Journal of Paleontology

Papers
(The median citation count of Journal of Paleontology is 1. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2020-11-01 to 2024-11-01.)
ArticleCitations
Ectoparasite borings, mesoparasite borings, and scavenging traces in early Miocene turtle and tortoise shell: Moghra Formation, Wadi Moghra, Egypt21
New insights on the Early Pleistocene equids from Roca-Neyra (France, central Europe): implications for theHipparionLAD and theEquusFAD in Europe20
CeutorhynchusGermar (Coleoptera, Curculionidae) as proxy for Eocene core Brassicaceae: first record of the genus from Rovno amber19
Early Cambrian (Stage 4) brachiopods from the Shipai Formation in the Three Gorges area of South China16
The first records of mollusks from mid-Cretaceous Hkamti amber (Myanmar), with the description of a land snail, Euthema myanmarica n. sp. (Caenogastropoda, Cyclophoroidea, Diplommatinidae)15
Shale-hosted biota from the Dismal Lakes Group in Arctic Canada supports an early Mesoproterozoic diversification of eukaryotes15
A ten-faced hexangulaconulariid from Cambrian Stage 2 of South China15
The nasal cavity of two traversodontid cynodonts (Eucynodontia, Gomphodontia) from the Upper Triassic of Brazil14
Systematic paleontology, acritarch biostratigraphy, and δ13C chemostratigraphy of the early Ediacaran Krol A Formation, Lesser Himalaya, northern India13
Taxonomic revision of Ediacaran tubular fossils: Cloudina, Sinotubulites and Conotubus12
New records of injured Cambrian and Ordovician trilobites11
Ediacaran diversity and paleoecology from central Iran11
A new alligatoroid (Eusuchia, Crocodylia) from the Eocene of China and its implications for the relationships of Orientalosuchina10
The soft-bodied biota of the Cambrian Series 2 Parker Quarry Lagerstätte of northwestern Vermont, USA10
Articulated trilobite ontogeny: suggestions for a methodological standard10
Paleoecology of naticid–molluscan prey interaction during the Late Jurassic (Oxfordian) in Kutch, India: evolutionary implications9
A new bohaiornithid-like bird from the Lower Cretaceous of China fills a gap in enantiornithine disparity9
The Miocene fossil lizards from Kutch (Gujarat), India: a rare window to the past diversity of this subcontinent9
Paleontology and ichnology of the late Ediacaran Nasep–Huns transition (Nama Group, southern Namibia)8
New sphenodontian (Reptilia: Lepidosauria) from a novel Late Triassic paleobiota in western North America sheds light on the earliest radiation of herbivorous lepidosaurs8
Typhlocybinae leafhoppers (Hemiptera, Cicadellidae) from Eocene Rovno amber reveal a transition in wing venation and a defensive adaptation8
A new early-diverging sphenodontian (Lepidosauria, Rhynchocephalia) from the Upper Triassic of Virginia, U.S.A.7
An outer shelf shelly fauna from Cambrian Series 2 (Stage 4) of North Greenland (Laurentia)7
Carnivorous mammals from the middle Eocene Washakie Formation, Wyoming, USA, and their diversity trajectory in a post-warming world7
Description of the metoposauridAnaschisma brownifrom the New Oxford Formation of Pennsylvania7
A new titanopteranMagnatitan jongheonin. gen. n. sp. from southwestern Korean Peninsula7
Late Cretaceous sturgeons (Acipenseridae) from North America, with two new species from the Tanis site in the Hell Creek Formation of North Dakota7
New cynodonts (Therapsida, Eucynodontia) from the Late Triassic of India and their significances7
The oldest known record of a ground sloth (Mammalia, Xenarthra, Folivora) from Hispaniola: evolutionary and paleobiogeographical implications7
Diverse labechiid stromatoporoids from the Upper Ordovician Xiazhen Formation of South China and their paleobiogeographic implications7
A new species of Sclerocephalus with a fully ossified endocranium gives insight into braincase evolution in temnospondyls7
A new faunistic component of the Lower Triassic Panchet Formation of India increases the continental non-archosauromorph neodiapsid record in the aftermath of the end-Permian mass extinction7
Corynexochine trilobites of the Harkless Formation and Mule Spring Limestone (Cambrian Series 2, Stage 4), Clayton Ridge, Nevada7
Warm-waterTcherskidiumfauna (Brachiopoda) in the Late Ordovician Northern Hemisphere of Laurentia and peri-Laurentia7
