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The optimal acetate buffered acetic acid technique for extracting phosphatic fossils
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/0377-8398(88)90008-4openalex-snapshot
Conodonts investigative techniques and applications
inferredcites →https://doi.org/10.1017/s0022336000035319openalex-snapshot
A buffered formic acid technique for conodont extraction
inferredcites →https://doi.org/10.1080/02724634.1995.10011203openalex-snapshot
Revision of the Danian Cow Sharks, Sand Tiger Sharks, and Goblin Sharks (Hexanchidae, Odontaspididae, and Mitsukurinidae) from Southern Sweden
inferredcites →https://doi.org/10.1080/03115519908619339openalex-snapshot
A new technique to separate conodont elements from heavier minerals
inferredcites →https://doi.org/10.1111/j.1502-3931.1976.tb00970.xopenalex-snapshot
The Pander Society Newsletter
inferredcites →https://doi.org/10.1111/j.1502-3931.1994.tb01562.xopenalex-snapshot
Anatomy and phylogenetic significance of Eoconularia loculata, a conulariid from the Silurian of Gotland
inferredcites →https://doi.org/10.2307/1505838openalex-snapshot
Fossil Animal Remains: Their Preparation and Conservation
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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A Unitary Association-based conodont biozonation of the Smithian–Spathian boundary (Early Triassic) and associated biotic crisis from South China
inferred← citeshttps://doi.org/10.5852/ejt.2019.522zenodo-depositor-declared
Micro-computed tomography for natural history specimens: a handbook of best practice protocols
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/10.1002/gj.2425openalex-snapshot
New conodont species and biostratigraphy of the Santa Rosita Formation (upper Furongian–Tremadocian) in the Tilcara Range, Cordillera Oriental of Jujuy, Argentina
inferred← citeshttps://doi.org/10.1002/gj.2674openalex-snapshot
Late Wenlock carbon isotope excursions and associated conodont fauna in the Podlasie Depression, eastern Poland: a not‐so‐big crisis?
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Skeletal histology of Bothriolepis canadensis (Placodermi, Antiarchi) and evolution of the skeleton at the origin of jawed vertebrates
inferred← citeshttps://doi.org/10.1002/jmor.20997openalex-snapshot
The dermal skeleton of the jawless vertebrateTremataspis mammillata(Osteostraci, stem‐Gnathostomata)
inferred← citeshttps://doi.org/10.1002/spp2.1295openalex-snapshot
Brachiopods from the Byrd Group (Cambrian Series 2, Stage 4) Central Transantarctic Mountains, East Antarctica: biostratigraphy, phylogeny and systematics
inferred← citeshttps://doi.org/10.1002/spp2.1313openalex-snapshot
Small shelly fossils and carbon isotopes from the early Cambrian (Stages 3–4) Mural Formation of western Laurentia
inferred← citeshttps://doi.org/10.1002/spp2.1364openalex-snapshot
Silurian (late Llandovery – Wenlock) conodont fauna and biostratigraphy from the Yanbian area of Sichuan Province, south‐west China
inferred← citeshttps://doi.org/10.1002/spp2.1481openalex-snapshot
An expanded Smithian–Spathian (Lower Triassic) boundary from a reefal build‐up record in Oman: implications for conodont taxonomy, high‐resolution biochronology and the carbon isotope record
inferred← citeshttps://doi.org/10.1007/978-3-319-77401-5_2openalex-snapshot
Scientific Methods of Geological and Paleontological Collections and Trends in Paleontological Investigation and Research
inferred← citeshttps://doi.org/10.1007/978-90-481-3428-1_19openalex-snapshot
An Analysis of the Ireviken Event in the Boree Creek Formation, New South Wales, Australia
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/s00531-017-1572-8openalex-snapshot
Linking Palaeozoic palaeogeography of the Betic Cordillera to the Variscan Iberian Massif: new insight through the first conodonts of the Nevado-Filábride Complex
inferred← citeshttps://doi.org/10.1007/s12371-018-0310-3openalex-snapshot
How Do Fossilized Mammalian Bones Behave During Chemical Conservation? The Histological Case Studies of Tilos and Kerassia
inferred← citeshttps://doi.org/10.1007/s12542-025-00754-9openalex-snapshot
Re-evaluation of the Devonian ichthyofaunal assemblage from Lithuania and Belarus
inferred← citeshttps://doi.org/10.1007/s12549-017-0274-3openalex-snapshot
Palynology, microfacies and biostratigraphy across the Daleje Event (Lower Devonian, lower to upper Emsian): new insights from the offshore facies of the Prague Basin, Czech Republic
inferred← citeshttps://doi.org/10.1007/s12583-020-1392-9openalex-snapshot
Early Anisian (Middle Triassic) Conodonts from Romania and China, with Comments on Their Role in the Recognition and Correlation of the Base of the Anisian
inferred← citeshttps://doi.org/10.1007/s12594-017-0617-8openalex-snapshot
