Bibliography S


Phylogeny

Pathology

Location

Turtles
  
Toxochelys? (LACM 50974 Campanian)

Serrated bite marks

Humerus

Desmatochelys lowii (KUVP 32401 Turonian)

Parallel serrated cuts

Humerus

KUVP 32405 Turonian

Cut marks, occ serrated

Humerus

Protostega gigas (ALAM PV985.10.2 Campanian)

Bite marks

Humerus

Bothremys barberi (CSUK 90–17–3 Schmidt 1940)

Scrape marks

Carapace

Mosasaurs
  
Platecarpus ictericus (LACM 131156 Campanian)

Cuts, most with serration

Ribs

Platecarpus sp. (KUVP 86656 Senonian)

Serrated cut marks

Pubis and ischium

Tylosaurus proriger (FHSM VP-3 Senonian)

Bite marks with serration

Mandible

Mosasauridae (FHSM VP-2156 Senonian)

Serrated cut marks

Ilium

KUVP 1117 Senonian

Bite marks, some serrated

Radius or ulna

DNMH no # Campanian

Bite marks

Vertebra

Plesiosauria, Polycotylidae
  
Dolichorhynchops sp. (FHSM VP 12059 Turonian)

Serrated bite marks

Coracoid

Trinacromerum willistoni (KUVP 5070 Turonian)

Bite marks

Pubis

Plesiosauria, Pliosauridae
  
Brachauchenius lucasi (FHSM no # Turonian)

Serrated tooth marks

Rib
 
With embedded
  
Squalicorax tooth
 


Schwind JL. 1942. Spontaneous twinning in the Amphibia. – American Journal of Anatomy 71:117–151.

Congenital – Dicephalic Rana sylvatica and several cases of anterior back and head duplication and a supernumerary limb.


Twinning in 27 Rana sylvatica from Alpine, New Jersey.

Scott H. 1927. Report on deaths occurring in the Society’s Gardens during the year 1926. Proceedings of the Zoological Society London 1927:173–198.

Infection – Tuberculosis in Aesculapian snake, rough-eyed Cayman, and Mexican black iguana, but no comment on bone disease.


Metabolic – Rickets presenting as soft bones in Hilaire’s terrapin.

Scott AF. 1982. Eumeces fasciatus (five-lined skink) morphology. Herpetological Review 13(2):46.

Trauma – Bifid-tailed five-lined skink Eumeces fasciatus, citing bifid and trifid tailed lizards (Smith 1946; Banta 1963; Couch 1969; Goin and Goin 1971; Clark 1973).

Scott PW. 1992. Nutritional diseases. Pp. 138–152. in Beynon P, Lawton MP, Cooper JE (eds.), Manual of Reptiles. Cheltenham: British Small Animal Veterinary Association.

Metabolic – Nutritional osteodystrophy in Iguana iguana.


Lumpy shell with pyramiding in turtles from calcium deficiency/rickets.

Sealander JA. 1944. A teratological specimen of the tiger salamander. Copeia 1944:63.

Congenital – Tiger salamander Ambystoma tigrinum tigrinum with supernumerary forearm with seven toes.

Seba A. 1734. Locupletissimi rerum naturalium thesauri accurate description, et iconibus artificiosissimis expression, per universam physics historiam. [Cabinet of Natural Curiosities accurate description and artificial images of universal physical history]. Amstelaedami: Janssonio-Waesbergios & J. Wetstenium. [Latin]

Other – Drawing of snake with peculiar constricted distal tail (Vol 2, plate 30).


Pseudopathology – noted general problem existed of accuracy errors (e.g., limbs incorrectly positioned).


Hydra – Seven-headed serpent representation with two forefeet and a long tail, which allegedly belong to Count von Königsmark. The mouths were open and lined with “lion’s teeth” including canines. Also noted a similar report by Conrad Gesner and by Aldovandas and cites “page 91 of 8th book on subterranean animals by Athanasius Kircher.”


