Landscape Structure Affects Metapopulation-Scale Tipping Points.

IF 2.4 2区 环境科学与生态学 Q2 ECOLOGY
American Naturalist Pub Date : 2023-07-01 Epub Date: 2023-05-31 DOI:10.1086/724550
Camille Saade, Emanuel A Fronhofer, Benoît Pichon, Sonia Kéfi
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引用次数: 1

Abstract

AbstractEven when environments deteriorate gradually, ecosystems may shift abruptly from one state to another. Such catastrophic shifts are difficult to predict and sometimes to reverse (so-called hysteresis). While well studied in simplified contexts, we lack a general understanding of how catastrophic shifts spread in realistically spatially structured landscapes. For different types of landscape structures, including typical terrestrial modular and riverine dendritic networks, we here investigate landscape-scale stability in metapopulations whose patches can locally exhibit catastrophic shifts. We find that such metapopulations usually exhibit large-scale catastrophic shifts and hysteresis and that the properties of these shifts depend strongly on the metapopulation spatial structure and on the population dispersal rate: an intermediate dispersal rate, a low average degree, or a riverine spatial structure can largely reduce hysteresis size. Our study suggests that large-scale restoration is easier with spatially clustered restoration efforts and in populations characterized by an intermediate dispersal rate.

景观结构影响超人口规模引爆点。
即使环境逐渐恶化,生态系统也可能突然从一种状态转变为另一种状态。这种灾难性的转变很难预测,有时也很难逆转(所谓的滞后性)。虽然在简化的背景下得到了很好的研究,但我们缺乏对灾难性变化如何在现实空间结构景观中传播的一般理解。对于不同类型的景观结构,包括典型的陆地模块化和河流树突状网络,我们在这里研究景观尺度稳定性的元种群,其斑块可以局部表现出灾难性的变化。研究发现,这类超种群通常表现出大规模的灾难性迁移和滞后性,而这些迁移的性质在很大程度上取决于超种群的空间结构和种群的扩散率:中等的扩散率、较低的平均程度或河流空间结构可以很大程度上减小滞后性的大小。我们的研究表明,在空间聚集的恢复努力和以中等分散率为特征的种群中,大规模恢复更容易。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
American Naturalist
American Naturalist 环境科学-进化生物学
CiteScore
5.40
自引率
3.40%
发文量
194
审稿时长
3 months
期刊介绍: Since its inception in 1867, The American Naturalist has maintained its position as one of the world''s premier peer-reviewed publications in ecology, evolution, and behavior research. Its goals are to publish articles that are of broad interest to the readership, pose new and significant problems, introduce novel subjects, develop conceptual unification, and change the way people think. AmNat emphasizes sophisticated methodologies and innovative theoretical syntheses—all in an effort to advance the knowledge of organic evolution and other broad biological principles.
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