Nanoflagellate predation on auto- and heterotrophic picoplankton in the oligotrophic Mediterranean Sea

Dynamics of autotrophic and heterotrophic prokaryotes and theirconsumption by nanoflagellates were studied in the euphoticzone at nine stations located from the Levantine Basin (34°E)to the Balearic sea (5°E) in June 1999. Bacterial biomassconstituted the largest proportion of living biomass at allstations. Integrated bacterial production at the furthest eaststation, was sixfold lower than integrated bacterial productionat the furthest west (13 and 75 mg C m^-2 d^-1 respectively).Estimated heterotrophic nanoflagellate bacterivory accountedfor 45–87% of bacterial production. Small protists (<3µm) dominated the bacterivore assemblage and accountedfor more than 90% of the heterotrophic bacterial consumption.Our results indicated that there was no negative selection againstSynechococcus and that both picoplankton groups were grazedaccording to their standing stocks. An estimated consumptionof Synechococcus derived from food vacuole content analysisof nanoflagellates revealed that they consumed from 0.5 to 45%(mean 13%) of Synechococcus stock per day. These data are amongthe first documenting the relative grazing impact of heterotrophicnanoflagellates on bacteria and Synechococcus in situ. Assumingthat there was no selection for or against Prochlorococcus,heterotrophic nanoflagellates could ingest from 1.4 to 21% (mean6%) of Prochlorococcus stock per day. The amount of organiccarbon obtained by heterotrophic nanoflagellates from photosyntheticprokaryotes represented 27% of the total amount of carbon obtainedfrom total prokaryotes     

Grazing by ciliates and heterotrophic nanoflagellates on picocyanobacteria in Lago Maggiore, Italy

During the oligotrophication of Lago Maggiore, picocyanobacteria(Pcy) increased in abundance and production. In their bimodal,seasonal cycle, the spring peak was due almost exclusively tosingle cells of Pcy, whereas in late-summer/autumn the varietyof morpho-types increased and larger Aphanothece-like rods appeared.Rates of Pcy cell removal by heterotrophic nanoflagellates andciliates were measured by using fluorescently labelled Pcy (FLC)in four experiments performed during the Pcy population shiftfrom small cocci to larger rods. The ciliate community appearedto be composed mainly of oligotrichs in the first two experiments,and subsequently of scuticociliates; heterotrophic nanoflagellatesdecreased in number from May to September, and there was a sizeshift which might reflect species composition change. Peritrichsemerged as the most efficient Pcy grazers. For the other ciliategroups we observed higher individual ingestion rates duringthe spring experiments than during those performed in late summer/autumn.The heterotrophic nanoflagellates ingested from 0.5 to3 Pcyh^-1 while ciliates ingested from 18 to 80 Pcy h^-1. The grazingimpact of the heterotrophic nanoflagellate community rangedfrom 1.9 x 10³ to 8 x 10³ Pcy ml^-1 h^-1, whereas the ciliatecommunity ingestion rate was one order of magnitude lower (0.2x 10³–0.4 x 10³ Pcy ml^-1 h^-1). A significant inverse correlationbetween Pcy size and the clearance rate of heterotrophic nanoflagellatesand ciliates was found. Our results indicate that protozoa areless efficient in cell uptake when the Pcy are composed of largercells. In Lago Maggiore, the carbon flux from Pcy to protozoadecreased from 29.8 to 10.2 µg C l^-1 day^-1 (May and Septemberrespectively). A tentative balance on an annual basis suggeststhat around 80% of the carbon produced by Pcy is taken up byprotozoa and channelled to metazooplankton.     

