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Shockley's evening-primrose

beeblossom, browneyes

Habit Herbs annual, glandular puberulent throughout, or glabrate and glaucous distally. Herbs,usually annual, sometimes perennial, rarely biennial, usually caulescent.
Stems

several, 10–100 cm.

ascending to erect, usually branched.

Leaves

primarily in poorly defined basal rosette, cauline greatly reduced when present;

petiole 0.4–8 cm;

blade unlobed, ovate to cordate, 2–11.5 × 1.4–5 cm, margins sinuate-dentate, brown oil cells prominently lining veins abaxially.

basal and cauline, cauline often reduced, basal often forming well-developed rosette, alternate;

stipules absent; long-petiolate;

blade often pinnately (rarely bipinnately) lobed, sometimes unlobed, or lateral lobes greatly reduced or absent, terminal lobe usually large, margins usually regularly or irregularly dentate to serrate, sometimes denticulate, serrulate, or entire, abaxial surface or margin with ± conspicuous, usually brown, oil cells.

Racemes

erect, elongating in anthesis.

Inflorescences

racemes, erect or nodding.

Flowers

opening at sunrise;

buds without free tips;

floral tube 2–5 mm, villous inside;

sepals 1.5–3.5 mm;

petals lavender, paler and often with flecks toward base, often yellow at very base, fading darker lavender, 2–6 mm;

stamens unequal, filaments of antisepalous ones 1.8–3 mm, of antipetalous ones 1–2.5 mm, anthers 0.6–1 mm, glabrous or sparsely ciliate;

style 4–7 mm, stigma surrounded by anthers at anthesis.

bisexual, actinomorphic, buds usually erect, sometimes reflexed;

floral tube deciduous (with sepals, petals, and stamens after anthesis), with basal nectary;

sepals 4, reflexed singly;

petals 4, usually yellow or white, often fading orange-red, sometimes lavender or purple, rarely cream, often with 1+ red dots near base;

stamens usually 8, in 2 subequal series, rarely 4 in 1 series (usually in C. exilis), anthers versatile, pollen shed singly or in tetrads;

ovary 4-locular, stigma usually entire and capitate, rarely conical-peltate and ± 4-lobed, surface unknown, probably wet and non-papillate.

Fruit

a capsule, straight or slightly curved, subterete and clavate or oblong-cylindrical, regularly loculicidal; pedicellate.

Capsules

erect, clavate, 7–13 mm;

pedicel 2–5 mm.

Seeds

1–1.2 mm.

numerous, in 2 rows per locule, lenticular to narrowly ovoid to narrowly obovoid, finely pitted, with ± pronounced membranous margin when immature.

xI> = 7.

2n

= 14.

Chylismia heterochroma

Chylismia

Phenology Flowering May–Jun.
Habitat Alluvial and rocky slopes.
Elevation 600–2200 m. (2000–7200 ft.)
Distribution
from FNA
CA; NV
[WildflowerSearch map]
[BONAP county map]
w United States; nw Mexico
[BONAP county map]
Discussion

Chylismia heterochroma is known from Churchill and Lander counties, Nevada, south to Lincoln and southern Nye counties, Nevada, to adjacent California (Mono Lake, Mono County, and central Inyo counties). P. H. Raven (1962, 1969) determined this species to be self-compatible and autogamous.

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

Species 16 (16 in the flora).

Chylismia is distinguished from other genera formerly included in Camissonia by straight to arcuate (never twisted or curled) capsules on distinct pedicels and seeds in 2 rows per locule. R. A. Levin et al. (2004) included only one species each from Camissonia sects. Chylismia and Lignothera; the two formed a moderately supported branch, which led W. L. Wagner et al. (2007) to recognize Chylismia as a distinct genus. Chylismia is strongly supported in a sister relationship to the realigned Oenothera. This clade is in turn sister to Eulobus. Reproductive features include: self-incompatible (C. brevipes, C. claviformis, C. multijuga, C. munzii, and probably C. confertiflora, C. eastwoodiae, and C. parryi; P. H. Raven 1962, 1969) or self-compatible; flowers diurnal, outcrossing and pollinated by mostly oligolectic bees or autogamous, or opening one to two hours before sunset (in one subspecies of C. claviformis and the two species of sect. Lignothera); the evening-opening subspecies of C. claviformis pollinated mostly by oligolectic bees and moths, C. cardiophylla mainly by small moths, and C. arenaria, with its long floral tubes, by hawkmoths (E. G. Linsley et al. 1963, 1963b, 1964). Most species are diploid (2n = 14) but there are occasional tetraploids (2n = 28); floating translocations are relatively common (Raven 1962, 1969).

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

Key
1. Floral tubes 0.4–9 mm; pollen shed singly; leaves basal and cauline, usually with well-developed basal rosettes, blades usually pinnately or bipinnately lobed, lateral lobes sometimes greatly reduced or absent; plants usually annual, sometimes perennial, rarely biennial.
sect. Chylismia
1. Floral tubes 4.5–40 mm; pollen shed in tetrads; leaves cauline, blades unlobed; plants usually perennial, sometimes annual.
sect. Lignothera
Source FNA vol. 10. FNA vol. 10. Author: Warren L. Wagner.
Parent taxa Onagraceae > subfam. Onagroideae > tribe Onagreae > Chylismia > sect. Chylismia Onagraceae > subfam. Onagroideae > tribe Onagreae
Sibling taxa
C. arenaria, C. atwoodii, C. brevipes, C. cardiophylla, C. claviformis, C. confertiflora, C. eastwoodiae, C. exilis, C. megalantha, C. multijuga, C. munzii, C. parryi, C. scapoidea, C. specicola, C. walkeri
Subordinate taxa
C. sect. Chylismia, C. sect. Lignothera
Synonyms Oenothera heterochromas., Camissonia heterochroma, C. heterochroma var. monoensis, O. heterochroma subsp. monoensis, O. heterochroma var. monoensis Oenothera, Camissonia section chylismia, Oenothera section chylismia, Oenothera subg. chylismia
Name authority (S. Watson) Small: Bull. Torrey Bot. Club 23: 193. (1896) — (as Chylisma) (Torrey & A. Gray) Nuttall ex Raimann in H. G. A. Engler and K. Prantl: Nat. Pflanzenfam. 96[III,7]: 217. (1893)
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