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Permian

The Permian is a geologic period and the final division of the Paleozoic Era, extending from 298.9 ± 0.15 Ma to 251.902 ± 0.024 Ma (47 million years in duration).^[1] It is defined by the consolidation of the supercontinent Pangaea, which encompassed nearly all of Earth's landmasses and was surrounded by the vast Panthalassa ocean, with the Palaeotethys as a prominent gulf.^[2]^[1] During the Permian, global climates shifted from an icehouse state at its onset to increasingly arid conditions, fostering vast interior deserts within Pangaea while supporting tropical forests near the equator and polar glaciation.^[2] The period is subdivided into three series—the Cisuralian (early Permian), Guadalupian (middle), and Lopingian (late)—further divided into nine stages, providing a framework for global stratigraphic correlation.^[1] Paleogeographically, the assembly of Pangaea influenced ocean circulation, leading to reduced shallow marine habitats compared to earlier Paleozoic times and promoting the diversification of terrestrial ecosystems.^[2]^[1] Life during the Permian was remarkably diverse, with marine realms dominated by brachiopods, fusulinid foraminifers, conodonts, ammonoids, and reef-building sponges, while terrestrial environments saw the rise of synapsids (precursors to mammals), archosauromorphs, and conifer-dominated forests replacing Carboniferous coal swamps.^[1]^[2] Amphibians declined as habitats dried, and insects proliferated in the changing landscapes.^[2] The period ended catastrophically with the Permian-Triassic mass extinction around 252 Ma, the most severe in Earth's history, eradicating approximately 96% of marine species and 70% of terrestrial vertebrate genera, likely triggered by massive Siberian Traps volcanism, methane release, and anoxic oceans.^[2]^[1] This event marked the transition to the Mesozoic Era, profoundly reshaping global biodiversity.^[2]

Etymology and history

Name origin

The term "Permian" was coined in 1841 by Scottish geologist Sir Roderick Impey Murchison during his fieldwork in European Russia, named after the Perm Governorate (modern-day Perm Krai), a region in the western Ural Mountains where these strata form extensive outcrops and served as the type locality for the system.^[3] Murchison selected the name to honor the ancient kingdom of Permia, emphasizing the deposits' prominence in this area as a means to establish a globally applicable stratigraphic unit.^[4] Murchison proposed "Permian" specifically to delineate a rock sequence that overlies Carboniferous strata and underlies Triassic beds, distinguished by its red sandstones, marls, limestones, gypsums, and transitional fossil assemblages—such as Productus species—that bridged Paleozoic and Mesozoic faunas, avoiding conflation with the coal-rich, marine-dominated Carboniferous below.^[3] This nomenclature filled a gap in the emerging Paleozoic timescale, completing the major systems from Cambrian to Permian as recognized in Britain and Europe.^[5] Early adoption faced challenges due to discrepancies between Murchison's Permian and preexisting Russian stratigraphic nomenclature, including the Uralian series for lower Permian equivalents, which led to inconsistencies in correlations across the Russian platform and Urals among local geologists.^[6] By the 1870s, however, the term "Permian" gained widespread international acceptance, supplanting alternatives like the German "Dyas" and becoming standardized in global geological usage following detailed mappings in Russia and Europe.^[7] The regional name "Perm" derives from the Old Permic (Komi-Permyak) language, where it relates to parma, meaning a forested hill or ridge covered in dense woodland, evoking the taiga-dominated landscape of the area inhabited by Permic peoples.^[8]

Discovery and early research

The initial mapping of strata in the Perm region of Russia during the early 19th century laid foundational work for recognizing what would later be defined as Permian rocks. Karl Eichwald, a Baltic-German geologist and paleontologist, advanced the understanding of Russian Paleozoic sequences through his systematic descriptions of fossils from the Baltic provinces and around St. Petersburg, introducing modern paleontological methods to the region and identifying key stratigraphic units that included post-Carboniferous layers.^[3] His 1840 publication on ancient life in the region highlighted distinctive faunas that distinguished these strata from underlying Carboniferous deposits.^[9] Complementing this, Alexander Keyserling, a German-Russian count and geologist trained in Berlin, conducted extensive surveys across European Russia, documenting sedimentary successions in the Perm area and northern regions like the Pechora Basin; his observations on rock types, fossils, and structural features contributed to early regional stratigraphic frameworks.^[3]^[10] The pivotal moment in the discovery of the Permian came in 1841 through Roderick Murchison's expedition to the Ural Mountains, funded by Tsar Nicholas I and undertaken with collaborators Édouard de Verneuil and Keyserling. Traversing over 4,000 miles of terrain, Murchison examined rock sequences overlying Carboniferous limestones and underlying Triassic beds, first encountering characteristic red sandstones and gypsum at Vyazniki, which he recognized as a distinct unit.^[11] In a letter dated October 8, 1841, published in the Bulletin de la Société Impériale des Naturalistes de Moscou, he formally named this interval the "Permian System" after the Perm province, emphasizing its paleontological (e.g., Productus cancrini shells), lithological (e.g., magnesian limestones), and geographical continuity.^[3] This culminated in the comprehensive two-volume publication The Geology of Russia in Europe and the Ural Mountains (1845), co-authored with de Verneuil and Keyserling, which included detailed maps, sections, and fossil illustrations establishing the Permian as a global stratigraphic entity equivalent to the German Zechstein and British Magnesian Limestone.^[9]^[12] Murchison's proposal ignited significant debates among geologists, particularly regarding the Permian's lower boundary with the Carboniferous and its distinction from Triassic rocks. Adam Sedgwick, a prominent British geologist, contested Murchison's inclusion of the Magnesian Limestone (now recognized as basal Permian) within the Paleozoic, arguing it belonged to the Triassic based on its evaporitic and red-bed characteristics in northeastern England, while Murchison insisted on its faunal and stratigraphic continuity with underlying Carboniferous sequences.^[13] These disputes, extending to equivalences with continental "Dyas" formations proposed by Jules Marcou in 1859, delayed widespread acceptance of the Permian as a separate system until international consensus. The boundary issues were formally resolved at the 1878 International Geological Congress in Paris, where delegates affirmed the Permian above the Carboniferous based on fossil evidence and stratigraphic superposition, solidifying its position in the global timescale.^[13]^[14] Twentieth-century research refined the Permian's internal divisions through international collaboration, culminating in significant standardization during the 18th International Geological Congress in Great Britain in 1948, which advanced chronostratigraphic units based on integrated biostratigraphy and lithostratigraphy from type regions in Russia and the Americas.^[14] Early correlations relied heavily on fossil assemblages, with fusulinid foraminifera serving as primary index fossils for marine sequences due to their rapid evolution and wide distribution, enabling precise zoning from the Asselian to the Changhsingian.^[15] Brachiopods, particularly spiriferids and productids, complemented these efforts by providing robust markers for shelf environments and facilitating interregional ties, such as linking Eurasian and North American successions through shared genera like Productus and Spirifer.^[16] These biotic tools were instrumental in delineating the period's subdivisions without reliance on radiometric dating at the time.

Geological framework

Cisuralian Epoch

The Cisuralian Epoch represents the lower series of the Permian System, spanning from approximately 298.9 to 272.3 million years ago, and is named for the Cis-Ural region on the western slopes of the Ural Mountains in Russia and Kazakhstan, where its type strata are exposed.^[17]^[18] This epoch marks the initial phase of the Permian Period, transitioning from the late Carboniferous icehouse conditions toward more stable continental configurations.^[19] The Cisuralian is subdivided into four global stages: the Asselian at the base (298.9–293.52 Ma), followed by the Sakmarian (293.52–290.1 Ma), Artinskian (290.1–283.5 Ma), and Kungurian (283.5–272.3 Ma).^[18] The Asselian-Sakmarian boundary is placed at 293.52 ± 0.17 Ma, with the base of the Sakmarian Stage defined at the Usolka section, Russia, by the first appearance of the conodont Sweetognathus binodosus.^[20] These stages reflect a period of gradual climatic warming and tectonic stabilization following the Carboniferous glaciation. Tectonically, the Cisuralian witnessed the final assembly of the supercontinent Pangea, driven primarily by the waning phases of the Variscan and Uralian orogenies.^[21]^[22] The Variscan orogeny involved the collision between Gondwana and Laurussia (Euramerica), forming extensive mountain belts across southern Europe and North America, while the Uralian orogeny resulted from the closure of the Ural Ocean between Laurussia and Kazakhstania, extending deformation into eastern Europe.^[21]^[22] These events contributed to the consolidation of Pangea, promoting widespread subsidence and the development of coal-forming swamps in humid, low-lying basins across Euramerica and northern Gondwana, where glossopterid floras dominated peat accumulation.^[23]^[24] Dominant lithologies during the Cisuralian vary by paleogeographic region, reflecting diverse depositional environments amid ongoing deglaciation and tectonic activity. In southern Gondwana, glacial and post-glacial deposits, such as the diamictites and tillites of the Dwyka Group in South Africa, record the final stages of the late Paleozoic ice age, overlain by terrestrial red beds and coal measures.^[25] Along the northern margins of Gondwana and in the Paleo-Tethys realm, extensive carbonate platforms developed, including shallow-marine limestones and reefs that hosted diverse benthic communities.^[19] In contrast, northern continents like Euramerica featured red beds—predominantly sandstones and shales with oxidized iron content—deposited in fluvial and alluvial settings, indicative of arid to semi-arid conditions in interior basins.^[26] Biostratigraphically, the Cisuralian is characterized by key marine and terrestrial markers that facilitate global correlation. Primitive conodonts of the genus Streptognathodus, such as S. wabaunsensis, define the base of the Asselian and persist into the Sakmarian, marking the transition from Carboniferous faunas with their distinctive barred apparatus elements abundant in open-marine carbonates.^[27] On land, the appearance of early therapsids—synapsid amniotes including basal forms like Biarmosuchus—in upper Cisuralian deposits of Euramerica and Gondwana signals the diversification of mammal-like reptiles, often associated with tetrapod assemblages in red bed sequences.^[28] These markers, combined with fusulinids and ammonoids, underpin the epoch's chronostratigraphic framework.^[29]

