Underwater oviposition in a damselfly (Odonata: Coenagrionidae) favors male vigilance,and multiple mating by females

Summary Female Enallagma hageni oviposit underwater where they are inaccessible to males. I demonstrate that males guard submerged females rather than perch sites, and are behaviorally distinct from lone males at the water. In contrast to lone males, which always attempt to copulate with females presented to them, guarding males exhibit a conditional latency to remating which corresponds closely to the time required by females to oviposit a complete clutch of eggs. By ovipositing underwater, females decrease the risk that their eggs become exposed. Risks associated with submerged oviposition favor both mate guarding, and multiple, within-clutch matings by females. Both guarding mates and lone males rescue females that float on the water surface as the result of improper resurfacing. Such behavior reduces the mortality risk to females from 0.06 to 0.02 per oviposition bout. By remating between bouts, females benefit from the additional vigilance of lone males, who rescue floating females 1.4 times as often as original mates. A second consequence of multiple mating is an increase in the selective advantage of vigilance by mates. Because receptive females become scarce by early afternoon, whereas male density remains high, a male has little (3%) chance of encountering a second receptive female that day. However, he incurs a 42% risk of losing fertilizations if he abandons a mate. For male E. hageni mate guarding functions in the context of both natural and sexual selection. It insures that a mate lives to lay a complete egg clutch in addition to protecting a male's sperm investment.     

The mating system of two hybridizing species of water striders (Gerridae)

Summary We studied oviposition, feeding and mating behavior of the water striders Limnoporus dissortis and L. notabilis in sympatric and allopatric populations occurring on semi-permanent ponds in Alberta and British Columbia, Canada. Here we describe the mating system of the species and consider the evolution and maintenance of reproductive strategies employed by both sexes. Females of both species oviposited along edges of floating vegetation, either with a guarding, postcopulatory male in attendance, or alone and independent of copulation. Some females ovipositing alone were discovered by males, and when pressed for copulation, either (1) abandoned oviposition or (2) copulated and then resumed oviposition. Females that oviposited with a guarding male laid more eggs than those that completed oviposition alone. Most breeding females accepted prey offered experimentally, while a large proportion of males rejected prey but responded to model gerrids with aggressive displays and mating behavior. Males displayed three mating tactics: (1) territorial-signaling (TS), (2) patrol-signaling (PS), and (3) silent patrolling (SP). All territorial males produced surface waves from oviposition sites before attempting to mate. Some patrolling males signaled, while approaching potential mates as an aid in sex discrimination, but others did not signal and mounted both males and females. When presented with dead gerrid models, males of L. notabilis discriminated between sexes while those of L. dissortis mounted both male and female conspecifics. Collectively, males employing TS tactics fertilized more eggs than patrolling males and TS males of L. notabilis fertilized relatively more eggs than those of L. dissortis. Individual males switched frequently between territorial and patrolling behavior both under natural conditions and in field exclosures. TS males gave more signals per encounter than PS males suggesting that signaling varies with male dominance. Choice of tactic did not depend upon hunger level and was not associated with significant differences in body length in single-species populations. However, in a mixed population, the smaller males of L. dissortis were rarely territorial and signaled infrequently.     

Reproductive defence priorities of male willow ptarmigan (Lagopus lagopus): enhancing mate survival or extending paternity options?

Summary Cock willow ptarmigan (Lagopus lagopus) closely guard their mates from predators and conspecific males, and vigorously defend their nests and young. In view of potential costs and benefits of behavioural guarding descisions, I designed a test to examine if, when and how males altered defence priorities. Cock willow ptarmigan were very attentive to their mates throughout the breeding season, unaccompanied hens comprising less than 3% of the sightings of mated females. From the second week of incubation until shortly after hatch, males attempted to guard both mates and offspring. Males guarded mates preferentially over nests until the third week of incubation; they then changed their priority to defence of offspring (nest and/or chicks). The overall defence response initially was strong, but decreased after the first week of incubation. Strength of response increased again in late incubation, and declined as chicks began to fly. Consistency of defence decisions was highest during prenesting and egg laying and lowest during late incubation. Since males defended their mates for a longer period than required for protection of paternity, hypotheses predicting enhanced mate survival and extended paternity options through renesting were examined. Removal of males did not result in reduced survival or increased weight loss of widows during incubation. In light of heavy nest depredation and displacement pressures by conspecifics, mate guarding throughout incubation enhanced male fitness by ensuring paternity in renesting attempts.     

