The possibility of sex and nymph discrimination by the male cockroach,Nauphoeta cinerea

The possibility of sex and nymph discrimination by males was investigated in the cockroach,Nauphoeta cinerea (Olivier). A sexually mature male takes a courting position toward a sexually mature female when he comes into contact with her and recognizes her through antennal contact. In contrast, males often behave aggressively toward each other: they bite at each others; wings and/or legs, chase each other and antennate mutually. The male, however, does not show conspicuous behavior (mating behavior or aggressive behavior) toward nearby nymphs. The male produces audible sounds when he courts a sexually mature but non-receptive female who does not respond to his courtship behavior. We found that the male also stridulates after he repeatedly courts immature teneral females, males and (last-instar) nymphs. After the bodies of teneral insects are sclerotized, the male shows courship and stridulation behavior toward sexually mature but non-receptive females but not toward mature males and nymphs. At this stage the male begins to behave aggressively toward other post-teneral mature males. We think that the variability of the sexually mature male's behavior toward other conspecifics (courtship behavior toward female, aggressive behavior toward male and no conspicuous response toward nymph) results from the male's recognition of adult and nymph.     

Epigamic display and unique mating position inWyeomyia arthrostigma (Diptera: Culicidae)

The mating behavior ofWyeomyia arthrostigma is more complex than that reported forW. smithii. Like some other genera in the tribe Sabethini, flyingW. arthrostigma males approach females perching on vertical sticks. A male aligns himself next to a female by seizing her wing and flipping sideways to land next to her, rather than beneath her. He then performs a series of abdominal bobbing movements, the pair achieves superficial genital coupling while the male's proboscis rotates and snaps down, and the antennae spread farther apart. Finally, the pair shifts to full copulation, and in this phase insemination occurs. In the copulatory position the abdomens of male and female are almost at right angles to each other, made possible by a twisting of the male's terminal segments. The nature of the mating process and its similarity to some elements ofSabethes andTopomyia mating indicate that males may be performing a courtship display.     

Courtship behavior of the mosquitoSabethes cyaneus (Diptera: Culicidae)

Unlike any other mosquito reported, Sabethes cyaneus(Fabricius) displays an elaborate courtship before and during copulation. A male approaches a female suspended from a horizontal stick, suspends himself in front of her as he grasps her folded wings, and proceeds with a series of discrete stereotyped behaviors that involve proboscis vibration and movement of iridescent blue paddles on his midlegs. The sequence of these behaviors is as follows: freeleg waving, swinging, copulation attempt, superficial coupling, waving, genital shift, waggling, and release. Insemination occurs after genital shift. The only overt reciprocation by the female is abdomen lowering during the male's swinging. Courtship is often unsuccessful, and males are usually rejected during freeleg waving. The relation between male performance and mating success remains obscure.     

Courtship Behavior and Detection of Female Receptivity in the Parasitoid Wasp Urolepis rufipes

Once a Urolepis rufipes male mounted, the female beat her antennae against his mouth and clypeus. Immediately after he swept his antennae rapidly downward and extruded his mouthparts, her abdomen rose as she opened her genital orifice. Almost simultaneously he backed up for copulation and she folded her antennae against her head. Neither her abdomen rising nor her antennal folding were essential to his backing up as determined from their timing and from experiments in which her abdomen was sealed or her antennae were removed. Females did not open their genital orifice if with a sealed-mouth male; and antennae-removed females did not open even in the few cases where untreated males extruded their mouthparts. Unlike a closely related species, females mounted by sealed-mouth males did not open in response to air from containers of mating pairs.     

Resource attractiveness of the male beaugregory damselfish and his decision to court or defend

