Inferring muscular ground patterns in Bivalvia: Myogenesis in the scallop Nodipecten nodosus
© Audino et al. 2015
Received: 4 September 2015
Accepted: 5 November 2015
Published: 2 December 2015
Myogenesis is currently investigated in a number of invertebrate taxa using combined techniques, including fluorescence labeling, confocal microscopy, and 3D imaging, in order to understand anatomical and functional issues and to contribute to evolutionary questions. Although developmental studies on the gross morphology of bivalves have been extensively pursued, organogenesis including muscle development has been scarcely investigated so far.
The present study describes in detail myogenesis in the scallop Nodipecten nodosus (Linnaeus, 1758) during larval and postmetamorphic stages by means of light, electron, and confocal microscopy. The veliger muscle system consists of an anterior adductor muscle, as well as four branched pairs of striated velum retractors and two pairs of striated ventral larval retractors. The pediveliger stage exhibits a considerably elaborated musculature comprising the velum retractors, the future adult foot retractor, mantle (pallial) muscles, and the anterior and posterior adductors, both composed of smooth and striated portions. During metamorphosis, all larval retractors together with the anterior adductor degenerate, resulting in the adult monomyarian condition, whereby the posterior adductor retains both myofiber types. Three muscle groups, i.e., the posterior adductor, foot retractor, and pallial muscles, have their origin prior to metamorphosis and are subsequently remodeled.
Our data suggest a dimyarian condition (i.e., the presence of an anterior and a posterior adductor in the adult) as the basal condition for pectinids. Comparative analysis of myogenesis across Bivalvia strongly argues for ontogenetic and evolutionary independence of larval retractors from the adult musculature, as well as a complex set of larval retractor muscles in the last common bivalve ancestor.
KeywordsBivalve EvoDevo Evolution Morphology Musculature Morphogenesis Ontogeny Pectinid
Ontogeny of bivalve gross anatomy has been widely investigated during the past two centuries and bivalve larvae have been used as models in studies dealing with diverse biological questions (e.g., [1, 2]). Developmental studies in this class-level taxon of mollusks have been performed for numerous species using light and electron microscopy, and a large bulk of data on larval general morphology is available (e.g., [3, 4]). Nevertheless, several gaps of knowledge on bivalve development remain, especially on myogenesis, neurogenesis, and morphogenesis of other organ systems [5–7].
Morphological investigations have significantly contributed to understanding the function of animal organ systems and the evolution of phenotypic diversity. In particular, the relevance of morphology for EvoDevo approaches has been highlighted as being indispensable for reconstruction of phenotypic ground patterns and character evolution (see ). Modern methods including fluorescence staining combined with confocal microscopy and three-dimensional reconstruction have been successfully applied in the last decade to study invertebrate organogenesis, including muscular development (see [9, 10] for reviews). Such techniques, particularly phalloidin staining, represent a powerful tool for studies into the microanatomy and development of the often complex musculature, in particular of minute organisms including invertebrate larvae.
Within Mollusca, a solid database exists for a number of class-level taxa including the Gastropoda (e.g., [11–13]), Scaphopoda , Polyplacophora , and Neomeniomorpha (= Solenogastres) [16, 17]. The data generated have yielded important insights into developmental and evolutionary pathways within the phylum such as, for example, the emergence of the neomeniomorph worm-like body from a much more complex ancestor (see  for extensive review on the current state-of-the-art of molluscan EvoDevo). Despite this recent progress, data on myogenesis are particularly scarce for the second-largest molluscan class, the Bivalvia. Thereby, the most complete data are currently available for two species only, namely the mytilid Mytilus trossulus [18, 19] and the teredinid shipworm Lyrodus pedicellatus .
Pectinidae (scallops) comprises a very diverse family of pteriomorphian epifaunal bivalves, but despite a broad knowledge on larval anatomy and preliminary characterization of larval muscles in Pecten maximus , no further details on scallop muscle development are available. To inject novel data into the discussion of shared and diverging morphological characters within Pectinidae and across Bivalvia, and to reconstruct potential bivalve larval ground patterns, the present study provides a detailed description of myogenesis in the scallop Nodipecten nodosus (Linnaeus, 1758) during larval and postmetamorphic development.
