Diploporita

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Diploporita
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Diploporita

Diploporita is an extinct class of blastozoan that ranged from the Ordovician to the Devonian. These echinoderms are identified by a specialized respiratory structure, called diplopores. Diplopores are a double pore system that sit within a depression on a single thecal (body) plate; each plate can contain numerous diplopore pairs. [1]

Contents

The diploporitans likely represent a polyphyletic group. [2] The evidence for this claim lies within the highly morphologically diverse body plans of the diploporitans: there are major differences in the makeup of the attachment structure (e.g., stem or holdfast), in the makeup of the feeding grooves, and even major differences in the construction of the group-defining diplopore respiratory structures. [3] The only phylogenetic analysis of Diploporita to date [4] indicates that Diploporita is not a natural evolutionary group. Rather, Diploporita is an artificial grouping based on the presence of diplopores, that have re-evolved multiple times throughout the echinoderm evolutionary tree.

Evolution

Major Taxonomic Groups

There are three major groups of Diploporita that have been traditionally proposed: the Asteroblastida, Glyptosphaeritida, and the Sphaeronitida. [5] These three groups, which are markedly different from one another, are found in approximately the same age strata in the Early Ordovician of the Prague Basin. Of these proposed groups, only one has been thought to be monophyletic: the Sphaeronitida. This group is characterized by short ambulacral feeding grooves and holdfasts that cement directly to a hard substrate, instead of a stem.

Ancestry

At this time, it is not clear to which group Diploporita is most closely related. It has been suggested that the paraphyletic group Eocrinoidea could have given rise to diploporitans, as well as other groups of blastozoans, but the evidence for this is inconclusive at this time.

Distribution

Information concerning the distribution of diploporitan fossils is constantly changing, as more field sites are found and fossils from these are described. This description of diploporitan fossil occurrences is only meant to be a general introduction and is not an exhaustive list.

Ordovician

Diploporitans in the Ordovician were very diverse, with a high estimate of 176 species. [6] Diploporitans are routinely found preserved from the Ordovician in Gondwana (i.e., southern Europe, northern Africa, the Middle East), Baltica, South China, and European Laurentia (e.g., United Kingdom). Ordovician Occurrences of diploporitans in North American Laurentia are limited to only a very small number of instances. The Late Ordovician Bromide Formation is one of the few, and likely the most well-known, outcrops of diploporitan fossils, Eumorphocystis multiporata [7]

Silurian

The end-Ordovician extinction represented a large-scale extinction for diploporitans. The majority of diploporitan species went extinct during this period and they never returned to their high species numbers after this time. During the Silurian, there was a much larger presence of diploporitans in North American than during the Ordovician. These diploporitans, called the Holocystites Fauna, appeared in North America during the middle of the Silurian. These diploporitans, representing multiple genera, all share the same basic features: reduced food grooves, large plates to support feeding structures that branched off of the surface of the body, and specialized diplopore respiratory structures, called humatipores (diplopores that are connected by multiple canals below the surface of the plate). [8] The Holocystites Fauna is mostly found in the midcontinental United States (e.g., Indiana, Wisconsin, Tennessee) and does not survive past the end of the Silurian.

Paulicystis sparsus, holocystitid diploporitan from middle Silurian rocks of Indiana. Note the humatipore respiratory structures that pierce the plates of the body wall. (University of Iowa Paleontology Repository, SUI 48164) Paulicystissparsus.jpg
Paulicystis sparsus, holocystitid diploporitan from middle Silurian rocks of Indiana. Note the humatipore respiratory structures that pierce the plates of the body wall. (University of Iowa Paleontology Repository, SUI 48164)

Other Silurian occurrences of diploporitans worldwide are rare and limited to only a few species (e.g., Eucystis). These occurrences are largely restricted to southern Europe.

Devonian

Devonian occurrences of diploporitans are also quite rare. Most examples of this are, similar to the Silurian, limited to a few species in southern Europe. It was thought that diploporitans likely went extinct during the Early Devonian. However, a recent discovery found a new genus of diploporitan from the Middle Devonian, 50 million years after the last known diploporitan occurrence, in Kentucky, USA (Laurentia) [9]

Related Research Articles

Ordovician Second period of the Paleozoic Era 485-444 million years ago

The Ordovician is a geologic period and system, the second of six periods of the Paleozoic Era. The Ordovician spans 41.6 million years from the end of the Cambrian Period 485.4 million years ago (Mya) to the start of the Silurian Period 443.8 Mya.

Crinoid Class of echinoderms

Crinoids are marine animals that make up the class Crinoidea, one of the classes of the phylum Echinodermata, which also includes the starfish, brittle stars, sea urchins and sea cucumbers. Those crinoids which, in their adult form, are attached to the sea bottom by a stalk are commonly called sea lilies, while the unstalked forms are called feather stars or comatulids, being members of the largest crinoid order, Comatulida.

