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1.
J Morphol ; 285(9): e21768, 2024 Sep.
Article in English | MEDLINE | ID: mdl-39223904

ABSTRACT

The problem of the origin of the bony shell in turtles has a two-century history and still has not lost its relevance. First, this concerns the issues of the homology, the sources of formation and the ratio of bones of different nature, that is, thecal and epithecal, in particular. This article analyzes various views on the nature of the shell elements, and proposes their typification, based on modern data on developmental biology. It is proposed that the defining characteristic of the types of shell ossifications is not the level of their anlage in the dermis (thecality or epithecality), but, first of all, the primary sources of their formation: (1) neural crest (nuchal and plastral plates); (2) vertebral and rib periosteum (neural and costal plates); and (3) dermal mesenchyme (peripheral, suprapygal and pygal plates, as well as epithecal elements). In addition, there is complete correspondence between these types of ossifications and the sequence of their appearance in the turtle ontogenesis. The data show fundamental coincidence of the modifications of the ontogenetic development and evolutionary formation of the shell ossifications and are in agreement with a stepwise model for the origin of the turtle body plan. Particular attention is paid to the origin of the epithecal elements of the turtle shell, which correspond to the additional or supernumerary ossifications and seem to have wider distribution among turtles, than previously thought.


Subject(s)
Animal Shells , Osteogenesis , Phylogeny , Turtles , Animals , Turtles/anatomy & histology , Turtles/embryology , Animal Shells/anatomy & histology , Animal Shells/growth & development , Animal Shells/embryology , Osteogenesis/physiology , Biological Evolution , Neural Crest/embryology , Mesoderm/embryology
2.
Dev Biol ; 515: 7-17, 2024 Nov.
Article in English | MEDLINE | ID: mdl-38942110

ABSTRACT

In most mollusks (conchiferans), the early tissue responsible for shell development, namely, the shell field, shows a common process of invagination during morphogenesis. Moreover, lines of evidence indicated that shell field invagination is not an independent event, but an integrated output reflecting the overall state of shell field morphogenesis. Nevertheless, the underlying mechanisms of this conserved process remain largely unknown. We previously found that actomyosin networks (regularly organized filamentous actin (F-actin) and myosin) may play essential roles in this process by revealing the evident aggregation of F-actin in the invaginated region and demonstrating that nonmuscle myosin II (NM II) is required for invagination in the gastropod Lottia peitaihoensis (= Lottia goshimai). Here, we investigated the roles of the Rho family of small GTPases (RhoA, Rac1, and Cdc42) to explore the upstream regulators of actomyosin networks. Functional assays using small molecule inhibitors suggested that Cdc42 modulates key events of shell field morphogenesis, including invagination and cell rearrangements, while the roles of RhoA and Rac1 may be nonspecific or negligible. Further investigations revealed that the Cdc42 protein was concentrated on the apical side of shell field cells and colocalized with F-actin aggregation. The aggregation of these two molecules could be prevented by treatment with Cdc42 inhibitors. These findings suggest a possible regulatory cascade of shell field morphogenesis in which Cdc42 recruits F-actin (actomyosin networks) on the apical side of shell field cells, which then generates resultant mechanical forces that mediate correct shell field morphogenesis (cell shape changes, invagination and cell rearrangement). Our results emphasize the roles of the cytoskeleton in early shell development and provide new insights into molluscan shell evolution.


