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Will a large complex model ecosystem be viable? The essential role of positive interactions
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-19 DOI: 10.1002/ecy.70064
Rudolf P. Rohr, Louis-Félix Bersier, Roger Arditi

Ecologists have documented many characteristics of natural systems that foster ecosystem persistence, and it might be deduced that such strategies are essential for counteracting the negative effect of complexity on local stability that was suggested by R.M. May in his influential work of the 1970s. However, we show that the loss of local stability does not necessarily imply total ecosystem extinction. A more general criterion of ecosystem viability is the long-term persistence of any number of surviving species—not necessarily all of them. With this approach, we show that persistence increases with complexity, contrary to previous theoretical findings. In particular, positive interactions (mutualistic or prey-to-predator) play a crucial role in creating ecological niches, which sustain biodiversity with increasing complexity.

生态学家已经记录了自然系统中许多促进生态系统持久性的特征,由此可以推断,这些策略对于抵消复杂性对局部稳定性的负面影响至关重要。然而,我们的研究表明,局部稳定性的丧失并不一定意味着生态系统的彻底消亡。生态系统生存能力的一个更普遍的标准是任何数量的幸存物种--不一定是所有物种--的长期存在。通过这种方法,我们发现持久性会随着复杂性的增加而增加,这与之前的理论发现相反。特别是,积极的相互作用(互惠或猎物对猎物)在创造生态位方面发挥着至关重要的作用,而生态位会随着复杂性的增加而维持生物多样性。
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引用次数: 0
Bird diversity in historical paintings of the Song dynasty (960–1279)
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-19 DOI: 10.1002/ecy.70070
Qianyu Chen, Shuihua Chen, Shilu Zheng, Rachakonda Sreekar, Zhijun Ma, Jiajia Liu
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引用次数: 0
Tree diversity shapes the spectral signature of light transmittance in developing forests
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-19 DOI: 10.1002/ecy.70032
Laura J. Williams, Kyle R. Kovach, J. Antonio Guzmán Q., Artur Stefanski, Raimundo Bermudez, Ethan E. Butler, Domitille Coq--Etchegaray, Catherine Glenn-Stone, Peter Hajek, Johanna Klama, Belinda E. Medlyn, Christian Messier, Aboubakr Moradi, Alain Paquette, Maria H. Park, Michael Scherer-Lorenzen, Philip A. Townsend, Peter B. Reich, Jeannine Cavender-Bares, Meredith C. Schuman

Greater tree diversity often increases forest productivity by increasing the fraction of light captured and the effectiveness of light use at the community scale. However, light may shape forest function not only as a source of energy or a cause of stress but also as a context cue: Plant photoreceptors can detect specific wavelengths of light, and plants use this information to assess their neighborhoods and adjust their patterns of growth and allocation. These cues have been well documented in laboratory studies, but little studied in diverse forests. Here, we examined how the spectral profile of light (350–2200 nm) transmitted through canopies differs among tree communities within three diversity experiments on two continents (200 plots each planted with one to 12 tree species, amounting to roughly 10,000 trees in total), laying the groundwork for expectations about how diversity in forests may shape light quality with consequences for forest function. We hypothesized—and found—that the species composition and diversity of tree canopies influenced transmittance in predictable ways. Canopy transmittance—in total and in spectral regions with known biological importance—principally declined with increasing leaf area per ground area (LAI) and, in turn, LAI was influenced by the species composition and diversity of communities. For a given LAI, broadleaved angiosperm canopies tended to transmit less light with lower red-to-far-red ratios than canopies of needle-leaved gymnosperms or angiosperm-gymnosperm mixtures. Variation among communities in the transmittance of individual leaves had a minor effect on canopy transmittance in the visible portion of the spectrum but contributed beyond this range along with differences in foliage arrangement. Transmittance through mixed species canopies often deviated from expectations based on monocultures, and this was only partly explained by diversity effects on LAI, suggesting that diversity effects on transmittance also arose through shifts in the arrangement and optical properties of foliage. We posit that differences in the spectral profile of light transmitted through diverse canopies serve as a pathway by which tree diversity affects some forest ecosystem functions.

