It's All About the Heart

This chapter aimed to provide responses, within the issue of cardiovascular health, to the effectiveness of the relation between the message's content (“what”) and form (“how”) and the triad of (cognitive-affective-behavioral) effects. The qualitative content analysis, concretely thematic and rhetorical types, was applied to a corpus of five ads from international campaigns (2015-2019) and three static Portuguese ads (2018-2019). One online survey of Portuguese university students (N = 55) was conducted. The findings show that the ads' issues vary from irreparable losses to the encouragement of healthy behaviors. The pathos tends to elicit various reactions (e.g., alarm, call to action, empathy, fear, guilt, hurt, worry). The logos are constructed of discursive devices (e.g., construction of a narrative, use of questions, selection of colors with connotative purposes, descriptions of concepts), evidence, and stylistic devices. Most of the respondents recognize the cognitive and affective influence, but not the behavioral effects.

Parent-offspring and inter-offspring responses to conspecific vs heterospecific distress calls in two sympatric birds

Distress calls, as a type of alarm call, play important roles in expressing bodily condition and conveying information concerning predation threats. In this study, we examined the communication via distress calls in parent–offspring and inter-offspring interactions. First, we used playback of chick distress calls of two sympatric breeders, the vinous-throated parrotbill Sinosuthora webbiana and the oriental reed warbler Acrocephalus orientalis, to the adults/chicks of these two species respectively and measured the responses of conspecifics or heterospecifics. The playback-to-chicks experiment showed that both species of chicks reduced the number of begging calls and begging duration time as a response to conspecific/heterospecific distress calls compared with natural begging and background noise controls. However, reed warbler chicks also reduced beak opening frequency in the response to conspecific distress calls compared with other playback stimuli. Second, the results of the playback-to-adults experiment showed that reed warbler adults could eavesdrop on distress calls of conspecific neighbors and sympatric heterospecifics. Furthermore, the nest-leaving behavior of reed warblers did not differ significantly when they heard the distress calls of conspecifics or parrotbills. Finally, reed warbler adults responded to conspecific distress calls more quickly than to heterospecific distress calls, while parrotbill adults presented the opposite response. Our results supported the warn-kin hypothesis and show that chick distress calls play an important role in conveying risk and the condition of chicks to enhance individual fitness. In addition, we also found that eavesdropping on distress calls is a congenital behavior that begins in the chick stage.

Discrimination of Acoustic Stimuli and Maintenance of Graded Alarm Call Structure in Captive Meerkats

Animals living in human care for several generations face the risk of losing natural behaviors, which can lead to reduced animal welfare. The goal of this study is to demonstrate that meerkats (Suricata suricatta) living in zoos can assess potential danger and respond naturally based on acoustic signals only. This includes that the graded information of urgency in alarm calls as well as a response to those alarm calls is retained in captivity. To test the response to acoustic signals with different threat potential, meerkats were played calls of various animals differing in size and threat (e.g., robin, raven, buzzard, jackal) while their behavior was observed. The emitted alarm calls were recorded and examined for their graded structure on the one hand and played back to them on the other hand by means of a playback experiment to see whether the animals react to their own alarm calls even in the absence of danger. A fuzzy clustering algorithm was used to analyze and classify the alarm calls. Subsequently, the features that best described the graded structure were isolated using the LASSO algorithm and compared to features already known from wild meerkats. The results show that the graded structure is maintained in captivity and can be described by features such as noise and duration. The animals respond to new threats and can distinguish animal calls that are dangerous to them from those that are not, indicating the preservation of natural cooperative behavior. In addition, the playback experiments show that the meerkats respond to their own alarm calls with vigilance and escape behavior. The findings can be used to draw conclusions about the intensity of alertness in captive meerkats and to adapt husbandry conditions to appropriate welfare.

