The size and function of the internal inorganic carbon pool of the foraminifer Amphistegina lobifera

The existence of an internal inorganic carbon pool in the perforate foraminifer Amphistegina lobifera, as suggested recently (ter Kuile and Erez 1987), has been established by direct measurements using a new ¹⁴C tracer method. The imperforate species Amphisorus hemprichii does not contain such a pool. The size of the pool in A. lobifera is proportional to its calcification rate and approximately equals the amount of carbon incorporated into the skeleton during 24 h. Time course experiments show that inorganic carbon (Ci) is photoassimilated at constant rates by the algal symbionts, that the pool is filled to maximum capacity in ca. 24 h, and that Ci incorporation into the skeleton starts only after the pool is filled up. During the chase phase of pulsechase experiments, all ¹⁴C initially residing in the pool is transferred to the skeleton, indicating that the pool serves for calcification and not for photosynthesis. Uptake of Ci into the pool occurs only in the light, indicating that energy may be required for this process. Furthermore, calculations of the Ci concentration inside the pool suggest that it is higher by 2 to 3 orders of magnitude compared to seawater concentration, suggesting that its accumulation is an energy dependent process.     

Mechanisms for the uptake of inorganic carbon by two species of symbiont-bearing foraminifera

The mechanisms for uptake of inorganic carbon (Ci) for photosynthesis and calcification of a perforate foraminifer, Amphistegina lobifera Larsen, and an imperforate species, Amphisorus hemprichii Ehrenberg, from the Gulf of Eilat, Red Sea were studied in 1986–1987 using ¹⁴C tracer techniques. Total Ci uptake of A. lobifera and photosynthetic carbon uptake of A. hemprichii fit the Hill-Whittingham equation that describes the overall rate of enzymatic reactions that are provided with their substrate through a diffusion barrier. This suggests that diffusion is the rate limiting step for total Ci uptake in A. lobifera. Photosynthesis by the isolated symbionts and uptake of CO₃ ^2- for calcification obey Michaelis-Menten kinetics indicating that enzymatic reactions determine the rate of the separate processes. Both photosynthesis and calcification can be inhibited without affecting each other. Calcification rates in A. lobifera were optimal at Ca levels around normal seawater concentration and were sensitive to inhibitors of respiratory adenosine triphosphate (ATP) generation and Ca-ATP-ase. This indicates that Ca uptake is also active. Calcification rates of A. hemprichii increased linearly as a function of external Ci concentration over the entire experimental range (0 to 4 mM Ci). In contrast, photosynthetic rates showed Hill-Whittingham type kinetics. The dependence of calcification on the CO₃ ^2- concentration was also linear, suggesting that its diffusion is the rate limiting step for calcification in A. hemprichii. Increasing Ca concentrations yielded higher calcification rates over the entire range measured (0 to 40 mM Ca). Calcification in A. hemprichii was less sensitive to inhibitors of ATP generation than in A. lobifera, suggesting that in A. hemprichii energy supply is less important for this process.     

Nutritional and related experiments on laboratory maintenance of three species of symbiont-bearing,large foraminifera

Factors were examined that affect survival and growth of two common species of large foraminifera from the Red Sea,Amphisorus hemprichii Ehrenberg andAmphistegina lobifera Larsen, 1976. The former is host for dinoflagellate and the latter for diatom zooxanthellae. Experimental conditions were modeled on conditions at 25 m during spring at Wadi Taba, Gulf of Elat, Israel, the season and site where the experimental organisms were collected between 1983 and 1988. The two species responded quite differently in nutritional experiments.A. hemprichii grew, on average, 0.270 mm in diameter in 3 mo on a diet ofNitzschia subcommunis Hustedt,Chlorella sp. (clone AT) orCylindrotheca closterium Rabenhorst isolated from their native habitat. Unfed controls did not grow. In contrast, unfed populations ofA. lobifera grew as well or better than those that were fed unialgal diets. Growth of both species was enhanced on particular mixed algal diets. Both species required photosynthetically active symbionts. Even when fed weekly and supplied with nutrients, neither species survived in the dark. All individuals ofA. hemprichii died after 8 wk incubation in the dark;A. lobifera survived longer, but all were dead by 13 wk. The highest growth rate ofA. hemprichii (0.037 mm wk^–1) was obtained when they were fed, the medium was enriched, and the medium was changed weekly. All other conditions being the same, growth rate dropped to 0.009 mm wk^–1 when the medium was changed every 3 wk. In contrast,A. lobifera grew fastest when the medium was changed every 3 wk. Food or enrichment with nitrate or phosphate did not stimulate growth (0.03 mm wk^–1) over that of the controls. Specimens ofMarginopora kudakajimensis Gudmundsson from Japan, another dinoflagellate-bearing species, were also tested. They grew best (0.02 mm wk^–1) when cultured in light, in media enriched with nitrate and phosphate changed weekly, and fed. All three species withdrew nitrate and phosphate from the medium in chemostat experiments.     

