Krigia occidentalis |
Krigia |
|||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
western dwarfdandelion |
dwarf dandelion |
|||||||||||||||||||||||||
Habit | Annuals, 4–16 cm; taprooted. | Annuals or perennials, 3–75 cm; taprooted, fibrous-rooted, or (in K. dandelion) with rhizomes bearing globose tubers. | ||||||||||||||||||||||||
Stems | 1–20+, ± scapiform, erect, eglandular or lightly glandular-villous. |
1–50+, usually erect, rarely decumbent, scapiform or branched distally, glabrous or sparingly villous (proximally), glandular-villous (especially distally). |
||||||||||||||||||||||||
Leaves | basal (rosettes) and proximally cauline (on scarcely elongated branches close to ground); petiolate (petioles sometimes ciliate-glandular); blades linear, oblanceolate, or obovate, 1–7 cm, margins entire or sparingly lobed, lobes linear or triangular to rounded, apices acute or obtuse, faces eglandular. |
mostly basal, sometimes cauline; petiolate (petioles often winged); blades linear to lanceolate, oblanceolate, or spatulate, margins entire, denticulate, or irregularly pinnately lobed, apices acute to obtuse (faces glabrous or glandular-villous, usually glaucous in K. dandelion and K. biflora); distal cauline usually slightly reduced to bractlike. |
||||||||||||||||||||||||
Peduncles | from basal rosettes. |
not distally inflated, ebracteate (from rosettes and from axils of cauline leaves or bracts). |
||||||||||||||||||||||||
Involucres | 2.5–6.5 mm. |
turbinate to campanulate, 2–12 mm diam. |
||||||||||||||||||||||||
Receptacles | flat or low-convex, pitted, glabrous, epaleate. |
|||||||||||||||||||||||||
Florets | 5–25; corollas yellow, 5–9 mm. |
5–60; corollas yellow to orange (equaling or surpassing phyllaries). |
||||||||||||||||||||||||
Phyllaries | 4–7, erect in fruit, lanceolate in flower, becoming ovate-lanceolate in fruit, midveins and sometimes secondary veins becoming prominent in fruit, curving inward at bases to form keels, apices acute. |
(4–)5–18 in 1–2 series, (sometimes reflexed in fruit) linear-lanceolate to ovate, equal, herbaceous, apices acute (faces glabrous). |
||||||||||||||||||||||||
Calyculi | 0. |
|||||||||||||||||||||||||
Heads | borne singly. |
borne singly. |
||||||||||||||||||||||||
Cypselae | reddish brown, broadly obconic, 1.2–1.8 mm (apical areas broader than basal areoles), 10–15-ribbed; pappi of 5, hyaline, rounded outer scales 0.4–0.6 mm plus usually 5, sometimes 0, scabrous inner bristles 1.2–2 mm. |
brown or reddish brown, columnar, obconic, barrel-shaped, or fusiform, not beaked, nerves or ribs 10–20, glabrous; pappi 0, or persistent, often fragile, usually in 2 series, distinct, outer of 5+, yellowish or brownish scales, inner of 5–45, barbellulate bristles (pappi 0 in K. cespitosa, 0 or 1 series of tiny scales in K. wrightii). |
||||||||||||||||||||||||
x | = (4) 5 (6, 9). |
|||||||||||||||||||||||||
2n | = 12. |
|||||||||||||||||||||||||
Krigia occidentalis |
Krigia |
|||||||||||||||||||||||||
Phenology | Flowering Mar–Jun. | |||||||||||||||||||||||||
Habitat | Sandy or clay soils, meadows, prairies, edges of open oak-hickory and pine woods | |||||||||||||||||||||||||
Elevation | 10–400 m (0–1300 ft) | |||||||||||||||||||||||||
Distribution |
AR; GA; KS; LA; MO; OK; TX
|
North America; ne Mexico |
||||||||||||||||||||||||
Discussion | Krigia occidentalis grows in the Eastern deciduous forest biome, tallgrass prairie, and mixedgrass prairie. It has superficial similarity in pappus form to K. virginica; it was consistently placed as the sister species to K. cespitosa in chloroplast cpDNA and nuclear rDNA studies by K. J. Kim et al. (1992b, 1992c). In morphology, it is most similar to the polyploid species K. wrightii, with 2n = 18. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 7 (7 in the flora). Krigia is diverse and limited to North America. On molecular evidence, it stands apart from other clades of Cichorieae and is best placed as a monotypic subtribe (J. Lee et al. 2003; Lee and B. G. Baldwin 2004). Early studies classified the pappose and epappose species as different genera. A unified view of the genus was taken by L. H. Shinners (1947), and this has been supported by recent morphologic and molecular studies (K. J. Kim and T. J. Mabry 1991; Kim and B. L. Turner 1992; Kim et al. 1992b, 1992c; Kim and R. K. Jansen 1994). The most common base number is x = 5, with lower and higher numbers having arisen through dysploidy, autoploidy, and both ancient and recent alloploidy (K. L. Chambers 1965, 2004; A. S. Tomb et al. 1978; C. C. Chinnappa 1981; Kim and Turner). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
||||||||||||||||||||||||
Key |
|
|||||||||||||||||||||||||
Source | FNA vol. 19, p. 365. | FNA vol. 19, p. 362. | ||||||||||||||||||||||||
Parent taxa | Asteraceae > tribe Cichorieae > Krigia | Asteraceae > tribe Cichorieae | ||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||
Synonyms | Cymbia occidentalis | Apogon, Cymbia, Cynthia, Serinia, Troximon | ||||||||||||||||||||||||
Name authority | Nuttall: J. Acad. Nat. Sci. Philadelphia 7: 104. (1834) | Schreber: Gen. Pl. 2: 532. (1791) | ||||||||||||||||||||||||
Web links |