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Collaborative Research
Lone Pine Koala Sanctuary is dedicated to the research of native species and continues to collaborate with Universities and the Government. This page highlights some of the papers published resulting from these efforts. For more information on this or other research, e-mail us at
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Johnston, S. D., O'Callaghan, P, Nilsson, K, Tzipori, G., Strong, H. and Curlewis, J. D. (2003). Semen-induced luteal phase in the koala. In: Martin and G.B., Reproduction, Fertility and Development. Society for Reproductive Biology Thirty-fourth Annual Conference, Melbourne, Victoria, (92-92). 14-17 September 2003. Abstract: The koala ovulates in response to mating. The purpose of this study was to document the LH surge induced by copulation and to investigate the potential roles of mechanical stimulation of the urogenital sinus and deposition of semen in induction of the luteal phase. In experiment 1, serial blood samples from four koalas that underwent normal mating showed elevated concentrations of LH approximately 24-32 h post-coitus. There was no corresponding elevation in LH in koalas (n = 4) that were exposed to the presence of a male but received no physical contact. In experiment 2, koalas on day 2 of oestrus were exposed to one of the following treatments (n = 9 per group): artificial insemination with 1 ml 0.9% sterile saline (control group), insemination with 1 ml koala semen, stimulation of the urogenital sinus with a purpose built glass rod (designed to mimic the action of the penis during natural mating) and urogenital stimulation with the glass rod followed by insemination of 1 ml koala semen. Confirmation of a luteal phase was based on evidence of a prolonged return to oestrus, parturition and/or elevated progesterone concentrations. Insemination of saline (0/9) and urogenital stimulation (0/9) failed to induce a luteal phase. Insemination of semen without glass rod stimulation resulted in a luteal phase in 4/9 koalas, three of which gave birth. Insemination of semen in combination with urogenital stimulation produced a luteal phase in 7/9 koalas, four of which gave birth. Semen had a significant effect on induction of the koala luteal phase (P < 0.001) but glass rod stimulation had no such effect (P = 0.335). It was concluded that semen must be involved in the induction of a luteal phase in the koala. The results presented in this study will serve to improve optimal timing and induction of ovulation for artificial insemination in the koala. Johnston, S. D., Mcgowan, M. R., O'Callaghan, P., Cox, R. and Nicholson, V. (2000) Natural and artificial methods for inducing the luteal phase in the koala (Phascolarctos cinereus). Journal of Reproduction and Fertility, 120 1: 59-64. Abstract: An experiment was conducted in which female koalas were mated for different durations of intromission and ejaculation to confirm that the luteal phase of the oestrous cycle in koalas is induced by the physical act of mating. Results showed that induction of a luteal phase in the koala usually required a complete duration of penile thrusting behaviour from the male. It is proposed that induction of a luteal phase in koalas may involve a copuloceptive reflex, triggered by the thrusting of the male's penis into the female's urogenital sinus. Although interrupted mating in koalas may be used to induce a luteal phase in preparation for an artificial insemination programme, this study showed that there is a 12.5% probability that pregnancy will result from semen prematurely emitted by the teaser male. A dose of 250 iu hCG was administered intramuscularly to eight oestrous females to determine whether it was possible to induce a luteal phase artificially. In contrast to control females, which received sterile saline injections, all females injected with hCG showed a significant increase in progestogen concentration, above that of basal values, indicating that a luteal phase had been induced successfully.
