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Lower Ordovician Conodonts of Europe

https://doi.org/10.1130/mem127-p21
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inferred← citeshttps://doi.org/10.5852/ejt.2021.774.1533zenodo-depositor-declared
Middle Ordovician Drepanoistodus (Vertebrata, Conodonta) from Baltica, with description of three new species
inferred← citeshttps://doi.org/10.1007/978-3-031-82911-6_28openalex-snapshot
Conodont Research: An Important Tool Applied to the Central European Variscides
inferred← citeshttps://doi.org/10.1007/978-94-009-2549-6_19openalex-snapshot
Stratigraphy and faunas of the Parautochthon and Lower Allochthon of southern Norway
inferred← citeshttps://doi.org/10.1007/978-94-017-0611-7_6openalex-snapshot
An Early Ordovician oribatid mite (Acari: Oribatida) from the island of Öland, Sweden
inferred← citeshttps://doi.org/10.1007/bf02274680openalex-snapshot
Früher Kalzitzement in skandinavischen Orthocerenkalken: Beziehungen zum Glaukonit
inferred← citeshttps://doi.org/10.1007/bf02987980openalex-snapshot
Zur Biologie, Taxonomie und Chronologie der Conodonten
inferred← citeshttps://doi.org/10.1007/bf02988161openalex-snapshot
The Hunneberg Stage (Ordovician) in the area east of St. Petersburg, north-western Russia
inferred← citeshttps://doi.org/10.1007/bf02988364openalex-snapshot
Apparatus structure of the Ordovician conodontDecoriconus peselephantis (Lindström 1955)
inferred← citeshttps://doi.org/10.1007/bf02988394openalex-snapshot
AnOistodus venustus-like conodont species from the Middle Ordovician of Baltoscandia
inferred← citeshttps://doi.org/10.1007/bf03004569openalex-snapshot
Taxonomy and distribution of the Ordovician conodontDrepanodus arcuatus Pander, 1856, and related species
inferred← citeshttps://doi.org/10.1007/bfb0010200openalex-snapshot
Global bio-events in the Ordovician?
inferred← citeshttps://doi.org/10.1007/s12549-019-00380-9openalex-snapshot
Study and Use of Upper Cambrian to Lower Ordovician conodonts in central, southern, and western Laurentia, 1933–2018
inferred← citeshttps://doi.org/10.1016/0031-0182(76)90014-6openalex-snapshot
Possible early Devonian conodontophorid provinces
inferred← citeshttps://doi.org/10.1016/0034-6667(94)00096-3openalex-snapshot
Arenigian acritarchs from Horns Udde (Öland, Sweden): a preliminary report
inferred← citeshttps://doi.org/10.1016/bs.sats.2016.10.002openalex-snapshot
Conodont and Graptolite Biostratigraphy of the Ordovician System of Argentina
inferred← citeshttps://doi.org/10.1016/j.epsl.2011.09.014openalex-snapshot
A time like our own? Radioisotopic calibration of the Ordovician greenhouse to icehouse transition
inferred← citeshttps://doi.org/10.1016/j.jop.2024.08.001openalex-snapshot
Global pattern of conodont similarity and faunal constraints during the highstand of the Evae eustatic event (late Floian, Lower Ordovician)
inferred← citeshttps://doi.org/10.1016/j.jsames.2018.03.008openalex-snapshot
Conodont biostratigraphy from the upper San Juan Formation (Middle Ordovician) at Niquivil, Argentine Precordillera
inferred← citeshttps://doi.org/10.1016/j.jsames.2020.102798openalex-snapshot
New early Ordovician conodont data from the San Juan Formation, Central Precordillera (Argentina): Biostratigraphic and paleogeographic significance
inferred← citeshttps://doi.org/10.1016/j.jsames.2021.103504openalex-snapshot
Early Ordovician conodonts from the Ullum Volcanic Center, Argentine Precordillera: Biostratigraphy, geothermometry and preservation
inferred← citeshttps://doi.org/10.1016/j.jsames.2023.104332openalex-snapshot
The Baltoniodus navis Zone in the Gualcamayo Formation (Middle Ordovician), Central Precordillera, Argentina
inferred← citeshttps://doi.org/10.1016/j.jseaes.2014.09.003openalex-snapshot
Early–Middle Ordovician conodont biofacies on the Yangtze Platform margin, South China: Applications to palaeoenvironment and sea-level changes
inferred← citeshttps://doi.org/10.1016/j.marmicro.2026.102592openalex-snapshot
Origin and evolution of the Ordovician conodont genus Kirkupodus and its significance in palaeobiogeography
inferred← citeshttps://doi.org/10.1016/j.palaeo.2006.05.002openalex-snapshot
Arenig (Middle Ordovician) ostracods from Baltoscandia: Fauna, assemblages and biofacies
inferred← citeshttps://doi.org/10.1016/j.palaeo.2011.10.020openalex-snapshot
Sulfur isotope evidence for widespread euxinia and a fluctuating oxycline in Early to Middle Ordovician greenhouse oceans
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.03.023openalex-snapshot
