Section 4 Flashcards

1
Q

Research 4.3: Environmental Effects on ZEBRAFISH Aggression

A

1) Christoper Marks examined how water conditions during development affect aggressive behaviour in adult zebrafish
2) In the Himalayas, they live in either rich fast-flowing streams or oxygen-poor pools
3) Oxygen depletion can impact development and behaviour
4) Researchers raised closely related zebrafish in water that had either low or high oxygen levels and examined aggressive behaviour in adults when placed in each environment

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2
Q

ZEBRAFISH: Research Question

A

How does environmental variation affect aggression in zebrafish?

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3
Q

ZEBRAFISH: Hypothesis

A

Both developmental environment (DE) and behavioural (test) environment (TE) affect aggression

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4
Q

ZEBRAFISH: Methods

A

a) collected eggs
b) divided eggs into two developmental environments, normoxic or hypoxic
c) tested fish in either normoxic or hypoxic test chambers (16 hour acclimation)
d) measured aggression as time spent biting or nipping a mirror image

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4
Q

ZEBRAFISH: Results

A

Hypoxia-raised fish had higher levels of aggression in the hypoxic test chamber, and normoxia-raised fish had higher levels of aggression in the normoxic test chamber.

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5
Q

ZEBRAFISH: Conclusion

A

Zebrafish display more aggressive behaviour in the environment in which they were raised, indicating an interaction between developmental and behavioural environments

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6
Q

Research 4.3: Social Environment and Gene Expression in Fruit Flies

A

a) Lisa Ellis and Ginger Carney
b) Consider that behavioural interactions between two conspecifics often depend on the sex: male-male is aggressive, male-female involves courtship

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7
Q

FRUIT FLIES & SOCIAL ENVIRONMENT: Research Question

A

Why might differences in the social environment affect behaviour?

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8
Q

FRUIT FLIES & SOCIAL ENVIRONMENT: Methods

A

a) Used microarray analysis to examine gene expression in male fruit flies exposed to different social environments
b) Raised male flies and exposed them to one of two treatment groups or controls
c) One treatment group could court a single female while the other interacted with a rival male, 20 minutes
d) Control males did not interact with any fly

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9
Q

FRUIT FLIES & SOCIAL ENVIRONMENT: Results

A

a) Identified hundreds of genes that were socially responsive
b) 505 responded to male-male interactions and 281 responded to male-female
c) Most were found in both treatments but 240 were responsive to males only, 16 to females only

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10
Q

Songbird Background Context

A

a) All birds produce calls, which are innate
b) Many produce more complex vocalizations (songs) which are used to defend a territory and attract mates
c) In many songbird species, only males sing (in tropical species, both sing)
d) Song learning occurs in several stages, and species are either closed or open-ended learners

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11
Q

BIRDSONG DEVELOPMENT & SOCIAL ENVIRONMENT: Explain the difference between closed-ended learners and open-ended learners

A

Closed-ended: must hear a tutor sing its conspecific song shortly after hatching, a fixed sensitive period exists
Open-ended: can acquire new song elements throughout life
EXAMPLE: Zebra Finches are closed-ended learners

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12
Q

Research 4.3: Social Environment and Gene Expression in Birds

A

a) Brains of songbirds have enlarged and interconnected areas involved in song memory and production
b) Song System - an area of the brain, consisting of a posterior nucleus, which controls sound production, and an anterior nucleus involved in sound learning (Area X)
c) Exposure to conspecific birdsong causes many genes to be expressed in different regions of the song system
d) FOXP2 and ZENK

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13
Q

BIRDSONG DEVELOPMENT & SOCIAL ENVIRONMENT: Research Question

A

What is the role of the FoxP2 gene in birdsong development?

