Seasonal photosynthetic activity of autotrophic picoplankton in Lake Kinneret, Israel

Autotrophic picoplankton populations in Lake Kinneret are composedof picocyanobacteria and picoeukaryotes. Overall, the ratesof photosynthetic carbon fixed by autotrophic picoplankton duringthis study were low (0.01–1.5 mg Cm^–3 h^–1).The highest chlorophyll photosynthetic activity of the <3µm cell-size fraction was found in spring, when picoeukaryotespredominated and in addition small nanoplankton passed throughthe filters. The maximum cell-specific photosynthetic rate ofcarbon fixation by picocyanobacteria and picoeukaryotes was2.5 and 63 fg C cell^–1 h^–1, respectively. The highestspecific carbon fixation rate of autotrophic picoplankton was11 µg C µg^–1 Chl h^–1 The proportionalcontribution of autotrophic picoplankton to total photosynthesisusually increased with depth. Picocyanobacteria collected fromthe dark, anaerobic hypolimnion were viable and capable of activephotosynthesis when incubated at water depths within the euphoticzone. Maximum rates of photosynthesis (P_max) for picocyanobacteriaranged from 5.4 to 31.4 fg C cell^–1 h^–1 with thehighest values in hypolimnetic samples exposed to irradiance.Photosynthetic efficiency (     

Diurnal and seasonal variation in the contributions of autotrophic pico-, nano- and microplankton to the primary production of an upland lake

An investigation of the diurnal variation in productivity andcontribution to production of populations of autotrophic picoplankton(0.2–2.0 µm), nanoplankton (>2 <20 µm)and microplankton (>20 µm) was carried out at monthlyintervals, from May to October 1989, in Llyn Padarn a mesotrophicupland lake in North Wales. Maximum rates and contributionsto production of the lake by autotrophic picoplankton occurredduring mid-late summer, with the highest average daily contributionfrom picoplankton (64%) recorded in September at 4 m depth.Diurnal variation in contributions from picoplankton was pronounced,with greatest input, recorded at the end of the day, duringthe period of picoplankton dominance in mid-late summer. Maximumcontribution from picoplantkon (86% of total, 9.2 mg C m^–3h^–1) was recorded in September. Nanoplankton primary productionwas of greatest significance in June and July, although levelswere lower than for picoplankton in subsequent months. Contributionsvia nanoplankton increased with depth in the lake at this time,reaching a maximum of 78% of the total at the end of the dayat 9 m depth in early July. At this time, diurnal variationin contributions via nanoplankton was considerable, with maximumphotosynthesis generally at the end of the photoperiod at depthsof 4 and 9 m. Microplankton made the greatest impact on primaryproduction during the mixed water conditions of spring and autumn,and at these times did variation in production was less thanthose of both pico and nanoplankton during summer thermal stratification.Photosynthetic capacity was lower for picoplankton than fornanoplankton and microplankton; the highest values were 5, 33and 51 mg C (mg chl a)^–1) h^–1) for pico-, nano-and microplankton, respectively. The photosynthetic efficiencyof all three size categories of phytoplankton increased withdepth. Maximum values were similar for all phytoplankton groups,between 75 and 131 mg C (mg chl a)^–1) E^–1) m² butmean levels of photosynthetic efficiency for the 6 months werelower for picoplankton than for nano- or microplankton. Ratesof carbon fixation per cell for picoplankton spanned three ordersof magnitude, varied considerably diurnally and reached maximumvalues of 484 fg C(cell)^–1) h^–1) in the afternoonin near-surface waters in the early stages of exponential populationgrowth in July. During the population maximum of picoplanktonin August and September, maximum daily values of carbon fixationper cell, assimilation number and photosynthetic efficiencywere all recorded at the end of the day. The seasonal and diurnalpatterns of production of the three size categories of planktonicalgae in Llyn Padarn were distinct. During spring, microplankton(mainly diatoms) were the dominant primary producers. As thermalstratification developed, nanoplankton were the major contributorsto phytoplanktonic production, particularly in the deeper regionsof the euphotic zone. Picoplankton made the greatest contributionto production in August and September, exhibiting maximum inputtowards the end of the light cycle. Diatoms became the majorphotosynthetic plankton in the mixed water conditions prevalentin Uyn Padarn in October.     

