Journal of Paleontology

(The TQCC of Journal of Paleontology is 3. 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 2020-07-01 to 2024-07-01.)
A comprehensive anatomical and phylogenetic evaluation ofDilophosaurus wetherilli(Dinosauria, Theropoda) with descriptions of new specimens from the Kayenta Formation of northern Arizona36
New insights on the Early Pleistocene equids from Roca-Neyra (France, central Europe): implications for theHipparionLAD and theEquusFAD in Europe20
Ectoparasite borings, mesoparasite borings, and scavenging traces in early Miocene turtle and tortoise shell: Moghra Formation, Wadi Moghra, Egypt20
CeutorhynchusGermar (Coleoptera, Curculionidae) as proxy for Eocene core Brassicaceae: first record of the genus from Rovno amber19
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)16
Early Cambrian (Stage 4) brachiopods from the Shipai Formation in the Three Gorges area of South China15
The Ediacaran frondose fossil Arborea from the Shibantan limestone of South China15
Using three-dimensional geometric morphometric and dental topographic analyses to infer the systematics and paleoecology of fossil treeshrews (Mammalia, Scandentia)15
A ten-faced hexangulaconulariid from Cambrian Stage 2 of South China14
Shale-hosted biota from the Dismal Lakes Group in Arctic Canada supports an early Mesoproterozoic diversification of eukaryotes14
A new crocodylid from the middle Miocene of Kenya and the timing of crocodylian faunal change in the late Cenozoic of Africa13
Intravital damage to the body of Dickinsonia (Metazoa of the late Ediacaran)13
The nasal cavity of two traversodontid cynodonts (Eucynodontia, Gomphodontia) from the Upper Triassic of Brazil12
Systematic paleontology, acritarch biostratigraphy, and δ13C chemostratigraphy of the early Ediacaran Krol A Formation, Lesser Himalaya, northern India11
Ediacaran diversity and paleoecology from central Iran11
Articulated trilobite ontogeny: suggestions for a methodological standard10
New records of injured Cambrian and Ordovician trilobites9
Paleoecology of naticid–molluscan prey interaction during the Late Jurassic (Oxfordian) in Kutch, India: evolutionary implications9
Codium-like taxa from the Silurian of North America: morphology, taxonomy, paleoecology, and phylogenetic affinity9
A new alligatoroid (Eusuchia, Crocodylia) from the Eocene of China and its implications for the relationships of Orientalosuchina9
Early Miocene marine ostracodes from southwestern India: implications for their biogeography and the closure of the Tethyan Seaway9
Taxonomic revision of Ediacaran tubular fossils: Cloudina, Sinotubulites and Conotubus9
Trilobite fauna (Wuliuan Stage, Miaolingian Series, Cambrian) of the lower Lakeview Limestone, Pend Oreille Lake, Idaho8
Typhlocybinae leafhoppers (Hemiptera, Cicadellidae) from Eocene Rovno amber reveal a transition in wing venation and a defensive adaptation8
New sphenodontian (Reptilia: Lepidosauria) from a novel Late Triassic paleobiota in western North America sheds light on the earliest radiation of herbivorous lepidosaurs8
The Miocene fossil lizards from Kutch (Gujarat), India: a rare window to the past diversity of this subcontinent8
A new bohaiornithid-like bird from the Lower Cretaceous of China fills a gap in enantiornithine disparity8
New cynodonts (Therapsida, Eucynodontia) from the Late Triassic of India and their significances7
A new species of the gopherGregorymys(Rodentia, Geomyidae) from the early Oligocene (Arikareean 1) of southern Mexico7
The soft-bodied biota of the Cambrian Series 2 Parker Quarry Lagerstätte of northwestern Vermont, USA7
A new titanopteranMagnatitan jongheonin. gen. n. sp. from southwestern Korean Peninsula7
Corynexochine trilobites of the Harkless Formation and Mule Spring Limestone (Cambrian Series 2, Stage 4), Clayton Ridge, Nevada7
The oldest known record of a ground sloth (Mammalia, Xenarthra, Folivora) from Hispaniola: evolutionary and paleobiogeographical implications7
Paleontology and ichnology of the late Ediacaran Nasep–Huns transition (Nama Group, southern Namibia)7
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
Warm-waterTcherskidiumfauna (Brachiopoda) in the Late Ordovician Northern Hemisphere of Laurentia and peri-Laurentia7
