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The Geography of Phytochemical Races

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5.2 Nonvascular Plants 243<br />

present, as well as in their structure, although all compounds from this taxon were<br />

based upon the same fundamental carbon skeleton. Compounds obtained from the<br />

upper tidal sites were shown to be debromoisolarinterol [506], debromoaplysin<br />

[507], α-bromocuparene [508], the ether [509], and the newly described cuparene<br />

derivative, isolaurenisol [510]. Plants from the lowest site afforded only two compounds,<br />

isolaurinterol [511] and allolaurinterol [512] (see Fig. 5.14 for structures<br />

506–518). Cholesterol was identifi ed from plants collected at all sites. It is tempting<br />

to speculate that the presence <strong>of</strong> some herbivore living at lower depths has driven<br />

selection <strong>of</strong> a different set <strong>of</strong> compounds that serve as feeding deterrents in this part<br />

<strong>of</strong> the alga’s range. An alternative explanation, which ought to be borne in mind with<br />

all <strong>of</strong> these chemically differentiated populations, is that one is dealing with cryptic<br />

species. It would be <strong>of</strong> interest to combine the study <strong>of</strong> chemicals, chromosome<br />

structure and number, life cycle features, and, ideally, some gene-sequence studies,<br />

on some system <strong>of</strong> this sort in order to determine how useful, or reliable, the secondary<br />

chemistry might be.<br />

On the basis <strong>of</strong> morphological and secondary metabolic differences, Masuda et al.<br />

(1997c) concluded that an alga previously known as Laurencia obtusa (Hudson)<br />

Lamouroux var. snackeyi (Weber-van Bosse) Yamada (earlier name was L. paniculata<br />

Fig. 5.14 Compounds 506–518, more terpenes from Laurencia species

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