Dawsonia (plant)

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Dawsonia
Dawsonia superba 2.jpg
Dawsonia superba in Abel Tasman National Park, New Zealand
Scientific classification Red Pencil Icon.png
Kingdom: Plantae
Division: Bryophyta
Class: Polytrichopsida
Order: Polytrichales
Family: Polytrichaceae
Genus: Dawsonia
R.Br., 1811 [1]
Species

Dawsonia is a genus of acrocarpous mosses. Dawsonia, along with other members of the order Polytrichales, are taller than most mosses and have thicker leaves. Their sporophytes have conducting systems analogous to those of vascular plants. Dawsonia superba is found in New Zealand, Australia and New Guinea. [2] D. longifolia is found in the Philippines, Indonesia, Malaysia, and Australia. [3] [4] [5] There is uncertainty as to whether D. superba and D. longifolia are actually distinct species.

Contents

Etymology

Dawsonia was named in honor of Dawson Turner (1775–1858), distinguished cryptogamist and friend of Robert Brown, who named the genus in 1811. [1]

Description

Height

Moss gametophytes lack internal transport tissues, which, coupled with the absence of cuticles, leads to the water-loss characteristic of bryophytes. As bryophytes can only grow when hydrated, the lack of conducting tissue restricts most mosses, even in relatively wet habitats, to a low stature.

However, Dawsonia (along with other genera in the Polytrichales order) reaches heights comparable to those of vascular plants. Polytrichales are acrocarpous mosses – they have vertical stems with terminal reproductive structures, with the sporophyte growing vertically (along the same axis as the gametophyte stem).

The tallest moss in the world is D. superba, which can have a stem up to 50 centimetres (20 in) tall. [2]

Leaves

The leaves of Polytrichum and Dawsonia (and related moss) differ from those of most mosses, which are only one or two cells thick. The Polytrichaceae have lamellae – upright sheets of small, photosynthetic cells on the upper surface of the leaves with a function analogous to the mesophyll cells of vascular plant leaves. They increase the surface area of cell walls available for CO2 uptake, while at the same time maintaining layers of moist air between lamellae, reducing water loss. Lamella margins have a surface wax layer which prevents water from flooding into the interlamellar spaces.

Stems

Section of a Dawsonia stem. The cylinder of hydrome can be seen in the centre, and a ring of leaf traces can be seen outside the cylinder Dawsonia stem.jpg
Section of a Dawsonia stem. The cylinder of hydrome can be seen in the centre, and a ring of leaf traces can be seen outside the cylinder

The stems of Polytrichales have conducting systems which are analogous to the xylem and phloem of vascular plants. The water-conducting tissue is the hydrome, made up of elongated cells known as hydroids. Unlike the xylem of vascular plants, there is no secondary thickening of cell walls, as bryophytes lack lignin. The phloem analogue in Polytrichales is the leptome, made up of leptoids, they are similar to sieve cells. Hydrome and leptome are well-developed in Polytrichales, and also appear in a number of other bryophytes.

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Plant cell Type of eukaryotic cell present in green plants

Plant cells are eukaryotic cells present in green plants, photosynthetic eukaryotes of the kingdom Plantae. Their distinctive features include primary cell walls containing cellulose, hemicelluloses and pectin, the presence of plastids with the capability to perform photosynthesis and store starch, a large vacuole that regulates turgor pressure, the absence of flagella or centrioles, except in the gametes, and a unique method of cell division involving the formation of a cell plate or phragmoplast that separates the new daughter cells.

Vascular plant Clade of land plants with xylem and phloem

Vascular plants, also called tracheophytes or collectively Tracheophyta, form a large group of land plants that have lignified tissues for conducting water and minerals throughout the plant. They also have a specialized non-lignified tissue to conduct products of photosynthesis. Vascular plants include the clubmosses, horsetails, ferns, gymnosperms and angiosperms. Scientific names for the group include Tracheophyta, Tracheobionta and Equisetopsida sensu lato. Some early land plants had less developed vascular tissue; the term eutracheophyte has been used for all other vascular plants, including all living ones.

Tissue (biology) Group of cells having similar appearance and performing the same function

In biology, tissue is a biological organizational level between cells and a complete organ. A tissue is an ensemble of similar cells and their extracellular matrix from the same origin that together carry out a specific function. Organs are then formed by the functional grouping together of multiple tissues.

Moss 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.

Bryophyte Terrestrial plants that lack vascular tissue

Bryophytes are a proposed taxonomic division containing three groups of non-vascular land plants (embryophytes): the liverworts, hornworts and mosses. They 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'.

