Erythranthe tilingii |
Erythranthe cinnabarina |
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larger mountain monkeyflower, mountain monkey-flower, Tiling's monkey-flower |
Arizona big red monkeyflower |
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Habit | Perennials, rhizomatous, solitary to weakly colonial, rhizomes forming a mass, yellowish, branching, filiform. | Perennials, rhizomatous. |
Stems | erect-ascending, usually freely branched, 2–35 cm, glabrous or sparsely stipitate-glandular to short glandular-villous. |
usually erect to ascending, freely branched, 25–60 cm, glabrous. |
Leaves | cauline; petiole 0–25 mm, distals 0 mm; blade palmately 3–5-veined, ovate to lanceolate-triangular or narrowly lanceolate (broadly ovate in large-leaved forms), 5–35(–55) mm, base cuneate to attenuate, margins irregularly denticulate, apex acute to obtuse or rounded, surfaces glabrous, sparsely stipitate-glandular to short glandular-villous, glabrate, or sparsely to moderately villous, hairs thick-vitreous, eglandular. |
usually cauline; petiole 0 mm; blade palmately veined, elliptic to oblong-elliptic, elliptic-lanceolate, or broadly lanceolate, 60–125 × 25–46 mm, base narrowly auriculate, clasping to subclasping, margins shallowly dentate, teeth sharp-pointed, apex acute, adaxial surface glabrous or minutely sessile- or stipitate-glandular along veins, lamina glabrous. |
Flowers | herkogamous, 1–3(–5), from distal nodes. |
herkogamous, 2–4(–8), axillary at leafy distal nodes. |
Styles | hirtellous. |
glabrous. |
Corollas | yellow, red-dotted, bilaterally symmetric, bilabiate; tube-throat broadly funnelform, 15–28 mm, exserted 5–10 mm beyond calyx margin; limb expanded 14–30 mm. |
deep orange, dull orange, red-orange, or deep scarlet, throat yellow-orange, dark red stripes leading onto basal part of lobes, not spotted, palate ridges red, bilaterally symmetric, strongly bilabiate; tube-throat tubular, 29–36 mm, exserted 7–12 mm beyond calyx margin; throat open, palate ridges densely short-villous, hairs yellowish. |
Fruiting pedicels | 15–35(–40) mm, sparsely stipitate-glandular to short glandular-villous. |
50–95 mm. |
Fruiting calyces | usually purple-tinged and purple-dotted, broadly campanulate, inflated, sagittally compressed, 11–15 mm, glabrous or sparsely stipitate-glandular to short glandular-villous, villous at sinuses, throat closing, lobes broadly ovate, abaxial usually longer than lateral, adaxial at least 2 times as long as others. |
cylindric-campanulate, not inflated, (27–)29–34 mm, minutely stipitate- or sessile-glandular, lobes 7–10 mm, ovate, apex abruptly attenuate to linear-caudate. |
Capsules | included, 5–7 mm. |
included, 14–18 mm. |
Anthers | included, glabrous. |
exserted, white-villous, thecae spreading. |
2n | = 28, 56. |
= 16. |
Erythranthe tilingii |
Erythranthe cinnabarina |
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Phenology | Flowering Jul–Sep. | Flowering Jun–Aug(–Sep). |
Habitat | Seeps, springs, stream banks, shallow rivulets, cliff bases, ledges and crevices, steep gravelly slopes, wet meadows. | Canyons, ravines, streambeds and margins, riparian vegetation, mixed conifer forest. |
Elevation | 1400–3400 m. (4600–11200 ft.) | 2100–3300 m. (6900–10800 ft.) |
Distribution |
AZ; CA; ID; MT; NV; OR; UT; AB
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AZ |
Discussion | Plants of Erythranthe tilingii are characterized by their relatively low stature and stems arising from a system of thin rhizomes and producing mostly one to three large flowers each; they usually occur at relatively high elevations. Erythranthe tilingii sometimes has been considered to include one or several infraspecific entities; from within this taxonomic amalgam, four distinct species are recognized here: E. caespitosa, E. corallina, E. minor, and E. tilingii. Erythranthe corallina and E. minor probably are more closely related to E. guttata. The populations identified here as E. tilingii from northeastern Oregon northeast to Alberta and southeast to Utah may prove to be a separate (undescribed) species. Erythranthe tilingii in the strict sense is relatively widespread over the western United States and is sympatric with E. caespitosa and E. corallina. Leaves in E. tilingii are variable in size, and particularly in Idaho, they may approach the small size of those of E. caespitosa, but the leaf margins of E. tilingii are distinctly toothed, and the stems are taller and more erect. Across the range of the species, plants sometimes produce very large leaves, but these often occur on plants with characteristically smaller leaves. This wide variability in size apparently does not occur in E. caespitosa. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Erythranthe cinnabarina is similar to typical E. cardinalis in its spreading anther thecae, relatively short-exserted corolla tube, and its reflexing corolla lobes but distinct in its generally larger leaves with reduced vestiture, fewer flowers, larger calyx and corolla, apically caudate calyx lobes, and its separate geographical range. Erythranthe cinnabarina occurs in Cochise County (Chiricahua Mountains), Graham County (Pinaleño Mountains), and Pima County (Santa Catalina Mountains). Erythranthe verbenacea, with which it sometimes has been confused, occurs at lower elevations (350–2600 m) and ranges over most of the state (Apache, Cochise, Coconino, Gila, Graham, La Paz, Maricopa, Mohave, Pima, Pinal, Santa Cruz, and Yavapai counties). Erythranthe cinnabarina apparently occurs alone (without E. verbenacea) in the Pinaleño Mountains and in the Chiricahua Mountains, but both species have been abundantly documented in the Santa Catalina Mountains, where they sometimes closely co-occur in areas of elevational overlap (for example, at Marshall Gulch, about 2500 m; at Bear Wallow Campground, about 2600 m). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 17, p. 408. | FNA vol. 17, p. 393. |
Parent taxa | Phrymaceae > Erythranthe | Phrymaceae > Erythranthe |
Sibling taxa | ||
Synonyms | Mimulus tilingii, M. caespitosus var. implexus, M. implexus, M. implicatus, M. langsdorffii var. tilingii, M. lucens, M. veronicifolius | |
Name authority | (Regel) G. L. Nesom: Phytoneuron 2012-39: 44. (2012) | G. L. Nesom: Phytoneuron 2014-31: 16, figs. 16, 17. (2014) |
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