Environmental influences on the sexual dimorphism in body size of western bobcats

Sexual size dimorphism might be influenced by environmental constraints on sexual selection or by intraspecific competition between males and females. We studied bobcats (Lynx rufus) in collections of museum specimens from western North America to examine these hypotheses. Structural body size was estimated from several measurements of the skull, ln-transformed and indexed through principal components analysis. Sexual dimorphism in body size was estimated from the difference in size index of males and females, and compared to geographic and climatic variables associated with biotic provinces (ecoregions). Of several climatic variables that were associated with bobcat body size, only seasonality of climate was associated with sexual dimorphism. Sexual size dimorphism, longitude, elevation, and seasonality were intercorrelated. As longitude decreased (moving inland from west-coastal ecoregions), sexual dimorphism decreased with the increased elevation and seasonality of continental climates of the Rocky Mountains. We suggest that increased seasonality and the need for fasting endurance by females may place constraints on the degree of sexual dimorphism in bobcats. Sexual dimorphism of body size and sexual size dimorphism of trophic structures (teeth) exhibited a strong positive association over geography, thus indirectly supporting the hypothesis that intrasexual competition for prey could account for the geographic variation in sexual size dimorphism. Thus, both environmental constraints on sexual selection of body size and intersexual competition were supported as possible explanations of the degree of sexual size dimorphism that occurs in populations of bobcats.     

Changes in the sexual dimorphism of the human mandible during the last 1200 years in Central Europe

According to many investigations, changes in mandibular morphology can occur synchronously with changes in the environment, and sexual dimorphism of the mandible can be influenced by the environment. Sexual dimorphism during the last 1200 years was evaluated using geometric morphometric analysis of virtual cranial models. The method of geometric morphometrics allows differences in size and shape to be assessed separately. We analyzed groups of adult individuals dating to Early Middle Ages, High Middle Ages, Early Modern Ages and from a modern Czech population (21st century). Significant sexual dimorphism in mandibular size was found in all populations. A trend in the sexual dimorphism of size was seen, with differences between the sexes increasing gradually over time. Size changes in female mandibles were a better reflection of environmental conditions and climate than size changes in male mandibles. Regarding changes in the sexual dimorphism of shape, significant dimorphism was found in all four samples. However, the pattern of mandibular shape dimorphism was different and varied considerably between samples. There was only one stable shape trait showing sexual dimorphism across all four samples in our study: the gonion lies more laterally in male than in female mandibles and male mandibles are relatively wider than female mandibles. Sexual dimorphism of shape is not influenced by the climate; instead sexual selection might play a role. This research supports earlier studies that have found that the degree and pattern of sexual dimorphism is population-specific and the factors regulating sexual dimorphism today may not be the same as those in the past.     

Sexual dimorphism in Ichneumonidae: a response to Hurlbutt

Sexual dimorphism in parasitoid wasps of the family Ichneumonidae is surveyed and the problems associated with its measurement are discussed. Conclusions drawn by Hurlbutt are demonstrated to be incorrect. The significance of sexual dimorphism in ichneumonids is explored briefly.     

Sexual dimorphism in the snub-nosed langurs (Colobinae: Rhinopithecus)

Sexual dimorphism in the dentition and skeleton of the four extant species of snub-nosed langurs, Rhinopithecus (R.) bieti, R. (R.) brelichi, R. (R.) roxellana and R. (Presbytiscus) avunculus, was studied. The species shared a similar general pattern of sexual dimorphism, but were found to differ in respects that appear to reflect the influence of disparate socioecological and environmental factors. All the species showed marked canine dimorphism, but the very high degree of canine dimorphism in R. bieti appeared to be due to the intensity of intermale competition for mates during a temporally restricted breeding season, and possibly also to the intensity of competition between males for other resources during other times of the year. Sexual dimorphism in the postcranial skeleton of Rhinopithecus species was also most pronounced in R. bieti and may be related to the relatively higher frequency of terrestrial locomotion in males of the species. © 1995 Wiley-Liss, Inc.     

Evolutionary allometry of sexual dimorphism of jumping performance in anurans

Evolutionary Ecology - Sexual dimorphism is a common feature in animals, yet the degree of sexual dimorphism is not constant across taxa. Sometimes the magnitude of sexual dimorphism varies...     

