LIGHT AND TEMPERATURE AS FACTORS REGULATING SEASONAL GROWTH AND DISTRIBUTION OF ULOTHRIX ZONATA (ULVOPHYCEAE)1

Ulothrix zonata (Weber and Mohr) Kütz. is an unbranched filamentous green alga found in rocky littoral areas of many northern lakes. Field observations of its seasonal and spatial distribution indicated that it should have a low temperature and a high irradiance optimum for net photosynthesis, and at temperatures above 10°C it should show an increasingly unfavorable energy balance. Measurements of net photosynthesis and respiration were made at 56 combinations of light and temperature. Optimum conditions were 5°C and 1100 μE·m^?2·s^?1 at which net photosynthesis was 16.8 mg O₂·g^?1·h^?1. As temperature increased above 5° C optimum irradiance decreased to 125 μE·m^?2·s^?1 at 30°C. Respiration rates increased with both temperature and prior irradiance. Light-enhanced respiration rates were significantly greater than dark respiration rates following irradiance exposures of 125 μE·m^?2·s^?1 or greater. Polynomials were fitted to the data to generate response surfaces. Polynomial equations represent statistical models which can accurately predict photosynthesis and respiration for inclusion in ecosystem models.     

Modulation of osmotic stress effects on photosynthesis and respiration by temperature in mesophyll protoplast of pea

Exposure of mesophyll protoplast of pea to osmotic stress decreases the rate of photosynthesis while stimulating marginally the respiratory rate of mesophyll protoplasts. The interaction of osmotic and temperature stress during the modulation of photosynthetic and respiratory rates of pea (Pisum sativum var Azad P1) mesophyll protoplasts was investigated. The protoplasts were exposed to either iso-osmotic (0.4 M) or hyper-osmotic (1.0 M) concentration of sorbitol at 15 degrees and 25 degrees C. The rates of photosynthesis and respiration were studied. At optimum temperature of 25 degrees C, there was a decrease in photosynthesis (< 10%) at hyper-osmoticum (osmotic effect), whereas respiration increased marginally (by about 15%). Low temperature (15 degrees C) aggravated the sensitivity of both respiration and photosynthesis to osmotic stress. At 15 degrees C, the decrease in photosynthesis due to osmotic stress was > 35%, while the respiratory rate was stimulated by 30%. The relative proportion of cytochrome pathway decreased by about 50% at both 15 degrees C and 25 degrees C while that of alternative pathway increased, more so, at 15 degrees C, when the mesophyll protoplasts were subjected to hyper-osmoticum stress. The titration experiments showed that extent of engagement of alternative pathway was higher, the slope value was slightly higher for 15 degrees C compared to 25 degrees C. Low temperature modulates the effect of hyper-osmoticum stress on photosynthesis and respiration, and results in increased participation of alternative pathway.     

Gas exchange characteristics of Gulf of Mexico coastal marsh macrophytes

Gas exchange characteristics of three major Louisiana Mississippi River deltaic plain marsh species, Spartina patens (Ait.) Muhl., Spartina altemiflora Lois., and Panicum hemitomon Shult., was studied under controlled environment conditions. The optimum temperature for maximum photosynthesis was ≈ 36 °C for S. patens, 27 °C for S. alterniflora, and 28 °C for rP. hemitomon. Net photosynthesis rates at optimum temperature averaged 20.1 μmol · m^t-2 · s^t-1 in S. patens, 22.8 μmol · m⁻² · s⁻¹ in S. alterniflora, and 11.4 μmol · m⁻² · s⁻¹ in P. hemitomon. Photosynthetic light saturation occurred ≈720, 530, and 750 μmol · m⁻² · s⁻¹ in S. patens, S. alterniflora, and P. hemitomon, respectively. Only S. patens had a midday depression of stomatal conductance, but net photosynthesis was not reduced by the depression. Maximum stomatal conductances were 285 mmol · m⁻² · s⁻¹ in S. patens, 238 mmol · m⁻² · s⁻¹ in S. alterniflora, and 335 mmol · m⁻² · s⁻¹ in P. hemitomon. In contract, net photosynthesis values were lower in P. hemitomon compared with the Spartina species, indicating a greater degree of water use efficiency of photosynthesis for both Spartina species.     

