Fine structure of some prosobranch ospharadia

The fine structure of the osphradia of Buccinum undatum 1. three Hawaiian Conus spp., Nassarius reticulatus (L), Nucella lapillus (L) and Littorina littorea (L) was examined. There is a remarkable uniformity in the arrangement of ultrastructural cell types in all the ospharadia investigated. The marginal glandular region is characterised by a single layer of cells, bearing a regular pallisade of microvilli and including two types of mucous cell. The epithelium of the sensory region is several cells deep, and bears a complex layer of microvilli in many orientations. Besides indifferent cells it contains two types of cell bodies of ciliated nerve processes. One type ends at the surface of the sensory region. The other, containing an elaborate array of smooth membranes in the perikaryon, has a process which enters the transitional region between sensory and glandular areas. In the transitional region, specialised cells with motile cilia adjoin the glandular region, and similar, but unciliated cells, containing large pigment granules scattered throughout the cytoplasm, adjoin the sensory region. The distal surface of both cell types is dissected by elefts extending 2 to 3 proximally, then widening into extensive spaces which contain cytoplasmic processes. The ciliated neurites which enter the transitional region end in the spaces at the base of the unciliated transitional cell elefts. It is suggested that the neuroepithelial cell processes, both those distributed over the sensory region and those concentrated in the transitional region, are receptors.     

Feinstruktur des Riechepithels von Chimaera monstrosa (Holocephali)

The epithelia of the olfactory folds of Chimaera monstrosa L. were studied by electron microscope. The greater part of each fold — including the secondary ones — is covered by sensory epithelium, whereas mere ciliary epithelium occurs on the tips of the folds. The olfactory epithelium is composed of ciliary cells, receptor cells, a few supporting cells, and basal cells. Mucous cells are restricted to the ciliary epithelium. As the apical region of the ciliary cells contains numerous vacuoles, including probably mucous substances, they may serve as producers of the superficial olfactory mucous layer. The ciliary basal bodies have two types of rootlets, the structure of which is described. Two morphologically different olfactory receptor cells could be identified: (1) receptors with a single, rod-shaped, free appendage (length 1.5 to 2 μm, diameter 0.1 to 0.5 μm), containing neurotubules, fibril bundles, and vesicles; (2) receptors whose dendrite bears few microvilli (length 2 to 3 μm, diameter 0.06 to 0.08 μm) projecting from a small vesicula olfactoria. Ciliary receptors are absent. The olfactory epithelium also contains sparsely distributed “brush” cells and a very few “giant” cells. Each “brush” cell bears a cluster of up to 250 microvilli (length 5 to 6 μm, diameter 0.1 μm) with 1 or more central tubulus and fibrils, the latter running into the cell body. The apical region of a brush cell contains densely packed mitochondria, which may indicate high metabolic activity; the function of this cell is unknown. The “giant” cell extends from the basal lamella to the epithelial surface. The ultrastructure of this cell does not reveal its special function.     

Growth response of Chaetoceros calcitrans (Bacillariophyceae) in batch culture to a range of initial silica concentrations

Batch cultures of the marine unicellular centric diatom Chaetoceros calcitrans (Paulsen) Takano were maintained by serial subculturing every 4 d into nutrient-enriched natural sea-water medium supplemented with 350, 950 and 1 400 g-at Si l^-1. The diatom cultures removed initial silica concentrations of 350 and 950 g-at l^-1 from the medium within 2 and 3 d, respectively. About 30 g-at l^-1 of the highest initial concentration remained in the medium after 4 d. The mean final cell density with an enrichment of 350 g-at Si l^-1 was 3.43±0.26×10⁴ cells l^-1 (median cell volume = 77.5±5.0 m³); with 950 g-at Si l^-1, 8.55±0.55×10⁴ cells l^-1 (50.0±4.5 m³); and with 1 400 g-at Si l^-1, 9.72±0.48×10⁴ cells l^-1 (37.3±5.0 m³). There was no significant difference in the final total organic weight of cells produced, which was in the range of 170 to 190 mg per 250 ml culture. This consisted of proportionately more lipid and carbohydrate and less protein from the treatment with 350 g-at Si l^-1 than from the 1 400 g-at Si l^-1 treatment.     

