Polyphlebium venosum | |
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Scientific classification | |
Kingdom: | Plantae |
Clade: | Tracheophytes |
Division: | Polypodiophyta |
Class: | Polypodiopsida |
Order: | Hymenophyllales |
Family: | Hymenophyllaceae |
Genus: | Polyphlebium |
Species: | P. venosum |
Binomial name | |
Polyphlebium venosum (R.Br.) Copel. | |
Synonyms [1] | |
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Polyphlebium venosum, the veined bristle-fern or bristle filmy fern, is a fern in the family Hymenophyllaceae. It is only found in wet forests, mainly growing as an epiphyte on the shady side of the soft tree fern, Dicksonia antartica. [2] It also grows on logs, trunks of trees and rarely on trunks of Cyathea species or on wet rock-faces. It is found in the wetter parts of Eastern Australia and New Zealand. [3] P. venosum has poor long-distance dispersal compared to other ferns due to its short lived spore. Notable features of Polyphlebium venosum include it being one cell layer thick, 5–15 cm in length, having many branching veins and a trumpet shaped indusium.
The sporophyte stage has rhizome branched and creeping, very fine, densely covered with tiny, pale brown hairs. Fronds well spaced, pendent, 5–15 cm long, delicate and translucent; stipe and rachis thread-like. Lamina pale green, long and narrow, irregular in outline and simply lobed to pinnately divided; pinnae sometimes very long and hanging almost parallel to main rachis, lower pinnae often very small and widely spaced. Margins of pinnae or segments wavy or broadly crenate; ultimate segments blunt and broad (2–6 mm); veins prominent and repeatedly forked. Sori marginal and immersed, borne singly on short lateral lobes near base of pinna; indusium narrowly trumpet-shaped, 2–4 mm long; fine receptacle projecting 10 mm or more. [2]
The gametophyte is a branching uniseriate filament and bears numerous, small, stalked antheridia, each with a simple wall and an operculum which is raised or shed to allow the spermatozoids to escape. The archegonia, with straight necks and tiers of four to six neck cells, are borne on special structures, the archegoniophores. [4]
The species was first described by Robert Brown in 1810, as Trichomanes venosum. [5] The precise circumscription of the genus Trichomanes varies considerably between sources. As of October 2019 [update] , the Checklist of Ferns and Lycophytes of the World followed the Pteridophyte Phylogeny Group classification of 2016 (PPG I) in using a narrow circumscription of Trichomanes, [6] and placed this species in Polyphlebium as P. venosum. [1] It has also been placed in the genus Crepidomanes (another of the eight genera into which Trichomanes is divided in PPG I) as Crepidomanes venosum. [1] On the other hand, as of October 2019 [update] , Plants of the World Online used a broad circumscription of Trichomanes, so retaining Brown's original name. [7]
Due to Polyphlebium venosum being only one cell layer thick, it is heavily prone to desiccation in hot or dry environments. This is one of the main reasons that it grows as a mat on the shaded side of Dicksonia antartica .
P. venosum is at no threat of worldwide extinction, but extreme events like large-scale wildfires can reduce population sizes and exacerbate the effect of anthropogenic disturbances. Due to its heavy reliance on D. antartica the species has a limited dispersion rate which can be halted by dry landscapes acting as geological boundaries. [8] Like other ferns, P. venosum undergoes alteration of generations which consists of two sexual stages - the diploid sporophyte and the haploid gametophyte. The sporophyte stage of P. venosum consists of adult ferns which release numerous spores. These spores then settle on the trunks of D. antartica in a moist and sheltered habitat. Spores germinate within a few days and form a one cell layer thick, 'heart-shaped' prothallus. In ferns, the time required for the prothallus to sexually mature may require several months to several years of development. The male antheridia matures and releases its gametes earlier than the female archegonia in an effort to avoid self-fertilisation. [8] The prothallus can reproduce asexually through the release of gemmae which on germination produce rhizoids, filaments and antheridia or more gemmae. The prothallus can also reproduce itself vegetatively by regeneration. [4] Once established, P. venosum spreads to surrounding substrate through its extensively creeping rhizomes.
Spores of P. venosum take two days to germinate after sowing and are on average only viable for 48 days. After two weeks, only 1/10 billion of the original spores survive. Distribution of the spores places 90% in the immediate vicinity of the parent sporophyte. The short lived nature of P. venosum's spores compared to other ferns reduces their likelihood for long-distance dispersal. [8]
Polyphlebium venosum is only found in wet forests in Australia and New Zealand. In Australia, the distribution is restricted to the Eastern states of Tasmania, Victoria, New South Wales and Queensland. [2]
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.
The ferns are a group of vascular plants that reproduce via spores and have neither seeds nor flowers. They differ from mosses by being vascular, i.e., having specialized tissues that conduct water and nutrients and in having life cycles in which the branched sporophyte is the dominant phase.
Alternation of generations is the predominant type of life cycle in plants and algae. In plants both phases are multicellular: the haploid sexual phase – the gametophyte – alternates with a diploid asexual phase – the sporophyte.
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'.
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.
