The Hilltopping Mating System of Leschenaultia adusta (Loew) (Diptera: Tachinidae)

Males of the tachinid fly Leschenaultia adusta perch on small trees and shrubs on the highest parts of Usery Peak in central Arizona. Individuals select twig perches on the downwind side of these plants and fly out spontaneously from time to time or in response to another passing insect. Conspecific males elicit chases that on occasion escalate into elaborate, high-speed pursuit flights that go back and forth near the plant for several minutes. Although several males sometimes perch together briefly in the same plant, typically only one individual remains at a site for more than an hour on any given day. These site-faithful males can be considered territorial residents; they constituted about one-quarter of the males marked during the study. More than half of these residents returned to the same perch plant for two or more days. Perch plants varied in their attractiveness to male flies; male preferences were largely consistent across two years of study. Given that females were occasionally observed mating at male-occupied plants, we place the mating system of L. adusta within the hilltopping territorial category in which males compete for landmark perching sites attractive to receptive females. As is true for other hilltopping insects, receptive females of L. adusta appear to be rare and widely distributed.     

Influences on variation in territorial tenures of male white-faced dragonflies (Leucorrhinia intacta) (Odonata: Libellulidae)

Some individuals in species with extended periods of territorial occupancy may change territory locations within a single bout of territorial activity. Length of occupancy of mating territories among males in a local population of white-faced dragonflies (Leucorrhinia intacta) varied from more than 6 h to 15 min or less. Males with short tenures often established territories in several locations on the pond during a day. Several hypotheses have been proposed to explain shifting territorial sites rather than remaining in a single site during one bout of territoriality. We attempted to test the hypothesis that males shift to leave low-quality sites. Site quality may be affected by costs of defense in relation to intruder rate and the mating benefits of holding the territory. To test whether variation in these possible effects of benefits and costs of territoriality influenced tenure, we manipulated local quality of oviposition substrate and perch density. The quality of oviposition substrate, but not perch density, influenced both potential benefits and costs of territoriality. Female density was higher in areas with good substrate, but so were rates of males intruding into the territories, rates of chasing by territorial males, and local density of territorial males. More matings occurred in areas with good substrate, but among males with tenures of 15 min or more, mating success per male and tenure lengths did not differ statistically among treatments. Defense costs were low for all treatments and perhaps were not an important influence on tenure duration. Territorial males in this population probably adjusted local density to expected mating success by initial choice of site rather than by varying tenure length. Variation in tenure length at a site resulted, in part, from stochastic external factors, such as predation attempts.     

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.     

Postural Changes Accompany Perch Location Changes in Male Butterflies (Asterocampa leilia) Engaged in Visual Mate Searching

Males of the nymphalid butterfly Asterocampa leilia perch and wait during the morning at places where females are likely to appear. Males leave their perches to court passing females and chase away intruding males. As air and ground temperatures rise during the morning, males switch from perching on the ground to perching off the ground (average height = 0.87 m) for thermoregulatory reasons. To evaluate how this switch in perch location might affect mate detection, I have investigated how the three-dimensional posture of the male's body and head varies with perch location and how conspecifics fly through male perching areas. The body posture of males varies with perch location, as measured by pitch and roll relative to gravity, and yaw relative to the sun. Moreover, the pitch and roll of the head relative to the body is adjusted in a way that compensates for variation in body pitch and roll. These results, along with information on conspecific flight altitudes, suggest that when a male is perched on the ground his visual system is positioned in such a way that he is less likely to detect conspecifics flying nearby than when he is perched off the ground. Hence, it appears that early in the morning visual detection of mates and intruding males may be compromised by thermoregulatory concerns.     

