Photosynthetic characteristics of phycoerythrin-containing marine Synechococcus spp.

Marine Synechococcus spp. are sufficiently abundant to make a significant contribution to primary productivity in the ocean. They are characterized by containing high cellular levels of phycoerythrin which is highly fluorescent in vivo. We sought (Jan.–Apr., 1984) to determine the adaptive photosynthetic features of two clonal types of Synechococcus spp., and to provide a reliable physiological basis for interpreting remote sensing data in terms of the biomass and productivity of this group in natural assemblages. It was found that the two major clonal types optimize growth and photosynthesis at low photon flux densities by increasing the numbers of photosynthetic units per cell and by decreasing photosynthetic unit size. The cells of clone WH 7803 exhibited dramatic photoinhibition of photosynthesis and reduction in growth rate at high photon flux densities, accompanied by a large and significant increase in phycoerythrin fluorescence. Maximal photosynthesis of cells grown under 10–50 E m^-2 s^-1 was reduced by 20 to 30% when the cells were exposed to photon flux densities greater than 150 E m^-2 s^-1. However, steady-state levels of photosynthesis maintained for brief periods under these conditions were higher than those of cells grown continuously at high photon flux densities. No photoinhibition occurred in clone WH 8018 and rates of photosynthesis were greater than in WH 7803. Yields of in-vivo phycoerythrin fluorescence under all growth photon flux densities were lower in clone WH 8018 compared to clone WH 7803. Since significant inverse correlations were obtained between phycoerythrin fluorescence and P_max and for both clones grown in laboratory culture, it may be possible to provide a reliable means of assessing the physiological state, photosynthetic capacity and growth rate of Synechococcus spp. in natural assemblages by remote sensing of phycoerythrin fluorescence. Poor correlations between phycoerythrin fluorescene and pigment content indicate that phycoerythrin fluorescence may not accurately estimate Synechococcus spp. biomass based on pigment content alone.     

Photosystem II photoinhibition and altered kinetics of photosynthesis during nutrient-dependent high-light photoadaptation in Gonyaulax polyedra

Gonyaulax poledra Stein was transferred at different cell densities from increasingly nutrient-limited low-light (LL, 80 E m^-2 s^-1) batch-cultures to high-light (HL, 330 E m^-2 s^-1) growth conditions. Several age-dependent differences in HL-adaptation strategies were apparent. Short-term (3h) susceptibility to photosynthetic photoinhibition increased with culture age, with light-limited rates of photosynthesis exhibiting greater photosuppression than light-saturated rates at all stages of growth. These shortterm changes were not accompanied by photobleaching of chlorophyll but were directly related to age-dependent photoinactivation of Photosystem II electron-transport rates. The capacity of electron transport by Photosystem I was only slightly affected. Prolonged exposure of LL log-phase cells to HL conditions did induce photobleaching of chlorophyll associated with increased cell volume, a transient decrease of organic carbon and nitrogen content, enhanced cellular-, carbon-and chlorophyll-based rates of light-saturated photosynthesis (P _max) and suppressed cellular rates of light-limited photosynthesis. As a result, the density of LL log-phase cells doubled and their cellular photosynthetic performance nearly tripled within 1 d of HL exposure while cellular respiratory demands remained unchanged. By contrast, prolonged HL incubation of LL stationary populations induced a transitory burst in cell division and a large reduction in cell volume, leading to a short-term increase in volume-based organic carbon and nitrogen content. Despite reduced cell volume and lowered carbon demand, the cellular-, carbon-and chlorophyll-based rates of P _max in nondividing populations fell by 64, 48 and 27%, respectively, over a 4 d exposure to HL, while light-limited rates were almost fully suppressed within 1 d and chlorophyll a content was reduced by 56%. As a result, the photosynthetic performance of LL-aged cells declined immediately under HL conditions. Addition of inorganic nutrients to LL stationary cultures at the time of HL transfer led to immediate and complete suppression of photosynthesis and cell lysis within 1 d. Addition of nutrients following transfer to HL induced cell responses intermediate to those described for LL log and aged cells exposed to HL. Results support the view that declining nutrient-status impairs HL photoadaptive responses in phytoplankton populations and that the rate and pattern of photoadaptive responses may be used as physiological growth indicators in field studies. The study was conducted from March 1981 to May 1983.     

