• Bobrovskiy et al. (2020) and van Maldegem et al. (2020) argue that putative sponge
biomarkers can be generated from
algal sterols, and interpret their findings as undermining the interpretation of biomarkers found in Precambrian rocks posited as evidence of existence of animals before the latest Ediacaran. • Liu & Dunn (2020), describe filamentous organic structures preserved among
frond-dominated fossil assemblages from the
Ediacaran of
Newfoundland (
Canada), including filaments that appear to directly connect individual specimens of one
rangeomorph taxon, and interpret this finding as possible evidence that Ediacaran frondose taxa were
clonal. • A study on the age of the Ediacaran biota from the
Conception and
St. John's Groups at
Mistaken Point Ecological Reserve (Newfoundland, Canada) is published by Matthews et al. (2020). • Approximately 563-million-year-old Ediacaran biota is reported from the Itajaí Basin (
Brazil) by Becker-Kerber et al. (2020), representing the first record of Ediacaran macrofossils from
Gondwana in deposits of similar age to the
Avalon biota. • An Ediacaran
Lagerstätte with
phosphatized animal-like eggs, embryos,
acritarchs and
cyanobacteria is reported from the
Portfjeld Formation (
Peary Land,
Greenland) by Willman et al. (2020), representing the first record of a
Doushantuo type preservation of fossils (with diagenetic phosphate replacement of originally organic material) from
Laurentia reported so far. • A study on
biomarkers from Ediacaran sediments in the
White Sea area is published by Bobrovskiy et al. (2020), who interpret their findings as indicating that
eukaryotic algae were abundant among the food sources available for the
Ediacaran biota. • A study aiming to quantify changes of regional-scale diversity in marine fossils across time and space throughout the
Phanerozoic is published by Close et al. (2020). • A study on the structure of the Phanerozoic fossil record, aiming to determine relative impacts of extinctions and evolutionary radiations on the co-occurrence of species throughout the Phanerozoic, is published by Hoyal Cuthill, Guttenberg &
Budd (2020), who argue that their findings refute any direct causal relationship between the proportionally most comparable mass radiations and extinctions. • A study on the timing of known diversification and extinction events from
Cambrian to
Triassic, based on data from 11,000 marine fossil species, is published by Fan et al. (2020). • The discovery of a new, exceptionally-preserved Cambrian biota, with fossils belonging to multiple
phyla, is reported from the
Guzhangian Longha Formation (
Yunnan,
China) by Peng et al. (2020). • A study on changes in body size in skeletal animals from the Siberian Platform through the early Cambrian is published by Zhuravlev &
Wood (2020). • A study on the relationship between body size and extinction risk in the marine fossil record across the past 485 million years is published by Payne & Heim (2020). • A study on the diversification rates of Ordovician animals living on hard substrates, aiming to determine when they experienced their greatest origination rates, is published by Franeck & Liow (2020). • New information on the biotic composition of the
Silurian Waukesha Lagerstätte (
Wisconsin, United States) is presented by Wendruff et al. (2020), who report a biodiversity far richer than previously reported, and explore the
taphonomic history of the fossils of this biota. • A study on the diversity dynamics of the marine brachiopods, bivalves and gastropods throughout the
Late Palaeozoic Ice Age is published by Seuss, Roden & Kocsis (2020). • A study comparing the chemistry of fossil soft tissues of invertebrates and vertebrates from the
Carboniferous Mazon Creek fossil beds (
Illinois, United States) is published by McCoy et al. (2020), who report
Tullimonstrum gregarium as grouping with vertebrates in their analysis. • A study on the ages of known early–middle Permian
tetrapod-bearing geological formations, as indicated by Bayesian
tip dating methods, is published by Brocklehurst (2020), who interprets his findings as supporting the occurrence of the
Olson's Extinction. • A study on global
infaunal response to the Permian–Triassic extinction event, as indicated by data from trace fossils, is published by Luo et al. (2020). • A study on changes of marine
latitudinal diversity gradient caused by the Permian–Triassic mass extinction is published by Song et al. (2020). • A study on the latitudinal variation in Late Triassic tetrapod diversity, aiming to determine the relationship between latitudinal species richness and palaeoclimatic conditions, is published by Dunne et al. (2020). • Description of new fossil material of Late Triassic tetrapods from the Hoyada del Cerro Las Lajas site (
Ischigualasto Formation,
Argentina), and a study on the age of tetrapod fossils from this site (including fossils of
Pisanosaurus mertii) and their implications for the knowledge of the Late Triassic tetrapod evolution, is published by Desojo et al. (2020). • A review of the evidence of a major change in ecological community structure during the
Carnian, focusing on the temporal links of these biological changes with the
Carnian Pluvial Event and on the role of volcanic eruptions and associated
climate change as a possible trigger, is published by Dal Corso et al. (2020). • An assemblage of fossilized vomits and
coprolites is described from the Upper Triassic (Carnian) Reingraben Shales in Polzberg (
Austria) by Lukeneder et al. (2020), who evaluate the implications of these
bromalites for the knowledge of
pelagic invertebrates-vertebrates trophic chain of the Late Triassic Polzberg biota, and interpret their finding as evidence indicating that the
Mesozoic marine revolution has already started in the early Mesozoic. • A study on the dynamics of the Adamanian/Revueltian faunal turnover, based on fossil data from the
Petrified Forest National Park (
Arizona, United States), is published by Hayes et al. (2020). • A study on the
palynological record from the Carnian–Norian transition in the western