Photosynthetic utilisation of inorganic carbon by seagrasses from Zanzibar, East Africa

Photosynthetic rates of eight seagrass species from Zanzibar were limited by the inorganic carbon composition of natural seawater (2.1 mM, mostly in the form of HCO₃ ⁻), and they exhibited more than three time higher rates at inorganic carbon saturation (>6 mM). The intertidal species that grew most shallowly, Halophila ovalis, Halodule wrightii and Cymodocea rotundata, showed the highest affinity for inorganic carbon (K _1/2 = ca. 2.5 mM), followed by the subtidal species (K _1/2 > 5 mM). Photosynthesis of H. wrightii, C. rotundata, Cymodocea serrulata and Enhalus acoroides was >50% inhibited by acetazolamide, a membrane-impermeable inhibitor of carbonic anhydrase, indicating that extracellular HCO₃ ⁻ dehydration is an important part of their inorganic carbon uptake. Photosynthetic rates of H. wrightii, Thalassia hemprichii, Thalassodendron ciliatum, C. serrulata and E. acoroides were strongly reduced by changing the seawater pH from 8.2 to 8.6 in a closed system. In H. ovalis, C. rotundata and Syringodiumisoetifolium, photosynthesis at pH 8.6 was maintained at a higher level than could be caused by the ca. 30% CO₂ concentration which remained in the closed experimental systems at that pH, pointing toward HCO₃ ⁻ uptake in those species. It is suggested that the ability of H. ovalis and C. rotundata to grow in the high, frequently air-exposed, intertidal zone may be related to a capability to take up HCO₃ ⁻ directly, since this is a more efficient way of HCO₃ ⁻ utilisation than extracellular HCO₃ ⁻ dehydration under such conditions. The inability of all species to attain maximal photosynthetic rates under natural conditions of inorganic carbon supports the notion that seagrasses may respond favourably to any future increases in marine CO₂ levels. Received: 19 March 1997 / Accepted: 31 March 1997     

Zooxanthellae providing assimilatory power for the incorporation of exogenous acetate in Heteroxenia fuscescens (Cnidaria: Alcyonaria)

The soft coral Heteroxenia fuscescens (Ehrb.) and its isolated zooxanthellae (endosymbiotic dinoflagellates) were investigated with particular regard to uptake and utilization of exogenously supplied ¹⁴C-acetate in the light and in the dark. The incorporation of ¹⁴C from ¹⁴C-acetate into the host tissue and into the zooxanthellae was consistently much higher in the light than in the dark. The incorporated ¹⁴C-acetate was rapidly metabolized by the host and algae and was recovered from different assimilate fractions. The major proportion of radiocarbon from metabolized ¹⁴C-acetate was located in host tissue. The CHCl₃-soluble fraction composed of diverse lipids showed the strongest ¹⁴C-labelling. Zooxanthellae isolated prior to incubation accounted for about 80% of the acetate incorporation recorded for zooxanthellae in situ (in vivo). It is concluded from a comparison of acetate incorporation and conversion under light and dark conditions that most of the lipid reserve of the host tissue originates from fatty acids, which are synthesized within the algal symbionts and are then translocated to the heterotrophic partner via extrusion. The acetate units needed for lipid synthesis are obtained by absorption of free acetate from dissolved organic matter (DOM) in the seawater as well as by photosynthetic assimilation of inorganic carbon. Thus, in H. fuscescens, lipogenesis is operated as a light-driven process to which the zooxanthellae considerably contribute assimilatory power by performing fatty acid synthesis and translocation of lipid compounds to their intracellular environment (host cell). A metabolic scheme is proposed to account for the different pathways of carbon conversion observed in H. fuscescens. The incubations took place in August 1980 and the analytical part from October 1980 to January 1984.     