Effect of zinc on growth and development of larvae of the Pacific oyster Crassostrea gigas

Following the observation of periodic high concentrations of zinc in estuarine waters used in the White Fish Authority's oyster hatchery at Conway, North Wales, two beaker trials were conducted to study the effect of zinc, over the range recorded, on the young stages of larvae of Crassostrea gigas. Zinc, added to sea water both as zinc sulphate and as a natural mine-adit water, was applied for a period of 5 days, after which larvae were maintained for a further 5 days in sea water alone. Increasing concentrations over the range 125 to 500 g/l Zn resulted in decreasing growth, and increasing incidence of abnormality and larval mortality. A second trial with zinc sulphate showed 50 g/l Zn to have little effect on larval development, a progressive decrease in growth at 100 and 150 g/l, and no growth at 200 g/l. It is suggested that the deleterious effect of short-term exposure to zinc may well have contributed to the intermittent failure of larvae and irregular productivity previously recorded at the hatchery. It is also possible that zinc contamination in estuaries may affect natural oyster breeding, and may have to be considered in the future siting of hatcheries for seed production.     

Sublethal effects of zinc and municipal effluents on larvae of the red abalone Haliotis rufescens

Experiments were conducted to develop a sensitive sublethal toxicity test protocol to determine the toxicity of municipal wastewater effluents to larvae of the red abalone Haliotis rufescens. In multiple tests, fertilized abalone embryos were exposed for 48 h to dilutions of a reference toxicant, zinc sulfate, and to dilutions of primary-and secondary-treated effluents. The resulting veliger larvae were examined microscopically for larval shell abnormalities. In a longer flowthrough experiment, abalone were exposed for the entire larval phase, from the two-cell stage through metamorphosis, to compare zinc effects on metamorphosis with zinc effects on short-term larval shell development. Dissolved oxygen, pH, salinity and temperature were measured daily in test solutions, and zinc concentrations were verified by chemical analysis. No observed effect concentrations (NOECs) for zinc were 39±2.1 g l^-1 in three 48 h exposures, and 19 g l^-1 for the 9 d exposure through metamorphosis. Median effect concentrations (EC₅₀s) were 68±6.9 g l^-1 in 48 h tests and 50 g l^-1 in the 9 d test. Abalone larvae were affected at lower concentrations of primary than of secondary effluent.     

Effects of cadmium and low magnesium on cell division and calcification in the marine coccolithophorid Cricosphaera (Hymenomonas) carterae

Cadmium (Cd) added to normal media and to magnesium (Mg)-deficient media produced inhibitory effects on cell division and cell calcification in the marine coccolithophorid alga Cricosphaera (Hymenomonas) carterae. Compared with controls in normal media (with 25 mM Mg), cell growth decreased progressively with Cd at concentrations of 5–20 M. In Mg-deficient media (with 6 mM and 0.08 mM Mg) the inhibitory effects were more pronounced with complete arrest of cell division at 20 M Cd. The greatest Cd inhibition occurred in media with the lowest Mg concentration (0.08 mM). Cadmium (5–40 M) also decreased recalcification (coccolith formation) in cells previoasly decalcified with CO₂ with complete inhibition at 40 M Cd. Inhibition of recalcification in various Cd concentrations (5–40 M) was more pronounced in low-Mg medium (with 6 mM and 0.08 mM Mg) compared with normal medium (25 mM Mg). Partial or complete reversal of the inhibitory effects of Cd and low Mg media on cell division and calcification occurred following a wash and resuspension of the cells in normal control medium (25 mM Mg).     

Selective particle ingestion by oyster larvae (Crassostrea virginica) feeding on natural seston and cultured algae

I investigated selective particle ingestion by oyster larvae (Crassostrea virginica) feeding on natural seston from Chesapeake Bay and laboratory-cultured algae of different sizes or chemical content. In 15 of 16 experiments with complex natural suspensions as food, small(<150 m) and large (>150 m) larvae selected most strongly for small (2 to 4 m) food particles, but in the presence of a large (>10 m)-cell dinoflagellate bloom, large larvae strongly selected much larger (22 to 30 m) food material (presumably dinoflagellates). When fed simplified mixtures of four cultured algal species (Synechococcus bacillaris, Isochrysis sp., Dunaliella tertiolecta, and Prorocentrum minimum) ranging in size from 1 to 11 m, small larvae preferred 1 m algae while large larvae preferred 11 m algae. In experiments with algal mixtures, and with suspensions of natural particles and added algae, large larvae preferred algal species harvested from exponential-phase cultures over other species from stationary-phase cultures. Larval ingestion rates of the cultured alga Thalassiosira pseudonana were about three times higher for cells with a low carbon:nitrogen ratio (7.2:1) than for high C:N ratio (16.2:1) cells when these cells were offered separately in suspensions of equal concentration. As a result, more algal cells, algal C, and algal N was ingested by larvae fed low C:N cells. However, larvae did not show a significant preference for either type of cell when they were offered in a 1:1 cell mixture. Feeding patterns of C. virginica larvae in natural food suspensions can vary with the composition of these complex suspensions, and ingestion seems dependent not only on the size, but on the growth rate and chemical quality of food particles.     

