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1.
生境变化对集合种群系统生态效应的影响   总被引:26,自引:15,他引:11  
林振山 《生态学报》2003,23(3):480-485
通过大量的数值模拟发现 :生境恢复或扩展将导致集合种群的强弱序由自然数的顺序规律演变为奇数种群强 -偶数种群弱 ,同时集合种群里的最优秀种群将迅速扩张、发展为更为强大的最优势种。而当生境遭受到破坏 (毁坏 ) ,集合种群里的最优秀种群将迅速地伦为最弱者。如果栖息地的毁坏率大于集合种群优势种对栖息地的占有率 ,不仅集合种群里的优势种群将不可避免地灭绝 ,伴随最优秀种群走向灭绝的种群依次还有第二、第三、第四强等的种群。同时 ,将导致集合种群的强弱序由自然数的顺序规律演变为偶数种群强 -奇数种群弱。  相似文献   

2.
生境变化对集合种群系统生态效的影响   总被引:2,自引:0,他引:2  
林振山 《生态学报》2003,23(3):480-485
通过大量的数值模拟发现:生境恢复或扩展将导致集合种群的强弱序由自然数的顺序规律演变为奇数种群强-偶数种群弱,同时集合种群里的最优秀种群将迅速扩张,发展为更为强大的最优势种,而当生境遭受到破坏(毁坏),集合种群里的最优秀种群将迅速地伦为最弱者,如果栖息地的毁坏率大于集合种群优势种对栖息地的占有率,不仅集合种群里的优势种群将不可避免地灭绝,伴随最优秀种群走向灭绝的种群依次还有第二、第三、第四强等的种群。同时将导致集合种群的强弱序由自然数的顺序规律演变为偶数种群强-奇数种群弱。  相似文献   

3.
集合种群动态对栖息地毁坏时空异质性的响应   总被引:3,自引:0,他引:3  
刘会玉  林振山  温腾 《生态学报》2007,27(9):3711-3717
栖息地毁坏既有时间异质性,也有空间异质性,而以往的研究往往只关注其中的一种。将两种不同的异质性共同引入到元胞自动机中,模拟了集合种群动态对栖息地毁坏时空异质性的响应。发现,在随机离散的栖息地毁坏下,由于物种的迁移繁殖力受栖息地毁坏的影响很大,迁移繁殖力弱而竞争力强的物种先灭绝。在连续的栖息地毁坏下,物种的迁移繁殖力受栖息地毁坏的影响较小,物种的灭绝由竞争力和迁移繁殖力共同决定:在有绝对优势种的群落里,种间竞争显著,弱物种先灭绝,而在没有绝对优势种的群落里,种间竞争较小,则以强物种先灭绝。因此,随机毁坏不利于强物种续存,而连续毁坏则不利于具有绝对优势种群的群落里的弱物种续存。在实际开发某一栖息地时,根据集合种群结构和被保护的对象采取相应的开发模式。  相似文献   

4.
集合种群具有与局域种群Allee效应相似的现象被称为似Allee效应.将似Allee效应引入2-竞争物种集合种群系统,建立了具有似Allee效应的2-物种集合种群演化动态模型.大量的数值模拟表明:(1)似Allee效应导致集合种群水平上两竞争物种构成的系统具有多个平衡态;(2)似Allee效应使竞争共存物种无法续存甚至全部灭绝,即使种群具有很高的初始斑块占有率,并且最终平衡态随初始斑块占有率变化而改变;(3)似Allee效应可能使竞争排斥物种共同灭绝,且效应越强,物种存活时间越短;但似Allee效应不会增强强物种对弱物种的排斥强度,反而可能使强物种变为弱物种,弱物种变为强物种,其具有与栖息地毁坏类似的影响种群竞争等级排序的作用;(4)似Allee效应对竞争集合种群续存是一个不稳定的干扰因素,微小的变化都将引起系统平衡态的剧变.但对于已经达到平衡态的集合种群系统,似Allee效应对强弱种群多度起到调节与制约的作用,有助于平衡态集合种群的稳定与共存,这一结论更完整的揭示了似Allee效应在竞争集合种群系统发展的不同阶段所起的不同作用.以上这些结论对物种保护及集合群落的管理具有重要的指导意义.  相似文献   

