Siphonotretida

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Siphonotretida
Temporal range: Cambrian Stage 4–Ludlow
Schizambon perspinosum.jpg
"Schizambon" [sic] perspinosum , a siphonotretid from the Upper Ordovician of Oklahoma
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Brachiopoda
Class: Lingulata
Order: Siphonotretida
Kuhn, 1949
Superfamily: Siphonotretoidea
Kutorga, 1848
Family: Siphonotretidae
Kutorga, 1848

Siphonotretida is an extinct order of linguliform brachiopods in the class Lingulata. The order is equivalent to the sole superfamily Siphonotretoidea, itself containing the sole family Siphonotretidae. Siphonotretoids were originally named as a superfamily of Acrotretida, before being raised to their own order. [1]

Contents

Evolution

Spihonotretids were most abundant in the late Cambrian and Early Ordovician (Furongian to Floian), and were traditionally considered to have gone extinct in the Upper Ordovician ("Ashgill"). [1] More recently, new siphonotretids have been described as early as Cambrian Stage 4 ( Schizambon ) [2] [3] and as late as the Ludlow Epoch of the Silurian ( Orbaspina ). [4] [5] Isolated fragments are even known from the Emsian stage of the Lower Devonian. [3] Archaic Cambrian-style siphonotretids such as Schizambon and Helmersenia , with basic forms of ornamentation, populated the shores of Baltica, Laurentia, and Gondwana by the start of the Ordovician. In the late Tremadocian, advanced Ordovician-style spiny siphonotretids spread out from temperate waters around Gondwana and mostly replaced their older relatives. [6] [7]

Anatomy

Siphonotretids had simple, rounded shells, with an ornamentation of hollow spines [1] or rarely pointed tubercles. [3] The shell is usually ventribiconvex (both valves convex, the ventral valve moreso) and composed of microscopic granules of apatite. The inner surface of the shell tends to be weakly mineralized, so many aspects of the musculature and other soft anatomy are difficult to estimate in most species. Available data supports comparison to the internal structures of lingulids. [1] Siphonotretids may be related to the linguloid families Lingulellotretidae or Dysoristidae. [8]

Similar to acrotretides, the pedicle foramen was set at the apex of the ventral valve, though it is often elongated into a tubular groove opening forwards. This groove lies on a triangular extension of the ventral valve, known as a pseudointerarea, which overhangs the dorsal valve. Unlike acrotretides, the adult shell is spinose while the larval shell lacks a pitted texture. [1]

The possible siphonotretid Acanthotretella is known from several exceptionally-preserved specimens which reveal lingulid-like traits such as setae, a spirolophous lophophore and U-shaped gut. However, the shell was poorly mineralized and sends out a very long, stalk-like pedicle, which in one specimen was attached to a fragment of algae. Combined with a lightweight shell, the pedicle likely helped to suspend the body above the seabed, an epibenthic lifestyle dissimilar to the infaunal (burrowing) lingulids. [9] [2] [10]

List of genera

Related Research Articles

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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 Ma to the start of the Silurian Period 443.8 Ma.

The Obolellata are a class of Rhynchonelliform brachiopods with two orders, Obolellida and Naukatida. They are essentially restricted to the lower-middle Cambrian.

<span class="mw-page-title-main">Craniidae</span> Family of shelled animals

The Craniidae are a family of brachiopods, the only surviving members of the subphylum Craniiformea. They are the only members of the order Craniida, the monotypic suborder Craniidina, and the superfamily Cranioidea; consequently, the latter two taxa are at present redundant and rarely used.There are three living genera within Craniidae: Neoancistrocrania, Novocrania, and Valdiviathyris. As adults, craniids either live freely on the ocean floor or, more commonly, cement themselves onto a hard object with all or part of the ventral valve.

<span class="mw-page-title-main">Brachiopod</span> Phylum of marine animals also known as lamp shells

Brachiopods, phylum Brachiopoda, are a phylum of trochozoan animals that have hard "valves" (shells) on the upper and lower surfaces, unlike the left and right arrangement in bivalve molluscs. Brachiopod valves are hinged at the rear end, while the front can be opened for feeding or closed for protection. Two major categories are traditionally recognized, articulate and inarticulate brachiopods. The word "articulate" is used to describe the tooth-and-groove structures of the valve-hinge which is present in the articulate group, and absent from the inarticulate group. This is the leading diagnostic skeletal feature, by which the two main groups can be readily distinguished as fossils. Articulate brachiopods have toothed hinges and simple, vertically oriented opening and closing muscles. Conversely, inarticulate brachiopods have weak, untoothed hinges and a more complex system of vertical and oblique (diagonal) muscles used to keep the two valves aligned. In many brachiopods, a stalk-like pedicle projects from an opening near the hinge of one of the valves, known as the pedicle or ventral valve. The pedicle, when present, keeps the animal anchored to the seabed but clear of sediment which would obstruct the opening.

