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The Geography of Phytochemical Races

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Chapter 4<br />

Intercontinental Disjunctions<br />

4.1 Across the Atlantic Ocean<br />

4.1.1 Datiscaceae<br />

Until comparatively recently, Datiscaceae were thought by some taxonomists<br />

(e.g., Cronquist, 1981), to consist <strong>of</strong> four species in three genera, the monospecifi<br />

c Octomeles (O. sumatrana Miq.) and Tetrameles (T. nudifl ora R. Br. ex Benn.)<br />

and Datisca. Octomeles and Tetrameles are large trees native to southeastern Asia;<br />

Datisca consists <strong>of</strong> D. cannabina L., which occurs from southwestern Asia to<br />

Crete, and D. glomerata (Presl) Baill., which occurs in California and northern Baja<br />

California, Mexico.<br />

Earlier work on the fl avonoid components <strong>of</strong> D. cannabina by Grisebach<br />

and Grambow (1968) and Pangarova and Zapesochnaya (1974) had revealed<br />

the existence <strong>of</strong> an unusual array <strong>of</strong> fl avonoids that included glycosides <strong>of</strong> the<br />

rare 3,5,7-trihydroxyfl avone galangin [299] and its 7-methyl ether [300], and<br />

3,5,7,2′-tetrahydroxyfl avone, datiscetin [301], and its 7-methyl ether [302] (see<br />

Fig. 4.1), along with the common fl avonols: kaempferol and quercetin. Since galangin<br />

and datiscetin, and their methyl ethers, represented unusual substitution patterns<br />

among the fl avonoids, it seemed reasonable to look at the other members <strong>of</strong> the<br />

putative family for their possible presence. A detailed study <strong>of</strong> D. glomerata showed<br />

that the unusual B-ring-substituted fl avonoids were indeed present as major components,<br />

whereas the Asian taxa exhibited only common glycosides <strong>of</strong> kaempferol and<br />

quercetin (Bohm, 1988). <strong>The</strong> fl avonoid pr<strong>of</strong>i le <strong>of</strong> D. glomerata was homogeneous.<br />

This is not the case with isozymes or chloroplast DNA.<br />

Despite the morphological similarity <strong>of</strong> D. cannabina and D. glomerata, and<br />

their distinctive fl avonoid pr<strong>of</strong>i les, an electrophoretic examination revealed an<br />

entirely different picture (Liston et al., 1989). Calculation <strong>of</strong> the mean genetic identity<br />

among populations <strong>of</strong> both species, based upon variation <strong>of</strong> enzymes coded for<br />

at 21 loci, yielded a value <strong>of</strong> I = 0.142. Intraspecifi c genetic identities were I = 0.649<br />

for D. cannabina and 0.847 for D.<br />

<strong>The</strong> authors suggested the following sequence <strong>of</strong> events as a possible explanation<br />

for the present-day distribution. It has been thought that the DG-S plastome,<br />

B.A. Bohm, <strong>The</strong> <strong>Geography</strong> <strong>of</strong> <strong>Phytochemical</strong> <strong>Races</strong>,<br />

© Springer Science+Business Media B.V. 2009<br />

173

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