Trophic status of Tilitso,a high altitude Himalayan lake

The trophic status and water quality of Lake Tilitso (4920 m above sea level) in a high altitude region in central Nepal were surveyed in September, 1984. The lake is rather large with a maximum depth of 95 m and a surface area of 10.2 km². The lake water was turbid due to glacier silt and the euphotic layer was only 5 m deep. The nutrient concentration was very low with total phosphorus concentration 1–6 μg l⁻¹, and DTN concentration 0.10–0.22 mg l⁻¹. The phytoplankton biomass and chlorophyll-a concentration were also low. Primary production was estimated to be about 12 mg C m⁻² d⁻¹. The concentrations of particulate matter and most cations and bacterial number were higher in the epilimnion than in the hypolimnion. The trophic status of this lake was estimated as ultraoligotrophic.     

Environmental and nutritional factors which regulate population dynamics and toxin production in the dinoflagellate Alexandrium catenella

The effects of environmental and nutritional factors on population dynamics and toxin production were examined in Alexandrium catenella, maintained in enriched K media in laboratory cultures. Starting with a density of 50 cell ml⁻¹, the dinoflagellate population typically showed a lag phase and an exponential growth phase which lasted 14 days each, and then entered the stationary phase, with a maximal capacity of 12–18,000 cell ml⁻¹-. Population densities showed distinct diurnal patterns, with population growth beginning 2–4 hours in darkness. The optimal physical conditions for growth were pH 8.5,salinity of 30–35‰, temperature of 20–25°C, and photoperiod of 14//10D to 16L/8D. The cell cycle was determined by flow cytometry on synchronized batch cultures maintained at optimal pH, salinity, temperature and under 5 different photoperiod regimes. It was found that the G₁ phase was timed to end at approximately 3 h after onset of darkness, and the G₂/M phase had begun at 4 hours. Nutrient supply markedly affected population growth. Under optimal physical conditions, the optimal concentrations for macronutrients and micronutrients were: NH⁺⁻⁴- 0.025–0.2 mM,NO⁻³ 0.22–8.83 mM, glycerophosphate0.04–0.06 mM, silicate 0.1–0.54 mM; FeEDTA 0.07–0.11 mM;Co 0.1 μM, Cu 0.005–0.04 μM; Mn 0.22–7.2 μM;Mo 0.03–0.6 μM; Se 0.02–0.1 μM; Zn 0.04–1.6μM; thiamin 0.075–6 μM; vitamin B₁₂0.0004–0.004 μM; biotin 0.007–0.015 μM; EDTA5–40 μM. The toxin profile of A. catenella was determined by HPLC and found to include in descending order: GTX-4, GTX-3, GTX-1, B2, neosaxitoxin, saxitoxin. Toxin content per cell was highest in cell populations in the early exponential phase. The highest toxin per litre medium was recorded at 20°C at the beginning of the stationary phase,when cell density was highest and toxin/cell was still relatively high. At10°C, the cell density was low while the amount of toxin/cell was high;while at 30°C, the population at full capacity was low and the toxin/cell was also low. The population and toxin data thus provided an explanation for the peak level of PSP contamination in shellfish during the months of March–April around the eastern and southern side of Hong Kong and a minor peak extending to the western side in September–October, when the physical conditions of the seawater provided the right environment for toxin accumulation. Toxin content in the dinoflagellate reached its maximum during the S-phase of the cell cycle. Nitrogen restriction in the medium reduced population growth and toxin production, while phosphorus restriction reduced only population growth but enhanced toxin accumulation in the cells. This revised version was published online in August 2006 with corrections to the Cover Date.     