Nutrition studies in the nauplius larva of Calanus pacificus (Copepoda: Calanoida)

Nauplii of Calanus pacificus were raised on a mixture of algae. Details of the mouth-parts, such as denticles, labial palps and lobes, setations and structure of the masticatory teeth were examined by scanning electron microscopy (SEM). Under the experimental conditions (15°C and 300 gC l^-1), exponential growth coefficients for the period Nauplii II–VI were 0.179 for carbon and 0.228 for nitrogen. C:N ratios dropping from 5.1 to 4.7. Growth was isochronous, each stage lasting 1.5 days. Respiratory losses were 15 to 19.6% of body carbon daily. Nauplii raised on a given alga showed higher rates of ingestion in the presence of this food, compared to nauplii switched to other algae. Minimal threshold concentrations for feeding were found, depending on the size of the food offered and ranging from 5.8 gC I^-1 for Lauderia borealis (28.7 m spherical diameter) to 47.1 gC 1^-1 for Chlamydomonas sp. (11.0 m). Unlike the Copepodite I stage, Nauplii II–VI larvae were not able to ingest small cells such as Isochrysis galbana (4.3 m), or very large ones such as Ditylum brightwellii (47.5 m) at more than maintenance rations. Below the critical concentration for maximal feeding, ingestion was clearly dependent on size of the cells offered, but the size-dependent relationship was different for diatoms and non-diatoms. Filtering rates increased from a threshold concentration to a maximal rate at about 50 gC 1^-1, and decreased at higher concentrations. Critical concentrations ranged from 125 gC 1^-1 for L. borealis to 1000 gC 1^-1 for Chlamydomonas sp. Maximal daily rations ranged between 100 and 150% of body carbon.     

Larval development in the Antarctic nemertean Parborlasia corrugatus (Heteronemertea: Lineidae)

Embryonic and larval development were followed from fertilisation to settlement in the Antarctic heteronemertean Parborlasia corrugatus (McIntosh, 1876). The first cleavage occurred 10 to 15 h after fertilisation, and the second at 17 h. Larvae hatched at the gastrula stage, between 170 and 200 h post-fertilisation, and were 150 m in diameter. Early larval stages aggregated in dense groups near the surface of incubation vessels and were positively phototactic. Early pilidium larvae were recognisable 435 h post-fertilisation. They were 155×152 m in size, and possessed a complete apical tuft of cilia and a full marginal band of locomotory cilia. At this stage, the gust was visible through the body wall, and the mouth was open and was 40 m in diameter. Late pilidia, 222×193 m in size, were helmet-shaped. They had an apical tuft over 100 m long, and possessed a lobed marginal band of locomotory cilia. Pilidia were observed aggregating close to the bottom of incubation vessels 1200 to 1350 h (50 to 56 d) after fertilisation, and this was interpreted as settlement behaviour. At this stage, the apical tuft had been lost and they were highly contractile, being capable of compressing their bodies. However, neither developing juveniles within the larval envelope nor hatched juveniles were observed. Pilidia consumed the microalgae Tetraselmis suecica, Thalassiosira pseudonana and Isochrysis galbana. They also fed on particulate organic material < 1 m in size, as shown by the presence of material in the guts of larvae offered filtered extracts of algal cultures. There was some indication that larvae could use dissolved organic material, since pilidia held in seawater with organic material removed did not survive as long as those in filtered seawater or in filtered water with added amino acids. However, the only larvae to exhibit settlement behaviour in the feeding experiments were those offered Tetraselmis succica and Thalassiosira pseudonana, and these required a longer development time to reach this stage than pilidia in the standard cultures, where a mixed algal diet was offered.     

