Victoria J. Luizzi, A. Elizabeth Arnold, Judith L. Bronstein
Many insects damage leaves, a phenomenon that is foundational to their impacts on terrestrial ecosystems. Leaf traits, including chemistry, shape these interactions. In turn, leaf-surface (phylloplane) microbes can act directly or in concert with leaf chemistry to influence leaf choice, especially by insects whose reproductive success is tied to prolonged contact with leaf surfaces. Leafcutter bees (Megachile spp.) cut disks from leaves to line their nests, with leaves and their associated microbes forming the environment in which bees' offspring develop. We hypothesized that phylloplane microbial communities act in concert with leaf chemistry to mediate interactions between the leafcutter bee M. lippiae and the plants they cut. We surveyed phylloplane communities on rose (Rosa × hybrida, Rosaceae) leaflets that were cut versus not cut by wild M. lippiae. Microbial communities differed between cut and non-cut leaflets, with Aspergillus spp. overrepresented on cut leaflets, and Alternaria sp. and Bacillus sp. overrepresented on non-cut leaflets. Then, we inoculated rose leaves in the field to test the effect of these microbial taxa on cutting. When inoculated onto rose leaves, Alternaria and Bacillus had no effect on cutting, but Aspergillus resulted in twice as many cuts as on sham-inoculated leaves. To test whether Aspergillus could protect bee nests against pathogens, we grew Aspergillus with two pathogenic fungi: the generalist insect pathogen Beauveria bassiania and three strains of Ascosphaera that cause chalkbrood disease in bee larvae. Aspergillus did not inhibit the growth of Beauveria, but it markedly slowed the growth of Ascosphaera. To clarify whether these phylloplane microbes reflect differences in leaf chemistry or are instead independent cues that influence leaf cutting, we used liquid chromatography-mass spectroscopy to characterize the metabolome of cut and non-cut leaflets. Chemistry did not differ between cut and non-cut leaflets, nor did it vary as a function of microbial community composition. Our results suggest that Aspergillus, a common member of rose phylloplane communities, mediates interactions between leafcutter bees and roses, potentially affecting the fitness of both partners. This study reveals a previously unexplored role for phylloplane microbes in plant–insect associations.
{"title":"A leaf-surface fungus mediates interactions between leafcutter bees and the plants they cut to line their nests","authors":"Victoria J. Luizzi, A. Elizabeth Arnold, Judith L. Bronstein","doi":"10.1002/ecy.70229","DOIUrl":"https://doi.org/10.1002/ecy.70229","url":null,"abstract":"<p>Many insects damage leaves, a phenomenon that is foundational to their impacts on terrestrial ecosystems. Leaf traits, including chemistry, shape these interactions. In turn, leaf-surface (phylloplane) microbes can act directly or in concert with leaf chemistry to influence leaf choice, especially by insects whose reproductive success is tied to prolonged contact with leaf surfaces. Leafcutter bees (<i>Megachile</i> spp.) cut disks from leaves to line their nests, with leaves and their associated microbes forming the environment in which bees' offspring develop. We hypothesized that phylloplane microbial communities act in concert with leaf chemistry to mediate interactions between the leafcutter bee <i>M. lippiae</i> and the plants they cut. We surveyed phylloplane communities on rose (<i>Rosa × hybrida</i>, Rosaceae) leaflets that were cut versus not cut by wild <i>M. lippiae</i>. Microbial communities differed between cut and non-cut leaflets, with <i>Aspergillus</i> spp. overrepresented on cut leaflets, and <i>Alternaria</i> sp. and <i>Bacillus</i> sp. overrepresented on non-cut leaflets. Then, we inoculated rose leaves in the field to test the effect of these microbial taxa on cutting. When inoculated onto rose leaves, <i>Alternaria</i> and <i>Bacillus</i> had no effect on cutting, but <i>Aspergillus</i> resulted in twice as many cuts as on sham-inoculated leaves. To test whether <i>Aspergillus</i> could protect bee nests against pathogens, we grew <i>Aspergillus</i> with two pathogenic fungi: the generalist insect pathogen <i>Beauveria bassiania</i> and three strains of <i>Ascosphaera</i> that cause chalkbrood disease in bee larvae. <i>Aspergillus</i> did not inhibit the growth of <i>Beauveria</i>, but it markedly slowed the growth of <i>Ascosphaera</i>. To clarify whether these phylloplane microbes reflect differences in leaf chemistry or are instead independent cues that influence leaf cutting, we used liquid chromatography-mass spectroscopy to characterize the metabolome of cut and non-cut leaflets. Chemistry did not differ between cut and non-cut leaflets, nor did it vary as a function of microbial community composition. Our results suggest that <i>Aspergillus</i>, a common member of rose phylloplane communities, mediates interactions between leafcutter bees and roses, potentially affecting the fitness of both partners. This study reveals a previously unexplored role for phylloplane microbes in plant–insect associations.