The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

Veatch's blazing star, white-stem blazingstar, white-stem stick-leaf

blazing-star, mentzelia, stick-leaf

Habit Plants candelabra-form, (5–)20–50 cm. Herbs or subshrubs [shrubs or trees], annual, biennial, or perennial; trichomes (1) pointed with surfaces ± smooth or antrorsely barbed and (2) retrorsely barbed along shaft and at apex or only at apex.
Stems

erect, clambering, or decumbent.

Leaves

basal and cauline or cauline;

petiole present or absent;

blade hastate, deltate, cordate, ovate, elliptic, lanceolate, linear, spatulate, oblanceolate, obovate, or orbiculate, lobed or unlobed, margins dentate, serrate, crenate, or entire.

Basal leaves

persisting;

petiole present or absent;

blade linear-lanceolate, margins deeply to shallowly lobed.

Cauline leaves

petiole absent;

blade ovate-lanceolate to lanceolate, to 17 cm, margins usually deeply lobed to dentate, rarely entire.

Bracts

usually green with prominent white base usually conspicuously extending outwards from midvein, rarely green, usually ovate, rarely lanceolate, 3.3–6.2 × 1.5–3.2 mm, width 1/4–7/8 length, not concealing capsule, margins usually 3–7-lobed, rarely entire.

Inflorescences

dichasia or flowers solitary;

peduncle inconspicuous.

Pedicels

not elongating in fruit.

Flowers

sepals 2–5 mm;

petals red to orange proximally, orange to yellow distally, 4–7(–10) mm, apex retuse;

stamens 20+, 3–7 mm, filaments monomorphic, filiform, unlobed;

styles (3–)3.5–6 mm.

hypanthium adnate to ovary proximally, free distally;

perianth whorls differentiated;

sepals green, connate basally, lanceolate to narrowly ovate, shorter than petals;

petals white, yellow, or orange, sometimes red proximally, distinct or connate basally, spatulate, ovate, elliptic, oblanceolate, or obovate, spreading to erect, glabrous or hairy abaxially, on margins, or on apices;

nectary distal on ovary;

stamens 8–45+, exserted or included;

filaments monomorphic, filiform or dorsiventrally flattened and linear, or heteromorphic, outer dorsiventrally flattened and linear, elliptic, spatulate, or oblanceolate [lanceolate], inner filiform or dorsiventrally flattened and linear, longer than anthers;

anthers without distal connective extension;

staminodes present or absent;

pistil 3-carpellate (5–7-carpellate in M. decapetala), placentae parietal;

stigma lingulate, 3-lobed (5–7-lobed in M. decapetala), papillate.

Fruits

capsules, dehiscing by apical valves [splitting longitudinally], cup-shaped, lingulate, subcylindric, cylindric, ovoid, urceolate, clavate, or funnelform, straight or curved, sometimes S-shaped;

sepals persistent.

Capsules

clavate, 8–28 × 2–4 mm, axillary curved to 70° at maturity, usually inconspicuously longitudinally ribbed.

Seeds

15–35, in 2+ rows distal to mid fruit, tan, dark-mottled, usually irregularly polygonal, occasionally triangular prisms proximal to mid fruit, surface tuberculate under 10x magnification; recurved flap over hilum absent;

seed coat cell outer periclinal wall domed, domes on seed edges more than or equal to 1/2 as tall as wide at maturity.

(1–)2–60+, ovoid, oblong, bottle-shaped, pyriform, irregularly polygonal, or trigonal prisms, dorsiventrally flattened or not, 0.5–4.5 mm, winged or not winged.

x

= 9.

2n

= 54.

Mentzelia veatchiana

Mentzelia

Phenology Flowering Mar–Jun.
Habitat Loamy to sandy soils, grasslands, desert scrub, oak-pine woodlands.
Elevation 200–2500 m. (700–8200 ft.)
Distribution
from FNA
AZ; CA; NV; OR
[WildflowerSearch map]
[BONAP county map]
from USDA
w North America; Mexico; Central America; South America; c North America; se North America; West Indies
[BONAP county map]
Discussion

Mentzelia veatchiana is the most common and widely distributed hexaploid species in sect. Trachyphytum. It exhibits considerable morphological variation and can be difficult to distinguish from M. montana in northern California. Like the larger-flowered M. pectinata, M. veatchiana has interfertile populations with petal colors ranging from orange to yellow (J. E. Zavortink 1966). When bearing orange petals, M. veatchiana is easily distinguished from other species. Reports of M. veatchiana from Utah are based on specimens treated here as M. montana.

