{"title":"2016 Julie S Denslow & Peter Ashton Prizes for the Outstanding Articles Published in Biotropica","authors":"","doi":"10.1111/btp.12414","DOIUrl":null,"url":null,"abstract":"<p><span>Every year <i>Biotropica</i></span>’<span>s Editorial Board selects two outstanding papers published in our journal</span> in the previous calendar year as the recipients of the <b>Denslow</b> and <b>Ashton Prizes</b>. Criteria for selecting the papers to receive these awards include clarity of presentation, a strong basis in natural history, well-planned experimental or sampling design, and the novel insights gained into critical processes that influence the structure, functioning, or conservation of tropical systems. Below the authors of the award-winning articles describe what motivated their studies and how they hope the work will inspire other researchers; we hope you enjoy these insights into the process that resulted in such novel and interesting work and ask that you join <i>Biotropica</i>'s Editorial Board and The Association for Tropical Biology and Conservation in congratulating the honorees.</p><p><b>Emilio M. Bruna,</b> Editor-in-Chief</p><p>University of Florida, USA</p><p><b>Julie S. Denslow Prize for the Outstanding Paper in <i>Biotropica</i>:</b> Yoshinori Nakazawa and Andrew Townsend Peterson. 2015. <i>Effects of Climate History and Environmental Grain on Species’ Distributions in Africa and South America</i>. <i>Biotropica</i>, 47: 292–299.</p><p><span>Nakazawa and Peterson</span> (<span>2015</span>) <span>presented a series of analyses of how simple sets of processes</span>,<span> such as ecological niche requirements</span>, real-world landscapes, and changing climates, act to generate patterns of biodiversity. This work is predicated on sampling environments across Africa and South America, and assessing their stability through the last two major climate shifts at the end of the Pleistocene. This contribution adds to a growing body of research that gets at how biodiversity patterns may be generated.</p><p>The literature regarding biodiversity patterns at global and regional scales frequently invokes or explores diverse biotic and abiotic mechanisms that may generate those patterns, including energy availability, interspecific interactions, species packing, speciation–extinction balance, etc. (Gaston <span>2000</span>, Willig <i>et al</i>. <span>2003</span>, Ricklefs <span>2004</span>, Orme <i>et al</i>. <span>2006</span>, Storch <i>et al</i>. <span>2006</span>). Different authors assessing different taxa in different geographic contexts invariably emphasize different causal factors. A recent paper by an impressive list of authors recently sketched a “general simulation model” that would include each of the relevant factors in an overall simulation framework and that would allow exploration of important drivers (Gotelli <i>et al</i>. <span>2009</span>), although this model has not, apparently, been implemented as of yet.</p><p>More generally, this body of work began with novel analyses by Robert Colwell and Thiago Rangel (Rangel <i>et al</i>. <span>2007</span>), which explored models of biodiversity and biogeography, based on range fragmentation, speciation, and extinction processes, and emphasized abiotic niche characteristics as key drivers of biodiversity patterns. Further recent work (Kleidon <i>et al</i>. <span>2009</span>, Reu <i>et al</i>. <span>2011</span>) explored the survivability of ‘species’ using a diversity of niche characteristics, and again discovered a crucial role of tolerances of abiotic conditions in determining how much biological diversity can be maintained at a site. These initial steps laid a foundation of insights that suggested that realistic biodiversity patterns could be generated from simple processes not requiring complex explanations based on community interactions.</p><p>Nakazawa (<span>2013</span>) explored suites of factors that could explain the present-day biodiversity pattern across South America. This study supported climate, seasonal variability, and river barriers as jointly required to approximate present-day patterns. Nakazawa and Peterson (<span>2015</span>) added a further dimension to these questions: global-scale climate changes over the end of the Pleistocene, from the warm Last Interglacial period, through the cool Last Glacial Maximum, to the warm present-day conditions. Based on simple assumptions about dispersal potential and persistence of species, they developed a subtractive view (<i>i.e</i>., if species existed at a place, would they survive the last glacial cycle of the Pleistocene?) of biodiversity patterns across South America and Africa. That is, stability in environments in Africa in this period was markedly lower than that in South America. These differences created marked contrasts between the two continents in simulated extinction rates that approximate real-world differences in forest biodiversity.