Tortotubus | |
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A leading filament of T. protuberans with primary branches and nascent secondary branches. 250 μm long. | |
T. protuberans from the Silurian of Kerrera, Scotland, with the main filament beginning to be covered by secondary branches and a surrounding envelope. 200 μm long. | |
Scientific classification | |
Kingdom: | |
Subkingdom: | |
Genus: | Tortotubus Johnson, 1985 |
Species | |
T. protuberans |
Tortotubus is an early (Ordovician to Devonian) terrestrial fungus. Its growth trajectory can be ascertained from its fossils, which occur across the globe from the Ordovician to the Devonian. [1] These fossils document foraging activities of slender, cell-wide exploratory hyphae; when these hit a source of food, they produced secondary branches that grew back down the original filament, covered themselves with an envelope, and served as pipes to shuttle nutrients to other parts of the organism. [1] Today, mycelium with this growth pattern is observed in the mushroom-forming fungi. [1]
The form genus Ornatifilum was erected by Burgess and Edwards in 1991 to describe tubular fossils retrieved by acid maceration from the late Silurian. [2] It was originally intended as a form genus, to facilitate stratigraphy and environmental reconstruction; the fossils do not display enough features to classify them confidently, even at a kingdom level. [2]
Fossils first described as Ornatifilum lornensis correspond to the foraging hyphae of Tortotubus. They are tubes of around 10 μm diameter, with an ornamented, granular surface texture. These fossils were compared to late Silurian (Ludlow epoch) fossils retrieved from the Burgsvik beds by Sherwood-Pike and Gray, [3] and the genus was used when similar fossils were recovered from the Scottish island of Kerrera by Charles Wellman ten years later. [4] Similar, unornamented filaments are known from the USA. [5] They have a complex appearance: surface ornament – which covers most of the surface uniformly – takes an array of forms, with "grana, coni, spinae verrucae and occasionally plia" [note 1] present. [4] Further, side-branches and the flask-shaped protuberances occasionally protrude from the tubes, on which the ornament is larger (2.5 μm rather than ~1 μm). [4] Such branching typically occurs in pairs across the main thread. [4]
Fossils originally referred to Tortotubus protuberans represent the mature cords of the fungus, composed of a braid of simple filaments that have merged into one another and formed an outer envelope with a distinctive pustular texture.
A fungal affinity is further established by the presence of punctate spores, which restricts their affinities to the red algae and fungi. The structure of the cell wall is also fungus-like. [1]
Further circumstantial evidence may corroborate a fungal affinity: some fossils have been found in association with fungal spores, [3] and they occur only in settings with a strong terrestrial influence. [1]
In March 2016, scientists from the University of Cambridge found examples of Tortotubus on Gotland, Sweden and Kerrera in the Inner Hebrides, which at 440 million years-old are the oldest examples of a land-dwelling species ever found. [6]
A rich diversity of fungi is known from the lower Devonian Rhynie chert, but the previous record is absent. Since fungi don't biomineralise, they do not readily enter the fossil record; aside from Ornatifilum, there are only two other claims of early fungi. One from the Ordovician [7] has been dismissed on the grounds that it lacks any distinctly fungal features, and is held by many to be contamination; [8] the position of a "probable" Proterozoic fungus is still not established, [8] and it may represent a stem group fungus. If the case for Ornatifilum's fungal affinity were affirmed, that would make it the oldest known fossil fungus – although, since the fungi form a sister group to the animals, the two lineages must have diverged before the first animal lineages, which are known from fossils as early as the Ediacaran. [9]
Lycopodiopsida is a class of herbaceous vascular plants known as lycopods, lycophytes or other terms including the component lyco-. Members of the class are called clubmosses, firmosses 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 formed huge forests that dominated the landscape and contributed to coal deposits.
Acritarchs are organic microfossils, known from approximately 1800 million years ago to the present. Their diversity reflects major ecological events such as the appearance of predation and the Cambrian explosion.
Chitinozoa are a taxon of flask-shaped, organic walled marine microfossils produced by an as yet unknown organism. Common from the Ordovician to Devonian periods, the millimetre-scale organisms are abundant in almost all types of marine sediment across the globe. This wide distribution, and their rapid pace of evolution, makes them valuable biostratigraphic markers.
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.
Prototaxites is a genus of terrestrial fossil fungi dating from the Middle Ordovician until the Late Devonian periods, approximately 470 to 360 million years ago. Prototaxites formed small to large trunk-like structures up to 1 metre (3 ft) wide, reaching 8 metres (26 ft) in height, made up of interwoven tubes around 50 micrometres (0.0020 in) in diameter, making it by far the largest land-dwelling organism of its time.
