Open main menu

The Division Lycopodiophyta (sometimes called lycophyta or lycopods) is a tracheophyte subgroup of the Kingdom Plantae. It is one of the oldest lineages of extant (living) vascular plants and contains extinct plants like Baragwanathia that have been dated from the Silurian (ca. 425 million years ago).[3][4] Members of Lycopodiophyta were some of the dominating plant species of the Carboniferous period.[5] These species reproduce by shedding spores and have macroscopic alternation of generations, although some are homosporous while others are heterosporous. Most members of Lycopodiophyta bear a protostele, and the sporophyte generation is dominant.[6] They differ from all other vascular plants in having microphylls, leaves that have only a single vascular trace (vein) rather than the much more complex megaphylls found in ferns and seed plants.

Lycopodiophyta
Temporal range: 428–0 Ma
Silurian[1] to recent
Lycopodiella inundata 001.jpg
Lycopodiella inundata
Scientific classification e
Kingdom: Plantae
Clade: Tracheophytes
Division: Lycopodiophyta
D.H.Scott 1900[2]
Classes

Lycopodiopsida - clubmosses
Isoetopsida - spikemosses, quillworts, scale trees
† Zosterophyllopsida - zosterophylls

Contents

ClassificationEdit

There are around 1,290[7] (Christenhusz & Byng 2016[8]) living (extant) species of Lycopodiophyta which are generally divided into three extant orders (Lycopodiales, Isoetales, and Selaginellales), in addition to extinct groups. There is some variation in how the extant orders are grouped into classes: they may be put into a single class, Lycopodiopsida sensu lato;[9][10] they may be put into two classes, Lycopodiopsida sensu stricto for Lycopodiales and Isoetopsida for Isoetales and Selaginellales;[11] or they may be put into three classes, one order in each.[citation needed] The system which uses two classes for extant species is:

The extant orders each have a single family with a total of 12 genera and 1290 known species (Christenhusz & Byng 2016[8]).

The following phylogram shows a likely relationship between Lycopodiophyta orders.


Lycopodiophyta
Lycopodiopsida

Lycopodiales

Drepanophycales †

Isoetopsida

Selaginellales

Lepidodendrales †

Pleuromeiales †

Isoetales

The following is another phylogram showing the evolution of Lycopodiophytes. Note the Cooksonia-like plants and zosterophylls are a paraphyletic grade of stem group Lycopodiophytes.[1][12][13]


Tracheophyta

"Cooksonia" hemisphaerica Lang 1937

Rhyniopsida

Eutracheophytes

Cooksonia Lang 1937 emend. Gonez & Gerrienne 2010 non Druce 1905 (Cooksonioids s.s.)

†basal group 1

†basal group 2 (Renalioids)

Lycopodiophytina

Hicklingia

†basal zosterophylls

†core zosterophylls

Nothia

"Zosterophyllum" deciduum Gerrienne 1988

Lycopodiopsida

Asteroxylales

Drepanophycales

Lycopodiales

Protolepidodendrales

Selaginellales

Lepidodendrales

Pleuromeiales

Isoetales

Euphyllophytes

Notes:

EvolutionEdit

The members of this division have a long evolutionary history, and fossils are abundant worldwide, especially in coal deposits. In fact, most known genera are extinct. The Silurian species Baragwanathia longifolia represents the earliest identifiable Lycopodiophyta, while some Cooksonia seem to be related. Lycopodolica is another Silurian genus which appears to be an early member of this group.[14]

Fossils ascribed to the Lycopodiophyta first appear in the Silurian period, along with a number of other vascular plants. Phylogenetic analysis places them at the base of the vascular plants; they are distinguished by their microphylls and by transverse dehiscence of their sporangia (as contrasted with longitudinal in other vascular plants). Sporangia of living species are borne on the upper surfaces of microphylls (called sporophylls). In some groups, these sporophylls are clustered into strobili.

Devonian fossil trees from Svalbard, growing in equatorial regions, raise the possibility that they drew down enough carbon dioxide significantly to change the earth's climate.[15]

During the Carboniferous Period, tree-like Lycopodiophyta (such as Lepidodendron) formed huge forests that dominated the landscape. The complex ecology of these tropical rainforests collapsed during the mid Pennsylvanian due to a change in climate.[16]

Unlike modern trees, leaves grew out of the entire surface of the trunk and branches, but would fall off as the plant grew, leaving only a small cluster of leaves at the top. Their remains formed many fossil coal deposits. In Fossil Park, Glasgow, Scotland, fossilized Lycopodiophyta trees can be found in sandstone. The trees are marked with diamond-shaped scars where they once had leaves.

