Vale Formation | |
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Stratigraphic range: Early Permian, Leonardian (Kungurian?) | |
Type | Formation |
Unit of | Clear Fork Group |
Sub-units | Standpipe Limestone, Brushy Creek Sandstone, Cedar Top Sandstone |
Underlies | Choza Formation |
Overlies | Arroyo Formation |
Thickness | 160 metres (520 ft) |
Lithology | |
Primary | mudstone, claystone, siltstone |
Other | shale, sandstone, conglomerate |
Location | |
Region | Texas |
Country | United States |
Type section | |
Named for | Vale Post Office (Runnels County) |
Named by | Beede & Waite, 1918 |
The Vale Formation is a geological formation in north-central Texas, a component of the Texas red beds preserving sediments and fossils from the Early Permian Leonardian series. It occupies the middle part of the Clear Fork Group, above the Arroyo Formation and below the Choza Formation. [1] Some sources consider the Vale Formation to be merely an informal subunit of the Clear Fork Formation, thus renaming it to the Middle Clear Fork Formation. [2]
The Vale Formation is named after a former post office in the vicinity of Ballinger in Runnels County. [1] At its broadest conception, the Vale Formation is a unit of primarily terrestrial sediments up to 160 metres (520 ft) thick, [2] stretching from the Texas-Oklahoma border at Wilbarger County, as far south as Runnels County. The base of the Vale Formation is marked by either a limestone bed (the Standpipe Limestone, south of Abilene), or in some northern areas, a sharp unconformity. Likewise, its contact with the Choza Formation is marked by the base of the Bullwagon Dolomite, which is most well-exposed south of Haskell, or by evaporite beds in northern exposures such as Knox County. [3] [1]
Limestone is rare in the fully terrestrial northern red beds, complicating the distinction between the three formations of the Clear Fork Group. [3] To resolve this problem, some geologists, like Nelson et al. (2013), consider the northern part of the Clear Fork Group to be a single formation divided into three informal subunits. [2] In the northern area, major sandstone beds are the most useful stratigraphic markers for distinguishing these informal subunits. The Middle Clear Fork Formation extends from the base of the Brushy Creek Sandstone to the base of the Rt. 1919 Sandstone. Another major sandstone bed, the Cedar Top Sandstone, occurs between these two levels. [2]
As with much of the Texas red beds, the dominant sediments (around 80% by volume) are fine-grained red floodplain deposits such as mudstones, clays, shales, siltstones, and paleosols. Localized beds and lenses of sandstone and conglomerate recorded active meandering river channels, abandoned channels (such as oxbow lakes), and crevasse splays. [3] [1] [4] [2] [5] [6] The conglomerates of the Vale Formation occur in two distinct forms, either large light-colored fragments or (particularly in the northern area) dark brown pebbles derived from the surrounding clay. [3] [7] Light even-bedded clay (pond deposits) may occasionally be found. [3] [1] [2] [8]
Though quite fossiliferous, the fossils of the Vale Formation have not been studied as long as older parts of the Texas red beds, some of which have been prospected since the 1870s. Geologists of the University of Texas discovered the first fossils from the Vale Formation in the 1930s, at the Sid McAdams locality in Taylor County. [9] [1] Since 1946, many more finds were recovered from Knox, Baylor, and Foard counties under the direction of University of Chicago paleontologist Everett C. Olson, who described the northern Vale fossil fauna in detail over the course of the 1950s. [10] [3] [1] Other notable sites include the Stamford locality in Haskell County (discovered by Dalquest and Maymay in 1963), [11] [1] the Blackwood locality in Taylor County (discovered by David Berman in 1970), [1] and the Mud Hill locality (described by Bryan Gee et al. in 2018), also in Taylor County. [12] Over 60 small fossil sites are scattered south of the Clear Fork of the Brazos River. [1]
