Sphagnum lindbergii |
Sphagnum isoviitae |
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brown-stem peat-moss, Lindberg's sphagnum |
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Habit | Plants moderate-sized to large, moderately densely branched; green to brown, often bluish tinged and/or shiny when dry; capitulum flattopped with a conspicuous terminal bud. | Plants moderate-sized and moderately weak-stemmed to moderately stiff; green, brownish green to brown; capitulum flat-topped and 5-radiate, terminal bud often visible. |
Stem(s) | leaves lingulate-spatulate, large, 1.3–1.6 mm; appressed to stem; apex very broad and lacerate; hyaline cells efibrillose and aporose, often septate. |
leaves triangular to lingulate-triangular, equal to or more than 0.8 mm, spreading to appressed; apex acute to apiculate, hyaline cells mostly efibrillose and nonseptate. |
Branches | strongly 5-ranked and straight. |
± straight and somewhat tapered, usually 5-ranked, leaves not greatly elongated at branch distal end. |
Branch leaves | ovate-lanceolate, 1.5–3 mm; straight to slightly subsecund; imbricate to somewhat reflexed and not undulate; margins entire; hyaline cells long and narrow, length to width ca. 10:1 on convex surface with 1 or more small pores in the cell ends and angles and often with numerous pseudopores along the margins, on concave surface with large round wall thinnings on the cell ends and angles; chlorophyllous cells triangular to trapezoidal in transverse section, apex often exposed on concave surface. |
narrowly ovate-lanceolate, greater than 1.2 mm, straight, slightly undulate and weakly recurved when dry, margins entire; hyaline cells on convex surface with 1 pore per cell in apical end, on concave surface with round wall thinnings in the cell ends and angles; chlorophyllous cells in transverse section triangular to ovate-triangular and well-enclosed on the concave surface. |
Sexual condition | monoicous or dioicous. |
dioicous. |
Spores | 22–34 µm; both surfaces smooth, apparent ridged border on proximal surface; proximal laesura more than 0.5 spore radius. |
24–33 µm; finely papillose on the superficial surface. |
Branch | fascicles with 2 spreading and 2 pendent branches, leaves not much elongated at distal end.; branch stems green, with cortex enlarged with retort cells. |
fascicles with 2 spreading and 2–3 pendent branches.; branch stems green and often reddish at proximal end, with cortex enlarged with conspicuous retort cells. |
Sphagnum lindbergii |
Sphagnum isoviitae |
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Habitat | Widespread forming carpets in ombrotrophic to weakly minerotrophic boreal mires | Forming carpets in a wide variety of poor to medium fen habitats of both mire edge and mire wide character, not found in ombrotrophic mires |
Elevation | low to high elevations | low to moderate elevations |
Distribution |
AK; CO; NH; NY; WA; AB; BC; MB; NF; NS; NT; NU; ON; QC; YT; Greenland; Eurasia |
CT; IN; MA; MD; ME; MI; MN; NC; NH; NJ; NY; OH; PA; VA; VT; WV; AB; NF; NS; QC; Europe |
Discussion | Sporophytes are uncommon. Sphagnum lindbergii is normally easily distinguished from other carpet-forming species of sect. Cuspidata by its large, strongly lacerate stem leaf and dark brown to black stem. Sexual condition is taken from from L. I. Savicz-Lubitzkaya and Z. N. Smirnova (1968). (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Sporophytes are uncommon in Sphagnum isoviitae. See discussion under 26. S. brevifolium and 28. S. fallax for distinction from these similar species. Sphagnum isoviitae has no range overlap with S. pacificum, the other North American species of the S. recurvum complex with apiculate stem leaves; the sharply recurved branch leaves of the latter, however, would separate it easily in any case. Spore features are those given by Flatberg. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Source | FNA vol. 27, p. 70. | FNA vol. 27, p. 68. |
Parent taxa | Sphagnaceae > Sphagnum > sect. Cuspidata | Sphagnaceae > Sphagnum > sect. Cuspidata |
Sibling taxa | ||
Name authority | Schimper: Öfvers. Kongl. Vetensk.-Akad. Förh. 14: 126. (1857) | Flatberg: J. Bryol. 17: 2, figs. 1, 2. (1992) |
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