Microbial dynamics during the summer ice-loss phase in maritime Antarctic lakes

The dynamics of bacterioplankton and protozooplankton in twomaritime Antarctic lakes (Heywood Lake and Sombre Lake, SignyIsland, South Orkneys) were studied during the phase of icebreak-out (December and early January 1994/95). The lakes aresuffering animal-induced (fur seal) eutrophication, though HeywoodLake is most severely affected. Both lakes had morphologicallydiverse bacterial communities which increased during the studyperiod, reaching maxima of 80 x 10⁸ l^–1 in Heywood Lakeand 31.8 x 10⁸ l^–1 in Sombre Lake. Heterotrophic nanoflagellates(HNAN) reached a peak in late December with maxima of 40.6 x10⁸ l^–1 in Sombre Lake and 174 x 10⁵ l^–1 in HeywoodLake. Phototrophic nanoflagellates (PNAN) peaked in late Decemberafter ice loss in Heywood Lake (63 x 10⁵ l^–1), which coincidedwith a peak in a bloom of Chroomonas acuta which reached abundancesof 1.0 x 10⁸ l^–1. In Sombre Lake, ice persisted for alonger period and here PNAN reached their highest density atthe end of the study period (around 70.0 x 10⁵ l^–1). Ciliateabundance reached high levels in Heywood Lake (>60001^–1),while in Sombre Lake maximum abundance was 568l^–1. Protozooplanktondiversity was greater in the less-enriched Sombre Lake. Grazingrates of ciliates averaged 70.6 bacteria indiv.^–1 h^–1in Heywood Lake and 119.3 bacteria indiv.^–1 h^–1in Sombre Lake. The difference was a reflection of the differenttaxonomic make-up of the community in the lakes. HNAN grazingrates varied between 0.51 and 0.83 bacteria indiv.^–1 h^–1in Sombre and Heywood Lakes, respectively. Specific growth rates(r) h^–1 in Sombre Lake were 0.028 for ciliates and 0.013for HNAN, and in Heywood Lake 0.010 for ciliates and HNAN 0.012.These growth rates result in doubling times ranging between38 and 69 h for ciliates and around 55 h for HNAN.HNAN grazingon bacteria was curtailed in Heywood Lake in early January asa result of predation by microcrustacean larvae feeding on theplankton. Thus, for a short phase top-down control was apparentin the dynamics of Heywood Lake, a feature uncommon in Antarcticlake ecosystems. The impact of natural eutrophication on thesesystems is discussed in relation to other unaffected Antarcticlakes.     

Bacterivory in seawater samples estimated by a dual radioactive-labelling technique

A dual radioactive-labelled bacteria technique using Vibrio(DRLV), developed for laboratory studies on bacterivory, hasbeen refined for use at the concentrations of prey and predatorstypcially found at sea. Experiments with estuarine water collectedin spring and in autumn showed that bacterivorous nanoflagellates(HNF) (concentration 1.38±0.35x10³ HNF ml^–1) ingested2.7±0.96 DRLV flagellate1^–1 h^–1 at concentrationsof 0.8–2.2x10⁶ DRLV ml^–1 in the presence of 2.04±0.68x10⁶natural bacteria ml^–1. The method was also applied tosamples collected in October in the Celtic Sea, when on average1 ml of water from the surface layer contained 1.41±0.16x10⁶natural bacteria, 14.6x10³ cyanobacteria, 530±170 HNF,7.3±3.0x103 phototrophic nanoflagellates (1.5–4µm), 49.0±26.5 phototrophic dinoflagellates, 36.3±12.6heterotrophic dinoflagellates and 21.3±9.5 Leucocryptosmarina. Under these conditions the grazing rate in most samplesdid not exceed the coefficient of variation of the method (2%),although we estimate the grazing rate was -1.6 DRLV HNF^–1h^–1 and on one occasion a rate of 2.45 was recorded. Thegross growth efficiency for protein of -30% displayed by naturalHNF means that they could release about     

The dynamics of heterotrophic nanoflagellates and bacterioplankton in a large ultra-oligotrophic Antarctic lake

