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Minimum Frequencies (minimum + frequency)
Selected AbstractsIndividual Acoustic Variation in Fallow Deer (Dama dama) Common and Harsh Groans: A Source-Filter Theory PerspectiveETHOLOGY, Issue 3 2007Elisabetta Vannoni Mammals are able to distinguish conspecifics based on vocal cues, and the acoustic structure of mammal vocalizations is directly affected by the anatomy and action of the vocal apparatus. However, most studies investigating individual patterns in acoustic signals do not consider a vocal production-based perspective. In this study, we used the source-filter model of vocal production as a basis for investigating the acoustic variability of fallow deer groans. Using this approach, we quantified the potential of each acoustic component to carry information about individual identity. We also investigated if cues to individual identity carry over among the two groan types we describe: common and harsh groans. Using discriminant function analysis, we found that variables related to the fundamental frequency contour and the minimum frequencies of the highest formants contributed most to the identification of a given common groan. Common groans were individually distinctive with 36.6% (53.6% with stepwise procedure) of groans assigned to the correct individual. This level of discrimination is approximately six times higher than that predicted by chance. In addition, univariate anovas showed significant inter-individual variation in the minimum formant frequencies when common and harsh groans were combined, suggesting that some information about individuality is shared between groan types. Our results suggest that the sound source and the vocal tract resonances act together to determine groan individuality and that enough variation exists to potentially allow individual recognition based on groans. [source] Cross-Sectional and Longitudinal Studies of the Development of Group Differences in Acoustic Features of Coo Calls in Two Groups of Japanese MacaquesETHOLOGY, Issue 1 2006Toshiaki Tanaka Japanese macaques, Macaca fuscata, frequently utter coo calls to maintain vocal contact. Cross-sectional and longitudinal comparisons were conducted on the acoustic features of coo vocalizations of two groups of M. fuscata, Yakushima and Ohirayama groups, to explore the possibility of vocal plasticity. These two groups derive from the same local population but have been separated for more than 34 yr. The Yakushima group is non-provisioned, while the Ohirayama group is provisioned. Initially, coo calls in the two groups were compared cross-sectionally in females ranging from 0 to 18 yr. Mean values of the four variables studied (start, end, maximum, and minimum frequencies) were consistently lower in all age groups of the Ohirayama individuals compared with the Yakushima individuals. Secondly, longitudinal comparisons were conducted on individuals in the 1,4 yr after birth. Mean values of the five frequency variables studied (start, end, maximum, minimum and average frequencies) were again consistently lower in all age groups of Ohirayama compared with Yakushima individuals, although mean values of both groups gradually declined with an increase in age. Inter-group differences were significant at all ages in minimum frequency and at the first, second and third years in start frequency. Longitudinal comparisons of individuals aged 4,11 mo were also conducted. Regarding the four variables that differed between the two groups in the cross-sectional study, the mean values of minimum and start frequency did not differ significantly between the two groups at 4,5 mo, but were significantly lower in Ohirayama individuals aged 7,8 and 9,11 mo. Although provisioning may have had an effect on the weight difference between the groups, and consequently on vocalization frequency, these results suggest that the inter-group differences in coo call features form approximately 6,7 mo after birth as a result of vocal plasticity. [source] Plant regeneration directs changes in grassland composition after extreme drought: a 13-year study in southern SwitzerlandJOURNAL OF ECOLOGY, Issue 4 2004A. STAMPFLI Summary 1The cover of plant species was recorded annually from 1988 to 2000 in nine spatially replicated plots in a species-rich, semi-natural meadow at Negrentino (southern Alps). This period showed large climatic variation and included the centennial maximum and minimum frequency of days with , 10 mm of rain. 2Changes in species composition were compared between three 4-year intervals characterized by increasingly dry weather (1988,91), a preceding extreme drought (1992,95), and increasingly wet weather (1997,2000). Redundancy analysis and anova with repeated spatial replicates were used to find trends in vegetation data across time. 3Recruitment capacity, the potential for fast clonal growth and seasonal expansion rate were determined for abundant taxa and tested in general linear models (GLM) as predictors for rates of change in relative cover of species across the climatically defined 4-year intervals. 4Relative cover of the major growth forms present, graminoids and forbs, changed more in the period following extreme drought than at other times. Recruitment capacity was the only predictor of species' rates of change. 5Following perturbation, re-colonization was the primary driver of vegetation dynamics. The dominant grasses, which lacked high recruitment from seed, therefore decreased in relative abundance. This effect persisted until the end of the study and may represent a lasting response to an extreme climatic event. [source] |