Effects of temperature and irradiance on photosynthesis and growth of a green-tide-forming species (<Emphasis Type="Italic">Ulva linza</Emphasis>) in the Yellow Sea

Samples of the massive drifting green alga, Ulva linza, were collected from the coastal waters of the Yellow Sea, southwest of Korea, in early July 2009, and cultured under laboratory conditions. The effects of various temperature (10–30°C) and irradiance levels (0–1,000 μmol photons m⁻² s⁻¹) on photosynthesis, growth, and tissue nutrient content of U. linza were investigated in laboratory for both individuals of the late-stage vegetation (LSV) and the early-stage vegetation (ESV). After 1 h acclimation to various irradiance and temperature conditions, maximum gross photosynthetic rate of ESV was significantly higher than those of LSV. In the long-term (7-d) acclimation experiments to various irradiance and temperature levels, gross photosynthetic rates of ESV individuals were also significantly higher than those of LSV individuals. High photosynthetic rate of ESV individuals induced increase in mass of about 60% over the growth saturation irradiance (136 μmol photons m⁻² s⁻¹) and about 20% under low temperature conditions (10–15°C) during 7-d. The gross photosynthesis of LSV individuals was low when examined under temperature and irradiance conditions that were optimum for ESV growth. Consequently, free-floating U. linza exhibits cellular senescence beginning in early July in the Yellow Sea, and green tides formed by this species cannot be maintained beyond this time in the open sea. However, we expect that U. linza can proliferate quickly after settlement on new coastal habitats of the Yellow Sea because of the high tissue nitrogen utilization for photosynthesis in ESV, which is formed by germination of reproductive cells.     

Photosynthetic response and recovery of Antarctic marine benthic microalgae exposed to elevated irradiances and temperatures

Exposure to high temperatures affects the photosynthetic processes in marine benthic microalgae by limiting the transport of electrons, thus reducing the ability of the cell to use light. This causes damage to the Photosystem II (PSII) and may lead to photoinhibition. However, the PSII of benthic microalgal communities from Brown Bay, eastern Antarctica, were relatively unaffected by significant changes in temperature. Benthic microalgae exposed to temperatures up to 8°C and an irradiance of 450 μmol photons m⁻² s⁻¹ did not experience any photosynthetic damage or irreversible photoinhibition. The effective quantum yield (∆F/F _m′) at 8°C (0.433 ± 0.042) was higher by comparison to cell incubated at −0.1°C (0.373 ± 0.015) with similar irradiances. Temperatures down to −5°C at a similar irradiance showed a decrease in photosynthesis with decreasing temperature, but no severe photoinhibition as the cells were able to dissipate excess energy via non-photochemical quenching and recover from damage. These responses are consistent with those recorded in past studies on Antarctic benthic microalgae and suggest that short-term temperature change (from −5 to 8°C) will not do irreversible damage to the PSII and will not affect the photosynthesis of the benthic microalgae.     

Temperature and irradiance impacts on the growth,pigmentation and photosystem II quantum yields of <Emphasis Type="Italic">Haematococcus pluvialis</Emphasis> (Chlorophyceae)

The microalga Haematococcus pluvialis Flotow has been the subject of a number of studies concerned with maximizing astaxanthin production for use in animal feeds and for human consumption. Several of these studies have specifically attempted to ascertain the optimal temperature and irradiance combination for growth of H. pluvialis, but there has been a great deal of disagreement between laboratories. “Ideal” levels of temperature and irradiance have been reported to range from 14 to 28°C and 30 to 200 μmol photons m⁻² s⁻¹. The objective of the present study was to simultaneously explore temperature and irradiance effects for a single strain of H. pluvialis (UTEX 2505) across an experimental region that encompassed the reported “optimal” combinations of these factors for multiple strains. To this end, a two-dimensional experimental design based on response surface methodology (RSM) was created. Maximum growth rates for UTEX 2505 were achieved at 27°C and 260 μmol photons m⁻² s⁻¹, while maximum quantum yield for stable charge separation at PSII (F_v/F_m) was achieved at 27°C and 80 μmol photons m⁻² s⁻¹. Maximum pigment concentrations correlated closely with maximum F_v/F_m. Numeric optimization of growth rate and F_v/F_m produced an optimal combination of 27°C and 250 μmol photons m⁻² s⁻¹. Polynomial models of the various response surfaces were validated with multiple points and were found to be very useful for predicting several H. pluvialis UTEX 2505 responses across the entire two-dimensional experimental design space.     

