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Marchantiophyta

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Not to be confused with the genus of flowering plants, Hepatica, that may also be called "liverwort".
Liverworts
Temporal range: 472–0 Ma
Mid-Ordovician[1] to recent
Haeckel Hepaticae.jpg
"Hepaticae" from Ernst Haeckel's Kunstformen der Natur, 1904
Scientific classification e
Kingdom: Plantae
Division: Marchantiophyta
Stotler & Stotl.-Crand., 1977[2] emend. 2000[3]
Classes and Orders

Haplomitriopsida Stotler & Stotl.-Crand.

Jungermanniopsida Stotler & Stotl.-Crand.

Marchantiopsida Stotler & Stotl.-Crand.

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The Marchantiophyta Listeni/mɑːrˌkæntiˈɒfᵻtə/ are a division of non-vascular bryophyte land plants commonly referred to as hepatics or liverworts. Like other bryophytes, they have a gametophyte-dominant life cycle, in which cells of the plant carry only a single set of genetic information.

It is estimated that there are about 9000 species of liverworts. Some of the more familiar species grow as a flattened leafless thallus, but most species are leafy with a form very much like a flattened moss. Leafy species can be distinguished from the apparently similar mosses on the basis of a number of features, including their single-celled rhizoids. Leafy liverworts also differ from most (but not all) mosses in that their leaves never have a costa (present in many mosses) and may bear marginal cilia (very rare in mosses). Other differences are not universal for all mosses and liverworts, but the occurrence of leaves arranged in three ranks, the presence of deep lobes or segmented leaves, or a lack of clearly differentiated stem and leaves all point to the plant being a liverwort.

Liverworts are typically small, usually from 2–20 mm wide with individual plants less than 10 cm long, and are therefore often overlooked. However, certain species may cover large patches of ground, rocks, trees or any other reasonably firm substrate on which they occur. They are distributed globally in almost every available habitat, most often in humid locations although there are desert and arctic species as well. Some species can be a nuisance in shady green-houses or a weed in gardens.[4]

Physical characteristics

Description

Most liverworts are small, usually from Lua error in Module:Convert at line 1851: attempt to index local 'en_value' (a nil value). wide with individual plants less than Lua error in Module:Convert at line 1851: attempt to index local 'en_value' (a nil value). long,[5] so they are often overlooked. The most familiar liverworts consist of a prostrate, flattened, ribbon-like or branching structure called a thallus (plant body); these liverworts are termed thallose liverworts. However, most liverworts produce flattened stems with overlapping scales or leaves in two or more ranks, the middle rank is often conspicuously different from the outer ranks; these are called leafy liverworts or scale liverworts.[6][7] (See the gallery below for examples.)

A thallose liverwort, Lunularia cruciata

Liverworts can most reliably be distinguished from the apparently similar mosses by their single-celled rhizoids.[8] Other differences are not universal for all mosses and all liverworts;[7] but the lack of clearly differentiated stem and leaves in thallose species, or in leafy species the presence of deeply lobed or segmented leaves and the presence of leaves arranged in three ranks, all point to the plant being a liverwort.[9][10] Unlike any other embryophytes, most liverworts contain unique membrane-bound oil bodies containing isoprenoids in at least some of their cells, lipid droplets in the cytoplasm of all other plants being unenclosed.[11] The overall physical similarity of some mosses and leafy liverworts means that confirmation of the identification of some groups can be performed with certainty only with the aid of microscopy or an experienced bryologist.

Liverworts have a gametophyte-dominant life cycle, with the sporophyte dependent on the gametophyte.[11] Cells in a typical liverwort plant each contain only a single set of genetic information, so the plant's cells are haploid for the majority of its life cycle. This contrasts sharply with the pattern exhibited by nearly all animals and by most other plants. In the more familiar seed plants, the haploid generation is represented only by the tiny pollen and the ovule, while the diploid generation is the familiar tree or other plant.[12] Another unusual feature of the liverwort life cycle is that sporophytes (i.e. the diploid body) are very short-lived, withering away not long after releasing spores.[13] Even in other bryophytes, the sporophyte is persistent and disperses spores over an extended period.[citation needed]

Life cycle

Life cycle of a Marchantia-like liverwort

The life of a liverwort starts from the germination of a haploid spore to produce a protonema, which is either a mass of thread-like filaments or else a flattened thallus.[14][15] The protonema is a transitory stage in the life of a liverwort, from which will grow the mature gametophore ("gamete-bearer") plant that produces the sex organs. The male organs are known as antheridia (singular: antheridium) and produce the sperm cells. Clusters of antheridia are enclosed by a protective layer of cells called the perigonium (plural: perigonia). As in other land plants, the female organs are known as archegonia (singular: archegonium) and are protected by the thin surrounding perichaetum (plural: perichaeta).[7] Each archegonium has a slender hollow tube, the "neck", down which the sperm swim to reach the egg cell.