Coupled effects of irradiance and iron on the growth of a harmful algal bloom-causing microalga Scrippsiella trochoidea

Effects of irradiance and iron on the growth of a typical harmful algal blooms (HABs) causative dinoflagellate, Scrippsiella trochoidea, were investigated under various irradiances (high light: 70 μmol m^?2 s^?1 and low light: 4 μmol m^?2 s^?1) and iron concentrations (low iron: 0.063 mg L^?1, medium iron: 0.63 mg L^?1 and high iron: 6.3 mg L^?1), and evaluated by the parameters of algal cell density, specific growth rate, optical density and chlorophyll a content. The results indicated that there was significant difference in the cell density of dinoflagellate S. trochoidea between high light and low light intensity treatments across the entire experiments, 7-fold higher at high irradiance as compared with low irradiance, which was further enhanced by the iron concentration. It was found that the maximum cell density of 25 × 10⁴ cell mL^?1 occurred under the combination of high light intensity and high iron concentration, followed by 23 × 10⁴ cell mL^?1 in the combination of high light and medium iron, and 20 × 10⁴ cell mL^?1 in the combination of high light and low iron. There was no significant effect of iron concentration on the cell density under low light intensity. The cell density maintained about 3 × 10⁴ cell mL^?1 across all combinations of iron concentrations and low light in the end of experiments. Such interactive effects of light intensity and iron level dependent were also observed for the specific growth rate, OD₆₈₀ and chlorophyll a content of S. trochoidea. The maximum values of specific growth rate, OD₆₈₀ and chlorophyll a content peaked at the condition of high irradiance and high iron, which were 0.22 d^?1, 0.282 and 0.673 mg L^?1, respectively. In general, their values increased significantly with the increasing of iron concentration at high irradiance, whereas no significant difference was observed among three iron concentrations at low irradiance, all remaining approximately 0.06 d^?1, 0.03 and 0.050 mg L^?1, respectively. Those results suggest that there may be a strong interactive effect between irradiance and iron on microalgal growth and their physiological characteristics. The combination of high light and high iron concentration may accelerate algal cell growth and pigment biosynthesis, thus leading to massive occurrence of HABs.     

Coupled effects of irradiance and iron on the growth of a harmful algal bloom-causing microalga Scrippsiella trochoidea

Effects of irradiance and iron on the growth of a typical harmful algal blooms (HABs) causative dinoflagellate, Scrippsiella trochoidea, were investigated under various irradiances (high light: 70 μmol m^?2 s^?1 and low light: 4 μmol m^?2 s^?1) and iron concentrations (low iron: 0.063 mg L^?1, medium iron: 0.63 mg L^?1 and high iron: 6.3 mg L^?1), and evaluated by the parameters of algal cell density, specific growth rate, optical density and chlorophyll a content. The results indicated that there was significant difference in the cell density of dinoflagellate S. trochoidea between high light and low light intensity treatments across the entire experiments, 7-fold higher at high irradiance as compared with low irradiance, which was further enhanced by the iron concentration. It was found that the maximum cell density of 25 × 10⁴ cell mL^?1 occurred under the combination of high light intensity and high iron concentration, followed by 23 × 10⁴ cell mL^?1 in the combination of high light and medium iron, and 20 × 10⁴ cell mL^?1 in the combination of high light and low iron. There was no significant effect of iron concentration on the cell density under low light intensity. The cell density maintained about 3 × 10⁴ cell mL^?1 across all combinations of iron concentrations and low light in the end of experiments. Such interactive effects of light intensity and iron level dependent were also observed for the specific growth rate, OD₆₈₀ and chlorophyll a content of S. trochoidea. The maximum values of specific growth rate, OD₆₈₀ and chlorophyll a content peaked at the condition of high irradiance and high iron, which were 0.22 d^?1, 0.282 and 0.673 mg L^?1, respectively. In general, their values increased significantly with the increasing of iron concentration at high irradiance, whereas no significant difference was observed among three iron concentrations at low irradiance, all remaining approximately 0.06 d^?1, 0.03 and 0.050 mg L^?1, respectively. Those results suggest that there may be a strong interactive effect between irradiance and iron on microalgal growth and their physiological characteristics. The combination of high light and high iron concentration may accelerate algal cell growth and pigment biosynthesis, thus leading to massive occurrence of HABs.     