The abundance of both heterotrophic nanoflagellates (HNAN) andbacterioplankton in a large (9km²) ultraoligotrophic Antarcticlake (Crooked Lake) were investigated from December 1992 untilNovember 1993. HNAN abundance peaked in spring, summer and autumn,falling to lowest numbers during the winter. Numbers rangedbetween 0 and 50.9x10⁴ l^–1. Bacterioplankton abundancewas highest during the late summer and then fell progressivelytowards winter and autumn (range 1.19–4.46x10⁶ l^–1)In contrast to numbers, mean cell volumes (MCV) of the bacteriareached their highest in spring, and consequently highest bacterialbiomass occurred at this time. MCV ranged between 0.052 and0.224µm³. Bacterial production measurements followingthe incorporation of [³H] thymidine into DNA and [¹⁴C] leucineinto protein using a doubling-labelling procedure were undertakenin January, June, August, October and November. Rates variedbetween 2.8 and 52 ng C l¹ h¹. On occasions, a significant differencein production rates based on the uptake of leucine and thymidinewas observed, suggesting unbalanced growth. Highest rates ofproduction coincided with times of high dissolved organic carbonlevels in the water column and lowest production with low levelsof DOC. HNAN grazing rates were measured by following the uptakeof fluorescently labelled bacteria and averaged 4.8 bacterialcells individual¹ day¹ at 2 and 4°C. Specific growth rates(h¹) ranged around 0.00070–0.00077 in both the field andlaboratory, giving doubling times of 37.3 and 41.0 days, respectively.These low rates of grazing and growth indicate that there isno adaptation to low temperatures in these freshwater protists.Based on these data, the gross production efficiency is 24%.HNAN removed between 0.1 and 9.7% of bacterial production perday.     

Nanoheterotroph grazing on bacteria and cyanobacteria in oxic and suboxic waters in coastal upwelling areas off northern Chile

The vertical distribution and abundance of microbial assemblagesand the grazing of nanoheterotrophs upon prokaryotes in oxicand suboxic waters were examined in two coastal upwelling areasoff northern Chile where a shallow Oxygen Minimum Zone (OMZ)is characteristic. Prokaryotic prey included bacterioplanktonand cyanobacteria (Synechococcus); both displayed a bimodaldistribution, with abundance maxima above and within the upperOMZ. Flagellates numerically dominated the nanoplankton andwere mostly concentrated in the oxic layer. Mean ingestion ratesof cyanobacteria by nanoflagellates (vacuole content method)ranged from 0.2 to 1.1 cells flagellate^–1 h^–1 andmean consumption rates (34–160 cells mL^–1 h^–1)were four times higher in the oxic layer. With the selectiveinhibitors technique, specific grazing rates on bacteria werelow (<0.1 h^–1) and consumption did not control bacterialproduction in the surface layer but did so in the suboxic layer(accounting for >100% of bacterial production). With thesame method, the specific grazing rate on cyanobacteria rangedbetween zero and 0.23 h^–1 with no clear differences betweenoxygen conditions; prey growth and production were always higherthan the grazing pressure (accounting for <17% of cyanobacterialproduction). The impact of grazing by nanoheterotrophs in regulatingthe production of prokaryotes in oxic and suboxic waters inthis region is discussed.     

Microbial Food Webs in Marine Sediments. I. Trophic Interactions and Grazing Rates in Two Tidal Flat Communities