Size structures of microplankton biomass and production in Jiaozhou Bay, China

Seasonal investigations of size-fractionated biomass and productionwere carried out from February 1992 to May 1993 in JiaozhouBay, China. Microplankton assemblages were separated into threefractions: pico- (0.7–2 µm), nano- (2–20 µm)and netplankton (20–200 µm). The biomass was measuredas chlorophyll a (Chi a), paniculate organic carbon (POC) andparticipate organic nitrogen (PON). The production was determinedby ¹⁴C and ¹⁵N tracer techniques. The seasonal patterns in biomass,though variable, were characterized by higher values in springand lower values in autumn and summer (for Chi a only). Theseasonal patterns in production, on the other hand, were moreclear with higher values occurring in summer and spring, andlower values occurring in autumn and winter. Averaged over thewhole study period, the respective proportions of total biomassaccounted for by net-, nano- and picoplankton were 26, 45 and29% for Chi a, 32, 33 and 35% for POC, and 26, 32 and 42% forPON. The contributions to total primary production by net-,nano- and picoplankton were 31, 35 and 34%, respectively. Therespective proportions of total NH₄⁺–N uptake accountedfor by net-, nano- and picoplankton were 28, 33 and 39% in thedaytime, and 10, 29 and 61% at night. The respective contributionsto total NO₃^–-N uptake by net-, nano- and picoplanktonwere 37, 40 and 23% in the daytime, and 13, 23 and 64% at night.Some comprehensive ratios, including C/N biomass ratio, Chla/C ratio, C uptake/Chl a ratio, C:N uptake ratio and the f-ratio,were also calculated size separately, and their biological andecological meanings are discussed.     

Diurnal variations in the contributions of autotrophic picoalgae and heterotrophic bacteria to planktonic production in an upland lake

An investigation of the diurnal variation in contributions toproduction of the autotrophic and heterotrophic components ofthe picoplankton community was carried out during August andSeptember in Llyn Padarn, a mesotrophic upland lake in NorthWales. The picoplankton was separated using 1 µm pore-sizedfilters into the smaller cell sized fraction (<1 µm),the majority of the bacteria and the larger cell sized picoalgae(<3>1 µm), together with some bacteria. The distributionof bacterial heterotrophic activity between these two fractionsof picoplankton was assessed by uptake of [¹⁴C]glucose and differentialfiltration. Thus, the absolute autotrophic production by picoalgaeand the heterotrophic contribution by bacteria to picoplanktoncommunity production via uptake of extracellular organic carbon(EOC) were determined. Rates of picoplankton community productionexhibited diurnal variation with maximum rates of 19.1 mg Cm^–3 h^–1 recorded at 18.00 h at 4 m depth in September.The bacterial contribution to picoplankton community productionincreased markedly between 15.00 and 18.00 h. Rates of absoluteautotrophic production varied less over 24 h than rates of accumulationin bacteria of ¹⁴C-labelled EOC released from the entire phytoplanktoncommunity. Bacteria contributed up to 86–98% of the neworganic carbon within the picoplankton community at the endof the day. The maximum rate of absolute autotrophic productionin the picoplankton was 1.6 mg C m^–3 h^–1 at 18.00h at 1 m in August, and the maximum rate of bacterial accumulationof new organic carbon was 18.5 mg C m^–3 h^–1 at 18.00h in September at 4 m depth. The diurnal pattern of picoplanktoncommunity production involved increasing rates during the daywith a maximum at 18.00 h. Autotrophic processes were dominantin the first 3–6 h of the light cycle and heterotrophicuptake of ¹⁴C-labelled EOC was the major component from 15.00h onwards. Bacterial uptake of newly released EOC by phytoplanktonwas rapid, comprised the majority of picoplankton production,particularly later in the day, and contributed a maximum of60% of the total pariculate primary production in plankton between15.00 and 18.00 h at 4 m in September with a mean contributionof between 6 and 26% over 24 h in these investigations. Theimportance of autotrophic processes in picoplankton communityproduction has been overestimated in previous investigations.Bacteria play a major role in transferring newly produced EOCrapidly from phytoplankton to the picoplankton community. Atthe end of the day, the majority of newly produced organic carbonis in bacterial cells and this production is significant inthe dynamics of carbon production within the entire planktoniccommunity.     

