Evo Bio Midterm 2 Flashcards

(118 cards)

1
Q

Isogamy vs. Anisogamy

A

Isogamy: All gametes are the same size
Anisogamy: Gametes are size-dimorphic (only gametes of different sizes can fuse)

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2
Q

Anisogamy: Gamete Sizes

A

Large Gamete - Female
Small Gamete - Male
Large (Female) and Small (Male) Gametes - Hermaphrodite (most plants are likely hermaphrodites)

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3
Q

The Two-Fold Cost of Sex

A

Sexuals produce offspring at half the rate of asexuals
- each parent in sexual reproduction is responsible for 2 offspring
- the asexual parent produces an average of 4 offspring –> reproduction increases faster because not producing males that are required to reproduce sperm

In theory, asexuals should rapidly take over any population. However, the benefits of sex essentially prevent this from happening.

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4
Q

The advantages of sex (recombination)
–> the two hypotheses

A

1) Recombination facilitates the removal of deleterious mutations by selection
2) Producing offspring that differ from their parents is adaptive in variable environments

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5
Q

Accumulating beneficial mutations: Asexuals vs. Sexuals

A

Asexuals: Two beneficial mutants can be incorporated into the population only if the second occurs in a descendant of the individual in which it first occurred

Sexuals: On the other hand, in a sexual population, the various mutations can get into the same individual by recombination –> therefore, individuals can accumulate different mutations more quickly

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6
Q

Linked Loci and Selection

asexual reproduction

A

Linked loci interfere with each other’s response to selection

Without recombination, linkage facilitates the spread of deleterious mutations through a population (deleterious mutations can hitchhike with the beneficial ones)

Selection will find it difficult to pick the beneficial allele when its so close to the deleterious one

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7
Q

“Least loaded class”

A

Carrying the least amount of harmful mutations

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8
Q

(Asexual reproduction)
Why does the fittest clone eventually accumulate deleterious mutations?

A

In an asexual population, if the zero-mutation group is lost by chance, it’s gone forever –> no longer individuals that can possess 0 mutations

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9
Q

Muller’s Ratchet

A

The absence of recombination (especially in an asexual population), results in an accumulation of irreversible deleterious mutations

this muller is so ratchet that it can’t even recombine

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10
Q

Conditions that favor asexual reproduction

A

No deleterious alleles exist

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11
Q

How does sex break Muller’s ratchet?

A

Re-creates the zero-mutation class through recombination

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11
Q

Muller’s Ratchet: Genetic load

A

Decrease in fitness due to deleterious mutations increases over time

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12
Q

Conditions that favor sexual reproduction

A

Decrease in mutations
Can create offspring that don’t have deleterious alleles

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13
Q

Bet-hedging

A

When the environment is unpredictable, producing variable offspring increases the chance that some survive

sex is beneficial -> range of offspring produced (generates variation) -> will at least produce one offspring that will match the environmental background

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14
Q

Host-parasite coevolution

A

Parasites evolve to target common host genotypes.
Sex (recombination) produces rare genotypes. Therefore, offspring of sexuals less likely to be susceptible to parasites than asexuals

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15
Q

Sexual Selection

A

Differential reproductive success due to variation among individuals in success at getting mates

Other words: Selection that arises from differences in mating success

X-axis: Trait
Y-axis: Mating success

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16
Q

Sexual Selection and Natural Selection

A

Sexual selection often opposes natural selection because some traits increase mating success but decrease survival

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17
Q

What causes sexual selection?

A

One sex is more mate-limited than the other.

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18
Q

Operational sex ratio

A

The ratio of reproductively active males to females

When there are more reproductively active females, more males will get mates but not all females

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19
Q

Reproductive success: Heavily vs. lightly investing

A

Heavily Investing Parent –> resource/time limited
“female” -> intersexual selection –> choosy, can’t afford to mate with many

Lightly Investing Parent –> mate limited
“male” -> intrasexual selection –> compete for mates

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20
Q

Differences in mating success: strength of sexual selection

A

Larger differences in mating success among males –> stronger sexual selection in males

Smaller differences in mating success among females –> weaker sexual selection in females

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21
Q

When sexual selection is stronger in one sex, we can predict…

A

1) The sex subject to strong sexual selection will compete for mates [often but not always males]
2) The sex subject to weak sexual selection will be choosy (often but not always females)