Guadalupian Epoch

The Guadalupian Epoch, the middle subdivision of the Permian Period, spans from 272.95 ± 0.11 Ma to 259.51 ± 0.21 Ma.^[18] It is divided into three stages: the Roadian (272.95 ± 0.11 Ma to 266.9 ± 0.4 Ma), Wordian (266.9 ± 0.4 Ma to 264.28 ± 0.16 Ma), and Capitanian (264.28 ± 0.16 Ma to 259.51 ± 0.21 Ma).^[18] The epoch is named for the Guadalupe Mountains in western Texas and southeastern New Mexico, where key exposures of its strata occur.^[30] Its lower boundary is defined by the first appearance of the conodont Jinogondolella nankingensis at the GSSP in Stratotype Canyon, Guadalupe Mountains, Texas, while the upper boundary is marked by the first occurrence of the conodont Jinogondolella postserrata.^[31]^[32] Within the Guadalupian, conodont zones such as the Jinogondolella nankingensis Zone characterize early Roadian assemblages, providing precise biostratigraphic correlation across regions.^[33] During the Guadalupian, the supercontinent Pangea achieved relative tectonic stability following the final assembly phases of the Uralian orogeny, which concluded in the latest Cisuralian.^[34] This stability fostered the development of extensive interior cratonic basins and marginal epicontinental seas, with reduced tectonic activity allowing for widespread subsidence and sedimentation across the supercontinent.^[35] Sedimentary records reflect this setting, including thick evaporite sequences in restricted basins; for example, the Zechstein Basin in northern Europe accumulated cyclic evaporites during the late Guadalupian, driven by arid conditions and sea-level fluctuations.^[36] In North America, the Palo Duro Basin preserved Guadalupian evaporites, such as those in the Seven Rivers Formation, indicative of hypersaline lagoonal environments.^[36] Prominent reef complexes also formed along basin margins, exemplified by the Capitan Reef in the Delaware Basin of Texas and New Mexico, a massive carbonate buildup dominated by sponges, algae, and bryozoans that reached up to 1,000 meters in thickness.^[37] Biostratigraphically, the Guadalupian represents the peak of fusulinid foraminiferan diversity, with genera such as Parafusulina achieving high abundance and morphological complexity in shallow-marine carbonates worldwide. This diversification reflects optimal warm, shallow-water conditions before a gradual decline toward the epoch's end.^[38] Concurrently, Carboniferous holdover flora, including lycopods and seed ferns, continued to wane as gymnosperm-dominated assemblages expanded in terrestrial settings.^[39] A transitional warming trend during the epoch contributed to these biotic shifts, enhancing evaporation in marginal seas.^[35]

Lopingian Epoch

The Lopingian Epoch represents the final division of the Permian Period, spanning from 259.51 ± 0.21 Ma to 251.902 ± 0.024 Ma, and is divided into two stages: the Wuchiapingian (259.51 ± 0.21 to 254.14 ± 0.07 Ma) and the Changhsingian (254.14 ± 0.07 to 251.902 ± 0.024 Ma).^[40] The name derives from Loping (now Leping), a town in Jiangxi Province, China, where characteristic coal-bearing series were first identified in the late 19th century. This epoch marks a period of relative stability in the supercontinent Pangea, which had reached its final configuration by the late Permian, with equatorial latitudes dominated by vast arid interiors.^[41] During the Lopingian, tectonic activity intensified along the margins of Pangea, characterized by compressional regimes associated with subduction zones and continental collisions. In eastern Asia, the initiation of the Indosinian orogeny began in the late Permian, driven by the northward drift and collision of the Indochina block with the South China block, leading to uplift and basin inversion.^[42] Sedimentary records reflect these dynamics, with widespread red beds and playa lake deposits in the western regions of Pangea, such as the southwestern United States, indicating arid to semi-arid continental environments with episodic fluvial and evaporitic sedimentation.^[43] In contrast, the Panthalassa Ocean featured deep-water bedded cherts, formed from siliceous biogenic oozes in pelagic settings below the carbonate compensation depth, preserving evidence of radiolarian productivity amid expanding anoxic conditions toward the epoch's close.^[44] Biostratigraphically, the Lopingian is marked by significant faunal shifts, including a progressive decline in Paleozoic ammonoid orders such as Goniatitida and Prolecanitida, culminating in their near-extinction by the Changhsingian, while ceratitid ammonoids began to emerge.^[45] The ammonoid genus Otoceras appears abruptly at the epoch's end, serving as a key marker for the Permian-Triassic transition. Concurrently, dicynodont therapsids underwent a notable radiation, achieving peak diversity with around 20 genera by the late Lopingian, dominating herbivorous niches across Pangea's southern high latitudes.^[46] The upper boundary of the Lopingian Epoch, defining the Permian-Triassic boundary, is formally recognized at the Global Stratotype Section and Point (GSSP) in the Meishan section, Zhejiang Province, China, based on the first appearance of the conodont Hindeodus parvus.^[47] Geochemical signatures at this boundary include hints of an iridium anomaly, with concentrations up to several parts per billion in boundary clays, suggesting possible extraterrestrial influence amid broader environmental perturbations.^[48]

Regional chronostratigraphy

The regional chronostratigraphy of the Permian Period exhibits significant variations across continents due to local tectonic settings, sedimentary environments, and historical naming conventions, necessitating biostratigraphic correlations for global integration. In North America, particularly in the Permian Basin of Texas and New Mexico, the system is divided into four series: the Wolfcampian and Leonardian (both Cisuralian), Guadalupian (middle Permian), and Ochoan (Lopingian equivalent). The Leonardian Stage, spanning approximately 290–280 Ma, corresponds to the early Cisuralian and is characterized by marine carbonates and clastics in the Glass Mountains region, while the Guadalupian, from about 272–259 Ma, includes reefal limestones and evaporites in the Guadalupe Mountains. The Ochoan, roughly 259–252 Ma, represents the late Permian with predominantly evaporitic deposits like the Castile Formation. These North American stages were formalized based on fossil assemblages and lithostratigraphy in the mid-20th century.^[49] In Europe, Permian chronostratigraphy reflects a continental to marginal marine succession, with the Rotliegendes Group encompassing the Cisuralian red beds and volcanics deposited in rift basins across northwest Europe, dated to around 299–272 Ma. The Zechstein Group, overlying the Rotliegendes, comprises Guadalupian to Lopingian evaporites, carbonates, and shales formed in a restricted sea, spanning approximately 259–252 Ma and reaching thicknesses up to 2,000 m in northern Germany. Older European nomenclature includes the Saxonian (early to mid-Permian continental deposits) and Thuringian (late Permian red beds and evaporites) stages, which broadly align with the Autunian-Saxonian-Thuringian triad but have been largely superseded by global series for precise correlation. These divisions stem from 19th-century mappings in the Thuringian Forest and Saxony regions. Gondwanan Permian sequences, such as the Karoo Supergroup in South Africa, feature lithostratigraphic units rather than formal stages, with the Ecca Group representing Cisuralian marine to deltaic shales and sandstones deposited from about 299–280 Ma in a foreland basin setting. The overlying Beaufort Group encompasses Guadalupian to Lopingian fluvial and terrestrial red beds, spanning 280–252 Ma, with vertebrate fossils aiding age assignments. Correlations to the global scale rely on palynomorphs and glossopterid floras, linking the Ecca to the Artinskian-Sakmarian stages. These units reflect the Late Paleozoic Ice Age's influence on southern high latitudes.^[50] In Asia, the Salt Range of Pakistan preserves a Permian succession with local formations like the Tobra (early Cisuralian glacial-marine, ~299–290 Ma), Warchha Sandstone (Artinskian fluvial-marine, ~290–280 Ma), and Zaluch Group (Guadalupian-Lopingian carbonates and shales, ~272–252 Ma), where boundary debates arise from potential Visean (late Carboniferous) influences in basal clastics due to glacial erratics. The Chhidru Formation, for instance, hosts Kungurian-Wordian ammonoids, facilitating ties to Tethyan realms. These Asian variants highlight peri-Gondwanan marine incursions.^[51] Inter-regional correlations face challenges from facies differences, such as continental red beds in Europe and Gondwana versus marine sections in North America and Asia, but are resolved using index fossils like the ammonoid genus Waagenoceras, which defines the Wordian Stage (Guadalupian) and appears in Tethyan and North American basins for transcontinental matching. Ammonoid zonations, supplemented by conodonts and fusulinids, enable precise alignment despite local tectonic disruptions.^[52]

