Cooksonia
Cooksonia is an extinct grouping of primitive land plants. The earliest Cooksonia date from the middle of the Silurian (the Wenlock epoch);[1] 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.[4] 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.[5]
| Cooksonia | |
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| A cartoon of Cooksonia, reconstructed with non-photosynthetic axes, dependent on its gametophyte, as per Boyce (2008) | |
Scientific classification  | |
| Kingdom: | Plantae |
| Clade: | Tracheophytes |
| Stem group: | †Rhyniophytes |
| Form taxon: | †Cooksonioidea |
| Genus: | †Cooksonia Lang 1937 emend. Gonez & Gerrienne 2010[3] non Druce 1905 |
| Species | |
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Description
Only the sporophyte phase of Cooksonia is currently known (i.e. the phase which produces spores rather than gametes). Individuals were small, a few centimetres tall, and had a simple structure. They lacked leaves, flowers and roots—although it has been speculated that they grew from a rhizome that has not been preserved.[2] They had a simple stalk that branched dichotomously a few times. Each branch ended in a sporangium or spore-bearing capsule. In his original description of the genus, Lang described the sporangia as flattened, "with terminal sporangia that are short and wide", and in the species Cooksonia pertoni "considerably wider than high".[4] A 2010 review of the genus by Gonez and Gerrienne produced a tighter definition, which requires the sporangia to be more-or-less trumpet-shaped (as in the illustration), with a 'lid' or operculum which disintegrates to release the spores.[3]
Specimens of one species of Cooksonia have a dark stripe in the centre of their stalks, which has been interpreted as the earliest remains of water-carrying tissue.[6] Other Cooksonia species lacked such conducting tissue.
Cooksonia specimens occur in a range of sizes, and vary in stem width from about 0.03 mm to 3 mm. Specimens of different sizes were probably different species, not fragments of larger organisms: fossils occur in consistent size groupings, and sporangia and spore details are different in organisms of different sizes. The organisms probably exhibited determinate growth (i.e. stems did not grow further after producing sporangia).[2]
Some Cooksonia species bore stomata, which had a role in gas exchange; this was probably to assist in transpiration-driven transport of dissolved materials in the xylem, rather than primarily in photosynthesis, as suggested by their concentration at the tips of the axes. These clusterings of stomata are typically associated with a bulging in the axis at the neck of the sporangium, which may have contained photosynthetic tissue, reminiscent of some mosses.[2]
As the genus is circumscribed by Gonez and Gerrienne, there are six possible species. C. pertoni,[Note 1] C. paranensis and C. banksii are all relatively similar with flat-topped, trumpet-shaped sporangia; stems are somewhat narrower in C. paranensis than in C. pertoni. Only one specimen of C. bohemica is known. It has stouter, more branched stems; the original shape of the sporangia is unclear because of poor preservation. C. hemisphaerica, described from the same locality as C. pertoni, differs in having sporangia of which the tops, at least as preserved, are hemispherical rather than flat. C. cambrensis also has spherical sporangia, but without the gradual widening at the base characteristic of the other species. Preservation of the sporangia is again poor.[3] C. barrandei was described in 2018.[7]
Physiology
While reconstructions traditionally depict Cooksonia as a green and red, photosynthesising, self-sufficient stem, it is likely that at least some fossils instead preserve a sporophyte generation which was dependent on a gametophyte for its nutrition – a relationship that occurs in modern mosses and liverworts. However, no fossil evidence of a gametophyte of Cooksonia has been discovered to date.[2]
The widths of Cooksonia fossils span an order of magnitude. Study of smaller Cooksonia fossils showed that once the tissue required to support the axes, protect them from desiccation, and transport water had been accounted for, no room remained for photosynthetic tissue, and the sporophyte may therefore have been dependent on the gametophyte. Further, the axis thickness is what would be expected if its sole role was to support a sporangium. It appears that, originally at least, the role of the axes in smaller species was solely to ensure continued spore dispersal, even if the axis desiccated. The potential self-sufficiency of the larger axes may represent the evolution of an independent sporophyte generation.[2]
In 2018, the sporophyte of a new species, Cooksonia barrandei, was described, from about 432 million years ago. It is the oldest-known megafossil of land plants, as of May 2018. It was sufficiently robust to pass Boyce's test for possible self-sufficiency. Together with evidence that, unlike modern mosses and liverworts, hornwort sporophytes do have a degree of nutritional independence through photosynthesis, C. barrandei suggests that independent gametophyte and sporophyte generations could have been ancestral in land plants, rather than evolving later.[7]
