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The potential total number of solitary aculeate wasp and bee species on 34 research sites was estimated using non-parametric Chao and Jackknife tests of presence/absence. Successful estimates of the maximum number of species were achieved for some but not for other sites. Making further visits to a site or removing 'tourist' species data led to further success in estimating the potential number of species. The optimum number of visits required to successfully evaluate the aculeate fauna at a site was determined.

1. Yearly records of worker Vespula germanica (Fabricius) taken in suction traps at Silwood Park (28 years) and at Rothamsted Research (39 years) are examined. 2. Using the autocorrelation function (ACF), a significant negative 1-year lag followed by a lesser non-significant positive 2-year lag was found in all, or parts of, each data set, indicating an underlying population dynamic of a 2-year cycle with a damped waveform. 3. The minimum number of years before the 2-year cycle with damped waveform was shown varied between 17 and 26, or was not found in some data sets. 4. Ecological factors delaying or preventing the occurrence of the 2-year cycle are considered.

Aim: Understanding the role of enemy release in biological invasions requires an assessment of the invader's home range, the number of invasion events and enemy prevalence. The common wasp (Vespula vulgaris) is a widespread invader. We sought to determine the Eurasian origin of this wasp and examined world-wide populations for microsporidian pathogen infections to investigate enemy release. Location: Argentina, Eurasia, New Zealand. Methods: A haplotype network and phylogenetic tree were constructed from combined wasp COI and cytb mitochondrial markers. A morphometric study using canonical discriminant analysis was conducted on wing venation patterns. Microsporidian pathogens prevalence was also examined using small subunit rRNA microsporidia-specific primers. Results: Our spatially structured haplotype network from the native range suggested a longitudinal cline of wasp haplotypes along an east to west gradient. Six haplotypes were detected from New Zealand, and two from Argentina. The populations from the introduced range were genetically similar to the western European, United Kingdom and Ireland. The morphometric analysis showed significant morphological variation between countries and supported the Western European origin for New Zealand populations, although not for Argentine samples. Microsporidian infection rates were highest in New Zealand samples (54%), but no significant differences in infection rates were observed between the invaded and native range. Nosema species included matches to N. apis (a pathogen from honey bees) and N. bombi (from bumble bees). Main conclusions: Multiple introductions of the common wasp have occurred in the invaded range. A high microsporidian infection rate within the native range, combined with multiple introductions and a reservoir of pathogens in other social insects such as bees, likely contributes to the high microsporidian infection rates in the invaded range. Enemy release is likely to be more frequent when pathogens are rare in the home range, or are host specific and rare in reservoir populations of the introduced range. Fil: Lester, P. J.. Victoria University of Wellington; Nueva Zelanda Fil: Gruber, M. A. M.. Victoria University of Wellington; Nueva Zelanda Fil: Brenton Rule, E. C.. Victoria University of Wellington; Nueva Zelanda Fil: Archer, M.. York St. John University; Reino Unido Fil: Corley, Juan Carlos. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Patagonia Norte. Estación Experimental Agropecuaria San Carlos de Bariloche; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Dvorak, L.. Mestske muzeum Marianske Lazne; República Checa Fil: Masciocchi, Maité. Instituto Nacional de Tecnología Agropecuaria. Centro Regional Patagonia Norte. Estación Experimental Agropecuaria San Carlos de Bariloche; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Oystaeyen, A. Van. Katholikie Universiteit Leuven; Bélgica

SYNOPSIS An account is given of worker characteristics, worker activities and brood characteristics in nests of Vespula vulgaris. Variations in queen productivity and efficiency of reproduction are discussed.

