Calcification in the maerl coralline alga Phymatolithon calcareum: Effects of salinity and temperature

The coralline alga Phymatolithon calcareum was dredged from 13 m in the Kattegatt, Baltic Sea, in December, 1980, and its rate of calcification was measured by ⁴⁵Ca⁺⁺-uptake methods. Light-saturated calcification rates at 5°C ranged from 15.8 g CaCO₃ g^-1 dry wt h^-1 for the basal parts of the plants to 38.7 g CaCO₃ g^-1 dry wt h^-1 for the tips. These age gradients were not apparent when calcification rates were expressed on the basis of surface area. Experiments with salinity (10, 20, 30) and temperature (0°, 5°, 10°, 20°C) indicated that optimum conditions for calcification were at 30 S and at temperatures above 10°C. Salinity had a greater influence on calcification rate than did temperature, and there was a positive relationship between salinity and calcification rate at all temperatures. In 6 mo old cultures, salinity was again the important factor, with all plants remaining healthy at 30 except those at the highest temperature (20°C). These trends, and the low calcification rates at 10S (4.6 g CaCO₃ g^-1 dry wt h^-1 at 5°C to 8.6 g CaCO₃g^-1 dry wt h^-1 at 20°C) suggest that low salinity may be the explanation for the general absence of P. calcareum from the brackish waters of the Baltic Sea. Short-term experiments in which salinity was kept constant while Ca⁺⁺ concentration was altered, and experiments in which salinity was varied and Ca⁺⁺ concentration kept constant, suggest that it is the calcium ion concentration and not salinity per se which affects calcification rates.     

Cohabitation of a coral reef sponge and a colonial scyphozoan

A sensitive experimental protocol using cloned corals (hereafter microcolonies) of the branching scleractinian coral Stylophora pistillata and ⁴⁵Ca has been developed to enable reproducible measurements of physiological and biochemical mechanisms involved in calcium transport and compartmentalization during coral calcification. Cloned S. pistillata microcolonies were propagated in the laboratory from small fragments of parent colonies collected in 1990 in the Gulf of Aqaba, Jordan. Cloned microcolonies have several intrinsic properties that help to reduce unwanted biological variability: (1) same genotype; (2) similar sizes and shapes; and (3) absence of macroscopic boring organisms. Errors specifically associated with long-standing problems to do with isotopic exchange were further reduced by producing microcolonies with no skeletal surfaces exposed to the radioisotope-labelled incubation medium. The value of the technique resides principally in its superior ability to elucidate transportation pathways and processes and not in its ability to quantitatively estimate calcium deposition by corals in nature. We describe here a rapidly exchangeable calcium pool in which up to 90% of the radioactive label taken up during incubations is located. This pool (72.9±1.4 nmol Ca mg^-1 protein) is presumably located within the coelenteric cavity as suggested by the following: (1) it has 4-min half-time saturation kinetics; (2) the accumulation of calcium is linearly correlated with the calcium concentration of sea-water; and (3) its insensitivity to metabolic and ion transport inhibitors indicate that membranes do not isolate this compartment. Washout of this large extracellular pool greatly improved estimates of calcium deposition as evidenced by 10 to 40% reduction in coefficients of variation when compared with previous ⁴⁵Ca²⁺ methods described in the literature. Comparisons of calcification measurements simultaneously carried out using the alkalinity anomaly technique and the ⁴⁵Ca protocol described here show that the correlation coefficient of both techniques is close to 1. Unlike previous reports, our ⁴⁵Ca²⁺-derived measurements are slightly lower than those computed from the alkalinity depletion technique.     

Respiratory quotient and calcification of Nautilus macromphalus (Cephalopoda: Nautiloidea)

Respiration and calcification were investigated in the ectocochleate cephalopod Nautilus macromphalus Sowerby. Specimens were collected off New Caledonia, in October 1991, and kept at the Nouméa Aquarium until December 1991. The respiratory quotient and calcification rate of 5 individuals were measured during 14 short term incubations (63 to 363 min). Oxygen uptake was recorded with a polarographic oxygen sensor. CO₂ flux and calcification were calculated from changes in pH and alkalinity (alkalinity-anomaly technique). Several methods were used to compute the respiratory quotient (RQ); a functional regression indicated an RQ of 0.74. CaCO₃ exchange rates were linearly related to respiratory quotient, calcification occurring in individuals with a low RQ. CaCO₃ uptake from the surrounding water was noncontinuous. From the highest CaCO₃ uptake, maximum growth rate was estimated as 7.1 mg shell wt h^- (=61 g yr^-1).     

