Lunularia

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Lunularia
Lunularia cruciata.jpg
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Division: Marchantiophyta
Class: Marchantiopsida
Order: Lunulariales
H.Klinggr.
Family: Lunulariaceae
H.Klinggr.
Genus: Lunularia
Adans.
Species:
L. cruciata
Binomial name
Lunularia cruciata
(L.) Dumort. ex Lindb.
Synonyms
  • SeleniaHill non Nutt.
  • StaurophoraWilldenow
  • DichominumNeck. ex Trevisan
  • MarsiliaKuntze non Linnaeus
  • SedgwickiaBowdich non Wall. & Griff.

Lunularia is a genus of liverworts whose only species is Lunularia cruciata, the crescent-cup liverwort. [1] Lunularia is either the only genus in the order Lunulariales, [2] or may be placed in the order Marchantiales. [3] [4] [5] The name, from Latin luna, moon, refers to the moon-shaped gemma cups.

Contents

Description

Lunularia cruciata grows large, dichotomously branched green thalli with crescent shaped gemma cups containing disc-like gemmae. [6] This is a unique morphological characteristic not possessed by other thalloid liverworts. Its thallus surface is shiny, faintly lined, and is dotted with tiny air pores. When dried the thallus turns yellowish in color and its margin rolls inward. [6]

Lunularia can also reproduce sexually, as illustrated by Haeckel in this drawing of an archegonial head with (diploid) sporophyte plantlets. The main plant body (thallus) is haploid Lunularia cruciata archegonial head with sporophytes from Haeckel Hepaticae.jpg
Lunularia can also reproduce sexually, as illustrated by Haeckel in this drawing of an archegonial head with (diploid) sporophyte plantlets. The main plant body (thallus) is haploid

As in other liverworts, the main plant body or thallus is a haploid gametophyte. The antheridia of L. cruciata develops in early spring, the archegonia develops in spring and sporophytes develop in late summer. [7] However, records of sporophyte developments and sexual reproduction are rare and scattered. This was suspected to have been the result of the anthropogenic spreading of this species, causing a disjunctive distribution of antheridia and archegonia. [7] When reproducing sexually, the four archegonia is arranged in a cross-shaped head (hence the specific name cruciata) bearing diploid sporophyte plantlets. When reproducing asexually, the disc-shaped gemmae are readily dislodged from the cups by splashes of rainwater. They can then quickly "take root" and start to grow in suitably damp places, which is why they are so successful in greenhouses.

Distribution

Lunularia cruciata is distributed across the world, found in continents including Europe, Australasia, Asia, the Americas, and Africa. It occurs commonly in western Europe, and is native to the Mediterranean region, where the morphological forms from sexual reproduction are more frequently found there. [7] It is also common in California, where it now grows "wild", and is known as an introduced weed in gardens and greenhouses in Australia. [8] Ella Orr Campbell believed that L. cruciata was introduced into New Zealand sometime after 1867. [9] The sporophytes of L. cruciata are rare, but has been found in European regions, as well as in South Africa, Argentina, California, India, Japan and New Zealand. [7]

Habitat and ecology

Lunularia cruciata grows in damp, shaded and disturbed habitats such as path and wall edges. [6] It can act as a nutrient indicator because it often grows in alkaline and eutrophic to highly eutrophic soil. [7] Other habitats include loam, boulders, concrete, exposed tree roots, soil covered logs and in the gaps between sidewalk stones. [7] L. cruciata also grows as a horticultural weed in gardens, greenhouses and parks. [7] [6] L. cruciata is sensitive to frost, and is often found near water, where its gemmae are washed ashore. [7]

Chemical properties

Like many other liverwort species, L. cruciata produces a dihydrostilbenoid growth hormone, lunularic acid, that is reported to be a growth inhibitor of liverworts. [10] Cadmium in this liverwort also inhibits gemma germination and apical thallus growth, as well as altering cell and chloroplast structure. [11] Acetone extracts from L. cruciata were tested and showed antibacterial properties, but had no effects against fungal activity. [12]

Related Research Articles

<span class="mw-page-title-main">Moss</span> Division of non-vascular land plants

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.

<span class="mw-page-title-main">Bryophyte</span> Terrestrial plants that lack vascular tissue

Bryophytes are a group of land plants (embryophytes), sometimes treated as a taxonomic division, that contains three groups of non-vascular land plants: the liverworts, hornworts, and mosses. In the strict sense, the division Bryophyta consists of the mosses only. Bryophytes are characteristically limited in size and prefer moist habitats although some species 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.

<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.

<span class="mw-page-title-main">Hornwort</span> Division of non-vascular land plants with horn-shaped sporophytes

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.

<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.

<i>Marchantia</i> Genus of plants in the liverwort family Marchantiaceae

Marchantia is a genus of liverworts in the family Marchantiaceae and the order Marchantiales.

<i>Marchantia quadrata</i> Species of liverwort

Marchantia quadrata is a species of liverwort, a simple non-flowering plant that grows as a flat, green, leaf-like structure (thallus) typically found on damp rocks and soil along stream banks in the Northern Hemisphere. The species was originally classified in its own genus Preissia due to its distinctive features, including larger spores and lack of the specialised cup-like reproductive structures common in other liverworts, but genetic studies have shown it belongs within the genus Marchantia. Like most liverworts, it reproduces both sexually, through separate male and female plants that produce umbrella-like reproductive structures, and through regeneration from fragments. The species prefers slightly drier habitats than its relatives and shows significant genetic variation across its range, suggesting it may comprise several distinct but closely related species.

<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>Conocephalum</i> Genus of plants

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.

