Palaeontology

Papers
(The median citation count of Palaeontology is 2. 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 2021-08-01 to 2025-08-01.)
ArticleCitations
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Morphological disparity of mammalian limb bones throughout the Cenozoic: the role of biotic and abiotic factors22
Decoding the drivers of deep‐time wetland biodiversity: insights from an early Permian tropical lake ecosystem21
Metamorphism as the cause of bone alteration in the Jarrow assemblage (Langsettian, Pennsylvanian) of Ireland18
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Postcrania of Borealestes (Mammaliformes, Docodonta) and the emergence of ecomorphological diversity in early mammals16
Preservational modes of some ichthyosaur soft tissues (Reptilia, Ichthyopterygia) from the Jurassic Posidonia Shale of Germany15
Dinosaurian survivorship schedules revisited: new insights from an age‐structured population model15
Plant dispersal in the Devonian world (c. 419–359 Ma)14
Correction to ‘Ecological novelty at the start of the Cambrian and Ordovician radiations of echinoderms’14
Written in bones: palaeoclimate histotaphonomic history inferred from a complete Megatherium skeleton preserved in the Atacama Desert13
A new proteid salamander (Urodela, Proteidae) from the middle Miocene of Hambach (Germany) and implications for the evolution of the family13
Negative ontogenetic allometry of cardinal spines in the early Cambrian arthropod Isoxys volucris indicates their defensive function13
Bridging the extant and fossil record of planktonic foraminifera: implications for the Globigerina lineage12
Stuck in the mud: experimental taphonomy and computed tomography demonstrate the critical role of sediment in stabilizing the three‐dimensional external morphology of arthropod carcasses during early 11
Crypsis in the pelagic realm: evidence from exceptionally preserved fossil fish larvae from the Eocene Stolleklint Clay of Denmark11
Standardizing fossil disparity metrics using sample coverage11
Associations between trilobite intraspecific moulting variability and body proportions: Estaingia bilobata from the Cambrian Emu Bay Shale, Australia11
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Putting the F into FBD analysis: tree constraints or morphological data?10
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Sr‐O‐C isotope signatures reveal herbivore niche‐partitioning in a Cretaceous ecosystem10
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Fast production of large, time‐calibrated, informal supertrees with tree.merger9
Standing giants: a digital biomechanical model for bipedal postures in sauropod dinosaurs9
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The endocast of Euparkeria sheds light on the ancestral archosaur nervous system8
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Palaeobiology and taphonomy of the rangeomorph Culmofrons plumosa7
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Correction to ‘Establishing temperate crustose early Holocene coralline algae as archives for palaeoenvironmental reconstructions of the shallow water habitats of the Mediterranean Sea’7
Locomotory and morphological evolution of the earliest Silurian graptolite Demirastrites selected by hydrodynamics7
Validating marine Devonian biogeography: a study in bioregionalization7
Cranial endocast of Anagale gobiensis (Anagalidae) and its implications for early brain evolution in Euarchontoglires7
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Priapulid neoichnology, ecosystem engineering, and the Ediacaran–Cambrian transition7
The many ways toward punctuated evolution7
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Machine‐learning‐based morphological analyses of leaf epidermal cells in modern and fossil ginkgo and their implications for palaeoclimate studies6
Deep origin of the crossed‐lamellar microstructure in early Cambrian molluscs6
Developmental models shed light on the earliest dental tissues, using Astraspis as an example6
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High‐precision body mass predictors for small mammals: a case study in the Mesozoic6
Paradox lost: wide gape in the Ordovician brachiopod Rafinesquina explains how unattached filter‐feeding strophomenoids thrived on muddy substrates6
Gradual warming prior to the end‐Permian mass extinction6
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The utility of probability plotting in palaeobiology5
Convergent evolution among non‐carnivorous, desert‐dwelling theropods as revealed by the dentary of the noasaurid Berthasaura leopoldinae (Cretaceous of Brazil)5
Phylogenetic sampling affects evolutionary patterns of morphological disparity5
