Difference between revisions of "Coryphantha"
Cactées, 32. 1868.
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|common_names=Pincushion cactus | |common_names=Pincushion cactus | ||
− | |basionyms={{Treatment/ID/ | + | |basionyms={{Treatment/ID/Basionym |
|name=Mammillaria subg. Coryphantha | |name=Mammillaria subg. Coryphantha | ||
|authority=Engelmann | |authority=Engelmann | ||
+ | |rank=subgenus | ||
+ | |publication_title=Proc. Amer. Acad. Arts | ||
+ | |publication_place=3: 264. 1856 (as Mamillaria) | ||
}} | }} | ||
|synonyms={{Treatment/ID/Synonym | |synonyms={{Treatment/ID/Synonym | ||
|name=Aulacothelae | |name=Aulacothelae | ||
|authority=Lemaire | |authority=Lemaire | ||
− | }}{{Treatment/ID/Synonym | + | |rank=genus |
+ | }} {{Treatment/ID/Synonym | ||
|name=Cochiseia | |name=Cochiseia | ||
|authority=W. Earle | |authority=W. Earle | ||
− | }}{{Treatment/ID/Synonym | + | |rank=genus |
+ | }} {{Treatment/ID/Synonym | ||
|name=Cumarinia | |name=Cumarinia | ||
|authority=Buxbaum | |authority=Buxbaum | ||
− | }}{{Treatment/ID/Synonym | + | |rank=genus |
+ | }} {{Treatment/ID/Synonym | ||
|name=Escobaria | |name=Escobaria | ||
|authority=Britton & Rose | |authority=Britton & Rose | ||
− | }}{{Treatment/ID/Synonym | + | |rank=genus |
+ | }} {{Treatment/ID/Synonym | ||
|name=Escobesseya | |name=Escobesseya | ||
|authority=Hester | |authority=Hester | ||
− | }}{{Treatment/ID/Synonym | + | |rank=genus |
+ | }} {{Treatment/ID/Synonym | ||
|name=Lepidocoryphantha | |name=Lepidocoryphantha | ||
|authority=Backeberg | |authority=Backeberg | ||
− | }}{{Treatment/ID/Synonym | + | |rank=genus |
+ | }} {{Treatment/ID/Synonym | ||
|name=Neobesseya | |name=Neobesseya | ||
|authority=Britton & Rose | |authority=Britton & Rose | ||
+ | |rank=genus | ||
}} | }} | ||
|hierarchy=Cactaceae;Cactaceae subfam. Cactoideae;Coryphantha | |hierarchy=Cactaceae;Cactaceae subfam. Cactoideae;Coryphantha | ||
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− | --><span class="statement" id="st-undefined" data-properties=""><b>Plants </b>erect, spheric and unbranched or, if branched, then ultimately forming low clumps or small mats. <b>Roots</b> diffuse, succulent taproots (sometimes tuberlike or massive), or in some species ultimately adventitious from bases of branches. <b>Stems</b> unsegmented, hemispheric, spheric, ovoid, or cylindric, sometimes flat-topped, tuberculate, 1–20(–50) × 1–15 cm after sexual maturity; tubercles conic to hemispheric or cylindric, never coalescing into ribs, protruding conspicuously, grooved on their adaxial (upper) sides in sexually mature plants, i.e., areoles of sexually mature plants each consisting of fertile meristem (often woolly) in tubercle axil and spine cluster on tubercle apex, the two connected by a linear isthmus (areolar extension, often short woolly) recessed into an areolar groove on adaxial side of tubercle (groove extends only 1/2–3/4 distance from spine cluster to tubercle axil in C. macromeris); areolar glands present or absent; cortex and pith usually mucilaginous or with mucilage confined to flowers and fruits. <b>Spines</b> 3–95 per areole, color various, needlelike (peglike in C. minima), usually differentiated into radial and central spines; radial spines straight or curved; central spines, when present, straight or curved (hooked in C. robustispina), terete, 4–55 mm. <b>Flowers</b> diurnal (sometimes ± vespertine in C. tuberculosa), borne at or near stem apex (lateral in C. recurvata), on new growth of current year and/or last-produced areoles of preceding year (fruiting zone in some species becoming displaced outward and downward by apical vegetative growth after flowering), campanulate or funnelform to nearly salverform with recurved tepals, 1–6.5 × 0.6–10 cm; outer tepals entire or fringed; inner tepals variously colored, never pure red or blue, 4.5–40 × 1–15 mm, often glossy, margins entire, toothed, fringed, or erose; scales on ovary none or few, narrow or rudimentary, entire or erose, axils naked, spineless; stigma lobes 4–13, white to yellow or orange-yellow (rarely pinkish), 0.5–8 mm. <b>Fruits</b> indehiscent, green or red, spheric, ellipsoid, ovoid to narrowly fusiform, or obovoid, 1.5–50 × 1.5–20 mm, usually