Abstract: As an integral part of the development of an artificial insemination programme in the captive koala, female reproductive physiology and behaviour were studied. The oestrous cycle in non-mated and mated koalas was characterized by means of behavioural oestrus, morphology of external genitalia and changes in the peripheral plasma concentrations of oestradiol and progestogen. The mean (:!: SEM) duration of the non-mated oestrous cycle and duration of oestrus in 12 koalas was 32.9 :!: 1.1 (n = 22) and 10.3 :!: 0.9 (n = 24) days, respectively. Although the commencement of oestrous behaviour was associated with increasing or high concentrations of oestradiol, there were no consistent changes in the morphology or appearance of the clitoris, pericloacal region, pouch or mammary teats that could be used to characterize the non-mated cycle. As progestogen concentrations remained at basal values throughout the interoestrous period, non-mated cycles were considered non-luteal and presumed anovulatory. After mating of the 12 koalas, six females gave birth with a mean (:!: SEM) gestation of 34.8 :!: 0.3 days, whereas the remaining six non-parturient females returned to oestrus 49.5:!: 1.0 days later. After mating, oestrous behaviour ceased and the progestogen profile showed a significant increase in both pregnant and non-parturient females, indicating that a luteal phase had been induced by the physical act of mating. Progestogen concentrations throughout the luteal phase of the pregnant females were significantly higher than those of non-parturient females. Parturition was associated with a decreasing concentration of progestogen, which was increased above that of basal concentrations until 7 days post partum. Wardrop, S., Fowler, A., O'Callaghan, P., Giffard, P., and Timms, T. (1999) Characterization of the koala biovar of Chlamydia pneumoniae at four gene loci--ompAVD4, ompB, 16S rRNA, groESL spacer region. Systematic and Applied Microbiology, 22 1: 22-27. Abstract: Koalas are infected with two species of Chlamydia, C. pecorum and C. pneumoniae. While it is known that significant genetic diversity occurs in the C. pecorum strains infecting koalas, very little is known about the C. pneumoniae strains that infect this host. In the current study, 10 isolates of koala C. pneumoniae were analysed at four gene loci and found to be different to both the human and horse C. pneumoniae strains at all loci (biovar differences ranging from 0.3% at groESL up to 9.0% at ompAVD4). All koala biovar isolates studied were found to be 100% identical at ompAVD4 (all 10 isolates) and at ompB (all three isolates) genes. This lack of allelic polymorphisms at ompAVD4 has now been observed for koala C. pneumoniae, human C. pneumoniae, guinea pig inclusion conjunctivitis C. psittaci and feline conjunctivitis C. psittaci and may be correlated to a lack of antibody response to the chlamydial major outer membrane protein (MOMP) in these same strain/host combinations. This study also provides the first documented case of natural C. pneumoniae infection causing a severe and extended respiratory episode in a captive koala population. This captive episode is in contrast to most free-range observations in which koala C. pneumoniae is rarely documented as causing respiratory, ocular or urogenital tract disease. Memoirs of the Queensland Museum 33. (1993) A Record of Communal Egg Laying in the Skink Carlia Tetradactyla (Reptilia: Scincidae).
Porter, R. (1993) An observation of insectivorous feeding habits in the green tree snake (Dendrelaphis punctulata), Herptofauna, 23 1:36. Abstract: During a recent visit to Carnarvon Gorge, central Queensland, a brief observation was made of an unusual feeding behaviour in the colubrid snake Dendrelaphis punctulata. At around 1100 hours on a warm sunny day (temperature approximately 28°C) in early March 1993, a green tree snake was seen amongst a clump of sedge grass approximately 1 metre from the river's edge. The snake appeared active and quite agitated, moving nervously in a short "start stop" motion while holding an object in its jaws. On closer inspection the item was seen to be some type of flying insect as a pair of large, elliptical, transparent wings were projecting out of each side of the mouth. The wings were consistent with a dragon -or damsel-fly, a lace wing or a similar type of insect. The wings were seen to move up and down slightly, though this appeared to be a consequence of the snake making a chewing motion rather than movement from the insect. When approached closer the snake rapidly fled into the clump of sedge and disappeared. Many early authors listed insects as prey items for Australian snakes (e.g. Kinghorn, 1929, Worrell, 1963, Gow, 1976). However, Shine (1991 a) states that although insect fragments are often found in snake digestive tracts, in most cases these were secondarily ingested from a vertebrate prey item. He does indicate that occasional crickets have been found in some elapids and in his examination of Australian colubrids (Shine, 1991 b) he lists 76 prey items from 58 D. punctulata, including one insect item, also a cricket. Considering the huge number of Australian snake stomach contents examined by Shine over the last 15 years the occurrence of insects as prey items in Australian snakes (apart from typhlopids) is evidently a very rare event. It is possible that the insect observed being eaten by the green tree snake had been captured by a frog or lizard which was then taken by the snake, both items being swallowed consecutively. It seems likely however, that the frog or lizard would have dropped the prey item when the snake struck. Even if this did occur, the insect may have become contaminated by the lizard or frog's scent (in the same fashion as keepers scent mice for lizard eating snakes) and the insect then eaten independently by the snake. The most parsimonious explanation, however, has to be that the snake captured and ate the insect itself, despite the rarity of such events in Australian snakes. Though the importance of invertebrates in most native snake diets is apparently negligible, this observation still raises some interesting questions regarding the causes of such behaviour. Osawa, R. and Walsh, T. P. (1993) Effects of Acidic and Alkaline Treatments on Tannic Acid and its Binding Property to Protein. Journal of Agricultural and Food Chemistry, 41 5: 704-707. Abstract: Effects of acidic and alkaline treatments on tannic acid (T A), one of the hydrolyzable tannins, and its binding property to protein [bovine serum albumin (BSA)] were investigated. Dissociation of TA-BSA complexes was apparent in both highly acidic (pH <3) and alkaline (pH >7) treatments. T A dissociated from the complexes and pure T A was not significantly hydrolyzed in highly acidic (pH 1.0-3.0) media and-retained its protein-binding property. TA did not seem to be hydrolyzed even with a more acidic treatment (in 1 M HCI, pH <0.5), although its protein-binding property was much reduced. The higher pH treatment (pH >6.-5) facilitated the hydrolysis of T A, as judged by the release of its constituent Gallic acid. Osawa, R., Walsh, T.P., Cork, S. J. (1993) Metabolism of tannin-protein complex by facultatively anaerobic bacteria isolated from koala faeces. Biodegradation, 4 2: 91-99. Abstract: The metabolic pathways involved in degradation of tannin-protein complex (T-PC) were investigated in various facultatively anaerobic bacteria, with specific reference to faecal isolates from the koala including T -PCdegrading enterobacteria (T -PCDE), Streptococcus bovis, Klebsiellapneumoniae, and K. oxytoca. It was demonstrated that ~-PCDE and S. bovis biotype I were capable of degrading protein complexed with Gallo tannin (a hydrolyzable tannin), but not that complexed with quebracho (a condensed tannin). Subsequent studies showed that these strains metabolized Gallic acid to pyrogallol. Strains of Klebsiella pneumoniae and K. oxytoca, which did not degrade T -PC, also metabolized Gallic acid into pyrogallol. Pyrogallol was not degraded by any strains studied, but it was not detected in fresh faeces of the koalas. The majority of strains isolated from faeces could degrade phloroglucinol. Based on these findings, we propose that members of the gut microflora of the koala cooperate in the degradation of T -PC.
Abstract: Quantitative and qualitative studies on the micro flora in the faeces of 10 female koalas, Phascolarctos cinereus, were conducted with specific reference to 'pap', a special maternal faeces consumed by the juvenile at about the time of first emergence from the pouch. This specific coprophagy, called 'pap feeding', occurred multiple times in all of the females examined. Pap was higher in water content (81.8%) and pH (7.0) than normal faeces produced by the females before and after pap feeding (54.6-56.4% and 5.5, respectively), suggesting that it is derived directly from the contents of the caecum. Pap had higher (23-41-fold) viable counts of tannin-protein-complex-degradi enterobacteria (T -PCDE) than the normal faeces; in four of the females examined, viable T -PCDE were found in pap but never in the normal faeces. The evidence indicates that pap feeding is an essential physiological activity for the juvenile koala to prepare it for an imminent dietary transition from maternal milk to tannin-rich eucalypt leaves.
