Dennstaedtiaceae

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Dennstaedtiaceae
Temporal range: Cenomanian–Recent
Fern dsc06699.jpg
Pteridium aquilinum
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Division: Polypodiophyta
Class: Polypodiopsida
Order: Polypodiales
Suborder: Dennstaedtiineae
Schwarstb. & Hovenkamp
Family: Dennstaedtiaceae
Lotsy
Genera [1]
Synonyms
  • Hypolepidaceae Pichi-Sermolli 1970
  • Monachosoraceae Ching 1978
  • Pteridiaceae Ching 1975

Dennstaedtiaceae is one of fifteen families in the order Polypodiales, the most derived families within monilophytes (ferns). It comprises 10 genera with ca 240 known species, [2] including one of the world's most abundant ferns, Pteridium aquilinum (bracken). Members of the order generally have large, highly divided leaves and have either small, round intramarginal sori with cup-shaped indusia (e.g. Dennstaedtia) or linear marginal sori with a false indusium formed from the reflexed leaf margin (e.g. Pteridium). The morphological diversity among members of the order has confused past taxonomy, but recent molecular studies have supported the monophyly of the order and the family. [3] The reclassification of Dennstaedtiaceae and the rest of the monilophytes was published in 2006, [3] so most of the available literature is not updated.

Contents


Distribution of genera

Generally, the family is pantropical, but due to the distribution of Pteridium (the most widespread fern genus), Dennstaedtiaceae can be found worldwide. [4] Pteridium is a well adapted early successional genus, generally described as a weed because of its ease of spread. The spore is light and robust, so it can travel relatively far and colonise open, disturbed environments easily. [5] Dennstaedtia is mostly tropical to warm-temperate, but not well represented in the Amazon or Africa. Oenotrichia is in New Caledonia. Leptolepia is in New Zealand, Queensland (Australia), and in New Guinea. Microlepia is in the Asiatic-Pacific. Paesia occurs in tropical America, Asia, and the western Pacific. Hypolepis is tropical and south-temperate. Blotiella is strongly centered in Africa. Histiopteris is generally Malesian, with one pantropic to south-temperate species. [6] The extinct genus Krameropteris is known from remains found in Cenomanian aged Burmese amber. [7]

History of classification

Dennstaedtiaceae was previously considered the only family in the order Dennstaedtiales. Dennstaedtiaceae now contains the previously defined families Monachosoraceae Ching, Pteridiaceae Ching, and Hypolepidaceae Pic. Serm. [3] Before Smith's [3] classification in 2006, Dennstaedtiaceae was a poly- and para- phyletic family, [8] [9] [10] containing genera that now are classified within Lindsaeaceae and Saccolomataceae, and with the family Monachosoraceae arising from within the Dennstaedtiaceae clade. [3] The nonmonophyletic nature of Dennstaedtiaceae (pre-2006 classification) was proved and supported by multiple molecular studies. Dennstaedtiaceae as now classified is supported as monophyletic, but the relation of the genera within the family have not yet been fully clarified. [10]

Phylogeny of Dennstaedtiaceae [11] [12]

Monachosoroideae

Monachosorum Kunze 1848

Dennstaedtioideae
Microlepieae

Paradennstaedtia Tagawa 1952

Leptolepia Mettenius ex Kuhn

Oenotrichia Copeland 1929

Dennstaedtia Moore 1859 non Bernhardi 1801

Dennstaedtia species-group 2

Dennstaedtia species-group 3

Microlepia Presl 1836

Hypolepideae

Pteridium Gleditsch ex Scopoli 1760 nom. cons. non Rafinesque 1814

Paesia Saint-Hilaire 1833

Hiya Shang 2018

Histiopteris (Agardh 1839) Smith 1875

Blotiella Tryon 1962

Hypolepis Bernhardi 1805 non Palisot de Beauvois ex T. Lestib. 1819 non Nees 1829 non Pers. 1807

Interesting species within Dennstaedtiaceae

Dennsteadtiaceae species and genera are usually known for their weedy nature (i.e. Pteridium spp., Hypolepis spp., Paesia spp.), but some species are grown ornamentally (Blotiella spp., Dennstaedtia spp., Hypolepis spp., Microlepia spp.). [13]
The fiddleheads/crosiers of Pteridium aquilinum have been known to be eaten, but they contain carcinogens, so this practice is not prevalent. [14]
The rhizomes of Pteridium esculentum were consumed by the Maori during their settlement of New Zealand in the 13th century, but no longer are a part of the Maori diet. [5] The rhizomes of Pteridium esculentum contain about 50% starch when they grow in loose rich soil, at relatively deep depths. [5] The rhizomes were a staple in the diet because once dried, the rhizomes were very light (perfect for travelling) and would keep for about a year as long as they remained dry. [5] The leaves and spores of the Pteridium esculentum are associated with toxins and carcinogens, and have been known to cause stock (cattle, sheep, horses, pigs) to sicken. [5]

