Development of the musculature in the limpet Patella (Mollusca, Patellogastropoda)

 Whole-mount technique using fluorescent-labelled phalloidin for actin staining and confocal laser scanning microscopy as well as semi-thin serial sectioning, scanning and transmission electron microscopy were applied to investigate the ontogeny of the various muscular systems during larval development in the limpets Patella vulgata L. and P. caerulea L. In contrast to earlier studies, which described a single or two larval shell muscles, the pretorsional trochophore-like larva shows no less than four different muscle systems, namely the asymmetrical main head/foot larval retractor muscle, an accessory larval retractor with distinct insertion area, a circular prototroch/velar system, and a plexus-like pedal muscle system. In both Patella species only posttorsional larvae are able to retract into the shell and to close the aperture by means of the operculum. Shortly after torsion the two adult shell muscles originate independently in lateral positions, starting with two fine muscle fibres which insert at the operculum and laterally at the shell. During late larval development the main larval retractor and the accessory larval retractor become reduced and the velar muscle system is shed. In contrast, the paired adult shell muscles and the pedal muscle plexus increase in volume, and a new mantle musculature, the tentacular muscle system, and the buccal musculature arise. Because the adult shell muscles are entirely independent from the various larval muscular systems, several current hypotheses on the ontogeny and phylogeny of the early gastropod muscle system have to be reconsidered. Received: 23 June 1998 / Accepted: 25 November 1998     

Ontogenetic torsion in two basal gastropods occurs without shell attachments for larval retractor muscles

Results of this study on two species of vetigastropods contradict the long-standing hypothesis, originally proposed by Garstang (1929), that the larval retractor muscles power the morphogenetic movement of ontogenetic torsion in all basal gastropods. In the trochid Calliostoma ligatum and the keyhole limpet Diodora aspera, the main and accessory larval retractor muscles failed to establish attachments onto the protoconch (larval shell) when the antibiotics streptomycin sulfate and penicillin G were added to cultures soon after fertilization. Defects in protoconch mineralization were also observed. Despite these abnormalities, developing larvae of these species accomplished complete or almost complete ontogenetic torsion, a process in which the head and foot rotate by 180 degrees relative to the protoconch and visceral mass. Analysis by using phalloidin-fluorophore conjugate and transmission electron microscopy showed that myofilaments differentiated within myocytes of the larval retractor muscles and adherens-like junctions formed between muscle and mantle epithelial cells in both normal and abnormal larvae. However, in abnormal larvae, apical microvilli of mantle cells that were connected to the base of the larval retractor muscles failed to associate with an extracellular matrix that normally anchors the microvilli to the mineralized protoconch. If morphogenesis among extant, basal gastropods preserves the original developmental alteration that created gastropod torsion, as proposed by Garstang (1929), then the alteration involved something other than the larval retractor muscles. Alternatively, the developmental process of torsion has evolved subsequent to its origin in at least some basal gastropod clades so that the original alteration is no longer preserved in these clades.     

Larval muscle contraction fails to produce torsion in a trochoidean gastropod.

The causes and effects of ontogenetic torsion in gastropods have been debated intensely for more than a century (1-19). Occurring rapidly and very early in development, torsion figures prominently in shaping both the larval and adult body plans. We show that mechanical explanations of the ontogenetic event that invoke contraction of larval retractor muscles are inadequate to explain the observed consequences in some gastropods. The classic mechanical explanation of Crofts (4, 5) and subsequent refinements of her explanation have been based on species with rigid larval shell properties (18, 19) that cannot be extrapolated to all gastropods. We present visual evidence of the lack of rigidity of the uncalcified larval shell in a basal trochid gastropod, Margarites pupillus (Gould), and provide photographic confirmation of our prediction that larval retractor muscle contraction is insufficient to produce more than local deformation or dimpling at the site of muscle insertion. These findings do not refute muscular contraction as a primary cause of ontogenetic torsion in gastropods that calcify their larval shells prior to the onset of torsion, nor do they refute the monophyly of torsion. They do, however, suggest that torsion may be a loosely constrained developmental process with multiple pathways to the more constrained end result (20, 21).     

