Swarming Behavior, Sexual Dimorphism, and Female Reproductive Status in the Sex Role-Reversed Dance Fly Species Rhamphomyia marginata

Dance flies are predaceous insects which often form male mating swarms. In many species males prior to swarming catch an insect prey, which is presented to the female at mating. In Rhamphomyia marginata, females in contrast to males gather to swarm, while males carrying a prey visit swarms for mating. Here I describe the swarming and courtship behavior in R. marginata and provide data on sexual dimorphism and swarming female reproductive status. Females swarm in small clearings in the forests. There was no specific swarm-maker. The swarming period lasted for 2–3 h and peaked around sunset. Identical swarm sites were used each evening and for several years. The mean number of females in swarms (swarm sites with at least one female) was 9.9 ± 9.1 (range, 1–40; n = 107) in 1993 and 7.1 ± 7.0 (range, 1–35; n = 68) in 1994. No obvious competition between females in swarms was observed. The operational sex ratio in swarms was extremely female biased (all swarms, 0.04). Less than one-third of male visits to swarms resulted in mating and males were found more often in larger swarms. Nuptial prey consisted of male midges. Females seem to mate more than once. Swarming females had undeveloped eggs, whereas mated females in swarms had further developed eggs than unmated females. Amount of sperm in the spermatheca was correlated with egg size. Amount of sperm and egg size did not correlate with wet weight, wing length, or wing load, except for egg size and weight. The wing coloration pattern and shape in R. marginata females are unique among dance flies, being greatly enlarged (1.6 times larger than that of males) and bicolored (gray part, 60% of wing area). When females, instead of males, possess extravagant secondary sexual characters, it is predicted from sexual selection theory that females should compete for males and that males should be selective in their choice of partner. A sex-role reversal will evolve when assess to males limit female reproductive success. The dance fly species R. marginata, like Empis borealis, another dance fly species studied earlier and discussed here, seems to fit these predictions.     

Mating system ofTokunagayusurika akamusi (Diptera: Chironomidae): I. Copulation in the air by swarming and on the ground by searching

Observations on the mating system of the midge,Tokunagayusurika akamusi, revealed mating to occur both in the air by swarming and on the ground by searching. At the shores of Lake Biwa, midges appeared from November to early December. Newly emerged adults arrived at the resting place, lakeside vegetation, in the morning, during which time a number of males also walked about in search of mates. Many copulating pairs were observed at the resting place. Huge swarms occurred chiefly before sunset but the frequency of copulation observed in the swarm was extremely low. It is likely that, in the Lake Biwa population, the proportion of females inseminated by searching males at the resting place was much larger than that by swarming males in the air. Furthermore, by searching, males copulated with younger females than by swarming. The differences between the searching and swarming tactics are discussed.     

Male mating success,sexual size dimorphism,and site fidelity in two species of Malacoctenus (Labrisomidae)

Synopsis In both Malacoctenus hubbsi and Malacoctenus macropus, males defended preferred oviposition sites from both other males and potential egg predators. In M. hubbsi, adult females were larger than adult males. Larger M. hubbsi males were not associated with territory parameters that were correlated with higher mating success, and male size was not correlated with mating success. Male size did affect mating success when territory parameters were statistically controlled for, but the failure of large males to associate with better territories eliminated any mating advantage for larger males. In M. macropus, males are larger than females. Larger males defended preferred oviposition sites, and had higher mating success than did smaller males. Male M. macropus also had much higher site fidelity than male M. hubbsi. These results suggest that the evolution of the differences in site fidelity and sexual size dimorphism between these two species may be due to sexual selection acting differentially in these two species.     

Swarming and mating behaviour ofChironomus flaviplumus (Diptera: Chironomidae), compared with a sympatric congeneric species,C. yoshimatsui

The swarming and mating behaviour ofChironomus flaviplumus was observed and compared with a sympatric congeneric species,C. yoshimatsui. C. flaviplumus males swarmed around sunset near foliage or angles of buildings near the emergence site and copulated with females entering the swarm. Swarming and mating occurred under conditions of higher light intensity in cooler seasons than in warmer ones. Results suggested that temperature had an effect on the timing of flight to the swarming site in both sexes. TheC. flaviplumus swarm marker and swarming behaviour seemed very similar to that toC. yoshimatsui, and their respective daily swarming time zone greatly overlapped. No mixed swarm, however, was observed in the study area. This is probably due to the distance between the species' larval habitats. Possible premating isolation mechanisms between these 2 species are discussed.     