Synapsids of the Vale Formation | |||
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Genus | Species | Notes | Images |
Casea | C. broilii | A medium-sized caseid. [13] Well-preserved fossils of this species are concentrated within the Cacops bonebed in Baylor County, which may belong to either the upper Arroyo or lower Vale formation. [14] [15] [1] | |
"C." nicholsi [14] | A rare medium-sized caseid, similar to C. broilii but with a larger head, torso, and forelimbs. Known from two closely associated partial skeletons from the upper part of the Vale Formation in Knox County. [14] [15] [1] Phylogenetic analyses suggest that this species is not closely related to Casea broilii, but its fossil material is too fragmentary to warrant a new genus. [16] [17] [18] | ||
Dimetrodon | D. giganhomogenes | A large and fairly common sail-backed sphenacodontid known from various isolated remains and a few partial skeletons which are most similar to Dimetrodon giganhomogenes from the Arroyo Formation. One of the more common fossils of the Sid McAdams and Blackwood localities, with at least 22 individuals from the former site. [1] This species is often misspelled as Dimetrodon gigashomogenes. [13] [19] [3] | |
Ophiacodon? | O.? sp. | A very rare possible ophiacodontid, based on a small humerus from the Sid McAdams locality. If legitimate, it may have been the last surviving member of its family. The next youngest ophiacodontid is Varanosaurus , from the Arroyo Formation. [1] | |
Varanops | V. brevirostris | A large varanopid. [13] Most fossils of this species are concentrated within the Cacops bonebed in Baylor County, which may belong to either the upper Arroyo or lower Vale formation. [1] In addition, an articulated partial skeleton is known from the Mud Hill locality. [20] [21] [12] |
The largest true reptile known from the Vale Formation is an indeterminate moradisaurine captorhinid represented by an enormous tooth plate, at least 11.6 centimetres (4.6 in) in length. [22] This tooth plate was so large it was originally considered to be from an unnamed species of edaphosaurid, which would have made it the youngest known member of that family. [23] As a moradisaurine fossil, it corresponds to a skull around 35 centimetres (14 in) long, larger than Labidosaurikos meachami but smaller than Moradisaurus grandis . [22]
Reptiles of the Vale Formation | |||
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Genus | Species | Notes | Images |
Araeoscelis | A. gracilis | A rare araeoscelidian known from only a few postcranial remains from the Sid McAdams locality. [1] | |
Captorhinikos [24] | "C." cf. chozaensis [24] | A moradisaurine-like captorhinid, likely unrelated to Captorhinikos valensis. [25] Only known from rare tooth-bearing fragments from the Mud Hill locality. [12] | |
C. valensis [24] | A fairly common basal moradisaurine which first appears in the middle part of the Vale Formation. [24] [26] [1] [25] | ||
Captorhinoides [27] | C. valensis [27] | A very rare captorhinid based on a single skull from the middle-upper part of the Vale Formation of Knox County. [27] [24] [26] Possibly a junior synonym of Captorhinus or Captorhinikos. [28] | |
Captorhinus | C. aguti | An uncommon but widespread and geologically long-lived captorhinid. [24] [26] [1] | |
Labidosaurikos | L. barkeri [24] | A fairly common advanced moradisaurine. [24] [1] May be considered a junior synonym of Labidosaurikos meachami, the larger type species which is primarily known from the Early Permian of Oklahoma. [26] | |
cf. Rothianiscus | cf. R. sp. | Tooth plate fragments have been reported from the formation. [1] |
An indeterminate hapsidopareiid microsaur is known from the Mud Hill locality. It is potentially one of the youngest known microsaurs, apart from a few rhynchonkids known from Choza-equivalent strata near Norman, Oklahoma. [12]
Amphibians of the Vale Formation | |||
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Genus | Species | Notes | Images |
