Lophosoria quadripinnata

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Lophosoria quadripinnata
Lophosoria quadripinnata-fronda.JPG
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Division: Polypodiophyta
Class: Polypodiopsida
Order: Cyatheales
Family: Dicksoniaceae
Genus: Lophosoria
Species:
L. quadripinnata
Binomial name
Lophosoria quadripinnata
Synonyms [1]
  • Alsophila affinis(C.Presl) Fée
  • Alsophila bilineataSodiro
  • Alsophila christiiSodiro
  • Alsophila deckerianaKlotzsch
  • Alsophila glauca(Sw.) Urb.
  • Alsophila millefoliumDesv.
  • Alsophila monticolaMart.
  • Alsophila pruinata(Sw.) Kaulf.
  • Alsophila quadripinnata(J.F.Gmel.) C.Chr.
  • Alsophila schaffnerianaFée
  • Cyathea bilineata(Sodiro) Domin
  • Cyathea discolorBory
  • Cyathea monticolaC.Presl
  • Cyathea quadripinnata(J.F.Gmel.) Domin
  • Cyathea schaffneriana(Fée) Domin
  • Lophosoria acaulisFée
  • Lophosoria affinisC.Presl
  • Lophosoria brasiliensisKlotzsch
  • Lophosoria caesiaFée
  • Lophosoria densa(Liebm.) Klotzsch
  • Lophosoria discolorC.Presl
  • Lophosoria excisaFée
  • Lophosoria frigida(Liebm.) Klotzsch\n
  • Lophosoria glaucaKuhn
  • Lophosoria glaucescens(Liebm.) Klotzsch
  • Lophosoria polypodioidesC.Presl
  • Lophosoria prostrataFée
  • Lophosoria pruinata(Sw.) C.Presl
  • Lophosoria schaffneriana(Fée) E.Fourn.
  • Lophosoria warscewicziiKlotzsch ex E.Fourn.
  • Polypodium caesiumC.Presl
  • Polypodium cinereum Cav.
  • Polypodium glaucumSw.
  • Polypodium griseumSchkuhr
  • Polypodium maculatumSpreng.
  • Polypodium pruinatumSw.
  • Polypodium quadripinnatumJ.F.Gmel.
  • Trichosorus densusLiebm.
  • Trichosorus frigidusLiebm.
  • Trichosorus glaucescensLiebm.

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. [2] In Spanish it is known as 'ampe' (from the Mapudungun añpe) 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 (though 10–12 feet in a sheltered place at Arduaine Garden in Argyll, Scotland) 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.

Contents

Habitat of Lophosoria quadripinnata Lophosoria quadripinnata.jpg
Habitat of Lophosoria quadripinnata

Description

Lophosoria quadripinnata is a vascular plant with two alternating generations, a sporophyte and a gametophyte, multicellular and independent; with spores as a means of dispersion and survival. The gametophyte is a "thallus" (undifferentiated tissue), and the sporophyte is a "corm" (with roots, shoots, and a vascular system). Due to these characteristics it is usually classified as a "pteridophyte". They have sporophytes with megaphylls or "fronds" (Euphyllophytina).

The rhizome is massive, with hairs, not growing a trunk (not arborescent), and with radial symmetry instead of horizontal; a characteristic apparently originating in the ancestor of the tree ferns. The fronds are large in size, 2-3 pinnations, with hairs on the under side of the petioles, and they are high on its abaxial part, all common characteristics of the Cyatheales order (the tree ferns clade). Also present are the pneumathodes (discrete vent lines, or patches, present on the rachis, petiole and rhizome, whose function is facilitating gas exchange in the dense tissue), which are characteristic of the tree fern clade.

Details of the adaxial face of the frond of Lophosoria quadripinnata Lophosoria quadripinnata-detalle.JPG
Details of the adaxial face of the frond of Lophosoria quadripinnata

The sori, without indusia (covering), are located on the abaxial (lower) surface, on the veins of the last pinnae. The leaf margin does not form part of an indusium, as in other Dicksoniaceae. The sori have numerous hairs (called "filiform paraphyses") between the sporangia. The characteristics and position of the sori are unique and can be used to identify the species.

