Choice and utilization of oviposition sites by female Calopteryx maculata (Odonata: Calopterygidae)

Summary Females of the damselfly Calopteryx maculata (de Beauvois) initially choose the larger of a pair of adjacent oviposition sites, about 70% of the time (Table 1), or whichever of two equal sized sites had other ovipositing females on it (about 88% of the time-Table 2). These criteria for initial choice between a pair of sites also interact. Incoming females generally (57 to 74% of the time-Table 3) joined others on the small site rather than ovipositing alone at the adjacent, bigger site. When pairs of large and small sites were replicated across eight locations, there were nonsignificant trends towards greater utilization (eggs laid) of the larger of a pair of oviposition sites within locations (Table 4). The lack of agreement between initial choice and utilization shows that other factors besides size are important in the choice and use of oviposition sites. These include disturbance by males, the presence of other females and choice criteria that can only be assessed during oviposition. When all sites at the eight locations were equal in size, there was considerable day to day and location to location variation in eggs laid (Fig. 1). Viewed over periods of several days, some sites are obviously less attractive than others in terms of cumulative numbers of eggs laid at them. When the amount of vegetation was varied among locations, those with the bigger oviposition sites were used more often, somtimes significantly so, but there were also significant reversals (small sites used more often) (Table 5, Fig. 1). Thus, there is no simple effect of size on the utilization of oviposition sites by Calopteryx maculata females, despite a clear tendency for females to make initial choices based on this criterion. The considerable among and within location variation in number of eggs laid may reflect additional choice criteria or the interaction of size, the presence of other females, disturbance, and location.     

Females prefer larger leks: field experiments with ruffs (Philomachus pugnax)

Summary Preference by females for choosing mates at male aggregations has been hypothesized as the primary selective pressure favoring the formation of leks, but alternative hypotheses account for lek formation without invoking female preference. Observational studies to determine whether male mating success increases with lek size, as predicted under the female preference hypothesis, have produced inconsistent results, possibly due to covariation of lek size with other variables or to male-male or intersexual conflict over lek size. We tested whether females prefer larger leks in a field experiment with ruffs (Philomachus pugnax), a lekking sandpiper, in which male group size, composition, and location were controlled. Wild females chose the larger of two adjacent groups often enough such that males in larger groups had significantly higher per capita rates of female visitation (Table 3). Such behavior would probably lead to higher per male mating rates at larger leks, which is generally considered a necessary condition for female choice to select for lek display (Fig. 2). Lek size in nature will reflect both female preference for larger leks and competition among males, which may favor smaller lek size. All else being equal, however, female ruffs preferred to visit larger groups strongly enough to maintain lekking by males.     

Conditional lekking in ruff (Philomachus pugnax)

Summary In our study of ruff, a lekking shorebird, we found that the lek ratio — the proportion of the total population of males occurring on leks was low, averaging 12% over the breeding season (Fig. 1D). Off-lek males spent approximately the same proportion of time as lek males in displaying to females (Fig. 4). We defined three spacing tacties that male ruffs use to position themselves to court females: Following — directly pursuing females, and two types of lekking behavior, Intercepting — waiting for females at resource-rich sites, and True Lekking — waiting for females at places without any resources other than the males themselves. Males switched among these tactics, causing the lek ratio to vary over the season (Fig. 1 D). Lek ratio increased when the number of females present in the study area plummeted at the end of May, and was positively correlated throughout the season with the copulation rate of the preceding day, suggesting that males were tracking the behavior, as well as the number, of females available (Table 1, Fig. 1). Early in the season, males off leks spent most of their time feeding (Fig. 4), and lek ratio was positively correlated with temperature (Table 1), suggesting that some males may have been unable to lek during cold weather. Males on leks mated at significantly higher rates than Followers (Table 4). On average, males at our interception lek were less site faithful and less peristent than males at true leks, and the interception lek itself disappeared after females stopped coming to use its adjacent resource (Table 2, Fig. 5). The most successful individuals in our population were the True Lekking males, rather than the Interceptors.In addition to the conditinal lekking tactics described here, ruff display a dimorphism in behaviorat leks. Independent males defend small courts on leks, while Satellite males share courts and mutually display with independents Both independents and satellites may use all three conditional tactics. We propose that satellites evolved as specialized. Followers, adept at tracking the movements of females among leks.     

