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Published In: Die natürlichen Pflanzenfamilien, Zweite Auflage 10: 261. 1924. (Nat. Pflanzenfam. (ed. 2)) Name publication detail
 

Project Name Data (Last Modified On 11/3/2011)
Acceptance : Accepted
Project data     (Last Modified On 11/3/2011)
Nomenclature:

6. PSEUDOSYMBLEPHARIS            Plate 7.

Pseudosymblepharis Broth., Nat. Pfl. ed. 2, 10: 261, 1924. Lectotype: Pseudosymblepharis papillosula Card. & Thér. fide Saito, J. Hattori Bot. Lab. 39: 439, 1975.

Habitat:

            A genus found in most tropical and warm-temperate areas, occurring on soil, rock (mostly calcareous) and bark.

Notes:

            This genus is like both Tortella and Trichostomum subg. Oxystegus in the plane or broadly incurved leaf margins (Pl. 7, f. 20) and well differentiated, often inflated basal cells that usually extend up the margins in a more or less distinct vee (Pl. 7, f. 9, 18). The broadly sheathing leaf base with distinct “shoulders” has been used in the past as a major character, but is actually found to some extent in other genera, and is poorly or not at all developed in some species of Pseudosymblepharis. An additional and possibly better character is the relative size of the ventral stereid band (Pl. 7, f. 6, 20). In Pseudosymblepharis the ventral stereid band is almost always distinctly larger than the dorsal, and is often strongly bulging ventrally. Tortella may be additionally distinguished by the usually better developed peristome, while Trichostomum subg. Oxystegus differs, gametophytically, by the vee of basal cells poorly developed or absent. There may well prove to be no acceptable distinction between Pseudosymblepharis and Trichostomum subg. Oxystegus, excepting the color of the peristomes, yellow to white in the former and red in the latter (also see discussion of Norris and Koponen 1989). In leaf shape, P. indica might be recognized in Trichostomum subg. Oxystegus (cf. Hilpert 1933) but the costa is quite thick, with the ventral stereid band larger than the dorsal (at least in the larger, mature leaves). Problematically, T. (Oxystegus) hybernicus has the sheathing leaf base of Pseudosymblepharis and a ventral stereid band equal to or greater than the dorsal, but the rectangular upper laminal cells and thin-walled cells of the central cylinder associate it clearly with Trichostomum tenuirostris. The genus Pseudosymblepharis has considerable resemblance to Symblepharis Mont. (Dicranaceae), but gametophytes of the latter genus may be distinguished by their smooth leaf cells. The generitype of Trichostomum, T. brachydontium, has the ventral stereid band much larger than the dorsal in most very robust specimens, much as is the case in Pseudosymblepharis. Weissia jamaicensis has a leaf shape and costal structure similar to that of Pseudosymblepharis but the sharply and narrowly incurved upper laminal margins are characteristic only of Weissia s. lat. and Chionoloma. This entire relationship needs careful revision.

            Tortella has 32 filamentous teeth, longer than 500 µm, these strongly twisted. Trichostomum (including subgenus Oxystegus) has 16 teeth cleft variously to near that base, shorter than 400 µm, and straight to very weakly twisted. Future evaluation may find that Tortella and Trichostomum (s. lat.) may better be divided by characters other than those of the sporophyte and basal cell area shape of the leaves. A similar situation has occurred in the Barbula-Didymodon group, which was in the past distinguished along similar lines of peristome morphology, but which is now (Saito 1975a) separated into three genera (Bryoerythrophyllum being segregated from Didymodon) by a combination of several gametophytic characters (see treatments below).

            There may be quite a difference in stature between various collections of the same species, with certain variation correlated with plant size. In P. schimperiana, for instance, small plants may be only weakly sheathing at the leaf base, the hyaline basal cells of such collections may reach up the margins to half the length of the leaf, and the leaves are more commonly fragile. Examined collections of the widespread species Old World species P. angustata (holotype, NY!) are nearly identical to the New World P. schimperiana, but differ in lacking a stem central strand (weak in P. schimperiana). A revision of this genus, however, may yet demonstrate synonymy and a pan-tropical distribution of P. angustata.

