Natural selection is the central engine of evolution, driving adaptation and speciation across the tree of life. This module explores the profound mechanisms by which environmental pressures sift through biological variation, ultimately shaping the genetic makeup of populations over countless generations.
Variation is a fundamental prerequisite for natural selection. Without phenotypic and genotypic differences among individuals within a population, there can be no differential survival and reproduction. This variation arises from several key sources:
Biological organisms possess a remarkable capacity for exponential population growth. Species tend to produce far more offspring than the environment can sustainably support. Thomas Malthus originally posited this concept, noting that populations grow geometrically while resources grow arithmetically, leading inevitably to competition.
The "struggle for existence" emerges directly from overproduction and limited resources. In this struggle, individuals with heritable traits better suited to the local environment—adaptations—are more likely to survive and successfully reproduce, passing their advantageous traits to the next generation.
Natural selection can alter phenotypic distributions in a population in three primary ways:
One extreme phenotype is favored over all others. The allele frequency shifts steadily in one direction. This typically occurs in changing environments. E.g., the peppered moth (Biston betularia) during the industrial revolution.
Intermediate phenotypes are favored; both extremes are selected against. This reduces variance and maintains the status quo in stable environments. E.g., human birth weights—extremely small infants lose heat rapidly and succumb to infections, while excessively large infants face complications during childbirth.
Both extreme phenotypes are favored at the expense of intermediate forms. This bimodal trait distribution can eventually lead to sympatric speciation. E.g., seedcracker finches where large beaks crack hard seeds and small beaks handle soft seeds, but intermediate beaks are inefficient for both resources.
The Hardy-Weinberg equation models the relationship between allele and genotype frequencies in a non-evolving, mathematically idealized population.
Key Formulae:
$$ p + q = 1 $$
$$ p^2 + 2pq + q^2 = 1 $$
Where $p$ and $q$ represent the frequencies of the dominant and recessive alleles, respectively. H-W equilibrium operates under strict assumptions: no mutations, random mating, no gene flow, an infinitely large population size, and no natural selection.
Answer: Meiosis generates genetic variation through two primary mechanisms: crossing over during Prophase I, where homologous chromosomes exchange genetic material, and independent assortment during Metaphase I, where homologous pairs align randomly at the equator, creating unique combinations of maternal and paternal chromosomes in the resulting gametes.
Answer: Directional selection favors one extreme of a trait distribution, shifting the population average over time (e.g., increasing beak size in Galápagos finches during a prolonged drought). Stabilizing selection favors the intermediate phenotype, narrowing the trait distribution (e.g., human birth weights, where extremes face higher mortality risks).
Answer: First, find $q^2$: $q^2 = 1/2500 = 0.0004$. Thus, $q = \sqrt{0.0004} = 0.02$. Since $p + q = 1$, $p = 0.98$. The carrier frequency is $2pq = 2 \times 0.98 \times 0.02 = 0.0392$, meaning roughly 3.92% of the population are carriers.