Interactions between the Social Digger Wasp, <Emphasis Type="Italic">Cerceris rubida</Emphasis>, and Its Brood Parasitic Flies at a Mediterranean Nest Aggregation

The fitness consequence of many behaviours of the small digger wasp, Cerceris rubida (Hymenoptera: Crabronidae), the only European species of its genus in which females share nests, are still unknown. Here, I present novel data on the nesting patterns and nest parasites of an Italian population of this wasp, with emphasis on which behavioural strategies may have evolved to reduce brood parasitism. Nests were established mainly in horizontal surfaces with scarce vegetation and hard soil, resulting in spatially clumped nests; the extent of nest aggregation increased over a 6-year period. Wasp brood cells are attacked by the miltogrammine fly Pterella grisea (Diptera: Sarcophagidae), which waits for nest-returning wasps on perching sites and then follows them in flight (satellite flight), eventually landing on the nest entrance and larvipositing without entering further in the tunnel. This technique seems to be adaptive for the parasitic flies, which would be rejected from nests by the guarding wasps if attempting to enter. The daily activity of the flies closely matched the host wasp’s provisioning activity, but C. rubida females were able to partially confound the tracking flies by performing evasive manoeuvres while returning to the nest. Patches with higher nest density and nests with more resident females did suffer more fly landings on nest entrances (a prerequisite for larviposition). These trends, however, disappeared on a per nest basis and on a per wasp provisioning flight basis, respectively. Across two years, only 6% of brood cells were parasitized, a picture similar to what observed for miltogrammine flies at nest aggregations of other Cerceris spp., and new data are necessary to test if there is a benefit of either nest density or nest sharing against P. grisea parasitism.     

Few, small, and male: multiple effects of reduced nest space on the offspring of the solitary wasp, Euodynerus (Pareuodynerus) posticus (Hymenoptera: Vespidae)

The size of the preexisting wood cavities used as nests by aculeate Hymenoptera is expected to have consequences on fitness parameters such as offspring number and size. We evaluated the consequences of using small and large (three-times more voluminous) trap-nests by the solitary wasp, Euodynerus (Pareuodynerus) posticus (Herrich-Schaeffer). Following life-history and sex allocation theories, a number of non-mutually exclusive hypotheses were formulated: i.e. small nests either produce smaller or fewer offspring and/or more males, the cheaper sex. Wasps built about 28% more, but shorter brood cells in large nests, although their volume was still much higher in large nests. Adult males had smaller body size in small nests, but female size did not differ between large and small nests, possibly as an adaptive response against the future higher foraging costs of size-reduced females. Sex-ratio was often biased towards males in small nests. Mortality did not differ between large and small nests. We conclude that E.?(P.) posticus females would benefit from using larger nests, but that the sex-ratio would be probably overall unbalanced if females would not use also smaller, male-oriented tunnels.     

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.     

Nesting activity of cavity-nesting bees and wasps is lower in small-scale apple orchards compared to nearby semi-natural habitats

1. Commercially reared cavity-nesting bees have been studied mainly in large, intensively managed orchards. However, knowledge on wild cavity-nesting bee and wasp communities and their potential limitations in smaller orchards remain insufficient.
2. We compared the colonization rate of trapnests, nesting success, parasitism and response to flower resources of cavity-nesting bees and wasps between apple orchards and nearby semi-natural habitats (SNHs).
3. Trapnests were placed in orchards and neighbouring SNHs. Colonization dynamics were studied and herbaceous flower resources were estimated. Furthermore, nest and brood cell quantity, number of alive offspring and nest parasitism rate were assessed.
4. We found a higher colonization rate in the SNHs than in the orchards. Both bees and wasps made more nests, completed more brood cells and had a higher number of alive offspring in the SNHs. The number of bee nests in the orchards showed a positive correlation with the species richness of the flowering plants. The nest parasitism of wasps was higher in the SNHs.
5. Apple orchards in the studied small-scale system were generally less colonized by cavity-nesting hymenopterans than nearby SNHs that can be important reservoirs of these ecosystem service provider hymenopterans. Our results highlight the importance of diverse flowering herbaceous vegetation in the understory that increased the number of bee nests in orchards and that could have a positive effect on the nesting activity of the bee species active in summer. Therefore, management practices that support flowering plant species in the understory vegetation are highly recommended in such orchards.

