This phytoplankton study was conducted from May to September 2002, 2003 and 2005 during fountain-based water aeration in the pelagial of Jeziorak Mały urban lake in Poland. Differences in the abundance and biomass of phytoplankton groups (cyanobacteria, diatoms, chlorophytes, dinoflagellates, chrysophytes and cryptomonads) related to physico-chemical water parameters were analyzed at the fountain and in the lake centre. Fountain water-mixing changed phytoplankton growth likely by decreasing water temperature, oxygenation and nutrient concentrations. These induced a disturbance in the cyanobacteria and stimulated growth of phytoplankton groups in the water column. High phytoplankton abundance at 1 m depth at the fountain could relate with phytoplankton sinking in the water column. This additional water mixing also intensified sedimented organic matter decomposition, thus enhancing nutrient uptake by phytoplankton. These results are important for future shallow urban lake management.
The paper aimed to get the analysis of spatial horizontal distribution of summer phyto-plankton in a small and shallow lake (Głębokie, Western Polesie, CE Poland) in relation to wind conditions occurring during the research period. The study was conducted in 2011 from 5th of July to 5th of September with eight sampling dates between. Water was sampled in the littoral zone from the depth of 0.5 m in four sites situated in different and opposite to one another lake shores. We analyzed the phytoplankton abundance by the way of chlorophyll a determination as well as the community taxonomic structure. Our research revealed that: a) the direction of the wind, which occurred during sampling might have an important role in the horizontal distribution of planktonic algal biomass within the lake; b) the geomorphology of lake surroundings probably mitigated the influence of wind on phytoplankton distribution; c) even weak or mild wind may influence phytoplankton horizontal differentiation.
Suspended matter, phytoplankton and light attenuation were investigated in various North East Greenland, Svalbard and Siberian river mouths in 1992-1994. The amount of mineral suspensions well correlated with freshwater discharge in the case of tidal glacier bays, while such correlation in Siberian rivers and pack ice meltwater was not found. Freshwater phytoplankton species were found in Siberian estuaries only and in two other ecosystems marine and ice phytoplankton species prevailed. The light attenuation connected with freshwater discharge seems to be a key factor limiting primary production in coastal Actic waters in the summer. The amount of glacial suspensions well correlated with the salinity drop in the case of Svalbard, while Siberian river estuaries produced very turbid waters with the suspension loads not correlated to freshwater or depth.
Within the SIBEX study area greater concentrations of net-phytoplanklon biomass and numbers were found in waters with clearly defined physical characteristics of either Bellingshausen Sea (an area north and west of Anvers Island and northern part of the Bransfield Strait) or Weddell Sea (south eastern entrance to the Bransfield Strait). Low biomass and cell numbers occurred in the southern Drake Passage and in the south central Bransfield Strait, which in the latter case, appears to be a characteristic feature of ihsse waters during the entire phytoplankton growing season. Early summer blooms of Chaetoceros neglectus and C. tortissimum were mainly responsible for high values of phytoplankton biomass. Some diatoms, such as C. socialis were exclusively associated with Weddell Sea water; a replacement of one water type by another in the Bransfield Strait may considerably modify phytoplankton populations which are present there.
Results of an oceanographic survey along the edge of drifting pack ice in the area between Elephant Island and the South Orkney Islands are reported. The influence of sea ice on hydrological factors was very weak. It was not possible to develop oceanographic features characteristic for marginal sea-ice zones in the areas with well marked surface currents and dynamic hydrological conditions. The spatial distribution of chlorophyll was governed by water stability, although during our survey, areas with enhanced vertical stability could not be described in terms of a sea-ice edge influence.
The highest concentrations of algal cells (1.1 x l0 6 litre- 1 ) and of algal carbon (20 μg litre -1 ) were associated with a lens of ice melt water in the northeast of the study area. Phytoflagellates were dominant at all stations with greater numbers always in the 0 - 20 m surface layer and with the peaks of Cryptophyceae in the open waters and also near the ice edge east of 50° W. Picoplankton flagellates and monads (1.5-5.0 μ) were generally next in abundance and most important numerically in the near ice stations in the western part of the study area. Parasinophyceae were usually more abundant than Nitzschia cylindrus (Grunow) Hasle, the only common diatom species found mainly in the western near ice edge stations. The presence olN.cylindrus, dominant in the pack ice and in phytoplankton near the ice edge, shows that algae released from ice may act as an inoculum for the phytoplankton.
