Size-Dependent Selective Mechanisms on Males and Females and the Evolution of Sexual Size Dimorphism in Frogs

2014 ◽  
Vol 184 (6) ◽  
pp. 727-740 ◽  
Author(s):  
Renato C. Nali ◽  
Kelly R. Zamudio ◽  
Célio F. B. Haddad ◽  
Cynthia P. A. Prado
Author(s):  
P. M. Parés- Casanova ◽  
A. Kabir

Sexual dimorphism, defined as phenotypic differences between males and females, is a common phenomenon in animals. In this line, Rensch’s rule states that sexual size dimorphism increases with increasing body size when the male is the larger sex and decreases with increasing average body size when the female is the larger sex. Domesticated animals offer excellent opportunities for testing predictions of functional explanations of Rensch’s theory. Pigeon breeds encounters many different functional purposes and selective constraints, which could influence strongly their morphology. The aim of this paper is to examine, for first time, Rensch’s rule among domestic pigeons. It was compiled a database of 12 quantitative traits (body weight, body height, beak thickness, beak length, neck length, neck thickness, wing length, rump width, tail length, tarsus length, tarsus thickness and middle toe length) for males and females of 11 different domestic pigeon breeds: Bangladesh Indigenous, Racing Homer, Turkish Tumbler, Indian Lotan, Kokah, Mookee, Indian Fantail, Bokhara Trumpeter, Bombai, Lahore and Hungarian Giant House; Rock Pigeon (Columba livia) was also considered as wild relative for comparative purposes. Comparative results between males and females showed that only body weight, wing length and neck thickness were consistent with Rensch’s rule. The rest of trait did not present correlations. Among domestic pigeons, there can appear different expressions of dimorphism according to each trait, so it must be considered that Rensch’s rule vary when considering other traits than body weight.


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.


2020 ◽  
Vol 131 (3) ◽  
pp. 600-610
Author(s):  
Nelson Rodrigues Silva ◽  
Bianca V M Berneck ◽  
Helio R da Silva ◽  
Célio F B Haddad ◽  
Kelly R Zamudio ◽  
...  

Abstract Female fecundity is an important selective force leading to female-biased sexual size dimorphism (SSD) in frogs. Because anurans exhibit diverse reproductive modes, we investigated whether variation in SSD and fecundity are related with oviposition site. We asked whether arboreal breeding species show pronounced female-biased SSD and if, paradoxically, females have lower fecundity because of the costs of carrying oocytes and amplectant males. Conversely, we tested whether species that deposit eggs in concealed sites show less pronounced SSD, because females do not carry males and space limitation may reduce female size and fecundity. Our results showed that, in general, males were approximately 20% smaller than females. However, for species with hidden oviposition sites, males and females exhibited more similar body sizes and arboreal hylids showed more pronounced female-biased SSD. Overall, fecundity was higher in aquatic breeders, as expected, but in hylids, fecundity was smaller in arboreal breeders, which suggests that arboreality may impose restrictions on fecundity. By analysing SSD in a broader and more specific lineage (Hylidae), we found that reproductive microhabitat may also influence female size and fecundity, playing an important role in the evolution of SSD in frogs at different evolutionary scales.


1994 ◽  
Vol 72 (9) ◽  
pp. 1543-1550 ◽  
Author(s):  
Nicola Saino ◽  
Fiorenza De Bernardi

Sexual size dimorphism was analysed across a hybrid zone existing between allopatric populations of Carrion Crows and Hooded Crows (Corvus corone corone and C. c. cornix) in northwestern Italy. Twenty-five morphological (osteological and plumage) variables were measured in a sample of 1599 specimens obtained from allopatric parental areas and from the hybrid zone. For each morphological variable considered, sexual size dimorphism was measured as the ratio of males/females or the absolute difference between mean sizes of males and females within each subpopulation studied. Overall sexual size dimorphism was described by discriminant function analysis. All the sexual size dimorphism measures adopted showed variation across the hybrid zone according to elevation. Male/female ratios and male–female differences significantly differed between the parental allopatric "operational taxonomic units," Carrion Crows being more dimorphic than Hooded Crows. Across the hybrid zone, sexual size dimorphism was correlated with the phenotypic composition of the crow subpopulations and with size of males but not size of females. The data presented show that sexual size dimorphism is correlated with an ecological gradient and that its geographical variation is determined by variation in size of males only.


2019 ◽  
Vol 97 (4) ◽  
pp. 304-311
Author(s):  
M.N. Rossi ◽  
E.B. Haga

Rensch’s rule states that males vary more in size than females when body size increases. The main cause of Rensch’s rule has been credited to sexual selection. However, different degrees of plasticity between the sexes have also been proven to be useful for describing variations in sexual size dimorphism, particularly within an intraspecific context. For insects, in general, this rule has rarely been tested within species. Here, we tested whether Acanthoscelides macrophthalmus (Schaeffer, 1907) (Coleoptera: Chrysomelidae: Bruchinae) followed Rensch’s rule when individuals emerged from seeds immediately after fruit collection and when they were reared for one generation, by measuring three morphological traits. Rensch’s rule was not followed for any of the morphological traits. Variations in body size were similar in males and females for bruchines that first emerged from seeds and for those that were reared for one generation. These findings suggest that environmental conditions (e.g., temperature, humidity, and seasonality) are unlikely to drive differential plasticity in males and females of this seed-feeding beetle. It is possible that changes in the body size of A. macrophthalmus have a genetic basis. However, regardless of whether variations in body size have a genetic basis, our findings provide no support for Rensch’s rule.


