STRUCTURE OF THE CONCHIOLIN CASES OF THE PRISMS IN MYTILUS EDULIS LINNE

The prisms in the shell of Mytilus edulis Linné are calcite needles. Their small size and their thin conchiolin cases distinguish them from the prisms of many other species of mollusks. These Mytilus prisms have been studied with the electron microscope. The material consisted of positive replicas of surfaces of the prismatic layer, etched with chelating agents, and of preparations of tubular cases from decalcified prisms which were compared with the conchiolin from decalcified mother-of-pearl of the same species. In the replicas, the cases appear as thin pellicles in the intervals between the prism crystals. Both the prism cases and the nacreous conchiolin, disintegrated by exposure to ultrasonic waves and sedimented on supporting films, appear in the form of tightly meshed, reticulated sheets, described as "tight pelecypod pattern" in former studies on nacreous conchiolin of Mytilus. The results show that in the shell of this species the same conchiolin structure is associated with aragonite in mother-of-pearl and with calcite in the prismatic layer.     

THE SETTLEMENT OF POST LARVAL MYTILUS EDULIS (SETTLEMENT OF POST LARVAL MUSSELS)

It is probable that post larval mussels cut their byssus moorings.For those that gain their freedom in this way, two modes ofpassive flotation are possible. In the ‘summer’mode, they are lifted into the water column on the end of amucus filament; in the ‘winter’ mode, they attachthemselves to certain negatively buoyant debris which leavesthe bottom when the tide flows. Passive flotation prolongs the errant existence of post larvalmussels by increasing their drag. By enabling them to avoidsilt and keep in touch with hard substrates, passive flotationmakes it more likely that they will settle advantageously. The two modes of passive flotation pose an all-the-year-roundthreat of fouling to the cooling water systems of coastal powerstations. (Received 27 April 1982;     

COMPARATIVE ANALYSIS OF KARYOTYPES AND NUCLEOLAR ORGANIZER REGIONS IN DIFFERENT POPULATIONS OF MYTILUS TROSSULUS, MYTILUS EDULIS AND MYTILUS GALLOPROVINCIALIS

The cylotaxonomical characteristics of Mytilus tros-sulus, M.edulis and M. galloprovincialis were studied using karyometricanalysis and silver staining. The karyotype of M. trossulus,reported here for the first time, consists of six metacentricand eight submetacentric-subtelocentric chromosome pairs. Theoccurrence of five metacentric chromosome pairs in M. galloprovincialisdifferentiates this taxon from M. trossulus and M. edulis whichboth have six meta-centrics. The number of submetacentric tosubtelo-centric chromosome pairs was variable between populationsand between taxa. We suggest that this variability has arisenfrom differential chromosome condensation rather than from structuralchange. Intercomparison of chromosome relative length showedstrong similarity among the three taxa. Chromosomal nucleolarorganizer regions (NORs) were identically located on two submetacentric-subtelocentricchromosome pairs in all three taxa. However, M. trossulus showeda characteristic difference in the occurrence of NORs on onemetacentric pair, which was absent in M. galloprovincialis andM. edulis. Variability in the number of NORs per cell was observedin all populations studied. We conclude that the three taxaof Mytilus studied here cannot be differentiated by asinglekaryological character, but that a combination of karyologicalcharacters is virtually diagnostic ^* To whom correspondence should be sent (Received 24 January 1994; accepted 9 March 1994)     

EXCLUSION OF THE ROLE OF SECONDARY CONTACT IN AN ALLELE FREQUENCY CLINE IN THE MUSSEL MYTILUS EDULIS

We examined the hypothesis that secondary contact generates an allele-frequency cline at the aminopeptidase-I locus (Lap) in the marine mussel, Mytilus edulis. It has been proposed that variation at the Lap locus is neutral and that the cline results from secondary contact between differentiated oceanic and estuarine populations (Levinton, 1980). We tested this hypothesis by comparing the genotypic distributions in samples from the cline to distributions that incorporate mixing effects. We employed a statistical model that determines the degree of contact using a maximum likelihood estimator and then incorporates the mixing estimates into an expected distribution of genotypes. Wahlund effects resulting from possible admixture are thereby incorporated into the expected distribution. Failure of the model to reconcile the observed with the expected distribution of genotypes indicates that the observed population structure does not result from admixture. The null hypothesis of mixing was unable to explain about 33% of the samples. Combined tests demonstrated the general departure from the mixing model to be highly significant. The distribution of heterozygote discrepancies across the cline was inconsistent with the expectations of a mixing model. Therefore we reject explanations for the structure of the Lap cline that involve secondary contact. Selection directed at the Lap locus appears necessary to explain the genotypic structure of clinal populations.     