Parental care of nestlings by male red-winged blackbirds

Summary Nestling feeding by males is less common among birds with polygynous mating systems than in monogamous species, because of the pronounced trade-off between parental behavior and the attraction of additional mates. In this study, however, we found that male red-winged blackbirds (Agelaius phoeniceus) commonly assisted females in feeding nestlings in several Ontario marshes. Male parental care was additional to that provided by females, and it significantly enhanced the fledging success of nests (Table 2). Male redwings did not help to feed all nests on their territories: primary and secondary nests were much more likely to receive male parental care than tertiary and later nests. Contrary to expectation, male parental care was not restricted to the nests of primary females: a greater proportion of secondary than primary nests were assisted (Tables 4a and b). The presence of new females settling on the territory at the same time that a resident female had nestlings, resulted in males deferring parental care until a later brood. This suggests that males trade off the recruitment of females against parental care to an existing brood. Although the number of nestlings fledging from a male's territory was strongly influenced by the number of females in the harem, males could additionally increase their reproductive success by feeding nestlings in one or more nests on their territories (Fig. 2). The reproductive success of females was significantly enhanced by male assistance in feeding nestlings (Table 3). However, those females not receiving male assistance on territories of feeding males did not suffer a significantly reduced reproductive success in comparison to females on territories of non-feeding males (Table 2). Males varied considerably in the quality of brood care given. We therefore suggest that the quality of male parental care may be a factor considered by females in choosing a breeding situation.     

Role-reversal in katydids: Habitat influences reproductive behaviour (Orthoptera: Tettigoniidae,Metaballus sp.)

Summary Mating behaviour of the katydid Metaballus sp. varies. At sites QS and DB (in 1982) females competed for access to calling males and males chose mates by mating with heavier, more fecund females. At another site (BR) there was no evidence of role-reversal in reproductive behaviour, and males were observed to compete for mates. This species has a large spermatophore, a product of male reproductive glands, that is eaten by the female after mating. Males at the DB site had small reproductive glands. This suggests that some aspect of the QS and DB environments decreases spermatophore production; spermatophores become a limiting resource for females resulting in the reversal in reproductive roles observed at these sites. A field experiment that involved moving individuals from site BR to QS in 1983 determined that mating system was influerced by site (Table 1). At BR, males produced a continuous calling song, a third of the males observed attracted mates, and called for about 30 min before the female arrived; courtship duration was short. Males that were moved from BR to QS encountered a higher density of receptive females as all males attracted females after an average of just 3 min of calling. They changed their behaviour by producing short periodic bursts of song (zipping), and by courting females for long periods of time. The long courtship period may function as as a mate-assessment period for males. The reproductive behaviour of BR males moved to QS differed from that of native QS males only in the length of time spent in copula.     

Mating system of the intertidal copepod Tigriopus californicus

Male Tigriopus californicus clasp immature females (copepodid stages II–V) for a period of up to a week prior to the female's terminal molt; upon maturation (stage VI) the female is inseminated and released. While females can mate anytime after their terminal molt, experiments using electrophoretically-detected genetic markers indicate that each mates only once in her lifetime. No evidence of sperm displacement was observed. Hence, male mating behavior can be interpreted as pre-copulatory mate guarding, a strategy employed to assure that a potential mate has not been previously inseminated. Males minimize the time investment required to insemiate a single female successfully by preferentially choosing to clasp more developmentally-advanced females; males clasped to stage III females will release them in order to clasp stage V females if the latter are present. Since males are capable of multiple mating, under most conditions of population sex ratio, this mating system results in low availability of unclasped, developmentally-advanced females; consequently, males must clasp successively younger (i.e. developmentally less-advanced) females in order to obtain a successful insemination.     

Female nutritional state affects the rate of male incubation feeding in the pied flycatcher Ficedula hypoleuca

Summary Male pied flycatches Ficedula hypoleuca regularly feed their mates during incubation. By experimentally supplying some females with extra food we studied how the female's nutritional state affected her incubation schedule and the rate at which her mate fed her. Females that received extra food spent more time on the nest and shorter periods away from it, compared with control females. This suggests that nest attentiveness is governed by the amount of energy available to the female. When females reccived extra food, males decreased their rate of incubation feeding. They also did so in response to increasing ambient temperatures, whereas incubation schedules were unaffected. We, therefore, conclude that our results support the female nutrition hypothesis, i.e., that the food provided by the male constitutes a significant nutritional contribution to the incubating female.     

