海岛的生态和进化动态。

IF 11 1区 生物学 Q1 BIOLOGY
Bram Vanschoenwinkel, Luiza F A de Paula, Joren M Snoeks, Tom Van der Stocken, Falko T Buschke, Stefan Porembski, Fernando A O Silveira
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引用次数: 0

摘要

岛屿是生态学、生物地理学和进化生物学的基本模式系统。然而,与水生岛屿不同,陆生岛屿受到的关注相对较少。在这些陆地岛屿中,海岛(即岩性各异、地势不高的孤立岩石露头)最为突出,是分布于全球各生物群落的标志性实例。由于其岩性持久,海岛变化缓慢,可持续数千万年。在这篇综述中,我们提出了海岛山的生物学定义,该定义从生物群的角度抓住了海岛山的三个基本特征。这三个基本特征是年代久远、与世隔绝以及存在独特的微生境,而这些微生境在周围基质中是罕见的或不存在的,从而形成了独特的群落,这些群落通常具有独特和特有的生物区系。我们综合了目前的研究成果,提出了一系列可检验的假设,以加深我们对日益受到人为威胁的海岛多样性的起源和维持的理解。通过提供与周围栖息地不同的栖息地(如旱地景观中的潮湿微生境和潮湿热带景观中的干旱环境),海岛可能会使特定的品系在其典型的地理范围之外繁衍生息。特别是在旱地和退化地貌中,石岛不仅可以提供不同的栖息地,还可以作为生态庇护所或进化庇护所,提供比周围基质更广泛的潜在微生境,增强复原力,促进区域生物多样性。基质的核心作用确保了海岛的生态和进化动态有别于海洋岛屿等真正意义上的岛屿。由于海岛生物群落与陆地基质共存,海岛生物群落与基质生物群落之间的相互作用会对彼此产生重大影响。在进化的时间尺度上,基质物种可能会收缩到岛山避难所,从而保留了世系,而隔离和重新连接的周期可能会通过物种泵推动物种的分化。尽管人们主要从岛屿生物地理学的角度来研究海岛生物多样性,但我们认为,根据所考虑的生物的空间尺度、栖息地特异性和流动性,一系列不同的理论和范式可以帮助解释不同分类和功能的海岛物种群的生物地理学和当地分布模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The ecological and evolutionary dynamics of inselbergs.

Islands are fundamental model systems in ecology, biogeography, and evolutionary biology. However, terrestrial islands, unlike their aquatic counterparts, have received comparatively less attention. Among these land islands, inselbergs (i.e. isolated rock outcrops with diverse lithologies and a modest topographical prominence) stand out as iconic examples distributed worldwide across global biomes. Due to their durable lithology, inselbergs change slowly, persisting for tens of millions of years. In this review, we propose a biological definition for inselbergs that captures three fundamental characteristics of inselbergs from the perspective of biota. These are old age, isolation and the presence of unique microhabitats that are rare or absent in the surrounding matrix, fostering distinct communities often with unique and endemic biota. We synthesise the state of the art and formulate a set of testable hypotheses to deepen our understanding of the origins and maintenance of diversity on inselbergs, which are increasingly exposed to anthropogenic threats. By offering different habitats compared to the surrounding habitat matrix (e.g. moist microhabitats in dryland landscapes and xeric environments in humid tropical landscapes), inselbergs may allow specific lineages to thrive beyond their typical geographical limits. Particularly in drylands and degraded landscapes, inselbergs may not just provide different habitats but also act as ecological refuges or evolutionary refugia by providing a wider range of potential microhabitats than the surrounding matrix, enhancing resilience and promoting regional biodiversity. The central role of the matrix ensures that the ecological and evolutionary dynamics of inselbergs differ from those of true islands such as oceanic islands. Given that inselberg biota coexist within a terrestrial matrix, interactions between inselberg and matrix populations impact each other significantly. Over evolutionary timescales, matrix species may contract to inselberg refugia, preserving lineages while cycles of isolation and reconnection may drive speciation via a species pump. Although inselberg biodiversity has been studied predominantly from an island biogeography perspective, we argue that depending on the spatial scale, habitat specificity and mobility of the organisms considered, a range of different theories and paradigms can help explain the biogeography and local distribution patterns of different taxonomic and functional groups of inselberg species.

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来源期刊
Biological Reviews
Biological Reviews 生物-生物学
CiteScore
21.30
自引率
2.00%
发文量
99
审稿时长
6-12 weeks
期刊介绍: Biological Reviews is a scientific journal that covers a wide range of topics in the biological sciences. It publishes several review articles per issue, which are aimed at both non-specialist biologists and researchers in the field. The articles are scholarly and include extensive bibliographies. Authors are instructed to be aware of the diverse readership and write their articles accordingly. The reviews in Biological Reviews serve as comprehensive introductions to specific fields, presenting the current state of the art and highlighting gaps in knowledge. Each article can be up to 20,000 words long and includes an abstract, a thorough introduction, and a statement of conclusions. The journal focuses on publishing synthetic reviews, which are based on existing literature and address important biological questions. These reviews are interesting to a broad readership and are timely, often related to fast-moving fields or new discoveries. A key aspect of a synthetic review is that it goes beyond simply compiling information and instead analyzes the collected data to create a new theoretical or conceptual framework that can significantly impact the field. Biological Reviews is abstracted and indexed in various databases, including Abstracts on Hygiene & Communicable Diseases, Academic Search, AgBiotech News & Information, AgBiotechNet, AGRICOLA Database, GeoRef, Global Health, SCOPUS, Weed Abstracts, and Reaction Citation Index, among others.
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