The cyphonautes larva found in certain ectoproct Polyzoa is considered to be most probably a primitive larval form, which has been lost in viviparous species, the larvae of which are degenerate in varying degree and settle within a short time. The cyphonautes is truly planktonic and has a free swimming Life of some length—of 2 months according to Marcus (1940, p. 334)—and unlike the other known larvae of the group, has a functional alimentary canal. It obtains its food by maintaining a continuous current of water through the mantle cavity or vestibule, its ciliary mechanism being organized on a plan somewhat resembling that of bivalve molluscs, with an inhalant and an exhalant chamber with interposed ciliary ridges bearing current-producing and food-conveying cilia. As in lamellibranchs the organ creating the water and food currents is separated by a considerable interval from the mouth. In lamellibranchs this interval is bridged by the palps and the oral grooves; in the cyphonautes by the ciliated tract of the funnel. The cyphonautes being a larval form of probably archaic character its method of feeding is of particular interest.

Generation of ion electrochemical potential differences by primary active transport can involve energy inputs from light, from exergonic redox reactions and from exergonic ATP hydrolysis. These electrochemical potential differences are important for homoeostasis, for signalling, and for energizing nutrient influx. The three main ions involved are H+, Na+ (efflux) and Cl− (influx). In prokaryotes, fluxes of all three of these ions are energized by ion-pumping rhodopsins, with one archaeal rhodopsin pumping H+into the cells; among eukaryotes there is also an H+ influx rhodopsin in Acetabularia and (probably) H+ efflux in diatoms. Bacteriochlorophyll-based photoreactions export H+ from the cytosol in some anoxygenic photosynthetic bacteria, but chlorophyll-based photoreactions in marine cyanobacteria do not lead to export of H+. Exergonic redox reactions export H+ and Na+ in photosynthetic bacteria, and possibly H+ in eukaryotic algae. P-type H+- and/or Na+-ATPases occur in almost all of the photosynthetic marine organisms examined. P-type H+-efflux ATPases occur in charophycean marine algae and flowering plants whereas P-type Na+-ATPases predominate in other marine green algae and non-green algae, possibly with H+-ATPases in some cases. An F-type Cl−-ATPase is known to occur in Acetabularia. Some assignments, on the basis of genomic evidence, of P-type ATPases to H+ or Na+ as the pumped ion are inconclusive.

In October 1991, invertebrate larvae abundances were analysed to study the influence of the disturbance of the Canary Current flow by the Canary Islands archipelago on the variability of larval distribution. Two transects and two time-series stations located to the north (non-perturbed zone) and the south (perturbed zone) of the Canary Islands were sampled. Oceanographical data showed a highly stratified water column and zonally uniform salinity and temperature seaward of the African upwelling in the non-perturbed zone, while the perturbed zone presented strong turbulence in the form of mesoscale eddies. Invertebrate larval abundances were lower for most taxa studied in the non-perturbed zone and northern time-series station. Significant differences (P < 0.001) of invertebrate larval abundance between the two zones sampled were found. Decapod larvae were the most abundant larval group in both zones. Stations located in eddy structures presented the highest values of larval densities. Specifically, the larvae collected at Station 18, located in the core of an anticyclonic eddy, represented 60±18% of total larvae collected in the south transect. Finally, our results suggest that eddies, mainly anticyclonic eddies, act as a strong larval retention zone south of the islands, and that there is a local northward transport from the Canary Islands.

In the present study a comparison of the otolith morphology of two species of parrotfish, family Scaridae, collected from the Red Sea coast of Egypt, is conducted to identify the most appropriate taxonomic characters that separate these species. Ontogenetic changes in the otoliths of the two scarid fishes become evident. In the otoliths of Chlorurus sordidus, the following characters are comparable in small-sized adult fishes: otolith width, otolith depth, mesial surface shape, lateral surface shape, shape of sulcus acusticus, column, rostrum and size of rostrum. The otoliths of young adults (GI) C. sordidus differ from the adult ones in 14 out of the 22 characteristics studied. In the otoliths of Hipposcarus harid, the following characters are comparable in small and large fish: otolith width, otolith depth, mesial and lateral surface shapes, shape of sulcus acusticus, rostrum and size of rostrum.