Paleogeography

Continental configurations

The assembly of the supercontinent Pangea was largely complete by the late Cisuralian Epoch through the collision of the major continental blocks Laurussia, Gondwana, and Angara, driven primarily by the Hercynian-Appalachian and Uralian orogenies.^[53] The Hercynian-Appalachian orogeny arose from the closure of the Rheic Ocean basin, leading to the convergence of Laurussia and Gondwana beginning in the Late Devonian and culminating in the Early Permian. This tectonic event produced extensive deformational belts across the proto-Atlantic region. Meanwhile, the Uralian orogeny, active from the Middle Carboniferous through the Early Permian, marked the suturing of Angara (the Siberian craton) to the eastern margin of Laurussia, finalizing the core structure of Pangea around 290–280 Ma.^[22] In the late Permian, Pangea assumed a near-equatorial orientation, extending from high southern to high northern latitudes with a narrow Paleotethys seaway along its eastern flank that constrained intercontinental connectivity.^[53] By this time, additional accretions had integrated Kazakhstania and Siberia into the northern framework via ongoing Central Asian and Uralian tectonics, stabilizing the supercontinent's configuration.^[22] Paleomagnetic data indicate Gondwana positioned at high southern latitudes (approximately 40–50°S in the early Permian), while northern landmasses like Laurussia occupied subtropical zones around 20–30°N.^[54] Prominent mountain belts shaped Pangea's topography, including the Variscan ranges across Europe, formed during the Hercynian phase, and the Ouachita belt in southern North America, a southern extension of the Appalachian system. These orogenic features directed continental drainage, with major fluvial systems originating from the elevated margins and flowing inward toward Pangea's arid heartland, fostering expansive sabkha depositional environments characterized by evaporitic sediments in closed basins.^[55]

Ocean basins and paleoceanography

During the Permian Period, the global ocean system was dominated by Panthalassa, a vast superocean that encircled the supercontinent Pangea, dominating the global ocean system and comprising approximately 85-90% of its total area, featuring extensive subduction zones along its western margins adjacent to Laurussia and Gondwana.^[56] These subduction zones facilitated the recycling of oceanic crust and drove volcanic arc development, contributing to the dynamic evolution of the Circum-Panthalassa region. Panthalassa's bathymetry included a prominent mid-ocean ridge system with crest depths around 2,800 meters, supporting moderate seafloor spreading rates of about 10 cm/year, which influenced overall ocean depth averaging 4 km.^[57] The Tethys Ocean, positioned between northern and southern landmasses, comprised the Paleo-Tethys to the north and the emerging Neo-Tethys arm to the south, which began rifting in the Early Permian and expanded to connect equatorial regions with higher latitudes, enabling enhanced warm-water exchange.^[58] Shallow sills, estimated at 200 meters depth, separated the Paleo-Tethys from Panthalassa, restricting deep-water flow and promoting stratified conditions in the Tethyan basins.^[57] Basin configurations included active convergent margins with volcanic arcs along the eastern Gondwana front facing Panthalassa, where subduction of oceanic lithosphere generated island arcs and back-arc basins, contrasting with more stable passive margin settings in parts of eastern Gondwana's interior transitions.^[59] Seafloor spreading rates in Panthalassa appear to have been relatively subdued during the mid-Permian compared to later Mesozoic pulses, limiting the renewal of deep ocean waters and contributing to gradual basin isolation.^[60] Ocean circulation in Panthalassa was characterized by robust subtropical gyres centered around 30° latitude, reaching strengths up to 60 Sverdrups—roughly twice that of the modern South Pacific—driven by trade winds across Pangea, which induced zonal flow and equatorial divergence.^[61] Equatorial upwelling zones in eastern Panthalassa supported nutrient-rich surface waters with velocities exceeding 1 × 10⁻⁶ m/s, while poleward heat transport via western boundary currents warmed high latitudes, fostering warm polar inflows through open seaways.^[61] The Tethys connection amplified a warm equatorial pool extending poleward, but by the late Permian, Pangea-induced restrictions on circumequatorial currents, combined with sill barriers, slowed deep circulation—evidenced by increased water residence times up to 3,100 years below 3,300 meters—and initiated widespread anoxic conditions in restricted basins like the Paleo-Tethys, where oxygen levels dropped below 20 µmol/L in deeper waters.^[57]

Climate

Cisuralian climate

The Cisuralian Epoch marked the waning of the Karoo Ice Age, with glacial retreat in Gondwana largely completing by the Sakmarian Stage. Evidence from the Dwyka Group in southern Africa shows the final deglaciation sequence terminating at the end of the Sakmarian in shelf facies, transitioning from diamictites and tillites to post-glacial fluvial and lacustrine deposits.^[62] This shift is documented across Gondwanan basins, where glacial sediments give way to coal measures indicative of warmer, wetter conditions supporting peat accumulation in swamps.^[63] In Euramerica, the climate was predominantly humid and temperate, featuring extensive swampy floodplains that fostered coal-forming environments. These conditions supported lush vegetation in low-lying areas, with floral assemblages reflecting moist habitats. Oxygen isotope data from brachiopod shells (δ¹⁸O) reveal relatively high values in the Asselian Stage, pointing to cooler polar temperatures that moderated global gradients during this transitional period.^[64] A subsequent δ¹⁸O decline into the Sakmarian-Artinskian indicates gradual warming, consistent with the icehouse-to-greenhouse transition.^[64] Precipitation patterns during the Cisuralian were influenced by emerging monsoonal circulation linked to the early assembly of Pangea, resulting in seasonal river systems that deposited cyclothems and supported episodic flooding. Climate models simulate a strong southern monsoon in the Sakmarian, driving wetter conditions in southern landmasses, while northern monsoons were weaker but still contributed to seasonal variability in precipitation across equatorial regions.^[65] Atmospheric CO₂ levels hovered around 300-400 ppm, rising from Carboniferous lows of approximately 180 ppm, as reconstructed from soil carbonates and fossil leaf stomata, facilitating the post-glacial recovery.^[66] Proxy evidence from plant fossils underscores the prevalence of wetter climates, with lycopods dominating assemblages in coal swamps and floodplain deposits, reflecting adaptation to humid, low-energy environments. These arborescent lycopods, such as those in the Lepidodendrales, formed dense forests in temperate zones, their distribution correlating with coal occurrences and indicating sustained moisture availability.^[23]

Guadalupian and Lopingian climate

The Guadalupian and Lopingian epochs marked a progressive shift toward warmer and drier global conditions across Pangea, transitioning from a relatively humid early Permian state to a pronounced greenhouse climate that intensified environmental stress leading into the end-Permian crisis. Atmospheric CO₂ levels rose during the Guadalupian, reaching approximately 1000–2000 ppm based on stomatal proxies, driven primarily by volcanic emissions from the Emeishan Large Igneous Province (LIP).^[67]^[68] This CO₂ increase contributed to global warming, promoting evaporite precipitation in interior basins such as the Delaware Basin, where restricted circulation and heightened evaporation led to widespread deposition of gypsum and halite under arid conditions.^[69] In the Lopingian, climate extremes intensified, with hyper-arid conditions dominating Pangea's continental interiors, where mean annual temperatures approached 40°C and seasonal highs reached 45–50°C, as evidenced by paleosol and sedimentary records from the Moradi Formation in central Pangea.^[70] Along Pangea's coastal margins, a megamonsoonal circulation pattern developed, driven by the supercontinent's configuration and thermal contrasts, resulting in intensified seasonal rainfall and fluvial activity near the Tethys and Panthalassa margins.^[71] CO₂ levels stabilized at 500–1000 ppm, sustaining elevated temperatures without polar ice sheets by the Wordian stage of the Guadalupian epoch.^[67]^[72] Paleosol evidence underscores this aridification trend, with widespread calcrete development in continental sequences indicating prolonged dry seasons and episodic precipitation, as seen in North American and European sections.^[73] Concurrent δ¹³C excursions in pedogenic carbonates, with negative shifts exceeding -5‰ across the Guadalupian–Lopingian boundary, reflect perturbations in the global carbon cycle, likely tied to enhanced weathering and organic matter input under fluctuating moisture regimes.^[74]^[75] Regionally, these changes manifested in the contraction of humid equatorial zones, where rainforests declined sharply in western Pangea due to rising aridity and CO₂-driven physiological stress on glossopterid-dominated flora.^[76] Polar regions transitioned to ice-free conditions by the Wordian, supporting temperate forests but experiencing increased seasonality.^[72] Ocean-atmosphere interactions amplified these trends, with restricted basins like the Delaware and Sverdrup experiencing elevated salinities from evaporative drawdown, fostering localized anoxia as a precursor to broader marine deoxygenation.^[77]^[78] Late-stage volcanic activity further exacerbated these imbalances, contributing to carbon cycle disruptions at the epoch's end.^[79]