Photosynthesis and amelioration of desiccation in the intertidal saccate alga Colpomenia peregrina

Rates of gross photosynthesis for the intertidal saccate alga Colpomenia peregrina (Sauv.) Hamel were determined under submersed and emersed conditions. Maximal photosynthetic rates were lower than for most seaweeds but comparable with other saccate members of the genus. By fitting the data to a hyperbolic tangent function, maximal photosynthetic rates were estimated to be 5.29 mmol CO₂ m^-2 h^-1 under submersed conditions and 2.06 mmol CO₂ m^-2 h^-1 under emersed conditions. I_k for submersed thalli was 69.1 E m^-2 s^-1, wherea for emersed thalli it was 149.0 E m^-2 s^-1, or 2.2 times higher. At low tide in the field and under saturating irradiance, carbon from seawater retained within the thallus cavity was assimilated at 0.9 mmol CO₂ m^-2 h^-1. In the laboratory under emersed conditions, carbon from this source was taken up at 0.6 mmol CO₂ m^-2 h^-1 at 20°C and at 0.34 mmol CO₂ m^-2 h^-1. Retained seawater also greatly reduced drying under desiccating conditions. Experimental thalli from which seawater had been removed lost thallus water continuously throughout the drying period (120 min). On the other hand, control, thalli lost water for the first 15 min, after which no further water loss occurred. At the termination of the experiment, control thalli had lost 7.2% of their water, whereas experimental thalli had lost 39.2%. Desiccation affected the emersed photosynthetic rate of experimental and control thalli. Emersed photosynthetic rates for thalli dried for 15 min were higher than for fullyhydrated thalli. However, emersed photosynthesis of thalli dried for longer than 15 min was lower than fully-hydrated rates and was directly related to percent water loss. Utilizing data from this study, a model was constructed to determine total photosynthetic production of C. peregrina over a single daylight period. From these calculations it was determined that emersed photosynthesis can increase daily photosynthetic production of C. peregrina by 50%.     

The role of metabolic nitrogen in coral calcification

When pieces of the staghorn coral Acropora acuminata are incubated with ¹⁴C-urea, the label is incorporated into skeletal carbonate. Incorporation of this label differs from that of H¹⁴CO ₃ ^- , suggesting urea is not immediately hydrolysed to provide a further source of HCO ₃ ^- . The effects of certain organic substrates upon calcification suggest the ornithine cycle is involved. Citrulline, an ornithine cycle intermediate, is found in high concentrations in the tissues of hermatypic corals. Urea, allantoins, NH₃ and arginine are also present. These compounds are barely detectable in zooxanthellae or an ahermatypic coral. The allantoins may be present as calcium salts. It is suggested that allantoins are the medium by which Ca²⁺ and CO₂ are transported to sites of calcification. Hydrolysis of urea, formed by breakdown of allantoins, yields CO₂ and NH₃. The NH₃ may neutralise protons formed during precipitation of CaCO₃ and bring about their removal from sites of calcification. As well as providing urea, the ornithine cycle may also be involved in the removal of NH₃ from sites of calcification.     

