Use of Wing Geometric Morphometric Analysis and mtDNA to Identify Africanization of <i>Apis mellifera</i> in the Central Highlands of Ecuador
Diego Masaquiza,
Lino Curbelo Rodríguez,
José Zapata,
Joffre Monar,
Maritza Vaca,
Leonardo Porrini,
Martin Eguaras,
Martin Daniele,
Dora Romero,
Amilcar Arenal
Affiliations
Diego Masaquiza
Sede Orellana, Escuela Superior Politécnica de Chimborazo, El Coca 220150, Ecuador
Lino Curbelo Rodríguez
Center for Animal Development and Production Studies, Ignacio Agramonte Loynaz University of Camagüey, Camagüey 74650, Cuba
José Zapata
Sede Orellana, Escuela Superior Politécnica de Chimborazo, El Coca 220150, Ecuador
Joffre Monar
Sede Orellana, Escuela Superior Politécnica de Chimborazo, El Coca 220150, Ecuador
Maritza Vaca
Facultad de Ciencias Pecuarias, Escuela Superior Politécnica de Chimborazo, Riobamba 060106, Ecuador
Leonardo Porrini
Department of Biology, Faculty of Exact Sciences, National University of Mar del Plata, Mar del Plata 7600, Argentina
Martin Eguaras
Department of Biology, Faculty of Exact Sciences, National University of Mar del Plata, Mar del Plata 7600, Argentina
Martin Daniele
Sede Alto Valle y Valle Medio, Escuela de Veterinaria y Producción Agroindustrial, Universidad Nacional de Río Negro, Choele Choel 8360, Rio Negro, Argentina
Dora Romero
Laboratorio de Parasitología, Unidad de Diágnostico, Torreón del Molino, Facultad de Medicina Veterinaria y Zootecnia, Universidad Veracruzana, Veracruz 91697, Mexico
Amilcar Arenal
Department of Infectious Diseases and Pathology, School of Veterinary Medicine, St. Nicholas University, Morne Daniel, Roseau 00109-8000, Dominica
Seventy-five samples were collected from 15 beehives in the central highlands of Ecuador (Tungurahua–Chimborazo) to assess Africanization in managed bee populations using wing geometric morphometric and mitochondrial DNA analyses. The results indicated that when grouping the apiaries based on altitudinal floors into 2600–2800, 2801–3000, and 3001–3274 m above sea level, differences (p p Apis mellifera scutellata (D2 = 3.51), with 95.8% Africanization via father in the area. The maternal origin of all patterns belonged to lineage A (A. m. scutellata), with seven haplotypes. The most frequent haplotypes were A26 and A1; however, the A1q haplotype was not detected at the national level or in nearby countries. The identified haplotypes do not coincide with A4, which is predominant in South Africa and Brazil. The results indicate a double origin due to their presence in North Africa and the Iberian Peninsula. The formation of specific morphological groups within ecoregions is suggested.