</p>","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145317392","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"High rises and optimal temperatures: Grasshopper microclimate selection","authors":"Nadia Alhassani, Ellen A. R. Welti","doi":"10.1002/ecy.70232","DOIUrl":"https://doi.org/10.1002/ecy.70232","url":null,"abstract":"","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145317680","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Lisa A. Levin, Eulogio Soto, Yerko Castillo, Patricia Esquete, Jeffrey Marlow
<p>Congrio Colorado (<i>Genypterus chilensis</i> (Guichenot, 1848), Ophidiidae), commonly known in English as the red cusk eel, is often found in rocky habitat and coastal waters along the East Pacific margin. It occurs from northern Peru (5°05′ S) to Cape Horn in southern Chile (55°68′ S) (Reyes & Hüne, <span>2012</span>), typically at depths between 2 and 350 m. The species is large, with an average total length of around 60 cm, but attaining lengths around 160 cm (Tascheri et al., <span>2003</span>), and reaching sexual maturity at 72 cm (Chong & González, <span>2009</span>). Congrio Colorado is of commercial significance to artisanal Chilean fishers, with catches greater than 2000 tons by 2022 (Servicio Nacional de Pesca y Acuicultura, <span>2023</span>). It is a menu regular in the seaside restaurants of Chile, and is the subject of a lauded and highly allegorical “Oda al Caldillo de Congrio” [Ode to conger chowder], written by the famous Chilean poet Pablo Neruda (Neruda, <span>1954</span>). Congrio Colorado is considered a demersal-benthic fish not previously associated with chemosynthetic ecosystems.</p><p>A recent oceanographic expedition in October 2024 onboard the RV <i>Falkor (too)</i> explored the methane seeps of Central Chile. Multiple carbonate mounds indicative of methane seepage were identified with the aid of shipboard multibeam, sub-bottom profiling, and M3 mapping on the remotely operated vehicle (ROV). The surveys revealed a series of carbonate mounds topped by large <i>Lamellibrachia</i> sp. tubeworm bushes offshore of El Quisco, south of Valparaiso at a water depth of 434–438 m. These tubeworms are siboglinid polychaetes that obtain nutrition from symbiotic bacteria reliant on methane and hydrogen sulfide released from within the seep (Dubilier et al., <span>2008</span>). They form dense three-dimensional structures that provide habitat for many invertebrates and fishes (Tunnicliffe & Cordes, <span>2021</span>). One of the largest of these tubeworm mounds (37 × 24 m across and approximately 7 m high) was occupied by many <i>G. chilensis</i>, tunneled deep among the tubeworms with only their heads protruding (Figure 1A,B; Videos S1 and S2). <i>G. chilensis</i> were observed to reverse swim into their resting location within the tubeworms (Video S1). Backward swimming in elongated deep-sea fishes, including Ophidiidae, has recently been reported by Priede and Jamieson (<span>2025</span>). Counts of <i>G. chilensis</i> made from video of this mound taken on two separate dives on consecutive days (October 17 and 18, 2024) estimated that 46–48 individual fish were present in the one large mound.</p><p>The Congrio mound was located at 33.3716° S, 71.8931° W, 18 km from the coast, and in a seafloor area with clear signs of fishing activity. Lost fishing nets, floats, and lines were observed frequently during the dives. Surveys of four smaller seep mounds to the west and seven mounds to the north revealed only three Co
奎斯科渗漏点对主要渔业物种的潜在重要性表明,它值得考虑作为海洋保护区。作者声明无利益冲突。
