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.     

The size distribution of phytoplankton and participate organic matter in the Equatorial Atlantic Ocean: importance of ultraseston and consequences

The size fractionation of paniculate matter (<200, <35,<3 and <1 µm) has been measured in the EquatorialAtlantic Ocean at different stations. Chlorophyll a, phaeophytin,particulate carbon, nitrogen and phosphorus have been analysed.Primary production by ¹⁴CO₂ uptake was also measured with prescreeningtechnique. It appears from this study, that the pariculate matter has avery small size: 40–60% of the chlorophyll passed through1 µm Nucleopore filter, and 75–90% of the paniculatecarbon and nitrogen passed through 3 µm Nucleopore filterin offshore waters. From the atomic ratio C/N, C/P and C/chla, and primary productionvalues, the <3 µm fraction would be mainly constitutedby inactive photosynthetic organisms or partides of detritus.The 3–35 µm fraction, in contrast, would be principallyactive phytoplankton.     

Biomass, feeding and production of Noctiluca scintillans in the Seto Inland Sea, Japan

The abundance and biomass of the large heterotrophic dinoflagellateNoctiluca scintillans, together with the changes in its potentialprey items, were monitored in the Seto Inland Sea, Japan, duringsummer 1997 (17 July-11 August). Growth and grazing rates ofNscintillans fed natural plankton populations were also measuredeight and seven times, respectively, during the survey period.The abundance and biomass of N scintillans averaged over thewater column (19 m) were in the range 1–345 cells 1^–1(temporalaverage = 93 cell1^–1) and 0.1–49.6 µg C l^–1(temporalaverage = 13.8 µg C l^–1; three times higher thanthat of calanoid copepods during the same period). Noctilucascintillans populations followed the changes in phytoplankton:N.scintillans biomass was increasing during the period of diatomblooms and was at a plateau or decreasing during periods oflow chlorophyll a. The growth rates of N.scintillans (µ)were also consistent with the wax and wane of the N.scintillanspopulation: N.scintillans showed highest growth rates duringdiatom blooms. A simple relationship between µ and chlorophylla concentration was established, and the production of N.scintillanswas estimated using this relationship and the measured biomass.The estimated production averaged over the water column wasin the range >0.1–5.2 µg C l^–1 day^–1(temporalaverage = 1.4 µg C l^–1 day^–1; 64% of the productionof calanoid copepods during the same period). Diatom clearancerates by N.scintillans were in the range 0.10–0.35 mlcell^–1 day^–1, and the phytoplankton population clearanceby N.scintillans was >12% day^–1. Thus, although thefeeding pressure of N.scintillans on phytoplankton standingstock was low, N.scintillans was an important member of themesozooplank-ton in terms of biomass and production in the SetoInland Sea during summer.     

Response of phytoplankton and bacteria to nutrients and zooplankton: a mesocosm experiment

Although both nutrient inputs and zooplankton grazing are importantto phytoplankton and bacteria in lakes, controversy surroundsthe relative importance of grazing pressure for these two groupsof organisms. For phytoplankton, the controversy revolves aroundwhether zooplankton grazers, especially large cladocerans likeDaphnia, can effectively reduce phytoplankton populations regardlessof nutrient conditions. For bacteria, little is known aboutthe balance between possible direct and indirect effects ofboth nutrients and zooplankton grazing. However, there is evidencethat bacteria may affect phytoplankton responses to nutrientsor zooplankton grazing through direct or apparent competition.We performed a mesocosm experiment to evaluate the relativeimportance of the effects of nutrients and zooplankton grazingfor phytoplankton and bacteria, and to determine whether bacteriamediate phytoplankton responses to these factors. The factorialdesign crossed two zooplankton treatments (unsieved and sieved)with four nutrient treatments (0, 0.5, 1.0 and 2.0 µgphosphorus (P) l^–1 day^–1 together with nitrogen(N) at a N:P ratio of 20:1 by weight). Weekly sieving with 300µm mesh reduced the average size of crustacean zooplanktonin the mesocosms, decreased the numbers and biomass of Daphnia,and increased the biomass of adult copepods. Nutrient enrichmentcaused significant increases in phytoplankton chlorophyll a(4–5x), bacterial abundance and production (1.3x and 1.6x,respectively), Daphnia (3x) and total zooplankton biomass (2x).Although both total phytoplankton chlorophyll a and chlorophylla in the <35 µm size fraction were significantly lowerin unsieved mesocosms than in sieved mesocosms, sieving hadno significant effect on bacterial abundance or production.There was no statistical interaction between nutrient and zooplanktontreatments for total phytoplankton biomass or bacterial abundance,although there were marginally significant interactions forphytoplankton biomass <35 µm and bacterial production.Our results do not support the hypothesis that large cladoceransbecome less effective grazers with enrichment; rather, the differencebetween phytoplankton biomass in sieved versus unsieved zooplanktontreatments increased across the gradient of nutrient additions.Furthermore, there was no evidence that bacteria buffered phytoplanktonresponses to enrichment by either sequestering P or affectingthe growth of zooplankton.     

