Pelagic carbon metabolism in a eutrophic lake during a clear-water phase

Dissolved and paniculate organic carbon (DOC and POC, respectively),primary production, bacterial production, bacterial carbon demandand community grazing were measured for 9 weeks in eutrophicFrederiksborg Slotssø. The period covered the declineof the spring bloom, a clear-water phase and a summer phasewith increasing phytoplankton biomass. The process rates andchanges in pools of organic carbon were combined in a carbonbudget for the epilimnion. The POC budget showed a close balancefor both the post-spring bloom and the clear-water phase, whilea surplus was found in the summer phase. Production of POC wasdominated by phytoplankton (2/3) compared to bacteria (1/3)during all phases, and there was a significant correlation betweenphytoplankton and bacterial production rates (r² = 0.48, P <0.039). Bacterial demand for DOC was balanced by productionand changes in the pool of DOC during the decline of the springbloom, but the calculated demand exceeded the supply by 81 and167%, respectively, during the other two periods. The discrepancywas most probably due to an underestimation of bacterial growthefficiency and an overestimation of in situ bacterial productionin carbon units. Production of bacterial substrate by zooplanktonactivity was estimated to be higher than the direct excretionof organic carbon from phytoplankton. The biological successionwas regulated by the balance between area primary productionand community grazing. The clear-water phase was initiated bya combination of low primary production due to low surface irradianceand high community grazing (100 mmol C m^–2 day^–1),which caused a decrease in phytoplankton biomass. However, dueto the high initial phytoplankton biomass, community grazingwas not high enough to cause a significant decrease in areaprimary production. The summer phase was initiated by a decreasein community grazing followed by an increase in phytoplanktonbiomass. Based on these observations and calculations of areaprimary production as a function of chlorophyll concentrations,we suggest that the possibility for zooplankton to regulatephytoplankton biomass in temperate lakes decreases with increasingnutrient level.     

Photosynthetic algal production, accumulation and release of phytoplankton storage carbohydrates and bacterial production in a gradient in daily nutrient supply

In a mesocosm experiment providing a gradient of semi-continuousaddition of mineral nutrient, production rates and mortalityof phytoplankton were estimated. Heterotrophic bacterial biomassand production rates and their responses to the mineral nutrientsadditions were also estimated. The purpose of the experimentwas to establish responses of the major biological factors asa function of nutrient amendments. Initial primary productionwas 0.47 µg C L^–1 day^–1. In the most fertilizedmesocosm, phytoplankton biomass increased at a specific rateof 0.4 day^–1 during the first week of the experiment,and on day 9 primary production reached a peak at 1027 µgC L^–1 day^–1. The responses in the other fertilizedmesocosms were intermediate, and in an unfertilized controlthe variables measured stayed almost constant throughout theexperiment. The termination of the blooms in the fertilizedmesocosms was a consequence of nitrogen limitation, and nitrogenlimitation subsequently induced storage of intracellular organicmaterial in the phytoplankton. In the mesocosm receiving thehighest daily dose of nutrients, strong post-bloom nutrientlimitation resulted in high phytoplankton mortality, and releaseof organic material from the algae supported the gradient’shighest heterotrophic bacterial production.     

Regulation of bacterial secondary production in two eutrophic lakes and in experimental enclosures

Bacterial cell number and secondary production of bacterioplanktonwere measured during two periods of 14 and 19 days, respectively,in experimental enclosures of lake water (each containing about5–7 m³ and in two Danish, eutrophic lakes. Additions ofphosphate and planktivorous fish to some of the enclosures inducedrapid changes in the phytoplankton biomass, primary productionand release of extracellular organic carbon (EOC). In some ofthe enclosures containing fish, release of EOC from phytoplanktoncon stituted from 36 to 55% of the bacterial secondary productiondetermined by means of [³H]thymidine incorporation into DNA.In others, such a relationship was not found, suggesting thatphytoplankton species-specific release rates of compositionof EOC might play a role in the microbial response. In enclosureswithout fish, released dissolved organic carbon from zooplanktongrazing activities could Sustain     

Population dynamics of bacterioplankton in an oligotrophic lake

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

Contribution of heterotrophic plankton to nitrogen regeneration in the upwelling ecosystem of A Coruna (NW Spain)

