Coral preference behaviour by planktotrophic larvae of Spirobranchus giganteus corniculatus (Serpulidae: Polychaeta)

Planktonic larvae of the serpulid polychaete Spirobranchus giganteus, an obligate associate of live coral, were tested for preferences for materials diffusing from natural substrates. Choices offered were Acropora prolifera, a very abundant coral on the Heron Island reef flat; Palauastraea ramosa, a less abundant coral, dead coral rubble and a glass tube as a control. Larval life is approximately 12 days. The larvae tested were 1–4 days old. Adults of S. giganteus occur commonly on A. prolifera and much less frequently on P. ramosa. Experiments were designed to prevent contact between larvae and substrate. Larvae preferred A. prolifera over P. ramosa, rubble and the control. There was no preference expressed between the control and P. ramosa or the control and rubble. A preference by young S. giganteus larvae for a substance diffusing from coral, acting together with a known positive phototaxis, may be adaptive in that it may help to maintain larvae in surface waters over the reef and in the vicinity of a specific coral until they are old enough to settle.     

Effects of Ca2+ and catecholamines on swimming cilia of the trochophore larva of the polychaete Spirobranchus giganteus (Pallas)

Trochophore larvae of the tropical serpulid Spirobranchus giganteus (Pallas) swim by means of prototrochal and metatrochal rings of cilia. A system of developing neuntes carrying vesicles of several kinds is located on the inner surfaces of both prototrochal and metatrochal cells. The swimming cilia arrest on exposure to EDTA, Ba(OH)₂, lanthanum chloride, trifluoperazine and Ca²⁺ -free sea water, i.e. under conditions that interfere with the supply of external Ca²⁺. Swimming cilia are also arrested by the β-blocker alprenolol, an effect ameliorated by the α₁ agonist phenylephrine or the β agonist isoproterenol. We conclude that there is a Ca²⁺ -dependent, catecholaminergic excitation of the swimming cilia of the S. giganteus trochophore larva, involving β receptors and probably neurally mediated. Other cilia on the larval body are insensitive to the agents affecting the activity of swimming cilia.     

Serpulids (Polychaeta: Serpulidae) from the Northwestern Caribbean with keys to the Grand Caribbean region: Salmacina, Ficopomatus, Pomatoceros, Pomatostegus, Protula, Pseudovermilia, Spirobranchus and Vermiliopsis

From the revision of more than 1,250 serpulids, 15 species from the Grand Caribbean Region were identified and characterized. Thirteen species were collected along the shores of the Yucatan Peninsula and eight were found in other localities in the Gulf of Mexico, seven others are from Cuba and comments on type specimens of two species are also included. Three morphometric analyses were made to evaluate some characters. The first on Pomatostegus stellatus (Abildgaard), and related species and subspecies: P. brachysoma Schmarda, P. macrosoma Schmarda, P. s. fruticosa M?rch, P. s. pentapoma M?rch and P. s. tetrapoma M?rch, indicated that they are conspecific. Another one on Spirobranchus de Blainville species: S. dendropoma M?rch, S. giganteus (Pallas), S. polycerus (Schmarda) and S. polycerus augeneri ten Hove; indicated that S. giganteus differs from the other three taxa. The third analysis was made on Vermiliopsis annulata (Schmarda) sensu lato; it allowed the recognition of three different forms. Several incomplete specimens might belong to an undescribed genus. A key for identification of all the species recorded in the Grand Caribbean Region is also included.     

Aspects of the biology of Hyolitha (Mollusca)

Hyolitha constitute an extinct group of class rank assigned to Molhsca. Two orders, Ortho-thecida and Hyolithida, are well established and most knowledge of morphologic detail is derived from the latter. Both orders had an operculum not hinged to the conch. Hyolithida also had paired, curved, whiskerlike appendages, requiring complex musculature to move them and the operculum. The Hyolithida were probably deposit feeders living in shallow water, and accordingly were tentaculate. A reconstruction of the soft parts of this sedentary organism is given — a shallow mantle cavity on the dorsal side, anterior tentacles, a long intestine, and a reduced ventral foot. Except for the more complex musculature associated with an elaborate operculum, Orthothecida are judged to have had a similar anatomy.     