juicy, sometimes slimy or fleshy (dry in C. minima), scales usually absent (or few), spines absent; pulp colorless to white, greenish, or pinkish; floral remnant persistent or deciduous. <b>Seeds</b> usually reddish brown or black, sometimes yellowish, reniform, comma-shaped, obovoid, or spheric, 0.8–3.5 mm in greatest diam., shiny or glossy; testa smooth, raised-reticulate, or pitted; strophiole (unsclerified tissue in/around hilum) small or large, flat or slightly protruding, never surrounding micropyle, replaced by a narrow raphe in some species (e.g., C. ramillosa); sclerified collar between hilum and micropyle short, solid or grooved, nearly open in some species. <b>x</b> = 11.</span><!-- | + | --><span class="statement" id="st-undefined" data-properties=""><b>Plants </b>erect, spheric and unbranched or, if branched, then ultimately forming low clumps or small mats. <b>Roots</b> diffuse, succulent taproots (sometimes tuberlike or massive), or in some species ultimately adventitious from bases of branches. <b>Stems</b> unsegmented, hemispheric, spheric, ovoid, or cylindric, sometimes flat-topped, tuberculate, 1–20(–50) × 1–15 cm after sexual maturity; tubercles conic to hemispheric or cylindric, never coalescing into ribs, protruding conspicuously, grooved on their adaxial (upper) sides in sexually mature plants, i.e., areoles of sexually mature plants each consisting of fertile meristem (often woolly) in tubercle axil and spine cluster on tubercle apex, the two connected by a linear isthmus (areolar extension, often short woolly) recessed into an areolar groove on adaxial side of tubercle (groove extends only 1/2–3/4 distance from spine cluster to tubercle axil in <i>C. macromeris</i>); areolar glands present or absent; cortex and pith usually mucilaginous or with mucilage confined to flowers and fruits. <b>Spines</b> 3–95 per areole, color various, needlelike (peglike in <i>C. minima</i>), usually differentiated into radial and central spines; radial spines straight or curved; central spines, when present, straight or curved (hooked in <i>C. robustispina</i>), terete, 4–55 mm. <b>Flowers</b> diurnal (sometimes ± vespertine in <i>C. tuberculosa</i>), borne at or near stem apex (lateral in <i>C. recurvata</i>), on new growth of current year and/or last-produced areoles of preceding year (fruiting zone in some species becoming displaced outward and downward by apical vegetative growth after flowering), campanulate or funnelform to nearly salverform with recurved tepals, 1–6.5 × 0.6–10 cm; outer tepals entire or fringed; inner tepals variously colored, never pure red or blue, 4.5–40 × 1–15 mm, often glossy, margins entire, toothed, fringed, or erose; scales on ovary none or few, narrow or rudimentary, entire or erose, axils naked, spineless; stigma lobes 4–13, white to yellow or orange-yellow (rarely pinkish), 0.5–8 mm. <b>Fruits</b> indehiscent, green or red, spheric, ellipsoid, ovoid to narrowly fusiform, or obovoid, 1.5–50 × 1.5–20 mm, usually juicy, sometimes slimy or fleshy (dry in <i>C. minima</i>), scales usually absent (or few), spines absent; pulp colorless to white, greenish, or pinkish; floral remnant persistent or deciduous. <b>Seeds</b> usually reddish brown or black, sometimes yellowish, reniform, comma-shaped, obovoid, or spheric, 0.8–3.5 mm in greatest diam., shiny or glossy; testa smooth, raised-reticulate, or pitted; strophiole (unsclerified tissue in/around hilum) small or large, flat or slightly protruding, never surrounding micropyle, replaced by a narrow raphe in some species (e.g., <i>C. ramillosa</i>); sclerified collar between hilum and micropyle short, solid or grooved, nearly open in some species. <b>x</b> = 11.</span><!-- |
-->{{Treatment/Body | -->{{Treatment/Body | ||
|distribution=w North America;Mexico;West Indies (Cuba). | |distribution=w North America;Mexico;West Indies (Cuba). | ||
|discussion=<p>Species 60–70 (20 in the flora).</p><!-- | |discussion=<p>Species 60–70 (20 in the flora).</p><!-- | ||
