Abstract:-The genetic structure of the Iberian honey bee (Apis mellifera iberiensis) was studied by analysing 10 microsatellite loci in 362 workers representative of nine Spanish provinces. Heterozygosity values of Iberian honeybee populations are intermediate between African and west European ones whereas allelic diversity is remarkably high at several loci. There is no definite geographic structure of Iberian honeybee populations. At a peninsular scale, the expected clinal pattern observed with mitochondrial data has… Show more
“…We noticed that over half of all HNHK individuals were of the CH (13/30) and hybrid (5/30) types (Supplementary file 4; Figure 1b). Similar introgression has been reported in A. mellifera populations Cánovas et al 2011). The unusual Hainan race is particularly sensitive to such introgression owing to its narrow distribution and limited population size.…”
-In this study, we reexamined the patterns of divergence and phylogeographic structure among Apis cerana populations on Hainan island and southern mainland China. Analysis of 10 microsatellite loci from 12 geographically distinct A. cerana populations identified a total of 151 alleles, with a range of 7 to 24 at each locus. The level of genetic variation (observed heterozygosity) within each population ranged from 0.603 to 0.661, while variation within populations contributed most (93.78-98.84 %) of the molecular variance. Microsatellite data revealed three differentiated groups, one including all the mainland populations while the other two containing one of and the other three island populations, respectively. Severe genetic introgressions from mainland China into Hainan island were apparent, and these were characterized at both population and individual levels using combined analysis of microsatellites and mitochondrial DNA.Apis cerana / microsatellite / phylogeographic structure / genetic introgression
“…We noticed that over half of all HNHK individuals were of the CH (13/30) and hybrid (5/30) types (Supplementary file 4; Figure 1b). Similar introgression has been reported in A. mellifera populations Cánovas et al 2011). The unusual Hainan race is particularly sensitive to such introgression owing to its narrow distribution and limited population size.…”
-In this study, we reexamined the patterns of divergence and phylogeographic structure among Apis cerana populations on Hainan island and southern mainland China. Analysis of 10 microsatellite loci from 12 geographically distinct A. cerana populations identified a total of 151 alleles, with a range of 7 to 24 at each locus. The level of genetic variation (observed heterozygosity) within each population ranged from 0.603 to 0.661, while variation within populations contributed most (93.78-98.84 %) of the molecular variance. Microsatellite data revealed three differentiated groups, one including all the mainland populations while the other two containing one of and the other three island populations, respectively. Severe genetic introgressions from mainland China into Hainan island were apparent, and these were characterized at both population and individual levels using combined analysis of microsatellites and mitochondrial DNA.Apis cerana / microsatellite / phylogeographic structure / genetic introgression
“…For example, Kandemir et al (2006) detected two distinct mitochondrial lineages C and O, although the overall Cyprus population was relatively homogenous in terms of microsatellites. Similar disagreement between mitochondrial and nuclear markers occurs in Africanized honey bees (Lobo 1995) and in A. m. iberica (Cánovas 2008(Cánovas , 2011. In studies of subspecies identification, it was recommended to use mtDNA only for initial screening (Rortais et al 2011) or together with morphometrics or nuclear markers (Nielsen et al 1999;Pinto et al 2003).…”
-Identification of honey bee (Apis mellifera) subspecies is important for their protection. It is also used by queen breeders to maintain some breeding lines. In this study, we compared three methods of subspecies identification based on the following: 17 microsatellite loci, COI-COII mitotypes and geometric morphometrics of forewing venation. The methods were used to classify colonies and workers from a mixed population of A. m. mellifera and A. m. carnica. There was highly significant correlation between results obtained using the three methods. More than three quarters of colonies were classified to the same subspecies by all three methods. The agreement was highest between microsatellites and morphometrics. More than 90 % of colonies were classified to the same subspecies by the two methods. There was also relatively high agreement (75 %) between microsatellites and morphometrics when workers were classified as pure subspecies or hybrids. In particular, one pure subspecies was never misclassified as other pure subspecies. The results presented here show that morphometrics can be used for detection of hybrids between A. m. mellifera and A. m. carnica. geometric morphometrics / subspecies discrimination / microsatellites / mtDNA / Bayesian clustering / Apis mellifera / phenotype-genotype correlation
“…According to Cánovas et al. (, ), the North African honey bees (A lineage) have colonized southwest of Europe (M lineage) and there was hybridization between lineages. Our results confirm this finding because on the neighbor‐joining phylogenetic tree, the H4, H13, H14 from Spain and H20 (Melli4) were closely related with the M lineage, and the H17 and H19 (Iberi2) also from Spain had closer connection with the A lineage (Fig.…”
Carniolan honey bees (Apis mellifera carnica) are considered as an indigenous subspecies in Hungary adapted to most of the ecological and climatic conditions in this area. However, during the last decades Hungarian beekeepers have recognized morphological signs of the Italian honey bee (Apis mellifera ligustica). As the natural distribution of the honey bee subspecies can be affected by the importation of honey bee queens or by natural gene flow, we aimed at determining the genetic structure and characteristics of the local honey bee population using molecular markers. All together, 48 Hungarian and 84 foreign (Italian, Polish, Spanish, Liberian) pupae and/or workers were used for mitochondrial DNA analysis. Additionally, 53 sequences corresponding to 10 subspecies and the Buckfast hybrid were downloaded from GenBank. For the nuclear analysis, 236 Hungarian and 106 foreign honey bees were genotyped using nine microsatellites. Heterozygosity values, population‐specific alleles, FST values, principal coordinate analysis, assignment tests, structure analysis, and dendrograms were calculated. Haplotype and nucleotide diversity values showed moderate values. We found that one haplotype (H9) was dominant in Hungary. The presence of the black honey bee (Apis mellifera mellifera) was negligible, but a few individuals resembling other subspecies were identified. We proved that the Hungarian honey bee population is nearly homogeneous but also demonstrated introgression from the foreign subspecies. Both mitochondrial DNA and microsatellite analyses corroborated the observations of the beekeepers. Molecular analyses suggested that Carniolan honey bee in Hungary is slightly affected by Italian and black honey bee introgression. Genetic differences were detected between Polish and Hungarian Carniolan honey bee populations, suggesting the existence of at least two different gene pools within A. m. carnica.
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