Skeletal calcification patterns in the sea urchin Tripneustes gratilla elatensis (Echinoidea: Regularia)

A comprehensive study on skeletal calcification in the regular echinoid Tripneustes gratilla elatensis was carried out between 1979 and 1981 in the northern Gulf of Eilat (Red Sea), employing size measurement, allometry and radiotracer techniques. Uptake rates of the isotope ⁴⁵Ca were used to estimate the calcification rate of whole tests. Calcification rates of the different skeletal parts and the ⁴⁵Ca uptake along the sutural margins of individual plates were also measured. Whole-test calcification rates for juvenile individuals, 11 to 13 mm in diameter, relative to their skeletal Ca dry weight, calculated using the allometric relationship between skeletal dry weight and diameter, were 1.5 to 1.8% d^-1 for 4 to 8 h of incubation, while calcification rates obtained from periodical size measurements and allometrical constants amounted to 2.75% d^-1. The apparent discrepancy between these results is explained partly by the short duration of the incubations, during which the internal calcium pools, apparently in the coelom, were not fully saturated with the radioactive tracer. This discrepancy decreased when longer radioactive incubations were used, or when a post-incubational deposition of ⁴⁵Ca from these pools was allowed. The size of these pools is roughly 10 mol Ca per 13-mm individual, and it resides probably in the coelom where Ca concentration is 3 times higher than in seawater. The calcification rates given as percentage of skeleton added per day, both for the radioactive and allometric methods, decreased with the urchins' size. The calcification patterns of various components of the skeleton generally fitted their allometrical trends — a relative decrease in the size of the spines, apical plates and lantern. The teeth calcify rapidly to compensate for the constant erosion of their tips. Calcification per plate decreased exponentially from the apex to the peristome. Plate-edge calcification patterns of both interambulacral and ambulacral plates fitted patterns derived from size increment measurements, using natural growth-lines. Typically, most plates grow more horizontally (latitudinally) than vertically. It is suggested that the vertical vs horizontal calcification ratio (v/h) determines the individual plate growth and affects the whole test morphology.     

The mechanism of calcification and its relation to photosynthesis and respiration in the scleractinian coral <Emphasis Type="Italic"> Galaxea fascicularis</Emphasis>

The mechanism of calcification and its relation to photosynthesis and respiration were studied with Ca²⁺, pH and O₂ microsensors using the scleractinian coral Galaxea fascicularis. Gross photosynthesis (Pg), net photosynthesis (Pn) and dark respiration (DR) were measured on the surface of the coral. Light respiration (LR) was calculated from the difference between Pg and Pn. Pg was about seven times higher than Pn; thus, respiration consumes most of the O₂ produced by the algal symbiont's photosynthesis. The respiration rate in light was ca. 12 times higher than in the dark. The coupled Pg and LR caused an intense internal carbon and O₂ cycling. The resultant product of this cycle is metabolic energy (ATP). The measured ATP content was about 35% higher in light-incubated colonies than in dark-incubated ones. Direct measurements of Ca²⁺ and pH were made on the outer surface of the polyp, inside its coelenteron and under the calicoblastic layer. The effects on Ca²⁺ and pH dynamics of switching on and off the light were followed in these three compartments. Ca²⁺ concentrations decreased in light on the surface of the polyp and in the coelenteron. They increased when the light was switched off. The opposite effect was observed under the calicoblastic layer. In light, the level of Ca²⁺ was lower on the polyp surface than in the surrounding seawater, and even lower inside the coelenteron. The concentration of calcium under the calicoblastic layer was about 0.6 mM higher than in the surrounding seawater. Thus Ca²⁺ can diffuse from seawater to the coelenteron, but metabolic energy is needed for its transport across the calicoblastic layer to the skeleton. The pH under the calicoblastic layer was more alkaline compared with the polyp surface and inside the coelenteron. This rise in pH increased the supersaturation of aragonite from 3.2 in the dark to 25 in the light, and brought about more rapid precipitation of CaCO₃. When ruthenium red was added, Ca²⁺ and pH dynamics were inhibited under the calicoblastic layer. Ruthenium red is a specific inhibitor of Ca-ATPase. The results indicated that Ca-ATPase transports Ca²⁺ across the calicoblastic layer to the skeleton in exchange for H⁺. Addition of dichlorophenyldimethylurea completely inhibited photosynthesis. The calcium dynamics under the calicoblastic layer continued; however, the process was less regular. Initial rates were maintained. We conclude that light and not energy generation triggers calcium uptake; however, energy is also needed.     