A pteridophyte is a vascular plant that disperses spores. Because pteridophytes produce neither flowers nor seeds, they are sometimes referred to as "cryptogams", meaning that their means of reproduction is hidden.
Marchantia is a genus of liverworts in the family Marchantiaceae and the order Marchantiales.
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.
The Hymenophyllaceae, the filmy ferns and bristle ferns, are a family of two to nine genera and about 650 known species of ferns, with a subcosmopolitan distribution, but generally restricted to very damp places or to locations where they are wetted by spray from waterfalls or springs. A recent fossil find shows that ferns of Hymenophyllaceae have existed since at least the Upper Triassic.
Trichomanes is a genus of ferns in the family Hymenophyllaceae, termed bristle ferns. The circumscription of the genus is disputed. All ferns in the genus are filmy ferns, with leaf tissue typically 2 cells thick. This thinness generally necessitates a permanently humid habitat, and makes the fronds somewhat translucent. Because of this membrane-like frond tissue, the plant is prone to drying out. “Filmy ferns” in the taxa Hymenophyllaceae grow in constantly wet environments. Many are found in cloud forests such as “Choco” in Colombia. There are also members of the taxa that can grow submersed in water.
Lophosoria quadripinnata(J.F.Gmel.) C.Chr. is a species of fern that, according to DNA molecular analysis, belongs to the family Dicksoniaceae, where it is placed in the genus Lophosoria. It is found in the Americas spanning from Cuba and Mexico to Chile. In Chile it is present in the area between Talca and Aysén including Juan Fernández Islands. In Argentina it grows only in the humid valleys of western Neuquén and Río Negro Province. Diamondleaf fern is a common name. In Spanish it is known as 'ampe' or palmilla, but one has to remember that there are several species of ferns called "palmillas" that have larger or smaller fronds, and which grow in colder climates. It is a medium-sized plant, growing to about 4–5 feet and even though the rhizome does not grow a trunk, it is clearly related to the other tree ferns due to features that were apparently already present in their common ancestor, like 'pneumathodes', and the rhizome which changed from the dorsiventral symmetry typical of the other ferns, to a radial symmetry typical of tree ferns. Their large and multiple pinnate fronds, with the petiole raised adaxially, and the hairs on the rhizome and lower part of the petioles, also resemble those of tree ferns. To identify the species, use the position and characteristics of the spores found on the fertile fronds. The genus already existed in the Cretaceous Period in southern Gondwana according to fossil remains found in Antarctica. The species is well known as an ornamental plant.
Crepidomanes intricatum, synonym Trichomanes intricatum, is known as the weft fern. The genus Crepidomanes is accepted in the Pteridophyte Phylogeny Group classification of 2016, but not by some other sources. As of October 2019, Plants of the World Online sank the genus into a broadly defined Trichomanes, treating this species as Trichomanes intricatum.
Diplazium australe, commonly known as the Austral lady fern, is a small fern occurring in eastern Australia, New Zealand and Norfolk Island. The habitat is moist shaded areas, often occurring in rainforest.
Hymenophyllum australe, commonly known as austral filmy fern, is a relatively large rupestral and epiphytic fern, indigenous to eastern Australia and New Zealand. It belongs to the unique Hymenophyllum genus, which are characterised by their thin membranous fronds that are seldom more than one cell thick, with the exception of regions over and around veins. Hymenophyllum australe is distinctive in that the fronds are typically thicker than other Hymenophyllum species, often being up to 2-3 cells thick.
Hymenophyllum flabellatum, the shiny filmy-fern, is a species of fern in the family Hymenophyllaceae. This delicate fern is commonly epiphytic and is between 5 and 25 cm in length. It is distinct, with its thin, one-celled thick, membranous leaves. It is from the family Hymenophyllaceae and is dispersed world wide. The species is dispersed highly throughout Tasmanian rainforests and in the south east of mainland Australia, with small pockets of the population seen in northern Queensland.
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.
Vandenboschia boschiana, synonym Trichomanes boschianum, also known as the Appalachian bristle fern or Appalachian filmy fern, is a small delicate perennial leptosporangiate fern which forms colonies with long, black creeping rhizomes.
Hymenophyllum tunbrigense, the Tunbridge filmy fern or Tunbridge filmy-fern, is a small, fragile perennial leptosporangiate fern which forms large dense colonies of overlapping leaves from creeping rhizomes. The common name derives from the leaves which are very thin, only a single cell thick, and translucent, giving the appearance of a wet film. The evergreen fronds are bipinnatifid, deeply and irregularly dissected, about 3 to 6 cm long, 2 cm across with dark winged stipes. In contrast to the similar H. wilsonii the fronds are more divided, flattened, appressed to the substrate and tend to have a bluish tint.
Syntrichia latifolia, formerly Tortula latifolia, and commonly known as water screw-moss, is a species of moss belonging to the family Pottiaceae. Syntrichia species differ from members of Tortula due to synapomorphic leaf qualities, such as different basal and distal cells, as well as different costal cross sections where Tortula has an abaxial epidermis and Syntrichia lacks one.
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