Habituation in the green frog, Rana clamitans

Habituation and its role in the dear enemy effect was investigated in a population of green frogs, Rana clamitans. Green frogs have a prolonged breeding season, and males defend territories centered around suitable oviposition sites. We tested the prediction that male green frogs will habituate to broadcasts of synthetic conspecific stimuli. Our results indicate that male green frogs can discriminate familiar from unfamiliar stimuli. We suggest that habituation helps to mediate the territorial interactions between male green frogs. Strangers present a greater threat than familiar neighbors. By habituating to the advertisement vocalizations of their near neighbors, males avoid costly interactions with individuals that are not a major threat to their territories. Received: 20 July 1998 / Accepted after revision: 6 September 1998     

Aggregation during oviposition and predation risk in Sympetrum vulgatum L. (Odonata: Libellulidae)

Summary Tandem pairs of the libellulid dragonfly Sympetrum vulgatum always start oviposition with contact guarding directly over the surface of shallow water, where they are exposed to green frogs (Rana esculenta). Tandems which approached locations with other pairs already present started oviposition nearby regardless of whether or not predators were actually present. With predators present attack rates during arrival were lower on tandem pairs in groups than on pairs that oviposited alone. During oviposition the attack rate on groups was similar to that on solitary pairs, but predation risk to individual tandem pairs was lower due to dilution effects. Predation risk during tandem oviposition was similar for both sexes, but females had a higher risk of falling prey to frogs during post-tandem oviposition than males. If tandems were attacked by frogs, females left the site after tandem oviposition despite the male hovering above her, and the frequency of non-contact guarded post-tandem ovipositions was reduced.     

Prolonged copulation: A male ‘postcopulatory’ strategy in a promiscuous species,Lygaeus equestris (Heteroptera: Lygaeidae)

Summary Copulation in Lygaeus equestris L. (Heteroptera, Lygaeidae) is known to last 0.5–24 h. Variations in copula duration of field-collected insects were studied in the laboratory, and different hypotheses concerning the significance of prolonged copulations were tested.Through reciprocal matings with normal and sterile (irradiated) males, sperm displacement was estimated at about 90%. A male could thus increase his fitness by preventing subsequent matings of an inseminated female.Copulations with virgin insects, observed over 15 h, were classified in two categories: short (0.5–8.0 h) and long (> 15 h) duration (Fig. 1). No difference in the number of fertilized eggs was found between long and short copulations, and the insemination rate was highest during the first hour of a couplation (Fig. 2). Long-lasting couplations did not give rise to increased sperm displacement (Table 2). These results indicate that there is no difference in the amount of sperm transferred during short and long copulations and that no insemination takes place during the latter part of a prolonged copulation.Longer lasting copulations occurred when the sex ratio was male-biased than when it was female-biased (Fig. 1). The frequency of prolonged copulations was higher when the female was gravid than when she contained no eggs (virgin) (Figs. 3 and 4). Support is thus given to the hypothesis that prolonged copulation is a male postinsemination strategy to prevent subsequent matings of a female.Females subjected to male competition over a longer period, laid fewer eggs and died earlier than females that were mated but subsequently isolated from males (Fig. 5). Egg batches from females living with males were larger than batches from mated, isolated females (Table 3). This is probably due to a combination of many matings with short intermissions and prolonged copulations, both of which postpone oviposition.Comparisons between copulations of males with either gravid or virgin females during these experiments, led to the conclusion that short copulations with virgin females result from a male decision to terminate copulation after insemination is completed, whereas copula duration with gravid females is more likely to depend on a combination of male and female behavior.     

Duration of paternal care in pine engraver beetles: why do larger males care less?

