- Research article
- Open Access
An ancient process in a modern mollusc: early development of the shell in Lymnaea stagnalis
© Hohagen and Jackson; licensee BioMed Central Ltd. 2013
- Received: 4 April 2013
- Accepted: 8 July 2013
- Published: 12 July 2013
The morphological variety displayed by the molluscan shell underlies much of the evolutionary success of this phylum. However, the broad diversity of shell forms, sizes, ornamentations and functions contrasts with a deep conservation of early cell movements associated with the initiation of shell construction. This process begins during early embryogenesis with a thickening of an ectodermal, ‘dorsal’ (opposite the blastopore) population of cells, which then invaginates into the blastocoel to form the shell gland. The shell gland evaginates to form the shell field, which then expands and further differentiates to eventually become the adult shell-secreting organ commonly known as the mantle. Despite the deep conservation of the early shell forming developmental program across molluscan classes, little is known about the fine-scale cellular or molecular processes that underlie molluscan shell development.
Using modern imaging techniques we provide here a description of the morphogenesis of a gastropod shell gland and shell field using the pulmonate gastropod Lymnaea stagnalis as a model. We find supporting evidence for a hypothesis of molluscan shell gland specification proposed over 60 years ago, and present histochemical assays that can be used to identify a variety of larval shell stages and distinct cell populations in whole mounts.
By providing a detailed spatial and temporal map of cell movements and differentiation events during early shell development in L. stagnalis we have established a platform for future work aimed at elucidation of the molecular mechanisms and regulatory networks that underlie the evo-devo of the molluscan shell.
- Alkaline phosphatase
Molluscs constitute one of the most successful, morphologically diverse and ancient phyla of the animal kingdom. They posses an extensive fossil record dating back to the early Cambrian (543+ MYA) and comprise more than 200,000 extant species occupying various marine and terrestrial environments from the deep sea to desert habitats [1, 2]. Much of this evolutionary success can be attributed to the phenotypic plasticity of the external shell which displays an incredible range of mineralogical textures , pigments [4, 5] and ornamentations . This phenotypic diversity is underscored by a diversity in the molecular mechanisms responsible for the construction of the adult shell [7–10].
Despite the morphological and functional-molecular diversity of the adult shell, there is deep conservation of the cellular and morphogenic movements that initiate larval shell secretion (reviewed in ). Importantly, larval shell forming cells are thought to give rise to the fully differentiated adult shell forming organ, the mantle, suggesting that trochophore, veliger and adult gastropod shells do not have independent evolutionary origins as previously suggested . Cell lineage studies in disparate gastropods support a common ontogenetic origin of embryonic, larval and adult gastropod shells; derivatives of the 2d and 2c micromeres in Ilyanassa give rise to the shell gland , and the same lineage of cells in Crepidula fornicata contributes to the mantle of the veliger . Furthermore, veliger mantle cells expressing shell forming genes continue to do so following metamorphosis in the abalone Haliotis asinina[15, 16]. The histochemical properties of larval and adult shell forming organs in L. stagnalis also reveal a similar spatial arrangement of enzymatic activities, suggesting that boundaries of shell forming cell populations established in larval stages are maintained into adult life . Additionally, regulatory genes encoding transcription factors and signalling molecules (such as members of the Hox cluster, engrailed and decapentaplegic) are expressed in embryonic shell forming tissue in disparate molluscan taxa [18–25]. This raises the possibility that extant shelled molluscs may all initiate shell formation using the same developmental program inherited from a distant ancestor, and that it is the downstream shell forming programs operating in the mature mantle which, during evolution, have generated today’s diversity of shelled adult molluscs. If such a scenario were true, this would mean that a common ancestor of the shelled molluscs evolved a developmental program to form a shell which was passed on to all of its future descendants; a 540+ million year old innovation that was of great importance to the future evolutionary success of the phylum.