Major muscle systems in the larval caenogastropod,Ilyanassa obsoleta,display different patterns of development

This study describes the anatomical and developmental aspects of muscular development from the early embryo to competent larval stage in the gastropod Ilyanassa obsoleta. Staining of F‐actin revealed differential spatial and temporal patterns of several muscles. In particular, two major muscles, the larval retractor and pedal retractor muscles originate independently and display distinct developmental patterns similar to observations in other gastropod species. Additionally, together with the larval retractor muscle, the accessory larval muscle developed in the embryo at the trochophore stage. Therefore, both these muscles develop prior to ontogenetic torsion. The pedal retractor muscle marked the most abundant growth in the mid veliger stage. Also during the middle stage, the metapodial retractor muscle and opercular retractor muscle grew concurrently with development of the foot. We show evidence that juvenile muscles, such as the buccal mass muscle and siphon muscle develop initially during the late veliger stage. Collectively, these findings substantiate that larval myogenesis involves a complex sequence of events that appear evolutionary conserved within the gastropods, and set the stage for future studies using this model species to address issues concerning the evolution and eventual fates of larval musculature in molluscs. J. Morphol., 2009. © 2009 Wiley‐Liss, Inc.     

Modern insights on gastropod development: Reevaluation of the evolution of a novel body plan

More than a century of speculation about the evolutionary originof the contorted gastropod body plan has been inspired by adultanatomy and by long-standing developmental observations. Theresult has been a concept of gastropod torsion that I call the"rotation hypothesis." Under the rotation hypothesis, gastropodsoriginated when all components of the visceropallium (shell,mantle, mantle cavity with contained structures, and viscera)rotated by 180° relative to the head and foot. This evolutionaryrotation is echoed during early development of patellogastropodsand vetigastropods and occurs to some extent during developmentof more derived clades. However, comparative developmental dataon ontogenetic torsion are minimal and I argue that the rotationhypothesis is a tautological argument. More recent studies onrepresentatives from 3 major clades of gastropods suggest thatthe highly conserved aspect of gastropod development is notsynchronous rotation of all components of the visceropalliumrelative to the head and foot but rather a state of anatomicalorganization in which the developing mantle cavity is on theright but the shell coil is posterior (endogastric orientation).This conserved state of developmental anatomy has inspired analternative hypothesis for the evolutionary origin of the gastropodbody plan, the "asymmetry hypothesis." Under the asymmetry hypothesis,the gastropod mantle cavity originated from 1 side only of abilateral set of mantle cavities. The asymmetry hypothesis doesnot require a saltation event to explain the origin of gastropods,nor does it require that the ancient molluscan precursor ofgastropods carried the shell coil over the head (exogastricorientation).     

Molluscan Metamorphosis: A Study in Tissue Transformation

Metamorphosis of the pelagic larvae of benthic marine invertebratesis often a cataclysmic event in which a rapid loss of organsspecialized for larval life occurs simultaneously with the renewalor increased rate of development of potential adult organs.In the nudibranch gastropod Phestilla sibogae this change involvesloss of the velum, shell, operculum, larval kidney, some retractormuscles, and some of the pedal mucous glands. Exit from thelarval shell at metamorphosis is rapid and is correlated withthe spread of epidermis from the larval foot over the visceralmass as the visceral mass emerges from the shell aperature.This spreading of epipodial epidermis to cover the entire bodyhas not been previously reported for other nudibranchs. Neithercell proliferation nor active cell motility are responsiblefor this epidermal migration. Rather it appears that the actionof larval muscles pulls the visceral organs out of the shelland simultaneously causes the epipodial epidermis to cover thevisceral mass. This epidermis becomes the definitive adult epidermis.     

Sequential developmental programmes for retractor muscles of a caenogastropod: reappraisal of evolutionary homologues

Evolutionary changes in the development of shell-attached retractor muscles in gastropods are of fundamental importance to theories about the early evolution and subsequent diversification of this molluscan class. Development of the shell-attached retractor muscle (columellar muscle) in a caenogastropod has been studied at the ultrastructural level to test the hypothesis of homology with the post-torsional left retractor muscle (larval velar retractor) in vetigastropod larvae. The vetigastropod muscle has been implicated in the generation of ontogenetic torsion, a morphogenetic twist between body regions that is important to theories about early gastropod evolution. Two shell-attached retractor muscles develop sequentially in the caenogastropod, Polinices lewisii, which is a pattern that has been also identified in previous ultrastructural studies on a vetigastropod and several nudibranch gastropods. The pattern may be a basal and conserved characteristic of gastropods. I found that the first-formed retractor in larvae of P. lewisii is comparable to the larval velar retractor that exists at the time of ontogenetic torsion in the vetigastropod, Haliotis kamtschatkana. However, the post-metamorphic columellar muscle of P. lewisii is derived exclusively from part of the second-formed muscle, which is comparable to the second-formed pedal muscle system in the vetigastropod. I conclude that the post-metamorphic columellar muscle of P. lewisii, is not homologous to the larval velar retractor of the vetigastropod, H. kamtschatkana.     