Effects of light and temperature on the attachment and development of <Emphasis Type="BoldItalic">Gloiopeltis tenax</Emphasis> and <Emphasis Type="BoldItalic">Gloiopeltis furcata</Emphasis> tetraspores

Two 60-day experiments were conducted to study the influence of photon flux density (PFD) and temperature on the attachment and development of Gloiopeltis tenax and Gloiopeltis furcata tetraspores. In the first experiment, tetraspores of the two Gloiopeltis species were incubated at five temperature ranges (8°C, 12°C, 16°C, 20°C, 24°C) under a constant PFD of 80 μmol photons m⁻² s⁻¹ with a photoperiod of 12:12. In a second experiment, tetraspores were incubated under five PFD gradients (30, 55, 80, 105, 130 μmol photons m⁻² s⁻¹) at a constant temperature of 16°C with a photoperiod of 12:12. Maximum density of attached tetraspores was observed at 16°C for both species. Maximum per cent of spore germinating into disc was recorded at 12–16°C for G. tenax and 8–12°C for G. furcata. Maximum per cent of discs producing erect axes for G. tenax and G. furcata were recorded at 24°C and 20°C, respectively. Light had no significant effect on tetraspore attachment and developing into disc, but it affected the growth, sprouting and survival of its discs. Under 30–55 μmol photons m⁻² s⁻¹, the discs of the two species of Gloiopeltis did not form thallus until the end of the experiment. Optimum PFD range for G. tenax discs was 80–105 μmol photons m⁻² s⁻¹, whilst it was 80–130 μmol photons m⁻² s⁻¹ for G. furcata. Results presented in this study are expected to assist the progress of artificial seeding of Gloiopeltis.     

Effects of temperature on photosynthesis of two morphologically contrasting plant species along an altitudinal gradient in the tropical high Andes

The effects of temperature on photosynthesis of a rosette plant growing at ground level, Acaena cylindrostachya R. et P., and an herb that grows 20–50 cm above ground level, Senecio formosus H.B.K., were studied along an altitudinal gradient in the Venezuelan Andes. These species were chosen in order to determine – in the field and in the laboratory – how differences in leaf temperature, determined by plant form and microenvironmental conditions, affect their photosynthetic capacity. CO₂ assimilation rates (A) for both species decreased with increasing altitude. For Acaena leaves at 2900 m, A reached maximum values above 9 μmol m⁻² s⁻¹, nearly twice as high as maximum A found at 3550 m (5.2) or at 4200 m (3.9). For Senecio leaves, maximum rates of CO₂ uptake were 7.5, 5.8 and 3.6 μmol m⁻² s⁻¹ for plants at 2900, 3550 and 4200 m, respectively. Net photosynthesis-leaf temperature relations showed differences in optimum temperature for photosynthesis (A _o.t.) for both species along the altitudinal gradient. Acaena showed similar A _o.t. for the two lower altitudes, with 19.1°C at 2900 m and 19.6°C at 3550 m, while it increased to 21.7°C at 4200 m. Maximum A for this species at each altitude was similar, between 5.5 and 6.0 μmol m⁻² s⁻¹. For the taller Senecio, A _o.t. was more closely related to air temperatures and decreased from 21.7°C at 2900 m, to 19.7°C at 3550 m and 15.5°C at 4200 m. In this species, maximum A was lower with increasing altitude (from 6.0 at 2900 m to 3.5 μmol m⁻² s⁻¹ at 4200 m). High temperature compensation points for Acaena were similar at the three altitudes, c. 35°C, but varied in Senecio from 37°C at 2900 m, to 39°C at 3550 m and 28°C at 4200 m. Our results show how photosynthetic characteristics change along the altitudinal gradient for two morphologically contrasting species influenced by soil or air temperatures. Received: 5 July 1997 / Accepted: 25 October 1997     

