Effects of traffic-regulated street lighting on nocturnal insect abundance and bat activity

New technological developments modulate the light levels of LED street luminaires according to traffic volumes: light levels are increased given traffic and reduced in its absence. Such dimming of street lights reduces the level of artificial light at night (ALAN) and may thus contribute to mitigate light pollution. To quantify the impact of traffic-driven dimming of street lights on nocturnal insect abundance and bat activity in comparison to full light (i.e., dimming functions of luminaires switched off), we mounted 20 insect flight-interception traps and ten batloggers on street light poles along two dimmable street light sections. Insect abundance and bat activity were measured alternately with one week of full street lighting followed by a week with light levels modulated by traffic volumes. In total, 16 dimmed and 16 full-light days were investigated. Overall, traffic-driven dimming reduced light levels by 35%. Weather conditions (warm, dry nights) were the main drivers of insect abundance and bat activity, but traffic-driven dimming resulted in lower numbers of insects caught and reduced bat activity. Among insect groups, Heteroptera benefited most from dimming. For bats, urban exploiters (Pipistrellus spp.) benefited from increased availability of prey at brightly lit street lights, while less frequent species (Myotis spp.) did not benefit from street lighting. We conclude that street light dimming technology may contribute to mitigate negative effects of ALAN on nocturnal organisms, although the measure may not be efficient enough to support light-sensitive and threatened species.     

Is part‐night lighting an effective measure to limit the impacts of artificial lighting on bats?

As light pollution is currently considered to be a major threat to biodiversity, different lighting management options are being explored to mitigate the impact of artificial lighting on wildlife. Although part‐night lighting schemes have been adopted by many local authorities across Europe to reduce the carbon footprint and save energy, their effects on biodiversity are unknown. Through a paired, in situ experiment, we compared the activity levels of 8 bat species under unlit, part‐night, and full‐night lighting treatments in a rural area located 60 km south of Paris, France. We selected 36 study locations composed of 1 lit site and a paired unlit control site; 24 of these sites were located in areas subject to part‐night lighting schemes, and 12 sites were in areas under standard, full‐night lighting. There was significantly more activity on part‐night lighting sites compared to full‐night lighting sites for the late‐emerging, light‐sensitive Plecotus spp., and a similar pattern was observable for Myotis spp., although not significant. In contrast, part‐night lighting did not influence the activity of early emerging bat species around streetlights, except for Pipistrellus pipistrellus for which there was significantly less activity on part‐night lighting sites than on full‐night lighting sites. Overall, no significant difference in activity between part‐ and full‐night lighting sites were observed in 5 of the 8 species studied, suggesting that current part‐night lighting schemes fail to encompass the range of activity of most bat species. We recommend that such schemes start earlier at night to effectively mitigate the adverse effects of artificial lighting on light‐sensitive species, particularly along ecological corridors that are especially important to the persistence of biodiversity in urban landscapes.     

Barriers and benefits: implications of artificial night-lighting for the distribution of common bats in Britain and Ireland

Artificial lighting is a particular problem for animals active at night. Approximately 69% of mammal species are nocturnal, and one-third of these are bats. Due to their extensive movements—both on a nightly basis to exploit ephemeral food supplies, and during migration between roosts—bats have an unusually high probability of encountering artificial light in the landscape. This paper reviews the impacts of lighting on bats and their prey, exploring the direct and indirect consequences of lighting intensity and spectral composition. In addition, new data from large-scale surveys involving more than 265 000 bat calls at more than 600 locations in two countries are presented, showing that prevalent street-lighting types are not generally linked with increased activity of common and widespread bat species. Such bats, which are important to ecosystem function, are generally considered ‘light-attracted’ and likely to benefit from the insect congregations that form at lights. Leisler''s bat (Nyctalus leisleri) may be an exception, being more frequent in lit than dark transects. For common pipistrelle bats (Pipistrellus pipistrellus), lighting is negatively associated with their distribution on a landscape scale, but there may be local increases in habitats with good tree cover. Research is now needed on the impacts of sky glow and glare for bat navigation, and to explore the implications of lighting for habitat matrix permeability.     