</p><p>This suite of explorations by various researchers has suggested a set of ‘next steps’: a simulation environment that permits assessment of the number of processes necessary to explain the major features of global biodiversity pattern. A general simulation model similar to that envisioned by Gotelli <i>et al</i>. (<span>2009</span>) has been developed and implemented across Eurasia, to assess the relative roles of niche breadth, dispersal, and rates of environmental change, in driving speciation and extinction (Qiao <i>et al</i>. <span>2016</span>). This model is now being extended to include more realistic climate dynamics, and landscapes and environments worldwide. The goal is to assess the degree to which global biodiversity patterns are explained without the need to appeal to biotic interactions—for example, what is the balance of historical versus current ecological factors in driving diversity patterns? The answers to such questions must await considerable additional exploration and testing, but, positively, frameworks to answer them with appropriate spatiotemporal scales and extents are now being explored.</p><p>\n <b>Yoshinori Nakazawa</b>\n </p><p>\n <i>Disease Ecologist, Centers for Disease Control and Prevention, Atlanta, Georgia, USA</i>\n </p><p>\n <b>A. Townsend Peterson</b>\n </p><p>\n <i>University Distinguished Professor, Biodiversity Institute and Department of Ecology and Evolutionary Biology, University of Kansas, Lawrence, Kansas, USA</i>\n </p><p><b>Peter Ashton Prize for the Outstanding Paper in </b><i><b>Biotropica</b></i> <b>by a Student:</b> Franziska Peter, Dana G. Berens, Graham R. Grieve and Nina Farwig. 2015. <i>Forest Fragmentation Drives the Loss of Insectivorous Birds and an Associated Increase in Herbivory</i>. <i>Biotropica</i>, 47: 626–635.</p><p><span>My first experience with comprehensive ecological field studies was during my diploma thesis</span>. Under the supervision of Prof. Dr. Tim Diekötter and Dr. Frank Jauker I studied the effects of oilseed rape and semi-natural habitats on pollinator communities and related ecosystem services in a temperate agricultural landscape matrix. Findings were highly complex as pollinator responses were species-specific (with respect to social and nesting behavior as well as morphological traits) and showed temporal and spatial variability. Furthermore, I became aware of the strong and multifaceted consequences of human-driven land-use changes—ranging from the sheer loss of species and shifts in the composition of pollinator communities to cruel things such as ‘nectar robbing’ as well as reduced reproductive success of wild bees and associated wild plants.</p><p>Following my diploma thesis, I was excited when Prof. Dr. Nina Farwig welcomed me in her working group. With the PhD position I was given the opportunity to complement my knowledge on effects of human-driven land-use changes on trophic interactions by adding antagonistic plant–herbivore and predator–prey interactions in diverse and structurally complex subtropical forest ecosystems. Being part of a keen research team (supported by the Robert Bosch Stiftung) focusing on the impact of numerous anthropogenic drivers on biotic communities and related ecological processes and ecosystem functioning I could not await the following years. My excitement grew when I first visited South Africa and the previously established study region located at the Oribi Gorge Nature Reserve in southern KwaZulu-Natal. I was astonished by the overwhelming diversity of animal and plant species. Having no experience with subtropical ecosystems it took me a few weeks to be able to identify the majority of tree species within unmanaged rather indigenous forests. However, particularly the fascination about the infinite biodiversity drove me to improve species knowledge, grow expertise for complex trophic interactions in highly diverse forests and fuelled my enthusiasm for fieldwork. As a result, fieldwork, broadening my knowledge in landscape and conservation ecology, daily encounters with wildlife, being integrated in a highly motivated research group as well as the local South African community created an unforgettable experience. A number of South Africans (e.g., Ezemvelo KZN Wildlife, scientists, local farmers) supported and contributed to our work due to their close relationship with nature and their awareness of the value of their highly diverse environment.