Palaeontology

Papers
(The median citation count of Palaeontology 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 2022-01-01 to 2026-01-01.)
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Metamorphism as the cause of bone alteration in the Jarrow assemblage (Langsettian, Pennsylvanian) of Ireland25
Morphological disparity of mammalian limb bones throughout the Cenozoic: the role of biotic and abiotic factors23
Oldest winged insects: first Megasecoptera from the early Carboniferous (Serpukhovian) of Argentina21
Phyllosphere fungi of Middle Jurassic gymnosperms from Poland20
Decoding the drivers of deep‐time wetland biodiversity: insights from an early Permian tropical lake ecosystem18
Correction to ‘Ecological novelty at the start of the Cambrian and Ordovician radiations of echinoderms’17
Negative ontogenetic allometry of cardinal spines in the early Cambrian arthropod Isoxys volucris indicates their defensive function16
Preservational modes of some ichthyosaur soft tissues (Reptilia, Ichthyopterygia) from the Jurassic Posidonia Shale of Germany16
Plant dispersal in the Devonian world (c. 419–359 Ma)15
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Written in bones: palaeoclimate histotaphonomic history inferred from a complete Megatherium skeleton preserved in the Atacama Desert14
Bridging the extant and fossil record of planktonic foraminifera: implications for the Globigerina lineage14
Associations between trilobite intraspecific moulting variability and body proportions: Estaingia bilobata from the Cambrian Emu Bay Shale, Australia13
Standardizing fossil disparity metrics using sample coverage12
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Standing giants: a digital biomechanical model for bipedal postures in sauropod dinosaurs11
Sr‐O‐C isotope signatures reveal herbivore niche‐partitioning in a Cretaceous ecosystem11
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Fast production of large, time‐calibrated, informal supertrees with tree.merger11
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
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Putting the F into FBD analysis: tree constraints or morphological data?10
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The role of substrate in determining the dominance of immobile, epifaunal bivalves in the Late Cretaceous9
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The effects of sensitive environmental indicators in interpreting faunas of the past: a case study from the Jurassic of China9
Priapulid neoichnology, ecosystem engineering, and the Ediacaran–Cambrian transition8
Palaeobiology and taphonomy of the rangeomorph Culmofrons plumosa8
The endocast of Euparkeria sheds light on the ancestral archosaur nervous system8
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Locomotory and morphological evolution of the earliest Silurian graptolite Demirastrites selected by hydrodynamics8
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The many ways toward punctuated evolution7
Machine‐learning‐based morphological analyses of leaf epidermal cells in modern and fossil ginkgo and their implications for palaeoclimate studies7
Correction to ‘Establishing temperate crustose early Holocene coralline algae as archives for palaeoenvironmental reconstructions of the shallow water habitats of the Mediterranean Sea’7
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Microstructural and geochemical evidence offers a solution to the cephalopod cameral deposits riddle7
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Cranial endocast of Anagale gobiensis (Anagalidae) and its implications for early brain evolution in Euarchontoglires7
Functional morphology and biomechanics of an ontogenetic series of the Triassic cynodont Brasilodon quadrangularis and bite performance in the sister tax7
Deep origin of the crossed‐lamellar microstructure in early Cambrian molluscs6
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Relative skull size evolution in Mesozoic archosauromorphs: potential drivers and morphological uniqueness of erythrosuchid archosauriforms6
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 histology6
Gradual warming prior to the end‐Permian mass extinction6
High‐precision body mass predictors for small mammals: a case study in the Mesozoic6
Developmental models shed light on the earliest dental tissues, using Astraspis as an example6
Planetary‐scale change to the biosphere signalled by global species translocations can be used to identify the Anthropocene6
Paradox lost: wide gape in the Ordovician brachiopod Rafinesquina explains how unattached filter‐feeding strophomenoids thrived on muddy substrates6
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Climatic niche stability and lability in Holarctic non‐marine ostracods: implications for Quaternary palaeoclimate reconstruction5
Convergent evolution among non‐carnivorous, desert‐dwelling theropods as revealed by the dentary of the noasaurid Berthasaura leopoldinae (Cretaceous of Brazil)5
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The utility of probability plotting in palaeobiology5
