Picoplankton in Six New Zealand Lakes: Abundance in Relation to Season and Trophic State

The abundance of picoplankton (0.2-2 μm) was measured seasonally in the surface waters of six New Zealand lakes that represent a range of trophic states. The lakes were: Wakatipu, Te Anau, Manapouri, Hayes, Mahinerangi and Ross Creek Reservoir. Among the lakes, picoplankton abundance was associated positively with temperature; picoplankton were most abundant in summer and autumn when they attained densities of 108,000-270,000 cells/ml in the oligotrophic lakes. In these lakes, prokaryotic picoplankton was generally an order of magnitude more abundant than eukaryotic picoplankton. Consistent with the hypothesis that picoplankton are more important in oligotrophic than eutrophic ecosystems, there was a weak negative correlation between the density of prokaryotic picoplankton in the lakes and the level of chlorophyll a. The presence of large numbers of chroococcoid cyanobacteria in the guts of Ceriodaphnia dubia and Bosmina meridionalis implies that prokaryotic picoplankton are collected, but not digested, by these species.     

Phototrophic Picoplankton in Temperate Lakes: Seasonal Abundance and Importance along a Trophic Gradient

The seasonal development of autotrophic picoplankton was investigated in seven Danish lakes representing a eutrophication gradient. Highest cell abundance between 1.5 to 6 × 10⁵ cells ml⁻¹ were found in mid-summer. Minor peaks were observed in spring. In winter, densities were below 10³ ml⁻¹. The highest relative picoplankton contribution to total autotrophic biomass also occurred in mid-summer. In the eutrophic lakes and one humic lake the average seasonal contribution of picoplankton to total chlorophyll was below 1% increasing to 5-8% in the meso- and oligotrophic clear water lakes. During short periods the proportion of picoplankton did reach 25%. The higher relative importance of picoplankton in less productive lakes was not due to higher actual chlorophyll concentrations, but due to a much more pronounced response by larger algae at higher nutrient loading. Both cyanobacteria and eukaryote organisms were present as picoplankton. Only eukaryotes were found in one eutrophic lake and an acidic, humic lake. In the eutrophic lakes eukaryote picoplankton was dominant; both with respect to cell densities and biovolume, whereas cyanobacteria dominated the two meso-oligotrophic lakes. Autotrophic picoplankton were present in all lake types, however their importance seemed to be less in most eutrophic lakes than in less productive, meso-oligotrophic lakes.     

The impact of substrate and lake trophy on the biomass and nutrient status of benthic algae

Algal biomass, C:N:P (carbon:nitrogen:phosphorus) ratios and APA (biomass specific alkaline phosphatase activity) were measured in benthic algal communities on living substrates (mussels and macrophytes) and on rocks and stones (epilithon) in three lakes of different trophy. Benthic algal communities on living substrates had lower C:N:P ratios than epilithon, whereas algal biomass was highest on rocks and stones. Benthic algal biomass increased with the trophic level of a lake despite an increase of C:N:P ratios in the benthic community. The differences in C:N:P ratios and algal biomass between lakes of different trophy were higher on inert substrates than on macrophytes and mussels, probably because algae on living substrates could compensate a poor nutrient supply from lake water with substrate nutrients. However, the substrate was not, as expected, the most important nutrient supply in the oligotrophic lake, but in the eutrophic lake. Therefore, differences between inert and living substrates in a single lake were highest in the eutrophic lake. APA values of the oligotrophic lake were very high especially for benthic algae on stones, indicating an ability of the community to take up nutrients from organic sources. In conclusion, living substrates were an important nutrient source for benthic algae and the importance of this nutrient supply did not decrease with increasing lake trophy.     

