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Reebop Populations

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Evolutionary biologist John Endler studied guppy populations in Trinidad. He noticed wide color variation in guppies living in different streams. ... – PowerPoint PPT presentation

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Title: Reebop Populations


1
Reebop Populations
2
Do Reebops evolve?
  • Based on what we already know about Reebop
    genetics and reproduction, do you think that
    Reebops could evolve? Why?
  • Under what conditions might Reebops evolve? Why?
  • How would we know if they did evolve?

3
Do Reebops Evolve?
  • A drought has forced our Reebop population to a
    new location.
  • The vegetation in this new location is not as
    tall as before.
  • The tails of the straight-tailed Reebops stick
    above the vegetation, and they are more visible
    to predators.
  • All of the straight-tailed Reebops are eaten
    before they can reproduce.

4
So, DO Reebops Evolve?
  • Soon, we are going to find out if Reebops evolve
    under these new conditions.
  • In a scientific inquiry, we must know what data
    we should gather to help us answer our question.
  • So, what data can we gather to provide evidence
    of evolution?

5
Measuring Evolution
  • To help us decide what data to gather, lets look
    at a definition for biological evolutionA
    process that results in heritable changes in a
    population spread over many generations.
  • ProblemThis definition does not suggest a way
    to measure these heritable changes.

6
Measuring Evolution
  • Does this definition for biological evolution
    help us decide what to measure?Any change in the
    frequency (proportions) of alleles within a gene
    pool from one generation to the next.
  • Gene Pool all of the genes in all of the
    individuals in a breeding population.

7
Measuring Evolution
  • To decide if a population is evolving, we can
    measure change in the frequency of alleles within
    a gene pool from one generation to the next.
  • But, to measure a change, we must first know
    where we started

8
Measuring Evolution
  • Lets focus on the frequency of the tail trail
    allelesT and t.
  • The parent Reebops wereheterozygous (Tt) for
    this gene.
  • What percentage of alleles in the parent
    generation gene pool were t? What percentage
    were T?

9
Measuring Evolution
  • If all parent Reebops were Tt,50 of the gene
    pool will be T and50 of the gene pool will be
    t.
  • In other words, in the parent generation, the
    frequency of T is 50 and the frequency of t is
    50.

10
Measuring Evolution
  • Remember breeding the Reebops?
  • Were the frequencies in the gene pool of the F1
    generation still 50 T and 50 t ?
  • Our Punnett square can provide the answer!

11
Measuring Evolution
Imagine 100 F1 offspring
T
t
25 are TT 50 copies of T
Tt
TT
T
50 are Tt 50 copies of T
tt
Tt
t
25 are tt 0 copies of T
Population has 100 copies of T
12
Measuring Evolution
Imagine 100 F1 offspring
T
t
25 are TT 0 copies of t
Tt
TT
T
50 are Tt 50 copies of t
tt
Tt
t
25 are tt 50 copies of t
Population has 100 copies of t
13
Measuring Evolution
F1 Population has 100 copies of T
F1 Population has 100 copies of t
Frequency of T is still 50
Frequency of t is still 50
14
Measuring Evolution
  • Now we know that the starting frequency of T is
    50 and the starting frequency of t is 50.
  • Without selection pressure, these frequencies did
    not change from the parent generation to the F1
    generation.
  • If we see changes in these frequencies over
    generations, we are seeing evidence of evolution.

15
Measuring Evolution
Lets apply some selection pressure to the tail
trait and see what happens to our allele
frequencies
16
Stop for Reebop Population activity.
17
Did Our Reebop Population Evolve?
  • What happened to the frequency of T?
  • What happened to the frequency of t?

18
Did Our Reebop Population Evolve?
Biological Evolution Any change in the frequency
of alleles within a gene pool from one generation
to the next.
19
Did Our Reebop Population Evolve?
T (.73)
t (.27)
T (.50)
t (.50)
T (.73)
TT (.73)2
Tt (.73)(.27)
T (.50)
TT (.50)2
Tt (.50)(.50)
t (.27)
tt (.27)2
Tt (.73)(.27)
t (.50)
tt (.50)2
Tt (.50)(.50)
TT (.73)2 .53 Tt 2(.73)(.27) .40 tt
(.27)2 .07
TT (.5)2 .25 Tt 2(.5)(.5) .50 tt (.5)2
.25
20
Quick Think Time
  • If selection pressure against tt continues, will
    the t allele ever disappear from the population?
  • If no selection pressure against Tt individuals
    exists, the t allele will persist in the
    population.

