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diamond-leaf willow, plane-leaf willow, tea-leaf willow, tea-leafed willow

Alaska bog willow

Habit Shrubs or trees, 0.1–9 m, (sometimes forming clones by layering). Plants 0.15–0.55 m, forming clones by layering.
Stems

(sometimes decumbent);

branches yellow-brown, red-brown, or violet, not to strongly glaucous, glabrous or pubescent;

branchlets yellow-brown, red-brown, or violet, glabrous, pilose, pubescent, moderately densely villous, or short-silky, (buds caprea-type).

decumbent or trailing;

branches yellow-brown, glabrous;

branchlets red-brown, gray-brown, or yellow-brown, glabrous.

Leaves

stipules (sometimes marcescent), rudimentary or foliaceous (small and usually brownish) on early ones, rudimentary or foliaceous on late ones, (narrowly ovate to oblong, 1–2.5(–4.5) mm), apex acute;

petiole shallowly grooved adaxially, 2–9(–13) mm, glabrous, pilose, or short-silky adaxially;

largest medial blade (sometimes hemiamphistomatous), narrowly oblong, narrowly elliptic, elliptic, or oblanceolate, 20–36–65 × 5–13–23 mm, 1.7–2.8–4.7 times as long as wide, base cuneate or convex, margins sometimes slightly revolute basally, entire, or, sometimes, crenulate or serrulate, apex acute, acuminate, or convex, abaxial surface glaucous, glabrous or sparsely silky, hairs (white, sometimes also ferruginous) straight or wavy, adaxial highly glossy, glabrous or sparsely short-silky;

proximal blade margins entire;

juvenile blade reddish or yellowish green, glabrous, puberulent, pubescent, or densely long-silky abaxially, hairs white, sometimes also ferruginous.

stipules absent or rudimentary;

petiole 2–5.6(–6.4) mm;

largest medial blade hypostomatous, narrowly oblong, oblong, obovate, or broadly obovate, (14–)17–27(–45) × 7–21 mm, 1.4–2.5 times as long as wide, base cuneate or convex, margins slightly revolute or flat, entire, or serrulate to crenate proximally, (glands marginal), apex convex, acuminate, or rounded, abaxial surface glaucous, glabrous, adaxial slightly or highly glossy, glabrous;

proximal blade margins entire, (sometimes hairs ferruginous abaxially);

juvenile blade glabrous.

Staminate flowers

adaxial nectary narrowly oblong or oblong, 0.4–1.1 mm;

filaments distinct, glabrous or sparsely hairy basally;

anthers purple turning yellow, shortly cylindrical, 0.5–0.7 mm.

abaxial nectary absent, adaxial nectary oblong, 0.5–0.8 mm;

filaments distinct or connate less than 1/2 their lengths, glabrous;

anthers ellipsoid or shortly cylindrical, 0.3–0.4 mm.

Pistillate flowers

adaxial nectary oblong, square, or ovate, 0.4–1.3 mm, shorter to longer than stipe;

stipe 0.3–0.8 mm;

ovary pyriform, short- to long-silky, sometimes slightly bulged below styles;

ovules 11–16 per ovary;

styles 0.5–2 mm;

stigmas slenderly to broadly cylindrical, 0.36–0.52–1.1 mm.

abaxial nectary absent, adaxial nectary oblong, 0.4–0.9 mm, shorter than stipe;

stipe 0.8–2.5 mm;

ovary obclavate, pubescent or short-silky to glabrescent, hairs (often ferruginous), flattened or ribbonlike, beak abruptly tapering to styles;

ovules 8–12 per ovary;

styles connate or distinct distally, 0.1–0.4(–0.65) mm;

stigmas slenderly or broadly cylindrical, 0.24–0.3–0.68 mm.

Capsules

(2.5–)5.5–6 mm.

5.5–8 mm.

Catkins

flowering before leaves emerge; staminate stout, subglobose, or globose, 12–41 × 10–20 mm, flowering branchlet 0–4 mm; pistillate densely flowered, slender, or stout to globose, 15–67(–70 in fruit) × 8–18 mm, flowering branchlet 0–6 mm;

floral bract dark brown or black, 1–3.2 mm, apex acute, convex, or rounded, sometimes 2-fid, abaxially hairy, hairs straight.

staminate 8–58 × 5–19 mm, flowering branchlet 0.5–15 mm; pistillate moderately densely to loosely flowered, slender, stout, or subglobose, 13.5–64(–70 in fruit) × 6.5–15 mm, flowering branchlet 4–18 mm;

floral bract brown or bicolor, 0.8–1.6 mm, apex rounded, entire, abaxially sparsely hairy, hairs (usually white, sometimes also ferruginous), wavy or straight.

2n

= 76, 57.

= 38.

