Sexual selection models describe the evolutionary processes
and mechanisms that shape the mating behaviour, mate choice, and reproductive
success of individuals within a population. Several prevailing sexual selection
models have been proposed to explain the diversity of mating strategies and
traits observed in nature.
Bateman's Principle:
Proposed
by: Angus Bateman
Description:
Bateman's principle suggests that the variance in reproductive success is
typically higher in males than in females due to differences in the investment
of gametes and parental care between sexes.
Example:
In many species of insects, such as fruit flies (Drosophila spp.), males typically
invest less in parental care and can mate with multiple females, leading to
greater variance in male reproductive success compared to females.
Parental Investment Theory:
Proposed
by: Robert Trivers
Description:
Parental investment theory posits that the sex that invests more in offspring
(usually females) will be more selective in choosing mates, while the other sex
(usually males) will compete for access to mates.
Example:
In birds, female peafowl (peahens) invest significantly in the production and
care of eggs and offspring, leading to strong mate choice and selection for
elaborate male peacock displays, which serve as indicators of genetic quality
and parental investment.
Runaway Selection:
Proposed
by: Ronald Fisher
Description:
Runaway selection occurs when a preference for a particular trait (e.g.,
exaggerated male ornaments) becomes genetically linked with the trait itself,
leading to the rapid evolution of elaborate traits through positive feedback.
Example:
The long tail feathers of male widowbirds (Euplectes
spp.) are believed to have evolved through runaway sexual selection.
Females prefer males with longer tails, leading to the rapid evolution of
increasingly elongated tail feathers in males over successive generations.
Handicap Principle:
Proposed
by: Amotz Zahavi
Description:
The handicap principle suggests that elaborate secondary sexual traits serve as
honest indicators of genetic fitness because they are costly to produce or
maintain and therefore only high-quality individuals can afford them.
Example:
The antlers of male deer (e.g., red deer, Cervus
elaphus) are energetically costly to grow and maintain and are used in
aggressive displays during mating season. Antler size and complexity serve as
honest indicators of male genetic quality and dominance.
Sensory Bias:
Proposed by: Ryan & Rand
Description:
Sensory bias occurs when a pre-existing sensory bias in females (or males)
predisposes them to prefer certain traits or behaviors, leading to the
evolution of exaggerated traits in the opposite sex.
Example:
Female guppies (Poecilia reticulata)
exhibit a preference for males with brightly colored spots, which resemble the
coloration of their preferred food sources. This preference has led to the
evolution of elaborate male coloration through sensory bias.
These
are just a few examples of prevailing sexual selection models in nature, each
offering insights into the evolutionary processes underlying mating behavior,
mate choice, and the evolution of secondary sexual traits across diverse
species.
0 Comments