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sandbar willow

Pacific willow (var. lasiandra), shining willow, whiplash willow (ssp. caudata)

Habit Shrubs or trees, 4–9 m. Stems: branches gray-brown to red-brown, glabrous or villous; branchlets yellow brown to red-brown, densely tomentose or villous to glabrescent. Shrubs or trees, 4–6 m. Stems: branches flexible to highly brittle at base, yellow-brown, gray-brown, or red-brown, slightly to highly glossy, glabrous or villous to glabrescent; branchlets yellow-brown, gray-brown, or red-brown, glabrous, pilose, densely villous, or velvety, hairs spreading, straight, wavy, or crinkled.
Leaves

stipules absent or rudimentary on early ones, rudimentary or foliaceous on late ones;

petiole 1–5(–9) mm, glabrous or sparsely villous adaxially;

largest medial blade linear to lorate, 60–160 × 4–11 mm, (6.5–)11–19(–31) times as long as wide, base cuneate, margins flat, remotely spinulose-serrulate (teeth 2–5 per cm), apex acute or subacuminate, abaxial surface thinly glaucous, densely villous or long-silky to glabrescent, adaxial slightly glossy, pilose or densely villous to glabrescent;

proximal blade margins entire;

juvenile blade reddish or yellowish green, moderately densely to sparsely long-silky abaxially.

stipules foliaceous, apex convex to rounded;

petiole shallowly to deeply grooved adaxially, 5–13 mm, with clusters of spherical or foliaceous glands distally, glabrous, pilose, or densely villous adaxially;

largest medial blade usually hypostomatous or hemiamphistomatous, rarely amphistomatous, lorate, very narrowly elliptic, narrowly elliptic, or lanceolate, (24–)55–133 × 11–43 mm, 2.5–6.2 times as long as wide, base convex or cuneate, margins flat, serrulate, apex acuminate to caudate, abaxial surface usually not glaucous (rarely so), glabrous, pilose, or moderately densely villous or long-silky, hairs appressed or spreading, white and/or ferruginous, straight or wavy, (coarse, caducous), adaxial (secondary veins flat or protruding), slightly or highly glossy, glabrous, pilose, or long-silky, hairs white and/or ferruginous;

proximal blade margins entire and glandular-dotted, or serrulate or crenulate;

juvenile blade reddish or yellowish green, glabrous or densely villous or long-silky abaxially, hairs white and ferruginous.

Staminate flowers

abaxial nectary 0.5–1.1 mm, adaxial nectary ovate, narrowly oblong, or flask-shaped, 0.6–1.4 mm, nectaries distinct;

filaments hairy;

anthers 0.4–0.9 mm.

abaxial nectary 0.5–1.1 mm, adaxial nectary square or ovate, 0.3–0.9 mm, nectaries connate and cup-shaped;

stamens 3–6;

filaments distinct, hairy on proximal 1/2 or basally;

anthers ellipsoid, shortly cylindrical, obovoid, or globose, 0.6–0.8 mm.

Pistillate flowers

adaxial nectary narrowly oblong, 0.4–1.1 mm, shorter to longer than stipe;

stipe 0.4–0.8 mm;

ovary obclavate to pyriform, glabrous, glabrescent, or long-silky, beak abruptly tapering to styles;

ovules 16–36 per ovary;

styles 0–0.2 mm;

stigmas flat, abaxially non-papillate with pointed tip, or broadly cylindrical, 0.3–0.7 mm.

adaxial nectary square or ovate, (swollen), 0.2–0.5 mm, shorter than stipe;

stipe 0.5–2 mm;

ovary pyriform, beak slightly bulged below or gradually tapering to styles;

ovules 18–24 per ovary;

styles connate or distinct 1/2 their lengths, 0.5–0.8 mm;

stigmas flat, abaxially non-papillate with rounded tip, broadly cylindrical, or 2 plump lobes, 0.24–0.31–0.42 mm.

Capsules

(4–)5–8(–10) mm.

5–7 mm.

Catkins

(flowering throughout season); staminate 20–61 × 4–10 mm, flowering branchlet 3–20 mm; pistillate loosely flowered, slender or stout, 20–67 × 5–9 mm, flowering branchlet 3–19 mm;

floral bract (sometimes greenish), 1.5–3.5 mm, apex acute, acuminate, or rounded, entire, erose, or toothed, abaxially hairy either proximally or distally, hairs wavy.

staminate 19–69 × 4–14 mm, flowering branchlet 5–23 mm; pistillate (fruiting in summer), moderately densely to loosely flowered, slender to stout, 23–56(–70 in fruit) × 8–12 mm, flowering branchlet 8–25 mm;

floral bract 1.5–3 mm, apex convex or rounded, entire or toothed, abaxially sparsely hairy throughout or proximally, hairs wavy.

2n

= 38.

= 76.

Salix interior

Salix lucida

Phenology Flowering early Apr-early Jul. Flowering early May-mid Jul.
Habitat Sandy to silty flood plains, margins of lakes, ponds, and prairie sloughs, dry prairie sand hills, marshes, disturbed areas Sandy or gravelly floodplains, lake margins, sedge meadows, vernal pools, alvars, open fens, marl bogs, treed bogs
Elevation 10-1800 m (0-5900 ft) 0-600 m (0-2000 ft)
Distribution
from FNA
AK; AR; CO; CT; DC; DE; IA; IL; IN; KS; KY; LA; MD; ME; MI; MN; MO; MS; MT; ND; NE; NJ; NY; OH; OK; PA; SD; TN; TX; VA; WI; WV; WY; AB; BC; MB; NB; NT; ON; QC; SK; YT; Mexico (Tamaulipas, Veracruz)
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from FNA
CT; DE; IA; IL; IN; MA; MD; ME; MI; MN; ND; NH; NJ; NY; OH; PA; RI; SD; VA; VT; WI; WV; MB; NB; NL; NS; ON; PE; QC; SK; SPM
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Discussion

Sometimes Salix interior is treated as a subspecies of S. exigua (R. D. Dorn 1998). Salix exigua and S. interior hybridize and apparently intergrade in the western Great Plains; because the area of overlap is relatively small and distinctiveness of the two taxa is not compromised by hybridization and introgression, it is best to treat them as separate species.