Photosynthetic characteristics of Prochloron sp./ascidian symbioses

The prokaryotic green alga Prochloron sp. (Prochlorophyta) is found in symbiotic association with colonial didemnid ascidians that inhabit warm tropical waters in a broad range of light environments. We sought to determine the light-adaptation features of this alga in relation to the natural light environments in which the symbioses are found, and to characterize the temperature sensitivity of photosynthesis and respiration of Prochloron sp. in order to assess its physiological role in the productivity and distribution of the symbiosis. Colonies of the host ascidian Lissoclinum patella were collected from exposed and shaded habitats in a shallow lagoon in Palau, West Caroline Islands, during February and March, 1983. Some colonies from the two light habitats were maintained under conditions of high light (2 200 E m^–2 s^–1) and low light (400 E m^–2 s^–1) in running seawater tanks. The environments were characterized in terms of daily light quantum fluxes, daily periods of light-saturated photosynthesis (H_sat), and photon flux density levels. Prochloron sp. cells were isolated from the hosts and examined for their photosynthesis vs irradiance relationships, respiration, pigment content and photosynthetic unit features. In addition, daily P:R ratios, photosynthetic quotients, carbon balances and photosynthetic carbon release were also characterized. It was found that Prochloron sp. cells from low-light colonies possessed lower chlorophyll a/b ratios, larger photosynthetic units sizes based on both reaction I and reaction II, similar numbers of reaction center I and reaction center II per cell, lower respiration levels, and lower P_max values than cells from high-light colonies. Cells isolated from low-light colonies showed photoinhibition of P_max at photon flux densities above 800 E m^–2 s^–1. However, because the host tissue attenuates about 60 to 80% of the incident irradiance, it is unlikely that these cells are normally photoinhibited in hospite. Collectively, the light-adaptation features of Prochloron sp. were more similar to those of eukaryotic algae and vascular plant chloroplasts than to those of cyanobacteria, and the responses were more sensitive to the daily flux of photosynthetic quantum than to photon flux density per se. Calculation of daily minimum carbon balances indicated that, though high-light cells had daily P:R ratios of 1.0 compared to 4.6 for low-light cells, the cells from the two different light environments showed nearly identical daily carbon gains. Cells isolated from high-light colonies released between 15 and 20% of their photosynthetically-fixed carbon, levels sufficient to be important in the nutrition of the host. Q₁₀ responses of photosynthesis and respiration in Prochloron sp. cells exposed briefly (15–45 min) to temperatures between 15° and 45°C revealed a discontinuity in the photosynthetic response at the ambient growth temperatures. The photosynthetic rates were found to be more than twice as sensitive to temperatures below ambient (Q₁₀=3.47) than to temperatures above ambient (Q₁₀=1.47). The Q₁₀ for respiration was constant (Q₁₀=1.66) over the temperature range examined. It appears that the photosynthetic temperature sensitivity of Prochloron sp. may restrict its distribution to warmer tropical waters. The ecological implications of these findings are discussed in relation to published data on other symbiotic systems and free-living algae.     

Photosynthesis and respiration in the alga Ahnfeltia plicata in a flow-through system

Photosynthesis and respiration in Ahnfeltia plicata (Huds.) Fries (Gigartinales) was measured in a seawater flowthrough system at different temperatures, salinities and photon flux densities (PFD). The exchanges of dissolved oxygen and inorganic carbon were continuously recorded with an oxygen probe and a pH electrode measuring variation in CO₂–HCO ₃ ^- equilibrium as pH changes. Highest apparent photosynthesis at moderate photon flux density (PFD 50 E m^-2 s^-1) was found at 15°C and 33 S. Photosynthesis was measured up to PFD 500 E m^-2 s^-1 and no light saturation was documented. In the present experimental set-up, with continuous supply of fresh seawater, the number of limiting factors during photosynthesis measurements is reduced.     

Effects of light intensity on aging of the dinoflagellate Gonyaulax polyedra

Gonyaulax polyedra Stein grown in increasingly nutrientlimited batch culture undergoes the following changes (collectively termed aging): there is a decline in the intracellular concentrations of carbon, nitrogen and photosynthetic pigments; nitrate reductase activity decreases; rates of respiration and photosynthesis fall; and cell division virtually ceases (accompanied in bright light by a decrease in the volume of individual cells). The effect of light intensity on these aging events was tested by growing cells in either bright or dim light. The bright light (330 E m^-2 s^-1) was enough to saturate photosynthesis and the dim light (80 E m^-2 s^-1) was low enough to induce significant shade adaptation of photosynthesis without lowering growth rate. At both light intensities, a decline in carbon and nitrogen content preceded or accompanied all other monitored changes, and the sequence of aging events was similar. However the onset of the decline in intracellular nutrients and photosynthetic rate in low-light cells was delayed by a least one cell division time (i.e., to twice the cell density) in comparison to cells under bright light. At both light levels, pigment-protein complexes of the photosynthetic apparatus began to break down after intracellular carbon and nitrogen had been depleted to a critically low level. The beginning of the drop in pigmentation signalled the end of log-phase growth. It is suggested that the greater pigmentation of low-light cells may represent a larger nutrient supply than found in bright-light cells and could increase the survival time of nutrient-stressed populations.     