{"title":"Congregation of cusk-eels (Genypterus chilensis, Ophidiiformes) at a deep-sea methane seep off Chile","authors":"Lisa A. Levin, Eulogio Soto, Yerko Castillo, Patricia Esquete, Jeffrey Marlow","doi":"10.1002/ecy.70237","DOIUrl":"10.1002/ecy.70237","url":null,"abstract":"<p>Congrio Colorado (<i>Genypterus chilensis</i> (Guichenot, 1848), Ophidiidae), commonly known in English as the red cusk eel, is often found in rocky habitat and coastal waters along the East Pacific margin. It occurs from northern Peru (5°05′ S) to Cape Horn in southern Chile (55°68′ S) (Reyes & Hüne, <span>2012</span>), typically at depths between 2 and 350 m. The species is large, with an average total length of around 60 cm, but attaining lengths around 160 cm (Tascheri et al., <span>2003</span>), and reaching sexual maturity at 72 cm (Chong & González, <span>2009</span>). Congrio Colorado is of commercial significance to artisanal Chilean fishers, with catches greater than 2000 tons by 2022 (Servicio Nacional de Pesca y Acuicultura, <span>2023</span>). It is a menu regular in the seaside restaurants of Chile, and is the subject of a lauded and highly allegorical “Oda al Caldillo de Congrio” [Ode to conger chowder], written by the famous Chilean poet Pablo Neruda (Neruda, <span>1954</span>). Congrio Colorado is considered a demersal-benthic fish not previously associated with chemosynthetic ecosystems.</p><p>A recent oceanographic expedition in October 2024 onboard the RV <i>Falkor (too)</i> explored the methane seeps of Central Chile. Multiple carbonate mounds indicative of methane seepage were identified with the aid of shipboard multibeam, sub-bottom profiling, and M3 mapping on the remotely operated vehicle (ROV). The surveys revealed a series of carbonate mounds topped by large <i>Lamellibrachia</i> sp. tubeworm bushes offshore of El Quisco, south of Valparaiso at a water depth of 434–438 m. These tubeworms are siboglinid polychaetes that obtain nutrition from symbiotic bacteria reliant on methane and hydrogen sulfide released from within the seep (Dubilier et al., <span>2008</span>). They form dense three-dimensional structures that provide habitat for many invertebrates and fishes (Tunnicliffe & Cordes, <span>2021</span>). One of the largest of these tubeworm mounds (37 × 24 m across and approximately 7 m high) was occupied by many <i>G. chilensis</i>, tunneled deep among the tubeworms with only their heads protruding (Figure 1A,B; Videos S1 and S2). <i>G. chilensis</i> were observed to reverse swim into their resting location within the tubeworms (Video S1). Backward swimming in elongated deep-sea fishes, including Ophidiidae, has recently been reported by Priede and Jamieson (<span>2025</span>). Counts of <i>G. chilensis</i> made from video of this mound taken on two separate dives on consecutive days (October 17 and 18, 2024) estimated that 46–48 individual fish were present in the one large mound.</p><p>The Congrio mound was located at 33.3716° S, 71.8931° W, 18 km from the coast, and in a seafloor area with clear signs of fishing activity. Lost fishing nets, floats, and lines were observed frequently during the dives. Surveys of four smaller seep mounds to the west and seven mounds to the north revealed only three Co","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://esajournals.onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.70237","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145314556","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}
Yolanda M. G. Piñanez Espejo, Ana Munévar, Gustavo A. Zurita, Pablo E. Schilman
Ectotherms with lower maintenance costs and broader environmental tolerances are generally more resilient in human-altered landscapes and under current climate change, enhancing their chances of survival and colonization. In this study, we explored how habitat use and foraging strategy are associated with the resting metabolic rate (RMR) of spiders from habitats with significant temperature variability due to anthropogenic disturbance: native forests and young pine plantations, both in the Southern Atlantic Forest. Using open-flow respirometry at 25°C, we measured CO2 production in immobile spiders to calculate their RMR. Key findings include: (1) all spiders showed 22%–57% lower RMR than predicted by standard metabolic equations; (2) continuous gas exchange patterns, typical of mesic-adapted species, were observed in all cases; (3) the metabolic rate scaling exponent was 0.65; (4) there were no significant RMR differences between habitats, but a negative correlation between RMR and microhabitat thermal amplitude was noted; and (5) active foragers had higher RMRs than passive foragers. These findings enhance our understanding of spider biology, physiology, and ecology, particularly in their responses to anthropogenic stressors.