Myogenesis in Aplysia californica (Cooper, 1863) (Mollusca,Gastropoda, Opisthobranchia) with special focus on muscular remodeling during metamorphosis

To date only few comparative approaches tried to reconstruct the ontogeny of the musculature in invertebrates. This may be due to the difficulties involved in reconstructing three dimensionally arranged muscle systems by means of classical histological techniques combined with light or transmission electron microscopy. Within the scope of the present study we investigated the myogenesis of premetamorphic, metamorphic, and juvenile developmental stages of the anaspidean opisthobranch Aplysia californica using fluorescence F‐actin‐labeling in conjunction with modern confocal laser scanning microscopy. We categorized muscles with respect to their differentiation and degeneration and found three true larval muscles that differentiate during the embryonic and veliger phase and degenerate during or slightly after metamorphosis. These are the larval retractor, the accessory larval retractor, and the metapodial retractor muscle. While the pedal retractor muscle, some transversal mantle fibers and major portions of the cephalopedal musculature are continued and elaborated during juvenile and adult life, the buccal musculature and the anterior retractor muscle constitute juvenile/adult muscles which differentiate during or after metamorphosis. The metapodial retractor muscle has never been reported for any other gastropod taxon. Our findings indicate that the late veliger larva of A. californica shares some common traits with veligers of other gastropods, such as a larval retractor muscle. However, the postmetamorphic stages exhibit only few congruencies with other gastropod taxa investigated to date, which is probably due to common larval but different adult life styles within gastropods. Accordingly, this study provides further evidence for morphological plasticity in gastropod myogenesis and stresses the importance of ontogenetic approaches to understand adult conditions and life history patterns. J. Morphol., 2008. © 2007 Wiley‐Liss, Inc.     

Early differentiating neuron in larval abalone (Haliotis kamtschatkana) reveals the relationship between ontogenetic torsion and crossing of the pleurovisceral nerve cords

Crossing of the pleurovisceral nerve cords in gastropods has supported the view that gastropods evolved by 180 degrees rotation between the ventral and dorsal body regions. Indeed, a rotation of this type occurs as a dramatic morphogenetic movement ("ontogenetic torsion") during the development of basal gastropods. According to a long-standing hypothesis, ontogenetic torsion in basal gastropods preserves an ancient developmental aberration that generated the contorted gastropod body plan. It follows from this reasoning that crossing of the pleurovisceral nerve cords during gastropod development should be mechanically coupled to ontogenetic torsion. The predicted mechanical coupling can now be examined because of the discovery of an early differentiating neuron in Haliotis kamtschatkana (Vetigastropoda) that expresses 5-hydroxytryptamine-like immunoreactivity. The neuron appeared to delineate the trajectory of the pleurovisceral nerve cords beginning before ontogenetic torsion. Before torsion, the neuronal soma is embedded in mantle epithelium at the ventral midline and two neurites extend anteriorly toward the apical sensory organ. Contrary to expectation, the two neurites of this cell did not cross-over during ontogenetic torsion because the soma of this mantle neuron shifted in the same direction as the rotating head and foot. Full crossing of the pleurovisceral nerve cords occurred gradually during later development as the mantle cavity deepened and expanded leftward. These results are consistent with a generalization emerging from comparative studies indicating a conserved developmental stage for gastropods in which the mantle cavity is localized to one side, despite a fully "post-torsional" orientation for other body components. Developmental morphology before this stage is much more variable among different gastropod clades.     

