Erythranthe rubella |
Erythranthe laciniata |
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little redstem monkeyflower, red stem himulus, redstem monkeyflower, redstem or little redstem monkeyflower |
cut-leaf monkeyflower |
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Habit | Annuals, taprooted. | Annuals, slender-taprooted or fibrous-rooted. |
Stems | erect, simple, sometimes branched from basal nodes, 3–32 cm, minutely puberulent. |
erect, simple or branched from base, 3–38 cm, glabrous or sparsely hirtellous, finely villosulous-glandular above nodes. |
Leaves | cauline, basal not persistent; petiole 0 mm; blade palmately 3-veined (in broader ones), linear to elliptic, 5–22(–30) × 1–5 mm, base narrowed, margins entire, sometimes toothed, apex acute to obtuse, surfaces minutely puberulent. |
cauline, basal deciduous by flowering; petiole 1–35 mm, distals 0 mm; blade 1-veined or palmately 3-veined, elliptic to elliptic-obovate, oblanceolate, or oblong, 3–55 mm, longer than wide, base attenuate, margins narrowly pinnately lobed or dissected, sometimes merely shallowly toothed, apex acute to obtuse, surfaces glabrate. |
Flowers | herkogamous, sometimes plesiogamous, 1–106, from distal or medial to distal nodes. |
plesiogamous, 2–8, from medial to distal nodes, chasmogamous, sometimes cleistogamous. |
Styles | glabrous. |
glabrous. |
Corollas | yellow and abaxial limb and throat red dotted or pink to purple and throat yellow, bilaterally symmetric, weakly bilabiate; tube-throat cylindric, 4–10 mm, exserted beyond calyx margin; limb expanded 3–5 mm, lobes entire or weakly notched, abaxial limb glabrous. |
yellow, throat red-spotted, abaxial limb of larger usually with 1 large red splotch, bilaterally symmetric, ± bilabiate; tube-throat funnelform, 4–6 mm, exserted 1–2 mm beyond calyx margin; limb expanded 5–6 mm. |
Fruiting pedicels | 2–18 mm. |
nodding 30–140º at calyx base, 5–25 mm. |
Fruiting calyces | becoming red-angled or red, campanulate to nearly cylindric, 4–9 mm, margins distinctly toothed or lobed, glabrous or minutely puberulent, ribs thickened, lobes pronounced, erect, margins ciliate. |
red-spotted, cylindric-campanulate, inflated, sagittally compressed, 8–10 mm, glabrate, throat closing, lobes ca. equal size or adaxial slightly longer. |
Capsules | included, 3–8 mm. |
included, stipitate, 5–7 mm. |
Anthers | included, glabrous. |
included, glabrous. |
2n | = 28. |
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Erythranthe rubella |
Erythranthe laciniata |
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Phenology | Flowering Apr–Jun. | Flowering Apr–Jul(–Aug). |
Habitat | Open slopes and washes. | Cracks, depressions, and seeps in granite outcrops, ledges, talus and scree, rocky streamsides, rocky slopes, roadsides, intermittent drainages. |
Elevation | 300–3000 m. [1000–9800 ft.] | 900–2300(–3300) m. [3000–7500(–10800) ft.] |
Distribution |
AZ; CA; CO; NM; NV; TX; UT; WY; Mexico (Baja California, Sonora)
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CA
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Discussion | Erythranthe laciniata is known from Amador County south to Kern County. As in Erythranthe nasuta, the adaxial calyx lobe in E. laciniata tends to be narrowly lanceolate to triangular (noselike) and perceptibly falcate, curving slightly upward both in flower and in fruit. The adaxial lobe is not so prominently protruding as it often is in E. nasuta. Corolla size is variable in Erythranthe laciniata, but the size of those with an open throat (versus much reduced in size and apparently cleistogamous) is not strongly correlated with size of the individual plant, and all on one plant are about the same size (compare with E. nasuta). Corollas on some plants, however, are all or nearly all greatly reduced and apparently cleistogamous. Fertilization in even the larger corollas apparently is autogamous; the anther pairs are slightly separated or equal in level, and the stigma is in the middle of the anthers or at the level of the adaxial pair. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 17, p. 384. | FNA vol. 17, p. 419. |
Parent taxa | ||
Sibling taxa | ||
Synonyms | Mimulus rubellus, M. gratioloides | Mimulus laciniatus, M. eisenii |
Name authority | (A. Gray) N. S. Fraga: Phytoneuron 2012-39: 35. (2012) | (A. Gray) G. L. Nesom: Phytoneuron 2012-39: 44. (2012) |
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