Gerhard Haszprunar

The development of the serotonergic and FMRF-amidergic nervous system in Antalis entalis (Mollusca, Scaphopoda)

The morphogenesis of serotonin- and FMRF-amide-bearing neuronal elements in the scaphopod Antalis entalis was investigated by means of antibody staining and confocal laser scanning microscopy. Nervous system development starts with the establishment of two initial, flask-like, serotonergic central cells of the larval apical organ. Slightly later, the apical organ contains four serotonergic central cells which are interconnected with two lateral serotonergic cells via lateral nerve projections. At the same time the anlage of the adult FMRF-amide-positive cerebral nervous system starts at the base of the apical organ. Subsequently, the entire neuronal complex migrates behind the prototroch and the six larval serotonergic cells lose transmitter expression prior to metamorphic competence. There are no strictly larval FMRF-amide-positive neuronal structures. The development of major adult FMRF-amide-containing components such as the cerebral system, the visceral loop, and the buccal nerve cords, however, starts before the onset of metamorphosis. The anlage of the putative cerebral system is the only site of adult serotonin expression in Antalis larvae. Establishment of the adult FMRF-amidergic and serotonergic neuronal bauplan proceeds rapidly after metamorphosis. Neurogenesis reflects the general observation that the larval phase and the expression of distinct larval morphological features are less pronounced in Scaphopoda than in Gastropoda or Bivalvia. The degeneration of the entire larval apical organ before metamorphic competence argues against an involvement of this sensory system in scaphopod metamorphosis. The lack of data on the neurogenesis in the aplacophoran taxa prevent a final conclusion regarding the plesiomorphic condition in the Mollusca. Nevertheless, the results presented herein shed doubts on general theories regarding possible functions of larval apical organs of Lophotrochozoa or even Metazoa.

Anatomy and affinities of pseudococculinid limpets (Mollusca, Archaeogastropoda)

The anatomy of 12 pseudococculinid species, representing the two subfamilies and 10 (of 11 known) genera, is described in detail. Three new genera are erected, Yaquinabyssia, Copulabyssia and Amphiplica. Subfamilial and generic systematics are reconsidered and additionally based on anatomical characters. Characters defining subfamilies and genera (Pseudoeoeculininae: Pseudococculina, Notocrater, Tentaoculus, Mcsopelex, Bandabyssia, Kurilabyssia; Caymanabyssiinae: Caymanabyssia, Colotrachelus, Yuquinabyssia, Copulabyssia, Amphiplica) are the modifications in shell and radula, the number and arrangement of gill‐leaflets, the size of the pedal gland, the degree of eye‐reduction and the modifications of the seminal groove and of the copulatory organ. Separation of the Pseudococculinidae Hiekman, 1983 from the Cocculinidae Dall, 1882 at the superfamilial level is confirmed by great differences in their anatomy. Whereas the Cocculinidae are closely related to the Bathysciadiidae (Cocculinoidea). the Lepctcllidae, Pyropeltidae, Pseudococculinidae,? Bathyphytophilidae, Osteopeltidae, Cocculinellidae, Addisoniidae and Choristellidae form a clearly separated supcrfamily (Lepetelloidea). Both superfamilies compose the Cocculiniformia. a primitive but highly specialized arehaeogastropod suborder.

Zur Anatomie und systematischen Stellung der Architectonicidae (Mollusca, Allogastropoda)

The anatomy of the Architectonicidae is described. The family combines prosobranch and pentaganglionate (=euthyneuran) traits, but has evolved in a very specialized way as cnidaria‐feeders. There is no close relationship to the Epitoniidae, and the taxon ‘Heterogastropoda’ is regarded as artificial. The closest relatives of the Architectonicidae are the Mathildidae and the Pyramidellidae, all united in a taxon Allogastropoda. This taxon is regarded as a connecting link between basal marine Caenogastropoda and the most primitive Pentaganglionata (e.g. Acteon, Ringicula). The relationships of the Architectonicidae to the Rissoellidae and Omalogyridae are briefly discussed.