Seasonal effects of light,temperature, nutrient concentration and salinity on the physiology and growth of Caulerpa paspaloides (Chlorophyceae)

Caulerpa paspaloides (Bory) Greville were collected during the winter and summer (1978 to 1979) from the Florida Keys, USA. Thalli collected during the winter photosynthesized more efficiently at low light intensities (I_c<1, I_k=38 Exm^-2xs^-1) than did thalli collected in the summer (I_c=13, I_k=111 Exm^-2xs^-1). Summer thalli exhibited higher P_max values (2.20 mgO₂xg^-1 dry wtxh^-1) than winter thalli (1.70 mg O₂xg^-1 dry wtxh^-1). Rates of rhizome elongation and frond initiation were strongly inhibited by winter temperatures. The maximum lethal temperature for summer thalli was 37° to 38°C as measured by both growth and photosynthesis. No evidence of nitrogen or phosphorus limitation was found. Relatively minor reductions in salinity (3S) resulted in significant increases in rhizome apex motality. Results indicate that low winter temperatures are responsible for reduced winter growth rates previously reported for the Key Largo population. Increased photosynthetic efficiency at low light intensities and preferential maintenance of rhizome elongation over frond initiation appear to allow this tropical macroalga to optimize growth and survival during the winter.     

Gene flow among population of a teleost (painted greenling,Oxylebius pictus) from Puget Sound to southern California

Net photosynthetic oxygen evolution in Amphiroa anceps (Lamarck) Decaisne is inhibited at high oxygen concentrations. Photosynthesis is highest between pH 6.5 and 7.5. At pH 9 to 10 there is still a significant photosynthetic rate, suggesting that this alga can use HCO _- ³ as a substrate for photosynthesis. At pH 7.0 to 8.5, the photosynthetic rate saturates at a total inorganic carbon concentration (C_i) greater than 3 mM. At pH 8.5 and 8.8, calcification rate continues to increase with increasing concentration of C_i. Between pH 7 and 9, the calcification rate in the light in A. foliacea Lamouroux is proportional to the photosynthetic rate, whereas at higher pH where the photosynthetic rate is very low, the calcification rate is stimulated by the higher concentration of CO _2- ³ ion. At all pH values examined, the calcification rate of living plants in the dark and of dead plants is directly proportional to the CO _2- ³ ion concentration, suggesting little metabolic involvement in calcification processes in the dark, whereas calcification in live A. foliacea in the light is influenced both by the photosynthetic rate and the CO _2- ³ ion concentration in the medium.     

Coral illumination through an optic glass-fiber: incorporation of 14C photosynthates

The pathways of ¹⁴C incorporation into the three major compartments of the coral body were analysed in colonies of Stylophora pistillata. We used the optic glass-fiber method to carry out two sets of experiments: in the first, 11 different colonies were sampled immediately after incubation; in the second, 3 colonies were returned to the reef at the termination of incubation for a further period of 29 h. Within the tissue compartment, significantly more ¹⁴C labeled products were incorporated into illuminated tips or bases than into unilluminated sections. Tips located above illuminated bases contained amounts of ¹⁴C products similar to unilluminated tips. Within the organic matrix compartment, illumination of tip or base segments again resulted in increased amounts of ¹⁴C fixation, and again unilluminated tips located above the illuminated bases did not accumulate more ¹⁴C photosynthates than other tips on the same branches. The absence of detectable translocation was also confirmed after a post-incubation period of 29 h, and raises questions as to the validity of the widely accepted theory of upward translocation. Within the skeletal carbonate compartment, although the results were associated with a high coefficient of variation, significantly more ¹⁴C accumulated in the tips than in the bases. Illumination of tips or bases did not enhance ¹⁴C uptake. A light-independent carbon assimilation (dark fixation) is significant in S. pistillata within the three tested compartments (the tissue, the organic matrix of the skeleton, and the skeletal carbonate). It is suggested that the dark fixation process in corals in a result of accumulation of respiratory CO₂ and CO₂ from sea water as malate or other titratable acids during the night. During the day these acids are broken down, releasing free CO₂ for C₃ pathway photosynthesis.     

