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Chapter 3

Development of Behavior

 Development is an interactive process in

which the genes are turned on and off

both in response to environmental change

and simultaneously creating change.



 This demonstrated by changes in behavior

shown by honeybees over the course of

their lives.

Development of Behavior

 Honeybees when they emerge as adults

first work at cleaning cells then as they

age they shift to other tasks.



 Eventuallyat about age 3 weeks they

begin foraging outside the hive.

Development of Behavior

 Asthe bee goes through these changes in

behavior it appears that predictable

changes in the genes being actively

expressed occur.



 Microarraytechnology makes it possible to

scan for activity levels of many genes by

detecting mRNA made when genes are

turned on.

Development of Behavior

 Comparisons of arrays of nurse and

forager bees shows substantial differences

in genes turned on at each stage.

(YN= young nurses, OF = older foragers)

Development of Behavior

 Transition to worker role appears to be strongly

influenced by level of a hormone called juvenile

hormone, which is produced by a gene.



 The juvenile hormone gene turns on apparently

in response to activity of other genes during 1st

three weeks of adulthood , but can also be

turned on in response to conditions in the hive.

Development of Behavior

 If colonies are artificially made up of only young

workers some become foragers much sooner

and others remain as nurse bees much longer.



 It may be social encounters that stimulate these

changes.



 Lack of encounters with older foragers appears

to hasten nurse bees transition to forager role.

Development of Behavior

 Adding numbers of older bees to hives

that contain only young bees reduces the

number of young bees that become

foragers.



 In contrast, adding more young bees does

not slow rate at which young bees become

foragers.

Development of Behavior

 Inhibitingagent believed to be a chemical

called ethyl oleate that foragers

manufacture and store in their crop.



 When foragers transfer food to nurse bees

they transfer the chemical, which slows

the nurses transition to foragers.

Development of Behavior

 Inhoneybees, therefore, sequence of

behavioral changes is determined by

continuous interactions between genes

and both chemical and social

environments.

Nature vs Nurture Debate

 Nature: genetic contribution to behavior.



environmental contribution to

 Nurture:

molding behavior.



 There is a false dichotomy in popular

discussions in which traits are considered

to be genetically or environmentally

determined.

Nature vs Nurture Debate

 Inreality, all traits are the product of

gene-environment interactions.



 As we saw in the process of song learning

there is considerable gene-environment

interaction.

Nature vs Nurture Debate

 Environmentalor genetic differences

among individuals can lead to differences

in development and finally differences in

behavior.

What causes individuals to develop

differently?

 Environmental differences and behavioral

differences.



 Many behavioral differences result from

differences in experience.



 For example, marsh tits fed whole sunflower

seeds, which they can hide and later retrieve,

develop a larger hippocampus in their brain than

birds fed only powdered sunflower seeds.

Practice of storing and retrieving seeds alters

brain development.

Learning of nestmates in Polistes

wasps

 Polistes wasps learn to identify the smell

of their natal nest and tolerate individuals

that smell like the nest (whether or not

they are relatives).



with a different smell are

 Individuals

attacked. Differences in how wasps

behave towards each other thus are based

on the smells they learned when young.

 Similardiscrimination between individuals

reared together versus apart has been

shown in Belding’s Ground Squirrels.



 Non-relativesreared together act nicely

towards each other. However, relatives

reared apart also act nicely towards each

other.

 Ground squirrels apparently learn what they

themselves smell like and use this information to

evaluate their relatedness to other individuals.



 Trials in which squirrels provided with cubes

smeared with dorsal gland secretions of other

individuals respond more strongly to those of

non-relatives and discriminate between different

degrees of relatedness.

Genetic differences and

behavioral differences



 Breedingexperiments can show whether

behavioral differences between

populations have a genetic basis.

Funnel Web Spiders

 Spiders in different habitats differ in their

speed of reaction to food being caught in

their webs.

 Streamside spiders react slowly.

 Desert grassland spiders react quickly.

 Is difference largely environmental or

genetic?

Funnel Web Spiders

 Spiders bred in lab.

 Offspring of both populations kept equally

well fed. Then offered food.

 Desert spider reaction time: 3s.

 Streamside spider reaction time: 60s.

 Most of the difference in behavior

apparently due to genetic differences

between populations.

Migratory behavior of European Blackcaps

Migratory behavior of European

Blackcaps

 Blackcapsare small European warblers,

most of which migrate to Africa to winter.

However, some spend the winter in

Britain.



 What causes this difference in behavior?

Migratory behavior of European

Blackcaps

 Peter Berthold caught wintering blackcaps

in Britain.



