Effect of Inorganic Phosphate on the Biosynthesis of Purine and Pyrimidine Nucleotides in Suspension-Cultured Cells of Catharanthus roseus

The levels of purine and pyrimidine nucleotides in suspensioncultures of Catharanthus roseus were determined 24 h after stationary-phasecells were transferred to fresh complete (‘+Pi’)or phosphate-deficient (‘–Pi’) Murashige-Skoogmedium. The levels of ATP, GTP, UTP and CTP were from approx.3 to 5-fold greater in the cells grown in ‘+Pi’medium than in the cells grown in ‘–Pi’ medium.The levels of almost all other nucleotides were slightly higherin the cells in ‘+Pi’ medium. The rates of de novoand salvage biosynthesis of purine and pyrimidine nucleotideswere estimated from the rates of incorporation of radioactivityfrom [¹⁴C]formate, [2–¹⁴C]glycine, NaH¹⁴CO₃, [6–¹⁴C]orotate,[8–¹⁴C]adenine, [8–¹⁴C]adenosine, [2–¹⁴C]uraciland [2–¹⁴C]uridine. The results indicated that the activityof both the de novo and the salvage pathway was higher in thecells in ‘+Pi’ medium than in the cells in ‘–Pi’medium. The rate of degradation estimated from the rate of releaseof ¹⁴CO₂ from labelled purines and pyrimidines indicated thatdegradation of uridine was significantly reduced in the cellsin ‘+Pi’ medium, but no significant difference wasfound in the degradation of adenine, adenosine and uracil. Thepossible role of Pi in the control of the biosynthesis of nucleotidesand in the degradation of uridine is discussed. Catharanthus roseus, Madagascar periwinkle, suspension culture, inorganic phosphate, nucleotides, purines, pyrimidines, biosynthesis, degradation     

Salt Stress Causes Acceleration of Purine Catabolism and Inhibition of Pyrimidine Salvage in Zea mays Root Tips

Nucleotide metabolism was studied in apical 5.0 mm root tipsof corn plants (Zea mays L., cv. Pioneer 3906) hydroponicallycultured for 7 d and then salinized for 19 d at a rate calculatedto reduce the osmotic potential (_o) of the solutions by O.1MPad^–1 to a final _o = -0.4 MPa. Saline treatments withtwo different molar ratios of Ca₂₊/Na⁺ were employed, viz.,0–03 (2.5 mol m^–3 CaCl₂ + 86.5 mol m^–3 NaCl)for the NaCl treatment and 0.73 (31.5 mol m^–3 CaCl₂ +43.1 mol m^–3 NaCl) for the NaCl + CaCl₂ treatment. Bothsalt treatments reduced root growth by more than 30%. The capacityof roots to provide purine nucleotides either by de novo synthesisor by re-utilization of existing bases, e.g. salvage of hypoxanthineto adenine nucleotides, was not affected by either salt treatment.However, catabolism of hypoxanthine was accelerated more than3.5-fold by both salt treatments, demonstrating an increasedcapacity for purine catabolism which would shift the normal1: 1 ratio of synthesis: degradation of purine nucleotides observedfor the roots of healthy control plants to less than 0.2 duringsalt stress. The ratio of pyrimidine nucleotide synthesis: degradationwas also reduced. In this case, the unfavourable shift towardnucleotide degradation resulted because both salt treatmentsreduced salvage capacity by more than 25%, but had no compensatingeffect on de novo synthesis or catabolism of pyrimidines. Key words: Salinity, osmotic potential, nucleotide metabolism     

Response of marine phytoplankton to low levels of arsenate

Phytoplankton species vary widely in their degree of inhibitionto low levels of dissolved arsenate (1 – 10 ? ambient).Similarly, natural phytoplankton assemblages cultivated outdoorsunder ambient temperature and nutrient conditions indicate thatthe observed variance in sensitivity is sufficient to causea marked change in species composition and succession in dosedassemblages relative to controls, again at very low levels ofarsenate. The changes in species that occurred, however, werenot always similar to the response predicted from single–speciescultures. In addition, a species' level of resistance to arsenateis often not comparable with its resistance to other anthropogenicstress. It is therefore questionable whether predictions concerningenvironmental consequences of a given pollutant can be madeon the basis of laboratory bioassays of a single species. ¹Contribution # 4695 Woods Hole Oceanographic Institution ²Present address: Academy of Natural Sciences, Division of EnvironmentalResearch, Benedict Estuarine Research Laboratory, Benedict,MD 20612, USA     

