lecture 20
life history strategies
sets of physiological and behavioral features that incorporate not only reproductive traits but also survivorship, length-of-life characteristics, preferred habitat type, and competitive ability
life history strategies have important implications for
how populations grow and for the reproductive success of populations and species
types of life history strategies
-iteroparity versus semelparity
-continuous versus seasonal iteroparity
-R and K selection
-grime's triangle
semelparity (common in insects and invertebrates)
a pattern when offspring are produced in a single reproductive event
other organisms reproduced in
successive years or breeding seasons
iteroparity (common in vertebrates and perennial plants such as tree)
a pattern of repeated reproduction at intervals throughout the life cycle
seasonal iteroparity
species such as birds, mammals, or temperate forest trees have distinct breeding seasons that lead to distinct groups of individuals all born at the same time
continuous iteroparity
for a few species, individuals reproduced repeatedly and at any time of the year (as well as some parasites, and some primates exhibit this strategy
semelparous mode will favor if
the environments is stable, a single act of organism, will devote all energy in making offspring and not maintaining its own body
iteroparos mode wil favor is
survival of juveniles is very poor and unpredictable, repeated/long reproductions will increase survival
K-selected species
stable populations adapted to exist at or near the carrying capacity, K, of the environment
r-selected species
high rate of per capita population growth, r, but poor competitive ability
according to McArthur and Wilson such strategies can be considered a
continuum
type I
most individuals die late inlife
type II
individuals die at a uniform rate
type III
most individuals die at a young age
ruderals
are adapted to take advantage of habitat disturbance (annual plants adapted to colonizing disturbed areas)
competitors
are adapted to live in highly competitive but benign [not harmful] environments (many tree species)
stress tolerators
are adapted to cope with extreme environmental conditions such as high soil salt or temperatures that exist in salt marshes and deserts (mangroves and cacti)
grime's triangle
plant life histories based on a model in which stress, disturbance, and competition are the important selective factors (based on data in grime 1979)
life history strategies are subject to
evolution
virginia opossums (Dipelphis virginiana) life only
20 months on average
Austad (1993) found that possums living on Sapelo Island (GA) where no predators are found, lived
25% longer than average
life history traits vary
widely among different species
life histoy traits involve trade-offs
limited amount of energy to invest in survival, maintainance, and reproduction
natural selection optimizes life history in light of trade-offs
-maximizes number of offspring surviving to maturity
-depends on likelihood of survival to different age classes
kirkwood (1979,2000) noted that
cells require repair and argued that narutal selection should favor levels of seld-repair that are good enough to keep an organism in sonund condition only for as long as it has a reasonable chance of reproducing
data from opossums support predictions from
life history theory (island possums appeared to age slowly than the mainland possums)
predation risk drives life history evolution in
guppies
reznick et al. (2006)
compared guppies in streams with numerous predators to those in streams with few predators. fouund effect on number of offspring, offspring weight, and mean size at sexual maturity
trnasplant experiments deomstrate
rapid evolution of life history traits
transplanted fish exhibited rapid life history evolution in the
expected directions
trade-offs arise when
allocation of resources to one life history trait reduces investment in another trait
investment in reproduction often comes at the
expense of growth or body maintenance
brown anolis (anolis sagrei) with their ovaries removed,
grew faster, bigger, and lived longer
females are more likely than males to provide parental care
-males have less investment
-males have uncertain paternity
-these roles reversed in some species
fishers principle
states that a 1:1 sex ration is an evolutionarily stable strategy, but not all individuals are able to mate at all times
operational sex ratio (OSR)
is the ratio of male to female individuals who are available for reproducing at any given time (sexual selection becomes an important agent when members of one sex compete with each other to mate)
degree of polyandry
mean number of mates per females
male gulf pipefish cafry fertilized eggs in pouches. because males make bigger investment in rearing offspring,
males choose to mate with only a few high-quality females, eggs from larger females are more likely to develop into viable offspring
organisms may regulate the number of offpring to maximize
-miscarriage
-cannibalism
organisms may also regulate the sex ration of offspring to
maximize fitness
blank and nolan (1983)
found youn female red-winged blackbirds produced more females, while order females produced more male