The pulmonate gastropod Lymnaea stagnalis (Linnaeus, 1758) was once a much used model for understanding both molluscan development in general  and development of the shell in particular . Development of Lymnaea’s shell displays many of the features observed in other gastropod species. Across Molluscan classes, the first morphological sign of shell development is a thickening of the dorsal ectoderm in the post-trochal region of the embryo following gastrulation (see  for a review). Briefly, these dorsal ectodermal cells elongate and are often the only ectodermal cells in contact with the underlying endoderm, specifically cells at the tip of the archenteron (the so called 'small-celled endoderm' due to their lack of large vacuoles present in other endodermal cells [26, 28]). These elongated dorsal ectodermal cells then invaginate to form a ‘shell gland’ [11, 29]. It is during this stage that secretion of the first shell-associated insoluble material takes place. The shell gland subsequently evaginates to form the ‘shell field’, a process during which the contact of ectodermal and endodermal cells is lost, and the first signs of calcification of the previously secreted insoluble material can be observed (e.g. [13, 26, 27, 30]). The initial contact between endoderm and dorsal ectoderm that precedes shell gland invagination has been observed in representatives of the Gastropoda, Bivalvia, Scaphopoda and Cephalopoda (reviewed in ). This contact between dorsal ectoderm and endoderm has lead to the idea that this event is required for the specification of future shell forming cells, and represents a 'true' induction event .
While Raven’s model of shell gland induction  represents the canonical theory of molluscan shell field specification, the molecular mechanisms that initiate and underlie this process remain largely unknown. Molecular analyses that have previously identified transcription factors and signalling molecules in the shell gland and the evaginated and expanding shell field are expressed well after the specification of shell forming cells [19, 21, 24, 31]. We are therefore developing L. stagnalis as a model for molecular investigations into the mechanisms that first specify shell forming cells, and through comparative studies, to enhance our understanding of how the variety of molluscan shells evolved.
Previous cytological studies on the early development of the shell field in L. stagnalis do not include descriptions of the cellular arrangements preceding the first contact between the dorsal ectoderm and the small-celled endoderm at the tip of the archenteron. Here we employ confocal laser scanning microscopy (CLSM) to provide a detailed temporal and spatial description of the morphogenic events associated with development of the larval shell in L. stagnalis. We have also employed histochemical assays based on endogenous peroxidase (PO) and alkaline phosphatase (AP) activity to identify distinct cell populations within the developing shell gland, shell field and other larval structures in whole mounts. These enzymes are known to be active in the shell forming tissues of several molluscan taxa, including L. stagnalis. These assays allow us to trace discrete cell populations in larval shell forming tissues, and may in the future be employed to characterise the effects of experiments aimed at the perturbation of normal shell development. This work represents a platform from which further studies will investigate the molecular processes leading to the specification and differentiation of molluscan shell forming cells.
Cultivation of adult L. stagnalis
Adult specimens of L. stagnalis were collected from the Northeimer Seenplatte near Northeim, Germany (51° 43’ 26.5368’, 9° 57’ 24.75’) and from a pond on the North campus of the University of Göttingen, Germany (51° 33’ 23.727’, 9° 57’ 25.617’). Snails were kept in standard tap water at 25°C, under a 16:8 light dark regime and fed adlibidum with lettuce and a variety of other vegetables.
Staging and preparation of embryos of L. stagnalis
Freshly deposited egg masses were collected and their development monitored. Following the first cleavage, egg masses were cultured in snail water  at 25°C. All stages are indicated in hours post first cleavage (hpfc) and days post first cleavage (dpfc). At the desired developmental time point individual egg capsules were removed from an egg mass and freed from the jelly by rolling them over moist filter paper. Embryos were manually dissected from their capsules using forceps and needles and fixed according to the subsequent experimental procedure (see below).
Confocal laser scanning microscopy (CLSM)
29 embryonic stages between 27 and 87 hpfc were fixed at intervals of one to five hours. For each developmental stage, 29 to 126 individuals were visualised, and on average 6 individuals were imaged. To account for fixation artefacts several fixation treatments were tested on embryos between 27 and 37 hpfc, ranging from no fixation to extended fixations overnight at room temperature and in varying amounts of gluteraldehyde in combination with a paraformaldehyde-based fixation. Fixation with 4% paraformaldehyde (PFA) in 1X phosphate buffered saline (PBS) for one hour at room temperature, or overnight at 4°C, was found to be optimal. Fixed specimens were washed three times in PBS and processed immediately or stored at 4°C for up to five weeks. For cytoplasmic and nuclear staining samples were incubated in a 1/1000 dilution of Sytox Orange (Molecular probes, S11368) in PBS with 0.1% TritonX for two hours at room temperature. Samples were then washed three times in PBS, dehydrated through a graded ethanol series and embedded in a 1:2 mixture of benzyl benzoate and benzyl alcohol (BB:BA). Optical sections were captured using a Zeiss LSM 510 Meta with the following settings: HeNe 543 laser at a power of 2.9%; pinhole between 50 μm and 60 μm (0.94 to 1.13 Airy Units); amplifier gain of 1; amplifier offset and gain adjusted to the sample brightness; stack size 1024 x 1024 with a stack thickness between 0.81 μm and 0.9 μm; scan speed and number of scans 7 and 4 or 6 and 8 respectively. For individual images the stack size was 2048 x 2048 with a scan speed and number of 6 and 8 respectively. All images were false-coloured and adjusted for brightness using Macnification version 2.0.1.
