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Apis Mellifera L. (api + mellifera_l)
Selected AbstractsTHE AFRICANIZATION OF HONEYBEES (APIS MELLIFERA L.) OF THE YUCATAN: A STUDY OF A MASSIVE HYBRIDIZATION EVENT ACROSS TIMEEVOLUTION, Issue 7 2002Kylea E. Clarke Abstract Until recently, African and European subspecies of the honeybee (Apis mellifera L.) had been geographically separated for around 10,000 years. However, human-assisted introductions have caused the mixing of large populations of African and European subspecies in South and Central America, permitting an unprecedented opportunity to study a large-scale hybridization event using molecular analyses. We obtained reference populations from Europe, Africa, and South America and used these to provide baseline information for a microsatellite and mitochondrial analysis of the process of Africanization of the bees of the Yucatan Peninsula, Mexico. The genetic structure of the Yucatecan population has changed dramatically over time. The pre-Africanized Yucatecan population (1985) comprised bees that were most similar to samples from southeastern Europe and northern and western Europe. Three years after the arrival of Africanized bees (1989), substantial paternal gene flow had occurred from feral Africanized drones into the resident European population, but maternal gene flow from the invading Africanized population into the local population was negligible. However by 1998, there was a radical shift with both African nuclear alleles (65%) and African-derived mitochondria (61%) dominating the genomes of domestic colonies. We suggest that although European mitochondria may eventually be driven to extinction in the feral population, stable introgression of European nuclear alleles has occurred. [source] TEMPORAL PATTERN OF AFRICANIZATION IN A FERAL HONEYBEE POPULATION FROM TEXAS INFERRED FROM MITOCHONDRIAL DNAEVOLUTION, Issue 5 2004M. Alice Pinto Abstract The invasion of Africanized honeybees (Apis mellifera L.) in the Americas provides a window of opportunity to study the dynamics of secondary contact of subspecies of bees that evolved in allopatry in ecologically distinctive habitats of the Old World. We report here the results of an 11-year mitochondrial DNA survey of a feral honeybee population from southern United States (Texas). The mitochondrial haplotype (mitotype) frequencies changed radically during the 11-year study period. Prior to immigration of Africanized honeybees, the resident population was essentially of eastern and western European maternal ancestry. Three years after detection of the first Africanized swarm there was a mitotype turnover in the population from predominantly eastern European to predominantly A. m. scutellata (ancestor of Africanized honeybees). This remarkable change in the mitotype composition coincided with arrival of the parasitic mite Varroa destructor, which was likely responsible for severe losses experienced by colonies of European ancestry. From 1997 onward the population stabilized with most colonies of A. m. scutellata maternal origin. [source] THE AFRICANIZATION OF HONEYBEES (APIS MELLIFERA L.) OF THE YUCATAN: A STUDY OF A MASSIVE HYBRIDIZATION EVENT ACROSS TIMEEVOLUTION, Issue 7 2002Kylea E. Clarke Abstract Until recently, African and European subspecies of the honeybee (Apis mellifera L.) had been geographically separated for around 10,000 years. However, human-assisted introductions have caused the mixing of large populations of African and European subspecies in South and Central America, permitting an unprecedented opportunity to study a large-scale hybridization event using molecular analyses. We obtained reference populations from Europe, Africa, and South America and used these to provide baseline information for a microsatellite and mitochondrial analysis of the process of Africanization of the bees of the Yucatan Peninsula, Mexico. The genetic structure of the Yucatecan population has changed dramatically over time. The pre-Africanized Yucatecan population (1985) comprised bees that were most similar to samples from southeastern Europe and northern and western Europe. Three years after the arrival of Africanized bees (1989), substantial paternal gene flow had occurred from feral Africanized drones into the resident European population, but maternal gene flow from the invading Africanized population into the local population was negligible. However by 1998, there was a radical shift with both African nuclear alleles (65%) and African-derived mitochondria (61%) dominating the genomes of domestic colonies. We suggest that although European mitochondria may eventually be driven to extinction in the feral population, stable introgression of European nuclear alleles has occurred. [source] Long-range foraging by the honey-bee, Apis mellifera L.FUNCTIONAL ECOLOGY, Issue 4 2000M. Beekman Abstract 1.,Waggle dances of honey-bees (Apis mellifera L.) were decoded to determine where and how far the bees foraged during the blooming of heather (Calluna vulgaris L.) in August 1996 using a hive located in Sheffield, UK, east of the heather moors. The median distance foraged was 6·1 km, and the mean 5·5 km. Only 10% of the bees foraged within 0·5 km of the hive whereas 50% went more than 6 km, 25% more than 7·5 km and 10% more than 9·5 km from the hive. 2.,These results are in sharp contrast with previous studies in which foraging distances were much closer to the hive. In May 1997 the mean foraging distance was 1 km, showing that long-range dancing is not the rule in Sheffield. 