Subject(s)
Actins , Actomyosin , Animal Shells , Gastropoda , Morphogenesis , cdc42 GTP-Binding Protein , Animals , Gastropoda/embryology , Gastropoda/metabolism , Animal Shells/metabolism , Animal Shells/growth & development , Animal Shells/embryology , Actins/metabolism , Actomyosin/metabolism , cdc42 GTP-Binding Protein/metabolism , Myosin Type II/metabolism , rhoA GTP-Binding Protein/metabolism
3.
J Therm Biol ; 100: 103046, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34503793

ABSTRACT

The Mediterranean Triton Charonia seguenzae (Aradas and Benoit, 1870) is an endangered marine gastropod. Re-establishment of C. seguenzae populations in the depleted habitats requires knowledge of its biology and breeding in captivity. Deformities have a huge impact on offspring survival and quality. Temperature has been recorded to affect the development of deformities in marine gastropods. The present study aims to identify the stage of development at which deformities occur, under four temperature regimes (17, 23, 26 and 29 °C). At the stages of trochophore, veliger and free veliger larvae, three capsules that were acclimated at the examined temperatures at the stage of morula were collected, opened and 50 larvae per capsule sampled. Deformities were observed at every examined developmental stage under all tested temperatures. The lower rate of deformities at every stage occurred at 23 °C. The higher tested temperature (29 °C) was lethal and at the lower tested temperature (17 °C) almost every specimen was deformed (96.66%) at eclosion. The effect of acclimation at four developmental stages (morula, trochophore, shell formation and veliger) on the development of deformities at the free veligers of Charonia seguenzae, was studied under three temperature conditions (17, 26 and 29 °C). At eclosion, three capsules were collected, opened and 50 larvae per capsule were sampled. The acclimation at morula and trochophore larva stages led to the higher rates of deformities at eclosion. The size of the free veliger larvae was also affected by temperature with maximum size at eclosion observed at 23 °C. Charonia seguenzae's embryos tolerate elevated temperatures within environmental limits (26 °C) but near future global warming will probably pose a threat to their survival. The free veliger larvae survival at the environmental minimum is related to the time window of the acclimation, since Triton's embryos are more vulnerable to temperature alterations during the early developmental stages.


Subject(s)
Animal Shells/abnormalities , Gastropoda/embryology , Temperature , Thermotolerance , Animal Shells/embryology , Animals , Gastropoda/physiology , Larva/growth & development , Larva/physiology
4.
J Morphol ; 282(4): 543-552, 2021 04.
Article in English | MEDLINE | ID: mdl-33491791

ABSTRACT

Turtles are characterized by their typical carapace, which is primarily composed of corneous beta proteins in the horny part and collagen in the dermal part. The formation of the extracellular matrix in the dermis of the carapace in a hard-shelled and a soft-shelled turtle has been compared. The study examines carapace development, with an emphasis on collagen accumulation, in the soft-shelled turtle Pelodiscus sinensis and hard-shelled turtle Trachemys scripta elegans, using comparative morphological and embryological analyses. The histological results showed that collagen deposition in the turtle carapace increased as the embryos developed. However, significant differences were observed between the two turtle species at the developmental stages examined. The microstructure of the dermis of the carapace of P. sinensis showed light and dark banding of collagen bundles, with a higher overall collagen content, whereas the carapacial matrix of T. scripta was characterized by loosely packed and thinner collagenous fiber bundles with a lower percentage of type I collagen. Overall, the formation and distribution of collagen fibrils at specific developmental stages are different between the soft-and hard-shelled turtles. These results indicate that the pliable epidermis of the soft-shelled turtle is supported by a strong dermis that is regularly distributed with collagen and that it allows improved maneuvering, whereas a strong but inflexible epidermis as observed in case of hard-shelled turtles limits movement.


Subject(s)
Animal Shells/embryology , Animal Shells/metabolism , Collagen/metabolism , Dermis/metabolism , Turtles/embryology , Animal Shells/cytology , Animals , Collagen/genetics , Epidermis , Gene Expression Regulation , Turtles/anatomy & histology
5.
Insect Sci ; 28(4): 901-916, 2021 Aug.
Article in English | MEDLINE | ID: mdl-32536018

