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Call Types (call + type)
Selected AbstractsAcoustic Features of Female Chacma Baboon BarksETHOLOGY, Issue 1 2001Julia Fischer We studied variation in the loud barks of free-ranging female chacma baboons (Papio cynocephalus ursinus) with respect to context, predator type, and individuality over an 18-month period in the Moremi Game Reserve, Botswana. To examine acoustic differences in relation to these variables, we extracted a suite of acoustic parameters from digitized calls and applied discriminant function analyses. The barks constitute a graded continuum, ranging from a tonal, harmonically rich call into a call with a more noisy, harsh structure. Tonal barks are typically given when the signaler is at risk of losing contact with the group or when a mother and infant have become separated (contact barks). The harsher variants are given in response to large predators (alarm barks). However, there are also intermediate forms between the two subtypes which may occur in both situations. This finding is not due to an overlap of individuals' distinct distributions but can be replicated within individuals. Within the alarm bark category, there are significant differences between calls given in response to mammalian carnivores and those given in response to crocodiles. Again, there are intermediate variants. Both alarm call types are equally different from contact barks, indicating that the calls vary along different dimensions. Finally, there are consistent, significant differences among different individuals' calls. However, individual identity in one call type cannot directly be inferred from knowledge of the individuals' call characteristics in the other. In sum, the barks of female baboons potentially provide rich information to the recipients of these signals. The extent to which baboons discriminate between alarm and contact barks, and classify calls according to context and/or acoustic similarity will be described in a subsequent paper. [source] The communicative content of the common marmoset phee call during antiphonal callingAMERICAN JOURNAL OF PRIMATOLOGY, Issue 11 2010Cory T. Miller Abstract Vocalizations are a dominant means of communication for numerous species, including nonhuman primates. These acoustic signals are encoded with a rich array of information available to signal receivers that can be used to guide species-typical behaviors. In this study, we examined the communicative content of common marmoset phee calls, the species-typical long distance contact call, during antiphonal calling. This call type has a relatively stereotyped acoustic structure, consisting of a series of long tonal pulses. Analyses revealed that calls could be reliably classified based on the individual identity and social group of the caller. Our analyses did not, however, correctly classify phee calls recorded under different social contexts, although differences were evident along individual acoustic parameters. Further tests of antiphonal calling interactions showed that spontaneously produced phee calls differ from antiphonal phee calls in their peak and end frequency, which may be functionally significant. Overall, this study shows that the marmoset phee call has a rich communicative content encoded in its acoustic structure available to conspecifics during antiphonal calling exchanges. Am. J. Primatol. 72:974,980, 2010. © 2010 Wiley-Liss, Inc. [source] The structure of vocalization of ewes and male lambs at pastureANIMAL SCIENCE JOURNAL, Issue 1 2009Hirofumi NAEKAWA ABSTRACT We performed an analysis of the vocalization of 161 ewes and 50 male lambs that were pastured day and night. The vocalization structures of the phonetic notations of the opened-mouth from closed mouth /,aee/ and /,naeee/ and closed-mouth /,,,,/ of ewes, and the opened-mouth from closed-mouth /,eee/ and /,neeee/ and closed-mouth /,,,,/ of male lambs were studied in terms of their audio characteristics. The items subject to analysis included duration of each vocalization, fundamental frequency, sound pressure and first formant (F1), second formant (F2), and third formant (F3). Among the male lambs, the duration of each call type showed significant differences depending on the behavior types or the target types, and the closed-mouth to open-mouth sounds, /,eee/ and /,neeee/ showed a tendency to be longer than the closed-mouth sound of /,,,,/. A significant correlation (r = 0.9, P < 0.05) was observed between the fundamental frequency and F1 with the /,eee/ type of call of the male lambs when the vocalization was targeted toward the stockperson. When the ewes' behavior pattern was grazing and moving and the calling target was an ewe, the sound pressure significantly differed between /,,,,/ and /,naeee/ (P < 0.05). From the analysis of the call durations, the fundamental frequencies, the sound pressures and formants, and the particular characteristics in sound structure were shown to vary according to the vocalization conditions and the situations, and where the animals were placed, even within the same call types. [source] Anti-Predator Signals as Advertisements: Evidence in White-Throated Magpie-JaysETHOLOGY, Issue 6 2009Jesse M. S. Ellis Calls and displays elicited by predators usually function as alarms or to inform predators of their detection. However, predator encounters may afford some individuals the opportunity to demonstrate quality or signal their availability. Here, I report on a class of vocal signals produced in predator-elicited displays that share many characteristics with sexually selected song. White-throated magpie-jays (Calocitta formosa) display at low-threat predators while producing ,loud display calls' (LDCs). I use this term because the calls occur primarily in two display contexts (see below) though