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.     

Trophic links in the lowland River Meuse (Belgium): assessing the role of bacteria and protozoans in planktonic food webs

Trophic interactions within the plankton of the lowland RiverMeuse (Belgium) were measured in spring and summer 2001. Consumptionof bacteria by protozoa was measured by monitoring the disappearanceof ³H-thymidine-labelled bacteria. Metazooplankton bacterivorywas assessed using 0.5-µm fluorescent microparticles (FMPs),and predation of metazooplankton on ciliates was measured usingnatural ciliate assemblages labelled with FMPs as tracer food.Grazing of metazooplankton on flagellates was determined throughin situ incubations with manipulated metazooplankton densities.Protozooplankton bacterivory varied between 6.08 and 53.90 mgC m^–3 day^–1 (i.e. from 0.12 to 0.86 g C^–1bacteria g C^–1 protozoa day^–1). Metazooplankton,essentially rotifers, grazing on bacteria was negligible comparedwith grazing by protozoa (1000 times lower). Predation of rotiferson heterotrophic flagellates (HFs) was generally low (on average1.77 mg C m^–3 day^–1, i.e. 0.084 g C^–1 flagellatesg C^–1 rotifers day^–1), the higher contribution ofHF in the diet of rotifers being observed when Keratella cochleariswas the dominant metazooplankter. Predation of rotifers on ciliateswas low in spring samples (0.56 mg C m^–3 day^–1,i.e. 0.014 g C^–1 ciliates g C^–1 rotifers day^–1)in contrast to measurements performed in July (8.72 mg C m^–3day^–1, i.e. 0.242 g C^–1 ciliates g C^–1 rotifersday^–1). The proportion of protozoa in the diet of rotiferswas low compared with that of phytoplankton (<30% of totalcarbon ingestion) except when phytoplankton biomass decreasedbelow the incipient limiting level (ILL) of the main metazooplantonicspecies. In such conditions, protozoa (mainly ciliates) constituted50% of total rotifer diet. These results give evidence thatmicrobial organisms play a significant role within the planktonicfood web of a eutrophic lowland river, ciliates providing analternative food for metazooplankton when phytoplankton becomesscarce.     

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.     

Photosynthetic organic carbon production and respiratory organic carbon consumption in the trophogenic layer of Lake Biwa

Measurement of the photosynthetic production rate in Lake Biwawas camed out from May 1985 to September 1987. In the light-saturatedlayer, the seasonal variation in the photosynthesis rate perchlorophyll a was regulated by water temperature. The depth-integratedphotosynthetic production rate was 0.21-1.48 g C m^–2 day^–1and the maximum value was observed in midsummer when the watertemperature of the mixed surface layer was highesL The criticalnutrient for photosynthesis may be dissolved reactive phosphorus,which was generally <1 µg P 1^–1 throughout theobservation period. In the trophogenic layer, respiratory organiccarbon consumption, estimated from measurement of respiratoiyelectron transport system activity, was 0.35-1.07 (mean 0.66)g C m^–1 day^–1 and corresponded, on average, to 79%of the photosynthetic carbon production rate. This implies thatthe major part of photosynthetic fixed organic matter mightbe recycled in the trophogenic layer. The estimated settlingorganic carbon flux at 20 m depth, from calculation of theseparameters and changes in the particulate organic carbon concentration,was 0.01 (-0.09 to 0.13) g C m^–1 day^–1 The meansettling organic carbon flux measured by sediment trap at 20m was 0.19 (0.09-0.31) g C m^–1 day^–1 higher thanthe estimated value. It seemed that organic matter collectedby sediment trap may contain allochthonous matter and resuspendedepilimnetic sediment matter.     

Size-fractionated primary production studies in the vicinity of the Subtropical Front and an adjacent warm-core eddy south of Africa in austral winter