Techniques for Systematic Collection and Processing of Vertebrate Microfossils from their Host Mudrocks: A Case Study from the Upper Triassic Tiki Formation of India
inferred← citeshttps://doi.org/10.1007/s41513-020-00135-yopenalex-snapshot
A late Permian ichthyofauna from the Zechstein Basin, Lithuanian–Latvian Region
inferred← citeshttps://doi.org/10.1007/s41513-024-00274-6openalex-snapshot
Primary phosphate mineralization in mandibular elements of middle paleozoic archaeostracans from Spain
inferred← citeshttps://doi.org/10.1016/b978-0-12-824360-2.00003-6openalex-snapshot
Evolution and Biostratigraphy
inferred← citeshttps://doi.org/10.1016/j.apgeochem.2008.12.027openalex-snapshot
Rare earth element composition of Paleogene vertebrate fossils from Toadstool Geologic Park, Nebraska, USA
inferred← citeshttps://doi.org/10.1016/j.chemgeo.2015.08.025openalex-snapshot
A refined protocol for δ18OPO4 analysis of conodont bioapatite
inferred← citeshttps://doi.org/10.1016/j.chemgeo.2016.03.023openalex-snapshot
Effects of extraction protocols on the oxygen isotope composition of conodont elements
inferred← citeshttps://doi.org/10.1016/j.chemgeo.2018.06.026openalex-snapshot
Conodont thermochronology of exhumed footwalls of low-angle normal faults: A pilot study in the Mormon Mountains, Tule Springs Hills, and Beaver Dam Mountains, southeastern Nevada and southwestern Utah
inferred← citeshttps://doi.org/10.1016/j.chemgeo.2023.121761openalex-snapshot
REE + Y uptake in bioapatite revisited: Facies-controlled variability in coeval conodonts
inferred← citeshttps://doi.org/10.1016/j.conbuildmat.2018.04.142openalex-snapshot
Characterization of inner structure of limestone by X-ray computed sub-micron tomography
inferred← citeshttps://doi.org/10.1016/j.cretres.2013.04.002openalex-snapshot
Non-marine selachians from the basal Cretaceous of Charente, SW France
inferred← citeshttps://doi.org/10.1016/j.earscirev.2017.08.004openalex-snapshot
Agnostus pisiformis — a half a billion-year old pea-shaped enigma
inferred← citeshttps://doi.org/10.1016/j.earscirev.2018.11.003openalex-snapshot
Clade-dependent size response of conodonts to environmental changes during the late Smithian extinction
inferred← citeshttps://doi.org/10.1016/j.earscirev.2019.01.013openalex-snapshot
Dynamic interplay between climate and marine biodiversity upheavals during the early Triassic Smithian -Spathian biotic crisis
inferred← citeshttps://doi.org/10.1016/j.earscirev.2022.104017openalex-snapshot
Locating the BACE of the Cambrian: Bayan Gol in southwestern Mongolia and global correlation of the Ediacaran–Cambrian boundary
inferred← citeshttps://doi.org/10.1016/j.earscirev.2025.105157openalex-snapshot
The early Triassic time scale: New constraints from the Nanpanjiang Basin in South China and a review of geochronological, biostratigraphical and carbon isotope data
inferred← citeshttps://doi.org/10.1016/j.epsl.2016.10.003openalex-snapshot
Conodont (U–Th)/He thermochronology: A case study from the Illinois Basin
inferred← citeshttps://doi.org/10.1016/j.gca.2018.08.022openalex-snapshot
Controls of eustasy and diagenesis on the 238U/235U of carbonates and evolution of the seawater (234U/238U) during the last 1.4 Myr
inferred← citeshttps://doi.org/10.1016/j.geobios.2011.06.001openalex-snapshot
The elusive origin of Chiosella timorensis (Conodont Triassic)
inferred← citeshttps://doi.org/10.1016/j.geobios.2017.02.004openalex-snapshot
Pennsylvanian conodonts from the Tapajós Group (Amazonas Basin, Brazil)
inferred← citeshttps://doi.org/10.1016/j.geobios.2017.10.001openalex-snapshot
Conodont-based Griesbachian biochronology of the Guryul Ravine section (basal Triassic, Kashmir, India)
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2017.09.002openalex-snapshot
Time hierarchical analysis of the conodont paleocommunities and environmental change before and during the onset of the lower Silurian Mulde bioevent – A preliminary report
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2018.07.013openalex-snapshot
Early Wuchiapingian (Lopingian, late Permian) drowning event in the South China block suggests a late eruptive phase of Emeishan large Igneous Province
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2021.103613openalex-snapshot
Abundant conodont faunas from the Olenekian (Early Triassic) of subsurface British Columbia, Canada and diversification of the Neogondolellinae around the Smithian–Spathian boundary
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2025.105246openalex-snapshot
Oxygen isotope-based evidence for stepwise climate cooling aligns with the tripartite division of the Ordovician
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2026.105582openalex-snapshot
The early Silurian Valgu Glaciation and its effects on ocean chemistry and conodont faunal turnover
inferred← citeshttps://doi.org/10.1016/j.gr.2014.05.001openalex-snapshot
Life history and autecology of an Ediacaran index fossil: Development and dispersal of Cloudina
