Comparative growth rates and yields of ciliates and heterotrophic dinoflagellates

Growth rates, ingestion rates and grazer yields (grazer volumeproduced/prey volume consumed) were measured for six protozoanspecies (ciliates: Favella sp., Strombidinopsis acuminatum,Uronema sp.; heterotrophic dinoflagellates: Amphidinium sp.,Gymnodinium sp., Noctiluca scintillans) in laboratory batchculture experiments. Comparative growth data indicate that theprymnesiophyte Isochrysis galbana, the prasinophyte Mantoniellasquamata, two cryptophyte species and several autotrophic dinoflagellatespecies were suitable foods for these grazers. When grown onoptimized diets at 13C, maximum ciliate growth rates (range0.77–1.01 day^–1 uniformly exceeded maximum heterotrophicdioflagellate growth rates (range 0.41–0.48 day^–1).A compilation of published data demonstrates that this growthrate difference persists across a range of ciliate and dinoflagellatetaxa and cell sizes. Comparison of volume-specific ingestionrates and yields for the six species studied here showed thatthere was no single explanation for this growth rate disparity.Heterotrophic dinoflagellates exhibited both low ingestion ratesand, in one case, low yields; ciliates were able to achievehigher growth rates via either higher ingestion rates or higheryields, depending on ciliate species. Volume yield increasedover time throughout the exponential growth phase in nearlyall experiments, suggesting variation in response to changingfood concentrations or long-term acclimation to culture conditions.Higher maximum ciliate growth rates mean that these grazershave the potential to exercise tighter control over incipientblooms of their prey than do heterotrophic dinoflagellates.     

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

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

Phosphorus gain by bacterivory promotes the mixotrophic flagellate Dinobryon spp. during re-oligotrophication

Bacterivory by mixotrophic flagellates may contribute to theirnutrient supply, providing a competitive advantage in oligotrophicwaters. We hypothesized an increase in Dinobryon biomass duringthe re-oligotrophication process in the large and deep LakeConstance. To estimate whether bacterivory contributed substantiallyto the flagellates’ phosphorus supply, we determined ingestionrates. Dinobryon biomass increased with decreasing total phosphorusconcentrations in the lake over a period of 17 years (P = 0.0005).The promotion of Dinobryon biomass during re-oligotrophicationmay be explained by the increasing light availability due tothe decreasing biomass of other phytoplankton yielding a releasefrom competition. The date of the Dinobryon abundance maximumshifted to earlier time points in the year, probably becausea smaller phosphorus pool was depleted more quickly. Ingestionrates of Dinobryon ranged between 0.5 and 13 bacteria cell^–1h^–1 (0.2–5.4 fg C pg C^–1 h^–1), and clearancerates varied between 0.2 and 3.2 nL cell^–1 h^–1 (4–78pL pg C^–1 h^–1), leading to bacterial losses of upto 30% day^–1 of bacterial standing stock. The ingestionof bacteria covered 77% of the phosphorus need of the flagellateduring the period of maximum growth in 1996 (net growth rate0.34 day^–1), and it fully covered the need at all othertimes.     

Dynamics of herbivorous grazing by the heterotrophic dinoflagellate oxyrrhis marina

