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    <title>eLife: latest articles by subject</title>
    <link>https://elifesciences.org</link>
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      <title>Cognitive simplicity drives collective route improvements in homing pigeons</title>
      <link>https://elifesciences.org/articles/108054</link>
      <description>Cognitive abilities are central to how animals navigate complex environments. Beyond individual cognition, group living can also enhance navigation by pooling individually acquired information. One way this may be achieved is by following experienced leaders, which requires recognizing expertise within group members. Alternatively, accurate decisions could also emerge without expert opinions, through simpler mechanisms like the ‘wisdom of crowds’ principle that average out individual biases. Consequently, collective navigation strategies range from cognitively complex to simple, and yet, the prevalence or interplay of different collective strategies in nature remains unexplored. In this study, we asked: what is the navigation mechanism, requiring minimal cognitive demands, that is necessary and sufficient to quantitatively replicate the experimental results of a 2017 study on homing pigeons (&lt;i&gt;Columba livia&lt;/i&gt;), which showed that sequential chains of bird pairs flying home—similar to a game of telephone—led to shorter homing routes compared to control birds flying individually or in fixed pairs. Our results show that the experimental data aligns closely with the simplest strategy—route averaging. Surprisingly, the complex mechanism of selectively propagating the best flight through social learning offered no additional advantage. We further observed that mixed strategies, although not supported by the experimental data, in theory combined advantages from both averaging and active selection of better routes, resulting in even greater performance. Hence, our results highlight the potential for future research to investigate selective pressures shaping the evolution of cultural learning and trade-offs among different decision mechanisms theoretically available to social animals in nature.</description>
      <author>shoubhik.banerjee001@umb.edu (Albert B Kao)</author>
      <author>shoubhik.banerjee001@umb.edu (Fritz A Francisco)</author>
      <author>shoubhik.banerjee001@umb.edu (Shoubhik Chandan Banerjee)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.108054</guid>
      <category>Ecology</category>
      <category>Physics of Living Systems</category>
      <pubDate>Tue, 26 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-26T00:00:00Z</dc:date>
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    <item>
      <title>Developmental constraints mediate the reversal of temperature effects on the autumn phenology of European beech after the summer solstice</title>
      <link>https://elifesciences.org/articles/107554</link>
      <description>Accurate projections of temperate tree growing seasons under climate change require representing developmental constraints that determine tree resource allocation. A phenological ‘switch point’ after the summer solstice (21 June) has been proposed, with pre-solstice warming advancing autumn phenology and post-solstice warming delaying it. We propose that this switch is flexible and occurs at the compensatory point between early-season development and late-season temperature effects. We performed trans-solstice climate manipulation experiments on potted European beech (&lt;i&gt;Fagus sylvatica&lt;/i&gt;) saplings to test (i) how spring leaf-out timing and June-August temperatures influence end-of-season timing (bud set and leaf senescence) and (ii) whether daytime and nighttime temperatures before and after the solstice have distinct effects. Bud set and senescence were tightly coupled (&lt;i&gt;R&lt;sup&gt;2&lt;/sup&gt;&lt;/i&gt;=0.49), with stronger bud responses. Each day of delayed leaf-out postponed bud set by 0.24±0.06 days and senescence by 0.22±0.08 days. July full-day cooling delayed autumn phenology in late-leafing individuals (bud set +4.9±2.6 days; senescence +3.1± 2.8 days) but had a negligible impact on early-leafing trees. August full-day cooling advanced both stages. Pre-solstice daytime cooling had no effect, while post-soltice daytime cooling advanced autumn phenology. Nighttime cooling consistently delayed bud set. These findings support the Solstice-as-Phenology-Switch model and highlight the central role of developmental progression in constraining growing seasons. Faster early-season development – especially under nighttime warming – moves trees past the switch earlier, increasing sensitivity to late-season cooling and thereby triggering earlier autumn phenology. Phenology models should incorporate these developmentally-mediated and diel-specific temperature responses.</description>
      <author>dominic.rebindaine@usys.ethz.ch (Constantin M Zohner)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Dominic Rebindaine)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Haozhi Ma)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Lidong Mo)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Raymo Bucher)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Susanne S Renner)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Thomas W Crowther)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Yibiao Zou)</author>
      <author>dominic.rebindaine@usys.ethz.ch (Zhaofei Wu)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107554</guid>
      <category>Ecology</category>
      <pubDate>Fri, 22 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-22T00:00:00Z</dc:date>
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    <item>
      <title>Full factorial construction of synthetic microbial communities</title>
      <link>https://elifesciences.org/articles/101906</link>
      <description>Constructing combinatorially complete species assemblages is often necessary to dissect the complexity of microbial interactions and to find optimal microbial consortia. At the moment, this is accomplished through either painstaking, labor-intensive liquid handling procedures, or through the use of state-of-the-art microfluidic devices. Here, we present a simple, rapid, low-cost, and highly accessible liquid handling methodology for assembling all possible combinations of a library of microbial strains, which can be implemented with basic laboratory equipment. To demonstrate the usefulness of this methodology, we construct a combinatorially complete set of consortia from a library of eight &lt;i&gt;Pseudomonas aeruginosa&lt;/i&gt; strains, and empirically measure the community-function landscape of biomass productivity, identify the highest-yield community, and dissect the interactions that lead to its optimal function. This easy-to-implement, inexpensive methodology will make the assembly of combinatorially complete microbial consortia easily accessible for all laboratories.</description>
      <author>alvaro.sanchez@usal.es (Alvaro Sanchez)</author>
      <author>alvaro.sanchez@usal.es (Andrea Arrabal)</author>
      <author>alvaro.sanchez@usal.es (Juan Diaz-Colunga)</author>
      <author>alvaro.sanchez@usal.es (Magdalena San Roman)</author>
      <author>alvaro.sanchez@usal.es (Pablo Catalan)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.101906</guid>
      <category>Ecology</category>
      <pubDate>Tue, 19 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-19T00:00:00Z</dc:date>
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    <item>
      <title>Rapid riparian ecosystem recovery in low-latitudinal North China following the end-Permian mass extinction</title>
      <link>https://elifesciences.org/articles/104205</link>