     

Parasites favour intermediate nestling mass and brood size in cliff swallows

A challenge of life‐history theory is to explain why animal body size does not continue to increase, given various advantages of larger size. In birds, body size of nestlings and the number of nestlings produced (brood size) have occasionally been shown to be constrained by higher predation on larger nestlings and those from larger broods. Parasites also are known to have strong effects on life‐history traits in birds, but whether parasitism can be a driver for stabilizing selection on nestling body size or brood size is unknown. We studied patterns of first‐year survival in cliff swallows (Petrochelidon pyrrhonota) in western Nebraska in relation to brood size and nestling body mass in nests under natural conditions and in those in which hematophagous ectoparasites had been removed by fumigation. Birds from parasitized nests showed highest first‐year survival at the most common, intermediate brood‐size and nestling‐mass categories, but cliff swallows from nonparasitized nests had highest survival at the heaviest nestling masses and no relationship with brood size. A survival analysis suggested stabilizing selection on brood size and nestling mass in the presence (but not in the absence) of parasites. Parasites apparently favour intermediate offspring size and number in cliff swallows and produce the observed distributions of these traits, although the mechanisms are unclear. Our results emphasize the importance of parasites in life‐history evolution.     

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.     

Comparative analysis of thermoregulation in the nests of certain species of social insects

Studies have been made on thermal regulation in the nests of families of the honey bee Apis mellifera, wasp Dolihovespula silvestris and bumblebees Bombus terrestris, B. agrorum and B. lapidaris during their maximum development. It was shown that thermoregulation significantly stimulated the brood in the nest. Among the species investigated, the highest thermoregulatory capacities are exhibited by honey bees, this fact being associated with the large number of individuals in their colonies. During cooling, bees group around the brood and their bodies make a cover of thermal insulation. Sheltering of the nests plays the main role in heat preservation of wasps and bumblebees. The latter, using contact method of heating of cells with the brood, provide rather constant temperature for its development. Honey bees, wasps and bumblebees react to overheating in the nests essentially in a similar way, i. e. by active aeration of their nests by vigorous wing beatings. The frequency of beatings increases with the increase in temperature.     

Opportunistic predation and offspring sex ratios of cicada-killer wasps (Sphecius speciosus Drury)

Abstract.  1. The way in which hunting of prey affects the sex ratio of the predator's offspring is not well understood. Female cicada-killer wasps are convenient for study because they specialise in capturing cicadas to provision their offspring. Cicada prey are nearly twice as heavy as the wasps that carry them, hence some degree of prey selectivity by the wasps is to be expected. It has been suggested that wasps bias their offspring towards females by foraging selectively for female prey, whereas there is some evidence that sex ratios are actually male-biased. This study was designed to establish the connection between foraging and offspring sex ratio.
2. Three, non-exclusive, hypotheses of selective predation were tested. The frequency of predation on different classes of prey in conjunction with their availability was estimated by intercepting the wasps on their way to their nests and by sampling cicadas in the environment. The hypothesis of selective predation was not supported; predation appears to be opportunistic and non-selective. Cicada prey weight was not a simple linear function of wasp weight, although the smallest wasps were constrained to carry small prey.
3. Wasp offspring (larvae) were excavated from subterranean nests and found to be male-biased (3 : 1 or 4 : 1) in 2 years. The observed ratios are close to expectation from Fisher's equal-investment model, taking account of sexual size dimorphism, and are evidently unrelated to the sex of the prey. A simple binomial probability rule of sex allocation provides a behavioural mechanism for producing the observed sex ratio of offspring.     

