|
The Acoustic Adaptation Hypothesis does not support the occurrence of common songs in a neotropical urban bird species |
Luis Cueva, Raúl Bartolo & Luis Sandoval |
2024 |
6 |
510-526 |
|
Community algorithms reveal song type themes in Adelaide’s warbler song type sequence networks |
H. R. Petkau, O. J. Medina Rodriguez, P. C. Mower, S. W. Krause, L. R. Mitchell, T. R. Bonnell & D. M. Logue |
2025 |
1 |
60-65 |
|
Singing behaviour of the Western Bonelli’s warbler correlates with social context and environmental factors |
Sandro Carlotti & Gilberto Pasinelli |
2025 |
5 |
509-529 |
|
Identification of nocturnal flight calls of Bicknell’s thrush (Catharus bicknelli) and gray-cheeked thrush (Catharus minimus) |
E. Brisson-Curadeau, Y. Aubry, A. Desrochers, B.M. Van Doren & B. Drolet |
2025 |
5 |
672-690 |
|
A novel song performance constraint on buzzes produced through pulsatile expiration differs from constraints on trills in a songbird (Setophaga cerulea) |
Julian B. Grudens & Kamal Islam |
2025 |
6 |
753-774 |
|
Factors affecting acoustic propagation of birdsong: variation among song types and the effects of habitat on Bachman’s sparrow (Peucaea aestivalis) song |
Hans R. Gonzembach, Heather Wolverton & Rindy C. Anderson |
2026 |
3 |
277-296 |
|
Responses of southern house wrens to rhythmicity of alarm calling sequences |
Gustavo J. Fernández & Mariana E. Carro |
2026 |
3 |
297-317 |
|
The differential effects of low, intermediate, and high amplitudes of anthropogenic noise on the behaviour of an urban-living bird |
Grace Blackburn & Amanda R. Ridley |
2026 |
4 |
417-428 |