Male pine engravers, Ips pini (Coleoptera: Scolytidae), assist their mates during reproduction by removing the debris that accumulates while females excavate oviposition tunnels in the phloem tissue of host tree bark. Although duration of paternal care and male reproductive success are positively correlated, large males leave their mates and brood sooner than small males. We address two hypotheses to explain the earlier departure of larger males from their breeding galleries: (1) females oviposit most rapidly when paired with large males, thereby reducing the length of time that paternal care increases male reproductive success, (2) larger males have better prospects for future reproduction, and thus leave their galleries in search of new breeding opportunities sooner than smaller males. Contrary to the first hypothesis, when females were paired either with large or small males, there was no effect of male size on their rate of oviposition. Consistent with the second hypothesis, males that initiated breeding galleries were larger than males from the general population. In addition, large males flew farther and faster on flight mills than small males, which may indicate that large males have an advantage in locating suitable breeding sites. Thus, we suggest that large male pine engravers leave their galleries earlier than small males because large individuals have better prospects for future reproduction. Received: 30 November 1997 / Accepted after revision: 23 May 1998     

The costs of male parental care and its evolution in a neotropical frog

Summary Parental care is practiced exclusively by males of the Puerto Rican frog, Eleutherodactylus coqui. Males brood clutches of direct-developing eggs in non-aquatic nest sites and defend eggs against cannibalistic nest intruders. Here, I report on energetic and mating costs incurred by males that provide parental care, and suggest how these proximate costs affect male fitness and the evolution of male parental care in this species. Energetic costs are small for brooding males in comparison to non-brooding, calling males. Brooding males had a higher frequency of empty stomachs and lost small, but significant, fractions of their initial body mass during parental care. Abdominal fat bodies of brooding males during the middle third of parental care were significantly smaller than those of calling males; those of males brooding eggs in earlier or later stages were not different. The mating cost of parental care is greater. Most brooding males cease calling during parental care. However, gravid females are available (i.e., known to mate) on most nights during the principal breeding season; hence non-calling males miss potential opportunities to mate. A mating cost was estimated by calculating nightly mating probabilities for calling males in a plot where nightly calling male densities and daily oviposition schedules were known. On average, a male exhibiting normal calling behavior would be expected to obtain a new mate once every 35.7 days. Hence a brooding male that ceased calling for a 20-day parental care period would miss, on average, 0.56 additional mates. Males that were more successful than average in attracting mates could miss up to 1.63 matings. A marginal value model (Fig. 1) is used to analyze the net effect on male fitness of parental care benefits and costs in E. coqui (Fig. 3). The model indicates that males garner the highest reproductive success by providing care from oviposition through hatching. There is no stage during the pre-hatching period at which a desertion strategy would yield higher reproductive success. In fact, the model suggests that males should provide full parental care even in the face of much higher mating costs than currently obtain in the system.     

Competition with flies promotes communal breeding in the burying beetle,Nicrophorus tomentosus

Communal breeding through nest-sharing may benefit cooperating individuals indirectly, in increased inclusive fitness, or directly, when environmental constraints reduce the fitness of solitary breeders. Burying beetles provide extensive parental care and can breed either in pairs or in larger groups of unrelated males and females. Parentage of communally-reared broods is usually shared but is skewed in favor of the individuals of each sex that provide longer care. Females provide care longer than males, and two females are more likely to remain together in the brood chamber than two males are. Flies and other burying beetles are the major competitors for carcasses and this study suggests that it is competition with flies that promotes communal breeding inNicrophorus tomentosus On medium-size carcasses (35–40 g) the presence or absence of oviposition by flies had a significant effect on the size of the brood reared, and on large carcasses (55–60 g) the number of beetles present, two or four, had a significant effect on brood size. On both medium and large carcasses, pairs rearing broods on flyblown carcasses had fewer young than pairs on clean carcasses or foursomes on flyblown carcasses. There was a strong trend for an interaction effect between number of beetles and competition with flies (Table 1). Duration of parental care was not affected by competition with flies except for that of the first male to depart, which provided care longer on flyblown carcasses (Table 2). Pairs and foursomes were equally able to defend the carcass and brood from conspecific intruders and from larger intrudingNicrophorus orbicollis (Table 3).     