Biota

Flora

During the Cisuralian epoch, Permian flora was characterized by extensive wetland ecosystems dominated by arborescent lycopods such as Lepidodendron and Sigillaria, alongside calamitaleans like Calamites, which thrived in swampy, peat-forming habitats across Euramerica and other tropical regions.^[80] These plants, adapted to high-moisture environments, formed dense coal forests that supported significant organic carbon burial. In Gondwana, glossopterids emerged as dominant elements in lowland assemblages, rapidly colonizing habitats vacated by earlier vegetation following deglaciation, with Glossopteris forming arborescent stands indicative of cooler, seasonal climates.^[81] This distribution reflected a global pattern where Euramerican floras emphasized wetland pteridophytes and sphenopsids, while Gondwanan assemblages featured seed-bearing glossopterids adapted to higher southern latitudes.^[23] A marked shift occurred from the Guadalupian to Lopingian epochs, driven by progressive aridification and wetland decline, leading to the expansion of drier upland vegetation dominated by seed plants.^[82] Conifers, particularly walchian forms like Walchia, rose in prominence within these seasonally dry landscapes, forming low-diversity forests on well-drained substrates in Euramerica and adjacent regions.^[83] Ginkgophytes also proliferated in these environments, contributing to the transition toward gymnosperm-dominated biomes better suited to reduced precipitation.^[82] Seed ferns, exemplified by taxa related to Neuropteris, faded in abundance as spore-producing groups waned, supplanted by more drought-tolerant seed plants amid the overall vegetational restructuring.^[84] Cathaysian floras of eastern Asia featured distinctive gigantopterids, large-leaved seed ferns interpreted as climbing vines or lianas that added structural complexity to tropical woodlands during the late Permian.^[23] Globally, Euramerican assemblages contrasted with Gondwanan ones through the prevalence of callipterids like Callipteris in arid zones, signaling adaptation to semi-arid conditions with sparse, conifer-rich vegetation.^[85] This biogeographic partitioning underscored the influence of paleoclimate, with mixed floras occurring along transitional margins.^[23] Ecologically, the Permian progression from expansive coal swamps to drier ecosystems reduced carbon sequestration via diminished peat accumulation, contributing to atmospheric CO2 accumulation and the termination of the Late Paleozoic Ice Age.^[86] The decline in wetland flora, particularly lycopod-dominated forests, lessened organic matter burial rates, amplifying greenhouse effects that facilitated the rise of seed plant hegemony.

Marine biota

The marine biota of the Permian period exhibited remarkable diversity, particularly in tropical and subtropical shallow-water environments, where invertebrates dominated reef and shelf ecosystems. Foraminifera, especially the fusulinids, achieved their zenith of morphological and taxonomic diversity during this era, with genera such as Schwagerina exemplifying the group's adaptation to carbonate platforms; these single-celled organisms developed elongated, rice-like tests reaching up to 1 cm in length, facilitated by elevated atmospheric oxygen levels that enabled gigantism.^[87] Brachiopods, another key component of benthic communities, saw the order Productida emerge as the most abundant and morphologically varied group throughout the Permian, comprising species with robust, spinose shells that anchored in soft sediments and contributed to bioclastic deposits.^[88]^[89] Rugose corals, though less dominant than in earlier Paleozoic times, played a significant role in constructing frameworks within Permian reefs, forming colonial structures alongside other organisms in warm, clear waters of the Tethys Ocean.^[90]^[91] Mollusks and echinoderms further enriched Permian marine ecosystems, with nautiloids representing the era's most prominent cephalopods in the expansive Tethys seaway, where their straight or coiled shells supported active swimmers in open marine settings.^[92] Crinoids, stalked echinoderms, proliferated in the Tethys region, forming dense "crinoid gardens" on seafloors and contributing biogenic carbonates to sedimentary layers through their calyxes and arms. Ammonoids, evolving from simpler goniatite ancestors with straight sutures, developed more intricate ceratite patterns during the Permian, reflecting adaptive radiations in pelagic habitats and serving as key index fossils for biostratigraphy.^[93]^[94] Vertebrate components included chondrichthyans such as the enigmatic shark-like Helicoprion, characterized by a unique whorl of fused teeth embedded in the lower jaw, which functioned to slice through soft-bodied prey in coastal waters; this eugeneodontid thrived across Permian oceans, with estimates based on tooth whorls suggesting a body length of 5-8 meters (16-26 feet).^[95] Actinopterygians, or ray-finned fishes, inhabited shallow marine realms, where their diverse forms—ranging from small schooling species to larger predators—filled niches in lagoons and nearshore environments, often preserved in lagerstätten like those of the Phosphoria Formation.^[96] Ecological zonation was pronounced, with the Capitan Reef complex in the Delaware Basin exemplifying a biodiverse buildup where sponges, calcareous algae, and bryozoans served as primary framework constructors, supporting associated faunas in a barrier reef system up to 700 meters thick.^[97]^[98] In contrast, the deep waters of Panthalassa hosted siliceous microfossils like radiolaria, which formed vast chert deposits indicative of open-ocean productivity and siliceous oozes accumulating below the photic zone.^[99]^[44] These zones occasionally experienced localized anoxia, influencing benthic distributions as noted in paleoceanographic records.^[100] A notable decline in marine diversity occurred during the Guadalupian epoch, particularly affecting tropical assemblages, where warming seas and associated environmental stress led to reduced reef-building capacities and losses among fusulinids and other invertebrates, setting the stage for further perturbations.^[101]^[102]^[103]

Terrestrial invertebrates

During the Permian Period, terrestrial invertebrates, primarily arthropods, underwent significant diversification and adaptation to increasingly varied continental environments, including forests, floodplains, and emerging arid zones. Arthropods such as insects, arachnids, myriapods, and crustaceans formed key components of these ecosystems, contributing to nutrient cycling and serving as prey for early tetrapods. Their fossil record reveals a radiation tied to the expansion of glossopterid-dominated forests in the early to middle Permian, followed by challenges from global aridification toward the period's end.^[104] Insects represented one of the most prominent groups, with early lineages like eoblattodeans—primitive cockroach-like forms (Blattodea)—appearing in the fossil record by the Early Permian, characterized by robust bodies adapted for scavenging in humid litter layers. Odonatopterans, stem-group relatives of modern dragonflies and mayflies, also proliferated, exemplified by the griffenfly Meganeuropsis permiana from the Early Permian Wellington Formation in Kansas, which achieved wingspans up to 71 cm, facilitated by elevated atmospheric oxygen levels promoting gigantism. These large insects likely faced predation pressures from synapsids such as pelycosaurs, including Dimetrodon, which occupied top carnivore niches and exerted selective forces on aerial and terrestrial arthropod populations. Plant-insect interactions, including herbivory on seed ferns and conifers, underscored co-evolutionary dynamics in these forests.^[105]^[106]^[107] Arachnids, including scorpions and spiders, expanded into drier habitats during the Permian, reflecting adaptations to the period's shifting climates. Scorpions, such as the genus Opsieobuthus, burrowed in alluvial soils beneath hygrophilous vegetation, with complete specimens from the Early Permian Leukersdorf Formation in Chemnitz, Germany, indicating a body length of about 12 cm and a transition from Carboniferous ancestors to more derived forms persisting into the Triassic. Spiders, with crown-group origins in the late Paleozoic, diversified alongside these changes, utilizing silk for prey capture in semi-arid settings. This arachnid radiation, peaking in the Permian, aligned with broader terrestrialization trends.^[108]^[109] Myriapods, particularly millipedes, thrived in moist microhabitats like leaf litter accumulations under glossopterid forests, where they decomposed organic matter and facilitated soil formation. Fossil traces and body fossils from Permian paleosols, such as those in the upper Gondwana sequence of India, suggest these detritivores fed on decaying plant debris, contributing to nutrient recycling in floodplain ecosystems. Crustaceans, though predominantly aquatic, included semi-terrestrial and freshwater forms like isopods that colonized Permian lakes and rivers. Molecular phylogenies indicate that freshwater isopod lineages, such as those in Asellota, diverged around 281 million years ago, inhabiting lentic environments amid the period's wetland expansions. These isopods, preserved in lacustrine deposits, adapted to low-oxygen freshwater settings, bridging marine origins with later terrestrial invasions.^[110] Overall diversity of terrestrial invertebrates radiated during the Guadalupian (Middle Permian) in humid forest biomes, with high species richness in orders like Blattodea and Orthoptera recorded in Euramerican and Gondwanan assemblages, driven by abundant vegetation and stable climates. However, Lopingian (Late Permian) aridity led to a decline, as evidenced by reduced insect interactions on xerophytic floras in sites like the South Urals and Karoo Basin, where generalized herbivory persisted but endophytic forms waned amid oxygen fluctuations and habitat fragmentation.^[104]^[111] Exceptional fossil sites, such as the Early Permian Elmo locality in Kansas and the Middle Permian Abrahamskraal Formation in South Africa's Karoo Basin, yield Mazon Creek-like assemblages with siderite concretions preserving soft tissues, wings, and exoskeletons of insects like grylloblattodeans and protozygopterans. Similarly, the Chemnitz petrified forest in Germany captures scorpions and millipedes in volcanic ash, offering insights into in situ behaviors and community structures. These Lagerstätten highlight the fragility of Permian invertebrate faunas leading into the end-Permian extinction.^[111]^[108]

