The wing coupling apparatus and the morphometric analysis of honeybee populations

Significant differences between countries were found in the distribution of the number of hamuli within Apis andreniformis, A. florea, A. cerana and A. koschevnikovi. The mean hamuli numbers for Apis mellifera intermissa differed significantly among localities in Algeria. Significant differences in intercolonial variability between countries were found within A. cerana. There was no significant infraspecific variability within A. andreniformis, A. florea, A. koschevnikovi and A. m. intermissa. Significant differences in the mean number of hamuli occur between A. m. intermissa and A. andreniformis, A. florea and A. cerana; also between A. cerana/A. koschevnikovi and A. andreniformis and A. florea. Significant differences were found in the distribution and variability of the number of hamuli between species (populations). The mean numbers of hamuli for A. andreniformis differed from those of A. florea. Both these population means differed from those of A. cerana, A. koschevnikovi and A. m. intermissa. No significant differences were found between A. cerana and A. koschevnikovi. When the analysis included data for A. dorsata, A. nigrocincta, A. m. carnica, A. m. caucasica and A. m. ligustica, the results showed significant differences in hamuli numbers between A. andreniformis/A. florea and A. cerana/A. koschevnikovi/A. nigrocincta and A. m. intermissa/A. m. carnica/A. m. caucasica/A. m. ligustica. Hamuli numbers in A. dorsata significantly differed from those of other populations except A. m. intermissa. These results show that hamuli numbers are useful in the classification of honeybee populations. Whether hamuli would be useful in multivariate analysis depends on the correlation between the number of hamuli and the other characters used

Parasitic Cape bees in the northern regions of South Africa: source of the founder population

Multivariate discriminant analyses of nine standard morphometric characters of honeybee workers were used to track the origin of a social parasitic pseudo-clone of thelytokous laying workers that have invaded colonies of Apis mellifera scutellata in South Africa. Twenty social parasitic workers were sampled from both of two infested A. m. scutellata colonies at two distant apiaries (Graskop and Heilbronn, about 390 km apart) and compared with data obtained from 80 colonies in four different geographical zones (zone I: thelytokous A. m. capensis morphocluster; zone II: natural thelytokous hybrids between A. m. capensis and A. m. scutellata; zone III: thelytokous A. m. scutellata morphocluster; zone IV: an arrhenotokous A. m. scutellata morphocluster). Thelytokous laying workers occur naturally in zones I-III. Highly significant morphometric differences were found among the bees in the four zones. The data support the conclusion that the social parasitic workers belong to the thelytokous A. m. capensis morphocluster. It is most likely that the social parasitic workers originated from the heart of the Cape bee's distribution range in the Western Cape region in zone I. Morphometric analysis makes it feasible to restrict the possible origin of the social parasitic workers from the natural distribution range of thelytoky (approximately 240 000 km2) down to about 12 000 km2, which represents a resolution capacity of about 95%

Apis florea in Jordan: source of the founder population

A recent isolated population of Apis florea has been reported from Aqaba in Jordan at the Red Sea, consisting of numerous colonies within a still limited range which apparently is expanding. This region is about 1500 km apart from its next occurrences in Sudan where it had been introduced and first detected in 1985 and about 2000 km apart from its next natural occurrences in Iran and Oman. These bees apparently have been imported by human transport, most likely by ship. This new location thus represents a major jump in the progression of the species still to fill a wide area of possible locations offering adequate living conditions. Here we attempt to track the possible origin of this new population by morphometric methods. This analysis indicated closest relation to A. florea from Oman, thus being the most likely source of this population

A scientific note on the natural merger of two honeybee colonies (Apis mellifera capensis)

Natural mergers of honeybee colonies are commonplace in tropical Africa (Hepburn and Radloff, 1998), but their consequences on organizational structure are unknown. Here we determine the spatial distribution and division of labor of workers (Apis mellifera capensis Esch.) following a merger of two colonies. Two unrelated colonies (each ~3000 bees) were placed in threeframe observation hives. When workers emerged from the sealed brood of each colony, they were individually labeled and reintroduced into their respective mother hives. They are referred to as cohorts Aand B, each comprising 300 workers of the same age. The behaviors and positions of all labeled workers and queens were recorded twice daily for 24 days (Kolmes, 1989; Pirk et al., 2000). On day 14 colony B was dequeened, left its nest and merged with colony A on day 15