Male Reproductive Behavior of the Social Wasp Polistes fascatus (Hymenoptera: Vespidae)

Populations of male Polistes fuscatus simultaneously exhibit two different mate-locating tactics. Some males defend territories in female nesting and hibernation sites. These males frequently do not occupy the same territory each day, and they drag their gasters over perches, which may function to apply a secretion to the perch. Another segment of the population patrols large overlapping areas in female foraging sites. In contrast to territorial males, patrolling males do not rub their gasters on perches, and males seen on more than one day are tenacious to one area. Males in both sites are aggressive to other males and attempt to copulate with females. A laboratory study indicates that large males have an advantage in male-male competition. The mean size of patrollers is smaller than that of territorial males, indicating that patrollers are competitively inferior males. Yet there is considerable size overlap of males between the two sites, suggesting that there is also overlap in the range of probability of mating success between the two sites.     

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.     

Post-copulatory mate guarding by males of the demselfly Hetaerina vulnerata Selys (Odonata: Calopterygidae)

Males of the calopterygid damselfly Hetaerina vulnerata remain with their mates after copulating with them. The species exhibits two unusual features of post-copulatory mate guarding. First, a male will often leave his territory to accompany a female in tandem on a search for oviposition sites elsewhere. Second, a male will perch near his ovipositing female even though she completely submerges when egg-laying and cannot be captured and mated by another male while she is underwater. These activities carry two potential costs: (1) a male may miss other receptive females while guarding one mate and (2) he may lose his territory to an interloper while he is absent. These costs were low, however, because territorial males secured only one mating per 3.6 days on average. Moreover, 23 times out of 26, territorial males reclaimed their plots quickly after being away for 30–60 min. The gain from postcopulatory guarding came from being present to recapture a female should she fly up from the water after rejecting an oviposition site. There was a 40% chance that a female would leave one site to search for another during an oviposition bout. If the male were not present, his mate would be captured and mated by another individual (no female ever selected an oviposition site without being carried to it by a male). Her new partner would fertilize the remaining eggs in the female's clutch (if sperm precedence occurs in this species). The total number of eggs fertilized by a male will be affected by how well he prevents any one mate from copulating again before she lays her entire clutch and the total number of receptive females he captures. The variation in the degree of mate guarding by male odonates seems to be the evolutionary outcome of differences in fitness gains derived from these two competing activities in different ecological settings.     

Rubyspot Territorial Damselflies Behave as “Nasty Neighbors”

Two mutually-excluding hypotheses explain the intensity of aggression between neighbors and their non-neighbors in territorial animals. On one hand, the “dear enemy” hypothesis predicts that territorial animals should be more tolerant towards their neighbors than towards non-neighbors. Conversely, the “nasty neighbor” hypothesis predicts increased aggression towards neighbors than non-neighbors. These different situations depend on who is more likely to be a real competitor, either a neighbor or a non-neighbor, and the intensity of resource competition. Male damselfly of Hetaerina vulnerata defend riverine, mating territories that is the main way to have access to females. These territories are not fixed and so males continuously defend them especially against neighbors. Given this, we tested whether the nasty neighbor principle operates in this species. We monitored a population during an entire mating season, and recorded duration of aggressive behaviors. As a key prediction of the nasty neighbor hypothesis, we expected that such behaviors last for longer when encountering a conspecific neighbor than a conspecific non-neighbor. We also predicted that such duration should be date-dependent as territorial competition could increase in the middle of the season when male density is at its highest. Our results corroborated that aggressive behaviors lasted longer against a neighbor male than a non-neighbor male but there was not effect of date. Thus, neighbors may pose a greater risk and may be a strong selective force than non-neighbors in terms of resource competition. Since neighbor males are continuously trying to widen their territory boundaries (a situation that has been also found in other study systems), an owner male may not even need to recognize his neighbors to fight back.     