Floodwater Oxygen Content, Ethylene Production and Lenticel Hypertrophy in Flooded Mango (Mangifera indica L.) Trees

A system was developed to test the effects of floodwater O₂concentration on ethylene evolution and stem lenticel hypertrophy,and the effects of exogenous ethylene on stem lenticel hypertrophyin mango (Mangifera indica L.) trees. Dissolved O₂ concentrationsof 1–7x10^–9 m³ m^–3 generally resulted in hypertrophyof stem lenticels within about 6 d of flooding, whereas floodwaterO₂ concentrations of 13–15 x 10^–9 m³ m^–3 delayedhypertrophy until about day 9. After 14d of flooding, therewere more than twice the number of hypertrophied lenticels pertree with floodwater O₂ concentrations of 1–7 x 10^–9m³ m^–3 than with floodwater O₂ concentrations of 15 x10^–9 m³ m^–3. Ethylene evolution from stem tissueimmediately above the floodline increased 4- to 8-fold in treesexposed to floodwater O₂ concentrations of 1–2 x 10^–9m³ m^–3, increased 2-fold for trees exposed to floodwaterO₂ concentrations of 6–7 x 10^–9 m³ m^–3, butremained constant with floodwater O₂ concentrations of 13–15x 10^–9 m³ m^–3. Plants maintained in highly oxygenatedfloodwater (13–15 x 10^–9 m³ m^–3), and givenexogenous ethylene developed many hypertrophied lenticels, whereasplants in highly oxygenated water and not given ethylene developedfewer or nohypertrophied lenticels. These data suggest thatethylene plays a role in promotion of stem lenticel hypertrophyin flooded mango trees, and that floodwater dissolved oxygenconcentration can regulate stem lenticel hypertrophy and ethyleneevolution in this species. Key words: Flooding, hypoxia, hypertrophic cell swelling     

Regeneration of Shoots on Root Explants of Flax

Regeneration of shoots from adventitious root explants of flaxwas achieved for two of five cultivars tested. Root explantsof the cultivar Bombay regenerated buds on MS medium with varioussupplements, the best combination being 002 mg I^–1 NAA,1 mg I^– 6-BA, 20 mg I^– adenine and 500 mg I^–cefotaxime. Adenine, in the presence of 6-BA, and cefotaxime,in the presence of both 6-BA and adenine, were found to stimulatebud initiation, but the most important factor influencing budregeneration from flax roots was genotype     

The Occurrence of Nitrate Reduction in the Leaves of Woody Plants

Nitrate reductase activities greater than 02 µmol h^–1g^–1 f. wt, measured by an in vivo assay, occurred in 41per cent of a large sample (555 species) of woody plants. Ifseveral taxonomic groups (Gymnosperms, Ericaceae and Proteaceae)with consistently low activities were discounted activitiesgreater than 02 µmol h^–1 g^–1 f. wt occurredin 73 per cent of the species. This compares with 93 per centin herbaceous species, suggesting that leaf nitrate reductionis of common occurrence in woody plants. In a small sample ofspecies leaf nitrate reductase activity correlated with nitrateconcentration in the xylem sap. Low activities occurred consistentlyin the Gymnosperms, Ericaceae and Proteaceae. Feeding cut shootsof representatives of these groups with nitrate caused inductionof leaf nitrate reductase activity in the Gymnosperms and Proteaceae,but only limited induction in the Ericaceae. The Ericaceae,with the exception of two species, had low activities and lownitrate reductase inducibility. Root assimilation may predominatein the Gymnosperms and Proteaceae. It is suggested that nitratereduction generally occurs in the leaves of trees from a varietyof plant communities and that this may be related to the lowerenergy cost of leaf, as opposed to root, nitrate assimilation. Nitrate reductase, trees and shrubs, leaves, nitrate assimilation, nitrate translocation, nitrate reductase induction, energy cost, plant ecology     

