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.

Vocalizations of European Honey Buzzards (Pernis apivorus) in Southern Africa

Contrary to some sources, the European Honey Buzzard is not silent in Africa. This study documents 51 records of the species vocalizing on the continent. Vocalizations were given by birds apparently encountered alone (n=30) and when accompanied by another European Honey Buzzard (n=22). Where age was known, 11 calling birds were adults and ten were juveniles. Where details were available, most calls were given by birds in flight (n=30), with 11 from perched birds and two from birds heard calling while both in flight and perched. In most cases the sex of the bird was not recorded (n=42) and young birds (first- and second-years) are difficult to sex with certainty; of the remainder, two were males and nine were females. Most calls were the typical flight call of the species (n=43), with apparent alarm calls (n=7) the next most frequent call type. Most calls were delivered in flight (n=31), 19 by single birds and 12 by two birds together in flight. The calling by two birds was associated with flight displays similar to those described on the breeding grounds and occurred especially in late summer (December onwards; 25/40 records). A relatively high proportion of calls occurred during interactions between two European Honey Buzzards (n=18). Calling associated with two birds together and accompanied by aerial displays has not been described in Africa before, and is suggestive of either early pairing of the adult birds prior to migration or breeding activity locally in Africa. Vocalizations between young birds though may be more social as opposed to sexual in nature. The large (5X) increase in records of European Honey Buzzards in South Africa in recent years likely increases the chances of conspecific interaction. It also raises the possibility of breeding, especially in more-temperate South Africa.

A small vocal repertoire during the breeding season expresses complex behavioral motivations and individual signature in the common coot

Background Although acoustic communication plays an essential role in the social interactions of Rallidae, our knowledge of how Rallidae encode diverse types of information using simple vocalizations is limited. We recorded and examined the vocalizations of a common coot (Fulica atra) population during the breeding season to test the hypotheses that 1) different call types can be emitted under different behavioral contexts, and 2) variation in the vocal structure of a single call type may be influenced both by behavioral motivations and individual signature. We measured a total of 61 recordings of 30 adults while noting the behavioral activities in which individuals were engaged. We compared several acoustic parameters of the same call type emitted under different behavioral activities to determine how frequency and temporal parameters changed depending on behavioral motivations and individual differences. Results We found that adult common coots had a small vocal repertoire, including 4 types of call, composed of a single syllable that was used during 9 types of behaviors. The 4 calls significantly differed in both frequency and temporal parameters and can be clearly distinguished by discriminant function analysis. Minimum frequency of fundamental frequency (F0min) and duration of syllable (T) contributed the most to acoustic divergence between calls. Call a was the most commonly used (in 8 of the 9 behaviors detected), and maximum frequency of fundamental frequency (F0max) and interval of syllables (TI) contributed the most to variation in call a. Duration of syllable (T) in a single call a can vary with different behavioral motivations after individual vocal signature being controlled. Conclusions These results demonstrate that several call types of a small repertoire, and a single call with function-related changes in the temporal parameter in common coots could potentially indicate various behavioral motivations and individual signature. This study advances our knowledge of how Rallidae use “simple” vocal systems to express diverse motivations and provides new models for future studies on the role of vocalization in avian communication and behavior.

Context-specific behavior serves as a mechanism of interspecific cohesion in mixed-species flocks

We investigated whether context-specific behavior is responsible for the cohesion of mixed-species flocks of antshrikes and antwrens in Amazonian Peru. Antshrikes perform a behavior while spatially repositioning, to which antwrens respond by approaching. The cohesion of interspecific associations requires communication, although the mechanisms often are unexplored. In monospecific groups, cohesion among individuals is maintained with actions or vocalizations given in a certain context. Dusky-throated Antshrikes (Thamnomanes ardesiacus) vocalize while in flight and the number of times they vocalize covaries with the flight distance. We refer to this pairing of flight and vocalization as repositioning behavior. Furthermore, antshrikes pair a different call type with perching, which we refer to as perching behavior. We followed Long-winged (Myrmotherula longipennis) and White-flanked Antwrens (M. axillaris) and recorded their response following natural vocalizations (no playback used) given by the antshrikes. Long-winged Antwrens, but not White-flanked, flew toward an antshrike significantly sooner and were more likely to approach the antshrikes after the repositioning behavior than after perching behavior. In addition, Long-winged Antwrens, but not White-flanked, flew toward an antshrike sooner after a longer series of repositioning calls than after a shorter series. We did not distinguish between the Long-winged Antwrens’ response as a function of movement vs. vocalizations of the antshrikes, although we argue that vocalizations are likely a more important communication component of repositioning behavior than movement. It remains unclear whether the antshrikes are deliberately signaling the Long-winged Antwrens or the antwrens are taking advantage of the repositioning behavior; active signaling is possible since antshrikes benefit from antwrens. White-flanked Antwrens may be less responsive to the antshrikes since they have a lower propensity to occur in a mixed-species flock. The results indicate that the repositioning behavior of Dusky-throated Antshrikes is a key mechanism of interspecific cohesion of Amazonian mixed-species flocks of the understory.

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.