Terrestrial vertebrates

During the Permian Period, terrestrial vertebrates diversified significantly, comprising amphibians, early amniotes, and synapsids that adapted to a range of continental environments from humid lowlands to arid interiors.^[112] Synapsids emerged as the dominant group, evolving from basal forms to more advanced lineages, while amphibians and reptiles occupied niche roles influenced by climatic shifts toward aridity.^[113] This faunal assemblage supported complex food webs, with predators preying on smaller herbivores and insects.^[114] Amphibians, primarily temnospondyls, inhabited wetland margins and semi-terrestrial settings early in the period but declined as climates dried.^[115] Eryops, a robust temnospondyl reaching lengths of about 2 meters, exemplified these predators with its powerful limbs suited for both aquatic and terrestrial locomotion in floodplain environments.^[116] By the late Permian, temnospondyl diversity waned, reflecting reduced moisture availability that favored more drought-tolerant amniotes.^[115] Early amniotes, including captorhinids and parareptiles such as pareiasaurs, thrived in semi-arid to arid zones of equatorial Pangea.^[117] Captorhinids, small herbivorous reptiles like Captorhinus, burrowed in dry soils and dispersed widely across tropical regions, correlating strongly with semi-arid conditions.^[114] Parareptiles adapted similarly, with pareiasaurs featuring armored bodies for protection in open, xeric landscapes.^[117] Synapsids dominated Permian land faunas, with pelycosaurs prevalent in the Cisuralian (early Permian) and therapsids rising in the Guadalupian and Lopingian (middle to late Permian).^[118] Pelycosaurs, comprising at least 70% of early Permian vertebrate assemblages, included carnivores like Dimetrodon, whose dorsal sail likely aided thermoregulation by absorbing solar heat.^[118]^[119] Therapsids, more mammal-like in skull structure and posture, diversified into herbivores and carnivores; dicynodonts such as Lystrosaurus became abundant in the late Permian, grazing on glossopterid floras with beak-like mouths.^[120]^[121] Major faunal provinces shaped vertebrate distributions, with the Karoo Basin in Gondwana yielding rich therapsid assemblages from floodplain deposits.^[122] In North America, red bed formations like those in Texas preserved diverse early Permian faunas, including pelycosaurs and temnospondyls in riverine settings.^[118] These provinces reflected latitudinal gradients, with higher-latitude Gondwanan sites hosting cold-adapted forms by mid-Permian.^[112] Evolutionary milestones included the rise of endothermy among therapsids, evidenced by bone histology indicating elevated metabolic rates in Permian groups like dinocephalians and dicynodonts.^[123] Herbivory expanded independently in multiple lineages, enabling exploitation of emerging seed-fern vegetation and reducing reliance on insect prey.^[124] These adaptations positioned therapsids for post-extinction dominance into the Triassic.^[120]

Permian–Triassic extinction event

Description and timing

The Permian–Triassic extinction event, also known as the end-Permian mass extinction, represents the most severe biotic crisis in Earth's history, occurring at the boundary between the Lopingian Epoch of the Permian Period and the Induan Stage of the Early Triassic, approximately 251.9 million years ago (Ma).^[125] This event unfolded over a geologically brief duration of less than 60,000 years, as determined by high-resolution cyclostratigraphic analysis of sedimentary cycles in South China sections, which reveal rapid environmental perturbations synchronous with the main pulse of extinction.^[126] In terms of scale, it eliminated approximately 81–96% of marine species and around 70% of terrestrial vertebrate species, profoundly reshaping global ecosystems and leaving selective survivors such as the dicynodont Lystrosaurus, which briefly dominated post-extinction terrestrial landscapes in the Early Triassic.^[127]^[128]^[129] Geological signatures of the event include a pronounced global negative excursion in carbon isotopes (δ¹³C), with drops of 6–8‰ in both organic and inorganic carbon records from marine sections, indicating massive disruptions to the global carbon cycle near the boundary.^[126] Additionally, a characteristic "fern spike" appears in terrestrial sedimentary records immediately above the boundary, reflecting a temporary dominance of fern-like disaster taxa in the aftermath of vascular plant community collapse.^[130] Stratigraphically, the event is precisely defined at the Global Stratotype Section and Point (GSSP) in the Meishan section of Zhejiang Province, China, where the base of the Triassic is marked by the first appearance of the conodont Hindeodus parvus in Bed 27c.^[131] The extinction unfolded in at least two distinct phases: a minor pulse at the end-Capitanian (Guadalupian-Lopingian boundary, approximately 260 Ma), which affected certain marine and terrestrial groups, and a more severe main pulse at the end-Changhsingian (latest Permian), responsible for the bulk of species losses.^[132]

Causes and consequences

The primary hypothesized trigger for the Permian–Triassic extinction event was the eruption of the Siberian Traps large igneous province, which involved the extrusion of approximately 4 million km³ of flood basalts over a geologically brief interval of less than 1 million years.^[133] This massive volcanism released an estimated 10,000–30,000 gigatons of carbon dioxide (CO₂) into the atmosphere, driving profound global warming of 8–10°C.^[134] The rapid injection of greenhouse gases disrupted the carbon cycle, amplifying climatic instability and setting off cascading environmental perturbations. Secondary factors exacerbated the crisis, including the destabilization of methane hydrates in ocean sediments, which released additional potent greenhouse gases and further intensified warming.^[135] Concurrently, elevated atmospheric CO₂ levels led to ocean acidification, with surface seawater pH dropping from around 8.0 to approximately 7.5, severely impacting calcifying marine organisms. Widespread marine anoxia, fueled by thermal stratification and reduced ocean circulation, expanded oxygen minimum zones and contributed to the loss of over 90% of marine species by suffocating aerobic life forms.^[136] The extinction's consequences included the wholesale collapse of marine and terrestrial food chains, as primary producers and basal trophic levels were decimated by acidification, anoxia, and hyperthermia, propagating starvation up through higher levels.^[137] In the Tethys Ocean, expansive "dead zones" devoid of macroscopic life persisted, marked by black shales indicative of prolonged euxinic conditions.^[138] Ecosystem recovery was markedly delayed, with marine biodiversity remaining suppressed until the Middle Triassic, approximately 5–10 million years after the event, due to lingering anoxia, elevated temperatures, and nutrient imbalances.^[139] Ongoing debates center on the relative roles of volcanism versus other mechanisms, such as an asteroid impact, though evidence for the latter remains minimal, with no confirmed crater or iridium anomaly comparable to other extinction events.^[140] On land, hypercapnia—acute CO₂ poisoning leading to respiratory acidosis—has been proposed as a key driver of terrestrial vertebrate and plant die-offs, particularly in humid environments where CO₂ accumulation in soils and burrows proved lethal.^[141] Supporting isotopic evidence includes mercury enrichment anomalies across global sections, attributed to volatilization and atmospheric transport from Siberian Traps eruptions, as well as negative excursions in sulfur isotopes signaling sulfate reduction and ocean acidification.^[142]^[143]

