According to classical sexual selection theory, complex multimodal courtship displays have evolved in males through female choice. While it is well-known that socially monogamous songbird males sing to attract females, we report here the first example of a multimodal dance display that is not a uniquely male trait in these birds. In the blue-capped cordon-bleu (Uraeginthus cyanocephalus), a socially monogamous songbird, both sexes perform courtship displays that are characterised by singing and simultaneous visual displays. By recording these displays with a high-speed video camera, we discovered that in addition to bobbing, their visual courtship display includes quite rapid step-dancing, which is assumed to produce vibrations and/or presumably non-vocal sounds. Dance performances did not differ between sexes but varied among individuals. Both male and female cordon-bleus intensified their dance performances when their mate was on the same perch. The multimodal (acoustic, visual, tactile) and multicomponent (vocal and non-vocal sounds) courtship display observed was a combination of several motor behaviours (singing, bobbing, stepping). The fact that both sexes of this socially monogamous songbird perform such a complex courtship display is a novel finding and suggests that the evolution of multimodal courtship display as an intersexual communication should be considered.

Birdsong is a sexual signal that serves as an indicator of male quality. There is already abundant evidence that song elaboration reflects early life-history because early developmental stress affects neural development of song control systems, and leaves irreversible adverse effects on song phenotypes.Especially in closed-ended vocal learners, song features crystallized early in life are less subject to changes in adulthood. This is why less attention has been paid to lifelong song changes in closed-ended learners. However, in the eyes of female birds that gain benefits from choosing mates based on male songs, not only past but also current conditions encoded in songs would be meaningful, given that even crystallized songs in closed-ended learners would not be identical in the long term. In this study, we examine within-individual song changes in the Java sparrow Lonchura oryzivora, with the aim of shedding light on the relationship between song and long-term life history. Specifically, we compared song length, tempo, and song complexity measures between the point just after song crystallization and around 1 year later, and also compared those traits between fathers and sons to clarify the effect of vocal learning. While it is not surprising that song complexity did not differ depending on age or between fathers and sons, we found that song length and tempo increased with age. Follow-up analyses have revealed that frequency bandwidth and peak frequency of song notes also elevated with age. Our results show that song performance related to motor skills can be improved even after song crystallization. We also suggest that song performance in closed-ended vocal learners gives a reliable clue for mate choice by reflecting male quality with aging.

Socially monogamous songbird couples show off their courtship display in front of other individuals.

A comparative study was conducted on the ontogenetic variation in morphometry of a total of 29 shellbearing molluscan species occurring on an intertidal stony shore in south-western Japan. The relationships between shell size and total weight and between shell size and¯esh weight were all highly signi®cant on logarithmic scales with the slopes having values of about three. The arcsine-transformed proportion of shell weight out of total weight varied among and within different morphological/taxonomic groups, ranging from 58.6% in Acanthochiton de®lippi to 76.4% in Nerita albicilla. The allometry of shell weight was analysed by regressing the arcsine transformed values of the proportion of shell weight against total weight in each species. The slope (b) of the regression varied substantially among different taxa, with all three possible cases, i.e. b > 0, b & 0 and b < 0, being observed. Thus, depending on molluscan species, the proportion of shell mass either (1) increases, (2) does not change, or (3) decreases with increasing body mass. Variation in the value of b was to some extent explained by the proportion of shell mass of young individuals of each species; species with relatively high proportions of shell mass in small individuals tended to have low b. Interspeci®cally, it was shown that shell mass scaled in proportion to body mass for this assemblage of 29 species. Consideration was given to the theoretical background of variation in shell morphometry, with particular reference to the shell as a defence structure.