Short-term measures: "Life Table" parameters
rate of instantaneous increase (r) of a phenotype
recall logistic
equation:
dN/dt = rN = rN (K-N)
/ K
where K = carrying capacity
net reproductive rate: exp(r)
= er
r is "compound interest" on N
replacement rate (RO):
lifetime reproductive output
~ er(at low density)
components of fitness:
traits
that contribute to survival &
reproduction
Ex.: survivorship (expected survival time)
fecundity (# offspring at age x)
Adaptationis
the phenotypic consequence for populations of natural selection on individuals
[cf.
adjust / acclimate]
Phenotypic
traits that change as a result of selection
are sometimes referred to as "adaptations"
or "adaptive characters"
Life table analysis: survivorshipand fecundityvary with age
lx
= prob. of survival from birth to age
x
(cumulative)
survivorship = probability of survival
to age x+1 from age x
mx
= fecundity (# offspring) at age x
L
then
(lx)(mx) exp(-rx) = 1
(in a stable population,
x=1
where L = life expectancy)
L
Ro=
(lx)(mx)
replacement rate
erat
low density
x=1
This equation
is a discrete solution to the continuous logistic equation
Consider a population with two
demographic
phenotypes:
These phenotypes
correspond to two reproductive 'strategies
iteroparous
strategy:
offspring produced over several seasons
semelparous
strategy:
offspring produced all in one season
A survivorship
and fecundity schedule will compare their life histories
life table parameters can be measured experimentally
Under 'typical'
environmental conditions, survivorship is 50% / year:
both strategies produce 2 young / female / lifetime
=> both phenotypes are equally 'fit' [and N is stable]
In 'good
times', survivorship increases to 75% / year:
iteroparous strategy produces 4 young / female / lifetime
semelparous strategy produces 3 young / female / lifetime
=> iteroparous phenotype is 'more fit' [and N is increasing]
In 'bad
times', survivorship decreases to 25% / year:
iteroparous
Ro = 0.72, semelparous Ro
= 1.00
=> semelparous phenotype is 'more fit' [and N is decreasing]
=> Population phenotypes will adapt to changing conditions
In a favourable
environment, K increases:
e.g.,
productivity of meadow increases
iteroparity more advantageous, population density increases
In an unfavourable
environment, r increases:
e.g.,
severity of winter highly variable
semelparity more advantageous, early reproduction favoured
K-strategy:
maintain population size N close to K
long-lived,
reproduce late, smaller # offspring, lots of parental care
E.g.,
many bird species, primates (including Homo)
r-strategy:
maximize growth potential
r
short-lived,
reproduce early, larger # offspring, little parental care
E.g.,
most invertebrates, some rodents
We can extend single-locus
multilocus
quantitative models
p2:2pq:q2
W0,W1,W2
Mendel's Laws & H-W Theorem
normal
distribution fitness
function
high heritability
Variation can be quantified
mean
standard deviation: ![]()
![]()
variance:
2
coefficient
of variation (CV)
= (
/
)
x 100
CV removes
size effect when comparing variance:
Ex.: Suppose X = whale length
Y
= tail width
X = 100
1.0
versus
Y = 1.0
0.1
CV of X = 1% CV
of
Y = 10%
Y is more variable, though
X
is larger
Quantitative
variation follows "normal distribution"
(bell-curve) iff
Multiple loci are involved
Each locus has about the same effect
Each locus acts independently
[interaction variance (see below) is minimal]
Variation has two sources: genetic
(
G2) &
environmental
(
E2)
variance
phenotypic variance
P2
=
G2
+
E2
+
GxE2
additive variance
A2
=
G2
+
E2
heritability
h2 =
G2/
A2
=
G2
/ (
G2 +
E2)
"heritability in the narrow sense": ignores
GxE2
interaction variance:
Identical genotypes produce different phenotypes in different
environments.