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22
Q

Intersexual selection

A

Between-sex (female) choice
Differential mating success due to mate choice

1) pre-existing sensory bias
2) direct benefit of resources
3) indirect benefits “good genes hypothesis” -> ext. Hamilton-Zuk hypothesis

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23
Q

Intrasexual selection

A

Within-sex (male-male) competition
Differential mating success due to competition with members of the same sex

1) combat traits (alt. mating strategies can lead to disruptive selection)
2) sperm competition (race vs. raffle)
3) mating displays

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24
Combat traits
Used within-sex competition (intrasexual selection)
25
What sperm traits contribute to fertilization success?
Number of sperm (if sperm competition is a raffle) Sperm length (if sperm competition is a race)
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Sperm Competition: Prediction and Hypothesis
External fertilizers: Raffle Internal fertilizers: Race Internal fertilizers, sperm competition should drive the evolution of motility traits like length Internal fertilizers have longer sperm - Sperm length is a sexually selected trait driven by sperm competition
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What underlies preference for showy displays?
Pre-existing sensory bias Direct benefits: resource acquisition Indirect benefits: better genes for offspring
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Pre-existing sensory bias
Selection on avoiding predators, finding food, etc. make females more responsive to certain cues Female preference evolves first (for something other than mate choice) and male displays follow
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Sensory bias in Trinidadian guppies
Female preference for male orange coloration might be driven by pre-existing foraging preference for orange food
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Direct benefit of acquiring resources
In many species, males provide food, parental care, or some other resources If females can distinguish between males who provide more vs fewer resources, choosy females will do better than non-choosy females Larger gift (that male provides female) = longer copulation --> Longer copulation = more sperm transferred
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Indirect benefit of better genes for offspring
Displays may indicate genetic quality If individuals with better displays carry genes associated with higher fitness, the other sex will benefit from being choosy "good genes" hypothesis
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Indirect benefit of better genes for offspring: frog chirping example
Long-calling males produced offspring that grew faster and were more likely to survive than short-calling males
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Hamilton-Zuk hypothesis
Animals choose mates for genetic disease resistance, based on costly displays that only healthy individuals can afford to produce Individuals with showy displays were less likely to have parasites
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Cryptic Female Choice
Cryptic female choice (CFC) refers to post-mating female preferences that bias fertilization towards the sperm of specific males, or, alternatively, that favor or disfavor the zygotes produced with sperm of specific males
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Sexual dimorphism
Not all sexual dimorphism is caused by sexual selection In some cases, sexual dimorphism is the result of natural selection
36
Why cooperate with relatives?
Kin selection and the evolution of altruism
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Altruism
The actor suffers a cost; the recipient receives a benefit
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Why did altruism seem like a fatal problem for the theory of evolution?
Individuals with a certain trait will have a lower fitness. Therefore, natural selection should eliminate this trait, but it doesn't.
39
Kin selection
Selection could favor a trait that decreases an individual's fitness if it increases the survival and reproductive success of close relatives Why? Relatives share genes — the behavior of an individual toward others can influence the success of the actor's genes acts on INDIVIDUALS
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Reproductive altruism
An extreme form of altruism Some individuals forgo reproduction to help relatives reproduce Ex: Slime molds Although stock cells do not undergo reproduction, their altruistic behavior allows the spore cells to reproduce
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Individuals should act to...
Maximize their inclusive fitness!
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Inclusive fitness
Direct fitness + indirect fitness Direct fitness = an individual's own reproductive success Indirect fitness = additional reproduction by relatives made possible by an individual's actions
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What are the conditions under which altruistic behavior evolves?
Hamilton's rule The benefit to the recipient (B) is much larger than the cost to the actor (C) The recipient is a close relative (high r)
43
Hamilton's rule
Br - C > 0 B = benefit to the recipient r = relatedness between actor and recipient (0-1) --> the larger the R, the larger the weighted benefit C = Cost to the actor
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Calculating relatedness: the probability of identity by descent
Full siblings: r=1/2 Half-siblings: r=1/4 Cousins: r=1/8
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When are families likely to adopt another relative?
Adoptions only happened when the indirect fitness benefit outweighs the direct fitness cost. When the benefit is very high (Closely related) or if the cost is very low (mom doesn't have any many pups)