ABSTRACT

Chitinase degrades chitin in the old epidermis or peritrophic matrix of insects, which ensures normal development and metamorphosis. In our previous work, we comprehensively studied the function of SfCht7 in Sogatella furcifera. However, the number and function of chitinase genes in S. furcifera remain unknown. Here, we identified 12 full-length chitinase transcripts from S. furcifera, which included nine chitinase (Cht), two imaginal disc growth factor (IDGF), and one endo-ß-N-acetylglucosaminidase (ENGase) genes. Expression analysis results revealed that the expression levels of eight genes (SfCht3, SfCht5, SfCht6-1, SfCht6-2, SfCht7, SfCht8, SfCht10, and SfIDGF2) with similar transcript levels peaked prior to molting of each nymph and were highly expressed in the integument. Based on RNA interference (RNAi), description of the functions of each chitinase gene indicated that the silencing of SfCht5, SfCht10, and SfIDGF2 led to molting defects and lethality. RNAi inhibited the expressions of SfCht5, SfCht7, SfCht10, and SfIDGF2, which led to downregulated expressions of chitin synthase 1 (SfCHS1, SfCHS1a, and SfCHS1b) and four chitin deacetylase genes (SfCDA1, SfCDA2, SfCDA3, and SfCDA4), and caused a change in the expression level of two trehalase genes (TRE1 and TRE2). Furthermore, silencing of SfCht7 induced a significant decrease in the expression levels of three wing development-related genes (SfWG, SfDpp, and SfHh). In conclusion, SfCht5, SfCht7, SfCht10, and SfIDGF2 play vital roles in nymph-adult transition and are involved in the regulation of chitin metabolism, and SfCht7 is also involved in wing development; therefore, these genes are potential targets for control of S. furcifera.


Subject(s)
Chitinases/genetics , Hemiptera , Metamorphosis, Biological/genetics , Acetylglucosaminidase/genetics , Animal Shells/embryology , Animal Shells/growth & development , Animals , Gene Expression Regulation, Developmental , Genes, Insect , Hemiptera/embryology , Hemiptera/genetics , Hemiptera/physiology , Imaginal Discs/embryology , Intercellular Signaling Peptides and Proteins/genetics , Molting/genetics , Nymph/growth & development , Nymph/physiology , Wings, Animal/embryology , Wings, Animal/growth & development
6.
J Exp Zool A Ecol Integr Physiol ; 333(9): 629-636, 2020 11.
Article in English | MEDLINE | ID: mdl-32894008

ABSTRACT

The Ogasawara Islands are an important rookery for the green turtle (Chelonia mydas) in the North Pacific. Green turtles possess temperature-dependent sex determination, and warmer incubation temperatures produce more females than males. Therefore, conservation practices such as nest shading may be required for this population to mitigate the effect of global warming on their sex ratio. To consider the application of such conservation practices in the Ogasawara population, it is fundamental to understand how artificially modified nest environments will affect green turtle hatchling phenotypes that influence their fitness. Here, we investigated the effects of nest shading on green turtle hatchling phenotypes in the Ogasawara population by using a split clutch experiment equally separating the clutch, relocating each half-clutch into an outdoor hatchery area either with or without shading, and observing the subsequent hatchling phenotype. Our results showed that the shading treatment produced hatchlings with a better self-righting response and a larger carapace size. Additionally, the shading treatment mostly reduced the production of hatchlings with a nonmodal scute pattern and produced hatchlings with a smaller unabsorbed yolk sac, which may be associated with their residual yolk mass. These results suggest that conservation practices such as shading could alter not only the sex ratio but also the hatchling phenotype that influences their fitness. Hence, our results suggest that applications of such conservation strategies must be carefully considered.


