Arroyo Formation | |
---|---|
Stratigraphic range: | |
Type | Formation |
Unit of | Clear Fork Group |
Underlies | Vale Formation |
Overlies | Waggoner Ranch Formation |
Thickness | 250 ft (76 m) |
Lithology | |
Primary | Limestone, mudstone |
Other | Gypsum |
Location | |
Coordinates | 33°48′N99°12′W / 33.8°N 99.2°W |
Approximate paleocoordinates | 0°24′N29°36′W / 0.4°N 29.6°W |
Region | Texas |
Country | United States |
Type section | |
Named for | Los Arroyos, Runnels County, Texas |
Named by | Beede & Waithe |
Year defined | 1918 |
The Arroyo Formation, sometimes termed the Lower Clear Fork Formation, is a geologic formation in Texas. [1] It preserves fossils dating back to the Kungurian stage of the Permian period. [2] 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 Arroyo Formation is the oldest and most eastern component of the Clear Fork Group. It extends in a Northeasterly direction from Concho County up as far north as Wilbarger County. North of the Red River in Oklahoma, the equivalent formation is the upper Garber Formation and cave deposits of Richards Spur (formerly Fort Sill). [3] [4]
The Arroyo Formation was first named by Beede and Waite (1918). [5] The type locality was a series of marine limestone, shale, and gypsum deposits cropping out at Los Arroyos (formerly Los Arroyo), a specific arroyo in Runnels County a few miles west of Ballinger. Wrather (1917) observed the same geological sequence in Taylor County, although he named it the Abilene Formation, which was a preoccupied name rejected by Beede and Waite (1918). At first, Beede and Waite (1918) tentatively placed the Arroyo Formation in the Wichita (or Albany) Stage/Group, rather than the overlying Clear Fork Stage/Group. [5] Subsequent authors, starting with Sellars (1932), have considered the Arroyo Formation the basal part of the Clear Fork Group. [6] Olson (1989) called the portion of the Arroyo Formation below the Salt Fork of the Brazos River the "Southern area", contrasting it with the extensively studied "Classic area" further north. [7]
"Southern area" deposits found north of Runnels County preserve a series of terrestrial mudstone layers interspersed with several distinct intervals of marine limestone, four of which having been named. These four limestone intervals are, from stratigraphically lowest to highest, the Rainey, Lytle, Kirby Lake, and Standpipe Limestones. The composition and appearance of these limestones can be variable, with some localities having fine-grained layers and others being practically marine conglomerate. These four limestone layers do not persist in the entirety of the "Southern Area", with the Standpipe Limestone terminating just north of Abilene. This makes it difficult to distinguish the boundary between the Arroyo and Vale Formation north of Taylor County, where it occurs shortly after the top of the Standpipe Limestone. [7]
The limestone layers are often fossiliferous, preserving fossils from both marine organisms and reworked inland fauna. A diverse assortment of palaeoniscoid fish teeth and scales and bivalve shells are by far the most abundant fossils. Worm burrows and ostracods are also very common. Tetrapod remains include Dimetrodon teeth, unusually small " Lysorophus" (Brachydectes) vertebrae, skull fragments from small Diplocaulus and Trimerorhachis , a few Eryops components, and fragments from various microsaurs, possibly referable to Pantylus , Microbrachis , and/or Pelodosotis . Most of the bones belong to small animals, likely due to taphonomic bias due to ease of transportation. This is also a possible reason as for why found teeth from the freshwater lungfish Gnathorhiza, are much smaller and rarer than those from terrestrial deposits. Captorhinus , a common small animal in the "Classic area", is curiously absent. Shark remains include teeth from Orthacanthus and hybodonts. Marine invertebrates mostly belonged to shallow water or estuary niches, apart from a single poorly preserved nautiloid which likely drifted in from more open waters. [7]
Fossils from terrestrial deposits (like stream conglomerate or red mudstone) are rare in the southern area, found at only a handful of sites in Haskell County and southwestern Baylor County. These fossils are probably from a later interval of the Arroyo Formation, a segment which would lie between the Kirby Lake and Standpipe Limestone layers further south. The fauna is similar to that of the "Classic area", with Diplocaulus, Dimetrodon, and Orthacanthus fossils being the most common and Eryops and Diadectes also known, albeit from much more fragmentary remains. [7]
