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The Geography of Phytochemical Races

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2.3 Europe 49<br />

be more prevalent in southern areas than in more northerly sites; thus, Greenland,<br />

Iceland, and Norway had only two, fi ve, and one chemotype, respectively.<br />

<strong>The</strong> north–south gradient was also evident in the concentration <strong>of</strong> the most<br />

abundant chemotype, which was shown to consist <strong>of</strong> linaloöl [19] and its acetate.<br />

Most frequent in Greenland, Iceland, and Norway (90–100%), it was present<br />

in only 40% <strong>of</strong> plants collected in Scotland, and in only ca. 5% <strong>of</strong> plants<br />

from southern sites. This fi nding paralleled the observations <strong>of</strong> Stahl-Biskup and<br />

Laakso (1990) that a similar north–south trend exists in the oils <strong>of</strong> Thymus serpyllum<br />

subspecies serpyllum and tanaensis in Finland. <strong>The</strong> opposite trend was<br />

observed with γ-terpinene, which was present in southern populations but absent<br />

from those from the northern sites.<br />

Perhaps the most interesting aspect <strong>of</strong> this set <strong>of</strong> studies is the question posed<br />

in the recent paper by Schmidt et al. (2004) and deals with the reality <strong>of</strong> the<br />

patterns they observed. Is the polymorphism observed a result <strong>of</strong> the calculation<br />

methods used in the study, neural network (NN), and multivariate statistical<br />

analysis (MVA)? Would increased sampling result in a greater number <strong>of</strong> chemotypes?<br />

It is entirely possible, <strong>of</strong> course, that the numbers obtained in this study are<br />

a true refl ection <strong>of</strong> the biosynthetic capacities <strong>of</strong> the plants studied. <strong>The</strong> authors<br />

concluded—and this is a point made elsewhere in this review—that “. . . for a<br />

correct interpretation a good knowledge <strong>of</strong> the biosynthetic background <strong>of</strong> the<br />

components is needed.”<br />

2.3.12 Pinus uncinata (Pinaceae)<br />

Pinus uncinata Ram. occurs discontinuously from the north <strong>of</strong> Spain to western<br />

Switzerland, including populations in the Jura, the Vosges, and the Massif Central.<br />

Although the taxonomy <strong>of</strong> this species is evidently open to some discussion,<br />

Lauranson and Lebreton (1991) chose to set differences <strong>of</strong> opinion aside in their<br />

study <strong>of</strong> the fl avonoid pr<strong>of</strong>i les <strong>of</strong> this pine. (References to the taxonomic literature<br />

can be found in their paper.) For their fl avonoid analysis, twigs were collected<br />

from at least 23 individuals at each <strong>of</strong> fi ve locations, two in the Pyrenees,<br />

two in the Alps, and one in the Jura (Fig. 2.28). Site information, and relevant<br />

results <strong>of</strong> their analyses, appears in Table 2.9. Procyanidin and prodelphinidin<br />

(measured as the corresponding anthocyanidins, cyanidin [106], and delphinidin<br />

[107], respectively) were found to occur in the same ratio in each population.<br />

Following hydrolysis <strong>of</strong> the glycosidic fraction, three fl avonols were identifi ed,<br />

kaempferol [108], quercetin [109], and isorhamnetin [110] (See Fig. 2.29 for<br />

structures 106–110). Statistical analysis revealed that the fi ve populations could<br />

be discriminated by their respective quercetin contents. <strong>The</strong> individuals from<br />

each population were sorted into three categories: (1) less than 10% quercetin;<br />

(2) 10–16% quercetin; and (3) more than 16% quercetin. Based upon the assumption<br />

that the quercetin concentration was under one locus-two allele (A and a)<br />

genetic control and that the three genotypes, AA, Aa, and aa, represented high,

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