Week 7: Multiple Population Genetics: Dispersal and Gene Flow Flashcards

1
Q

What does gene flow depend on?

A

reproduction occurring

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2
Q

What is dispersal?

A

the movement of individuals between populatinos

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3
Q

What is migration?

A

periodic movements between specific geographic areas

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4
Q

In what 3 ways can we infer dispersal from genetics?

A
  1. Genetic differences between populations
  2. Population assignment tests
  3. Landscape Genetics
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5
Q

What methods can we use to measure dispersal/migration without genetics?

A
  • movement ecology (GPS)
  • Mark-recapture
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6
Q

What facilitates dispersal of individuals?

A
  • moving by themselves
  • wind
  • ocean currents
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7
Q

What main factor influences genetic differentiation between populations?

A

gene flow

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8
Q

What forces reduce genetic diversity in a population?

A
  • genetic drift and inbreeding
  • caused by barriers between populations, small population sizze
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9
Q

What 3 levels are F statistics measured at?

A
  • Fis = degree of inbreeding within a population (same as F/ INBREEDING COEFF)
  • Fst = genetic differentiation between subpopulation (FIXATION INDEX)
  • Fit = degree of inbreeding compared to all subpops (not as useful)
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10
Q

How do we calculate Fst?

A

Fst = (Ht-Hs)/Ht

Ht = expected total heterozygosity
Hs = expected subpop heterozygosity
Fst=0 –> no differentiation
Fst=1 –> complete differentiation

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11
Q

How do we calculate total expected heterozygosity (Ht) for finding Fst values?

A

Ht = He = (2pq)
- find allele frequencies and calculate 2pq

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12
Q

How do we find a subpopulation expected heterozygosity (Hs) for finding Fst values?

A

Hs = He (2piqi)

  • Find 2pq for each subpopulation separately
  • average 2pq between the two populations
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13
Q

What do we assume about subpopulations?

A

that there is a mutation-drift equilibrium

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14
Q

What data could challenge the assumption of a mutation-drift equilibrium in subpopulations?

A

microsatellite data (high mutation rate)

  • Fst are based on a priori guesses about population delineation
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15
Q

What does it mean if you find a low Fst value between two subpopulations?

A

High gene flow

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16
Q

What is implied if you find a high Fst value between two populations?

A

low gene flow, high genetic differentiation

17
Q

What are assignment tests used for?

A

to assign individuals to their most likely population of origin based on genotype

  • populations defined a priori, but can help determine dispersal
18
Q

In an assignment test, what can we assume if individuals are assigned to the populations we found them in?

A

no dispersal, correct identification of populations

19
Q

In an assignment test, what can we assume if individuals are assigned to populations other than the one we found them in?

A

dispersal between two subpopulations

20
Q

In an assignment test, what can we assume if individuals are assigned to a population that we did not define?

A

dispersed from a population we did not define a priori

21
Q

In an assignment test, what can we assume if all individuals are assigned to one subpopulation?

A
  • high gene flow or panmixia
  • other populations might not meaningfully exist
22
Q

When does dispersal not equal gene flow?

A

when migrants do not reproduce!
- ex. marbled murrelet - high dispersal, but migrants bred less than locals, so gene flow stayed low

23
Q

How can we infer dispersal from parentage/relatedness?

A

If offspring are in different populations than their parents!
- ex. pyrenean desman

24
Q

Why are populations hard to define a priori? (3 reasons)

A
  • home range and long-distance dispersal distances are unknown
  • dispersal could be based on something other than adult movement (ex. currents)
  • cryptic population structuring (barriers that are hard to observe, ex. reproductive behaviour)
25
What possible errors can be made in defining subpopulations a priori?
- pooling populations together - splitting a populations apart
26
What is a STRUCTURE analysis?
- Bayesian statistical analysis - incorporates prior information
27
What are the four inputs to a STRUCTURE analysis?
- Prior: how many populations you want to test for - Likelihood: probability distribution for our data - Computation/evidence: iterative MCMC - Posterior (what you solve for): probability distribution of parameter given the evidence (most likely K and assignments)
28
What is admixture?
gene flow between populations of the same species
29
What is introgression?
gene flow between populations of different species
30
What is indicated by a STRUCTURE analysis where most individuals are ~100% assigned to one population or the other?
admixture - ex separated in glacial refugia
31
What two methods are used in landscape genetics?
Neutral markers for gene flow/drift: - Isolation by distance - Isolation by resistance
32
What tools are used in landscape genomics?
Adaptive markers (natural selection and local adaptation) - Isolation by environment
33
What does the Mantel test do?
find correlation between different types of distance (genetic distance, geographic distance)