Vocal behavior of Great Curassows,a vulnerable Neotropical bird

ABSTRACT The Cracidae rank among the most threatened families of Neotropical birds, and studies of their vocal behavior may help guide conservation and monitoring efforts. We describe the vocal behavior of Great Curassows (Crax rubra), a little‐studied Cracid species currently listed as vulnerable. From 2008 to 2010, we recorded curassows in northwest Costa Rica using both handheld and automated digital recorders. Analysis of recordings revealed that Great Curassows had a vocal repertoire of five call types. Yip and bark calls are sex‐specific alarm calls of short duration (0.12 and 0.08 s, respectively). The descending whistle is a longer duration alarm call (2.18 s) produced primarily by males. The snarl is a short call (0.67 s) associated with a threat display produced by adults with dependent young. The boom call was the most common Great Curassow vocalization, and was given only by males. Boom calls are long (8.86 s), low‐frequency (<150 Hz), multisyllable calls comprised of four stereotyped phrases. Great Curassows often uttered boom calls well before dawn, with a peak in activity at dawn and the hours following. Males produced bouts of repeated boom calls that lasted an average of 35 min, but sometimes continued for more than 5 h. Boom calls were given from February to June, with a peak in late April and early May when breeding begins. Discriminant analysis of boom calls of birds from 10 different locations revealed interindividual variation in call structure that may be useful for bioacoustic monitoring of individuals. Our results suggest that automated recorders might provide a way to monitor the abundance of male curassows because their boom calls are given frequently during the period from February to June and can be detected at distances up to 250 m.     

Variation in chick‐a‐dee calls of bridled titmice (Baeolophus wollweberi): Frequent use of non‐combinatorial calls in a combinatorial calling system

Chick‐a‐dee calls of Poecile (chickadee) and Baeolophus (titmouse) species are complex in terms of the structural composition of note types and the diversity of messages. Studies so far have mainly focused on the calls of various chickadee and just one titmouse species—the tufted titmouse (B. bicolor). To begin to address this lack of titmouse data, our study investigated variation in note composition of calls of bridled titmice (B. wollweberi). We obtained calls from 26 flocks in the Chiricahua Mountains of Arizona in the overwintering flocking period. Bridled titmice produce proportionally more non‐combinatorial call variants than combinatorial call variants. The number of the single noted calls furthermore exceeded the number of multinote calls. In general, structural variation in the combinatorial calls appears to be comparable to calls of better‐studied chickadees and of tufted titmice, although bridled titmice appear to have a unique call length distribution. We also analyzed some behavioral associations with call variation and found that flight behavior and close interactions between individuals were associated with use of specific note types. Finally, we found microgeographic variation in note type use in these calls. We discuss some possible explanations for call complexity in this species.     

Vocal communication in a neotropical treefrog, Hyla ebraccata: Advertisement calls

We studied the vocal communication of Hyla ebraccata in central Panama. The advertisement call of this species consists of a pulsed buzz-like primary note which may be given alone or followed by 1–4 secondary click notes. Primary notes are highly stereotyped, showing little variation within or0 among individuals in dominant frequency, duration, pulse repetition rate or rise time. Males calling in isolation give mostly single-note calls. They respond to playbacks of conspecific calls by increasing calling rates and the proportion of multi-note calls, and by giving synchronized calls 140–200 ms after the stimulus begins. Responses to conspecific advertisement calls are usually given immediately after the primary note of the leading call, but the primary note of the response often overlaps with the click notes of the leading call. Experiments with synthetic signals showed that males synchronize to any type of sound of the appropriate frequency (3 kHz), regardless of the fine structure of the stimulus. Playbacks of synthetic calls of variable duration showed that males do not synchronize well to calls less than 150 ms long, but they do to longer calls (200–600 ms). The variance in response latency increased with increasing stimulus duration, but modal response times remained at around 140–200 ms. Similar results were obtained in experiments withsynthetic calls having a variable number of click notes. Males showed no tendency to increase the number of click notes in their calls in response to increasing stimulus duration or increasing number of clicks in the stimulus. Females preferred three-note to one-note calls in two-choice playback experiments, whether these were presented in alternation, or with the one-note call leading and the three-note call following. Females showed no preference for leader or follower calls when both were one-note. When two-note calls were presented with the primary note of the follower overlapping the click note of the leader, females went to calls in which click notes were not obscured. Our results indicate that male H. ebraccata respond to other males in a chorus in ways which enhance their ability to attract mates.     

Evolutionary and neurobiological implications of selective phonotaxis in the spring peeper (Hyla crucifer)

Males of the spring peeper (Hyla crucifer) in central Missouri produce frequency-modulated, sinusoidal advertisement calls with a duration of 90–250 ms, and a mid-point frequency of 2800–3360 Hz. The frequency of the call is inversely correlated with body size. In playback experiments with synthetic stimuli, females did not prefer a frequency-modulated call to a call of constant frequency. Females preferred a call with a duration of 150 ms to sounds with durations of 40, 75 and 400 ms; a call of 300 ms was just as attractive as the 150-ms call. Females preferred a call of 2875 Hz to alternatives of 4000 Hz and 2600 Hz. The auditory system of H. crucifer is thus only roughly tuned to the temporal and spectral properties of the advertisement call. The female's specificity with respect to duration alone is adequate for species recognition, but intraspecific mate choice based on call frequency is extremely unlikely.     