Response of Ecklonia radiata (Laminariales) to light at 15°C with reference to the field light budget at Goat Island Bay,New Zealand

Gametophytes of Ecklonia radiata (C.Ag.)J.Ag. grew in culture at 15°C under daily quantum doses ranging from 0.86 to 360 cE m^-2. Growth rates increased with quantum doses up to 40 cE m^-2 d^-1, then reproduction began and the relative growth constant declined while ovum release came earlier with increasing light up to about 100 cE m^-2 d^-1. Above 100 cE m^-2 d^-1 there were no consistent trends with increasing light, except that at the higher quantum doses, fertile female plants had fewer and larger cells and therefore fewer potential ova. Reproduction varied with daily quantum dose rather than with daylength. Given the same daily dose, plants grew fastest in low photon flux density, long daylength conditions. Gametophytes grown in the field developed at similar rates to those in culture. Gametophytes survived seven months of darkness at 10°C but died after one week of darkness at 20° to 23°C. Sunlight of 1 000 E m^-2 s^-1 was fatal to gametophytes and to sporophytes under 2 mm long after 10 to 15 min. Light budgets were prepared for plants growing at 7-and 15-m depths from 1976 to May 1980 in Goat Island Bay, New Zealand (Lat.36° 16S, Long. 174° 48E). Underwater light was measured under various environmental conditions. Relationships between transmission of light through the sea, data from diving visibility records and continuous surface meteorological records were studied. Approximations were made of the average percentage of surface light transmitted to 7 and 15 m over half-monthly periods. By applying these average transmittance values to the records of surface incident light, the average daily quantum doses were calculated. Light on open bottom in Goat Island Bay may sometimes be limiting for gametophyte reproduction in winter at 15-m depth. At depths less than 7 m, summer photon flux densities may reach damaging levels.     

Growth pattern andβ-dimethylsulphoniopropionate (DMSP) content of green macroalgae at different irradiances

Growth rates and intracellular-dimethylsulphoniopropionate (DMSP) concentrations of five green algal species collected from different geographic regions in 1986 and 1989 were determined under four photon flux rates. InUlothrix implexa, U. subflaccida andAcrosiphonia arcta from Antarctica, growth was light-saturated at lower irradiances than in temperateUlva rigida from Southern Chile andBlidingia minima from Germany. The DMSP content ofUlothrix implexa, A. arcta andUlva rigida was directly correlated with the light factor: with increasing irradiance, algal DMSP level increased. In contrast, inUlothrix subflaccida andB. minima DMSP concentrations gradually decreased up to a photon flux rate of 30µmol m^–2 s^–1, then increased markedly under the highest photon flux rate tested. In non-growing, dark-incubatedA. arcta DMSP content was reduced by 35%, while the DMSP pool of all other species remained unchanged, at the level of pre-culture conditions. Under full darkness all plants exhibited a significantly higher DMSP concentration compared with algae grown at low photon flux rates of 2 to 30µmol m^–2 s^–1. These data show a correlation between growth pattern and DMSP biosynthesis, and may point to a species-specific minimum amount of light energy necessary for DMSP accumulation.Contribution no. 302 of the Alfred Wegener Institute of Polar and Marine Research     

Light absorption,photosynthesis and growth of Nannochloris atomus in nutrient-saturated cultures