inferred← citeshttps://doi.org/10.1016/j.gr.2024.07.022openalex-snapshot
First multi-proxy chronostratigraphy of the lower Cambrian Byrd Group, Transantarctic Mountains and correlation within East Gondwana
inferred← citeshttps://doi.org/10.1016/j.gr.2025.02.028openalex-snapshot
Conodont diversity, biostratigraphy, and environmental dynamics: Unravelling the Smithian-Spathian transition at Guryul Ravine, Kashmir
inferred← citeshttps://doi.org/10.1016/j.jafrearsci.2024.105486openalex-snapshot
New insights from the Choteč Event (early Middle Devonian) in the Marhouma section (Ougarta range, SW Algeria)
inferred← citeshttps://doi.org/10.1016/j.jsames.2015.10.007openalex-snapshot
Conodont color alteration index and upper Paleozoic thermal history of the Amazonas Basin, Brazil
inferred← citeshttps://doi.org/10.1016/j.jsames.2024.105111openalex-snapshot
Darriwilian conodont biostratigraphy from the Rio Francia section, Central Precordillera, Argentina: A new insight into the Darriwilian conodont biozones
inferred← citeshttps://doi.org/10.1016/j.jseaes.2024.106077openalex-snapshot
Upper Cambrian and lower Ordovician conodont and carbon isotope bio-chemostratigraphy of the eastern North China Platform: Implications for global correlation and palaeoenvironments
inferred← citeshttps://doi.org/10.1016/j.marmicro.2023.102241openalex-snapshot
An endemic conodont fauna of Darriwilian (Middle Ordovician) age from the Santa Gertrudis Formation, southwestern Gondwanan margin and its paleobiogeographic relationships
inferred← citeshttps://doi.org/10.1016/j.marpetgeo.2018.05.018openalex-snapshot
Low-temperature thermochronology of Anticosti Island: A case study on the application of conodont (U-Th)/He thermochronology to carbonate basin analysis
inferred← citeshttps://doi.org/10.1016/j.micron.2005.05.005openalex-snapshot
X-ray microtomography of 410 million-year-old optic capsules from placoderm fishes
inferred← citeshttps://doi.org/10.1016/j.palaeo.2006.02.032openalex-snapshot
High-resolution Late Silurian correlations between Gotland, Sweden, and the Broken River region, NE Australia: Lithologies, conodonts and isotopes
inferred← citeshttps://doi.org/10.1016/j.palaeo.2012.11.018openalex-snapshot
Radiogenic isotope composition of Carboniferous seawater from North American epicontinental seas
inferred← citeshttps://doi.org/10.1016/j.palaeo.2013.11.021openalex-snapshot
The Cambrian–Ordovician transition in dysoxic facies in Baltica — diverse faunas and carbon isotope anomalies
inferred← citeshttps://doi.org/10.1016/j.palaeo.2015.08.020openalex-snapshot
Carbon cycling across the southern margin of Laurentia during the Late Ordovician
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.06.031openalex-snapshot
End-Wenlock terminal Mulde carbon isotope excursion in Gotland, Sweden: Integration of stratigraphy and taphonomy for correlations across restricted facies and specialized faunas
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.10.018openalex-snapshot
Assessing the fidelity of marine vertebrate microfossil δ18O signatures and their potential for palaeo-ecological and -climatic reconstructions
inferred← citeshttps://doi.org/10.1016/j.palaeo.2018.06.038openalex-snapshot
Heterogeneity of conodont faunas in the Cache Creek Terrane, Canada; significance for tectonic reconstructions of the North American Cordillera
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.01.028openalex-snapshot
Exceptional basal-body preservation in some Early Triassic conodont elements from Oman
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.05.022openalex-snapshot
Facies, phosphate, and fossil preservation potential across a Lower Cambrian carbonate shelf, Arrowie Basin, South Australia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2019.109449openalex-snapshot
Trace and rare earth element compositions of Silurian conodonts from the Vesiku Bone Bed: Histological and palaeoenvironmental implications
inferred← citeshttps://doi.org/10.1016/j.palaeo.2020.109806openalex-snapshot
Linked Silurian carbon cycle perturbations, bursts of pinnacle reef growth, extreme sea-level oscillations, and evaporite deposition (Michigan Basin, USA)
inferred← citeshttps://doi.org/10.1016/j.palaeo.2021.110347openalex-snapshot
Climate changes in the pre-Hirnantian Late Ordovician based on δ18Ophos studies from Estonia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2024.112034openalex-snapshot
Biosediment assemblages reveal disrupted silica cycling and redox conditions throughout the Rhaetian Stage: Evidence for a precursor event to the end-Triassic mass extinction
inferred← citeshttps://doi.org/10.1016/j.palaeo.2024.112378openalex-snapshot
Late Triassic (Norian) strontium and oxygen isotopes from the Baoshan block, southwestern China: Possible causes and implications for climate change
