Nocona Formation | |
---|---|
Stratigraphic range: Early Permian, Wolfcampian (Sakmarian?–Artinskian?) | |
Type | Formation |
Unit of | Wichita Group |
Underlies | Petrolia Formation |
Overlies | Archer City Formation |
Thickness | 350 ft. |
Lithology | |
Primary | mudstone |
Other | sandstone, siltstone |
Location | |
Region | ![]() |
Country | ![]() |
Type section | |
Named by | Hentz & Brown, 1987 |
The Nocona Formation is a geological formation in Texas, dating back to the Wolfcampian series (Early Permian). As part of the Texas red beds, it is one of several formations renowned for dense bonebeds of terrestrial vertebrate fossils. [1] [2] [3]
The Nocona Formation was named as a distinct geological unit in 1987; its fossil deposits were previously assigned to the Admiral Formation, a time-equivalent marine deposit located further southwest in Texas. The Nocona Formation is considered equivalent to most of the Admiral Formation (apart from the highest few layers), as well as the Coleman Junction Formation. [4] [5] The Nocona Formation overlies the Archer City Formation and underlies the Petrolia Formation. A few sources consider the Nocona Formation to be part of the Archer City Formation, [6] but most regard it as a distinct unit. [7]
Reddish-brown mudstone is the most common rock type in the formation, though grey mudstone and other laminated fine sediments are predominant in bonebeds. 11 distinct layers of dark brown sandstone are thick and extensive enough to be mapped out on a regional scale. The formation is most well-exposed in Archer and Clay counties, extending as far northeast as the Red River which defines the Texas-Oklahoma border. It reaches its thickest extent of around 350 feet in Clay County, where individual sandstone beds can reach a thickness of 40 feet. The most southern extent of the Nocona Formation is the southwestern portion of Archer County. [4] [5] [8]
One particularly notable bonebed is the Geraldine Bonebed in Archer County, discovered by Alfred Sherwood Romer in 1932. [1] Numerous partial and complete skeletons have been recovered from this site, including some of the best fossils of Edaphosaurus boanerges, Archeria crassidisca, Eryops megacephalus , and (to a lesser extent) Dimetrodon natalis . [2] The skeletons are generally preserved in straight, relaxed poses, with the skull aligned towards the east, southwest, or north. Both conditions are similar to modern abrupt mortality events where the animals' corpses end up in permanent bodies of water. Plant debris and charcoal are common in the bonebed as well. It is conceivable that most of the animals killed by a single catastrophe, perhaps a forest fire which polluted the air and water to kill both terrestrial and aquatic animals in the confines of a small lake or pond. [2]
Other productive Nocona Formation bonebeds in Archer County include the Briar Creek Bonebed, [1] Coprolite Bonebed (named for its concentration of shark coprolites), Loftin Bonebed, and Rattlesnake Canyon 2 Bonebed. [3] Their fossil content is more diverse than the Geraldine Bonebed, but also less well-preserved. Unlike the catastrophic scenario implied for Geraldine, these other bonebeds are assumed to be a product of gradual processes of death and decay experienced in calm pond environments. [3]
Color key
| Notes Uncertain or tentative taxa are in small text; |
An egg-like object was discovered by Llewellyn Price in the vicinity of Rattlesnake Canyon, and subsequently described by Romer and Price in 1939. It had a shell-like texture which was not easily comparable to nodules from the Permian of Texas, and the authors considered it to have potentially been laid by a "pelycosaur". If this identification is correct, it is the oldest amniotic egg in the fossil record. [9] [1] Later investigations concluded that a distinct calcareous shell layer was not present, though the high concentration of phosphorus in the object suggests that it may still be an egg, albeit one with a softer outer membrane. [10] [3]