Carnivorous mammals from the middle Eocene Washakie Formation, Wyoming, USA, and their diversity trajectory in a post-warming world7
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
Diversity and systematics of Middle-Late Ordovician calcified cyanobacteria and associated microfossils from Ordos Basin, North China7
Lower Famennian (Upper Devonian) rhynchonellide and athyride brachiopods from the South Armenian Block6
Redescription of †Yanosteus longidorsalis Jin et al., (Chondrostei, Acipenseriformes, †Peipiaosteidae) from the Early Cretaceous of China6
Diverse labechiid stromatoporoids from the Upper Ordovician Xiazhen Formation of South China and their paleobiogeographic implications6
Description of the metoposauridAnaschisma brownifrom the New Oxford Formation of Pennsylvania6
“Ptychoparioid” trilobites of the Harkless Formation and Mule Spring Limestone (Cambrian Series 2, Stage 4), Clayton Ridge, Nevada6
Amsassia(calcareous alga) from the Lower Ordovician (Tremadocian) of western Newfoundland, and the biologic affinity and geologic history of the genus5
A new Early Triassic brachiopod fauna from southern Tibet, China: Implications on brachiopod recovery and the late Smithian extinction in southern Tethys5
A new marine woodground ichnotaxon from the Lower Cretaceous Mannville Group, Saskatchewan, Canada5
Upside down: ‘Cryobatrachus’ and the lydekkerinid record from Antarctica5
First report of acrotretoid brachiopod shell beds in the lower Cambrian (Stage 4) Guanshan Biota of eastern Yunnan, South China5
Deciduous dentition and dental eruption sequence in Interatheriinae (Notoungulata, Interatheriidae): implications in the systematics of the group5
Late Cretaceous sturgeons (Acipenseridae) from North America, with two new species from the Tanis site in the Hell Creek Formation of North Dakota5
Middle Ordovician (middle Darriwilian) Archaeospicularia and Entactinaria (radiolarians) from the Table Cove Formation, Piccadilly Quarry, Newfoundland, Canada5
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
Microconchus cravenensisn. sp.: a giant among microconchid tubeworms5
A late Cisuralian (early Permian) brachiopod fauna from the Taungnyo Group in the Zwekabin Range, eastern Myanmar and its biostratigraphic, paleobiogeographic, and tectonic implications5
Plectatrypinae and other ribbed atrypides succeeding the end Ordovician extinction event, Central Oslo Region, Norway5
Atopidae (Trilobita) in the upper Marianian (Cambrian Series 2, Stage 4) of Iberia5
Systematic paleontology of macroalgal fossils from the Tonian Mackenzie Mountains Supergroup4
New Thylacocephala (Crustacea) assemblage from the Spathian (Lower Triassic) of Majiashan (Chaohu, Anhui Province, South China)4
Systematics of 12 Jurassic, Cretaceous, and Paleogene squat lobster taxa (Galatheoidea)4
Katian (Late Ordovician) conodonts on the northwestern margin of the North China Craton4
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
Ediacaran metazoan fossils with siliceous skeletons from the Digermulen Peninsula of Arctic Norway4
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
Early Miocene marsupialiforms, gymnures, and hedgehogs from Ribesalbes-Alcora Basin (Spain)4
An Early Devonian clam shrimp community from Hunan Province, China4
Lochkovian (Lower Devonian) conodonts from the Alengchu section, western Yunnan, China4
A probable skeleton ofIsisfordia(Crocodyliformes) and additional crocodyliform remains from the Griman Creek Formation (Cenomanian, New South Wales, Australia)4
Development of the early Cambrian oryctocephalid trilobiteOryctocarella duyunensisfrom western Hunan, China4
Cornulitid tubeworms and other calcareous tubicolous organisms from the Hirmuse Formation (Katian, Upper Ordovician) of northern Estonia4
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 rhynchonellid and spire-bearing brachiopods from the Carboniferous of Mexico. Paleogeographical significance of the Oaxacan brachiopod fauna through the Serpukhovian–Moscovian4
Late Sandbian (Sa2) radiolarians of the Pingliang Formation from the Guanzhuang section, Gansu Province, China4
A new dissorophoid temnospondyl from the Allegheny Group (late Carboniferous) of Five Points, Mahoning County, Ohio (USA)4
