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Vittarioideae

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59-413: See text . Adiantoideae (C.Presl) R.M.Tryon Vittarioideae is a subfamily of the fern family Pteridaceae , in the order Polypodiales . The subfamily includes the previous families Adiantaceae (adiantoids or maidenhair ferns) and Vittariaceae (vittarioids or shoestring ferns). The subfamily includes two distinct groups of ferns: the adiantoids, consisting of the single genus Adiantum , and

118-479: A "single common ancestor" organism. Paraphyly is common in speciation , whereby a mother species (a paraspecies ) gives rise to a daughter species without itself becoming extinct. Research indicates as many as 20 percent of all animal species and between 20 and 50 percent of plant species are paraphyletic. Accounting for these facts, some taxonomists argue that paraphyly is a trait of nature that should be acknowledged at higher taxonomic levels. Cladists advocate

177-592: A cell nucleus, a plesiomorphy ) from its excluded descendants. Also, some systematists recognize paraphyletic groups as being involved in evolutionary transitions, the development of the first tetrapods from their ancestors for example. Any name given to these hypothetical ancestors to distinguish them from tetrapods—"fish", for example—necessarily picks out a paraphyletic group, because the descendant tetrapods are not included. Other systematists consider reification of paraphyletic groups to obscure inferred patterns of evolutionary history. The term " evolutionary grade "

236-734: A class Equisetopsida ( Embryophyta ) encompassing all land plants. This is referred to as Equisetopsida sensu lato to distinguish it from the narrower use to refer to horsetails alone, Equisetopsida sensu stricto . They placed the lycopods into subclass Lycopodiidae and the ferns, keeping the term monilophytes, into five subclasses, Equisetidae, Ophioglossidae, Psilotidae, Marattiidae and Polypodiidae, by dividing Smith's Psilotopsida into its two orders and elevating them to subclass (Ophioglossidae and Psilotidae). Christenhusz et al. (2011) followed this use of subclasses but recombined Smith's Psilotopsida as Ophioglossidae, giving four subclasses of ferns again. Christenhusz and Chase (2014) developed

295-415: A false indusium formed from the reflexed leaf margin. The family also includes a species, Vittaria appalachiana , that is highly unusual in that the sporophyte stage of the life cycle is absent. This species consists solely of photosynthetic gametophytes that reproduce asexually. Molecular phylogenetic analysis demonstrated that the vittarioid ferns were nested within the genus Adiantum as it

354-634: A few species (e.g., Cyathea brownii on Norfolk Island and Cyathea medullaris in New Zealand ). Roots are underground non-photosynthetic structures that take up water and nutrients from soil . They are always fibrous and are structurally very similar to the roots of seed plants. As in all vascular plants , the sporophyte is the dominant phase or generation in the life cycle . The gametophytes of ferns, however, are very different from those of seed plants. They are free-living and resemble liverworts , whereas those of seed plants develop within

413-405: A group of vascular plants (plants with xylem and phloem ) 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. Ferns have complex leaves called megaphylls that are more complex than

472-419: A group of dinosaurs (part of Diapsida ), both of which are "reptiles". Osteichthyes , bony fish, are paraphyletic when circumscribed to include only Actinopterygii (ray-finned fish) and Sarcopterygii (lungfish, etc.), and to exclude tetrapods ; more recently, Osteichthyes is treated as a clade, including the tetrapods. The " wasps " are paraphyletic, consisting of the narrow-waisted Apocrita without

531-439: A kind of lizard). Put another way, viviparity is a synapomorphy for Theria within mammals, and an autapomorphy for Eulamprus tympanum (or perhaps a synapomorphy, if other Eulamprus species are also viviparous). Groupings based on independently-developed traits such as these examples of viviparity represent examples of polyphyly , not paraphyly. The following list recapitulates a number of paraphyletic groups proposed in

590-560: A more inclusive clade, it often makes sense to study the paraphyletic group that remains without considering the larger clade. For example, the Neogene evolution of the Artiodactyla (even-toed ungulates, like deer, cows, pigs and hippopotamuses - Cervidae , Bovidae , Suidae and Hippopotamidae , the families that contain these various artiodactyls, are all monophyletic groups) has taken place in environments so different from that of