Response of Saccharomyces cerevisiae to lead ion stress

The response of Saccharomyces cerevisiae to different concentrations of Pb²⁺ was investigated. The results demonstrated that the growth of S. cerevisiae in the presence of Pb²⁺ showed a lag phase much longer than that in the absence of Pb²⁺. The inhibition was dependent upon Pb²⁺ concentrations. The Pb²⁺ at a concentration of 5 μM inhibited the microbial growth by approximately 30% with regard to control, whereas Pb²⁺ at concentration of 2 μM did not have a significant effect on the microbial growth. The existence of Pb²⁺ did not perturb cell-protein synthesis and there was a good correlation between dry cell weights and total protein content (R ² = 0.98). The RNA/DNA ratio in the microbial cells varied with Pb²⁺ concentration and there was a significant positive correlation between Pb²⁺ concentration and the RNA/DNA ratio. The microbial assimilation of ammonium ion was inhibited by the presence of Pb²⁺ in the medium; when Pb²⁺ concentration was 10 μM, the microbial ammonium assimilation was inhibited about 50%, in comparison with the control experiment.     

Cadmium and zinc uptake,growth, and primary production inCoscinodiscus granii cultures containing low levels of cells and dissolved organic carbon

Coscinodiscus granii Gough was cultivated at low cell densities in aged Atlantic sea water containing very little dissolved organic carbon; the water was enriched with low levels of nutrients but no chelators were added. Cadmium additions provided final concentrations of 0.1 to 26.5 μg Cd l⁻¹, zinc being kept constant at a level of 38 μg Zn l⁻¹. Carrier-free¹⁰⁹Cd and⁶⁵Zn were used as tracers for the two metals. Growth in terms of cell numbers and primary productivity capacity, using the¹⁴C uptake rate, was followed during the exponential growth phase for the first 5 days of the experiment and then for a further 3 days during the stationary phase. On each day, the metal contents of the cells were determined. Cadmium concentrations of 20 μg Cd l⁻¹ and more resulted in growth inhibition whereas 17.5 μg Cd l⁻¹ reduced the growth only slightly. The physiological state of the cells influenced the heavy-metal uptake per cell at sublethal Cd levels. Dead cells had a higher heavy-metal concentration than living cells. Microscopical observations revealed that cells just about to divide were less sensitive to a given toxic heavy-metal concentration than cells which had recently divided. This might have been due to different surface/volume ratios.     

Cadmium effects and accumulation in cultures ofProrocentrum micans (dinophyta)

Effects and accumulation of cadmium were studied in unialgal 10-1 batch-culture experiments with the dinoflagellateProrocentrum micans Ehrenberg. Tests were made using sterile filtered North Sea water enriched with nitrate and phosphate only in order to avoid disturbances by complex formation. Cadmium was added to the cultures in amounts of 100 to 0.13μg l⁻¹. In one series it was added at the start of the experiments and in a second one after a growth period of 1 week. Addition of only 1.2μg Cd l⁻¹ reduces multiplication rates and maximum cell densities of the algae. Not until 0.4μg Cd⁻¹ does growth correspond to that of the controls. Cadmium concentrations were measured, after filtration, in the culture medium and in the biomass by means of flameless AAS. The cadmium content in algae increased from 2.7μg g⁻¹ (dry weight) in controls to 500μg g⁻¹ (dry weight) in media containing 100μg Cd l⁻¹. Uptake occurred rapidly during the first few days of the experiments, slowed down somewhat during exponential growth stage, and increased during decay of the cultures. Cadmium content of culture media remained nearly constant (Series 1) or decreased only slowly during experimental time (Series 2). The highest concentration factor was measured in the controls. It decreased with increasing metal concentration in the medium and increased with experimental time. Structural modifications of the cells were visible after Lugol fixation only, indicating brittleness of the cell walls.P. micans has shown to be extremely sensitive to cadmium and to accumulate this metal.     