SOME ECOLOGICAL ASPECTS OF THE FEEDING BEHAVIOUR OF THE OYSTERCATCHER HAEMATOPUS OSTRALEGUS ON THE EDIBLE MUSSEL MYTILUS EDULIS

Oystercatchers have two methods of opening mussels, both neatly adapted to the structure of the prey. To open mussels exposed by the tide, the bird hammers a hole along the ventral margin of the shell, whereas to open mussels under water, the bird drives its bill into the gape of the valves to cut through the posterior adductor muscle. Large and strong-shelled mussels can be opened by stabbing but not by hammering. Feeding methods of Oystercatchers vary from mussel-bed to mussel-bed. These variations in behaviour are attributable to differences in the strength of the shells of the prey and to the firmness of their attachment to the substrate. Diversity of ecological conditions on the mussel-beds causes an apparent size selection of prey by Oystercatchera.     

THE INFESTATION OF MYTILUS EDULIS LINNAEUS BY POLYDORA CILIATA (JOHNSTON) IN THE CONWY ESTUARY, NORTH WALES

The incidence of the shell-boring parasite Polydora ciliatain Mytilus edulis from the Conwy estuary, North Wales is described.Amongst mussels >40 mm in shell length both the occurrenceand abundance of P. ciliata increased steeply with host size.Infestation was highest amongst mussels near the mouth of theestuary where around 60–65% of the population was parasitized;no systematic relationship between the incidence of P. ciliataand tidal elevation was observed. Mussel condition was negativelycorrelated with the degree of infestation. Moderately and heavilyinfested mussels, however, never accounted for more than ca.10% of this population and the overall detrimental effects ofP. ciliata on growth and production is thus probably quite small.Whilst heavily infested mussels were evidently more vulnerableto predation, the shore crab, Carcinus maenas, selected smaller,non-infested mussels whenever these were available. No obviousrelationships were found between the presence of P. ciliataand the incidence of either pearls or pea crabs. (Received 14 January 1991; accepted 2 April 1991)     

SPATIAL VARIATION IN THE FAUNA ASSOCIATED WITH MYTILUS EDULIS ON A WAVE-EXPOSED ROCKY SHORE

The fauna associated with Mytilus edulis at a rocky wave-exposedlocality in North Wales is reported. A total of fifty-nine taxawith representatives from most of the main invertebrate phylawas recorded. In terms of species richness the community wasdominated by crustaceans (25 taxa), molluscs (10 taxa) and cheliceratearthropods (9 taxa), mainly mites. Fora-miniferans and crustaceanswere the most abundant taxa, representing 25% and 23% of thetotal associated fauna respectively. Nemerteans and nema-todeswere also well represented. The mussel bed was broadly stratifiedinto three distinct layers each dominated by a single species.Thus, the foramini-feran Ammonia batavus was restricted to thesediment in the bottom layer, the barnacle Semibalanus balanoidesoccurred only on the outer exposed surfaces of the mussel shells,whilst the tiny brooding bivalve, Lasaea rubra, nestled mainlyamongst the complex matrix of byssal threads and shell fragmentsin the middle layer of the bed. Species richness and diversitydecreased systematically with tidal elevation and both theseindices were also signifocantly depressed amongst mussel communitiesfrom high-shore tide pools. Inclination of the rock surfacehad little or no effect on the mussel populations or their associatedfauna. Small mussel patches generally supported fewer taxa perunit area and had a lower diversity than larger, more extensivepatches. These marked, small-scale spatial variations exhibitedby the fauna associated with M. edulis appear to be relatedlargely to the degree of aerial and tidal exposure, mussel density,the amount of accumulated sediment and mussel patch size. (Received 2 August 1993; accepted 8 November 1993)     