Determinants of paternity in the milkweed leaf beetle

Summary Males and females of the milkweed leaf beetle mate for up to 2.5 d in the field; copulation is interspersed with mounted courtship behavior and periods of passive riding on the female's back. In 1985, females mated with up to 10 different males in Bridgeport, New York, and matings averaged 0.75±0.04 (SE) d in duration. Sperm utilization patterns are complex in the milkweed leaf beetle. In the laboratory, mating duration, mating order and the duration of the gap between matings affected paternity. The second male's sperm predominated when a female's two consecutive matings were of equal duration (but were long: 45 h each) or when they were intermediate in duration (15 h each) with a 5 day gap between the two matings. The mechanism of sperm predominance appears to be one of time-dependent sperm removal and replacement. Neither relative nor absolute size of males affected the extent to which they superceded the sperm of rivals. Electrophoretic analysis of paternity at 6 polymorphic loci showed that offspring of at least eight out of 11 mating pairs pairs collected in the field at the end of the 1984 breeding season were sired by more than one male. At least seven of the 11 families produced some offspring that were sired by the female's most recent mate in the field and in no case was the collected male completely excluded from paternity. In a greenhouse plot, males climbed off females' backs a mean of 1.1±0.3 h before oviposition. Females did not oviposit with males on their backs and did not oviposit sooner when males were removed than when males were allowed to remain mounted, indicating that males don't keep females from ovipositing until they can achieve sperm predominance. The close concordance between male disembarkment and oviposition suggests that males remain with females beyond the time when they have superceded the sperm of their prior mates, possibly to guard them from rival males. Although the prolonged mating association of the milkweed leaf beetle cannot be separated into discrete copulatory and guarding phases, the results of this study suggest that prolonged mating enables males both to remove and replace the sperm of the females' prior mates with their own sperm and to prevent females from remating prior to oviposition.     

Re-copulation and post-copulatory mate guarding increase immediate female reproductive output in the dragonfly Nannophya pygmaea Rambur

After copulation, male Nannophya pygmaea dragonflies mate guard by hovering over ovipositing females and repelling conspecific males. Copulation is not always a prerequisite for oviposition in the females of this species because females can store the sperm received during previous visits/copulations. An oviposition episode consists of several bouts of oviposition separated by periods of perching. We conducted two types of male-removal experiments to examine the effects of mating and post-copulatory mate guarding on the oviposition behaviour of females. In the first experiment, we removed all males from the habitat to eliminate the effect of re-copulation, mate-guarding and harassment by males. In the second experiment, we removed males immediately after copulation to eliminate the effects of guarding and other post-copulatory male-female interactions. We compared these experimental data with data obtained under natural conditions. The dipping rate in an oviposition bout was not influenced by copulation or guarding. However, guarded females made more dips per episode than did solitary females. The proportion of time actually spent ovipositing (total bout duration/oviposition episode duration) of guarded females was higher than that of solitary females. Solitary females often oviposited in more than one territorial site, while guarded females usually oviposited within a single territorial site during an oviposition episode. Because males tend to hold territories at sites where egg survival is high, guarded females (and the male guardian) benefit from guarding in terms of egg hatchability. The possible benefits for solitary females are discussed.     

Risks and benefits of lethal male fighting in the colonial,polygynous thrips Hoplothrips karnyi (Insecta: Thysanoptera)

Summary Males of Hoplothrips karnyi (Hood) (Insecta: Thysanoptera), a colonial fungus-feeding thrips, fight each other in defense of communal egg mass sites, where they mate with females that come to oviposit. Fighting males stab each other with their enlarged, armed forelegs and hit each other with their abdomens. Escalated fights occur between large males of similar size. Fights are often lethal; males that died during observations fought more frequently than other males, were stabbed more often and more severely than other males, and were relatively large, but somewhat smaller than their opponents. Large males tend to win fights and guard egg masses, and they secure about 80% of last matings before ovipositions. Guarding males apparently assess female reproductive condition by putting their forelegs partially around females' abdomens; guarding males, but not nonguarding males, mate preferentially with females that have yet to oviposit. Non-guarding males mate with females away from egg masses, sneak matings at egg masses, and occasionally challenge guarding males. Challenges tend to follow matings by non-guarding males at egg masses. Each of four observed or inferred takeovers was followed by the death of the guarding male that lost. Male fighting strategies are discussed in terms of the consistency of lethal fighting with game theory models. Guardin males appear to pursue a classical hawk strategy of escalate until injured or victorious. This strategy may be advantageous because only large males become guarders, the mating success of guarders greatly exceeds that of non-guarders, and high population viscosity ensures that benefits from killing an opponent accrue directly to gaurders. The occurrence of challenges by large non-guarders implies that fighting ability and resource value asymmetries between males change over time; such changes may result from the energetic costs of guarding, injury to guarding males, or depletion of guarding males' supply of sperm.     