inferred← citeshttps://doi.org/10.1016/j.palaeo.2025.112740openalex-snapshot
New bio- and chemostratigraphic data from southwestern China and its relation to Telychian (Llandovery, Silurian) climate change
inferred← citeshttps://doi.org/10.1016/j.palaeo.2025.112765openalex-snapshot
Climate changes in the Middle and Late Ordovician of the tropical belt: The δ18O record from the Tunguska Basin of Siberia and its palaeogeographical relation
inferred← citeshttps://doi.org/10.1016/j.palaeo.2026.114061openalex-snapshot
Stratigraphic and geochemical insights into the glacioeustatic, tectonic, and diagenetic history of the upper Paleozoic Hermosa Group and lower Cutler beds, Paradox Basin, Utah, USA
inferred← citeshttps://doi.org/10.1016/j.palaeo.2026.114183openalex-snapshot
A Silurian volcanic island slope as an archive of mixed terrestrial and marine biota from the Prague Basin, Czech Republic: an integrated biochemostratigraphy and multiproxy analysis
inferred← citeshttps://doi.org/10.1016/j.palaeo.2026.114195openalex-snapshot
Fortunian small skeletal fossils and carbon isotope stratigraphy of the Bayangol Formation type section at Bayan Gol, southwestern Mongolia
inferred← citeshttps://doi.org/10.1016/j.palwor.2006.10.005openalex-snapshot
The ‘Orsten’—More than a Cambrian Konservat-Lagerstätte yielding exceptional preservation
inferred← citeshttps://doi.org/10.1016/j.palwor.2024.11.005openalex-snapshot
A new obolellid brachiopod from the Wirrealpa Limestone (Cambrian; Stage 4), Flinders Ranges, South Australia
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.2026.201173openalex-snapshot
High-resolution biostratigraphy across the Ordovician–Silurian transition in the Argentine Precordillera based on graptolite, conodont, and brachiopod data from the Jáchal area (San Juan Province, Argentina)
inferred← citeshttps://doi.org/10.1016/j.precamres.2015.06.013openalex-snapshot
Late Ediacaran skeletal body fossil assemblage from the Navalpino anticline, central Spain
inferred← citeshttps://doi.org/10.1016/j.tree.2014.04.004openalex-snapshot
A virtual world of paleontology
inferred← citeshttps://doi.org/10.1017/jpa.2016.119openalex-snapshot
New species of the conodontNeogondolellafrom the Anisian (Middle Triassic) of northeastern British Columbia, Canada, and their importance for regional correlation
inferred← citeshttps://doi.org/10.1017/jpa.2016.58openalex-snapshot
Early Devonian (Pragian) vertebrates from the northern Roberts Mountains, Nevada
inferred← citeshttps://doi.org/10.1017/jpa.2017.123openalex-snapshot
Magnigondolella, a new conodont genus from the Triassic of North America
inferred← citeshttps://doi.org/10.1017/jpa.2018.84openalex-snapshot
Mollusks from the upper Shackleton Limestone (Cambrian Series 2), Central Transantarctic Mountains, East Antarctica
inferred← citeshttps://doi.org/10.1017/jpa.2025.10164openalex-snapshot
A Cnidarian affinity for Salterella and Volborthella: implications for the evolution of shells
inferred← citeshttps://doi.org/10.1017/njg.2021.5openalex-snapshot
Note on the Rhaetian fish fauna from a subrosion pipe in Winterswijk (the Netherlands), with a discussion on the validity of the genus Severnichthys Storrs, 1994
inferred← citeshttps://doi.org/10.1017/njg.2023.10openalex-snapshot
Fish remains from the Rhaetian (Late Triassic) of Winterswijk, the Netherlands (Pisces: Chondrichthyes and Actinopterygii)
inferred← citeshttps://doi.org/10.1017/pab.2022.9openalex-snapshot
Sr/Ca and Ba/Ca ratios support trophic partitioning within a Silurian conodont community from Gotland, Sweden
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/s0016756809005962openalex-snapshot
Vagrant benthos (Annelida; Polychaeta) associated with Upper Ordovician carbonate mud-mounds of subsurface Gotland, Sweden
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/s0016756816000819openalex-snapshot
Darriwilian shallow-marine deposits from the Sultanate of Oman, a poorly known portion of the Arabian margin of Gondwana
inferred← citeshttps://doi.org/10.1017/s0016756817000589openalex-snapshot
Testing the early Late Ordovician cool-water hypothesis with oxygen isotopes from conodont apatite
inferred← citeshttps://doi.org/10.1017/s0016756820001260openalex-snapshot
Sedimentology and integrated chronostratigraphy of the lower Heatherdale Shale (Cambrian, stages 2–3), Stansbury Basin, South Australia
inferred← citeshttps://doi.org/10.1017/s0016756824000372openalex-snapshot
Stratigraphy and faunas of the Durness Group (Cambrian–Middle Ordovician) of Northwest Scotland: constraints on tectonic models and the development of the Great American Carbonate Bank
inferred← citeshttps://doi.org/10.1017/s0022336000039901openalex-snapshot
Silurian Ramphoprionid polychaetes from Gotland, Sweden
inferred← citeshttps://doi.org/10.1017/s0022336000044218openalex-snapshot
Late Ordovician jawed polychaete faunas of the type Cincinnatian region, U.S.A.