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.     

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.     

Development of Eodiaptomus japonicus Burckhardt (Copepoda, Calanoida) reared on different sized fractions of natural plankton

The nutritional value of different sized fractions of naturalplankton was investigated for the growth of Eodiaptomus japonicusBurckhardt by comparing the development of its naupliar andcopepodid stages fed on differentially fractionated planktonicassemblages of a eutrophic pond, at 20°C. Water filteredthrough a 0.8 µm Nuclepore filter, containing mainly smallcoccoid bacteria (0.45–0.6 µm in cell diameter),at a concentration of 82.7 µg C 1^–1 could not supportthe development of E.japonicus. The 3 µm filtered water,containing bacteria and picoalgae. at a total concentrationof 259 µg C 1^–1, supported development but not eggproduction. The 20 µm filtered water, containing bacteria,picoalgae and large algae, at a total concentration of 2600µg C 1^–1, supported rapid development of the juvenilesand continuous egg production by the adults. The separated 3–20µm fraction, containing only large algae, could not supportthe development at concentrations of 131 and 196 µg C1^–1. However, the same rapid development of the juvenilesand continuous egg production by adults occurred at all of thetested concentrations between 261 and 3920 µg C1^–1of the large algae. The results suggest that E.japonicus favoursalgae larger than 3 µm during its complete lifespan, andthat the threshold food concentration for its development variesbetween 200 and 250 µg C 1^–1.     

Why are there no picoplanktonic O2 evolvers with volumes less than 10-19 m3?

Non-scalable components occupy an increasing fraction of thebiomass of cells as their size decreases, thus decreasing thefraction of the biomass available for other scalable, essentialactivities. The non-scalable components include the genome,and membranes such as the plasrnalemma and the outer membraneof cyanobacteria and the plastid envelope membranes of chlorophytes.The predicted influences of the increasing fraction of non-scalablecomponents in small cells (0.5 µm radius spherical cellsrelative to 5 µm radius cells) are threefold. One predictionis a decreased maximum specific growth rate (biomass increaseper unit biomass per unit time) due to a decreased fractionof biomass occupied by scalable catalysts. This in turn givesa lower catalytic activity per unit biomass leading to a lowermaterial or energy conversion rate per unit biomass. A secondprediction is a reduced fraction of the biomass occupied bylight-harvesting material, thus partly or entirely removingthe photon-harvesting advantage of smaller cells and diminishingspecific growth rate at low incident photon flux densities.A third prediction is that the different C:N:P ratio in non-scalablecomponents compared to ‘average’ biomass means avariation in C:N:P ratio at low cell sizes, with a lower C:Nratio in smaller cells and a higher C:P ratio in small cyanobacterialcells, but a lower C:P ratio in smaller chlorophyte cells. Thedifference in C:P ratio predictions is a function of the higherDNA content of chlorophyte than cyanobacterial cells. Comparisonsof these predictions with the observed effects on cell propertiesand behaviour of variations in cell size in the range 0.3–2µm radius for cyanobacteria and 0.5–9 µm radiusfor chlorophytes yields the following results. The general trendfor an increase in maximum specific growth rate with decreasingcell size (a finding with little theoretical explanation) appearsto be reversed as cell size decreases below     

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     

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.     

