Biology:Argyrochosma formosa

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Short description: Species of fern in the family Pteridaceae

Argyrochosma formosa
a bluish-green triangular leaf divided into small segments connected by black axes
Argyrochosma formosa, showing black axes and triangular shape of leaf
Scientific classification edit
Kingdom: Plantae
Clade: Tracheophytes
Division: Polypodiophyta
Class: Polypodiopsida
Order: Polypodiales
Family: Pteridaceae
Genus: Argyrochosma
Species:
A. formosa
Binomial name
Argyrochosma formosa
(Liebm.) Windham
Synonyms
  • Allosorus formosus Liebm.
  • M.Martens & Galeotti, nom. illeg. hom. (Liebm.) Mickel & Beitel
  • (Liebm.) Maxon, nom. superfl. Pellaea puchella
  • Cincinalis pulchella Fée
  • Cassebeera pulchella J.Sm.
  • T.Moore Hemionitis formosa
  • Allosorus pulchellus Farwell
  • (Liebm.) Christenh. Notholaena formosa
  • Cheilanthes formosa (Liebm.) R.M.Tryon
  • Platyloma pulchellum Pellaea formosa

Argyrochosma formosa is a fern known from eastern and central Mexico and Guatemala. It grows on rocky slopes, particularly on limestone. Unlike many members of the genus, it lacks white powder on the underside of its leaves. First described as a species in 1842, it was transferred to the new genus Argyrochosma (the "false cloak ferns") in 1987, recognizing their distinctness from the "cloak ferns" (Notholaena sensu stricto).

Description

Argyrochosma formosa is a medium-sized epipetric fern. The rhizome is compact and horizontal.[1] It bears linear scales 3 to 6 millimeters (0.1 to 0.2 in)[2] or 6 to 9 millimeters (0.2 to 0.4 in) long and 0.3 millimeters (0.01 in) wide,[1] hair-tipped[2] and with entire (toothless) margins.[3] They range from tan to dark orange[1] or rusty in color[2] and feel oily-viscid.[3]

The fronds arise in clumps from the rhizome. They are from about 15 to 40 centimeters (5.9 to 16 in) long,[3][1] sometimes as short as 10 centimeters (3.9 in), and 2 to 7 centimeters (0.8 to 3 in) broad.[2] Of their length, about 25% to 50% is made up by the stipe (the stalk of the leaf, below the blade), which is shiny or sometimes glaucous and round, hairless, and reddish-brown to dark purple or black in color.[1][3] The rhizome scales may continue to the base of the stipe.[2][3]

The leaf blades are tripinnate to quadripinnate (cut into pinnae, pinnules and pinnulets, those sometimes fully cut) and range in shape from ovate to long-deltate (triangular) to ovate-lanceolate.[1][3] The rachis (leaf axis) is round, rather than flattened.[1] The rachis and the axes of the leaf segments are all dark in color; the color stops abruptly at a joint at the base of the leaf segment.[1] Each blade bears 6 to 9 pairs of pinnae, borne alternately or nearly oppositely on the rachis,[1] with an acute (pointed) tip.[3] The ultimate segments of the blade are orbicular (circular) or inequilaterally cordate (asymmetrically heart-shaped), 3 to 4 millimeters (0.1 to 0.2 in) long,[1] sometimes to 6 millimeters (0.2 in).[2] They are borne on short stalks.[3] The underside of the leaf lacks the farina (powder) that characterizes many members of the genus,[1] although both upper and lower surfaces of the leaf are usually glaucous.[3]

The sori lie along the veins, forming a band 0.5 to 1 millimeter (0.02 to 0.04 in) wide[1] on the outermost quarter of the vein.[3] The leaf edges are curved under,[3] sometimes to the point of touching one another,[2] but otherwise not modified into false indusia. Fertile segments often fold along their long axis, giving them a sagittate (arrowhead-like) shape. Specimens from Oaxaca were found to be apomictic triploids, with a chromosome number of n = 2n = 81.[1]

While it is similar in overall appearance to A. incana, it is easily distinguished from that species by its lack of farina. In Mexico, the only other member of the genus to lack farina is A. microphylla, which has smaller leaf segments, chestnut-brown, rather than black, leaf axes,[1] a grooved rachis and dry rhizome scales.[3]

Taxonomy

The species was first described in 1842 as Allosorus pulchellus by Martin Martens & Henri Guillaume Galeotti, based on material collected by Galeotti in Mexico.[4] The epithet pulchellus means "small and beautiful"[5] and presumably reflects the aesthetic appeal of the species, which they described as "charmante".[4] However, that name had already been used in 1836 for a different species, the former Cheilanthes pulchella, by Carl Borivoj Presl, rendering it nomenclaturally illegitimate. Frederik Liebmann recognized the issue and corrected it by giving Martens & Galeotti's species the replacement name Allosorus formosus in 1849;[6] the epithet formosus means "beautiful".[7]