The Relationship between Sucrose and Starch during 'Dark' Export from Leaves of Uniculm Barley

Uniculm barley plants were grown in 8 h photoperiods at a quantumflux density of 655 µE m^–2 s^–1. Groups ofplants were transferred to four different light environmentsfor one 8 h photoperiod (106, 270, 665, and 975 µE m^–2s^–1) and harvested at intervals throughout the succeedingdark period for subsequent carbohydrate analysis of the youngestmature leaf. Sucrose was the predominant carbohydrate in the leaves (attaininga level of c. 100 mg dm^–2 after 8 h at 975 µE m^–2s^–1) but starch was also of significance (20 mg dm^–2after 8 h at 975 µE m^–2 s^–1). During the dark period, following a photoperiod at the threehighest light levels (270, 665, and 975 µE m^–2 s^–1),sucrose was exported first while the starch level remained fairlyconstant. When the-sucrose level fell to 15–20 mg dm^–2starch degradation began. This critical sucrose level was reachedearlier in those plants subjected to lower quantum flux densitiesduring the preceding photoperiod. The delay in the remobilizationof starch suggests an important regulatory mechanism which maybe dependent upon the sucrose level. At 106 µE m^–2s^–1 the sucrose level rose to only 10 mg dm^–2. Herethere was no discernible delay in the depletion of sucrose orstarch.     

Structure and Function of an Age Series of Eucalypt Plantations in Central Himalaya. I. Dry Matter Dynamics

The biomass and net primary productivity (NPP) of 2- to 8-year-oldplantations of Eucalyptus tereticornis Sm. (= E. hybrid) growingin the tarai (a level area of superabundant water) region ofCentral Himalaya were estimated. Allometric equations for allthe above-ground and below-ground components of trees and shrubswere developed for each stand. Understorey, forest floor biomassand litter fall were also estimated from stands. Shrubs appearedfirst at 5-year-old plantation. The biomass of vegetation, forestfloor littermass, tree litter fall and net primary productivity(NPP) of trees and shrubs increased with the increase in plantationage, whereas herb biomass and NPP significantly (P < 0·01)decreased with the increase in plantation age. The total plantationbiomass increased from 7·7 t ha^–1 in the 2-year-oldto 126·7 t ha^–1 in the 8-year-old plantation andNPP from 8·6 t ha^–1 year^–1 in the 2-year-oldto 23·4 t ha^–1 year^–1 in the 8-year-old plantation.The biomass accumulation ratio ranged from 0·81 to 5·93. Eucalyptus tereticornis Sm, plantation, biomass, forest floor, litter fall, net primary productivity, biomass accumulation ratio     

Micropropagation of Pissardi Plum

An efficient medium for multiplication of Prunus cerasifera,J. F. Ehrh. cv. ‘Atropurpurea’, Pissardi plum, consistedof Linsmaier-Skoog basal medium (LS) supplemented with 3% sucrose,10mg 1^–1 N⁴-(²-isopentenyl) adenine (2iP), and 162 mg1^–1 phloroglucinol (Phl). Phl in the medium significantlyenhanced growth (P < 0.1 %) over cultures maintained on LSmedium with 10 mg 1^–1 2iP and no Phl. Plantlets were rootedon a half-strength Murashige-Skoog (MS) medium supplementedwith 0.2 mg 1^–1 indole-3-butyric acid (IBA). Prunus cerasifera, Pissardi plum, micropropagation, phloroglucinol, N⁶-(²-isopentenyl) adenine     

The Structure and Function of Pine Forest in Central Himalaya. I. Dry Matter Dynamics