Abstract The role of grazing by marine sediment flagellates, ciliates, and meiobenthic animals in controlling production of their bacterial and diatom prey was investigated. Several novel or modified techniques were used to enumerate prey (bacteria and diatoms), measure bacterial production, quantify proto- and micrometazoan predators, and evaluate rates of bacterivory and herbivory. The results indicated that, in a temperate, marine intertidal flat composed of fine sand, colorless nanoflagellates, ciliates, and nematodes were the most important bacterivores. Together, these organisms were responsible for removing up to 53% of bacterial production, by grazing. The observed rates of bacterivory were high enough to hypothesize that periods of grazing control of bacterial production might occur regularly in similar habitats. Colorless microflagellates, ciliates, and nematodes had high rates of diatom consumption. The combined small diatom consumption rate was equivalent to 132% of diatom standing stock per day. Trophic interactions between diatoms and micro- and meiobenthos might be a factor limiting growth of small (around 10 μm) diatoms. In coarse sands of an open beach, all micrograzers except pigmented nanoflagellates were rare, whereas bacterial and diatom assemblages were rather abundant and active. In this type of sediment, the micrograzers were able to consume only a marginal percentage of bacterial production (<1%) and diatom standing stock (3.8%), thus playing a minor role in controlling the dynamics of their prey. Received: 11 June 1996; Accepted: 13 August 1996     

Dynamic characteristics of Prochlorococcus and Synechococcus consumption by bacterivorous nanoflagellates

We compared the characteristics of ingestion of Prochlorococcus and Synechococcus by the marine heterotrophic nanoflagellate Pseudobodo sp. and by a mixed nanoflagellate culture (around 3 microm in size) obtained from an open sea oligotrophic area. Maximum ingestion rate on Synechococcus (2.7 Syn flagellate(-1) h(-1)) was reached at concentrations of 5 x 10(5) Syn mL(-1) and decreased between 6 x 10(5) and 1.5 x 10(6) Syn mL(-1). In order to validate laboratory data, one set of data on Synechococcus grazing was obtained during a field study in the oligotrophic northeastern Mediterranean Sea. Ingestion rates by heterotrophic nanoflagellates were related to Synechococcus abundance in the water, and the feeding rate showed a clear diel rhythm with consumption being highest during the night, declining during the day hours, and being lowest at dusk. Ingestion rates on Prochlorococcus increased linearly for the whole range of prey density used (i.e., from 1 x 10(3) to 3 x 10(6) Proc mL(-1)), with maximum ingestion of 6.7 Proc flagellate(-1) h(-1). However, for prey concentrations in the range of 10(3)-10(5), which are usually encountered in aquatic systems, ingestion rates were significantly less than on Synechococcus. In our experiments, both Prochlorococcus and Synechococcus proved to be poor food items for support of nanoflagellate growth.     

Laboratory-measured grazing and ingestion rates of the salp, Thalia democratica Forskal, and the doliolid, Dolioletta gegenbauri Uljanin (Tunicata, Thaliacea)

Grazing and ingestion rates of laboratory-born Thalia democraticaaggregates and Dolioletta gegenbauri gonozooids, phorozooidsand oozooids were determined while fed Isochrysis galbana (4–5µm diameter) alone or in combination with Peridinium trochoideum(16–18 µm diameter) at concentrations of 0.15–0.70mm³ x 1^–1. Grazing rates (ml x zooid^–1 x 24 h ^–1)ranged from 10 to 355, and at zooid weights greater than 5 µgcarbon were in order oozooid > gonozooid > aggregate.Grazing rates increased exponentially with increasing zooidweight. Weight-specific grazing rates (ml x µgC^–1x 24 h^–1) were independent of the four-fold initial foodconcentration. Mean weight-specific grazing rates increasedlinearly with increasing zooid weight for the aggregates andoozooids, but gonozooid mean rates were independent of zooidweight. Aggregate and gonozooid ingestion rates (10⁶ µm³x zooid^–1 x 24 h^–1) ranged from 4 to 134 while oozooidrates ranged from 3 to 67. All ingestion rates were independentof the initial food concentration but increased linearly withincreasing zooid weight at similar rates. All mean weight-specificingestion rates (ml x µgC^–1 x 24 h^–1) wereindependent of zooid weight. The mean aggregate daily ration(µgC ingested x µg body C^–1) was 59% and themean doliolid ration was 132%. Field studies indicate that normalconcentrations of D. gegenbauri in the Georgia Bight clear theirresident water volume (1 m³) in about 4 months, but that highlyconcentrated, swarm populations which occur along thermohalinefronts clear their resident water volume in less than 1 day. ¹Current address: MacLaren Plansearch Ltd., P.O.Box 13250, sta.A.,St.John's, Nfld. A1B 4A5     

