While many acute and often fatal effects of direct light on nocturnal organisms are identified (Rich and Longcore 2006; Hölker et al. 2010a; Gaston et al. 2013), very little is known about what effect, if any, the diffuse light surrounding urban areas has on biodiversity. Because skyglow alters even nightscapes located far from urban areas, small behavioral responses to skyglow could produce significant changes in species distributions.
Many behavioral activities are synchronized with lunar cycles. In celestially lit environments, some organisms take advantage of moonless or cloudy nights to avoid predation during orientation, foraging, metamorphosis, and mating, or to synchronize reproduction with relation to the moon phase (Clarke 1983; Gliwicz 1986; Kronfeld-Schor et al. 2013). The addition of artificial skyglow can extinguish such lunar light cycles and permanently remove dark nights from a landscape (Davies et al. 2013; Puschnig et al. 2013). As a result, in one species of zooplankton (Daphnia retrocurva), skyglow was found to reduce the amplitude of diel vertical migration below the limits of experimental sensitivity (Moore et al. 2000).
Recently, Dacke et al. (2013) showed that dung beetles (Scarabaeus satyrus) use the diffuse band of light produced by the Milky Way on clear moonless nights as an orientation marker. Although Dacke et al. (2013) did not discuss it, their results imply these beetles lose much of their ability to orient, and suffer reduced fitness in areas affected by skyglow. Since there is no reason to believe that Milky Way navigation is restricted to Scarabaeus satyrus, we wonder whether skyglow is selecting against this remarkable trait worldwide, with possible consequences for biodiversity and ecosystem services? It was recently reported that dung beetle diversity is reduced with increasing urbanization (Korasaki et al. 2013). This loss is of special relevance for perturbed agro-ecosystems, since species-rich dung beetle communities are able to buffer ecosystem services such as dung decomposition and nutrient cycling (Beynon et al. 2012). Perhaps related studies focusing on nocturnal communities could test whether skyglow is indeed a selective pressure.
Reviews of studies on the effects of light at night have argued convincingly that skyglow must surely affect food webs and biodiversity, but no studies to date have demonstrated this. Navara and Nelson (2007) provide an excellent review of the effects of light on behavior and physiology, but changes due to skyglow are inferred based primarily on observed response to natural light levels (twilight or moonlight) or simulated studies in enclosures. Two such examples presented by Longcore and Rich (2004) are the dependence of coyote calling on moon phase, and the luminance range under which treefrogs are willing to forage. Longcore and Rich (2004) also discussed an unpublished result in which frogs halted mating during periods when a nearby stadium was lit. While these studies demonstrate or strongly imply that behavior is likely to change under conditions of skyglow, they don’t prove that skyglow has affected biodiversity in nocturnal landscapes.