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Plesiosaur

Plesiosauria is an extinct clade of secondarily aquatic marine reptiles within the larger group Sauropterygia, characterized by a unique body plan consisting of four large, paddle-like flippers used for propulsion and, in many species, an elongated neck supporting a small head.^[1] These reptiles inhabited the world's oceans from the Late Triassic to the end of the Late Cretaceous, spanning approximately 135 million years and coexisting with other marine fauna such as ichthyosaurs and ammonites.^[2] Fossils of plesiosaurs have been discovered on every continent, indicating a global distribution and high diversity, with over 100 recognized genera.^[3] Plesiosaurs exhibited two primary morphotypes that defined their ecological roles: plesiosauromorphs, which had long necks (sometimes comprising half their body length) and small heads suited for foraging in open water or near the surface, and pliosauromorphs, featuring short necks, massive skulls, and powerful jaws adapted for predatory lifestyles targeting large prey like fish, squid, and other marine reptiles.^[4] Body sizes varied widely, from small species around 3 meters in length to giants reaching up to 15 meters, such as the Late Jurassic Pliosaurus or the Late Cretaceous Elasmosaurus.^[5] Their limb proportions also differed between morphotypes, with plesiosauromorphs typically having longer forelimbs than hindlimbs for enhanced maneuverability, while pliosauromorphs showed the opposite for powerful thrusting.^[4] The evolutionary history of Plesiosauria reflects adaptations to Mesozoic marine environments, including responses to oceanic anoxic events and continental drift during the breakup of Pangaea, which influenced their diversification particularly in the Jurassic and Cretaceous periods. Recent discoveries, such as the 2025 description of Plesionectes longicollum from Early Jurassic deposits in Germany, continue to refine understanding of early diversification during such events.^[2]^[6] Notable early forms appeared at the Triassic-Jurassic boundary, such as Atychodracon megacephalus, while the group reached peak diversity in the Late Jurassic before a decline leading to their extinction.^[7] Plesiosaurs went extinct during the Cretaceous-Paleogene (K/Pg) mass extinction event approximately 66 million years ago, alongside non-avian dinosaurs and many other marine groups, likely due to a combination of asteroid impact, volcanism, and environmental upheaval.^[8] Their fossil record, ranging from complete skeletons to fragmentary remains, continues to provide insights into ancient marine ecosystems and locomotor evolution.^[9]

History of discovery

Early European finds

The discovery of the first nearly complete plesiosaur skeleton occurred on December 10, 1823, when Mary Anning unearthed Plesiosaurus dolichodeirus from the Blue Lias Formation along the cliffs at Lyme Regis, Dorset, England.^[10] This specimen, measuring about nine feet in length, was embedded in the Lower Jurassic limestones and shales characteristic of the Jurassic Coast, a region renowned for its fossil-rich marine deposits from approximately 200 million years ago.^[11] Excavating the fossil presented significant challenges, as Anning worked single-handedly on the steep, unstable cliffs prone to frequent landslides and erosion, often in perilous winter conditions that heightened the risk of injury or burial under falling rock.^[12] The find sparked immediate interest among geologists but also drew skepticism; French anatomist Georges Cuvier, upon reviewing sketches, initially dismissed it as a forgery, suspecting it was a composite assembled from parts of an ichthyosaur and a crocodile.^[10] Such misinterpretations reflected early uncertainties, with some comparing the creature's form to elongated fish or crocodiles rather than recognizing it as an extinct reptile.^[13] Anning's careful preparation and documentation helped counter these doubts, leading to its formal validation by William Daniel Conybeare, who confirmed the specimen's authenticity and described it in a presentation to the Geological Society of London on February 10, 1824.^[11] In the ensuing years of the early 1820s, additional plesiosaur specimens emerged from similar Jurassic strata in Dorset, including fragmentary remains that bolstered the emerging understanding of these long-necked marine reptiles as a distinct group separate from ichthyosaurs.^[14] Comparable finds in Yorkshire, such as partial skeletons from the Upper Lias beds near Whitby reported around 1824, further contributed to this recognition by providing comparative material from northern European sites.^[15] These early European discoveries, concentrated in England's coastal exposures, ignited widespread fascination with marine reptiles and laid the groundwork for plesiosaur studies amid the burgeoning field of paleontology.^[13]

Initial naming and classification

The genus Plesiosaurus was first proposed in 1821 by geologists Henry De la Beche and William Daniel Conybeare in a paper presented to the Geological Society of London, based on fragmentary remains from Lyme Regis that suggested a novel marine reptile intermediate between known forms like Ichthyosaurus and crocodilians. The name derives from the Greek plēsios, meaning "near" or "close to," and sauros, meaning "lizard," reflecting its perceived affinities to both reptilian and piscine traits.^[16] In 1824, Conybeare formally described the type species Plesiosaurus dolichodeirus using a nearly complete skeleton discovered by Mary Anning at Lyme Regis, providing the first detailed anatomical illustration and affirming the genus's validity.^[17] The species epithet dolichodeirus combines Greek dolikhos ("long") and deirē ("neck"), highlighting the specimen's distinctive elongated cervical region.^[18] Initial reception of Plesiosaurus involved significant debate regarding its authenticity, particularly in the 1820s, as the creature's unusual morphology—combining a small head, long neck, broad body, and four flippers—challenged contemporary understandings of vertebrate anatomy. Prominent French naturalist Georges Cuvier expressed skepticism upon reviewing sketches sent by Conybeare, suspecting the specimen might be a hoax assembled from disparate parts, such as a crocodile head grafted onto a fish-like body.^[13] De la Beche and Conybeare addressed these concerns in their Geological Society publications, emphasizing the fossil's integrity through meticulous descriptions and comparisons to established marine reptiles, ultimately convincing Cuvier of its genuineness by April 1824 after he examined detailed drawings.^[14] Early taxonomic placement positioned Plesiosaurus as a distinct group of marine reptiles, closely allied with but separate from Ichthyosaurus, due to differences in skeletal structure such as the expanded ribs forming a barrel-shaped torso and the absence of a dorsal fin. Conybeare's 1824 analysis further delineated it from other saurians, noting its unique paddle-like limbs and neck vertebrae, which foreshadowed its later inclusion within the clade Sauropterygia alongside nothosaurs and other long-bodied aquatic reptiles.^[17] By the 1830s, these distinctions solidified Plesiosaurus as a foundational taxon for understanding Mesozoic marine reptile diversity, independent of more streamlined forms like ichthyosaurs. A key integration of Plesiosaurus into broader scientific discourse appeared in William Buckland's 1835 Bridgewater Treatise on geology and mineralogy, where he discussed the fossil as evidence of divine design in creation, portraying its adaptations—such as the flexible neck for foraging and robust flippers for propulsion—as harmonious examples of purposeful anatomy within a pre-flood world. Buckland's treatment reconciled emerging paleontological evidence with natural theology, emphasizing how Plesiosaurus exemplified the power, wisdom, and goodness of God manifest in extinct species.