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14
Q

BIRDSONG DEVELOPMENT & SOCIAL ENVIRONMENT: Methods

A

a) FoxP2 undergoes increased gene expression in Area X of a bird’s brain both when young birds learn to sing and when open-ended learning adults change their song, suggesting FoxP2 plays a role in song learning
b) Reduced FoxP2 levels in Area X before young zebra finches began to learn their song
c) Knockdown technique involved using a virus to insert short sections of RNA into the FoxP2 gene at two different locations to reduce expression
d) Subjects were kept in a sound-isolation chamber with an adult male tutor during the critical period of learning
e) Sonograms were used to reveal number of song elements and characteristic features

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15
Q

BIRDSONG DEVELOPMENT & SOCIAL ENVIRONMENT: Results

A

a) In knockdown birds, FoxP2 expression was reduced by approximately 70%, which affected song development
b) Knockdown birds tended to omit specific syllables and failed to copy accurately the duration of some song syllables
c) Concluded that FoxP2 is required for normal song development

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16
Q

Gene-Environment Interactions

A

a) When G x E is present, we observe variation among genotypes in their responses to environmental variation
b) Now, phenotypic variation (VP) is a result of three factors: genotype variation, environmental variation, and variation from their interactions

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17
Q

Research 4.3: Rover and Sitter Foraging Behaviour in Fruit Flies

A

a) Marla Sokolowski’s work on the foraging behaviour of larval fruit flies
b) Fruit fly eggs develop during a series of larval stages, the larvae crawl to food source, eat, and then molt as they increase in size
c) Larvae exhibit two behavioural polymorphisms: rover and sitter
d) Rovers have longer foraging trails than sitters in the presence of food and are more likely to leave a food patch
e) Difference is due to different alleles at the “for” gene
f) 70% have the dominant rover allele “forR” while 30% are homozygous for the sitter allele “forS”
g) Polymorphism is maintained by frequency-dependent selection: rover allele has higher fitness in crowded conditions where they can benefit by traveling farther to find food and vice versa
h) In the absence of food, rovers behave like sitters since there’s no benefit to moving
i) Suggests a G x E interaction since rover behaviour changes strongly with environmental variation but sitters do not

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18
Q

ROVER & SITTER FORAGING IN FRUIT FLIES: Research Question

A

Do different behavioural polymorphisms in fruit flies exhibit gene-environment interactions?

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19
Q

ROVER & SITTER FORAGING IN FRUIT FLIES: Methods

A

a) examined the behaviour of groups of 25 to 30 adult rovers and sitters exposed to varying levels of food availability
b) half placed in holding vials that contained food for 16 to 18 hours before behavioural testing
c) other half were placed in a food-deprived environment
d) they examined the flies’ movement behaviour with a horizontal plexiglas maze
e) they placed the flies in a vial with food and allowed them to feed, before allowing them to leave the patch and move through the maze, empty glass vials were placed at all maze exits
f) recorded the proportion of flies in the collecting vials after three minutes

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20
Q

ROVER & SITTER FORAGING IN FRUIT FLIES: Results

A

a) The behaviour of fed versus food-deprived rovers and sitters were quite different
b) Fed rovers had a much higher food-leaving score than food-deprived rovers
c) However, there was little difference between the behaviour of fed sitters and food-deprived sitters
d) Can see that different environmental conditions have less effect on the behaviour of the sitter genotypes compared to rovers
e) They used mass spectroscopy to determine the compounds stored in the flies’ head
f) Rovers and sitters store energy differently, fed rovers and fed sitters stored the same levels of lipids but without food, sitters stored more lipids and carbohydrates
g) This indicates that G x E interactions affect both behavioural and metabolic traits

21
Q

Research 4.4: Scouting Behaviour in Bees

A

a) The honeybee has had its entire genome sequenced
b) They live in large colonies and adults exhibit marked differences in behaviour
c) 25% acts as food scouts in the colony, searching for new food sources
d) Non-scouts never embark on searches but learn about new locations when scouts perform a dance

22
Q

HONEYBEES SCOUTING: Methods

A

a) Identified food scouts using a large outdoor flight cage
b) All individuals were first trained to obtain food from a single available source, a training feeder with unscented sugar and a yellow floral pattern
c) Every bee that visited the feeder was marked with a spot of paint
d) After 3 days, a second food source with a novel odour and pattern was added a a new location within the same cage
e) All scouts were paint-marked and held until the end of the day to prevent them from recruiting others
f) After three more days, the process of replacing a novel food repeated
g) Scouts were identified as the bees that found at least two or more new food sources

