Marchantiophyta6 Maret 2010 pukul 04:26 | Ditulis dalam Uncategorized | Tinggalkan komentar
Marchantiophyta [mɑː(r)ˌkæntiˈɑːfɪtə] (help·info) are a division of bryophyte plants commonly referred to as hepatics or liverworts. Like other bryopeos, 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 6000 to 8000 species of liverworts, though when Neotropical regions are better studied this number may approach 10,000. 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.
Most liverworts are small, usually from 2–20 millimetres (0.08–0.8 in) wide with individual plants less than 10 centimetres (4 in) long, 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 three or more ranks, the middle rank being conspicuously different from the outer ranks; these are called leafy liverworts or scale liverworts. (See the gallery below for examples.)
Liverworts can most reliably be distinguished from the apparently similar mosses by their single-celled rhizoids. Other differences are not universal for all mosses and all liverworts; 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. In addition, 90% of liverworts contain oil bodies in at least some of their cells, and these cellular structures are absent from most other bryophytes and from all vascular plants. 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. 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. 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. Even in other bryophytes, the sporophyte is persistent and disperses spores over an extended period.
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. 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). 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 dioicious liverworts, female and male sex organs are borne on different and separate gametophyte plants. In monoicious liverworts, the two kinds of reproductive structures are borne on different branches of the same plant. In either case, the sperm must swim 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 aid in propulsion. Their journey is further assisted either by the splashing of raindrops or the presence of a thin layer of water covering the plants. Without water, the journey from antheridium to archegonium cannot occur.
In the presence of such water, sperm from the antheridia swim to the archegonia and 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. 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.
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. As with most groups of living plants, they are most common (both in numbers and species) in moist tropical areas. Liverworts are more commonly found in moderate to deep shade, though desert species may tolerate direct sunlight and periods of total desiccation.
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). However, since this grouping makes the Bryophyta paraphyletic, the liverworts are now usually given their own division. The use of the division name Bryophyta sensu latu is still found in the literature, but more frequently the Bryophyta now is used in a restricted sense to include only the mosses.
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. Among the earliest fossils believed to be liverworts are compression fossils of Pallaviciniites from the Upper Devonian of New York. These fossils resemble modern species in the Metzgeriales. 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, USA.
Bryologists classify liverworts in the division Marchantiophyta. This divisional name is based on the name of the most universally recognized liverwort genus Marchantia. 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, 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, the Marchantiophyta may be subdivided into three classes:
- The Jungermanniopsida includes the two orders Metzgeriales (simple thalloids) and Jungermanniales (leafy liverworts).
- The Marchantiopsida includes the three orders Marchantiales (complex-thallus liverworts), and Sphaerocarpales (bottle hepatics), as well as the Blasiales (previously placed among the Metzgeriales). It also includes the problematic genus Monoclea, which is sometimes placed in its own order Monocleales.
- A third class, the Haplomitriopsida is newly recognized as a basal sister group to the other liverworts; it comprises the genera Haplomitrium, Treubia, and Apotreubia.
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.
It is estimated that there are 6000 to 8000 species of liverworts, at least 85% of which belong to the leafy group.
In ancient times, it was believed that liverworts cured diseases of the liver, hence the name. In Old English, the word liverwort literally means liver plant. 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”.
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 aquaria. Their thin, slender branches float on the water’s surface and provide habitat for both small invertebrates and the fish that feed on them.