Jørgensen (1944) showed that young specimens of the siliceous freshwater sponge Spongilla lacustris L. obtained their skeletal silica from the water and demonstrated that, under experimental conditions, a relationship existed between the size of the microscleric spicules produced and the concentration of dissolved silicate in the culture medium. The thickness of the microscleres increased with increasing concentration of dissolved silicate in the medium but no changes were detected in the lengths of the microscleres or in the size of the megascleres. Prior to this report Jewell (1935) showed that specimens of 5. lacustris with normal spiculation were rarely found in natural waters with a silicate content below 0.005 to 0.01 mm Si02. Hartman (1958) suggested that the greater thickness of siliceous spicules found in specimens of Haliclona caniculata Hartman collected in winter from New England shores, compared with spicules from summer-collected specimens, might reflect the increased concentration of dissolved silicate in the sea water during the winter months. Similar effects have been demonstrated experimentally in calcareous sponges: Maas (1906) showed that calcareous sponge larvae reared in calcium-free water produced no mineral spicules but organic ‘spiculoids’ of similar form. A relationship between spicule size and environmental silicate has not, in the past, been conclusively demonstrated for any siliceous sponge in field conditions.

Carlisle (1954) described Styela mammiculata, a new species of stalked ascidian from the Plymouth area, and suggested that it had been brought into British waters, probably with oysters. Its recent discovery on other parts of the south coast of England (Houghton & Millar, 1960) supports the idea that it is an introduced species which is now spreading through a favourable environment. It is well, therefore, to consider whether this may not be a species known from another part of the world. Tokioka (1955) examined one of Carlisle's specimens and suggested that it fell within the range of variation of S. clava Herdman. As many specimens of S.mammiculata are now available, a more extensive comparison has been made and is reported in this paper.

Growth of shells of larvae of Nassarius reticulatus (L.) and Crepidula fornicata (L.) reared in the laboratory under constant temperature (14 °C) and illumination (155 lx) occurs by the addition of successive strips secreted at the mantle edge. Growth lines on the embryonic teloconch also indicate intermittent growth; the protoconch secreted by the shell gland has no such lines. There is evidence that growth periods are short and pauses separating them prolonged. The diameter of the older whorls of the shells of these and six other species examined increase with the volume of the viscera. This change in diameter is made possible by the flexibility of the organic matrix, the funda-mental constituent of the shell. The matrix, secreted as fibres at the mantle edge, forms sheets, and provides sites for the deposition of calcareous concretions; at metamorphosis the concretions apparently initiate the formation of crystals. The concretions also sculpture the surface of the shell producing a pattern sufficiently conspicuous to allow identification of some species with the aid of only the stereomicroscope. For example, large concretions form longitudinal rows over the protoconch and teloconch of Littorina neritoides (L.) and smaller ones combine to form a more decorative pattern in Rissoa sarsi Loven. In other species details of the surface design require a scanning electron micro-scope. Interspecific differences in the arrangement of concretions may be traceable to differences in the pallial glands which secrete the matrix.

The reproductive biology of two epizoic deep-sea anemones reveals contrasting reproductive strategies. Amphianthus inornata (Cnidaria: Anthozoa) lives attached to the bathyal gorgonian Acanella arbuscula (Cnidaria: Anthozoa). Females of A. inornata increase in wet body weight as a result of increased oocyte production until 40% of the body weight is reproductive tissue. The anemone reproduces on a seasonal basis, releasing eggs in the early spring of each year. By contrast, Kadosactis commensalis (Cnidaria: Anthozoa) lives attached to the body wall of the abyssal holothurian Paroriza prouhoi (Echinodermata: Holothurioidea). This anemone is a protandric hermaphrodite, females being found only at the anterior end of the holothurian, whilst males are found at any point on the host. Females have a significantly higher wet weight than males and neither sex shows any reproductive seasonality.