 Hethen bred these birds in central

Germany in outdoor cages.

Migratory behavior of European

Blackcaps

 In fall Berthold looked at migratory

direction selected by birds.



 Used an Emlen funnel to record

orientation.

Emlen Funnel

Blackcaps oriented in a westerly direction.









Conclusion? British birds from where?

Migratory behavior of European

Blackcaps

 Basedon orientation birds not from

Scandinavia or northern Britain.



 Birdsprobably from due east of Britain

Belgium or Germany.

Migratory behavior of European

Blackcaps

 Couldenvironmental influences be

responsible?



just being in Germany causes

 Perhaps,

westward orientation.

Migratory behavior of European

Blackcaps

 Tocheck birds from SW Germany were

bred in captivity.



 Migratory orientation was checked.

SW German birds oriented southwest.

Migratory behavior of European

Blackcaps

 Differences in orientation between

populations largely determined by genetic

differences.



 Southwest German birds migrate SW

traveling west of the Mediterranean via

Spain.

Migratory behavior of European

Blackcaps

 AndreasHelbig has shown that Blackcaps

from Austria orient southeast.



 Theytravel east of the Mediterranean via

Turkey and Israel.

Migratory behavior of European

Blackcaps

 Helbig crossed birds from Austria with

birds from southwest Germany.



 What direction did they orient?

Mean orientation of offspring south.





Inner ring

Adults.



Outer ring

Offspring.

Migratory behavior of European

Blackcaps

 Due south is a poor choice. Requires bird

to cross the Alps and the make a long sea

crossing over the Mediterranean.

Single gene effects on

development

 In theory a single gene difference could be

responsible for difference in orientation on

different Blackcap populations.



 Note a single gene does not encode

migratory choices, but a change in a single

gene can result in many gene-environment

effects and ultimately produce a large

behavioral difference.

Two strains of Drosophila differ in

larval foraging behavior.



Rovers move a lot when feeding.

Sitters move very little.



Rover









Sitter

Rover/sitter behavior in

Drosophila

 When the two strains were crossed in the

F1 generation all of the larvae were

rovers.



A cross of members of the F1 generation

produced a 3:1 ratio of rovers to sitters.

Rover/sitter behavior in

Drosophila

 One gene appears to be responsible for

difference between phenotypes.



 The rover allele is dominant and the sitter

allele is recessive. Gene that affects

rover/sitter behavior affects the olfactory

system and may affect fly’s ability to sense

its environment.

Rover/sitter behavior in

Drosophila

 Manyother single gene effects in

Drosophila.



Stuck: males don’t dismount after

 E.g.

normal 20 minutes of copulation.



interruptus: male copulates for only

 Coitus

10 minutes.

Single gene examples from lab

mice

 Micehomozygous for allele for

defective form of  calmodulin kinase

have poor learning ability.

Single gene examples from lab

mice

 Mouse placed in water-filled container.

 Submerged platform available for rest.

 Normal and mutant mice tested with

platform in random locations and original

testing position.

 Time to find platform measured.

When platform kept in same location as in training trials

wild-type mice found platform much faster than mutant mice,

but not if position of platform was randomized.

fosB gene

 In normal mice sniffing and touching pups

causes changes in female’s brain that

prompt her to care for pups.

 Mice homozygous for inactive fosB gene

ignore their pups.

 Funtional fosB gene usually activated in

hypothalamus by smell of newborn pups.

Female with active fosB









Female with inactive fosB



Pups

Oxt gene

 Mice missing Oxt gene cannot

produce oxytocin.

 Mutant male mice cannot remember

scent of females they recently

interacted with.

A gene “for”

 Remember that one gene does not code

for a behavior.



 One gene codes for one enzyme.



 Bita change in one enzyme can alter

numerous gene-environment interactions

and produce a detectable difference in the

phenotype.

A gene “for”

 The phrase “a gene for” some behavior is

shorthand for: a change in the gene leads

to a change in behavior.



 Allelse being equal, a change in a gene

can result in a detectable change in a

phenotype.

Evolution and behavioral

development

Garter Snake

In California, coastal and inland

populations of garter snakes differ in

diet.

Coastal garter snakes feed on banana slugs.

Inland populations eat other foods e.g. fish

and frogs.

 Is there a genetic basis to the behavioral

differences in diet preference?

Steve Arnold studied populations to see if

there were genetic differences between

them.



Brought pregnant females into lab and

reared babies in isolation.



Offered slug pieces to snakes.

Inland snakes usually ignored slugs, coastal

snakes usually ate it.