− | --><p>Coryphantha may be polyphyletic, or paraphyletic, with respect to Mammillaria, from which it differs primarily by the presence of an adaxial areolar groove on tubercles of sexually mature coryphanthas. Most species of Coryphantha produce a more or less apical tuft of flowers from the current growth; most mammillarias bloom in a ring from older areoles at least 1 cm from the stem apex. Coryphantha recurvata is an exception with a ring of flowers as in most species of Mammillaria. Some species in each genus display intermediate floral positions. In both genera, pitted seeds characterize putatively primitive species.</p><!-- | + | --><p><i>Coryphantha</i> may be polyphyletic, or paraphyletic, with respect to <i>Mammillaria</i>, from which it differs primarily by the presence of an adaxial areolar groove on tubercles of sexually mature coryphanthas. Most species of <i>Coryphantha</i> produce a more or less apical tuft of flowers from the current growth; most mammillarias bloom in a ring from older areoles at least 1 cm from the stem apex. <i>Coryphantha recurvata</i> is an exception with a ring of flowers as in most species of <i>Mammillaria</i>. Some species in each genus display intermediate floral positions. In both genera, pitted seeds characterize putatively primitive species.</p><!-- |
− | --><p>The coryphanthas with pitted seeds often are segregated as Escobaria (species numbered 8–20 here). That segregate, recognized by the International Cactaceae Systematics Group (ICSG) but not here, lacks the glands found in the areoles of typical Coryphantha. Such glands are ephemeral. The glands, occuring singly or in small groups usually at either end of each areolar groove, are spheroid or mushroom-shaped (then deeply nestled among short trichomes so appear to be hemispheric), smooth, colorful (red, green, purplish, orange, or yellow), and about 1 mm in diameter. Fallen glands leave circular gray scars.</p><!-- | + | --><p>The coryphanthas with pitted seeds often are segregated as Escobaria (species numbered 8–20 here). That segregate, recognized by the International <i>Cactaceae</i> Systematics Group (ICSG) but not here, lacks the glands found in the areoles of typical <i>Coryphantha</i>. Such glands are ephemeral. The glands, occuring singly or in small groups usually at either end of each areolar groove, are spheroid or mushroom-shaped (then deeply nestled among short trichomes so appear to be hemispheric), smooth, colorful (red, green, purplish, orange, or yellow), and about 1 mm in diameter. Fallen glands leave circular gray scars.</p><!-- |
− | --><p>Several species of Coryphantha closely resemble, and may be confused with, Neolloydia conoidea. Both genera have naked ovaries and grooved tubercles; however, Neolloydia has seeds like those of Ariocarpus or Lophophora. The tiny fruits of N. conoidea usually are overlooked, often leading to misidentifications. In immature plants of several genera that tend to be “ribbed” (e.g., Echinomastus), and in the adults of neotenous species, stems are tuberculate; however, the areolar extensions in those plants are shorter and/or wider than those of Coryphantha, and the tubercles usually are basally confluent, unlike the (linear) grooves and distinct tubercles of Coryphantha and Neolloydia.</p><!-- | + | --><p>Several species of <i>Coryphantha</i> closely resemble, and may be confused with, <i>Neolloydia conoidea</i>. Both genera have naked ovaries and grooved tubercles; however, <i>Neolloydia</i> has seeds like those of <i>Ariocarpus</i> or <i>Lophophora</i>. The tiny fruits of <i>N. conoidea</i> usually are overlooked, often leading to misidentifications. In immature plants of several genera that tend to be “ribbed” (e.g., <i>Echinomastus</i>), and in the adults of neotenous species, stems are tuberculate; however, the areolar extensions in those plants are shorter and/or wider than those of <i>Coryphantha</i>, and the tubercles usually are basally confluent, unlike the (linear) grooves and distinct tubercles of <i>Coryphantha</i> and <i>Neolloydia</i>.</p><!-- |
