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29 Cards in this Set
- Front
- Back
proximate causes of behaviour |
ontogeny (learning + maturation) and physiological mechanisms |
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ultimate (historic) causes of behaviour |
impact on reproductive success + origins/evolution |
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ultimate cause of prairie voles |
monogamous prairie voles produce more offspring with genes for monogamy than polygynous prairie voles; this is an ultimate cause |
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history of monogamous voles |
polygynous males who dominate other males --> infanticidal males who gain mates by disposing their pups --> proiscuous females who protect their young against infanticide --> mate-guarding males who provent female promiscuity --> parental males who care for their offspring --> monogamous pairs |
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more on proximate causes |
genetic developmental mechanisms; effects of heredity on behaviour; gene-environment; sensory |
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monogamy in prairie voles --> specific gene? |
v1ar gene in ventral pallium huddle more closely with a female partner after mating than males who lack this gene. |
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proximate questions |
what happens during development to result in emergence of song learning and variations//does operation of the brain differ among males who sing and females who do not |
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ultimate questions |
do differences among individual males in song ability determine reproductive success, and are differences in song learning rooted in evolutionary questions? |
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zebra finch |
Hearing is critically important for song learning in the zebra finch, shown by a sonogram of a male's song to his two male offspring. first son's hearing was intact and he was able to copy father's song accurately, whereas second son was deafened early in life and never sang a typical zebra finch song. |
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how do we know if regional differences are genetic or environmental? |
isolated young birds in lab, found that white-crowned sparrows maybe have a critical period of 10-50 days after hatching when their neural systems can acquire information (according to this hypothesis). |
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more about white crowned sparrows! |
caged next to a strawberry finch will learn the song of its social tutor; |
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sonograms of contact calls of galahs + pink cockatoos |
Discovered that social and acoustic elements are needed. |
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experimental design |
compare male song learners and female brains; males have zz chromosomes + females have zw; zz chromosomes --> gonads --> testosterone --> song learning centers. For females, zw --> estrogen --> no song learning BUT, high levels of estrogen injected into females = singing. Males have a higher concentration of brain estrogen than females do. |
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song competition in the starling |
the RA of males exposed to high-quality songs when they are adults increases in size, unlike some other song control nuclei. |
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song learning in the swamp sparrow |
something ? |
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ZENK activation in ingress |
this activation occurs in the ventral caudomedial neostriatum when female hears song; thereafter she preers perch when long version of the song is played. |
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arcopallium |
RA in zebra finches; much bigger in males than females |
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Neural plasticity |
HVC responds to specific part of a song when learning or producing, when adolescent begins matching song to memory template, strong activation of ZENK gene in area x occurs, then ZENK activation decreases as song becomes a closer match to template; song becomes generally fixed when ZENK activation ceases. |
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ultimate causes of song learning |
newest phylogeny (2008) indicates that song learning evolved just twice, in ancestor of songbirds and of parrots (similar), and in hummingbirds |
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the eastern phoebe |
a member of the passeriformes that don't need to hear others sing in order to produce a song on its own. Learning does not figure in the development of song |
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Bird song repel territorial intruders? |
Territories from which resident male white-throated sparrows were experimentally removed attracted fewer intruders when the taped song was broadcast from vacant territory |
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songs match habitats |
great tits from dense forests produce pure whistles of relatively low frequency, whereas males that live in more open places use more and higher sound frequencies in their more complex songs. |
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type matching: |
targent bird responds to type a song with type a song |
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repertior matching: |
target bird does not respond with same type song, but with one in shared repertior |
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mismatch: |
target bird responds with song that is not shared |
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song matching and communication of aggressive intent |
song sparrow males control level of conflict by their selection of songs; when a focal male sings a shared song at a rival, the neighbour has three options: 1. keep contest at the same level, 2. escalate contest 3. de-escalate conflict |
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cassin finches are examples of directing their songs at females |
evidence for this: when paired with a female on day one, he sings only a little bit; but he invests a lot more time in singing when she leaves. |
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environmental effects on singing |
nutritional stress early in life means that song learning and HVC development decline (as seen in experiments in the swamp sparrow). |
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