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mimule musqué, musk monkeyflower, musk-flower, musk-plant, sticky monkey-flower

Willis' monkeyflower

Habit Perennials, rhizomatous, rooting at proximal nodes. Perennials, rhizomatous, rarely rooting at proximal nodes, usually forming large colonies, rhizomes white, usually highly branching.
Stems

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.

usually sprawling-decumbent, branched, sometimes simple, 7–45 cm, nodes (2–)4–15+, densely glandular-villous, hairs 1–2 mm, glandular, internodes evident.

Leaves

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.

usually cauline, basal not persistent, distinctly separated;

petiole 0 mm, sometimes 1–2 mm at proximal nodes;

blade bicolored, purplish abaxially, pinnately veined, ovate to elliptic-ovate, midcauline 10–35 × 6–18 mm, base rounded to subcordate, margins coarsely serrate-dentate to denticulate or subentire, apex short-attenuate to acute, obtuse, or rounded, surfaces densely glandular-villous, hairs 1–2 mm, gland-tipped.

Flowers

herkogamous, 1–8, from medial to distal nodes.

herkogamous, (4–)8–30+, from medial to distal nodes, sometimes from all nodes.

Styles

glabrous.

glabrous.

Corollas

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.

yellow, throat, tube, and proximal portion of abaxial 3 lobes with fine, red to brownish lines, weakly bilaterally or nearly radially symmetric, weakly bilabiate or nearly regular;

tube-throat narrowly funnelform, 12–15 mm, exserted beyond calyx margin;

limb 9–12 mm wide (pressed), lobes oblong-obovate, apex rounded to notched.

Fruiting pedicels

(7–)10–25 mm, glabrate to glandular-villous.

4–20(–25) mm, densely glandular-villous, hairs 1–2 mm, gland-tipped.

Fruiting calyces

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.

ridge- to wing-angled, campanulate to cylindric-campanulate, weakly inflated, 7–10 mm, densely glandular-villous, lobes erect to slightly spreading, unequal, triangular to linear-lanceolate, 2–4 mm, apex acuminate-apiculate.

Capsules

included, 6–8 mm.

included, 4–5 mm.

Anthers

included, glabrous or slightly hirtellous to scabrous.

included, glabrous or finely hirtellous to scabrous.

2n

= 32.

Erythranthe moschata

Erythranthe willisii

Phenology Flowering May–Aug. Flowering May–Sep.
Habitat 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. Seepage, drainage margins, moist soils, talus, cracks and crevices, soils deprived from serpentine.
Elevation (300–)400–3100 m. ((1000–)1300–10200 ft.) (500–)700–900 m. ((1600–)2300–3000 ft.)
Distribution
from FNA
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]
[WildflowerSearch map]
from FNA
CA
Discussion

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.)

Erythranthe willisii is narrowly endemic over serpentine along the North Fork Feather River (including the North Branch) in Plumas County. In the original description, its range was said to include serpentine localities in closely adjacent areas of east-central Butte, Plumas, and northwestern Yuba counties, but subsequent field work has shown that these peripheral populations are E. moschata, and that E. willisii occurs only in the bottom of the Serpentine Canyon area. The most consistent and recognizable features of E. willisii are the long, sprawling stems often spread over a large area, sometimes reaching at least 45 cm and often with many crowded nodes, sessile or subsessile leaves with rounded to subcordate bases, and short pedicels, characteristically no longer than the subtending leaves (except sometimes the distal ones where subtending leaves are distinctly reduced in size). It is possible that stem growth in E. willisii is indeterminate versus determinate in E. moschata. Sessile to subsessile leaves occur in E. moschata, especially in the California Sierra Nevada, but petiole length and leaf base shape are variable within populations; lack of petioles and a rounded/subcordate base are fixed characters in E. willisii (as they are also in E. ptilota). Although large colonies of E. moschata are sometimes encountered, the individual plants tend to be erect (in California) and with few distal flowers. In the field, the dense vestiture of E. willisii is a prominent feature, but this is harder to distinguish in pressed specimens, and there is a strong tendency for purple abaxial leaf coloration in E. willisii. Phenology and flower morphology of E. willisii and E. moschata appear to be similar, but E. moschata in north-central California does not occur at as low elevations as E. willisii.

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

Source FNA vol. 17, p. 401. FNA vol. 17, p. 401.
Parent taxa Phrymaceae > Erythranthe Phrymaceae > Erythranthe
Sibling taxa
E. acutidens, E. alsinoides, E. ampliata, E. androsacea, E. arenaria, E. arenicola, E. arvensis, E. barbata, E. bicolor, E. brachystylis, E. breviflora, E. breweri, E. caespitosa, E. calcicola, E. calciphila, E. cardinalis, E. carsonensis, E. charlestonensis, E. chinatiensis, E. cinnabarina, E. corallina, E. cordata, E. decora, E. dentata, E. diffusa, E. discolor, E. eastwoodiae, E. erubescens, E. exigua, E. filicaulis, E. filicifolia, E. floribunda, E. gemmipara, E. geniculata, E. geyeri, E. glaucescens, E. gracilipes, E. grandis, E. grayi, E. guttata, E. hallii, E. hardhamiae, E. hymenophylla, E. inamoena, E. inconspicua, E. inflatula, E. jungermannioides, E. laciniata, E. latidens, E. lewisii, E. linearifolia, E. marmorata, E. michiganensis, E. microphylla, E. minor, E. montioides, E. nasuta, E. norrisii, E. nudata, E. palmeri, E. pardalis, E. parishii, E. parvula, E. patula, E. percaulis, E. primuloides, E. ptilota, E. pulsiferae, E. purpurea, E. regni, E. rhodopetra, E. rubella, E. scouleri, E. shevockii, E. sierrae, E. suksdorfii, E. taylorii, E. thermalis, E. tilingii, E. trinitiensis, E. unimaculata, E. utahensis, E. verbenacea, E. washingtonensis, E. willisii
E. acutidens, E. alsinoides, E. ampliata, E. androsacea, E. arenaria, E. arenicola, E. arvensis, E. barbata, E. bicolor, E. brachystylis, E. breviflora, E. breweri, E. caespitosa, E. calcicola, E. calciphila, E. cardinalis, E. carsonensis, E. charlestonensis, E. chinatiensis, E. cinnabarina, E. corallina, E. cordata, E. decora, E. dentata, E. diffusa, E. discolor, E. eastwoodiae, E. erubescens, E. exigua, E. filicaulis, E. filicifolia, E. floribunda, E. gemmipara, E. geniculata, E. geyeri, E. glaucescens, E. gracilipes, E. grandis, E. grayi, E. guttata, E. hallii, E. hardhamiae, E. hymenophylla, E. inamoena, E. inconspicua, E. inflatula, E. jungermannioides, E. laciniata, E. latidens, E. lewisii, E. linearifolia, E. marmorata, E. michiganensis, E. microphylla, E. minor, E. montioides, E. moschata, E. nasuta, E. norrisii, E. nudata, E. palmeri, E. pardalis, E. parishii, E. parvula, E. patula, E. percaulis, E. primuloides, E. ptilota, E. pulsiferae, E. purpurea, E. regni, E. rhodopetra, E. rubella, E. scouleri, E. shevockii, E. sierrae, E. suksdorfii, E. taylorii, E. thermalis, E. tilingii, E. trinitiensis, E. unimaculata, E. utahensis, E. verbenacea, E. washingtonensis
Synonyms 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 (Douglas ex Lindley) G. L. Nesom: Phytoneuron 2012-39: 38. (2012) G. L. Nesom: Phytoneuron 2017-17: 7, figs. 14–22. (2017)
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