When invasive species move to new environments they typically experience population bottlenecks that limit the probability that pathogens and parasites are also moved. The invasive species may thus be released from biotic interactions that can be a major source of densitydependent mortality, referred to as enemy release. We examined for evidence of enemy release in populations of the common wasp (Vespula vulgaris), which attains high densities and represents a major threat to biodiversity in its invaded range. Mass spectrometry proteomic methods were used to compare the microbial communities in wasp populations in the native (Belgium and England) and invaded range (Argentina and New Zealand). We found no evidence of enemy release, as the number of microbial taxa was similar in both the introduced and native range. However, some evidence of distinctiveness in the microbial communities was observed between countries. The pathogens observed were similar to a variety of taxa observed in honey bees. These taxa included Nosema, Paenibacillus, and Yersina spp. Genomic methods confirmed a diversity of Nosema spp., Actinobacteria, and the Deformed wing and Kashmir bee viruses. We also analysed published records of bacteria, viruses, nematodes and fungi from both V. vulgaris and the related invader V. germanica. Thirty-three different microorganism taxa have been associated with wasps including Kashmir bee virus and entomophagous fungi such as Aspergillus flavus. There was no evidence that the presence or absence of these microorganisms was dependent on region of wasp samples (i.e. their native or invaded range). Given the similarity of the wasp pathogen fauna to that from honey bees, the lack of enemy release in wasp populations is probablyrelated to spill-over or spill-back from bees and other social insects. Social insects appear to form a reservoir of generalist parasites and pathogens, which makes the management of wasp and bee disease difficult. Fil: Lester, Philip J. Victoria University of Wellington. Centre for Biodiversity and Restoration Ecology; Nueva Zelanda Fil: Bosch, Peter J. Victoria University of Wellington. Centre for Biodiscovery; Nueva Zelanda. University of Iowa. Department of Biology; Estados Unidos Fil: Gruber, Mónica A. M. Victoria University of Wellington. Centre for Biodiversity and Restoration Ecology; Nueva Zelanda Fil: Kapp, Eugene A. University of Melbourne. Walter and Eliza Hall Institute of Medical Research; Australia Fil: Peng, Lifeng Victoria. University of Wellington. Centre for Biodiscovery; Nueva Zelanda Fil: Brenton-Rule, Evan C. Victoria University of Wellington. Centre for Biodiversity and Restoration Ecology; Nueva Zelanda Fil: Buchanan, Joe. Victoria University of Wellington. Centre for Biodiversity and Restoration Ecology; Nueva Zelanda Fil: Stanislawek, Wlodek L. Ministry for Primary Industries Investigation. Diagnostic Centre—Wallaceville; Nueva Zelanda Fil: Archer, Michael. York St. John University; Inglaterra Fil: Corley, Juan Carlos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Bariloche. Grupo de Ecología de Poblaciones de Insectos; Argentina. Universidad Nacional del Comahue. Centro Regional Universitario Bariloche. Departmento de Ecología; Argentina Fil: Masciocchi, Maite. Instituto Nacional de Tecnología Agropecuaria (INTA). Estación Experimental Agropecuaria Bariloche. Grupo de Ecología de Poblaciones de Insectos; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Van Oystaeyen, Annette. University of Leuven. Laboratory of Socio-Ecology and Social Evolution; Bélgica Fil: Wenseleers, Tom. University of Leuven. Laboratory of Socio-Ecology and Social Evolution; Bélgica

The genus Dolichovespula consists provisionally of 18 species. Aerial nest site characteristics have been established for seven species but most of these species show flexibility in their choice of nest sites and two species often nest in shallow subterranean situations. Colony length is usually just over 3 months to approximately 4 months, but at lower latitudes may extend to more than 5 months. Mature colony size is usually approximately 1000 cells with more large cells than small cells. Parasitized colonies have a shorter colony cycle and smaller colonies. During the production of the sexual brood the larva/worker ratio reaches its lowest value of approximately 2.5 larvae per worker. Colonies often have upper mixed combs of small and large cells. Total adult production is usually less than 2000 adults. Colonies of D. arenaria and D. norwegica may specialize in mainly producing males or queens. Variations in mature colony size and production of queens is probably a consequence of the number of workers present, particularly early in the colony cycle.

Mutual policing is an important mechanism for maintaining social harmony in group-living organisms. In some ants, bees, and wasps, workers police male eggs laid by other workers in order to maintain the reproductive primacy of the queen. Kin selection theory predicts that multiple mating by the queen is one factor that can selectively favor worker policing. This is because when the queen is mated to multiple males, workers are more closely related to queen's sons than to the sons of other workers. Here we provide an additional test of worker policing theory in Vespinae wasps. We show that the yellowjacket Vespula rufa is characterized by low mating frequency, and that a significant percentage of the males are workers' sons. This supports theoretical predictions for paternities below 2, and contrasts with other Vespula species, in which paternities are higher and few or no adult males are worker produced, probably due to worker policing, which has been shown in one species, Vespula vulgaris. Behavioral observations support the hypothesis that V. rufa has much reduced worker policing compared to other Vespula. In addition, a significant proportion of worker-laid eggs were policed by the queen. ispartof: Evolution vol:59 issue:6 pages:1306-14 ispartof: location:United States status: published