Influence of light and temperature on photosynthesis and respiration by Pithophora oedogonia (Mont.) Wittr. (chlorophyceae)

Rates of net photosynthesis and respiration were determined for Pithophora oedogonia (Mont.) Wittr. acclimatized to 56 combinations of light (7–1200 μE m^?2 s^?1) and temperature (5–35°C). Conditions for maximum net photosynthesis were estimated to be 26°C and 970 μE m^?2 s^?1. The rate of net photosyntheses varied considerably with temperature, with the maximum measured value (9.67 mg O₂ h^?1 g dry wt.^?1) occurring at 25°C. Respiration rate increased with temperature and the light received just prior to measurement. The maximum respiration rate (7.05 mg O₂ g^?1 h^?1) occurred at 30°C and 1200 μE m^?2 s^?1. Exposure of Pithophora to light levels of 600 or 1200 μE m^?2 s^?1 prior to determination of the respiration rate resulted in significantly elevated levels of oxygen consumption at temperatures ≥ 15°C. The relationship between light, temperature and photosynthesis and respiration were summarized as three-dimensional response surfaces.     

Photosynthesis and respiration in bladelets of Ecklonia cava Kjellman (Laminariales, Phaeophyta) in two localities with different temperature conditions

Characteristics of photosynthesis and respiration of bladelets were compared between Ecklonia cava Kjellman sporophytes growing in a warmer temperate locality (Tei, Kochi Pref., southern Japan) and in a cooler temperate locality (Nabeta, Shizuoka Pref., central Japan). Photosynthesis and respiration were measured with a differential gas-volumeter (Productmeter). In photosynthesis-light curves at 20°C, the rate of net photosynthesis was almost the same at light intensities lower than 25 μmol m⁻² s⁻¹ and the light-saturation occurred at 200–400 μmol m⁻²s⁻¹ in plants of both localities. The light-saturated net photosynthetic rates were higher in winter and spring than in summer and autumn in both plants. The optimum temperature for net photosynthesis at 400 μmol m⁻²s⁻¹ was 27°C throughout the year in the Tei plant and 25–27°C in the Nabeta plant. The decrease of net photosynthetic rates in the supraoptimal temperature range up to 29°C was sharper in winter and spring than in summer and autumn in both plants, being smaller in the Tei plant than in the Nabeta plant in all seasons. The dark respiration rate always increased with water temperature rise in both plants. No clear differences were found in the dark respiration rate between Tei and Nabeta plants except that when measured against dry weight, the Tei plant showed a slightly lower rate as compared with the Nabeta plant.     

PRODUCTIVITY OF THE FILAMENTOUS ALGA PITHOPHORA OEDOGONIA (CHLOROPHYTA) IN SURREY LAKE,INDIANA1

Biomass, akinete numbers, net photosynthesis, and respiration of Pithophora oedogonia were monitored over two growing seasons in shallow Surrey Lake, Indiana. Low rates of photosynthesis occurred from late fall to early spring and increased to maximum levels in late spring to summer (29–39 mgO₂·g^?1 dry wt·h^?1). Areal biomass increased following the rise in photosynthesis and peaked in autumn (163–206g dry wt·m^?2). Photosynthetic rates were directly correlated with temperature, nitrogen, and phosphorus over the entire annual cycle and during the growing season. Differences in photosynthetic activity and biomass between the two growing seasons (1980 and 1981) were apparently related to higher, early spring temperatures and higher levels of NO₃-N and PO₄-P in 1981. Laboratory investigations of temperature and light effects on Pithophora photosynthesis and respiration indicated that these processes were severely inhibited below 15°C. The highest P_max value occurred at 35°C (0.602 μmol O₂·mg^?1 chl a·min^?1). Rates of dark respiration did not increase above 25°C thus contributing to a favorable balance of photosynthetic production to respiratory utilization at high temperatures. Light was most efficiently utilized at 15°C as indicated by minimum values of I_k(47 μE·m^?2·s^?1) and I_c (6 μE·m^?2·s^?1). Comparison of P. oedogonia and Cladophora glomerata indicated that the former was more tolerant of temperatures above 30°C. Pithophora's tolerance of high temperature and efficient use of low light intensity appear to be adaptive to conditions found within the dense, floating algal mats and the shallow littoral areas inhabited by this filamentous alga.     

