Research Article

Terrestrial Origin of Viviparity in Mesozoic Marine Reptiles Indicated by Early Triassic Embryonic Fossils

  • Ryosuke Motani,

    Affiliation: Department of Earth and Planetary Sciences, University of California, Davis, Davis, California, United States of America

  • Da-yong Jiang mail,

    Affiliations: Laboratory of Orogenic Belt and Crustal Evolution, Ministry of Education, Department of Geology and Geological Museum, Peking University, Beijing, People’s Republic of China, State Key Laboratory of Palaeobiology and Stratigraphy (Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences), Nanjing, Jiangsu Province, People’s Republic of China

  • Andrea Tintori,

    Affiliation: Dipartimento di Scienze della Terra, Università degli Studi di Milano, Via Mangiagalli, Milano, Italy

  • Olivier Rieppel,

    Affiliation: Center of Integrative Research, The Field Museum, Chicago, Illinois, United States of America

  • Guan-bao Chen

    Affiliation: Department of Research, Anhui Geological Museum, Hefei, Anhui Province, People’s Republic of China

  • Published: February 12, 2014
  • DOI: 10.1371/journal.pone.0088640
  • Featured in PLOS Collections


Viviparity in Mesozoic marine reptiles has traditionally been considered an aquatic adaptation. We report a new fossil specimen that strongly contradicts this traditional interpretation. The new specimen contains the oldest fossil embryos of Mesozoic marine reptile that are about 10 million years older than previous such records. The fossil belongs to Chaohusaurus (Reptilia, Ichthyopterygia), which is the oldest of Mesozoic marine reptiles (ca. 248 million years ago, Early Triassic). This exceptional specimen captures an articulated embryo in birth position, with its skull just emerged from the maternal pelvis. Its headfirst birth posture, which is unlikely to be a breech condition, strongly indicates a terrestrial origin of viviparity, in contrast to the traditional view. The tail-first birth posture in derived ichthyopterygians, convergent with the conditions in whales and sea cows, therefore is a secondary feature. The unequivocally marine origin of viviparity is so far not known among amniotes, a subset of vertebrate animals comprising mammals and reptiles, including birds. Therefore, obligate marine amniotes appear to have evolved almost exclusively from viviparous land ancestors. Viviparous land reptiles most likely appeared much earlier than currently thought, at least as early as the recovery phase from the end-Permian mass extinction.


Viviparity allows maternal maintenance of the embryonic environment, and is known across bony fishes, elasmobranchs, amphibians, reptiles, and mammals [1]. It independently evolved at least 141 times in the vertebrates, of which 108 are found in squamate reptiles [2]. The oldest fossil record of viviparity in vertebrates belongs to a placoderm 'fish' from the Devonian, approximately 380 million years old [3], but that for amniotes is younger at about 280 million years old [4], in a Permian marine reptile Mesosaurus that lived in an inland sea [5]. Viviparity is considered mostly a terrestrial feature in amniotes [6]. However, viviparity is also a necessary feature in obligatory marine amniotes, such as some Mesozoic marine reptiles [7][13], which could not walk on land or lay eggs in the sea [8], [9]. This raises the question of whether viviparity in obligatory marine Mesozoic reptiles was inherited from their respective terrestrial ancestors, or evolved after each lineage invaded the sea as an aquatic adaptation, as has traditionally been thought.

Ichthyopterygia is a group of Mesozoic marine reptiles known for a fish-shaped body profile [14] and enormous eyes [15] in derived forms. They are also known for being viviparous: at least six ichthyopterygian genera, spanning the Middle Triassic to Early Cretaceous, have fossil records of embryos [11][13], [16], [17]. However, the reproductive biology of the earliest ichthyopterygians, which lived in the late Early Triassic (ca. 251–247 million years ago), was not known.