Dual Function of Chip Calls Depending on Changing Call Rate Related to Risk Level in Territorial Pairs of White‐Eared Ground‐Sparrows

Different mechanisms have been proposed for encoding information into vocalizations: variation of frequency or temporal characteristics, variation in the rate of vocalization production, and use of different vocalization types. We analyze the effect of rate variation on the dual function of chip calls (contact and alarm) produced by White‐eared Ground‐sparrows (Melozone leucotis). We conducted an acoustic playback experiment where we played back 1 min of four chip call rates (12, 36, 60, 84 calls/min). We measured the response of territorial pairs using behavioral responses, and fine structural features of calls produced in response to those playbacks. White‐eared Ground‐sparrows showed more intense behavioral responses to higher than lower call rate playbacks. Both individuals of the pair approached the source of the playback stimulus faster, produced the first vocalization faster, produced more vocalizations, and spent more time close to the stimulus in higher call rate than in lower call rate playbacks. Frequency and duration characteristics of calls (chip and tseet) were similar in response to all call rate playbacks. Our playback experiment elicited different intensity of behavioral responses, suggesting that risk‐based information is encoded in call rate. Our results suggest that variation in the rate of chip call production serves a dual function in this species; calls are used at lower rates for pair contact and at higher rates for alarm/mobbing signals.     

Is there variation in the response to contact call playbacks across the hybrid zone of the parrot Platycercus elegans?

Learned vocal signals could be important in the formation of prezygotic isolation between two hybridising taxa. This study examined whether vocal variation in the parrot Platycercus elegans facilitates the separation of individuals from two subspecies, P. e. elegans (CR) and P. e. flaveolus (YR). CR and YR have very different plumage coloration, respectively deep crimson and pale yellow, but hybridise where they meet creating an intermediate population (WS). In a factorial design playback experiment, we conducted 108 playback trials on three focal populations (YR, WS, CR), in and around this area of hybridisation, to test if they respond differently to contact calls from their own or another population. We also analysed whether differences in acoustic variables of the stimulus calls predicted the response to the call. We did not find any indication that individuals from the three focal populations responded differently to calls sampled from their own or another subspecies. We did find an effect of two of the five acoustic variables that we used to describe and classify contact calls from the three source populations. Specifically, duration of the stimulus call positively affected the response from individuals from WS and negatively the response from CR, and CR responded more to stimulus calls with a lower peak frequency. Overall, we found no indication that acoustic variation in contact calls on a subspecies level is involved in maintaining plumage colour differences between P. e. elegans and P. e. flaveolus subspecies.     

Crepuscular Changes in Emission Rate and Parameters of the Boatwhistle Advertisement Call of the Gulf Toadfish, Opsanus Beta

We quantified crepuscular variation in the emission rate and call properties of the boatwhistle advertisement call of Gulf toadfish, Opsanus beta, from a field recording of a natural population of nesting males in the Florida Keys. Their calls are more variable and complex than previously reported. A call typically starts with a grunt followed by one to five tonal boop notes (typically two or three) and lasts for over a second. The first boop is considerably longer than later ones, and intervals between boops are relatively constant until the final interval, which approximately doubles in duration. Positions of fish are fixed and calls are sufficiently variable that we could discern individual callers in field recordings. Calling rate increases after sunset when males tend to produce shorter calls with fewer notes. Analysis by number of notes per call indicates some individuals decrease the number of initial grunts and the duration of the first note, but most of the decrease results from fewer notes. To our knowledge this sort of call plasticity has not been demonstrated before in fishes. We suggest that call shortening lowers the chances of overlapping calls of other males and that the small amount of time actually spent producing sound (total on time) is an adaptation to prevent fatigue in sonic muscles adapted for speed but not endurance.     

Sound production in the whitemouth croaker and relationship between fish size and disturbance call characteristics

The whitemouth croaker produces two different sounds using extrinsic sonic muscles: (1) male advertisement calls during the spawning season and (2) disturbance calls, produced by both sexes. The advertisement call, related to courtship, was recorded in the field and from two marked spawning males of 28 and 30.5 cm L_T in the laboratory. It consists of individual pulses with average durations of 19.7 ms and 17.8 ms for the two males respectively, interpulse intervals of 496 ms and 718 ms, and dominant frequencies of 280 Hz and 316 Hz. Pulses are emitted in bouts of one to three min duration. Disturbance calls consist of a burst of pulses produced at short intervals, and the pulse duration, interpulse interval and dominant frequency of the pulses average 19.8 ms, 17.1 ms, and 363 Hz, respectively. Dominant frequency and interpulse interval decrease and pulse duration increases with fish size. Sound characteristics change markedly in young of the year individuals (lower than 25 cm L_T) after which they appear to stabilize. Higher dominant frequency in the advertisement than in the disturbance call and the relationship of dominant frequency to pulse duration suggest that dominant frequency is determined as a forced response to muscle contraction parameters rather than by the natural frequency of the swimbladder.