Deschampsia antarctica Desv. primary photochemistry performs differently in plants grown in the field and laboratory

Primary photochemistry of photosystem II (F _v/F _m) of the Antarctic hair grass Deschampsia antarctica growing in the field (Robert Island, Maritime Antarctic) and in the laboratory was studied. Laboratory plants were grown at a photosynthetic photon flux density (PPFD) of 180 μmol m⁻² s⁻¹ and an optimal temperature (13 ± 1.5°C) for net photosynthesis. Subsequently, two groups of plants were exposed to low temperature (4 ± 1.5°C day/night) under two levels of PPFD (180 and 800 μmol m⁻² s⁻¹) and a control group was kept at 13 ± 1.5°C and PPFD of 800 μmol m⁻² s⁻¹. Chlorophyll fluorescence was measured during several days in field plants and weekly in the laboratory plants. Statistically significant differences were found in F _v/F _m (=0.75–0.83), F ₀ and F _m values of field plants over the measurement period between days with contrasting irradiances and temperature levels, suggesting that plants in the field show high photosynthetic efficiency. Laboratory plants under controlled conditions and exposed to low temperature under two light conditions showed significantly lower F _v/F _m and F _m. Moreover, they presented significantly less chlorophyll and carotenoid content than field plants. The differences in the performance of the photosynthetic apparatus between field- and laboratory-grown plants indicate that measurements performed in ex situ plants should be interpreted with caution.     

Photosynthetic responses of apricot (<Emphasis Type="Italic">Prunus armeniaca</Emphasis> L.) to photosynthetic photon flux density,leaf temperature,and CO<Subscript>2</Subscript> concentration

Two cultivars (Katy and Erhuacao) of apricot (Prunus armeniaca L.) were evaluated under open-field and solar-heated greenhouse conditions in northwest China, to determine the effect of photosynthetic photon flux density (PPFD), leaf temperature, and CO₂ concentration on the net photosynthetic rate (P _N). In greenhouse, Katy registered 28.3 μmol m⁻² s⁻¹ for compensation irradiance and 823 μmol m⁻² s⁻¹ for saturation irradiance, which were 73 and 117 % of those required by Erhuacao, respectively. The optimum temperatures for cvs. Katy and Erhuacao were 25 and 35 °C in open-field and 22 and 30 °C in greenhouse, respectively. At optimal temperatures, P _N of the field-grown Katy was 16.5 μmol m⁻² s⁻¹, 21 % less than for a greenhouse-grown apricot. Both cultivars responded positively to CO₂ concentrations below the CO₂ saturation concentration, whereas Katy exhibited greater P _N (18 %) and higher carboxylation efficiency (91 %) than Erhuacao at optimal CO₂ concentration. Both cultivars exhibited greater photosynthesis in solar-heated greenhouses than in open-field, but Katy performed better than Erhuacao under greenhouse conditions.     

