Colonial breeding and nest defence in Montagu's harrier (Circus pygargus)

We assessed whether colonial breeding allows individuals to decrease their investment in predator defence, by presenting decoys of owls, foxes and crows to Montagu's harrier, Circus pygargus. Decoy detection increased with colony size, as did the number of individuals mobbing the decoy. The number of mobbers was greater for predators potentially risky for the adults (owl or fox) than for non-dangerous predators (crow). Recruits (breeding neighbours, fledglings and non-breeders) were present a lower percentage of the time, and attacked and alarm called less frequently than tested individuals. Nevertheless, the overall attack rate on the predator increased with the number of mobbers. When the size of the mobbing group increased, individuals were more likely to attack predators that represented a risk for adults, but did so less intensively and with a lower frequency of close dives. Thus, coloniality decreased the individual costs of defence in terms of risk taken, whilst enhancing defence efficacy. Birds alarm called more intensively when presented with dangerous predators than with the crow. The number of recruits significantly increased with increasing alarm rate of the tested individuals, even when taking colony size into account. Furthermore, the alarm rate of the tested birds also had a significant effect on the proportion of recruits that engaged in attacks against dangerous predators but not against the crow. The higher recruitment and attack rates for dangerous predators were thus apparently modulated through alarm calling. We discuss whether tested birds may manipulate recruits' behaviour to lessen their own risk.     

Snake-directed mobbing by the Formosan squirrel Callosciurus erythraeus thaiwanensis

Summary The Formosan squirrel Callosciurus erythraeus thaiwanensis was often observed mobbing the snake Elaphe climacophora. A total of 36 natural and 21 experimentally induced mobbings were observed and analyzed. The number of attending squirrels per mobbing event varied from one to seven, and 84% of observed mobbings were performed by more than one individual. The duration of a mobbing bout increased directly with the number of assembled mobbers. In 68% of cases, one adult female was one of the mobbers; there was never more than one female per mob. The number of assembled males per mob varied from 0 to 5; 40% of the mobbings involved two or more males. This difference is correlated to a difference in spacing patterns of both sexes; female home ranges were distributed exclusively, whereas male home ranges overlapped each other. Females mated with multiple males whose home ranges overlapped theirs. Female's reproductive status (conception, lactation, and weaning) affected their intensity of response to the playback of mobbing calls, females in pup-rearing period being the most sensitive. One function of the mobbing appears to be defense of the young against snake predation. Females mobbed more intensively and longer than males. Males that had resided at the study site for at least 1 year tended to mob more frequently than intruders.     

Determinants of brood defence in the great tit Parus major L.

Summary Great tits (Parus major) tending nestlings reacted defensively to a live predator (Glaucidium perlatum; domestic cat) and the playback of a mixed species mobbing chorus, or to the latter alone. Defensive behaviour, mainly mobbing, reflected the risk taken and is assessed by five measures. Multivariate and contingency analyses revealed that at least 11 of 16 contextual independent variables affected the risk taken. Incremental effects are due to: Age of young, sex of the defending bird, the expected number of neighbouring mobbers, low temperature, wet canopy, the raptor's distance from cover, coniferous forest, advancing season. A decremental effect is exerted by a large brood that is older. Annual differences in defence arise probably from demographic factors such as fecundity, which in turn affect the parent's benefit-cost ratio (number of young of the same sex as the parent/residual reproductive value of the parent).While the effects of annual fecundity, age of young and season were predicted on the basis of this benefit-cost ratio, the failure to verify an incremental effect of brood size runs counter to established theory. We conclude that parents gear their defence efforts to energy investment, past or future, and are mal-adapted to brood size as a promotor of risk taken. The influence of the habitat is poorly understood. At least three factors (age and number of young, parent's sex) act additively on part of the response. Despite the large number of variables examined, about 43% of the total response variance remains unexplained.While four defence measures are determined by at least 10 contextual factors, a fifth measure, the male's minimum distance from the raptor, is determined by one other factor, the appearance of the male. The latter leads us to assume an additional, social rôle of brood defence.Risk-assessment by great tits leading to risk-aversive defence behaviour is governed by evolved restraints rather than by momentary constraints. Examples are provided by the effects of weather and cover.     

The multidimensionality of behavioural defences against brood parasites: evidence for a behavioural syndrome in magpies?