A late Cisuralian (early Permian) brachiopod fauna from the Taungnyo Group in the Zwekabin Range, eastern Myanmar and its biostratigraphic, paleobiogeographic, and tectonic implications6
Ediacaran metazoan fossils with siliceous skeletons from the Digermulen Peninsula of Arctic Norway6
Lower Famennian (Upper Devonian) rhynchonellide and athyride brachiopods from the South Armenian Block6
New rhynchonellid and spire-bearing brachiopods from the Carboniferous of Mexico. Paleogeographical significance of the Oaxacan brachiopod fauna through the Serpukhovian–Moscovian6
“Ptychoparioid” trilobites of the Harkless Formation and Mule Spring Limestone (Cambrian Series 2, Stage 4), Clayton Ridge, Nevada6
Upside down: ‘Cryobatrachus’ and the lydekkerinid record from Antarctica5
The first documentation of an Ordovician eurypterid (Chelicerata) from China5
Deciduous dentition and dental eruption sequence in Interatheriinae (Notoungulata, Interatheriidae): implications in the systematics of the group5
Middle Ordovician (Whiterockian) gastropods from central Sonora, Mexico: affinities with Laurentia and the Precordillera5
Systematic paleontology of macroalgal fossils from the Tonian Mackenzie Mountains Supergroup5
Synchrotron imagery of phosphatized eggs in Waptia cf. W. fieldensis from the middle Cambrian (Miaolingian, Wuliuan) Spence Shale of Utah5
Biostratigraphy and taxonomy of fusulinid foraminifera across the Upper Mississippian (upper Serpukhovian)–Lower Pennsylvanian (Bashkirian) successions from the Hadim Nappe, Central Taurides, southern5
A new Early Triassic brachiopod fauna from southern Tibet, China: Implications on brachiopod recovery and the late Smithian extinction in southern Tethys5
A new cheilostome bryozoan from a dinosaur site in the Upper Cretaceous (Campanian) Judith River Formation of Montana5
Katian (Late Ordovician) conodonts on the northwestern margin of the North China Craton5
Middle Ordovician (middle Darriwilian) Archaeospicularia and Entactinaria (radiolarians) from the Table Cove Formation, Piccadilly Quarry, Newfoundland, Canada5
Amsassia(calcareous alga) from the Lower Ordovician (Tremadocian) of western Newfoundland, and the biologic affinity and geologic history of the genus5
Cornulitid tubeworms and other calcareous tubicolous organisms from the Hirmuse Formation (Katian, Upper Ordovician) of northern Estonia5
A probable skeleton ofIsisfordia(Crocodyliformes) and additional crocodyliform remains from the Griman Creek Formation (Cenomanian, New South Wales, Australia)4
Largest-known fossil penguin provides insight into the early evolution of sphenisciform body size and flipper anatomy4
Triassic Foraminifera from the Great Bank of Guizhou, Nanpanjiang Basin, south China: taxonomic account, biostratigraphy, and implications for recovery from end-Permian mass extinction4
Miocene instead of Jurassic: the importance of sound fieldwork for paleontological data analysis4
New Thylacocephala (Crustacea) assemblage from the Spathian (Lower Triassic) of Majiashan (Chaohu, Anhui Province, South China)4
An Early Devonian clam shrimp community from Hunan Province, China4
History of the Giraffe Pipe locality inferred from microfossil remains: a thriving freshwater ecosystem near the Arctic Circle during the warm Eocene4
Revision of Ordovician chitinozoan Lagenochitina esthonica sensu lato: morphometrics, biostratigraphy and paleobiogeography4
Grylloblattidan insects from Sperbersbach and Cabarz (Germany), two new early Permian and insect-rich localities4
Two new eurypterids (Arthropoda, Chelicerata) from the upper Silurian Yulongsi Formation of south-west China4
The rangeomorph fossil Charnia from the Ediacaran Shibantan biota in the Yangtze Gorges area, South China4
A new genus of treeshrew and other micromammals from the middle Miocene hominoid locality of Ramnagar, Udhampur District, Jammu and Kashmir, India4
Late Sandbian (Sa2) radiolarians of the Pingliang Formation from the Guanzhuang section, Gansu Province, China4
Adaptive function and phylogenetic significance of novel skeletal features of a new Devonian microconchid tubeworm (Tentaculita) from Wyoming, USA4
A new dissorophoid temnospondyl from the Allegheny Group (late Carboniferous) of Five Points, Mahoning County, Ohio (USA)4