Photosynthetic and respiratory responses of Gracilaria vermiculophylla (Ohmi) Papenfuss collected from Kumamoto, Shizuoka and Iwate, Japan

The photosynthetic and respiratory responses to irradiance, salinity and temperature of the red alga, Gracilaria vermiculophylla, collected from Kumamoto, Shizuoka and Iwate in Japan were studied using an electronic Dissolved Oxygen sensor. The parameters derived from the photosynthesis versus irradiance relationship indicated the potential to acclimate to broad irradiance variations in all of the populations of G. vermiculophylla collected from these three sites. In addition, the light-saturated photosynthesis rate (P _max) and the dark respiration rate of all populations increased with increasing temperature up to 20–30°C, while the P _max decreased at 35°C. All populations also showed a broad variation of photosynthetic responses to salinity changes in the range from 10 to 30 psu. On the other hand, the population from Iwate showed high photosynthetic efficiency, especially in the temperature range of 5–10°C, and showed low values of saturation irradiance compared to the populations from Shizuoka and Kumamoto. These results suggest that there is greater potential to acclimate to low irradiance and low temperature in the population from Iwate compared to those from the Shizuoka and Kumamoto populations. However, the P _max of the populations from Iwate and Shizuoka was reached at 20°C and 25°C, respectively, while the Kumamoto population reached P _max at 30°C. This implies that the latter population has greater potential to tolerate higher temperatures than the former. Such characteristics in photosynthesis and respiration of G. vermiculophylla collected from the three locations probably indicate an acclimation to prevailing environmental conditions in their respective habitats.     

Growing season temperatures limit growth of loblolly pine (Pinus taeda L.) seedlings across a wide geographic transect

We grew potted loblolly pine (Pinus taeda L.) seedlings from a single provenance under well watered and fertilized conditions at four locations along a 610 km north–south transect that spanned most of the species range to examine how differences in the above-ground environment would affect growth rate, biomass partitioning and gas exchange characteristics. Across the transect there was an 8.7°C difference in average growing season temperature, and temperature proved to be the key environmental factor controlling growth rate. Biomass growth was strongly correlated with differences in mean growing season temperature (R ² = 0.97) and temperature sum (R ² = 0.92), but not with differences in mean daily photosynthetic photon flux density or mean daily vapor pressure deficit. Biomass partitioning between root and shoot was unchanged across sites. There was substantial thermal acclimation of leaf respiration, but not photosynthesis. In mid-summer, leaf respiration rates measured at 25°C ranged from 0.2 μmol m⁻² s⁻¹ in seedlings from the warmest location to 1.1 μmol m⁻² s⁻¹ in seedlings from the coolest site. The greatest biomass growth occurred near the middle of the range, indicating that temperatures were sub- and supra-optimal at the northern and southern ends on the range, respectively. However, in the middle of the range, there was an 18% decrease in biomass increment between two sites, corresponding to 1.4°C increase in mean growing season temperature. This suggests that thermal acclimation was insufficient to compensate for this relatively small increase in temperature.     

Seasonal photosynthetic performance of the endemic antarctic red algaPalmaria decipiens (Reinsch) Ricker

 A male gametophyte of the endemic Antarctic red macroalga Palmaria decipiens (Reinsch) Ricker was cultivated under fluctuating daylengths, simulating the seasonal changes at the site of collection (King George Island, Antarctica). The plant was maintained at 0±1°C, an irradiance of 25 μmol m^-2 s^-1 and under growth-saturating nutrient conditions. Samples were taken at intervals of 3–6 weeks to measure growth, photosynthesis, dark respiration and pigment content. The growth optimum in spring coincided with a higher photosynthetic activity. Whereas dark respiration was constantly low over the year, there was a rapid increase in maximum photosynthetic rate (P_max) in conditions corresponding to September and October. This was correlated with a change in the initial slope (α) of the photosynthesis versus irradiance (P vs I) curve. Higher activity in photosynthesis mainly resulted from higher Chl a and phycobilin concentrations during Antarctic spring, an indication of an increase in absorption cross-section areas of photosynthetic reaction centres. These changes in physiology are discussed in relation to the seasonal growth “strategy” of the species, which is controlled by seasonal variation in daylength. Received: 27 February 1995/Accepted 3 October 1995     

Leaf photosynthesis, plant growth and nitrogen allocation in rice under different irradiances

