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Lecture 2: Analysis of Adaptation • Adaptation = a feature that, because it increases fitness, has been shaped by NS • In other words: NS + genetic variation = adaptation • Adaptations are not always obvious e.g. Eyesight vs. Giraffe’s neck Adaptations When analyzing adaptation we need to remember: • Not all features of a population are adaptive • Not all adaptations are perfect Analysis of Adaptation We need to: • Show that a trait has been shaped by NS • Determine the agent of selection 4 Ways to Identify an Adaptation 1) COMPLEXITY • Complex structures are usually adaptive e.g. ampullae of Lorenzini • Variants of complex structures may not be adaptive (e.g. Hb) 2) Engineering Does the trait fit efficient model predicted by engineering? e.g. Fish shapes • Fits aerodynamic prediction • Form fits function 3) Convergence Correlational Evidence: Convergent Evolution • Patterns of convergence are studied using the COMPARATIVE METHOD • Variation in character should correlate with selective pressures of ecological context • Problem: similarity can mean similar adaptive response or close relationship • Need: traits that arise independently in different phylogenies • Eliminate the effect of common ancestry; therefore ecology is the determining factor • Thus need correct phylogeny = Biparental care = Nest parasitism Conclusion: biparental care = adaptive response Experiments 4) Experimental manipulation • Manipulate a trait and see if affects fitness • e.g. Swallow’s tails • e.g. Bower birds • e.g. Zonosemata flies Zonosemata • Dark banded wings, waving behaviour • Main predator: jumping spiders • Does wing colouration or waving reduce predation? (mimicry?) • 5 test flies: • Untreated Zonosemata, sham surgery, housefly wings, housefly with Zonosemata wings, housefly • Against jumping spider and other predator • Needed to have both markings & waving to repel jumping spider (no surgery effect) • No effect on any other predators • Mimic jumping spiders to avoid jumping spider predation Cepea nemoralis • Snails vary in colour & # of bands (polymorphism) • Morphotype varies with habitat • Why? – Engineering: thermoreg’n depends on darkness – Experimental: camouflage – thrush predation Examples 1. Evolution of sex 2. Sexual selection 3. Evolution of sex ratio Evolution of Sex • Sex is costly so why is it so common? • Asexual reproduction is only found in patches on the phylogenetic tree • Asexual species have higher rates of extinction than sexual species Model: Asexual variant • e.g. Given each female has 2 offspring, no difference in survival Asexual Sexual Frequency 100 females 100 females (100 males) p(female) = 0.33 200 females 100 females (100 males) p(female) = 0.5 400 females 100 females (100 males) p(female) = 0.67 Sexual vs. Asexual • Sexual females lose ½ genes in each generation – to survive to repro females must be fit but their mate may be less fit • Sexual female has ½ fitness of asexual • Plus, costs of finding a mate, STDs etc. • Given this disadvantage, there must be a benefit in sexual reproduction Model’s Assumptions Violated 1. Reproductive mode does not affect number of offspring Parental care/Nuptial gifts (fairly rare) 2. Reproductive mode does not affect survival of offspring Group Selectionist Argument: sex accelerates rate of evolution • Increases a group’s ability to respond to changing environment • Asexual populations have a higher extinction rate Given 2 loci with 2 alleles (Aa Bb): p(A) >>> p(a) p(B) >>> p(b) (A & B are “fixed”) a & b interact to increase fitness How get aabb in one individual? 1) Asexual: AABB aabb only by mutation get AaBB and AABb but: p(AABB aabb) 0 1) Sexual: recombination AaBB x AABb Gives: AABB; AaBB; AABb; AaBb AaBb x AaBb = aabb Mutant genotype can arise quickly and prevent extinction Mutation rate is important Mutation rate slow Sexual Asexual No advantage to sex Mutation rate fast Sexual > Asexual Thus, sexual pop’ns can outcompete asexual pop’ns Sex is still disadvantageous to the individual