Pollination by nocturnal Lepidoptera,and the effects of light pollution: a review

1. Moths (Lepidoptera) are the major nocturnal pollinators of flowers. However, their importance and contribution to the provision of pollination ecosystem services may have been under‐appreciated. Evidence was identified that moths are important pollinators of a diverse range of plant species in diverse ecosystems across the world. 2. Moth populations are known to be undergoing significant declines in several European countries. Among the potential drivers of this decline is increasing light pollution. The known and possible effects of artificial night lighting upon moths were reviewed, and suggest how artificial night lighting might in turn affect the provision of pollination by moths. The need for studies of the effects of artificial night lighting upon whole communities of moths was highlighted. 3. An ecological network approach is one valuable method to consider the effects of artificial night lighting upon the provision of pollination by moths, as it provides useful insights into ecosystem functioning and stability, and may help elucidate the indirect effects of artificial light upon communities of moths and the plants they pollinate. 4. It was concluded that nocturnal pollination is an ecosystem process that may potentially be disrupted by increasing light pollution, although the nature of this disruption remains to be tested.     

Response of bats and nocturnal insects to urban green areas in Europe

Animal biodiversity in cities is generally expected to be uniformly reduced, but recent studies show that this is modulated by the composition and configuration of Urban Green Areas (UGAs). UGAs represent a heterogeneous network of vegetated spaces in urban settings that have repeatedly shown to support a significant part of native diurnal animal biodiversity. However, nocturnal taxa have so far been understudied, constraining our understanding of the role of UGAs on maintaining ecological connectivity and enhancing overall biodiversity. We present a well-replicated multi-city study on the factors driving bat and nocturnal insect biodiversity in three European cities. To achieve this, we sampled bats with ultrasound recorders and flying insects with light traps during the summer of 2018. Results showed a greater abundance and diversity of bats and nocturnal insects in the city of Zurich, followed by Antwerp and Paris. We identified artificial lighting in the UGA to lower bat diversity by probably filtering out light-sensitive species. We also found a negative correlation between both bat activity and diversity and insect abundance, suggesting a top-down control. An in-depth analysis of the Zurich data revealed divergent responses of the nocturnal fauna to landscape variables, while pointing out a bottom-up control of insect diversity on bats. Thus, to effectively preserve biodiversity in urban environments, UGAs management decisions should take into account the combined ecological needs of bats and nocturnal insects and consider the specific spatial topology of UGAs in each city.     

Urban bat communities are affected by wetland size,quality, and pollution levels

Wetlands support unique biota and provide important ecosystem services. These services are highly threatened due to the rate of loss and relative rarity of wetlands in most landscapes, an issue that is exacerbated in highly modified urban environments. Despite this, critical ecological knowledge is currently lacking for many wetland‐dependent taxa, such as insectivorous bats, which can persist in urban areas if their habitats are managed appropriately. Here, we use a novel paired landscape approach to investigate the role of wetlands in urban bat conservation and examine local and landscape factors driving bat species richness and activity. We acoustically monitored bat activity at 58 urban wetlands and 35 nonwetland sites (ecologically similar sites without free‐standing water) in the greater Melbourne area, southeastern Australia. We analyzed bat species richness and activity patterns using generalized linear mixed‐effects models. We found that the presence of water in urban Melbourne was an important driver of bat species richness and activity at a landscape scale. Increasing distance to bushland and increasing levels of heavy metal pollution within the waterbody also negatively influenced bat richness and individual species activity. Areas with high levels of artificial night light had reduced bat species richness, and reduced activity for all species except those adapted to urban areas, such as the White‐striped free‐tailed bat (Austronomus australis). Increased surrounding tree cover and wetland size had a positive effect on bat species richness. Our findings indicate that wetlands form critical habitats for insectivorous bats in urban environments. Large, unlit, and unpolluted wetlands flanked by high tree cover in close proximity to bushland contribute most to the richness of the bat community. Our findings clarify the role of wetlands for insectivorous bats in urban areas and will also allow for the preservation, construction, and management of wetlands that maximize conservation outcomes for urban bats and possibly other wetland‐dependent and nocturnal fauna.     