Herein, designation of larval orientation and body axes are used in accordance with comparative lophotrochozoan larval anatomy (e.g., ). In larvae, anterior corresponds to the position of the apical tuft, posterior to the opposite region, and ventral is defined by the position of the foot (see also ), i.e., for veliger larvae we consider herein the velum region as anterior and the hinge as posterior. We follow this nomenclature for all larval muscles but not for the future adult “anterior adductor” (larval dorsal) and “posterior adductor” (larval ventral), respectively, to avoid confusion when comparing larval and adult conditions. In postmetamorphic bivalves, body rotation may result in deep changes in morphology and, consequently, in nomenclatorial conflicts. Consensually, adult axes designation in bivalves is commonly such that the mouth position defines anterior and the shell hinge dorsal (with the opposite as ventral).
Two additional, distinct pairs of muscles, termed herein ventral larval retractors, also formed by striated fibers, are found attached in a more ventral region of the larva (Fig. 1d). The posterior ventral larval retractors branch before reaching the ventral body wall, while the anterior ventral larval retractor has an additional branch running towards the median portion of the larval body (Fig. 1d). The anterior adductor muscle is already present at this stage and comprises two portions: a slightly thinner one, composed of smooth fibers, that is situated more anteriorly, and a larger one composed of striated fibers that is more posteriorly located (Fig. 1e).
The mantle margin of the pediveliger exhibits muscles running along its extension (Fig. 2d), a condition not present in earlier stages. Such muscles are comprised of margin-parallel fibers (apparently including striated and smooth fibers) and retractor bundles (striated fibers only), indicating the onset of development of the mantle retractors (Fig. 2d).
General notes on the development of pectinid bivalves
Embryonic and larval development in pectinids has been studied for commercial purposes, yielding a bulk of data on shell development and gross morphology (e.g., [23–27]). However, details on organogenesis, including neuromuscular development, are rare and are only available for Pecten maximus and Argopecten purpuratus, which have been studied using light and electron microscopy techniques [21, 28]. Myogenesis in Nodipecten nodosus, as described herein, represents a significant input of anatomical features and the dynamics of their ontogenetic establishment and remodeling during scallop development and thus contributes significantly to a broader understanding of myogenesis and larval myoanatomy in bivalves.
Velum retractor muscles
Dorsal velum retractor
Velum retractor 1
Dorsal velum retractor
Medio-dorsal velum retractor
Velum retractor 2
Ventral velum retractor
Medio-ventral velum retractor
Velum retractor 3
Ventral velum retractor
Velum retractor 4
Ventral larval retractors
Posterior ventral larval retractor
Posterior retractor 1
Ventral larval retractor
Anterior ventral larval retractor
Posterior retractor 2
Posterior retractor 3
While four pairs of velum retractors were observed in Nodipecten nodosus, Pecten maximus , Argopecten purpuratus , and Crassostrea gigas , three pairs are present in Mytiuls trossulus  and Lasaea adansonii , and only two pairs in Lyrodus pedicellatus (not counting the unpaired accessory velum retractor of this species; ). Comparisons to velum retractors of M. trossulus and L. adansonii are difficult because muscle position and insertion sites are not clear. According to the thorough description of the velum retractors in L. pedicellatus larvae, the dorsal and ventral velum retractor of this species may correspond to the dorsal and medio-dorsal velum retractors of N. nodosus, respectively (Table 1). In both species, the dorsal velum retractors are dorsally attached, pass very close to the anterior adductor, and eventually reach the dorso-median region of the velum. The ventral velum retractors of L. pedicellatus and the medio-dorsal velum retractors of N. nodosus are attached to the shell slightly ventral to the dorsal velum retractor. These muscles branch and reach the velum in its most ventral portion.
Ventral larval retractors
Two pairs of shell-anchored ventral larval retractors are present in Nodipecten nodosus and in veligers of Pecten maximus (“posterior retractors”, ). Notwithstanding, a third pair of larval retractors, occupying a more anterior region, has been described for P. maximus . Similarly, three pairs of ventral larval retractors are present in the mussel Mytilus trossulus (there termed “larval protractors”; ). In contrast, a single pair of ventral larval retractors was described for the heterodonts Lyrodus pedicallatus  and Dreissena polmorpha , possibly corresponding to the posterior ventral larval retractor of N. nodosus (Table 1). In all bivalve species studied so far, this particular muscle group degenerates before metamorphosis, thus representing an ephemeral (transitory) muscle group in bivalve myogenesis [19–21].
