Peculiarities of summer phytoplankton spatial distribution in Onega Bay of the White Sea under local hydrophysical conditions

The species composition and phytoplankton biomass, concentrations of chlorophyll “a” (Chl) and nutrients in the surface water layer, and accompanying hydrophysical conditions were studied in Onega Bay of the White Sea in June 2015. The temperature and salinity of surface water layer and the water column stability varied greatly in the bay. The nutrients' concentrations exceeded the limiting threshold necessary for the phytoplankton development. The phytoplankton abundance was relatively low, averaged as 13.46 ± 9.00 mg C/m³ (total phytoplankton biomass), 0.78 ± 0.43 mg/m³ (concentration of chlorophyll “a”), and 0.18 ± 0.27 mg C/m³ (picophytoplankton biomass). The highest phytoplankton biomass has been registered along the frontal zones. Three phytoplankton communities that differed significantly in their structure have been found.     

Interannual variability in the distribution of the phytoplankton standing stock across the seasonal sea-ice zone west of the Antarctic Peninsula

The spatial distribution of phytoplankton cell abundance, carbon(C) biomass and chlorophyll a (Chl a) concentration was analysedduring three summers (1996, 1997 and 1999) in a seasonal sea-icearea, west of the Antarctic Peninsula. The objective of thestudy was to assess interannual variability in phytoplanktonspatial distribution and the mechanisms that regulate phytoplanktonaccumulation in the water column. Phytoplankton C biomass andChl a distributions were consistent from year to year, exhibitinga negative on/offshore gradient. The variations in C concentrationhad a close and non-linear relationship with the upper mixedlayer depth, suggesting that the vertical mixing of the watercolumn is the main factor regulating phytoplankton stock. Themagnitude of C gradients was 5-fold higher during 1996 thanduring 1997 and 1999. This was ascribed to interannual variationsin the concentration of diatom blooms in the region influencedby sea-ice melting. Vertical distribution of the phytoplankton,as estimated from Chl a profiles, also varied along an on/offshoregradient: Chl a was distributed homogeneously in the upper mixedlayer in coastal and mid-shelf stations and concentrated inthe deep layer (40–100 m) occupied by the winter waters(WW, remnants of the Antarctic surface waters during summer)in more offshore stations. The region with a deep Chl a maximumlayer (DCM layer) was dominated by a phytoplankton assemblagecharacterized by a relatively high concentration of diatoms.The extent of this region varied from year to year: it was restrictedto pelagic waters during 1996, extended to the shelf slope during1997 and occupied a major portion of the area during 1999. Itis hypothesized that iron depletion in near surface waters dueto phytoplankton consumption, and a higher concentration inWW, regulated this vertical phytoplankton distribution pattern.Furthermore, we postulate that year-to-year variations in thespatial distribution of the DCM layer were related to interannualvariations in the timing of the sea-ice retreat. The similaritybetween our results and those reported in literature for otherareas of the Southern Ocean allows us to suggest that the mechanismsproposed here as regulating phytoplankton stock in our areamay be applicable elsewhere.     

Phytoplankton community structure derived from HPLC analysis of pigments in the Faroe-Shetland Channel during summer 1999: the distribution of taxonomic groups in relation to physical/chemical conditions in the photic zone

A study of the phytoplankton community in the Faroe-ShetlandChannel was conducted in July 1999. Samples were collected atvarious depths in the photic zone along three transects (thenorthern entrance, the center and the southern entrance). Exceptfor a few easterly stations where nitrate and silicate werebelow 1 µM, all nutrients (phosphate, silicate, ammonium,nitrite and nitrate) were non-limiting for phytoplankton growth.HPLC pigment analysis revealed a pronounced (>50%) dominanceof Prymnesiophyceae at all stations. Their pigment ratio ofdiatoxanthin + diadinoxanthin/Chl a (DDX/Chl a) indicated thatthe phytoplankton community was controlled by light. Primaryproduction in the delayed spring bloom varied from 1.2 to 1.8g C m^–2 day^–1 along the northern transect. Alongthe other two transects, primary production ranged from 1.6to 3.8 g C m^–2 day^–1. Associated with the characteristicsindicating the establishment of a bloom, the relative contributionof diatoms and Prymnesiophyceae increased, whereas that of Prasinophyceae,Cryptophyceae, Chrysophyceae and Cyanobacteriaceae decreased.With respect to their vertical distribution, Cyanobacteriaceae,Chrysophyceae and Dinophyceae tended to have a higher abundance,relative to other taxonomic groups, in the surface layers. Therelative abundance of diatoms and Chlorophyceae increased withdepth. The DDX/Chl a ratio of the Prymnesiophyceae decreasedwith depth, indicating that vertical mixing in the upper 30m of the photic zone occurred less frequently than the timespan of physiological acclimation of cellular pigment composition.     