Carbon fixation and carbonic anhydrase activity in Haslea ostrearia (Bacillariophyceae) in relation to growth irradiance

The metabolic pathway of primary carbon fixation was studied in a peculiar pennate marine diatom, Haslea ostrearia (Bory) Simonsen, which synthesizes and accumulates a blue pigment known as “marennine”. Cells were cultured in a semi-continuous mode under saturating [350 μmol(photon) m⁻² s⁻¹] or non-saturating [25 μmol(photon) m⁻² s⁻¹] irradiance producing “blue” (BC) and “green” (GC) cells, characterized by high and low marennine accumulation, respectively. Growth, pigment contents (chlorophyll a and marennine), ¹⁴C accumulation in the metabolites, and the carbonic anhydrase (CA) activity of the cells were determined during the exponential growth phase. Growth rate and marennine content were closely linked to irradiance during growth: higher irradiance increased both growth rate and marennine content. On the other hand, the Chl a concentration was lower under saturating irradiance. The distribution between the Calvin-Benson (C₃) and β-carboxylation (C₄) pathways was very different depending on the irradiance during growth. Metabolites of the C₃ cycle contained about 70 % of the total fixed radioactivity after 60 s of incorporation into cells cultured under the non-saturating irradiance (GC), but only 47 % under saturating irradiance (BC). At the same time, carbon fixation by β-carboxylation was 24 % in GC versus about 41 % in BC, becoming equal to that in the C₃ fixation pathway in the latter. Internal CA activity remained constant, but the periplasmic CA activity was higher under low than high irradiance.     

Spatial variations of size-fractionated Chlorophyll, Cyanobacteria and Heterotrophic bacteria in the Central and Western Pacific

Geographic and vertical variations of size-fractionated (0.2–1μm, 1–10 μm, and >10 μm) Chlorophyll a (Chl.a) concentration, cyanobacteria abundance and heterotrophic bacteria abundance were investigated at 13 stations from 4^°S, 160^°W to 30^°N, 140^°E in November 1993. The results indicated a geographic distribution pattern of these parameters with instances of high values occurring in the equatorial region and offshore areas, and with instance of low values occurring in the oligotrophic regions where nutrients were almost undetectable. Cyanobacteria showed the highest geographic variation(ranging from 27×10³ to 16,582×10³cell l^-1), followed by Chl.a (ranging from 0.048 to 0.178μg l^-1), and heterotrophic bacteria (ranging from2.84×10³ to 6.50 ×10⁵ cell l^-1). Positive correlations were observed between nutrients and Chl.a abundance. Correspondences of cyanobacteria and heterotrophic bacteria abundances to nutrients were less significant than that of Chl.a. The total Chl.a was accounted for 1.0–30.9%, 35.9–53.7%, and 28.1–57.3% by the >10μm, 1–10 μm and 0.2–1 μm fractions respectively. Correlation between size-fractionated Chl.a and nutrients suggest that the larger the cell size, the more nutrient-dependent growth and production of the organism. The ratio of pheophytin to chlorophyll implys that more than half of the >10 μm and about one third of the 1–10 μm pigment-containing particles in the oligotrophic region were non-living fragments, while most of the 1–10 μm fraction was living cells. In the depth profiles, cyanobacteria were distributed mainly in the surface layer, whereas heterotrophic bacteria were abundant from surface to below the euphotic zone. Chl.a peaked at the surface layer (0–20 m) in the equatorial area and at the nitracline (75–100 m) in the oligotrophic regions. Cyanobacteria were not the principle component of the picoplankton. The carbon biomass ratio of heterotroph to phytoplankton was greater than 1 in the eutrophic area and lower than 1 in oligotrophic waters. This revised version was published online in August 2006 with corrections to the Cover Date.     

