Annette Stange-Marten, Maximilian Greif, Steven Abendroth, Manuela Nowotny
{"title":"Neuronal processing of complex sounds in the prothoracic ganglion of a bushcricket.","authors":"Annette Stange-Marten, Maximilian Greif, Steven Abendroth, Manuela Nowotny","doi":"10.1007/s00359-026-01796-3","DOIUrl":"10.1007/s00359-026-01796-3","url":null,"abstract":"<p><p>Male bushcrickets produce complex species-specific songs to attract mating partners. Since the neuronal processing underlying song-pattern detection is not fully understood, we analysed extracellularly recorded song-induced spike responses and local field potentials across the first stage of auditory processing in the prothoracic ganglion of Mecopoda elongata. We analysed the influence of the temporal structure and of any change in amplitude of spiking and local field potentials. We presented the complete chirp and compared the neuronal response pattern with those responses evoked individually by each pulse of the chirp. Our data revealed: (i) the complete chirp leads to a transient summation in local field potentials over the time course of the chirp, and (ii) significantly fewer action potentials occur during the chirp presentation than to the individually presented pulses. Our data provide insights into the question of how an acoustical signal can be used to extract those features from sensory information that are important for auditory behaviour, such as chorus formation, species recognition, or phonotaxis.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"541-553"},"PeriodicalIF":2.3,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13198461/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147516803","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Anais Cotton, Christophe Barbraud, Sarah Leclaire, Karine Delord, Aymeric Bodin, Antoine Stier, Cécile Ribout, Charline Parenteau, Jean-Baptiste Ferdy, Charlotte Bourgoin, Joël White, Frédéric Angelier, Pierrick Blanchard
{"title":"Physiological and behavioural responses of wandering albatross chicks (Diomedea exulans) to novel and non-novel predators.","authors":"Anais Cotton, Christophe Barbraud, Sarah Leclaire, Karine Delord, Aymeric Bodin, Antoine Stier, Cécile Ribout, Charline Parenteau, Jean-Baptiste Ferdy, Charlotte Bourgoin, Joël White, Frédéric Angelier, Pierrick Blanchard","doi":"10.1007/s00359-026-01793-6","DOIUrl":"10.1007/s00359-026-01793-6","url":null,"abstract":"<p><p>In long-standing predator-prey systems, prey typically evolve costly responses to predation risk. How prey respond to novel predators is less investigated. We explored physiological (corticosterone, triglyceride), morphological (body condition) and behavioural (defensive posture) responses of wandering albatross (Diomedea exulans) chicks to a novel predator, the feral cat (Felis catus) in Kerguelen archipelago. We implemented a semi-experimental design to increase the variance in cat abundance by regulating cat populations in certain zones of the study colony. The aforementioned chick traits were then monitored and analysed at the zone scale, by comparing nests located within regulated and non-regulated zones, and at the nest scale, by recording cat abundance through intensive camera traps monitoring. This fine-scale approach further enabled us to investigate how chicks responded to southern giant petrels (Macronectes giganteus), an opportunistic predator-scavenger that has co-evolved with albatrosses. Cat abundances had no effect on chick traits. In contrast, higher abundances of giant petrel were associated with an elevated rate of corticosterone increase and lower triglyceride levels. In accordance with these results suggesting a more accurate perception of predation risk mediated by giant petrels than by cats, chicks were more prone to display a defensive posture when facing a giant petrel than a cat. We discuss these results in the light of contrasting evolutionary histories and predation patterns between albatrosses and their predators, and we emphasise that studies of predator impacts on prey populations must consider both the direct and indirect effects of all predators, as well as their interactions.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"501-514"},"PeriodicalIF":2.3,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13198508/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146087986","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Noah Packard, Jillian M Sills, Ryan A Jones, Seri T Aldana, Colleen Reichmuth
{"title":"Sensitivity to airborne sounds in ice-dependent bearded seals.","authors":"Noah Packard, Jillian M Sills, Ryan A Jones, Seri T Aldana, Colleen Reichmuth","doi":"10.1007/s00359-025-01782-1","DOIUrl":"10.1007/s00359-025-01782-1","url":null,"abstract":"<p><p>As the Arctic warms and becomes more accessible to human activities and associated noise sources, it is important to understand the auditory capabilities of ice-associated marine mammals that rely on sound. In this study, the in-air hearing of one adult bearded seal (Erignathus barbatus) was measured in ambient outdoor conditions using psychophysical methods. 50% detection thresholds were measured for 10 frequencies (0.04-51.2 kHz) that extend across the subject's hearing range. For low to mid frequencies (0.04-12.8 kHz), thresholds were constrained, or masked, by ambient noise. Thresholds obtained at higher frequencies (25.6-51.2 kHz) were sufficiently elevated above background noise to provide absolute measures of hearing sensitivity. These measurements reveal that the high-frequency roll-off for bearded seals is in alignment with available auditory data for related species despite more than 11 million years of evolutionary isolation. Further, the data collected at low and mid frequencies enable an unconventional estimation of critical ratios, which can be applied in masking models. Collectively, these findings for bearded seals listening for airborne sounds highlight auditory similarities within the northern clade of phocid Carnivores and improve predictions of potential noise effects for seals in changing Arctic soundscapes.