649-487: A new classification of ferns and lycopods. They used the term Polypodiophyta for the ferns, subdivided like Smith et al. into four groups (shown with equivalents in the Smith system), with 21 families, approximately 212 genera and 10,535 species; This was a considerable reduction in the number of families from the 37 in the system of Smith et al., since the approach was more that of lumping rather than splitting. For instance

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708-872: A number of families were reduced to subfamilies. Subsequently, a consensus group was formed, the Pteridophyte Phylogeny Group (PPG), analogous to the Angiosperm Phylogeny Group , publishing their first complete classification in November 2016. They recognise ferns as a class, the Polypodiopsida, with four subclasses as described by Christenhusz and Chase, and which are phylogenetically related as in this cladogram: Equisetales Ophioglossales Psilotales Marattiales Osmundales Hymenophyllales Gleicheniales Schizaeales Paraphyly Paraphyly

767-424: A phylogenetic species concept that does not consider species to exhibit the properties of monophyly or paraphyly, concepts under that perspective which apply only to groups of species. They consider Zander's extension of the "paraphyletic species" argument to higher taxa to represent a category error When the appearance of significant traits has led a subclade on an evolutionary path very divergent from that of

826-462: A protective coating called an indusium . The arrangement of the sporangia is important in classification. In monomorphic ferns, the fertile and sterile leaves look morphologically the same, and both are able to photosynthesize. In hemidimorphic ferns, just a portion of the fertile leaf is different from the sterile leaves. In dimorphic (holomorphic) ferns, the two types of leaves are morphologically distinct . The fertile leaves are much narrower than

885-430: A short-lived structure anchored to the ground by rhizoids called gametophyte which produce gametes. When a mature fertile frond bears sori, and spores are released, the spores will settle on the soil and send out rhizoids , while it develops into a prothallus . The prothallus bears spherical antheridia ( s.g. antheridium ) which produce antherozoids (male gametophytes) and archegonia ( s.g. archegonium ) which release

944-568: A single oosphere . The antherozoid swims up the archegonium and fertilize the oosphere, resulting in a zygote, which will grow into a separate sporophyte, while the gametophyte shortly persists as a free-living plant. Carl Linnaeus (1753) originally recognized 15 genera of ferns and fern allies, classifying them in class Cryptogamia in two groups, Filices (e.g. Polypodium ) and Musci (mosses). By 1806 this had increased to 38 genera, and has progressively increased since ( see Schuettpelz et al (2018) ). Ferns were traditionally classified in

1003-525: Is embedded in Haplopteris ; the segregation of Vaginularia from Monogramma was also supported, as members of Vaginularia formed a clade sister to Rheopteris and distant from Monogramma sensu stricto . A later molecular phylogeny, published in 2016, established the genus Antrophyopsis (formerly a subgenus of Antrophyum ) for three species placed in Scoliosorus but more distant from

1062-500: Is polyphyletic , the term fern allies should be abandoned, except in a historical context. More recent genetic studies demonstrated that the Lycopodiophyta are more distantly related to other vascular plants , having radiated evolutionarily at the base of the vascular plant clade , while both the whisk ferns and horsetails are as closely related to leptosporangiate ferns as the ophioglossoid ferns and Marattiaceae . In fact,

1121-419: Is a taxonomic term describing a grouping that consists of the grouping's last common ancestor and some but not all of its descendant lineages. The grouping is said to be paraphyletic with respect to the excluded subgroups. In contrast, a monophyletic grouping (a clade ) includes a common ancestor and all of its descendants. The terms are commonly used in phylogenetics (a subfield of biology ) and in

1180-439: Is a monophyletic group from which one or more subsidiary clades (monophyletic groups) are excluded to form a separate group. Philosopher of science Marc Ereshefsky has argued that paraphyletic taxa are the result of anagenesis in the excluded group or groups. A cladistic approach normally does not grant paraphyletic assemblages the status of "groups", nor does it reify them with explanations, as in cladistics they are not seen as