Development of the early Cambrian oryctocephalid trilobiteOryctocarella duyunensisfrom western Hunan, China4
Geometric morphometric analysis for the systematic elucidation of new Hylicellidae from the Jurassic of China (Hemiptera: Cicadomorpha)4
Rhinocerotidae from the early Miocene of the Negev (Israel) and implications for the dispersal of early Neogene rhinoceroses4
Progress in understanding middle Eocene nassellarian (Radiolaria, Polycystinea) diversity; new insights from the western equatorial Atlantic Ocean4
Systematics of 12 Jurassic, Cretaceous, and Paleogene squat lobster taxa (Galatheoidea)4
A eurypterid trackway from the Middle Ordovician of New York State4
Lochkovian (Lower Devonian) conodonts from the Alengchu section, western Yunnan, China4
Pliocene fossils support a New Zealand origin for the smallest extant penguins3
Darriwilian (Middle Ordovician) new trilobites from the Upper Yangtze Region, South China, and their macroevolutionary and paleobiogeographic implications3
Arnebolagus, the oldest eulagomorph, and phylogenetic relationships within the Eocene Eulagomorpha new clade (Mammalia, Duplicidentata)3
OnCallavia(Trilobita) from the Cambrian Series 2 of Iberia with systematic status of the genus3
Nonmarine ostracod fauna from the Lower Cretaceous Shinekhudag Formation (southwest Mongolia): taxonomy, biostratigraphy, and paleoecology3
The termite genus Glyptotermes (Isoptera: Kalotermitidae) in Miocene amber from Ethiopia3
The first record of Hirnantian Ostracoda in South America: implications for the biostratigraphy and paleozoogeography of the Paraná basin3
The larval brachyopid Platycepsion wilkinsoni from the Triassic of New South Wales provides insight into the stereospondyl life cycle3
Crinoid calyx origin from stem radial echinoderms3
Rise of clathrodictyid stromatoporoids during the Great Ordovician Biodiversification Event: insights from the Upper Ordovician Xiazhen Formation of South China3
Araucariaceous fossil woods from the Upper Triassic Ischigualasto Formation (San Juan Province, Argentina): paleofloristic and paleoclimatic implications3
The smooth, spire-bearing brachiopods after the terminal Ordovician extinction through lower Llandovery in the central Oslo region, Norway3
Morphology and paleobiology of the Late Cretaceous large-sized sharkCretodus crassidens(Dixon, 1850) (Neoselachii; Lamniformes)3
The earliest example of sexual dimorphism in bivalves—evidence from the astartid Nicaniella (Lower Jurassic, southern Germany)3
An updated generic classification of Cenozoic pleurotomariid gastropods, with new records from the Oligocene and early Miocene of India3
Platymerella—a cool-water virgianid brachiopod fauna in southern Laurentia during the earliest Silurian3
New late Eocene and Oligocene plotopterid fossils from Washington State (USA), with a revision of “Tonsalabuchanani (Aves, Plotopteridae)3
Quaternary equatorial Atlantic deep-sea ostracodes: evidence for a distinct tropical fauna in the deep sea3
Paleotethyan faunal/floral evidence in the Mississippian Maritimes Basin of Canada: An overview3
A new, giant ricinuleid (Arachnida, Ricinulei), from the Pennsylvanian of Illinois, and the identification of a new, ontogenetically stable, diagnostic character3
Puercosuchus traverorum n. gen. n. sp.: a new malerisaurine azendohsaurid (Archosauromorpha: Allokotosauria) from two monodominant bonebeds in the Chinle Formation (Upper Triassic, Norian) of A3
Cavity-dwelling microorganisms from the Ediacaran and Cambrian of North Greenland (Laurentia)3
Feeding in the Devonian antiarch placoderm fishes: a study based upon morphofunctional analysis of jaws3
Three new cribrimorph bryozoans (order Cheilostomatida) from the early Miocene of Argentina, with a discussion on spinocystal shield morphologies3
The Inachoididae spider crabs (Crustacea, Brachyura) from the Neogene of the tropical Americas3
Revision ofHistiodella labiosaBauer, 2010, and its inferred phylogeny in the evolution of the Middle Ordovician conodont genusHistiodellaHarris, 19623
A new species ofHirnantia(Orthida, Brachiopoda) and its implications for the Hirnantian age of the Ellis Bay Formation, Anticosti Island, eastern Canada3
