Lycopodiopsida

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Lycopodiopsida
Temporal range: Devonian–Recent
Lycopodium plant.jpg
Palhinhaea cernua with close-up of branch
Scientific classification OOjs UI icon edit-ltr.svg
Kingdom: Plantae
Clade: Tracheophytes
Clade: Lycophytes
Class: Lycopodiopsida
Bartl.
Orders
Synonyms

See Table 1.

Lycopodiopsida is a class of vascular plants also known as lycopods or lycophytes. Members of the class are also called clubmosses, firmosses, spikemosses and quillworts. They have dichotomously branching stems bearing simple leaves called microphylls and reproduce by means of spores borne in sporangia on the sides of the stems at the bases of the leaves. Although living species are small, during the Carboniferous, extinct tree-like forms (Lepidodendrales) formed huge forests that dominated the landscape and contributed to coal deposits.

Contents

The nomenclature and classification of plants with microphylls varies substantially among authors. A consensus classification for extant (living) species was produced in 2016 by the Pteridophyte Phylogeny Group (PPG I), which places them all in the class Lycopodiopsida, which includes the classes Isoetopsida and Selaginellopsida used in other systems. (See Table 2.) Alternative classification systems have used ranks from division (phylum) to subclass. In the PPG I system, the class is divided into three orders, Lycopodiales, Isoetales and Selaginellales.

Characteristics

Club-mosses (Lycopodiales) are homosporous, but the genera Selaginella (spikemosses) and Isoetes (quillworts) are heterosporous, with female spores larger than the male. [1] As a result of fertilisation, the female gametophyte produces sporophytes. A few species of Selaginella such as S. apoda and S. rupestris are also viviparous; the gametophyte develops on the mother plant, and only when the sporophyte's primary shoot and root is developed enough for independence is the new plant dropped to the ground. [2] Many club-moss gametophytes are mycoheterotrophic and long-lived, residing underground for several years before emerging from the ground and progressing to the sporophyte stage. [3]

Lycopodiaceae and spikemosses (Selaginella) are the only vascular plants with biflagellate sperm, an ancestral trait in land plants otherwise only seen in bryophytes. The only exceptions are Isoetes and Phylloglossum, which independently has evolved multiflagellated sperm cells with approximately 20 flagella [4] [5] (sperm flagella in other vascular plants can count at least thousand, but is completely absent in seed plants except for Ginkgo and cycads). [6] Because only two flagella puts a size limit on the genome, we find the largest known genomes in the clade in Isoetes, as multiflagellated sperm is not exposed for the same selection pressure as biflagellate sperm in regard of size. [7]

Taxonomy

Phylogeny

The extant lycophytes are vascular plants (tracheophytes) with microphyllous leaves, distinguishing them from the euphyllophytes (plants with megaphyllous leaves). The sister group of the extant lycophytes and their closest extinct relatives are generally believed to be the zosterophylls, a paraphyletic or plesion group. Ignoring some smaller extinct taxa, the evolutionary relationships are as shown below. [8] [9] [10]

tracheophytes
lycophytes
zosterophylls

(multiple branches, incertae sedis )

 lycopodiopsida 

living lycophytes and
their extinct close relatives

(broadly defined)
euphyllophytes

ferns & horsetails

spermatophytes
(seed plants)

(vascular plants)

As of 2019, there was broad agreement, supported by both molecular and morphological evidence, that the extant lycophytes fell into three groups, treated as orders in PPG I, and that these, both together and individually, are monophyletic, being related as shown in the cladogram below: [10]

extant lycophytes

Classification

The rank and name used for the taxon holding the extant lycophytes (and their closest extinct relatives) varies widely. Table 1 below shows some of the highest ranks that have been used. Systems may use taxa at a rank lower than the highest given in the table with the same circumscription; for example, a system that uses Lycopodiophyta as the highest ranked taxon may place all of its members in a single subclass.

Table 1: Alternative highest ranks used which include only extant species and their closest relatives
Highest rankNameExample sources
Division (phylum)LycophytaTaylor et al. (2009), [11] Mauseth (2014) [9]
Division (phylum)LycopodiophytaNiklas (2016) [12]
Subdivision (subphylum)LycopodiophytinaRuggiero et al. (2015) [13]
ClassLycopsidaKenrick & Crane (1997) [8] [14]
ClassLycopodiopsidaPPG I (2016) [10]
SubclassLycopodiidaeChase & Reveal (2009) [15]

Some systems use a higher rank for a more broadly defined taxon of lycophytes that includes some extinct groups more distantly related to extant lycophytes, such as the zosterophylls. For example, Kenrick & Crane (1997) use the subdivision Lycophytina for this purpose, with all extant lycophytes falling within the class Lycopsida. [8] Other sources exclude the zosterophylls from any "lycophyte" taxon. [11]

In the Pteridophyte Phylogeny Group classification of 2016 (PPG I), the three orders are placed in a single class, Lycopodiopsida, holding all extant lycophyte species. Older systems have used either three classes, one for each order, or two classes, recognizing the closer relationship between Isoetales and Selaginellales. In these cases, a higher ranked taxon is needed to contain the classes (see Table 1). As Table 2 shows, the names "Lycopodiopsida" and "Isoetopsida" are both ambiguous.

