Vascular plant

Vascular plants (from Latin vasculum 'duct'), also called tracheophytes (/trəˈkiː.əˌfaɪts/)[5][6] or collectively Tracheophyta (from Ancient Greek τραχεῖα ἀρτηρία (trakheîa artēría) 'windpipe', and φυτά (phutá) 'plants'),[6] form a large group of land plants (c. 300,000 accepted known species)[7] that have lignified tissues (the xylem) for conducting water and minerals throughout the plant. They also have a specialized non-lignified tissue (the phloem) to conduct products of photosynthesis. Vascular plants include the clubmosses, horsetails, ferns, gymnosperms (including conifers), and angiosperms (flowering plants). Scientific names for the group include Tracheophyta,[8][4]: 251  Tracheobionta[9] and Equisetopsida sensu lato. Some early land plants (the rhyniophytes) had less developed vascular tissue; the term eutracheophyte has been used for all other vascular plants, including all living ones.

Vascular plants
Temporal range:
Common lady-fern, a non-seed-bearing plant
Lemon basil, a seed-bearing plant
Scientific classification
Kingdom: Plantae
Clade: Embryophytes
Clade: Polysporangiophytes
Clade: Tracheophytes
Sinnott, 1935[3] ex Cavalier-Smith, 1998[4]
Divisions
† Extinct

Historically, vascular plants were known as "higher plants," as it was believed that they were further evolved than other plants due to being more complex organisms. However, this is an antiquated remnant of the obsolete scala naturae, and the term is generally considered to be unscientific.[10]

Characteristics

Botanists define vascular plants by three primary characteristics:

  1. Vascular plants have vascular tissues which distribute resources through the plant. Two kinds of vascular tissue occur in plants: xylem and phloem. Phloem and xylem are closely associated with one another and are typically located immediately adjacent to each other in the plant. The combination of one xylem and one phloem strand adjacent to each other is known as a vascular bundle.[11] The evolution of vascular tissue in plants allowed them to evolve to larger sizes than non-vascular plants, which lack these specialized conducting tissues and are thereby restricted to relatively small sizes.
  2. In vascular plants, the principal generation or phase is the sporophyte, which produces spores and is diploid (having two sets of chromosomes per cell). (By contrast, the principal generation phase in non-vascular plants is the gametophyte, which produces gametes and is haploid - with one set of chromosomes per cell.)
  3. Vascular plants have true roots, leaves, and stems, even if some groups have secondarily lost one or more of these traits.

Cavalier-Smith (1998) treated the Tracheophyta as a phylum or botanical division encompassing two of these characteristics defined by the Latin phrase "facies diploida xylem et phloem instructa" (diploid phase with xylem and phloem).[4]: 251 

One possible mechanism for the presumed evolution from emphasis on haploid generation to emphasis on diploid generation is the greater efficiency in spore dispersal with more complex diploid structures. Elaboration of the spore stalk enabled the production of more spores and the development of the ability to release them higher and to broadcast them farther. Such developments may include more photosynthetic area for the spore-bearing structure, the ability to grow independent roots, woody structure for support, and more branching.

Phylogeny

A proposed phylogeny of the vascular plants after Kenrick and Crane 1997[12] is as follows, with modification to the gymnosperms from Christenhusz et al. (2011a),[13] Pteridophyta from Smith et al.[14] and lycophytes and ferns by Christenhusz et al. (2011b) [15] The cladogram distinguishes the rhyniophytes from the "true" tracheophytes, the eutracheophytes.[12]

Polysporangiates
 
Tracheophytes
Eutracheophytes
Euphyllophytina
Lignophytes
Spermatophytes
 

†Pteridospermatophyta (seed ferns)

 
 

Cycadophyta (cycads)

 
 

Pinophyta (conifers)

 
 

Ginkgophyta (ginkgo)

 
 

Gnetophyta

 
 

Magnoliophyta (flowering plants)

 
 
 

†Progymnospermophyta

 
 
Pteridophyta
 
 

Pteridopsida (true ferns)

 
 

Marattiopsida

 
 

Equisetopsida (horsetails)

 
 

Psilotopsida (whisk ferns & adders'-tongues)

 
 

†Cladoxylopsida

 
 
 
 
Lycophytina
 

Lycopodiophyta

 
 

†Zosterophyllophyta

 
 
 
 

†Rhyniophyta

 
 
 
 

†Aglaophyton

 
 

†Horneophytopsida

 
 