Seasonal Changes in Chlorophyll-containing Picoplankton Populations of Ten Lakes in Northern England

Key features of photosynthetic picoplankton populations were compared during 1988 in ten lakes in northern England ranging from oligotrophic to slightly eutrophic; two of the three eutrophic lakes were shallow and lacked a thermocline. Measurements were made at 0.5 m depth of temperature, total chlorophyll a, chlorophyll-containing picoplankton cell density, mean picoplankton cell volume and percentage of phycoerythrin-rich cells in the total picoplankton population. All lakes showed maxima for total chlorophyll concentration and picoplankton cell density in mid- to late summer. The maximum value for picoplankton density ranged from 3.4 × 10³ (Esthwaite Water) to 1.3 × 10⁶ cells ml⁻¹ (Ennerdale Water). There was a significant negative relationship (p < 0.05) between log₁₀ of maximum picoplankton cell density and maximum total chlorophyll, the latter being taken as an indicator of lake trophic status. The ratio of maximum to minimum picoplankton density during the year in a particular lake ranged from 39 to 2360 and showed no obvious relationship to lake type. Overall, the seasonal range in picoplankton density was about one order of magnitude greater than the range in total chlorophyll a, but there were considerable differences between lakes. Phycoerythrin-rich picoplankton as a percentage of total picoplankton reached a maximum in summer in all lakes. Values were always very low (<5%) in the two shallow eutrophic lakes, but reached 97% and over in the four most oligotrophic lakes. In two of the oligotrophic lakes, Wast-water and Ennerdale Water, phycoerythrin-rich picoplankton was a major component of the summer phytoplankton biomass.     

Abundance and distribution of picoplankton in tropical, oligotrophic Lake Kivu, eastern Africa

1. We used flow cytometry to characterize freshwater photosynthetic picoplankton (PPP) and heterotrophic bacteria (HB) in Lake Kivu, one of the East‐African great lakes. Throughout three cruises run in different seasons, covering the four major basins, phycoerythrin‐rich cells dominated the PPP. Heterotrophic bacteria and PPP cell numbers were always high and spatial variations were modest. This represents an important difference from temperate and high latitude lakes that show high fluctuations in cell abundance over an annual cycle. 2. Three populations of picocyanobacteria were identified: one corresponded to single‐cells (identified as Synechococcus by epifluorescence microscopy, molecular methods and pigment content), and the two other that most probably correspond to two and four celled colonies of the same taxon. The proportion of these two subpopulations was greater under stratified conditions, with stronger nutrient limitation. 3. High PPP concentrations (c. 10⁵ cell mL^?1) relative to HB (c. 10⁶ cell mL^?1) were always found. Lake Kivu supports relatively less bacteria than phytoplankton biomass than temperate systems, probably as a consequence of factors such as temperature, oligotrophy, nutrient limitation and trophic structure. 4. A review of PPP concentration across aquatic systems suggests that the abundance of Synechococcus‐like cyanobacteria in large, oligotrophic, tropical lakes is very high. 5. Photosynthetic picoplankton cell abundances in the oligotrophic tropical lakes Kivu and Tanganyika are comparable to those of eutrophic temperate lakes. This apparently contradicts the view that PPP abundance increases with increasing eutrophy. More data on PPP in tropical lakes are needed to explore further this particular pattern.     

The Seasonal Dynamics and Composition of Photosynthetic Picoplankton Communities in Temperate Lakes in Ontario,Canada