Table 2: Alternative arrangements of the orders of extant lycophytes into classes
Order3 classes
e.g. IUCN Red List, 2004 [16]
2 classes
e.g. Yatsentyuk et al. (2001) [17]
1 class
PPG I [10]
LycopodialesLycopodiopsidaLycopodiopsidaLycopodiopsida
IsoetalesIsoetopsidaIsoetopsida
SelaginellalesSellaginellopsida

Subdivisions

The PPG I system divides up the extant lycophytes as shown below.

  • Order Lycopodiales DC. ex Bercht. & J.Presl (1 extant family)

Some extinct groups, such as zosterophylls, fall outside the limits of the taxon as defined by the classifications in Table 1 above. However, other extinct groups fall within some circumscriptions of this taxon. Taylor et al. (2009) and Mauseth (2014) include a number of extinct orders in their division (phylum) Lycophyta, although they differ on the placement of some genera. [11] [9] The orders included by Taylor et al. are: [11]

Mauseth uses the order †Asteroxylales, placing Baragwanathia in the Protolepidodendrales. [9]

The relationship between some of these extinct groups and the extant ones was investigated by Kenrick and Crane in 1997. When the genera they used are assigned to orders, their suggested relationship is: [18]

†Drepanophycales († Asteroxylon , † Baragwanathia , † Drepanophycus )

Lycopodiales

†Protolepidodendrales († Leclercqia , † Minarodendron )

Selaginellales ( Selaginella , including subg. Stachygynandrum and subg. Tetragonostachys)

Isoetales ( Isoetes )

†Lepidodendrales († Paralycopodites )

Evolution

Artist's impression of a Lepidodendron Lepidodendron.png
Artist's impression of a Lepidodendron
External impression of Lepidodendron from the Upper Carboniferous of Ohio LepidodendronOhio.jpg
External impression of Lepidodendron from the Upper Carboniferous of Ohio
Axis (branch) from Archaeosigillaria or related lycopod from the Middle Devonian of Wisconsin Lycopod axis.jpg
Axis (branch) from Archaeosigillaria or related lycopod from the Middle Devonian of Wisconsin

The Lycopodiopsida are distinguished from other vascular plants by the possession of microphylls and by their sporangia, which are lateral as opposed to terminal and which open (dehisce) transversely rather than longitudinally. In some groups, the sporangia are borne on sporophylls that are clustered into strobili. Phylogenetic analysis shows the group branching off at the base of the evolution of vascular plants and they have a long evolutionary history. Fossils are abundant worldwide, especially in coal deposits. Fossils that can be ascribed to the Lycopodiopsida first appear in the Silurian period, along with a number of other vascular plants. The Silurian Baragwanathia longifolia is one of the earliest identifiable species. Lycopodolica is another Silurian genus which appears to be an early member of this group. [19] The group evolved roots independently from the rest of the vascular plants. [20] [21]

From the Devonian onwards, some species grew large and tree-like. Devonian fossil lycopsids from Svalbard, growing in equatorial regions, raise the possibility that they drew down enough carbon dioxide to change the Earth's climate significantly. [22] During the Carboniferous, tree-like plants (such as Lepidodendron , Sigillaria , and other extinct genera of the order Lepidodendrales) formed huge forests that dominated the landscape. Unlike modern trees, leaves grew out of the entire surface of the trunk and branches, but fell off as the plant grew, leaving only a small cluster of leaves at the top. The lycopsids had distinctive features such as Lepidodendron lycophytes, which were marked with diamond-shaped scars where they once had leaves. Quillworts (order Isoetales) and Selaginella are considered their closest extant relatives and share some unusual features with these fossil lycopods, including the development of both bark, cambium and wood, a modified shoot system acting as roots, bipolar and secondary growth, and an upright stance. [2] [23] The remains of Lepidodendron lycopods formed many fossil coal deposits. In Fossil Grove, Victoria Park, Glasgow, Scotland, fossilized lycophytes can be found in sandstone.