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

Species ca. 95 (85 in the flora).

Mentzelia is monophyletic and sister to subfam. Gronovioideae (M. L. Moody et al. 2001; L. Hufford et al. 2003). These studies recovered clades that correspond to the six described sections of Mentzelia, including the five treated here and the monospecific sect. Dendromentzelia Urban & Gilg, which consists only of M. arborescens Urban & Gilg of Michoacán and Oaxaca, Mexico.

Mentzelias in North America often are ruderal or found in low-productivity, disturbance-prone environments, such as arroyos, sand dunes, cliffs, or talus slopes. They frequently are associated with distinctive substrates, including gypsum, limestone, serpentine, or volcanic tuff, and some might be edaphically restricted (J. B. Glad 1976; H. J. Thompson and A. M. Powell 1981; C. M. Christy 1997; N. H. Holmgren and P. K. Holmgren 2002; Brokaw et al. 2015).

Changes in chromosome number, through both aneuploidy and polyploidy, have been important in the evolution of Mentzelia. Aneuploidy has been especially important in reproductive isolation in sections Bartonia (haploid chromosome numbers include 9, 10, 11, and 18) and Bicuspidaria (haploid chromosome numbers include 9, 10). In contrast, aneuploidy has not been found in sections Mentzelia or Trachyphytum, although polyploidy has been found in both. In sect. Mentzelia, polyploidy has been reported only in M. asperula. Polyploidy has played a more important role in reproductive isolation and diversification in sect. Trachyphytum, in which diploids, tetraploids, hexaploids, and octoploids have been reported (H. J. Thompson and H. Lewis 1953).

Floral forms differ among the sections of Mentzelia, which may be indicative of reproductive shifts that were important in the differentiation of the sectional lineages. Reproductive ecology has been investigated best in sect. Bicuspidaria, in which Xeralictus bicuspidariae, a robust oligolectic bee, is the main pollinator of M. hirsutissima, M. tricuspis, M. tridentata, and is one of three main pollinators of M. involucrata (G. S. Daniels 1970). Only M. reflexa, which has markedly different flowers compared to other species of sect. Bicuspidaria, is not pollinated by X. bicuspidariae. Instead, another oligolectic bee, Perdita koebelei, is its primary pollinator (Daniels). Bees have been suggested to be the primary pollinators of other sections of Mentzelia, except for the few large-flowered species of sect. Bartonia in which hawk moth pollination has been observed (H. J. Thompson 1960; A. R. Moldenke 1976; R. J. Hill 1977). Many polyploid species of sect. Trachyphytum have small flowers and reportedly self-fertilize (J. E. Zavortink 1966).

Seed surface features are important in Mentzelia taxonomy. In sections Dendromentzelia, Mentzelia, and Micromentzelia, which compose a basal grade in Mentzelia, seed coat cells are longer than wide. In contrast the derived clade consisting of sections Bartonia, Bicuspidaria, and Trachyphytum has seed coat cells that are polygonal and largely isodiametric. The shapes of anticlinal and outer periclinal walls of seed coat cells are similar in sections Bicuspidaria and Trachyphytum but differ among the other sections of North American species. Seed coat cell anticlinal wall shape, which is particularly useful in distinguishing species in sect. Bartonia, may be straight, wavy (curves along walls forming less than 45° angles), or sinuous (curves along walls forming at least 45° angles, often forming U-shaped undulations).

Leaf and bract margins in Mentzelia usually are toothed or lobed to some degree, ranging from serrate or dentate (divided relatively shallowly) through pinnate (defined here as divided partway to the midvein) to pinnatisect (divided nearly or to the midvein).

