The Long-tailed Widowbird (Euplectes progne), also known as the “Sakabula,” is a species of bird in the Ploceidae family. The species are found in sub-Saharan Africa.
The long-tailed widowbird is a medium-sized bird and one of the most common in the territories it inhabits. Adult breeding males are almost entirely black with orange and white shoulders (epaulets), long, wide tails, and a bluish white bill. Females are rather inconspicuous, their feathers streaked tawny and black with pale patches on the chest, breast and back, narrow tail feathers, and horn-color bills.
When flying, male long-tailed widowbirds are readily visible due to their extremely long tails. Between six and eight of their twelve tail feathers are approximately half a metre (approximately 20 inches) long. The tail during flight display is expanded vertically into a deep, long keel below the male as he flies with slow wingbeats 20 to 78 inches above his territory.
Because of the seemingly large cost to such male ornaments, the long-tailed widowbird has been the subject of extensive research into the function and evolution of sexually selected traits. This research has demonstrated the existence of female choice in sexual selection and indicates the trade-offs between sexual appeal and physical constraints with regard to the evolution of sexual ornaments.
The long-tailed widowbird was first described by Pieter Boddaert, a Dutch physician and naturalist, in 1783. The long-tailed widowbird is a member of the genus Euplectes, and therefore closely related to other species of widowbirds and bishops. The long-tailed widowbird is classified as a passerine bird in the weaver family, Ploceidae, named in 1758 by Carl Linnaeus in 1758. The long-tailed widowbird has several of the common morphological traits and dietary preferences of this family, including its rounded conical bill and feeding on seeds.
The males fly with their tails drooping and somewhat spread, and with slow regular movements of their wings. In wet weather, they are unable to fly due to their elongated tails. During the non-breeding season, long-tailed widowbirds congregate into flocks, which can be found roosting in reed beds.
Long-tailed widowbirds exhibit distinct sexual dimorphism. Males and females exhibit differences in behavior and morphological traits. Adult males are entirely black, including under their wing-covets. Males’ wing shoulders are orange red and their wing-covets white. Their bills are bluish white. Males are known for their distinctly long tails, which contain twelve tail feathers. Of these twelve tail feathers, between six and eight are approximately half a metre (approximately 20 inches) long. Males have wingspans of approximately 5 to 5.8 inches.
Females have a rather subdued coloration. The upper portion of the female’s body is streaked with buff or tawny and black. Female chests, breasts and flanks are slightly paler than their above coloring. The area under the wing-covets is black and the females’ tail feathers are narrow and pointed. Finally, their bills are horn-colored.
Charles Darwin first expressed his ideas on sexual selection and mate choice in his book The Descent of Man, and Selection in Relation to Sex in 1871 in response to questions surrounding the elaborate ornamentation that males of some species exhibit despite detrimental costs to survival and seemingly negative consequences for reproductive success. He proposed two explanations for such traits’ existences: these traits are useful in male-male combat or are preferred by females.
Relative to the first of Darwin’s theories on sexual selection, the process of female choice, though theoretically plausible, took a considerable amount of time to gain acceptance because Darwin had little, if any, firm evidence that females did in fact choose mate based on characteristics they found attractive. It took ninety years after Darwin’s initial proposal for the theory to be tested in what has become a classic example of Behavioral Ecology research.
The male long-tailed widowbird has one of the most remarkable ornaments among passerine birds. Their tails, which are often more than 20 inches long, are the most extreme sexual ornament among Euplectes and seem to in fact be detrimental to the survival of the male. Thus, the tail appears to oppose forces of natural selection in the basic sense by decreasing survival in individuals who carry the trait. It was for this reason that researchers have chosen to focus their research into female choice on the confusing example of the long-tailed widowbird.
Malte Andersson and colleagues tested Darwin’s (and Fisher’s) theory of female preference for ornamentation as the cause of extreme elongation of the male long-tailed widowbird’s tail. They changed the length of males’ tails and studied their relative mating success. Early in the breeding season, the territories of thirty-six males were mapped and the numbers of nests were counted. The experimenters used each male as his own control by subtracting the number of nests in each male’s territory before treatment from the total of nests after treatment. This reduced the influence of initial variation among male territories on the outcome of the experiment. In a randomized block experiment, the color-ringed males were partitioned among nine groups of four males each. These groups were similar in territory quality and tail length. The tail of one randomly selected male within each group was cut to about 5 inches in length. Each removed feather was then glued to the corresponding feather of another male, elongating his tail by 8 to 12 inches. The two other males in the group served as controls. One had his tail cut and repaired using glue, while the other’s tail was left unchanged.
A clear pattern of success emerged, with males with the elongated tails being the most successful, followed by the control (normal tail length) males, followed by the males with shortened tails. The result indicated that the long tail is favored by sexual selection through female choice of mates. Female preference for long tails is also seen in the Red-collared Widowbird.
The Andersson experiment demonstrated that female long-tailed widowbirds prefer supernormal tails, as males with elongated tails were found to be the most reproductively successful. Amazingly, the tail females found most attractive were longer than those that occur in the natural setting. This outcome was shown to be the result of female choice rather than differences in male behavior resulting from shortened tails: males with shortened tails neither became less active in courtship display, nor did they give up their breeding territories. Thus, the tail is used to attract females rather than in direct contests among males, which is further supported by the fact that males do not expand their tails during flight displays during territorial contests.
As of this time, the exact function of epaulet in male long-tailed widowbirds is unknown. But, its use does resemble that of the red-Winged blackbird, being displayed during courtship and threat displays. Thus, the two most conspicuous ornaments of the male birds in the two species may be favored by different forms of sexual selection: the tail of the long-tailed widowbird by female choice and the brightly colored epaulets of the long-tailed widowbird and red-winged blackbird by male contest competition.
These photos were taken at the Lake Nakuru Nature Preserve.