Site-specific mate-finding strategies and oviposition behavior inCrocothemis erythraea (Brullé) (Odonata: Libellulidae)

Mate-finding strategies and adaptations in pre- and postcopulatory behaviors to avoid male disturbance were studied in Crocothemis erythraea at two different sites. At ponds without perch sites males patrolled with temporal partitioning of the limited oviposition sites and male-male disputes were rare. The arrival rate of females was high. At temporary marshes with dense emergent vegetation the oviposition sites were widely distributed. Males mainly perched and interacted with longer disputes. At both types of habitats with high male densities females showed a similar number of copulations per visit and oviposition durations. Postcopulatory behavior to avoid male disturbance and to decrease remating of the female differed in both sexes. At the ponds with patrolling males the probability of remating in guarded and unguarded ovipositions was similar and higher than at the marshes. At the marshes 78% of rematings occurred when the guarding male was still involved in disputes with the previously disturbing male. At the ponds females hovered before escaping successfully from approaching males and they changed to another oviposition site where they continued oviposition. Females at the marshes remated after surprise attacks by neighboring males.     

Mating tactics and male wing dimorphism in the damselfly,Mnais pruinosa costalis selys (Odonata: Calopterygidae)

Males of the damselfly,Mnais pruinosa costalis, exhibit wing color dimorphism: one form has orange wings, and the other hyaline wings which resemble female wings. The former is usually territorial and the latter uses sneaky mate securing tactics. When orange-winged males failed to establish territory, they became floaters that day. Hyaline-winged males perched around their territories and often, formed in tandem without any apparent courtship behavior when they found females. Their copulation frequency was higher and copulation duration longer than those of territorial males. A few females oviposited without remating. Total oviposition duration of females with which a hyaline-winged male mated was more than 32 min per male on average in a day Females that copulated with hyaline-winged males often remated with orange-winged residents before oviposition. Total duration of oviposition bouts of females after mating with floaters was short (15 min), while that with territorial residents was long (66 min). As a result, total oviposition duration of females with which an orange-winged male mated was about 40 min in a day. The reproductive success of the hyaline-winged males may be similar to that of the orange-winged males.     

Female and male interactions during courtship in Calopteryx maculata and C. dimidiata (Odonata: Calopterygidae): Influence of oviposition behaviour

Calopteryx maculata and C. dimidiata damselfly females respond to male courtship with specific displays which signal differences in their receptivity. These include a rejection (wing spreading) and an invitation (wing-flipping) display, as well as a neutral (sit still) response. There are interspecific differences in the likelihood of each female display and in male responses to these displays. C. maculata males persist in courtship irrespective of female response, while C. dimidiata males generally stop courting when the female's response is rejection or neutrality. I suggest that these differences result from interspecific differences in oviposition behaviour. Female C. maculata oviposit at the water surface, which exposes them to disturbance by males attempting to mate. Females are therefore likely to remate to secure postcopulatory guarding when changing oviposition sites and males are expected to be persistent in courtship. Female C. dimidiata submerge to oviposit, which frees them from male disturbance and means that males have less control over female access to oviposition sites. Males therefore have less influence on mating by females and are expected not to persist in courtship of non-receptive females.     

Repeated copulations benefit of the female inLethocerus deyrollei vuillefroy (Heteroptera: Belostomatidae)

TheLethocerus deyrollei male copulates repeatedly with the same female before and between ovipositions. Females stopped oviposition and waited for the next copulation when males were experimentally removed. This result suggests that females need to copulate before each oviposition bout. Since eggs fail to hatch without care of males, females have to detain males until the end of sequential ovipositions. Males assure their paternity with repeated copulations, and females can thus detain males.     

Mating behavior and the evolutionary significance of mate guarding in three species of crane flies (Diptera: Tipulidae)

Three species of crane flies-Dactylolabis montana, Limonia simulans,and Antocha saxicola-gather near streams to mate and oviposit. All species are polygamous and sex ratios at these sites are male-biased. After a short mating bout, males guard females by standing over them during oviposition. Sperm competition appears to be intense and to follow last-male advantage, based on the packing of sperm within the two elongate spermathecae. Males of A. saxicolasuccessfully defend against rivals over 85% of the time. In contrast, defending males of D. montanaand L. simulanslose the female over 65% of the time during interactions with rivals. Despite the high frequency of loss, defending males gain additional oviposition time by engaging rivals in combat while the female continues to oviposit. Thus, a guarding male does not have to retain the female for guarding to be adaptive. Legs and claws of all species are sexually dimorphic and play an important role in guarding and defending.     

