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Journal Article

Genetic Analysis of a Hybrid Zone Between the Fire-Bellied Toads, Bombina bombina and B. variegata, Near Cracow in Southern Poland

Jacek M. Szymura and Nicholas H. Barton
Evolution
Vol. 40, No. 6 (Nov., 1986), pp. 1141-1159
DOI: 10.2307/2408943
Stable URL: http://www.jstor.org/stable/2408943
Page Count: 19

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Topics: Clines, Hybridity, Alleles, Enzymes, Genetic loci, Gene flow, Genetics, Toads, Linkage disequilibrium, Genotypes
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Since scans are not currently available to screen readers, please contact JSTOR User Support for access. We'll provide a PDF copy for your screen reader.
Genetic Analysis of a Hybrid Zone Between the Fire-Bellied Toads, Bombina bombina and B. variegata, Near Cracow in Southern Poland
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Abstract

The fire-bellied toads Bombina bombina and B. variegata differ extensively in biochemistry, morphology, and behavior. We use a survey of five diagnostic enzyme loci across the hybrid zone near Cracow in Southern Poland to estimate the dispersal rate, selection pressures, and numbers of loci which maintain this zone. The enzyme clines coincide closely with each other and with morphological and mitochondrial DNA clines. Although the zone lies on a broad transition between environments suitable for bombina and variegata, the close concordance of diverse characters, together with increased aberrations and mortality in hybrids, suggest that the zone is maintained largely by selection against hybrids. There are strong "linkage disequilibria" between each pair of (unlinked) enzyme loci (R̄ = 0.129 [2-unit support limits: 0.119-0.139]). These are probably caused by gene flow into the zone, and they give an estimate of dispersal (σ = 890 [790-940] m gen-1/2). The clines are sharply stepped, with most of the change occurring within 6.15 (5.45-6.45) km, but with long tails of introgression on either side. This implies that the effective selection pressure on each enzyme marker (due largely to disequilibrium with other loci) is s* = 0.17 (0.159-0.181) at the center but that the selection acting directly on the enzyme loci is weak or zero (se < 0.0038). The stepped pattern implies a barrier to gene flow of 220 (48-415) km. This would substantially delay neutral introgression but would have little effect on advantageous alleles; the two taxa need not evolve independently. Strong selection is needed to maintain such a barrier: hybrid populations must have their mean fitness reduced by a factor of 0.65 (0.60-0.77). This selection must be spread over a large number of loci to account for the concordant patterns and the observed cline widths (N = 300 [80-2,000]).

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