Synapsids of the Nocona Formation | ||||
---|---|---|---|---|
Genus | Species | Localities | Notes | Images |
Ctenorhachis [11] | C. jacksoni [11] | Lake Kickapoo [11] | A large sphenacodontid with a rather low neural spine sail. | ![]() |
Dimetrodon | D. booneorum | Briar Creek [1] [12] | A medium-sized sphenacodontid of uncertain validity. | |
D. limbatus [1] | Briar Creek?, [1] [12] [13] Coprolite, Loftin, Rattlesnake Canyon 2 [3] | A large sphenacodontid with a tall neural spine sail. | ![]() | |
D. natalis | Geraldine, [2] [8] Briar Creek, [1] [12] [13] Rattlesnake Canyon 2 [3] | A small sphenacodontid with a tall neural spine sail. Represented by three partial skeletons. Sometimes regarded as a juvenile of D. limbatus, [2] [3] but confirmed to be a unique species with small adults, according to histological analyses. [12] | ![]() | |
Edaphosaurus | E. boanerges [1] | Geraldine, [1] [2] [14] [8] Briar Creek, [1] [13] Coprolite, Loftin, Rattlesnake Canyon 2? [3] | A medium-sized herbivorous edaphosaurid. [1] [14] One of the most common and characteristic fossils of the Geraldine bonebed, with multiple articulated skeletons displayed in museums around the world. [2] | |
Lupeosaurus | L. kayi | Briar Creek, [1] Coprolite? [3] | A large edaphosaurid known from rare fragments. | ![]() |
Ophiacodon | O. retroversus | Rattlesnake Canyon [1] [15] | An ophiacodontid. | ![]() |
O. uniformis | (vicinity of) Geraldine, [2] [8] Briar Creek [1] [15] | An ophiacodontid. | ![]() | |
Secodontosaurus | S. obtusidens | Briar Creek [1] [12] | A medium-sized sphenacodontid. | ![]() |
Reptiles of the Nocona Formation | ||||
---|---|---|---|---|
Genus | Species | Localities | Notes | Images |
Araeoscelis | A. casei [16] | Godwin Creek [16] | An araeoscelidian initially named as a new genus, Ophiodeirus. [16] | ![]() |
Bolosaurus | B. striatus | Geraldine, [2] [8] Briar Creek, Godwin Creek [17] | A bolosaurid parareptile. | ![]() |
Captorhinidae indet. | Loftin [3] | Rare captorhinid vertebrae. [18] [3] |
Amphibians of the Nocona Formation | ||||
---|---|---|---|---|
Genus | Species | Localities | Notes | Images |
Archeria | A. crassidisca | Geraldine, [19] [2] [14] [8] Briar Creek, [20] Coprolite, Loftin, Rattlesnake Canyon 2 [3] | A large archeriid embolomere. Multiple articulated skeletons have been found in the Geraldine bonebed, representing the most complete and well-described fossils of this species. [19] [2] [14] | ![]() |
Cardiocephalus | C. sp. | Geraldine [8] | Rare microsaur teeth. | |
Diadectes | D. sideropelicus | Geraldine, [2] Briar Creek, [20] Coprolite, Loftin, Rattlesnake Canyon 2 [3] | A large diadectid diadectomorph. | ![]() |
Diplocaulus | D. sp. | Loftin [3] | A diplocaulid nectridean. | |
Eryops | E. megacephalus | Geraldine, [2] [8] Briar Creek, [20] Coprolite, Loftin, Rattlesnake Canyon 2 [3] | An eryopid, a type of large semiaquatic temnospondyl. Articulated skeletons and other remains are common in the Geraldine bonebed. [2] | ![]() |
Rubeostratilia [21] | R. texensis [21] | "east of Henrietta" [21] | An amphibamiform, a type of small terrestrial temnospondyl. | ![]() |
Scapanops [22] | S. neglecta [22] | Halsell Hill [22] | A eucacopine dissorophid, a type of small terrestrial temnospondyl. Previously consider a specimen of Conjunctio . [22] | |
Trimerorhachis | T. insignis | (vicinity of) Geraldine, [2] [8] Godwin Creek, [23] Rattlesnake Canyon, [23] Loftin, Rattlesnake Canyon 2 [3] [23] | A trimerorhachid dvinosaur, a type of small aquatic temnospondyl. | |
