Huperzia
J. Bot. (Schrader) 1800(2): 126. 1801 Gemma fir-moss [for Johann Pete. 1816.
Plants terrestrial or on rock, erect to decumbent. Roots produced in apical portions of shoot, migrating downward in cortex to emerge at soil level. Horizontal stems absent. Shoots determinate (entire plant dying after several years of spore production) or indeterminate (entire plant not dying after several years), clustered to decumbent, round in cross-section, equally dichotomously branched, 2–16 mm diam. including leaves. Leaves not in distinct ranks [ranked], not imbricate [imbricate], appressed, ascending to spreading, triangular, lanceolate to oblanceolate, monomorphic or varying in size according to seasonal growth patterns; juvenile (basal or proximal) leaves mostly larger than mature (terminal or distal) leaves, margins irregularly dentate to entire, ± irregularly roughened by papillae formed by marginal cells. Gemmiferous branchlets and attached gemmae formed among leaves in same phyllotactic spiral, gemmae articulate and abscising at maturity, deltoid, 2.5–6 X 3–6 mm, with 4 leaves flattened into 1 plane, 2 large lateral leaves, and 1 abaxial, 1 adaxial leaf. Sporangia reniform, borne individually at adaxial base of unmodified or reduced leaf, fertile leaves in zones or scattered along shoot. Spores pitted to shallowly grooved, sides at equator concave, angles truncate. Gametophytes nonphotosynthetic, mycorrhizal, subterranean, unbranched, linear to elliptic in outline, paraphyses numerous, uniseriate; ring meristem absent. x = 67, 68.
Distribution
Temperate, alpine, and arctic regions, and tropical Asian mountains.
Discussion
We distinguish the temperate and arctic Huperzia as a distinct genus because of its many differences from the tropical epiphytes, in particular the remarkably complex and specialized shoots, gemmiferous branchlets and gemmae, and the unbranched gametophytes.
In the area of central to northwestern Canada, numerous scattered collections of plants of this genus were formerly identified as Huperzia selago. Although many of them may be that species, a strong possibility exists that other, rather similar species may be represented. A careful study of materials from Saskatchewan, northern Alberta, northern Manitoba, and Mackenzie and Keewatin districts of the Northwest Territories, and perhaps a wider area, is needed. Collectors are urged to take samples from as many localities as possible. The general area is shown in the map for H. selago (cf. W. J. Cody and D. M. Britton 1989).
Hybrids between species of North American Huperzia are extremely common. They are recognizable as hybrids because, in this genus (as opposed to Diphasiastrum and Lycopodiella), they usually have abortive spores that vary greatly in size and shape. The abortion of spores can be recognized readily under a high-powered dissecting microscope or a low-powered compound microscope. In all cases, the hybrids are intermediate in characters: if one parent has numerous teeth on the leaf margins and the other has entire margins, the hybrid will have few, inconspicuous teeth; if one parent has oblanceolate leaves, the other subulate leaves, the hybrid will have narrowly lanceolate leaves. In our descriptions we have not included the shape and dimensions of the gemmae of the different species, but they do differ in size, overall outlines, and gemmae leaf shapes; the hybrids are intermediate in these characters.
In the flora, Huperzia includes at least one sexual allopolyploid and six sterile hybrid taxa that reproduce by gemmae. Because of the subtle differences among the basic species and their propensity to form vegetatively reproducing hybrids, most Huperzia species and hybrids (except H. lucidula) have been confused with H. selago, populations of which are confined to northeastern North America. Many of the sterile hybrids often occur at considerable distances from the parents, suggesting that wind may disperse the gemmae. The aerodynamics involved would be an interesting subject for study. Spores of two species coming together at the same site by long-distance dispersal may also explain some disjunctions.
Species 10–15 (7 in the flora).
Selected References
Lower Taxa
Key
| 1 | Leaves narrowly obovate, teeth 1–8, irregular; stomates abaxial; spores (23–)24–26(–29) µm. | Huperzia lucidula |
| 1 | Leaves lanceolate or oblanceolate, entire or with 1– 3 low teeth; stomates on both surfaces; spores 25– 41 µm. | > 2 |
| 2 | Largest leaves oblanceolate; shoots 12–20 cm; mainly terrestrial in shaded forests along streams. | Huperzia occidentalis |
| 2 | Largest leaves lanceolate or widest at base, or sides nearly parallel; shoots mainly 8–15 cm (except H. miyoshiana to 25 cm); mainly of rocky cliffs and talus habitats, or acidic bogs, ditches, meadows, and marshes. | > 3 |
| 3 | Largest leaves lanceolate with sides nearly parallel much of length; stomates 1–25 per 1/2 leaf on adaxial surface. | Huperzia porophila |
| 3 | Largest leaves lanceolate to ovate or nearly triangular and widest at base or sides nearly parallel much of length; stomates more than 30 per 1/2 leaf on adaxial surface. | > 4 |
| 4 | Shoots with weak annual constrictions; gemmiferous branchlets and gemmae formed in 1 pseudowhorl at end of annual growth. | Huperzia selago |
| 4 | Shoots without annual constrictions; gemmiferous branchlets and gemmae produced in 1–3 pseudowhorls at end of annual growth or throughout mature shoots. | > 5 |
| 5 | Mature distal leaves mostly 2–3.5 mm, somewhat triangular. | Huperzia appalachiana |
| 5 | Mature distal leaves mostly 3.5–5.5 mm, lanceolate or ovate. | > 6 |
| 6 | Mature shoots 12–18(–25) cm; gemmae in 2–3 pseudowhorls at end of annual growth; gemma lateral leaves 1.2–1.8 mm wide; mostly mossy boulders and marshes in conifer forests. | Huperzia miyoshiana |
| 6 | Mature shoots 8–11 cm; gemmiferous branchlets and gemmae produced throughout mature portion of shoot; gemma lateral leaves 1.5–2 mm wide; alpine and subalpine mossy meadows. | Huperzia haleakalae |