Autotrophic picoplankton in southern Lake Baikal: abundance, growth and grazing mortality during summer

Autotrophic picoplankton were highly abundant during the thermalstratification period in late July in the pelagic area (waterdepth 500–1300 m) of southern Lake Baikal; maximum numberswere 2 x 10⁶ cells ml^–1 in the euphotic zone ({small tilde}15m). Unicellular cyanobacteria generally dominated the picoplanktoncommunity, although unidentified picoplankton that fluorescedred under blue excitation were also abundant (maximum numbers4 x 10⁵ cells ml^–1) and contributed up to {small tilde}40%of the total autotrophic picoplankton on occasions. Carbon andnitrogen biomasses of autotrophic picoplankton estimated byconversion from biovolumes were 14–84 µg C l^–1and 3.6–21 µg N l^–1. These were comparableto or exceeded the biomass of heterotrophic bacteria. Autotropicpicoplankton and bacteria accounted for as much as 33% of paniculateorganic carbon and 81% of nitrogen in the euphotic zone. Measurementsof the photosynthetic uptake of [^l4C]bicarbonate and the growthof picoplankton in diluted or size-fractionated waters revealedthat 80% of total primary production was due to picoplankton,and that much of this production was consumed by grazers inthe <20 µ.m cell-size category. These results suggestthat picoplankton-protozoan trophic coupling is important inthe pelagic food web and biogeochemical cycling of Lake Baikalduring summer.     

Seasonal and interannual variability of size-fractionated phytoplankton biomass and community structure at station Kerfix, off the Kerguelen Islands, Antarctica

Time series of phytoplankton biomass and taxonomic compositionhave been obtained for the 3 years 1992, 1993 and 1994 in thenorthern part of the Southern Ocean (station Kerfix, 5040'S,6825;E) Autotrophic biomass was low throughout the year (<0.2mg m^–3 except during a short period in summer when a maximumof 1.2 mg chlorophyll (Chl) a m– was reached. During winter,the integrated biomass was low (<10 mg m^–2) and associatedwith deeply mixed water, whereas the high summer biomass (>20mg m^–2) was associated with increased water column stability.During summer blooms, the >10 µ;m size fraction contributed60% to total integrated biomass. Large autotrophic dinoflagellates,mainly Prorocentrum spp., were associated with the summer phytoplankton maxima and accounted for >80% of the total autotrophcarbon biomass. In November and December, the presence of thelarge heterotrophic dinoflagellates Protoperidinium spp. andGyro dinium spp. contributed a high proportion of total carbonbiomass. During winter, the <10 µm size fraction contributed80% of total Chi a biomass with domination of the picoplanktonsize fraction. The natural assemblage included mainly nakedflagellates such as species of the Prasinophyceae, Cryptophyceaeand Prymnesiophyceae. During spring, picocyanobacteria occurredin sub-surface water with a maximum abundance in September of106 cells 1^–1     

Community structure, biomass and productivity of size-fractionated summer phytoplankton populations in lower Narragansett Bay, Rhode Island