Myhtology – Seven-headed serpent representation with two forefeet and a long tail, which allegedly belong to Count von Königsmark. The mouths were open and lined with “lion’s teeth” including canines. Also noted a similar report by Conrad Gesner and by Aldovandas and cites “page 91 of 8th book on subterranean animals by Athanasius Kircher.”

Seeley HG. 1898. On the skull of Mochlorhinus platyceps, from Bethulie, Orange Free State, preserved in the Albany Museum, Grahamstown. Annals and Magazine of natural History (7) 1:164–176.

Congenital – Unpaired, median bone, “praeparietale,” between parietals and frontals in dicynodont therapsid (mammal-like reptiles), Lystrosaurus (his Mochlorhinus) platyceps.


Fossil – Unpaired, median bone, “praeparietale,” between parietals and frontals in dicynodont therapsid (mammal-like reptiles), Lystrosaurus (his Mochlorhinus) platyceps.

Seeley HG. 1892 The mesosauri of South Africa. Quarterly Journal of the Geological Society (of London) 48:586–604.

Congenital – Illustration in Fig. 5 of two Mesosaurus clavicles fused into a single transverse bar, but not discussed in text.


Fossil – Illustration in Fig. 5 of two Mesosaurus clavicles fused into a single transverse bar, but not discussed in text.

Seidel MR. 1979. The Osteoderms of the American alligator and their functional significance. Herpetologica 35:375–380.

Metabolic – Osteoderm role in Alligator mississippiensis in heat transmission and release because of vasculature.

Seligmann H. 1997. Tail injury alters activity patterns in Podarcis muralis (Reptilia: Lacertidae). Israel Journal of Zoology 44:87.

Trauma – Podarcis muralis with regenerated tails moved less often and spent less time in vertical movement.

Seligmann H. 1998. Evidence that minor directional asymmetry is functional. Journal of Zoology 245:205–208.

Congenital – Significant correlation between minimal directional asymmetry and injury, but not with specific side.

Seligmann H. 2000. Evolution and ecology of developmental processes and of the resulting morphology: Directional asymmetry in hindlimbs of Agamidae and Lacertidae (Reptilia: Lacertilia). Biological Journal of the Linnean Society 69:461–481.

Trauma – Notes fourth toe most commonly injured in Agamidae and Lacertidae.


Injuries related to intraspecific combats and from unsuccessful predation attempts.


Correlation between minimal directional asymmetry and injury was stronger in Agamidae than Lacertidae, possibly related to different foraging patterns.

Seligmann H. 2001. Microevolution of proneness to tail loss in lizards. Ph.D. Thesis. Jerusalem: Hebrew University of Jerusalem.

Trauma – Frequency of regeneration correlates with sex in geckos (Werner 1968), geography in teids (Schall and Pianka 1980), altitude in iguanids (Brown and Ruby 1977) and tail shedding with temperature in Gehyra (Bustard 1968) and Stenodactylus (Werner 1968).


Tail loss reduces bipedal running speed in Dipsosaurus (Pond 1978), doubled speed in Phyllodactylus (Daniels 1983) and was associated with increased survival in Uta stansburiana (Niewiarowsky et al. 1997). Males have higher resistance to tail breakage (Fox et al. 1998).


10% of Thamnophis sirtalis fitchi had injured tails, possibly from cattle trampling (Jayne and Bennett 1989) with negative correlation between speed and extent of tail amputation.

Seligmann H, Krishnan NM. 2006. Mitochondrial replication origin stability and propensity of adjacent tRNA genes to form putative replication origins increase developmental stability in lizards. Journal of Experimental Zoology (Molecular Development and Evolution) 306B:433–449.

Congenital – Positive association between low genetic variability and developmental anomalies (Soulé 1979), more in Anguidae than Amphisbaenidae (Gautschi et al. 2002). Increased frequency of scale anomalies and loss of genetic variation in serially bottlenecked populations of the dice snake Natrix tessellate.

Seligmann H, Beiles A, Werner YL. 1996a. Tail loss frequencies of lizards and predator specialization. Proceedings of the Sixth International Conference of the Israeli Society for Ecology and Environmental Quality Sciences. In Y Steinberger, ed. Preservation of Our World in the Wake of Change. Jerusalem: ISEEQS Pub. VI A/B:520–522.

