Haplomitriopsida

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Haplomitriopsida
Temporal range: Early Permian–Recent
Untersuchungen uber Haplomitrium Hookeri (1843) plate XIII.jpg
Haplomitrium hookeri
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Division: Marchantiophyta
Class: Haplomitriopsida
Stotler & Stotl.-Crand., 1977
Type genus
Haplomitrium
Nees, 1833
Subgroups

See text.

Synonyms
  • Treubiopsida M.Stech, J.-P.Frahm, Hilger & W.Frey

Haplomitriopsida is a class of liverworts comprising fifteen species in three genera. Recent cladistic analyses of nuclear, mitochondrial, and plastid gene sequences place this monophyletic group as the basal sister group to all other liverworts. [1] [2] [3] [4] The group thus provides a unique insight into the early evolution of liverworts in particular and of land plants in general.

Contents

Description

Plants of Treubia grow as a prostrate leafy thallus. The bifid leaves extend like wings on either side of the midrib, or may be folded upwards and pressed close together, giving the plants a ruffled appearance. By contrast, Haplomitrium grows as a subterranean rhizome with erect leafy stems. The thin, rounded leaves are arranged around the upright stems, giving the appearance of a soft moss. The species Haplomitrium ovalifolium of Australia often has bifid leaves that are asymmetrical, somewhat like those in Treubia. [5]

Haplomitrium has a number of unique characters that distinguish it from other liverworts, such as lacking rhizoids. The vegetative stems possess a central water-conducting strand with large perforations derived from plasmodesmata. [6] This central strand is surrounded by a cylinder of cells that conduct food throughout the plant. Such an arrangement is evocative of the xylem and phloem found in vascular plants. Although some thalloid liverwort species in the Pallaviciniaceae also possess a central conducting strand, [7] Haplomitrium differs in having a food-conducting layer and in producing no callose.

Treubia also has features that differ from those found in other bryophytes, [8] such as the differentiation of five identifiable zones in the stem midrib. Unlike other leafy species, the oil bodies in its cells are restricted to certain clusters of cells, as they are in the Marchantiopsida. These oil body clusters appear as dark spots in the leaves when the plant is held up to the light. [9]

Diversity

Living representatives of the group exhibit an essentially Gondwanan distribution with its center of diversity in Australasia. Such a distribution implies that the modern genera radiated prior to the beginning of the Cretaceous when Gondwana broke apart. Schuster proposes that species distributed in the northern hemisphere "rafted" on the Indian subcontinent to Asia, then spread across the Bering Strait into North America. [10]

Most species in the Haplomitriopsida are found in south of the equator, though there are northern ones. The genus Treubia is restricted to the southern hemisphere, while Apotreubia has one species in New Guinea and another disjunct between eastern Asia and British Columbia. The genus Haplomitrium exhibits a wider distribution, with species in both North and South America, northern and central Europe, the Himalayas, Japan, and Australasia.

Classification

The orders, families, and genera within class Haplomitriopsida are as follows: [11]

Related Research Articles

<span class="mw-page-title-main">Marchantiophyta</span> Botanical division of non-vascular land plants

The Marchantiophyta are a division of non-vascular land plants commonly referred to as hepatics or liverworts. Like mosses and hornworts, they have a gametophyte-dominant life cycle, in which cells of the plant carry only a single set of genetic information. The division name was derived from the genus name Marchantia, named by French botanist Jean Marchant after his father.

<span class="mw-page-title-main">Marchantiales</span> Order of non-vascular plants known as liverworts

Marchantiales is an order of thallose liverworts that includes species like Marchantia polymorpha, a widespread plant often found beside rivers, and Lunularia cruciata, a common and often troublesome weed in moist, temperate gardens and greenhouses.

<span class="mw-page-title-main">Marchantiopsida</span> Class of liverworts

Marchantiopsida is a class of liverworts within the phylum Marchantiophyta. The species in this class are known as complex thalloid liverworts. The species in this class are widely distributed and can be found worldwide. Complex oil bodies are only found in the gametophyte.

