Belemnitina

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Belemnitina
Temporal range: Early Jurassic to Early Cretaceous
Passaloteuthis paxillosa.JPG
Passaloteuthis paxillosa
Scientific classification Red Pencil Icon.png
Kingdom: Animalia
Phylum: Mollusca
Class: Cephalopoda
Order: Belemnitida
Suborder: Belemnitina
Families

Cylindroteuthidae
Hastitidae
Oxyteuthidae
Passaloteuthidae
Salpingoteuthidae

Contents

Belemnitina is a suborder of belemnites, an extinct group of cephalopods. They have been identified as the oldest of all the belemnites and are likely the stockgroup for them. They were extant from the early Jurassic to the early Cretaceous. Their geographic distribution was mostly limited to Europe, although specimens have been described in Japan suggesting they may have been more widespread than previously thought.

Morphology

They have a broad, rounded pro-ostracum (the section of the guard (the hard internal skeleton commonly fossilised) closest to the head of the living animal). [1] This characteristically lacks longitudinal alveolar canals and the associated splitting surfaces or open fissures. Commonly there are one or more longitudinal furrows in the apical region of the guard, similar furrows may be found in the alveolar region, these would not be accompanied by splitting surfaces or open fissures.

Distribution

Based on current evidence it appears that the Belemnitina were mostly restricted to Europe prior to the Toarcian (late-early Jurassic), probably in small shelf seas until the Pliensbachian (middle-early Jurassic). [2] After the middle Jurassic they appear to have spread but still remained primarily in Europe. They gradually retreated during the Jurassic, becoming extinct in the Mediterranean area in the Oxfordian (late Jurassic) times. [3] The last remaining members of the Belemnitina disappear from North-western Europe at the Berremian-Aptian boundary (early Cretaceous).

Stratigraphic range

Belemnitina first appear in the fossil record in the Hettangian (early Jurassic). Two genera, Schwegleria and aff. Subhastites are found in Hettangian sediments from Belgium, southwest Germany and northern Ireland. [4] They are the oldest belemnites thus far found and have been suggested as a stockgroup for all belemnites. Belemnitina have also been found in Hettangian deposits in Japan, which implies an origin for this sub-group before the Jurassic. [4] This fits with the evidence from other groups such as the Belemnitida which have been recorded approximately 33 million years before the Triassic-Jurassic boundary.

There appears to have been a replacement of Belemnitina with the sub-order Belemnopseina in North-western Europe before the Berremian-Aptian boundary. [3] The long interval (47 million years) between the extinction in the Mediterranean region (Oxfordian) and that in North-western Europe (Aptian) implies that the Belemnitina survived in geographically isolated regions. [3]

Related Research Articles

The Cretaceous is a geological period that lasted from about 145 to 66 million years ago (Mya). It is the third and final period of the Mesozoic Era, as well as the longest. At around 79 million years, it is the longest geological period of the entire Phanerozoic. The name is derived from the Latin creta, "chalk", which is abundant in the latter half of the period. It is usually abbreviated K, for its German translation Kreide.

The Jurassic is a geologic period and stratigraphic system that spanned from the end of the Triassic Period 201.3 million years ago (Mya) to the beginning of the Cretaceous Period, approximately 145 Mya. The Jurassic constitutes the middle period of the Mesozoic Era and is named after the Jura Mountains, where limestone strata from the period were first identified.

The Mesozoic Era, also called the Age of Reptiles and the Age of Conifers, is the second-to-last era of Earth's geological history, lasting from about 252 to 66 million years ago and comprising the Triassic, Jurassic and Cretaceous Periods. It is characterized by the dominance of archosaurian reptiles, like the dinosaurs; an abundance of conifers and ferns; a hot greenhouse climate; and the tectonic break-up of Pangaea. The Mesozoic is the middle of three eras since complex life evolved: the Paleozoic, the Mesozoic, and the Cenozoic.

