Behaviour of a specialist parasitoid, Cotesia melitaearum: from individual behaviour to metapopulation processes

Abstract. 1. Foraging behaviour and movement within and among host patches of the specialist parasitoid wasp Cotesia melitaearum (Braconidae) attacking the larvae of Melitaea cinxia (Nymphalidae) were studied in the field and in the laboratory.
2. In the field, female wasps aggregated in large host groups in the autumn and caused positive spatial density-dependent parasitism in the field. Wasps stayed longer with groups of pre-diapause caterpillars than with post-diapause caterpillars, but attacked them less frequently.
3. In the laboratory, wasps attacked larger larvae more readily than smaller larvae. Also in the laboratory, wasps exposed to larvae outside their protective webs showed differences in the rates at which they attacked larvae fed different diets, implicating host plant-derived chemicals as proximate cues for foraging wasps.
4. Mark–recapture studies indicated that there was a low rate of successful movement of wasps among groups of young larvae within a habitat patch in the autumn and no successful movement of wasps across non-habitat. In contrast, wasps moved frequently among groups of late-instar caterpillars in the spring.
5. Host caterpillars of different ages responded very differently to wasp attacks. Pre-diapause larvae remained in groups and used collective head-jerking behaviour to defend themselves, whereas post-diapause larvae dispersed away from the group immediately after being attacked.
6. Population and metapopulation level dynamics of the host–parasitoid interaction are discussed in light of these observations of the behaviour of individual wasps.     

To mate or not to mate,and subsequent host search by a haplodiploid female parasitoid wasp

Mated females of haplodiploid species can vary the sex ratio of their offspring, but virgin or sperm‐depleted females can produce only males. Depending on the costs and benefits, the theory of constrained sex allocation states that female haplodiploids may vary in their propensity to mate, with important implications for the populations’ sex ratio. Unmated female parasitoid wasps Alabagrus texanus (Braconidae) have been observed to reject matings with males, even under highly confined spatial conditions. We performed field trials to determine whether unmated female A. texanus would mate. We then compared the preferences of the resulting unmated (constrained) and mated (unconstrained) female wasps for shelters constructed and occupied by their hosts, fern moth caterpillars Herpetogramma theseusalis (Crambidae) on fern fronds. We presented the wasps with pairs of shelters collected from the field that differed in size, as well as freshness, fern species, and presence or absence of caterpillars. Unconstrained females searched small shelters more frequently than did constrained females and tended to favor senesced (old) shelters over fresher ones. They did not differ in choice between shelters on marsh and sensitive ferns or between shelters containing caterpillars and empty shelters. The preference for small shelters by the unconstrained wasps may enhance their rate of contacting favorable hosts, but the foraging regime of the constrained females should expose them to caterpillars at sites infrequently searched by the unconstrained females.     

Influence of aphid size,age and behaviour on host choice by the parasitoid wasp Ephedrus californicus: a test of host-size models

Summary When host quality varies, parasitoid wasps are expected to oviposit selectively in high-quality hosts. We tested the assumption underlying host-size models that, for solitary species of wasps, quality is based on host size. Using Ephedrus californicus, a solitary endoparasitoid of the pea aphid, we evaluated the influence of aphid size (= mass), age and defensive behaviours on host selection. Experienced parasitoid females were given a choice among three classes of 5-day-old apterous nymphs: small aphids that had been starved daily for 4 h (S4) and 6 h (S6) respectively, and large aphids permitted to feed (F) normally. Wasps attacked more, and laid more eggs in, small than large aphids (S6>S4>F). This rank-order for attack did not change when females could choose among aphids of the same size that differed in age; however, wasps oviposited in all attacked aphids with equal probability. Host size did not influence parasitoid attack rates when aphids were anaesthetized so that they could not escape or defend themselves. As predicted by host-size models, wasp size increased with host size (F>S4; S6), but large wasps required longer to complete development than their smaller counterparts (S4E. californicus reflects a trade-off between maximization of fitness gains per egg and the economics of search-time allocation. Because large aphids are more likely to escape parasitization, a wasp must balance her potential gain in fitness by ovipositinng in a high-quality (large) aphid against her potential cost in terms of lost opportunity time if the attack fails.     

