Mating strategies of topi bulls: getting in the centre of attention

In lek-breeding ungulates, only some males defend clustered lek territories, and others defend dispersed territories or are nonterritorial. In this study of lekking topi antelopes, Damaliscus lunatus, we measured male mating benefits directly by observing matings and investigated why the alternative mating strategies coexist. A multivariate analysis showed that proximity to the lek centre had an overriding, positive, effect on male mating rate. With increasing distance to the lek centre, proximity of a territory to a drainage line became increasingly important in enhancing male mating success. On the other hand, costs of lekking were suggested by higher hyaena density on leks, relatively poor body condition of lek males, and more frequent agonistic encounters, with central lek males more likely to sustain bleeding wounds than others. Probably as a consequence of the intense competition for central lek territories, males defending such territories were larger than others and, judging from horn wear, they were also older than resource defenders. Not only did males defending central lek territories achieve the highest instantaneous mating rate and resource defenders the lowest, but the same order was also likely for overall lifetime reproductive success when we took territorial tenure into account. These results suggest that male mating strategies are phenotype limited, as demands on male quality increase with proximity to the lek centre. Copyright 2003 Published by Elsevier Science Ltd on behalf of The Association for the Study of Animal Behaviour.      

Queuing in space and time reduces the lek paradox on an antelope lek

Lek systems, where females often use centrality to assess male quality, highlight a general paradox in evolutionary biology: how can female preferences for males providing good genes persist when consequential strong directional selection is predicted to deplete additive genetic variance in male quality and thereby obliterate benefits of choosiness? An explanation contributing to the resolution of this lek paradox may be that genetic variance is retained when an indirect mate choice cue, such as centrality on a lek, is an imperfect indicator of male genetic quality. Here I investigate whether the presence of alternative male mating tactics limits the reliability of centrality as a quality indicator in lek-breeding topi antelopes. Whereas males establishing territories directly on the central lek were relatively large, smaller peripheral males regularly shifted their territories centripetally and in this way also occasionally obtained central territories. By such opportunistic queuing, small males could increase their mating success drastically; however, their territorial tenure in the lek centre was relatively short, consistent with moderate competitive ability. These results suggest that male topi antelopes can obtain central lek territories through alternative mating tactics, providing scope for variance in male quality on the central lek. In a separate finding, the mating success of central males was found to increase during territorial tenure, independent of estimated age. The demonstration of queuing in both space and time on a mammalian lek highlights the importance of considering male tactical dynamics over time in order to avoid an inflated appearance of the lek paradox.     

Mate choice or harassment avoidance? A question of female control at the lek

Recent studies on the reproductive behavior of fallow deer,Dama dama, propose that harassment from nonterritorial maleshas a major influence on female movements and mate selection,leading ultimately to the evolution of lek mating in this species.In order to support this statement, one must demonstrate thatfemale movements between lek and isolated territories, and amonglek males, lead to a reduction in levels of harassment. We arguethat current evidence in favor of this view is inconclusive.A quantification of the total harassment costs experienced byfemales in lek and isolated territories has never been made.In addition, female movements within the lek may actually leadto higher levels of disruption and harassment: The rate at whichfemales join male territories increases with harem size (thenumber of females present in the territory), even though haremsare disrupted increasingly with size due to a higher frequencyof intrusions by nonterritorial males. Females also join maleterritories at a higher rate while these males are engaged incopulatory sequences, but copulatory sequences are again associatedwith high levels of disruption and harem instability. In theabove studies it is argued that females are nonselective intheir mating preferences. This assessment is based on the findingthat males that adopt different reproductive strategies do notdiffer in their mating rates. Here mating rate is measured asthe number of copulations received per female-hour. There area number of reasons, however, why females exhibiting matingpreferences might remain longer with preferred males, and sothe above preference measure cannot be used to exclude the possibilitythat females are selective. More research is required to identifythe major factors influencing patterns of mate selection andthe evolution of leks in this species. We suggest a number offield tests that may help to identify these factors.     