Assessment of simultaneous uptake of nitrogenous nutrients (15N) and inorganic carbon (13C) by natural phytoplankton populations

The simultaneous uptake of nitrogenous nutrients and inorganic carbon was measured in shipboard incubations of natural phytoplankton populations, using tracer additions of ¹³C-bicarbonate and ¹⁵N-labelled nitrogenous substrates. From March 1991 through March 1992, three stations on the Scotian Shelf (eastern Canada) were sampled monthly at ten depths in the euphotic zone. Additions of labelled nitrogen compounds ranged between 0.5 and 98% of ambient concentrations. Most of the C/N (at/at) uptake ratios were lower than the Redfield ratio, suggesting that nitrogen was not limiting. The fixation of carbon with and without addition of nitrate, ammonium or urea was generally similar. Some samples presented significant differences in carbon uptake rate between the four treatments, but these differences were not related to nitrogen enrichment (percent or nitrogen species). Given these results, the double-labelling method appears to be a reliable tool for measuring the simultaneous uptake of carbon and nitrogen by natural phytoplankton.     

Respiration,photosynthesis and carbon metabolism in planktonic ciliates

Release of¹⁴C-labelled carbon dioxide from uniformly labelled cells was used to measure respiration by individual ciliates in 2-h incubations in 1989 and 1990. In a strictly heterotrophic ciliate,Strobilidium spiralis (Leegaard, 1915), release of labelled carbon dioxide was equivalent to ca. 2.8% of cell C h^–1 at 20°C, and there was no difference between rates in the dark and light. In the chloroplast-retaining ciliatesLaboea strobila Lohmann, 1908,Strombidium conicum (Lohmann, 1908) Wulff, 1919 andStrombidium capitatum (Leegaard, 1915) Kahl, 1932, release of labelled carbon dioxide was less in the light than in the dark in experiments done at 15°C. InL. strobila release of radiolabel as carbon dioxide was equivalent to ca. 2.4% of cell C h^–1 in the dark but ca. 1% at 50µE m^–2 s^–1, an irradiance limiting to photosynthesis. InS. conicum release of radiolabel as carbon dioxide was equivalent to ca. 4.4% of cell C h^–1 in the dark, but at an irradiance saturating to photosynthesis (250 to 300µE m^–2 s^–1) there was no detectable release of labelled carbon dioxide. InS. capitatum release of radiolabel as carbon dioxide was equivalent to ca. 4.3% of cell C h^–1 in the dark but at an irradiance saturating to photosynthesis was ca. 2.4% of cell C h^–1. These data, combined with data from photosynthetic uptake experiments, indicate that¹⁴C uptake underestimates the total benefit of photosynthesis by 50% or more in chloroplastretaining ciliates.Contribution no. 7510 from the Woods Hole Oceanographic Institution     

