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slender Russian-thistle, slender saltwort, tumbleweed

barbwire Russian-thistle, Paulsen's Russian thistle

Habit Herbs, 10–100 cm, sparsely to densely papillose or hispid (rarely subglabrous). Herbs, 10–80(–100) cm, glabrous or sparsely papillose to hispid.
Stems

erect, rarely ascending, branched above base (occasionally with slender branches near base);

branches straight or slightly arcuate.

erect, rarely ascending or prostrate, profusely branched from or near base (rarely simple in underdeveloped specimens);

branches straight or arcuate.

Leaves

alternate;

blade filiform to narrowly linear, 1–2 mm wide, less than 1 mm wide in herbarium specimens, usually not fleshy, sometimes semi-amplexicaul at base, apex with soft bristle (rarely subspinescent).

alternate;

blade filiform to narrowly linear, usually less than 1 mm wide, occasionally to 2 mm wide in herbarium specimens, fleshy or not, not swollen at base, apex subspinose or spinescent.

Inflorescences

not interrupted, dense, 1-flowered (rarely 2–3-flowered), often also in axils of proximal leaves and branches, lower ones tightly enclosed in bracts and bracteoles, forming gall-like caducous balls at maturity;

bracts alternate, strongly imbricate and appressed at maturity, base not distinctly swollen, apex acuminate into subulate spine.

distinctly interrupted at maturity, 1-flowered (rarely 2–3-flowered with lateral flowers mostly abortive);

bracts alternate, not imbricate, strongly reflexed at maturity, base not distinctly swollen, narrowing into spinose apex.

Flowers

bracteoles becoming connate basally and adnate to perianth segments;

perianth segments wingless or with narrow, erose wing at maturity, apex acute, weak and flaccid, glabrous; fruiting perianth ca. 2–5 mm diam. 2n = 18.

bracteoles spreading or reflexed, distinct or connate near base, spinescent;

perianth segments prominently winged (two wings usually reduced to small, almost subulate winglike appendages), apex long-acuminate or long-subulate and spinose, forming slender columnar beak distal to wings at maturity, glabrous; fruiting perianth 7–12 mm diam. 2n = 36.

Salsola collina

Salsola paulsenii

Phenology Fruiting summer–fall. Flowering spring–summer.
Habitat Waste places, roadsides, railway areas, cultivated fields, disturbed natural and seminatural plant communities Sandy soils, disturbed natural and seminatural plant communities, semideserts, deserts, eroded slopes, sand dunes, sandy waste places
Elevation 100-2000 m (300-6600 ft) 0-1900 m (0-6200 ft)
Distribution
from FNA
AZ; CO; IA; KS; KY; MI; MN; MO; MT; ND; NE; NH; NM; NY; OK; SD; UT; VT; ON; SK; Eurasia [Introduced in North America]
[WildflowerSearch map]
[BONAP county map]
from FNA
AZ; CA; CO; NV; UT; se Europe; c Asia [Introduced in North America]
[WildflowerSearch map]
[BONAP county map]
Discussion

Salsola collina was reported for the first time for North America from Minnesota by J. W. Moore (1938). It was collected in Kansas in 1923 (R. E. Brooks et al. 1976), but misidentified. Later it was discovered in Colorado, Iowa, and Missouri (V. L. Cory 1948; W. Schapaugh 1958; V. Muhlenbach 1979). Reports of S. collina for Arizona and New York are based on specimens cited by S. Rilke (1999). Its actual distribution seems to be underestimated due to the common and constant confusion with deviant forms of S. tragus. In the future, S. collina may be expected to occur within the major portion of the present range of S. tragus.

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

Salsola paulsenii may be expected in the future also in New Mexico and Texas, as well as in some Great Plains states. It was first reported from North America by P. A. Munz (1968). Additional details of distribution and morphology of this species have been discussed by J. C. Beatley (1973c), T. C. Fuller (1986), and S. Rilke (1999).

Salsola paulsenii is weakly differentiated from S. tragus sensu stricto. Intermediate forms between them seem to be more common along margins of the natural range of the species and in secondary, synanthropic localities. According to S. Rilke (1999), the hybrids S. paulsenii × S. tragus are identical with S. ×gobicola Iljin. Forms conventionally named as “Salsola X” and “S. paulsenii lax form” with 2n = 54 (H. L. Arnold 1972; F. J. Ryan and D. R. Ayres 2000) are probably also of hybrid origin.

Reports of chromosome number 2n = 18 for Salsola paulsenii are probably erroneous and based on misinterpretation of data provided by N. L. Semiotrocheva (1983).

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

Source FNA vol. 4, p. 402. FNA vol. 4, p. 402.
Parent taxa Chenopodiaceae > Salsola Chenopodiaceae > Salsola
Sibling taxa
S. kali, S. paulsenii, S. soda, S. tragus, S. vermiculata
S. collina, S. kali, S. soda, S. tragus, S. vermiculata
Name authority Pallas: Ill. Pl., 34. (1803) Litvinov: Izv. Turkestansk. Otd. Imp. Russk. Geogr. Obshch. 4(5): 28. (1905)
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