      <description>The greatest mass extinction at the end of the Permian, ca. 252 million years ago, led to a tropical dead zone on land and sea. The speed of recovery of life has been debated, whether fast or slow, and terrestrial ecosystems are much less understood than marine. Here, we show fast reestablishment of riparian ecosystems in low-latitude North China as little as ~2 million years after the end-Permian mass extinction. The initial ichnoassemblages in shallow lacustrine and fluvial facies of late Smithian age are monospecific, devoid of infaunalization, with apparent size reduction. In the following Spathian, relatively complex, multi-level, structured riverain ecosystems had been rebuilt including medium-sized carnivores, plant stems, root traces, increased ichnological complexity, and significantly increased infaunalization. Specifically, burrowing behavior had re-emerged as a key life strategy not only to minimize stressful climatic conditions, but possibly to escape predation.</description>
      <author>tianlibgeg@cug.edu.cn (Daoliang Chu)</author>
      <author>tianlibgeg@cug.edu.cn (Jinnan Tong)</author>
      <author>tianlibgeg@cug.edu.cn (Jun Liu)</author>
      <author>tianlibgeg@cug.edu.cn (Li Tian)</author>
      <author>tianlibgeg@cug.edu.cn (Michael J Benton)</author>
      <author>tianlibgeg@cug.edu.cn (Wenchao Shu)</author>
      <author>tianlibgeg@cug.edu.cn (Wenwei Guo)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.104205</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Mon, 18 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-18T00:00:00Z</dc:date>
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    <item>
      <title>Drift in individual behavioral phenotype as a strategy for unpredictable worlds</title>
      <link>https://elifesciences.org/articles/103585</link>
      <description>Individuals, even with matched genetics and environment, show substantial phenotypic variability. This variability may be part of a bet-hedging strategy, where populations express a range of phenotypes to ensure survival in unpredictable environments. In addition, phenotypic variability between individuals (‘bet-hedging’), individuals also show variability in their phenotype across time, even absent external cues. There are few evolutionary theories that explain random shifts in phenotype across an animal's life, which we term drift in individual phenotype. We use individuality in locomotor handedness in &lt;i&gt;Drosophila melanogaster&lt;/i&gt; to characterize both bet-hedging and drift. We use a continuous circling assay to show that handedness spontaneously changes over timescales ranging from seconds to the lifespan of a fly. We compare the amount of drift and bet-hedging across a number of different fly strains and show independent strain-specific differences in bet-hedging and drift. We show manipulation of serotonin changes the rate of drift, indicating a potential circuit substrate controlling drift. We then develop a theoretical framework for assessing the adaptive value of drift, demonstrating that drift may be adaptive for populations subject to selection pressures that fluctuate on timescales similar to the lifespan of an animal. We apply our model to real-world environmental signals and find patterns of fluctuations that favor random drift in behavioral phenotype, suggesting that drift may be adaptive under some real-world conditions. These results demonstrate that drift plays a role in driving variability in a population and may serve an adaptive role distinct from population-level bet-hedging.</description>
      <author>rtmaloney@coloradocollege.edu (Athena Q Ye)</author>
      <author>rtmaloney@coloradocollege.edu (Benjamin L de Bivort)</author>
      <author>rtmaloney@coloradocollege.edu (David M Zimmerman)</author>
      <author>rtmaloney@coloradocollege.edu (Nicole C Pittoors)</author>
      <author>rtmaloney@coloradocollege.edu (Ryan T Maloney)</author>
      <author>rtmaloney@coloradocollege.edu (Sam-Keny Saint-Pre)</author>
      <author>rtmaloney@coloradocollege.edu (Tom Alisch)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.103585</guid>
      <category>Ecology</category>
      <category>Neuroscience</category>
      <pubDate>Tue, 12 May 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-05-12T00:00:00Z</dc:date>
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    </item>
    <item>
      <title>Geomagnetic and visual cues guide seasonal migratory orientation in the nocturnal fall armyworm, the world’s most invasive insect</title>
      <link>https://elifesciences.org/articles/109098</link>
      <description>The mechanisms guiding nocturnal insect migration remain poorly understood. Although many species are thought to use the geomagnetic field, the sensory basis of magnetic orientation in insects has yet to be clarified. We developed an indoor experimental system to investigate the integration of geomagnetic and visual cues in the seasonal orientation of a globally distributed pest moth, the fall armyworm (&lt;i&gt;Spodoptera frugiperda&lt;/i&gt;), a highly invasive species which in the past decade has colonized almost all potentially habitable regions of the globe. Our results demonstrate that fall armyworms require both geomagnetic and visual cues for accurate migratory orientation, with visual cues being indispensable for magnetic orientation. When visual and geomagnetic cues are placed in conflict, moths become disoriented, although not immediately, indicating that sensory recognition of the conflict requires time to process. We also show that the absence of visual cues leads to a significant loss of flight stability, which likely explains the disruption in orientation. Our findings highlight that visual cues are critical for stable magnetic orientation in the fall armyworm, offering a basis for future investigations of visual-magnetic integration in noctuid migrants.</description>
      <author>hugao@njau.edu.cn (Bo-Ya Gao)</author>
      <author>hugao@njau.edu.cn (Dai-Hong Yu)</author>
      <author>hugao@njau.edu.cn (Eric Warrant)</author>
      <author>hugao@njau.edu.cn (Gao Hu)</author>
      <author>hugao@njau.edu.cn (Guijun Wan)</author>
      <author>hugao@njau.edu.cn (Hui Chen)</author>
      <author>hugao@njau.edu.cn (Jason W Chapman)</author>
      <author>hugao@njau.edu.cn (Yan Wu)</author>
      <author>hugao@njau.edu.cn (Yi-Bo Ma)</author>
      <author>hugao@njau.edu.cn (Yi Ji)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.109098</guid>
      <category>Ecology</category>
      <pubDate>Thu, 16 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-16T00:00:00Z</dc:date>
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    </item>
    <item>
      <title>New idtracker.ai rethinks multi-animal tracking as a representation learning problem to increase accuracy and reduce tracking time</title>
      <link>https://elifesciences.org/articles/107602</link>
      <description>idTracker and idtracker.ai approach multi-animal tracking from video as an image classification problem. For this classification, both rely on segments of video where all animals are visible to extract images and their identity labels. When these segments are too short, tracking can become slow and inaccurate and, if they are absent, tracking is impossible. Here, we introduce a new idtracker.ai that reframes multi-animal tracking as a representation learning problem rather than a classification task. Specifically, we apply contrastive learning to image pairs that, based on video structure, are known to belong to the same or different identities. This approach maps animal images into a representation space where they cluster by animal identity. As a result, the new idtracker.ai eliminates the need for video segments with all animals visible, is more accurate, and tracks up to 700 times faster.</description>
      <author>gonzalo.polavieja@neuro.fchampalimaud.org (Gonzalo de Polavieja)</author>
      <author>gonzalo.polavieja@neuro.fchampalimaud.org (Jordi Torrents)</author>
      <author>gonzalo.polavieja@neuro.fchampalimaud.org (Tiago Costa)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107602</guid>
      <category>Ecology</category>
      <category>Neuroscience</category>
      <pubDate>Wed, 15 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-15T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Adaptive variation in avian eggshell gas conductance and structure across elevational gradients?</title>
