A lek is an aggregation of male animals gathered to engage in competitive displays, lekking, to entice visiting females which are surveying prospective partners for copulation. Leks are commonly formed before or during the breeding season. A lekking species is characterised by male displays, strong female mate choice, and the conferring of indirect benefits to males. Although most prevalent among birds such as black grouse, lekking is also found in insects including paper wasps, crustaceans, fishes, amphibians, reptiles and mammals.
A classical lek consists of male territories in visual and auditory range of each other. An exploded lek, as seen in the kakapo (the owl parrot), has more widely separated territories, but still in auditory range.
Lekking is associated with an apparent paradox: strong sexual selection by females for specific male traits ought to erode genetic diversity by Fisherian runaway, but diversity is maintained and runaway does not occur. Many attempts have been made to explain it away, but the paradox remains.
The term derives from the Swedish lek, a noun which typically denotes pleasurable and less rule-bound games and activities ("play", as by children). English use of lek dates to the 1860s. Llewelyn Lloyd's The Game birds and wild fowl of Sweden and Norway (1867) introduces it (capitalised and in single quotes, as 'Lek') explicitly as a Swedish term.
The term was originally used most commonly for black grouse (Swedish: "orrlek") and for capercaillie (Swedish: "tjäderlek"), and lekking behavior is quite common in birds of this type, such as sage grouse, prairie chicken, great bustard and sharp-tailed grouse. However, lekking is also found in birds of other families, such as the ruff, great snipe, Guianan cock-of-the-rock, musk ducks, hermit hummingbirds, manakins, birds-of-paradise, screaming pihas and the kakapo. Lekking is seen in some mammals such as fallow deer, Ugandan kob (a waterbuck), some pinnipeds, some bats, and the topi antelope. Lekking is found in amphibians such as moor frogs and bullfrogs, reptiles such as marine iguanas and some species of fish (e.g., Atlantic cod, desert pupfish, and the cichlid Astatotilapia burtoni). Even insects like the midge, ghost moth, and lesser wax moth demonstrate lekking behavior. Lekking is also found in some paper wasp species such as Polistes dominula, the orchid bee Eulaema meriana, in some butterfly species like the black swallowtail (Papilio polyxenes), and in tarantula hawks like Hemipepsis ustulata.
There are two types of lekking arrangements: classical and exploded. In the classic lekking system, male territories are in visual and auditory range of their neighbours. In an exploded lek, males are further away from one another than they would be in a classic lek. Males in an exploded lek are outside of visual range of one another, but they stay within earshot. Exploded lek territories are much more expansive than classic systems and are known to exhibit more variation. A well-known example of exploded leks is the "booming" call of the kakapo, the males of which position themselves many kilometres apart from one another to signal to potential mates.
Lek territories of different taxa are stable and do not vary in terms of size and location. Males often return to the same mating sites because of female fidelity. It has been shown that avian females such as the black grouse and great snipe are faithful to males and not mating sites. Successful males congregate in the same area as the previous breeding season because it is familiar to them, while females return to reunite with said males. Females do not return to a mating site if their male partner is not present. Another possible explanation for lek stability is from male hierarchies within a lek. In some species of manakins, subordinate betas may inherit an alpha's display site, increasing the chances of female visitation. Rank may also contribute to the stability of lek size, as lower ranking males may congregate to achieve a perceived optimal size as a way to attract females.
Some species of ants, such as red harvester ants, as well as certain bee species, like Tetragonisca angustula and Trigona spinipes exhibit lek-like mating patterns. Males form reproductive aggregations, congregating and collectively give off a pheromone that attracts reproductive females. The more males present to give off the pheromone, the stronger the attraction for the females.
Lek mating is relatively common among paper wasp species. For example, Polistes dominula males often fight with other males in mid-air to demonstrate their superiority and attractiveness. Males that lose fly away from the lek. Females fly through leks or perch near lekking areas to observe males before making choices on mates and they use the highly conspicuous abdominal spots on males, which are highly variable in size and shape, to aid in mate choice. Males with smaller, more elliptically shaped spots are more dominant over other males and preferred by females compared to males who have larger, more irregularly shaped spots. In comparison, Mischocyttarus flavitarsis males choose a perch site near female hibernation areas, rub their abdomens to mark their territory and wait 6–7 weeks for a female to approach. If an intruder approaches, the owner of the site lunges and grapples the other wasp. Typically, they fall off the perch site and finish the fight on the ground.
Costs and benefits
The main benefit for both sexes is mating success. For males, the costs stem from females’ preferences. The traits that are selected for may be energetically costly to maintain and may cause increased predation. For example, increased vocalization rate caused a decrease in the mass of male great snipes. Other costs can derive from male combat. For example, male great snipes regularly fight to display dominance or defend their territory, with females preferring victorious males. Aggressive male black grouse are preferred over non-aggressive males and when the males fight they tear feathers from each other's tails.
