Sexual dimorphism and evidence for intrasexual selection from quill impalements, injuries, and mate guarding in porcupines (Erethizon dorsatum)

1997 ◽  
Vol 75 (6) ◽  
pp. 847-854 ◽  
Author(s):  
Richard Alan Sweitzer ◽  
Joel Berger

Sexual selection is a commonly cited explanation for sexual size dimorphism. We examined patterns of sexual dimorphism in North American porcupines (Erethizon dorsatum) and used data on quill impalements, injuries, and guarding behavior to examine the intrasexual component of sexual selection among male porcupines. Results indicated that porcupines were sexually dimorphic for foot-pad length, body length, and body mass because males grew more rapidly and for longer periods than females. Quill impalements, injuries, and guarding episodes were restricted predominantly to older, larger males, intimating that only the largest porcupines were reproductively active. Regression analyses suggested that size was more important than age in predicting reproductive activity among males. Also, relatively few quill impalements and guarding episodes among younger, smaller animals suggest that there is a threshold size below which male porcupines do not attempt to compete for mate access. Although our data do not directly link larger body size in males with relatively high reproductive success, they suggest that sexual dimorphism in this species is at least partly the result of the intrasexual component of sexual selection. It is also possible that females select males on the basis of quill morphology or some other indicator of male quality. Thus, our understanding of sexual dimorphism in porcupines would benefit from additional research investigating the extent to which body size and patterns of quill number or size are advantageous to male porcupines in garnering mating opportunities and enhancing fitness.

1993 ◽  
Vol 71 (2) ◽  
pp. 346-351 ◽  
Author(s):  
Donald T. Stewart

The pattern of sexual dimorphism in thick-billed murres, Uria lomvia, from the Lancaster Sound – Jones Sound region, Northwest Territories, was examined for weight and 21 skeletal characters. Univariate statistics (Bonferroni-corrected t-tests) indicated that males were significantly larger than females in 6 bill and skull characters. Multivariate statistics also indicated that males had larger bills and skulls than females (based on canonical discriminant analysis), but males were not larger than females in overall body size (as defined by the first principal-components axis). The direction and magnitude of dimorphism were consistent with a hypothesis based on sexual selection as the driving force. In particular, large bill and skull sizes in males are consistent with agonistic behaviours associated with male–male competition for breeding sites and mate guarding.


2020 ◽  
Vol 40 (6) ◽  
pp. 649-656
Author(s):  
Juan C Azofeifa-Solano ◽  
Jeffrey A Sibaja-Cordero ◽  
Ingo S Wehrtmann

Abstract The sexual selection over traits that favor access to mating partners could promote the emergence of sexual dimorphism when the pressure is different between sexes. Monogamous species are considered to have a low degree of sexual dimorphism. The highly diverse snapping shrimps are usually regarded as monogamous, but the mating system has been studied only in few species. We aimed to provide insights into the mating system and sexual dimorphism of Alpheus colombiensisWicksten, 1988. The adult sex ratio was female biased, and solitary ovigerous females were found, suggesting a temporary mate guarding type of mating system. Our results also revealed sexual dimorphism on the snapping claw, which is larger in males than in females. The male’s snapping claw is probably under sexual selection, which can be mediated by male-male competition or female choice. We also estimated the A. colombiensis female size at maturity at 5.2 ± 0.76 mm. Our results contradict the common idea that snapping shrimps are monogamous species, and support that A. colombiensis probably have a temporary mate guarding (e.g., males can sexually interact with more than one female, in opposition to sexual monogamy). This study also sustains the growing evidence that alpheid shrimps display snapping claw sexual dimorphism.