The seasonal abundance and composition of photosynthetic picoplankton (0.2-2 μm) was compared among five oligotrophic to mesotrophic lakes in Ontario. Epilimnetic picocyanobacteria abundance followed a similar pattern in all lakes; maximum abundance (2-4 × 10⁵ cells · ml⁻¹) occurred in late summer following a period of rapid, often exponential increase after epilimnetic temperatures reached 20 °C. In half of the lakes picocyanobacteria abundance was significantly correlated with temperature, while in other lakes the presence of a small spring peak resulted in a poor correlation with temperature. In all lakes there was a significant correlation between epilimnetic abundance and day of the year. Correlations with water chemistry parameters (soluble reactive phosphorus, total phosphorus, particulate C: P and C: N) were generally weaker or insignificant. However, in the three lakes with the highest spring nitrate concentrations, a significant negative correlation with nitrate was observed. During summer stratification, picocyanobacteria abundance reached a maximum within the metalimnion and at or above the euphotic zone (1% of incident light) in all lakes. These peaks were not related to nutrient gradients. The average total phytoplankton biomass ranged from 0.5 g m⁻³ (wet weight) in the most oligotrophic lake to 1.4 g m⁻³ for the most mesotrophic with picoplankton biomass ranging from 0.01 g m⁻³ to 0.3 g m⁻³. Picocyanobacteria biomass comprised 1 to 9 % of total phytoplankton biomass in late summer, but in one year for one lake represented a maximum of 56%. Other photosynthetic picoplankton (unidentified eukaryotes, Chlorella spp. Nannochloris spp.), although less abundant (10³ cells · ml⁻¹) than picocyanobacteria, represented biomass equal or greater than that of the picocyanobacteria in spring and early summer. On average, half of the photosynthetic picoplankton biomass was eukaryotic in the more coloured lakes, while in the clear lakes less than 20% was eukaryotic. Among the lakes there was a significant positive correlation between the average light extinction coefficient and the proportion of eukaryotic biomass of the picoplankton. In mesotrophic Jack's Lake, the contribution of picoplankton to the maximum photosynthetic rate ranged from 10 to 47% with the highest values in the spring (47%) and late summer (33%), as a result of eukaryotic picoplankton and picocyanobacteria respectively. Picocyanobacteria cell specific growth rates were high during July (0.6-0.8 day⁻¹) and losses were close to 80% of the growth rate. Thus, despite low biomass, photosynthetic picoplankton populations appeared to turn over rapidly and potentially contributed significantly to planktonic food webs in early spring and late summer.     

Effect of macrophyte community composition and nutrient enrichment on plant biomass and algal blooms

Submerged freshwater macrophytes decline with increasing eutrophication. This has consequences for ecosystem processes in shallow lakes and ponds as macrophytes can reduce algal blooms under eutrophic conditions. We hypothesize that the productivity of submerged vegetation, biomass change under eutrophication and the suppression of algal blooms may be affected by macrophyte community composition. To test our hypothesis, we established three macrophyte community types in 36 fishless experimental ponds: one dominated by the oligotrophic species Chara globularis, one dominated by the eutrophic species Potamogeton pectinatus and a diverse vegetation which became co-dominated by Elodea nuttallii and C. globularis, and we fertilized half of the ponds.The macrophyte communities produced different amounts of biomass and they responded differently to fertilization. The community dominated by Potamogeton produced the lowest overall biomass, but was not affected by nutrient addition. The communities dominated by Chara and co-dominated by Elodea and Chara produced more than four-fold the amount of biomass produced in Potamogeton communities under oligotrophic conditions, but were strongly negatively affected by nutrient addition.Phytoplankton abundance did not differ significantly among the plant community types, but showed large variation within community types. There was a significant negative relationship between spring macrophyte biomass and the probability of summer algal blooms. The occurrence of algal blooms coincided with low daphnid densities and high pH (>10).We conclude that the macrophyte community composition, characterized by the dominant species, strongly affected the amount of biomass production as well as the short-term response of the vegetation to nutrient enrichment. Macrophyte community composition had no direct effect on algal blooms, but can affect the occurrence of algal blooms indirectly as these occurred only in ponds with low (<100 g/m² DW) spring macrophyte biomass.     