Blastoid Extinct class of marine invertebrates

Blastoids are an extinct type of stemmed echinoderm, often referred to as sea buds. They first appear, along with many other echinoderm classes, in the Ordovician period, and reached their greatest diversity in the Mississippian subperiod of the Carboniferous period. However, blastoids may have originated in the Cambrian. Blastoids persisted until their extinction at the end of Permian, about 250 million years ago. Although never as diverse as their contemporary relatives, the crinoids, blastoids are common fossils, especially in many Mississippian-age rocks.

Edrioasteroidea Extinct class of marine invertebrates

Edrioasteroidea is an extinct class of echinoderms. The living animal would have resembled a pentamerously symmetrical disc or cushion. They were obligate encrusters and attached themselves to inorganic or biologic hard substrates.

Stylophora Extinct group of marine invertebrates

The stylophorans are an extinct, possibly polyphyletic group allied to the Paleozoic Era echinoderms, comprising the prehistoric cornutes and mitrates. It is synonymous with the subphylum Calcichordata. Their unusual appearances have led to a variety of very different reconstructions of their anatomy, how they lived, and their relationships to other organisms.

Chasmataspidid

Chasmataspidids, sometime referred to as chasmataspids, are a group of extinct chelicerate arthropods that form the order Chasmataspidida. Chasmataspidids are probably related to horseshoe crabs (Xiphosura) and/or sea scorpions (Eurypterida), with more recent studies suggest that they form a clade (Dekatriata) with Eurypterida and Arachnida. Chasmataspidids are known sporadically in the fossil record through to the mid-Devonian, with possible evidence suggesting that they were also present during the late Cambrian. Chasmataspidids are most easily recognised by having an opisthosoma divided into a wide forepart (preabdomen) and a narrow hindpart (postabdomen) each comprising 4 and 9 segments respectively. There is some debate about whether they form a natural group.

Eocrinoidea Class of echinoderms

The Eocrinoidea are an extinct class of echinoderms that lived between the Early Cambrian and Late Silurian periods. They are the earliest known group of stalked, arm-bearing echinoderms, and were the most common echinoderms during the Cambrian.

Paracrinoidea Extinct class of marine invertebrates

Paracrinoidea is an extinct class of blastozoan echinoderms. They lived in shallow seas during the Early Ordovician through the Early Silurian. While blastozoans are usually characterized by types of respiratory structures present, it is not clear what types of respiratory structures paracrinoids likely had. Despite the taxon's name, the paracrinoids are not closely related to crinoids.

Cystoidea Class of extinct echinoderms

Cystoidea is a class of extinct crinozoan echinoderms, termed cystoids, that lived attached to the sea floor by stalks. They existed during the Paleozoic Era, in the Middle Ordovician and Silurian Periods, until their extinction in the Devonian Period.

Pterygotioidea

Pterygotioidea is a superfamily of eurypterids, an extinct group of aquatic arthropods. Pterygotioids were the most derived members of the infraorder Diploperculata and the sister group of the adelophthalmoid eurypterids. The group includes the basal and small hughmilleriids, the larger and specialized slimonids and the famous pterygotids which were equipped with robust and powerful cheliceral claws.

Rhenopyrgus is an extinct echinoderm in the class Edrioasteroidea, which existed during the Devonian in what is now France and Germany, the Ordovician in Iowa and Illinois, U.S.A.; and the Silurian of Argentina. It was described by Dehm in 1961, and the type species is R. coronaeformis, which was originally described by J. Rievers as a species in the genus Pyrgocystis, in 1961. A new species, R. piojoensis, was described by Colin D. Sumrall, Susana Heredia, Cecilia M. Rodríguez and Ana I. Mestre in 2012, from 116 specimens collected from the Los Espejos Formation in the Loma de Los Piojos locality near San José de Jáchal, Argentina. The species epithet refers to the locality where the specimens were collected from. In 2019 another species, R. viviani, was described by researchers from the Natural History Museum, London, led by Tim Ewin.

<i>Cincinnetina</i> Genus of fossil brachiopods

Cincinnetina is an extinct genus of brachiopods which existed in what is now the United States during the Late Ordovician. It was described by Jisuo Jin in 2012, as a new genus for the Orthis species O. multisecta and O. meeki, each of which have been replaced a number of times under other genera, e.g. Dalmanella, Resserella, and Onniella by other authors. A third species, C. minnesotensis, was described from Minnesota, from which its species epithet was derived.

Paleontology in Wisconsin

Paleontology in Wisconsin refers to paleontological research occurring within or conducted by people from the U.S. state of Wisconsin. The state has fossils from the Precambrian, much of the Paleozoic, and the later part of the Cenozoic. Most of the Paleozoic rocks are marine in origin. Because of the thick blanket of Pleistocene glacial sediment that covers the rock strata in most of the state, Wisconsin’s fossil record is relatively sparse. In spite of this, certain Wisconsin paleontological occurrences provide exceptional insights concerning the history and diversity of life on Earth.

