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    <title>eLife: latest articles by subject</title>
    <link>https://elifesciences.org</link>
    <description>Articles published by eLife, filtered by given subjects</description>
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      <title>Scanning and active sampling behaviours emerge from conserved insect neural circuits</title>
      <link>https://elifesciences.org/articles/110165</link>
      <description>Navigating insects often pause and rotate to sample their surroundings, behaviours termed scanning. These and other active sampling behaviours embody navigational uncertainty and are key for spatial learning, yet their neural basis remains unclear and existing models impose scanning behaviours rather than explaining its emergence. Here, we show that desert ants’ scanning dynamics can emerge spontaneously from the same conserved neural circuits used for goal-directed navigation, without requiring a specialised scanning module. We built a biologically grounded model combining central complex steering and lateral accessory lobe oscillators and added a downstream stochastic inhibition of forward speed. This minimal system produced diverse, realistic scan dynamics; saccades, fixations, and reversals, whose features were qualitatively compared to high-speed video recordings of &lt;i&gt;Melophorus bagoti&lt;/i&gt; scanning. Detailed analysis of these natural scans confirmed model predictions, including how scan structure depends on oscillator phase, goal-heading deviation, and navigational uncertainty. Furthermore, the model reveals that simple modulation of forward speed unifies a broad range of behaviours across ant species, from dashes to smooth oscillatory trajectories to pirouettes and voltes. Crucially, this model suggests a distributed control principle where forward speed acts as a single adjustable parameter, for both individuals and through evolution, to regulate the balance between goal-driven exploitation and information-seeking exploration.</description>
      <author>freascody@gmail.com (Antoine Wystrach)</author>
      <author>freascody@gmail.com (Cody A Freas)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110165</guid>
      <category>Ecology</category>
      <pubDate>Tue, 06 Oct 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-10-06T00:00:00Z</dc:date>
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    <item>
      <title>Machine learning of honey bee olfactory behavior identifies repellent odorants in free-flying bees in the field</title>
      <link>https://elifesciences.org/articles/104831</link>
      <description>Preventing beneficial insects like honey bees (&lt;i&gt;Apis mellifera&lt;/i&gt;) from contacting pesticides on crops using odorants could counter current pollinator declines. However, the discovery of behaviorally aversive odorants is impeded by the complexity of the honey bee olfactory system where &amp;gt;170 olfactory receptors detect volatiles and generate valence. To solve this systems-level challenge, we generated a machine-learning model to predict aversive valence from chemical structure using published olfactory behavior data in honey bees. We refine the predictive model by generating species-level behavioral data for honey bees and &lt;i&gt;Drosophila&lt;/i&gt; on an initial set of novel predicted repellents. The improved second computational model was then used to screen a chemical space of &amp;gt;50 million compounds and identify &amp;gt;130 repellent candidates. Behavioral validation using honey bees in the laboratory shows a high predictive success. Additional testing of the top seven candidates using freely foraging honey bees in a field assay confirmed strong repellency, thus predicting a high probability to repel foraging bees from pesticide-treated crops. Machine learning, with iterative testing and modeling, therefore provides a powerful approach for rational discovery of aversive volatiles for control of insects for which limited data is available.</description>
      <author>anand.ray@ucr.edu (Anandasankar Ray)</author>
      <author>anand.ray@ucr.edu (Barbara F Baer-Imhoof)</author>
      <author>anand.ray@ucr.edu (Boris Baer)</author>
      <author>anand.ray@ucr.edu (Joel Kowalewski)</author>
      <author>anand.ray@ucr.edu (Matthew Luy)</author>
      <author>anand.ray@ucr.edu (Payton DePalma)</author>
      <author>anand.ray@ucr.edu (Tom Guda)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.104831</guid>
      <category>Ecology</category>
      <category>Neuroscience</category>
      <pubDate>Wed, 23 Sep 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-09-23T00:00:00Z</dc:date>
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    </item>
    <item>
      <title>Asymmetric introgression and thermal advantage jointly drive climate-mediated lineage turnover in a mixed-ploidy reed</title>