The evolution of sexually dimorphic tail feathers is not associated with tail skeleton dimorphism

Sexual selection can influence the evolution of sexually dimorphic exaggerated display structures. Herein, we explore whether such costly ornamental integumentary structures evolve independently or if they are correlated with phenotypic change in the associated skeletal system. In birds, elongate tail feathers have frequently evolved in males and are beneficial as intraspecific display structures but impart a locomotor/energetic cost. Using the sexually dimorphic tail feathers of several passeriform species as a model system, we test the hypothesis that taxa with sexually dimorphic tail feathers also exhibit sexual dimorphism in the caudal skeleton that supports the muscles and integument of the tail apparatus. Caudal skeletal morphology is quantified using both geometric morphometrics and linear morphometrics across four sexually dimorphic passeriform species and four closely related monomorphic species. Sexual dimorphism is assessed using permutational MANOVA. Sexual dimorphism in caudal skeletal morphology is found only in those taxa that exhibit active functional differences in tail use between males and females. Thus, dimorphism in tail feather length is not necessarily correlated with the evolution of caudal skeletal dimorphism. Sexual selection is sufficient to generate phenotypic divergence in integumentary display structures between the sexes, but these change are not reflected in the underlying caudal skeleton. This suggests that caudal feathers and bones evolve semi‐independently from one another and evolve at different rates in response to different types of selective pressures.     

The evolution of sexual size dimorphism in the house finch. III. Developmental basis

Sexual size dimorphism of adults proximately results from a combination of sexually dimorphic growth patterns and selection on growing individuals. Yet, most studies of the evolution of dimorphism have focused on correlates of only adult morphologies. Here we examined the ontogeny of sexual size dimorphism in an isolated population of the house finch (Carpodacus mexicanus). Sexes differed in growth rates and growth duration; in most traits, females grew faster than males, but males grew for a longer period. Sexual dimorphism in bill traits (bill length, width, depth) and in body traits (wing, tarsus, and tail length; mass) developed during different periods of ontogeny. Growth of bill traits was most different between sexes during the juvenile period (after leaving the nest), whereas growth of body traits was most sexually dimorphic during the first few days after hatching. Postgrowth selection on juveniles strongly influenced sexual dimorphism in all traits; in some traits, this selection canceled or reversed dimorphism patterns produced by growth differences between sexes. The net result was that adult sexual dimorphism, to a large degree, was an outcome of selection for survival during juvenile stages. We suggest that previously documented fast and extensive divergence of house finch populations in sexual size dimorphism may be partially produced by distinct environmental conditions during growth in these populations.     

Sexual dimorphism inSebastes

Synopsis Sexual dimorphism and factors that may cause it were investigated in 34 species of the genusSebastes. Sexual dimorphism in standard length and morphometric characters are fairly common in rockfish. In many species males are shorter than females. However in males head length, width of orbit, interorbital width, length of upper jaw, longest pectoral fin ray and longest dorsal spine tend to be larger at a specified size than in females. Water-column species tend to be more dimorphic than demersal species. We suggest that the observed differences in dimorphism in standard length may be related to differences in mating and territorial behavior. Dimorphisms in morphometric measurements may be related to compensation in feeding ability for reduced standard length of males, mating and territorial behavior.     

Seasonal change in sexual size dimorphism of the major cheliped in the hermit crab <Emphasis Type="Italic">Pagurus minutus</Emphasis>

Sexual size dimorphism is a common phenomenon in the animal kingdom, and its seasonal change has been reported in some species that possess traits dimorphic only in males and specialized for male mating success. However, few studies have examined seasonal change in sexual dimorphism of traits possessed by both sexes. Here, we examined the reproductive biology of the hermit crab Pagurus minutus, at a sandflat in the Waka River estuary, Japan, with special reference to seasonal changes in sexual dimorphism of the large claw (major cheliped) size by conducting population and precopulatory guarding-pair sampling. Previous investigation demonstrated that the major cheliped is used as a weapon, and its size, more than body size, determines the winner in male–male contests of this species. We found ovigerous females from November to April, peaking in January, when 80% of females were ovigerous. Sexual size dimorphism of the major cheliped was observed; the degree of dimorphism increased in the reproductive season, when only males possessed an enlarged major cheliped. In addition, in the reproductive season, precopulatory guarding males had a larger body and larger relative size of the major cheliped than did solitary males, although the major cheliped size in guarding males seemed to reach an upper limit. These results suggest that seasonal change in sexual dimorphism of the major cheliped size in P. minutus strongly reflects sexual selection favoring the development of this natural weaponry, and that the degree of the dimorphism might be limited through natural selection.     