Embryophyte Subclade of green plants, also known as land plants

The Embryophyta, or land plants, are the most familiar group of green plants that comprise vegetation on Earth. Embryophyta is a clade within the Phragmoplastophyta, a larger clade that also includes several groups of green algae including the Charophyceae and Coleochaetales. Within this larger clade the embryophytes are sister to the Zygnematophyceae/Mesotaeniaceae and consist of the bryophytes plus the polysporangiophytes. Living embryophytes therefore include hornworts, liverworts, mosses, lycophytes, ferns, gymnosperms and flowering plants.

Non-vascular plant Plant without a vascular system

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.

A hydroid is a type of vascular cell that occurs in certain bryophytes. In some mosses such as members of the Polytrichaceae family, hydroids form the innermost layer of cells in the stem. At maturity they are long, colourless, thin walled cells of small diameter, containing water but no living protoplasm. Collectively, hydroids function as a conducting tissue, known as the hydrome, transporting water and minerals drawn from the soil. They are surrounded by bundles of living cells known as leptoids which carry sugars and other nutrients in solution. The hydroids are analogous to the tracheids of vascular plants but there is no lignin present in the cell walls to provide structural support.

<i>Cooksonia</i> Group of vascular land plants (extinct)

Cooksonia is an extinct group of primitive land plants, treated as a genus, although probably not monophyletic. The earliest Cooksonia date from the middle of the Silurian ; the group continued to be an important component of the flora until the end of the Early Devonian, a total time span of 433 to 393 million years ago. While Cooksonia fossils are distributed globally, most type specimens come from Britain, where they were first discovered in 1937. Cooksonia includes the oldest known plant to have a stem with vascular tissue and is thus a transitional form between the primitive non-vascular bryophytes and the vascular plants.

Vascular tissue Conducting tissue in vascular plants

Vascular tissue is a complex conducting tissue, formed of more than one cell type, found in vascular plants. The primary components of vascular tissue are the xylem and phloem. These two tissues transport fluid and nutrients internally. There are also two meristems associated with vascular tissue: the vascular cambium and the cork cambium. All the vascular tissues within a particular plant together constitute the vascular tissue system of that plant.

<i>Polytrichum commune</i> Species of moss

Polytrichum commune is a species of moss found in many regions with high humidity and rainfall. The species can be exceptionally tall for a moss with stems often exceeding 30 cm (12 in) though rarely reaching 70 cm (27.5 in), but it is most commonly found at shorter lengths of 5 to 10 cm. It is widely distributed throughout temperate and boreal latitudes in the Northern Hemisphere and also found in Mexico, several Pacific Islands including New Zealand, and also in Australia. It typically grows in bogs, wet heathland and along forest streams.

Plant cuticle Waterproof covering of aerial plant organs

A plant cuticle is a protecting film covering the epidermis of leaves, young shoots and other aerial plant organs without periderm. It consists of lipid and hydrocarbon polymers impregnated with wax, and is synthesized exclusively by the epidermal cells.

A leptoid is a type of elongated food-conducting cell like phloem in the stems of some mosses, such as the family Polytrichaceae. They surround strands of water-conducting hydroids. They have some structural and developmental similarities to the sieve elements of seedless vascular plants. At maturity they have inclined end cell walls with small pores and degenerate nuclei. The conduction cells of mosses, leptoids and hydroids, appear similar to those of fossil protracheophytes. However they're not thought to represent an intermediate stage in the evolution of plant vascular tissues but to have had an independent evolutionary origin.

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. The resulting clonal plants are genetically identical to the parent plant and each other, unless mutations occur.

Polysporangiophyte Spore-bearing plants with branched sporophytes

Polysporangiophytes, also called polysporangiates or formally Polysporangiophyta, are plants in which the spore-bearing generation (sporophyte) has branching stems (axes) that bear sporangia. The name literally means 'many sporangia plant'. The clade includes all land plants (embryophytes) except for the bryophytes whose sporophytes are normally unbranched, even if a few exceptional cases occur. While the definition is independent of the presence of vascular tissue, all living polysporangiophytes also have vascular tissue, i.e., are vascular plants or tracheophytes. Extinct polysporangiophytes are known that have no vascular tissue and so are not tracheophytes.

<i>Aglaophyton</i> Extinct (Devonian) prevascular land plant

Aglaophyton major was the sporophyte generation of a diplohaplontic, pre-vascular, axial, free-sporing land plant of the Lower Devonian. It had anatomical features intermediate between those of the bryophytes and vascular plants or tracheophytes.