The stomach is the principal region of extracellular digestion in the alimentary tract of Ciona intestinalis (L.) (Yonge, 1925; Morton, 1960). The region is oval and has a lining epithelium thrown into 30 or 40 longitudinal ridges. Previous authors have described the following cell types in this gastric epithelium: a mucous cell (Roule, 1884; van Weel, 1940); an un-differentiated cell (Yonge, 1925; Millar, 1953; Fouque, 1954); an absorptive cell (Yonge, 1925; Berrill, 1929; van Weel, 1940; Morton, 1960); a storage cell (Yonge, 1925; van Weel, 1940) and several different secretory cells (Roule, 1884; Yonge, 1925; Berrill, 1929; van Weel, 1940; Millar, 1953; Fouque, 1954; Morton, 1960). The present paper reports a re-investigation of the gastric epithelium by histochemical methods and by electron microscopy, and a comparison of the observations with those of previous authors. The fine structure of the gastric cells is compared with that of cell types in the ‘liver’ of Pyuridae (Degail & Lévi, 1964) and in the alimentary tract of other animals.

A new species of Hirondellea was trapped in large numbers (N=441) in the Atacama Trench (Pacific Ocean) at 7800 m depth. The species accounted for 47% of the total number of amphipods collected and was the second most abundant amphipod after Eurythenes gryllus. Adult males and females reached maximum lengths of 13·5 and 14·1 mm. Length–frequency histograms showed no clear evidence of growth classes, but instars could be determined by using a combination of morphological criteria and size–frequency data. Growth factors based on mean lengths of successive instars ranged from 1·09 to 1·24 except at moults immediately prior to maturity when factors were in the range 1·02–1·04. Females moult from the pre-adult to the adult instar, without body growth. Moulting modalities of immature males are unclear. Equations obtained from regression analysis between wet weight and total body length indicate an allometric growth. Females grow at a rate of 10% higher than males, and both females and males display growth rates lower than those observed for juveniles, but growth increments at each instar of females are not significantly higher than those of males. The relationship between total body length (L) and wet weight (W) of all instars of Hirondellea sp. nov. is expressed by the power curve W=0·012 L3·279 (W in mg and L in mm).

This study reports the morphometric relationships and relative growth of 20 uncommon bivalve species collected along the Algarve coast (southern Portugal). Morphometric relationships were established between three linear variables (shell length, height and width) and one ponderal variable (total weight) and the relative growth between variables (isometry vs allometry) was analysed in order to assess their variation throughout ontogeny. In addition, morphometric indices (elongation, compactness, convexity and density) based on ratios of those linear and ponderal variables were calculated in order to further characterize morphologically the bivalve species. A total of 2512 individuals belonging to nine bivalve families were analysed, comprising specimens with broad ranges in both shell length (11.8–109.0 mm SL) and total weight (0.2–354.6 g TW). All morphometric relationships were highly significant (P < 0.001) and displayed invariably high correlation coefficients (r = 0.727–0.998). Among a total of 60 morphometric relationships, 27 isometries, 25 positive allometries and 8 negative allometries were registered. The morphometric indices displayed a remarkable variation among taxa, reflecting the high morphological diversity of these miscellaneous bivalve species. Discriminant analysis provided a spatial visualization of the species morphometric variables that further evidenced their main shape features, the distinctness between some species and families (e.g. Pharidae and Cardiidae) and the morphological resemblance among some species belonging to other families (e.g. Veneridae and Tellinidae). Overall, this information is useful and has practical application in diverse research fields, including studies on systematics and taxonomy, physiology, biology, ecology, fisheries assessment and management.

Paraphysomonas cribosa n.sp. possesses two unequal flagella, one short and smooth, the other long, bearing numerous fine hairs. The cell surface is covered with scales which are resolvable using the electron microscope. These are polymorphic, built of rods and generally having an oval periphery. Struts from this support an inner oval ring, and further struts support a central perforated area.

