Mosasaurs comprise a group of extinct, large marine reptiles from the Late Cretaceous. Their first fossil remains were discovered in a limestone quarry at Maastricht on the Meuse in 1764. They belong to the order Squamata, which includes lizards and snakes.
Hypselosaurus is a dubious genus of titanosaurian sauropod that lived in southern France during the Late Cretaceous, approximately 70 million years ago in the early Maastrichtian. Hypselosaurus was first described in 1846, but was not formally named until 1869, when Phillip Matheron named it under the binomial Hypselosaurus priscus. The holotype specimen includes a partial hindlimb and a pair of caudal vertebrae, and two eggshell fragments were found alongside these bones. Because of the proximity of these eggshells to the fossil remains, many later authors, including Matheron and Paul Gervais, have assigned several eggs from the same region of France all to Hypselosaurus, although the variation and differences between these eggs suggest that they do not all belong to the same taxon. Hypselosaurus has been found in the same formation as the dromaeosaurids Variraptor and Pyroraptor, the ornithopod Rhabdodon, and the ankylosaurian Rhodanosaurus, as well as indeterminate bones from other groups.
Dinosaur eggs are the organic vessels in which a dinosaur embryo develops. When the first scientifically documented remains of non-avian dinosaurs were being described in England during the 1820s, it was presumed that dinosaurs had laid eggs because they were reptiles. In 1859, the first scientifically documented dinosaur egg fossils were discovered in France by Jean-Jacques Poech, although they were mistaken for giant bird eggs.
The Lopez de Bertodano Formation is a geological formation in the James Ross archipelago of the Antarctic Peninsula. The strata date from the end of the Late Cretaceous to the Danian stage of the lower Paleocene, from about 70 to 65.5 million years ago, straddling the Cretaceous-Paleogene boundary.
Elongatoolithus is an oogenus of dinosaur eggs found in the Late Cretaceous formations of China and Mongolia. Like other elongatoolithids, they were laid by small theropods, and were cared for and incubated by their parents until hatching. They are often found in nests arranged in multiple layers of concentric rings. As its name suggests, Elongatoolithus was a highly elongated form of egg. It is historically significant for being among the first fossil eggs given a parataxonomic name.
Macroelongatoolithus is an oogenus of large theropod dinosaur eggs, representing the eggs of giant caenagnathid oviraptorosaurs. They are known from Asia and from North America. Historically, several oospecies have been assigned to Macroelongatoolithus, however they are all now considered to be a single oospecies: M. carlylensis.
Macroolithus is an oogenus of dinosaur egg belonging to the oofamily Elongatoolithidae. The type oospecies, M. rugustus, was originally described under the now-defunct oogenus name Oolithes. Three other oospecies are known: M. yaotunensis, M. mutabilis, and M. lashuyuanensis. They are relatively large, elongated eggs with a two-layered eggshell. Their nests consist of large, concentric rings of paired eggs. There is evidence of blue-green pigmentation in its shell, which may have helped camouflage the nests.
Phaceloolithus is an oogenus of dinosaur egg found in the Fenshui'ao Formation of the Dongting Basin of the Hunan Province of China. The eggs have a subspherical shape, measuring up to 168 mm on the long axis, and having a very thin shell.
Continuoolithus is an oogenus of dinosaur egg found in the late Cretaceous of North America. It is most commonly known from the late Campanian of Alberta and Montana, but specimens have also been found dating to the older Santonian and the younger Maastrichtian. It was laid by an unknown type of theropod. These small eggs are similar to the eggs of oviraptorid dinosaurs, but have a distinctive type of ornamentation.
Egg fossils are the fossilized remains of eggs laid by ancient animals. As evidence of the physiological processes of an animal, egg fossils are considered a type of trace fossil. Under rare circumstances a fossil egg may preserve the remains of the once-developing embryo inside, in which case it also contains body fossils. A wide variety of different animal groups laid eggs that are now preserved in the fossil record beginning in the Paleozoic. Examples include invertebrates like ammonoids as well as vertebrates like fishes, possible amphibians, and reptiles. The latter group includes the many dinosaur eggs that have been recovered from Mesozoic strata. Since the organism responsible for laying any given egg fossil is frequently unknown, scientists classify eggs using a parallel system of taxonomy separate from but modeled after the Linnaean system. This "parataxonomy" is called veterovata.