SEX-RATIO MANIPULATION IN RESPONSE TO HOST SIZE BY THE PARASITOID WASP SPALANGIA CAMERONI: A LABORATORY STUDY

The prediction of Charnov et al.'s (1981) host-size model that there should be a negative relationship between host size and wasp sex ratio (proportion sons) was supported for Spalangia cameroni, a solitary parasitoid wasp. The relationship was shown to be a result of offspring sex manipulation by females in response to host size rather than a result of differential mortality of the sexes. A major assumption of the host-size model is that host size has a greater effect on the ultimate reproductive success of emerging female wasps than of males. This assumption was not supported. Host size had a positive effect on the size of both male and female S. cameroni. However, neither host size nor wasp size affected longevity, production of offspring by females, or ability of males to compete for mates. Host size may differentially affect the reproductive success of female and male wasps through effects on other aspects of reproductive success. Tests of the assumptions of offspring sex-ratio manipulation hypotheses are scarce but critical, not only for parasitoid wasps, but also for other organisms.     

Molecular markers reveal reproductive strategies of non‐pollinating fig wasps

1. Fig wasps have proved extremely useful study organisms for testing how reproductive decisions evolve in response to population structure. In particular, they provide textbook examples of how natural selection can favour female‐biased offspring sex ratios, lethal combat for mates and dimorphic mating strategies. 2. However, previous work has been challenged, because supposedly single species have been discovered to be a number of cryptic species. Consequently, new studies are required to determine population structure and reproductive decisions of individuals unambiguously assigned to species. 3. Microsatellites were used to determine species identity and reproductive patterns in three non‐pollinating Sycoscapter species associated with the same fig species. Foundress number was typically one to five and most figs contained more than one Sycoscapter species. Foundresses produced very small clutches of about one to four offspring, but one foundress may lay eggs in several figs. 4. Overall, the data were a poor match to theoretical predictions of solitary male clutches and gregarious clutches with n ? 1 females. However, sex ratios were male‐biased in solitary clutches and female‐biased in gregarious ones. 5. At the brood level (all wasps in a fig), a decrease in sex ratio with increasing brood size was only significant in one species, and sex ratio was unrelated to foundress number. In addition, figs with more foundresses contain more wasp offspring. 6. Finally, 10–22% of females developed in patches without males. As males are wingless, these females disperse unmated and are constrained to produce only sons from unfertilised eggs.     

Scaling in nests of a social wasp: a property of the social group

The numbers of brood cells in nests built by founding swarms of the Neotropical social wasp Polybia occidentalis closely correlate with the numbers of wasps in the swarms. We analyzed nests of different sizes to determine how they scale with respect to the allocation of brood cells among combs. Three patterns were evident: compared to smaller nests, larger nests have (1) more combs and (2) larger combs; and (3) among nests containing the same number of combs, the last two combs diverge in relative size as nest size increases. Taken together, these results suggest that members of a swarm somehow "know" the size of the swarm they are in. This information feeds back to individual builders, which quantitatively modulate their responses to stigmergic cues in ways that result in the nest-size-scaled allocation of brood cells among combs. The patterns also suggest that swarms fine-tune the final size of their nests by making corrections as they build.     

Nesting biology of four species of Trypoxylon (Trypargilum) (Hymenoptera: Crabronidae) in Chaco Serrano woodland, Central Argentina

Trypoxylon (Trypargilum) (Crabronidae) wasps are solitary spider predators that can build their nests in artificial trap-nests, which enables study of their nesting architecture and biology. Twenty traps (each containing 15-30 internodes of cane) were placed in each of nine sites of Chaco Serrano Woodland in Central Argentina (Córdoba) in October 2005, and were recovered in June 2006. We obtained 91 nests of four species of Trypoxylon (Trypargilum). In the laboratory, each Trypoxylon nest was sectioned longitudinally to study its architecture. The number of brood cells was counted, and the occurrence and length of vestibular and intercalary cells and the pre-closing plug space were recorded. We measured the diameter of the cane entrance, total length of the nest, length of each brood cell, maximum thickness of mud partitions and closing plug thickness. We also recorded the cell contents: the wasps, their natural enemies and the prey spiders. Mortality was assessed and the sex ratio calculated for each species. Finally, the nests were examined to help clarify the function of the vestibular cell. The nest architecture was similar in the four species, with linear brood cells located one after the other separated by mud partitions, as in other species of the subgenus Trypargilum. Forty-eight percent of the nests had vestibular cells, but only two had intercalary cells. The thickness of the mud partitions and the length of the brood cells differed among species and were related to the size of the emerged wasp. The diameter of the nest entrance was directly related to the average length of the fore-tibia. Sex ratios of all species did not deviate from 0.5. Mortality due to parasitoids (Eulophidae; Melittobia sp.) was similar among species, while the mortality due to cuckoo wasps (Chrysididae) in T. lactitarse was higher than in the other species. The presence of vestibular cells was not related either to the mortality due to natural enemies or to the orientation of the trap in the field. Spiders in the family Araneidae were the most frequently collected prey.     