      <link>https://elifesciences.org/articles/112160</link>
      <description>Species distribution forecasts often ignore intraspecific genetic variation, potentially missing climate-driven lineage shifts within native ranges. We integrated population genomics (495 individuals), common-garden experiments across four sites, and species distribution modeling (837 records) for three genetic lineages of &lt;i&gt;Phragmites australis&lt;/i&gt; in China. The octoploid FEAU lineage (haplotype P) showed superior heat tolerance, with &lt;i&gt;T&lt;sub&gt;crit&lt;/sub&gt;&lt;/i&gt; 1.3 °C higher and &lt;i&gt;T&lt;sub&gt;50&lt;/sub&gt;&lt;/i&gt; 0.8 °C higher than the cold-adapted tetraploid CN lineage (haplotypes O/M), and produced greater total biomass in three of four gardens. Genomic analyses revealed bidirectional but asymmetric introgression; admixed individuals exhibited a significant bias toward FEAU ancestry (61.1%), consistent with preferential backcrossing to the octoploid parent. Under the high-emission scenario SSP5-8.5 by 2070, highly suitable habitat for FEAU expanded by 18.6%, whereas CN showed a smaller relative increase, and the subtropical SW lineage remained stable. These results demonstrate that climate change interacts with intraspecific variation through thermal tolerance, biomass advantages, and asymmetric gene flow to drive potential lineage replacement within the native range, a process already suggested by field observations of FEAU expansion in a plateau lake. Our findings argue for integrating evolutionary history and genetic identity into ecological forecasting to better anticipate ecosystem responses under ongoing warming.</description>
      <author>guowh@email.sdu.edu.cn (Cui Wang)</author>
      <author>guowh@email.sdu.edu.cn (Huijia Song)</author>
      <author>guowh@email.sdu.edu.cn (Lele Lin)</author>
      <author>guowh@email.sdu.edu.cn (Lele Liu)</author>
      <author>guowh@email.sdu.edu.cn (Weihua Guo)</author>
      <author>guowh@email.sdu.edu.cn (Wenyi Sheng)</author>
      <author>guowh@email.sdu.edu.cn (Yaolin Guo)</author>
      <author>guowh@email.sdu.edu.cn (Yuhui Wang)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.112160</guid>
      <category>Ecology</category>
      <category>Plant Biology</category>
      <pubDate>Mon, 21 Sep 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-09-21T00:00:00Z</dc:date>
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    </item>
    <item>
      <title>Environmental temperature is a strong driver of subspecies competition in the &lt;i&gt;Drosophila&lt;/i&gt; microbiome</title>
      <link>https://elifesciences.org/articles/110808</link>
      <description>Most microbiome research focuses on the taxonomic composition at the species level to understand the impact of environmental factors, but intraspecific diversity has largely been ignored. To address this significant knowledge gap, we took advantage of the simple, culturable microbiome of &lt;i&gt;Drosophila&lt;/i&gt;. First, we documented that natural populations of &lt;i&gt;D. simulans&lt;/i&gt; harbor three diverged clades of &lt;i&gt;Lactiplantibacillus plantarum&lt;/i&gt;, a key nutritional symbiont. We studied the distinct ecological roles of these three clades by exposing flies with their native microbiome to two temperature regimes in the laboratory. Tracking the three clades within the complete &lt;i&gt;Drosophila&lt;/i&gt; microbiome over a period of more than 10 years at two temperatures, we identified strikingly distinct dynamics in response to the selection regime. We confirmed the functional differentiation of the three clades using in vitro growth measurements and in vivo mono-association assays. Our results highlight that environmental selection operates at the subspecies level. Therefore, we conclude that the functional diversification of the microbiome can only be understood when intra- and interspecific diversity is considered.</description>
      <author>schlotc@gmail.com (Christian Schlötterer)</author>
      <author>schlotc@gmail.com (Juan Bosco Gracia Alvira)</author>
      <author>schlotc@gmail.com (Stefanie Migotti)</author>
      <author>schlotc@gmail.com (Viola Nolte)</author>
      <author>schlotc@gmail.com (Xiaomeng Tian)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110808</guid>
      <category>Ecology</category>
      <category>Microbiology and Infectious Disease</category>
      <pubDate>Fri, 18 Sep 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-09-18T00:00:00Z</dc:date>
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    </item>
    <item>
      <title>Small mammalian herbivores at moderate densities facilitate livestock growth by improving vegetation composition in grasslands</title>
      <link>https://elifesciences.org/articles/111340</link>
