For many decades, the spectral composition of lighting was determined by the type of lamp, which also influenced potential effects of outdoor lights on species and ecosystems. Light-emitting diode (LED) lamps have dramatically increased the range of spectral profiles of light that is economically viable for outdoor lighting. Because of the array of choices, it is necessary to develop methods to predict the effects of different spectral profiles without conducting field studies, especially because older lighting systems are being replaced rapidly. We describe an approach to predict responses of exemplar organisms and groups to lamps of different spectral output by calculating an index based on action spectra from behavioral or visual characteristics of organisms and lamp spectral irradiance. We calculate relative response indices for a range of lamp types and light sources and develop an index that identifies lamps that minimize predicted effects as measured by ecological, physiological, and astronomical indices. Using these assessment metrics, filtered yellow-green and amber LEDs are predicted to have lower effects on wildlife than high pressure sodium lamps, while blue-rich lighting (e.g., K ≥ 2200) would have greater effects. The approach can be updated with new information about behavioral or visual responses of organisms and used to test new lighting products based on spectrum. Together with control of intensity, direction, and duration, the approach can be used to predict and then minimize the adverse effects of lighting and can be tailored to individual species or taxonomic groups.
Light pollution is increasing around the world and altering natural nightscapes with potential ecological and evolutionary consequences. A severe ecological perturbation caused by artificial lights is mass mortalities of organisms, including seabird fledglings that are attracted to lights at night on their first flights to the sea. Here, we report on the number of fledging short-tailed shearwaters Ardenna tenuirostris found grounded in evening and morning rescue patrols conducted at Phillip Island, Australia, during a 15-year period (1999–2013). We assessed factors affecting numbers of grounded birds and mortality including date, moon phase, wind direction and speed, number of visitors and holiday periods. We also tested experimentally if birds were attracted to lights by turning the lights off on a section of the road. Of 8871 fledglings found, 39% were dead or dying. This mortality rate was 4–8 times higher than reported elsewhere for other shearwater species, probably because searching for fledglings was part of our systematic rescue effort rather than the opportunistic rescue used elsewhere. Thus, it suggests that light-induced mortality of seabirds is usually underestimated. We rescued more birds (dead and alive) in peak fledging, moonless and windy nights. Mortality increased through the fledging period, in the mornings and with increased traffic on holiday periods. Turning the road lights off decreased the number of grounded birds (dead and alive). While moon, wind and time are uncontrolled natural constraints, we demonstrated that reduction of light pollution and better traffic management can mitigate artificial light-induced mortality.
Pathogen diversity is thought to drive major histocompatibility complex (MHC) polymorphism given that host's immune repertories are dependent on antigen recognition capabilities. Here, we surveyed an extensive community of pathogens (n = 35 taxa) and MHC diversity in mainland versus island subspecies of the Eurasian kestrel Falco tinnunculus and in a sympatric mainland population of the phylogenetically related lesser kestrel Falco naumanni. Insular subspecies are commonly exposed to impoverished pathogen communities whilst different species' ecologies and contrasting life-history traits may lead to different levels of pathogen exposure. Although specific host traits may explain differential particular infections, overall pathogen diversity, richness and prevalence were higher in the truly cosmopolitan, euriphagous and long-distance disperser Eurasian kestrel than in the estenophagous, steppe-specialist, philopatric but long-distance migratory lesser kestrel. Accordingly, the continental population of Eurasian kestrels displayed a higher number (64 vs. 49) as well as more divergent alleles at both MHC class I and class II loci. Detailed analyses of amino acid diversity revealed that significant differences between both species were exclusive to those functionally important codons comprising the antigen binding sites. The lowest pathogen burdens and the smallest but still quite divergent set of MHC alleles (n = 16) were found in island Eurasian kestrels, where the rates of allele fixation at MHC loci seem to have occurred faster than at neutral markers. The results presented in this study would therefore support the role of pathogen diversity and abundance in shaping patterns of genetic variation at evolutionary relevant MHC genes.
The use of artificial light at night and its ecological consequences are increasing around the world. Light pollution can lead to massive mortality episodes for nocturnally active petrels, one of the most threatened avian groups. Some fledglings can be attracted or disoriented by artificial light on their first flights. Studies testing the effect of artificial light characteristics on attractiveness to seabirds have not provided conclusive results and there is some urgency as some endangered petrel species experience high lightinduced mortality. We designed a field experiment to test the effect of three common outdoor lighting systems with different light spectra (high pressure sodium, metal halide and light emitting diode) on the number and the body condition of grounded fledglings of the short-tailed shearwater Ardenna tenuirostris. A total of 235 birds were grounded during 99 experimental hours (33 hours for each treatment). 47% of birds were grounded when metal halide lights were on, while light emitting diode and high pressure sodium lights showed lower percentages of attraction (29% and 24%). Metal halide multiplied the mortality risk by a factor of 1.6 and 1.9 respectively in comparison with light emitting diode and high pressure sodium lights. No differences in body condition were detected among the birds grounded by the different lighting systems. We recommend the adoption of high pressure sodium lights into petrel-friendly lighting designs together with other light mitigation measures such as light attenuation, lateral shielding to reduce spill and appropriate orientation.