This phylogeny is supported by several molecular studies.[14][16][17] Other researchers state that taking fossils into account leads to different conclusions, for example that the ferns (Pteridophyta) are not monophyletic.[18]

Hao and Xue presented an alternative phylogeny in 2013 for pre-euphyllophyte plants.[19]

Polysporangiophytes
 

†Horneophytaceae

 
Tracheophytes
 

†Cooksoniaceae

 
 
 

†Aglaophyton

 
 
 

†Rhyniopsida

 
 
 

†Catenalis

 
 
 

†Aberlemnia

 
 
 

†Hsuaceae

 
 
 

†Renaliaceae

 
Eutracheophytes
 
 

†Adoketophyton

 
 

†?Barinophytopsida

 
 

†Zosterophyllopsida

 
 
 
Microphylls
 

†Hicklingia

 
 
 

†Gumuia

 
 
 

†Nothia

 
 
 

†Zosterophyllum deciduum

 
 

Lycopodiopsida

 
 
 
 
 
 
 

†Yunia

 
Euphyllophytes
 

†Eophyllophyton

 
 
 

†Trimerophytopsida

 
Megaphylls
Moniliformopses
 

†Ibyka

 
 
 

†Pauthecophyton

 
 
 

†Cladoxylopsida

 
 

Polypodiopsida

 
 
 
 
Radiatopses
 

†Celatheca

 
 
 

†Pertica

 
Lignophytes
 

†Progymnosperms
(paraphyletic)

 
 

Spermatophytes

 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
Rhyniopsids
Renalioids

Nutrient distribution
Photographs showing xylem elements in the shoot of a fig tree (Ficus alba): crushed in hydrochloric acid, between slides and cover slips

Water and nutrients in the form of inorganic solutes are drawn up from the soil by the roots and transported throughout the plant by the xylem. Organic compounds such as sucrose produced by photosynthesis in leaves are distributed by the phloem sieve-tube elements.

The xylem consists of vessels in flowering plants and of tracheids in other vascular plants. Xylem cells are dead hard-walled hollow cells arranged to form files of tubes that function in the transport of water. A tracheid cell-wall usually contains the polymer lignin.

The phloem, on the other hand, consists of living cells called sieve-tube members. Between the sieve-tube members are sieve plates, which have pores to allow molecules to pass through. Sieve-tube members lack such organs as nuclei or ribosomes, but cells next to them, the companion cells, function to keep the sieve-tube members alive.

Transpiration

The most abundant compound in all plants, as in all cellular organisms, is water, which has an important structural role and a vital role in plant metabolism. Transpiration is the main process of water movement within plant tissues. Plants constantly transpire water through their stomata to the atmosphere and replace that water with soil moisture taken up by their roots. The movement of water out of the leaf stomata sets up a transpiration pull or tension in the water-column in the xylem vessels or tracheids. The pull is the result of water surface tension within the cell walls of the mesophyll cells, from the surfaces of which evaporation takes place when the stomata are open. Hydrogen bonds exist between water molecules, causing them to line up; as the molecules at the top of the plant evaporate, each pulls the next one up to replace it, which in turn pulls on the next one in line. The draw of water upwards may be entirely passive and can be assisted by the movement of water into the roots via osmosis. Consequently, transpiration requires the plant to expend very little energy on water movement. Transpiration assists the plant in absorbing nutrients from the soil as soluble salts.

Absorption

Living root cells passively absorb water in the absence of transpiration pull via osmosis creating root pressure. It is possible for there to be no evapotranspiration and therefore no pull of water towards the shoots and leaves. This is usually due to high temperatures, high humidity, darkness or drought.

Conduction

Xylem and phloem tissues each play a part in the conduction processes within plants. Sugars are conducted throughout the plant in the phloem; water and other nutrients through the xylem. Conduction occurs from a source to a sink for each separate nutrient. Sugars are produced in the leaves (a source) by photosynthesis and transported to the growing shoots and roots (sinks) for use in growth, cellular respiration or storage. Minerals are absorbed in the roots (a source) and transported to the shoots to allow cell division and growth.[20]