The contribution of heterotrophic plankton to nitrogen (N) regenerationin the water column, and its significance for the requirementsof phytoplankton, were studied at the seasonal scale in thecoastal upwelling ecosystem of A Coruña (Galicia, NWSpain). During 1995–1997, monthly measurements were takenof hydrographic conditions, dissolved nutrients, and abundanceand biomass of microplanktonic heterotrophs (bacteria, flagellatesand ciliates), phytoplankton and mesozooplankton (>200 µm).Additionally, series of experiments were conducted to quantifyN fluxes, including primary production (¹⁴C method), phytoplanktonuptake of nitrate, ammonium and urea (¹⁵N-labelling techniques),microheterotrophic regeneration of ammonium, mesozooplanktongrazing (chlorophyll gut-content method) and excretion of ammoniumby mesozooplankton. Two N budgets were built for the averagesituations of high (>100 mg C m^-2 h^-1) and low (<100 mgC m^-2 h^-1) primary production. The results revealed that phytoplanktonrelied strongly on regenerated ammonium all year round (33 and43% of total N uptake in high and low production situations,respectively). This demand for ammonium was closely matchedby regeneration rates of microplankton (0.14–0.25 mmolN m^-2 h^-1), whereas zooplankton contributed on average <10%to N regeneration. Likewise, zooplankton grazing had littledirect control on phytoplanktonic biomass. The results obtainedindicate that in the A Coruña upwelling system, N biomassof heterotrophic plankton is generally higher than phytoplanktonN biomass. The high rates of N regeneration measured also suggestthat a large proportion of the organic matter produced afteran upwelling pulse is recycled in the water column through themicrobial food web.     

Assessment of particulate organic matter in river water

Particulate organic matter in a downriver riffle of the Grand River, the largest Canadian Great Lakes tributary, was studied between June 1970 and April 1972. In winter and spring, concentrations of particulate organic matter (1.0–26.2 mg/l) varied with river flow. High summer levels (3.4–12.7 mg/l) were attributable to high autochthonous primary production. Mean chlorophyll a concentration in summer (29.8 mg/m³) was nearly 15 times higher than in winter, and 8 times the spring mean level. High algal cell counts (15,000–19,000 cells/l) also occurred in summer. Autochthonous and allochthonous contributions to the total particulate organic carbon input to the river in summer were estimated by daily organic input and river flow relationships, carbon to chlorophyll a and to pheopigments ratios. The allochthonous source accounted for 21.5% of the total organic carbon while the autochthonous contributed the remaining 78.5%. The latter included living algae (23.0%), senescent plant material (30.3%) and detritus (25.2% — including microbes). The study establishes a new approach whereby the various components of particulate organic matter in river water can be indirectly partitioned and their biomass estimated by using quantitative relationships among readily obtainable parameters of river flow, standing biomass, chlorophyll a and pheopigments.     

Bacterioplankton and Organic Carbon Dynamics in the Lower Mesohaline Chesapeake Bay

The mesohaline portion of the Chesapeake Bay is subject to annual summertime hypoxia and anoxia in waters beneath the pycnocline. This dissolved oxygen deficit is directly related to salinity-based stratification of the water column in combination with high levels of autochthonously produced organic matter and a very high abundance of metabolically active bacteria. Throughout the water column in the lower, mesohaline part of the bay, between the Potomac and Rappahannock rivers, near the southern limit of the mainstem anoxia, bacterial abundance often exceeded 10 × 10⁶ cells per ml and bacterial production exceeded 7 × 10⁹ cells per liter per day during summer. Bacterial biomass averaged 34% (range, 16 to 126%) of the phytoplankton biomass in summer. These values are equal to or greater than those found farther north in the bay, where the oxygen deficit is more severe. Seasonal variations in bacterial abundance and production were correlated with phytoplankton biomass (lag time, 7 to 14 days), particulate organic carbon and nitrogen, and particulate biochemical oxygen demand in spring; but during summer, they were significantly correlated only with dissolved biochemical oxygen demand. During summer, dissolved biochemical oxygen demand can account for 50 to 60% of the total biochemical oxygen demand throughout the water column and 80% in the bottom waters. There is a clear spring-summer seasonal shift in the production of organic matter and in the coupling of bacteria and autochthonous organic matter. The measurement of dissolved, microbially labile organic matter concentrations is crucial in understanding the trophic dynamics of the lower mesohaline part of the bay. The absolute levels of organic matter in the water column and the bacterial-organic carbon relationships suggest that a lower bay source of organic matter fuels the upper mesohaline bay oxygen deficits.     

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

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

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.     

