Publications

Abstract

Formants, or resonance frequencies of the upper vocal tract, are an essential part of acoustic communication. Articulatory gestures—such as jaw, tongue, lip, and soft palate movements—shape formant structure in human vocalizations, but little is known about how nonhuman mammals use those gestures to modify formant frequencies. Here, we report a case study with an adult male harbor seal trained to produce an arbitrary vocalization composed of multiple repetitions of the sound wa. We analyzed jaw movements frame-by-frame and matched them to the tracked formant modulation in the corresponding vocalizations. We found that the jaw opening angle was strongly correlated with the first (F1) and, to a lesser degree, with the second formant (F2). F2 variation was better explained by the jaw angle opening when the seal was lying on his back rather than on the belly, which might derive from soft tissue displacement due to gravity. These results show that harbor seals share some common articulatory traits with humans, where the F1 depends more on the jaw position than F2. We propose further in vivo investigations of seals to further test the role of the tongue on formant modulation in mammalian sound production.

Abstract

Vocal development of cranes (Gruidae) has attracted scientifc interest due to its special stage, voice breaking. During voice breaking, chicks of diferent crane species produce calls with two fundamental frequencies that correspond to those in adult low-frequency and juvenile high-frequency vocalizations. However, triggers that afect voice breaking in cranes are mainly unknown. Here we studied the voice breaking in the Siberian Crane (Leucogeranus leucogeranus) and test its relation to the body mass and testosterone level. We analyzed 5846 calls, 39 body mass measurements and 60 blood samples from 11
Siberian Crane chicks in 8 ages from 2.5 to 18 months of life together with 90 body mass measurements and 61 blood samples from 24 Siberian Crane adults. The individual duration of voice breaking and dates of its onset, culmination and completion depended neither on the body mass nor on the testosterone level at various ages. But we found correlation between the testosterone level and mean deltas of percentages of the high and low frequency components in Siberian Crane calls between the closest recording sessions. We also observed some coincidence in time between the mean dates of voice breaking onset and the termination of body mass gain (at 7.5 months of age), and between the mean dates of voice breaking completion and the start of a new breeding season. Similar relations have been shown previously for some other crane species. We also showed for the frst time that the mean dates of voice breaking culmination correlated with the signifcant increase of the testosterone level (at 10.5 months of age). So, we suggest that voice breaking in cranes may be triggered by the end of chicks’ body
growth, is stimulated by the increase of testosterone level and ends soon after adult cranes stop taking care of their chicks.

Abstract

Vocal-based monitoring is increasingly being used as a non-invasive method for identifying individuals within avian populations and is promising for the Siberian Crane, Leucogeranus leucogeranus. This is a poorly studied, long-lived, secretive and critically endangered bird species that breeds in the Arctic tundra of western and eastern regions of Siberia. We assessed between- and within-year stability of individual-specific vocal features in duets of Siberian Crane and tested the effect of pair-mate change on their stability. Previous findings showed that duets are specific to different pairs of birds; however, it is still unknown how long pair-specific traits of duets remain and if they change in the course of a year or when birds re-mate. We recorded duets of 15 reproductively active pairs in the Oka Crane Breeding Centre in 2003–2006 and 2013–2017. We found that pair-specific vocal signatures remained stable both within the year and across ~ 10 years. After a change of mate, most of the variables we measured in the call did not change in any of the birds. Our data suggest that the stability of the
individually specific vocal features may enable Siberian Cranes to be reliably identified by their duets over the birds’ lifetime. We believe that our work can increase confidence in the use of acoustic recognition techniques for endangered crane monitoring programs. Our results also suggest that Siberian Cranes may use their duets to form long-term social bonds between neighbours.

Abstract

Chicks can convey information about their needs with calls. But it is still unknown if there are any universal need indicators in chick vocalizations. Previous studies have shown that in some species vocal activity and/or temporal-frequency variables of calls are related to the chick state, whereas other studies did not confirm it. Here, we tested experimentally whether vocal activity and temporal-frequency variables of calls change with cooling. We studied 10 human-raised
Siberian crane (Grus leucogeranus) chicks at 3–15 days of age. We found that the cooled chicks produced calls higher in fundamental
frequency and power variables, longer in duration and at a higher calling rate than in the control chicks. However, we did not find
significant changes in level of entropy and occurrence of non-linear phenomena in chick calls recorded during the experimental cooling. We suggest that the level of vocal activity is a universal indicator of need for warmth in precocial and semi-precocial birds (e.g. cranes), but not in altricial ones. We also assume that coding of needs via temporal-frequency variables of calls is typical in species whose adults could not confuse their chicks with other chicks. Siberian cranes stay on separate territories during their breeding season, so parents do not need to check individuality of their offspring in the home area. In this case, all call characteristics are available for other purposes and serve to communicate chicks’ vital needs.

Abstract

Vocal individuality provides a method of personalization for multiple avian species. However, expression of individual vocal features depends on necessity of recognition. Here we focused on chick vocalizations of demoiselle, Siberian and red-crowned cranes that differ by their body size, developmental rates and some ecological traits. Cranes are territorial during summer, but gather in
large flocks during autumn and winter. Nevertheless, parents keep feeding their chicks, even on winter grounds, despite the potential of confusing their own and alien
chicks. Here we aimed to compare expression of individuality and sex in calls of three crane species between solitary and gregarious periods of a chick’s life, and between species. We found significant individual patterns of
acoustic variables in the calls of all three species both before and after fledging. However, only red-crowned crane chicks increased expression of individuality significantly after the fledging. Also, we found that chicks of all three species significantly increased occurrence of nonlinear phenomena, i.e., irregular oscillations of soundproducing membranes (biphonations, sidebands, and deterministic chaos), in their calls after fledging. Non-linear phenomena can be a way of increasing the potential for
individual recognition as well as avoiding habituation of parents to their chicks’ calls. The older chicks are, the less
their parents feed them, and chicks benefit from keeping the permanent attention.

Abstract

The vocal development of cranes (Gruidae) has attracted scientific interest due to a
special stage, so-called voice breaking. During voice breaking, chicks produce both
adult low-frequency and juvenile high-frequency vocalizations. The triggers that affect voice breaking are unknown. For the first time, we study the vocal development of the Demoiselle Crane (Anthropoides virgo). We describe the age and possible drivers of
the onset of voice breaking. We analyse the calls of 21 Demoiselle Crane chicks, and
compare them with the calls of six adult birds, noting the day when adult low-frequency calls are first recorded as the day when voice breaking begins. The age of voice
breaking onset does not depend on hatching date, clutch order or chick body mass. Thus, there is no correlation between body growth and the onset of voice breaking for individual Demoiselle Crane chicks. However, there is a strong relationship between body mass and voice breaking among different crane species. Demoiselle Cranes stop intense body growth at the age of 2 months and start voice breaking at 70 ^ 46 days. By way of comparison, Red-crowned Cranes finish the period of intense body growth at the age of 7 months and start voice breaking at 211 ^ 60 days. Thus, we show that the Demoiselle Crane has a sudden vocal development, similar to other crane species, and we suggest that the end of intense body growth is the trigger for the onset of voice breaking in cranes.