Tortilicaulis is a moss-like plant known from fossils recovered from southern Britain, spanning the Silurian-Devonian boundary. Originally recovered from the Downtonian of the Welsh borderlands, Tortilicaulis has since been recovered in the famous Ludlow Lane locality.
Nematothallus is a form genus comprising cuticle-like fossils. Some of its constituents likely represent red algae, whereas others resemble lichens.
Ornatifilum is an artificial form genus, which is used to categorise any small, branched filaments with external ornamentation.
Rhynia is a single-species genus of Devonian vascular plants. Rhynia gwynne-vaughanii was the sporophyte generation of a vascular, axial, free-sporing diplohaplontic embryophytic land plant of the Lower Devonian that had anatomical features more advanced than those of the bryophytes. Rhynia gwynne-vaughanii was a member of a sister group to all other eutracheophytes, including modern vascular plants.
The evolution of fungi has been going on since fungi diverged from other life around 1.5 billion years ago, with the glomaleans branching from the "higher fungi" at ~570 million years ago, according to DNA analysis. Fungi probably colonized the land during the Cambrian, over 500 million years ago,, and possibly 635 million years ago during the Ediacaran, but terrestrial fossils only become uncontroversial and common during the Devonian, 400 million years ago.
Salopella is a form genus for small fossil plants of Late Silurian to Early Devonian age. The diagnostic characters are naked axes branching isotomously, terminating in fusiform sporangia. The sporangia are unbranched, but in at least the type species the axes seem to branch just under the sporangia. It differs from the similar form genus Tortilicaulis in that the sporangia do not have spirally arranged cells, and from other similar form genera such as Cooksonia, Uskiella and Tarrantia in the shape of the sporangia.
Adoketophyton is a genus of extinct vascular plants of the Early Devonian. The plant was first described in 1977 based on fossil specimens from the Posongchong Formation, Wenshan district, Yunnan, China. These were originally named Zosterophyllum subverticillatum; later the species was transferred to a new genus as Adoketophyton subverticillatum. One cladistic analysis suggested that it is a lycophyte, related to the zosterophylls. Other researchers regard its placement within the vascular plants as uncertain.
Grisellatheca was a genus of land plant with branching axes. It is known from charcoalified Early Devonian deposits, its type locality being the Brown Clee Hill lagerstatten. Its Terahedraletes spores form permanent tetrads.
Fusitheca was a genus of land plant with branching axes. It is known from charcoalified Early Devonian deposits, its type locality being the Brown Clee Hill lagerstätten. Its spores form smooth-walled, unfused, naked dyads. Its axis comprises length-parallel filaments, and their dichotomies are T-shaped, with the branches bending to continue upwards.
Dutoitia is a genus of Devonian rhyniophyte, named after the renowned South African geologist Alex du Toit. It is one of the earliest plants from Gondwana to colonize land. Its fossils were preserved in fine mudstones of the 400-million-year-old Bokkeveld and Witteberg Groups of South Africa. This erect, gracile plant is less than 10 cm high and very simple in structure. Its diminutive stems, which are devoid of leaflike appendages, branch in two and end in club- or cup-shaped sporangia, occasionally containing its reproductive spores. Stomata are present in the cuticle of their stems for gas exchange, and primitive cells inside the stems transported water from the roots to the aerial parts of the plant. Three species are recognized, D. pulchra Hoeg 1930, D. alfreda Plumstead 1967 and D. maraisia Plumstead 1967.
Odonax was a genus of Early Devonian Zosterophyll with branching axes. It bore kidney-shaped sporangia and spiny branches.
Foozia was a genus of vascular Emsian land plant with a main axis and a number of branches that sub-divide at most once. Some of these bear oval to semicircular sporangia containing Dibolisporites echinaceus, whereas the sterile branches may represent an early foray into leaf-formation. The only known fossils herald from Belgium. It is currently unclassified.
Psilophytites is a form genus of extinct plants; it was created by Høeg for spiny stems (axes) which cannot be assigned to a more precise genus or species, usually because spore-forming organs or sporangia are not present.
Angochitina is an extinct genus of chitinozoans. It was described by Alfred Eisenack in 1931.
The barinophytes are a group of extinct vascular plants (tracheophytes). Their relationship with other vascular plants is unclear. They have been treated as the separate class Barinophytopsida, the order Barinophytales of uncertain class and as a family or clade Barinophytaceae within the zosterophylls. They have also been considered to be possible lycopodiopsids.