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An integrated study of echinoid taphonomy; predictions for the fossil record of four echinoid families
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00369023openalex-snapshot
Predation of the sea urchin Diadema antillarum Philippi on living coral
inferredcites →https://doi.org/10.1007/bf00372825openalex-snapshot
Foods and predators of the green sea urchin Strongylocentrotus droebachiensis in Newfoundland waters
inferredcites →https://doi.org/10.1016/0031-0182(88)90089-2openalex-snapshot
Fossilization potential of the mud crab, Panopeus (brachyura: Xanthidae) and temporal variability in crustacean taphonomy
inferredcites →https://doi.org/10.1017/s0016756800055850openalex-snapshot
Echinoid preservation in the Upper Estuarine Limestone of Blisworth, Northamptonshire
inferredcites →https://doi.org/10.1017/s0016756800077402openalex-snapshot
Asterozoa and the Study of Palaeozoic Faunas
inferredcites →https://doi.org/10.1017/s0094837300005248openalex-snapshot
The poor fossil record of the regular echinoid
inferredcites →https://doi.org/10.1017/s0094837300009982openalex-snapshot
Experimental disintegration of regular echinoids: roles of temperature, oxygen, and decay thresholds
inferredcites →https://doi.org/10.1017/s0094837300012215openalex-snapshot
Taphonomic bias and the evolutionary history of the family Cidaridae (Echinodermata: Echinoidea)
inferredcites →https://doi.org/10.1126/science.226.4672.335openalex-snapshot
Spread of Diadema Mass Mortality Through the Caribbean
inferredcites →https://doi.org/10.1130/0091-7613(1986)14<979:saitfr>2.0.co;2openalex-snapshot
Soft-bodied animals in the fossil record: The role of decay in fragmentation during transport
inferredcites →https://doi.org/10.1144/gsl.jgs.1927.083.01-05.23openalex-snapshot
The Occurrence, Structure, and Affinities of Echinocystis and Palæodiscus
inferredcites →https://doi.org/10.2307/3514691openalex-snapshot
Taphonomy of a modern shrimp; implicaions for the arthropod fossil record
inferredcites →https://doi.org/10.2307/3514692openalex-snapshot
Biostratinomy of Recent crinoids (Echinodermata) at Lizard Island, Great Barrier Reef, Australia
inferredcites →https://doi.org/10.3133/pp393aopenalex-snapshot
The Red Bird section of the Upper Cretaceous Pierre Shale in Wyoming
inferredcites →https://doi.org/10.5281/zenodo.16046014openalex-snapshot
Implications of lantern morphology for the phylogeny of post-Palaeozoic echinoids
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/zootaxa.4529.1.1zenodo-depositor-declared
Taxonomic guide and historical review of echinoids (Echinodermata: Echinoidea) from northeastern Brazil
inferred← citeshttps://doi.org/10.1002/bies.201700167openalex-snapshot
Soft‐Bodied Fossils Are Not Simply Rotten Carcasses – Toward a Holistic Understanding of Exceptional Fossil Preservation
inferred← citeshttps://doi.org/10.1002/gj.2783openalex-snapshot
Revision of echinoids from the Tournaisian (Mississippian) of Belgium and the importance of disarticulated material in assessing palaeodiversity
inferred← citeshttps://doi.org/10.1002/spp2.1280openalex-snapshot
Phylogenetic analysis of the Archaeocidaridae and Palaeozoic Miocidaridae (Echinodermata, Echinoidea) and the origin of crown group echinoids
inferred← citeshttps://doi.org/10.1007/978-1-4615-0161-9_12openalex-snapshot
Predation on Recent and Fossil Echinoids
inferred← citeshttps://doi.org/10.1007/978-94-017-7567-0_10openalex-snapshot
Living and Mineral Reefs: Are they Comparable and What Ecological Information Is Preserved?
