实现生态学与进化论的更紧密结合

IF 7.6 1区 环境科学与生态学 Q1 ECOLOGY Ecology Letters Pub Date : 2023-10-15 DOI:10.1111/ele.14298
Philippe Jarne, Gilles Pinay
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Significant efforts have indeed been made to percolate concepts and ideas between the two fields, especially across biodiversity levels (e.g. Hendry, <span>2017</span>; Leibold &amp; Chase, <span>2017</span>; Loreau, <span>2010</span>; Vellend, <span>2016</span>), even if (i) more has been done at the population to community level than for higher levels of ecological organization (e.g. including ecosystem functioning) and (ii) analyses of reciprocal feedbacks remain rare compared to mainstream research in either field.</p><p>The number of studies claiming to be ‘eco–evo’ has risen sharply (Bassar et al., <span>2021</span>), even if most of these studies actually represent classical ‘eco’ or ‘evo’ approaches, raising the question of what eco–evo really is. The definition proposed by Bassar et al. (<span>2021</span>; see also Hendry, <span>2017</span>, chapter 1) may serve as a baseline, built on the assumption that ecological and evolutionary processes occur at the same timescales because this allows for true eco-evolutionary dynamics (EED) and feedbacks. Fast global change (e.g. temperature increase; IPCC, <span>2023</span>) leading to enhanced selective pressure is certainly a good reason for considering such EED, highlighting the fact that fast evolutionary dynamics can match fast environmental change (and fast biodiversity loss; Diaz &amp; Malhi, <span>2022</span>). From this definition, the debate can (and must) develop to integrate concepts, ideas and practices of ecology and evolution into EED, and this is what is proposed in this <i>special issue</i> (general outline in Figure 1), revivifying this debate by considering several themes: the first relies on biodiversity itself, with the idea of including all biodiversity levels (from molecule to biomes), all branches of the tree of life, and some overlooked aspects of variability. The other themes are concerned with extending the temporal (and implicitly spatial) frame in which biodiversity unfolds, considering the full range of forces and processes acting on biodiversity, and lastly revisiting concepts and extending models.</p><p>Rather than commenting sequentially on each paper in this <i>special issue</i>, we have chosen a summary to gather the ideas and suggestions presented around these themes—all the more so as several articles contribute to multiple themes (Figure 1). They are not presented in order of importance, although some papers offer more general perspectives than others. Of course, this <i>special issue</i> does not exhaust the field of possibilities. Each paper suggests several avenues for further research, and we also mention (Conclusion) some additional research directions that are not considered here, but worth exploring.</p><p>The border between ecology and evolution is a vast domain, and this <i>special issue</i> of course did not explore it fully. Here, we sketch out a few further directions and themes that could fruitfully be pursued. First, technological tools (e.g. omics and environmental sensors/probes) used by evolutionary biologists and ecologists are serving as common objects for a dialogue between the two communities. Although they were not covered explicitly here, the idea runs through most papers of the <i>special issue</i>. Second, fitness is the currency used in evolutionary biology and energy that is used by the most functional parts of ecology. Rather abstract frameworks have been proposed to link fitness and energy (entropy) in evolutionary biology (e.g. Frank, <span>2009</span>). The approach of Brown et al. (<span>2018</span>), connecting energy use, traits and environment, is open to empirical evaluation, and might be pursued for understanding EED. Third, micro-organisms represent interactive interfaces between macro-organisms and their environment, which is encapsulated in the holobiont concept (Simon et al., <span>2019</span>). Both evolutionary and ecological paradigms are required to make sense of holobiont dynamics with echoes here in the contributions of Loreau et al. (<span>2010</span>) and Martiny et al. (<span>2023</span>), for example, on the notion of transmission units. Last, but not least, biodiversity management in a world of very fast and deleterious environmental changes should harness an eco-evolutionary framework and perspective (Sarrazin &amp; Leconte, <span>2016</span>), not only to manage the current problems but also to offer some hope for the future.</p><p>Both authors drafted and wrote the manuscript.</p><p>PJ has co-authored three papers in this <i>special issue</i> of <i>Ecology Letters</i>.