Seventeen size-fractionation experiments were carried out duringthe summer of 1979 to compare biomass and productivity in the< 10, <8 and <5 µm size fractions with that ofthe total phytoplankton community in surface waters of NarragansettBay. Flagellates and non-motile ultra-plankton passing 8 µmpolycarbonate filters dominated early summer phytoplankton populations,while diatoms and dinoflagellates retained by 10 µm nylonnetting dominated during the late summer. A significant numberof small diatoms and dinoflagellates were found in the 10–8µm size fraction. The > 10 µm size fraction accountedfor 50% of the chlorophyll a standing crop and 38% of surfaceproduction. The <8 µm fraction accounted for 39 and18% of the surface biomass and production. Production by the< 8 µm fraction exceeded half of the total communityproduction only during a mid-summer bloom of microflagellates.Mean assimilation numbers and calculated carbon doubling ratesin the <8 µm (2.8 g C g Chl a^–1 h^–1; 0.9day^–1)and<5 µm(1.7 g C g Chl a^–1h^–1; 0.5day^–1)size fractions were consistently lower than those of the totalpopulation (4.8 g C g Chl a^–1 h^–1; 1.3 day^–1)and the <10 µm size fraction (5.8 g C g Chl a^–1h^–1; 1.4 day ^–1). The results indicate that smalldiatoms and dinoflagellates in fractionated phytoplankton populationscan influence productivity out of proportion to their numbersor biomass. ¹Present address: Australian Institute of Marine Science, P.M.B.No. 3, Townsville M.S.O., Qld. 4810, Australia.     

Microzooplankton herbivory and bacterivory in Newfoundland coastal waters during spring, summer and winter

Grazing by microzooplankton on autotrophic and heterotrophicpicoplankton as well as >0.7 µm phytoplankton (as measuredby chlorophyll a) was quantified during July, August, October,January and April in the surface layer of Logy Bay, Newfoundland(47°38'14'N, 52°39'36'W). Rates of growth and grazingmortality of bacteria, Synechococcus and >0.7 µm phytoplanktonwere measured using the sea water dilution technique. Microzooplanktoningested 83–184, 96–366 and 64–118% of bacterial,Synechococcus and >0.7 µm phytoplankton daily potentialproduction, respectively and 34–111, 25–30 and 16–131%of bacterial, Synechococcus and >0.7 µm phytoplanktonstanding stocks, respectively. The trends in prey net growthrates followed the seasonal cycles of prey biomass, suggestingthat microzooplankton are important grazers in Newfoundlandcoastal waters. Ingestion was lowest during January and October(~2 µg C l^–1 day^–1) and highest in August(~20 µg C l^–1 day^–1). Aside from April when>0.7 µm phytoplankton represented the majority (~80%)of carbon ingested, bacterioplankton and <1 µm phytoplanktonrepresented most of the carbon ingested (~40–100%). Althoughmicrozooplankton have here-to-fore been unrecognized as an importantgrazer population in Newfoundland coastal waters, these resultssuggest that they play an important role in carbon flow withinthe pelagic food web, even at low temperatures in Logy Bay.     

Carbon dynamics in the 'grazing food chain' of a subtropical lake

Studies were conducted over a 13 month period at four pelagicsites in eutrophic Lake Okeechobee, Florida (USA), in orderto quantify carbon (C) uptake rates by size-fractionated phytoplankton,and subsequent transfers of C to zooplankton. This was accomplishedusing laboratory ¹⁴C tracer methods and natural plankton assemblages.The annual biomass of picoplankton (<2 µm), nanoplankton(2–20 µm) and microplankton (<20 µm averaged60, 389 and 100 µg C 1^–1 respectively, while correspondingrates of C uptake averaged 7, 51 and 13 µg C1^–1h^–1. The biomass of microzooplankton (40–200 µm)and macrozooplankton (<200 µm averaged 18 and 60 µgC 1^–1, respectively, while C uptake rates by these herbivoregroups averaged 2 and 3 µg C 1^–1 h^–1. Therewere no strong seasonal patterns in any of the plankton metrics.The ratio of zooplankton to phytoplankton C uptake averaged7% over the course of the study. This low value is typical ofthat observed in eutrophic temperate lakes with small zooplanktonand large inedible phytoplankton, and indicates ineffectiveC transfer in the grazing food chain. On a single occasion,there was a high density (<40 1^–1) of Daphnia lumholrzii,a large-bodied exotic cladoceran. At that time, zooplanktoncommunity C uptake was <20 µg C 1^–1 h^–1and the ratio of zooplankton to phytoplankton C uptake was near30%. If D.lumholrzii proliferates in Lake Okeechobee and theother Florida lakes where it has recently been observed, itmay substantially alter planktonic C dynamics.     