      <description>Small mammals and large herbivores have co-evolved in grasslands for millions of years, yet how they interact remains unclear. Although large herbivores can significantly affect the smaller ones, the reverse effect is largely unknown. On the Qinghai–Tibetan Plateau, plateau pikas (&lt;i&gt;Ochotona curzoniae&lt;/i&gt;) are often considered pests that compete with livestock at high densities. Using field experiments, we show that the presence of pikas facilitates weight gains of yaks (&lt;i&gt;Bos grunniens&lt;/i&gt;) by improving vegetation composition at a moderate density level. Compared to the pika-present treatment, pika removal dramatically increased cover of the poisonous &lt;i&gt;Stellera&lt;/i&gt; forbs by twofold, reducing the abundance and protein content of palatable grasses and sedges, yak foraging efficiency, and yak weight gain by up to 42%. Notably, we found a humped relationship between yak weight gains and pika burrow densities in the pika-present plots; the facilitative effect of pikas on yaks was highest at about 200 burrows/ha, but shifted to a competitive effect at pika densities exceeding 400 burrows/ha. These results provide the first empirical evidence that maintaining a moderate density of small mammalian herbivores can benefit growth performance of livestock by improving vegetation composition. Our study highlights the significance of moderate populations of ecosystem-engineering small mammals in sustaining pastoral productivity in rangelands.</description>
      <author>gaoy823@nenu.edu.cn (Bingbo Ni)</author>
      <author>gaoy823@nenu.edu.cn (Christopher R Dickman)</author>
      <author>gaoy823@nenu.edu.cn (Douglas Lawton)</author>
      <author>gaoy823@nenu.edu.cn (Fujiang Hou)</author>
      <author>gaoy823@nenu.edu.cn (Huakun Zhou)</author>
      <author>gaoy823@nenu.edu.cn (Jens-Christian Svenning)</author>
      <author>gaoy823@nenu.edu.cn (Junhu Su)</author>
      <author>gaoy823@nenu.edu.cn (Quanmin Dong)</author>
      <author>gaoy823@nenu.edu.cn (Shikui Dong)</author>
      <author>gaoy823@nenu.edu.cn (Wenjin Li)</author>
      <author>gaoy823@nenu.edu.cn (Xiaofei Li)</author>
      <author>gaoy823@nenu.edu.cn (Xiaona Zheng)</author>
      <author>gaoy823@nenu.edu.cn (Ying Gao)</author>
      <author>gaoy823@nenu.edu.cn (Zhenggang Guo)</author>
      <author>gaoy823@nenu.edu.cn (Zhibin Zhang)</author>
      <author>gaoy823@nenu.edu.cn (Zhiwei Zhong)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.111340</guid>
      <category>Ecology</category>
      <pubDate>Tue, 08 Sep 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-09-08T00:00:00Z</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>Stage-specific threats reveal the inadequacy of adult-centered conservation</title>
      <link>https://elifesciences.org/articles/110823</link>
      <description>In an era of severe global biodiversity threats, understanding the link between species’ traits and their endangerment helps uncover causes of risk and infer threats to understudied species. Most animals have complex life cycles with distinct stages that may face stage-specific threats. Current conservation frameworks rely heavily on adult traits, potentially misjudging extinction risk. Using Chinese anurans as a model, we integrated functional traits from both adult and tadpole stages to examine their association with extinction risk. We found that body size positively correlates with risk in both stages. Microhabitat use is related to extinction risk in tadpoles, but shows no significant link in adults. Adult relative tympanum diameter and head length also correlate with extinction risk. These results indicate that species vulnerability is correlated with multi-stage traits, with both shared and stage-specific threats. Conservation based solely on adult traits may fail to accurately assess species threats. We call for integrating a whole-life-history perspective into biodiversity assessment and conservation to more effectively address the global biodiversity crisis.</description>
      <author>doublelqq@163.com (Qing-Qing Li)</author>
      <author>doublelqq@163.com (Wei-Wei Zhou)</author>
      <author>doublelqq@163.com (Yan-Fang Song)</author>
      <author>doublelqq@163.com (Yong-Le Wang)</author>
      <author>doublelqq@163.com (Zhi-Yong Yuan)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110823</guid>
      <category>Ecology</category>
      <pubDate>Mon, 07 Sep 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-09-07T00:00:00Z</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>Soil extracellular DNA fragments show variable degradation rates among sequences and environmental conditions</title>
      <link>https://elifesciences.org/articles/110251</link>
