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.     

Autoradiographic study to detect metabolically active phytoplankton and bacteria in the Rhode river estuary

The rate of utilization of inorganic carbon (C) and phosphate (P) by phytoplankton and bacteria in the Rhode River estuary has been estimated using liquid-emulsion autoradiography during four times of the year. Metabolic activity of phytoplankton was estimated by calculating silver grains above individual species. From these counts, the relative C and P uptake rates of individual species per unit of biomass and per volume of water were estimated. Examination of the autoradiograms showed that the metabolically most active, algae were smaller than 10 m. Both C and P were paken up by these smaller species at a higher rate than their proportion of the total biomass per volume of water would indicate. Uptake of C and P per unit of cell volume varied within a species and among the various phytoplankton at the different seasons of the year. Metabolic activity of planktonic bacteria in safranin-stained autoradiograms was also estimated by counting bacteria with associated grains and cells without grains. The ratio of 33p-labeled to unlabeled bacteria was highest in November. This high metabolic activity of bacteria in November corresponded with high P uptake rates of the phytoplankton at that time. Throughout this study, only 28 to 42% of the total phytoplankton biomass was metabolically active and, 63 to 85% of the bacteria.     

Seasonal changes of benthic bacteria in a seagrass bed (Posidonia oceanica) of the Ligurian Sea in relation to origin,composition and fate of the sediment organic matter

Variations in number and biomass of benthic bacteria were examined in the surface sediments of a Mediterranean seagrass bed [Posidonia oceanica (L.) Delile] in the Gulf of Marconi (northwestern Mediterranean Sea) from 1990 to 1991. The annual dynamics of benthic bacterial density and biomass were compared to changes in elemental (organic C and total N) and biochemical (lipids, proteins, carbohydrates) composition of sediment organic matter, as well as to microphytobenthic biomass, dissolved inorganic nutrients and ATP. Bacterial densities exhibited marked seasonal variations (5.12 to 322.7x10⁸ cells g^-1 sediment dry wt) with highest values in late spring. Bacterial standing stocks (15.8 to 882.33 g C g^-1 of sediment dry wt) were high. Bacterial biomass did not correlate with organic C, total N or to specific biochemical components, but correlated significantly with chlorophyll a, ATP and porewater phosphate concentrations. There is evidence that benthic bacteria were responding to variations of algal biomass. Bacterial biomass accounted, on average, for 30% of total living carbon (calculated on the basis of the ATP concentrations) and 8.4% of total organic carbon.     

Some experiments on phosphate assimilation by coastal marine plankton

A study of phosphate assimilation by coastal marine plankton revealed that both phytoplankton and microheterotrophs incorporated radioactive phosphorus (³³P). Size fractionation of the particulate matter (using 1 m pore diameter Nucleopore^® membrane filters), antibiotic treatment (using garamycin), and independent estimaties of photoautotrophic (¹⁴CO₂ uptake) and heterotrophic (³H-glucose uptake) activities were employed to separate phyto- and bacterioplankton phosphate uptake. Results indicated that phytoplankton ³³P-uptake was best estimated by the fraction of particulate matter retained on the 1 m membrane filters. Usually, less than 10% of the phytoplankton (based on chlorophyll a measurements) passed the 1 m pore-diameter filters, whereas about 90% of the heterotrophic activity passed. At least 50% of the ³³P-uptake was associated with the <1 m fraction. It may be possible to resolve the phytoplankton and bacterial contributions to ³³P-uptake by comparing the percent of total ³³P-uptake with the percent of total ³H-glucose uptake associated with the >1 m fraction.     

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.     