Why make daughters larger? Maternal sex-allocation and sex-dependent selection for body size in a mass-provisioning wasp, Trypoxylon politum

Mass-provisioning wasps package maternal investment into broodcells, sealed structures that contain all the provisions necessaryfor an offspring's growth and development. Optimal sex-allocationtheory predicts that if maternal provisions determine the sizeof each offspring, and the amount of provisions available toeach offspring varies, females should allocate well-stockedbrood cells to the sex that benefits most from being large.I tested this hypothesis using observations of organ-pipe wasps,Trypoxylon politum, and dissections of their nests. A Mississippipopulation of T. politum was intensively studied from 1993 to1995. This population fit the assumptions of optimal sex-allocationmodels by Green and Brockmann and Grafen. Female weight at emergencewas 1.29 times that of males, and wing length was 1.15 timesthat of males. This discrepancy in size occurred because thevolume of parental provisions strongly influenced adult bodysize, and better-stocked brood cells were preferentially allocatedto daughters. Brood-cell volume correlated with both wing lengthand weight at emergence in both sexes, and the chance that agiven brood cell contained a female offspring increased withincreasing brood-cell volume. Fitness was positively relatedto body size for females, but I found no evidence of an advantageto large males. Although there was evidence of stabilizing selectionfor male wing length in one year, there was no evidence of anincreasing relationship between body size and fitness (directionalselection) for males in either 1993 or 1994. Female fecunditywas positively related to body size in both years, indicatingthat larger females have increased reproductive success. Therate at which females provisioned brood cells was also correlatedwith body size. Observed patterns of investment in brood cellsare quantitatively consistent with the predictions of optimalsex-allocation theory, but certain aspects of female provisioningbehavior suggest females are not following a single "optimal"strategy. Patterns of provisioning were variable among differentfemales at the study site during the same year. Large femalestended to produce larger offspring. Although Brockmann and Grafen'smodel predicts a single, population wide "switchpoint" fromthe production of male to female offspring, there was no evidencefor such a switchpoint     

How selfish is a cowbird nestling?

Brood-parasitic young are reared in the nests of different species and can derive no genetic benefit from the survival of host offspring. However, although the nestlings of many parasitic cuckoo and honeyguide species routinely kill host young soon after hatching, nestling brown-headed cowbirds, Molothrus ater, tolerate host offspring and are commonly reared alongside them for at least part of the nestling period. I used comparative analyses of data from the literature to investigate whether brown-headed cowbird nestlings gain direct benefits by allowing host young to live. The brown-headed cowbird (44 g) parasitizes many passerines (adult mass range about 5-90 g) and the likelihood that host young survive to fledge from parasitized nests varies between species. In common with previous work, I found that host offspring mortality was highest in species whose offspring were relatively small compared with the cowbird nestling. Furthermore, cowbird nestlings were most likely to fledge when reared alongside host young of intermediate size. In these nests, one or two host young typically fledged as well. I suggest that cowbirds, and other host-tolerant brood parasites, could benefit from the presence of host nestlings through the assistance that host chicks offer in soliciting a higher provisioning rate, and that such benefits might outweigh the costs of having competition for food at each nest visit. Variation in this cost-benefit ratio could explain differences between brood parasite species in their tolerance of host young.     