--><p>As many as fourteen species of coryphanthas may occur sympatrically, with no natural hybrids dectected. Flowers may be few and ephemeral; however, identifications based on vegetative traits may be difficult because of polymorphism and age-related heteromorphic growth within populations, geographic variation within species, and parallel evolution among ecological counterparts in relatively distant lineages.</p><!-- | --><p>As many as fourteen species of coryphanthas may occur sympatrically, with no natural hybrids dectected. Flowers may be few and ephemeral; however, identifications based on vegetative traits may be difficult because of polymorphism and age-related heteromorphic growth within populations, geographic variation within species, and parallel evolution among ecological counterparts in relatively distant lineages.</p><!-- | ||
− | --><p>Calcium oxatate crystal aggregates (druses) in the stem parenchyma of Coryphantha are spheric, oblong, or lens-shaped masses like grains of sand. Most druses are only 0.1–0.4 mm diam., seen best with a compound microscope and polarizing filters, but five species (species 16–20) have unusually large druses (0.5–1 mm diam.) conspicuous to the naked eye. With practice, the thick pale-looking skin associated with a several-layered and/or druse-containing stem can be recognized.</p><!-- | + | --><p>Calcium oxatate crystal aggregates (druses) in the stem parenchyma of <i>Coryphantha</i> are spheric, oblong, or lens-shaped masses like grains of sand. Most druses are only 0.1–0.4 mm diam., seen best with a compound microscope and polarizing filters, but five species (species 16–20) have unusually large druses (0.5–1 mm diam.) conspicuous to the naked eye. With practice, the thick pale-looking skin associated with a several-layered and/or druse-containing stem can be recognized.</p><!-- |
--><p>Species with specialized mucilage cells in the pith and cortex of stems are wet with tangibly and visibly viscous slime when cut open. Mucilage usually can be seen and felt in healthy living tubercles. Fresh sections feel watery or mealy in species lacking specialized mucilage cells.</p><!-- | --><p>Species with specialized mucilage cells in the pith and cortex of stems are wet with tangibly and visibly viscous slime when cut open. Mucilage usually can be seen and felt in healthy living tubercles. Fresh sections feel watery or mealy in species lacking specialized mucilage cells.</p><!-- | ||
--><p>A medullary vascular system (when present) is a diffuse network of fine threadlike strands of wood inside the pith at the center of the stem, within the woody vascular cylinder. Such whitish vascular strands are seen by holding a light source behind a translucently thin stem section.</p><!-- | --><p>A medullary vascular system (when present) is a diffuse network of fine threadlike strands of wood inside the pith at the center of the stem, within the woody vascular cylinder. Such whitish vascular strands are seen by holding a light source behind a translucently thin stem section.</p><!-- | ||
--><p>Stem diameter includes the tubercles, unless otherwise stated; lesser stem diameter excludes the tubercles and is used only to define the relative size of the pith. Tubercle diameter is the maximum measurement of the cross section at midpoint between the base and apex of a tubercle. Spine thickness is measured midspine.</p><!-- | --><p>Stem diameter includes the tubercles, unless otherwise stated; lesser stem diameter excludes the tubercles and is used only to define the relative size of the pith. Tubercle diameter is the maximum measurement of the cross section at midpoint between the base and apex of a tubercle. Spine thickness is measured midspine.</p><!-- | ||
− | --><p>Flower length may be misinterpreted on flowers deeply hidden in the axils of the subtending tubercles. Accurate measurements of diameter require fully opened flowers (in some species the flower may not be fully open if the angle between the inner tepals and floral tube is less than 45º). Fruits with fully formed seeds may not be mature with respect to taxonomically important characters of fruit size and color. Ripe fruits are those that abscise easily from the plant with a gentle tug (although fruits of Coryphantha robustispina sometimes require a hard pull). A pitted seed testa is easily viewed with a hand lens. A weakly raised-reticulate seed testa is distinguishable from a smooth testa only with a lens (10× or greater magnification). A reticulate color pattern alone does not imply that the anticlinal cell walls actually protrude.