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glandular willowherb, Rocky Mountain willowherb, Rocky Mountain willowweed, épilobe des rocheuses

Nevada willowherb

Habit Herbs usually with sessile, fleshy, underground turions, or sometimes thick, elongated shoots with dark, decussate scales. Herbs with many shoots from thick, woody caudex.
Stems

erect, strict, terete, 4–55 cm, simple or well branched in age, subglabrous proximally to mixed strigillose and glandular puberulent distally, with raised strigillose lines decurrent from margins of petioles.

erect or ascending, terete, 10–50 cm, branched at base and apically, densely strigillose throughout, sometimes mixed villous distally.

Leaves

opposite proximal to inflorescence, alternate and reduced distally, often ± appressed, usually subsessile, rarely petiole 1–3 mm, often clasping;

blade obovate proximally to ovate, lanceolate, or narrowly elliptic distally, 1–5.5(–6.5) × 0.4–2(–2.4) cm, base rounded or obtuse, margins low denticulate, 9–30 teeth per side, veins ± conspicuous, 3–6 per side, apex subacute, surfaces subglabrous with strigillose margins;

bracts much reduced.

proximal pairs often early-deciduous, petiole 1–4 mm, blade lanceolate-elliptic to narrowly so, ± folded along midrib, 0.9–1.7 × 0.2–0.6 cm, shorter than internodes, base attenuate or narrowly cuneate, margins denticulate, 6–10 low teeth per side, lateral veins inconspicuous or absent, apex acute with deciduous, rigid mucronate gland, surfaces usually glabrescent with scattered hairs on abaxial midrib, rarely strigillose-villous throughout;

bracts much reduced, sublinear, often attached to pedicel.

Inflorescences

erect, sometimes nodding in bud, racemes, sometimes sparsely branched.

erect, open racemes or panicles, strigillose, often mixed glandular puberulent.

Flowers

erect;

buds 2–3.5 × 1.8–2.5 mm;

pedicel 0–1 mm;

floral tube 0.8–1.4 × 0.8–1.9 mm, ring of sparse spreading hairs at mouth inside;

sepals sometimes flushed red, 1.2–3.5 × 0.6–1.4 mm, abaxial surface strigillose and sometimes mixed glandular puberulent;

petals usually white, infrequently pink, 2.2–5(–7) × 1.7–3.2 mm, apical notch 0.4–1.5 mm;

filaments usually cream, rarely light pink, those of longer stamens 2–3.5 mm, those of shorter ones 1–2 mm;

anthers cream to light yellow, 0.3–0.8 × 0.3–0.5 mm;

ovary 9–30 mm, densely strigillose and glandular puberulent;

style cream or yellow, 1.6–2.8 mm, stigma usually narrowly to broadly clavate, rarely subcapitate, 1–3 × 0.8–2 mm, surrounded by at least longer anthers.

erect to ± nodding;

buds rounded-obovoid, 5–6 × 3–4 mm;

floral tube with slight constriction 2–3 mm distal to base, 2.7–3.2(–5) × 1.8–2.5(–3.1) mm, without ring or scales inside, glabrous;

sepals erect or sometimes deflexed in late anthesis, green or reddish green, lanceolate, 2.6–4.2 × 0.9–1.3 mm, apex acute;

petals deep rose-purple, obcordate, 5–7.2 × 3.2–4.1 mm, apical notch 2–3 mm;

filaments cream or white, those of longer stamens 5–7.5 mm, those of shorter ones 3.5–5.5 mm;

anthers cream, 1–1.8 × 0.5–0.8 mm, scarcely apiculate;

ovary 2.5–3.8 mm, densely strigillose and/or glandular puberulent;

style cream, 6–9.5 mm, glabrous, stigma 4-lobed, 0.8–1.2 × 1–1.5 mm, lobes reflexed or sometimes incompletely spread, then forming cup-like structure, exserted beyond longer anthers.

Capsules

30–55(–70) mm, surfaces mixed strigillose and glandular puberulent; usually subsessile, rarely pedicel 1–5 mm, often appressed to stem.

erect, subfusiform, 8–12 mm, surfaces strigillose and/or glandular puberulent;

pedicel 1–1.8 mm.

