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Material and methods

Six wheat-Aegilops ovata hybrid lines derived from the BC3F3-population of the Triticum aestivum Chinese Spring x Aegilops ovata amphiploid (Ganeva et al. 1992) were studied. Both parents were also included. The excess Cu tolerance was assessed at seedling stage at two concentrations of Cu ions in CuSO4 solution (CuSO4.8H2O): 10-6 M and 10-5 M. Plant growth was estimated by measuring the length and fresh weight of roots, shoots and the whole plant. To measure tolerance the tolerance index (TI) was calculated as a ratio: growth in metal solution / growth in control solution (water) (Macnair 1993). Chromosome counts and arm ratio measurements were made in root tip cells on N-banded chromosome spreads. N-banding was conducted according to Gill et al. (1991).


Results and discussion

The roots length reduction in Aegilops ovata was significantly less than in Chinese Spring at both low and high Cu concentrations (
Fig. 1). There was no significant difference between the two parental genotypes regarding the shoots growth at concentration of 10-6 M. At the higher concentration the performance of Chinese Spring was better.

The performance of two of lines, ADL-18 and ADL-33, was better at both concentrations of Cu ions in comparison with the, parents and the rest of lines. They combined the better roots growth of the wild species with the better shoots growth of 'Chinese Spring' at stress conditions (
Fig. 1).

The chromosome N-banding analysis showed that both tolerant lines, ADL-18 (2n=40+4t) and ADL-33 (2n=40+3t) carry one and the same pair of submetacentric (arm ratio 2.45) Aegilops ovata chromosomes substituted for wheat D-genome chromosomes (
Fig. 2). The N-banded karyotype of the parental Aegilops ovata accession is given for comparison (Fig. 3). The rest of lines do not carry this alien chromosome. The telocentrics are supposed to be the short and the long arm of wheat chromosome 4A, which is missing in the complement of both lines. The comparison with the C-banded (Friebe et al. 1995) and N-banded (our unpublished results) chromosomes of the U- genome donor, Aegilops umbellulata, suggests that the alien chromosome pair is 3U (Fig. 3). Studies on the genetical control of mineral stress tolerance indicated the major effect of homoeologous groups 5 and 2 chromosomes in the members of Triticeae (Manyowa and Miller 1991). The role of group 3 chromosomes has also been reported. Aluminum tolerance has been transferred into bread wheat through chromosome 3N of Aegilops uniaristata (Miller et al. 1992). Modifying genes for excess boron tolerance were found on chromosome 3R in rye, 3S in Aegilops sharonensis and 3E in Agropyron elongatum (Manyowa 1989, cited in Manyowa and Miller 1991). We suppose that the Aegilops ovata chromosome 3U contribute to the excess Cu tolerance through its effect on the growth of roots. In wheat, the effect of group 3 chromosomes on root development has been established (Sears .1954). Both ADL-18 and ADL-33 lines had slower root growth in control solution compared with the rest of lines and the parents (data not shown). This opinion is also in agreement with the observation that in most cases tolerant ecotypes have slower growth than the typical non-tolerant ones (Macnair 1993).

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