Conodonts from the Lower Ordovician of Morocco — Contributions to age and faunal diversity of the Fezouata Lagerstätte and peri-Gondwana biogeography
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.04.026openalex-snapshot
Upper Ordovician conodont biostratigraphy and biofacies from the Sigang section, Neixiang, Henan, central China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.03.015openalex-snapshot
The conodont Paroistodus horridus (Barnes and Poplawski) as a new biostratigraphical tool for the middle Darriwilian (Ordovician)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.04.007openalex-snapshot
Late Cambrian (Furongian) to mid-Ordovician euconodont events on Baltica: Invasions and immigrations
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.04.013openalex-snapshot
Ordovician conodonts and the Tornquist Lineament
inferred← citeshttps://doi.org/10.1016/j.palaeo.2023.111446openalex-snapshot
Coupled biostratigraphy and chemostratigraphy at Lanna, Sweden: A key section for the Floian–lower Darriwilian interval (Lower–Middle Ordovician)
inferred← citeshttps://doi.org/10.1016/j.palwor.2015.01.003openalex-snapshot
Lower–Middle Ordovician δ13C chemostratigraphy of western Baltica (Jämtland, Sweden)
inferred← citeshttps://doi.org/10.1016/j.palwor.2015.12.002openalex-snapshot
On the diachronous nature of the top of the Ordovician Kuniutan Formation on the Yangtze Platform: Implications of the conodont biostratigraphy of the Dacao section, Chongqing
inferred← citeshttps://doi.org/10.1016/j.palwor.2018.08.005openalex-snapshot
Early Ordovician sponge-bearing microbialites from Peninsular Malaysia: The initial rise of metazoans in reefs
inferred← citeshttps://doi.org/10.1016/j.palwor.2018.09.002openalex-snapshot
A new conodont biozone classification of the Ordovician System in South China
inferred← citeshttps://doi.org/10.1016/j.palwor.2020.06.006openalex-snapshot
Ordovician conodont biostratigraphy of the Willara Formation in the Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.1016/j.palwor.2022.01.005openalex-snapshot
Conodont biostratigraphy and carbon isotope chemostratigraphy of the Middle to Upper Ordovician on the western Yangtze Platform, South China
inferred← citeshttps://doi.org/10.1016/j.palwor.2023.09.003openalex-snapshot
New insights into the conodont biostratigraphy and paleobiogeography of the Katkoyeh Formation (Lower–Upper Ordovician) at the Katkoyeh Section, East-Central Iran
inferred← citeshttps://doi.org/10.1016/j.palwor.2024.04.003openalex-snapshot
New data on the Cambrian–Ordovician (Tremadocian) conodont biostratigraphy of Guizhou Province, Southwest China
inferred← citeshttps://doi.org/10.1016/j.palwor.2025.200967openalex-snapshot
New conodont fauna from the Floian (Lower Ordovician) Acoite Formation, Cordillera Oriental, Argentina
inferred← citeshttps://doi.org/10.1016/j.palwor.2025.200994openalex-snapshot
New conodont taxa and correlation of the upper San Juan Formation, Dapingian (Ordovician), at Potrerillos Creek, Argentine Precordillera
inferred← citeshttps://doi.org/10.1016/j.palwor.2026.201123openalex-snapshot
Conodont biostratigraphy and paleoecology of the Furongian–Tremadocian succession, South Kopet-Dagh Basin, Northeast Iran
inferred← citeshttps://doi.org/10.1016/j.palwor.2026.201144openalex-snapshot
Resolving the age of deformed Ordovician carbonates in the central Okcheon Belt, Korea: Conodont and brachiopod constraints and palaeogeographic implications
inferred← citeshttps://doi.org/10.1016/s0016-6995(95)80012-3openalex-snapshot
The probable origin of the ordovician conodont “Cordylodus” horridus
inferred← citeshttps://doi.org/10.1016/s0016-6995(99)80084-9openalex-snapshot
Upper Ordovician conodonts from the Bowan Park succession, central New South Wales, Australia
inferred← citeshttps://doi.org/10.1016/s0031-0182(03)00365-1openalex-snapshot
Carbon isotope record of Late Cambrian to Early Ordovician carbonates of the Argentine Precordillera
inferred← citeshttps://doi.org/10.1016/s0034-6667(01)00090-2openalex-snapshot
On the biostratigraphic significance of the Ordovician acritarch genus Liliosphaeridium on Öland, Sweden
inferred← citeshttps://doi.org/10.1016/s0920-5446(08)70347-9openalex-snapshot
Early Paleozoic Conodont Biostratigraphy in the Atlantic Borderlands
inferred← citeshttps://doi.org/10.1017/jpa.2015.43openalex-snapshot
Middle Cambrian through lowermost Ordovician conodonts from Hunan, South China
inferred← citeshttps://doi.org/10.1017/jpa.2015.54openalex-snapshot