21
A New Population
22
John Endlers Guppies
  • Why do these guppies look so different?

23
John Endlers Guppies
  • Evolutionary biologist John Endler studied guppy
    populations in Trinidad.
  • He noticed wide color variation in guppies living
    in different streams.
  • Endler also observed differences in the
    distribution of guppy predators and in the color
    of gravel in different locations.
  • He found that male guppies are brightly colored
    in streams with few predators, but are drably
    colored in streams with many predators.
  • He also found that females prefer brightly
    colored males.

24
When Do Populations Evolve?
  • Remember how the gene pool frequencies of the T
    and t alleles stayed 5050 from the parent
    generation to the F1 (with no selection)?
  • It turns out that gene pool frequencies dont
    change (evolution does not occur) unless certain
    factors cause them to change.
  • Think of a similar idea in physicsan object at
    rest stays at rest until a force acts on it.

25
When Do Populations Evolve?
  • These factors cause allele frequencies in
    populations to change
  • Mutations
  • Non-random mating
  • Natural selection (you knew that!)
  • Migration
  • Isolation

26
No Evolution?
  • In the early 1900s, Godfrey Hardy and Wilhelm
    Weinberg used mathematical analysis to developed
    a set of rules now called the Hardy-Weinberg Law.
  • These rules describe a population that is not
    evolving.
  • Another way to say that a population is not
    evolving is to say it is in Hardy-Weinberg
    equilibrium.

27
The Hardy-Weinberg Law Says
  • If these conditions are met
  • No mutation
  • No natural selectionall survive and reproduce
    equally
  • Infinitely large population, so no genetic drift
    (deviations due to chance)
  • Random mating
  • No migration in or out of the population
  • Then the frequency of alleles does not change
    over time.

28
Hardy-Weinberg Equilibrium
  • We say that a population meeting these conditions
    is in Hardy-Weinberg Equilibrium.

29
Hardy-Weinberg Equation
If a population is in equilibrium, you can
calculate allele frequencies and genotype
frequencies using the Hardy Weinberg equation.
30
Hardy-Weinberg Equation
T (p)
t (q)
If we call the frequency of the dominant allele
p and the frequency of the recessive allele
q, then TT (p)2 Tt 2(p x q) tt (q)2
TT (p)2
Tt (p x q)
T (p)
tt (q)2
Tt (p x q)
t (q)
And(p)2 2(p x q) (q)2 1
31
Hardy-Weinberg Equation
Ta daThe Hardy-Weinberg Equation (p)2 2(p x q)
(q)2 1
The Hardy-Weinberg equation tells us If the
frequencies of the alleles in a population remain
the same, the ratio of genotypes will remain the
same from generation to generation.
32
Using Hardy-Weinberg
  • Albinism is a rare homozygous recessive (aa)
    trait.
  • The most characteristic symptom is a deficiency
    in the skin and hair pigment melanin.
  • Albinism occurs among humans as well as among
    other animals.
  • The average human frequency of albinism in North
    America is about 1 in 20,000.

albino gorilla Snowflake
33
Using Hardy-Weinberg
  • Referring back to the Hardy-Weinberg equation (p2
    2pq q2 1), the frequency of homozygous
    recessive individuals (aa) in a population is q2.
  •  
  • Since we know that the 1 in 20,000 people with
    albinism are aa, the following must be true
  • q2 1/20,000 .00005

34
Using Hardy-Weinberg
  • Take the square root of both sides of the
    equation
  • q2 .00005 q .007
  • So, the frequency of the recessive albinism
    allele (a) is .007 or about 1 in 140.
  • Knowing (q), it is easy to solve for (p)
  • p 1 - q p 1 - .007 p .993
  • So, the frequency of the dominant allele(A) is
    .99293 or about 99 in 100.

35
Using Hardy-Weinberg
  • Plug the frequencies of p and q into the
    Hardy-Weinberg equation
  • p2 2pq q2 1
  • (.993)2 2(.993)(.007) (.007)2 1
  • .986 .014 .00005 1
  • p2 predicted frequency of AA  .986 98.6
  • 2pq predicted frequency of Aa  .014 1.4
  • q2 predicted frequency of aa  .00005 .005

36
Using Hardy-Weinberg
  • With a frequency of .005 (about 1 in 20,000),
    persons with albinism are rare. 
  • Heterozygous carriers for this trait, with a
    predicted frequency of 1.4 (about 1in 72), are
    far more common. 
  • The majority of humans (98.6)probably are
    homozygous dominantand do not have the albinism
    allele.