We examined the decisions territorial male beaugregory damselfish (Stegastes leucostictus) make when presented with mating and aggressive situations simultaneously. Specifically, we testedhow males responded to simultaneous and consecutive presentationsof conspecific males and females in bottles. We hypothesizedthat (1) territorial males would show lower levels of courtshiptoward females when a competing male is also present comparedto when only the female is present and (2) territorial maleswould show higher levels of aggression toward intruding maleswhen a female is also present on their territories than whenonly the intruder is present. We predicted that males withhigh-quality breeding sites would court females and attackcompetitors more vigorously than males with low-quality breedingsites. Males on low-quality breeding sites exhibited fewerconspicuous courtship displays toward bottled females and alower bite rate toward bottled males than did the males onhigh-quality breeding sites. We concluded that poor breeding-sitequality was responsible for the decline in the most conspicuous aspects of both courtship and aggression. When presented simultaneouslywith a bottled male and a bottled female, defenders of bothbreeding-site types drastically reduced the number of courtshipdisplays and the amount of time they spent near the female.Thus, all aspects of courtship were reduced in the presenceof a male intruder. Time spent near the bottled male also decreased in these simultaneous presentations; however, this decreasewas less dramatic than the reduction in time spent near bottledfemales. Habitat quality did not affect these trade-off decisions,but the bite rate exhibited toward the bottled male increasedin the simultaneous presentations compared to the single presentations.Due to this increase in a territorial male's defensive behaviorwhen a female is present, we conclude that the presence of afemale temporarily increased the value of a territory. We suggestthat the possible loss of a territory to an intruding maletakes priority over the potential benefits of successfullycourting a single female and that it is a male's future reproduction,as well as his current reproduction, by which he assesses hisbenefits.     

Sperm transfer and mating in Ricinoides hanseni (Ricinulei: Arachnida)

Ricinuleid reproduction involves indirect sperm transfer using the highly modified distal podomeres of the third legs of the male. This is homologous with the apparatus and technique used by male spiders, which possess elaborate pedipalps. The interpretation of the method of sperm transfer is based upon morphological studies of the male's third legs and the female's genital atrium and the behaviour of males during mating. The male charges the emboli of his modified leg tarsi with sperm from his penis. After climbing on to the back of a receptive female he delicately and precisely places a modified tarsus in the genital atrium of the female. A series of lobes on the tip of part of the modified tarsus fit into a number of vesicular evaginations of the female's genital atrium. The lobes form part of the mechanism which provides a firm attachment of the male's tarsal elements with the female's genital atrium during sperm transfer. A tubular element of the modified tarsus fits into a spermatheca of the female. Sperm and seminal fluid are then injected from the male's embolus into the female's spermatheca.     

Differences between the sexes in direction and duration of response to seeing a potential sex partner mate with another

We have shown previously that: (1) female Japanese quail, Coturnix japonica, increase and male Japanese quail decrease their tendencies to affiliate with potential sex partners after seeing them mate, and (2) in both sexes of quail, affiliative preferences and choice of a sex partner are highly correlated. Here we predict that because effects of a prior male's sperm on a second male's probability of fertilizing a female are relatively brief, a male's avoidance of whichever member of a pair of females he has seen mating should be transitory. Conversely, because female quail seek high-quality males as mates and quality is a relatively permanent characteristic, females' preferences between males should remain constant over time. We found, as predicted, that the durations of effects on affiliation of seeing a potential sex partner mate differed in male and female quail. Forty-eight hours after male quail saw a female mate, they no longer avoided her, whereas 48 h after female quail saw a male mate, his attractiveness remained enhanced. We conclude by suggesting that both the direction and the duration of responses of male and female Japanese quail to seeing a member of the other sex mating enhance the fitness of members of each sex. Copyright 2000 The Association for the Study of Animal Behaviour.     

Courtship song, male agonistic encounters, and female mate choice in the house cricket,Acheta domesticus (Orthoptera: Gryllidae)

Whether female crickets choose among males based on characteristics of the courtship song is uncertain, but in many species, males not producing courtship song do not mate. In the house cricket,Acheta domesticus, we examined whether a female chose or rejected a male based on his size, latency to chirp, latency to produce courtship song, or rate of the high-frequency pulse of courtship song (“court rate”). We confirmed that females mated only with males that produced courtship song, but we found no evidence that the other factors we measured affected a female’s decision to mate. In addition, we investigated whether the outcome of male agonistic encounters affected the subsequent production of courtship song. In one experiment, we observed courtship and mating behavior when a single female was placed with a pair of males following a 10-min interaction period between the two males. Winners of male agonistic encounters had higher mating success. However, winners and losers of agonistic encounters were not different in their likelihood or latency to produce courtship song or in the number of times they were disrupted by the other male in the pair. In a second experiment, we allowed two males to interact for a 10-min period, but following this interaction period, we placed a female with each male separately and observed courtship and mating behavior. The mating success of winners and losers was not different under these circumstances, and we found no differences between winners and losers in any subsequent courtship or mating behavior examined. We conclude that winning agonistic encounters influences a male’s mating success in ways other than his production of courtship song and this effect is lost when winning and losing males are separated and each is given an opportunity to mate.     

