Palaeontology

Papers
(The TQCC of Palaeontology is 5. 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 2022-06-01 to 2026-06-01.)
ArticleCitations
37
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Metamorphism as the cause of bone alteration in the Jarrow assemblage (Langsettian, Pennsylvanian) of Ireland29
Morphological disparity of mammalian limb bones throughout the Cenozoic: the role of biotic and abiotic factors28
Oldest winged insects: first Megasecoptera from the early Carboniferous (Serpukhovian) of Argentina24
Phyllosphere fungi of Middle Jurassic gymnosperms from Poland20
Decoding the drivers of deep‐time wetland biodiversity: insights from an early Permian tropical lake ecosystem20
Plant dispersal in the Devonian world (c. 419–359 Ma)19
Preservational modes of some ichthyosaur soft tissues (Reptilia, Ichthyopterygia) from the Jurassic Posidonia Shale of Germany19
Negative ontogenetic allometry of cardinal spines in the early Cambrian arthropod Isoxys volucris indicates their defensive function19
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Correction to ‘Ecological novelty at the start of the Cambrian and Ordovician radiations of echinoderms’17
Written in bones: palaeoclimate histotaphonomic history inferred from a complete Megatherium skeleton preserved in the Atacama Desert16
Associations between trilobite intraspecific moulting variability and body proportions: Estaingia bilobata from the Cambrian Emu Bay Shale, Australia14
Bridging the extant and fossil record of planktonic foraminifera: implications for the Globigerina lineage14
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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 13
Phylogenetically‐informed estimates of notosuchian (Archosauria, Crocodylomorpha) body size and the challenges of inferring macroevolutionary patterns in extinct groups12
Standardizing fossil disparity metrics using sample coverage12
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Putting the F into FBD analysis: tree constraints or morphological data?11
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Standing giants: a digital biomechanical model for bipedal postures in sauropod dinosaurs11
Extinction risk related to functional traits in Pliocene to Holocene West Atlantic molluscs10
How should I publish my digital fossil? Recommendations for the publication of comprehensive 3D datasets in palaeontological studies10
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The role of substrate in determining the dominance of immobile, epifaunal bivalves in the Late Cretaceous10
The effects of sensitive environmental indicators in interpreting faunas of the past: a case study from the Jurassic of China10
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The endocast of Euparkeria sheds light on the ancestral archosaur nervous system8
Palaeobiology and taphonomy of the rangeomorph Culmofrons plumosa8
Priapulid neoichnology, ecosystem engineering, and the Ediacaran–Cambrian transition8
Locomotory and morphological evolution of the earliest Silurian graptolite Demirastrites selected by hydrodynamics8
7
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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
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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
The many ways toward punctuated evolution7
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
Microstructural and geochemical evidence offers a solution to the cephalopod cameral deposits riddle6
Deep origin of the crossed‐lamellar microstructure in early Cambrian molluscs6
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Climatic niche stability and lability in Holarctic non‐marine ostracods: implications for Quaternary palaeoclimate reconstruction5
Corrigendum to ‘Oldest evidence of a weasel reveals a Miocene origin of the Mustelinae (Mammalia, Carnivora)’5
Convergent evolution among non‐carnivorous, desert‐dwelling theropods as revealed by the dentary of the noasaurid Berthasaura leopoldinae (Cretaceous of Brazil)5
Developmental models shed light on the earliest dental tissues, using Astraspis as an example5
The utility of probability plotting in palaeobiology5
Planetary‐scale change to the biosphere signalled by global species translocations can be used to identify the Anthropocene5
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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
Finite element and microstructural analyses indicate that pteraspid heterostracan oral plate microstructure was adapted to a mechanical function5
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