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Fern

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Ferns (Pteridophyta)
Temporal range: Mid Devonian[1] - Recent
Polystichum setiferum unrolling young frond
Scientific classification
Kingdom:
Division:
Pteridophyta
Classes[2]

A fern is any one of a group of about 20,000 species of plants classified in the phylum or division Pteridophyta, also known as Filicophyta. The group is also referred to as polypodiophyta, or polypodiopsida when treated as a subdivision of tracheophyta (vascular plants). The study of ferns and other pteridophytes is called pteridology, and one who studies ferns and other pteridophytes is called a pteridologist. The term "pteridophyte" has traditionally been used to describe all seedless vascular plants, making it synonymous with "ferns and fern allies". This can be confusing since members of the fern phylum Pteridophyta are also sometimes referred to as pteridophytes.

Life cycle

Ferns are vascular plants differing from the more primitive lycophytes by having true leaves (megaphylls), and they differ from seed plants (gymnosperms and angiosperms) in their mode of reproduction - lacking flowers and seeds. Like all other vascular plants, they have a life cycle referred to as alternation of generations, characterized by a diploid sporophytic and a haploid gametophytic phase. Unlike the gymnosperms and angiosperms, the ferns' gametophyte is a free-living organism. The life cycle of a typical fern is as follows:

  1. A sporophyte (diploid) phase produces haploid spores by meiosis;
  2. A spore grows by cell division into a gametophyte, which 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 sporophyte (the typical "fern" plant).

Fern ecology

Ferns at Muir Woods, California

The popular image of ferns growing in moist shady woodland nooks, is far from being a complete picture of the habitats where ferns can be found growing. Fern species live in a wide variety of habitats, from remote mountain elevations, to dry desert rock faces, to bodies of water or in 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 British highlands, or the mosquito fern (Azolla) growing in tropical lakes, both species form 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.

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

Fern structure

Ferns at the Royal Melbourne Botanical Gardens
Tree ferns, probably Dicksonia antarctica, growing in Nunniong, Australia

Like the sporophytes of seed plants, those of ferns consist of:

  • Stems: Most often an underground creeping rhizome, but sometimes an above-ground creeping stolon (e.g., Polypodiaceae), or an above-ground erect semi-woody trunk (e.g., Cyatheaceae) reaching up to 20 m in a few species (e.g., Cyathea brownii on Norfolk Island and Cyathea medullaris in New Zealand).
  • Leaf: The green, photosynthetic part of the plant. In ferns, it is often referred to as a frond, but this is because of the historical division between people who study ferns and people who study seed plants, rather than because of differences in structure. New leaves typically expand by the unrolling of a tight spiral called a crozier or fiddlehead. This uncurling of the leaf is termed circinate vernation. Leaves are divided into three types:
    • Trophophyll: A leaf that does not produce spores, instead only producing sugars by photosynthesis. Analogous to the typical green leaves of seed plants.
    • Sporophyll: A leaf that produces spores. These leaves are analogous to the scales of pine cones or to stamens and pistil in gymnosperms and angiosperms, respectively. Unlike the seed plants, however, the sporophylls of ferns are typically not very specialized, looking similar to trophophylls and producing sugars by photosynthesis as the trophophylls do.
    • Brophophyll: A leaf that produces abnormally large amounts of spores. There leaves are also larger than the other leaves but bare a resemblance to trophopylls.
  • Roots: The 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.

The gametophytes of ferns, however, are very different from those of seed plants. They typically consist 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, water and mineral salts are absorbed over the whole structure. Rhizoids anchor the prothallus to the soil.

One interesting difference between sporophytes and gametophytes might be summed up by the saying that "Nothing eats ferns, but everything eats gametophytes." This is an over-simplification, but it is true that gametophytes are often difficult to find in the field because they are far more likely to be food than are the sporophytes.

Evolution and classification

Ferns first appear in the fossil record in the early-Carboniferous period. 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.

Ferns have traditionally been grouped in the Class Filices, but modern classifications assign them their own division in the plant kingdom, called Pteridophyta.

Traditionally, three discrete groups of plants have been considered ferns: two groups of eusporangiate ferns--families Ophioglossaceae (adders-tongues, moonworts, and grape-ferns) and Marattiaceae--and the leptosporangiate ferns. The Marattiaceae are a primitive group of tropical ferns with a large, fleshy rhizome, and are now thought to be a sibling taxon to the main group of ferns, the leptosporangiate ferns. Several other groups of plants were considered "fern allies": the clubmosses, spikemosses, and quillworts in the Lycopodiophyta, the whisk ferns in Psilotaceae, and the horsetails in the Equisetaceae. More recent genetic studies have shown that the Lycopodiophyta are only distantly related to any other vascular plants, having radiated evolutionarily at the base of the vascular plant clade, while both the whisk ferns and horsetails are as much "true" ferns as are the Ophioglossoids and Marattiaceae. In fact, the whisk ferns and Ophioglossoids are demonstrably a clade, and the horsetails and Marattiaceae are arguably another clade. Molecular data - which remain poorly constrained for many parts of the plants' phylogeny - have been supplemented by recent morphological observations supporting the inclusion of Equisetaceae within the ferns, notably relating to the construction of their sperm, and peculiarities of their roots (Smith et al 2006, and references therein).