Like all Polypodiopsidas, the sporangia are leptosporangiate (with a foot, capsule with a single-cell wall thickness, and dehiscent ring in the capsule). As in all the tree ferns, the ring is oblique and complete, not interrupted by the foot of the sporangium. The spores have trilete marks. This species has spores with a very unusual morphology, with a central belt ("cincture") that meant for a long time the species was assigned its own family, Lophosoriaceae.

The germination of the gametophyte corresponds to the genus Cyathea, giving rise to short strands of from two to six cells in both varieties. The prothallus development is of the Adiantum type. When raised in the laboratory, gametophytes of the quadripinnata variety are always chordates, however gametophytes of the contracta variety possess three morphs, depending on the density of spores that are developed (Dyer 1979 [3] ). At low density, they are long spatulates with a central meristem and a slightly more developed wing than the other; at medium densities they are cordiforms and at high densities are band-like with a large amount of antheridia.

The gametophyte is protandric (a hermaphrodite, first antheridia are developed that give antherozoids, and then the archegonia that gives the oospheres). The number of x chromosomes = 65.

Taxonomy

Theoretical introduction to Phylogenetics and Taxonomy

Genetic analysis has placed the species unequivocally in the family Dicksoniaceae, but the story of its taxonomic placement is long. Pichi Sermolli (1970 [4] ) placed it in its own family, Lophosoriaceae Pichi Sermolli, where it was located for a long time. At first it was thought to be a relation of the Cyatheaceae because of the characteristic abaxial sori, or the pattern of gametophyte germination. In the 1990s a close relationship was hypothesized with Metaxyaceae because of characteristics of the petiole and stem morphology but subsequent analyzes suggested that these families were not related (D. S. Conant, unpublished data, cited in Wolf et al. 1999 [5] ). On the other hand, ultrastructural studies (using scanning electron microscopy) of the spores (Gastony y Tyron 1976 [6] ) and recent studies of gametophyte development (Pérez-García et al. 1995 [7] ) have concluded that Lophosoria differs significantly from the characteristics of other tree ferns, so their relationship to the others remains unknown.

Other researchers, such as Kubitzki in Kramer (1990 [8] ) have it nested within Dicksoniaceae along with other genera that today are classified in other families of tree ferns. As molecular studies of the species continued, there was an increasingly obvious affinity with the family Dicksoniaceae, such as having the same number of chromosomes, and molecular DNA analysis done on rbcL sequence in 1999 also placed it within that family (Wolf et al. 1999 [5] ), a relationship that was confirmed in an extensive molecular study of ferns made by Korall et al. (2006, [9] on the sequences atpA, atpB, rps4 and the aforementioned). Because of that the species was placed in the family Dicksoniaceae in its own monotypic genus in Smith's 2006 classification system of monilophytes. [10]

Circumscription: the species consists of at least two varieties, sometimes placed as species of the genus:

The spores of the contracta variety are slightly bigger (70 x 75 μm) than those of the quadripinnata variety (50 × 60 μm). Furthermore, the quadripinnata variety's antheridia are made up of 5 cells: 2 baseline, 2 annular, and a small elliptical operculum, while those of the variety contracta are formed by three cells, one basal an annular and operculum (Stockey 1930 [11] ). They also differ in the morphology of their gametophytes.

Another variety Lophosoria quadripinnata variety quesadae A.Rojas has also been described in Costa Rica and Panama (Rojas-Alvarado 1996, it was described as Lophosoria quesadae species [12] ).

Evolution

Lophosoria apparently originated in the early Cretaceous Period, on the southern continent of Gondwana, and existed when the continent split in the late Cretaceous Period. Gondwana.jpg
Lophosoria apparently originated in the early Cretaceous Period, on the southern continent of Gondwana, and existed when the continent split in the late Cretaceous Period.

