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controverial weissia moss, green-cushion weissia moss, green-tuft stubble-moss, pigtail moss

weissia moss

Habit Plants in low cushions or turfs or loosely cespitose, green distally, brown to tan or yellow proximally.
Stems

to 1 cm, hyalodermis weakly differentiated to distinct, seldom absent, sclerodermis weakly differentiated in 1–2 layers, central strand present;

axillary hairs with proximal 1–2 cells somewhat thicker walled.

Leaves

short- to long-lanceolate, base weakly differentiated to ovate, shoulders weak or absent, distal laminal margins strongly and usually but not always sharply incurved or inrolled, apex plane to channeled, acute, mucro usually weak, of 1–5(–8) cells;

costal adaxial stereid band smaller than the abaxial;

distal laminal cells 6–13 µm wide.

incurved, commonly tubulose and often contorted or spiraled when dry, spreading when moist; long-ligulate, oblong or triangular to long-lanceolate, 1.5–2.5(–4) mm;

adaxial surface broadly channeled across leaf;

base scarcely differentiated to ovate or rectangular, occasionally half-sheathing;

distal margins usually sharply incurved, occasionally merely erect, seldom plane, entire;

apex sharply acute to subulate, occasionally broadly acute, obtuse, or weakly cucullate;

costa shortly and sharply mucronate, adaxial outgrowths absent, adaxial cells quadrate to short-rectangular except occasionally elongate near apex, in 4–8 rows;

transverse section ovate, occasionally circular or semicircular, adaxial epidermis present, adaxial stereid band present, guide cells 4–6(–8) in 1 layer, hydroid strand absent, abaxial stereid band present, crescent in sectional shape, abaxial epidermis present or occasionally absent;

basal cells differentiated across leaf, rarely rising higher along margins in a V shape, rectangular, occasionally rhomboid, 2–5:1;

distal medial cells subquadrate to hexagonal, 7–13 µm, papillae 2-fid, 2–6 per lumen, occasionally fused into a large multiplex papilla covering the lumen, occasionally spiculiform and branching.

Seta

elongate, 0.3–0.8 cm.

0.1–1.3 cm.

Sexual condition

monoicous.

monoicous (usually autoicous), occasionally dioicous;

perichaetia terminal, interior leaves occasionally sheathing seta, little different from cauline leaves or somewhat larger.

Capsule

stegocarpic, long-ovate to cylindric, operculum differentiated, falling, peristome present, teeth rudimentary to lanceolate, or occasionally absent.

stegocarpic or cleistocarpic; theca elliptical to short-ovate or cylindric, 1–2.2 mm, annulus in ca. 2 rows of persistent, vesiculose cells or not differentiated;

operculum when present conic to rostrate;

peristome teeth 16 or rudimentary or absent, occasionally removed with operculum, oblong-truncate to long-triangular, often irregularly cleft, straight or twisted weakly counterclockwise, mouth occasionally closed by a remnant of the spore sac.

Calyptra

cucullate.

Spores

14–28 µm.

Specialized

asexual reproduction rare, as rhizoidal gemmae.

Koh

laminal color reaction yellow.

Weissia controversa

Weissia

Phenology Capsules mature throughout year depending on area of the flora.
Habitat Weedy, soil, rock, disturbed areas, roadsides, fields, acid or calcareous substrates
Distribution
from FNA
AK; AL; AZ; CA; CO; FL; GA; IA; ID; IL; KS; KY; LA; MA; MI; MT; NC; NH; NJ; NM; NV; NY; OH; OK; OR; TN; TX; UT; VA; WA; WI; AB; BC; MB; NB; NL; NS; NT; ON; PE; QC; SK; YT; Mexico; Central America; South America; Africa; Pacific Islands; Greenland; Eurasia; West Indies; Australia
[WildflowerSearch map]
from USDA
Worldwide except Antarctica; found mostly on soil
Discussion

This treatment of Weissia controversa follows the study of A. Stoneburner (1985), which justifiably included W. andrewsii, and, agreeing with H. A. Crum and L. E. Anderson (1981), pointed out the great variation in peristome development including occurrence of both eperistomate and peristomate capsules in the same collection. The present treatment includes all flora area reports of W. condensa, a morphologically distinct European species with characters as listed in Excluded Species. Rhizoidal gemmae were reported by W. D. Reese (1988) but these are apparently rare. Weissia viridula Bridel is an illegitimate name that has been much used for this taxon.