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引用次数: 0
Imaging spectroscopy reveals topographic variability effects on grassland functional traits and drought responses
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-18 DOI: 10.1002/ecy.70006
Phuong D. Dao, Yuhong He, Bing Lu, Alexander Axiotis

Functional traits and their variations are essential indicators of plant metabolism, growth, distribution, and survival and determine how a plant and an ecosystem function. Under the same climatic condition, traits can vary significantly between species and within the same species growing in different topographic conditions. When drought stress occurs, plants growing in these conditions may respond in various ways as their tolerance and adaptability are influenced by differences in topography. Insights into topographic variability-driven trait variation and drought response can improve our prediction of ecosystem functioning and ecological impacts. Imaging spectroscopy enables accurate identification of plant species, extraction of functional traits, and characterization of topography-driven and drought-related impacts on trait variation across spatial scales. However, applying these data in a heterogeneous grassland ecosystem is challenging as species are small, highly mixed, spectrally and texturally similar, and highly varied with small-scale variation in topography. This paper presents the first study to explore the use of high-resolution airborne imaging spectroscopy for characterizing the variation of key traits—such as chlorophylls (Chl), carotenoids (Car), Chl/Car ratio, water content (WC), and leaf area index (LAI)—across topographic gradients and under drought stress at the species level in a heterogeneous grassland. The results demonstrate significant relationships between functional traits and topographic variability, with the strength of these relationships varying among species and across different environmental conditions. Additionally, drought-induced trait responses differed notably both within and between species, particularly between drought-tolerant invasive species and drought-sensitive native species, as well as between lower and upper slope positions. The study makes a significant contribution to advancing our understanding of biological and ecological processes, enhancing the ability to predict plant invasion mechanism and ecosystem functioning under stressed environments.

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引用次数: 0
GLOSSAQUA: A global dataset of size spectra across aquatic ecosystems
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-18 DOI: 10.1002/ecy.70050
Zeynep Ersoy, Charlotte Evangelista, Aitor Larrañaga, Daniel M. Perkins, Javier Sánchez-Hernández, Teofana Chonova, David Cunillera-Montcusí, Carmen García-Comas, Jorge García-Girón, Ioar de Guzman, Justin Pomeranz, Victor Saito, Matías Arim, Dirceu Baumgartner, Gilmar Baumgartner, Mauro Berazategui, Dani Boix, Giovanna Collyer, Jordi Compte, Almir Manoel Cunico, Renee M. van Dorst, Jon Harding, Ursula Gaedke, Stéphanie Gascón, Éder André Gubiani, Daniel Hernández, James R. Junker, Mercedes López-Vázquez, Anderson Luís Maciel, Thomas Mehner, Roger Paulo Mormul, Ramiro Pereira-Garbero, Danielle Petsch, Pitágoras Augusto Piana, Xavier D. Quintana, Julia Reiss, Lucía Rodríguez-Tricot, Jordi Sala, Wilson Sebastián Serra, Tadeu Siqueira, Helen J. Warburton, Matías Zarucki, Ignasi Arranz

Body size is a key trait in ecology due to its influence on metabolism and many other life-history traits that affect population and community responses to environmental variation as well as ecosystem properties. The size spectrum represents the relationship between abundance (or biomass) and body size, independent of species identity. Size spectrum parameters, such as the slope or intercept, have been applied extensively as indicators of ecological status across multiple ecosystem types. The GLOSSAQUA dataset includes data from mainly heterotrophic communities composed of single (e.g., zooplankton, macroinvertebrates, or fish) to multiple taxonomic groups (e.g., from primary consumers to apex predators, and phytoplankton to large zooplankton), across diverse spatial and temporal scales, from surveys in freshwater (43% studies), marine (52% studies) and brackish (5% studies) ecosystems. In total, we compiled a unique global dataset of 8459 size spectrum slopes or exponents, 5237 intercepts, and 4,497 linearity coefficients (i.e., defined by the R2 of the linear fit of the size spectrum) from 127 articles and gray literature (i.e., unpublished datasets). The current dataset aims to help identify the main drivers shaping aquatic size spectrum parameters at a global scale and contribute to cross-ecosystem comparisons. GLOSSAQUA can serve to explore questions such as factors influencing spatial and temporal dynamics of community size structure, comparing the response of community size structure between natural versus human-impacted sites, and comparing global patterns in different aquatic ecosystems. We encourage researchers, especially those from underrepresented geographical areas (e.g., South Hemisphere and Asia) to fuel this dataset in the future. The dataset is provided under a CC-BY-NC-S4 4.0 license, and users are encouraged to cite this data paper when using the data.