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"465-472"},"PeriodicalIF":2.3,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13198493/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145679608","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Mechanosensory cephalic bristles mediate rapid flight initiation in hawkmoths.","authors":"Maitri Manjunath, Sanjay P Sane","doi":"10.1007/s00359-025-01762-5","DOIUrl":"10.1007/s00359-025-01762-5","url":null,"abstract":"<p><p>Endothermic insects including bees, butterflies, and moths need to warm up their flight muscles before taking flight. For instance, diurnal butterflies bask in the sun to heat their flight muscles, whereas nocturnal hawkmoths display a pre-flight shivering behavior in which small-amplitude wing movements cause flight muscles to warm up, eventually generating large-amplitude wing motion for flight. The time required for warm-up puts such insects at considerable risk if they need to rapidly escape from predators. Here, we show that upon experiencing a sudden air-puff on the head, hawkmoths with lower thoracic temperatures can rapidly initiate flight without the need for pre-flight shivering. This response is mediated by mechanosensory cephalic bristles that are located beneath the scales on their head. When activated, these bristles trigger a set of flight-related reflexes including antennal positioning, foreleg extension, wing movement, and abdominal flexion. Some of the mechanosensory neurons associated with the cephalic bristles arborize in the subesophageal zone (SEZ) and antennal motor and mechanonsensory centre (AMMC), whereas most arborize in pro-, meso- and meta-thoracic ganglia, which contain the motor circuitry for foreleg motion, flight, and abdominal flexion. Thermal recordings revealed that large-amplitude flapping following cephalic bristle-stimulation occurs at lower thoracic temperatures than required for endogenously-initiated take off. Electromyogram recordings from steering and indirect flight muscles show significant variability in activation latency in response to cephalic bristle stimuli. The range of latency values among different muscles overlaps, suggesting that cephalic bristle stimulation broadly activates indirect flight and steering muscles, thereby generating high-amplitude wing movement at lower thoracic temperatures. Thus, akin to locusts, the cephalic bristle system in hawkmoths rapidly triggers flight upon sensing danger, ensuring swift escape from potential threats.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"297-311"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13086664/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145423480","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Divergent sensory transcriptomic profiles in positive and negative learning in Bicyclus Anynana butterflies.","authors":"Yi Ting Ter, Erica L Westerman","doi":"10.1007/s00359-025-01771-4","DOIUrl":"10.1007/s00359-025-01771-4","url":null,"abstract":"<p><p>Mate preference learning, where individuals learn to prefer or avoid specific phenotypes during mate selection, is pervasive across animal taxa and influences reproductive isolation and trait evolution. Despite its significance, the genetic basis underlying the associated valence attribution (whether to prefer or avoid) remains largely unclear. Both in terms of what genes are associated with attributing valence, and whether valence attribution is associated with transcriptional changes in both sensory tissues and neural circuits in the brain, or is restricted to the brain. Here, we investigate the neurogenomic basis of positive and negative mate preference learning using Bicyclus anynana butterflies. We put females in positive or negative training scenarios, as well as a naïve control, and compared their transcriptomic profiles across three tissues: antennae, eyes, and brain using RNA-sequencing. Our results reveal tissue-specific transcriptional responses, with the antennae showing higher transcriptomic changes during negative training and the eyes showing higher transcriptomic changes during positive training, relative to the naïve control, indicating that valence attribution during learning may not be restricted to transcriptional changes in the brain. We identified a subset of genes in each tissue whose expression patterns changed with valence, as well as genes previously linked to classical conditioning pathways, supporting the hypothesis that imprinting-like learning and classical conditioning share molecular mechanisms. Our findings suggest that valence attribution in mate preference learning involves tissue-specific transcriptional responses in sensory and brain tissues, emphasising the role of peripheral sensory systems in modulating learned mate preferences.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"283-296"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13086741/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145350053","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Kristina Brauburger, Willi Ribi, Emelie Svensson, Paul Clémençon, Sho Yee Carisa Goh, Marjorie A Liénard, Eric Warrant, Stanley Heinze
