Muscle development in the Japanese flounder,Paralichthys olivaceus,with special reference to some of the larval‐specific muscles

We investigated muscle development in the Japanese flounder Paralichthys olivaceus, focusing primarily on the cranial muscles, using a whole mount immunohistochemical staining method. It is well established that during the very early stages of morphogenesis, until 4 days post hatching (dph), muscles required for feeding develop. Later, between 8 and 16 dph, the muscle composition in the dorsal branchial arches changes to the adult form. We discovered the presence of larval‐specific muscles in this ontogenetic period, termed the larval branchial levators 2 and 3, located in the dorsal branchial arches. The larval branchial levators 2 and 3 disappear during the course of development, whereas the others remain as levator internus 1 and levator posterior, which have also been described in adult fish. In place of these regressed muscles, the levatores externi and levator internus 2 develop and regulate the branchial arches. In addition, we found that the levator posterior, which is thought to represent the fifth levator externus, and the levatores externi exhibit different origins. We also found that at least a part of the caudal fin musculature develops from the trunk myotome. J. Morphol. 2010. © 2010 Wiley‐Liss, Inc.     

Homologies of the branchial arch muscles in Zacco platypus (Teleostei: Cypriniformes: Cyprinidae): Evidence from innervation pattern

Homologies of the branchial arch muscles in the cyprinid Zacco platypus are assessed based on their innervation. Muscles serving the first gill arch are innervated by branches of the glossopharyngeal (IX) nerve and those serving other arches by the vagal (X) nerve. Absence of the levator posterior is confirmed. Five pairs of muscles originating from the cranium and inserted onto the specialized 5th ceratobranchial, all unique to cyprinids, are innervated by the 4th branchial trunks of X, indicating that all pairs are derivatives of the sphincter oesophagi, involving reorganization from intrinsic to extrinsic elements. Homologies of some ventral branchial muscles are also discussed and the criteria for homology improved by clarifying the innervation pattern. J. Morphol., 2011. © 2011 Wiley‐Liss, Inc.     

Development of the pharyngeal arch skeleton in Catostomus commersonii (Teleostei: Cypriniformes)

Skeletal elements of the gill arches of adult cypriniform fishes vary widely in number, size, and shape and are important characters in morphologically based phylogenetic studies. Understanding the developmental basis for this variation is thus phylogenetically significant but also important in relation to the many developmental genetic and molecularly based studies of the early developing and hence experimentally tractable gill arches in the zebrafish, a cyprinid cypriniform. We describe the sequence of the chondrification and ossification of the pharyngeal arches and associated dermal bones from Catostomus commersonii (Catostomidae, Cypriniformes) and make selected comparisons to other similarly described pharyngeal arches. We noted shared spatial trends in arch development including the formation of ventral cartilages before dorsal and anterior cartilages before posterior. Qualitatively variable gill arch elements in Cypriniformes including pharyngobranchial 1, pharyngobranchial 4, and the sublingual are the last such elements to chondrify in C. commersonii. We show that the sublingual bone in C. commersonii has two cartilaginous precursors that fuse and ossify to form the single bone in adults. This indicates homology of the sublingual in catostomids to the two sublingual bones in the adults of cobitids and balitorids. Intriguing patterns of fusion and segmentation of the cartilages in the pharyngeal arches were discovered. These include the individuation of the basihyal and anterior copula through segmentation of a single cartilage rod, fusion of cartilaginous basibranchials 4 and 5, and fusion of hypobranchial 4 with ceratobranchial 4. Such “fluidity” in cartilage patterning may be widespread in fishes and requires further comparative developmental studies. J. Morphol., 2009. © 2008 Wiley‐Liss, Inc.     