Then tested newborn snakes on response to

odors.



Offered snakes flavored cotton swabs,

counted number of tongue flicks made.

Coastal individuals responded much more

strongly to slug odor.

Arnold carried out heritability studies.



Found little variation within either population.



Preference for slugs within a population

largely fixed.

Crosses between populations produced

individuals with wide variation in response

to slugs.



Suggests differences between populations

have strong genetic component.

What is evolutionary basis for difference

Advantage to slug eating on coast is

between populations?

obvious.



Rare gene for eating slugs would spread

rapidly.

Artificial selection and

behavioral evolution

 Nest building in mice.



 Instarting population mice used 13-18

grams of cotton to line their nests.



 Carol Lynch selected for “high”, “low” and

“control” groups of mice.

15 generations amounts of cotton

 After

used by mice were:

 Controls 15g same as original population.

 High 40g

 Low 5g

Other examples of Artificial

Selection

 William Cade has selectively bred crickets

to sing rarely or almost continuously.



 In only two generations of artificial

selection Pulido et al. showed that the

timing of migration in European Blackcaps

could be delayed more than a week.

Artificial Selection

 Artificialselection experiments show that

(i) behavior is subject to selection and (ii)

populations contain sufficient genetic

variability to evolve rapidly.

Adaptability of behavioral

development

 As we have seen the development of

behavior such as singing can be strongly

influenced by environmental effects.

 It is important for development of behavior

to be resilient to disturbance so that

normal behavior can develop as often as

possible.

 Process of developmental homeostasis

reduces effects of disturbance.

Adaptability of behavioral

development

 Harlow’s “experiments” with Rhesus

monkeys showed that rhesus monkeys

entirely derived of contact with mothers

and “reared” by artificial surrogates gained

weight and grew normally but behaviorally

developed abnormally (BIG surprise!) and

were terrified of other monkeys if exposed

to them.

Adaptability of behavioral

development

 However, monkeys given even 15 minutes

contact a day with other young monkeys

developed essentially normally.

Adaptability of behavioral

development

 As adults, these monkeys interacted

normally with others unlike those

individuals which had no social contacts

as infants, which were withdrawn or very

aggressive.

Read Dawkins chapters 4 and 5 for next

Friday.



First exam is Wednesday February 22nd.

Developmental homeostasis in

human embryonic development

 We saw in studies of songbirds that adult

ability to learn and sing complex songs

was affected by food deprivation during

period of rapid nestling growth.



 Inhumans food deprivation of the mother

during pregnancy appears not to have

major effects on the fetus’ intelligence.

Developmental homeostasis in

human embryonic development

 Studies of children whose mothers were

food deprived during the Nazi transport

embargo of Holland in late WWII showed

that these children had comparable

intelligence scores and rates of mental

retardation as children whose mothers

were not food deprived.

Symmetry and attractiveness

 Manyorganisms are influenced by how

symmetrical other individuals are when

making mate choices.



 Asymmetries are believed to be caused by

problems in development and symmetry

thus signals an ability to overcome

developmental challenges.

Symmetry and attractiveness

 There is some evidence that humans

include symmetry in their ratings of an

individuals’ attractiveness, but data are not

conclusive and there is considerable

debate.

 Female brush-legged wolf spiders,

however, are significantly more likely to

mate with males whose foreleg hair tufts

are symmetrical than those who are not.



 Study was carried out using video images

of spiders that were identical apart from

the digitally manipulated foreleg tufts.

Polyphenism

 In many species multiple alternative

phenotypes occur in the same species (i.e.

distinctly different body types occur).



 These different phenotypes arise as a

result of environmental effects. The

environmental influence sends the

developing organism down one or another

distinct developmental pathway.

Developmental flexibility in Tiger

Salamnders

 Larvae live in ephemeral ponds.



 Most follow “normal” development and eat

small invertebrates.

But some become cannibals (bigger with

larger teeth) and eat smaller salamanders.

Normal form Cannibal

What factors affect decision to

become a cannibal?

 Ideas?

What factors affect decision to

become a cannibal?



 Relatedness of cannibal to others in pool.

 Density of salamanders

 Size distribution of salamanders

A salamander surrounded by lots of non-

kin can benefit by becoming a cannibal.



 Bygrowing faster it can escape from the

pond sooner.



 Developmental flexibility allows

salamander to adjust its development if

conditions are suitable, but not otherwise.

Behavioral flexibility

 Many animals choose among different

behavioral phenotypes depending on

environmental circumstances.



