首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 62 毫秒
1.
生物多样性是生态系统复杂性的重要特征, 理解多样性的形成和维持机制一直是理论生态学研究的核心议题。本文从三方面概述了生物多样性理论的最新进展。一是物种共存和群落构建, 总结了现代共存理论和基于过程的群落构建理论的新进展。二是物种相互作用, 综述了利用经验数据推断物种相互作用关系和强度的最新方法。三是生态-进化动态, 介绍了生态-进化模型的一般框架及其在生物多样性研究中的应用。最后对生物多样性理论的发展趋势做了展望, 特别是多尺度整合理论和全球变化下的预测理论。  相似文献   

2.
群落生态学的中性理论   总被引:15,自引:0,他引:15       下载免费PDF全文
 生物多样性的分布格局和维持机制一直是群落生态学研究的核心问题,其中的关键是物种的共存机制。长 期以来,生态位分化的思想在这一研究领域占据着主导地位。然而这一理论在解释热带雨林很高的物种多 样性时遇到了困难。而以Hubbell为代表提出的群落中性漂变理论则假定在同一营养级物种构成的群落中 不同物种的不同个体在生态学上可看成是完全等同的;物种的多度随机游走,群落中的物种数取决于物种 灭绝和物种迁入/新物种形成之间的动态平衡。在这一假定之下,该理论预言了两种统计分布。一种是集 合群落在点突变形成新物种的模式下其各个物种相对多度服从对数级数分布,而受扩散限制的局域群落以 及按照随机分裂为新物种模式形成的集合群落则服从零和多项式分布。与生态位理论相反,中性理论不以 种间生态位差异作为研究群落结构的出发点,而是以物种间在个体水平上的对等性作为前提。该理论第一 次从基本生态学过程(出生、死亡、迁移、物种分化)出发,给出了群落物种多度分布的机理性解释,同 时其预测的物种多度分布格局在实际群落中也得到了广泛的印证。因此,中性理论自诞生以来便在生态学 界引发了极大的反响,也包括一些反对的声音。该文重点综述了关于中性理论的假设、预测和物种形成模 式等方面的最新研究进展,包括中性理论本身的发展、关于中性理论的假设和预测的合理性检验以及在集 合群落尺度上物种分化模式的讨论;并指出未来发展方向可能是在生态位理论和中性理论之间架起一座桥 梁,同时发展包含随机性的群落生态位模型,以及允许种间差异的近中性模型。  相似文献   

3.
种、种的多样性及退化生态系统功能的恢复和维持研究   总被引:41,自引:8,他引:33  
物种多样性是生态系统的重要特征并维持系统的功能支行,生物种和不同种类构成的群落为人类提供诸如营养物质循环、生物生产力、营养功能等形式的重要生态服务,特种多样性与生态系统抵御逆境和干扰的能力紧密相关,多样性的提高会增加系统的稳定性,与单个种和种类的数量相比,功能群和功能多样性对生态系统功能的影响效应要大得多,且易于被用来测度稳定性和预测群落变化,本文提出并探讨了种对生态系统功能作用的几种形式,理解物种多样性与生态系统的功能关系能指导退化生态系统恢复和维持其功能的实践活动,尤其为恢复的初始阶段进行群落的“种类组装”提供生态理论基础。  相似文献   

4.
提出生物多样性分布格局的普适性理论和探索其内在形成机制一直是生态学家们研究的焦点之一.到目前为止,已有很多假说被用来解释生物多样性分布规律,但是这些假说的普适性均受到学者们的质疑.最新理论--代谢速率假说以能量相当法则和代谢分形分配网络模型为基础,定量预测了个体及种群生态进化动态过程与群落生物多样性分布格局之间的关系,以及物种丰富度和环境因子之间的关系.代谢速率假说解释了生物多样性的起源问题,也回答了生物多样性如何维持的问题.该文重点综述了代谢生物多样性理论的发展及其相关研究进展.通过和其他假说比较、分析,我们认为随着代谢理论假说的不断发展和完善,代谢生物多样性理论将更具有普适性.同时我们也提出了进一步完善该假说需要解决的一些科学问题.  相似文献   