</p> | + | --><p>Flower length may be misinterpreted on flowers deeply hidden in the axils of the subtending tubercles. Accurate measurements of diameter require fully opened flowers (in some species the flower may not be fully open if the angle between the inner tepals and floral tube is less than 45º). Fruits with fully formed seeds may not be mature with respect to taxonomically important characters of fruit size and color. Ripe fruits are those that abscise easily from the plant with a gentle tug (although fruits of <i>Coryphantha robustispina</i> sometimes require a hard pull). A pitted seed testa is easily viewed with a hand lens. A weakly raised-reticulate seed testa is distinguishable from a smooth testa only with a lens (10× or greater magnification). A reticulate color pattern alone does not imply that the anticlinal cell walls actually protrude.</p> |
|tables= | |tables= | ||
|references={{Treatment/Reference | |references={{Treatment/Reference | ||
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|publication year=1868 | |publication year=1868 | ||
|special status= | |special status= | ||
− | |source xml=https:// | + | |source xml=https://bitbucket.org/aafc-mbb/fna-data-curation/src/2e0870ddd59836b60bcf96646a41e87ea5a5943a/coarse_grained_fna_xml/V4/V4_411.xml |
|subfamily=Cactaceae subfam. Cactoideae | |subfamily=Cactaceae subfam. Cactoideae | ||
|genus=Coryphantha | |genus=Coryphantha |
Latest revision as of 21:58, 5 November 2020
Plants erect, spheric and unbranched or, if branched, then ultimately forming low clumps or small mats. Roots diffuse, succulent taproots (sometimes tuberlike or massive), or in some species ultimately adventitious from bases of branches. Stems unsegmented, hemispheric, spheric, ovoid, or cylindric, sometimes flat-topped, tuberculate, 1–20(–50) × 1–15 cm after sexual maturity; tubercles conic to hemispheric or cylindric, never coalescing into ribs, protruding conspicuously, grooved on their adaxial (upper) sides in sexually mature plants, i.e., areoles of sexually mature plants each consisting of fertile meristem (often woolly) in tubercle axil and spine cluster on tubercle apex, the two connected by a linear isthmus (areolar extension, often short woolly) recessed into an areolar groove on adaxial side of tubercle (groove extends only 1/2–3/4 distance from spine cluster to tubercle axil in C. macromeris); areolar glands present or absent; cortex and pith usually mucilaginous or with mucilage confined to flowers and fruits. Spines 3–95 per areole, color various, needlelike (peglike in C. minima), usually differentiated into radial and central spines; radial spines straight or curved; central spines, when present, straight or curved (hooked in C. robustispina), terete, 4–55 mm. Flowers diurnal (sometimes ± vespertine in C. tuberculosa), borne at or near stem apex (lateral in C. recurvata), on new growth of current year and/or last-produced areoles of preceding year (fruiting zone in some species becoming displaced outward and downward by apical vegetative growth after flowering), campanulate or funnelform to nearly salverform with recurved tepals, 1–6.5 × 0.6–10 cm; outer tepals entire or fringed; inner tepals variously colored, never pure red or blue, 4.5–40 × 1–15 mm, often glossy, margins entire, toothed, fringed, or erose; scales on ovary none or few, narrow or rudimentary, entire or erose, axils naked, spineless; stigma lobes 4–13, white to yellow or orange-yellow (rarely pinkish), 0.5–8 mm. Fruits indehiscent, green or red, spheric, ellipsoid, ovoid to narrowly fusiform, or obovoid, 1.5–50 × 1.5–20 mm, usually juicy, sometimes slimy or fleshy (dry in C. minima), scales usually absent (or few), spines absent; pulp colorless to white, greenish, or pinkish; floral remnant persistent or deciduous. Seeds usually reddish brown or black, sometimes yellowish, reniform, comma-shaped, obovoid, or spheric, 0.8–3.5 mm in greatest diam., shiny or glossy; testa smooth, raised-reticulate, or pitted; strophiole (unsclerified tissue in/around hilum) small or large, flat or slightly protruding, never surrounding micropyle, replaced by a narrow raphe in some species (e.g., C. ramillosa); sclerified collar between hilum and micropyle short, solid or grooved, nearly open in some species. x = 11.
