Structure of the shell and tertiary membranes of eggs of softshell turtles (Trionyx spiniferus)

Eggs of the turtle Trionyx spiniferus are rigid, calcareous spheres averaging 2.5 cm in diameter. The eggshell is morphologically very similar to avian eggshells. The outer crystalline layer is composed of roughly columnar aggregates, or shell units, of calcium carbonate in the aragonite form. Each shell unit tapers to a somewhat conical tip at its base. Interior to the crystalline layer are two tertiary egg membranes: the outer shell membrane and the inner shell membrane. The outer shell membrane is firmly attached to the inner surface of the shell, and the two membranes are in contact except at the air cell, where the inner shell membrane separates from the outer shell membrane. Both membranes are multi-layered, with the inner shell membrane exhibiting a more fibrous structure than the outer shell membrane. Numerous pores are found in the eggshell, and these generally occur at the intersection of four or more shell units.     

Ultrastructural morphology of the shell and shell membrane of eggs of common snapping turtles (Chelydra serpentina)

Common snapping turtles (Chelydra serpentina) lay nearly spherical, flexible-shelled eggs having an outer mineral layer composed of calcium carbonate in the aragonite form. The mineral layer is arranged into loosely organized groups of nodular shell units, with numerous spaces (or pores) between adjacent shell units. Shell units are structurally complex, consisting of an inner tip that is morphologically distinct from the main body of the shell unit. Contained within an intact shell unit at the interface of the tip and the main part of the shell unit is the central plaque, an apparent modification of the shell membrane that may serve to nucleate calcification of shell units during shell formation. The tips of shell units are firmly attached to a single, multilayered shell membrane throughout much of incubation. The calcareous layer begins to detach from the shell membrane about half-way through incubation, and changes in shell morphology attending this detachment indicate that snapping turtles may use the shell as a source of calcium during embryogenesis. The arrangement of the mineral layer into groups of shell units, the large number of spaces between shell units, and little or no interlocking of crystallites of adjacent shell units apparently are factors contributing to the ability of these eggs to swell as they absorb water.     

Ontogeny of the Molluscan Shell Field: a Review

In the gastropod, scaphopod, lamellibranch, and cephalopod gastrulae a thickened portion of the posttrochal region is referred to as the embryonic shell field. It invaginates and gives rise to the shell gland. In species with an at least temporarily external shell, the shell gland evaginates and again forms a shell field. In lamellibranchs, the shell field grows into two halves connected by the ligament-secreting isthmus. In polyplacophorans plate fields are produced without invagination. Slugs and endocochleate cephalopods overgrow the embryonic shell field to form an internal shell sac. The calcified part of the shell is secreted by the flattened central region. The periostracum has its origin in the permanently thickened peripheral region of the shell field. In many forms, this region is depressed in a periostracal groove. If the shell is external, the central region of flattened cells, the mantle roof, along with the two or three marginal folds of the free mantle edge and, in species with internal shell, the shell sac are parts of the mantle. The shell field descends from the first somatoblasts. Either of 2 d or 2 c alone is able to form the shell field. There are arguments that the formation of the embryonic shell field is not autonomic, but induced by the entoderm during a period of contact. The shell gland and the shell field grow by mitotic cell divisions. Cells secreting organic material are highly prismatic, have a well developed ergastoplasm and large dictyosornes, and contain much peroxidase. The secretion of calcium manifests itself in very flat cells, rich in alkaline phosphatase and glycogen. The shell gland and the rosette of ectocochleate conchifera together are homologous to the proximal part of the shell sac in slugs and endocochleate cephalopods.     

Optimal growth pattern of defensive organs: the diversity of shell growth among mollusks

Mollusks show a diversity of shell growth patterns. We develop a model for the dynamic resource allocation to defense organs and analyze it with the Pontryagin maximum principle. A typical optimal growth schedule is composed of the initial phase of soft-body growth without shell followed by a simultaneous growth of shell and soft body and finally the reproductive phase without growth (simultaneous shell growth). If the defensible predation risk is low or if the cost of defense is high, the optimal strategy is to have no shell (shell-less growth). If defensible predation pressure or general mortality differs before and after maturation, an additional three strategies, characteristic of the exclusive growth of shell or soft body, can be optimal (sequential shell growth, additional body-expansion growth, and additional callus-building growth). These optimal strategies are in accord with the patterns observed for mollusks. In particular, the growth strategies with exclusive growth phase of external shells are preferred when durophagous predation pressure after maturation is higher than that before maturation. This result explains the observation that many tropical gastropods with thickened shell lips spend their vulnerable juvenile phase in sheltered habitats.     