Scanning electron microscopy
Between 55 and 278 embryos for each time point from 27 to 67 hpfc at five hour intervals were fixed in 2.5% gluteraldehyde in PBS at 4°C overnight. These were then dehydrated through a graded ethanol series and dried overnight in hexamethyldisilazane. Samples were mounted on carbon pads on aluminium stubs and sputter-coated with a gold-palladium alloy before being imaged with a scanning electron microscope at 3.8 kV. All SEM images were edited in Adobe Photoshop CS3 version 10.0.1 by applying the ‘auto levels’ and ‘auto contrast’ functions.
Histology and Histochemistry
The endogenous alkaline phosphatase (AP) activity of 13 developmental stages ranging from 37 to 117 hpfc at 3 to 5 hour intervals was examined. Between 34 and 154 individuals were included in each experiment. Additionally, 14 older larvae (ranging from five days post first cleavage until hatching from the egg capsule) were also assayed for AP activity. For each developmental stage, images of three to 19 individuals were captured. Embryos were fixed for 45 to 60 min in 4% PFA in 1X PBS containing 0.1% Tween20 (PBTw), and rinsed in 1X PBS before being incubated in AP reaction buffer (100 mM Tris, 100 mM NaCl, pH 9.5) for 5 to 20 min. AP reaction buffer was replaced by detection buffer (AP reaction buffer, 50 mM MgCl2, 175 μg/mL BCIP and 450 μg/mL NBT). The colour reaction was stopped after 15 to 60 min at an optimal signal to background ratio by replacing the detection buffer with 0.1 M Glycine pH 2 containing 0.1% Tween20. Samples were then rinsed in PBS and post-fixed overnight at room temperature in 4% PFA in PBS, dehydrated through a graded ethanol series, embedded in BB:BA and viewed and photographed using a Zeiss microscope Axio Imager Z1. A fraction of larger, older (5+ dpfc) larvae were washed twice in PBTw following fixation, and then embedded in 60% glycerol and imaged under a Zeiss stereo microscope discovery V8.
For developmental stages between 47 hpfc and 5+ dpfc, the endogenous peroxidase (PO) activity of 45 to 139 individuals was examined prior to performing the AP assay (described above) in order to visualise the activity of both enzymes at once. Samples fixed as described above were first rinsed twice in 50 mM Tris pH 7.3, and then pre-incubated in 50 mM Tris pH 7.3 containing 1 mg/mL diaminobenzidine (DAB) for 15 to 20 min before supplementing the solution with a 1/3000 dilution of 30% hydrogen peroxide. The colour reaction was monitored and stopped (usually after one to two minutes) by rinsing the samples for about 10 min in 1X PBS. The AP assay (as described above) was then performed on this material. One to 13 individuals per developmental stage were photo-documented.
The overall shape of the early 29 to 32 hpfc archenteron is slit-like (Figures 1B’ and 2B, C). Between 34 and 37 hpfc the blastopore opening narrows, and the archenteron develops a large round lumen (Figures 1C’ and 2D, E). In most embryos at this stage, a variable number of cells at the tip of the archenteron are in contact with dorsal ectodermal cells directly beneath the large head vesicle cells. By 37 hpfc the contact between endoderm and dorsal ectoderm appears to be firmly established (Figure 2F). This is the only region in the embryo where these two cell layers are in direct contact with each other, the archenteron is otherwise bordered by mesodermal cells or intercellular spaces. At this stage, neither the ectodermal nor the endodermal cells at the contact site display an altered cell morphology compared with their neighbours using Sytox Orange.