{"title":"Is spider resting metabolic rate more strongly associated with ecological guild or extreme habitat conditions?","authors":"Yolanda M. G. Piñanez Espejo, Ana Munévar, Gustavo A. Zurita, Pablo E. Schilman","doi":"10.1002/ecy.70231","DOIUrl":"10.1002/ecy.70231","url":null,"abstract":"<p>Ectotherms with lower maintenance costs and broader environmental tolerances are generally more resilient in human-altered landscapes and under current climate change, enhancing their chances of survival and colonization. In this study, we explored how habitat use and foraging strategy are associated with the resting metabolic rate (RMR) of spiders from habitats with significant temperature variability due to anthropogenic disturbance: native forests and young pine plantations, both in the Southern Atlantic Forest. Using open-flow respirometry at 25°C, we measured CO<sub>2</sub> production in immobile spiders to calculate their RMR. Key findings include: (1) all spiders showed 22%–57% lower RMR than predicted by standard metabolic equations; (2) continuous gas exchange patterns, typical of mesic-adapted species, were observed in all cases; (3) the metabolic rate scaling exponent was 0.65; (4) there were no significant RMR differences between habitats, but a negative correlation between RMR and microhabitat thermal amplitude was noted; and (5) active foragers had higher RMRs than passive foragers. These findings enhance our understanding of spider biology, physiology, and ecology, particularly in their responses to anthropogenic stressors.</p>","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://esajournals.onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.70231","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145288951","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}
Jean Carlos Santos, Guilherme Ramos Demetrio, Henrique Venâncio, Fernanda Cristina Franco Cintra, Maria Virginia Urso-Guimarães, Valéria Cid Maia, Walter Santos de Araújo, Pablo Cuevas-Reyes, Wanessa Rejane de Almeida, Guilherme Magalhães Viana
Galls play a significant role in the plant–insect interactions in various ecosystems worldwide. Consequently, research on gall-inducing insects and their host plants has garnered considerable attention in recent years, with a wealth of uncompiled data. This dataset, comprising 2,059 records of 868 native species, 361 genera, and 106 families of host plants, provides valuable information regarding the Atlantic Forest biome, one of the world's most important rainforests. The five most common botanical families represented in the dataset are Myrtaceae, Asteraceae, Fabaceae, Melastomataceae, and Rubiaceae, accounting for 40.41% of all records and 40.21% of the total number of species. In addition, exotic host plant species from families such as Anacardiaceae, Asteraceae, Fabaceae, Myrtaceae, and Verbenaceae are presented. The dataset also includes 204 species of gall-inducing insects, with a large predominance of Diptera (189 species), followed by seven species of Hemiptera, four species of Lepidoptera, and two species each of Coleoptera and Thysanoptera. This study is the first to compile inventories of plant-galling insect communities and information on the diversity and distribution of insect galls and their host plants in the Atlantic Forest. The dataset highlights areas for further research on patterns of diversity and distribution and offers a foundation for developing and testing new ecological hypotheses. Researchers are encouraged to cite this data paper when utilizing the information in their publications and to inform us of the application of the data. No copyright restrictions were applied to the dataset.
{"title":"Plant-herbivore interactions in Atlantic Forest: A dataset of host plants and their gall-inducing insects","authors":"Jean Carlos Santos, Guilherme Ramos Demetrio, Henrique Venâncio, Fernanda Cristina Franco Cintra, Maria Virginia Urso-Guimarães, Valéria Cid Maia, Walter Santos de Araújo, Pablo Cuevas-Reyes, Wanessa Rejane de Almeida, Guilherme Magalhães Viana","doi":"10.1002/ecy.70230","DOIUrl":"10.1002/ecy.70230","url":null,"abstract":"<p>Galls play a significant role in the plant–insect interactions in various ecosystems worldwide. Consequently, research on gall-inducing insects and their host plants has garnered considerable attention in recent years, with a wealth of uncompiled data. This dataset, comprising 2,059 records of 868 native species, 361 genera, and 106 families of host plants, provides valuable information regarding the Atlantic Forest biome, one of the world's most important rainforests. The five most common botanical families represented in the dataset are Myrtaceae, Asteraceae, Fabaceae, Melastomataceae, and Rubiaceae, accounting for 40.41% of all records and 40.21% of the total number of species. In addition, exotic host plant species from families such as Anacardiaceae, Asteraceae, Fabaceae, Myrtaceae, and Verbenaceae are presented. The dataset also includes 204 species of gall-inducing insects, with a large predominance of Diptera (189 species), followed by seven species of Hemiptera, four species of Lepidoptera, and two species each of Coleoptera and Thysanoptera. This study is the first to compile inventories of plant-galling insect communities and information on the diversity and distribution of insect galls and their host plants in the Atlantic Forest. The dataset highlights areas for further research on patterns of diversity and distribution and offers a foundation for developing and testing new ecological hypotheses. Researchers are encouraged to cite this data paper when utilizing the information in their publications and to inform us of the application of the data. No copyright restrictions were applied to the dataset.</p>","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://esajournals.onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.70230","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145288110","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}
Sean M. Johnson-Bice, Frank B. Baldwin, Evan S. Richardson, James D. Roth