Salix planifolia

Salix fuscescens

Phenology Flowering early May-late Jun. Flowering Jun-late Jul.
Habitat Arctic, alpine, subalpine, and boreal meadows and riverbanks, streams, seeps, snowflush areas, treed bogs, fens, sandy-loam, rocky igneous and limestone substrates Bogs, treed bogs, sedge fens, poorly drained lakeshores, wet tundra, silt or fine sandy-gravel substrates
Elevation 100-4000 m (300-13100 ft) 50-1000 m (200-3300 ft)
Distribution
from FNA
AK; AZ; CA; CO; ID; ME; MI; MN; MT; NH; NM; NV; OR; SD; UT; VT; WA; WI; WY; AB; BC; MB; NL; NT; NU; ON; QC; SK; YT; SPM
[WildflowerSearch map]
[BONAP county map]
from FNA
AK; MB; NT; NU; YT; e Asia (Chukotka, Japan [Hokkaido], North Korea, Russian Far East, arctic, e Siberia)
[BONAP county map]
Discussion

Variety monica applies to the diminutive alpine form that sometimes is recognized in the southern Rocky Mountains (S. J. Brunsfeld and F. D. Johnson 1985); it occurs at higher elevations (2200–4000 m) and is characterized by low growth form (0.14–1 m) and smaller, slightly broader leaves. Although it can be distinctive, it is morphologically confluent with the typical species. B. G. O. Floderus (1939) may be correct in characterizing it as an alpine ecotype.

Salix planifolia and S. pulchra are closely related. Their ranges overlap in northwestern Canada, from northern British Columbia across the southern quarter of the Yukon and northeastward into the Great Bear Lake area. Specimens identified as S. pulchra occur as far northeastward as Coppermine and northeast of Bathurst Inlet; S. planifolia has been recognized in the Mackenzie Delta and Eskimo Lake regions, Northwest Territories. Outlying records should be treated with caution because identification of individual specimens out of context may not be definitive. G. W. Argus (1969, 1973) treated these taxa as subspecies based on their intergradation in northwestern British Columbia, their tetraploid chromosome number, and their similar leaf flavonoid chromatographic patterns, but this taxonomy needs reconsideration.

The primary differences between the two species are stipule size, shape, and persistence and the pubescence on juvenile leaves. Stipules of Salix planifolia are oblong to narrowly elliptic or obovate, 0.8–3 mm (or –4.5 mm at Back River, Northwest Territories), distinctly shorter than petioles, and rarely marcescent for more than one year; stipules of S. pulchra are linear to narrowly oblong, 3–32 mm, usually longer than petioles, and usually marcescent for two or more years. Juvenile leaves of S. planifolia are usually more densely hairy, but vary from glabrescent to sparsely or very densely pubescent or long-silky, whereas juvenile leaves of S. pulchra are usually glabrous or, sometimes, sparsely hairy. The occurrence of rhombic mature leaf blades in S. pulchra sometimes is distinctive, but overlap in leaf shape between the two taxa is very great.

The area of geographic overlap in Yukon and western Northwest Territories is large, but evidence suggests that there the two species may be separated by elevation. In the vicinity of Whitehorse, Yukon, Salix pulchra occurs at higher elevations (1400–1900 m) than S. planifolia (ca. 1000 m); no mixed populations were seen. In Nahanni National Park, Northwest Territories, where S. planifolia is more common than S. pulchra, the latter occurs only in alpine and subalpine habitats (1200–1400 m). Evidence from both localities indicates an elevational separation of the two taxa. Within the area of overlap there is little evidence of intergradation except that S. planifolia has stipules that tend to be more marcescent (40% are marcescent) and sometimes longer (2–3.5 mm) than is usual outside the area of overlap. Nevertheless, specimens from the area of overlap can be easily assigned to one taxon or the other with only a few apparent intermediates. The problem in recognizing intermediacy is that there are only a few, variable characters that separate the two. In contrast, in 1973, G. W. Argus described evidence of hybridization and introgression along the Haines Road in northwestern British Columbia. This was based on variation in stipule size, presence, and persistence in what appeared to be a hybrid swarm. Further data are needed to answer questions about actual hybridization. Are the species separated by habitat or elevation, and are there reproductive barriers? Answers could be gained by population studies and controlled hybridization. Until that is done it is best to treat these taxa as species.

See 76. Salix discolor and 95a. S. alaxensis var. alaxensis for comparative descriptions.

Hybrids:

Salix planifolia forms natural hybrids with S. alaxensis var. alaxensis, S. argyrocarpa, S. brachycarpa var. brachycarpa, S. candida, S. drummondiana, S. humilis, S. pellita, S. pulchra, and S. scouleriana. Hybrids with S. glauca var. cordifolia have been reported (C. K. Schneider 1921) but no convincing specimens have been seen.

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

Hybrids:

Salix fuscescens forms natural hybrids on the arctic coast of Alaska with S. arctica, S. ovalifolia, and S. phlebophylla, and in continental Nunavut with S. herbacea. These hybrids are not usually recognized but they appear sporadically.

Salix fuscescens × S. herbacea has crenate margins and is often confused with the latter species.

Some specimens identified as Salix fuscescens × S. ovalifolia are similar to hybrids with S. phlebophylla, but they lack marcescent leaves.

Salix fuscescens × S. phlebophylla has obovate leaves with one or two pairs of serrulations proximally, and glaucous abaxially as in S. fuscescens, but it grows in relatively dry tundra and has the marcescent, sometimes skeletonized, leaves of S. phlebophylla.