Aim To identify the wintering grounds of the threatened western European Lesser Kestrels to focus conservation efforts in those areas.Location Huelva Province, southern Spain, as breeding range, and western Africa (Senegal and Mauritania), as wintering range. Methods We used archival light level geolocators (1.5 g) to map the wintering areas and determine some characteristics of the migratory journeys of 20 adult Lesser Kestrels from the Iberian Peninsula tagged in 2007.Results Thirteen geolocators were recovered the following breeding season (2008) after attachment in 2007. Four recovered geolocators provided useful data. According to kernel density analyses, kestrels wintered near the Senegal River (border between Mauritania and Senegal). Pre-nuptial migration took longer than the post-nuptial migration, which may be the consequence of a loop migration.Main conclusions Geolocators have solved a crucial conservation question (i.e. the winter destination of western European Lesser kestrels), and these devices have thus proved useful to determine the location of the winter quarters of small sized migratory species. Our data indicate that European Lesser Kestrels winter in West Africa, in accordance with previous suggestions based on scattered observations during the winter months. This valuable information should serve to focus conservation efforts both in northern Senegal and southern Mauritania. Large roosts gathering thousands of lesser kestrels had been recorded in these areas over the years, but there was no previous confirmation of individuals staying all winter long. Specific and sustained protection of the roost sites, where the birds may be most vulnerable, should be sought in conjunction with local authorities.
Colour polymorphism results from the expression of multiallelic genes generating phenotypes with very distinctive colourations. Most colour polymorphisms are due to differences in the type or amount of melanins present in each morph, which also differ in several behavioural, morphometric and physiological attributes. Melanin-based colour morphs could also differ in the levels of glutathione (GSH), a key intracellular antioxidant, because of the role of this molecule in melanogenesis. As GSH inhibits the synthesis of eumelanin (i.e. the darkest melanin form), individuals of darker morphs are expected to have lower GSH levels than those of lighter morphs. We tested this prediction in nestlings of two polymorphic raptors, the booted eagle Hieraaetus pennatus and the Eleonora's falcon Falco eleonorae, both of which occur in two morphs differing in the extent of eumelanic plumage. As expected, melanic booted eagle nestlings had lower blood GSH levels than light morph eagle nestlings. In the Eleonora's falcon, however, melanic nestlings only had lower GSH levels after controlling for the levels of other antioxidants. We also found that melanic female eagle nestlings had higher levels of antioxidants other than GSH and were in better body condition than light female eagle nestlings. These findings suggest an adaptive response of melanic nestlings to compensate for reduced GSH levels. Nevertheless, these associations were not found in falcons, indicating species-specific particularities in antioxidant machinery. Our results are consistent with previous work revealing the importance of GSH on the expression of melanic characters that show continuous variation, and suggest that this pathway also applies to discrete colour morphs. We suggest that the need to maintain low GSH levels for eumelanogenesis in dark morph individuals may represent a physiological constraint that helps regulate the evolution and maintenance of polymorphisms.
Light level geolocators, also known as GLS loggers, are electronic devices intended for tracking the location of wide‐ranging animals using ambient light to estimate latitude and longitude. Miniaturized geolocators that can be used on relatively small migratory birds have recently become available, but little is known about the potential harmful effects of geolocators on birds. We examined the possible effects of 1.5‐g geolocators (dimensions: 21 × 6.5 × 9 mm) on the breeding success and survival of migratory Lesser Kestrels (Falco naumanni). During the 2007 breeding season, kestrels were fitted with geolocators using two attachment methods (Teflon wing harnesses and darvic bands), and geolocators were removed in 2008 after the birds returned to the breeding grounds. We found no differences in the breeding success of control and tagged pairs during the 2007 breeding season, but tagged pairs had greater fledgling mortality in the following breeding season. Furthermore, nestlings of tagged individuals had higher triglyceride and uric acid concentrations in their blood than control nestlings during the breeding season following tagging. As for return rates, 75% of tagged birds came back to the colony after the nonbreeding period, a proportion similar to that reported in previous studies. Although back‐mounts are slightly heavier and require more skill to attach, we recommend their use on small migratory raptors because most leg‐mounted geolocators in this study were damaged or rendered useless by dirt obscuring the light sensor.
One of the most critical phases in the life of petrels (Procellariiformes) is at fledging when young birds pass from parental dependence on land to an independent life at sea. To mitigate mortality at this time, rescue programs are implemented near breeding sites around the world, especially for birds grounded by artificial lights. We evaluated the plumage and body condition of short‐tailed shearwater (Ardenna tenuirostris) fledglings captured at colonies just before departure in comparison to fledglings washed up on beaches and to fledglings attracted by artificial light along roads. We measured abundance of down, body mass, and body condition index as the standardized residuals of a regression of body mass on size, and employed linear models to test differences on body mass and body condition between locations. Beach‐washed birds were underweight and in poor condition, suggesting their future survival probabilities at sea were low. Birds rescued on roads as a consequence of light attraction had lower body weights and condition indices than fledglings captured at the colony. However, more than 50% of light‐attracted birds had attained similar weights to those of adults, suggesting they have higher probabilities of survival than beach‐washed birds. Water‐logged birds being washed onto beaches is a natural process, but birds grounded by lighting along roads is an increasing anthropogenic threat that requires management. Thus, management and conservation efforts should be directed to protect birds in the colonies and reduce light‐induced mortality, ideally through the strategic reduction of light sources and lateral light spillage. When resources for conservation are limited, rescue programs should focus on rescuing birds from roads rather than beach‐washed birds, which have a lower probability of survival. © 2017 The Wildlife Society.
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