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How can cooperation evolve between non-relatives?
Reciprocity and Group selection/ multilevel selection
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Reciprocity
Actor incurs a fitness cost now in exchange for a future fitness benefit
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Group selection
A relationship between a group's phenotype and group fitness
49
Multi-level selection
Selection acting at multiple levels (on individuals and on groups)
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Group selection gradient
X-axis: group trait y-axis: group fitness
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Cooperation
If cooperators benefit their social groups, cooperation can increase in frequency in the population as a whole, even if it decreases in frequency within groups within groups, selfish individuals have higher fitness than cooperators but groups with more cooperators are more productive (in groups with more cooperators, all individuals have higher fitness) --> therefore, groups with cooperators produce more offspring selection favoring cooperators among cultures > selection against cooperators within cultures
52
What is life history evolution all about?
Tradeoffs How to allocate a finite pool of resources (eg survival, growth, reproduction)
53
Why do organisms age and die?
Mutation accumulation and antagonistic pleiotropy
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Mutation accumulation hypothesis
Late-acting deleterious mutations are weakly selected against The effective population size for late-acting mutations is smaller than for early-acting mutations --> selection is weaker on late-acting mutations and drift is stronger (also because Ne dies) Deleterious alleles should be at higher frequency than early-acting deleterious alleles
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The antagonistic pleiotropy hypothesis
Alleles conferring early benefits and late costs can be adaptive - More individuals will experience the early benefit than pay the late cost SELECTION favors an early-life benefit at the expense of a late-life cost Early life benefit helps organism to survive and reproduce, so when they experience a late-life cost, they have already reproduced,
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Extrinsic mortality
Non-age related mortality (eg predation) the rate of extrinsic mortality influences the rate of senescence
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Will individuals age more rapidly when extrinsic mortality is high or when extrinsic mortality is low?
When it's high! High extrinsic mortality favors early reproduction and weakens selection on aging. Low extrinsic mortality favors later reproduction.
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Infectious disease vs. non-communicable disease
infectious disease: an illness caused by a (micro)organism -> bacteria, fungus, virus, parasite non-communicable: an illness not caused by another organism --> heart disease, stroke, cancer, autoimmune disease, genetic disorder
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relative to their hosts, parasites and pathogens tend to have...
Larger population sizes, rapid generation times
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Virulence
The damage done by a parasite to its host
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Why are some pathogens more virulent than others?
Coincidental evolution hypothesis: pathogen virulence isn't a target of selection itself, but an accidental byproduct of selection on another trait (e.g. tetanus) Short-sighted evolution hypothesis: traits that enhance pathogen fitness within hosts decrease transmission between hosts Tradeoff hypothesis: Virulence can be favored by selection if killing its host increases the pathogen's chances of being transmitted (example of evolution favoring maximum virulence)
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Why would pathogens that are more likely to kill their host be more likely to transmit?
Rapid within-host reproduction = increased transmission A pathogen cannot reproduce inside its host without harming it --> to reproduce, pathogens steals energy and nutrients from the host, and/or produce toxic metabolic wastes
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Prediction with Tradeoff hypothesis
Selection favors parasites that reproduce more quickly within their hosts — until the parasites begin to harm the hosts so severely that they kill their host before transmission
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What does slower transmission favor?
Less virulent pathogens — cannot risk killing new host before finding another one to infect It is when pathogens have a shorter time to transmit, they are more virulent
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Transmission mode + Prediction
Direct transmission requires a mobile host Vector- or water-borne transmission does not Prediction: Vector-borne diseases should be more virulent than directly transmitted diseases
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What does the pathogen's fitness depend on?
Its transmission rate! Therefore, it doesn't care if they kill their host but only if it transmits to another host
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Why does antibiotic resistance (bacteria strains being resistant to antibiotics) decline when antibiotics aren't used?
Antibiotic resistance has a cost, so resistant strains have lower fitness (cost of resistance) than sensitive strains in the absence of the antibiotic
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Costs of resistance
Tradeoff between antibiotic resistance and another function (eg growth rate) Detectable as lower fitness of resistant pathogens when the antibiotic is not present --> loss-of-function mutations: the loss of function itself --> gain-of-function mutations: the expense of maintaining new genes and proteins