      <description>While extracellular DNA (eDNA) persistence substantially influences soil microbiome investigations, its degradation kinetics remain poorly quantified. Here, we developed a primer-labeled DNA approach coupled with microcosm incubation to determine the overall and sequence-specific degradation rates of eDNA amplicon fragments across China. We observed substantial variations in the overall degradation rates of extracellular 16S rRNA gene amplicon fragments among the study sites, with degradation rate constants ranging from 0.05 to 0.16 day&lt;sup&gt;−1&lt;/sup&gt;. The overall degradation rate constants showed significant correlations with soil moisture content, prokaryotic abundance, prokaryotic community profiles, and mean annual precipitation. The significant influences of moisture content on the overall degradation rates were further verified by a moisture gradient microcosm experiment. The sequence-specific degradation rate constant profiles were additionally correlated with pH, nitrogen content, and mean annual temperature. Furthermore, propidium monoazide-based exclusion of eDNA signals significantly altered soil prokaryotic abundance, richness, and prokaryotic community profiles, and the pool sizes of sequence-specific extracellular 16S rRNA gene amplicon fragments were significantly correlated with their respective degradation rates. This study developed a methodology for determining the overall and sequence-specific degradation rates of eDNA amplicon fragments, highlighting the profound influences of eDNA on soil microbial research and informing the optimization of environmental DNA technologies.</description>
      <author>cherongxiao@ynu.edu.cn (Dong Liu)</author>
      <author>cherongxiao@ynu.edu.cn (Fang Wang)</author>
      <author>cherongxiao@ynu.edu.cn (Rongxiao Che)</author>
      <author>cherongxiao@ynu.edu.cn (Song Zhang)</author>
      <author>cherongxiao@ynu.edu.cn (Ting Li)</author>
      <author>cherongxiao@ynu.edu.cn (Wei Huang)</author>
      <author>cherongxiao@ynu.edu.cn (Xiaoyong Cui)</author>
      <author>cherongxiao@ynu.edu.cn (Zejin Zhang)</author>
      <author>cherongxiao@ynu.edu.cn (Zelin Wang)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110251</guid>
      <category>Ecology</category>
      <pubDate>Fri, 04 Sep 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-09-04T00:00:00Z</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>Evolution of sideways locomotion in crabs</title>
      <link>https://elifesciences.org/articles/110015</link>
      <description>The evolutionary change in the mode of locomotion is often a major evolutionary event, triggering diversification. Sideways locomotion is a defining feature of true crabs (Brachyura) and may have contributed to their ecological success. Yet, the evolutionary origin of this unique behavior remains unknown. Here, we show that the prevalence of sideways locomotion in true crabs reflects a single evolutionary origin from a forward-moving ancestor. Our behavioral analysis of 50 live crab species indicates that crab locomotion can be broadly separated into two predominant modes, sideways and forward locomotion. The phylogenetic comparative analysis revealed a single origin of sideways locomotion, with multiple independent reversions to forward locomotion in ecologically specialized groups. The species richness data show that the lineage in which sideways locomotion originated is far more diverse than its nearest outgroups. These results are consistent with the idea that sideways locomotion acted as a key innovation contributing to the evolutionary diversification of true crabs. Such a rare but innovative behavioral trait provides a framework for understanding how locomotor modes shape evolutionary diversification in animals.</description>
      <author>yuuki-k@nagasaki-u.ac.jp (Atsushi Hirai)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Fumio Takeshita)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Jung-Fu Huang)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Junya Taniguchi)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Kano Kohara)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Nobuaki Mizumoto)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Tsubasa Inoue)</author>
      <author>yuuki-k@nagasaki-u.ac.jp (Yuuki Kawabata)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110015</guid>
      <category>Ecology</category>
      <category>Evolutionary Biology</category>
      <pubDate>Thu, 27 Aug 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-08-27T00:00:00Z</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>Crickets evade bats via olfaction beyond acoustic cues</title>
      <link>https://elifesciences.org/articles/110936</link>