The group also evolved roots independently from the rest of the vascular plants.[17]

The Lycopodiophyta had their maximum diversity in the Upper Carboniferous, particularly tree-like Lepidodendron and Sigillaria, that dominated tropical wetlands. In Euramerica these became apparently extinct in the Late Pennsylvanian, as a result of a transition to a much drier climate, to give way to conifers, ferns and horsetails. In Cathaysia (now South China) tree-like Lycopodiophytes survived into the Permian. Nevertheless, lycopsids are rare in the Lopingian (latest Permian), but regained dominance in the Induan (earliest Triassic), particularly Pleuromeia. After the worldwide Permian–Triassic extinction event Lycopodiophyta pioneered the repopulation of habitats as opportunistic plants. The heterogeneity of the terrestrial plant communities increased markedly during the Middle Triassic when plant groups like sphenopsids, ferns, pteridosperms, cycadophytes, ginkgophytes and conifers resurfaced and diversified quickly.[18]

CharacteristicsEdit

Club-mosses are homosporous, but the genera Selaginella and Isoetes are heterosporous, with female spores larger than the male, and gametophytes forming entirely within the spore walls. A few species of Selaginella such as S. apoda and S. rupestris are also viviparous; the gametophyte develops on the mother plant, and only when the sporophyte's primary shoot and root is developed enough for independence is the new plant dropped to the ground.[19] Club-moss gametophytes are mycoheterotrophic and long-lived, residing underground for several years before emerging from the ground and progressing to the sporophyte stage.[20]

The spores of Lycopodiophyta are highly flammable and so have been used in fireworks.[21] Huperzine A, a chemical isolated from the Chinese firmoss Huperzia serrata, is under investigation as a possible treatment for Alzheimer's disease.[22]

Microbial AssociationsEdit

Lycophytes form associations with microbes such as fungi and bacteria, including arbuscular mycorrhizal and endophytic associations.

Arbuscular mycorrhizal associations have been characterized in all stages of the lycophyte lifecycle: mycoheterotrophic gametophyte, photosynthetic surface-dwelling gametophyte, young sporophyte, and mature sporophyte.[23] Arbuscular mycorrhizae have been found in Selaginella spp. roots and vesicles.[24]

During the mycoheterotrophic gametophyte lifecycle stage, lycophytes gain all of their carbon from subterranean glomalean fungi. In other plant taxa, glomalean networks transfer carbon from neighboring plants to mycoheterotrophic gametophytes. Something similar could be occurring in Huperzia hypogeae gametophytes which associate with the same glomalean phenotypes as nearby Huperzia hypogeae sporophytes.[20]

Fungal endophytes have been found in many species of lycophyte, however the function of these endophytes in host plant biology is not known. Endophytes of other plant taxa perform roles such as improving plant competitive fitness, conferring biotic and abiotic stress tolerance, promoting plant growth through phytohormone production or production of limiting nutrients.[25] However, some endophytic fungi in lycophytes do produce medically relevant compounds. Shiraia sp Slf14 is an endophytic fungus present in Huperzia serrata that produces Huperzine A, a biomedical compound which has been approved as a drug in China and a dietary supplement in the U.S. to treat Alzheimer’s Disease.[26] This fungal endophyte can be cultivated much more easily and on a much larger scale than H. serrata itself which could increase the availability of Huperzine A as a medicine.

