Lethaia

Papers
(The median citation count of Lethaia 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 2021-09-01 to 2025-09-01.)
ArticleCitations
Smithian and Spathian palaeontological records of the Vikinghøgda Formation in Central Spitsbergen65
Early ontogeny and other possible molluscan traits in hyolith biology and anatomy20
Mineralogy of Oligocene fossil wood, bone and associated sediments from the Petrified Forest protected area, New Cairo, Egypt18
Enhanced juvenile mortality of orbitolinids (larger benthic foraminifera) in the late early Aptian of the Langshan Formation, Tibet: a possible link to OAE1a?13
Soft tissue anatomy of pterosaur hands and feet – new information from Solnhofen region pterodactyloid specimens13
Discovery of plant cuticles in phyllite, late Pennsylvanian Southern Anthracite Field, eastern Pennsylvania, USA: a new research resource?13
Influence of substrate size and morphology on skeletobiont assemblages: a case study from the Middle Devonian brachiopods of Morocco12
Silicified pedunculate kutorginate brachiopods from the Cambrian (Stage 4) of Jordan11
Shell microstructures of latest Permian Rugosochonetidae (Brachiopoda): evidence from SEM‐ and CT‐scanned shell materials10
Ferruginous casts of bromalites in kaolin beds: microbial ferrihydrite‐goethite transformation as early stage taphonomy in lacustrine and riparian sediments10
Linear morphometry and shell growth of the bivalve Tagelus plebeius as an indicator for salinity in Holocene South American estuaries9
The fossil record of lepidopteran caterpillars in Dominican and Mexican amber9
Palaeoenvironmental study of benthic foraminifera from the late Pleistocene Puente de Pascua Formation type locality, Buenos Aires province, Argentina9
New taphonomic and sedimentological insights into the preservation of high-relief Ediacaran fossils at Upper Island Cove, Newfoundland8
Revisiting the aerobic capacity of Notosuchia (Crocodyliformes, Mesoeucrocodylia)8
Articulated and dislocated infaunal echinoids as unique markers of hypoxic environments from the Miocene of Central Paratethys7
Eurypterid morphology and implications for ecdysis and evolutionary longevity7
Interspecies and intraspecific variability in the trilobites Duyunaspis and Balangia from the Cambrian Series 2 (Stage 4) of Jianhe, South7
Early-Middle Miocene coralline algal assemblages from the Siirt province, southeastern Türkiye: microtaphofacies analysis and palaeoenvironmental implications6
Is there any evidence for the presence of extensive fibrolamellar complex in Notosuchia? New data on Araripesuchus wegeneri6
Identification of conodont fossils in pelagic deep‐sea siliceous sedimentary rocks using laboratory‐based X‐ray computed microtomography6
Fossil fish provide evidence of geomelanin preservation with implications on the visual accuracy of an extinct fish species6
Southernmost record of the pachycephalosaurine Stygimoloch spinifer and palaeobiogeography of latest Cretaceous North American dinosaurs5
Environmental interpretation of giant trace fossils from the lower Kimmeridgian (Upper Jurassic) of the Iberian Chain (Spain) from lithofacies, microfossil and ichnofossil assemblages5
Nautilid beaks: unsuspected disparity and palaeoecological interpretation5
Taphonomic and reworking processes isolating cephalopod septa and chamber fillings5
Palaeoenvironmental analysis of bivalve-dominated concentrations from the lower‒middle Miocene succession, Gebel Gharra, Cairo-Suez District, Egypt5
Newly discovered Wuchiapingian to Olenekian conodonts from the Longgar area, southern Lhasa Terrane and their palaeobiogeographical implications5
Late Quaternary terrigenous plant and coaly fragments found at the Vestnesa Ridge, Fram Strait: implications for postglacial plant colonization at Svalbard5
Cirrus versus radice: a brief study of confused crinoid terminology5