Ordovician (middle Darriwilian-earliest Sandbian) conodonts from the Wuhai area of Inner Mongolia, North China
inferred← citeshttps://doi.org/10.1017/s0016756800003484openalex-snapshot
Conodont biozonation in the upper Arenig of Sweden
inferred← citeshttps://doi.org/10.1017/s0016756800009870openalex-snapshot
Conodonts from the lower Ordovician at Hunneberg, south-central Sweden
inferred← citeshttps://doi.org/10.1017/s0016756800018926openalex-snapshot
The middle Lanna/Volkhov Stage (middle Arenig) of Sweden and its conodont fauna
inferred← citeshttps://doi.org/10.1017/s0016756801005945openalex-snapshot
An Early to Middle Ordovician succession of conodont faunas at Mäekalda, northern Estonia
inferred← citeshttps://doi.org/10.1017/s0016756804009227openalex-snapshot
The conodont fauna in the Middle Ordovician Eoplacognathus pseudoplanus Zone of Baltoscandia
inferred← citeshttps://doi.org/10.1017/s0016756807003585openalex-snapshot
Terminal Cambrian and lowest Ordovician succession of Mexican West Gondwana: biotas and sequence stratigraphy of the Tiñu Formation
inferred← citeshttps://doi.org/10.1017/s0016756816000017openalex-snapshot
Integrated conodont biostratigraphy and carbon isotope chemostratigraphy in the Lower–Middle Ordovician of southern Sweden reveals a complete record of the MDICE
inferred← citeshttps://doi.org/10.1017/s0016756816001035openalex-snapshot
Selected Middle Ordovician key conodont species from the Santa Gertrudis Formation (Salta, Argentina): an approach to its biostratigraphical significance
inferred← citeshttps://doi.org/10.1017/s0016756819001055openalex-snapshot
New conodont records of the Los Sombreros Formation (Cambrian–Ordovician) from the Western Precordillera, Argentina: biostratigraphic and palaeoenvironmental implications
inferred← citeshttps://doi.org/10.1017/s0016756820001077openalex-snapshot
Middle Ordovician (Darriwilian) conodonts from southern Tibet, the Indian passive margin: implications for the age and correlation of the roof of the world
inferred← citeshttps://doi.org/10.1017/s0016756898001162openalex-snapshot
Occurrence of a sheeted dolerite dyke complex in the Ballantrae ophiolite, Scotland
inferred← citeshttps://doi.org/10.1017/s0022336000022940openalex-snapshot
Conodonts from the Bromide Formation (Middle Ordovician), south-central Oklahoma
inferred← citeshttps://doi.org/10.1017/s0022336000023209openalex-snapshot
Schopfodus, a new conodont genus from the upper Middle Ordovician of eastern North America
inferred← citeshttps://doi.org/10.1017/s0022336000023623openalex-snapshot
Conodonts, stratigraphy, and relative sea-level changes of the Tribes Hill Formation (Lower Ordovician, east-central New York)
inferred← citeshttps://doi.org/10.1017/s0022336000023891openalex-snapshot
Uppermost Cambrian and Lower Ordovician conodont biostratigraphy of the Survey Peak Formation (Ibexian/Tremadoc), Wilcox Pass, Alberta, Canada
inferred← citeshttps://doi.org/10.1017/s0022336000031759openalex-snapshot
SUBSPECIATION WITHIN A PUNCTUATED EQUILIBRIUM EVOLUTIONARY EVENT: PHYLOGENETIC HISTORY OF THE LOWER-MIDDLE ORDOVICIANPAROISTODUS ORIGINALIS–P. HORRIDUSCOMPLEX (CONODONTA)
inferred← citeshttps://doi.org/10.1017/s0022336000034338openalex-snapshot
Arenig (Lower Ordovician) conodonts and biozonation in the eastern Siljan district, central Sweden
inferred← citeshttps://doi.org/10.1017/s0022336000041019openalex-snapshot
Conodont biostratigraphy and paleoecology of Middle Ordovician rocks in eastern Oklahoma
inferred← citeshttps://doi.org/10.1017/s0022336000044450openalex-snapshot
Element association and morphology in some Middle Ordovician platform-equipped conodonts
inferred← citeshttps://doi.org/10.1017/s1477201907002234openalex-snapshot
The interrelationships of ‘complex’ conodonts (Vertebrata)
inferred← citeshttps://doi.org/10.1017/s1755691008007056openalex-snapshot
Morphology, evolution and stratigraphic distribution in the Middle Ordovician conodont genus Microzarkodina
inferred← citeshttps://doi.org/10.1017/s1755691024000070openalex-snapshot
Faunal dynamics and evolution of Ordovician conodonts on the Baltic side of the Tornquist Sea
inferred← citeshttps://doi.org/10.1029/2021pa004309openalex-snapshot
A Baltic Perspective on the Early to Early Late Ordovician δ 13 C and δ 18 O Records and Its Paleoenvironmental Significance
inferred← citeshttps://doi.org/10.1038/292828a0openalex-snapshot
Lower Palaeozoic strata on the Pacific Plate of North America
inferred← citeshttps://doi.org/10.1080/00167617908729103openalex-snapshot
A preliminary Ordovician biostratigraphy of Tasmania