Ontogenetic Torsion and Protoconch Form in the Archaeogastropod Haliotis kamtschatkana: Evolutionary Implications

Ontogenetic torsion in archaeogastropods has strongly influenced theories about early gastropod evolution, but the seminal studies by Crofts (1937, 1955) remain the major source of information about tissue movements during this developmental process. Computer-generated reconstructions of histological sections indicate that the cephalopodium of Haliotis kamtschatkana Jonas, 1845 rotates by a full 180° relative to the shell and visceral lobe during the first quarter of pre-metamorphic development. However, a portion of pallial epithelium, including some of the shell field, accompanies the rotating cephalopodium; a process facilitated by detachment of the pallium from the apertural rim of the protoconch. Transmission electron microscopy indicates that a tract of the larval retractor muscle, which Crofts (1955) implicated in the mechanism of torsion, inserts on both pedal and pallial cells. A deep invagination of shell field epithelium is a major focus of rotational torque. As a result of pallial deformation during cephalopodial rotation, the anus and gill rudiment are restricted to the right half of the larval body for 2 days after cephalopodial rotation by 180° has been completed. Scanning and transmission electron microscopy indicate that grooves in the lateral flanks of the protoconch correspond to the deep invagination of shell field epithelium. The grooves are not created by a coiling type of accrelionary shell growth or by flexion of the protoconch. A calcareous shelf is secondarily added to the periostracal template of the protoconch along its visceral apertural rim. Morphogenetic movements during ontogenetic torsion in this species are more complex than a simple rotation between cephalopodium and visceropallium and the protoconch shows no evidence of exogastric coiling. © 1997 Published by Elsevier Science Ltd on behalf of The Royal Swedish Academy of Sciences.     

Apical sensory organ in larvae of the patellogastropod Tectura scutum

The apical sensory organ in veliger larvae of a patellogastropod, a basal clade of gastropod molluscs, was studied using ultrastructural and immunohistochemical techniques. Immediately before veligers of Tectura scutum undergo ontogenetic torsion, the apical sensory organ consists of three large cells that generate a very long apical ciliary tuft, two cells that generate a bilateral pair of shorter ciliary tufts, and a neural ganglion (apical ganglion). Putative sensory neurons forming the ganglion give rise to dendrites that extend to the apical surface of the larva and to basal neurites that contribute to a neuropil. The ganglion includes only one ampullary neuron, a distinctive neuronal type found in the apical ganglion of other gastropod veligers. Serotonin immunoreactivity is expressed by a medial and two lateral neurons, all having an apical dendrite, and also by neurites within the neuropil and by peripheral neurites that run beneath the ciliated prototrochal cells that power larval swimming. The three cells generating the long apical ciliary tuft are lost soon after ontogenetic torsion, and the medial serotonergic cell stops expressing serotonin antigenicity in late-stage veligers. The lateral ciliary tuft cells of T. scutum may be homologs of lateral ciliary tuft cells in planktotrophic opisthobranch veligers. A tripartite arrangement of sensory dendrites, as described previously for veligers of other gastropod clades, can be recognized in T. scutum after loss of the apical ciliary tuft cells.     

Development of asymmetry in the caenogastropods Amphissa columbiana and Euspira lewisii

Abstract. The asymmetry displayed by the body plan of gastropods has been directly or indirectly attributed to an evolutionary process called torsion. Torsion is defined as a rotation of 180° between the cephalopodium (head and foot) and visceropallium (visceral organs, mantle, mantle cavity, and shell). During development, the displacement of anatomical components occurs during a process called "ontogenetic torsion." Although ontogenetic torsion is central to theories of gastropod evolution, surprisingly few studies have documented actual tissue movements during the development of asymmetry in gastropods. We investigated the development of the mantle cavity and pleurovisceral nerve connective (visceral nerve loop) in the caenogastropods Amphissa columbiana and Euspira lewisii , because displacements of both of these structures are interpreted as major consequences of torsion. Scanning electron micrographs, histological sections, and immunofluorescence images showed that the developing vis-ceropallium twists by 90° relative to the cephalopodium, the mantle cavity initially forms on the right side, and displacements of the visceral nerve loop become evident on the left side before the right side. A developmental stage in which the mantle cavity is confined to the right side has also been reported in members of the Vetigastropoda and Heterobranchia. We suggest that further comparative studies should test the hypothesis that early development throughout the Gastropoda converges on an embryonic organization in which the mantle cavity and anus are located laterally, despite clade-specific differences in developmental patterns both before and after this stage.     