occasionally in other contexts as well. Such calls and displays are primarily produced by males, and also occur in one other context, at dawn. Playback experiments showed that despite being elicited by predators, males were more likely than females to respond to LDCs, and more likely to respond when their mate was fertile. Over 134 different call types were produced in over 200 displays by 34 males; the largest minimum repertoire size was 67. Presentations of taxidermic raptor mounts elicited some LDCs, but fewer calls and lower diversity than at dawn or in predator approach displays. The male bias and high diversity suggest that LDCs are an outcome of intersexual selection, while their elicitation by predators suggests an alarm function. I propose that male magpie-jays use predator encounters as opportunities to advertise their presence and availability as mates; they use LDCs as songs. Such a communication system seems to have been favored by the unusual social system of magpie-jays, in which female groups defend territories and males have little opportunity to defend resources for mate attraction, forcing them to advertise when females are paying the most attention, during predator encounters. [source] Semantic Differences in Sifaka (Propithecus verreauxi) Alarm Calls: A Reflection of Genetic or Cultural Variants?ETHOLOGY, Issue 9 2006Claudia Fichtel In this study, we compared the usage of alarm calls and anti-predator strategies between a captive and a wild lemur population. The wild lemur population was studied earlier in Western Madagascar (Fichtel & Kappeler 2002). The captive population was studied in outdoor enclosures of the Duke University Primate Center. Alarm calls and anti-predator behavior were elicited by conducting experiments with both vocal and visual dummies. We scored the subjects' immediate behavioral responses, including alarm calls, from video recordings made during the experiments. In principle, both populations have a mixed alarm call system with functionally referential alarm calls for aerial predators and general alarm calls for terrestrial and aerial predators and for situations associated with high arousal, such as group encounters. Although wild and captive sifakas exhibit the same alarm call system and use the same alarm call types, we discovered striking differences in the usage and perception of some of the alarm calls. We argue that these differences indicate either an evolutionary drift in the meaning of these calls or reflect cultural variation. The latter possibility is consistent with our understanding of the ontogeny of call usage and comprehension. [source] Acoustic Features of Female Chacma Baboon BarksETHOLOGY, Issue 1 2001Julia Fischer We studied variation in the loud barks of free-ranging female chacma baboons (Papio cynocephalus ursinus) with respect to context, predator type, and individuality over an 18-month period in the Moremi Game Reserve, Botswana. To examine acoustic differences in relation to these variables, we extracted a suite of acoustic parameters from digitized calls and applied discriminant function analyses. The barks constitute a graded continuum, ranging from a tonal, harmonically rich call into a call with a more noisy, harsh structure. Tonal barks are typically given when the signaler is at risk of losing contact with the group or when a mother and infant have become separated (contact barks). The harsher variants are given in response to large predators (alarm barks). However, there are also intermediate forms between the two subtypes which may occur in both situations. This finding is not due to an overlap of individuals' distinct distributions but can be replicated within individuals. Within the alarm bark category, there are significant differences between calls given in response to mammalian carnivores and those given in response to crocodiles. Again, there are intermediate variants. Both alarm call types are equally different from contact barks, indicating that the calls vary along different dimensions. Finally, there are consistent, significant differences among different individuals' calls. However, individual identity in one call type cannot directly be inferred from knowledge of the individuals' call characteristics in the other. In sum, the barks of female baboons potentially provide rich information to the recipients of these signals. The extent to which baboons discriminate between alarm and contact barks, and classify calls according to context and/or acoustic similarity will be described in a subsequent paper. [source] Changes In Rhesus Macaque ,Coo' Vocalizations during Early DevelopmentETHOLOGY, Issue 10 2000Kurt Hammerschmidt In order to test whether ,coo' calls of young rhesus macaques, Macaca mulatta, undergo some modifications during early development, and to explore which factors may influence these changes, we studied the ontogeny of their contact call, the ,coo' call. Vocalizations were recorded during brief periods of social separation. Infants were either raised with their mothers and other conspecifics, or separated from their mothers at birth and housed in a nursery with other infants. We recorded calls uttered in the separation context from 20 infants. We digitized the first 50 calls of a given series and subjected them to a Fourier transform. From each frequency,time spectrum, we extracted 65 acoustic parameters using a software program (LMA 5.9). We then used a cluster analysis to separate the ,coo' calls from other call types. With increasing age, the ,coos' dropped in pitch and became more even. The course of amplitude became more constant and the call duration increased slightly. Nevertheless, we found a high intra-individual variation throughout the 5 mo. Neither rearing condition nor sex had any apparent influence on age-related