Leaves on sylleptic shoots are usually very densely silky. Salix interior sometimes has shoots that arise from buds on either side of the normal axillary bud. They do not seem to be directly related to the stipules because they are enclosed by the petiole. Catkins with both staminate and pistillate flowers are rare in S. interior, but a Quebec specimen had some catkins predominantly pistillate and others staminate; most were a mixture. The flowers were not teratological, but a mature capsule contained aborted ovules.

Hybrids:

Salix interior forms natural hybrids with S. exigua var. exigua. Controlled pollinations using S. interior (as S. exigua) from southern Ontario (A. Mosseler 1990) successfully produced F1 hybrids with S. bebbiana, S. discolor, S. eriocephala, and S. petiolaris. Seed production was usually relatively low, except in crosses with S. discolor. In general, F1 viability was relatively low in crosses with these members of subg. Vetrix. No seeds were produced in crosses with members of subgenera Protitea or Salix. Morphology of the hybrids usually was intermediate between the two parents, but when S. petiolaris was used as the maternal parent, the F1s more closely resembled that species. J. Salick and E. Pfeffer (1999) extended these findings to show that, although crosses between S. interior (as S. exigua) and S. eriocephala are partially sterile, their clonal growth parameters (sprouting, shoot length, and biomass production) are strong and thus permit these partially sterile hybrids to exist as successful individuals and perhaps to “... make a contribution to interspecific gene flow over time.” Of particular taxonomic interest is that, in this cross, the staminate parent has a significant influence on leaf shape, whereas in the cross S. eriocephala × S. petiolaris it is the pistillate parent that is significant for leaf shape. Relatively few hybrids resembling those produced by Mosseler have been recognized in nature, but it is possible that the unusually broadly leaved plants named S. interior var. exterior and var. wheeleri, from northern Maine, Nebraska, New York, and West Virginia, and probably elsewhere, may be hybrids. Phenological isolation may be strong enough to prevent crosses in nature (A. Mosseler and C. S. Papadopol 1989) with the earlier flowering S. eriocephala and S. petiolaris, a barrier that even an occasional period of overlap cannot breach.

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

The Virginia plants of Salix lucida are introduced (G. W. Argus 1986).

The Salix lucida complex is a group of three weakly delimited taxa, S. lasiandra var. caudata, S. lasiandra var. lasiandra, and S. lucida. The morphological characters used to separate them (leaves amphistomatous or hypostomatous and blades glaucous abaxially or not) are usually geographically correlated, but there are exceptions. G. W. Argus (1986b) proposed, based on principal components analysis of morphological data, to treat them as a single species consisting of three subspecies. The geographic overlap of the northeastern S. lucida and the western S. lasiandra is a relatively small area in central Saskatchewan. Evidence of intergradation was based on cultivation of a plant that, in the wild, had leaves that were not glaucous abaxially but were glaucous in cultivation. It seems best to treat them as two species, S. lucida and S. lasiandra, the latter with two varieties, var. lasiandra and var. caudata.

Hybrids:

Salix lucida forms natural hybrids with S. alba and S. nigra. Hybrids with S. serissima have been reported (M. L. Fernald 1950) but no convincing specimens have been seen. Attempts to hybridize S. lucida with members of subg. Protitea (S. amygdaloides), subg. Longifoliae (S. interior), and subg. Vetrix (S. discolor, S. eriocephala, and S. petiolaris) were unsuccessful (A. Mosseler 1990).

Salix lucida × S. nigra (S. ×schneideri B. Boivin) seems to be a rare intersubgeneric hybrid between tetraploid S. lucida and diploid S. nigra. It is known only from the type specimen, an infertile plant, growing with both parents. It resembles S. lucida in bud-scale margins connate, in petiolar glands stalked or foliaceous, and in leaf shape, and S. nigra in stipules rudimentary on proximal leaves and sometimes even on early leaves, stipule apex acute, pistillate catkins relatively long and slender, and styles relatively short.

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

Source FNA vol. 7, p. 56. FNA vol. 7, p. 46.
Parent taxa Salicaceae > Salix > subg. Longifoliae Salicaceae > Salix > subg. Salix > sect. Salicaster
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. 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
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. 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. rubra, S. exigua var. exterior, S. exigua subsp. interior, S. exigua var. pedicellata, S. exigua var. sericans, S. fluviatilis var. sericans, S. interior var. exterior, S. interior var. pedicellata, S. interior var. wheeleri, S. linearifolia, S. longifolia var. interior, S. longifolia var. pedicellata, S. longifolia var. sericans, S. longifolia var. wheeleri, S. wheeleri Pleiarina lucida, S. lucida var. angustifolia, S. lucida var. intonsa
Name authority Rowlee: Bull. Torrey Bot. Club 27: 253. (1900) Muhlenberg: Ges. Naturf. Freunde Berlin Neue Schriften 4: 239, plate 6, fig. 7. (1803)
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