Abstract: Tannase activity of bacteria capable of degrading tannin-protein complexes was determined by a newly developed visual reading method. The method is based on two phenomena: (i) the ability of tannase to hydrolyze methyl gallate to release free Gallic acid and (ii) the green to brown coloration of Gallic acid after prolonged exposure to oxygen in an alkaline condition. The method has been successfully used to detect the presence of tannase in the cultures of bacteria capable of degrading tannin-protein complexes. Osawa, R. and Woodall, P. F. (1992) A Comparative Study of Macroscopic and Microscopic Dimensions of the Intestine in Five Macropods (Marsupialia: Macropodidae). I. Allometric Relationships. Australian Journal of Zoology, 40 1: 91-98. Abstract: Macroscopic and microscopic dimensions of the intestines in five macropod species (the red kangaroo, Macropus rufus; the eastern grey kangaroo, M. giganteus; the agile wallaby, M. agilis; the swamp wallaby, Wallabia bicolor; and the red-necked pademelon, Thylogale thetis) were investigated allometrically in relation to body mass. In general, the length of the small intestine changed in an area: volume (A: V) compensating manner, but the circumference showed negative allometry such that the overall change in surface areas, both ground and mucosal (including the contribution of villi), were isometric but also included the coefficient derived from 'Kleiber's Law' (0' 75) in their 95 and 99% confidence limits, respectively. Villous height and width generally showed no significant correlations with body size, but villous density was lower in large individuals. The allometry coefficient for the length of the large intestine was generally near the A: V compensating value (0' 5) in most intraspecific analyses but much higher in the interspecific analysis, suggesting that some factor other than body size might be important (possibly dietary fibre). Caecal length was significantly correlated with body size only in two largest species (M. rufus and M. giganteus) and the interspecific analysis gave a value near A: V compensation). Osawa, R. O., Fujisa, T. and Mitsuoka, T. (1992) Characterization of Gram-negative anaerobic strains, isolated from koala feces, which exhibit satellite growth and pleomorphism. Systematic and Applied Microbiology, 15 4: 628-635. Abstract: Three strains, which showed satellite growth around colonies of concomitant isolates of Escherichia coli, were isolated from koala feces. Experimental inoculation of these strains and E. coli strains on a plate medium anaerobic, gram-negative, and highly pleomorphic rods. They were bile resistant and asac-charolytic, and produced only a trace amount of propionic acid from peptone yeast-extract Fildes-solution with glucose broth. Their growth was stimulated by succinic acid but completely inhibited by fumaric acid. Subsequent biochemical analysis revealed that the strains produced a large amount of propionic acid from peptone yeast-extract (PY) broth supplemented with sodium succinate. A PY broth agar plate, which contained 30% E. coli-metabolized PY broth, enhanced growth of the strains, and it was found that this spent broth contained succinic acid produced by the E. coli. The evidence suggests that the observed satellite growth was due to succinic acid produced by E. coli strains. Osawa, R., Blanshard, W. H. and O'Callaghan, P. G. (1992) Microflora of the Pouch of the Koala (Phascolarctos cinereus). Journal of Wildlife Diseases, 28 2: 276-280. Abstract: Microflora of the pouch epithelium of 17 female koalas (Phascolarctos cinereus) were examined in relation to their current reproductive status and recent reproductive history. No microbial growth was observed in pouch swabs from 13 of 17 (76%) koalas, including four females without young, seven with pouch young and two with back young (i.e. permanently emerged from the pouch). Growth of bacteria or yeasts was observed in pouch swabs from four koalas, each of which had experienced mortality of its pouch young during the current breeding season. Seven species of micro-organisms were isolated, including Pseudomonas aeruginosa, Serratia marcescens and Enterococcus faecalis. Based on the absence of microflora in the majority of females examined, we propose that the pouch epithelium normally provides a hostile environment for microbial colonization. Osawa, R. (1992) Tannin-Protein Complex-Degrading Enterobacteria Isolated from the Alimentary Tracts of Koalas and a Selective Medium for Their Enumeration. Applied Environmental Microbiology, 58 5: 1754-1759. Abstract: Tannin-protein complex (T -PC)-degrading enterobacteria (T -PCDE) were isolated from the feces and from a layer of bacteria attached to the cecal wall of koalas. The T -PCDE were facultatively anaerobic, gram-negative, pleomorphic, nonmotile bacilli. The bacteria were also oxidase and catalase negative and resistant to vancomycin, reduced nitrates to nitrites, and grew on MacConkey agar. Growth on tannin-treated agar media showed a distinctive clear zone around the colony. From these observations, a selective agar plate medium (vancomycin- and tannin-treated Wilkins-Chalgren anaerobe. agar) was developed to enumerate T-PCDE isolated from the feces of koalas. This medium was highly selective in the enumeration of the fecal T -PCDE and inhibited the growth of concomitant T -PC-degrading Streptococcus bovis. The T -PCDE were isolated from 10 of the 12 captive koalas studied; in 8 of these 10 koalas, the facultatively anaerobic bacterial flora was dominated (more than 60%) by T-PCDE. Viable numbers of T-PCDE were, in most of the animals, much larger (more than 100 times) than the numbers of T -PC-degrading S. bovis, suggesting that T -PCDE played a more active role in digesting T -PC in the alimentary tracts of koalas. Porter, R. The Current Status of the Knob-tailed Geckos (Nephrurus) in captivity.