<span class="mw-page-title-main">Metzgeriales</span> Order of liverwort plants

Metzgeriales is an order of liverworts. The group is sometimes called the simple thalloid liverworts: "thalloid" because the members lack structures resembling stems or leaves, and "simple" because their tissues are thin and relatively undifferentiated. All species in the order have a small gametophyte stage and a smaller, relatively short-lived, spore-bearing stage. Although these plants are almost entirely restricted to regions with high humidity or readily available moisture, the group as a whole is widely distributed, and occurs on every continent except Antarctica.

<i>Cavicularia</i> Genus of liverworts

Cavicularia densa is the only species in the liverwort genus Cavicularia. The species was first described in 1897 by Franz Stephani, and is endemic to Japan, where it grows on fine moist soil.

<span class="mw-page-title-main">Treubiaceae</span> Family of liverworts

Treubiaceae is a family of liverworts in the order Treubiales. Species are large and leafy, and were previously classified among the Metzgeriales.

Phycolepidozia exigua is a species of liverwort in the family Cephaloziellaceae. It was thought to be the only species in the genus until a new species from India, Phycolepidozia indica, was found in 2014. Phycolepidozia exigua is endemic to Dominica, where it is critically endangered. Its natural habitat is subtropical or tropical moist lowland forests.

<span class="mw-page-title-main">Blasiales</span> Order of liverworts

Blasiales is an order of liverworts with a single living family and two species. The order has traditionally been classified among the Metzgeriales, but molecular cladistics suggests a placement at the base of the Marchantiopsida.

Apotreubia is a genus of liverworts in the family Treubiaceae. There are two species, Apotreubia nana, which is found in subalpine New Guinea, and Apotreubia pusilla, which has a disjunct distribution between eastern Asia and British Columbia.

<i>Treubia</i> Genus of liverworts

Treubia is a genus of liverworts in the family Treubiaceae. There are seven species, all of which are restricted to the southern hemisphere. Five of the species occur in Australasia and the other occurs in Chile. All species are dioicous, with separate male and female gametophytes.

<i>Makinoa</i> Genus of liverworts

Makinoa crispata is the only species of liverwort in the genus Makinoa and family Makinoaceae. The genus Verdoornia was formerly included in this family, but has been transferred to the family Aneuraceae on the basis of recent cladistic analysis of genetic sequences.

<i>Ptilidium</i> Genus of liverworts

Ptilidium is a genus of liverwort, and is the only genus in family Ptilidiaceae. It includes only three species: Ptilidium californicum, Ptilidium ciliare, and Ptilidium pulcherrimum. The genus is distributed throughout the arctic and subarctic, with disjunct populations in New Zealand and Tierra del Fuego. Molecular analysis suggests that the genus has few close relatives and diverged from other leafy liverworts early in their evolution.

Neotrichocoleaceae is a family of liverworts in order Ptilidiales. It is closely related to the genera Ptilidium and Herzogianthus.

Petalophyllaceae is a family of liverworts in the order Fossombroniales. Most species are thallose; that is, the plant is not differentiated into root, stem, and leaf. The thallus is typically small and bears lamellae on its dorsal surface that give it a ruffled, leafy appearance.

Phymatoceros is the only genus in the hornwort family Phymatocerotaceae and order Phymatocerotales. It includes only two species.

<i>Riella</i> Genus of liverworts

Riella is a genus in the liverwort family Riellaceae, and includes about eighteen species. Plants in the genus are small and grow submerged in shallow temporary pools. Although the genus is widely distributed in the Northern Hemisphere, locating populations is often difficult. Its occurrence is sporadic and local, and the tiny plants are ephemeral. The ornamented spores remain viable for several years, allowing the plants to survive annual drying of their habitat. The plants are easily grown in laboratory cultures.

Petalophyllum, or petalwort, is a genus of liverworts in the order Fossombroniales.