Chaohusaurus is one of the three basal ichthyopterygian genera that unequivocally lived during the Early Triassic [18]. Our recent field excavation [19] yielded more than 80 new skeletons, greatly advancing our knowledge of the earliest ichthyopterygians—there were less than 20 skeletons known of the three genera before. Chaohusaurus is not the most basal of the Early Triassic ichthyopterygians [18] but our field survey revealed that the genus had the oldest stratigraphic record of the three (figure 1), extending back at least to the early-middle Spathian (Procolumbites Zone), some 248 million years ago [4]. Among the 80 specimens was a partial skeleton that contained embryos, AGM I-1 (Anhui Geological Museum, Hefei, China), which uncovers for the first time the reproductive strategy of the earliest marine reptiles of the Mesozoic (figure 2).


Figure 1. Stratigraphy and phylogeny of the earliest ichthyopterygians, with a reconstruction of the typical birth posture in derived members.

Chaohusaurus has the oldest stratigraphic record of the three Early Triassic genera. Star indicates the stratigraphic position of the present specimen. Time scale was drawn using TS Creator 6.1.2 that follows [4]. See fig. S1 for a high resolution image.


Figure 2. The maternal specimen with three embryos.

Color coding indicates: black, maternal vertebral column, including neural and haemal spines; blue, maternal pelvis and hind flipper; green, maternal ribs and gastralia. Embryos 1 and 2 are in orange and yellow, respectively, whereas neonate 1 is in red. Scale bar is 1 cm. Abbreviations: i-v, metatarsals; 4, fourth distal tarsal; a, astragalus; c, calcaneum; cr, caudal rib; cv, caudal vertebra; d, dentary; fe, femur; fi, fibula; h, haemal spine; il, ilium; is, ischium; pb, pubis; pm, premaxilla; sr, sacral rib; sv, sacral vertebra; and ti, tibia. See fig. S2 for a high resolution image.


Materials and Methods


The specimens used in this study (AGM I-1, AGM CHS-5, and AGM CH-628-22) were all collected from a fossil quarry in south Majiashan, Chaohu, Anhui, China, through a joint excavation by AGM, Peking University, University of California, Davis, Università degli studi di Milano, and the Field Museum, with permits from the Ministry of Land and Resources of the People’s Republic of China. The Spathian Nanlinghu formation is exposed in the quarry. All specimens are accessioned at the Anhui Geological Museum in Hefei City, Anhui Province, China. All three specimens are from near the bottom of the Subcolumbites zone of the Middle Spathian (Lower Triassic).

The specimen with embryos (AGM I-1) was initially collected while still concealed in the rock as a 'by-catch' of a specimen of the predatory fish Saurichthys that was exposed on the same slab (AGM I-2). It was later uncovered in the laboratory by our preparator, so there is no possibility of forgery. It is unlikely that the Saurichthys on the same slab was hunting for a newborn Chaohusaurus. It did not occupy the same time horizon with the Chaohusaurus individuals because there are a few laminae of mudstones between the two.


The three new specimens are assigned to Chaohusaurus for the following reasons. Most importantly, Chaohusaurus is the only ichthyopterygian to exhibit delayed ossification of carpals and tarsals relative to metacarpals/metatarsals and phalanges, and this feature is clearly present in all of the specimens used in this study. The three specimens further exhibit the typical dental morphology, vertebral count, and the unique hypophalangeal flippers of Chaohusaurus. The current taxonomy holds that Chaohusaurus geishanensis is the only species within the genus [18], [20], although specific taxonomy may require a revision as more specimens are prepared.

Maternal Size

AGM CHS-5 is a nearly complete skeleton only lacking the tail tip (figure 3A). This specimen is about 1% smaller than AGM I-1 in the length of the second caudal vertebra (10.97 versus 11.16 mm), which we use as the standard for comparing the sizes of incomplete specimens because it has a high exposure rate across the specimens. Its skull is 117.03 mm long, and its skeleton is estimated to be about 100 cm when compensating for the missing tail tip based on the vertebral count and size in CH-628-22, as explained below. We estimated the body and skull lengths of AGM I-1 based on these numbers but they are approximate because no two individuals have strictly identical bone proportions.