inferred← citeshttps://doi.org/10.1007/bf00303429openalex-snapshot
Taphonomy of crown-of-thorns starfish: implications for recognizing ancient population outbreaks
inferred← citeshttps://doi.org/10.1007/s00338-005-0032-2openalex-snapshot
The fossil record of Diadema in the Caribbean
inferred← citeshttps://doi.org/10.1007/s00338-026-02847-6openalex-snapshot
Cryptic coral reef microhabitats and the functional role of brittle stars in biogenic sediment generation
inferred← citeshttps://doi.org/10.1007/s13358-018-0164-yopenalex-snapshot
A new fossil species of Clypeaster (Echinoidea) from Malaysian Borneo and an overview of the Central Indo-Pacific echinoid fossil record
inferred← citeshttps://doi.org/10.1016/j.earscirev.2015.01.009openalex-snapshot
Indirect paleo-seagrass indicators (IPSIs): A review
inferred← citeshttps://doi.org/10.1016/j.ibiod.2024.105904openalex-snapshot
Decay and preservation in marine basins: A guide to small multi-element skeletons
inferred← citeshttps://doi.org/10.1016/j.palaeo.2011.11.009openalex-snapshot
Taphonomic field experiments and the role of the Shelf and Slope Experimental Taphonomy Initiative
inferred← citeshttps://doi.org/10.1016/j.palaeo.2013.01.015openalex-snapshot
Multiple routes to mass accumulations of clypeasteroid echinoids: A comparative analysis of Miocene echinoid beds of Sardinia
inferred← citeshttps://doi.org/10.1016/j.palaeo.2013.06.023openalex-snapshot
Experimental tumbling of echinoderms — Taphonomic patterns and implications
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.03.024openalex-snapshot
Echinoid assemblages from the early Miocene of Funtanazza (Sardinia): A tool for reconstructing depositional environments along a shelf gradient
inferred← citeshttps://doi.org/10.1016/j.palaeo.2016.11.053openalex-snapshot
Palaeoecology and taphonomy of spatangoid-dominated echinoid assemblages: A case study from the Early-Middle Miocene of Sardinia, Italy
inferred← citeshttps://doi.org/10.1016/j.palaeo.2017.12.016openalex-snapshot
Evolutionary models in the Early Triassic marine realm
inferred← citeshttps://doi.org/10.1016/j.quageo.2016.12.001openalex-snapshot
Radiocarbon-calibrated amino acid racemization ages from Holocene sand dollars (Peronella peronii)
inferred← citeshttps://doi.org/10.1016/j.ympev.2016.07.028openalex-snapshot
Do genes lie? Mitochondrial capture masks the Red Sea collector urchin’s true identity (Echinodermata: Echinoidea: Tripneustes)
inferred← citeshttps://doi.org/10.1016/s0016-6995(94)80019-7openalex-snapshot
Taphonomie des Échinides dugisement de Cerin (kimméridgien Supérieur, Jura Méridional, France). Implications environnementales
inferred← citeshttps://doi.org/10.1016/s0031-0182(00)00208-xopenalex-snapshot
Evolution of Caribbean echinoderms during the Cenozoic: moving towards a complete picture using all of the fossils
inferred← citeshttps://doi.org/10.1016/s0031-0182(00)00209-1openalex-snapshot
Diversity patterns and biostratigraphy of Cenozoic echinoderms from Florida
inferred← citeshttps://doi.org/10.1016/s0031-0182(96)00055-7openalex-snapshot
Filtration models, guilds, and biofacies: Crinoid paleoecology of the Stanton Formation (Upper Pennsylvanian), midcontinent, North America
inferred← citeshttps://doi.org/10.1016/s0031-0182(96)00088-0openalex-snapshot
Crinoid biofacies in Upper Carboniferous cyclothems, midcontinent North America: faunal tracking and the role of regional processes in biofacies recurrence
inferred← citeshttps://doi.org/10.1016/s0031-0182(98)00210-7openalex-snapshot
Echinoid concentration beds: two examples from the stratigraphic spectrum
inferred← citeshttps://doi.org/10.1016/s0031-0182(98)00211-9openalex-snapshot
Taphonomic comparison between Recent and fossil sand dollars
inferred← citeshttps://doi.org/10.1017/9781108893374openalex-snapshot
Disarticulation and Preservation of Fossil Echinoderms: Recognition of Ecological-Time Information in the Echinoderm Fossil Record
inferred← citeshttps://doi.org/10.1017/jpa.2016.129openalex-snapshot