changes in ,coo' structure. With one exception, all parameters that correlated with age could be explained by variation in weight. Therefore, we conclude that growth is the main factor accounting for the observed changes. [source] Fusion of dispatching centres into one entity: effects on performanceACTA ANAESTHESIOLOGICA SCANDINAVICA, Issue 6 2010T. MÄÄTTÄ Background: Dispatching centres were fused into one of the 112 entity, which caused concerns regarding whether the medical calls could be processed effectively also in the new centre. We evaluated the effects of the reform on key performance criteria in medical calls. Methods: This observational study in the Helsinki Dispatching Centre consisted of two periods: Period I 2 years before the reform and Period II 2 years after. The main outcome measures were answering and call processing times, accuracy of risk assessment and appropriate use of ambulances. Results: In Period I (n=574,276), 92.2% of all incoming phone calls were answered within 10 s and in Period II (n=758,022) 82.8% (P<0.0001). Time to dispatch a first responding fire unit increased from 98 to 113 s (P<0.0001) and an advanced life support unit in category A calls increased from 73 to 84 s (P<0.0001). In Period I 47.7%, 34.8% and 17.5% of phone calls were completed in <3, 3,5 and >5 min and in Period II 29.8%, 36.1% and 34.1% (P<0.0001). The number of three studied non-transportation call types and unnecessary lights-and-siren responses increased significantly (P<0.0001 and 0.0001, respectively). Neither the accuracy of risk assessment in the three studied call types nor the rate of telephone-guided cardiopulmonary resuscitation changed. Conclusions: The reform increased the total number of ambulance dispatches, prolonged answering and call processing times and had a negative effect on the appropriate use of ambulances. The accuracy of risk assessment was not affected. Evidence-based data should be the basis for the future as dispatching centre processes are shown to be vulnerable during organisational reforms. [source] Sex differences in the vocal repertoire of adult red-capped mangabeys (Cercocebus torquatus): a multi-level acoustic analysisAMERICAN JOURNAL OF PRIMATOLOGY, Issue 4 2010Hélène Bouchet Abstract Sex differences in the vocal behavior of nonhuman primates can take various forms: sex-specific call types, differential production of shared call types, or sex discrepancy in phonation. Also, a growing literature is evidencing that systematically analyzing the vocal repertoires of primates at the call level might lead to underestimating their communicative abilities. Here, we present an extensive multi-level analysis of the still unknown vocal repertoire of adult red-capped mangabeys (Cercocebus torquatus), with a special emphasis on sex differences. We collected recordings from seven adult males and seven adult females housed in captivity. We present a structurally-based classification of mangabey calls that we cross-validated by an analysis of the associated contexts of emission. We found 12 sound units (including six sex-specific) that were concatenated to form eight call types (including four sex-specific), which were produced either singularly or in sequences composed of one ("repetition") or several ("combination") call types. We extracted organizational principles that ruled call composition and calling patterns. This revealed a high degree of potentially meaningful variability in terms of semantics and syntax. Male,female discrepancy in terms of phonation could be related to morphological dimorphism and would enable listeners to behave appropriately according to the sex of the caller. Sex differences in repertoire size, structural gradation, and call usage could reflect specificities of male,female social roles. We discuss the pertinence of these sex differences according to social system and habitat quality. Am. J. Primatol. 72:360,375, 2010. © 2010 Wiley-Liss, Inc. [source] Production and perception of sex differences in vocalizations of Wied's black-tufted-ear marmosets (Callithrix kuhlii)AMERICAN JOURNAL OF PRIMATOLOGY, Issue 4 2009Adam S. Smith Abstract Males and females from many species produce distinct acoustic variations of functionally identical call types. Social behavior may be primed by sex-specific variation in acoustic features of calls. We present a series of acoustic analyses and playback experiments as methods for investigating this subject. Acoustic parameters of phee calls produced by Wied's black-tufted-ear marmosets (Callithrix kuhlii) were analyzed for sex differences. Discriminant function analyses showed that calls contained sufficient acoustic variation to predict the sex of the caller. Several frequency variables differed significantly between the sexes. Natural and synthesized calls were presented to male,female pairs. Calls elicited differential behavioral responses based on the sex of the caller. Marmosets became significantly more vigilant following the playback of male phee calls (both natural and synthetic) than following female phee calls. In a second playback experiment, synthesized calls were modified by independently manipulating three parameters that were known to differ between the sexes (low-, peak-, and end-frequency). When end-frequency-modified calls were presented, responsiveness was differentiable by sex of caller but did not differ from responses to natural calls. This suggests that marmosets did not use end-frequency to determine the sex of the caller. Manipulation of peak-and low-frequency parameters eliminated the discrete behavioral responses to male and female calls. Together, these parameters may be important features that encode for the sex-specific signal. Recognition of sex by acoustic cues seems to be a multivariate process that depends on the congruency of acoustic features. Am. J. Primatol. 