As in Nodipecten nodosus, the development of the anterior adductor and velum retractors also occurs in early veliger stages of Argopecten purpuratus, Argopecten irradians, and Pecten maximus [2, 28, 33]. Apparently, the development of the anterior adductor prior to the posterior adductor is a common feature among bivalves (e.g., [19, 20, 30]). The dimyarian condition in early N. nodosus development confirms the ancestral condition of two adductors for pectinids and possibly the entire Bivalvia. The anterior adductor of N. nodosus comprises two portions, one composed of smooth fibers and the other of striated fibers; a similar morphology was found in A. purpuratus and P. maximus [21, 28].
Previously, it had been suggested that the foot of pectinid pediveliger larvae might originate from ventral larval retractors (“posterior retractors”, ). However, such a condition was not found during Nodipecten nodosus myogenesis, where both muscle groups are present at the pediveliger stage (Fig. 2a, d). Larvae of Lyrodus pedicellatus exhibit the developing foot retractor in a ventral position, close to the posterior adductor anlage, possibly originating at the ventral branches of some velum retractors . Our results indicate that the foot retractor in N. nodosus is formed by combined muscles originating from two distinct positions. One bundle is ventrally attached to the shell at the posterior adductor region, close to the hinge line where some velum retractors are attached. These bundles might correspond to the foot retractor anlagen observed in L. pedicellatus and Lasaea adansonii, where the foot retractor also originates in a similar position . The second group forming the foot retractor in N. nodosus seems to emerge from an anterio-ventral position, close to the median portion of the body. Our results strongly contradict the previous assumption that the (adult) scallop foot retractor derives from larval retractors , also because the muscle bundles forming the foot retractor in pediveligers of N. nodosus are composed of smooth fibers, while the larval retractors are striated. In addition, all striated larval retractors are lost during metamorphosis and are thus not incorporated into the adult bodyplan, resulting in entirely independent and de novo formation of the adult foot musculature.
Muscles associated with the pallial margin have until now received little attention in studies on bivalve development. At the pediveliger stage, smooth fibers are supposed to be found near the mantle folds in Pecten maximus , and longitudinal smooth muscles are present at the mantle rim of Lasaea adansonii, together with several mantle retractors . The larval mantle musculature in Lyrodus pedicellatus includes U-shaped muscles, which might correspond to the margin-parallel muscles observed in Nodipecten nodosus, as well as finger-shaped muscles, with no obvious correspondence to other bivalve muscles identified so far . The branched retractors and margin-parallel bundles that spread along the mantle margin of N. nodosus pediveligers are retained after metamorphosis and they suggest potential retraction of the entire margin and slight alteration of its form by muscular contractions .
Postmetamorphic muscle development
Bivalve metamorphosis has been extensively studied in several species on gross morphological level, some of them including descriptions of organ systems in the larva (e.g., [32, 35–42]). Changes in muscle system organization during metamorphosis are well known only for some species, i.e., Mytilus edulis , Mytilus trossulus , and Ostrea edulis . In Nodipecten nodosus, metamorphosis initiates a dramatic simplification of the musculature: the major portion of striated larval muscles, including all velum retractors and ventral larval retractors, is resorbed. In addition, the anterior adductor starts to degenerate and only the mantle and the posterior adductor exhibit striated muscles in postlarval stages. The postmetamorphic foot musculature is organized into a foot retractor and a pedal plexus, both composed exclusively of smooth fibers. The muscle bundle in the ventral region, close to the median portion of the velum retractors, is lost; the adult foot retractor is formed by bundles that have originated in the posterior ventral region during the pediveliger stage.
The presence of both striated and smooth muscles in the posterior adductor, as observed in Nodipecten nodosus, is a typical feature of the scallop musculature [44, 45]. The striated subset increases relative to the smooth one during postmetamorphic development. Oysters also have a posterior adductor formed by two portions; however, in these bivalves the fibers are obliquely striated, in contrast to the cross-striated pattern found in scallops [46, 47]. Interestingly, after metamorphosis, striated muscles appear to be absent in bivalves outside the Pectinidae .
Reconstructing ancestral muscular bodyplan features in Bivalvia
Details on bivalve myogenesis are only slowly emerging, but the data currently available already allow for comparisons and initial attempts to cast some light on the ground patterns of bivalve muscle morphogenesis and the evolution of larval muscular features. Recent phylogenetic hypotheses provide a suitable framework to interpret these issues within an evolutionary context (e.g., ).