Nannochloris atomus was maintained in exponential growth at photon flux densities (PFD) from 400 to 700 nm, ranging from 10 to 200 mol m^-2 s^-1. Growth was lightsaturated at PFDs in excess of 100 mol m^-2 s^-1, with a mean light-saturated growth rate at 23 °C of 1.5×10^-5s^-1 (1.2 d^-1). The light-limited growth rates extrapolated to a compensation PFD for growth that was not significantly different from zero, although no changes in cell numbers were observed in a single culture incubated at a PFD of 1.0 mol m^-2s^-1. Dark-respiration rates were independent of PFD, averaging 1.7×10^-6 mol O₂ mol^-1 C s^-1 (0.14 mol O₂ mol^-1 C d^-1). The maximum photon (quantum) efficiency of photosynthesis was also independent of PFD, with a mean value of 0.12 mol O₂ mol^-1 photon. The chlorophyll a-specific light absorption cross-section ranged from 3 to 6×10^-3 m² mg^-1 chl a and was lowest at low PFDs due to intracellular self-shading of pigments associated with high cell-chlorophyll a contents. The C:chl a ratio increased from 10 to 40 mg C mg^-1 chl a between PFDs of 14 and 200 mol m^-2 s^-1. These new observations for N. atomus are compared with our previous observations for the diatom Phaeodactylum tricornutum in terms of an energy budget for microalgal growth.     

Changes in photosynthetic pigment concentration in seaweeds as a function of water depth

We conducted a study of the relationship between changes in photosynthetic pigment content and water depth in Great Harbor near Woods Hole, Massachusetts, USA, on the green algae Ulva lactuca and Codium fragile and the red algae Porphyra umbilicalis and Chondrus crispus. A calibrated underwater photometer equipped with spectral band filters measured light attenuation by the water column. The depth required for a 10-fold diminution of photon flux was 3.6, 5.3, 6.0 and 6.0 m for red, blue, yellow and green light, respectively. Seaweeds were attached to vertically buoyed lines and left to adapt for 7 days; then, with their positions reversed, they were allowed to readapt for 7 days. All species showed greater photosynthetic pigment content with increased depth. Further, the ratio of phycobiliproteins and chlorophyll b to chlorophyll a increased with depth. Changes in pigment content were reversible and occurred in the absence of cell division. There was a net loss of pigments near the surface (high irradiance), and subsequent synthesis when seaweeds were transferred to a position deep in the water column (low irradiance). In contrast, seaweeds which were found in intertidal habitats changed only their pigment concentration, and not pigment ratio, a phenomena analogous to higher plant sun and shade adaptation. Therefore, seaweeds modify their photon-gathering photosynthetic antennae to ambient light fields in the water column by both intensity adaptation and complementary chromatic adaptation.     

Effects of light intensity and nutrient availability on diel patterns of cell metabolism and growth in populations of Synechococcus spp.

Between July 21 and August 8, 1984, phytoplankton were collected from the surface (2 m) and/or chlorophyll maximum of a neritic front, warm-core eddy 84-E and Wilkinson's Basin in the Northwest Atlantic Ocean and incubated up to 38 h in 200-liter vats. Effects of light intensity and nutrient availability on diel patterns of cell metabolism were analyzed in a 0.6- to 1-m fraction, where Synechococcus spp. represented 80 to 100% of the total photoautotrophs. Populations held under in situ conditions exhibited daytime peaks in photosynthetic potential (P_max) that were an order of magnitude higher than nighttime P_max values. Daytime phasing of P_max peaks had no relationship to asynchronous fluctuations in cellular activities of ribulose 1,5 bisphosphate carboxylase (RUBPCase) or phosphoenol pyruvate carboxylase (PEPCase), or to variations in chlorophyll content. Daytime P_max peaks were about 12 h out of phase with nighttime maxima in the frequency of dividing cells (FDC). The phase relationship between P_max and FDC could be altered by manipulating environmental conditions. High light exposure of depp populations did not affect timing of the P_max peak, but its magnitude increased and coincided with increased RUBPCase activity and chlorophyll photobleaching. In the eddy population, a major shift in the timing of peak P_max was induced when increased light intensity was accompanied by nutrient enrichment. This change coincided with major increases in cellular chlorophyll and carboxylating enzyme activity. Lowering irradiance and/or increasing nutrient availability elicited different diel pattern in cellular metabolism in surface populations from the eddy and from Wilkinson's Basin that appeared linked to differences in the nutrient status of the cells. Rates of cell division estimated from the percentage of dividing cells in preserved samples were 0.83 divisions d^-1 in surface warm-core eddy populations, supporting the view that carbon and nitrogen turnover rates in oligotrophic waters can be sufficient to promote near optimal growth of Synechococcus spp.     

