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The Geography of Phytochemical Races

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38 2 Examples Within Continents<br />

naturally in Lithuania. Although differentiation <strong>of</strong> chemotypes was indicated by the<br />

data, the relevant observation noted by the authors (Mockute and Judzentiene, 2003)<br />

is the existence <strong>of</strong> different chemical pr<strong>of</strong>i les, Portugal, Norway, and a population<br />

from Estonia in one, another population from Estonia comprising a second, and<br />

populations from Canada comprising yet another. Important leads to the literature<br />

can be found in the Lithuanian work.<br />

2.3.6 Pulicaria dysenterica (Asteraceae)<br />

Recent work on fl avonoids <strong>of</strong> Pulicaria dysenterica (L.) Bernh. fi ts in well at this<br />

point since it too exhibits variation in the expression <strong>of</strong> O-methylated fl avonols<br />

(Williams et al., 2000). In addition to the use <strong>of</strong> this plant in folk medicine formalized<br />

in its specifi c epithet, its common name in English, “fl eabane,” gives recognition<br />

to its value as an agent to discourage fl eas and other insects from taking up<br />

residence in human quarters. Interest in the fl avonoid chemistry <strong>of</strong> fl eabane led<br />

to the discovery, as by the cited workers, <strong>of</strong> several chemotypes involving plants<br />

collected from different places in England and continental Europe. Whereas<br />

the vacuolar fl avonoid pr<strong>of</strong>i le, consisting <strong>of</strong> just quercetin 3-O- glucuronide,<br />

was observed in all specimens, the leaf exudate fractions showed differences in<br />

major components. Four chemical variants were observed based upon the major<br />

(or in some cases sole) fl avonol derivative(s): (1) quercetagetin 3,7-dimethyl<br />

ether [74]; (2) 6-hydroxykaempferol-3,4′-dimethyl ether [75]; (3) a mixture <strong>of</strong><br />

6-hydroxykaempferol-3,7-dimethyl ether [76] and quercetagetin 3,7,3′-trimethyl<br />

ether [77]; and (4) a mixture <strong>of</strong> 6-hydroxykaempferol-3,7-dimethyl ether, quercetagetin<br />

3,7,3′-trimethyl ether, and quercetagetin 3,7,3′,4′-tetramethyl ether [78]<br />

(see Fig. 2.19 for structures 74–78). It is diffi cult to assess the signifi cance <strong>of</strong><br />

these chemical variants owing to limited sampling and the possibility that they<br />

are responding to some environmental factor or factors. Common garden studies<br />

coupled with more extensive collections are necessary to put the existence <strong>of</strong><br />

these forms on fi rm ground. Additional variation was noted with reference to the<br />

work <strong>of</strong> Pares et al. (1981) who reported quite a different fl avonoid pr<strong>of</strong>i le from<br />

material collected in Turkey.<br />

2.3.7 Thalictrum minus (Ranunculaceae)<br />

This example demonstrates how widely chemical pr<strong>of</strong>i les can differ between two<br />

populations separated by only a matter <strong>of</strong> kilometers; in this case, populations <strong>of</strong><br />

halictrum minus L. in the Vojvodina area <strong>of</strong> Serbia (Popovic et al., 1992) (Fig. 2.20).<br />

Plants collected at 500 m in the Fruska Gora Mountains (Novi Sad) afforded a<br />

comparatively complex mixture <strong>of</strong> benzylisoquinoline alkaloids that consisted <strong>of</strong>

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