Dettmann (1986 [13] ) has remarked that the spores of the extinct genus Cyatheacidites correspond very well with living Lophosoria. The distribution of the Cyatheacidites has been used to infer that Lophosoria was located in the southern part of Gondwana during the Early Cretaceous Period, and then migrated to Australia and South America (Dettmann 1986 [13] ).

More recently, Cantrill (1998 [14] ) described fossilized leaves in the early Cretaceous layer (more specifically in the Aptian) in Antarctica, which contained spores of Cyatheacidites. The preservation of the leaves and spores was so good that Cantrill could identify the species, and described them by the name of Lophosoria cupulataD.J.Cantrill (published as Lophosoria cupulatus) with the genus change, as he considered Lophosoria quadripinnata(J.F.Gmel.) C.Chr. was the living species more closely related to the species found.

Economic importance

It is used as an ornamental plant in parks and gardens, as well as cut foliage in flower bouquets. [15] The plants used in latter are removed from their natural environment, creating certain local conservation issues. Some local markets in the south of Chile sell their sprouts, called perritos, for consuming in salads. [16]

Related Research Articles

<span class="mw-page-title-main">Tree fern</span> Ferns that grow with a trunk elevating the fronds above ground level

The tree ferns are arborescent (tree-like) ferns that grow with a trunk elevating the fronds above ground level, making them trees. Many extant tree ferns are members of the order Cyatheales, to which belong the families Cyatheaceae, Dicksoniaceae, Metaxyaceae, and Cibotiaceae. It is estimated that Cyatheales originated in the early Jurassic, and is the third group of ferns known to have given rise to tree-like forms. The others are the extinct Tempskya of uncertain position, and Osmundales where the extinct Guaireaceae and some members of Osmundaceae also grew into trees. In addition there were the Psaroniaceae and Tietea in the Marattiales, which is the sister group to most living ferns including Cyatheales.

<span class="mw-page-title-main">Alternation of generations</span> Reproductive cycle of plants and algae

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.

<span class="mw-page-title-main">Osmundaceae</span> Family of ferns

Osmundaceae is a family of ferns containing four to six extant genera and 18–25 known species. It is the only living family of the order Osmundales in the class Polypodiopsida (ferns) or in some classifications the only order in the class Osmundopsida. This is an ancient and fairly isolated group that is often known as the "flowering ferns" because of the striking aspect of the ripe sporangia in Claytosmunda, Osmunda, Osmundastrum, and Plensium. In these genera the sporangia are borne naked on non-laminar pinnules, while Todea and Leptopteris bear sporangia naked on laminar pinnules. Ferns in this family are larger than most other ferns.

<span class="mw-page-title-main">Cyatheales</span> Order of ferns

The order Cyatheales, which includes most tree ferns, is a taxonomic order of the fern class, Polypodiopsida. No clear morphological features characterize all of the Cyatheales, but DNA sequence data indicate the order is monophyletic. Some species in the Cyatheales have tree-like growth forms from a vertical rhizome, others have shorter or horizontal expanding rhizomes.

<span class="mw-page-title-main">Marsileaceae</span> Family of ferns

Marsileaceae is a small family of heterosporous aquatic and semi-aquatic ferns, though at first sight they do not physically resemble other ferns. The group is commonly known as the "pepperwort family" or as the "water-clover family" because the leaves of the genus Marsilea superficially resemble the leaves of a four-leaf clover. In all, the family contains 3 genera and 50 to 80 species with most of those belonging to Marsilea.

<i>Platycerium</i> Genus of ferns

Platycerium is a genus of about 18 fern species in the polypod family, Polypodiaceae. Ferns in this genus are widely known as staghorn or elkhorn ferns due to their uniquely shaped fronds. This genus is epiphytic and is native to tropical and temperate areas of South America, Africa, Southeast Asia, Australia, and New Guinea.

