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Habit Plants in compact hairy cushions, grayish green. Plants in loose tufts, olivaceous to black.
Stems

1–2 cm, central strand absent.

0.5–0.9 cm.

Leaves

ovate to oblong-lanceolate, 0.1–1.15 × 0.3–0.5 mm, keeled, not plicate, margins plane, awns 1–2 mm, very long, smooth to slightly denticulate, flattened basally, long-decurrent, costal transverse section prominent, semi-circular;

basal juxtacostal laminal cells rectangular, sometimes nodulose, thin- to thick-walled;

basal marginal laminal cells rectangular with thickened transverse walls, pellucid in 2–4 rows;

medial laminal cells rounded-quadrate, slightly sinuose, thick-walled;

distal laminal cells yellowish green, 1-stratose with 2-stratose ridges, not bulging, marginal cells 2-stratose, not bulging.

oblong-ovate to oblong-lanceolate, 1.6–2 × 0.3–0.6 mm, concave, awn 0.3–0.6 mm;

basal juxtacostal laminal cells quadrate to long-rectangular, straight, thin-walled;

basal marginal laminal cells quadrate to short-rectangular, straight, thin-walled;

medial laminal cells rounded, straight, thick-walled;

distal laminal cells 2-stratose, marginal cells 2-stratose.

Seta

sigmoid, 0.3–0.5 mm.

Sexual condition

dioicous, perichaetial leaves enlarged.

dioicous.

Capsule

absent in northern hemisphere material, emergent to shortly exserted, yellowish brown, oblate, exothecial cells irregularly short-rectangular, thin-walled, stomata absent, annulus of 1 row of quadrate, thick-walled cells, operculum mammillate to rostrate, peristome present, nearly fully-developed, split and perforated only in apex, papillose.]

usually present, exothecial cells thin-walled, annulus of 2–3 rows, rectangular, thick-walled, revoluble, operculum obliquely rostrate, peristome present, rudimentary, teeth composed of only a few rows of cells, perforated, papillose.

[seta straight, 1.5–2 mm.

Grimmia reflexidens

Grimmia crinitoleucophaea

Habitat Dry acidic rock Basalt, granite, schist and limestone
Elevation low [to moderate] elevations (50[-300] m) (low [to moderate] elevations (200[-1000] ft)) moderate to high elevations (500-2100 m) (moderate to high elevations (1600-6900 ft))
Distribution
from FNA
NF; South America (Argentina, Chile); Atlantic Islands (Iceland); Pacific Islands (New Zealand); Australia
from FNA
AZ; CA; CO; NM; NV; UT; WA; BC; NT; YT; Eurasia
Discussion

Of conservation concern.

Previous to its discovery in Iceland, as Grimmia grisea (H. C. Greven 1998), G. reflexidens was known from only the Southern Hemisphere. It had previously been collected east of East Bay, Newfoundland, now the only known locality in North America, but was not recognized as G. reflexidens. The latter is similar to G. asperitricha Dixon & Sainsbury of New Zealand, and the two species have been confused by G. O. K. Sainsbury (1945) as well as by R. Ochyra (1993). J. Muñoz (1998b) synonymized G. reflexidens with G. sessitana. However, the former is readily separated from the latter by: (1) enlarged perichaetial leaves, (2) decurrent awns, (3) non-bulging laminal cells, and (4) dioicous sexual condition. Capsules are unknown from Northern Hemisphere material, but G. reflexidens lacks stomata while they are present for G. sessitana. Although G. reflexidens and G. teretinervis both have decurrent awns they are easily separated by a number of characters: G. reflexidens grows in compact cushions, has long awns, and a semicircular costa; G. teretinervis grows in loose clumps, is hyaline-tipped to short-awned, and has a unique costa that is distally almost completely circular in transverse section.

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

In North America, Grimmia crinitoleucophaea is known from only scattered localities in the American west and in three extremely disjunct sites in Canada: in southern British Columbia, near the Keele River of the Northwest Territories, and along the Dempster Highway in the Yukon. It is found on a broad range of both basic and acidic rock types. Its subgeneric placement is problematic. Gametophytically the species is inseparable from G. tergestina, of subg. Litoneuron. Indeed, based on areolation and leaf shape, L. Loeske (1913–1914, part 1) placed it as a subspecies of the latter. This close similarity may account for reports by J. Muñoz and F. Pando (2000) and D. H. Norris and J. R. Shevock (2004) of G. tergestina from North America. We have seen all cited specimens in these papers and they all represent G. crinitoleucophaea or G. ovalis. Therefore, we reject G. tergestina being in North America. Sporophytic characters of G. crinitoleucophaea (a short, arcuate to sigmoid seta that is eccentrically attached to the capsule, an immersed ventricose capsule with a small, mitrate calyptra, and 3–4 large stomata) clearly indicate membership in subg. Grimmia. Further, G. crinitoleucophaea and G. tergestina have never been collected together, suggesting that the two are also ecologically distinct. Despite its dioicous sexuality, G. crinitoleucophaea is usually fertile; its rudimentary peristome and large annulus are thus readily evident. Its 2-stratose laminal stratification separates it from specimens of G. plagiopodia that may have broken peristome teeth.

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

Source FNA vol. 27, p. 238. FNA vol. 27, p. 232.
Parent taxa Grimmiaceae > subfam. Grimmioideae > Grimmia > subg. Guembelia Grimmiaceae > subfam. Grimmioideae > Grimmia > subg. Grimmia
Sibling taxa
G. alpestris, G. americana, G. anodon, G. anomala, G. arizonae, G. atrata, G. attenuata, G. brittoniae, G. caespiticia, G. crinitoleucophaea, G. donniana, G. elatior, G. elongata, G. funalis, G. hamulosa, G. hartmanii, G. incurva, G. laevigata, G. leibergii, G. lesherae, G. lisae, G. longirostris, G. mariniana, G. mollis, G. montana, G. moxleyi, G. muehlenbeckii, G. nevadensis, G. olneyi, G. orbicularis, G. ovalis, G. pilifera, G. plagiopodia, G. pulvinata, G. ramondii, G. serrana, G. sessitana, G. shastae, G. teretinervis, G. torquata, G. trichophylla, G. unicolor
G. alpestris, G. americana, G. anodon, G. anomala, G. arizonae, G. atrata, G. attenuata, G. brittoniae, G. caespiticia, G. donniana, G. elatior, G. elongata, G. funalis, G. hamulosa, G. hartmanii, G. incurva, G. laevigata, G. leibergii, G. lesherae, G. lisae, G. longirostris, G. mariniana, G. mollis, G. montana, G. moxleyi, G. muehlenbeckii, G. nevadensis, G. olneyi, G. orbicularis, G. ovalis, G. pilifera, G. plagiopodia, G. pulvinata, G. ramondii, G. reflexidens, G. serrana, G. sessitana, G. shastae, G. teretinervis, G. torquata, G. trichophylla, G. unicolor
Synonyms G. grisea
Name authority Müller Hal.: Syn. Musc. Frond. 1: 795. (1849) Cardot: Rev. Bryol. 17: 18. (1890)
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