inferred← citeshttps://doi.org/10.1080/00206818309466708openalex-snapshot
Conodont associations in Cambrian—Ordovician boundary deposits in the Malyy Karatau (South Kazakhstan)
inferred← citeshttps://doi.org/10.1080/002411601300068152openalex-snapshot
Bioerosional innovation for living in carbonate hardgrounds in the Early Ordovician of Sweden
inferred← citeshttps://doi.org/10.1080/00241160310006402openalex-snapshot
Ordovician conodont biogeography – reconsidered
inferred← citeshttps://doi.org/10.1080/00241160410004601openalex-snapshot
Billingen (Lower Arenig/Lower Ordovician) acritarchs from the East European Platform and their palaeobiogeographic significance
inferred← citeshttps://doi.org/10.1080/00288306.1975.10421557openalex-snapshot
Lower Ordovician sequence and conodonts, Mount Patriarch, North‐West Nelson, New Zealand
inferred← citeshttps://doi.org/10.1080/03115510008619526openalex-snapshot
Late Ordovician and Early Silurian conodonts from the “Uralba Beds”, northern New South Wales
inferred← citeshttps://doi.org/10.1080/03115510408619276openalex-snapshot
Middle Ordovician (Darriwilian) conodonts from allochthonous limestones in the Oakdale Formation of central New South Wales
inferred← citeshttps://doi.org/10.1080/03115510608619313openalex-snapshot
Early OrdovicianTriangulodus(Conodonta) from the Honghuayuan Formation of Guizhou, South China
inferred← citeshttps://doi.org/10.1080/03115510902844160openalex-snapshot
Early Sandbian (Late Ordovician) conodonts from the Yenwashan Formation, western Zhejiang, South China
inferred← citeshttps://doi.org/10.1080/03115510903043655openalex-snapshot
Conodont fauna and biostratigraphy of the Honghuayuan Formation (Early Ordovician) of Guizhou, South China
inferred← citeshttps://doi.org/10.1080/03115517808527788openalex-snapshot
Ordovician biostratigraphy of the Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.1080/03115518.2013.744240openalex-snapshot
Middle Ordovician (early Dapingian) conodonts in the Central Andean Basin of NW Argentina
inferred← citeshttps://doi.org/10.1080/03115518.2013.828253openalex-snapshot
Trilobites from the Middle Ordovician Stairway Sandstone, Amadeus Basin, central Australia
inferred← citeshttps://doi.org/10.1080/03115518.2013.858204openalex-snapshot
Middle Ordovician brachiopods from the Stairway Sandstone, Amadeus Basin, central Australia
inferred← citeshttps://doi.org/10.1080/03115518.2015.958295openalex-snapshot
Early Ordovician conodonts from Zhejiang Province, southeast China and their biostratigraphic and palaeobiogeographic implications
inferred← citeshttps://doi.org/10.1080/03115518.2016.1118298openalex-snapshot
Terminal Cambrian and Early Ordovician (Tremadocian) conodonts from Eastern Alborz, north-central Iran
inferred← citeshttps://doi.org/10.1080/03115518.2020.1737227openalex-snapshot
Revision of the Darriwilian (Middle Ordovician) conodonts documented by Watson (1988) from subsurface Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.1080/03115518.2020.1853235openalex-snapshot
Age correlations for the Acoite Formation (Lower Ordovician) at Aguas Blancas Creek in the Cordillera Oriental of Jujuy Province, Argentina
inferred← citeshttps://doi.org/10.1080/03115518.2020.1861325openalex-snapshot
Conodont biostratigraphy and biodiversity of the middle to Upper Ordovician near Shitai of Anhui Province, South China
inferred← citeshttps://doi.org/10.1080/03115518.2021.1914727openalex-snapshot
Trilobites from the mid-Darriwilian (Middle Ordovician) of the Amadeus Basin, central Australia
inferred← citeshttps://doi.org/10.1080/03115518.2021.2017481openalex-snapshot
Early Ordovician conodonts from Barnicarndy 1 stratigraphic well of the Southern Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.1080/03115518.2023.2172210openalex-snapshot
Revision of the Ordovician conodont speciesFahraeusodus adentatusand the new genusPohlerodus
inferred← citeshttps://doi.org/10.1080/03115518.2024.2306623openalex-snapshot
Taxonomic revision of the genus Stiptognathus (Conodonta) from the Lower Ordovician of Australia and its biostratigraphical and palaeobiogeographical significance
inferred← citeshttps://doi.org/10.1080/03115518.2026.2615101openalex-snapshot
Taxonomy, evolution and biostratigraphy of the Ordovician conodont genera Triangulodus and Tropodus
inferred← citeshttps://doi.org/10.1080/03115518008558976openalex-snapshot
Early Ordovician orthide brachiopods from southern Tasmania
inferred← citeshttps://doi.org/10.1080/03115518308619611openalex-snapshot