Chlorophyll <Emphasis Type="Italic">a</Emphasis> as a measure of seasonal coupling between phytoplankton and the monsoon periods in the Gulf of Oman

We present data from a long time-series study to describe the factors that control phytoplankton population densities and biomass in the coastal waters of Oman. Surface temperature, salinity, nutrients, dissolved oxygen, chlorophyll a (Chl a), and phytoplankton and zooplankton abundance of sea water were measured as far as possible from February 2004 through February 2006, at two stations along the southern coast of the Gulf of Oman. The highest concentrations of Chl a (3 mg m⁻³) were recorded during the southwest monsoon (SWM) when upwelling is active along the coast of Oman. However, results from our study reveal that the timing and the amplitude of the seasonal peak of Chl a exhibited interannual variability, which might be attributed to interannual differences in the seasonal cycles of nutrients caused either by coastal upwelling or by cyclonic eddy activity. Monthly variability of SST and concentrations of dissolved nitrate, nitrite, phosphate, and silicate together explained about 90% of the seasonal changes of Chl a in the coastal ecosystem of the Gulf of Oman. Phytoplankton communities of the coastal waters of Oman were dominated by diatoms for most part of the year, but for a short period in summer, dinoflagellates were dominant.     

Distribution and development of under-ice phytoplankton in 90-m deep water column of Lake Päijänne (Finland) during spring convection

Distribution and development of phytoplankton were studied in the deep and large Lake Päijänne from mid-winter until the disappearance of ice. Diatoms were an important part of the phytoplankton assemblage and, with cryptophytes and chrysophytes, made up 50–80% of the phytoplankton biomass. In mid-winter, chlorophyll a and phytoplankton biomass were uniformly distributed over the whole water column down to a depth of 90 m. Thus, most of the phytoplankton was in virtual darkness and there was negligible growth. Only motile cryptophytes were concentrated in the layers below the ice and were rare in deep water. After the disappearance of snow, convection developed, but at first cryptophytes were able to resist mixing. When convection turned from penetrative to predominantly horizontal, all phytoplankton were generally uniformly distributed in the water column. In spite of the full under-ice overturn with low average availability of light, the phytoplankton biomass doubled in April. The growth of cryptophytes was higher than that of diatoms, suggesting that motile species gained an advantage by being able to maintain themselves in the upper, illuminated layers. The results show that knowledge of the basic physical framework is essential for interpretation of under-ice phytoplankton results.     

Hydrography and characteristics of the phytoplankton in shelf and oceanic waters off southeastern Brazil during winter (July/August 1982) and summer (February/March 1984)

The physical and chemical environment, and the phytoplankton primary production of southeastern Brazil were studied in relation to the general oceanographic structure during two research cruises (winter and summer). In each cruise, a total of 91 stations were occupied. Data were collected on the spatial distribution of nutrients, phytoplankton biomass and photosynthetic capacity over the coastal, shelf and oceanic areas off São Paulo, Paraná and Santa Catarina States.During wintertime, the mixing processes between tropical warm waters of the Brazil Current and subantarctic waters of the Malvinas Current formed strong environmental gradients. The drainings of Rio de La Plata and Lagoa dos Patos are transported northwards by coastal currents, enriching the shelf waters off Santa Catarina State with inorganic nutrients and consequently increasing the chlorophyll a to the highest concentrations (> 3.5 mg m ^–3) measured during the two cruises. In slope waters chlorophyll values were always low (0.05–0.45 mg m ^–3). The chlorophyll within the euphotic layer varied from 8.8–36.7 and 1.2–18.5 mg m^–2 during winter and summer, respectively.The surface photosynthetic rates during winter and summer cruises ranged respectively from 0.21–9.17 and 0.66–19.60 mgC/mgChl.a/h. The mean rates were higher in nearshore waters and decreased seaward.The thermal structure of the water column affected the vertical distribution of chlorophyll a and photosynthesis within the euphotic zone; During unstratified periods (winter) they were uniformly distributed but the occurrence of subsurface peaks of chlorophyll and strong photosynthetic inhibition of low light adapted cells in deeper layers are associated to the seasonal thermocline. Occasionally, upwelling of deep waters from shelf break enriched the deeper euphotic layers in offshore areas. Intensive upwelling was observed off Paranagua Bay (Parana State) and the mechanisms of its formation are discussed.     

