Flora of North America species comparison

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 farriae is a cordilleran species ranging from Wyoming to central British Columbia with disjunct occurrences in northwestern British Columbia, western Northwest Territories, and southern Yukon. It is related to S. hastata, an amphiberingian species ranging from Scandinavia to southwestern Yukon and northwestern Northwest Territories. There may be reasons for treating these slightly different plants as S. hastata var. farriae, but R. D. Dorn (1975) maintained them as a species based on flavonoid differences. In a phenetic study (G. W. Argus 2007), the two taxa had dissimilarity values at the same level as other closely related species. They are treated here as species, primarily because their ranges are disjunct. They can be separated as follows:

Salix farriae is distinguished from S. hastata by having largest medial blades narrowly elliptic to elliptic, pistillate nectaries oblong or ovate, stipules on early leaves absent or rudimentary (sometimes foliaceous), branches strongly to weakly glaucous or not, floral bract apices rounded, and plants of the cordillera in Alberta and British Columbia, in Idaho, Montana, Oregon, and Wyoming; S. hastata has largest medial blades narrowly elliptic to broadly elliptic or broadly obovate, pistillate nectaries square, stipules on early leaves foliaceous (sometimes rudimentary), branches not glaucous, floral bract apices acute or rounded, and plants of Alaska, Northwest Territories, and Yukon.

Salix farriae and S. barclayi are sympatric in western Canada and the Pacific Northwest, where they are difficult to separate. Salix farriae can often be recognized by its largest medial leaves with at least some minute, ferruginous hairs on the adaxial midrib or blade surfaces; ferruginous hairs do not occur in S. barclayi. Its leaf margins also tend to be more nearly entire, but relatively short teeth are not infrequent. Such plants are sometimes interpreted as intergrades between S. farriae and S. barclayi (R. D. Dorn 1975). The variable leaf toothing also occurs in S. hastata and may not be a reliable indicator of intergradation. Salix farriae also differs from S. barclayi in usually having shorter anthers, 0.3–0.6 mm versus 0.6–1 mm in S. barclayi. See 61. S. barclayi.

Hybrids:

Salix farriae forms natural hybrids with S. barclayi.

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