Related Research Articles

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The ferns are a group of vascular plants that reproduce via spores and have neither seeds nor flowers. They differ from mosses by being vascular, i.e., having specialized tissues that conduct water and nutrients, and in having life cycles in which the branched sporophyte is the dominant phase.

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

Thelypteridaceae is a family of about 900 species of ferns in the order Polypodiales. In the Pteridophyte Phylogeny Group classification of 2016, it is placed in the suborder Aspleniineae. Alternatively, the family may be submerged in a very broadly defined family Aspleniaceae as the subfamily Thelypteridoideae.

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

Ophioglossaceae, the adder's-tongue family, is a small family of ferns. In the Pteridophyte Phylogeny Group classification of 2016, it is the only family in the order Ophioglossales, which together with the Psilotales is placed in the subclass Ophioglossidae. The Ophioglossidae are one of the groups traditionally known as eusporangiate ferns. Members of the family differ from other ferns in a number of ways. Many have only a single fleshy leaf at a time. Their gametophytes are subterranean and rely on fungi for energy.

<i>Osmunda</i> Genus of ferns

Osmunda is a genus of primarily temperate-zone ferns of family Osmundaceae. Five to ten species have been listed for this genus.

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

Marattiaceae is the only family of extant (living) ferns in the order Marattiales. In the Pteridophyte Phylogeny Group classification of 2016, Marattiales is the only order in the subclass Marattiidae. The family has six genera and about 110 species. Many are different in appearance from other ferns, having large fronds and fleshy rootstocks.

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

The Dryopteridaceae are a family of leptosporangiate ferns in the order Polypodiales. They are known colloquially as the wood ferns. In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the family is placed in the suborder Polypodiineae. Alternatively, it may be treated as the subfamily Dryopteridoideae of a very broadly defined family Polypodiaceae sensu lato.

<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">Polypodiales</span> Order of ferns

The order Polypodiales encompasses the major lineages of polypod ferns, which comprise more than 80% of today's fern species. They are found in many parts of the world including tropical, semitropical and temperate areas.

<i>Oleandra</i> Genus of ferns

Oleandra is a genus of ferns. In the Pteridophyte Phylogeny Group classification of 2016, it is the only genus in the family Oleandraceae, which is placed in suborder Polypodiineae, order Polypodiales. Alternatively, the family may be placed in a very broadly defined family Polypodiaceae sensu lato as the subfamily Oleandroideae.

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

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<i>Pteridium aquilinum</i> Species of plant (fern)

Pteridium aquilinum, commonly called bracken, brake, pasture brake, common bracken, and also known as eagle fern, is a species of fern occurring in temperate and subtropical regions in both hemispheres. Originally native to Eurasia and North America, the extreme lightness of its spores has led to it achieving a cosmopolitan distribution.

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

Pteridaceae is a family of ferns in the order Polypodiales, including some 1150 known species in ca 45 genera, divided over five subfamilies. The family includes four groups of genera that are sometimes recognized as separate families: the adiantoid, cheilanthoid, pteridoid, and hemionitidoid ferns. Relationships among these groups remain unclear, and although some recent genetic analyses of the Pteridales suggest that neither the family Pteridaceae nor the major groups within it are all monophyletic, as yet these analyses are insufficiently comprehensive and robust to provide good support for a revision of the order at the family level.

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

The Athyriaceae are a family of terrestrial ferns in the order Polypodiales. In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the family is placed in the suborder Aspleniineae, and includes two genera. Alternatively, it may be treated as the subfamily Athyrioideae of a very broadly defined family Aspleniaceae. The family has with a cosmopolitan distribution.

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

The Lomariopsidaceae is a family of ferns with a largely tropical distribution. In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the family is placed in the suborder Polypodiineae of the order Polypodiales. Alternatively, it may be treated as the subfamily Lomariopsidoideae of a very broadly defined family Polypodiaceae sensu lato.