Photoadaptation of photosynthesis in Gonyaulax polyedra

Gonyaulax polyedra Stein exhibited a combination of photoadaptive strategies of photosynthesis when only a single environmental variable, the light intensity during growth, was altered. Which of several biochemical/physiological adjustments to the light environment were employed depended on the level of growth irradiance. The photoadaptive strategies employed over any small range of light levels appeared to be those best suited for optimizing photosynthetic performance and not photosynthetic capacity. (Photosynthetic performance, P _i, is defined as the rate of photosynthesis occurring at the level of growth irradiance.) Among all photosynthetic parameters examined, only photosynthetic performance showed a consistent correspondence to growth rates of G. polyedra. Above 3500 to 4000 W cm^-2, where photosynthetic performance was equal to photosynthetic capacity, cells were not considered light-limited in either photosynthesis or growth. At these higher light levels, photosynthetic perfomance, cell volume, growth rates and respiration rates remained maximal; photosynthetic pigment content varied only slightly, while the photosynthetic capacity of the cells declined. At intermediate light levels (3000 to 1500 W cm^-2), photosynthesis, not growth, was light-limited, and photoadaptive strategies were induced which enhance absorption capabilities and energy transfer efficiencies of chlorophyll a to the reaction centers of G. polyedra. Photosynthetic capacity remained constant at about 280 mol O₂ cm^-3 h^-1, while photosynthetic performance ranged from 100 to 130 mol O₂ cm^-3 h^-1. Major increases in photosynthetic pigments, especially peridinin-chlorophyll a-proteins and an unidentified chlorophyll c component, accompanied photoadaptation to low irradiances. Maximal growth rates of 0.3 divisions day^-1 were maintained, as were respiration rates of about-80 mol O₂ cm^-3 h^-1 and cell volumes of about 5.4×10^-8 cm^-3 cell^-1. Below about 1250 W cm^-2, photosynthesis in G. polyedra was so light-limited that photosynthetic performance was unable to support maximal growth rates. Under these conditions, G. polyedra displayed photostress responses rather than photoadaptive strategies. Photostress was manifested as reduced cell volumes, slower growth, and drastic reductions in pigmentation, photosynthetic capacity, and rates of dark respiration.     

A comparative study of photoadaptation in four diatoms isolated as endosymbionts from larger foraminifera

Four endosymbiotic diatoms were isolated from 2 species of larger foraminifera collected in the Red Sea and Hawaii. The photoadaptive responses of the cultured diatoms were measured at 312, 19 and 7 W cm^-2. Two of the diatoms (Fragilaria shiloi and Nitzschia laevis), both isolated from Amphistegina lessonii, grew fastest at 312 W cm^-2. The other two diatoms (N. valdestriata and N. panduriformis) which were isolated from Heterostegina depressa, grew best at 19 W cm^-2. Of the four diatoms, F. shiloi grew best at high light levels. Also in F. shiloi, chlorophyll c content per cell was directly proportional to light intensity; in contrast chlorophyll a and carotenoids increased to maxima at 19 W cm^-2. The chlorophyll a and c and carotenoid content of N. valdestriata were also maximal at 19 W cm^-2. Photosynthetic rates, measured by respirometry, suggested that the diatoms were photoinhibited at higher light intensities and did well at moderately low light intensities (175W cm^-2). The photocompensation points of all 4 diatoms were about 2% of the light available in the spring at 1-m depth at Elat on the Red Sea. At Elat the photocompensation point would lie between 40 and 50 m if the algae were free in nature. The amount of attenuation of light by the shells of the host has not yet been measured. Presumably photocompensation of the algae within hosts is reached at depths less than 40 m.     

Dynamics and physiology of saxitoxin production by the dinoflagellatesAlexandrium spp.