Summary 1. Thirteen time series, varying from 17 to 27 years, of the abundance of Vespula germanica and V. vulgaris from lowland England are examined. The time series depend on either spring queens and workers taken in Malaise or suction traps, or collected colonies. 2. During the late 1970s and early 1980s, the abundance of V. germanica declined abruptly but that of V. vulgaris did not. 3. During the early 1980s, the 2-year cycle of annual abundance of V. vulgaris changed to a nearly perfectly damped pattern of annual abundances. 4. The most likely factor causing these population changes was the increased use of pesticides acting directly by killing the wasps and indirectly by reducing their food resources. 5. The difference in response of the two species to increased pesticide use may be related to a difference in foraging ability.

A phylogenetic analysis with the program Hennig86 is performed on the 23 species of the genus Vespa, using the Polistinae and the remaining species of the Vespinae as outgroups. Two species, V. basalis and V. binghami, are unplaced while the remaining 21 species are resolved as a separate group. Within this group the following species groups are resolved as being of uncertain relationships: V. affinis group with 13 species, V. tropica group with five species, V. crabro group with two species and V. orientalis.

We report a case of sudden death due to a catastrophic spontaneous rupture of a urinary bladder associated with megacolon due to a fecal impaction (fecaloma). The massively distended rectum and sigmoid colon filled the pelvic cavity and pressed up against the posterior aspects of the uterus, vagina, and urinary bladder. This produced bladder outlet obstruction, followed by massive dilatation and rupture of the urinary bladder, bilateral hydronephrosis, and a 3.5 liter collection of urinary fluid within the abdominal cavity. Complications of chronic constipation, fecalomas, and rupture of the urinary bladder are reviewed.

1 Six categories of immature and five categories of mature colonies are described and their developmental relationships suggested. 2 Mature brood destroyed by the workers became numerous in 46.4% of the immature colonies. Most of these formed unsuccessful colonies (36.9%) producing few or no queens. The remaining 9.5% recovered to form successful colonies. 3 Successful colonies either reared queens only (mean 356 queens), or queens (mean 1461) and males (mean 254) in their large cells. 4 The number of small cells in mature colonies correlated with the number of cells built by the founder queen. 5 The greater the number of large cells in a mature colony the greater were the chances that a larger proportion of these cells would be used to rear adults. 6 The number of small and large cells are correlated in mature successful colonies. 7 Queen activity and quality are important factors in the control of colony size and success. 8 Selective destruction of male sealed brood in the large cells is linked to worker, rather than queen, control.

Summary 1. Populations of introduced species are often thought to perform differently, or experience different population dynamics, in their introduced range compared to their native habitat. Differences between habitats in climate, competition or natural enemies may result in populations with varying density dependence and population dynamics. 2. We examined the long‐term population dynamics of the invasive common wasp, Vespula vulgaris, in its native range in England and its invaded range in New Zealand. We used 39 years of wasp density data from four sites in England, and 23 years of data from six sites in New Zealand. Wasp population time series was examined using partial rate correlation functions. Gompertz population models and multivariate autoregressive state‐space (MARSS) models were fitted, incorporating climatic variation. 3. Gompertz models successfully explained 59–66% of the variation in wasp abundance between years. Density dependence in wasp populations appeared to act similarly in both the native and invaded range, with wasp abundance in the previous year as the most important variable in predicting intrinsic rate of increase (r). No evidence of cyclic population dynamics was observed. 4. Both the Gompertz and MARSS models highlighted the role of weather conditions in each country as significant predictors of annual wasp abundance. The temporal evolution of wasp populations at all sites was best modelled jointly using a single latent dynamic factor for local trends, with the inclusion of a latent spring weather covariate. That same parsimonious multivariate model structure was optimal in both the native and invaded range. 5. Density dependence is overwhelmingly important in predicting wasp densities and ‘wasp years’ in both the native and invaded range. Spring weather conditions in both countries have a major influence, probably through their impact on wasp colony initiation and early development. The population dynamics in the native range and invaded range show no evidence of cyclic boom‐and‐bust dynamics. Invasive species may not exhibit different population dynamics despite considerable variation in abundances throughout their distribution.