Mating behavior of Pine Sawyer,Monochamus saltuarius Gebler (Coleoptera: Cerambycidae)

Mating behavior of the pine sawyer, Monochamus saltuarius Gebier (Cerambycidae: Lamiinae) was observed on pine trees in an outdoor net cage kept in one healthy pine tree and a cluster of pinelogs (cut over one month) to attract the beetles. When sawyer adult pairs released into net cage, they all moved to the pinelogs. And then the male was staying motionless with his antenna outstretched while the female was actively moving in his vicinity. The mating behavioral reactions were followed by the next steps: The first phase of courtship was initiated by the female approach toward the male. Second, male dashed, contacted antenna and mounted female's back. Third, female carried the male on her back and walked around and then male began to lick. Fourth, male inserted his penis into the female's genitalia when female stopped walking. While a long pairbond, the mating pair repeated copulations, lastly, when mating is over, male and female stayed separately. The mating began on sunset and resting of both male and female began at the temperature below about 20 °C. Substantially straightforward mate searching by female indicates the presence of a male sex pheromone.     

Sexual coercion does not exclude luring behavior in the climbing camel-spider <Emphasis Type="Italic">Oltacola chacoensis</Emphasis> (Arachnida,Solifugae, Ammotrechidae)

Sexual coercion in the form of forced copulation has been used as a typical example to illustrate the conflict of interests between females and males. Among arthropods, forced copulation has been reported for some groups of insects and crustaceans, but not for arachnids. In the present work, we analyse and describe the behavioral patterns of mating behavior of the climbing camel-spider, Oltacola chacoensis, relating it to relevant morphological features, In this species, the male forcefully clasps the female’s genital region with his chelicerae and locks her fourth pair of legs with his pedipalps. In some cases, the cuticle of the female’s abdomen was damaged by this cheliceral clasping. In contrast to other camel-spiders, the female O. chacoensis never remained motionless during mating, but continuously shook her body, opening her chelicerae notably towards the male. Despite this coercive context, males performed copulatory courtship (tapping with pedipalps) and females showed an apparent cooperative behavior (they remained still during a short period of the sperm transfer phase). These results strengthen the idea that sexual coercion (in the form of forced copulation) and luring behavior (in the form of copulatory courtship) are not two mutually-exclusive male’s strategies during a single copulation.     

Males mate guard in absentia through extended effects of postcopulatory courtship in the parasitoid wasp Spalangia endius (Hymenoptera: Pteromalidae)

The proximal mechanisms leading to monandry have been little studied in most insect orders, including Hymenoptera. In the parasitoid wasp Spalangia endius, mated females are less attractive (less often mounted) than virgins and are unreceptive (unlikely to allow copulation). Which aspects of mating are responsible was tested by observing male responses toward females whose mating had been interrupted at various stages. All females were allowed to receive precopulatory courtship and to open their genital aperture to copulate. Then some were interrupted before copulation, some after copulation but before postcopulatory courtship, and some were allowed to complete postcopulatory courtship. Females that had copulated were not less attractive than females that had not. In contrast, females that had received postcopulatory courtship were clearly both less attractive and less receptive. Thus, postcopulatory courtship functions as extended mate guarding, by making the female less attractive and less receptive to subsequent males even after the original male is no longer present. The effect of postcopulatory courtship on female attractiveness was persistent but imperfect: when males were presented sequentially to mated females, most but not all males retreated without mounting, and a female could repulse more than twenty males in succession.     