Pathway and products of CO2-fixation by green prokaryotic algae in the cloacal cavity of Diplosoma virens

Light-dependent ¹⁴CO₂ fixation by the algae of Diplosoma virens (Hartmeyer) ranged between about 3 and 27 moles mg^-1 chlorophyll h^-1. The principal first products of ¹⁴C fixation were 3-phosphoglyceric acid and phosphorylated sugars, indicating that ribulose bisphosphate carboxylase was the primary carboxylation enzyme. The activity of this enzyme in crude extracts of the algae was 4 to 6 moles CO₂ mg^-1 chlorophyll h^-1. The principal end product of ¹⁴C fixation by these algae in the ascidian host was a water-soluble oligosaccharide which was an -1,4-glucan. A maximum of 7% of the ¹⁴C fixed was found in insoluble materials of the algae or its host after 60 min ¹⁴CO₂ fixation. Whether the -1,4-glucan is a product of algal or animal metabolism remains to be determined.     

Phosphorus metabolism of oceanic dinoflagellates: phosphate uptake,chemical composition and growth of Pyrocystis noctiluca

The phosphorus metabolism of Pyrocystis noctiluca Murray (Schuett) 1886 has characteristics which may enhance its potential for success in orthophosphate impoverished waters. The steady-state phosphate uptake rates were equal in the light and dark, and were directly proportional to both the phosphorus cell quota and the cell division rate. In contrast, nutrient-saturated uptake rates were multiphasic, faster in the light than the dark, 2 to 4 orders of magnitude greater than steady-state rates, and were inversely proportional to both the phosphorus cell quota and the cell division rate. These uptake characteristics suggest that P. noctiluca may take up phosphate coincidently at their typically low ambient concentrations as well as to exploit episodic nutrient events in nature. Cell division rates were a hyperbolic function of the ambient orthophosphate concentration. The shortest doubling time was 8.7 d, the phosphate concentration at half the maximum division rate was 0.15 M and the threshold, concentration for cell division was ca 0.05 M PO ₄ ^3- . Division rates of P. noctiluca in the ocean are much faster than predicted from the measured ambient orthophosphate concentrations. Since this dinoflagellate has high naturally occurring alkaline phosphatase activities, and can utilize organic-P compounds, we suggest that organic-P can be as important as orthophosphate in supporting the observed division rates of P. noctiluca in the sea.     

Juvenile growth of the polychaete Nereis virens feeding on a range of marine vascular and macroalgal plant sources

A laboratory experiment was conducted to examine variation of juvenile growth (% d^-1) of the polychaete Nereis virens (Sars) in relation to tidal flat plant species as food sources. We used vegetable materials (algae and vascular plants) which are carried along by tidal currents and are found abundantly at the upper tidal level. Juveniles (2-yr-old) markedly increased in wet weight with the algae Laminaria longicruris (weight-specific growth rate : 1.7% d^-1) and Enteromorpha intestinalis (: 1.6% d^-1) as food sources. A higher value of assimilation efficiency was observed for algal species (L. longicruris 55.1±7.9%; E. intestinalis 54.8±0.5%; Fucus vesiculosus 40.6%) than for marine vascular plants (Spartina alterniflora 26.8±10.9%; Zostera marina 1.4%). The digestion of marine vascular species lasts longer (19 to 38 h) than that of algal species. All these characteristics (growth, assimilation efficiency and duration of the digestive process) seem to correlate positively with lignin and cellulose concentrations in the plant structure.     

Distribution of lipopolysaccharide,an indicator of bacterial biomass,in subtropical areas of the sea

Lipopolysaccharide (LPS) concentrations, an indicator of bacterial biomass, were determined in the South China Sea and the Pacific Ocean. The distribution patterns of LPS were compared with those of chlorophyll a (Chl a), zooplankton biomass and the concentrations of several nutrients. LPS and total bacterial numbers in seawater were correlated with each other with a correlation coefficient (r) of 0.84 at Stations 7, 8 and 10. Diurnal fluctuation of LPS was negligible, but Chl a varied slightly in the vertical water column. Zooplankton stayed at a depth of around 400 m during the daytime and ascended quickly to the surface (0–50 m) early in the evening. The profiles of LPS and Chl a were negatively correlated to each other in the water layers above the Chl a maximum peak (r=-0.74; excluding the samples from 75 m at Station 7 and 10 m at Station 11 due to inadequate data for the statistical analysis). LPS and zooplankton biomass during the night-time, in contrast, paralleled each other at 5 stations surveyed (r=0.71). The presence of zooplankton resulted in an increase in bacterial numbers in the seawater in vitro. Based on these results, the factors controlling the occurrence and abundance of bacteria and phyto- and zooplankton in the pelagic sea are discussed.     