Branchial arch muscle innervation by the glossopharyngeal (IX) and vagal (X) nerves in tetraodontiformes, with special reference to muscle homologies

Branchial arch muscle innervation by the glossopharyngeal (IX) and vagal (X) nerves in 10 tetraodontiform families and five outgroup taxa was examined, with special reference to muscle homologies. Basic innervation patterns and their variations were described for all muscle elements (except gill filament muscles). In the tetraodontids Takifugu poecilonotus and Canthigaster rivulata, diodontid Diodon holocanthus, and molid Mola mola, levator externus 4 was innervated by the 3rd vagal branchial trunk (BX3) in addition to BX2, owing to strong posterior expansion of the muscle. Based on nerve innervation, migrations of the muscle attachment sites (i.e., origins and insertions) were recognized in levator internus 2 (in Mola mola), obliquus dorsalis 3 (in Ostracion immaculatus and Canthigaster rivulata), and obliquus ventralis 2 (in Stephanolepis cirrhifer), muscle topologies not necessarily being indicative of homologies. Embryonic origin of the retractor dorsalis and parallel attainment of the swimbladder muscle within the order were also discussed.     

Segmentation and fusion on the midline: Basibranchial homologies in cypriniform fishes

The development and homologies of the median elements of the ventral hyoid and branchial arches of Cypriniformes have been unclear. We compared the developmental morphology of this region across five species (Cycleptus elongatus, Luxilus zonatus, Danio rerio, Devario auropurpureus, and Cobitis striata), representing three of five major clades of cypriniforms. The development of basibranchial 1 is similar in catostomids and cyprinids, where a single, elongate, basihyal + anterior copula divides into separate elements. A gap develops between the posterior end of the basihyal cartilage and the anterior copula in catostomids but in cyprinids (Luxiluszonatus, Danio rerio, and Devarioauropurpureus) there is little separation and the basihyal and basibranchial 1 may grow close together or retain a cartilaginous connection (Danio rerio, several outgroups). In loaches and Gyrinocheilus, the gap posterior to the basihyal has been alternately interpreted as either the absence or posterior displacement of basibranchial 1. Uniquely among examined species, in Cobitis striata, the basihyal cartilage and anterior copula form as separate cartilages and remain distinct throughout development with a prominent gap between the basihyal and most anterior basibranchial, which we interpret as loss of basibranchial 1. In the posterior region associated with branchial arches 4 and 5, all examined species except Danio rerio, which has only a basibranchial 4 cartilage, have separate basibranchial 4 and 5 cartilages in early ontogeny. Basibranchials 4 and 5 remain separate in Cycleptus elongatus, Devario auropurpurea, and Cobitis striata, but fuse in Luxilus zonatus to form a posterior copula. The orientation of basibranchial 4 and 5 cartilages in Cobitis striata is similar to catostomids and cyprinids. The most posterior median element in the branchial arches, the post‐ceratobranchial cartilage, generally forms as a separate cartilage in catostomids but in Cobitis striata is connected with basibranchial 5 cartilage from earliest appearance. J. Morphol., 2012. © 2012 Wiley Periodicals, Inc.     

Comment on ‘Stable isotopes challenge the perception of ocean sunfish Mola mola as obligate jellyfish predators'

Muscle development in the bamboo sole Heteromycteris japonicus was investigated, focusing primarily on the cranial muscles, using an improved whole mount immunohistochemical staining method with potassium hydroxide, hydrogen peroxide and trypsin. Larvae of H. japonicus had branchial levators, but not all of them were retained in adults, a condition also seen in the Japanese flounder Paralichthys olivaceus. In particular, larval branchial levators II and III disappeared during development, while I and IV remained to become the levator internus I and levator posterior, which were well‐defined muscles in adults. In place of the atrophied muscles, levatores externi and levator internus II developed and regulated the branchial arches. The results showed that the muscle composition in the dorsal branchial arches changed to the adult form before metamorphosis in H. japonicus, as seen in P. olivaceus, and this transformation may be common to all members of that group.     