Direct and indirect estimates of sperm precedence and displacement in the dragonfly Sympetrum danae (Odonata: Libellulidae)

Summary The non-territorial dragonfly Sympetrum danae shows a high degree of post-copulatory mate-guarding, which suggests precedence of the last male's sperm. Irradiated male techniques revealed that the last male that mates with a female fertilizes an average of 95% (100% in 28% of the cases) of the clutch laid immediately after copulation, irrespective of any previous matings. Sperm volume estimates in both sexes and sperm opacity changes in females at 7 stages of copulation and oviposition indicated that males remove 41–87% of previously deposited sperm from the female's storage organs during the first 5 min of the copulation. Ejaculation takes place during the remaining 10–15 min. We maintain that indirect estimates of precedence in libellulids, based on sperm volume changes, always understimate reality because of the supplementing effect of a first-in, last out mechanism. Because males are skilled at achieving sperm precedence, they are forced to be good guards as well, since a risk of take-overs exists. Females are believed to benefit from contact guarding because it results in a lowered risk of male harassment and predation as well as a lower energy expenditure during oviposition.     

Mate choice in the yellow-shouldered widowbird: correlates of male attractiveness

Recent investigations of male ornaments in sexual selection have used experimental manipulation of tail length in three widowbird species, but only for one of these have correlates of male reproductive success been reported. I examined correlates of male attractiveness to nesting females over two breeding seasons for the polygynous yellow-shouldered widowbird, Euplectes macrourus, in order to discover which cues females may be using to select mates. The black, long-tailed ( 10 cm) males defend large territories and build nest frames, or cock's nests, which females then line and use for nesting. I examined various aspects of male morphology, five behavioral displays, territory characteristics, and the number of cock's nests that males built. Few correlates of mating success were found. The best predictor was the number of cock's nests that a male builds, though one courtship display also correlated with male mating success in 1 year, as did average grass height. Tail length did not correlate with male mating success. A partial correlation analysis confirmed that cock's nests and, in 1 year, grass height, were the primary contributers to male success. Females may choose where to nest primarily on the availability of suitable nesting sites. Long tails may be used by females seeking extra-pair copulations or in male-male competition for territories.     

“Alternative” mating behavior in the swordtails Xiphophorus nigrensis and Xiphophorus pygmaeus (Pisces: Poeciliidae)

Summary The swordtail Xiphophorus nigrensis exhibits three relatively discrete male body-size classes that derive from allelic variation at the Y-linked pituitary (P) locus. Previous studies have shown that larger males have greater relative reproductive success, and that females prefer large males. We describe the mating behavior utilized by males of each size class during individual encounters with females. Small males rely on chase behavior, similar to the alternative mating behavior classified as sneaker in small males of other species. Large males court and intermediate-sized males court or chase, depending on their body size. There is a strong correlation between P alleles for small size (s) and large size (L) with chasing and courting, respectively. The relationship between mating behavior of males of the genotype I is ambiguous. In the closely related species X. pygmaeus, males are of size similar to smaller X. nigrensis males. Paradoxically, these males do not show the courtship display that typifies larger male X. nigrensis and many other species of swordtails, but instead often employ chase behavior identical to the alternative mating behavior in small male X. nigrensis. We suggest that historical and genetic constraints, in addition to current selection forces, might be important factors in explaining the existence of alternative mating behavior in X. pygmaeus.     

Female choice on male quantitative traits in lizards — why is it so rare?

Female choice on the basis of male traits has been described in an array of taxa but has rarely been demonstrated in reptiles. In the sand lizard (Lacerta agilis), and possibly in other non-territorial reptiles, a male's contribution to a female's fitness is restricted to his genes. In order to choose males of high genetic quality, females have to trade the fitness gain against the costs of active choice. In a Swedish population of sand lizards, long-lived males sired offspring with higher embryonic survival compared to offspring sired by short-lived males. In spite of this female sand lizards did not mate selectively with older and/or larger males. There appeared to be mo reliable cues to male longevity; age-specific male body size was highly variable. Furthermore, estimates of male nuptial coloration did not covary with ectoparasite load and, hence, females cannot use male coloration as a cue to heritable resistance to pathogenic parasite effects. When cues to male genetic quality are poor, or inaccurate, and males make no parental investment, we predict that female choice will be rare. Sand lizard females mating with many partners lay clutches with higher hatching success. Thus, females may obtain good genes for their young by multiple mating, thereby avoiding costs associated with mate choice.     