At first glance, it may seem that females receive no direct benefits from lekking, since the males are only contributing genes to the offspring in the absence of parental care or other benefits. However, lekking actually reduces the cost of female searching because the congregating of males makes mate selection easier. Females do not have to travel as far, since they are able to evaluate and compare multiple males within the same vicinity. This may also help reduce the amount of time a female may be vulnerable to predators. When under predatory pressure, female marbled reed frogs have been seen consistently to choose leks near their release sites, with high male calling rates reducing female search time.
Female mating preferences
A meta analysis of 27 species found that qualities such as lekking size, male display rate, and the rate of male aggression exhibit positive correlation with male success rates. A positive correlation was also found between attendance, magnitude of exaggerated traits, age, frequency of fights, and mating success. This female preference leads to mating skew, with some males being more successful at copulating with females. The variation in mating success is quite large in lek mating systems with 70-80 percent of matings being attributed to only 10%-20% of the males present.
The lek paradox
Since sexual selection by females for specific male trait values should erode genetic diversity, the maintenance of genetic variation in lekking species constitutes a paradox in evolutionary biology. Many attempts have been made to explain it away, but the paradox remains. There are two conditions in which the lek paradox arises. The first is that males contribute only genes and the second is that female preference does not affect fecundity. Female choice should lead to directional runaway selection, resulting in a greater prevalence for the selected traits. Stronger selection should lead to impaired survival, as it decreases genetic variance and ensures that more offspring have similar traits. However, lekking species do not exhibit runaway selection. In a lekking reproductive system, what male sexual characteristics can signal to females is limited, as the males provide no resources to females or parental care to their offspring. This implies that females gain indirect benefits from her choice in the form of "good genes" for her offspring. Amotz Zahavi argued that male sexual characteristics only convey useful information to the females if these traits confer a handicap on the male. The handicap principle may be a resolution to the lek paradox, for if females select for the condition of male ornaments, then their offspring have better fitness. One potential resolution to the lek paradox is Rowe and Houle's theory that sexually selected traits depend on physical condition, which might in turn, summarize many genetic loci. This is the genic capture hypothesis, which describes how a significant amount of the genome is involved in shaping the traits that are sexually selected. There are two assumptions in the genic capture hypothesis: the first is that sexually selected traits are dependent upon condition and the second is that general condition is attributable to high genetic variance. In addition, W. D. Hamilton and M. Zuk proposed that sexually selected traits might signal resistance to parasites. One resolution to the lek paradox involves female preferences and how preference alone does not cause a drastic enough directional selection to diminish the genetic variance in fitness. Another conclusion is that the preferred trait is not naturally selected for or against and the trait is maintained because it implies increased attractiveness to the male.
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There have been several hypotheses proposed as to why males cluster into leks. The hotshot hypothesis is the only model that attributes males as the driving force behind aggregation. The hotshot model hypothesizes that attractive males, known as hotshots, garner both female and male attention. Females go to the hotshots because they are attracted to these males. Other males form leks around these hotshots as a way to lure females away from the hotshot. A manipulative experiment using the little bustard, Tetrax tetrax, was done to test the various lek evolution models. The experiment involved varying the size and sex ratio of leks using decoys. To test whether or not the presence of a hotshot determined lek formation, a hotshot little bustard decoy was placed within a lek. After the fake hotshot was added to the lek, both male and female visitation to the lek increased.
The hotspot model considers the female density to be the catalyst for the clustering of males. This model predicts that leks will form where females tend to reside as a way to increase female interaction. Female manakin traffic has been observed to be concentrated around leks, bathing sites, and fruiting areas, with males aggregated near the most visited fruiting resources. The hotspot model also predicts that lek size is dependent upon the number of females inhabiting a patch of land. To test if the number of females affects lek formation, a group of female little bustard decoys were added to a lek. The presence of these female decoys did not have an effect on lek size.
The blackhole model proposes that females have a preference for neither size nor type of male, but rather that females tend to be mobile and mate wherever leks may be located. This model predicts that female mobility is a response to male harassment. This prediction is difficult to test, but there was a negative correlation found between male aggressiveness and female visitation in the little bustard population. Evidence supporting the black hole model is mainly found in ungulates.
An alternative hypothesis for lekking is kin selection, which assumes that males within a lek are related to one another. As females rarely mate outside of leks, it is advantageous for males to form leks. Although not all males within a lek mate with a female, the unmated males still receive fitness benefits. Kin selection explains that related males congregate to form leks, as a way to attract females and increase inclusive fitness. In some species, the males at the leks show a high degree of relatedness, but this does not apply as a rule to lek-forming species in general. In a few species such as peacocks and black grouse, leks are composed of brothers and half-brothers. The lower-ranking males gain some fitness benefit by passing their genes on through attracting mates for their brothers (larger leks attract more females). Peacocks recognize and will lek with their brothers, even if they have never met before.
Another hypothesis is predator protection, or the idea that there is a reduction in individual predation risk in a larger group. This could work both for the males in within the group as well as any female who visits the lek. Protection also explains the presence of mixed leks, when a male of one species joins a lek of another species for protection from a common set of predators. This occurs with manakins, as well as other birds such as grouse species.
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