Ultrastructure of the eyespot in three polychaete trochophore larvae (Annelida)

Summary The eyespot is structurally similar in trochophore larvae of Harmothoe imbricata, Serpula vermicularis and Spirobranchus giganteus. In the receptor cell parallel lamellae lie below a tuft of microvilli which extends into a hollow in one side of the pigment cell. In 1-eyed trochophores this space connects with the outside via a small pore. In eyes preserved during the day there is evidence of a membrane breakdown in both lamellae and microvilli as well as indications of a membrane-fragment disposal system involving the receptor cell, the pigment cell and the eyespot pore. The orientation of the eyespot of S. giganteus is the reverse of that found in S. vermicularis, a situation that may be associated with ecologically significant differences in behaviour.     

Microstructure and formation of the calcareous operculum in Pyrgopolonctenactis and Spirobranchusgiganteus (Annelida, Serpulidae)

The calcareous operculum of Pyrgopolon ctenactis is composed of spherulitic prismatic structures. The opercular cup consists of regular spherulitic prismatic crystals; the talon has two layers, an inner with an irregular spherulitic prismatic structure (150 μm thick) and an outer with a regular spherulitic prismatic structure (110 μm thick). The outer regular structure has thick (1 μm) organic interprismatic sheets unique in biomineralization of this group, but similar to that of Bivalvia. We infer that control over biomineralization is stronger during the formation of the outer regular layer, with its thick organic interprismatic sheets, than during the formation of the inner irregular spherulitic prismatic structure, without such sheets. In Spirobranchus giganteus, opercular formation differs from that of P. ctenactis. S. giganteus has numerous pores in its opercular plate, and calcification starts with the formation of an outer irregularly oriented prismatic structure followed by an oriented prismatic structure without interprismatic sheets.     

Timing of development of the middle ear of Anura (Amphibia)

Summary The opercularis system and tympanum-stapes complex of the anuran middle ear develop at different times relative to metamorphosis. In early larvae, the fenestra ovalis is represented by a large lateral opening in the otic capsule filled with connective tissue. At later larval stages, but well before metamorphosis, a cartilaginous operculum begins to form at the posterior margin of the fenestra ovalis, and proceeds to expand to fill all except the anterior part of the fenestra. The opercularis muscle forms along with the levator scapulae superior muscle at the anteromedial edge of the developing suprascapular cartilage of the shoulder girdle. The muscle fibers extend anteroventrally towards the operculum and otic capsule, and, just before emergence of the forelimbs, that portion that will form the opercularis muscle inserts on the lateral surface of the operculum. At this stage, when the metamorphosing frogs first show terrestrial habits, the opercularis system is complete and presumably functional. Timing of development of the tympanum-stapes complex is more variable. The stapes begins as a cartilaginous condensation in the anterior part of the fenestra ovalis, and develops laterally to eventually contact the epidermis and dermis that together will form the tympanum. Meanwhile a middle ear cavity and tympanic annulus form to complete the complex. In several species, especially those that metamorphose at a smaller body size, the tympanum-stapes complex is quite incomplete by the end of metamorphosis, and in Hyla crucifer it takes about 60 days to fully develop. The presence of a complete opercularis system by the start of terrestrial activity is consistent with an hypothesized seismic function of the system. The independent timing of development of the opercularis system and tympanum-stapes complex does not support functional hypotheses linking the opercularis system with modulation of responsiveness of the tympanum-stapes complex to aerial sound. Newly metamorphosed frogs with poorly developed tympanum-stapes complexes are presumably either insensitive to aerial sound or employ alternate mechanisms for transmission of sound energy to the inner ear, possibly involving the opercularis system.     