Ex.: same breed of cows produces different milk yield on different
feed
Artificial breeding
indicates that
organismal variation is highly heritable
ex.:
Darwin's
pigeon breeding experiments
Artificial selection
on agricultural species
Commercially useful traits can be improved by selective breeding
IQ scores in Homo: h2
0.7
[But: IQ scores improve with education:
GxE2
is large]
Offsrping / Midparent correlation
For many traits in many organisms:
CV = 5 ~ 10 %
h2 = 0.5 ~
0.9
[Read "Suggestions for using the Website" for used in this course]
Fitness function
expresses relationship between
genotype & fitness
Function is a continuous
variable, rather than discrete values for W0,
W1,
& W2
=> Most traits vary & are heritable.
Many traits
do
respond to 'artificial' selection.
Many traits
should
respond to 'natural' selection.
=> To demonstrate & measure Natural
Selection,
we must
show experimentally that heritable variation has consequences for fitness
<=
"Form
& Function":
Organisms typically exhibit engineering criteria of "good
design"
Beak
variation in Hawai'ian honeycreepers (Drepaninae)
Beak type matches food type
Aerodynamics
of bat & bird flight
Slow fluttering bats versus fast soaring birds
Wings match aerodynamic principles
Assumption: Form & Function affect survival & reproduction
Persistence:
"Estimated time to extinction"
Are long-lived lineages "better adapted"?
Multituberculata
versus modern mammalian orders (3D
animation)
Order persisted more than twice
as long as any extant order
Ultimately outcompeted by Rodentia
Chondrichthyes
(sharks & rays) versus Teleosts
Body form is unchanged in 400 MY
Class is about as diverse now as at anytime in last 250 MY
Agnathan
orders [Hagfish & Lampreys] versus gnathostome orders
Descendants of Ostracoderms, 500 MYBP (million
years before present)
Jawlessness works [ectoparasitism is probably secondary]
"Adaptive characters" cannot be separated from the organisms that bear them
Ex.: We typically say "Hair & feathers evolved from scales".
But: It is more accurate to say:
"Reptiles (with scales) evolved into mammals (with hair) and birds
(with feathers)."
[and this isn't completely accurate either]
|
Agnaths (scaleless)
|
Ex.: In a mammalogy class, we might say
"The carnassial pair evolved from
the P4/M1
combination."
But: it is more accurate to say
"Carnivorous mammals evolved from insectivorous
ancestors.
The carnassial pair is adapted for slicing meat."
Quantitative
trait distribution can be described as a bell curve
with a particular mean & variance:
What happens to this distribution under Selection?
[See Futuyma Fig. 13-02
and Freeman & Herron (1998)
for alternate presentations]
(1) Directional Selection
Fitness
function has constant slope:
Trait mean
shifted towards favored phenotype
trait variance unaffected
In single-locus
models, the limit of selection is
Elimination
of variation by fixation of favored allele
In quantitative models,
rate is limited by
substitutional
genetic load:
"cost" of replacing non-favored allele (
"intensity" of selection)
"Soft"
selection
Mortality is density-dependent
In 'real' populations: N(after)
N(before)
Survivorship is proportional to fitness up to K: more realistic
Selection will affect recruitment to next generation
Ex.: If the first-born dies of malaria, s/he will be replaced.
More births occur such that N is continually "topped up".
Birth of succeeding offspring will maintain N near K
artificial selection on agricultural species
Gecko lizard (Aristelliger) has "suction pad" feet:
lamellar scale counts increase with
age
Darwin's Finch (Geospiza fortis) adapts to drought:
larger birds survive (Fig. 14-06)
because of change in seed size
& hardness
(recall that size is heritable)
Developmental
canalization
limits extent of directional selection
Systems are controlled by multiple epistatic loci:
it is difficult to select on all loci simultaneously
Organisms have mechanical limits:
size cannot increase indefinitely
Johanssen's bean experiment
Skull volume versus birth
canal diameter in Homo
Phenotypes are not infinitely plastic:
[But: Eozostrodon lineage evolved
into whales & bats]
(2) Stabilizing
Selection (AKA truncation selection)
Fitness
function has a "peak"
Trait
variance reduced around (existing) optimal phenotype,
trait mean unaffected
Limits:
elimination of variant alleles
or, 'weeding out' of disadvantageous variants
homozygosity at multiple loci:
difficult iff variance due to recessive alleles (Lab
#1)
inbreeding depression: loss of 'health'
in inbred lines
Examples:
Lab
#1: Elimination of non-cryptic
pepper moths (Biston)
Dark variants are eliminated
rapidly in light environments
Light variants are reduced
(more slowly) in dark environments (why?)
