Many authors have suggested that the negative effects of roads on animals are largely owing to traffic noise. Although suggestive, most past studies of the effects of road noise on wildlife were conducted in the presence of the other confounding effects of roads, such as visual disturbance, collisions and chemical pollution among others. We present, to our knowledge, the first study to experimentally apply traffic noise to a roadless area at a landscape scale-thus avoiding the other confounding aspects of roads present in past studies. We replicated the sound of a roadway at intervals-alternating 4 days of noise on with 4 days off-during the autumn migratory period using a 0.5 km array of speakers within an established stopover site in southern Idaho. We conducted daily bird surveys along our 'Phantom Road' and in a nearby control site. We document over a one-quarter decline in bird abundance and almost complete avoidance by some species between noise-on and noise-off periods along the phantom road and no such effects at control sites-suggesting that traffic noise is a major driver of effects of roads on populations of animals.
Decades of research demonstrate that roads impact wildlife and suggest traffic noise as a primary cause of population declines near roads. We created a "phantom road" using an array of speakers to apply traffic noise to a roadless landscape, directly testing the effect of noise alone on an entire songbird community during autumn migration. Thirty-one percent of the bird community avoided the phantom road. For individuals that stayed despite the noise, overall body condition decreased by a full SD and some species showed a change in ability to gain body condition when exposed to traffic noise during migratory stopover. We conducted complementary laboratory experiments that implicate foraging-vigilance behavior as one mechanism driving this pattern. Our results suggest that noise degrades habitat that is otherwise suitable, and that the presence of a species does not indicate the absence of an impact.traffic noise pollution | songbird migration | habitat degradation | foraging-vigilance trade-off | perceived predation risk H uman infrastructure shapes animal behaviors, distributions, and communities (1, 2). A meta-analysis of 49 datasets from across the globe found that bird populations decline within 1km of human infrastructure, including roads (2). Observational studies of birds near roads implicate traffic noise as a primary driver of these declines (3). Road ecology research has also shown negative correlations between traffic noise levels and songbird reproduction (4, 5). Birds that produce low frequency songs, likely masked by traffic noise, show the strongest avoidance of roads (6).There is now substantial evidence that anthropogenic noise has detrimental impacts on a variety of species (3, 7-10). For example, work in natural gas extraction fields has demonstrated that compressor station noise alters songbird breeding distribution and species richness (11-13). However, explicit experiments would help to further rule out other characteristics of infrastructure, such as visual disturbance, collisions, chemical pollution, and edge effects, which might be driving these patterns (3). In addition, although these studies implicate noise as a causal factor in population declines, many individuals remain despite noise exposure (3), but at what cost? Proposed causes of decreased fitness for birds in noise include song masking, interference with mate evaluation, nonrandom distribution of territorial individuals, disruption of parentchick communication, reduced foraging opportunities, and/or alterations in the foraging/vigilance trade-off (3, 4).Here we parse the independent role of traffic noise from other aspects of roads experimentally by playing traffic sounds in a roadless area, creating a 'phantom road'. We focus on birds during migratory stopover, because energy budgets are streamlined; foraging, vigilance, and rest dominate activity (14). To meet the amplified physiological needs of sustained nocturnal migratory flights, birds must increase foraging during periods of stopover while maintaining appropriate vigil...
Aim: Raptors serve critical ecological functions, are particularly extinction-prone and are often used as environmental indicators and flagship species. Yet, there is no global framework to prioritize research and conservation actions on them. We identify for the first time the factors driving extinction risk and scientific attention on raptors and develop a novel research and conservation priority index (RCPI) to identify global research and conservation priorities. Location: Global. Methods: We use random forest models based on ecological traits and extrinsic data to identify the drivers of risk and scientific attention in all raptors. We then map global research and conservation priorities. Lastly, we model where priorities fall relative to country-level human social indicators. Results: Raptors with small geographic ranges, scavengers, forest-dependent species and those with slow life histories are particularly extinction-prone. Research is extremely biased towards a small fraction of raptor species: 10 species (1.8% of all raptors) account for one-third of all research, while one-fifth of species have no publications. Species with small geographic ranges and those inhabiting less developed countries are greatly understudied. Regions of Latin America, Africa and Southeast Asia are identified as particularly high priority for raptor research and conservation. These priorities are highly concentrated in developing countries, indicating a global mismatch between priorities and capacity for research and conservation. Main conclusions: A redistribution of scientific attention and conservation efforts towards developing tropical countries and the least-studied, extinction-prone species is critical to conserve raptors and their ecological functions worldwide. We identify clear taxonomic and geographic research and conservation priorities for all raptors, and our methodology can be applied across other taxa to prioritize scientific investment. K E Y W O R D S avian biology, biogeography, conservation biology, conservation prioritization, ecology, extinction, ornithology, predator Editor: Diederik Strubbe | 857 BUECHLEY Et aL.
Adaptations to divert the attacks of visually guided predators have evolved repeatedly in animals. Using high-speed infrared videography, we show that luna moths (Actias luna) generate an acoustic diversion with spinning hindwing tails to deflect echolocating bat attacks away from their body and toward these nonessential appendages. We pit luna moths against big brown bats (Eptesicus fuscus) and demonstrate a survival advantage of ∼47% for moths with tails versus those that had their tails removed. The benefit of hindwing tails is equivalent to the advantage conferred to moths by bat-detecting ears. Moth tails lured bat attacks to these wing regions during 55% of interactions between bats and intact luna moths. We analyzed flight kinematics of moths with and without hindwing tails and suggest that tails have a minimal role in flight performance. Using a robust phylogeny, we find that long spatulate tails have independently evolved four times in saturniid moths, further supporting the selective advantage of this anti-bat strategy. Diversionary tactics are perhaps more common than appreciated in predator-prey interactions. Our finding suggests that focusing on the sensory ecologies of key predators will reveal such countermeasures in prey.antipredator defense | bat-moth interactions | Lepidoptera | Saturniidae P redators are under pressure to perform incapacitating initial strikes to thwart prey escape. It is thought that prey, in turn, have evolved conspicuous colors or markings to deflect predator attack to less vulnerable body regions (1, 2). Eyespots are a wellknown class of proposed deflection marks (3), which are found in a variety of taxa, including Lepidoptera (3) and fishes (4), but only recently have experiments convincingly demonstrated that these color patterns redirect predatory assault. Eyespots on artificial butterfly (5) and fish (4) prey draw strikes of avian and fish predators. Eyespots on the wing margins of woodland brown butterflies (Lopinga achine) lure the attacks of blue tits (Cyanistes caeruleus) (6). Brightly colored lizard tails also divert avian predator attacks to this expendable body region (7).Deflection coloration is unlikely to be an effective strategy against echolocating bats, as these predators have scotopic vision and poor visual acuity unsuited for prey localization and discrimination (8). Most bats rely on echoes from their sonar cries to image prey and other objects in their environment-they live in an auditory world (9). Thus, we would expect a deflection strategy, effective against bats, to present diversionary acoustic signatures to these hearing specialists. Weeks (10) proposed that saturniid hindwing tails might serve to divert bat attacks from essential body parts. We hypothesized that saturniid tails, spinning behind a flying moth (Movie S1) and reflecting sonar calls, serve as either a highly contrasting component of the primary echoic target or as an alternative target. We predicted that bats would aim their attacks at moth tails, instead of the wings or body, durin...
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