Trauma – Lizard tail loss is more common when there is high pressure by predators for which lizards are a small percentage of the diet.

Seligmann H, Beiles A, Werner YL. 1996b. Morphotypes related to tail loss in lizards. Proceedings of the Sixth International Conference of the Israeli Society for Ecology and Environmental Quality Sciences. In Y Steinberger, ed. Preservation of Our World in the Wake of Change. Jerusalem: ISEEQS Pub. VI A/B:44–47.

Trauma – Tail loss causes low social hierarchy (Fox and Baxter 1982) and decreased clutch size (Ballinger and Tinkle 1979; Dial and Fitzpatrick 1981).


Link between tail loss frequency and predation depends on predator specialization; predators more often take atypical animals.


Longer limbs correlated with retention of original tail in Acanthodactylus pardalis.

Seligmann H, Beiles A, Werner YL. 2003. Avoiding injury and surviving injury: Two coexisting evolutionary strategies in lizards. Biological Journal of the Linnean Society 78:307–324.

Trauma – Proneness to tail shedding is hereditary, greater in lizards from predator-dense mainland than insular localities (Pérez-Mellado et al. 1997).


Regeneration is greater among paedotypic individuals.


Frequency of regeneration correlates with sex in geckos (Werner 1968), geography in teids (Schall and Pianka 1980), altitude in iguanids (Brown and Ruby 1977), and tail shedding with temperature in Gehyra (Bustard 1968) and Stenodactylus (Werner 1968).


Tail loss reduces perch height in Anolis (Ballinger 1973), bipedal running speed in Dipsosaurus (Pond 1978), Cnemidophorus (Ballinger et al. 1979), and Cophosaurus (Punzo 1982), climbing speed in Podarcis muralis (Brown et al. 1995), percent of time moving in Lacerta monticola (Martin and Salvador 1997) and Podarcis muralis (Seligmann 1997), success of escape from predators in Scincella (Dial and Fitzpatrick 1984), growth in Sceloporus (Ballinger and Tinkle 1979), and female reproductive investment (related to tail loss and regeneration) in Coleonyx (Dial and Fitzpatrick 1981).


Tail loss in Lacerta monticola results in shift in habitat use (Martin and Salvador 1992), decrease in home range and female access in Psammodromus algirus (Salvador et al. 1995), and decrease in social status in Uta stansburiana (Fox and Rostker 1982; Fox et al. 1990).


Loss of tail in Scincella is compensated for by cryptic behavior (Formanowicz et al. 1990).


Advantage is given by the clubbed regenerated tails in male Agama agama (Schall et al. 1989).


Regenerated tail mimics head shape in Hemitheoconyx caudicinctus (Werner 1972), fooling predators.

Seligmann H, Moravec J, Werner YL. 2008. Morphological, functional and evolutionary aspects of tail autotomy and regeneration in the ‘living fossil’ Sphenodon (Reptilia: Rhynchocephalia). Biological Journal of the Linnean Society 93:721–743.

Trauma – Autotomy, usually with regeneration, occurs in lizards, snakes, and amphisbaenians. Left-handed lizards are accident-prone (injured digits more frequently), lose tail more frequently, suggests greater fluctuating asymmetry in tail losers. Tail retainers are more frequently right-sided dominant.


Sphenodon has 36–29 caudal vertebrae – number uncertain, as intact tails difficult to find – and may live 100 years (Dawbin 1982). Goniourosaurus kuroiwae may also be long lived, as 91% have regenerated tails (Werner et al. 2006). Percentage of intact tails in Sphenodon decreases 1.14% in juveniles and 0.86% in adults per year.


Tail breakage (especially from intraspecific, intrasexual bites) was usually intravertebral in tuatara Sphenodon. Tail losers were more left-sided dominant. Only two lizard taxa exceeded regeneration rate of Sphenodon: Arabian Asaccus (“Phylodactylus”) and Agama bibronii (Arnold 1984).


