‘Bruno’ ( A. deliciosa ) may have lower chilling requirements ( Caldwell, 1989 ). However, information has not been reported about the chilling requirements of other kiwifruit cultivars, especially for the new released cultivars with diverse ploidy levels
The usefulness of isozyme banding patterns as genetic markers in kiwifruit [Actinidia deliciosa (A. Chev.) C.F. Liang et A.R. Ferguson] was investigated using starch gel electrophoresis. Fifty-four entries putatively belonging to seven female and two male kiwifruit cultivars were examined for 13 enzyme systems (AAT, ACO, GDH, G6PDH, IDH, MDH, ME, MNR, NDH, 6PGD, PGI, PGM, and SKDH). Four enzyme systems, ACO, MDH, NDH, and SKDH, showed identical banding patterns in all clones surveyed. Of the remaining enzymes, AAT, PGI, and PGM had the best discriminating power. Six enzyme systems (GDH, G6PDH, IDH, ME, MNR, and 6PGD), though showing polymorphic banding patterns, were poorly resolved. All the New Zealand cultivars were uniquely identified by the simultaneous comparison of the AAT, PGI, and PGM zymograms. Some enzyme systems were also polymorphic among plants within the same cultivar, thus proving the heterogeneity of kiwifruit material introduced into Europe in the early 1970s.
several fruit quality attributes and nutritional status of the kiwifruit cultivar Tsechelidis. Materials and Methods The research was conducted in a commercial kiwifruit [ Actinidia deliciosa (A. chev.) C.F. Liang et A.R. Ferguson var. deliciosa
Forty-eight kiwifruit cultivars and selections, representing more than 90% of total world kiwifruit production, were investigated using nine SSR markers to establish genetic identities, and evaluate genetic diversity and relatedness. These nine SSRs were polymorphic and a total of 213 alleles were detected, resulting in a mean number of 23.7 alleles per locus, ranging from nine to 38 alleles. One hundred and thirty-three alleles were found to be common to both A. chinensis and A. deliciosa, while 33 and 36 were specific to A. chinensis and A. deliciosa, respectively. In addition, 34 alleles were specific to one single genotype and provided a set of valuable alleles for cultivar identification. A single SSR locus UDK 96-414 could differentiate all 48 genotypes except two presumable clones. Mean number of alleles per locus (A), percentage of polymorphic loci (P), and direct count heterozygosity (Ho) assessed for each genotype over all loci revealed considerable differences among these 48 genotypes. On average, A = 2.6, P = 89.4% and Ho = 0.546 were found in A. chinensis cultivars, while A = 3.5, P = 97.0% and Ho = 0.671 in A. deliciosa cultivars. Consensus fingerprint profiling using SSR markers is a useful and reliable method for establishing genetic identities of kiwifruit cultivars and selections. It also improves evaluation effectiveness of genetic diversity and relatedness compared to RAPD markers.
We investigated the characterization of genotypes of Actinidia deliciosa (Chev.) Liang and Ferguson var. deliciosa by using isozymatic and molecular techniques [randomly amplified polymorphic DNA (RAPD), amplified fragment-length polymorphism (AFLP), standard AFLP, and modified AFLP]. Four genotypes were tested, the female cultivar `Hayward', the traditional New Zealand pollinizers `Matua' and `Tomuri', and a new pollinizer named clone A selected in a breeding program in Spain. PGI and PGM were the only isozymes that allowed us to distinguish the kiwifruit genotypes, although the accessions of `Matua' presented two different banding patterns for both isozymes. All three molecular markers differentiated between the genotypes of kiwifruit tested, although RAPD markers did not allow us to establish differences between accessions of `Matua', while both standard and modified AFLP did. These results, along with those of isozymes, support the hypothesis that the male kiwifruit genotypes present in Europe belong to different clones. None of the markers used showed differences between accessions of `Hayward', which would suggest that it is a uniform cultivar. On the other hand, clone A was a seedling derived from `Hayward' and an unknown pollinizer. The results obtained using AFLP markers strongly suggest that `Tomuri' may have been the male parent of clone A. A specific protocol for kiwifruit characterization based on a modified AFLP technique is also presented, that gave rise to the highest percentage of polymorphism while scoring the lowest number of bands. This, together with the technical features of modified AFLP markers, make them very useful for identifying propagated kiwifruit plant material in commercial nurseries.
of both species, it would be expected that relative cold tolerance between these species would vary considerably by cultivar. Kiwifruit are functionally dioecious, with segregation ratios for sex among seedlings reportedly expected to have a 1:1 ratio
particularly the genetic factors ( Wang and Cao, 1996 ). Not only different species, but also different cultivars of the same species present variations in their antioxidant profile. For example, a recent study has shown that the apple cultivar may
on the prices obtained for the fresh fruit. Factors influencing fruit price include total supply, season of supply, cultivar and, most important, fruit quality. Fruit quality in kiwifruit has many components such as fruit size, shape, flesh texture
‘Jinyan’, a kiwifruit cultivar selected and promoted by the Wuhan Botanical Garden, Chinese Academy of Sciences during the last decade, is one the most promising gold-fleshed cultivars for the south of China. It is thought to be an interspecific
kiwifruit cultivars at Chilton Research and Extension Center in Thorsby, AL, 2005. ‘Golden Dragon’ and ‘Golden Sunshine’ had the lowest chilling requirements for flowers, at 800 h and 850 h, respectively. ‘Golden Dragon’ and ‘Golden Sunshine’ may be