Ordovician nautiloids of Tasmania, Australia — Ellesmerocerida and Tarphycerida
inferred← citeshttps://doi.org/10.1080/08120098408729276openalex-snapshot
The Tremadoc series of China
inferred← citeshttps://doi.org/10.1080/11035890001224321openalex-snapshot
Early to early Middle Ordovician conodont biostratigraphy of the Gillberga quarry, northern Öland, Sweden
inferred← citeshttps://doi.org/10.1080/11035890101233129openalex-snapshot
Middle Ordovician ostracods from the Lanna and Holen Limestones, south-central Sweden
inferred← citeshttps://doi.org/10.1080/11035890501274283openalex-snapshot
Conodont biostratigraphy and sedimentary history in the upper Tremadoc at Uuga, Cape Pakri, NW Estonia
inferred← citeshttps://doi.org/10.1080/11035890701292065openalex-snapshot
Maurits Lindström – A renaissance geoscientist
inferred← citeshttps://doi.org/10.1080/11035890701292113openalex-snapshot
Ordovician limestone in Hälsingland, Sweden
inferred← citeshttps://doi.org/10.1080/11035897.2010.519440openalex-snapshot
A rare occurrence of serrate conodont elements ofPanderodusEthington in the Middle Ordovician ‘Täljsten’ interval at Kinnekulle, south Sweden
inferred← citeshttps://doi.org/10.1080/11035897.2022.2032822openalex-snapshot
First record of an Early Ordovician brachiopod and conodont fauna from Lapland, Sweden
inferred← citeshttps://doi.org/10.1080/11035899309452752openalex-snapshot
Arenig conodont successions from central Sweden
inferred← citeshttps://doi.org/10.1080/11035899409546176openalex-snapshot
The pre‐impact Ordovician Stratigraphy of the tvären bay impact structure, se Sweden
inferred← citeshttps://doi.org/10.1080/11035899609546251openalex-snapshot
Lower Ordovician conodonts, reworking, and biostratigraphy of the Orreholmen quarry, Västergötland, south‐central Sweden
inferred← citeshttps://doi.org/10.1080/11035899709546455openalex-snapshot
The lower Ordovician conodontEoplacognathus crassusChen & Zhang, 1993
inferred← citeshttps://doi.org/10.1080/11035899709546485openalex-snapshot
Conodont faunas from the upper Tremadoc at Brattefors, south‐central Sweden, and reconstruction of thePaltodusapparatus
inferred← citeshttps://doi.org/10.1080/14772019.2017.1314985openalex-snapshot
Two new early balognathid conodont genera from the Ordovician of Oman and comments on the early evolution of prioniodontid conodonts
inferred← citeshttps://doi.org/10.1111/j.1365-3121.2010.00954.xopenalex-snapshot
First Late Ordovician conodont fauna in the Betic Cordillera (South Spain): a palaeobiogeographical contribution
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2004.00431.xopenalex-snapshot
Late Ordovician vertebrates from the Bighorn Mountains of Wyoming, USA
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2008.00810.xopenalex-snapshot
EARLY ORDOVICIAN CONODONTS FROM TARUTAO ISLAND, SOUTHERN PENINSULAR THAILAND
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1970.tb00834.xopenalex-snapshot
A SUPRAGENERIC TAXONOMY OF THE CONODONTS
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1973.tb01201.xopenalex-snapshot
Didymograptus bifidus and the trans‐Atlantic correlation of the Lower Ordovician
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1975.tb01308.xopenalex-snapshot
Provinces, communities, and the proposed nektobenthic habit of Ordovician conodontophorids
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1979.tb00992.xopenalex-snapshot
The structure and evolution of Ordovician conodont apparatuses
inferred← citeshttps://doi.org/10.1111/j.1502-3931.2008.00148.xopenalex-snapshot
The base of the Middle Ordovician in China with special reference to the succession at Hengtang near Jiangshan, Zhejiang Province, southern China
inferred← citeshttps://doi.org/10.1111/let.12191openalex-snapshot
Conodonts in Ordovician biostratigraphy
inferred← citeshttps://doi.org/10.1111/pala.12089openalex-snapshot
Katian ( U pper O rdovician) conodonts from W ales
inferred← citeshttps://doi.org/10.1111/pala.12348openalex-snapshot
Baltoscandian conodont biofacies fluctuations and their link to Middle Ordovician (Darriwilian) global cooling
inferred← citeshttps://doi.org/10.1127/0077-7749/2013/0311openalex-snapshot
The Ordovician conodont Trapezognathus Lindström, 1955 in the Andean Basin, Argentina
inferred← citeshttps://doi.org/10.1127/1860-1804/2013/0003openalex-snapshot
Conodont biostratigraphy in the Early to Middle Ordovician strata of the Oslobreen Group in Ny Friesland, Svalbard
inferred← citeshttps://doi.org/10.1130/b38311.1openalex-snapshot
