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

Temporal scales of variation in settlement and recruitment of the mussel Perna perna (Linnaeus, 1758)

Population dynamics of many intertidal organisms are strongly affected by the abundance and distribution of larvae arriving on the shore. In particular, not only absolute numbers of settlers but also the degree of synchronisation of settlement can have a strong influence on whether density-dependent or density-independent processes shape adult shape populations. Temporal variation in rates of settlement and recruitment of the mussel Perna perna on the south coast of South Africa was investigated using a nested spatial design at different temporal scales. Variability in settlement at spring tides was examined at two temporal scales: lunar (to investigate the effect of state of the moon on settlement) and tidal (to investigate the influence of state of the tide on mussel settlement). Recruitment over neap tides was examined at one temporal scale, fortnight (to investigate the effect of date on mussel recruitment). Strong temporal variation was evident for both settlement and recruitment, but not at all time scales. Distinct peaks of settler/recruit abundance were observed during the lunar and neap tide studies. Recruitment intensity differed over the course of the year, and pulsing of recruitment was generally synchronised among locations. However, the strength of pulsing differed dramatically among locations, giving a significant interaction between fortnight and location. The finest temporal scale, investigated in the tidal study, did not reveal a significant effect of the state of the tide on settlement. The state of the moon (new or full) was not significant as a main factor (p = 0.052), although generally more settlers arrived on the shore during new moon. Phase of the moon appeared to have an effect on settler abundances, but only when and where densities were high

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

Multivariate analysis of selected honeybee populations in Africa

Morphometric characters and sting pheromones of worker honeybees, Apis mellifera Linnaeus were analysed by multivariate methods to characterise selected honeybee populations along five transects in Africa at a meso-scale level of sampling distance resolution. In some, but not all, areas pheromonal clusters were found to be coincident and concordant with the morphometric clusters, thus indicating that different honeybee traits have dispersed variably among populations. All transects were found to contain areas of significantly high variance. High intracolonial variance was taken to indicate localised genetic variation coupled with out-cross matings. Centroids of high intercolonial variance occured at and between cluster boundaries and were typical of transitions between, and rainfall-temperature discontinuities within, ecological-climatological zones, hence areas of ecological instability. Principal component and stepwise discriminant analysis yielded three morphometric clusters corresponding to A. m. sahariensis and A. m. intermissa in Morocco and to A. m. iberica (with three biometric populations) in Spain, but no pheromone clusters. The combined morphometric and pheromonal variance spectra indicated regions of natural hybridisation along a Sahara-Pyrenees transect. In the Horn of Africa, discrete and statistically homogeneous populations were identified: A. m. jemenitica, A. m. bandasii, A. m. sudanensis in Ethiopia and an unclassified group in southwestern Somalia. Areas of high intercolonial variance were interpreted as zones of hybridisation between the populations. Along a transect in west central Africa, three distinct homogeneous populations and two zones of hybridisation were found. These bees were designated as A. m. adansonii whose area of distribution was intruded by an un-named mountain group of bees and a third group, A. m. jemenitica. The delineation of the hybrid zones was supported by intercolonial variance spectra and these significant asymmetries were found to be coincident with transitions between the ecological-climatological zones. In southwestern Africa, two discrete homogeneous populations and a zone of hybridisation between them were identified: A. m. scutellata in northern South Africa and southern Namibia and A. m. adansonii in northern Namibia. Along a transect in the southeastern woodland savanna of Africa, three discrete populations were classified: A. m. litorea in Mozambique, A. m. scutellata in Zimbabwe and A. m. adansonii in northwestern Zambia. A zone of introgression between the last two subspecies occured in south-central Zambia and in the Zambezi valley

The use of a nonradioactive probe in RFLP analysis of Neurospora crassa DNA

Our laboratory is investigating the use of nonradioactive alternatives for the synthesis of DNA probes used in hybridization experiments

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

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