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FIGURE 13.11 Diversity structure of 42 cultivated vanilla and Vanilla bahiana accessions and detailed relationships of the Polynesian accessions derived from neighbor joining trees using the distance matrix of Sokal and Michener (529 variables and 1000 bootstraps).

Some others cultivars were not discriminated by their AFLP pattern; this was the case of Tahiti and Haapape. Their morphological differences were unambiguous; nevertheless, their genetic diversity has been found to be only the consequence of the number of copies of each AFLP marker. For this reason, cytogenetic analyses were developed.

As previously described for V. planifolia by Nair and Ravindran (1994), all the cells of a single root do not present the same chromosome value for Tahitian vanilla. We also observed these variations for the accessions of V. planifolia and V. pompona. Three ploidy levels were observed among the Polynesian accessions. The chromosome counts for numerous metaphase plates of root tips, and the genome size measurements by flow cytometry were concordant. Three groups were distinguished:

1. A diploid group (2×) with chromosome number ranging from 22 to 31 and with a genome size from 4.87 to 5.80 pg. These characteristics concerned the majority of the Polynesian cultivars: Tahiti (Figure 13.12), Rea rea, Parahurahu, Oviri, Paraauti, Potiti, Puroini, Pupa, Popoti, and Poura.

2. A triploid group (3×) for which the chromosome number varies from 33 to 41. This group contains two sterile vanilla plants called “Haapape sterile” showing abnormal flower physiology (absence of pollen and autoincompatibility).

3. A tetraploid group (4×) where the number of chromosomes and the genome size are twice as high as in the first group (43–56 chromosomes and genome size of 10.10–10.89 pg). The following are the cultivars: Haapape, Ofe ofe, Tiarei, and Tahiti long.

FIGURE 13.12 Metaphase plates of (a) cultivar Tahiti with 24 chromosomes and (b) cultivar Haapape with 52 chromosomes.

Conclusion

The originality of Tahitian vanilla is due to its morphology, its texture, and the aromatic content of its pods. These characteristics are indeed related to genotype. They are also influenced by geographical areas of cultivation. For example, beans of Tahitian vanilla produced and cured in French Polynesia are different from those produced in other countries. The rare and highly considered gourmet French Polynesian spice results from a combination of the factors the soil, the climate, and also the Polynesian people, who carefully produce and cure the vanilla beans.

Acknowledgments

The authors thank Dr. S. Siljak-Yakovlev (Univ. Paris Sud) and Dr. S.C. Brown (CNRS Gif sur Yvette) for their help in cytogenetic analysis and for their interest and support to Tahitian vanilla genome studies, and J. Foster for his invaluable comments on the manuscript.

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