North American and global discoveries

The expansion of plesiosaur discoveries beyond Europe began in the mid-19th century with significant finds in North America, particularly along the Western Interior Seaway, a vast Cretaceous inland sea that bisected the continent. In Kansas, early explorations in the 1860s yielded some of the first substantial plesiosaur specimens from the region, including elasmosaurids from the Smoky Hill Chalk and Pierre Shale formations. Physician Theophilus H. Turner discovered a nearly complete Elasmosaurus platyurus skeleton near Fort Wallace in 1867, which was shipped to paleontologist Edward Drinker Cope for study; Cope named the species in 1868, noting its extraordinary 72 cervical vertebrae that highlighted the group's long-necked diversity.^[19]^[20] These finds built on earlier fragmentary remains from the 1840s in the same formations, though not formally identified until later, and demonstrated plesiosaurs' abundance in shallow marine environments.^[19] Cope's work intensified during the 1860s and 1870s amid the "Bone Wars," his rivalry with Othniel Charles Marsh, which spurred rapid collection across the American West. Cope described numerous plesiosaur taxa from Kansas and surrounding states, including Polycotylus latipinnis in 1869 based on a skull and cervical vertebrae from the Niobrara Chalk, and other elasmosaurids like Cimoliasaurus maccoyi from the same deposits. These specimens, often excavated from eroding riverbanks and chalk beds, revealed short-necked polycotylids alongside long-necked forms, expanding understanding of plesiosaur morphological variation and their role as top predators in the seaway. Cope's contributions, detailed in his 1870 monograph on North American plesiosaurs, documented over a dozen species, though some later required revision due to hasty descriptions amid the competition.^[21]^[22] Global exploration in the 20th century further broadened the record, with major Australian discoveries in the 1920s showcasing large pliosaurids from Queensland's Cretaceous rocks. Heber A. Longman described Kronosaurus queenslandicus in 1924 from a partial skull and vertebrae collected near Hughenden, emphasizing its massive 2.5-meter-long cranium with robust teeth suited for crushing prey; earlier fragments from 1899 had hinted at such giants, but this specimen confirmed the presence of apex predators in Austral Gondwanan seas. The find, from the Toolebuc Formation, underscored plesiosaurs' southern distribution and prompted expeditions that recovered additional material, including a near-complete skeleton in the 1930s.^[23]^[24] In the Southern Hemisphere, 20th-century finds in Antarctica, South America, and New Zealand revealed late-surviving Gondwanan faunas. In Argentina, Angel Cabrera named Aristonectes parvidens in 1941 from a skull and partial skeleton discovered in 1940 near Comodoro Rivadavia in Chubut Province's Maastrichtian strata, marking one of the first well-documented elasmosaurids from high southern latitudes with its specialized filter-feeding adaptations. Antarctic expeditions in the 1980s and 1990s uncovered plesiosaur remains from the James Ross Basin, including elasmosaurid vertebrae and limbs from Seymour Island's Lopez de Bertodano Formation in 1989, indicating diverse late Cretaceous assemblages in polar waters. In New Zealand, the cryptoclidid Kaiwhekea katiki was collected from Shag Point in the 1980s and formally described in 2002 by Arthur Cruickshank and Ewan Fordyce; this nearly complete specimen from the Maastrichtian Katiki Formation, with its 6-meter length and associated skull elements, evidenced an austral radiation of plesiosaurs distinct from northern forms. These discoveries collectively illustrated plesiosaurs' worldwide proliferation and adaptation across Mesozoic oceans.^[25]^[26]

Recent paleontological advances

In the 2010s and 2020s, computed tomography (CT) scanning and 3D modeling have revolutionized the study of plesiosaur specimens by enabling non-destructive analysis of internal structures and reconstructions of locomotion. For instance, a 2021 CT scan of elasmosaurid plesiosaur skulls from the Late Cretaceous revealed minimal evolutionary changes in cranial architecture over millions of years, suggesting stable adaptations to aquatic predation.^[27] Similarly, CT imaging of a 19th-century New Zealand specimen of Tuarangisaurus keyesi in 2022 demonstrated that these plesiosaurs likely swam with their heads directed downward, challenging prior assumptions about neck posture in long-necked forms.^[28] More recently, in 2024, CT scans of a juvenile plesiosaur from Queensland, Australia, uncovered details of its incomplete skeleton, including vertebral counts that informed growth patterns in early ontogeny.^[29] Recent years have seen the description of several new plesiosaur species, enhancing understanding of their diversity and early evolution. In 2024, exceptionally preserved skeletons from the Lower Jurassic of Germany led to the identification of a transitional plesiosauroid, bridging gaps between basal and derived forms and indicating rapid diversification in the group's post-Triassic radiation.^[30] This was followed in 2025 by Plesionectes longicollum, an early-diverging plesiosauroid from the Posidonia Shale of Germany, based on a nearly complete skeleton that measured about 3.2 meters and featured a proportionally long neck for its era.^[6] Also in 2025, Traskasaura sandrae, a 12-meter-long elasmosaurid from Late Cretaceous deposits in British Columbia, Canada, was named from a partial skeleton, highlighting regional endemism in high-latitude marine reptiles with robust teeth suited for crushing prey.^[31] Additionally, new material of Kimmerosaurus langhami from the Kimmeridge Clay Formation in Dorset, UK, described in 2025, provided insights into cryptoclidid anatomy, including enhanced data on neck flexibility through comparative 3D reconstructions.^[32] Isotopic analyses from 2023 to 2025 have begun to elucidate plesiosaur migration and thermoregulation, drawing on oxygen and other stable isotopes from fossils across Europe and North America. A 2024 study of southern sauropterygians, including early plesiosauromorphs, used isotopic paleotemperatures to show that high-latitude barriers did not significantly impede marine reptile migrations during the Triassic-Jurassic transition.^[33] In 2025, oxygen isotope analysis of 247 bones and teeth from various Mesozoic marine reptiles, encompassing plesiosaurs, reassessed body temperatures and supported ectothermic strategies in many taxa, with values indicating habitat temperatures of 15–25°C and limited evidence for long-distance migrations in short-necked forms.^[34] Advances in exceptional preservation have revealed soft tissues and dietary evidence, filling gaps in plesiosaur paleobiology. A 2025 analysis of a 183-million-year-old Plesiopterys wildi specimen from Germany's Posidonia Shale, using microscopy on preserved skin, documented a mosaic of smooth integument on the body and small scales on the tail and flippers, akin to modern sea turtles.^[35] In Australia, the 2023 reexamination of "Eric," a Umoonasaurus demoscyllus specimen from the Early Cretaceous, identified gastroliths in the stomach region via 3D modeling, confirming a diet of shelled prey and providing the first direct evidence of gastrolith use in Australian plesiosaurs.^[36] These finds underscore the role of Lagerstätten in preserving delicate features previously inaccessible through traditional methods.

Classification and evolution

Phylogenetic relationships

Plesiosauria represents a monophyletic clade within the broader group Sauropterygia, part of Pistosauroidea, the sister taxon to Nothosauroidea within the subgroup Eusauropterygia. This relationship reflects a divergence estimated to have occurred during the Late Triassic, with the earliest definitive plesiosaurian fossils appearing in the Late Triassic (Rhaetian stage) of Europe.^[37]^[38] Within Plesiosauria, modern cladistic analyses recover two primary subgroups: the short-necked Pliosauroidea, encompassing families such as Rhomaleosauridae and Pliosauridae, and the long-necked Plesiosauroidea, which includes diverse families like Microcleididae, Cryptoclididae, and Elasmosauridae. Seminal phylogenetic work by Benson et al. (2010) established a foundational framework for these interrelationships using 66 taxa and 178 characters, emphasizing the role of taxon sampling in resolving plesiosaurian topology. Recent updates, such as those incorporating time-calibrated phylogenies using fossil tip-dating, affirm this bipartition while highlighting rapid diversification in the Early Jurassic. Recent 2025 analyses describe new early-diverging plesiosauroids from the Lower Jurassic of Germany, further resolving basal relationships.^[39]^[40]^[41] Defining synapomorphies of Plesiosauria include hyperphalangy in the limb paddles, characterized by an increased number of phalanges beyond the ancestral count, enhancing hydrodynamic efficiency, and modifications to the gastralia, such as reduction and ventral convergence, which contributed to a streamlined body profile.^[42] These features distinguish plesiosaurs from their nothosauroid relatives and underscore adaptations for fully aquatic lifestyles.^[43] Early classifications often treated the type genus Plesiosaurus as encompassing a wide array of Early Jurassic forms, leading to debates over its monophyly. However, cladistic revisions in the 2010s and 2020s, including detailed reassessments of cranial and postcranial morphology, have demonstrated its paraphyly, resulting in the recognition of distinct genera such as Attenborosaurus, Plesiopterys, and Seeleyosaurus. These splits refine the basal plesiosauroid radiation and highlight the taxonomic diversity of early plesiosaurs.^[44]^[45]