Studies of antiparasite defences against cuckoo parasites have largely neglected the possibility that behavioural components of host defence may correlate giving rise to a behavioural syndrome. Furthermore, the different contribution of the host’s sex in nest defence has traditionally been disregarded. Here, we studied magpie (Pica pica) mobbing behaviour towards dummies of great spotted cuckoo (Clamator glandarius) and non-harmful hoopoes (Upupa epops) and egg rejection of parasite eggs in a population of colour-banded magpies. We predicted a positive correlation between the intensity of nest defence and egg rejection within each sex and that females respond more intensely than males to the threat of brood parasitism as they undertake incubation. Magpie males, but not females, defended their nests more intensely in those nests in which cuckoo model eggs were rejected. Individual magpies did significantly differ in their baseline level of nest attentiveness; however, there were no individual differences once pair identity was considered. Males and females defended their nests more intensely when it was exposed to the presence of a great spotted cuckoo dummy. Males, but not females, were more prone to appear at their nests, and females, but not males, were more prone to defend more intensely when their nests were challenged by a parasite threat. Our results thus agree with the view that mobbing behaviour and egg rejection in magpies may actually constitute a pseudosyndrome and highlight the necessity to integrate interindividual variation and the sex of the host in studies of the evolution of host defences.     

Chemical polymorphism in male femoral gland secretions matches polymorphic coloration in common wall lizards (Podarcis muralis)

Previous studies showed that common wall lizards (Podarcis muralis) are polymorphic in colour, both sexes showing three main ventral morphs (white, yellow and red) within the same population and that the three morphs correlate with many life-history traits, including a positive assortative mating according to colour. Chemical communication plays a key role in intra-specific recognition and in social organization of lizards; thus chemical cues might be involved in morph recognition and mate choice. We used gas chromatography–mass spectrometry (GC–MS) to investigate possible differences in the lipophilic fraction of femoral gland secretions between size/age classes and to explore whether chemical secretions match male colour morphs. As expected, most males shared the same compounds, but smaller males showed significantly higher proportions of aldehydes, alcohols and ketones and significantly lower proportions of tocopherols than larger males. Interestingly, inter-morph differences in the proportion of some compounds (especially tocopherols and furanones) matched ventral colour polymorphism. Pairwise comparisons showed that white lizards had significantly different chemical profiles than both the yellow and red ones, whereas differences between yellow and red males were only marginal. A further canonical analysis of principal coordinates correctly classified 67.2 % on average of the chemical profiles according to colour morph (white 85.0 %, red 60.9 %, yellow 57.1 %). We hypothesized that chemical differences associated with colour polymorphism may play a central role in intra-specific communication and even in sexual selection, allowing individuals to choose their partners according to their age, and more interestingly according to their colour morph, in a non-random mating population system.     

Melanin-based colour polymorphism signals aggressive personality in nest and territory defence in the tawny owl (Strix aluco)

Nest and territory defence are risky and potentially dangerous behaviours. If the resolution of life history trade-offs differs between individuals, the level of defence may also vary among individuals. Because melanin-based colour traits can be associated with life history strategies, differently coloured individuals may display different nest and territory defence strategies. We investigated this issue in the colour polymorphic tawny owl (Strix aluco) for which plumage varies from dark to light reddish melanic. Accordingly, we found that (1) our presence induced a greater response (flying around) from dark-coloured than light-coloured females and (2) dark reddish males suffered lower nest predation rates than light-coloured males. In experimentally enlarged broods, the probability that females reacted after we played back the hoot calls of a stranger male was higher if these females were lighter reddish; the opposite pattern was found in experimentally reduced broods with dark parents being more reactive than light parents. Finally, darker females alarmed more frequently when paired with a light than with a dark male, suggesting that partners adjust their behaviour to each other. We also tested whether colouration is used as a signal by conspecifics to adjust the level of their defensive behaviour. Accordingly, breeding females responded more vigorously to a dark than a light reddish stuffed tawny owl placed beside their nest. We conclude that melanin-based colouration is a signal of alternative nest and territory defence behaviour that depends on ecological factors.     