71:324,332, 2009. © 2008 Wiley-Liss, Inc. [source] Geographic variation in loud calls of sportive lemurs (Lepilemur ssp.) and their implications for conservationAMERICAN JOURNAL OF PRIMATOLOGY, Issue 9 2008Maria Méndez-Cárdenas Abstract Bioacoustical studies in nonhuman primates have shown that loud calls can be reliably used as a noninvasive diagnostic tool for discriminating cryptic taxa, for their monitoring in the field as well as for the reconstruction of their phylogeny. To date, it is unknown, whether loud calls can be used for these purposes in sportive lemurs, for which current genetic studies suggest the existence of at least 24 cryptic species. The aim of this study was to compare the structure of loud calls of populations of sportive lemurs to characterize informative acoustic traits for taxa discrimination and to establish a phylogenetic tree based on acoustic structure. We have based our study on Inter-River-Systems (IRSs) as operational taxonomic units. Samples were collected from nine different localities of four IRSs along a transect from northwestern to northern Madagascar. Two call types, the ouah and the high-pitched call, were present in almost all IRSs. Six temporal and eight spectral parameters were measured in 196 calls of the best quality given by 21 different males. Variation within and between IRSs was assessed by multivariate statistics. Loud calls differed significantly among the different IRSs. The IRSs varied most in spectral parameters, whereas temporal parameters were less variable. Phylogenetic analysis using parsimony yielded 11 out of 17 acoustic characters as phylogenetically informative. The acoustic tree had an average branch support of 78%. Its topology coincided less with geographic distances than with genetic tree topology. Altogether our findings revealed that loud calls separated geographically isolated populations of sportive lemurs specifically. Based on these results, noninvasive tools for diagnosis and monitoring of cryptic species in nature can be developed for conservation management. Am. J. Primatol. 70:828,838, 2008. © 2008 Wiley-Liss, Inc. [source] The structure of vocalization of ewes and male lambs at pastureANIMAL SCIENCE JOURNAL, Issue 1 2009Hirofumi NAEKAWA ABSTRACT We performed an analysis of the vocalization of 161 ewes and 50 male lambs that were pastured day and night. The vocalization structures of the phonetic notations of the opened-mouth from closed mouth /,aee/ and /,naeee/ and closed-mouth /,,,,/ of ewes, and the opened-mouth from closed-mouth /,eee/ and /,neeee/ and closed-mouth /,,,,/ of male lambs were studied in terms of their audio characteristics. The items subject to analysis included duration of each vocalization, fundamental frequency, sound pressure and first formant (F1), second formant (F2), and third formant (F3). Among the male lambs, the duration of each call type showed significant differences depending on the behavior types or the target types, and the closed-mouth to open-mouth sounds, /,eee/ and /,neeee/ showed a tendency to be longer than the closed-mouth sound of /,,,,/. A significant correlation (r = 0.9, P < 0.05) was observed between the fundamental frequency and F1 with the /,eee/ type of call of the male lambs when the vocalization was targeted toward the stockperson. When the ewes' behavior pattern was grazing and moving and the calling target was an ewe, the sound pressure significantly differed between /,,,,/ and /,naeee/ (P < 0.05). From the analysis of the call durations, the fundamental frequencies, the sound pressures and formants, and the particular characteristics in sound structure were shown to vary according to the vocalization conditions and the situations, and where the animals were placed, even within the same call types. [source] The "Vertical Response Time": Barriers to Ambulance Response in an Urban AreaACADEMIC EMERGENCY MEDICINE, Issue 9 2007Robert A. Silverman MD Background: Ambulance response time is typically reported as the time interval from call dispatch to arrival on-scene. However, the often unmeasured "vertical response time" from arrival on-scene to arrival at the patient's side may be substantial, particularly in urban areas with high-rise buildings or other barriers to access. Objectives: To measure the time interval from arrival on-scene to the patient in a large metropolitan area and to identify barriers to emergency medical services arrival. Methods: This was a prospective observational study of response times for high-priority call types in the New York City 9-1-1 emergency medical services system. Research assistants riding with paramedics enrolled a convenience sample of calls between 2001 and 2003. Results: A total of 449 paramedic calls were included, with a median time from call dispatch to arrival on-scene of 5.2 minutes. The median on-scene to patient arrival interval was 2.1 minutes, leading to an actual response interval (dispatch to patient) of 7.6 minutes. The median on-scene to patient interval was 2.8 minutes for residential buildings, 2.7 minutes for office complexes, 1.3 minutes for private homes (less than four stories), and 0.5 minutes for outdoor calls. Overall, for all calls, the on-scene to patient interval accounted for 28% of the actual response interval. When an on-scene escort provided assistance in locating and reaching the patient, the on-scene to patient interval decreased from 2.3 to 1.9 minutes. The total dispatch to patient arrival interval was less than 4 minutes in 8.7%, less than 6 minutes in 28.5%, and less than 8 minutes in 55.7% of calls. Conclusions: The time from arrival on-scene to the patient's side is an important component of overall response time in large urban areas, particularly in multistory buildings. [source] |