      <link>https://elifesciences.org/articles/85564</link>
      <description>Many tropical bird species have restricted elevational distributions, potentially limited by how environmental conditions affect physiological processes. While some studies have examined adult physiology across elevations, relatively little attention has been given to the structure and function of eggshells despite their critical role in regulating gas exchange during the vulnerable embryonic stage. At high elevations, dry air is expected to increase water loss from the egg, and natural selection may favor lower gas conductance to reduce desiccation risk. Structural variation in eggshells, such as increased shell thickness or reduced pore size and density, could serve as a mechanism to regulate gas diffusion. To test for adaptive variation in eggshell traits along elevational gradients, we measured water vapor conductance and used scanning electron microscopy (SEM) to examine eggshell structure in 197 bird species from the Andes. We found that water vapor conductance declined at high elevations across avian communities. However, structural changes in eggshells varied among bird families and did not vary in a predictable way with elevation, suggesting no relationship or divergent adaptive responses to shared selective pressures, particularly in shell thickness, pore density, and pore size. We propose that examining functional and structural eggshell traits can offer insight into species’ elevational limits and inform predictions about their responses to climate change.</description>
      <author>docampo@princeton.edu (Carlos Daniel Cadena)</author>
      <author>docampo@princeton.edu (David Ocampo)</author>
      <author>docampo@princeton.edu (Esteban Correa-Agudelo)</author>
      <author>docampo@princeton.edu (Gustavo A Londoño)</author>
      <author>docampo@princeton.edu (Marcela Hernández Hoyos)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.85564</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 14 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-14T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Fitness drivers of division of labor in vertebrates</title>
      <link>https://elifesciences.org/articles/105501</link>
      <description>Although division of labor as a means to increase productivity is a common feature in animal social groups, most previous studies have focused almost exclusively on eusocial insects with extreme task partitioning. Empirical evidence of division of labor in vertebrates is scarce, largely because we lack a theoretical framework to explore the conditions under which division of labor is likely to evolve in cooperatively breeding systems where helpers remain capable of breeding throughout their lifetime. By explicitly considering alternative helping tasks with varying fitness costs, we model how individual decisions on task specialization may influence the emergence of division of labor under both direct and indirect fitness benefits. Surprisingly, we find that direct survival benefits of living in larger groups are the primary force driving the evolution of cooperation to enhance group productivity, and that indirect fitness benefits derived from related group members are only a non-essential facilitator of more stable forms of division of labor in cooperative breeders. In addition, we find that division of labor in vertebrates is favored by harsh environments. Ultimately, our model not only makes key predictions that are consistent with existing empirical data, but also proposes novel avenues for new empirical work in vertebrate and invertebrate systems alike.</description>
      <author>igaru.13@gmail.com (Dustin R Rubenstein)</author>
      <author>igaru.13@gmail.com (Irene García-Ruiz)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.105501</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Wed, 08 Apr 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-04-08T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Cardenolide toxin diversity impacts monarch butterfly growth and sequestration</title>
      <link>https://elifesciences.org/articles/109003</link>
      <description>In coevolutionary interactions, host plants accrue novel chemical defenses that specialist herbivores counter by detoxification and sometimes sequestration. We recently found unusual nitrogen- and sulfur-containing (N,S-) cardenolides in some milkweeds—highly toxic compounds that monarch butterflies (&lt;i&gt;Danaus plexippus&lt;/i&gt;) detoxify during sequestration. We hypothesized that the N,S-cardenolides in &lt;i&gt;Asclepias curassavica&lt;/i&gt; (uscharin and voruscharin) would reduce caterpillar performance and sequestration more than other abundant related cardenolides (15-hydroxy-calotropin, frugoside, calactin). Cardenolides generally increased feeding relative to controls, but voruscharin was not stimulatory and substantially reduced growth efficiency. Exposure to either N,S-cardenolide produced the lowest sequestration and reduced sequestration efficiency, consistent with detoxification limiting toxin retention. We next tested whether toxin mixtures impose additional costs relative to individual compounds. We prepared two mixtures, one with equal concentrations of five cardenolides and a ‘realistic mixture’ reflecting natural proportions. Relative to the average of single compounds, mixtures reduced feeding, growth, sequestration, and sequestration efficiency, indicating phytochemical diversity effects exceeded expectations from an additive model. The two mixtures similarly reduced growth, but feeding on the realistic mixture yielded the lowest sequestration. We conclude that coevolution can produce highly specialized defense metabolites such as N,S-cardenolides that thwart even sequestering herbivores, and that phytochemical mixtures strengthen plant defense.</description>
      <author>aa337@cornell.edu (Amy P Hastings)</author>
      <author>aa337@cornell.edu (Anurag A Agrawal)</author>
      <author>aa337@cornell.edu (Paola Rubiano-Buitrago)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.109003</guid>
      <category>Ecology</category>
      <category>Plant Biology</category>
      <pubDate>Mon, 16 Mar 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-03-16T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Agent-based modeling reveals how bats navigate dense group emergences</title>
      <link>https://elifesciences.org/articles/105571</link>
      <description>Bats face a complex navigation challenge when emerging from densely populated roosts, where vast numbers take off at once in dark, confined spaces. Each bat must avoid collisions with walls and conspecifics while locating the exit, all amidst overlapping acoustic signals. This crowded environment creates the risk of acoustic jamming, in which the calls of neighboring bats interfere with echo detection, potentially obscuring vital information. Despite these challenges, bats navigate these conditions with remarkable success. Although bats have access to multiple sensory cues, here, we focused on whether echolocation alone could provide sufficient information for orientation under such high-interference conditions. To explore whether and how they manage this challenge, we developed a sensorimotor model that mimics the bats’ echolocation behavior under high-density conditions. Our model suggests that the problem of acoustic jamming may be less severe than previously assumed. Frequent calls with short inter-pulse intervals (IPI) increase the sensory input flow, allowing integration of echoic information across multiple calls. When combined with simple movement-guidance strategies—such as following walls and avoiding nearby obstacles—this accumulated information enables effective navigation in dense acoustic environments. Together, these findings demonstrate a plausible mechanism by which bats may overcome acoustic interference and underscore the role of signal redundancy in supporting robust echolocation-based navigation. Beyond advancing our understanding of bat behavior, they also offer valuable insights for swarm robotics and collective movement in complex environments.</description>
