Flora of North America species comparison

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Epilobium minutum

Onagraceae tribe Epilobieae

California willowherb, chaparral willowherb, desert willowherb, little willowherb, minute willowherb, small-flower willowherb
Habit Herbs slender. Herbs, annual or perennial, sometimes suffrutescent.
Stems

strict, erect, sometimes reddish green, terete, 3.5–40 cm, simple or freely branched, subglabrous proximally to strigillose and glandular puberulent distally.

Leaves

alternate distally, not fasciculate, petiole 0–2 mm, blade subspatulate proximally to lanceolate, oblanceolate, or narrowly elliptical distally, not folded along midrib, 0.9–2.5 × 0.2–0.6 cm, shorter than internodes, base tapered, margins entire or scarcely denticulate, 1–4 teeth per side, lateral veins obscure, apex subacute or often blunt proximally, surfaces subglabrous or with scattered hairs along margins;

bracts much reduced, sometimes attached to pedicel.

opposite at least near base or throughout, alternate distally, or sometimes alternate throughout;

stipules absent.
Inflorescences

erect racemes or open panicles, relatively loose and uncrowded, branches thin, mixed strigillose and glandular puberulent.

Flowers

erect or, sometimes, nodding in bud;

buds broadly ovoid, 1.2–2.5 × 1–1.5 mm;

floral tube 1.1–1.5 × 1–1.4 mm, usually with ring of spreading hairs at mouth inside;

sepals 0.5–2.5 × 0.4–1.3 mm, apex acute, abaxial surface strigillose, sometimes mixed glandular puberulent;

petals white to pink, 2–5 × 1.5–3 mm, apical notch 0.2–1.9 mm;

filaments white, those of longer stamens 0.5–3 mm, those of shorter ones 0.3–2 mm;

anthers 0.6–1 × 0.5–0.8 mm;

ovary 4–9 mm, mixed strigillose and glandular puberulent;

style light pink, 1–3.5 mm, stigma subclavate to obscurely 4-lobed, 0.4–0.6 × 0.4–0.5 mm, surrounded by longer anthers.

actinomorphic or slightly zygomorphic, 4-merous;

sepals erect or spreading;

stamens 2 times as many as sepals;

pollen shed in tetrads or monads.
Fruit

a slender, cylindrical, loculicidal capsule.
Capsules

9–28 mm, surfaces strigillose and glandular puberulent;

pedicel 3–10 mm.

Seeds

obovoid, without constriction, 0.9–1.2 × 0.4–0.6 mm, low chalazal collar 0.1–0.2 mm wide, brown, surface reticulate;

coma easily detached, white, 2.5–3 mm.

(1 or) many per locule, with tuft of hairs (coma) at chalazal end, sometimes without coma.
2n

= 26.

Epilobium minutum

Onagraceae tribe Epilobieae
Phenology Flowering Apr–Sep.
Habitat Open, dry places, along roads, disturbed areas.
Elevation 90–1900 m. (300–6200 ft.)
Distribution
from FNA
CA; ID; MT; NV; OR; WA; BC
[WildflowerSearch map]
[BONAP county map]
North America; Mexico; Central America; South America; West Indies; Eurasia; Africa; Atlantic Islands; Australasia [Introduced in Pacific Islands]
Discussion

Epilobium minutum, like the similar E. foliosum, also occasionally produces cleistogamous flowers, and is modally autogamous in any event. S. R. Seavey et al. (1977b) observed that E. minutum is less common than E. foliosum in the southern part of their overlapping ranges and more common in the north. Several sheets (for example, Lawler 3276, California, Butte Co. [MO]; Nelson & Gordon 5573, California, Trinity Co. [MO]) mention that the plants were growing on serpentine soil. The earliest collection of this species appears to be one made by Archibald Menzies in 1792–1794 under the name E. palustre (BM).

Crossostigma lindleyi Spach (a substitute name for Epilobium minutum) and E. lindleyi (Spach) Rydberg are illegitimate names that pertain here.

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

Genera 2, species 173 (2 genera, 43 species in the flora).