5.
集合种群动态对生境毁坏空间异质性的响应   总被引:2,自引:0,他引:2  
刘会玉  林振山  梁仁君  温腾 《生态学报》2007,27(8):3286-3293
首次将分形几何(Fractal geometry)与元胞自动机(Cellular automata)相结合,研究了破碎化生境中集合种群的空间分布格局动态,以及集合种群动态对生境毁坏空间异质性的响应。研究发现:(1)各个物种种群在生境中的分布具有很好的分形特征,物种的计盒维数(Box dimension)不仅可以很好地反映种群的空间分布结构,也能很好地反映种群动态。(2)如果将空间因素考虑进来的话,生境毁坏的灭绝债务(Time debt)将大于空间隐含模式所模拟的结果。(3)物种灭绝同时存在强物种灭绝和弱物种灭绝。并且只有在生境随机毁坏下,才与空间隐含的模拟结果比较接近,即强物种中将是最强物种率先灭绝。而在边缘毁坏这种比较集中成块的开发方式下,将是较强的物种灭绝。(4)边缘毁坏相对随机毁坏有利于物种,尤其是弱物种的长期续存。  相似文献   

6.
栖息地毁坏与动物物种灭绝关系的模拟研究   总被引:28,自引:13,他引:15  
林振山  汪曙光 《生态学报》2002,22(4):535-540
利用多个物种共存模式模拟了不同情况下的不同动物种群演化的动力学特性,研究结果表明:(1)由于栖息地的毁坏所导致的动手的种灭绝是依赖于对物种死亡率和有关平衡态的假设的,不同的假设下,既使栖息地的破坏率相同,灭绝的物种可能是竞争能力最强的若干物种,也可能是竞争能力相对较弱的若干物种,既不象传统的物种进化理论所认为的必是弱的物种先灭绝,也不象Tilman等人所认为的一定是最强的若干物种先灭绝;(2)如果弱的物种具有较高的平均死亡率,则当栖息地受到一定的毁坏时,将有较多强的物种灭绝,而且物种灭绝时间将大大缩短;(3)在物种死亡率不变的情形下,物种在未受毁坏栖息地上的平衡态和大占有率pl^0,将有利于物种的生存。  相似文献   

7.
物种灭绝对不同时间尺度人类活动的响应机制研究   总被引:2,自引:1,他引:1  
刘会玉  林振山 《生态学杂志》2005,24(10):1215-1220
通过修改Tilman的多物种共存的经典模式中栖息地毁坏率(D),使D随时间的推移呈线性增长情况下,本文模拟了百万年、万年和百年尺度人类活动对栖息地的破坏下,物种灭绝对栖息地毁坏的响应特征。结果表明,大时间尺度人类活动对栖息地毁坏导致物种的强弱关系发生变化,并且强物种先灭绝,而小时间尺度人类活动对栖息地破坏是弱物种先灭绝;在百万年和万年尺度上,物种对栖息地毁坏的响应是减幅振荡衰退直至灭绝,并且最强物种对栖息地的占有率(q)越大,振幅越大,而在百年尺度上,物种的演化几乎是直线衰退;在大时间尺度的栖息地毁坏情况下,q越大,则物种灭绝起始时间和所有物种灭绝的时间越长;而在较小的时间尺度的栖息地毁坏情况下,q越大,灭绝起始时间和所有物种最终灭绝的时间则越短。  相似文献   

8.
栖息地毁坏是物种多样性减少的首要因素之一, 因此研究物种演化对栖息地毁坏的响应是非常必要的。而栖息地的毁坏又有瞬间毁坏和持续毁坏两种, 以往对栖息地毁坏的研究集中在瞬间毁坏上, 而该文则是通过N种 竞争共存模型分析对比了物种演化对栖息地瞬间毁坏和持续毁坏的响应特征。研究发现 :不同性质的栖息地毁坏都会导致物种强弱关系的变化, 并非如通常所认为的强物种将免于遭受物种灭绝的威胁, 也不是强物种首先灭绝, 而是因集合种群结构的不同而异。在热带雨林群落, 瞬间毁坏下物种演化一般经历了强迫适应和恢复上升阶段, 而持续毁坏下物种得不到恢复, 只能持续衰退, 在较长一段时间内持续毁坏比瞬间毁坏更有利于物种的续存 ;而在温带森林群落, 瞬间毁坏下物种演化一般经历强迫适应, 恢复上升和准周期振荡, 最后平衡, 而持续毁坏下物种只能持续衰退, 出现了在栖息地持续毁坏率小于瞬间毁坏率时, 物种的栖息地占有率却小于瞬间毁坏时的占有率。  相似文献   