The photosynthetic rates and various components of photosynthesis including ribulose-1,5-bisphosphate carboxylase (Rubisco; EC 4.1.1.39), chlorophyll (Chl), cytochrome (Cyt) f, and coupling factor 1 (CF₁) contents, and sucrose-phosphate synthase (SPS; EC 2.4.1.14) activity were examined in young, fully expanded leaves of rice (Oryza sativa L.) grown hydroponically under two irradiances, namely, 1000 and 350 μmol quanta · m⁻² · s⁻¹, at three N concentrations. The light-saturated rate of photosynthesis measured at 1800 μmol · m⁻² · s⁻¹ was almost the same for a given leaf N content irrespective of growth irradiance. Similarly, Rubisco content and SPS activity were not different for the same leaf N content between irradiance treatments. In contrast, Chl content was significantly greater in the plants grown at 350 μmol · m⁻² · s⁻¹, whereas Cyt f and CF₁ contents tended to be slightly smaller. However, these changes were not substantial, as shown by the fact that the light-limited rate of photosynthesis measured at 350 μmol · m⁻² · s⁻¹ was the same or only a little higher in the plants grown at 350 μmol · m⁻² · s⁻¹ and that CO₂-saturated photosynthesis did not differ between irradiance treatments. These results indicate that growth-irradiance-dependent changes in N partitioning in a leaf were far from optimal with respect to N-use efficiency of photosynthesis. In spite of the difference in growth irradiance, the relative growth rate of the whole plant did not differ between the treatments because there was an increase in the leaf area ratio in the low-irradiance-grown plants. This increase was associated with the preferential N-investment in leaf blades and the extremely low accumulation of starch and sucrose in leaf blades and sheaths, allowing a more efficient use of the fixed carbon. Thus, morphogenic responses at the whole-plant level may be more important for plants as an adaptation strategy to light environments than a response of N partitioning at the level of a single leaf. Received: 23 February 1997 / Accepted: 8 May 1997     

Physiological differences in the growth of <Emphasis Type="Italic">Sargassum horneri</Emphasis> between the germling and adult stages

The effects of temperature, irradiance, and daylength on Sargassum horneri growth were examined at the germling and adult stages to discern their physiological differences. Temperature–irradiance (10, 15, 20, 25, 30°C × 20, 40, 80 μmol photons m⁻²s⁻¹) and daylength (8, 12, 16, 24 h) experiments were carried out. The germlings and blades of S. horneri grew over a wide range of temperatures (10–25°C), irradiances (20–80 μmol photons m⁻²s⁻¹), and daylengths (8–24 h). At the optimal growth conditions, the relative growth rates (RGR) of the germlings were 21% day⁻¹ (25°C, 20 μmol photons m⁻²s⁻¹) and 13% day⁻¹ (8 h daylength). In contrast, the RGRs of the blade weights were 4% day⁻¹ (15°C, 20 μmol photons m⁻²s⁻¹) and 5% day⁻¹ (12 h daylength). Negative growth rates were found at 20 μmol photons m⁻²s⁻¹ of 20°C and 25°C treatments after 12 days. This phenomenon coincides with the necrosis of S. horneri blades in field populations. In conclusion, we found physiological differences between S. horneri germlings and adults with respect to daylength and temperature optima. The growth of S. horneri germlings could be enhanced at 25°C, 20 μmol photons m⁻²s⁻¹, and 8 h daylength for construction of Sargassum beds and restoration of barren areas.     

Protein,fatty acid,and pigment content of <Emphasis Type="Italic">Chlorella vulgaris</Emphasis> under different light regimes

The effects of irradiance and photoperiod on growth rates, chlorophyll a, β-carotene, total protein, and fatty acid content of Chlorella vulgaris were determined. The maximum growth rate (1.13 day⁻¹) was at 100 μmol photons m⁻² s⁻¹ and 16:8-h light/dark photoperiod. Chlorophyll a and β-carotene contents significantly differed under different light regimes with chlorophyll a content lower at high irradiance and longer light duration, while β-carotene showed the inverse trend. The total protein and fatty acid content also significantly differed in different light regimes; the maximum percentage of protein (46%) was at 100 μmol photons m⁻² s⁻¹ and 16:8 h photoperiod, and minimum (33%) was at 37.5 μmol photons m⁻² s⁻¹ and 8:16 h photoperiod; the total saturated fatty acids increased, while monounsaturated and polyunsaturated fatty acids decreased with increasing irradiance and light duration.     

