Sphagnum bartlettianum |
Sphagnum |
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Bartlett's sphagnum |
sphagnum |
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Habit | Plants ± moderate-sized, capitula flat-topped and stellate to some-what hemispherical; variegated pale yellowish and red, sometimes partially green or completely red; without metallic lustre when dry. | Plants typically with upright stems, young branches arranged spirally around stem at growing apex into a capitulum, branches clustered into fascicles along stem, stem and branch leaves of alternating inflated, S-shaped to rhomboid hyaline cells and narrow linear chlorophyllous cells, hyaline cells typically fibrillose and porose on branch leaves. | ||||||||||||||||||||||||||||||||||||
Stem(s) | leaves narrowly lingulate-triangular, 1.2–1.8 mm, apex acute to apiculate, border not developed much along margins and narrow at base (occupying less than 0.25 the width of the base); hyaline cells rhombic, mostly 0–1-septate. |
leaves may be less fibrillose or efibrillose and less porose or aporose than the branch leaves, often septate, a distinct border of narrow linear chlorophyllous cells often along margins and at base, and with a greater width:length ratio than branch leaves in anisophyllous forms, partly differentiated in hemiisophyllous forms, and identical in isophyllous forms. |
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Branches | usually strongly 5-ranked. |
typically dimorphic as spreading and pendent branches, but some species lack branches or branches are not clearly differentiated, pendent branches typically more slender than spreading branches and with a tendency to adhere to and cover the stem. |
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Branch leaves | narrowly ovate-lanceolate, 1.2–1.5 mm, concave, straight, apex strongly involute, border entire, hyaline cells on convex surface with 3–9 faintly ringed rounded-elliptic pores along the commissures often quite small apically, largely aporose on concave surface. |
with 2/5 phyllotaxy, of a 1-stratose network of alternating chlorophyllous and hyaline cells; hyaline cells usually S-shaped, rarely rhomboid, nearly always strengthened with conspicuous spiral fibrils, small to large, round to elliptic and sometimes ringed pores occur along commissures or rarely on cell lumen, convex surface typically with more pores per cell than concave surface; chlorophyllous cells may be enclosed on both surfaces, more broadly exposed on one surface or equally exposed on both surfaces as viewed in transverse section, adjacent cell walls typically smooth, but various types of cell wall projections may be clearly visible in transverse section. |
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Sexual condition | dioicous. |
dioicous or monoicous; stalked globose antheridia borne at the tips of branches usually with swollen colored tips of branches near capitulum; long-necked archegonia borne on short branches singly surrounded by perichaetial leaves that are typically longer than branch leaves. |
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Capsule | spherical, brown to black, lacking an annulus or peristome with a operculum convex; spore sac amphithecial in origin, over-arching columella. |
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Calyptra | membranous. |
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Spores | 19–28 µm; coarsely papillose on both surfaces with a distinct ridged border around perimeter of proximal surface; proximal laesura less than 0.5 spore radius. |
tetrahedral, with prominent trilete mark, fine to coarse superficial surface, distal surface may have raised Y-mark, bifurcated Y-mark sculpture, or none. |
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Branch | fascicles with 2 spreading and 1–2 pendent branches. |
fascicles typically with 2 spreading and 1–2 pendent branches, but there may be up to 12(–14) per fascicle.; branch stems typically green, with a superficial layer of inflated retort cells; these grouped or solitary, usually porose at the distal end with a conspicuous or inconspicuous neck. |
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Protonema | typically 1-stratose, gametophyte developing from lateral margin. |
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Sphagnum bartlettianum |
Sphagnum |
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Phenology | Capsules mature late spring to early summer. | |||||||||||||||||||||||||||||||||||||
Habitat | Ecology poorly understood, more southern weakly minerotrophic sites such as the mires in the Pine Barrens of N.J. and the pocosins of the Atlantic coastal plain | |||||||||||||||||||||||||||||||||||||
Elevation | low to moderate elevations | |||||||||||||||||||||||||||||||||||||
Distribution |
AK; AL; AR; CA; CT; DE; FL; IL; IN; KY; MA; MD; ME; MO; MS; NC; NH; NJ; NY; OH; OR; PA; RI; SC; TN; VA; VT; WI; WV; BC; NB; NF; NS; QC; Europe |
Worldwide except Antarctica; primarily in boreal regions but also in cool; moist montane and oceanic habitats such as nutrient-poor and acidic wetlands and mires |
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Discussion | Sporophytes are not common in Sphagnum bartlettianum. Confusion is most likely with S. rubellum, with which it frequently co-occurs in the northern part of its range. The ecology is poorly understood due to taxonomic confusion with S. rubellum; the latter species, however, is more typical of boreal poor fens and bogs. Sphagnum bartlettianum has a narrower stem leaf with a distinctly pointed and even apiculate tip, whereas the stem leaf on S. rubellum is quite rounded. The branch leaves of S. bartlettianum are also narrower than those of S. rubellum and are never subsecund as in the latter. Sphagnum quinquefarium has shorter and wider stem leaves as well as often having 3 spreading branches per fascicle. Sphagnum wilfii can appear quite similar and it does overlap the range of S. bartlettianum in coastal British Columbia and southeastern Alaska. Sphagnum wilfii has a stem leaf that is triangular to triangular-lingulate in contrast to the narrowly lingulate-triangular stem leaf of S. bartlettianum. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
Species 285 (89 in the flora). The concept of species in Sphagnum is controversial. We have followed P. Isoviita (1966) and K. I. Flatberg (1994) in the recognition of species. H. A. Crum (1984) and others (R. E. Daniels and A. Eddy 1985; A. L. Andrews 1958, 1959) have adopted more conservative taxonomic concepts for species in the Northern Hemisphere. Description of the spores above is from Cao T. and D. H. Vitt (1986); for additional discussion of the protonema see C. B. McQueen (1988). Microscopic features can be observed by using a concentrated aqueous or alcohol solution of Crystal Violet. A 50% solution of alcohol and Methylene Blue or Safranin Red can be used, but these usually do not stain features such as minute pores, fibrils, wall thinnings, and surface sculpture on the chlorophyllous cells. The number and kinds of branches should be determined, individual stem and branch leaves (from the middle of a spreading branch) should be examined from the distal 2 cm of the plant, and the superficial surface of stem cortical cells as well as cross sections of branch leaves and stems may need examination. (Discussion copyrighted by Flora of North America; reprinted with permission.) |
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Key |
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Source | FNA vol. 27, p. 90. | FNA vol. 27. | ||||||||||||||||||||||||||||||||||||
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Synonyms | S. bartlettianum var. roseum | |||||||||||||||||||||||||||||||||||||
Name authority | Warnstorf: in H. G. A. Engler, Pflanzenr. 51[III]: 105. (1911) | Linnaeus: Sp. Pl. 2: 1106. (1753): Gen. Pl. ed. 5, 487. 1754 , | ||||||||||||||||||||||||||||||||||||
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