 For example, in many fish males adopt different

roles depending on their size and status. Large

males defend territories but smaller satellite

males act as sneakers darting in and releasing

sperm whenever the dominant male mates with

a female.

Behavioral flexibility in

Haplochromis burtoni

 In cichlid fish Haplochromis burtoni

territorial males are brightly colored and

satellite males are dull.



 Behavior is related to brain structure.

Satellite

male









Territorial

male

Behavioral flexibility in

Haplochromis burtoni



 GnRH (gonadotropin releasing hormone)

neurons in hypothalamus are 6-8 times

larger in territorial males than in satellites.



 GnRH neurons stimulate testes

development and aggressive behavior.

Behavioral flexibility in

Haplochromis burtoni

 Interestingly, GnRH size is variable.



male loses territory his neurons shrink

 If

and he becomes dull colored.



territory opens up, male enlarges

 If

neurons, switches to aggressive territorial

mode

Behavioral flexibility in

Haplochromis burtoni

 Unpredictable social environment favors

flexibility in Haplochromis.



 Neuronal flexibility allows males to adopt

best strategy for conditions.

Learning

 Learning major element in behavioral

flexibility. Ability to make use of

experience in adjusting behavior can

be selectively very advantageous.

Learning in Australian Thynnine

wasps

search for females based on

 Males

pheromones they produce.



 Orchids attract males using a similar

scent.



mimics female wasps appearance

 Orchid

too. When male lands and attempts to

mate he gets a surprise.

Male tries to mate with “female wasp”

on orchid, instead acquires a pollen sac.









Female wasp Fake wasp

Pollinia on

wasp’s back

Wasps don’t learn to avoid orchids in

general.



But, do learn to avoid orchids they have

visited before.

Learning in Australian Thynnine

wasps

 What do wasps learn?



 Orchid’s location or orchid’s scent?



 Speculation:If wasps could learn scent

differences how plants benefit from having

wasps revisit them?

Costs and benefits of learning

 Forlearning and flexible behavior to

spread by natural selection, benefits must

exceed costs.



are the ability to exploit the

 Benefits

environment more effectively.



 What are the costs?

Costs and benefits of learning

 Costs: Major cost is additional energy

required to make/maintain neuronal

tissue.

Example of cost:



West coast marsh wrens sing more songs

(100) than east coast marsh wrens (40).

Song system in brain weighs 25% more

in west coast birds.

Costs of large brain in humans

 In humans: Brain 2% of body weight.



 Butrequires 15% of body’s oxygen and

20% of energy.



 Other costs to large brains in humans?

Costs of large brain in humans

 Difficulty in giving birth.

Behavioral flexibility expensive.



Should only evolve when benefit

outweighs cost.

Clark’s Nutcracker seed-storing specialist.

Much better at remembering where

Something is located than other crows.

Not better at remembering colors, a non-

spatial task. Memory skills determined

by bird’s needs.

Intraspecific variability in

learning

 Behavioralflexibility does not only differ

between species.



 In species where males and females

experience different selection pressures,

differences in learning ability occur.

Spatial learning in voles

 Male meadow voles are polygynous.

Their home ranges are 4X larger than

those of females.



voles are monogamous. Males

 Prairie

and females have same size home ranges

Spatial learning in voles

 Spatiallearning abilities of voles was

tested in mazes.



 Malemeadow voles made significantly

fewer mistakes than female meadow

voles, but there was no difference

between the sexes in the performance of

male and female prairie voles.

Spatial learning in voles

 Male meadow voles have a large

hippocampus than females and this area

in the brain processes spatial information.



 However,the enlarged hippocampus only

develops during the breeding season.

Spatial learning in cowbirds

 Female cowbirds parasitize other birds

nests. They need to be able to remember

nest locations and monitor them over time.

Female cowbirds have a larger

hippocampus than males. No difference

between sexes in related, but non-

parasitic grackles and red-winged

blackbirds.

Operant conditioning

 Spatial learning not only behavior that has

clearly been shaped by selection.



 In operant conditioning (or trial and error

learning) an animal learns to associate an

action with its consequences.



 E.g. a rat pushes a lever and gets a food

pellet.

Operant conditioning

 Usuallya behavior and its consequences

must be closely linked in time for

conditioning to occur.



 However, in rats tasting novel foods

nausea that occurs several hours after

eating a food will be associated with that

food, which in future will be avoided.

Another example of operant conditioning is

that predators learn to recognize noxious

prey after tasting them.





How does warning

coloration benefit

animal that is tasted

if it is killed?

Does operant conditioning occur in

humans?


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