Evolutionary timeline and origins

Plesiosaurs (Plesiosauria) originated during the Late Triassic as a derived clade within the larger group Sauropterygia, which itself evolved from earlier marine reptiles in the Permian and Early Triassic.^[8] The earliest definitive plesiosaurian fossils come from the Rhaetian stage (approximately 208–201 million years ago) in Europe, including a partial skeleton from Germany that exhibits early plesiosaurian characteristics such as elongated cervical vertebrae and paddle-like limbs.^[38] This record indicates that plesiosaurs had already begun diversifying toward the end of the Triassic, likely in shallow marine environments, just prior to the end-Triassic mass extinction event around 201 million years ago.^[38] The Triassic-Jurassic boundary extinction provided ecological opportunities that fueled a major radiation of plesiosaurs during the Early Jurassic, with the long-necked genus Plesiosaurus dominating assemblages in the Hettangian stage (approximately 201–199 million years ago) across European seas.^[46] By the Middle Jurassic, around the Bajocian-Bathonian stages (approximately 171–165 million years ago), short-necked pliosauroids reached their peak diversity and ecological dominance as macropredators, exemplified by Liopleurodon, which attained lengths over 6 meters and featured robust skulls adapted for crushing prey.^[46] This radiation involved rapid increases in body size and cranial robusticity among pliosaurids, marking a shift toward top-predator roles in Mesozoic marine ecosystems.^[46] Phylogenetic analyses place these groups within Plesiosauria, highlighting convergent evolution of body plans across the clade.^[47] In the Cretaceous, plesiosaurs underwent further diversification, particularly in the Late Cretaceous (approximately 100–66 million years ago), where elasmosaurids with extremely long necks (up to 75 vertebrae) and polycotylids with shorter necks and powerful jaws became prominent in shallow epicontinental seas.^[48] Elasmosaurids, such as those from the Santonian-Campanian stages, adapted to filter-feeding or piscivory, while polycotylids radiated in the Cenomanian (around 100–94 million years ago), filling niches as versatile predators.^[48] Toward the end of the Maastrichtian, plesiosaurs faced intensifying competition from rapidly evolving mosasauroids, which exhibited higher rates of morphological evolution and displaced plesiosaurs as apex predators in open marine habitats.^[49] This competitive pressure, combined with the Cretaceous-Paleogene extinction event at 66 million years ago, led to the complete extinction of plesiosaurs.^[49] Recent post-2020 research has refined understanding of plesiosaur evolution, revealing pulsed patterns of diversification tied to environmental shifts such as sea-level fluctuations and oceanic turnover events. For instance, a 2023 study documents the abrupt rise of macropredatory pliosaurids during the Early-Middle Jurassic transition, correlating with eustatic sea-level changes that expanded shallow-water habitats and facilitated adaptive radiations.^[46] These findings fill previous gaps in the timeline by emphasizing episodic bursts of innovation rather than gradual change, particularly during recovery phases after mass extinctions.^[46]

Anatomy and description

Body size and proportions

Plesiosaurs exhibited considerable variation in body size, ranging from small early forms to gigantic late Mesozoic species. The smallest known plesiosaur, Thalassiodracon hawkinsi from the Early Jurassic, measured approximately 2 m in total length, with a trunk length of just 0.68 m serving as a proxy for its compact build.^[50] In contrast, large elasmosaurs from the Late Cretaceous, such as an unnamed Antarctic specimen, reached nearly 12 m in length and weighed between 11.8 and 14.8 tons, making them among the heaviest marine reptiles of their time.^[51] Short-necked pliosaurs also achieved substantial sizes, with species exceeding 10 m in length and mass estimates around 12 tons, exemplified by forms like Pliosaurus.^[46] Body proportions in plesiosaurs diverged markedly between the two primary morphotypes. Long-necked plesiosauroids featured elongated necks composed of numerous cervical vertebrae, up to 72 in Elasmosaurus platyurus, which could extend over 7 m and comprise half or more of the total body length.^[52] Short-necked pliosaurs, conversely, had abbreviated necks with far fewer vertebrae and outsized heads, often with skull lengths approaching 1.5 m, emphasizing a predatory morphology suited to powerful bites.^[46] These proportional differences highlight the adaptive radiation within Plesiosauria, balancing maneuverability and predation strategies in marine environments. Ontogenetic studies from the 2020s, employing osteohistology, indicate allometric scaling in plesiosaur growth, with rapid somatic expansion during early ontogeny followed by proportional shifts in adulthood.^[53] Juveniles often displayed relatively smaller heads and more uniform limb scaling compared to adults, where head size and flipper proportions enlarged disproportionately in macropredatory lineages like pliosaurs. Within Sauropterygia, plesiosaurs attained far greater maximum sizes than ancestral groups such as pachypleurosaurs, which rarely exceeded 1 m in length, underscoring their evolution toward larger aquatic gigantism.^[54]

Skeletal structure

The skull of pliosaurs exhibits a triangular outline, adapted for powerful biting, with conical teeth featuring smooth crowns and sharp tips suitable for piercing prey.^[55] In contrast, plesiosauroids possess a more elongated skull, with a narrow rostrum and reduced overall robustness to facilitate streamlined swimming.^[56] Both morphotypes share large orbits positioned dorsally for effective binocular vision in aquatic environments and a single upper temporal fenestra typical of the euryapsid cranial configuration, which lightens the skull while accommodating jaw adductor muscles.^[56] The vertebral column of plesiosaurs demonstrates specialized adaptations for buoyancy and maneuverability, with cervical hyperelongation primarily resulting from short centra combined with elongated cervical ribs that interlock to extend neck length while maintaining structural integrity.^[18] Dorsal vertebrae are comparatively compact, forming a rigid thoracic region that supports the attachment of flippers and enhances body stability during locomotion.^[57] Caudal vertebrae decrease in size posteriorly, providing a tapered tail that minimizes drag without contributing significantly to propulsion.^[18] Pectoral and pelvic girdles are markedly expanded, featuring broad scapulae and interlocking coracoids that form extensive platforms for limb articulation and muscle anchorage, optimizing force transmission in water.^[58] The limbs are transformed into paddle-like flippers with hyperphalangic digits, where individual rays can incorporate up to 12 phalanges, increasing flipper area for enhanced hydrodynamic efficiency and lift generation.^[59] Recent computed tomography analyses of plesiosaur thoracic regions have illuminated rib cage flexibility, revealing loosely articulated ribs and gastralia that permitted expansive deformation for respiration and body undulation, contrasting earlier assumptions of excessive rigidity in bony elements.^[60]