Between the Salt Fork Brazos and Red River, the Arroyo Formation preserves a terrestrial floodplain ecosystem found in outcrops in Baylor, Wilbarger, and Wichita counties. This area, which Olson (1989) termed the "Classic area", has been extensively studied for its Permian plant and animal fossils. [7] The portions of the Arroyo Formation exposed in this area are among the oxidized Permian sediments collectively termed the Red Beds of Texas and Oklahoma. They are represented by Red clays, shales, and mudstones, with occasional layers of sandstone or conglomerate, [8] as well as scattered carbonate nodules which become increasingly more common in younger levels. Some of the sandstone layers have been given informal names, such as the Red Tank and Brushy Creek Sandstone Members. [9] [10] Limestone layers are rare relative to the "southern area", and the diagnostic Taylor County layers are seemingly completely absent north of the Salt Fork, [7] although a dolomite layer possibly equivalent to the Rainey or Lytle limestones has been reported. [9] [10] This dolomite layer, informally named the Craddock dolomite, has been known to preserve plant impressions as well as arthropod and tetrapod footprints. [11]
With the absence of the characteristic Standpipe Limestone of the "southern area", Arroyo red beds in the "classic area" are difficult to differentiate from the overlying Vale Formation on a purely geological basis. A similar issue obscures the boundary between the Vale and Choza Formations, with the absence of the Bullwagon Dolomite which separates the two further south. As a result, sedimentologists generally do not distinguish the component formations of the Clear Fork Group, and simply prefer to call these northern red beds the Clear Fork Formation. [9] Under this system, the Arroyo Formation would be roughly equivalent to the informal "Lower Clear Fork Formation". [10]
Olson (1958) attempted to provide an informal geological boundary between the Arroyo and Vale based on the presence of an even red shale or mudstone layer. This layer is found along a northeastern-oriented line that bisected the Clear Fork area in the western part of Baylor County. This even layer, he argued, was formed by slow, brackish streams in a lowland delta close to sea level. Therefore, their presence may have been a result of the same marine transgression responsible for the Standpipe Limestone further south. Under this hypothesis, the Vale Formation could be found in stratigraphically higher areas west of the line, and the Arroyo formation would be east of the line. Nevertheless, Olson admitted that this boundary was imprecise due to the variable depth of the shales and the varying topography of the surrounding landscape. [12]
The "classic area" of the Arroyo Formation is one of the most fossiliferous parts of the Texas Red Beds, and it is typically differentiated from surrounding formations by paleontologists on the basis of faunal differences. [8] [12] [13] A large number of sites are known bearing either abundant plant or animal remains. The animal-bearing sites are among the most diverse Early Permian tetrapod assemblages in the world, with numerous remains of amphibians, pelycosaurs (mammal relatives), chondrichthyans (sharks), and eureptiles. The last and largest known species of edaphosaurid, Edaphosaurus pogonias , is known from the Arroyo, with the family going extinct soon afterwards. Other pelycosaurs, including Secodontosaurus , Varanosaurus , and several species of Dimetrodon , were abundant, though the abundance of Dimetrodon was retained in the Vale and Choza Formations. Captorhinids were the most common eureptiles in the Arroyo, represented by basal taxa such as Captorhinus and Labidosaurus . [13] [7] Captorhinids experienced a taxonomic turnover at the beginning of the Vale Formation, as advanced taxa like Labidosaurikos and Captorhinikos replace or evolve from the more primitive captorhinids soon after the red shale boundary between the two formations. [12] The first specimens of the gracile eureptile Araeoscelis were discovered at the Craddock Bonebed, one of the most productive Arroyo Formation sites in Baylor County. Aquatic amphibians like Diplocaulus , Trimerorhachis , and Eryops are common. Terrestrial amphibians like Seymouria , Diadectes , microsaurs, and various dissorophoids ( Acheloma , Broiliellus , Aspidosaurus , etc.) were present as well. Many of these terrestrial amphibians did not survive into the Vale Formation. [8] [7] Burrows containing aestivating Brachydectes , Gnathorhiza , and Diplocaulus are common in the middle part of the Arroyo Formation, likely indicating a period with a drier climate than the early or late Arroyo. The most common shark remains belong to Orthacanthus platypternus , although teeth from Xenacanthus luederensis are also known from some early Arroyo sites. [13]