Photosynthetic characteristics of Dunaliella salina (Chlorophyceae,Dunaliellales) in relation to β-carotene content

Photosynthetic characteristics of Dunaliella salina with high (red form) and low β-carotene (green form) concentrations were studied. D. salina growing in brine saltworks exhibited a high level of β-carotene (15 pg cell⁻¹). The rate of oxygen evolution as a function of irradiance was higher in the red than in the green form (on chlorophyll basis). Photosynthetic inhibition of the green form was observed above 500 μmol m⁻² s⁻¹. The red form appeared more resistant to high irradiance and no inhibition in O₂ evolution was observed up 2000 μmol m⁻² s⁻¹. However, when these results are expressed on a cell number basis the rate of oxygen evolution was significantly higher in the green form. Carbonic anhydrase (CA) activity (total, soluble, membrane bound) was found in red and green forms. CA was higher in the red form on a chlorophyll basis, but lower if expressed on a protein basis. The light dependent rate of oxygen evolution and photoinhibition depends on the concentration of β-carotene in D. salina cells.     

Micropropagation of adult Swainsona formosa (Leguminosae: Papilionoideae: Galegeae)

Summary Explants of axillary buds excised from mature adult stems of Swainsona formosa (G. Don) J. Thompson (syn. Clianthus formosus) were cultured on Murashige and Skoog medium supplemented with a range of auxins, cytokinins, and sucrose concentrations. Auxins did not increase shoot or bud numbers above controls, and 2,4-dichlorophenoxyacetic acid was the only auxin to significantly increase callus production. Benzyladenine or thidiazuron incorporated into the medium at 0.1 μM stimulated shoot and bud production, and shoot growth occurred following removal of cytokinins from the medium after 4 wk. Shoot number increased linearly with sucrose concentration up to 40 g l⁻¹, but shoot height and the number of cytokinin-induced buds were optimal at sucrose levels of 20–30 g l⁻¹. Roots were initiated in vitro following treatment of cuttings with 0.1% indole-3-butyric acid and 0.1% α-naphthaleneactic acid. Plantlets were successfully established in soil but were plagiotropic and exhibited distichous phyllotaxy.     

Lake Muzahi,Rwanda: limnological features and phytoplankton production

Lake Muhazi, a small lake of Rwanda (East Africa) was studied from 1986 to 1990. A dramatic decrease of the catch of Oreochromis niloticus (350 T y⁻¹ in the fifties vs 30 T y⁻¹ in 1982) suggested a loss of productivity or overfishing. In the same period, other ecological changes occurred: the submerged macrophytes regressed and there was a decrease in Secchi depth (0.65 m in 1987 vs 1.5 m in the fifties). Compared to other lakes of the same area, the plankton production seemed low. The results of the present study characterize lake Muhazi as a shallow lake with a rather unstable diurnal stratification and with slight differences in mixing regime between its eastern, deepest part and its western, shallowest part. Secchi disk depth does not vary seasonally to a large extent. The water has a rather high mineral content (conductivity of about 500 μS cm⁻¹ at 25 °C) and low concentrations of dissolved N and P, except in the hypolimnion, where NH _inf4 ^sup+ -N can be high. Two species, Microcystis aeruginosa and Ceratium hirundinella, account for most of the phytoplankton biomass, which is about 50–80 mg chlorophyll a m⁻² in the euphotic zone, usually with little seasonal variation. Daily gross production estimates amount to about 6 to 9.5 g O₂ m⁻² d⁻¹ with a significant difference between the two parts of the lake. Data on C:N and C:P ratio in the phytoplankton suggest that some N deficiency might occur in the eastern part. Moreover, the Zm:Zc ratio could also lead to rather low net production rates (0.21–0.25 d⁻¹ for a mixed layer of 4 m) In conclusion, the primary production of lake Muhazi is medium for African lakes and the hypothesis that decreased planktonic production could account for a reduced fish production should be discarded. Whereas the present yield of the fishery is only 20 kg ha⁻¹ y⁻¹, the yield estimated from primary production ranges between 46 and 64 kg ha⁻¹ y⁻¹. This could be reached through proper management. Finally, some hypotheses are given to explain the ecological changes which occurred in the lake.     