The first signs of differentiation of the dorsal ectoderm cells as observable by CSLM occur at 39 hpfc. At this stage, these cells take on a columnar morphology and are clearly distinguishable from adjacent ectoderm cells (Figure 2G). The columnar cells are in direct contact with four to five cells of the tip of the underlying archenteron. These endodermal cells in turn are characterised by a lack of large vacuoles that are present in adjacent cells of the archenteron (indicated by ‘x”s in Figure 2G). For this reason these archenteron-tip cells have been referred to as “small-celled entoderm” , here as small celled endoderm. The number of endodermal cells contacting presumptive shell gland cells remains low during the period of contact, never exceeding six cells. During the next hours the morphological differentiation of both cell layers becomes more pronounced with the nuclei of presumptive shell forming cells assuming a basal location (Figure 2I-K).
The relative arrangement of PO and AP activity domains persists from 77 hpfc to 117 hpfc. The centre of the shell field displays AP activity with increasing intensity towards the shell field margin (Figure 5C, C’, D”). During the following stages AP activity in the centre of the shell field gradually decreases (Figure 5C, D). At 117 hpfc AP activity is found in a line of cells proximal to the shell field margin (Figure 5D). At this stage the secreted organic material and the highly elongated cells of the shell field margin continue to exhibit a strong PO activity (Figure 5C”’ and D”’).
In the periphery of the PO positive shell field margin, a faint ring of AP+ cells is detectable from 72 hpfc on (Figure 6). This signal possibly represents the AP+ domain of non-invaginated cells seen in earlier stages (see white arrows in Figures 3 and 4). During the course of shell field differentiation, the activities of both enzymes are continuously located in adjacent, non-overlapping cell populations within the shell field (Figure 6A-C”’; see Figure 8 for a schematic summary of these observations).
Non-shell related AP and PO activities during larval development
In various molluscan groups, the initial differentiation of the dorsal shell forming ectoderm has been observed to coincide with the presence of a tight contact with underlying endodermal cells (reviewed in ). These observations raised the possibility that this contact is required for the specification of molluscan shell forming cells in general. Based on manipulative experiments, first Raven  and later Hess [34, 35] concluded that it is this dorsal ectoderm/endoderm contact that specifies the shell field. Raven differentiates between two possibilities of contact-dependent shell field specification, induction vs. activation. Raven  realised that if the dorsal ectoderm is truly induced to become the shell gland by such a contact (rather than activated as would be the case if a population of dorsal ectodermal cells were already specified in someway), two morphogenic preconditions must be realised. Firstly, only a restricted part of the endoderm (i.e. cells at the tip of the archenteron) should be able to elicit this specification in the overlying ectoderm. Secondly, the whole ectoderm (or at least the majority) should be able to respond to this induction by forming a shell gland. Raven’s observations based on four embryos (whose gastrulation had been perturbed by lithium and which developed an ectopic shell gland) lead him to conclude that most of the ectoderm is indeed able to respond to signals from the underlying endoderm, and that therefore the dorsal ectoderm is truly induced by the endoderm to become shell forming tissue, rather than activated. This model of induction-mediated shell field specification has since been supported , modified [13, 35] and contradicted [36–38]. These studies report a wide capacity of the ectoderm to form a shell field, but disagree about the origin of the “inductive cue”. Hess’s observations of partial embryos after blastomere separation in Bythinia and L. stagnalis[34, 35] support the contact dependent model of shell field specification, but indicate that any endodermal tissue, even single cells, is capable of induction. Cell deletion experiments in Ilyanassa support the hypothesis that there is no cellular specificity in the inducing endoderm: all combinations of ectoderm and endoderm can generate a shell field. Furthermore, in Ilyanassa it has been shown that the tip of the archenteron is never in close proximity to the dorsal ectoderm . Labordus and van der Wal  extending the studies on Ilyanassa by Clement  and Cather , suggest a scenario which distinguishes between the histogenic and morphogenic differentiation of the shell gland. Based on observations of misdeveloped embryos producing internal shell material, Labordus and van der Wal  propose that the histogenic differentiation necessary to produce such material is independent of inductive interactions, whereas the correct spatial organisation of shell forming tissues depends on spatially correct inductive interactions between the D-quadrant macromeres and the overlying micromeres earlier in development. Based on that study, McCain  conducted cell deletion experiments that suggest inductive interactions among the micromeres are also required to give rise to the larval shell forming tissues. The disturbance of these interactions by the removal of participating cells leads to the internal deposition of calcium carbonate similar to those observed by earlier workers, supporting the assumption that the processes leading to the histogenetic vs. the morphogenetic differentiation of larval shell forming tissues do not depend on each other. This hypothesis is further corroborated by work in experimental systems that allow for an artificially induced shell internalisation, e.g. by exposure to environmental toxins such as platinum [40, 41]. In these systems (Marisa cornuarietis and Planorbis corneus), platinum interferes with the localisation of shell material and the growth of shell forming tissues, while the cellular differentiation of these tissues appears to remain unaffected [40, 41].