Reproduction and larval development of the gastropod molluskTegula rustica in Peter the Great Bay, Sea of Japan

The reproduction and larval development of the prosobranch gastropod molluskTegula rustica were studied under laboratory conditions. In Vostok Bay (Peter the Great Bay), the reproduction of theTegula takes place in August, when the water temperature is 19–20°C. Under laboratory conditions, the spawning of females was stimulated by adding a sperm emulsion to a vessel containing adult females. We observed asynchronous and intermittent release of gametes. The egg cell is 190 μm in diameter. Fertilization is external, and the course of development includes a lecithotrophic pelagic larva. Complete development, from fertilization to metamorphosis, takes 7 days in a laboratory culture. The larvae settle when the shell size across the first whorl is 220–230 μm and the total shell whorl is about 90°. The shape of the veliger shell is elongated mitriform and the velum is rounded, made up of a single lobe. The sculpture of the protoconch is irregularly ribbed.     

Behavior,metamorphosis, and muscular organization of the predatory rotifer Acyclus inquietus (Rotifera,Monogononta)

Abstract. The atrochid rotifer, Acyclus inquietus, is a sedentary predator that lives within the colonies of its prey, the rotifer Sinantherina socialis. After larvae infiltrate and become associated with the colony, they secrete a permanent gelatinous tube and undergo metamorphosis to the adult stage. We followed settlement and metamorphosis using bright-field microscopy to document specific larval behaviors after eclosion, and used epifluorescence and confocal microscopy of phalloidin-labeled specimens to visualize some of the morphological changes that occur during metamorphosis. Upon eclosion, larvae possess paired eyespots and a ciliated corona that functions strictly in locomotion. After leaving the parent's gelatinous tube, larvae eventually settle on unoccupied colonies of S. socialis or on other substrates if colonies are unavailable. Settlement involves a period of gliding among colony members before attachment with the foot and the secretion of a gelatinous tube. After settlement, there is a drastic reconfiguration of the corona that involves loss of the eyespots, loss of the coronal cilia, and the formation of the cup-shaped infundibulum, a deep depression in the anterior of the head that leads to the mouth. The development of the infundibulum involves the expansion of tissues around the mouth and is accompanied by a reorientation of the underlying musculature that supplies the infundibulum and allows its use in prey capture. The arrangement of the muscles in the trunk and foot regions, which contain outer circular (complete and incomplete) and inner longitudinal bands, remains unchanged between ontogenetic stages, and reflects the condition characteristic of other rotifers.     

Purification and characterization of a Cys-Gly hydrolase from the gastropod mollusk,Patella caerulea

A magnesium-dependent cysteinyl-glycine hydrolyzing enzyme from the gastropod mollusk Patella caerulea was purified to electrophoretic homogeneity through a simple and rapid purification protocol. The molecular masses of the native protein and the subunit suggest that the enzyme has a homohexameric structure. Structural data in combination with kinetic parameters determined with Cys-Gly and compared with Leu-Gly as a substrate, indicate that the purified enzyme is a member of the peptidase family M17. The finding that an enzyme of the peptidase family M17 is responsible also in mollusks for the breakdown of Cys-Gly confirms the important role of this peptidase family in the glutathione metabolism.     

The influence of temperature on growth rate and length of larval life of the gastropod, Crepidula plana Say

The relationship between rate of larval development and the potential to prolong larval life was examined for larvae of the marine prosobranch gastropod Crepidula plana Say. Larvae were maintained in clean glass dishes at constant temperatures ranging from 12–29°C and fed either Isochrysis galbana Parke (ISO) or a Tahitian strain of Isochrysis species (T-ISO). Under all conditions, larvae grew at constant rates, as determined by measurements of shell length and tissue biomass. Most larvae eventually underwent spontaneous metamorphosis. Regardless of temperature, faster growth was associated with a shorter planktonic stage prior to spontaneous metamorphosis. Within an experiment, higher temperatures generally accelerated growth rates and reduced the number of days from hatching to spontaneous metamorphosis. However, growth rates were independent of temperature for larvae fed ISO at 25 and 29°C and for larvae fed T-ISO at 20 and 25°C. Where growth rates were unaffected by temperature, time to spontaneous metamorphosis was similarly unaffected. Maximum durations of larval life at a given temperature were shorter for larvae of Crepidula plana than for those of the congener C. fornicata (L.), although both species grew at comparable rates. Interpretations of the ecological significance of these interspecific differences in delay capabilities will require additional data on adult distributions and larval dispersal patterns in the field.     