Analysis of repeated signals during shell fights in the hermit crab Pagurus bernhardus

Shell exchanges between hermit crabs may occur after a period of shell rapping, when the initiating or attacking crab brings its shell rapidly and repeatedly into contact with the shell of the non-initiator or defender, in a series of bouts. There are two opposing models of hermit crab shell exchange and the function of shell rapping. The negotiation model views shell exchange as a mutualistic activity, in which the initiator supplies information about the quality of its shell via the fundamental frequency of the rapping sound. The aggression model views shell rapping as either detrimental to the defending crab, or as providing it with information about the initiator''s ability or motivation to continue, or both. The negotiation model makes no predictions about the temporal pattern of rapping, but under the aggression model it would be expected that crabs that rapped more vigorously would be more likely to effect an exchange. Repeating the signal could be expected under either model. Crabs that achieve an exchange rap more vigorously, rapping is more persistent when a clear gain in shell quality may be achieved, and the vigour is greater when the relative resource-holding potential (or ''fighting ability'') is high. These findings support the aggression model rather than the negotiation model. Contrary to the predictions of game theory, crabs that do not effect an exchange appear to signal that they are about to give up. The data suggest that rapping is performed repeatedly because the accumulation of all of the performances acts as a signal of stamina.     

Aspects of shell formation in eggs of the tuatara,Sphenodon punctatus

The flexible shell from eggs of the tuatara (Sphenodon punctatus) is comprised of both calcareous and fibrous components. The calcareous material is organized into columns that extend deep into the fibrous shell membrane. Many of the fibers of the membrane are enclosed within the crystalline matrix of the columns. Columns widen and flatten slightly at the outer surface of the eggshell to form cap-like structures composed of a compact crystalline matrix containing no fibers. The outer surface of eggs laid prior to completion of shell formation consists of a series of nodes obscured by a densely fibrous matrix. Similar nodes also are found at the inner surface of partially shelled eggs. The nodes represent the outer and inner aspects of columns that had not completed formation prior to oviposition. Our interpretation is that a layer (or layers) of the shell membrane forms first, with nucleation of columns occurring shortly thereafter. Columns grow into the membrane a short distance and enclose fibers of the membrane, but the primary direction of column growth is toward what will become the outer aspect of the shell. Calcareous columns and the shell membrane form more or less in concert until crystal growth outstrips that of the membrane and a cap-like apex of compact crystalline material is formed. The end result is an eggshell in which the shell membrane and calcareous material form a single unit for much of the thickness of the shell.     

Resource assessment in hermit crabs: the worth of their own shell

Animals gather information about the quality of a resource throughits assessment and behave accordingly as a result of adaptivemotivational changes. In the hermit crab Pagurus longicarpus,we investigated whether an individual was affected in its motivationto acquire a new shell by the quality of the domicile shell(own resource value [ORV]), of the offered shell (external resourcevalue [ERV]), or of both and asked whether its motivation wasaltered by the information gathered during shell investigation.We analyzed the behavior of hermit crabs inhabiting shells ofdiffering qualities and compared their willingness to acquirean offered shell—optimal, smaller than optimal, or largerthan optimal—by measuring the latency to approach it,the number of shell investigation, and its total duration. Crabsin smaller shells (SSs) approached more quick and often theoffered shell, whereas crabs in larger shells investigated theoffered shell more thoroughly. The readiness of crabs to approachthe offered shell and the extent of its investigation were independentof the ERV but were exclusively affected by the ORV, whereasthe number and duration of shell investigation did not changewith time as investigation proceeded, except for crabs in SSs.These results suggest that P. longicarpus' motivation to acquirea new shell is exclusively influenced by the value of the shellit inhabits rather than by the quality of the shell it is offeredand that this species does not gather—or does not use—informationabout ERV during investigation.     