Microphytobenthos of Arctic Kongsfjorden (Svalbard, Norway): biomass and potential primary production along the shore line

During summer 2007, Arctic microphytobenthic potential primary production was measured at several stations around the coastline of Kongsfjorden (Svalbard, Norway) at ≤5 m water depth and at two stations at five different water depths (5, 10, 15, 20, 30 m). Oxygen planar optode sensor spots were used ex situ to determine oxygen exchange in the overlying water of intact sediment cores under controlled light (ca. 100 μmol photons m⁻² s⁻¹) and temperature (2–4°C) conditions. Patches of microalgae (mainly diatoms) covering sandy sediments at water depths down to 30 m showed high biomass of up to 317 mg chl a m⁻². In spite of increasing water depth, no significant trend in “photoautotrophic active biomass” (chl a, ratio living/dead cells, cell sizes) and, thus, in primary production was measured at both stations. All sites from ≤5 to 30 m water depth exhibited variable rates of net production from −19 to +40 mg O₂ m⁻² h⁻¹ (−168 to +360 mg C m⁻² day⁻¹) and gross production of about 2–62 mg O₂ m⁻² h⁻¹ (17–554 mg C m⁻² day⁻¹), which is comparable to other polar as well as temperate regions. No relation between photoautotrophic biomass and gross/net production values was found. Microphytobenthos demonstrated significant rates of primary production that is comparable to pelagic production of Kongsfjorden and, hence, emphasised the importance as C source for the zoobenthos.     

Characterization of hyperthermostable α-amylase from Geobacillus sp. IIPTN

A newly isolated Geobacillus sp. IIPTN (MTCC 5319) from the hot spring of Uttarakhand's Himalayan region produced a hyperthermostable α-amylase. The microorganism was characterized by biochemical tests and 16S rRNA gene sequencing. The optimal temperature and pH were 60°C and 6.5, respectively, for growth and enzyme production. Although it was able to grow in temperature ranges from 50 to 80°C and pH 5.5–8.5. Maximum enzyme production was in exponential phase with activity 135 U ml⁻¹ at 60°C. Assayed with cassava as substrate, the enzyme displayed optimal activity 192 U ml⁻¹ at pH 5.0 and 80°C. The enzyme was purified to homogeneity with purification fold 82 and specific activity 1,200 U mg⁻¹ protein. The molecular mass of the purified enzyme was 97 KDa. The values of K _m and V _max were 36 mg ml⁻¹ and 222 μmol mg⁻¹ protein min⁻¹, respectively. The amylase was stable over a broad range of temperature from 40°C to 120°C and pH ranges from 5 to 10. The enzyme was stimulated with Mn²⁺, whereas it was inhibited by Hg²⁺, Cu²⁺, Zn²⁺, Mg²⁺, and EDTA, suggesting that it is a metalloenzyme. Besides hyperthermostability, the novelty of this enzyme is resistance against protease.     

