A report on a characteristic vocalization in Corvus macrorhynchos osai with an indication of vocal learning

In the process of vocal learning, animals give immature vocalization, such as babbling and subsong. Here I report a characteristic vocalization given by a subspecies of large-billed crow, Corvus macrorhynchos osai, that live in Kuroshima Island, Okinawa, Japan. This vocalization (type-K) is characterized by very rapid bill movements (ca. 13 times/sec). The type-K was heard throughout the island, indicating that the population of the Kuroshima Island share this call type. In addition, a juvenile crow was observed giving immature type-K repeatedly. This observation suggests that this call type is not innate but acquired through vocal learning.

Echolocation reverses information flow in a cortical vocalization network

The mammalian frontal and auditory cortices are fundamental structures supporting vocal behaviour, yet the patterns of information exchange between these regions during vocalization remain unknown. Here, we address this issue by means of electrophysiological recordings in the fronto-auditory network of freely-vocalizing Carollia perspicillata bats. We show that oscillations in frontal and auditory cortices predict vocalization type with complementary patterns across structures. Transfer entropy analyses of oscillatory activity revealed directed information exchange in the circuit, predominantly of top-down nature (frontal to auditory). The dynamics of information flow depended on vocalization type and on the timing relative to vocal onset. Remarkably, we observed the emergence of predominant bottom-up information transfer, only when animals produced calls with imminent post-vocal consequences (echolocation signals). These results unveil changes of information flow in a large-scale sensory and association network associated to the behavioural consequences of vocalization in a highly vocal mammalian model.

Male Carollia perspicillata bats call more than females in a distressful context

Distress calls are a vocalization type widespread across the animal kingdom, emitted when the animals are under duress, e.g. when captured by a predator. Here, we report on an observation we came across serendipitously while recording distress calls from the bat species Carollia perspicillata , i.e. the existence of sex difference in the distress calling behaviour of this species. We show that in C. perspicillata bats, males are more likely to produce distress vocalizations than females when hand-held. Male bats call more, their calls are louder, harsher (faster amplitude modulated) and cover lower carrier frequencies than female vocalizations. We discuss our results within a framework of potential hormonal, neurobiological and behavioural differences that could explain our findings, and open multiple paths to continue the study of sex-related differences in vocal behaviour in bats.

The vocal repertoire of an African colobine, Colobus angolensis ruwenzorii: a multi-level society compared to congeners in stable groups

Vocal behaviour offers a window into understanding the social life and evolution of animals. Colobine monkeys show great interspecific and interpopulation variation in their social organization and behaviour. Recent research has shown that Rwenzori Angolan colobus (Colobus angolensis ruwenzorii) differ substantially from other black-and-white colobus in forming a multi-level society. No previous research has been conducted on the communication of C. a. ruwenzorii, but the social complexity hypothesis for communication suggests that more complex societies should evolve more complex communication repertoires. Our objective was to catalogue the vocal repertoire of C. a. ruwenzorii at Nabugabo, Uganda, and to compare it with the data available on congeners regarding intergroup tolerance, vocal repertoire size, and acoustic and behavioural features of vocal communication. Vocalizations were subject to spectrographic and behavioural analysis, and a descriptive analysis of each vocalization type was made. The influence of a few environmental and social factors on calling rates was also examined. We describe five vocalizations (i.e., the snort, roar, squeak, scream and pok) and one non-vocal signal (i.e., the tongue click) in this subspecies and their contexts. Distinct alarm calls are made for dogs, and these are given more often near the edge of the forest where humans frequent. We did not find that C. a. ruwenzorii showed a greater vocal repertoire than C. guereza or C. polykomos, which do not live in multi-level societies. Further, preliminary data do not indicate greater calling rates in larger core units of C. a. ruwenzorii compared to smaller units. These findings support the view that these primates’ vocalizations tend to be relatively conserved despite large differences in social organization.

Temporal–spatial, spectral, and source level distributions of fin whale vocalizations in the Norwegian Sea observed with a coherent hydrophone array

To better understand fin whale vocalization behaviour in the Norwegian and Barents Seas, a large-aperture densely sampled coherent hydrophone array was deployed in late winter 2014 to monitor their vocalizations instantaneously over wide areas via passive ocean acoustic waveguide remote sensing (POAWRS). Here, we (i) provide a time-frequency characterization for different call types observed (20 Hz pulses, 130 Hz upsweeps, 30–100 Hz downsweep chirps, and 18–19 Hz backbeats); (ii) compare their relative abundances in three different coastal regions off Alesund, Lofoten, and Northern Finnmark; (iii) estimate the temporal and spatial distributions; (iv) source level distributions; and (v) probability of detection (PoD) regions for the more abundant 20 Hz pulse and 130 Hz upsweep call types. The fin whale vocalizations received over the diel cycle (24 h) were significantly more abundant by a factor of roughly seven off Northern Finnmark than the other two regions, associated with fish feeding activities. The source levels are estimated to be 190.5±7.4 dB for the fin whale 20 Hz pulses and 170.3 ± 5.2 dB for the 130 Hz upsweeps. We find that fin whales are capable of producing each vocalization type either independently or simultaneously with other types, and the 20 Hz sound production in the fin whales involves a mechanism that generates a significantly less-intense second-order harmonic of the fundamental.