Soft tissue and integument

Preservation of soft tissues in plesiosaur fossils is exceptionally rare, providing direct evidence of non-skeletal anatomy that complements the more common osseous remains. These preservations, often occurring in fine-grained marine deposits like the Posidonia Shale, reveal details of the integument and internal structures through impressions, mineralization, or cellular traces. Such findings highlight the challenges of soft tissue fossilization in marine reptiles, where rapid burial in anoxic environments was crucial for avoiding decay and scavenging.00016-9) Skin impressions from Jurassic specimens indicate a predominantly smooth, scaleless integument on the body and tail, adapted for hydrodynamic efficiency in aquatic locomotion, with small, non-overlapping scales present on the flippers resembling those of modern sea turtles. A well-preserved Lower Jurassic plesiosaur, Seeleyosaurus guilelmiimperatoris, from the Posidonia Shale of Germany (approximately 183 million years old) shows scale-free skin on the tail, including identifiable melanosomes, keratinocytes with cell nuclei, and the stratum corneum, confirming a smooth texture that likely reduced drag during swimming. Traces of melanophores—pigment cells containing eumelanin—near the skin's outer surface suggest a countershading pattern, with darker dorsal pigmentation for camouflage against underwater light gradients, a common adaptation in marine vertebrates. This distribution of melanophores across body regions supports crypsis in open-water habitats, though the exact coloration remains inferred from melanosome shape and density.00016-9)00016-9)00016-9) Reconstructions of plesiosaur musculature rely on associated soft tissue impressions and biomechanical modeling, particularly for the neck and abdominal regions. Gastroliths (stomach stones) and preserved gut contents, frequently found clustered in the abdominal cavity, imply robust abdominal musculature capable of grinding food in a gizzard-like structure, aiding digestion of bony prey such as fish. In Cryptoclidus eurymerus, a Middle Jurassic plesiosaur, neck musculature reconstructions based on vertebral zygapophyseal facets and ligament attachments demonstrate flexibility primarily in ventral bending (up to 75 degrees) and lateral excursion, enabled by strong hypaxial and epaxial muscles that allowed precise head positioning without excessive torsion. These muscles attached to elongated neural and haemal spines, providing leverage for controlled movements while limiting dorsal extension to about 20 degrees, consistent with the skeletal framework's constraints.00466-9) Evidence of internal organs is scarce but illuminating, with phosphatized or mineralized gut contents offering snapshots of visceral anatomy. In the Early Cretaceous leptocleidian plesiosaur Umoonasaurus demoscyllus from Australia, micro-CT imaging revealed phosphatized stomach contents including at least 17 teleost fish vertebrae and over 60 rounded gastroliths averaging 5 mm in length, positioned posterior to the pectoral girdle and indicating a capacious, muscular stomach for processing prey. These findings, from the 2010s onward, underscore the rarity of such preservations and their role in confirming piscivory, with gastroliths likely facilitating mechanical breakdown and possibly aiding buoyancy regulation. Similar associations in other plesiosaurs, such as elasmosaurs from the Late Cretaceous Pierre Shale, further document fish remains alongside gastroliths, suggesting consistent organ arrangement across taxa.^[61]^[61]^[62] Recent advances have enhanced understanding of flipper soft tissues, filling gaps in limb integument. Exceptional preservations, including trailing-edge impressions, indicate webbing or flexible membranes extending between phalanges, enhancing paddle-like propulsion. While no 2024 Chinese specimens with amber-like preservation are documented, analogous soft tissue details from the aforementioned Jurassic Seeleyosaurus reveal scaled flipper margins with preserved epidermal layers, implying similar webbed structures for improved thrust generation. These insights, derived from UV and CT analyses, emphasize the integument's role in streamlining the skeletal flippers without altering their bony proportions.00016-9)00016-9)

Paleobiology

Diet and feeding mechanisms

Plesiosaurs exhibited diverse feeding strategies that varied between the short-necked pliosaurs and the long-necked plesiosauroids, as inferred from fossilized stomach contents, tooth morphology, and biomechanical analyses. Pliosaurs, such as those in the genus Pliosaurus, were primarily piscivorous or teuthophagous, preying on fish and squid, with occasional evidence of larger vertebrate consumption including other marine reptiles.^[63] Direct evidence from gut contents in Jurassic specimens confirms ingestion of soft-bodied cephalopods and teleost fish, supporting their role as active pursuit predators in Mesozoic marine ecosystems.^[64] Finite element analysis of cranial mechanics in Pliosaurus kevani, a large Upper Jurassic pliosaur, estimates a maximum bite force of up to 48 kN.^[65] In contrast, plesiosauroids, particularly elasmosaurs, displayed more specialized diets, with hypotheses suggesting filter-feeding behaviors alongside piscivory. Stomach contents from Late Cretaceous elasmosaur specimens, such as those from the Pierre Shale, contain small fish remains and numerous gastroliths (stomach stones), which likely aided in grinding ingested prey and facilitating digestion of minute or soft-bodied organisms.^[62] The presence of gastroliths in high volumes supports the idea that some elasmosaurs filtered small planktonic or nektonic prey from water currents, a strategy analogous to modern baleen whales, though direct filter structures remain unpreserved.^[5] This feeding mechanism would have allowed exploitation of lower trophic resources in coastal and open marine environments. Tooth morphology further delineates feeding adaptations across plesiosaur clades. Conical, interlocking teeth in many plesiosauroids were suited for grasping and holding slippery fish or squid, preventing escape during swallowing, while more robust, triangular teeth in certain pliosaurs facilitated crushing of armored prey like ammonites or harder-shelled cephalopods.^[66] Stable isotope analysis of tooth enamel from Maastrichtian plesiosaurs reveals niche partitioning, with elasmosaurs occupying offshore, higher-trophic piscivorous niches (δ¹³C values indicating pelagic foraging) distinct from nearshore mosasaur diets, underscoring dietary specialization amid competition.^[67] As apex predators in many Mesozoic food webs, pliosaurs dominated upper trophic levels, evidenced by rare coprolites containing fish scales and bone fragments attributable to plesiosaur producers in Jurassic lagerstätten.^[64] These fecal remains, alongside bite marks on prey fossils, confirm their predatory dominance, with isotopic and biomechanical data indicating sustained high-energy feeding on mobile, mid-to-high trophic prey throughout their evolutionary history.^[68]

Locomotion and aquatic adaptations

Plesiosaurs utilized their four enlarged limbs, modified into hydrofoils, for propulsion through an underwater flight mechanism involving alternating up-and-down strokes that generated lift-based thrust.^[69] Hydrodynamic simulations have shown that coordinated flapping of all four flippers could produce up to 40% greater efficiency compared to using only the forelimbs, with the hind flippers contributing significantly to overall thrust during steady swimming.^[69] This limb-dominated locomotion minimized drag while enabling maneuverability in marine environments. A 2025 study of preserved skin in a Jurassic plesiosaur reveals smooth, scaleless body skin for reduced drag, with small scales on flippers, enhancing swimming efficiency.^[70] Gait patterns varied between plesiosaur morphotypes, with short-necked forms such as pliosaurs employing subaqueous "galloping" motions—characterized by asynchronous, powerful strokes—for short bursts of acceleration, akin to terrestrial quadrupeds but adapted for aquatic propulsion.^[71] In contrast, long-necked plesiosauroids relied on more synchronized, steady cruising gaits to maintain efficient travel over longer distances, reducing energetic costs associated with their elongated necks.^[72] Speed estimates derived from tail fin evidence and biomechanical models indicate that pliosaurs could achieve maximum sustained speeds of up to 2.5 m/s during pursuits.^[73] Bone microstructure, including specialized foramina in cervical vertebrae, suggests plesiosaurs were capable of diving to depths of approximately 200 m, where high hydrostatic pressures would have influenced their skeletal adaptations for buoyancy control.^[74] The tail generally played a minor role in propulsion for most plesiosaurs, serving primarily for steering rather than thrust generation. However, 2022 analyses of caudal vertebrae indicate greater flexibility in some polycotylids, potentially allowing oscillatory tail movements to supplement flipper-based locomotion during high-speed maneuvers.