Liverwort species may be either dioicous or monoicous. In dioicous liverworts, female and male sex organs are borne on different and separate gametophyte plants. In monoicous liverworts, the two kinds of reproductive structures are borne on different branches of the same plant.[16] In either case, the sperm must move from the antheridia where they are produced to the archegonium where the eggs are held. The sperm of liverworts is biflagellate, i.e. they have two tail-like flagellae that enable them to swim short distances,[17] provided that at least a thin film of water is present. Their journey may be assisted by the splashing of raindrops. In 2008, Japanese researchers discovered that some liverworts are able to fire sperm-containing water up to 15 cm in the air, enabling them to fertilize female plants growing more than a metre from the nearest male.[18]

When sperm reach the archegonia, fertilisation occurs, leading to the production of a diploid sporophyte. After fertilisation, the immature sporophyte within the archegonium develops three distinct regions: (1) a foot, which both anchors the sporophyte in place and receives nutrients from its "mother" plant, (2) a spherical or ellipsoidal capsule, inside which the spores will be produced for dispersing to new locations, and (3) a seta (stalk) which lies between the other two regions and connects them.[17] When the sporophyte has developed all three regions, the seta elongates, pushing its way out of the archegonium and rupturing it. While the foot remains anchored within the parent plant, the capsule is forced out by the seta and is extended away from the plant and into the air. Within the capsule, cells divide to produce both elater cells and spore-producing cells. The elaters are spring-like, and will push open the wall of the capsule to scatter themselves when the capsule bursts. The spore-producing cells will undergo meiosis to form haploid spores to disperse, upon which point the life cycle can start again.

Asexual reproduction

Some liverworts are capable of asexual reproduction; in bryophytes in general "it would almost be true to say that vegetative reproduction is the rule and not the exception."[19] For example, in Riccia, when the older parts of the forked thalli die, the younger tips become separate individuals.[19]

Some thallose liverworts such as Marchantia polymorpha and Lunularia cruciata produce small disc-shaped gemmae in shallow cups.[20] Marchantia gemmae can be dispersed up to 120 cm by rain splashing into the cups.[21] In Metzgeria, gemmae grow at thallus margins.[22] Marchantia polymorpha is a common weed in greenhouses, often covering the entire surface of containers;[23]:230 gemma dispersal is the "primary mechanism by which liverwort spreads throughout a nursery or greenhouse."[23]:231

Ecology

Today, liverworts can be found in many ecosystems across the planet except the sea and excessively dry environments, or those exposed to high levels of direct solar radiation.[24] As with most groups of living plants, they are most common (both in numbers and species) in moist tropical areas.[25] Liverworts are more commonly found in moderate to deep shade, though desert species may tolerate direct sunlight and periods of total desiccation.

Classification

Relationship to other plants

Traditionally, the liverworts were grouped together with other bryophytes (mosses and hornworts) in the Division Bryophyta, within which the liverworts made up the class Hepaticae (also called Marchantiopsida).[7][26] However, since this grouping makes the Bryophyta paraphyletic, the liverworts are now usually given their own division.[27] The use of the division name Bryophyta sensu lato is still found in the literature, but more frequently the Bryophyta now is used in a restricted sense to include only the mosses.

Two hypotheses on the phylogeny of land plants (embryophyta).[citation needed]

Another reason that liverworts are now classified separately is that they appear to have diverged from all other embryophyte plants near the beginning of their evolution. The strongest line of supporting evidence is that liverworts are the only living group of land plants that do not have stomata on the sporophyte generation.[28] Among the earliest fossils believed to be liverworts are compression fossils of Pallaviciniites from the Upper Devonian of New York.[29] These fossils resemble modern species in the Metzgeriales.[30] Another Devonian fossil called Protosalvinia also looks like a liverwort, but its relationship to other plants is still uncertain, so it may not belong to the Marchantiophyta. In 2007, the oldest fossils assignable to the liverworts were announced, Metzgeriothallus sharonae from the Givetian (Middle Devonian) of New York, United States.[31] However, in 2010, five different types of fossilized liverwort spores were found in Argentina, dating to the much earlier Middle Ordovician, around 470 million years ago.[1][32]

Internal classification

Bryologists classify liverworts in the division Marchantiophyta. This divisional name is based on the name of the most universally recognized liverwort genus Marchantia.[33] In addition to this taxon-based name, the liverworts are often called Hepaticophyta. This name is derived from their common Latin name as Latin was the language in which botanists published their descriptions of species. This name has led to some confusion,[citation needed] partly because it appears to be a taxon-based name derived from the genus Hepatica which is actually a flowering plant of the buttercup family Ranunculaceae. In addition, the name Hepaticophyta is frequently misspelled in textbooks as Hepatophyta, which only adds to the confusion.

