Age-related variation in song repertoire size and repertoire sharing of yellow warblers (Dendroica petechia)

1986 ◽  
Vol 64 (9) ◽  
pp. 1926-1929 ◽  
Author(s):  
Susan E. Cosens ◽  
Spencer G. Sealy
Keyword(s):  
Reproductive Success ◽  
Dendroica Petechia ◽  
Repertoire Size ◽  
Song Repertoire ◽  
Fledging Success ◽  
Related Variation ◽  
Age Related ◽  
Yellow Warblers ◽  
Clutch Initiation

Songs of male yellow warblers (Dendroica petechia), ranging from 1 to 6 years of age, were recorded in the spring and summer of 1984. Recorded repertoire size and number of songs shared with neighbours varied positively with age in the spring but not in summer. Neither clutch initiation date nor fledging success varied with age or number of songs shared but both measures of reproductive success varied with size of recorded song repertoire.

scholarly journals Trill consistency is an age-related assessment signal in banded wrens

2009 ◽  
Vol 276 (1665) ◽  
pp. 2315-2321 ◽  
Author(s):  
Selvino R. de Kort ◽  
Erin R.B. Eldermire ◽  
Sandra Valderrama ◽  
Carlos A. Botero ◽  
Sandra L. Vehrencamp
Keyword(s):  
Sexual Selection ◽  
Competitive Advantage ◽  
Phenotypic Trait ◽  
First Year ◽  
Repertoire Size ◽  
Song Repertoire ◽  
Age Related ◽  
Related Trait ◽  
Structural Aspects ◽  
Older Males

Older males tend to have a competitive advantage over younger males in sexual selection. Therefore, it is expected that signals used in sexual selection change with age. Although song repertoire size in songbirds is often mentioned as an age-related trait, many species, including the banded wren ( Thryothorus pleurostictus ), do not increase their repertoires after the first year. Here, we show that banded wrens reproduce the trill notes in their songs with less variability between them (i.e. more consistently) when they grow older. In a playback experiment, we also show that banded wrens discriminate between younger and older birds based on structural aspects of their song. In a second experiment, banded wrens also respond differentially to natural songs versus songs with artificially enhanced consistency. We argue that consistency in trill note reproduction may be achieved through practice. Sexual selection in the form of male–male competition may therefore operate on a phenotypic trait, the expression of which is enhanced by practice.

Male quality and song repertoires in western meadowlarks (Sturnella neglecta)

1993 ◽  
Vol 71 (5) ◽  
pp. 1059-1061 ◽  
Author(s):  
Andrew G. Horn ◽  
Thomas E. Dickinson ◽  
J. Bruce Falls
Keyword(s):  
Reproductive Success ◽  
Wing Length ◽  
Territory Size ◽  
Male Quality ◽  
Repertoire Size ◽  
Song Repertoire ◽  
Signalling System ◽  
The Relationship ◽  
Sturnella Neglecta ◽  
Song Repertoires

The relationship between song repertoire size and measures of male quality and reproductive success was examined in a Manitoba population of western meadowlarks (Sturnella neglecta). Repertoire size correlated positively with the singer's wing length but not with mass or territory size. Males with larger repertoires tended to pair earlier and males with higher pairing success had larger repertoires. Repertoire size correlated positively with fledging success independently of pairing success. As suggested for other species, repertoire size might serve as a signal to females of male quality. We suggest mechanisms by which this signalling system is maintained.

Egg-size variation in Yellow Warblers: apportionment of parental investment and the brood-survival hypothesis

1993 ◽  
Vol 71 (5) ◽  
pp. 1008-1011 ◽  
Author(s):  
Percy N. Hébert ◽  
Spencer G. Sealy
Keyword(s):  
Egg Size ◽  
Survival Rates ◽  
Size Variation ◽  
Relative Mass ◽  
Egg Mass ◽  
Passerine Birds ◽  
Dendroica Petechia ◽  
Brood Survival ◽  
Yellow Warblers ◽  
Clutch Initiation

It has been hypothesized that in passerine birds the larger size of last-laid eggs is part of a brood-survival strategy. We examined the usefulness of the brood-survival hypothesis in explaining intraclutch variation in egg mass of Yellow Warblers (Dendroica petechia). In 4- and 5-egg clutches, egg mass increased significantly with laying order. Although last-hatched nestlings in broods of 4 had higher survival rates than their counterparts in broods of 5, there were no differences in the absolute or relative mass of last-laid eggs in clutches of 4 and 5 eggs. In addition, the mass of last-laid eggs that hatched but did not produce a fledgling was not significantly different from that of last-laid eggs that did produce a fledgling. Finally, the relative mass of last-laid eggs was also not correlated with hatch spread or with date of clutch initiation. The results of this study do not support the brood-survival hypothesis.