Toxin content (fmol cell^–1) and a suite of elemental and macromolecular variables were measured in batch cultures of the dinoflagellatesAlexandrium fundyense, A. tamarense andAlexandrium sp. from the southern New England region, USA. A different perspective was provided by semicontinuous cultures which revealed sustained, steady-state physiological adaptations by cells to N and P limitation. Two types of variability were investigated. In batch culture, changes in nutrient availability with time caused growth stage variability in toxin content, which often peaked in mid-exponential growth. A second type of variability that could be superimposed on growth stage differences is best exemplified by the high toxin content of cells grown at suboptimal temperatures. Calculations of the net rate of toxin production (R _tox ; fmol cell^–1 d^–1) for these different culture treatments and modes made it possible to separate the dynamics of toxin production from cell division. Over a wide range of growth rates, cells produced toxin at rates approximating those needed to replace losses to daughter cells during division. The exception to this direct proportionality was with P limitation, which was associated with a dramatic increase in the rate of toxin production as cells stopped dividing due to nutrient limitation in batch culture. Growth stage variability in batch culture thus reflects small imbalances (generally within a factor of two) between the specific rates of toxin production and cell division. N limitation and CO₂ depletion both affect pathways involved in toxin synthesis before those needed for cell division; P limitation does the opposite. The patterns of toxin accumulation were the same as for major cellular metabolites or elemental pools. The highest rates of toxin production appear to result from an increased availability of arginine (Arg) within the cell, due to either a lack of competition for this amino acid from pathways involved in cell division or to increased de novo synthesis. There were no significant changes in toxin content with either acclimated growth at elevated salinity, or with short term increases or decreases of salinity. These results demonstrate that toxin production is a complex process which, under some conditions, is closely coupled to growth rate; under other conditions, these processes are completely uncoupled. Explanations for the observed variability probably relate to pool sizes of important metabolites and to the differential response of key biochemical reactions to these pool sizes and to environmental conditions.     

Ecotypic differentiation in the marine diatom Skeletonema costatum: influence of light intensity on the photosynthetic apparatus

Three genetically distinct clones of Skeletonema costatum (Grev.) Cleve were grown at 20°C under high (274 E m^-2 s^-1) and low (27 E m^-2 s^-1) light conditions and their photoadaptive photosynthetic responses compared. When all three clones were grown under low light, pigment analyses and fluorescence excitation spectra demonstrated that the accessory pigments, chlorophyll c and fucoxanthin, became more important in light-harvesting compared to chlorophyll a. Photosynthetic unit sizes increased for Photosystems I and II in low light, but photosynthesis vs irradiance characteristics were not reliable predictors of photosynthetic unit features. Fluorescence excitation spectra and photosynthesis vs irradiance (P-I) relationships indicated that changes in energy transfer occurred independent of changes in pigment content. Large increases in accessory pigment content were not accompanied by large increases in excitation from these pigments. Changes in energy transfer properties were as important as changes in PSU size in governing the photoadaptive responses of S. costatum. When the three clones were grown under identical conditions, each had a separate and distinct pattern of photoadaptation. Significant differences among clones were found for pigment ratios, photosynthetic unit sizes for Photosystems I and II and efficiency of energy transfer between pigments. These strikingly different photoadaptive strategies among clones may partially account for the great ecological success of the diatom species. This is the first quantitative investigation of the importance of both chlorophyll c and fucoxanthin to the adaptive responses of diatoms to light intensity, and represents the most complete characterization of the photoadaptive responses of a single species of marine phytoplankter to differences in light environment.     

Autecology and clonal variability of the marine centric diatom Thalassiosira rotula (Bacillariophyceae) in response to light,temperature and salinity

The influence of 49 combinations of salinity (10–40 S, at 5 S intervals) and temperature (0°–30°C, at 5C° intervals) on the maximum daily division rate (K) and 18 combinations of light intensity (six levels) and temperature (5°, 15°, and 25°C) on photosynthesis, cell division, and chlorophyll a was examined using two clones of Thalassiosira rotula Meunier isolated from the upwelling area of Baja California (clone C8) and from Narragansett Bay, Rhode Islands (clone A8). Physiological differences appear to characterize these to clones with regard to their temperature tolerance (C8 5°–30°C, A8 0°–25°C), maximum growth rate (C8 K=2.9, A8 K=2.4), chlorophyll a content, and in the rates of growth and photosynthesis in response to light intensity and temperature. Optimum salinity for both clones (25–30 S) was generally independent of temperature, while chlorophyll a content decreased with temperature. T. rotula is a cosmopolitan paractic species; experimental studies indicate that it is eurythermal and moderately euryhaline. Comparison of five additional Narragansett Bay isolates of T. rotula reveal minimal spacial or temporal variability in genetically determined physiological characteristics within this local population.     