Non-random Mating in the Dance Fly Empis borealis: The Importance of Male Choice

In the dance-fly Empis borealis (Diptera, Empididae), females form swarms to which males, carrying a nuptial gift, come for mating. We examined whether males or females were choosy and/or competed for mates. First, measurements of the size relationships between copulating males and females, nuptial gifts and the swarming females from different swarms were assessed. Second, male visiting time in differently sized female swarms was recorded. Larger (wing-length) females participated disproportionately in copulations in each swarm, but not for the population at large. Female mating status (virgin/non-virgin) or proximity to oviposition (egg size) did not influence the likelihood of copulation. No assortative mating pattern was found: male size and size of nuptial gift did not correlate with size of the mating female. The time spent by males in swarms increased with the number of females present and it took longer when males left a swarm without copulation than when doing so. Male visiting time per female was negatively correlated with number of females in swarms. Males more often left smaller than larger swarms without mating. We conclude that E. borealis males discriminate among females but find no evidence for male competition or for female choice. It is still a question to what degree females compete for males.     

Swarm Site Fidelity in the Sex Role-Reversed Dance Fly Empis borealis

In the dance fly species Empis borealis (L.), females (1–40) gather to swarm at landmarks (swarm markers, like trees and bushes), and males carrying an insect prey visit these swarms for mating. We noticed earlier that some swarm sites were used for several years and that they appeared to be frequented by a similar number of swarming females in each year, although the numbers of females varied greatly among swarm sites and certain sites attracted more swarming individuals than others. To explore swarm site fidelity in this mating system, in 1993 we monitored the same swarm sites that we studied in 1989, addressing the questions, Would the same swarm sites still attract the same number of females and males after 4 years? and Why do some swarm sites attract more displaying females than others? The number of females swarming at the different markers in 1993 was approximately the same as 4 years earlier. Some of these swarm sites are known to have been used for 18 years. The swarm sites with the largest number of flies had a high sun exposure during the day and were found at coniferous swarm marker trees and in a mixed forest habitat. A swarm site with few females attending and with a low amount of insolation during the day can be predicted to be abandoned as a swarming site soon. Empis borealis swarm sites thus persist over many years and are attended by a similar number of individuals each year. To our knowledge, such site fidelity has not been demonstrated for any swarming insect species earlier.     

Mating Aggregations and Mating Success in the Flower Thrips, Frankliniella schultzei (Thysanoptera: Thripidae), and a Possible Role for Pheromones

Aggregations of Frankliniella schultzei males were observed on the corollas of Hibiscus rosasinensis and Gossypium hirsutum flowers in southeast Queensland. Aggregations were seen only on the upper surfaces of corollas but may have occurred on other flower parts, which were hidden from view. Conspecific females entered aggregations and a small proportion of them mated [18% (n = 163), H. rosasinensis; 30% (n = 181), G. hirsutum]. Most females (87 and 72%, respectively) that did not mate in aggregations walked to other flower parts. Behavior was difficult to observe on these parts, but mating was sometimes observed there. The number of females that landed within aggregations on the upper surfaces of both H. rosasinensis and G. hirsutum corollas was highly correlated with the number of males (r = 0.88, r = 0.93, respectively; P < 0.001). Significantly more mating pairs were observed in high-density aggregations (mean ± SE, 1.10 ± 0.22 and 4.44 ± 0.48, respectively) than in low-density aggregations (0.37 ± 0.11 and 1.67 ± 0.29, respectively) (P < 0.05) on flowers of both species. More F. schultzei females were attracted to sticky traps baited with live conspecific males set among flowering Ipomoea indica (mean ± SE, 8.83 ± 0.32) and G. hirsutum (10.90 ± 0.79) plants than to control traps (0.10 ± 0.05 and 0.70 ± 0.25, respectively) (P < 0.05), presumably in response to male-produced pheromones. Significantly more females were attracted to traps with high male densities than to traps with low densities. We found no statistical evidence that aggregation size influenced mating success (proportion males that mated). Mating success, however, should be evaluated with respect to mating on all flower parts and not just the upper surfaces of corollas. The results of this study constitute the first behavioral evidence for an attractant sex pheromone in thrips.     