2007 ◽  
Vol 85 (1) ◽  
pp. 92-98 ◽  
Author(s):  
C.M. Gienger ◽  
Daniel D. Beck

We tested the hypothesis that helodermatid lizards (Gila monsters, Heloderma suspectum Cope, 1869, and beaded lizards, H. horridum (Wiegmann, 1829)) show sexual dimorphism in morphological traits related to male–male agonistic behaviors. Male–male combat in helodermatid lizards involves repeated sequences of ritualized grappling. Male Gila monsters use their heads in attempts to gain or maintain a superior position during repeated combat bouts that may last for hours. Pairs of fighting male beaded lizards form spectacular body arches, with abdomens adpressed and snouts, forelimbs, and tail tips contacting the ground. We measured body size, head size, and tail length in 208 preserved H. suspectum, and body size and tail length (but not head size) in 79 live H. horridum, then tested for sexual dimorphism using analysis of covariance. Male Gila monsters had proportionately larger heads than females but did not differ in tail length or body size. Male beaded lizards had proportionately longer tails than females and were larger in body size only when the largest individuals were included in the analysis. Differences in head dimensions (in H. suspectum) and tail length (in H. horridum) are likely the result of sexual selection acting through male–male agonistic behaviors in this unique lizard taxon.


2021 ◽  
Vol 16 (1) ◽  
pp. 11-25
Author(s):  
Valeria De Olivera-López ◽  
Arley Camargo ◽  
Raúl Maneyro

Intersexual morphological differences within a species occur in many traits, including body size and shape. Many processes that cause geographic variability in morphology have been proposed: population structure, phenotypic plasticity (environmental effects on development), and natural and/or sexual selection. Several hypotheses can explain patterns of sexual dimorphism in anurans, including natural or intra/inter-sexual selection, and differences in life history strategies between sexes. Limnomedusa macroglossa is considered a habitat specialist restricted to rocky outcrops in Brazil, Argentina, Paraguay, and Uruguay. We evaluated the extent of sexual (size and shape) dimorphism in L. macroglossa from Uruguay based on morphometrics and secondary sexual characteristics, while taking into account geographic variation. Sexual dimorphism in body size of adults was found, but multivariate analyses did not demonstrate the existence of significant differences in shape. There were also significant differences in body size and hind leg measurements among six hydrographic basins as a result from the phenotypic plasticity correlated with local temperature, representing a clinal variation along the latitudinal gradient of Uruguay. The sexual dimorphism found in body size is probably the consequence of higher growth rates and/or late sexual maturity in females, which favors larger body size for accommodating larger ovaries, and thus, higher reproductive output. 


2017 ◽  
Vol 69 (1) ◽  
pp. 23-33 ◽  
Author(s):  
Bojan Ilic ◽  
Bojan Mitic ◽  
Slobodan Makarov

Apfelbeckia insculpta (L. Koch, 1867) is one of the largest European millipedes and an endemic species of the Balkan Peninsula. We present data on sexual dimorphism in size and body proportions obtained from 179 adult specimens of this species from four caves in Serbia and one in Montenegro using univariate and multivariate morphometric techniques. Sexual dimorphism was apparent and female-biased for all measured characters, except for lengths of the antennae and the 24th leg pair (which were larger in males) and lengths of the first, second and fourth leg pairs, which exhibited small differences between sexes. Generally, females had significantly greater body size than males, while males expressed significantly greater values in traits that can be associated with mobility and copulation behavior. Also, we found significant variations in sexual size and body proportions dimorphism among analyzed populations. The influences of fecundity and sexual selection on the adult body plan in A. insculpta are discussed.


2018 ◽  
Vol 32 ◽  
pp. 5-17
Author(s):  
Hadi Khoshnamvand ◽  
Mansoureh Malekian ◽  
Yazdan Keivany

Morphological differentiation and sexual dimorphism in the two genetically distinct clades (Northern and Southern clades) of the Lorestan newt, Neurergus kaiseri, was evaluated for 72 live specimens, using five body- and nine head-related characters and eight calculated ratios. Principle component analysis of morphological characters confirmed that the Lorestan newt populations are well separated into two distinct groups, suggesting that a taxonomic revision in N. kaiseri may be required because of significant molecular, morphological and ecological differences between these clades. Sexual dimorphism in N. kaiseri includes body size and shape. Females were clearly larger than males in most body- and head-related variables and males had relatively greater head width and eye length. Sexual dimorphism in this species may be linked to sexual selection and ecological differences between sexes. However, many aspects of the ecology and reproductive biology of this species remain unknown.


2016 ◽  
Vol 283 (1829) ◽  
pp. 20152830 ◽  
Author(s):  
David A. Puts ◽  
Alexander K. Hill ◽  
Drew H. Bailey ◽  
Robert S. Walker ◽  
Drew Rendall ◽  
...  

