Flora of North America species comparison

Of conservation concern.

Potentilla breweri differs from other members of sect. Multijugae in its often dense, cottony vestiture. Density of cottony hairs and leaflet dissection can differ significantly between first-formed and mid- to late-season leaves of P. breweri; in the description above, leaves are those predominant at anthesis.

Potentilla breweri is most common in the Sierra Nevada of California, with sporadic occurrences to the Cascade Range in southern Washington. Disjunct populations occur in the Ruby and Snake ranges in Nevada and on Steens Mountain in Oregon, where often introgressed with P. versicolor. Reports from Utah are based on collections of P. concinna var. proxima or possible hybrids between P. concinna var. proxima and P. ovina var. decurrens.

J. Clausen et al. (1940) concluded that Potentilla breweri (with P. versicolor as synonym) belonged with P. bruceae and P. drummondii as members of a cenospecies that probably also included unnamed species (possibly P. ovina var. decurrens) from the mountains of Colorado, Utah, and Wyoming. Chromosome number varied within populations, and high numbers of univalents were present.

Recognition of Potentilla breweri as a distinct species differs from recent treatments in which it was considered to be a variety or subspecies of P. drummondii, parallel to the treatment of P. bruceae. The present continental perspective of the genus, as well as additional fieldwork, has resulted in the return of all three to species rank (B. Ertter and D. Mansfield 2007). Placement of P. breweri in sect. Multijugae, separate from P. bruceae and P. drummondii in sect. Graciles, is based on the commonly prostrate habit, fully pinnate leaves, and deeply divided overlapping leaflets.

Although B. C. Johnston (1980) used Potentilla breweri var. viridis Jepson to accommodate greener-than-average sparsely cottony plants, including populations treated here as P. versicolor, the type is probably a sterile hybrid with P. wheeleri as one parent (B. Ertter 1992). The type of P. millefolia var. algida Jepson (included by Johnston in the synonymy of var. viridis) and comparable plants from north-central California combine features of P. breweri and P. versicolor but are more glandular than either. This variant, as well as exceptionally small plants from the Warner Mountains of California, may prove distinct.

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

Subspecies 4 or 5 (4 in the flora).

Potentilla anserina is polymorphic in most features, especially in hairiness, but also in size and in degree of dissection of leaflets, epicalyx bractlets, and sepals. While most of the variation described by A. G. Blytt (1906) is taxonomically insignificant, A. Rousi (1965) found support for three northern races: subspp. anserina, egedei, and pacifica. He also suggested that P. yukonensis Hultén might qualify as a separate subspecies. This treatment follows J. Soják (1994) in accepting four northern subspecies of P. anserina, all present in North America.

A. Rousi (1965) demonstrated partial interfertility between the races of Potentilla anserina, which form intermediates in all zones of contact. The distinctness of the four races, in spite of intermediates, is upheld by being partly allopatric and occupying different habitats where they are sympatric. As partly interfertile parapatric entities, they are best treated as subspecies.

The vast majority of chromosome counts are tetraploid. Tetraploid plants (2n = 28) are fully fertile; hexaploids (2n = 42) are largely pollen and seed sterile; pentaploids (2n = 35) are probably occasional hybrids (S. Erlandsson 1942, 1942b; A. Rousi 1965). A. Kurtto et al. (in J. Jalas et al. 1972+, vol. 13) considered numbers above tetraploid level as cases of occasional autopolyploidy.

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