PHOSPHATIZED SOFT-TISSUE IN TRIASSIC BIVALVES

Abstract: Exceptionally preserved specimens of the genera Myophoria, Neoschizodus and Trigonodus (Bivalvia, Palaeoheterodonta, Trigonioida) from carbonate sediments of the Muschelkalk (Anisian, Ladinian) contain phosphatized soft‐tissues. This is the oldest record of soft‐tissue preservation in bivalves and the first from the German Muschelkalk. The phosphatized remains are here interpreted as relics of the originally chitinous gill supports, the gill axis, the labial palps (?), the adductor muscles, the pedal retractor muscles, the mantle margin including the radial mantle musculature, and the ‘siphons’. According to microprobe analysis, the mineral replacing the soft‐tissue is mainly apatite and, more rarely, francolite. Additionally, quartz filled voids within the gill supports, and in one sample it occurs in minute crystals in the phosphatized remains of the adductor muscle of Neoschizodus. Myophoria, Neoschizodus and Trigonodus were soft‐bottom dwellers and five of the specimens were discovered in life position. This is indicated by geopetal structures in three specimens.     

Evolutionary origin of the insect wing via integration of two developmental modules

SUMMARY Insect wing is a key evolutionary innovation for insect radiation, but its origins and intermediate forms are absent from the fossil record. To understand the ancestral state of the wing, expression of three key regulatory genes in insect wing development, wingless (wg), vestigial (vg), and apterous (ap) was studied in two basal insects, mayfly and bristletail. These basal insects develop dorsal limb branches, tracheal gill and stylus, respectively, that have been considered candidates for wing origin. Here we show that wg and vg are expressed in primordia for tracheal gill and stylus. Those primordia are all located in the lateral body region marked by down‐regulation of early segmental wg stripes, but differ in their dorsal–ventral position, indicating their positions drifted within the lateral body region. On the other hand, ap expression was detected in terga of mayfly and bristletail. Notably, the extensive outgrowth of the paranotal lobe of apterygote bristletail developed from the border of ap‐expressing tergal margin, and also expressed wg and vg. The data suggest that two regulatory modules involving wg–vg are present in apterygote insects: one associated with lateral body region and induces stick‐like dorsal limb branches, the other associated with the boundary of dorsal and lateral body regions and the flat outgrowth of their interface. A combinatorial model is proposed in which dorsal limb branch was incorporated into dorsal–lateral boundary and acquired flat limb morphology through integration of the two wg–vg modules, allowing rapid evolution of the wing.     

Morphology of the Parrotfish Pharyngeal Jaw Apparatus

SYNOPSIS. Analysis of the anatomy of the pharyngeal apparatusof parrotfish demonstrates extraordinary specialization of thegrinding jaws. The epibranchials have lost their gill-bearingfunction. The first epibranchial is the structural element ofthe pharyngeal valve that is operated by the first levator externus,first branchial adductor and part one of the transversus dorsalismuscles. Five pairs of muscles (fourth levator externus, levatorposterior lateralis and medialis, fifth branchial adductor,part two of the transversus ventralis) are positioned to adductthe lower pharyngeal. The retractor dorsalis and fourth obliquusdorsalis are positioned to retract the upper pharyngeal. Thethird levator internus and transversus dorsalis posterior protractthe upper pharyngeal. The fourth levator externus, both partsof the levator posterior and the fifth adductor are massiveand pinnate. Deep fossae for the attachment of the fourth levatorexternus and levator posterior muscles are sculpted out of theneurocranium. A ventral spike process of the prootic and expandedhemal postzygapophyses of the first three vertebrae are skeletalfeatures associated with the elaborated musculature of the pharynx.Synovial joints are present between the basicranium and upperpharyngeals, between the upper pharyngeals and fourth epibranchialsand between the lower pharyngeal and cleithrum. The upper pharyngealsact as a single unit bound by cruciate ligaments. The fourthepibranchial is a key element in the pharyngeal apparatus andserves to direct forces generated by the transversus ventralis,fifth adductor, levator posterior lateralis, transversus dorsalisposterior and fourth obliquus dorsalis.     

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.     