While Raven’s hypothesis of induction-mediated shell gland specification still represents the most comprehensive theory of how the future shell forming cells are initially specified in molluscs, contradictory observations have been reported for a number of disparate taxa. In the pulmonate taxa Bradybaena and Achatina marginata the shell field is differentiated before any contact with the underlying endoderm is established, in the Caenogastropod Marisa this contact is interrupted by intermingled cells, and in other gastropod species (Ilyanassa obsoleta and Achatina fulica) as well as bivalves (Cyclas and Sphaerium) no contact is present (reviewed in ). Unfortunately, none of these previous studies utilised high resolution imaging techniques such as CLSM that are available today, or conducted their investigations with high temporal resolution. Nonetheless we must acknowledge that there does exist the possibility of an alternative, contact-independent shell gland specification mechanism, leaving open the question as to whether the dorsal ectoderm/endoderm contact event represents the ancestral molluscan mode of shell gland specification.
While the present study was not intended to clarify the molecular mechanisms of shell gland specification, nor to differentiate between scenarios of induction vs. activation as proposed by Raven , it does clarify the nature of the cellular interactions between endoderm and ectoderm prior to and during shell gland specification, and also provides an accurate framework for the timing of these events in L. stagnalis at 25°C. Using CSLM we could reconstruct the cellular arrangements and movements during contact between dorsal ectoderm and endoderm. Despite its importance, former studies do not include a description of how this contact is initially established. If, as Raven  proposes, the ‘small-celled endoderm’ truly induces the overlying dorsal ectoderm in Lymnaea, these endodermal cells should have acquired their inductive capacity prior to contact. Such prior differentiation is not revealed by Sytox Orange staining in our study (both dorsal ectoderm and the ‘small-celled endoderm’ show the first signs of differentiation after contact establishment; see Figure 2F and G), nor by Raven using standard histological stains . Raven concluded that acquisition of an inductive capacity by the endoderm is not revealed by any histological differentiation. Indeed, a molecular differentiation of the contacting endoderm could be expected to precede any visible histological differentiation. Identification of such molecular markers would provide great insight into the evolution of the molluscan shell.
Our study also reveals a pronounced bilateral organisation of early shell gland development; the invagination of the shell gland begins when two lateral points of the thickened dorsal ectoderm form two lateral depressions (Figure 1D-E’, 2J-O). This bilateral organisation persists until the margins of the shell gland converge above the lumen of the invaginated shell gland and the bifurcated lumen rounds up (Figures 1F’, 2P-R). The formation of this shell gland lumen coincides with the secretion of the first insoluble shell material. None of the invaginated shell gland cells appear to participate in the secretion of this first water insoluble material which emerges from the peripheral non-invaginated shell gland cells  (Figure 1F’). This observation has raised the hypothesis that the process of shell gland invagination is required in order to bring cells at the periphery of the shell gland into close contact, and to thereby initiate the secretion of an insoluble shell forming matrix without a central hole above the shell gland lumen [42, 43]. Shortly afterwards, the first signs of asymmetry in the shell gland appear. The invaginated part of the shell gland shifts to the left side which generates a larger distance between the centre of the lumen and the peripheral secreting cells on the right side than on the left side (Figures 1H’ , 4C” , C”’). This early asymmetry presumably reflects the future coiling direction of the mature shell.
While shell gland formation is a deeply conserved feature of molluscan development, there is considerable diversity in its ontogeny within and between all molluscan groups. For those species with internal or reduced shells, the formation and further differentiation of the shell gland differs from that seen in L. stagnalis and other externally shelled molluscs (reviewed in ). In shell-less cephalopods for example, shell gland development ceases during dorsal ectoderm invagination, and an evaginated shell field never forms. In cephalopods with an internal shell, the shell gland is internalised and characterised by a closed pore, and is therefore referred to as a “shell sac”. This structure is not thought to be formed by an invagination of the central part of the thickened dorsal ectoderm. Instead, the peripheral cells of the thickened dorsal ectoderm bulge upwards and overgrow the central cells. An internalised shell gland or “shell sac” is also found in shell-less terrestrial slugs, but is formed by a different mechanism. Here, the dorsal ectoderm invaginates as it does in shelled gastropods, but continues inwards leading to a complete internalisation of all shell gland cells, and consequently a closure of the shell gland. These ontogenetic events in secondarily shell-less slugs also illustrate their common ancestry with shelled snails such as Lymnaea.