</p><p>I did two subsequent field studies and the nomination of the latter study for Biotropica's Ashton Prize is of great honor to me and my co-authors. The first study focused on main and interactive effects of forest fragmentation and tree diversity on plant–herbivore interactions. In brief, findings of this study revealed that effects of local tree diversity on plant–herbivore interactions diminished with increasing forest fragmentation on the landscape scale. With the second study I aimed to build on previous research that investigated effects of habitat fragmentation on either plant–herbivore or predator–prey interactions. In particular, I was curious whether forest fragmentation triggers cascades across multitrophic interactions and changes patterns in ecosystem functioning. Hence, I simultaneously monitored bird communities, insect herbivore abundances as well as leaf area loss along an increasing degree of forest fragmentation. I quantified the trophic control of herbivorous insects by insectivorous birds through bird exclosures attached to the common tree species <i>Englerophytum natalensis</i>. Installing the bird exclosure and the control at the same plant individual enabled me to exclude confounding effects of the microhabitat and the individual plant history and thus, to focus on the impact of forest fragmentation on plant–herbivore interactions through changes in the local bird community. Findings offered insights into complex effects of forest fragmentation on multitrophic interactions. Both forest fragmentation and vegetation heterogeneity structured the functional composition of bird communities as a result of species-specific forest-dependency and resource requirements as well as preferences for structural forest habitat features. As a consequence, open-habitat omnivorous birds seemed to benefit from forest fragmentation while abundances of forest-dependent insectivorous birds decreased with increasing forest fragmentation. However, I found no significant difference in the abundance of herbivorous insects within the bird exclosure relative to the control which may be explained by the restriction to a rather seasonal ‘snapshot’ of the insect herbivore community. In fact, leaf area loss which accumulated during the study period was higher when birds were excluded supporting the functional role of insectivorous birds for the natural control of herbivorous insects. Finally, the increase in leaf area loss for the control branches with increasing forest fragmentation implies that increasing forest fragmentation diminished the natural control of herbivorous insects by insectivorous birds.</p><p>Overall, findings of my study show that forest fragmentation in fact seems to trigger cascades across multitrophic interactions and ultimately, may hamper ecosystem functioning. Therefore, the application of multitrophic approaches offers new insights into the comprehensive impact of anthropogenic drivers and enables to discover changes in ecological processes and thus, ecosystem functioning. In addition, results support previous studies that concluded that the protection and connectivity of preferably large forest habitats benefits ecosystem functioning.</p>","PeriodicalId":8982,"journal":{"name":"Biotropica","volume":"48 6","pages":"930-932"},"PeriodicalIF":1.8000,"publicationDate":"2016-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1111/btp.12414","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biotropica","FirstCategoryId":"93","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/btp.12414","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ECOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Every year Biotropica’s Editorial Board selects two outstanding papers published in our journal in the previous calendar year as the recipients of the Denslow and Ashton Prizes. Criteria for selecting the papers to receive these awards include clarity of presentation, a strong basis in natural history, well-planned experimental or sampling design, and the novel insights gained into critical processes that influence the structure, functioning, or conservation of tropical systems. Below the authors of the award-winning articles describe what motivated their studies and how they hope the work will inspire other researchers; we hope you enjoy these insights into the process that resulted in such novel and interesting work and ask that you join Biotropica's Editorial Board and The Association for Tropical Biology and Conservation in congratulating the honorees.
Emilio M. Bruna, Editor-in-Chief
University of Florida, USA
Julie S. Denslow Prize for the Outstanding Paper in Biotropica: Yoshinori Nakazawa and Andrew Townsend Peterson. 2015. Effects of Climate History and Environmental Grain on Species’ Distributions in Africa and South America. Biotropica, 47: 292–299.
Nakazawa and Peterson (2015) presented a series of analyses of how simple sets of processes, such as ecological niche requirements, real-world landscapes, and changing climates, act to generate patterns of biodiversity. This work is predicated on sampling environments across Africa and South America, and assessing their stability through the last two major climate shifts at the end of the Pleistocene. This contribution adds to a growing body of research that gets at how biodiversity patterns may be generated.