Short-term changes of protozoan control on autotrophic picoplankton in an oligo-mesotrophic lake

In May 1994, we investigated the short-term development of theplanktonic community in the epi- and metalimnion of an oligo-mesotrophiclake (Piburger See, Tyrol), focusing on trophic links betweenprotists and picoplankton, but also including phyto- and zooplankton.Uptake experiments with fluorescently labelled bacteria (FLB)and picocyanobacteria (FIC) were performed in order to comparethe importance of both prey types as carbon sources for bacterivorousprotists. Heterotrophic nanoflagellates (HNF) were responsiblefor {small tilde}90% of total protozoan picoplanktivory (FLB+ FLC); ciliates accounted for {small tilde}10%. A selectivityindex related to prey density showed that both HNF and ciliatesclearly preferred FLC over FLB. The mean cell size of autotrophic(prokaryotic) picoplankton (APP) was nearly three times larger(0.323 µm³) and much less variable than mean bacterialcell volume (0.122 µm³). Although APP biomass was on averageonly 8.6% of total picoplankton biomass, pico-cyanobacteriaaccounted for a mean 15.9% of total HNF carbon uptake. We calculatedthat total HNF grazing could match potential APP maximum growthrates at the beginning of the study period. A strong decreasein HNF individual clearance rate (CR) on APP was clearly relatedto a fall in the percentage of choanofiagellates (from 75 to{small tilde}10% of the HNF community). A simultaneous decreasein HNF biomass and CR was followed by a steep increase in APPabundance; APP abundance and HNF biomass were highly negativelycorrelated both in the epi- and the metalimnion (r_{1 EM} = –0.879,r_{1 META} = =0.907; P = 0.001). Total rotifer abundance increasedby a factor of 50 within 2 weeks and was also negatively correlatedwith HNF biomass (r_{1 EM} = –0.852, P < 0.001; r_{1 META}= –0.659, P < 0.05). HNF grazing was found to exerta strong short-term control on picocyanobacteria and this linkwas probably broken by an increase in metazooplankton, especiallydue to rotifer predation on HNF.     

Productivity of picoplankton compared with that of larger phytoplankton in the subarctic region

We determined the productivity (µg C µg^–1Chi a h^–1) of size-fractionated phytoplankton in the northernNorth Pacific and the Bering Sea in summer and winter. Picoplankton(<2 µm) were more productive than larger sized phytoplankton(2–10 and 10–200 µm) in the subtropical region,where the in situ temperature was >10°C; whereas picoplanktonin the subarctic region were similar in productivity or lessproductive than larger sized plankton, where the in situ temperaturewas <10°C. The result from the subtropical region inthis study agrees with previous results from tropical and subtropical waters, which indicate that phytoplankton productivitytends to decrease with increasing cell size. The result fromthe subarctic region, however, differs from previous results.We observed a positive linear regression for in situ temperatureand picoplankton productivity, but this trend was not seen inthe larger sized phytoplankton. The results show that the productivityof picoplankton is markedly influenced by in situ temperaturecompared with that of larger sized plankton. Low tem peratureappears to account largely for the observation that the productivityof picoplankton is not significantly higher than that of largersized phytoplankton in the subarctic region.     

Red tide assemblage formation in an estuarine upwelling ecosystem: Ria de Vigo

Red tides are conspicuous in the upwelling system of Galicia(NW Iberian Peninsula). At present, there are conflicting hypothesesabout the generation site of these phytoplankton assemblages.It is interesting to know whether the rias can be sites of redtide formation or if they act only as accumulation sites ofpopulations advected from shelf waters. A study in the Ra deVigo, carried out during late September 1990, showed the developmentof a red tide assemblage, composed of Alexandrium affinis, Ceraiiumfusus and Gymnodinium catenaium, during a 2 week upwelling-downwellingcycle. Growth occurred at the bottom of the thermocline-topof the nutricline. Above this assemblage, a diatom assemblage(large diatoms) was blooming. Prior to the formation of thered tide, a subsurface chlorophyll maximum made up of smalldiatoms (Nilzschia f. seriaia, Chaeloceros socialis), smallflagellates (<30 µm) and small gymnodinid forms (<30µm) was observed. In the nutrient-depleted upper layer,several autotrophic and large heterotrophic dinoflagellatesdominated. It is suggested that the ratio between the velocityof upward water movement and the depth of the stratified upperlayer (flushing rate, day^–1) is the critical parameterwhich triggers active phytoplankton growth. It can be concludedthat upward water velocities of {small tilde}2.5 m day^–1and a stratified upper layer of 10 m depth (flushing rate 0.25day^–1) are the main physical constraints for red tidedevelopment.     