Body size and mass flow in freshwater plankton: models and tests

Observations of radiotracer (³²P) flow in size-fractionatedlake plankton were compared with the predictions of size-dependentmodels of material flow. The models assume that the metabolicactivity and turnover of the size fractions can be describedas power functions of size (Y=aM^b) One model, called size-structured,is an application of the Platt and Denman formalism: it assumesthat materials are incorporated preferentially by the smallestorganisms and flow continuously toward the larger organisms.In this model, the trophodynamic flow from a size fraction isconstrained to the next larger fraction. The tracer data indicatedthat metabolic activity could indeed be described as a continuousfunction of size, at least within the microplankton (< 75µm), but it did not support the hypothesis of a size-hierarchicaltrophodynamic flow. Another model limited the size range ofpredators to the larger (> 10 µm), size fractions whilerelaxing the size dependence constraint on the trophodynamicflow. This ‘unstructured’ model agreed better withthe ³²P dynamics and generated estimates of seston P uptakeand of the rates of biomass turnover that compared favorablywith published estimates for oligotrophic lakes. Some problemswith the fit to the data remain but might be dealt with by distinguishinga priori among functional types of planktonic organisms throughfluorescence (flow cytometry) or metabolic properties (inhibitors).     

Annual pattern of micro- and mesozooplankton abundance and biomass in a subtropical estuary

The pattern of biomass and abundance of microzooplankton andmesozooplankton were studied over an annual cycle in the NuecesEstuary, Texas. Zooplankton samples and associated hydrographicdata were collected at four locations at biweekly intervalsfrom September 1987 through October 1988. This is a broad, shallowbay system with an average depth of 2.4 m. The concentrationof chlorophyll a in the surface waters averaged 7.4 µgl^–1with 85% passing through a 20 µ mesh. Microzooplankton(20–200 µ in length) were extremely abundant throughoutthis study. Abundances of ciliates (including both aloricateciliates and tintinnids) ranged from 5000 to 400 000 l^–,with a mean of 38 000 l^–1 of seawater over the entirecourse of the study. Mesozooplankton (200–2000 µmin length) abundance averaged 6100 m^–3 for samples collectedduring the day and 10 100 m^–3 for samples collected atnight. Mesozooplankton were dominated by Acartia tonsa whichmade up {small tilde}50% of the total. Biomass estimates formicrozooplankton (based on volume estimates) were often higherthan measured biomass of mesozooplankton. Given the shortergeneration times and higher metabolic rate of microzooplanktoncompared to mesozooplankton, microzooplankton should have agreater effect on the trophic dynamics of the Nueces Estuarythan mesozooplankton.     

Photoadaptation in Antarctic phytopfankton: variations in growth rate, chemical composition and P versus I curves

The response of phytoplankton to variations in the light regimewas studied during the VULCAN and ACDA cruises in the Antarctic.Unenriched batch cultures of 12–19 days' duration reachedchl concentrations of 10–50 µg^–1 and exhibitedexponential growth rates, with the maximal rate being 0.41 doubl,day^–1. Ice edge algae exhibited maximum growth rates atphoton flux densities (PFD) of 30–100 µE m^–2S^–1and the growth rate was reduced by about 30% at 500–1000µE m^–2S^–1 The chl/C ratio ranged between 0.004and 0.018, with the lowest ratios at PFDs above 500 µEm^–2S^–1 chl/C ratios were also below maximum at PFDsbelow 40–50 µE m^–2S^–1 The C:N:P ratioswere close to the Redfield ratios; the Si/C ratio averaged 0.16(atoms), and the ATP/C ratio averaged from 0.0024 to 0.0050in different culture senes. When thawed after having been frozenfor 10 days, shade-adapted cultures were in a much better conditionthan sun-adapted ones. P versus I data showed that the maximumassimilation number varied from 0.75 to 4.4 µg C (µgchl)^–1h^–1. It varied inversely with the chl/C ratio;therefore the maximum carbon turnover rate varied little betweensamples (0.024/0.035 h^–1). Low biomass communities exhibitedrelatively high values for (the initial slope of P versus Icurves), low values for 1_sat (160–330 µE m^–2S^–1),and they were susceptible to photoinhibition. In contrast, communitiesdominated by Odontella weissflogii exhibited low values for, a high value for I_sat (560 µE m^–2S^–1 andthey tolerated high PFDs. The photo-adaptational status of thephytoplankton in natural water samples is discussed relativeto the profile of water column stability and mixing processes.     