Serum α-tocopherol and selenium in belgian infants and children

Previous studies showed low selenium (Se) concentrations in Belgian children. Serum α-tocopherol, retinol, total cholesterol, high-density lipoprotein and low-density lipoprotein cholesterol, selenium (Se), and thiobarbituric acid-reactive substances were examined. In order to obtain further information on the Se status in Belgian children, Se, α-tocopherol, retinol, and lipid concentrations were examined and signs of peroxidative lipid damage were evaluated in a subgroup. The study was performed in 524 children (0–14 yr old) during vaccination campaigns. Three age groups were analyzed: 0–1, 1–4, and 4–14 yr. In 87 of them, where sufficient amounts of serum were available, analysis of thiobarbituric acid-reactive substances was done. Infants have high serum α-tocopherol concentrations: (23.2 μmol/L [median and interquartile range: 18.6–30.2]) and low Se concentrations (0.37 mol/L [0.27–0.47]). Se concentrations rise significantly during the first 4 yr (p < 0.0001) (Mann-Whitney U-test, tied p-values): 0.70 μmol/L (0.59–0.82); in the 4–14 yr olds, it was 0.75 μmol/L (0.67–0.86). These values remain low compared to results coming from other parts of the world. α-Tocopherol concentrations decrease significantly after infancy (p < 0.0001). The ratio α-tocopherol/total cholesterol is higher in infants. This is induced by the high vitamin E content of infant formulas. Signs of serum lipid peroxidation could not be detected by analysis of serum malondialdehyde concentrations. High α-tocopherol concentrations, as those observed in infant serum lipids, could be one of the protective mechanisms from the peroxidative lipid damages, sometimes observed in a low-Se status.     

Bacterial utilization of algal extracellular products in a southwestern reservoir

Rates of carbon flow from phytoplankton to bacteria were estimated for Lake Arlington, Texas. The lake is a warm (annual temperature range 7 to 35 °C), shallow, monomictic reservoir with limited macrophyte development in the littoral zone. Samples were collected from 6 depths within the photic zone from a site located over the deepest portion of the lake. Primary production and exudate production were calculated from NaH¹⁴CO₃ incorporation. Bacterial production was calculated from [methyl-³H]-thymidine incorporation. Depth averaged primary production ranged from a seasonal low of 9.0 μg C l⁻¹ h⁻¹ in January to a seasonal maximum of 153 μg C l⁻¹ h⁻¹ during holomixis in September. Annual depth-averaged production was 67.8 ± 7.3 μg C l⁻¹ h⁻¹. Exudate production ranged between 21.9 and 54.2% of primary production and annually averaged 30.8%. Bacterial production ranged between 1.7 and 46.0 μg C l⁻¹ h⁻¹ and annually averaged 16.0 ± 1.9 μg C l⁻¹ h⁻¹. Bacteria processed approximately 70% of exudate and incorporated 35% into biomass. Bacterial production was positively correlated with total primary production (r = 0.38, p < 0.003, n = 6), particulate primary production (r = 0.34, p < 0.004, n = 70) and bacterial uptake of exudate (r = 0.43, p < 0.001, n = 68). While exudate was readily utilized by bacteria it dit not appear to be produced in sufficient quantity or at a sufficient rate to serve as the sole or a major source of carbon supporting bacterial growth.     

Seasonal and spatial distribution of bacterial production and biomass along a salinity gradient (Northern Adriatic Sea)