The present study deals with structure and function of fourareas of Himalayan chir pine forest. Tree layer was monospecificon all sites with varied density and basal cover in the rangeof 540–1630 individuals per ha and 25·0–47·2m²ha^–1, respectively. Shrubs having low density were sparselydistributed. All allometric equations relating to biomass ofdifferent components, to circumference at breast height (cbh)were significant, with the exception of that for cone biomass.Total vegetation biomass (115–236 t ha^–1) was distributedas 113–283 t ha^–1 in trees. 0·56–0·82t ha^–1 in shrubs and 1·63–2·57 t ha^–1in herbs. Total forest floor biomass including herbaceous litterranged between 9·6 and 13·6 t ha^–1. Of thetotal annual litter fall (4·26–7·38 t ha^–1),60·3–75·1 per cent was distributed in leaflitter and 24·9–39·7 per cent in wood litter.Turnover rate of tree litter varied from 0·45 to 0·53,whereas rates for shrubs and herbs were assumed to 1. Net primaryproduction of total vegetation ranged between 9·91 and21·2 t ha^–1 year^–1, of which the contributionof trees, shrubs and herbs was 76·5– 88·1per cent 0·6–1·8 per cent and 11·3–21·5per cent, respectively. A compartment model of dry matter onthe basis of mean data across sites was developed to show drymatter storage and flow of dry matter within the ecosystem. Pinus roxburghii forest, biomass, litter fall, net primary production, compartmental transfer     

Photosynthesis in Panicum milioides, a Species with Reduced Photorespiration

The capacity for C₄ photosynthesis in Panicum milioides, a specieshaving reduced levels of photorespiration, was investigatedby examining the activity of certain key enzymes of the C₄ pathwayand by pulse-chase experiments with ¹⁴CO₂. The ATP$P₁ dependentactivity of pyruvate,P₁ dikinase in the species was extremelylow (0.14–0.18 µmol mg chlorophyll^–1 min^–1).Low activity of the enzyme was also found in Panicum decipiensand Panicum hians (related species with reduced photorespiration)and in Panicum laxum (a C₃ species). The antibody to pyruvate,P₁dikinase caused about 70% inhibition of the ATP$P₁ dependentactivity of the enzyme in P. milioides. The activity of NAD-malicenzyme and NADP-malic enzyme in ^P. ^milioides was equally low(approximately 0.1–0.2 µmol mg chlorophyll^–1min^–1) and similar to the activity in P. decipiens, P.hians and P. laxum. Photosynthetic pulse-chase experiments underatmospheric conditions showed a typical C₃-like pattern of carbonassimilation including the labelling of glycine and serine asexpected during photorespiration. During the pulse with ¹⁴CO₂only about 1% of the labelled products appeared in malate and2–3% in aspartate. During a chase in atmospheric levelsof CO₂ for up to 6 min there was a slight increase in labellingin the C₄ acids. The amount of label in carbon 4 of aspartatedid not change during the chase, indicating little or no turnoverof the C₄ acid via decarboxylation. The results indicate thatunder atmospheric conditions P. milioides assimilates carbondirectly through the C₃ pathway. Photorespiration as indicatedby the CO₂ compensation point may be repressed in the speciesby a more efficient recycling of photorespired CO₂. (Received June 8, 1982; Accepted July 22, 1982)     

Feeding, growth and food conversion of the marine cladoceran Penilia avirostris

Ingestion and clearance rates, feeding behaviors and life historyvariables of the marine cladoceran Penilia avirostris were evaluatedover a range of food concentrations encountered in nature (0.01–3.0mm³ 1^–1 of Isochrysis galbana). Ingestion rates increasedand clearance rates decreased with increasing food concentration.No maximum feeding thresholds were observed over the range ofalgal concentrations offered. Weight-specific ingestion ratesdecreased with increasing body weight. Feeding behaviors suchas mandibular activity, abdominal claw rejections of cloggedfeeding structures and feeding appendage activity decreasedat a food level of 0.3 mm³ l^–1 of l. galbana. Peniliaavirostris had very poor survivorship at extremely low (0.01mm³ l^–1 and high (3.00 mm³ l^–1) food levels. Mortalitywas hardly affected at food levels of 0.03–1.0 mm³ l^–1Reproduction did not occur at food levels of     

