Equisetidae: Difference between revisions
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'''Equisetopsida''', or '''Sphenopsida''' is |
'''Equisetopsida''', or '''Sphenopsida''', is an ancient [[Class (biology)|class]] of [[plant]]s. Living species are commonly known as '''horsetails''' and typically grow in wet areas, with needle-like leaves radiating at regular intervals from a single vertical stem. Equisetopsida is placed in the botanical [[Division (biology)|division]] of [[fern]]s (Pteridophyta),<ref name="Smith 2006">{{cite journal | last=Smith | first=Alan R.| coauthors= Kathleen M. Pryer, Eric Schuettpelz, Petra Korall, Harald Schneider, & Paul G. Wolf | year=2006 | title= A classification for extant ferns | url=http://www.pryerlab.net/publication/fichier749.pdf | journal=Taxon | volume= 55 | issue=3 | pages= 705–731 }}</ref> though sometimes regarded as a separate division '''Equisetophyta''' (also as '''Sphenophyta''' or '''Arthrophyta'''). |
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==Morphology== |
==Morphology== |
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Revision as of 07:27, 3 June 2008
| Equisetidae | |
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| Equisetum telmateia | |
| Scientific classification | |
| Kingdom: | |
| Division: | |
| Class: | Equisetopsida C. Agardh
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| Orders | |
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Sphenopsida | |
 | This article needs additional citations for verification. (February 2008) |
Equisetopsida, or Sphenopsida, is an ancient class of plants. Living species are commonly known as horsetails and typically grow in wet areas, with needle-like leaves radiating at regular intervals from a single vertical stem. Equisetopsida is placed in the botanical division of ferns (Pteridophyta),[2] though sometimes regarded as a separate division Equisetophyta (also as Sphenophyta or Arthrophyta).
Morphology
The Sphenophytes comprise photosynthesising, "segmented", hollow stems, sometimes filled with pith. At the junction ("node", see diagram) between each segment is a whorl of leaves. In the only extant genus Equisetum, these are small leaves (microphylls) with a singular vascular trace. However, sphenophyte leaves probably arose by the reduction of a megaphyll, as evidenced by early fossil forms such as Sphenophyllum, in which the leaves are broad with branching veins.[3] The plumbing of these leaves is interesting: the vascular traces trifurcate at the junctions, with one thread going to the microphyll, and the other two moving left and right to merge with the new branches of their neighbours. The vascular system itself curiously resembles that of the vascular plants' eustele, which evolved convergently. A primary xylem contains carinal canals; in the Calamitales, secondary xylem (but not secondary phloem) can be secreted as the cambium grows outwards, producing a woody stem, and allowing the plants to grow as high as 10m. The cortex itself contains valecular canals; due to the softer nature of the phloem, these are very rarely seen in fossil instances.
The plant does not bear a coherent root system but underground rhizomes, from which roots and aerial axes emerge.
The plant contains an intercalary meristem: that is to say, each segment of the stem grows as the plant gets taller. This contrasts with the seed plants, which contain an apical meristem - i.e. new growth comes only from growing tips (and widening of stems). Growth was determinate - i.e. the plants' phenotype dictated a maximum height, which the plant would grow to then get no higher.
Sphenophytes bear cones (technically strobili, sing. strobilus) at the tips of some stems. These cones comprise spirally arranged sporophores, which bear spores in four clusters, and in extant sphenophytes cover the spores externally - like four sacs hanging from an umbrella, with its handle embedded in the central cone body. In extinct groups, further protection was afforded to the spores by the presence of whorls of bracts - big pointy microphylls protruding from the cone.
The spores themselves bear characteristic elaters, distinctive spring-like attachments which are hygroscopic: i.e. they change their configuration in the presence of water, helping the spores move and aiding their dispersal. Dispersal is aided in the first instance by laterally dehiscing sporangia, which pop open and scatter spores.
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The extant horsetails are mostly homosporous, but this is conspicuously not the case in the past.
Fossil record
The extant horsetails represent a tiny fraction of Sphenophyte diversity in the past. There were three orders. First were the Pseudoborniales, which first appeared in the Devonian.[1] Second, the Sphenophyllales which were a dominant member of the Carboniferous understory, and prospered until the mid and early Permian respectively. The Equisetales existed alongside the Sphenophyllales, but diversified as that group disappeared into extinction, gradually dwindling in diversity to today's single genus Equisetum.
Systematics
The horsetails and their fossil relatives have long been recognized as quite distinct from other seedless vascular plants.[4] In fact, the group is so unlike other living and fossil plants that its relationship to other plants has long been considered problematic.[5]
Because of the unclear relationships of the group, the rank botanists assign to it varies from order to division. When recognized as a separate division, the literature uses many possible names, including Arthrophyta[5], Sphenophyta[1][6], or Equisetophyta. Other authors have regarded the same group as a class, either within a division consisting of the vascular plants or, more recently, within an expanded fern group. When ranked as a class, the group has been termed the Equisetopsida[7] or Sphenopsida.[8]
References
- ^ a b c Taylor, Thomas N. (1993). The Biology and Evolution of Fossil Plants. Englewood Cliffs, NJ: Prentice Hall. pp. 303–305. ISBN 0-13-651589-4.
{{cite book}}: Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ Smith, Alan R. (2006). "A classification for extant ferns" (PDF). Taxon. 55 (3): 705–731.
{{cite journal}}: Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ Rutishauser, R. (1999). "Polymerous Leaf Whorls in Vascular Plants: Developmental Morphology and Fuzziness of Organ Identities". International Journal of Plant Sciences. 160 (6): 81–103. doi:10.1086/314221. Retrieved 2008-01-31.
- ^ Eames, Arthur J. (1936). Morphology of Vascular Plants (Lower Groups). New York and London: McGraw-Hill Book Company. pp. 110–115.
- ^ a b Bold (1987). Morphology of Plants and Fungi (5th edition ed.). New York: Harper-Collins. pp. 371–387, 478, 506–514. ISBN 0-06-040838-1.
{{cite book}}:|edition=has extra text (help); Check|isbn=value: checksum (help); Unknown parameter|coauthors=ignored (|author=suggested) (help); Unknown parameter|fisrt=ignored (help) - ^ Gifford, Ernest M. (1988). Morphology and Evolution of Vascular Plants (3rd ed.). New York: W. H. Freeman and Company. pp. 175–207. ISBN 0-7167-1946-0.
{{cite book}}: Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ Kenrick, Paul (1997). The Origin and Early Diversification of Land Plants: A Cladistic Study. Washington, D. C.: Smithsonian Institution Press. pp. 241–242. ISBN 1-56098-730-8.
{{cite book}}: Unknown parameter|coauthors=ignored (|author=suggested) (help) - ^ Stewart, Wilson N. (1993). Paleobotany and the Evolution of Plants (2nd edition ed.). Cambridge: Cambridge University Press. ISBN 0-521-38294-7.
{{cite book}}:|edition=has extra text (help); Unknown parameter|coauthors=ignored (|author=suggested) (help)