Advantages and a disadvantage of large size for male gammarus pulex (Crustacea: Amphipoda)

Summary The breeding system of the freshwater amphipod Gammarus pulex includes a precopulatory guarding phase by a male. The length of this guarding phase is investigated with respect to a male's size and the number and size of his competitors. As the absolute number of competitors increases, so does the guarding time but as the absolute number of available females increases, the guarding time decreases. Takeovers of the females by unpaired males are more frequent in longer precopulas (Table 2). In contests for females, larger males have two advantages over smaller males; they are better able to make a takeover (Table 2) and better able to resist takeover attempts while paired (Table 3). Males increase the length of the guarding phase as the mean size of their competitors increases (Table 4). When not paired males are usually searching for available females, perhaps in the stream current. Females are unaffected by current speed but increasing current causes decreased male survivorship (Table 5) and increased precopula duration (Table 5). Searching in currents is more dangerous for larger males than smaller ones. It is proposed that the male size distribution observed is the result of selection pressure to increase size from male-male competition balanced by selection against large size while searching for females in the current.     

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.     

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.     

Alternative mating strategies in the water strider Gerris elongatus (Heteroptera,Gerridae)

Summary Males of the water strider Gerris elongatus established territories which included copulation and oviposition sites (small pieces of fallen bamboo). Males were aggressive and competition for territory and females was observed frequently. Male midlegs were more developed than female midlegs and were used as weapons. Reproductive behaviour changed as the breeding season advanced. Early in the season immature females were attracted by male surface wave courtship signals, then copulated white floating on the water surface without ovipositing (type 1). In midseason, males established territories, produced calling signals and attracted females which copulated and oviposited there with male postcopulatory guarding (type 2). In late season, many females oviposited without postcopulatory guarding on pondweed mats near fallen bamboo. Non-territorial males waiter for the arrival of these females and copulated without courtship, but mating success was low (type 3). These alternative mating strategies appeared to depend on differences in male size. Larger males were superior to smaller males in many ways (establishing territory, fighting, mating etc.). The largest males defended territories and had higher mating success than small non-territorial males. Medium sized males used all three strategies according to the number of empty territories and seasonal femald distribution.     

The evolution of leks through female choice: differential clustering and space utilization in six sympatric manakins

Summary The degree to which lekking and non-lekking male manakins select display sites in order to maximise proximity to females was examined by contrasting movements of females with male dispersion. Data on female visiting patterns, male courtship disruption, and mating skew were also collected over three successive breeding seasons. For the five lek-breeding species, female home-ranges were 3–7 times larger than those of adult males. Female movements were concentrated around leks, fruiting places and stream bathing sites. None of the females monitored by radio-tracking expanded her normal range in order to visit males on leks. On the contrary, feeding bouts of females frequently preceded a visit to potential mates at neighboring leks. Despite small sample sizes, significant correlations were found between female home-range size and male clustering (distances between neighboring leks and distances between neighboring males), as predicted by the female choice model and the hotspot model. Adult and immature male home-range sizes were not significantly correlated with male dispersion or female ranges. On the other hand, males and females of the only non-lekking species exhibited similar use of space and home-range size. Male settlement at sites with high levels of female traffic showed that the hotspot model is adequate to explain differences in male dispersion among sympatric lekking species. Comparisons with other studies suggest that apparent female choice could be overidden by past and present male-male interactions or female mate-comparison tactics. In fact, both the hotspot model and the attractiveness hypothesis appear to shape male dispersion on leks: males appear to settle under hotspot conditions with despotic rules generated through bias in female choice or male-male interference. It is proposed that the evolution of leks is ecologically motivated by the spatio-temporal distribution of trophic resources, initially leading to a dispersed male-advertisement polygyny. Following this, a foraging ecology that promotes high mobility by females and the magnetic effect of mating skew in particular males may have favored clustering on exploded leks. Later, the development of male-male interference and the increasing female home-range size could have led to the evolution of classical leks.     