A multivariate study of geographic variation in the whelk Dicathais

An analysis has been made of the variation in shell shape and shell characteristics of 889 Australian and New Zealand specimens of the genus Dicathais, using multivariate techniques. Shell measurements taken were: the overall length, length of spire, length of aperture, and width of aperture. Weight of the shell plus the preserved animal was also recorded. The sculpture of the shell, thickness of the lip, and the presence or absence of a reddish or purplish colouration or banding on the inside of the lip, were assessed qualitatively.Principal component analyses of the size measurements for each site showed that the first principal component, which accounted for greater than 95% of the variation at each site, was associated with variation in the ‘size’ of the animal. Canonical analysis of the size measurements showed a cline in shell shape from the animals on the western side of Australia to those on the eastern side of Australia and New Zealand. The resulting canonical variates were associated with variation in the ‘shape’ of the shell. Principal component analyses of the between-group matrix and of the within-group matrix of the size measurements showed that the site means exhibited a similar pattern of dispersion to that of the animals within each site.Canonical analysis of the shell characteristics showed that variation along the first canonical axis was largely produced by shell sculpture, while variation along the second resulted from differences in colouration/banding.The generalized variances of the correlation matrices for the size measurements showed that groups with similar shell shape were associated with the presence of granite substrata and/or mussel beds or, alternatively, with limestone substrata, but canonical correlation analysis of the relationship between the size measurements and shell characteristics showed that no consistent trend was evident over all sites.A subjective examination of the structure of the radula of 84 animals showed that two distinct morphological forms were present, but that they were not correlated either with sex or any of the named shell forms or site groupings.An analysis of the growth curves of 27 animals of the two forms from the eastern and western coasts of Australia, held in the laboratory, was carried out. The eastern coast form showed a loss of sculpturing and a change in shell shape when kept under west coast conditions and on a mussel diet.Water temperature, diet, substratum, and degree of exposure to wave action were all found to show associations with variations in either shell shape or shell characteristics. It is suggested that the selective force of the habitat which produces changes in shell shape and shell characteristics of the animals at any site is a complex of factors, many of which are interrelated. The genetic basis for the development of shell shape and production of the shell characteristics in Dicathais may be similar to that found in Nucella lapillus (L.) in the Northern Hemisphere.These data suggest that the Dicathais found at the sites studied in this investigation are all part of the same ‘population’, the shell shape and shell characteristics of the adult populations being determined both by selection and phenotypic expressions caused by the selective force of the habitat at each site. It is concluded that the genus consists of a single highly variable species.The value of the application of multivariate analyses to this type of study is shown to lie in the way in which the techniques provide an overall picture of the variation within sites and of the variation between sites.     

The power of shell rapping influences rates of eviction in hermit crabs

Hermit crabs fight for ownership of shells, and shell exchangemay occur after a period of shell rapping, involving the initiatingor attacking crab bringing its shell rapidly and repeatedlyinto contact with the shell of the noninitiator or defender,in a series of bouts. The temporal pattern of rapping containsinformation about the motivation and/or relative resource holdingpotential (RHP) of the initiator and acts as a repeated signalof stamina. Here we investigated the role of the force withwhich the rapping is performed and how this is related to thetemporal pattern of rapping by rubberizing the external surfaceof shells. Initiators that are prevented from rapping withtheir usual level of force persist with the activity for longer over the whole encounter but use fewer raps per bout and areless likely to effect an exchange than those supplied withcontrol shells. The fact that the force of rapping affectsthe likelihood of a crab being victorious suggests that eitherthe force of rapping contains information about motivation orRHP or that force directly affects noninitiators, reducingtheir ability to maintain an adequate grip on their shells.The data suggest that shell rapping is an agonistic signalrather than one that provides information useful to the noninitiator,as has been suggested by the negotiation model of shell exchange.     

