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The Geography of Phytochemical Races

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174 4 Intercontinental Disjunctions<br />

Fig. 4.1 Compounds<br />

299–302, fl avonoids from<br />

Datisca<br />

considered the ancestral type from phylogenetic analyses, was widely distributed<br />

throughout the range <strong>of</strong> the species in pre-Pleistocene times. Climatic cooling<br />

would have resulted in retreat <strong>of</strong> the species south <strong>of</strong> the Transverse Ranges but<br />

with localized populations surviving north <strong>of</strong> the Transverse Ranges. <strong>The</strong> existence<br />

<strong>of</strong> relictual populations in Monterey and Santa Cruz Counties would be consistent<br />

with the existence <strong>of</strong> other relictual taxa in suitable habitats in that area (Raven and<br />

Axelrod, 1978). A northern population that survived the climatic changes could<br />

have become fi xed for unique chloroplast DNA mutations and given rise to the<br />

present populations by range extension. <strong>The</strong> existence <strong>of</strong> the DG-N’ population in<br />

Mendocino County attests to the potential for differentiation within the northern<br />

form. <strong>The</strong> authors also pointed out that the differentiation <strong>of</strong> these two forms may<br />

have occurred several million years ago and in fact have nothing to do with Pleistocene<br />

climate extremes.<br />

A comparison <strong>of</strong> the cpDNA data for D. cannabina and D. glomerata revealed a<br />

sequence divergence <strong>of</strong> 0.87% ± 0.17%, which Liston et al. (1992) translated into a divergence<br />

time <strong>of</strong> 8.7 million years (± 1.7 million years) placing the divergence in the<br />

late Miocene. Sampling <strong>of</strong> D. cannabina was not suffi cient to allow further speculation<br />

on the relationship between the two species. <strong>The</strong> authors noted in their concluding<br />

remarks that this pair <strong>of</strong> species represents another system where genetic differentiation<br />

has occurred with comparatively little accompanying morphological change.<br />

4.1.2 Armeria maritima (Plumbaginaceae)<br />

This example involves Armeria maritima (Mill.) Willd., which is distributed over<br />

central and coastal Europe, Great Britain, and parts <strong>of</strong> North America. Attempts<br />

to accommodate the amount <strong>of</strong> variation that characterizes this taxon are refl ected<br />

in the existence <strong>of</strong> several infraspecifi c taxa, among which are subsp. maritima<br />

native to the coasts <strong>of</strong> Europe from northern Spain to Norway, subsp. calaminaria<br />

(Petri) Rothm. that appears principally in metalliferous surroundings, such as mine<br />

tailings; subsp. sibirica (Tuscz ex Boiss.) Nyman that occurs in the Arctic and in<br />

subarctic areas; and subsp. californica (Boiss.) Posild. Areas <strong>of</strong> occurrence <strong>of</strong> these<br />

subspecies are not necessarily contiguous as indicated by specimens <strong>of</strong> subsp.

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