Ontogeny of the jaw and maxillary barbel musculature in the armoured catfish families Loricariidae and Callichthyidae (Loricarioidea,Siluriformes), with a discussion on muscle homologies

The neotropical loricarioid catfishes include six families, the most species‐rich of which are the Callichthyidae and the Loricariidae. Loricariidae (suckermouth armoured catfishes) have a highly specialized head morphology, including an exceptionally large number of muscles derived from the adductor mandibulae complex and the adductor arcus palatini. Terminology of these muscles varies among the literature, and no data exist on their ontogenetic origin. A detailed examination of the ontogeny of both a callichthyid and a loricariid representative now reveals the identity of the jaw and maxillary barbel musculature, and supports new hypotheses concerning homologies. The adductor mandibulae muscle itself is homologous to the A1‐OST and A3′ of basal catfishes, and the A3′ has given rise to the newly evolved loricariid retractor veli as well. The A2 and A3″ have resulted in the retractor tentaculi of Callichthyidae and the retractor premaxillae of Loricariidae. Thus, these two muscles are shown to be homologous. In Loricariidae, the extensor tentaculi consists of two separate muscles inserting on the autopalatine, and evidence is given on the evolutionary origin of the loricariid levator tentaculi (previously and erroneously known as retractor tentaculi) from the extensor tentaculi, and not the adductor mandibulae complex. © 2009 The Linnean Society of London, Zoological Journal of the Linnean Society, 2009, 155 , 76–96.     

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.     

Beziehungen zwischen Körperbau und Lebensweise bei Blenniidae (Pisces) des Roten Meeres

The muscle and skeleton anatomy of the pectoral, pelvic, and anal fins are described in 3 Salariin Blenniidae: Salarias fasciatus (sublittoral), Istiblennius edentulus (eulittoral), Alticus kirkii (supralittoral). In A. kirkii these organs are adapted to a climbing habit on the steep rocks beyond the water. The results are compared with those found in Periophthalmus.

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Abbildungserklärungen B Basale - Cl Cleithrum - Co Coracoid - Creld Crista cleithri dorsalis - Crele Crista cleithri externa - H Haken an den Lepidotrichen der Ventralia - Lep Lepidotrichen - Pel Postcleithrum - Prsv Processus spinae ventralis - Pt Posttemporale - Rad Radiale - Scl Supracleithrum - SCl Symphyse des Cleithrum - Scp Scapula - abpr M. abductor profundus - adpr M. adductor profundus - arre M. arrector externus - arri M. arrector internus - cord M. coraco-radialis - dep M. depressor (Analis) - dprrd M. depressor radiorum (Pectoralia) - er M. erector - extpr M. extensor proprius - fls M. flexor superficialis - inc M. inclinator - levs M. levator superficialis - mes M. mesoventralis - rtrd M. retractor dorsalis - rtris M. retractor ischii - rtrv M. retractor ventralis Mit Unterstützung der Deutschen Forschungsgemeinschaft.     

Comparative myology of the mandibular and hyoid arches of sharks of the order hexanchiformes and their bearing on its monophyly and phylogenetic relationships (Chondrichthyes: Elasmobranchii)

