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

Barclay's willow

Habit Shrubs or trees, 0.1–9 m, (sometimes forming clones by layering). Plants (0.3–)1–3(–5) m. Stems: branches usually red-brown, sometimes yellow-brown, not to strongly glaucous, glabrous or villous; branchlets yellow-green, yellow-brown, or red-brown, densely villous to pubescent, (buds caprea-type, inner membranaceous bud-scale layer free, separating from outer layer).
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).

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 foliaceous, (2–14 mm), apex rounded or acuminate;

petiole shallowly grooved, or convex to flat adaxially, 3–14(–20) mm, villous or pilose adaxially;

largest medial blade oblong, narrowly elliptic, elliptic, oblanceolate, or obovate, 33–70(–100) × 12–35(–48) mm, 1.6–2.8(–4) times as long as wide, base usually rounded or convex, sometimes subcordate, margins slightly revolute or flat, serrulate, apex acute, acuminate, or convex, abaxial surface glaucous, glabrous or glabrescent, hairs straight, adaxial slightly glossy or dull, glabrous or pilose, midrib pilose;

proximal blade margins serrulate or entire;

juvenile blade sometimes reddish, densely villous or glabrous abaxially, hairs white.

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.

adaxial nectary oblong, 0.5–1 mm;

filaments distinct, glabrous;

anthers yellow, 0.6–1 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.

adaxial nectary oblong or ovate, 0.4–0.8 mm, shorter than or equal to stipe;

stipe 0.4–1.5 mm;

ovary obclavate or pyriform, glabrous, beak gradually tapering to styles;

ovules 18–24 per ovary;

styles 0.6–2.5 mm;

stigmas slenderly cylindrical, 0.28–0.48–0.72 mm.

Capsules

(2.5–)5.5–6 mm.

3–8 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.

flowering as leaves emerge; staminate stout, 13–60 × 10–25 mm, flowering branchlet 0–17 mm; pistillate moderately densely flowered, stout, subglobose, or slender, 26–80 × 9–18 mm, flowering branchlet 4–24 mm;

floral bract brown or black, 1.6–2.8 mm, apex acute or rounded, abaxially hairy, hairs straight, wavy, or curly.

2n

= 76, 57.

= 76 (based on putative Salix barclayi × S. barrattiana, see below).

Salix planifolia

Salix barclayi

Phenology Flowering early May-late Jun. Flowering late May-early Aug.
Habitat Arctic, alpine, subalpine, and boreal meadows and riverbanks, streams, seeps, snowflush areas, treed bogs, fens, sandy-loam, rocky igneous and limestone substrates Lake and streamshores, fens, moist to mesic forest openings, subalpine and alpine slopes, glacial moraines
Elevation 100-4000 m (300-13100 ft) 0-2800 m (0-9200 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
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[BONAP county map]
from FNA
AK; ID; MT; OR; WA; WY; AB; BC; NT; YT
[WildflowerSearch map]
[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.)

Vegetative specimens of Salix hastata often are misidentified as S. barclayi. The characters that indicate S. hastata, or sometimes possible hybrids, are the presence of ferruginous hairs on juvenile leaves or adaxial midribs of mature leaves, leaf margins often entire or with teeth present only distally, and buds with inner membranaceous layer not separating from outer layer.

Salix barclayi is distinguished from S. farriae and S. hastata by having bud-scales with inner membranaceous layer separating from outer layer, juvenile blades glabrous, pilose, or moderately densely villous, largest medial blades oblong, narrowly elliptic, elliptic, oblanceolate, or obovate, margins always toothed, pistillate flowering branchlets 4–24 mm, staminate flowering branchlets 0–17 mm, floral bracts brown to black, moderately densely hairy, anthers 0.6–1 mm, styles 0.6–2.5 mm, and stipes 0.4–1.5 mm; S. farriae has bud-scales with inner membranaceous layer separating from outer layer, juvenile blades glabrous or sparsely villous, largest medial blades narrowly elliptic to elliptic, margins usually entire, pistillate flowering branchlets 1.5–14 mm, staminate flowering branchlets 1–5 mm, floral bracts bicolor, brown, or black, sparsely hairy, anthers 0.3–0.6 mm, styles 0.3–1.2 mm, and stipes 0.5–1.2 mm; and S. hastata has bud-scales with inner membranaceous layer not separating from outer layer, juvenile blades sparsely pubescent, largest medial blades narrowly to broadly elliptic, narrowly ovate, or ovate, margins usually entire, pistillate flowering branchlets 1.5–9 mm, staminate flowering branchlets 1–7 mm, floral bracts brown or bicolor, sparsely hairy, anthers 0.4–0.6 mm, styles 0.2–0.48 mm, and stipes 0.4–1.2 mm.