Endogenous enzyme activities as a tool to illustrate larval development
This work represents a platform from which analyses aimed at the identification of the molecular regulators responsible for shell development in L. stagnalis can be conducted. We have described the timing of developmental events critical to specification of shell forming cells, and the movements of cells that take part in these processes. We also highlight the use of histochemical assays that allow for the detection of endogenous alkaline phosphatase and peroxidase activity within shell forming cells. Understanding the molecular basis of shell development from a range of molluscan representatives will provide deep insight into the evolutionary events that supported the generation of much of today’s molluscan diversity. The work presented here is a first step towards the development of L. stagnalis as a model to understand how this diversity arose.
JH carried out the experimental procedures. DJJ conceived and supervised the study. Both authors participated in the design of the study and drafted the manuscript. Both authors read and approved the final manuscript.
We gratefully acknowledge Luciana Macis for technical assistance and maintenance of snail lines, and Dorothea Hause-Reitner for capturing the SEM images. Nora Glaubrecht assisted with initial Sytox Orange CLSM experiments. This work was supported by Deutsche Forschungsgemeinschaft (DFG) funding to DJJ through the CRC for Geobiology and the German Excellence Initiative, and DFG project number JA 2108/1-1.
- Ponder WF, Lindberg DR: Phylogeny and Evolution of the Mollusca. 2008, Berkeley: University of California PressView ArticleGoogle Scholar
- Brusca RC, Brusca GJ: Invertebrates. 2002, Sunderland: Sinauer Associates IncorporatedGoogle Scholar
- Lowenstam HA, Weiner S: On biomineralization. 1989, New York: Oxford University Press, IncGoogle Scholar
- Comfort A: The pigmentation of molluscan shells. Biol Rev. 1951, 26: 285-301.View ArticleGoogle Scholar
- Meinhardt H: The Algorhithmic Beauty of Sea Shells. 2009, Berlin Heidelberg: SpringerView ArticleGoogle Scholar
- Abbott RT, Dance SP: Compendium of Seashells: a Full-color Guide to More Than 4,200 of the World’s Marine Shells. 1998, El Cajon: Odyssey PublishingGoogle Scholar
- Marin F, Luquet G, Marie B, Medakovic D: Molluscan shell proteins: primary structure, origin, and evolution. Curr Top Dev Biol. 2007, 80: 209-276.View ArticleGoogle Scholar
- Jackson DJ, McDougall C, Woodcroft B, Moase P, Rose RA, Kube M, Reinhardt R, Rokhsar DS, Montagnani C, Joubert C, Piquemal D, Degnan BM: Parallel Evolution of Nacre Building Gene Sets in Molluscs. Mol Biol Evol. 2010, 27: 591-608. 10.1093/molbev/msp278.View ArticlePubMedGoogle Scholar
- Marie B, Le-Roy N, Zanella-Cléon I, Becchi M, Marin F: Molecular evolution of mollusc shell proteins: insights from proteomic analysis of the edible mussel Mytilus. J Mol Evol. 2011, 72: 531-546. 10.1007/s00239-011-9451-6.View ArticlePubMedGoogle Scholar
- Marie B, Jackson DJ, Ramos-Silva P, Zanella-Cléon I, Guichard N, Marin F: The shell-forming proteome of Lottia gigantea reveals both deep conservations and lineage-specific novelties. FEBS J. 2013, 280: 214-232. 10.1111/febs.12062.View ArticlePubMedGoogle Scholar
- Kniprath E: Ontogeny of the Molluscan Shell Field: a Review. Zool Script. 1981, 10: 61-79. 10.1111/j.1463-6409.1981.tb00485.x.View ArticleGoogle Scholar
- Haszprunar G, von-Salvini-Plawen L, Rieger RM: Larval planktotrophy - a primitive trait in the Bilateria?. Acta Zool. 1995, 76: 141-154. 10.1111/j.1463-6395.1995.tb00988.x.View ArticleGoogle Scholar