This timeline of egg fossils research is a chronologically ordered list of important discoveries, controversies of interpretation, taxonomic revisions, and cultural portrayals of egg fossils. Humans have encountered egg fossils for thousands of years. In Stone Age Mongolia, local peoples fashioned fossil dinosaur eggshell into jewelry. In the Americas, fossil eggs may have inspired Navajo creation myths about the human theft of a primordial water monster's egg. Nevertheless, the scientific study of fossil eggs began much later. As reptiles, dinosaurs were presumed to have laid eggs from the 1820s on, when their first scientifically documented remains were being described in England. In 1859, the first scientifically documented dinosaur egg fossils were discovered in southern France by a Catholic priest and amateur naturalist named Father Jean-Jacques Poech, however he thought they were laid by giant birds.
Egg paleopathology is the study of evidence for illness, injury, and deformity in fossilized eggs. A variety of pathological conditions afflicting eggs have been documented in the fossil record. Examples include eggshell of abnormal thickness and fossil eggs with multiple layers of eggshell. The identification of egg paleopathologies is complicated by the fact that even healthy eggs can be modified during or after fossilization. Paleontologists can use techniques like cathodoluminescence or thin sectioning to identify true paleopathologies in fossil eggs. Despite the diversity of paleopathologies known from fossil eggs, the vast majority of conditions known to afflict modern eggs have not yet been seen among fossils.
Egg taphonomy is the study of the decomposition and fossilization of eggs. The processes of egg taphonomy begin when the egg either hatches or dies. Eggshell fragments are robust and can often travel great distances before burial. More complete egg specimens gradually begin to fill with sediment, which hardens as minerals precipitate out of water percolating through pores or cracks in the shell. Throughout the fossilization process the calcium carbonate composing the eggshell generally remains unchanged, allowing scientists to study its original structure. However, egg fossils buried under sediments at great depth can be subjected to heat, pressure and chemical processes that can alter the structure of its shell through a process called diagenesis.
Reptile egg fossils are the fossilized remains of eggs laid by reptiles. The fossil record of reptile eggs goes back at least as far as the Early Permian. However, since the earliest reptile eggs probably had soft shells with little preservation potential, reptilian eggs may go back significantly farther than their fossil record. Many ancient reptile groups are known from egg fossils including crocodilians, dinosaurs, and turtles. Some ancient reptiles are known to have given live birth and are therefore not anticipated to have left behind egg fossils.
Coralloidoolithus is an oogenus of dinosaur egg from the Tiantai Basin in Zhejiang Province, containing a single known oospecies C. shizuiwanensis. Formerly, it was classified in the oogenus Paraspheroolithus; however, it was considered sufficiently different to be classified in its own genus. C. shizuiwanensis is similar to Stalicoolithus, leading to their classification in the same family, Stalicoolithidae.
Elongatoolithidae is an oofamily of fossil eggs, representing the eggs of oviraptorosaurs. They are known for their highly elongated shape. Elongatoolithids have been found in Europe, Asia, and both North and South America.
Guegoolithus is an oogenus of fossil egg from the early Cretaceous of Spain. It is classified in the oofamily Spheroolithidae, and was probably laid by an ornithopod dinosaur.
Incognitoolithus is an oogenus of medioolithid fossil bird egg. It is notable for bearing evidence of predation, possibly from a bird pecking the eggshell.
Pachycorioolithus is an oogenus of small, thin-shelled fossil egg from the early Cretaceous in China. It probably belongs to a bird, though there is a possibility the parent was a non-avian theropod. It was named in 2016, based on a single specimen found in Zhejiang.
Plagioolithus is an oogenus of fossil egg. It is from the Early Cretaceous of Japan. It was probably laid by a bird, making it the oldest known fossil bird egg.