High-resolution integrated conodont biostratigraphy and carbon isotope (δ13Ccarb) chemostratigraphy of the Ordovician of Sweden, with comparison to South China and North America
inferred← citeshttps://doi.org/10.1134/s0031030124601117openalex-snapshot
Multielement Conodonts from the Upper Ordovician of the Siberian Platform
inferred← citeshttps://doi.org/10.1139/cjes-38-10-1387openalex-snapshot
Conodonts from the Kechika Formation and Road River Group (Lower to Upper Ordovician) of the Cassiar Terrane, northern British Columbia
inferred← citeshttps://doi.org/10.1139/e03-009openalex-snapshot
First Middle Ordovician biota from southern New Brunswick: stratigraphic and tectonic implications for the evolution of the Avalon continent
inferred← citeshttps://doi.org/10.1139/e07-047openalex-snapshot
Conodont biostratigraphy of the latest Cambrian - Early Ordovician upper McKay Group, southeastern British Columbia
inferred← citeshttps://doi.org/10.1139/e17-124openalex-snapshot
Tectonic and paleogeographic significance of Late Ordovician conodonts in the Canadian Appalachians
inferred← citeshttps://doi.org/10.1139/e76-002openalex-snapshot
Revision of the Oxford Formation (Arenig) of southeastern Ontario and northern New York State
inferred← citeshttps://doi.org/10.1139/e85-120openalex-snapshot
Simple-cone conodont taxa from the Cobbs Arm Limestone (Middle Ordovician), New World Island, Newfoundland
inferred← citeshttps://doi.org/10.1144/gsjgs.143.1.0177openalex-snapshot
Conodont palaeobiogeography and thermal maturation in the Caledonides
inferred← citeshttps://doi.org/10.1144/gsl.sp.1986.020.01.07openalex-snapshot
Biostratigraphic integration of Ordovician graptolite and conodont zones—a regional review
inferred← citeshttps://doi.org/10.1144/jgs2024-290openalex-snapshot
Hirnantian (Late Ordovician) through Aeronian (Llandovery, early Silurian) conodonts from the Whippoorwill, Brassfield and golden Brassfield formations of the North American Midwest Basins and Arches region, USA
inferred← citeshttps://doi.org/10.1144/jm.10.1.51openalex-snapshot
Conodonts of the Dounans Limestone, Highland Border Complex, Scotland
inferred← citeshttps://doi.org/10.1144/jm.19.1.45openalex-snapshot
Conodont micropalaeontology of mid-Ordovician aged limestone clasts from Lower Old Red Sandstone conglomerates, Lanark and Strathmore basins, Midland Valley, Scotland
inferred← citeshttps://doi.org/10.1144/pygs.51.1.9openalex-snapshot
Conodont biostratigraphy of the attenuated Dent Group (upper Ordovician) at Hartley Ground, Broughton in Furness, Cumbria, UK
inferred← citeshttps://doi.org/10.1144/sjg26010047openalex-snapshot
A new Lower Ordovician conodont faunule from the Northern Belt of the Southern Uplands
inferred← citeshttps://doi.org/10.1144/sjg38020069openalex-snapshot
Conodont biostratigraphy of the Crawford Group, Southern Uplands, Scotland
inferred← citeshttps://doi.org/10.1144/sp532-2022-157openalex-snapshot
The Ordovician of Scandinavia: a revised regional stage classification
inferred← citeshttps://doi.org/10.1144/sp533-2022-128openalex-snapshot
Regional synthesis of the Ordovician geology and stratigraphy of China
inferred← citeshttps://doi.org/10.1344/105.000000247openalex-snapshot
New late Tremadocian (Early Ordovician) conodont and graptolite records from the southern South American Gondwana margin (Eastern Cordillera, Argentina)
inferred← citeshttps://doi.org/10.1344/105.000000248openalex-snapshot
An Early Ordovician (Floian) Conodont Fauna from the Eastern Cordillera of Peru (Central Andean Basin)
inferred← citeshttps://doi.org/10.1344/105.000001382openalex-snapshot
Ordovician conodonts from the Mithaka Formation (Georgina Basin, Australia). Regional and paleobiogeographical implications
inferred← citeshttps://doi.org/10.1344/105.000001691openalex-snapshot
Ordovician conodonts of the Devendeus Formation at the Angosto de La Quesera (Cordillera Oriental of Salta, Argentina): Taxonomic considerations and biostratigraphic significance
inferred← citeshttps://doi.org/10.1353/ijes.2024.a935020openalex-snapshot
Late Darriwilian (Middle Ordovician) conodonts from eastern and southeastern Ireland
inferred← citeshttps://doi.org/10.1666/0022-3360(2000)074<0092:sngcil>2.0.co;2openalex-snapshot
STIPTOGNATHUSNEW GENUS (CONODONTA: IBEXIAN, LOWER ORDOVICIAN), AND THE APPARATUS OFSTIPTOGNATHUS BOREALIS(REPETSKI, 1982)
inferred← citeshttps://doi.org/10.1666/0022-3360(2000)074<1122:muocoe>2.0.co;2openalex-snapshot
MOHAWKIAN (UPPER ORDOVICIAN) CONODONTS OF EASTERN NORTH AMERICA AND BALTOSCANDIA
inferred← citeshttps://doi.org/10.1666/0022-3360(2003)077<0146:cfaptb>2.0.co;2openalex-snapshot
