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primrose monkey-flower

Pennell's panther

Habit Perennials, rhizomatous or stoloniferous, mat-forming, rhizomes or stolons flagelliform. Annuals, fibrous-rooted or taprooted.
Stems

erect to ascending, usually simple, 2–10(–20) cm, villous, internodes shortened.

decumbent-ascending, erect distally, simple, sometimes branched from proximal to medial nodes, 5–30 cm, short, delicately stipitate-glandular, distals minutely puberulent-glandular, hairs 0.1–0.4 mm (to 1 mm on proximal portions of stems), gland-tipped.

Leaves

all basal or near basal, often rosulate;

petiole 0 mm;

blade palmately 3-veined, oblanceolate to elliptic-obovate, 7–40 × 4–12 mm, base cuneate to attenuate, margins entire, distally denticulate to dentate, or sharply serrate-dentate, apex acute to obtuse, abaxial surface glabrous, adaxial glabrous or glabrate to sparsely to densely long-villous, eglandular.

usually cauline, basal usually not persistent;

petiole: proximals and medials 8–20 mm, distalmost 1–2 mm;

blade palmately 3-veined, usually ovate or broadly ovate to depressed-ovate, proximals and medials 7–22 × 6–18 mm, sometimes largest at mid stem, base rounded or cuneate to gradually attenuate, margins shallowly dentate-serrate, teeth 2 or 3(–5) per side mostly distally, apex obtuse to obtuse-acuminate, surfaces sparsely villous to puberulent-glandular, hairs vitreous, gland-tipped, sometimes glabrous.

Flowers

herkogamous, 1.

plesiogamous, 2–12, usually evenly distributed from proximal to distal nodes, chasmogamous, anther pairs in larger corollas slightly separated, stigma at level of distal pair, or both anther pairs and stigma at same level; in smaller corollas without expanded limb and barely exserted beyond calyx margin, both anther pairs and stigma at same level.

Styles

glabrous.

glabrous.

Corollas

yellow to orange-yellow, usually brown-spotted abaxially, base of each abaxial lobe usually with a larger reddish brown spot, bilaterally or nearly radially symmetric, weakly bilabiate or nearly regular, densely hirsute on abaxial side of opening;

tube-throat narrowly campanulate, 15–20 mm, exserted beyond calyx margin;

lobes broadly obovate-oblong, apex rounded- or truncate-notched, throat open, palate densely villous, abaxial ridges prominent.

yellow, throat floor sometimes red-spotted, bilaterally symmetric, bilabiate;

tube-throat narrowly funnelform to cylindric, 7–10(–12) mm, exserted 1–3 mm beyond calyx margin;

limb expanded 8–12 mm, palate villous.

Fruiting pedicels

30–110(–130) mm, glabrous or sparsely stipitate-glandular near base.

10–35 mm, short, delicately stipitate-glandular, distals minutely puberulent-glandular, hairs 0.1–0.4 mm, gland-tipped.

Fruiting calyces

tubular-campanulate, weakly or not inflated, 6–8 mm, glabrous.

nodding 45–180º, consistently dark purple-spotted, cylindric-campanulate, inflated, sagittally compressed, 8–11 mm, glabrous or sparsely puberulent-glandular, sometimes minutely hirtellous, throat closing.

Capsules

included, 6–7 mm.

included, stipitate, 4–6 mm.

Anthers

slightly exserted, margins ciliate, glabrous.

included, glabrous.

2n

= 34.

= 28.

Erythranthe primuloides

Erythranthe pardalis

Phenology Flowering Jun–Aug. Flowering (Mar–)Apr–May.
Habitat Wet meadows, seeps, streamsides. Crevices of serpentine rock, stony red soils, red clay, among boulders, along streams, ditches, tailings at copper mines.
Elevation 600–3400 m. (2000–11200 ft.) 100–700 m. (300–2300 ft.)
Distribution
from FNA
AZ; CA; ID; MT; NM; NV; OR; UT; WA
[WildflowerSearch map]
from FNA
CA
Discussion

Flowers in Erythranthe primuloides and E. linearifolia characteristically appear to be scapose, but the scapes are pedicels arising from axils of greatly foreshortened stems. Occasionally in both species the internodes may lengthen somewhat, and the leaves are not so densely clustered at the base of the stems.

In northern Klamath, western Deschutes, and eastern Douglas counties, Oregon, an area within the range of typical populations, Erythranthe primuloides has distinctively large corollas (limbs 10–15 mm wide). Apparent clones of large-flowered and smaller-flowered plants sometimes grow in close proximity or even intermixed, appearing as two different entities.

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

The relative constancy of Erythranthe pardalis in morphology suggests that genetic influence from other species is slight. It is recognized by its annual duration and relatively delicate habit, ovate to depressed-ovate leaves toothed mostly on the distal margins, small flowers produced from all nodes (proximal to distal), dark-spotted calyces, and stipitate-glandular cauline and foliar vestiture. While the corolla limbs are distinctly expanded, the tubes are only slightly exserted from the calyx, and flowers apparently are plesiogamous. The epithet pardalis alludes to the dark-spotted calyx.

Plants of Erythranthe pardalis occur primarily on serpentine rocks and soils but also grow on copper tailings at mine sites. The species is known from Amador, Calaveras, El Dorado, Placer, Tehama, and Tuolumne counties. The plants in Tehama County, geographically and ecologically disjunct from the main range, were recorded as growing in basalt crevices.

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

Source FNA vol. 17, p. 389. FNA vol. 17, p. 420.
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. 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. 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 primuloides, M. nevadensis, M. pilosellus, M. primuloides var. minimus, M. primuloides var. pilosellus Mimulus pardalis, M. cupriphilus, M. guttatus var. cupriphilus, M. guttatus var. pardalis
Name authority (Bentham) G. L. Nesom & N. S. Fraga: Phytoneuron 2012-39: 35. (2012) (Pennell) G. L. Nesom: Phytoneuron 2012-39: 44. (2012)
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