Male perch selection and the mating system of the robber fly,Promachus albifacies (Diptera: Asilidae)

We studied the activity and spatial distribution of the robber fly,Promachus albifacies, in a desert grassland habitat in central New Mexico. Late in the season males spent most of the daytime on or near cholla and yucca plants that had dead stems or dead flower stalks at least 1 m high. Of the three hypotheses (thermoregulation, foraging, mate encounter site) considered as explanations for this distribution, the mate-encounter-site hypothesis was best supported. Plants used by females as oviposition sites were the focus of male activity. Males perched within or near these plants and attempted copulations with females detected nearby. Most matings were initiated at these locations. Seasonal changes in male and female activity also supported the mate-encounter-site hypothesis. Early in the season, females spent little time ovipositing, and predictably, males spent little time on or near these plants. Such a mating system may be described as resource defense polygyny, since males acted aggressively toward one another at oviposition sites even when females were not present. However, the short tenure of males at these sites is suggestive of scramble competition polygyny. We discuss possible reasons why this particular mating system has evolved.     

Function and genetics of long versus short copulations in the cactophilic fruit fly,drosophila mojavensis (diptera: drosophilidae)

Variation in copulation duration of Drosophila mojavensisstrains was influenced by both sexes. Males maintained predominant control, as copulation duration of pairs from different strains was more similar to that of the strain from which the male was derived, but female origin also contributed significantly to the duration of copulation. Variation among strains was controlled by genes acting additively in both sexes. The size of both males and females also affected copulation duration. Small males copulated longer on average than large males, while males paired with large females copulated longer than those paired with small females. The importance of copulation duration to fitness was tested by correlation analyses with male size, female size, female remating latency, and number of eggs laid prior to female remating. Longer copulations stimulated earlier oviposition, possibly by increasing accessory gland secretions that are passed by males during copulation.     

Alternative mate-finding tactics in a non-territorial damselfly (Odonata: Coenagrionidae)

Males of the non-territorial damselfly Enallagma hageni have two alternative tactics for finding mates: (1) they search the banks of the pond for unmated females (searching tactic), or (2) wait at oviposition sites for females that resurface prematurely from underwater oviposition (waiting tactic). Although the searching tactic yielded more fertilizations than the waiting tactic, for time invested, the waiting tactic became increasingly successful later in the reproductive season due to changes in female oviposition behaviour. The two tactics can be maintained in the population because males can mate by the waiting tactic during the afternoon when few females are available to searchers. Among males visiting the breeding site an equal number of times, males mating by a mixture of tactics were as successful as males mating only by the main tactic. Because marked males were found to use both tactics, these behaviours are interpreted as evidence of behavioural plasticity within individuals, representing one conditional evolutionary strategy.     

Confirmation of the existence of alloparasitoids in nature – host relationships of an Australian Coccophagus species that parasitizes mealy bugs

Heteronomous hyperparasitoids are parasitic wasps with sex‐related host relationships that are unique to a group of genera in the chalcidoid family Aphelinidae. Females are primary parasitoids of various sedentary bugs (mainly, scale insects, mealy bugs, and whiteflies). Males, in contrast, are hyperparasitic, and they frequently develop at the expense of female conspecifics. Alloparasitoids constitute a special category of heteronomous hyperparasitoids, for their males never develop through female conspecifics. The existence of alloparasitic host relationships and the utility of the category ‘alloparasitoid’ have both been questioned. Here, we present results that confirm the existence of the alloparasitic way of life among heteronomous aphelinids. We investigated an undescribed species of Coccophagus (Hymenoptera: Aphelinidae), an Australian parasitoid that attacks the introduced lantana mealy bug, Phenacoccus parvus Morrison (Homoptera: Pseudococcidae), in Queensland. A year‐long field survey regularly returned large numbers of female Coccophagus spec. near gurneyi individuals from P. parvus (total n = 4212), but only few males (n = 11). Males emerged from samples only when the encyrtid parasitoid Anagyrus diversicornis (Howard) (Hymenoptera: Encyrtidae) was present in samples in relatively high numbers. Laboratory oviposition tests confirmed that A. diversicornis is a male host and showed that males do not develop at the expense of conspecific females. Other studies show that males are attracted in numbers to virgin females held in cages above mealy bug‐infested Lantana montevidensis (Spreng.) Briq. (Verbenaceae) in the field, demonstrating that they are common in the population as a whole. This confirms that the males need hosts other than conspecific females and that their usual hosts are present outside of the lantana/P. parvus system. The implications of these results for developing a realistic classification of heteronomous host relationships are discussed.     