Predator use of resource subsidies can strengthen top-down effects on prey when predators respond numerically to subsidies. Although allochthonous subsidies are generally transported along natural gradients, consumers can cross ecosystem boundaries to acquire subsidies, thereby linking disparate ecosystems. In coastal Arctic ecosystems, terrestrial predators like Arctic foxes (Vulpes lagopus) cross into the marine environment (sea ice) during winter to access marine resources. Arctic foxes kill seal pups and scavenge seal carrion (often remains from polar bear Ursus maritimus kills), especially when rodent abundance is low. Terrestrial predator use of marine subsidies may strengthen the top-down control of tundra food webs, but this hypothesis remained untested. We evaluated tundra food web dynamics at the terrestrial–marine interface from an ecosystem-level perspective by assessing: (1) how winter environmental conditions affect rodent abundance and marine subsidy availability, (2) the response of the Arctic fox population to this seasonal food variability, and (3) the subsequent effects of Arctic foxes on Canada goose (Branta canadensis interior) reproduction. Arctic foxes responded numerically to rodent abundance, which was positively related to snow persistence. Arctic fox abundance was positively related to polar bear body condition metrics, which were used as a proxy for marine subsidy availability. Canada goose reproductive success, in turn, was negatively related to Arctic fox abundance. Long-term trends in goose reproduction and snow persistence also indicate an ongoing phenological mismatch between nesting initiation and spring onset. Our results reveal near-term apparent competition between rodents and geese through a shared predator, Arctic foxes, contrasting with prior studies evaluating rodent–goose–predator relationships. Moreover, we establish a link between tundra and sea ice food webs by demonstrating how seal availability can affect goose reproduction indirectly by increasing Arctic fox predation on goose nests via a population response of foxes to marine resources. These marine resources are often provisioned by polar bears, and with both Arctic foxes and polar bears undergoing long-term regional declines evidently driven by climate-related changes in prey abundance and availability, we contextualize our study within ongoing climate change and highlight the vulnerability of this likely widespread terrestrial–marine linkage in a warming Arctic.
{"title":"Marine resources alter tundra food web dynamics by subsidizing a terrestrial predator on the sea ice","authors":"Sean M. Johnson-Bice, Frank B. Baldwin, Evan S. Richardson, James D. Roth","doi":"10.1002/ecy.70204","DOIUrl":"10.1002/ecy.70204","url":null,"abstract":"<p>Predator use of resource subsidies can strengthen top-down effects on prey when predators respond numerically to subsidies. Although allochthonous subsidies are generally transported along natural gradients, consumers can cross ecosystem boundaries to acquire subsidies, thereby linking disparate ecosystems. In coastal Arctic ecosystems, terrestrial predators like Arctic foxes (<i>Vulpes lagopus</i>) cross into the marine environment (sea ice) during winter to access marine resources. Arctic foxes kill seal pups and scavenge seal carrion (often remains from polar bear <i>Ursus maritimus</i> kills), especially when rodent abundance is low. Terrestrial predator use of marine subsidies may strengthen the top-down control of tundra food webs, but this hypothesis remained untested. We evaluated tundra food web dynamics at the terrestrial–marine interface from an ecosystem-level perspective by assessing: (1) how winter environmental conditions affect rodent abundance and marine subsidy availability, (2) the response of the Arctic fox population to this seasonal food variability, and (3) the subsequent effects of Arctic foxes on Canada goose (<i>Branta canadensis interior</i>) reproduction. Arctic foxes responded numerically to rodent abundance, which was positively related to snow persistence. Arctic fox abundance was positively related to polar bear body condition metrics, which were used as a proxy for marine subsidy availability. Canada goose reproductive success, in turn, was negatively related to Arctic fox abundance. Long-term trends in goose reproduction and snow persistence also indicate an ongoing phenological mismatch between nesting initiation and spring onset. Our results reveal near-term apparent competition between rodents and geese through a shared predator, Arctic foxes, contrasting with prior studies evaluating rodent–goose–predator relationships. Moreover, we establish a link between tundra and sea ice food webs by demonstrating how seal availability can affect goose reproduction indirectly by increasing Arctic fox predation on goose nests via a population response of foxes to marine resources. These marine resources are often provisioned by polar bears, and with both Arctic foxes and polar bears undergoing long-term regional declines evidently driven by climate-related changes in prey abundance and availability, we contextualize our study within ongoing climate change and highlight the vulnerability of this likely widespread terrestrial–marine linkage in a warming Arctic.</p>","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://esajournals.onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.70204","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145261631","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}
Brendan D. Carson, Colin M. Orians, Elizabeth E. Crone