Regeneration occurs not from end of stump, but from ablation of approximately the posterior half of terminal half-vertebra – from caudal 10 to 27 – and regenerates as a rod, rather than a tube, and is gender-neutral.


Occasional bifurcated tail in Sphenodon.


Homeosaurus is a Jurassic sphenoid with autotomy (Barbour and Stetson 1929).


Autotomy is frequent, but with regeneration in Amphisbaenia (Gans 1978). The only snake with regeneration was Amphiesma stolatum (Sharma 1980).


Terminal stumps of Zootoca (“Lacerta”) vivipara have terminal vertebral units shorter than a half-vertebra (Bellairs and Bryant 1985), as in Takydromus septentrionalis (Boring et al. 1948), in contrast to Laudakia stellio which retains ¾ of terminal vertebra.


Tail regeneration in some crocodiles (Dathe 1960).

Seligmann H, Beiles A, Werner YL. 2003. More injuries in left-footed lizards. Journal of Zoology (London) 260:129–144.

Congenital – Lacertidae asymmetries associate with tail state. Right side is dominant in toads. Most species are right dominant: Agamidae 15/21, Anguidae 4/12, Gekkonidae 27/46, Gymnophthalmidae 9/12, Iguanidae 4/9, Lacertidae 34/48, Scincidae 22/37, Teidae 3/5, Varanus griseus, Lepidophyma flavimaculatum, and Sphenodon punctatus. Right dominance was significant in Sphenodon, Anguidae Mesaspis gadovii, Gekkonidae Stenodactylus sthenodactylus, Gekko swinhonis, Lacertidae Acanthodactylus boskianus, A. schmidti, Eremias argus, Lacerta laevis, Meroles anchietae, Mesalina olivieri, and Sphenodontidae Sphenodon punctatus. Left dominance was found in Calotes versicolor and Ptyodactylus guttatus.


Trauma – Lacertidae asymmetries associate with tail state. Right side is dominant in toads. Agamidae have more injuries on the right hind limb, “presumably reflecting more use of that side.” (p. 130). Injured lizards were more frequently left dominant: Agamidae 16/21, Gekkonidae 31/46, Gymnophthalmidae 5/12, Iguanidae 4/9, Lacertidae 25/48, Scincidae 17/37, Teidae 3/5, Varanus and Sphenodon. Gymnophthalmus underwoodi, Crotaphytus collaris, and Sphenops sepsoides (Scincidae) were significantly more right-sided.


Injured terrestrial Rhoptropus afer and Tropiocolotes nattereri were left- dominant, in contrast with tree-climbing relatives.


Rate of injured increased with body size, apparently as a corollary of age in left dominant Ptyodactylus guttatus and Laudakia stellio, but not with Acanthodactylus beershebensis or Mesalina guttulata.

Semlitsch RD, Moran GB, Shoemaker CA. 1981. Life history notes. Caudata, Ambystoma tadpoideum (mole salamander). Morphology. Herpetological Review 12:69.

Congenital – Polydactyly in mole salamander Ambystoma tadpoideum.

Sequeira F, Goncalves H, Menses C, Mouta-Faria M. 1999. Morphological abnormalities in a population of Chioglossa lusitanica. Boletín de la Asociación Herpetológica Española 10: 35–36.

Congenital – Forelimb polymelia in one, polydactyly in six, ectodactyly in 13 in one of 1738 Chioglossa lusitanica.


Trauma – Bifid tail in one of 1738 Chioglossa lusitanica.

Sessions SK. 1996–1997. Evidence that trematodes cause deformities, including extra limbs, in amphibians. In Anon. NAAMP III. The North American Amphibian Monitoring Program Third Annual Meeting. 12 unnumbered pages; Patuxent, MD.: US Geological Survey, Biological Resources Division.

Environmental – Parasitic flatworm Manodistomum syntomentera form cysts in Pacific tree frogs Hyla regilla and long-toed salamanders Ambystoma macrodactylum. 72% of young had missing limbs, ectopic limbs, polydactyly. 40% of 4148 larval and newly metamorphosized and 5% of 1778 adult salamanders had deformities.