      <author>omer_mazar@yahoo.com (Omer Mazar)</author>
      <author>omer_mazar@yahoo.com (Yossi Yovel)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.105571</guid>
      <category>Computational and Systems Biology</category>
      <category>Ecology</category>
      <pubDate>Mon, 02 Mar 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-03-02T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>A sense of direction</title>
      <link>https://elifesciences.org/articles/110796</link>
      <description>Migratory moths use both magnetic and visual cues for navigation when travelling long distances in the dark.</description>
      <author>d.kishkinev@keele.ac.uk (Aleksandr Pakhomov)</author>
      <author>d.kishkinev@keele.ac.uk (Dmitry Kishkinev)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110796</guid>
      <category>Ecology</category>
      <pubDate>Mon, 02 Mar 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-03-02T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Rift Valley fever virus dynamics in a transhumant cattle system in The Gambia</title>
      <link>https://elifesciences.org/articles/107346</link>
      <description>Rift Valley fever (RVF) is a zoonotic disease of global concern, driven by environmental conditions, vector activity, and livestock mobility. Although RVF has been reported in The Gambia, its epidemiology remains poorly understood. This study developed a compartmental model to study RVF dynamics in the cattle population of the country. The model incorporated seasonally dynamic transmission parameters reflecting transhumant movement and ecological differences between two distinct ecoclimatic regions: the Sahelian area and the Gambia river. Parameterised using serological data linked to household survey data, the model predicted endemic RVF virus (RVFV) circulation within The Gambia and captured temporal infection trends that closely match empirical data. Weak decay rates of seropositivity were required to match predicted and observed age-seroprevalence. Results indicated sustained RVFV transmission during the dry season in the Gambia river eco-region, with a high risk of seasonal virus introductions to the Sahelian eco-region at the start of the wet season via the returning transhumant cattle. Our study highlighted the role of livestock mobility in RVFV epidemiology in The Gambia and the need for targeted control strategies that might include, for example, targeted cattle vaccination or application of topical insecticide treatments for transhumant herds.</description>
      <author>jarraessa@yahoo.com (Daniel T Haydon)</author>
      <author>jarraessa@yahoo.com (Divine Ekwem)</author>
      <author>jarraessa@yahoo.com (Essa Jarra)</author>
      <author>jarraessa@yahoo.com (Sarah Cleaveland)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107346</guid>
      <category>Ecology</category>
      <category>Epidemiology and Global Health</category>
      <pubDate>Fri, 27 Feb 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-02-27T00:00:00Z</dc:date>
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    </item>
    <item>
      <title>Kinematics and morphological correlates of descent strategies in arboreal mammals suggest early upright postures in euprimates</title>
      <link>https://elifesciences.org/articles/108268</link>
      <description>Ascending and descending sloping and vertical branches are critical for arboreal locomotion and likely played a major role in early primate evolution. While most studies have focused on ascent, descending behaviors also provide insight into the functional significance of arboreal adaptations. To test how descending vertical supports of varying diameters affect locomotor abilities, we quantified postural and kinematic features during descents and ascents on vertical supports in 21 eutherian and metatherian mammals and examined their relation to morphology. Primates showed greater variability in descent behaviors, using tail-first and side postures more often than other mammals, which predominantly descended head-first. Overall, animals adopted several kinematic adjustments to enhance stability during descent compared to ascent, including slower speeds, higher duty factors, and greater use of asymmetrical gaits. Additionally, vertical descent strategies reflected trade-offs among body mass, limb proportions, and head mass. Using a morphology-based model, we then inferred possible descent behaviors in 13 extinct euarchontoglires. Our results suggest that ancestral adaptations for vertical locomotion may have promoted frequent upright (head-up) postures in early primates.</description>
      <author>severine.toussaint@mnhn.fr (Dionisios Youlatos)</author>
      <author>severine.toussaint@mnhn.fr (John A Nyakatura)</author>
      <author>severine.toussaint@mnhn.fr (Severine LD Toussaint)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.108268</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 17 Feb 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-02-17T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Female moths incorporate plant acoustic emissions into their oviposition decision-making process</title>
      <link>https://elifesciences.org/articles/104700</link>
      <description>Insects rely on plants’ visual, chemical, tactile, and electrical cues when making various decisions. A recent study demonstrated that dehydrated plants emit ultrasonic sounds within the auditory sensitivity range of many moth species. In this study, we sought to determine whether insects also rely on plant acoustic signals when making decisions. We investigated whether female moths rely on ultrasonic clicks which are typically produced by dehydrated plants when deciding where to oviposit. In the absence of an actual plant, the moths indeed preferred to lay their eggs in proximity to acoustic signals which represent dehydrating plants. Tracking the moths’ behavior prior to the decision showed that they examined both sides of the arena and gradually spent more time on the acoustic-playback side. Interestingly, when actual plants were added to the arena, the oviposition preference was reversed and the moths preferred silent plants, which is in accordance with their a priori preference for hydrated plants. Deafening the moths eliminated their preference, confirming that the choice was based on hearing. Moreover, the presence of male moths, including their auditory signals, did not affect their oviposition decision, suggesting that the response was specific to plant sound emissions. We reveal evidence for a first acoustic interaction between moths and plants, but as plants emit various sounds, our findings hint at the existence of more currently unknown insect-plant acoustic interactions.</description>
      <author>ryaseltzer@gmail.com (Ahmed Afani)</author>
      <author>ryaseltzer@gmail.com (Dana Ment)</author>
      <author>ryaseltzer@gmail.com (Galina Levedev)</author>
      <author>ryaseltzer@gmail.com (Gayl Sharabi)</author>
      <author>ryaseltzer@gmail.com (Guy Zer Eshel)</author>
      <author>ryaseltzer@gmail.com (Ireen Atallah)</author>
      <author>ryaseltzer@gmail.com (Lilach Hadany)</author>
      <author>ryaseltzer@gmail.com (Maya Harari Gibli)</author>
      <author>ryaseltzer@gmail.com (Michael Davidovitz)</author>
      <author>ryaseltzer@gmail.com (Neta Shvil)</author>
      <author>ryaseltzer@gmail.com (Ofri Eitan)</author>
      <author>ryaseltzer@gmail.com (Omer Yinon)</author>
      <author>ryaseltzer@gmail.com (Rya Seltzer)</author>
      <author>ryaseltzer@gmail.com (Sabina Matveev)</author>
      <author>ryaseltzer@gmail.com (Sahar Hadad)</author>
      <author>ryaseltzer@gmail.com (Tal Ben Tov)</author>
      <author>ryaseltzer@gmail.com (Yossi Yovel)</author>
      <author>ryaseltzer@gmail.com (Yuval Shapira)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.104700</guid>
      <category>Ecology</category>