Figure 3. Completeness of the two skeletons used in maternal body size estimation.

(A), AGM CHS-5, a nearly complete skeleton that is almost as large as AGM I-1. (B), AGM CH-628-22, a complete skeleton that preserves the tail tip. Large scale bars are 10 cm, and short bars 2 cm.


Skeletal Reconstructions

Each panel of figure 4 was made using the following procedures. First, vertebral column was drawn based on the actual measurements of vertebral size and approximate angle at each vertebral position using a script written for R 3.0.2. Missing measurements were interpolated using a local polynomial curve fit to the available data. The missing tail tip of AGM CHS-5 (figure 3A) was estimated by adding the tail tip vertebra based on AGM CH-628-22 (figure 3B), a slightly smaller specimen with a complete tail, before this polynomial fitting. The tip vertebra was linearly scaled up to match AGM CHS-5, and placed at the correct vertebral position. Other elements were traced from a photograph, scaled, rotated, and transposed to fit the vertebral column in a vector drawing software (CorelDraw). Some ribs were interpolated using the linear morphing function of CorelDraw. Body outlines in black are approximate.


Figure 4. Stylized reconstruction of adult and embryo of Chaohusaurus in comparison to a derived ichthyopterygian.

(A), adult based on AGM I-1 and CHS-5. Rectangle indicates the approximate range preserved in AGM I-1. Colored silhouettes of embryo are placed in approximate positions of embryos 1 and 2, with embryo 3 displaced to avoid overlap with embryo 2. The extent of the maternal tail tip, in gray, is based on AGM-CH-628-22. Scleral ring is based on AGM-CHS-3. (B), embryo based on embryo 2 and neonate 1 of AGM I-1. Elements in gray are missing. (C), the derived ichthyopterygian Stenopterygius with one embryo in birth position and three in body cavity, reconstructed based on SMNS 6293 (Staatliches Museum für Naturkunde, Stüttgart, Germany). Scale bars are 5 cm. See fig. S3 for a high resolution image.



The maternal specimen is incomplete, lacking the skull, anterior trunk, and posterior tail (figure2) because of the way it was collected (see Methods). However, the bones are excellently preserved and well-articulated. Despite the incompleteness, the maternal body size can be estimated from another specimen with almost identical vertebral and pelvic dimensions (AGM CHS-5, figure 3). We estimate the maternal body length to be approximately 100 cm, and the skull length about 12 cm (see Methods).

There are at least three embryos/neonates associated with the maternal skeleton (figure 2), one inside the maternal body cavity (embryo 1), another exiting the pelvic girdle with half of the body still in the maternal body cavity (embryo 2), and the third outside of the maternal body, largely underlying it (neonate 1). The preservation of embryos is exquisite despite the great geologic age. Two of the skulls are articulated, unlike in most fossil embryos [7], [9], [11]. Also, apart from one Jurassic ichthyopterygian specimen (figure 4C), this is the only fossil that captures an articulated embryo in birth position. Embryos 2 and neonate 1 may appear mixed (figure 2) but can be readily delineated from each other because neonate 1 underlies the maternal body whereas embryo 2 is above the right maternal sacral ribs. Also, if the detached tail segment currently assigned to neonate 1 belonged to embryo 2, then the embryo would already be outside the maternal body and there would be no reason for it to be near the maternal pelvic girdle as preserved. Similarly, embryos 1 and 2 occur on different layers, so it is unlikely that the two individuals are confused in figure 2. In addition, based on vertebral size and shape, it is possible to judge that the vertebral columns of the embryos and neonate have caudad orientations except the detached tail segment outside of the maternal body. We estimate the length of an embryo to be about 18 cm, assuming the adult vertebral count (figure 4). The relative embryo to adult size is therefore about 0.18, which is small for an ichthyopterygian but similar to what is known in terrestrial saurians [8], [13].