Epilobium and its close relatives have been recognized historically either as part of Onagreae (A. P. de Candolle 1828b), sometimes as a subtribe (É. Spach 1834–1848, vol. 4; J. Torrey and A. Gray 1838–1843, vol. 1), or as the distinct Epilobieae (R. Raimann 1893; P. A. Munz 1965; P. H. Raven 1976). The synapomorphies for Epilobieae as currently delimited include its highly condensed, heteropycnotic chromosomes with a base chromosome number of x = 18, sepals held erect or spreading (not reflexed) throughout anthesis, and the presence of a coma of hairs on the seeds (secondarily lost in some species). Molecular support for the tribe is strong (97–100% BOOTSTRAP support; D. A. Baum et al. 1994; R. A. Levin et al. 2004).

Endlicher established Epilobieae and included Oenothera within it; it is unclear how or whether his concept differed from Onagreae of A. P. de Candolle (1828b). É. Spach (1834–1848, vol. 4) recognized these genera as Onagreae and differentiated so-called sect. Oenotherinae from sect. Epilobieae, placing in the latter not only Epilobium and related groups, but also Clarkia and its segregates. J. Torrey and A. Gray (1840) excluded Clarkia from their Epilobiinae and also excluded Boisduvalia, a delimitation also followed by R. Raimann (1893) for his Epilobieae. Epilobieae did not assume its current delimitation, including only Epilobium and its close relatives, until the works of P. A. Munz (1941) and P. H. Raven (1964).

G. L. Stebbins (1971) and P. H. Raven (1976) considered the diverse chromosome numbers in Epilobieae and proposed that the species of Boisduvalia (now a section of Epilobium) with n = 9 or 10 represented the original base chromosome number for the tribe, and that these numbers were derived from x = 11 which is found in Circaeeae, Gongylocarpeae, and Lopezieae (W. L. Wagner et al. 2007). They proposed a series of aneuploid reductions from n = 9 or 10 to n = 6, followed by polyploidy to produce the array of numbers in Epilobium (n = 12, 13, 15, 16, 18, 30) and Boisduvalia (n = 9, 10, 15, 19). D. A. Baum et al. (1994) demonstrated that molecular data did not support that hypothesis and found that a monophyletic Chamaenerion (n = 18, 36, 54) forms a strongly distinct sister branch to Epilobium, within which sect. Epilobium (n = 18) is monophyletic and sister to the rest of Epilobium, including the former segregates Boisduvalia and Zauschneria. The data from Baum et al. suggested that Epilobieae are primitively polyploid, with numbers based on x = 18, which is unique in the family. Using comparable sampling and some additional genes, R. A. Levin et al. (2004) found strong support for the phylogeny proposed by Baum et al.

(Discussion copyrighted by Flora of North America; reprinted with permission.)
Source FNA vol. 10. FNA vol. 10.
Parent taxa Onagraceae > subfam. Onagroideae > tribe Epilobieae > Epilobium > sect. Crossostigma Onagraceae > subfam. Onagroideae
Sibling taxa
E. anagallidifolium, E. arcticum, E. brachycarpum, E. campestre, E. canum, E. ciliatum, E. clavatum, E. cleistogamum, E. coloratum, E. davuricum, E. densiflorum, E. densum, E. foliosum, E. glaberrimum, E. hallianum, E. hirsutum, E. hornemannii, E. howellii, E. lactiflorum, E. leptocarpum, E. leptophyllum, E. luteum, E. mirabile, E. montanum, E. nevadense, E. nivium, E. obcordatum, E. obscurum, E. oreganum, E. oregonense, E. pallidum, E. palustre, E. parviflorum, E. rigidum, E. saximontanum, E. septentrionale, E. siskiyouense, E. smithii, E. suffruticosum, E. torreyi
Subordinate taxa
Synonyms E. minutum var. canescens Epilobioideae alph., Boisduvaliinae raimann, Epilobiinae torrey
Name authority Lindley in W. J. Hooker: Fl. Bor.-Amer. 1: 207. (1832) Endlicher: Fl. Poson., 366. (1830)
Web links 
Unless otherwise noted, all data comes from the online version of the Flora of North America, who have made most of their content available via a Creative Commons license (CC BY 4.0).



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