5.
应用中性理论分析局域群落中的物种多样性及稳定性   总被引:7,自引:2,他引:5  
张立敏  陈斌  李正跃 《生态学报》2010,30(6):1556-1563
如何解释群落中物种的丰富与稀少,并对物种多样性和群落稳定性进行合理的量化评价是群落生态学研究中的一个热点问题。20世纪中期,MacArthur将影响自然群落稳定性的因素归结为物种数量多少以及物种间相互作用的大小,20世纪末Doak等学者提出群落的容纳能力和物种间的维持机制是决定群落稳定性的关键因素。同时对群落结构及物种间维持机制的研究也有了新的突破,Hubbell提出"生物多样性与生物地理学统一的中性理论(Unified Neutral Theory of Biodiversity and Biogeography)"为群落生态学研究提供了新的思路和方法。从群落中性理论的基本假设出发,对Hubbell中性理论中局域群落的物种多度动态模型进行分析,归纳得出群落中性理论中物种多样性与群落稳定性之间的量化关系。封闭的局域群落中,出现物种灭绝或单物种独占的时间与群落大小及物种相对多度成正比,物种多样性程度的增加可延长物种灭绝或独占的时间;开放的局域群落中,物种多度期望值与局域群落大小、物种在集合群落中的物种相对多度成正比,周围群落中物种的灭绝会引起局域群落中相应物种的灭绝,最终导致整个生态群落物种多样性的降低;群落中物种多度的方差与局域群落大小、迁移率、物种在集合群落中的物种相对多度相关,局域群落物种多度的波动幅度随着群落间生态隔离的减弱或物种多样性程度的增加而减小。由此,集合群落物种多样性是影响局域群落物种多样性的重要因素,生态隔离程度的减弱及物种多样性的增加都将增强群落的稳定性。  相似文献   

6.
植物群落构建机制研究进展   总被引:25,自引:15,他引:10  
柴永福  岳明 《生态学报》2016,36(15):4557-4572
群落构建研究对于解释物种共存和物种多样性的维持是至关重要的,因此一直是生态学研究的中心论题。尽管近年来关于生态位和中性理论的验证研究已经取得了显著的成果,但对于局域群落构建机制的认识仍存在很大争议。随着统计和理论上的进步使得用功能性状和群落谱系结构解释群落构建机制变为可能,主要是通过验证共存物种的性状和谱系距离分布模式来实现。然而,谱系和功能性状不能相互替代,多种生物和非生物因子同时控制着群落构建,基于中性理论的扩散限制、基于生态位的环境过滤和竞争排斥等多个过程可能同时影响着群落的构建。所以,综合考虑多种方法和影响因素探讨植物群落的构建机制,对于预测和解释植被对干扰的响应,理解生物多样性维持机制有重要意义。试图在简要回顾群落构建理论及研究方法发展的基础上,梳理其最新研究进展,并探讨整合功能性状及群落谱系结构的研究方法,解释群落构建和物种多样性维持机制的可能途径。在结合功能性状和谱系结构研究群落构建时,除了考虑空间尺度、环境因子、植被类型外,还应该关注时间尺度、选择性状的种类和数量、性状的种内变异、以及人为干扰等因素对群落构建的影响。  相似文献   

7.
理解群落构建过程可以解释生物多样性格局的形成和维持,对于生物多样性保护起到关键作用。生态位理论是群落构建研究的核心框架之一。该理论认为群落构建是生物作用和非生物作用将区域物种库中的物种选入局域群落的确定过程。近年来,随着该领域受到的关注越来越多,研究者不但从物种、谱系或功能等生物多样性维度来研究群落构建,所使用的多样性指数、零模型算法和物种库界定方式等也多种多样。本文回顾了从生物多样性不同维度研究群落构建的优势与局限,总结了群落构建过程中构建零模型和界定物种库时需要注意的一些问题,介绍了部分群落构建研究的最新方法学进展和研究成果。最后,结合近年来的研究案例提出了对未来群落构建研究的一些建议。  相似文献   

8.
贾鹏  杜国祯 《生命科学》2014,(2):153-157
生物多样性是生态学的核心问题。传统的多样性指数仅包含物种数和相对多度的信息,这类基于分类学的多样性指数并不能很好地帮助理解群落构建和生态系统功能。不同物种对群落构建和生态系统功能所起到的作用类型和贡献也不完全相同,且物种在生态过程中的作用和贡献往往与性状密切相关,因此功能多样性已经成为反映物种群落构建、干扰以及环境因素对群落影响的重要指标。同时,由于亲缘关系相近的物种往往具有相似的性状,系统发育多样性也可以作为功能多样性的一个替代。功能多样性和系统发育多样性各自具有优缺点,但二者均比分类多样性更能揭示群落和生态系统的构建、维持与功能。  相似文献   

9.
局域和区域过程共同控制着群落的物种多样性:种库假说   总被引:7,自引:2,他引:5  
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。  相似文献   