Predominance of picoplankton and nanoplankton in eutrophic Calder Lake

A study was conducted to examine factors regulating the biomass of algal picoplankton in Calder Lake, a small eutrophic lake in southern New York state. A particular focus was a current paradigm which suggests that larger cells may dominate in nutrient-rich waters, while smaller cells may predominate only in oligotrophic waters. Over two years, phytoplankton biomass consisted predominantly (74% on average) of very small organisms; nanoplankton (<20 to 2 µm: 39%) and picoplankton (<2 µm to 0.2 µm: 35%), despite the presence of surface blooms of colonial cyanobacteria (Microcystis aeruginosa, Anabaena limnetica), and dense metalimnetic populations of the dinoflagellate Ceratium hirundinella. This dimictic system is characterized by relatively high levels of total P (max = 85, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiEayaara% aaaa!3702!\[\bar x\] = 9.7 µg P/L), inorganic P (max = 26, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiEayaara% aaaa!3702!\[\bar x\] = 4.5 µg P/L), and total inorganic N (max = 285, % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGqiVu0Je9sqqrpepC0xbbL8F4rqqrFfpeea0xe9Lq-Jc9% vqaqpepm0xbba9pwe9Q8fs0-yqaqpepae9pg0FirpepeKkFr0xfr-x% fr-xb9adbaqaaeGaciGaaiaabeqaamaabaabaaGcbaGabmiEayaara% aaaa!3702!\[\bar x\] = 85 µg P/L), but larger forms were rarely the most abundant. Unlike some marine systems, greater abundance of algal picoplankton was not associated with deeper strata (low light), or warmer temperatures. Data suggest that midsummer nutrient limitation, especially P-limitation, favors the development of pico- and nanoplankton in the limnetic zone of eutrophic lakes.     

Summer fluctuations of microbial planktonic communities in a eutrophic lake--Cierva Point, Antarctica

A eutrophic lake at Cierva Point, Antarctic Peninsula was surveyedduring the summers of 1997 and 1998. Phytoplankton size fractions(micro-, nano- and picoplankton) were analysed, as well as theabundance of bacterioplankton and planktonic ciliates. No permanentvertical stratification was found owing to the shallowness ofthe lake. Both nutrient concentrations and chlorophyll a valuesindicated highly eutrophic conditions, which are a consequenceof a natural enrichment by seabirds. Significant differencesin temperature between the 1997 and 1998 seasons strongly influencedmost of the biological features. The phytoplankton communityshowed a high algal species-richness, with important contributionsof epilithic, cryobiontic and soil algae. The dominant algalgroup was Chlorophyta, mainly represented by Chlamydomonas aff.celerrima, followed by Chl. aff. braunii. Some replacement ofphytoplanktonic species took place in summer and was more evidentin 1998. Picophytoplankton reached high densities, similar tothose reported from other Antarctic lakes. Bacterioplanktonabundances were typical of eutrophic and hypereutrophic lakes.There was a positive correlation between bacterial and totalphytoplankton abundance. Ciliates reached some very high peaks,with higher figures than those reported for other Antarcticsystems with similar trophic status.     

Carbon-14 Uptake by Picoplankton and Total Phytoplankton in Eight New Zealand Lakes

Eight New Zealand lakes were surveyed for ¹⁴C uptake by phytoplankton as a function of light intensity. The results support the view that the photosynthetic picoplankton is an important contributor to primary productivity in oligotrophic lakes but is relatively unimportant in more eutrophic lakes. A comparison of carbon uptake vs. light intensity characteristics (P vs. I) of the picoplankton size class vs. that of the total phytoplankton community supports the view that the picoplankton size class may be adapted to utilization of dimmer light.     

Relations between trophic state indicators and plant biomass in Florida lakes

We collected quantitative data on macrophyte abundance and water quality in 319 mostly shallow, polymictic, Florida lakes to look for relationships between trophic state indicators and the biomasses of plankton algae, periphyton, and macrophytes. The lakes ranged from oligotrophic to hypereutrophic with total algal chlorophylls ranging from 1 to 241 mg m^–3. There were strong positive correlations between planktonic chlorophylls and total phosphorus and total nitrogen, but there were weak inverse relationships between the densities of periphyton and the trophic state indicators total phosphorus, total nitrogen and algal chlorophyll and a positive relationship with Secchi depth. There was no predictable relationship between the abundance of emergent, floating-leaved, and submersed aquatic vegetation and the trophic state indicators. It was only at the highest levels of nutrient concentrations that submersed macrophytes were predictably absent and the lakes were algal dominated. Below these levels, macrophyte abundance could be high or low. The phosphorus–chlorophyll and phosphorus–Secchi depth relationships were not influenced by the amounts of aquatic vegetation present indicating that the role of macrophytes in clearing lakes may be primarily to reduce nutrient concentrations for a given level of loading. Rather than nutrient concentrations controlling macrophyte abundance, it seems that macrophytes acted to modify nutrient concentrations.     