In a series of batch experiments in the dark the heterotrophicdinoflagellate Oxyrrhis marina grazed three phytoplankton prey(Phaeodactylun tricornutum, Isochrysis galbana and Dunaliellateriolecta) with equal efficiency. Growth rates of the dinoflagellateranged between 0.8 and 1.3 day–1 Maximum observed ingestionrates on a cell basis varied according to the size of the preyfrom about 50 cells flagellate^–1 day^–1 when D.tertiolectawas the prey to 250–350 cells fiagellate^–1 day^–1when the other species were eaten. However, when compared ona nitrogen basis, ingestion rates were independent of prey type.Both ingestion and growth ceased when prey cell concentrationsfell below a threshold concentration of about 10⁵ cells ml^–1.Maximum specific clearance rates were 0.8x10⁴0ndash;5.7x10⁴it day which is considerably lower than that found for heterotrophicdinoflagellates in oceanic waters and may explain why O.marinagenerally thrives only in productive waters. The timing of NHregeneration was linked to the C:N ratio of the prey at thestart of grazing. Regeneration efficiencies for NH₄. never exceeded7%; during the exponential phase and were 45% well into thestationary phase. These results are comparable to those obtainedwith heterotrophic flagellates and demonstrate that the bioenergeticpatterns of grazing and nutrient cycling by different protozoaare very similar. Moreover, they support the notion that toachieve 90+% nutrient regeneration in the open ocean, as iscurrently believed, the microbial food loop must consist ofmultiple feeding steps. Alternatively, nutrient regenerationefficiencies may be considerably lower than 90%.     

Effects of salinity and two coastal waters on the growth and toxin content of the dinoflagellate Alexandrium minutum

The dinoflagellate Alexandrium minutum strain AM89BM was studiedto investigate its capacity to adapt to different salinitiesand the influence of salinity on cellular content of paralyticshellfish toxins (PST), in batch culture in enriched offshoreseawater media. The strain shows optimal growth (average rate=" BORDER="0">0.5 div day^-1) at salinities between 20 and 37p.s.u., peaking at 25 p.s.u. (0.63 ± 0.07 div day^-1).Under a high NO₃^–:PO₄^3– mole ratio (76), cell PSTcontent increased during growth phase, peaking toward the endof growth phase or in the early stationary phase. The PST contentwas low (10 fmol PST cell^-1) from 30 to 37 p.s.u., but it increasedat lower salinities, with the maximum value (50 fmol PST cell^-1)recorded at 15 p.s.u. We then compared growth rate and toxincontent of A. minutum cells grown in 3- and 0.2-µm filteredestuarine water (27 p.s.u.), and a similarly filtered seawatercollected from an oyster farming area (36 p.s.u.), with a N-and P-enriched offshore seawater (37 p.s.u.). In both estuarinewater treatments, growth was fast (=" BORDER="0">0.8 div day^-1)and the cell PST content increased only in the early growthphase, peaking in mid-growth phase at 9.56 ± 1.06 and7.63 ± 0.44 fmol PST cell^-1 in the 3- and 0.2-µmfiltered waters, respectively. In the 3-µm filtered oysterfarm water, although inorganic nutrient concentrations werevery low, A. minutum grew well (0.68 ± 0.06 div day^-1),suggesting mixotrophic nutrition; as PST production was nearlyzero, the cell toxin content decreasing to 1.11 fmol PST cell^-1,we hypothesize that toxin biosynthesis was greatly weakeneddue to the lack of amino acid precursors in prey material. Inthe offshore seawater, A. minutum grew slowly (0.18 ±0.04 div day^-1) and cells lost toxins down to 1.08 fmol PSTcell^-1, suggesting that growth was limited and PST productionstopped due to the lack of some vitamins, and/or trace metals.     

Biomass and lipid productivities of <Emphasis Type="Italic">Chlorella vulgaris</Emphasis> under autotrophic,heterotrophic and mixotrophic growth conditions

Biomass and lipid productivities of Chlorella vulgaris under different growth conditions were investigated. While autotrophic growth did provide higher cellular lipid content (38%), the lipid productivity was much lower compared with those from heterotrophic growth with acetate, glucose, or glycerol. Optimal cell growth (2 g l⁻¹) and lipid productivity (54 mg l⁻¹ day⁻¹) were attained using glucose at 1% (w/v) whereas higher concentrations were inhibitory. Growth of C. vulgaris on glycerol had a similar dose effects as those from glucose. Overall, C. vulgaris is mixotrophic.     

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.     

