Competition (biology)
Competition is an interaction between organisms or species in which both require one or more resources that are in limited supply. Competition lowers the fitness of both organisms involved since the presence of one of the organisms always reduces the amount of the resource available to the other.
In the study of community ecology, competition within and between members of a species is an important biological interaction. Competition is one of many interacting biotic and abiotic factors that affect community structure, species diversity, and population dynamics.
There are three major mechanisms of competition: interference, exploitation, and apparent competition. Interference and exploitation competition can be classed as "real" forms of competition, while apparent competition is not, as organisms do not share a resource, but instead share a predator. Competition among members of the same species is known as intraspecific competition, while competition between individuals of different species is known as interspecific competition.
According to the competitive exclusion principle, species less suited to compete for resources must either adapt or die out, although competitive exclusion is rarely found in natural ecosystems. According to evolutionary theory, competition within and between species for resources is important in natural selection. More recently, however, researchers have suggested that evolutionary biodiversity for vertebrates has been driven not by competition between organisms, but by these animals adapting to colonize empty livable space; this is termed the 'Room to Roam' hypothesis.
Interference competition
During interference competition, also called contest competition, organisms interact directly by fighting for scarce resources. For example, large aphids defend feeding sites on cottonwood leaves by ejecting smaller aphids from better sites. Male-male competition in red deer during rut is an example of interference competition that occurs within a species.Interference competition occurs directly between individuals via aggression when the individuals interfere with the foraging, survival, and reproduction of others, or by directly preventing their physical establishment in a portion of the habitat. An example of this can be seen between the ant Novomessor cockerelli and red harvester ants, where the former interferes with the ability of the latter to forage by plugging the entrances to their colonies with small rocks. Male bowerbirds, who create elaborate structures called bowers to attract potential mates, may reduce the fitness of their neighbors directly by stealing decorations from their structures.
In animals, interference competition is a strategy mainly adopted by larger and stronger organisms within a habitat. As such, populations with high interference competition have adult-driven generation cycles. At first, the growth of juveniles is stunted by larger adult competitors. However, once the juveniles reach adulthood, they experience a secondary growth cycle. Plants, on the other hand, primarily engage in interference competition with their neighbors through allelopathy, or the production of biochemicals.
Interference competition can be seen as a strategy that has a clear cost and benefit. In order to cope with strong interference competition, other organisms often either do the same or engage in exploitation competition. For example, depending on the season, larger ungulate red deer males are competitively dominant due to interference competition. However, does and fawns have dealt with this through temporal resource partitioning — foraging for food only when adult males are not present.
Exploitation competition
Exploitation competition, or scramble competition, occurs indirectly when organisms both use a common limiting resource or shared food item. Instead of fighting or exhibiting aggressive behavior in order to win resources, exploitative competition occurs when resource use by one organism depletes the total amount available for other organisms. These organisms might never interact directly but compete by responding to changes in resource levels. Very obvious examples of this phenomenon include a diurnal species and a nocturnal species that nevertheless share the same resources or a plant that competes with neighboring plants for light, nutrients, and space for root growth.This form of competition typically rewards those organisms who claim the resource first. As such, exploitation competition is often size-dependent and smaller organisms are favored since smaller organisms typically have higher foraging rates. Since smaller organisms have an advantage when exploitative competition is important in an ecosystem, this mechanism of competition might lead to a juvenile-driven generation cycle: individual juveniles succeed and grow fast, but once they mature they are outcompeted by smaller organisms.
In plants, exploitative competition can occur both above- and below ground. Aboveground, plants reduce the fitness of their neighbors by vying for sunlight plants consume nitrogen by absorbing it into their roots, making nitrogen unavailable to nearby plants. Plants that produce many roots typically reduce soil nitrogen to very low levels, eventually killing neighboring plants.
Exploitative competition has also been shown to occur both within species and between different species. Furthermore, many competitive interactions between organisms are some combination of exploitative and interference competition, meaning the two mechanisms are far from mutually exclusive. For example, a recent 2019 study found that the native thrip species Frankliniella intonsa was competitively dominant over an invasive thrip species Frankliniella occidentalis because it not only exhibited greater time feeding but also greater time guarding its resources. Plants may also exhibit both forms of competition, not only scrambling for space for root growth but also directly inhibiting other plants' development through allelopathy.
Apparent competition
Apparent competition occurs when two otherwise unrelated prey species indirectly compete for survival through a shared predator. This form of competition typically manifests in new equilibrium abundances of each prey species. For example, suppose there are two species, which are preyed upon by food-limited predator species C. Scientists observe an increase in the abundance of species A and a decline in the abundance of species B. In an apparent competition model, this relationship is found to be mediated through predator C; a population explosion of species A increases the abundance of predator species C due to a greater total food source. Since there are now more predators, species A and B would be hunted at higher rates than before. Thus, the success of species A was to the detriment of species B — not because they competed for resources, but because their increased numbers had indirect effects on the predator population.This one-predator/two-prey model has been explored by ecologists as early as 1925, but the term "apparent competition" was first coined by University of Florida ecologist Robert D. Holt in 1977. Holt found that field ecologists at the time were erroneously attributing negative interactions among prey species to niche partitioning and competitive exclusion, ignoring the role of food-limited predators.