Viruses have the potential to impact host populations, but our picture of host–virus relationships is largely colored by virulent pathogens that lead to easily detectable epizootic events. Modern molecular methods have demonstrated that viruses are ubiquitous in animal populations, and the influence of these “cryptic” viruses is largely unexplored. Insects provide an ideal system to examine population-level impacts of novel, “cryptic” viruses—short generation times allow for meaningful population-level field studies over a relatively short timeframe, and their abundance and small size facilitate experimental manipulation across each life stage. Many insect species are capable of high population growth rates, potentially buffering them from pathogen-driven declines in the face of high pathogen prevalence. We explored the impacts of a recently detected non-occluded densovirus (Junonia coenia DV, JcDV) on the demography of a nymphalid butterfly, Euphydryas phaeton (Baltimore checkerspot). E. phaeton populations are known to have the capacity for rapid growth and to exhibit large, often unexplained population fluctuations. We used a field mesocosm experiment to measure the vital rates of E. phaeton under a range of levels of viral exposure over 2 years (2021 and 2022) and used these vital rates to parameterize a demographic model of population growth in each year. We found that JcDV reduced E. phaeton post-diapause larval survival, skewed sex ratios toward a male bias, and reduced fecundity in surviving females. JcDV reduced estimated population growth rates in both years, but only led to population decline in 2022. This increased impact was associated with a substantial regional drought, suggesting that the potential for this non-occluded virus to cause population decline is influenced by climatic factors. The findings of our controlled study parallel trends observed in a wild population of E. phaeton, supporting the hypothesis that JcDV can drive population decline. This study demonstrates that cryptic viruses likely influence butterfly population dynamics, especially when their effects are compounded with additional environmental stressors.
{"title":"Context-dependent effects of a cryptic virus on butterfly population dynamics","authors":"Brendan D. Carson, Colin M. Orians, Elizabeth E. Crone","doi":"10.1002/ecy.70199","DOIUrl":"10.1002/ecy.70199","url":null,"abstract":"<p>Viruses have the potential to impact host populations, but our picture of host–virus relationships is largely colored by virulent pathogens that lead to easily detectable epizootic events. Modern molecular methods have demonstrated that viruses are ubiquitous in animal populations, and the influence of these “cryptic” viruses is largely unexplored. Insects provide an ideal system to examine population-level impacts of novel, “cryptic” viruses—short generation times allow for meaningful population-level field studies over a relatively short timeframe, and their abundance and small size facilitate experimental manipulation across each life stage. Many insect species are capable of high population growth rates, potentially buffering them from pathogen-driven declines in the face of high pathogen prevalence. We explored the impacts of a recently detected non-occluded densovirus (<i>Junonia coenia</i> DV, JcDV) on the demography of a nymphalid butterfly, <i>Euphydryas phaeton</i> (Baltimore checkerspot). <i>E. phaeton</i> populations are known to have the capacity for rapid growth and to exhibit large, often unexplained population fluctuations. We used a field mesocosm experiment to measure the vital rates of <i>E. phaeton</i> under a range of levels of viral exposure over 2 years (2021 and 2022) and used these vital rates to parameterize a demographic model of population growth in each year. We found that JcDV reduced <i>E. phaeton</i> post-diapause larval survival, skewed sex ratios toward a male bias, and reduced fecundity in surviving females. JcDV reduced estimated population growth rates in both years, but only led to population decline in 2022. This increased impact was associated with a substantial regional drought, suggesting that the potential for this non-occluded virus to cause population decline is influenced by climatic factors. The findings of our controlled study parallel trends observed in a wild population of <i>E. phaeton</i>, supporting the hypothesis that JcDV can drive population decline. This study demonstrates that cryptic viruses likely influence butterfly population dynamics, especially when their effects are compounded with additional environmental stressors.</p>","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145277391","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Bo Meng, Alesia J. Hallmark, Timothy J. Ohlert, Pubin Hong, Scott L. Collins
Reordering of abundances among species is a common response in communities whether affected by anthropogenic drivers or natural disturbance. However, understanding how competitive relationships drive community dynamics under global environmental change remains limited, primarily due to uncertainties related to changes in species interactions and the scarcity of long-term observations. By combining long-term data and time series analysis tools, we quantified the compositional dynamics and causal interactions among functional groups of an arid grassland community under chronic nutrient enrichment for 15 years following wildfire. We hypothesized that chronic nutrient addition would promote species reordering among dominant grasses and subordinate annual forbs after wildfire, thereby increasing biomass and compositional variation over the long term. Contrary to expectations, while the abundance of the dominant grass Bouteloua eriopoda (black grama) declined immediately after the wildfire, the increase in annual forbs under N addition did not occur until a decade later. Convergent cross-mapping revealed that annuals were causally influenced by black grama abundance and maintained relatively lower abundance in control plots. However, with N addition, this causal interaction from black grama to annuals disappeared. Accordingly, temporal variability of biomass and community composition increased as the abundance of annuals rose. Combined with evidence of precipitation response, these results imply that the competitive advantage of perennial plants over annual forbs could serve as a stabilizing mechanism for community variability by limiting the response of annuals to precipitation fluctuations. However, this stabilizing process is disrupted by the cumulative effects of chronic nitrogen addition. This long-term experiment provides new insights into the destabilizing effects of community reordering, without changes in species richness, in response to anthropogenic nutrient loading.