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/s1755691008007056openalex-snapshot
Morphology, evolution and stratigraphic distribution in the Middle Ordovician conodont genus Microzarkodina
inferred← citeshttps://doi.org/10.1017/s1755691023000051openalex-snapshot
The first Late Permian fish fossils from Leszczyna quarry in South-West Poland
inferred← citeshttps://doi.org/10.1038/ncomms14066openalex-snapshot
Refined Ordovician timescale reveals no link between asteroid breakup and biodiversification
inferred← citeshttps://doi.org/10.1039/d5tb01061fopenalex-snapshot
Silica substituted carbonate apatite: synthesis and analytical challenges
inferred← citeshttps://doi.org/10.1073/pnas.1901178116openalex-snapshot
Atmosphere–ocean oxygen and productivity dynamics during early animal radiations
inferred← citeshttps://doi.org/10.1080/00241160025100044openalex-snapshot
Enigmatic polychaete jaws from the Silurian of Gotland, Sweden
inferred← citeshttps://doi.org/10.1080/00241160050150195openalex-snapshot
Enrichment of metals in the jaws of fossil and extant polychaetes ‐ distribution and function
inferred← citeshttps://doi.org/10.1080/02724634.2016.1100632openalex-snapshot
Early Frasnian thelodont scales from central Iran and their implications for turiniid taxonomy, systematics and distribution
inferred← citeshttps://doi.org/10.1080/08120099.2025.2473098openalex-snapshot
Integrated biostratigraphy, chemostratigraphy and geochronology of the lower Cambrian succession in the western Stansbury Basin, South Australia
inferred← citeshttps://doi.org/10.1080/08912963.2021.1959577openalex-snapshot
A unique diversity hotspot for Polycopidae (Ostracoda) in the Triassic of North Dobrogea
inferred← citeshttps://doi.org/10.1080/08912963.2022.2131405openalex-snapshot
Actinopterygian and chondrichthyan ichthyoliths reveal enhanced cosmopolitanism in Late Triassic marine ecosystems
inferred← citeshttps://doi.org/10.1080/11035890401262221openalex-snapshot
Stratigraphical distribution of Campanian and Maastrichtian mosasaurs in Sweden – evidence of an intercontinental marine extinction event?
inferred← citeshttps://doi.org/10.1080/11035890401262231openalex-snapshot
Ytterholmen revisited – implications for the Late Wenlock stratigraphy of Gotland and coeval extinctions
inferred← citeshttps://doi.org/10.1080/11035890501274273openalex-snapshot
Conodont-based revisions of the Late Ludfordian on Gotland, Sweden
inferred← citeshttps://doi.org/10.1080/11035890701292117openalex-snapshot
ACordylodusfauna from the SW Gulf of Bothnia, Sweden
inferred← citeshttps://doi.org/10.1080/11035890801302079openalex-snapshot
An atypical intra-platform environment and biota from the Silurian of Gotland, Sweden
inferred← citeshttps://doi.org/10.1080/11035897.2010.496534openalex-snapshot
Mosasaur bite marks on a plesiosaur propodial from the Campanian (Late Cretaceous) of southern 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/10.1080/11035897.2012.704066openalex-snapshot
Kingnites diamondigen. et sp. nov., an exceptionally large Silurian paulinitid (Annelida; Polychaeta) from shallow marine settings of Baltoscandia
inferred← citeshttps://doi.org/10.1080/11035897.2018.1435561openalex-snapshot
Conodont biostratigraphy and carbon isotope stratigraphy of the Middle Ordovician (Darriwilian) Komstad Limestone, southern Sweden
inferred← citeshttps://doi.org/10.1080/11035897.2021.1895303openalex-snapshot
First discovery of Small Shelly Fossils and new occurrences of brachiopods and trilobites from the early Cambrian (Stage 4) of the Swedish Caledonides, Lapland
inferred← citeshttps://doi.org/10.1080/11035897.2025.2599542openalex-snapshot
Echinoderm limestone boulders from the Åland Islands, Finland (mid Sandbian, Ordovician) – earliest evidence of Baltscandian shallow water patch reefs
inferred← citeshttps://doi.org/10.1080/14772019.2014.963179openalex-snapshot
New hybodontiform and neoselachian sharks from the Lower Triassic of Oman
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/10.1080/14772019.2020.1794991openalex-snapshot
Ontogeny and evolutionary significance of a new acrotretide brachiopod genus from Cambrian Series 2 of South China
inferred← citeshttps://doi.org/10.1093/petrology/egaa003openalex-snapshot
