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cushion foxtail cactus, foxtail cactus

biznaga-partida partida, nipple beehive cactus

Habit Plants unbranched (rarely to 30 branches), usually much more than 1/2 protruding above ground level, stiff and usually erect (rarely sprawling and basal parts becoming buried and mistaken for rhizomes), densely and uniformly clothed by spines. Plants profusely branched, ultimately forming low mats or hemispheric mounds to 100 cm diam., immature branches sometimes predominant, conspicuously tuberculate with projecting spines.
Roots

diffuse or short taproots also present, largest roots basally less than 1/5 of stem diam.

± succulent in largest, often massive and difficult to excavate.

Stems

cylindric, 5–27+ × 4.5–9 cm;

tubercles 10–14 × 6–10 mm, stiff;

areolar glands absent;

parenchyma not mucilaginous;

druses in pith and cortex relatively sparse, some giant, to 1 mm, lenticular;

pith 1/5–1/4 of lesser stem diam.;

medullary vascular system present (its vascular bundles numerous, small, and close together) or, in young plants, absent.

deep-seated, aerial portion conspicuous, hemispheric to short cylindric, shape sometimes obscured by profusion of immature branches, 5–23 × (1.5–)4–8(–13.5) cm;

tubercles unusually large, conspicuous, (10–)15–38(–45) × 6–15 mm, ± flaccid or flabby;

areolar glands seasonally conspicuous;

areolar grooves short, extending 1/2–3/4 distance from spines toward tubercle axils;

parenchyma mucilaginous;

pith narrow, ca. 1/10 of lesser stem diam.;

medullary vascular system absent.

Spines

30–51 per areole, heavily or lightly pigmented, tan to purplish gray or white proximally, black or sepia distally, darkest when fresh, weathering to blackish, radial spines slightly contrasting with centrals, dull creamy white, dark tips present, usually purplish black;

radial spines 18–33 per areole, 12–18 × 0.15–0.45 mm;

subcentral spines 1–3 often present;

outer central spines 6–15 per areole, always radiating in adults protruding at all angles;

inner central spines 0–10 per areole (3–7 per areole on subadult plants), all porrect or nearly so, straight, largest spines 10–23 × 0.5–0.9 mm.

7–21[–55] per areole;

radial spines (3–)9–15(–18) per areole, white, gray, tan, or brown, (9–)16–25(–50) mm;

subcentral spines 2–3 in adaxial part of areole;

central spines (1–)3–8 per areole, (tan to) pale gray to black, abaxial central spine porrect or descending, others weakly appressed or ± projecting spines, slightly curved, usually angular in cross section (terete), sometimes flat and grooved on 1 side and rounded on the other, often slightly flexible, (15–)25–35(–55) mm, all equal or abaxial spine longest.

Flowers

nearly apical, 20–30 × 25–39 mm;

outer tepals densely fringed;

inner tepals 21(–42) per flower, widely spreading, pale to intense rose-pink or rose-violet, with paler margins (white or pale rose), darker midstripes conspicuous, proximally white, 14–23 × 2–4 mm;

outer filaments white, pale rose, or pink with white bases, not greatly contrasting with inner tepals;

anthers bright dark yellow;

stigma lobes 5–9, widely spreading, pure white (rarely pale violet), 3–4 mm.

apical or nearly so, 30–50(–60) × (30–)40–70 mm;

outer tepals heavily fringed;

inner tepals 20–25 per flower, bright rose-pink or magenta, often with darker midstripes and paler margins, 30–40 × 4.5–6 mm;

outer filaments greenish white throughout or distally purplish pink;

anthers bright yellow;

stigma lobes 6–13, white or pale yellow, 3–6 mm.

Fruits

pale green throughout, narrowly fusiform-cylindric to narrowly obovoid, 16–25 × 6–12 mm, succulent;

floral remnant persistent Seeds reddish brown, obovoid to slightly comma-shaped, 1.3–1.6 mm, pitted.

dark green, ovoid to obpyriform or ellipsoid, (10–)13–25(–30) × 12–18 mm;

floral remnant strongly persistent.

Seeds

reddish brown, ± comma-shaped to spheric, 1.2–1.5 mm, finely and weakly raised-reticulate.

2n

= 22.

