Sex-role reversal revisited: choosy females and ornamented, competitive males in a pipefish

In the pipefish Syngnathus typhle sex roles are reversed, thatis, females compete more intensely than males over mates. However,competition over mates among individuals of one sex does notnecessarily prevent members of that same sex from being choosy,and choosiness in the other sex does not prevent competitionwithin it. In an experiment we allowed a female pipefish tochoose freely between two males, after which we released themales and let the three interact. Comparisons with earlier resultsshow that both sexes courted partners and competed with consexuals.However, females courted more often than did males, and courtshipwas more frequent in treatments involving large individualsthan in treatments with small individuals. Males competed amongthemselves for access to mates but for a shorter duration thanfemales in the same situation. Males displayed an ornament towardsfemales but not to males during mating competition. Females,however, used their ornament in both contexts. Females did notalways mate with the male of their previously made choice, whichwe interpret as females being constrained by male-male competition,male motivation to mate, or both. Thus, in this sex-role reversedspecies, mate choice in the more competitive sex may be circumventedand even overruled by mate competition and mating willingnessin the least competitive sex. Hence, sex roles should not beconsidered as sexes being either choosy or competitive but ratherthat males and females may exhibit different combinations ofchoice and competition.     

Behavioral responses of a sex-role reversed pipefish to a gradient of perceived predation risk

Conspicuous behaviors such as courtship and mating often makeanimals susceptible to predation. When perceiving themselvesat an elevated level of risk, animals frequently reduce conspicuousbehaviors in tradeoff for a decrease in probability of beingpreyed upon. In the present study, we used two experiments toexamine the effect of perceived predation risk from cod (Gadusmorhud) on nonreproductive and reproductive behaviors in thesex-role reversed pipefish (Syngnathus typhle). In the firstexperiment, no differences due to predation risk were detectedin the nonreproductive behaviors of either males or females.In the second experiment, predation risk had significant effectson reproductive behaviors. Pipefish were allowed to court andcopulate at four different predation levels. We created predationlevels differing in perceived predation risk by controllingthe number of sensory modes through which pipefish could detectthe presence of a cod. As predation risk increased, pipefishcopulated and courted less frequently, swam alone (displayedand searched for conspecifics) less often, and waited longerbefore commencing courtship. These changes in behavior minimizedthe amount of time spent above the eelgrass and presumably reducedconspicuousness to visual predators. Pipefish also copulatedafter a smaller amount of courtship as predation risk increased,indicating that they may trade information concerning mate qualityfor a reduction in predation risk. No differences were foundin any response variable between males and females. The roleof operational sex ratios and intersexual competition in determiningwhich sex assumes greater costs in mate acquisition is questioned.     

The evolution of courtship rituals in monogamous species

In this paper we propose an alternative explanation for theevolution of courtship rituals in monogamous species. We demonstrate,using computer simulations, how male courtship might developas males exploit response biases in females to manipulate thefemale into starting reproduction before she has been ableto assess the male's intentions. In our coevolutionary simulations, a recurrent, artificial neural network is used to model thefemale recognition mechanism, while the displaying male isrepresented by a sequence of signals. Our particular modelsituation is just one example of how a reproductive conflictcould result in the evolution of ritualized displays in monogamous species. Since reproductive conflicts occur even after pairformations, the explanation we propose may also apply to ritualsthat occur after pair formation.     

Choosy females and indiscriminate males: mate choice in mixed populations of sexual and hybridogenetic water frogs (Rana lessonae, Rana esculenta)

