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Evolution and Extinction Rate Controls.

https://doi.org/10.2307/2412728
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inferred← citeshttps://doi.org/10.5281/zenodo.13271742openalex-extracted
A low diversity shallow water lingulid brachiopod-gastropod association from the Upper Ordovician of Kyrgyz Range
inferred← citeshttps://doi.org/10.1002/(sici)1099-1034(199612)31:4<359::aid-gj713>3.0.co;2-kopenalex-snapshot
Late Llandovery thelodonts and conodonts from the Kilbride Formation, Co. Galway, western Ireland
inferred← citeshttps://doi.org/10.1002/(sici)1099-1034(199911/12)34:4<321::aid-gj809>3.0.co;2-iopenalex-snapshot
Brachiopod survival and recovery from the latest Ordovician mass extinctions in South China
inferred← citeshttps://doi.org/10.1002/9781118906651.ch1openalex-snapshot
A new Silurian (Llandovery, Telychian) sponge assemblage from Gotland, Sweden
inferred← citeshttps://doi.org/10.1002/9781119412595openalex-snapshot
Ordovician rhynchonelliformean brachiopods from Co. Waterford, SE Ireland: Palaeobiogeography of the Leinster Terrane
inferred← citeshttps://doi.org/10.1002/gj.1017openalex-snapshot
Ampheristocystis, a Silurian (Lower Wenlock) eocrinoid (Echinodermata, Blastozoa) from Indiana
inferred← citeshttps://doi.org/10.1002/gj.1038openalex-snapshot
Facies development, depositional settings and sequence stratigraphy across the Ordovician–Silurian boundary: a new perspective from the Barrandian area of the Czech Republic
inferred← citeshttps://doi.org/10.1002/gj.1040openalex-snapshot
β‐diversity fluctuations in Early–Mid Ordovician brachiopod communities of South China
inferred← citeshttps://doi.org/10.1002/gj.3350160205openalex-snapshot
Faunas from the upper silurian (upper ludlovian) in the ludlow‐much wenlock district, England
inferred← citeshttps://doi.org/10.1002/gj.880openalex-snapshot
Do all mass extinctions represent an ecological crisis? Evidence from the Late Ordovician
inferred← citeshttps://doi.org/10.1002/mmng.20020050111openalex-snapshot
A Middle-Late Devonian fish fauna from the Sierra de Perijá, western Venezuela, South America
inferred← citeshttps://doi.org/10.1002/spp2.1459openalex-snapshot
Trilobites of trinucleid, raphiophorid and cyclopygid associations from the Ordovician (Darriwilian – early Katian) of the west Balkhash region and Betpak‐Dala, Central Kazakhstan
inferred← citeshttps://doi.org/10.1007/978-1-4613-8271-3_2openalex-snapshot
Evolutionary Stasis in the Elephant-Shrew, Rhynchocyon
inferred← citeshttps://doi.org/10.1007/978-1-4615-0161-9_9openalex-snapshot
Predation on Brachiopods
inferred← citeshttps://doi.org/10.1007/978-1-4615-6956-5_9openalex-snapshot
Community Evolution and Rates of Cladogenesis
inferred← citeshttps://doi.org/10.1007/978-1-4684-1410-3_7openalex-snapshot
Populations and communities
inferred← citeshttps://doi.org/10.1007/978-1-4684-1410-3_8openalex-snapshot
Palaeobiogeography
inferred← citeshttps://doi.org/10.1007/978-1-4757-0740-3_14openalex-snapshot
Diversification, Faunal Change, and Community Replacement during the Ordovician Radiations
inferred← citeshttps://doi.org/10.1007/978-1-4757-0740-3_5openalex-snapshot
Taphonomic Feedback Ecological Consequences of Shell Accumulation
inferred← citeshttps://doi.org/10.1007/978-3-030-52086-1_5openalex-snapshot
Criticism, Resistance, a Glimmer of Hope
inferred← citeshttps://doi.org/10.1007/978-3-319-15045-1_6openalex-snapshot
Networks and Hierarchies: Approaching Complexity in Evolutionary Theory
inferred← citeshttps://doi.org/10.1007/978-3-642-31721-7_2openalex-snapshot
Testing the Taxonomy and Phylogeny of Eastern North American Atrypid Brachiopods: A Geometric Morphometric Approach
inferred← citeshttps://doi.org/10.1007/978-3-642-69124-9_3openalex-snapshot
Neritic Sedimentation of the Lower and Middle Devonian in the Rheinische Schiefergebirge East of the River Rhine
inferred← citeshttps://doi.org/10.1007/978-3-642-70831-2_13openalex-snapshot
Causes and Consequences of Extinction
inferred← citeshttps://doi.org/10.1007/978-3-642-70831-2_15openalex-snapshot
Phanerozoic Overview of Mass Extinction
inferred← citeshttps://doi.org/10.1007/978-3-642-75829-4_19openalex-snapshot