Delineating natural genera in the cheilanthoids has proven to be extremely difficult, and other placements of the species were subsequently put forward, mostly as replacement names for A. pulchellus in other genera using the same epithet. Fée transferred it to Pellaea as Pellaea pulchella in 1852.[8] In 1857, Thomas Moore, in his Index Filicum, transferred it to Platyloma, a genus he recognized as a segregate from Pellaea, as Platyloma pulchellum.[9] John Smith, in 1866, preferred to recognize a different cheilanthoid segregate, Cincinalis, and placed it there as Cincinalis pulchella.[10] In 1922, William Ralph Maxon created a new combination for Liebmann's name in Pellaea, as Pellaea formosa due to the illegitimacy of Martens & Galeotti's name,[11] although subsequent changes to the practice of nomenclature would make it superfluous. Oliver Atkins Farwell, following a program of reviving what he considered to be senior synonyms, gave Cassebeera priority over Pellaea and transferred the species there as Cassebeera pulchella in 1931.[12]

Maxon and Charles Alfred Weatherby placed Pellaea formosa within a group of ferns closely related to Notholaena nivea, but declined to make a nomenclatural transfer until the classification of the cheilanthoids was better understood.[13] Both Edwin Copeland and Weatherby suggested in the 1940s that this group of ferns might represent a distinct genus of its own.[14] This was finally addressed in 1987 by Michael D. Windham, who was carrying out phylogenetic studies of these genera. He elevated Notholaena sect. Argyrochosma to become the genus Argyrochosma,[15] and transferred this species to that genus as A. formosa.[16] Meanwhile, John Mickel and Joe Beitel had transferred the species to Cheilanthes as C. formosa in their monograph on the ferns of Oaxaca, which was published in 1988;[17] Mickel and Alan R. Smith recognized Argyrochosma in 2004 when preparing a fern flora of Mexico.[1] In 2018, Maarten J. M. Christenhusz transferred the species to Hemionitis as H. formosa, as part of a program to consolidate the cheilanthoid ferns into that genus.[18]

underside of fern frond divided into cordate segments connected by black axes, the black color passing into the base, spores visible but no white powder
Argyrochosma formosa, showing lack of farina and dark color of axes passing into leaf segments

Phylogenetic studies have shown that A. formosa is a sister species to A. microphylla; these two species form a clade sister to another clade containing A. jonesii and A. lumholtzii.[19] All four species lack farina, and their common ancestor is hypothesized to have diverged from the ancestor of the rest of the genus before farina production developed in the latter.[20]

Distribution and habitat

Argyrochosma formosa is distributed from the northernmost provinces of Mexico through eastern and central Mexico to Chiapas and into Guatemala.[1]

In Mexico, it grows on dry rocky slopes and in ravines, often on limestone, as well as in thorny scrub. It has been found growing in mortar at Monte Albán.[1] Most common in similar habitats in Guatemala, it also occurs on hillsides and riverbanks, and in forests and thickets.[2] It is found at an altitude from 1,250 to 2,700 meters (4,100 to 8,860 ft).[1]

Notes and references

References

  1. ↑ 1.00 1.01 1.02 1.03 1.04 1.05 1.06 1.07 1.08 1.09 1.10 1.11 1.12 1.13 1.14 1.15 1.16 1.17 Mickel & Smith 2004, p. 66.
  2. ↑ 2.0 2.1 2.2 2.3 2.4 2.5 2.6 2.7 Stolze 1981, p. 337.
  3. ↑ 3.00 3.01 3.02 3.03 3.04 3.05 3.06 3.07 3.08 3.09 3.10 3.11 Tryon & Weatherby 1956, p. 100.
  4. ↑ 4.0 4.1 Martens & Galeotti 1842, p. 47.
  5. ↑ Short & George 2013, p. 236.
  6. ↑ Liebmann 1849, p. 220.
  7. ↑ Short & George 2013, p. 175.
  8. ↑ Fée 1852.
  9. ↑ Moore 1857, p. lxvi.
  10. ↑ Smith 1866, p. 178.
  11. ↑ Maxon 1922, p. 61.
  12. ↑ Farwell 1931, p. 281.
  13. ↑ Maxon & Weatherby 1939, p. 4.
  14. ↑ Windham 1987, p. 37.
  15. ↑ Windham 1987, p. 38.
  16. ↑ Windham 1987, p. 40.
  17. ↑ Mickel & Beitel 1988, p. 115.
  18. ↑ Christenhusz, Fay & Byng 2018, p. 14.
  19. ↑ Sigel et al. 2011, p. 558.
  20. ↑ Sigel et al. 2011, p. 559.

Works cited

Wikidata ☰ Q15597716 entry



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