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The Geography of Phytochemical Races

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14 2 Examples Within Continents<br />

(4) a group consisting <strong>of</strong> limonene and α-pinene as codominant constituents. <strong>The</strong><br />

northern-most region was dominated by a race, represented by six sites, in which<br />

citronellal was the major component, with concentrations ranging from 36.98% to<br />

62.24% (Ave. = 48.32%). No other site yielded oil with higher than 25.63% citronellal.<br />

<strong>The</strong> southernmost race (six sites) had limonene as the dominant terpene, with<br />

concentrations falling in the range 43.18–56.92% (Ave. = 49.91%). <strong>The</strong> highest concentration<br />

<strong>of</strong> limonene observed otherwise was 42.98% in one <strong>of</strong> the codominant<br />

races. Populations in the middle <strong>of</strong> the range <strong>of</strong> this species tended to exhibit mixed<br />

terpene compositions. <strong>The</strong> workers concluded that the citronellal race should best<br />

be considered as an ecotype that has only recently evolved, a view supported in<br />

fl oral bud and leaf morphology.<br />

2.2.2 Duboisia myoporoides (Solanaceae)<br />

<strong>The</strong> genus Duboisia consists <strong>of</strong> three species limited in occurrence to eastern Australia<br />

(Fig. 2.6) and parts <strong>of</strong> New Guinea. Duboisia myoporoides R. Br., the taxon <strong>of</strong> interest<br />

to us in the present context, is solely Australian in its occurrence. Evidence for the<br />

existence <strong>of</strong> chemical variation within the species was fi rst described by L<strong>of</strong>tus Hills<br />

et al. (1953, 1954) who observed that scopolamine [26] (see Fig. 2.7 for structures<br />

26–30) was the dominant alkaloid in plants collected north <strong>of</strong> Gosford, New South<br />

Wales, whereas hyoscyamine [27] was the dominant alkaloid in collections south <strong>of</strong><br />

Gosford. (Gosford, NSW, lies roughly between Newcastle and Sydney at 33°25′S,<br />

151°18′E.) Later, a third variant was discovered in a region known as the Acacia<br />

Plateau, near Killarney, Queensland (southwest <strong>of</strong> Brisbane), that was characterized<br />

by the possession <strong>of</strong> the pyridine-based alkaloids, nicotine [28] and anabasine [29]<br />

(see also Mortimer and Wilkinson, 1957). Other minor components reported, according<br />

to Gritsanapan and Griffi n (1991), included valeroidine, valtropine, tigloidine,<br />

tropine, butropine, norscopoline, poroidine, isoporoidine, acetyltropine, aposcopolamine,<br />

noratropine, atropine, and tetramethylputrescine. None <strong>of</strong> these appears to<br />

fi gure signifi cantly in the geographic patterning.<br />

<strong>The</strong> most recent work, by Gritsanapan and Griffi n (1991), extended the range <strong>of</strong><br />

study to more northerly sites in Queensland and included populations at different<br />

elevations. Four sites were studied: (1) northern Queensland at elevation 1000 m;<br />

(2) near Tinaroo Dam on the Atherton Plateau (near Cairns, Qld.) at 2200 m;<br />

(3) Mt. Glorious (near Brisbane) at 700 m; and (4) a revisited site at Acacia Plateau<br />

at an elevation <strong>of</strong> about 1000 m. Scopolamine was the major alkaloid present in<br />

plant material from Tinaroo Dam, from Mt. Glorious, and from coastal northern<br />

Queensland. Accompanying scopolamine in the Mt. Glorious plants were nicotine<br />

and anabasine. Plants from Acacia Plateau yielded a small amount <strong>of</strong> scopolamine,<br />

which was the only tropane alkaloid detected, but major quantities <strong>of</strong> nicotine,<br />

anabasine, and hygrine [30]. Hygrine was also observed as a lesser component <strong>of</strong><br />

plant material from the Mt. Glorious site. It is instructive to recognize that hygrine,<br />

or a biologically active form there<strong>of</strong>, lies on the biosynthetic pathway leading to the

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