Cacops | cf. C. aspidephorus | A eucacopine dissorophid. Well-preserved fossils of Cacops aspidephorus are concentrated within the Cacops bonebed in Baylor County, which may belong to either the upper Arroyo or lower Vale formation. [1] One particularly large partial skeleton is known a site in Baylor County which is assigned to the Vale Formation with more certainty. This larger individual was originally named as a new trematopid species, Trematopsis seltini . [29] [30] [31] | |
Diadectes | D. sp. | An uncommon diadectid diadectomorph, with only a few fossils persisting into the lower part of the formation. [23] [1] [12] | |
Diplocaulus | D. magnicornis | A diplocaulid nectridean with robust blunt-tipped horns. Very common in pond sediments in the lower part of the formation, but not present in subsequent layers, which may indicate extinction via climate change or replacement by potential descendants such as D. recurvatus. [32] [1] | |
D. recurvatus [32] | A diplocaulid nectridean with bent horns tapering to a sharp point. One of the most common fossils in stream sediments from the middle-upper part of the formation, [32] [12] with "literally hundreds" [11] [1] known from the Stamford locality, and many from the Blackwood locality as well. [1] | ||
Eryops | E. megacephalus | A large eryopid temnospondyl, [27] locally common at a few sites such as the Blackwood locality. [1] | |
Gerobatrachus? [33] | G. hottoni [33] | A small amphibamiform known from a partial skeleton. One of the Paleozoic amphibians most similar to lissamphibians (modern amphibians such as frogs, salamanders, and caecilians). [33] Its locality in Baylor County is from the lower half of the Clear Fork Group (Arroyo or Vale formation). | |
Lysorophus | L. tricarinatus | A widespread and locally abundant lysorophian, a type of elongated microsaur predominantly found aestivating in lakeside burrows. [34] [1] The validity of this genus and species has been questioned, and it may be regarded as a junior synonym of Brachydectes . [35] [36] [37] | |
Peronedon | P. primus | A small "keraterpetontid" (diplocaulid) nectridean which is only found at a few particular sites. [38] [1] | |
Seymouria | S. baylorensis | A large seymouriamorph, mostly known from vertebrae and hindlimb material found at the Sid McAdams locality. [1] | |
S. grandis [39] | A large seymouriamorph known from skeletal material found at the Blackwood locality. These fossils were previously misattributed to Labidosaurikos meachami. [39] [1] | ||
Tersomius? | T.? sp. | Various tooth-bearing dissorophid skull fragments from the Sid McAdams locality, similar to Tersomius and Broiliellus . [1] | |
Trimerorhachis | T. insignis | An aquatic dvinosaur which is very common at most sites. [40] [41] [1] [42] | |
T. cf. mesops | A dvinosaur skull from the Stamford locality with several traits (longer snout, absence of an intertemporal bone) comparable to Trimerorhachis mesops. [1] [42] | ||
Waggoneria [27] | W. knoxensis [27] | An uncommon and enigmatic tetrapod with thick vertebrae, a broad otic notch, and multiple rows of teeth on the lower jaw. Its original description compared it to Seymouria, Diadectes, Procolophon , and Labidosaurus , tentatively labeling it as a seymouriamorph. [27] |
Fish of the Vale Formation | |||
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Genus | Species | Notes | Images |
Ctenacanthus | Rare. [1] | ||
Gnathorhiza | G. dikeloda [27] | Common lungfish teeth and skull fragments. First appears at the base of the Vale Formation. [27] [1] | |
G. serrata | Fairly common lungfish teeth, though less abundant than G. dikeloda. [27] [1] | ||
Lawnia [9] | L. taylorensis [9] | A palaeoniscoid actinopterygian known from at least 16 partial skeletons from the Sid McAdams locality. [9] [1] | |
Orthacanthus | O. cf. platypternus | Teeth, fin spines, and skull fragments of a common xenacanth shark. [43] Previously referred to Xenacanthus . [23] [1] |
A few invertebrate fossils are known from the Sid McAdams locality. These include freshwater bivalves (? Palaenodonta ) and a single well-preserved pygocephalomorph crustacean, Mamayocaris jespeni , a species which is abundant in Permian sediments of South Dakota. [1]