1239-433: Is allowed as a synonym of Magnoliopsida. Phylogenetic analysis indicates that the monocots are a development from a dicot ancestor. Excluding monocots from the dicots makes the latter a paraphyletic group. Among animals, several familiar groups are not, in fact, clades. The order Artiodactyla ( even-toed ungulates ) as traditionally defined is paraphyletic because it excludes Cetaceans (whales, dolphins, etc.). Under

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1298-578: Is intermediate between the eusporangiate ferns and the leptosporangiate ferns. Rai and Graham (2010) broadly supported the primary groups, but queried their relationships, concluding that "at present perhaps the best that can be said about all relationships among the major lineages of monilophytes in current studies is that we do not understand them very well". Grewe et al. (2013) confirmed the inclusion of horsetails within ferns sensu lato , but also suggested that uncertainties remained in their precise placement. Other classifications have raised Ophioglossales to

1357-442: Is paraphyletic with respect to birds . Reptilia contains the last common ancestor of reptiles and all descendants of that ancestor except for birds. Other commonly recognized paraphyletic groups include fish , monkeys , and lizards . The term paraphyly , or paraphyletic , derives from the two Ancient Greek words παρά ( pará ), meaning "beside, near", and φῦλον ( phûlon ), meaning "genus, species", and refers to

1416-613: Is present, it is found in the stem. Their foliage may be deciduous or evergreen , and some are semi-evergreen depending on the climate. Like the sporophytes of seed plants, those of ferns consist of stems, leaves and roots. Ferns differ from spermatophytes in that they reproduce by spores rather than having flowers and producing seeds. However, they also differ from spore-producing bryophytes in that, like seed plants, they are polysporangiophytes , their sporophytes branching and producing many sporangia. Also unlike bryophytes, fern sporophytes are free-living and only briefly dependent on

1475-482: Is sometimes used for paraphyletic groups. Moreover, the concepts of monophyly , paraphyly, and polyphyly have been used in deducing key genes for barcoding of diverse group of species. Current phylogenetic hypotheses of tetrapod relationships imply that viviparity , the production of offspring without the external laying of a fertilized egg, developed independently in the lineages that led to humans ( Homo sapiens ) and southern water skinks ( Eulampus tympanum ,

1534-514: The Cetacea (whales, dolphins, and porpoises) that the Artiodactyla are often studied in isolation even though the cetaceans are a descendant group. The prokaryote group is another example; it is paraphyletic because it is composed of two Domains (Eubacteria and Archaea) and excludes (the eukaryotes ). It is very useful because it has a clearly defined and significant distinction (absence of

1593-581: The ICN ) abandoned consideration of bacterial nomenclature in 1975; currently, prokaryotic nomenclature is regulated under the ICNB with a starting date of 1 January 1980 (in contrast to a 1753 start date under the ICBN/ICN). Among plants, dicotyledons (in the traditional sense) are paraphyletic because the group excludes monocotyledons . "Dicotyledon" has not been used as a botanic classification for decades, but

1652-660: The ants and bees . The sawflies ( Symphyta ) are similarly paraphyletic, forming all of the Hymenoptera except for the Apocrita, a clade deep within the sawfly tree. Crustaceans are not a clade because the Hexapoda (insects) are excluded. The modern clade that spans all of them is the Tetraconata . One of the goals of modern taxonomy over the past fifty years has been to eliminate paraphyletic "groups", such as

1711-479: The class Filices, and later in a Division of the Plant Kingdom named Pteridophyta or Filicophyta. Pteridophyta is no longer recognised as a valid taxon because it is paraphyletic . The ferns are also referred to as Polypodiophyta or, when treated as a subdivision of Tracheophyta (vascular plants), Polypodiopsida, although this name sometimes only refers to leptosporangiate ferns. Traditionally, all of

1770-566: The microphylls of clubmosses . Most ferns are leptosporangiate ferns . They produce coiled fiddleheads that uncoil and expand into fronds . The group includes about 10,560 known extant species. Ferns are defined here in the broad sense, being all of the Polypodiopsida , comprising both the leptosporangiate ( Polypodiidae ) and eusporangiate ferns , the latter group including horsetails , whisk ferns , marattioid ferns , and ophioglossoid ferns . The fern crown group , consisting of