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引用次数: 0
Phenological sensitivity of Bromus tectorum genotypes depends on current and source environments
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-17 DOI: 10.1002/ecy.70025
Megan L. Vahsen, Toby M. Maxwell, Dana M. Blumenthal, Diana Gamba, Matthew J. Germino, Mevin B. Hooten, Jesse R. Lasky, Elizabeth A. Leger, Nikki Pirtel, Lauren M. Porensky, Seth Romero, Justin J. Van Ee, Stella M. Copeland, David J. Ensing, Peter B. Adler

Plants respond to their environment with both short-term, within-generation trait plasticity, and long-term, between-generation evolutionary changes. However, the relative magnitude of plant responses to short- and long-term changes in the environment remains poorly understood. Shifts in phenological traits can serve as harbingers for responses to environmental change, and both a plant's current and source (i.e., genotype origin) environment can affect plant phenology via plasticity and local adaptation, respectively. To assess the role of current and source environments in explaining variation in flowering phenology of Bromus tectorum, an invasive annual grass, we conducted a replicated common garden experiment using 92 genotypes collected across western North America. Replicates of each genotype were planted in two densities (low = 100 seeds/1 m2, high = 100 seeds/0.04 m2) under two different temperature treatments (low = white gravel; high = black gravel; 2.1°C average difference) in a factorial design, replicated across four common garden locations in Idaho and Wyoming, USA. We tested for the effect of current environment (i.e., density treatment, temperature treatment, and common garden location), source environment (i.e., genotype source climate), and their interaction on each plant's flowering phenology. Flowering timing was strongly influenced by a plant's current environment, with plants that experienced warmer current climates and higher densities flowering earlier than those that experienced cooler current climates and lower densities. Genotypes from hot and dry source climates flowered consistently earlier than those from cool and wet source climates, even after accounting for genotype relatedness, suggesting that this genetically based climate cline is a product of natural selection. We found minimal evidence of interactions between current and source environments or genotype-by-environment interactions. Phenology was more sensitive to variation in the current climate than to variation in source climate. These results indicate that cheatgrass phenology reflects high levels of plasticity as well as rapid local adaptation. Both processes likely contribute to its current success as a biological invader and its capacity to respond to future environmental change.

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引用次数: 0
Seasonal structural stability promoted by forest diversity and composition explains overyielding 森林多样性和组成所促进的季节性结构稳定性解释了高产的原因
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-17 DOI: 10.1002/ecy.70055
J. Antonio Guzmán Q., Maria H. Park, Laura J. Williams, Jeannine Cavender-Bares

The stability of forest productivity is a widely studied phenomenon often associated with tree species diversity. Yet, drivers of stability in forest structure and its consequences for forest productivity remain poorly understood. Using a large (10 ha) young tree diversity experiment, we evaluated how forest structure and multiple dimensions of diversity and composition are related to remotely sensed structural metrics and their stability through the growing season. We then examined whether structural stability (SS) across the growing season (April–October) could explain overyielding (i.e., the net biodiversity effect, NBE) in annual wood productivity. Using Uncrewed Aerial Vehicle-Light Detecting and Ranging (UAV-LiDAR), we surveyed experimental tree communities eight times at regular intervals from before bud break to after leaf senescence to derive metrics associated with canopy height heterogeneity, fractional plant cover, and forest structural complexity (based on fractal geometry). The inverse coefficients of variation for each of these three metrics through the season were used as measures of SS. These metrics were then coupled with annual tree inventories to evaluate their relationships with the NBE. Our findings indicate that wood volume and, to some extent, multiple dimensions of diversity and composition (i.e., taxonomic, phylogenetic, and functional) explain remotely sensed metrics of forest structure and their SS. Increases in wood volume as well as functional and phylogenetic diversity and variability (a measure of diversity independent of species richness) were linked to higher SS of forest complexity and canopy height heterogeneity. We further found that higher SS of forest complexity and fractional plant cover were associated with increased overyielding, which was mostly attributable to the complementarity effect. Structural equation models indicate that the stability of structural complexity explains more variation in NBE among plots than dimensions of diversity or variability, highlighting its value as an informative metric that likely integrates multiple drivers associated with overyielding. This study highlights the potential to integrate remote sensing and ecology to disentangle the role of forest SS in shaping ecological processes.