Lepidodendrales Extinct order of vascular tree-like plants

Lepidodendrales were primitive, vascular, arborescent (tree-like) plants related to the lycopsids. Members of Lepidodendrales are the best understood of the fossil lycopsids due to the vast diversity of Lepidodendrales specimens and the diversity in which they were preserved; the extensive distribution of Lepidodendrales specimens as well as their well-preservedness lends paleobotanists exceptionally detailed knowledge of the coal-swamp giants’ reproductive biology, vegetative development, and role in their paleoecosystem. The defining characteristics of the Lepidodendrales are their secondary xylem, extensive periderm development, three-zoned cortex, rootlike appendages known as stigmarian rootlets arranged in a spiralling pattern, and megasporangium each containing a single functional megaspore that germinates inside the sporangium. Many of these different plant organs have been assigned both generic and specific names as relatively few have been found organically attached to each other. Some specimens have been discovered which indicate heights of 40 and even 50 meters and diameters of over 2 meters at the base. The massive trunks of some species branched profusely, producing large crowns of leafy twigs; though some leaves were up to 1 meter long, most were much shorter, and when leaves dropped from branches their conspicuous leaf bases remained on the surface of branches. Strobili could be found at the tips of distal branches or in an area at the top of the main trunk. The underground organs of Lepidodendrales typically consisted of dichotomizing axes bearing helically arranged, lateral appendages serving an equivalent function to roots. Sometimes called "giant club mosses", they are believed to be more closely related to extant quillworts based on xylem, although fossil specimens of extinct Selaginellales from the Late Carboniferous also had secondary xylem.

<i>Polytrichum</i> Genus of mosses in the family Polytrichaceae

Polytrichum is a genus of mosses — commonly called haircap moss or hair moss — which contains approximately 70 species that cover a cosmopolitan distribution. The genus Polytrichum has a number of closely related sporophytic characters. The scientific name is derived from the Ancient Greek words polys, meaning "many", and thrix, meaning "hair". This name was used in ancient times to refer to plants with fine, hairlike parts, including mosses, but this application specifically refers to the hairy calyptras found on young sporophytes. A similar naming related to hair appears in Old Norse, haddr silfjar, "hair of Sif", goddess from Norse Mythology, wife of the god Thor. There are two major sections of Polytrichum species. The first — section Polytrichum — has narrow, toothed, and relatively erect leaf margins. The other — section Juniperifolia — has broad, entire, and sharply inflexed leaf margins that enclose the lamellae on the upper leaf surface. Polytrichum reproduce by vegetative and sexual methods.

Plant stem Structural axis of a vascular plant

A stem is one of two main structural axes of a vascular plant, the other being the root. It supports leaves, flowers and fruits, transports water and dissolved substances between the roots and the shoots in the xylem and phloem, stores nutrients, and produces new living tissue.

<i>Pogonatum urnigerum</i> Species of moss

Pogonatum urnigerum is a species of moss in the family Polytrichaceae, commonly called urn haircap. The name comes from "urna" meaning "urn" and "gerere" meaning "to bear" which is believed to be a reference made towards the plant's wide-mouthed capsule. It can be found on gravelly banks or similar habitats and can be identified by the blue tinge to the overall green colour. The stem of this moss is wine red and it has rhizoids that keep the moss anchored to substrates. It is an acrocarpous moss that grows vertically with an archegonium borne at the top of each fertilized female gametophyte shoot which develops an erect sporophyte.

References

  1. 1 2 B.O. van Zanten (2012). "Australian Mosses Online" (PDF). pp. 48. Polytrichaceae: Dawsonia.
  2. 1 2 Taranaki Educational Resource: Research, Analysis and Information Network. "Dawsonia" . Retrieved 7 February 2013.
  3. Encyclopedia of Life. "Details for: Dawsonia longifolia". Encyclopedia of Life . Retrieved 2013-07-23.
  4. "Dawsonia longifolia". The New York Botanical Garden. Retrieved 2013-07-23.
  5. "Dawsonia longifolia". Tropicos. Retrieved 2013-07-23.
  • Glime, Janice M. (2007). "Water relations: Conducting structures". Physiological Ecology. Bryophyte Ecology. Vol. 1. Michigan Technological University and International Association of Bryologists. Retrieved 9 March 2009.
  • Hébant, Charles (1 December 1974). "Polarized accumulations of endoplasmic reticulum and other ultrastructural features of leptoids in Polytrichadelphus magellanicus gametophytes". Protoplasma. 81 (4): 373–382. doi:10.1007/BF01281050. S2CID   40556117.