Acid Phosphatase Activity in Karri (Eucalyptus diversicolor F. Muell.) in Relation to Soil Phosphate and Nitrogen Supply

O'Connell, A. M. and Grove, T. S. 1985. Acid phosphatase activityin karri (Eucalyptus diversicolor F. Muell.) in relation tosoil phosphate and nitrogen supply.—J. exp. Bot. 36: 1359–1372 Soluble acid phosphatase activity was measured in tissues ofkarri (Eucalyptus diversicolor F. Muell.) seedlings and fiveyear old karri trees to which P and N fertilizer had been applied.Addition of P from 0 to 1250 mg P kg^–1 soil with a basaltreatment of other nutrients produced significant increasesin growth, P content and P concentration of karri seedlings.In each of five plant components (shoot tips, partly expandedleaves, mature leaves, young stems and old stems) soluble acidphosphatase activity was greatest at low levels of added P anddecreased with increasing soil P supply. The range of acid phosphataseactivity (0·5-6·5 µmol NPP g^–1 f.wt.min^–1) was similar to that reported for a number of agriculturaland horticultural plants. Enzyme activity was highest for shoottips and lowest for old stems. However, the relative changein activity with decreasing soil P supply was greatest for stems(4·3 fold) and least for shoot tips (2·7 fold) Mature leaves of seedlings grown in ‘high P’ and‘low P’ soil at four levels of added N showed, inaddition to the effect of P, a significant N-P interaction onsoluble acid phosphatase activity. In leaf samples from fiveyear old karri trees there was a significant decrease in solubleacid phosphatase with increasing P fertilization. Addition ofN fertilizer had no significant effect on enzyme activity, probablybecause added N had little effect on foliar N concentrations Exponential models relating (1) plant growth to enzyme activityand (2) plant growth to P concentration in stems and matureleaves of plants grown in soil with a range of added P accountedfor 78–92% and 63–87%, respectively, of the variationin top dry weight. The results suggest that for the diagnosisof plant P status, (1) stem components may be the most appropriatetissue to sample, and (2) nutrient and enzyme assays may complementeach other, P concentration being most useful where P supplyis adequate and phosphatase activity where P supply limits growth Key words: Phosphatase activity, Eucalyptus diversicolor, nutrients, phosphorus, nitrogen, forests     

Isoforms of NADP-dependent Malic Enzyme in Tissues of the Greening Maize Leaf

Scagliarini, S., Pupillo, P. and Valenti, V. 1988. Isoformsof NADP-dependent malic enzyme in tissues of the greening maizeleaf.—J. exp. Bot. 39: 1109–1119. The compartmentation of the isoforms of NADP-dependent malicenzyme (E.C. 1.1.1.40 [EC] ) has been studied in cell-free extractsand in enzymatically-isolated protoplasts of mesophyll tissue(MT) and bundle sheath (BS) strands of greening maize leaves.The etiolated leaf of 10-d-old seedlings contains a cytosolicisozyme with a pl of 5.4 ?0.1 at low specific activity (s.a,45 ? 3 nmol min^–1 mg^–1 protein), found both in MTand BS. The green leaf on the other hand contains the dominantBS chloroplast isozyme with pl 4.6 ? 0.2 at a s.a, of 370 ?40 nmol min^–1 mg^–1 protein (3.2 ? 0.5 µmolmin^–1 mg^–1 chl) and a minor, previously undescribedisoform with pl 6.5 ? 0.1 also localized in the BS at a s.a.of 38 ? 6 nmol min^–1 mg^–1 protein. Green MT protoplastshave only traces of pl 4.6 isozyme. After illumination of dark-grown seedlings, the total leaf activityshows a rapid increase (1.5-fold within 2 h), attributed mainlyto the pl 5.4 isozyme of MT protoplasts and BS strands. Thisis followed by a large increase of enzyme activity due to thecontinued rise of pl 5.4 isozyme for about 24 h and, after aninitial lag of a few hours, to the accumulation of pl 4.6 isozyme.After 18 h illumination, pl 4.6 and 5.4 isozyme activities tendto decline in the MT whereas they are still increasing in theBS, particularly the former. This pl 4.6 species has becomethe major one by 48 h illumination. The final pattern of greenleaves is established around 96 h light, when the chloroplastisozyme has attained its maximum level, the pl 5.4 isozyme ofBS strands has been superceded by the pl 6.5 species (also supposedto be cytosolic) and MT protoplasts retain little residual activity.Some metabolic implications of the changing pattern of NADP-dependentmalic isozymes during maize leaf greening are discussed. Key words: C₄, isozymes, malic enzyme, photodifferentiation, Zea mays     

