Chapter 10 Opener There are both immediate physiological and long-term evolutionary causes for why this male blue-cheeked bee-eater produces vocalizations when communicating with other bee-eaters
Figure 10.1 Evolution by natural selection shapes the mechanisms of behavior, as illustrated by the prairie vole’s mating behavior
Table 10.1 Levels of analysis in the study of animal behavior
Figure 10.2 Recruitment patterns in the honey bee
Figure 10.2 Recruitment patterns in the honey bee (Part 1)
Figure 10.2 Recruitment patterns in the honey bee (Part 2)
Figure 10.2 Recruitment patterns in the honey bee (Part 3)
Figure 10.3 Prairie voles are monogamous
Figure 10.4 The evolutionary relationships of the prairie vole and six of its relatives
Figure 10.5 The brain of the prairie vole, like that of all mammals, is a complex, evolved mechanism with special features whose operation helps explain vole behavior
Figure 10.5 The brain of the prairie vole, like that of all mammals, is a complex, evolved mechanism with special features whose operation helps explain vole behavior (Part 1)
Figure 10.5 The brain of the prairie vole, like that of all mammals, is a complex, evolved mechanism with special features whose operation helps explain vole behavior (Part 2)
Figure 10.6 A gene that affects male pairing behavior in the prairie vole
Figure 10.7 Song dialects in whitecrowned sparrows
Figure 10.8 Hearing and song learning
Figure 10.8 Hearing and song learning (Part 1)
Figure 10.8 Hearing and song learning (Part 2)
Figure 10.9 Song learning hypothesis based on laboratory experiments with white-crowned sparrows
Figure 10.10 Social experience influences song development
Figure 10.11 Social effects on song learning
Figure 10.12 Sonograms of contact calls of two parrots
Figure 10.12 Sonograms of contact calls of two parrots (Part 1)
Figure 10.12 Sonograms of contact calls of two parrots (Part 2)
Figure 10.12 Sonograms of contact calls of two parrots (Part 3)
Figure 10.13 The song preferences of female starlings
Figure 10.13 The song preferences of female starlings (Part 1)
Figure 10.13 The song preferences of female starlings (Part 2)
Figure 10.14 The song system of a typical songbird
Figure 10.15 Difference in the size of one nucleus of the song system
Figure 10.16 Song competition in the starling
Figure 10.16 Song competition in the starling (Part 1)
Figure 10.16 Song competition in the starling (Part 2)
Figure 10.17 Single cells and song learning in the swamp sparrow
Figure 10.17 Single cells and song learning in the swamp sparrow (Part 1)
Figure 10.17 Single cells and song learning in the swamp sparrow (Part 2)
Figure 10.18 Two phylogenies of song learning in birds
Figure 10.18 Two phylogenies of song learning in birds (Part 1)
Figure 10.18 Two phylogenies of song learning in birds (Part 2)
Figure 10.19 The song control systems of parrots, hummingbirds, and oscine songbirds
Figure 10.20 Songs match habitats
Figure 10.20 Songs match habitats (Part 1)
Figure 10.20 Songs match habitats (Part 2)
Figure 10.21 The dialects of whitecrowned sparrows in three parts of San Francisco
Figure 10.21 The dialects of whitecrowned sparrows in three parts of San Francisco (Part 1)
Figure 10.21 The dialects of whitecrowned sparrows in three parts of San Francisco (Part 2)
Figure 10.21 The dialects of whitecrowned sparrows in three parts of San Francisco (Part 3)
Figure 10.22 Two white-crowned sparrow songs from different dialect populations
Figure 10.23 Dialect selection by male white-crowned sparrows
Figure 10.24 Song type matching in the song sparrow
Figure 10.24 Song type matching in the song sparrow (Part 1)
Figure 10.24 Song type matching in the song sparrow (Part 2)
Figure 10.25 Song matching and communication of aggressive intent in the song sparrow
Figure 10.26 Male Cassin’s finches sing to attract females
Figure 10.26 Male Cassin’s finches sing to attract females (Part 1)
Figure 10.26 Male Cassin’s finches sing to attract females (Part 2)
Figure 10.27 Nutritional stress early in life has large effects on song learning by male swamp sparrows
Figure 10.27 Nutritional stress early in life has large effects on song learning by male swamp sparrows (Part 1)
Figure 10.27 Nutritional stress early in life has large effects on song learning by male swamp sparrows (Part 2)
Figure 10.28 The mean number of precopulatory displays in response to differences in song quality
Figure 10.28 The mean number of precopulatory displays in response to differences in song quality (Part 1)
Figure 10.28 The mean number of precopulatory displays in response to differences in song quality (Part 2)