Age-associated male mating success in three swarming caddis fly species (Trichoptera: Leptoceridae)

Abstract. 1. In the three caddis fly species, Athripsodes albifrons (L.), A. cinereus (Curtis) and Mystacides azurea (L.) (Leptoceridae; Trichoptera), males swarm above the water surface of lakes or rivers. Receptive females fly to swarms and are chased and/or courted by males. After one of the swarming males has grasped an approaching female, the pair flies in tandem to the shore where they copulate.
2. In males, wing wear indices were negatively correlated with the ratio of fat/dry weight. In the only species in which comparisons were possible between newly emerged and swarming males (M. azurea), the former had significantly lower indices. Unmated females on average had lower wing wear indices than spent females. These facts suggest that wing wear reflects relative age.
3. The tandem males had significantly less wing wear than those in swarms, and are probably therefore younger. Age is therefore likely to be significant in relation to mating success.
4. Among males of the same relative age, tandem males had higher fat ratio than swarming ones, indicating that male mating success was also influenced by traits other than age. It is suggested that the shortest possible duration of the period of adult prematurity is adaptive, especially in insects with marginal adult food intake.     

Wing-scales of Pseudoleptocerus chirindensis Kimmins (Trichoptera: Leptoceridae)

The African species Pseudoleptocerus chirindensis belongs to a small group of Trichoptera most unusual in having scaly wings. Electron microscope studies reveal 13 structurally distinct kinds of cuticular process on the wings, including several types of squamiform and hair-like macrotrichia. These are described in detail and their possible functions inferred. The optical properties of the scales forming the colour pattern of the forewings are related to ultrastructural elements including diffraction and thin film interference systems. Trirhopteran scale structure is compared with that of the Lepidoptera, the sister-group in the Amphiesmenoptera. Differences are found and it is tentatively concluded that wing-scales have evolved independently in the two orders.     

A new species of Amphoropsyche (Trichoptera, Leptoceridae) from Ecuador, with a key to the species in the genus

A new species of Amphoropsyche Holzenthal is described from Ecuador. It is similar to a group of species with dorsomesal processes on the preanal appendages (i.e., Amphoropsyche woodruffi Flint & Sykora, Amphoropsyche refugia Holzenthal, and Amphoropsyche aragua Holzenthal), but can be distinguished from these and other members of the genus by the short, digitate dorsomesal processes on the preanal appendages and the broad lateral processes of tergum X of the male genitalia. A key to males of the 14 species now known in the genus is presented based on characters of the genitalia.     

Sexual size dimorphism and reproductive ecology in relation to mating system in waders

The relationship between sexual size dimorphism, body-weight and different reproductive traits (e.g. clutch size, egg weight and incubation period) in relation to mating system and forms of parental care was studied in waders. Two hypotheses were examined. (1) Sexual size dimorphism is correlated with the intensity of sexual selection. (2) The degree of sexual size dimorphism is the result of an interrelationship between the reproductive strategy of the female and her body size. In the polygynous species the male was significantly larger than the female. This is consistent with the sexual selection hypothesis. However, among waders, a positive correlation exists between egg weight, clutch mass and body-weight. Selection for small eggs or a short incubation period may therefore have an influence on female body-weight. If the lack of paternal care reduces the female's possibility for producing large eggs or incubating a large clutch mass, we would expect a selection pressure for small female size among polygynous species. Thus, large sexual size dimorphism among polygynous waders may be a result of selection for small female size to lack of paternal care, or selection for large male size due to intramale competition or a female preference for large-sized males. In multiple-clutch species (viz. species in which the female regularly lays more than one clutch during the season) egg weight was low both for a given female and male body-weight. The low egg weight of multiple-clutch species is assumed to be a result of the constraints placed on the female from producing several clutches during a single breeding season.     