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

Source FNA vol. 7, p. 138. FNA vol. 7, p. 72.
Parent taxa Salicaceae > Salix > subg. Vetrix > sect. Phylicifoliae Salicaceae > Salix > subg. Chamaetia > sect. Myrtosalix
Sibling taxa
S. alaxensis, S. alba, S. amygdaloides, S. arbusculoides, S. arctica, S. arctophila, S. argyrocarpa, S. arizonica, S. athabascensis, S. atrocinerea, S. aurita, S. babylonica, S. ballii, S. barclayi, S. barrattiana, S. bebbiana, S. bonplandiana, S. boothii, S. brachycarpa, S. breweri, S. calcicola, S. candida, S. caprea, S. caroliniana, S. cascadensis, S. chamissonis, S. chlorolepis, S. cinerea, S. columbiana, S. commutata, S. cordata, S. daphnoides, S. delnortensis, S. discolor, S. drummondiana, S. eastwoodiae, S. elaeagnos, S. eriocephala, S. euxina, S. exigua, S. famelica, S. farriae, S. floridana, S. fuscescens, S. geyeriana, S. glauca, S. gooddingii, S. hastata, S. herbacea, S. hookeriana, S. humboldtiana, S. humilis, S. interior, S. irrorata, S. jejuna, S. jepsonii, S. laevigata, S. lasiandra, S. lasiolepis, S. lemmonii, S. ligulifolia, S. lucida, S. lutea, S. maccalliana, S. melanopsis, S. monochroma, S. monticola, S. myricoides, S. myrsinifolia, S. myrtillifolia, S. nigra, S. niphoclada, S. nivalis, S. nummularia, S. orestera, S. ovalifolia, S. pedicellaris, S. pellita, S. pentandra, S. petiolaris, S. petrophila, S. phlebophylla, S. polaris, S. prolixa, S. pseudomonticola, S. pseudomyrsinites, S. pulchra, S. purpurea, S. pyrifolia, S. raupii, S. reticulata, S. richardsonii, S. rotundifolia, S. scouleriana, S. sericea, S. serissima, S. sessilifolia, S. setchelliana, S. silicicola, S. sitchensis, S. sphenophylla, S. stolonifera, S. taxifolia, S. thurberi, S. tracyi, S. triandra, S. turnorii, S. tweedyi, S. tyrrellii, S. uva-ursi, S. vestita, S. viminalis, S. wolfii, S. ×fragilis, S. ×jesupii, S. ×pendulina, S. ×sepulcralis, S. ×smithiana
S. alaxensis, S. alba, S. amygdaloides, S. arbusculoides, S. arctica, S. arctophila, S. argyrocarpa, S. arizonica, S. athabascensis, S. atrocinerea, S. aurita, S. babylonica, S. ballii, S. barclayi, S. barrattiana, S. bebbiana, S. bonplandiana, S. boothii, S. brachycarpa, S. breweri, S. calcicola, S. candida, S. caprea, S. caroliniana, S. cascadensis, S. chamissonis, S. chlorolepis, S. cinerea, S. columbiana, S. commutata, S. cordata, S. daphnoides, S. delnortensis, S. discolor, S. drummondiana, S. eastwoodiae, S. elaeagnos, S. eriocephala, S. euxina, S. exigua, S. famelica, S. farriae, S. floridana, S. geyeriana, S. glauca, S. gooddingii, S. hastata, S. herbacea, S. hookeriana, S. humboldtiana, S. humilis, S. interior, S. irrorata, S. jejuna, S. jepsonii, S. laevigata, S. lasiandra, S. lasiolepis, S. lemmonii, S. ligulifolia, S. lucida, S. lutea, S. maccalliana, S. melanopsis, S. monochroma, S. monticola, S. myricoides, S. myrsinifolia, S. myrtillifolia, S. nigra, S. niphoclada, S. nivalis, S. nummularia, S. orestera, S. ovalifolia, S. pedicellaris, S. pellita, S. pentandra, S. petiolaris, S. petrophila, S. phlebophylla, S. planifolia, S. polaris, S. prolixa, S. pseudomonticola, S. pseudomyrsinites, S. pulchra, S. purpurea, S. pyrifolia, S. raupii, S. reticulata, S. richardsonii, S. rotundifolia, S. scouleriana, S. sericea, S. serissima, S. sessilifolia, S. setchelliana, S. silicicola, S. sitchensis, S. sphenophylla, S. stolonifera, S. taxifolia, S. thurberi, S. tracyi, S. triandra, S. turnorii, S. tweedyi, S. tyrrellii, S. uva-ursi, S. vestita, S. viminalis, S. wolfii, S. ×fragilis, S. ×jesupii, S. ×pendulina, S. ×sepulcralis, S. ×smithiana
Synonyms S. monica, S. phylicifolia var. monica, S. phylicifolia subsp. planifolia, S. planifolia var. monica S. fuscescens var. reducta
Name authority Pursh: Fl. Amer. Sept. 2: 611. (1813) Andersson: Monogr. Salicum, 97. (1867)
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