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tinytooter monkeyflower

Hall's monkeyflower

Habit Annuals, fibrous-rooted, sometimes producing leafy runners from basal nodes, stems often rooting at proximal nodes and appearing rhizomelike. Annuals, fibrous-rooted, sometimes apparently rooting at proximal nodes if stems proximally decumbent.
Stems

usually erect, usually simple, usually fistulose, 12–40(–100) cm, sparsely stipitate-glandular, hairs fine, gland-tipped.

erect, simple, 4-angled, 2–8 cm, slender, glabrous.

Leaves

basal and cauline, basal persistent;

petiole: basal and proximals 6–20(–40) mm, midcauline to distals 0 mm;

blade not connate, palmately 3–5(–7)-veined, orbicular to broadly elliptic-ovate or oblong-elliptic, cauline becoming broadly ovate to narrowly reniform, basal and mid cauline 15–30(–50) mm, gradually reduced in size distally to 6 mm, basal largest, distal closely paired, auriculate-subclasping, base cuneate to truncate or shallowly cordate, margins shallowly, evenly to unevenly dentate, apex obtuse to rounded, surfaces glabrous.

basal and cauline or basal deciduous, largest at mid stem or above, cauline relatively few on long internodes;

petiole: basal and proximals to midcauline 1–4 mm, distals 0 mm;

blade palmately 3-veined, ovate to ovate-lanceolate, 5–11 × 3–9 mm, base truncate to cuneate, margins very shallowly dentate or denticulate, apex acute to obtuse, surfaces glabrous or distals and bracteals sparsely villous, hairs vitreous, flattened, eglandular, multicellular.

Flowers

plesiogamous, (5–)10–16, at distal nodes, in bracteate racemes, chasmogamous or cleistogamous.

plesiogamous, (1–)4–10, sometimes from all nodes, usually beginning about mid stem, cleistogamous.

Styles

glabrous.

glabrous.

Corollas

yellow, red-spotted, abaxial limb deeper yellow, weakly bilaterally or radially symmetric, weakly bilabiate or regular;

tube-throat sometimes tubular and not opening (cleistogamous), 8–14 mm, exserted 1–3 mm beyond calyx margin;

limb not expanded or expanded 9–14 mm.

yellow, usually red-dotted, bilaterally or nearly radially symmetric, bilabiate or nearly regular;

tube-throat narrowly cylindric, 4–6 mm, exserted 0.5–1 mm beyond calyx margin;

limb barely expanded.

Fruiting pedicels

10–30(–45) mm, longer than subtending leaves, minutely stipitate-glandular.

usually deflexed 90º at calyx, 6–14 mm, longer than subtending leaves.

Fruiting calyces

nodding 45–90º, not red-dotted, broadly elliptic-ovoid, inflated, sagittally compressed, (8–)14–18(–20) mm, glabrous or sparsely stipitate-glandular to hirsutulous, sometimes mixed glandular-hirsutulous, throat closing, adaxial lobe not distinctly longer than abaxial, not falcate.

sometimes red-dotted, broadly elliptic-ovoid, inflated, sagittally compressed, (5–)7–10 mm, glabrous, throat closing, adaxial lobe not distinctly longer than abaxial, not falcate.

Capsules

included, stipitate, 5–7 mm.

included, 4–6 mm.

Anthers

included, glabrous.

included, glabrous.

2n

= 60.

= 32.

Erythranthe cordata

Erythranthe hallii

Phenology Flowering (Jan–)Mar–Jun(–Nov). Flowering May–Aug.
Habitat Springs, seeps, stream edges, muddy banks, flood plains, marshes and swamps, wash bottoms, wet depressions, wet places among boulders. Ledges, seeps, along streams, wet meadows.
Elevation (600–)800–2400(–3000) m. ((2000–)2600–7900(–9800) ft.) 1900–3200 m. (6200–10500 ft.)
Distribution
from FNA
AZ; CA; CO; NM; NV; TX; UT
[WildflowerSearch map]
from FNA
CO
Discussion

Erythranthe cordata is characterized by its fibrous-rooted habit (annual in duration, without rhizomes but commonly rooting at the proximal nodes), short corollas and autogamous reproduction (anthers and stigma at the same level), closed calyces, sparsely villous-glandular vestiture (lacking hirtellous, eglandular hairs), and stems commonly fistulose in larger plants. The short corollas and other features of autogamous reproduction of E. cordata are diagnostic and prominent. Plants of E. cordata are highly variable in size, from tiny fibrous-rooted plants with nearly filiform stems to much larger individuals with fistulose stems rooting at proximal nodes.

Erythranthe cordata and E. nasuta are sympatric in Arizona, southeastern New Mexico, and southern Utah, and small plants of each species may be similar in aspect, both with cleistogamous flowers and reduced vestiture. Erythranthe nasuta can be recognized by its distal and bracteal leaves with hirtellous to hirsutulous adaxial surfaces; a 10/x lens usually is required to see this feature, and it sometimes is most obvious around the leaf margins.

The common name of Erythranthe cordata alludes to a fancied resemblance of the corollas to the horn of a diminutive trumpet.

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

Erythranthe hallii is known from Boulder, Clear Creek, Fremont, Grand, Jefferson, Larimer, Routt, and Saguache counties. The Colorado population system is morphologically and geographically coherent.

Erythranthe hallii is similar to E. arvensis; both have four-angled stems, autogamous reproduction, a tendency to root at basal nodes and distally, and both have bracteal leaves villous with vitreous, flattened, eglandular, multicellular hairs, although this vestiture is barely developed and often absent in E. hallii. The only reported chromosome number from the Colorado plants (2n = 32) also appears to be distinct among possible relatives of E. hallii.

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

Source FNA vol. 17, p. 422. FNA vol. 17, p. 423.
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. 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
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. 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 cordatus, M. maguirei Mimulus hallii, M. guttatus var. hallii
Name authority (Greene) G. L. Nesom: Phytoneuron 2012-39: 43. (2012) (Greene) G. L. Nesom: Phytoneuron 2012-39: 43. (2012)
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