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Historically, bird song complexity was thought to evolve primarily through sexual selection on males; yet, in many species, both sexes sing and selection pressure on both sexes may be broader. Previous research suggests competition for mates and resources during short, synchronous breeding seasons leads to more elaborate male songs at high, temperate latitudes. Furthermore, we expect male–female song structure and elaboration to be more similar at lower, tropical latitudes, where longer breeding seasons and year-round territoriality yield similar social selection pressures in both sexes. However, studies seldom take both types of selective pressures and sexes into account. We examined song in both sexes in 15 populations of nine-fairy-wren species (Maluridae), a Southern Hemisphere clade with female song. We compared song elaboration (in both sexes) and sexual song dimorphism to latitude and life-history variables tied to sexual and social selection pressures and sex roles. Our results suggest that song elaboration evolved in part due to sexual competition in males: male songs were longer than female songs in populations with low male survival and less male provisioning. Also, female songs evolved independently of male songs: female songs were slower paced than male songs, although only in less synchronously breeding populations. We also found male and female songs were more similar when parental care was more equal and when male survival was high, which provides strong evidence that sex role similarity correlates with male–female song similarity. Contrary to Northern Hemisphere latitudinal patterns, male and female songs were more similar at higher, temperate latitudes. These results suggest that selection on song can be sex specific, with male song elaboration favored in contexts with stronger sexual selection. At the same time, selection pressures associated with sex role similarity appear to favor sex role similarity in song structure.

We know little of the proximate mechanisms underlying the expression of signaling traits in female vertebrates. Across males, the expression of sexual and competitive traits, including ornamentation and aggressive behavior, is often mediated by testosterone. In the white-shouldered fairywren (Malurus alboscapulatus) of New Guinea, females of different subspecies differ in the presence or absence of white shoulder patches and melanic plumage, whereas males are uniformly ornamented. Previous work has shown that ornamented females circulate more testosterone and exhibit more territorial aggression than do unornamented females. We investigated the degree to which testosterone regulates the expression of ornamental plumage and territorial behavior by implanting free-living unorna merited females with testosterone. Every testosterone-treated female produced a male-like cloacal protuberance, and 15 of 20 replaced experimentally plucked brown with white shoulder patch feathers but did not typically produce melanic plumage characteristic of ornamented females. Testosterone treatment did not elevate territorial behavior prior to the production of the plumage ornament or during the active life of the implant. However, females with experimentally induced ornamentation, but exhausted implants, increased the vocal components of territory defense relative to the pretreatment period and also to testosterone-implanted females that did not produce ornamentation. Our results suggest that testosterone induces partial acquisition of the ornamental female plumage phenotype and that ornament expression, rather than testosterone alone, results in elevations of some territorial behaviors.

The White-shouldered Fairywren (Malurus alboscapulatus) is a tropical passerine bird distributed across much of New Guinea. White-shouldered Fairywrens are among few species of fairywren with exclusively tropical distributions and differ from better studied congeners in Australia because subspecies vary by female, but not male, coloration and morphology. As with many bird species in New Guinea, basic demographic, social, morphological, and breeding data are limited. From 2011 to 2018 we documented the basic biology of two subspecies representing extremes of the female ornamentation spectrum. Both subspecies form groups having an even operational sex ratio and appear to breed year-round. Extra-pair paternity occurs in the subspecies with female ornamentation; comparable data are lacking for the subspecies having unornamented females, but the greater scaled cloacal protuberance volume of males suggests similar or higher extra-pair paternity rates. Females of the ornamented subspecies are generally larger than those lacking ornamentation, but exhibit reduced tail lengths, which is thought to serve as a signal of social dominance in other fairywrens. After first achieving adult-like plumage, males and ornamented females retain ornamented plumage year-round; however, only males in the subspecies with unornamented females appear to exhibit delayed plumage maturation. Our discussion highlights similarities and differences between White-shouldered Fairywren life histories and those of better studied Australian Malurus species; we focus on tropical vs. temperate environments and variable female ornamentation, and we identify priorities for future research.