Primary production of phytoplankton in Lake Valencia (Venezuela)

Lake Valencia is heavily polluted by waste water of domestic, agricultural and industrial origin. The high organic load may have produced important changes in the limnological properties. Cyanobacteria dominated in numbers and biomass (over 90% throughout the year). Chlorophyll-a content averaged 37.7 + 15 μg · 1⁻¹. Maximum concentrations of 50–80 μg · 1⁻¹ were found near the inflows affected by organically polluted affluents. There has been a 50% reduction in the euphotic zone in only 13 years. The maximum rate of gross photosynthesis per hour at light saturation was determined within the uppermost 1-meter layer. The highest value was 16,290 mg O₂ · m⁻³ · h⁻¹. Lake Valencia is among the most productive lakes in the world, with areal net photosynthesis averaging 7.5 g C · m⁻² · d⁻¹.     

Photosynthetic characteristics of the shade-adapted C4 grass Muhlenbergia sobolifera (Muhl.) Trin.: control of development of photorespiration by growth temperature

Muhlenbergia sobolifera (Muhl.) Trin., a C₄ grass, occurs in understory habitats in the northeastern United States. Plants of M. sobolifera were grown at 23 and 30°C at 150 and 700 μmol photons m⁻² s⁻¹. The photosynthetic CO₂ compensation point, maximum CO₂ assimilation, dark respiration and the absorbed quantum use efficiency (QUE) were measured at 23 and 30°C at 2 and 20% O₂. Photosynthetic CO₂ compensation points ranged from 4 to 14mm³ dm⁻³ CO₂ and showed limited O₂ sensitivity. The mean photosynthetic CO₂ compensation point of plants grown at 30°C (4·5 mm³ dm⁻³) was 57% lower and 80% less inhibited by O₂ than that of plants grown at 23°C. Photosynthesis was similarly affected by growth temperature, with 70% more O₂ inhibition in plants grown at 23°C; suppression over all treatments ranging from 2 to 11%. Unlike typical C₄ species, plants of M. sobolifera from both temperature regimes exhibited higher CO₂ assimilation rates when grown at low light. Growth temperature and light also affected QUE; plants grown at low light and 23°C had the highest value (0·068 mol CO₂/mol quanta). Measurement temperature and growth light regime significantly affected dark respiration; however, O² did not affect QUE or dark respiration under any growth or measurement conditions. The results indicate that M. sobolifera is adapted to low PPFD, and that complete suppression of photorespiration is dependent upon high growth temperature.     

Osmotic adjustment by intact isolated chloroplasts in response to osmotic stress and its effect on photosynthesis and chloroplast volume

Spinach leaf chloroplasts isolated in isotonic media (330 millimolar sorbitol, −1.0 megapascals osmotic potential) had optimum rates of photosynthesis when assayed at −1.0 megapascals. When chloroplasts were isolated in hypertonic media (720 millimolar sorbitol, −2.0 megapascals osmotic potential) the optimum osmotic potential for photosynthesis was shifted to −1.8 megapascals and the chloroplasts had higher rates of CO₂-dependent O₂ evolution than chloroplasts isolated in 330 millimolar sorbitol when both were assayed at high solute concentrations.

Transfer of chloroplasts isolated in 330 millimolar sorbitol to 720 millimolar sorbitol resulted in decreased chloroplast volume but this shrinkage was only transient and the chloroplasts subsequently swelled so that within 2 to 3 minutes at 20°C the chloroplast volume had returned to near the original value. Thus, actual steady state chloroplast volume was not decreased in hypertonic media. In isotonic media, there was a slow but significant uptake of sorbitol by chloroplasts (10 to 20 micromoles per milligram chlorophyll per hour at 20°C). Transfer of chloroplasts from 330 millimolar sorbitol to 720 millimolar sorbitol resulted in rapid uptake of sorbitol (up to 280 micromoles per milligram chlorophyll per hour at 20°C) and after 5 minutes the concentration of sorbitol inside the chloroplasts exceeded 500 millimolar. This uptake of sorbitol resulted in a significant underestimation of chloroplast volume unless [¹⁴C]sorbitol was added just prior to centrifuging the chloroplasts through silicone oil. Sudden exposure to osmotic stress apparently induced a transient change in the permeability of the chloroplast envelope since addition of [¹⁴C]sorbitol 3 minutes after transfer to hypertonic media (when chloroplast volume had returned to normal) did not result in rapid uptake of labeled sorbitol.