Contribution ofSynechococcus spp. to size-fractioned primary productivity in three water masses in the Northwest Atlantic Ocean

The distribution of phycoerythrin-richSynechococcus spp. relative to eukaryotic algae and the contribution ofSynechococcus spp. toin situ primary production were compared at a neritic front, in warm-core eddy 84-E, and at Wilkinson's Basin, during a cruise to the Northwest Atlantic Ocean in July/August 1984. Immunofluorescence analyses ofSynechococcus strains demonstrated the restricted distribution of the tropical oceanic serogroup to the warm-core eddy, while strains of the neritic serogroup and those labelled by antiserum directed against a motile strain, were abundant in all three water masses. Although the majority ofSynechococcus spp. cells were observed in the 0.6 to 1 m fraction, an increasing proportion of the totalSynechococcus spp. cells were found in the 1 to 5 m fraction as nitrate concentrations increased near the base of the thermocline. From immunofluorescence analyses, we determined that the increasing proportion of largerSynechococcus spp. cells at depth was not the result of a change in strain composition, and may therefore be associated with increasing cell volume due to the enhanced nutrient supply. The contribution of the different size fractions to the total standing crop of chlorophyll and thein situ rate of photosynthesis was distincty different for the three water masses. At the neritic front, the larger photoautotrophs of the 1 to 5 m and >5 m fractions were the major contributors to chlorophyll concentrations and primary production.Synechococcus spp. appeared to provide only 6% of the dawn-to-duskin situ primary production at the neritic front. In modified Sargasso water in the warm-core eddy,Synechococcus spp. contributed 25% to thein situ rate of integrated primary production. In this warm-core eddy, the 0.2 to 0.6 m fraction made a major contribution to the standing crop of chlorophyll and primary production that equalled or exceeded that of the larger sze categories. Furthermore, at the bottom of the euphotic layer, eukaryotes numerically dominated the 0.2 to 0.6 m fraction, which contributed 61% of the primary productivity. At Wilkinson's Basin, theSynechococcus spp.-dominated 0.6 to 1.0 m fraction made the greatest contribution to the standing crop of chlorophyll an primary production, while smaller photoautotrophs (0.2 to 0.6 m) accounted for little of the chlorophyll or photosynthetic rates measured over the euphotic layer. Largest numbers ofSynechococcus spp. (2.9x10⁸ cells l^-1) occurred at the 18% isolume, coincident with a shoulder in the chlorophyll fluorescence profile and the site of maximumin situ primary productivity. At Wilkinson's Basin,Synechococcus spp. contributed 46% to thein situ photosynthesis integrated over the water-column.     

Photosynthetic and optical properties of the marine chlorophyte Dunaliella tertiolecta grown under fluctuating light caused by surface-wave focusing

Photosynthetic and optical properties of the marine chlorophyte Dunaliella tertiolecta Butcher were studied in response to irradiance fluctuations caused by surface-wave focusing. The experimental conditions simulated the prominent features of the light field (high average irradiance, spectral composition and statistical properties) in the uppermost few meters of the water column under sunny surface conditions. The properties of algae grown under high-frequency fluctuations were compared with control cells grown under constant light at the same average irradiance (800 mol quantam^-2s^-1). No significant differences were found for a number of parameters, including growth rate, cellular chlorophyll a and pigment ratios, photosynthetic unit size and density of Photosystem I reaction centers, the rate of photosynthesis at the growth irradiance, dark respiration, and in vivo fluorescence of chlorophyll a per cell. Photosynthetic parameters were not affected by whether the incident light for oxygen exchange measurements was fluctuating or constant. This was the case whether the cells had been previously acclimated to either fluctuating or constant irradiance. Such a photosynthetic response indicates that cells are accomplishing a time integration of the fluctuating light. In addition, although D. tertiolecta is capable of dramatically changing its optical properties in response to low or high growth irradiance levels, the refractive index of the cells, the efficiency factors for light absorption and scattering by individual cells, and chlorophyll-specific absorption and scattering coefficients of cell suspensions, were all very similar under high irradiance, whether or not wave focusing was present.Contribution to the program of GIROQ (Groupe Interuniversitaire de Recherches Océanographiques du Québec)     

Chlorophyll a fluorescence in marine centric diatoms: Responses of chloroplasts to light and nutrient stress

Observations at sea of large variations in the cellular fluorescence of phytoplankton prompted a study of the fluorescence responses in marine diatoms to light and nutrient stress. When older cultures of Lauderia borealis were exposed to intense light, the in vivo fluorescence of chlorophyll a declined within the first 2 min of exposure. This initial response to light stress appeared to be correlated with a contraction of the chloroplasts. Continued exposure led to a second decline in fluorescence, which required 30 to 60 min for completion. A movement of chloroplasts to the valvar ends of the cell caused this secondary response. Both the contraction and intracellular movement of chloroplasts appeared to be related to both photoinhibition of photosynthesis and diel fluctuations in cellular fluorescence. An investigation of continuous cultures of Cyclotella nana showed that in vivo chlorophyll a fluoresced more strongly in nitrogen-starved cells than in enriched ones. Photoinhibition of cellular fluorescence also increased with the cell's state of nitrogen deficiency.     