Seasonal photosynthetic activity of autotrophic picoplankton in Lake Kinneret, Israel

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

Feeding and metabolism of the siphonophore Sphaeronectes gracilis

The in situ predation rate of the siphonophore Sphaeronectesgracilis was estimated from gut content analysis of hand-collectedsiphonophores and from laboratory data on digestion rates ofprey organisms. At daytime prey densities of 0.25 copepods 1^–1,S. gracilis was estimated to consume 8.1 – 15.4 prey day^–1siphonophore^–1. From data on abundances of siphonophoresand copepods, S. gracilis was estimated to consume 2–4%of the copepods daily. In laboratory experiments, ingestionrates averaged 13.8 prey day^–1 siphonophore^–1 atprey densities of 5 copepods 1^–1 and 36.9 at 20 copeods1^–1. This was equivalent to a specific ingestion rate(for both carbon and nitrogen) of –17% day^–1 and45% day^–1, respectively, while specific ingestion in situwas only 2% day^–1. Ammonium excretion averaged 0.095 µg-atsiphonophore^–1 day^–1 at 5 prey 1^–1, and 0.162at 20 prey 1^–1. The specific respiration (carbon) andspecific excretion (nitrogen as ammonium) were calculated tobe 3% day^–1 at the lower experimental food level, and5% day^–1 at the higher food level. ¹Contribution from the Catalina Marine Science Center No. 66. ²Present address: Dept. of Biology, University of Victoria,Victoria, B.C., Canada V8W 2Y2.     

Growth and production of heterotrophic nanoflagellates in a meso-eutrophic lake

The growth of heterotrophic nanoflagellates (HNF) in mesotrophicLake Constance was measured in situ during a 13 month period.Experiments were conducted with 10 µm pre-filtered lakewater incubated in diffusion chambers at 3 m water depth atthe sampling location for 24 h. Growth rates were calculatedfrom changes in cell numbers occurring during the period ofincubation. Growth rates of all dominant taxa showed pronouncedseasonal variation (–0.13 to 1.76 day^–1 and weregenerally highest in summer at high water temperatures. In situgrowth rates were well below maximum growth rates known forthe respective and similar species from laboratory experiments.While water temperature was a key parameter positively relatedto the growth of all HNF species, the effect of various potentialfood items was taxon specific and less clear. Bacterial abundancewas equally important as temperature for growth in the smallbactenvorous Spumella sp., but was insignificant for growthrates of the larger omnivorous Kathablepharis sp. In Spuniellasp., 84% of the observed seasonal variation of its growth ratecould be explained by temperature and bacterial food supply.Based on these results, a multiple linear regression equationwith temperature and bacterial concentration as dependent variableswas calculated for the growth rate of Spumella. Taxon-specificproduction rates were derived from growth rates and averagebiomass of these two species, and compared to total HNF productionestimated from previously measured community growth rates andbiomass in Lake Constance. Production peaks of Spumella sp.and Kathablepharis sp. alternated seasonally. Total HINF productionranged from –0.01 to 10 mg C m^–3 day^–1. Theaverage seasonal production varied between 1.4 and 33 mg C m^–3day^–1 over 6 consecutive years. These small protozoa thuscontribute a substantial amount to total zooplankton productionin Lake Constance.     

Trophodynamics of the scyphomedusae Aurelia aurita. Predation rate in relation to abundance, size and type of prey organism