Seeds

very narrowly obovoid, 1–1.6(–1.8) × 0.4–0.6 mm, chalazal collar 0.1–0.2 mm, light brown or gray, surface rugose to papillose;

coma usually readily detached, white, 3–9 mm.

obovoid, with constriction 0.6–1 mm from micropylar end, 2.1–2.9 × 1.2–1.5 mm, very inconspicuous chalazal collar 0.05–0.06 mm wide, dark brown, surface low papillose, papillae often with central pit;

coma easily detached, white, 6–7.5 mm.

2n

= 36.

= 30.

Epilobium saximontanum

Epilobium nevadense

Phenology Flowering Jul–Sep. Flowering Jul–Sep.
Habitat Montane semi-shaded stream banks, damp meadows, mossy seeps, wet slatey cliffs, disturbed or seasonally damp areas. Loose scree slopes, limestone talus, sandy soils at base of steep rock faces in pinyon pine-juniper-mountain brush communities.
Elevation 0–3700 m. (0–12100 ft.) 1800–2800 m. (5900–9200 ft.)
Distribution
from FNA
AZ; CA; CO; ID; MT; NM; NV; OR; SD; UT; WY; AB; BC; MB; NF; ON; QC
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; NV; UT
[BONAP county map]
Discussion

Epilobium saximontanum is morphologically similar to E. ciliatum (especially subsp. glandulosum) with which it also shares the AA chromosome arrangement. However, in addition to its fleshy compact turions, it very characteristically has notably appressed capsules, unlike most other species in the genus, and a notably strict habit.

The distribution of Epilobium saximontanum is unusual; it includes the Rocky Mountain region, only barely reaching the high southern Sierra Nevada, disjunct to the Black Hills of South Dakota, and more widely in eastern Canada, from the shores of Hudson Bay to Newfoundland. Specimens are fairly uniform across this wide and rather discontinuous range, although locally they show some variability, possibly due to hybridization with any of several species that may be sympatric with it. H. Lewis and D. M. Moore (1962) reported hybrids between E. saximontanum (cited as E. brevistylum) and E. ciliatum subsp. ciliatum (cited as E. adenocaulon) from Colorado, and herbarium specimens with E. saximontanum and apparent hybrids are not uncommon.

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

In his description of Epilobium nevadense, Munz clearly recognized its affinity to E. nivium and suggested a close relationship between these two species and E. brachycarpum, based on similarities in seed and floral morphology. S. R. Seavey and P. H. Raven (1977c) demonstrated the close affinity between E. nivium and E. nevadense by forming fully fertile (99%) hybrids. However, compared to E. nivium, E. nevadense has denticulate, subglabrous leaves (versus subentire, densely pubescent leaves) and shorter floral tube [2.7–3.2(–5) mm] versus longer (5.2–9.5 mm) in E. nivium; furthermore, the two have completely non-overlapping geographical ranges. In overall morphology and cytology, these two species (and the somewhat more distantly related E. suffruticosum) are quite distinct from the rest of the genus.

Originally known only from the Charleston Mountains in southern Nevada, Epilobium nevadense has since been collected in northern Arizona, Eureka and Lincoln counties in Nevada, and in three counties of southwestern Utah. It may be more widespread in this region, much of which (especially in southern Nevada) consists of military reserves that are inaccessible to collectors. Although it was at one time considered endangered (S. D. Ripley 1975) due to the relatively low number of collections and threats from increased recreational use in its area of occurrence, it is no longer considered a candidate for listing (http://endangered.fws.gov). Several collections of this species show evidence of seed predation, apparently by moth larvae (H. N. Mozingo and Margaret Williams 1980), and S. R. Seavey and P. H. Raven (1977c) reported that larvae found in capsules from the locality in the Charleston Mountains were identified as Mompha (Momphidae, Gelechioidea).

(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. Cordylophorum > subsect. Petrolobium
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. 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. septentrionale, E. siskiyouense, E. smithii, E. suffruticosum, E. torreyi
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. minutum, E. mirabile, E. montanum, 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 E. adenocaulon subsp. rubescens, E. drummondii, E. drummondii var. latiusculum, E. latiusculum, E. ovatifolium, E. rubescens, E. scalare, E. stramineum
Name authority Haussknecht: Oesterr. Bot. Z. 29: 119. (1879) Munz: Bull. Torrey Bot. Club 56: 166. (1929)
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