Artificial light at night drives diel activity patterns of synanthropic pipistrelle bats and their prey.

The use of artificial light at night (ALAN) has increased drastically worldwide over the last decades. ALAN can have major effects on nocturnal communities, including insects and bats. Insects are attracted to street lights and few bat species take advantage of this by foraging on the attracted insects. ALAN potentially affects the temporal patterns of insect abundance and thereby bat foraging behaviour. In a natural dark environment, these patterns are usually bimodal, with an activity peak in the early evening and the morning. Little is known about how ALAN affects insect presence throughout the night, and whether the light spectrum plays a role. This is important, as these temporal changes may be a key driver of disturbances in bat-insect interactions. Here, we studied how white and red light affect insects' and bats' nightly activity patterns. The activity of insects and bats (Pipistrellus spp.) was recorded throughout the night at seven experimentally illuminated sites in a forest-edge ecosystem. ALAN disrupted activity patterns, with both insects and bats being more active throughout the night. ALAN facilitated all-night foraging in bats especially near white light, but these effects were attenuated near red light. The ability to forage throughout the night may be a key advantage causing synanthropic bats to dominate in illuminated environments, but this could also prove detrimental in the long term. As red light reduced disturbing effects of ALAN on insects and bats diel activity pattern, it opens the possibility of using spectral composition as a mitigation measure.

Combining acoustic tracking and LiDAR to study bat flight behaviour in three-dimensional space.

BACKGROUND: Habitat structure strongly influences niche differentiation, facilitates predator avoidance, and drives species-specific foraging strategies of bats. Vegetation structure is also a strong driver of echolocation call characteristics. The fine-scale assessment of how bats utilise such structures in their natural habitat is instrumental in understanding how habitat composition shapes flight- and acoustic behaviour. However, it is notoriously difficult to study their species-habitat relationship in situ. METHODS: Here, we describe a methodology combining Light Detection and Ranging (LiDAR) to characterise three-dimensional vegetation structure and acoustic tracking to map bat behaviour. This makes it possible to study fine-scale use of habitat by bats, which is essential to understand spatial niche segregation in bats. Bats were acoustically tracked with microphone arrays and bat calls were classified to bat guild using automated identification. We did this in multiple LiDAR scanned vegetation plots in forest edge habitat. The datasets were spatially aligned to calculate the distance between bats' positions and vegetation structures. RESULTS: Our results are a proof of concept of combining LiDAR with acoustic tracking. Although it entails challenges with combining mass-volumes of fine-scale bat movements and vegetation information, we show the feasibility and potential of combining those two methods through two case studies. The first one shows stereotyped flight patterns of pipistrelles around tree trunks, while the second one presents the distance that bats keep to the vegetation in the presence of artificial light. CONCLUSION: By combining bat guild specific spatial behaviour with precise information on vegetation structure, the bat guild specific response to habitat characteristics can be studied in great detail. This opens up the possibility to address yet unanswered questions on bat behaviour, such as niche segregation or response to abiotic factors in interaction with natural vegetation. This combination of techniques can also pave the way for other applications linking movement patterns of other vocalizing animals and 3D space reconstruction.

Luminescence control of Stomiidae photophores.

Nervous control of light emission from deep-sea mesopelagic fishes has been documented for several species. Studies on the nervous control of photophores from deep-sea luminescent fish, are mainly restricted to a pharmacological approach. For example, the light organs, called photophores, isolated from Argyropelecus hemygimnus and Maurolicus muelleri show a much higher sensitivity to adrenaline than to noradrenaline. According to these results and other information in different species, catecholamines are considered as main neurotransmitters triggering bioluminescence in deep-sea fishes. The present work is a study of the nervous control of the isolated photophores from two Stomiid fishes, Chauliodus sloani (the viperfish) and Stomias boa (the dragonfish) with the aim to determine the nature of the nervous control by pharmacological, biochemical and morphological approaches. Results show that, although the photophores of both species are sensitive to catecholamines, adrenaline is present in larger amount than noradrenaline in the light organs of C. sloani. Both catecholamines have different immunoreactive (IR) sites, noradrenaline showing a very diffuse localization as compared to adrenaline in C. sloani. On the contrary, only adrenaline is detected in the photocytes chamber and nerves innervating the photophore in S. boa. Knowing that the majority of dragonfishes exhibit a luminescent chin barbel, we also investigated the presence of catecholamines in this specific tissue in S. boa. Immunohistology reveals the presence of adrenaline within the tissue forming the chin barbel; adrenaline-IR is found in the connective tissue surroundings two group of muscle fibers and blood vessels in the stem but also around the multiple blood vessels located within the barbel bulb. Our results strongly support the adrenergic control of light emission in bioluminescent stomiid fishes.