It is concluded that chloroplasts can osmotically adjust in vitro by uptake of solutes which do not normally penetrate the chloroplast envelope, resulting in a restoration of normal chloroplast volume and partially preventing the inhibition of photosynthesis by high solute concentrations. The results indicate the importance of matching the osmotic potential of isolation media to that of the tissue, particularly in studies of stress physiology.

     

Carbon balance of Yucca elata Engelm. during a hot and cool period in situ

Respiratory activity of intact, attached roots was measured under field and controlled conditions. Root respiration of Yucca elata Engelm. was highly temperature dependent: Q₁₀ values decreased from 2.1 (12–22° C) to 1.7 (26–36° C) as temperatures increased. Respiration ceased after 5 h at 42° C. In the field, in August, when net leaf photosynthesis was severely depressed, the diel fluctuation in the respiration rate of suberized and partially suberized roots was predominantly a function of temperature. A photoperiod-associated rise in respiration rates apart from temperature response occurred in February for nonsuberized, partially suberized, and suberized roots when active net photosynthesis occurred throughout the photoperiod. In whole-plant root systems, respiratory CO₂ was 3.2 and 4.3 mg CO₂·g DW^-1·d^-1 in August and February, respectively, when adjusted for the proportion of suberized and nonsuberized lateral roots. On a whole-plant basis, 0.89 mg C·g DW^-1·d^-1 was gained during February and 0.46 mg C·g DW^-1·d^-1 was lost in August. The belowground: aboveground ratio of whole-plants in situ was 0.42 on a shallow soil where vertical root growth was limited to a soil depth of 68 cm and ranged from 1.29 to 5.94 \(\left( {\bar x = 3.31} \right)\) in deep sands. No leaf dark fixation of CO₂ was observed in field plants during August and February, nor in well-watered plants or plants subjected to drought in laboratory studies. Although small diel fluctuations in leaf acidity occurred in both field and greenhouse-grown plants, results of this study suggest that Y. elata is a C₃ plant.     

PHYSIOLOGICAL RESPONSES OF ANABAENA VARIABILIS (CYANOPHYCEAE) TO INSTANTANEOUS EXPOSURE TO VARIOUS COMBINATIONS OF LIGHT INTENSITY AND TEMPERATURE1

Light intensity and temperature interactions have a complex effect on the physiological process rates of the filamentous bluegreen alga Anabaena variabilis Kütz. The optimum temperature for photosynthesis increased with increasing light intensity from 10°C at 42 μE·m^?2·s^?1 to 35°C at 562 μE·m^?2·s^?1. The light saturation parameter, I_K, increased with increasing temperatures. The maximum photosynthetic rate (2.0 g C·g dry wt.^?1·d^?1) occurred at 35°C and 564 μE·m^?2·s^?1. At 15°C, the maximum rate was 1.25 g C·g dry wt.^?1·d^?1 at 332 μE·m^?2·s^?1. The dark respiration rate increased exponentially with temperature. Under favorable conditions of light intensity and temperature the percent of extracellular release of dissolved organic carbon was less than 5% of the total C fixed. This release increased to nearly 40% under combinations of low light intensity and high temperature. A mathematical model was developed to simulate the interaction of light intensity and temperature on photosynthetic rate. The interactive effects were represented by making the light-saturation parameters a function of temperature.     

PHOTOSYNTHESIS AND RESPIRATION OF THE CONCHOCELIS STAGE OF ALASKAN PORPHYRA (BANGIALES,RHODOPHYTA) SPECIES IN RESPONSE TO ENVIRONMENTAL VARIABLES1