Red deer females collect on male clumps at mating areas

Mating strategies in mammalian herbivores are adapted to thedispersion of females, and female dispersion is mainly determinedby resource dispersion, although it is frequently unclear whetherfemales may also be influenced by the location of males. Inthe red deer (Cervus elaphus) the distribution of females beforethe rut predicts the places were males should establish territoriesand even their relative success. However, the number of femalesusing the mating areas in Doñana increases during therut. We observed 20 areas of meadows, used by grazing femalesbefore the rut. At the onset of the rut, the number of females increasedin some of these areas and decreased in others, and the opposite patternwas found after the rutting period. Changes in the vegetationat mating and nonmating areas could not account for the changesin female distribution; even some of the highest quality meadowswere vacated by females during rut. In selecting the matingareas, females avoided isolated small meadows within the scrubarea and preferred larger meadows where a number of neighboringrutting males could be found. Females also avoided those areas heavilyused by fallow deer (Dama dama), a competing sympatric species.We found that females suffered less sexual harassment when inlarger harems and when their harem was surrounded by other harems.Our results, together with those in the literature about thispopulation, indicate that red deer females collect during theearly rut in mating areas containing several rutting males,although once there they may select particular sites based on availabilityof food rather than based on the presence of a particular male. Byjoining harems in large meadows they are less harassed, andat the same time they probably increase their chances of matingwith highly competitive males. The results from Doñanasupport the idea that harassment avoidance may lead to femalemovements to areas with male territories without lek breedingor female comparison of male phenotypes and may bring an insightinto those factors leading to clumps of male territories andleks.     

Mate retention, harassment, and the evolution of ungulate leks

Current models of lek breeding mostly suggest that males defendclustered mating territories because females show a preferencefor mating on leks. Here we argue that, in lek-breeding ungulates,males may also gain benefits from holding clustered mating territoriesbecause clusters retain does in estrus. We show that in fallowdeer (Dama dama) harems are commonly disrupted by young males.Bucks that hold territories on the lek that lose their haremsquickly regain does as other harems are disrupted, whereas bucksdefending isolated, single territories rarely regain does thesame day. The risk of harassment may also help to explain whydoes in estrus leave the large, unstable herds that they usuallylive in. Does in estrus are frequently chased by young maleswhen outside male mating territories. Benefits of moving tothe lek (versus moving to single territories) include reducedrisks of long chases. Though intrusions by young bucks are thecommonest cause of does leaving male territories in our studypopulation, other factors that cause does to move between neighboringharems (including disturbance by predators and persistent courtshipby males) may generate benefits to males holding clustered matingterritories. Once clustered mating territories have developed,the additional costs of mate choice are likely to be low, andfemale preferences for particular male characteristics may belikely to develop.     

Black holes, mate retention, and the evolution of ungulate leks

In some ungulates living in unstable herds, females in estrusleave their usual groups and join males defending mating territories.During the 12-24 h before mating, females commonly move severaltimes between males. These movements are commonly caused byharems being disrupted by young males or by overenthusiasticcourtship by the territorial male. When females leave a territorythey typically move to its nearest neighbor. Under these circumstances,clusters of territories can retain estrous females until theymate and leave the lek. This paper develops a model to investigatethe benefits of defending clustered versus dispersed territoriesto males and the consequences of variation in the rate of femalemovement between territories (P_m) and the tendency for femalesto move from one territory to a neighboring territory (a). Wherefemales move between territories at least once every 24 h (P_m< 0.04) and usually move to neighboring territories (a <0.5), the mating success of males is inversely related to thedistance from their territory to its nearest neighbor, and malesdefending clustered territories have higher mating rates thanthose defending dispersed territories. This process may be importantin the initial evolution of ungulate leks, which may resembleblack holes, attracting and retaining estrous females untilthey mate and their estrus ceases. It provides one possibleexplanation of the evolution of ungulate leks that does notrely on female preferences for mating with particular phenotypiccategories of males.     

Correlates of male mating success and female choice in a lek-breeding antelope

We investigated factors underlying variation in male matingsuccess in Uganda kob (Kobus kob thomasi), a lek-breeding antelope.We found that only heavy (and, possibly, relatively old) malesheld lek territories and that female choice was an importantdeterminant of nonrandom mating patterns at leks. Our measureof male mating success was closely related to the historicalpopularity of the territory that a male defended, and individualfemales showed consistent preferences for particular lek territories,despite changes in territory ownership. Male success increasedwith body weight and declined independently of territory effectsduring each bout of lek territory tenure. We also found someevidence that female kob copied one another's choice of matesbecause females arriving at a lek tended to join territoriesthat already had relatively large harems on them. When comparedacross leks, average male mating success increased with leksize. Our results suggest that female kob may use a suite ofmale- and territory-based cues in mate choice at leks and, asa result, mate with particularly large males. However, we wereunable to determine whether female kob gain any direct or indirectbenefits through mate choice at leks.     