Sexual dimorphism and sexual conflict in the diving beetle Agabus uliginosus (L.) (Coleoptera: Dytiscidae)

Sexual conflict can drive intersexual arms races, with female resistance and male persistence traits coevolving antagonistically. Such arms races are well documented in some diving beetles, although the extent of sexual conflict in this family remains unclear. The European dytiscid Agabus uliginosus has a strikingly dimorphic female; individuals from most regions are smooth and male‐like, whereas those from some populations have a strongly roughened dorsum, a trait that has attracted the name dispar. We demonstrate that rough and smooth females differ consistently in the development of dorsal surface microreticulation, and that these females are associated with males that differ in the development of their persistence traits. These findings extend the occurrence of pre‐insemination sexual conflict and associated intrasexual dimorphism in Dytiscidae, and suggest that such mating systems are relatively widespread in these beetles.     

Sexual dimorphism and mating systems: jumping to conclusions

Previous studies have suggested that there is a strong relationship between a high degree of aggressive competition among males for access to fertile females and large body and canine size in males. It has further been suggested that such a relationship among living primates can be used to infer the social organization of extinct primate species from the degree of sexual dimorphism exhibited. Our field studies of patas (Erythrocebus patas) and blue monkeys (Cercopithecus mitis), two species which had previously been characterized as having one-male ‘harem’ group structures, indicate considerable variability in mating systems. We suggest, on the basis of our observations of these species, that factors other than male-male competition (e.g., predation) may also have influenced the degree of dimorphism in primates.     

Phylogeny of Grumichellini Morse, 1981 (Trichoptera: Leptoceridae) with the description of a new genus from southeastern Peru

Osflintia manu, new genus, new species, of long-horned caddisfly (Leptoceridae: Triplectidinae: Grumichellini) is described and illustrated from southeastern Peru. The phylogeny of Grumichellini Morse (Leptoceridae: Triplectidinae) is revisited and hypotheses of homology of some morphological characters are reconsidered. The monophyly of the tribe is corroborated and the phylogenetic relationships of its included genera are inferred to be (Triplexa (Gracilipsodes ((Grumichella, Amazonatolica) (Atanatolica, Osflintia, n. gen.)))) from adult and larval characters. Diagnostic characters of the new genus include the following: reduced tibial spur formula (2, 2, 2), loss of forewing crossvein sc-r1, hind wing discoidal cell closed, hind wing fork IV present, pair of long setae on tergum IX of the male genitalia, and pair of processes on the apex of segment X.     

Precopulatory mating behavior and sexual dimorphism in the amphipod Crustacea

Accounts in the literature of precopulatory mate-guarding in gammaridean amphipods are that males use one of two strategies for mating: either they mate-guard by carrying or attending their mates until they are ready to molt and be fertilized, or they do not guard, instead searching benthically or swarming pelagically at the time that females are ready to molt. Mate-guarding by carrying has been documented for species of the superfamilies Gammaroidea, Talitroidea, and Hadzioidea. Mate-guarding by attending has been found in the more sedentary Corophioidea and Caprellidea. Non-mate-guarders that search pelagically are species of Ampeliscoidea, Lysianassoidea, Phoxocephaloidea, Oedicerotoidea, and Pontoporeioidea. Non-mate-guarders that mate-search benthically are species of Eusiroidea, Crangonyctoidea, and Haustorioidea. Mate-guarding and non-mate-guarding males develop different secondary sex characters at maturity. Mate-guarding males have enhancements for fighting and signalling. These alterations are more elaborate in males that attend their mates than in males that carry their mates. Non-mate-guarders that search pelagically develop enhancements for swimming and sensing. Non-mate-guarders that remain benthic exhibit little change at maturity. Most mate-guarding males develop their secondary sexual characters over several molts and mate over more than one instar. Pelagic mate-searchers develop their secondary sexual characters at the last molt and mating is confined to the last instar. Females of most mate-guarding species are iteroparous, while fewer than half of non-mate-guarding species are so. It is hypothesized that mate-guarding arose more than once in the evolutionary history of amphipod Crustacea.     