Micromammals from the late early Miocene of Çapak (western Anatolia) herald a time of change3
A new marrellomorph arthropod from southern Ontario: a rare case of soft-tissue preservation on a Late Ordovician open marine shelf3
The first Middle Ordovician and Gondwanan record of the cincinnaticrinid crinoidOhiocrinus byeongseonin. sp. from South Korea: biostratigraphy, paleobiogeography, and taphonomy3
Brachiopods from the Latham Shale Lagerstätte (Cambrian Series 2, Stage 4) and Cadiz Formation (Miaolingian, Wuliuan), California3
Rebuilding the foundation of late Paleozoic pinnid bivalve study (family Pinnidae)2
A novel antennal form in trilobites2
Crocodylian princess in Taiwan: Revising the taxonomic status of Tomistoma taiwanicus from the Pleistocene of Taiwan and its paleobiogeographic implications2
Evolutionary significance of the blastozoanEumorphocystisand its pseudo-arms2
New species of Liostracina Monke, 1903 (Trilobita, Cambrian) from Yunnan, China: complete holaspid exoskeleton and implications for higher level classification2
Organic-walled microfossils from the Ediacaran Sete Lagoas Formation, Bambuí Group, Southeast Brazil: taxonomic and biostratigraphic analyses2
The first Cretaceous ophiopluteus skeleton (Echinodermata: Ophiuroidea)2
First virtual endocast description of an early Miocene representative of Pan-Octodontoidea (Caviomorpha, Hystricognathi) and considerations on the early encephalic evolution in South American rodents2
New trilobite assemblage from the lower Cambrian (upper Stage 4) of the Lake Zone, western Mongolia2
The first discovery of Lochkovian (Lower Devonian) conodonts in central Guangxi, South China and its geological implications2
Early Miocene coral reef-associated bryozoans from Colombia. Part I: Cyclostomata, “Anasca” and Cribrilinoidea Cheilostomata2
Anatomy of the holotype of ‘Probelesodonkitchingi revisited, a chiniquodontid cynodont (Synapsida, Probainognathia) from the early Late Triassic of southern Brazil2
Problematic tubular fossils from the Portfjeld Formation (Ediacaran) of North Greenland2
New Middle Ordovician hyoliths from the Ossa Morena Zone, southwestern Spain2
Glossifungites gingrasi n. isp., a probable subaqueous insect domicile from the Cretaceous Ferron Sandstone, Utah2
New paromomyids (Mammalia, Primates) from the Paleocene of southwestern Alberta, Canada, and an analysis of paromomyid interrelationships2
Micro-CT analysis of Katian radiolarians from the Malongulli Formation, New South Wales, Australia, and implications for skeletogenesis2
New soft-bodied panarthropods from diverse Spence Shale (Cambrian; Miaolingian; Wuliuan) depositional environments2
BelinurusBronn, 1839 (Chelicerata, Xiphosura) has priority overBellinurusPictet, 18462
Characterization of the West Siberian lineage of zokors (Mammalia, Rodentia, Spalacidae, Myospalacinae) and divergence in molar development2
First report ofAcanthochaetetes(Porifera: Demospongiae) from the Cretaceous Khalsi Formation, Ladakh Himalaya, India2
Palliedaphichnium gondwanicumnew ichnogenus new ichnospecies, a millipede trace fossil from paleosols of the upper Permian Gondwana sequence of India2
New and revised cyrtospiriferid (Spiriferida) brachiopods from the lower Famennian (Upper Devonian) of Armenia2
Ancient Basidiomycota in an extinct conifer-like tree, Xenoxylon utahense, and a brief survey of fungi in the Upper Jurassic Morrison Formation, USA2
Ostracoda from the Santonian–Campanian (Upper Cretaceous) Nenjiang and Sifangtai formations, Songliao Basin, northeastern China2
Reptamsassia n. gen. (Amsassiaceae n. fam.; calcareous algae) from the Lower Ordovician (Floian) of western Newfoundland, and the earliest symbiotic intergrowth of modular species2
Elongate Ediacaran fronds from the Flinders Ranges, South Australia2
HirnantiaFauna from the Condroz Inlier, Belgium: another case of a relict Ordovician shelly fauna in the Silurian?2
Early Jurassic Trigoniida (Bivalvia) from Argentina2
Benthic foraminifera from the Albian shallow-marine limestones in the Geyik Dağı area (Central Taurides), southern Turkey2
A highly diverse dromioid crab assemblage (Decapoda, Brachyura) associated with pinnacle reefs in the lower Eocene of Spain2
Saetaspongia sponges from the Cambrian (Stage 4) Balang Formation of Guizhou, China2