Mating Behavior of Cephalonomia tarsalis (Ashmead) (Hymenoptera: Bethylidae) and the Effect of Female Mating Frequency on Offspring Production

The courtship behavior of Cephalonomia tarsalis, a solitary semiectoparasitoid of Oryzaephilus surinamensis, was investigated in the laboratory. Courtship behavior includes a series of stereotypic movements. Males play the most active role, executing the majority of courtship action, and females respond with relatively limited observable behaviors. Males typically keep antennae still during encounters with females prior to mounting, which may be correlated with recognition of the female's sexual status. After mounting, males display a series of movements on females, such as antennae touching female's antennae, antennae or mouth touching female's head or thorax, and walking around on female, which may serve to stimulate females towards increased receptivity. Females signal receptivity by assuming a stereotypical posture of remaining stationary, with head down, and antennae still in front of the body. The male then inserts his aedeagus and the pair copulates. After an average of 40.4 s of copulation, females signal the end of copulation by waving the antennae and moving away from the copulation site. Males continue copulating for a short time after females start moving but dismount soon thereafter. After dismounting, the two wasps move away from each other immediately, and they typically begin grooming. Neither males nor females exhibit mating preference based on mate's mating status in both choice and no-choice tests. The male is polygynous and the mated female can mate multiple times within the first 3 days after starting oviposition. However, female mating frequency does not affect the production of female progeny.     

Copulation Is Not a Prerequisite to Male Reception of Eggs in the Golden Egg Bug Phyllomorpha laciniata (Coreidae; Heteroptera)

Females of the golden egg bug, Phyllomorpha laciniata, lay eggs on the backs of conspecifics. Male response to female oviposition attempts is either passive or resistant. Passive males remain still during oviposition, while resistant males move repeatedly and thereby delay or avoid being encumbered. We investigated how previous mating experience affected male acceptance of eggs. Males from two Spanish populations, from Andalusia and Catalonia, were allowed to mate with single females repeatedly. These experimental pairs were then presented with either a single, nonmating male or a pair in copula. We expected mating partners to resist oviposition attempts less strongly than nonmating males but no differences were detected. However, there was a significant difference in behavior exhibited by males from the two populations; males from Catalonia were relatively passive but males from Andalusia routinely resisted encumbrance. Predation pressure and the availability of receptive females may explain the observed differences between the populations.     

Flight movement of Scapanes australis australis (Boisduval) (Coleoptera: Scarabaeidae: Dynastinae) in Papua New Guinea: a radiotelemetry study

Abstract We used radiotelemetry and/or chemical light-tags to track the flight of 15 individuals of Scapanes australis in Madang Province, Papua New Guinea. This species causes severe economic impacts on coconut palms in young plantations. Flights to feeding, mating, resting, and possibly oviposition sites covered distances of 52 to 835 m in males, and from 245 m to>1000 m in females. Upon release, females flew in a tight upward spiral above canopy level (>20 m), then usually flew along a single bearing out of radio reception within 1 min of initiating flight. Dispersing females probably follow scent trails to pheromone-releasing males that occupy feeding galleries excavated most frequently in coconut palms, or search for oviposition sites. Most tagged females were not found again, because they dispersed beyond the tracking capabilities of our radio-receivers, but one female was followed for 245 m to a feeding gallery excavated by an adult male. Males typically flew within 5 m of the ground, took erratic flight paths with numerous turns, and frequently circled coconuts and other host plants. We followed males from the release point until they ceased flight for a night. Males passed daylight hours either in a feeding gallery within a host plant or under soil litter.     

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.     

Hilltopping in the Pipevine Swallowtail Butterfly (Battus philenor)

In central Arizona, receptive females of the pipevine swallowtail, Battus philenor, are widely scattered in time and space, and in this region the butterfly's mating system is one in which males patrol mountain peaks. Hilltopping males engage intruding males in ascending flights that appear to be ritualized aerial combat with individuals defending patrolling sites for relatively short periods on any given day. The day-to-day appearance of marked males is irregular, unlike the site fidelity shown by males of many other hilltopping insects. The distinctive pattern of male territoriality in B. philenor may be partly a response to very low male and female density in the observed population. Males at the hilltop chase, court, and attempt to copulate with virgin females released near them. Males assess the receptivity of females rapidly, and receptive females permit a lengthy copulation to occur after a courtship that lasts less than 30 s. During an initial copulation males pass a spermatophore that weighs about 6% of their body mass, with partners on following days receiving a smaller but still substantial donation.     

The effect of differences in body size on the male territorial system of the fly Dryomyza anilis

Drymyza anilis nales defend carcasses, the oviposition sites for females. On carcasses less than 100 g in weight, a single male establishes a teriitory. Ther sex ratio at carcasses is male-biased. Territorial males are larger than other males on average, and move and attack other males more frequently than non-territorial males do. Large carcasses attract more males than smaller ones, but the female, but the advantage of territorial behaviour decreases with increasing density of males. Copulating males are significantly larger than average males, but smaller than territorial males, suggesting than some non-territorial males have access to females. Males seem to be albe to assess a female's egg load, and to adjust the duration of copulation accordingly.     