Direct and indirect effects of predatory wasps (Polistes sp.: Vespidae) on gregarious caterpillars (Hemileuca lucina: Saturniidae)

Summary We examined how predation by vespid wasps,Polistes dominulus andP. fuscatus, affected the behavior, growth rate and survivorship of aggregated caterpillars ofHemileuca lucina (Saturniidae). Although these larvae can exhibit a variety of defense and escape behaviors, in general larvae reacted to wasp attacks by clinging to the hostplant. Neighboring larvae in the aggregation responded by leaving the feeding site and moving to the interior or base of the plant. To determine wheter wasp attack affected the behavior and growth of the caterpillars that escaped, a field experiment was conducted with treatments of: 1) larvae exposed to wasps, 2) larvae protected from wasps, and 3) larvae protected from wasps but with the attack of wasps simulated (=harassment). Over just one instar, protected larvae gained significantly more weight than the harassed larvae, which in turn weighed significantly more than the larvae that escaped the wasps. The behavior of attacked and harassed larvae differed from that of the protected larvae; the disturbed larvae often fed in smaller groups and in shaded portions of the plant where only mature leaves were available. A laboratory experiment showed that at 35° C (daytime temperature) larvae had significantly higher relative growth rates and significantly shorter instar duration than larvae reared at 25° C. Our results suggest that wasps, in addition to killing caterpillars, indirectly affect larval fitness by slowing larval growth, at least in part by forcing larvae into cooler microhabitats where leaves are of lower quality.     

Body size in a pollinating fig wasp and implications for stability in a fig‐pollinator mutualism

The fig–fig pollinator association is a classic case of an obligate mutualism. Fig‐pollinating wasps often have to fly long distances from their natal syconia to a receptive syconium and then must enter the narrow ostiole of the syconium to reproduce. Large wasps are expected to have a greater chance of reaching a receptive syconium. In this study, we tested this hypothesis and then examined whether the ostiole selectively prevented larger pollinators from entering the syconial cavity. In Xishuangbanna, China, Ceratosolen solmsi marchali Mayr (Hymenoptera: Agaonidae) pollinates the dioecious syconia of Ficus hispida L. (Moraceae). The body size of newly emerged wasps and wasps arriving at receptive syconia were compared. Wasps arriving at receptive syconia were significantly larger than newly emerged wasps. We also compared the size of wasps trapped in the ostiole with those in the cavity. Wasps trapped in the ostiole were significantly larger than those in the syconial cavity. Thus, in the case of F. hispida, large wasps were more likely to reach receptive syconia, but the ostiole limited maximum fig wasp size. This indicates that the ostiole, as a selective filter to pollinators, stabilizes pollinator size. Hence, it helps to maintain stability in the fig–fig pollinator mutualism.     

The effect of host developmental stage at parasitism on sex‐related size differentiation in a larval endoparasitoid

• 1 For their larval development, parasitoids depend on the quality and quantity of resources provided by a single host. Therefore, a close relationship is predicted between the size of the host at parasitism and the size of the emerging adult wasp. This relationship is less clear for koinobiont than for idiobiont parasitoids.
• 2 As size differentiation in host species exhibiting sexual size dimorphism (SSD) is likely to occur already during larval development, in koinobiont larval endoparasitoids the size of the emerging adult may also be constrained based on the sex of the host caterpillar.
• 3 Sex‐specific growth trajectories were compared in unparasitised Plutella xylostella caterpillars and in second and fourth instar hosts that were parasitised by the solitary larval koinobiont endoparasitoid Diadegma semiclausum. Both species exhibit SSD, where females are significantly larger than males.
• 4 Healthy female P. xylostella caterpillars developed significantly faster than their male conspecifics. Host regulation induced by D. semiclausum parasitism depended on the instar attacked. Parasitism in second‐instar caterpillars reduced growth compared to healthy unparasitised caterpillars, whereas parasitism in fourth‐instar caterpillars arrested development. The reduction in growth was most pronounced in hosts producing male D. semiclausum.
• 5 Parasitism itself had the largest impact on host growth. SSD in the parasitoid is mainly the result of differences in growth rate of the parasitoid–host complex producing male and female wasps and differences in exploitation of the host resources. Female wasps converted host biomass more efficiently into adult biomass than males.