Grazing on bacteria by flagellates and cladocerans in lakes of contrasting food-web structure

We tested the hypothesis that grazing on bacteria would varybetween lakes with differing plankton community structures.Paul and Tuesday lakes (Gogebic County, MI) are respectivelydominated by piscivorous and planktivorous fish. Consequently,zooplankton in Paul are primarily large daphnids, while zooplanktonin Tuesday are primarily small cladocerans and copepods. Wemeasured flagellate grazing on bacteria using a fluorescentminicell method, while cladoceran grazing was estimated fromthe relationship between body length and filtering rate. Wepredicted that cladoceran grazing on bacteria would be higherin Paul, and flagellate grazing would be higher in Tuesday.Cladoceran grazing on bacteria was important in both lakes contraryto our initial expectation. Large populations of the small cladoceran,Bosmina longirostris, in Tuesday exerted a grazing pressure(0.18–35x10⁶ bacteria 1^–1 h^–1) approximatelyequal to that of the large cladoceran, Daphnia pulex, in Paul(0.34–30x10⁶ bacteria 1^–1 h^–1). Flagellategrazing was higher in Tuesday as predicted (range: Paul, 0.1–6x10⁶bacteria 1^–1 h^–1; Tuesday, 0.2–20x10⁶ bacteria1^–1 h^–1). However, there was not a simple relationshipbetween total abundance of flagellates and total grazing rates.High community grazing by flagellates occurred when attachedchoanoflagellates were present. These flagellates had higheringestion rates than free forms. We find no clear evidence thatdifferences in food-web structure between the two lakes influencethe process of grazing on bacteria. Instead, our results emphasizethe significance of cladocerans and attached flagellates asconsumers of bacteria in freshwater ecosystems.     

Indirectly fluorescently labelled flagellates (IFLF): a tool to estimate the predation on free-living heterotrophic flagellates

A procedure was developed to estimate the direct grazing impacton free-living heterotrophic nanoflagellates (HNF). Culturedflagellates were labelled by feeding on brightly fluorescingbacteria (FLB) and then offered as indirectly fluorescentlylabelled flagellates (IFLF) to potential predators of HNF. Thenumber of FLB in the predators' food vacuoles could be convertedinto IFLF uptake and consumption of HNF. This new techniquewas used to study the HNF-ciliate relationship in the pelagiczone of Lake Constance. Three groups of ciliates were detectedas HNF grazers: small representatives of the genus Strobilidium.a small Haltena-like ciliate (probably Halteria grandinella)and a Codonella sp. Tintinnidium sp. group The ingestion ofHNF by these groups of ciliates ranged between 3 and 15, 3 and39, and 3 and 7 HNF ciliate^–1 h^–1; respectively.The IFLF method allows the direct determination of ingestedflagellate prey in the food vacuoles of their predators. Becauseindigenous living prey organisms were used, tracer discriminationcan be reduced.     

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.     

Bacterial growth and losses due to bacterivory in a mesotrophic lake

Bacterial secondary production and rates of bacterivory weredetermined from samples collected from mesotrophic Lake Arlington.Bacterial production and losses were determined by comparingthe growth of natural bacterial assemblages in the presenceof predators (unfiltered samples) to growth in the absence ofpredators (water filtered through 1.0 (im porosity filters).Growth rates of heterotrophic nanoflagellates (HNF) were estimatedfrom growth in the absence of predators (water filtered through5.0 µm porojity filters). Bacterial growth rates rangedbetween 0.002 and 0.069 h^–1 and averaged 0.026 h^–1.HNF grew at rates ranging between 0.003 and 0.107 h^–1and averaged 0.028 h^– Grazing rates ranged between 0.002and 0.043 h^–1, and averaged 0.018 h. The annual averagerate of bacterial biomass synthesis was 3.2 –g Cl^–h^–1 and {small tilde}69% of this production was grazed.Temporal changes in growth and grazing rates suggest a tightlycoupled predator-prey linkage in this lake. ¹Present address: Hydrobiological Institute, Czech Academy ofSciences, Na sddkach 7, 370 05 teski Budjovice, Czech Republic     

