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sandbar willow

Bonpland willow, Bonpland's willow, red willow

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. Trees, 1–13 m. Stems: branches yellow-brown to red-brown, glabrous; branchlets yellowish, streaked with red or red-brown, glabrous or puberulent, nodes hairy.
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.

(marcescent), stipules absent or rudimentary on early ones, foliaceous on late ones, apex rounded, convex, or acute;

petiole (rarely with spherical glands distally), 4–16 mm, puberulent or pubescent to glabrescent adaxially;

largest medial blade lorate to narrowly lanceolate, 58–155 × 7–27 mm, 4.5–10.7 times as long as wide, base cuneate to convex, margins serrulate to crenulate or entire, apex acuminate to acute, abaxial surface glabrous or glabrescent, hairs appressed, adaxial dull or slightly glossy, glabrous or pilose;

proximal blade margins entire;

juvenile blade glabrous, puberulent, pilose, or sparsely long-silky abaxially, hairs white.

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 0.2–0.6 mm, adaxial nectary oblong, square, or ovate, 0.2–0.6 mm, nectaries distinct or connate and cup-shaped;

stamens 3–7;

filaments hairy basally;

anthers 0.3–0.5 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 to oblong, 0.3–0.6 mm;

stipe 0.4–2.4 mm;

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

ovules 8–18 per ovary;

styles 0.2–0.3 mm;

stigmas (sometimes slenderly cylindrical), 0.18–0.27–0.32 mm.

Capsules

(4–)5–8(–10) mm.

3–6 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.

(usually flowering throughout season and axillary, sessile), staminate 24–131 × 3–10 mm, flowering branchlet 0–12 mm; pistillate (densely to loosely flowered), 24–47 × 6–12 mm, flowering branchlet 0–10 mm;

floral bract 0.6–2.2 mm, apex rounded to convex, irregularly toothed or entire, abaxially sparsely to moderately densely hairy proximally, hairs irregularly curly; pistillate bract persistent after flowering.

2n

= 38.

= 38.

Salix interior

Salix bonplandiana

Phenology Flowering early Apr-early Jul. Flowering Feb–Apr and throughout year.
Habitat Sandy to silty flood plains, margins of lakes, ponds, and prairie sloughs, dry prairie sand hills, marshes, disturbed areas Riparian forests, along streams, dry washes
Elevation 10-1800 m (0-5900 ft) 700-2000 m (2300-6600 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
AZ; Mexico (Baja California, Chiapas, Chihuahua, Distrito Federal, Durango, Guanajuato, Guerrero, Hidalgo, Jalisco, Michoacán, Morelos, Nuevo León, Oaxaca, Puebla, Querétaro, Sonora, Tlaxcala, Veracruz, Zacatecas); Central America (Guatemala)
[WildflowerSearch map]
[BONAP county map]
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.)

Salix bonplandiana and S. laevigata are closely related and are sometimes treated as varieties (R. D. Dorn 1994). Their ranges overlap in Arizona and in northern Baja California, Mexico.

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

Source FNA vol. 7, p. 56. FNA vol. 7, p. 33.
Parent taxa Salicaceae > Salix > subg. Longifoliae Salicaceae > Salix > subg. Protitea > sect. Humboldtianae
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. 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. 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 S. bonplandiana var. toumeyi
Name authority Rowlee: Bull. Torrey Bot. Club 27: 253. (1900) Kunth: in A. von Humboldt et al., Nov. Gen. Sp. 2(qto.): 24: plates 101, 102. (1817)
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