Economic importance

Hydrocarbon deposits

The Permian period's sedimentary basins preserved substantial hydrocarbon resources, including oil, natural gas, and coal, due to organic-rich source rocks and effective trapping mechanisms developed in marine and terrestrial environments.^[144] The Permian Basin in western Texas and southeastern New Mexico stands as the world's largest oilfield, with production dominated by unconventional resources in the Wolfcamp Shale of Cisuralian age. This formation is estimated to contain 20 billion barrels of technically recoverable oil, unlocked primarily through hydraulic fracturing and horizontal drilling techniques.^[145] As of 2025, the basin yields over 6 million barrels of oil per day, accounting for nearly half of U.S. production and playing a pivotal role in global energy markets.^[146] In the North Sea, Late Permian Zechstein evaporites act as impermeable seals overlying Rotliegendes sandstones, which form major gas reservoirs charged by underlying Carboniferous source rocks. These structures have enabled the development of some of Europe's largest natural gas fields, with the evaporite layer preventing vertical migration of hydrocarbons.^[147] Permian coal deposits, particularly from Cisuralian Gondwanan settings, represent significant resources in southern hemisphere basins. The Bowen Basin in eastern Australia hosts extensive Permian coal measures, with identified resources exceeding 20 billion tonnes, supporting major coking and thermal coal exports.^[148] In Russia, the Kuznetsk Basin contains vast Permian coal reserves estimated at 63.7 billion tonnes, making it one of the world's premier coal-producing regions.^[149] Key source rocks for Permian hydrocarbons include marine shales enriched in organic matter, deposited during episodes of oceanic anoxia that limited oxygen and preserved algal and planktonic remains. These shales, such as those in the Capitanian-Changhsingian intra-platform basins, exhibit high total organic carbon content and generate oil and gas upon maturation.^[150]

Mineral resources

The Permian period is renowned for its extensive evaporite deposits, particularly potash salts, which formed in restricted marine basins under arid conditions. In the United States, the Ochoan Salado Formation in the Carlsbad district of New Mexico hosts significant stratabound potash-bearing evaporites, including sylvite and langbeinite, discovered in 1925 and actively mined since the 1930s. These deposits have supplied a substantial portion of domestic potassium needs, with historical production exceeding millions of metric tons of potash ore. In Russia, the Lower Permian Verkhnekamskoye (Upper Kama) deposit near Solikamsk in the Perm region contains vast resources of potassium-bearing salts, estimated at over 3.8 billion metric tons, and ranks among the world's largest, contributing significantly to global supply through underground mining operations. Together, Permian evaporites from these and other basins, such as the Zechstein in Europe, account for a major share of worldwide potash production, supporting approximately 25% of global potassium fertilizer needs. Metallic minerals associated with Permian red beds and related strata also hold economic value. In Germany, the Mansfeld Basin within the Southern Permian Basin features copper mineralization in the Kupferschiefer, a Late Permian black shale overlying Rotliegendes red beds, where sediment-hosted stratabound deposits have been exploited since the 12th century. Historical mining in the Mansfeld-Sangerhausen district yielded over 2.6 million metric tons of copper from approximately 109 million metric tons of ore between 1200 and 1990, with remaining resources estimated at 860,000 metric tons of copper in 35.4 million metric tons of ore. In South Africa, uranium occurs in the Upper Permian Beaufort Group of the Karoo Basin, primarily as peneconcordant tabular deposits in fluviatile sandstones, formed through early diagenetic processes involving leaching from volcanic detritus and precipitation as coffinite and uraninite. These low-grade but extensive deposits, confined to permeable channel sandstones, represent a key resource for nuclear fuel, though exploitation has been limited by economic and environmental factors. Gypsum and halite from Permian evaporites are widely utilized in industrial applications. The Zechstein evaporite sequence in northern Europe, spanning Germany, Poland, and the United Kingdom, contains thick beds of gypsum (anhydrite) and halite, formed in a vast Late Permian basin. These minerals are extracted for construction materials, such as plasterboard from gypsum, and chemical production, including chlorine and soda ash from halite brines, with ongoing solution mining operations supporting regional industries. The economic formations extend to phosphorites in the Guadalupian Phosphoria Formation of the western United States, particularly the Meade Peak Member in Idaho, Wyoming, and Utah, which hosts beds of carbonate-fluorapatite up to 32% P₂O₅. These deposits, covering over 135,000 square miles and mined since the early 20th century, serve as a primary source of phosphate rock for fertilizers, with minor associated uranium and vanadium enhancing their value. Mining of Permian evaporites in Europe traces back to the 19th century, when deep shafts at Stassfurt in the Zechstein sequence revealed extensive salt and potash strata, leading to commercial extraction starting in 1861. This development, spurred by industrial demand for chemicals and fertilizers, involved over 20 shafts and advanced techniques like steam-powered pumps, marking a pivotal era in the region's geological resource utilization.