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.


2020 ◽  
pp. jeb.235697
Author(s):  
Michael L. Logan ◽  
Lauren K. Neel ◽  
Daniel J. Nicholson ◽  
Andrew J. Stokes ◽  
Christina L. Miller ◽  
...  

If fitness optima for a given trait differ between males and females in a population, sexual dimorphism may evolve. Sex-biased trait variation may affect patterns of habitat use, and if the microhabitats used by each sex have dissimilar microclimates, this can drive sex-specific selection on thermal physiology. Nevertheless, tests of differences between the sexes in thermal physiology are uncommon, and studies linking these differences to microhabitat use or behavior are even rarer. We examined microhabitat use and thermal physiology in two ectothermic congeners that are ecologically similar but differ in their degree of sexual size dimorphism. Brown anoles (Anolis sagrei) exhibit male-biased sexual size dimorphism and live in thermally heterogeneous habitats, whereas slender anoles (Anolis apletophallus) are sexually monomorphic in body size and live in thermally homogeneous habitats. We hypothesized that differences in habitat use between the sexes would drive sexual divergence in thermal physiology in brown anoles, but not slender anoles, because male and female brown anoles may be exposed to divergent microclimates. We found that male and female brown anoles, but not slender anoles, used perches with different thermal characteristics and were sexually dimorphic in thermal tolerance traits. However, field-active body temperatures and behavior in a laboratory thermal arena did not differ between females and males in either species. Our results suggest that sexual dimorphism in thermal physiology can arise from phenotypic plasticity or sex-specific selection on traits that are linked to thermal tolerance, rather than from direct effects of thermal environments experienced by males and females.


2014 ◽  
Vol 64 (1) ◽  
pp. 87-95 ◽  
Author(s):  
Di Lu ◽  
Cai Quan Zhou ◽  
Lian Jun Zhao ◽  
Wen Bo Liao

Rensch’s rule describes that sexual size dimorphism (SSD) increases with body size (hyperallometry) when males are larger, and decreases with body size (hypoallometry) when males are smaller. In this paper, on the basis of mean adult body size resulting from 18 populations of the common frogRana temporariaand 24 populations of the Tibetan frogNanorana parkeri, we tested the consistency of allometric relationships between males and females with Rensch’s rule. Our results show that the variation in degree of female-biased SSD increased with increasing mean size at intraspecific levels in two species, which is consistent with the inverse of Rensch’s rule. Furthermore, we tested the hypothesis that the degree of SSD decreased with increasing altitudes. Inconsistent with the predications of our hypothesis, we found no relationships between the degree of SSD and altitude for the two species investigated. These findings suggest that females living in adverse climates in high altitudes cannot adjust their body size as plastically as males.


2020 ◽  
Vol 13 (1) ◽  

Chitala ornata (J.E. Gray) (Osteoglossiformes: Notopteridae) has since established abundant and nuisance populations in Laguna de Bay. A fundamental prerequisite for the development of management strategies for invasive species like C. ornata is a full understanding of its life history characteristics including sexual dimorphism. In the present study, we examined the sexual dimorphism of C. ornata. Sexes of C. ornata can be distinguished through the examination of its genital papilla wherein females show distinct morphological adaptions for effective oviposition on a spawning substrate. Comparison of means and multivariate analysis of several morphometric characters showed that sexual size dimorphism in C. ornata is female-biased which is mainly attributed to the disparity of resource expenditure between sexes for reproduction and size-dependent advantages of females in the production of more progenies with better chances of survival.


Author(s):  
Chloe Boynton

Size differences between males and females (sexual size dimorphism) are often seen in a variety of species. In birds of prey in particular, a phenomenon occurs where the female is larger than the male. One of the main hypotheses attempting to explain sexual size dimorphism in birds of prey is that the female and male differ in size to partition resources, like prey. There is also evidence that predator and prey body size are correlated, so predators of similar size may be in direct competition. It has been shown that when two closely related species interact in the same area, they are likely to be in competition for similar resources, like prey. This study is looking at sexual size dimorphism and closely related species interactions, which has never been looked at before in birds of prey. I am using the subfamily Buteoninae (Buteo Hawks) as my focal group. I will be using sexual size dimorphism ratios, estimates of genetic distance between closely related species and proportion of range overlap between different closely related lineages within the subfamily. I am expecting to see that if species are closely related and inhabit the same area they will have a decreased sexual size dimorphism. This is because both species are likely to be competing for the same resources, and to avoid competition the species will diverge in body size from one another. This will cause the male and female of each species to converge in size, reducing their sexual size dimorphism.


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