Modelling the effects on phytoplankton communities of changing mixed depth and background extinction coefficient on three contrasting lakes in the English Lake District

1. The process‐based phytoplankton community model, PROTECH, was used to model the response of algal biomass to a range of mixed layer depths and extinction coefficients for three contrasting lakes: Blelham Tarn (eutrophic), Bassenthwaite Lake (mesotrophic) and Ullswater (oligotrophic). 2. As expected, in most cases biomass and diversity decreased with decreasing light availability caused by increasing the mixed depth and background extinction coefficient. The communities were generally dominated by phytoplankton tolerant of low light. Further, more novel, factors were identified, however. 3. In Blelham Tarn in the second half of the year, biomass and diversity did not generally decline with deeper mixing and the community was dominated by nitrogen‐fixing phytoplankton because that nutrient was limiting to growth. 4. In Bassenthwaite Lake, changing mixed depth influenced the retention time so that, as the mixed depth declined, the flushing rate in the mixed layer increased to the point that only fast‐growing phytoplankton could dominate. 5. In the oligotrophic Ullswater, changing the mixed depth had a greater effect through nutrient supply rather than light availability. This effect was observed when the mixed layer was relatively shallow (<5.5 m) and the driver for this was that the inflowing nutrients were added to a smaller volume of water, thus increasing nutrient concentrations and algal growth. 6. Therefore, whilst changes in mixed depth generally affect the phytoplankton via commonly recognized factors (light availability, sedimentation rate), it also affected phytoplankton growth and community composition through other important factors such as retention time and nutrient supply.     

Effects of nitrogen,phosphorus and carbon enrichment on planktonic and periphytic algae in a softwater,oligotrophic lake in Florida,USA

The objective of this study was to investigate nutrient limitation of algal abundance in Anderson-Cue Lake, a softwater clear oligotrophic lake in north-central Florida. Nutrient diffusing clay pots and cylindrical enclosures were used in the field to test effects of different combinations of nitrogen, phosphorus, silica, and carbon on algal standing crop and composition of periphytic and planktonic algae, respectively. Effects of nutrient enrichment on periphytic algae were examined in two studies conducted 31 May – 8 July and 10 June – 15 July 1991. Nutrient effects on planktonic algae were examined in one study from 13 June – 1 July 1991. Planktonic and periphytic algal biovolume was significantly higher (p<0.05) when nitrogen and carbon were added in combination than with treatments without nitrogen, carbon, or nitrogen and carbon. Treatments with nitrogen and carbon combined resulted in lower algal diversity and dominance by coccoid green algae andScenedesmus. Results indicate that carbon and nitrogen can be limiting factors to algal growth in Anderson-Cue Lake and possibly other lakes of similar water quality.     

Distribution of planktonic ciliates in highly coloured subtropical lakes: comparison with clearwater ciliate communities and the contribution of myxotrophic taxa to total autotrophic biomass

SUMMARY 1. The planktonic ciliate communities of eleven organically coloured north and central Florida lakes representing a variety of trophic conditions were examined during 1979–80. The total abundance and biomass of ciliates were not significantly different from comparable clearwater lakes and only minor taxonomic replacements were noted at the order level.
2. Timing of population peaks of oligotrophic lakes was dissimilar to clearwater lakes of the same trophic state, but seasonality in meso-trophic and eutrophic lakes resembled patterns described for comparable clearwater lakes.
3. Various ciliate components were strongly correlated with chlorophyll a concentrations, but only moderately correlated to dominant phytoplankton groups. No significant correlations were found between ciliate components and bacterial abundance.
4. Myxotrophic taxa numerically dominated oligotrophic systems, particularly during midsummer, and accounted for a large percentage of the total ciliate biomass. Estimates of the ciliate contribution to total autotrophic biomass indicate that these zoochlorellae-bearing protozoa may account for much of the autotrophic biomass during midsummer periods in coloured lakes, and thus may lead to an overestimation of phytoplankton standing crops available to zooplankton grazers if chlorophyll a is used as a surrogate measure of algal biomass.     