Sessions SK, Ruth SB. 1990. Explanation for naturally occurring supernumerary limbs in amphibians. Journal of Experimental Zoology 254:38–47.

Environmental – Trematode (Ribeiroia ondatrae) cyst infestation induced deformities in Pacific Tree frogs (Hyla regilla). Of 280, 140 had extra limbs, 55 grossly distorted, 13 shortened, nine with extra pelvis, four with missing limb. Among 6000 Ambystoma macrodactylum, predominantly hind limb involvement, with polydactyly in 230, forked digits in 12, syndactyly in 17, supernumerary limbs in 30, ectopic hand/ft in 70, short limbs in four, and missing limbs in three.

Sessions SK, Franssen RA, Horner VL. 1999. Morphological clues from multilegged frogs: are retinoids to blame? Science 284:800–802.

Congenital – Multilegged cascade frog Rana cascadae from Oregon, wood frog Rana sylvatica and green frog Rana clamitans from New York and leopard frog Rana pipiens from Arizona. Bone triangles also reported.

Seymour RS. 1974. How sea snakes may avoid the bends. Nature 250:489–490.

Vascular – skin permeability to the effect of venous shunting in Pelamis platurus and Pseudemys scripta.

Seymour RS. 1978. Gas tensions and blood distribution in sea snakes at surface pressure and at simulated depth. Physiological Zoology 51:388–407.

Vascular – Twenty-eight percent of shallow diving Laticauda colubrina sea snake cardiac output bypasses lung via intrapulmonary and intraventricular shunting, compared with 70% in deep diving Hydrophis belcheri, where blood nitrogen levels are independent of depth. This offers protection from decompression-induced nitrogen bubble formation.

Shacham B. 2005. Tail injury linked to morphological asymmetry in a polymorphic snake. Israel Journal of Zoology 51:77–78.

Congenital – Higher escape frequency in rear-stripped Psammophis schokari suggests that symmetry correlates with escape ability.

Shaffer HB. 1978. Relative predation pressure on salamanders (Caudata, Plethodontidae) along an altitudinal transect in Guatemala. Copeia 1978:268–272.

Trauma – Male lizards have more tail loss (Pianka 1967; Vitt et al. 1974).


Female neotropical salamanders have more tail loss than males:






















































Species

% Male tail loss

% Female tail loss

Pseudoeurycea rex

3

5

Bolitoglossa rostrata

3

11

Pseudoeurycea goebeli

5

9

Bolitoglossa resplendens

10

16

Pseudoeurycea brunnata

2

5

Chiropterotriton bromeliacia

9

30

Bolitoglossa flavimembris

4

8

Bolitoglossa engelhardti

4

6

Bolitoglossa franklini

17

23

Bolitoglossa occidentalis

18

16

Shapiro G. 2003. At Mager & Gougelman, the Eyes Have It. The New York Sun 5 March 2003:1.

Congenital – Dicephalic turtle.

Sharma BD. 1980. A rare case autotomy seen in Amphiesma stolatum (Linn., Serpentes: Colubridae. Snake 12:60).

Trauma – Two Amphiesma stolatum with missing tails.

Shaver DJ, Chaney AH. 1989. An analysis of unhatched Kemp’s Ridley sea turtle eggs. In: CW Caillouet, AM Landry (eds.). Proceedings of the First Symposium on Kemp’s Ridley Sea Turtle Biology, Conservation and Management, p. 82–89. Galveston.

Congenital – 8.3% of 1333 Lepidochelys kempi embryos that could be staged of the 4165 eggs were deformed: jaw, eyes, carapace, flippers, head, snout. The frequencies varied from 14% in 1980, 27% in 1982, 3% in 1983, 15% in 1984, 11% in 1985, 18% in 1986, and 12% in 1987. Those from 1980 had more jaw deformities, compared to flipper in 1985.