Distribution
w North America, Mexico, West Indies (Cuba).
Discussion
Species 60–70 (20 in the flora).
Coryphantha may be polyphyletic, or paraphyletic, with respect to Mammillaria, from which it differs primarily by the presence of an adaxial areolar groove on tubercles of sexually mature coryphanthas. Most species of Coryphantha produce a more or less apical tuft of flowers from the current growth; most mammillarias bloom in a ring from older areoles at least 1 cm from the stem apex. Coryphantha recurvata is an exception with a ring of flowers as in most species of Mammillaria. Some species in each genus display intermediate floral positions. In both genera, pitted seeds characterize putatively primitive species.
The coryphanthas with pitted seeds often are segregated as Escobaria (species numbered 8–20 here). That segregate, recognized by the International Cactaceae Systematics Group (ICSG) but not here, lacks the glands found in the areoles of typical Coryphantha. Such glands are ephemeral. The glands, occuring singly or in small groups usually at either end of each areolar groove, are spheroid or mushroom-shaped (then deeply nestled among short trichomes so appear to be hemispheric), smooth, colorful (red, green, purplish, orange, or yellow), and about 1 mm in diameter. Fallen glands leave circular gray scars.
Several species of Coryphantha closely resemble, and may be confused with, Neolloydia conoidea. Both genera have naked ovaries and grooved tubercles; however, Neolloydia has seeds like those of Ariocarpus or Lophophora. The tiny fruits of N. conoidea usually are overlooked, often leading to misidentifications. In immature plants of several genera that tend to be “ribbed” (e.g., Echinomastus), and in the adults of neotenous species, stems are tuberculate; however, the areolar extensions in those plants are shorter and/or wider than those of Coryphantha, and the tubercles usually are basally confluent, unlike the (linear) grooves and distinct tubercles of Coryphantha and Neolloydia.
As many as fourteen species of coryphanthas may occur sympatrically, with no natural hybrids dectected. Flowers may be few and ephemeral; however, identifications based on vegetative traits may be difficult because of polymorphism and age-related heteromorphic growth within populations, geographic variation within species, and parallel evolution among ecological counterparts in relatively distant lineages.
Calcium oxatate crystal aggregates (druses) in the stem parenchyma of Coryphantha are spheric, oblong, or lens-shaped masses like grains of sand. Most druses are only 0.1–0.4 mm diam., seen best with a compound microscope and polarizing filters, but five species (species 16–20) have unusually large druses (0.5–1 mm diam.) conspicuous to the naked eye. With practice, the thick pale-looking skin associated with a several-layered and/or druse-containing stem can be recognized.
Species with specialized mucilage cells in the pith and cortex of stems are wet with tangibly and visibly viscous slime when cut open. Mucilage usually can be seen and felt in healthy living tubercles. Fresh sections feel watery or mealy in species lacking specialized mucilage cells.
A medullary vascular system (when present) is a diffuse network of fine threadlike strands of wood inside the pith at the center of the stem, within the woody vascular cylinder. Such whitish vascular strands are seen by holding a light source behind a translucently thin stem section.
Stem diameter includes the tubercles, unless otherwise stated; lesser stem diameter excludes the tubercles and is used only to define the relative size of the pith. Tubercle diameter is the maximum measurement of the cross section at midpoint between the base and apex of a tubercle. Spine thickness is measured midspine.