Osawa, R. and Sly, L. I. (1991) Phenotypic Characterization of CO2-Requiring Strains of Streptococcus bovis from koalas. Applied Environmental Microbiology, 57 10: 3037-3039.
Porter, R. (1991) Unusual Basking Behaviour in captive bearded dragons (Pongona barbata). Herpetofauna, 21 2:31. Osawa, R., Carrick, F.N., Hashimoto, N., Takashima, I. and Takahasi, T. (1991) Application of a Blood Sampling Paper Method for Complement Fixation Test Detection of Anti- Chlamydial Antibody in Koalas, Phascolarctos cinereus. In Biology of the Koala. (Eds. Lee, A.K, Handasyde, K.A. and Sanson, G.D. ) pp. 97-108.
Blanshard, W. H. (1991) Growth and development of the koala from birth to weaning. In Biology of the Koala. (Eds. Lee, A.K., Handasyde, K.A. and Sanson, G.D.) pp. 193-202.
Osawa, R. and Woodall, P. F. (1990) Feeding Strategies of the Swamp Wallaby, Wallabia-Bicolor, on North Stradbroke Island, Queensland .2. Effects of Seasonal-Changes in Diet Quality on Intestinal Morphology. Wildlife Research Management and Conservation, 17 6: 623-632.
Osawa, R. (1990) Feeding Strategies of the Swamp Wallaby, Wallabia bicolor, on North Stradbroke Island, Queensland. I: Composition of Diets. Wildlife Research Management and Conservation, 17 6: 615-621. Osawa, R. (1990) Formation of a Clear Zone on Tannin-Treated Brain Heart Infusion Agar by a Streptococcus sp. Isolated from Feces of Koalas. Applied Environmental Microbiology, 56 3: 829-831.
Osawa, R. and Mitsuoka, T. (1990) Selective Medium for Enumeration of Tannin-Protein Complex Degrading-Streptococcus spp. in Feces of Koalas. Applied Environmental Microbiology, 56 11: 3609-3611. Osawa, R. and Carrick, F. N. (1990) Use of a dietary supplement in koalas during systemic antibiotic treatment of chlamydial infection. Australian Veterinary Journal, 67 8: 305-307. Osawa, R. and Mitsuoka, T. (1990) Faecal microflora of captive koalas, Phascolarctos cinereus (Marsupialia: Phascolarctidae). Australian Mammalogy 13: 141-147.
Osawa, R. (1989) Road-kills of the Swamp Wallaby, Wallabia bicolor, on North Stradbroke Island, South-east Queensland. Wildlife Research Management and Conservation, 16 1: 95-104.