Population dynamics of bacterioplankton in an oligotrophic lake

The population ecology of bacterioplankton was studied overa 3 year period in Mirror Lake, an oligotrophic lake in thenortheastern USA. Bacterial population density, biomass, andrates of biomass production in the epilimnion and hypolimnionwere examined for their relationship with several environmentalparameters. Bacterioplankton density fluctuated between 0.5and 7 x l0 bacteria ml^–1, with highest values in the anoxichypolimnion. At all depths there was a trend towards a higherdensity of bacteria from spring to midsummer, followed by adecline in late summer to early autumn. Cocci tended to dominatebacterial cell shapes from winter to midsummer, after whichrod-shaped cells became most abundant. Rod-shaped cells contributedthe most to bacterioplankton biomass at all depths and timesof year. The mean annual biovolume of all bacterioplankton was0.12 µ cell^–1. The mean annual areal bacterioplanktonbiomass was 11–12 mmol C m^–2. The percentage ofbacterial to phytoplankton biomass per volume in summertimewas 27% in the epilimnion and 11% in the hypolimnion. Averageannual and summertime bacterial production estimated using the[3H]thymidine method was similar to previous estimates of bacterialproduction measured in Mirror Lake using other methods. Theaverage ratio of bacterial to net phytoplankton production pervolume was 0.34 in the epilimnion, and between 0.65 and 1 1.depending on depth, in the hypolimnion during summer. Of severalvariables considered in regression analyses, only temperatureexplained >50% of the variance in bacterial production inboth the hypolimnion and epilimnion. Above 14°C, however,bacterial production and growth rate in the epilimnion werenot clearly related to temperature. During the period of midsummerhypolimnetic anoxia, despite colder temperatures in the hypolimnion,bacterial production was up to 10 times greater than in theepilimnion.     

The seasonal abundance and production of Oithona nana (Copepoda:Cyclopoida) in Southampton Water

Recent studies indicate that Oithona spp. contribute significantlyto total copepod biomass. Little is known, however, about theirecological significance, particularly in the case of the estuarineOithona nana. A study comprising three sites within SouthamptonWater was conducted to evaluate the late-stage copepodite/adult(stages IV–VI) O. nana community, using 120-µm meshnets. Although present throughout the estuary, there was a strikingspatial gradient with O. nana most common in the upper estuary.A clear seasonal pattern was observed with O. nana as the mostabundant copepod species from late summer until early winter.It comprised 61% of all copepods recorded, with a biomass of757.22 mg C m^–3. Production estimates of O. nana werederived from the ‘instantaneous-growth’ approach,using appropriate growth equations. The estimated productionof O. nana ranged from 1.50 mg C m^–3 year^–1 withinthe lower estuary to 146.77 mg C m^–3 year^–1 in theupper estuary. In the upper estuary, this compares with productionrates of 187.47 mg C m^–3 year^–1 for all Acartiacongeners (excluding nauplii), the most common calanoid genus.Throughout the estuary, O. nana annual production represented18% of total copepod production clearly indicating that, atleast in the upper estuary, O. nana production may be directlycomparable with calanoid production.     

Phytoplankton and zooplankton seasonal dynamics in a subtropical estuary: importance of cyanobacteria

A seasonal study of phytoplankton and zooplankton was conductedfrom 1999 to 2001 in Pensacola Bay, Florida, USA, to furtherthe understanding of pelagic food webs in sub-tropical estuaries.Monthly measurements included size-fractionated chlorophyll(whole water, <5 µm, <20 µm), net- and picophytoplanktoncomposition analyzed using microscopy, flow cytometry, and HPLCpigment analysis. Additionally, zooplankton abundance and dryweight were determined from net tows. The results show a phytoplanktoncommunity dominated by the small size fraction (<5 µm),especially during the warm periods. The <5 µm chlorophyllfraction was strongly correlated with cyanobacterial abundanceand zeaxanthin. Cyanobacteria (cf. Synechococcus) abundancepeaked during summer in the upper estuary, typically exceeding3 x 10⁹ L^-1, and was strongly correlated with temperature. Cyanobacteriaabundance at the freshwater end of the Bay (in the EscambiaRiver) was very low, suggesting that cyanobacteria were notdelivered via freshwater. Two pigmentation types of cyanobacteriawere observed. Phycoerythrin-containing cells (PE-rich) weremore abundant at the marine end, while phycocyanin-containingcells (PC-rich) were more abundant in the upper estuary. Thelarger algae (>5–10 µm) were predominantly composedof diatoms, followed by chlorophytes, cryptophytes and dinoflagellates.The three most abundant genera of diatoms were Thalassiosira,Pennales and Cyclotella. Zooplankton biomass averaged 12.2 µgC L^-1, with peak biomass occurring during May (     