Response of plankton to nutrients,planktivory and terrestrial organic matter: a model analysis of whole‐lake experiments

Terrestrial organic matter can be assimilated by aquatic consumers but implications for biomass and production are unresolved. An ecosystem model was fit to estimate effects of phosphorus (P) load, planktivory, and supply rate of terrestrial particulate organic carbon (TPOC) on phytoplankton and zooplankton in five whole‐lake experiments. Phytoplankton biomass increased with P load and planktivory and decreased with TPOC supply rate. Zooplankton biomass increased with P load and responded weakly to planktivory and TPOC supply rate. Zooplankton allochthony (proportion of carbon from terrestrial sources) decreased with P load and planktivory and increased with TPOC supply rate. Lakes with low allochthony (< 0.3) had wide ranges of phytoplankton and zooplankton biomass and production, depending on P load and planktivory. Lakes with high allochthony (> 0.3) had low biomass and production of both phytoplankton and zooplankton. In summary, terrestrial OC inhibits primary production and is a relatively low‐quality food source for zooplankton.     

Primary and bacterial production in lakes: are they coupled over depth?

The coupling of primary and bacterial production over depthwas examined in three lakes which differed greatly in verticalpatterns of primary productivity. We measured bacterial production,chlorophyll and light, and estimated primary production in PaulLake (Gogebic County, Michigan) and Crystal and Trout lakes(Vilas County, Wisconsin) during the summer stratification period(May–September 1991). Bacterial productivity was measuredusing the [³H]leucine incorporation method and primary productivityestimated from measured photosynthesis–irradiance relationships.Three distinct vertical patterns were observed. In Paul Lake,bacterial production was highest at the interface between theaerobic and anaerobic layers, well below the depth of maximumprimary production. In Crystal Lake, bacterial production wasuniform with depth, although primary productivity was highestin the hypolimnion. In the largest lake. Trout Lake, primaryand bacterial production tended to co-vary with maximum ratesof both processes occurring in the metalimnion. Overall, bacterialproductivity was poorly related to contemporaneous primary productionin the three lakes, suggesting that other factors, such as nutrientrecycling, phytoplankton loss rates and allocthonous loading,determine patterns in the depth distribution of bacterial productivity.     

Species-specific phytoplankton sedimentation in relation to primary production along an inshore--offshore gradient in the Baltic Sea

The temporal and spatial variability in the quality and quantityof settling phytoplankton material in relation to concurrentprimary production was studied using sediment traps at threecoastal stations from a semi-enclosed bay (Pojo Bay) throughthe outer archipelago to the open Gulf of Finland. The fluxof settling phytoplankton was high (9.3 g C m^–2period^–1)in Pojo Bay, especially in spring, and lower in the archipelago(8.1 g C m^–2 period^–1) and open-sea area (5.2 gC m"2 period"1), although the primary production followed theopposite pattern. A large influx of allochthonous material intoPojo Bay in spring brought allochthonous phytoplankton cellsinto the traps, but limited primary production. Diatoms werethe most abundant settled phytoplankton at all stations, butthe species composition varied between Pojo Bay (Aulacoseiraspp., Rhizosolenia minima) and the outer stations (Skeletonemacostatum, Chaetoceros spp.)At the outer stations, migratingdinoflagellates (Peridiniella catenate) comprised part of thesettling material in spring. The high settling flux of the cyanophyteAphanizomenon flos-aquae is discussed. The species compositionof the phytoplankton assemblage influenced the proportion ofthe total organic carbon sedimentation that consisted of phytoplanktoncarbon.     

Bacterial Activity in a Reservoir Determined by Autoradiography and its Relationships to Phyto- and Zooplankton

In the drinking water reservoir Římov (Southern Bohemia) bacterioplankton was studied during 1983. Special attention was given to the relationships between parameters of bacterial abundance, total and individual activity. Bacterial counts and biomass was assessed and autoradiographic determinations of the proportion of active bacteria incorporating thymidine (Th) and mixture of amino acids (AA) and total uptake rate of AA were made over a year in the surface layer and during summer stratification from the thermocline and 15 m depth. Specific activity of metabolically active bacteria (SAMAB) and specific activity per unit of biomass (SAUB) were negatively correlated with counts of metabolizing cells and with bacterial biomass, respectively. Total and individual heterotrophic activity and counts of bacteria coincided with the changes of phytoplankton biomass, whereas bacteria incorporating Th were more tightly correlated with primary production. The most significant relation of metabolically active bacteria was found to cladoceran biomass. Thus, this part of heterotrophic bacterial activity seems to be stimulated by leakage of dissolved organic matter from phytoplankton being disrupted and incompletely digested by cladocerans rather than from healthy photosynthetizing cells.     