      <pubDate>Mon, 05 Jan 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-01-05T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Range geography and temperature variability explain cross-continental convergence in range and phenology shifts in a model insect taxon</title>
      <link>https://elifesciences.org/articles/101208</link>
      <description>Climate change may introduce conditions beyond species’ tolerances; to survive, species must avoid these extremes. Phenological shifts are one strategy, as species move their activity or life-history events in time to avoid extreme conditions. Species may also shift in space, moving their ranges poleward to escape extremes. However, whether species are more likely to exhibit one or both strategies, and whether this can be predicted based on a species’ functional traits, is unknown. Using a powerful macroecological dataset of European and North American odonate observations, we assessed range and phenology shifts between two time periods (1980–2002 and 2008–2018) to measure the strength and direction of the association between responses. Species with the greatest poleward range shifts also showed the largest phenological shifts toward earlier annual activity periods, with half of all species shifting in both space and time. This response was consistent across continents, despite highly divergent land use and biogeographical histories in these regions. Surprisingly, species’ range and phenology shifts were not related to functional traits; rather, southern species shifted their range limits more strongly, while increasing temperature variability hindered range shifts. By reducing risk through phenological shifts, the resulting larger populations may be more likely to disperse and expand species’ ranges. Species shifting in both space and time may be more resilient to extreme conditions, although further work integrating abundance data is needed. We also identified a small number of species (approximately 10%) that failed to shift at all; these species are likely to be particularly vulnerable to climate change and should be prioritized for conservation intervention.</description>
      <author>susan.ccgordon@gmail.com (Catherine Sirois-Delisle)</author>
      <author>susan.ccgordon@gmail.com (Jeremy Kerr)</author>
      <author>susan.ccgordon@gmail.com (Susan CC Gordon)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.101208</guid>
      <category>Ecology</category>
      <pubDate>Fri, 12 Dec 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-12-12T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Early experience affects foraging behavior of wild fruit bats more than their original behavioral predispositions</title>
      <link>https://elifesciences.org/articles/103220</link>
      <description>There are immense consistent inter-individual differences in animal behavior. While many studies have documented such behavioral differences, often referred to as individual personalities, little research has focused on the underlying causes and on determining whether they are innate or based on individual experience. Moreover, most studies on animal personalities have described consistent differences in behavior under laboratory conditions. We aimed to examine the impact of the early experienced environment on individual animal behavior, and to compare it to that of the individual’s original genetic predisposition. Additionally, we explored the correlation between personality traits measured indoors and the animal’s outdoor behavior. We studied Egyptian fruit bats, in which vast behavioral variability and plasticity have already been demonstrated. We raised bats in a captive colony under either enriched or impoverished environments and assessed their personality under controlled laboratory conditions. We then released the bats into the wild and tracked their foraging using GPS. Bats that had experienced an enriched environment during early life displayed increasing boldness and exploratory behavior when foraging outdoors, demonstrating how early-life experience can affect adult behavior. The individuals’ original predispositions did not predict their later foraging behavior. Our findings shed new light on the interplay between innate and experience-based effects on individual behavior.</description>
      <author>yossiyovel@gmail.com (Adi Rachum)</author>
      <author>yossiyovel@gmail.com (Aya Goldshtein)</author>
      <author>yossiyovel@gmail.com (Lee M Harten)</author>
      <author>yossiyovel@gmail.com (Nesim Gonceer)</author>
      <author>yossiyovel@gmail.com (Reut Assa)</author>
      <author>yossiyovel@gmail.com (Xing Chen)</author>
      <author>yossiyovel@gmail.com (Yossi Yovel)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.103220</guid>
      <category>Ecology</category>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-11-11T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Individual recognition in a jumping spider (&lt;i&gt;Phidippus regius&lt;/i&gt;)</title>
      <link>https://elifesciences.org/articles/97146</link>
      <description>Individual recognition is conceptually complex and computationally intense, leading to the general assumption that this social knowledge is solely present in vertebrates with larger brains, while miniature-brained animals in differentiating societies eschew the evolutionary pressure for individual recognition by evolving computationally less demanding class-level recognition, such as kin, social rank, or mate recognition. Arguably, this social knowledge is restricted to species with a degree of sociality (sensu Wilson, 2000, for a review Gherardi et al., 2012). Here, we show the exception to this rule in a non-social arthropod species, the jumping spider &lt;i&gt;Phidippus regius&lt;/i&gt;. Using a habituation-dishabituation paradigm, we visually confronted pairs of spatially separated spiders with each other and measured the ‘interest’ of one spider towards the other. The spiders exhibited high interest upon initial encounter of an individual, reflected in mutual approach behaviour, but adapted towards that individual when it reoccurred in the subsequent trial, indicated by their preference of staying farther apart. In contrast, spiders exhibited a rebound from habituation, reflected in mutual approach behaviour, when a different individual occurred in the subsequent trial, indicating the ability to tell apart spiders’ identities. These results suggest that &lt;i&gt;P. regius&lt;/i&gt; is capable of individual recognition based on long-term memory.</description>
      <author>christoph.d.dahl@gmail.com (Christoph D Dahl)</author>
      <author>christoph.d.dahl@gmail.com (Yaling Cheng)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.97146</guid>
      <category>Ecology</category>
      <category>Neuroscience</category>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-11-11T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Assessing plant phenological changes based on drivers of spring phenology</title>
      <link>https://elifesciences.org/articles/106655</link>
      <description>Understanding plant phenological responses to climate warming is essential for predicting shifts in plant communities and ecosystems. However, this remains challenging when sensitivity analyses overlook the underlying drivers of spring phenology. In this article, we present a new measure &lt;i&gt;phenological lag&lt;/i&gt; to quantify the overall effect of phenological constraints, including insufficient winter chilling, photoperiod, and environmental stresses, based on observed response and that expected from species-specific changes in spring temperatures, that is, changes in spring forcing (degree days) from warming and average temperature at budburst with the warmer climate. We applied this new analytical framework to a global dataset with 980 species and 1527 responses to synthesize observed changes in spring budburst (leafing or flowering) and investigate the mechanisms of differential phenological responses reported previously. We found longer phenological lags with experimental studies and native plants in flowering, likely due to a more stressful environment associated with warmer and drier climate. Smaller forcing changes were mainly responsible for the smaller responses in leafing and flowering in the boreal region (compared to the temperate region) and in grass leafing (compared to trees and shrubs). Higher budburst temperatures also contributed to the smaller responses in flowering for experimental studies and with herbs and grasses. The effects of altitude, latitude, mean annual temperature (MAT), and average spring temperature change were minor (all combined &amp;lt;2.5% variations), while those of photoperiod and long-term precipitation were not significant in influencing spring phenology. Our method helps to determine mechanisms responsible for changes in spring phenology and differences in plant phenological responses.</description>