Physiology and metabolism

Plesiosaurs exhibited metabolic strategies that have been intensely debated, with evidence pointing toward a mix of ectothermic and endothermic traits. Oxygen isotope analyses of tooth enamel and bone apatite have indicated body temperatures ranging from 35 °C to 39 °C, higher than ambient seawater temperatures and suggesting endothermy.^[75] However, a 2025 reassessment suggests body temperatures around 27 °C, indicating poikilothermic endothermy.^[76] Bone histology reveals rapid growth rates and elevated resting metabolic rates (RMRs) comparable to those of birds, supporting partial or full endothermy. Specifically, quantitative models derived from limb bone microstructure, including flipper elements, show regional endothermy in the appendages, where high vascularization and fibrolamellar bone deposition imply localized heat generation and retention for enhanced locomotory efficiency.^[77] Respiration in plesiosaurs was adapted for an aquatic lifestyle, with external nasal openings positioned dorsally on the skull to facilitate breathing at the water's surface without fully exposing the body. These nares connected to a respiratory system likely featuring large lungs for air storage, enabling prolonged submergence during dives. Evidence from rib and vertebral histology, combined with pathological indicators of decompression syndrome (dysbaric osteonecrosis), suggests plesiosaurs experienced the bends from repeated deep dives, implying apnea durations limited by oxygen stores but sufficient for hunting in mid-water or benthic zones, potentially exceeding 30 minutes based on comparative physiology of modern analogs.^[78]^[79] Sensory adaptations enhanced plesiosaurs' efficiency in dimly lit marine environments. Large orbits, often comprising 20-30% of skull length, accommodated sizable eyes with a broad corneal aperture, optimizing vision in low-light conditions such as deep water or twilight zones. Neural endocast reconstructions and cranial canal analyses further indicate potential electroreception in the elongated snouts of many taxa, where extensive vascular foramina and nerve channels likely supported ampullae-like organs for detecting bioelectric fields from prey, akin to those in modern sharks and platypuses.^[18]^[80] Growth rates in plesiosaurs, inferred from somatic bone histology, were faster than those of extant reptiles but slower than in mammals of comparable size, reflecting an intermediate metabolic strategy. Longitudinal sections of long bones display cyclical laminae with deposition rates of 2-5 μm/day, exceeding typical reptilian values (e.g., <1 μm/day in crocodilians) but below mammalian averages (10-20 μm/day), consistent with sustained but not continuous rapid growth throughout ontogeny.^[77]^[42]

Reproduction and ontogeny

Plesiosaurs exhibited viviparity, giving birth to live young rather than laying eggs, as evidenced by a well-preserved specimen of the polycotylid Polycotylus latipinnis containing a single large embryo positioned head-first in the pelvic region, indicative of internal gestation similar to that in modern cetaceans and ichthyosaurs. This reproductive strategy aligns with a K-selected life history pattern, characterized by low fecundity and substantial parental investment in few, well-developed offspring to enhance survival in marine environments. Although direct embryonic evidence is limited to short-necked plesiosaurians like polycotylids, the anatomical constraints of long-necked elasmosaurids suggest a similar viviparous mode, as egg-laying would be incompatible with their fully aquatic lifestyle and elongated cervical structure. Ontogenetic studies reveal that plesiosaur hatchlings were born at a relatively large size, with rapid post-hatching growth rates documented through bone histology in polycotylids, where fetal long bones show highly vascularized woven-fibered tissue indicative of accelerated development. In elasmosaurids, neck elongation occurred progressively during ontogeny, with juvenile specimens displaying proportionally shorter cervical regions compared to adults, where differential growth of mid-neck vertebrae contributed to extreme lengthening, reaching up to 70 or more cervical vertebrae in mature individuals. Growth rings in plesiosaur limb bones, formed by annual cyclicity, indicate sustained rapid growth in early life followed by deceleration, with sexual maturity estimated at approximately 5–7 years based on the transition to slower deposition rates in histological sections from taxa like Polycotylus. Sexual dimorphism in plesiosaurs is tentatively supported by morphological variation within polycotylids, where analyses of skeletal elements reveal differences between robust and gracile skull forms, potentially reflecting sex-based distinctions in feeding ecology or body size, though ontogenetic variation complicates interpretation. Clutch sizes were likely small, inferred to be 1–2 offspring per pregnancy due to the large embryonic size relative to maternal body dimensions and the single embryo observed in the known gravid specimen, contrasting with the multiple small young typical of oviparous marine reptiles. Plesiosaurs exhibited behaviors inferred primarily from fossil assemblages, trace fossils, and anatomical features preserved in specimens. Hypotheses regarding sociality arise from the discovery of multiple individuals in close association within the Smoky Hill Chalk Member of the Niobrara Formation in western Kansas, where at least three reasonably complete skeletons of Dolichorhynchops osborni have been documented, suggesting possible gregarious behavior or pack hunting strategies to facilitate prey capture in open marine environments.^[81] Further support for coordinated social interactions comes from rare trackway evidence, including a 2023 description of Coneroichnus marinus trackway from the Upper Jurassic-Lower Cretaceous of Italy, which indicates synchronized flipper movements.^[82] Estimates of plesiosaur intelligence are based on endocranial casts derived from CT scans, revealing brain-to-body mass ratios comparable to those of modern crocodilians, which implies a level of cognitive capability suited to basic predatory and navigational demands rather than complex problem-solving. In pliosaurs, a subgroup of short-necked plesiosaurs, endocasts show an enlarged cerebrum relative to other plesiosaurians, suggesting enhanced processing of sensory input for hunting in varied aquatic conditions.^[83] Sensory physiology, including large orbits supported by sclerotic rings, likely aided in detecting prey in low-visibility waters. Pathological evidence points to intraspecific aggression among plesiosaurs, with healed bite marks observed on bones such as the rostrum and flippers of pliosaur specimens like Kronosaurus, indicating competitive interactions over resources or mates.^[84] Additionally, a Middle Jurassic plesiosaur humerus from the Oxford Clay Formation exhibits abnormal bone growth consistent with a neoplasm, such as osteosarcoma, marking one of the earliest known cases of tumors in marine reptiles and highlighting physiological vulnerabilities during aggressive encounters or environmental stresses. Daily activity patterns are inferred from eye morphology, with large sclerotic rings encircling the orbits in many plesiosaur taxa, such as Thalassiodracon hawksini, indicating adaptations for enhanced light sensitivity that support nocturnal foraging to exploit diel prey migrations in the water column.^[85]

Distribution and paleoecology

Temporal and stratigraphic range

Plesiosaurs, members of the clade Plesiosauria, first appeared during the Late Triassic, with the oldest known diagnostic fossils dating to the Rhaetian stage approximately 201 million years ago (Ma).^[42] Their temporal range extended through the Jurassic and into the Late Cretaceous, culminating in the Maastrichtian stage around 66 Ma, after which they went extinct during the Cretaceous-Paleogene mass extinction event.^[86] This span encompasses roughly 135 million years, during which plesiosaurs diversified across marine environments worldwide.^[87] The earliest well-documented appearances occur in the Hettangian stage of the Early Jurassic, marking a radiation following the end-Triassic extinction, though fragmentary remains suggest a pre-Jurassic origin in the Rhaetian.^[88] Diversity peaked during the Albian to Cenomanian stages of the Late Cretaceous, with high taxonomic richness among groups like polycotylids and elasmosaurids, reflecting adaptive radiations in mid-Cretaceous seas.^[87] Following this zenith, plesiosaur diversity declined sharply after the Cenomanian, influenced by oceanic anoxic events and biotic turnovers, though some lineages persisted until the end of the Maastrichtian.^[48] The type species of the genus Plesiosaurus, P. dolichodeirus, represents one of the earliest named plesiosaurs; it was formally described in 1824 based on specimens from Early Jurassic (Sinemurian) strata dating to approximately 199–190 Ma.^[89] Elasmosaurids, a late-surviving plesiosaurian family, include some of the final known representatives, with fossils from Maastrichtian deposits confirming their presence up to about 66 Ma.^[90] Key stratigraphic units preserving plesiosaurs include the Solnhofen Limestone of Late Jurassic (Tithonian) age, which has yielded articulated skeletons of early plesiosauroids, and the Niobrara Chalk Formation of Late Cretaceous (Turonian–Santonian) age, renowned for exceptional fossils of polycotylids and elasmosaurids such as Polycotylus and Elasmosaurus.^[91]^[92] These lagerstätten provide critical windows into plesiosaur morphology and taphonomy across their stratigraphic distribution.