Host plant-based territoriality in the white peacock butterfly,Anartia jatrophae (Lepidoptera: Nymphalidae)

Mate locating behavior of Anartia jatrophaewas studied near Ochopee, Collier County, Florida. Males were individually marked, and focal animal samples were used to determine activity, residency, and interactions with other butterflies. We recaptured more than half of 53 marked males within the study area on subsequent days. Marked males restricted non-feeding activity to roughly circular areas typically less than 15 m in diameter. Males showed considerable site fidelity and chased both conspecifics and a variety of other insects. Typically, encountered individuals flew away, and the resident peacock male returned to perch near his previous perch. Encounters with conspecific males averaged 38 sec, three times longer than with other insects. Such site fidelity combined with aggressive interactions indicates territorial behavior. When male density more than doubled, site fidelity decreased, resident turnover increased, and areas that had not been defended at lower density were defended. Without exception, defended sites contained the larval host, Bacopa monnieri.In butterfly mating systems, defense of host plants appears to be much less common than defense of natural features such as landmarks.     

Hilltopping Behavior of Polistes commanchus navajoe (Hymenoptera: Vespidae)

Males of the paper wasp Polistes commanchus aggregate in large numbers on hilltops in central and southeastern Arizona where individual males defend perch sites on shrubs, trees or rocks. Residents chase intruders away quickly and exhibit strong site fidelity at their perches. Takeovers are rare as are prolonged battles for possession of a site. Males have only weak preferences for peaktop perch sites as opposed to those lower on hillsides, and a similarly weak preference for perches in shrubs as opposed to those on rocks. Receptive females appear occasionally at the male aggregation sites to mate with perch holders. The relatively weak territoriality exhibited by P. commanchus may stem in part from the high density of males at peaktops and the correspondingly high rate of interactions. The evolution of hilltopping in a species whose reproductive females are clumped spatially at nest sites poses a puzzle for the ecological analysis of mating systems.     

Mating Systems and Male Size in Australian Hylaeine Bees (Hymenoptera: Colletidae)

The mating systems of seven previously unstudied members of the colletid bee genus Hylaeus Fabricius and one of Hyleoides Smith are described. Male mating tactics can be categorized as territorial (perched males defend flowers or other sites that attract receptive females) or non-territorial (patrolling males search for receptive females at flowering plants). The four species in which some territorial males occur are characterized by: 1. grappling fights among males for preferred perches; 2. territorial control by larger males; 3. the possession of prominent spines or other projections on the venter of the abdomen in larger males; and 4. the occurrence of some males that are as large as, or larger than, the largest females of their species (the ‘large-male phenomenon’). In contrast, the four species that lack territorial males are distinctive in that males: 1. do not engage in grappling contests; 2. lack abdominal weaponry; and 3. are smaller than the largest females of their species. In addition, we searched for the large-male phenomenon in museum collections of four species of Hylaeus that exhibit male abdominal spines (presumed to be the weapons used by territorial individuals) and two other species that lack these attributes (presumed non-territorial patrolling species). The results tend to support the sexual-selection-for-fighting-ability hypothesis, which argues that the evolution of unusually large males is a selective consequence of aggressive male—male competition for access to mates. The limitations of the present data set as a comparative test of this hypothesis are discussed.     

The duration of strong mate-guarding by males of the libellulid dragonflyPaltothemis lineatipes: Proximate causation

Males of the territorial libellulid dragonfly Paltothemis lineatipeschange the intensity with which they guard their mates during an oviposition bout. Immediately after copulation is completed, males exhibit strong guarding, remaining very close to their partners as they begin ovipositing. In less than a minute, however, they begin to drift away to resume territorial patrolling or even to perch while their partners continue to oviposit. The duration of strong guarding is not related to how long the male has been on territory. Nor is it an activity of fixed duration set by the release of the female following copulation or by the initiation of oviposition by a panner. Instead, males can extend the period of strong guarding if oviposition is interrupted experimentally early in a bout. Under these conditions, males follow their mates closely until they have found a new location at which they oviposit steadily. Thus, males apparently must see their panner oviposit for some time before reducing the intensity of mate-guarding.     