A PLANIMETRIC STUDY OF MORPHOLOGICAL VARIABILITY IN THE DIGESTIVE DIVERTICULA OF LITTORINA LITTOREA (LINNAEUS) AND MYTILUS EDULIS LINNAEUS

The inter-and intratubular morphological variability in thedigestive diverticula of Littorina littorea and Mytilus edulishas been investigated by planimetric procedures. Five parametershave been measured: mean epithelial thickness (MET), mean diverticularradius [MDR], mean luminal radius (MLR), MLR/MET ratio and MET/MDRratio. The results indicate that irrespective of the patternof tubule organization within the digestive diverticula (whethertubule types are clustered or not), variability between individualsis greater than that between zones of the digestive gland. Thishas implications for the design of sampling strategies in investigationsof the morphology of digestive diverticula in physiologicaland pathological studies. The variability in the epithelialthickness within diverticular sections is of minor relevancein assessing the overall condition of the digestive gland inthese studies, because variability in epithelial thickness betweentubules is significantly greater than within tubules in bothspecies. (Received 10 March 1989; accepted 16 October 1989)     

THE ACROSOME REACTION IN MYTILUS EDULIS : I. Fine Structure of the Intact Acrosome

The intact acrosome of the Mytilus edulis spermatozoon consists of a conical vesicle, the basal side of which is deeply invaginated so that the whole vesicle forms a sheath around a very slender axial rod, about 2.7 µ long, inserted in a tube passing through the nucleus. The annular base of the acrosomal vesical is filled with a homogeneous substance; the outer wall of the vesicle is lined with a somewhat irregular layer of a particulate substance interspersed with very fine tubular elements, and its lumen is nearly filled by a strand of material which extends from the inner tip of the invagination to the apex of the acrosome. The lumen of the invagination appears empty except for the rod and a delicate sleeve-like structure which surrounds it. The plasma membrane of the sperm cell lies in immediate contact with the acrosomal membrane over its whole outer surface. In its general organization, this molluscan acrosome shows a rather close homology with that of the annelid Hydroides.     

FINE STRUCTURE OF THE CILIA OF ROTIFERS

The fine structure of the coronal cilia of the rotifer Philodina citrina has been studied in detail. Specimens were fixed with OsO₄ and embedded in butyl—methyl methacrylate, Epon 812, or Vestopal and sectioned with a Porter-Blum microtome. The details of structure of the rootlets, basal bodies, basal plates, and free cilia are described. The general structure of the rotifer ciliary apparatus conforms well to that established for other species. One of the main observations is the difference in structure of the peripheral filaments in the opposing halves of a cross-section of the free cilium. Also, in longitudinal sections evidence is offered for the existence of a helical structure in the peripheral filaments.     

SOME PROPERTIES OF THE PROTEIN FORMING THE OUTER FIBERS OF CILIA

Cilia were isolated from Tetrahymena pyriformis by an ethanol-calcium procedure. Solutions of outer-fiber protein were obtained either by aqueous extraction of an acetone powder of whole cilia, or by dissolving the isolated outer-fibers in 0.6 M KCl. In aqueous solution, the outer-fiber protein has a sedimentation coefficient of 6.0S and a molecular weight of 104,000 ± 14,000. In 5 M guanidine hydrochloride solution the molecular weight falls to 55,000 ± 5,000. After reduction and alkylation in 8 M urea, about 95% of the protein migrates as a single band on electrophoresis in polyacrylamide gel at pH 8.9; the migration velocity is identical with that of reduced and alkylated actin. Freshly prepared outer-fiber protein contains about 7.5 sulfhydryl groups per 55,000 g of protein. The amino acid composition of outer-fiber protein resembles that of actin, with such differences as occur being of the same order as those between actins from different species of animal.     

