July 2024
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95 Reads
Journal of Systematic Palaeontology
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July 2024
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95 Reads
Journal of Systematic Palaeontology
May 2024
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75 Reads
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2 Citations
Proceedings of the Geologists Association
February 2024
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169 Reads
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4 Citations
Geological Society London Special Publications
Pterosaurs, the first vertebrates to evolve powered flight, dominated Mesozoic skies from the Late Triassic to the end Cretaceous, a span of around 154 million years (∼220 mya to 66 mya). They achieved their greatest diversity in the mid-Cretaceous and had become globally distributed, even occurring at high latitudes and in a wide range of habitats. The pterosaur record is dominated by occurrences in conservation Lagerstätten in just a handful of countries and a narrow range of temporal windows, most notably China, Germany and Brazil and the Middle-Upper Jurassic and mid-Cretaceous respectively. During the Cretaceous two major pterosaur clades evolved edentulism, such that by the end of the Cretaceous, no toothed pterosaurs survived, having become extinct by the mid-Cenomanian. A distinctive aspect of pterosaur evolution during the mid-Cretaceous was the achievement of gigantic wingspans, perhaps in excess of 10 metres, hyper-elongation of the neck vertebrae in Azhdarchidae, and the evolution of highly elaborate cranial crests. For many years, pterosaur diversity in the terminal stage of the Late Cretaceous was regarded as low, but discoveries in the last few decades have indicated pterosaur taxic diversity remained high until the end Maastrichtian, although morphological diversity may have been low. The demise of the Pterosauria at the K/Pg boundary was most likely due to the same causes as the coeval dinosaur extinction associated with the Chicxulub bolide impact and its environmental repercussions. Faunal replacement by avians is no longer considered a significant factor in pterosaur extinction.
September 2023
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75 Reads
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3 Citations
Cretaceous Research
August 2023
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120 Reads
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6 Citations
Evolving Earth
July 2023
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309 Reads
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1 Citation
Cretaceous Research
Ganoine-scaled fishes belonging to the superfamily Lepisosteoidea, more commonly known as gars, are an ancient lineage with origins in the Mesozoic, first appearing in the Kimmeridgian, Late Jurassic. The Mesozoic gar fossil record is patchy, mostly consisting of disarticulated remains, with only a few partially or mostly complete specimens being extremely rare. Extant gars typically occur in freshwater and brackish environments, with rare observations of a few species frequenting saline waters although little is known of their marine ancestors. Here we describe a new genus and species, Grandemarinus gherisensis gen. et sp. nov., an unusually short-snouted gar from the Upper Cretaceous (Turonian) Akrabou Formation of Morocco. The short-snouted cranial bauplan is superficially convergent with the Eocene freshwater genera Cuneatus and Masillosteus, although a phylogenetic analysis resolves the new gar as the sister taxon to the Lepisosteini (Oniichthys, Lepisosteus, Atractosteus), falling outside of Masillosteinae (Masillosteus, Cuneatus). Gars likely originated as fully marine fishes during the Late Jurassic, and during Early Cretaceous times successfully invaded freshwater ecosystems. The new gar described here is likely a late surviving member of this early marine lineage. The new lepisosteiform is the first complete gar described from a Cretaceous marine deposit; representing a vital clue to help decipher the early evolution and ecology of Lepisosteidae. The taphonomy of the specimen is discussed within the context of a fully marine carbonate Konservat Lagerstätte.
May 2023
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82 Reads
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4 Citations
Cretaceous Research
The oldest record of a dortokid turtle (Testudines, Pan-Pleurodira) and the first occurrence of the group in the UK is reported. This find corresponds to the oldest pan-pleurodiran turtle in the country, and the only one from the Mesozoic of the UK. The new specimen, from the Lower Cretaceous (Barremian) Wessex Formation of the Isle of Wight, comprises a relatively complete shell with post cranial elements within a calcite-filled shell vacuity. Micro CT scanning has revealed these tiny bones to include cervical, dorsal and caudal vertebrae, scapulae, pelvic girdle and appendicular elements. In addition, aspects of the internal morphology of the carapace and plastron are revealed. No features allow the new specimen to be distinguished from the coeval Eodortoka morellana of Spain, and we therefore identify it as Eodortoka cf. morellana.