Seizing the Opportunity: Subordinate Male Fowl Respond Rapidly to Variation in Social Context

Dominance affects mating and reproductive success in many group-living species. Potential mechanisms include subordinates being inherently less attractive and social constraints imposed by dominant individuals. To test the former possibility, we measured morphology in 45 male fowl, Gallus gallus , prior to group formation. Males were then assigned to social groups (three males and three females in each). None of the measured traits predicted subsequent social status, suggesting that subordinates were not inherently unattractive. We then manipulated social constraints in each group to test if subordinates were socially constrained. We removed either the alpha (experimental) or the gamma male (control) for 40 min and observed the effect on the beta male's reproductive behavior. Controls accounted for putative group size and disturbance effects, and ensured that the only difference between treatments was the relative dominance of the remaining male. In each trial, we measured the beta male's courtship effort and his mating success, as well as his proximity to females and to the remaining male. Results show that social context did not affect mating success, but had a significant impact on courtship behavior. Beta males courted significantly more often when they had exclusive access to a female, as opposed to when another male was nearby. Furthermore, their courtship effort was higher if the nearby male was a fellow subordinate, as opposed to the dominant male. We conclude that both the proximity and social status of nearby males affects, either directly or indirectly, the courtship efforts of subordinate male fowl.     

Virgin male mating advantage in a primitive acoustic insect (Orthoptera: Haglidae)

Male reproductive behavior in the relict flightless haglid, Cyphoderris strepitans,entails the generation of sound signals and the provision of nuptial gifts to mates. These food gifts take two forms: (1) a gelatinous mass (spermatophylax) augmenting the spermatophore and (2) fleshy metathoracic wings adapted to be eaten. The female consumes a portion of the male's underwings during courtship and copulation and the spermatophylax afterward. The incidence of wing-feeding wounds can be used to monitor the mating success of field-caught males. If, when a male mates, he compromises his ability to provide subsequent nutritive gifts, females would benefit by mating with virgin rather than nonvirgin males. To test this, mating success of virgin and nonvirgin males was compared in a field population. Virgins were found to obtain more matings than explained by their numbers relative to nonvirgins in the population. We conclude that, having mated, a male is at a disadvantage, relative to his virgin competitors, in securing further matings.     

The Effect of Limb Loss on the Courtship and Mating Behavior of the Wolf Spider Pardosa milvina (Araneae: Lycosidae)

Limb loss is common in the wolf spider Pardosa milvina, appearing in nearly one third of adult males but occurring less frequently among adult females and juveniles. Since males wave their first pair of legs during courtship displays, the reproductive consequences of limb loss may be significant. We measured the courtship and mating effects of the loss of one, two, or four legs among adult male P. milvina. Missing one or two legs did not significantly reduce a male's ability to mate, but missing four legs was detrimental to mating success, reduced both courtship intensity and copulation duration, and increased cannibalism frequency. Results suggest behavioral flexibility in compensating for limited leg loss and a defensive function of the anteriormost legs to thwart female cannibalism attempts.     

Duration of courtship effort as a costly signal

We consider a male and a female in a courtship encounter over continuous time. Both parties pay participation costs per unit time. The game ends when either one or other of the parties quits or the female accepts the male as a mate. We assume that there is a binary variable which determines whether the male is a “good” or “bad” type from the female's point of view, according to either his condition or his willingness to care for the young after mating. This variable is not directly observable by the female, but has fitness consequences for her: she gets a positive fitness payoff from mating with a “good” male but a negative fitness payoff from mating with a “bad” male. We assume also that a “good” male has a higher ratio of fitness benefit from mating to fitness cost per unit time of courtship than a “bad” male. We show that, under suitable assumptions, there are evolutionarily stable equilibrium behaviours in which time-extended courtship takes place. A “good” male is willing to court for longer than a “bad” male; in this way the duration of a male's courtship signals his type, and acts as a costly handicap. By not being willing to mate immediately the female achieves a degree of screening because the posterior probability that the male is “good”, conditional on his not having quit the game, increases with the duration of courtship.     

Distastefulness as a defense mechanism in Aplysia brasiliana (Mollusca: Gastropoda)

An unusual courtship pattern for fiddler crabs is described from field observations in Panama. This behavior pattern, referred to here as “directing,” differs considerably from the more frequently observed communal courtship system found in close relatives of Uca deichmanni. A male involved in “directing” approaches a female and attempts to carry or maneuver her into his burrow for mating. The female usually struggles to escape from the male. This activity often attracts other males which attempt to “direct” the female if she escapes from the first male. A male is most successful in “directing” a female into his burrow if a) he is larger than the female, b) the female is wandering (a sign of physiological receptivity) prior to the “directing” attempt, and c) several males attempt to “direct” the female at once. The results suggest that females are choosing mates by inciting several males to compete for them. The males which successfully “direct” the struggling females are probably the most fit males.     