The Kinetics of Tracheid Development in Tsuga canadensis Carr. and its Relation to Tree Vigour

Cell counts from samples taken at weekly intervals, from 14May to 22 October 1969, in a T. canadensis stand in Massachusetts,U.S.A., showed that the width of the annual ring was correlatedwith the rate of cell production and that only the least vigoroustrees (c. 20 tracheids year^–1) had a shorter growing season.The time required for completion of a cell-division cycle inthe cambial zone decreased during the course of the season,from 35 to 20 days for the less vigorous trees (25–45tracheids year^–1) and from 28 to 10 days for the morevigorous trees (45–100 tracheids year^–1). The timerequired for the completion of radial growth of the tracheidsdecreased from 18 to 9 days, with no evidence of any changeswith tree vigour. The actual radial growth-rate of the tracheidswas constant within the range 1.5–3 um day^–1. Thetime required for deposition of the secondary cell wall increasedfrom 10 to 50 days, with little evidence of any changes withtree vigour. The actual rate of deposition of cell wall materialwas about 0.15 µ² µ^–1 day^–1 and seemedto show little change during the course of the season. The timeperiod required for lysis of the cytoplasm was about 4 days,with no evidence of any changes with tree vigour and littleevidence of any changes during the course of the season.     

Stimulatory Effect of Chloride Ions on NADP Malic Enzyme from Leaves of two C4 Species of Cyperus

NADP malic enzyme (EC 1.1.1.40 [EC] ) from leaves of two C₄ speciesof Cyperus (C. rotundus and C. brevifolius var leiolepis) exihibiteda low level of activity in an assay mixture that contained lowconcentrations of Cl^–. This low level of activity wasmarkedly enhanced by increases in the concentration of NaClup to 200 mM. Since the activity of NADP malic enzyme was inhibitedby Na₂SO₄ and stimulated by relatively high concentration ofTris-HCl (50–100 mM, pH 7–8), the activation ofthe enzyme by NaCl appears to be due to Cl^–. Variationsin the concentration of Mg²⁺ affected the K_A (the concentrationof activator giving half-maximal activation) for Cl^–,which decreased from 500 mM to 80 mM with increasing concentrationsof Mg²⁺ from 0.5 mM to 7 mM. The K_m for Mg²⁺ was decreased from7.7 mM to 1.3 mM with increases in the concentration of NaClfrom zero to 200 mM, although the increase of V_max was not remarkable.NADP malic enzyme from Cyperus, being similar to that from otherC₄ species, was able to utilize Mn²⁺. The K_m for Mn²⁺ was 5mM, a value similar to that for Mg²⁺. The addition of 91 mMNaCl markedly decreased the K_m for Mn²⁺ to 20 +M. NADP malicenzyme from Setaria glauca, which contains rather less Cl^–than other C₄ species, was inactivated by concentrations ofNaCl above 20 mM, although slight activation of the enzyme wasobserved at low concentrations of NaCl at pH7.6. (Received February 20, 1989; Accepted June 12, 1989)     

Quantitative Aspects of Leaf Acid Phosphatase Activity and the Phosphorus Status of Tomato Plants

