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The tremendous diversity of Hymenoptera is commonly attributed to the evolution of parasitoidism in the last common ancestor of parasitoid sawflies (Orussidae) and wasp-waisted Hymenoptera (Apocrita). However, Apocrita and Orussidae differ dramatically in their species richness, indicating that the diversification of Apocrita was promoted by additional traits. These traits have remained elusive due to a paucity of sawfly genome sequences, in particular those of parasitoid sawflies. Here, we present comparative analyses of draft genomes of the primarily phytophagous sawfly Athalia rosae and the parasitoid sawfly Orussus abietinus. Our analyses revealed that the ancestral hymenopteran genome exhibited traits that were previously considered unique to eusocial Apocrita (e.g., low transposable element content and activity) and a wider gene repertoire than previously thought (e.g., genes for CO2 detection). Moreover, we discovered that Apocrita evolved a significantly larger array of odorant receptors than sawflies, which could be relevant to the remarkable diversification of Apocrita by enabling efficient detection and reliable identification of hosts.

Based on a hybrid model of Europa's magnetospheric interaction, we provide context for the magnetic field perturbations observed by the Juno spacecraft during its only close flyby of the moon in September 2022. By systematically varying the incident flow conditions and the density profile of Europa's atmosphere, we demonstrate that the observed, large‐scale signatures of magnetic field draping are consistent with a dawn‐dusk asymmetry in the moon's neutral envelope. During the flyby, such an asymmetry would have enhanced the magnetic perturbations in Europa's anti‐Jovian hemisphere, explaining why the spacecraft already detected strong field line draping while still several moon radii away. Conversely, a reduced neutral density in the sub‐Jovian hemisphere can explain why the perturbations in the flow‐aligned field component remained nearly constant as Juno approached Europa. While a dawn‐dusk asymmetry in Europa's atmosphere has been predicted by theoretical work, our results provide the first in situ hints of its presence. Plain Language Summary: Located within Jupiter's magnetosphere, the small Galilean moon Europa is continuously exposed to a flow of magnetized plasma, traveling at a relative velocity of about 100 km/s. The deflection of this plasma around Europa generates perturbations to Jupiter's magnetic field, as observed for the first time in two decades during the flyby of the Juno spacecraft in 2022. The magnitude and extension of these magnetic perturbations are largely determined by the shape of Europa's atmosphere and ionosphere which represent obstacles to the incident magnetospheric plasma. To provide three‐dimensional context for the structure of Europa's magnetic environment at the time of the Juno flyby, we have applied a computer simulation to study the moon's interaction with the plasma flow. Comparison between modeled and observed magnetic fields suggests that, at the time when Juno collected these data, Europa's atmosphere may have been denser in the anti‐Jovian than in the Jupiter‐facing hemisphere. Theoretical predictions suggest such an asymmetry to be present in Europa's neutral envelope, partially generated by centrifugal and Coriolis forces acting on the gas molecules during the moon's rotation around Jupiter. Our study reveals first hints from a spacecraft flyby that such a hemispheric asymmetry may indeed exist in Europa's atmosphere. Key Points: By applying a hybrid model (kinetic ions, fluid electrons), we study Europa's interaction with Jupiter's magnetosphere during the Juno flybyA dawn‐dusk asymmetry in Europa's atmosphere can reproduce the large‐scale structure of the draping signatures seen by the Juno magnetometerThe spacecraft encountered the center of Europa's southern Alfven wing during ingress and the periphery of the northern wing during egress [ABSTRACT FROM AUTHOR]

Genetic disorders such as neurofibromatosis type 1 increase vulnerability to cognitive and behavioral disorders, such as autism spectrum disorder and attention-deficit/hyperactivity disorder. Neurofibromatosis type 1 results from loss-of-function mutations in the neurofibromin gene and subsequent reduction in the neurofibromin protein (Nf1). While the mechanisms have yet to be fully elucidated, loss of Nf1 may alter neuronal circuit activity leading to changes in behavior and susceptibility to cognitive and behavioral comorbidities. Here we show that mutations decreasing Nf1 expression alter motor behaviors, impacting the patterning, prioritization, and behavioral state dependence in a Drosophila model of neurofibromatosis type 1. Loss of Nf1 increases spontaneous grooming in a nonlinear spatial and temporal pattern, differentially increasing grooming of certain body parts, including the abdomen, head, and wings. This increase in grooming could be overridden by hunger in food-deprived foraging animals, demonstrating that the Nf1 effect is plastic and internal state-dependent. Stimulus-evoked grooming patterns were altered as well, with nf1 mutants exhibiting reductions in wing grooming when coated with dust, suggesting that hierarchical recruitment of grooming command circuits was altered. Yet loss of Nf1 in sensory neurons and/or grooming command neurons did not alter grooming frequency, suggesting that Nf1 affects grooming via higher-order circuit alterations. Changes in grooming coincided with alterations in walking. Flies lacking Nf1 walked with increased forward velocity on a spherical treadmill, yet there was no detectable change in leg kinematics or gait. Thus, loss of Nf1 alters motor function without affecting overall motor coordination, in contrast to other genetic disorders that impair coordination. Overall, these results demonstrate that loss of Nf1 alters the patterning and prioritization of repetitive behaviors, in a state-dependent manner, without affecting motor coordination., Competing Interests: Competing interest statement The authors declare no competing interests.

Among animals with visual processing mechanisms, the leech Hirudo verbana is a rare example in which all neurons can be identified. However, little is known about its visual system, which is composed of several pigmented head eyes and photosensitive non-pigmented sensilla that are distributed across its entire body. Although several interneurons are known to respond to visual stimuli, their response properties are poorly understood. Among these, the S-cell system is especially intriguing: it is multimodal, spans the entire body of the leech and is thought to be involved in sensory integration. To improve our understanding of the role of this system, we tested its spectral sensitivity, spatial integration and adaptation properties. The response of the S-cell system to visual stimuli was found to be strongly dependent on the size of the area stimulated, and adaptation was local. Furthermore, an adaptation experiment demonstrated that at least two color channels contributed to the response, and that their contribution was dependent on the adaptation to the background. The existence of at least two color channels was further supported by transcriptomic evidence, which indicated the existence of at least two distinct groups of putative opsins for leeches. Taken together, our results show that the S-cell system has response properties that could be involved in the processing of spatial and color information of visual stimuli. We propose the leech as a novel system to understand visual processing mechanisms with many practical advantages., Competing Interests: Competing interestsThe authors declare no competing or financial interests., (© 2019. Published by The Company of Biologists Ltd.)