Phytoplankton and nutrients in the waters north-west of Spitsbergen in the autumn of 1979

Phytoplankton biomass, primary production rates and inorganicnutrients were measured in the uppermost layer of the ice-edgeregion and in open water and compared with environmental factorsduring a three-week cruise in September – October 1979.Biomass and production values were low (maximum 2.2 µgchl a l^–1, 2.5 mg C m^–3 h^–1). A post-bloomcommunity of diatoms, consisting mainly of representatives ofChaetoceros, Leptocylindrus, Nitzschia and Thalassiosira, waspredominant. Concentrations of phosphate were quite low (maximum0.55 µM I^–1). Nitrate and silicate ranged from nomeasurable quantities to 5.7 µM l^–1 and 3.8 µMl^–1, respectively. The possibility of light and nutrientlimitation on phytoplankton growth is discussed.     

Carbon and nitrogen content of Noctiluca scintillans in the Seto Inland Sea, Japan

The carbon and nitrogen content of Noctiluca scintillans cellsfrom the Seto Inland Sea, Japan was investigated in order toestimate its biomass in natural samples. The carbon contentof N.scintillans ranged from 123 to 627 ng C cell^–1 witha mean value of 353 ng C cell^–1, or 1.12 to 2.67 fg Cµm^–3 with a mean value of 1.98 fg C µm^–3.The nitrogen content ranged from 36.0 to 232 ng N cell^–1with a mean value of 131 ng N cell^–1, or 0.499 to 0.910fg N µm^–3 with a mean value of 0.694 fg N µm^–3.Total cell carbon and nitrogen increased but the carbon andnitrogen per cell volume decreased with increasing cell volume.The C/N ratio of the cells ranged from 2.3 to 4.4, which wasrelatively low compared with the Redfield ratio. The carbonand nitrogen content was extremely low (91.2 ng C cell^–1,41.8 ng N cell^–1) for starved cells, whereas it was extremelyhigh (528 ng C cell^–1, 205 ng N cell^–1) for cellswhich had ingested the large diatom, Coscinodiscus wailesii.Our results suggest that the carbon and nitrogen content ofN.scintillans varies depending on its physiological conditionand the type of food that it has recently consumed.     

Abundance and productivity of heterotrophic nanoplankton in Georgia coastal waters

The population abundances and rates of biomass production ofheterotrophic nanoplankton (HNAN) in Georgia coastal waterswere evaluated by epifluorescence microscopy. HNAN populations(mostly non-pigmented microflagellates <10 µm in diameter)ranged from 0.3 x 10³ cells ml^–1 in shelf waters 15 kmoffshore to 6.3 x 10³ cells ml^–1 in waters 0.25 km fromthe coast. There was a strong correlation (r = 0.83) betweenHNAN and free bacterioplankton population abundances, but noapparent relation (r = 0.38) between HNAN and phototrophic nanopLankton(PNAN) abundances. HNAN biomass production in estuarine andnearshore shelf waters, as estimated from increases in HNANpopulations during laboratory incubations of natural water samples,ranged from 0.10 to 0.79 mg C m^–3 h^–3, with populationgeneration times of 9.7 to 26.5 h. There was a significant linearrelation (r = 0.95) between HNAN biomass and HNAN productivity.We calculated that HNAN may graze at least 30% to 50% of dailybacterioplankton production in Georgia coastal waters.     

A comparison of performance of WP2 and MOCNESS

Zooplankton biomass in the Barents Sea was monitored during1988–97 using WP2 and MOCNESS plankton nets. These twosampling gears differ in their size and mode of operation. Theplankton samples were size fractionated into three categoriesand the dry weight per square metre was calculated. The smallestand the medium size fractions (< 2000 µm) representedmainly copepods, and the larger size fraction (> 2000 µm)consisted mainly of macrozooplankton such as krill and amphipods.WP2 biomass values were higher for the smallest size fraction,whereas the MOCNESS tended to give higher values for the largestsize fraction However, the total amount of zooplankton biomass(g m^–1) obtained by these two methods was not significantlydifferent.