10.
群落内的多物种如何共存是群落生态学的核心研究内容之一。经典的物种共存理论强调物种之间的生态位分化,注重具体共存机制的研究。这种以具体共存机制为研究对象的方法一定程度上促进了当代物种共存理论框架的形成。在当代物种共存理论框架下,物种间的差异被划分为两类综合性的抽象差异——生态位差异和平均适合度差异,前者促进物种共存,对应稳定化机制;后者导致竞争排除,对应均等化机制。本文在简要回顾经典物种共存理论的基础上,介绍了当代物种共存理论的框架(包括理论的形成和定义)、基于该理论的部分实验验证工作及其在一些重要生态学问题中的应用。当代物种共存理论不仅揭示了群落内物种是如何共存的这一基本理论问题,更重要的是在全球变化的背景下该理论对生物多样性的保护和管理具有重要的应用价值。期望本文的介绍有助于国内生态学和生物多样性工作者了解当代物种共存理论,并将其应用于群落构建和生物多样性维持机制等方面的研究。  相似文献   

11.
Aim  The invasion of natural communities by alien species represents a serious threat, but creates opportunities to learn about community functions. Neutral theory proposes that the niche concept may not be needed to explain the assemblage and diversity of natural communities, challenging the classical view of community ecology and generating a lasting debate. Biological invasions, when considered as natural experiments, can be used to contrast some of the predictions of neutral and classic niche theories.
Location  Global.
Methods  We use data from biological invasions as natural experiments to contrast some of the fundamental predictions of neutral theory.
Results  Some emerging patterns did not differ from neutral model expectations (e.g. the relationship between native and exotic species richness, invasibility of resource-rich habitats, and the relationship between propagule release and invasion success). Nevertheless, other patterns (e.g. experimental evidence of the relationship between diversity and susceptibility to invasion, the invasion of communities with a low resource availability, invasiveness related to species traits) contrasted with the predictions that can be inferred from neutral theory.
Main conclusions  Neutral theory correctly highlights the need to include randomness in models of community structure. Biological invasion patterns show that neutral forces are important in structuring natural communities, but the patterns differ from those inferred from a complete neutral model. For biodiversity-conservation purposes, the implications of accepting or not accepting neutral theory as a process-based theory are very important.  相似文献   

12.
13.
A new analysis of the nearly century‐old Lotka–Volterra theory allows us to link species interactions to biodiversity patterns, including: species abundance distributions, estimates of total community size, patterns of community invasibility, and predicted responses to disturbance. Based on a few restrictive assumptions about species interactions, our calculations require only that the community is sufficiently large to allow a mean‐field approximation. We develop this analysis to show how an initial assemblage of species with varying interaction strengths is predicted to sort out into the final community based on the species’ predicted target densities. The sorting process yields predictions of covarying patterns of species abundance, community size, and species interaction strengths. These predictions can be tested using enrichment experiments, examination of latitudinal and productivity gradients, and features of community assembly.  相似文献   

14.
Theoretical predictions for biodiversity patterns are typically derived under the assumption that ecological systems have reached a dynamic equilibrium. Yet, there is increasing evidence that various aspects of ecological systems, including (but not limited to) species richness, are not at equilibrium. Here, we use simulations to analyse how biodiversity patterns unfold through time. In particular, we focus on the relative time required for various biodiversity patterns (macroecological or phylogenetic) to reach equilibrium. We simulate spatially explicit metacommunities according to the Neutral Theory of Biodiversity (NTB) under three modes of speciation, which differ in how evenly a parent species is split between its two daughter species. We find that species richness stabilizes first, followed by species area relationships (SAR) and finally species abundance distributions (SAD). The difference in timing of equilibrium between these different macroecological patterns is the largest when the split of individuals between sibling species at speciation is the most uneven. Phylogenetic patterns of biodiversity take even longer to stabilize (tens to hundreds of times longer than species richness) so that equilibrium predictions from neutral theory for these patterns are unlikely to be relevant. Our results suggest that it may be unwise to assume that biodiversity patterns are at equilibrium and provide a first step in studying how these patterns unfold through time.  相似文献   

15.
The neutral theory of biodiversity purports that patterns in the distribution and abundance of species do not depend on adaptive differences between species (i.e. niche differentiation) but solely on random fluctuations in population size (“ecological drift”), along with dispersal and speciation. In this framework, the ultimate driver of biodiversity is speciation. However, the original neutral theory made strongly simplifying assumptions about the mechanisms of speciation, which has led to some clearly unrealistic predictions. In response, several recent studies have combined neutral community models with more elaborate speciation models. These efforts have alleviated some of the problems of the earlier approaches, while confirming the general ability of neutral theory to predict empirical patterns of biodiversity. However, the models also show that the mode of speciation can have a strong impact on relative species abundances. Future work should compare these results to diversity patterns arising from non‐neutral modes of speciation, such as adaptive radiations.  相似文献   