- Cather JN: Cellular Interactions in the Development of the Shell Gland of the Gastropod, Ilyanassa. J Exp Zool. 1967, 166: 205-223. 10.1002/jez.1401660204.View ArticlePubMedGoogle Scholar
- Hejnol A, Martindale MQ, Henry JQ: High-resolution fate map of the snail Crepidula fornicata: The origins of ciliary bands, nervous system, and muscular elements. Dev Biol. 2007, 305: 63-76. 10.1016/j.ydbio.2007.01.044.View ArticlePubMedGoogle Scholar
- Jackson DJ, Ellemor N, Degnan BM: Correlating gene expression with larval competence, and the effect of age and parentage on metamorphosis in the tropical abalone Haliotis asinina. Mar Biol. 2005, 147: 681-697. 10.1007/s00227-005-1603-z.View ArticleGoogle Scholar
- Jackson DJ, Wörheide G, Degnan BM: Dynamic expression of ancient and novel molluscan shell genes during ecological transitions. BMC Evol Biol. 2007, 7: 160-10.1186/1471-2148-7-160.PubMed CentralView ArticlePubMedGoogle Scholar
- Timmermans LPM: Studies on shell formation in molluscs. Neth. J Zool. 1969, 19: 63-78.Google Scholar
- Jacobs DK, Wray CG, Wedeen CJ, Kostriken R, DeSalle R, Staton JL, Gates RD, Lindberg DR: Molluscan engrailed expression, serial organization, and shell evolution. Evol Dev. 2000, 2: 340-347. 10.1046/j.1525-142x.2000.00077.x.View ArticlePubMedGoogle Scholar
- Wanninger A, Haszprunar G: The expression of an engrailed protein during embryonic shell formation of the tusk-shell, Antalis entalis (Mollusca, Scaphopoda). Evol Dev. 2001, 3: 312-321. 10.1046/j.1525-142X.2001.01034.x.View ArticlePubMedGoogle Scholar
- Nederbragt AJ, van-Loon AE, Dictus WJAG: Expression of Patella vulgata orthologs of engrailed and dpp-BMP2/4 in adjacent domains during molluscan shell development suggests a conserved compartment boundary mechanism. Dev Biol. 2002, 246: 341-355. 10.1006/dbio.2002.0653.View ArticlePubMedGoogle Scholar
- Hinman VF, O’Brien EK, Richards GS, Degnan BM: Expression of anterior Hox genes during larval development of the gastropod Haliotis asinina. Evol Dev. 2003, 5: 508-521. 10.1046/j.1525-142X.2003.03056.x.View ArticlePubMedGoogle Scholar
- Iijima M, Takeuchi T, Sarashina I, Endo K: Expression patterns of engrailed and dpp in the gastropod Lymnaea stagnalis. Dev Genes Evol. 2008, 218: 237-251. 10.1007/s00427-008-0217-0.View ArticlePubMedGoogle Scholar
- Kin K, Kakoi S, Wada H: A novel role for dpp in the shaping of bivalve shells revealed in a conserved molluscan developmental program. Dev Biol. 2009, 329: 125-166.View ArticleGoogle Scholar
- Samadi L, Steiner G: Involvement of Hox genes in shell morphogenesis in the encapsulated development of a top shell gastropod (Gibbula varia L.). Dev Gen Evol. 2009, 219: 523-530. 10.1007/s00427-009-0308-6.View ArticleGoogle Scholar
- Hashimoto N, Kurita Y, Wada H: Developmental role of dpp in the gastropod shell plate and co-option of the dpp signaling pathway in the evolution of the operculum. Dev Biol. 2012, 366: 367-37. 10.1016/j.ydbio.2012.04.010.View ArticlePubMedGoogle Scholar
- Raven CP: Morphogenesis in Limnaea stagnalis and its disturbance by lithium. J Exp Zool. 1952, 121: 1-77. 10.1002/jez.1401210102.View ArticleGoogle Scholar
- Kniprath E: Zur Ontogenese des Schalenfeldes von Lymnaea stagnalis. Dev Gen Evol. 1977, 181: 11-30.Google Scholar
- Raven CP: The Development of the Egg of Limnaea Stagnalis L. From the First Cleavage Till the Trochophore Stage, With Special Reference To Its‘ Chemical Embryology’. Arch Neer Zool. 1946, 7: 353-434.Google Scholar
- Wassnig M, Southgate PC: Embryonic and larval development of Pteria penguin (Röding, 1798)(Bivalvia: Pteriidae). J Moll Stud. 2012, 78: 134-141. 10.1093/mollus/eyr051.View ArticleGoogle Scholar