Sexual dimorphism in calanoid copepods: morphology and function

Mate location and recognition are essentially asymmetrical processes in the reproductive biology of calanoid copepods with the active partner (the male) locating and catching the largely passive partner (the female). This behavioural asymmetry has led to the evolution of sexual dimorphism in copepods, playing many pivotal roles during the various successive phases of copulatory and post-copulatory behaviour. Sexually dimorphic appendages and structures are engaged in (1) mate recognition by the male; (2) capture of the female by the male; (3) transfer and attachment of a spermatophore to the female by the male; (4) removal of discharged spermatophore(s) by the female; and (5) fertilization and release of the eggs by the female. In many male calanoids, the antennulary chemosensory system is enhanced at the final moult and this enhancement appears to be strongly linked to their mate-locating role, i.e. detection of sex pheromones released by the female. It can be extreme in calanoids inhabiting oceanic waters, taking the form of a doubling in the number of aesthetascs on almost every segment, and is less expressed in forms residing in turbulent, neritic waters. Mate recognition is a process where chemoreception and mechanoreception presumably work in conjunction. The less elaborate male chemosensory system in the Centropagoidea is counterbalanced by females playing a more active role in generating hydromechanical cues. This is reflected in females in the shape of the posterior prosomal margin, the complexity of urosomal morphology and the size of the caudal setae. Visual mate recognition may be important in the Pontellidae, which typically show sexual dimorphism in eye design. The most distinctive sexual dimorphism is the atrophy of the mouthparts of non-feeding males, illustrating how copepod detection systems can be shifted to a new modality at the final moult. In the next phase, the male captures the female using the geniculate antennule and/or other appendages. Three types of antennulary geniculations are recognized, and their detailed morphology suggests that they have originated independently. Grasping efficiency can be enhanced by the development of supplemental hinges. The scanty data on capture mechanisms in males lacking geniculate antennules are reviewed. It is suggested that the loss of the antennulary geniculation in many non-centropagoidean calanoids has evolved in response to increasing predator pressure imposed on pairs in amplexus. Spermatophore transfer and placement are generally accomplished by the modified leg 5 of the male. In some males, leg 5 consists of both a chelate grasping leg and a spermatophore-transferring leg, whereas in others, only the latter is developed. Tufts of fine setules/spinules and/or sclerotized elements on the terminal portion of the leg are involved in the transfer and attachment of the spermatophore. The configuration of gonopores, copulatory pores and their connecting ducts in the female genital double-somite is diversified in the early calanoid offshoots such as Arietellidae and Metridinidae, whereas in more derived groups, it is constant and invariable, with paired gonopores and copulatory pores located beneath a single genital operculum. The absence of seminal receptacles in most Centropagoidea limits the female's ability to store sufficient sperm for multiple egg batches, suggesting that repeated mating is necessary for sustained egg production. Discharged spermatophores are usually removed by the female leg 5 and/or specialized elements on other legs. In Tortanus (Atortus) Ohtsuka, which has rudimentary fifth legs in the female and complex coupling devices in the male, a spermatophore supposedly remains on the female urosome, since eggs appear to be released from a ventral opening of the spermatophore. The type of sexual dimorphism is closely related to habitat and biology. Some hyperbenthic families never show multiplication of aesthetascs on the male antennule, whereas families of the open pelagic realm such as the Aetideidae always have non-feeding males exhibiting secondary multiplication of antennulary aesthetascs. The various aspects and diversity of calanoid sexual dimorphism are herein considered in an evolutionary context.     

