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bent-stem monkeyflower, Dudley's monkeyflower

Arizona big red monkeyflower

Habit Annuals, fibrous-rooted or filiform-taprooted. Perennials, rhizomatous.
Stems

ascending to decumbent or prostrate, geniculate at nodes, simple or diffusely branched, 5–60 cm, moderately villous, hairs 0.8–2 mm, multicellular, eglandular and also 0.1–0.3 mm, stipitate-glandular.

usually erect to ascending, freely branched, 25–60 cm, glabrous.

Leaves

basal and cauline, basal usually deciduous by flowering;

petiole 2–10(–35) mm;

blade pinnately to subpinnately veined, broadly ovate or elliptic-ovate to triangular, 8–35 × 5–30 mm, base cuneate to rounded or subcordate, margins serrate or dentate, teeth 3–10 per side, apex acute to obtuse or rounded, surfaces moderately villous, hairs 0.8–2 mm, multicellular, eglandular, and 0.1–0.3 mm, stipitate-glandular.

usually cauline;

petiole 0 mm;

blade palmately veined, elliptic to oblong-elliptic, elliptic-lanceolate, or broadly lanceolate, 60–125 × 25–46 mm, base narrowly auriculate, clasping to subclasping, margins shallowly dentate, teeth sharp-pointed, apex acute, adaxial surface glabrous or minutely sessile- or stipitate-glandular along veins, lamina glabrous.

Flowers

herkogamous, (1–)6–20, from all or medial to distal nodes.

herkogamous, 2–4(–8), axillary at leafy distal nodes.

Styles

glabrous.

glabrous.

Corollas

yellow, without white patches, throat red-spotted, spots concentrated or becoming coalescent into a somewhat discrete splotch at base of each of 3 abaxial lobes and sometimes 2 adaxial, bilaterally symmetric, ± bilabiate;

tube-throat cylindric, 9–12 mm, exserted beyond calyx margin;

limb expanded 10–18 mm diam.

deep orange, dull orange, red-orange, or deep scarlet, throat yellow-orange, dark red stripes leading onto basal part of lobes, not spotted, palate ridges red, bilaterally symmetric, strongly bilabiate;

tube-throat tubular, 29–36 mm, exserted 7–12 mm beyond calyx margin;

throat open, palate ridges densely short-villous, hairs yellowish.

Fruiting pedicels

12–26(–55) mm, moderately villous, hairs 0.8–2 mm, multicellular, eglandular and also 0.1–0.3 mm, stipitate-glandular.

50–95 mm.

Fruiting calyces

red-spotted, campanulate-cylindric, weakly inflated, (5–)6–8 mm, margins distinctly toothed or lobed, sparsely to moderately villous-glandular, ribs shallowly wing-angled, lobes pronounced, erect to spreading or spreading-recurving.

cylindric-campanulate, not inflated, (27–)29–34 mm, minutely stipitate- or sessile-glandular, lobes 7–10 mm, ovate, apex abruptly attenuate to linear-caudate.

Capsules

included, 4–6(–7) mm.

included, 14–18 mm.

Anthers

included, glabrous.

exserted, white-villous, thecae spreading.

2n

= 32.

= 16.

Erythranthe geniculata

Erythranthe cinnabarina

Phenology Flowering (Mar–)Apr–Jul. Flowering Jun–Aug(–Sep).
Habitat Granite crevices, canyon slopes, talus, crevices in volcanic outcrops, edges of boulders, roadsides, damp sandy soils, sandy water edges, gravelly soils and creek bottoms. Canyons, ravines, streambeds and margins, riparian vegetation, mixed conifer forest.
Elevation 200–900(–1200) m. (700–3000(–3900) ft.) 2100–3300 m. (6900–10800 ft.)
Distribution
from FNA
CA
[WildflowerSearch map]
from FNA
AZ
Discussion

Erythranthe geniculata is known from an apparently disjunct cluster of populations in Butte, Sutter, and Yuba counties and then from Tuolumne and Stanislaus counties south to Kern County.

Erythranthe geniculata, compared to E. floribunda, has larger, chasmogamous, and allogamous flowers. The anther pairs of E. geniculata are at different levels, and the stigma is slightly above the adaxial anther pair; in E. floribunda both anther pairs and the stigma are at the same level.

Erythranthe arenaria, E. geniculata, and E. norrisii constitute a group of apparently closely related species within sect. Mimulosma endemic along the Sierra Nevada. All have ovate-petiolate leaves (only the basal ones are sometimes ovate in E. arenaria) with pinnate to subpinnate venation. The more widespread E. floribunda, which is part of the above group, also is similar, but all three endemics have larger corollas with the tube exserted at greater length beyond the calyx margin.

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

Erythranthe cinnabarina is similar to typical E. cardinalis in its spreading anther thecae, relatively short-exserted corolla tube, and its reflexing corolla lobes but distinct in its generally larger leaves with reduced vestiture, fewer flowers, larger calyx and corolla, apically caudate calyx lobes, and its separate geographical range.

Erythranthe cinnabarina occurs in Cochise County (Chiricahua Mountains), Graham County (Pinaleño Mountains), and Pima County (Santa Catalina Mountains). Erythranthe verbenacea, with which it sometimes has been confused, occurs at lower elevations (350–2600 m) and ranges over most of the state (Apache, Cochise, Coconino, Gila, Graham, La Paz, Maricopa, Mohave, Pima, Pinal, Santa Cruz, and Yavapai counties). Erythranthe cinnabarina apparently occurs alone (without E. verbenacea) in the Pinaleño Mountains and in the Chiricahua Mountains, but both species have been abundantly documented in the Santa Catalina Mountains, where they sometimes closely co-occur in areas of elevational overlap (for example, at Marshall Gulch, about 2500 m; at Bear Wallow Campground, about 2600 m).

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

Source FNA vol. 17, p. 404. FNA vol. 17, p. 393.
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. 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
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. 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 geniculatus, M. dudleyi, M. floribundus var. geniculatus
Name authority (Greene) G. L. Nesom: Phytoneuron 2012-39: 38. (2012) G. L. Nesom: Phytoneuron 2014-31: 16, figs. 16, 17. (2014)
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