Vocalization of Western Tarsier (Cephalopachus bancanus Horsfield, 1821) in Bangka Island, Indonesia

Every tarsier species performs different vocalization behaviour. Cephalopachus bancanus as one of the tarsier species listed as vulnerable in the IUCN red list has limited and different information about their vocalization. This research was designed to explore the species vocalization in the vicinity of Petaling Village, District of Bangka, Bangka Island, Indonesia. Tarsier vocalization inside temporary enclosures was recorded using a handy recorder and analysed using bioacoustics software Audacity 2.3.3 and Raven Pro 1.6.1. We described seven vocalization types with different functions and spectrogram patterns. One type of vocalization, squeak, is produced only by the infant. Two types of vocalizations (whistle and cheeps) were produced by the infant and adult, and four vocalization types were performed by adults. Those types of vocalizations can be heard within human hearing. Some types of vocalizations have peak frequencies at the ultrasonic level, i.e.: agonistic scream, alarm call, distress call, and hysteresis.

The cessation of contact calls does not provoke or modulate alarm behaviour in a social passerine

Vocalizations that signal predation risk such as alarm calls provide crucial information for the survival of group-living individuals. However, alarm calling may attract the predator’s attention and, to avoid this cost, animals can opt for alternative strategies to indicate danger, such as ‘adaptive silence’, which is the cessation of vocalizations. We investigate here whether abrupt contact call cessation would provoke alarm responses, or would reinforce the signal given by an alarm call. In an aviary setting, we conducted playback experiments with a group-living passerine, the Swinhoe’s white-eye, Zosterops simplex. We found that birds did not respond to a sudden call cessation, nor did they have a stronger response to alarm calls followed by silence than to alarm calls followed by contact calls. Confirming previous work investigating contact call rate, it appears that in this species contact calls encode information about social factors but not environmental conditions.

The Role of Acoustics in the Conservation of the Ivory-Billed Woodpecker (Campephilus principalis)

The Ivory-billed Woodpecker (Campephilus principalis) is an iconic species that has survived in barely detectable numbers for the past 100 years, during which it has been feared extinct only to be rediscovered several times. The most recent rediscovery was announced in an article that was featured on the cover of Science in 2005. The persistence of the Ivory-billed Woodpecker became controversial when ornithologists were unable to obtain a clear photo for documenting this ultra-elusive bird during multi-year searches at sites in Arkansas and Florida, where they had several sightings and were convinced these birds were present. Audio recordings of ‘kent’ calls and double knocks were obtained at both sites, but such recordings are not regarded as conclusive evidence of persistence. A debate on this issue that took place in Science and Nature focused on relatively weak video evidence obtained in Arkansas but excluded three videos obtained in Louisiana and Florida that show flights, field marks, and other behaviors and characteristics that are consistent with the Ivory-billed Woodpecker but no other species of the region. Kent calls were recorded in the 1930s, when other types of vocalizations were observed but not recorded, including a high-pitched alarm call. On two occasions in Louisiana, high-pitched calls were observed coming from the direction of an alarmed Ivory-billed Woodpecker, and several of them were recorded. The spectrograms of the high-pitched calls and all other known and putative vocalizations of the Ivory-billed Woodpecker consist of simultaneously excited harmonics. A harmonic oscillator model has been used to draw a connection between the drumming that is typical of most woodpeckers and the double knocks of the Ivory-billed Woodpecker and other Campephilus woodpeckers. Drumming corresponds to periodic forcing; double knocks correspond to impulsive forcing, and a single thrust of the body is sufficient to produce two impacts of the bill in rapid succession. The audio recordings from Arkansas and Florida were obtained with single microphones. A horizontal array of microphones would make it possible to detect weaker sounds and determine the directions of sources. This approach has the potential to lead to the discovery of a nest, and it might be more effective if the array is placed above the treetops, where sounds might propagate to longer ranges.

A study on the role of social information sharing leading to range expansion in songbirds with large vocal repertoires: Enhancing our understanding of the Great-tailed Grackle (Quiscalus mexicanus) alarm call