Event-Stratification in Nummulite Accumulations and in Shell Beds from the Eocene of Egypt
inferred← citeshttps://doi.org/10.1007/978-3-642-79634-0_10openalex-snapshot
Silurian Bio-Events
inferred← citeshttps://doi.org/10.1007/978-3-642-79634-0_3openalex-snapshot
Evaluating Paleontologic Data Relating to Bio-Events
inferred← citeshttps://doi.org/10.1007/978-3-642-79634-0_4openalex-snapshot
Patterns of Phanerozoic Extinction: a Perspective from Global Data Bases
inferred← citeshttps://doi.org/10.1007/978-3-642-84153-8_14openalex-snapshot
Northern Appalachians: Avalon and Meguma Terranes
inferred← citeshttps://doi.org/10.1007/978-3-642-84640-3_6openalex-snapshot
Stratigraphy, Biogeography and Climatic Relationships of the Alpine Palaeozoic
inferred← citeshttps://doi.org/10.1007/978-90-481-3428-1_2openalex-snapshot
Coordinated Stasis Reconsidered: A Perspective at Fifteen Years
inferred← citeshttps://doi.org/10.1007/978-90-481-3428-1_22openalex-snapshot
The Late Middle Devonian (Givetian) Global Taghanic Biocrisis in Its Type Area (Northern Appalachian Basin): Geologically Rapid Faunal Transitions Driven by Global and Local Environmental Changes
inferred← citeshttps://doi.org/10.1007/978-90-481-8643-3_3openalex-snapshot
Taphonomic Bias in Shelly Faunas Through Time: Early Aragonitic Dissolution and Its Implications for the Fossil Record
inferred← citeshttps://doi.org/10.1007/978-90-481-8643-3_4openalex-snapshot
Comparative Taphonomy and Sedimentology of Small-Scale Mixed Carbonate/Siliciclastic Cycles: Synopsis of Phanerozoic Examples
inferred← citeshttps://doi.org/10.1007/978-94-009-0401-9_10openalex-snapshot
The Avalon composite terrane of Nova Scotia
inferred← citeshttps://doi.org/10.1007/978-94-011-5874-9_7openalex-snapshot
How do rare species avoid extinction? A paleontological view
inferred← citeshttps://doi.org/10.1007/978-94-017-0443-4_14openalex-snapshot
Macroevolutionary Events and the Origin of Higher Taxa
inferred← citeshttps://doi.org/10.1007/bf00000396openalex-snapshot
On progressive evolution and competitive extinction
inferred← citeshttps://doi.org/10.1007/bf01787459openalex-snapshot
Coral associations of the Pleistocene Ironshore Formation, Grand Cayman
inferred← citeshttps://doi.org/10.1007/bf02406725openalex-snapshot
Adaptive nature of interspecies variation of histone H1 in insects
inferred← citeshttps://doi.org/10.1007/bf02875250openalex-snapshot
Chief sources of brachiopod recovery from the end Ordovician mass extinction with special references to progenitors
inferred← citeshttps://doi.org/10.1007/bf02989436openalex-snapshot
Eine ruhigwasser-taphozönose aus einem wenlock-geschiebe (untersilur)
inferred← citeshttps://doi.org/10.1007/bf03042852openalex-snapshot
Devonian conodont biochronology in geologic time calibration
inferred← citeshttps://doi.org/10.1007/bf03042948openalex-snapshot
The frasnian-famennian conodont mass extinction and recovery in South China
inferred← citeshttps://doi.org/10.1007/bf03043222openalex-snapshot
Late Early Devonian (Late Emsian) eospiriferinid brachiopods from Shellabarger Pass, south-central Alaska, and their biogeographic importance; further evidence for a Siberian origin of the Farewell and allied Alaskan accreted terranes
inferred← citeshttps://doi.org/10.1007/bf03043736openalex-snapshot
Conodont community structure around the “Kellwasser mass extinction event” (Frasnian/Famennian boundary interval)
inferred← citeshttps://doi.org/10.1007/bf03184429openalex-snapshot
A new delthyridoid spiriferid genus from the Dra Valley, Morocco, and its phylogenetic affinities (Brachiopoda, Lower Devonian)
inferred← citeshttps://doi.org/10.1007/bfb0010189openalex-snapshot
Ecostratigraphic criteria for evaluating the magnitude, character and duration of bioevents
inferred← citeshttps://doi.org/10.1007/bfb0010190openalex-snapshot
Global bioevents and the question of periodicity
inferred← citeshttps://doi.org/10.1007/bfb0010202openalex-snapshot
Reflection of possible global Devonian events in the Barrandian area, C.S.S.R.
inferred← citeshttps://doi.org/10.1007/bfb0011131openalex-snapshot
Phanerozoic extinctions: How similar are they to each other?