[This may look like an example of directional selection: why isn't it?]
Cold
shock in house sparrows (Passer) (Bumpus 1898)
Animals that die are at extremes of distribution
Birthweight
in Homo (Karn & Penrose 1951)
Modal birthweight is optimum for survival
(3) Diversifying
Selection (two kinds)
There
is a lot of variation: does selection explain it?
(A) Balancing
Selection:
Fitness
function has more than one peak (multi-modal)
Trait
variance increases
polymorphic["strict
sense"]: variation maintained within populations
Ex.: cornsnakes, tomatoes,
bell
peppers, snails,
scallops
polytypic:
variation distributed among populations
Ex.: shell patterns in Cepaea
snails
fraction of dark / banded shells varies with substrate
Limits:
segregational
genetic load:
loss
of reproductive potential due to production of less fit homozygotes
In Lab #1, Exercise #2, about 1/3 of
population "dies" in malarial environment
Overdominance:
heterozygotes
have superior fitness at a locus
because different alleles are favoured in different environments
Examples:
sickle-cell
hemoglobin in Homo ('Contradictory' selection)
Leucine Aminopeptidase (LAP) & salinity
tolerance in Mytilus mussels
heterodimers:
multimeric enzymes with polypeptides from different alleles
often show wider substrate specificity, kinetic properties (Vmax
& KM)
myoglobin in diving mammals
Heterosis:
heterozygosity at multiple loci improves general fitness
Hybrid
vigour: crossbreeding of inbred lines
improves fitness in F1
Marginal
epistasis: high 'Hobs' is 'good for you'
Ex.:
correlation between phenotype & genotype: antler
points in Odocoileus deer
Ex.:
fluctuating
asymmetry:
Acionyx
cheetahs
are lopsided
Maintaining polymorphic phenotypic variation by selection
Alternative
phenotypes favored in different environments
crypsis:
Cepaea
land
snails match background (Fig.
13-06)
Batesian
mimicry:
'Tasty' mimics converge on 'distasteful'
models
Viceroy converge on Monarch (Papilio) butterflies
Mullerian
mimicry:
Distasteful models converge on each other,
different combinations evolve in different parts of range
Heliconius butterflies (Plate
7 in Futuyma 1997)
aposematic(warning)
colouration warns off predators (Mertensian mimicry]
Ex.: scarlet kingsnake (nonvenomous) mimics
coral snake (highly venomous) [black /
red / yellow pattern]
Frequency-dependant
selection:
Fitness value of phenotype varies with frequency
apostaticpredation:
thrush
predation on Cepaea
'search image' changes when prey type becomes rare
'rare
male' effect: females prefer "different" male
Male zebra finches with artificial crest get more copulations (Fig.
20-13)
Sexual
Selection (Darwin 1871):
'exaggerated' phenotypes are disadvantageous somatically
but are favoured in competition for mates
secondary sex characteristics:
Sexual dimorphism in mallards,
peafowl,
& lions
Antlers in Cervidae are used in male-male
combat
Tail displays in peacocks attract mates
'Runaway
sexual selection': the Madonna
/ Ozzy Osborne Effect
Females choose males on basis of some distinctive trait
Offspring have exaggerated trait (males) & preference for
trait (females)
=> selection reinforces trait & preference for trait simultaneously
New phenotype spreads rapidly in population
(B) Disruptive
selection
Fitness
function is a valley
Trait variance increases (like balancing), BUT polymorphism is unstable
[Try NatSel with: q = 0.5, N = 9999, W0 = 1.0, W1 = 0.7, W2 = 1.0]
Polymorphism
can usually be maintained only temporarily:
One of the phenotypes will outcompete the other
unless
different phenotypes choose different niches (Ludwig Effect)
[and then this becomes Balancing Selection]
Scutellar
bristles in Drosophila(Thoday & Gibson 1962)
Selection for 'high #' versus
'low #' lines
=> 'pseudo-populations' with
reduced interfertility
Might disruptive selection contribute to speciation?
Natural selection is ordinarily defined
as
differential survival
& reproduction of individuals:
Can selection
operate on other biological units?