      <description>The evolutionary arms race between insectivorous bats and their insect prey is a classic paradigm of acoustic predation and evasion, with insects having evolved sophisticated auditory countermeasures. Both bats and insects also rely heavily on olfaction for key behaviors, such as social communication. Moreover, predator-derived odors are well established as risk cues in many other predator–prey systems. However, whether olfaction plays a role in the bat–insect arms race remains unknown. Here, we unveil a previously unknown olfactory dimension to this interaction. We demonstrated that the body odor of the insectivorous bat &lt;i&gt;Scotophilus kuhlii&lt;/i&gt; triggered robust avoidance and electrophysiological antennal responses in a common cricket prey, &lt;i&gt;Loxoblemmus equestris&lt;/i&gt;. We identified limonene as a behaviorally active volatile in bat odor that elicited electrophysiological responses in cricket antennae and was sufficient to elicit avoidance in crickets. Field experiments confirmed that limonene exposure reduced cricket calling activity, demonstrating the ecological relevance of this cue. Our findings establish that insects can detect and initiate avoidance of phylogenetically distant vertebrate predators via olfaction, a process that could be mediated by the elemental perception of individual odor compounds. This work broadens the sensory framework of a classic predator–prey system and highlights olfactory eavesdropping as a functional strategy in phylogenetically distant predator–prey systems.</description>
      <author>fengj@nenu.edu.cn (Aiqing Lin)</author>
      <author>fengj@nenu.edu.cn (Hanhong Xu)</author>
      <author>fengj@nenu.edu.cn (Jiang Feng)</author>
      <author>fengj@nenu.edu.cn (Jiaqi Wei)</author>
      <author>fengj@nenu.edu.cn (Wenhao Zhang)</author>
      <author>fengj@nenu.edu.cn (Yannan Li)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.110936</guid>
      <category>Ecology</category>
      <pubDate>Fri, 21 Aug 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-08-21T00:00:00Z</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>Global relationships between body size and urban affinity across more than 30,000 plant and animal species</title>
      <link>https://elifesciences.org/articles/109047</link>
      <description>Urbanization is a major global driver of biodiversity change, with species responses to urban settings ranging from avoidance to exploitation. To better understand these responses, we conducted a global analysis of urban relative affinity inferred from occurrence data across more than 30,000 animal and plant species. Our synthesis showed a consistent pattern across taxa and biogeographic regions: many species are urban avoiders, while few thrive as urban exploiters—a pattern we coin ‘species urbanness distribution’. We then assessed whether body size, an integrative ecological trait fundamental to space use, mobility, metabolism, and environmental sensitivity, showed consistent associations with urban affinity among species and across 371 taxonomic families. Analyses were conducted at the interspecific level and focused primarily on variation among taxonomic families (with an accompanying application to view results available for each family here: &lt;a href="https://globalecologyresearchgroup.github.io/Callaghan_et_al-2026-eLife-ShinyApp/"&gt;https://globalecologyresearchgroup.github.io/Callaghan_et_al-2026-eLife-ShinyApp/&lt;/a&gt;). Larger body sizes were generally associated with greater urban affinity in plants compared to animals, though these size-affinity relationships showed considerable variability among families. Our findings highlight the heterogeneous relationship between body size and urban affinity across the tree of life, underscoring the importance of tailored strategies to support urban biodiversity. This research advances ecological understanding of urban filtering and provides a framework for guiding biodiversity-sensitive urban planning amid accelerating global urbanization.</description>
      <author>c.callaghan@ufl.edu (Brittany M Mason)</author>
      <author>c.callaghan@ufl.edu (Corey T Callaghan)</author>
      <author>c.callaghan@ufl.edu (Diana E Bowler)</author>
      <author>c.callaghan@ufl.edu (Ingmar Staude)</author>
      <author>c.callaghan@ufl.edu (John H Wilshire)</author>
      <author>c.callaghan@ufl.edu (Laura H Antao)</author>
      <author>c.callaghan@ufl.edu (Thomas Merckx)</author>
      <author>c.callaghan@ufl.edu (Vaughn Shirey)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.109047</guid>
      <category>Ecology</category>
      <pubDate>Tue, 11 Aug 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-08-11T00:00:00Z</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>Correction: The neuropeptide sulfakinin is a peripheral regulator of insect behavioral switch between mating and foraging</title>
      <link>https://elifesciences.org/articles/112748</link>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.112748</guid>