{"title":"Species reordering increases community variability driven by chronic nutrient addition","authors":"Bo Meng, Alesia J. Hallmark, Timothy J. Ohlert, Pubin Hong, Scott L. Collins","doi":"10.1002/ecy.70227","DOIUrl":"10.1002/ecy.70227","url":null,"abstract":"<p>Reordering of abundances among species is a common response in communities whether affected by anthropogenic drivers or natural disturbance. However, understanding how competitive relationships drive community dynamics under global environmental change remains limited, primarily due to uncertainties related to changes in species interactions and the scarcity of long-term observations. By combining long-term data and time series analysis tools, we quantified the compositional dynamics and causal interactions among functional groups of an arid grassland community under chronic nutrient enrichment for 15 years following wildfire. We hypothesized that chronic nutrient addition would promote species reordering among dominant grasses and subordinate annual forbs after wildfire, thereby increasing biomass and compositional variation over the long term. Contrary to expectations, while the abundance of the dominant grass <i>Bouteloua eriopoda</i> (black grama) declined immediately after the wildfire, the increase in annual forbs under N addition did not occur until a decade later. Convergent cross-mapping revealed that annuals were causally influenced by black grama abundance and maintained relatively lower abundance in control plots. However, with N addition, this causal interaction from black grama to annuals disappeared. Accordingly, temporal variability of biomass and community composition increased as the abundance of annuals rose. Combined with evidence of precipitation response, these results imply that the competitive advantage of perennial plants over annual forbs could serve as a stabilizing mechanism for community variability by limiting the response of annuals to precipitation fluctuations. However, this stabilizing process is disrupted by the cumulative effects of chronic nitrogen addition. This long-term experiment provides new insights into the destabilizing effects of community reordering, without changes in species richness, in response to anthropogenic nutrient loading.</p>","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145260732","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Ryoshiro Wakiya, Masaru Sakai, Toshitaka N. Suzuki, Yosuke Kojima, Hikaru Itakura, Mari Matsuoka, Kenzo Kaifu
<p>Descriptions of terrestrial feeding in fishes are clues to understanding the origins and evolution of terrestrial tetrapods (Van Wassenbergh, <span>2019</span>). Terrestrial feeding behavior is currently known in five fish taxa: mudskippers (Colombini et al., <span>1995</span>), eel catfish (Huysentruyt et al., <span>2004</span>), reedfish (Van Wassenbergh et al., <span>2017</span>), blennies (Nieder, <span>2001</span>), and largescale foureyes (Brenner & Krumme, <span>2007</span>; Zahl et al., <span>1977</span>). Mudskippers, eel catfish, and reedfish commonly lift their trunks to capture terrestrial prey on land, and their unique pectoral fins or eel-like elongated bodies that sustain the trunk-lifting behaviors are considered keys to their achievement of terrestrial feeding (Van Wassenbergh et al., <span>2017</span>). However, whether anguillids, the representative elongated fish, can feed terrestrially is unknown. A recent study of the stomach contents of <i>Anguilla japonica</i> indicated that this eel is highly dependent on terrestrial cockroaches, centipedes, and semi-terrestrial freshwater crabs as prey, particularly in upper rivers (Wakiya & Mochioka, <span>2020</span>); however, the manner of predation is unknown. We recorded natural landing behavior in <i>A. marmorata</i>, another anguillid fish distributed in Japan, implying terrestrial feeding (Video S1). Here, we report the discovery of terrestrial feeding in <i>A. marmorata</i>. In behavioral experiments in which only terrestrial prey was available, all 10 tested individuals left the water and successfully caught the terrestrial prey (Figure 1).