The Adriatic Sea is a semi-enclosed ecosystem that receives in itsshallow part, the northern basin, significant freshwater inputs whichmarkedly increase its productivity with respect to the oligotrophic featuresof the Mediterranean sea. In this area, especially on the western coastwhere river plumes diffuse, high physical (density) and chemical (nutrients)gradients occur on a small scale, both horizontal and vertical. Results ofbacterial production as ³H-thymidine incorporation, bacterialabundance as DAPI direct count, autotrophic biomass as chlorophyll a andtotal biomass as ATP from three areas in the Northern Adriatic Sea arereported. The three sites, differently influenced by the river waterdiffusion, were sampled seasonally over two days, every 24 h, in foursurveys from April 1995 to January 1996. Bacterioplankton production,strongly correlated with primary production, was extremely high near thecoast in low-salinity, high-nutrient waters, mostly as an indirectconsequence of riverine inputs causing an increase in phytoplanktonproduction stimulated by physically driven nutrient inputs. In the warmmonths bacterial activity was higher than in cold months. While bacteriaabundance did not appear related to the salinity gradients, bacterialproduction (from 0.6 to 372 pM ³H-thymidine h^™1incorporated, corresponding to 0.01–8.2 μg C l^™1h^™1) and the relative generation times (from 0.2 to 35 days)showed a high range of values, representing a variety of situations, fromestuaries to the ocean. The resulting role of the bacterial community in thecarbon cycle is very consistent, processing amounts of carbon which havebeen estimated as high as the 80% and the 260% of thosesynthesized by autotrophs in summer and winter, respectively. This revised version was published online in July 2006 with corrections to the Cover Date.     

Short Communication—Effects of oligosaccharins on callus growth and saponin content of Panax notoginseng

This work provides some evidences for the saponin production of Panax notoginseng callus by using biologically active,wall-related oligosaccharins.In an appropriate concentration,three kinds of oligosaccharins stimulated saponin formation of callus growth.The concentration of DO,GO and CO for saponin production of Panax notoqinseng callus culture were 15ppm,15ppm aud 20ppm respectively by comparing saponin yield,It was very obvious for DO to increase saponin content when the concentration was 10ppm,and for GO to stimulate callus growth when the concentration was 20ppm,It would be a good way to produce sapoin by using oligosaccharins in large scale culture in the future.     

Size-fractionated biomass and productivity of phytoplankton and particulate organic carbon in the southern ocean

During the austral summer of 1989/1990, surface samples were obtained of size-fractionated biomass, and the productivity of phytoplankton, its cell abundance, the composition of the dominant species, the concentration of particulate organic carbon (POC) and the related environmental surface parameters were measured in a large-scale survey primarily of the Atlantic and Indian Sectors. The results showed that the southern atlantic sector is the most fertile; chlorophylla (Chla) concentration averaged over 2 μg l⁻¹, average cell abundance was about 41.0 × 10³ cell l⁻¹, and average POC concentration was also the highest (>100 μg l⁻¹), but was lower in the Drake Passage and the southern Indian sector. The results for size-fractionated Chla showed that netplankton (>20 μm) in the South Atlantic Ocean, having abundant nutrients, accounted for the highest proportion (average 65%) of biomass. In the infertile South Indian Ocean, picoplankton (<2 μm) accounted for the highest proportion, averaging 47%. The results for size-fractionated productivity showed that the contribution of picoplankton to total productivity was the largest in the South Atlantic Ocean and Drake Passage, those of nanoplankton (2–20 μm) and netplankton being about equal. The relatively high photosynthesis assimilation number of picoplankton demonstrates their importance in the marine ecosystems of Antarctic water. In comparison with the Antarctic water, the subantarctic and subtropical waters are infertile.     

Site-specific biotinylation of human myeloid differentiation protein 88 in <Emphasis Type="Italic">Drosophila melanogaster</Emphasis> Schneider 2 cell cytoplasm

In this work we describe the production of site-specific biotinylated human myeloid differentiation factor 88 (MyD88). A vector containing a coding sequence for a peptide derived from the carboxyl terminus of the Klebsiella pneumoniae oxalacetate decarboxylase α subunit was used to allow expression and biotinylation of MyD88 in Drosophila melanogaster Schneider 2 cell cytoplasm. As estimated by a comparison of Schneider 2 lysate with standard protein, the maximum expression level was 1.3 μg 10⁷ cells⁻¹. About 4 mg of biotinylated protein was purified by affinity chromatography on monomeric avidin from a I-L culture. Exogenous biotin added to the culture medium increased the biotinylation efficiency of the expressed protein. Biotinylated MyD88 produced in Drosophila cells was able to precipitate recombinant MyD88 expressed in human embryonic kidney cells. The stable expression of MyD88 in Drosophila Schneider 2 cells offers a convenient and attractive method for large-scale production, which may be required to clarify the role of MyD88 in the inflammatory response. Moreover, site-specific biotinylation of MyD88 provides a useful tag for interaction assays where high sensitivity is required.     