Cincta Extinct class of marine invertebrates

Cincta is an extinct class of echinoderms that lived only in the Middle Cambrian epoch. Homostelea is a junior synonym. The classification of cinctans is controversial, but they are probably part of the echinoderm stem group.

Waeringopteridae

Waeringopteridae is a family of eurypterids, an extinct group of aquatic arthropods. The Waeringopteridae is the only family classified as part of the superfamily Waeringopteroidea, which in turn is classified within the infraorder Diploperculata in the suborder Eurypterina. The earliest known member of the group, Orcanopterus, has been recovered from deposits of Katian age and the latest known surviving member, Grossopterus, has been recovered from deposits of Siegenian age. The name Waeringopteridae is derived from the type genus Waeringopterus, which is named in honor of eurypterid researcher Erik N. Kjellesvig-Waering.

Eurypterina

Eurypterina is one of two suborders of eurypterids, an extinct group of chelicerate arthropods commonly known as "sea scorpions". Members of the suborder are collectively and informally known as "eurypterine eurypterids" or "eurypterines". They are known from fossil deposits worldwide, though primarily in North America and Europe.

Paleontology or palaeontology is the study of prehistoric life forms on Earth through the examination of plant and animal fossils. This includes the study of body fossils, tracks (ichnites), burrows, cast-off parts, fossilised feces (coprolites), palynomorphs and chemical residues. Because humans have encountered fossils for millennia, paleontology has a long history both before and after becoming formalized as a science. This article records significant discoveries and events related to paleontology that occurred or were published in the year 2018.

Soluta (echinoderm) Extinct clade of echinoderms

Soluta is an extinct class of echinoderms that lived from the Middle Cambrian to the Early Devonian. The class is also known by its junior synonym Homoiostelea. Soluta is one of the four "carpoid" classes, alongside Ctenocystoidea, Cincta, and Stylophora, which made up the obsolete subphylum Homalozoa. Solutes were asymmetric animals with a stereom skeleton and two appendages, an arm extending anteriorly and a posterior appendage called a homoiostele.

Ctenocystoidea Extinct clade of marine invertebrates

Ctenocystoidea is an extinct clade of echinoderms, which lived during the Cambrian and Ordovician periods. Unlike other echinoderms, ctenocystoids had bilateral symmetry, or were only very slightly asymmetrical. They are believed to be one of the earliest-diverging branches of echinoderms, with their bilateral symmetry a trait shared with other deuterostomes. Ctenocystoids were once classified in the taxon Homalozoa, also known as Carpoidea, alongside cinctans, solutes, and stylophorans. Homalozoa is now recognized as a polyphyletic group of echinoderms without radial symmetry. Ctenocystoids were geographically widespread during the Middle Cambrian, with one species surviving into the Late Ordovician.

References

  1. Paul, C.R.C. (1972). "Morphology and function of exothecal pore-structures in cystoids". Palaeontology. 15: 1–28.
  2. Paul, C.R.C. (1988). "The phylogeny of the cystoids". Echinoderm Phylogeny and Evolutionary Biology: 199–213.
  3. Sheffield, S.L.; Sumrall, C.D. (2017). "Generic revision of the Holocystitidae of North America (Diploporita, Echinodermata) based on universal elemental homology". Journal of Paleontology: 1–12.
  4. Sheffield, S.L.; Sumrall, C.D. (2019). "The phylogeny of the Diploporita: a polyphyletic assemblage of blastozoan echinoderms". Journal of Paleontology. 93 (4): 740–752. doi:10.1017/jpa.2019.2.
  5. Kesling, R.V. (1967). "Cystoids". The Treatise on Invertebrate Paleontology. Echinodermata S(1): S85–S262.
  6. Lefebvre, B.; et al. (2013). "Palaeobiogeography of Ordovician echinoderms". Geological Society, London, Memoirs. 38: 173–198. doi:10.1144/M38.14. hdl:10261/153355.
  7. Parsley, R. (1982). "Eumorphocystis". Echinoderm Faunas from the Bromide Formation (Middle Ordovician) of Oklahoma: 106–117.
  8. Frest, T.J.; Strimple, H.; Paul, C.R.C. (2011). "The North American Holocystites Fauna (Echinodermata: Blastozoa: Diploporita): Paleobiology and Systematics". Paleontological Research Institution: 151.
  9. Sumrall, C.D.; et al. (2009). "An Enigmatic Blastozoan Echinoderm Fauna from Central Kentucky". Journal of Paleontology. 83 (5): 739–749. doi:10.1666/08-104.1.