Geographic distribution

Plesiosaur fossils are known from every continent, reflecting their global distribution across Mesozoic marine environments, with particularly rich assemblages from Laurasian and Gondwanan regions. In Europe, the Jurassic period yielded abundant remains, primarily from marine formations in the United Kingdom and Germany, such as the Callovian-age Oxford Clay Formation, which has preserved numerous complete skeletons of cryptocleidoid plesiosaurs. Similarly, the Lower Jurassic Posidonia Shale of southern Germany has provided early-diverging plesiosaur specimens, including those with exceptional soft tissue preservation. These European sites highlight the group's early diversification in the epicontinental seas of the period.^[93]^[94]^[95]^[96] In North America, the most prolific discoveries date to the Cretaceous, centered in the Western Interior Seaway that bisected the continent, where formations like the Campanian Pierre Shale and Niobrara Chalk have yielded diverse elasmosaurid and polycotylid taxa. Jurassic representatives are less common but include cryptocleidoids from the Late Jurassic Morrison Formation in Wyoming and surrounding areas, indicating early incursions into North American waters. This seaway's deposits account for a significant portion of North American plesiosaur diversity, with over a hundred specimens documented. In 2025, a new elasmosaurid genus, Traskasaura sandrae, was described from Late Cretaceous (Campanian) deposits in British Columbia, representing a 12-meter-long specimen with robust teeth adapted for crushing prey.^[97]^[5]^[98]^[31] Gondwanan continents also preserve key plesiosaur records, particularly from Australia and Antarctica, where Cretaceous marine sediments reveal high-latitude adaptations. In Australia, Early Cretaceous sites such as those in the White Cliffs region of New South Wales have produced plesiosaur skeletons from cool-water assemblages, while Antarctic finds from the James Ross Island region, including the Santa Marta and Lopez de Bertodano Formations, include polycotylids and elasmosaurids from the Late Cretaceous. These southern hemisphere discoveries underscore the group's ability to inhabit polar margins.^[99]^[100]^[101] The latitudinal range of plesiosaur fossils spans from subpolar northern sites to Antarctic localities, demonstrating their tolerance for varied climatic regimes during overlapping temporal intervals in the Jurassic and Cretaceous. High-latitude discoveries, such as those from Arctic regions of Canada, have expanded understanding of polar distributions. Preservation is heavily biased toward marine sedimentary deposits, such as chalks, shales, and limestones formed in open-ocean settings, which favored the accumulation and fossilization of these aquatic reptiles while underrepresenting nearshore or freshwater occurrences.^[102]^[5]^[102]

Habitat and environmental preferences

Plesiosauroids, the long-necked members of Plesiosauria, primarily inhabited epipelagic zones of the open ocean, where their elongated necks may have facilitated foraging in the water column. In contrast, pliosaurs, characterized by short necks and robust skulls, favored neritic environments on continental shelves, allowing them to ambush prey in shallower, more productive coastal waters.^[103]^[104] Fossil assemblages frequently associate plesiosaur remains with cephalopods such as ammonites and belemnites, indicating co-occurrence in mid-latitude marine settings rich in these invertebrates, which likely served as prey or ecosystem indicators. Recent modeling suggests that varying ocean oxygen levels significantly influenced plesiosaur distributions, with lower oxygenation in shelf seas potentially restricting access to certain niches during periods of environmental stress.^[105]^[106]^[107] The Jurassic period's warm, epeiric seas provided expansive, temperate habitats that supported high plesiosaur diversity across global epicontinental basins. However, Cretaceous oceanic anoxic events, marked by widespread deoxygenation and warming, reduced habitat suitability and contributed to fluctuations in plesiosaur taxonomic richness by altering prey availability and oxygen gradients in marine ecosystems.^[108]^[109] Stable isotope analyses of tooth enamel from Maastrichtian elasmosaurs yield δ¹³C values ranging from -12.50‰ to -10.16‰, overlapping with those of mosasaurs and suggesting similar foraging in nearshore to offshore settings rather than distinct niche partitioning.^[67]

Cultural significance

In popular media and art

Plesiosaurs have long captured the imagination in 19th-century art, where early restorations frequently portrayed them in terrestrial or amphibious poses due to limited understanding of their anatomy and locomotion. Following the 1824 description of Plesiosaurus dolichodeirus by William Daniel Conybeare, based on a specimen discovered by Mary Anning in 1823, illustrations often showed these reptiles crawling on land with their flippers splayed outward, emphasizing a semi-aquatic lifestyle akin to seals or crocodiles.^[110] These depictions, such as those in early scientific publications, were later revised as evidence accumulated for their fully aquatic adaptations; by 1854, Benjamin Waterhouse Hawkins' life-sized concrete models at London's Crystal Palace depicted plesiosaurs swimming in artificial lakes, marking a shift toward more accurate aquatic representations.^[111]^[112] In film and television, plesiosaurs often appear as dramatic sea monsters, frequently exaggerating their connection to cryptozoological legends like the Loch Ness Monster. The BBC's 2003 documentary Sea Monsters: A Prehistoric Adventure featured plesiosaurs as agile hunters in Jurassic seas, using CGI to illustrate their predatory behaviors based on fossil evidence. Similarly, the 2015 film Jurassic World included a spectacular aquatic feeding sequence featuring a massive, short-necked marine reptile (a mosasaur) that evoked imagery of prehistoric sea monsters, including plesiosaurs, blending popular myths with cinematic spectacle to heighten the prehistoric thriller elements.^[113] Literature has further embedded plesiosaurs in cultural narratives, from classic adventure tales to modern pseudoscience. Jules Verne's 1864 novel Journey to the Center of the Earth vividly describes a fierce battle between a plesiosaur and an ichthyosaur in an subterranean ocean, portraying the reptile as a living emblem of ancient wonders and inspiring generations of speculative fiction. In contemporary cryptozoology, plesiosaurs are central to myths of surviving relics, particularly as the basis for Loch Ness Monster sightings, with books and documentaries perpetuating the idea of hidden populations in isolated waters despite lacking empirical support.^[114]^[115] Persistent misconceptions, such as plesiosaurs walking on land or thriving in freshwater environments like modern lakes, stem from these early artistic and literary influences but have been effectively debunked through 2020s paleontological outreach efforts. Museum exhibits and educational programs, including those by the Natural History Museum, emphasize biomechanical analyses showing flipper-based swimming as their primary locomotion, incapable of supporting terrestrial movement, while clarifying that most species were strictly marine, countering Loch Ness survival claims with isotopic and fossil data.^[111]

Scientific and educational impact

Plesiosaurs have played a pivotal role in advancing paleontology, particularly through their contributions to biostratigraphy and theories of marine reptile evolution. Fossil records of plesiosaurs, spanning the Late Triassic to Late Cretaceous, have been instrumental in refining stratigraphic correlations within Mesozoic marine deposits, enabling precise dating of Jurassic and Cretaceous rock layers based on their taxonomic distributions and turnover events.^[116] For instance, analyses of Jurassic marine reptile assemblages, including plesiosaurs, have illuminated faunal turnovers at the Early-Middle Jurassic boundary, supporting models of evolutionary radiation and extinction dynamics in aquatic ecosystems.^[116] These findings have bolstered broader theories on the adaptive radiation of Sauropterygia, the clade encompassing plesiosaurs, by highlighting convergent evolution with other marine groups like ichthyosaurs and mosasaurs.^[117] In education, plesiosaur fossils serve as cornerstone exhibits in museums, fostering public understanding of prehistoric life. The Natural History Museum in London displays a complete Plesiosaurus dolichodeirus specimen discovered by Mary Anning in 1823, which illustrates marine reptile anatomy and Jurassic paleoenvironments, drawing millions of visitors annually to engage with paleontological concepts. In 2023, the bicentennial of Anning's plesiosaur discovery was marked by various exhibitions and publications, further emphasizing her role in paleontology.^[10]^[118] Complementing physical displays, virtual reality (VR) models developed in the 2020s have enhanced interactive learning; for example, Discovery Education's Plesiosaur Encounter TimePod adventure allows students to explore 3D reconstructions of plesiosaur habitats, linking fossil evidence to evolutionary processes and fossilization mechanics.^[119] Such tools promote conceptual grasp of deep time and biodiversity without requiring physical specimens. Plesiosaur research has driven innovations in imaging and biomechanical analysis, influencing technological applications beyond paleontology. Micro-computed tomography (CT) scans of plesiosaur limbs have enabled detailed 3D modeling of muscle attachments and forces, revealing propulsion mechanisms in flipper-based swimming and advancing finite element analysis for extinct taxa.^[120] These methods, initially refined on plesiosaur specimens, have improved non-invasive imaging protocols now used in vertebrate biomechanics studies. Recent conferences, such as the Society of Vertebrate Paleontology's 84th Annual Meeting in 2024, have included presentations on plesiosaur phylogeny and new taxa within Sauropterygia.^[121] The legacy of Mary Anning, who unearthed the first recognized plesiosaur skeleton, extends to public engagement and discussions on diversity in STEM fields. Her breakthroughs, despite facing gender-based exclusion from scientific societies, have inspired initiatives highlighting underrepresented voices in paleontology, emphasizing how early female contributions shaped modern research practices.^[10]^[122] Anning's story is routinely invoked in educational programs to promote inclusivity, underscoring the societal barriers overcome in advancing knowledge of marine reptiles.^[122]