For several decades, behavioral ecologists have studied theeffects of the environment on the behavior of individuals;but only fairly recently they have started to ask the reversequestion: how do the behavioral strategies of individuals affectthe composition and dynamics of populations and communities?Although intuitively obvious, this feedback from individualto higher levels is difficult to demonstrate, except in systemswith exceptionally fast and marked responses of the populationsto the behavior of its members. Such a system exists in sperm-dependentspecies. In European water frogs, for instance, successfulreproduction of a hybrid species (R. esculenta, genotype LR)requires mating with one of its parental species (R. lessonae,genotype LL), except in the rare cases where hybrids are triploid.The sexual host LL, however, should avoid matings with the sexual parasite LR, because the resulting LR offspring willeliminate the L genome from their germ line. In this studywe investigate how this conflict is solved. Since water froghybrids come in both sexes, rather than as females only likein other sperm-dependent systems, we performed the tests withboth females and males. One individual was given a choice betweentwo individuals of the opposite sex, one an LL and the otheran LR. In both species, females showed the predicted preferencefor LL males, whereas males did not discriminate between LLand LR females. On the individual level, we interpret the sexdifference in choosiness by the lower costs from mating withthe wrong species (LR) and the higher benefits from matingwith large individuals in males than in females. In "normal"species, male preference for large (i.e. more fecund) femalesis advantageous, but in this system such a choice can resultin mating with the larger LR females. With respect to the structureand dynamics of mixed populations, we discuss that the observed female preference is consistent with the higher mating successof LL males found in nature. Hence, mate female choice is astrong candidate for a mechanism promoting coexistence of thesperm-dependent hybrid and its sexual host. This confirms predictionsfrom previous theoretical models.     

Preferred males are not always good providers: female choice and male investment in tree crickets

Female tree crickets (Oecanthus nigricornis) prefer large malesbut do not receive larger glandular courtship gifts from thesemales. This finding is puzzling from both the male and femaleperspectives, because females should prefer males providingmore direct benefits, and because males who provide larger giftsachieve higher insemination success. We tested for differencesin the quality of male secretions and found that larger malesprovided more proteinaceous food gifts than did rivals, whichcould explain why they are preferred by females. The preferencein turn could cause depletion of food gift reserves in favoredmales, because natural remating rates are high and because evena single feeding bout negatively affects glandular stores. Mostintriguingly, we showed that preferred males can adaptivelydecrease the size of courtship food-gifts provided (in orderto conserve gifts for future mating events) when they perceivethat the probability of multiple future mating opportunitiesis high. Thus, the elevated mating rates of preferred males(both before and after a focal mating event) could account forthe small size of their courtship food-gifts.     

Increased vigilance of paired males in sexually dimorphic species: distinguishing between alternative explanations in wintering Eurasian wigeon

In animal pairs, males are often more vigilant than females.This is generally assumed to result from mate guarding (eitheragainst predators or other males). However, when males haveconspicuous secondary sexual characteristics, they could beconstrained to be more vigilant because of a higher predationrisk than females. We attempted to distinguish between the "maleconstraint hypothesis" and two variations of the mate-guardinghypothesis by studying the vigilance behavior of the sexuallydimorphic wigeon during early winter, when some males are inbreeding plumage and some are not and when not all males arepaired. The proportion of time spent vigilant by paired malesin breeding plumage was five times higher than any other categoryof males or females. We found no significant differences betweenthe vigilance levels of unpaired male wigeon in cryptic andin breeding plumage and therefore rejected the male constrainthypothesis. As vigilance levels of paired and unpaired femalesdid not differ either, we rejected the hypothesis that pairedmales invest in vigilance to reduce their mate's need to bevigilant to predation risks. Paired females interacted lessfrequently with other wigeon than unpaired ones, and it is probablyto protect their female from other males that paired male wigeonincrease their vigilance times.     

The influence of environmental quality on sexual selection in Nauphoeta cinerea (Dictyoptera: Blaberidae)

