Pectis |
Pectis longipes |
|||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chinchweed |
longstalk chinchweed, longstalk cinchweed, mat cinchweed |
|||||||||||||||||||||||||||||||||||||||||||||||||
Habit | Annuals or perennials, 1–120 cm (herbage often lemon or spicy scented). | Perennials, 8–25 cm (rhizomes branched, 1–10 mm diam.); herbage lemon-scented or spicy-scented. | ||||||||||||||||||||||||||||||||||||||||||||||||
Stems | prostrate to erect, simple to much branched. |
ascending to erect (very leafy), glabrous. |
||||||||||||||||||||||||||||||||||||||||||||||||
Leaves | cauline; opposite; usually sessile; blades mostly linear to elliptic, oblanceolate, oblong, or obovate, margins usually setose-ciliate (mostly near bases), faces glabrous or hairy (abaxial and/or margins dotted with oil-glands). |
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). |
||||||||||||||||||||||||||||||||||||||||||||||||
Peduncles | (30–)50–160 mm. |
|||||||||||||||||||||||||||||||||||||||||||||||||
Involucres | campanulate, cylindric, ellipsoid, or fusiform, 2–8+ mm diam. |
campanulate. |
||||||||||||||||||||||||||||||||||||||||||||||||
Receptacles | flat to hemispheric, smooth or pitted, epaleate. |
|||||||||||||||||||||||||||||||||||||||||||||||||
Ray florets | 3–15[–21], pistillate, fertile (inserted on phyllary bases); corollas yellow, often reddened abaxially (often drying white to purplish; laminae elliptic, entire or 2- or 3-lobed, glabrous or proximally glandular-puberulent). |
(8–)13(–15); corollas 8–12 mm. |
||||||||||||||||||||||||||||||||||||||||||||||||
Disc florets | [1–]3–55[–100], usually bisexual; corollas yellow (sometimes drying white to purplish), tubes shorter than narrowly funnelform throats, lobes (4–)5, deltate to lance-ovate (lobes ± equal and corollas actinomorphic, not 2-lipped, or lobes unequal with 3 or 4 forming an adaxial lip opposite 1-lobed lip and corollas zygomorphic, 2-lipped, all lobes glabrous or proximally glandular-puberulent; anther bases rounded or subcordate, apical appendages rounded or emarginate; styles included to long-exserted, branches ± papillose knobs). |
25–50; corollas 4–6 mm (2-lipped). |
||||||||||||||||||||||||||||||||||||||||||||||||
Phyllaries | 3–15[–21] in 1 series (usually distinct, falling individually, each with a ray cypsela, sometimes cohering at bases, falling together as units enclosing all cypselae of a head; individually convex, indurate-keeled, narrowly to broadly hyaline-margined, apices often ciliolate, bearing oil-glands on margins and/or faces). |
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). |
||||||||||||||||||||||||||||||||||||||||||||||||
Calyculi | 0. |
|||||||||||||||||||||||||||||||||||||||||||||||||
Heads | radiate, borne singly or in congested to open, cymiform arrays (peduncles usually bracteate). |
borne singly. |
||||||||||||||||||||||||||||||||||||||||||||||||
Cypselae | (blackish or dark brown) cylindric to narrowly clavate, ribbed or angled, puberulent to pilose; pappi persistent, usually of awns, bristles, or scales, sometimes coroniform. |
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. |
||||||||||||||||||||||||||||||||||||||||||||||||
x | = 12. |
|||||||||||||||||||||||||||||||||||||||||||||||||
2n | = 24, 48. |
|||||||||||||||||||||||||||||||||||||||||||||||||
Pectis |
Pectis longipes |
|||||||||||||||||||||||||||||||||||||||||||||||||
Phenology | Flowering Apr–Nov. | |||||||||||||||||||||||||||||||||||||||||||||||||
Habitat | Grasslands, oak-juniper-mesquite woodlands | |||||||||||||||||||||||||||||||||||||||||||||||||
Elevation | 900–1700 m (3000–5600 ft) | |||||||||||||||||||||||||||||||||||||||||||||||||
Distribution |
North America; Mexico; Central America; South America; West Indies; Pacific Islands (Galapagos Islands, Hawaii) |
AZ; NM; Mexico (Chihuahua, Durango, Sonora)
|
||||||||||||||||||||||||||||||||||||||||||||||||
Discussion | Species about 90 (13, including 1 hybrid, in the flora). Pectis is unusual among Compositae in having the C4 photosynthetic pathway and the accompanying Kranz anatomy—leaves with vascular bundle sheath cells that contain numerous chloroplasts (B. N. Smith and B. L. Turner 1975). All of the closely related genera have the C3 pathway. The selective advantage imparted by C4 photosynthesis (greatly reduced photorespiration in bundle sheath cells) has enabled Pectis species to occupy a variety of hot, dry habitats including deserts, tropical and subtropical grasslands, arid scrublands, and tropical beaches. Some species of Pectis grow in hot desert areas of the western United States following summer precipitation. Leaves and phyllaries in all Pectis species are dotted with embedded pellucid glands (here called oil-glands). In some species, the liquid within the schizogenous cavities includes a mixture of strongly scented monoterpenes; in other species the gland contents have little or no aroma. Herbage containing strongly scented essential oils are described as “lemon-scented” when citral is the predominant compound and “spicy-scented” when other oils are predominant. For most taxa the odor (or lack thereof) of the crushed herbage is a readily apparent field characteristic. Unfortunately, labels of most herbarium specimens lack information on odor. Intact glands on herbarium specimens may retain liquid contents for years; odors may change as the specimens age. On living specimens, the glands are translucent; on herbarium specimens, they tend to be golden brown or blackish. The glands probably function as a deterrent to herbivores, including insects. Ray florets of Pectis are inserted directly onto the bases of the phyllaries, and the phyllaries and ray cypselae tend to fall together when the heads shatter at maturity. The numbers of phyllaries and ray florets per Pectis capitulum vary along the Fibonacci series and rarely deviate from the sequence (i.e., in Pectis, the modal numbers of phyllaries and rays are 3, 5, 8, 13, and 21). Pectis coulteri Harvey & A. Gray has been attributed in floras to California and Arizona on the basis of the ambiguously labeled type collection (“California,” without locality or date, T. Coulter 331, holotype TCD) and speculations as to its origin. This species is known to occur only from central Sonora to northern Sinaloa, Mexico, and has never been documented in the United States. The type was probably collected in Sonora (D. J. Keil 1975). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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.) |
||||||||||||||||||||||||||||||||||||||||||||||||
Key |
|
|||||||||||||||||||||||||||||||||||||||||||||||||
Source | FNA vol. 21, p. 222. | FNA vol. 21, p. 226. | ||||||||||||||||||||||||||||||||||||||||||||||||
Parent taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||
Sibling taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||
Subordinate taxa | ||||||||||||||||||||||||||||||||||||||||||||||||||
Name authority | Linnaeus: Syst. Nat. ed. 10, 2: 1221. (1759) | A. Gray: Smithsonian Contr. Knowl. 5(6): 69. (1853) | ||||||||||||||||||||||||||||||||||||||||||||||||
Web links |