Photosynthetic carbon acquisition in the red algaGracilaria conferta

Photosynthetic properties of the common red algaGracilaria conferta, collected from the eastern Mediterranean Sea were investigated in 1989, in order to begin evaluating its adaptative strategies with regard to the inorganic carbon composition of seawater, and to test whether the alleged C₄ photosynthesis of anotherGracilaria species is common within the genus. Net photosynthetic rates ofG. conferta were, under ambient conditions of inorganic carbon (ca. 10µM, CO₂ and 2.2 mM HCO ₃ ^- ), not sensitive to O₂ over the range 10 to 300µM, and the CO₂ compensation point was low (ca. 0.005µM). Ribulose-1,5-bisphosphate carboxylase/oxygenase was the major carboxylating enzyme, with a crude extract activity of 175µmol CO₂ g^–1 fresh wt h^–1 while phosphoenolpyruvate carboxylase and phosphoenolpyruvate carboxykinase were present at 70 and 20%, respectively, of that activity. No activities of the decarboxylases NAD-and NADP-malic enzyme could be detected. The¹⁴C pulse-chase incorporation pattern showed thatG. conferta fixes inorganic carbon via the photosynthetic carbon reduction cycle only, with no evidence for photosynthetic C₄ acid metabolism. Photosynthesis at the natural seawater pH of 8.2 was, at 25°C and saturating light, saturated at the ambient inorganic carbon concentration of 2.5 mM. It is proposed that, under ambient inorganic carbon conditions, a CO₂ concentrating system other than C₄ metabolism provides an internal CO₂ concentration sufficient to suppress the O₂ effect on ribulose-1,5-bisphosphate carboxylase/oxygenase and, thus, on photorespiration, in a medium where the external free CO₂ concentration is lower than theK _m(CO₂) of the carboxylating enzyme. Since inorganic carbon, under natural saturating light conditions, seems not to be a limiting factor for photosynthesis ofG. conferta, it likely follows that other nutrients limit the growth of this alga in nature.     

Compartmentation and turnover of organic carbon in the Staghorn coral Acropora formosa

Four colonies of Acropora formosa were incubate with Na₂ ¹⁴CO₃ for separate 2 h periods within a 24 h period, and then returned to the reef from which they were collected. Terminal branches were collected at intervals over the following 5 d and analysed for radioactivity associated with the skeleton and certain organic pools. Colonies incubated at night showed little or no loss of fixed radioactivity during the 5 d on the reef. However, 50–60% of photosynthetically-fixed ¹⁴C was lost from the terminal branches during the first 40 h on the reef. This loss of radioactivity probably resulted from release of mucus and dissolved organic carbon from the coral tissues. Most of the loss of photosynthetically-fixed ¹⁴C was due to decrease in the radioactivity of lipids (80% of the total ¹⁴C loss) and methanol-water soluble compounds. Determination of any sequencing in metabolic compartments was made difficult by the rapidity with which ¹⁴C dissappeared from most of the metabolic pools measured. ¹⁴C was incorporated into the skeleton throughout the 5 d on the reef, although the rate of incorporation was very low in colonies which had been incubated with Na₂ ¹⁴CO₃ at night.     

Calcification in the staghorn coral Acropora acuminata: Variations in apparent skeletal incorporation of radioisotopes due to different methods of processing

Pieces of branch from the staghorn coral Acropora acuminata were incubated with ⁴⁵CaCl₂ and NaH¹⁴CO₃ under identical conditions in the light or in the dark. Specimens were then processed in different ways. All specimens were placed in N KOH to digest tissues. Some were placed in KOH immediately after incubation; others were placed in KOH after 2 h washing, or after 2 h extraction with methanol-chloroformwater. Specimens were washed in running fresh water or running seawater; some were killed in liquid N₂ before washing. Radioactivity associated with skeleton and tissues was determined. The method of processing profoundly affected the results. In dark incubations, there was up to a four-fold difference in apparent skeletal incorporation of ⁴⁵Ca⁺⁺ between average values obtained for the different treatments. For ¹⁴C incorporation, there was a difference of up to 2.5 times. In light incubations, skeletal incorporation of both radioisotopes showed a two-fold difference between high and low average values obtained for the different treatments.     

Effect of boundary layer transport on the fixation of carbon by the giant kelp Macrocystis pyrifera

The uptake of inorganic carbon into the thallus of Macrocystis pyrifera (L.) C. Ag. requires first that the inorganic carbon pass through the water medium to the plant surface. This transfer of inorganic carbon to the thallus must take place through a boundary layer. Experiments in water tunnels indicate that the boundary layer adjacent to the M. pyrifera blade may be turbulent in water speeds as low as 1 cm sec^-1. Photosynthetic output of the blade can be increased by a factor of 300% by increasing water speeds over the blade surface from 0 to 4 cm sec^-1. This is consistent with a decrease in the thickness of the boundary layer. Above 4 cm sec^-1, the assimilation of carbon was limiting. The assimilation of carbon is generally known to follow Michaelis-Menten-like kinetics. Combining the two uptake steps into an overall model of carbon uptake agrees well with photosynthetic data obtained from M. pyrifera under varying conditions of water speed and bicarbonate concentrations in the laboratory. The ecological and morphological consequences of these findings are discussed.     