The aggressive call of Dendropsophus cruzi (Pombal & Bastos, 1998) (Anura; Hylidae) in Central Brazil

Dendropsophus cruzi (Pombal & Bastos, 1998) is a small hylid (male snout-to-vent length = 16.3–19.4 mm; female SVL = 21.3–25.0 mm) that is allocated in the D. microcephalus group (Faivovich et al. 2005). It is commonly found in Open and forested areas from Central Brazil to Provincia Velasco, Departamento de Santa Cruz, Bolivia (Frost 2017; Tessarolo et al. 2016). Pombal & Bastos (1998) described the advertisement call of D. cruzi as a single pulsed note. Posteriorly, studies uncovered relationships between dominant frequency variation in the advertisement calls of D. cruzi and variation in the SVL and mass of males (Bastos et al. 2003), as well as the existence of a clinal geographic pattern in the variation of acoustic parameters of these calls (Tessarolo et al. 2016). However, the acoustic communication in anurans is usually mediated by more than one vocalization type (Toledo et al. 2015). Due the importance of call types in the social context of anurans (e.g., Reichert 2011; Forti et al. 2017), we expand the vocal repertoire of D. cruzi by describing its aggressive call.

Call Usage Learning by a Beluga (Delphinapterus leucas) in a Categorical Matching Task

The ability to modify the structure and context of vocalizations through learning plays a key role in the social interactions of many species. The investigation of categorical matching, an aspect of contextual vocal learning, is the first step toward determining how contextual learning plays a role in the use, comprehension, and categorization of sounds in the wild. To this end, we conducted a study at the Vancouver Aquarium to test the ability of a juvenile female beluga, Qila, to respond to playbacks of two types of in-air beluga calls with vocalizations that matched the category of call played (a scream, which is a vocalization type shaped over time with reinforcement and not part of this species'natural repertoire, and a pulse-train, a natural call category). We first tested Qila with random sequences of the same version of the two vocalizations with which she had been trained. Her overall success in matching all playback stimuli was above chance but not statistically so (66%). She had more difficulty matching screams (54% success) than pulse trains (80% success). We next played random sequences of six novel pulse-trains and seven novel screams, which Qila had not been trained with. She responded correctly to the set of novel stimuli of both call types in 64% of the trials, a success rate that did not differ statistically from chance. Again, she had more difficulty matching screams (55% success), relative to pulse trains (74% success). These results indicate that Qila successfully matched only pulse trains, the class that is part of this species’ natural repertoire. Her poor performance on matching screams might be partly explained by a difficulty to perceive categorically a signal that lacks a function in the natural repertoire of belugas.

Vocal repertoire of adult captive red pandas (Ailurus fulgens)

Vocal signals are a common communication tool used to recognize different individuals, advertise fertile phases or discriminate amongst potential mates. Therefore, a thorough understanding of vocal repertoires forms the basis for investigating the role of acoustic signaling in the sexual and social behavior of any animal. Red pandas (Ailurus fulgens) are classified as a vulnerable species and have declined by as much as 40% over the past 50 years in China. Adult red pandas are known to call frequently during mating and aggressive encounters; however, no quantitative description of their vocalizations has been attempted. Here, the vocal repertoire of captive red pandas was investigated. Acoustical and statistical analyses indicated seven vocalization types during the breeding season: “growl”, “bark”, “squeal”, “bleat”, “hoot”, “grunt” and “twitter”; the spectrogram for each vocalization type was extracted. The type of vocalizations produced varied with behavioral state and implies different functional contexts. Future studies are needed to uncover the functions of red panda vocalizations in individual recognition, sexual selection and social interaction.

High-field Functional Magnetic Resonance Imaging of Vocalization Processing in Marmosets

Vocalizations are behaviorally critical sounds, and this behavioral importance is reflected in the ascending auditory system, where conspecific vocalizations are increasingly over-represented at higher processing stages. Recent evidence suggests that, in macaques, this increasing selectivity for vocalizations might culminate in a cortical region that is densely populated by vocalization-preferring neurons. Such a region might be a critical node in the representation of vocal communication sounds, underlying the recognition of vocalization type, caller and social context. These results raise the questions of whether cortical specializations for vocalization processing exist in other species, their cortical location, and their relationship to the auditory processing hierarchy. To explore cortical specializations for vocalizations in another species, we performed high-field fMRI of the auditory cortex of a vocal New World primate, the common marmoset (Callithrix jacchus). Using a sparse imaging paradigm, we discovered a caudal-rostral gradient for the processing of conspecific vocalizations in marmoset auditory cortex, with regions of the anterior temporal lobe close to the temporal pole exhibiting the highest preference for vocalizations. These results demonstrate similar cortical specializations for vocalization processing in macaques and marmosets, suggesting that cortical specializations for vocal processing might have evolved before the lineages of these species diverged.