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Chapter 11 Opener Both genes and environment contribute to the development of foraging behavior in the honey bee
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Figure 11.1 Development of worker behavior in honey bees
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Figure 11.1 Development of worker behavior in honey bees (Part 1)
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Figure 11.1 Development of worker behavior in honey bees (Part 2)
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Figure 11.2 Gene activity varies in the brains of nurse bees and foragers.
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Figure 11.3 Social environment and task specialization by worker honey bees
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Figure Levels of the messenger RNA produced when the for gene is expressed in the brains of nurses and of foragers in three typical honey bee colonies
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Figure 11.5 Imprinting in greylag geese
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Figure 11.6 Cross-fostering has different imprinting effects in two related songbirds
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Figure 11.6 Cross-fostering has different imprinting effects in two related songbirds (Part 1)
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Figure 11.6 Cross-fostering has different imprinting effects in two related songbirds (Part 2)
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Figure 11.7 Spatial learning by chickadees
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Figure 11.7 Spatial learning by chickadees (Part 1)
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Figure 11.7 Spatial learning by chickadees (Part 2)
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Figure A Clark’s nutcracker holding a seed in its bill that the bird is about to cache underground
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Figure 11.9 Kin discrimination in Belding’s ground squirrels
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Figure 11.9 Kin discrimination in Belding’s ground squirrels (Part 1)
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Figure 11.9 Kin discrimination in Belding’s ground squirrels (Part 2)
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Figure 11.10 Belding’s ground squirrels learn their own odor
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Figure 11.11 Migratory routes taken by blackcap warblers in the fall
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Figure 11.11 Migratory routes taken by blackcap warblers in the fall (Part 1)
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Figure 11.11 Migratory routes taken by blackcap warblers in the fall (Part 2)
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Figure Differences in the migratory behavior of two closely related birds, the black redstart and the common redstart
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Figure A coastal Californian garter snake about to consume a banana slug, a favorite food of snakes in this region
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Figure 11.14 Response of newborn, naive garter snakes to slug cubes
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Figure A tongue-flicking newborn garter snake senses odors from a cotton swab that has been dipped in slug extract
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Figure 11.16 Genetic differences cause behavioral differences in fruit fly larvae
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Figure 11.17 A single genetic difference has a large effect on maternal behavior
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Figure 11.18 Social amnesia is related to the loss of a single gene
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Figure 11.18 Social amnesia is related to the loss of a single gene (Part 1)
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Figure 11.18 Social amnesia is related to the loss of a single gene (Part 2)
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Figure 11.19 Surrogate mothers used in social deprivation experiments
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Figure Socially isolated rhesus infants that are permitted to interact with one another for short periods each day at first cling to each other during the contact period
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Figure 11.21 Developmental homeostasis in humans
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Figure 11.22 Developmental switch mechanisms can produce polyphenisms within the same species
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Figure 11.23 Tiger salamanders occur in two forms
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Figure Activity of the gene that codes for gonadotropin-releasing hormone in the cichlid fish Astatotilapia burtoni
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Figure Subordinate males of the fish Astatotilapia burtoni react very quickly to the absence of a dominant rival
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Figure Subordinate males of the fish Astatotilapia burtoni react very quickly to the absence of a dominant rival (Part 1)
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Figure Subordinate males of the fish Astatotilapia burtoni react very quickly to the absence of a dominant rival (Part 2)
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Figure 11.26 Developmental flexibility in redback spiders
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Figure 11.26 Developmental flexibility in redback spiders (Part 1)
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Figure 11.26 Developmental flexibility in redback spiders (Part 2)
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Figure 11.26 Developmental flexibility in redback spiders (Part 3)
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Figure 11.26 Developmental flexibility in redback spiders (Part 4)
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Figure 11.27 Male thynnine wasps can learn to avoid being deceived by an orchid
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Figure 11.27 Male thynnine wasps can learn to avoid being deceived by an orchid (Part 1)
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Figure 11.27 Male thynnine wasps can learn to avoid being deceived by an orchid (Part 2)
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Figure 11.28 Spatial learning abilities differ among members of the crow family
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Figure Male pinyon jays make fewer errors than females do when retrieving seeds from caches they have made, especially after intervals of 2 to 4 months
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Figure Male pinyon jays make fewer errors than females do when retrieving seeds from caches they have made, especially after intervals of 2 to 4 months (Part 1)
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Figure Male pinyon jays make fewer errors than females do when retrieving seeds from caches they have made, especially after intervals of 2 to 4 months (Part 2)
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Figure 11.30 Sex differences in spatial learning ability are linked to home range size
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Figure 11.31 A virtual maze used for computer-based studies of navigational skills
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Figure 11.32 Sex differences in the hippocampus
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Figure 11.33 Operant conditioning exhibited by a rat in a Skinner box
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Figure 11.34 Biases in taste aversion learning
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Figure 11.35 Vampire bats could not form learned taste aversions
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Figure 11.35 Vampire bats could not form learned taste aversions (Part 1)
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Figure 11.35 Vampire bats could not form learned taste aversions (Part 2)
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