The order Hexanchiformes currently comprises two families, Chlamydoselachidae (frilled sharks) and Hexanchidae (six‐ and seven‐gill sharks), but its monophyly and relationships with other elasmobranchs are still discussed. Previous studies of hexanchiforms addressing these issues were based mainly on external morphology, teeth, skeletal features, and molecular data, whereas the employment of characters derived from variations in muscles has not been significantly explored. Dissections of four species of Hexanchiformes (including Chlamydoselachus anguineus) are reported here describing the mandibular (musculus adductor mandibulae dorsalis, m. adductor mandibulae ventralis, m. levator labii superioris, m. intermandibularis, and m. constrictor dorsalis) and hyoidean (m. constrictor hyoideus dorsalis and ventralis) arch muscles. Our results provide new data concerning the relationships of hexanchiforms to other elasmobranchs. The m. adductor mandibulae superficialis is described and illustrated in C. anguineus, contradicting previous accounts in which is was considered absent. The anteroposterior orientation of the m. adductor mandibulae superficialis in Chlamydoselachus is similar to the pattern found in hexanchids, squaloids, and hypnosqualeans (including batoids), suggesting it was secondarily lost in Echinorhinus. This muscle therefore provides further support for the inclusion of the Chlamydoselachidae and Hexanchidae in the Squalomorphi, and not basal to all other elasmobranchs or nested within an all‐shark collective, as has been previously proposed. However, the m. adductor mandibulae superficialis originating at the jaw joint and with an aponeurotic insertion in hexanchids, squaliforms, and hypnosqualeans, may be a separate derived feature uniting these taxa. The insertion of the m. constrictor dorsalis is restricted to the postorbital articulation in hexanchids, whereas it extends farther anteriorly in C. anguineus. The insertion of the m. constrictor hyoideus dorsalis solely on the palatoquadrate is found exclusively in the Hexanchidae. We conclude that no specific pattern of mandibular or hyoid arch muscles support the monophyly of hexanchiforms (i.e., including Chlamydoselachus). J. Morphol., 2013. © 2012 Wiley Periodicals, Inc.     

Abrupt changes in defence and trophic morphology of the giant threespine stickleback (Gasterosteus sp.) following colonization of a vacant habitat

To evaluate the first stages of adaptation and differentiation following colonization into a vacant and ecologically divergent habitat, 100 melanistic and low‐plated adult threespine stickleback (Gasterosteus aculeatus) exhibiting gigantism in body size and robust spines were transferred in 1993 from a large dystrophic lake (Mayer Lake, Haida Gwaii, British Columbia, Canada) with a diverse vertebrate predator regime, into an adjacent fishless eutrophic pond with macroinvertebrate piscivores. Eight generations were examined as a test of multiple functional hypotheses on the morphological traits that differentiate lake and pond stickleback throughout their distribution. Measurements of 20 defence and trophic traits were made on 275 wild‐caught fish collected from the source and transplant populations over multiple years. There have been significant reductions (males: females) in plate count (8%: 0.5%), lateral plate 2 frequency (46%: 17%), lateral plate 3 height (17%: 18%), pelvic spine length (12%: 6%), dorsal spine length (21%: 16%), gill raker number (5%: 1%), and gill raker length (37%: 43%), and an increase in gill raker spacing (+5%: 0%), jaw length (+5%: +4%), and eye diameter (+8%: +7%). These changes within eight generations represent one‐third of the morphological differences observed between naturally established large lake and pond populations in these archipelago and are all in the direction predicted from the change in habitat. Field samples indicate strong selection in the colonists although lab‐reared individuals implicate an additional role of plasticity for dorsal spine and gill raker lengths, which may contribute to the rapid adaptation into novel and highly divergent selective landscapes. © 2012 The Linnean Society of London, Biological Journal of the Linnean Society, 2012, 107 , 494–509.     

Gill‐derived glands in species of Astyanax (Teleostei: Characidae)

The presence of a gill‐derived gland is herein reported for the first time in males of species of Astyanax and related genera; they are described through histological cuts and SEM. The gill‐derived glands described for the Characidae, when fully developed, present a similar structure in different species. The main external feature of gill‐derived glands is the fusion of anteriormost gill filaments on the ventral branch of first gill arch. This fusion is caused by squamous stratified epithelial tissue that covers adjacent filaments, forming a series of chambers. In the region where the gill‐derived gland develops, the secondary lamellae of the gill filaments are much reduced or completely atrophied being characterized by the presence of glandular cells forming nests.     

Description of a new species of Triplophysa (Teleostei: Nemacheilidae) from Guizhou Province,China

A new cave‐dwelling fish species Triplophysa guizhouensis is described based on specimens collected from Guizhou, China, in a subterranean system interconnected with the Hongshui River drainage. The species can be distinguished from its congeners by a combination of characters: eyes present; caudal fin with 14 branched rays; inner gill rakers of first gill arch 8–10; posterior chamber of air bladder developed; and body posterior of dorsal fin scaled. A key to species of Triplophysa in the Pearl River basin is provided.     