We examined the impact of environmental conditions on the sexpheromone and mating behavior of the cockroach, Nauphoeta cinerea.Previous research on this species has shown that female behaviorduring courtship reflects female mate choice, male behaviorcorrelates with male social status, and the male sex pheromoneis the character used by females to assess males. In the presentstudy, males and females were allowed to develop from adultemergence to sexual maturity in either a high- or low-qualityenvironment. The environment affected the quantities of sexpheromone components. We found significantly less 3-hydroxy-2-butanoneand 4-ethyl-2-methoxyphenol, but not 2-methylthiazolidine, inthe pheromone glands of males from a poor environment. Pheromonequality was also affected; the ratios involving 2-methylthiazolidinewere altered, while the ratio 3-hydroxy-2-butanone to 4-ethyl-2-methoxyphenoldid not change. Development to sexual maturity under these environmentalconditions also influenced male and female sexual behavior.Male courtship activity reflected environmental influences;males from the low-quality environment took longer to initiatecourtship and spent more time copulating with females from allenvironments. Male quality, as assessed by females, was alsoaffected by their environment. Females were slower to respondto the courtship of males from the poor environment, regardlessof the females' own rearing environments. However, females fromthe low-quality environment also took longer to respond to thecourtship, and required more courtship, regardless of the males'rearing environments. Thus, poor environments also increasefemale choosiness. However, there was only one significant interactionterm, suggesting that the environmental effects are generaland that females do not show adaptive plasticity in mate choice.Studies of sexual selection that consider the effects of variableenvironments on behavior as well as the sexually selected morphologyin other systems are likely to provide new insights into thisevolutionary process     

The mating behaviour of the seed shrimp Parapolycope spiralis (Ostracoda: Cladocopina), with insight into the evolution of mating systems in cryptic interstitial habitats

The mating behaviour of the interstitial ostracod Parapolycope spiralis Tanaka & Tsukagoshi, 2010 is reported here for the first time. This species is adapted to an interstitial environment, and is typified by having tiny body size and being completely blind. In this paper it is presumed that the characteristics of the mating behaviour are typical for species in an interstitial environment. Observations by microscopy on mating behaviour in the laboratory showed various distinct stages: (1) the male captures the female by a sucker on the antennula; (2) the male clasps and maintains the mating position using the endopodite, the endopodite claw, and the exopodite of the antenna; (3) the male makes contact using the distal part of the upper lip; and (4) copulation takes place. These observations indicate that the sequence of stages of the mating behaviour of miniaturized animals is not necessarily always a simplified process. During the process, it seems that the male upper lip establishes physical contact stimuli with the female. Because the interstitial environment is cryptic and consists of a three‐dimensional space with reduced connectivity, direct physical contact is likely to be one of the most effective and successful courtship behaviours. © 2013 The Linnean Society of London, Biological Journal of the Linnean Society, 2013, 109 , 791–801.     

Optimal traits when there are several costs: the interaction of mortality and energy costs in determining foraging behavior

I analyzed the interaction of different types of costs in determiningoptimal behavior using mathematical models. The analysis concentrateson foraging behavior and asks (1) whether the cost factor thathas the greatest effect on fitness generally has the greatesteffect on optimal trait values and (2) whether increasing thesize of one type of cost makes the optimal behavior absolutelyor relatively more sensitive to that cost. The foraging costsconsidered are energy expenditure, predation risk, and othermortality factors. It is shown that increasing the magnitudeof one cost often decreases the relative and absolute sensitivityof the optimal foraging strategy to that cost. The relativefitness effects of different costs generally differ from therelative sensitivities of the optimal strategies to the costfactors. Researchers should therefore measure the shapes ofcost curves rather than their average magnitudes to determinewhich of several costs can be ignored in cost-benefit analyses.     

The importance of male and female acoustic behaviour for reproductive isolation in Ribautodelphax planthoppers (Homoptera: Delphacidae)

The importance for reproductive isolation of species-specific acoustic differences between closely related Ribautodelphax planthopper species is tested by measuring responses to playbacks of both conspecific and heterospecific signals. Females respond to heterospecific male calls at about 80% of the conspecific response level, irrespective of the degree of cross-insemination of the combination involved. In a combination involving R. albostriatus , a taxonomically more distantly related species, female response levels are only 15–33% of the normal level. Study of the development of both female responsiveness and receptiveness shows that response levels correspond fairly well with insemination levels. Female heterospecific response is far too high to explain isolation between the species. Female answers to heterospecific males calls have normal response-delay times and durations. When offered a two-way choice between female playback calls, males significantly more often approach the conspecific call in almost all combinations tested. Offering only a heterospecific female signal induces males to call, but not to search. Males are capable of maintaining at least part of the sexual isolation by distinguishing between different female calls. This seems in conflict with the popular theory that the sex with the greater parental investment, here the female, should be exerting the choice.     