Monoicy is a sexual system in haploid plants where both sperm and eggs are produced on the same gametophyte, in contrast with dioicy, where each gametophyte produces only sperm or eggs but never both. Both monoicous and dioicous gametophytes produce gametes in gametangia by mitosis rather than meiosis, so that sperm and eggs are genetically identical with their parent gametophyte.

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.

<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.

<i>Marchantia polymorpha</i> Species of liverwort

Marchantia polymorpha is a species of large thalloid liverwort in the class Marchantiopsida. M. polymorpha is highly variable in appearance and contains several subspecies. This species is dioicous, having separate male and female plants. M. polymorpha has a wide distribution and is found worldwide. Common names include common liverwort or umbrella liverwort.

<i>Pellia epiphylla</i> Species of liverworts in the family Pelliaceae

Pellia epiphylla is a species of thallose liverwort. It occurs in North America, Europe, North Africa and parts of Asia. It grows in patches in damp, sheltered places on neutral or acidic substrates. It is common on the banks of rivers, streams and ditches and also grows in wet woodland, marshes and on wet rocks.

<i>Sphaerocarpos texanus</i> Species of liverwort

Sphaerocarpos texanus, the Texas balloonwort, is a species of liverwort in the Sphaerocarpaceae family, found in the Americas, northern Africa and Europe.

<i>Tetraphis pellucida</i> Species of moss

Tetraphis pellucida, the pellucid four-tooth moss, is one of two species of moss in the acrocarpous genus Tetraphis. Its name refers to its four large peristome teeth found on the sporophyte capsule.

<i>Metzgeria furcata</i> Species of liverwort

Metzgeria furcata, the forked veilwort, is a frequent liverwort growing on the bark of a wide range of tree and shrub species and occasionally on rocks. It is a slim, translucent thallose liverwort that forms yellow-green mats of branches about 1mm wide.

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

<i>Asterella californica</i> Species of plant

Asterella californica is a complex thallic liverwort in the phylum Marchantiophyta. A. californica often grows as colonies of flat rosettes of light green, rigid thalli, with undersides dark wine-red to nearly black. The receptacles are rounded, with four lobes each bearing a single sporangium sheathed by a white tattered skirt. A. californica is dioecious with separate male plants often intermingled with female plants. This species is found throughout California. See Distribution information below. Asterella californica is the commonest species of the three species of Asterella occurring in California; the other two species are A. bolanderi and A. palmeri.

<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

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  2. Söderström; et al. (2016). "World checklist of hornworts and liverworts". PhytoKeys (59): 1–826. doi: 10.3897/phytokeys.59.6261 . PMC   4758082 . PMID   26929706.
  3. Flores, Jorge R.; Catalano, Santiago A.; Muñoz, Jesus; Suárez, Guillermo M. (2018). "Combined phylogenetic analysis of the subclass Marchantiidae (Marchantiophyta): towards a robustly diagnosed classification". Cladistics. 34 (5): 517–541. doi:10.1111/cla.12225. hdl: 10261/248464 . PMID   34706484. S2CID   52831959.
  4. Flores, Jorge R.; Bippus, Alexander C.; Suárez, Guillermo M.; Hyvönen, Jaakko (2020). "Defying death: incorporating fossils into the phylogeny of the complex thalloid liverworts (Marchantiidae, Marchantiophyta) confirms high order clades but reveals discrepancies in family-level relationships". Cladistics. 37 (3): 231–247. doi:10.1111/cla.12442. ISSN   1096-0031. PMID   34478198. S2CID   225165843.
  5. Cole, Theodor C. H.; Hilger, Hartmut H.; Goffinet, Bernard (2019-05-24). "Bryophyte Phylogeny Poster (BPP)". PeerJ Preprints. doi: 10.7287/peerj.preprints.27571v3 . S2CID   196666379.
  6. 1 2 3 4 "Crescent-cup Liverwort | NatureSpot". www.naturespot.org.uk. Retrieved 2022-04-05.
  7. 1 2 3 4 5 6 7 8 Kirschner R., Nebel M. & Butterfass T. (2010). "Observations on fertile populations of Lunularia cruciata (L.) Dumort. ex Lindb. (Marchantiopsida: Lunulariaceae) in Germany" (PDF). Stuttgarter Beiträge Naturkunde Serie A [Biologie]. NS_3_A: 363–371.
  8. Schuster, Rudolf M. The Hepaticae and Anthocerotae of North America, volume VI, pages 80-91. (Chicago: Field Museum of Natural History, 1992). ISBN   0-914868-21-7.
  9. Campbell, Ella O. (1965). "Lunularia in New Zealand". Tuatara. 13 (1): 31–41. Retrieved 27 May 2016.
  10. Lunularic acid, a common endogenous growth inhibitor of liverworts. R. J. Pryce, Planta, 1971, Volume 97, Number 4, pages 354-357, doi : 10.1007/BF00390214
  11. Carginale, V.; Sorbo, S.; Capasso, C.; Trinchella, F.; Cafiero, G.; Basile, A. (2004-03-01). "Accumulation, localisation, and toxic effects of cadmium in the liverwort Lunularia cruciata". Protoplasma. 223 (1): 53–61. doi:10.1007/s00709-003-0028-0. ISSN   0033-183X. PMID   15004743. S2CID   25486711.
  12. Basile, Adriana; Giordano, Simonetta; Sorbo, Sergio; Vuotto, Maria Luisa; Ielpo, Maria Teresa Lucia; Castaldo Cobianchi, Rosa (January 1998). "Antibiotic Effects of Lunularia cruciata (Bryophyta) Extract". Pharmaceutical Biology. 36 (1): 25–28. doi: 10.1076/phbi.36.1.25.4612 . ISSN   1388-0209.