GENETIC-VARIABILITY AND GENE FLOW IN GEOGRAPHICAL POPULATIONS OF CERATITIS-CAPITATA (WIED) (MEDFLY)

被引:56
作者
GASPERI, G
GUGLIELMINO, CR
MALACRIDA, AR
MILANI, R
机构
[1] UNIV PAVIA, DIPARTIMENTO GENET & MICROBIOL, I-27100 PAVIA, ITALY
[2] CNR, IST GENET & BIOL EVOLUZ, PAVIA, ITALY
关键词
CERATITIS-CAPITATA; ELECTROPHORETIC MARKERS; GENE FLOW; GENETIC VARIABILITY; GEOGRAPHICAL POPULATIONS;
D O I
10.1038/hdy.1991.98
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Two African populations of Ceratitis capitata (Kenya and Reunion Isl.) and two Mediterranean ones (Sardinia and Procida Isl.) have been studied for genetic variability at 25 loci by electrophoresis. Wright's F(ST), Slatkin's Nm* gene flow estimator, Nei's distance (D) together with measures of variability such as HBAR, PBAR, ABAR have been used to compare the population from Kenya with the other three. Parameters using gene frequencies (F(ST), D, Nm*) indicate the presence of substantial geographic heterogeneity, largely attributable to genetic drift and correlated with dispersion of the medfly from its source area (Subsaharan Africa) to the periphery. The Kenyan population has high genetic variability (assessed by HBAR, PBAR AND ABAR), as might be expected given its native status. Significant gene flow estimates between Kenya and the derived Mediterranean populations supports the hypothesis of recent colonization. Part of the geographic heterogeneity is related to the presence of fixed alleles in the more differentiated Reunion population although it maintains the genetic attributes of the ancestral population. Selection or other forces may have played an important role in the differentiation of this population.
引用
收藏
页码:347 / 356
页数:10
相关论文
共 32 条
[1]  
[Anonymous], 1976, HDB ENZYME ELECTROPH
[2]  
ASPERI G, 1987, FRUIT FLIES, P149
[3]  
BERLOCHER SH, 1984, EVOLUTION, V38, P906, DOI 10.1111/j.1558-5646.1984.tb00361.x
[4]  
Fletcher B.S., 1989, FRUIT FLIES THEIR B, P195
[5]  
Gasperi G., 1986, P153
[6]  
GASPERI G, 1990, GENETIC SEXING MEDIT, P90
[7]  
GILLESPIE JH, 1974, GENETICS, V76, P837
[8]  
HAGEN KS, 1981, REPORTS PROGR RES, V35, P5
[9]  
HUETTEL MD, 1980, GENETICS, V94, P47