Sperm competition in the damselfly Enallagma hageni Walsh (Odonata: Coenagrionidae): benefits of multiple mating to males and females

Summary Sperm competition was investigated in the non-territorial damselfly, Enallagma hageni. Using irradiated (sterile) male techniques, the last male to mate was found to fertilize up to 95% of the eggs of the first clutch laid after mating. Dissection of females collected before, during, and after copula showed that a male removes a maximum of 87% of the sperm by volume of a previous mate. These data verify an earlier estimate of lifetime reproductive success in this species which was based on mating success, and suggest that indirect dissection methods offer minimum estimates of sperm precedence. Male E. hageni have ample opportunity to benefit from sperm precedence, since at least 10% of the receptive females encountered had already mated once that day, but still contained complete or partial clutches of eggs. Female E. hageni benefit directly from high sperm precedence because it allows them to exchange matings for guarding service by males during oviposition bouts under water.     

The pursuit of extra-pair copulations by monogamous female razorbills: how do females benefit?

Summary Monogamous female razorbills Alca torda actively sought extra-pair copulations (EPCs) in mating arenas outside their nesting colony. Females showed marked variation in promiscuity, defined as the number of EPCs they accepted (0–7), and in receptivity, defined as the percentage of EPC opportunities accepted (0%–100%). The opportunity of females to encounter males for EPCs was measured by (a) the time spent in the mating arena, and (b) the guarding effectiveness of their mates. Females appeared to encounter males and accept EPCs independently of opportunity, which suggests that variation in promiscuity and receptivity is caused by differences in the degree to which individual females might benefit from EPCs. I tested predictions of four hypotheses which propose benefits which females could obtain from EPCs: good genes, genetic diversity of offspring, insurance against infertility of mate, and acquisition of a new mate. No evidence was found to support two predictions made exclusively by the good genes hypothesis: (a) paired males did not achieve greater EPC success than unpaired males, and (b) males who were cuckolded did not obtain fewer EPCs than males whose mates avoided EPCs, suggesting that a male's attractiveness to other females does not ensure his own mate's fidelity. A prediction of both the insurance and good genes hypotheses was supported: females (who in this species retain their mates between years) showed similar receptivity to EPCs between years. This finding contradicts the genetic diversity hypothesis which predicts that in species that lay one egg per year, females who refuse EPCs in one year will accept them in the next. The good genes and genetic diversity hypotheses both predict that females who accept EPCs will behave as if to maximize their chances of being fertilized by extra-pair males. Results contradicted this prediction: females who accepted EPCs were more, rather than less receptive to their mates' copulation attempts than were females who did not accept EPCs. This finding is compatible with the insurance hypothesis which only requires females to store the sperm of extra-pair males, without necessarily being fertilized by it. Insurance against male infertility was the only hypothesis whose predictions were not contradicted by any of the results.     

Male characteristics,parental quality and the study of mate choice in the red-winged blackbird (Agelaius phoeniceus)

Summary A demonstration of adaptive mate choice by females in resource-defence mating systems requires clear predictions as to how females should rank breeding situations (defined by the quality of both the resident male and the territory he defends) so as to maximize their fitness. Since male quality is only weakly correlated with territory quality in red-winged blackbirds (Agelaius phoeniceus), ranking breeding situations in this species will require a consideration of both those parameters independently of each other as long as both vary among males, are predictable before mating, and affect female fitness. Data from a two year study of an eastern Ontario population of this species suggested that two components of male parental quality, nest defence effort and provisioning of nestlings with food, both varied among males and were somewhat predictable. Two measures of nest defence effort were correlated with an index of epaulet size (a reliable predictor of captive dominance rank in this species) (Table 5), and provisioning appeared to be predictable on the basis of both courtship behavior and breeding experience. Our data also suggest that these two components of male parental quality do not covary. Since male provisioning tends to be restricted to the nestlings of the primary and secondary mates in this species, breeding situations must be ranked not only with respect to their manifold quality but also with respect to the mating status of individual females.     