     

Group hunting by workers of two Neotropical swarm-founding paper wasps, Parachartergus apicalis and Agelaia sp.

Here we report field observations of group hunting by two Neotropical species of paper wasps, Parachartergus apicalis in Costa Rica and Agelaia cf. angulata in Peru. In both cases, multiple workers simultaneously attacked live caterpillar prey. We describe the wasps’ behavior and their interactions with the relatively large-bodied (>80 mm length) caterpillars, and we discuss the implications of these observations for paper wasp behavior and ecology.     

Does Manipulation by the Parasitoid Wasp Cotesia glomerata (L.) Cause Attachment Behaviour of Host Caterpillars on Cocoon Clusters?

Some parasitoid wasps appear to control the behaviour of their hosts. However, altered behaviours of parasitised hosts are not necessarily caused by parasitoids but are sometimes the result of traumatic side effects of parasitism. However, it was difficult for us to discriminate the cause of host's behaviours between manipulation by parasitoids and traumatic side effects. Larvae of the parasitoid wasp Cotesia glomerata form cocoon clusters after egression from the parasitised host caterpillar Pieris brassicae . Following parasitoid egression, host caterpillars survive for several days and remain near the cocoon clusters. These caterpillars may repel solitary pteromalid hyperparasitoid wasps, Trichomalopsis apanteloctena , that attempt to parasitise fresh C. glomerata pupae. We allowed hyperparasitoids to attack cocoon clusters in the field and laboratory and then assessed the costs and benefits to C. glomerata of attachment by the parasitised caterpillars. The eclosion success of C. glomerata in cocoon clusters with attached caterpillars was higher than that in clusters without attached caterpillars in both field and laboratory experiments. This difference was attributed to shorter hyperparasitoid visits to cocoon clusters with attached host caterpillars. However, large cluster size was potentially costly for host attachment, because the duration of host caterpillar attachment decreased with increasing numbers of C. glomerata per caterpillar. This trade-off may be related to shortages of fat body resources, which are shared between the development of wasp larvae and the survival of host caterpillars. Therefore, we concluded that caterpillar attachment satisfied some requirements of host manipulation by C. glomerata .     

Restructuring of Lepidoptera communities by introduced Vespula wasps in a New Zealand beech forest

Introduced social wasps (Vespula vulgaris) reach high densities in some New Zealand beech forests, because honeydew provides an abundant high-energy food source. We manipulated wasp density to estimate an “ecological damage threshold” for large, free-living Lepidoptera larvae. There will be a continuum of ecological damage thresholds for wasp density depending on the prey species or habitat. Experimentally placed small caterpillars had a significantly higher survival rate than large caterpillars, and the survival rate of both groups decreased with increasing wasp density. Spring-occurring caterpillars have a probability of surviving of 0.90–0.95, assuming wasps are the only source of mortality. However, at the peak of the wasp season we predict caterpillars would have virtually no chance (probability of 10⁻⁷⁸ to 10⁻⁴⁰) of surviving to adults. Wasp abundance must be reduced by at least 88% to conserve the more vulnerable species of free-living caterpillars at wasp densities similar to those observed in our study sites. This equates to a damage threshold of 2.7 wasps per Malaise trap per day. It was exceeded for about 5 months of the year in non-poisoned sites. There are currently no biological or chemical control techniques available in New Zealand that will reduce wasp abundance below this damage threshold throughout the year. Our models show that most Lepidoptera with spring caterpillars will be able to persist, but species with caterpillars occurring in the peak wasp season will be eliminated. Received: 5 January 1998 / Accepted: 10 February 1999     

