The blue-tailed damselfly or common bluetail (Ischnura elegans) is a damselfly, belonging to the family Coenagrionidae.

Subspecies and varieties

Subspecies and varieties include:

  • Ischnura elegans ebneri Schmidt, 1938
  • Ischnura elegans elegans (Vander Linden, 1820)
  • Ischnura elegans pontica Schmidt, 1939
  • Ischnura elegans f. infuscans
  • Ischnura elegans f. infuscans-obsoleta
  • Ischnura elegans f. rufescens
  • Ischnura elegans f. typica
  • Ischnura elegans f. violacea

Distribution

This species is present in most of Europe and the Middle East. It is a common species.

Habitat

These damselflies can be found in a wide range of lowland environments, with standing and slow flowing waters, brackish and polluted water. Adult male blue-tailed damselflies have a head and thorax patterned with blue and black. There is a bi-coloured pterostigma on the front wings. Eyes are blue. At rest, the wings of most damselfly species are held back together, unlike dragonflies, which rest with their wings out flat. The thorax of juvenile males has a green tinge.

Female polymorphism

In damselfly populations, there is often a surplus of males displaying male mate harassment. In order to avoid unwanted mating attempts, females have developed polymorphisms that allow some of them to avoid recognition by males by mimicking male phenotypes. There are three specific morphs found in the Ischnura elegans species: androchromes, aurantiaca(rufescens) and infuscans. The androchromes resemble the male coloration, and the gynochromes, which can be either aurantiaca or infuscan, do not resemble males. The aurantiaca female morph is a pink-orange color with a blue abdominal patch that eventually disappears after maturation. The third morph, infuscan, displays an olive-green coloration with no color on its abdominal patch. Females are able to fully mature into their differing morph colorations just a few days after they finish their transition from aquatic larvae to their mature forms.

Although having an increased number of morphs makes it more difficult for males to distinguish between males from females, the levels of male mate harassment is different between the different morphs. Males primarily rely on visual cues to distinguish between the morphs and can also use odour cues, secondarily. Androchromes are often seen to face less male mate harassment because they resemble males and are less desired.  This gives androchromes an advantage in that they are able to spend more time allowing their eggs to mature instead of exerting energy avoiding unwanted mating attempts. Along with that, the morphs also display different mate avoidance tactics. Androchromes are more likely to face off with males by spreading their wings and curling their abdomens while gynochromes tend to fly away to avoid mating. Despite potentially having more time for egg maturation, the androchromes are still disadvantaged because their abdomens, like males, are more narrow which prevents them from being able to carry as many eggs as gynochromes.

There are also five main hypotheses that attempt to understand how the different female polymorphisms are continually maintained in this species. The reproductive isolation hypothesis states that there is a greater predation pressure on androchromes, which is seen as a trade-off to maintain the more inconspicuous morph. The male-mimicry hypothesis, mentioned previously, proposes that the androchromes ability to mimic male coloration allows them to avoid unwanted mating attempts and allocate more time to egg maturation. The density-dependent hypothesis states that the maintenance of the polymorphisms is attributed to the changing population densities. The habituation hypothesis states that males are actually most attracted to the morph that is most abundant.

Mating and behavior

This species participates in a male scramble mate choice mating system in which a male's mating success is determined by how fast they are able to find a mate. This includes many hours of copulations in which males are unable to monopolize a single female and some males are often left with no mates at all. Due to this, the I. elegans species displays intense male-male competition which leads to males forcing copulations with females. Along with the lengthy copulations, the reproductive lifespan of this species is only a few weeks. Cooperation from both males and females is required for copulation and females have the ability to reject sperm transfer from unwanted mating attempts. A tandem formation is created by males through the clasping of the female pronotum. In response to changing social contexts and population densities, males may change their sexual preferences and choose to mate with other males.

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File:Blue-tailed damselflies (Ischnura elegans) mating, female typica 2.jpg|Mating, female f. typica

File:Blue-tailed damselfly (Ischnura elegans) nymph.jpg|nymph

File:Ischnura elegans emerging.jpg|emerging

File:Blue-tailed damselfly (Ischnura elegans) immature male.jpg|Immature male

Blue-tailed damselfly (Ischnura elegans) teneral female rufescens.jpg|teneral female form rufescens

File:Blue-tailed damselfy (Ischnura elegans) female rufescens.jpg|Female form rufescens

File:Blue-tailed damselfly (Ischnura elegans) female violacea 2.jpg|Female form violacea

File: Blue-tailed damselfly (Ischnura elegans) female rufescens-obsoleta 2.jpg|Female form rufescens-obsoleta

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References