Algal respiration and the regulation of phytoplankton biomass in a polymictic tropical lake (Lake Xolotlán,Nicaragua)

Community respiration in tropical Lake Xolotlán, Nicaragua, was assessed seasonally and during diurnal cycles, via oxygen consumption in bottle enclosures. Results were analysed in relation to phytoplankton biomass, mixing depth, depth of photic zone and phytoplankton production. A great part of community respiration was associated with the heterotrophic activity of the phytoplankton biomass or its degradation by bacteria and 80% of the variability in oxygen consumption was explained by the variation of chlorophyll-a. Specific rate of respiration was 1.5 mg O2 mg Chla-1 h-1 during diurnal cycles, which corresponded to less than 5% of the specific rate at optimum depth of production. Still, diurnal water column respiratory losses were always of the same magnitude as the total photosynthetic gains in the photic zone, since the mixing depth exceeded the depth of the photic zone. Total column net growth was zero at a ratio between depth of photic zone and mixing depth of 0.19. Water level variations however altered the mixing depth and affected this ratio and net growth. As a consequence, the phytoplankton biomass either increased or decreased until the ratio was re-established through changes of the photic zone depth, which was governed by the phytoplankton biomass itself through the chlorophyll-a light attenuation. This revised version was published online in July 2006 with corrections to the Cover Date.     

Long‐term phytoplankton community changes in a deep subalpine lake: responses to nutrient availability and climatic fluctuations

1. In natural lakes, modifications in the species composition and abundance of phytoplankton communities may ultimately be responses to changes in nutrient availability and climatic fluctuations. Phytoplankton and associated environmental factors were collected at monthly intervals from the beginning of the 1990s to 2007 in the large subalpine Lake Garda (z_max = 350 m, V = 49 × 10⁹ m³). In this study period, the lake showed a slight and continuous increase of total phosphorus (TP) in the water column, up to concentrations of 18–20 μg P L^?1. This increase represented the last stage of a long‐term process of enrichment documented since the 1970s, when concentrations of TP were below or around 10 μg P L^?1. 2. At the community level, annual phytoplankton cycles underwent a unidirectional and slow shift mainly due to changes in the species more affected by the nutrient enrichment of the lake. After a first and long period of dominance by conjugatophytes (Mougeotia) and diatoms (Fragilaria), phytoplankton biomass in recent years was sustained by cyanobacteria (Planktothrix). Other important modifications in the development of phytoplankton were superimposed on this pattern due to the effects of annual climate fluctuations principally mediated by the deep mixing events at spring overturn and, secondarily, by temperature and thermal stability of the water column during the growing season. 3. Interannual variations in the stability and temperature of the water column appeared to influence the development of a few subdominant flagellates (dinophytes and cryptophytes). Nevertheless, the major impact of climate on phytoplankton was indirect, and mediated through the effects of winter climatic conditions on deep mixing dynamics. Winter climatic fluctuations proved to be a key element in a linked chain of causal factors including cooling of hypolimnetic waters, deep vertical mixing and epilimnetic nutrient replenishment. The process of fertilisation was measurable both for TP and dissolved inorganic nitrogen, although only the first had a large effect, reinforcing the seasonal growth of a few dominant groups. The degree of nutrient replenishment further increased the spring development of large diatoms and the increase of Planktothrix in summer and autumn. 4. Currently, changes in nutrient concentrations have the greatest effect on the phytoplankton community, while direct effects due to the interannual variations in the thermal regime are of secondary importance compared with the indirect effects mediated through deep water mixing and spring fertilisation. Overall, the results demonstrate that the consequences of climatic fluctuations and climate warming on phytoplankton communities need to be studied at different levels of complexity and integration, from the direct effects of temperature and thermal regime, to the indirect effects mediated by the physiographic characteristics of water bodies.     