Zatrachys | Z. serratus | (vicinity of) Geraldine, [2] Rattlesnake Canyon 2 | A zatracheid temnospondyl, a type of medium-sized terrestrial temnospondyl. | ![]() |
Indeterminate palaeoniscoids are known from the Geraldine, [8] Coprolite, Loftin, and Rattlesnake Canyon 2 bonebeds. [3] Iniopterygian tooth whorls have been reported from the Rattlesnake Canyon area. [8]
Fish of the Nocona Formation | ||||
---|---|---|---|---|
Genus | Species | Localities | Notes | Images |
Acanthodes | A. sp. | Geraldine [8] | Acanthodian fin spines and scales | ![]() |
Barbclabornia | B. luedersensis | Rattlesnake Canyon [24] | Rare xenacanth shark teeth | |
Ectosteorhachis | E. nitidus | Geraldine, [2] Coprolite, Loftin [3] | A megalichthyid tetrapodomorph | |
Helodus | H. sp. | Geraldine [8] | Rare holocephalan teeth | |
Hybodus | H. sp. | Coprolite [3] | A hybodont shark | |
Janassa? | J.? sp. | Geraldine [8] | A single petalodont tooth | |
Orthacanthus | O. platypternus | Geraldine [8] | Xenacanth shark teeth | ![]() |
O. texensis | Geraldine, [2] [8] Briar Creek, [8] Coprolite, [25] Loftin, Rattlesnake Canyon 2 [3] | Very common xenacanth shark teeth and coprolites | ||
Platysomus? | P.? sp. | Geraldine [8] | A single palaeoniscoid tooth | |
Progyrolepis | P. tricessimalaris [26] | Rattlesnake Canyon [26] | A palaeoniscid known from a partial skeleton. | |
Sagenodus | S. periprion | (vicinity of) Geraldine, [2] [8] Coprolite, Rattlesnake Canyon 2 [3] | Lungfish teeth | |
Spermatodus | S. pustulosus | Rattlesnake Canyon 2 [3] | A coelacanth | |
Xenacanthus | X. sp. | Geraldine [8] | Xenacanth shark spine fragments | ![]() |
Plant fossils are known from several bonebeds of the Nocona Formation, though they are subordinate to vertebrate fossils at most sites. [27] [2] Insect damage has been recorded on leaves from the Coprolite Bonebed. It is uncommon (only a third as frequent as in modern plants), even when compared to only slightly younger sites such as the Taint locality in the Waggoner Ranch Formation. Despite the rarity of insect damage, the Coprolite Bonebed shows the oldest occurrence of skeletonization (removal of all but the veins), as well as galls, which are rarely found in Permian plant fossils. [28]
Plants of the Nocona Formation | ||||
---|---|---|---|---|
Genus | Species | Localities | Notes | Images |
Annularia | A. cf. stellata | Geraldine, [2] Coprolite [28] | Foliage of a large calamitacean sphenophyte (horsetail) which formed thickets in shallow water and shorelines. | |
Autunia | A. cf. conferta | Geraldine, [2] Coprolite [28] | Foliage of a peltasperm "seed fern", previously considered a species of Callipteris. [2] Abundant in the Geraldine and Coprolite bonebeds. [2] [28] | |
Calamites | C. undulatus | Geraldine, [2] Coprolite [3] [28] | Common stem impressions of a large calamitacean sphenophyte (horsetail) which formed thickets in shallow water and shorelines. | |
Callipteridium | C. cf. pteridium | Geraldine [2] | Foliage of a medullosalean "seed fern". | |
C. virginianum | Geraldine [2] | Foliage of a medullosalean "seed fern". | ||
Cordaites | C. principalis | Geraldine, [2] Coprolite [28] | Foliage of a cordaitalean gymnosperm, a small tree found in both swamps and uplands. Common in the Geraldine and Coprolite bonebeds. [2] [28] | |
Dadoxylon | D. sp. | Geraldine, [2] Rattlesnake Canyon 2 [3] | Conifer wood and charcoal. | |
Odontopteris | O. genuina | Geraldine [2] | Foliage of a medullosalean "seed fern". | |
O. cf. lingulata | Coprolite [3] | Foliage of a medullosalean "seed fern". | ||
O. cf. osmundaeformis | Geraldine [2] | Foliage of a medullosalean "seed fern". | ||
Pecopteris | P. arborescens | Geraldine [2] | Foliage of a marattialean tree fern, among the most common trees in Permian swamp environments. | |