Mate guarding,copulation strategies and paternity in the sex-role reversed,socially polyandrous red-necked phalarope<Emphasis Type="Italic"> Phalaropus lobatus</Emphasis>

In a recent review, Westneat and Stewart (2003) compiled evidence that extra-pair paternity results from a three-player interaction in which sexual conflict is a potent force. Sequentially polyandrous species of birds appear to fit this idea well. Earlier breeding males may attempt to use sperm storage by females to obtain paternity in their mates subsequent clutches. Later-breeding males may consequently attempt to avoid sperm competition by preferring to pair with previously unmated females. Females may bias events one way or the other. We examined the applicability of these hypotheses by studying mating behavior and paternity in red-necked phalaropes (Phalaropus lobatus), a sex-role reversed, socially polyandrous shorebird. Male red-necked phalaropes guarded mates more strongly than other shorebirds. Males increased within-pair copulation attempts during their mates fertile period, and maintained or further increased attempts towards the end of laying, suggesting an attempt to fertilize the females next clutch; these attempts were usually thwarted by the female. Paired males sought extra-pair copulations with females about to re-enter the breeding pool. Multilocus DNA fingerprinting showed that 6% of clutches (4/63) each contained one chick sired by a male other than the incubator, producing a population rate of these events of 1.7% (n=226 chicks). Male mates had full paternity in all first clutches (n=25) and 15 of 16 monogamous replacement clutches. In contrast, 3 of 6 clutches of second males contained extra-pair young likely fathered by the females previous mate. Previously mated female phalaropes may employ counter-strategies that prevent later mating males from discriminating against them. The stability of this polyandrous system, in which males provide all parental care, ultimately may depend on females providing males with eggs containing primarily genes of the incubating male, and not a previous mate.Communicated by M. Webster     

Mating system of the commensal marine isopod Jaera hopeana (Crustacea)

The commensal marine isopod Jaera hopeana Costa, 1853 was reared in the laboratory through 30 generations in the absence of its host, Sphaeroma serratum, to study its development and reproductive behaviour. It was found that adult males take virtually any opportunity to associate with a young conspecific in manca-I stage (first free-living stage) and carry it around in a characteristic position. This male-manca(I) amplexus ends during the manca's first postmarsupial molt (manca-I to manca-II) at an average age of about 9 d after hatching from the marsupium. Entry into amplexus does not alter a manca's molt timing, the duration of the amplexus thus depending exclusively on the manca's age when it joined by a male. Given a choice, males do not prefer manca-I close to molting over those just hatched. With the first postmarsupial molt, long before sexual maturity, female J. hopeana become receptive to mating. Before a female manca is released from amplexus, it is inseminated by its male partner. Sperm transferred to young immature females are stored within special sperm stores until they are needed for fertilization. The male-manca(I) amplexus seems to be a precopula, wherein males wait for their partners to molt and become sexually receptive. Nevertheless, it is inevitable that every second amplexus on average ends unsuccessfully: although manca-I have already been determined irreversibly (and probably genetically) as males and females in equal numbers, adult males are unable to predict which manca-I are potential mates and which are not. Males accept any manca-I as a precopula partner, and even when given a choice they do not prefer female over male manca-I. From the manca-II stage onward, females are continuously receptive to mating for the rest of their life, and mating can occur immediately upon contact of the partners without any significant investment in energy and time (en passant copulation).     

Correlates of male mating success in two species of Anthidium bees (Hymenoptera : Megachilidae)

Summary Field observations were made on the mating behavior of two congeneric species of solitary bees, Anthidium porterae in an arid grassland and A. palliventre in a coastal sand dune habitat. Males of both species exhibited resource defence polygyny and defended hostplants to gain access to females foraging for nectar and pollen. The mating frequencies of marked and measured resident (territorial) males were monitored during periods of continuous observation, following which measurements of territory size and floral resources were obtained. Mating success of A. palliventre males was strongly influenced by territory characteristics: Males that defended small areas with a few rich hostplant patches mated more often than males that held larger territories containing many hostplant patches of low floral density. Large males generally held high-quality sites and thus had a mating advantage over smaller individuals. In A. porterae, on the other hand, male mating success was unrelated to any measure of territory quality. Copulation frequency and male size were positively correlated, however, apparently due to the increased ability of large males to seize and hold females for mating. The two species also differed in the incidence of non-territorial, sneaky males. While absent in A. palliventre, sneaky males accounted for 12% of all mating observed in A. porterae. Males of A. porterae that displayed sneaky tactics mated, on average, as often as resident males. Offprint requests to: E.M. Villalobos