A fern (Polypodiopsida or Polypodiophyta /ˌpɒliˌpɒdiˈɒfɪtə, -əˈftə/) is a member of a group of vascular plants (plants with xylem and phloem) that reproduce via spores and have neither seeds nor flowers. The polypodiophytes include all living pteridophytes except the lycopods, and differ from mosses and other bryophytes 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.

Temporal range:
Fern diversity[2]
Scientific classification
Kingdom: Plantae
Clade: Tracheophytes
Clade: Euphyllophytes
Division: Polypodiophyta
Cronquist, Takhtajan & Zimmermann 1966
  • Filicatae Kubitski 1990
  • Filices
  • Filicophyta Endlicher 1836
  • Monilophyta Cantino & Donoghue 2007
  • Pteridopsida Ritgen 1828

Ferns have complex leaves called megaphylls, that are more complex than 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.

Ferns first appear in the fossil record about 360 million years ago in the late Devonian period, but many of the current families and species did not appear until roughly 145 million years ago in the early Cretaceous, after flowering plants came to dominate many environments. The fern Osmunda claytoniana is a paramount example of evolutionary stasis; paleontological evidence indicates it has remained unchanged, even at the level of fossilized nuclei and chromosomes, for at least 180 million years.

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 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.


A fern unrolling a young frond
Tree ferns, probably Dicksonia antarctica, growing in Nunniong, Australia
Tree ferns, Alsophila spinulosa, growing at Xitou Nature Education Area, Taiwan
Sporophylls of Acrostichum aureum

Extant ferns are herbaceous perennials and most lack woody growth.[4] Their foliage may be deciduous or evergreen,[5] and some are semi-evergreen depending on the climate.[6] Like the sporophytes of seed plants, those of ferns consist of stems, leaves and roots. Ferns differ from seed plants in reproducing by spores. 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 the maternal gametophyte.


Fern stems are often referred to as 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). These can reach up to 20 meters (66 ft) tall in a few species (e.g., Cyathea brownii on Norfolk Island and Cyathea medullaris in New Zealand).[7]


The green, photosynthetic part of the plant is technically a megaphyll and in ferns, it is often referred to as a frond. New leaves typically expand by the unrolling of a tight spiral called a crozier or fiddlehead into fronds.[8] 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. In monomorphic ferns, the fertile and sterile leaves looks morphologically the same, and are photosynthesizing in the same way. In hemidimorphic ferns, just a portion of the fertile leaf is different from the sterile leaves. And in dimorphic ferns, also called holomorphic ferns, the two types of leaves are morphologically distinct (frond dimorphism).[9] The fertile leaves are much narrower than the sterile leaves, and may even have no green tissue at all (e.g., Blechnaceae, 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 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.[10][11] 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 the stipe are known as pinnae and are often again divided into smaller pinnules.[12]


The underground non-photosynthetic structures that take up water and nutrients from soil. They are always fibrous and structurally are very similar to the roots of seed plants.

As in all other 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 the spore wall and are dependent on the parent sporophyte for their nutrition. A fern gametophyte typically consists of:

  • Prothallus: A green, photosynthetic structure that is one cell thick, usually heart or kidney shaped, 3–10 mm long and 2–8 mm broad. The prothallus produces gametes by means of:
    • Antheridia: Small spherical structures that produce flagellate sperm.
    • Archegonia: A flask-shaped structure that produces a single egg at the bottom, reached by the sperm by swimming down the neck.
  • Rhizoids: root-like structures (not true roots) that consist of single greatly elongated cells, that absorb water and mineral salts over the whole structure. Rhizoids anchor the prothallus to the soil.


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).[13][14][15] By 1806 this had increased to 38 genera,[16] and has progressively increased since (see Schuettpelz et al (2018) Figure 1). Ferns were traditionally classified in 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 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 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 is polyphyletic, the term fern allies should be abandoned, except in a historical context.[17] 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, the whisk ferns and ophioglossoid ferns are demonstrably a clade, and the horsetails and Marattiaceae are arguably another clade.