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

Species ca. 97 (10 in the flora).

A world evaluation of Weissia and Trichostomum (R. H. Zander 1993) at the generic level suggested that species of the two genera might be shuffled into a more natural arrangement if taxa with identical or nearly identical gametophytes were grouped, with differences in sporophytes easily and simply explained by reduction. It is insufficient, however, to simply split Weissia and Trichostomum into two genera, as was implemented by Zander, based on leaf margins sharply incurved or erect to nearly plane, respectively. Weissia jamaicensis and T. crispulum have similar gametophytes but differ markedly in the leaves of the former being sharply incurved marginally and of the latter nearly plane to merely erect. No major changes were made, however, for this treatment given the need for a full revision. Certain Weissia species with erect leaf margins may have a somewhat cucullate leaf apex similar to that of T. crispulum, but the lamina of the latter is generally broader, 16–20 cells across on one side of the costa just above mid leaf (except in strongly reduced specimens with short-ovate leaves), while Weissia species with which it may be confused have laminae usually 10–15 cells across a lateral lamina. The present species concepts are largely identical with those of A. Stoneburner (1985) with exceptions as noted.

All species of Weissia with sharply inflexed distal leaf margins have a tendency to show adaxially bulging cells in leaf section, possibly because the inflexion crowds the cells. This differential bulging of cell superfices is probably homoplastic to adaxially bulging distal laminal cells in other pottiaceous genera without sharply inflexed distal margins, such as Hyophila. Thus, the close relationship of Weissia with Hyophila and relatives cladistically demonstrated by R. H. Zander (1993) is probably an artifact. Regarding the hymenium that may be seen closing the newly deoperculate capsules of the eperistomate segregate genus Hymenostomum, such a membrane is present in all species of the genus, being the top of the spore sac, and it is simply more evident in the eperistomate species.

Excluded Species:

Weissia condensa (Voit) Lindberg

This name replaces Weissia tortilis (Schwägrichen) Müller Hal., an illegitimate homonym according to M. F. V. Corley et al. (1981). Synonyms of this European species have been applied to specimens of W. controversa from the flora area include Hymenostomum tortile (Schwägrichen) Bruch & Schimper; W. euteiches R. H. Zander, superfluous name; and W. tortilis (Schwägrichen) Müller Hal., illegitimate homonym. European specimens of W. condensa usually have cucullate leaf apices, thick costae to 100 µm wide basally, distal laminal cells 8–10 µm wide, and capsules usually eperistomate; the leaves commonly have rather stout and long mucros of (4–)7–10 cells. Weissia sharpii is similar but has large distal laminal cells, 10–13 µm wide (2–)1:1. The combination of a strong mucro, wide costa and generally eperistomate but stegocarpic capsule is not found in the flora area and thus this species is excluded. Although A. Stoneburner (1985) attributed an eperistomate condition to W. condensa, R. H. Zander (1994h) pointed out that W. condensa may occasionally have a very rudimentary peristome, one or two segments high, hidden below the capsule stomal rim (e.g., Slovakia, Pilous 139, MO). The thickness of the capsule wall in numbers of cell layers was used by Zander to distinguish W. condensa from W. controversa in Mexico, but this is apparently not a good feature because all Weissia capsules examined in the present study are three to four cell layers thick although W. controversa occasionally has 2–3 layers, with the innermost layer difficult to demonstrate or possibly eroded or resorbed.

Weissia flavescens. E. Britton (= Trichostomum brittonianum R. H. Zander)

This species was reported from Florida by W. D. Reese (1991), but those sterile plants proved to be indistinguishable from Trichostomum crispulum.

