Erythranthe microphylla |
Erythranthe carsonensis |
|
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Bentham's monkeyflower, small-leaf monkey-flower |
Carson Valley monkeyflower |
|
Habit | Annuals, fibrous-rooted. | Annuals, taprooted, densely compact. |
Stems | erect, simple, sometimes many-branched from basal cauline nodes, terete, sometimes distinctly 4-angled, (3–)5–30(–45) cm, glabrous below inflorescence, sometimes distals hirtellous, hairs commonly deflexed, or mixed hirtellous and stipitate-glandular, sometimes only short villous-glandular, hairs gland-tipped. |
erect, simple or branched from basal nodes, 2–7(–8) cm, minutely glandular, internodes shortened, not evident. |
Leaves | basal and cauline, basal sometimes absent at flowering; petiole: basal or proximals to medials 3–25(–35) mm, distals 0 mm (then blade subclasping to narrowly perfoliate); blade often purplish, palmately 3–5-veined, ovate or ovate-lanceolate to elliptic-ovate, suborbicular, or depressed-ovate, (3–)10–35 × 3–25 mm, base rounded to truncate or subcordate, margins shallowly crenate to sharply crenate-serrate, teeth 5–10 per side, basal and proximal often irregularly incised near petiole and sublyrate, apex acute to obtuse-rounded, surfaces glabrous or sparsely to moderately hirtellous, eglandular. |
cauline, basal not persistent; petiole 0 mm; blade palmately 3-veined (in broader ones), linear to spatulate, (3–)5–23 × 1–5 mm, base truncate to truncate-cordate, clasping, margins entire, apex acute to obtuse, surfaces minutely glandular. |
Flowers | herkogamous, 1–8(–14), usually from distal nodes, chasmogamous. |
herkogamous, 1–35, from distal or medial to distal nodes. |
Styles | sparsely hirtellous. |
glabrous. |
Corollas | yellow to golden yellow or orangish yellow, usually red-spotted, abaxial limb sometimes with a large red splotch, bilaterally symmetric, bilabiate; tube-throat broadly funnelform, (6–)8–16(–20) mm, exserted (1–)2–6(–8) mm beyond calyx margin; limb expanded 8–25 mm, palate villous. |
yellow, palate red-dotted and 1 large central spot, bilaterally symmetric, strongly bilabiate; tube-throat cylindric, distinct from abruptly expanding throat, (5–)7–11 mm, exserted beyond calyx margin; limb expanded 7–12(–15) mm, each lobe 2-fid, palate densely bearded. |
Fruiting pedicels | 8–30(–50) mm, distals hirtellous, hairs commonly deflexed, or mixed hirtellous and stipitate-glandular, sometimes only short villous-glandular, hairs gland-tipped. |
(3–)5–14 mm. |
Fruiting calyces | nodding 30–90º, sometimes red-tinged or -dotted, ovoid-campanulate to broadly cylindric-campanulate, inflated, sagittally compressed, (7–)9–16(–20) mm, minutely hirtellous, hairs sometimes reduced to basal cells, or glabrous, throat strongly to weakly closing. |
campanulate to widely urceolate, 4–7 mm, margins distinctly toothed or lobed, minutely glandular, ribs thickened, lobes pronounced, erect. |
Capsules | included, 6–9(–11) mm. |
included, 3–6 mm. |
Anthers | included, glabrous. |
included, glabrous. |
2n | = 28, 56. |
|
Erythranthe microphylla |
Erythranthe carsonensis |
|
Phenology | Flowering Mar–Jul. | Flowering Mar–Jun. |
Habitat | Rock depressions, rocky ridges, cliff faces, roadcuts, wet meadows, seeps, stream banks, drying ponds, ephemeral stream channels, vernal springs over serpentine, roadsides and roadside ditches, dry banks, lava soils, loam, clay, gravel, yellow pine, oak-pine, mixed oak woodlands, oak-chaparral. | Openings in sage brush/bitterbrush scrub in sand of decomposed granite. |
Elevation | 20–1700(–2600) m. (100–5600(–8500) ft.) | 1400–1800 m. (4600–5900 ft.) |
Distribution |
CA; ID; NV; OR; WA; BC
|
CA; NV |
