Namacalathus Temporal range: | |
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Scientific classification | |
Domain: | Eukaryota |
Kingdom: | Animalia |
Genus: | † Namacalathus Grotzinger et al., 2000 |
Species: | †N. hermanastes |
Binomial name | |
†Namacalathus hermanastes Grotzinger et al., 2000 | |
Namacalathus [lower-alpha 1] is a problematic metazoan fossil occurring in the latest Ediacaran. The first, and only described species, N. hermanastes, [lower-alpha 2] was first described in 2000 from the Nama Group of central and southern Namibia. [1]
A U–Pb zircon age from the fossiliferous rock in Namibia and Oman provides an age for the Namacalathus zone in the range from 549 to 542 Ma, which corresponds to the Late Ediacaran. Alongside Namapoikia and Cloudina , these organisms are the oldest known evidence in the fossil record of the emergence of calcified skeletal formation in metazoans, a prominent feature in animals appearing later in the Early Cambrian. Shore et al. (2021) reported the first three-dimensional, pyritized preservation of soft tissue in Namacalathus hermanastes from the Nama Group (Namibia), and evaluate the implications of this finding for the knowledge of the phylogenetic relationships of this animal; they suggest it is an ancestor of Lophotrochozoan animals such as brachiopods and worms. [2]
There are only five occurrences of Namacalathus (Namibia, Canada, Oman, Siberia, Paraguay) known to date, all of which are found in association with Cloudina fossils. [1] [3] [4] [5] [6] [7]
Among the late Precambrian fossil assemblage in the Nama group, Namibia, Namacalathus far outnumber Cloudina and other poorly preserved taxa and ichnofossils found in the formation. The Nama Group fossils occur within thrombolitic facies of immense Proterozoic stromatolitic reefs. Namacalathus lived a benthic existence with its stalk attached to the sea floor by means of a holdfast, or possibly to algal mats growing on the reef surface.
The skeleton is believed to have consisted of high-magnesium calcite. [8]
It has a unique shape with a cup on a stalk. The stalk is hollow all the way through and tapered from the bottom, ranging from 1 to 2 mm in diameter, and reaching 30 mm in length. The narrower top of the stalk connects to the cup. The cup is hollow and has a large hole in the top with the shell curving over forming a cup lip. Around the side of the globe are six or seven symmetrically arranged holes, called "windows". The wall curves inwards around each window in a formation called window lips. Each hole is slightly elongated vertically and expanded on the higher side. The size of the cup varies from two to about 25 mm, but averages 6.1 mm. The ratio of the height of the cup to the diameter is from 0.7 to 1.3. The fossil is lightly calcified, preserved as calcite crystals; its original morphology is unknown. [9] The walls in Namacalathus are only 0.1 mm thick, and often deformed by the weight of the sediment. The windows were probably originally filled with organic matter during life, but the cup was likely to be open.
Siberian specimens from the borehole Vostok 3 were designated as new species, because they have, unlike the type species N. hermanastes, a significantly smaller size. Most specimens show sections of the perforated cup, ranging from 110 to 230 μm in diameter; one specimen (with a cup 120 μm across) has a stalk (30 μm in diameter). The walls of the cup are 10 μm thick. [5]
Because the three-dimensional shape of Namacalathus is complex, and the wall is so thin, the fossils appear as a two-dimensional sections in a wide variety of shapes, including closed and open circles, irregular hexagons or heptagons, as well as heart and moon shapes. [10]
Namacalathus was an ecological generalist, able to colonise a variety of settings in the mid- to off-ramp environs, adapting its size to suit the local conditions. [11]
Namacalathus has typically been considered to represent a cnidarian-grade organism, due in part to its propensity for asexual reproduction by budding. Most recently, however (2015), it been interpreted as a lophophorate based on detailed observations of its skeletal construction, which point to accretionary growth in the manner of brachiopods and bryozoans. [8]
The Ediacaran is a geological period of the Neoproterozoic Era that spans 96 million years from the end of the Cryogenian Period at 635 Mya to the beginning of the Cambrian Period at 538.8 Mya. It is the last period of the Proterozoic Eon as well as the last of the so-called "Precambrian supereon", before the beginning of the subsequent Cambrian Period marks the start of the Phanerozoic Eon, where recognizable fossil evidence of life becomes common.
The Neoproterozoic Era is the last of the three geologic eras of the Proterozoic eon, spanning from 1 billion to 538.8 million years ago, and is the last era of the Precambrian "supereon". It is preceded by the Mesoproterozoic era and succeeded by the Paleozoic era of the Phanerozoic eon, and is further subdivided into three periods, the Tonian, Cryogenian and Ediacaran.