</p>","PeriodicalId":161,"journal":{"name":"Ecology Letters","volume":"26 S1","pages":"S5-S10"},"PeriodicalIF":7.6000,"publicationDate":"2023-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ele.14298","citationCount":"0","resultStr":"{\"title\":\"Towards closer integration between ecology and evolution\",\"authors\":\"Philippe Jarne,&nbsp;Gilles Pinay\",\"doi\":\"10.1111/ele.14298\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Developing deeper links between ecology and evolution is not a new idea and has been advocating since at least the 1950s (Futuyma, <span>1986</span>), but most 20th-century attempts can be considered more as rapprochement than actual integration (Huneman, <span>2019</span> for a detailed historical review). However, based on early isolated insights (e.g. Antonovics, <span>1976</span>; Pimentel, <span>1961</span>), the idea has been revivified over the last two decades, around the concepts of eco-evolutionary dynamics and feedbacks (Hendry, <span>2017</span>). Significant efforts have indeed been made to percolate concepts and ideas between the two fields, especially across biodiversity levels (e.g. Hendry, <span>2017</span>; Leibold &amp; Chase, <span>2017</span>; Loreau, <span>2010</span>; Vellend, <span>2016</span>), even if (i) more has been done at the population to community level than for higher levels of ecological organization (e.g. including ecosystem functioning) and (ii) analyses of reciprocal feedbacks remain rare compared to mainstream research in either field.</p><p>The number of studies claiming to be ‘eco–evo’ has risen sharply (Bassar et al., <span>2021</span>), even if most of these studies actually represent classical ‘eco’ or ‘evo’ approaches, raising the question of what eco–evo really is. The definition proposed by Bassar et al. (<span>2021</span>; see also Hendry, <span>2017</span>, chapter 1) may serve as a baseline, built on the assumption that ecological and evolutionary processes occur at the same timescales because this allows for true eco-evolutionary dynamics (EED) and feedbacks. Fast global change (e.g. temperature increase; IPCC, <span>2023</span>) leading to enhanced selective pressure is certainly a good reason for considering such EED, highlighting the fact that fast evolutionary dynamics can match fast environmental change (and fast biodiversity loss; Diaz &amp; Malhi, <span>2022</span>). From this definition, the debate can (and must) develop to integrate concepts, ideas and practices of ecology and evolution into EED, and this is what is proposed in this <i>special issue</i> (general outline in Figure 1), revivifying this debate by considering several themes: the first relies on biodiversity itself, with the idea of including all biodiversity levels (from molecule to biomes), all branches of the tree of life, and some overlooked aspects of variability. The other themes are concerned with extending the temporal (and implicitly spatial) frame in which biodiversity unfolds, considering the full range of forces and processes acting on biodiversity, and lastly revisiting concepts and extending models.</p><p>Rather than commenting sequentially on each paper in this <i>special issue</i>, we have chosen a summary to gather the ideas and suggestions presented around these themes—all the more so as several articles contribute to multiple themes (Figure 1). They are not presented in order of importance, although some papers offer more general perspectives than others. Of course, this <i>special issue</i> does not exhaust the field of possibilities. Each paper suggests several avenues for further research, and we also mention (Conclusion) some additional research directions that are not considered here, but worth exploring.</p><p>The border between ecology and evolution is a vast domain, and this <i>special issue</i> of course did not explore it fully. Here, we sketch out a few further directions and themes that could fruitfully be pursued. First, technological tools (e.g. omics and environmental sensors/probes) used by evolutionary biologists and ecologists are serving as common objects for a dialogue between the two communities. Although they were not covered explicitly here, the idea runs through most papers of the <i>special issue</i>. Second, fitness is the currency used in evolutionary biology and energy that is used by the most functional parts of ecology. Rather abstract frameworks have been proposed to link fitness and energy (entropy) in evolutionary biology (e.g. Frank, <span>2009</span>). The approach of Brown et al. (<span>2018</span>), connecting energy use, traits and environment, is open to empirical evaluation, and might be pursued for understanding EED. Third, micro-organisms represent interactive interfaces between macro-organisms and their environment, which is encapsulated in the holobiont concept (Simon et al., <span>2019</span>). Both evolutionary and ecological paradigms are required to make sense of holobiont dynamics with echoes here in the contributions of Loreau et al. (<span>2010</span>) and Martiny et al. (<span>2023</span>), for example, on the notion of transmission units. 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引用次数: 0