Results are presented of size-fractionated primary productionstudies conducted in the vicinity of the Subtropical Front (STF),an adjacent warm-core eddy, and in Sub-antarctic waters duringthe third South African Antarctic Marine Ecosystem Study (SAAMESIII) in austral winter (June/July) 1993. Throughout the investigation,total chlorophyll (Chl a) biomass and production were dominatedby small nano- and picophytoplankton. No distinct patterns intotal Chl a were evident. At stations (n = 7) occupied in thevicinity of the STF, total integrated biomass values rangedfrom 31 to 53 mg Chl a m^–2. In the vicinity of the eddy,integrated biomass at the eddy edge (n = 3) ranged from 24 to54 mg Chl a m^–2 and from 32 to 43 mg Chl a m^–2 inthe eddy (n = 2). At the station occupied in the Sub-antarcticwaters, total integrated biomass was 43 mg Chl a m^–2.Total daily integrated production was highest at stations occupiedin the vicinity of the STF and at the eddy edge. Here, totalintegrated production ranged from 150 to 423 mg C m^–2day^–1 and from 244 to 326mg C m^–2 day^–1, respectively.In the eddy centre, total integrated production varied between134 and 156 mg C m^–2 day^–1. At the station occupiedin the Sub-antarctic waters, the lowest integrated production(141 mg C m^–2 day^–1) during the entire survey wasrecorded. Availability of macronutrients did not appear to limittotal production. However, the low silicate concentrations duringthe survey may account for the predominance of small nano- andpicophytoplankton. Differences in production rates between theeddy edge and eddy core were related to water column stability.In contrast, at stations occupied in the vicinity of the STF,the control of phytoplankton production appears to be relatedto several processes, including water column stability and,possibly, iron availability.     

Seasonal nitrogen assimilation and carbon fixation in a fjordic sea loch

Carbon (C) fixation and nitrogen (N) assimilation rates havebeen estimated from ¹⁴C and ¹⁵N techniques for a 12 month periodin a Scottish sea loch. The maximum rate of nitrogen assimilated(29.92 mmol N m^–2 day^–1) was in April at the mostseaward station; similar high rates were experienced duringMay at the other stations. Carbon fixation rates were maximal(488–4047 mg C m^–2day^–1) at the time of highphytoplankton biomass (maximum 8.3 mg m^–3 chlorophylla) during May, whilst nitrate concentrations remained >0.7µ.mol l^–1. C:N assimilation ratios suggest nitrogenlimitation only during the peak of the spring bloom, althoughat times nitrogen (nitrate and ammonium) concentration fellto 0.2 µmol l^–1 in the following months. The verticalstability of the water column, influenced by tidal and riverineflushing, varied along the axis of the loch, resulting in markeddifferences between sampling stations. Although ammonium waspreferentially assimilated by phytoplankton, >50% of productionwas supported by nitrate uptake and only during the summer monthswas the assimilation of ammonium quantitatively important.     

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.     

The contribution of ammonia excreted by zooplankton to phytoplankton production in Narragansett Bay

Ammonia excreted by mixed zooplankton populations over an annual(1972–1973) cycle in Narragansett Bay varied from 0.04to 3.21 µg at NH₃-N dry wt^–1 day^–1, exclusiveof two exceptional rates measured one year apart: 11.74 and18.39 µg at NH³-N mg dry wt^–1 day^–1. Grossphytoplankton production integrated over the year (1972–1973)averaged 151 mg C m^–3 day^–1 for an 8 m water column;peaks of 332 and 905 mg C m^–3 day^–1 occurred duringthe winter-spring and summer blooms, respectively. Excretedammonia, integrated seasonally and annually, contributed only0.2% and 4.9% of the nitrogen required for observed gross productionduring the winter-spring and summer blooms, respectively, and4.4% annually. However, excreted ammonia may be an importantsource of the nitrogen required by Skeletonema costatum, thedominant diatom in Narragansett Bay, during the post-bloom periodwhen 186% of the nitrogen required for its net production wasmet by ammonia excretion. A combination of zooplankton ammoniaexcretion and benthic ammonia flux contributed 22% of the nitrogenrequired for the annual gross production (440 g C m^–2)while 51% of the nitrogen required for the net production ofSkeletonema was accounted for by regenerated nitrogen. ¹This research was supported by NSF grant GA 31319X awardedto Dr.T.J.Smayda.     

Microplankton and its function in a zone of shallow hydrothermal activity:the Craternaya Bay, Kurile Islands

Biomass and productivity of microplankton were measured in theCraternaya Bay (Kurile Islands), which is influenced by hydrothermalactivity and volcanic heating. The hydrothermal fields are situatedaround its shores and underwater within the 0–20 m depth.A dense ‘bloom’ of photoautotrophic microplanktonwas observed there, dominated by diatoms, phytoflagellates andthe symbiont-containing ciliate Mesodinium rubrum. The biomassof these ciliates attained 3–11 g m^-3 in the upper waterlayer. The total biomass of the phototrophic microplankton reached30–46 g m^-3. The primary production in the water columnwas, correspondingly, enormously high: 6–10 g C m^-2 day^-1.The depth of the euphotic zone was 7 m. Pelagic photosynthesiswas inhibited in the upper 0–1 m by the spreading of alayer of low-salinity hydrothermal water. The numerical densityof bacterioplankton in the upper zone of the water column variedfrom 1 x 10⁶ to 2.9 x 10⁶ cells ml^-1, and its wet biomass from250 to 750 mg m^-3. Its production varied at stations from 70to 390 mg m^-3 day^-1. Chemosynthesis contributed up to 30% ofthis production in the sites neighbouring the hydrothermal vents.Outside their direct impact however, its share was negligible.The biomass of heterotrophic planktonic ciliates varied from30 to 270 mg m^-3. The mechanisms of possible influence of shallowvolcanic activity on development and function of microplanktonin the Craternaya Bay is discussed.     