inferred← citeshttps://doi.org/10.1007/bfb0011140openalex-snapshot
Silurian and pre-Upper Devonian bio-events
inferred← citeshttps://doi.org/10.1007/s00114-004-0586-9openalex-snapshot
Extinction may not be forever
inferred← citeshttps://doi.org/10.1007/s00114-021-01766-6openalex-snapshot
Teratological trilobites from the Silurian (Wenlock and Ludlow) of Australia
inferred← citeshttps://doi.org/10.1007/s00531-004-0412-9openalex-snapshot
Neoproterozoic?Early Paleozoic evolution of peri-Gondwanan terranes: implications for Laurentia-Gondwana connections
inferred← citeshttps://doi.org/10.1007/s10347-006-0083-zopenalex-snapshot
Palaeoenvironmental implications of Palaeomicrocodium in Upper Devonian microbial mounds of the Chernyshev Swell, Timan-northern Ural Region
inferred← citeshttps://doi.org/10.1007/s10347-007-0133-1openalex-snapshot
High-energy sedimentary events in lagoonal successions of the Upper Silurian of Podolia, Ukraine
inferred← citeshttps://doi.org/10.1007/s11430-010-0005-3openalex-snapshot
Expansion of the Cathaysian Oldland through the Ordovician-Silurian transition: Emerging evidence and possible dynamics
inferred← citeshttps://doi.org/10.1007/s11430-017-9165-yopenalex-snapshot
A deep water shelly fauna from the uppermost Ordovician in northwestern Hunan, South China and its paleoecological implications
inferred← citeshttps://doi.org/10.1007/s11430-017-9258-0openalex-snapshot
Silurian integrative stratigraphy and timescale of China
inferred← citeshttps://doi.org/10.1007/s12517-020-05908-4openalex-snapshot
Niche partitioning among the Mesozoic echinoderms: biotic vs abiotic traits
inferred← citeshttps://doi.org/10.1007/s12542-009-0048-yopenalex-snapshot
Leonispirifer leonensis gen. et sp. nov., a rare new delthyridoid spiriferid brachiopod from northern Spain (Brachiopoda, Lower Devonian)
inferred← citeshttps://doi.org/10.1007/s12542-010-0088-3openalex-snapshot
Strophomenidae, Leptostrophiidae, Strophodontidae and Shaleriidae (Brachiopoda, Strophomenida) from the Silurian of Gotland, Sweden
inferred← citeshttps://doi.org/10.1007/s12542-013-0213-1openalex-snapshot
The Afro–South American brachiopod Castellaroina Boucot from the Silurian of the Argentine Precordillera: its origin and phylogenetic relationships
inferred← citeshttps://doi.org/10.1007/s12549-017-0289-9openalex-snapshot
Comparative palynofacies, magnetic susceptibility and cyclicity of the Middle Devonian Müllertchen Section (Eifel area, Germany)
inferred← citeshttps://doi.org/10.1007/s13358-012-0050-yopenalex-snapshot
Taphonomy and palaeoecology of the green Devonian gypidulid brachiopods from the Aferdou El Mrakib, eastern Anti-Atlas, Morocco
inferred← citeshttps://doi.org/10.1016/0012-821x(80)90250-2openalex-snapshot
The Ordovician, Silurian and Devonian time scales
inferred← citeshttps://doi.org/10.1016/0012-821x(80)90251-4openalex-snapshot
Discussion of a paper by McKerrow, Lambert and Chamberlain on the Ordovician, Silurian and Devonian time scales
inferred← citeshttps://doi.org/10.1016/0012-8252(96)00029-3openalex-snapshot
Island-arc carbonates: characterization and recognition in the ancient geologic record
inferred← citeshttps://doi.org/10.1016/0016-6995(92)80101-iopenalex-snapshot
Brachiopodes et biostratigraphie de la Formation de Los Espejos, Siluro-Dévonien de la Précordillère (NW Argentine)
inferred← citeshttps://doi.org/10.1016/0016-7037(82)90382-9openalex-snapshot
Violent volcanism, stagnant oceans and some inferences regarding petroleum, strata-bound ores and mass extinctions
inferred← citeshttps://doi.org/10.1016/0022-5193(82)90273-9openalex-snapshot
Extinctive evolution
inferred← citeshttps://doi.org/10.1016/0031-0182(74)90012-1openalex-snapshot
Facies distribution patterns of some marine benthic faunas in early paleozoic platform environments
inferred← citeshttps://doi.org/10.1016/0031-0182(75)90004-8openalex-snapshot
Middle gaspé limestones communities on the forillon Peninsula, Quebec, Canada (Siegenian, Lower Devonian)
inferred← citeshttps://doi.org/10.1016/0031-0182(75)90024-3openalex-snapshot
Wenlock carbonate, level bottom, brachiopod-dominated communities from Wales and the Welsh Borderland
inferred← citeshttps://doi.org/10.1016/0031-0182(77)90014-1openalex-snapshot
Biogeography of late Silurian and devonian rugose corals
inferred← citeshttps://doi.org/10.1016/0031-0182(77)90021-9openalex-snapshot
Generic longevity of articulate brachiopods in relation to the mode of stabilization on the substrate
inferred← citeshttps://doi.org/10.1016/0031-0182(77)90032-3openalex-snapshot
Eustacy during the Cretaceous: Its implications and importance
inferred← citeshttps://doi.org/10.1016/0031-0182(78)90013-5openalex-snapshot