Molecular phylogenetics

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:[18]

Molecular data, which remain poorly constrained for many parts of the plants' phylogeny, have been supplemented by morphological observations supporting the inclusion of Equisetaceae in the ferns, notably relating to the construction of their sperm and peculiarities of their roots.[18] However, there remained differences of opinion about the placement of the genus Equisetum (see Equisetopsida for further discussion). One possible solution was to denominate only the leptosporangiate ferns as "true ferns" while denominating the other three groups as fern allies. In practice, numerous classification schemes have been proposed for ferns and fern allies, and there has been little consensus among them.

The leptosporangiate ferns are sometimes called "true ferns".[19] 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 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".[20] Grewe et al. (2013) confirmed the inclusion of horsetails within ferns sensu lato, but also suggested that uncertainties remained in their precise placement.[21] Other classifications have raised Ophioglossales to the rank of a fifth class, separating the whisk ferns and ophioglossoid ferns.[21]

One problem with the classification of ferns is that of cryptic species. A cryptic species is a species that is morphologically similar to another species, but differs genetically in ways that prevent fertile interbreeding. A good example of this is the currently designated species Asplenium trichomanes (maidenhair spleenwort). This is actually a species complex that includes distinct diploid and tetraploid races. There are minor but unclear morphological differences between the two groups, which prefer distinctly differing habitats. In many cases such as this, the species complexes have been separated into separate species, thus raising the total number of species of ferns. Many more cryptic species may be yet to be discovered and designated.


The ferns are related to other higher order taxa as shown in the following cladogram:[17][22][23][3]


Lycopodiophyta (Lycopodiopsida) - lycophytes


Polypodiophyta (Polypodiopsida) - ferns



Angiospermae - flowering plants

(seed plants)
 (vascular plants) 

Nomenclature and subdivision

The classification of Smith et al. (2006) treated ferns as four classes:[18][24]

In addition they defined 11 orders and 37 families.[18] That system was a consensus of a number of studies, and was further refined.[21][25] The phylogenetic relationships are shown in the following cladogram (to the level of orders).[18][26][21] This division into four major clades was then confirmed using morphology alone.[27]


Lycopodiophytes (club mosses, spike mosses, quillworts)


Spermatophytes (seed plants)


Psilotales (whisk ferns)

Ophioglossales (grapeferns etc.)


Equisetales (horsetails)





Hymenophyllales (filmy ferns)



Salviniales (heterosporous)

Cyatheales (tree ferns)



Subsequently, Chase and Reveal considered both lycopods and ferns as subclasses of 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).[23] Christenhusz et al.[lower-alpha 1] (2011) followed this use of subclasses but recombined Smith's Psilotopsida as Ophioglossidae, giving four subclasses of ferns again.[28]

Christenhusz and Chase (2014) developed 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;[17]

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 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:

Christenhusz and Chase 2014 [3] Nitta et al. 2022[29] and Fern Tree of life[30]






























In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the Polypodiopsida consist of four subclasses, 11 orders, 48 families, 319 genera, and an estimated 10,578 species.[31] Thus Polypodiopsida in the broad sense (sensu lato) as used by the PPG (Polypodiopsida sensu PPG I) needs to be distinguished from the narrower usage (sensu stricto) of Smith et al. (Polypodiopsida sensu Smith et al.)[3] Classification of ferns remains unresolved and controversial with competing viewpoints (splitting vs lumping) between the systems of the PPG on the one hand and Christenhusz and Chase on the other, respectively. In 2018, Christenhusz and Chase explicitly argued against recognizing as many genera as PPG I.[15][32]