The acoustic adaptation hypothesis posits that animal sounds are influenced by the habitat properties that shape acoustic constraints (Ey and Fischer 2009, Morton 2015, Sueur and Farina 2015).Alarm calls are expected to signal important habitat and receiver-dependent information (Ripmeester et al. 2010, Sheldon et al. 2020), and we want to test whether Q. mexicanus alarm calls differ between populations and ecological contexts across the US as expected under the acoustic adaptation hypothesis (three US subspecies: Q. m. nelsoni, Q. m. monsoni, and Q. m. prospidicola; Figure 1). The alarm call vocalization in Q. mexicanus is known to vary in tone, range and pitch (Kok 1971). Alarm calls signal low intensity excitement (Kok 1971) and research in other species has shown that differences in the acoustic qualities of alarm calls reflect the urgency of threats tailored to the receiving audience (Carlson et al. 2020, Sheldon et al. 2020, McLachlan and Magrath 2020). However, due to the ecological importance of alarm calls in minimizing risk to group members, natural selection could promote stabilizing selection on alarm calls, resulting in homogenous alarm call structure across subspecies regardless of habitat and receiver. For this reason, we will also test whether Q. mexicanus songs differ between populations and ecological contexts across the US as natural selection likely promotes disruptive selection on song structure to facilitate subspecies recognition during mating season (Cruz-Yepez et al. 2020, Simpson et al. 2021). In this project we will enhance our understanding of the vocal repertoire of Q. mexicanus, by 1) recording and describing alarm calls and songs, 2) testing a null hypothesis that differing vocalizations will correlate with subspecies-specific soundscapes, and 3) test an alternative hypothesis that vocal signal characteristics correlate with range expansion. We will improve the description of vocalizations by recording vocalizations from each subspecies and analyzing the tone, range and pitch of vocalizations using spectrograms generated with Raven Lite 2.0 (Cornell Lab of Ornithology). Recording of alarm calls will take place during the non-breeding season, and of songs during the breeding season. We will only record alarm calls during the non-breeding period to avoid differences associated with reproduction. For our first objective, a phylogenetic principal component analysis (PPCA) will be conducted to identify correlations among measures of vocalization structure across subspecies while accounting for phylogenetic history. For our second objective, a phylogenetic generalized least squares analysis (PGLS) will be conducted to determine if subspecies vocalization characteristics are explained by social and habitat contexts within a phylogenetic context. To test whether vocalizations have functionally diverged and to help explain differences in range expansion, we will conduct a reciprocal playback experiment measuring responsiveness to recordings from within each subspecies compared to those from other subspecies. We will use the results of the PPCA and playback experiment to test whether vocal signal characteristics (both signal and response) are significant regional drivers of predicted distributions for Q. mexicanus in the US using an ensemble distribution model. If vocal signal skill is learned from context-dependent experiences unique to each subspecies (i.e., in line with the acoustic adaptation hypothesis), then individuals should share vocal characteristics with and respond to the signals of their own subspecies but not to signals of other subspecies. Tone, range, and pitch of vocalizations as well as low responsiveness will be a significant explanatory variable in all regional models (i.e., differences in vocal signals will distinguish subspecies distributions). However, if differences in regional models are due to variation in responsiveness according to subspecies, then skill in vocal communication could contribute to differences in range expansion among subspecies....

Lesser spot-nosed monkeys coordinate alarm call production with associated Campbell’s monkeys

Forest monkeys often form semi-permanent mixed-species associations to increase group-size related anti-predator benefits without corresponding increases in resource competition. In this study, we analysed the alarm call system of lesser spot-nosed monkeys, a primate that spends most of its time in mixed-species groups while occupying the lowest and presumably most dangerous part of the forest canopy. In contrast to other primate species, we found no evidence for predator-specific alarm calls. Instead, males gave one general alarm call type (‘kroo’) to three main dangers (i.e., crowned eagles, leopards and falling trees) and a second call type (‘tcha-kow’) as a coordinated response to calls produced in non-predatory contexts (‘boom’) by associated male Campbell’s monkeys. Production of ‘kroo’ calls was also strongly affected by the alarm calling behaviour of male Campbell’s monkeys, suggesting that male lesser spot-nosed monkeys adjust their alarm call production to another species’ vocal behaviour. We discuss different hypotheses for this unusual phenomenon and propose that high predation pressure can lead to reliance on other species vocal behaviour to minimise predation. Significance statement Predation can lead to the evolution of acoustically distinct, predator-specific alarm calls. However, there are occasional reports of species lacking such abilities, despite diverse predation pressure, suggesting that evolutionary mechanisms are more complex. We conducted field experiments to systematically describe the alarm calling behaviour of lesser spot-nosed monkeys, an arboreal primate living in the lower forest strata where pressure from different predators is high. We found evidence for two acoustically distinct calls but, contrary to other primates in the same habitat, no evidence for predator-specific alarms. Instead, callers produced one alarm call type (‘kroo’) to all predator classes and another call type (‘tcha-kow’) to non-predatory dangers, but only as a response to a specific vocalisation of Campbell’s monkeys (‘boom’). The production of both calls was affected by the calling behaviour of Campbell’s monkeys, suggesting that lesser spot-nosed monkey vocal behaviour is dependent on the antipredator behaviour of other species. Our study advances the theory of interspecies interactions and evolution of alarm calls.