Light Pollution Modifies the Expression of Daily Rhythms and Behavior Patterns in a Nocturnal Primate

Among anthropogenic pressures, light pollution altering light/dark cycles and changing the nocturnal component of the environment constitutes a threat for biodiversity. Light pollution is widely spread across the world and continuously growing. However, despite the efforts realized to describe and understand the effects of artificial lighting on fauna, few studies have documented its consequences on biological rhythms, behavioral and physiological functions in nocturnal mammals. To determine the impacts of light pollution on nocturnal mammals an experimental study was conducted on a nocturnal primate, the grey mouse lemur Microcebus murinus. Male mouse lemurs (N = 8) were exposed 14 nights to moonlight treatment and then exposed 14 nights to light pollution treatment. For both treatments, chronobiological parameters related to locomotor activity and core temperature were recorded using telemetric transmitters. In addition, at the end of each treatment, the 14^th night, nocturnal and feeding behaviors were explored using an infrared camera. Finally, throughout the study, body mass and daily caloric food intake were recorded. For the first time in a nocturnal primate, light pollution was demonstrated to modify daily rhythms of locomotor activity and core temperature especially through phase delays and increases in core temperature. Moreover, nocturnal activity and feeding behaviors patterns were modified negatively. This study suggests that light pollution induces daily desynchronization of biological rhythms and could lead to seasonal desynchronization with potential deleterious consequences for animals in terms of adaptation and anticipation of environmental changes.     

Turning to the dark side: LED light at night alters the activity and species composition of a foraging bat assemblage in the northeastern United States

Artificial light at night (ALAN) is a rapidly intensifying form of environmental degradation that can impact wildlife by altering light‐mediated physiological processes that control a broad range of behaviors. Although nocturnal animals are most vulnerable, ALAN''s effects on North American bats have been surprisingly understudied. Most of what is known is based on decades‐old observations of bats around street lights with traditional lighting technologies that have been increasingly replaced by energy‐efficient broad‐spectrum lighting, rendering our understanding of the contemporary effects of ALAN on North American bats even less complete. We experimentally tested the effects of broad‐spectrum ALAN on presence/absence, foraging activity, and species composition in a Connecticut, USA bat community by illuminating foraging habitat with light‐emitting diode (LED) floodlights and comparing acoustic recordings between light and dark conditions. Lighting dramatically decreased presence and activity of little brown bats (Myotis lucifugus), which we detected on only 14% of light nights compared with 65% of dark (lights off) and 69% of control (lights removed) nights. Big brown bat (Eptesicus fuscus) activity on light nights averaged only half that of dark and control nights. Lighting did not affect presence/absence of silver‐haired bats (Lasionycteris noctivagans), but decreased their activity. There were no effects on eastern red bats (Lasiurus borealis) or hoary bats (L. cinereus), which have been described previously as light‐tolerant. Aversion to lighting by some species but not others caused a significant shift in community composition, thereby potentially altering competitive balances from natural conditions. Our results demonstrate that only a small degree of ALAN can represent a significant form of habitat degradation for some North American bats, including the endangered little brown bat. Research on the extent to which different lighting technologies, colors, and intensities affect these species is urgently needed and should be a priority in conservation planning for North America''s bats.     

