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giant purple wakerobin, giant trillium, giant wakerobin, sessile trillium, small-flower trillium

small-flower trillium

Rhizomes

± erect, brownish, somewhat compressed-thickened, superficially bulblike, praemorse, not brittle.

horizontal to ± erect, brownish, thick, praemorse, not brittle.

Scapes

1–3, green, round in cross section, 2–6.5 dm, robust.

1–3, round in cross section, 1.7–3 dm, slender to robust, glabrous.

Bracts

held well above ground, sessile (narrowing of bract blade may give bract subsessile appearance);

blade densely to weakly mottled in dark brownish green, mottling becoming more obscure to absent as bract matures, broadly ovate, 7–17.6 × 7.4–17.7 cm, not glossy, apex obtuse-rounded.

held well above ground, sessile;

blade green with widely scattered mottling, mottling becoming obscure with age, ovate to broadly ovate, 6.5–16 × 5–8 cm, not glossy, apex obtuse.

Flower

erect, odor roselike, spicy;

sepals spreading-ascending above bracts, green, lanceolate, 35–65 × 7–12 mm, margins entire, flat, apex obtusely rounded;

petals long-lasting, erect, connivent, ± concealing stamens and ovary, yellow, bronze, maroon, brown, deep purple, reddish brown, pink, dark purplish red, purplish bronze, rarely greenish white, not spirally twisted, veins not engraved, oblanceolate to obovate, 6.5–10 × 1.5–2.5 cm, thick-textured, base cuneate, margins entire, apex variably acute to almost truncate, erose;

stamens erect, purplish, 17–26 mm;

filaments purple, ca. 4 mm, widest at base, much shorter than anther sacs;

anthers erect, straight, ± purple-brown, 13–22 mm, dehiscence introrse;

connectives purple, straight, extended ca. 1–1.5 mm beyond anther sacs;

ovary purple, ovoid, 6-angled, 6–12 mm;

stigmas small, divergent or erect, distinct, purple, subulate, 4–8 mm, not fleshy.

erect, odor spicy, of cloves;

sepals displayed above bracts, spreading, divergent, green, lanceolate, 16–25 × 4–8 mm, margins entire, flat, apex variously obtuse to rounded;

petals long-lasting, erect to erect-spreading, ± connivent, ± concealing stamens and ovary, white, occasionally purple stained basally, sometimes weakly spirally twisted, linear to linear-lanceolate, 2.2–4.5 × 0.4–1 cm, thin-textured, base occasionally cuneate, margins entire, apex obtuse;

stamens erect, 10–15.5 mm;

filaments white, greenish white, or purple stained, 1–3 mm, much shorter than anthers, slender;

anthers erect, straight, greenish white, 9–11+ mm, ± slender, dehiscence latrorse;

connective greenish, straight, barely extended (to 0.4 mm) beyond anther sacs;

ovary green or green and purple basally, ovoid, obscurely 6-gonal, 4–8 mm;

stigmas erect, ± divergent, distinct, green, outer surface purple, subulate, 3–4.5 mm, ± fleshy, thickened.

Fruits

red-purple, fragrance not reported, ovoid, obscurely 6-angled, 2.5–3 cm, pulpy, juicy.

dark reddish purple or maroon, fragrance not reported, subglobose, ± 1 cm, ± juicy.

2n

= 10.

= 10.

Trillium chloropetalum

Trillium parviflorum

Phenology Flowering spring (late Mar–early May).
Habitat Mature fir (Abies), spruce (Picea), and hardwood forests in rich humus with mosses, open, somewhat grassy large groves of old oaks, with considerable underbrush and rather few herbaceous companions, in tangled, wet stream-bank alders (Alnus sp.), grasses, open clay hillside soils among shrubs
Elevation 20–60 m (100–200 ft)
Distribution
from FNA
CA
[WildflowerSearch map]
[BONAP county map]
from FNA
OR; WA
Discussion

Varieties 2 (2 in the flora).

J. D. Freeman (1975) considered that Trillium chloropetalum differs from T. albidum in having introrse (not latrorse) anther sacs, and that the purple pigments present on anther and ovary tissue here are absent in T. albidum. In some places, hybridization between the two certainly has occurred, and a complete range of intergrades exists.