THE REGENERATION OF CILIA IN PARTIALLY DECILIATED TETRAHYMENA

Partial deciliation of Tetrahymena resulted in cells losing 75% of their cilia, with the balance being paralyzed. The paralyzed cilia are resorbed in the first 20 min after partial deciliation, and regeneration of cilia begins before resorption is completed. Inhibition of protein synthesis with cycloheximide does not inhibit ciliary resorption or regeneration, whereas vinblastine sulfate inhibits regeneration but not resorption. Inhibition of regeneration occurs in completely deciliated cells when they are treated with cyclohexmimide or vinblastine sulfate. It is concluded that the resorbing cilia contribute materials which allow regeneration to occur in the absence of protein synthesis. The volume of cilia regenerated in the presence of cycloheximide in partially deciliated cells is greater than the ciliary volume which is resorbed. This suggests the Tetrahymena cells have a pool of ciliary precursors. This pool does not contribute materials for regeneration in completely deciliated cells which are treated with cycloheximide. It is concluded that resorbing cilia in partially deciliated cells contribute materials which potentiate assembly of cilia from the pool of precursors.     

毛竹地下茎对创伤的反应

研究了在中国最为广泛栽培的毛竹(Phyllostachys edulis(Cart.)H.de Lehaie)的地下茎的创伤反应。创伤后的第1天,在伤口附近没有明显反应;2d之后,创口附近可以观察到生理反应的代谢物,在后生木质部的导管中以及在基本组织细胞的胞间隙出现粘状物质,这些粘状物质具有果胶特性;创伤后1周,创口附近的筛管及基本组织中的短细胞的细胞壁变成木质化。同时,基本组织中的长细胞的内壁出现新的次生壁的沉积;2周后,创伤反应的组织与未受创伤的组织之间的区别变得更加明显;4周后,一些导管完全充满了粘性物质,但没有观察到侵填体。由于细胞壁的木质化及酚类物质的填充,筛管完全失去了功能。对创伤后6周的材料进行观察的结果表明,其创伤反应的范围不再扩展,在创伤组织与未受伤组织之间的基本组织的细胞壁变得相当厚,从而在两者之间形成一道屏障。毛竹地下茎的这种创伤反应与毛竹竹竿的创伤反应基本上是一致的,只是略有不同。     

DIRECT FLUORESCENT ANTIBODY-DIRECT VIABLE COUNT AND POLYMERASE CHAIN REACTION DETECTION LIMIT FOR THE IDENTIFICATION OF VIBRIO CHOLERAE O1 IN MUSSELS (MYTILUS EDULIS)

Vibrio cholerae O1 is natural to the aquatic environment and can cause gastrointestinal infections when it is consumed from contaminated bivalves. Under unfavorable conditions, this bacterium enters into a viable but nonculturable state. Immunofluorescence and polymerase chain reaction (PCR) methods were a useful alternative for detecting this microorganism without a pre-enrichment step. We investigated the detection limit of the direct fluorescent antibody (DFA)-direct viable count (DVC) and PCR techniques for the identification of V. cholerae O1 in mussel ( Mytilus edulis ) samples. When 10³ cfu/mL V. cholerae O1 were inoculated in samples, 10²–10³ bacteria mL⁻¹ were determined by immunofluorescence tests and 67% of the samples were positive by PCR assay. No significant difference ( T statistic value = 6.5, P =  0.2049) between DFA and DFA-DVC procedures was observed. No presence of endogenous V. cholerae O1 was detected .

PRACTICAL APPLICATIONS

Vibrios are considered the major cause of identifiable illness and death from shellfish consumption. In Argentina, the viable but nonculturable (VBNC) forms of Vibrio cholerae O1 were identified in samples of water and plankton. Because of these facts, it is relevant to research the presence of V. cholerae O1 in aquatic bivalves. Immunofluorescence and polymerase chain reaction methods are a useful alternative to traditional enrichment testing for detecting both culturable and VBNC forms of V. cholerae O1. In this work, it was demonstrated that these methods were sensitive and efficient for detecting V. cholerae O1 in mussels without a pre-enrichment step. Moreover, they can be a useful tool for the rapid detection of this pathogen in the seafood industry.