和排名前4名的物种为硬斗柯(Lithocarpus hancei)、木果柯(L. xylocarpus)、变色锥(Castanopsis wattii)和南洋木荷(Schima noronhae), 它们同时也是该群落林冠层的优势树种。样地内所有个体的径级分布呈倒“J”型, 群落有充足的增补个体, 如蒙自连蕊茶和多花山矾等。稀有种(个体数少于20的物种)共计49种, 占总物种数的47.1%。常绿木本植物在样地内分别占总重要值、总多度和总胸高断面积的94.7%、96.2%和94.0%, 优势明显。
Vegetation of the Great Smoky Mountains
DOI:10.2307/1943577 URL [本文引用: 1]
Driving forces underlying the beta diversity of tree species in subtropical mid-mountain moist evergreen broad-leaved forests in Ailao Mountains
DOI:10.17520/biods.2019356
[本文引用: 1]
Beta diversity refers to species composition variation among communities across temporal and spatial scales. Beta diversity includes species turnover and species richness differences between communities. The ecological processes that drive beta diversity patterns are determined by spatio-temporal dynamics of communities. However, the driving forces that form beta diversity and its components patterns are still controversial. Previous studies have shown that beta diversity patterns are scale-dependent as are the relative importance of underlying ecological processes. In this study, the beta diversity of tree species in the 20 ha subtropical mid-mountain moist evergreen broad-leaved forest dynamics plot in Ailao Mountains was studied. Across different spatial scales, the Bray-Curtis indices among quadrat pairs were partitioned into species turnover components and species richness components. The relative importance of scale dependent environmental filtering and dispersal limitation on beta diversity were analyzed by using a redundancy analysis and variation partitioning analysis. Our results showed that: (1) Beta diversity and its components decreased with increasing scale. The pairwise difference in species composition between quadrats was dominated by species turnover components at all scales. (2) With increasing scale, the relative importance of environment filtering on beta diversity gradually increased, while the relative importance of dispersal limitation gradually decreased. This study confirmed the importance of spatial scale on beta diversity pattern and the quantitative assessment of its driving forces. Future research should focus more on examining the mechanism of the scale effects on beta diversity and its underlying driving forces.
哀牢山亚热带中山湿性常绿阔叶林树种beta多样性格局形成的驱动力
DOI:10.17520/biods.2019356
[本文引用: 1]
Beta多样性通常指群落在时间和空间上物种组成的差异, 包括物种周转组分和物种丰富度差异组分。驱动beta多样性格局形成的生态过程决定了群落的时空动态, 然而关于beta多样性及其两个组分格局形成的驱动力还存在较多争议。以往研究表明, beta多样性的格局存在取样尺度的依赖性, 驱动其形成的生态过程在不同取样尺度下的相对重要性也随之改变。本研究以哀牢山亚热带中山湿性常绿阔叶林20 ha动态监测样地为研究对象, 在不同取样尺度上, 将样方间的Bray-Curtis指数分解为物种周转组分和物种丰富度差异组分, 通过典范冗余分析和方差分解的方法揭示环境过滤和扩散限制对于beta多样性及其两个组分格局形成的相对重要性及其尺度依赖性。结果表明: (1) beta多样性、物种周转组分和物种丰富度差异组分均随取样尺度的增大而减小。在不同取样尺度下, 物种周转组分对于beta多样性的贡献始终占主导地位。(2)随着取样尺度的增大, 环境过滤驱动beta多样性格局形成的相对重要性逐渐增加, 而扩散限制的相对重要性逐渐降低。本研究进一步证实了取样尺度在beta多样性格局形成及其驱动力定量评价中的重要性, 今后的研究需要进一步解析上述尺度效应的形成机制。
From canopy complementarity to asymmetric competition: The negative relationship between structural diversity and productivity during succession
DOI:10.1111/jec.v110.2 URL [本文引用: 1]
Multi-scale comparison of topographic complexity indices in relation to plant species richness
DOI:10.1016/j.ecocom.2015.02.007 URL [本文引用: 3]
Half-century evidence from western Canada shows forest dynamics are primarily driven by competition followed by climate
Drone-acquired data reveal the importance of forest canopy structure in predicting tree diversity
DOI:10.1016/j.foreco.2021.119945 URL [本文引用: 3]
Canopy structure is an important factor driving local-scale woody plant functional beta diversity
DOI:10.17520/biods.2020092
[本文引用: 2]
Functional beta diversity refers to the variation of functional composition between communities. Exploring the mechanisms underlying functional beta diversity is a central theme in community ecology. We measured 11 important functional traits of woody plants in 20 ha forest dynamics plot in Xishuangbanna tropical seasonal rainforest and used abundance-weighted mean nearest neighbor trait distance to quantify the functional beta diversity at different sampling scales. We revealed the relative importance of canopy structure, environmental heterogeneity, and spatial distance on functional beta diversity using multiple regressions on distance matrices. Our results showed that, for all woody plant individuals with DBH ≥ 1 cm, the best model to explain the functional beta diversity was one including canopy structure, environment, and spatial distance. At each of the three sampling scales, canopy structure and environment had relatively large explanatory power and increased with increasing sampling scale, while the relative importance of spatial distance was negligible. Our findings corroborate that environmental heterogeneity and spatial distance are the two main factors driving functional beta diversity, and we provide new mechanistic insights by including the effects of canopy cover at local scales.
林冠结构是局域尺度木本植物功能性状beta多样性形成的重要驱动力
DOI:10.17520/biods.2020092
[本文引用: 2]
功能性状beta多样性反映了群落间功能性状组成的差异, 解析其形成机制是群落生态学研究的核心内容之一。本研究以云南西双版纳热带季节雨林20 ha动态监测样地为研究对象, 测定木本植物11个重要的功能性状, 采用多度加权的平均最近邻体性状距离度量不同取样尺度的功能性状beta多样性, 基于距离矩阵的多元回归方法解析林冠结构差异、环境异质性、空间距离在功能性状beta多样性格局形成中的相对作用。结果表明, 对于所有木本植物个体(DBH ≥ 1 cm)而言, 同时考虑林冠结构、环境和空间距离的模型为解释功能性状beta多样性格局的最优模型; 在3个不同取样尺度上, 林冠结构差异和环境距离都对功能性状beta多样性具有较大的解释力, 且随着取样尺度的增大而上升, 空间距离的作用基本可以忽略。本研究证实了林冠结构是局域尺度木本植物功能性状beta多样性格局形成的重要驱动力, 这一发现更新了环境异质性和空间距离是驱动功能性状beta多样性格局形成的主要因素的传统认知, 为将来研究功能性状beta多样性形成机制提供新的视角, 并证实了取样尺度在解析木本植物功能性状beta多样性格局形成机制中的重要性。
Vegetation geography of evergreen broad-leaved forests in Yunnan, southwestern China
DOI:10.17521/cjpe.2020.0302 URL [本文引用: 1]
云南常绿阔叶林的植被地理研究
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