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引用次数: 0
Potential caterpillar mimicry in a tropical hummingbird
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-17 DOI: 10.1002/ecy.70060
Jay J. Falk, Michael Castaño-Diaz, Sebastian Gallan-Giraldo, Joseph See, Scott Taylor
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引用次数: 0
Blue angels have devil hands: Predatory behavior using cerata in Glaucus atlanticus
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-17 DOI: 10.1002/ecy.70062
Gaku Yamamoto, Naoki Kanai, Toru Miura, Kohei Oguchi
<p>Nudibranchs, a subset of gastropods within the phylum Mollusca, encompass over 3000 valid species worldwide, characterized by the thinning or internalization of a shell (Do et al., <span>2022</span>; Goodheart et al., <span>2015</span>; Valdés, <span>2004</span>). In place of shells, nudibranchs have evolved various alternative defense tactics, including vibrant warning or camouflage coloration (Paul & Ritson-Williams, <span>2008</span>; Wägele & Klussmann-Kolb, <span>2005</span>). Among nudibranch species belonging to Cladobranchia, most employ nematocysts stolen from dietary benthic cnidarians such as hydrozoans and anemones for defense, as known as “kleptocnidae.” These nematocysts are incorporated inside dorsal projections called “cerata (singular: ceras)” (Edmunds, <span>1966</span>; Goodheart et al., <span>2017</span>, <span>2018</span>; Greenwood, <span>2009</span>; Grosvenor, <span>1903</span>; Kepner, <span>1943</span>; Putz et al., <span>2010</span>). Nematocysts are a type of organelle unique to cnidarians; these pouch-like structures invert in response to mechanical and/or chemical stimuli, to release toxic needles (Holstein & Tardent, <span>1984</span>). Remarkably, cladobranchs can capture and store nematocysts in the distal part of each ceras in an organ called the “cnidosac,” which are expelled when attacked by predators (Goodheart et al., <span>2017</span>, <span>2018</span>; Greenwood, <span>2009</span>; Grosvenor, <span>1903</span>). During the process of incorporating the ingested nematocysts, they are transported through the digestive tract into specialized cells called “cnidophages” located in the cnidosac (Goodheart et al., <span>2017</span>, <span>2018</span>; Greenwood, <span>2009</span>; Grosvenor, <span>1903</span>).</p><p>Unlike most cladobranchs, which have cerata on their dorsal sides, all species of the genus <i>Glaucus</i> (the sole genus in the family Glaucidae), bear several paired fin-like projections on each side of their bodies (Thompson & Bennett, <span>1970</span>; Thompson & McFarlane, <span>1967</span>). <i>Glaucus</i> species live by floating with air inside their bodies and their ventral side facing the surface of the water (Thompson & McFarlane, <span>1967</span>). Due to their distinctive body plan and their silvery-white dorsal and blue ventral coloration, they are often called “blue angels,” “blue dragons” or “sea swallows” (Figure 1a). Unlike many other nudibranchs which are benthic, all species of <i>Glaucus</i> are pleuston (sometimes termed neuston) species that live on the ocean's surface, using cerata and air bubbles in their stomach cavities for buoyancy (Miller, <span>1974</span>; Thompson & Bennett, <span>1970</span>; Thompson & McFarlane, <span>1967</span>). They are carnivorous and prey on other pleustonic cnidarian species, including bluebottles (<i>Physalia</i> sp.), sea rafts (<i>Velella velella</i>), and blue buttons (<i>Porpita porpita</i>) (Bieri, <