Untersuchungen über die heterotrophe Aktivität in der zentralen Ostsee

The distribution of some microbial parameters was studied at 3 stations in the Central Baltic Sea (Bornholm Basin, BB; Danzig Deep, DD; and Gotland Deep, GD) during May 1976. The following analyses were performed: total bacterial numbers and biomass, viable counts and maximum uptake velocity (V _max) of glucose. The values found for thesurface, samples were, total bacterial counts: 0.6x10⁶ (BB); 1.7x10⁶ (DD); 0.4x10⁶ (GD) cells/ml; bacterial biomass: 1.9 g C/l (BB); 6.9 g C/l (DD); 1.6 g C/l (GD); viable counts: 0.37x10³ (BB); 17x10³ (DD); 0.4x10³ (GD) counts/ml; V _max: 0.01 g glucose-C/l (BB), 0.06 g glucose-C/l (DD); 0.01 g glucose-C/l (GD). The relatively high microbial numbers and activities of the Danzig Deep may be associated with the fertilization of the area by the River Vistula. The vertical distribution of the microbial parameters in the Bornholm Basin and Danzig Deep showed high values both in the top layer (0 to 20 m) and in the deep layer (>40 m). In the intermediate layer, however, the values decreased significantly. It is suggested that the high values of the microbial parameters at depth are caused by at least two major processes during the inflow of North Sea water into the deep layers of the Baltic Sea: (1) the North Sea water may already have contained high numbers of bacteria; (2) during the inflow, the high concentrations of bacteria normally located at the sediment-water interface are distributed throughout the whole deep layer by mixing.

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Beitrag Nr. 143 aus dem Sonderforschungsbereich 95 Wechselwirkung Meer-Meeresboden, Universität Kiel.     

Anatomy of structures associated with air-breathing in Orchestia gammarellus (Crustacea: Amphipoda: Talitridae): coxal plates and gills

The structure of the coxal gills and coxal plates of the semi-terrestrial beachflea Orchestia gammarellus (Pallas) (Crustacea: Amphipoda: Talitridae) is described in relation to their possible use for aerial gas exchange and ion exchange. Anatomical evidence is presented to support the hypothesis that the medial surface of the coxal plates functions as an extrabranchial aerial gas-exchange site in O. gammarellus. Thus, the effective diffusion distance across the medial (or inside-facing) surface of O. gammarellus coxal plates (mean±SD=5.4±0.3 m; n=9, cuticle thickness 4.4±0.5 m, n=21) is only a third of the equivalent distance across both the coxal gills (18.4±6.0 m, n=10; cuticle thickness 1.7±0.6 m, n=7) and the lateral (or external) surface of the coxal plates (19.4±0.7 m, n=5; cuticle thickness 8.7±0.8 m, n=7). Chloride-ion-permeable areas were located using a silver-staining technique. All ten coxal gills appeared to be equally permeable to chloride ions after examination with a light microscope. However, the coxal plates and the rest of the integument do not appear to be chloride-permeable.     

Development of the pericalymma larva of Solemya reidi (Bivalvia: Cryptodonta: Solemyidae) as revealed by light and electron microscopy