May 2023
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140 Reads
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3 Citations
Proceedings of the Geologists Association
Four isolated cervical vertebrae from the Kimmeridge Clay Formation (Upper Jurassic, Kimmeridgian) of Abingdon, Oxfordshire, England are identified as from a pliosaurid plesiosaurian sauropterygian on account of their shortness relative to width and height, their near platycoelous nature and the location of tall rib facets on the centrum body. They are noteworthy for their size, with a maximum width of 269 mm, maximum height of 222 mm and maximum length of 103 mm. Simple scaling and comparisons with cervical vertebrae of Mid Jurassic pliosaurs Peloneustes and Liopleurodon, and the Early Cretaceous Stenorhynchosaurus and Sachiasaurus suggest a total body length of between ~9.8 m and 14.4 m for the Abingdon Kimmeridge Clay pliosaur. Likely the true length was towards the higher end of this range. A genus and species cannot be confidently determined on the basis of the described material, but they likely belong to Pliosaurus sp. or a similar animal, for which a precise neck length is not known. We estimate a neck length of 0.77 m for Pliosaurus ?brachyspondylus based on the average cervical lengths provided for specimen CAMSM J.35991.
March 2023
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54 Reads
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3 Citations
Cretaceous Research
February 2023
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142 Reads
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1 Citation
Cretaceous Research
... Linear regression performed on a bivariate plot of wingspan versus ulna length for the entire dataset was used to predict the wingspan of OAKRM 2023.66 using the predicted minimum length when complete of~300 mm and wingspan calculated at 2.1 times the forelimb length. This method follows that of Etienne et al. (2024). ...
May 2024
Proceedings of the Geologists Association
... Many fossil Konservat Lagerstätten have become well-known for the quality of preservation, and to some degree abundance of pterosaur skeletons (Unwin, 2005;Wellnhofer, 1991;Witton 2013). Perhaps most notable among these are the Upper Jurassic Solnhofen-type plattenkalk formations of southern Germany (e.g., Tischlinger & Frey 2015), the Lower Cretaceous Crato and Santana formations of Brazil (e.g., Martill & Brito, 2017) and the Yixian and Jiufotang formations of China (e.g., Lü et al., 2013). In all of these deposits, pterosaurs occur as partial or fully articulated skeletons, sometimes in 3D, and often with associated soft tissues preserved (Bestwick, 2018;Frey et al., 2003;Kellner et al., 2010;Martill & Unwin, 1989). ...
January 2018
... These fossils have greatly expanded the diversity, disparity, and temporal distribution of Mesozoic birds, refining our knowledge of the evolutionary path leading to the characteristic avian body plan, such as feathers and powered flight, locomotion and habitat differentiation, diet and digestion, reproduction and development, feather colours and display. In particular, studies on the geological background of the Jehol Biota that produced the majority of the Chinese Cretaceous birds have provided important clues to our understanding of the taphonomy as well as the interaction between deep geology process and biological evolution in the Early Cretaceous. the first vertebrates to evolve powered flight, dominated Mesozoic skies from the Late Triassic to the end-Cretaceous, a span of around 154 million years(Martill and Smith 2024). They achieved their greatest diversity in the mid-Cretaceous and had become globally distributed, even occurring at high latitudes and in a wide range of habitats. ...
Reference:
The Cretaceous World (GSL SP544)
February 2024
Geological Society London Special Publications
... Ornithopods are the most common dinosaurs registered in the Lower Cretaceous sediments of Europe. This group is represented by small hypsilophodontids, such as Hypsilophodon foxii (e.g., [1,2]), Gideonmantellia [3], and Vectidromeus [4]; scarce rhabdodontomorphans [5]; small dryosaurids like Valdosaurus [6]; and medium to large styracosternans (e.g., [7][8][9][10][11][12][13][14][15][16][17][18][19][20][21][22][23]). The latter is the most prominent and well-known group in Europe, especially in the pre-Albian sediments, with an exquisite representation constituted by the mediumsized Mantellisaurus [8,24], Morelladon [16], Brighstoneus [22], and Portellsaurus [23] and the large-sized taxa Magnamanus [25], Iguanodon galvensis [18,26], and I. bernissartensis [7,15,17]. ...
September 2023
Cretaceous Research
... The nomenclature Morocco (south-eastern) and Algeria (western) showing the outcrops of the Kem Kem Group in the Tafilalt region. The Kem Kem Group rock exposures were adapted from Sereno et al. (1996) by Smith et al. (2023b) and modified here. The star indicates Taouz, the area from which the fossils described here come from. ...
August 2023
Evolving Earth
... Current lepisosteids are mostly freshwater, occasionally frequenting brackish waters; while only one species, Atractosteus tristoechus, survives marine environments Grande, 2010). However, during the Mesozoic, there were more taxa that were considered fully marine (Alvarado-Ortega et al., 2016;Brito et al., 2017;Cooper et al., 2023). ...