Taxonomy
The first Cooksonia species were described by William Henry Lang in 1937 and named in honor of Isabel Cookson, with whom he had collaborated and who collected specimens of Cooksonia pertoni in Perton Quarry, Wales, in 1934.[4] There were originally two species, Cooksonia pertoni and C. hemisphaerica.[4] The genus was defined as having narrow leafless stems (axes), which branched dichotomously, with terminal sporangia that were "short and wide". There was a central vascular cylinder consisting of annular tracheids (water-conducting cells with thickened walls). Six other species were later added to the genus: C. crassiparietilis, C. caledonica, C. cambrensis, C. bohemica, C. paranensis and C. banksii. A review in 2010 concluded that the delineation of the genus was inaccurate and that some species needed to be removed; in particular those in which sporangia were not more-or-less trumpet-shaped. As amended by Gonez and Gerrienne, Cooksonia has the following species:
- Cooksonia pertoni – the type species designated by Gonez & Gerrienne
- Cooksonia paranensis
Five further species are considered doubtful because of the poor preservation of the specimens, but are left in the genus:
- Cooksonia acuminata
- Cooksonia bohemica
- Cooksonia cambrensis
- Cooksonia downtonensis
- Cooksonia rusanovii
Four species are excluded from the genus by Gonez and Gerrienne. Species that have been transferred or removed are:
- C. hemisphaerica Lang 1937
- C. crassiparietilis Yurina 1964
- C. caledonica Edwards 1970 now Aberlemnia caledonica (Edwards,, 1970) Gonez & Gerrienne, 2010[8]
- C. banksii Habgood et al. 2002 now Concavatheca banksii (Habgood, Edwards & Axe 2002) Morris et al. 2012b
C. caledonica and the less well-preserved C. crassiparietilis have sporangia which are composed of two 'valves', splitting to release their spores along a line opposite to where they are attached to the stem (i.e. distally).[3]
C. barrandei was described in 2018.[7]
Phylogeny
For some years, it was suspected that Cooksonia and its species were poorly characterized. Thus four different kinds of spore, probably representing four different species, were found in sporangia originally identified as C. pertoni.[9]
A 2010 study of the genus produced the consensus cladogram shown below (some branches have been collapsed to reduce the size of the diagram). This was based on data from an earlier study (by Kenrick and Crane[10]), supplemented by further information on Cooksonia species resulting from the authors' own research.[3]
| polysporangiophytes |
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This confirms that the genus Cooksonia sensu Lang (1937) is polyphyletic. A core group of five species are placed together, unresolved between the euphyllophytes and the lycophytes. The poorly preserved C. hemisphaerica is placed as the most basal tracheophyte. Two other species, C. crassiparietilis and C. caledonica, are placed in the stem group of the lycophytes. These two species have been removed from Cooksonia sensu Gonez & Gerrienne (C. caledonica has since been placed in a new genus Aberlemnia[8]). Both have sporangia which, although borne terminally rather than laterally, have a mechanism for releasing spores similar to those of the zosterophylls.[3]
A second cladistic analysis was carried out using only the three best preserved and thus best known species, C. pertoni, C. paranensis, and C. caledonica. The position of C. caledonica was confirmed, but C. pertoni and C. paranensis now formed a single clade more clearly related to the lycophytes than the euphyllophytes.[3]
Cooksonioids
Cooksonia and similar genera have been placed in a group called "cooksonioids". Originally the term was used for a group of plants fitting the general description of Cooksonia (i.e. simple plants with naked axes showing dichotomous branching and terminal sporangia), but with uncertain evidence of vascular tissue.[11] Boyce restricted the group to forms with axes usually less than 1 mm in diameter, and hence possibly not capable of independent growth. In addition to Cooksonia, he included genera such as Salopella, Tarrantia and Tortilicaulis.[2] Hue and Xao regarded cooksonioids as a group within the rhyniophytes with radially symmetrical sporangia of roughly the same height and width, and included Cooksonia pertoni, C. paranensis and C. hemisphaerica, but not C. crassiparietilis and Aberlemnia caledonica, as they had bilaterally symmetrical sporangia.[12]
Notes
- Two spellings are in use: the spelling used by the original author of the name, C. pertoni, and the spelling C. pertonii (e.g. in Bateman, R.M.; Crane, P.R.; Dimichele, W.A.; Kenrick, P.R.; Rowe, N.P.; Speck, T.; Stein, W.E. (1998), "Early Evolution of Land Plants: Phylogeny, Physiology, and Ecology of the Primary Terrestrial Radiation", Annual Review of Ecology and Systematics, 29 (1): 263–92, doi:10.1146/annurev.ecolsys.29.1.263). The second is appropriate in botanical Latin when an epithet relates to a person, according to Article 60.11 of the International Code of Nomenclature for algae, fungi, and plants.