Morphometric analysis of stem-group mollusks from the northern Yangtze Craton, China2
Not the first leech: An unusual worm from the early Silurian of Wisconsin2
A Glyptagnostus reticulatus trilobite faunule from the Cambrian of the Northern Qilian Mountains, northwest China, and its paleogeographical implications2
Early Miocene coral reef-associated bryozoans from Colombia. Part II: “Ascophora” Cheilostomatida2
The Paris Biota decapod (Arthropoda) fauna and the diversity of Triassic decapods2
Phylogeny and biogeography of some Cretaceous spatangoid echinoids with special emphasis on taxa from the Western Interior Seaway2
Cambrian (Stage 4 to Wuliuan) brachiopods from Sonora, Mexico2
A new genus and three new species of fossil braconid wasps (Hymenoptera, Ichneumonoidea) from Eocene Baltic and Rovno ambers2
New fossil remains of the commensal barnacleCryptolepas rhachianectiprovide evidence of gray whales in the prehistoric South Pacific2
Permian millipedes from the Fort Sill fissures of southwestern Oklahoma, with comments on allied taxa and millipedes preserved in karstic environments1
Wuchiapingian (Lopingian, late Permian) brachiopod fauna from Guangdong Province, southeastern China: systematics and contribution to the Lopingian recovery1
The first fossil record of the genus Phycosoma (Araneae, Theridiidae) from the lower Miocene Mexican amber, with the description of a new species1
Echericetus novellus n. gen. n. sp. (Cetacea, Mysticeti, Eomysticetidae), an Oligocene baleen whale from Baja California Sur, Mexico1
The late Pliensbachian (Early Jurassic) ammonoidAmaltheusin Japan: systematics and biostratigraphic and paleobiogeographic significance1
Corals and a cephalopod from the Whirlpool Formation (latest Ordovician, Hirnantian), Hamilton, Ontario: biostratigraphic and biogeographic significance1
Cribrilinid bryozoans from Pleistocene Mediterranean deep-waters, with the description of new species1
The dissorophoid temnospondyl Parioxys ferricolus from the early Permian (Cisuralian) of Texas1
Osteology and neuroanatomy of a phasianid (Aves: Galliformes) from the Miocene of Nebraska1
A new Late Devonian flora from Sonid Zuoqi, Inner Mongolia, northeastern China1
Revision of two Devonian cupressocrinitids from the Schultze collection (Museum of Comparative Zoology, Harvard University) and description of a newHalocrinites(Crinoidea, Eucladida)1
Cambrian trilobites from the Nounan Dolomite and lower St. Charles Formation (upper Marjuman to lower Sunwaptan; Miaolingian to Furongian Series), Smithfield Canyon, northern Utah1
Late CambrianPywackiais a cnidarian, not a bryozoan: Insights from skeletal microstructure1
New materials of acanthomorphic acritarchs from the Ediacaran Weng'an Biota (South China)1
Identification of the Oligocene to early Miocene loricariid catfish †Taubateia paraiba as a member of the Rhinelepinae1
The last representatives of the Superfamily Wellerelloidea (Brachiopoda, Rhynchonellida) in the westernmost Tethys (Iberian paleomargins) prior to their demise in the early Toarcian Mass Extinction Ev1
A possible Laurentian volchoviid ophiocistioid from the Katian of southwestern Ohio1
Middle Ordovician linguliformean microbrachiopods from western Argentina: new data and biogeographic implications1
Earliest western Atlantic staghorn corals (Acropora) from the lower Oligocene Suwannee Limestone of Florida, USA, and their significance for modern coral distribution1
Asian Paleocene charophyte records demonstrate Eocene dispersals from Asia to Europe – ERRATUM1
Microcomputed tomography of the holotype of the early tetrapodIchthyerpeton bradleyae(Huxley in Wright and Huxley, 1866) from the Pennsylvanian of Ireland1
Recognizing sponge inSpongiostromaGürich, 1906 from the Mississippian of Belgium1
Carnivorous reptile feeding strategies and postmortem food-processing behaviors: tooth traces on bones from the Upper Triassic Grabowa Formation (southern Poland)1
Earltonella fredricksi n. gen n. sp. and Thalassocystis striata (Chlorophyta, Bryopsidales) from the Silurian (Llandoverian) of the Timiskaming outlier, Ontario, Canada1
Cambrian trilobites from theGlossopleura walcottiZone (Miaolingian Series, Wuliuan Stage) of Mendoza, western Argentina1