Triassic–Jurassic extinction event Mass extinction ending the Triassic period

The Triassic–Jurassic (Tr-J) extinction event, sometimes called the end-Triassic extinction, marks the boundary between the Triassic and Jurassic periods, 201.3 million years ago, and is one of the major extinction events of the Phanerozoic eon, profoundly affecting life on land and in the oceans. In the seas, the entire class of conodonts and 23–34% of marine genera disappeared. On land, all archosauromorphs other than crocodylomorphs, pterosaurs, and dinosaurs went extinct; some of the groups which died out were previously abundant, such as aetosaurs, phytosaurs, and rauisuchids. Some remaining non-mammalian therapsids and many of the large temnospondyl amphibians had gone extinct prior to the Jurassic as well. However, there is still much uncertainty regarding a connection between the Tr-J boundary and terrestrial vertebrates, due to a paucity of terrestrial fossils from the Rhaetian (latest) stage of the Triassic. What was left fairly untouched were plants, dinosaurs, pterosaurs and mammals; this allowed the dinosaurs and pterosaurs to become the dominant land animals for the next 135 million years.

Brachiosauridae Extinct family of dinosaurs

The Brachiosauridae are a family or clade of herbivorous, quadrupedal sauropod dinosaurs. Brachiosaurids had long necks that enabled them to access the leaves of tall trees that other sauropods would have been unable to reach. In addition, they possessed thick spoon-shaped teeth which helped them to consume tough plants more efficiently than other sauropods. They have also been characterized by a few unique traits or synapomorphies; dorsal vertebrae with 'rod-like' transverse processes and an ischium with an abbreviated pubic peduncle.

Anaxyelidae Family of sawflies

Anaxyelidae is a family of incense cedar wood wasps in the order Hymenoptera. It contains only one living genus, Syntexis, which has only a single species, native to Western North America. Fossils of the family extend back to the Middle Jurassic, belonging to over a dozen extinct genera, with a particularly high diversity during the Early Cretaceous. Syntexis lay eggs in the sapwood of conifers, preferring recently burnt wood.

Cryptobranchoidea Suborder of salamanders

The Cryptobranchoidea are a suborder of salamanders found in Asia, European Russia, and the United States. They are known as primitive salamanders, in contrast to Salamandroidea, the advanced salamanders. It has two living subdivisions, Cryptobranchidae, which includes Asian giant salamanders and hellbenders, and Hynobiidae, commonly known as Asian salamanders.

Cylindroteuthis is a genus of belemnite that lived from the Early Jurassic to the Early Cretaceous. Its fossils have been found in Asia, Europe, North America, and New Zealand.

<i>Clevosaurus</i> Extinct genus of reptiles

Clevosaurus is an extinct genus of rhynchocephalian reptile from the Late Triassic and the Early Jurassic periods. Species of Clevosaurus were widespread across Pangaea, and have been found on all continents except Australia and Antarctica. Five species of Clevosaurus have been found in ancient fissure fill deposits in south-west England and Wales, alongside other sphenodontians, early mammals and dinosaurs. In regards to its Pangaean distribution, C. hadroprodon is the oldest record of a sphenodontian from Gondwana.

Coptoclavidae Extinct family of beetles

Coptoclavidae is an extinct family of aquatic beetles in the suborder Adephaga. The Coptoclavidae lived from the Triassic to the Early Cretaceous. Coptoclavidae is a clade of Dytiscoidea. The increase in the teleost fish population and the competition of Gyrinidae and Dytiscidae is believed to have caused their extinction.

Neuquén Basin

Neuquén Basin is a sedimentary basin covering most of Neuquén Province in Argentina. The basin originated in the Jurassic and developed through alternating continental and marine conditions well into the Tertiary. The basin bounds to the west with the Andean Volcanic Belt, to the southeast with the North Patagonian Massif and to the northeast with the San Rafael Block and to the east with the Sierra Pintada System. The basin covers an area of approximately 120,000 square kilometres (46,000 sq mi). One age of the SALMA classification, the Colloncuran, is defined in the basin, based on the Collón Curá Formation, named after the Collón Curá River, a tributary of the Limay River.

Belemnitida Extinct, squid-like, Mesozoic cephalopods

Belemnitida is an extinct order of squid-like cephalopods that existed from the Late Triassic to Late Cretaceous. Unlike squid, belemnites had an internal skeleton that made up the cone. The parts are, from the arms-most to the tip: the tongue-shaped pro-ostracum, the conical phragmocone, and the pointy guard. The calcitic guard is the most common belemnite remain. Belemnites, in life, are thought to have had 10 hooked arms and a pair of fins on the guard. The chitinous hooks were usually no bigger than 5 mm (0.20 in), though a belemnite could have had between 100 and 800 hooks in total, using them to stab and hold onto prey.