sand gobies cannibalize eggs
these adjustments increase the proportion of offspring surviving
frequency-dependent selection
-production of each sex favored when rare
-rare sex has more mating opportunities
fewer feamles
sex ratio stabilizes (natural selection will favor mutant females that produce more males)
any population that deviates from the 50:50 sex ratio will be
shifted back to it by natural selection
females may alter sex ratios of
offspring
hymenopterans
often exhibit haplodiploidy (haploid males, diploid females) so females can alter sex ratio of offspring by choosing whether or not to fertilize eggs with sperm (fig wasps produce fewer mles with larger clutches)
trivers-willard hypothesis
states that parents in good condition tend to bias their offspring sex ration toward the sex with a higher variation in reproductive values, whereas parents in bad condition favor the opposite sex
mothers alter sex ratio depending on conditions
-produce females when in poor condition; daughters will likely have some offspring even if in poor condition
-produce males when in good condition; males likely to benefit more from being large and will more readily attract mates
some species switch sex in
trivers-willard-predicted manner (start as females and breed as such when young and small, but switch to male when they are large)
sex ratio adjustment in seychelles warblers
-with high resources females favored
-up to three helping daughters beneficial
-with low resources males favored
-disperse away from poor habitat
strategies to maximize offspring produced over a lifetime can
differ for the sexes
among penduline tits (remiz pendulinus), mothers and fathers has interest conflict over who should provide care the longest
consequently, male-only care, female-only care and biparental desertion all occur
parental-offspring conflict
occurs when parents benefit from withholding parental care from some offspring and invest in other offspring
skylark chicks within a nest compete for
attention with loud begging calls and bright red mouths
triming the feather of this chicks makes them
appear black, influencing parental feeding rates (sibling competition in American coots)
offspring-offspring conflict (sibling rivalry)
occurs when sibling compete for parental care for parental care or limited resources (in some cases it can lead to siblicide/the killing of another sibling)
parent-of-origin effect
effect on the phenotype of an offspring caused by an allele inherited from a particular parent (ex. hinny: result of horse stallion + female donkey)
genomic imprinting
occurs when genes inherited from one or the other parent are silenced due to methylation (offspring express either maternal or paternal copy of gene, but not both)
methylation
the process by which methyl groups are added to certain nucleotides (associated with altered gene expression)
wilkins and haig (2003) suggest that
imprinting genes evolved through conlfict between parents which is resolved in their offspring
intralocus seuxal conlfict
is a conflict between the fitness effects of alleles of a given locus on mals and females
senescence
deterioration in the biological functions of an organisms as it ages (cells accumulate malformed protein, immune less effective, etc)
calorie restriction can
slow the aging process (genes involved in repair switched on under stress
may involve trade-offs (increase fitness of an allele while decrease fitness of another allele)
worm mutants that age more slowly have lower fitness
transcription factor DAF-16 controls the expression of a battery of genes, many of which have small effects on
lifespan (promoting either aging ot longetivity) in Caenorhabditis elegans
genes that promote ageing include
some that encode yolk proteins and insulin-like INS-7
actuarial and reproductive senescence
age-related declines in survival and reproduction respectively (the rule in free-ranging populations of vertebrates
hamilton (1966) proposed that
the decrease in the force of natural selection inevitably leads to actuarial senescence in any age-structured population, but does not adress reproductive senescence
the force or strength of natural selection, a measure of how strongly selection acts on survival and/or reproduction,
declines as a function of age
aging exists because
selection is weak and ineffective at maintaining survival, reproduction, and somatic repair at old age
mutation accumulation (MA)
aging evolves because selection cannot efficiently eliminate deleterious mutations that manifest themselves only late in life
antagonistic pleiotropy (AP)
aging evolves as a maladaptive byproduct of selection for increased fitness early inlife, with beneficial early-life effects being genetically coupled to deleterious late-life effects that cause aging
aging clearly shortens lifdespan, but lifespan is also shaped by
selection fo an increased number of lifetime reproductive events (balance with pros and cons)
mother hypothesis
risk of reproduction at older age selects for reduced fertility (investment in current offspring)
grnadmother hypothesis
loss of fertility associated with shift in investment to grandchildren
human females live
long-reproductive lives