Artificial destratification of a small tropical reservoir: effects upon the phytoplankton

Seasonal changes in the phytoplankton community of a small tropical reservoir were monitored over a four year period comprising of an initial two seasonal cycles during which the water column stratified strongly for extended periods each year, and two further seasonal cycles after installation of a mechanical aeration system to induce artificial destratification. In the unmanaged reservoir, the concentration of chlorophyll a at 0.5 m reached maximum values (on one occasion > 90 mg m⁻³) when the water column was stratified and the epilimnion was very shallow (ca 2 m depth). The hypolimnion at this time was anoxic (less than 2% oxygen saturation) and had a high concentration of bacteriochlorophyll (100–200 mg m⁻³). The phytoplankton community of the unmanaged reservoir was generally dominated by cyanobacteria (Cylindrospermopsis raciborskii, Anabaena tenericaulis) during the warmer months of the year (November–March) (but replaced by chlorophyta, dinophyceae and euglenophyceae after periods of intense rain) and by bacillariophyceae (Synedra ulna var. chaseana, S. tenera) during the cooler, dry months. In the artificially destratified reservoir (8 h aeration day⁻¹), the phytoplankton community was largely dominated by diatoms except after depletion of the silica content of the water column which caused diatoms to be replaced by cyanobacteria (dominated by A. tenericaulis) and a range of chlorophytes. The changing pattern of stratification and circulation of the water column in the unmanaged reservoir caused repeated disruption of the established phytoplankton assemblage with peaks of high biomass associated with transient cyanobacterial blooms. Continuous aeration and the consequent increase in the ratio mixed: euphotic depth provided conditions suitable for dominance of the phytoplankton by diatoms, as long as silica was available, and resulted in average chlorophyll levels higher than in the unmanaged reservoir (120 ± 10 v. 64 ± 9 mg m⁻²). Hierarchical fusion analysis based on the biomass of species differentiated the phytoplankton samples into cluster groups that could be related primarily to stratification or mixing of the water column.     

Production in the Sea of Okhotsk

Primary production, microbial production and the density of planktonic microheterotrophs were estimated at 40 stations in the Okhotsk Sea in July-August 1992 during the seasonal phytoplankton minimum. The primary production by phytoplankton remained rather high even during this minimum. At most stations it was >0.6-0.8 g m^-2 day^-1, and in leftover patches of spring diatom 'bloom' it reached >5 g C m^-2 day^-1. The deep maxima of phytoplankton at the upper boundary of the seasonal thermocline were an ordinary phenomenon. The depth of the euphotic zone was normally 30-50 m in the open sea and 12-25 m at the shelf station. Any correlations between the phosphate contents in the upper mixed layer and primary production were absent at the stations. There was no adaptation of the phytoplankton to the light deficiency in deep maxima layers. The total numbers of bacterioplankton were 1-1.5 x 10⁶ ml^-1 and its biomass was close to 100 mg m^-3 in the open sea. All these numbers were 2-3 times greater at the shelf stations. In deep waters, the bacterioplankton biomass decreased to 10-40 mg m^-3. The microbial production in the upper layer was high, at 50-100 mg m^-3, decreasing 50-100 times in the deep waters. The numbers of ciliates in the upper water layer varied from 3 to 6 x 10³ l^-1 and were 1.5-2 times greater than in the shelf areas. Ciliate biomass was 60-100 mg m^-3 in the upper mixed layer, and per square metre varied to 1.5-2.5 g. The dominant ciliate taxa belonged to the naked oligotrichid genera Strombidium and Tontonia. Tentative calculations were made of the basin's annual primary production and for the analysis of energy balance in the ecosystem.      

Seasonal variability of phytoplankton populations in the middle Adriatic sub-basin

The seasonal variability of phytoplankton assemblages in themiddle Adriatic sub-basin is described. The investigated areacrossed the middle Adriatic from the Italian to the Croatiancoasts. Hydrographic data, chlorophyll (Chl) a and phytoplanktonwere collected on a seasonal basis from May 1995 to February1996. Highest phytoplankton densities (up to 6 x 10⁶ cells dm^–3)were observed in spring and autumn in the western side, withinthe diluted waters. The vertical distribution of Chl a exhibiteda pronounced subsurface maximum associated, in coastal waters,with micro-planktonic diatoms. Phytoplankton assemblages weredominated by phytoflagellates in all the periods investigated.Diatom maxima were observed in spring and autumn: their verticaldistribution generally reflected the Chl a pattern and in thewestern coastal area peaks are due to large diatom species (Pseudo-nitzschiaspp.). In offshore waters, dinoflagellates strongly prevailover diatoms and provide a relevant contribution to the totalbiomass, especially in highly stratified conditions. Coccolithophoridswere mostly encountered in surface layers and their highestcontribution to the total biomass was observed in the LevantineIntermediate Water.     