CONODONTS FROM A PLATFORM-TO-BASIN TRANSECT, LOWER ORDOVICIAN TO LOWER SILURIAN, NORTHEASTERN BRITISH COLUMBIA, CANADA1
inferred← citeshttps://doi.org/10.1666/0022-3360(2003)077<0721:eaamis>2.0.co;2openalex-snapshot
ELEMENT ASSOCIATION AND MORPHOLOGY IN SOME MIDDLE ORDOVICIAN PLATFORM-EQUIPPED CONODONTS
inferred← citeshttps://doi.org/10.1666/0022-3360(2003)077<0958:cfabot>2.0.co;2openalex-snapshot
CONODONT FAUNA AND BIOSTRATIGRAPHY OF THE OUTRAM, SKOKI, AND OWEN CREEK FORMATIONS (LOWER TO MIDDLE ORDOVICIAN), WILCOX PASS, ALBERTA, CANADA
inferred← citeshttps://doi.org/10.1666/0022-3360(2005)079<0433:eoetmt>2.0.co;2openalex-snapshot
EARLIEST ORDOVICIAN (EARLY TO MIDDLE TREMADOCIAN) RADIOLARIAN FAUNAS OF THE COW HEAD GROUP, WESTERN NEWFOUNDLAND
inferred← citeshttps://doi.org/10.1666/0022-3360(2007)81[19:ocftsa]2.0.co;2openalex-snapshot
ORDOVICIAN CONODONTS FROM THE SATUN AREA, SOUTHERN PENINSULAR THAILAND
inferred← citeshttps://doi.org/10.1666/04-128.1openalex-snapshot
The Oldest Bryozoans: New Evidence From the Late Tremadocian (Early Ordovician) of East Yangtze Gorges in China
inferred← citeshttps://doi.org/10.1666/05077.1openalex-snapshot
LATE ORDOVICIAN TO EARLY SILURIAN CONODONT FAUNAS FROM THE KOLYMA TERRANE, OMULEV MOUNTAINS, NORTHEAST RUSSIA, AND THEIR PALEOBIOGEOGRAPHIC AFFINITY
inferred← citeshttps://doi.org/10.1666/07-058.1openalex-snapshot
Biostratigraphy and paleobiogeography of Middle and Late Ordovician conodonts from the Langkawi Islands, northwestern peninsular Malaysia
inferred← citeshttps://doi.org/10.1666/10-076.1openalex-snapshot
Tremadocian (Lower Ordovician) sea-level changes and biotas on the Avalon microcontinent
inferred← citeshttps://doi.org/10.18261/8200067378-1983-05openalex-snapshot
Biogeography, evolutionary relationships, and biostratigraphic significance of Ordovician platform conodonts
inferred← citeshttps://doi.org/10.18261/8200095487-1984openalex-snapshot
Conodonts of the Middle Ordovician Table Head Formation, western Newfoundland
inferred← citeshttps://doi.org/10.18261/9781405169882-2001openalex-snapshot
Conodont biostratigraphy and taxonomy of the Ordovician shelf margin deposits in the Scandinavian Caledonides
inferred← citeshttps://doi.org/10.18261/9781405169882-2001-01openalex-snapshot
Conodont biostratigraphy and taxonomy of the Ordovician shelf margin deposits in the Scandinavian Caledonides
inferred← citeshttps://doi.org/10.18814/epiiugs/2005/v28i2/004openalex-snapshot
A proposed GSSP for the base of the Middle Ordovician Series: the Huanghuachang section, Yichang, China
inferred← citeshttps://doi.org/10.18814/epiiugs/2006/v29i1/001openalex-snapshot
A proposed Global Boundary Stratotype Section and Point for the base of the Middle Ordovician Series: The Niquivil section, Precordillera of San Juan, Argentina
inferred← citeshttps://doi.org/10.18814/epiiugs/2009/v32i2/003openalex-snapshot
The Global Stratotype Section and Point for the base of the Middle Ordovician Series and the Third Stage (Dapingian)
inferred← citeshttps://doi.org/10.2113/rgg20234641openalex-snapshot
Late Ordovician Shelf Deposition in Northern Gorny Altai: Lithology, Faunas, and Paleogeography
inferred← citeshttps://doi.org/10.2113/rgg20254892openalex-snapshot
ORDOVICIAN MARINE SEDIMENTS OF TYVA, ALTAI-SAYAN FOLDED AREA: BIOSTRATIGRAPHY, FACIES, COMPOSITION AND SPECIFIC FEATURES OF FAUNA ASSEMBLAGES AND PALEOGEOGRAPHIC LOCALITY
inferred← citeshttps://doi.org/10.21701/bolgeomin.124.4.002openalex-snapshot
The Baltoniodus triangularis Conodont Zone in the South American Lower-Paleozoic Central Andean Basin: the Alto del Cóndor Formation of northern Argentina
inferred← citeshttps://doi.org/10.2307/1486135openalex-snapshot
Palynomorphs, Conodonts and Associated Graptolites from the Ordovician Los Azules Formation, Central Precordillera, Argentina
inferred← citeshttps://doi.org/10.2517/1342-8144(2008)12[181:roeamo]2.0.co;2openalex-snapshot
Reinterpretation of Early and Middle Ordovician conodonts from the Thong Pha Phum area, western Thailand, in the context of new material from western and northern Thailand
inferred← citeshttps://doi.org/10.2517/1342-8144-17.2.179openalex-snapshot
A New Middle Ordovician Conodont Fauna from the Thong Pha Phum Area of Western Thailand
inferred← citeshttps://doi.org/10.2517/pr210035openalex-snapshot
Early Paleozoic Plankton Evolution in the Paleo-Asian Ocean: Insights from New and Reviewed Fossil Records from the Gorny Altai, West Siberia
inferred← citeshttps://doi.org/10.2517/prpsj.10.215openalex-snapshot