The optimal balance of defence investment strategies in clonal colonies of social aphids

Social aphid species provide ideal systems to study the ecological influences upon the evolution of sociality because they consist of discrete colonies which are entirely clonal and therefore devoid of any genetic conflict over altruistic behaviour. Although selfishness can be discounted as an obstacle preventing the evolution of altruistic defenders, the vast majority of aphid species are not social. To examine the key life-history and ecological characteristics that interact to facilitate social evolution, we designed a matrix population model based on the natural history of one of the unique aphid species with soldiers, Pemphigus spyrothecae. In addressing the life-history factors, our special interest was to examine the optimal trade-off faced by colonies that can increase their defence investment by producing defenders at birth and/or increasing the duration of the defensive stage. The level and period of exposure to predation and a declining colony birth rate were key factors that selected for social defence. The model demonstrated that, in species which have soldiers that can facultatively develop to make a direct contribution to colony fitness, temporal extension of the soldier stage is a key mechanism of increasing defence investment. This extension is particularly favoured when predation is high and the lifetime of a colony is long. An increase in production of defenders at birth was favoured when mortality due to predation was strongly biased towards defenders. The model suggests that, in species which have the defensive flexibility of choosing whether soldiers remain as such, there is little requirement for flexibility in the morph allocations made at birth. All these predictions were found to be fully compatible with the available empirical data.     

Territory defence in tropical birds: are females as aggressive as males?

Much of our knowledge concerning the functions of territorial behaviour and how territories are defended by individuals comes from research on birds. The vast majority of this work has focused on temperate zone breeding territoriality in which territories are defended most obviously by males. Our understanding of the female role in territory defence is limited because they are less conspicuous and much harder to observe. We studied sex roles in territory maintenance and defence in a duetting, resident neotropical passerine, the white-bellied antbird (Myrmeciza longipes). This species maintains territories and pair bonds year round and both sexes sing and actively participate in territory defence. We performed a series of playback experiments throughout the dry (non-breeding) and wet (breeding) seasons. We exposed territorial pairs to three types of stimuli including: (1) single sex, male only songs, (2) single sex, female only songs, and (3) both sex songs/duets. Contrary to findings for most other tropical species, individuals defended their territories with equal levels of aggression regardless of stimuli. Furthermore, sex roles were very different, with males responding more aggressively than females to all stimuli throughout both seasons. Both males and females consistently responded more aggressively to territorial intrusions during the dry season than during the wet season, likely because food abundance is low in the dry season and territory value is high. Our analysis of duetting behaviour suggests that duets do not serve a significant role in mate guarding, or territory defence.     

"Mobbing" in Hawaiian Monk Seals (Monachus schauinslani): The Value of Simulation Modeling in the Absence of Apparently Crucial Data

Several small populations of Hawaiian monk seals ( Monachus schauinslani ) exhibit male-biased adult sex ratios and "mobbing," an aggressive behavior in which adult males injure and often kill adult females and immature seals of both sexes during mating attempts. Mobbing appears to be limiting the growth of some populations of this endangered species. The frequency of mobbing deaths appears to increase as a population's sex ratio becomes increasingly male-biased, although the exact relationship between these two variables (the mobbing response) is unknown. We developed a stochastic demographic model of a small Hawaiian monk seal population using several different assumptions about the mobbing response. We used the model to explore the origins of male-biased sex ratios in monk seal populations and to determine whether it was possible, given the lack of data on the mobbing response, to evaluate the probable effects of alternative management strategies to address the mobbing problem. Small populations (100 to 200 seals) and those with slower growth rates were more likely to develop male-biased adult sex ratios. Almost all of our modeling scenarios supported the immediate removal of males from populations where mobbing occurs. Our conclusions were relatively unaffected when the assumptions regarding the mobbing response were varied. Thus, a model was helpful even when apparently crucial data were unavailable.     

Experimental evidence of reciprocal altruism in the pied flycatcher

Although human behaviour abounds with reciprocal altruism, few examples exist documenting reciprocal altruism in animals. Recent non-experimental evidence suggests that reciprocal altruism may be more common in nature than previously documented. Here we present experimental evidence of mobbing behaviour, the joint assault on a predator in an attempt to drive it away, as reciprocal altruism in the breeding pied flycatcher (Ficedula hypoleuca). Given a choice, pied flycatchers assisted in mobbing initiated by co-operating neighbours and did not join in mobbing when initiated by conspecific neighbours which had defected from necessary assistance 1 h before. The results suggest the birds followed a ‘tit-for-tat’-like strategy and that mobbing behaviour of breeding birds may be explained in terms of reciprocal altruism.     