Changes in the sexual dimorphism of triatominae in the transition from natural to artificial habitats.

A shift from large to small average sizes was observed in Triatoma infestans and Rhodnius domesticus between field and domestic (or laboratory) conditions of life. It was more pronounced in the female specimens, leading to a subsequent reduction of sexual size dimorphism. This feature is discussed in terms of genetic and populational changes occurring from natural to artificial habitats, in particular those related to population densities. Sexual size dimorphism is then recommended as a new character to be used in the study of species of Triatominae adapting to domestic ecotopes.     

A note on the evolution of sexual dimorphism

Sexual dimorphism is discussed as a diffusion problem. The establishment of different gametic size is favoured through Brownian motion.     

Why are American mink sexually dimorphic? A role for niche separation

American mink are highly sexually dimorphic, with males being up to twice the size of females. Sexual dimorphism may arise for several reasons, including intra- or inter-sexual selection, inter-sexual competition, or divergent reproductive roles. Whether or not dimorphism arises from competition, a degree of niche separation is expected in dimorphic species. Sexual divergence in feeding niche has been reported for many species, including mink. This is likely to be manifested in a greater degree of dimorphism in those structures, such as teeth, that are used for the acquisition of prey. We tested the hypothesis that teeth and other trophic structures of male mink would be significantly larger than those of females, after controlling for underlying skeletal size differences. Canine and carnassial teeth, and several skull dimensions, were larger than predicted in males. There is good evidence that sexual dimorphism in mink trophic apparati is greater than predicted from allometry. We examined the development of dimorphism in various features with age and found that it was not consistent. Several trophic features were dimorphic amongst juveniles, and the degree of dimorphism remained relatively constant with age. Dimorphism in canines, and in relative body mass, was less apparent amongst juveniles and increased with increasing age. We discuss our results in the light of contemporary theories on the evolution and maintenance of sexual size dimorphism and argue that niche separation as a result of dimorphism in trophic features, while probably not the driving force behind sexual size dimorphism, may play a role in its maintenance.     

The autumn movements of the Woodpigeon

Sexual dimorphism of 2 plumage features and some morphological measurements was assessed in a sample of 140 museum skins and over 300 wild-trapped Coal Tits Parus ater britannicus. All the characters examined displayed highly significant sexual dimorphism, and have allowed the presentation of a recommended methodology which should allow over 90% of all British Coal Tits to be sexed correctly by fieldworkers. The validity of year-round sexing using characteristics of the throat feathering is proven by comparison with the results of a molecular DNA sexing technique.     

Sexual selection mediated by the thermoregulatory effects of male colour pattern in the ambush bug Phymata americana

Sexual dimorphism in coloration is a taxonomically widespread phenomenon often attributed to sexual selection on visual signals. However, the ambush bug Phymata americana exhibits sexual dimorphism in coloration that has no apparent signalling function. Here we provide evidence that colour pattern in this species influences male mating success indirectly through its effect on thermoregulation. We demonstrate, using experimental manipulation, that individuals with dark colour pattern achieve higher thoracic temperatures under illumination. We also show that dark colour pattern predicted mate-searching success but only under thermally challenging conditions (i.e. cool ambient temperature). As far as we are aware, this is the first study to provide evidence that sexual dimorphism can be accounted for by sexual selection on thermoregulatory performance.     

Evolution of sexual dimorphism of wing shape in the Drosophila melanogaster subgroup

Background  

Sexual dimorphism of body size has been the subject of numerous studies, but few have examined sexual shape dimorphism (SShD) and its evolution. Allometry, the shape change associated with size variation, has been suggested to be a main component of SShD. Yet little is known about the relative importance of the allometric and non-allometric components for the evolution of SShD.     