Ice algal assemblages and vertical export of organic matter from sea ice in the Barents Sea and Nansen Basin (Arctic Ocean)

Algal communities and export of organic matter from sea ice were studied in the offshore marginal ice zone (MIZ) of the northern Barents Sea and Nansen Basin of the Arctic Ocean north of Svalbard by means of ice cores and short-term deployed sediment traps. The observations cover a total of ten stations within the drifting pack ice, visited over a period of 3 years during the period of ice melt in May and July. Maximum flux of particulate organic carbon and chlorophyll a from the ice at 1 m depth (1,537 mg C m⁻² per day and 20 mg Chl a m⁻² per day) exceeded the flux at 30 m by a factor of 2 during spring, a pattern that was reversed later in the season. Although diatoms dominated the ice-associated algal biomass, flagellates at times revealed similarly high biomass and typically dominated the exported algal carbon. Importance of flagellates to the vertical flux increased as melting progressed, whereas diatoms made the highest contribution during the early melting stage. High export of ice-derived organic matter and phytoplankton took place simultaneously in the offshore MIZ, likely as a consequence of ice drift dynamics and the mosaic structure of ice-covered and open water characteristic of this region.     

Sedimentation in Arctic Canada: Species composition and biomass of phytoplankton contributed to the marine sediments in Frobisher Bay

Summary Sedimentation of phytoplankton provides food and energy for zoobenthic communities. In this study the rates, species composition and biomass of phytoplankton input to Frobisher Bay sediments were examined during ice (late November to July) and open water (late July to October) periods from 1982 to 1985. The rates were higher on the sea bed than at 20 m. The minimum rate (3x10⁵ cells·m^-2·day^-1) of sedimentation occurred during the early part of the ice period. It increased as the ice thickened and reached a maximum of 2.8x10⁸ cells·m^-2·day^-1 after the phytoplankton bloom at the beginning of the open water period in the first two weeks of August. The sedimented phytoplankton was dominated by diatoms, with a great majority of pennate species during the spring (April to June) and centric forms during the summer (July to August). Green flagellates, dinoflagellates and chrysophytes occurred as a low percentage of the total population in all seasons. Other indicators (chlorophyll a and phaeopigments) showed highest biomass levels in the deepest traps. They were consistently low during the winter (December to March) and reached their maxima during the open-water period of summer. Their abundance was correlated with the seasonal cycle of the phytoplankton in the water column.     

Physical-Biological Coupling in the Western South China Sea: The Response of Phytoplankton Community to a Mesoscale Cyclonic Eddy

It is widely recognized that the mesoscale eddies play an important part in the biogeochemical cycle in ocean ecosystem, especially in the oligotrophic tropical zones. So here a heterogeneous cyclonic eddy in its flourishing stage was detected using remote sensing and in situ biogeochemical observation in the western South China Sea (SCS) in early September, 2007. The high-performance liquid chromatography method was used to identify the photosynthetic pigments. And the CHEMical TAXonomy (CHEMTAX) was applied to calculate the contribution of nine phytoplankton groups to the total chlorophyll a (TChl a) biomass. The deep chlorophyll a maximum layer (DCML) was raised to form a dome structure in the eddy center while there was no distinct enhancement for TChl a biomass. The integrated TChl a concentration in the upper 100 m water column was also constant from the eddy center to the surrounding water outside the eddy. However the TChl a biomass in the surface layer (at 5 m) in the eddy center was promoted 2.6-fold compared to the biomass outside the eddy (p < 0.001). Thus, the slight enhancement of TChl a biomass of euphotic zone integration within the eddy was mainly from the phytoplankton in the upper mixed zone rather than the DCML. The phytoplankton community was primarily contributed by diatoms, prasinophytes, and Synechococcus at the DCML within the eddy, while less was contributed by haptophytes_8 and Prochlorococcus. The TChl a biomass for most of the phytoplankton groups increased at the surface layer in the eddy center under the effect of nutrient pumping. The doming isopycnal within the eddy supplied nutrients gently into the upper mixing layer, and there was remarkable enhancement in phytoplankton biomass at the surface layer with 10.5% TChl a biomass of water column in eddy center and 3.7% at reference stations. So the slight increasing in the water column integrated phytoplankton biomass might be attributed to the stimulated phytoplankton biomass at the surface layer.     