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Feb 19, 2024 · There were 2 plesiosaur fossils with soft tissue imprints described in the 20th century: the holotype of Microleidus brachypterygius and a ...<|separator|>
[60]
Full article: Investigating gut contents of the leptocleidian plesiosaur ...
Apr 17, 2023 · These comprise 17 vertebrae from an unidentified teleost, together with at least 60 rounded gastroliths averaging about 5 mm in maximum length.Missing: phosphatized | Show results with:phosphatized
[61]
An Elasmosaur with Stomach Contents and Gastroliths from the ...
Sep 22, 2025 · ... Gastroliths, or stomach stones, are routinely found associated with elasmosaurs and other long necked plesiosaurs (Andrews, 1910Andrews, , ...Missing: muscle | Show results with:muscle
[62]
Plasticity and Convergence in the Evolution of Short-Necked ...
Jun 5, 2017 · Short-necked plesiosaurs iteratively evolved a large bodied, long-snouted morphology, suggesting the iterative colonization of a piscivorous ...
[63]
Diet and senses - Plesiosaur Directory
The presence of gastroliths is common in plesiosaurs. Pollard (1990) noted that plesiosauroid stomach contents “usually contain gastroliths” (fig 9), and ...Missing: phosphatized | Show results with:phosphatized<|separator|>
[64]
Functional anatomy and feeding biomechanics of a giant Upper ...
Jun 13, 2014 · Pliosaurs were among the largest predators in Mesozoic seas, and yet their functional anatomy and feeding biomechanics are poorly understood ...Missing: piscivorous autophagous 2019
[65]
Tooth Morphology and Prey Preference of Mesozoic Marine Reptiles
They are short cylindrical pegs, wider than they are high, and are used for crushing oysters and clams (Walker, 1975). Thus, as one would expect, teeth used on ...
[66]
Stable isotopes, niche partitioning and the paucity of elasmosaur ...
Jun 30, 2016 · Stable isotopes, niche partitioning and the paucity of elasmosaur remains in the Maastrichtian type area - Volume 96 Issue 1.
[67]
(PDF) Bottom-Feeding Plesiosaurs - ResearchGate
Aug 6, 2025 · Some mosasaurs have their stomach contents preserved, providing direct and unambiguous evidence of diet. The results show a relatively clear ...
[68]
The four-flipper swimming method of plesiosaurs enabled efficient ...
Aug 30, 2017 · We show that plesiosaur hind flippers generated up to 60% more thrust and 40% higher efficiency when operating in harmony with their forward counterparts.<|separator|>
[69]
Fluid dynamics, scaling laws and plesiosaur locomotion - IOPscience
Here we propose a new approach to studying plesiosaur locomotion based on universal scaling laws in fluid dynamics.
[70]
Rethinking the four-wing problem in plesiosaur swimming using bio ...
Oct 28, 2024 · We focus on plesiosaurs, an extinct aquatic reptile group which has two pairs of flipper-shaped limbs, and demonstrate that a highly optimised, ...
[71]
(PDF) Plesiosaur Swimming as Interpreted from Skeletal Analysis ...
Aug 5, 2025 · The long-necked plesiosauroids were probably slow swimmers and relied on a sneak attack to capture prey. The pliosauroids, with shorter necks ...
[72]
New study shows how long-necked plesiosaurs swam - ZME Science
Jul 5, 2017 · “Studies have shown an optimal swimming speed for plesiosaurs of about 0.4 m/s (1.44 km/h) to a maximum sustained speed of about 2.5 m/s (9 ...
[73]
[PDF] Foramina in plesiosaur cervical centra indicate a specialized ...
Dec 19, 2017 · All plesiosaurian cervical vertebrae show a pair of large foramina on the ventral surface of the vertebral cen- tra (Romer, 1956). These ...Missing: hyperelongation | Show results with:hyperelongation<|separator|>
[74]
Regulation of body temperature by some Mesozoic marine reptiles
Jun 11, 2010 · We tested the thermal status of ichthyosaurs, plesiosaurs, and mosasaurs by comparing the oxygen isotope compositions of their tooth phosphate ...Missing: bradymetabolic | Show results with:bradymetabolic
[75]
Quantitative histological models suggest endothermy in plesiosaurs
Jun 6, 2018 · Our models reveal bone growth rates and RMRs for plesiosaurs that are in the range of birds, suggesting that plesiosaurs were endotherm.
[76]
(PDF) Decompression syndrome in plesiosaurs (Sauropterygia
Aug 10, 2025 · Avascular necrosis, a condition arising from decompression syndrome in diving organisms, is common in Cretaceous marine turtles and other ...<|control11|><|separator|>
[77]
Cumulative sperm whale bone damage and the bends - PubMed
Dec 24, 2004 · Diving mosasaurs, plesiosaurs, and humans develop dysbaric osteonecrosis from end-artery nitrogen embolism ("the bends") in certain bones.
[78]
New ancient sea reptile found in Germany – the earliest of its kind
Aug 28, 2017 · Internal channels in the upper jaws might have housed nerves linked to pressure receptors or electroreceptors on the outside of the snout that ...
[79]
First records of plesiosaur remains in the lower Smoky Hill Chalk ...
Aug 5, 2025 · There are only three reasonably complete plesiosaur skeletons (all Dolichorhynchops osborni) known from the Smoky Hill Chalk in Kansas. All ...
[80]
Plesiosauria remains from the Barremian of Morella (Castellón ...
New plesiosaur remains are described in Late Barremian from Morella, Spain. ... CONEROICHNUS MARINUS ICHNOGENUS ET ICHNOSPECIES NOV., A FOSSIL TRACKWAY OF ...
[81]
Complex rostral neurovascular system in a giant pliosaur
Aug 10, 2025 · Pliosaurs were a long-lived, ubiquitous group of Me-sozoic marine predators attaining large body sizes (up to 12 m).Missing: cerebrum | Show results with:cerebrum
[82]
Cranial anatomy, taxonomic implications and palaeopathology of an ...
Aug 6, 2025 · Overall, the morphology is slender, lacking significant mediolateral expansion, and lacking the 'rostral constriction' that is present around ...
[83]
Plesiosaurian Evolution and Adaptations - Darwin's Door
Jan 1, 2023 · It is thought that Plesiosauria, a member of the larger clade Sauropterygia, evolved in the latest Triassic from more basal sauropterygians.
[84]
Maastrichtian plesiosaurs from northern Patagonia - ScienceDirect
They were found in the uppermost levels of the Jagüel Formation (upper Maastrichtian). One of the specimens was found only 0.3 m below the Cretaceous/Paleogene ...
[85]
Mesozoic marine tetrapod diversity: mass extinctions and temporal ...
Nov 18, 2009 · Both trends rise to a peak around the Albian–Cenomanian. They then decline until the Coniacian before increasing to a Campanian–Maastrichtian ...
[86]
Cranial anatomy of a new plesiosaur genus from the lowermost Lias ...
Many features of the 3-dimensional, matrix-free skull are seemingly plesiomorphic in accord with the early, probably latest Rhaetian, stratigraphic position of ...
[87]
Plesiosaurus - Plesiosaur Directory
The type species (P. dolichodeirus) was named a few years later (Conybeare 1824) following the discovery of a complete articulated specimen (NHMUK 22656) by ...<|control11|><|separator|>
[88]
Elasmosaur remains from the Maastrichtian type area, and a review ...
Aug 7, 2025 · Isolated skeletal remains of elasmosaurid plesiosaurs are described from the upper Upper Maastrichtian of the type area of that stage and ...
