IV. POPULATION GENETIC MODELS: UNDERSTANDING THE MODELS,
PRACTICE PROBLEMS (See Freeman and Herron (2001) Chapter 5 and
the lecture notes on Hardy-Weinberg Equilibrium
and the mathematical model of natural selection)
Terms to know: allele frequency, genotype frequency, Hardy-Weinberg
equilibrium, absolute fitness, relative fitness, average population fitness,
natural selection, gene, locus, allele, homozygote, heterozygote, genetically
dominant, genetically recessive.
Questions:
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The Hardy-Weinberg Equilibrium model is a model of no evolution.
Why is it important to know this model in order to understand evolution?
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What are the five assumptions about a population that must be true for
the population to be in Hardy-Weinberg Equilibrium? For each assumption,
describe what happens if the assumption is NOT true of a population, and
explain why this result occurs.
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Are the assumptions of Hardy-Weinberg Equilibrium typically met in populations?
Why/why not?
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In order to model natural selection, the mathematical model of natural
selection must be modelling all of Darwin's four postulates. What
are Darwin's four postulates, and how does the mathematical model include
each?
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A population of pocket gophers is in Hardy-Weinberg equilibrium with respect
to an enzyme locus, ADH, at which there are two alternate alleles, A1 and
A2. The frequency of allele A2 in the population is 0.6. What are
the frequencies in the population of the three possible genotypes at this
locus? Suppose that this population has 13,000 individuals
in it (this is a large enough number so that it is effectively infinite,
meeting the assumptions of Hardy-Weinberg Equilibrium.) How many
individuals have each genotype?
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The frequency of a recessive allele at a locus with two alleles in an infinitely
large population of spadefoot toads is currently 0.09. There is no
selection at this locus, toads mate at random, this population is completely
isolated from all other populations, and no mutations are occurring at
this locus.
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What will the frequency of the recessive homozygote be in the next
generation?
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Over a long period of time, what will happen to the frequency of
the recessive allele?
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In house cats, the presence of white splotches is coded for by a dominant
allele S; the recessive allele s codes for no white splotches. In
a large feral house cat population, you find that 5/9 of the cats have
white splotches. Assuming random mating, no natural selection on
white splotches, and no mutation or gene flow, what proportion of the cats
in the population are heterozygous at the S locus? Will this proportion
change from generation to generation? Why /why not?
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In a randomly mating population of 25,000 (large enough to be considered
infinite for the purposes of the assumptions of the models; assume this
population size remains constant throughout the generations described in
this question) newts there is an enzyme locus with two alleles, F and S,
at which the three different genotypes have equal fitness.
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If the frequency of the FF genotype is currently 0.16, what is the frequency
of the SS genotype in this generation? What will be the frequency
of the SS genotype in the next generation? Assuming the population
stays the same size, how many individuals in the next generation will have
the SS genotype?
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In the same newt population, a locus affects the structure of the skin
of developing newt larvae as follows: HH and Hh individuals have
skin that resists drying out, while hh individuals have skin that tends
to dry out. Further, Hh and hh individuals have skin that is not
harmed by ultraviolet light, while HH individuals have skin that IS harmed
by ultraviolet light. The result is that Hh individuals avoid drying
out and are not harmed by ultraviolet light, so that they have the highest
fitness. HH individuals survive 3/4 as well as do Hh individuals;
hh individuals survive 1/3 as well as do Hh individuals. The allele
frequency of h at the start of a generation is 0.95. What will the
allele frequency of h be at the start of the next generation?
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Consider a different newt population. The conditions are all the
same as they were for the population in part (b), except in this population,
the allele frequency of h at the start of a generation is 0.05. What
will the allele frequency of h be at the start of the next generation?
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What do you think will happen to the frequencies of H and h in these newt
populations over time (will either become fixed? lost? will either
increase? decrease?).
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In a population of beavers, three genotypes, BB, Bb, and bb, have different
probabilities of survival to reproductive age that result in them having
relative fitnesses of .5, .8, and 1.0, respectively. In the gametes that
produce one generation, the frequency of B = the frequency of b.
Natural selection resulting from differences in survival to reproductive
age is the only form of evolution occurring in this population.
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What will the allele frequencies of B and b be in the adults of this generation?
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What will the allele frequencies of B and b be in the gametes that produce
the next generation?
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What will the allele frequencies of B and b be in the adults of the next
generation?
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In the same population of beavers, at the T locus, individuals with the
three genotypes TT, Tt, and tt have equal probabilities of surviving and
reproduce equally well. This generation, 90% of the adults have the
tt genotype. What are the allele frequencies of T and t in this population
this generation? What will they be in adults of the next generation?
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Consider two genes in a large, randomly mating population of turtles with
no movement of individuals in and out of the population and no mutation.