The skull of embryo 2 is 35 mm long. There are 23 upper and 16 lower teeth preserved in the jaws of embryo 2. When accounting for empty tooth positions, the dental count for the upper jaw is estimated to be about 40 to 45. This is about 10 positions less than the adult condition. All teeth are pointed, although some broken teeth may misleadingly exhibit rounded shape. Adult Chaohusaurus are known for heterodonty, with pointed anterior and rounded posterior teeth [18], [20].


A suite of features supports the inference that two of the small individuals are embryos. First, embryo 1 is completely enclosed inside the maternal body cavity and embryo 2 partially enclosed in the maternal pelvic girdle, eliminating a possibility of preservational superimposition. Second, there is no indication of predation or digestion. The bones are not etched by stomach acid and the skeletons are sufficiently well-articulated despite their terminal position. Third, the large relative skull size and small relative flipper length compared to adult ratios [20] indicate immaturity (figure 4). Fourth, ossification of flipper bones is the least extensive among Chaohusaurus specimens [20], with the entire autopod unossified. The flipper bones appear angular and stout compared to those of the smallest juvenile known [20], again indicating immaturity. Fifth, tooth shape also suggests immaturity of these individuals. It is known among some extant heterodont lizards [21] and Chaohusaurus [20] that the degree of heterodonty is age-related, with younger individuals having progressively isodont (i.e., uniform tooth shape) dentition. Therefore, isodonty seen in this specimen is expected in embryos of Chaohusaurus. Finally, the skull suture pattern of embryo 2 is very similar to that of adults, suggesting that it is conspecific with the adults.

Viviparity in extant reptiles is known only among squamates. Despite the traditional four-step evolutionary model from lecithotrophy to placentotrophy, squamate reproductive strategies are almost bimodally divided between oviparity (egg laying), including cases of egg retention up to limb-bud stage, and viviparity involving functional placentation [2], with few intermediate forms [22]. Therefore, viviparity seems to evolve simultaneously with functional placentation in squamates [23]. Given these observations, it would be reasonable if viviparity in Chaohusaurus involved a degree of placentation. However, this inference cannot be tested directly with fossil evidence because the soft tissue is not preserved.

Embryo 2 is in birth position but this location alone does not necessitate a death during parturition. A similar case for the Jurassic ichthyopterygian Stenopterygius (figure 4C) has been interpreted as postmortem expunging of an embryo, clogging the birth canal, by abdominal gas from decomposition—note that cranially-located embryos were not pushed backed by the gas in the specimen of Stenopterygius [13]. However, in the present specimen, neonate 1 lies outside the maternal body in the present specimen, suggesting that the mother had already given birth to at least one offspring before it died. Placement of embryos 1 and 2 near the pelvic girdle, respectively, suggests that embryos were at least full term. Considering these factors, we conclude that the mother likely died in labor. Given that the rock containing the fossil is marine, parturition most likely occurred underwater.

Both articulated skulls are pointing caudally, and so is the disarticulated skull of neonate 1 (figure 2). We hereafter define directions based on the mother, e.g., caudad means toward the maternal tail tip. It is likely that newborns were expelled headfirst (figure 4A), given the uniform orientation of the embryonic skulls and the lack of room for reorientation of embryos. It is unlikely that all three individuals represent a breech condition. For example, if a possibility of breech is, say, 10%, then chances of having three consecutive breech births is only 0.1%. A similar condition in the basal whale Maiacetus was interpreted as evidence for terrestrial birth [24], although anatomical differences between the two forms prevent a direct comparison. It is generally thought that embryos of aquatic amniotes, including whales, sea cows, and ichthyopterygians, are born tail-first (figure 4C), possibly to avoid suffocation during parturition [9], [25], [26]. However, at least some newborns are expelled headfirst in Yellow-bellied Sea Snake (Pelamis platura) [27], White Whale (Delphinapterus leucas) [28], and the derived ichthyosaurian Stenopterygius [13], although the majority of individuals are born tail-first. These cases may be exceptions but nevertheless establish that headfirst birth in water is possible even in air-breathers. Therefore, the caudad skull orientation of embryonic Chaohusaurus does not necessarily suggest birth on land, especially if this mother died in labor underwater as preservational evidence suggests.