Perception of Male Caller Identity in Koalas (Experiments Phascolarctos cinereus Acoustic Analysis and Playback Experiments
Benjamin D. Charlton1*, William A. H. Ellis2, Allan J. McKinnon3, Jacqui Brumm4, Karen Nilsson4, W. Tecumseh Fitch1 1 Department of Cognitive Biology, University of Vienna, Vienna, Austria, 2 Koala Ecology Group, School of Biological Sciences, University of Queensland, Brisbane, Queensland, Australia, 3 Department of Environment and Resource Management, Moggill Koala Hospital, Bellbowrie, Queensland, Australia, 4 Lone Pine Koala Sanctuary, Brisbane, Queensland, Australia
Abstract
The ability to signal individual identity using vocal signals and distinguish between conspecifics based on vocal cues is important in several mammal species. Furthermore, it can be important for receivers to differentiate between callers in reproductive contexts. In this study, we used acoustic analyses to determine whether male koala bellows are individually distinctive and to investigate the relative importance of different acoustic features for coding individuality. We then used a habituation-discrimination paradigm to investigate whether koalas discriminate between the bellow vocalisations of different male callers. Our results show that male koala bellows are highly individualized, and indicate that cues related to vocal tract filtering contribute the most to vocal identity. In addition, we found that male and female koalas habituated to the bellows of a specific male showed a significant dishabituation when they were presented with bellows from a novel male. The significant reduction in behavioural response to a final rehabituation playback shows this was not a chance rebound in response levels. Our findings indicate that male koala bellows are highly individually distinctive and that the identity of male callers is functionally relevant to male and female koalas during the breeding season. We go on to discuss the biological relevance of signalling identity in this species’ sexual communication and the potential practical implications of our findings for acoustic monitoring of male population levels. Charlton BD, Ellis WAH, McKinnon AJ, Brumm J, Nilsson K, et al. (2011) Perception of Male Caller Identity in Koalas (Phascolarctos cinereus): AcousticCitation:
Analysis and Playback Experiments. PLoS ONE 6(5): e20329. doi:10.1371/journal.pone.0020329 Editor: Nicolas Mathevon, University of Saint-Etienne, France Received March 16, 2011; Accepted April 21, 2011; Published
May 25, 2011 Copyright: ! 2011 Charlton et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits
unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Funding: B.D. Charlton was supported by a European Research Council Advanced Grant SOMACCA (No. 230604) awarded to W. Tecumseh Fitch. The funders had
no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Competing Interests:
The authors have declared that no competing interests exist.
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Introduction Individually distinctive vocal signals and the ability to discriminate between individuals based on their vocalizations are documented in several mammal species ([1–3], for review see [4]). Indeed, we would expect signallers to be individually distinctive and receivers to differentiate between individuals where it is adaptive for them to do so [5]. For example, in social mammals individually distinctive vocalizations may be important for facilitating group cohesion [6,7] recognizing kin [8] and warning group members of potential danger [9,10]. In addition, mother offspring vocal recognition can be crucial for dependant young to survive [11–13]. However, vocal recognition and the ability to signal individual identity may also be important in inter and intra-sexual contexts. For instance, individually distinctive calls are important for delineating territories [14,15] and the ability to distinguish between unfamiliar and familiar rivals could help prevent unnecessary contests between males [16]. In addition, over the course of a breeding season, females may become familiar with and prefer the vocalisations of certain males that can afford higher energy courtship displays [17–19]. Koalas ( determines the fundamental frequency (F0) of the vocalization and the supra-laryngeal vocal tract acts as a spectral filter, selectively transmitting certain frequencies termed vocal tract resonances or ‘formants’ [27]. Since inter-individual differences in laryngeal and vocal tract morphology are likely, both source and filter-related acoustic characteristics of male koala bellows have the potential to yield information on the caller’s identity. In addition, the very low F0 of male bellows should highlight an individual’s distinctive formant pattern, making these calls particularly well suited for identity cueing (as discussed by [28]). Furthermore, although male bellowing occurs in response to other male bellows and after agonistic interactions or mating attempts [23], ‘spontaneous’ bellows often occur just after males have moved to a new location [20]. Although we cannot rule out the stimulating affects of olfactory signals, this may indicate that is important for males to advertise their presence to neighbouring conspecifics, and perhaps a more general broadcasting function for this call. In addition, koalas occupy overlapping ranges and roam more widely during the breeding season [22,29]. Consequently, they will interact with others in adjacent territories more at this time and could familiarize themselves with the bellows of certain individuals. The perception of caller identity might prove adaptive in this species, allowing female koalas to exhibit mating preferences based on familiarity and male koalas to avoid known rivals that represent a threat to them. For this to occur, however, male koalas need to possess individually distinctive bellows, and male and female koalas need to distinguish between the calls of different males. Here we use acoustic analyses based on source-filter theory to determine whether male koala bellows are individually distinctive vocalizations, and to assess the relative importance of different source- and filter-related acoustic features for coding individuality. We then use a habituation-discrimination paradigm [3,30–34] to investigate whether male and female koalas can perceive differences between male callers. We predict that after habituating to a series of male bellows, both sexes will show a renewal of response levels to a bellow from a novel male. Such perceptual abilities could be adaptive in the contexts of intra-sexual competition and mate choice, and would raise further questions about the possible functions of identity cueing in koala sexual communication.
