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The Geography of Phytochemical Races

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5.1 Vascular Plants 219<br />

in the graphing <strong>of</strong> values seen in Fig. 5.1. <strong>The</strong> correlation <strong>of</strong> evolutionary advancement<br />

values, without reference to individual taxa, indicates that the European taxa<br />

have substitution patterns most closely resembling the base structures, the Australian<br />

specimens are a little more complex (advanced, specialized?), and the Asian and<br />

North American taxa display highly derived B- and A-rings, respectively. This in turn<br />

suggests that the xanthone containing Gentianaceae originated in temperate Europe,<br />

and their spread into new areas was accompanied by structural changes associated<br />

with one ring or the other.<br />

Other examples in the Gottlieb and Kubitzki (1983) paper, following similar<br />

statistical methodology and logic, concern chemical changes in the evolution <strong>of</strong><br />

Aniba (Lauraceae) in the Amazon, and associated river basins; and relationships<br />

among genera <strong>of</strong> Papilionoideae as a function <strong>of</strong> their accumulated alkaloids. <strong>The</strong>se<br />

are complex examples that would repay careful study by interested readers.<br />

5.1.3 Hordeum (Poaceae)<br />

Hordeum vulgare L. and several closely related species have been important elements<br />

in agriculture for a very long time. Mabberley (1997, p. 346) informs us that barley<br />

was fi rst harvested some 11,000 years ago. In the 1960s, Fröst and his colleagues<br />

undertook studies <strong>of</strong> the fl avonoids <strong>of</strong> barley and its relatives as a possible source <strong>of</strong><br />

information in tracking routes <strong>of</strong> movement <strong>of</strong> this valuable food plant (Fröst and<br />

Asker, 1973, 1977; Fröst and Holm, 1971, 1972, 1977; Fröst et al., 1975, 1977). <strong>The</strong><br />

early survey studies revealed the existence <strong>of</strong> three clear-cut chemical races—called<br />

A, B, and C—based upon their fl avonoid spot pr<strong>of</strong>i les. Analysis <strong>of</strong> 1424 local varieties<br />

was made, along with samples <strong>of</strong> H. spontaneum and H. agriocrithon (Fröst and<br />

Holm, 1975). Chemotypes A and B (there was further differentiation <strong>of</strong> type B into<br />

two subforms but this fact does not infl uence the overall picture) were observed in<br />

varieties from throughout much <strong>of</strong> the world, including collections made in Europe,<br />

Asia, the Middle East, Africa, and North America. Race C, on the other hand, was<br />

observed primarily in varieties collected in Ethiopia (238 <strong>of</strong> 279 varieties tested).<br />

<strong>The</strong>se workers surmised that race C had evolved from race B, followed by selection.<br />

Structural studies <strong>of</strong> the fl avonoids revealed the pr<strong>of</strong>i les to consist <strong>of</strong> O- and<br />

C-glycosyl derivatives <strong>of</strong> the common fl avones, apigenin, luteolin, and chrysoeriol.<br />

<strong>The</strong> bulk <strong>of</strong> the variation observed results from the nature <strong>of</strong> the sugar attached to the<br />

6-C-glucosyl fl avones (Fröst et al., 1977).<br />

5.1.4 Pteridium aquilinum sens. lat. (Pteridaceae)<br />

<strong>The</strong> toxic properties <strong>of</strong> Pteridium aquilinum L., the common bracken fern, have<br />

been known to humankind for a very long time. Two principal causes <strong>of</strong> trouble are<br />

its carcinogenic properties (M. Saito et al., 1975; I. A. Evans, 1976; Hirono, 1986)

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