Acoustilytix™: A Web-Based Automated Ultrasonic Vocalization Scoring Platform

Ultrasonic vocalizations (USVs) are known to reflect emotional processing, brain neurochemistry, and brain function. Collecting and processing USV data is manual, time-intensive, and costly, creating a significant bottleneck by limiting researchers’ ability to employ fully effective and nuanced experimental designs and serving as a barrier to entry for other researchers. In this report, we provide a snapshot of the current development and testing of Acoustilytix™, a web-based automated USV scoring tool. Acoustilytix implements machine learning methodology in the USV detection and classification process and is recording-environment-agnostic. We summarize the user features identified as desirable by USV researchers and how these were implemented. These include the ability to easily upload USV files, output a list of detected USVs with associated parameters in csv format, and the ability to manually verify or modify an automatically detected call. With no user intervention or tuning, Acoustilytix achieves 93% sensitivity (a measure of how accurately Acoustilytix detects true calls) and 73% precision (a measure of how accurately Acoustilytix avoids false positives) in call detection across four unique recording environments and was superior to the popular DeepSqueak algorithm (sensitivity = 88%; precision = 41%). Future work will include integration and implementation of machine-learning-based call type classification prediction that will recommend a call type to the user for each detected call. Call classification accuracy is currently in the 71–79% accuracy range, which will continue to improve as more USV files are scored by expert scorers, providing more training data for the classification model. We also describe a recently developed feature of Acoustilytix that offers a fast and effective way to train hand-scorers using automated learning principles without the need for an expert hand-scorer to be present and is built upon a foundation of learning science. The key is that trainees are given practice classifying hundreds of calls with immediate corrective feedback based on an expert’s USV classification. We showed that this approach is highly effective with inter-rater reliability (i.e., kappa statistics) between trainees and the expert ranging from 0.30–0.75 (average = 0.55) after only 1000–2000 calls of training. We conclude with a brief discussion of future improvements to the Acoustilytix platform.

Semigenerated Carnot algebras and applications to sub-Riemannian perimeter

This paper contributes to the study of sets of finite intrinsic perimeter in Carnot groups. Our intent is to characterize in which groups the only sets with constant intrinsic normal are the vertical half-spaces. Our viewpoint is algebraic: such a phenomenon happens if and only if the semigroup generated by each horizontal half-space is a vertical half-space. We call semigenerated those Carnot groups with this property. For Carnot groups of nilpotency step 3 we provide a complete characterization of semigeneration in terms of whether such groups do not have any Engel-type quotients. Engel-type groups, which are introduced here, are the minimal (in terms of quotients) counterexamples. In addition, we give some sufficient criteria for semigeneration of Carnot groups of arbitrary step. For doing this, we define a new class of Carnot groups, which we call type $$(\Diamond )$$ ( ◊ ) and which generalizes the previous notion of type $$(\star )$$ ( ⋆ ) defined by M. Marchi. As an application, we get that in type $$ (\Diamond ) $$ ( ◊ ) groups and in step 3 groups that do not have any Engel-type algebra as a quotient, one achieves a strong rectifiability result for sets of finite perimeter in the sense of Franchi, Serapioni, and Serra-Cassano.

Policing and public health calls for service in Philadelphia

This contribution outlines various spatial and temporal aspects of medical or public-health related calls for service from the public to police in Philadelphia in 2019. These incidents comprise about 8% of the police department’s workload that originates from the public. Calls appear to be highly concentrated in a few areas, and specifically the Center City and Kensington neighborhoods. They are also more likely to occur late afternoon and evening. The article shows that some medical or public health activity initially masquerades as crime or other policing work and some events eventually determined to be police/crime activity can initially appear to be public health related. About 20% of activity in this area does not appear predictable from the initial call type as handled by police dispatch.

Rutting vocal display in male impala (Aepyceros melampus) and overlap with alarm context

Background The rutting vocal display of male impala Aepyceros melampus is unique for its complexity among ruminants. This study investigates bouts of rutting calls produced towards potential mates and rival males by free-ranging male impala in Namibia. In particular, a comparison of male rutting and alarm snorts is conducted, inspired by earlier findings of mate guarding by using alarm snorts in male topi Damaliscus lunatus. Results Rutting male impala produced 4–38 (13.5 ± 6.5) rutting calls per bout. We analyzed 201 bouts, containing in total 2709 rutting calls of five types: continuous roars produced within a single exhalation-inhalation cycle; interrupted roars including few exhalation-inhalation cycles; pant-roars distinctive by a pant-phase with rapidly alternating inhalations and exhalations; usual snorts lacking any roar part; and roar-snorts starting with a short roar part. Bouts mostly started and ended with usual snorts. Continuous roars were the shortest roars. The average duration of the exhalatory phase was longest in the continuous roars and shortest in the pant-roars. The average fundamental frequency (49.7–51.4 Hz) did not differ between roar types. Vocal tract length, calculated by using measurements of the first four vocal tract resonances (formants), ranged within 381–382 mm in all roar types. In the studied male impala, rutting snorts within bouts of rutting calls were longer and had higher values of the upper quartile in the call spectra than alarm snorts produced towards potential danger. Conclusions Additional inhalations during the emission of the interrupted and pant-roars prolong their duration compared to the continuous roars but do not affect the fundamental frequency or the degree of larynx retraction while roaring. Alarm snorts are separated from one another by large intervals, whereas the intervals between rutting snorts within bouts are short. Sometimes, rutting snorts alternate with roars, whereas alarm snorts do not. Therefore, it is not the acoustic structure of individual snorts but the temporal sequence and the occasional association with another call type that defines snorts as either rutting or alarm snorts. The rutting snorts of male impala may function to attract the attention of receptive females and delay their departure from a male’s harem or territory.