Results Description of male bellows Male koala bellows typically begin with a ‘staccato’ introductory phase that consists of abrupt amplitude onsets and offsets and no
clear harmonic structure. This is followed by a continuous series of inhalations and shorter ‘belch-like’ exhalations (see Figure 1a and
Movie S1). The inhalation phases of male bellows have a very low F0 (circa 25 Hz), making a pulse-train structure visible in the spectrograms (see Figure 1b). The pulses presumably represent glottal closure and the rate that they occur per second determines the F0 of these sections of the vocalisation. In addition, clear spectral prominences are present during the inhalation, and initial exhalation, phases of bellows that are likely to represent supralaryngeal resonances (see Figure 1b). We only considered the inhalation sections of male bellows with a clear pulse-train structure and stable spectral prominences for the analysis of source- and filter-related features. Descriptive statistics for all the acoustic measures are given in Table 1.
Inter-individual differences in male vocal characteristics A discriminant functions analysis (DFA) correctly classified 87.7% of 276 bellows to the 20 males, falling to 79.0% when the more conservative leave-one-out cross validation was applied. Compared to that expected by chance the level of classification was statistically significant for each individual and across all individuals (see Table 2: all P < 0.001 )
In addition, the univariate analysis showed that all the acoustic features measured except
minimum F0 differed significantly between individuals (see Table 1). Furthermore, 81.3% of bellows recorded on the last day for each individual were correctly classified using models trained with calls recorded on the other previous days, confirming that vocal individuality was stable across different days. The examination of the structure matrix shows that the main contributors to individual vocal distinctiveness were filter-related acoustic features, in particular the upper spectral prominences (F4–F6) and
DF (see Table 3). In contrast, source-related features mainly loaded onto discriminant functions 3&4 that together only
explained 16.8% of the variance and hence, were far poorer at classifying male bellows to individuals (see Table 3).
Discrimination of caller identity A general linear model showed that the first look duration of subjects was significantly affected by playback type ( F1,10 = 6,205, P = = 0.008). Pairwise comparisons indicated a significant increase in
first look duration between the last playback of the habituation
Discussion Inter-individual differences in male vocal characteristics
The DFA confirmed that male koala bellows are highly individually distinctive, with 87% of calls correctly assigned to Individual callers (falling to 79% when the more conservative leave-one-out, cross validation approach was used). Indeed, because individual differences in vocal production anatomy directly affect the spectral acoustic structure of the emitted signal [25,35], the presence of identity cues in mammal vocal signals is not surprising. Our results confirm the prominent role of filterrelated features as cues to identity in male koalas. In contrast, source-related features were far poorer at classifying male bellows to individuals, perhaps due to their greater propensity to change according to the caller’s motivational state [26,36]. Other studies on humans and nonhuman mammals have emphasized the importance of filter-related acoustic features as cues to individual identity [2,26,36–38]. In particular, formants are likely to be a reliable source of identity cues in mammals that do not perform dynamic vocal tract modifications during call production (so that the formants are comparatively stable within individuals across calls) and in which the source energy of the call adequately highlights the caller’s distinctive formant pattern (Rendall et al., 1998; Owren and Rendall 2003; Rendall, 2003).
Because the spectral prominences of male koala bellow inhalation
phases are relatively stable (see Figure 1b), and therefore consistent among the calls an individual makes, they are likely to be highly individually distinctive. In addition, observations of male bellow spectrograms and power spectra show a pulse-train structure that should emphasise characteristics of the supra-laryngeal filter (see Figure 1b), increasing their salience to receivers (as discussed by [39,40,41]). Accordingly, the pulse-train structure of male koala bellows may even have evolved to facilitate vocal recognition by highlighting a caller’s distinctive formant pattern. It is interesting to note that the average frequency spacing based on the first six spectral prominences of the inhalation phases of male bellows was 356 Hz. If these spectral peaks represent formants then using the following equation: VTL= c/2 F where c is the approximate speed of sound in the mammalian vocal tract (350 m/s) and DF is the formant frequency spacing, this predicts a
vocal tract length of 49 cm. Post mortem investigations and magnetic resonance imaging scans indicate, however, that male koala supra-laryngeal vocal tract length is much shorter than this, with a resting larynx position that affords a vocal tract length of around 15 cm (Charlton & Fitch et al. Unpublished data). Further anatomical investigations show that the sterno-thyroid muscles are anchored very deep in the thoracic cavity (Charlton & Fitch et al. Unpublished data). While this may indicate that koalas have the ability to retract the larynx to the sternum during vocalizations, this would still only increase vocal tract length to around 20 cm (the distance from the incisors to the sternum: unpublished data) and hence, could not explain our observations. Nevertheless, since the spectral prominences are not harmonically related (i.e., they are not multiple integers), are separated by over 300 Hz, and present in sections of bellows with a stable and fundamental and thus, are likely to represent supra-laryngeal
resonances. Future research employing visual imaging techniques will be needed to further examine the anatomical basis for our findings. As it stands, however, cues related to vocal tract filtering appear to contribute the most to vocal identity in male koala bellows.