The Switch from Low-Pressure Sodium to Light Emitting Diodes Does Not Affect Bat Activity at Street Lights

We used a before-after-control-impact paired design to examine the effects of a switch from low-pressure sodium (LPS) to light emitting diode (LED) street lights on bat activity at twelve sites across southern England. LED lights produce broad spectrum ‘white’ light compared to LPS street lights that emit narrow spectrum, orange light. These spectral differences could influence the abundance of insects at street lights and thereby the activity of the bats that prey on them. Most of the bats flying around the LPS lights were aerial-hawking species, and the species composition of bats remained the same after the switch-over to LED. We found that the switch-over from LPS to LED street lights did not affect the activity (number of bat passes), or the proportion of passes containing feeding buzzes, of those bat species typically found in close proximity to street lights in suburban environments in Britain. This is encouraging from a conservation perspective as many existing street lights are being, or have been, switched to LED before the ecological consequences have been assessed. However, lighting of all spectra studied to date generally has a negative impact on several slow-flying bat species, and LED lights are rarely frequented by these ‘light-intolerant’ bat species.     

Artificial night lighting disrupts sex pheromone in a noctuid moth

1. One major, yet poorly studied, change in the environment is the increase in nocturnal light pollution. Although this strongly alters the habitat of nocturnal species, the ecological consequences are poorly known. Moths are well known to be attracted to artificial light sources, but artificial light may affect them in other ways as well. 2. In this study, female Mamestra brassicae moths were subjected to various types of low‐intensity artificial night lighting with contrasting spectral compositions (green‐rich, red‐rich, warm white) or to a dark control treatment and the effects on their sex pheromone production and composition were tested. 3. Artificial night lighting reduced sex pheromone production and altered the chemical composition of the pheromone blend, irrespective of spectral composition. Specifically, amounts of the main pheromone component Z11‐16:Ac were reduced, while the deterring compounds Z9‐14:Ac, Z9‐16:Ac, and Z11‐16:OH were increased relative to Z11‐16:Ac when females were kept under artificial light. These changes may reduce the effectiveness of the sex pheromones, becoming less attractive for males. 4. These results show for the first time that artificial light at night affects processes that are involved in moth reproduction. The potential for mitigation through manipulation of the spectral composition of artificial light appears limited.     

The dark side of street lighting: impacts on moths and evidence for the disruption of nocturnal pollen transport

Among drivers of environmental change, artificial light at night is relatively poorly understood, yet is increasing on a global scale. The community‐level effects of existing street lights on moths and their biotic interactions have not previously been studied. Using a combination of sampling methods at matched‐pairs of lit and unlit sites, we found significant effects of street lighting: moth abundance at ground level was halved at lit sites, species richness was >25% lower, and flight activity at the level of the light was 70% greater. Furthermore, we found that 23% of moths carried pollen of at least 28 plant species and that there was a consequent overall reduction in pollen transport at lit sites. These findings support the disruptive impact of lights on moth activity, which is one proposed mechanism driving moth declines, and suggest that street lighting potentially impacts upon pollination by nocturnal invertebrates. We highlight the importance of considering both direct and cascading impacts of artificial light.     

Light pollution alters the phenology of dawn and dusk singing in common European songbirds

Artificial night lighting is expanding globally, but its ecological consequences remain little understood. Animals often use changes in day length as a cue to time seasonal behaviour. Artificial night lighting may influence the perception of day length, and may thus affect both circadian and circannual rhythms. Over a 3.5 month period, from winter to breeding, we recorded daily singing activity of six common songbird species in 12 woodland sites, half of which were affected by street lighting. We previously reported on analyses suggesting that artificial night lighting affects the daily timing of singing in five species. The main aim of this study was to investigate whether the presence of artificial night lighting is also associated with the seasonal occurrence of dawn and dusk singing. We found that in four species dawn and dusk singing developed earlier in the year at sites exposed to light pollution. We also examined the effects of weather conditions and found that rain and low temperatures negatively affected the occurrence of dawn and dusk singing. Our results support the hypothesis that artificial night lighting alters natural seasonal rhythms, independently of other effects of urbanization. The fitness consequences of the observed changes in seasonal timing of behaviour remain unknown.     

