Role of fecundity selection on the evolution of sexual size dimorphism in mammals

2017 ◽  
Vol 128 ◽  
pp. 1-4 ◽  
Author(s):  
Marcelo H. Cassini
2020 ◽  
Vol 31 (3) ◽  
pp. 792-797
Author(s):  
Marcelo H Cassini

Abstract Sexual size dimorphism is biased toward males in most mammalian species. The most common explanation is precopulatory intramale sexual selection. Large males win fights and mate more frequently. In artiodactyls, previous tests of this hypothesis consisted of interspecific correlations of sexual dimorphism with group size as a surrogate for the intensity of sexual selection (Is). However, group size is not a proper measure of sexual selection for several reasons as is largely recognized in other mammalian taxa. I conducted an interspecific test on the role of sexual selection in the evolution of sexual dimorphism using the variance in genetic paternity as a proxy for the Is. I reviewed the literature and found 17 studies that allowed estimating Is= V/(W2), where V and W are the variance and mean number of offspring per male, respectively. A phylogenetic generalized least squares analysis indicated that dimorphism (Wm/Wf) showed a significant positive regression with the intensity of sexual selection but not group size (multiple r2= 0.40; F3,17= 12.78, P = 0.002). This result suggests that sexual selection may have played a role in the evolution of sexual size dimorphism in Artiodactyla. An alternative hypothesis based on natural selection is discussed.


2001 ◽  
Vol 133 (3) ◽  
pp. 311-313 ◽  
Author(s):  
P. Nosil

Sexual size dimorphism occurs in many species. Differences between males and females, in size or other characteristics, may result from sexual selection, fecundity selection, natural selection, non-adaptive processes, or a combination of these pressures (Darwin 1874; Selander 1966; Trivers 1976; Slatkin 1984; Shine 1989). In insects, females with large body size often produce more eggs than smaller females, and femalebiased sexual size dimorphism is commonly attributed to such fecundity selection (e.g., Preziosi and Fairbairn 1997; but see Leather 1988). Water boatmen are detrivorous or zoophagous aquatic insects often inhabiting small ponds of the Northern Hemisphere (Hungerford 1948; Nosil and Reimchen 2001). Female water boatmen are generally larger than males. In this note, I quantify the nature and magnitude of a previously undescribed sexual size dimorphism in a natural population of the water boatman Callicorixa vulnerata Uhler (Hemiptera: Corixidae). I tested for differences between males and females in mean trait size (body length, body weight, mid-leg tarsal length, mid-leg tarsal spine number), and also tested for sexual dimorphism in allometric relationships between tarsal traits and body length.


Oikos ◽  
2015 ◽  
Vol 125 (9) ◽  
pp. 1250-1260 ◽  
Author(s):  
Vicente García-Navas ◽  
Timothée Bonnet ◽  
Raúl Bonal ◽  
Erik Postma

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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