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Permian chronostratigraphy in Kansas | Geology - GeoScienceWorld
Jun 2, 2017 · Series of the North American standard section are, in ascending order, Wolfcampian, Leonardian, Guadalupian, and Ochoan.
[48]
Refining the chronostratigraphy of the Karoo Basin, South Africa ...
We present a composite ∼1500 m section through a large part of the Ecca Group from the Tanqua depocentre, located in the southwestern segment of the Karoo ...3 Sampling And Methodology · 4.1 Palaeomagnetism · 4.1. 1 Ecca Group...
[49]
The Permian Warchha Sandstone, Salt Range, Pakistan
The 30 to 155 m thick Early Permian (Artinskian) Warchha Sandstone of the Salt Range, Pakistan is a conglomerate, sandstone and claystone successionMissing: Visean | Show results with:Visean
[50]
(PDF) Permian ammonoid biostratigraphy - ResearchGate
Aug 5, 2025 · This monograph analyzes all available data on the biostratigraphic and biogeographical distribution of Permian ammonoids and the ecological ...
[51]
https://www.sciencedirect.com/science/article/abs/pii/S0037073809001961
[52]
https://www.researchgate.net/publication/311527517_Permian_ammonoid_biostratigraphy
[53]
https://doi.org/10.1017/CBO9781139025971
[54]
[PDF] Sensitivity of Late Permian climate to bathymetric features and ...
Evidence from stratigraphic sections of the Panthalassa, Paleo-Tethys and Neo-Tethys suggests that the oceans experienced widespread anoxia during the Late ...
[55]
The Evolution of the Tethys Region throughout the Phanerozoic: A ...
Jan 1, 2014 · The Tethyan region is a major petroleum province. The paleogeographic position and tectonic history is a major control on sedimentation ...
[56]
Permian arc evolution associated with Panthalassa subduction ...
During the Middle Permian, the ACs were accreted along the eastern margin of the South China block. The Middle Permian arc was an immature oceanic island arc ...Missing: Circum- | Show results with:Circum-
[57]
Rapid rise in atmospheric CO2 marked the end of the Late ... - Nature
Jan 6, 2025 · Weathering is thought to have decreased in intensity by the Early–Middle Permian ... reduction in seafloor spreading driving long-term decline in ...
[58]
Simulated warm polar currents during the middle Permian - Winguth
Oct 17, 2002 · During Permian stage 6 (Wordian, Kazanian) the Pangaean supercontinent was surrounded by a superocean: Panthalassa. An ocean general ...
[59]
The age and depositional environments of the lower Karoo Moatize ...
The accumulation of extensive coal deposits is one of the main features of the lower Karoo sedimentary sequences deposited in the Gondwanan basins of south- ...
[60]
The Early Permian fossil record of Gondwana and its relationship to ...
Aug 5, 2025 · Deglaciation sequences of Early Permian age in Gondwana have until now been distinguished mainly on lithological criteria by reference to ...
[61]
Global climatic and ecological correlations during the Early Permian ...
Permian brachiopods show an Asselian δ 18 O maximum in Uralian specimens, and a Sakmarian-Artinskian δ 18 O decline in Uralian and Australian specimens ...
[62]
(PDF) Simulations of Permian Climate and Comparisons with ...
Aug 6, 2025 · We use a climate model to simulate two intervals of Permian climate: the Sakmarian (ca. 280 Ma), at the end of the major Permo-Carboniferous ...
[63]
(PDF) Climate, pCO2 and terrestrial carbon cycle linkages during ...
Oct 24, 2016 · Here we present a high-resolution record of atmospheric pCO2 for 16 million years of the late Palaeozoic, developed using soil carbonate-based and fossil leaf- ...
[64]
[PDF] 6.11 Atmospheric CO2 and O2 During the Phanerozoic
During the Carboniferous and Permian, when geochemical models predict O2 levels ... Royer DL (2003) Estimating latest Cretaceous and Tertiary atmospheric CO2.
[65]
https://www.researchgate.net/publication/247530601_Simulations_of_Permian_Climate_and_Comparisons_with_Climate-Sensitive_Sediments
[66]
[PDF] Classic Upper Paleozoic reefs and bioherms of West Texas and ...
very arid climate, as evidenced by the extensive back-reef evaporite deposits. During Guadalupian and earlier time, water circulation in the Delaware Basin ...
[67]
Biological and physical evidence for extreme seasonality in central ...
Biological and physical evidence supports extreme climate in central Permian Pangea ... The change from seasonally wet Cisuralian climate to desert-like Lopingian ...Introduction · Geological Setting · Citations For The Appendix...
[68]
Climate of the Supercontinent Pangea | The Journal of Geology
By the Permian, the equatorial region of Pangea was dry, and indicators of aridity and rainfall seasonality became more widespread.
[69]
Simulations of Permian Climate and Comparisons with Climate ...
Precipitation increases with increasing CO2 levels associated with the overall increase in the intensity of the hydrologic cycle (both evaporation and ...
[70]
Latest Permian–Early Triassic paleoclimatic reconstruction by ...
Jan 1, 2022 · Here we present a paleosols study of the Permian–Triassic Shichuanhe section in the Shaanxi Province of the central North China Basin.
[71]
Carbon cycle perturbations and environmental change of the middle ...
Apr 28, 2024 · The Guadalupian (ca. ~ 259.8 Ma) mass extinction event is associated with a significant negative CIE of > − 5 ‰ disrupting the otherwise ...
[72]
High-resolution δ 13 C carb chemostratigraphy from latest ...
Large δ13C negative excursions in latest Guadalupian and Lopingian are observed. •. The end-Permian excursion represents a major reorganization of global carbon ...
[73]
[PDF] A review of climate indicators - SMU
Early Permian climate models predict a strong southern monsoon, but weaker northern monsoon ... ⁎Monsoon slightly strengthened, and seasonal precipitation.
[74]
Impacts of basin restriction on geochemistry and extinction patterns
Jan 15, 2020 · Basinal dolomites and evaporites mark periods of elevated salinity tied to sea-level lowstands, which correspond with turnovers in fusulinid and ...
[75]
Permian marine paleoecology and its implications for large-scale ...
The pronounced ecological shift was instead concurrent with the onset of deep-marine anoxic or euxinic conditions around the Guadalupian-Lopingian boundary, ...
[76]
Toward a Cenozoic history of atmospheric CO 2 - Science
Dec 8, 2023 · The new record suggests that early Cenozoic “hothouse” CO2 concentrations peaked around 1600 ppm at ~51 Ma. Near 33.9 Ma, the onset of continent ...
[77]
Wetland-Dryland Vegetational Dynamics in the Pennsylvanian Ice ...
The dominant plant groups in wetlands comprise four distinct evolutionary lineages: lycopsids, ferns and sphenopsids, all free-sporing heterosporous or ...
[78]
South African Lagerstätte reveals middle Permian Gondwanan ...
Oct 30, 2022 · The iconic plant Glossopteris, an arborescent gymnosperm, dominated these floras in the lowlands of Gondwana for over 50 million years, from ...
[79]
Floral Assemblages and Patterns of Insect Herbivory during the ...
Nov 9, 2016 · Studies of early (Cisuralian), middle (Guadalupian) and late (Lopingian) Permian age have involved field sites from a variety of tectonic and ...
[80]
Walchian conifers from the Mid-Late Pennsylvanian Conemaugh ...
Late Pennsylvanian, upland (or dryland) conifer communities were comprised of Walchia, Cordaites, and Sigillaria which produced a forest with seed ferns as an ...
[81]
[PDF] RESPONSE OF LATE CARBONIFEROUS AND EARLY PERMIAN ...
With the onset of glaciation in the Permian (López-Gamundı 1997), the flora changed dramatically with the appearance of Glossopteris and the disappearance of ...
[82]
[PDF] Callipterids of the Dunkard Group of the Appalachian basin
Were the Appalachian region to be exposed under a semi-arid to arid climate, such as that of the Permian of Texas or New Mexico, the controversy over this ...
[83]
Rapid rise in atmospheric CO2 marked the end of the Late ...
Jan 6, 2025 · The elevated CO2 established a period of transient Early Permian warmth, which profoundly transformed the environment, ecology and evolution of ...Missing: sequestration | Show results with:sequestration
[84]
Differences between subfamilies in diversification process of the ...
Among them, the Schwagerininae has 507 species, making up 74.6% of the total, and Pseudoschwagerininae has 97 species, constituting another 14.3%. This may ...
[85]
[PDF] STRATIGRAPHIC DISTRIBUTION OF BRACHIOPODS - Journals@KU
Despite this decline in absolute numbers, the Productida remained the dominant order of brachiopods throughout the Permian. In the Changhsingian Stage, for ...
[86]
Global Permian brachiopod biostratigraphy: an overview
Jan 1, 2018 · Four highly diverse brachiopod orders (Orthida, Orthotetida, Productida ... They are dominated by the brachiopods Choristites ...
[87]
Upper Permian coral reef and colonial rugose corals in northwest ...
The roles of Permian colonial corals in forming organic reefs have not been adequately assessed, although they are common fossils in the Permian strata.
[88]
Permian rugose corals of the world - Lyell Collection
Jun 8, 2017 · Two coral realms were recognized, the Tethyan Realm and the Cordilleran–Arctic–Uralian Realm. These are characterized by the families ...
[89]
Late Permian nautiloids from Baghuk Mountain (Central Iran)
Sep 24, 2025 · On four new Carboniferous nautiloids and a goniatite new to Great Britain. ... Tethyan Permian-Triassic boundary section. Fossil Record 24: 171– ...
[90]
2.3 Ammonoidea - Digital Atlas of Ancient Life
Examples are shown below of ammonoids with goniatite, ceratite, and ammonite suture patterns. Make sure that you can tell them apart. Goniatite suture patterns.
[91]
Early Asselian (Earliest Permian) Ammonoids from the Taishaku ...
Oct 5, 2020 · An early Asselian ammonoid fauna comprising nine species belonging to nine genera (Agathiceras, Neoglaphyrites, Somoholites, Shumardites, Vidrioceras, Almites, ...<|separator|>
[92]
(PDF) A new specimen of Helicoprion Karpinsky, 1899 from ...
Aug 6, 2025 · A new reconstruction of the interaction of the lower tooth whorl with the upper jaw dentition is suggested and its function is discussed. It is ...
[93]
[PDF] Fossil Localities of the Rattlesnake Creek, Western and Eastern ...
Sample I-18-70B (USGS f24175) "contains the smaller foram Climacammina sp. and the fusulinids Pseudofusulinella sp. and Schwagerina sp. It is of Early Permian ...
[94]
Geologic Formations - Guadalupe Mountains National Park (U.S. ...
Geologic History. The Permian period of geologic time occurred from 251 to 299 million years ago. The earth had already seen life diversify from simple, ...
[95]
Origin of the upper Capitan-Massive limestone (Permian ...
Jun 1, 2017 · The long-running controversy over the origin of the Capitan Formation massive limestone member concerns differing interpretations of the ...
[96]
An 80 million year oceanic redox history from Permian to Jurassic ...
Redox and radiolarian history of Panthalassa from middle Permian to Early Jurassic. The Mino-Tamba deep-water sections reveal the redox history of Panthalassa ...