Alternative mating tactics in male white-faced dragonflies (Leucorrhinia intacta): plasticity of tactical options and consequences for reproductive success

Summary Alternative tactics used by males to obtain mates usually are associated with genetic and/or phenotypic differences between the behavioral morphs. This system of white-faced dragonfly (Leucorrhinia intacta) alternatives is characterized by plasticity of tactical options for individual males. Males may act either as territorials, and defend small perch-centered territories on the study pond, or they act as transients, spending most of their time in vegetation surrounding the pond and sallying out at intervals in search of mates. The two tactics remain in constant proportions over a broad range of densities, so transients do not result only from a filling in of suitable territorial sites. Males adopt tactics independently from day to day, with no significant influences of phenotypic variation, priority of arrival at the breeding site, or prior success in a role. We interpret this system as based on conditional, frequency-dependent choice of alternatives by a population of males not differing significantly in their abilities to employ one tactic or the other, but we cannot exclude entirely the possibility of mixed strategies. Average daily mating success is equal for territorial and transient males, supporting predictions of mixed and conditional ESS hypotheses. Males of each tactic obtain matings daily in proportion to their representation in the population for most data samples. Deviations from the expected mating success provide no information of use in selecting one or the other tactic on subsequent days. We suggest this system of alternatives represents a conditional mating strategy, in which males adopt tactics based on the availability of perches relative to oviposition substrate and on interactions within and between tactics that are influenced by the relative frequencies of territorial and transient males.     

The Effects of Isolation on the Sensitization and Habituation of Aggression in the Threespine Stickleback (Gasterosteus aculeatus)

Our previous research showed that territorial threespine sticklebacks are more aggressive toward a male conspecific placed in their territory if they have been housed adjacent to a gravid female rather than a male or a nongravid female. This study replicated the condition of a territorial male with an adjacently housed male and compared the results with isolated territorial males. This permitted us to contrast explanations for the increased aggression when the neighbor was a gravid female. If the social context determines the level of aggression, then males with no neighbors (isolates) might be less aggressive because there would be no unique reproductive resource to protect nor any neighbor to protect resources from. Alternatively, if aggression is higher in the isolated group it might be because there was no male neighbor to redirect aggression toward. We found that isolated males were more aggressive toward an intruded male stimulus than males with a male neighbor. The study also provided evidence that sensitization produced by the appearance of an intruding male energizes other aggressive behavior, but not those related to feeding, nor does it cause increase in general activation as measured by increased locomotion.     

Perch selection by singing chaffinches: a better view of surroundings and the risk of predation

Predation risk varies among perches, and the vulnerability ofsinging chaffinches (Fringilla coelebs) might differ dependingon where they perch in a tree. To find out how singing of thechaffinch is associated with antipredatory behavior, I studiedperch selection in mature pine forest and in pine saplings,two habitats differing in the amount of cover for protection from predators. My results show that male chaffinches preferto sing below the canopy of mature pines and in the uppermostparts of sapling pines. Although these are the canopy partsmost exposed to sparrowhawk (Accipiter nisus) attacks, stayingin open sites may be a beneficial strategy for singing chaffinchesbecause it makes it possible to improve antipredatory vigilance.This assumption was supported by the hawk experiments. Afterbeing exposed to the sparrowhawk model, all of the singingbirds selected the conspicuous perch below the canopy of maturepines. The males that perched higher in the canopy before theexperiment moved to the lower canopy, whereas those males thatsang below the canopy did not change their singing perch.     

Song Perch Height in Rufous‐and‐White Wrens: Does Behaviour Enhance Effective Communication in a Tropical Forest?