Short communication. Direct and indirect effects of strong grazing by Daphnia galeata on bacterial production in an enclosure experiment

Bacterial production was stimulated in Daphnia enclosures at the beginning of the experiment due to the release of dissolved organic carbon during Daphnia grazing of algae (sloppy feeding). In contrast, bacterial production decreased in the treatments at the end of the experiment. The decline was not caused by reduction of bacterial biomass, but by decreasing biomass-specific production due to a decline of the resources for bacterial growth (phytoplankton biomass and production).      

Regulation of Bacterioplankton Production and Cell Volume in a Eutrophic Estuary

During three periods of 16 to 25 days, bacterioplankton production, bacterial cell volume, chlorophyll a, CO₂ assimilation, and particulate organic carbon were measured in enclosures situated in the eutrophic estuary Roskilde Fjord, Denmark. The enclosures were manipulated with respect to sediment contact and contents of inorganic nutrients, planktivorous fish, and suspension-feeding bivalves. Nutrient enrichment, the presence of suspension feeders, and sediment contact induced pronounced changes in bacterial production, as well as minor changes in bacterial cell volume; however, these effects seemed to be indirect, transmitted via phytoplankton. Bacterial production, measured as [³H]thymidine incorporation, closely followed changes in phytoplankton biomass and production, with time lags of 5 to 10 days. Good correlations of mean bacterioplankton production to chlorophyll a concentration and CO₂ assimilation suggested phytoplankton to be the dominating source of bacterial substrate, apparently independent of nutrient stress. Zooplankton >140 μm, bivalves, and sediment seemed to provide insignificant, if any, substrate for bacterioplankton, and benthic suspension feeders seemed not to act as direct competitors for dissolved organic carbon. The bacterioplankton mean cell volume, measured by image analysis, changed seasonally, with the smallest cells during the summer. Within each period, the bacterial cell volume correlated positively to growth rate and negatively to temperature.     

Limitation of Bacterial Growth by Dissolved Organic Matter and Iron in the Southern Ocean

The importance of resource limitation in controlling bacterial growth in the high-nutrient, low-chlorophyll (HNLC) region of the Southern Ocean was experimentally determined during February and March 1998. Organic- and inorganic-nutrient enrichment experiments were performed between 42°S and 55°S along 141°E. Bacterial abundance, mean cell volume, and [³H]thymidine and [³H]leucine incorporation were measured during 4- to 5-day incubations. Bacterial biomass, production, and rates of growth all responded to organic enrichments in three of the four experiments. These results indicate that bacterial growth was constrained primarily by the availability of dissolved organic matter. Bacterial growth in the subtropical front, subantarctic zone, and subantarctic front responded most favorably to additions of dissolved free amino acids or glucose plus ammonium. Bacterial growth in these regions may be limited by input of both organic matter and reduced nitrogen. Unlike similar experimental results in other HNLC regions (subarctic and equatorial Pacific), growth stimulation of bacteria in the Southern Ocean resulted in significant biomass accumulation, apparently by stimulating bacterial growth in excess of removal processes. Bacterial growth was relatively unchanged by additions of iron alone; however, additions of glucose plus iron resulted in substantial increases in rates of bacterial growth and biomass accumulation. These results imply that bacterial growth efficiency and nitrogen utilization may be partly constrained by iron availability in the HNLC Southern Ocean.     

Phytoplankton seasonal dynamics in a Mediterranean coastal lagoon: emphasis on the picoeukaryote community

The dynamics of the phytoplankton community were investigatedin a marine coastal lagoon (Thau, NW Mediterranean) from February1999 to January 2000. Dilution experiments, chlorophyll a (Chla) size-fractionation and primary production measurements wereconducted monthly. Maximum growth and microzooplankton grazingrates were estimated from Chl a biomass fractions to separatepico- from nano- and microphytoplankton and by flow cytometryto distinguish between picoeukaryotes and picocyanobacteria.In spring, the phytoplankton community was dominated by Chaetocerossp. and Skeletonema costatum, which represented most of biomass(B) and primary production (P). Nano- and microphytoplanktongrowth was controlled by nutrient availability and exceededlosses due to microzooplankton grazing (g). Picoeukaryote andcyanobacteria growth was positively correlated with water temperatureand/or irradiance, reaching maximum values in the summer (2.38and 1.44 day^–1 for picoeukaryotes and cyanobacteria, respectively).Picophytoplankton accounted for 57% of the biomass-specificprimary productivity (P/B). Picophytoplankton was strongly controlledby protist grazers (g = 0.09–1.66 day^–1 for picoeukaryotes,g = 0.25–1.17 day^–1 for cyanobacteria), and microzooplanktonconsumption removed 71% of the daily picoplanktonic growth.Picoeukaryotes, which numerically dominate the picoplanktoncommunity, are an important source of organic carbon for theprotistan community and contribute to the carbon flow to highertrophic levels.     

