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larger mountain monkeyflower, mountain monkey-flower, Tiling's monkey-flower

Colorado monkeyflower

Habit Perennials, rhizomatous, solitary to weakly colonial, rhizomes forming a mass, yellowish, branching, filiform. Perennials, rhizomatous, colonial, rhizomes forming a mass, branching, filiform.
Stems

erect-ascending, usually freely branched, 2–35 cm, glabrous or sparsely stipitate-glandular to short glandular-villous.

erect to erect-ascending, branched, 5–20 cm, densely minutely hirtellous and eglandular or with a mixture of hirtellous and gland-tipped hairs.

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.

basal and cauline;

petiole 0 mm or proximals 1–3 mm;

blade palmately 3-veined, broadly ovate to elliptic-ovate or lanceolate, 8–25 × 5–15 mm, base cuneate to truncate, margins shallowly dentate to denticulate, apex acute to obtuse, surfaces glabrous.

Flowers

herkogamous, 1–3(–5), from distal nodes.

herkogamous, 1–3, from distal nodes.

Styles

hirtellous.

sparsely hirtellous.

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.

yellow, not red-dotted, bilaterally symmetric, bilabiate;

tube-throat tubular-funnelform, 9–11 mm, exserted 0–1(–2) mm beyond calyx margin.

Fruiting pedicels

15–35(–40) mm, sparsely stipitate-glandular to short glandular-villous.

10–20 mm, densely minutely hirtellous and eglandular or with a mixture of hirtellous and gland-tipped hairs.

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.

nodding 80–100º, not purple-dotted, cylindric-campanulate, inflated, sagittally compressed, 10–13 mm, densely minutely hirtellous and eglandular or with a mixture of hirtellous and gland-tipped hairs, throat closing.

Capsules

included, 5–7 mm.

included, 5–8 mm.

Anthers

included, glabrous.

included, glabrous.

2n

= 28, 56.

Erythranthe tilingii

Erythranthe minor

Phenology Flowering Jul–Sep. Flowering Jul–Aug(–Sep).
Habitat Seeps, springs, stream banks, shallow rivulets, cliff bases, ledges and crevices, steep gravelly slopes, wet meadows. Stream and lake edges, intermittent subalpine water courses, roadside ditches, subalpine to alpine.
Elevation 1400–3400 m. (4600–11200 ft.) 3000–3700 m. (9800–12100 ft.)
Distribution
from FNA
AZ; CA; ID; MT; NV; OR; UT; AB
[WildflowerSearch map]
from FNA
CO; NM
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.)

The corollas of Erythranthe minor are shorter than those of typical E. tilingii, and the two species are allopatric. Corollas of E. tilingii rarely may be equally as short as those of E. minor but are produced in scattered localities on plants that are depauperate in other ways. The range of E. minor is primarily in Colorado apparently extending southward into the Wheeler Peak area of Taos County, New Mexico. Attribution of its range into the La Sal Mountains of east-central Utah has been based on misidentifications of E. guttata; the distinction between E. guttata and E. minor in Colorado also needs clarification.

Mimulus luteus Linnaeus var. alpinus A. Gray (1863, the type from Colorado) is an illegitimate name for Erythranthe minor, preceded by M. luteus var. alpinus Lindley (1827).

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

Source FNA vol. 17, p. 408. FNA vol. 17, p. 409.
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. 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. 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. 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, E. willisii
Synonyms Mimulus tilingii, M. caespitosus var. implexus, M. implexus, M. implicatus, M. langsdorffii var. tilingii, M. lucens, M. veronicifolius Mimulus minor, M. alpinus, M. langsdorffii var. alpinus, M. langsdorffii var. minor
Name authority (Regel) G. L. Nesom: Phytoneuron 2012-39: 44. (2012) (A. Nelson) G. L. Nesom: Phytoneuron 2012-39: 44. (2012)
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