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

Rocky Mountain or petiole-purse monkeyflower

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

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

erect, straight at nodes, simple, 1–10 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.

cauline;

petiole 2–3 mm, laterally compressed, base deeply saccate, usually containing a lenticular propagule;

blade emerging from bulbils, palmately veined, elliptic-ovate to ovate, 2–8(–10) × 2–5(–7) mm, base truncate to shallowly cordate, margins entire or remotely denticulate, apex obtuse to rounded, surfaces glabrous.

Flowers

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

herkogamous, (1 or)2–12, from medial or medial to 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.

yellow, palate yellow, not spotted or striped, bilaterally symmetric, weakly bilabiate;

tube-throat broadly cylindric-funnelform, 3–4 mm, exserted beyond calyx margin;

lobes subequal, oblong-obovate, throat open, palate puberulent, abaxial ridges low.

Fruiting pedicels

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

4–6 mm, slightly longer than calyx, glabrous.

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.

strongly angled, subcampanulate, weakly inflated, 3–4 mm, margins distinctly toothed or lobed, glabrous, lobes pronounced, erect, incurved-triangular.

Capsules

included, 5–7 mm.

unknown.

Anthers

included, glabrous.

included, glabrous.

2n

= 28, 56.

= 16.

Erythranthe tilingii

Erythranthe gemmipara

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. Granitic seeps, thin soils over bedrock cliff bases, crevices, ledges, talus, among rocks and boulders, Douglas fir, spruce-fir, and aspen forests.
Elevation 1400–3400 m. (4600–11200 ft.) 2600–3700 m. (8500–12100 ft.)
Distribution
from FNA
AZ; CA; ID; MT; NV; OR; UT; AB
[WildflowerSearch map]
from FNA
CO
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 gemmipara is known only from Grand, Jefferson, Larimer, and Park counties in north-central Colorado. Flowers in this species are uncommon, and seed set has not been observed in natural populations; reproduction in nature appears to be solely asexual via overwintering propagules (bulbils) formed in leaf axils. Two meristems are initiated in each axil. The proximal meristem produces a pair of starch-thickened storage leaves, a rudimentary axis, and a distal pair of preformed leaf primordia that enclose the shoot apical meristem. Root primordia are present within the first node of the bulbil. The petiole of the subtending leaf expands laterally and folds adaxially to enclose the developing bulbil, and entangled trichomes along the petiole margins secure it following leaf abscission and dispersal. The leaf blades commonly are deciduous, leaving the bulbil still attached (M. R. Beardsley 1997).

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

Source FNA vol. 17, p. 408. FNA vol. 17, p. 395.
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. 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, E. willisii
Synonyms Mimulus tilingii, M. caespitosus var. implexus, M. implexus, M. implicatus, M. langsdorffii var. tilingii, M. lucens, M. veronicifolius Mimulus gemmiparus
Name authority (Regel) G. L. Nesom: Phytoneuron 2012-39: 44. (2012) (W. A. Weber) G. L. Nesom & N. S. Fraga: Phytoneuron 2012-39: 37. (2012)
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