2015
DOI: 10.1007/s10336-015-1238-x
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Composition and sequential organization of song repertoires in Cassin’s Vireo (Vireo cassinii)

Abstract: The rules governing bird song sequences vary considerably across the avian phylogeny, and modifications to these rules represent one of the many ways in which bird song varies interspecifically. Cassin's Vireo (Vireo cassinii) is one species that shows a highly structured syntax, with clearly non-random patterns of sequential organization in their songs. Here I present a description of Cassin's Vireo song sequences from the Sierra Nevada Mountains in California and employ network analysis to quantify transitio… Show more

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Cited by 36 publications
(38 citation statements)
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“…As the N-gram increased, the L 1 -distances for the first-order model diverged from the values for the training set (one-tailed paired t-tests vs training set, p = 0.28 at N = 2, p<0.001 at N = 3 to N = 7), while the values for the second-order model remained similar to those of the training set until N = 6, only showing a significant difference at N = 7 ( Fig 2 ; one-tailed paired t-tests vs training set, p = 0.27 at N = 2, p = 0.23 at N = 3, p = 0.54 at N = 4, p = 0.20 at N = 5, p = 0.081 at N = 6, p = 0.003 at N = 7). The first- and second-order models both produced a similar recurrence interval distribution to that described by Hedley [ 25 ], biased towards low recurrence intervals. Unlike the distributions derived from the zero-order model, these distributions did not differ significantly from the distributions observed in the training sets (one-tailed paired t-tests vs training set: zero-order, p<0.001; first-order p = 0.66; second-order p = 0.99), suggesting that even models that condition transition probabilities on a short preceding sequence can recover apparent longer-term structure in song sequences ( Fig 2 ).…”
Section: Resultssupporting
confidence: 56%
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“…As the N-gram increased, the L 1 -distances for the first-order model diverged from the values for the training set (one-tailed paired t-tests vs training set, p = 0.28 at N = 2, p<0.001 at N = 3 to N = 7), while the values for the second-order model remained similar to those of the training set until N = 6, only showing a significant difference at N = 7 ( Fig 2 ; one-tailed paired t-tests vs training set, p = 0.27 at N = 2, p = 0.23 at N = 3, p = 0.54 at N = 4, p = 0.20 at N = 5, p = 0.081 at N = 6, p = 0.003 at N = 7). The first- and second-order models both produced a similar recurrence interval distribution to that described by Hedley [ 25 ], biased towards low recurrence intervals. Unlike the distributions derived from the zero-order model, these distributions did not differ significantly from the distributions observed in the training sets (one-tailed paired t-tests vs training set: zero-order, p<0.001; first-order p = 0.66; second-order p = 0.99), suggesting that even models that condition transition probabilities on a short preceding sequence can recover apparent longer-term structure in song sequences ( Fig 2 ).…”
Section: Resultssupporting
confidence: 56%
“…Accordingly, each recording was analyzed as a single sequence, regardless of the durations of silence contained therein. A more detailed description of this species’ singing behavior can be found in Hedley [ 25 ].…”
Section: Resultsmentioning
confidence: 99%
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“…For example, Cassin's Vireos (Vireo cassinii; CAVI) have songs made up of phrases, short bursts of notes, <0.7 s in duration, separated by 1 s of silence or more. Each bird will typically have 40-60 phrase types 6 that can be reliably distinguished manually by an observer; doing so automatically is challenging due to within-class variability, limited training data, and noisy environments. This problem shares many features with speech processing in human, while presenting new challenges of its own.…”
Section: Introductionmentioning
confidence: 99%