{"title":"The visual system of a nocturnal long-distance migrant, the Australian Bogong moth.","authors":"Kristina Brauburger, Willi Ribi, Emelie Svensson, Paul Clémençon, Sho Yee Carisa Goh, Marjorie A Liénard, Eric Warrant, Stanley Heinze","doi":"10.1007/s00359-025-01786-x","DOIUrl":"10.1007/s00359-025-01786-x","url":null,"abstract":"<p><p>The Australian Bogong moth (Agrotis infusa) is a small noctuid moth that undertakes annual, nocturnal migrations of up to 1000 km to escape the summer heat of its breeding grounds. The moths travel to cool alpine caves, where they enter a dormant state (aestivation) before returning to reproduce and die. During migration, their brains integrate magnetic and visual cues to guide their flight direction. While the Bogong moth's neurobiology is increasingly understood, its visual system has remained unexplored. Here, we describe the morphology, ultrastructure, optics, and visual opsins of the Bogong moth's compound eyes and ocelli. Using light and electron microscopy, micro-computed tomography, in situ hybridization, and spectral absorbance measurements, we show that the compound eyes are typical superposition eyes with a tiered rhabdom, similar to other noctuid moths. The ocelli are small but structurally complex, featuring a two-tiered retina with spectrally distinct receptor cells and a lens forming a focused image on the ocellar retina. At the molecular level, the Bogong moth expresses three canonical opsins (UV, blue, and long-wavelength) and an additional red-shifted long-wavelength opsin, suggesting enhanced sensitivity to long-wavelength light. These opsins exhibit distinct expression patterns across the compound eyes, indicating functionally distinct dorsal and ventral eye hemispheres. Overall, the Bogong moth's visual system displays multiple adaptations to nocturnal vision. These features, likely shared across noctuid moths, may have contributed to the evolution of the exceptional navigational abilities during long-distance migrations in dim light that define the Bogong moth, but which are also widespread across noctuid moths.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"359-389"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13086690/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776385","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Sam J England, Callum F McLellan, Rochelle J Meah, J Benito Wainwright, Lauren Sumner-Rooney
{"title":"The sensory ecology of caterpillars.","authors":"Sam J England, Callum F McLellan, Rochelle J Meah, J Benito Wainwright, Lauren Sumner-Rooney","doi":"10.1007/s00359-025-01778-x","DOIUrl":"10.1007/s00359-025-01778-x","url":null,"abstract":"<p><p>Caterpillars (larval Lepidoptera) are one of the most ecologically and evolutionarily significant taxa on Earth. As both feeders and food, they shape the dynamics of enumerate ecosystems on land. Key to this prominent role in nature is the sensory systems that inform, guide, and trigger their behaviour. Gaining an understanding of caterpillar sensory ecology therefore promises to reveal fundamental insights into the broader principles of ecology and evolution, conservation and management, within and beyond the Lepidoptera. To facilitate such an understanding, here we review the existing literature on the sensory physiology and ecology of all currently recognised sensory modalities in caterpillars, namely vision, hearing, vibration detection, touch, electroreception, chemoreception, hygroreception, thermoreception, and graviception. In each of these sensory modalities, we also explore the current evidence surrounding the threat of anthropogenic sensory pollution. Taken together, this review reveals the great depth and breadth of research into caterpillar sensory ecology, making clear the value of caterpillars to neuroethology, but also of neuroethology to caterpillars. However, many of the attributes that caterpillars bring to neuroethological research are yet to be taken advantage of. For example, there is currently a lack of comparative sensory system studies on caterpillars, utilising their ecological diversity and existing phylogenetic data. We also highlight many considerable knowledge gaps, most pertinently, the need to identify the sensors responsible for each sensory modality in caterpillars, and to characterise the potential effects of sensory pollution across all of these modalities.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"153-178"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13086807/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145459998","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Correction: Cellular innovations and diversity in the lepidopteran compound eye.","authors":"Wei Lu, Marcus R Kronforst","doi":"10.1007/s00359-025-01758-1","DOIUrl":"10.1007/s00359-025-01758-1","url":null,"abstract":"","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"243-244"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13086765/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145514538","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Neuroethology on the move with butterflies and moths.","authors":"Anna Stöckl, Basil El Jundi, Kentaro Arikawa","doi":"10.1007/s00359-026-01798-1","DOIUrl":"10.1007/s00359-026-01798-1","url":null,"abstract":"<p><p>Lepidopteran insects, namely butterflies and moths, are visually striking and have fascinated scientists as well as the general public for decades, prompting fundamental questions about how they live and evolve. On the occasion of the International Congress of Neuroethology in Berlin in 2024, we had a satellite symposium entitled “Lepidopteran Neuroethology” for the first time, which motivated us to create this Special Issue of the Journal of Comparative Physiology A. This Special Issue highlights recent advances in sensory perception, flight control, navigation, neuroanatomy, and evolution through seven review articles and nine original research papers, together representing the breadth and richness of neuroethological research across Lepidoptera. The Issue concludes with an insightful review of emerging tools that are shaping future research in the field.</p>","PeriodicalId":54862,"journal":{"name":"Journal of Comparative Physiology A-Neuroethology Sensory Neural and Behavioral Physiology","volume":" ","pages":"147-151"},"PeriodicalIF":2.3,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147437669","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}