The Fluorapatite P–REE–Th Vein Deposit at Nolans Bore: Genesis by Carbonatite Metasomatism
inferred← citeshttps://doi.org/10.1098/rsfs.2020.0015openalex-snapshot
Nucleus preservation in early Ediacaran Weng'an embryo-like fossils, experimental taphonomy of nuclei and implications for reading the eukaryote fossil record
inferred← citeshttps://doi.org/10.1101/554998openalex-snapshot
A late Permian ichthyofauna from the Zechstein Basin, Lithuania-Latvia Region
inferred← citeshttps://doi.org/10.1109/ted.2026.3712327openalex-snapshot
Performance Enhancement of AlGaInP-Based Red Mini-LEDs Through Acetic Acid Chemical Treatment
inferred← citeshttps://doi.org/10.1111/brv.12277openalex-snapshot
The origin of novel features by changes in developmental mechanisms: ontogeny and three‐dimensional microanatomy of polyodontode scales of two early osteichthyans
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2007.00690.xopenalex-snapshot
THE FIRST NEOCERATOPSIAN DINOSAUR REMAINS FROM EUROPE
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2008.00829.xopenalex-snapshot
A NEW METHOD FOR THE EXTRACTION OF MACROFOSSILS FROM CALCAREOUS ROCKS USING SULPHURIC ACID
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2009.00915.xopenalex-snapshot
Morphological criteria for recognising homology in isolated skeletal elements: comparison of traditional and morphometric approaches in conodonts
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2010.00967.xopenalex-snapshot
Neoselachian sharks from the Callovian-Oxfordian (Jurassic) of Ogrodzieniec, Zawiercie Region, southern Poland
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2011.01108.xopenalex-snapshot
Acid treatment effects on the stable isotopic signatures of fossils
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2012.01148.xopenalex-snapshot
New palaeoscolecid worms from the Furongian (upper Cambrian) of Hunan, South China: isMarkueliaan embryonic palaeoscolecid?
inferred← citeshttps://doi.org/10.1111/j.1475-4983.2012.01199.xopenalex-snapshot
A new diverse shark fauna from the Wordian (Middle Permian) Khuff Formation in the interior Haushi‐Huqf area, Sultanate of Oman
inferred← citeshttps://doi.org/10.1111/j.1525-142x.2006.00093.xopenalex-snapshot
Fossilized embryos are widespread but the record is temporally and taxonomically biased
inferred← citeshttps://doi.org/10.1111/let.12137openalex-snapshot
Faunal and facies changes through the mid Homerian (late Wenlock, Silurian) positive carbon isotope excursion in Podolia, western Ukraine
inferred← citeshttps://doi.org/10.1111/let.12149openalex-snapshot
Baring it all: undressing Cambrian ‘Orsten’ phosphatocopine crustaceans using synchrotron radiation X-ray tomographic microscopy
inferred← citeshttps://doi.org/10.1111/let.12160openalex-snapshot
Butterflies of the Cambrian benthos? Shield position in bradoriid arthropods
inferred← citeshttps://doi.org/10.1111/let.12172openalex-snapshot
Palaeozoic ‘conodont pearls’ and other phosphatic micro-spherules
inferred← citeshttps://doi.org/10.1111/let.12281openalex-snapshot
New data from Oman indicate benthic high biomass productivity coupled with low taxonomic diversity in the aftermath of the Permian–Triassic Boundary mass extinction
inferred← citeshttps://doi.org/10.1111/pala.12079openalex-snapshot
Crossing the boundary: an elasmobranch fauna from S tevns K lint, D enmark
inferred← citeshttps://doi.org/10.1111/pala.12162openalex-snapshot
Conodonts from the E arly T riassic microbialite of G uangxi ( S outh C hina): implications for the definition of the base of the T riassic S ystem
inferred← citeshttps://doi.org/10.1111/pala.12326openalex-snapshot
Harnessing stratigraphic bias at the section scale: conodont diversity in the Homerian (Silurian) of the Midland Platform, England
inferred← citeshttps://doi.org/10.1111/sed.12041openalex-snapshot
Stratal architecture and platform evolution of an early Frasnian syn‐tectonic carbonate platform, Canning Basin, Australia
inferred← citeshttps://doi.org/10.1111/ter.12068openalex-snapshot
Frasnian–Famennian crisis in the Malaguide Complex (Betic Cordillera, Spain)
inferred← citeshttps://doi.org/10.1126/sciadv.aar5690openalex-snapshot