A new method for estimating phytoplankton growth rates and carbon biomass

A new method is described for the determination of phytoplankton growth rates and carbon biomass. This procedure is easy to apply and utilizes the labeling of chlorophyll a (chl a) with ¹⁴C. Pure chl a is isolated using two-way thin-layer chromatography, and the specific activity of chl a carbon is determined. Data from laboratory cultures indicate that the specific activity of chl a carbon becomes nearly equal to that of total phytoplankton carbon in incubations lasting 6 to 12 h and can be used to calculate phytoplankton growth rates and carbon biomass. Application of the method to the phytoplankton community in an eutrophic estuary in Hawaii indicates that the cells are growing with a doubling time of about 2 d and that about 85% of the particulate carbon consists of phytoplankton carbon.     

Distinguishing modes of dissolved organic carbon production in marine macrophytes by tracer kinetic analysis

Tracer kinetic analysis of radioisotope incorporation into dissolved organic compounds reveals two distinct patterns of photosynthate release by macroalgae. In experiments employing Sargassum lacerifolium, dissolved organic carbon was produced at a constant rate during light incubations. Steady state rates of production were never achieved in experiments employing either Ecklonia radiata (Turn.) J. Agardh. or Ulva lactuca L. Analysis of the time-varying radioactivity curves obtained in experiments using these algae always resulted in models consistent with dissolved organic carbon production being an autocatalytic process. Preincubation of U. lactuca in the dark resulted in a diminished (ca. 40%) rate of dissolved organic carbon production during the subsequent light incubations. In no case did the radioisotope content of the dissolved organic carbon approach a limiting value, indicating that in contrast to phytoplankton, uptake rates of photosynthate by macroalgae are always less than the rates of production.     

Variations in the progress of 14C uptake as a source of error in estimates of primary production

The progress curves of ¹⁴C retention for samples of phytoplankton from the Irish Sea incubated at contrasting light intensities have been obtained by two methods. The first method (A) involved the incubation of the samples for various periods up to 6 h, while the second method (B) consisted of making a series of short-term incubations over the same 6 h period. Over this period, the cumulative uptake was tenerally less when estimated by Method A than by Method B. The difference was greater in the samples incubated at the lower light intensity, the light history of the samples having no effect on the difference. The differences has a kinetic basis, with two combinations of progress curves obtained by use of the two methods. The first combination was associated with samples collected in the early morning, while the second combination was exhibited by samples taken in the afternoon irrespective of sampling depth. In certain samples, no increase in the ¹⁴C retained by the cells as measured by Method A was observed after 4 h. The cumulative retention of ¹⁴C by the cells after 2 h was generally greater when estimated by Method A than by Method B, this situation being reversed after 4 h. This reversal indicated a change in uptake kinetics between 2 and 4 h and it is suggested that this interval represents the time necessary for the ¹⁴C to work through the cellular pool of carbon. The findings are discussed in relation to the methodology for obtaining both estimates of primary production and ¹⁴C uptake-light intensity curves for marine phytoplankton.     

Regulation of the Si and C uptake and of the soluble free-silicon pool in a synchronised culture of<Emphasis Type="Italic"> Cylindrotheca fusiformis</Emphasis> (Bacillariophyceae): effects on the Si/C ratio

