Chondroplon bilobatum Temporal range: | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Phylum: | Cnidaria |
Genus: | † Chondroplon Wade, 1971 |
Species: | †C. bilobatum |
Binomial name | |
†Chondroplon bilobatum Wade, 1971 | |
Chondroplon bilobatum is a medusoid Ediacaran fossil. It has sand-filled tubes, although these may not have been sand-filled in life. It has a shield-like shape, with one end different from the other, and bilateral symmetry, and although it has been suggested that it possesses glide reflection symmetry, such suggestions are based upon a taphonomic effect deforming some specimens. Chondroplon was originally described by Mary Wade in 1971 from fossils found in South Australia. It was named after chondrophores — chitinous floats found on some kinds of colonial floating hydroids.
In addition to the Ediacara Hills in South Australia Chondroplon is also found in the White Sea area of Russia. The host rocks in these areas have been dated as 555 million years old.
The original interpretation was that Chondroplon is a chondrophorine cnidarian. [1] [2] It has also been interpreted as a deformed Dickinsonia. [3] The Vendobionta theory has them as "fluid–filled quilts". As with most of the Ediacaran biota, scientists are yet to reach agreement on a firm classification for this enigmatic fossil.
Dickinsonia is a genus of extinct organism, most likely an animal, that lived during the late Ediacaran period in what is now Australia, China, Russia, and Ukraine. It is one of the best known members of the Ediacaran biota. The individual Dickinsonia typically resembles a bilaterally symmetrical ribbed oval. Its affinities are presently unknown; its mode of growth has been considered consistent with a stem-group bilaterian affinity, though various other affinities have been proposed. It lived during the late Ediacaran. The discovery of cholesterol molecules in fossils of Dickinsonia lends support to the idea that Dickinsonia was an animal, though these results have been questioned.
Charnia is an extinct genus of frond-like lifeforms belonging to the Ediacaran biota with segmented, leaf-like ridges branching alternately to the right and left from a zig-zag medial suture. The genus Charnia was named after Charnwood Forest in Leicestershire, England, where the first fossilised specimen was found. Charnia is significant because it was the first Precambrian fossil to be recognized as such.
Kimberella is an extinct genus of bilaterian known only from rocks of the Ediacaran period. The slug-like organism fed by scratching the microbial surface on which it dwelt in a manner similar to the gastropods, although its affinity with this group is contentious.
Tribrachidium heraldicum is a tri-radially symmetric fossil animal that lived in the late Ediacaran (Vendian) seas. In life, it was hemispherical in form. T. heraldicum is the best known member of the extinct group Trilobozoa.
Spriggina is a genus of early animals whose relationship to living animals is unclear. Fossils of Spriggina are known from the late Ediacaran period in what is now South Australia. Spriggina floundersi is the official fossil emblem of South Australia; it has been found nowhere else.
Vendobionts or Vendozoans (Vendobionta) are a proposed very high-level, extinct clade of benthic organisms that made up of the majority of the organisms that were part of the Ediacaran biota. It is a hypothetical group and at the same time, it would be the oldest of the animals that populated the Earth about 580 million years ago, in the Ediacaran period. They became extinct shortly after the so-called Cambrian explosion, with the introduction of fauna forming groups more recognizably related to modern animals. It is very likely that the whole Ediacaran biota is not a monophyletic clade and not every genus placed in its subtaxa is an animal.
Rangea is a frond-like Ediacaran fossil with six-fold radial symmetry. It is the type genus of the rangeomorphs.
Parvancorina is a genus of shield-shaped bilaterally symmetrical fossil animal that lived in the late Ediacaran seafloor. It has some superficial similarities with the Cambrian trilobite-like arthropods.
Trilobozoa is a phylum of extinct, sessile animals that were originally classified into the Cnidaria. The basic body plan of trilobozoans is often a triradial or radial sphere-shaped form with lobes radiating from its centre. Fossils of trilobozoans are restricted to marine strata of the Late Ediacaran period.
The Ediacaranbiota is a taxonomic period classification that consists of all life forms that were present on Earth during the Ediacaran Period. These were enigmatic tubular and frond-shaped, mostly sessile, organisms. Trace fossils of these organisms have been found worldwide, and represent the earliest known complex multicellular organisms. The term "Ediacara biota" has received criticism from some scientists due to its alleged inconsistency, arbitrary exclusion of certain fossils, and inability to be precisely defined.