Although a case for terrestrial birth cannot be established in Chaohusaurus, the uniformly caudad skull orientation of its embryos does suggest that viviparity in Ichthyopterygia most likely evolved in their ancestor on land, where caudad embryonic skull orientation during parturition is the norm. The small relative size of embryos, comparable to the mean terrestrial proportions as pointed out earlier, supports this inference. Thus, the craniad orientation of the embryonic skull (figure 4C) is a derived condition within Ichthyopterygia, probably known only in its subclade Ichthyosauria [18]. The fossil record shows that ichthyosaurs as basal as Mixosaurus of the Middle Triassic [11] already had cranially-oriented embryonic skulls. We interpret this secondary change in skull orientation as an aquatic adaptation, whereas viviparity itself is an inherited terrestrial feature that happened to help the clade become obligatorily marine. Therefore, viviparity is an exaptation in ichthyopterygians [29].

The caudad embryonic skull orientation during underwater parturition may have led to high mortality in early marine invaders [7]. If so, the current fossil has a rare preservation of an embryo in birth posture, together with a deceased neonate because of such high mortality. However, this inference remains speculative until additional evidence is found. A similar case was reported for the freshwater reptile Hyphalosaurus [30].

There is no evidence for a marine origin of viviparity in Mesozoic marine reptiles despite the traditional view. Two clades other than Ichthyopterygia have fossil records of viviparity, viz., Sauropterygia [7], [8] and Mosasauroidea [9]. The embryos of the sauropterygian Keichousaurus are preserved with their skulls pointing caudally without a clear sign of vertebral curling [7], as in Chaohusaurus. This condition strongly indicates a terrestrial origin of viviparity in Sauropterygia. It was suggested that birth in Keichousaurus was expedited by its flexible pelvic girdle, resulting from aquatic adaptation [7]. Such an aquatic adaptation may speed up the birth process as suggested but evidence from extant reptiles is currently lacking to support this hypothesis. Also, this factor may not be relevant to those species with many small embryos in a liter because each newborn is small compared to those of a species with a liter size of one for a given maternal size. At least, the flexible girdle is clearly not a mandatory structure for viviparity because most viviparous reptiles are terrestrial [2]. The presence of curled-up embryos in other Triassic sauropterygians, such as Neusticosaurus [31] and Lariosarus [10], suggests that the reproductive strategy of these amphibious [8] marine reptiles may have been variable. Such a variability within a clade is possible given that at least three species of extant lizards have both viviparous and oviparous populations [22]. Embryos of the mosasauroid Carsosaurus are preserved curled-up, with their heads inclined cranially [9]. Their tails are positioned more cranially than their respective skulls, making tail-first birth unlikely. They may have been born curled-up, as in some extant lizards that give birth on land. Mosasauroids are squamates [32], which are known for unusually high abundance of viviparity [2]. The fossil record of viviparity in this group is at least 30 million years older than that for Carsosaurus [33]. Therefore, viviparity in mosasauroids probably was inherited from their land ancestor.

Hyphalosaurus from the Cretaceous of China is another example of viviparous aquatic reptile, although it lived in freshwater [30]. A case is known where two terminal embryos within the maternal body cavity were straightened while the others still remained curled, most likely in their egg sacs [30]. Therefore, its viviparity is similar to that of some living squamates, where birth posture varies [34]. Its egg membrane microstructure is also similar to that of squamates [35]. It is unclear how this example relates to the present case of Chaohusaurus, for which there is no evidence of embryonic body curling at this point—no ichthyopterygian embryo has been found with a curled body posture.

