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Cypripedium californicum

California lady slipper, California lady's-slipper

ivory lady's-slipper, Kentucky lady's slipper, purloined slipper, southern lady's slipper

Habit Plants erect, 25–120 cm. Plants erect, 35–97 cm.
Leaves

5–10, along length of stem, alternate, ascending to spreading;

blade elliptic-lanceolate to broadly elliptic, 5–16 × 1.5–6.5 cm.

3–6, rather evenly spaced along stem, alternate, spreading;

blade broadly ovate to ovate-lanceolate or ovate-elliptic, 13–24 × 4.3–15 cm.

Flowers

3–18(–22);

sepals yellow-green to pale brownish yellow;

dorsal sepal elliptic, 14–20 × 7–13 mm;

lateral sepals connate almost to apex;

synsepal 12–20 × 10–12 mm;

petals spreading, same color as sepals or more yellowish, linear-oblong to linear-lanceolate, flat, 14–16 × 3–5 mm;

lip white, sometimes pinkish, obovoid, 15–20 mm;

orifice basal, 11–14 mm;

staminode suborbicular-subauriform.

1–2;

sepals greenish or yellowish, heavily spotted, striped, reticulately marked with dark reddish brown or madder;

dorsal sepal broadly ovate to ovate and elliptic, 61–126 × 24–65 mm;

lateral sepals connate;

synsepal 55–103 × 12–40 mm;

petals spreading-deflexed, same color as sepals, spirally twisted, linear, 84–156 × 7–15 mm;

lip ivory to pale yellow, obovoid, (41–)53–65 mm;

orifice basal, 27–37 mm;

staminode broadly ovoid, ovoid-cordiform, or ovoid-deltoid.

Cypripedium californicum

Cypripedium kentuckiense

Phenology Flowering May–Jun. Flowering Apr–Jun.
Habitat Forest openings, especially on steep slopes, in seeps, springy marshes Rich, mesic to dry, deciduous forests on well-drained alluvium and bases of slopes, mucky seeps
Elevation 0–1600 m (0–5200 ft) mostly 0–400 m (mostly 0–1300 ft)
Distribution
from FNA
CA; OR
[WildflowerSearch map]
[BONAP county map]
from FNA
AL; AR; GA; KY; LA; MS; OK; TN; TX; VA
[WildflowerSearch map]
[BONAP county map]
Discussion

The brief nomenclatural history of Cypripedium kentuckiense is remarkably confused. The plant was originally described, without Latin diagnosis, as C. daultonii Soukup; this nomen nudum came into general usage prior to Reed’s publication. Subsequently, an earlier name, C. furcatum Rafinesque, was proposed as conspecific, but Rafinesque’s description is not adequate for a positive determination.

Cypripedium kentuckiense is very distinctive. In addition to the very large flowers and pale coloring of the lip, the form of the orifice is unique. In related species the orifice is a restricted opening in the adaxial surface of the lip; in C. kentuckiense the orifice replaces the basal portion of the adaxial surface, the sides of the lip terminating abruptly at the orifice without curving toward the horizontal. In herbarium specimens this detail is obscured, but the cavernous nature of the orifice is emphasized by the adaxial surface descending from the apical margin of the orifice toward the apex of the lip; the obovoid lip appears to hang from the margin of the orifice, and the lip is not particularly slipper-shaped. In contrast, in related species, the adaxial surface of the lip surrounds the orifice and extends forward toward the apex, forming a more convincing slipper. These distinctions hold virtually throughout the known populations of C. kentuckiense; only in two Arkansas populations is the lip form suggestive of related species. The Arkansas populations may reflect very limited introgression from C. parviflorum var. pubescens.

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

Source FNA vol. 26, p. 503. FNA vol. 26, p. 506.
Parent taxa Orchidaceae > subfam. Cypripedioideae > Cypripedium Orchidaceae > subfam. Cypripedioideae > Cypripedium
Sibling taxa
C. acaule, C. arietinum, C. candidum, C. fasciculatum, C. guttatum, C. kentuckiense, C. montanum, C. parviflorum, C. passerinum, C. reginae, C. yatabeanum
C. acaule, C. arietinum, C. californicum, C. candidum, C. fasciculatum, C. guttatum, C. montanum, C. parviflorum, C. passerinum, C. reginae, C. yatabeanum
Name authority A. Gray: Proc. Amer. Acad. Arts 7: 389. (1868) C. F. Reed: Phytologia 48: 426, fig. (1981)
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