P. candolleana | Geraldine [2] | |||
P. hemitelioides | Geraldine, [2] Coprolite [3] [28] | |||
P. unita | Geraldine [2] | |||
Psaronius | P. sp. | Geraldine, [2] Loftin [3] | Stems and roots of a marattialean tree fern, likely the same plant which produced Pecopteris leaves. [3] | |
Russellites [29] | R. taeniata | Geraldine, [2] Coprolite [28] | Foliage of a cycadophyte, previously referred to Tingia. Common in the Coprolite Bonebed. [28] | |
Samaropsis | S. spp. | Geraldine [2] | Two species of gymnosperm seeds, possibly from the same plants as Walchia and Cordaites. [2] | |
Sigillaria | S. brardii | Geraldine [2] | Bark and stems of a lycophyte. | |
Sphenophyllum | S. oblongifolium | Geraldine [2] | Foliage of a fern. | |
Sphenopteris | S. cf. macilenta | Geraldine [2] | Foliage of a fern or "seed fern". | |
Walchia | W. piniformis | Geraldine, [2] Coprolite [3] [28] | Foliage of an early conifer, a small tree accustomed to dry uplands. Associated stems and charcoal show similarity to the form genus Schizodendron. [3] Very common in the Geraldine and Coprolite bonebeds. [2] [28] |
Dimetrodon is an extinct genus of non-mammalian synapsid belonging to the family Sphenacodontidae that lived during the Cisuralian age of the Early Permian period, around 295–272 million years ago. With most species measuring 1.7–4.6 m (5.6–15.1 ft) long and weighing 28–250 kg (62–551 lb), the most prominent feature of Dimetrodon is the large neural spine sail on its back formed by elongated spines extending from the vertebrae. It was an obligate quadruped and had a tall, curved skull with large teeth of different sizes set along the jaws. Most fossils have been found in the Southwestern United States, the majority of these coming from a geological deposit called the Red Beds of Texas and Oklahoma. More recently, its fossils have also been found in Germany and over a dozen species have been named since the genus was first erected in 1878.
Edaphosaurus is a genus of extinct edaphosaurid synapsids that lived in what is now North America and Europe around 303.4 to 272.5 million years ago, during the Late Carboniferous to Early Permian. American paleontologist Edward Drinker Cope first described Edaphosaurus in 1882, naming it for the "dental pavement" on both the upper and lower jaws, from the Greek edaphos έδαφος and σαῦρος ("lizard").
Dissorophidae is an extinct family of medium-sized temnospondyls that flourished during the late Carboniferous and early Permian periods. The clade is known almost exclusively from North America.
Sphenacodontidae is an extinct family of sphenacodontoid synapsids. Small to large, advanced, carnivorous, Late Pennsylvanian to middle Permian "pelycosaurs". The most recent one, Dimetrodon angelensis, is from the latest Kungurian or, more likely, early Roadian San Angelo Formation. However, given the notorious incompleteness of the fossil record, a recent study concluded that the Sphenacodontidae may have become extinct as recently as the early Capitanian. Primitive forms were generally small, but during the later part of the early Permian these animals grew progressively larger, to become the top predators of terrestrial environments. Sphenacodontid fossils are so far known only from North America and Europe.
Ophiacodon is an extinct genus of synapsid belonging to the family Ophiacodontidae that lived from the Late Carboniferous to the Early Permian in North America and Europe. The genus was named along with its type species O. mirus by paleontologist Othniel Charles Marsh in 1878 and currently includes five other species. As an ophiacodontid, Ophiacodon is one of the most basal synapsids and is close to the evolutionary line leading to mammals.