The role of preservation on the quantification of morphology and patterns of disparity within Paleozoic echinoderms
inferred← citeshttps://doi.org/10.1017/jpa.2016.46openalex-snapshot
Facies distribution and taphonomy of echinoids from the Fort Payne Formation (late Osagean, early Viséan, Mississippian) of Kentucky
inferred← citeshttps://doi.org/10.1017/jpa.2019.4openalex-snapshot
Paleoecology of sublittoral Miocene echinoids from Sardinia: A case study for substrate controls of faunal distributions
inferred← citeshttps://doi.org/10.1017/s0016756823000067openalex-snapshot
Mass occurrence of echinoids in an Oligocene hydrocarbon-seep limestone from the Olympic Peninsula, Washington State, USA
inferred← citeshttps://doi.org/10.1017/s0022336000022939openalex-snapshot
Pleistocene echinoid (Echinodermata) fauna from southeast Jamaica
inferred← citeshttps://doi.org/10.1017/s0094837300012215openalex-snapshot
Taphonomic bias and the evolutionary history of the family Cidaridae (Echinodermata: Echinoidea)
inferred← citeshttps://doi.org/10.1017/s1089332600000243openalex-snapshot
Echinoderm taphonomy, taphofacies, and Lagerstätten
inferred← citeshttps://doi.org/10.1017/s2475263000001094openalex-snapshot
Using numerical models to evaluate the consequences of time-averaging in marine fossil assemblages
inferred← citeshttps://doi.org/10.1017/s2475263000001148openalex-snapshot
Taphonomic approaches to temporal resolution in stratigraphy: Examples from Paleozoic marine mudrocks
inferred← citeshttps://doi.org/10.1080/00357529.1994.9925609openalex-snapshot
How to Fossilize a Sea Urchin
inferred← citeshttps://doi.org/10.1080/14772011003603556openalex-snapshot
The phylogeny and classification of post-Palaeozoic echinoids
inferred← citeshttps://doi.org/10.1111/ecog.02513openalex-snapshot
A 3000 year record of Caribbean reef urchin communities reveals causes and consequences of long‐term decline in Diadema antillarum
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1996.tb01870.xopenalex-snapshot
Taphonomic and sedimentologic implications of crinoid intraskeletal porosity
inferred← citeshttps://doi.org/10.1111/j.1502-3931.1999.tb00542.xopenalex-snapshot
Taphonomy of Clypeaster fragments: preservation and taphofacies
inferred← citeshttps://doi.org/10.1111/let.12090openalex-snapshot
The origin of echinoid shell beds in siliciclastic shelf environments: three examples from the Miocene of Sardinia, Italy
inferred← citeshttps://doi.org/10.1111/pala.12023openalex-snapshot
Experimentally observed soft‐tissue preservation near a marine brine seep
inferred← citeshttps://doi.org/10.1111/pala.70008openalex-snapshot
Taphonomic controls on a multi‐element marine skeletal fossil record
inferred← citeshttps://doi.org/10.1130/g39789.1openalex-snapshot
One fossil record, multiple time resolutions: Disparate time-averaging of echinoids and mollusks on a Holocene carbonate platform
inferred← citeshttps://doi.org/10.1130/g49970.1openalex-snapshot
Multiple phyla, one time resolution? Similar time averaging in benthic foraminifera, mollusk, echinoid, crustacean, and otolith fossil assemblages
inferred← citeshttps://doi.org/10.1139/cjz-79-7-1209openalex-snapshot
Not all written in stone: interdisciplinary syntheses in echinoderm paleontology
inferred← citeshttps://doi.org/10.15517/rbt.v65i1-1.31676openalex-snapshot
Procesos tafonómicos en una encrinita regional pensilvánica (Atokano), Sonora, México
inferred← citeshttps://doi.org/10.1666/10022.1openalex-snapshot
Changes in shell durability of common marine taxa through the Phanerozoic: evidence for biological rather than taphonomic drivers
inferred← citeshttps://doi.org/10.1666/13-130openalex-snapshot
First Record and Phylogenetic Significance of a Jurassic Diadematacean Sea Urchin from California
inferred← citeshttps://doi.org/10.1669/0883-1351(2001)016<0197:taedoh>2.0.co;2openalex-snapshot
Taphonomy and Environmental Distribution of Helicoplacoid Echinoderms
inferred← citeshttps://doi.org/10.1669/0883-1351(2002)017<0378:tspflt>2.0.co;2openalex-snapshot