Complex interactions and different possible pathways among functional components of the aquatic microbial world in Farasan Archipelago,Southern Red Sea,Saudi Arabia

This work aims to outline the dynamics of trophic links between the three main microbial components (bacteria, nanoflagellates, and ciliates) of the Farasan Archipelago in order to establish a baseline for future research in this area. The Farasan Archipelago lies along the southwestern coast of the Saudi Arabia, southern Red Sea between 16°20′–17°10′N and 41°30′–42°30′E and had been declared as marine and terrestrial reserve by the year 1996. Three different sites were chosen for this study, with each site visited bimonthly for 18 months from September 2016 to February 2018. Bacteria, nanoflagellates and ciliates were enumerated in order to explore the complex interactions between the main microbial categories in sea waters of the Farasan Archipelago. High abundances were recorded during the present study for bacteria (8.7 × 10⁶ bacteria ml⁻¹), nanoflagellates (3.7 × 10⁴ TNAN ml⁻¹) and ciliates (40.4 ciliates ml⁻¹). The paper discusses the various potential pathways controlling the complex interactions between these microbial groups in this part of the southern Red Sea. It is concluded that a linear trophic chain consisting of bacteria; heterotrophic nanoflagellates; filter feeding ciliates is a major route by which the production of bacteria is transferred to the higher consuming levels, thereby confirming the high importance of t bottom-up control (food supply), alongside top-down control (predation) in regulating bacterial abundances in the Farasan Archipelago. During the present investigation, each nanoflagellate ingested between 11 and 87 bacteria in one hour, while each ciliate consumed between 20 and 185 nanoflagellates every hour. These calculated grazing rates of protistan eukaryotes confirmed the role of heterotrophic nanoflagellates as the main consumers of bacteria, and the role of ciliates as the major control for the heterotrophic nanoflagellate population dynamics, and thus the top predators within the microbial plankton assemblage in the Farasan Archipelago.     

Pigment-specific rates of phytoplankton growth and microzooplankton grazing in a subtropical lagoon

Phytoplankton growth and microzooplankton grazing rates wereevaluated in one station in Bahía Concepción,located in the middle region of the Gulf of California, México.We used high-performance liquid chromatography (HPLC) estimationsof phytoplankton pigment signatures to evaluate the annual variationof taxon-specific grazing and growth rates obtained with thedilution technique. Chlorophyll-a (Chl-a) concentrations variedwidely (0.34–3.32 µg L^–1) and showed two maxima,during late spring and autumn, associated with the transitionbetween mixed and stratified conditions. Phytoplankton growthrates varied seasonally with the lowest rates during summer(range: 0.01–2.55 day^–1 for Chl-a; 0.00–3.84day^–1 for Chl-b; 0.26–3.29 day^–1 for fucoxanthin;0.00–6.27 day^–1 for peridinin; 0.00–4.35 day^–1for zeaxanthin). Microzooplankton grazing was an important lossprocess (range: 0.0–1.89 day^–1 for Chl-a; 0.00–3.12day^–1 for Chl-b; 0.26–3.29 day^–1 for fucoxanthin;0.00–2.03 day^–1 for peridinin; 0.00–3.51 day^–1for zeaxanthin). Average grazing rates accounted 68–89%of estimated average phytoplankton pigment-specific growth rates.The analysis of pigment signatures indicates that diatoms anddinoflagellates were the dominant groups, and contrary to expectationfor typical subtropical lagoons, the specific growth rates inBahía Concepción showed a pronounced seasonalvariability, linked to transitional hydrographic conditions.Our results indicate a close coupling between the communitymicrozooplankton grazing and phytoplankton growth rates, withoutselective feeding behavior. These results suggest that microzooplanktonplay a critical role and may significantly modify the availabilityand efficiency of transfer of energy to higher trophic levels.     