      <author>rongzhou.man@ontario.ca (Jing Tao)</author>
      <author>rongzhou.man@ontario.ca (Qing-Lai Dang)</author>
      <author>rongzhou.man@ontario.ca (Rongzhou Man)</author>
      <author>rongzhou.man@ontario.ca (Stephen J Mayor)</author>
      <author>rongzhou.man@ontario.ca (Xiaoqi Ye)</author>
      <author>rongzhou.man@ontario.ca (Xiuli Chu)</author>
      <author>rongzhou.man@ontario.ca (Yong Jiang)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.106655</guid>
      <category>Ecology</category>
      <pubDate>Tue, 11 Nov 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-11-11T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Birds migrate longitudinally in response to the resultant Asian monsoons of the Qinghai-Tibet Plateau uplift</title>
      <link>https://elifesciences.org/articles/103971</link>
      <description>The uplift of the Qinghai-Tibet Plateau is one of the greatest geological events on Earth, pivotally shaping biogeographic patterns across continents, especially for migratory species that need to overcome topographical barriers to fulfil their annual circle. However, how the uplift influences animal migration strategies remains largely unclear. We compare the current flyways of 50 avian species migrating across the plateau with those reconstructed before the uplift as a counterfactual. We find that the major effect of the plateau uplift is changing avian migratory directions from the latitudinal to the longitudinal. The monsoon system generated by the uplift rather than the high elevation per se shapes those changes. These findings unveil how an important global geological event has influenced biogeographic patterns of migratory birds, yielding testable hypotheses for how observed avian distributions emerge.</description>
      <author>zhanxj@ioz.ac.cn (Ran Zhang)</author>
      <author>zhanxj@ioz.ac.cn (Wenyuan Zhang)</author>
      <author>zhanxj@ioz.ac.cn (Xiangjiang Zhan)</author>
      <author>zhanxj@ioz.ac.cn (Yangkang Chen)</author>
      <author>zhanxj@ioz.ac.cn (Zhongru Gu)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.103971</guid>
      <category>Ecology</category>
      <pubDate>Wed, 05 Nov 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-11-05T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>&lt;i&gt;Desmodium&lt;/i&gt; volatiles in ‘push-pull’ cropping systems and protection against the fall armyworm, &lt;i&gt;Spodoptera frugiperda&lt;/i&gt;</title>
      <link>https://elifesciences.org/articles/100981</link>
      <description>Push-pull systems for sustainable pest management combine repellent stimuli from intercrops (‘push’) and attractive stimuli from border plants (‘pull’) to repel herbivorous insects from a main crop and attract the herbivores’ natural enemies. The most widespread implementation, intercropping the legume &lt;i&gt;Desmodium&lt;/i&gt; with maize surrounded by border grass, reduces damage from the invasive fall armyworm (FAW) &lt;i&gt;Spodoptera frugiperda&lt;/i&gt;. While initial research indicated that &lt;i&gt;Desmodium&lt;/i&gt; volatiles can dampen the attraction of FAW to maize, a recent study recovered very low volatile emission from the commonly used &lt;i&gt;D. intortum&lt;/i&gt; and found that the &lt;i&gt;D. intortum&lt;/i&gt; headspace did not reduce FAW oviposition on maize (Erdei et al., 2024). Here, we detect volatiles from the headspace of two &lt;i&gt;Desmodium&lt;/i&gt; species sampled within the activity window of FAW: &lt;i&gt;D. intortum&lt;/i&gt; and the more recently adopted &lt;i&gt;D. incanum&lt;/i&gt;; and we present the behavior of gravid FAW moths in bioassays. We detected 25 volatiles from field-grown &lt;i&gt;Desmodium&lt;/i&gt;, many in the headspaces of both species, including volatiles previously reported to repel lepidopteran herbivores. In cage oviposition assays, FAW moths preferred to oviposit on maize over &lt;i&gt;Desmodium&lt;/i&gt;, but not on maize further from, versus closer to &lt;i&gt;Desmodium&lt;/i&gt; plants that were inaccessible to the moths, but sharing headspace. In flight tunnel assays, moths approached the headspace of maize more than shared headspaces of maize and &lt;i&gt;Desmodium&lt;/i&gt;, but pairwise differences were often insignificant. Thus, headspaces of &lt;i&gt;Desmodium&lt;/i&gt; species include volatiles that could repel FAW moths, and gravid moths were generally more attracted to maize and its headspace than to either &lt;i&gt;Desmodium&lt;/i&gt; species or mixed maize-&lt;i&gt;Desmodium&lt;/i&gt; headspaces. However, our results suggest that direct effects of &lt;i&gt;Desmodium&lt;/i&gt; volatiles on FAW behavior are insufficient to explain reduced FAW infestation of maize under push-pull cultivation.</description>
      <author>daria.odermatt@bluewin.ch (Amanuel Tamiru)</author>
      <author>daria.odermatt@bluewin.ch (Bernhard Schmid)</author>
      <author>daria.odermatt@bluewin.ch (Collins O Onjura)</author>
      <author>daria.odermatt@bluewin.ch (Daniel M Mutyambai)</author>
      <author>daria.odermatt@bluewin.ch (Daria M Odermatt)</author>
      <author>daria.odermatt@bluewin.ch (Frank Chidawanyika)</author>
      <author>daria.odermatt@bluewin.ch (Luiz A Domeignoz Horta)</author>
      <author>daria.odermatt@bluewin.ch (Meredith C Schuman)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.100981</guid>
      <category>Ecology</category>
      <pubDate>Thu, 09 Oct 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-10-09T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Partitioning changes in ecosystem productivity by effects of species interactions in biodiversity experiments</title>
      <link>https://elifesciences.org/articles/98073</link>
      <description>Species interactions affect ecosystem productivity. Positive interactions (resource partitioning and facilitation) increase productivity while negative interactions (species interference) decrease productivity relative to the null expectations defined by monoculture yields. Effects of competitive interactions (resource competition) can be either positive or negative. Distinguishing effects of species interactions is therefore difficult, if not impossible, with current biodiversity experiments involving mixtures and full density monocultures. To partition changes in ecosystem productivity by effects of species interactions, we modify null expectations with competitive growth responses, i.e., proportional changes in individual size (biomass or volume) expected in mixture based on species differences in growth and competitive ability. We use partial density (species density in mixture) monocultures and the competitive exclusion principle to determine maximum competitive growth responses and full density monoculture yields to measure species ability to achieve maximum competitive growth responses in mixture. Deviations of observed yields from competitive expectations represent the effects of positive/negative species interactions, while the differences between competitive and null expectations reflect the effects of competitive interactions. We demonstrate the effectiveness of our competitive partitioning model in distinguishing effects of species interactions using both simulated and experimental species mixtures. Our competitive partitioning model enables meaningful assessments of species interactions at both species and community levels and helps disentangle underlying mechanisms of species interactions responsible for changes in ecosystem productivity and identify species mixtures that maximize positive effects.</description>