Contribution of Picocyanobacteria to total primary production and community respiratory losses in a backwater system

The contribution of autotrophic picoplankton (APP) to phytoplanktonicprimary production, investigated during the phytoplankton growingseason (March–September) in a macrophyte-dominated backwatersystem near Vienna, showed that APP mainly consisted of rod-shapedand coccoid cyanobacteria. Two stations were examined, exhibitingsimilar seasonal patterns in the development of picocyanobacteria,although the two sites differed in picocyanobacterial cell numbersand biomass by a factor of 1.5. Cell numbers determined by epifluorescencemicroscopy varied between 0.29 x 10⁴ and 34.5 x 10⁴ cells ml^–1at Station 1, and between 0.23 x 10⁴ and 19.1 x 10⁴ cells ml^–1at Station 2. At both sites, the mean cell volume of picocyanobacteriawas 0.5 µm³. Carbon fixation in the planktonic communityof the Kühwörter Wasser was dominated primarily bylarger phytoplankton, although the picoplankton community sometimessupplied up to 74% (mean: 35%) of total primary production.Distinct differences in chlorophyll a concentrations and primaryproduction between the two sites refer to a greater competitionbetween phytoplankton and macrophytes at Station 2. Communityrespiration deviated greatly in time and in level at the twostations, showing a higher dynamic in community metabolism atStation 1. At this site, community respiration losses rangedbetween 12 and 100% of gross production. Hence, community metabolismcomprised net autotrophic, balanced, and net heterotrophic situationsover the investigation period, whereas at Station 2, only netautotrophic situations could be determined.     

On the distribution and importance of picocyanobacteria in a boreal inshore area (Kiel Bight, Western Baltic)

From April to October 1986 abundance and vertical distributionof picocyanobacteria were studied at four stations in Kiel Fjordand Kiel Bight. Both picocyanobacteria and autotrophic, eukaryoticpicoplankton cell numbers were estimated by epifluorescencemicroscopy whereas larger phytoplankton (>3 µm) wasenumerated by the Utermöhi settling technique. Picocyanobactenacell numbers peaked in July and August near the water surface(1.4–2.6 x 10⁸ cells l^–1). Although picocyanobacteriaabundance increased from the outer Kiel Bight to the more eutrophicinner stations of Kiel Fjord, their contribution to total phytoplanktonbiomass decreased. During summer up to 52% of phytoplanktoncarbon and up to 97% of autotrophic picoplankton carbon werecontributed by picocyanobacteria. Therefore picocyanobacteriaare an important component of the summer phytoplankton communityin boreal inshore waters, too.     

Nitrogen dynamics in lower Narragansett Bay, Rhode Island. I. Uptake by size-fractionated phytoplankton populations

The contribution of nanoplankton (< 10 µm fraction)to winter – spring (1977 – 78) and summer (1978,1979) phytoplankton nitrogen dynamics in lower NarragansettBay was estimated from ammonium, nitrate and urea uptake ratesmeasured by ¹⁵N tracer methods. During the winter – spring,an average of 80% of chlorophyll a and nitrogen uptake was associatedwith phytoplankton retained by a 10 µm screen. In contrast,means of 51 – 58% of the summer chlorophyll a standingcrops and 64 – 70% of nitrogen uptake were associatedwith cells passing a 10 µm screen. Specific uptake ratesof winter – spring nanoplankton populations were consistentlylower than those of the total population. Specific uptake ratesof fractionated and unfractionated summer populations were notsignificantly different. Ammonium uptake averaged between 50and 67% of the total nitrogen uptake for both the total populationand the < 10µm fraction. The total population and the10 µm fraction displayed similar preferences for individualnitrogen species. Though composed of smaller cells, flagellatedominated nanoplankton assemblages may not necessarily takeup nitrogen at faster rates than diatom dominated assemblagesof larger phytoplankters in natural populations. ¹Present address: Australian Institute of Marine Science, P.M.B.No. 3, Townsville M.S.O., Qld. 4810, Australia     

Predation and respiration by the small cyclopoid copepod Oithona similisr: How important is feeding on ciliates and heterotrophic flagellates?