Implications of salinity fluctuation for growth and nitrogen metabolism of the marine diatom Ditylum brightwellii in comparison with Skeletonema costatum

In 1987 effects of salinity fluctuations on growth of Ditylum brightwellii (West) Grunow, isolated from the Eastern Scheldt estuary (SW Netherlands) in 1981, were studied. D. brightwellii was grown in a 12 h light: dark cycle at constant salinity in brackish media. Ammonium-limited cultures were subjected to a salinity fluctuation. By decreasing the salinity to 4.8 photosynthesis and cell division were inhibited; cells were deformed. Protein and carbohydrate contents increased slightly, dark respiration was stimulated and cellular levels of glucose decreased at low salinity; this indicated a possible role of sugars in osmoregulation. Ammonium was accumulated in cultures, amino acids may have been stored; the role of the vacuole as a storage compartment was discussed. Both the ammonium uptake capacity and the affinity for ammonium decreased. Nitrogen limitation was relieved in the transient state. [With the activity of the nitrogen assimilation enzymes glutamine synthetase (GS) and glutamate synthase (GOGAT) being uninhibited by lower salinity.] Recovery from hypo-osmotic stress during a salinity increase was initiated by stimulated photosynthesis; chlorophyll a increased, but persistant contractions of cytoplasm (with chloroplasts) may have delayed cell growth. The glutamate dehydrogenase (GDH) activity decreased further whereas the cellular level of alanine increased in the presence of large ammonium pools; this may indicate a temporary activity of ADH (alanine dehydrogenase). Skeletonema costatum (Greville) Cleve, recovered faster from hypoosmotic stress than did D. brightwellii. Due to an osmotic shock from 13.6 to 7.1 S both species excreted amino acids and glucose; S. costatum accumulated more glucose, D. brightwellii accumulated more amino acids. S. costatum may with the competition for nitrogen in waters with an unstable salinity; it will replace D. brightwellii.Contribution no. 427 Delta Institute for Hydrobiological Research, Yerseke, The Netherlands     

Adaptation of solitary corals and their zooxanthellae to low light and UV radiation

Adaptation of solitary corals, Fungia repanda and F. echinata, and their zooxanthellae to low light and ultraviolet light B (UV-B) was studied with respect to changes in their protein contents, photosynthetic pigment contents and the photosynthesis-irradiance (P-I) curves. The corals were collected from 1 to 50 m depths in the Republic of Belau (Paulau) in 1990 and 1991. The chlorophyll a content in a unit surface area of the coral did not change significantly with the depth of the habitat, whereas cellular chlorophyll a in the algae increased with the depth. Zooxanthellae density and protein content in a unit surface area of Fungia spp. decreased with the depth. Photosynthetic parameters normalized by a unit surface area of the Fungia spp., maximum gross photosynthetic rate (P _gmax area^-1) and dark respiration rate (R area^-1), were negatively correlated with the depth, while initial slope of the P-I curve () did not show significant correlation with the depth. Compensation light intensity (Ic) decreased with the depth. In isolated zooxanthellae, P _max chl a ^-1, and R chl a ^-1 decreased with the depth, while _{chl a} was constant. P _gmax cell^-1 and R cell^-1 did not change significantly but _cell increased with the depth. Ic decreased with the depth as in the intact corals. Reduction of protein content in a unit area of the coral from deeper habitat implies decrease of host animal tissues. Reduction of Ic can be explained by decrease of R area^-1, which may be due to the diminution of animal tissues. The photoadaptational response to low light intensity of intact Fungia spp. was found to be a combination of the photoadaptation of symbiotic algae and the decrease of host animal tissue. In order to study their adaptation to ultraviolet (UV) radiation, P-I curves of Fungia spp. and isolated zooxanthellae were analyzed before and after UV-B irradiation. 1 h UV-B irradiation showed no effect on the photosynthetic rate of the shallow water (1 m) corals, while it inhibited the photosynthesis of the deep water (30 m) corals and zooxanthellae isolated from both shallow and deep water corals. These results indicate that the host, Fungia spp., in shallow water have protective mechanism for intense UV-B in their habitat. These photoadaptational mechanisms seem to allow the Fungia spp. to have wide vertical distribution where light intensity spans more than two orders of magnitude.