Somatic embryogenesis of Gentiana genus III. Characterization of three-year-old embryogenic suspensions of G. pannonica originated from various seedling explants

Experiments were carried out with three-year-old embryogenic suspension culture of Gentiana pannonica Scop. The initial explant for the suspension determinated both the embryogenic character and embryo production. Cultures were initiated by culture of hypocotyl, cotyledon and root explants on MS (Murashige and Skoog 1962) medium supplemented with 1.0 mg·l⁻¹ Kinetin and 0.5 mg·l⁻¹ 2,4-D, later transferred and maintained in liquid MS medium with 1.0 mg·l⁻¹ Dicamba, 0.1 mg·l⁻¹ NAA, 2.0 mg·l⁻¹ BAP and 80.0 mg·l⁻¹ AS. Regeneration medium included 0.0–1.0 mg·l⁻¹ GA₃+0.0−2.0 mg·l⁻¹ Kin.+0.0−160 mg·l⁻¹ AS. In these culture conditions, the effect of the explant was found to be the most important factor. The curve of growth, growth coefficient and % of participation of various size aggregates differed in the studied suspensions. Flow cytometry revealed various DNA content in nuclei from praembryogenic mass depending on the explant origin. To complete embryogenesis the medium was changed from liquid to solidified in the presence of the same plant growth regulators combination required. The most embryogenic culture appeared hypocotyl-derived and it yielded the highest number of somatic embryos. The suspension culture originating from root proliferated the highest number of embryogenic cell clusters but did not produce embryos for fraction 120–450 μm. One hundred mg of suspension of the fraction that was larger than 450 μm yielded 309, 175, 123 embryos for the following suspensions: root-, cotyledon-, hypocotyl-derived, respectively. Almost 50 % of non-deformed fully developed embryos from all studied suspensions passed conversion into germling stage and finally plants were regenerated.     

The impact of ozone fumigation and fertilization on chlorophyll fluorescence of birch leaves (Betula pendula)

 The impact of ozone fumigation on chlorophyll a fluorescence parameters and chlorophyll content of birch trees grown at high and low fertilization were studied for 6-, 8-, and 12-week old leaves. Fluorescence parameters were measured with a portable fluorometer with its fibre optics tightly inserted in a gas exchange cuvette at light intensities from 0 to 220 μmol photons m⁻² s⁻¹. Ozone caused significant changes of primary photosynthetic reactions: a decrease of the quantum yield of photosystem II and an increase of non-photochemical quenching. In all leaves a biphasic light response of non-photochemical quenching was observed. Ozone fumigation shifted the onset of the second phase from a PFD of about 60 μmol m⁻² s⁻¹ to about 30 μmol m⁻² s⁻¹. While the fertilizer concentration had no influence on this character, high fertilization supply of plants partially reduced O₃-induced damage. The light responses of Ft, Fm′ and NPQ observed in birch leaves grown in O₃-free air indicate the existence of at least two different processes governing energy conversion of the photosynthetic apparatus at PS II in the range of PFD 0–200 μmol photons m⁻² s⁻¹. The first phase was attributed to a rather slowly relaxing type of non-photochemical quenching, which, at least at low PFD, is thought to be related to a state 1–2 transition. The further changes of the fluorescence parameters studied at higher PFD might be explained by an increase of energy-dependent quenching, connected with the energization of the thylakoid membrane and zeaxanthin synthesis. A major effect of ozone treatment was a lowering of PS II quantum yield. This reflects a reduction of PS II electron transport and corresponds to the reduction of CO₂-fixation observed in ozonated leaves. Received: 24 September 1996 / Accepted: 27 January 1999