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If there's a cost to resistance, what will happen to the ratio of sensitive:resistant bacteria in the absence of antibiotic?
Sensitive strain will increase over evolutionary time
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Compensatory mutation
A subsequent mutation that eliminates the cost of resistance Therefore, over many generations, the sensitive strain should have no advantage anymore (eg a mutation that eliminates the tradeoff between resistance and growth rate) and the resistant strain will overcompete the sensitive strain
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Herd immunity
Some people cannot be vaccinated: Babies, pregnant women (some vaccines), immune-compromised people Herd immunity is the only thing protecting them
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Pathogens: Antibiotics vs. Vaccines
pathogens rapidly evolve resistance to antibiotics but not to vaccines vaccines: administered before infection, multiple immune responses, low effective population, broad immune pressure drugs: after infection, one site, high effective population, specific mechanism to be selected
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Why do pathogens rapidly evolve resistance to antibiotics but not to vaccines?
Timing of action antibiotics: administered therapeutically (large pathogen population size) vaccines: administered prophylactically (small pathogen population size) antibiotics: takes only 1 resistance mutation to evolve resistance to an antibiotic vaccine: takes many resistance mutations to evolve resistance to vaccines
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How to minimize antibiotic resistance?
Make antibiotics more like vaccines --> increase the number of mutations required to evolve resistance Minimize antibiotic use --> allow cost of resistance to eliminate resistant strains
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What is the unit of selection in a tumor?
A cell
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Cancer and Multicellularity
Cancer represents a breakdown of multicellular cooperation Multicellularity --> requires cooperation among cells for the development, maintenance and reproduction
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Four forces of evolution, applied to cancer
Mutation -> novel alteration of the genome Natural selection -> differences in fitness among cells with different phenotypes Gene flow (migration) -> the movement of cells between tissues (metastasis) Genetic drift -> random change in allele frequencies
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Proto-oncogenes vs. oncogenes
proto-oncogenes: genes that control the rate of cell division oncogene: mutated versions of proto-oncogenes that disrupt control of cell growth and division
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Larger-bodied animals and Cancer
Larger-bodied animals should be more likely to get cancer, because they undergo more cell divisions
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Cancer: Multi-level selection
Selection at the level of cells favors proliferation - Natural selection is short-sighted - Immediate fitness gains for cancer cells drive the evolution of increased cell division and metastasis Selection at the level of individual organisms favors cancer suppression
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Cancer and Viruses
Rather than viruses killing their host cells, they accelerate the rate of cell division to produce more viruses
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p-53: tumor-supressor protein
prevents cancer, but accelerates senescence deficient p53 activity --> survival will decrease because they are more likely to develop cancer elevated p53 activity --> most likely no cancer but mice suffer high tissue damage and end up dying early
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Genetic Drift and Cancer
Because tumor cell populations start out small, the fate of many mutations is governed by drift (random survival of that one cancer cell) --> means that many mutations that appear in tumors are neutral (unrelated to cancer phenotypes)
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Why is cancer so hard to treat?
The cancer cells are you! Like antibiotic resistance in bacteria, cancer cells that acquire mutations that allow them to resist chemotherapy grow faster than susceptible cancer cells
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Coevolution
Reciprocal evolutionary change between interacting species, driven by selection
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Why does coevolution often cause extremely rapid trait evolution?
Each trait is both the target and agent of selection
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Arms race
Coevolution between two species that causes escalating trait changes in both species More common with host-predator relationships Graph: Directional change in resistance
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Why can't every organism be highly resistant to something?
Because resistance is costly. E.g. Garter snakes and TTX Snakes that are less resistant have a high muscle force. Snakes that are more resistant have a low muscle force.
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Convergent evolution and toxins
Snakes that eat TTX-bearing amphibians around the world have convergently evolved TTX resistance.
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Red Queen coevolution
Common in host-parasite coevolution Parasites target common host genotypes Rare resistance alleles have a fitness advantage Parasite-host relationships
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Time shift experiments