Male load-lifting capacity and mating success in the swarming caddis fly Athripsodes cinereus

Abstract. Males of the caddis fly Athripsodes cinereus (Curtis) (Trichoptera: Leptoceridae) swarm above the water surface of lakes and streams. Females enter swarms and are pursued until grasped by a male. The pair couple their genitalia in the air, and then the male alone flies the pair to the shore where they settle and complete the copulation. About 8% of the pairs (total n = 384 pairs) dipped in the water soon after the coupling manoeuvre and about 25% of those then separated. Males in dipping pairs ( n = 13) were on average smaller and relatively older than the males that successfully carried their mate to the shore ( n = 54). No differences were found for flight muscle ratio (weight of flight muscles/total body weight) or relative load (total load/flight muscle weight). Males were larger than females (wing length), though typically female Trichoptera are the larger sex. Large male body size in A. cinereus may be an adaptation for flight during pairing; i.e. larger males are more likely to be able to carry larger loads.     

Sexual size dimorphism and assortative mating in Carolina Wrens

ABSTRACT.   Sexual size dimorphism (SSD) may be due to sexual and natural selection, but identifying specific mechanisms that generate such dimorphism in a species is difficult. I examined SSD in Carolina Wrens ( Thryothorus ludovicianus ) by examining (1) the degree of SSD in the population and between pairs using five morphometrics, (2) assortative mating patterns based on size and age, and (3) relationships between size and longevity. Analysis revealed that males were significantly larger than females in all body measurements. For example, mass, bill, and wing measurements yielded a canonical variable that permitted separation of the sexes and linear classification functions correctly determined the sex of 95% (238/250) of all wrens measured. No evidence was found to suggest that SSD was related to resource partitioning. However, assortative mating trends based on morphometrics (e.g., wing length), positive associations between longevity and morphometrics (e.g., wing length in females and body size in males), and intense male-male contests for territorial resources year-round provide evidence that sexual selection may contribute to SSD in Carolina Wrens.     

Sexual dimorphism and dichromatism in Steere's Liocichla (Liocichla steerii)

ABSTRACT.   Although sexual differences in birds can be extreme, differences between males and females in body size and plumage color are more subtle in many species. We used a genetic-based approach to determine the sex of male and female Steere's Liocichla ( Liocichla steerii ) and examine the degree of size dimorphism and plumage dichromatism in this apparently monomorphic species. We found that males were significantly larger than females. In addition, Steere's Liocichla have a prominent yellow plumage patch on the lores that was significantly larger in males than females for both live birds and museum specimens. We also used reflectance spectrometry to quantify the color of the yellow-green breast feathers of Steere's Liocichla and found no significant differences between males and females in brightness, intensity, saturation, or hue. However, females tended to have brighter breast plumage, particularly at long wavelengths. Collectively, these color variables were useful in discriminating birds according to sex when used in a discriminant function analysis. Our study suggests that sexual selection may be more widespread than once assumed, even among birds considered monomorphic, and emphasizes the need for additional data from tropical and subtropical species.     

Sexual selection explains Rensch's rule of allometry for sexual size dimorphism

In 1950, Rensch first described that in groups of related species, sexual size dimorphism is more pronounced in larger species. This widespread and fundamental allometric relationship is now commonly referred to as 'Rensch's rule'. However, despite numerous recent studies, we still do not have a general explanation for this allometry. Here we report that patterns of allometry in over 5300 bird species demonstrate that Rensch's rule is driven by a correlated evolutionary change in females to directional sexual selection on males. First, in detailed multivariate analysis, the strength of sexual selection was, by far, the strongest predictor of allometry. This was found to be the case even after controlling for numerous potential confounding factors, such as overall size, degree of ornamentation, phylogenetic history and the range and degree of size dimorphism. Second, in groups where sexual selection is stronger in females, allometry consistently goes in the opposite direction to Rensch's rule. Taken together, these results provide the first clear solution to the long-standing evolutionary problem of allometry for sexual size dimorphism: sexual selection causes size dimorphism to correlate with species size.     

Sexual size dimorphism in Ophisops elegans (Squamata: Lacertidae) in Iran

Twenty-three morphological features of 140 specimens of Ophisops elegans were analysed in order to identify sexual dimorphism in west and northwestern populations of Iran. Sexual dimorphism is significant (P<0.05) in nearly all metric features except for trunk length (TL) and length of widest part of belly (LWB), and in only two meristic characters, the number of dorsal scales around mid-body (DSN) and the number of femoral pores (FPN). Males have a relatively longer snout-vent length (SVL) than females and males have generally relatively larger heads compared to females.     