<span class="mw-page-title-main">Evolution of brachiopods</span> The origin and diversification of brachiopods through geologic time

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The Kirengellids are a group of problematic Cambrian fossil shells of marine organisms. The shells bear a number of paired muscle scars on the inner surface of the valve.

<span class="mw-page-title-main">Acrotretida</span> Extinct order of brachiopods

Acrotretides (Acrotretida) are an extinct order of linguliform brachiopods in the class Lingulata. Acrotretida contains 8 families within the sole superfamily Acrotretoidea. They lived from the Lower Cambrian to the Middle Devonian, rapidly diversifying during the middle Cambrian. In the upper Cambrian, linguliforms reached the apex of their diversity: acrotretides and their relatives the lingulides together comprised nearly 70% of brachiopod genera at this time. Though acrotretides continued to diversify during the Ordovician, their proportional dominance declined, as rhynchonelliforms took on a larger role in brachiopod faunas.

<i>Lingulella</i> Extinct genus of brachiopods

Lingulella is a genus of phosphatic-shelled brachiopod. It is known from the Middle Cambrian Burgess Shale (Canada) to the Upper Ordovician Bromide Formation in North America. 346 specimens of Lingulella are known from the Greater Phyllopod bed, where they comprise 0.66% of the community.

<span class="mw-page-title-main">Rhynchonelliformea</span> Subphylum of brachiopods

Rhynchonelliformea is a major subphylum and clade of brachiopods. It is roughly equivalent to the former class Articulata, which was used previously in brachiopod taxonomy up until the 1990s. These so-called articulated brachiopods have many anatomical differences relative to "inarticulate" brachiopods of the subphyla Linguliformea and Craniformea. Articulates have hard calcium carbonate shells with tongue-and-groove hinge articulations and separate sets of simple opening and closing muscles.

Mickwitziids are a Cambrian group of shelly fossils with originally phosphatic valves, belonging to the Brachiopod stem group, and exemplified by the genus Mickwitzia – the other genera are Heliomedusa and Setatella. The family Mickwitziidae is conceivably paraphyletic with respect to certain crown-group brachiopods.

Stage 10 of the Cambrian is the still unnamed third and final stage of the Furongian series. It follows the Jiangshanian and precedes the Ordovician Tremadocian Stage. The proposed lower boundary is the first appearance of the trilobite Lotagnostus americanus around 489.5 million years ago, but other fossils are also being discussed. The upper boundary is defined as the appearance of the conodont Iapetognathus fluctivagus which marks the beginning of the Tremadocian and is radiometrically dated as 485.4 million years ago.

<span class="mw-page-title-main">Paterinata</span> Extinct class of marine lamp shells

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<span class="mw-page-title-main">Trimerellida</span> Extinct order of brachiopods

Trimerellida is an extinct order of craniate brachiopods, containing the sole superfamily Trimerelloidea and the families Adensuidae, Trimerellidae, and Ussuniidae. Trimerellidae was a widespread family of warm-water brachiopods ranging from the Middle Ordovician to the late Silurian (Ludlow). Adensuidae and Ussuniidae are monogeneric families restricted to the Ordovician of Kazakhstan. Most individuals were free-living, though some clustered into large congregations similar to modern oyster reefs.

Valdiviathyris is a genus of craniate brachiopods that has changed little since the Silurian, from when fossils are known. The extant species V. quenstedti is known from the late Eocene.

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Craniopsidae is an extinct family of craniiform brachiopods which lived from the mid-Cambrian to the Lower Carboniferous (Tournaisian). It is the only family in the monotypic superfamily Craniopsoidea and the monotypic order Craniopsida. If one includes the ambiguous Cambrian genus Discinopsis, craniopsids were the first craniiforms to appear, and may be ancestral to craniids and trimerellides. An even earlier Cambrian genus, Heliomedusa, has sometimes been identified as a craniopsid. More recently, Heliomedusa has been considered a stem-group brachiopod related to Mickwitzia.