Lekking, resource defense, and harassment in two subspecies of lechwe antelope

For lek-breeding in ungulate populations to continue, benefitsto males defending lek territories and to females visiting leksmust outweigh the costs. In this study, Kafue lechwe males onleks gained higher mating rates than nonlekking males, a resultof sexually receptive females leaving herds and aggregatingon leks. When the numbers of females on leks were experimentallyreduced, benefits to males decreased, resulting in males graduallyabandoning lek territories. A comparison with a population ofnonlekking, resource-defending black lechwe showed that matingattempts by estrous females in herds were disrupted by harassingmales eight times more frequently in a population of lek-breedingKafue lechwe than in the nonlekking black lechwe. Despite thefact that there were fewer Kafue lechwe females on single territories,harassment of estrous females by males was greater on singleterritories of Kafue lechwe than on leks and greater than onblack lechwe resource territories. Females were also absenton Kafue lechwe single territories for long periods becauseof erratic, widespread movements of compact herds resultingfrom unpredictable distributions of resources. In contrast,black lechwe females were more evenly dispersed over homogeneousresources and for a given territory, females were likely tobe present most of the time. Therefore, unlike black lechwe,male Kafue lechwe find it uneconomical to defend resource territories.Thus, costs to estrous females mating off leks and the absenceof benefits to males attempting to defend resource-based territoriesmay be important cofactors in the appearance of lek-breedingin some ungulate populations     

An experimental test for body size‐dependent effects of male harassment and an elevated copulation rate on female lifetime fecundity and offspring performance

Many studies investigate the benefits of polyandry, but repeated interactions with males can lower female reproductive success. Interacting with males might even decrease offspring performance if it reduces a female's ability to transfer maternal resources. Male presence can be detrimental for females in two ways: by forcing females to mate at a higher rate and through costs associated with resisting male mating attempts. Teasing apart the relative costs of elevated mating rates from those of greater male harassment is critical to understand the evolution of mating strategies. Furthermore, it is important to test whether a male's phenotype, notably body size, has differential effects on female reproductive success versus the performance of offspring, and whether this is due to male body size affecting the costs of harassment or the actual mating rate. In the eastern mosquitofish Gambusia holbrooki, males vary greatly in body size and continually attempt to inseminate females. We experimentally manipulated male presence (i.e., harassment), male body size and whether males could copulate. Exposure to males had strong detrimental effects on female reproductive output, growth and immune response, independent of male size or whether males could copulate. In contrast, there was a little evidence of a cross‐generational effect of male harassment or mating rate on offspring performance. Our results suggest that females housed with males pay direct costs due to reduced condition and offspring production and that these costs are not a consequence of increased mating rates. Furthermore, exposure to males does not affect offspring reproductive traits.     

Evolution of black grouse leks: female preferences benefit males in larger leks

Leks, communal display grounds in which males display and femalesonly attend to mate, represent one of the most remarkable outcomesof sexual selection. There have been no detailed studies thatcompare the behavior of males and females between leks of differentsizes to test if there is any benefit for male clumping andto test the many hypotheses suggested to explain lekking. Inthe black grouse, Tetrao tetrix, larger leks have many morefemale visits and copulations, leading to a higher average malemating success. Females visiting larger leks are also more likelyto mate, indicating that female preferences of males are importantfor the evolution of leks. Yearling males seldom copulate, buttheir presence on the lek increases the mating success of adultmales, suggesting that lek size per se and not only male qualityaffects female preferences for larger leks. The distributionof males over lek sizes agrees with a game theory model of idealfree distribution with unequal competitors, in which less competitivemales go to smaller leks.     

Resource Defence or Exploded Lek? – A Question of Perspective

It becomes increasingly obvious that animal mating systems cannot be classified into distinct categories, but transitions between mating system classes are continuous. Positioning a certain mating system at this continuum is often not straightforward, however. Depending on which characteristic is considered, a mating system may end up at very different positions on this gradient. Here, we explore the potential conflict between mating system classifications that may arise when they are based on different criteria by investigating the mating system of the cichlid fish Simochromis pleurospilus in which males defend small patches of homogeneously distributed food resources (turf algae) vigorously against food competitors, but they allow specific females to use them. We hypothesized that male defence may generate high‐quality feeding patches serving to attract females, and hence male territoriality constitutes a form of courtship. Our field data show that males selectively allow approximately one‐third of the visiting females to feed on their territory and that females preferentially feed in male territories and usually sample several territories successively. As males protect food patches against other algae grazers and guard females from harassment by food competitors, females gain nutritional benefits from visiting male territories. Hence, males appear to generate essential resources for females, which is the key feature of resource‐defence mating systems, although the distributions of resources and of males and females are characteristics of an exploded lek.     