The buckling response of symmetrically laminated composite plates having a trapezoidal planform area

The focus of this work is the buckling response of symmetrically laminated composite plates having a planform area in the shape of an isosceles trapezoid. The loading is assumed to be inplane and applied perpendicular to the parallel ends of the plate. The tapered edges of the plate are assumed to have simply supported boundary conditions, while the parallel ends are assumed to have either simply supported or clamped boundary conditions. A semi-analytic closed-form solution based on energy principles and the Trefftz stability criterion is derived and solutions are obtained using the Rayleigh-Ritz method. Intrinsic in this solution is a simplified prebuckling analysis which approximates the inplane force resultant distributions by the forms Nx=P/W(x) and Ny=Nxy=0, where P is the applied load and W(x) is the plate width which, for the trapezoidal planform, varies linearly with the lengthwise coordinate x. The out-of-plane displacement is approximated by a double trigonometric series. This analysis is posed in terms of four nondimensional parameters representing orthotropic and anisotropic material properties, and two nondimensional parameters representing geometric properties. For comparison purposes, a number of specific plate geometry, ply orientation, and stacking sequence combinations are investigated using the general purpose finite element code ABAQUS. Comparison of buckling coefficients calculated using the semi-analytical model and the finite element model show agreement within 5 percent, in general, and within 15 percent for the worst cases. In order to verify both the finite element and semi-analytical analyses, buckling loads are measured for graphite/epoxy plates having a wide range of plate geometries and stacking sequences. Test fixtures, instrumentation system, and experimental technique are described. Experimental results for the buckling load, the buckled mode shape, and the prebuckling plate stiffness are presented and show good agreement with the analytical results regarding the buckling load and the prebuckling plate stiffness. However, the experimental results show that for some cases the analysis underpredicts the number of halfwaves in the buckled mode shape. In the context of the definitions of taper ratio and aspect ratio used in this study, it is concluded that the buckling load always increases as taper ratio increases for a given aspect ratio for plates having simply supported boundary conditions on the parallel ends. There are combinations of plate geometry and ply stackling sequences, however, that reverse this trend for plates having clamped boundary conditions on the parallel ends such that an increase in the taper ratio causes a decrease in the buckling load. The clamped boundary conditions on the parallel ends of the plate are shown to increase the buckling load compared to simply supported boundary conditions. Also, anisotropy (the D16 and D26 terms) is shown to decrease the buckling load and skew the buckled mode shape for both the simply supported and clamped boundary conditions

Social parasitism by honeybee workers (Apis mellifera capensis Escholtz): host finding and resistance of hybrid host colonies

We studied possible host finding and resistance mechanisms of host colonies in the context of social parasitism by Cape honeybee (Apis mellifera capensis) workers. Workers often join neighboring colonies by drifting, but long-range drifting (dispersal) to colonies far away from the maternal nests also rarely occurs. We tested the impact of queenstate and taxon of mother and host colonies on drifting and dispersing of workers and on the hosting of these workers in A. m. capensis, A. m. scutellata, and their natural hybrids. Workers were paint-marked according to colony and reintroduced into their queenright or queenless mother colonies. After 10 days, 579 out of 12,034 labeled workers were recaptured in foreign colonies. We found that drifting and dispersing represent different behaviors, which were differently affected by taxon and queenstate of both mother and host colonies. Hybrid workers drifted more often than A. m. capensis and A. m. scutellata. However, A. m. capensis workers dispersed more often than A. m. scutellata and the hybrids combined, and A. m. scutellata workers also dispersed more frequently than the hybrids. Dispersers from queenright A. m. capensis colonies were more often found in queenless host colonies and vice versa, indicating active host searching and/or a queenstate-discriminating guarding mechanism. Our data show that A. m. capensis workers disperse significantly more often than other races of A. mellifera, suggesting that dispersing represents a host finding mechanism. The lack of dispersal in hybrids and different hosting mechanisms of foreign workers by hybrid colonies may also be responsible for the stability of the natural hybrid zone between A. m. capensis and A. m. scutellata