Petalophyllum americanum, common name petalwort, is a species of liverwort in the order Fossombroniales. It is endemic to the Gulf Coast of the United States in Arkansas, Louisiana, Mississippi, and Texas. It was first described as the European species Petalophyllum ralfsii in 1919, but a detailed study later showed that the North American form is a distinct species.

<i>Polytrichastrum formosum</i> Species of moss

Polytrichastrum formosum, commonly known as the bank haircap moss, is a species of moss belonging to the family Polytrichaceae.

<i>Monoclea forsteri</i> Species of liverwort

Monoclea forsteri is one of the two species in the thallose liverwort family Monocleaceae. It is dioicous with the capsule dehiscing with a single longitudinal slit. Endemic and widely distributed throughout New Zealand, it is also the country's largest thalloid liverwort. Hooker described the species in 1820. The holotype is in the British Museum.

References

  1. Heinrichs, Jochen; S. Robbert Gradstein; Rosemary Wilson; Harald Schneider (2005). "Towards a natural classification of liverworts (Marchantiophyta) based on the chloroplast gene rbcL". Cryptogamie Bryologie. 26 (2): 131–150.
  2. He-Nygrén, Xiaolan; Aino Juslén; Inkeri Ahonen; David Glenny; Sinikka Piippo (2006). "Illuminating the evolutionary history of liverworts (Marchantiophyta)—towards a natural classification". Cladistics. 22 (1): 1–31. doi: 10.1111/j.1096-0031.2006.00089.x . PMID   34892891. S2CID   86082381.
  3. Forrest, Laura L.; Christine E. Davis; David G. Long; Barbara J. Crandall-Stotler; Alexandra Clark; Michelle L. Hollingsworth (2006). "Unraveling the evolutionary history of the liverworts (Marchantiophyta): multiple taxa, genomes and analyses". The Bryologist. 109 (3): 303–334. doi:10.1639/0007-2745(2006)109[303:UTEHOT]2.0.CO;2. S2CID   85912159.
  4. Renzaglia, Karen S.; Scott Schuette; R. Joel Duff; Roberto Ligrone; A. Jonathan Shaw; Brent D. Mishler; Jeffrey G. Duckett (2007). "Bryophyte phylogeny: Advancing the molecular and morphological frontiers". The Bryologist. 110 (2): 179–213. doi:10.1639/0007-2745(2007)110[179:BPATMA]2.0.CO;2. S2CID   85788756.
  5. Schuster, Rudolf M. (1992). The Hepaticae and Anthocerotae of North America (Volume 5 ed.). Chicago, Ill.: Field Museum of Natural History. pp. 294–297, 333. ISBN   0-914868-20-9.
  6. Bartholomew-Began, Sharon E. (1991). "A morphogenetic re-evaluation of Haplomitrium Nees (Hepatophyta), Jumgermanniopsida)". Bryophytorum Bibliotheca. 41.
  7. Hébant, C. (1977). "The conducting tissues of bryophytes". Bryophytorum Bibliotheca. 10.
  8. Duckett, Jeffrey G.; Anna Carafa; Roberto Ligrone (2006). "A highly differentiated glomeromycotean association with the mucilage-secreting, primitive antipodean liverwort Treubia: clues to the origins of mycorrhizas". American Journal of Botany. 93 (2): 797–813. doi:10.3732/ajb.93.6.797. PMID   21642142.
  9. Allison, K. W.; John Child (1975). The Liverworts of New Zealand. Dunedin, NZ: University of Otago Press. pp. 232–233.
  10. Schuster, Rudolf M. (1983). "Phytogeography of the Bryophyta". Pages 463-626 in R. M. Schuster (ed.), New Manual of Bryology (Japan: Hattori Botanical Laboratory). ISBN   49381633045 .
  11. Brinda, John C.; Atwood, John J. (eds.). "A Classification of the Haplomitriopsida". The Bryophyte Nomenclator. Retrieved 21 November 2024.

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