Arch and beam: deployment of microstructural fabrics in relation to loads exerted on the shells of bivalved molluscs in different functional regimes

Two apparently contradictory models have been proposed, relating the disposition of microstructural fabrics of the bivalve shell to stresses they experience. These models are here shown to apply to the function of the shell in different circumstances. In its day-to-day operation, the shell acts as a pair of beams, loaded under opposing stresses exerted by the adductor muscles and the ligament. The resulting strain is built into the shell as new layers are added to its growing interior surface (Wainwright 1969). The distribution of stresses induced by attempts to crush the shell, or by violent adduction intended to prevent it from being opened, is different. Here, the shell acts as a dome, a ‘shell’ in the architect's sense. Compressional stress develops in the outer layer and tension in the inner layer. The distribution of shell microstructures in many bivalves is biomechanically consistent with the need to resist these latter stresses. The shell is prestressed in the right direction to resist this deformation. However, the built-in strain is an exaptation in relation to this function. Any added resistance to crushing it provides is fortuitously advantageous, since it becomes prestressed as an unavoidable consequence of shell growth and articulation.     

淡水贝类贝壳多层构造形成研究

对几种淡水贝（包括蚌、螺）进行形态及组织学观察，并通过实验方法重现贝壳三种物质，即：角质、棱柱质、珍珠质的生成过程，结果表明：外套膜外表皮细胞是由相同类型细胞组成，这些相同细胞在不同的作用条件下形成贝壳多层构造。     

A mathematical consideration for the optimal shell change of hermit crab

Shell of the adult hermit crab has some important roles for its fitness. In the same time, the shell size often limits the body growth of its owner. To grow the body size larger, the individual must change the shell to another larger shell. If the individual cannot get another larger one, the individual has to suppress the body size growth as the occupied shell size allows. Growth suppression would result in the lower fitness. With a simple mathematical model, we consider the criterion about whether the individual should try to change the shell or not in order to get the higher fitness. We show that the optimality of a shell change behavior has a relation with the body size and the season length for the shell change. They also affect the optimal timing for the shell change. It is implied that the probability of the success in a shell change and the cost for the shell change behavior do not affect the optimal timing for the shell change at all but significantly do the optimality of the behavioral choice.     

The MS2 coat protein shell is likely assembled under tension: a novel role for the MS2 bacteriophage A protein as revealed by small-angle neutron scattering

Recombinant forms of the bacteriophage MS2 and its RNA-free (empty) MS2 capsid were analyzed in solution to determine if RNA content and/or the A (or maturation) protein play a role in the global arrangement of the virus protein shell. Analysis of the (coat) protein shell of recombinant versions of MS2 that lack the A protein revealed dramatic differences compared to wild-type MS2 in solution. Specifically, A protein-deficient virus particles form a protein shell of between 31(+/-1) A and 37(+/-1) A. This is considerably thicker than the protein shell formed by either the wild-type MS2 or the RNA-free MS2 capsid, whose protein shells have a thickness of 21(+/-1) A and 25(+/-1) A, respectively. Since the A protein is known to separate from the intact MS2 protein shell after infection, the thin shell form of MS2 represents the pre-infection state, while the post-infection state is thick. Interestingly, these A protein-dependent differences in the virus protein shell are not seen using crystallography, as the crystallization process seems to artificially compact the wild-type MS2 virion. Furthermore, when the A protein is absent from the virus shell (post-infection), the process of crystallization exerts sufficient force to convert the protein shell from the post-infection (thick) state to the pre-infection (thin) conformation. In summary, the data are consistent with the idea that RNA content or amount does not affect the structure of the MS2 virus shell. Rather, the A protein influences the global arrangement of the virus coat dramatically, possibly by mediating the storage of energy or tension within the protein shell during virus assembly. This tension may later be used to eject the MS2 genomic RNA and A protein fragments into the host during infection.     

CAUSE OF BIMODAL DISTRIBUTION IN THE SHAPE OF A TERRESTRIAL GASTROPOD

The distribution of a phenotypic state is often discontinuous and dispersed. An example of such a distribution can be found in the shell shapes of terrestrial gastropods, which exhibit a bimodal distribution whereby species possess either a tall shell or a flat shell. Here we propose a simple model to test the hypothesis that the bimodal distribution relates to the optimum shape for shell balance on the substrates. This model calculates the theoretical shell balance by moment and obtains empirical distribution of shell shape by compiling published data and performing a new analysis. The solution of the model supports one part of the hypothesis, showing that a low-spired shell is the best balanced and is better suited for locomotion on horizontal surface. Additionally, the model shows that both high- and low-spired shells are well balanced and suited on vertical surfaces. The shell with a spire index (shell height divided by diameter) of 1.4 is the least well balanced as a whole. Thus, spire index is expected to show a bimodal distribution with a valley at 1.4. This expectation was supported by empirical distribution of a spire index, suggesting that the bimodality of shell shape in terrestrial gastropods is related to shell balance.     