Silicon and carbon uptake rates were studied over a 24 h light/dark cycle in a synchronised culture of the marine diatom Cylindrotheca fusiformis (Reimann et Lewin) using ³²Si and ¹⁴C. The silicic acid uptake rate per cell (^cSi) varied between 1.2 and 20.0 fmol Si cell^–1 h^–1 and was closely correlated to the G2+M phase of the cell cycle. A linear and significant relationship was determined between the percentage of cells present in G2+M and ^cSi. Evolution of the soluble free-silicon pool was studied simultaneously. The concentration of the total soluble free pool of silicon (Q^PSi) varied from 1% to 7% of the total silicon content. A significant difference of 1.5 fmol Si cell^–1 between Q^PSi and the labelled free pool (Q^npSi) was measured, indicating the presence of an unlabelled fraction of the pool. The concentration of Q^npSi was around 1.0 fmol Si cell^–1 prior to cell division and did not change as a function of ^cSi, which indicated a feedback mechanism coupling uptake into the free pool and incorporation into the frustule. In parallel, ¹⁴C uptake variation (^cC) was measured during the division of the population. The value of ^cC varied between 0.44 and 0.78 pmol C cell^–1 h^–1 and appeared to be maximal when cells were in the G1 phase. This variation of ^cC marginally affected the total carbon content of the cells (Q^TC) in comparison with the light/dark cycle. The variations in the Si/C ratio, from 0.021 to 0.046, demonstrated the different control mechanisms of Si and C metabolisms during the course of the cell- and photocycle.Communicated by S.A. Poulet, Roscoff     

A reevaluation of the role of glycerol in carbon translocation in zooxanthellae-coelenterate symbiosis

Glycerol has been traditionally viewed as the main form of carbon translocated from zooxanthellae to the coelenterate host. Most of this glycerol was postulated to be used by the coelenterate host for lipid synthesis. Recent work suggests that large amounts of photosynthetically fixed carbon is synthesized into lipid in the algae, and then translocated as lipid droplets to the host. These two hypotheses of carbon translocation are not mutually exclusive, but to reconcile them the role of glycerol must be reevaluated. In this study the short term metabolic fate of uniformly labelled ¹⁴C-glycerol, ¹⁴C-bicarbonate, and ¹⁴C-acetate was examined in zooxanthellae and coelenterate host tissue isolated from Condylactis gigantea tentacles. When host and algal triglycerides, synthesized during 90-min light and dark incubations in ¹⁴C-bicarbonate and ¹⁴C-acetate, were deacylated, more than 80% of the activity was found in the fatty acid moiety. In contrast, triglycerides isolated from zooxanthellae and coelenterate host tissue incubated in ¹⁴C-glycerol in the dark for 90 min were found to have more than 95% of their radioactivity in the glycerol moiety. During the 90-min ¹⁴C-glycerol incubations in the light, the percentage of radioactivity in the fatty acid moiety of zooxanthellae triglycerides increased to 37%. The percentage of radioactivity in the host tissue triglycerides fatty acid moiety stayed below 5% during the 90-min ¹⁴C-glycerol incubations in the light. These results show that neither the zooxanthellae nor the host can rapidly convert glycerol to fatty acid. Radioactivity from ¹⁴C-glycerol, which does eventually appear in host lipid, may have been respired to ¹⁴CO₂, then photosynthetically fixed by the zooxanthellae and synthesized into lipid fatty acid.     

Photosynthesis and carbon storage between tides in a brown alga, Fucus vesiculosus