Using time travel to test coevolutionary hypotheses Using resistance to today's organism in comparison to another organism back in time/present day Arms race: directional change in resistance --> snakes from further back in the past would be less and less resistant to today's newts Red Queen: cycles of resistance -> some snakes from the past would would be just as resistant to today's newt as snakes from the present
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Red Queen coevolution: Matching Alleles Model
When allele of parasite matches allele of host --> parasite can infect the host
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Parasite-Host allele graph
X-axis: Generation Y-axis: allele frequency No new resistance mutations forming in red queen -> fitness is a function of which allele is more common (makes this different from arms race)
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Red Queen coevolution with predatory-prey cycles in ecology
In ecology, changes in population size through time. Traits are (usually) treated as a fixed property of a species. In evolution, change in inherited traits (allele freq) of a population through time
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Plant traits and pollinators
Pollinators and flowers are remarkably well matched/plant traits have been shaped by coevolution with pollinators - Flower Color (red with hummingbirds/white with moths/bats) - Floral smell - Female mimicry in orchids (plant looks like a female fly so more males want to mate with it)
95
Is caffeinate nectar an adaptation to improve pollinator memory of floral rewards?
Maybe. But these data aren’t sufficient to test that hypothesis Caffeine also deters herbivores, because it’s bitter. Alternative hypothesis: Caffeine leaks into nectar. Its effect on pollinators is a byproduct of coevolution between plants and herbivores
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Mutualism
Benefits of mutualism also have a cost of providing goods and services (time, resources) Benefit must be larger than the cost
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Plant-microbe mutualisms
Model systems for studying mutualism's costs and benefits
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Microbial Mutualisms: Cost
Up to 20% of a plant's carbon budget goest to rhizobia (use light energy to convert carbon dioxide from the atmosphere into fixed carbon)
99
Under what condition (s) will a mutualism break down?
If the cost increases and the benefit decreases
100
In industrial agriculture, synthetic nitrogen fertilizer is added to the soil. Does nitrogen fertilizer influence the benefit or cost of the rhizobia mutualism for the plant?
It decreases the benefit of mutualism because the plant no longer needs the nitrogen these bacteria provide in order to grow
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Legume: rhizobia
Root nodule houses nitrogen-fixing bacteria called rhizobia (fertilizer factories) Nitrogen: benefit for legume / cost for bacteria Carbon: cost for legume / benefit for bacteria
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Indirect Benefit: Fischerian
Ignores viability (health of the partner) Ornamentation (trait to attract mates) evolves due to preference Preference persists as by-product "I find that attractive" "I'll make that then"
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Indirect Benefit: Condition Dependent
Only high viability males can make ornamentation Females want healthier males
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Indirect Independent
Not related to viability Different from Fischerian because female preference evolves independently
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Hill-Robertson Interaction
Deleterious mutation link to another locus
106
As genetic relatedness increases...
Benefit to cooperation increases
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Viruses + Solution
Transmit more --> But... if it doesn't replicate, it'll run out of copies fast Replicate more --> But...then it might kill the host and cannot transmit 1) Don't transmit using hosts: use water or vectors (can replicate more) 2) Replicate as much as possible without killing the host tradeoff hypothesis x
108
Bacteria: Pros and Cons of Resistance
If no resistance: Pro: No costs. Con: You probably die. If resistance: Pro: You don't die. Con: You take a fitness cost (this is why resistance goes down without antibiotics). They can evolve to compensate. Phage therapy takes advantage of this.
109
Halfwerk et al. 2018 "Tungara frogs paper"
Male frogs in urban environment had more conspicuous (standing out) calls Less predators -> less negative selection Less mating -> more desperate Females were more attracted to urban frog calls -> urban frogs were also flexible between environments
110
Jones and Ratterman 2008
Mate choice is essential to mechanisms of sexual selection Bateman gradient x-axis: # of mates y-axis: # of offspring male: directional line (competition, needs more mates for reproduction isn't resource-heavy, doesn't care about good quality offspring) female: plateau (resource-heavy, won't produce as many offspring because investing)
111
Kramer and Meunier
Mainly address controversies between group selection and kin selection
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Tarpy et al. 2004
Test of group vs. kin selection: 2 mechanisms by how new queens are made Queen Rearing: workers could favor related queens, KIN SELECTION "nepotism" Queen Elimination: best queen wins = best for entire hive, MULTILEVEL SELECTION Findings: No, worker bees prioritize best-quality queen regardless of relatedness --> supports broader arguments for multi-level selection
113
Eusociality: 3 Major Pillars
Mutual Care of Offspring, Overlap of Generations, Reproductive Division of Labor
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