Effects of experimental night lighting on the daily timing of winter foraging in common European songbirds

The ecological effects of light pollution are becoming better understood, especially in birds. Recent studies have shown that several bird species can use street lighting to extend activity into the night during the breeding season. However, most of these studies are correlational and little is known about the effects of artificial night lighting on the timing of activities outside the breeding season. During winter, low temperatures and short days may limit foraging opportunities and can negatively affect survival of resident birds. However, night lighting may allow them to expand the time niche available for foraging. Here, we report on a study where we repeatedly manipulated the amount of night lighting during early winter at automated feeding stations in a natural forest. We used video‐recordings at the feeders to determine the time of the first (at dawn) and last (at dusk) foraging visits for six songbird species. We predicted that all species, and in particular the naturally early‐foraging species, would advance their daily onset of foraging during the mornings with night lighting, but would show minimal or no delays in their daily cessation of foraging during the lighted evenings. We found that two early‐foraging species, the blue tit and the great tit, started foraging earlier during the experimentally lighted mornings. However, in great tits, this effect was weak and restricted to nights with inclement weather. The light treatment did not have any effect on the start of foraging in the willow/marsh tit, the nuthatch, the European jay, and the blackbird. Artificial night lighting did not cause later foraging at dusk in any of the six species. Overall, our results suggest that artificial light during winter has only small effects on timing of foraging. We discuss these findings and the importance of temperature and winter weather in shaping the observed foraging patterns.     

Tent-roosting may have driven the evolution of yellow skin coloration in Stenodermatinae bats

The recent discovery of the first mammal that deposits significant amounts of carotenoid pigments in the skin (the Honduran white bat Ectophylla alba) has highlighted the presence of conspicuous yellow coloration in the bare skin of some bats. This is patent in the subfamily Stenodermatinae, where many species build tents with plant leaves for communal roosting at daytime. On the basis that tents offer rich light conditions by partly allowing sunlight to pass through the leaves and this makes that yellow coloration probably provides camouflage benefits to tent-roosting bats, that gregariousness facilitates visual communication, and that all Stenodermatinae bats possess retinal L-cones that allow the perception of long-wavelength light and have a frugivorous diet from which carotenoids are obtained, we hypothesized that tent-roosting may have driven the evolution of yellow skin coloration in this group of bats. We tested this prediction in 71 species within Stenodermatinae. Reconstructions of ancestral states showed that the common ancestor was most likely not colorful and did not roost in tents, but both traits early appeared in the first phylogenetic ramification. Phylogenetically controlled analyses showed that, as predicted, yellow skin coloration and tent-roosting coevolved after their appearance. This is the first explanation for the evolution of body coloration in nocturnal mammals. As the light environment of nocturnal forests is dominated by yellow-green wavelengths that coincide with the spectral sensitivity of some bats, nocturnal light conditions may have acted jointly with diurnal light conditions in tents to favor the evolution of yellow skin coloration in these animals.     

Artificial light at night causes diapause inhibition and sex‐specific life history changes in a moth

Rapidly increasing levels of light pollution subject nocturnal organisms to major alterations of their habitat, the ecological consequences of which are largely unknown. Moths are well‐known to be attracted to light at night, but effects of light on other aspects of moth ecology, such as larval development and life‐history, remain unknown. Such effects may have important consequences for fitness and thus for moth population sizes. To study the effects of artificial night lighting on development and life‐history of moths, we experimentally subjected Mamestra brassicae (Noctuidae) caterpillars to low intensity green, white, red or no artificial light at night and determined their growth rate, maximum caterpillar mass, age at pupation, pupal mass and pupation duration. We found sex‐specific effects of artificial light on caterpillar life‐history, with male caterpillars subjected to green and white light reaching a lower maximum mass, pupating earlier and obtaining a lower pupal mass than male caterpillars under red light or in darkness. These effects can have major implications for fitness, but were absent in female caterpillars. Moreover, by the time that the first adult moth from the dark control treatment emerged from its pupa (after 110 days), about 85% of the moths that were under green light and 83% of the moths that were under white light had already emerged. These differences in pupation duration occurred in both sexes and were highly significant, and likely result from diapause inhibition by artificial night lighting. We conclude that low levels of nocturnal illumination can disrupt life‐histories in moths and inhibit the initiation of pupal diapause. This may result in reduced fitness and increased mortality. The application of red light, instead of white or green light, might be an appropriate measure to mitigate negative artificial light effects on moth life history.     