They also stated that 0.5% of 8395 hatching in the 1982–1987 “class” had deformities, including jaws, eyes, flipper, neck, and plastron Jaw pathologies – 2.3% Upper or lower missing, abnormally long, short, or split.


Eye pathologies – 1.8% – Cyclopia or abnormal size.


Flipper pathology – 1.7% – Missing, short, narrow, wide, polydactyly, or clawless.


Head pathology – 1.6% – Absent, dicephalic, enlarged, lumped.


Snout pathology – 0.6% – Abnormally long or short.


Carapace pathology – 1.8% – Saddleback, indentaition, curved, contorted, small, narrowed, or missing posterior component.


Plastron pathology – 0.2% – Incomplete.

Shaw CE. 1954. Captive-bred Cuban iguanas Cyclura macleayi. Herpetologica 10: 73–8.

Congenital – Twin Cuban iguanas Cyclura macleayi.

Shaw CE. 1955 Dudley’s second birthday. Zoonoz 28(12):11.

Congenital – Dicephalic California king snake – second birthday.

Shaw CE. 1956. Dudley-Duplex did it again! Zoonoz 29(12):12.

Congenital – Dicephalic California king snake – third birthday.

Shaw CE. 1958. Dudley Duplex …. Devours two mice at the same time. Zoonoz 31(11):9.

Congenital – Dicephalic king snake devours two mice at the same time.

Shaw CE. 1959. Double trouble. Zoonoz 32(11):10–11.

Congenital – Dicephalic California king snake – sixth birthday.

Shaw CE. 1963. Notes on the eggs, incubation and young of some African reptiles. British Journal of Herpetology 3:63–70.

Congenital – Varanus e. albigularis with skewed upper jaw and longer lower jaw.

Shaw CE. 1968. Double trouble again. Zoonoz 41(4):4–6.

Congenital – Dicephalic California king snake Lampropeltis getula californiae.

Shaw CE. 1971. A two-headed tale. Zoonooz 44:4–7.

Congenital – four dicephalic California king snakes donated in 17 years to San Diego zoo.

Shaw CE, Campbell S. 1974. Snakes of the American West. 330 pp.; New York: Alfred A. Knopf inc.

Congenital – Dicephalic king snake survives 6 years.

Sheldon MA, Bell GL Jr. 1999. Paedomorphosis in Mosasauroidea (Squamata): Evidence from fossil bone microstructure. Paludicola 2:190–205.

Congenital – Related paedomorphism to giantism.


Fossil – Related paedomorphism to giantism in mosasauroidea.

Sheppard L, Bellairs A. 1972. The mechanism of autotomy in Lacerta. British Journal of Herpetology 4:276–286.

Trauma – Autotomy in Lacerta dugesii.

Sherman E, Tock K, Clarke C. 2009. Fluctuating asymmetry in Ichthyophonus-sp. Infected newts, Notophthalmus viridescens, from Vermont. Applied Herpetology 6:369–378.

Infection – Increased leg length asymmetry in Notophthalmus viridescens caused by Ichthyophonus infestation.


Environmental – Increased leg length asymmetry in Notophthalmus viridescens caused by Ichthyophonus infestation.

Shilton CM, Brown GP, Shine R, Benedict S. 2008. Spinal arthropathy associated with Ochrobactrum anthropi in free-ranging cane toads (Chaunus [Bufo] marinus) in Australia. Veterinary Pathology 45(1):85–94.

Neuropathic – Spinal changes in 10% of free-ranging cane toads (Chaunus [Bufo] marinus) in Australia. Joint spaces were “indistinct or absent with varying degrees of smooth, moderately firm to rugose bony swelling.” Partial or complete loss of joint space was associated with woven bone and irregular hyaline cartilage islands often bridging adjacent vertebrae. Fifteen lesions were associated with inflammation (dense aggregates of degenerated and necrotic macrophages, some heterophils and neutrophils, necrotic bone and cartilage fragments, with articular cartilage fissure or erosion) while nine fusions manifested none.


Vertebral – Spinal pathology in amphibians has been previously rare and limited to scoliosis (Bacon et al. 2006; Ouellet 2000; Speare 1990).