Solemya reidi Bernard 1980 is a gutless protobranch bivalve known to possess intracellular chemoautotrophic bacterial symbionts in its gill. A light and electron microscope study on the embryology and larval development of S. reidi provides data for the bivalve Subclass Cryptodonta. S. reidi spontaneously spawned large eggs (271 m in diameter), which developed within individual gelatious egg capsules. The first several cleavages were equal and a distinct molluscan cross was formed at the animal pole of the embryo, features previously unreported in bivalve development. Lecithotrophic pericalymma larvae (similar to the larvae of paleotaxodont protobranch bivalves and aplacophoran molluscs) hatched at 18 to 24 h and remained in the water column for a further 5 d at 10°C. At hatching, larvae measured from 360 to 440 m in length and from 225 to 265 m in cross-sectional diameter. Definitive adult structures developed within an epithelial locomotory test entirely covered with compound cilia. The test histolysed at metamorphosis and was ingested throught the mouth into the perivisceral cavity. Length and height of the shell following metamorphosis was 433 m (±42 m, n=16) and 282 m (± 29 m, n=13), respectively. Primary data and data from the literature show that the type of larval development in both paleotaxodont and cryptodont bivalves cannot be reliably estimated from egg or prodissoconch sizes.     

Fractionated phytoplankton primary production,exudate release and bacterial production in a Baltic eutrophication gradient

The distribution of phytoplankton primary production into four size fractions (>10 m, 10-3 m, 3-0.2 m and <0.2 m), the utilization of algal exudates by bacteria and the bacterial production were studied in a eutrophication gradient in the northern Baltic proper. The polluted area exhibits substantially increased nutrient, especially nitrogen, levels while only minor differences occur in salinity and temperature regimes. Total primary production was 160 g C · m^-2 · yr^-1 at the control station and about 275 g C · m^-2 · yr^-1 at the eutrophicated stations. The estimated total exudate release was 16% of the totally fixed ¹⁴CO₂ in the control area and 12% in the eutrophicated area (including the estimated bacterial uptake of exudates). The difference in¹⁴CO₂ uptake rates between incubation of previously filtered water (<3, <2, <1 m) and unfiltered water was used to estimate bacterial uptake of phytoplankton exudates which were found to contribute about half of the estimated bacterial carbon requirement in both areas. Bacterial production was estimated by the frequency of dividing cells (FDC) method as being 38 g C · m^-2 · yr^-1 at the control station and 50 g C · m^-2 · yr^-1 at the eutrophicated stations. To estimate the mean in situ bacterial cell volume a correlation between FDC and cell volume was used. The increased annual primary production in the eutrophicated area was due mainly to higher production during spring and autumn, largely by phytoplankton cells (mainly diatoms) retained by a 10 m filter. Primary production duringsummer was similarin the two areas, as was the distribution on different size fractions. This could possibly explain the similar bacterial production in the trophic layers at all stations since the bulk of bacterial production occurs during summer. It was demonstrated that selective filtration does not quantitatively separate photoautotrophs and bacteria. A substantial fraction of the primary production occurs in the size fraction <3 m. The primary production encountered in the 3-0.2 m fraction was due to abundant picoplankton (0.5 to 8 · 10⁷ ind · l^-1), easily passing a 3 m filter. The picoplankton was estimated to constitute up to 25% of the total phytoplankton biomass in the control area and up to 10% in the eutrophicated area.     

Phosphate acquisition in the giant clam-zooxanthellae symbiosis

The effect of phosphate on the giant clam Tridacna gigas and on its symbiotic dinoflagellate Symbiodinium sp. was compared with that on cultured Symbiodinium sp. originally isolated from the same clarn species. Incubation of whole clams in elevated phosphate (10 M) reduced their capacity for phosphate uptake, but the uptake capacity of the clam's zooxanthellae population was not influenced. In addition, there was no change in the zooxanthellae density and the N:P ratio, of these algae., On the other hand, cultured zooxanthellae were influenced by the phosphate regimen of their culture medium. Compared with controls (0 M P), addition of 10 M phosphate to the culture medium caused an increase of 100% in cell density and decreases of 50% in the N:P ratio, and 80% in the phosphate-uptake capacity of the zooxanthellae. Zooxanthellae freshly isolated from the clams exhibited properties similar to those of zooxanthellae cultured in the absence of phosphate. These results demonstrate that the zooxanthellae population of T. gigas have limited access to the inorganic phosphate in sea water and the phosphate reserves within the animal host.     