Subject(s)
Temperature , Turtles/embryology , Animal Shells/embryology , Animals , Conservation of Natural Resources/methods , Female , Japan , Locomotion , Male , Phenotype , Turtles/physiology , Yolk Sac
7.
Sci Rep ; 9(1): 16439, 2019 11 11.
Article in English | MEDLINE | ID: mdl-31712739

ABSTRACT

In vertebrates, the steroidogenesis enzyme 5α-reductase converts testosterone to the more potent androgen 5α-dihydrotestosterone. Homologues of 5α-reductase genes have been identified in molluscs. However, recent findings suggest that vertebrate-type steroid androgens are not utilised in molluscan reproductive development. Genomic searches have revealed that molluscs do not possess many of the steroidogenic enzymes required to make testosterone, nor a nuclear androgen receptor. Consequently, the role of 5α-reductase in molluscs presents a mystery. Here, developmental exposures of Biomphalaria glabrata to selective pharmaceutical 5α-reductase inhibitors elicited a strong, highly reproducible phenotypic response characterised by the development of elongated "banana-shaped" shell morphology. In comparison to untreated snails, the shells are open-coiled and the whorls are unattached. Dutasteride (5α-reductase inhibitor) is approximately 10-times more potent at provoking the banana-shaped shell phenotype than finasteride, paralleling the pharmaceuticals' efficacy in humans. Other enzyme inhibitors with different modes of action were tested to investigate the specificity of the phenotype. However, only the pharmaceutical 5α-reductase inhibitors provoked the response. Dutasteride elicited the same phenotype in a second gastropod, Physella acuta. In the absence of evidence for de novo androgen steroidogenesis in molluscs, these findings suggest that novel substrates for 5α-reductase exist in gastropods, lending support to the contention that molluscan endocrinology differs from the well-characterised vertebrate endocrine system.


Subject(s)
5-alpha Reductase Inhibitors/pharmacology , Animal Shells/anatomy & histology , Cholestenone 5 alpha-Reductase/metabolism , Embryonic Development/drug effects , Gastropoda/anatomy & histology , Gastropoda/drug effects , Animal Shells/embryology , Animals , Fresh Water , Gastropoda/embryology , Gastropoda/enzymology , Humans
8.
J R Soc Interface ; 16(158): 20190175, 2019 09 27.
Article in English | MEDLINE | ID: mdl-31480923

ABSTRACT

The cuttlefish shell is an internal structure with a composition and general organization unique among molluscs. Its formation and the structure-function relation are explored during Sepia officinalis development, using computerized axial tomography scanning (CAT-scan) three-dimensional analyses coupled to physical measurements and modelling. In addition to the evolution of the overall form, modifications of the internal structure were identified from the last third embryonic stages to adult. Most of these changes can be correlated to life cycle stages and environmental constraints. Protected by the capsule during embryonic life, the first internal chambers are sustained by isolated pillars formed from the dorsal to the ventral septum. After hatching, the formation of pillars appears to be a progressive process from isolated points to interconnected pillars forming a wall-delineated labyrinthine structure. We analysed the interpillar space, the connectivity and the tortuosity of the labyrinth. The labyrinthine pillar network is complete just prior to the wintering migration, probably to sustain the need to adapt to high pressure and to allow buoyancy regulation. At that time, the connectivity in the pillar network is compensated by an increase in tortuosity, most probably to reduce liquid diffusion in the shell. Altogether these results suggest adjustment of internal calcified structure development to both external forces and physiological needs.


Subject(s)
Animal Shells/embryology , Embryo, Nonmammalian/embryology , Sepia/embryology , Animal Shells/diagnostic imaging , Animals , Embryo, Nonmammalian/diagnostic imaging , Tomography, X-Ray Computed
9.
Evol Dev ; 21(6): 297-310, 2019 11.
Article in English | MEDLINE | ID: mdl-31441599