Factors Influencing Age-Related Reproductive Success in the Willow Ptarmigan

The Auk ◽  
1984 ◽  
Vol 101 (4) ◽  
pp. 848-854 ◽  
Author(s):  
Susan J. Hannon ◽  
James N. M. Smith
Keyword(s):  
Reproductive Success ◽  
Clutch Size ◽  
Hatching Success ◽  
Territory Size ◽  
Willow Ptarmigan ◽  
Factors Influencing ◽  
Age Related ◽  
Population Turnover ◽  
Clutch Initiation ◽  
Foraging Skills

Abstract In many species, adult birds lay earlier and have higher reproductive success than do yearlings. We found no difference, however, between adult and yearling female Willow Ptarmigan (Lagopus lagopus alexandrae) in date of clutch initiation, clutch size, hatching success, number of fledged young, or territory size. Adult females defended their broods more vigorously, and more were observed with broods, a situation suggesting that more yearlings lost their eggs or young and did not renest. Pairs composed of two adults produced more fledged young than did pairs composed of two yearlings, but clutch size and date of clutch initiation were similar in the two groups. We suggest that the following factors may allow yearlings to reproduce almost as successfully as adults: (1) a reduction in competition with adults for territories because of high population turnover, (2) the presence of extensive male parental care and precocial young, and (3) a dependence on a food source that is readily available and can be obtained without specialized foraging skills.

scholarly journals Song Sharing by Yellow Warblers Differs Between two Modes of Singing: Implications for Song Function

The Condor ◽  
2002 ◽  
Vol 104 (1) ◽  
pp. 146-155 ◽  
Author(s):  
Martin D. Beebee
Keyword(s):  
Spatial Relationship ◽  
Indirect Evidence ◽  
Song Type ◽  
Type I ◽  
Type Ii ◽  
Dendroica Petechia ◽  
Song Repertoire ◽  
Song Sharing ◽  
Yellow Warblers ◽  
Song Types

Abstract I investigated the pattern of song sharing for the two singing modes (Type I and Type II) of Yellow Warblers (Dendroica petechia). There is indirect evidence that males use Type I singing to attract females, and Type II singing to interact with other males, but how males use these singing modes for these functions is unknown. One way in which males might use Type II singing to interact with neighboring males is through the use of “shared songs:” males might preferentially sing songs they share with neighboring males to engage in song type matching or repertoire matching. I tested the prediction that Yellow Warblers should share more of their Type II songs with neighbors compared to non-neighbors, but that there should be no such relationship for Type I songs. I found that males in a Pennsylvania population shared significantly more of their Type II song repertoire with neighbors than with non-neighbors, and that sharing between males declined with distance between their territories. There was no spatial relationship for sharing Type I song types. These results are consistent with the hypothesis that Yellow Warblers use Type II singing to interact with other males using strategies such as song type and repertoire matching. Dendroica petechia Comparte sus Cantos de Dos Modos Diferentes: Implicancias para la Función del Canto Resumen. Investigué el modo en que Dendroica petechia comparte sus cantos en relación a dos maneras de cantar (Tipo I y Tipo II). Existe evidencia indirecta que los machos usan cantos de Tipo I para atraer a las hembras y cantos de Tipo II para interactuar con otros machos, pero se desconoce cómo los machos usan estos cantos para estas funciones. Una manera en la que los machos podrían usar cantos de Tipo II para interactuar con machos vecinos es a través del uso de “canciones compartidas:” los machos podrían preferentemente cantar canciones que comparten con machos vecinos para establecer el uso de un tipo de canción o repertorio semejante. Puse a prueba la predicción que D. petechia debería compartir una mayor parte de sus canciones de Tipo II con machos vecinos que con no-vecinos, pero que no debería existir esta relación para canciones de Tipo I. Encontré que los machos de una población de Pensilvania comparten una parte significativamente mayor de su repertorio de canciones de Tipo II con vecinos que con no-vecinos, y que el grado en que los machos comparten canciones disminuye con la distancia entre sus territorios. No hubo una relación espacial en los tipos de canciones compartidas de Tipo I. Estos resultados son consistentes con la hipótesis que D. petechia usa canciones de Tipo II como estrategia para interactuar con otros machos empleando tipo de canciones o repertorios semejantes.

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