On the Anatomy and Systematic Position of the Mathildidae (Mollusca, Allogastropoda)

The anatomy of two mathildid species, Opimilda maoria Powell, 1940 and Gegania valkyrie Powell, 1971 has been investigated using serial sections. The mathildid anatomy strongly resembles that of the Architectonicidae, and therefore both families are included in the superfamily Architectonicoidea. The buccal system of Gegania valkyrie is the most primitive of all Allogastropoda (Architectonicoidea and Pyramidelloidea) so far investigated. Reproductive features within with Architectonicoidea vary. Certain species (Gegania valkyrie) are hermaphrodites, whilst others (Opimilda maoria) appear to be gonochorists; in these species males also possess a (sperm‐filled) receptaculum seminis. Similar genital and reproductive features are found in the prosobranch relict species Campanile symbolicum Iredale, 1917, the systematic position of which is discussed briefly.

Anatomy and systematics of bathyphytophilid limpets (Mollusca, Archaeogastropoda) from the northeastern Pacific

Bathyphytophilus diegensis sp. n. is described on basis of shell and radula characters. The radula of another species of Bathyphytophilus is illustrated, but the species is not described since the shell is unknown. Both species feed on detached blades of the surfgrass Phyllospadix carried by turbidity currents into continental slope depths in the San Diego Trough. The anatomy of B. diegensis was investigated by means of semithin serial sectioning and graphic reconstruction. ‘The shell is limpet‐like; the protoconch resembles that of pseudococculinids and other lepetclloids. The radula is a distinctive, highly modified rhipidoglossate type with close similarities to the lepetellid radula. The anatomy falls well into the lepetelloid bauplan and is in general similar to that of Pseudococculinidae and Pyropcltidae. Apomorphic features are the presence of gill‐leaflets at both sides of the pallial roof (shared with certain pseudococculinids), the lack of jaws, and in particular many enigmatic pouches (bacterial chambers?) which open into the postcrior oesophagus. Autapomorphic characters of shell, radula and anatomy confirm the placement of Bathyphytophilus (with Aenigmabonus) in a distinct family, Bathyphytophilidac Moskalev, 1978. As revealed by a cladistic study, the Bathyphytophilidae should be classified within the Lepetelloidea close to the Lepetellidae, Pyropeltidae, and Pseudococculinidae.

The anatomy of Addisonia (Mollusca, Gastropoda)

SummaryThe organization of Addisonia lateralis (Requien, 1848) and A. brophyi McLean, 1985 is described. Addisonia species have a thin, asymmetrical, cup-like shell and a very simple shell muscle. Eyes, oral lappets and epipodial tentacles are absent and the right cephalic tentacle is also used as a copulatory organ. Most characteristic is the enormously developed gill which is enlarged into the right subpallial cavity. It is composed of about 30 leaflets with skeletal rods and its epithelia are uniquely arranged. The heart is large and the single auricle is situated anteriorly left. There are two kidneys: the left is small, while the right forms large coelomic cavities and has no connection with the pericardium or the hermaphroditic genital system. Testis and ovary are separate: both have a simple duct proper (vas deferens, oviduct). They are connected to the copulatory organ by an open seminal groove; a small receptaculum is present. The mouth opening is typically triangular, with no jaws or subradular sense organs. Addisonia possesses tuft-like salivary glands, a radula diverticulum and distinct, tubular oesophageal glands. The oesophagus itself is simple. The radula and the posterior alimentary tract are unique; the stomach is completely reduced and the intestine forms a pseudostomach. The streptoneurous, hyoathroid nervous system has pedal cords with three commissures. The visceral loop is also cord-like. A single (left) osphradium is present and the small statocysts have several statocones.The peculiarities and unique combination of primitive and advanced characters in Addisonia reflect a highly enigmatic organization among the Archaeogastropoda. Possible relationships to other archaeogastropod groups are discussed.

Anatomy and ultrastructure of the excretory system of a heart-bearing and a heart-less sacoglossan gastropod (Opisthobranchia, Sacoglossa)

Abstractu2002The microanatomy and ultrastructure of the excretory system of the Sacoglossa have been investigated from two species by means of semithin serial sections, reconstructions and transmission electron microscopy. Whereas Bosellia mimetica shows a functional metanephridial system consisting of a heart with ventricle and auricle in a pericardium and a single kidney, Alderia modesta lacks heart and pericardium, possessing only several haemocoelic sinuses and a very long kidney. In B. mimetica podocytes as the site of ultrafiltration could be detected in the pericardial epithelium lining the auricular wall. The flat epithelium of the kidney with extensive basal infoldings and a dense microvillous border towards the luminal surface serves to modify the ultrafiltrate. In A. modesta podocytes are absent. Solitary rhogocytes (pore cells), the fine structure of which strongly resembles podocytes (meandering slits with diaphragms covered by extracellular matrix), occur in B. mimetica and A. modesta, representing additional loci of ultrafiltration. The presence of podocytes situated in the epicardial wall of the auricle is regarded as plesiomorphic for the Mollusca and confirmed for the Sacoglossa in this study, contradicting earlier assumptions of the loss of the primary site of ultrafiltration in the ancestors of the Opisthobranchia. In contrast to the likewise heart-less Rhodopidae with a pseudoprotonephridial ultrafiltration system, A. modesta shows no further modifications of the excretory system.