Photosynthesis and respiration of three Alaskan Porphyra species, P. abbottiae V. Krishnam., P. pseudolinearis Ueda species complex (identified as P. “pseudolinearis” below), and P. torta V. Krishnam., were investigated under a range of environmental parameters. Photosynthesis versus irradiance (P–I) curves revealed that maximal photosynthesis (P_max), irradiance at maximal photosynthesis (I_max), and compensation irradiance (I_c) varied with salinity, temperature, and species. The P_max of Porphyra abbottiae conchocelis varied between 83 and 240 μmol O₂ · g dwt^?1 · h^?1 (where dwt indicates dry weight) at 30–140 μmol photons · m^?2 · s^?1 (I_max) depending on temperature. Higher irradiances resulted in photoinhibition. Maximal photosynthesis of the conchocelis of P. abbottiae occurred at 11°C, 60 μmol photons · m^?2·s^?1, and 30 psu (practical salinity units). The conchocelis of P. “pseudolinearis” and P. torta had similar P_max values but higher I_max values than those of P. abbottiae. The P_max of P. “pseudolinearis” conchocelis was 200–240 μmol O₂ · g dwt^?1 · h^?1 and for P. torta was 90–240 μmol O₂ · g dwt^?1 · h^?1. Maximal photosynthesis for P. “pseudolinearis” occurred at 7°C and 250 μmol photons · m^?2 · s^?1 at 30 psu, but P_max did not change much with temperature. Maximal photosynthesis for P. torta occurred at 15°C, 200 μmol photons · m^?2 · s^?1, and 30 psu. Photosynthesis rates for all species declined at salinities <25 or >35 psu. Estimated compensation irradiances (I_c) were relatively low (3–5 μmol · photons · m^?2 · s^?1) for intertidal macrophytes. Porphyra conchocelis had lower respiration rates at 7°C than at 11°C or 15°C. All three species exhibited minimal respiration rates at salinities between 25 and 35 psu.     

Diurnal and seasonal changes in the intensity of photosynthesis in stems of lilac (Syringa vulgaris L.)

It has been demonstrated that during the whole year the stems are photosyntheticaly active and capable of assimilating atmospheric CO₂. The intensity of photosynthesis varies. During the vegetation period the registered net photosynthesis lasted up to 13 hours per day, and in the leafless period for 2–3 hours a day. Photosynthesis was registered also at temperatures below zero (−3 °C) as a reduced CO₂ evolution in light in comparison with darkness. The maximal net photosynthesis values during the vegetation period amounted to 6 up 8 μmol (CO₂)·m⁻²·s⁻¹, and in the leafless period 0.5 – 1 μmol (CO₂)·m⁻²·s⁻¹, and they were close to being up to twice as big as the values obtained of darkness respiration. An increase of the photosynthetic activity of stems preceded the spring development of the leaves.     

COMPARATIVE PHOTOSYNTHESIS OF TWO SPECIES OF INTERTIDAL EPIPHYTIC MACROALGAE ON MANGROVE ROOTS DURING SUBMERSION AND EMERSION

Photosynthesis and dark respiration rates were measured in water and in air, and the capacity to recover photosynthetic activity from emersion stress was examined for two species of intertidal, epiphytic macroalgae—Bostrychia calliptera (Montagne) Montagne and Caloglossa leprieurii (Montagne) J. Agardh—collected on prop roots of the red mangrove Rhizophora mangle L. in Buenaventura Bay, Pacific coast of Colombia. In both species, net photosynthetic rates were significantly higher under submersed conditions. Maximum photosynthetic rates (P_max) in water and in air were highest in B. calliptera, 126 ± 4 versus 52 ± 9 μmol O₂·mg chl a⁻¹·h⁻¹, respectively. In C. leprieurii, P_max of submerged plants in water and in air were 98 ± 9 versus 30 ± 11 μmol O₂·mg chla⁻¹·h⁻¹. The photoinhibition model of Platt et al. (1980) was used to fit the experimental data in both water and air for both species. Photoinhibition occurred at irradiance as low as 200 μmol·m⁻²·s⁻¹. The photosynthesis–light response curves demonstrated an adaptation to shaded habitats for both species, as light compensation points in water and air for both species were below 17 ± 5 μmol·m⁻²·s⁻¹. The rate of dehydration was significantly lower in thalli of B. calliptera compared to C. leprieurii. An increase of photosynthetic activity in B. calliptera was evident between 5% and 15% water loss, but rates decreased thereafter with declining water content. In C. leprieurii, desiccation negatively influenced photosynthetic rates that significantly decreased linearly with declining water content. In B. calliptera, net photosynthesis reached zero only at a water content between 29% and 35%, whereas in C. leprieurii no net photosynthesis occurred in plants containing less than about 50% of their relative water content. Resubmerged plants ofB. calliptera exhibited 100% photosynthetic recovery after 45 min, whereas C. leprieurii recovered 100% at about 120 min. On the basis of the comparison of rates of light-saturated net photosynthesis for B. calliptera in air versus in water, aerial photosynthetic activity ranged from 35% to 42% of that in water, whereas the emersed photosynthetic capacity of C. leprieurii ranged from 24% to 29% of that in water. Using tidal predictions and the emersed photosynthetic rates, a carbon balance model was constructed for both species over a single daylight period. The calculations indicated that emersed photosynthesis increased average daily carbon production of B. calliptera by 17% and C. leprieuri by 12%. The physiological responses to desiccation stress and the photosynthetic recovery capacities between species correlated with, and may determine, their vertical distribution in the mangrove habitats of Buenaventura Bay.     