The literature regarding biodiversity patterns at global and regional scales frequently invokes or explores diverse biotic and abiotic mechanisms that may generate those patterns, including energy availability, interspecific interactions, species packing, speciation–extinction balance, etc. (Gaston 2000, Willig et al. 2003, Ricklefs 2004, Orme et al. 2006, Storch et al. 2006). Different authors assessing different taxa in different geographic contexts invariably emphasize different causal factors. A recent paper by an impressive list of authors recently sketched a “general simulation model” that would include each of the relevant factors in an overall simulation framework and that would allow exploration of important drivers (Gotelli et al. 2009), although this model has not, apparently, been implemented as of yet.
More generally, this body of work began with novel analyses by Robert Colwell and Thiago Rangel (Rangel et al. 2007), which explored models of biodiversity and biogeography, based on range fragmentation, speciation, and extinction processes, and emphasized abiotic niche characteristics as key drivers of biodiversity patterns. Further recent work (Kleidon et al. 2009, Reu et al. 2011) explored the survivability of ‘species’ using a diversity of niche characteristics, and again discovered a crucial role of tolerances of abiotic conditions in determining how much biological diversity can be maintained at a site. These initial steps laid a foundation of insights that suggested that realistic biodiversity patterns could be generated from simple processes not requiring complex explanations based on community interactions.
Nakazawa (2013) explored suites of factors that could explain the present-day biodiversity pattern across South America. This study supported climate, seasonal variability, and river barriers as jointly required to approximate present-day patterns. Nakazawa and Peterson (2015) added a further dimension to these questions: global-scale climate changes over the end of the Pleistocene, from the warm Last Interglacial period, through the cool Last Glacial Maximum, to the warm present-day conditions. Based on simple assumptions about dispersal potential and persistence of species, they developed a subtractive view (i.e., if species existed at a place, would they survive the last glacial cycle of the Pleistocene?) of biodiversity patterns across South America and Africa. That is, stability in environments in Africa in this period was markedly lower than that in South America. These differences created marked contrasts between the two continents in simulated extinction rates that approximate real-world differences in forest biodiversity.
This suite of explorations by various researchers has suggested a set of ‘next steps’: a simulation environment that permits assessment of the number of processes necessary to explain the major features of global biodiversity pattern. A general simulation model similar to that envisioned by Gotelli et al. (2009) has been developed and implemented across Eurasia, to assess the relative roles of niche breadth, dispersal, and rates of environmental change, in driving speciation and extinction (Qiao et al. 2016). This model is now being extended to include more realistic climate dynamics, and landscapes and environments worldwide. The goal is to assess the degree to which global biodiversity patterns are explained without the need to appeal to biotic interactions—for example, what is the balance of historical versus current ecological factors in driving diversity patterns? The answers to such questions must await considerable additional exploration and testing, but, positively, frameworks to answer them with appropriate spatiotemporal scales and extents are now being explored.
Yoshinori Nakazawa
Disease Ecologist, Centers for Disease Control and Prevention, Atlanta, Georgia, USA
A. Townsend Peterson
University Distinguished Professor, Biodiversity Institute and Department of Ecology and Evolutionary Biology, University of Kansas, Lawrence, Kansas, USA
Peter Ashton Prize for the Outstanding Paper in Biotropicaby a Student: Franziska Peter, Dana G. Berens, Graham R. Grieve and Nina Farwig. 2015. Forest Fragmentation Drives the Loss of Insectivorous Birds and an Associated Increase in Herbivory. Biotropica, 47: 626–635.
My first experience with comprehensive ecological field studies was during my diploma thesis. Under the supervision of Prof. Dr. Tim Diekötter and Dr. Frank Jauker I studied the effects of oilseed rape and semi-natural habitats on pollinator communities and related ecosystem services in a temperate agricultural landscape matrix. Findings were highly complex as pollinator responses were species-specific (with respect to social and nesting behavior as well as morphological traits) and showed temporal and spatial variability. Furthermore, I became aware of the strong and multifaceted consequences of human-driven land-use changes—ranging from the sheer loss of species and shifts in the composition of pollinator communities to cruel things such as ‘nectar robbing’ as well as reduced reproductive success of wild bees and associated wild plants.