Comparison of fern subdivisions in some classifications
Smith et al. (2006)[18]Chase & Reveal (2009)[23]Christenhusz et al. (2011)[28]Christenhusz & Chase (2014, 2018)[17][33]PPG I (2016)[3]
(no rank)
(no rank)
ferns (monilophytes)
(no rank)
ferns (Polypodiophyta)
(no rank)
 Class Polypodiopsida
Class Equisetopsida  Subclass Equisetidae  Subclass Equisetidae  Subclass Equisetidae Subclass Equisetidae
Class Psilotopsida  Subclass Ophioglossidae
  Subclass Psilotidae
  Subclass Ophioglossidae  Subclass Ophioglossidae Subclass Ophioglossidae
Class Marattiopsida  Subclass Marattiidae  Subclass Marattiidae  Subclass Marattiidae Subclass Marattiidae
Class Polypodiopsida  Subclass Polypodiidae  Subclass Polypodiidae  Subclass Polypodiidae Subclass Polypodiidae

Evolution and biogeography

Fern-like taxa (Wattieza) first appear in the fossil record in the middle Devonian period, ca. 390 Mya. By the Triassic, the first evidence of ferns related to several modern families appeared. The great fern radiation occurred in the late Cretaceous, when many modern families of ferns first appeared.[34][1][35][36] Ferns evolved to cope with low-light conditions present under the canopy of angiosperms.

Remarkably, the photoreceptor neochrome in the two orders Cyatheales and Polypodiales, integral to their adaptation to low-light conditions, was obtained via horizontal gene transfer from hornworts, a bryophyte lineage.[37]

Due to the very large genome seen in most ferns, it was suspected they might had gone through whole genome duplications, but DNA sequencing has shown that their genome size is caused by the accumulation of mobile DNA like transposons and other genetic elements that infect genomes and get copied over and over again.[38]

Distribution and habitat

Ferns are widespread in their distribution, with the greatest richness in the tropics and least in arctic areas. The greatest diversity occurs in tropical rainforests.[39] New Zealand, for which the fern is a symbol, has about 230 species, distributed throughout the country.[40]


Ferns at Muir Woods, California

Fern species live in a wide variety of habitats, from remote mountain elevations, to dry desert rock faces, bodies of water or open fields. Ferns in general may be thought of as largely being specialists in marginal habitats, often succeeding in places where various environmental factors limit the success of flowering plants. Some ferns are among the world's most serious weed species, including the bracken fern growing in the Scottish highlands, or the mosquito fern (Azolla) growing in tropical lakes, both species forming large aggressively spreading colonies. There are four particular types of habitats that ferns are found in: moist, shady forests; crevices in rock faces, especially when sheltered from the full sun; acid wetlands including bogs and swamps; and tropical trees, where many species are epiphytes (something like a quarter to a third of all fern species).[41]

Especially the epiphytic ferns have turned out to be hosts of a huge diversity of invertebrates. It is assumed that bird's-nest ferns alone contain up to half the invertebrate biomass within a hectare of rainforest canopy.[42]

Many ferns depend on associations with mycorrhizal fungi. Many ferns grow only within specific pH ranges; for instance, the climbing fern (Lygodium palmatum) of eastern North America will grow only in moist, intensely acid soils, while the bulblet bladder fern (Cystopteris bulbifera), with an overlapping range, is found only on limestone.

The spores are rich in lipids, protein and calories, so some vertebrates eat these. The European woodmouse (Apodemus sylvaticus) has been found to eat the spores of Culcita macrocarpa, and the bullfinch (Pyrrhula murina) and the New Zealand lesser short-tailed bat (Mystacina tuberculata) also eat fern spores.[43]

Life cycle

Close-up of a monarch fern sorus, showing its sporangium
Gametophyte (thalloid green mass) and sporophyte (ascendent frond) of Onoclea sensibilis

Ferns are vascular plants differing from lycophytes by having true leaves (megaphylls), which are often pinnate. They differ from seed plants (gymnosperms and angiosperms) in reproducing by means of spores and lacking flowers and seeds. Like all land plants, they have a life cycle referred to as alternation of generations, characterized by alternating diploid sporophytic and haploid gametophytic phases. The diploid sporophyte has 2n paired chromosomes, where n varies from species to species. The haploid gametophyte has n unpaired chromosomes, i.e. half the number of the sporophyte. The gametophyte of ferns is a free-living organism, whereas the gametophyte of the gymnosperms and angiosperms is dependent on the sporophyte.