Bee-hawking by the wasp, Vespa velutina, on the honeybees Apis cerana and A. mellifera

The vespine wasps, Vespa velutina, specialise in hawking honeybee foragers returning to their nests. We studied their behaviour in China using native Apis cerana and introduced A. mellifera colonies. When the wasps are hawking, A. cerana recruits threefold more guard bees to stave off predation than A. mellifera. The former also utilises wing shimmering as a visual pattern disruption mechanism, which is not shown by A. mellifera. A. cerana foragers halve the time of normal flight needed to dart into the nest entrance, while A. mellifera actually slows down in sashaying flight manoeuvres. V. velutina preferentially hawks A. mellifera foragers when both A. mellifera and A. cerana occur in the same apiary. The pace of wasp-hawking was highest in mid-summer but the frequency of hawking wasps was three times higher at A. mellifera colonies than at the A. cerana colonies. The wasps were taking A. mellifera foragers at a frequency eightfold greater than A. cerana foragers. The final hawking success rates of the wasps were about three times higher for A. mellifera foragers than for A. cerana. The relative success of native A. cerana over European A. mellifera in thwarting predation by the wasp V. velutina is interpreted as the result of co-evolution between the Asian wasp and honeybee, respectively

Reproductive Biology of the Cape Honeybee: A Critique of Beekman et al: A critique of "Asexually Produced Cape Honeybee Queens (Apis mellifera capensis) Reproduce Sexually,” authors: Madeleine Beekman, Michael H. Allsopp, Julianne Lim, Frances Goudie, and Benjamin P. Oldroyd. Journal of Heredity. 2011:102(5):562-566

Laying workers of the Cape honeybee parthenogenetically produce female offspring, whereas queens typically produce males. Beekman et al. confirm this observation, which has repeatedly been reported over the last 100 years including the notion that natural selection should favor asexual reproduction in Apis mellifera capensis. They attempt to support their arguments with an exceptionally surprising finding that A. m. capensis queens can parthenogenetically produce diploid homozygous queen offspring (homozygous diploid individuals develop into diploid males in the honeybee). Beekman et al. suggest that these homozygous queens are not viable because they did not find any homozygous individuals beyond the third larval instar. Even if this were true, such a lethal trait should be quickly eliminated by natural selection. The identification of sex (both with molecular and morphological markers) is possible but notoriously difficult in honeybees at the early larval stages. Ploidy is however a reliable indicator, and we therefore suggest that these "homozygous” larvae found in queen cells are actually drones reared from unfertilized eggs, a phenomenon well known by honeybee queen breeder

Plasmonic atoms and plasmonic molecules

The proposed paradigm of plasmonic atoms and plasmonic molecules allows one to describe and predict the strongly localized plasmonic oscillations in the clusters of nanoparticles and some other nanostructures in uniform way. Strongly localized plasmonic molecules near the contacting surfaces might become the fundamental elements (by analogy with Lego bricks) for a construction of fully integrated opto-electronic nanodevices of any complexity and scale of integration.Comment: 30 pages, 16 figure

Multivariate morphometric analysis of Apis cerana of southern mainland Asia

Multivariate morphometric analyses were performed on a series of worker honeybees, Apis cerana, representing 557 colonies from all of southern mainland Asia extending from Afghanistan to Vietnam south of the Himalayas. Scores from the principal components analysis revealed five statistically separable but not entirely distinct morphoclusters of bees: (1) the Hindu Kush, Kashmir, N. Myanmar, N. Vietnam and S. China; (2) Himachal Pradesh region of N. India; (3) N. India, Nepal; (4) central and S. Myanmar and Vietnam, Cambodia, Thailand, S. China and peninsular Malaysia; (5) central and S. India. The major morphoclusters are distributed coherently with the different climatic zones of the region. While populations are definable, nomenclatural adjustments remain for the future