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The Geography of Phytochemical Races

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2.7 North and Central America 103<br />

between desert and nondesert plants, however. With only one exception (fl ower buds<br />

from Anza-Borrego plants), tissues from desert plants had higher concentrations <strong>of</strong><br />

the glucosinolate than those from more moderate environments. Experiments with<br />

Isomeris grown under laboratory conditions revealed that glucocapparin content<br />

varied inversely with soil nitrogen, suggesting that the availability <strong>of</strong> this element<br />

in nature strongly infl uences the formation <strong>of</strong> the defense compound, which is in<br />

accord with the views <strong>of</strong> Coley et al. (1985) who hold that species that grow slowly<br />

owing to limitations <strong>of</strong> resources evolve “immobile defenses” (phenolic compounds<br />

or fi ber) whereas “mobile defenses” are produced by plants that are capable <strong>of</strong> rapid<br />

growth in the presence <strong>of</strong> ample resources. Isomeris arborea, which is capable <strong>of</strong><br />

rapid growth (Blua et al., 1988), falls within this latter category.<br />

2.7.13 Soils and Asters<br />

One <strong>of</strong> the earliest studies <strong>of</strong> variation involving fl avonoids was that <strong>of</strong> Abrahamson<br />

and Solbrig (1970) who examined these compounds, including an analysis <strong>of</strong> total<br />

anthocyanins, in several species <strong>of</strong> Aster along a transect running from extreme<br />

northwestern Pennsylvania to eastern Massachusetts. Soil and plant samples were<br />

taken from 19 sites. Soil samples were examined for a variety <strong>of</strong> features: nitrate<br />

content, moisture, color, and clay content. Plants were taken to the University <strong>of</strong><br />

Michigan Botanical Gardens where they were maintained in a uniform garden environment.<br />

Extracts <strong>of</strong> the cultivated plants were analyzed by paper chromatography<br />

and total anthocyanin (determined to be cyanin) content was determined colorimetrically.<br />

<strong>The</strong> species were identifi ed as A. ciliolatus Lindl. (two sites), A. cordifolius L.<br />

(12 sites), A. lowreianus Porter (one site), and A. undulatus L. (one site). Considerable<br />

variation was seen in the chromatographic pr<strong>of</strong>i les, with six compounds<br />

(spots, actually) common to all 83 plants, ten present in over 60 plants, and nine<br />

variable within populations. No compound (spot) was species specifi c. Anthocyanin<br />

concentration also varied without evident pattern. Likewise, there appeared<br />

to be no relationship between fl avonoid pr<strong>of</strong>i les and soil. Signifi cantly different<br />

chromatographic pr<strong>of</strong>i les were observed at different times throughout the growing<br />

season, which led the authors to caution future workers to be wary <strong>of</strong> randomly collected<br />

samples and to make use <strong>of</strong> common garden studies whenever possible. <strong>The</strong>ir<br />

advice has not always been followed.<br />

2.7.14 Lupinus sericeus (Fabaceae)<br />

In this example, individual plants <strong>of</strong> Lupinus sericeus Pursh were collected over a<br />

distance measuring approximately 1500 km, including most <strong>of</strong> the range <strong>of</strong> the species.<br />

In practice, this amounted to a north–south transect running from the Alberta-<br />

British Columbia border to northern Arizona. Lupinus sericeus occurs from southeastern<br />

British Columbia and southwestern Alberta to the Kaibab Plateau in northern Arizona,

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