<span class="mw-page-title-main">Strophomenata</span> Extinct class of marine lamp shells

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<span class="mw-page-title-main">Kutorginata</span> Extinct genus of shelled animals

Kutorginates (Kutorginata) are an extinct class of early rhynchonelliform ("articulate") brachiopods. The class contains only a single order, Kutorginida (kutorginides). Kutorginides were among the earliest rhynchonelliforms, restricted to the lower-middle part of the Cambrian Period.

Dictyonellida Cooper, 1956 is a brachiopod order within the class Chileata, characterised by a perforation in the ventral valve that is extended through resorption and covered by a colleplax. The dictyonellides are known from the Upper Ordovician to the Lower Permian.

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 2019.

References

  1. 1 2 3 4 5 Holmer, Lars E.; Popov, Leonid E. (2000). "Chapter 1 (part): Lingulata". In Kaesler, Roger L. (ed.). Part H, Brachiopoda (Revised). Volumes 2 & 3: Linguliformea, Craniiformea, and Rhynchonelliformea (part). Treatise on Invertebrate Paleontology. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 136–146. ISBN   0-8137-3108-9.
  2. 1 2 3 Hu, S.; Zhang, Z.; Holmer, L.E.; Skovsted, C.B. (2010). "Soft−part preservation in a linguliform brachiopod from the lower Cambrian Wulongqing Formation (Guanshan Fauna) of Yunnan, South China". Acta Palaeontologica Polonica . 55 (3): 495–505. CiteSeerX   10.1.1.729.8220 . doi:10.4202/app.2009.1106. S2CID   59439966.
  3. 1 2 3 4 5 Holmer, Lars E.; Popov, Leonid E.; Bassett, Michael G. (2007). "Chapter 3 (part): Siphonotretida". In Selden, Paul A. (ed.). Part H, Brachiopoda (Revised). Volume 6: Supplement. Treatise on Invertebrate Paleontology. Boulder, Colorado; Lawrence, Kansas: Geological Society of America; University of Kansas. pp. 2575–2577. ISBN   978-0-8137-3136-0.
  4. 1 2 Mergl, M. (2003). "Orbaspina chlupaci sp. nov., a new siphonotretid brachiopod from the Silurian of the Barrandian area, Bohemia" (PDF). Bulletin of Geosciences. 78 (4): 419–421.
  5. Mergl, M.; Fryda, J.; Kubajko, M. (2018). "Response of organophosphatic brachiopods to the mid-Ludfordian (late Silurian) carbon isotope excursion and associated extinction events in the Prague Basin (Czech Republic)" (PDF). Bulletin of Geosciences. 93 (3): 369–400.
  6. Popov, Leonid E.; Bassett, Michael G.; Holmer, Lars E.; Ghobadi Pour, Mansoureh (2009-08-01). "Early ontogeny and soft tissue preservation in siphonotretide brachiopods: New data from the Cambrian–Ordovician of Iran". Gondwana Research. 16 (1): 151–161. doi:10.1016/j.gr.2009.01.009. ISSN   1342-937X.
  7. Popov, Leonid E.; Holmer, Lars E.; Bassett, Michael G.; Pour, Mansoureh Ghobadi; Percival, Ian G. (2013). Harper, D.A.T.; Servais, T. (eds.). "Chapter 10: Biogeography of Ordovician linguliform and craniiform brachiopods". Geological Society, London, Memoirs. Early Palaeozoic Biogeography and Palaeogeography. 38 (1): 117–126. doi: 10.1144/M38.10 . ISSN   0435-4052.
  8. 1 2 Valentine, James L.; Brock, Glenn (2003). "A new siphonotretid brachiopod from the Silurian of central-western New South Wales, Australia" (PDF). Records of the Australian Museum. 55 (2): 231–244. doi:10.3853/j.0067-1975.55.2003.1378.
  9. 1 2 Holmer, L. E.; Caron, J. B. (2006). "A spinose stem group brachiopod with pedicle from the Middle Cambrian Burgess Shale". Acta Zoologica . 87 (4): 273. doi:10.1111/j.1463-6395.2006.00241.x.
  10. "Acanthotretella spinosa". Burgess Shale Fossil Gallery. Virtual Museum of Canada. 2011. Archived from the original on 2020-11-12.
  11. Streng, Michael; Mellbin, Barbro B.; Landing, Ed; Keppie, J. Duncan (2011). "Linguliform brachiopods from the terminal Cambrian and lowest Ordovician of the Oaxaquia microcontinent (Southern Mexico)". Journal of Paleontology . 85 (1): 122–155. doi:10.1666/10-074.1.