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

Key
1. Stamen filaments all or mostly distally 2-lobed.
sect. Bicuspidaria
1. Stamen filaments unlobed, or 5 outermost distally 2-lobed and 5–15 inner filaments unlobed (Mentzelia micrantha, sect. Trachyphytum).
→ 2
2. Stamen filaments dorsiventrally flattened, 1–3(–5) outermost petaloid; seeds not winged.
sect. Bicuspidaria
2. Stamen filaments filiform or outer dorsiventrally flattened, inner filiform, 0 or 5+ outermost petaloid, if 5+, seeds winged.
→ 3
3. Ovules and seeds oriented perpendicular to long axis of ovary; seeds winged; 5 outermost stamen filaments usually petaloid, sometimes not.
sect. Bartonia
3. Ovules and seeds oriented parallel to long axis of ovary; seeds not winged (occasionally winged in Mentzelia lindleyi); 5 outermost stamen filaments not petaloid.
→ 4
4. Plants perennial.
→ 5
5. Leaf blades, at least some, with broad basal lobes, margins flat; capsules usually subcylindric, clavate, lingulate, or funnelform, sometimes ovoid; seeds oblong, ovoid, or pyriform, coat cells oblong.
sect. Mentzelia
5. Leaf blades without broad basal lobes, margins revolute; capsules ovoid to urceolate; seeds ovoid to bottle-shaped, coat cells polygonal.
sect. Micromentzelia
4. Plants annual.
→ 6
6. Leaf blades, at least some, with broad basal lobes; seeds oblong, ovoid, or pyriform, dorsiventrally flattened to trigonal, coat cells oblong, much longer than wide, anticlinal walls sinuous; basal rosette of leaves absent, proximalmost internodes 10+ mm.
sect. Mentzelia
6. Leaf blades without broad basal lobes; seeds triangular prisms or irregularly polygonal, coat cells polygonal, ± isodiametric, anticlinal walls straight; basal rosette of leaves present, persistent or not, proximalmost internodes to 5 mm.
sect. Trachyphytum
Source FNA vol. 12, p. 543. FNA vol. 12, p. 496. Authors: Larry Hufford, John J. Schenk, Joshua M. Brokaw.
Parent taxa Loasaceae > Mentzelia > sect. Trachyphytum Loasaceae
Sibling taxa
M. affinis, M. albescens, M. albicaulis, M. argillicola, M. argillosa, M. aspera, M. asperula, M. candelariae, M. canyonensis, M. chrysantha, M. collomiae, M. congesta, M. conspicua, M. crocea, M. cronquistii, M. decapetala, M. densa, M. desertorum, M. dispersa, M. eremophila, M. filifolia, M. floridana, M. flumensevera, M. goodrichii, M. gracilenta, M. hirsutissima, M. holmgreniorum, M. hualapaiensis, M. humilis, M. integra, M. involucrata, M. inyoensis, M. isolata, M. jonesii, M. laciniata, M. laevicaulis, M. lagarosa, M. leucophylla, M. librina, M. lindheimeri, M. lindleyi, M. longiloba, M. marginata, M. memorabilis, M. mexicana, M. micrantha, M. mollis, M. monoensis, M. montana, M. multicaulis, M. multiflora, M. nitens, M. nuda, M. obscura, M. oligosperma, M. oreophila, M. pachyrhiza, M. packardiae, M. paradoxensis, M. pectinata, M. perennis, M. polita, M. procera, M. pterosperma, M. puberula, M. pumila, M. ravenii, M. reflexa, M. reverchonii, M. rhizomata, M. rusbyi, M. saxicola, M. shultziorum, M. sivinskii, M. speciosa, M. springeri, M. strictissima, M. thompsonii, M. tiehmii, M. todiltoensis, M. torreyi, M. tricuspis, M. tridentata, M. uintahensis
Subordinate taxa
M. sect. Bartonia, M. sect. Bicuspidaria, M. sect. Mentzelia, M. sect. Micromentzelia, M. sect. Trachyphytum
Synonyms M. albicaulis var. veatchiana
Name authority Kellogg: Proc. Calif. Acad. Sci. 2: 99, fig. 28. (1863) Linnaeus: Sp. Pl. 1: 516. (1753): Gen. Pl. ed. 5, 233. (1754)
Web links