Les relations entre fourmis arboricoles et guêpes sociales sous les tropiques

Due to the brood that it contains, the nest of social wasps constitutes a major source of protein for eventual predators. In the tropics, ants are generally considered as the most efficacious among them. In the face of such predation, wasps have developed over the course of evolution a great number of strategies. In addition to guarding and defensive behaviours displayed by workers, social wasps have nests whose structure is a response to the predation pressure exerted by ants. Thus, the presence of a petiole attaching the nest to a natural support itself sometimes selected because of its limited accessibility constitutes a frequent example of architectural defence. The effectiveness of the petiole is often improved through the repeated application of repellent substances on its surface. In the same way, wasps that found their new societies through swarming construct nests protected by an envelope. In the American tropics, army ants which hunt on the ground and can rapidly take over a tree, regularly pillage wasp nests. Because no defensive strategy is efficacious against such predators, the choice of nest site becomes decisive. Paradoxically, it is by nesting in close proximity to an arboreal ant nest that certain wasp species have been able to find a way of responding to the threat exerted by other ants. These ants, which tolerate the presence of the wasp nest, are capable of efficaciously protecting the tree or the branch sheltering the nest.     

High hemocyte load is associated with increased resistance against parasitoids in Drosophila suzukii, a relative of D. melanogaster

Among the most common parasites of Drosophila in nature are parasitoid wasps, which lay their eggs in fly larvae and pupae. D. melanogaster larvae can mount a cellular immune response against wasp eggs, but female wasps inject venom along with their eggs to block this immune response. Genetic variation in flies for immune resistance against wasps and genetic variation in wasps for virulence against flies largely determines the outcome of any fly-wasp interaction. Interestingly, up to 90% of the variation in fly resistance against wasp parasitism has been linked to a very simple mechanism: flies with increased constitutive blood cell (hemocyte) production are more resistant. However, this relationship has not been tested for Drosophila hosts outside of the melanogaster subgroup, nor has it been tested across a diversity of parasitoid wasp species and strains. We compared hemocyte levels in two fly species from different subgroups, D. melanogaster and D. suzukii, and found that D. suzukii constitutively produces up to five times more hemocytes than D. melanogaster. Using a panel of 24 parasitoid wasp strains representing fifteen species, four families, and multiple virulence strategies, we found that D. suzukii was significantly more resistant to wasp parasitism than D. melanogaster. Thus, our data suggest that the relationship between hemocyte production and wasp resistance is general. However, at least one sympatric wasp species was a highly successful infector of D. suzukii, suggesting specialists can overcome the general resistance afforded to hosts by excessive hemocyte production. Given that D. suzukii is an emerging agricultural pest, identification of the few parasitoid wasps that successfully infect D. suzukii may have value for biocontrol.     

How can cleptoparasitic drosophilid flies emerge from the closed brood cells of the red Mason bee?

Aculeate Hymenoptera provision their progeny with large amounts of food. To protect their investment against brood parasites, females of many bee and wasp species construct brood cells that are hard to penetrate when finally sealed. However, the sealed brood cells also pose a problem for parasites that oviposit in the brood cell during provisioning. Brood parasites are smaller than their host and may lack strong mandibles to break through the solid brood cell walls. Furthermore, in nests built in existing cavities, newly‐eclosed brood parasites need information about the location of the nest entrance. In the present study, the mechanisms of emergence are investigated in Cacoxenus indagator Loew (Diptera, Drosophilidae), the major cleptoparasite in nests of the red Mason bee Osmia bicornis L. (Hymenoptera, Megachilidae). Larvae of C. indagator move to brood cells closer to the nest entrance and sometimes make small emergence holes in the final closure of the nest entrance. Nevertheless, approximately one‐third of newly‐eclosed flies orientate and break through at least one intact cell partition to emerge. Flies make most of their attempts to emerge at the correct side (i.e. the one pointing to the nest entrance, probably by using the shape of the cell partition as a cue). Newly‐eclosed flies use their head blister (ptilinum) to exert hydraulic pressure on particles of the cell partitions and produce small holes. Thus, C. indagator exhibits a set of behavioural and physiological adaptations enabling them to successfully emerge even from closed brood cells of their host.     