Proarticulata is a proposed phylum of extinct, near-bilaterally symmetrical animals known from fossils found in the Ediacaran (Vendian) marine deposits, and dates to approximately 567 to 550 million years ago. The name comes from the Greek προ = "before" and Articulata, i.e. prior to animals with true segmentation such as annelids and arthropods. This phylum was established by Mikhail A. Fedonkin in 1985 for such animals as Dickinsonia, Vendia, Cephalonega, Praecambridium and currently many other Proarticulata are described.
Rugoconites is a genus of Ediacaran biota found as fossils in the form of a circular or oval-like impression preserved in high relief, six or more centimeters in diameter. The fossils are surrounded by frills that have been interpreted as sets of tentacles. The bifurcating radial ribs, spreading from a central dome, serve to distinguish this genus from the sponge Palaeophragmodictya, and may represent the channels of the gastrovascular system. Fossils of Rugoconites have been interpreted as early sponges, although this is countered by Sepkoski et al. (2002), who interpreted the organism as a free-swimming jellyfish-like cnidarian; similar to Ovatoscutum. However, the fossil is consistently preserved as a neat circular form and its general morphology does not vary, therefore a benthic and perhaps slow-moving or sessile lifestyle is more likely. Ivantstov & Fedonkin (2002), suggest that Rugoconites may possess tri-radial symmetry and be a member of the Trilobozoa.
Ediacaran type preservation relates to the dominant preservational mode in the Ediacaran period, where Ediacaran organisms were preserved as casts on the surface of microbial mats.
The Erniettomorphs are a form of Ediacaran fossil consisting of rows of airbed-like tubes arranged along a midline with a glide symmetry. Representative genera include Ernietta, Phyllozoon, Pteridinium, Swartpuntia. Undisputed Erniettomorphs were Ediacaran, but the species Erytholus, Rutgersella, and Protonympha, who have by some been included in this group but are by no means clear members, are found through to the Late Devonian. Their affinity is uncertain; they probably form a clade and are most likely a sister group to the rangeomorphs, which bear a similar construction. Placements within the metazoan crown-group have been rebutted, and it is most likely that these peculiar organisms lie in the stem group to the animals. There is no evidence that they possessed a mouth or gut. Because they may have been found in water which was too deep to permit photosynthesis – and in some cases, lived half-buried in sediment, it is speculated that they fed by osmosis from the sea water. Such a lifestyle requires a very high surface area to volume ratio – higher than is observed in fossils. However, this paradox can be resolved if much of the volume of the organisms was not metabolically active. Many Pteridinium fossils are found completely filled with sand; if this sand were present within the organism while it was alive, this would reduce its metabolically active volume enough to make osmotic feeding viable.
Namalia was first described in 1968 by G. J. B. Germs from an outcrop near Helmeringhausen, Namibia and' dates back to the Ediacaran Period. Namalia has a conical structure and it is thought that it lived semi-buried in sediment along the seafloor.
Ventogyrus is an Ediacaran fossil found in the White Sea-Arkhangelsk region of Russia. It was first discovered in the Teska member of the Ust'-Pinega formation, in a thick lens of sandstone, originally sand dumped by storm waves that cut a deep channel through the shallow sea bottom where the organisms lived. Many individuals were preserved on top of each other, often torn or in distorted positions. As a result, it was originally thought to have had a "boat shaped" form and to have lived anchored in the sea floor. However, a nearby site discovered later by Mikhail Fedonkin yielded separate specimens which were beautifully preserved in an upright position and showed the internal anatomy.
The Ediacaran fossil Hallidaya, a close relative of Skinnera lived in Belomorian of the Late Ediacaran period prior to the Cambrian explosion and thrived in the marine strata on the ocean floor of what is now considered Australia. These fossils were disk-shaped organisms that were slightly dome shaped with tri-radial symmetry. These Ediacaran organisms thrived by living in low-energy inner shelf, in the wave- and current-agitated shoreface, and in the high-energy distributary systems.
Armillifera parva is a species of Ediacaran proarticulate first described by Mikhail Fedonkin in 1980. Its fossils were discovered in the White Sea area, Arkhangelsk Region, Russia. These fossils of A. parva were restricted to almost the same stratigraphic range as Kimberella, although fossils of both organisms have been rarely found.
Eoporpita is a disc or ellipse-shaped Ediacaran fossil with unsure taxonomy/classification. It is known from its type species, Eoporpitamedusa, the only species within the genus Eoporpita.
Conomedusites was a creature from the Ediacaran biota. The Ediacaran period ranged from 635 to 539 million years ago. Its fossil was first discovered in 1966 by Martin F. Glaessner and Mary Wade in South Australia. Conomedusites is believed to have been part of the phylum Cnidaria due to its similar structure to jellyfish and other cnidarians, but this is not known for certain. Conomedusites is thought to have been a stationary osmotroph.