Nitrogen fixation by blue-green algae associated with the siphonous green seaweed Codium decorticatum: effects on ammonium uptake

Nitrogen fixation (acetylene reduction) at rates of up to 1.2 g N₂ g dry wt^-1 h^-1 was measured for the siphonous green seaweed Codium decorticatum. No nitrogenase activity was detected in C. isthmocladum. The nitrogenase activity was light sensitive and was inhibited by the addition of DCMU and triphenyl tetrazolium chloride. Additions of glucose did not stimulate nitrogen fixation. Blue-green algae (Calothrix sp., Anabaena sp., and Phormidium sp.) were implicated as the organisms responsible for the nitrogenase activity. They occurred in a reduced microzone within the C. decorticatum thallus where nitrogen fixation was optimized. Nitrogen fixation did not affect the kinetic constants for ammonium uptake in C. decorticatum (K_s=12.0 M, V_max=13.4 mol NH₃ g dry wt^-1 h^-1) determined using the perturbation method. Nevertheless, C. decorticatum thalli which fixed nitrogen had internal dissolved nitrogen concentrations which were over 1.4 times higher than in non-fixing thalli. This suggests that if C. decorticatum does derive part of its nitrogen requirement from the blue-green algae which it harbors, the transfer does not involve competition between this process and the uptake of ambient ammonium.     

Estimation of coral growth-rates from laboratory 45Ca-incorporation rates

Laboratory ⁴⁵Ca-incorporation rates in hermatypic coral skeletons have previously been used successfully as an index of physiological function. This laboratory method would become more meanigful if it also provided an absolute measure of coral growth rates. In two coral species, Porites compressa and Pocillopora damicornis, ⁴⁵Ca incorporation rates were obtained from short (0.5 h) laboratory incubations using apical (determined as fast growing) portions of freshly collected coral branches. ⁴⁵Ca exchange across the coenosarc was not significant and not corrected for, whereas diurnal fluctuation in ⁴⁵Ca in Pocillopora damicornis was significant and a necessary correction. A calculated surface area is used to express calcification rate. Typical growth rates calculated from the ⁴⁵Ca-incorporation rates were 20 and 6 mm/year for Porites compressa and Pocillopora damicornis, respectively. These rates are considerably higher than those previously obtained in the laboratory, and compare favorably with field growth rates — 24 and 14 mm/year, respectively.     

Experimental ecology of the temperate scleractinian coral Astrangia danae I. Partition of respiration,photosynthesis and calcification between host and symbionts

Calcification, photosynthesis and respiration of the scleractinian coral Astrangia danae were calculated from the changes in total alkalinity, pH, calculated total CO₂, and oxygen concentration produced by colonies incubated in glass jars. A correction for changes in ammonia, nitrate and nitrite was taken into account and the method evaluated. The fluxes of oxygen and CO₂ were highly correlated (r=0.99). The statistical error of alkalinity determinations was less than 10% of the changes observed in the slowest calcifying samples. Metabolism of polyparium alone was estimated by difference after removal of tissue and reincubation of bare corallum. Zooxanthellae concentration in the polyps was obtained from cell counts made on homogenates of polyp tissue. The calculated photosynthetic rate of the zooxanthellae in vivo was 25 mol O₂ (10⁸ cell)^-1 h^-1 at a light intensity of 120 Ein m^-2 s^-1. In corals having 0.5x10⁹ zooxanthellae/dm² of colony area up to 8% of the total photosynthesis was attributed to the corallum microcosm. Polyp respiration, photosynthesis, and CaCO₃ uptake rates were all much higher than rates previously reported from A. danae, apparently because in these experiments the organisms were better fed. This increased photosynthesis in turn enhanced calcification still further. The symbiosis therefore appears to provide a growth advantage even to fed corals, under the conditions of these experiments.     