The marine origin of viviparity is also unknown among extant obligate marine amniotes. Viviparity likely evolved only once in mammals [36], so all marine mammals inherited it from their land ancestors. The only extant obligatory marine reptiles are hydrophiine sea snakes. Note that we consider only those animals that feed almost exclusively in the sea as marine animals [37]. The origin of hydrophiine viviparity had been ambiguous [38][40], but a recent molecular phylogenetic study clarified that they are a part of a viviparous clade whose basal members are all terrestrial [41]. Therefore, it is most likely that their viviparity also evolved on land.

Overall, no case is known for the marine origin of viviparity in strictly obligatory marine amniotes through time, whether extinct or extant, based on either phylogenetic bracketing or birth postures in basal forms. A possible reason for this absence is temperature. Studies of extant reptiles suggested that viviparity evolved in cold climates, where thermoregulation through maternal behavior leads to high incubation temperature [1], [42], [43]. Behavioral thermoregulation is expected to be less effective in the sea, where temperature is more stable and has higher minimum values than on land [44]. Thus, amniote viviparity is expected to have higher selective advantage on land than in the sea. Fish viviparity is irrelevant to the present discussion because amniote eggs develop on land [9].

Terrestrial origins of viviparity in Mesozoic marine reptiles may be a departure from the conventional wisdom. However, it agrees well with the general knowledge of viviparity in extant amniotes, as discussed above. The null assumption for viviparity in obligate marine amniotes should be that it evolved in terrestrial ancestors and not in the sea, unless evidence to the contrary is found. The oldest fossil evidence of viviparity in land reptiles is at most 125 million years old [33]. However, this seemingly young age is probably because of preservation bias against small terrestrial vertebrates [45]. Both Ichthyopterygia and Sauropterygia most likely evolved from viviparous land ancestors in the Early Triassic, at least as early as 248 million years ago. Therefore, viviparity may have already been common among terrestrial reptiles during the recovery phase from the end-Permian mass extinction.

Supporting Information

Figure S1.

High resolution version of Fig. 1.



Figure S2.

High Resolution Version of Fig. 2.



Figure S3.

High resolution version of Fig. 4.




We thank Tetsuya Sato for the skillful preparation of the specimen. Chris McGowan and Geerat Vermeij provided suggestions to an earlier version of the manuscript.

Author Contributions

Conceived and designed the experiments: RM DJ AT OR GC. Performed the experiments: RM DJ AT. Analyzed the data: RM DJ AT. Contributed reagents/materials/analysis tools: RM DJ AT GC. Wrote the paper: RM.