Male territoriality and mating system in the European beewolf Philanthus triangulum F. (Hymenoptera: Crabronidae): evidence for a “hotspot” lek polygyny

The evolution of the mating system of a species is strongly influenced by the spatial and temporal distribution of females and/or resources. Here, we describe aspects of the territorial behavior of males of a solitary digger wasp, the European beewolf (Philanthus triangulum) and characterize the mating system. We show that beewolf males establish small territories that do not contain any resources essential to females. These territories are intensively scent-marked with a pheromone from a cephalic gland and are defended against intruders in combat flights. We provide evidence that scent-marking constitutes a chemical display and that the pheromone serves to attract receptive females and, thus, represents a sex pheromone. Using spatial statistics, we show that beewolf territories are clumped in space both with respect to other male territories and, more importantly, with respect to female nesting sites. Additionally, the proportion of days a territory is occupied by a male is correlated with the number of female nests in the vicinity. Taking into account that beewolf males do not defend or provide resources essential to females, but merely display chemically to attract females for mating in an aggregation of territories close to female nesting sites, we conclude that the European beewolf exhibits a hotspot lek polygyny with female nesting sites constituting “hotspots” for lek formation.     

When should males lek? Insights from a dynamic state variable model

A central focus in the study of lek evolution is to understandthe clustering of male mating territories. Lekking males typicallydefend small clumped territories and experience intense competitionassociated with dense aggregations. We used dynamic state variablemodeling to evaluate three alternative selective pressures proposedto explain the evolution of lekking. These are female matingbias for large clusters, reduction in predation risk in largeclusters, and male harassment of estrous females. We modeledmale mating decisions during a single breeding season usinga lekking ungulate as a model system. Males could choose fromeight alternative tactics that included a nonreproductive tactic,territorial tactics ranging from low to high clustering, andthe option to join a mixed-sex herd. The model predicted a state-and time-dependent strategy that maximizes mating success overthe course of the season. We then simulated a population of100 males that used the optimal strategy and calculated theproportion of the population that adopted each tactic. Our modelgenerated unique predictions for the three selective pressureswe considered. Female mating bias, when nonlinearly relatedto cluster size, had the greatest potential to generate largeclusters of territorial males, whereas predation risk and harassmentof females typically did not promote male clustering. More generally,our model highlights the conditions that will favor lekking.Lek-like clustering was consistently produced when the benefitsin clustering increased in specific nonlinear ways. Our modelthus emphasizes clarifying the shapes of relationships betweenpotential selective factors and the size of territory clusters.     

Male harassment influences female movements and associations in Grevy's zebra (Equus grevyi)

In traditional models for social organization, female movementsand association patterns track resource distribution, whereasmales track females. More recently, this model has been expandedto include feedback effects of male behavior, especially sexualharassment, on female decisions. In Grevy's zebra (Equus grevyi),males defend territories containing resources attractive tofemales, who form unstable groups. Past research has explainedfemale behavior based on resource distribution and needs alone.Lactating females have been found to have restricted movementsand fewer male associates than nonlactating females, a patternwe find in our study. This pattern has previously been attributedsolely to the higher water needs of lactation. However, in ourpopulation, both lactating and nonlactating females are typicallyclose to water. We test the hypothesis that male harassmentalso influences female ranging and associations with males.This effect is predicted to be greater for lactating femalesbecause harassment has higher costs to them. We find that lactatingfemales experience higher harassment rates than those of nonlactatingfemales. Lactating females tend to move faster during harassmentperiods, whereas nonlactating individuals do not. Lactatingfemales experience lower harassment rates if they spend moretime with a particular male, whereas nonlactating females' harassmentrates do not depend on their allocation of time to a primarymale. We suggest that females concentrate their time with onemale in order to reduce male harassment. Even in species suchas Grevy's zebra without strong male–female bonds, socialinteractions may be a significant driver of female distribution.     

The social organization of feral peafowl

Peafowl are usually reported to have a mating system based on harem defence by adult males. In a small feral population near Oxford, males defended small (<1 ha) territories while females remained in one flock that ignored male territory boundaries. After mating, females become solitary. At no time did a female associate selectively with one male or remain within his territory, nor did males attempt to follow or guard female groups. Two out of four males were seen to mate. These differed from the other two in being neither very old nor very young; they held territories smaller than that of the young male and were no larger or longer-tailed. However, they spent more time displaying. We suggest that peafowl have a mating system similar to a lek: males defending small, clumped territories visited by females for mating.     