[89]
Marine reptiles | Paleontology Class Notes - Fiveable
Notable fossil localities include the Jurassic Coast of England, the Solnhofen Limestone of Germany, and the Niobrara Chalk of North America; The Triassic ...
[90]
[PDF] PLESIOSAURIA) IN THE NIOBRARA CHALK OF WESTERN KANSAS
ABSTRACT. The Niobrara Chalk, including the Fort Hays Limestone and Smoky Hill Chalk, was deposited during a period of high sea levels.Missing: Solnhofen | Show results with:Solnhofen<|control11|><|separator|>
[91]
A truly gigantic pliosaur (Reptilia, Sauropterygia) from the ...
In the Middle Jurassic (Callovian) the pliosaur Liopleurodon from the Peterborough Member of the Oxford Clay Formation is credited with a length of around 9.1 m ...
[92]
A new plesiosaurian from the Jurassic–Cretaceous transitional ...
The skeleton of PMO 224.248 is well-preserved and fully articulated, with the exception of the skull, some dorsal vertebrae and distal phalangeal elements (Fig.
[93]
Skin, scales, and cells in a Jurassic plesiosaur - ScienceDirect.com
Mar 10, 2025 · A new polycotylid plesiosaur with extensive soft tissue preservation from the early Late Cretaceous of northeast Mexico. Bol. Soc. Geol. Mex ...Missing: discoveries | Show results with:discoveries
[94]
Early-diverging plesiosaurs from the Pliensbachian (Lower Jurassic ...
Nov 26, 2024 · Here, we describe two previously unreported lower Pliensbachian plesiosaur occurrences that originate from two sites located in North Rhine-Westphalia, Germany.
[95]
A new genus of small polycotylid plesiosaur from the Upper ...
Revised diagnosis. Polycotylid plesiosaur subfamily possessing the following synapomorphies: jugal shortened to terminate near posterior. Preservation. Most ...
[96]
[PDF] Osteology of the cryptocleidoid plesiosaur Tatenectes laramiensis ...
... Morrison Formation. The marine sediments of Jurassic age from southeastern Wyoming were originally named the “Shirley Stage” by. Knight in 1900. The name ...
[97]
Marine reptiles from the Lower Cretaceous (Aptian) deposits of ...
Marine reptiles from the Lower Cretaceous (Aptian) deposits of White Cliffs, southeastern Australia: implications of a high latitude, cold water assemblage.
[98]
First record of Polycotylidae (Sauropterygia, plesiosauria) from the ...
The material was collected from the Alpha Member of the Santa Marta Formation (upper Coniacian–lower Campanian) on James Ross Island, Antarctic Peninsula. The ...Missing: key | Show results with:key
[99]
A Late Jurassic plesiosaur in Antarctica: Evidence of the dispersion ...
We describe a newly recovered plesiosaur specimen from the Ameghino (= Nordensköld) Formation, Antarctic Peninsula, the first Jurassic plesiosaur from ...
[100]
The completeness of the fossil record of plesiosaurs, marine reptiles ...
Here, we conduct the first detailed assessment of the quality of the plesiosaur fossil record. Data was compiled for 178 specimens representing 114 valid ...Missing: 20th | Show results with:20th
[101]
New plesiosaur records from the Lower Cretaceous of the Neuquén ...
Plesiosaurs constitute a monophyletic group of cosmopolitan marine reptiles encompassing the Late Triassic–Late Cretaceous time interval (Ketchum and Benson ...
[102]
Plesiosaurs and Pliosaurs - The Sea Serpents - ThoughtCo
Jan 31, 2019 · Plesiosaurs (Greek for "almost lizards") were large, long-necked, four-flippered marine reptiles that paddled their way through the oceans, ...
[103]
Plesiosaur remains associated with a rich marine fauna from the ...
Lechites (orthocone), the most abundant taxon, probably inhabited epipelagic, distal paleoenvironments. ... neritic paleoenvironments. These forms could ...
[104]
[PDF] An Early Cretaceous plesiosaur from Ellesmere Island, Nunavut ...
Dec 2, 2024 · A plesiosaur specimen collected from Ellesmere Island (Nunavut, Arctic Canada) by Danish geologist Johannes Troelsen.
[105]
Ocean's loss of oxygen caused massive Jurassic extinction: Could it ...
Jun 26, 2024 · Volcanic activity pumped out CO2, warming oceans and lowering their oxygen levels. The findings may foretell the impact climate change and ...
[106]
A Late Jurassic plesiosaur in Antarctica: Evidence of the dispersion ...
These and all subsequent Antarctic plesiosaur discoveries have occurred in the James Ross Basin at the northeastern tip of the Antarctic Peninsula (Fig. 1) ...
[107]
Early Cretaceous life, climate and anoxia - ScienceDirect
Humid conditions and the corresponding tendency to develop dys- to anaerobic conditions in deeper ocean waters led to phases of accelerated extinction in oceans ...
[108]
Plesiosaurs on the rocks: the terrestrial capabilities of four-flippered ...
Jan 25, 2019 · The idea of plesiosaurians leaving water has been strongly tied to historic uncertainty about their reproductive habits.Missing: Waterhouse Hawkins pose
[109]
The world's first dinosaur park: what the Victorians got right and wrong
The Crystal Palace Dinosaurs were the creation of one of the best-known natural history sculptors of his time, Benjamin Waterhouse Hawkins (1807-1894).
[110]
Fiction - Plesiosaur Directory
Here's a selection of notable plesiosaur appearances in film and television. Possibly the first ever depiction of a plesiosaur on screen was in the original ...Missing: media | Show results with:media
[111]
A Journey to the Center of the Earth - Chapter XXXIII. A Battle of ...
"The other is a plesiosaurus (almost lizard), a serpent, armoured with the carapace and the paddles of a turtle; he is the dreadful enemy of the other." Hans ...
[112]
Sea Monster Sightings and the 'Plesiosaur Effect' - Tetrapod Zoology
Apr 28, 2019 · Regular readers of this blog will almost certainly be aware of what are most sensibly termed sea monster accounts.
[113]
Refining the marine reptile turnover at the Early–Middle Jurassic ...
Feb 22, 2021 · This turnover saw the demise of early neoichthyosaurians, rhomaleosaurid plesiosaurians and early plesiosauroids in favour of ophthalmosaurid ichthyosaurians.
[114]
[PDF] GROWTH RATES AND METABOLISM IN A CLADE OF ...
... aquatic Mesozoic marine reptiles. Over their 160 million years of evolution, the clade evolved a streamlined body plan with paddle-like limbs, convergent ...
[115]
Plesiosaur Encounter: A New TimePod Adventure
Highly interactive with beautiful cinematics and gripping gameplay, this 3D virtual field trip links out to learning about evolution, fossilization, ...Missing: VR 2020s
[116]
Determination of muscle strength and function in plesiosaur limbs
Jun 3, 2022 · The flippers of plesiosaurs were twisted along the flipper length axis by extensors and flexors that originated from the humerus and femur as ...
[117]
[PDF] SVP 84th ANNUAL MEETING - Society of Vertebrate Paleontology
Oct 30, 2024 · The SVP 84th Annual Meeting is in Minneapolis, Minnesota, USA, at the Hyatt Regency from October 30 to November 2, 2024.
[118]
Mary Anning: The First Female Paleontologist - STEAM News
Oct 18, 2024 · The first-ever discovery of a dinosaur ... Mary Anning had made a huge impact in the world of science, but her work lacked recognition.