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A pteridophyte is a (with and ) that reproduces by means of . Because pteridophytes produce neither nor , they are sometimes referred to as "", meaning that their means of reproduction is hidden. They are also the ancestors of the plants we see today.

, (often treated as ferns), and (, , and ) are all pteridophytes. However, they do not form a monophyletic group because ferns (and horsetails) are more closely related to than to lycophytes. "Pteridophyta" is thus no longer a widely accepted taxon, but the term pteridophyte remains in common parlance, as do pteridology and pteridologist as a science and its practitioner, for example by the International Association of Pteridologists and the Pteridophyte Phylogeny Group.


Etymology
The name Pteridophyte is a compound word created by English speakers around 1880. It is formed from the prefix pterido- meaning fern, a Latin borrowing of the Greek word pterís which derives from pterón meaning feather. The suffix, -phyte, is a suffix meaning plant from the ancient Greek word phyton (φυτόν).


Description
Pteridophytes (ferns and lycophytes) are free-sporing that have a life cycle with alternating, free-living and phases that are independent at maturity. The body of the sporophyte is well differentiated into roots, stem and leaves. The root system is always . The stem is either underground or aerial. The leaves may be microphylls or megaphylls. Their other common characteristics include vascular plant (e.g., ) and (e.g., dispersal and the absence of ).


Taxonomy

Phylogeny
Of the pteridophytes, ferns account for nearly 90% of the extant diversity. Smith et al. (2006), the first higher-level pteridophyte classification published in the molecular phylogenetic era, considered the ferns as monilophytes, as follows:

where the monilophytes comprise about 9,000 species, including (), (Psilotaceae), and all eusporangiate and all leptosporangiate ferns. Historically both lycophytes and monilophytes were grouped together as pteridophytes (ferns and fern allies) on the basis of being spore-bearing ("seed-free"). In Smith's molecular phylogenetic study the ferns are characterised by origin in the , usually in shoots, a pseudoendospore, tapetum, and with 30-1000 . The term "moniliform" as in Moniliformopses and monilophytes means "bead-shaped" and was introduced by Kenrick and Crane (1997) as a scientific replacement for "fern" (including Equisetaceae) and became established by Pryer et al. (2004). Christenhusz and Chase (2014) in their review of classification schemes provide a critique of this usage, which they discouraged as irrational. In fact the alternative name was already in use. By comparison "lycopod" or lycophyte (club moss) means wolf-plant. The term "" included under Pteridophyta generally refers to vascular spore-bearing plants that are not ferns, including lycopods, horsetails, whisk ferns and water ferns (, and ). This is not a natural grouping but rather a convenient term for non-fern, and is also discouraged, as is eusporangiate for non-leptosporangiate ferns.

However both Infradivision and Moniliformopses are also invalid names under the International Code of Botanical Nomenclature. Ferns, despite forming a , are formally only considered as four classes (; ; ; ), 11 orders and 37 families, without assigning a higher .

Furthermore, within the Polypodiopsida, the largest grouping, a number of informal clades were recognised, including leptosporangiates, core leptosporangiates, (Polypodiales), and eupolypods (including and ).

In 2014 Christenhusz and Chase, summarising the known knowledge at that time, treated this group as two separate unrelated taxa in a consensus classification;

  • (lycopods) 1 subclass, 3 orders, each with one family, 5 genera, approx. 1,300 species
  • (ferns) 4 subclasses, 11 orders, 21 families, approx. 212 genera, approx. 10,535 species
These subclasses correspond to Smith's four classes, with Ophioglossidae corresponding to Psilotopsida.

The two major groups previously included in Pteridophyta are related as follows:


Subdivision
Pteridophytes consist of two separate but related classes, whose nomenclature has varied. The system put forward by the Pteridophyte Phylogeny Group in 2016, PPG I, is:
  • Class Bartl. – lycophytes: clubmosses, quillworts and spikemosses; 3 extant orders
:*Order DC. ex Bercht. & J.Presl – clubmosses; 1 extant family
:*Order Prantl – quillworts; 1 extant family
:*Order Prantl – spikemosses; 1 extant family

In addition to these living groups, several groups of pteridophytes are now and known only from . These groups include the , Zosterophyllopsida, Trimerophytopsida, the and the Progymnospermopsida.

Modern studies of the land plants agree that seed plants emerged from . Therefore, pteridophytes do not form a clade but constitute a grade.


Life cycle
Just as with and (seed plants), the life cycle of pteridophytes involves alternation of generations. This means that a generation (the sporophyte, which produces spores) is followed by a generation (the gametophyte or , which produces ). Pteridophytes differ from bryophytes in that the sporophyte is branched and generally much larger and more conspicuous, and from seed plants in that both generations are independent and free-living. The sexuality of pteridophyte gametophytes can be classified as follows:
  • : each individual gametophyte is either male (producing and hence ) or female (producing and hence ).
  • : each individual gametophyte produces both antheridia and archegonia and can function both as a male and as a female.
  • : : the antheridia mature before the archegonia (male first, then female).
  • : : the archegonia mature before the antheridia (female first, then male).

These terms are not the same as and , which refer to whether a seed plant's sporophyte bears both male and female gametophytes, i.e., produces both pollen and seeds, or just one.


See also


Bibliography


External links

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