Color key
| Notes Uncertain or tentative taxa are in small text; |
Genus | Species | Notes | Images |
---|---|---|---|
Brachydectes | B. elongatus | A lysorophian common in some sites. Historically referred to Lysorophus tricarinatus . [14] | |
Cardiocephalus | C. sternbergi | A gymnarthrid microsaur [15] | |
Crossotelos | C. annulatus | A urocordylid nectridean. [16] | |
D. brevirostris | Rare [17] | ||
D. copei | Indeterminate, likely a junior synonym of D. magnicornis [17] | ||
D. limbatus | Junior synonym of D. magnicornis [17] | ||
D. magnicornis | An abundant diplocaulid nectridean [17] | ||
D. primigenius | May be synonymous with D. magnicornis [17] | ||
Euryodus | E. primus | A gymnarthrid microsaur [15] | |
G. willistoni | An indeterminate gymnarthrid microsaur known from skull fragments. Initially named Goniocephalus. [15] | ||
Gymnarthrus | G. willoughbyi | Junior synonym of Cardiocephalus sternbergi. [15] | |
Micraroter | M. erythrogeois | An ostodolepid microsaur which may have been present based on BPI 3839, a well-preserved skull and skeleton potentially referable to the genus. [18] | |
Ostodolepis | O. brevispinatus | An ostodolepid microsaur [15] [18] | |
P. coicodus | A fragmentary microsaur. May be synonymous with Pantylus cordatus, or completely unrelated. [15] | ||
Pelodosotis | P. elongatum | An ostodolepid microsaur [18] | |
Permoplatyops | P. parvus | Also known as Diplocaulus pusillus and Platyops parvus. Junior synonym of Diplocaulus magnicornis. [17] | |
Quasicaecilia | Q. texana | A brachystelechid microsaur. Type locality unknown, may be from the Arroyo Formation. [19] |
Genus | Species | Notes | Images |
---|---|---|---|
A. cumminsi | |||
A. willistoni | |||
A. casei | Junior synonym of Isodectes obtusus [20] | ||
A. aphthitos | Junior synonym of Aspidosaurus chiton [21] | ||
A. chiton | A dissorophid | ||
A. peltatus | Junior synonym of Dissorophus multicinctus | ||
Broiliellus | B. arroyoensis | A dissorophid [22] | |
Cacops | C. aspidephorus | A dissorophid | |
Dasyceps | D. micropthalmus | A zatrachydid [23] | |
Dissorophus | D. multicinctus | A dissorophid | |
E. townendae | Junior synonym of Isodectes obtusus [20] | ||
Eryops | E. megacephalus | A common eryopid | |
I. obtusus | A dvinosaur [20] | ||
I. megalops | Junior synonym of Isodectes obtusus [20] | ||
Kermitops [24] | K. gratus [24] | An amphibamiform [24] | |
Nanobamus | N. macrorhinus | An amphibamiform [25] | |
T. insignis | A common dvinosaur [26] | ||
T. mesops | Rare [26] | ||
T. conangulus | Junior synonym of Isodectes obtusus [20] | ||
T. greggi | May be descended from T. insignis [26] |
Genus | Species | Notes | Images |
---|---|---|---|
Desmospondylus | D. anomalus | Junior synonym of Seymouria baylorensis | |
Seymouria | S. baylorensis |
Genus | Species | Notes | Images |
---|---|---|---|
Diadectes | D. tenuitectens | A diadectid |
Genus | Species | Notes | Images |
---|---|---|---|
Casea | C. broilii | A caseid | |
Dimetrodon | D. giganhomogenes | A sphenacodontid | |
D. grandis | |||
D. kempae | Dubious | ||
D. loomisi | A sphenacodontid | ||
Edaphosaurus | E. pogonias | An edaphosaurid | |
Secodontosaurus | S. obtusidens | A sphenacodontid | |
Tetraceratops | T. insignis | An advanced pelycosaur or early therapsid | |
Trichasaurus | T. texensis | A caseid | |
Varanops | V. brevirostris | A varanopid | |
Varanosaurus | V. acutirostris | An ophiacodontid | |
Genus | Species | Notes | Images |
---|---|---|---|
Araeoscelis | A. grandis | An araeoscelidian diapsid | |
Captorhinus | C. aguti | A captorhinid | |
Ectocynodon | E. incisivus | Junior synonym of Captorhinus aguti. Has also been referred to the microsaur Pariotichus and the captorhinid Labidosaurus . | |
Labidosaurus | A. hamatus | A captorhinid | |
Apart from sharks and lungfish, a large and well-preserved actinopterygian fish, Brachydegma caelatum , is known from the lower Clear Fork Formation. [27]
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.