Feeding on natural plankton populations and respiration of thesmall cyclopoid copepod Oithona similis were measured duringthe warm season in Buzzards Bay, Massachusetts, USA. AlthoughO.similis did not significantly ingest small autotrophic andheterotrophic flagellates (2–8 µn), this copepodactively fed on >10 µm particles, including autotrophic/heterotrophic(dino)flagel-lates and ciliates, with clearance rates of 0.03–0.38ml animal^–1 h^–1. The clearance rates increased withthe prey size. O.similis also fed on copepod nauplii (mainlycomposed of the N1 stage of Acartia tonsa with a clearance rateof 0.16 ml animal^–1 h^–1. Daily carbon ration fromthe combination of these food items averaged 148 ng C animal^–1day^–1 (41% of body C day^–1), with ciliates and heterotrophicdino-flagellates being the main food source ({small tilde}69%of total carbon ration). Respiration rates were 020–0.23µl O₂ animal^–1 day^–1. Assuming a respiratoryquotient of 0.8 and digestion efficiency of 0.7, the carbonrequirement for respiration was calculated to be 125–143ng C animal^–1 day^–1, close to the daily carbon rationestimated above. We conclude that predation on ciliates andheterotrophic dinoflagellates was important for O.similis tosustain its population in our study area during the warm season.     

Spatial distribution of transparent exopolymer particles in the Bransfield Strait, Antarctica

Transparent exopolymer particles (TEP) are recognized to playan important role in the flux of exported carbon to the deepocean. However, there is little information on how TEP standingstocks are affected by different hydrographic conditions andother relevant ecological factors in situ. This lack of knowledgeis particularly serious for the Southern Ocean. During Australsummer 1999, the Strait of Bransfield presented high mesoscalevariability. Two fronts were present, the Bransfield hydrographicfront and a slope front along the South Shetland Islands andseveral mesoscale anticyclonic eddies and/or frontal meanders.The spatial distributions of biological properties were largelyaffected by this complex hydrography. Chlorophyll a (Chl a)(0.05–4.81 µg L^–1), TEP (from undetectableto 346 µg GXeq L^–1) and heterotrophic bacteria (HB)(1.7–9.4 x 10⁵ cells mL^–1) were positively correlateddespite the wide hydrographic heterogeneity of the BransfieldStrait. Higher abundances of autotrophic biomass, and correspondlyhigher TEP and heterotrophic bacteria (HB), were found in themore stratified waters. TEP spatial distribution was mostlyrelated to the abundance of autotrophic biomass although localhigh TEP concentrations were not matched by similarly high valuesof Chl a in some areas where diatoms were relatively abundant.     

Composition and distribution of the pelagic and sympagic algal assemblages in the Laptev Sea during autumnal freeze-up

The phytoplankton and ice algal assemblages in the SiberianLaptev Sea during the autumnal freeze-up period of 1995 aredescribed. The spatial distribution of algal taxa (diatoms,dinoflagellates, chrysophytes, chlorophytes) in the newly formedice and waters at the surface and at 5 m depth differed considerablybetween regions. This was also true for algal biomass measuredby in situ fluorescence, chlorophyll (Chl) a and taxon-specificcarbon content. Highest in situ fluorescence and Chl a concentrations(ranging from 0.1 to 3.2 µg l^–1) occurred in surfacewaters with maxima in Buor Khaya Bay east of Lena Delta. Thealgal standing stock on the shelf consisted mainly of diatoms,dinoflagellates, chrysophytes and chlorophytes with a totalabundance (excluding unidentified flagellates <10 µm)in surface waters of 351–33 660 cells l^–1. Highestalgal abundance occurred close to the Lena Delta. Phytoplanktonbiomass (phytoplankton carbon; PPC) ranged from 0.1 to 5.3 µgC l^–1 in surface waters and from 0.3 to 2.1 µg Cl^–1 at 5 m depth, and followed the distribution patternof abundances. However, the distribution of Chl a differed considerablyfrom the distribution pattern shown by PPC. The algal assemblagein the sea ice, which could not be quantified due to high sedimentload, was dominated by diatom species, accompanied by dinoflagellates.Thus, already during the early stage of autumnal freeze-up,incorporation processes, selective enrichment and subsequentgrowth lead to differences between surface water and sea icealgal assemblages.     