Discussion | Erythranthe microphylla is characterized by its annual duration (fibrous-rooted), usually simple stems, relatively widely spaced leaves, glabrous or hirtellous vestiture, open corollas, and calyces closing at the throat. Even in the smallest corollas, the stigma is positioned above the adaxial anther pair, indicating that all are primarily allogamous. Some plants have basal and proximal cauline leaves with exaggeratedly and irregularly toothed-incised margins (especially in Lake and Napa counties, California, as in the types of Mimulus glareosus and M. guttatus var. insignis, respectively), but a similar tendency can be seen over most of the geographic range. Plants of E. microphylla vary greatly in height, leaf size, and flower size (the larger flowers approaching the size of those in E. grandis and E. decora), yet all seem to be within the expression of a single species. An inversion sequence of chromosome 8 (the DIV1 region) is perfectly correlated with the life history features of at least four species of sect. Simiolus (D. B. Lowry and J. H. Willis 2010). One sequence occurs in Erythranthe guttata and E. grandis, which are perennial and rhizomatous, occur in habitats with year-round moisture, and flower relatively late in the season, while the opposite sequence occurs in E. nasuta and E. microphylla, which are annual and slender-taprooted or fibrous-rooted, occur in quickly drying habitats, and flower in early season. The inversion, with its tightly linked, locally adaptive alleles, contributes to isolating mechanisms between species with contrasting sequences and preserves the constellation of features that makes each a recognizable entity. Hybridization and apparent introgression occur among Erythranthe guttata, E. microphylla, and E. nasuta, yet each remains distinct in duration, perennating morphology, and habit. Erythranthe arvensis (annual) also is a member of this gene-sharing group. A whole-genome analysis by A. D. Twyford and J. Friedman (2015) showed that populations of E. guttata and E. microphylla cluster together within each of several geographically delimited regions; they interpreted their trees as showing phylogenetic relationships and concluded that E. guttata and E. microphylla are conspecific. Other evidence (G. L. Nesom 2014c, 2014d), particularly the DIV1 inversion sequence, indicates that E. guttata and E. grandis are most closely related to each other and were derived from an ancestor of annual duration. Thus, E. microphylla and E. nasuta are morphologically and phylogenetically distinct from E. guttata, despite extensive gene flow where they are sympatric with it. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Erythranthe carsonensis is restricted to the Carson Valley, Eagle Valley, and Washoe Valley region of Nevada and adjacent California, with one known disjunct occurrence about 58 km to the north in Nevada. The species was previously included in the broader concept of E. montioides but can be distinguished by its much branched and compact habit, linear to spatulate leaves with clasping bases, calyx with glabrous margins, and larger corolla with one large red spot in the center. Erythranthe carsonensis has been impacted by agriculture, urbanization, and other anthropogenic changes. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 17, p. 415. | FNA vol. 17, p. 384. |
Parent taxa | Phrymaceae > Erythranthe | Phrymaceae > Erythranthe |
Sibling taxa | ||
Synonyms | Mimulus microphyllus, M. glareosus, M. guttatus var. depauperatus, M. guttatus var. insignis, M. guttatus var. microphyllus, M. guttatus var. platycalyx, M. langsdorffii var. insignis, M. langsdorffii var. microphyllus, M. luteus var. depauperatus, M. nasutus var. insignis, M. platycalyx | Mimulus rubellus var. latiflorus |
Name authority | (Bentham) G. L. Nesom: Phytoneuron 2012-39: 44. (2012) | N. S. Fraga: Aliso 30: 59, figs. 17–21. (2012) |
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