Abundance, frequency of dividing cells and growth rates of Synechococcus sp. (cyanobacteria) in the stratified Northwest Mediterranean Sea

The abundance, frequency of dividing cells and growth ratesof the planktonic cyano bacteria Synechococcus sp. during thesummer of 1995 and 1996 were estimated in the Northwest MediterraneanSea to test whether depth-dependent growth rates of this speciesexplain its dominance in the deep chlorophyll maximum (DCM)layer formed during summer thermal stratification in the NWMediterranean, compared to the surface layer. Abundance at theDCM layer (50–70 m) was up to two orders of magnitudegreater than that at the surface, with values ranging from 1.7to 13x10⁶ cells I-¹ and from 4 to 175 x 10⁶ cells I-¹ at thesurface and in DCM waters, respectively. Gross growth rates,however, were much higher at the surface than in the DCM layer(surface: 0.76–1.07 day DCM: 0.30–0.47 day-¹ Thehigher gross growth rates at the surface layer were supportedby a higher frequency of dividing cells (surface: 0.09–0.24;DCM: 0.01–0.12). The negative correlation between theabundance or standing stock and growth rates of these planktonicpicocyanobacteria points to losses, and not growth rate, asthe main control on the abundance of Synechococcus. Althoughwe provide some evidence that grazing alone may be able to accountfor these losses, further, direct determinations are clearlyneeded to elucidate the regulation of the abundance of Synechococcusin the NW Mediterranean.     

Dynamics of microplankton communities at the ice-edge zone of the Lazarev Sea during a summer drogue study

Microzooplankton grazing and community structure were investigatedin the austral summer of 1995 during a Southern Ocean Drogueand Ocean Flux Study (SODOFS) at the ice-edge zone of the LazarevSea. Grazing was estimated at the surface chlorophyll maximum(5–10 m) by employing the sequential dilution technique.Chlorophyll a concentrations were dominated by chainformingmicrophytoplankton (>20 µm) of the genera Chaetocerosand Nitzschia. Microzooplankton were numerically dominated byaloricate ciliates and dinoflagellates (Protoperidinium sp.,Amphisoleta sp. and Gymnodinium sp.). Instantaneous growth ratesof nanophytoplankton (<20 µm) varied between 0.019and 0.080 day^–1, equivalent to between 0.03 and 0.12 chlorophylldoublings day^–1. Instantaneous grazing rates of microzooplanktonon nanophytoplankton varied from 0.012 to 0.052 day^–1.This corresponds to a nanophytoplankton daily loss of between1.3 and 7.0% (mean = 3.76%) of the initial standing stock, andbetween 45 and 97% (mean = 70.37%) of the daily potential production.Growth rates of microphytoplankton (>20 µm) were lower,varying between 0.011 and 0.070 day^–1, equivalent to 0.015–0.097chlorophyll doublings day^–1. At only three of the 10 stationsdid grazing by microzooplankton result in a decrease in microphytoplanktonconcentration. At these stations instantaneous grazing ratesof microzooplankton on microphytoplankton ranged between 0.009and 0.015 day^–1, equivalent to a daily loss of <1.56%(mean = 1.11%) of initial standing stock and <40% (mean =28.55%) of the potential production. Time series grazing experimentsconducted at 6 h intervals did not show any diel patterns ofgrazing by microzooplankton. Our data show that microzooplanktongrazing at the ice edge were not sufficient to prevent chlorophylla accumulation in regions dominated by rnicrophytoplankton.Here, the major biological routes for the uptake of carbon thereforeappear to be grazing by metazoans or the sedimentation of phytoplanktoncells. Under these conditions, the biological pump will be relativelyefficient in the drawdown of atmospheric CO₂.     

