The green links below add additional plants to the comparison table. Blue links lead to other Web sites.
enable glossary links

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

Charleston Mountains monkeyflower

Habit Perennials, rhizomatous, solitary to weakly colonial, rhizomes forming a mass, yellowish, branching, filiform. Annuals, fibrous-rooted, usually dark purplish.
Stems

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

erect, simple, weakly 4-angled, 4–16(–24) cm, slender, glabrous or sparsely villous-glandular near nodes.

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, basal usually persistent, largest at mid stem or above, cauline relatively few on long internodes;

petiole: proximals to distals 1–4 mm;

blade palmately 3-veined, ovate to ovate-lanceolate, 5–16(–20) × 3–11 mm, base truncate to subcordate, margins shallowly, evenly crenulate to serrate-dentate or denticulate, apex acute to obtuse, surfaces: proximals glabrous or sparsely villous, distals and bracteals sparsely hirtellous or glabrous abaxially or along distal margin, sparsely villous adaxially, hairs vitreous, flattened, eglandular.

Flowers

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

plesiogamous, (1–)4–7, usually from all nodes, usually beginning about mid stem, cleistogamous.

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, sparsely red-dotted, bilaterally or nearly radially symmetric, bilabiate or nearly regular;

tube-throat narrowly cylindric, 4–6 mm, exserted 0.5–1 mm beyond calyx margin;

limb barely expanded.

Fruiting pedicels

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

deflexed 45–90º at calyx, 6–19 mm, longer than subtending leaves, glabrous or sparsely villous-glandular.

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.

sometimes purple-dotted, broadly elliptic-ovoid, inflated, sagittally compressed, 10–13 mm, minutely hirtellous, sometimes also sparsely glandular, throat closing, adaxial lobe not distinctly longer than abaxial, not falcate.

Capsules

included, 5–7 mm.

included, stipitate, 6–8 mm.

Anthers

included, glabrous.

included, glabrous.

2n

= 28, 56.

Erythranthe tilingii

Erythranthe charlestonensis

Phenology Flowering Jul–Sep. Flowering Apr–Jul(–Aug).
Habitat Seeps, springs, stream banks, shallow rivulets, cliff bases, ledges and crevices, steep gravelly slopes, wet meadows. Grassy slopes, damp soils, moist rocks.
Elevation 1400–3400 m. (4600–11200 ft.) (900–)1700–2400(–2800) m. ((3000–)5600–7900(–9200) ft.)
Distribution
from FNA
AZ; CA; ID; MT; NV; OR; UT; AB
[WildflowerSearch map]
from FNA
AZ; NV
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 charlestonensis is characterized by its annual duration, autogamous reproduction, small stature, commonly purplish color, regularly ovate, short-petiolate leaves with shallowly crenate margins and (distal leaves) sparsely villous or glabrous adaxial surfaces, hirtellous calyces without a prominently longer adaxial lobe, and lack of glandular hairs. It is endemic to the Charleston (Spring) Mountains of Clark County, Nevada, and one locality (Union Pass) in Mohave County, Arizona.

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

Source FNA vol. 17, p. 408. FNA vol. 17, p. 423.
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. 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, E. willisii
Synonyms Mimulus tilingii, M. caespitosus var. implexus, M. implexus, M. implicatus, M. langsdorffii var. tilingii, M. lucens, M. veronicifolius
Name authority (Regel) G. L. Nesom: Phytoneuron 2012-39: 44. (2012) G. L. Nesom: Phytoneuron 2012-40: 80. (2012)
Web links