scholarly journals Male size predicts extrapair paternity in a socially monogamous bird with extreme sexual size dimorphism

2014 ◽  
Vol 26 (1) ◽  
pp. 200-206 ◽  
Author(s):  
Sarah J. Wells ◽  
Weihong Ji ◽  
James Dale ◽  
Beatrix Jones ◽  
Dianne Gleeson
The Auk ◽  
1981 ◽  
Vol 98 (3) ◽  
pp. 457-465 ◽  
Author(s):  
William A. Searcy ◽  
Ken Yasukawa

Abstract In a between-species comparison of icterids, male survival decreases relative to female survival as the degree of sexual size dimorphism increases. This result is consistent with the hypothesis that male size is limited by survival selection in icterids; the degree of size dimorphism is known to correlate with the degree of polygyny in icterids, however, so the decreased relative survival of males in dimorphic species may be caused by some correlate of polygyny other than large size. Survival estimates based on records of recovery of dead birds show positive correlations between male size and male survival and between female size and female survival, but survival estimates based on recaptures of live birds fail to show such relationships.


1985 ◽  
Vol 63 (9) ◽  
pp. 2187-2193 ◽  
Author(s):  
Kevin M. O'Neill

Female digger wasps invest substantially in each of their offspring, laying relatively few, large eggs and providing the young with the insect prey on which they depend for food. In a study of six species in the genera Philanthus, Bembecinus, and Bembix, it was found that within each species, there is a positive correlation between female body size and both the size of their ovarial eggs and the size of the prey they provision. In five of the six species, females were larger than males on average. It is suggested that the apparent association between body size and certain aspects of parental investment by females may provide the directional selection pressure that results in the evolution of sexual size dimorphism in digger wasps. In one species, males and females have the same mean size, probably because, in this species, selection pressure on male size is similar to that on females.


2006 ◽  
Vol 84 (11) ◽  
pp. 1678-1682 ◽  
Author(s):  
B.H. King ◽  
M.E. Napoleon

How body size affects fitness of males relative to females is relevant to understanding the evolution of sexual size dimorphism and maternal sex-ratio manipulation. In most parasitoid wasps, mothers oviposit a greater proportion of daughters in larger hosts. The host-quality model describes how this may be adaptive. A major assumption of the model is that host size has a greater effect on the fitness of daughters than of sons. The assumption has often been tested indirectly by examining the effects of parasitoid size on fitness, because a parasitoid’s size generally increases with the size of the host on which it develops. The validity of this indirect method is examined here for the parasitoid wasp Spalangia endius Walker, 1839 parasitizing Musca domestica L., 1758. If the method is valid, effects of parasitoid size on fitness should match the effects of host size on fitness that were shown in a previous study. The effects matched in that both parasitoid size and host size affected the fitness of females but not of males. However, the aspects of female fitness that were affected differed. That female size but not male size affected fitness was consistent with the female-biased sexual size dimorphism of S. endius.


Evolution ◽  
2016 ◽  
Vol 70 (6) ◽  
pp. 1189-1199 ◽  
Author(s):  
Patrick T. Rohner ◽  
Wolf U. Blanckenhorn ◽  
Nalini Puniamoorthy

PeerJ ◽  
2017 ◽  
Vol 5 ◽  
pp. e3617 ◽  
Author(s):  
Carmen Fernández-Montraveta ◽  
Jesús Marugán-Lobón

Common scientific wisdom assumes that spider sexual dimorphism (SD) mostly results from sexual selection operating on males. However, testing predictions from this hypothesis, particularly male size hyperallometry, has been restricted by methodological constraints. Here, using geometric morphometrics (GMM) we studied for the first time sex-differential shape allometry in a spider (Donacosa merlini, Araneae: Lycosidae) known to exhibit the reverse pattern (i.e., male-biased) of spider sexual size dimorphism. GMM reveals previously undetected sex-differential shape allometry and sex-related shape differences that are size independent (i.e., associated to the y-intercept, and not to size scaling). Sexual shape dimorphism affects both the relative carapace-to-opisthosoma size and the carapace geometry, arguably resulting from sex differences in both reproductive roles (female egg load and male competition) and life styles (wandering males and burrowing females). Our results demonstrate that body portions may vary modularly in response to different selection pressures, giving rise to sex differences in shape, which reconciles previously considered mutually exclusive interpretations about the origins of spider SD.