<span class="mw-page-title-main">Pteridophyte</span> Group of plants that reproduce by spores

A pteridophyte is a vascular plant that reproduces by means of spores. Because pteridophytes produce neither flowers nor seeds, they are sometimes referred to as "cryptogams", meaning that their means of reproduction is hidden.

<span class="mw-page-title-main">Cyatheaceae</span> Family of ferns

The Cyatheaceae are a family of ferns, the scaly tree ferns, one of eight families in the order Cyatheales in the Pteridophyte Phylogeny Group classification of 2016. Alternatively, the family may defined much more broadly as the only family in the Cyatheales, with the PPG I family treated as the subfamily Cyatheoideae. The narrower circumscription is used in this article.

<span class="mw-page-title-main">Dicksoniaceae</span> Family of ferns

Dicksoniaceae is a group of tropical, subtropical and warm temperate ferns, treated as a family in the Pteridophyte Phylogeny Group classification of 2016, and counting 30-40 species. Alternatively, the family may be sunk into a very broadly defined family Cyatheaceae sensu lato as the subfamily Dicksonioideae. Most of the genera in the family are terrestrial ferns or have very short trunks compared to tree ferns of the family Cyatheaceae sensu stricto. However, some of the larger species can reach several metres in height. A number of others are epiphytes. They are found mostly in tropical regions in the Southern Hemisphere, as far south as southern New Zealand. Larger tree ferns in the genus Cibotium were formerly included in Dicksoniaceae, but are now segregated as the family Cibotiaceae.

<i>Onoclea sensibilis</i> Species of fern

Onoclea sensibilis, the sensitive fern, also known as the bead fern, is a coarse-textured, medium to large-sized deciduous perennial fern. The name comes from its sensitivity to frost, the fronds dying quickly when first touched by it. It is sometimes treated as the only species in Onoclea, but some authors do not consider the genus monotypic.

<i>Gymnocarpium dryopteris</i> Species of fern

Gymnocarpium dryopteris, the western oakfern, common oak fern, oak fern, or northern oak fern, is a deciduous fern of the family Cystopteridaceae. It is widespread across much of North America and Eurasia. It has been found in Canada, the United States, Greenland, China, Japan, Korea, Russia, and most of Europe. It is a seedless, vascular plant that reproduces via spores and have a life cycle with alternating, free-living sporophyte and gametophyte phases.

<span class="mw-page-title-main">Prothallus</span> Gametophyte stage in the fern life cycle

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.

<span class="mw-page-title-main">Hymenophyllaceae</span> Family of ferns

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.

<span class="mw-page-title-main">Onocleaceae</span> Family of ferns

Onocleaceae is a small family of terrestrial ferns in the order Polypodiales. It is placed in the suborder Aspleniineae in the Pteridophyte Phylogeny Group classification of 2016. Alternatively, the family, along with Blechnaceae, may be placed in a very broadly defined family Aspleniaceae as the subfamily Blechnoideae. The family may contain from one to four genera, consisting of five species largely in north temperate climes. The four genera, Matteuccia, Onoclea, Onocleopsis and Pentarhizidium, may be included under the single genus Onoclea.

<i>Ceratopteris</i> Genus of aquatic plants

Ceratopteris is the only genus among homosporous ferns that is exclusively aquatic. It is pan-tropical and classified in the Parkerioideae subfamily of the family Pteridaceae.

<i>Aglaomorpha</i> (plant) Genus of ferns

Aglaomorpha is a genus of ferns in the subfamily Drynarioideae of the family Polypodiaceae. The Pteridophyte Phylogeny Group classification of 2016 uses this genus name, while other sources use Drynaria to include Aglaomorpha. Species are commonly known as basket ferns. As circumscribed in PPG I, the genus contains around 50 species.