An early Cambrian greenhouse climate
inferred← citeshttps://doi.org/10.1130/b36317.1openalex-snapshot
A composite Llandovery δ13Ccarb record from the Michigan Basin, USA
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/10.1130/g25461a.1openalex-snapshot
Syndepositional fault control on lower Frasnian platform evolution, Lennard Shelf, Canning Basin, Australia
inferred← citeshttps://doi.org/10.1139/cjes-2015-0091openalex-snapshot
Silurian conodont biostratigraphy and carbon (δ13Ccarb) isotope stratigraphy of the Victor Mine (V-03-270-AH) core in the Moose River Basin
inferred← citeshttps://doi.org/10.1139/cjes-2015-0223openalex-snapshot
Biochemostratigraphy of the Eramosa Formation in southwestern Ontario, Canada
inferred← citeshttps://doi.org/10.1144/0016-76492011-048openalex-snapshot
Oxygen isotope variability in conodonts: implications for reconstructing Palaeozoic palaeoclimates and palaeoceanography
inferred← citeshttps://doi.org/10.1144/jmpaleo2015-005openalex-snapshot
An integrated microwave technique for releasing microfossils from an indurated bone bed
inferred← citeshttps://doi.org/10.1186/s13358-020-00205-9openalex-snapshot
Sedimentary organic matter from a cored Early Triassic succession, Georgetown (Idaho, USA)
inferred← citeshttps://doi.org/10.1186/s13358-025-00377-2openalex-snapshot
New ichthyofaunal microfossils from the Late Permian at Chaotian, Sichuan, Southwest China
inferred← citeshttps://doi.org/10.1371/journal.pone.0035625openalex-snapshot
Exceptionally Preserved Cambrian Trilobite Digestive System Revealed in 3D by Synchrotron-Radiation X-Ray Tomographic Microscopy
inferred← citeshttps://doi.org/10.1371/journal.pone.0042582openalex-snapshot
Internal Soft-Tissue Anatomy of Cambrian ‘Orsten’ Arthropods as Revealed by Synchrotron X-Ray Tomographic Microscopy
inferred← citeshttps://doi.org/10.1371/journal.pone.0071890openalex-snapshot
Scales and Tooth Whorls of Ancient Fishes Challenge Distinction between External and Oral ‘Teeth’
inferred← citeshttps://doi.org/10.1515/agp-2015-0003openalex-snapshot
Upper Devonian microvertebrates from the Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.1515/popore-2015-0015openalex-snapshot
Crinoids from Svalbard in the aftermath of the end−Permian mass extinction
inferred← citeshttps://doi.org/10.1666/0022-3360(2001)075<0993:srpfgs>2.0.co;2openalex-snapshot
SILURIAN RAMPHOPRIONID POLYCHAETES FROM GOTLAND, SWEDEN
inferred← citeshttps://doi.org/10.1666/0022-3360(2003)077<0509:lojpfo>2.0.co;2openalex-snapshot
LATE ORDOVICIAN JAWED POLYCHAETE FAUNAS OF THE TYPE CINCINNATIAN REGION, U.S.A
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(2005)079[0763:hsasmw]2.0.co;2openalex-snapshot
HALISAURUS STERNBERGI, A SMALL MOSASAUR WITH AN INTERCONTINENTAL DISTRIBUTION
inferred← citeshttps://doi.org/10.1666/0022-3360(2005)079[0997:tfpdft]2.0.co;2openalex-snapshot
THE FIRST PACHYCEPHALOSAURINE (DINOSAURIA) FROM THE PALEO-ARCTIC OF ALASKA AND ITS PALEOGEOGRAPHIC IMPLICATIONS
inferred← citeshttps://doi.org/10.1666/0022-3360(2005)079[1157:tfrohr]2.0.co;2openalex-snapshot
THE FIRST RECORD OF HAINOSAURUS (REPTILIA: MOSASAURIDAE) FROM SWEDEN
inferred← citeshttps://doi.org/10.1666/13-038openalex-snapshot
A complete reconstruction of the hyolithid skeleton
inferred← citeshttps://doi.org/10.1666/pleo06-009.1openalex-snapshot
EARLY DEVONIAN (EMSIAN) ACANTHODIAN FAUNAS OF THE WESTERN USA
inferred← citeshttps://doi.org/10.1671/1928openalex-snapshot
A redescription ofAtopacanthus dentatusHussakof and Bryant, 1918 (Acanthodii, Ischnacanthidae)
inferred← citeshttps://doi.org/10.18261/let.57.2.3openalex-snapshot
Spatiotemporal dynamics of nektonic biodiversity and vegetation shifts during the Smithian–Spathian transition: conodont and palynomorph insights from Svalbard
inferred← citeshttps://doi.org/10.19110/2221-1381-2018-10-30-34openalex-snapshot
The Early Silurian Ozarkodina kozhimica group (Conodonta) from the Subpolar Urals
inferred← citeshttps://doi.org/10.2110/palo.2014.105openalex-snapshot
TAPHONOMIC BIAS OF SELECTIVE SILICIFICATION REVEALED BY PAIRED PETROGRAPHIC AND INSOLUBLE RESIDUE ANALYSIS
inferred← citeshttps://doi.org/10.2139/ssrn.6023609openalex-snapshot