Public street lights increase house infestation by the Chagas disease vector Triatoma dimidiata

Triatoma dimidiata is one of the primary vectors of Chagas disease. We previously documented the spatio-temporal infestation of houses by this species in the Yucatan peninsula, Mexico, and found that non-domiciliated triatomines were specifically attracted to houses. However, the factors mediating this attraction remained unclear. Artificial light has been known for a long time to attract many insect species, and therefore may contribute to the spread of different vector-borne diseases. Also, based on the collection of different species of triatomines with light traps, several authors have suggested that light might attract triatomines to houses, but the role of artificial light in house infestation has never been clearly demonstrated and quantified. Here we performed a spatial analysis of house infestation pattern by T. dimidiata in relation to the distribution of artificial light sources in three different villages from the Yucatan peninsula, Mexico. In all three villages, infested houses were significantly closer to public street light sources than non-infested houses (18.0 ± 0.6 vs 22.6 ± 0.4 m), and street lights rather than domestic lights were associated with house infestation. Accordingly, houses closer to a public street lights were 1.64 times more likely to be infested than houses further away (OR, CI95% 1.23-2.18). Behavioral experiments using a dual-choice chamber further confirmed that adult male and females were attracted to white light during their nocturnal activity. Attraction was also dependent on light color and decreased with increasing wavelength. While public lighting is usually associated with increased development, these data clearly show that it also directly contributes to house infestation by non-domiciliated T. dimidiata.     

The effects of feedback lighting on the circadian drinking rhythm in the diurnal new world primate Saimiri sciureus

Feedback lighting provides illumination primarily during the subjective night (i.e., the photosensitive portion of the circadian cycle) in response to a given behavior. This technique has previously been used to test the nonparametric model of entrainment in nocturnal rodents. In three species (Rattus norvegicus, Mesocricetus auratus, and Mus musculus), the free-running period of the locomotor activity rhythm was similar whether the animals were exposed to continuous light or discrete light pulses occurring essentially only during the subjective night (i.e., feedback lighting). In the current experiments, feedback lighting was presented to squirrel monkeys so that light fell predominantly during the subjective night. Feedback lighting was linked to the drinking behavior in this diurnal primate so that when the animal drank, the lights went out. Despite the seemingly adverse predicament, the monkeys maintained regular circadian drinking rhythms. Furthermore, just as the period of the free-running activity rhythms of nocturnal rodents exposed to continuous light or feedback lighting were similar, the period of the drinking rhythms of the squirrel monkeys in continuous light and feedback lighting were comparable (25.6 +/- 0.1 and 25.9 +/- 0.1 hours, respectively), despite a substantial decrease in the total amount of light exposure associated with feedback lighting. The free-running period of monkeys exposed to continuous dark (24.5 +/- 0.1 hours) was significantly shorter than either of the two lighting conditions (P < 0.001). The results presented for the drinking rhythm were confirmed by examination of the temperature and activity rhythms. Therefore, discrete light pulses given predominately during the subjective night are capable of simulating the effects of continuous light on the free-running period of the circadian rhythms of a diurnal primate. The response of squirrel monkeys to feedback lighting thus lends further support for the model and suggests that the major entrainment mechanisms are similar in nocturnal rodents and diurnal primates.     