Predatory wasps learn to overcome the shelter defences of their larval prey

Larvae of Epargyreus clarus (Hesperiidae), the silver-spotted skipper, inhabit leaf-and-silk shelters that they construct on their leguminous host plants. In the field, Polistes spp. (Vespidae) wasps land on the shelters, quickly extracting and killing the larvae within. In marked contrast, wasps that emerge from field-collected colonies maintained in the laboratory visit and examine leaflets bearing sheltered caterpillars, but only rarely do they extract and kill the sheltered larvae. To examine whether learning is involved in the development of the ability of Polistes wasps to forage successfully on sheltered E. clarus larvae, we tested the responses of P. fuscatus and P. dominulus wasps to sheltered E. clarus larvae before and after their exposure to unsheltered larvae that were visible either on an opened host-leaf shelter (P. fuscatus and P. dominulus) or on a nonhost leaf in the absence of a shelter (P. fuscatus). After killing and processing an unsheltered larva that was visible on an opened leaf shelter, a majority of foragers subsequently extracted and killed larvae from closed shelters. Wasps that killed and processed an unsheltered larva on a nonhost leaf, on the other hand, generally did not later open shelters. Thus, it seems that experience with an exposed larva in the context of its shelter is necessary for a wasp to be able to prey on sheltered larvae. We conclude that the wasps must learn to associate the taste of the larva with shelter-related cues, such as presence of leaf damage and silk. In nature, this initial exposure may occur when the larva is visible in or near its shelter, perhaps when feeding or constructing a new shelter. Learning opportunities will thus depend on larval density. Our results show that invertebrate predators can learn to overcome their prey's defences, and are therefore able to make use of previously inaccessible prey.     

Uncoupling physical and chemical cues: The independent roles of scale cover size and kairomone concentration on host selection byAphytis melinus DeBach (Hymenoptera: Aphelinidae)

The ectoparasitoidAphytis melinus initially selects its host, California red scale,Aonidiella aurantii (Maskell) (Homoptera: Diaspididae), using characteristics of the host’s cover before assessing the quality of the scale body beneath. Host suitability is known to increase with host size until the scale insect reaches maturity, after which it is no longer available for parasitism. The wasp uses a combination of scale cover size and a kairomone,O-caffeoyltyrosine, in the cover for initial assessment. Under natural conditions these two factors are frequently coupled. We quantified the relative importance of cover size and kairomone concentration independently by removing and selectively reapplying controlled doses of syntheticO-caffeoyltyrosine to scale covers of known size. In the absence of the kairomone, wasps did not discriminate among scale covers differing in size. Wasps showed a curvilinear response to kairomone dose for each scale cover age group. Wasps preferred low doses ofO-caffeoyltyrosine on young, small scale covers, and high doses on old, large scale covers. The ability of wasps to respond quantitatively to the kairomone may be used in the field to differentiate small second-instar from larger and more suitable third-instar scale insect larvae.     

Nest-site size as a short-term constraint on the reproductive success of paternal fishes

Synopsis Because female signal blennies, Emblemaria hypacanthus (Pisces: Chaenopsidae), exhibited a preference for the larger of two males in laboratory mate-choice experiments, male reproductive success was predicted to be positively correlated with male size in field populations. This prediction was met at one field site, but not a second where shelter size, rather than male size, was the primary correlate of male reproductive success. This finding appeared to be the consequence of the relatively small size of shelters (vacant gastropod shells) at the second site. At this site, significantly more males had their shelters filled with eggs and variance in male reproductive success was lower than at the first site. Limited area for deposition of eggs is potentially an important constraint on the short-term reproductive success of paternal males of shelter- or crevice-spawning fishes.     