The Stormy Path from Life to Death Assemblages: The Formation and Preservation of Mass Accumulations of Fossil Sand Dollars
inferred← citeshttps://doi.org/10.1669/0883-1351(2004)019<0017:abafct>2.0.co;2openalex-snapshot
A Bootstrap Analysis for Comparative Taphonomy Applied to Early Mississippian (Kinderhookian) Crinoids from the Wassonville Cycle of Iowa
inferred← citeshttps://doi.org/10.2110/palo.2005.p05-076ropenalex-snapshot
Contrast in Preservation of Bivalve Death Assemblages in Siliciclastic and Carbonate Tropical Shelf Settings
inferred← citeshttps://doi.org/10.2110/palo.2009.p09-144ropenalex-snapshot
POSSIBLE FOSSIL ECHINOID MASS MORTALITY DETECTED IN HOLOCENE LAGOONS, BELIZE
inferred← citeshttps://doi.org/10.2110/palo.2011.p11-015ropenalex-snapshot
ECHINODERM REMAINS IN SHALLOW-WATER CARBONATES AT FERNANDEZ BAY, SAN SALVADOR ISLAND, BAHAMAS
inferred← citeshttps://doi.org/10.2110/palo.2013.034openalex-snapshot
A PALEOECOLOGIC COMPARISON OF TWO EDRIOASTEROID (ECHINODERMATA) ENCRUSTED PAVEMENTS FROM THE UPPER ORDOVICIAN CORRYVILLE FORMATION OF FLORENCE, KENTUCKY AND THE MIAMITOWN SHALE OF SHARONVILLE, OHIO, U.S.A
inferred← citeshttps://doi.org/10.2110/palo.2014.087openalex-snapshot
THE ORIGIN AND PALEOECOLOGY OF CLYPEASTEROID ASSEMBLAGES FROM DIFFERENT SHELF SETTINGS OF THE MIOCENE OF SARDINIA, ITALY
inferred← citeshttps://doi.org/10.2110/palo.2017.041openalex-snapshot
FISH PREDATION ON A MEDITERRANEAN ECHINOID: IDENTIFICATION AND PRESERVATION POTENTIAL
inferred← citeshttps://doi.org/10.2110/palo.2018.046openalex-snapshot
PREDATION-FACILITATED PRESERVATION OF ECHINOIDS IN A TROPICAL MARINE ENVIRONMENT
inferred← citeshttps://doi.org/10.2110/palo.2019.024openalex-snapshot
COMPARATIVE TAPHONOMY OF DEEP-SEA AND SHALLOW-MARINE ECHINOIDS OF THE GENUS ECHINOCYAMUS
inferred← citeshttps://doi.org/10.22201/igl.05437652e.2012.1.1.134openalex-snapshot
Revisión de la aplicación de la tafonomía a los invertebrados bentónicos marinos (sin incluir artrópodos)
inferred← citeshttps://doi.org/10.2307/1542821openalex-snapshot
Structural Strengthening of Urchin Skeletons by Collagenous Sutural Ligaments
inferred← citeshttps://doi.org/10.2307/3515034openalex-snapshot
Is the fossil record of regular echinoids really so poor? A comparison of living and subfossil assemblages
inferred← citeshttps://doi.org/10.2307/3515136openalex-snapshot
Paleoecology of cool-water, subtidal cycles in mid-Cenozoic limestones, Eucla Platform, southern Australia
inferred← citeshttps://doi.org/10.2307/3515415openalex-snapshot
Census assemblages in hard-bottom coastal communities; a case study from the Plio-Pleistocene Mediterranean
inferred← citeshttps://doi.org/10.2478/agp-2014-0012openalex-snapshot
Badenian (Middle Miocene) echinoids and starfish from western Ukraine, and their biogeographic and stratigraphic significance
inferred← citeshttps://doi.org/10.2478/popore-2013-0010openalex-snapshot
First record of catacrinid crinoid from the Lower Permian of Spitsbergen
inferred← citeshttps://doi.org/10.2517/1342-8144(2008)12[145:eatsos]2.0.co;2openalex-snapshot
Ecological and taphonomic significance of spatangoid spines: relationship between mode of occurrence and water temperature
inferred← citeshttps://doi.org/10.26879/1090openalex-snapshot
Tracking biases in the regular echinoid fossil record: The case of Paracentrotus lividus in recent and fossil shallow-water, high-energy environments
inferred← citeshttps://doi.org/10.31223/x5gq5wopenalex-snapshot
Taphonomic Controls on a Multi-Element Skeletal Fossil Record
inferred← citeshttps://doi.org/10.7717/peerj.14245openalex-snapshot
Spatial distribution, diversity, and taphonomy of clypeasteroid and spatangoid echinoids of the central Florida Keys
inferred← citeshttps://doi.org/10.9719/eeg.2025.58.3.231openalex-snapshot
Brissopsis pohangensis sp. nov., a New Echinoid Species (Spatangoida) from the Middle Miocene Duho Formation, Pohang Basin, Korea
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