Courtship in long-legged flies (Diptera: Dolichopodidae): function and evolution of signals

Analyzing the courtship behavior of long-legged flies (Diptera:Dolichopodidae), we focus on the evolutionary development ofcourtship signals. Long-legged flies may serve as a model forthis evolutionary process, because males of some species presentsexually dimorphic badges during courtship, whereas others donot exhibit such conspicuous signals but present lavish courtshipbehavior, including dynamic flight maneuvers. A comparison ofthese two groups within a single taxonomic family provides insightinto the evolution of courtship signals and the correspondingbehavior. Males of the closely related Empididae do not possesssuch badges. Within the super-family Empidoidea, we proposean evolutionary shift from dynamically courting and mating onthe wing (in Empididae) to courting and mating on ground (inDolichopodidae), accompanied by signaling through badge-waving.By comparing previously published data and observations on courtshipbehavior in Dolichopodidae, we present the hypothesis that thelatter replaced the former energetically expensive behavioras a case of automimicry and sensory trap.     

Female greater wax moths reduce sexual display behavior in relation to the potential risk of predation by echolocating bats

Female greater wax moths Galleria mellonella display by wing fanning in response to bursts of ultrasonic calls produced bymales. The temporal and spectral characteristics of these callsshow some similarities with the echolocation calls of batsthat emit frequency-modulated (FM) signals. Female G. mellonellatherefore need to distinguish between the attractive signalsof male conspecifics, which may lead to mating opportunities,and similar sounds made by predatory bats. We therefore predictedthat (1) females would display in response to playbacks of male calls; (2) females would not display in response to playbacksof the calls of echolocating bats (we used the calls of Daubenton'sbat Myotis daubentonii as representative of a typical FM echolocatingbat); and (3) when presented with male calls and bat callsduring the same time block, females would display more whenperceived predation risk was lower. We manipulated predationrisk in two ways. First, we varied the intensity of bat callsto represent a nearby (high risk) or distant (low risk) bat.Second, we played back calls of bats searching for prey (lowrisk) and attacking prey (high risk). All predictions weresupported, suggesting that female G. mellonella are able todistinguish conspecific male mating calls from bat calls, andthat they modify display rate in relation to predation risk.The mechanism (s) by which the moths separate the calls ofbat and moth must involve temporal cues. Bat and moth signalsdiffer considerably in duration, and differences in durationcould be encoded by the moth's nervous system and used in discrimination.     

A test of the risk allocation hypothesis: tadpole responses to temporal change in predation risk

The risk allocation hypothesis predicts that temporal variationin predation risk can influence how animals allocate feedingbehavior among situations that differ in danger. We testedthe risk allocation model with tadpoles of the frog Rana lessonae,which satisfy the main assumptions of this model because theymust feed to reach metamorphosis within a single season, theirbehavioral defense against predators is costly, and they canrespond to changes in risk integrated over time. Our experiment switched tadpoles between artificial ponds with different numbersof caged dragonfly larvae and held them at high and low riskfor different portions of their lives. Tadpoles responded stronglyto predators, but they did not obey the risk allocation hypothesis:as the high-risk environment became more dangerous, there wasno tendency for tadpoles to allocate more feeding to the low-riskenvironment, and as tadpoles spent more time at risk, they didnot increase feeding in both environments. Our results suggestthat the model might be more applicable when the time spentunder high predation risk is large relative to the time requiredto collect resources.     