Uncoupling of chlorophyll and nutrients in lakes – possible reasons,expected consequences

Total phosphorus and total nitrogen explained a low percentage of summer chlorophyll variability in epilimnia of the Great Masurian Lakes. Division of the whole data set into two subgroups of lakes improved approximation of the chlorophyll nutrient relationship but revealed also functional differences between the lakes distinguished in that way. Chlorophyll in eutrophic lakes correlated well with nitrogen and phosphorus, that in mesotrophic lakes (those with summer chlorophyll <=22 mg m^–3 as calculated in the model) was related to none of the nutrients. Higher summer chlorophyll content in epilimnetic waters was accompanied by higher chl:PP and chl:PN ratios. Algal adaptation to poor light conditions in eutrophic lakes is postulated as a possible reason for that difference.Chlorophyll – nutrient relationships varied with the trophic status of lakes. Epilimnetic chlorophyll strictly followed phosphorus changes in eutrophic lakes but did not do so in mesotrophic ones. Detailed comparison of selected meso- and eutrophic lakes showed marked differences in the seasonal changes of chlorophyll and nutrient concentrations and in sedimentation rates, especially in spring. Nutrient limitation rather than zooplankton grazing is suggested as a possible mechanism of controlling algal abundance and the sequence of spring events in a eutrophic lake. It is hypothesised that phosphorus turnover in eutrophic lakes is dominated by seasonal vertical fluxes, while in mesotrophic lakes it is more conservative with consumption and regeneration restricted mostly to metalimnion. Possible consequences of such conclusion are discussed in the paper.     

Phytoplankton structure in different lake types in central Finland

Phyloplankton structure and its relation to physical and chemical properties of the water was studied in 58 central Finnish lakes. The biomass ranged from 0.2 to 14.2 g m⁻³ and the number of taxa per sample ranged from 33 to 152. The lakes were grouped into 5 types according to their trophic state: eutrophic, dyseutrophic, mesotrophic, oligotrophic, and acid oligotrophic lakes. The average biomass in eutrophic lakes was 5.57 g m⁻³, in dyseutrophic 3.54 g m⁻³, 1.23 g m⁻³ in mesotrophic, 0.52 g m⁻³ in oligotrophic and 0.39 g ⁻³ in acid oligotrophic lakes. The average number of taxa per sample in the corresponding lake types were 109. 1, 79.3, 97.9, 90.9 and 43.8, respectively. The phytoplankton communities in eutrophic lakes were characterized by blue-green algae (21.2% of total biomass) and green algae (18.7% of total biomass). In dyseutrophic lakes the proportion of green algae was much smaller (7.2% of total biomass) than in eutrophic lakes, whereas the proportion of diatoms and cryptophytes was higher (28.2 and 20.4% of total biomass, respectively). Chrysophytes dominated in the oligotrophic and mesotrophic lakes (27.3–39.9% of total biomass). The contribution of dinoflagellates to the total biomass was highest in the most oligotrophic acidified lakes and in those lakes the relative proportions of blue-green and green algae were much higher than in the typical oligotrophic lakes. The lakes were also grouped into 8 community types according to the dominating algal group. Cyanophyceae- and Chlorophyceae-types characterized the eutrophic lakes, whereas Chrysophyceae-Dinopheceae-type was typical for most oligotrophic lakes. The other 5 types occurred in mesotrophic and oligotrophic lakes but the physical and chemical properties of these lakes did not differ much.     

Picoplankton photosynthesis and diurnal variations in photosynthesis-irradiance relationship in a eutrophic and meso-oligotrophic lake

The abundance and relative importance of autotrophic picoplankton were investigated in two lakes of different trophic status. In the eutrophic lake, measurements of primary production were performed on water samples in situ and in a light incubator three times during the day whereas for the oligotrophic lake, only one measurement of primary production was performed on water samples in the incubator. Dark-carbon losses of phytoplankton from Lake Loosdrecht were investigated in time series. Cell numbers of autotrophic picoplankton in eutrophic Lake Loosdrecht (3.2 × 10⁴ cells ml^–1) were lower than in meso-oligotrophic Lake Maarsseveen (9.8 and 11.4 × 10⁴ cells ml^–1 at the surface and bottom respectively). In the phytoplankton of both lakes the ratio of picoplankton production increased with decreasing light intensity. In Lake Loosdrecht depth-integrated contribution of picoplankton to total photosynthesis was less than 4%. The P-I-relationship showed diurnal variations in light saturated photosynthesis, while light limited carbon uptake remained constant during the day. Dark carbon losses from short-term labelled phytoplankton during the first 12 hours of the night period accounted for 10–25% of material fixed during the preceeding light period.     