摘要

在生态学和进化论之间建立更深层次的联系并不是一个新想法,至少从20世纪50年代起就一直在提倡(Futuyma,1986),但20世纪的大多数尝试更多地可以被视为和解,而不是实际的融合(Huneman,2019,详细历史回顾)。然而,基于早期孤立的见解(例如Antonovics,1976;Pimentel,1961),这一想法在过去二十年中围绕生态进化动力学和反馈的概念得到了复兴(Hendry,2017)。确实已经做出了重大努力来在这两个领域之间渗透概念和思想,特别是在生物多样性层面上(例如,Hendry,2017;Leibold和Chase,2017;Loreau,2010;Vellend,2016),即使(i)在群体到社区层面上比在更高层次的生态组织(例如,包括生态系统功能)上做得更多,以及(ii)与任何一个领域的主流研究相比,对相互反馈的分析仍然很少。声称“eco-evo”的研究数量急剧增加(Bassar等人,2021),即使这些研究中的大多数实际上代表了经典的“eco”或“evo”方法,也提出了什么是eco-evo的问题。Bassar等人提出的定义。(2021;另见Hendry,2017,第1章)可以作为基线,建立在生态和进化过程发生在相同时间尺度的假设之上,因为这允许真正的生态进化动力学(EED)和反馈。全球快速变化(例如,温度升高;IPCC,2023)导致选择性压力增强,这无疑是考虑这种EED的一个很好的理由,强调了快速进化动力学可以与快速环境变化(以及快速生物多样性丧失)相匹配的事实;Diaz和Malhi,2022)。根据这一定义,辩论可以(也必须)将生态学和进化的概念、思想和实践整合到EED中,这就是本特刊中提出的(图1中的概要),通过考虑几个主题来振兴这场辩论:第一个主题依赖于生物多样性本身,其理念是包括所有生物多样性水平(从分子到生物群落),生命之树的所有分支,以及一些被忽视的可变性方面。其他主题涉及扩展生物多样性展开的时间(和隐含的空间)框架,考虑作用于生物多样性的各种力量和过程,最后重新审视概念和扩展模型。我们没有按顺序评论本期特刊中的每一篇论文,而是选择了一个摘要来收集围绕这些主题提出的想法和建议——尤其是几篇文章对多个主题做出了贡献(图1)。它们没有按重要性顺序排列,尽管有些论文比其他论文提供了更普遍的观点。当然,这期特刊并没有穷尽各种可能性。每一篇论文都提出了几条进一步研究的途径,我们还提到了(结论)一些额外的研究方向,这些方向在这里没有考虑,但值得探索。生态学和进化论之间的边界是一个广阔的领域,而这本特刊当然没有充分探讨它。在这里,我们勾勒出一些可以卓有成效地追求的进一步方向和主题。首先,进化生物学家和生态学家使用的技术工具(如组学和环境传感器/探针)是两个群体之间对话的共同对象。尽管这里没有明确提及,但这一想法贯穿了特刊的大多数论文。其次,适应度是进化生物学中使用的货币,也是生态学中最具功能部分使用的能量。在进化生物学中,已经提出了相当抽象的框架来连接适应度和能量(熵)(例如Frank,2009)。Brown等人(2018)的方法,将能源使用、特性和环境联系起来,对实证评估持开放态度,并可能用于理解EED。第三,微生物代表了宏观生物与其环境之间的互动界面,这体现在全生物概念中(Simon et al.,2019)。进化和生态学范式都需要理解全生物动力学,这与Loreau et al.(2010)和Martiny et al.(2023)的贡献相呼应。例如,关于传输单元的概念。最后,但并非最不重要的是,在一个环境变化非常迅速和有害的世界里,生物多样性管理应该利用生态进化框架和视角(Sarrazin&;Leconte,2016),不仅要管理当前的问题,还要为未来带来一些希望。两位作者起草并撰写了手稿。PJ在《生态学快报》特刊上与人合著了三篇论文。
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Towards closer integration between ecology and evolution