Innervation pattern of the gill arches and gills of the carp (Cyprinus carpio)

The innervation pattern of the respiratory gill arches of the carp (Cyprinus carpio) is described. The gill region is innervated by the branchial branches of the glossopharyngeal and vagal nerves. Each branchial nerve divides at the level of or just distal to the epibranchial ganglion into: 1) a pretrematic branch, 2) a dorsal pharyngeal branch, and 3) a posttrematic branch. The dorsal pharyngeal branch innervates the palatal organ in the roof of the buccal cavity. The pretrematic and posttrematic branches innervate the posterior and anterior halves, respectively, of the gill arches bordering a gill slit. Each branch splits into an internal and an external part. The internal bundle innervates the buccal side of the gill arch, including the gill rakers. The external bundle terminates in the gill filaments. The epibranchial motor branch, a small nerve bundle containing only motor fibers, circumvents the ganglion and anastomoses distally with the posttrematic branch. The detailed course and branching patterns of these branches are described.     

Myogenesis in two polyclad platyhelminths with indirect development,Pseudoceros canadensis and Stylostomum sanjuania

SUMMARY Myogenesis of two representatives of Platyhelminthes, Stylostomum sanjuania and Pseudoceros canadensis, was followed from egg deposition until well‐differentiated free‐swimming larval stages, using F‐actin staining and confocal laserscanning microscopy. Zonulae adhaerentes are the only structures to stain before 50% of development between egg deposition and hatching in S. sanjuania, and before 67% of development in P. canadenis. Subsequently, irregular fibers appear in the embryo, followed by a helicoid muscle close to the apical pole. Three longitudinal muscle pairs form, of which the dorsal pair remains more pronounced than the others. Gradually, new muscles form by branching or from double‐stranded muscle zones adjacent to existing muscles. This results in an elaborate muscular bodywall that consists of a single helicoid muscle as well as multiple circular and longitudinal muscles. Diverse retractor muscles insert at the sphincter muscles around the stomodeum. The overall arrangement and formation mode of the larval musculature appears very similar in both species, although only P. canadensis has a primary circular muscle posterior to the helicoid muscle. Muscle formation in the apical region of the embryo precedes that at the abapical pole and the primary longitudinal muscles form slightly later than the primary circular muscles. Myogenesis and larval myoanatomy appears highly conserved among polyclad flatworms, but differs significantly from that of other trochozoan clades. Our data suggest that the larval muscular ground pattern of polyclad larvae comprises a bodywall consisting of a helicoid muscle, circular and longitudinal muscles, several retractor muscles, and sphincter muscles around the stomodeum.     

Danionella dracula,an escape from the cypriniform Bauplan via developmental truncation?

We provide a detailed account of the osteology of the miniature Asian freshwater cyprinid fish Danionella dracula. The skeleton of D. dracula shows a high degree of developmental truncation when compared to most other cyprinids, including its close relative the zebrafish Danio rerio. Sixty‐one bones, parts thereof or cartilages present in most other cyprinids are missing in D. dracula. This impressive organism‐wide case of progenesis renders it one of the most developmentally truncated bony fishes or even vertebrates. Danionella dracula lacks six of the eight unique synapomorphies that define the order Cypriniformes and has, thus, departed from the cypriniform Bauplan more dramatically than any other member of this group. This escape from one of the most successful Baupläne among bony fishes may have been facilitated by the organism‐wide progenesis encountered in D. dracula. By returning in its skeletal structure to the early developmental condition of other cypriniforms, D. dracula may have managed to overcome the evolutionary constraints associated with this Bauplan and opened up new evolutionary avenues that enabled it to evolve a number of striking morphological novelties, including its tooth‐like odontoid processes and a complex drumming apparatus. J. Morphol. 277:147–166, 2016. © 2015 Wiley Periodicals, Inc.