A chalcid wasp acts chiefly as a hyperparasitoid by mostly using small uncommon hosts

Although ovipositing insects may predominantly use resources that lead to high offspring quality, exceptions to this rule have considerably aided understanding of oviposition decisions. We report the frequency of host species use by a solitary facultative hyperparasitoid, Brachymeria subrugosa Blanchard (Hymenoptera: Chalcididae). In our samples, the wasp attacks the large pupae of the moth Gonioterma indecora Zeller (Lepidoptera: Elachistidae), as well as the considerably smaller, and rarer, pupae of two of its other parasitoids. Consistent with conditional sex allocation models, the wasp produced mainly female offspring on the largest (moth) host, an unbiased sex ratio on the middle‐sized (parasitoid) host, and only males on the smallest (parasitoid) host. Adult offspring size was correlated with the size of the host attacked. These features strongly suggest that the two smaller, primary parasitoid, hosts produce lower‐quality offspring. Despite being more common, the proportion of hosts from which parasitoids emerged was lowest (14%) on the largest host species, and highest on the rarer middle‐sized (34%) and smallest (30%) hosts. This suggests that costs or constraints on attacking high‐quality primary hosts may be a selective force favouring the evolution of hyperparasitism.     

Latitudinal variation in the phenological responses of eastern tent caterpillars and their egg parasitoids

1. Eastern tent caterpillars (Malacosoma americanum) are broadly distributed within North America, with populations spanning a wide range of environmental conditions. Their egg masses are consistently attacked by a variety of wasps in the superfamily Chalcidoidea. We performed a reciprocal transplant‐type experiment to assess the performance of three populations spanning 15° of latitude when subjected to temperature regimes resembling southern or northern conditions. 2. Exposure to warm temperatures and short overwintering periods (southern conditions) resulted in the increased survival of both caterpillars and parasitoids from all populations. By contrast, the ability of caterpillars to withstand starvation was maximised when exposed to conditions similar to their native region. 3. Caterpillar and wasp phenology differed among populations even when exposed to the same temperature regime. Individuals exposed to novel conditions hatched 2–6 weeks later than those experiencing native conditions. Under typical conditions, the relative phenology of wasps and their hosts exhibited a latitudinal gradient consistent with growing season length, with southern, central, and northern wasps, emerging 50, 45, and 36 days, respectively, after their hosts. 3. We identified four genera of primary parasitoids, which emerged within a narrow 2‐week span, and one hyperparasitoid, which emerged in distinct pulses over an approximately 5‐week span, possibly indicating the presence of a second generation. 4. Caterpillars and wasps exhibited distinct phenological responses according to population of origin, indicating that not only pre‐hatching winter and spring conditions, but also historical factors, which may include local adaptation, maternal effects, and oviposition time, influence their phenological responses.     

Cascading effects of host size and host plant species on parasitoid resource allocation

1. The bottom‐up factors that determine parasitoid host use are an important area of research in insect ecology. Host size is likely to be a primary cue for foraging parasitoids due to its potential influence on offspring development time, the risk of multiparasitism, and host immunocompetence. Host size is mediated in part by host‐plant traits that influence herbivore growth and potentially affect a herbivore's quality as a host for parasitoids. 2. Here, we tested how caterpillar host size and host plant species influence adult fly parasitoid size and whether host size influences wasp parasitoid sex allocation. We measured the hind tibia lengths and determined the sex of wasp and fly parasitoids reared from 11 common host species of polyphagous caterpillars (Limacodidae) that were in turn reared on foliage of seven different host plant species. 3. We also tested how host caterpillar species, host caterpillar size, and host and parasitoid phenology affect how the parasitoid community partitions host resources. We found evidence that parasitoids primarily partition their shared hosts based on size, but not by host species or phenology. One index of specialisation (d′) supports our observation that these parasitoids are quite generalised within the Limacodidae. In general, wasps were reared from caterpillars collected in early instars, while flies were reared from caterpillars collected in late instars. Furthermore, for at least one species of solitary wasp, host size influenced sex allocation of offspring by ovipositing females. 4. Host‐plant quality indirectly affected the size attained by a tachinid fly parasitoid through its direct effects on the size and performance of the caterpillar host. The host plants that resulted in the highest caterpillar host performance in the absence of enemies also yielded the largest parasitoid flies, which suggests that host plant quality can cascade up to influence the third trophic level.     