Following my diploma thesis, I was excited when Prof. Dr. Nina Farwig welcomed me in her working group. With the PhD position I was given the opportunity to complement my knowledge on effects of human-driven land-use changes on trophic interactions by adding antagonistic plant–herbivore and predator–prey interactions in diverse and structurally complex subtropical forest ecosystems. Being part of a keen research team (supported by the Robert Bosch Stiftung) focusing on the impact of numerous anthropogenic drivers on biotic communities and related ecological processes and ecosystem functioning I could not await the following years. My excitement grew when I first visited South Africa and the previously established study region located at the Oribi Gorge Nature Reserve in southern KwaZulu-Natal. I was astonished by the overwhelming diversity of animal and plant species. Having no experience with subtropical ecosystems it took me a few weeks to be able to identify the majority of tree species within unmanaged rather indigenous forests. However, particularly the fascination about the infinite biodiversity drove me to improve species knowledge, grow expertise for complex trophic interactions in highly diverse forests and fuelled my enthusiasm for fieldwork. As a result, fieldwork, broadening my knowledge in landscape and conservation ecology, daily encounters with wildlife, being integrated in a highly motivated research group as well as the local South African community created an unforgettable experience. A number of South Africans (e.g., Ezemvelo KZN Wildlife, scientists, local farmers) supported and contributed to our work due to their close relationship with nature and their awareness of the value of their highly diverse environment.
I did two subsequent field studies and the nomination of the latter study for Biotropica's Ashton Prize is of great honor to me and my co-authors. The first study focused on main and interactive effects of forest fragmentation and tree diversity on plant–herbivore interactions. In brief, findings of this study revealed that effects of local tree diversity on plant–herbivore interactions diminished with increasing forest fragmentation on the landscape scale. With the second study I aimed to build on previous research that investigated effects of habitat fragmentation on either plant–herbivore or predator–prey interactions. In particular, I was curious whether forest fragmentation triggers cascades across multitrophic interactions and changes patterns in ecosystem functioning. Hence, I simultaneously monitored bird communities, insect herbivore abundances as well as leaf area loss along an increasing degree of forest fragmentation. I quantified the trophic control of herbivorous insects by insectivorous birds through bird exclosures attached to the common tree species Englerophytum natalensis. Installing the bird exclosure and the control at the same plant individual enabled me to exclude confounding effects of the microhabitat and the individual plant history and thus, to focus on the impact of forest fragmentation on plant–herbivore interactions through changes in the local bird community. Findings offered insights into complex effects of forest fragmentation on multitrophic interactions. Both forest fragmentation and vegetation heterogeneity structured the functional composition of bird communities as a result of species-specific forest-dependency and resource requirements as well as preferences for structural forest habitat features. As a consequence, open-habitat omnivorous birds seemed to benefit from forest fragmentation while abundances of forest-dependent insectivorous birds decreased with increasing forest fragmentation. However, I found no significant difference in the abundance of herbivorous insects within the bird exclosure relative to the control which may be explained by the restriction to a rather seasonal ‘snapshot’ of the insect herbivore community. In fact, leaf area loss which accumulated during the study period was higher when birds were excluded supporting the functional role of insectivorous birds for the natural control of herbivorous insects. Finally, the increase in leaf area loss for the control branches with increasing forest fragmentation implies that increasing forest fragmentation diminished the natural control of herbivorous insects by insectivorous birds.
Overall, findings of my study show that forest fragmentation in fact seems to trigger cascades across multitrophic interactions and ultimately, may hamper ecosystem functioning. Therefore, the application of multitrophic approaches offers new insights into the comprehensive impact of anthropogenic drivers and enables to discover changes in ecological processes and thus, ecosystem functioning. In addition, results support previous studies that concluded that the protection and connectivity of preferably large forest habitats benefits ecosystem functioning.