[97]
Patterns and paleoenvironmental implications of end-Permian ...
Late Permian rugose corals are undoubtedly the last phylogenetic representatives of the Rugosa. These corals are widely, though sporadically, distributed ...
[98]
Middle-Late Permian mass extinction on land | GSA Bulletin
Oct 3, 2017 · Both end-Guadalupian and end-Permian were followed by short-term climatic warming, indicated by transient increases in diversity and abundance ...Introduction · International... · Antarctic Sedimentology
[99]
End-Guadalupian extinction of larger fusulinids in central Iran and ...
Jul 15, 2020 · While the late Guadalupian (late Capitanian) crisis is marked by significant declines in metazoan reef abundance and fusulinid diversity ( ...Introduction · Geologic Setting · Lithostratigraphy Of The...<|control11|><|separator|>
[100]
The end-Guadalupian (259.8 Ma) biodiversity crisis: the sixth major ...
Sep 5, 2019 · ... decline in plant diversity, along with global warming, started at the early Permian in the tropics and spread to higher latitudes at mid-Permian ...
[101]
https://pubs.geoscienceworld.org/gsa/gsabulletin/article/118/11-12/1398/519076/Middle-Late-Permian-mass-extinction-on-land
[102]
https://www.sciencedirect.com/science/article/abs/pii/S0031018220301887
[103]
Insects - GeoKansas - The University of Kansas
By the end of Permian Period, however, Meganeuropsis and many other Permian insects, became extinct in the world's largest mass extinction, a catastrophe ...
[104]
Introduction to the Pelycosaurs
Dimetrodon is the most familiar example of a pelycosaur. A powerful carnivore, Dimetrodon was the top predator of the Permian period. With its large head and ...
[105]
https://doi.org/10.1016/j.cub.2015.07.059
[106]
https://geokansas.ku.edu/insects
[107]
https://ucmp.berkeley.edu/synapsids/pelycosaurs.html
[108]
https://doi.org/10.1186/s12862-016-0634-z
[109]
New Permian fauna from tropical Gondwana | Nature Communications
Nov 5, 2015 · Here we report on a new early Permian continental tetrapod fauna from South America in tropical Western Gondwana that sheds new light on patterns of tetrapod ...
[110]
Recovery from the most profound mass extinction of all time - NIH
After the end-Guadalupian event, faunas began rebuilding complex trophic structures and refilling guilds, but were hit again by the end-Permian event. Taxonomic ...
[111]
Late Permian (Lopingian) terrestrial ecosystems - ScienceDirect.com
In the Ordos Basin, mostly located within Shaanxi Province of northeastern China, Lopingian deposits mainly consist of red fluvial deltaic and shallow ...Missing: Epoch | Show results with:Epoch
[112]
The ecology and geography of temnospondyl recovery after the ...
Mar 5, 2025 · Many Permian temnospondyls were terrestrial predators, not limited to aquatic habitats. Large water bodies are generally cooler than the ...
[113]
The discrepancy between morphological and microanatomical ...
The Eryops bones show higher variability and represent the histotypes I, III, IV and V (Table 1). For humeri and femora, the histotype seems to be directly ...
[114]
Permo-Triassic tetrapods and their climate implications - ScienceDirect
Captorhinids and pareiasaurs preferred dry climates, whereas dicynodonts preferred wetter conditions. Based on current evidence, central Pangea transitioned ...
[115]
6 The Carboniferous-Early Permian: High Oxygen, Fires, and Giants
By the beginning of the Permian Period, some 300 million years ago, the pelycosaurs made up at least 70 percent of the land vertebrate fauna. And they ...
[116]
Early Permian | Ohio Department of Natural Resources
Dec 12, 2024 · Life during the early Permian of Ohio The sails may have assisted these animals with regulation of their body temperatures through radiative ...
[117]
Niche partitioning shaped herbivore macroevolution through ... - NIH
May 14, 2021 · Here we use functional morphology and ecology to explore herbivore morphospace through the Triassic and Early Jurassic.
[118]
Breeding Young as a Survival Strategy during Earth's Greatest Mass ...
Apr 5, 2016 · Lystrosaurus may have had unusual developmental plasticity compared to Permian dicynodonts and may have been able to breed while still growing ...
[119]
[PDF] THE PERMO–TRIASSIC BOUNDARY IN THE KAROO BASIN
The Beaufort Group, the thickest and most extensive of the lithostratigraphic units of the Karoo Supergroup, is particularly rich in fossils. This attribute has ...
[120]
Whole‐body endothermy: ancient, homologous and widespread ...
In Synapsida, it has been accepted that endothermy arose within Permian therapsids. We found convincing evidence for it in Permian dinocephalians and ...
[121]
A new Carboniferous edaphosaurid and the origin of herbivory in ...
Apr 5, 2023 · Herbivory evolved independently in several tetrapod lineages during the Late Carboniferous and became more widespread throughout the Permian ...Missing: zones | Show results with:zones
[122]
Evidence from South Africa for a protracted end-Permian extinction ...
Apr 19, 2021 · The end-Permian mass extinction (ca. 251.9 Ma) was Earth's largest biotic crisis as measured by taxon last occurrences (13–15).
[123]
High-precision timeline for Earth's most severe extinction - PNAS
The extinction had a duration of 61 ± 48 ka and was preceded by the onset of a rapid reorganization of the carbon cycle, including a rapid negative spike in δ13 ...
[124]
The stability and collapse of marine ecosystems during the Permian ...
Mar 27, 2023 · As the most severe mass extinction of all time, the Permian-Triassic (P-Tr) mass extinction (PTME) was marked by losses of 81%–96% of marine ...
[125]
The tempo of mass extinction and recovery: The end-Permian example
The basic facts that must be explained are (1): (i) Extinction of 85% or more of all species in the oceans, approximately 70% of land vertebrates, and ...
[126]
The paleobiology and paleoecology of South African Lystrosaurus
Nov 24, 2020 · Lystrosaurus was one of the few tetrapods to survive the end-Permian mass extinction (EPME), the most catastrophic biotic crisis in Phanerozoic history.
[127]
Recuperation from mass extinctions - PNAS
The mass extinction at the Permian-Triassic boundary can be described as a major environmental disturbance. As such it can be seen as an extreme point in a ...
[128]
Restudy of conodont zonation and evolution across the P/T ...
The Meishan section was accepted as the GSSP for the base of the Triassic System (PTB) in 2001, with the boundary marked by the first appearance datum (FAD) of ...
[129]
When and how did the terrestrial mid-Permian mass extinction occur ...
Jul 22, 2015 · A mid-Permian (Guadalupian epoch) extinction event at approximately 260 Ma has been mooted for two decades.<|control11|><|separator|>
[130]
Magnitude and consequences of volatile release from the Siberian ...
With an estimated volume of ~ 4 × 106 km3 (Fedorenko et al., 2000), the Siberian large igneous province ranks among the largest known continental flood basalts.
[131]
Massive and rapid predominantly volcanic CO2 emission during the ...
Sep 7, 2021 · We find that a massive and rapid, predominantly volcanic CO 2 emission during the Siberian Traps volcanism is likely the trigger for the carbon isotope ...
[132]
Gas hydrate contribution to Late Permian global warming
We modeled the stability of gas hydrates through a warming Middle to Late Permian world, considering three settings for methane reservoirs: 1) terrestrial ...
[133]
Anoxia/high temperature double whammy during the Permian ...
Feb 19, 2014 · The Permian-Triassic mass extinction wiped out over 90% of marine species, leaving a depauperate ocean and protracted recovery process.
[134]
The Permian Extinction—When Life Nearly Came to an End
Oct 15, 2024 · The short-term effects alone—cold, darkness, and acid rain—would kill plants and photosynthetic plankton, the base of most food chains.
[135]
Life in the end-Permian dead zone - PNAS
In contrast to faunal records, therefore, successive pollen and spore assemblages from marine “dead zones” may provide the sample size needed to detect ...
[136]
Recovery of marine ecosystem after the Permian-Triassic mass ...
Jan 1, 2024 · The end Permian to Middle Triassic interval (∼252–242 Ma) witnessed the largest marine mass extinction and the most delayed recovery in the ...
[137]
New evidence indicates biggest extinction wasn't caused by asteroid ...
Jan 20, 2005 · They found two patterns, one showing gradual extinction over about 10 million years leading up to the boundary between the Permian and Triassic ...
[138]
killing models during the Permian–Triassic mass extinction - Journals
Sep 3, 2018 · Together, these pulses of extinction accounted for the loss of up to 96% of marine invertebrate species globally [6], and similar losses at ...<|separator|>
[139]
Mercury evidence from southern Pangea terrestrial sections for end ...
Jan 3, 2023 · Climate-forced Hg-remobilization associated with fern mutagenesis in the aftermath of the end-Triassic extinction ... Permian–Triassic mass ...
[140]
A rapid onset of ocean acidification associated with the end-Permian ...
A rapid ocean acidification event in conjunction with the end-Permian mass extinction is documented by abundant, low-δ34S marcasite in strata within and above ...Missing: spikes | Show results with:spikes
[141]
[PDF] Permian Basin - Wolfcamp Shale Play - EIA
Oct 3, 2018 · The Permian Basin of West Texas and Southeast New Mexico has generated hydrocarbons for about 100 years and supplied more than 33.4 billion ...
[142]
USGS Estimates 20 Billion Barrels of Oil in Texas' Wolfcamp Shale
Nov 15, 2016 · The Wolfcamp shale in the Midland Basin portion of Texas' Permian Basin province contains an estimated mean of 20 billion barrels of oil.
[143]
The Permian Basin in 2025
Jan 23, 2025 · Permian production is up to more than 6 million barrels per day, accounting for nearly half of all U.S. oil production. The Basin first reached ...<|separator|>
[144]
[PDF] Carboniferous-Rotliegend Total Petroleum System Description and ...
The resulting Zechstein. Group consists of thick carbonate and evaporite rocks that are largely of Late Permian age (Taylor, 1998). The Zechstein is present ...Missing: chronostratigraphy | Show results with:chronostratigraphy
[145]
Bowen Basin | Geoscience Australia
Jun 27, 2014 · The Bowen Basin also has vast coal resources, with major open cut and underground coal mines in the north of the basin. Large volumes of ...Missing: reserves Cisuralian
[146]
[PDF] A review of the AMM & CMM resources in the Kuznetsk (Kuzbass ...
The Kuzbass Coal Basin covers an area of approximately 26,000 km and is thought to contain. 2. 63.7 billion tonnes of coal reserves. The main coal-bearing ...
[147]
Organic matter enrichment model of Permian Capitanian ... - Frontiers
The Permian Capitanian-Changhsingian black shale formed in intra-platform basins are the major source rocks in Southwest China ... marine anoxic events as typical ...