<i>Notholaena standleyi</i> Species of fern

Notholaena standleyi, also known as star cloak fern and Standley's cloak fern, is a fern that is native to the United States and Mexico. It is a member of the genus Notholaena, which is part of the subfamily Cheilanthoideae of family Pteridaceae. It is distinguished by the pentagonal shape formed by the blades of its frond, a property other members of Notholaena do not possess.

<i>Hymenophyllum tunbrigense</i> Species of fern

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.

<i>Polyphlebium venosum</i> Species of fern

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 antarctica. 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. 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.

References

  1. Hassler, Michael (2004–2021). "Genus Lophosoria C.Presl". World Ferns. Synonymic Checklist and Distribution of Ferns and Lycophytes of the World. Version 12.3. Retrieved 2021-08-01.
  2. USDA, NRCS (n.d.). "Lophosoria quadripinnata". The PLANTS Database (plants.usda.gov). Greensboro, North Carolina: National Plant Data Team. Retrieved 2015-06-23.
  3. Dyer, A.F. 1979. "The culture of fern gametophytes for experimental investigation." p. 253-305. In A.F. Dyer (ed.) The experimental biology of ferns. Academic Press, Londres.
  4. Pichi Sermolli R. E. G. 1970. "Fragmenta Pteridologiae". -II. Webbia. 24: 699-722.
  5. 1 2 Wolf et al. 1999. "Phylogenetic relationships of the enigmatic fern families Hymenophyllopsidaceae and Lophosoriaceae: evidences from rbcL nucleotide sequences". Plant Syst. Evol. 219: 263-270
  6. Gastony G. J. y Tyron R. 1976. "Spore morphology in the Cyatheaceae". II. The genera Lophosoria, Metaxya, Sphaeropteris, Alsophila, and Nephelea. Amer J. Bot. 63: 738-758
  7. Pérez-García B., Fraile M. E., Mendoza A. 1995. "Desarrollo del gametofito del Lophosoria quadripinnata (Filicales: Lophosoriaceae)". Revista Biol. Trop. 43: 55-60.
  8. Kubitzki, K. 1990. Pteridophytes and Gymnosperms. en: K. V. Kramer. P. S. Green (Eds.) The families and genera of vascular plants. Vol 1. Springer-Verlag, Berlín, Alemania.
  9. Korall et al. 2006. "Tree ferns: Monophiletic groups and their relationships as revealed by four protein-coding plastid loci". Molecular phylogenetics and Evolution 39: 830-845.
  10. A. R. Smith, K. M. Pryer, E. Schuettpelz, P. Korall, H. Schneider, P. G. Wolf. 2006. "A classification for extant ferns". Taxonomy 55(3), 705-731 (pdf here Archived 2008-02-26 at the Wayback Machine )
  11. Stokey, A.G. 1930. "Prothallia of the Cyatheaceae." Bot. Gaz. (Crawfordsville) 90: 1-45.
  12. Rojas Alvarado A. F. 1996. "Aportes a la flora Pteridophyta costarricense". II. Taxones nuevos. Brenesia 45-46: 33-50
  13. 1 2 Dettmann M. E. 1986. "Significance of the Cretaceous-Tertiary spore genus Cyatheacidites in tracing the origin and migration of Lophosoria (Filicopsida). Special Papers in Palaeontology 35: 63-94.
  14. Cantrill D. J. 1998. "Early Cretaceous fern foliage from President Head, South Island, Antarctica. Alcheringa 22: 241-258
  15. Smith-Ramírez C. 1994. "Usos artesanales del bosque nativo. La extracción silenciosa", Revista Ambiente y Desarrollo, X, (2), 71-76 pdf here Archived 2007-10-21 at the Wayback Machine
  16. Hoffmann J. 1999. "El bosque chilote. Historia natural del archipiélago de Chiloé. Conservación y desarrollo sustentable de sus bosques y biodiversidad", Santiago: Defensores del Bosque Chileno| ISBN   956-7721-22-X

(in Spanish) Florachilena.cl