Sexual dimorphism of the Weberian apparatus and pectoral girdle in Sundadanio axelrodi (Ostariophysi: Cyprinidae)

The miniature cyprinid fish, Sundadanio axelrodi , exhibits extreme sexual dimorphism in the skeleton of the Weberian apparatus, the fifth rib and pectoral girdle. Musculature associated with the fifth rib and Weberian apparatus also shows a high degree of sexual dimorphism. It is suggested that these modifications are responsible for the production of a croaking sound that seems to be restricted to males of the species, based on the lack of any corresponding anatomical specializations in females.     

Sexual behaviour and evolution of sexual dimorphism in body size in Jaera (Isopoda Asellota)

Individuals of the genus Jaera do not mate at random. In the species from the Mediterranean group, J. italica and. J. nordmanni, large males and medium sized females are at an advantage and their sizes are positively assorted. These effects are attributable to sexual competition between males. In the Ponlo-caspian species J. istri, no advantage of large males exists, but sexual selection could be the cause for a long passive phase prior to copulation and for normalizing selection upon female size at pairing. In the Atlantic species, J. albifrons, no selection can be ascertained.
Differential mating success in males appears as one of the causes of the evolution of sexual dimorphism in body size, which makes males larger, of equal size, or smaller than females according to the species. The reason for this reversal in dimorphism seems to differ in the two sexes. Sexual selection provides an explanation for the evolution of male size, while the interspecific changes in female length are more likely due to ecological factors.     

Sexual dimorphism in growth from 8 to 18 years

A mixed longitudinal study of growth and development has been conducted, centering on an analysis of differences based on sex between the ages of 8 and 18 years for a series of 12 anthropometric indicators. The sample consisted of 50 girls and 63 boys. Proceeding from the specific differences, the variables can be divided into four groups with identical structures of differences. The first group comprises measurements of body height, body mass, shoulder width and pelvic span, all of which have higher values in boys between 8 and 10 and between 14 and 18. Between the ages of 11 and 13 girls are taller, heavier, with broader shoulders and pelvises. The second group covers measurements of subcutaneous fat. which are higher for girls throughout the period under review. The third group of indicators comprises the diameters of the joints of the extremities, i.e. of elbows and knees. Throughout the period under observation, these measurements are higher in boys, with the absolute differences between the sexes being the same at the age of 8 and ten years later. The fourth group consists of circumferences measurements of the extremities. It was found that calf circumferences manifested a specific inversion of the curves between 14 and 15, with girls showing a larger calf circumference up to the age of 14, and boys from the age of 15. The effect of earlier onset of puberty in girls was found to be reflected only on the inversion of the curve flow of the variables from the first group.     

Sexual dimorphism in Champsosaurus (Diapsida, Choristodera)

Two nearly complete specimens of Champsosaurus (Diapsida, Choristodera) with distinctive morphologies, from the Tullock Formation (Early Paleocene) of northeastern Montana, USA, were described as different species. The limb bones of C. ambulator are more robust than those of C. laramiensis, indicating that C. ambulator was more adapted for walking than C. laramiensis. The phylogenetic significance of these limb bone morphologies, however, appears questionable because similar dimorphic variations occur in a closely related genus and champsosaurs from other geologic ages and locations. Female champsosaurs may have been better adapted to a terrestrial life than males due to nesting behavior on land, resulting in variable limb bone morphologies between sexes. The observed morphologic variations are, hence, hypothesized to reflect sexual dimorphism rather than sympatry of species. The C. ambulator-shaped humeri and femora, demonstrating a terrestrial adaptation, are suggested to belong to females and C. laramiensis-shaped limb bones to males. No significant variations of humeral and femoral morphologies occur in small champsosaur specimens, suggesting an aquatic niche for juveniles like adult males.