Finite element and microstructural analyses indicate that pteraspid heterostracan oral plate microstructure was adapted to a mechanical function5
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Extraordinarily early Venus' flower basket sponges (Hexactinellida, Euplectellidae) from the uppermost Ordovician Anji Biota, China4
The conundrum of taxonomic uniformitarianism in planktic foraminifera4
Contrasting patterns of disparity suggest differing constraints on the evolution of trilobite cephalic structures during the Cambrian ‘explosion’4
Revealing the use of dental indices to infer taxonomic variation in sauropod dinosaurs4
A coherent biogeographical framework for Old World Neogene and Pleistocene mammals4
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Lasanius, an exceptionally preserved Silurian jawless fish from Scotland4
Initial quantitative assessment of the enigmatic clade Paracrinoidea (Echinodermata)4
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Ontogenetic trajectories of septal spacing and conch shape in the Late Cretaceous gaudryceratid ammonoids: implications for their post‐embryonic palaeoecology4
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Exceptions to the temperature–size rule: no Lilliput Effect in end‐Permian ostracods (Crustacea) from Aras Valley (northwest Iran)4
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 Revolution4
Pachyosteosclerosis, rhamphotheca and enhanced sensory capabilities of the premaxillae of Hyperodapedon (Archosauromorpha, Rhynchosauria): implications for foraging at the sediment–water interf3
Diversification dynamics of cheilostome bryozoans based on a Bayesian analysis of the fossil record3
Diversification and disparity in a major Palaeozoic clade of Brachiopoda: the rise and fall of the Plectambonitoidea3
How femoral morphology informs our understanding of the evolution of ornithopod locomotion and body size3
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Marine animal diversity across latitudinal and temperature gradients during the Phanerozoic3
ppgm: an R package for integrating neontological, palaeontological, and climate data in a phylogenetic comparative framework3
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On the estimation of body mass in temnospondyls: a case study using the large‐bodied Eryops and Paracyclotosaurus3
Ten simple rules to follow when cleaning occurrence data in palaeobiology3
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How does rapid burial work? New insights from experiments with echinoderms3
Ontogeny and evolution of the elasmosaurid neck highlight greater diversity of Antarctic plesiosaurians3
Down to earth: therian mammals became more terrestrial towards the end of the Cretaceous3
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Rise and fall of the phacopids: the morphological history of a successful trilobite family2
Analysing Thalattosuchia palaeobiodiversity through the prism of phylogenetic comparative methods2
A new insect boring in fossil wood from the Iranian Upper Cretaceous2
Morphological disparity and evolutionary rates of cranial and postcranial characters in sloths (Mammalia, Pilosa, Folivora)2
An efficient method for estimating vein density ofGlossopterisand its application2
How to date a crocodile: estimation of neosuchian clade ages and a comparison of four time‐scaling methods2
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Response of Mediterranean Sea bivalves to Pliocene–Pleistocene environmental changes2
Feeding habits of the Middle Triassic pseudosuchian Batrachotomus kupferzellensis from Germany and palaeoecological implications for archosaurs2
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Middle Pleistocene revelations: unravelling taphonomic processes in mammals including Mesotherium cristatum (Mesotheriidae, Notoungulata), Corralito Site, Córdoba Province, Argentina1
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For a while, crocodile: crocodylomorph resilience to mass extinctions1
Eocene palaeoenvironments and palaeoceanography of areas adjacent to the Drake Passage: insights from dinoflagellate cyst analysis1
Ventral organization of Jianfengia multisegmentalis Hou, and its implications for the head segmentation of megacheirans1
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Mouthpart morphology and feeding structures in the palaeocharinid trigonotarbids of the Rhynie chert: insights from comparisons to modern arachnids1
The origin and evolutionary history of necrophagy in Scarabaeinae (Coleoptera, Scarabaeidae): a comprehensive analysis of South American Coprinisphaera1
Understanding niche construction and phenotypic plasticity as causes of natural selection1
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How to engineer a habitable planet: the rise of marine ecosystem engineers through the Phanerozoic1
New anatomical details concerning the cranial structure of the early Permian stem reptile Protorothyris archeri revealed by μCT<1
Ecosystem engineers alter the evolution of seed size by impacting fertility and the understory light environment1
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