Ultrastructure of Licea kleistobolus (Myxomycetes) and its bearing on the taxonomic affinity of the species

The peridium of Licea kleistobolus Martin consists of two distinct layers. Abundant refuse matter is evenly distributed on the surface of the fructification. The upper surface of the operculum is smooth and punctated by pores of variable size. The internal structure of the operculum is essentially the same as that of the peridium. Processes along the periphery of the lower surface of the operculum and along the upper edge of the sporangium function as an opening mechanism. The operculum bears hollow finger-like outgrowths and rounded warts, both being continuous with the inner wall of the operculum. The results of a SEM- and TEM-study indicate that the two different types of processes are homologous structures. Similarity between aberrant cap-illitial outgrowths along the margin of lobes in Listerella paradoxa Jahn and the processes bordering the sporangial edge and periphery of the operculum in L. kleistobolus , indicates affinity of the two species.     

Determination of the shape of the operculum by the bithorax complex in Drosophila melanogaster

Summary We have studied the course of the operculum line in the larval hypoderm of several bithorax complex mutants of Drosophila melanogaster. The bifurcation of the line, a characteristic of the first abdominal segment in wild-type (A₁), can also appear in the metathoracic (T₃) and other abdominal segments (A₂, A₃) depending on mutations within the bithorax complex. Therefore, we concluded that the course of the operculum line and thus the shape of the operculum is not determined by a suprasegmental gradient of positional information but by the functional state of the genes of the bithorax complex in each metamere. The dorsal and ventral branches of the operculum line react differently, the dorsal branch being more sensitive to the effect of loss of function mutations (bxd, iab-2 ^k), the ventral branch more affected by gain of function mutations (Hab). In some cases the effects of the mutations on the operculum line differed from those in the adult, suggesting a difference in sensitivity of larval hypodermal cells and histoblast cells to the functional gene products of the bithorax complex.     

Histochemical studies on the amphibian opercularis muscle (Amphibia)

Summary Histochemical studies of the opercularis muscle of the bullfrog (Rana catesbeiana) and the tiger salamander (Ambystoma tigrinum) provide evidence that the opercularis muscle of anurans is a specialized, tonic portion of the levator scapulae superior muscle. Staining results for myosin adenosine triphosphatase (ATPase) and succinate dehydrogenase (SDH), combined with measurements of muscle fiber diameters, demonstrate that the opercularis/levator scapulae superior muscle mass of both the tiger salamander and bullfrog consists of an anterior tonic portion, a middle fast oxidative-glycolytic (FOG) twitch portion, and a posterior fast-glycolytic (FG) twitch portion. In R. catesbeiana the tonic fibers represent 57.3% of the fiber total and (because they have relatively narrow diameters) about 29% of the cross-sectional area of the muscle mass, and form that part of the muscle (=opercularis muscle) that inserts on the operculum. In Ambystoma the tonic fibers represent only 8.8% of the fiber total and represent about 4% of the cross-sectional area. In the tiger salamander, the entire levator scapulae superior muscle inserts on the operculum and therefore represents the opercularis muscle. The bullfrog differs from the tiger salamander, therefore, in that the anterior tonic part of the opercularis/levator scapulae superior complex is greatly enlarged and the insertion on the operculum is limited to these tonic fibers. No evidence of a columellar muscle was found in R. catesbeiana. Previous reports of one in this species and in other anurans may be based on the tripartite nature of the opercularis/levator scapulae superior muscle mass. The middle FOG portion of the muscle may have been considered a muscle distinct from the anterior tonic portion (=opercularis muscle) and the posterior FG portion.     

Morphology and formation of the eggshell in the tarnished plant bug, Lygus lineloaris (Palisot de Beauvois) (Hemiptera: Miridae)

Scanning and transmission electron microscopy were used to study the morphology and formation of the eggshell in the tarnished plant bug, Lygus lineolaris. Eggs are bean-shaped, with an operculum at the anterior end surrounded by a row of 36-40 respiratory horns. Three micropylar openings are on the operculum, and are sealed in oviposited eggs. The chorion consists of the chorion proper and the innermost chorionic layer. An air layer composed of colonnades is present in the chorion. The innermost chorionic layer is homogeneous and electron lucent. The follicle cells secrete electron dense materials that later coalesced into the reticulated vitelline membrane. This is followed by the deposition of the innermost chorionic layer by the follicle cells. After the primordial innermost chorionic layer is formed, follicle cells at the anterior pole of the oocyte secrete the scaffold for the colonnades in the air layer. Later, the primordial scaffold matrix is redistributed and localized at the lateral and posterior end of the oocyte where it becomes secondarily modified. At the end of choriogenesis, follicle cells at the anterior pole secrete the operculum and respiratory horns.     