Microplankton and primary production in the Sea of Okhotsk in summer 1994

Phytoplankton composition, density, vertical distribution andprimary production were investigated in the Sea of Okhotsk andin the adjacent northern north Pacific in July–August1994, together with measurements of density and distributionof planktonic microheterotrophs: bacteria, nanoheterotrophsand ciliates. Different phases of phytoplankton seasonal successionwere encountered during the period of investigation in variousregions of this sea. Primary production measured at 144 stationswas found to be greatest (1.5–4 g C m^-2day^-1) in areasof spring-phase succession along the Sakhalin shelf and theKashevarov bank. Periodic relapses of the spring blooms of ‘heavy’diatoms during the whole growth season were recorded over thisbank. The summer phase of the phytoplankton minimum prevailedin the central and eastern parts of the sea, manifested by thedominance of nanoflagellates in terms of phytoplankton biomass.Primary production was 0.5–1 g C m^-2 day^-1. The earlyautumn phase of succession was typical of the Kurile straitarea and the adjacent north Pacific. Primary production therevaried from 0.7 to 2 g C m^-2 day^-1. The integrated phytoplanktonbiomass in the water column varied from 9–12 g m^-2 inzones supporting the summer minimum assemblage to 15–20g m^-2 in zones of early autumn recovery of phytoplankton growth,and up to 40–70 g m^-2 in areas of remnant or relapseddiatom blooms. The numerical density of bacterioplankton wasbetween 1 x 10⁶ and 3 x 10⁶ cells ml^-1 and its wet biomass wasbetween 100 and 370 mg m^-3. In deep waters it was 8–15mg m^-3. The integrated bacterioplankton biomass in the upperwater column varied from 6 to 29 g m^-2. The numerical densityof zooflagellates varied in the upper layer between 0.8 x 10⁶and 4 x 10⁶ l^-1 and their biomass was between 20 and 50 mg m^-3.In deep waters they were still present at a density of 0.05x 10⁶ to 0.2 x 10⁶ cells l^-1. The biomass of planktonic ciliatesvaried between stations from 20 to 100 mg m^-3. The joint biomassof planktonic protozoa in the water column was between 3 and12 g m^-3 at most of the stations.     

Microzooplankton grazing in a coastal embayment off Concepcion, Chile, (~36{degrees} S) during non-upwelling conditions

The impact of grazing by natural assemblages of microzooplanktonwas estimated in an upwelling area (Concepción, Chile)during the non-upwelling season in 2003 and 2004. Seawater dilutionexperiments using chlorophyll a (Chl a) as a tracer were usedto estimate daily rates of phytoplankton growth and microzooplanktongrazing. Initial Chl a concentrations ranged from 0.4 to 1.4mg Chl a m^–3 and phytoplankton prey biomass and abundancewere numerically dominated by components <20 µm. Phytoplanktongrowth and microzooplankton grazing rates were 0.19–0.25day^–1 and 0.26–0.52 day ^–1, respectively.These results suggest that microzooplankton exert a significantremoval of primary production (>100%) during the non-upwellingperiod.     

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.     

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.     

Use of the Plastochron Index to Evaluate Effects of Light, Temperature and Nitrogen on Growth of Soya Bean (Glycine max L. Merr.)