{"title":"Blue angels have devil hands: Predatory behavior using cerata in Glaucus atlanticus","authors":"Gaku Yamamoto,&nbsp;Naoki Kanai,&nbsp;Toru Miura,&nbsp;Kohei Oguchi","doi":"10.1002/ecy.70062","DOIUrl":"https://doi.org/10.1002/ecy.70062","url":null,"abstract":"&lt;p&gt;Nudibranchs, a subset of gastropods within the phylum Mollusca, encompass over 3000 valid species worldwide, characterized by the thinning or internalization of a shell (Do et al., &lt;span&gt;2022&lt;/span&gt;; Goodheart et al., &lt;span&gt;2015&lt;/span&gt;; Valdés, &lt;span&gt;2004&lt;/span&gt;). In place of shells, nudibranchs have evolved various alternative defense tactics, including vibrant warning or camouflage coloration (Paul &amp; Ritson-Williams, &lt;span&gt;2008&lt;/span&gt;; Wägele &amp; Klussmann-Kolb, &lt;span&gt;2005&lt;/span&gt;). Among nudibranch species belonging to Cladobranchia, most employ nematocysts stolen from dietary benthic cnidarians such as hydrozoans and anemones for defense, as known as “kleptocnidae.” These nematocysts are incorporated inside dorsal projections called “cerata (singular: ceras)” (Edmunds, &lt;span&gt;1966&lt;/span&gt;; Goodheart et al., &lt;span&gt;2017&lt;/span&gt;, &lt;span&gt;2018&lt;/span&gt;; Greenwood, &lt;span&gt;2009&lt;/span&gt;; Grosvenor, &lt;span&gt;1903&lt;/span&gt;; Kepner, &lt;span&gt;1943&lt;/span&gt;; Putz et al., &lt;span&gt;2010&lt;/span&gt;). Nematocysts are a type of organelle unique to cnidarians; these pouch-like structures invert in response to mechanical and/or chemical stimuli, to release toxic needles (Holstein &amp; Tardent, &lt;span&gt;1984&lt;/span&gt;). Remarkably, cladobranchs can capture and store nematocysts in the distal part of each ceras in an organ called the “cnidosac,” which are expelled when attacked by predators (Goodheart et al., &lt;span&gt;2017&lt;/span&gt;, &lt;span&gt;2018&lt;/span&gt;; Greenwood, &lt;span&gt;2009&lt;/span&gt;; Grosvenor, &lt;span&gt;1903&lt;/span&gt;). During the process of incorporating the ingested nematocysts, they are transported through the digestive tract into specialized cells called “cnidophages” located in the cnidosac (Goodheart et al., &lt;span&gt;2017&lt;/span&gt;, &lt;span&gt;2018&lt;/span&gt;; Greenwood, &lt;span&gt;2009&lt;/span&gt;; Grosvenor, &lt;span&gt;1903&lt;/span&gt;).&lt;/p&gt;&lt;p&gt;Unlike most cladobranchs, which have cerata on their dorsal sides, all species of the genus &lt;i&gt;Glaucus&lt;/i&gt; (the sole genus in the family Glaucidae), bear several paired fin-like projections on each side of their bodies (Thompson &amp; Bennett, &lt;span&gt;1970&lt;/span&gt;; Thompson &amp; McFarlane, &lt;span&gt;1967&lt;/span&gt;). &lt;i&gt;Glaucus&lt;/i&gt; species live by floating with air inside their bodies and their ventral side facing the surface of the water (Thompson &amp; McFarlane, &lt;span&gt;1967&lt;/span&gt;). Due to their distinctive body plan and their silvery-white dorsal and blue ventral coloration, they are often called “blue angels,” “blue dragons” or “sea swallows” (Figure 1a). Unlike many other nudibranchs which are benthic, all species of &lt;i&gt;Glaucus&lt;/i&gt; are pleuston (sometimes termed neuston) species that live on the ocean's surface, using cerata and air bubbles in their stomach cavities for buoyancy (Miller, &lt;span&gt;1974&lt;/span&gt;; Thompson &amp; Bennett, &lt;span&gt;1970&lt;/span&gt;; Thompson &amp; McFarlane, &lt;span&gt;1967&lt;/span&gt;). They are carnivorous and prey on other pleustonic cnidarian species, including bluebottles (&lt;i&gt;Physalia&lt;/i&gt; sp.), sea rafts (&lt;i&gt;Velella velella&lt;/i&gt;), and blue buttons (&lt;i&gt;Porpita porpita&lt;/i&gt;) (Bieri, &lt;","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 3","pages":""},"PeriodicalIF":4.4,"publicationDate":"2025-03-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.70062","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143632909","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Altitude sickness in pollinators: Skyward emigration holds consequences for a native bee