Wasp Attacks and Spider Defence in the Orb Weaving Species <Emphasis Type="Italic">Zygiella x-notata</Emphasis>

Predator–prey relationships are generally based on arm-race. Wasps and spiders are both predators, which could be potential prey for each other. The orb weaver spider Zygiella x-notata is sometimes a prey for the wasp Vespula germanica. We observed the wasp hunting behaviour under natural conditions, and we tested the influence of the spider’s behaviour on the wasp attack success. Wasps were active predators during the reproductive period of the spider. Results showed that wasps located more easily male spiders than females particularly when they were engaged in mate guarding. Female location depended on the presence of a web, but also of prey or prey remains in the web. On the other hand, their location depend neither on the characteristics and the position of the retreat in the environment nor on the size of the web. After location, males were more often captured than females whatever their behaviour (mate guarding or not). Presence of prey remains or prey in the web did not increase the risk for the spider to be captured. There was also no influence of the retreat’s characteristics or of its position in the habitat on the risk for the spider to be captured; but wasp successful attacks were less numerous when silk was present around the entrance of the retreat or when the spider was completely inside. As prey and prey remains favoured location of spiders by the wasps, we tested spider web cleaning behaviour as a response to wasp predatory pressure. By throwing small polystyrene pellets in the webs, we observed that more 80% of the spiders rejected the pellets in less than one minute. Our data indicated that wasps were significant predators of Z. x-notata and wasp attack could have been a selective pressure that had favoured spider defensive behaviours such as web cleaning.     

Effects of prey quantity and quality on predatory wasps

1. The simultaneous effects of prey quantity and prey quality on fitness correlates of the predatory wasp Polistes fuscatus were examined in a glasshouse study. Prey quantity was manipulated by providing prey in excess (high quantity) or one‐third of that (low quantity). Prey quality was manipulated by providing either palatable (Manduca sexta) caterpillars or unpalatable (Junonia coenia) caterpillars. 2. The effect of prey quality on wasp production depended on prey quantity. Nests given unpalatable prey produced few wasps whereas nests given palatable prey increased wasp production with increased prey. 3. The low production of nests given unpalatable prey reflected the low acceptability of those prey. The wasps preferred the palatable prey and learned to reject the unpalatable prey. With no choice of prey, they took only enough unpalatable prey to develop a small nest or colony. 4. A diet of unpalatable prey also resulted in smaller wasps and reduced the proportion of males produced, from about 40% to just 8–14%, depending on the year.     

Sublethal effect of brood parasitism on the grass-carrying wasp Isodontia mexicana

Abstract.  1. The nests of solitary, nest-provisioning wasps (Sphecidae and Crabronidae) are commonly attacked by brood parasites, including flies of the families Phoridae and Sarcophagidae. Larvae of the flies commonly kill the wasp offspring directly or starve it by consuming prey provided by the adult female wasps.
2. To determine whether brood parasitic flies can have a sublethal effect (i.e. reduced body size) on wasp offspring, nests of the wasp Isodontia mexicana were collected at two field sites in upstate New York, U.S.A. Nest diameter had no effect on the probability that a wasp cell would be inhabited by a brood parasite. Most offspring that developed in cells also containing phorids or sarcophagids managed to complete development and emerge as adults. Nevertheless, they had significantly smaller body size than conspecifics emerging from unparasitised cells in which the developing wasp did not have to compete for food (which in this species consists of tree crickets and katydids). Apparently, this is the first time that a sublethal effect of brood parasitism on offspring body size has been quantified for a solitary wasp species. Known effects of body size on the reproductive success of adult wasps suggest that sublethal consequences of the presence of brood parasites may have a significant effect on the fitness of adult I. mexicana .     