Ephyra larvae and small medusae (1.7–95 mm diameter, 0.01–350mg ash-free dry wt, AFDW) of the scyphozoan jellyfish Aureliaaurita were used in predation experiments with phytoplankton(the flagellate Isochrysis galbana, 4 µm diameter, {smalltilde}6 x 10^–6 µg AFDW cell^–1), ciliates (theoligotrich Strombidium sulcatum, 28 µm diameter, {smalltilde}2 x 10^–3 µg AFDW), rotifers (Synchaeta sp.,0.5 µg AFDW individual^–1) and mixed zooplankton(mainly copepods and cladocerans, 2.1–3.1 µg AFDWindividual^–1). Phytoplankton in natural concentrations(50–200 µg C I^–1) were not utilized by largemedusae (44–95 mm diameter). Ciliates in concentrationsfrom 0.5 to 50 individuals ml^"1 were consumed by ephyra larvaeand small medusae (3–14 mm diameter) at a maximum predationrate of 171 prey day^–1, corresponding to a daily rationof 0.42%. The rotifer Synchaeta sp., offered in concentrationsof 100–600 prey I^–1, resulted in daily rations ofephyra larvae (2–5 mm diameter) between 1 and 13%. Mixedzooplankton allowed the highest daily rations, usually in therange 5–40%. Large medusae (>45 mm diameter) consumedbetween 2000 and 3500 prey organisms day^"1 in prey concentrationsexceeding 100 I^–1. Predation rate and daily ration werepositively correlated with prey abundance. Seen over a broadsize spectrum, the daily ration decreased with increased medusasize. The daily rations observed in high abundance of mixedzooplankton suggest a potential ‘scope for growth’that exceeds the growth rate observed in field populations,and this, in turn, suggests that the natural populations areusually food limited. The predicted predation rate at averageprey concentrations that are characteristic of neritic environmentscannot explain the maximum growth rates observed in field populations.It is therefore suggested that exploitation of patches of preyin high abundance is an important component in the trophodynamicsof this species. ¹Present address: University of Bergen, Department of MarineBiology, N-5065 Blomsterdalen, Norway     

Use of the 'Food Vacuole Content' Method to Estimate Grazing by the Mixotrophic Dinoflagellate Gyrodinium Galatheanum on Cryptophytes

We measured in situ grazing rates of the mixotrophic dinoflagellateGyrodinium galatheanum (Braarud) Taylor 1995 on populationsof phycoerythrin-containing cryptophytes in Chesapeake Bay.Rates were estimated from instantaneous food vacuole contents,in situ temperatures, cryptophyte abundances and experimentallydetermined digestion rates. Laboratory digestion experimentsshowed that specific digestion rate constants increased sigmoidallywith temperature, but were unrelated to the initial food vacuolecontent when it was <0.46 cryptophytes dinoflagellate^–1.These results allowed us to establish an empirical model toestimate in situ ingestion of cryptophyte prey by G. galatheanum.The estimated rates ranged from 0 to 0.26 cryptophytes dinoflagellate^–1day^–1, corresponding to daily ingestion of 0–12.29pg carbon, 0–2.48 pg nitrogen and 0–0.34 pg phosphorusdinoflagellate^–1. Estimated daily consumption of cryptophytebiomass by G. galatheanum was equivalent to 0–12% of bodycarbon, 0–13% of body nitrogen and 0–21% of bodyphosphorus. Estimated in situ clearance rates for cryptophytesranged from 0 to 0.27 µl dinoflagellate^–1 day^–1,representing daily removal of 0–4% of the cryptophytestanding stock. Although G. galatheanum may increase its growthrate through phagotrophy, it appears to have little grazingimpact on cryptophyte prey populations.     

Mixotrophic organisms become more heterotrophic with rising temperature

The metabolic theory of ecology predicts that temperature affects heterotrophic processes more strongly than autotrophic processes. We hypothesized that this differential temperature response may shift mixotrophic organisms towards more heterotrophic nutrition with rising temperature. The hypothesis was tested in experiments with the mixotrophic chrysophyte Ochromonas sp., grown under autotrophic, mixotrophic and heterotrophic conditions. Our results show that (1) grazing rates on bacterial prey increased more strongly with temperature than photosynthetic electron transport rates, (2) heterotrophic growth rates increased exponentially with temperature over the entire range from 13 to 33 °C, while autotrophic growth rates reached a maximum at intermediate temperatures and (3) chlorophyll contents during mixotrophic growth decreased at high temperature. Hence, the contribution of photosynthesis to mixotrophic growth strongly decreased with temperature. These findings support the hypothesis that mixotrophs become more heterotrophic with rising temperature, which alters their functional role in food webs and the carbon cycle.     

