Marchantia polymorpha | |
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Scientific classification | |
Kingdom: | Plantae |
Division: | Marchantiophyta |
Class: | Marchantiopsida |
Order: | Marchantiales |
Family: | Marchantiaceae |
Genus: | Marchantia |
Species: | M. polymorpha |
Binomial name | |
Marchantia polymorpha | |
Synonyms | |
Marchantia alpestris |
Marchantia polymorpha is a species of large thalloid liverwort in the class Marchantiopsida. [1] M. polymorpha is highly variable in appearance and contains several subspecies. [2] This species is dioicous, having separate male and female plants. [2] M. polymorpha has a wide distribution and is found worldwide. [3] Common names include common liverwort or umbrella liverwort. [2]
Marchantia polymorpha subsp. ruderalis has a circumpolar boreo-arctic cosmopolitan distribution, found worldwide on all continents except Antarctica. [4]
Marchantia polymorpha grows on shaded moist soil and rocks in damp habitats such as the banks of streams and pools, bogs, fens and dune slacks. [1] While most varieties grow on moist substrates, Marchantia polymorpha var. aquatica is semi-aquatic and is often found invading marshes, as well as small ponds that do not have a consistent water table. [3]
The species often grows in man-made habitats such as gardens, paths and greenhouses and can be a horticultural weed. One method of spread is in the production and sale of liners. Liners infested with M. polymorpha, often in association with silvery thread moss, are commonly grown in one region of the country, transported to another region to continue growth, and are shipped to a retail location before being planted. Plants have the potential to pick up or disperse these species at each point of transfer. [5]
Marchantia polymorpha is known to be able to use artificial light to grow in places which are otherwise devoid of natural light. A study from Niagara Cave showed that under such conditions, Marchantia polymorpha was able to produce gemmae, indicating that the plant could be able to reproduce in illuminated caves. [6] It has also been reported from Crystal Cave in Wisconsin. [7]
An important benefit of M. polymorpha is that it is frequently the first vegetation to appear after a large wildfire. Exposed mineral soil and high lime concentrations present after a severe fire provide favorable conditions for gametophyte establishment. After invading the burned area, M. polymorpha grows rapidly, sometimes covering the entire site. This is important to the prevention of soil erosion that frequently occurs after severe fires, causing significant, long-term, environmental damage.
In addition, M. polymorpha renews the humus in the burned soil, and over time raises the quality of the soil to a point where other vegetation can be established. [3] Not only does common liverwort secure burned soil and improve its quality, but after a certain point, when the soil health is restored, it can no longer compete with the vegetation that originally inhabited the area.
In a USDA study in northeastern Minnesota, M. polymorpha dominated the landscape for 3 years after a severe fire, but after 5 years was replaced by lichen. After a similar fire in New Jersey M. polymorpha covered the ground for 2–3 years, but was then replaced with local shrubs and forbs. In Alaska the following vegetative successions were observed after a fire, again indicating that after soil rehabilitation has occurred the original flora returns and outcompetes M. polymorpha. [3]
It is a thallose liverwort which forms a rosette of flattened thalli with forked branches. The thalli grow up to 10cm long with a width of up to 2cm. It is usually green in colour but older plants can become brown or purplish. The upper surface has a pattern of polygonal markings. The underside is covered by many root-like rhizoids which attach the plant to the soil. [2] The complex oil bodies in Marchantia polymorpha, as in all Marchantiopsida species, are restricted to specialized cells where they occupy nearly the entire intracellular space. [8]
The life cycle has an alternation of generations. Haploid gametophytes produces haploid gametes, egg and sperm, which then fuse to form a diploid zygote. The zygote later develops into a sporophyte which later produces haploid spores through meiosis.
The plants produce umbrella-like reproductive structures known as gametangiophores. The gametangiophores of female plants (also known as archegoniophores) consist of a stalk with star-like rays at the top. These contain archegonia, the organs which produce the ova. Male gametangiophores (also known as antheridiophores) are topped by a flattened disc containing the antheridia which produce sperm. [2] [9]
This species reproduces asexually by gemmae that are produced within gemma cups. Gemmae are lentil shaped and are released by droplets of water. Plants produced in this way can expand a patch significantly. [2]
The U.S. Department of Agriculture has studied M. polymorpha for its use in rehabilitating disturbed sites due to its ability to tolerate high lead concentrations in soils, along with other heavy metals. In turn, M. polymorpha colonies can be an indication that a site has high concentrations of heavy metals, especially when found in dense mats with little other vegetative species present. [3] A study from Loja city in tropical Ecuador found that, when growing in an urban setting, M. polymorpha bioaccumulated four heavy metals, aluminium, copper, iron and zinc. [10]
It has historically been thought to remedy liver ailments because of its perceived similarities to the shape and texture of animal livers. [11] This is an example of the doctrine of signatures.
Marchantia polymorpha produces the antifungal bis[bibenzyls] dihydrostilbenoids plagiochin E, 13,13'-O-isoproylidenericcardin D, riccardin H, marchantin E, neomarchantin A, marchantin A and marchantin B. Its strong fungicidal capability has been used successfully in the treatment of skin and nail fungi. [12]
A gametophyte is one of the two alternating multicellular phases in the life cycles of plants and algae. It is a haploid multicellular organism that develops from a haploid spore that has one set of chromosomes. The gametophyte is the sexual phase in the life cycle of plants and algae. It develops sex organs that produce gametes, haploid sex cells that participate in fertilization to form a diploid zygote which has a double set of chromosomes. Cell division of the zygote results in a new diploid multicellular organism, the second stage in the life cycle known as the sporophyte. The sporophyte can produce haploid spores by meiosis that on germination produce a new generation of gametophytes.