Ctenospondylus is an extinct genus of sphenacodontid synapsid
Sphenacodon is an extinct genus of synapsid that lived from about 300 to about 280 million years ago (Ma) during the Late Carboniferous and Early Permian periods. Like the closely related Dimetrodon, Sphenacodon was a carnivorous member of the Eupelycosauria family Sphenacodontidae. However, Sphenacodon had a low crest along its back, formed from blade-like bones on its vertebrae instead of the tall dorsal sail found in Dimetrodon. Fossils of Sphenacodon are known from New Mexico and the Utah–Arizona border region in North America.
Mycterosaurus is an extinct genus of amniotes belonging to the family Varanopidae. It is classified in the varanopid subfamily Mycterosaurinae. Mycterosaurus is the most primitive member of its family, existing from 290.1 to 272.5 MYA, known to Texas and Oklahoma. It lacks some features that its advanced relatives have.
Platyhystrix is an extinct temnospondyl amphibian with a distinctive sail along its back, similar to the unrelated synapsids, Dimetrodon and Edaphosaurus. It lived during the boundary between the latest Carboniferous and earliest Permian periods throughout what is now known as the Four Corners, Texas, and Kansas about 300 million years ago.
The Lystrosaurus Assemblage Zone is a tetrapod assemblage zone or biozone which correlates to the upper Adelaide and lower Tarkastad Subgroups of the Beaufort Group, a fossiliferous and geologically important geological Group of the Karoo Supergroup in South Africa. This biozone has outcrops in the south central Eastern Cape and in the southern and northeastern Free State. The Lystrosaurus Assemblage Zone is one of eight biozones found in the Beaufort Group, and is considered to be Early Triassic in age.
Archeria is a genus of embolomere which lived in the Early Permian of Texas and Oklahoma. It was a medium-sized aquatic predator, with an elongated body and tail. The limbs were proportionally small but well-developed, connected to robust limb girdles. The skull was moderately long and low, up to 30 cm in length. Unlike most embolomeres, Archeria had many small chisel-shaped teeth instead of large fangs.
Wann Langston Jr. was an American paleontologist and professor at the University of Texas at Austin.
Broiliellus is an extinct genus of dissorophoid temnospondyl within the family Dissorophidae. Broiliellus is most closely related to the genus Dissorophus, and both have been placed in the subfamily Dissorophinae. Broiliellus is known from five species from the Early Permian: the type species is Broiliellus texensis, and the other species are Broiliellus brevis,Broiliellus olsoni, Broiliellus arroyoensis, and Broiliellus reiszi. An additional species, Broiliellus novomexicanus, which was originally named Aspidosaurus novomexicanus, is now thought to fall outside the genus as a member of the subfamily Eucacopinae.
Phonerpeton is an extinct genus of dissorophoid temnospondyl within the family Trematopidae that is known from the early Permian of Texas.
Rubeostratilia is an extinct genus of amphibamiform temnospondyl from the early Permian of Texas. It is known from a single skull. This genus was named by Hélène Bourget and Jason S. Anderson in 2011, and the type species is Rubeostratilia texensis. The genus name comes from the Latin translation of 'redbeds' in reference to the Texas redbeds that produced both the holotype and many other early Permian fossils. The specific name is for the state of Texas. The holotype and only known specimen was collected in 1941 from the Nocona Formation exposures in Clay County by a Works Projects Administration project that was transferred to the Field Museum of Natural History through an interinstitutional exchange with the Texas Memorial Museum.
The Red Beds of Texas and Oklahoma are a group of Early Permian-age geologic strata in the southwestern United States cropping out in north-central Texas and south-central Oklahoma. They comprise several stratigraphic groups, including the Clear Fork Group, the Wichita Group, and the Pease River Group. The Red Beds were first explored by American paleontologist Edward Drinker Cope starting in 1877. Fossil remains of many Permian tetrapods have been found in the Red Beds, including those of Dimetrodon, Edaphosaurus, Seymouria, Platyhystrix, and Eryops. A recurring feature in many of these animals is the sail structure on their backs.
The Waggoner Ranch Formation is a geologic formation in northern Texas. It preserves fossils dating back to the Artinskian to Kungurian stages of the Permian period.
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 a 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.