Animal signals are distorted as they transmit through the environment, but many species have evolved strategies to minimize distortion of vocal signals. Song structure can change over evolutionary time, or signallers can modify their behaviour, to reduce attenuation and degradation in a specific habitat. We investigated signalling behaviour in rufous-and-white wrens, Thyothorus rufalbus , a Neotropical songbird in which both sexes sing, with a specific focus on perch height. Based on previous findings, including a detailed sound transmission study, we predicted that rufous-and-white wrens would choose elevated song perches in order to maximize the distance their songs travel, and that males and females would show different perch height choices. We observed 30 birds in 18 territories in a tropical forest in Costa Rica to determine the perch heights of birds when singing, producing non-song vocalizations, collecting nesting material, foraging, and engaging in other behaviours. We found that both activity and sex influenced perch height. Birds sang from a variety of heights, but the highest perches were used as song posts by males. Males minimized singing from within 1 m of the ground, and they generally perched higher than females, which may reflect sex differences in communication strategies. Both sexes foraged on or near the ground. The finding that rufous-and-white wrens vary their perch height with specific activities suggests that they modify their singing behaviour to enhance long-distance communication.     

Male behaviour in two bumblebees, Bombus nevudensis auricomus and B. griseicollis (Hymenoptera: Apidae)

The mating system of the bumblebees Bombus nevadensis and B. griseicollis involves apparent territorial defence of perch sites near or within visually conspicuous trees. Non–contact chases between perch owners and intruders are rare in B. nevadensis and more common in B. griseicollis. The perches of B. nevadensis are in open areas whereas those of B. griseicoilis are within trees or in sites shaded by trees. The same locations may be occupied on 2 different years. Individual males may return to favoured perches over periods ranging from 2 to 24 days. Males of both species scent–mark spots near their perches early in the morning and then scan visually for passing females for as much as 7–8 h daily. The landmark–based mating system of these bumblebees is similar to that of some other insects and closely resembles the pure dominance (lek) mating system of certain vertebrates. Some hypotheses for the evolution of diversity in male mating tactics among bumblebee species are presented.     

Female choice of sites versus mates in a coral reef fish,Thalassoma bifasciatum

To understand the dynamics of sexual selection, one needs to identify the basis of female choice in mating. Daily censuses showed that most spawns of individual female bluehead wrasses, Thalassoma bifasciatum, occurred at one of several available mating sites, either in a group-spawning aggregation of small males or with a large territorial male. Most females were not located near their principal mating site during the non-spawning period of the day. Females were thus exposed to other males and sites and should have had the opportunity for choice. When a resident territorial male disappeared or was removed experimentally from a mating site, females did not alter their fidelity to that site. Furthermore, manipulations showed that when a territorial male changed the location of his mating activity to an adjacent site, females did not follow him but continued to mate at their customary site. Thus mating sites, rather than the males occupying them, appeared to be the objects of female choice. The bright coloration and courtship behaviour of larger males may demonstrate the safety of a particular site rather than indicating some aspect of male quality.     

Mating behavior and thermoregulation of the reindeer warble fly,Hypoderma tarandi L. (Diptera: Oestridae)

Hypoderma (=Oedemagena) tarandi L. (Diptera: Oestridae) is characterized by a mating strategy in which both sexes meet and mate at two types of distinct topographical landmarks. In the expansive, treeless vidda (= tundra-like) biome, mating places are unique, rocky areas located along rivers and streams or in rocky areas of drying river and stream beds. In wooded valleys below the vidda, flies mated at certain topographical areas along dirt road tracks/paths. Thermoregulatory activities of males occupying perches at mating places included selection of substratum at perch site, orientation of body to sun's rays, crouching, stilting, and flights into upper cooler air. On warm sunny days males perched for just 1–2 min before flying up into cooler air to promote cooling. Laboratory and field studies revealed that flies could not metabolically cool down when held at 25–38°C. Time spent at mating places depended on temperature, duration of sunshine, and wind velocity. Males were very aggressive in pursuing allHypoderma-sized objects that passed by them or that landed near them, but they did not defend specific perch sites. Males either pursued and caught females in flight, or they hopped onto females that landed near them. During 5 years, 74 males and 14 females were seen at mating places. Dissection of six females caught at mating places revealed them to be recently eclosed flies full of fat body and with all eggs intact; two not paired with males were non-inseminated. Three experimentally paired females remainedin copulo for 10, 13, and 19.5 min.