Aping Language: Historical Perspectives on the Quest for Semantics, Syntax, and Other Rarefied Properties of Human Language in the Communication of Primates and Other Animals

In 1980, Robert Seyfarth, Dorothy Cheney and Peter Marler published a landmark paper in Science claiming language-like semantic communication in the alarm calls of vervet monkeys. This article and the career research program it spawned for its authors catalyzed countless other studies searching for semantics, and then also syntax and other rarefied properties of language, in the communication systems of non-human primates and other animals. It also helped bolster a parallel tradition of teaching symbolism and syntax in artificial language systems to great apes. Although the search for language rudiments in the communications of primates long predates the vervet alarm call story, it is difficult to overstate the impact of the vervet research, for it fueled field and laboratory research programs for several generations of primatologists and kept busy an equal number of philosophers, linguists, and cognitive scientists debating possible implications for the origins and evolution of language and other vaunted elements of the human condition. Now 40-years on, the original vervet alarm call findings have been revised and claims of semanticity recanted; while other evidence for semantics and syntax in the natural communications of non-humans is sparse and weak. Ultimately, we are forced to conclude that there are simply few substantive precedents in the natural communications of animals for the high-level informational and representational properties of language, nor its complex syntax. This conclusion does not mean primates cannot be taught some version of these elements of language in artificial language systems – in fact, they can. Nor does it mean there is no continuity between the natural communications of animals and humans that could inform the evolution of language – in fact, there is such continuity. It just does not lie in the specialized semantic and syntactic properties of language. In reviewing these matters, I consider why it is that primates do not evince high-level properties of language in their natural communications but why we so readily accepted that they did or should; and what lessons we might draw from that experience. In the process, I also consider why accounts of human-like characteristics in animals can be so irresistibly appealing.

The Vocal Repertoire of the Bearded Capuchin (Cebidae: Sapajus libidinosus): Implications for Understanding the Complexity of Neotropical Primate Communication

Vocal communication is an essential aspect of primate social behaviour. The bearded capuchin <i>Sapajus libidinosus</i> is endemic to Brazil, and some studies have described specific vocalisation types for this species; however, there is still no complete description of its vocal repertoire. Thus, this study aimed to describe the vocal repertoire of a group of <i>S. libidinosus</i> living in the<i></i>Parque Nacional de Brasília, a protected area in the Cerrado area of Central Brazil. We carried out focal samplings and recording of vocalisations of members of an <i>S. libidinosus</i> troop in different behavioural contexts. The call analyses revealed 25 different types of vocalisations, and each call presented significant structural variation. We grouped these vocalisations according to the context of the emission or acoustic structure into the following categories: contact calls (contact note, infant babbling, trill, teeth- and lip-smacking, and sirena); foraging calls (chihui, grgr, and patinado); whistle series (food-associated, long-distance, and intergroup encounter); aggressive calls (aggressive contact note, ascending rapid staccato, cough cough, and pip); calls in response to aggression (scream, squeal, and pulsed scream), sexual display calls (chuck and raspy oestrous call), and stress-related calls (alarm call/bark, hiccup, hip, double hip, and wah wah). <i>S. libidinosus</i> presented a very rich vocal repertoire, revealing a pattern consistent with the repertoire of other capuchin monkey species. This is the first comprehensive description of the<i> S. libidinosus</i> vocal repertoire and highlights the complexity of neotropical primate communication.