Sexual dimorphism in relation to swarming and pair formation patterns in leptocerid caddisflies (Trichoptera: Leptoceridae)

North European Leptoceridae (Trichoptera) perform three types of swarming flight patterns: (1) swarming males of Athripsodesand Ceracleafly in horizontal zigzag patterns over the water surface, (2) the Mystacidesspp. perform vertical zigzag movements, and (3) the flight of males of Triaenodes unanimisMcLach. is a mixture of the horizontal and vertical zigzagging. Also three groups of pair formation behavior can be distinguished. In the first group, of Athripsodesand Ceraclea,the females fly into the male swarms, where they are grasped and carried to the riparian vegetation by the flying males with the females hanging upside-down in genitalia coupling. In the second group, a Mystacidesfemale is caught by a male, when approaching a swarm and both use their wings to fly in tandem to the shore where they copulate. In the third group, of Triaenodes bicolor(Curt.) and Oecetis lacustris(Curt.), the males fly searching for females sitting on aquatic plants and when a female is found the male lands and they copulate immediately while clinging to the plant. The different swarming and mating behaviors might have favored selection for three types of sexual dimorphism: (1) longer forewings in males than females in species which fly in copula, (2) larger eyes in males of the vertically zigzagging species, and (3) much smaller males in the group where males search for females sitting on aquatic plants. In the second group approaching females are detected by males before reaching the swarm and in the third group the female almost always mates with the male which is the first to find her. In conclusion, we suggest that females of Athripsodesand Ceracleahave a greater choice among swarming males than do females of Mystacides, T. bicolor,and O. Lacustris.     

The mating chances of small males of the cerambycid beetleTrachyderes mandibularis differ in different environments (Coleoptera: Cerambycidae)

Some males of the cerambycid beetle Trachyderes (Dendrobias) mandibularisgained access to mates by defending a patchily distributed food resource, the fruits of saguaro cactus (Cereus giganteus).Male beetles differed greatly in fighting ability because of extreme variation in body size and a striking dimorphism in mandibular weaponry. As is typical in resource defense mating systems, larger males had an advantage in combat. Major males with their large pincer jaws invariably defeated minor males with small cutting jaws, and larger majors usually defeated smaller majors. However, although minor males were at a competitive disadvantage on saguaro fruits, they did not suffer a great penalty in terms of mating probability. In contrast, minor males have a considerably lower probability of mating at desert broom (Baccharis sarothroides)where sap ooze sites are few in number and effectively monopolized by major males (Goldsmith, S. K., Behav. Ecol. Sociobiol.20,111–115, 1987). On saguaros, minor males successfully obtained mates through scramble competition while avoiding direct physical competition with larger, territorial major males. Smaller males of either morph may have succeeded in acquiring mates in part because there were many more ripe saguaro fruits than beetles, which made it impossible for larger major males to monopolize females effectively under these conditions.     

Temporal dynamics of mating and predation in mosquito swarms

We determined the numbers of copulations and predatory attacks in swarms ofAnopheles freeborni (Diptera: Culicidae), and the distribution of these events throughout the duration of the swarming period each day. On 19 evenings of observation, we recorded 2724 copulating pairs leaving swarms and 1351 dragonfly (Pantala hymenaea andErythemis collocata) attacks. Mating activity partially coincided with predator activity. Most copulations occurred between 10 and 20 min after the swarms formed, while predation events were most frequent during the initial 15 min of the swarm. We calculated the ratio of copulations to predatory attacks during the swarming period. This ratio was significantly higher in an area sheltered by trees than it was in the open. We suggest that physiological and ecological constraints other than predation operate on the mating system of this anopheline to affect the timing of swarm initiation and swarm site selection.     