Phytoplankton, bacterial production and protozoan bacterivory in stratified, brackish-water Lake Shira (Khakasia, Siberia)

Rates of oxygenic and anoxygenic photosynthesis, chemoautotrophic and heterotrophic bacterial production and protozoan bacterivory were measured in the pelagic zone of the stratified brackish-water lake with the purpose to determine the vertical distribution of these processes and to estimate their significance in the functioning of planktonic community of the lake. In midsummer, total daily primary productivity was about 1.3 g C m^–2, of which 72% was produced by the phytoplankton, 24% by the chemoautotrophic bacteria, and only 4% by the phototrophic sulphur bacteria. Thus anoxygenic photosynthesis is a negligible source of organic matter in the lake. The production of heterotrophic bacteria averaged 1.5 g C m^–2 d^–1 and exceeded the total photosynthesis of phytoplankton and photosynthetic bacteria by a factor of 1.5. The estimated total primary production was too low to sustain the bacterial production. Probably the carbon cycle in the lake is dependent on the input of allochthonous organic matter. As a rule, the maximal rates of primary production and heterotrophic bacterial production were found in the chemocline or at the upper boundary of the chemocline. Heterotrophic flagellates dominated among the protozoan populations and were the major consumers of the bacterioplankton production in the lake. They showed maximal ingestion rates from 2.3 to 2.9 mg C m^–3 h^–1 at the upper boundary of the chemocline, where they consumed from 50 to 54% of the production of heterotrophic bacteria. Data obtained indicate that in Lake Shira the oxic-anoxic interface is the site of the most intensive production and mineralization of organic matter.     

Factors regulating autotrophy and heterotrophy in the main channel and an embayment of a large river impoundment

We characterized seasonal patterns of phytoplankton and bacterial biomass, production and nutrient limitation along a lateral transect within a large river impoundment. We hypothesized that the balance between autotrophy and heterotrophy was related to depth gradients and differences in water residence time (WRT) between the main channel and an embayment. Heterotrophy predominated in the main channel with bacterial production exceeding phytoplankton production by a factor of 3.3. In the embayment, autotrophy and heterotrophy were more closely balanced (ratios of bacterial to phytoplankton production ca. 0.8). Phytoplankton and bacterial biomass were positively correlated with WRT. However, WRT accounted for less than 50% of variation and its predictive power was comparable to models based on nutrient or DOC concentrations. Bacterial production was correlated with phytoplankton biomass and production suggesting that algal-derived C may be an important substrate for bacterial growth even in systems dominated by allochthonous inputs. Our experimental data suggest that nutrient limitation may be important particularly in embayments where biomass was somewhat higher and substrate concentrations were lower. Nutrient limitation in the main channel was rare whereas N and P amendments consistently stimulated phytoplankton growth rates in the embayment. Bacterial cell densities did not respond to nitrogen or phosphorus additions in either the main channel or embayment.     

Factors controlling production of phytoplankton and bacteria under ice in a humic, boreal lake

The factors controlling pelagic primary and bacterial productionof a humic, boreal lake in winter were investigated, combininglaboratory and field experiments where some of the predictedconsequences of the climate change, i.e.the increased load ofphosphate-phosphorus and dissolved organic matter (DOM), weresimulated. In situ incubations were performed in eight acrylictubes lowered underneath the ice cover for 1–4 months.In the lake, production of phytoplankton (0.03–0.33 µgC l^–1 day^–1) was lower than that of bacteria (0.2–2.3µg C l^–1 day^–1) from the end of January tomid-April. Later in spring, the light conditions improved dueto the disappearance of snow and finally ice itself, and primaryproduction was revived. The importance of light as the factorcontrolling primary production in winter was confirmed in laboratoryexperiments where additions of phosphorus and DOM did not enhancethe primary production. These same enrichments resulted in highergrowth rates and production of bacteria. However, bacterioplanktonwas simultaneously controlled by heterotrophic flagellates,as in the laboratory experiments the exclusion of flagellatesalways resulted in higher yields of bacteria of increased cellsize. There was also some evidence that the quality of substratesis of importance for microbial activities. The importance oftemperature was highlighted with the significant correlation(r² = 0.59) between bacterial production and temperature withinthe range 0.6–2.1C. Thus, on the boreal zone the possiblewarming of climate may lead to enhanced activities in winter,but under unchanged light conditions no effects on primary productionwill be expected.