Plant fossils of the middle Clear Fork are most well-preserved in fine-grained abandoned river channel deposits. [4] Some abandoned channel sites are dominated by walchian conifers, Taeniopteris , and "comioid" peltasperms ( Auritifolia ). [8] Others have a high proportion of woody gigantopterids ( Evolsonia ), Taeniopteris, and marattialean tree ferns. [6] Tree ferns were probably most specialized for swampy areas alongside permanent water, while conifers occupied dry uplands. Peltasperms and gigantopterids were accustomed to intermediate conditions: well-drained soils with a high water table. [8] [6] A diverse array of insect damage is reported from leaf fossils, with particular preference towards Auritifolia and Taniopteris. [44]
Plants of the Vale Formation | |||
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Genus | Species | Notes | Images |
Auritifolia [45] | A. waggoneria [45] | Large "comioid" peltasperm fronds up to 40 centimetres (16 in) in length. [45] [44] [8] | |
Calamites | C. sp. | Sphenophyte (horsetail) fragments. [4] [46] | |
Callipteris | C. sp. | "Callipterid" seed ferns. [46] | |
Cathaysiopteris [47] | C. yochelsonii [47] | Large gigantopterid leaves up to 20 centimetres (7.9 in) in length. [47] [46] | |
Comia | C. craddockii [48] | Large "comioid" peltasperm fronds up to 30 centimetres (12 in) in length. [48] | |
Cordaites | C. sp. | Strap-shaped leaves of a conifer-like gymnosperm. [46] [8] | |
Evolsonia [49] | E. texana [49] | Very large gigantopterid leaves, at least 80 centimetres (31 in) in length. Previously considered specimens of Gigantopteris. [49] [44] [8] [6] | |
Nanshanopteris | N. sp. | "Supaioid" peltasperm foliage, formerly known as Brongniartites. [46] [8] | |
Odontopteris | O. sp. | Medullosalean fronds of the Mixoneura type. [8] | |
Pecopteris | P. sp. | Marattialean fern leaves. [46] | |
Phasmatocycas? | P.? sp. | A fragmentary branch of a cycad-like gymnosperm, bearing seed-like organs. [50] | |
Rhachiphyllum | R. sp. | Peltasperm foliage. [44] [8] | |
Sandrewia [51] | S. texana [51] | Foliage of a plant of uncertain affinities. [51] [46] [44] | |
Sphenophyllum | S. cf. thonii | Fragmentary foliage of a fern-like plant. [46] [44] [8] [6] | |
Supaia | S. sp. | "Supaioid" peltasperm foliage. [46] [44] [8] | |
Taeniopteris | T. sp. | Smooth-sided leaves of cycad-like gymnosperms. [46] [44] [8] [6] | |
Walchia | W. piniformis | Conifer foliage. [44] [8] |
Cacops, is a genus of dissorophid temnospondyls from the Kungurian stage of the early Permian of the United States. Cacops is one of the few olsoniforms whose ontogeny is known. Cacops fossils were almost exclusively known from the Cacops Bone Bed of the Lower Permian Arroyo Formation of Texas for much of the 20th century. New material collected from the Dolese Brothers Quarry, near Richards Spur, Oklahoma in the past few decades has been recovered, painting a clearer picture of what the animal looked and acted like.
Varanops is an extinct genus of Early Permian varanopid known from Texas and Oklahoma of the United States. It was first named by Samuel Wendell Williston in 1911 as a second species of Varanosaurus, Varanosaurus brevirostris. In 1914, Samuel W. Williston reassigned it to its own genus and the type species is Varanops brevirostris.
Casea is a genus of herbivorous caseid synapsids that lived during the late Lower Permian (Kungurian) in what is now Texas, United States. The genus is only represented by its type species, Casea broilii, named by Samuel Wendell Williston in 1910. The species is represented by a skull associated with a skeleton, a second skull, a partial skull with a better preserved dentition than that of the preceding skulls, and several incomplete postcranial skeletons. Three other Casea species were later erected, but these are considered today to be invalid or belonging to different genera. Casea was a small animal with a length of about 1.20 m and a weight of around 20 kg.