Application of the 45Ca tracer method for determination of calcification rates in calcareous algae: Effect of calcium exchange and differential saturation of algal calcium pools

Calcium exchange and differential saturation of algal calcium pools complicate the application of the ⁴⁵Ca tracer method for the determination of net deposition rates of calcium in calcareous algae. The kinetics of ⁴⁵Ca uptake is critically reevaluated, and it is shown that incorporation occurs in two stages. A fast stage, saturating the exchangeable calcium pools; and a slow stage, giving rise to net deposition. The reliability of the method much depends on the determination of the second rate constant. Calcium net-deposition rates are obtained from the expression , where represents the second rate constant and S _SW the specific activity of the seawater. Calcium exchange and recycling of tracer would lower the second rate constant, hence the method will give rise to minimum values. The application of the method is demonstrated for the following algae: Halimeda incrassata, H. opuntia, Penicillus pyriformis, Udotea flabellum, Cymopolia barbata, Padina sanctae crucis and Amphiroa fragilissima; the results show close agreement of data with independent chemical estimates.Sonderforschungsbereich 95 der Universität Kiel, Publication No. 200.Contribution No. 732 from the Bermuda Biological Station for Research.     

Stable isotope ratio variations in non-scleractinian coelenterate carbonates as a function of temperature

Some coelenterates of the class Hydrozoa and some anthozoan coelenterates from the subclass Octocorallia secrete skeletons of calcium carbonate. Skeletal carbonates of three hydrozoans and of two octocorals were analyzed for the stable isotopes of carbon and oxygen. The results suggest that each of these coelenterates deposits CaCO₃ in oxygen isotopic equilibrium with seawater, and that at least one octocoral, Heliopora, has skeletal carbon in apparent isotopic equilibrium with atmospheric CO₂. Two of these coelenterates, Millepora and Helipora, are significant contributors to the construction of coral reefs. Whereas ¹⁸O of these corals is temperature dependent, ¹³C is not obviously related to temperature. The ¹⁸O-temperature relationship is not significantly different from the oxygen isotope paleotemperature scale developed by Epstein et al. (1953). These findings contrast with numerous analyses of the carbonate in scleractinian coelenterates, which have long been reported to deposit CaCO₃ skeletons whose carbon and oxygen isotopic compositions are not in equilibrium with the external sea-water environment.     

Bestimmung von Redoxzonen in einem mineralölbelasteten Grundwasserleiter

Goal and Scope

The goal of this study is the investigation and the grafic presentation of the characteristic redox zonation in a mineral oil contaminated aquifer which will be formed in the plume downstream of the contamination source. Methanogenic conditions, sulfate-reduction, Fe(III)-reduction, Mn(IV)-reduction, nitrate-reduction, aerobic conditions. By that indications type and degree of microbial degradation which is the most important part in Natural Attenuation (NA) processes can be obtained easily.

Methods

Changes of the groundwater parameters Eh, O₂, NO ₃ ^? , SO₄ ^2?, Fe²⁺, Mn²⁺, HCO₃ ^?, Ca²⁺ will be measured upstream, downstream and also in the centre of the plume. The results will be presented in a sequence of special diagrams.

Results and Conclusion

When microbial degradation of hydrocarbons takes place, a microbial community will always use that electron acceptor from which it will gain a maximum of energy by the corresponding redox-reactions. This means as long as oxygen is available this will be used. After its depletion nitrate serves as electron acceptor leading via nitrite to the formation of nitrogen or ammonia. Manganese (IV) and Iron (III) species which are rather insoluble are mainly available from the soil-phase, can act as electron acceptor as next, leading to soluble Manganese (II) and Iron (II) compounds in groundwater. Finally before methanogenic conditions occur sulphate will become a suitable electron acceptor leading to the formation of hydrogen sulphide. All these processes of mineralization of the hydrocarbons will lead to the production of CO₂ and as consequence to an increase of HCO₃ ^? in groundwater changing the calcareous/carbonic acid-equilibrium. By that more soluble Ca(HCO₃)₂ is formed from insoluble CaCO₃, so the concentration from Ca²⁺ will also inerease. Thus, by the action of microorganisms, a typical redox-zonation and changes of other parameters will occur.

Recommendations and Perspective

To follow the changes in time and space of some characteristic groundwater parameters is a simple way to estimate the potential of microbial degradation in a contaminated aquifer considering Natural Attenuation (NA)-processes.     