The Lycopodiopsida had their maximum diversity in the Pennsylvanian (Upper Carboniferous), particularly tree-like Lepidodendron and Sigillaria that dominated tropical wetlands. The complex ecology of these tropical rainforests collapsed during the Middle Pennsylvanian due to a change in climate. [24] In Euramerica, tree-like species apparently became extinct in the Late Pennsylvanian, as a result of a transition to a much drier climate, giving way to conifers, ferns and horsetails. In Cathaysia (now South China), tree-like species survived into the Permian. Nevertheless, lycopodiopsids are rare in the Lopingian (latest Permian), but regained dominance in the Induan (earliest Triassic), particularly Pleuromeia . After the worldwide Permian–Triassic extinction event, members of this group pioneered the repopulation of habitats as opportunistic plants. The heterogeneity of the terrestrial plant communities increased markedly during the Middle Triassic when plant groups like horsetails, ferns, pteridosperms, cycads, ginkgos and conifers resurfaced and diversified quickly. [25]

Microbial associations

Lycophytes form associations with microbes such as fungi and bacteria, including arbuscular mycorrhizal and endophytic associations.

Arbuscular mycorrhizal associations have been characterized in all stages of the lycophyte lifecycle: mycoheterotrophic gametophyte, photosynthetic surface-dwelling gametophyte, young sporophyte, and mature sporophyte. [3] Arbuscular mycorrhizae have been found in Selaginella spp. roots and vesicles. [26]

During the mycoheterotrophic gametophyte lifecycle stage, lycophytes gain all of their carbon from subterranean glomalean fungi. In other plant taxa, glomalean networks transfer carbon from neighboring plants to mycoheterotrophic gametophytes. Something similar could be occurring in Huperzia hypogeae gametophytes which associate with the same glomalean phenotypes as nearby Huperzia hypogeae sporophytes. [3]

Fungal endophytes have been found in many species of lycophyte, however the function of these endophytes in host plant biology is not known. Endophytes of other plant taxa perform roles such as improving plant competitive fitness, conferring biotic and abiotic stress tolerance, promoting plant growth through phytohormone production or production of limiting nutrients. [27] However, some endophytic fungi in lycophytes do produce medically relevant compounds. Shiraia sp Slf14 is an endophytic fungus present in Huperzia serrata that produces Huperzine A, a biomedical compound which has been approved as a drug in China and a dietary supplement in the U.S. to treat Alzheimer's Disease. [28] This fungal endophyte can be cultivated much more easily and on a much larger scale than H. serrata itself which could increase the availability of Huperzine A as a medicine.

Uses

The spores of lycopods are highly flammable and so have been used in fireworks. [29] Lycopodium powder, the dried spores of the common clubmoss, was used in Victorian theater to produce flame-effects. A blown cloud of spores burned rapidly and brightly, but with little heat. (It was considered safe by the standards of the time.)[ citation needed ]

Related Research Articles

<span class="mw-page-title-main">Gametophyte</span> Haploid stage in the life cycle of plants and algae

A gametophyte is one of the two alternating multicellular phases in the life cycles of plants and algae. It is a haploid multicellular organism that develops from a haploid spore that has one set of chromosomes. The gametophyte is the sexual phase in the life cycle of plants and algae. It develops sex organs that produce gametes, haploid sex cells that participate in fertilization to form a diploid zygote which has a double set of chromosomes. Cell division of the zygote results in a new diploid multicellular organism, the second stage in the life cycle known as the sporophyte. The sporophyte can produce haploid spores by meiosis that on germination produce a new generation of gametophytes.

<span class="mw-page-title-main">Fern</span> Class of vascular plants

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.

<i>Selaginella</i> Genus of vascular plants in the family Selaginellaceae

Selaginella is the sole genus in the family Selaginellaceae, the spikemosses or lesser clubmosses, a kind of vascular plant.

<i>Isoetes</i> Genus of vascular plants in the family Isoetaceae

Isoetes, commonly known as the quillworts, is a genus of lycopod. It is the only living genus in the family Isoetaceae and order Isoetales. There are currently 192 recognized species, with a cosmopolitan distribution mostly in aquatic habitats but with the individual species often scarce to rare. Some botanists split the genus, separating two South American species into the genus Stylites, although molecular data place these species among other species of Isoetes, so that Stylites does not warrant taxonomic recognition. Species virtually identical to modern quillworts have existed since the Jurassic epoch, though the timing of the origin of modern Isoetes is subject to considerable uncertainty.