Resource defense polygyny by Hetaerina rosea Selys (Odonata: Calopterygidae): influence of age and wing pigmentation

Current evidence suggests that in Hetaerina damselflies males exhibit lek mating system. In this study, in order to answer if the same occurs in Hetaerina rosea Selys, we manipulated vegetation substrates used as territories and quantified the number of visiting females, males defending territories and fight intensity. We also examined whether body size and wing pigmentation are selectable traits in male-male competition, and if age affects male territorial behavior. Our results showed that males with larger pigmented areas won more contests, independently of body size. Old males changed from territoriality to sneaking strategy. Contrary to other Hetaerina species, males of H. rosea do not display lek behavior, but defend resources according to the resource defense polygyny strategy.     

Uganda kob prefer high-visibility leks and territories

In lekking species, where males provide estrous females withlittle more than sperm, it has been widely supposed that theonly possible benefits to females of mate choice are genetic.We studied female choice of leks and territories in a reduncineantelope, the Uganda kob (Kobus kob thomasi), and found thatfemales consistently preferred high-visibility mating sites.Leks were elevated and had shorter grass and fewer thicketsthan the surrounding areas. Changes in the number of male andfemale kob on 10 leks were correlated with changes in surroundinggrass height, and both females and males preferred leks withexperimentally reduced grass height over neighboring controls.Within a lek, territory popularity was the primary determinantof male daily mating success, and females preferred territoriesrelatively far from thickets, but removal of thickets did notaffect female territory preferences. Because lion hunting successon kob increases with grass height and thicket density, femalesmay benefit directly from these preferences by reducing therisk of predation.     

Context-dependent effects of tail-ornament damage on mating success in black grouse

Male black grouse (Tetrao tetrix) may receive damage to theirtail ornaments, the lyre, during goshawk predation attemptsand during fights with other males. In this study we confirma previous observation that black grouse males with damagedtail ornaments suffer reduced mating success. In males thatheld territories on the edge of the leks, tail damage was unrelatedto mating success, whereas in central males damage was negativelycorrelated with mating success. We tested experimentally whetherabsence of damage is used by females in mate choice. In maleswith edge territories, intact, control males had higher matingsuccess than males with cut tails, but in males with centralterritories, lyre cutting had no effect on mating success. Theseresults suggest two interpretations. First, female choice alsodepends on factors other than tail damage such as position onthe lek and dominance. Second, the effect of tail damage iscontext dependent; in males that otherwise meet females standards(e.g., dominant males), the effect of tail damage is negligible,but in less dominant males, tail damage could be used by femalesin mate selection. The second interpretation provides an explanationfor why the data on unmanipulated and manipulated birds differ.In experimental central birds, factors other than tail damageprobably determine male mating success, whereas in experimentaledge birds such factors are probably absent and therefore taildamage is relatively more important. In central unmanipulatedbirds, however, males with natural damage are probably not chosenbecause tail damage and absence of other attractive traits arecorrelated. The absence of an effect on peripheral unmanipulatedbirds may be explained by their overall low mating success     

Interacting effects of predation risk and male and female density on male/female conflicts and mating dynamics of stream water striders

We used a factorial experiment to examine interacting effectsof male density, female density, and sunfish (predation risk)on mating dynamics of the stream water strider (Aquarius remigis).Many of our results corroborated earlier studies on the isolatedeffects of each factor on mating behavior. The effect of eachfactor, however, depended on the other factors. For example,in low density pools, predation risk decreased male generalactivity, male/female harassment rates, mating activity, andmating duration and increased the large male mating advantage.At higher densities, however, water striders apparently enjoyed"safety in numbers" and did not alter their mating dynamicsin response to the presence of predators. Female activity showeda particularly complex response to male density and fish. Whenmales were scarce, fish caused females to reduce their activity.However, when males were abundant, fish increased female activity,probably because fish decreased male activity thus releasingfemales from harassment by males. The three treatment factorsalso had interacting effects on male mating success. In theabsence of fish, when females were scarce, increased male densityresulted in a decrease in mean male mating success; however,when females were abundant, increased male density enhancedmean male mating success. In contrast, in the presence of fish,male density had little effect on male mating success. Manyof the observed mating patterns can be explained by the effectsof ecological and social factors on male/female conflicts; thatis, on male harassment of females and female reluctance to mate.     

Chorus organization and male mating behavior in the Japanese pond frog,Rana porosa brevipoda

Male mating behavior of a Japanese pond frog,Rana porosa brevipoda, was observed in an enclosed pond. Males organized chorus aggregation during the night. Within the chorus, most males defended “floating” territories. Territorial males exhibited 2 types of calls: advertisement and encounter. Mating occurred primarily in male territories with female initiation, while most spawning occurred outside of the territories. After spawning, males returned to their territories and resumed display behavior. The mating system of this frog is analogous to the typical lek system. Alternative male mating tactics, including satellite and ambush behavior, were also observed. Satellite and ambush males mated with females through forced clasping.