Can such
selection 'oppose' individual selection?
Genic (Gametic)
Selection
Differential survival & 'reproduction' of alleles
Meiotic
Drive:
t-alleles in Mus
ttis
sterile (W = 0)
Ttis
'tail-less' (cf. Manx cats) (W
< 1)
t alleles are preferentially segregated into gametes (80~90%)
=> f(t) is high in natural populations (40~70%)
even though it is deleterious to individuals
Kin (Interdemic)
Selection
Differential survival & reproduction of related (kin) groups
(families)
Related
individuals share alleles:r = coefficient
of relationship [see
derivation]
offspring & parents are related by r = 0.50 [They
share half their alleles]
full-sibs
"
"
r = 0.50
half-sibs
"
"
r = 0.25
first-cousins
"
"
r = 0.125
Inclusive
fitness (Wi)
of phenotype for individual i
= direct fitness of i + indirect fitness of relatives
j,k,l,...
Wi
= ai +
(rij)(bij)
summed over all relatives j,k,l,...
where: ai = fitness of i due
to own phenotype
bij = fitness of j due to i's phenotype
rij = coefficient of relationship
of i & j
If i & j are unrelated
warn: Windividual
= 0.0 + (0.0)(1.0) = 0.0
don't warn: Windividual = 1.0 + (0.0)(0.0) = 1.0
=> Such behaviors should not evolve among unrelated individuals
What is the fitness value in a kin group?
Wbrothers = 0.0 + [(0.5)(1.0)
+ (0.5)(1.0)] = 1.0
Wcousins = 0.0 + [8][(0.125)(1.0)]
= 1.0
J.B.S.
Haldane (1892-1964):
"I would lay down my life for two brothers
or eight cousins."
Parentingbehaviour:
'Broken wing' display in mother birds
Mother sacrifices herself for (at
least two) offspring
Altruisticbehaviour
(
"unselfish concern for others")
'Alarm calls' in Belding ground squirrels
(Spermophilus)
females warn more in related groups
Can behaviours to help unrelated individuals evolve?
Eusocial
insects
(Hymenoptera, Isoptera)
Haplodiploidy: females diploid, male
drones haploid
Females workers are sterile (Wi = 0): what is the selective
advantage?
related to queen or offspring by 1/2
related to sisters by 3/4
=> Care for sisters, don't have offspring
Natural Selection may be the most misunderstood
concept in biology.
It is ...
(1) Not "Survival
of the Fittest"
Herbert
Spencer (1820 - 1903) "Social Darwinism"
the
"naturalistic fallacy": 'is'
= 'ought'
[Darwinian theory was accepted in part because
it could be read to support British imperial ambition]
not
phenotype-specific mortality
notpredation(nor
inter-species
competition,
usually)
not
"Nature red in tooth
and claw"
Darwin:
plants in desert 'struggle' for water
not
equivalent to population growth:
population declined in semelparous example
(2) Not equivalent to evolution
Natural
Selection may conserve existing types (stabilizing selection).
Evolutionary
change ultimately requires new variation (mutation).
Migration,
population structure, genetic drift are important.
(3) Not a tautology (a self-evident statement; a circular argument)
"Why
do they survive? Cuz they're fit.
How do you know they're fit? Cuz they survive..."etc.
More like
a syllogism (an if / then statement;
a logical consequence):
(
2 &
W
& h2) =>
q
[cf. physics: F = M A depending on how Force,
Mass, & Acceleration are defined
arithmetic: 1 + 2 = 3 because I and II make III]
(4) Not "Mother Nature"
not
a force, not a thing that acts
[We don't say, "Arithmetic causes one plus two to equal three."
We might say, "One plus two equals three. That's arithmetic.]
not
good or bad (amoral)
no noun
/ verb / object distinctions
[In most languages, "nouns verb objects"
i.e., objects perform actions on other objects. Not.]
(5) Not teleological (goal-directed):
Evolution
does not have "goal", "direction", or "purpose"
(Homo sapiens are not the endpoint of evolution!)
Avoid
such phrases as "Natural Selection acts ..."
"in
order to ...",
"for the purpose of ...",
"so that ...",
"because its trying to ..."
Text material © 2005 by Steven M. Carr