Flower length may be misinterpreted on flowers deeply hidden in the axils of the subtending tubercles. Accurate measurements of diameter require fully opened flowers (in some species the flower may not be fully open if the angle between the inner tepals and floral tube is less than 45º). Fruits with fully formed seeds may not be mature with respect to taxonomically important characters of fruit size and color. Ripe fruits are those that abscise easily from the plant with a gentle tug (although fruits of Coryphantha robustispina sometimes require a hard pull). A pitted seed testa is easily viewed with a hand lens. A weakly raised-reticulate seed testa is distinguishable from a smooth testa only with a lens (10× or greater magnification). A reticulate color pattern alone does not imply that the anticlinal cell walls actually protrude.
Selected References
Lower Taxa
Key
1 | Spines peglike, not sharply pointed, proximally compressed laterally; radial spines 5 mm or less; stems 1-2.7 × 0.6-1.7(-2.5) cm | Coryphantha minima |
1 | Spines needlelike, sharp pointed, terete or compressed dorsiventrally or laterally; radial spines mostly 6-35(-50) mm (rarely as short as 4 or 5 mm in C. chaffeyi, C. duncanii, C. missouriensis, C. robertii, C. sneedii, C. tuberculosa); stems 2.5-27 × (1-)1.5-15 cm | > 2 |
2 | In sexually mature plants areolar groove extending 1/2-3/4 of distance from spine cluster to axil of tubercle; stem cortex mucilaginous; inner tepals rose-pink to magenta | Coryphantha macromeris |
2 | In sexually mature plants areolar groove connecting spine clusters and axils of tubercles; stem cortex usually not mucilaginous; inner tepals yellowish, whitish, greenish, pink, or purple | > 3 |
3 | Seeds smooth or weakly raised-reticulate, brown when dry, red or yellow when fresh; outer tepals entire, denticulate, or minutely fringed | > 4 |
3 | Seeds pitted, black or brown when dry, black, brown, red, or yellow when fresh; outer tepals fringed | > 10 |
4 | Inner tepals pink to deep rose-purple with white proximal zone; seeds 1-1.5 mm | Coryphantha ramillosa |
4 | Inner tepals yellow, turning pinkish or reddish only in wilted or day-old flowers, proximally red, yellow, or greenish yellow; seeds 1.7-3 mm | > 5 |
5 | Tubercles (10-)15-30(-40) mm; fruits (35-)42(-52) mm; longest central spines, when present, 23-34 mm, hooked or straight to strongly curved | Coryphantha robustispina |
5 | Tubercles 6-15 mm; fruits 9-28 mm; longest central spines 9-25 mm, only straight or curved throughout their lengths | > 6 |
6 | Flowers distant from stem apex, forming ring around stem; Arizona and Mexico | Coryphantha recurvata |
6 | Flowers apical or nearly so, only fruits sometimes displaced away from stem apex by growth of new tubercles after flowering; Texas and Mexico | > 7 |
7 | Flowers lacking red in centers | > 8 |
7 | Flowers red centered, or at least with filaments partly red | > 9 |
8 | Stigma lobes white or cream; inner tepals pale yellow; pith occupying 1/2 of lesser stem diam.; medullary vascular system conspicuous; near Laredo, Texas | Coryphantha nickelsiae |
8 | Stigma lobes whitish or greenish yellow; inner tepals bright yellow; pith occupying 1/4-1/3 of lesser stem diam.; medullary vascular system absent; mostly w of Pecos River, Texas | Coryphantha echinus |
9 | Spines 16-34 per areole; tubercles firm; mostly w of Pecos River, Texas | Coryphantha echinus |
9 | Spines 9-16(-18) per areole; tubercles soft or flaccid; e of Pecos River, Texas | Coryphantha sulcata |
10 | Floral remnant on fruit deciduous; spines 6-20 per areole; stems deep-seated in substrate, often nearly subterranean except in growing season [segregate genus Neobesseya] | > 11 |
10 | Floral remnant on fruit persistent; spines (10-)15-76(-95) per areole; stems usually not deep-seated, more than 1/2 above ground (sometimes deep-seated and flat-topped in winter in C. hesteri and C. vivipara) [segregate genus Escobaria] | > 12 |