Weissia wimmeriana (Sendtner) Bruch & Schimper

This is a European species whose report from Minnesota, according to A. L. Andrews (1933) was based on material of Weissia controversa.

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

Key
1. Leaves cucullate, base usually abruptly broadened, with prominent shoulders; costa with adaxial stereid band almost as large as or larger than the abaxial.
W. jamaicensis
1. Leaves with channeled or plane apex, base weakly or gradually broadened, lacking distinct shoulders; costa with adaxial stereid band clearly smaller than the abaxial
→ 2
2. Capsule stegocarpic, operculum falling, peristome present, often rudimentary, or absent
→ 3
2. Capsule cleistocarpic or at least indehiscent (operculum persistent), rarely fragments of peristome visible in transmitted light
→ 6
3. Laminal margins erect or almost plane, occasionally very broadly incurved, mucro strong and often cylindric, of 5-7(-10) cells.
W. brachycarpa
3. Laminal margins distally incurved (occasionally involute or rolled), mucro weak or strong, triangular, of 1-5(-9) cells
→ 4
4. Leaves long-elliptic or ligulate, base little wider than distal lamina, apex rounded- acute
W. ligulifolia
4. Leaves lanceolate to deltoid or ovate, base usually ovate or elliptic, apex acute to narrowly acute
→ 5
5. Leaves short- to long-lanceolate or linear, distal laminal cells 6-13 µm wide, margins distally strongly and usually but not always sharply incurved or inrolled.
W. controversa
5. Leaves deltoid to ovate, distal laminal cells 10-13 µm wide, distal margins usually loosely inrolled.
W. sharpii
6. Leaves short-lanceolate to elliptic, leaf mucro weak or strong, of 1-7 cells
→ 7
6. Leaves long-lanceolate, leaf mucro commonly strong, of (1-)3-7(-14) cells
→ 8
7. Mucro usually weak, of 1-3 cells; capsule ovoid-elliptic, seta 0.1-0.2 cm; leaves sharply inrolled on margins distally.
W. occidentalis
7. Mucro strong, of (3-)4-6(-7) cells; capsule ovoid to short-cylindric, seta 0.2- 0.3 cm; leaves plane to concave, margins seldom distinctly incurved.
W. inoperculata
8. Laminal margins distally strongly and sharply incurved or inrolled; operculum persistent, peristome absent or rudimentary.
W. phascopsis
8. Laminal margins erect or almost plane, occasionally very broadly incurved; operculum not differentiated, peristome absent
→ 9
9. Seta usually 0.08-0.15 cm, rhizautoicous, capsule with stomates.
W. ludoviciana
9. Seta less than 0.05 cm, cladautoicous, capsule lacking stomates.
W. muhlenbergiana
Source FNA vol. 27, p. 514. FNA vol. 27, p. 512. Author: Richard H. Zander.
Parent taxa Pottiaceae > subfam. Trichostomoideae > Weissia Pottiaceae > subfam. Trichostomoideae
Sibling taxa
W. brachycarpa, W. inoperculata, W. jamaicensis, W. ligulifolia, W. ludoviciana, W. muhlenbergiana, W. occidentalis, W. phascopsis, W. sharpii
Subordinate taxa
W. brachycarpa, W. controversa, W. inoperculata, W. jamaicensis, W. ligulifolia, W. ludoviciana, W. muhlenbergiana, W. occidentalis, W. phascopsis, W. sharpii
Synonyms Gymnostomum rauanum, Mollia viridula, W. andrewsii, W. brandegeei, W. controversa var. australis, W. controversa var. longiseta, W. controversa var. wolffii, W. curvicaulis, W. longiseta, W. microodonta, W. viridula var. nitida, W. wolfii Astomum, Hymenostomum, W. section Astomum, W. subg. Astomum, W. subg. Hymenostomum
Name authority Hedwig: Sp. Musc. Frond., 67. (1801) Hedwig: Sp. Musc. Frond., 64. 1801 ,
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