Erythranthe caespitosa |
Erythranthe moschata |
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large mountain monkey-flower, mountain monkeyflower, Olympic monkeyflower, subalpine monkeyflower |
mimule musqué, musk monkeyflower, musk-flower, musk-plant, sticky monkey-flower |
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Habit | Perennials, rhizomatous, rooting at proximal nodes, sometimes producing creeping, small-leaved runners, forming matted colonies, rhizomes filiform. | Perennials, rhizomatous, rooting at proximal nodes. |
Stems | procumbent or decumbent to decumbent-ascending, delicate, usually in masses, terete or flattish, branched, 3–10 cm, glabrous, minutely hirtellous, or stipitate-glandular. |
erect, sometimes ascending to decumbent, simple or branched, (2–)5–20 cm, nodes 2–4(or 5), glabrate to glandular-villous, hairs 0.5–2 mm, gland-tipped, internodes evident. |
Leaves | basal and cauline; petiole: proximals 2–5 mm, distals 0 mm; blade often purple beneath, palmately 3-veined, orbicular to narrowly elliptic or ovate, proximals usually sublyrate, 3–12 mm, becoming larger distally, base cuneate to a short petiole, margins entire, mucronulate, or barely denticulate, apex obtuse, surfaces sparsely to moderately puberulent, hairs minute, stipitate-glandular. |
usually cauline, basal not persistent, distinctly separated; petiole 0 mm or (0.5–)1–5(–10) mm; blade pinnately veined, oblong-ovate to ovate, (10–)15–40(–50) × 5–25 mm, base obtuse-cuneate to truncate, rounded or subcordate, subclasping to sessile, margins coarsely serrate-dentate to denticulate or subentire, apex acute to obtuse, surfaces glabrate to glandular-villous. |
Flowers | herkogamous, 1–3, from distal nodes, commonly solitary. |
herkogamous, 1–8, from medial to distal nodes. |
Styles | minutely hirtellous. |
glabrous. |
Corollas | yellow, dark red-spotted, bilaterally symmetric, bilabiate; tube-throat broadly funnelform to cylindric-funnelform, 15–18 mm, exserted beyond calyx margin; abaxial limb with deflexed-spreading lobes, adaxial with ascending lobes, palate partially closed. |
yellow, throat with fine red to blackish or brown lines extending onto lobes, red to brown dots in throat and lobes present or absent, bilaterally or nearly radially symmetric, bilabiate or nearly regular; tube-throat narrowly funnelform, 11–18 mm, exserted beyond calyx margin; lobes oblong-obovate, apex rounded to notched. |
Fruiting pedicels | 10–30(–40) mm, sparsely to moderately villous, hairs short, gland-tipped, sometimes hirtellous. |
(7–)10–25 mm, glabrate to glandular-villous. |
Fruiting calyces | broadly campanulate, inflated, sagittally compressed, 7–15 mm, glabrous, minutely hirtellous, or stipitate-glandular, throat closing, proximalmost lobe pair upcurving, distalmost 3–5 mm, prominently protruding. |
ridge- to wing-angled, campanulate to cylindric-campanulate, weakly or not inflated, 6–13 mm, villous to glandular-villous, lobes erect to spreading-recurving, strongly unequal to subequal, triangular to linear-lanceolate or narrowly triangular-acuminate, 2–4 mm, apex acute to obtuse. |
Capsules | included, 4–5 mm. |
included, 6–8 mm. |
Anthers | included, glabrous. |
included, glabrous or slightly hirtellous to scabrous. |
2n | = 32. |
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Erythranthe caespitosa |
Erythranthe moschata |
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Phenology | Flowering Jul–Sep. | Flowering May–Aug. |
Habitat | Alpine meadows and slopes, stream banks, wet rocks in streams, wet crevices, talus. | Springs and seeps, creek edges, moist meadows, ditches, along trails, roadsides, rocky ridges, granite outcrops, shaded and wet places in sagebrush, aspen, fir, spruce-fir, lodgepole pine forests, meadows. |
Elevation | 1100–2000(–2300) m. (3600–6600(–7500) ft.) | (300–)400–3100 m. ((1000–)1300–10200 ft.) |
Distribution |
WA; BC
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CA; CO; CT; ID; MA; ME; MI; MT; NH; NJ; NV; NY; OR; PA; RI; UT; VA; VT; WA; WI; WV; WY; BC; NB; NF; NS; ON; PE; QC; SPM [Introduced in South America (Chile), Europe, e Asia (Japan), Pacific Islands (New Zealand), Australia]
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Discussion | Erythranthe caespitosa is endemic to northwestern and central Washington (Cascade and Olympic mountains) and adjacent British Columbia (Cascades, Selkirk Mountains and Chilliwack Valley, Coast Mountains). The plants have consistently small leaves with subentire margins, and the stems are consistently procumbent to decumbent-ascending, usually forming matted colonies. Erythranthe caespitosa and E. tilingii appear to be sympatric in counties of northwestern Washington, but this needs to be verified in the field. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Earlier segregation of Erythranthe moniliformis as distinct from E. moschata (for example, G. L. Nesom 2012g) emphasized a primarily erect habit and tendency toward sessile to subsessile and more densely arranged cauline leaves in E. moniliformis versus a decumbent to procumbent habit and consistently petiolate leaves on longer internodes in E. moschata. Discontinuities in morphology, geography, and ecology were not confirmed in later study by Nesom (2017). Rhizomes with small, tuberlike swellings can be observed over the whole moschata/moniliformis range, and there apparently are no consistent distinctions in vestiture and corolla size. Mimulus acutidens Reiche (1911), a later homonym of M. acutidens Greene, pertains here. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 17, p. 409. | FNA vol. 17, p. 401. |
Parent taxa | Phrymaceae > Erythranthe | Phrymaceae > Erythranthe |
Sibling taxa | ||
Synonyms | Mimulus scouleri var. caespitosus, M. caespitosus, M. tilingii var. caespitosus | Mimulus moschatus, E. inodora, E. moniliformis, M. crinitus, M. guttatus var. moschatus, M. inodorus, M. leibergii, M. macranthus, M. moniliformis, M. moschatus var. longiflorus, M. moschatus var. moniliformis, M. moschatus var. pallidiflorus |
Name authority | (Greene) G. L. Nesom: Phytoneuron 2012-39: 43. (2012) | (Douglas ex Lindley) G. L. Nesom: Phytoneuron 2012-39: 38. (2012) |
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