Variation in energy reserves and role of body size in the mating system of Anopheles gambiae

Anopheles gambiae mates in flight. Males gather at stationary places at sunset and compete for incoming females. Factors that account for male mating success are not known but are critical for the future of any genetic control strategy. The current study explored variations in nutritional reserves (sugars, glycogen, lipids, and proteins) in wild‐caught swarming and resting males and evaluated the effect of body size and wing symmetry on male mating success. Our results showed that glycogen and sugar reserves are mobilized for flight. Males consume proportionally 5.9‐fold as much energy derived from sugars in swarming activities than when they are at rest. Mated males were on average bigger than unmated ones (P<0.0001). A strong correlation between the left and right wings in both mated and unmated males was found and additional analysis on fluctuating asymmetry did not show any indication of mated males being more symmetrical than unmated ones. The distribution of wing size of mated males was focused around a central value, suggesting that intermediate size of males is advantageous in the An. gambiae mating system. The results are discussed in the context of sexual selection.     

Reproductive behavior of the antLeptothorax (Dichothorax) pergandei

Summary Leptothorax pergandei, the only member of the subgenusDichothorax, is a common ant in Chihuahuan desert habitats in southwestern Arizona. According to colony censuses and relatedness estimates, colonies are mostly monogynous and queens typically mate only once. Mating takes place in local swarming flights; virgin queens attract males with secretions from the poison gland. Some dealate queens running on the soil surface directly after the mating flight had well-developed ovaries containing mature eggs and yellow bodies.     

Widespread 'hilltopping' in Acraea butterflies and the origin of sex-role-reversed swarming in Acraea encedon and A. encedana

In some populations of the butterflies Acraea encedon and A. encedana, most females are infected with a bacterium that kills their sons. The resulting shortage of males is associated with females adopting a sex‐role‐reversed mating system, in which females swarm at landmarks such as hilltops and compete for males. We have observed the mating behaviour of Acraea species that are not known to be infected with the male‐killer. In over half of these species, males were found to aggregate on hilltops. It is likely that this behaviour was ancestral to the sex‐role‐reversed swarms of Acraea encedon and A. encedana, and we discuss how the spread of the male‐killing infection may have converted this mating system into sex‐role‐reversed swarming.     

The influence of horn and body size on the reproductive behavior of the horned rainbow scarab beetlePhanaeus difformis (Coleoptera: scarabaeidae)

The reproductive behavior of horned rainbow scarab beetles,Phanaeus difformis, was studied to determine the influence of morphological traits on intersexual and intrasexual interactions.Phanaeus difformis is a sexually dimorphic dung beetle in which males possess much larger horns than females, and males can be grouped into major and minor male morph categories based on horn size. Male-female pairs cooperated in nest construction and provisioning. In the laboratory, males of both morphs assisted females and were equally successful at copulating. However, in the field larger individuals had a pairing advantage due to greater success in intrasexual competition. Some males used an alternative mating tactic which involved sneaking copulations with paired females. In most cases the sneak male was smaller than the paired male.     

Male Mating Success in the Mountain Dusky Salamander,Desmognathus ochrophaeus: Are Small,Young, Inexperienced Males at a Disadvantage?

Young, small, sexually-inexperienced males suffer lower mating success than older, larger, more experienced males in many species of animals. I compared the mating success of male Desmognathus ochrophaeus (Amphibia: Caudata: Plethodontidae) reared to maturity in the laboratory with that of males collected as adults in the field. Courtship trials were staged in the laboratory between single males and females. Laboratory-reared males were significantly smaller in body size than adult males collected in the field, were certainly inexperienced sexually and were probably younger. No difference was found between laboratory-reared males and field-collected males in any measure of mating success, although the former apparently produced smaller sperm masses. I conclude that newly-mature male D. ochrophaeus are not discriminated against by females in the context of mate choice, and do not need to “rehearse” courtship in order to obtain successful inseminations. However, newly-mature males are probably at a disadvantage in terms of aggressive and sperm competition with larger males.     

Size Assortative Mating and Reproductive Success of the Funnel-Web Spider, Agelena limbata (Araneae; Agelenidae)

Field observations and laboratory experiments were conducted to assess the relation between male size and reproductive success in the funnel-web spider, Agelena limbata Thorell (Agelenidae), in 2 years. In this species, the body size of males is similar to that of females. In the field, size assortative mating occurred in both years. In 1 year, partial correlation coefficient analysis indicates that male cephalothorax width is a beter predictor of the copulated female cephalothorax width than of the date of pairing. In laboratory experiments, females tended to reject courting males that were smaller in relative body size, and males that were larger in relative body size had greater copulation success. Consequently female rejection of smaller courting males has some contribution to size assortative mating. Since larger females deposited more numerous eggs in the field, larger males are expected to have a higher reproductive success.     