Light respiration by subtropical seaweeds

Here, we report the first‐ever measurements of light CO₂ respiration rate (CRR) by seaweeds. We measured the influence of temperature (15–25°C) and light (irradiance from 60 to 670 μmol · m^?2 · s^?1) on the light CCR of two subtropical seaweed species, and measured the CRR of seven different seaweed species under the same light (150 μmol · m^?2 · s^?1) and temperature (25°C). There was little effect of irradiance on light CRR, but there was an effect of temperature. Across the seven species light CRR was similar to OCR (oxygen consumption rate in the dark), with the exception of a single species. The outlier species was a coralline alga, and the higher light CRR was probably driven by calcification. CRR could be estimated from OCR, as well as carbon photosynthetic rates from oxygen photosynthetic rates, which suggests that previous studies have probably provided good estimations of gross photosynthesis for seaweeds.     

Effects of temperature,salinity and body size on routine metabolism of coastal largemouth bass Micropterus salmoides

Routine metabolism (i.e. standard metabolism plus a low level of activity) of coastal largemouth bass Micropterus salmoides from Mobile‐Tensaw Delta, AL, U.S.A. was examined as a function of temperature (15, 20, 25 and 30° C), salinity (0, 4, 8 and 12) and body mass (range 24–886 g) using flow‐through respirometry. Functionally, a cubic relationship best described the effect of salinity on respiration; the magnitude of these effects increased with temperature and body mass. The best model predicted that specific respiration (mg O₂ g^?1 h^?1) at temperatures >20° C was lowest at salinities of 0·0 and 9·7, and elevated at 3·2 and 12·0; salinity had little to no effect at temperatures ≤20° C. Respiration increased exponentially with temperature, but when compared with previously published respiration rates for M. salmoides from northern latitudes, predicted respiration was higher at cool temperatures and lower at high temperatures. The reduced energetic cost near the isosmotic level (i.e. c. 9) may be an adaptive mechanism to tolerate periods of moderate salinity levels and may help explain why M. salmoides do not flee an area in response to increased salinity. Further, these results suggest that salinity has high energetic costs for coastal populations of M. salmoides and may contribute to the observed slow growth and small maximum size within coastal systems relative to inland freshwater populations.     

Inhibition of photosynthesis by chilling in the light

The photosynthetic activity of leaf slices from Spinacia oleracea L., Cucumis sativus L. and Nerium oleander L. was measured in 25° C immediately after preincubation for 2.5 h at various photon flux densities (PFD) with chilling at 4°C, or at a moderate (450 μmol m⁻² s⁻¹) PFD with various temperatures below 25°C. Inhibition of photosynthesis was evident in C. sativus and 45°C-grown N. oleander after preincubation at 4°C at all PFD. The inhibition was most severe at fluxes in excess of the moderate PFD under which the plants were grown. Photosynthesis in S. oleracea and 20°C-grown N. oleander was not inhibited at 4°C unless the PFD was in excess of this moderate PFD. The inhibition of photosynthesis was initiated in C. sativus below 13°C, and in 45°C-grown N. oleander below 8°C. A phase transition in the polar lipids from the thylakoids of these plants was detected at about the same temperatures. For S. oleracea and 20°C-grown N. oleander preincubated under the same conditions, there was no inhibition of photosynthesis and no phase transition above 0°C. These results show that some component of photosynthesis was disrupted in the light at temperatures below that of the phase transition in the thylakoid polar lipids.     

