Selaginella Explained

Selaginella is the sole genus in the monotypic family (i.e. a family that contains only a single genus) Selaginellaceae, the spikemosses or lesser clubmosses, a type of vascular plant.

This family is distinguished from Lycopodiaceae (the clubmosses) by having scale-leaves bearing a ligule and by having spores of two types. They are sometimes included in an informal paraphyletic group called the "fern allies". The species S. moellendorffii is an important model organism. Its genome has been sequenced by the United States Department of Energy's Joint Genome Institute.[1] The name Selaginella was erected by Palisot de Beauvois solely for the species Selaginella selaginoides, which turns out (with the closely related Selaginella deflexa) to be a clade that is sister to all other Selaginellas, so any definitive subdivision of the species into separate genera leaves two taxa in Selaginella, with the hundreds of other species in new or resurrected genera.

Selaginella occurs mostly in the tropical regions of the world, with a handful of species to be found in the arctic-alpine zones of both hemispheres.[2] Fossils assignable to the modern genus are known spanning over 300 million years from the Late Carboniferous to the present.[3]

Description

Selaginella species are creeping or ascendant plants with simple, scale-like leaves (microphylls) on branching stems from which roots also arise. The stems are aerial, horizontally creeping on the substratum (as in Selaginella kraussiana), sub-erect (Selaginella trachyphylla) or erect (as in Selaginella erythropus). The vascular steles are polystelic protosteles. Stem section shows the presence of more than two protosteles. Each stele is made up of diarch (having two strands of xylem[4]) and exarch (growing outward in) xylems. The steles are connected with the cortex by means of many tube-like structures called trabeculae, which are modified endodermal cells with casparian strips on their lateral walls. The stems contain no pith.

In Selaginella, each microphyll and sporophyll has a small scale-like outgrowth called a ligule at the base of the upper surface.[5] The plants are heterosporous with spores of two different size classes, known as megaspores and microspores.[6]

Unusual for the lycopods, which nearly always have microphylls with a single unbranched vein, the microphylls of a few Selaginella species contain a branched vascular trace.[7]

Under dry conditions, some species of Selaginella can survive dehydration. In this state, they may roll up into brown balls and be uprooted, but can rehydrate under moist conditions, become green again and resume growth. This phenomenon is known as poikilohydry, and poikilohydric plants such as Selaginella bryopteris are sometimes referred to as resurrection plants.[8]

There is no evidence of whole genome duplication in Selaginella's evolutionary history. Instead they have gone through tandem gene duplications, which is particularly noticeable in genes relevant for desiccation tolerance.[9]

Taxonomy

Some scientists still place the Selaginellales in the class Lycopodiopsida (often misconstructed as "Lycopsida").[10] [11] Some modern authors recognize three generic divisions of Selaginella: Selaginella, Bryodesma Sojak 1992, and Lycopodioides Boehm 1760. Lycopodioides would include the North American species S. apoda and S. eclipes, while Bryodesma would include S. rupestris (as Bryodesma rupestre). Stachygynandrum is also sometimes used to include the bulk of species.

The first major attempt to define and subdivide the group was by Palisot de Beauvois[12] in 1803-1805. He established the genus Selaginella as a monotypic genus, and placed the bulk of species in Stachygynandrum. Gymnogynum was another monotypic genus, but that name is superseded by his own earlier name of Didiclis. This turns out, today, to be a group of around 45-50 species also known as the Articulatae, since his genus Didiclis/Gymnogynum was based on Selaginella plumosa. He also described the genus Diplostachyum to include a group of species similar to Selaginella apoda. Spring inflated the genus Selaginella to hold all selaginelloid species four decades later.

Phylogenetic studies by Korall & Kenrick[13] determined that the Euselaginella group, comprising solely the type species, Selaginella selaginoides and a closely related Hawaiian species, Selaginella deflexa, is a basal and anciently diverging sister to all other Selaginella species. Beyond this, their study split the remainder of species into two broad groups, one including the Bryodesma species, the Articulatae, section Ericetorum Jermy and others, and the other centered on the broad Stachygynandrum group.