The relationships between the standing stocks of deposit-feeding benthic invertebrates and benthic chlorophyll-a, phaeopigment and total combustible organic matter were investigated at a series of coastal lagoons and in the type of intertidal soft-sediment sites from which the lagoons originated. Across all the sites, in Norfolk, UK, an inverse relationship occurred between (a) the amounts of chlorophyll-a and of other potential food materials and (b) the degree of coverage by water. The biomass of consumers also decreased with increased water coverage, so that the lagoons supported less biomass than the adjacent high-level intertidal sites. Further, the deposit-feeder biomass supported by unit food decreased with extent of water coverage.

There was no evidence of any relationship between deposit-feeder and food biomass within any single site, in spite of the study period being selected to be that in which there was maximum likelihood of competition for microphytobenthic food. Whilst chlorophyll concentrations may set the maximum achievable level of consumer biomass at these sites, including in the deeper lagoons setting very low potential maximum population densities, the seasonal abundance patterns of the deposit feeders appear to be determined by other factor(s).

Expected lifetime investment in eggs and related parameters are described for a lagoonal population of Hydrobia ventrosa (Mollusca: Gastropoda) in East Anglia, UK, and these are compared with those of East Anglian lagoonal populations of H. neglecta and both lagoonal and intertidal-marine populations of H. ulvae. In contrast to an earlier study on Danish populations, which suggested that H. neglecta and H. ventrosa are at opposite ends of the hydrobiid spectrum of investment in reproduction, the order of increasing relative allocation of resources to egg production runs H. neglecta = H. ventrosa → lagoonal H. ulvae → intertidal-marine H. ulvae. That is, from the two small, short-lived, specialist lagoonal species producing few, large, directly-developing eggs, to the larger, potentially longer-lived H. ulvae that produces many small eggs which develop into veliger larvae. The lagoonal populations of all three Hydrobia species, however, are very similar to each other in terms of reproductive investment. When like cohorts are compared, in each, the annual egg weight is equal to the annual adult growth increment, and the weight of eggs produced per expected lifetime is half the adult growth increment at the time of death. These lagoonal populations are markedly dissimilar to intertidal-marine populations of H. ulvae, which produce an annual weight of eggs some 15 times the annual adult growth increment, and an expected lifetime egg weight some two-and-a-half times the adult growth increment at the time of death.

A 6·1-m long female basking shark (Cetorhinus maximus) was tagged 73 km east of Nantucket Island, Massachusetts on 27 September 2001 with a pop-up archival transmitting tag. The tag detached prematurely on 6 December 2001 in an area approximately 800 km south-west of the tag site off the coast of North Carolina. The basking shark was vertically active for the 71-d tracking period, moving through depths and temperatures ranging from the surface to 320 m and 5·8 to 21·0°C, respectively. The shark displayed temporal variation in its residence depth and exhibited a marked temperature preference, with 72% of the temperature observations between 15·0 and 17·5°C. This track provides evidence that the basking shark associates with the continental shelf and shelf edge off the south-eastern United States during autumn. Moreover, it corroborates previous studies indicating that the basking shark remains active and does not hibernate during autumn.

The distribution and ecology of subspp. anceps and edentatus of F. distichus L. emend. Powell (1957) in Britain and Ireland is described in detail, based on recent ecological surveys and critical examination of all past records.

F. distichus anceps is a small form confined to certain very exposed coasts in the north and west of Scotland and Ireland, where it reaches the southern limit of its geographical range. This plant may be a relict form in Britain, existing now only under an extraordinarily narrow range of rigorous habitat conditions; it is not thought to be actively extending its range southwards at the present time. The ecology of subsp. anceps is considered principally in relation to that of other reduced fucoids found on exposed British shores, viz. F. spiralis f. nana and F. vesiculosus f. linearis; all three forms are illustrated by photographs and means of distinguishing them are described. The lifespan of subsp. ancepsis thought to be 2 to 3 years at some Irish sites, but may be longer at some of the Scottish sites.

