Stressful environments have been suggested to enhance cooperative behaviours in animal communities. Prey animals living in risky environments can also increase long-term benefits by cooperating with neighbours, such as collectively harassing predators. However, empirical studies have rarely tested this prediction in the wild. In this experimental study we explored whether the perceived predation risk influences cooperative mobbing behaviour in tropical forest birds in French Guiana. The predation risk was increased by 5-d-long presentation of visual and acoustic stimuli of pygmy-owls in 24 locations. In order to examine whether mobbing response can vary in relation to the abundance of local predators, we used the Amazonian pygmy-owl (Glaucidium hardyi) as a common predator and the ferruginous pygmy-owl (Glaucidium brasilianum) as a rare predator in the study area. Our results showed that repeated predator-presentations increased mobbing response over time for the rarer owl species, while this effect was not significant for the common owl species. No effect of repeated presentations of either pygmy-owl species was found on the latency of mobbing. Moreover, mobbing latency was shorter and mobbing response was stronger for the common predator species, the Amazonian pygmy-owl. This study provides experimental evidence that birds exhibit stronger mobbing responses when the predator is locally abundant, while repeated encounters can be perceived as more dangerous when the predator is rare.

Studies in the Pacific have identified distinct killer whale ecotypes that are either specialized mammal- or fish-eaters. The different types have developed hunting strategies that would suggest specialization could be more advantageous than generalism. However, it has been suggested, based on long-term dietary markers of tooth wear and stable isotope values, that lineages in the North Atlantic are generalist, but with individual variation in the proportion of prey types consumed. Here, we present the results of ten years of observational and photo-identification data of a population of killer whales that follows the Norwegian spring-spawning stock of Atlantic herring. Although the whales were predominantly observed while feeding upon herring, one pod of herring-eating whales was also observed interacting with seals. This supports the hypothesis based on the long-term markers, of a degree of specialization, with a small number of groups persistently feeding upon mammals, but switching between herring and seals. We further investigated this prey switching by conducting playbacks of herring-eating killer whale sounds to harbour seals at haul-out sites on the herring spawning grounds. We recorded changes in behaviour consistent with an anti-predator response, suggesting the seals perceived the herring-eating killer whales as a potential predatory threat and had not habituated to their calls. This could be due to the risk of herring-eating killer whales switching to mammalian prey, or the difficulty of discriminating between killer whale pods due to the large population size and number of killer whale call dialects in this population, or a combination of both.

The neotropical terrestrial insectivore Henicorhina leucosticta (Troglodytidae) maintains long-term territories through vocalizations and forages among leaf litter trapped in the understorey vegetation and ground litter. The relationship between forest structure and H. leucosticta territory size was studied in La Selva Biological Station, Costa Rica, during the non-breeding season in 2009. Forest structure was measured by assessing canopy openness and leaf area index (LAI) using hemispherical photography, while territory size was estimated with the playback technique using local conspecific vocalizations. Mean territory area was 3.8 ± 2.8 ha (mean ± SD, n = 10). Territory radius length was similar in old-growth forest and abandoned agro-forest plantations. We found that H. leucosticta territory size decreased as median LAI increased. We propose that LAI is related to territory size through the amount of leaf fall and subsequent leaf litter accumulation over the understorey plants, which constitutes an important reservoir of arthropod prey and nest materials for H. leucosticta. The long-term supply of food resources is likely to affect territory size in this species, as well as other insectivorous birds with similar foraging behaviour. These results are congruent with the structural cues hypothesis.

The blue petrel (Halobaena caerulea) is a small pelagic seabird breeding on just a few Southern Ocean islands. Although it is known that oceanographic and climatic variability affect mortality rates, individual body condition and reproductive success, very few data are available on the global population status. We assessed the status of blue petrels at Mayes Island, Iles Kerguelen, in 2002 by estimating burrow densities and burrow occupancy using acoustic playbacks and response probability. The mean and highest burrow densities recorded were respectively 0.136 ± 0.026 and 2.3 entrances per m2. Burrow occupancy increased with burrow density but stabilized at c. 0.6 occupied burrows per m2. Taking into account the response probability to playback (0.819) the mean burrow occupancy density was 0.037 ± 0.094 per m2, giving an estimated 142 000 (95% CI around 106 000–179 000) or 148 000 breeding pairs (95% CI around 55 000–241 000) on Mayes Island, respectively with and without taking into account spatial autocorrelation in burrow densities. This suggests that the entire breeding population of blue petrels at Kerguelen is much higher than current estimates, and that Kerguelen and Diego Ramírez archipelagos are key breeding sites for this species.

Studies of mixed-species bird flocks have found that ‘nuclear’ species, those important to flock coherence, are either intraspecifically gregarious or are ‘sentinel’ species highly sensitive to predators. Both types of species are present in flocks of a Sri Lankan rain forest: orange-billed babblers (Turdoides rufescens Blyth) are highly gregarious, whereas greater racket-tailed drongos (Dicrurus paradiseus Linnaeus) are less so, but more sensitive and reliable alarm-callers. We hypothesized that flock participants would be attracted to the playback of both species more than to the clearly non-nuclear yellow-fronted barbet (Megalaima flavifrons Cuvier). Further, we hypothesized that insectivores would prefer babbler vocalizations, as babblers could facilitate their foraging in several ways. We found that the response of insectivores was three times greater during babbler or drongo playback, and eight times greater during playback of these two species together, than during barbet playback or silence. Insectivores did not show, however, any difference in their response to babbler as compared to drongo playback; omnivores and frugivores responded relatively equally to all treatments. Our results show that birds with high propensity to flock, such as insectivores, use the vocalizations of nuclear species to locate flocks and that a sentinel species may be as attractive as a highly gregarious species.

This paper describes a new vision-based playback method of a wheeled mobile robot. The path of the robot is divided into straight line parts and curved line parts. The curved line parts were approximated by a Bézier curve to decrease the volume of data. In order to track the curved line parts with good accuracy, tracking errors were detected by referring to two pre-recorded images on one part of the curve. Then, the errors were corrected by adjusting the control points of the Bézier curve. Outdoor experiments demonstrated good repeatability by using the proposed method.

The use of video images in place of natural stimuli in animal behaviour experiments is reviewed. Unlike most other artificial means of stimulus presentation, video stimuli can depict complex moving objects such as other animals, preserving the temporal and spatial patterns of movement precisely as well as colour and sounds for repeated playback. Computer editing can give flexibility and control over all elements of the stimulus. A variety of limitations of video image presentation are also considered. Televisions and video monitors are designed with human vision in mind, and some non-human animals that differ in aspects of visual processing such as their colour vision, critical flicker-fusion threshold, perception of depth and visual acuity, may perceive video images differently to ourselves. The failure of video stimuli to interact with subjects can be a drawback for some studies. For video to be useful, it is important to confirm that the subject animal responds to the image in a comparable way to the real stimulus, and the criteria used to assess this are discussed. Finally, the contribution made by video studies to date in the understanding of animal visual responses is considered, and recommendations as to the future uses of video are made.