The influence of experience on risk taking: results from a common-garden experiment on populations of Eurasian perch

Predation is often thought of as an unforgiving and strong selective force, quickly selecting against maladaptive behaviour in the prey. It is argued that experience is likely to have low influence on the phenotypic response to predation, as failing to react correctly to a predator may mean death to the prey and no second chance to learn and correct the behaviour. Individuals from different populations of Eurasian perch are known to differ in risk-taking behaviour. Variation in predation pressure has been suggested as a key factor causing these differences, but little is known about the underlying mechanism by which predation generates risk-taking phenotypes in perch. We compared the degree of boldness between two natural populations of Eurasian perch, living under different predation regimes, and the same populations hatched and reared under identical conditions, free from predation. By this common-garden approach, we sought to investigate patterns in the influence of inheritance and experience on boldness phenotype. The wild fish differed in risk taking, with fish from the low predation-risk population acting bolder than fish from the high-risk environment. In the reared fish, both populations behaved equally bold. Only the fish originating from the high predation population showed different behaviour when comparing wild and reared ecotypes. Our results suggest that experience has an important impact on the response to predators and that geographic variation in risk taking between populations of Eurasian perch to a high degree is shaped by adjustments to the current environment. Habituation had an effect of risk-taking behaviour over the experimental period, but consistent differences between individuals were also found. Furthermore, we also show, by the estimation of variance components, that the behaviour we observe is affected by a range of random effects, such as aquaria and group membership, that in concert shapes the behaviour of an individual perch.     

Are blue eggs a sexually selected signal of female collared flycatchers? A cross-fostering experiment

Impressive variation in egg colouration among birds has puzzled evolutionary biologists for a long time. The most frequently studied selective forces moulding egg colouration—predation and brood parasitism—have either received little empirical support or may play a role in only a minority of species. A novel hypothesis has suggested that egg colour may be significantly influenced by sexual selection. Females may deposit a blue-green pigment biliverdin into eggshells instead of using it for themselves as a powerful antioxidant. By this handicap, females may signal their quality to males, which are then hypothesized to increase their paternal effort. We experimentally tested the hypothesis in the collared flycatcher (Ficedula albicollis), a species laying blue-green eggs. We cross-fostered clutches between nests to disentangle effects of female/territory quality and egg colour on paternal effort and nestling quality. The results supported two assumptions of sexual signalling through egg colour hypothesis: Blue pigment seems to be a limited resource for females, and female quality is positively correlated with the intensity of the blue-green colour. However, we did not find support for the main prediction of the hypothesis, as male parental effort parameters (feeding frequencies to nestlings and intensity of nest defence) were unrelated to egg colour. We discuss possible reasons for the discrepancy between our results and previous correlative analyses that supported the hypothesis that blue egg colour may be a postmating, sexually selected signal in females.     

Kill before being killed: an experimental approach supports the predator-removal hypothesis as a determinant of intraguild predation in top predators

Intraguild predation (IGP) has been explained in terms of competitor-removal, food-stress and predator-removal hypotheses. Only the first two hypotheses have been fairly well studied. To test the predator-removal hypothesis as a force determining IGP in avian predators, we performed a field experiment to simulate the presence of an IG predator (eagle owl Bubo bubo dummy) in the surrounding of the nests of four potential IG prey (black kite Milvus migrans, red kite Milvus milvus, booted eagle Aquila pennata and common buzzard Buteo buteo). To discard the possibility that an aggressive reaction towards the eagle owl was not related to the presence of the IG predator, we also presented a stuffed tawny owl Strix aluco, which is a potential competitor but cannot be considered an IG predator of the studied diurnal raptors considered in the experiment. While almost always ignoring the tawny owl, raptors chiefly showed an interspecific aggressive behaviour towards their IG predator. Our results seem to support the predator-removal hypothesis, as the IG prey may take advantage of the diurnal inactivity of the IG predator to remove it from their territory. However, the recorded behaviour may be also considered as a special variety of mobbing (i.e. a prey’s counter-strategy against its predator), where the mobber is sufficiently powerful to escalate predator harassment into deliberate killing attempts. In their turn, eagle owls can respond with an IG predatory behaviour aimed at removing IG prey species which are highly aggressive mobbers.     