Spinal changes in 10% of free-ranging cane toads (Chaunus [Bufo] marinus) in Australia. Joint spaces (not disc spaces, which are not found in Bufo) were “indistinct or absent with varying degrees of smooth, moderately firm to rugose bony swelling.” Partial or complete loss of joint space was associated with woven bone and irregular hyaline cartilage islands often bridging adjacent vertebrae. Fifteen lesions were associated with inflammation (dense aggregates of degenerated and necrotic macrophages, some heterophils and neutrophils, necrotic bone and cartilage fragments, with articular cartilage fissure or erosion) while nine fusions manifested none. Some of the toads also had granulomatous gastritis or granulomatous hepatitis or granulomatous cystitis. Culture of six of nine intervertebral spaces revealed Ochrobactrum anthropi (formerly known as Achromobacter and closely related to Brucella).


Notes also the controversial spinal arthropathy of snakes attributed to Salmonella.

Shimada K. 1997. Paleoecological relationships of the Late cretaceous lamniform shark, Cretoxyrhina mantelli (Agassiz). Journal of Paleontology 71:926–933.

Trauma – Review of previously published evidence of shark predation and scavenging, offering opinion on species of shark involved in the attack reported by Rothschild and Martin (1993).

Shimada K, Hooks GE III. 2004. Shark-bitten protostegid turtles from the Upper Cretaceous Mooreville Formation of Alabama. Journal of Paleontology 78:205–210.

Trauma – Protostega gigas FMNH P27452 and FMNH PR58 from the Mooreville Chalk (Upper Santonian to Lower Campanian) in Greene County, Alabama have tooth marks, and FMNH P27452 had five embedded teeth of the Late Cretaceous shark Cretoxyrhina mantelli.


Fossil – Protostega gigas FMNH P27452 and FMNH PR58 from the Mooreville Chalk (Upper Santonian to Lower Campanian), in Greene County, Alabama have tooth marks and FMNH P27452 had five embedded teeth of the Late Cretaceous shark Cretoxyrhina mantelli.

Shimada K, Parris DC. 2007. A long-snouted Late Cretaceous crocodyliform, Terminonaris cf. T. browni, from the Carlile Shale (Turonian) of Kansas. Transactions of the Kansas Academy of Science 110:107–115.

Congenital – Terminonaris cf. T. browni FHSM VP-4387 with fused nasals and maxillae, contrasted with the holotype, which exhibits sutures. They suggested that it could represent variation.


Fossil – Terminonaris cf. T. browni FHSM VP-4387 with fused nasals and maxillae, contrasted with the holotype, which exhibits sutures. They suggested that it could represent variation.

Shimada K, Tsuihiji T, Sato T, Hasegawa Y. 2010. A remarkable case of a shark-bitten plesiosaur. Journal of Vertebrate Paleontology 30:592–597.

Trauma – Elasmosaurid plesiosaur Futabasaurus suzukii from the Upper Cretaceous of central Japan with broken lamniform shark Cretalamna (= Cretolamna) appendiculata teeth in humerus and three vertebrae.


Fossil – Elasmosaurid plesiosaur Futabasaurus suzukii from the Upper Cretaceous of central Japan with broken lamniform shark Cretalamna (= Cretolamna) appendiculata teeth in humerus and three vertebrae

Shine R, Langkilde T, Wall M, Mason RT. 2005. The fitness correlates of scalation asymmetry in garter snakes Thamnophis sirtalis parietalis. Functional Ecology 19: 306–314.

Congenital – 16% of viviparous red-sided garter snakes Thamnophis sirtalis parietalis have different number of ribs on either side of body, related to suboptimal maternal thermoregulation during pregnancy. Asymmetric males mated less successfully than symmetric males. They noted that gravid viviparous snake and lizard females maintain higher and less variable body temperatures than non-gravid. Females more often had asymmetric ventral scale patterns.

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Aug 6, 2016 | Posted by in INTERNAL MEDICINE | Comments Off on Bibliography S

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