The relation between tomato leaf acid phosphatase activity andleaf tissue P content has been examined, and a study made ofthe effects of leaf development, variation in nitrogen supply,and variation in the growing medium on this relationship. Tomatoplants were grown in sand and given various concentrations ofphosphate. Plants were also grown for an initial period in peatcontaining an adequate level of phosphate, then transferredto peat to which was added 0 or 2.3 kg superphosphate m^–3and supplied with either 50 of 300 µg N ml^–1. Expressed on a unit tissue f. wt basis, acid phosphatase activityin the control plants in sand (given 41 µg P ml^minus;1)was highest in extracts from the expanding leaves and decreasedwith leaf maturity. However, when given a reduced supply ofphosphate, the enzyme activity in the more mature leaves wasequal to, or greater than, that in the expanding leaves. Thephosphatase activity increased first in the young, fully-expandedleaves and in the mature leaves (with 4.1 µg P ml^–1),but did not increase in the expanding leaves until the supplywas restricted to 2.1 µg P ml^–1. On closer examination,the increase in enzyme activity appeared to be associated withthe P level in the leaf tissues, the activity increasing whenthe level fell below about 0.25 per cent (g P per 100 g drywt tissue). The same relation was found with the plants grownin peat, and was independent of the concentration of nitrogensupplied to the plants. The fully expanded leaves showed the best enzyme response whenthe phosphate supply was restricted and the activity reflectedclosely the local levels of tissue P. The assay of the enzymein unpurified leaf extracts is simple and rapid, and could beused in a test to detect P-deficiency in tomato plants. Lycopersicon esculentum L, tomato, acid phosphatase activity, phosphorus status     

The plankton of a large oligotrophic freshwater Antarctic lake

The planktonic community of Crooked Lake, a large freshwaterlake in the Vestfold Hills, Antarctica was investigated duringthe austral summer in 1990. Very low levels of chlorophyll aranging between mean values of 0 29 and 1.8 µl^–1were recorded. The phytoplankton was largely made up of colouredflagellates, including single species of Chlamydomonas, Ochromonasand Pendimum, which occurred in low concentrations (23.8x 10²–47.3x10² l^–1). Heterotrophic colourless flagellates, includingParaphysomonas vestita, were also relatively sparse (2.1x 10²–21.3x10²l^–1). Ciliated protozoans were particularly poorly represented.Only three species occurred reaching densities of 1001^–1,and among them the mixotrophic species Strombidium vinde wasthe most common. A single species of heliozoan Actinosphaeriumand relatively large numbers of naked amoebae were the sarcodinerepresentatives The protistan community and the bacteria wereconcentrated into microbial consortia associated with floesof paniculate organic matter probably derived from the benthicalgal mat. Of the two microcrustacean zooplankters recordedfrom the lake only Daphniopsis studeri was found breeding inthe plankton in very low numbers. The behavioural and physiologicaladaptations of the organisms inhabiting this extremely oligotrophicenvironment are discussed.     

The Water Relations of Young Olive Trees in a Mediterranean Winter: Measurements of Evaporation from Leaves and Water Conduction in Wood

We report measurements of evaporation rate, leaf resistanceto evaporation and water conduction in the stems of young olivetrees (Olea europea L.) growing in Messina, Italy, during thewinter and early spring. We have measured what Zimmermann calls‘leaf specific conductivity’ (LSC) of stem segmentsexcised from olive trees. The LSC is a measure of the specifichydraulic conductivity of stem segments normalized per unitarea of leaves supplied by the stem segment rather than perunit area of sapwood cross-sectional area. We find that theLSC's of primary stems were the largest followed in magnitudeby the LSC's of secondary stems and tertiary stems. Under winterand early spring conditions the maximum evaporative flux fromCoratina and Nocellara varieties of olive trees is about 2.6x 10^–5 kg 8^–1 m^–2. From this and the LSC measurementswe calculate that the pressure gradients needed to maintainthis rate of evaporation in the steady state is 65 kPa m^–1in primary stems, 170 kPa m^–1 in secondary stems and 560kPa m^–1 in tertiary stems. Olive, Olea europea L, evaporation, leaf specific conductivity, hydraulic conductivity, leaf resistance     

On temperature-independent growth of phytoplankton

Growth rates of two freshwater diatoms and three chlorophyteswere compared under 3 h days at 10 µmol m^–2 s^–1.Specific growth rates ranged between µ=0.03 day^–1and µ=0.055 day^–1 for the different species andwere in every species independent of temperature between 8 and16°C.