Coral calcification: Sources of error in radioisotope techniques

Isotopic exchange occurs between coral skeleton and ⁴⁵Ca⁺⁺ and H¹⁴CO ₃ ^- in seawater. Exchange of ¹⁴C onto skeletons is more rapid than exchange of ⁴⁵Ca⁺⁺. Exchange of ¹⁴C from skeletons to seawater takes place more slowly than exchange of ⁴⁵Ca⁺⁺ to seawater. When living coral is incubated in the dark with radioisotopes for 1 h, the tissues contain considerably more radioactivity than is associated with the skeleton. The tissue radioactivity reflects permeation of tissues and coelenteron by radioactive compounds from the incubation seawater. Addition of alkalis to cardioactive seawater results in a radioactive precipitate, part of which becomes associated with any coral skeleton present, and part of which forms on the wall of the containing vessel. Strong alkali removes biologically-deposited radioisotope from coral skeletons. Deposition, of ¹⁴C from H¹⁴CO ₃ ^- in skeletons of living coral incubated in the dark is greater than in dead coral. The reverse situation occurs with ⁴⁵Ca⁺⁺.     

Some properties of calcium-activated adenosine triphosphatase from the hermatypic coralGalaxea fascicularis

Samples of the hermatypic coralGalaxea fascicularis were collected between April 1987 and April 1990 from coral reefs off Singapore (103 °45E; 1 °13N). Ca²⁺-activated adenosine triphosphatase (ATPase) activity was detected in the plasma-membrane-enriched heavy microsomal fraction ofG. fascicularis. The high affinity component hadKm andVmax values of 0.0021 mM and 0.050 µmol Pi mg^–1 protein min^–1, respectively; corresponding values for the low affinity component were 0.15 mM and 0.85 µmol mg^–1 protein min^–1. The activity of the high affinity component was inhibited 80 and 50%, respectively, by the anticalmodulin drugs calmidazolium and chlorpromazine. The low affinity component of the Ca²⁺-ATPase may represent activities of alkaline phosphatase, Ca²⁺-ATPase from membranes of mitochondria and endoplasmic reticulum, or calmodulin-dissociated plasma membrane Ca²⁺-ATPase resulting from the removal of Ca²⁺ by EDTA during the isolation process. The high affinity Ca²⁺-ATPase is probably the enzyme responsible for Ca²⁺ extrusion from the cells ofG. fascicularis. The high and low affinity components of this Ca²⁺-ATPase could use ATP and ADP as substrates. Maximum activities of both components were registered at pH 7 and at 45°C. Ruthenium red, a specific inhibitor of Ca²⁺-ATPase, inhibited the activities of the high and low affinity Ca²⁺-ATPase by 100 and 60%, respectively. Inhibition of the activities of both components was also observed with sulphydryl reagents (PCMB and mersalyl). However, DCMU, diamox, dinitrophenol, iodoacetate, fluoride, cyanide, ouabain, oligomycin B and L-phenylalanine had no effect on the enzyme activities.     

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.     

Factors affecting the flux of arsenic through the mussel Mytilus galloprovincialis

Radiotracer experiments were designed to study the effects of certain environmental and biological factors on arsenic accumulation and elimination processes in the Mediterranean mussel Mytilus galloprovincialis. Arsenic (as arsenate) uptake increased with increasing arsenic concentration in the water; however, the response was not proportional, indicating that accumulation was partially suppressed at higher external arsenic concentrations. In general, approximately 80% of the ⁷⁴As taken up was associated with the soft parts, with small mussels concentrating ⁷⁴As to a greater degree than larger individuals. The highest ⁷⁴As concentrations were recorded in the byssus and the digestive gland. Increased temperature enhanced both arsenic uptake and loss. Mussels in sea water at 19 S accumulated approximately three times more ⁷⁴As than those held at 38 S. Arsenic loss was much less affected by salinity, with only a tendency for greater arsenic retention noted at lower salinities. Studies carried out in the laboratory and in situ revealed that arsenic turnover was significantly more rapid in actively growing individuals living under natural conditions. Arsenic-74 loss from the in situ group was essentially biphasic, with biological half-times of approximately 3 and 32 days for the fast and slow compartments, respectively. The active secretion of arsenic in the byssal threads contributed to the total elimination of the element from the mussels.