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codlins-and-cream, fiddle grass, fiddle grass willowherb, great or great hairy willowherb, great willowherb, hairy willlowherb, hairy willow-herb, épilobe hirsute

alpine willow-herb, pimpernel willow-herb, épilobe à feuilles de mouron

Habit Herbs usually robust and rank, sometimes woody near base, with thick, ropelike stolons to 1 m with scattered cataphylls and, often, terminal leafy rosette. Herbs with spreading thin, small-leafed epigeous soboles to 5 cm.
Stems

erect to ascending, often clumped, terete, 25–120(–250) cm, unusually thick, 3–9 mm diam., well branched mainly in distal 1/2, densely long-villous throughout, usually mixed glandular puberulent distally, rarely sparsely villous or densely white-tomentose.

many, ascending, often sigmoidally bent, nodding distally, later erect, clumped or mat-forming, terete, 3–20(–25) cm, simple, subglabrous, sometimes with faint raised strigillose lines decurrent from margins of petioles, rarely mixed strigillose and sparsely glandular puberulent distally.

Leaves

opposite proximal to inflorescence, alternate distally, sessile and ± clasping stem;

blade elliptic-lanceolate to narrowly obovate or elliptic, 4–12(–23) × 0.3–4(–5) cm, base cuneate to attenuate, margins serrulate, 15–50 teeth per side, veins 6–9 per side, apex acute to acuminate or obtuse proximally, surfaces ± densely villous;

bracts moderately reduced.

opposite and crowded proximal to inflorescence, alternate distally, petioles 1–6 mm, rarely subsessile distally;

blade spatulate to oblong proximally, elliptic to narrowly lanceolate or sublinear distally, (0.5–)0.8–2.5 × 0.3–1 cm, base attenuate to cuneate, margins subentire proximally, sparsely denticulate distally with 2–5 low teeth per side, veins obscure, 2–4 per side, apex obtuse or rounded proximally to subacute distally, surfaces subglabrous;

bracts reduced, usually much narrower.

Inflorescences

erect racemes or panicles, usually densely villous and glandular puberulent, rarely tomentose.

nodding in bud, later suberect, few-flowered racemes, subglabrous to sparsely strigillose and/or glandular puberulent.

Flowers

erect;

buds 5–9 × 1.8–4.5 mm, sometimes beaked;

pedicel 3–11 mm;

floral tube 1.3–2.9 × 2.2–4 mm, conspicuous ring of spreading hairs near mouth inside;

sepals oblong-linear, often keeled, 6–12 × 1–3 mm, abaxial surface densely pubescent;

petals bright pink to rose-purple, rarely white, broadly obcordate, 9–20 × 7–15 mm, apical notch 1–3 mm;

filaments white or pink, those of longer stamens 5–10 mm, those of shorter ones 2.5–6 mm;

anthers cream, 1.5–3 × 0.6–1.2 mm;

ovary 15–34 mm, densely villous and glandular puberulent;

style white or pink, 5–12 mm, usually glabrous, stigma deeply 4-lobed, 1.8–2.2 × 3–5.5 mm, lobes recurved or spreading, exserted beyond anthers.

suberect;

buds 2–5 × 1–2 mm;

pedicel 1–6(–15) mm;

floral tube 0.6–1.2 × 0.8–1.8 mm, slightly raised subglabrous ring at mouth inside;

sepals green to reddish purple, 1.5–5 × 0.6–1.5 mm, abaxial surface subglabrous to sparsely glandular;

petals usually pink to rose-purple, rarely white, narrowly obcordate, (1.7–)2.5–6.5(–8) × 1.6–3.5 mm, apical notch 0.5–1.2 mm;

filaments cream to light pink, those of longer stamens 1.4–3.2 mm, those of shorter ones 0.7–2 mm;

anthers 0.3–0.6 × 0.2–0.4 mm;

ovary often reddish purple, 6–20 mm, subglabrous or sparsely strigillose and glandular puberulent;

style white, 1.2–2.5 mm, glabrous, stigma broadly clavate to subcapitate, entire, 0.9–1.5 × 0.4–0.7 mm, surrounded by longer anthers.

Capsules

often flushed purple, 25–90 mm, surfaces usually densely villous and glandular puberulent, rarely glabrescent;

pedicel 5–20 mm.

slender, often reddish purple, 17–40(–55) mm, surfaces subglabrous or with scattered hairs;

pedicel 5–35(–68) mm.

Seeds

narrowly obovoid, 0.8–1.2 × 0.3–0.6 mm, chalazal collar inconspicuous, dark brown, surface coarsely papillose;

coma easily detached, tawny or dull white, 7–10 mm.

narrowly obovoid, 0.7–1.4 × 0.3–0.5 mm, inconspicuous chalazal collar 0.1–0.2 mm wide, light brown, surface reticulate (smooth);

coma persistent, dull white, 2–4 mm.

2n

= 36.

= 36.