ABSTRACT

A key trend in the 210-million-year-old history of modern turtles was the evolution of shell kinesis, that is, shell movement during neck and limb retraction. Kinesis is hypothesized to enhance predator defense in small terrestrial and semiaquatic turtles and has evolved multiple times since the early Cretaceous. This complex phenotype is nonfunctional and far from fully differentiated following embryogenesis. Instead, kinesis develops slowly in juveniles, providing a unique opportunity to illustrate the postembryonic origins of an adaptive trait. To this end, we examined ventral shell (plastral) kinesis in emydine box turtles and found that hatchling plastron shape differs from that of akinetic-shelled relatives, particularly where the hinge that enables kinesis differentiates. We also demonstrated shape changes relative to plastron size in juveniles, coinciding with a shift in the carapace-plastron structural connection, rearrangement of ectodermal plates, and bone repatterning. Furthermore, because the shell grows larger relative to the head, complete concealment of the head and extremities is only achieved after relative shell proportions increase. Structural alterations that facilitate the box turtle's transformation are probably prepatterned in embryos but require function-induced changes to differentiate in juveniles. This mode of delayed trait differentiation is essential to phenotypic diversification in turtles and perhaps other tetrapods.


Subject(s)
Animal Shells/embryology , Embryonic Development , Turtles/embryology , Animals
10.
J Anat ; 235(4): 836-846, 2019 10.
Article in English | MEDLINE | ID: mdl-31198986

ABSTRACT

Turtle horny shell has a scute pattern, which is conservative through evolution and across species. The discovery of epidermal placodes as the scute primordia and their strict topographical association to the somites of the turtle embryo suggested a new interpretation of the developmental mechanism of the scute pattern. Here, we tested the hypothesis that horny scutes develop from a mosaic of placodes corresponding exactly to the paths of myoseptae, with vertebral and pleural scutes developing staggered in adjacent segments, and marginal scutes developing in every segment. This scheme predicts little variation in marginals and suggests intercalary supernumerary scutes as potential variations for the vertebral and pleural rows. We examined spatial and numerical variations of the horny shell in 655 newly hatched olive ridley sea turtle, Lepidochelys olivacea, which is known to have a highly variable horny shell. In total, 120 patterns of carapacial scutes and 10 patterns of scutes on plastron, differing in the number and position of scutes were found. The number of vertebral scutes varied from 4 to 10. Variations with five, six and seven vertebrals occurred with the greatest and nearly equally frequency (31.5% on average). Pleural scutes were from 5 to 10 at one or both sides, and the typical symmetric pattern for sea turtles with five pairs of pleurals was only seen in ca. 12% of specimens. In contrast, the majority of the specimens (92.7%) had just 13 pairs of marginals, showing a stable normal pattern. Similarly, on plastron the horny scutes were conservative, too; about 85% of specimens standardly had six pairs of plastral scutes and all specimens had four pairs of inframarginals. Despite a high level of variation of vertebral and pleural scutes in olive ridley turtle, all patterns fall into the theoretical spectrum of possible variants predicted by the segment-dependent model of development of the turtle horny shell. Therefore, the results of our analysis support the existence of direct morphogenetic correlation between the number and distribution of normal and supernumerary scutes and metamere organization of the turtle embryo.


Subject(s)
Animal Shells/embryology , Turtles/embryology , Animals
11.
Biol Rev Camb Philos Soc ; 93(1): 270-283, 2018 02.
Article in English | MEDLINE | ID: mdl-28560755

ABSTRACT

An exhaustive study of existing data on the relationship between egg size and maximum size of embryonic shells in 42 species of extant cephalopods demonstrated that these values are approximately equal regardless of taxonomy and shell morphology. Egg size is also approximately equal to mantle length of hatchlings in 45 cephalopod species with rudimentary shells. Paired data on the size of the initial chamber versus embryonic shell in 235 species of Ammonoidea, 46 Bactritida, 13 Nautilida, 22 Orthocerida, 8 Tarphycerida, 4 Oncocerida, 1 Belemnoidea, 4 Sepiida and 1 Spirulida demonstrated that, although there is a positive relationship between these parameters in some taxa, initial chamber size cannot be used to predict egg size in extinct cephalopods; the size of the embryonic shell may be more appropriate for this task. The evolution of reproductive strategies in cephalopods in the geological past was marked by an increasing significance of small-egged taxa, as is also seen in simultaneously evolving fish taxa.