Tube-dwelling diatoms are found in a variety of habitats, from marine to fresh water on different types of substrata; rock, wood, plant and animal. I have described species as tube-dwelling (Cox, 1975 b) if they produce mucilage which is consolidated into a tubular structure around the cells, yet within the mucilage tube individual cells move and divide. The tube is usually attached to the substratum at its base and is extended apically by the secretion of more mucilage by the enclosed diatoms. Tube volume thus increases to accommodate the increased endotubular diatom population. The presence of tube-dwelling diatoms on rocky shores has been recorded by some workers (Aleem, 1949, 1950; Castenholz, 1963, 1967; Hopkins, 1964), while Castenholz (1963, 1967) correlated seasonal and distribution patterns of some littoral species with their response to light intensity and day-length. Carter (1932,1933) described the algal flora, including several tube-dwelling species, of two salt marshes but little work has been done on tube-dwelling diatoms occurring in estuaries. During the course of a study on the biology of these diatoms (Cox, 1975 ft) variation in their distribution at two Severn Estuary sites prompted an investigation into their distribution in the estuary as a whole. Diatom distribution was recorded with reference to the geographical location in the estuary and to the position on the shore at two sites lower down the estuary (Clevedon and Weston-Super-Mare).

The brittle-star Ophiothrix fragilis forms dense aggregations on the sea bed off Plymouth, as well as in other parts of the English Channel. From about 1970 there was a marked decline in populations off Plymouth, and study of previous records suggests that there have from time to time been considerable fluctuations in abundance of this species — since beds were first reported by E. J. Allen in the 1890s. The decline did not extend to populations in the southern and eastern parts of the Channel. The distribution of Ophiocomina nigra, which sometimes occurs in mixed populations with Ophiothrix, is also described. This species is more or less limited to the western Channel, and populations, which are nowhere very dense, showed no decline comparable to that of Ophiothrix.

Predation by the starfish Luidia ciliaris and L. sarsi is thought to be a likely cause of the disappearance of Ophiothrix. Luidia spp. are active predators on ophiuroids and other echinoderms, and numbers of L. ciliaris were observed in the vicinity of the Ophiothrix beds at the time of the decline. Both species of Luidia have a ’western’ distribution in the Channel, and showed an increase in density off Plymouth after the late 1960s, which is probably related to a changeover from a Sagitta setosa to a 5. elegans plankton community from 1968 on. The distribution of these Luidia is confined to stratified waters in the western Channel, surviving stocks of Ophiothrix being limited to mixed waters in the southern and eastern Channel where Luidia does not occur.

The occurrence of genetic differentiation among western Mediterranean Hediste diversicolor (Polychaeta: Nereididae) populations was assessed by allozyme electrophoresis on cellulose acetate. Seventeen loci were analysed in four populations. The level of the genetic variability was markedly low (mean HL range: 0.014–0.034), but comparable to that of other brackish water nereidids. The values of Nei genetic distance index (D) confirm the existence of genetic differentiation between the geographically isolated populations at Venice, Elba, Navicelli and Serchio D range: 0.128–0.356). However, the two samples from Serchio and Navicelli, ~15 km apart, were not genetically different (D=0·00005). The level of genetic differentiation in H. diversicolor populations followed the isolation-by-distance model. Reduced gene flow among H. diversicolor populations may be explained by its limited dispersal capacity and the eco-physiological barriers that occur between different brackish habitats.

Samples of Ostrea edulis were collected during 1999 and 2000 from five sites in Scotland, and from one site each in Northern Ireland, Ireland, France, The Netherlands and Norway. Samples were scored at four microsatellite loci. Mean numbers of alleles per locus varied from 12·6 to 16·6 and observed heterozygosity per locus ranged from 0·801 to 0·845. Samples derived originally from hatchery seed showed significantly fewer alleles per locus and significantly reduced expected heterozygosity compared with wild populations. However, observed heterozygosity did not differ significantly between the two groups. Significant deficiencies of heterozygotes were present at one or more loci in four of the ten populations sampled and a significant excess of heterozygotes was present at one locus in a hatchery-sourced Scottish population. Genetic distance indices revealed that the Norway population was the most distinct from all others and that hatchery-sourced populations were also relatively distinct from other wild populations. However, genetic subdivision was generally low implying high historical ‘migration’ rates for these populations.