Literature: Crum (1952a).
Number of accepted species: 11
Species Examined: P. angustifolia (MICH), P. angustata (BUF, NY), P. cavernarum (H), P. circinnatula (H), P. duriuscula (BUF, NY), P. indica (BM, NY), P. khasiana (NY), P. mauiensis (DUKE, NY), P. perlongifolia (NY), P. schimperiana (BUF, CANM, DUKE, NY, SPA, TENN), P. subduriuscula (BUF, NY), P. syrrhopodontoides (BM), P. verrucosa (H).

 

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     Plants growing in clumps or turf, green above, brown or reddish brown below. Stems branching often and irregularly, often long, to 2–4(–6) cm in length, transverse section rounded-pentagonal, central strand usually present, occasionally small, cells of central cylinder often thick-walled, sclerodermis usually weakly developed and composed of substereid cells, hyalodermis present, sturdy, collapsed only in very mature parts of stem; axillary hairs to 16 cells in length, all hyaline or basal 1–3 cells yellow; rhizoids sparse or stem occasionally weakly red-tomentose. Leaves incurved, contorted to spiralled when dry, spreading to squarrose from a usually sheathing base when moist, lanceolate to linear, 1–7 mm in length, upper lamina often narrow, flat to weakly tubulose, margins plane, entire or occasionally weakly dentate at apex, margins often eroded by fragmentation, occasionally decurrent; apex subulate, sharp, occasionally narrowly obtuse, often fragile and broken; base usually strongly sheathing, ovate to rectangular, with “shoulders”; costa excurrent as a sharp, cylindrical mucro or occasionally percurrent, superficial cells quadrate to short-rectangular, occasionally elongate near apex ventrally, elongate dorsally, (4–)8–15 rows of cells across costa ventrally at midleaf, costal transverse section semicircular to ovate, stereid bands strong, the dorsal usually larger than the ventral, epidermis ventrally present, dorsally present, weak or absent, guide cells (4–)6–9 in 1 (occasionally partially bistratose) layer, hydroid strand absent; upper laminal cells subquadrate to short-rectangular, 8–10 µm in width, 1(–2):1, walls evenly thickened, superficially weakly convex on both sides, occasionally strongly bulging ventrally and weakly convex dorsally; papillae bifid, 3–5 crowded over each lumen or fused into one capitulate papilla, or cells occasionally nearly smooth; differentiated basal cells filling leaf base, often reaching up margins in a vee, rectangular to bulging-rectangular, 13–25 µm in width, 3–5:1, walls thin, becoming thicker above, occasionally porose medially. Dioicous. Perichaetia terminal (these occasionally appear lateral because of subperichaetial elongate, overtopping branches), inner leaves little different from cauline leaves or high-sheathing. Perigonia terminal, inner leaves little different from the cauline leaves. Seta 0.7–2.0 cm in length, 1 per perichaetium, brown to reddish brown, twisted clockwise below, counterclockwise above; theca (0.5–)2.0–2.5 mm in length, reddish brown, cylindrical, exothecial cells rectangular, 20–30 µm in width, 2–4:1, walls thin, stomates present at base of theca, phaneropore, annulus usually of 2–4 rows of vesiculose cells, deciduous in pieces; peristome teeth 16, rather short, occasionally absent, yellow to whitish, triangular to linear, cleft and perforated to near base, spiculose, 125–300 µm in length, with many articulations, straight, basal membrane when present 35–50 µm in height, spiculose. Operculum rostrate, (0.4–)1.2 mm in length, cells straight. Calyptra cucullate, smooth, ca. 2 mm in length. Spores 11–15 µm in diameter, yellow-brown, papillose. Laminal KOH color reaction golden yellow-orange, occasionally deep yellow. Reported chromosome number n = 13, 14.

 
 
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