Zhang & Zhou, 2015 classification

Species

See main article: List of Selaginella species. There are about 750 known species of Selaginella.[15] They show a wide range of characters; the genus is overdue for a revision which might include subdivision into several genera. Species of spikemoss include:

A few species of Selaginella are desert plants known as "resurrection plants", because they curl up in a tight, brown or reddish ball during dry times, and uncurl and turn green in the presence of moisture. Other species are tropical forest plants that appear at first glance to be ferns.

Cultivation

A number of Selaginella species are popular plants for cultivation, mostly tropical species. Some of the species popularly cultivated and actively available commercially include:

Notes and References

  1. Web site: Selaginella moellendorffii v1.0 . 2007 . . . 2009-04-08.
  2. Web site: Selaginella kraussiana | PlantZAfrica.
  3. Bek . Jiří . Libertín . Milan . Drábková . Jana . June 2009 . Selaginella labutae sp. nov., a new compression herbaceous lycopsid and its spores from the Kladno–Rakovník Basin, Bolsovian of the Czech Republic . Review of Palaeobotany and Palynology . en . 155 . 3–4 . 101–115 . 10.1016/j.revpalbo.2007.12.010. 2009RPaPa.155..101B .
  4. Web site: Diarch . The Free Dictionary.
  5. Book: Stace, C. A.. Stace, C. A.. 2010. New Flora of the British Isles. Third. Cambridge University Press. Cambridge, U.K.. 9780521707725.
  6. Petersen. Kurt B.. Burd. Martin. 2018. The adaptive value of heterospory: Evidence from Selaginella. Evolution. en. 72. 5. 1080–1091. 10.1111/evo.13484. 29645092. 4800398. 1558-5646. free.
  7. Wagner . Warren H. . Beitel . Joseph M. . Wagner . Florence S. . 1982-11-19 . Complex Venation Patterns in the Leaves of Selaginella : Megaphyll-Like Leaves in Lycophytes . Science . en . 218 . 4574 . 793–794 . 1982Sci...218..793W . 10.1126/science.218.4574.793 . 0036-8075 . 17771037 . 44904740.
  8. Book: The Standard Cyclopedia of Horticulture. Liberty Hyde Bailey. The Macmillan company . 1916 . 5 . 2920–2921; 3639 .
  9. VanBuren . Robert . Ching . Man Wai . Ou . Shujun . Pardo . Jeremy . Bryant . Doug . Jiang . Ning . Mockler . Todd C. . Edger . Patrick . Michael . Todd P. . Extreme haplotype variation in the desiccation- tolerant clubmoss Selaginella lepidophylla . Nature Communications . 2018 . 9 . 13 . 13 . 10.1038/s41467-017-02546-5. 29296019 . 5750206 . 2018NatCo...9...13V .
  10. Book: Clugston, M. . Dictionary of Science . Penguin Reference Library . 2014 . 978-0-141-98682-1 . 4th . London . 743 . en.
  11. Book: Walker, Peter . Chambers Science and Technology Dictionary . Chambers . 1992 . 0-550-13239-2 . 4th . Edinburgh NewYork . 999 . en.
  12. Palisot de Beauvois (1805): Prodrome des cinquième et sixième familles de l'Æthéogamie, les mousses, les lycopodes.
  13. Korall & Kenrick (2004): The phylogenetic history of Selaginellaceae based on DNA sequences from the plastid and nucleus: extreme substitution rates and rate heterogeneity. Molecular Phylogenetics and Evolution, Volume 31, Issue 3, June 2004, Pages 852-864
  14. Verdoorn, F., ed. (1938): Manual of Pteridology: J. Walton and A. H. G. Alston, Lycopodinae, pp. 500-506. Martinus Nijhoff, The Hague. 640pp, HB.
  15. Christenhusz, M. J. M. . Byng, J. W. . amp . 2016 . The number of known plants species in the world and its annual increase . Phytotaxa . 261 . 201–217 . 10.11646/phytotaxa.261.3.1 . 3 . free .

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