11 | Spine-bearing areoles with long, white wool, making areoles appear unusually large, obscuring basal portions of spines; restricted distribution, se Arizona near Mexican boundary | Coryphantha robbinsorum |
11 | Spine-bearing areoles with short, white wool, 1-3 mm, shorter with age making areoles appear normal size, not obscuring spine bases; widespread from c Arizona northward and eastward | Coryphantha missouriensis |
12 | Central spines erect, appressed and therefore inconspicuous against adaxial radial spines (i.e., abaxial or "inner" central spines absent) | > 13 |
12 | Central spines radiating in every direction and not confined to adaxial parts of spine clusters, or principal central spine in each areole porrect and conspicuous | > 15 |
13 | Spines (21-)31-44(-55) per areole; stigma lobes dark green to bright yellow; seeds black; fruit bright red | Coryphantha duncanii |
13 | Spines (12-)15-20(-25) per areole; stigma lobes white (to pink or purple); seeds brown; fruit green to dull reddish | > 14 |
14 | Central spines, when present, 9.5-13(-15) mm; roots fleshy, enlarged taproots, basally 1/3-1/2 of stem diam.; fruits (3.5-)5-8(-10) × 3-6 mm, quickly drying; seeds dark brown, spheric; above-ground portion of stem 1-6.5 (-9) cm; druses 0.3-0.5 mm diam | Coryphantha hesteri |
14 | Central spines 9-25 mm; roots ± diffuse, less than 1/4 of stem diam.; fruits 12-28 × 7-20 mm, juicy; seeds bright reddish brown, comma-shaped or nearly obovoid; above-ground portion of stem 2.5-20 cm; druses 0.7-1 mm diam | Coryphantha vivipara |
15 | Ripe fruit green or maroon to dull reddish pink (sometimes blood red or crimson in C. sneedii); stigma lobes pink, purple, or white; druses large, 0.5-1 mm diam., lenticular, present in older parts of the pith and cortex; widespread, w United States | > 16 |
15 | Ripe fruit red; stigma lobes green or white (rarely red); druses, when present, nearly microscopic, not lenticular; New Mexico, Texas | > 19 |
16 | Branches 0-250; inner tepals generally white, cream, pale tan, greenish white, or pale rose-pink; fruits either red color phase or green color phase; se New Mexico, w Texas | Coryphantha sneedii |
16 | Branches 0-30; inner tepals pale rose-pink to intense pink, pale dull creamy yellow, or pale greenish tan to pale yellow-orange, or pale apricot; fruits green, dull pink, or brownish red; widespread, California to Texas northward | > 17 |
17 | Stigma lobes widely spreading; s California | Coryphantha alversonii |
17 | Stigma lobes spreading, ascending, or recurved; California eastward | > 18 |
18 | Inner tepals ascending or recurved only at tips, pale dull creamy yellow or pale greenish tan to pale yellow-orange or pale apricot, usually with distinct darker midstripes | Coryphantha chlorantha |
18 | Inner tepals usually spreading, recurved, pale rose-pink to reddish pink or magenta throughout or with vaguely to sharply defined darker midstripes | Coryphantha vivipara |
19 | Stigma lobes white; anthers pale yellow, nearly white; sterile distal part of flower tube 5-8.5(-11) mm, longer than stamen-bearing part | Coryphantha tuberculosa |
19 | Stigma lobes green to bright yellow (rarely red); anthers bright yellow; sterile distal part of flower tube 0-2 mm, much shorter than the stamen-bearing part | > 20 |
20 | Stems branched, resulting in irregular masses of mostly immature stems that proliferate before reaching sexual maturity, clumps 10-30(-100) cm diam.; below 500 m elevation, e of Pecos River | Coryphantha robertii |
20 | Stems usually unbranched (rarely with 2-5 branches); 800-2500 m elevation, w of Pecos River | > 21 |
21 | Spines (35-)40-55(-81) per areole, white with reddish or yellowish tips | Coryphantha chaffeyi |
21 | Spines 26-42 per areole, white with dark tips | Coryphantha dasyacantha |