ABSTRACT
As of yet there is no literature record of the hearing range of the Eurasian otter (Lutra lutra, L. 1758), a key species for natural conservation efforts in Europe. We recorded in-air pure tone hearing thresholds of anaesthetized otters using auditory brainstem responses (ABR) and report the results of the Eurasian otter. The recorded potentials showed the typical mammalian auditory brainstem response consisting of 5 distinct positive peaks during the first 10â¯ms after stimulus onset. At 80â¯dB SPL the hearing ranged from around 200â¯Hz to 32â¯kHz, with lowest thresholds around 4â¯kHz.
Subject(s)
Auditory Pathways/physiology , Auditory Threshold , Brain Stem/physiology , Evoked Potentials, Auditory, Brain Stem , Otters/physiology , Acoustic Stimulation , Animals , Audiometry, Pure-Tone , Female , Otters/psychology , Time FactorsABSTRACT
Cooperative problem solving has gained a lot of attention over the past two decades, but the range of species studied is still small. This limits the possibility of understanding the evolution of the socio-cognitive underpinnings of cooperation. Lutrinae show significant variations in socio-ecology, but their cognitive abilities are not well studied. In the first experimental study of otter social cognition, we presented two species-giant otters and Asian small-clawed otters-with a cooperative problem-solving task. The loose string task requires two individuals to simultaneously pull on either end of a rope in order to access food. This task has been used with a larger number of species (for the most part primates and birds) and thus allows for wider cross-species comparison. We found no differences in performance between species. Both giant otters and Asian small-clawed otters were able to solve the task successfully when the coordination requirements were minimal. However, when the temporal coordination demands were increased, performance decreased either due to a lack of understanding of the role of a partner or due to difficulty inhibiting action. In conclusion, two species of otters show some ability to cooperate, quite similar to most other species presented with the same task. However, to draw further conclusions and more nuanced comparisons between the two otter species, further studies with varied methodologies will be necessary.
Subject(s)
Otters/psychology , Problem Solving , Social Behavior , Animals , Cognition , Female , MaleABSTRACT
This focus article was prepared by Paul Duff, Paul Holmes and Alex Barlow of the APHA Wildlife Expert Group.
Subject(s)
Animal Diseases/epidemiology , Animals, Wild , Sentinel Surveillance/veterinary , Animals , Animals, Wild/virology , Anura , Bird Diseases/epidemiology , Bird Diseases/virology , Birds , Deer/virology , Influenza in Birds/epidemiology , Male , Malignant Catarrh/epidemiology , Orthomyxoviridae Infections/epidemiology , Orthomyxoviridae Infections/veterinary , Otters/psychology , Predatory Behavior , Seals, Earless/virology , United Kingdom/epidemiologyABSTRACT
According to the "social intelligence hypothesis," species with complex social interactions have more sophisticated communication systems. Giant otters (Pteronura brasiliensis) live in groups with complex social interactions. It is likely that the vocal communication of giant otters is more sophisticated than previous studies suggest. The objectives of the current study were to describe the airborne vocal repertoire of giant otters in the Pantanal area of Brazil, to analyze call types within different behavioral contexts, and to correlate vocal complexity with level of sociability of mustelids to verify whether or not the result supports the social intelligence hypothesis. The behavior of nine giant otters groups was observed. Vocalizations recorded were acoustically and statistically analyzed to describe the species' repertoire. The repertoire was comprised by 15 sound types emitted in different behavioral contexts. The main behavioral contexts of each sound type were significantly associated with the acoustic variable ordination of different sound types. A strong correlation between vocal complexity and sociability was found for different species, suggesting that the communication systems observed in the family mustelidae support the social intelligence hypothesis.
Subject(s)
Otters/physiology , Vocalization, Animal , Acoustics , Age Factors , Agonistic Behavior , Animals , Brazil , Emotional Intelligence , Feeding Behavior , Female , Grooming , Male , Models, Psychological , Otters/psychology , Social Behavior , Sound Spectrography , TerritorialityABSTRACT
Tool-use research has focused primarily on land-based animals, with less consideration given to aquatic animals and the environmental challenges and conditions they face. Here, we review aquatic tool use and examine the contributing ecological, physiological, cognitive and social factors. Tool use among aquatic animals is rare but taxonomically diverse, occurring in fish, cephalopods, mammals, crabs, urchins and possibly gastropods. While additional research is required, the scarcity of tool use can likely be attributable to the characteristics of aquatic habitats, which are generally not conducive to tool use. Nonetheless, studying tool use by aquatic animals provides insights into the conditions that promote and inhibit tool-use behaviour across biomes. Like land-based tool users, aquatic animals tend to find tools on the substrate and use tools during foraging. However, unlike on land, tool users in water often use other animals (and their products) and water itself as a tool. Among sea otters and dolphins, the two aquatic tool users studied in greatest detail, some individuals specialize in tool use, which is vertically socially transmitted possibly because of their long dependency periods. In all, the contrasts between aquatic- and land-based tool users enlighten our understanding of the adaptive value of tool-use behaviour.
Subject(s)
Dolphins/physiology , Dolphins/psychology , Ecosystem , Otters/physiology , Otters/psychology , Tool Use Behavior , AnimalsABSTRACT
Stereotypic behaviors, indicating poor welfare and studied in a variety of species (especially carnivores), appear related to characteristics of current and past environments. Although North American river otters (Lontra canadensis) often develop abnormal, repetitive, possibly stereotypic behaviors, no published reports describe otter housing and management or characterize how these variables relate to abnormal repetitive behavior (ARB) occurrence. The first author developed surveys to gather data on housing, individual history, management, and the prevalence of ARBs in otters housed in facilities accredited by the Association of Zoos and Aquariums. Consistent with anecdotal evidence that otters are prone to ARBs, 46% of river otters in the study exhibit them. ARBs were mostly locomotor and often preceded feeding. Exhibits where otters were fed and trained housed a greater percentage of nonhuman animals with ARBs. This study supports the Tarou, Bloomsmith, and Maple (2005) report that more hands-on management is associated with higher levels of ARBs because management efforts are only for animals with ARBs. Escape motivation, breeding season, feeding cues, and ability to forage may affect ARBs in river otters and should be investigated.
Subject(s)
Animals, Zoo/psychology , Otters/psychology , Stereotyped Behavior , Animals , Data Collection , Female , Housing, Animal , MaleABSTRACT
Sex differences in spatial cognition have been reported for many species ranging from voles to humans. The range size hypothesis predicts that sex differences in spatial ability will only occur in species in which the mating system selects for differential range size. Consistent with this prediction, we observed sex differences in spatial ability in giant pandas, a promiscuous species in which males inhabit larger ranges than females, but did not observe sex differences in Asian small-clawed otters, a related monogamous species in which males and females share home ranges. These results provide the first evidence of sex differences in spatial ability in the order Carnivora, and are consistent with the range size hypothesis.