Paleolatitudes in the Devonian of Brazil and the Frasnian-Famennian mass extinction-comments
inferred← citeshttps://doi.org/10.1016/0031-0182(78)90083-4openalex-snapshot
Silurian marine communities west of Dingle, Ireland
inferred← citeshttps://doi.org/10.1016/0031-0182(79)90089-0openalex-snapshot
Carbonate shelf environments and faunal communities in the Upper Bringewood Beds of the British Silurian
inferred← citeshttps://doi.org/10.1016/0031-0182(79)90099-3openalex-snapshot
The relative significance of depth and substrate in lower paleozoic community distributions
inferred← citeshttps://doi.org/10.1016/0031-0182(80)90002-4openalex-snapshot
A facies analysis of upper Ordovician regressive sequences in the Oslo Region, Norway — A record of glacio-eustatic changes
inferred← citeshttps://doi.org/10.1016/0031-0182(81)90068-7openalex-snapshot
Evolutionary replacement of ecological equivalents in Late Devonian benthic marine communities
inferred← citeshttps://doi.org/10.1016/0031-0182(83)90091-3openalex-snapshot
Environment of the Early Paleozoic vertebrates
inferred← citeshttps://doi.org/10.1016/0031-0182(84)90041-5openalex-snapshot
Destabilization of the oceanic density structure and its significance to marine “extinction” events
inferred← citeshttps://doi.org/10.1016/0031-0182(86)90094-5openalex-snapshot
Temporal change as an aspect of biogenic shell utilization and damage, Pleistocene of North Carolina, U.S.A
inferred← citeshttps://doi.org/10.1016/0031-0182(86)90135-5openalex-snapshot
Non-cryptic encrustation and pre-burial fracturing in stromatoporoids from the Upper Visby Beds of Gotland, Sweden
inferred← citeshttps://doi.org/10.1016/0031-0182(87)90036-8openalex-snapshot
Devonian palaeontological data and the Armorica problem
inferred← citeshttps://doi.org/10.1016/0031-0182(88)90054-5openalex-snapshot
Evolution of the freshwater ecosystem: The fossil record
inferred← citeshttps://doi.org/10.1016/0031-0182(88)90115-0openalex-snapshot
Ecological zonation during the carbonate transgression of a late Ordovician rocky shore (Northeastern Manitoba, Hudson Bay, Canada)
inferred← citeshttps://doi.org/10.1016/0031-0182(89)90067-9openalex-snapshot
Bathymetry and paleoecology of silurian bethic assemblages, late llandoverian, New York State
inferred← citeshttps://doi.org/10.1016/0031-0182(89)90163-6openalex-snapshot
Facies analysis and palaeogeography of the Rytteråker Formation (lower Silurian, Oslo region, Norway)
inferred← citeshttps://doi.org/10.1016/0031-0182(90)90209-popenalex-snapshot
Peripheral bulge of a foreland basin in the Oslo Region during the Early Silurian
inferred← citeshttps://doi.org/10.1016/0031-0182(91)90056-wopenalex-snapshot
Palaeoecology, taphonomy and distribution of brachiopod assemblages from the Much Wenlock Limestone Formation of England and Wales
inferred← citeshttps://doi.org/10.1016/0031-0182(93)90126-4openalex-snapshot
Middle Palaeozoic extinction events: Faunal and isotopic data
inferred← citeshttps://doi.org/10.1016/0031-0182(94)90113-9openalex-snapshot
A paleoclimate simulation of the Wenlockian (Late Early Silurian) world using a general circulation model with implications for early land plant paleoecology
inferred← citeshttps://doi.org/10.1016/0037-0738(90)90051-topenalex-snapshot
Sequences, cycles, and basin dynamics in the Silurian of the Appalachian Foreland Basin
inferred← citeshttps://doi.org/10.1016/0040-1951(90)90287-iopenalex-snapshot
Age of detrital zircon and titanite in the Meguma Group, southern Nova Scotia, Canada: Clues to the origin of the Meguma Terrane
inferred← citeshttps://doi.org/10.1016/0167-2789(95)00268-5openalex-snapshot
The spontaneous generation of digital “Life”
inferred← citeshttps://doi.org/10.1016/0169-5347(89)90163-8openalex-snapshot
Latitudinal gradients in species diversity
inferred← citeshttps://doi.org/10.1016/0377-8398(93)90011-lopenalex-snapshot
The Maastrichtian-Danian radiation of triserial and biserial planktic foraminifera: Testing phylogenetic and adaptational hypotheses in the (micro)fossil record
inferred← citeshttps://doi.org/10.1016/0895-9811(90)90026-wopenalex-snapshot
The basement of the Eastern Cordillera, Colombia: An allochthonous terrane in northwestern South America
inferred← citeshttps://doi.org/10.1016/b978-0-444-59425-9.00020-2openalex-snapshot
The Ordovician Period
inferred← citeshttps://doi.org/10.1016/j.actao.2013.08.005openalex-snapshot
Changes in seed rain across Atlantic Forest fragments in Northeast Brazil
inferred← citeshttps://doi.org/10.1016/j.earscirev.2006.01.001openalex-snapshot
Calibrating the Devonian Time Scale: A synthesis of U–Pb ID–TIMS ages and conodont stratigraphy