Epilobium hirsutum

Epilobium anagallidifolium

Phenology Flowering Jun–Sep. Flowering Jun–Sep.
Habitat Low wet areas along streams, rivers, ponds, and lakes, roadside ditches, along railroad tracks, marshes and swampy areas. Moist flats, stream banks, subarctic coastal marsh edges, high montane and alpine meadows and seeps.
Elevation 0–150[–3000] m. (0–500[–9800] ft.) 0–4500 m. (0–14800 ft.)
Distribution
from FNA
CO; CT; IL; IN; KY; MA; MD; ME; MI; NH; NJ; NY; OH; OR; PA; RI; UT; VT; WA; WI; WV; BC; NB; NS; ON; PE; QC; Eurasia; Africa [Introduced in North America]
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; CA; CO; ID; ME; MT; NH; NV; OR; UT; WA; WY; AB; BC; NL; NT; NU; QC; YT; Greenland; Eurasia
[WildflowerSearch map]
[BONAP county map]
Discussion

Epilobium hirsutum is very widespread in cool temperate Eurasia and montane regions, occurring throughout Europe except in the far north (P. H. Raven 1968), through the Caucasus and central Asia (E. I. Steinberg 1949) to Nepal (Raven 1962), China (Chen C. J. et al. 1992), and Japan (A. W. Lievens and P. C. Hoch 1999). It occurs as well along the Mediterranean coast of Africa, through East Africa to southern Africa, and in the Canary and Cape Verde Islands (Raven 1967).

Epilobium hirsutum exceeds almost all other species of the genus in stature, so its size, very large flowers, and densely villous aspect make it easy to identify. R. L. Stuckey (1970) provided a detailed account of the introduction and spread of E. hirsutum in North America, noting the earliest known collection (July 1829) was from Newport, Rhode Island. Most early collections appeared in waste areas, particularly near harbor ballast piles, although some may have been grown in gardens. By the 1890s this species was well established along the Atlantic coastal region from New Jersey and Philadelphia through New England, and around Niagara Falls in the Great Lakes region. During the twentieth century, E. hirsutum spread extensively in southern Ontario and Quebec, south along the Atlantic coast to Maryland, and to all of the states along the southern shores of the Great Lakes, most recently including Wisconsin (1970), and Indiana (1972). It occurs in much the same habitat as that of another, more widely publicized invader, Lythrum salicaria, and sometimes is recorded as a companion species. The earliest known collection in western North America was made in 1933 in Bingen (Klickitat County), Washington. Whether from that introduction or others, E. hirsutum is now naturalized and widespread in the Pacific Northwest. It also was reported recently from the Denver region in Colorado and near Midway in Utah.

Epilobium grandiflorum F. H. Wiggers and E. grandiflorum Allioni are illegitimate names that pertain here.

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

Epilobium anagallidifolium is widely but sparsely distributed in high montane-alpine and subarctic Eurasia, including Europe, Russia, China, and Japan.

Epilobium anagallidifolium usually forms low clumps or mats, with stems nodding in bud and usually subglabrous below the inflorescence. Many collections of E. anagallidifolium from eastern Canada and Greenland tend to be unusually tall (to 25 cm) and robust for the species, with somewhat larger, thicker leaves, and longer pedicels (to 60 mm). Similarly large and robust specimens occur scattered in Yukon and Washington, and may result from occasional hybridization and introgression with sympatric species such as E. hornemannii or E. lactiflorum, which also have the CC chromosomal arrangement. In an analysis of Fennoscandian populations of the Alpinae group, I. Kytövuori (1972) found a similar pattern of mostly smaller, sigmoidal plants of E. anagallidifolium with a small proportion of larger ones, and he also suggested the possibility of hybridization and/or introgression.

Plants of Epilobium anagallidifolium, and indeed of the whole Alpinae group, from Haida Gwaii (the Queen Charlotte Islands) of British Columbia (J. A. Calder and R. L. Taylor 1968), are particularly distinctive compared to those on the mainland, and difficult to interpret. The observed differences may be the result of hybridization with other sympatric species or a response to unique ecological conditions on the islands, reinforced by relative isolation from mainland British Columbia.

The Linnaean name Epilobium alpinum has long been a source of nomenclatural confusion and instability, since it circumscribed at least four distinct species, especially E. anagallidifolium. A proposal by P. C. Hoch et al. (1995) to permanently reject the name E. alpinum Linnaeus was approved.

(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. Epilobium Onagraceae > subfam. Onagroideae > tribe Epilobieae > Epilobium > sect. Epilobium
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. hornemannii, E. howellii, E. lactiflorum, E. leptocarpum, E. leptophyllum, E. luteum, E. minutum, 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
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. minutum, 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
Synonyms Chamaenerion hirsutum, E. amplexicaule, E. aquaticum, E. hirsutum var. villosum, E. villosum E. alpinum, E. pseudoscaposum
Name authority Linnaeus: Sp. Pl. 1: 347. (1753) Lamarck in J. Lamarck et al.: Encycl. 2: 376. (1786)
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