Subject(s)
Animal Shells/embryology , Biological Evolution , Cephalopoda/embryology , Animals , Fossils , Reproduction
12.
Integr Comp Biol ; 57(6): 1303-1311, 2017 12 01.
Article in English | MEDLINE | ID: mdl-28992039

ABSTRACT

The turtle shell is often described as an evolutionary novelty that facilitated the radiation of the clade Testudines. The scutes, or keratinous plates, of the turtle shell are hypothesized to be patterned by reaction-diffusion dynamics, and this property of their development provides explanatory power to mechanisms of anomalous variation. A mathematical model of scute development predicts that anomalous variation in the phylogenetically stable pattern of scutes is achieved by environmental influence on the developmental program. We test this prediction with data on patterns of scute variation from natural nests and controlled incubation of sea turtle eggs in Florida and Western Australia. We find that high temperatures are sufficient to produce anomalous patterns in turtle scutes, and that this correlation is even stronger when conditions are dry. Furthermore, we find that the patterns of variation are not random; greater anomalous variation is found in the midline vertebral scutes and during a critical period of turtle development.


Subject(s)
Animal Shells/embryology , Animal Shells/growth & development , Biological Evolution , Turtles/embryology , Turtles/growth & development , Animals , Computer Simulation , Florida , Ovum/growth & development , Temperature , Western Australia
14.
Arthropod Struct Dev ; 46(1): 77-95, 2017 Jan.
Article in English | MEDLINE | ID: mdl-27816526

ABSTRACT

The crustacean cuticle is a chitin-based extracellular matrix, produced in general by epidermal cells and ectodermally derived epithelial cells of the digestive tract. Cuticle morphogenesis is an integrative part of embryonic and postembryonic development and it was studied in several groups of crustaceans, but mainly with a focus on one selected aspect of morphogenesis. Early studies were focused mainly on in vivo or histological observations of embryonic or larval molt cycles and more recently, some ultrastructural studies of the cuticle differentiation during development were performed. The aim of this paper is to review data on exoskeletal and gut cuticle formation during embryonic and postembryonic development in crustaceans, obtained in different developmental stages of different species and to bring together and discuss different aspects of cuticle morphogenesis, namely data on the morphology, ultrastructure, composition, connections to muscles and molt cycles in relation to cuticle differentiation. Based on the comparative evaluation of microscopic analyses of cuticle in crustacean embryonic and postembryonic stages, common principles of cuticle morphogenesis during development are discussed. Additional studies are suggested to further clarify this topic and to connect the new knowledge to related fields.


Subject(s)
Crustacea/embryology , Crustacea/physiology , Insect Proteins/physiology , Molting , Morphogenesis , Animal Shells/embryology , Animal Shells/physiology , Animals , Calcinosis , Chitin/chemistry , Developmental Biology , Embryonic Development , Epithelial Cells , Intestines/embryology , Intestines/physiology , Larva/physiology , Microscopy, Electron, Transmission
15.
Environ Toxicol Chem ; 35(9): 2339-48, 2016 09.
Article in English | MEDLINE | ID: mdl-26887568

ABSTRACT

The aim of the present study was to investigate the lethal and sublethal effects of prednisolone exposure on the embryonic and posthatching stage of the freshwater snail, Physa acuta. The egg masses were exposed for 14 d to prednisolone concentrations ranging from 15.6 µg/L to 1000 µg/L. Treatment with prednisolone at 125 µg/L to 1000 µg/L resulted in significant decline in growth, survival, and heart rate, as well as notable abnormalities in embryonic development. Premature embryonic hatching was observed at lower concentrations of 31.25 µg/L and 62.5 µg/L, whereas delayed hatching was seen at concentrations from 125 µg/L to 1000 µg/L. To assess impacts of prednisolone exposure on the hatched juveniles, the drug exposure was extended for another 28 d. Impairment of shell development was noted in juveniles exposed to concentrations from 62.5 µg/L to 1000 µg/L at the end of 42 d, which resulted in thin and fragile shells. The thickness of shells in snails exposed to 1000 µg/L was significantly lower in comparison to those in the 15.6-µg/L and control treatments. In addition, lower calcium concentration in shells of the exposed juvenile snails at treatments of 62.5 µg/L to 1000 µg/L consequently reduced their growth. The present study confirms that continuous exposure to prednisolone can result in deleterious effects on calcium deposition, resulting in shell thinning in the freshwater snail P. acuta. Environ Toxicol Chem 2016;35:2339-2348. © 2016 SETAC.