      <author>rongzhou.man@ontario.ca (Charles A Nock)</author>
      <author>rongzhou.man@ontario.ca (Cyrille Violle)</author>
      <author>rongzhou.man@ontario.ca (Eric B Searle)</author>
      <author>rongzhou.man@ontario.ca (Grégoire T Freschet)</author>
      <author>rongzhou.man@ontario.ca (Hua Yang)</author>
      <author>rongzhou.man@ontario.ca (Jing Tao)</author>
      <author>rongzhou.man@ontario.ca (Ji Zheng)</author>
      <author>rongzhou.man@ontario.ca (Rongzhou Man)</author>
      <author>rongzhou.man@ontario.ca (Shongming Huang)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.98073</guid>
      <category>Ecology</category>
      <pubDate>Thu, 09 Oct 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-10-09T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Pesticide-induced resurgence in brown planthoppers is mediated by action on a suite of genes that promote juvenile hormone biosynthesis and female fecundity</title>
      <link>https://elifesciences.org/articles/91774</link>
      <description>Pesticide-induced resurgence, increases in pest insect populations following pesticide application, is a serious threat to the sustainable control of many highly damaging crop pests. Resurgence can result from pesticide-enhanced pest reproduction; however, the molecular mechanisms mediating this process remain unresolved. Here we show that brown planthopper (BPH) resurgence in rice crops following exposure to sublethal doses of the pesticide emamectin benzoate (EB) results from the coordinated action of a suite of genes that regulate juvenile hormone (JH) levels, resulting in increased JH titer in adult females and enhanced fecundity. We demonstrate that EB treatment at sublethal levels results in profound changes in female BPH fitness, including increased egg maturation and oviposition. This enhanced reproductive fitness results from the EB-mediated upregulation of key genes involved in the regulation of JH, including &lt;i&gt;JHAMT and Kr-h1&lt;/i&gt; and the downregulation of allatostatin (&lt;i&gt;AstA&lt;/i&gt;) and allatostatin receptor (&lt;i&gt;AstAR&lt;/i&gt;) expression. AstA signaling is known to inhibit the production of JH in the corpora allata and hence EB exposure diminishes this inhibitory action. We find that the changes in gene expression following EB exposure are caused by the allosteric action of this insecticide on its molecular target, the glutamate-gated chloride channel (GluClα). Collectively, these results provide mechanistic insights into the regulation of negative pesticide-induced responses in insects and reveal some key actors involved in the JH-signaling pathway that underpin pesticide resurgence.</description>
      <author>wusf@njau.edu.cn (Chris Bass)</author>
      <author>wusf@njau.edu.cn (Congfen Gao)</author>
      <author>wusf@njau.edu.cn (Dick R Nässel)</author>
      <author>wusf@njau.edu.cn (Ji-Yang Xing)</author>
      <author>wusf@njau.edu.cn (Shao-Cong Su)</author>
      <author>wusf@njau.edu.cn (Shun-Fan Wu)</author>
      <author>wusf@njau.edu.cn (Yang Gao)</author>
      <author>wusf@njau.edu.cn (Zhao-Yu Liu)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.91774</guid>
      <category>Ecology</category>
      <pubDate>Tue, 30 Sep 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-09-30T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Strip cropping shows promising increases in ground beetle community diversity compared to monocultures</title>
      <link>https://elifesciences.org/articles/104762</link>
      <description>Global biodiversity is declining at an unprecedented rate, with agriculture as one of the major drivers. There is mounting evidence that intercropping can increase insect biodiversity while maintaining or increasing yield. Yet, intercropping is often considered impractical for mechanized farming systems. Strip cropping is a type of intercropping that is compatible with standard farm machinery and has been pioneered by Dutch farmers since 2014. Here, we present ground beetle data from four organically managed experimental farms across four years. Ground beetles are sensitive to changes in habitats and disturbances, and hold keystone positions in agroecosystem food webs. We show that strip cropping systems can enhance ground beetle biodiversity, while other studies showed that these increases have been achieved without incurring major yield loss. Strip-cropped fields had on average 15% more ground beetle species and 30% more individuals than monocultural fields. The higher ground beetle richness in strip crops was explained by the merger of crop-related ground beetle communities, rather than by ground beetle species unique to strip cropping systems. The increase in field-level beetle species richness in organic agriculture through strip cropping approached increases found for other readily deployed biodiversity conservation methods, like shifting from conventional to organic agriculture (+19% –+23%). This indicates that strip cropping is a potentially useful tool supporting ground beetle biodiversity in agricultural fields without compromising food production.</description>
      <author>luuk.croijmans@wur.nl (Dirk F van Apeldoorn)</author>
      <author>luuk.croijmans@wur.nl (Erik H Poelman)</author>
      <author>luuk.croijmans@wur.nl (Felix JJA Bianchi)</author>
      <author>luuk.croijmans@wur.nl (Fogelina Cuperus)</author>
      <author>luuk.croijmans@wur.nl (Luuk Croijmans)</author>
      <author>luuk.croijmans@wur.nl (Walter AH Rossing)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.104762</guid>
      <category>Ecology</category>
      <category>Plant Biology</category>
      <pubDate>Tue, 23 Sep 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-09-23T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Risk-taking incentives predict aggression heuristics in female gorillas</title>
      <link>https://elifesciences.org/articles/107093</link>
      <description>Competition is commonly reflected in aggressive interactions among groupmates as individuals try to attain or maintain higher social ranks that can offer them better access to critical resources. In this study, we investigate the factors that can shift competitive incentives against higher- or lower-ranking groupmates, that is, more or less powerful individuals. We use a long-term behavioural data set on five wild groups of the two gorilla species starting in 1998, and we show that most aggression is directed from higher- to lower-ranking adult females close in rank, highlighting rank-reinforcement incentives. Yet, females directed 42% of aggression to higher-ranking females than themselves. Females targeted groupmates of higher rank with increasing number of males in the group, suggesting that males might buffer female–female aggression risk. Contrarily, they targeted females of lower rank with increasing number of females in the group, potentially because this is a low-risk option that females prefer when they have access to a larger pool of competitors to choose from. Lactating and pregnant females, especially those in the latest stage of pregnancy, targeted groupmates of higher rank than the groupmates that cycling females targeted, suggesting that energetic needs may motivate females to risk confrontation with more powerful rivals. Our study provides critical insights into the evolution of competitive behaviour, showing that aggression heuristics, the simple rules that animals use to guide their aggressive interactions, are not merely species-specific but also dependent on the conditions that populations and individuals experience.</description>
      <author>nismit@utu.fi (Martha M Robbins)</author>