Bacterivory of a mudflat nematode community under different environmental conditions

The fate of the benthic bacterial biomass is a topic of major importance in understanding how soft-bottom environments function. Because of their high abundance, production and nutritional value, benthic bacteria may constitute an important food resource for benthic fauna. The trophic role of bacteria for a nematode community on the Brouage mudflat (Marennes-Oléron-France), dominated by three species: Chromadora macrolaima (64% of the abundance), Daptonema oxycerca (15%) and Ptycholaimellus jacobi (8%), was determined in grazing experiments using ¹⁵N pre-enriched bacteria. On intertidal flats, seasonal, tidal and circadian cycles induce strong variations in environmental conditions. Grazing experiments were performed in order to measure the effects of abiotic (temperature, salinity and luminosity) and biotic (bacterial and algal abundances) factors on assimilation rates of bacteria by nematodes. In order to assess simultaneously bacteria and algal assimilation rates, algal abundances were modified adding ¹³C pre-enriched Navicula phyllepta. Assimilation rate was significantly lower at 5°C; moreover, general trend shows a prominent temperature effect with an optimum around 30°C. Assimilation at salinity 18 was not significantly different from the assimilation at salinity 31. Assimilation was higher under light conditions than in the dark. Above 10⁹ bacteria ml⁻¹, assimilation of bacteria remained unaffected by bacterial abundance. However, assimilation of algae increased with the algal concentration. Nematode kept feeding under conditions of stress, which are typical of the surficial sediment habitat and they appeared to be principally dependent on the algal resource.     

Transmission of symbiotic dinoflagellates through the sexual cycle of the host scyphozoan Linuche unguiculata

Intracellular symbiotic dinoflagellates are associated with the tropical scyphozoan Linuche unguiculata (Swartz, 1788) throughout all stages of the host's life cycle. During sexual reproduction, eggs are released in mucus strands that contain symbiotic dinoflagellates. Fertilization and development take place externally in the water column. Epifluorescence and transmission electron microscopy showed that unfertilized eggs did not contain intracellular algae, but that infection of the developing embryo was generally successful by the 128-cell stage (10 h after fertilization at 23° C). However, experiments with artificially provided Cellufluor-labeled algae demonstrated that older embryos and planulae could be infected by algae through at least 24 h post-fertilization, indicating that the L. unguiculata symbiosis represents a semi-closed system. This novel mode of symbiont acquisition results in most sexually-produced offspring becoming infected with maternally-transmitted algae during early development, but allows for acquisition of non-maternally-provided algae later in development. Most of the algal symbionts during the early stages of embryonic and larval development are located within ectodermal cells. This is in contrast to the other life-cycle stages of L. unguiculata (i.e., scyphistoma, medusa, ephyra), where symbionts are found within the gastrodermis of the host.     

Influence of algal and suspended sediment concentrations on the feeding physiology of the hard clam Mercenaria mercenaria