Determination of the optimal parasitoid‐to‐host ratio for efficient mass‐rearing of the parasitoid,Sclerodermus pupariae (Hymenoptera: Bethylidae)

Sclerodermus pupariae Yang et Yao (Hymenoptera: Bethylidae) is used as a potential biocontrol agent for several buprestid and cerambycid larvae. This study aimed to enhance the efficiency of mass‐rearing of this parasitoid by investigating the fitness gain of this bethylid wasp, including the proportion of successful parasitism and development, brood size, sex ratio, proportion of winged female offspring, body size and longevity of female offspring, under eight different maternal parasitoid density treatments using Thyestilla gebleri Faldermann as host in the laboratory. The results indicated that the foundress densities did not affect the parasitism or emergence rate of this parasitoid. Brood size of the parasitoids increased significantly when the number of maternal wasps ranged from one to four. However, further increases in foundress number did not affect the parasitoid brood size. The sex ratios of S. pupariae were always female‐biased. The proportions of male in the progeny colonies were <10% throughout all experimental treatments. The percentage of winged female progeny was not significantly influenced by the density of adult maternal parasitoids. Body sizes of parasitoids significantly declined with increasing maternal parasitoid densities. Although the parasitoid body size reduced when maternal wasp number was higher, it could be compromised by the relatively higher number of female offspring produced. Further, more than 70% of the parasitoids remained alive when they were stored at 12°C for four months throughout the experiments. These findings suggest that exposure of four female wasps to a single host larva would result in the highest fitness of S. pupariae. Our findings might provide a new approach to enhance the efficiency of mass‐rearing of this bethylid wasp.     

Ectoparasites and reproductive trade-offs in the barn swallow (Hirundo rustica)

Parents are predicted to trade offspring number and quality against the costs of reproduction. In altricial birds, parasites can mediate these costs because intensity of parasitism may increase with parental effort. In addition, parasites may mediate a trade-off between offspring number and quality because nestlings in large broods may have reduced anti-parasite immune defence. In this study, we experimentally analysed the effect of brood size on infestation by an ectoparasitic mite in nests of barn swallows (Hirundo rustica). Nests with an enlarged brood had larger prevalence and intensity of infestation than those with a reduced brood. Importantly, each nestling in enlarged broods was exposed to a larger number of mites, even when measured on a per nestling basis, than in reduced broods. Nestlings in enlarged broods had smaller body mass and T-cell-mediated immune response compared to reduced broods. T-cell-mediated immune response and feather growth were negatively correlated with per nestling intensity of infestation in enlarged but not in reduced broods. The results suggest that nestlings in enlarged broods have depressed immunity leading to larger per nestling mite infestation. Hence, exposure to parasites of offspring and parents increases with brood size, and parasitism can thus mediate trade-offs between reproduction and number and quality of the progeny in the barn swallow.     

Habitat structure components are effective predictors of trap-nesting Hymenoptera diversity

Habitat heterogeneity can be the major factor affecting species diversity in a community and measuring bee and wasp community habitat preferences in natural systems may provide insights for biodiversity management and conservation. In the present study, we investigate the effects of habitat structure components on solitary bee and wasp species richness and abundance. The research was conducted in an urban forest remnant in southeast Brazil. Our main questions were: (1) is similarity in habitat structure mirrored by similarity in Aculeate assemblage composition? and (2) what are the vegetation features that could be used as predictors of solitary bee and wasp richness and abundance? Aculeate bees and wasps were sampled using trap nests from February to November 2004. Trap nests were placed in sampling units located in 6 ha of secondary mesophytic forest. One hundred and thirty-seven trap nests were occupied by four species of wasps and seven species of bees. Altogether, our sampling units had a mean capture rate (relative to expected richness) of 72% during all the study period. The more similar sampling units were in terms of vegetation structure, the more similar they were in solitary bee and wasp species composition. The variance of tree abundance, shrub height and the abundance of wood logs were good predictors of solitary bee and wasp species richness and abundance in the study area. We demonstrate that even in a small scale it is possible to detect significant influences of habitat features on alpha diversity and that some of them are effective as predictors of trap-nesting Hymenoptera richness and abundance.