Barents Sea region is published by Klausen, Paterson &
Benton (2020), who interpret their findings as indicating that major sea-level changes across the vast delta plains situated in the northern
Pangaea might have triggered terrestrial turnovers during the Carnian–Norian transition and facilitated the gradual rise of the dinosaurs to ecosystem dominance. • Wignall & Atkinson (2020) argue that the
Triassic–Jurassic extinction event can be resolved into two distinct, short-lived extinction pulses separated by a several hundred-thousand-year interlude phase. • A study on changes in shell size of marine bivalves and brachiopods from the Iberian Basin (Spain) across the
Early Toarcian Oceanic Anoxic Event, aiming to determine the role of temperature for changes in body size of bivalves and brachiopods, is published by Piazza, Ullmann & Aberhan (2020). • A study on the impact of warming and disturbance of the carbon cycle during the Toarcian Oceanic Anoxic Event on marine benthic macroinvertebrate assemblages from the Iberian Basin is published by Piazza, Ullmann & Aberhan (2020). • A study on the persistence and abundance of an association of
serpulids and
hydroids during the Middle and Late Jurassic is published by Słowiński et al. (2020). •
Foster, Pagnac &
Hunt-Foster (2020) describe the
Late Jurassic biota from the Little Houston Quarry in the Black Hills of
Wyoming, including the vertebrate fauna which is the second-most diverse in the entire
Morrison Formation and the most diverse north of
Como Bluff. • A study on the age of the
Huajiying Formation (
China) and its implications for the knowledge of the timing of appearance and duration of the
Jehol Biota is published by Yang et al. (2020). • A study on the age of the biota from the Cretaceous
Burmese amber from Hkamti is published by Xing & Qiu (2020). • A study on extinction patterns of marine vertebrates during the last 20 million years of the Late Cretaceous, as indicated by fossils from northern
Gulf of Mexico, is published by Ikejiri, Lu & Zhang (2020), who report evidence of two separate extinction events: one in the
Campanian, and one at the end of the
Maastrichtian. • Rodríguez-Tovar et al. (2020) present evidence from trace fossils from the
Chicxulub crater indicating that full recovery of the
macrobenthic biota from this area was rapid, with the establishment of a well-developed tiered community within ~700 thousand years. • A study on the impact of the early
Cenozoic hyperthermal events on shallow marine
benthic communities, based on data from fossils from the
Gulf Coastal Plain, is published by Foster et al. (2020). • A study on the geology and fauna (including hominins) of the new Mille-Logya site (Afar,
Ethiopia) dated to between 2.914 and 2.443
Ma is published by
Zeresenay Alemseged et al. (2020), who evaluate the implications of this site for the knowledge of how hominins and other fauna responded to environmental changes during this period. • Studies on the magnitude and likely causes of
megafaunal extinctions in the
Indian subcontinent during the late Pleistocene and early Holocene are published by Jukar et al. (2020) and Turvey et al. (2020). • A new, diverse
megafauna assemblage that suffered extinction sometime after 40,100 (±1700) years ago is reported from the
South Walker Creek fossil deposits (
Queensland,
Australia) by
Hocknull et al. (2020), who evaluate the implications of this assemblage for prevailing megafauna extinction hypotheses for Sahul. • A study on ancient DNA of vertebrates and plants recovered from fossils and sediment from Hall's Cave (
Edwards Plateau,
Texas, United States), evaluating its implications for the knowledge of the climatic fluctuations from the Pleistocene to the Holocene on the local ecosystem, is published by Seersholm et al. (2020). • A study on the phylogenetic relationships of early amniotes, recovering
Parareptilia and
Varanopidae as nested within
Diapsida, will be published by Ford & Benson (2020), who name a new clade
Neoreptilia. • Regional-scale diversity patterns for terrestrial tetrapods throughout their entire
Phanerozoic evolutionary history are presented by Close et al. (2020), who attempt to determine how informative the fossil record is about true global paleodiversity. • A study on the impact of the appearance and evolution of herbivorous tetrapods on the evolution of land plants from the Carboniferous to the
Early Triassic is published by Brocklehurst, Kammerer & Benson (2020). • A study the terrestrial and marine fossil record of Late Permian to Late Triassic tetrapods, comparing species-level tetrapod biodiversity across latitudinal bins, is published by Allen et al. (2020). • In a study published by Chiarenza et al. (2020) the two main hypotheses for the mass extinction (the Deccan Traps and the Chicxulub impact) were evaluated using Earth System and Ecological modelling, confirming that the asteroid impact was the main driver of this extinction while the volcanism might have boosted the recovery instead. • Bishop, Cuff & Hutchinson (2020) outline a workflow for integrating paleontological data with biomechanical principles and modeling techniques in order to create musculoskeletal models and study locomotor biomechanics of extinct animals, using
Coelophysis as a case study. • Saitta et al. (2020) propose a framework for studying sexual dimorphism in non-avian dinosaurs and other extinct taxa, focusing on likely secondary sexual traits and testing against all alternate hypotheses for variation in the fossil record. • A study evaluating the utility of rare earth element profiles as proxies for biomolecular preservation in fossil bones, based on data from a specimen of
Edmontosaurus annectens from the Standing Rock Hadrosaur Site (
Hell Creek Formation;
South Dakota, United States), is published by Ullmann et al. (2020). • A study on the diversity and evolution of skull and jaw functions in sabre-toothed carnivores during the last 265 million years is published by Lautenschlager et al. (2020). ==Other research==