Effects of water-column mixing on bacteria,phytoplankton, and rotifers under different levels of herbivory in a shallow eutrophic lake

Water-column mixing is known to have a decisive impact on plankton communities. The underlying mechanisms depend on the size and depth of the water body, nutrient status and the plankton community structure, and they are well understood for shallow polymictic and deep stratified lakes. Two consecutive mixing events of similar intensity under different levels of herbivory were performed in enclosures in a shallow, but periodically stratified, eutrophic lake, in order to investigate the effects of water-column mixing on bacteria abundance, phytoplankton abundance and diversity, and rotifer abundance and fecundity. When herbivory by filter-feeding zooplankton was low, water-column mixing that provoked a substantial nutrient input into the euphotic zone led to a strong net increase of bacteria and phytoplankton biomass. Phytoplankton diversity was lower in the mixed enclosures than in the undisturbed ones because of the greater contribution of a few fast-growing species. After the second mixing event, at a high biomass of filter-feeding crustaceans, the increase of phytoplankton biomass was lower than after the first mixing, and diversity remained unchanged because enhanced growth of small fast-growing phytoplankton was prevented by zooplankton grazing. Bacterial abundance did not increase after the second mixing, when cladoceran biomass was high. Changes in rotifer fecundity indicated a transmission of the phytoplankton response to the next trophic level. Our results suggest that water-column mixing in shallow eutrophic lakes with periodic stratification has a strong effect on the plankton community via enhanced nutrient availability rather than resuspension or reduced light availability. This fuels the basis of the classic and microbial food chain via enhanced phytoplankton and bacterial growth, but the effects on biomass may be damped by high levels of herbivory. Received: 3 May 1999 / Accepted: 13 April 2000     

Comparing microscopic counts and pigment analyses in 46 phytoplankton communities from lakes of different trophic state

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Fossil record of cladoceran and algal responses to fishery management practices

1. We hypothesized that the fishery management practices of toxaphene application and trout stocking would affect non-target organisms in lakes. Because these practices were rarely monitored in the past, cladoceran and algal assemblages were quantified in sediment cores from two lakes treated 30+ years ago to determine the long-term response of organisms near the base of the food chain. 2. Chydorids were remarkably resistant over the short term (a few years) in both the oligotrophic and eutrophic lakes despite toxaphene treatments that extirpated native fish and other invertebrates. In the oligotrophic lake (Annette Lake), six chydorid taxa were less abundant in the years following treatment, although no loss of species richness was detected. In the eutrophic lake (Chatwin Lake), the dominant Chydorus cf. sphaericus declined coincident with toxaphene treatment, but longer-term declines of all taxa were probably related to food web or other changes rather than to toxaphene toxicity. Cause and effect coupling was complicated by the fact that many chydorids were present at low concentrations in some pretreatment samples. 3. The algal communities (as fossil pigments) responded to treatment differently in the two lakes. In the oligotrophic lake, planktonic diatoms, dinoflagellates and chlorophytes were replaced as dominants by deep-water or benthic blooming cryptophytes, chrysophytes and cyanobacteria. This shift occurred along with increases in large daphnids and the ‘grazing indicator’, pheophorbide a. While both lakes appear to have had enhanced pigment preservation following treatment, the eutrophic lake encountered few long-term changes in its fossil pigment assemblage. Redundancy analysis estimated that the presence or absence of stocked trout explained much of the variation in the algal assemblages, particularly in the oligotrophic lake. 4. Toxaphene remained elevated in profundal sediments from these lakes 30 and 35 years after treatment.