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The Geography of Phytochemical Races

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6.6 Ullung Island, Korea 275<br />

Pointing in that direction is the recent study <strong>of</strong> ITS sequences in Carmichaelia,<br />

Clianthus, Montigena, and Swainsonia, four genera that comprise Carmichaelinae<br />

(Wagstaff et al., 1999). [Those authors provided a node-based defi nition and recommended<br />

that the clade be recognized as subtribe Carmichaelinae.] Briefl y, their data<br />

suggest an origin <strong>of</strong> Carmichaelinae from a North American ancestor (from Astragalinae)<br />

with subsequent diversifi cation into several lineages, one <strong>of</strong> which was<br />

Carmichaelia. This divergence was thought to have accompanied the increased aridity<br />

in Australia and New Zealand during the Tertiary. Carmichaelia fi rst appears in<br />

the fossil record in the late Pliocene Waipaoa Series (Oliver, 1928). Of interest to us<br />

here is the fi nding that ITS information places the Lord Howe Island taxon, C. exsul,<br />

in the midst <strong>of</strong> a group <strong>of</strong> nine species, which, interestingly, includes C. kirkii, whose<br />

fl avonoid chemistry was commented upon above. Wagstaff et al. (1999) suggest<br />

that dispersal to Lord Howe Island has occurred “recently,” but did not provide an<br />

estimate <strong>of</strong> the time involved, other than to comment on the age <strong>of</strong> the island.<br />

6.6 Ullung Island, Korea<br />

6.6.1 Acer (Sapindaceae)<br />

Ullung Island (or Ulleung-do) is a small, volcanic island lying in the Sea <strong>of</strong> Japan,<br />

approximately 150 km east <strong>of</strong> Korea and 300 km west <strong>of</strong> Japan at 37°30′N, 130°50′E.<br />

<strong>The</strong> island has an area <strong>of</strong> only about 73 km 2 and has been available for colonization<br />

by propagules for an estimated 1.8 million years (B.-Y. Sun and Stuessy,<br />

1998). Species belonging to 34 genera (25 families) are endemic to the island. Two<br />

endemic members <strong>of</strong> Acer, A. okamotanum Nakai and A. takesimense Nakai, have<br />

been examined using both micro- and macromolecular methods. Morphological<br />

data suggest that these two species have been derived from two different ancestors.<br />

ITS data (Cho et al., 1996) confi rm this suggestion. Acer okamotanum is thought<br />

to be closely related to A. mono Maxim., and thus could have arisen from ancestral<br />

stock from either Korea or Japan. A close relationship between A. takesimense and<br />

A. pseudosieboldianum (Pax) Kom., based on morphological features, is strongly<br />

supported by the lack <strong>of</strong> ITS sequence divergence. It is interesting to note that<br />

Chang and Giannasi (1991), studying fl avonoids <strong>of</strong> Acer sect. Palmata, suggested<br />

that A. takesimense and A. pseudosieboldianum might be better treated as conspecifi<br />

c. Sun and Stuessy (1998) discuss other endemic taxa <strong>of</strong> Ullung Island.<br />

6.6.2 Cotoneaster wilsonii (Rosaceae)<br />

Cotoneaster wilsonii Nakai, endemic to Ullung Island, is one <strong>of</strong> the many species<br />

<strong>of</strong> the genus that occur in eastern Asia. <strong>The</strong> fl avonoid pr<strong>of</strong>i le <strong>of</strong> this species consists

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