Sex differences in fitness following a group take-over among Toque macaques: testing models of social evolution

Summary A group of toque macaques took-over the home range of one of its subordinate neighboring groups and fused with it to form a larger cohesive group. In the 7 years before the take-over, the dominant group had consistently won all contests at common feeding sites, yet the fitnesses of the females of these two groups did not differ significantly (Fig. 2A). After the take-over the females of the subjugated group occupied the lowest ranks in the combined dominance hierarchy of the merged groups (Fig. 1) and thereby lost the advantages of an own home range, such as priority of access to food. Consequently, in the merged group, survivorship and reproductive success among the subjugated females were significantly less than among the females of the dominant subgroup (Table 2, 4). The dominant matrilines grew numerically and replaced all of the subjugated females, and all but one of their offspring, within 8 years after the take-over (Fig. 2B). These data support the hypothesis that cooperation among female kin in defending resources against strange females is important in the evolution of female-bonded groups. Before the merger all 5 natal males of the subordinate group had transferred to the dominant group, where they occupied high and mid-level dominance ranks (Fig. 1). These males survived at a significantly greater rate than their subordinate female kin. Thus, the cost of group transfer seems to be greater for females than for males, and this may be one reason that females generally do not emigrate or that groups do not fuse. The data suggested three hypotheses. First, since large body size and other adaptations for fighting, giving males an advantage in male-male competition for mates, are also of advantage in resource competition with males and females, such male characters may also be favored by non-sexual selection, especially where male reproductive strategy involves group transfer. Second, female bonded groups evolved as female defensive coalitions against not only female but also male resource competitors, there having been a mutual influence in the coevolution of large-sized males and female gregariousness. Third, female defensive coalitions against large-sized aggressive males are also advantageous out-side the context of food competition, or, independent of foraging strategy.     

Male morphology and behavior correlate with reproductive success in the American redstart (Setophaga ruticilla)

Summary In a population of American redstarts (Setophaga ruticilla), we determined whether a relationship exists between seasonal reproductive success (RS) and a variety of male and female morphological and behavioral characters including plumage and male song. Adult males differ dramatically in plumage from yearling males and also exhibit variable amounts of black on their breast (bib size). Adult males were more successful than yearlings in terms of the number of eggs laid by their females. Among adult males, those with smaller bibs (less black) had females that laid more eggs, and produced more hatchlings and more fledglings. We found no evidence to indicate that this result was a consequence of territory quality. We examined a number of features of song but none alone was a predictor of RS; however, one song feature (rare repeat song) correlated with bib size. When bib size and rare repeat song were analyzed simultaneously, both were found to relate to RS. No female features were predictors of RS, but females arriving earlier at the breeding site mated with males with smaller bibs. The evidence is consistent with the view that plumage of redstarts may be used as a basis for female choice. Offprint requests to: R.E. Lemon     

Reproductive trade-offs from mating with a successful male: the case of the tephritid fly Anastrepha obliqua

In lekking species, females may become sperm-limited when mating with sexually successful males, and this may be exacerbated by a poor male diet. Polygynous males may also be limited by the amount of accessory gland products (AGPs) they can transmit to females, which in turn may influence the females’ refractory period and longevity. Here, we tested the effect of male mating history, larval and adult diet on copula duration, mating intervals, female fecundity, fertilisation success, life span and likelihood to remate using sexually successful males of the lekking tephritid fly Anastrepha obliqua. Flies originated from either a native or exotic host fruit and were protein-fed or deprived. Male diet and larval host influenced copula duration, while the time elapsed between matings was affected by the interaction of mating order and male adult diet. Female fecundity was not influenced by female position in mating order or protein inclusion into the male diet. However, mating order and male larval diet influenced female fertilisation success. Importantly, as males mated successively they were less able to induce a refractory period on females, as the last females to mate with a male were more likely to remate and had slightly longer life spans than the first females to mate with males. These results might be attributed to a decrease in male AGPs with increasing male mating frequency. We discuss the role of conditional expression of male mating frequency with respect to A. obliqua’s life history, the trade-off that females face when mating with a successful male, the effect of larval diet on adult sexual performance and the possibility for sexual conflict to occur due to high male mating rates and fitness costs to females.     