9.
基于栖息地恢复对群落不同种群演化影响的模拟   总被引:2,自引:2,他引:0  
通过建立基于栖息地恢复的多种群演化动力学模式,模拟了不同群落结构的不同物种种群的演化特点。模拟结果发现了两类灭绝机制,揭示了(1)小规模栖息地的恢复对群落中的弱小物种的影响是非常有限的,不会给弱小物种种群带来灭绝风险。大幅度的栖息地增加几乎使所有的物种种群都在最初数百年中内都有出现一定的增加,特别是竞争能力最强的物种,其幅度的增加最为显著,但次最强的物种种群可能会在千年左右灭绝。群落内幸存的种群将经历3个阶段迅速壮大(增加)阶段震荡阶段稳定阶段;(2)存在着协同现象,栖息地减少所导致种群的协同演化规律与栖息地恢复所导致的种群的演化规律两者之间既有共同点,又有不同点。毁坏是一种破坏,大规模的栖息地的恢复对已适应于破坏后新环境的某些物种也可能是一种威胁,这类似于生态入侵的初始阶段。  相似文献   

10.
不同生境毁坏速度下的物种灭绝机制   总被引:1,自引:0,他引:1  
刘会玉  林振山  温腾  梁仁君 《生态学报》2007,27(6):2410-2418
已有似Levins的多物种模型,在研究生境毁坏的影响时,一方面主要集中在对瞬间毁坏影响的研究,另一方面主要研究生境毁坏对强物种影响的研究。在Tilman的多物种竞争共存模型的基础上,同时考虑了生境毁坏直接效应和生境毁坏时间异质性,提出了全新的普适的多物种竞争共存的非自治动力模式。通过模拟物种灭绝对不同速度的生境毁坏时间异质性的响应发现:(1)物种灭绝既存在强物种由强到弱的灭绝,也存在弱物种由弱到强的灭绝。同时,弱物种灭绝机制进一步分为弱物种瞬间集体灭绝,以及较长时间由弱到强的灭绝。(2)生境毁坏速度越快,物种灭绝的时间越短,弱物种灭绝的越多,因此,生境毁坏速度越慢,越有利于弱物种的长期续存。(3)最强物种的多度越大,强-强物种抵御生境毁坏的能力越强,而弱-弱物种抵御生境毁坏的能力越弱,集体灭绝的弱-弱物种就越多。最强物种的多度大的群落(如温带森林),主要发生的是弱-弱物种灭绝,而最强物种多度小的群落(如热带雨林)同时发生强-强和弱-弱物种的灭绝。因此,争对不同结构的集合种群,不同的保护对象,应采取不同的管理策略。  相似文献   

11.
Habitat destruction, often caused by anthropogenic disturbance, can lead to the extinction of species at an unprecedented rate. It is important, therefore, to consider habitat destruction when assessing population viability. Another factor often ignored in population viability analysis, is the Allee effect that adds to the risk of populations already on the verge of extinction. Understanding the Allee effect on species dynamics and response to habitat destruction has intrinsic value in conservation prioritization. Here, the Allee effect was considered in a multi-species hierarchical competition model. Results showed that species persistence declines dramatically due to the Allee effect, and certain species become more susceptible to habitat destruction than others. Two extinction orders emerged under habitat destruction: either the best competitor becomes extinct first or the best colonizer first. The extinction debt and order, as well as the time lag between habitat destruction and species extinction, were found to be determined by species abundance and the intensity of the Allee effect.  相似文献   

12.
Invasive exotic species and habitat destruction are the major causes of biodiversity loss. Previous studies mostly focus on the effects of habitat fragmentation and dispersal abilities on invasion success. In this paper, the interactive effects of habitat destruction and competition have been studied by a multi-species model based on competition-dispersal trade-off. The results show that: 1) The interaction between native and exotic species can be direct competition as well as indirect facilitation.2) The extinction of native species caused by invasive species will proceed in order from best to poorest. 3) It is not always the superior competitor that invades successfully. 4) Habitat destruction can inhibit as well as promote invasion, which is decided by the interaction of habitat destruction and competition. So, the interaction of habitat destruction and competition should be taken into consideration when planning to control exotic invasion and to recover habitat. Moreover, it will be effective and efficient to protect and improve superior competitor next to exotic species for invasion control.  相似文献   