Lepospondyli is a diverse taxon of early tetrapods. With the exception of one late-surviving lepospondyl from the Late Permian of Morocco, lepospondyls lived from the Early Carboniferous (Mississippian) to the Early Permian and were geographically restricted to what is now Europe and North America. Five major groups of lepospondyls are known: Adelospondyli; Aïstopoda; Lysorophia; Microsauria; and Nectridea. Lepospondyls have a diverse range of body forms and include species with newt-like, eel- or snake-like, and lizard-like forms. Various species were aquatic, semiaquatic, or terrestrial. None were large, and they are assumed to have lived in specialized ecological niches not taken by the more numerous temnospondyl amphibians that coexisted with them in the Paleozoic. Lepospondyli was named in 1888 by Karl Alfred von Zittel, who coined the name to include some tetrapods from the Paleozoic that shared some specific characteristics in the notochord and teeth. Lepospondyls have sometimes been considered to be either related or ancestral to modern amphibians or to Amniota. It has been suggested that the grouping is polyphyletic, with aïstopods being primitive stem-tetrapods, while recumbirostran microsaurs are primitive reptiles.
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.
Ctenospondylus is an extinct genus of sphenacodontid synapsid
Secodontosaurus is an extinct genus of "pelycosaur" synapsids that lived from between about 285 to 272 million years ago during the Early Permian. Like the well known Dimetrodon, Secodontosaurus is a carnivorous member of the Eupelycosauria family Sphenacodontidae and has a similar tall dorsal sail. However, its skull is long, low, and narrow, with slender jaws that have teeth that are very similar in size and shape—unlike the shorter, deep skull of Dimetrodon, which has large, prominent canine-like teeth in front and smaller slicing teeth further back in its jaws. Its unusual long, narrow jaws suggest that Secodontosaurus may have been specialized for catching fish or for hunting prey that lived or hid in burrows or crevices. Although no complete skeletons are currently known, Secodontosaurus likely ranged from about 2 to 2.7 metres (7–9 ft) in length, weighing up to 110 kilograms (250 lb).
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.
Diplocaulus is an extinct genus of lepospondyl amphibians which lived from the Late Carboniferous to the Late Permian of North America and Africa. Diplocaulus is by far the largest and best-known of the lepospondyls, characterized by a distinctive boomerang-shaped skull. Remains attributed to Diplocaulus have been found from the Late Permian of Morocco and represent the youngest-known occurrence of a lepospondyl.
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.
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.
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.
Trimerorhachis is an extinct genus of dvinosaurian temnospondyl within the family Trimerorhachidae. It is known from the Early Permian of the southwestern United States, with most fossil specimens having been found in the Texas Red Beds. The type species of Trimerorhachis, T. insignis, was named by American paleontologist Edward Drinker Cope in 1878. Cope named a second species from Texas, T. mesops, in 1896. The species T. rogersi and T. greggi are also from Texas, and the species T. sandovalensis is from New Mexico.
The Tambach Formation is an Early Permian-age geologic formation in central Germany. It consists of red to brown-colored sedimentary rocks such as conglomerate, sandstone, and mudstone, and is the oldest portion of the Upper Rotliegend within the Thuringian Forest Basin.
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.
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 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 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 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.
The Nocona Formation is a geological formation in Texas, dating back to the Wolfcampian series. As part of the Texas red beds, it is one of several formations renowned for dense bonebeds of terrestrial vertebrate fossils.
The Organ Rock Formation or Organ Rock Shale is a formation within the late Pennsylvanian to early Permian Cutler Group and is deposited across southeastern Utah, northwestern New Mexico, and northeastern Arizona. This formation notably outcrops around Canyonlands National Park, Natural Bridges National Monument, and Monument Valley of northeast Arizona, southern Utah. The age of the Organ Rock is constrained to the latter half of the Cisuralian epoch by age dates from overlying and underlying formations. Important early terrestrial vertebrate fossils have been recovered from this formation in northern Arizona, southern Utah, and northern New Mexico. These include the iconic Permian terrestrial fauna: Seymouria, Diadectes, Ophiacodon, and Dimetrodon. The fossil assemblage present suggests arid environmental conditions. This is corroborated with paleoclimate data indicative of global drying throughout the early Permian.
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.