      <author>nismit@utu.fi (Nikolaos Smit)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.107093</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Fri, 22 Aug 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-08-22T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Weak evidence for heritable changes in response to selection by aphids in &lt;i&gt;Arabidopsis&lt;/i&gt; accessions</title>
      <link>https://elifesciences.org/articles/106930</link>
      <description>In plants, transgenerational inheritance of certain epialleles has been observed but experimental evidence for selection of epigenetic variation independent of genetic variation is scarce. We extended an experiment simulating selection in response to herbivory in &lt;i&gt;Arabidopsis thaliana&lt;/i&gt; to assess a potential contribution of epigenetic variation to the selected phenotypes within three accessions. To minimize maternal effects, we grew offspring from replicate populations and their ancestors for two generations in a common environment and assessed the phenotypes in the second generation. We found weak evidence for the selection of epigenetic variation: bolting time differed significantly in one accession. Significant differences between maternal lines suggested random residual or novel genetic and/or epigenetic variation. Our results are in conflict with those of a recent study reporting that environment-induced heritable variation is common in &lt;i&gt;Arabidopsis&lt;/i&gt;. Reanalyzing the data from that study showed that the reported findings resulted from a mix-up of accessions and, thus, reflected genetic rather than epigenetic variation between accessions. To avoid future misinterpretations of studies investigating epigenetic inheritance, we provide guidelines to design experiments that clearly differentiate between epigenetic and genetic variation and distinguish standing variation from de novo variation acquired during an experiment.</description>
      <author>grossnik@botinst.uzh.ch (Bernhard Schmid)</author>
      <author>grossnik@botinst.uzh.ch (Klara Kropivšek)</author>
      <author>grossnik@botinst.uzh.ch (Marc W Schmid)</author>
      <author>grossnik@botinst.uzh.ch (Samuel E Wuest)</author>
      <author>grossnik@botinst.uzh.ch (Ueli Grossniklaus)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.106930</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Tue, 12 Aug 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-08-12T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Loss of olfaction reduces caterpillar performance and increases susceptibility to a natural enemy</title>
      <link>https://elifesciences.org/articles/105585</link>
      <description>Insect herbivores such as caterpillars are under strong selection pressure from natural enemies, especially parasitoid wasps. Although the role of olfaction in host-plant seeking has been investigated in great detail in parasitoids and adult lepidopterans, the caterpillar olfactory system and its significance in tri-trophic interactions remain poorly understood. In this study, we investigated the olfactory system of &lt;i&gt;Pieris brassicae&lt;/i&gt; caterpillars and the importance of olfactory information in the interactions among this herbivore, its host-plant &lt;i&gt;Brassica oleracea&lt;/i&gt;, and its primary natural enemy &lt;i&gt;Cotesia glomerata&lt;/i&gt;. To examine the role of olfaction, we utilized CRISPR/Cas9 to knockout (KO) the odorant receptor co-receptor (&lt;i&gt;Orco&lt;/i&gt;). This KO impaired olfactory detection and primary processing in the brain. &lt;i&gt;Orco&lt;/i&gt; KO caterpillars exhibited reduced weight and lost preference for their optimal food plants. Interestingly, the KO caterpillars also experienced reduced weight when challenged by the parasitoid &lt;i&gt;C. glomerata&lt;/i&gt; whose ovipositor had been removed, and the mortality of the KO caterpillars under the attack of unmanipulated parasitoids increased. We then investigated the behavior of &lt;i&gt;P. brassicae&lt;/i&gt; caterpillars in response to volatiles from plants attacked by conspecific caterpillars and volatiles from plants on which the caterpillars were themselves attacked by &lt;i&gt;C. glomerata&lt;/i&gt;. After analyzing the volatile compounds involved in these interactions, we concluded that olfactory information enables caterpillars to locate suitable food sources more efficiently as well as to select enemy-free spaces. Our results reveal the crucial role of olfaction in caterpillar feeding and natural-enemy avoidance, highlighting the significance of chemoreceptor genes in shaping ecological interactions.</description>
      <author>alexander.haverkamp@wur.nl (Alexander Haverkamp)</author>
      <author>alexander.haverkamp@wur.nl (Berhane T Weldegergis)</author>
      <author>alexander.haverkamp@wur.nl (Hans M Smid)</author>
      <author>alexander.haverkamp@wur.nl (Liana O Greenberg)</author>
      <author>alexander.haverkamp@wur.nl (Maarten Jongsma)</author>
      <author>alexander.haverkamp@wur.nl (Marcel Dicke)</author>
      <author>alexander.haverkamp@wur.nl (Qi Wang)</author>
      <author>alexander.haverkamp@wur.nl (Yufei Jia)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.105585</guid>
      <category>Ecology</category>
      <pubDate>Fri, 01 Aug 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-08-01T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <item>
      <title>Effects of parental care on skin microbial community composition in poison frogs</title>
      <link>https://elifesciences.org/articles/103331</link>
      <description> Parent-offspring interactions constitute the first contact of many newborns with their environment, priming community assembly of microbes through priority effects and shaping host health and disease. Microbe acquisition during parental care is well studied in humans and agriculturally relevant species but remains poorly understood in other vertebrate groups, such as amphibians. Here, we investigate vertical transmission of skin microbiota in poison frogs (&lt;i&gt;Dendrobatidae&lt;/i&gt;), where fathers transport tadpoles piggyback-style from terrestrial clutches to aquatic nurseries. We found that substantial bacterial colonization of embryos begins after hatching, suggesting that the vitelline envelope acts as a microbial barrier. A cross-foster experiment demonstrated that poison frogs performing tadpole transport serve as a source of skin microbes for tadpoles on their back. To study how transport impacts skin communities of tadpoles in an ecologically relevant setting, we sampled sympatric species that do or do not exhibit tadpole transport in their natural habitat. We did not find a higher degree of similarity between microbial communities of tadpoles and adults in species that transport their offspring compared to those that do not. Similarly, communities of tadpoles were no more similar to their caregiver than to unrelated adults, indicating that most caregiver-associated microbes do not remain in tadpole communities long-term. Nonetheless, some taxa persisted on tadpoles over development. This study is the first to demonstrate that offspring transport facilitates transmission of parental skin microbes in anurans.</description>
      <author>fi5cher@stanford.edu (Anna Robaczewska)</author>
      <author>fi5cher@stanford.edu (David A Relman)</author>
      <author>fi5cher@stanford.edu (Elizabeth K Costello)</author>
      <author>fi5cher@stanford.edu (Gaelle Raboisson)</author>
      <author>fi5cher@stanford.edu (Katherine S Xue)</author>
      <author>fi5cher@stanford.edu (Lauren A O'Connell)</author>
      <author>fi5cher@stanford.edu (Mai Dvorak)</author>
      <author>fi5cher@stanford.edu (Marie-Therese Fischer)</author>
      <author>fi5cher@stanford.edu (Stephanie N Caty)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.103331</guid>
      <category>Ecology</category>
      <category>Microbiology and Infectious Disease</category>
      <pubDate>Thu, 31 Jul 2025 00:00:00 +0000</pubDate>
      <dc:date>2025-07-31T00:00:00Z</dc:date>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
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