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690 IRIDACEAE/IRIS<br />

LOUISIANA IRISES are rhizoma<strong>to</strong>us, have laterally compressed (flat-appearing) leaves and beardless<br />

falls, and are very variable in color. Hybridization, including introgressive hybridization (=<br />

hybridization resulting in movement <strong>of</strong> genes from one species <strong>to</strong> ano<strong>the</strong>r), in LOUISIANA IRISES<br />

has been studied in detail and has been argued <strong>to</strong> be <strong>of</strong> long-term evolutionary significance<br />

(e.g., Anderson 1949; Arnold et al. 1990a, 1990b, 1991, 1992; Nason et al. 1992; Arnold 1993; Arnold<br />

& Wesselingh 2000). Pollination in IRISES: each petal-like style branch is opposite one <strong>of</strong><br />

<strong>the</strong> three outer perianth segments (= sepals ) and <strong>the</strong>re is a stamen between it and <strong>the</strong> sepal. The<br />

sepals typically act as landing platforms for pollinating insects such as bees. On <strong>the</strong> underside<br />

<strong>of</strong> each style branch, near <strong>the</strong> apex, is a little flap <strong>of</strong> tissue whose upper surface is sticky—this is<br />

<strong>the</strong> stigma. When an insect (presumably carrying pollen) lands on one <strong>of</strong> <strong>the</strong> sepals, it starts <strong>to</strong><br />

crawl in between <strong>the</strong> sepal and <strong>the</strong> adjacent style branch in search <strong>of</strong> nectar. In <strong>the</strong> process, it<br />

makes contact with <strong>the</strong> sexual organs <strong>of</strong> <strong>the</strong> flower. As <strong>the</strong> pollina<strong>to</strong>r enters <strong>the</strong> constricted<br />

space, it brushes against <strong>the</strong> flap <strong>of</strong> stigmatic tissue which is pulled downward <strong>to</strong> expose <strong>the</strong><br />

sticky stigmatic surface. As a result, pollen on <strong>the</strong> insect’s body is rubbed <strong>of</strong>f on<strong>to</strong> <strong>the</strong> sticky receptive<br />

surface <strong>of</strong> <strong>the</strong> stigma. In addition, pollen from <strong>the</strong> adjacent an<strong>the</strong>r is deposited on<strong>to</strong> <strong>the</strong><br />

insect’s body during its foraging for nectar. When <strong>the</strong> pollinating insect exits <strong>the</strong> reproductive<br />

area <strong>of</strong> <strong>the</strong> flower (carrying <strong>the</strong> flower’s pollen), <strong>the</strong> little flap <strong>of</strong> stigmatic tissue is moved back<br />

upward, which is thought <strong>to</strong> prevent self-pollination (Faegri & van der Pijl 1979; Mabberley<br />

1997). IRISES are also known <strong>to</strong> produce self-incompatible pollen, which promotes cross-pollination<br />

and prevents self-fertilization. “Asexual reproduction in many Iris species may be more<br />

important than sexual reproduction in <strong>the</strong>ir persistence, and many hybrid clones may persist<br />

for decades in sites no longer cultivated” (Henderson 2002). The common name FLAG is derived<br />

from <strong>the</strong> Middle English flakken, <strong>to</strong> flutter, in reference <strong>to</strong> fluttering in <strong>the</strong> wind (Durant 1976).<br />

(Named after Iris, Greek goddess <strong>of</strong> <strong>the</strong> rainbow, from <strong>the</strong> varied flower colors)<br />

REFERENCES: Dykes 1913; Anderson 1936, 1949; Foster 1937; Riley 1938; Arnold et al. 1990a,<br />

1990b, 1991, 1992, 1993; Ma<strong>the</strong>w 1990; Henderson 1992, 1994, 2002; Nason et al. 1992; Arnold<br />

1993, 1994; Cruzan et al. 1993; Species Group <strong>of</strong> <strong>the</strong> British Iris Society 1997; Arnold &<br />

Wesselingh 2000; Caillet et al. 2000.<br />

1. Leaves nearly cylindrical, channeled on upper surface; plant with a bulb ______________________ I. xiphium<br />

1. Leaves laterally compressed, appearing � flat, <strong>the</strong> two surfaces identical; plant with a thick rhizome.<br />

2. Perianth dark red <strong>to</strong> reddish brown, coppery brown, orange, or yellow (without blue or purple<br />

coloration when fresh, but sometimes drying with purple areas); sepals (= falls) without a<br />

beard (= hairy patch).<br />

3. Perianth bright yellow <strong>to</strong> golden yellow; fruits 3-angled; petals (= standards) much<br />

shorter than sepals ________________________________________________________ I. pseudacorus<br />

3. Perianth dark red <strong>to</strong> reddish brown, coppery brown, or orange; fruits 6 angled; petals<br />

nearly as long as sepals (but narrower) _______________________________________________ I. fulva<br />

2. Perianth bluish, purplish, or white (or variously colored in cultivated forms); sepals without an<br />

obvious beard OR with a beard <strong>of</strong> multicellular hairs.<br />

4. Sepals with a beard <strong>of</strong> multicellular hairs; petals (= standards) 30–60 mm wide; introduced<br />

species.<br />

5. Spa<strong>the</strong>s entirely scarious (= dry, papery, and translucent or transparent) and silvery white<br />

at flowering time, 20–35 mm long; perianth tube 8–13 mm long ______________________ I. pallida<br />

5. Spa<strong>the</strong>s scarious in <strong>the</strong> upper half, <strong>the</strong> lower half greenish, sometimes with purplish<br />

tinge at base at flowering time, 35–55 mm long; perianth tube 17–25 mm long _______ I. germanica<br />

4. Sepals without an obvious beard (but can have very short pubescence); petals 10–30 mm<br />

wide; native species.<br />

6. Cauline leaf immediately subtending spa<strong>the</strong>s usually shorter than <strong>to</strong> slightly longer than<br />

<strong>the</strong> spa<strong>the</strong>s or absent; stems nearly as long as or longer than <strong>the</strong> basal leaves, not zigzag;<br />

ovaries and fruits 3-angled ________________________________________________ I. virginica

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