Light pollution is associated with earlier tree budburst across the United Kingdom

The ecological impact of night-time lighting is of concern because of its well-demonstrated effects on animal behaviour. However, the potential of light pollution to change plant phenology and its corresponding knock-on effects on associated herbivores are less clear. Here, we test if artificial lighting can advance the timing of budburst in trees. We took a UK-wide 13 year dataset of spatially referenced budburst data from four deciduous tree species and matched it with both satellite imagery of night-time lighting and average spring temperature. We find that budburst occurs up to 7.5 days earlier in brighter areas, with the relationship being more pronounced for later-budding species. Excluding large urban areas from the analysis showed an even more pronounced advance of budburst, confirming that the urban ‘heat-island’ effect is not the sole cause of earlier urban budburst. Similarly, the advance in budburst across all sites is too large to be explained by increases in temperature alone. This dramatic advance of budburst illustrates the need for further experimental investigation into the impact of artificial night-time lighting on plant phenology and subsequent species interactions. As light pollution is a growing global phenomenon, the findings of this study are likely to be applicable to a wide range of species interactions across the world.     

Contrasting effects of street light shapes and LED color temperatures on nocturnal insects and bats

Street lights are important light sources that contribute to artificial light at night (ALAN). To date, ecological impacts of individual LED properties (color temperature, dimmability) have been studied, while interactions between light properties or aspects of luminaire design have not been addressed. However, the design of luminaires can influence ALAN impacts as the shape determines the spatial distribution of light and its visibility in the environment. This may cause amplifying or mitigating effects. We assessed the relative individual and interacting effects of two LED luminaire designs and three LED color temperatures (1750 K, 3000 K, 4000 K) on nocturnal insect abundance, bat foraging and feeding activity. We considered a standard LED luminaire shape with focused light emission and a luminaire shape with a diffusor to scatter the light spatially, leading to increased visibility of the light in the environment. During 104 nights, we trapped 51263 nocturnal insects of which 97% were caught at lights and 3% at dark sites. For bats, up to 44.8% fewer acoustic signals were recorded at dark sites. We caught 31% insects at LEDs with1750 K, 34% and 35% at 3000 K and 4000 K, respectively. Thus, color temperatures of 1750 K proved less detrimental than 3000/4000 K. Effects of luminaire shape led to an increase (16%) of trapped insects for luminaires with diffusors compared to the standard shape. In addition, luminaires with diffusors amplified the effects of LED color (+12% insects at 1750 K/3000 K; +25.6% at 4000 K). In contrast, bat foraging activity was independent of the light treatments while bat feeding activity was increased by 21.5% at standard luminaire shapes. Likely, intense straylight at diffused lights negatively affects the target-focused echolocation by deterring the bats. We concluded that ecological impacts of luminaire shape are an important, yet underestimated variable in light-pollution impact research.     

Use of Forest Edges by Bats in a Managed Pine Forest Landscape

ABSTRACT Forest edges often have increased species richness and abundance (edge effect) and affect spatial behaviors of species and dynamics of species interactions. Landscapes of intensively managed pine (Pinus spp.) stands are characterized by a mosaic of patches and linear forest edges. Managed pine forests are a primary landscape feature of the southeastern United States, but the effects of intensive management on bat communities are poorly understood. Insectivorous bats are important top predators in nocturnal forest food webs. We examined bat foraging behavior along forest edges and in 4 structurally distinct stand types (open-canopy pine, prethinned pine, thinned pine, and unmanaged forest) within a managed pine forest in the coastal plain of North Carolina, USA. During May-August, 2006 and 2007, we recorded echolocation calls using Pettersson D240X bat detectors linked to digital recorders at 156 sites. We also sampled nocturnal flying insects at each site using Malaise insect traps. We used negative binomial count regression models to describe bat foraging behavior relative to forest edges, stand types, and prey availability. Although some species showed affinities for certain stand types and prey items, bat activity patterns were most strongly related to forest edges. Edges were used extensively by 6 aerial-hunting bat species, but avoided by Myotis species. Forest edges function similarly to natural forest gaps, by providing foraging opportunities for aerial-hunting bat species. Therefore, the maintenance of forest edges in managed pine landscapes may enhance foraging habitat for aerial-hunting bat species.