Ontogenetic alterations in the gross tooth morphology of Dicamptodon and Rhyacotriton (amphibia,urodela, and dicamptodontidae)

During ontogeny, the apical and basal components of dicamptodontid teeth exhibit three major developmental stages: nonpedicellate, subpedicellate, and pedicellate. Premetamorphic larvae tend to have nonpedicellate teeth, incompletely or recently metamorphosed individuals tend to have subpedicellate teeth, and fully transformed adults usually have pedicellate teeth. In concert with this transition, cusp morphology is modified from a larval monocuspid, to an incipiently bicuspid, to definitive adult bicuspid, and finally to an adult monocuspid condition. Thus, the larval and adult monocuspid conditions are ontogenetically distinct. The morphology of the larval monocuspid, adult bicuspid, and adult monocuspid conditions differs between Dicamptodon and Rhyacotriton. However, the incipient bicuspid condition in these two genera is very similar in appearance, suggesting that Dicamptodon and Rhyacotriton may be more closely related to each other than to the family Ambystomatidae in which they both sometimes are placed. The method of establishing ontogenetic trajectories seems to be preferable to comparisons based on adult structure, since similarities in the morphology of adults often is owing to convergent or parallel evolution.     

Siphonariid development: Quintessential euthyneuran larva with a mantle fold innovation (Gastropoda; Panpulmonata)

Recent phylogenetic revisions of euthyneuran gastropods (“opisthobranchs” and “pulmonates”) suggest that clades with a planktotrophic larva, the ancestral life history for euthyneurans, are more widely distributed along the trunk of the euthyneuran tree than previously realized. There is some indication that the planktotrophic larva of euthyneurans has distinctive features, but information to date has come mainly from traditional “opisthobranch” groups. Much less is known about planktotrophic “pulmonate” larvae. If planktotrophic larvae of “pulmonates” share unique traits with those of “opisthobranchs,” then a distinctive euthyneuran larval-type has been the developmental starting template for a spectacular amount of evolved morphological and ecological disparity among adult euthyneurans. We studied development of a siphonariid by preparing sections of larval and postmetamorphic stages for histological and ultrastructural analysis, together with 3D reconstructions and data from immunolabeling of the larval apical sensory organ. We also sought a developmental explanation for the unusual arrangement of shell-attached, dorso-ventral muscles relative to the mantle cavity of adult siphonariids. Adult siphonariids (“false limpets”) have a patelliform shell but their C-shaped shell muscle partially embraces a central mantle cavity, which is different from the arrangement of these components in patellogastropods (“true limpets”). It is not obvious how shell muscles extending into the foot become placed anterior to the mantle cavity during siphonariid development from a veliger larva. We found that planktotrophic larvae of Siphonaria denticulata are extremely similar to previously described, planktotrophic “opisthobranch” larvae. To emphasize this point, we update a list of distinctive characteristics of planktotrophic euthyneuran larvae, which can anchor future studies on the impressive evolvability of this larval-type. We also describe how premetamorphic and postmetamorphic morphogenesis of larval mantle fold tissue creates the unusual arrangement of shell-muscles and mantle cavity in siphonariids. This result adds to the known postmetamorphic evolutionary innovations involving mantle fold tissue among euthyneurans.     

Neuromuscular development in Patellogastropoda (Mollusca: Gastropoda) and its importance for reconstructing ancestral gastropod bodyplan features

Within Gastropoda, limpets (Patellogastropoda) are considered the most basal branching taxon and its representatives are thus crucial for research into evolutionary questions. Here, we describe the development of the neuromuscular system in Lottia cf. kogamogai. In trochophore larvae, first serotonin‐like immunoreactivity (lir) appears in the apical organ and in the prototroch nerve ring. The arrangement and number of serotonin‐lir cells in the apical organ (three flask‐shaped, two round cells) are strikingly similar to those in putatively derived gastropods. First, FMRFamide‐lir appears in veliger larvae in the Anlagen of the future adult nervous system including the cerebral and pedal ganglia. As in other gastropods, the larvae of this limpet show one main and one accessory retractor as well as a pedal retractor and a prototroch muscle ring. Of these, only the pedal retractor persists until after metamorphosis and is part of the adult shell musculature. We found a hitherto undescribed, paired muscle that inserts at the base of the foot and runs towards the base of the tentacles. An apical organ with flask‐shaped cells, one main and one accessory retractor muscle is commonly found among gastropod larvae and thus might have been part of the last common ancestor.