A dynamic trait affects continuous pair assessment in the blue-footed booby,<Emphasis Type="Italic"> Sula nebouxii</Emphasis>

Bright colours of male birds have often been shown to be the target of sexual selection through female choice, yet few studies have looked at the role of colour expressed after pairing on female motivation and behaviour. Here we analyse the role of an integumentary colour in the spectral range of 400–700 nm, the foot colour in male blue-footed boobies, Sula nebouxii, which is prominently displayed during pair courtship. Measurements early in the breeding season showed that foot colour of courting males is pale (high values of brightness) and has an aqua-blue chroma, and females in better body condition were mated to males with brighter feet. We carried out an experimental manipulation which modified the foot colour of males in courtship, making it closer to the foot colour of males in low nutritional state. We found that females paired to experimental males courted less and were less likely to copulate than females in the control group. Male behaviour was apparently unaffected by the manipulation; thus the change in female behaviour can be attributed exclusively to foot colour manipulation. These results strongly support the hypothesis of female preference for an integumentary colour and suggest that this dynamic trait is used as a male ornament after pairing.Communicated by J. Graves     

Alternative male mating tactics in a cichlid, Pelvicachromis pulcher: a comparison of reproductive effort and success

Pelvicachromis pulcher is a small African cichlid which breeds in holes. Males may either reproduce monogamously (pair males), polygynously (harem males), or be tolerated as helpers in a harem territory (satellite males). These helpers share in defence of the territory against conspecifics, heterospecific competitors and predators. There are two male colour morphs that are fixed for life and are apparently genetically determined. These differ in their potential mating strategy. Red morph males may become harem owners, while yellow morph males may become satellite males, and males of both morphs may alternatively pair up monogamously. We compared the reproductive effort and success of these three male reproductive strategies. Effort was measured as attack rates, time expenditure and the risk of being injured or killed when attacking competitors or predators of three sympatric fish species. Reproductive success was measured by observing how many eggs were fertilized by each male when this was possible, and by using genetic markers. The number of fry surviving to independence of parental care was used as a criterion of success. The reproductive success of harem males was 3.3 times higher than that of pair males and 7 times higher than that of the average satellite male. Dominant satellite males, however, were as successful as monogamous pair males, using the measure of fertilized eggs. To our knowledge, this has not been found previously in any fish species. Both harem and pair males had lower parental defence costs per sired offspring, however, than males using the alternative satellite tactic. Defence effort was significantly related to the risk of injury. Received: 17 January 1996 / Accepted after revision: 9 June 1997     

Brood defence in the great tit (Parus major): the influence of life-history and habitat

Summary We examined the extent to which parental investment, as measured by brood defence, is determined by life-historical selection in a shortlived bird, the great tit (Parus major). Pairs tending first (n=20) and second (n=21) broods in the same Scots pine woods in 1983 were used to test predictions of a cost/benefit model of brood defence based on the species' average demography in coniferous forest. Furthermore, the differences in demography between pine and deciduous forest permitted us to test whether habitat-specific life-history would affect the seasonal pattern of defence. In the model, benefit was defined as the brood's potential contribution to a parent's fitness, and the cost as the potential loss if the defender dies in the act of defence. Univariate and multivariate procedures were applied to six measures of defence response to a live owl (Glaucidium perlatum) plus a taped mobbing chorus. Results proved three of the model's predictions to be false. In coniferous forest, neither the overall strength nor the individual variance of defence behaviour differed among first and second broods, nor was there any consistent difference in defence strength between pairs living in coniferous (n=54) or deciduous (n=84) forest as revealed by comparisons within each brood. These failures could be reconciled with the model by assuming that selection in the past had acted via the average demography of both types of habitat. The model received direct support from defence strength increasing with age of young and, more forcefully, becoming more influenced by brood size in second broods, regardless of habitat.A difference in the strength of defence by the male and female suggests two more functions of behaviour: In first broods, the male risks more than the female as measured by five of six variables. This suggests that defence is facultatively linked to the need for territorial protection from predators all the year round. In the female's presence, the male, taking an additional risk, approaches the owl to half the distance of that of a single, though paired, male, suggesting an additional, social role of defence behaviour.Taken together, anti-predator defence in the great tit serves to protect the brood, the home range and, in the male, the female mate. The magnitude of the benefits envisaged varies among the sexes.     