The opercular moult in Spirorbis spirorbis (L.) and S. pusilloides Bush (Polychaeta: Serpulidae)

Opercular moult has been examined in two spirorbids, the tube-incubating Spirorbis spirorbis (L.) and the opercular incubating Spirorbis pusilloides Bush. In both species epithelial ingrowth cuts off the old operculum and a new one differentiates on the proximal side of the constriction. The immediate fate of the severed tissues differs in the two species; in S. spirorbis the epithelia slowly wither as the platelike operculum finally breaks away by rupture of the cuticle while in S. pusilloides there is a cataclysmic autolysis of the epithelial tissues although the cuticle is retained and functions as an incubation chamber which ruptures at the close of incubation to release the larvae and is then shortly discarded.Opercular moult, rare in the immature animal in either species, normally begins with the onset of breeding. In S. pusilloides it is an essential preliminary to brooding and throughout the breeding season opercular moult rigidly alternates with brood incubation to produce a new incubation chamber for each successive brood. In S. spirorbis there is also some evidence of a partial correlation between brooding and opercular moult but the two events overlap and moulting is less frequent than the production of broods. A brief consideration is given to the evolution of the brooding habit and the tentative conclusion reached that opercular incubation has evolved twice in the Spirorbinae.     

Branchial placenta in the viviparous teleost Ilyodon whitei (Goodeidae)

Intraluminal gestation, as it occurs in viviparous goodeids, allows a wide diversity of embryo‐maternal metabolic exchanges. The branchial placenta occurs in embryos developing in intraluminal gestation when ovarian folds enter through the operculum, into the branchial chamber. The maternal ovarian folds may extend to the embryonic pharyngeal cavity. A branchial placenta has been observed in few viviparous teleosts, and there are not previous histological analyses. This study analysis the histological structure in the goodeid Ilyodon whitei. The moterno ovarian folds extend through the embryonic operculum and reach near the gills, occupying part of the branchial chamber. These folds extend also into the pharyngeal cavity. In some regions, the epithelia of the ovarian folds and embryo were in apposition, developing a placental structure in which, maternal and embryonic capillaries lie in close proximity. The maternal epithelium has desquamated cells which may enter through the branchial chamber to the pharyngeal cavity and the alimentary tract. The complex processes that occur in the ovaries of viviparous teleosts, and its diverse adaptations for viviparity, as the presence of branchial placenta, are relevant in the study of the evolution of vertebrate viviparity. J. Morphol. 275:1406–1417, 2014. © 2014 Wiley Periodicals, Inc.     

MINCHINIA CHITONIS (LANKESTER, 1885) LABBE, 1896, A HAPLOSPORIDIAN PARASITE OF THE CHITON, LEPIDOCHITONA CINEREUS

249 Lepidochitona cinereus were examined from different locationsalong the S.W., S., and S.E. coasts of the British Isles overthe last 12 years and the number infected with Minchinia chitonisrecorded. The spores, each with an operculum and two extensionsof the cytoplasmic envelope are described. The infection didnot appear to be limited to specific tissues, the digestivegland, muscles and gills all being invaded. It is suggestedthat the distribution of this parasite may have increased overthe past 50 years. (Received 3 January 1979;     

Mitogenomic phylogeny of the Naticidae (Gastropoda: Littorinimorpha) reveals monophyly of the Polinicinae