Although there is no consensus among bryologists as to the classification of liverworts above family rank,[34] the Marchantiophyta may be subdivided into three classes:[35][36][37][38]

The diagram at right summarizes a portion of a 2006 cladistic analysis of liverworts based upon three chloroplast genes, one nuclear gene, and one mitochondrial gene.[35]
Marchantiophyta

Haplomitriopsida

Haplomitriales


Treubiales




Marchantiopsida

Blasiales



Sphaerocarpales


Marchantiales



Jungermanniopsida

Metzgeriales (part)



Jungermanniales


Metzgeriales (part)





An updated classification by Söderström et al. 2016[41]

It is estimated that there are about 9000 species of liverworts, at least 85% of which belong to the leafy group.[3][42] Despite that fact, no liverwort genomes have been sequenced to date and only few genes identified and characterized.[43]

Economic importance

In ancient times, it was believed that liverworts cured diseases of the liver, hence the name.[44] In Old English, the word liverwort literally means liver plant.[45] This probably stemmed from the superficial appearance of some thalloid liverworts (which resemble a liver in outline), and led to the common name of the group as hepatics, from the Latin word hēpaticus for "belonging to the liver". An unrelated flowering plant, Hepatica, is sometimes also referred to as liverwort because it was once also used in treating diseases of the liver. This archaic relationship of plant form to function was based in the "Doctrine of Signatures".[46]

Liverworts have little direct economic importance today. Their greatest impact is indirect, through the reduction of erosion along streambanks, their collection and retention of water in tropical forests, and the formation of soil crusts in deserts and polar regions. However, a few species are used by humans directly. A few species, such as Riccia fluitans, are aquatic thallose liverworts sold for use in aquariums. Their thin, slender branches float on the water's surface and provide habitat for both small invertebrates and the fish that feed on them.

Gallery

A small collection of images showing liverwort structure and diversity:

See also

References

  1. ↑ 1.0 1.1 Walker, Matt. "Fossils of earliest land plants discovered in Argentina" [1]. (BBC, Earth News, 2010).
  2. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  3. ↑ 3.0 3.1 Lua error in package.lua at line 80: module 'strict' not found.
  4. ↑ Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, volume VI, page 19. (Chicago: Field Museum of Natural History, 1992). ISBN 0-914868-21-7.
  5. ↑ Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, volume I, pages 243-244. (New York: Columbia University Press, 1966)
  6. ↑ Kashyap, Shiv Ram. Liverworts of the Western Himalayas and the Panjab Plain, volume I, page 1. (New Delhi: The Chronica Botanica, 1929)
  7. ↑ 7.0 7.1 7.2 7.3 Schofield, W. B. Introduction to Bryology, pages 135-140. (New York: Macmillan, 1985). ISBN 0-02-949660-8.
  8. ↑ Nehira, Kunito. "Spore Germination, Protonemata Development and Sporeling Development", page 347 in Rudolf M. Schuster (Ed.), New Manual of Bryology, volume I. (Nichinan, Miyazaki, Japan: The Hattori Botanical Laboratory, 1983). ISBN 49381633045.
  9. ↑ Allison, K. W. & John Child. The Liverworts of New Zealand, pages 13-14. (Dunedin: University of Otago Press, 1975).
  10. ↑ Conard, Henry S. and Paul L. Redfearn, Jr. How to Know the Mosses and Liverworts, revised ed., pages 12-23. (Dubuque, Iowa: William C. Brown Co., 1979) ISBN 0-697-04768-7
  11. ↑ 11.0 11.1 Harold C. Bold, C. J. Alexopoulos, and T. Delevoryas. Morphology of Plants and Fungi, 5th ed., page 189. (New York: Harper-Collins, 1987). ISBN 0-06-040839-1.
  12. ↑ Fosket, Donald E. Plant Growth and Development: A Molecular Approach, page 27. (San Diego: Academic Press, 1994). ISBN 0-12-262430-0.
  13. ↑ Hicks, Marie L. Guide to the Liverworts of North Carolina, page 10. (Durham: Duke University Press, 1992). ISBN 0-8223-1175-5.
  14. ↑ Nehira, Kunito. "Spore Germination, Protonemata Development and Sporeling Development", pages 358-374 in Rudolf M. Schuster (Ed.), New Manual of Bryology, volume I. (Nichinan, Miyazaki, Japan: The Hattori Botanical Laboratory, 1983). ISBN 49381633045.
  15. ↑ Chopra, R. N. & P. K. Kumra. Biology of Bryophytes, pages 1-38. (New York: John Wiley & Sons, 1988). ISBN 0-470-21359-0.
  16. ↑ Malcolm, Bill & Nancy Malcolm. Mosses and Other Bryophytes: An Illustrated Glossary, pages 6 & 128. (New Zealand: Micro-Optics Press, 2000). ISBN 0-473-06730-7.
  17. ↑ 17.0 17.1 Campbell, Douglas H. The Structure and Development of Mosses and Ferns, pages 73-74. (London: The Macmillan Co., 1918)
  18. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  19. ↑ 19.0 19.1 Lua error in package.lua at line 80: module 'strict' not found.
  20. ↑ Smith, AJE (1989) The Liverworts of Britain and Ireland, Cambridge University Press, Cambridge.
  21. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  22. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  23. ↑ 23.0 23.1 Lua error in package.lua at line 80: module 'strict' not found.
  24. ↑ Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, volume I, pages 243-249. (New York: Columbia University Press, 1966).
  25. ↑ Pócs, Tamás. "Tropical Forest Bryophytes", page 59 in A. J. E. Smith (Ed.) Bryophyte Ecology. (London: Chapman and Hall, 1982). ISBN 0-412-22340-6.
  26. ↑ Crandall-Stotler, Barbara. & Stotler, Raymond E. "Morphology and classification of the Marchantiophyta". page 36-38 in A. Jonathan Shaw & Bernard Goffinet (Eds.), Bryophyte Biology. (Cambridge: Cambridge University Press:2000). ISBN 0-521-66097-1
  27. ↑ Goffinet, Bernard. "Origin and phylogenetic relationships of bryophytes". pages 124-149 in A. Jonathan Shaw & Bernard Goffinet (Eds.), Bryophyte Biology. (Cambridge: Cambridge University Press:2000). ISBN 0-521-66097-1
  28. ↑ Kenrick, Paul & Peter R. Crane. The Origin and Early Diversification of Land Plants: A Cladistic Study, page 59. (Washington, D. C.: Smithsonian Institution Press, 1997). ISBN 1-56098-730-8.
  29. ↑ Taylor, Thomas N. & Edith L. Taylor. The Biology and Evolution of Fossil Plants, page 139. (Englewood Cliffs, NJ: Prentice Hall, 1993). ISBN 0-13-651589-4.
  30. ↑ Oostendorp, Cora. The Bryophytes of the Palaeozoic and the Mesozoic, pages 70-71. (Bryophytum Bibliotheca, Band 34, 1987). ISBN 3-443-62006-X.
  31. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  32. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  33. ↑ Crandall-Stotler, Barbara. & Stotler, Raymond E. "Morphology and classification of the Marchantiophyta". page 63 in A. Jonathan Shaw & Bernard Goffinet (Eds.), Bryophyte Biology. (Cambridge: Cambridge University Press:2000). ISBN 0-521-66097-1
  34. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  35. ↑ 35.0 35.1 35.2 Lua error in package.lua at line 80: module 'strict' not found.
  36. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  37. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  38. ↑ 38.0 38.1 Lua error in package.lua at line 80: module 'strict' not found.
  39. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  40. ↑ Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, volume VI, page 26. (Chicago: Field Museum of Natural History, 1992). ISBN 0-914868-21-7.
  41. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  42. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  43. ↑ Lua error in package.lua at line 80: module 'strict' not found.
  44. ↑ Dittmer, Howard J. Phylogeny and Form in the Plant Kingdom, page 286. (Toronto: D. Van Nostrand Co., 1964)
  45. ↑ Raven, P. H., R. F. Evert, & S. E. Eichhorn. Biology of Plants, 7th ed., page 351. (New York: W. H. Freeman, 2005). ISBN 0-7167-1007-2.
  46. ↑ Stern, Kingsley R. Introductory Plant Biology, 5th ed., page 338. (Dubuque, Iowa: Wm. C. Brown Publishers, 1991) ISBN 0-697-09947-4.

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