Erythranthe norrisii |
Erythranthe chinatiensis |
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Kaweah monkeyflower, Norris' monkeyflower |
Chinati Mountains monkeyflower |
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Habit | Annuals, fibrous-rooted or filiform-taprooted. | Perennials, rhizomatous, sometimes rooting at nodes, mat-forming. |
Stems | ascending to erect-ascending, geniculate at nodes, usually branched from proximal nodes, 2–15(–25) cm, villous-glandular. |
procumbent, branched, 5–20 cm, glabrous. |
Leaves | basal and cauline; petiole 5–10(–15) mm; blade palmately 3–5-veined, sometimes with 1–3 distal vein pairs diverging pinnately, elliptic to elliptic-obovate, 20–35 × 10–20 mm, base usually attenuate, margins subentire to distally denticulate, apex acute to obtuse, surfaces villous-glandular. |
cauline; petiole 2–10(–20) mm; blade palmately 3–5(–7)-veined, ovate to broadly ovate or orbicular-ovate, 4–15(–22) × 4–15(–18) mm, base truncate to cuneate, margins shallowly denticulate or merely mucronate to mucronulate, teeth 3–6 per side, apex acute to obtuse, surfaces glabrous, adaxial sometimes moderately villosulous, hairs vitreous, flattened, eglandular or minutely gland-tipped. |
Flowers | herkogamous, 1–5, from medial to distal nodes. |
plesiogamous, 2–8, axillary at distal nodes. |
Styles | glabrous. |
glabrous. |
Corollas | yellow, base of each lobe with a prominent maroon splotch, abaxial limb with white patch at 2 sinus bases, weakly bilaterally or radially symmetric, weakly bilabiate or regular; tube-throat cylindric-funnelform, 12–16 mm, exserted beyond calyx margin; limb expanded 15–30 mm, lobes oblong-obovate to orbicular-obovate, apex rounded-truncate. |
yellow, red-dotted, bilaterally symmetric, bilabiate; tube-throat funnelform, 7–8 mm, exserted beyond calyx margin; limb expanded 6–7 mm, abaxial limb strongly reflexed, lobes fimbriate. |
Fruiting pedicels | 20–35(–50) mm, villous-glandular. |
10–20 mm, glabrous. |
Fruiting calyces | red-dotted, campanulate, weakly inflated, 4–6 mm, margins distinctly toothed or lobed, villous-glandular, ribs rounded-thickened, lobes pronounced, erect, often incurved, linear-oblong to oblong-lanceolate, apex rounded to blunt. |
nodding 45–90º, 5-lobed, ellipsoid, inflated, sagittally compressed, 5–6 mm, glabrous or sparsely villosulous-glandular, throat closing. |
Capsules | usually slightly exserted, 4–6 mm. |
included, 4–5 mm. |
Anthers | included, glabrous. |
included, glabrous. |
2n | = 32. |
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Erythranthe norrisii |
Erythranthe chinatiensis |
|
Phenology | Flowering Mar–May. | Flowering Feb–Sep. |
Habitat | Steep marble outcrops in soil pockets, moss covered marble and quartzite ledges, cracks, fractures, weathered faces, chamise chaparral or blue oak woodlands. | Seeps in vertical cliff faces, wet bluffs. |
Elevation | 300–1300 m. (1000–4300 ft.) | 600–1900(–2300) m. (2000–6200(–7500) ft.) |
Distribution |
CA
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TX |
Discussion | Erythranthe norrisii is known only from the Kaweah River drainage; most populations are in Sequoia National Park in Tulare County. The species is characterized by its short-petiolate leaves with attenuate bases, very large corollas with red splotches at the base of each lobe and two white patches on the abaxial limb, and very short, purple-dotted calyces with rounded-thickened ribs and linear-oblong lobes incurved in fruit. The capsules often are slightly exserted. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Erythranthe chinatiensis is similar to E. parvula in its prostrate habit, five-lobed calyces, and fimbriate corolla lobes. It differs from the latter in its nearly glabrous leaves and strongly reflexed abaxial corolla lip. Erythranthe chinatiensis is known only from Presidio County but should be expected to occur also in adjacent Chihuahua, Mexico. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 17, p. 405. | FNA vol. 17, p. 424. |
Parent taxa | Phrymaceae > Erythranthe | Phrymaceae > Erythranthe |
Sibling taxa | ||
Synonyms | Mimulus norrisii | |
Name authority | (Heckard & Shevock) G. L. Nesom: Phytoneuron 2012-39: 39. (2012) | G. L. Nesom: Phytoneuron 2012-40: 86, figs. 12–14. (2012) |
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