The Naticidae is a species-rich family of predatory marine gastropods with substantial interspecific morphological diversity. The classification of the Naticidae has been traditionally based on morphology data, but the phylogenetic relationships within the family are debated due to conflicting molecular results, especially regarding the monophyly of subfamilies Polinicinae and Naticinae. To further resolve the phylogenetic controversies within the Naticidae, we undertake a phylogenetic approach using 14 newly sequenced complete or nearly complete (only lacking a control region) mitochondrial genomes. Both the maximum likelihood and Bayesian inference analyses supported monophyly of the Polinicinae, but paraphyly of the Naticinae due to the placement of the enigmatic genus Notocochlis. The ancestral character reconstruction suggests that the operculum, a character that currently defines the two subfamilies, evolved from an ancestor with a calcareous operculum in the evolutionary history of naticids. In addition, the chronogram estimates that naticids was originated in late Triassic (about 227 million years ago), consistent with previous hypotheses. Our study highlights the importance of using complete mitochondrial genomes while reconstructing phylogenetic relationships within the Naticidae. The evolution scenario of the naticid operculum contributes new insights into the classification of Naticidae.     

Comparative morphology of the amphibian opercularis system: I. General design features and functional interpretation

The morphology of the opercularis system of anuran and caudate amphibians suggests that it acts to produce motion of the operculum that in turn produces fluid motion within the inner ear. The operculum and opercularis muscle form a lever system, with a narrow connection between the operculum and otic capsule acting as a fulcrum about which the operculum moves in response to forces applied via the muscle. The opercula of many species possess a muscular process on which the muscle inserts, thereby increasing the moment arm through which the muscle acts. The tonicity of the opercularis muscle allows tensile forces produced by substrate vibration or other mechanical energy applied to the forelimb to be effectively transmitted to the operculum; the elasticity of the connective tissue holding the operculum in place should act to return the operculum to its original position. The opercularis systems of frogs and non-plethodontid salamanders are similar structurally and functionally; that of plethodontid salamanders is structurally distinct but also functions as a lever system. Fluid motion produced by opercular motion could stimulate various end organs of the inner ear; the saccule, lagena, and amphibian papilla are in close approximation and wave energy could directly affect their otoconial or tectorial structures. In those anurans with a tympanic ear, the stapedial footplate and operculum articulate, but this articulation allows both to move independently. The stapes-tympanum complex and opercularis system therefore appear to be independent functional systems, and it is unlikely that the opercularis system modulates middle ear responsiveness. The general design of the opercularis system is consistent with a function in reception of substrate vibrations.     

Internal morphology of two species of Lagenochitina (Chitinozoa)

Internal and external structures of Lagenochitina boja Bockelie 1980 and L. esthonica Eisenack 1955 have been examined with a scanning electron microscope. The material derives from limestone samples from the Arenig to ?Lower Llanvirn succession of NE Spitsbergen. The species possesses both an operculum and a prosoma (Bockelie, 1978). The operculum, in the shape of a thin flat disc, closes the aperture of the test. A cylindroconical structure is enclosed in the test aborally of the operculum. the cylindrical part of this structure, the prosoma, is transversed by numerous thin disc-shaped laminae. The sequence of thin laminae is terminated in a thicker lamina, here termed the subex. The prosoma wall is extended aborally forming a conical structure, the rica. The prosomai of individual specimens show variation in length, microstructures and the attachment to the test. The internal structures of Lagenochitina species are compared with similar structures known from other chitinozoan species.     

Perianth development inAngophora and the bloodwood Eucalypts (Myrtaceae)

The petals ofAngophora flowers are compound structures consisting of two morphologically distinct components that develop along separate morphogenetic pathways. These two components are also evident in the corolline parts of the bloodwood eucalypts. In occasional flowers ofAngophora and some bloodwoods, several adjacent corolline primordia may become continuous due to interprimordial growth, but the petals are mostly free at anthesis. In other bloodwood eucalypt species all the primordia in the corolline whorl become continuous at some stage in development, resulting in an operculum that is anatomically unresolvable into its original petaline parts. The varying degrees of this continuity that are evident within individual trees (and even within single flowers) suggests that operculum formation is an epigenetic event that is determined by morphogenetic processes within the flower. It is suggested that these may relate to differing rates of growth in different regions of the bud.