  1. 1. Shine R (2005) Life-history evolution in reptiles. Annual Review of Ecology Evolution and Systematics 36: 23–46.
  2. 2. Blackburn DG (2006) Squamate reptiles as model organisms for the evolution of viviparity. Herpetological Monographs: 131–146.
  3. 3. Long JA, Trinajstic K, Young GC, Senden T (2008) Live birth in the Devonian period. Nature 453: 650–U656.
  4. 4. Gradstein FM, Ogg JG, Schmitz MD, Ogg GM (2012) The Geologic Time Scale 2012. Oxford, UK: Elsevier. 1144 p.
  5. 5. Pineiro G, Ferigolo J, Meneghel M, Laurin M (2012) The oldest known amniotic embryos suggest viviparity in mesosaurs. Historical Biology 24: 620–630.
  6. 6. Rafferty AR, Evans RG, Scheelings TF, Reina RD (2013) Limited Oxygen Availability In Utero May Constrain the Evolution of Live Birth in Reptiles. American Naturalist 181: 245–253.
  7. 7. Cheng YN, Wu XC, Ji Q (2004) Triassic marine reptiles gave birth to live young. Nature 432: 383–386.
  8. 8. O'Keefe FR, Chiappe LM (2011) Viviparity and K-Selected Life History in a Mesozoic Marine Plesiosaur (Reptilia, Sauropterygia). Science 333: 870–873.
  9. 9. Caldwell MW, Lee MSY (2001) Live birth in Cretaceous marine lizards (mosasauroids). Proceedings of the Royal Society B-Biological Sciences 268: 2397–2401.
  10. 10. Renesto S, Lombardo C, Tintori A, Danini G (2003) Nothosaurid embryos from the Middle Triassic of northern Italy: An insight into the viviparity of nothosaurs? Journal of Vertebrate Paleontology 23: 957–960.
  11. 11. Brinkmann W (1996) Ein Mixosaurier (Reptilia, Ichthyosauria) mit Embryonen aus der Grenzbitumenzone (Mitteltrias) des Monte San Giorgio (Schweiz, Kanton Tessin). Eclogae Geologicae Helvetiae 89: 1321–1344.
  12. 12. Dal Sasso C, Pinna G (1996) Besanosaurus leptorhynchus n. gen n. sp., a new shastasaurid ichhyosaur from the Middle Triassic of Besano (Lombardy, N. Italy). Paleontologia Lombarda, Nuevo Serie 4: 3–23.
  13. 13. Boettcher R (1990) New Information on the Reproductive Biology of Ichthyosaurs (Reptilia). Stuttgarter Beitraege zur Naturkunde Serie B (Geologie und Palaeontologie): 1–51.
  14. 14. Motani R (2002) Scaling effects in caudal fin propulsion and the speed of ichthyosaurs. Nature (London) 415: 309–312.
  15. 15. Motani R, Rothschild BM, Wahl W (1999) Large eyeballs in diving ichthyosaurs - The huge eyes of these extinct reptiles may have been useful deep in the ocean. Nature 402: 747–747.
  16. 16. Maxwell EE, Caldwell MW (2003) First record of live birth in Cretaceous ichthyosaurs: closing an 80 million year gap. Proceedings of the Royal Society B-Biological Sciences 270: S104–S107.
  17. 17. Deeming DC, Halstead LB, Manabe M, Unwin DM (1993) An ichthyosaur embryo from the Lower Lias (Jurassic: Hettangian) of Somerset, England, with comments on the reproductive biology of ichthyosaurs. Modern Geology 18: 423–442.
  18. 18. McGowan C, Motani R (2003) Ichthyopterygia; Sues H-D, editor. München: Verlag Dr. Friedrich Pfeil. 175 p.
  19. 19. Stone R (2010) PALEONTOLOGY Excavation Yields Tantalizing Hints Of Earliest Marine Reptiles. Science 330: 1164–1165.
  20. 20. Motani R, You H (1998) Taxonomy and limb ontogeny of Chaohusaurus geishanensis (Ichthyosauria), with a note on the allometric equation. Journal of Vertebrate Paleontology 18: 533–540.
  21. 21. Edmund AG (1969) Dentition. In: Gans C, Bellairs AdA, Parsons TS, editors. Biology of the Reptilia Morphology A. London: Academic Press. pp. 117–200.
  22. 22. Smith SA, Shine R (1997) Intraspecific variation in reproductive mode within the scincid lizard Saiphos equalis. Australian Journal of Zoology 45: 435–445.
  23. 23. Blackburn DG (1995) Saltationist and Punctuated Equilibrium-Models for the Evolution of Viviparity and Placentation. Journal of Theoretical Biology 174: 199–216.
  24. 24. Gingerich PD, ul-Haq M, von Koenigswald W, Sanders WJ, Smith BH, et al.. (2009) New Protocetid Whale from the Middle Eocene of Pakistan: Birth on Land, Precocial Development, and Sexual Dimorphism. PLoS One 4: Article No.: e4366.