See also

References
  1. D. Edwards; Feehan, J. (1980). "Records of Cooksonia-type sporangia from late Wenlock strata in Ireland". Nature. 287 (5777): 41–42. Bibcode:1980Natur.287...41E. doi:10.1038/287041a0. S2CID 7958927.
  2. Laura Wegener Parfrey; Daniel J G Lahr; Andrew H Knoll; Laura A Katz (16 August 2011). "Estimating the timing of early eukaryotic diversification with multigene molecular clocks" (PDF). Proceedings of the National Academy of Sciences of the United States of America. 108 (33): 13624–9. Bibcode:2011PNAS..10813624P. doi:10.1073/PNAS.1110633108. ISSN 0027-8424. PMC 3158185. PMID 21810989. Wikidata Q24614721.
  3. Sinnott, E. W. 1935. Botany. Principles and Problems, 3d edition. McGraw-Hill, New York.
  4. Cavalier-Smith, T. (1998), "A revised six-kingdom system of life" (PDF), Biological Reviews of the Cambridge Philosophical Society, 73 (3): 203–266, doi:10.1111/j.1469-185X.1998.tb00030.x, PMID 9809012, S2CID 6557779, archived from the original (PDF) on 2018-03-29
  5. "vascular plant | Definition, Characteristics, Taxonomy, Examples, & Facts | Britannica". www.britannica.com. Retrieved 2022-03-22.
  6. "Tracheophyta - an overview | ScienceDirect Topics". www.sciencedirect.com. Retrieved 2022-03-22.
  7. Christenhusz, M. J. M. & Byng, J. W. (2016). "The number of known plants species in the world and its annual increase". Phytotaxa. 261 (3): 201–17. doi:10.11646/phytotaxa.261.3.1.
  8. Abercrombie, Michael; Hickman, C. J.; Johnson, M. L. (1966). A Dictionary of Biology. Penguin Books.
  9. "ITIS Standard Report Page: Tracheobionta". Retrieved September 20, 2013.
  10. "Vascular Plants: Definition, Classification, Characteristics & Examples". Sciencing. Retrieved 2022-03-22.
  11. "Xylem and Phloem". Basic Biology. 26 August 2020.
  12. Kenrick, Paul; Crane, Peter R. (1997). The Origin and Early Diversification of Land Plants: A Cladistic Study. Washington, D.C.: Smithsonian Institution Press. ISBN 1-56098-730-8.
  13. Christenhusz, Maarten J. M.; Reveal, James L.; Farjon, Aljos; Gardner, Martin F.; Mill, R.R.; Chase, Mark W. (2011). "A new classification and linear sequence of extant gymnosperms" (PDF). Phytotaxa. 19: 55–70. doi:10.11646/phytotaxa.19.1.3.
  14. Smith, Alan R.; Pryer, Kathleen M.; Schuettpelz, E.; Korall, P.; Schneider, H.; Wolf, Paul G. (2006). "A classification for extant ferns" (PDF). Taxon. 55 (3): 705–731. doi:10.2307/25065646. JSTOR 25065646.
  15. Christenhusz, Maarten J. M.; Zhang, Xian-Chun; Schneider, Harald (2011). "A linear sequence of extant families and genera of lycophytes and ferns" (PDF). Phytotaxa. 19: 7–54. doi:10.11646/phytotaxa.19.1.2.
  16. Pryer, K. M.; Schneider, H.; Smith, AR; Cranfill, R; Wolf, PG; Hunt, JS; Sipes, SD (2001). "Horsetails and ferns are a monophyletic group and the closest living relatives to seed plants". Nature. 409 (6820): 618–22. Bibcode:2001Natur.409..618S. doi:10.1038/35054555. PMID 11214320. S2CID 4367248.
  17. Pryer, K. M.; Schuettpelz, E.; Wolf, P. G.; Schneider, H.; Smith, A. R.; Cranfill, R. (2004). "Phylogeny and evolution of ferns (monilophytes) with a focus on the early leptosporangiate divergences". American Journal of Botany. 91 (10): 1582–1598. doi:10.3732/ajb.91.10.1582. PMID 21652310.
  18. Rothwell, G.W. & Nixon, K.C. (2006). "How Does the Inclusion of Fossil Data Change Our Conclusions about the Phylogenetic History of Euphyllophytes?". International Journal of Plant Sciences. 167 (3): 737–749. doi:10.1086/503298. S2CID 86172890.
  19. Hao, Shougang & Xue, Jinzhuang (2013), The early Devonian Posongchong flora of Yunnan: a contribution to an understanding of the evolution and early diversification of vascular plants, Beijing: Science Press, p. 366, ISBN 978-7-03-036616-0, retrieved 2019-10-25
  20. Taiz, Lincoln; Zeiger, Eduardo (2002). "5, 6, 10". Plant Physiology (3 ed.). Sunderland, Massachusetts: Sinauer Associates.

Bibliography
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