Seasonal and diel plasticity of song type use in individual ovenbirds ( Seiurus aurocapilla)

Ethology ◽  
2020 ◽  
Vol 126 (8) ◽  
pp. 824-838
Author(s):  
Megan J. Thompson ◽  
Kendriah A. Pearse ◽  
Jennifer R. Foote
The Condor ◽  
2006 ◽  
Vol 108 (2) ◽  
pp. 326-335 ◽  
Author(s):  
David M. Logue

Abstract In many duet-singing songbirds, paired birds combine their song types nonrandomly to form duet songs. Several different behavioral mechanisms could generate nonrandom song type associations in duets. I tested female Black-bellied Wrens (Thryothorus fasciatoventris) for one such mechanism: adherence to a set of rules linking female response songs to male stimulus songs. I call this set of rules a “duet code.” Duets of free-living Black-bellied Wrens were recorded in 2001 and 2002. In 2003 I returned to the same territories and played the male song types from the recorded duets. Females answered male song stimuli as if duetting with the playback speaker. Although the known repertoires of females averaged 8.4 song types, each female sang only a single song type in response to each male song type. Random answering could not account for this pattern, supporting the hypothesis that females abide by duet codes. Females that were still paired with their mates from 2001–2002 answered 100% of their mate's songs with the same song types they had used previously, demonstrating that codes are stable over time. In contrast, females that were new to a territory answered an average of only 18% of their mate's song types with the same song type as the previous female, indicating that duet codes are individually distinctive. Duet participation by female Black-bellied Wrens represents a special kind of animal communication, in which discrete vocal signals consistently elicit discrete vocal responses according to an individually distinctive set of rules.


2018 ◽  
Vol 140 ◽  
pp. 161-170 ◽  
Author(s):  
Richard W. Hedley ◽  
David M. Logue ◽  
Lauryn Benedict ◽  
Daniel J. Mennill

2017 ◽  
Vol 284 (1864) ◽  
pp. 20171774 ◽  
Author(s):  
Paweł Ręk ◽  
Robert D. Magrath

Many group-living animals cooperatively signal to defend resources, but what stops deceptive signalling to competitors about coalition strength? Cooperative-signalling species include mated pairs of birds that sing duets to defend their territory. Individuals of these species sometimes sing ‘pseudo-duets’ by mimicking their partner's contribution, but it is unknown if these songs are deceptive, or why duets are normally reliable. We studied pseudo-duets in Australian magpie-larks, Grallina cyanoleuca , and tested whether multimodal signalling constrains deception. Magpie-larks give antiphonal duets coordinated with a visual display, with each sex typically choosing a different song type within the duet. Individuals produced pseudo-duets almost exclusively during nesting when partners were apart, but the two song types were used in sequence rather than antiphonally. Strikingly, birds hid and gave no visual displays, implying deceptive suppression of information. Acoustic playbacks showed that pseudo-duets provoked the same response from residents as true duets, regardless of whether they were sequential or antiphonal, and stronger response than that to true duets consisting of a single song type. By contrast, experiments with robot models showed that songs accompanied by movements of two birds prompted stronger responses than songs accompanied by movements of one bird, irrespective of the number of song types or singers. We conclude that magpie-larks used deceptive pseudo-duets when partners were apart, and suppressed the visual display to maintain the subterfuge. We suggest that the visual component of many species' duets provides the most reliable information about the number of signallers and may have evolved to maintain honesty in duet communication.


2011 ◽  
Vol 89 (11) ◽  
pp. 1027-1040 ◽  
Author(s):  
J. Pitocchelli

Studies of macrogeographic variation in birdsong involve populations incapable of interbreeding because of physical barriers or separation by large distances. Different patterns have emerged from these studies such as (i) little or no variation exists among individuals or populations from the breeding range, (ii) individual variation is greater than among population variation resulting in no geographic structure, (iii) clinal variation, and (iv) macrogeographic variation where all individuals from several populations on the breeding range share a common song type forming a regional dialect or regiolect. I studied macrogeographic variation in song of the Mourning Warbler ( Oporornis philadelphia (A. Wilson, 1810)). The observed pattern was similar to the fourth category of geographic variation with regiolects. A Western regiolect extended from northern Alberta to western Ontario. An Eastern regiolect stretched eastward from western Ontario and Wisconsin to the Gaspé Peninsula and New England, then southward through the Appalachians to West Virginia. Nova Scotia and Newfoundland each had unique regiolects. Finally, I compared these results to other species with regiolects and assessed the ability of some deterministic hypotheses to explain song divergence (e.g., role of morphology, physical barriers, island isolation).


The Auk ◽  
2006 ◽  
Vol 123 (1) ◽  
pp. 82-96
Author(s):  
Brady J. Mattsson ◽  
Gerald J. Niemi

Abstract Microsite, patch, and landscape conditions may interact to influence nest predation. In northern Minnesota, silvicultural and agricultural practices may be involved in recent increases in nest predators and regional declines in several ground-nesting songbirds. To examine this problem, we evaluated 17 hierarchical models of predation on Ovenbird (Seiurus aurocapilla) nests that included microsite variables, distances to edges, and amount of core forest within a 2-km radius surrounding six study plots. During 2000 and 2001, 157 Ovenbird nests were monitored to estimate nest predation rates. A model that included the main effects of litter depth and core forest area and an interaction term between the two best described variation in predation on Ovenbird nests (AICc weight = 0.83). The nest predation rate from this model was 0.51 ± 0.01 (mean ± SE), assuming mean values of litter depth and amount of core forest. Shallow litter was associated with higher nest predation in three plots surrounded by less core habitat (40–60 ha), whereas there was no relationship in three plots surrounded by more core area (100–150 ha). Management that promotes deep leaf litter and the maintenance of large, intact forest tracts will likely benefit Ovenbirds and other forest songbirds. Factores que Influencian la Depredación de Nidos de Seiurus aurocapilla en los Bosques del Norte: Interacciones a través de las Escalas Espaciales


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