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Appalachian bristle fern, Appalachian filmy fern

scale-edge bristle fern

Habit Plants on rock. Plants epiphytic, on rock, or terrestrial.
Stems

long-creeping, slender, bearing widely spaced leaves;

stems covered with dark multicellular hairs of 2 kinds, unbranched gland-tipped hairs and branched or unbranched rhizoidlike hairs, sparsely rooted.

long-creeping, threadlike, bearing scattered leaves, covered with dark hairs of 2 types, multicellular gland-tipped hairs and elongate rhizoidlike hairs.

Gemmae

composed of short filaments of undifferentiated cells.

Leaves

lanceolate, 1–2-pinnate-pinnatifid, 4–20 × 1–4 cm, bearing scattered short, unbranched, glandular hairs on principal veins;

petioles shorter than blades.

subsessile, irregularly ovate to oblong and often irregularly cleft, 2.5–6.5 × 1–3 cm, bearing multicellular gland-tipped hairs and elongate rhizoidlike hairs on petiole;

margin fringed with minute, paired, roundish scales.

Blades

2 cell layers thick between veins.

Gametophytes

composed entirely of branching filaments.

unknown.

Venation

pinnate, without unconnected false veins.

flabellate with many unconnected false veins.

Soral

involucres terminal on lateral veins at base of lobes, conic, not flaring at mouth;

involucral lips not dark-edged.

involucres 5–15 per leaf, marginal on leaf apices, narrowly conic with flaring lips.

2n

= 72, 108, 144.

= 68.

Trichomanes boschianum

Trichomanes membranaceum

Habitat In deeply sheltered grottoes on noncalcareous rocks Terrestrial in acid humus
Elevation 150–800 m (500–2600 ft) below 10 m (below 0 ft)
Distribution
from FNA
AL; AR; GA; IL; IN; KY; NC; OH; SC; TN; VA; WV; Mexico in Chihuahua
[WildflowerSearch map]
from FNA
MS; Mexico; Central America; South America; epiphytic and on rock; West Indies
[BONAP county map]
Discussion

Although earlier treated as synonymous with the tropical American Trichomanes radicans Swartz, recent authors have agreed that Trichomanes boschianum is a distinct taxon endemic to eastern North America. It exists as fertile diploids and tetraploids with occasional sterile triploids. Diploid cytotypes are prevalent in western localities, and polyploids are more common to the east. Although occurring in climatically moderated habitats, most populations suffer heavy mortality from sporadic droughts. The plants are very slow to regrow, and many populations are currently but a fraction of their size of 20 years ago. They seldom show evidence of sexual reproduction although gametophyte colonies of this species may be found in the vicinity of fertile sporophytes. Identity of these gametophytes has been confirmed by enzyme electrophoresis, but most occurrences of independent Trichomanes gametophytes in the eastern United States have been shown by this method to be those of T. intricatum (D. R. Farrar 1985).

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

Trichomanes membranaceum resembles species of subg. Didymoglossum in its growth form and chromosome number, and it has been considered by some authors to be of that subgenus. Its marginal scales, absence of stellate hairs, and leaf blades 2 cell layers thick set it apart from other species of subg. Didymoglossum and all other American Trichomanes.

The single population reported from Harrison County, Mississippi, in 1929 (E. T. Wherry 1964) may be extirpated, and no other occurrences of Trichomanes membranaceum are currently known in the flora. Because it is a common and adaptable species of varied habitats throughout tropical America, occurrences along the Gulf Coast and in Florida are not unlikely.

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

Source FNA vol. 2. FNA vol. 2.
Parent taxa Hymenophyllaceae > Trichomanes Hymenophyllaceae > Trichomanes
Sibling taxa
T. holopterum, T. intricatum, T. krausii, T. lineolatum, T. membranaceum, T. petersii, T. punctatum
T. boschianum, T. holopterum, T. intricatum, T. krausii, T. lineolatum, T. petersii, T. punctatum
Synonyms Lecanium membranaceum
Name authority Sturm: Ned. Kruidk. Arch. 5(2): 160. (1861) Linnaeus: Sp. Pl. 2: 1097. (1753)
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