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

Lindsaeaceae is a pantropical family of ferns in the order Polypodiales. It contains six or seven genera with about 220 known species, some of which also extend into the more temperate regions of eastern Asia, New Zealand, and South America.

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

Saccolomataceae is a family of ferns in the order Polypodiales with about 19 species. It has been formerly treated as part of the Dennstaedtiaceae, however it has been classified as its own family according to Smith et al. (2006) The genus Saccoloma has been classified to include Orthiopteris, but the phylogeny of the group not yet fully understood. The family includes a dozen known species.

Lonchitis is a neotropical genus of ferns. It is the sole genus in the family Lonchitidaceae. At one time Lonchitis was placed in the Dennstaedtiaceae, and then transferred to the Lindsaeaceae, before being placed in its own family.

<i>Didymoglossum</i> Genus of ferns

Didymoglossum is a tropical genus of ferns in the family Hymenophyllaceae. It comprises more than 30 epilithic or low-epiphytic species under two subgenera. The genus is accepted in the Pteridophyte Phylogeny Group classification of 2016, but not by some other sources which sink it into a broadly defined Trichomanes.

<i>Haplopteris</i> Genus of ferns

Haplopteris is a genus of vittarioid ferns, a member of subfamily Vittarioideae and family Pteridaceae.

<i>Dennstaedtia christophelii</i> Fossil species of fern

Dennstaedtia christophelii is an extinct species of fern in the family Dennstaedtiaceae related to the modern hayscented ferns. The species is known from fossil fronds found in early Eocene sites of northern Washington state, United States and central British Columbia, Canada. The species is suggested to be closest to a Neotropical "Patania" clade and specifically the species Dennstaedtia producta and Dennstaedtia mathewsii.

References

  1. Dennstaedtiaceae Pic.Serm. Plants of the World Online . Retrieved 22 January 2024.
  2. Christenhusz, M. J. M.; Byng, J. W. (2016). "The number of known plants species in the world and its annual increase". Phytotaxa. 261 (3). Magnolia Press: 201–217. doi: 10.11646/phytotaxa.261.3.1 .
  3. 1 2 3 4 5 Smith, A. R., K. M. Pryer, et al. (2006). "A classification for extant ferns." Taxon 55(3): 705-731
  4. Thomson, J. (2000). "Morphological and Genomic Diversity in the Genus Pteridium (Dennstaedtiaceae)." Annals of Botany 85(Suppl B): 77-99
  5. 1 2 3 4 5 McGlone, M. S., J. M. Wilmshurst, et al. (2005). "An ecological and historical review of bracken(Pteridium esculentum) in New Zealand, and its cultural significance." New Zealand Journal of Ecology 29(2): 165-184
  6. Kramer, K. U. (1990). Dennstaedtiaceae. The Families and Genera of Vascular Plants: Pteridophytes and Gymnosperms. K. Kubitzki, K. U. Kramer and P. S. Green. New York, Springer-Verlag. 1: 81-94
  7. Schneider, Harald; Schmidt, Alexander R.; Heinrichs, Jochen (February 2016). "Burmese amber fossils bridge the gap in the Cretaceous record of polypod ferns". Perspectives in Plant Ecology, Evolution and Systematics. 18: 70–78. doi:10.1016/j.ppees.2016.01.003. hdl: 10141/610456 .
  8. Wolf, P. G. (1997). "Evaluation of atpB Nucleotide Sequences for Phylogenetic Studies of Ferns and Other Pteridophytes." American Journal of Botany 84(10): 1429-1440
  9. Hasebe, M., P. G. Wolf, et al. (1995). "Fern Phylogeny Based on rbcL Nucleotide Sequences." American Fern Journal 85(4): 134-181
  10. 1 2 Wolf, P. G. (1995). "Phylogenetic Analyses of rbcL and Nuclear Ribosomal RNA Gene Sequences in Dennstaedtiaceae." American Fern Journal 85(4): 306-327
  11. 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: 909768. doi: 10.3389/fpls.2022.909768 . PMC   9449725 . PMID   36092417.
  12. "Tree viewer: interactive visualization of FTOL". FTOL v1.4.0 [GenBank release 253]. 2023. Retrieved 8 March 2023.
  13. Mabberley, D. J. (1997). The Plant-Book, Cambridge University.
  14. Judd, W. S., C. C. Campbell, et al. (2008). Plant Systematics: A Phylogenetic Approach. Sunderland, Ma, Sinauer Associates, Inc.