Social,environmental and genetic factors in the ontogeny of phenotypic differentiation in a lizard with alternative male reproductive strategies

Summary Adult male tree lizards, Urosaurus ornatus, practise alternative (territorial or sneaker/satellite) reproductive strategies that are correlated with differences in throat color and body size. In this study we raised tree lizards from hatching in the laboratory to examine the question of whether the phenotypic expression of secondary sex coloration and body size can be facultatively influenced by social or abiotic environmental factors. We compared males reared in the laboratory under different social and environmental conditions to males in the field and found no effect of different conditions on phenotypic differentiation (Figs. 2–4). Thus, phenotypic differences between morphs probably result largely from nonfacultative expression of different genotypes. This suggests that alternative male morphs practise a mixed evolutionary stable strategy (ESS) rather than one morph making the best of a bad situation. However, in the context of ESS theory it is difficult to explain our further result that the nonterritorial morph in this species grows faster and reaches a larger adult body size than the territorial morph (Fig. 5).     

Duetting in the subdesert mesite Monias benschi: evidence for acoustic mate defence?

Despite numerous hypotheses proposed for the function of duets, there is currently no consensus as to why males and females should coordinate their songs in such a precise way. There is evidence indicating that duets sometimes serve in territory defence, but additional functions are rarely considered. The mate-defence hypothesis proposes that birds sing in response to their partner's song and the resulting duet repels rivals and may prevent desertion of a partner. We investigated this idea in the subdesert mesite Monias benschi using playback experiments in which we broadcast recordings of solos and duets to single birds and groups. Two predictions of the hypothesis were met: (1) the solo songs of both sexes incited aggressive responses from paired birds of the same sex; and (2) compared to solo songs, pair duets elicited weaker responses from groups and duetting pairs. However, groups responded to male duets with a vigour equal to that with which they responded to male solos. This indicated that the weaker responses of groups to pair duets compared to male solos was a function of the sex rather than number of vocalising birds. Groups responded more strongly to male solos than to either female solos or pair duets, and females' responses were generally weaker than those of males. This may reflect stronger competition among males for mates, due to a male-biased sex ratio in the population. We conclude that song serves similar functions in each sex and that duets may arise through mutual mate defence.     

Female siskins choose mates by the size of the yellow wing stripe

Commonly, female birds use the brightly coloured patches on males to choose the best-quality mates. Coloured wing patches, however, have received little attention or have been previously related to social behaviour (as a signal to recruit conspecific individuals at feeding patches) or foraging (to flush prey) contexts, rather than to sexual selection. Here we provide evidence that in siskins (Carduelis spinus), wing patches function in mate choice. Mate-choice experiments showed that females were attracted by the size of the yellow wing stripe of the male, but not by the size of its black bib, body size, general plumage brightness or age. Experiments on birds with manipulated yellow wing stripes showed that females were sensitive to the size of this colour patch, irrespective of other male qualities. The preference of female siskins for males with larger wing patches when searching for a mate may be explained by the relationship of this trait to foraging ability, which would ensure females good parental investment from the chosen male.Communicated by W.A. Searcy     

Tests of the harassment-reduction function and frequency-dependent maintenance of a female-specific color polymorphism in a damselfly

Color polymorphisms have provided classical examples of how frequency-dependent selection maintains genetic variation in natural populations. Here we tested for the first time, the hypothesized adaptive function of a female-specific color polymorphism in odonates to lower male harassment towards females generally. Under conditions controlling for sex ratio, population density and morph frequency, we also tested two major frequency-dependent selection hypotheses for the maintenance of the polymorphism. Using groups of captive Enallagma hageni, whose females are either green or a male-like blue, we varied morph frequency at two sex ratios. We quantified sexual harassment towards females by visual observations, and by the presence of dust on females that was transferred from dusted males. Per capita harassment rate for the female-monomorphic treatments did not differ from that of the female-polymorphic treatments. At a male-biased sex ratio, per capita harassment rate towards blue, but not green females increased with morph frequency, providing partial support for frequency-dependent selection resulting from male learning of female morphs. Even at high frequency, green females were not harassed more than blue, contrary to the prediction that males should always recognize green females as mates. Moreover, frequency-dependent harassment towards blue females was not detectable using harassment measured with dust evidence, which greatly underestimated the incidence of sexual harassment. Our findings identified problems with the use of insectaries and the dusting technique to quantify male sexual harassment towards females, as well as with a past insectary experiment on Ischnura elegans that failed to demonstrate frequency-dependent harassment.