Energy Budget for the Cultured,Zooxanthellate Octocoral <Emphasis Type="Italic">Sinularia flexibilis</Emphasis>

The zooxanthellate octocoral Sinularia flexibilis is a producer of potential pharmaceutically important metabolites such as antimicrobial and cytotoxic substances. Controlled rearing of the coral, as an alternative for commercial exploitation of these compounds, requires the study of species-specific growth requirements. In this study, phototrophic vs. heterotrophic daily energy demands of S. flexibilis was investigated through light and Artemia feeding trials in the laboratory. Rate of photosynthetic oxygen by zooxanthellae in light (≈200 μmol quanta m⁻² s⁻¹) was measured for the coral colonies with and without feeding on Artemia nauplii. Respiratory oxygen was measured in the dark, again with and without Artemia nauplii. Photosynthesis–irradiance curve at light intensities of 0, 50, 100, 200, and 400 μmol quanta m⁻² s⁻¹ showed an increase in photosynthetic oxygen production up to a light intensity between 100 and 200 μmol quanta m⁻² s⁻¹. The photosynthesis to respiration ratio (P/R > 1) confirmed phototrophy of S. flexibilis. Both fed and non-fed colonies in the light showed high carbon contribution by zooxanthellae to animal (host) respiration values of 111–127%. Carbon energy equivalents allocated to the coral growth averaged 6–12% of total photosynthesis energy (mg C g ⁻ 1 buoyant weight day ⁻ 1) and about 0.02% of the total daily radiant energy. “Light utilization efficiency (ε)” estimated an average ε value of 75% 12 h ⁻ 1 for coral practical energetics. This study shows that besides a fundamental role of phototrophy vs. heterotrophy in daily energy budget of S. flexibilis, an efficient fraction of irradiance is converted to useable energy.     

Light acclimatisation of Elodea nuttallii grown under ambient DIC conditions

Light acclimatisation capabilities of Elodea nuttallii at nearly ambient DIC conditions were investigated by determining growth characteristics, main photosynthetic parameters and pigmentation of plants incubated at 5 different irradiances (10–146 μmol photons m⁻² s⁻¹). Positive net growth was observed under all light treatments tested. Maximum ratio root versus shoot (r:s) of 1.86 was achieved at medium irradiances (72–94 μmol photons m⁻² s⁻¹), whereas at low (10 μmol photons m⁻² s⁻¹) and high irradiances (146 μmol photons m⁻² s⁻¹) r:s was significantly lower (0.39 and 1.05, respectively). With respect to main photosynthetic parameters, an increase of light compensation points (E _c), attended by decreasing ratios of light saturation points of photosynthesis (E _k)/irradiance were observed. E _c values were comparable to other low-light adapted macrophytes, which indicate that E. nuttallii can be regarded as a low-light adapted plant, under photorespiratory conditions. This was also confirmed by maximum E _k values of just 73 μmol photons m⁻² s⁻¹. Further support was achieved from pigmentation and non-photochemical quenching (NPQ) data, both indicating rather limited acclimatisation ability at light treatments above 90 μmol photons m⁻² s⁻¹. These results are discussed with respect to the competitive abilities of E. nuttallii under nearly ambient (photorespiratory) DIC conditions, especially in dense stands and turbid phytoplankton-dominated waters.     

Synergistic effect of high-light and low temperature on cell growth of the Δ12 fatty acid desaturase mutant in Synechococcus sp. PCC 7002

The effect of polyunsaturated fatty acids on photosynthesis and the growth of the marine cyanobacterium Synechococcus sp. PCC 7002 was examined using wild-type and Δ12 fatty acid desaturase mutant strains. Under a light intensity of 250 μmol m⁻² s⁻¹, wild-type cells could grow exponentially in a temperature range of 20–38 °C, but growth was non-exponential below 20 °C and ceased at 12 °C. The Δ12 desaturase mutant cells lacking polyunsaturated fatty acids had the same growth rate as wild-type cells in a temperature range of 25–38 °C but grew slowly at 22 °C, and no cell growth took place below 18 °C. Under a very high-light intensity of 2.5 mmol m⁻² s⁻¹, wild-type cells could grow exponentially in a temperature range of 30–38 °C, although the high-light grown cells became chlorotic because of nitrogen limitation. The temperature sensitive phenotype in the Δ12 desaturase mutant was enhanced in cells grown under high-light illumination; the mutant cells could grow at 38 °C, but were killed at 30 °C. The decrease of oxygen evolution and nitrate consumption by whole cells as a function of temperature was similar in both wild type and the Δ12 desaturase mutant. No differences were observed in either light-induced damage of oxygen evolution or recovery from this damage. No inactivation of oxygen evolution took place at 22 °C under the normal light intensity of 250 μmol m⁻² s⁻¹. These results suggest that growth of the Δ12 desaturase mutant at low temperature is not directly limited by the inactivation of photosynthesis, and raise new questions about the functions of polyunsaturated membrane lipids on low temperature acclimation in cyanobacteria. This revised version was published online in June 2006 with corrections to the Cover Date.     