Hybrids:

Salix barclayi is morphologically highly variable. While it is possible that much of this variability is inherent, hybridization and introgression have played an important role.

Salix barclayi forms natural hybrids with S. arctica, S. barrattiana, S. brachycarpa, S. cascadensis, S. commutata, S. farriae, S. hastata, S. hookeriana, S. richardsonii, and S. stolonifera.

Salix barclayi × S. barrattiana is characterized by oily buds that stain the pressing paper yellow, and leaves often entire, or nearly so, and closely gland-dotted, and not glaucous abaxially. Some hybrids resemble S. barclayi in having ovaries glabrous and leaves serrulate and slightly glaucous abaxially, while others resemble S. barrattiana in having stipules marcescent and leaves short-hairy on both surfaces and not glaucous abaxially, but it is the presence of the oily buds characteristic of S. barrattiana that indicates their hybridity. The hybrids usually were from populations that included both parents. An important ramification of the discovery of this hybrid is that the specimen on which the chromosome number for S. barclayi (R. D. Dorn 1976) is based is a plant with oily buds, which has leaves with a mixture of weakly developed teeth and closely gland-dotted, entire margins, and is putatively identified as this hybrid. Further chromosome counts for S. barclayi are needed. Hybrids are known in British Columbia from the mountains in the Peace and Liard river basins, and in Mt. Robson National Park. The hybrid should be suspected wherever the parents occur together.

Salix barclayi × S. cascadensis, collected in Washington in alpine mats growing with both parents, has ovaries with hairy beaks indicating hybridization.

Salix barclayi × S. commutata resembles S. barclayi in having leaves glaucous abaxially, and S. commutata in having leaves hairy on both surfaces (northern British Columbia, Unalaska Island, and southeastern Alaska).

Salix barclayi × S. farriae is represented by a series of specimens resembling S. barclayi but with ferruginous hairs on juvenile leaves or on adaxial midribs of mature leaves, found from the Rocky Mountains of Alberta to southern Yukon and adjacent Northwest Territories. Similar specimens from Alaska may be the hybrid S. barclayi × S. hastata. Both of these hybrids require further study. See 63. S. hastata and 64. S. farriae.

Salix barclayi × S. hookeriana hybrids or introgressants at Tanis Lake, Alaska, have subentire leaves and stipes glabrous or hairy.

Salix barclayi × S. richardsonii hybrids and intergrades are relatively common in Alaska, British Columbia, and Yukon. They resemble S. barclayi in having catkins borne on distinct flowering branchlets, small stipules, anthers yellow and longer, and S. richardsonii in having marcescent stipules, branchlets and branches coarsely villous with spreading hairs, pistillate nectaries longer than stipes, and catkins sometimes on relatively short flowering branchlets.

Salix barclayi × S. scouleriana has the general appearance of S. barclayi but the densely hairy ovaries and the relatively long stigmas (0.9–0.92 mm) of S. scouleriana. It was growing with S. barclayi in openings created in white spruce by bark beetles.

Salix barclayi × S. stolonifera is characterized by relatively small leaves with irregularly serrulate margins, some young leaves reddish green, and a prostrate habit (G. W. Argus 1973).

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

Source FNA vol. 7, p. 138. FNA vol. 7, p. 113.
Parent taxa Salicaceae > Salix > subg. Vetrix > sect. Phylicifoliae Salicaceae > Salix > subg. Vetrix > sect. Hastatae
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. 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. 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
Name authority Pursh: Fl. Amer. Sept. 2: 611. (1813) Andersson: Öfvers. Kongl. Vetensk.-Akad. Förh. 15: 125. (1858)
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