The two alleles at one gene, L and M, do not affect fitness. The
two alleles at the other gene, T and t, do affect fitness -- they affect
the thickness of turtle shells, and the degree to which they are protected
from predation. TT individuals have thick shells, which repel predators,
and survive best. Tt individuals have medium shell thickness and
survive 88% as well as do TT individuals. tt individuals have thin
shells and are easy for predators to eat; they survive only 14% as well
as do TT individuals.
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In a population of ADULT turtles, the frequency of individuals with the
MM genotype is 0.06. Calculate the frequency of individuals with
the LM genotype.
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In a population of gametes at the start of a generation, the frequency
of the t allele is 0.23. Calculate the frequency of zygotes with
the Tt genotype.
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Continuing from part (b), calculate the frequency of the adults that survive
from the zygotes that have the Tt genotype.
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Continuing from part (c), calculate the frequency of the t allele in the
gametes that will produce the next generation
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In a large, randomly mating population of giraffes with no movement of
individuals in and out of the population
and no mutation, the two alleles at one gene, A and a, do not affect
survival or reproduction of the giraffes. The two alleles at the
other gene, S and B, do affect survival to adulthood by affecting the degree
to which giraffes are subject to parasitism by ticks and biting flies.
BB individuals have bitter blood, which repels parasites, and survive best.
SB individuals have neutral tasting blood and survive 80% as well as do
BB individuals. SS individuals have sweet blood and attract parasites;
they survive only 4% as well as do BB individuals.
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In a population of ADULT giraffes, the frequency of individuals with the
AA genotype is 0.04. Calculate the frequency of individuals with
the Aa genotype.
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In a population of gametes at the start of a generation, the frequency
of the B allele is 0.14. Calculate the frequency of zygotes with
the SB genotype
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Continuing from part (b), calculate the frequency of the adults that survive
from the zygotes that have the SB genotype.
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Continuing from part (c), calculate the frequency of the B allele in the
gametes that will produce the next generation
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In a large population of an annual wild pea species, height is controlled
by a single locus; HH and Hh individuals are tall, while hh individuals
are short. Because the local environment is very windy, tall
plants tend to get broken and survive to reproduce only half as well as
well as do short plants. Mating is random with respect to height
and there is no immigration or emigration.In a population of 21,000 (large
enough to be considered infinite for the purposed of the Hardy-Weinberg
Equilibrium and natural selection models; assume this population size remains
constant through the generations described in this question) adult pea
plants that successfully reproduce after natural selection through differential
survival has occurred, there are 7,000 HH individuals, 7,000 Hh individuals,
and 7,000 hh individuals.
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What will be the frequency of the H allele in the gametes (sperm, in pollen,
and ovules) that will unite to make up the next generation?
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What will be the genotype frequencies of HH, Hh, and hh in the seeds that
are formed to start the next generation? How many seeds will there
be with each genotype?
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What will be the genotype frequencies of HH, Hh, and hh in the adults that
develop from these seeds and survive to reproduce? How many adults
will there be with each genotype?
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Over a long period of time, what do you expect to happen to the H and h
alleles in this population?
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A large population of grass occurs in an area with two distinct kinds of
soil. Some patches of soil contain heavy metal ions, others do not.
The genotypes at the S locus determine how well grass plants survive in
the different soil types: SS individuals survive best in heavy metal soils,
ss individuals survive best in normal soils, and Ss individuals do not
survive very well in either soil. Grass seeds are dispersed by the
wind to different soil types; because normal soil is most common, ss individuals
have the highest survival, and a relative fitness of 1. SS individuals
survive next best, having a relative fitness of .75. Ss individuals
have a relative fitness of .25.
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In this population of grass, the allele frequency of S at the start of
a generation is 1/2. What will the allele frequency of S be at the
start of the next generation?
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In a different large population of grass, the fitnesses of the SS, Ss,
and ss genotypes are the same as in the first population. However,
in this population, the allele frequency of S at the start of a generation
is 0.90. What will the allele frequency of S be at the start of the
next generation?
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What do you think will happen to S over time in the first population?
Will the same thing happen in the second population? Why/ why not?
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In a very large population of crayfish in a cold, mountain stream, there
are two possible alleles at the locus of enzyme D. One form of this
enzyme, coded for by allele D, functions more effectively at cold temperatures
than does the alternate form, d. As a result, DD and Dd individuals
survive better than do dd individuals; the absolute fitness of DD and Dd
is 3, the absolute fitness of dd is 2/3. This population is isolated
from other populations; individuals mate at random with respect to the
D locus. In a population of 10000 fertilized crayfish eggs, there are 2000
dd individuals.
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What is the frequency of D in the fertilized egg population?
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What are the relative fitnesses of the three possible genotypes?
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What is the frequency of D expected to be in the population of gametes
produced by this population of fertilized eggs (once they grow up and reproduce).
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Go back over each of the questions in this section in which natural selection
was modeled and identify the mode of selection as one of the following:
dominant has highest fitness, recessive has highest fitness, fitness codominance,
heterosis (overdominance), or underdominance (negative heterosis)