2009 ◽  
Vol 123 (2) ◽  
pp. 165
Author(s):  
Sarah M. Ludlow

Sexual size dimorphism is common among birds, with males generally being larger than females. Sexual size dimorphism is typically more extreme in polygynous species; socially monogamous males are typically only 5% larger than females. However, cryptic sexual size dimorphism has been found in some socially monogamous species. I used standard external measurements as well as two internal measurements (keel length and pectoral muscle mass) to determine whether, or to what extent, Bohemian Waxwings (Bombycilla garrulus) exhibit sexual size dimorphism. Males were only slightly larger than females in all of the characters measured except keel and tarsus length. Keel and tarsus length were 0.6% and 1% longer, respectively, in females than in males. The similar size exhibited by males and females may be related to the amount of parental care provided by males. Smaller body size in males may reflect a trade-off between selection for increased male size and energetic constraints imposed by parental care.


Oikos ◽  
1991 ◽  
Vol 61 (3) ◽  
pp. 337 ◽  
Author(s):  
Harri Hakkarainen ◽  
Erkki Korpimäki ◽  
Erkki Korpimaki

The Auk ◽  
2007 ◽  
Vol 124 (2) ◽  
pp. 515-525 ◽  
Author(s):  
Michael T. Murphy

AbstractAmong socially monogamous birds, standard metrics suggest that males are only ∼5% larger than females. An untested assumption is that, with the exception of reproductive systems, males and females are scaled mirror images of one another. I used external morphological and skeletal data, and information on muscle mass and organ size, to test this assumption in a population of breeding Eastern Kingbirds (Tyrannus tyrannus). Male and female Eastern Kingbirds exhibited no differences in body mass or standard measures of size, except in a longer (∼6%) wing chord and tail in males. However, keel length, a character rarely measured in the field, was 9.7% larger in males. In principal component analysis, overall body size (PC1) failed to differ between the sexes unless keel length was included. Analysis of 16 skeletal characters also showed that only the bones associated with flight were larger in males. However, the most significant differences between the sexes was that lean dry pectoral muscle mass (LDPMM) was nearly 30% greater in males, whereas the alimentary tract was 27.5% heavier in females. Females also carried more fat. In both sexes, LDPMM scaled in a positive allometric manner with body mass (i.e., slope > 1.0), but the significantly higher slope of males suggested especially strong selection for large muscle mass and, presumably, greater power generation during flight. Eastern Kingbirds thus exhibit pronounced cryptic sexual size dimorphism, but it is not clear whether natural or sexual selection is responsible. These data call for a broader perspective for measuring and a re-evaluation of sexual size dimorphism in other socially monogamous species.Un Llamado de Atención: Dimorfismo Críptico en el Tamaño en un Paserino Socialmente Monógamo


2020 ◽  
Vol 287 (1918) ◽  
pp. 20192640 ◽  
Author(s):  
Curtis R. Horne ◽  
Andrew G. Hirst ◽  
David Atkinson

Variation in the degree of sexual size dimorphism (SSD) among taxa is generally considered to arise from differences in the relative intensity of male–male competition and fecundity selection. One might predict, therefore, that SSD will vary systematically with (1) the intensity of sexual selection for increased male size, and (2) the intensity of fecundity selection for increased female size. To test these two fundamental hypotheses, we conducted a phylogenetic comparative analysis of SSD in fish. Specifically, using records of body length at first sexual maturity from FishBase, we quantified variation in the magnitude and direction of SSD in more than 600 diverse freshwater and marine fish species, from sticklebacks to sharks. Although female-biased SSD was common, and thought to be driven primarily by fecundity selection, variation in SSD was not dependent on either the allometric scaling of reproductive energy output or fecundity in female fish. Instead, systematic patterns based on habitat and life-history characteristics associated with varying degrees of male–male competition and paternal care strongly suggest that adaptive variation in SSD is driven by the intensity of sexual selection for increased male size.


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