Erythranthe breviflora |
Erythranthe regni |
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short-flower monkey-flower |
King of Arizona monkeyflower |
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Habit | Annuals, shallowly fibrous-rooted. | Annuals, fibrous-rooted, sometimes rooting at proximal nodes. |
Stems | ascending, geniculate at nodes, branched at proximal and medial nodes, 4–15 cm, minutely stipitate-glandular, hairs 0.1–0.3 mm, gland-tipped, sometimes minutely hirtellous, hairs sharp-pointed, eglandular. |
erect to ascending-erect, branched, sometimes becoming slightly fistulose, 15–45 cm, glabrous. |
Leaves | usually cauline, basal usually deciduous by flowering; petiole 1–3 mm; blade palmately 3-veined, narrowly ovate or narrowly lanceolate to elliptic or elliptic-lanceolate, largest 5–15 × 2–6 mm, relatively even-sized, or slightly reduced distally, base attenuate, margins entire, mucronulate, or denticulate, apex acute to obtuse, surfaces minutely stipitate-glandular, hairs 0.1–0.3 mm, gland-tipped, sometimes minutely hirtellous, hairs sharp-pointed, eglandular. |
basal and cauline; petiole: proximals 5–25(–30) mm, mid cauline and distals not connate, 0 mm; blade palmately 5–7-veined, proximal sometimes subpinnate, proximals ovate to depressed-orbicular, 15–20(–50) × 15–25(–50) mm, medials and distals broadly depressed-ovate to obtriangular or flabellate, 15–35 mm, largest basal or at mid stem with distal slightly reduced, base attenuate-cuneate, margins shallowly serrate-dentate, sometimes irregularly, to mucronulate or apiculate, teeth (3–)5–7 per side, rarely subentire, apex rounded, surfaces glabrous. |
Flowers | plesiogamous, 10–20, from medial to distal nodes. |
plesiogamous, 6–16, from all nodes or medial to distal, cleistogamous. |
Styles | glabrous. |
glabrous. |
Corollas | yellow, red-spotted or striped, bilaterally symmetric, weakly bilabiate; tube-throat cylindric to narrowly funnelform, 3.5–5 mm, not exserted beyond calyx margin; limb barely widened, lobes broadly obovate, apex rounded. |
yellow, not red-dotted, bilaterally or radially symmetric, bilabiate or regular; tube-throat cylindric-funnelform, 9–12 mm, exserted 3–5 mm beyond calyx margin; limb expanded 1–1.5 mm. |
Fruiting pedicels | straight, 5–11 mm, minutely stipitate-glandular, hairs 0.1–0.3 mm, gland-tipped, sometimes minutely hirtellous, hairs sharp-pointed, eglandular. |
15–30 mm, longer than subtending leaves, glabrous. |
Fruiting calyces | winged, plicate-angled, campanulate becoming ovoid-ellipsoid to campanulate, distinctly inflated, 5–6 mm, margins distinctly toothed or lobed, sparsely, minutely hirtellous, eglandular, sometimes sparsely sessile-glandular, lobes pronounced, erect. |
sparsely purple-dotted, broadly campanulate-cylindric, inflated, sagittally compressed, 7–9 mm, glabrous, throat not closing, adaxial lobe longest. |
Capsules | included, 4–6 mm. |
included, 4–5 mm. |
Anthers | included, glabrous. |
included, glabrous. |
Erythranthe breviflora |
Erythranthe regni |
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Phenology | Flowering May–Jul. | Flowering Mar–May. |
Habitat | Stream and lake sides, gravel bars, springs, moist slopes, damp swales between dunes, along trails. | Moist to wet, sandy loam soils. |
Elevation | 700–2300 m. (2300–7500 ft.) | 800–1000 m. (2600–3300 ft.) |
Distribution |
CA; ID; MT; NV; OR; WA; BC
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AZ |
Discussion | Erythranthe regni is endemic to the Kofa Mountains of Yuma County; all collections have been made from the Kofa Game Refuge (Kofa National Wildlife Refuge). Because its calyces remain open at maturity, this species is hypothesized to be most closely related to E. geyeri, from which it differs by its erect habit, apparently annual duration, larger leaves, purple-dotted calyces, and corollas with longer tube-throat and barely bilabiate limb. Geography and other morphology, however, suggest that its evolutionary origins are closer to E. guttata. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Source | FNA vol. 17, p. 399. | FNA vol. 17, p. 406. |
Parent taxa | Phrymaceae > Erythranthe | Phrymaceae > Erythranthe |
Sibling taxa | ||
Synonyms | Mimulus breviflorus | |
Name authority | (Piper) G. L. Nesom: Phytoneuron 2012-39: 38. (2012) | G. L. Nesom: Phytoneuron 2012-40: 24. (2012) |
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