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branch pencil cholla, diamond cholla, pencil cactus

Habit Trees or shrubs, intricately branched, 0.5–2 m. Stem segments firmly attached, green drying gray and ropelike, cylindric, 2–8(–10) × 0.4–1 cm; tubercles rhombic, convex (flattened upon drying), 0.4–0.8 cm; areoles subcircular abaxially, adaxially becoming usually deltate-linear; glochid-bearing portion protruding distally, wedged between bases of 2 adjacent tubercles, (3–)4–7 × 1–1.5(–2) mm; wool tan to white. Trees or shrubs, sometimes forming clumps or mats, sometimes geophytes, trailing to erect.
Roots

diffuse or tuberlike.

Stems

segmented throughout or only in ultimate branches, succulent (less noticeably so in some Cylindropuntia), often woody, especially toward base, smooth or tuberculate;

areoles cushionlike, circular or nearly so (to linear), usually bearing conspicuous spines and always bearing glochids.

Leaves

of brief duration, promptly deciduous, present only during initial growth of stem segments and flowers [persistent], conic or somewhat flattened, succulent.

Spines

0–5 per areole, usually in distal areoles or sometimes absent or nearly so, tan to red-brown to deep purple, aging gray;

major abaxial spines 0–1(–2), the longest spine spreading, (1.5–)2.5–6 cm;

adaxial spines usually reflexed, short to ± 1 cm;

sheaths baggy.

slender to stout (to hairlike), terete to strongly flattened, usually smooth, sometimes barbed or roughened, epidermis intact or partly to wholly separating from body of spine as sheath that hangs onto spine.

Glochids

in subcircular to linear adaxial tuft, yellow to tan to brown, to 2 mm.

Flowers

inner tepals bronze-red ± suffused rose, with mid stripes darker, ovate, 6–13 mm, acute-apiculate to attenuate;

filaments greenish;

anthers yellow;

style whitish or blushed with rose-pink or light green;

stigma lobes whitish.

diurnal (opening late afternoon or night in Cylindropuntia fulgida), bisexual (sometimes functionally staminate or pistillate), solitary in areoles [terminal], radially or bilaterally symmetric (flower curved and/or the ovary flattened), sessile, rotate, cup-shaped, or salverform;

flower tube epigynous, short adnate to extension of stem segment surrounding ovary;

nectary at base of style, open or sometimes covered by outgrowths of proximal portion of style base or of flower tube wall as specialized nectar chamber.

Fruits

maturing tan, ellipsoid to stipitate-ellipsoid, 15–30 × 10–15 mm, dry at maturity, tuberculate, developing increasingly burlike, with many bristlelike spines;

areoles (32–)40–66, evenly spaced, woolly.

indehiscent, cylindric, ellipsoid, ovoid, or subspheric, sometimes clavate, fleshy, juicy (bleeding), or quickly drying;

perianth and contained flower parts shriveling and abscising basally as single unit including floral cup, leaving deep to almost flat scar (umbilicus) atop fruit.

Seeds

pale yellow to tan-gray, angular to squarish in outline, warped, 4–4.5 × 3.5–4 mm, sides irregularly concave-convex;

girdle smooth.

0 (sterile) or 1–400+, yellowish, tan, gray, or brown, flattened to subspheric, 2–7 mm, each completely enclosed by bony funicular envelope, glabrous or sometimes pubescent, its vascular bundle forming girdle around seed, sometimes enlarged and protruding as ridge or wing.

2n

= 22, 44.

Cylindropuntia ramosissima

Cactaceae subfam. opuntioideae

Phenology Flowering spring–summer (Apr–Aug).
Habitat Mojave and Sonoran deserts, washes, flats, and bajadas, sandy loam, desert pavement, stony volcanic substrates
Elevation 50-1100 m (200-3600 ft)
Distribution
from FNA
AZ; CA; NV; Mexico (Baja California, Sonora)
[WildflowerSearch map]
[BONAP county map]
Throughout New World from near Arctic Circle to Patagonia [Introduced especially in tropical, subtropical, and warm-temperate regions almost worldwide]
Discussion

Genera 16, species ca. 350 (5 genera, 66 species in the flora).

All genera of Opuntioideae in the flora have been combined into the genus Opuntia at various times. Recent research findings in morphology, anatomy, palynology, seed characteristics, host-herbivore relations, and chloroplast and nuclear DNA make untenable the maintenance of the single genus Opuntia. Unlike some genera of subfam. Cactoideae, the segregate genera of Opuntioideae are not known to produce intergeneric hybrids.

Identification of the species within subfam. Opuntioideae is difficult, in part because of widespread phenotypic plasticity, interspecific hybridization, polyploidy, and apomixis (clonal seeds and stems), which play important evolutionary roles, particularly in Cylindropuntia and Opuntia. Habit descriptions, color photographs (including close-ups), and meiotic chromosome counts are very helpful in identification of species. Also, good herbarium specimens require at least two or three consecutive stem segments, flowers and/or fruits, and detailed notes on all fresh flower parts and fruits as to color (particularly inner tepals, filaments, fresh stigma lobes, and fruits), shape, and size (because of extensive shrinkage on drying). Spine characters are generally based on well-developed areoles, mostly in distal portions of stem segments. Yellow spines usually turn dark red to black with age, including those on herbarium sheets.

(Discussion copyrighted by Flora of North America; reprinted with permission.)

Source FNA vol. 4, p. 118. FNA vol. 4, p. 102. Author: Donald J. Pinkava.
Parent taxa Cactaceae > subfam. Opuntioideae > Cylindropuntia Cactaceae
Sibling taxa
C. abyssi, C. acanthocarpa, C. arbuscula, C. bigelovii, C. californica, C. davisii, C. echinocarpa, C. fulgida, C. ganderi, C. imbricata, C. kleiniae, C. leptocaulis, C. munzii, C. prolifera, C. spinosior, C. tunicata, C. versicolor, C. whipplei, C. wolfii, C. ×kelvinensis, C. ×tetracantha
Subordinate taxa
Synonyms Opuntia ramosissima, Opuntia tessellata
Name authority (Engelmann) F. M. Knuth: in C. Backeberg and F. M. Knuth, Kaktu s-ABC, 122. (1935) Burnett: Outlines Bot. 2: 742, 1130. (1835)
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