Developing deeper links between ecology and evolution is not a new idea and has been advocating since at least the 1950s (Futuyma, 1986), but most 20th-century attempts can be considered more as rapprochement than actual integration (Huneman, 2019 for a detailed historical review). However, based on early isolated insights (e.g. Antonovics, 1976; Pimentel, 1961), the idea has been revivified over the last two decades, around the concepts of eco-evolutionary dynamics and feedbacks (Hendry, 2017). Significant efforts have indeed been made to percolate concepts and ideas between the two fields, especially across biodiversity levels (e.g. Hendry, 2017; Leibold & Chase, 2017; Loreau, 2010; Vellend, 2016), even if (i) more has been done at the population to community level than for higher levels of ecological organization (e.g. including ecosystem functioning) and (ii) analyses of reciprocal feedbacks remain rare compared to mainstream research in either field.

The number of studies claiming to be ‘eco–evo’ has risen sharply (Bassar et al., 2021), even if most of these studies actually represent classical ‘eco’ or ‘evo’ approaches, raising the question of what eco–evo really is. The definition proposed by Bassar et al. (2021; see also Hendry, 2017, chapter 1) may serve as a baseline, built on the assumption that ecological and evolutionary processes occur at the same timescales because this allows for true eco-evolutionary dynamics (EED) and feedbacks. Fast global change (e.g. temperature increase; IPCC, 2023) leading to enhanced selective pressure is certainly a good reason for considering such EED, highlighting the fact that fast evolutionary dynamics can match fast environmental change (and fast biodiversity loss; Diaz & Malhi, 2022). From this definition, the debate can (and must) develop to integrate concepts, ideas and practices of ecology and evolution into EED, and this is what is proposed in this special issue (general outline in Figure 1), revivifying this debate by considering several themes: the first relies on biodiversity itself, with the idea of including all biodiversity levels (from molecule to biomes), all branches of the tree of life, and some overlooked aspects of variability. The other themes are concerned with extending the temporal (and implicitly spatial) frame in which biodiversity unfolds, considering the full range of forces and processes acting on biodiversity, and lastly revisiting concepts and extending models.

Rather than commenting sequentially on each paper in this special issue, we have chosen a summary to gather the ideas and suggestions presented around these themes—all the more so as several articles contribute to multiple themes (Figure 1). They are not presented in order of importance, although some papers offer more general perspectives than others. Of course, this special issue does not exhaust the field of possibilities. Each paper suggests several avenues for further research, and we also mention (Conclusion) some additional research directions that are not considered here, but worth exploring.

The border between ecology and evolution is a vast domain, and this special issue of course did not explore it fully. Here, we sketch out a few further directions and themes that could fruitfully be pursued. First, technological tools (e.g. omics and environmental sensors/probes) used by evolutionary biologists and ecologists are serving as common objects for a dialogue between the two communities. Although they were not covered explicitly here, the idea runs through most papers of the special issue. Second, fitness is the currency used in evolutionary biology and energy that is used by the most functional parts of ecology. Rather abstract frameworks have been proposed to link fitness and energy (entropy) in evolutionary biology (e.g. Frank, 2009). The approach of Brown et al. (2018), connecting energy use, traits and environment, is open to empirical evaluation, and might be pursued for understanding EED. Third, micro-organisms represent interactive interfaces between macro-organisms and their environment, which is encapsulated in the holobiont concept (Simon et al., 2019). Both evolutionary and ecological paradigms are required to make sense of holobiont dynamics with echoes here in the contributions of Loreau et al. (2010) and Martiny et al. (2023), for example, on the notion of transmission units. Last, but not least, biodiversity management in a world of very fast and deleterious environmental changes should harness an eco-evolutionary framework and perspective (Sarrazin & Leconte, 2016), not only to manage the current problems but also to offer some hope for the future.

Both authors drafted and wrote the manuscript.

PJ has co-authored three papers in this special issue of Ecology Letters.

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来源期刊
Ecology Letters
Ecology Letters 环境科学-生态学
CiteScore
17.60
自引率
3.40%
发文量
201
审稿时长
1.8 months
期刊介绍: Ecology Letters serves as a platform for the rapid publication of innovative research in ecology. It considers manuscripts across all taxa, biomes, and geographic regions, prioritizing papers that investigate clearly stated hypotheses. The journal publishes concise papers of high originality and general interest, contributing to new developments in ecology. Purely descriptive papers and those that only confirm or extend previous results are discouraged.
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