<i>Omma</i> Genus of beetles

Omma is a genus of beetles in the family Ommatidae. Omma is an example of a living fossil. The oldest species known, O. liassicum, lived during the final stage of the Triassic (Rhaetian), over 200 million years ago, though the placement of this species in Omma has been questioned. Numerous other fossil species are known from the Jurassic and Cretaceous of Europe and Asia. The only living species is Omma stanleyi, which is endemic to Australia. Three other extant species endemic to Australia that were formerly part of this genus were moved to the separate genus Beutelius in 2020.Omma stanleyi is strongly associated with wood, being found under Eucalyptus bark and exhibiting thanatosis when disturbed. Its larval stage and many other life details are unknown due to its rarity. Males are typically 14-20 mm in length, while females are 14.4-27.5 mm. Omma stanleyi occurs throughout eastern Australia from Victoria to Central Queensland.

Xinjiangchelyidae Extinct family of turtles

Xinjiangchelyidae is an extinct family of turtles known from the Lower Jurassic to the Middle Cretaceous of Asia and western Europe. They have generally been interpreted as either being basal cryptodires or placed outside of crown Testudines.

The Progonocimicidae are an extinct family of true bugs in the suborder Coleorrhyncha. Progonocimicidae fossils have been found in Europe, Asia, Australia, and South America.

Mesoblattinidae is an extinct family of cockroaches known from the Mesozoic. It was formerly considered a wastebasket taxon for Mesozoic cockroaches, but the family has subsequently been better defined, with many taxa transferred to Caloblattinidae. It is considered to have close affinities with Blattidae and Ectobiidae, as well as possibly Blaberidae.

Lophioneurida is an extinct order of Thysanoptera, dating from the Carboniferous to the Cretaceous. It is likely paraphyletic, with modern thrips having evolved from members of the group.

Orthophlebiidae

Orthophlebiidae is an extinct family of scorpionflies known from the Triassic to Cretaceous, belonging to the superfamily Panorpoidea. The family is poorly defined and is probably paraphyletic, representing many primitive members of Panorpoidea with most species only known from isolated wings, and has such been considered a wastebasket taxon.

Coccolepididae Extinct family of fish

Coccolepididae is an extinct family of ray-finned fish, known from the Early Jurassic to Early Cretaceous, most of which were originally referred to the type genus Coccolepis. They had a widespread distribution, being found in North and South America, Australia, Asia and Europe. They are mostly known from freshwater environments, though several were marine. They are morphologically conservative, and have poorly ossified endo and exoskeletons, which usually results in poor preservation. This makes it difficult to distinguish species. They are generally small fish, with the largest known specimens reaching a length of 210 mm. Historically, they have been classified as members of “Palaeonisciformes”, a paraphyletic grouping of all non-neopterygian fish, due to their plesiomorphic conservative morphology closely resembling those of many other groups of primitive fish. They have been suggested to be relatives of the Acipenseriformes within the Chondrostei.

Peipiaosteidae

Peipiaosteidae is an extinct family of fish, known from the Late Jurassic and Early Cretaceous of Asia. It is considered to be a member of Acipenseriformes, related to sturgeons (Acipenseridae) and paddlefish (Polyodontidae). Fossils have been found in freshwater deposits in China, Russia, Kazakhstan, and Mongolia. They are generally considered either the earliest diverging group of Acipenseriformes, or the sister group to the clade containing Acipenseridae and Polyodontidae.

References

  1. Jeletzky, J. A. (1996). "Comparative morphology, phylogeny, and classification of fossil Coleoidea". The University of Kansas Paleontological Contributions: Article 42 Mollusca 7.
  2. Peter Doyle; Simon R.A. Kelly; Duncan Pirrie; Alberto C. Riccardi (1997). "Jurassic belemnite distribution patterns: implications of new data from Antarctica and Argentina". Alcheringa: An Australasian Journal of Palaeontology. 21 (3): 219–228. doi:10.1080/03115519708619175.
  3. 1 2 3 Jörg Mutterlose (1998). "The Barremian–Aptian turnover of biota in northwestern Europe: evidence from belemnites". Palaeogeography, Palaeoclimatology, Palaeoecology. 144: 161–173. doi:10.1016/s0031-0182(98)00081-9.
  4. 1 2 Yasuhiro Iba; Shin-ichi Sano; Jörg Mutterlose; Yasuo Kondo (2012). "Belemnites originated in the Triassic—A new look at an old group". Geology. 40: 911–914. doi:10.1130/g33402.1.