This species merits further study. The following varieties are only weakly differentiated and perhaps ought to be dropped.

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

Trillium parviflorum varies from very short, slender, small-bracted plants to tall, broad, umbrella-bracted giants. Regardless of plant or bract sizes, flower and petal sizes are remarkably constant, all plants having small, linear-lanceolate petals. This is not usually the case with T. albidum, the species with which this plant is most likely to be confused. In T. albidum also the plants can be enormous, but when they are, the petals are very long, broad, and conspicuously obovate-diamond-shaped. In large clonal clumps of T. albidum, the larger and more mature offsets show the typical petal shape, while the smaller and presumably youngest offsets sometimes produce smaller, narrower petals, more like those of T. parviflorum.

Some western botanists, more experienced with local populations than I, do not consider Trillium parviflorum to be distinct from T. albidum. They point out that since there is an extensive region of apparent intergradation (as indeed there is, well supported by herbarium vouchers), there exists a morphological cline from the long- and wide-petaled T. albidum to the narrower- and generally shorter-petaled T. parviflorum, and that T. parviflorum, therefore, should not be considered a separate species but rather a subspecies or a variety. Since no one to date has treated T. parviflorum at the subspecific or varietal level, and since in my own limited experience it does appear as a distinct species in Washington north of the Columbia River, I include it here as treated by Soukup. I have seen populations of considerable variation north of Corvallis, Oregon, and agree that there is much overlap with T. albidum. Obviously there is need for a much more extensive study of this situation.

A factor that exacerbates this problem (and many others in Trillium), is that nutrition, age, and even favorable position in the habitat can greatly influence plant and floral organ sizes. In many species, including T. albidum, when a single vigorous clonal clump produces many offsets, the oldest offsets may have flowers with very large petals, sepals, ovary, etc., while the younger offsets may have organs only half the size. In most sessile trilliums particularly, population averages are often more useful than isolated individual measurements, a difficult situation, indeed.

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

Key
1. Petal tissue always with yellow pigments, often present with other pigments; petals yellow, greenish yellow, greenish purple, or bronze-green or brown.
var. chloropetalum
1. Petal tissue lacking yellow pigments; petals purple, reddish purple, garnet red, pink, or greenish white.
var. giganteum
Source FNA vol. 26. FNA vol. 26, p. 113.
Parent taxa Liliaceae > Trillium > subg. Phyllantherum Liliaceae > Trillium > subg. Phyllantherum
Sibling taxa
T. albidum, T. angustipetalum, T. catesbaei, T. cernuum, T. cuneatum, T. decipiens, T. decumbens, T. discolor, T. erectum, T. flexipes, T. foetidissimum, T. gracile, T. grandiflorum, T. kurabayashii, T. lancifolium, T. ludovicianum, T. luteum, T. maculatum, T. nivale, T. ovatum, T. parviflorum, T. persistens, T. petiolatum, T. pusillum, T. recurvatum, T. reliquum, T. rivale, T. rugelii, T. sessile, T. simile, T. stamineum, T. sulcatum, T. underwoodii, T. undulatum, T. vaseyi, T. viride, T. viridescens
T. albidum, T. angustipetalum, T. catesbaei, T. cernuum, T. chloropetalum, T. cuneatum, T. decipiens, T. decumbens, T. discolor, T. erectum, T. flexipes, T. foetidissimum, T. gracile, T. grandiflorum, T. kurabayashii, T. lancifolium, T. ludovicianum, T. luteum, T. maculatum, T. nivale, T. ovatum, T. persistens, T. petiolatum, T. pusillum, T. recurvatum, T. reliquum, T. rivale, T. rugelii, T. sessile, T. simile, T. stamineum, T. sulcatum, T. underwoodii, T. undulatum, T. vaseyi, T. viride, T. viridescens
Subordinate taxa
T. chloropetalum var. chloropetalum, T. chloropetalum var. giganteum
Synonyms T. sessile var. chloropetalum, T. giganteum var. chloropetalum
Name authority (Torrey) Howell: Fl. N.W. Amer., 661. (1902) V. G. Soukup: Brittonia 32: 330, fig. 1. (1980)
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