1829-448: The tree model of historical linguistics . Paraphyletic groups are identified by a combination of synapomorphies and symplesiomorphies . If many subgroups are missing from the named group, it is said to be polyparaphyletic. The term received currency during the debates of the 1960s and 1970s accompanying the rise of cladistics , having been coined by zoologist Willi Hennig to apply to well-known taxa like Reptilia ( reptiles ), which

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1888-584: The Pteridophyte Phylogeny Group classification of 2016 (PPG I): The following phylogeny for the currently recognized genera of the subfamily was presented by Schuettpelz et al. : Adiantum Rheopteris Vaginularia Hecistopteris Radiovittaria Haplopteris (including Monogramma s.s.) Antrophyopsis Antrophyum Polytaenium Scoliosorus Ananthacorus Vittaria Fern The ferns ( Polypodiopsida or Polypodiophyta ) are

1947-495: The actual products of evolutionary events. A group whose identifying features evolved convergently in two or more lineages is polyphyletic (Greek πολύς [ polys ], "many"). More broadly, any taxon that is not paraphyletic or monophyletic can be called polyphyletic. Empirically, the distinction between polyphyletic groups and paraphyletic groups is rather arbitrary, since the character states of common ancestors are inferences, not observations. These terms were developed during

2006-490: The debates of the 1960s and 1970s accompanying the rise of cladistics . Paraphyletic groupings are considered problematic by many taxonomists, as it is not possible to talk precisely about their phylogenetic relationships, their characteristic traits and literal extinction. Related terms are stem group , chronospecies , budding cladogenesis, anagenesis, or 'grade' groupings. Paraphyletic groups are often relics from outdated hypotheses of phylogenic relationships from before

2065-478: The descendants of a unique common ancestor. By comparison, the term polyphyly , or polyphyletic , uses the Ancient Greek prefix πολύς ( polús ), meaning "many, a lot of", and refers to the fact that a polyphyletic group includes organisms arising from multiple ancestral sources. Groups that include all the descendants of a common ancestor are said to be monophyletic . A paraphyletic group

2124-450: The examples given here, from formal classifications. Species have a special status in systematics as being an observable feature of nature itself and as the basic unit of classification. Some articulations of the phylogenetic species concept require species to be monophyletic, but paraphyletic species are common in nature, to the extent that they do not have a single common ancestor. Indeed, for sexually reproducing taxa, no species has

2183-431: The fronds are branched more than once, it can also be a combination of the pinnatifid are pinnate shapes. If the leaf blades are divided twice, the plant has bipinnate fronds, and tripinnate fronds if they branch three times, and all the way to tetra- and pentapinnate fronds. In tree ferns, the main stalk that connects the leaf to the stem (known as the stipe), often has multiple leaflets. The leafy structures that grow from

2242-494: The inclusion of Equisetaceae in the ferns, notably relating to the construction of their sperm and peculiarities of their roots. The leptosporangiate ferns are sometimes called "true ferns". This group includes most plants familiarly known as ferns. Modern research supports older ideas based on morphology that the Osmundaceae diverged early in the evolutionary history of the leptosporangiate ferns; in certain ways this family

2301-474: The leptosporangiate ferns. The Marattiaceae are a primitive group of tropical ferns with large, fleshy rhizomes and are now thought to be a sibling taxon to the leptosporangiate ferns. Several other groups of species were considered fern allies: the clubmosses , spikemosses , and quillworts in Lycopodiophyta ; the whisk ferns of Psilotaceae ; and the horsetails of Equisetaceae . Since this grouping

2360-585: The leptosporangiates and eusporangiates, is estimated to have originated in the late Silurian period 423.2 million years ago, but Polypodiales , the group that makes up 80% of living fern diversity, did not appear and diversify until the Cretaceous , contemporaneous with the rise of flowering plants that came to dominate the world's flora. Ferns are not of major economic importance, but some are used for food, medicine, as biofertilizer , as ornamental plants, and for remediating contaminated soil. They have been