Subject(s)
Animal Shells/drug effects , Embryo, Nonmammalian/drug effects , Prednisolone/toxicity , Snails/drug effects , Water Pollutants, Chemical/toxicity , Animal Shells/embryology , Animals , Dose-Response Relationship, Drug , Embryo, Nonmammalian/embryology , Fresh Water/chemistry , Snails/growth & development
16.
Biol Lett ; 11(4): 20150022, 2015 Apr.
Article in English | MEDLINE | ID: mdl-25878046

ABSTRACT

Recent efforts to decipher the enigma of the turtle's shell revealed that distantly related turtle species deploy diverse processes during shell development. Even so, extant species share in common a shoulder blade (scapula) that is encapsulated within the shell. Thus, evolutionary change in the correlated development of the shell and scapula probably underpins the evolution of highly derived shell morphologies. To address this expectation, we conducted one of the most phylogenetically comprehensive surveys of turtle development, focusing on scapula growth and differentiation in embryos, hatchlings and adults of 13 species. We report, to our knowledge, the first description of secondary differentiation owing to skeletal remodelling of the tetrapod scapula in turtles with the most structurally derived shell phenotypes. Remodelling and secondary differentiation late in embryogenesis of box turtles (Emys and Terrapene) yielded a novel skeletal segment (i.e. the suprascapula) of high functional value to their complex shell-closing system. Remarkably, our analyses suggest that, in soft-shelled turtles (Trionychidae) with extremely flattened shells, a similar transformation is linked to truncated scapula growth. Skeletal remodelling, as a form of developmental plasticity, might enable the seemingly constrained turtle body plan to diversify, suggesting the shell is not an evolutionary straitjacket.


Subject(s)
Animal Shells/embryology , Animal Shells/growth & development , Bone Development , Turtles/embryology , Turtles/growth & development , Animals , Embryo, Nonmammalian , Embryonic Development , Phylogeny , Scapula/embryology , Scapula/growth & development
17.
J Exp Zool B Mol Dev Evol ; 324(3): 221-9, 2015 May.
Article in English | MEDLINE | ID: mdl-25877335

ABSTRACT

The turtle shell is composed of dorsal armor (carapace) and ventral armor (plastron) covered by a keratinized epithelium. There are two epithelial appendages of the turtle shell: scutes (large epidermal shields separated by furrows and forming a unique mosaic) and tubercles (numerous small epidermal bumps located on the carapaces of some species). In our perspective, we take a synthetic, comparative approach to consider the homology and evolution of these integumental appendages. Scutes have been more intensively studied, as they are autapomorphic for turtles and can be diagnostic taxonomically. Their pattern of tessellation is stable phylogenetically, but labile in the individual. We discuss the history of developmental investigations of these structures and hypotheses of evolutionary and anomalous variation. In our estimation, the scutes of the turtle shell are an evolutionary novelty, whereas the tubercles found on the shells of some turtles are homologous to reptilian scales.