Characterization of Brackish Coastal Waters of Different Trophic Levels by Means of Phytoplankton Biomass and Primary Production

Investigations on phytoplankton have been carried out in Baltic coastal waters, which are widely separated from the sea. Corresponding to their distance to the sea they differ in their trophic level. Annual phytoplankton production and a mean biovolume of 100-200 g C · m⁻² and 2-10 mm⁻³ · 1⁻¹ respectively were found for the mesotrophic level, of 200-400 g C · m⁻² and 10-20 mm³ · 1⁻¹ for the eutrophic level, and of 400-600 g C · m⁻² and over 20 mm³ · 1⁻¹ for the polytrophic level. In the course of nearly two decades of investigation a slight increase of phytoplankton biovolume, but no increase of primary production was recorded. Some changes in species composition are to be recognized in Greifswalder Bodden, if old literature is compared with recent data. In the Darss-Zingst boddens a shift from Cyanobacteria dominance towards Chlorophyceae dominance has appeared for at least 5 years. This was on account of the disappearance of Gomphosphaeria pusilla, which is thought to be an indicator species of the mesotrophic level.     

Modulation of photosynthesis and respiration in guard and mesophyll cell protoplasts by oxygen concentration

Stomatal movement is an energetic oxygen-requiring process. In the present study, the effect of oxygen concentration on mitochondrial respiratory activity and red-light-dependent photosynthetic oxygen evolution by Vicia faba and Brassica napus guard cell protoplasts was examined. Comparative measurements were made with mesophyll cell protoplasts isolated from the same species. At air saturated levels of dissolved oxygen in the protoplast suspension media, respiration rates by mesophyll protoplasts ranged from 6 to 10μmoles O₂ mg^?1 chl h^?1, while guard cell protoplasts respired at rates of 200–300 μmoles O₂ mg chl^?1 h^?1, depending on the species. Lowering the oxygen concentration below 50–60 mmol m^?3 resulted in a decrease in guard cell respiration rates, while rates by mesophyll cell protoplasts were reduced only at much lower concentrations of dissolved oxygen. Rates of photosynthesis in mesophyll cell protoplasts isolated from both species showed only a minor reduction in activity at low oxygen concentrations. In contrast, photosynthesis by guard cell protoplasts isolated from V. faba and B. napus decreased concomitantly with respiration. Oligomycin, an inhibitor of oxidative phos-phorylation, reduced photosynthesis in mesophyll cell protoplasts by 27–46% and in guard cell protoplasts by 51–58%. The reduction in both guard cell photosynthesis and respiration following exposure to low oxygen concentrations suggest close metabolic coupling between the two activities, possibly mediated by the availability of substrate for respiration associated with photosynthetic electron transport activity and subsequent export of redox equivalents.     

Strong seasonal patterns of DOC release by a temperate seaweed community: Implications for the coastal ocean carbon cycle

Release of dissolved organic carbon (DOC) by seaweed underpins the microbial food web and is crucial for the coastal ocean carbon cycle. However, we know relatively little of seasonal DOC release patterns in temperate regions of the southern hemisphere. Strong seasonal changes in inorganic nitrogen availability, irradiance, and temperature regulate the growth of seaweeds on temperate reefs and influence DOC release. We seasonally surveyed and sampled seaweed at Coal Point, Tasmania, over 1 year. Dominant species with or without carbon dioxide (CO₂) concentrating mechanisms (CCMs) were collected for laboratory experiments to determine seasonal rates of DOC release. During spring and summer, substantial DOC release (10.06–33.54 μmol C · g DW⁻¹ · h⁻¹) was observed for all species, between 3 and 27 times greater than during autumn and winter. Our results suggest that inorganic carbon (C_i) uptake strategy does not regulate DOC release. Seasonal patterns of DOC release were likely a result of photosynthetic overflow during periods of high gross photosynthesis indicated by variations in tissue C:N ratios. For each season, we calculated a reef-scale net DOC release for seaweed at Coal Point of 7.84–12.9 g C · m⁻² · d⁻¹ in spring and summer, which was ~16 times greater than in autumn and winter (0.2–1.0 g C · m⁻² · d⁻¹). Phyllospora comosa, which dominated the biomass, contributed the most DOC to the coastal ocean, up to ~14 times more than Ecklonia radiata and the understory assemblage combined. Reef-scale DOC release was driven by seasonal changes in seaweed physiology rather than seaweed biomass.