The cloudinids, an early metazoan family containing the genera Acuticocloudina, Cloudina and Conotubus, lived in the late Ediacaran period about 550 million years ago. and became extinct at the base of the Cambrian. They formed millimetre-scale conical fossils consisting of calcareous cones nested within one another; the appearance of the organism itself remains unknown. The name Cloudina honors the 20th-century geologist and paleontologist Preston Cloud.
An exoskeleton is a skeleton that is on the exterior of an animal in the form of hardened integument, which both supports the body's shape and protects the internal organs, in contrast to an internal endoskeleton which is enclosed underneath other soft tissues. Some large, hard and non-flexible protective exoskeletons are known as shell or armour.
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.
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.
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.
Namapoikia rietoogensis is among the earliest known animals to produce a calcareous skeleton. Known from the Ediacaran period, before the Cambrian explosion of calcifying animals, the long-lived organism grew up to a metre in diameter and resembles a colonial sponge. It was an encruster, filling vertical fissures in the reefs in which it originally grew.
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.
Ernietta is an extinct genus of Ediacaran organisms with an infaunal lifestyle. Fossil preservations and modeling indicate this organism was sessile and “sack”-shaped. It survived partly buried in substrate, with an upturned bell-shaped frill exposed above the sediment-water interface. Ernietta have been recovered from present-day Namibia, and are a part of the Ediacaran biota, a late Proterozoic radiation of multicellular organisms. They are among the earliest complex multicellular organisms and are known from the late Ediacaran. Ernietta plateauensis remains the sole species of the genus.
The end-Ediacaran extinction is a mass extinction believed to have occurred near the end of the Ediacaran period, the final period of the Proterozoic eon. Evidence suggesting that such a mass extinction occurred includes a massive reduction in diversity of acritarchs, the sudden disappearance of the Ediacara biota and calcifying organisms, and the time gap before Cambrian organisms "replaced" them. Some lines of evidence suggests that there may have been two distinct pulses of the extinction event, one occurring 550 million years ago and the other 539 million years ago.
Palaeopascichnus is an Ediacaran fossil comprising a series of lobes, first originating before the Gaskiers glaciation; it is plausibly a protozoan, but probably unrelated to the classical 'Ediacaran biota'. Once thought to represent a trace fossil, it is now recognized as a body fossil and corresponds to the skeleton of an agglutinating organism.
The small shelly fauna, small shelly fossils (SSF), or early skeletal fossils (ESF) are mineralized fossils, many only a few millimetres long, with a nearly continuous record from the latest stages of the Ediacaran to the end of the Early Cambrian Period. They are very diverse, and there is no formal definition of "small shelly fauna" or "small shelly fossils". Almost all are from earlier rocks than more familiar fossils such as trilobites. Since most SSFs were preserved by being covered quickly with phosphate and this method of preservation is mainly limited to the late Ediacaran and early Cambrian periods, the animals that made them may actually have arisen earlier and persisted after this time span.
The Cambrian explosion is an interval of time approximately 538.8 million years ago in the Cambrian period of the early Paleozoic when a sudden radiation of complex life occurred, and practically all major animal phyla started appearing in the fossil record. It lasted for about 13 to 25 million years and resulted in the divergence of most modern metazoan phyla. The event was accompanied by major diversification in other groups of organisms as well.
Platysolenites is a genus of agglutinated foraminifera known from Ediacaran and lower Cambrian assemblages.
John P. Grotzinger is the Fletcher Jones Professor of Geology at California Institute of Technology and chair of the Division of Geological and Planetary Sciences. His works primarily focus on chemical and physical interactions between life and the environment. In addition to biogeological studies done on Earth, Grotzinger is also active in research into the geology of Mars and has made contributions to NASA's Mars Exploration Program.
The Nama Group is a 125,000 square kilometres (48,000 sq mi) megaregional Vendian to Cambrian group of stratigraphic sequences deposited in the Nama foreland basin in central and southern Namibia. The Nama Basin is a peripheral foreland basin, and the Nama Group was deposited in two early basins, the Zaris and Witputs, to the north, while the South African Vanrhynsdorp Group was deposited in the southern third. The Nama Group is made of fluvial and shallow-water marine sediments, both siliciclastic and carbonate. La Tinta Group in Argentina is considered equivalent to Nama Group.
Nenoxites is an extinct genus of Ediacaran ichnofossils described by Mikhail Fedonkin in 1973. The genus is monotypic; the only species to have been described is Nenoxites curvus.
The Nama assemblage was the last of the Ediacaran biotic assemblages. Following the Avalon and White Sea assemblages, it spanned from c. 550 Ma to c. 539 Ma, coinciding with the Terminal Ediacaran biozone. The assemblage was characterized by a faunal turnover, with the decline of the preexisting White Sea biota. The drop of diversity has been compared to the mass extinctions of the Phanerozoic. A second drop of diversity occurred at the Ediacaran–Cambrian boundary, concluding the Nama assemblages with the end-Ediacaran extinction.