Pectis longipes |
Pectis ×floridana |
|
---|---|---|
longstalk chinchweed, longstalk cinchweed, mat cinchweed |
chinchweed |
|
Habit | Perennials, 8–25 cm (rhizomes branched, 1–10 mm diam.); herbage lemon-scented or spicy-scented. | Annuals, 5–30 cm; herbage spicy-scented. |
Stems | ascending to erect (very leafy), glabrous. |
decumbent to erect, glabrous. |
Leaves | linear to linear-oblanceolate, 10–55 × 1–3 mm, margins with 1–4 pairs of setae, faces glabrous (conspicuously dotted on margins with round oil-glands 0.3–0.5 mm). |
linear, 15–35 × 1–2 mm, margins with 3–5 pairs of setae, faces glabrous (abaxial densely dotted with round oil-glands ca. 0.2 mm). |
Peduncles | (30–)50–160 mm. |
5–25 mm. |
Involucres | campanulate. |
cylindric to narrowly fusiform. |
Ray florets | (8–)13(–15); corollas 8–12 mm. |
5; corollas 3.5–4.2 mm. |
Disc florets | 25–50; corollas 4–6 mm (2-lipped). |
4–6; corollas 2.2–2.5 mm (2-lipped). |
Phyllaries | distinct, linear, linear-oblanceolate, or linear-elliptic, 5–8 × 0.7–2 mm (dotted with 1–3, swollen, subterminal oil-glands 0.3–0.4 mm plus 1–3 pairs of narrow, submarginal oil-glands). |
coherent (falling together), linear or linear-oblanceolate, 5–7 × 1–2 mm (dotted with scattered, oval oil-glands 0.2–0.3 mm). |
Heads | borne singly. |
borne singly or in condensed, cymiform arrays. |
Cypselae | 2.5–4.5 mm, strigillose (hairs tips acute or blunt); ray pappi of 1–2 awns 3–3.5 mm; disc pappi of 2–30 unequal bristles 3–5 mm. |
3–3.5 mm (pericarps darkening, not swelling, ovules abortive), strigillose to short-pilose; pappi of 2 (ray) or 5 (disc) slender, antrorsely scabrid, aristate scales 2–2.5 mm, sometimes with additional shorter scales or bristles. |
2n | = 24, 48. |
= 3x = 36. |
Pectis longipes |
Pectis ×floridana |
|
Phenology | Flowering Apr–Nov. | Flowering Sep–Dec. |
Habitat | Grasslands, oak-juniper-mesquite woodlands | Roadsides |
Elevation | 900–1700 m (3000–5600 ft) | 0–50 m (0–200 ft) |
Distribution |
AZ; NM; Mexico (Chihuahua, Durango, Sonora)
|
FL |
Discussion | Pectis longipes has been listed from Texas in floras; I have seen no collections from that state. Pectis longipes comprises two cytological races. Diploid, spicy-scented plants occur throughout the range. In southern Arizona, the diploid race is broadly sympatric but locally allopatric with a tetraploid, lemon-scented race. The tetraploid race is nested within the range of the diploids. The races are easily separable by odor, and although they are very similar morphologically, they can be separated also by statistically significant differences in floral dimensions and pollen size (M. A. Luckow 1983). Based upon those minute differences, the type collection is diploid. Because the races are so similar morphologically and because so many of the specimens of P. longipes in herbaria bear no indication of odor, I chose not to give the cytological races formal recognition. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Pectis ×floridana is a triploid hybrid between P. glaucescens (2n = 48) and P. prostrata (2n = 24). The hybrids have been observed where the parental taxa grow together in roadside habitats in southern Florida. At the type locality, the hybrids were nearly as common as the parentals. Meiosis in the hybrids is very irregular; resulting pollen grains are malformed and variable in size and apparently all sterile. No fruits have been observed. Regeneration of the hybrids from season to season apparently requires new hybridization events. The hybrids superficially resemble Pectis linearifolia from which they differ in having spicy-scented rather than lemon-scented herbage, longer peduncles, and strongly carinate phyllaries that cohere at the bases and fall together as a group. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 21, p. 226. | FNA vol. 21, p. 226. |
Parent taxa | Asteraceae > tribe Heliantheae > subtribe Pectidinae > Pectis | Asteraceae > tribe Heliantheae > subtribe Pectidinae > Pectis |
Sibling taxa | ||
Name authority | A. Gray: Smithsonian Contr. Knowl. 5(6): 69. (1853) | D. J. Keil: Sida 11: 389. (1986) |
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