Lower and Middle Ordovician conodonts from the Thung Song and Thung Wa areas, southern peninsular Thailand
inferred← citeshttps://doi.org/10.26749/rstpp.114.201openalex-snapshot
Lithostratigraphy and biostratigraphy of the Florentine Valley Formation in the Tim Shea area, southwest Tasmania
inferred← citeshttps://doi.org/10.3140/bull.geosci.1453openalex-snapshot
Dapingian-lower Darriwilian (Ordovician) stratigraphic gap in the Faraghan Mountains, Zagros Ranges, south-eastern Iran
inferred← citeshttps://doi.org/10.3140/bull.geosci.1759openalex-snapshot
Taxonomy, biostratigraphy and biofacies of an Upper Ordovician (Katian) conodont fauna from the Casaio Formation, Northwest Spain
inferred← citeshttps://doi.org/10.3140/bull.geosci.1847openalex-snapshot
New data on conodonts and ostracods of the Katkoyeh Formation (Lower-Upper Ordovician) at the Banestan Section of East-Central Iran: biostratigraphical and palaeobiogeographical significance
inferred← citeshttps://doi.org/10.3176/earth.2011.1.01openalex-snapshot
Lower and Middle Ordovician conodonts from the subsurface of SE Estonia and adjacent Russia; pp. 1–21
inferred← citeshttps://doi.org/10.3176/earth.2012.3.01openalex-snapshot
Conodont dating of the Middle Ordovician breccia cap-rock limestone on Osmussaar Island, northwestern Estonia; pp. 133–148
inferred← citeshttps://doi.org/10.3176/geol.1983.4.02openalex-snapshot
СТРАТИГРАФИЯ АРЕНИГСКИХ И ЛЛАНВИРНСКИХ ОТЛОЖЕНИЙ (ЛАТОРПСКИЙ–ЛАСНАМЯГИСКИЙ ГОРИЗОНТЫ) ВОСТОЧНОЙ ЛИТВЫ И СЕВЕРО-ЗАПАДНОЙ БЕЛОРУССИИ
inferred← citeshttps://doi.org/10.3176/geol.1989.2.05openalex-snapshot
ON THE CORRELATION OF THE TREMADOCIAN AND ARENIGIAN BOUNDARY BEDS IN THE EAST BALTIC
inferred← citeshttps://doi.org/10.3176/geol.1989.2.06openalex-snapshot
LOWER ORDOVICIAN (ONTIKAN) CONODONT BIOSTRATIGRAPHY IN SCANDINAVIA
inferred← citeshttps://doi.org/10.3176/geol.2006.2.03openalex-snapshot
The Early Ordovician trilobite distribution and zonation of the East Baltic
inferred← citeshttps://doi.org/10.3176/geol.2006.3.02openalex-snapshot
Conodonts of the Kiviõli Member, Viivikonna Formation (Upper Ordovician) in the Kohtla section, Estonia
inferred← citeshttps://doi.org/10.37570/bgsd-1984-33-24openalex-snapshot
Lower Ordovician conodonts from Washington Land, western North Greenland
inferred← citeshttps://doi.org/10.37570/bgsd-1996-43-07openalex-snapshot
Upper Ordovician conodonts kom Bornholm and possible migration routes in the Palaeotethys Ocean
inferred← citeshttps://doi.org/10.37570/bgsd-2003-50-06openalex-snapshot
An integrated biostratigraphical analysis of the Volkhov–Kunda (Lower Ordovician) succession at Fågelsång, Scania, Sweden
inferred← citeshttps://doi.org/10.37570/bgsd-2004-51-04openalex-snapshot
Ordovician stratigraphy of the Kovel-1 well (Volkhov–Haljala) in the Volynia region, northwestern Ukraine
inferred← citeshttps://doi.org/10.37570/bgsd-2005-52-18openalex-snapshot
Barrandegnathus n. gen. (conodonta) from the Komstad Limestone (lower Mid Ordovician), Scandinavia, and its palaeogeographical significance
inferred← citeshttps://doi.org/10.3853/j.0067-1975.57.2005.1448openalex-snapshot
Revision of two prioniodontid species (Conodonta) from the Early Ordovician Honghuayuan Formation of Guizhou, South China
inferred← citeshttps://doi.org/10.3853/j.0067-1975.61.2009.1520openalex-snapshot
Biogeographic and biostratigraphic implications of the Serratognathus bilobatus fauna (Conodonta) from the Emanuel Formation (Early Ordovician) of the Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.3853/j.0067-1975.63.2011.1586openalex-snapshot
Middle to Late Ordovician (Darriwilian-Sandbian) conodonts from the Dawangou section, Kalpin area of the Tarim Basin, northwestern China
inferred← citeshttps://doi.org/10.4095/134056openalex-snapshot
Uppermost Cambrian and Lower Ordovician acritarchs and Lower Ordovician Chitinozoans from Wilcox Pass, Alberta
inferred← citeshttps://doi.org/10.4202/app.00215.2015openalex-snapshot
A Darriwilian (Middle Ordovician) bivalve-dominated molluscan fauna from the Stairway Sandstone, Amadeus Basin, central Australia
inferred← citeshttps://doi.org/10.5027/andgeov45n2-3056openalex-snapshot
Bioestratigrafía y provincialismo de conodontes del tramo medio-superior de la Formación San Juan en el cerro Viejo de Huaco, Precordillera, Argentina
inferred← citeshttps://doi.org/10.5027/andgeov46n1-3141openalex-snapshot
Early Ordovician conodonts from the Santa Rosita Formation at Pantipampa, Iruya area, northwestern Argentina
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