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Salvinia

Salvinia
Salvinia minima
Scientific classification Edit this classification
Kingdom: Plantae
Clade: Tracheophytes
Division: Polypodiophyta
Class: Polypodiopsida
Order: Salviniales
Family: Salviniaceae
Genus: Salvinia
Ség.
Type species
Salvinia natans
(L.) All.
Species

See text

Salvinia or watermosses[1] is a genus of free-floating aquatic ferns in the family Salviniaceae. The genus is named in honor of 17th-century Italian naturalist Anton Maria Salvini, and the generic name was first published in 1754 by French botanist Jean-François Séguier in Plantae Veronenses, a description of the plants found around Verona.[2] Twelve species are recognized, at least three of which (S. molesta, S. herzogii, and S. minima) are believed to be hybrids in part because their sporangia are found to be empty.

Salvinia is related to the other water ferns, including the mosquito fern Azolla. Recent sources include both Azolla and Salvinia in Salviniaceae, although each genus was formerly given its own family.

Salvinia, like the other ferns in order Salviniales, are heterosporous, producing spores of differing sizes. However, leaf development in Salvinia is unique. The upper side of the floating leaf, which appears to face the stem axis, is morphologically abaxial.[3]

Salvinia cucullata is one of just two fern species for which a reference genome has been published.[4]

Description

Small, floating aquatics with creeping stems, branched, bearing hairs on the leaf surface papillae but no true roots. Leaves are in trimerous whorls, with two leaves green, sessile or short-petioled, flat, entire and floating, and one leaf finely dissected, petiolate, rootlike and pendent. Submerged leaves bearing sori that are surrounded by basifixed membranous indusia (sporocarps).

They bear sporocarps of two types, either megasporangia that are few in number (approximately 10), each with single megaspore, or many microsporangia, each with 64 microspores. Spores are of two kinds and sizes, both globose, trilete. Megagametophytes and microgametophytes protruding through sporangium wall; megagametophytes floating on water surface with archegonia directed downward; microgametophytes remaining fixed to sporangium wall.

The small, hairlike growths, known as trichomes or microgametical follicles, are not known to have any productive function, and are currently a biological mystery.

Phylogeny

Phylogeny of Salvinia[5][6]

S. natans (L.) All. (Floating watermoss)

S. cucullata Roxburgh ex Bory

S. minima Baker (Water spangles)

S. auriculata Aublet 1775 (Eared watermoss; African payal; butterfly fern)

S. ×molesta Mitch. (Kariba weed)

S. oblongifolia von Martius

Other species include:

Evolutionary history

The geography of Salvinia fossil material suggests members of the genus may have been broadly distributed during the Tertiary.[7][8]

Distribution

Distribution is mostly tropical, in North America, Mexico, West Indies, Central America, South America, Eurasia and Africa, including Madagascar, South Borneo, Asia.

Economic impacts

Giant salvinia (Salvinia molesta) is a commonly introduced invasive weed in warm climates, but is native to South America. It grows rapidly, up to two times its dry weight in 2+12 days, and forms dense mats over still waters. A tiny weevil, Cyrtobagous salviniae, has been used successfully to biologically control giant salvinia.[9]

One proposed use takes advantage of the hydrophobic trichomes, which do not repel oil. This makes them candidates for mopping up oil spills, as they become saturated with oil in thirty seconds. S. molesta trichomes served as a model for a similarly hydrophobic synthetic polycarbonate.[10]

Salvinia effect

The salvinia effect describes the stabilization of an air layer upon a submerged hydrophobic (water repellent) surface by hydrophilic (water loving) pins. This physic-chemical phenomenon was discovered on the floating fern Salvinia molesta by the botanist Wilhelm Barthlott (Universität Bonn) while working on the Lotus effect and was described in cooperation with the physicist Thomas Schimmel (Karlsruher Institut für Technologie), fluid mechanist Alfred Leder (Universität Rostock) and their colleagues in 2010.

References

  1. ^ NRCS. "Salvinia". PLANTS Database. United States Department of Agriculture (USDA). Retrieved 28 October 2015.
  2. ^ Pl. Veron. 3: 52. 1754.
  3. ^ J. G. Croxdale 1978, 1979, 1981.
  4. ^ Li, Fay-Wei; Brouwer, Paul; Carretero-Paulet, Lorenzo; Cheng, Shifeng; de Vries, Jan; Delaux, Pierre-Marc; Eily, Ariana; Koppers, Nils; Kuo, Li-Yaung (2018-07-02). "Fern genomes elucidate land plant evolution and cyanobacterial symbioses". Nature Plants. 4 (7): 460–472. doi:10.1038/s41477-018-0188-8. ISSN 2055-0278. PMC 6786969. PMID 29967517.
  5. ^ Nitta, Joel H.; Schuettpelz, Eric; Ramírez-Barahona, Santiago; Iwasaki, Wataru; et al. (2022). "An Open and Continuously Updated Fern Tree of Life". Frontiers in Plant Science. 13: 909768. doi:10.3389/fpls.2022.909768. PMC 9449725. PMID 36092417.
  6. ^ "Tree viewer: interactive visualization of FTOL". FTOL v1.6.0 [GenBank release 259]. 2024. Retrieved 8 March 2024.
  7. ^ Wang, Li; Qing-Qing Xu; Jian-Hua Jin (2014). "A reconstruction of the fossil Salvinia from the Eocene of Hainan Island, South China". Review of Palaeobotany and Palynology. 203: 12–21. Bibcode:2014RPaPa.203...12W. doi:10.1016/j.revpalbo.2013.12.005.
  8. ^ McNair, D.M.; D.Z. Stults; B. Axsmith; M.H. Alford; J.E. Starnes (2019). "Preliminary investigation of a diverse megafossil floral assemblage from the middle Miocene of southern Mississippi, USA" (PDF). Palaeontologia Electronica. 22 (2). doi:10.26879/906.
  9. ^ Ward, Colin (2013-09-05). "Salvinia biocontrol". CSIROpedia. Retrieved 2022-08-28.
  10. ^ Coxworth, Ben (August 24, 2016). "Oil spill clean-up material functions like a fern". newatlas.com. Retrieved 2016-08-25.

Sources