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bonker hedgehog, pinkflower hedgehog cactus

Habit Plants 5–35-branched, ultimately forming clumps, branching at or before sexual maturation. Trees, shrubs, or short perennial plants, solitary to forming mats, columnlike or barrel-shaped to spheric stem succulents, sometimes geophytic or epiphytic, erect to prostrate, scrambling, climbing, or hanging, freely branched or unbranched.
Roots

diffuse, taproots, or tuberlike, sometimes adventitous.

Stems

mostly erect, ovoid to cylindric, 15–30(–50) × 3.5–7 cm;

ribs (11–)12–18(–20), crests slightly undulate;

areoles 8–20 mm apart.

segmented or unsegmented, usually conspicuously succulent with thick cortex and pith, surface usually ribbed or tuberculate, usually somewhat woody with wood confined to internal ring, bark sometimes becoming proximally hardened and woodlike;

areoles circular to linear [protracted into finger-shaped shoots in Neoraimondia of South America], hourglass-shaped in some genera, with spiny portion separated from flowering portion by a groove in the stem surface, spiny areoles completely separate from flowering areoles in some genera, bearing 0–90 spines, glochids absent.

Leaves

absent or rudimentary and microscopic or nearly so, less than 1 mm.

Spines

(9–)12–17 per areole, straight in short-spined forms, sometimes curved or twisted in long-spined forms, appressed (radial spines) or porrect to spreading or descending (central spines when present), dull yellowish to brown or white to gray, often brown to black especially at bases or tips;

radial spines (9–)11–16 per areole, 5–18 mm;

central spines (0–)1(–3) per areole, 2–100 mm, white to yellow or brown, often becoming gray, all terete.

acicular, subulate, daggerlike, ribbonlike, hairlike, or bristlelike, smooth, rough, striate, or annulate-ridged, glabrous (rarely pubescent), epidermis intact, not separating as sheath.

Flowers

5–7 × 4–9 cm;

flower tube 12–20 × 10–30 mm;

flower tube hairs 1 mm;

inner tepals deep magenta (to dark purple) with darker midstripes, proximally green (to very dark purple), 20–60 × 8.5–20 mm, tips relatively thin and delicate;

anthers yellow;

nectar chamber 2–4 mm.

diurnal to nocturnal, bisexual (rarely unisexual or functionally so), solitary in areoles (rarely several), radially symmetric (rarely bilateral), sessile, broadly salverform, urceolate, funnelform, or long tubular;

flower tube epigynous, usually conspicuous, adnate to upward extension of stem surrounding ovary, 0.2–15[–30] cm;

triangular leaflike bracts or small scales sometimes present on ovary and flower tube;

nectary often apparent, forming open chamber surrounding base of style.

Fruits

bright red or orange red, 15–25 mm, pulp white (or pale pink).

dehiscent or indehiscent, depressed-spheric or spheric to long clavate, juicy, fleshy, or dry;

perianth persistent or deciduous.

Seeds

1–3000+, yellowish, reddish, brown, or black, spheric, comma-shaped, lenticular-reniform, pyriform, or obovoid, 0.4–5 mm, rarely strophiolate, never arillate.

2n

= 22.

Echinocereus bonkerae

Cactaceae subfam. cactoideae

Phenology Flowering Mar–May; fruiting 2 months after flowering.
Habitat Sonoran Desert upland, interior chaparral, desert grasslands, pinyon-juniper woodlands
Elevation 700-2000 m (2300-6600 ft)
Distribution
from FNA
AZ
[WildflowerSearch map]
[BONAP county map]
Almost throughout New World from southern Canada to s South America; Rhipsalis disjunct to Africa; Madagascar; and Sri Lanka; some species in horticulture almost worldwide
Discussion

Plants in most populations of Echinocereus bonkerae have radial spines almost pectinately arranged and central spines very short or absent, creating the superficial appearance of E. dasyacanthus, E. pectinatus, or similar species. Formerly, all short-spined plants in central and southern Arizona were treated as E. bonkerae, including unusually short-spined individuals of E. fendleri and E. fasciculatus. Today we recognize that E. bonkerae, E. fendleri, and E. fasciculatus all vary from short-spined to long-spined.

Populations at the lowest altitude for the species have taller stems and unusually long, slender central spines (to 10 cm); they have recently been named Echinocereus apachensis. Such plants were part of the basis for L. D. Benson’s polyphyletic concept (1969, 1982) of E. fasciculatus var. boyce-thompsonii (see 8. E. fasciculatus).

Echinocereus bonkerae is a poorly defined species, frequently lumped with E. fendleri or E. fasciculatus, and it is not always identifiable in the field. Although rib number, blooming season, habitat preference, and, in particular regions, spine length or central spine presence are helpful characteristics, ploidy level is the most objective criterion for distinguishing E. bonkerae from E. fasciculatus. Immature plants of E. bonkerae are like E. fasciculatus and unlike the immature plants of E. fendleri, which are tuberculate with their spines long, few, soft, and often curved or twisted.

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

Genera ca. 111, species ca. 1500 (28 genera, 121 species in the flora).

Subfamily Cactoideae is the most diverse group of the Cactaceae, in terms of size, architecture, habitat, and habit. The vast majority of North American species are xerophytic, with columnar to spheric or barrel-shaped stems. A few are geophytic, that is, stems are mostly deep-seated in the soil substrate, often with the plant consisting mostly of an enlarged taproot and the visible parts of the stems appearing nearly flush with the soil surface or nearly buried during drought, becoming taller and slightly more conspicuous only during the growing season. Fewer species still, are epiphytic, and those only in the tropical and subtropical regions of North America and South America.

In the following treatments, most authors have attempted to recognize varieties wherever current evidence is compelling. Where evidence is equivocal, our tendency has been to include greater variability within varieties and, hence, fewer formal trinomials. Unfortunately, in the absence of strong supporting evidence, herbarium specimens of cacti are usually inadequate for the purpose of making taxonomic decisions. As a consequence, some populations of conservation interest here have been placed into synonmy before critical studies have been conducted to determine quantitatively and objectively how distinct each population is, or which deserve varietal status. Authors do not intend to imply that other varieties should not eventually be recognized. More systematic work, including DNA research and field research of all variants, is needed as a prelude to reassessing the status of currently listed and proposed populations. Such populations need to be protected during the entire phase of analysis and reassessment.

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

Source FNA vol. 4. FNA vol. 4. Author: Bruce D. Parfitt.
Parent taxa Cactaceae > subfam. Cactoideae > Echinocereus Cactaceae
Sibling taxa
E. arizonicus, E. berlandieri, E. chisosensis, E. coccineus, E. dasyacanthus, E. davisii, E. engelmannii, E. enneacanthus, E. fasciculatus, E. fendleri, E. ledingii, E. nicholii, E. papillosus, E. pectinatus, E. pentalophus, E. poselgeri, E. pseudopectinatus, E. reichenbachii, E. rigidissimus, E. stramineus, E. triglochidiatus, E. viridiflorus
Subordinate taxa
Synonyms E. apachensis, E. fasciculatus var. bonkerae, E. fendleri var. bonkerae
Name authority Thornber & Bonker: Fantast. Clan, 71, 85, plates opposite 23, 72. (1932) Eaton: Bot. Dict. ed. 4, 43. (1836)
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