13.
破碎栖息地中物种灭绝机制   总被引:2,自引:0,他引:2  
刘会玉  林振山  孙燕  杨周  原艳梅 《生态学报》2008,28(8):3668-3674
栖息地毁坏既会直接降低物种多度,又会间接地降低物种迁移繁殖力,同时还会改变原有的种间平衡.尽管已有研究表明栖息地毁坏是物种灭绝的主要原因之一,但是尚未揭示破碎的栖息地中物种灭绝的驱动机制.通过元胞自动机模拟了物种灭绝对栖息地毁坏空间异质性响应的基础上,进一步研究了栖息地毁坏和种间竞争对物种灭绝的影响.结果发现:强物种的灭绝主要来自栖息地毁坏,而弱物种的灭绝,在随机毁坏下,主要由栖息地毁坏与种间竞争共同决定,而在边缘毁坏下则主要由种间竞争所引起的.栖息地毁坏与种间竞争共同引起的物种灭绝的时间非常短,而栖息地毁坏或种间竞争所引起的物种灭绝时间则较长.  相似文献   

14.
Human-caused habitat destruction, the major cause of species diversity losses, can be classified into two basic types, instantaneous destruction and continuous destruction. Thus, a universal model should be established to simulate and forecast the effects of different kinds of habitat destruction on species diversity during different historical periods. In this paper, we explore a multi-time-scale n-species model to study and compare species responses to instantaneous and continuous destruction. We find that (1) under instantaneous destruction, there are two different mechanisms of species extinction: one is a time-delayed deterministic extinction of superior competitors in order from the best to the poorest; the other is the extinction in a short time of inferior competitors. The survivors will experience three phases: decline, adjustment, and equilibrium. (2) When the total amounts of habitat destruction for both instantaneous and continuous cases are equal, the oscillation amplitudes of species abundances under instantaneous destruction are much greater than under continuous destruction, especially for inferior competitors, which make inferior competitors under instantaneous destruction more prone to stochastic extinction. Therefore instantaneous destruction is more detrimental to the survival of inferior competitors. (3) Under continuous destruction with habitat eventually being destroyed completely, there also are two types of species extinction mechanisms: the first is extinction in order from the best competitors to the poorest before complete destruction; the second is collective extinction due to complete destruction.  相似文献   

15.
Modern human-dominated landscapes are typically characterized by intensive land-use and high levels of habitat destruction, often resulting in sharply contrasted habitat mosaics. Fragmentation of remaining habitat is a major threat to biodiversity. In the present paper, we focus on the different features of habitat fragmentation. First we discuss the importance of pure habitat loss, fragment size, fragment isolation and quality, edge effects, and the importance of landscape structure. Second, we characterize life-history features of fragmentation-sensitive species, showing that rare, specialized, little dispersing species are most affected, as well as species characterized by high population variability and a high trophic position, while the effect of body size is unclear. Third, we discuss the conservation value of habitat fragments. The question arises how to relate studies on population survival to those of community structure and studies on biodiversity to those on ecologicalal functions. Despite the general superiority of large to small reserves, only small or medium-sized reserves are available in many human-dominated landscapes. A great number of small habitats covering a wide range of geographic area should maximize beta diversity and spreading of risk and may be very important for the regional conservation of biodiversity, in contrast to the prevailing arguments in favor of large habitats. Finally, landscape context influences community structure of fragments, and communities are composed of species that experience the landscape on a broad range of spatial scales. Spatial arrangement of habitat fragments in a landscape appears to be important only in simple, not complex landscapes.  相似文献   

16.
Population viability analysis is an important tool to assess the extinction risk in small populations of highly specialized primates. The blue‐eyed black lemur (Eulemur flavifrons) is critically endangered with a restricted range in the north‐western dry deciduous forest of Madagascar, where habitat fragmentation and loss of forest connectivity threaten its survival. We performed a population viability analysis (PVA) of this lemur in Ankarafa Forest in the Sahamalaza Peninsula National Park, north‐western Madagascar, to determine the demographic parameters most influential for population persistence and to assess extinction probabilities. We conducted PVA analyses using different demographic parameters which characterize the species including reproduction, lifespan and population size using the software VORTEX for six scenarios with 100 iterations and simulated over 100 years. The simulations suggested the first extinction within 13 years when the percentage of habitat destruction increased up to 12%. Severe habitat destruction such as fire and logging was the major cause which led to the risk of population extinction. Conservation strategies, in particular measures to reduce habitat destruction, are proposed to ensure the survival of this critically endangered lemur.  相似文献   

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