Short-term laboratory feeding experiments were conducted to determine the response of the hard clam Mercenaria mercenaria (L.) (32 mm in mean shell length) to increasing sediment concentrations. Clams were fed mixed suspensions of Pseudoisochrysis paradoxa (50 and 150 cells l^-1) and bottom sediments (0 to 44 mg l^-1). Algal ingestion rate deelined with increasing sediment loads. This resulted primarily from a reduction in clearance rate, which declined by 0.08 l h^-1 g^-1 (1.3%) for every 1 mg l^-1 increase in sediment load. This reduction was of similar magnitude for juvenile (13 mm) clams. At the algal concentrations tested, pseudofaeces production was intermittent and inconspicuous below about 10 mg silt l^-1. Loss of algae in pseudofaeces increased with increasing sediment loads; however, even at the highest silt and algal concentrations, clams lost a maximum of only 18% of the algae cleared from suspension. Thus, pseudofaeces production is not expected to cause significant loss of algal food at the sediment concentrations normally encountered in the natural environment ( ca 40 mg silt l^-1). Absorption rate of total organic matter remained constant, at least up to silt concentrations of 20 mg l^-1. Experiments using dual ⁵¹Cr:¹⁴C-formaldehyde-labelled sediment indicated that clams were able to counteract the dilution of algae by absorbing a considerable fraction (21 to 22%) of detrital sedimentary organics. Absorption efficiency of pure P. paradoxa ranged from 82% at 50 cells l^-1 to 58% at 150 cells l^-1. Integration of physiological rate measurements suggests that at moderate to high algal concentrations (300 g Cl^-1), growth improvement by the addition of silt, documented in mussels, surf clams and oysters, is unlikely to occur in M. mercenaria. It is suggested that a suspension-feeding bivalve's success in maximizing its energy gain in a turbid environment depends on the combination of two features: a high selection efficiency and a high rate of pseudofaeces production. It is proposed that species which regulate ingestion primarily by producing pseudofaeces are better adapted to cope with high suspended sediment loads than species such as M. mercenaria, which control ingestion mainly by reducing clearance rate.Contribution No. 451 from the Marine Sciences Research Center, State University of New York at Stony Brook, USA     

The spring phytoplankton bloom in Lindåspollene,a land-locked Norwegian fjord. II. Biomass and activity of net- and nanoplankton

From February 24 to April 24, weekly samples were collected at fixed depths at one station in Lindåspollene, a land-locked Norwegian fjord. Adenosine triphosphate (ATP), chlorophyll a, phaeophytin, ¹⁴C assimilation, and respiratory activity [electron transport system (ETS) activity] were measured in the net- (>30 m) and nanoplankton. Netplankton contained on the average 48% of the total chlorophyll a and 56% of the ATP, but contributed only 7% to the total carbon assimilation and 11% to the ETS activity. The assimilation numbers for net- and nanoplankton ranged from 0 to 1.2 and from 1.5 to 13.2, respectively. At the oxygen/hydrogen sulphide interface, high concentrations of ATP, but not of chlorophyll a, were found in the nanoplankton fraction. Netplankton algae grew actively only in the first phase of the bloom, and nanoplankton predominated later, apparently due to low nutrient concentrations. During the bloom, Skeletonema costatum made up the main part of the biomass. The number of cells in the chains decreased throughout the bloom, possibly reflecting the lowered silicate content. It appeared that only nanoplankton were grazed by zooplankton, while netplankton sank to the bottom and represented input to the benthos.     

Eulerian sampling of zooplankton from Marseilles' Vieux Port over a 24 h period

A 24 h continuous study of hydrological parameters and zooplanktonic populations was carried out in Marseilles' Vieux-Port, a semi-closed area supposed to be a fairly homogeneous body of water. Sampling was performed in spring 1980 with a pump system. Samples were taken every 30 min over a period of 24 h, during which time only slight temperature variations were recorded (min.=14.5°C, max.=15.1°C); salinities were high and fairly stable (min.=37.49, max.=37.63%.). It can thus be assumed that the water was homogeneous. Concentrations of suspended particulate matter were high and fairly stable (x = 11.8 mg 1^-1). In most samples, nitrate levels were fairly low (x = 0.84 g-at 1^-1); conversely, phosphate contents fluctuated greatly (min.=0.24 g-at 1^-1, max.=2.24 g-at 1^-1). As a result of these fluctuating nutrient-salt values, the N:P ratios were often unbalanced (between 0.5 and 2.0). Detergent values were low (often less than 0.2 ppm). Zooplanktonic populations were made up of a few eurybiotic species, the most thriving of which were the cladoceran Podon polyphemoides and the copepod Acartia clausi. These two species perform nychthemeral migrations towards the surface: P. polyphemoides during the day and A. clausi at night. As a result of these opposite patterns of migrations, the planktonic biomass remained fairly stable near the surface. There were also some meroplanktonic species (especially cirripede larvae) and a small number of other copepods present. This study revealed a regular hydrological and faunal cycle with a return to initial conditions at the end of the 24 h period.     

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).