Midwater macroplankton of British Columbia studied by submersible PISCES IV

Data are reported from 30 dives during winter and spring 1980–83at sites in the Strait of Georgia and inlets running off it,and in inlets on the west coast of Vancouver Island. Observationswere made from the surface to the bottom (maximum 733 m) butmost attention was given to the midwater plankton community.The vertical distribution and abundance of hydromedusae, siphonophores,ctenophores, euphausiids, pelagic worms and molluscs were recordedsystematically, along with data for one copepod species (Neocalanusplumchrus). The midwater environment was found to be stablein terms of species composition and depth ranges, which permittedthe data for several years and many locations to be pooled.Four categories of plankton are recognized: (a) epipelagic (concentratedin the top 50 m); (b) mesopelagic (50–175 m); (c) bathypelagic(below 175 m); and (d) meso-bathypelagic (forms living in bothmeso- and bathypelagic zones). Species in this last categorybehave like mesopelagic forms at the upper end of their ranges,migrating to the surface at night. Deeper-lying members of thesame species do not migrate. For six such species, the cut-offpoint between migratory and non-migratory components was foundto lie at a mean depth of 175 m. This depth is therefore takenas the demarcation point between the meso- and bathypelagiczones. Taking account of published data on light penetration,it is estimated that, for the whole region, daytime light intensityat 175 m, and hence the effective limit for phototaxis of thespecies in question, lies in the range 10^–8–10^–9µW cm^–2.     

Seasonal variations of bacterial abundance and biomass and their relation to phytoplankton in the hypertrophic tropical lagoon Cienaga Grande de Santa Marta, Colombia

The seasonal development of bacteria was studied in the hypertrophiccoastal lagoon Ciénaga Grande de Santa Marta (Caribbeancoast of Colombia). This large but only 1.5 m deep lagoon issubject to strong seasonal variations of salinity from almostfully marine (April/May) to brackish conditions in October/November.Chlorophyll ranged from 6 to 182 µg L^–1, and grossprimary production amounted to 1690 g C m^–2 per year.Total bacterial number (TBN) ranged from 6.5 to 90.5 x 10⁹ cellsL^–1 and bacterial biomass (BBM) from 77 to 1542 µgC L^–1, which are among the highest ever reported for naturalcoastal waters. Neither TBN nor BBM varied significantly withsalinity, phytoplankton or seston concentrations. Only the bacterialmean cell volume showed a significant relation to salinity,being highest (0.066 µm³) during the period of increasingand lowest (0.032 µm³) during decreasing salinity. Bacterialprotein accounted for 24% (19–26%) and phytoplankton proteinfor 57% (53–71%) of total seston protein. The ratio (annualmean) of bacterial carbon to phytoplankton carbon was 0.44 (range0.04–1.43). At low phytoplankton abundance [chlorophylla (Chl a) < 25 µg L^–1], bacterial carbon wasalmost equal to phytoplankton biomass (i.e. the mean ratio was1.04). In contrast, at Chl a > 100 µg L^–1, BBMwas low compared to phytoplankton biomass (the mean ratio was0.16). In general, BBM varied less than phytoplankton biomass.Most probably, the missing correlation between bacterial andphytoplankton variables was due to (i) organic material partlyderived from allochthonous sources serving as food resourcefor bacteria and (ii) a strong resuspension of bacteria fromthe sediment caused by frequent wind-induced mixing of the veryshallow lagoon.