Development of the excretory system in the polyplacophoran mollusc, Lepidochitona corrugata: The protonephridium

A single pair of protonephridia is the typical larval excretory organ of molluscs. Their presence in postlarval developmental stages was discovered only recently. We found that the protonephridia of the polyplacophoran mollusc, Lepidochitona corrugata, achieve their most elaborate differentiation and become largest during the postlarval period. This study describes the protonephridia of L. corrugata using light and electron microscopy and interactive three‐dimensional visualization. We focus on the postlarval developmental period, in which the protonephridia consist of three parts: the terminal part with the ultrafiltration sites at the distal end, the voluminous protonephridial kidney, and the efferent nephroduct leading to the nephropore. The ultrafiltration sites show filtration slits between regularly arranged thin pedicles. The ciliary flame originates from both the terminal cell and the duct cells of the terminal portion. The efferent duct also shows ciliation. The most conspicuous structures, the protonephridial kidneys, are voluminous swellings composed of reabsorptive cells (“nephrocytes”). These cells exhibit strong vacuolization and an infolding system increasing the basal surface. The protonephridial kidneys, previously not reported at such a level of organization in molluscs, strikingly resemble (metanephridial) kidneys of adult molluscan excretory systems. J. Morphol., 2011.

The protonephridial system of the tusk shell, Antalis entalis (Mollusca, Scaphopoda)

Abstractu2002The development and microanatomy of the protonephridial system in larvae and postmetamorphic juveniles of Antalis entalis (Dentaliidae) have been examined by means of a semithin serial sectioning and reconstruction technique. One late larval stage has been additionally examined by transmission electron microscopy. The protonephridium appears during larval development and is reduced in the juvenile approximately 13 days after metamorphosis. This is the first unambiguous evidence of a protonephridium in a postlarval mollusc. When fully developed the protonephridium is unique in consisting of two cells only, a terminal cell (=cyrtocyte) and a duct-releasing cell with glandular appearance. The polyciliary terminal cell has several distinct ultrafiltration sites, resembling conditions in bivalve protonephridia. The large duct-releasing cell shows a very large nucleus probably reflecting polyploidy. Its basal infoldings and many mitochondria suggest metabolic activity, the cytoplasm is characterised by many distinct granules. The unique features of the scaphopod protonephridial system are compared with available data on the protonephridia of other molluscan classes. The finding gives additional evidence that protonephridia belong to the ground pattern of the Mollusca.

Ultrastructure of the renopericardial complex in Hypselodoris tricolor (Gastropoda, Nudibranchia)

The histology and ultrastructure of the renopericardial complex of Hypselodoris tricolor (Gastropoda, Nudibranchia, Doridoidea) have been investigated by means of semithin serial sections and transmission electron microscopy (TEM). The examinations revealed a functional metanephridial system comprising a monotocardian heart with ventricle and auricle in a spacious pericardium that is linked with the single, large kidney by a renopericardial duct with prominent ciliation towards its opening. Podocytes as the site of ultrafiltration were not only detected in the auricular epicardium, but also line the entire outer pericardial epithelium. The cuboidal, highly vacuolated excretory cells of the kidney epithelium with extensive basal infoldings and an apical microvillous border indicate secretory and reabsorptive activity. Solitary rhogocytes (pore cells) of the connective tissue and haemocoel represent additional loci of ultrafiltration with a fine structure identical to that of the podocytes (slits between cytoplasmic processes, bridged by fine diaphragms and covered by extracellular matrix). The presence of podocytes situated in the epicardial wall of the auricle is regarded as plesiomorphic for the Mollusca and is confirmed for the Nudibranchia. An additional, extensive and separate ultrafiltration site in the outer pericardial wall is not known from any other taxon of the Mollusca and strongly suggests a significantly increased ultrafiltration activity in H. tricolor.