IF 4.4 2区 环境科学与生态学 Q1 ECOLOGY Pub Date : 2025-03-12 DOI: 10.1002/ecy.70063
Shawn A. Steffan, Prarthana S. Dharampal
<p>In the era of climate change, organisms globally are being challenged to adapt to increasingly extreme stressors (Lloret et al., <span>2012</span>; Walters et al., <span>2012</span>). Such climate stressors are often typified by heat spikes, severe drought, flooding, and fire (Wagner, <span>2020</span>). For animals requiring snow cover (i.e., the space between snow and soil, also known as the <i>subnivium</i>) to survive winter, this refuge space has been retreating skyward (higher in altitude) and poleward (higher in latitude) as climates warm (Pauli et al., <span>2013</span>). With the increasing severity of climate stressors, the elevational ranges of plant species are pushing skyward (Jump et al., <span>2009</span>; Kelly & Goulden, <span>2008</span>), as are many insect populations (Hodkinson, <span>2005</span>). Indeed, an emerging biogeographic pattern associated with climate change is the skyward and poleward redistribution of plant and animal populations (Hodkinson, <span>2005</span>; Jump et al., <span>2009</span>). Among pollinator communities, climate change has been linked to continental-scale redistributions of bee taxa (Ghisbain et al., <span>2023</span>), reductions in bee size over the last three decades (Herrera et al., <span>2023</span>), and precipitous declines in general abundance (Wagner, <span>2020</span>). The channeling and redistribution of species are expected to increase in frequency and magnitude globally (Hodkinson, <span>2005</span>; Jump et al., <span>2009</span>).</p><p>High-elevation habitats may serve as near-term biodiversity reservoirs (“sky islands”), particularly for pollinator communities (Wagner, <span>2020</span>), as climate stressors reduce the viability of populations at lower elevations (Kelly & Goulden, <span>2008</span>; Lloret et al., <span>2012</span>). Pollinators and other organisms seeking refuge from excessive heat may find skyward dispersal more expedient than poleward dispersal, given that a 1°C decline in temperature can be achieved (on average) with a 167-m increase in altitude, while the same drop in temperature would necessitate a 145 km increase in latitude (Jump et al., <span>2009</span>). However, any elevational gradient will be associated with decreasing air pressure (Peacock, <span>1998</span>), which will impose a degree of hypoxia on colonizing organisms (Hoback & Stanley, <span>2001</span>; Hodkinson, <span>2005</span>). Insect species developing under depleted oxygen (O<sub>2</sub>) concentrations in controlled laboratory conditions are known to exhibit smaller adult sizes, reduced reproductive capacity, and lower survival rates (Harrison et al., <span>2018</span>), all of which represent major fitness consequences for insects (Honěk, <span>1993</span>; Kingsolver & Huey, <span>2008</span>). This begs the question as to whether altitudinal hypoxia might produce the same types of consequences as artificially reduced O<sub>2</sub> in laboratory experiments.</