An approach to measure ciliate grazing on living heterotrophic nanoflagellates

The complicated routes by which organic material is channelled up to higher trophic levels via bacteria and protozoans is a major issue in aquatic microbial ecology. Because of the fragile nature of protists it is not straightforward to perform experimental studies of prey–predator interactions. Here we present an approach for the assessment of ciliate grazing on living heterotrophic nanoflagellates. Stationary phase cultures of a heterotrophic nanoflagellate (Cafeteria sp.) were live-stained by allowing them to take up fluorescently labelled macromolecules. Controls revealed that this label persisted for several hours. Fluorescently labelled living flagellates (FLLF) were added into enriched natural assemblages of marine oligotrich ciliates and uptake of FLLF was monitored over time. Oligotrich ciliates did not incorporate fluorescent-labelled macromolecules but a linear FLLF uptake over time was observed for 20–30 min at 20°C. Ingestion rates were 21–46 FLLF h^–1 at a concentration of about 2×10⁴ FLLF ml^–1, which corresponded to clearance rates of 0.7–0.8 l ciliate^–1 h^–1. These results are in the same order of reported ciliate grazing on phytoplankton of similar size. This method represents a direct approach to measure ciliate grazing specifically on living heterotrophic nanoflagellates.     

Photo- and heterotrophic pico- and nanoplankton in the Mississippi River plume: distribution and grazing activity

The abundance of pico- and nanophytoplankton, bacteria and heterotrophicnanoflagellates, and grazing rates on phototrophic pico- andnanoplankton and bacterioplankton were assessed along a salinitygradient (0.2–34.4) in the Mississippi River plume inMay 2000. Grazing rates were established by serial dilutionexperiments, and analysis by flow cytometry allowed differentiationof grazing rates for different phytoplankton subpopulations(eukaryotes, Synechococcus spp., Prochlorococcus spp.). Grazingrates on phytoplankton tended to increase along the salinitygradient and often approached or exceeded 1 day^-1. Phytoplanktonnet growth rates (growth – grazing) were mostly negative,except for positive values for eukaryotic nanoplankton in thelow-salinity, high-chlorophyll region. Grazing pressure on bacteriawas moderate (     

Dynamics of autotrophic picoplankton in Lake Constance

The vertical distribution, biomass concentrations and growthrates of autotrophic picoplankton (APP) were investigated duringthe growing season (March-October) in Lake Constance in differentdepths. Cell numbers determined by epifluorescence microscopyvaried between 1.0 x 10³ and 1.6 times; 10⁵ cells ml^–1depending on season and water depth. Highest concentrationswere recorded above the thermodine in late summer. Numerically,APP consisted almost exclusively of chroococcoid cyanobactena.During lake stratification several peaks of biomass concentrationsoccurred in epilimsietic waters at intervals of 6–8 weeks.In-situ experiments using a dilution technique and dialysisbags revealed that during summer APP population dynamics wereprimarily driven by combined changes of their growth and grazingrates, whereas temperature was less important. Gross growthrates varied between 0.006 and 0.051 h^–1, grazing ratesbetween 0.002 and 0.053 h^–1. On average APP productionwas completely removed by grazing within the microbial community.Ciliates, heterotrophic nanoflagellates and rotifers have beenidentified as the major consumers of APP cells. APP biomassis small compared to larger phytoplankton, ranging from ito5% of total phytoplankton biovolume. Due to its high gross growthrates, which are on the same level as those of free-living pelagicbacteria, APP contributes slightly more to overall primary productionwith maximum percentages of {small tilde}15% in late summer.