<span class="mw-page-title-main">Lycophyte</span> Broadly circumscribed group of spore bearing plants

The lycophytes, when broadly circumscribed, are a group of vascular plants that include the clubmosses. They are sometimes placed in a division Lycopodiophyta or Lycophyta or in a subdivision Lycopodiophytina. They are one of the oldest lineages of extant (living) vascular plants; the group contains extinct plants that have been dated from the Silurian. Lycophytes were some of the dominating plant species of the Carboniferous period, and included the tree-like Lepidodendrales, some of which grew over 40 metres (130 ft) in height, although extant lycophytes are relatively small plants.

<span class="mw-page-title-main">Lycopodiaceae</span> Family of vascular plants

The Lycopodiaceae are an old family of vascular plants, including all of the core clubmosses and firmosses, comprising 16 accepted genera and about 400 known species. This family originated about 380 million years ago in the early Devonian, though the diversity within the family has been much more recent. "Wolf foot" is another common name for this family due to the resemblance of either the roots or branch tips to a wolf's paw.

<span class="mw-page-title-main">Bryophyte</span> Terrestrial plants that lack vascular tissue

Bryophytes are a group of land plants, sometimes treated as a taxonomic division, that contains three groups of non-vascular land plants (embryophytes): the liverworts, hornworts, and mosses. In the strict sense, Bryophyta consists of the mosses only. Bryophytes are characteristically limited in size and prefer moist habitats although they can survive in drier environments. The bryophytes consist of about 20,000 plant species. Bryophytes produce enclosed reproductive structures, but they do not produce flowers or seeds. They reproduce sexually by spores and asexually by fragmentation or the production of gemmae. Though bryophytes were considered a paraphyletic group in recent years, almost all of the most recent phylogenetic evidence supports the monophyly of this group, as originally classified by Wilhelm Schimper in 1879. The term bryophyte comes from Ancient Greek βρύον (brúon) 'tree moss, liverwort', and φυτόν (phutón) 'plant'.

<span class="mw-page-title-main">Embryophyte</span> Subclade of green plants, also known as land plants

The embryophytes are a clade of plants, also known as Embryophyta or land plants. They are the most familiar group of photoautotrophs that make up the vegetation on Earth's dry lands and wetlands. Embryophytes have a common ancestor with green algae, having emerged within the Phragmoplastophyta clade of freshwater charophyte green algae as a sister taxon of Charophyceae, Coleochaetophyceae and Zygnematophyceae. Embryophytes consist of the bryophytes and the polysporangiophytes. Living embryophytes include hornworts, liverworts, mosses, lycophytes, ferns, gymnosperms and angiosperms. Embryophytes have diplobiontic life cycles.

<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>Lepidodendron</i> Extinct genus of vascular plants of the Carboniferous to Triassic

Lepidodendron is an extinct genus of primitive lycopodian vascular plants belonging the order Lepidodendrales. It is well preserved and common in the fossil record. Like other Lepidodendrales, species of Lepidodendron grew as large-tree-like plants in wetland coal forest environments. They sometimes reached heights of 50 metres, and the trunks were often over 1 m (3.3 ft) in diameter. They are often known as "scale trees", due to their bark having been covered in diamond shaped leaf-bases, from which leaves grew during earlier stages of growth. However, they are correctly defined as arborescent lycophytes. They thrived during the Carboniferous Period, and persisted until the end of the Permian around 252 million years ago. Sometimes erroneously called "giant club mosses", the genus was actually more closely related to modern quillworts than to modern club mosses. In the form classification system used in paleobotany, Lepidodendron is both used for the whole plant as well as specifically the stems and leaves.

<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.

<i>Lycopodiella</i> Genus of spore-bearing plants

Lycopodiella is a genus in the clubmoss family Lycopodiaceae. The genus members are commonly called bog clubmosses, describing their wetland habitat. The genus has a cosmopolitan distribution, with centers of diversity in the tropical New World and New Guinea. In the past, the genus was often incorporated within the related genus Lycopodium, but was segregated in 1964. In the Pteridophyte Phylogeny Group classification of 2016, Lycopodiella is placed in the subfamily Lycopodielloideae, along with three other genera. In this circumscription, the genus has about 15 species. Other sources use a wider circumscription, in which the genus is equivalent to the Lycopodielloideae of PPG I, in which case about 40 species and hybrids are accepted.

<i>Cooksonia</i> Group of vascular land plants (extinct)

Cooksonia is an extinct group of primitive land plants, treated as a genus, although probably not monophyletic. The earliest Cooksonia date from the middle of the Silurian ; the group continued to be an important component of the flora until the end of the Early Devonian, a total time span of 433 to 393 million years ago. While Cooksonia fossils are distributed globally, most type specimens come from Britain, where they were first discovered in 1937. Cooksonia includes the oldest known plant to have a stem with vascular tissue and is thus a transitional form between the primitive non-vascular bryophytes and the vascular plants.