Late Miocene remains from Venta del Moro (Iberian Peninsula) provide further insights on the dispersal of crocodiles across the late Miocene Tethys4
A new cheilostome bryozoan from a dinosaur site in the Upper Cretaceous (Campanian) Judith River Formation of Montana4
Middle Ordovician (Whiterockian) gastropods from central Sonora, Mexico: affinities with Laurentia and the Precordillera4
The first record of Hirnantian Ostracoda in South America: implications for the biostratigraphy and paleozoogeography of the Paraná basin3
The rangeomorph fossil Charnia from the Ediacaran Shibantan biota in the Yangtze Gorges area, South China3
Progress in understanding middle Eocene nassellarian (Radiolaria, Polycystinea) diversity; new insights from the western equatorial Atlantic Ocean3
The larval brachyopid Platycepsion wilkinsoni from the Triassic of New South Wales provides insight into the stereospondyl life cycle3
New late Eocene and Oligocene plotopterid fossils from Washington State (USA), with a revision of “Tonsalabuchanani (Aves, Plotopteridae)3
Paleotethyan faunal/floral evidence in the Mississippian Maritimes Basin of Canada: An overview3
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
The earliest example of sexual dimorphism in bivalves—evidence from the astartid Nicaniella (Lower Jurassic, southern Germany)3
Adaptive function and phylogenetic significance of novel skeletal features of a new Devonian microconchid tubeworm (Tentaculita) from Wyoming, USA3
Symbiotic embedment structures in Silurian Caryocrinites (Echinodermata, Rhombifera, Hemicosmitida)3
Arnebolagus, the oldest eulagomorph, and phylogenetic relationships within the Eocene Eulagomorpha new clade (Mammalia, Duplicidentata)3
Largest-known fossil penguin provides insight into the early evolution of sphenisciform body size and flipper anatomy3
Three new cribrimorph bryozoans (order Cheilostomatida) from the early Miocene of Argentina, with a discussion on spinocystal shield morphologies3
Darriwilian (Middle Ordovician) new trilobites from the Upper Yangtze Region, South China, and their macroevolutionary and paleobiogeographic implications3
A new genus of treeshrew and other micromammals from the middle Miocene hominoid locality of Ramnagar, Udhampur District, Jammu and Kashmir, India3
Micromammals from the late early Miocene of Çapak (western Anatolia) herald a time of change3
The first Middle Ordovician and Gondwanan record of the cincinnaticrinid crinoidOhiocrinus byeongseonin. sp. from South Korea: biostratigraphy, paleobiogeography, and taphonomy3
The Inachoididae spider crabs (Crustacea, Brachyura) from the Neogene of the tropical Americas3
A eurypterid trackway from the Middle Ordovician of New York State3
The smooth, spire-bearing brachiopods after the terminal Ordovician extinction through lower Llandovery in the central Oslo region, Norway3
Quaternary equatorial Atlantic deep-sea ostracodes: evidence for a distinct tropical fauna in the deep sea3
Platymerella—a cool-water virgianid brachiopod fauna in southern Laurentia during the earliest Silurian3
A new marrellomorph arthropod from southern Ontario: a rare case of soft-tissue preservation on a Late Ordovician open marine shelf3
OnCallavia(Trilobita) from the Cambrian Series 2 of Iberia with systematic status of the genus3
An updated generic classification of Cenozoic pleurotomariid gastropods, with new records from the Oligocene and early Miocene of India3
Revision ofHistiodella labiosaBauer, 2010, and its inferred phylogeny in the evolution of the Middle Ordovician conodont genusHistiodellaHarris, 19623
The termite genus Glyptotermes (Isoptera: Kalotermitidae) in Miocene amber from Ethiopia3
Araucariaceous fossil woods from the Upper Triassic Ischigualasto Formation (San Juan Province, Argentina): paleofloristic and paleoclimatic implications3
Brachiopods from the Latham Shale Lagerstätte (Cambrian Series 2, Stage 4) and Cadiz Formation (Miaolingian, Wuliuan), California3
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
Nonmarine ostracod fauna from the Lower Cretaceous Shinekhudag Formation (southwest Mongolia): taxonomy, biostratigraphy, and paleoecology3
Two new eurypterids (Arthropoda, Chelicerata) from the upper Silurian Yulongsi Formation of south-west China3