Shell morphometry in barnacles: quantification of shape and shape change in Balanus

Geometric design in the barnacle genus Balanus has been studied in relation to variation in adult shell form, that includes differences among species, and size-related changes in shape. The genus comprises 40 Recent species, and as a group these display a more or less constant morphology over an extraordinary size range (10 to 200 mm in basal length).
Linear and volumetric measurements were collected from 232 adult individuals of 14 species representing the variation in size, shell form and shell design thought to occur in the genus. Specimens were chosen to represent the size ranges of the species. Only isolated individuals growing on planar surfaces were used; shells were complete, undamaged and undistorted.
Shell form differs among taxa, and no two species scale alike; intraspecific variation for five ratio variables shows strong allometry over the adult size range of each species. As size increases, there is a trend for the basis and orifice to maintain their shapes or to become slightly more elliptical, and for shells to become more conical and proportionately taller.
Throughout their size ranges, species can be described by these geometries: paraboloid (6 species), frustum of an ellipsoidal cone (5 species), frustum of a cone (2 species) and a cone (1 species). Shell geometry is not a function of species size, but there does appear to be a correlation between shell geometry and shell volume. Species with relatively small shell volumes are described by a frustum of an ellipsoidal cone, or by a cone, while those with a relatively large shell volume are described by a paraboloid, or by the frustum of a cone.     

How does life adapt to a gravitational environment? The outline of the terrestrial gastropod shell

How do several characteristics adapt to gravity while mutually influencing each other? Our study addresses this issue by focusing on the terrestrial gastropod shell. The geometric relationship between the spire index (shell height/diameter) and outline (cylindricality) is theoretically estimated. When the shell grows isometrically, a high-spired shell becomes conical in shape and a low-spired shell becomes cylindrical in shape. A physical model shows that the lowest- and highest-spired shells are the most balanced. In addition, a cone shape is the most balanced for a low-spired shell, and a column shape is the most balanced for a high-spired shell. Spire index and cylindricality measured for freshwater gastropods follow the relationship estimated by the model, whereas those for terrestrial gastropods deviate from this relationship. This translates to a high shell being more cylindrical than a flat shell, except in the case of extremely high or low shells. This suggests that the shape of the most balanced shells (lowest and highest shell heights) is constrained by coiling geometry but that relatively unbalanced shells (intermediate shell heights) do not follow a coiling geometry, as a result of adaptation to enable the snail to carry its shell more effectively.     

Genetic analysis of the protein shell of the microcompartments involved in coenzyme B12-dependent 1,2-propanediol degradation by Salmonella

Hundreds of bacterial species use microcompartments (MCPs) to optimize metabolic pathways that have toxic or volatile intermediates. MCPs consist of a protein shell encapsulating specific metabolic enzymes. In Salmonella, an MCP is used for 1,2-propanediol utilization (Pdu MCP). The shell of this MCP is composed of eight different types of polypeptides, but their specific functions are uncertain. Here, we individually deleted the eight genes encoding the shell proteins of the Pdu MCP. The effects of each mutation on 1,2-PD degradation and MCP structure were determined by electron microscopy and growth studies. Deletion of the pduBB', pduJ, or pduN gene severely impaired MCP formation, and the observed defects were consistent with roles as facet, edge, or vertex protein, respectively. Metabolite measurements showed that pduA, pduBB', pduJ, or pduN deletion mutants accumulated propionaldehyde to toxic levels during 1,2-PD catabolism, indicating that the integrity of the shell was disrupted. Deletion of the pduK, pduT, or pduU gene did not substantially affect MCP structure or propionaldehyde accumulation, suggesting they are nonessential to MCP formation. However, the pduU or pduT deletion mutants grew more slowly than the wild type on 1,2-PD at saturating B(12), indicating that they are needed for maximal activity of the 1,2-PD degradative enzymes encased within the MCP shell. Considering recent crystallography studies, this suggests that PduT and PduU may mediate the transport of enzyme substrates/cofactors across the MCP shell. Interestingly, a pduK deletion caused MCP aggregation, suggesting a role in the spatial organization of MCP within the cytoplasm or perhaps in segregation at cell division.     