Subject(s)
Animal Shells/anatomy & histology , Biological Evolution , Turtles/anatomy & histology , Animal Shells/embryology , Animals , Epidermis/anatomy & histology , Epidermis/embryology , Paleontology , Turtles/embryology
18.
J Exp Zool B Mol Dev Evol ; 324(3): 208-20, 2015 May.
Article in English | MEDLINE | ID: mdl-25675951

ABSTRACT

Two of the major controversies in the present study of turtle shell development involve the mechanism by which the carapacial ridge initiates shell formation and the mechanism by which each rib forms the costal bones adjacent to it. This paper claims that both sides of each debate might be correct-but within the species examined. Mechanism is more properly "mechanisms," and there is more than one single way to initiate carapace formation and to form the costal bones. In the initiation of the shell, the rib precursors may be kept dorsal by either "axial displacement" (in the hard-shell turtles) or "axial arrest" (in the soft-shell turtle Pelodiscus), or by a combination of these. The former process would deflect the rib into the dorsal dermis and allow it to continue its growth there, while the latter process would truncate rib growth. In both instances, though, the result is to keep the ribs from extending into the ventral body wall. Our recent work has shown that the properties of the carapacial ridge, a key evolutionary innovation of turtles, differ greatly between these two groups. Similarly, the mechanism of costal bone formation may differ between soft-shell and hard-shell turtles, in that the hard-shell species may have both periosteal flattening as well as dermal bone induction, while the soft-shelled turtles may have only the first of these processes.


Subject(s)
Animal Shells/embryology , Ribs/embryology , Turtles/embryology , Animal Shells/anatomy & histology , Animals , Biological Evolution , Phylogeny , Ribs/anatomy & histology , Turtles/anatomy & histology
19.
J Exp Zool B Mol Dev Evol ; 324(3): 244-54, 2015 May.
Article in English | MEDLINE | ID: mdl-25052382

ABSTRACT

The shoulder girdle in turtles is encapsulated in the shell and has a triradiate morphology. Due to its unique configuration among amniotes, many theories have been proposed about the skeletal identities of the projections for the past two centuries. Although the dorsal ramus represents the scapular blade, the ventral two rami remain uncertain. In particular, the ventrorostral process has been compared to a clavicle, an acromion, and a procoracoid based on its morphology, its connectivity to the rest of the skeleton and to muscles, as well as with its ossification center, cell lineage, and gene expression. In making these comparisons, the shoulder girdle skeleton of anurans has often been used as a reference. This review traces the history of the debate on the homology of the shoulder girdle in turtles. And based on the integrative aspects of developmental biology, comparative morphology, and paleontology, we suggest acromion and procoracoid identities for the two ventral processes.


Subject(s)
Shoulder/anatomy & histology , Turtles/anatomy & histology , Anatomy, Comparative , Animal Shells/anatomy & histology , Animal Shells/embryology , Animals , Anura/anatomy & histology , Biological Evolution , Scapula/anatomy & histology , Scapula/embryology , Shoulder/embryology , Shoulder Joint/anatomy & histology , Shoulder Joint/embryology , Turtles/embryology
20.
J Exp Zool B Mol Dev Evol ; 324(3): 169-80, 2015 May.
Article in English | MEDLINE | ID: mdl-25074288

ABSTRACT

Many evo-devo studies of the turtle's shell draw hypotheses and support from historical sources. The groundbreaking works of Cuvier, Geoffroy St. Hilaire, Carus, Rathke, Owen, and others are being revived in modern research, and their centuries-old understanding of the turtle's shell reconsidered. In the works of these eminent biologists of the 19th century, comparative anatomy and embryology of turtle morphology set the stage for future studies in developmental biology, histology, and paleontology. Given the impact that these works still make on modern research, it is important to develop a thorough appreciation of previous authors, regarding how they arrived at their conclusions (i.e., what counted as evidence?), whether there was debate amongst these authors about shell development (i.e., what counted as an adequate explanation?), and even why these men, some of the most powerful and influential thinkers and anatomists of their day, were concerned with turtles. By tracing and exposing the context and content of turtle shell studies in history, our aim is to inform modern debates about the evolution and development of the turtle's shell.


Subject(s)
Anatomy, Comparative/history , Developmental Biology/history , Turtles/anatomy & histology , Turtles/embryology , Animal Shells/anatomy & histology , Animal Shells/embryology , Animals , Biological Evolution , History, 19th Century
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