Coryphantha alversonii

Coryphantha macromeris

Phenology Flowering May–Jun; fruiting Jun–Jul. Flowering Feb–Sep; fruiting (May-)Aug–Dec.
Habitat Desert pavement or among stones, sandy or gravelly soils, alluvial fans, coarse alluvial deposits containing granite, gneiss, schist, and quartzite Chihuahuan desert scrub, Tamaulipan thorn scrub, nearly all substrates including nearly pure gypsum, gravelly soils, usually sandy alluvium or clay, rarely crevices or steep slopes
Elevation 70-600(-1200?) m (200-2000(-3900?) ft) 30-1700(-2000) m (100-5600(-6600) ft)
Distribution
from FNA
CA
[WildflowerSearch map]
from FNA
NM; TX; Mexico (Chihuahua, Coahuila, Durango, Zacatecas)
[WildflowerSearch map]
[BONAP county map]
Discussion

Of conservation concern.

Coryphantha alversonii is an allospecies in the C. vivipara species-group. Unlike other species in the subgenus Escobaria which have one layer, C. alversonii has two layers of hypodermis, probably reflecting its unusually xeric habitat. Coryphantha alversonii populations are localized, despite large areas of undisturbed desert at the proper altitude. Its disjunct distribution from the rest of the Coryphantha species, and its restriction to the relatively lush vegetation on alluvial fans in some areas, suggest a relictual taxon limited by drought, although this is the most strongly xerophytic species of Coryphantha.

The flowers, fruits, and seeds of Coryphantha alversonii are surprisingly small for such an otherwise robust species. The distinctive spine clusters of this species are strongly reminiscent of the Chihuahuan Desert species C. sneedii, only larger; the fruits and seeds of C. alversonii are intermediate in size and shape between those of C. sneedii and C. vivipara.

Although Coryphantha alversonii is expected on the Arizona side of the lower Colorado River, close to some of its known California populations, it remains undocumented from Arizona. Persistent reports of C. alversonii for Arizona (L. D. Benson 1969, 1982) are based on a misidentified fragment of either C. vivipara var. rosea or C. chlorantha, depending on its original tepal color.

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

Southern Texas populations of Coryphantha macromeris contain atypical individuals with proliferating small stems and shorter (stunted?) spines. Sexually mature stems branch from the tubercle axils, and the whole shoot becomes covered by immature branchlets. The immature branchlets proliferate profusely and asymmetrically faster than they can reach sexual maturity, obscuring the underlying symmetry of mature stems and forming irregular, asymmetric mounds. Such plants are the basis for C. macromeris var. runyonii (Britton & Rose) L. D. Benson, but they do not grow in pure populations. Therefore the name runyonii can not be used at varietal rank without including plants morphologically similar to typical C. macromeris from the Chihuahuan Desert.

Stunted or immature Coryphantha macromeris are variable, keying to Coryphantha with some difficulty, often having only 5–7 radial spines and lacking central spines. The strongly mucilaginous cortex is a useful field mark; even small slices of living tubercle tissue are visibly and tangibly slimy.

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

Source FNA vol. 4. FNA vol. 4, p. 224.
Parent taxa Cactaceae > subfam. Cactoideae > Coryphantha Cactaceae > subfam. Cactoideae > Coryphantha
Sibling taxa
C. chaffeyi, C. chlorantha, C. dasyacantha, C. duncanii, C. echinus, C. hesteri, C. macromeris, C. minima, C. missouriensis, C. nickelsiae, C. ramillosa, C. recurvata, C. robbinsorum, C. robertii, C. robustispina, C. sneedii, C. sulcata, C. tuberculosa, C. vivipara
C. alversonii, C. chaffeyi, C. chlorantha, C. dasyacantha, C. duncanii, C. echinus, C. hesteri, C. minima, C. missouriensis, C. nickelsiae, C. ramillosa, C. recurvata, C. robbinsorum, C. robertii, C. robustispina, C. sneedii, C. sulcata, C. tuberculosa, C. vivipara
Synonyms Cactus radiosus var. alversonii, C. vivipara Mammillaria macromeris, C. macromeris var. runyonii, C. macromeris, C. pirtlei, C. runyonii, Lepidocoryphantha macromeris
Name authority (J. M. Coulter) Orcutt: Cactography 1926(1): 3. (1926) (Engelmann) Lemaire: Cactées, 35. (1868)
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