Description of the early ontogenic part of the Tentaculitids, with implications for classification

Ontogenic development and classification of tentaculitids at high systematic levels are reevaluated in the light of new findings on shell structure and morphology of larval parts, and these features are here regarded as being of primary importance for taxonomy. Class Tentaculita Bouček, 1964 is subdivided into two subclasses, of which subclass Chionioconarida Farsan, 1994 is distinguished by a tubular larval process closed at the apex and covered with microrings. The process is differentiated into a prolarval, metalarval and epilarval part, of which the latter coincides with metamorphosis. Morphology of the larval parts suggests that metamorphosis proceeds in two different manners, giving rise to superorders within this subclass. Within superorder Trompetoconarida Farsan, 1994 a bilaterally symmetrical larval cone develops with an aperture oblique to the long axis of the conch; following metamorphosis the conch becomes radially symmetrical and the aperture perpendicular to the axis; secondary shell, septa and pseudopunctae develop in the adult phase, and the structure of the shell is lamellar. In contrast, within the second superorder, Lirioconarida Farsan, 1994 the epilarval tube develops into a larval bulb with no changes in symmetry and position of the aperture; secondary shell, septa and pseudopuncta are absent. The microstructure of the shell is lamellar in the larval part whereas in postlarval parts it is either sigmoidal or lamellar. The subclass Dacryoconarida Fisher, 1962 possesses a subspherical, tear- or drop-like embryonic chamber which may have a caudal process. The microstructure of the embryonic chamber is variable within this group, being lamellar in some taxa whereas in others, a single layer of shell is present. The postembryonic parts of the lamellar forms possess nacreous or sigmoidal structures.     

根足类原生动物半圆表壳虫壳体生物矿化特征

以有壳阿米巴类原生动物 (肉鞭门 ,叶足纲 )半圆表壳虫 (Arcellahemisphaerica)为研究对象 ,利用光镜和扫描电镜研究了其壳体生物矿化的特征。结果显示 :矿化前期 ,壳体为无色透明且柔软易变形 ;中期 ,为黄色较坚硬 ;后期 ,为褐色坚硬。通过X 射线显微分析术鉴定不同矿化时期壳体的无机元素 ,结果表明 ,与矿化前期相比矿化中期和后期壳体中Si、Mn和Fe的比例增加 ,Cl、K、S和Na的比例减少。由此推测 ,⑴半圆表壳虫矿化过程中壳体坚硬的原因是Si、Mn和Fe的比例增加导致 ,黄色是由微量Mn和Fe引起 ,褐色是高含量Mn与低含量Fe的反映 ;⑵半圆表壳虫壳体矿化以构成壳体的小泡为基本单位进行 ,Si、Mn和Fe矿化体以氧化物形式通过分子间相互作用力 ,与小泡壁上氨基酸或多肽的羟基作用 ,自组装合成。     

Structural Insight into the Mechanisms of Transport across the Salmonella enterica Pdu Microcompartment Shell

Bacterial microcompartments are a functionally diverse group of proteinaceous organelles that confine specific reaction pathways in the cell within a thin protein-based shell. The propanediol utilizing (Pdu) microcompartment contains the reactions for metabolizing 1,2-propanediol in certain enteric bacteria, including Salmonella. The Pdu shell is assembled from a few thousand protein subunits of several different types. Here we report the crystal structures of two key shell proteins, PduA and PduT. The crystal structures offer insights into the mechanisms of Pdu microcompartment assembly and molecular transport across the shell. PduA forms a symmetric homohexamer whose central pore appears tailored for facilitating transport of the 1,2-propanediol substrate. PduT is a novel, tandem domain shell protein that assembles as a pseudohexameric homotrimer. Its structure reveals an unexpected site for binding an [Fe-S] cluster at the center of the PduT pore. The location of a metal redox cofactor in the pore of a shell protein suggests a novel mechanism for either transferring redox equivalents across the shell or for regenerating luminal [Fe-S] clusters.