Relative skull size evolution in Mesozoic archosauromorphs: potential drivers and morphological uniqueness of erythrosuchid archosauriforms5
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I believe I can fly… New implications for the mode of life and palaeoecology of the Late Triassic Ozimek volans based on its unique long bone histology5
Planetary‐scale change to the biosphere signalled by global species translocations can be used to identify the Anthropocene5
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Revealing the use of dental indices to infer taxonomic variation in sauropod dinosaurs4
Lasanius, an exceptionally preserved Silurian jawless fish from Scotland4
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Finite element and microstructural analyses indicate that pteraspid heterostracan oral plate microstructure was adapted to a mechanical function4
A coherent biogeographical framework for Old World Neogene and Pleistocene mammals4
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Ontogenetic trajectories of septal spacing and conch shape in the Late Cretaceous gaudryceratid ammonoids: implications for their post‐embryonic palaeoecology4
The conundrum of taxonomic uniformitarianism in planktic foraminifera4
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Extraordinarily early Venus' flower basket sponges (Hexactinellida, Euplectellidae) from the uppermost Ordovician Anji Biota, China4
How does rapid burial work? New insights from experiments with echinoderms4
Marine animal diversity across latitudinal and temperature gradients during the Phanerozoic3
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Down to earth: therian mammals became more terrestrial towards the end of the Cretaceous3
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Exceptions to the temperature–size rule: no Lilliput Effect in end‐Permian ostracods (Crustacea) from Aras Valley (northwest Iran)3
Human face‐off: a new method for mapping evolutionary rates on three‐dimensional digital models3
Diversification and disparity in a major Palaeozoic clade of Brachiopoda: the rise and fall of the Plectambonitoidea3
How long does a brachiopod shell last on a seafloor? Modern mid‐bathyal environments as taphonomic analogues of continental shelves prior to the Mesozoic Marine Revolution3
Contrasting patterns of disparity suggest differing constraints on the evolution of trilobite cephalic structures during the Cambrian ‘explosion’3
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Pachyosteosclerosis, rhamphotheca and enhanced sensory capabilities of the premaxillae of Hyperodapedon (Archosauromorpha, Rhynchosauria): implications for foraging at the sediment–water interf3
Initial quantitative assessment of the enigmatic clade Paracrinoidea (Echinodermata)3
How femoral morphology informs our understanding of the evolution of ornithopod locomotion and body size2
An efficient method for estimating vein density ofGlossopterisand its application2
Response of Mediterranean Sea bivalves to Pliocene–Pleistocene environmental changes2
Middle Pleistocene revelations: unravelling taphonomic processes in mammals including Mesotherium cristatum (Mesotheriidae, Notoungulata), Corralito Site, Córdoba Province, Argentina2
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Ventral organization of Jianfengia multisegmentalis Hou, and its implications for the head segmentation of megacheirans2
Slow and fast evolutionary rates in the history of lepidosaurs2
Diversification dynamics of cheilostome bryozoans based on a Bayesian analysis of the fossil record2
On the estimation of body mass in temnospondyls: a case study using the large‐bodied Eryops and Paracyclotosaurus2
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Mouthpart morphology and feeding structures in the palaeocharinid trigonotarbids of the Rhynie chert: insights from comparisons to modern arachnids2
Feeding habits of the Middle Triassic pseudosuchian Batrachotomus kupferzellensis from Germany and palaeoecological implications for archosaurs2
Rise and fall of the phacopids: the morphological history of a successful trilobite family2
How to date a crocodile: estimation of neosuchian clade ages and a comparison of four time‐scaling methods2
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Ontogeny and evolution of the elasmosaurid neck highlight greater diversity of Antarctic plesiosaurians2
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Understanding niche construction and phenotypic plasticity as causes of natural selection2
Morphological disparity and evolutionary rates of cranial and postcranial characters in sloths (Mammalia, Pilosa, Folivora)2
Analysing Thalattosuchia palaeobiodiversity through the prism of phylogenetic comparative methods2
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