A muscle ring underneath the developing velum is present in Lyrodus pedicellatus and Mytilus trossulus (but apparently absent in Nodipecten nodosus) as well as in most other molluscan larvae (see ), suggesting that it was also part of the bivalve larval ground pattern (see below and [10, 19, 20]). The larval retractor system is the most conspicuous muscular system in the bivalve larva and it addresses two main issues concerning the ancestral reconstruction of larval musculature: (i) The distribution and developmental dynamics of striated and non-striated fibers during myogenesis. While pteriomorphian bivalves such as N. nodosus, M. trossulus, and Crassostrea gigas have striated velum retractors ([6, 19]; present study), heterodont species, for example, Lasaea adansonii and L. pedicellatus, apparently only exhibit smooth velum retractors [20, 31]. (ii) The number of velum retractor pairs that varies between bivalve species  and the number of ventral larval retractors that may range from one to three (see ), including two observed in N. nodosus. This varying number of larval retractors in the few species investigated, together with the lack of information on the majority of bivalve subclades (including the putatively basal protobranchs), renders any assessment concerning the ancestral number and type of larval retractors highly speculative. In any case, our results and previous data strongly suggest that larval retractors profusely branch during larval development and undergo complete degeneration during metamorphosis, demonstrating the ontogenetic, and most likely also evolutionary, independence of the larval retractor systems from the adult bivalve musculature.
The development of the bivalve adductor systems reveals surprising differences in myofiber constitution during larval and adult stages, also in number of adductors and the dynamics of their formation and degeneration. A dimyarian condition is prevalent in bivalve myogenesis, at least in all species studied so far , even in indirect developers that exhibit a so-called pericalymma larva instead of a trochophore such as the protobranchs Nucula delphinodonta and Yoldia limatula [49, 50]. Thereby, the anterior adductor is always formed prior to the posterior one, and both adductors consist of two distinct subunits (see [20, 51]). Degeneration of the anterior adductor during metamorphosis appears typical for many pteriomorphian bivalves, confirming the notion that these bivalves also stem from an ancestor that had two adductor systems as adult. Overall, however, the assessment of homology hypotheses for adductor systems across the Bivalvia still represents a complicated issue, since different types of myofibers are present in different taxa and the adductors may be formed de novo during development, as observed in the freshwater mussel Anodonta cellensis, where the (single) adductor of the glochidium larva degenerates and the adult adductor system appears to develop independently .
A comparison of myogenesis across Mollusca reveals important insights into shared and diverging features of the larval muscular bodyplan of the various class-level taxa. As such, a prototroch muscle ring is present in bivalves [19, 31], gastropods [11, 13], polyplacophorans , and aplacophorans [16, 53], and thus appears to be a feature of the larval muscular architecture of the last common molluscan ancestor . By contrast, explicit larval retractors with distinct shell insertion sites have so far only been found in bivalves and gastropods but are absent in scaphopods, polyplacophorans, and, obviously, the shell-less aplacophorans [14, 16, 54], and thus might have evolved either independently in the respective conchiferan clades or at the base of Conchifera with secondary loss in the scaphopods.
The recent findings of a highly complex, polyplacophoran-like myoanatomy in larvae of a neomeniomorph aplacophoran [16, 17] and the description of a fossil aplacophoran with seven shell plates  argue for a complex last common aculiferan ancestor, most likely with seven-fold seriality in its dorsoventral musculature and, possibly, seven shell plates. Given the recently suggested basal dichotomy in deep molluscan phylogeny [56, 57] that proposes a split of the phylum into Aculifera (Polyplacophora, Neomeniomorpha, Chaetodermomorpha) and Conchifera (all remaining taxa), it remains unclear whether the ur-aculiferan condition of a complex body musculature was also present in the ur-mollusk. In any case, however, the comparative data presently available dramatically highlight the strong dynamics that act during the ontogenetic establishment of the musculature in the various molluscan representatives and reflect the evolutionary plasticity in the myogenetic and myoanatomical pathways at all phyletic levels within this most diverse lophotrochozoan phylum.