{"title":"Altitude sickness in pollinators: Skyward emigration holds consequences for a native bee","authors":"Shawn A. Steffan,&nbsp;Prarthana S. Dharampal","doi":"10.1002/ecy.70063","DOIUrl":"https://doi.org/10.1002/ecy.70063","url":null,"abstract":"&lt;p&gt;In the era of climate change, organisms globally are being challenged to adapt to increasingly extreme stressors (Lloret et al., &lt;span&gt;2012&lt;/span&gt;; Walters et al., &lt;span&gt;2012&lt;/span&gt;). Such climate stressors are often typified by heat spikes, severe drought, flooding, and fire (Wagner, &lt;span&gt;2020&lt;/span&gt;). For animals requiring snow cover (i.e., the space between snow and soil, also known as the &lt;i&gt;subnivium&lt;/i&gt;) to survive winter, this refuge space has been retreating skyward (higher in altitude) and poleward (higher in latitude) as climates warm (Pauli et al., &lt;span&gt;2013&lt;/span&gt;). With the increasing severity of climate stressors, the elevational ranges of plant species are pushing skyward (Jump et al., &lt;span&gt;2009&lt;/span&gt;; Kelly &amp; Goulden, &lt;span&gt;2008&lt;/span&gt;), as are many insect populations (Hodkinson, &lt;span&gt;2005&lt;/span&gt;). Indeed, an emerging biogeographic pattern associated with climate change is the skyward and poleward redistribution of plant and animal populations (Hodkinson, &lt;span&gt;2005&lt;/span&gt;; Jump et al., &lt;span&gt;2009&lt;/span&gt;). Among pollinator communities, climate change has been linked to continental-scale redistributions of bee taxa (Ghisbain et al., &lt;span&gt;2023&lt;/span&gt;), reductions in bee size over the last three decades (Herrera et al., &lt;span&gt;2023&lt;/span&gt;), and precipitous declines in general abundance (Wagner, &lt;span&gt;2020&lt;/span&gt;). The channeling and redistribution of species are expected to increase in frequency and magnitude globally (Hodkinson, &lt;span&gt;2005&lt;/span&gt;; Jump et al., &lt;span&gt;2009&lt;/span&gt;).&lt;/p&gt;&lt;p&gt;High-elevation habitats may serve as near-term biodiversity reservoirs (“sky islands”), particularly for pollinator communities (Wagner, &lt;span&gt;2020&lt;/span&gt;), as climate stressors reduce the viability of populations at lower elevations (Kelly &amp; Goulden, &lt;span&gt;2008&lt;/span&gt;; Lloret et al., &lt;span&gt;2012&lt;/span&gt;). Pollinators and other organisms seeking refuge from excessive heat may find skyward dispersal more expedient than poleward dispersal, given that a 1°C decline in temperature can be achieved (on average) with a 167-m increase in altitude, while the same drop in temperature would necessitate a 145 km increase in latitude (Jump et al., &lt;span&gt;2009&lt;/span&gt;). However, any elevational gradient will be associated with decreasing air pressure (Peacock, &lt;span&gt;1998&lt;/span&gt;), which will impose a degree of hypoxia on colonizing organisms (Hoback &amp; Stanley, &lt;span&gt;2001&lt;/span&gt;; Hodkinson, &lt;span&gt;2005&lt;/span&gt;). Insect species developing under depleted oxygen (O&lt;sub&gt;2&lt;/sub&gt;) concentrations in controlled laboratory conditions are known to exhibit smaller adult sizes, reduced reproductive capacity, and lower survival rates (Harrison et al., &lt;span&gt;2018&lt;/span&gt;), all of which represent major fitness consequences for insects (Honěk, &lt;span&gt;1993&lt;/span&gt;; Kingsolver &amp; Huey, &lt;span&gt;2008&lt;/span&gt;). This begs the question as to whether altitudinal hypoxia might produce the same types of consequences as artificially reduced O&lt;sub&gt;2&lt;/sub&gt; in laboratory experiments.&lt;/","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 3","pages":""},"PeriodicalIF":4.4,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.70063","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143602512","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Ecology
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