2419-622: The literature, and provides the corresponding monophyletic taxa. The concept of paraphyly has also been applied to historical linguistics , where the methods of cladistics have found some utility in comparing languages. For instance, the Formosan languages form a paraphyletic group of the Austronesian languages because they consist of the nine branches of the Austronesian family that are not Malayo-Polynesian and are restricted to

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2478-555: The maternal gametophyte . The green , photosynthetic part of the plant is technically a megaphyll and in ferns, it is often called a frond . New leaves typically expand by the unrolling of a tight spiral called a crozier or fiddlehead into fronds . This uncurling of the leaf is termed circinate vernation . Leaves are divided into two types: sporophylls and tropophylls. Sporophylls produce spores; tropophylls do not. Fern spores are borne in sporangia which are usually clustered to form sori . The sporangia may be covered with

2537-461: The name "Vittarioideae" in Verdoorn 's Manual of Pteridology in 1938, but did not include a description, leaving it nomenclaturally invalid. Ren-Chang Ching raised Vittariaceae to the rank of a family in 1940. The first well-sampled molecular phylogenetic study of the vittarioids was based on the chloroplast gene rbcL . In this study, it was found that the type species of Monogramma

2596-430: The rank of a fifth class, separating the whisk ferns and ophioglossoid ferns. The ferns are related to other groups as shown in the following cladogram: Lycophytes [REDACTED] Ferns [REDACTED] Gymnosperms [REDACTED] Angiosperms [REDACTED] The classification of Smith et al. in 2006 treated ferns as four classes: In addition they defined 11 orders and 37 families. That system

2655-696: The ranks of the ICZN Code , the two taxa are separate orders. Molecular studies, however, have shown that the Cetacea descend from artiodactyl ancestors, although the precise phylogeny within the order remains uncertain. Without the Cetaceans the Artiodactyls are paraphyletic. The class Reptilia is paraphyletic because it excludes birds (class Aves ). Under a traditional classification, these two taxa are separate classes. However birds are sister taxon to

2714-567: The rise of cladistics. The prokaryotes (single-celled life forms without cell nuclei) are a paraphyletic grouping, because they exclude the eukaryotes , a descendant group. Bacteria and Archaea are prokaryotes, but archaea and eukaryotes share a common ancestor that is not ancestral to the bacteria. The prokaryote/eukaryote distinction was proposed by Edouard Chatton in 1937 and was generally accepted after being adopted by Roger Stanier and C.B. van Niel in 1962. The botanical code (the ICBN, now

2773-405: The situation in which one or several monophyletic subgroups of organisms (e.g., genera, species) are left apart from all other descendants of a unique common ancestor. Conversely, the term monophyly , or monophyletic , builds on the Ancient Greek prefix μόνος ( mónos ), meaning "alone, only, unique", and refers to the fact that a monophyletic group includes organisms consisting of all

2832-476: The spore producing vascular plants were informally denominated the pteridophytes , rendering the term synonymous with ferns and fern allies . This can be confusing because members of the division Pteridophyta were also denominated pteridophytes ( sensu stricto ). Traditionally, three discrete groups have been denominated ferns: two groups of eusporangiate ferns, the families Ophioglossaceae ( adder's tongues , moonworts , and grape ferns) and Marattiaceae ; and

2891-417: The spore wall and are dependent on the parent sporophyte for their nutrition. A fern gametophyte typically consists of: The lifecycle of a fern involves two stages, as in club mosses and horsetails . In stage one, the spores are produced by sporophytes in sporangia , which are clustered together in sori ( s.g. sorus ), developing on the underside of fertile fronds. In stage two, the spores germinate into

2950-496: The sterile leaves, and may have no green tissue at all, as in the Blechnaceae and Lomariopsidaceae . The anatomy of fern leaves can be anywhere from simple to highly divided, or even indeterminate (e.g. Gleicheniaceae , Lygodiaceae ). The divided forms are pinnate , where the leaf segments are completely separated from one other, or pinnatifid (partially pinnate), where the leaf segments are still partially connected. When