The life cycle of a typical fern proceeds as follows:

  1. A diploid sporophyte phase produces haploid spores by meiosis (a process of cell division which reduces the number of chromosomes by a half).
  2. A spore grows into a free-living haploid gametophyte by mitosis (a process of cell division which maintains the number of chromosomes). The gametophyte typically consists of a photosynthetic prothallus.
  3. The gametophyte produces gametes (often both sperm and eggs on the same prothallus) by mitosis.
  4. A mobile, flagellate sperm fertilizes an egg that remains attached to the prothallus.
  5. The fertilized egg is now a diploid zygote and grows by mitosis into a diploid sporophyte (the typical fern plant).


Ferns are not as important economically as seed plants, but have considerable importance in some societies. Some ferns are used for food, including the fiddleheads of Pteridium aquilinum (bracken), Matteuccia struthiopteris (ostrich fern), and Osmundastrum cinnamomeum (cinnamon fern). Diplazium esculentum is also used in the tropics (for example in budu pakis, a traditional dish of Brunei[44]) as food. Tubers from the "para", Ptisana salicina (king fern) are a traditional food in New Zealand and the South Pacific. Fern tubers were used for food 30,000 years ago in Europe.[45][46] Fern tubers were used by the Guanches to make gofio in the Canary Islands. Ferns are generally not known to be poisonous to humans.[47] Licorice fern rhizomes were chewed by the natives of the Pacific Northwest for their flavor.[48]

Ferns of the genus Azolla, commonly known as water fern or mosquito ferns are very small, floating plants that do not resemble ferns. The mosquito ferns are used as a biological fertilizer in the rice paddies of southeast Asia, taking advantage of their ability to fix nitrogen from the air into compounds that can then be used by other plants.

Ferns have proved resistant to phytophagous insects. The gene that express the protein Tma12 in an edible fern, Tectaria macrodonta, has been transferred to cotton plants, which became resistant to whitefly infestations.[49]

Many ferns are grown in horticulture as landscape plants, for cut foliage and as houseplants, especially the Boston fern (Nephrolepis exaltata) and other members of the genus Nephrolepis. The bird's nest fern (Asplenium nidus) is also popular, as are the staghorn ferns (genus Platycerium). Perennial (also known as hardy) ferns planted in gardens in the northern hemisphere also have a considerable following.

Several ferns, such as bracken[50] and Azolla[51] species are noxious weeds or invasive species. Further examples include Japanese climbing fern (Lygodium japonicum), sensitive fern (Onoclea sensibilis) and Giant water fern (Salvinia molesta), one of the world's worst aquatic weeds.[52] The important fossil fuel coal consists of the remains of primitive plants, including ferns.

Ferns have been studied and found to be useful in the removal of heavy metals, especially arsenic, from the soil. Other ferns with some economic significance include:

  • Dryopteris filix-mas (male fern), used as a vermifuge, and formerly in the US Pharmacopeia; also, this fern accidentally sprouting in a bottle resulted in Nathaniel Bagshaw Ward's 1829 invention of the terrarium or Wardian case
  • Rumohra adiantiformis (floral fern), extensively used in the florist trade
  • Microsorum pteropus (Java fern), one of the most popular freshwater aquarium plants.
  • Osmunda regalis (royal fern) and Osmunda cinnamomea (cinnamon fern), the root fiber being used horticulturally; the fiddleheads of O. cinnamomea are also used as a cooked vegetable
  • Matteuccia struthiopteris (ostrich fern), the fiddleheads used as a cooked vegetable in North America
  • Pteridium aquilinum and Pteridium esculentum (bracken), the fiddleheads used as a cooked vegetable in Japan and are believed to be responsible for the high rate of stomach cancer in Japan. It is also one of the world's most important agricultural weeds, especially in the British highlands, and often poisons cattle and horses.
  • Diplazium esculentum (vegetable fern), a source of food for some societies
  • Pteris vittata (brake fern), used to absorb arsenic from the soil
  • Polypodium glycyrrhiza (licorice fern), roots chewed for their pleasant flavor
  • Tree ferns, used as building material in some tropical areas
  • Cyathea cooperi (Australian tree fern), an important invasive species in Hawaii
  • Ceratopteris richardii, a model plant for teaching and research, often called C-fern


Blätter des Manns Walfarn. by Alois Auer, Vienna: Imperial Printing Office, 1853


The study of ferns and other pteridophytes is called pteridology. A pteridologist is a specialist in the study of pteridophytes in a broader sense that includes the more distantly related lycophytes.