In many primates, including humans, the vocalizations of males and females differ dramatically, with male vocalizations and vocal anatomy often seeming to exaggerate apparent body size. These traits may be favoured by sexual selection because low-frequency male vocalizations intimidate rivals and/or attract females, but this hypothesis has not been systematically tested across primates, nor is it clear why competitors and potential mates should attend to vocalization frequencies. Here we show across anthropoids that sexual dimorphism in fundamental frequency ( F 0 ) increased during evolutionary transitions towards polygyny, and decreased during transitions towards monogamy. Surprisingly, humans exhibit greater F 0 sexual dimorphism than any other ape. We also show that low- F 0 vocalizations predict perceptions of men's dominance and attractiveness, and predict hormone profiles (low cortisol and high testosterone) related to immune function. These results suggest that low male F 0 signals condition to competitors and mates, and evolved in male anthropoids in response to the intensity of mating competition.


2001 ◽  
Vol 79 (6) ◽  
pp. 1016-1020 ◽  
Author(s):  
A I Schulte-Hostedde ◽  
J S Millar ◽  
G J Hickling

Differences in reproductive roles between the sexes may lead to sexual dimorphism in body composition. Body size and composition of three species of small mammals (bushy-tailed wood rats (Neotoma cinerea Ord), deer mice (Peromyscus maniculatus Wagner), and red-backed voles (Clethrionomys gapperi Vigors)) were analyzed to test the predictions that (i) males will have more muscle mass than females and (ii) females will have more fat than males. Results supported the first prediction but not the second. For all three species, males had more lean dry mass relative to body size than females, but females did not have relatively more fat than males. Muscle mass of males may aid in mate-searching and mate-guarding activities, but fat content may not differ between the sexes because female small mammals depend on increased ingestion rates, rather than fat stores, to support reproduction.


2010 ◽  
Vol 60 (4) ◽  
pp. 395-412 ◽  
Author(s):  
Peter Cunningham ◽  
Martin Plath ◽  
Torsten Wronski ◽  
Mohamed Sandouka

AbstractSexual selection can lead to sexual dimorphism, where elaborated traits used in mate attraction or weaponry are more expressed in the male sex. The degree of sexual dimorphism, however, is known to vary even among closely related taxa. Here we examined sexual dimorphism in horn length and three measures related to body size (body weight, shoulder height, and neck circumference) in four gazelle taxa, representing at least three species, i.e. Dorcas gazelle (G. dorcas), Sand gazelle (G. subgutturosa marica) and Mountain gazelle (G. gazella). The latter is represented by two distinctive phenotypes maintained and bred at the King Khalid Wildlife Research Centre in Saudi Arabia. We describe marked differences in sexual dimorphism among taxa. For example, the difference in sexually dimorphic horn development was driven primarily by females exhibiting pronounced differences in horn development. We discuss how divergent mating systems, and group sizes affect these differences among the examined taxa, with more competition in larger groups probably promoting the evolution of larger horns in females, thereby leading to less sexual dimorphism.


2009 ◽  
Vol 30 (1) ◽  
pp. 37-43 ◽  
Author(s):  
Attila Hettyey ◽  
Pierre-André Crochet ◽  
Juha Merilä ◽  
Gábor Herczeg ◽  
Anssi Laurila

AbstractVariation in colouration has rarely been related to sexual selection in anuran amphibians, even though such a relationship has been proven for many other vertebrate taxa. Male and female Moor Frogs (Rana arvalis) have a cryptic brown colour pattern, but males develop a conspicuous blue nuptial colouration during the reproductive season. To investigate the possibility that colouration plays a role in sexual selection in this species, we studied the temporal variation in blue colouration, determined if body size or body temperature affected blueness and investigated if blueness of males could be related to their mating success. Results confirmed previous observations that males develop and maintain blue colouration for only a very few nights during peak reproductive activity. Colouration of males was unrelated to body size, but males exhibiting higher body temperatures were somewhat bluer than males with lower body temperatures. Further, males in amplexus had higher body temperatures than non-mated males. Finally, mating success was positively related to blueness in small males, whereas in large males no such relationship was detected. While our results align with the hypothesis that the bright blue colouration of males may be a target of sexual selection, alternative explanations are also discussed.


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