Bioerosion, encrustation, and taphonomic pathways of Nummulites tests and the palaeoenvironmental implications: Oligocene interval of the Kutch Basin, India4
A demineralized osteostracan fossil from the Silurian Kalana Lagerstätte of Estonia: revealing its internal anatomy and uncovering a unique type of fossilization4
Nothosaur tracks from the Middle Triassic of Spain suggest a global distribution for distinctive swim track assemblages4
The Skyberg Lagerstätte from the Mjøsa area, Norway: a rare window into the late early Cambrian biodiversityof Scandinavia4
Upper Viséan foraminiferal and algal diversity at Benburb, Northern Ireland as a tool of high-resolution biostratigraphy, and correlation of Late Viséan-Early Serpukhovian successions in Ireland and B4
Early Cretaceous pterosaur guano deposit from central Oregon, USA4
Thalassinoides and Olenichnus in the Terreneuvian carbonates of the Igarka Uplift, NW Siberian Platform4
Palaeotectonic reconstructions of the Central Asian folded belt in the Silurian Tuvaella and Retziella brachiopod fauna locations4
Comparison of sclerobiont communities between three brachiopod host species from the Upper Ordovician Fairview Formation, Eastern USA4
Quaternary environmental evolution of the Argentinean Pampa Deprimida based on mollusc and ostracod analysis4
Neoichnology of the burrowing mayfly Tortopus circumfluus and its bearing on the ichnofossil Glossifungites gingrasi4
Palaeoenvironmental study of two new foraminifera sites from Late Pleistocene transgressive deposits, northeast Buenos Aires Province, Argentina4
The largest complex burrow system from the early Cambrian of Sweden, probably made by priapulids in response to tidal currents3
Morphology and mode of life of a peculiar Devonian microconchid tubeworm Aculeiconchus from Wyoming, USA3
Lethaia Editorial Briefing3
Early Palaeozoic Discinocarina: a key to the appearance of cephalopod jaws3
Dental histology and attachment tissues in Notosuchus terrestris (Crocodyliformes, Notosuchia): palaeobiological implications3
Names for trace fossils 2.0: theory and practice in ichnotaxonomy3
Arguments for interpreting the vertebrate functional neck as an exaptation for terrestriality3
The influence of volcanic activity and trophic state on plant taphonomic processes in Triassic lacustrine-deltaic systems of western Gondwana3
Scale dependent diversity of bryozoan assemblages in the reefs of the Late Ordovician Vasalemma Formation, Estonia3
Integrated stratigraphical study of the Rhuddanian-Aeronian (Llandovery, Silurian) boundary succession in the Rheidol Gorge, Wales: a proposed Global Stratotype Section and Point for the base of the A3
A microfossil evidence for the composition of fish communities in the Late Triassic of Tethys: examples from Cassian Formation, Italy3
Biofilm harvesters in coastal settings of the early Palaeozoic3
Spatiotemporal dynamics of nektonic biodiversity and vegetation shifts during the Smithian–Spathian transition: conodont and palynomorph insights from Svalbard3
Development and trunk segmentation of a redlichiid trilobite from Cambrian Series 2 of China3
Recurring taphonomic processes in the carnivoran‐dominated Late Miocene assemblages of Batallones‐3, Madrid Basin, Spain3
First fossil evidence of leaf‐feeding caterpillars from India and their feeding strategies3
Lower and upper jaws of the Early Permian goniatitid ammonoids3
Early Jurassic coral reef development outside Tethys: an example from western Argentina3
High‐resolution Pliocene–Pleistocene calcareous nannofossil distribution and palaeoenvironmental changes in the northwest Nile Delta, Egypt3
Could the asymmetrical commissure in rhynchonellide brachiopods be an adaptive trait?2
Ecomorphological datasets: comment on Hopkins (2022)2
Biomineralization of primary carbonate cements: a new biosignature in the fossil record from the Anisian of Southern Italy2
