RESUMEN
The aim of this study was to analyse the level and structure of genetic and morphometric variation in the East-Central European populations of Phengaris (Maculinea) nausithous. On the basis of the life cycle of the species, we expected a low level of variation within the populations coupled with a relatively high level of differentiation among them. We also assumed that the differentiation among the populations has a regional pattern. In order to confirm these assumptions, we collected population samples from two regions within the Carpathian Basin (western Transdanubia and Transylvania) and from a region east of the Carpathian Mountains (Bukovina). The level of enzyme polymorphism and the amount of morphometric variation were investigated in the sampled populations. As the western (Transdanubia) and the eastern populations (Transylvania plus Bukovina) were suggested to belong to different subspecies (Rákosy et al. in Nota Lepidopterol 33:31-37, 2010), our working hypothesis was that these two groups of populations belong to different evolutionary significant units (ESUs). The results of all genetic analyses (PCA, Bayesian-clustering analysis and especially the UPGMA dendrogram) confirmed our assumption. The level of differentiation was higher between the western and eastern populations resulting in two monophyletic lineages of Phengaris (Maculinea) nausithous in East-Central Europe. This result suggests that these lineages can be considered as two different ESUs.
Asunto(s)
Evolución Biológica , Teorema de Bayes , Europa (Continente)RESUMEN
Nearly all of the known populations of Scarce Fritillary, Euphydryas maturna (Linnaeus, 1758), are declining in Western and Central Europe. In order to identify the possible reasons for its vulnerability we surveyed the population genetics of this butterfly species using multi-locus genotype data. Females of our target species lay lots of eggs in one or two batches only and pre-hibernation caterpillars live and feed gregariously in a nest. As a consequence, a random unfavourable event can eliminate most offspring of a particular female resulting in a strong genetic drift effect combined with inbreeding. Thus, our hypothesis regarding the genetic composition of Scarce Fritillary populations suggests that: (1) there will be random fluctuations in allele frequencies from generation to generation; (2) populations should exhibit small effective sizes and a relatively high level of heterozygote deficiency, and; (3) the majority of the individuals in a population will be composed of the offspring of just a few females. In order to test these hypotheses, fine-scale genetic structure was studied in two subpopulations of a Hungarian Scarce Fritillary population for 4 consecutive years (generations) using enzyme polymorphism data. The results supported all of our assumptions. We detected random fluctuation in the frequency of several alleles, small effective population size and the index of heterozygote deficiency (F IS) indicated a considerable level of inbreeding in most samples. Furthermore, average values of relatedness were also fairly high, and we were able to identify 17 putative sib families in total with the two subpopulations based on estimation of individual gametic phases. Thus, the present study suggests that intrinsic factors (e.g. specific life history) might increase the sensitivity of a species to various threatening factors (e.g. habitat loss or fragmentation) and result in the vulnerability of the given species.
Asunto(s)
Mariposas Diurnas/genética , Enzimas/genética , Variación Genética , Proteínas de Insectos/genética , Alelos , Animales , Mariposas Diurnas/enzimología , Ecosistema , Especies en Peligro de Extinción , Femenino , Frecuencia de los Genes , Flujo Genético , Genética de Población , Genotipo , Geografía , Hungría , RumaníaRESUMEN
Enzyme activity variation was studied in a Drosophila melanogaster population from two villages (Tiszafüred and Tiszaszolos) in Hungary. Two habitats (distillery and farmyard) were sampled in both villages and 8-9 isofemale lines were established from each sample with a total of 35 lines. The activities of ADH, alphaGPDH, IDH and 6PGDH were determined on starch gel after electrophoresis in 10 F1 females of each of the 35 isofemale lines. Three sublines were established from three selected isofemale lines of all four samples (altogether 36 sublines). Alcohol tolerance of the adult flies was assayed in these sublines. The activity of ADH was similar in the two habitats; so was the sensitivity to ethanol. Accordingly, no differences in adaptation to environmental ethanol were detected between the two habitats. The deviations between the two habitats in average activities and in the total variation of enzyme activities were not consistent in the two villages. These results suggest that founder effects and genetic drift are more pronounced in distilleries than selection. The association among enzyme activities varied greatly both between the two villages and between the two habitats. The two parameters of alcohol tolerance were not significantly different between the two habitats in any of the two villages.
Asunto(s)
Oxidorreductasas de Alcohol/metabolismo , Proteínas de Drosophila/metabolismo , Drosophila melanogaster/enzimología , Ambiente , Etanol/metabolismo , Glicerolfosfato Deshidrogenasa/metabolismo , Isocitrato Deshidrogenasa/metabolismo , Fosfogluconato Deshidrogenasa/metabolismo , Alcohol Deshidrogenasa , Animales , Cruzamientos Genéticos , Drosophila melanogaster/genética , Electroforesis en Gel de Almidón , Femenino , Efecto Fundador , Flujo GenéticoRESUMEN
Enzyme activity variation was assessed in several isofemale lines originating from two Hungarian Drosophila melanogaster populations. Samples from each population were taken from from two villages; 8-9 isofemale lines were established from each village. The activities of ADH, alphaGPDH, IDH and 6PGDH were determined in the adults (in the F1 generation) and in the larvae (in the F3 generation) as well. Enzyme activities were measured on starch gel after electrophoresis. The activity of the enzyme was detected in a single individual and it was also possible to determine its genotype. The results showed that most of the variation occurred within sites for all four enzymes. This within site variation was more or less equally partitioned into within and between isofemale line (family) components. A smaller portion of variation was attributable to the differences between the populations. Nevertheless, adult alphaGPDH, and larval IDH and 6PGDH activities exhibited significant differences between the two populations. Variation in larval activities of all enzymes was higher than that of the adults, but 6PGDH had considerably higher variation in the adults. The greater variation in larval activities probably reflected the greater environmental variation in the microhabitat of the larvae compared to that of the adults. Larval activities of the investigated enzymes showed much stronger correlation than adult activities. The correlation pattern in the adults differed greatly between the two populations.