Intracellular localization of vanadium in the fan worm Pseudopotamilla occelata

A very high level of vanadium was found to be contained in the polychaete worm Pseudopotamilla occelata collected in 1992–1993 from the Sanriku coast on the main island of Japan. The vanadium concentration (mean±SD=5500±1800 g g^-1 dry wt) in the worm's branchial crown which is composed of many bipinnate radioles was approximately 100 times higher than that (mean±SD=60±25 g g^-1 dry wt) in the trunk body. Electron probe X-ray microanalysis revealed that a large amount of vanadium was present in the outer potion of the epidermis of the bipinnate radiole. Analytical electron microscopy for a cryo-section of the bipinnate radioles indicated that vanadium was localized in electron-dense deposits in the apical portion of epidermal cells. From an examination of the fine structures, the locality of the electron-dense deposits were found to correspond to that of the apical vacuoles in the epidermal cells. It was concluded that most of the vanadium in P. occelata was contained in the vacuoles of the epidermal cells of the bipinnate radioles.     

Simplified method for the determination of acid-soluble sulfides in marine sediments

A simple, rapid method for the measurement of acid-soluble sulfides from marine sediments, in the range of 0 to 350 g sulfide, was developed. Using the mean of 4 replicates, the maximum sensitivity of the method is ±5.48 g. The method is based on iodometric back titration after the reaction of a standard iodine solution with the sulfide, which is precipitated on paper wicks as zinc, sulfide. The mean coefficient of variation, based on raw titration data, is 0.71% for aliquots from field samples, 0.41% for standards, and 0.21% for blanks. The method is used to compare zinc acetate-fixed subsamples, one group having been stored for 1 month in a refrigerator at 5°C and the other having been analyzed immediately after collection. No significant differences in sulfide content between subsamples, at the 95% confidence level, were noted.     

A unique low molecular weight zinc-binding ligand in the kidney cytosol of the musselMytilus edulis,and its relationship to the inherent variability of zinc accumulation in this organism

Mussels,Mytilus edulis, are known to have a high degree of variability in their whole soft tissue zinc concentrations which cannot be explained by any known ecological or physiological factor. In the present study, 70 individual mussels collected from an uncontaminated site at Bellevue, Newfoundland, in Spring 1987 had kidney zinc concentrations ranging from 148 to 4 907 g g^-1 dry weight while 40 mussel exposed to 25 g l^-1 zinc for 18 d had kidney zinc concentrations ranging from 144 to 14 072 g g^-1. Pooled or individual kidneys were homogenized in 50 mM ammonium bicarbonate buffer (pH 8.0) and ultracentrifuged for 1 h at 105 000 g. On average, about 70% of the total kidney zinc load was found in the 105 000 g pellet. Cytosolic zinc was separated into two peaks on a column of Sephadex G-25. The first peak coincided with the void volume of the column representing molecules with molecular weights of at least 5 000 (exclusion limits of Sephadex G-25). This peak would include any metallothionein present since mussel metallothionein has a molecular weight of 10 000 to 20 000. Little variability was observed in this peak so it was concluded that zinc-thionein did not play a major role in the genesis of the inherent variability. The second peak represented zinc complexed to an unknown substance with an approximate molecular weight of 700 to 1 300. This very low molecular weight zinc showed an extremely high degree of inherent variability and a strong positive correlation with the whole kidney zinc concentration. It is concluded that this very low molecular weight zinc complex plays a major role with regard to kidney zinc variability. Some very low molecular weight zinc was also noted in the digestive gland and gills. It is speculated that this substance may aid in zinc transport as well as in the incorporation of zinc into granules.MSRL Contribution No. 720     

Production and role of hyaline hairs in Ceramium rubrum

Light intensity within the range of 40 to 210 E · m^-2 · s^-1 had relatively little effect on the abundance, length or distribution of Ceramium rubrum unicellular, hyaline hairs. External NH ₄ ⁺ concentrations less than 0.5 M stimulated hair initiation and growth in apical regions of the thalli. Ammonium concentrations in excess of 20 M inhibited hair formation on all regions of the thalli. Ammonium uptake velocities of plants with hairs were approximately twice those of plants without hairs. These hairs may be adaptive to take advantage of intermittent bursts of nutrients by increasing the plant's surface area and, hence, the number of nutrient uptake sites.Woods Hole Oceanographic Institution Contribution No. 5526     

Relationship between phytoplankton cell size and the rate of orthophosphate uptake: in situ observations of an estuarine population