Stratigraphic and geochemical insights into the glacioeustatic, tectonic, and diagenetic history of the Late Paleozoic Hermosa Group and lower Cutler beds, Paradox Basin, Utah, USA
inferred← citeshttps://doi.org/10.21701/bolgeomin.131.4.018openalex-snapshot
A geological and biostratigraphic study of the Paleozoic of the Malaguide Complex in the Cogollos Vega Zone (Granada) using conodonts
inferred← citeshttps://doi.org/10.2475/04.2016.03openalex-snapshot
Dynamics of abundance of the mid- to late Pridoli conodonts from the eastern part of the Silurian Baltic basin: Multifractals, state shifts, and oscillations
inferred← citeshttps://doi.org/10.26879/382openalex-snapshot
An acid-free method of microfossil extraction from clay-rich lithologies using the surfactant Rewoquat
inferred← citeshttps://doi.org/10.26879/583openalex-snapshot
Late Devonian and Early Carboniferous chondrichthyans from the Fairfield Group, Canning Basin, Western Australia
inferred← citeshttps://doi.org/10.26879/730openalex-snapshot
The oldest record of gnathostome fossils from Greece: Chondrichthyes from the Lopingian of Hydra Island
inferred← citeshttps://doi.org/10.29041/strat.10.3.01openalex-snapshot
Paleozoic stratigraphy of the Longi-Taormina Unit (PeloritanianMountains, southern Italy)
inferred← citeshttps://doi.org/10.29041/strat.17.3.205-212openalex-snapshot
Successful complete digestion of well lithified shale and extraction of microfossils from Devonian beds in western New York
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/10.3176/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/earth.2014.01openalex-snapshot
The Llandovery–Wenlock boundary interval in west-central continental Estonia: an example from the Suigu (S-3) core section; pp. 1–17
inferred← citeshttps://doi.org/10.3176/earth.2020.03openalex-snapshot
Middle Ordovician carbonate facies development, conodont biostratigraphy and faunal diversity patterns at the Lynna River, northwestern Russia
inferred← citeshttps://doi.org/10.3176/earth.2020.05openalex-snapshot
The lower boundary of the Haljala Regional Stage (Sandbian, Upper Ordovician) in Estonia; pp. 76–90
inferred← citeshttps://doi.org/10.3176/earth.2023.52openalex-snapshot
Boundary between the Porkuni and Juuru regional stages in the Neitla section, Estonia
inferred← citeshttps://doi.org/10.3389/feart.2023.1220590openalex-snapshot
The utility of the Upper Triassic conodont Primatella in Tethyan-Panthalassan correlation around the Carnian-Norian boundary
inferred← citeshttps://doi.org/10.3390/d16050276openalex-snapshot
A Description of the New Hybodont Shark Genus, Columnaodus, from the Burlington and Keokuk Limestones (Carboniferous, Mississippian, Osagean) of Illinois and Iowa, USA
inferred← citeshttps://doi.org/10.3390/fossils2030007openalex-snapshot
Middle Devonian actinopterygians from Lithuania and Belarus
inferred← citeshttps://doi.org/10.37570/bgsd-2005-52-03openalex-snapshot
Dental and vertebral morphology of the enigmatic mosasaur Dollosaurus (Reptilia, Mosasauridae) from the lower Campanian (Upper Cretaceous) of southern Sweden
inferred← citeshttps://doi.org/10.3906/yer-1612-29openalex-snapshot
Higher-resolution biostratigraphy for the Kinta Limestone and an implication for continuous sedimentation in the Paleo-Tethys, Western Belt of Peninsular Malaysia
inferred← citeshttps://doi.org/10.3989/egeol.43012.470openalex-snapshot
Una biota transicional Ediacárica–Cámbrica en el anticlinal de Abenójar (Macizo Ibérico, España)
inferred← citeshttps://doi.org/10.4202/app.00758.2020openalex-snapshot
Camenellan tommotiids from the Cambrian Series 2 of East Antarctica: biostratigraphy, palaeobiogeography, and systematics
inferred← citeshttps://doi.org/10.4202/app.00839.2020openalex-snapshot
Late Permian ichthyofauna from the North-Sudetic Basin, SW Poland
inferred← citeshttps://doi.org/10.4202/app.2012.0123openalex-snapshot
Neoselachians from the Danian (Early Paleocene) of Denmark
inferred← citeshttps://doi.org/10.5194/jm-43-283-2024openalex-snapshot
Cambrian Furongian–Middle Ordovician conodonts in the northeastern margin of the South China Block (Chuzhou, Anhui province) and their paleogeographic implications
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