Variation in Craniomandibular Morphology and Sexual Dimorphism in Pantherines and the Sabercat Smilodon fatalis

Sexual dimorphism is widespread among carnivorans, and has been an important evolutionary factor in social ecology. However, its presence in sabertoothed felids remains contentious. Here we present a comprehensive analysis of extant Panthera and the sabertoothed felid Smilodon fatalis. S. fatalis has been reported to show little or no sexual dimorphism but to have been intraspecifically variable in skull morphology. We found that large and small specimens of S. fatalis could be assigned to male and female sexes with similar degrees of confidence as Panthera based on craniomandibular shape. P. uncia is much less craniomandibularly variable and has low levels of sexual size-dimorphism. Shape variation in S. fatalis probably reflects sexual differences. Craniomandibular size-dimorphism is lower in S. fatalis than in Panthera except P. uncia. Sexual dimorphism in felids is related to more than overall size, and S. fatalis and the four large Panthera species show marked and similar craniomandibular and dental morphometric sexual dimorphism, whereas morphometric dimorphism in P. uncia is less. Many morphometric-sexually dimorphic characters in Panthera and Smilodon are related to bite strength and presumably to killing ecology. This suggests that morphometric sexual dimorphism is an evolutionary adaptation to intraspecific resource partitioning, since large males with thicker upper canines and stronger bite forces would be able to hunt larger prey than females, which is corroborated by feeding ecology in P. leo. Sexual dimorphism indicates that S. fatalis could have been social, but it is unlikely that it lived in fusion-fission units dominated by one or a few males, as in sub-Saharan populations of P. leo. Instead, S. fatalis could have been solitary and polygynous, as most extant felids, or it may have lived in unisexual groups, as is common in P. leo persica.     

Sexual dimorphism in response to herbivory and competition in the dioecious herb Spinacia oleracea

Plant Ecology - Sexual dimorphism is common in dioecious plant species and is usually attributed to different cost of reproduction associated with male and female functions. Differences in growth...     

Sexual dimorphism in the long term speech spectrum

Long-term speech sound spectra of 82 female and 58 male students were computed digitally. Sexual dimorphism of the spectra became apparent by 3 statistical methods: multidimensional scaling of overall similarity data, analysis of variance and discriminant analysis. The spectral amplitude distribution between 80 and 300 Hz showed the highest dimorphism, due to differences in the mean fundamental frequency caused by the larynx. Also frequency regions above 1 kHz contain marked dimorphism leading to an automatic sex recognition rate of 87%. This second dimorphism is mainly caused by the vocal tract resonance. A hypothesis is presented in which these two independent dimorphic structures are compared with consideration to their phylogenetic age.     

On the sexual dimorphism in the skull of the tiger (Panthera tigris)

Sexual dimorphism in the skull of the tiger (Panthera tigris) is reviewed and described in detail. The most significant diagnostic differences between the sexes are absolute length of the cranium, breadth of interorbital region and muzzle, zygomatic arch, and occipital region, length of upper carnassial, and the degree of the development of the cranial prominences. The degree of sexual dimorphism is closely related to geographic variation, and its form is rather complex.     

Processes that constrain and facilitate the evolution of sexual dimorphism

Sexual dimorphism, or differences between the sexes, is pervasive in both plants and animals despite genetic and developmental constraints on its evolution. This special issue of the American Naturalist, which is based on the annual Vice Presidential Symposium, documents how the underlying processes responsible for the presence and extent of sexual dimorphism can be qualified and quantified by a variety of approaches. These include estimates of the G matrix and phenotypic selection, artificial selection, phenotypic manipulation of hormones, estimates of sex-differential sensitivity to maternal effects, among-population and phenotypic plasticity studies, and the mapping of sexual dimorphism onto a phylogeny. The questions addressed in the articles in this issue vary depending on the motivation for the studies and the taxa being investigated, but taken together, they show how the integration of genetic, developmental, physiological, ecological, and phylogenetic approaches can illuminate the processes underlying the evolution of sexual dimorphism.