  25. 25. McBride AF, Kritzler H (1951) Observations on pregnancy. parturition, and postnatal behavior in the bottlenose dolphin. Jour Mammal 32: 251–266.
  26. 26. Marsh H, Heinsohn GE, Marsh LM (1984) Breeding Cycle Life History and Population Dynamics of the Dugong Dugong-dugon (Sirenia: Dugongidae). Australian Journal of Zoology 32: 767–788.
  27. 27. Vallarino O, Weldon PJ (1996) Reproduction in the yellow-bellied sea snake (Pelamis platurus) from Panama: Field and laboratory observations. Zoo Biology 15: 309–314.
  28. 28. Robeck TR, Monfort SL, Calle PP, Dunn JL, Jensen E, et al. (2005) Reproduction, growth and development in captive beluga (Delphinapterus leucas). Zoo Biology 24: 29–49.
  29. 29. Gould SJ, Vrba ES (1982) Exaptation - a Missing Term in the Science of Form. Paleobiology 8: 4–15.
  30. 30. Ji Q, Wu XC, Cheng YN (2010) Cretaceous choristoderan reptiles gave birth to live young. Naturwissenschaften 97: 423–428.
  31. 31. Sander PM (1988) A Fossil Reptile Embryo from the Middle Triassic of the Alps. Science 239: 780–783.
  32. 32. Bell GL, Polcyn MJ (2005) Dallasaurus turneri, a new primitive mosasauroid from the Middle Turonian of Texas and comments on the phylogeny of Mosasauridae (Squamata). Netherlands Journal of Geosciences-Geologie En Mijnbouw 84: 177–194.
  33. 33. Wang Y, Evans SE (2011) A gravid lizard from the Cretaceous of China and the early history of squamate viviparity. Naturwissenschaften 98: 739–743.
  34. 34. Hunsaker DON (1959) Birth and Utter sizes of the blue spiney lizard Sceloporus cyanogenys. Copeia 1959: 260–261.
  35. 35. Hou LH, Li PP, Ksepka DT, Gao KQ, Norell MA (2010) Implications of flexible-shelled eggs in a Cretaceous choristoderan reptile. Proceedings of the Royal Society B-Biological Sciences 277: 1235–1239.
  36. 36. Renfree MB, Suzuki S, Kaneko-Ishino T (2013) The origin and evolution of genomic imprinting and viviparity in mammals. Philosophical Transactions of the Royal Society B-Biological Sciences 368.
  37. 37. Motani R (2009) The evolution of marine reptiles. Evolution: Education and Outreach 2: 224–235.
  38. 38. Shine R (1985) The Evolution of Viviparity in Reptiles an Ecological Analysis. In: Gans C, Billett F, editors. Biology of the Reptilia. New York: John Wiley and Sons. pp. 605–694.
  39. 39. Blackburn DG (1999) Are viviparity and egg-guarding evolutionarily labile in squamates? Herpetologica 55: 556–573.
  40. 40. Blackburn DG (1985) Evolutionary Origins of Viviparity in the Reptilia Ii. Serpentes Amphisbaenia and Ichthyosauria. Amphibia-Reptilia 6: 259–291.
  41. 41. Sanders KL, Lee MSY, Leys R, Foster R, Keogh JS (2008) Molecular phylogeny and divergence dates for Australasian elapids and sea snakes (hydrophiinae): evidence from seven genes for rapid evolutionary radiations. Journal of Evolutionary Biology 21: 682–695.
  42. 42. Rodriguez-Diaz T, Brana F (2012) Altitudinal variation in egg retention and rates of embryonic development in oviparous Zootoca vivipara fits predictions from the cold-climate model on the evolution of viviparity. Journal of Evolutionary Biology 25: 1877–1887.
  43. 43. Bleu J, Heulin B, Haussy C, Meylan S, Massot M (2012) Experimental evidence of early costs of reproduction in conspecific viviparous and oviparous lizards. Journal of Evolutionary Biology 25: 1264–1274.
  44. 44. Sunday JM, Bates AE, Dulvy NK (2011) Global analysis of thermal tolerance and latitude in ectotherms. Proceedings of the Royal Society B-Biological Sciences 278: 1823–1830.
  45. 45. Brown CM, Evans DC, Campione NE, O'Brien LJ, Eberth DA (2013) Evidence for taphonomic size bias in the Dinosaur Park Formation (Campanian, Alberta), a model Mesozoic terrestrial alluvial-paralic system. Palaeogeography Palaeoclimatology Palaeoecology 372: 108–122.