Ecological consequences of shelter sharing by leaf-tying caterpillars

A wide variety of insect herbivores construct and inhabit leaf shelters (ties, rolls, folds, and webs). Shelter construction can lead to a high rate of secondary occupation by other arthropods, including other species of constructors. The consequences for the inhabitants of secondarily occupying these shelters are currently unknown. In this study, we conducted field experiments to examine the fitness consequences (survival and attack by natural enemies) for caterpillars that (i) occupy a shelter with conspecifics vs. occur singly; and (ii) establish a new shelter vs. colonize a pre‐existing one. In addition, we conducted factorial laboratory experiments to test the hypothesis that caterpillars sharing shelters with conspecifics might have reduced construction costs (a potential benefit of shelter‐sharing or secondary occupation). Larvae of Psilocorsis quercicella Clemens (Lepidoptera: Oecophoridae) placed in white oak [Quercus alba L. (Fagaceae)] leaf ties alone or in groups of three had equal likelihood of survival from natural enemies. This same caterpillar species, however, had a higher disappearance rate when placed in pre‐existing leaf ties than when placed in newly formed ones, suggesting a potential cost of secondary colonization. A similar experiment with a closely related species [Psilocorsis cryptolechiella (Chambers)], however, failed to detect a cost of secondarily occupying shelters made on beech, Fagus grandifolia Ehrh. (Fagaceae). In the laboratory experiment, we found no evidence of shelter‐sharing benefits; rather larvae reared in shelters in groups of three had lower pupal mass (and thus lower potential fecundity) than larvae reared singly, suggesting a cost of shelter sharing. Moreover, groups of larvae forced to repeatedly construct new shelters tended to have reduced survival relative to the other treatment, suggesting that energetic constraints are more likely to reduce fitness when larvae cohabit shelters. Taken together, these results indicate that the common phenomenon of shelter sharing by leaf‐tying caterpillars has either neutral or negative effects for the occupants. The fact that these leaf‐tying caterpillars actually share shelters may simply reflect limited availability of oviposition sites.     

Strike Fast,Strike Hard: The Red-Throated Caracara Exploits Absconding Behavior of Social Wasps during Nest Predation

Red-throated Caracaras Ibycter americanus (Falconidae) are specialist predators of social wasps in the Neotropics. It had been proposed that these caracaras possess chemical repellents that allow them to take the brood of wasp nests without being attacked by worker wasps. To determine how caracaras exploit nests of social wasps and whether chemical repellents facilitate predation, we: (1) video recorded the birds attacking wasp nests; (2) analyzed surface extracts of the birds'' faces, feet, and feathers for potential chemical repellents; and (3) inflicted mechanical damage on wasp nests to determine the defensive behavior of wasps in response to varying levels of disturbance. During caracara predation events, two species of large-bodied wasps mounted stinging attacks on caracaras, whereas three smaller-bodied wasp species did not. The “hit-and-run” predation tactic of caracaras when they attacked nests of large and aggressive wasps reduced the risk of getting stung. Our data reveal that the predation strategy of caracaras is based on mechanical disturbance of, and damage to, target wasp nests. Caracara attacks and severe experimental disturbance of nests invariably caused wasps to abscond (abandon their nests). Two compounds in caracara foot extracts [sulcatone and iridodial] elicited electrophysiological responses from wasp antennae, and were also present in defensive secretions of sympatric arboreal-nesting Azteca ants. These compounds appear not to be wasp repellents but to be acquired coincidentally by caracaras when they perch on trees inhabited with Azteca ants. We conclude that caracara predation success does not depend on wasp repellents but relies on the absconding response that is typical of swarm-founding polistine wasps. Our study highlights the potential importance of vertebrate predators in the ecology and evolution of social wasps.