July 2023
Cretaceous Research
... This sandstone occurs just above the Hauterivian/Barremian boundary ( [27]; see also [28]), and we therefore regard its stratigraphic age as early Barremian. ...
May 2023
Cretaceous Research
... The predatory plesiosaur clade Rhomaleosauridae that dominated in Early Jurassic seas started to disappear, meeting its final demise in the Callovian (late Middle Jurassic; ∼161.5 Ma) (e.g., Benson et al., 2015b), while Pliosauridae and Plesiosauroidea diversified. Pliosaurids established a successful clade of macropredators (Thalassophonea) that had regulated the upper tier of marine ecosystems since at least the early Bajocian (∼171 Ma) (Sachs et al., 2023) until the Turonian (early Late Cretaceous; ∼90 Ma; Madzia, 2016;Madzia et al., 2019) and comprised some of the largest aquatic predatory tetrapods that have ever lived, with forms exceeding lengths of 10 m (Knutsen et al., 2012b;Benson et al., 2013;Martill et al., 2023). Plesiosauroids, in turn, switched from microcleidid-rich communities common for Toarcian European epeiric seas to cryptoclidid faunas that represented the globally dominant plesiosauroid components in the Middle and Late Jurassic until they were replaced by leptocleidians and elasmosaurids near the Jurassic-Cretaceous transition (Benson and Druckenmiller, 2014). ...
May 2023
Proceedings of the Geologists Association
... A recent alternative rank-free phylogeny for Actinopterygii proposes Acipenseroidei as a synonym of Acipenseriformes but with the exclusion of Chondrosteidae and Peipiaosteidae as "pan-acipenseriforms" (Near & Thacker, 2024). Both fossil and living acipenseriforms are endemic to the northern hemisphere (but see Martill [2023] for a possible acipenseroid from the Upper Cretaceous of Gondwana) and have anatomically specialized skeletons with highly reduced bone ossification (Bemis et al., 1997;. Being predominantly cartilaginous, their unfavorable skeletal mineralogy is undoubtedly a key bias for their perceived scarcity in the fossil record as fragmentary remains are often difficult to identify at the genus or even family level (e.g., Hilton & Grande, 2006;Hilton et al., 2021). ...
March 2023
Cretaceous Research
... There are also abundant teeth, scales, and other remains of sauropods, pterosaurs, crocodyliforms, and chondrichthyan fishes (e.g., Amiot et al., 2004;Beevor et al., 2021;Cavin et al., 2010;Dutheil, 1999;Holwerda, 2020;Holwerda et al., 2018;Ibrahim et al., 2020a;Ibrahim et al., 2014a;Läng et al., 2013;McGowan & Dyke, 2009;Richter et al., 2013;Russell, 1996;Sereno et al., 1996;Smyth et al., 2020a;Wilson & Allain, 2015). Theropod (dental and non-dental) remains from the Kem Kem Group have previously been ascribed to Abelisauridae (Chiarenza & Cau, 2016;D'Orazi Porchetti et al., 2011;Mahler, 2005;Russell, 1996;Smyth et al., 2020a;Zitouni et al., 2019), Noasauridae (Evans et al., 2015;Smyth et al., 2020a), Spinosauridae (e.g., Dal Sasso et al., 2005;Evers et al., 2015;Hendrickx et al., 2016;Ibrahim et al., 2020b;Ibrahim et al., 2014bIbrahim et al., , 2020aMilner, 2003;Smith & Martill, 2023;Smyth et al., 2020b), Carcharodontosauridae Cau et al., 2012Cau et al., , 2013Ibrahim et al., 2020a;Paterna & Cau, 2022;Sereno et al., 1996), Dromaeosauridae (Amiot et al., 2004;Ibrahim et al., 2020a;Richter et al., 2013) as well as the indeterminate averostran Deltadromeus Rauhut & Carrano, 2016;Sereno et al., 1996), revealing a particularly high theropod diversity in the middle Cretaceous of northern Africa (Benyoucef et al., 2015;Fanti et al., 2014;Ibrahim et al., 2020a;Läng et al., 2013). Historically, isolated theropod teeth from the Kem Kem Group of Morocco were first reported and illustrated in the mid 20th century by French paleontologist René Lavocat (1948) and French geologists Georges Choubert and colleagues (1952), respectively (Cavin et al., 2010). ...
February 2023
Cretaceous Research