2016年Julie S Denslow和Peter Ashton在Biotropica上发表的杰出文章奖
这个模型现在被扩展到包括更现实的气候动态,以及世界各地的景观和环境。目标是评估全球生物多样性模式在不需要诉诸生物相互作用的情况下被解释的程度——例如,驱动多样性模式的历史与当前生态因素的平衡是什么?这些问题的答案必须等待大量额外的探索和测试,但积极的是,目前正在探索以适当的时空尺度和范围回答这些问题的框架。美国佐治亚州亚特兰大市疾病控制与预防中心疾病生态学家Yoshinori Nakazawa a . Townsend Peterson大学生物多样性研究所及生态与进化生物系特聘教授,美国堪萨斯州劳伦斯市堪萨斯大学Peter Ashton学生杰出论文奖:Franziska Peter, Dana G. Berens, Graham R. Grieve和Nina Farwig, 2015。森林破碎化导致食虫鸟类的减少和草食性鸟类的增加。热带生物学报,47(4):626-635。我第一次接触全面的生态实地研究是在我的毕业论文期间。在Tim博士Diekötter教授和Frank Jauker博士的指导下,我研究了油菜和半自然生境对温带农业景观基质中传粉昆虫群落和相关生态系统服务的影响。研究结果非常复杂,因为传粉者的反应是物种特异性的(在社会和筑巢行为以及形态特征方面),并表现出时空变异性。此外,我开始意识到人类驱动的土地利用变化所带来的强大而多方面的后果——从物种的彻底消失和传粉者群落组成的变化,到“掠夺花蜜”以及野生蜜蜂和相关野生植物繁殖成功率降低等残酷的事情。完成毕业论文后,我很兴奋地看到Dr. Nina Farwig教授邀请我加入她的工作小组。获得博士学位后,我有机会补充我在人类驱动的土地利用变化对营养相互作用的影响方面的知识,在多样化和结构复杂的亚热带森林生态系统中加入拮抗植物-食草动物和捕食者-猎物相互作用。作为一个敏锐的研究团队的一员(由罗伯特·博世基金会支持),专注于众多人为驱动因素对生物群落和相关生态过程和生态系统功能的影响,我迫不及待地期待着接下来的几年。当我第一次访问南非和之前建立的位于夸祖鲁-纳塔尔省南部奥里比峡谷自然保护区的研究区域时,我的兴奋之情越来越强烈。动植物种类的巨大多样性使我感到惊讶。由于没有亚热带生态系统的经验,我花了几个星期的时间才能够在未管理的原始森林中识别出大多数树种。然而,尤其是对无限的生物多样性的迷恋,促使我提高物种知识,培养在高度多样化的森林中复杂的营养相互作用的专业知识,并激发了我对野外工作的热情。因此,实地考察,拓宽了我在景观和保护生态学方面的知识,与野生动物的日常接触,融入一个高度积极的研究小组以及当地的南非社区,创造了一次难忘的经历。许多南非人(如zemvelo KZN野生动物,科学家,当地农民)支持并为我们的工作做出了贡献,因为他们与自然的密切关系以及他们对高度多样化环境价值的认识。我随后进行了两次实地研究,后一项研究被提名为Biotropica的阿什顿奖,这对我和我的合著者来说是极大的荣誉。第一个研究重点是森林破碎化和树木多样性对植物-草食动物相互作用的主要作用和交互作用。总之,本研究结果表明,在景观尺度上,随着森林破碎化程度的增加,当地树木多样性对植物-草食相互作用的影响减弱。在第二项研究中,我的目标是建立在先前研究的基础上,研究栖息地破碎化对植物-食草动物或捕食者-猎物相互作用的影响。我特别好奇的是,森林破碎化是否会引发跨多营养相互作用的级联反应,并改变生态系统功能的模式。因此,我同时监测了鸟类群落、食草昆虫丰度以及随着森林破碎化程度的增加而出现的叶面积损失。通过对常见树种纳塔勒姆(Englerophytum natalensis)上的鸟类进行暴露,量化了食虫鸟类对草食性昆虫的营养控制。
期刊介绍:
Ranked by the ISI index, Biotropica is a highly regarded source of original research on the ecology, conservation and management of all tropical ecosystems, and on the evolution, behavior, and population biology of tropical organisms. Published on behalf of the Association of Tropical Biology and Conservation, the journal''s Special Issues and Special Sections quickly become indispensable references for researchers in the field. Biotropica publishes timely Papers, Reviews, Commentaries, and Insights. Commentaries generate thought-provoking ideas that frequently initiate fruitful debate and discussion, while Reviews provide authoritative and analytical overviews of topics of current conservation or ecological importance. The newly instituted category Insights replaces Short Communications.