Winter condition of marine plankton populations in Saanich inlet,B.C., canada. I. Phytoplankton and its surrounding environment

Weekly sampling was carried out in Saanich Inlet, British Columbia throughout the winter of 1975–1976. The surface water column was characterized by exposure to low solar radiation energy (<150 g cal·cm^?2 · day^?1), slight stratification with occasional vertical mixing, and abundant algal nutrients. Phytoplankton were mostly distributed above 5 m in the water column, with a fairly low biomass averaging <1 μgchla·1^?1. Dominant phytoplankton organisms were nanoflagellates occasionally accompanied by dinoflagellates as the second dominant. Centric diatoms, which were dominant in the blooms, were always present but less than a few percentage of the total phytoplankton biomass. Daily photosynthetic productivity was exclusively limited by available radiant energy. Low solar radiation and occasional mixing of the surface zone prohibited the centric diatoms from becoming dominant.     

Multiple subsurface phytoplankton blooms occurring simultaneously in the Skagerrak

The distribution and characteristics of phytoplankton in theSkagerrak in August–September 2000 were analysed in orderto evaluate the importance of subsurface phytoplankton peaksto water column ecology and primary production. In areas affectedby outflow from the Baltic, enhanced chlorophyll concentrationswere found in the warm surface waters (i.e. upper 10–20m). However, for the central Skagerrak, the major part (50–80%)of the chlorophyll in the water column was found below the warmsurface waters. The highest chlorophyll concentrations (up to>18 µg l^-1) in the study area were also found belowthe warm surface waters and up to 95% of total water columnprimary production was recorded below the warm surface waterlayer. Measurements of variable fluorescence (F_v/F_m) indicatedthe greatest potential capacity for electron flow in photosystemII in phytoplankton was located below the warm surface waters.Spectrophotometrically determined pigment ratios suggest thatthe enhanced capacity for photosynthesis in the deeper watersmay be related to greater nutrient availability here than insurface waters. Subsurface chlorophyll distributions seen inrelation to the different water masses identified in the area,as well as community analysis of the phytoplankton present inthe subsurface peaks, indicate the presence of at least threedistinct subsurface phytoplankton blooms in the Skagerrak duringthe study period. Local oxygen saturation maxima recorded immediatelyabove the subsurface peaks provide in situ evidence that thesepeaks are photosynthetically active. This suggests that newproduction is taking place in these peaks, although quantificationof this production is hampered due to a lack of informationconcerning the initial conditions in and lifetime of the subsurfacepeaks. The subsurface phytoplankton peaks were, generally, foundimmediately above an oxygen minimum that covered the entirestudy area. In the relatively cold deep Atlantic water foundbelow the oxygen minimum layer, no or very little chlorophyllwas recorded and oxygen concentrations increased. Thus, it isargued that the respiration of the organic material producedin the upper part of the water column during late summer mayprimarily occur in the intermediate layers of the water column.     

Phytoplankton dynamics in the Congo River

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Build-up and decline of summer phytoplankton biomass in the eastern Weddell Sea,Antarctica

The seasonal development and decline of phytoplankton was investigated in the eastern Weddell Sea during summer and fall 1991. During the first half of the study (15 Jan–13 Feb) in an area off Vestkapp, favourable irradiance/mixing regimes initiated net phytoplankton growth in ice-free waters on the shelf and in stretches of open water over the partially ice-covered deep ocean. Chi a concentrations in the upper water column were moderate (0.2–0.8 g l^–1), but significantly above winter values. Later in the season (16 Feb–11 March), a phytoplankton bloom with surface Chl a concentrations ranging from 1.6–2.3 g l^–1 was encountered in an area further to the east. We suggest that the upper water column must have been stratified in this region for time scales of weeks to faciliate bloom development. Bacterial biomass and productivity generally paralleled the seasonal development of the phytoplankton. Nitrate concentrations in the upper mixed layer were substantially lower than would be expected from the existing phytoplankton standing stock, suggesting that heterotrophic consumption of organic matter by bacteria and zooplankton removed a large fraction of the primary production. The shallow seasonal pycnocline was eventually eroded by the passage of a storm, resulting in a homogeneous distribution of phytoplankton biomass over the entire water column, followed by sedimentation and deposition of phytodetritus on the sea floor. After the storm induced destratification, bacterial productivity was particularly high, amounting to more than half of the primary production (range: 10%–120%) in the upper water column. Subsequently, phytoplankton biomass in the upper water column decreased to values <1 g Chl a l^–1. The combination of low incident irradiances and incessant deep mixing prevented the phytoplankton biomass to increase again. During the last week of the investigation, extensive new-ice formation was observed. A major fraction of the residual surface plankton was incorporated into new sea ice, thus terminating the pelagic growth season of the phytoplankton in the eastern Weddell Sea.     