Araeoscelidia or Araeoscelida is a clade of extinct amniotes superficially resembling lizards, extending from the Late Carboniferous to the Early Permian. The group contains the genera Araeoscelis, Petrolacosaurus, the possibly aquatic Spinoaequalis, and less well-known genera such as Kadaliosaurus and Zarcasaurus. This clade is usually considered to be the sister group to all later diapsids.
Cotylorhynchus is an extinct genus of herbivorous caseid synapsids that lived during the late Lower Permian (Kungurian) and possibly the early Middle Permian (Roadian) in what is now Texas and Oklahoma in the United States. The large number of specimens found make it the best-known caseid. Like all large herbivorous caseids, Cotylorhynchus had a short snout sloping forward and very large external nares. The head was very small compared to the size of the body. The latter was massive, barrel-shaped, and ended with a long tail. The limbs were short and robust. The hands and feet had short, broad fingers with powerful claws. The barrel-shaped body must have housed large intestines, suggesting that the animal had to feed on a large quantity of plants of low nutritional value. Caseids are generally considered to be terrestrial, though a semi-aquatic lifestyle has been proposed by some authors. The genus Cotylorhynchus is represented by three species, the largest of which could reach more than 6 m in length. However, a study published in 2022 suggests that the genus may be paraphyletic, with two of the three species possibly belonging to separate genera.
Captorhinus is an extinct genus of captorhinid reptiles that lived during the Permian period. Its remains are known from North America and possibly South America.
Labidosaurikos is a genus of extinct captorhinid tetrapods that lived around 279 to 272 million years ago during Kungurian age of the lower Permian. The American paleontologist John Willis Stovall first described Labidosaurikos in 1950, naming it "Labidosaurus like" for the striking similarity of the holotype skull of his specimen to the cranial anatomy of another captorhinid Labidosaurus hamatus.
Trematopidae is a family of dissorophoid temnospondyls spanning the late Carboniferous to the early Permian. Together with Dissorophidae, the family forms Olsoniformes, a clade comprising the medium-large terrestrial dissorophoids. Trematopids are known from numerous localities in North America, primarily in New Mexico, Oklahoma, and Texas, and from the Bromacker quarry in Germany.
Euryodus is an extinct genus of microsaur within the family Gymnarthridae. Euryodus is a Lepospondyl from the clade Microsauria that lived during the Lower Permian. The name comes from Greek, meaning ‘broad-tooth’. It has been found in the southern half of North America, from its original discovery in Texas up to Utah.
Phonerpeton is an extinct genus of dissorophoid temnospondyl within the family Trematopidae that is known from the early Permian of Texas.
Eosyodon is a dubious genus of extinct non-mammalian synapsids from the Permian of Texas. Its type and only species is Eosyodon hudsoni. Though it was originally interpreted as an early therapsid, it is probably a member of Sphenacodontidae, the family of synapsids that includes Dimetrodon.
Waggoneria is a genus of seymouriamorph from the Early Permian of Texas. It was named by American paleontologist Everett C. Olson in 1951 on the basis of a holotype fossil that included a weathered skull, lower jaws, vertebrae, and part of the pectoral girdle. The type and only species is W. knoxensis. A new family, Waggoneriidae, was also erected for the specimen.
Everett Claire Olson was an American zoologist, paleontologist, and geologist noted for his seminal research of origin and evolution of vertebrate animals. Through his research studying terrestrial vertebrate fossils he identified intervals of extinction in the Permian and Triassic. He developed the concept of chronofauna, which he defined as "a geographically restricted, natural assemblage of interacting animal populations that has maintained its basic structure over a geologically significant period of time". He also proposed stratigraphic correlations between North American and Russian vertebrate-bearing strata for which additional support was found much later. The drop in terrestrial vertebrate diversity he proposed in at the end of the Kungurian stage of the Permian period that occurred 270 million years ago now carries his name - Olson's Extinction. Alternatively, some scientists think that the change was gradual but that it looks abrupt because of a gap in the fossil record, called "Olson's Gap". Some of his other notable research also included the taxa Slaugenhopia, Trimerorhachis, and Waggoneria.