Courtship tactics in garter snakes: how do a male's morphology and behaviour influence his mating success?

The behavioural determinants of male mating success play a pivotal role in sexual selection, but remain poorly known for most kinds of organisms, including most reptiles. In Manitoba, Canada, large numbers of red-sided garter snakes, Thamnophis sirtalis parietalis, court and mate in early spring near communal overwintering dens. To understand how a male's morphology and behaviour might influence his mating success, we videotaped 21 groups of snakes each comprising four males of varying body sizes plus a female. All males engaged in courtship, and mating occurred in all groups. Males with better body condition courted more vigorously and successfully than their smaller rivals did. The males that obtained matings were those that maintained their own cloaca closest to that of the female, aligned most of their body with the female, showed high rates of caudocephalic waving, chin pressing and tail searching, and did not allow other males to insert their body beside the female's. These behavioural differences between ‘winners’ and ‘losers’ were apparent from the beginning of each trial. Thus, male mating success in this ‘scramble’ system is determined not by chaotic, stochastic struggle (as has often been inferred) but instead is strongly linked to male courtship tactics. Energy stores (as evidenced by good body condition) may be critical determinants of mating success in these vigorous courtship episodes.     

The transvestite serpent: why do male garter snakes court (some) other males?

In large mating aggregations of red-sided garter snakes, Thamnophis sirtalis parietalis, in Manitoba, male courtship is directed not only to females, but also to other males with female-like skin lipids ('she-males'). We show that 'she-maleness' is an intrinsic property of a male rather than an artefact of lipid transfer from females, and that male-male courtship is very common in the field. She-males were distinctive in terms of appearance (they were heavier than other males and more often covered with mud), behaviour (they were inactive and rarely courted females) and performance (they were slow crawlers, ineffective courters and easily outcompeted by other males in mating trials). 'She-maleness' was not a characteristic of a particular subset of males, as envisaged in previous work; instead, it was a transitory phase that most (perhaps all) male snakes passed through soon after they first emerged from the winter den. Recently emerged males spent their first day or two relatively inactive, while restoring physiological functions (including locomotor performance and courtship ability). Experimental application of female skin lipids on to males dramatically decreased courtship levels of the recipient snakes. Thus, recently emerged males may derive two kinds of benefit from mimicking female skin lipids. First, female mimicry 'switches off' the male's own (energetically expensive) courtship at a time when that courtship would be unproductive. Second, it may disadvantage his rivals by distracting them from females, and increasing their energy expenditure. Copyright 2000 The Association for the Study of Animal Behaviour.     

Mating behavior ofPhytoecia rufiventris Gautier (Coleoptera: Cerambycidae)

Sexual behavior between males and females, as well as between males, is described and discussed for the cerambycid beetlePhytoecia rufiventris. The beetles' taxis toward plants taller than average height brings the sexes together from a distance. A male may mount another individual (male or female) and attempt copulation without sex discrimination. The male can discern the sex of another individual only when the terminal part of his abdomen touches the ventral surface of the fifth visible sternite of the latter. No evidence of a sex pheromone is found in this species. Within 1.5–5.5 cm the substrateborne vibrations produced by a moving individual may be the important factor which elicits males to approach a moving individual and attempt copulation. If a female is receptive when a male touches her, he can copulate with her without any courtship display. However, if the female runs away and appears unreceptive, the male will perform courtship displays. Copulation is usually terminated by males. Homosexual behavior between males is discussed.     

How Pronghorn Females Avoid Inbreeding Depression

After a bottleneck in a closed population of pronghorn (Antilocapra americana), some inbred matings occurred, and we detected significant inbreeding depression. But inbred matings occurred less frequently than would be expected by chance. Pronghorn females chose mates after a sampling period and had complete control of the mating decision. Therefore, to discover the behavioral mechanism by which females avoided mating with close kin, we studied female movements and courtship sequences. When females moved from one harem to another in the sampling process, they did not shift to harem males of lower coancestry as they approached estrus. Rather, females progressed more slowly through the later courtship stages when the harem male was related vs. unrelated. Also, the rates of male courtship acts were higher within unrelated vs. related pairs. Some females appeared to use multiple mating as an inbreeding avoidance strategy. Our results suggested that inbreeding avoidance by female pronghorn occurred primarily by reactions to the late stages of male courtship, rather than by spatial avoidance of related males.