3.,The observed foraging distances described in this study may not be exceptional in a patchy environment where differences in patch size and patch quality are large. When travel distances to patches are large, distant patches can probably be utilized only by individuals that live in groups and recruit foragers to the patches found. Only then are the benefits of scouting for distant patches high enough to enable the exploitation of these patches. [source] Effect of triflumuron on brood development and colony survival of free-flying honeybee, Apis mellifera L.JOURNAL OF APPLIED ENTOMOLOGY, Issue 4 2004O. G. Amir Abstract:, The effect of the insect growth regulator (IGR) triflumuron (Alsystin® 25 WP) on honeybee, Apis mellifera L. (Hym., Apidae), was studied in a semi-field test. Free-living colonies were fed one litre per hive of sucrose syrup containing 0, 0.025, 0.25 or 2.5 g of triflumuron. A significant reduction in flight activity was noted 6,10 weeks post-treatment at the two higher doses. These colonies reared less brood than before treatment. While the comb area occupied by uncapped brood was as high as [0.025 and 0.25 g active ingredient (a.i.)] or higher (2.5 g a.i.) than before treatment, there was a significant decline in capped brood at the two higher doses, indicating enhanced larval mortality. No capped brood was reared in the hive treated at the highest dose from 3,9 weeks post-treatment. Yet there was a significant accumulation of pollen and honey in the brood compartment at all doses. All colonies except the one treated at the highest dose survived the following winter. However, at 43 weeks post-treatment, hives treated at intermediate and low doses showed a significant increase in uncapped brood and a significant decrease in capped brood. This study revealed a strong residual toxicity of triflumuron to brood and substantiated its classification as hazardous to honeybee. [source] Origin of honeybees (Apis mellifera L.) from the Yucatan peninsula inferred from mitochondrial DNA analysisMOLECULAR ECOLOGY, Issue 6 2001Kylea E. Clarke Abstract Honeybees (Apis mellifera L.) sampled at sites in Europe, Africa and South Ámerica were analysed using a mitochondrial DNA restriction fragment length polymorphism (RFLP) marker. These samples were used to provide baseline information for a detailed analysis of the process of Africanization of bees from the neotropical Yucatan peninsula of Mexico. Radical changes in mitochondrial haplotype (mitotype) frequencies were found to have occurred in the 13-year period studied. Prior to the arrival of Africanized bees (1986) the original inhabitants of the Yucatan peninsula appear to have been essentially of southeastern European origin with a smaller proportion having northwestern European ancestry. Three years after the migration of Africanized bees into the area (1989), only very low levels of maternal gene flow from Africanized populations into the resident European populations had occurred. By 1998, however, there was a sizeable increase in the proportion of African mitotypes in domestic populations (61%) with feral populations having 87% of mitotypes classified as African derived. The results suggest that the early stages of Africanization did not involve a rapid replacement of European with African mitotypes and that earlier studies probably overestimated the prevalence of African mitotypes. [source] Five hundred and fifty microsatellite markers for the study of the honeybee (Apis mellifera L.) genomeMOLECULAR ECOLOGY RESOURCES, Issue 2 2003Michel Solignac Summary Microsatellites are currently considered the most useful genetic markers with wide applications in genomics, quantitative and population genetics. We present here the structure of the core sequence of 552 microsatellites, together with the sequences of the primers and the length of the sequenced allele. These microsatellites were isolated from several libraries constructed from either fractions of total genomic DNA or from clones of a bacterial artificial chromosome (BAC) library. All 552 loci are polymorphic in the honeybee. Many of them were also successfully amplified in three other species of Apis: A. cerana (58%), A. dorsata (59%) and A. florea (38%). A summary of the variability of 36 loci in the three main evolutionary lineages of A. mellifera is given. [source] Potential effects of tyramine on the transition to reproductive workers in honeybees (Apis mellifera L.)PHYSIOLOGICAL ENTOMOLOGY, Issue 2 2007KEN SASAKI Abstract To explore the role of brain tyramine in reproductive worker honeybees, its effects after injection and oral treatment on brain dopamine levels and ovarian development in queenless worker honeybees are determined. Both tyramine injection and oral treatment in 10-day-old queenless bees leads to tyramine transportation into the brain and significantly elevates brain dopamine levels as a function of the tyramine concentration. Ovarian diameters are significantly larger in 10-day-old queenless bees treated with tyramine compared with queenless bees of the same age without tyramine treatment. Results on yolk formation in the ovary support the finding of increased ovarian diameter, suggesting that oral tyramine treatment accelerates ovarian development through dopamine effects and/or direct effects of tyramine on the ovary in queenless bees. Thus, tyramine has potential effects on the enhancement of brain dopamine levels