Genetic structure in a swarming brown long-eared bat (<Emphasis Type="Italic">Plecotus auritus</Emphasis>) population: evidence for mating at swarming sites

Plecotus auritus, a small, gleaning bat species, lives in small, isolated summer colonies in which both males and females show a high degree of natal philopatry. Despite this, colonies have high gene diversities and low inbreeding coefficients. It has been suggested that inbreeding is avoided because mating occurs during autumnal and spring swarming at hibernation sites. We tested this hypothesis by comparing microsatellite profiles, based on eight loci, of bats from six summer colonies and two swarming sites they were known to visit from radiotelemetry studies. We found high gene diversities (H _s = 0.77) at both swarming sites and summer colonies which were not statistically different. There was no detectable isolation by distance and F_ST was low (0.001). Together, these results suggest high gene flow between sites. Despite this, there was small but significant genetic differentiation amongst summer colonies and between summer colonies and the primary swarming site. We suggest that swarming is important for gene flow and for maintaining genetic diversity in this highly philopatric species and discuss possible reasons for the genetic differentiation observed. The identification and protection of swarming sites should be a major conservation priority for this and other temperate bat species.     

The More the Merrier: Swarming as an Antipredator Strategy in the Mysid <Emphasis Type="Italic">Neomysis Integer</Emphasis>

The swarming behaviour of a Baltic littoral mysid shrimp, Neomysis integer, was studied both in the presence and absence of a predator (European perch, Perca fluviatilis L.). I performed two kinds of laboratory experiments. First, the swarming tendency of mysids and the effect of swarm size on swarm choice were studied. Second, the ingestion rate of mysids was measured when feeding alone versus in a swarm. The results indicate that N. integer actively join swarms. The avoidance of the perch by N. integer individuals was stronger when there was a swarm present. Larger swarms were preferred over smaller ones regardless of presence or absence of the predator. The overall feeding rate was similar when feeding alone and in swarm, but predator cues reduced feeding rate only when the mysids were feeding alone. This study demonstrates the capability of N. integer to assess predation risk and social context and alter their behaviour accordingly.     

The effect of male size on receptivity in femaleLucilia cuprina (Diptera: Calliphoridae)

The first five matings by both large and small L. cuprinamales switched off receptivity in over 90% of females for 7 days after their initial mating. Small males were virtually unable to switch off females after five matings, whereas the fifth to tenth matings by large males rendered nearly two-thirds of females unreceptive. Mating duration of large and small males was about 11 min even after numerous matings. Given the rarity of field virgins and the temporal and spatial variability of female-required resources, larger males may enjoy greater mating success due to their ability to switch off many females in succession. Virgin males preferred to mate with nonvirgin females larger than themselves; males paired with females smaller than themselves adopted mate-rejection behavior typical of unreceptive females.     

Male morphology,performance and female mate choice of a swarming insect

1. Females of many species select mates based on important morphological and performance traits. This behaviour likely facilitates reproductive success thus exhibiting sexual selection. Most such studies have evaluated a single morphological variable, and only a minority of them studies the effects of behaviour and performance (functional capacity: Irschick et al., Evolutionary Ecology Research, 10 , 177–196, 2008) at all.
2. This study compares male morphological and performance traits differing in three variables that may correlate with fitness: condition index, flight ascent speed and resistance to torpor in relation to male mating success in the parasitoid wasp species Alabagrus texanus (Braconidae), a species where males swarm about emerging virgin females that display both choosy and non-choosy behavioural phenotypes.
3. Males that successfully mated with choosy females exhibited higher condition indices and somewhat stronger resistance to torpor than other males. Conversely, males that mated with non-choosy females did not differ in any trait from other males we measured. Early-arriving males did not have higher condition indices or greater mating success than other males.
4. Thus, both morphological and performance traits contributed to male success, which acted through female choice, indicating a role for sexual selection. Patterns of choice further differed among females, independent of male traits.