Pteridomania is a term for the Victorian era craze of fern collecting and fern motifs in decorative art including pottery, glass, metals, textiles, wood, printed paper, and sculpture "appearing on everything from christening presents to gravestones and memorials." The fashion for growing ferns indoors led to the development of the Wardian case, a glazed cabinet that would exclude air pollutants and maintain the necessary humidity.[53]

Barnsley fern created using a chaos game, through an Iterated function system (IFS).

The dried form of ferns was also used in other arts, being used as a stencil or directly inked for use in a design. The botanical work, The Ferns of Great Britain and Ireland, is a notable example of this type of nature printing. The process, patented by the artist and publisher Henry Bradbury, impressed a specimen on to a soft lead plate. The first publication to demonstrate this was Alois Auer's The Discovery of the Nature Printing-Process.

Fern bars were popular in America in the 1970s and 80s.


Ferns figure in folklore, for example in legends about mythical flowers or seeds.[54] In Slavic folklore, ferns are believed to bloom once a year, during the Ivan Kupala night. Although alleged to be exceedingly difficult to find, anyone who sees a fern flower is thought to be guaranteed to be happy and rich for the rest of their life. Similarly, Finnish tradition holds that one who finds the seed of a fern in bloom on Midsummer night will, by possession of it, be guided and be able to travel invisibly to the locations where eternally blazing Will o' the wisps called aarnivalkea mark the spot of hidden treasure. These spots are protected by a spell that prevents anyone but the fern-seed holder from ever knowing their locations.[55] In the US, ferns are thought to have magical properties such as a dried fern can be thrown into hot coals of a fire to exorcise evil spirits, or smoke from a burning fern is thought to drive away snakes and such creatures.[56]

New Zealand

Ferns are the national emblem of New Zealand and feature on its passport and in the design of its national airline, Air New Zealand, and its rugby team, the All Blacks.

Organisms confused with ferns


Several non-fern plants (and even animals) are called ferns and are sometimes confused with ferns. These include:

Fern-like flowering plants

Some flowering plants such as palms and members of the carrot family have pinnate leaves that somewhat resemble fern fronds. However, these plants have fully developed seeds contained in fruits, rather than the microscopic spores of ferns.