Orthophosphate uptake by a natural estuarine phytoplankton population was estimated using two methods: (1) ³²P uptake experiments in which filters of different pore sizes were used to separate plankton size-fractions; (2) ³³P autoradiography of phytoplankton cells. Results of the first method showed that plankton cells larger than 5 m were responsible for 2% of the total orthophosphate uptake rate. 98% of the total uptake rate occurred in plankton composed mostly of bacteria, which passed the 5 m screen and were retained by the 0.45 m pore-size filter. There was no orthophosphate absorption by particulates in a biologically inhibited control containing iodoacetic acid. Orthophosphate uptake rates of individual phytoplankton species were obtained using ³³P autoradiography. The sum of these individual rates was very close to the estimated rate of uptake by particulates larger than 5 m in the ³²P labelling experiment. Generally, smaller cells were found to have a faster uptake rate per m³ biomass than larger cells. Although the nannoplankton constituted only about 21% of the total algal biomass, the rate of phosphate uptake by the nannoplankton was 75% of the total phytoplankton uptake rate. Results of the plankton autoradiography showed that the phosphate uptake rate per unit biomass is a power function of the surface: volume ratio of a cell; the relationship is expressed by the equation Y=2x10^-11 X ^1.7, where Y is gP m^-3 h^-1 and X is the surface: volume ratio. These results lend support to the hypothesis that smaller cells have a competitive advantage by having faster nutrient uptake rates.     

Chemotactic effects of nutrients on spores of the kelps Macrocytis pyrifera and Pterygophora california

Fertile Macrocystis pyrifera (L.) C. Ag. and Pterygophora californica Rupr. were collected in California, USA in 1987 to 1988. Spores of the kelps exhibited both positive and negative chemotaxis to a variety of chemical nutrients. Chemotaxis was measured by counting the number of spores that swam into flattened capillary tubes with the chemical relative to the number that swam into control tubes. Video-motion-analysis also showed that P. californica spores swam towards a nitrogen source more often than they swam away. Similar chemotactic effects were observed in both 2 and 8 h-old preparations. M. pyrifera spores swam towards nitrate, ammonium (1 to 90 M), glycine, aspartate iron (1 m), boron, cobalt, and manganese. Negative chemotaxis was elicited by ammonium (1 000 M) and iron (45 M). Neither phosphate nor zinc had significant effects. P. californica spores were attracted by nitrate, ammonium, phosphate, and boron. Negative chemotactic effects were recorded with iron (45 M) and manganese. Iron (1 M), cobalt, and zinc had no effect. It is suggested that chemotactic behavior is an adaptation which allows the kelp spores to find and settle in microhabitats suitable for gamatophytic growth and reproduction.     

Functional morphology and significance of the circulatory system of Ostracoda,exemplified by Vargula hilgendorfii (Myodocopida)

Combined high-resolution video-recordings of live specimens, SEM and serial microtome sections were used to document the morphofunctional aspects of blood (hemolymph) circulation in Ostracoda, exemplified by the nektobenthic myodocopid Vargula hilgendorfii from Japan. The circulatory system is comprised of a single-chambered dorsal heart (pericardium, myocardium with two ostia), efferent vessels (aorta and secondary arteries) and an integumental afferent network of sinuses radiating from the adductor muscle area to a peripheral channel leading to heart. The heartbeat and the linear velocity of hemolymph in sinuses range from 0.5 to 6 times s^-1 and 200 to 1000 m s^-1, respectively. Hemocytes (10 to 17 m) of irregular shapes occur within the circulating hemolymph. This typical open circulatory system is found in most myodocope ostracodes and other crustaceans. It is totally absent in small (mostly <2 mm) ostracodes such as Podocopa. We conclude that the fluid convection of hemolymph augments the diffusion process of O₂ in larger animals. Oxygen uptake is assumed to occur preferentially through the inner (posterior) surface of the carapace where hemolymph sinuses are best developed and in close contact with sea water. Hemocytes may be involved in coagulation processes as in other crustaceans (e.g. Decapoda). Integumental circulation, preserved as anastomosing features in fossil Ostracoda, is known from the early Palaeozoic through to the Recent.     

Photoinhibition at low quantum flux densities in a marine dinoflagellate (Amphidinium carterae)

Growth and photosynthetic properties of the marine dinoflagellate Amphidinium carterae Hulbert were examined under continuous illumination in batch cultures at four different irradiances between 2 and 150 E m^-2 s^-1. The slope of both cell- and Chl a-based photosynthesis versus the irradiance curves was greatest for cells grown at 15 E m^-2 s^-1. The relative Chl a values cell^-1 were 1, 1.5 and 2 for cultures grown at 150, 80 and 15 E m^-2 s^-1, respectively. A low-temperature (-196°C) fluorescence technique was used to examine cells for photoinhibiton. Photoinhibition was greatest for cells grown at 150 E m^-2 s^-1. However, significant photoinhibition of this species was noted even at 80 E m^-2 s^-1. No significant difference in the fluorescence pattern was found between cells grown at 2 and 15 E m^-2 s^-1. Time course studies indicate that photoinhibition may occur within 2 h following exposure to 350 E m^-2 s^-1 in cells grown at 15 E m^-2 s^-1 and is reversible when light levels are lowered within 4 h. The ecological significance of phytoplankton unable to cope with excess photosynthetic excitation energy is discussed.     