      <category>Ecology</category>
      <pubDate>Tue, 28 Jul 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-07-28T00:00:00Z</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>Dopamine and its receptor &lt;i&gt;DcDop2&lt;/i&gt; are involved in the coevolution between ‘&lt;i&gt;Candidatus&lt;/i&gt; Liberibacter asiaticus’ and &lt;i&gt;Diaphorina citri&lt;/i&gt;</title>
      <link>https://elifesciences.org/articles/109081</link>
      <description>‘&lt;i&gt;Candidatus&lt;/i&gt; Liberibacter asiaticus’ (&lt;i&gt;C&lt;/i&gt;Las), the causal agent of citrus huanglongbing, is transmitted by the Asian citrus psyllid &lt;i&gt;Diaphorina citri&lt;/i&gt;. While &lt;i&gt;C&lt;/i&gt;Las-positive (&lt;i&gt;C&lt;/i&gt;Las+) females exhibit increased fecundity and metabolic demands, their neuroendocrine regulation mechanisms remain unclear. We propose &lt;i&gt;C&lt;/i&gt;Las manipulates dopamine (DA) signaling to enhance psyllid fecundity and &lt;i&gt;C&lt;/i&gt;Las proliferation. Metabolomics revealed elevated DA in &lt;i&gt;C&lt;/i&gt;Las+ females. Silencing DA synthesis genes and receptor &lt;i&gt;DcDop2&lt;/i&gt; via RNAi reduced lipid reserves, fecundity, and ovarian &lt;i&gt;C&lt;/i&gt;Las titers. Through combined &lt;i&gt;in vivo&lt;/i&gt; and &lt;i&gt;in vitro&lt;/i&gt; experiments, we demonstrated that the microRNA miR-31a suppresses &lt;i&gt;DcDop2&lt;/i&gt; expression by binding to its 3’ untranslated region. Overexpression of miR-31a resulted in decreased &lt;i&gt;DcDop2&lt;/i&gt; expression and &lt;i&gt;C&lt;/i&gt;Las titers in the ovaries, eliciting phenotypic defects akin to &lt;i&gt;DcDop2&lt;/i&gt; knockdown. Furthermore, &lt;i&gt;DcDop2&lt;/i&gt; knockdown and miR-31a overexpression reduced juvenile hormone (JH) levels and adipokinetic hormone (AKH) signaling in fat bodies and ovaries. Consequently, &lt;i&gt;C&lt;/i&gt;Las regulates the DA-&lt;i&gt;DcDop2&lt;/i&gt; signaling axis to improve &lt;i&gt;D. citri&lt;/i&gt; lipid metabolism and fecundity, while simultaneously promoting its replication. These findings reveal a coevolution between &lt;i&gt;C&lt;/i&gt;Las proliferation and ovarian development in the insect host. This discovery enhances our understanding of the molecular interplay between plant pathogens and vector insects and offers novel targets and strategies for HLB field management.</description>
      <author>zhangsongdou1128@126.com (George Andrew Charles Beattie)</author>
      <author>zhangsongdou1128@126.com (Jiayun Li)</author>
      <author>zhangsongdou1128@126.com (Jielan He)</author>
      <author>zhangsongdou1128@126.com (Jilei Huang)</author>
      <author>zhangsongdou1128@126.com (Paul Holford)</author>
      <author>zhangsongdou1128@126.com (Songdou Zhang)</author>
      <author>zhangsongdou1128@126.com (Weiwei Yuan)</author>
      <author>zhangsongdou1128@126.com (Xiaoge Nian)</author>
      <author>zhangsongdou1128@126.com (Yijing Cen)</author>
      <author>zhangsongdou1128@126.com (Yurong He)</author>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.109081</guid>
      <category>Ecology</category>
      <pubDate>Mon, 22 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-22T00:00:00Z</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>Retraction: Exogenous myristate fuels the growth of symbiotic arbuscular mycorrhizal fungi but disrupts their carbon-phosphorus exchange with host plants</title>
      <link>https://elifesciences.org/articles/112384</link>
      <guid isPermaLink="false">https://dx.doi.org/10.7554/eLife.112384</guid>
      <category>Ecology</category>
      <pubDate>Thu, 18 Jun 2026 00:00:00 +0000</pubDate>
      <dc:date>2026-06-18T00:00:00Z</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>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>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <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>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <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>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <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>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </item>
    <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>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </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>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </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>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>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>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>
      <webfeeds:featuredImage url="https://elife-cdn.s3.amazonaws.com/observer/elife-logo-408x230.svg" height="230" width="408" type="image/svg"/>
    </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"/>
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