Regenerative abilities and their evolution in the different animal lineages have fascinated generations of biologists. While some taxa are capable of restoring entire individuals from small body fragments, others can regrow only specific structures or lack structural regeneration completely. In contrast to many other protostomes, including the segmented annelids, molting animals (Ecdysozoa) are commonly considered incapable of primary body axis regeneration, which has been hypothesized to be linked to the evolution of their protective cuticular exoskeleton. This holds also for the extraordinarily diverse, segmented arthropods. Contradicting this long-standing paradigm, we here show that immatures of the sea spider Pycnogonum litorale reestablish the posterior body pole after transverse amputation and can regrow almost complete segments and the terminal body region, including the hindgut, anus, and musculature. Depending on the amputation level, normal phenotypes or hypomeric six-legged forms develop. Remarkably, also the hypomeric animals regain reproductive functionality by ectopic formation of gonoducts and gonopores. The discovery of such complex regenerative patterns in an extant arthropod challenges the hitherto widely assumed evolutionary loss of axial regeneration during ecdysozoan evolution. Rather, the branching of sea spiders at the base of Chelicerata and their likely ancestral anamorphic development suggests that the arthropod stem species may have featured similar regenerative capabilities. Accordingly, our results provide an incentive for renewed comparative regeneration studies across ecdysozoans, with the aim to resolve whether this trait was potentially even inherited from the protostome ancestor.

Camera traps are an increasingly popular survey tool for ecological research and biodiversity conservation, but studies investigating their impact on focal individuals have been limited to only a few mammal species. In this context, echolocating bats are particularly interesting as they rely less on vision for navigation, yet show a strong negative reaction to constant illumination. At hibernacula, camera traps with white flash could offer an efficient alternative method for monitoring threatened bat species, but the potential negative impact of white flash on bat behavior is unknown. Here, we investigate the effect of camera traps emitting white flash at four hibernation sites fitted with infrared light barriers, infrared video cameras, and acoustic recorders over 16 weeks. At each site, the flash was turned off every second week. We quantified whether flash affected (1) nightly bat passes using generalized linear mixed models, (2) flight direction of entering bats using permutational multivariate analyses, and (3) latency of the first echolocation call after the camera trap trigger using randomization tests. Additionally, we quantified and corrected for the potential impact of confounding factors, such as weather and social interactions. Overall, white flash did not influence short‐ or long‐term bat activity, flight direction or echolocation behavior. A decrease in nightly bat activity was observed with an increasing proportion of hours with rain. Moreover, flight direction was affected by the presence of other bats, likely due to chasing and avoidance behavior. Our findings highlight the potential of camera traps with white flash triggered by infrared light barriers as a minimally invasive method for long‐term bat population monitoring and observation of species‐specific phenology. Such automated monitoring technologies can improve our understanding of long‐term population dynamics across a wide range of spatial‐temporal scales and taxa and consequently, contribute to data‐driven wildlife conservation and management.

Background Pycnogonida (sea spiders) is the sister group of all other extant chelicerates (spiders, scorpions and relatives) and thus represents an important taxon to inform early chelicerate evolution. Notably, phylogenetic analyses have challenged traditional hypotheses on the relationships of the major pycnogonid lineages (families), indicating external morphological traits previously used to deduce inter-familial affinities to be highly homoplastic. This erodes some of the support for phylogenetic information content in external morphology and calls for the study of additional data classes to test and underpin in-group relationships advocated in molecular analyses. In this regard, pycnogonid internal anatomy remains largely unexplored and taxon coverage in the studies available is limited. Results Based on micro-computed X-ray tomography and 3D reconstruction, we created a comprehensive atlas of in-situ representations of the central nervous system and midgut layout in all pycnogonid families. Beyond that, immunolabeling for tubulin and synapsin was used to reveal selected details of ganglionic architecture. The ventral nerve cord consistently features an array of separate ganglia, but some lineages exhibit extended composite ganglia, due to neuromere fusion. Further, inter-ganglionic distances and ganglion positions relative to segment borders vary, with an anterior shift in several families. Intersegmental nerves target longitudinal muscles and are lacking if the latter are reduced. Across families, the midgut displays linear leg diverticula. In Pycnogonidae, however, complex multi-branching diverticula occur, which may be evolutionarily correlated with a reduction of the heart. Conclusions Several gross neuroanatomical features are linked to external morphology, including intersegmental nerve reduction in concert with trunk segment fusion, or antero-posterior ganglion shifts in partial correlation to trunk elongation/compaction. Mapping on a recent phylogenomic phylogeny shows disjunct distributions of these traits. Other characters show no such dependency and help to underpin closer affinities in sub-branches of the pycnogonid tree, as exemplified by the tripartite subesophageal ganglion of Pycnogonidae and Rhynchothoracidae. Building on this gross anatomical atlas, future studies should now aim to leverage the full potential of neuroanatomy for phylogenetic interrogation by deciphering pycnogonid nervous system architecture in more detail, given that pioneering work on neuron subsets revealed complex character sets with unequivocal homologies across some families.