See also


  1. President, International Association of Pteridologists


  1. Stein et al 2007.
  2. a: Adiantum capillus-veneris (Pteridaceae); b: Sceptridium japonicum (Ophioglossaceae); c: Hypolepis punctata (Dennstaedtiaceae); d: Lygodium japonicum (Lygodiaceae); e: Equisetum hyemale (Equisetaceae); f: Woodwardia orientalis (Blechnaceae); g: Azolla filiculoides and Salvinia natans (Salviniaceae); h: Dryopteris erythrosora (Dryopteridaceae); i: Deparia japonica (Athyriaceae); j: Psilotum nudum (Psilotaceae); k: Odontosoria chinensis (Lindsaeaceae); l: Dicranopteris linearis (Gleicheniaceae); m: Phegopteris decursivepinnata (Thelypteridaceae); n: Asplenium nidus (Aspleniaceae); o: Osmunda japonica (Osmundaceae); p: Davallia mariesii (Davalliaceae); q: Hymenophyllum sp. (Hymenophyllaceae); r: Matteuccia struthiopteris (Onocleaceae); s: Lemmaphyllum microphyllum (Polypodiaceae); t: Angiopteris lygodiifolia (Marattiidae) and u: Marsilea quadrifolia (Marsileaceae).
  3. Pteridophyte Phylogeny Group 2016.
  4. Mauseth, James D. (September 2008). Botany: an Introduction to Plant Biology. Jones & Bartlett Publishers. ISBN 978-1-4496-4720-9.
  5. Fernández, Helena; Kumar, Ashwani; Revilla, Maria Angeles (11 November 2010). Working with Ferns: Issues and Applications. Springer Science & Business Media. ISBN 978-1-4419-7162-3.
  6. Hodgson, Larry (1 January 2005). Making the Most of Shade: How to Plan, Plant, and Grow a Fabulous Garden that Lightens Up the Shadows. Rodale. ISBN 978-1-57954-966-4.
  7. Large, Mark F.; Braggins, John E. (2004). Tree Ferns. Timber Press. ISBN 0881926302.
  8. McCausland 2019.
  9. Understanding the contribution of LFY and PEBP flowering genes to fern leaf dimorphism - Botany 2019
  10. Fern Structure - Forest Service
  11. Fern Structure - Forest Service
  12. "Fern Fronds". Basic Biology. Archived from the original on 19 April 2015. Retrieved 6 December 2014.
  13. Underwood 1903.
  14. Linnaeus 1753.
  15. Schuettpelz et al 2018.
  16. Swartz 1806.
  17. Christenhusz & Chase 2014.
  18. Smith et al.2006.
  19. Stace, Clive (2010b). New Flora of the British Isles (3rd ed.). Cambridge, UK: Cambridge University Press. p. xxviii. ISBN 978-0-521-70772-5.
  20. Rai, Hardeep S. & Graham, Sean W. (2010). "Utility of a large, multigene plastid data set in inferring higher-order relationships in ferns and relatives (monilophytes)". American Journal of Botany. 97 (9): 1444–1456. doi:10.3732/ajb.0900305. PMID 21616899., p. 1450
  21. Grewe, Felix; et al. (2013). "Complete plastid genomes from Ophioglossum californicum, Psilotum nudum, and Equisetum hyemale reveal an ancestral land plant genome structure and resolve the position of Equisetales among monilophytes". BMC Evolutionary Biology. 13 (1): 1–16. doi:10.1186/1471-2148-13-8. ISSN 1471-2148. PMC 3553075. PMID 23311954.
  22. Cantino et al 2007.
  23. Chase & Reveal 2009.
  24. Schuettpelz 2007, Table I.
  25. Karol, Kenneth G; et al. (2010). "Complete plastome sequences of Equisetum arvense and Isoetes flaccida: implications for phylogeny and plastid genome evolution of early land plant lineages". BMC Evolutionary Biology. 10 (1): 321–336. doi:10.1186/1471-2148-10-321. ISSN 1471-2148. PMC 3087542. PMID 20969798.
  26. Li, F-W; Kuo, L-Y; Rothfels, CJ; Ebihara, A; Chiou, W-L; et al. (2011). "rbcL and matK Earn Two Thumbs Up as the Core DNA Barcode for Ferns". PLOS ONE. 6 (10): e26597. Bibcode:2011PLoSO...626597L. doi:10.1371/journal.pone.0026597. PMC 3197659. PMID 22028918.
  27. Schneider et al 2009.
  28. Christenhusz et al 2011.