When to come out from a refuge: risk-sensitive and state-dependent decisions in an alpine lizard

Prey often respond to predator presence by increasing theiruse of refuges. However, unfavorable thermal conditions in refugesmight entail physiological costs for an ectothermic prey. Thus,the decision of when to come out from a refuge should be optimizedby considering the expected fitness effects of diminution ofpredation risk with time, but also by considering the cost of theloss of time spent at optimal body temperature maximizing physiological functions.The model of Ydenberg and Dill describes the trade-off betweenrisk and cost for a prey fleeing to a refuge. We present a specialcase of this model to predict how emergence time from the refugein lizards or other ectotherms should vary as a function ofrisk of predation and thermal costs of refuge use. The analysesof the variation in emergence time from a refuge of Lacertamonticola lizards in the field under two different predation risklevels supported the predictions of the model. As predicted,time spent in the refuge was longer when the threat of the initialattack had been higher, and therefore the subsequent diminutionof risk was slower, but only when lizards emerged at the sameplace where they hid. When initial body temperature was high,some lizards decreased emergence time by emerging from a differentplace. In addition, the effects of thermal costs were more relevant inthe high-risk situation. Time spent in the refuge under highrisk increased when thermal conditions of the refuge were moresimilar to thermal conditions outside (i.e., physiological costsof refuge use were lower). We conclude that optimization ofrefuge-use strategies might help lizards cope with changes in predationrisk without incurring excessive physiological costs.     

Living with the enemy: avoidance of hyenas and lions by cheetahs in the Serengeti

Predator avoidance is likely to play a strong role in structuringspecies communities, even where actual mortality due to predationis low. In such systems, mortality may be low because predatoravoidance is effective, and if the threat of predation is liftedthen entire community structures may be altered. Where competitionis intense, then competitor avoidance may have a similar impacton communities. Avoidance behaviors have been documented fora wide range of species, but this is the first attempt to documentavoidance behavior within a large carnivore community. Audioplayback techniques are used to examine the risk perceivedby cheetahs from their two main competitors that are also theirmain predators, lions and hyenas. The results from these experimentsshow that cheetahs actively moved away from lion and hyenaplayback experiments, compared with dummy playbacks where nosound was played. Cheetahs showed no differences in their responsesto playbacks dependent on their sex or reproductive status,suggesting they were responding principally to a competitionrather than a predation threat. However, cheetahs were muchless likely to hunt after competitor playbacks than after dummyplaybacks, and this resulted in a lower kill rate after competitorplaybacks, demonstrating that the perceived presence of competitorshad a noticeable impact on the foraging rate of cheetahs. Furthermore,while cheetahs moved just as far following lion playbacks asafter hyena playbacks, they spent significantly more time lookingat the loudspeaker and were less likely to make a kill afterlion playbacks, suggesting that cheetahs perceive lions tobe a greater threat than hyenas.     

The kinds of traits involved in male--male competition: a comparison of plumage, behavior, and body size in quail

I compared the role of ornate plumage, behavior, and body sizeduring male—male competition in two species of New Worldquail. Gambel's quail (Callipepla gambelii) is a highly ornateand dichromatic species, whereas scaled quail (C. squamata)is unornamented and monochromatic. During paired contests betweenunfamiliar males, high rates of testosterone-mediated behaviors(tidbitting, calling) and large body size (mass, tarsus, andtail length) corresponded to winners. In the highly ornate Gambel's quail, male head plumes also influenced the outcomeof contests. Plume enhancement made Gambel's quail more likelyto win contests, whereas plume removal made males more likelyto lose. Plume position also reflected male status. Winningmales erected plumes, whereas losers frequently flattened them.Some plumage ornaments, such as belly patches, did not playa primary role during male contests. Unlike static ornaments,head plumes are highly modifiable and likely signal immediateinformation regarding a male's intent, similar to a coverablebadge. Combined, intrasexual selection favored dynamic traits(fast display rates, modifiable ornaments) and static traits(body size) as indicators of male condition or motivation.In scaled quail only, male size was favored both by male—malecompetition and female choice. Accordingly, the degree of sizedimorphism (tarsus length) is greater in scaled than in Gambel'squail. The frequency of overt aggression (chases, pecks, displacement)also differed between species. Gambel's quail were very aggressive,and subordinates often challenged their opponents. In contrast, scaled quail were less aggressive, and subordinates rarely disputedrank. Interspecific comparison indicated differences in themaintenance of male status and possibly in the honesty of signaling.Both appear to be related to differences in social system.