References
- Edwards, D. & Feehan, J. (1980), "Records of Cooksonia-type sporangia from late Wenlock strata in Ireland", Nature, 287 (5777): 41–42, Bibcode:1980Natur.287...41E, doi:10.1038/287041a0, S2CID 7958927
- Boyce, C. Kevin (2008), "How green was Cooksonia? The importance of size in understanding the early evolution of physiology in the vascular plant lineage", Paleobiology, 34 (2): 179–194, doi:10.1666/0094-8373(2008)034[0179:HGWCTI]2.0.CO;2
- Gonez, P. & Gerrienne, P. (2010a), "A New Definition and a Lectotypification of the Genus Cooksonia Lang 1937", International Journal of Plant Sciences, 171 (2): 199–215, doi:10.1086/648988
- Lang, W.H. (1937), "On the plant-remains from the Downtonian of England and Wales", Philosophical Transactions of the Royal Society B, 227 (544): 245–291, Bibcode:1937RSPTB.227..245L, doi:10.1098/rstb.1937.0004
- Herron, Scott Freeman, Jon C. (2004). Evolutionary analysis (3rd ed.). Upper Saddle River, NJ: Pearson Education. p. 816. ISBN 978-0-13-101859-4.
- Edwards, D.; Davies, K.L. & Axe, L. (1992), "A vascular conducting strand in the early land plant Cooksonia", Nature, 357 (6380): 683–685, Bibcode:1992Natur.357..683E, doi:10.1038/357683a0, S2CID 4264332
- Libertín, Milan; Kvaček, Jiří; Bek, Jiří; Žárský, Viktor & Štorch, Petr (2018), "Sporophytes of polysporangiate land plants from the early Silurian period may have been photosynthetically autonomous", Nature Plants, 4 (5): 269–271, doi:10.1038/s41477-018-0140-y, PMID 29725100, S2CID 19151297
- Gonez, P. & Gerrienne, P. (2010b), "Aberlemnia caledonica gen. et comb. nov., a new name for Cooksonia caledonica Edwards 1970", Review of Palaeobotany and Palynology, 163 (1–2): 64–72, doi:10.1016/j.revpalbo.2010.09.005
- Wellman, C. H.; Edwards, D. & Axe, L. (1998), "Ultrastructure of laevigate hilate spores in sporangia and spore masses from the Upper Silurian and Lower Devonian of the Welsh Borderland" (PDF), Philosophical Transactions of the Royal Society B, 353 (1378): 1983–2004, doi:10.1098/rstb.1998.0349, PMC 1692433
- Kenrick, Paul & Crane, Peter R. (1997a), The Origin and Early Diversification of Land Plants: A Cladistic Study, Washington, D.C.: Smithsonian Institution Press, ISBN 978-1-56098-730-7
- Taylor, Thomas N. (1988), "The origin of land plants: some answers, more questions", Taxon, 37 (4): 805–833, doi:10.2307/1222087, JSTOR 1222087, cited in Boyce (2008)
- Hao, Shougang & Xue, Jinzhuang (2013), The early Devonian Posongchong flora of Yunnan: a contribution to an understanding of the evolution and early diversification of vascular plants, Beijing: Science Press, pp. 45, 47, ISBN 978-7-03-036616-0, retrieved 2019-10-25