inferred← citeshttps://doi.org/10.1016/j.earscirev.2016.02.004openalex-snapshot
Gauging the impact of glacioeustasy on a mid-latitude early Silurian basin margin, mid Wales, UK
inferred← citeshttps://doi.org/10.1016/j.earscirev.2020.103280openalex-snapshot
The latest Ordovician Hirnantian brachiopod faunas: New global insights
inferred← citeshttps://doi.org/10.1016/j.earscirev.2023.104595openalex-snapshot
The rise and fall of the Malvinoxhosan (Malvinokaffric) bioregion in South Africa: Evidence for Early-Middle Devonian biocrises at the South Pole
inferred← citeshttps://doi.org/10.1016/j.geobios.2003.06.007openalex-snapshot
Upper Emsian Spinelloidea and Cyrtospiriferoidea (Brachiopoda, Spiriferidina) of the Cantabrian mountains (N Spain)
inferred← citeshttps://doi.org/10.1016/j.geobios.2019.07.004openalex-snapshot
Early Devonian (Lochkovian) trilobites and brachiopods from the west Balkhash Region, Kazakhstan and their significance for regional terrane dynamics
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2019.103069openalex-snapshot
Minor Δ33S anomalies coincide with biotic turnover events during the Great Ordovician Biodiversification Event (GOBE) in South China
inferred← citeshttps://doi.org/10.1016/j.gr.2017.08.006openalex-snapshot
Integrated record of Ludlow (Upper Silurian) oceanic geobioevents – Coordination of changes in conodont, and brachiopod faunas, and stable isotopes
inferred← citeshttps://doi.org/10.1016/j.gr.2020.06.002openalex-snapshot
Re-evaluating evidence of Australian eurypterids
inferred← citeshttps://doi.org/10.1016/j.jseaes.2004.09.005openalex-snapshot
The Devonian–Lower Carboniferous succession in Northwest Peninsular Malaysia
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.jseaes.2017.02.030openalex-snapshot
First report on the Early Devonian (Lochkovian) brachiopods from eastern Central Pamirs, Tajikistan
inferred← citeshttps://doi.org/10.1016/j.jseaes.2017.02.043openalex-snapshot
Brachiopod faunas after the end Ordovician mass extinction from South China: Testing ecological change through a major taxonomic crisis
inferred← citeshttps://doi.org/10.1016/j.lithos.2005.04.002openalex-snapshot
Evidence for the granulite–granite connection: Penecontemporaneous high-grade metamorphism, granitic magmatism and core complex development in the Liscomb Complex, Nova Scotia, Canada
inferred← citeshttps://doi.org/10.1016/j.palaeo.2004.05.013openalex-snapshot
Using GIS to unlock the interactions between biogeography, environment, and evolution in Middle and Late Devonian brachiopods and bivalves
inferred← citeshttps://doi.org/10.1016/j.palaeo.2004.06.019openalex-snapshot
Biodiversity dynamics and their driving factors during the Cretaceous diversification of Spatangoida (Echinoidea, Echinodermata)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2005.03.018openalex-snapshot
Paleobiogeographic patterns in the Middle and Late Devonian emphasizing Laurentia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2005.07.003openalex-snapshot
Assessing mechanisms of environmental change: Palynological signals across the Late Ludlow (Silurian) positive isotope excursion (δ13C, δ18O) on Gotland, Sweden
inferred← citeshttps://doi.org/10.1016/j.palaeo.2005.09.033openalex-snapshot
Erosion and deposition from bottom currents during the Givetian and Frasnian: Response to intensified oceanic circulation between Gondwana and Laurussia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2006.01.016openalex-snapshot
Replacements of benthic associations in a sequence stratigraphic framework, examples from Upper Ordovician of Sardinia and Lower Devonian of the Massif Armoricain
inferred← citeshttps://doi.org/10.1016/j.palaeo.2006.02.019openalex-snapshot
Preliminary report on the Late Ordovician graptolite extinction in the Yangtze region
inferred← citeshttps://doi.org/10.1016/j.palaeo.2007.05.023openalex-snapshot
Paleoecology of the Greater Phyllopod Bed community, Burgess Shale
inferred← citeshttps://doi.org/10.1016/j.palaeo.2009.03.007openalex-snapshot
Carbon isotopes and event stratigraphy near the Ordovician–Silurian boundary, Yichang, South China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2009.04.004openalex-snapshot
Silurian sequence stratigraphy of the Carnic Alps, Austria
inferred← citeshttps://doi.org/10.1016/j.palaeo.2010.03.046openalex-snapshot
Adaptive strategies in the evolution of encrusting tentaculitoid tubeworms
inferred← citeshttps://doi.org/10.1016/j.palaeo.2010.08.001openalex-snapshot
Ordovician and Silurian sea–water chemistry, sea level, and climate: A synopsis
inferred← citeshttps://doi.org/10.1016/j.palaeo.2010.10.008openalex-snapshot