and the acceleration of ovarian development for the transition of normal workers to reproductive worker honeybees. [source] Potential mechanism for detection by Apis mellifera of the parasitic mite Varroa destructor inside sealed brood cellsPHYSIOLOGICAL ENTOMOLOGY, Issue 3 2002Caroline Martin Abstract The parasitic mite Varroa destructor Anderson & Trueman is a major pest of the honeybee Apis mellifera L. throughout the world. Chemical agents currently used for mite control leave contaminating residues and promote pesticide resistance. As an alternative means of control, it would be useful to identify natural substances enabling bees to detect Varroa inside brood cells. These substances could then be used to trigger mite hygienic behaviour by bees. In this study several techniques were used to screen substances that might allow detection of infested brood cells by bees. Gas chromatography-mass spectrometry analysis was performed on substances extracted in dichloromethane from the contents of brood cells. Solid phase microextraction and solid injection were performed on substances obtained from living and dead Varroa, respectively. Electroantennography was performed to assess the sensitivity of olfactory receptors in bee antennae to some of these substances. Principal component analysis based on proportions of cuticular substances allowed discrimination between bees and other cell contents. Foundress Varroa exhibited the greatest dissimilarity to healthy pupae that were used as controls. Immature Varroa and faecal material were intermediate. High molecular weight compounds, mainly dimethylalkanes, were proportionally the most characteristic components of foundress Varroa. This finding suggests that these compounds would be the most apt to induce uncapping of cells infested by Varroa. Solid-phase microextraction and solid injection demonstrated the presence of aliphatic acids, esters, and one alcohol, eicosenol, in Varroa. Electroantennographic recordings showed that mite-resistant bees were more responsive to some acids and one ester. We speculate that these compounds may be involved in recognition of living Varroa by honeybees. [source] Impacts of hive honeybees on Tasmanian leatherwood Eucryphia lucida Labill. (Eucryphiaceae)AUSTRAL ECOLOGY, Issue 2 2009STEPHEN A. MALLICK Abstract Despite honeybees (Apis mellifera L.) occurring as a feral and commercially managed species in many parts of Australia, the effects of honeybees on native Australian ecosystems are poorly understood. We examined the impacts of honeybee apiaries on Tasmanian Leatherwood Eucryphia lucida Labill. (Eucryphiaceae) by comparing commercial apiary sites with control sites >2 km from the nearest apiary. Feral honeybees were common at control sites (73% of honeybees feral) but were scarce at apiary sites (2%), and hive honeybees appeared to be competitively displacing feral honeybees near apiaries. Visit rates by native insects appeared to be un-affected by the increased numbers of hive honeybees near apiaries. Standing crops of nectar sugar were significantly depressed at apiary sites. Pollen was rapidly removed from flowers at apiary sites resulting in full separation of the male and female flower-phases (flowers completely dichogamous). In contrast, at control sites, pollen tended to remain in flowers into the female phase (flowers partially dichogamous). There was no difference in the total number of pollen grains deposited on stigmas or in percentage seed set among apiary and control sites. However, fruit set was elevated at apiary sites, possibly owing to reduced autonomous (within-flower) selfing. Our study indicated that honeybees significantly reduce floral resources (nectar and pollen) around apiaries, although any competitive effects on native insects may have been obscured by large variation in the abundance of native insects among experimental sites. [source] Lipid-enhanced pollen and lipid-reduced flour diets and their effect on the longevity of honey bees (Apis mellifera L.)AUSTRALIAN JOURNAL OF ENTOMOLOGY, Issue 3 2007Rob Manning Abstract, As eucalypt pollens contain low concentrations of lipid, enhancing pollen diets with fatty acids was hypothesised to improve honey bee longevity. Different concentrations of linoleic and oleic acid added to eucalypt pollen were trialled in small cages containing approximately 1400 bees each. Bees fed diets of redgum (Corymbia calophylla (Lindl.) Hill & Johnson, formerly Eucalyptus calophylla) pollen had the lowest mortality of 22 diets tested for 6 weeks and had life spans (50%) greater than 42 days. Linoleic acid mixed with a redgum diet in concentrations >6% corresponded to life spans of 24,25 days. Bee longevity appeared to be more sensitive to oleic acid as life spans decreased to 15,21 days when diets had concentrations >2%. The life spans of bees fed soya bean flour were 26 days on low (0.6% lipid) fat, 19 days on defatted and 20 days on full-fat diets. Bees fed lupin flour had a life span of 23 days. Adding redgum pollen to lupin flour caused increased mortality, but addition of pollen to soya bean flour was beneficial. Thus, beekeepers who choose to utilise soya bean or lupin flours as protein substitutes to pollen will have bees with reduced longevity. Bees fed redgum pollen that had been dried, crushed, irradiated and hermetically stored in a cool room for several years had similar longevity to bees fed fresh-collected and frozen redgum pollen. [source] | |||||||||||||||||||||||||