Discrimination of caller identity The playback experiments show that koalas can discriminate between the bellow vocalizations of different males. In addition, because the subject’s sex did not affect their propensity to dishabituate or rehabituate (as indicated by the lack of a significant interaction between subject sex and playback type), we suggest that the identity of male koalas is important for both sexes. Whether koalas are able to vocally recognise different males or if they just discriminate between the vocalisations of different callers is less clear. Nevertheless, our demonstration that koalas react to changes in male callers indicates that vocal recognition of males could occur in reproductive contexts, and that the identity of male callers is functionally relevant to male and female koalas during the breeding season. Previous studies investigating vocal recognition in mammals typically focussed on mother-offspring recognition [11,12], and calls produced in the contexts of group cohesion [6,8,42] and alarm calling [9,10]. Very few studies to date have considered the role of vocal recognition in sexual contexts (but see [31,43]) and none in a marsupial species. Male koalas often bellow after agonistic interactions and in response to other bellows [20,23]. Individually distinctive bellows could, therefore, allow males to make judgements on whether or not to escalate competitive interactions based on their previous experience with a given general location for several years and stable dominance hierarchies are reported to exist [20]. Thus, adult male koalas could learn to identify other males in their vicinity and individual vocal characteristics may enable the establishment of specific dominance relationships (as suggested in other seasonal breeders: [19,44,45]).
Female koalas could also become familiarised to the bellows of high quality/dominant males that can outcompete rivals and prefer these individuals in mate choice contexts [18,19,43]. Indeed, vocal recognition in these contexts is especially likely to be important in this arboreal, relatively cryptic species in which other sensory modalities may be less efficient for signalling identity. The particular features that koalas attend to when discriminating between callers is not known. However, our acoustic analysis indicated that F4–F6 were the most individually distinctive acoustic features of male bellows and consequently, these acoustic features could be important for vocal recognition. Furthermore, while the overall pattern of filter-related acoustic features is likely to be distorted by attenuation effects that will not be constant across the frequency domain (as found in elephants: [42]) koalas may even be able to discriminate between male callers based on F4–F6 alone. Future work should re-record male bellows in eucalyptus forests to assess the degradation of specific acoustic features and determine the distances over which information on caller identity could realistically be broadcast. In addition, resynthesis techniques could be used to standardise the values of F4–F6 across habituation–discrimination sequences, in order to investigate the importance of these filter-related acoustic features for vocal recognition in this species.
To conclude, male koala bellows are highly individually distinctive and filter-related features contribute the most to vocal identity. In addition, our results show that male and female koalas react to a change in the identity of male callers, indicating that caller identity is functionally relevant to both sexes during the breeding season. The precise function of signalling caller identity in this species remains a topic for future research; however, we suggest that vocal recognition may be important for males and females in the contexts of intra-sexual competition and mate choice, respectively. Furthermore, since male koala bellows are individually distinctive, the acoustic structure of these calls might be used as a bioacoustic tool for assessing local population densities. This type of information is crucial for determining the conservation status of specific populations and is difficult to obtain in koalas, because they are relatively cryptic and typically occur in low abundance [21]. However, given the high rates of male koala vocal activity during the 3–4 month breeding season [22], remote recording sensors could capture enough good quality recordings for bioacoustic techniques to be used to help distinguish between different individuals. Because koala sex ratios are fairly uniform [21] the adult population size could then be estimated by extrapolation, aiding management and conservation efforts in this iconic species.
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