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

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

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.     

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.     

Growth and feeding rates of the newly hatched larval ctenophore Mnemiopsis leidyi A. Agassiz (Ctenophora, Lobata)

Mnemiopsis leidyi: larvae depend on microplankton (<200 µm) prey duringthe first few days following hatching until larvae are >0.5mm in length and can successfully capture and consume mesozooplanktonprey. Feeding and growth rates of newly hatched M. leidyi larvaewere measured in controlled laboratory experiments. When fednatural microplankton assemblages, newly hatched larvae consumedsignificant quantities of both autotrophic and heterotrophicprey, including diatoms, phototrophic, heterotrophic and mixotrophicdinoflagellates, euglenoid flagellates, aloricate and tintinnidciliates, and rotifers. Average per capita clearance rates were1.99–7.59 mL individual^–1 h^–1 ( = 4.01 mL individual^–1 h^–1; SD = 1.95)and total per capita ingestion was 0.01–4.70 µgC individual^–1 day^–1 x 10² ( = 0.83 µg C individual^–1 day^–1 x 10²; SD =1.89). Larval growth rates were –0.13 to 0.56 mm individual^–1day^–1 (equivalent to –1.72 to 4.33 µg C individual^–1day^–1) over a range of larval sizes from 0.5 (<0.5µg C) to 5 mm (85 µg C). A diet consisting entirelyof microplankton prey supported larval growth for >2 weeks,and growth rate decreased when larvae reached 4–5 mm inlength, corresponding to the beginning of their morphologicaltransition from tentaculate to lobate feeding mode. The grossgrowth efficiency of larvae fed natural microplankton assemblageswas 3%.     

Zooplankton feeding ecology: clearance and ingestion rates of the salps Thalia democratica, Cyclosalpa affinis and Salpa cylindrica on naturally occurring particles in the Mid-Atlantic Bight

Aggregate stages of the salps Thalia democratica, Cyclosalpaaffinis and Salpa cylindrica collected by SCUBA diving in theMid-Atlantic Bight were fed with naturally occurring food assemblages.This is one of the few studies where salps have been fed withnatural food assemblages. The estimated clearance rate for allspecies based on disappearance of chlorophyll varied from 82to 444 mL individual^–1 day^–1. Cell counts showedthat T. democratica mostly ingested carbon from autotrophicnanoflagellates and autotrophic dinoflagellates. Ingestion byS. cylindrica was primarily on larger prey, such as dinoflagellates,while C. affinis ingested auto- and heterotrophic nanoflagellates.All main prey types ingested by salps corresponded to thosethat contributed most to biomass at each experimental station.Thus, salps fed on naturally occurring particles primarily inproportion to prey biomass and to their mechanical capacityto be retained and ingested. Feeding by salps on dinoflagellatesand ciliates implies that they may act not only as potentialcompetitors with microzooplankton, but also as consumers ofthem.     

Plankton composition and cycling of carbon during the rainy season in a tropical coastal ecosystem, Zanzibar, Tanzania

Biomass, species composition and production of the planktoniccommunity were investigated during the rainy season in May andJune 1999 outside Zanzibar Island, Tanzania. In general, theplankton biomass of different organisms was uniform betweendepths as well as over time. The integrated water column primaryproduction ranged from 204 to 4142 mg C m^–2 day^–1.Bacterial production varied between 10 and 72 mg C m^–2day^–1, comprising ~5% of the total bacterial standingstock. The data obtained from these experiments are summarizedin a carbon budget. At the most 77% of the total primary productionchannelled through the heterotrophic flagellates, ciliates andheterotrophic dinoflagellates to higher trophic levels. Of theestimated carbon demand for mesozooplankton, 28% could potentiallybe met by ciliates and heterotrophic dinoflagellates.     

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

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