<span class="mw-page-title-main">Zosterophyll</span> Group of extinct land plants that first appeared in the Silurian period

The zosterophylls are a group of extinct land plants that first appeared in the Silurian period. The taxon was first established by Banks in 1968 as the subdivision Zosterophyllophytina; they have since also been treated as the division Zosterophyllophyta or Zosterophyta and the class or plesion Zosterophyllopsida or Zosteropsida. They were among the first vascular plants in the fossil record, and had a world-wide distribution. They were probably stem-group lycophytes, forming a sister group to the ancestors of the living lycophytes. By the late Silurian a diverse assemblage of species existed, examples of which have been found fossilised in what is now Bathurst Island in Arctic Canada.

<i>Selaginella moellendorffii</i> Species of spore-bearing plant

Selaginella moellendorffii is a lycophyte that is an important model organism, especially in comparative genomics. S. moellendorffii is a member of an ancient vascular plant lineage that first appeared in the fossil record some 400 million years ago. They would later form a dominant part of the world's flora during the Carboniferous period. They have a number of unusual and/or "primitive" features, such as rudimentary leaves (microphylls), ubiquitous dichotomous branching, heterospory, and the ligule. As the earliest diverging group of modern vascular plants, they are essential to understanding the evolution of plants as a whole.

<span class="mw-page-title-main">Polysporangiophyte</span> Spore-bearing plants with branched sporophytes

Polysporangiophytes, also called polysporangiates or formally Polysporangiophyta, are plants in which the spore-bearing generation (sporophyte) has branching stems (axes) that bear sporangia. The name literally means 'many sporangia plant'. The clade includes all land plants (embryophytes) except for the bryophytes whose sporophytes are normally unbranched, even if a few exceptional cases occur. While the definition is independent of the presence of vascular tissue, all living polysporangiophytes also have vascular tissue, i.e., are vascular plants or tracheophytes. Extinct polysporangiophytes are known that have no vascular tissue and so are not tracheophytes.

<i>Horneophyton</i> Extinct genus of early plants

Horneophyton is an extinct early plant which may form a "missing link" between the hornworts and the Rhyniopsida. It is a member of the class Horneophytopsida. Horneophyton is among the most abundant fossil organisms found in the Rhynie chert, a Devonian Lagerstätte in Aberdeenshire, UK. A single species, Horneophyton lignieri, is known. Its probable female gametophyte is the form taxon Langiophyton mackiei.

<span class="mw-page-title-main">Lepidodendrales</span> Extinct order of vascular tree-like plants

Lepidodendrales or arborescent lycophytes are an extinct order of primitive, vascular, heterosporous, arborescent (tree-like) plants belonging to Lycopodiopsida. Members of Lepidodendrales are the best understood of the fossil lycopsids due to the vast diversity of Lepidodendrales specimens and the diversity in which they were preserved; the extensive distribution of Lepidodendrales specimens as well as their well-preservedness lends paleobotanists exceptionally detailed knowledge of the coal-swamp giants’ reproductive biology, vegetative development, and role in their paleoecosystem. The defining characteristics of the Lepidodendrales are their secondary xylem, extensive periderm development, three-zoned cortex, rootlike appendages known as stigmarian rootlets arranged in a spiralling pattern, and megasporangium each containing a single functional megaspore that germinates inside the sporangium. Many of these different plant organs have been assigned both generic and specific names as relatively few have been found organically attached to each other. Some specimens have been discovered which indicate heights of 40 and even 50 meters and diameters of over 2 meters at the base. The massive trunks of some species branched profusely, producing large crowns of leafy twigs; though some leaves were up to 1 meter long, most were much shorter, and when leaves dropped from branches their conspicuous leaf bases remained on the surface of branches. Strobili could be found at the tips of distal branches or in an area at the top of the main trunk. The underground organs of Lepidodendrales typically consisted of dichotomizing axes bearing helically arranged, lateral appendages serving an equivalent function to roots. Sometimes called "giant club mosses", they are believed to be more closely related to extant quillworts based on xylem, although fossil specimens of extinct Selaginellales from the Late Carboniferous also had secondary xylem.

Hicklingia is a genus of extinct plants of the Middle Devonian. Compressed specimens were first described in 1923 from the Old Red Sandstone of Scotland. Initially the genus was placed in the "rhyniophytes", but this group is defined as having terminal sporangia, and later work showed that the sporangia of Hicklingia were lateral rather than strictly terminal, so that it is now regarded as having affinities with the zosterophylls.

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