37
Using Hardy-Weinberg
  • You can find an interactive example of using the
    Hardy-Weinberg equation at http//www.phschool.com
    /science/biology_place/labbench/lab8/allfreq.html.
  • Lab Bench Activity Estimating Allelic Frequency

38
Not In Equilibrium?
  • Many populations are not in Hardy-Weinberg
    equilibrium.
  • So how is the Hardy-Weinberg equation useful
    then?
  • The model of a population in equilibrium allows
    us to see if data from other populations conforms
    or deviates.
  • Deviations from the model equilibrium population
    help us identify evolutionary processes.

39
New Species
  • Imagine a flood washed some Reebops across a
    river where they became permanently isolated from
    the original population.
  • Not only was the grass shorter (too bad for the
    tts), but the environment was different in a lot
    of other ways.
  • Over many, generations, the gene frequencies for
    tail shape changed. In a similar way, the gene
    frequencies for lots and lots of other genes also
    changed.
  • Mutations of some genes added new alleles that
    didnt even exist in the original population.

40
New Species
  • Finally, they didnt look like the original
    Reebops, nor were they able to mate with them on
    the rare occasions when they did come into
    contact.
  • They had evolved into a new species.
  • The accumulation of genetic differences between
    populations in different habitats over many
    generations is what gives rise to new species.

41
Can Diseases Be Good?
  • Some human genetic diseases result from
    inheriting two recessive alleles.
  • Without modern medical treatment, most of these
    diseases are fatal in childhood. So why do the
    alleles for these diseases persist?
  • We know that some recessive alleles will remain
    in the population as long as heterozygotes are
    not selected against.
  • But in some situations, the percentage of the
    recessive allele actually rises in the
    population, even though the homozygous recessive
    is often fatal.
  • How can that happen?

42
Can Diseases Be Good?
  • Some of these diseases actually provide an
    advantage to heterozygotes over the homozygous
    dominant individuals.
  • When carriers of an allele have advantages that
    allow a detrimental allele to persist in a
    population, balanced polymorphism is at work.
  • This form of polymorphism often entails
    heterozygosity for an inherited illness that
    protects against an infectious illness.
  • Lets look at some examples

43
Can Diseases Be Good?
  • Sickle Cell Disease causes anemia, joint pain, a
    swollen spleen, and frequent, severe infections.
    Carriers (heterozygotes) are resistant to
    malaria, an infection of the blood cells by the
    parasite Plasmodium falciparum.
  • People who inherit one copy of the sickle cell
    allele have red blood cell membranes that do not
    admit the parasite.
  • In East Africa, during a period when land being
    cleared for cultivation produced an ideal
    mosquito habitat, the frequency of the sickle
    cell allele rose from 0.1 percent to 45 percent
    in 35 generations.

44
Can Diseases Be Good?
  • Mutation Story

45
Can Diseases Be Good?
  • Phenylketnonuria (PKU) is an error of metabolism
    in which a missing enzyme causes the amino acid
    phenylalanine to build up, with devastating
    effects on the nervous system unless the
    individual follows a restrictive diet.
  • Carriers (heterozygotes) have slightly elevated
    phenylalanine levels. Physicians have observed
    that women who are PKU carriers have a much
    lower-than-average incidence of miscarriage.
  • One theory is that excess phenylalanine somehow
    inactivates a poison, called ochratoxin A, that
    certain fungi produce and that is known to cause
    spontaneous abortion.

46
Can Diseases Be Good?
  • Tay-Sachs is a fatal disease of the central
    nervous system. Babies lack an enzyme called
    hexosaminidase A (hex A) necessary for breaking
    down certain fatty substances. These substances
    build up and gradually destroy brain and nerve
    cells. Death occurs by age 5.
  • In Eastern European Jewish populations, up to 11
    percent of the people are Tay-Sachs carriers.
  • During World War II, Tuberculosis was rampant in
    Eastern European Jewish settlements. Often,
    healthy relatives of children with Tay-Sachs
    disease (probably heterozygotes) did not contact
    Tuberculosis, even when repeatedly exposed.

47
Defining Biological Evolution
  • The changes in populations that are considered
    evolutionary are those that are inheritable via
    the genetic material from one generation to the
    next.
  • Biological evolution may be slight or
    substantialit embraces everything from slight
    changes in the proportion of different alleles
    within a population (such as those determining
    blood types) to the successive alterations that
    led from the earliest proto-organism to snails,
    bees, giraffes, and dandelions.
  • Douglas J. Futuyma in Evolutionary Biology,
    Sinauer Associates 1986
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