Effect of heavy metals (Zn,Hg, Cu,Cd, Pb,Ni) on the length growth of Mytilus edulis

The shortterm (10–22 d) effect of Zn, Hg, Cu, Cd, Pb, and Ni on the length growth of Mytilus edulis is studied. Significant reductions of growth rate was found at 0.3 g Hgl^-1, 3 g Cul^-1, 10 g Znl^-1, and 10 g Cdl^-1 added to the local sea water, while concentrations of up to 200 gl^-1 of Pb and Ni had no effect on the growth. With exposure to Cu and Zn, there was a linear reduction in growth rate with increasing metal concentration up to about 6 g Cul^-1 and 100 g Znl^-1. Above these levels, growth stopped with Cu, while with Zn it was stabilized at about 20% of control growth. When Hg and Cd were added, a curvilinear relationship between growth and metal concentration is indicated. With Hg, growth rate is nearly zero above 3–4 g Hgl^-1, while the growth rate was 50% of control after 10 d of exposure to 100 g Cdl^-1. At 2 g Cdl^-1 there was a significant stimulation of length increase. Observed EC₅₀-values for growth were 0.3–0.4 g Hgl^-1, 3–4 g Cul^-1, 60 g Znl^-1, and 100 g Cdl^-1.     

Mytilus edulis planulatus: an “integrator” of cadmium pollution?

Mussels, Mytilus edulis planulatus, were collected from Port Phillip Bay, Victoria, Australia, in February 1984, to test the assumption that they are integrators of cadmium pollution. Groups of mussels were subjected to the same average dose of cadmium (21 g l^-1), administered according to different dosing regimes over 4 wk (Regimes 1, 2, 3, 5); other groups received twice the average dose (42 g l^-1) in half the time (Regime 4). During each regime, the mussels were exposed to the different cadmium concentrations for one week at each concentration. Nominally, the regimes were: (1) 36 g (Wk 1) to 26 g (Wk 2) to 16 g (Wk 3) to 6 g (Wk 4) Cd l^-1; (2) 6 to 16 to 26 to 36 g Cd l^-1; (3) 21 to 21 to 21 to 21 g Cd l^-1; (4) 42 to 42 g Cd l^-1; (5) 42 to 42 g Cd l^-1 to background (<0.5 g) to background. Differences in cadmium accumulation by mussels from Regimes 1 and 4 were not statistically significant, nor were differences in accumulation between mussels from Regimes 2 and 3. However, mussels from Regimes 1 and 4 had accumulated significantly more cadmium than had mussels from Regimes 2 and 3. Accumulation by mussels from Regime 5 was not significantly different from that by mussels from any of the other regimes. These results suggest that, at least for cadmium, the assumption that mussels are integrators of pollution should be treated with caution. They also have implications with regard to the quantitative biological monitoring of pollution. For example, even in a carefully controlled monitoring program, using mussels of standard size and condition, significant differences in cadmium content between mussels need not indicate exposure to different levels of contamination. Rather, these differences could reflect differences in the regime by which the contamination was received.     

Size composition of particulate organic matter in the lagoon of Tikehau atoll (Tuamotu archipelago)

Suspended particulate matter was comprehensively investigated from 6 to 17 April 1986 in the lagoon of Tikehau atoll (15°00S; 148°10W). Dry weight (DW), particulate organic carbon (POC), adenosine triphosphate (ATP), and chlorophyll a were measured for five size-classes (0.2 to 0.8 m, 0.8 to 3 m, 3 to 35 m, 35 to 200 m, and 200 to 2000 m). Taxa were identified and counted for the whole plankton (both autotrophic and heterotrophic). Particles <3 m accounted for 81% of the total POC (192 mg m^-3), and detritus comprised 82% of the total POM. Phytoplankton (cyanobacteria plus algae) accounted for 35% of the living carbon, 75% of which consisted of heterotrophic bacteria and cyanobacteria. The zooplankton biomass was composed of 31% nano-, 26% micro-, and 43% mesoplankton.