Bayesian analysis of ultra-high-resolution ostracod record reveals the tempo and structure of the late Wenlock Mulde Event2
Morphological and compositional analyses of coprolites from the Upper Cretaceous Bauru Group reveal dietary habits of notosuchian fauna2
Biomarker analysis of invertebrate fossils preserved in concretions from the Lower Cretaceous Allaru Mudstone of Queensland, Australia2
Taphonomy and its significant role in palaeoenvironmental reconstruction of the upper Turonian actaeonellid gastropod concentrations of Abu Roash, Western Desert, Egypt2
Predator–prey interactions among Pliocene molluscs from the Tjörnes Peninsula, Iceland; across the trans‐Arctic invasion2
Planktonic foraminifera assemblages from the Brazil–Malvinas Confluence: palaeoceanographic implications of sub-surface temperature reconstructions in the western South Atlantic2
Response of Bathonian–Oxfordian transgressive-regressive cycles on foraminiferal morphogroups, and diversity: a case study from shallow marine deposits in north Gulf of Suez, Egypt2
Late Devonian fossils of New South Wales and early tetrapod habitats2
Upper Cretaceous foreland flysch deposits from the Neotethyan Intra-Pontide Ocean: geological and palaeontological evidence from the Elmadağ Olistostrome of Ankara, central Türkiye2
The concept of ‘heteromorph ammonoids’2
Oichnus Bromley as evidence of predator presence in the Canadian High Arctic2
Guilds of large carnivorans during the Pleistocene of Europe: a community structure analysis based on foraging strategies2
The mobile domicile boring Trypanites mobilis revisited – new observations and implications for ecosystem recovery following the Cretaceous – Palaeogene mass extinction1
Integrated calcareous nannofossil and stable isotope stratigraphy across the Danian-Selandian boundary, west central Sinai, Egypt1
Biostratigraphical significance of a new trilobite fauna from the Harkless Formation (upper Stage 4, Series 2, Cambrian), Nevada, USA1
Palaeoecology of the Southern chamois from Valdegoba Cave (Burgos, Spain) and its exploitation by the Neanderthals1
Naticid gastropod predation on bivalve assemblages across the K-Pg mass extinction boundary in Rajahmundry, India1
Fate of calcareous nannofossils during the Rhaetian (Late Triassic): evidence from the Northern Calcareous Alps, Austria1
The earliest calcified cyanobacteria from the Cambrian Terreneuvian at the western margin of the Yangtze Plate, China1
Conservative ontogenetic trajectories of septal spacing during the post-embryonic stage in Cretaceous ammonoids of the subfamily Desmoceratinae1
Sclerobionts associated with Orbiramus from the Early Ordovician of Hubei, China, the oldest known trepostome bryozoan1
Barnacle taphonomy and ultrastructure: comparing modern and fossil shells from the western Mediterranean1
First record of the ichnospecies Oichnus ovalis in a Jurassic ammonite1
Bioerosion and palaeoecological association of osteophagous insects in the Maastrichtian dinosaur Arenysaurus ardevoli1
Diversity, palaeoecology and palaeoenvironmental significance of the Eocene chondrichthyan assemblages of the Bolca Lagerstätte, Italy1
Foraging flatworms and roundworms caught in the act: examples from a Middle Triassic mud flat in Germany1
Bone microstructure in terrestrial Mesozoic Crocodylomorpha: Neuquensuchus and notosuchians1
Issue Information1
Ecophenotypic variation in the rudist bivalve Polyconites hadriani on an Aptian platform-slope facies gradient from the western Maestrat Basin, eastern Iberia1
Mandibular force profiles of Alioramini (Theropoda: Tyrannosauridae) with implications for palaeoecology of this unique lineage of tyrannosaurid dinosaurs1
The evolution of thecideide microstructures and textures: traced from Triassic to Holocene1
Presumed chaetetids in Smithian (early Olenekian, Early Triassic) microbial-sponge limestones, Rock Canyon, Arizona, USA1
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