Paleontology in Oklahoma refers to paleontological research occurring within or conducted by people from the U.S. state of Oklahoma. Oklahoma has a rich fossil record spanning all three eras of the Phanerozoic Eon. Oklahoma is the best source of Pennsylvanian fossils in the United States due to having an exceptionally complete geologic record of the epoch. From the Cambrian to the Devonian, all of Oklahoma was covered by a sea that would come to be home to creatures like brachiopods, bryozoans, graptolites and trilobites. During the Carboniferous, an expanse of coastal deltaic swamps formed in areas of the state where early tetrapods would leave behind footprints that would later fossilize. The sea withdrew altogether during the Permian period. Oklahoma was home a variety of insects as well as early amphibians and reptiles. Oklahoma stayed dry for most of the Mesozoic. During the Late Triassic, carnivorous dinosaurs left behind footprints that would later fossilize. During the Cretaceous, however, the state was mostly covered by the Western Interior Seaway, which was home to huge ammonites and other marine invertebrates. During the Cenozoic, Oklahoma became home to creatures like bison, camels, creodonts, and horses. During the Ice Age, the state was home to mammoths and mastodons. Local Native Americans are known to have used fossils for medicinal purposes. The Jurassic dinosaur Saurophaganax maximus is the Oklahoma state fossil.
The Chickasha Formation is a geologic formation in Oklahoma. It preserves fossils dating back to the Roadian stage of the Middle Permian. These include, among others, the dissorophoid temnospondyl Nooxobeia gracilis, the lepospondyl Diplocaulus parvus, and the captorhinid Rothianiscus robusta, initially called Rothia robusta by Olson.
The Archer City Formation is a geological formation in north-central Texas, preserving fossils from the Asselian and early Sakmarian stages of the Permian period. It is the earliest component of the Texas red beds, introducing an tropical ecosystem which will persist in the area through the rest of the Early Permian. The Archer City Formation is preceded by the cool Carboniferous swamp sediments of the Markley Formation, and succeeded by the equally fossiliferous red beds of the Nocona Formation. The Archer City Formation was not named as a unique geological unit until the late 1980s. Older studies generally labelled its outcrops as the Moran or Putnam formations, which are age-equivalent marine units to the southwest.
The Arroyo Formation, sometimes termed the Lower Clear Fork Formation, is a geologic formation in Texas. It preserves fossils dating back to the Kungurian stage of the Permian period. It is the lower-most portion of the Clear Fork Group, part of a series of fossiliferous Permian strata in the south-central United States known as the red beds.
The San Angelo Formation is a geologic formation in Texas. It preserves fossils dating back to the Permian period. Along with the Chickasha Formation is one of the two geologically youngest formations in North America to preserve fossils of caseids, and it is the youngest one to preserve remains of undoubted sphenacodontids, namely, Dimetrodon angelensis.
Richards Spur is a Permian fossil locality located at the Dolese Brothers Limestone Quarry north of Lawton, Oklahoma. The locality preserves clay and mudstone fissure fills of a karst system eroded out of Ordovician limestone and dolomite, with the infilling dating to the Artinskian stage of the early Permian (Cisuralian), around 289 to 286 million years ago. Fossils of terrestrial animals are abundant and well-preserved, representing one of the most diverse Paleozoic tetrapod communities known. A common historical name for the site is Fort Sill, in reference to the nearby military base. Fossils were first reported at the quarry by workers in 1932, spurring a wave of collecting by local and international geologists. Early taxa of interest included the abundant reptile Captorhinus and microsaurs such as Cardiocephalus and Euryodus. Later notable discoveries include Doleserpeton, the most diverse assortment of parareptiles in the Early Permian, and the rare early diapsid Orovenator.