The plastochron index (PI) has been compared with leaf growthand biomass accumulation in young soya bean plants of severalcultivars that were grown in controlled environments with differentirradiance levels and durations, temperatures, and nitrogen(N) regimes. Increasing the photoperiod from 10 to 16 h day^–1 increasedthe plastochron rate (PR) and the proportion of axillary growth.Doubling the photosynthetic photon flux density (PPFD) to 1000µmol m^–2S^–1, increased PR and the proportionof roots to total plant weight, but decreased the proportionof stems plus petioles to total. In a series of experiments,the plants were grown in an 8 h photoperiod at constant temperaturesof 17, 20, 26 or 32 °C. As temperature increased, PR increased,but the duration of leaf expansion decreased. Leaves were largestat 20 and progressively smaller at 26, 32 and 17 °C. Biomasswas greatest for a given PI at 20 °C and decreased in theorder of 26, 32, and 17 °C. The proportion of axillary growthalso was greatest at 20 °C. When plants were grown in a15 h photoperiod at temperatures from 17.1 to 26.6 °C, leafsize continued to increase up to the highest temperature. At17 °C, the PR in the 15 h photoperiod (PPFD 390 µmol;m^–2S^–1) was about threefold greater than in 8 h(500 µmol m^–2 S^–1); biomass accumulation perday was about fivefold greater. Increasing N from 3 to 36 mMincreased PR about 10 per cent, altered biomass partitioningamong plant parts, and increased the biomass of the plants.The NO₂ form of N markedly stimulated axillary growth as comparedwith the NH₄⁺ form. Environment or cultivar had little influenceon the duration of leaf expansion in terms of PI. Cultivarsdid not differ consistently in biomass production and allocationin the different environments. Glycine max (L.) Merrill, soybean, soya bean, plastochron index, leaf development, growth analysis, partitioning, light, nitrogen, temperature     

Basin-scale latitudinal patterns of copepod grazing in the Atlantic Ocean

Size-fractionated copepod abundance and ingestion rates wereinvestigated along a 50°S–50°Nlatitudinal transect,during the Atlantic Meridional Transect (AMT) 4, 5 and 6 cruises(boreal spring–autumn 1997, boreal spring–summer1998). Copepod abundance was higher at high latitudes in spring,near northwest Africa, in the equatorial and Benguela upwellingsystems, and in the Subtropical Convergence, and lower in oligotrophicgyres. Gut contents were not related to phytoplankton biomassor production. Gut evacuation rate averaged 0.03 min^-1, andwas not related to latitude or body size. Conservative estimatesof copepod community total ingestion rates ranged between 3.4and 173 mg C m^-2 day^-1 for AMT4, 1.6–252 mg C m^-2 day^-1in AMT5 and 10–160 mg C m^-2 day^-1 in AMT6. Maximum valueswere always in the upwelling regions, the subtropical convergenceand high latitudes in the Northern Hemisphere during borealspring. Calculated ingestion rates translate into average dailyminimal consumption values of 2.07%, 1.89% and 2.6% of totalchlorophyll stock, or 8.02%, 14.5% and 12.9% of total primaryproduction ingested daily on AMT4, 5 and 6 respectively. Grazingimpact increases considerably if we consider ingestion of phytoplanktonlarger than 2 µm, especially under the influence of theEquatorial and North African upwellings, where copepod ingestionrepresents up to 30% of the biomass and >100% of productionby large cells.     

Productivity of Daphnia longispina in a highly humic boreal lake

The development of the Daphnia longispina (O. F. Müller)population in a highly humic boreal lake was followed throughoutone growing season, and the amount of secondary production wasestimated in relation to primary production and available foodresources. The growth rate method was applied in the secondaryproduction measurements. Daphnia longispina did not appear inthe water column until 16 May, after which the animals werepresent throughout the growing season. The population showedthree density peaks; the first appeared in early June, and thesecond and third in mid-July and at the beginning of September,respectively. Somatic production followed a seasonal pattern,with highest production rates in midsummer. The maximum valueof 127 mg C m^–2day^–1 was recorded at the beginningof July. The total annual net production of D. longispina was7.9 g C m^–2. During most of the growing season, the primaryproductivity in the lake was well below 100 mg C m^–2 day^–1and the total annual productivity of photosynthetic algae was5.0 g C m^–2. We conclude that in this lake the zooplanktonpopulation did not rely on phytoplankton primary productionas a sole carbon source, but that most of the carbon must haveoriginated from bacterial production either directly or througha microbial loop.     