Why insects swarm: testing the models for lek mating systems on swarming Empis borealis females

Summary Female dance-flies, Empis borealis L., gather to swarm, and males carrying nuptial gifts visit swarms for mating. Field observations and experiments were performed on this behaviorally sex-role reversed species to test models of lekking behavior. The key predictions were: (1) female preference model: male visiting rate and mating rate should increase with the number of females in swarm (swarm size), (2) hotspot model: male visiting rate should be independent of swarm size, and (3) hotshot model: swarm size should be positively correlated with the body size of the largest female in swarm. We found that male visiting rate and mating rate increased with swarm size, and that mating rate per female increased with swarm size. Males also mated more often in larger swarms than in smaller ones. Both males and females visited swarm sites even in the absence of other individuals. When females were successively removed from swarm sites more males than females on average arrived at these sites: 2.25 males per female. When no individuals were present at the swarm site, arriving males moved on to another site, whereas arriving females generally stayed. Larger experimental swarm-markers attracted both more males and more females and even more males when swarming females were present. There was no correlation between mean or median female size in swarms and the number of females in swarms. Thus, the female preference model and the hotspot model were corroborated, while other models were judged unlikely to explain swarming behavior in E. borealis. Correspondence to: B.G. Svensson     

Significance of spectral and temporal call parameters in the auditory communication of male grass frogs

Summary During the spawning period, male grass frogs (Rana temporaria L.) frequently produce short and long territorial calls in addition to mating calls. The calls differ in mean pulse number, duration, and pattern of amplitude modulation. Experiments in which recorded natural calls are played back reveal that male grass frogs are capable of discriminating the different conspecific calls. A male frog stimulated by mating calls always responds by producing mating calls in greater numbers (Fig. 3). Territorial calls presented at low intensity also cause an increase in the mating-call rate (Fig. 4), but at high intensity they clicit territorial calls and turning toward the loudspeaker. A combination of short and long territorial calls was especially effective in eliciting the phonotaxis response. As play-back experiments with simulated calls show, the carrier frequency and the pulse repetition rate are particularly important cues for recognition of conspecific calls (Fig. 5). A simulated call with a 400-Hz carrier frequency (the dominant frquency of the mating call) is just as effective as the natural call with the complete frequency spectrum (Fig. 3), whereas a 1100-Hz simulated call is ineffective (Fig. 5). The chief factors in discrimination among the conspecific calls are the call repetition rate and probably the amplitude and frequency modulation. Changes in the duration of the calls had little effect (Fig. 6). The available evidence suggests that the mating call has a reciprocally stimulating action on males in a chorus, whereas the territorial calls experess aggressiveness and give warning to other males.     

Sexual chases in sand martins (Riparia riparia): cues for males to increase their reproductive success

Summary During the pre-laying and laying stages of the breeding cycle, female sand martins are guarded by their mates and chased by other males seeking promiscuous copulations. Because females become exceptionally heavy when they are most likely to be fertile, their increased mass was thought to present cues during flight to males seeking promiscuous copulations. Heavy female sand martins released from the hand were selectively chased in sexual chases (Figs. 1, 2). Breeding females were heaviest during laying and pre-laying (Fig. 3), exceeding any masses normally achieved by breeding males (Fig. 3). A sample of naturally heavy females and birds whose mass had been experimentally increased to that of laying and prelaying females took longer to reach ascending flight, as determined by analysis of video recordings, than a sample of lighter birds (Table 1). It was concluded that this and other flight cues may be detected by males so that they may achieve extra-pair copulations and hence increase their reproductive success.