One possible means of treating this situation is to consider only the leptosporangiate ferns as "true" ferns, while considering 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. A new classification by Smith et al. (2006) is based on recent molecular systematic studies, in addition to morphological data. This classification divides ferns into four classes:

  • Psilotopsida
  • Equisetopsida
  • Marattiopsida
  • Polypodiopsida

The last 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.

The complete classification scheme proposed by Smith et al. (2006; alternative names in brackets):

Economic uses

Ferns are not as important economically as seed plants but have considerable importance. Some ferns are used for food, including the fiddleheads of bracken, Pteridium aquilinum, ostrich fern, Matteuccia struthiopteris, and cinnamon fern, Osmunda cinnamomea]. Diplazium esculentum is also used by some tropical peoples as food.

Ferns of the genus Azolla are very small, floating plants that do not look like ferns. Called mosquito fern, they 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.

A great many ferns are grown in horticulture as landscape plants, for cut foliage and as houseplants, especially the Boston fern (Nephrolepis exaltata). The bird's-nest fern, Asplenium nidus, is also popular, and the staghorn ferns, genus Platycerium, have a considerable following.

Several ferns are noxious weeds or invasive species, including Japanese climbing fern (Lygodium japonicum), mosquito fern and sensitive fern (Onoclea sensibilis). Giant water fern (Salvinia molesta) is one of the world's worst aquatic weeds. The important fossil fuel coal consists of the remains of primitive plants, including ferns.

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 adiantoides (floral fern), extensively used in the florist trade
  • 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 (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 native 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

Cultural connotations

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

In Slavic folklore, ferns are believed to bloom once a year, during the Ivan Kupala night. Although it's exceedingly difficult to find, anyone who takes a look of a fern flower will be happy and rich for the rest of his life. Similarly in Finland, the tradition holds that one who finds the seed of a fern in bloom on Midsummer night, will by the possession of it be able to travel under a glamour of invisibility and shall be guided to the locations where eternally blazing Will o' the wisps mark the spot of hidden treasure caches[citation needed].

Ferns were popular as a decorative motif in Victorian England, the designs frequently appeared on crockery, glassware, cast iron objects, and textiles. 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.

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

The dried form of ferns was also used in other arts, being used 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.

Misunderstood names

Several non-fern plants are called "ferns" and are sometimes confused with true ferns. These include:

  • "Asparagus fern" - This may apply to one of several species of the monocot genus Asparagus, which are flowering plants.
  • "Sweetfern" - A flowering shrub of the genus Comptonia.
  • "Air fern" - A group of animals called hydrozoan that are distantly related to jellyfish and corals. They are harvested, dried, dyed green, and then sold as a "plant" that can "live on air". While it may look like a fern, it is merely the skeleton of this colonial animal.

In addition, the book Where the Red Fern Grows has elicited many questions about the mythical "red fern" named in the book. There is no such known plant, although there has been speculation that the oblique grape-fern, Sceptridium dissectum, could be referred to here, because it is known to appear on disturbed sites and its fronds may redden over the winter.

See also

References

  1. ^ Wattieza, Stein, W. E., F. Mannolini, L. V. Hernick, E. Landling, and C. M. Berry. 2007. "Giant cladoxylopsid trees resolve the enigma of the Earth's earliest forest stumps at Gilboa", Nature (19 April 2007) 446:904-907.
  2. ^ Smith, A.R. (2006). "A classification for extant ferns" (PDF). Taxon. 55 (3): 705–731. Retrieved 2008-02-12. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  • Pryer, Kathleen M., Harald Schneider, Alan R. Smith, Raymond Cranfill, Paul G. Wolf, Jeffrey S. Hunt and Sedonia D. Sipes. 2001. Horsetails and ferns are a monophyletic group and the closest living relatives to seed plants. Nature 409: 618-622 (abstract here).
  • Pryer, Kathleen M., Eric Schuettpelz, Paul G. Wolf, Harald Schneider, Alan R. Smith and Raymond Cranfill. 2004. Phylogeny and evolution of ferns (monilophytes) with a focus on the early leptosporangiate divergences. American Journal of Botany 91:1582-1598 (online abstract here).
  • Moran, Robbin C. (2004). A Natural History of Ferns. Portland, OR: Timber Press. ISBN 0-88192-667-1.
  • Lord, Thomas R. (2006). Ferns and Fern Allies of Pennsylvania. Indiana, PA: Pinelands Press. [1]
  • Smith, A. R., K. M. Pryer, E. Schuettpelz, P. Korall, H. Schneider & P. G. Wolf. 2006. A classification for extant ferns. Taxon 55(3):705–731.online available
  • Boyd, Peter D. A. (2002-01-02). "Pteridomania - the Victorian passion for ferns". Revised: web version. Antique Collecting 28, 6, 9-12. Retrieved 2007-10-02. {{cite journal}}: Cite journal requires |journal= (help)

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