Interactive Effects of CO2, Temperature,Irradiance, and Nutrient Limitation on the Growth and Physiology of the Marine Diatom Thalassiosira pseudonana (Coscinodiscophyceae)

The marine diatom Thalassiosira pseudonana was grown in continuous culture systems to study the interactive effects of temperature, irradiance, nutrient limitation, and the partial pressure of CO₂ (pCO₂) on its growth and physiological characteristics. The cells were able to grow at all combinations of low and high irradiance (50 and 300 μmol photons · m⁻² · s⁻¹, respectively, of visible light), low and high pCO₂ (400 and 1,000 μatm, respectively), nutrient limitation (nitrate-limited and nutrient-replete conditions), and temperatures of 10–32°C. Under nutrient-replete conditions, there was no adverse effect of high pCO₂ on growth rates at temperatures of 10–25°C. The response of the cells to high pCO₂ was similar at low and high irradiance. At supraoptimal temperatures of 30°C or higher, high pCO₂ depressed growth rates at both low and high irradiance. Under nitrate-limited conditions, cells were grown at 38 ± 2.4% of their nutrient-saturated rates at the same temperature, irradiance, and pCO₂. Dark respiration rates consistently removed a higher percentage of production under nitrate-limited versus nutrient-replete conditions. The percentages of production lost to dark respiration were positively correlated with temperature under nitrate-limited conditions, but there was no analogous correlation under nutrient-replete conditions. The results suggest that warmer temperatures and associated more intense thermal stratification of ocean surface waters could lower net photosynthetic rates if the stratification leads to a reduction in the relative growth rates of marine phytoplankton, and at truly supraoptimal temperatures there would likely be a synergistic interaction between the stresses from temperature and high pCO₂ (lower pH).     

Carpospore early development and callus-like tissue induction of <Emphasis Type="Italic">Chrysymenia wrightii</Emphasis> (Rhodymeniaceae,Rhodophyta) under laboratory conditions

Morphological and culture studies of germlings derived from carpospores of Chrysymenia wrightii (Harvey) Yamada were carried out under various treatments combining temperature and irradiance. Basal, main, and tip branches were applied for inducing callus-like tissue. Focus was on how carpospores develop into germlings, how callus-like tissues are induced from explants, and how temperature and irradiance affect carpospore germination and discoid crust growth. Results show that carpospore development can be divided into three stages: division stage, discoid crust stage, and erect juvenile germling stage. Discoid crusts, even more than ten, might coalesce into a big discoid crust, and then developed into germlings. Filamentous fronds, formed on the rims of discoid crusts, exhibited in self-existence or co-existence form with germlings, could form spherical tufts if cultured separately. Filamentous callus-like tissues appeared on the tip branches after 13 days. PES is suitable for filament induction and culture, and filaments have potential use in germplasm preservation and vegetative propagation. Temperature (10, 15, 20, 25°C) and irradiance (8 and 36 μmol photons m⁻² s⁻¹) significantly influenced carpospore germination rate and discoid crust diameter. Carpospores germinated normally under 36 μmol photons m⁻² s⁻¹, 15~25°C, and maximum growth of discoid crusts was at 25°C, 36 μmol photons m⁻² s⁻¹; 10°C and 8 μmol photons m⁻² s⁻¹ did not favor carpospore germination or discoid crust growth.