GalleryEdit

ReferencesEdit

  1. ^ a b Kenrick, Paul; Crane, Peter R. (1997). The Origin and Early Diversification of Land Plants: A Cladistic Study. Washington, D. C.: Smithsonian Institution Press. pp. 339–340. ISBN 978-1-56098-730-7.
  2. ^ James L. Reveal, Indices Nominum Supragenericorum Plantarum Vascularium
  3. ^ Rickards, R.B. (2000). "The age of the earliest club mosses: the Silurian Baragwanathia flora in Victoria, Australia". Geological Magazine. 137 (2): 207–209. doi:10.1017/s0016756800003800.
  4. ^ McElwain, Jenny C.; Willis, K. G.; Willis, Kathy; McElwain, J. C. (2002). The evolution of plants. Oxford [Oxfordshire]: Oxford University Press. ISBN 978-0-19-850065-0.
  5. ^ Ranker, T. A.; Hauler, C. H. (2008). Biology and evolution of ferns and lycophytes. Cambridge: Cambridge University Press.
  6. ^ Eichhorn, Evert, and Raven (2005). Biology of Plants, Seventh Edition. 381-388.
  7. ^ Callow, R. S.; Cook, Laurence Martin (1999). Genetic and evolutionary diversity: the sport of nature. Cheltenham: S. Thornes. p. 8. ISBN 978-0-7487-4336-0.
  8. ^ a b Christenhusz, M. J. M. & Byng, J. W. (2016). "The number of known plants species in the world and its annual increase". Phytotaxa. Magnolia Press. 261 (3): 201–217. doi:10.11646/phytotaxa.261.3.1.
  9. ^ "www.ncbi.nlm.nih.gov". Retrieved 2009-03-19.
  10. ^ Pteridophyte Phylogeny Group (2016). "A community-derived classification for extant lycophytes and ferns". Journal of Systematics and Evolution. 54 (6): 563–603. doi:10.1111/jse.12229.
  11. ^ Yatsentyuk, S.P.; Valiejo-Roman, K.M.; Samigullin, T.H.; Wilkström, N.; Troitsky, A.V. (2001). "Evolution of Lycopodiaceae Inferred from Spacer Sequencing of Chloroplast rRNA Genes". Russian Journal of Genetics. 37 (9): 1068–73. doi:10.1023/A:1011969716528.
  12. ^ Crane, P.R.; Herendeen, P.; Friis, E.M. (2004), "Fossils and plant phylogeny", American Journal of Botany, 91 (10): 1683–99, doi:10.3732/ajb.91.10.1683, PMID 21652317, retrieved 2011-01-27
  13. ^ Gonez, P. & Gerrienne, P. (2010a), "A New Definition and a Lectotypification of the Genus Cooksonia Lang 1937", International Journal of Plant Sciences, 171 (2): 199–215, doi:10.1086/648988
  14. ^ Raymond, A.; Gensel, P. & Stein, W.E. (2006). "Phytogeography of Late Silurian macrofloras". Review of Palaeobotany and Palynology. 142 (3–4): 165–192. doi:10.1016/j.revpalbo.2006.02.005.
  15. ^ https://www.cardiff.ac.uk/news/view/163982-tropical-fossil-forests-unearthed-in-arctic-norway
  16. ^ Sahney, S., Benton, M.J. & Falcon-Lang, H.J. (2010). "Rainforest collapse triggered Pennsylvanian tetrapod diversification in Euramerica" (PDF). Geology. 38 (12): 1079–1082. doi:10.1130/G31182.1.CS1 maint: multiple names: authors list (link)
  17. ^ Stepwise and independent origins of roots among land plants | Nature
  18. ^ Moisan, Philippe; Voigt, Sebastian (2013). "Lycopsids from the Madygen Lagerstätte (Middle to Late Triassic, Kyrgyzstan, Central Asia)". Review of Palaeobotany and Palynology. 192: 42–64. doi:10.1016/j.revpalbo.2012.12.003. Retrieved 2015-03-20.
  19. ^ Cryptogams: Algae, Bryophyta and Pterldophyta
  20. ^ a b Winther, J. L.; Friedman, W. E. (2008). "Arbuscular mycorrhizal associations in Lycopodicaceae". New Phytologist. 177: 790–801.
  21. ^ Cobb, B (1956) A Field Guide to Ferns and their related families: Northeastern and Central North America with a section on species also found in the British Isles and Western Europe (Peterson Field Guides), 215
  22. ^ Zangara, A (2003). "The psychopharmacology of huperzine A: an alkaloid with cognitive enhancing and neuroprotective properties of interest in the treatment of Alzheimer's disease". Pharmacology Biochemistry and Behavior. 75 (3): 675–686. doi:10.1016/S0091-3057(03)00111-4. PMID 12895686.
  23. ^ Winther, J. L.; Friedman, W. E. (2008). "Arbuscular mycorrhizal associations in Lycopodicaceae". New Phytologist. 177: 790–801.
  24. ^ Lara-Pérez, L. A.; Valdés-Baizabal, M. D. (2015). "Mycorrhizal associations of ferns and lycopods of central Veracruz, Mexico". Symbiosis. 65: 85–92.
  25. ^ Bacon, C.W.; Hinton, D. M. (2007). "Bacterial endophytes: the endophytic niche, its occupants, and its utility". In Gnanamanickam, S. S. (ed.). Plant-Associated Bacteria (1 ed.). Dorcrecht: Springer. pp. 155–194.
  26. ^ Zhu, D. (2010). "A novel endophytic Huperzine A-producing fungus, Shirai sp. Slf14, isolated from Huperzia serrata". Journal of Applied Microbiology. 109: 1469–1478.

External linksEdit