3009-463: The stipe are known as pinnae and are often again divided into smaller pinnules. Fern stems are often loosely called rhizomes , even though they grow underground only in some of the species. Epiphytic species and many of the terrestrial ones have above-ground creeping stolons (e.g., Polypodiaceae ), and many groups have above-ground erect semi-woody trunks (e.g., Cyatheaceae , the scaly tree ferns). These can reach up to 20 meters (66 ft) tall in

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3068-498: The subject of research for their ability to remove some chemical pollutants from the atmosphere. Some fern species, such as bracken ( Pteridium aquilinum ) and water fern ( Azolla filiculoides ), are significant weeds worldwide. Some fern genera, such as Azolla , can fix nitrogen and make a significant input to the nitrogen nutrition of rice paddies . They also play certain roles in folklore. Extant ferns are herbaceous perennials and most lack woody growth. When woody growth

3127-585: The tribe, Ralph Benedict adopted a circumscription similar to modern treatments, within which he recognized the genera Ananthacorus , Anetium , Antrophyum , Hecistopteris , Monogramma , Polytaenium , and Vittaria . He described Radiovittaria as a subgenus of Vittaria , subsumed Scoliosorus within Polytaenium as doubtfully worthy of subgeneric rank, while Rheopteris had not yet been discovered. Haplopteris he explicitly synonymized with Vittaria in 1914. Carl Christensen used

3186-403: The type of that genus than Antrophyum . This treatment also sank Anetium into Polytaenium and Monogramma into Haplopteris . Since the name Monogramma has taxonomic priority over Haplopteris , a proposal to reject Monogramma in favor of Haplopteris has been put forth to conserve the name and comparatively stable circumscription of Haplopteris . The following genera are recognized in

3245-428: The vittarioids, several genera, including Vittaria , which typically have highly reduced leaves, usually entire, and an epiphytic habit. The ferns historically considered as Adiantum include both petrophilic and terrestrial plants. The vittarioid ferns are primarily epiphytic in tropical regions and all have simple leaves with sori that follow the veins and lack true indusia ; the sori are most often marginal with

3304-477: The whisk ferns and ophioglossoid ferns are demonstrably a clade , and the horsetails and Marattiaceae are arguably another clade. Smith et al. (2006) carried out the first higher-level pteridophyte classification published in the molecular phylogenetic era, and considered the ferns as monilophytes, as follows: Molecular data, which remain poorly constrained for many parts of the plants' phylogeny, have been supplemented by morphological observations supporting

3363-844: Was a consensus of a number of studies, and was further refined. The phylogenetic relationships are shown in the following cladogram (to the level of orders). This division into four major clades was then confirmed using morphology alone. Lycopodiophytes (club mosses, spike mosses, quillworts) Spermatophytes (seed plants) Equisetales (horsetails) [REDACTED] Ophioglossales (grapeferns etc.) Psilotales (whisk ferns) [REDACTED] Marattiales [REDACTED] Osmundales [REDACTED] Hymenophyllales (filmy ferns) [REDACTED] Gleicheniales [REDACTED] Schizaeales Salviniales (heterosporous) Cyatheales (tree ferns) [REDACTED] Polypodiales [REDACTED] Subsequently, Chase and Reveal considered both lycopods and ferns as subclasses of

3422-435: Was made by Carl Borivoj Presl in 1836, who erected the tribe Vittariaceae to contain the genera Vittaria and Prosaptia , the latter now included in the grammitid ferns. He invented the new genus Haplopteris to accommodate another group of simple-leaved ferns separated from Pteris , but placed it in tribe Adiantaceae instead, due to the location of its sori just behind the leaf margin. In his 1911 treatment of

3481-660: Was originally circumscribed , making that genus paraphyletic. In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the family is treated as the subfamily Vittarioideae] of the family Pteridaceae . The following diagram shows a likely phylogenetic relationship between the Vittarioideae and other subfamilies of the Pteridaceae. Cryptogrammoideae Parkerioideae (syn. Ceratopteridoideae) Pteridoideae Cheilanthoideae Vittarioideae The first suprageneric classification based on Vittaria

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