  29. Nitta, Joel H.; Schuettpelz, Eric; Ramírez-Barahona, Santiago; Iwasaki, Wataru; et al. (2022). "An Open and Continuously Updated Fern Tree of Life". Frontiers in Plant Science. 13. doi:10.3389/fpls.2022.909768.
  30. "Tree viewer: interactive visualization of FTOL". FTOL v1.3.0. 2022. Retrieved 12 December 2022.
  31. Christenhusz & Byng 2016.
  32. Christenhusz & Chase 2018.
  33. Christenhusz et al 2018.
  34. UCMP 2019.
  35. Berry 2009.
  36. Bomfleur et al 2014.
  37. Li, F.-W.; Villarreal, J. C.; Kelly, S.; Rothfels, C. J.; Melkonian, M.; Frangedakis, E.; Ruhsam, M.; Sigel, E. M.; Der, J. P.; Pittermann, J.; Burge, D. O.; Pokorny, L.; Larsson, A.; Chen, T.; Weststrand, S.; Thomas, P.; Carpenter, E.; Zhang, Y.; Tian, Z.; Chen, L.; Yan, Z.; Zhu, Y.; Sun, X.; Wang, J.; Stevenson, D. W.; Crandall-Stotler, B. J.; Shaw, A. J.; Deyholos, M. K.; Soltis, D. E.; Graham, S. W.; Windham, M. D.; Langdale, J. A.; Wong, G. K.-S.; Mathews, S.; Pryer, K. M. (6 May 2014). "Horizontal transfer of an adaptive chimeric photoreceptor from bryophytes to ferns". Proceedings of the National Academy of Sciences. 111 (18): 6672–6677. Bibcode:2014PNAS..111.6672L. doi:10.1073/pnas.1319929111. PMC 4020063. PMID 24733898.
  38. Genes for seeds arose early in plant evolution, ferns reveal
  39. EB 2019.
  40. SLH 2018.
  41. Schuettpelz 2007, Part I.
  42. "Ferns Brimming With Life". Science | AAAS. 2 June 2004.
  43. Walker, Matt (19 February 2010). "A mouse that eats ferns like a dinosaur". BBC Earth News. Retrieved 20 February 2010.
  44. Indigenous Fermented Foods of Southeast Asia. 2015.
  45. "Stone Age humans liked their burgers in a bun", Sonia Van Gilder Cooke, New Scientist, 23 October 2010, p. 18.
  46. "Thirty thousand-year-old evidence of plant food processing" by Anna Revedin et al., PNAS, published online 18 October 2010.
  47. Pelton, Robert (2011). The Official Pocket Edible Plant Survival Manual. Freedom and Liberty Foundation Press. p. 25. BNID 2940013382145.
  48. Moerman, Daniel E. (27 October 2010). Native American Food Plants: An Ethnobotanical Dictionary. Timber Press. p. 190. ISBN 978-1-60469-189-4.
  49. Shukla, Anoop Kumar; Upadhyay, Santosh Kumar; Mishra, Manisha; Saurabh, Sharad; Singh, Rahul; Singh, Harpal; Thakur, Nidhi; Rai, Preeti; Pandey, Paras; Hans, Aradhana L.; Srivastava, Subhi; Rajapure, Vikram; Yadav, Sunil Kumar; Singh, Mithlesh Kumar; Kumar, Jitendra; Chandrashekar, K.; Verma, Praveen C.; Singh, Ajit Pratap; Nair, K. N.; Bhadauria, Smrati; Wahajuddin, Muhammad; Singh, Sarika; Sharma, Sharad; Omkar, null; Upadhyay, Ram Sanmukh; Ranade, Shirish A.; Tuli, Rakesh; Singh, Pradhyumna Kumar (26 October 2016). "Expression of an insecticidal fern protein in cotton protects against whitefly". Nature Biotechnology. 34 (10): 1046–1051. doi:10.1038/nbt.3665. PMID 27598229. S2CID 384923.
  50. "Datasheet: Pteridium aquilinum (bracken)". CAB International. 2018. Retrieved 11 February 2019.
  51. "Datasheet: Azolla filiculoides (water fern)". CAB International. 2018. Retrieved 11 February 2019.
  52. Moran, Robbin (2004). A Natural History of Ferns. ISBN 0-88192-667-1.
  53. Boyd, Peter D. A. (2 January 2002). "Pteridomania - the Victorian passion for ferns". Revised: web version. Antique Collecting 28, 6, 9–12. Retrieved 2 October 2007. {{cite journal}}: Cite journal requires |journal= (help)
  54. May 1978.
  55. "Traditional Finnish Midsummer celebration". Saunalahti.fi. Retrieved 7 September 2013.
  56. Cunningham, Scott (1999). Cunningham's Encyclopedia of Magical Herbs. Llewellyn. p. 102.


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