Mosses are small, non-vascular flowerless plants in the taxonomic division Bryophytasensu stricto. Bryophyta may also refer to the parent group bryophytes, which comprise liverworts, mosses, and hornworts. Mosses typically form dense green clumps or mats, often in damp or shady locations. The individual plants are usually composed of simple leaves that are generally only one cell thick, attached to a stem that may be branched or unbranched and has only a limited role in conducting water and nutrients. Although some species have conducting tissues, these are generally poorly developed and structurally different from similar tissue found in vascular plants. Mosses do not have seeds and after fertilisation develop sporophytes with unbranched stalks topped with single capsules containing spores. They are typically 0.2–10 cm (0.1–3.9 in) tall, though some species are much larger. Dawsonia, the tallest moss in the world, can grow to 50 cm (20 in) in height. There are approximately 12,000 species.
Bryophytes are a group of land plants, sometimes treated as a taxonomic division, that contains three groups of non-vascular land plants (embryophytes): the liverworts, hornworts, and mosses. In the strict sense, Bryophyta consists of the mosses only. Bryophytes are characteristically limited in size and prefer moist habitats although they can survive in drier environments. The bryophytes consist of about 20,000 plant species. Bryophytes produce enclosed reproductive structures, but they do not produce flowers or seeds. They reproduce sexually by spores and asexually by fragmentation or the production of gemmae. Though bryophytes were considered a paraphyletic group in recent years, almost all of the most recent phylogenetic evidence supports the monophyly of this group, as originally classified by Wilhelm Schimper in 1879. The term bryophyte comes from Ancient Greek βρύον (brúon) 'tree moss, liverwort', and φυτόν (phutón) 'plant'.
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.
A sporophyte is the diploid multicellular stage in the life cycle of a plant or alga which produces asexual spores. This stage alternates with a multicellular haploid gametophyte phase.
Hornworts are a group of non-vascular Embryophytes constituting the division Anthocerotophyta. The common name refers to the elongated horn-like structure, which is the sporophyte. As in mosses and liverworts, hornworts have a gametophyte-dominant life cycle, in which cells of the plant carry only a single set of genetic information; the flattened, green plant body of a hornwort is the gametophyte stage of the plant.
Non-vascular plants are plants without a vascular system consisting of xylem and phloem. Instead, they may possess simpler tissues that have specialized functions for the internal transport of water.
An antheridium is a haploid structure or organ producing and containing male gametes. The plural form is antheridia, and a structure containing one or more antheridia is called an androecium. Androecium is also the collective term for the stamens of flowering plants.
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.
A gemma is a single cell, or a mass of cells, or a modified bud of tissue, that detaches from the parent and develops into a new individual. This type of asexual reproduction is referred to as fragmentation. It is a means of asexual propagation in plants. These structures are commonly found in fungi, algae, liverworts and mosses, but also in some flowering plants such as pygmy sundews and some species of butterworts. Vascular plants have many other methods of asexual reproduction including bulbils and turions.
Marchantia is a genus of liverworts in the family Marchantiaceae and the order Marchantiales.
Lunularia is a genus of liverworts whose only species is Lunularia cruciata, the crescent-cup liverwort. Lunularia is either the only genus in the order Lunulariales, or may be placed in the order Marchantiales. The name, from Latin luna, moon, refers to the moon-shaped gemma cups.
Conocephalum is a genus of complex thalloid liverworts in the order Marchantiales and is the only extant genus in the family Conocephalaceae. Some species of Conocephalum are assigned to the Conocephalum conicum complex, which includes several cryptic species. Conocephalum species are large liverworts with distinct patterns on the upper thallus, giving the appearance of snakeskin. The species Conocephalum conicum is named for its cone-shaped reproductive structures, called archegoniophores. Common names include snakeskin liverwort, great scented liverwort and cat-tongue liverwort.
A prothallus, or prothallium, is usually the gametophyte stage in the life of a fern or other pteridophyte. Occasionally the term is also used to describe the young gametophyte of a liverwort or peat moss as well. In lichens it refers to the region of the thallus that is free of algae.
Plant reproduction is the production of new offspring in plants, which can be accomplished by sexual or asexual reproduction. Sexual reproduction produces offspring by the fusion of gametes, resulting in offspring genetically different from either parent. Asexual reproduction produces new individuals without the fusion of gametes, resulting in clonal plants that are genetically identical to the parent plant and each other, unless mutations occur.
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.
Conocephalum conicum, also known as the great scented liverwort or snakeskin liverwort, is a liverwort species in the genus Conocephalum. C. conicum is part of the Conocephalum conicum complex, which includes several cryptic species. The name C. conicum refers to the cone-shaped archegoniophore, which bear sporangia.
Marchantia berteroana is a liverwort species in the genus Marchantia.
Tortula muralis, commonly known as wall-screw moss, is a species of moss in the family Pottiaceae. T. muralis is found throughout the world.
The oil bodies of liverworts, occasionally dubbed complex oil bodies for distinction, are unique organelles exclusive to the Marchantiophyta. They are markedly different from the oil bodies found in other land plants and algae in that they are membrane-bound, and not associated with food storage. The organelles are variable and present in an estimated 90% of liverwort species, often proving taxonomically relevant. As a whole, the formation and function of the organelles are poorly understood. Complex oil bodies are recognized as sites of isoprenoid biosynthesis and essential oil accumulation, and have been implicated with anti-herbivory, desiccation tolerance, and photo-protection.