</p><p>In September 2018, we used electrofishing (Smith-Root Inc. LR-20B) in a 200-m downstream reach of a small stream (Kejin River) on Amami-Oshima Island, Kagoshima, Japan, to capture 10 <i>A. marmorata</i> individuals (total lengths: 312–536 mm) and observe terrestrial feeding directly. The eels were transported separately and stored in overflowing aquarium systems at Chuo University, Tokyo, Japan. The aquarium systems included aquatic and terrestrial spaces accessible to the eels (Figure 1); the water level was maintained at 24 cm. A security camera (QT914-4N4, Q. See) was placed in front of each experimental tank to record eel behavior for up to 10 consecutive days (191–238 h). The experimental systems were fully covered with a light shield, and the lights above the experimental tanks were turned on semidiurnally (12 h light and 12 h dark). During the experimental periods, no maintenance, such as water exchange, was performed. Three crickets (<i>Acheta domesticus</i>) were housed in each terrestrial space immediately after introducing the eels. The number of prey was maintained at three as much as possible, and dead prey was removed at daily checks. In total, 3713 landing behaviors were observed at a frequency of 0.471–3.512 times per hour; 3270 landing behaviors occurred during dark phases of the cycle. We defined landing b
{"title":"Amphibious feeding mode in an anguillid fish","authors":"Ryoshiro Wakiya, Masaru Sakai, Toshitaka N. Suzuki, Yosuke Kojima, Hikaru Itakura, Mari Matsuoka, Kenzo Kaifu","doi":"10.1002/ecy.70202","DOIUrl":"10.1002/ecy.70202","url":null,"abstract":"<p>Descriptions of terrestrial feeding in fishes are clues to understanding the origins and evolution of terrestrial tetrapods (Van Wassenbergh, <span>2019</span>). Terrestrial feeding behavior is currently known in five fish taxa: mudskippers (Colombini et al., <span>1995</span>), eel catfish (Huysentruyt et al., <span>2004</span>), reedfish (Van Wassenbergh et al., <span>2017</span>), blennies (Nieder, <span>2001</span>), and largescale foureyes (Brenner & Krumme, <span>2007</span>; Zahl et al., <span>1977</span>). Mudskippers, eel catfish, and reedfish commonly lift their trunks to capture terrestrial prey on land, and their unique pectoral fins or eel-like elongated bodies that sustain the trunk-lifting behaviors are considered keys to their achievement of terrestrial feeding (Van Wassenbergh et al., <span>2017</span>). However, whether anguillids, the representative elongated fish, can feed terrestrially is unknown. A recent study of the stomach contents of <i>Anguilla japonica</i> indicated that this eel is highly dependent on terrestrial cockroaches, centipedes, and semi-terrestrial freshwater crabs as prey, particularly in upper rivers (Wakiya & Mochioka, <span>2020</span>); however, the manner of predation is unknown. We recorded natural landing behavior in <i>A. marmorata</i>, another anguillid fish distributed in Japan, implying terrestrial feeding (Video S1). Here, we report the discovery of terrestrial feeding in <i>A. marmorata</i>. In behavioral experiments in which only terrestrial prey was available, all 10 tested individuals left the water and successfully caught the terrestrial prey (Figure 1).</p><p>In September 2018, we used electrofishing (Smith-Root Inc. LR-20B) in a 200-m downstream reach of a small stream (Kejin River) on Amami-Oshima Island, Kagoshima, Japan, to capture 10 <i>A. marmorata</i> individuals (total lengths: 312–536 mm) and observe terrestrial feeding directly. The eels were transported separately and stored in overflowing aquarium systems at Chuo University, Tokyo, Japan. The aquarium systems included aquatic and terrestrial spaces accessible to the eels (Figure 1); the water level was maintained at 24 cm. A security camera (QT914-4N4, Q. See) was placed in front of each experimental tank to record eel behavior for up to 10 consecutive days (191–238 h). The experimental systems were fully covered with a light shield, and the lights above the experimental tanks were turned on semidiurnally (12 h light and 12 h dark). During the experimental periods, no maintenance, such as water exchange, was performed. Three crickets (<i>Acheta domesticus</i>) were housed in each terrestrial space immediately after introducing the eels. The number of prey was maintained at three as much as possible, and dead prey was removed at daily checks. In total, 3713 landing behaviors were observed at a frequency of 0.471–3.512 times per hour; 3270 landing behaviors occurred during dark phases of the cycle. We defined landing b","PeriodicalId":11484,"journal":{"name":"Ecology","volume":"106 10","pages":""},"PeriodicalIF":4.3,"publicationDate":"2025-10-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://esajournals.onlinelibrary.wiley.com/doi/epdf/10.1002/ecy.70202","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145255727","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}