Devonian sea-level change in Bolivia: A high palaeolatitude biostratigraphical calibration of the global sea-level curve
inferred← citeshttps://doi.org/10.1016/j.palaeo.2010.10.011openalex-snapshot
Precise position of the Basal Choteč event and evolution of sedimentary environments near the Lower–Middle Devonian boundary: The magnetic susceptibility, gamma-ray spectrometric, lithological, and geochemical record of the Prague Synform (Czech Republic)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2010.10.013openalex-snapshot
Late Eifelian (Middle Devonian) biocrises: Timing and signature of the pre-Kačák Bakoven and Stony Hollow Events in eastern North America
inferred← citeshttps://doi.org/10.1016/j.palaeo.2011.11.013openalex-snapshot
Palaeoecology of transported brachiopod assemblages embedded in black shale, Cape Phillips Formation (Silurian), Arctic Canada
inferred← citeshttps://doi.org/10.1016/j.palaeo.2012.01.009openalex-snapshot
Global palaeobiogeographical patterns in brachiopods from survival to recovery after the end-Ordovician mass extinction
inferred← citeshttps://doi.org/10.1016/j.palaeo.2013.02.027openalex-snapshot
Global palaeobiogeography of brachiopod faunas during the early Katian (Late Ordovician) greenhouse episode
inferred← citeshttps://doi.org/10.1016/j.palaeo.2015.09.001openalex-snapshot
Ordovician stable carbon isotope stratigraphy in the Tarim Basin, NW China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2015.11.024openalex-snapshot
Comparative study of Late Devonian (Famennian) brachiopod assemblages, sea level changes, and geo-events in northwestern and southern China
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.07.016openalex-snapshot
Post-extinction recovery and diversification of reef-dwelling brachiopod communities: Examples from the lower Silurian of Hudson Bay Basin, Canada
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.07.035openalex-snapshot
The highest-latitude Foliomena Fauna (Upper Ordovician, Portugal) and its palaeogeographical and palaeoecological significance
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.12.025openalex-snapshot
Post-extinction diversification patterns of brachiopods in the early–middle Llandovery, Silurian
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.04.026openalex-snapshot
The mid-Homerian (Silurian) biotic crisis in offshore settings of the Prague Synform, Czech Republic: Integration of the graptolite fossil record with conodonts, shelly fauna and carbon isotope data
inferred← citeshttps://doi.org/10.1016/j.palwor.2006.03.007openalex-snapshot
So-called background extinction rate is a sampling artifact
inferred← citeshttps://doi.org/10.1016/j.palwor.2009.05.002openalex-snapshot
Fossil plankton depth zones
inferred← citeshttps://doi.org/10.1016/j.palwor.2018.08.007openalex-snapshot
Palaeogeographic distribution and diversity of cephalopods during the Cambrian–Ordovician transition
inferred← citeshttps://doi.org/10.1016/j.palwor.2020.03.005openalex-snapshot
Givetian Stringocephalid brachiopods from eastern Yunnan of Southwest China with notes on global distribution of the family Stringocephalidae
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2003.12.009openalex-snapshot
Chitinozoan bio- and lithostratigraphical study of the Ashgill Fosses and Génicot Formations (Condroz Inlier, Belgium)
inferred← citeshttps://doi.org/10.1016/j.rgg.2007.11.015openalex-snapshot
Ordovician sea-level change and rapid change in crustal subsidence rates in East Siberia and Baltoscandia
inferred← citeshttps://doi.org/10.1016/j.tecto.2007.11.033openalex-snapshot
40Ar–39Ar white mica ages reveal Neoproterozoic/Paleozoic provenance and an Alleghanian overprint in coeval Upper Ordovician–Lower Devonian rocks of Meguma and Avalonia
inferred← citeshttps://doi.org/10.1016/s0012-8252(02)00105-8openalex-snapshot
Analysis and application of ichnofabrics
inferred← citeshttps://doi.org/10.1016/s0012-8252(02)00115-0openalex-snapshot
Palaeontological evidence bearing on global Ordovician–Silurian continental reconstructions
inferred← citeshttps://doi.org/10.1016/s0016-6995(01)80079-6openalex-snapshot
Late silurian marine shelly fauna of Central and Northern Vietnam
inferred← citeshttps://doi.org/10.1016/s0016-6995(09)90023-7openalex-snapshot
Les Bivalves Cyrtodontacea Ulrich 1894 de la Formation de York River, Emsien de Gaspésie, Québec
inferred← citeshttps://doi.org/10.1016/s0016-6995(09)90025-0openalex-snapshot
Une analyse multivariée appliquée au genre VandercammeninaBoucot, 1975 (Brachiopoda, Spiriferida) du Dévonien inférieur
inferred← citeshttps://doi.org/10.1016/s0016-6995(88)80030-5openalex-snapshot