Specimens of Nodipecten nodosus at different developmental stages, i.e., veliger, pediveliger, postmetamorphic, and juvenile, were obtained from the scallop farm Institute of Eco-Development from Baía de Ilha Grande (IED-BIG), Rio de Janeiro, Brazil. Samples were removed from artificial hatcheries and anesthetized with 7.5 % MgCl2 prior to fixation.
Light (LM) and Transmission Electron Microscopy (TEM)
Specimens were fixed for 3 h at 4 °C in a modified Karnovsky solution (2 % paraformaldehyde + 2,5 % glutaraldehyde in 0.1 M sodium cacodylate buffer at pH 7.4 and 1osm adjusted with sucrose; ). For TEM, pediveliger larvae were postfixed for 1 h in 1 % OsO4 in buffer solution at 4 °C. For LM and TEM, larvae and juveniles were decalcified for 12 h at room temperature in 3 % ascorbic acid. Following dehydration in a graded ethanol series, specimens were embedded in Epoxy resin for TEM and glycol-methacrylate resin (Leica Historesin Kit, Germany) for LM. Serial 2–3 μm sections were obtained on a Leica RM2255 microtome (Leica, Wetzlar, Germany) for LM, and they were stained with hematoxylin and eosin or toluidine blue and basic fuchsin. Digital images were captured using a Nikon DS-Ri1 camera on a Nikon eclipse 80i microscope (Nikon Instech Co. Ltd, Kawasaki, Japan). For TEM, ultrathin sections were generated using a Leica Ultracut UCT microtome (Leica, Illinois, USA), mounted on copper slot-grids, contrasted with uranyl acetate and lead citrate, and analyzed using a Zeiss EM 900 electron microscope (Carl Zeiss, Oberkochen, Germany).
Immunocytochemistry, Confocal Laser Scanning Microscopy (CLSM), and 3D Reconstruction
Specimens were fixed in 4 % paraformaldehyde in 0.1 M phosphate buffer (PB) for 1 h, followed by four rinses in the buffer solution. Samples were stored in 0.1 M PB containing 0.1 % NaN3 at 4 °C. Decalcification of larval and postmetamorphic individuals was performed in 0.05 M EGTA for 1 h at room temperature, with a maximum of 10 individuals per 5 ml in an embryo dish. For F-actin staining, specimens were permeabilized with PBS containing 2 % Triton-X 100 (PBT) overnight and then incubated in a 1:40 dilution of Alexa Fluor 488 phalloidin (Molecular Probes) in PBT for 24 h at room temperature in the dark. Cell nuclei were stained with DAPI (4′, 6-diamidino-2-phenylindole) (Invitrogen). Then, specimens were rinsed three times in PB for about 20 min each and mounted in Fluoromount G (Southern-Biotech, Birmingham, Alabama, USA) on standard microscope slides. Analysis and image acquisition were performed on a Leica TCS SP5 II confocal laser scanning microscope equipped with the software Leica Application Suite Advanced Fluorescence (LAS AF), Version 2.6.0 (Leica Microsystems, Wetzlar, Germany). Confocal image stacks were recorded with 0.3 μm step size along the z-axis and digitally merged as maximum intensity projections. 3D reconstructions were created from selected confocal stacks using the imaging software Imaris, Version 4.1 (Bitplane, Zürich, Switzerland).
Confocal laser scanning microscopy
Hematoxylin and eosin
Phosphate buffer solution
Phosphate buffer solution containing Triton-X 100
Toluidine blue and basic fuchsin
Transmission electron microscopy
The authors acknowledge funding provided by FAPESP (2012/11708-1, 2013/17685-6; São Paulo Research Foundation) and the Lise-Meitner-Programme of the Austrian Science Fund (FWF; M1523-B19 to AK), support provided by the “Programa de Pós-Graduação em Zoologia – IB-USP”, and biological specimens provided by the Institute of Eco-Development from Baia de Ilha Grande (IED-BIG). Research in the lab of AW is further supported by a grant of the Austrian Science Fund on early molluscan development and evolution (P24276-B22). The authors acknowledge Dr. Martin Fritsch (Vienna) for invaluable assistance with the 3D reconstructions. They also thank the following laboratories and institutions that provided complementary facilities for implementation of this study: Centro de Biologia Marinha (CEBIMar-USP), Laboratório de Cultivo e Estudo de Cnidários (IB-USP), and Laboratório de Biologia Celular (IB-USP).
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