16.
琅琊山国家森林公园蝶类多样性   总被引:5,自引:0,他引:5  
诸立新  吴孝兵 《昆虫知识》2006,43(2):232-235,225
报道了安徽滁州市琅琊山国家森林公园蝶类多样性的研究结果,共采集了蝴蝶4454只,隶属8科、40属、57种。应用Margalef物种丰富度模型及Shannon-Wiener生物多样性指数分析了该地蝶类物种的丰富度及多样性。蝴蝶物种丰富度由大到小为森林林地(7.2747)>山缘农田(5.3499)>裸岩(3.3008),物种多样性指数由大到小为森林林地(3.3081)>裸岩(2.4628)>山缘农田(2.0009);结果表明琅琊山蝶类物种较为丰富,多样性指数说明琅琊山的生态环境良好。  相似文献   

17.
Quantifying diversity is of central importance for the study of structure, function and evolution of microbial communities. The estimation of microbial diversity has received renewed attention with the advent of large-scale metagenomic studies. Here, we consider what the diversity observed in a sample tells us about the diversity of the community being sampled. First, we argue that one cannot reliably estimate the absolute and relative number of microbial species present in a community without making unsupported assumptions about species abundance distributions. The reason for this is that sample data do not contain information about the number of rare species in the tail of species abundance distributions. We illustrate the difficulty in comparing species richness estimates by applying Chao''s estimator of species richness to a set of in silico communities: they are ranked incorrectly in the presence of large numbers of rare species. Next, we extend our analysis to a general family of diversity metrics (‘Hill diversities''), and construct lower and upper estimates of diversity values consistent with the sample data. The theory generalizes Chao''s estimator, which we retrieve as the lower estimate of species richness. We show that Shannon and Simpson diversity can be robustly estimated for the in silico communities. We analyze nine metagenomic data sets from a wide range of environments, and show that our findings are relevant for empirically-sampled communities. Hence, we recommend the use of Shannon and Simpson diversity rather than species richness in efforts to quantify and compare microbial diversity.  相似文献   

18.
19.
Published in 2001, The Unified Neutral Theory of Biodiversity and Biogeography (UNTB) emphasizes the importance of stochastic processes in ecological community structure, and has challenged the traditional niche‐based view of ecology. While neutral models have since been applied to a broad range of ecological and macroecological phenomena, the majority of research relating to neutral theory has focused exclusively on the species abundance distribution (SAD). Here, we synthesize the large body of work on neutral theory in the context of the species abundance distribution, with a particular focus on integrating ideas from neutral theory with traditional niche theory. First, we summarize the basic tenets of neutral theory; both in general and in the context of SADs. Second, we explore the issues associated with neutral theory and the SAD, such as complications with fitting and model comparison, the underlying assumptions of neutral models, and the difficultly of linking pattern to process. Third, we highlight the advances in understanding of SADs that have resulted from neutral theory and models. Finally, we focus consideration on recent developments aimed at unifying neutral‐ and niche‐based approaches to ecology, with a particular emphasis on what this means for SAD theory, embracing, for instance, ideas of emergent neutrality and stochastic niche theory. We put forward the argument that the prospect of the unification of niche and neutral perspectives represents one of the most promising future avenues of neutral theory research.  相似文献   

20.
选用描述种-多度关系的二类共8个模型(对数级数分布LS、对数正态分布LN、负二项分布NB和几何分布GOM以及“分割线段”模型BSM、生态位优先占领模型NPM、Zipf模型ZM和Zipf-Mandelbrot模型ZMM)对东灵山地区9个类型的森林群落进行了研究。结果表明,LS和NB对大多数群落可以很好地拟合,LN和GOM对每一个群落都不能很好地拟合;ZMM可以很好地、NPM也可以较好地拟合每一个群落,ZM可以很好地拟合大多数群落,而BSM则反之。LS中的参数α与4个丰富度指数呈极强的线性关系,与3个多样性指数也有较强的线性关系。因此,α可以作为群落的一个多样性指数使用,并且它更多地反映了群落的丰富度。本研究也表明,将包含多个参数的非线性方程组逐渐化为只含一个参数的非线性方程,再将MonteCarlo方法、区间二分法和迭代法相结合以求解该方程,从而实现参数估计,这种算法是可行的;在拟合三参数模型ZMM时,先固定参数β,再通过线性化求出另外2个参数,经过多次计算,求出一组参数值作为下一步非线性方程拟合的初值,这种算法也是成功的。在进行种重要性顺序-多度表模型的评价时,不能只考虑剩余标准差或相关指数,它们是基于误差平方和的两个指标,对真实的误差有某种夸张作用;应该尽可能地考虑平均绝对误差这个指标。  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号