La Formation du Faou (Dévonien inférieur du finistère):Nouvelles observations biostratigraphiques et mise en évidence d'une écozone
inferred← citeshttps://doi.org/10.1016/s0016-6995(99)80025-4openalex-snapshot
Energetics in the global marinefauna: A connection between terrestrial diversification and change in the marine biosphere
inferred← citeshttps://doi.org/10.1016/s0016-6995(99)80026-6openalex-snapshot
Organophosphatic brachiopods:Patterns of biodiversification and extinction in the Early Palaeozoic
inferred← citeshttps://doi.org/10.1016/s0016-7878(89)80068-9openalex-snapshot
The early Carboniferous (Courceyan) Middle Hope volcanics of Weston-super-Mare: development and demise of an offshore volcanic high
inferred← citeshttps://doi.org/10.1016/s0031-0182(00)00129-2openalex-snapshot
The Silurian Dicoelosia communities: temporal stability within an Ecologic Evolutionary Unit
inferred← citeshttps://doi.org/10.1016/s0031-0182(01)00274-7openalex-snapshot
Eurypterid palaeoecology: palaeobiological, ichnological and comparative evidence for a ‘mass–moult–mate’ hypothesis
inferred← citeshttps://doi.org/10.1016/s0031-0182(03)00736-3openalex-snapshot
Facies patterns and geography of the Yangtze region, South China, through the Ordovician and Silurian transition
inferred← citeshttps://doi.org/10.1016/s0031-0182(96)00064-8openalex-snapshot
Silurian Thalassinoides in an offshore carbonate community, Wisconsin, USA
inferred← citeshttps://doi.org/10.1016/s0031-0182(96)00085-5openalex-snapshot
Coordinated stasis: An overview
inferred← citeshttps://doi.org/10.1016/s0031-0182(96)00093-4openalex-snapshot
Coordinated stasis: biofacies revisited and the conceptual modeling of whole-fauna dynamics
inferred← citeshttps://doi.org/10.1016/s0031-0182(96)00094-6openalex-snapshot
Ecology of coordinated stasis
inferred← citeshttps://doi.org/10.1016/s0034-6667(97)00021-3openalex-snapshot
Biogeography of Late Silurian and Devonian acritarchs and prasinophytes
inferred← citeshttps://doi.org/10.1016/s0035-1598(96)90155-5openalex-snapshot
Dacryoconarides du genre Nowakia dans le praguien du bassin de prague (dévonien inférieur, République Tchèque)
inferred← citeshttps://doi.org/10.1016/s0040-1951(00)00038-xopenalex-snapshot
Relative sea-level changes in Baltoscandia in the Cumbrian and early Ordovician: the predominance of tectonic factors and the absence of large scale eustatic fluctuations
inferred← citeshttps://doi.org/10.1016/s0040-1951(97)00063-2openalex-snapshot
Correlations between the evolution of benthic faunal communities and convergent movements of lithospheric blocks from the Silurian to the Late Devonian in the mid-Palaeozoic Uralian basin
inferred← citeshttps://doi.org/10.1016/s0040-1951(97)00177-7openalex-snapshot
Late Devonian palinspastic reconstruction of the Avalon-Meguma terrane boundary: implications for terrane accretion and basin development in the Appalachian orogen
inferred← citeshttps://doi.org/10.1016/s0899-5362(99)00022-6openalex-snapshot
Southern African Phanerozoic marine invertebrates: Biogeography, pal˦oecology, climatology and comments on adjacent regions
inferred← citeshttps://doi.org/10.1016/s0920-5446(05)80005-6openalex-snapshot
Chapter 5 Devonian stromatoporoid originations, extinctions, and paleobiogeography: how they relate to the Frasnian-Famennian extinction
inferred← citeshttps://doi.org/10.1016/s1251-8050(00)01496-8openalex-snapshot
Relations entre les variations des assemblages benthiques emsiens et l'eustatisme dans la coupe de Seillou (Massif armoricain, France)
inferred← citeshttps://doi.org/10.1016/s1251-8050(98)80007-4openalex-snapshot
Communautés benthiques à Brachiopodes et variations eustatiques : exemple de la formation du Faou (Dévonien, Massif armoricain, France)
inferred← citeshttps://doi.org/10.1017/jpa.2017.121openalex-snapshot
Arthur James Boucot (1924–2017)
inferred← citeshttps://doi.org/10.1017/jpa.2017.74openalex-snapshot
Early athyride brachiopod evolution through the Ordovician-Silurian mass extinction and recovery, Anticosti Island, eastern Canada
inferred← citeshttps://doi.org/10.1017/jpa.2018.101openalex-snapshot
Bryozoan fauna from the Reynales Formation (lower Silurian, Aeronian) of New York, USA
inferred← citeshttps://doi.org/10.1017/jpa.2020.113openalex-snapshot
Schellwienella clarkei(Orthotetida, Brachiopoda): a new species from the Devonian of the Paraná Basin, Brazil
inferred← citeshttps://doi.org/10.1017/jpa.2020.27openalex-snapshot
Redescription, paleogeography, and experimental paleoecology of the Silurian phyllocaridGonatocaris
inferred← citeshttps://doi.org/10.1017/jpa.2021.74openalex-snapshot
HirnantiaFauna from the Condroz Inlier, Belgium: another case of a relict Ordovician shelly fauna in the Silurian?