Spatial and temporal photosynthetic compartments during summer in Antarctic Lake Kitiesh

Summary Four autotrophic compartments were recognised in Lake Kitiesh, King George Island (Southern Shetland) at the beginning of the summer in 1987: snow microalgae, ice bubble communities, phytoplankton in the water column and benthic communities of moss with epiphytes. Chlorophyll a concentration and pigment absorption spectra were obtained in these four compartments before and/or after the thawing of the ice cover. During the ice free period, carbon fixation and biomass was measured in the phytoplankton and in the benthic moss Campyliadelphus polygamus. From these measurements we conclude that the benthic moss is the most significant autotrophic component in this lake in terms of biomass, chlorophyll a content and primary productivity. The integral assimilation number (The ratio of carbon fixation per unit area to biomass per unit area) values were similar for both phytoplankton and the moss, ranging from 3.6 to 5.4 mg C (mg Chl a)^–1h^–1in phytoplankton and from 4.0 to 6.4 mgC (mg Chl a)^–1h^–1 in the benthic moss. This approach allows comparisons of carbon fixation efficiency of the chlorophyll a under a unit area between compartments in their different light environments.     

Light limitation of phytoplankton development in an oligotrophic lake - Loch Ness, Scotland

• 1 The underwater light climate in Loch Ness is described in terms of mixing depth (Z_m) and depth of the euphoric zone (Z_eu). During periods of complete mixing, Z_m equates with the mean depth of the loch (132 m), but even during summer stratification the morphometry of the loch and the strong prevailing winds produce a deep thermocline and an epilimnetic mixed layer of about 30 m or greater. Hence, throughout the year the quotient Z_m/Z_eu is exceptionally high and the underwater light climate particularly unfavourable for phytoplankton production and growth.
• 2 Phytoplankton biomass expressed as chlorophyll a is very low in Loch Ness, with a late summer maximum of less than 1.5 mg chlorophyll a m^-3 in the upper 30 m of the water column. This low biomass and the resulting very low photosynthetic carbon fixation within the water column are evidence that a severe restraint is imposed on the rate at which phytoplankton can grow in the loch.
• 3 The chlorophyll a content per unit of phytoplankton biovolume and the maximum, light-saturated specific rate of photosynthesis are both parameters which might be influenced by the light climate under which the phytoplankton have grown. However, values obtained from Loch Ness for both chlorophyll a content (mean 0.0045 mg mm^-3) and maximum photosynthetic rate (1–4 mg C mg Chla^-1 h^-1) are within the range reported from other lakes.
• 4 Laboratory bioassays with the natural phytoplankton community from Loch Ness on two occasions in late summer when the light climate in the loch is at its most favourable, suggest that even then limitation of phytoplankton growth is finely balanced between light and phosphorus limitation. Hence, for most of the year, when the light climate is less favourable, phytoplankton growth will be light limited.
• 5 Quotients relating mean annual algal biomass as chlorophyll a (c. 0.5 mg Chla m^-3) and the probable annual specific areal loading of total phosphorus (0.4–1.7 g TP m^-2 yr^-1) suggest that the efficiency with which phytoplankton is produced in Loch Ness per unit of TP loading is extremely low when compared with values from other Scottish lochs for which such an index has been calculated. This apparent inefficiency can be attributed to suppression of photosynthetic productivity in the water column due to the unfavourable underwater light climate.
• 6 These several independent sources of evidence lead to the conclusion that phytoplankton development in Loch Ness is constrained by light rather than by nutrients. Loch Ness thus appears to provide an exception to the generally accepted paradigm that phytoplankton development in lakes of an oligotrophic character is constrained by nutrient availability.