23
Q

HONEYBEES SCOUTING: Results

A

a) 16% of the mRNA transcripts exhibited significant differences between scout and non-scout brains
b) many of the genes were related to neurotransmitter signalling involving catecholamine, and GABA

24
Q

HONEYBEES SCOUTING: Conclusion

A

Gene products in novelty-seeking individuals differ from those of bees that do not search for new food sources

25
Q

Research 4.4: Alternative Mating Tactics in Black-faced Blennies

A

a) Reproducing is an important adaptive behaviour
b) Defending a territory for mating is costly since they spend time chasing away rival intruder males, reducing time for feeding
c) RECALL: Sneaker males try to invade a male’s territory to fertilize female eggs and are generally smaller
d) In the non-reproductive season, all adult males and females have a dull camouflaged body colour
e) However, during reproductive season, males rapidly develop a black head and bright yellow body and defend territories where they attract females to lay eggs
f) This colour change is transitory and only observed during reproductive season but all males are capable of developing territorial colour

26
Q

BLACK-FACED BLENNIES & ALTERNATIVE MATING: Research Question

A

Are the behavioural and morphological differences among territorial and sneaker males correlated with different levels of gene expression?

27
Q

BLACK-FACED BLENNIES & ALTERNATIVE MATING: Methods

A

a) Examined whole-genome gene expression differences between three phenotypes by performing de novo assembly of RNA: territorial males, sneaker males, and females

28
Q

BLACK-FACED BLENNIES & ALTERNATIVE MATING: Results

A

a) Territorial males differentially expressed more genes than sneaker males and females
b) Maintaining territorial morphology may require more genes to be expressed
c) There was a greater difference between the two male phenotypes than male and female, indicating male phenotypic plasticity: the ability to change behaviour and morphology during reproductive season which is more strongly associated with differential gene expression than difference in sexual dimorphism

29
Q

Research 4.5: Heritability of Exploratory Behaviour in Free-Living Great Tits

A

a) Previous work displayed that individuals exhibited differences in exploratory behaviour, indicative of personalities
b) Some actively explore their new environment quickly and others are more shy to explore

30
Q

GREAT TITS & EXPLORATORY BEHAVIOUR: Research Question

A

Is exploratory behaviour in great tits a heritable trait?

31
Q

GREAT TITS & EXPLORATORY BEHAVIOUR: Hypothesis

A

Exploratory behaviour has a genetic component

32
Q

GREAT TIT & EXPLORATORY BEHAVIOUR: Methods

A

a) Placed individuals in an artificial nest with fake wooden trees
b) Recorded number of flights and hops as an index of exploratory behaviour

33
Q

GREAT TITS & EXPLORATORY BEHAVIOUR: Results

A

The parent-offspring regression on exploratory behaviour was positive

34
Q

GREAT TITS & EXPLORATORY BEHAVIOUR: Conclusion

A

Exploratory behaviour has a genetic component and is a heritable trait

35
Q

GREAT TITS & EXPLORATORY BEHAVIOUR: Selection Experiment

A

a) separated adults into two groups: lowest exploratory scores and highest
b) Next generation of these groups were chosen as the initial breeding generation for two selection lines
c) In each line, nine pairs of birds were used for breeding, which repeated for four generations
d) The nine males and females with highest and lowest scores were selected for breeding
e) Found strong changes in exploratory behaviour of the two lines over four generations
f) By fourth generation, average exploratory score for individuals in the fast line was over four times other than that of individuals in the slow line
g) This illustrates that behavioural variation within a single individual is constrained by its gene alleles

36
Q

Research 4.5: Bold and Shy Personalities in Streamside Salamanders

A

a) Live primarily in deep pools of of shallow streams, these pools are separated by shallow areas of faster-flowing water where they deposit eggs
b) Developing larvae face two challenges before they undergo metamorphosis and leave the stream: they must maximize feeding time to shorten their development time before streams and pools dry up AND they must avoid predators like Green Sunfish
c) When predators are present, larvae can seek shelter under rocks but this reduces feeding time

37
Q

STREAMSIDE SALAMANDER PERSONALITIES: Research Question

A

How do salamander larvae respond to predation risk?