Size-fractionated Primary Production in the South Atlantic and Atlantic Sectors of the Southern Ocean

Results are presented from size fractionated chlorophyll a (Chla) and primary production studies along a transect between Antarcticaand southern Africa during the second South African AntarcticMarine Ecosystem Study (SAAMES II), conducted in late australsummer (January to February) 1993. Total integrated Chl a alongthe transect was highest in the vicinity of the Marginal IceZone (MIZ) and Antarctic Polar Front (APF). At these stations,integrated Chl a biomass was always >25 mg Chl a m^–2and was dominated by microphytoplankton. Although nominal increasesinChl a biomass were also associated with the Subantarctic Front(SAF) and Subtropical Convergence (STC), total Chl a biomassin these regions was dominated by nanophytoplankton. Withinthe inter-frontal regions, total integrated Chl a biomass waslower, generally <25 mg Chl a m^–2, and was always dominatedby nanophytoplankton. An exception was found in the AgulhasReturn Current (ARC) where picophytoplankton dominated. Totaldaily integrated production along the transect ranged between60 and 436 mg C m^–2 day^–1. Elevated production rateswere recorded at stations occupied in the vicinity of the MIZand at all the major oceanic frontal systems. The contributionsof the various size fractions to total daily production displayedthe same spatial pattern as integrated biomass, with microphytoplanktonbeing the most important contributor in areas characterizedby elevated phytoplankton biomass. Outside these regions, nanophytoplanktondominated the total phytoplankton production. Again, an exceptionwas found in the ARC north of the STC where picophytoplanktondominated total production. There, the lowest production alongthe entire transect was recorded, with total daily integratedproduction always <90 mg C m^–2 day^–1. The increasedproduction rates recorded in the MIZ appeared to result fromincreased water column stability as indicated by a shallow mixed-layerdepth. Within the inter-frontal regions, the existence of adeep mixed layer appeared to limit phytoplankton production.Low silicate concentrations in the waters north of the APF mayalso have limited the growth of large microphytoplankton.     

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.     

Noctiluca scintillans MACARTNEY in the Northern Adriatic Sea: long-term dynamics, relationships with temperature and eutrophication, and role in the food web

The first ‘bloom’ of Noctiluca scintillans in theNorthern Adriatic Sea was recorded in 1977. The organism causedseveral red tides in the whole basin during the late 1970s,a period characterized by increasing nutrient loads. Duringthe 1980s and early 1990s, there was no ‘red tide’,but the species was an almost constant summer presence, associatedwith high temperatures. Noctiluca scintillans was almost completelyabsent from 1994 until May 1997, concurrent with a general planktondecrease. From summer 1997, N. scintillans was recorded againin the whole basin, although there was no other signal of increasingeutrophication. In contrast to all previous observations, duringwinter 2002–2003, N. scintillans was continuously sampledin the Gulf of Trieste. We estimated experimentally growth andgrazing rates of the dinoflagellate at 9–10°C in cultureand consuming the natural assemblage. Noctiluca scintillanswas able to reproduce actively at low temperatures, showingsimilar growth rates in both experiments (k = 0.2 day^–1).The values found were close to those reported in the literaturefor higher temperatures. The natural diet was mainly composedof phytoplankton (ingestion = 0.008 µg C Noctiluca ^–1day^–1), microzooplankton (ingestion = 0.008 µg CNoctiluca ^–1 day^–1) and bacteria (ingestion = 0.005µg C Noctiluca ^–1 day^–1) with an average carboncontent of 0.138 ± 0.020 µg C Noctiluca cell^–1.     

Copepod abundance in the western Irish Sea: relationship to physical regime, phytoplankton production and standing stock

The distinct patterns of stratification in the North Channeland stratified region of the western Irish Sea influence theseasonal abundance of phytoplankton. The 3–4 month productionseason in the stratified region was characterized by productionand biomass peaks in the spring (up to 2378 mg C m² day^–1and 178.4 mg chlorophyll m^–2) and autumn (up to 1280 mgC m^–2 day^–1 and 101.9 mg chlorophyll m^–2).Phytoplankton in the North Channel exhibited a short, late productionseason with a single summer (June/July) peak in production (4483mg Cm^–2 day^–1) and biomass (–160.6 mg chlorophyllm^–2). These differences have little influence on copepoddynamics. Both regions supported recurrent annual cycles ofcopepod abundance with similar seasonal maxima (182.8–241.810³ind. m^–2) and dominant species (Pseudocalanus elongatusand Acartia clausi). Specific rates of population increase inthe spring were 0.071 and 0.048 day¹ for the North Channel andstratified region, respectively. Increased copepod abundancein the stratified region coincided with the spring bloom, andwas significantly correlated with chlorophyll standing stock.Increased copepod abundance preceded the summer production peakin the North Channel. This increase was not correlated withchlorophyll standing crop, suggesting that a food resource otherthan phytoplankton may be responsible for the onset of copepodproduction prior to the spring bloom. Hetero-trophic microplanktonas an alternative food source, and advection of copepods fromthe stratified region, are proposed as possible explanationsfor copepod abundance increasing in advance of the summer peakin primary production.