Growth and survivorship as proximate causes of sexual size dimorphism in peninsula dragon lizards Ctenophorus fionni

Males and females differ in body size in many animals, but the direction and extent of this sexual size dimorphism (SSD) varies widely. Males are larger than females in most lizards of the iguanian clade, which includes dragon lizards (Agamidae). I tested whether the male larger pattern of SSD in the peninsula dragon lizard, Ctenophorus fionni, is a result of sexual selection for large male size or relatively higher mortality among females. Data on growth and survivorship were collected from wild lizards during 1991–1994. The likelihood of differential predation between males and females was assessed by exposing pairs of male and female lizards to a predator in captivity, and by comparing the frequency of tail damage in wild‐caught males and females. Male and female C. fionni grew at the same rate, but males grew for longer than females and reached a larger asymptotic size (87 mm vs. 78 mm). Large males were under‐represented in the population because they suffered higher mortality than females. Predation may account for some of this male‐biased mortality. The male‐biased SSD in C. fionni resulted from differences in growth pattern between the sexes. The male‐biased SSD was not the result of proximate factors reducing female body size. Indeed SSD in this species remained male‐biased despite high mortality among large males. SSD in C. fionni is consistent with the ultimate explanation of sexual selection for large body size in males.     

Female mate choice through spawning parade formed by male-male competition in filefishRudarius ercodes

In the small filefishRudarius ercodes inhabiting temperatre seaweed beds, 2–10 males follow a gravid female, in a line until spawning early in the morning. Formation of the spawning parade and change of male order were investigated in a large aquarium. Males competed for the position nearest to the female during the parade, while the female controlled the parade by her swimming speed and course. During the parade, male members and their order changed frequently. The male order in the parade was related with the intensity of nuptial coloration, which changed according to the social rank. The female sometimes tried to take a spawning posture but rejected spawning when male positioning was not good for her, for example, far different from parading order. The female spawned with 2–5 males on each side. The nearest mating positions to the female were usually occupied by two males that had been staying at an anterior position in the parade for a long time. During the spawning parade over a long distance and time, females ofR. ercodes can choose multiple suitable males in a variable environment like a temperate seaweed bed.     

Male mating preference for female survivorship in the seaweed fly Gluma musgravei (Diptera: Coelopidae).

The seaweed fly mating system is characterized by pre-mating struggles during which females exhibit a mate rejection response involving kicking, shaking and abdominal curling. Males must resist rejection until females become passive and allow copulation to take place. However, despite the vigorous nature of the struggle males frequently dismount passive females without attempting copulation. Here we show that rejected females suffered higher post-encounter mortality rates than those accepted by males in the seaweed fly Gluma musgravei. Furthermore, we show that males also preferentially mounted females with higher future longevity. We propose that this male mate choice for female survivorship has evolved as a result of females often having to survive for long periods after mating until suitable oviposition sites become available. Such male preferences for female survivorship may be common in species in which oviposition must sometimes be substantially delayed after mating.     

Social Network Analysis of Male Dominance in the Paper Wasp Mischocyttarus mastigophorus (Hymenoptera: Vespidae)

Social aggression is a pervasive feature of insect societies. In eusocial Hymenoptera, aggression among females can affect task performance and competition over direct reproduction (egg laying); in most species males participate in social interactions relatively rarely. Males of the independent-founding paper wasp Mischocyttarus mastigophorus are exceptional: they are aggressive toward female nestmates, leading us to explore the function of this unusual behavior. We applied social network analyses to data on M. mastigophorus social aggression to quantify sex differences in giving and receiving social aggression. The network analyses supported the pattern of biased male aggression toward female nestmates; females are relatively rarely aggressive to males. We then asked whether male aggression toward females was biased by females’ relative ovary development. Males were more aggressive toward females with better-developed ovaries, opposite to patterns of aggression among females. Because food brought to the colonies is often monopolized by dominant females, we suggest that males direct aggression toward socially dominant females with better-developed ovaries to obtain food. The implications of biased male aggression for female task performance and physiology are unknown.

     

Females prefer mating males in the carmine triplefin,Axoclinus carminalis,a paternal brood-guarder

Synopsis This study investigates the role of male mating status in female choice patterns in the carmine triplefin, Axoclinus carminalis, a tripterygiid fish that exhibits paternal care. The distribution of daily reproductive activity is clumped, with many males receiving no mates and some receiving three or more. Females in this species do not prefer larger males, and characteristics of the oviposition site appear to have minimal effects on male mating success. When a female is removed from a male early in the daily spawning period, that male attracts fewer additional females for the remainder of the spawning period than does a control male. These changes in mating success are temporary, and do not affect mating success on subsequent days. A preference for mating males or males that are guarding eggs could provide asymmetric benefits for males to defend oviposition sites. This preference for males with eggs could be acting alone or with other factors such as high variance in oviposition site quality to favor the evolution of paternal care in fishes.