- Bielefeld U, Becker W: Embryonic development of the shell in Biomphalaria glabrata (Say). Int J Dev Biol. 1991, 35: 121-131.PubMedGoogle Scholar
- Shimizu K, Sarashina I, Kagi H, Endo K: Possible functions of Dpp in gastropod shell formation and shell coiling. Dev Genes Evol. 2011, 221: 59-68. 10.1007/s00427-011-0358-4.View ArticlePubMedGoogle Scholar
- Thomas JD, Lough AS, Lodge RW: The Chemical Ecology of Biomphalaria glabrata (Say), the Snail Host of Schistosoma mansoni Sambon: The Search for Factors in Media Conditioned by Snails which Inhibit their Growth and Reproduction. J Anat. 1975, 12: 421-436.Google Scholar
- Morrill JB: Development of the Pulmonate Gastropod, Lymnaea. Developmental Biology of Freshwater Invertebrates. Edited by: Harrison FW, Cowden RR. 1982, New York: Alan R. Liss, Inc, 399-483.Google Scholar
- Hess O: Die Entwicklung von Exogastrulakeimen bei dem Süsswasser-Prosobranchier Bithynia tentaculata L. Dev Gen Evol. 1956, 148: 474-488.Google Scholar
- Hess O: Die Entwicklung von Halbkeimen bei dem Süsswasserpulmonaten Limnaea stagnalis L. Dev Gen Evol. 1957, 150: 124-145.Google Scholar
- Clement AC: Development of Ilyanassa following removal of the D macromere at successive cleavage stages. J Exp Zool. 1962, 149: 193-215. 10.1002/jez.1401490304.View ArticleGoogle Scholar
- Collier JR, McCann-Collier M: Shell gland formation in the Ilyanassa embryo. Exp Cell Res. 1964, 34: 512-514. 10.1016/0014-4827(64)90236-8.View ArticlePubMedGoogle Scholar
- Labordus V, van der-Wal UP: The determination of the shell field cells during the first hour in the sixth cleavage cycle of eggs of Ilyanassa obsoleta. J Exp Zool. 1986, 239: 65-75. 10.1002/jez.1402390109.View ArticleGoogle Scholar
- McCain ER: Cell interactions influence the pattern of biomineralization in the Ilyanassa obsoleta (Mollusca) embryo. Dev Dyn. 1992, 195: 188-200. 10.1002/aja.1001950305.View ArticlePubMedGoogle Scholar
- Osterauer R, Marschner L, Betz O, Gerberding M, Sawasdee B, Cloetens P, Haus N, Sures B, Triebskorn R, Köhler H: Turning snails into slugs: induced body plan changes and formation of an internal shell. Evol Dev. 2010, 12: 474-483. 10.1111/j.1525-142X.2010.00433.x.View ArticlePubMedGoogle Scholar
- Marschner L, Triebskorn R, Köhler H: Arresting mantle formation and redirecting embryonic shell gland tissue by platinum2+ leads to body plan modifications in Marisa cornuarietis (Gastropoda, Ampullariidae). J Morphol. 2012, 273: 830-841. 10.1002/jmor.20019.View ArticlePubMedGoogle Scholar
- Kniprath E: The functional morphology of the embryonic shell-gland in the conchiferous molluscs. Malacologia. 1979, 18: 549-552.Google Scholar
- Eyster LS: Ultrastructure of early embryonic shell formation in the opisthobranch gastropod Aeolidia papillosa. Biol Bull. 1983, 165: 394-408. 10.2307/1541204.View ArticleGoogle Scholar
- Hessle L, Johnson KA, Anderson HC, Narisawa S, Sali A, Goding JW, Terkeltaub R, Millán JL: Tissue-nonspecific alkaline phosphatase and plasma cell membrane glycoprotein-1 are central antagonistic regulators of bone mineralization. Proc Natl Acad Sci U S A. 2002, 99: 9445-9449. 10.1073/pnas.142063399.PubMed CentralView ArticlePubMedGoogle Scholar
- Harmey D, Hessle L, Narisawa S, Johnson KA, Terkeltaub R, Millán JL: Concerted Regulation of Inorganic Pyrophosphate and Osteopontin by Akp2, Enpp1, and Ank: An Integrated Model of the Pathogenesis of Mineralization Disorders. Am J Pathol. 2004, 164: 1199-1209. 10.1016/S0002-9440(10)63208-7.PubMed CentralView ArticlePubMedGoogle Scholar
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.