inferred← citeshttps://doi.org/10.1017/jpa.2022.18openalex-snapshot
Rare stromatoporoids from the Lower Devonian (Emsian) of Nevada, and their biostratigraphic and paleobiogeographic significance
inferred← citeshttps://doi.org/10.1017/pab.2016.1openalex-snapshot
Biotic invasion, niche stability, and the assembly of regional biotas in deep time: comparison between faunal provinces
inferred← citeshttps://doi.org/10.1017/s001675680000844xopenalex-snapshot
Chronometric calibration of mid-Ordovician to Tournaisian conodont zones: a compilation from recent graphic-correlation and isotope studies
inferred← citeshttps://doi.org/10.1017/s0016756800014503openalex-snapshot
Upper Ordovician – lower Silurian sequences of the Bohemian Massif, central Europe
inferred← citeshttps://doi.org/10.1017/s0016756800025024openalex-snapshot
Implications for the age of South African Devonian rocks in which Tropidoleptus (Brachiopoda) has been found
inferred← citeshttps://doi.org/10.1017/s0016756800025486openalex-snapshot
Comments on the paper ‘Fission-track dating of British Ordovician and Silurian stratotypes’ by R. J. Ross and others
inferred← citeshttps://doi.org/10.1017/s0016756800033537openalex-snapshot
Age of the Cedarberg Formation, South Africa and early land plant evolution
inferred← citeshttps://doi.org/10.1017/s001675680005072xopenalex-snapshot
Range, proportionate representation, and demise of brachiopod families through Permian Period
inferred← citeshttps://doi.org/10.1017/s0016756802007070openalex-snapshot
Carbonate platform evolution and conodont stratigraphy during the middle Silurian Mulde Event, Gotland, Sweden
inferred← citeshttps://doi.org/10.1017/s0016756814000533openalex-snapshot
Integrated brachiopod-based bioevents and sequence-stratigraphic framework for a Late Ordovician subpolar platform, eastern Anti-Atlas, Morocco
inferred← citeshttps://doi.org/10.1017/s0016756897007802openalex-snapshot
Graptolite biostratigraphy of the Lower Silurian (Llandovery) shelf deposits of the Western Iberian Cordillera, Spain
inferred← citeshttps://doi.org/10.1017/s0022336000018369openalex-snapshot
The Ordovician brachiopod genusBimuriafrom the eastern Klamath Mountains, northern California
inferred← citeshttps://doi.org/10.1017/s0022336000019004openalex-snapshot
Trace fossils and depositional sequences in a clastic shelf setting, Upper Cretaceous of Utah
inferred← citeshttps://doi.org/10.1017/s0022336000019211openalex-snapshot
Tempestites recorded as variable Pentamerus layers in the Lower Silurian of southern Norway
inferred← citeshttps://doi.org/10.1017/s002233600002000xopenalex-snapshot
Lower and Middle Devonian brachiopod-dominated communities of Nevada, and their position in a biofacies-province-realm model
inferred← citeshttps://doi.org/10.1017/s0022336000021557openalex-snapshot
Origination, survivorship, and extinction of rudist taxa
inferred← citeshttps://doi.org/10.1017/s0022336000021636openalex-snapshot
The first fossiliferous Pridolian beds from the southern Appalachians in northern Alabama, and the age of the uppermost Red Mountain Formation
inferred← citeshttps://doi.org/10.1017/s0022336000021867openalex-snapshot
Biostratinomy of ostracode assemblages from a small reef flat in Maunalua Bay, Oahu, Hawaii
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