Cavicularia

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Cavicularia
Cavicularia densa - National Museum of Nature and Science, Tokyo - DSC06835.JPG
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Division: Marchantiophyta
Class: Marchantiopsida
Order: Blasiales
Family: Blasiaceae
Genus: Cavicularia
Steph. 1897 [1]
Species:
C. densa
Binomial name
Cavicularia densa
Steph. 1897 [1]

Cavicularia densa is the only species in the liverwort genus Cavicularia. The species was first described in 1897 by Franz Stephani, [2] and is endemic to Japan, [3] [4] where it grows on fine moist soil. [5]

Contents

Plants are thalloid and flattened, with distinct upper and lower surfaces and a faint central strand. [3] Thin scales grow from the underside in two rows, and in the region between the scales and the central strand are small ear-shaped domatia which harbor colonies of the blue-green alga Nostoc . [3] The plants are dioicous, with the male antheridia and female archegonia produced by separate plants. [3] Plants may also reproduce asexually from multicellular gemmae produced in crescent-shaped receptacles on the thallus surface. [6]

The spores are spherical and apolar, with a surface devoid of ornamentation except for tiny papillae. [7] Gametophyte development is endosporic, so that cell divisions begin inside the spore wall. [5] This pattern of development is normally found in liverworts from xeric environments, rather than those growing in moist habitats like Cavicularia. [5] Once the young gametophyte germinates and ruptures the spore coat, it produces a multi-layered mass from which the adult plant will develop. [7]

Cavicularia is classified in the family Blasiaceae along with the genus Blasia , [8] from which it is distinguished by the absence of a collar around the base of the sporophyte capsule, and a clustered arrangement of sperm-producing antheridia. Like Blasia, plants of Cavicularia possess domatia containing colonies of the blue-green alga Nostoc . [7] [3] Despite their similarities and traditional classification together, the two genera do not group together as a clade in some recent analyses. While Blasia attaches to the base of the complex-thalloid clade Marchantiopsida, Cavicularia lies at the base of the simple-thalloid and leafy clade Jungermanniopsida. [9] Thus, the genus has been dubbed "problematic", but modifications to its taxonomic placement await further investigation. [9]

The chemical compound cavicularin was isolated from this species. Cavicularin is notable for being the first compound isolated from nature displaying optical activity solely due to the presence of planar chirality and axial chirality.

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.

<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>Lunularia</i> Species of liverwort

Lunularia cruciata, the crescent-cup liverwort, is a liverwort of the order Marchantiales, and the only species in the genus Lunularia and family Lunulariaceae. The name, from Latin luna, moon, refers to the moon-shaped gemma cups.

<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>Takakia</i> Genus of mosses

Takakia is a genus of two species of mosses known from western North America and central and eastern Asia. The genus is placed as a separate family, order and class among the mosses. It has had a history of uncertain placement, but the discovery of sporophytes clearly of the moss-type firmly supports placement with the mosses.

<i>Dendroceros</i> Genus of hornworts

Dendroceros is a genus of hornworts in the family Dendrocerotaceae. The genus contains about 51 species native to tropical and sub-tropical regions of the world.

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

Jungermanniopsida is the largest of three classes within the division Marchantiophyta (liverworts).

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.

<i>Buxbaumia</i> Genus of mosses

Buxbaumia is a genus of twelve species of moss (Bryophyta). It was first named in 1742 by Albrecht von Haller and later brought into modern botanical nomenclature in 1801 by Johann Hedwig to commemorate Johann Christian Buxbaum, a German physician and botanist who discovered the moss in 1712 at the mouth of the Volga River. The moss is microscopic for most of its existence, and plants are noticeable only after they begin to produce their reproductive structures. The asymmetrical spore capsule has a distinctive shape and structure, some features of which appear to be transitional from those in primitive mosses to most modern mosses.

<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.

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

Haplomitriopsida is a newly recognized 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. The group thus provides a unique insight into the early evolution of liverworts in particular and of land plants in general.

<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.

<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>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.

<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.

Dioicy is a sexual system where archegonia and antheridia are produced on separate gametophytes. It is one of the two main sexual systems in bryophytes, the other being monoicy. Both dioicous and monoicous gametophytes produce gametes in gametangia by mitosis rather than meiosis, so that sperm and eggs are genetically identical with their parent gametophyte.

<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. 1 2 Stephani, Franz (1897). "Hepaticae japonicae". Bulletin de l'Herbier Boissier . Sér. 2. 5: 76–108.
  2. Grolle, Riclef (1983). "Nomina generica Hepaticarum; references, types and synonymies". Acta Botanica Fennica. 121: 1–62.
  3. 1 2 3 4 5 Schuster, Rudolf M. (1992). The Hepaticae and Anthocerotae of North America. Vol. V. Chicago: Field Museum of Natural History. pp. 287–354. ISBN   0-914868-20-9.
  4. Tan, Benito C.; Pócs, Tamás (2000). "Bryogeography and conservation of bryophytes". In A. Jonathan Shaw; Bernard Goffinet (eds.). Bryophyte Biology. Cambridge: Cambridge University Press. pp. 403–448. ISBN   0-521-66097-1.
  5. 1 2 3 Nehira, Kunito (1987). "Some ecological correlations of spore germination patterns in liverworts". The Bryologist. 90 (4): 405–408. doi:10.2307/3243106. JSTOR   3243106.
  6. Inoue, Hiroshi (1976). Illustrations of Japanese Hepaticae. Vol. 2. Tokyo.{{cite book}}: CS1 maint: location missing publisher (link)
  7. 1 2 3 Schofield, W. B. (1985). Introduction to Bryology. New York: Macmillan. pp. 182–184, 190. ISBN   0-02-949660-8.
  8. Crandall-Stotler, Barbara; Raymond E. Stotler (2000). "Morphology and classification of the Marchantiophyta". In A. Jonathan Shaw; Bernard Goffinet (eds.). Bryophyte Biology. Cambridge: Cambridge University Press. pp. 21–70. ISBN   0-521-66097-1.
  9. 1 2 Forrest, Laura L.; Barbara J. Crandall-Stotler (2004). "A Phylogeny of the Simple Thalloid Liverworts (Jungermanniopsida, Metzgeriidae) as Inferred from Five Chloroplast Genes". Monographs in Systematic Botany. Molecular Systematics of Bryophytes. Missouri Botanical Garden Press. 98: 119–140.

Further reading