38
Q

STREAMSIDE SALAMANDER PERSONALITIES: Hypothesis

A

An individual’s genotype constrains its behaviour by limiting its flexbility

39
Q

STREAMSIDE SALAMANDER PERSONALITIES: Methods

A

a) Collected ten egg masses to obtain four individual siblings from each
b) Placed each larva in an aquarium that contained a refuge (hiding rock)
c) Exposed each larva to two experimental treatments
d) High Predation Risk Treatment: water from an aquarium containing four sunfish was added
e) Low Predation Risk Treatment: tap water was added
f) Recorded behaviour every 30 minutes for ten hours

40
Q

STREAMSIDE SALAMANDER PERSONALITIES: Results

A

a) Larvae in the control treatment spent more time out of the refuge eating than did larvae with predators
b) Found a significant positive correlation in the amount of time each larva spent out of the refuge across treatments: individuals that spent more time in the open in the control also spent more time in the open in the predator treatment

41
Q

STREAMSIDE SALAMANDER PERSONALITIES: Conclusion

A

Genetic differences across individuals explain the consistent relative differences in activity level across treatments, indicating that salamanders do exhibit behavioural personalities

42
Q

STREAMSIDE SALAMANDER PERSONALITIES: More

A

a) An individual that spent much time out of the refuge when no predators were present also spent much time out of the refuge when predators were present, acting bold
b) Few fish were able to optimize and spend a lot of time away when no predators were there but then feast when predators were gone
c) Genetic differences underlie the observed behavioural differences, we see how genotype can limit behavioural plasticity

43
Q

Research 4.5: Animal Personalities Model with Fitness Trade-Offs

A

a) Model with two personality traits: superficial and thorough exploratory behaviour
b) Model organism lives for two years and can reproduce each year
c) High and low quality resources exist in the environment but high quality is hard to find
d) It takes a year to find so those that explore thoroughly will have high quality but only reproduce in year two, but have higher reproductive success when they finally do
e) Through simulations, they found that each exploration strategy can yield equal fitness so personality traits can coexist in a population
f) In real studies, on average, bold individuals tended to have higher reproductive success but also tended to have a shorter lifespan, giving shyer individuals more opportunities to reproduce, which proves the simulation’s point that different personalities can have equal fitness

44
Q

Research 4.5: Environmental Effects on Jumping Spider Personalities

A

a) Do environmental factors affect the development of behavioural types?
b) Examined how a rearing environment affected exploratory behaviour in adult jumping spiders
c) They are active hunters that live in a variety of habitats and need to search for prey

45
Q

JUMPING SPIDER PERSONALITIES: Research Question(s)

A

(1) Do adults exhibit consistent differences in their level of exploratory behaviour (personality)
(2) Does the complexity of a rearing environment affect adult personality?

46
Q

JUMPING SPIDER PERSONALITIES: Hypothesis

A

Development in an enriched physical or social environment would result in greater adult exploratory behaviour

47
Q

JUMPING SPIDER PERSONALITIES: Methods

A

a) Females were captured and mated in the lab to produce 14 maternal lines
b) Offspring were divided into three rearing environments: deprived, physically enriched, or socially enriched
c) Deprived - individuals were reared (raised) alone with no visual contact with species mates
d) Socially Enriched - physically deprived but together with 5-15 siblings
e) Physically Enriched - socially deprived but environment had bark, dry leaves, moss, small plastic items
f) Placed individuals in a small open field, after 30 minutes of acclimatization, spider could leave and explore the arena for 60 mins

48
Q

JUMPING SPIDER PERSONALITIES: Results

A

a) All behaviours measured were repeatable over time, so jumping spiders exhibited different personalities
b) Individuals reared in the deprived environment exhibited the most shyness
c) Physically enriched individuals scored highest in terms of percentage of arena visited

49
Q

JUMPING SPIDER PERSONALITIES: Conclusion

A

Early experiences can influence the development of different behavioural types with respect to exploratory behaviour in adults