Recovery of Laurentian cyclocystoids following Late Ordovician extinctions (Brassfield Formation, Llandovery; southwestern Ohio)1
A large pelagic lobopodian from the Cambrian Pioche Shale of Nevada1
Revision of Jurassic Protobranch Bivalves from Gebel Maghara, northern Sinai, Egypt1
Biostratigraphy and paleoecology of the trilobite faunas from the Mount Clark and Mount Cap formations (early and middle Cambrian), eastern Mackenzie Mountains, northwestern Canada1
Morphology, variation, and systematics of the late Cambrian Laurentian dikelocephalid trilobiteWalcottaspis vanhornei(Walcott, 1914)1
Bryozoans from the lower Silurian (Telychian) Hanchiatien Formation from southern Chongqing, South China1
Asian Paleocene charophyte records demonstrate Eocene dispersals from Asia to Europe1
Taxonomy and paleobiogeography of rudist bivalves from Upper Cretaceous strata, Gulf Coastal Plain and Puerto Rico, USA1
A new, complex hyaline larger benthic foraminifer, Bigaella orbitoidiformis n. gen. n. sp., from the upper Bartonian-Priabonian of NW Turkey1
First Report of Sphenothallus Hall (Cnidaria, Medusozoa) from the Mesozoic Erathem (Upper Triassic, Slovenia)1
Sympatric speciation driving evolution of Late Ordovician brachiopodZygospirain eastern North America1
Two Asian cricetodontine-like muroid rodents from the Neogene of western North America1
Variation in eye lenses of two new Late Devonian phacopid trilobites from western Junggar, NW China1
Systematics of the Early Ordovician (late Tremadocian; Stairsian) trilobiteGonioteloidesKobayashi, with species from the Great Basin, western USA1
Faunal and paleoenvironmental changes at a Cambrian (Jiangshanian; Steptoean–Sunwaptan boundary interval) trilobite extinction event, in contrasting deep- and shallow-subtidal settings, Nevada and Okl1
The first described fossil Oedemeridae (Insecta: Coleoptera) from Baltic amber1
Correcting a 135-year error: Limulidae Leach, 1819 (Chelicerata, Xiphosura) is the proper authority, not Limulidae Zittel, 18851
Evidence of large sturgeons in the Paleocene of North America1
Octocorals (Alcyonacea and Pennatulacea) from Paleogene deep-water strata in western Washington State, USA1
Phylogenetic positions of Paronychomys Jacobs and Basirepomys Korth and De Blieux relative to the tribe Neotomini (Rodentia, Cricetidae)1
A reappraisal of Nemavermes mackeei from the Mazon Creek fossil site expands Carboniferous cyclostome diversity1
Cambrian Age 3 small shelly fossils from the Terrades inlier, southern Pyrenees, Spain: Biostratigraphic and paleobiogeographic implications1
New paddlefishes (Acipenseriformes, Polyodontidae) from the Late Cretaceous Tanis Site of the Hell Creek Formation in North Dakota, USA1
A new species of the iconic triradial Ediacaran genus Tribrachidium from Nilpena Ediacara National Park, Flinders Ranges (South Australia)1
Biogeography of northeastern Atlantic Neogene chitons (Mollusca, Polyplacophora): New data from the Pliocene of Portugal1
Latest Ordovician to earliest Silurian graptolites of northwest Peninsular Malaysia1
Ostracoda from the Santonian–Campanian (Upper Cretaceous) Nenjiang and Sifangtai formations, Songliao Basin, northeastern China – Erratum1
One name to rule them all:Belinurus trilobitoides(Buckland, ) is senior synonym to fourteen named species1
Conulariid soft parts replicated in silica from the Scotch Grove Formation (lower Middle Silurian) of east-central Iowa1
The choanal anatomy of theSebecus icaeorhinusSimpson, 1937 and the variation of the palatine shape in notosuchians (Crocodyliformes, Mesoeucrocodylia)1
A partial tyrannosauroid femur from the mid-Cretaceous Wayan Formation of eastern Idaho, USA1
Spiracarneyella,a new carneyellid edrioasteroid from the Upper Ordovician (Katian) of Kentucky and Ohio and comments on carneyellid heterochrony1
Biogeographic, stratigraphic, and environmental distribution ofBasilosaurus(Mammalia, Cetacea) in North America with a review of the late Eocene shoreline in the southeastern coastal plain1
A new Cambrian (Jiangshanian, Sunwaptan) trilobite fauna from Oklahoma and its biostratigraphic significance.1
A new species Idiognathodus praeguizhouensis n. sp. (Conodonta, Pennsylvanian) from South China1
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