Intertidal macroalgae may spend a significant part of their lives in air. During photosynthesis in air, they encounter much lower concentrations of inorganic carbon than in seawater. Because they accumulate inorganic carbon from seawater, we investigated whether they similarly accumulate it from air. We measured photosynthesis in the intertidal species Fucus vesiculosus L. during 1990 and 1991 with a gas-phase O₂ electrode or CO₂-exchange apparatus in air and with a liquid-phase O₂ electrode in seawater. Maximum rates were rapid and similar in air and seawater regardless of the method. Tissue from seawater could carry on photosynthesis in CO₂-free air, indicating that carbon was stored in the tissue. After 2 h, this store was depleted and photosynthesis ceased. Supplying CO₂ in air replenished the store. Under identical conditions, terrestrial C₃ and C₄ species showed no evidence of this store, but a CAM (crassulacean acid metabolism) species did. However, in contrast to the CAM behavior, F. vesiculosus did not store CO₂ significantly in the dark. We found a small acid-releasable pool of carbon in the tissue that disappeared as photosynthesis depleted the carbon store. However, the pool was too small to account for the total carbon stored. While CO₂ was being acquired or released from the store in the light, photosynthesis was not inhibited by 21% O₂. These results indicate that there are two parallel paths for the supply of CO₂ to photosynthesis. The first depends on inorganic carbon in seawater or in air and supports rapid photosynthesis. The second involves CO₂ slowly released from an organic intermediate. The release protects CO₂ fixation from the inhibitory effects of 21% O₂. Photosynthesis in F. vesiculosus thus appears to be C₃-like in its rapid fixation of CO₂ from a small inorganic pool into phosphoglycerate. However, it is C₄-like in its pre-fixation of carbon in an organic pool in the light, and is CAM-like in its ability to slowly use this pool as a sole source of CO₂. The organic pool may serve to protect photosynthetic CO₂ fixation against the inhibitory effects of O₂ in air and in the boundary layer in seawater. Received: 6 March 1998 / Accepted: 16 October 1998     

Effect of copper and cadmium on carbon assimilation and uptake of metals by algae

Two species of blue green algae Spirulina platensis and Anacystis nidulans grown in artificial aqueous media were treated with Cu and Cd in concentrations of 0.01, 0.1, 1.0 and 10 ppm to study carbon assimilation and Chlorophyll (Chl) A content. The species were treated with concentrations of 0.1, 0.5, 1.0, 5.0 and 10.0 ppm to study the uptake of metals with exposure time. Carbon assimilation and Chl A content showed responses proportional to the concentration in the general form y = K + n ln C, where C is the concentration of metal in ppm, while in case of uptake the relation was y = KC”; (where C is the molar concentration x 10^‐6 of the metal). The n values in case of uptake was found to be < 1 indicating a non‐Langmuir type of sorption. The concentration factors of metals decreased with metal concentration in the medium.     

Significance of active and passive depuration in the clearance of naphthalene from the tissues of Hemigrapsus nudus (Crustacea: Decapoda)

Photosynthate incorporation into lipids, low molecular weight compounds, polysaccharides and proteins by individual phytoplankton species isolated from natural populations is described. This sensitive method uses serial solvent extraction and liquid scintillation counting and gives results indentical to those obtained from filtering large numbers of cells from suspension. The time course of incorporation of ¹⁴C into these polymers for algae isolated from estuarine and coastal populations shows (i) considerable differences in the carbon metabolism among species, (ii) the pattern of incorporation by any individual species may not reflect that of the phytoplankton community and (iii) significant reallocation of cell carbon among carbon pools and net protein synthesis at night. This technique permits the in-situ carbon metabolism of individual species to be examined.     

Carbon fixation and analysis of assimilates in a coral-dinoflagellate symbiosis

Freshly collected pieces of the hermatypic coral Acropora cf. scandens containing dinoflagellate endosymbionts (presumably Gymnodinium microadriaticum) were allowed to assimilated ¹⁴C from H¹⁴CO ₃ ^- in the light and in the dark. Time-dependent carbon uptake resulted in intense ¹⁴C-labelling of ethanol-soluble as well as of insoluble assimilates. About forty ¹⁴C-labelled assimilates have been identified. Polymeric (ethanol-insoluble) compounds achieve about 30% of total radiocarbon incorporation after 60 min incubation. Kinetics of ¹⁴C-labelling of single assimilates are analyzed. Percentages of typical photosynthates in the soluble fraction undergo characteristic time-dependent changes. Lipids proved to be the main accumulation products of carbon assimilation by incorporating more than 50% of ¹⁴C after 60 min photosynthesis. The data indicate that low-molecular weight photosynthates such as ¹⁴C-glycerol and ¹⁴C-glucose are rapidly converted to constituents of the polymeric fraction(s) of the coral. Besides peptides, polysaccharides, and lipophilic substances, considerable amounts of ¹⁴C are confined to skeletal CaCO₃ of the coral. The results are discussed with respect to trophic and metabolic interrelationships between the autotrophic dinoflagellates and the A. cf. scandens tissues.