Exposure of green algae Chlorella vulgaris to short-term UV-B radiation (280 nm – 315 nm) induced several changes in the function of photosystem II (PS II) studied by means of chlorophyll fluorescence (FL) and oxygen evolving. The intensity of photosynthetic oxygen evolving intensity of algae suspension decreased in a similar way to the FL parameter values in proportion to the applied dose of UV-B radiation (0.0, 3.2, 6.4, 12.8 kJ·m-2). The correlation between photosynthetic oxygen evolving intensity and FV/FO ratio was better than that between photosynthetic oxygen evolving intensity and FV/FM. The vitality index (Rfd) in the UV-B irradiated algae strongly decreased, compared to the control, which indicates inhibition of potential CO2 fixation and cooperation between light and dark reactions of photosynthesis. It may indicate damage of Rubisco.
According to the general classification of shallow eutrophic lakes, two alternative types are distinguished: phytoplankton-dominated and macrophyte-dominated lakes. The latter type is rare and currently endangered by human activity. In order to determine the effect of reduced inflow of surface water by an earth dyke on the lake trophic state, certain biological and physico-chemical parameters were evaluated. This work focuses on two lakes of similar morphometric characteristics situated in the agricultural landscape. The effect of the earth dyke on the trophic state was positively verified. The lake situated in the catchment basin, in which the inflow of surface water was reduced, was defined as meso-eutrophic, with a small amount of phytoplankton and high water transparency. The reference lake was highly eutrophic, with low water transparency and a large amount of phytoplankton. The water body surrounded by the earth dyke was macrophytes dominated (65% of the lake area), whereas the reference lake was a phytoplankton-macrophyte type (42% of the lake area). The trophic evaluation of a lake can be underestimated because of a significant amount of biogenic compounds accumulated in plant tissues. Thus, the values of Carlson’s indices in macrophyte-dominated lakes may not account for the total amount of nutrients in the water body.
Surface phytoplankton samples were studied quantitatively and qualitatively in February 1996 - November 1998 and January 2003 - November 2005 at the shore and in the center of Admiralty Bay, King George Island. Phytoplankton assemblages showed spring-summer peaks (maxima 4.0-5.2×106 cells l-1) associated with small variations in low atmospheric pressure, and low velocity winds. They were dominated by nano-sized (<20 µm) flagellates and picoplankton (~2 µm). The prevalent nanoflagellates were either Prasinophyceae, Cryptophyceae, or Prymnesiophyceae. Diatoms were next in abundance. Of the seven spring-summer diatom blooms, five had initiated at the shore (maximum 9.8×105 cells l-1; November 1998). They were significantly greater than in the open water, and did not spread into the bay centre. Two observed open water blooms did not reach the shore. Diatoms formed up to 44% of the total cells in the period 1996-98; they only formed <5% in 2003-05. Shore and open water populations differed by diatom dominance structure. Pennates (Fragilariopsis spp., F. cylindrus, Pseudo-nitzschia spp.), and benthic species were prevalent at the shore; centrics (Thalassiosira spp., Chaetoceros socialis) were most common offshore. In 2003-05 diatoms were relatively impoverished in Chaetoceros spp. and the larger (>20 µm) Fragilariopsis spp. Nano-sized Thalassiosira spp. were the winter dominants. Diatom species dominance structure may change at each of the two sites within a month (e.g. shore site: F. cylindrus dominant in October ’98; T. gravida in November ’98). Dinoflagellates showed summer increases associated with diatom blooms. Variations in phytoplankton cell concentrations, the species structures between the shore and open waters, and between seasons appear to be related to physical factors: changes in wind velocity and direction, inflow of waters from the Bransfield Strait, ice melting and changes in atmospheric pressure.
A total of sixty five taxa of marine phytoplankton (diatoms, dinoflagellates, silicoflagellates and cyanoprokaryotes) were recorded in the transect from the cold region of the Antarctic (Weddell Sea) up to La Plata Bay, Argentine in the late austral summer (March 1989). Diatoms were the dominant group in a south-north transect from the Seal-Bay (Princess Martha Land, the Antarctic). Most of the phytoplankton species of the cold Antarctic region disappeared around 50°S where there is a steep water temperature gradient. The diatom flora declined in the regions of increasing temperature, i.e. between 60° and 50° S and was replaced by dinoflagellates of the genus Ceratium. Large centric diatom genera Corethron, Rhizosolenia, Chaetoceros and Dactyliosolen represented the most apparent phytoplankton part. The most common of the small centric diatom genera were Thalassiosira, Asteromphalus, Actinocyclus and Coscinodiscus, while several species of Navicula and Nitzschia were the most abundant pennate forms. The presence of a considerable number of freshwater pennate diatoms, characterized as indifferent in the halobion spectrum and mostly periphytic, might be attributed to survival strategies during their development on the floating coastal ice.
In the region of Bransfield Strait and southern part of Drake Passage the highest amounts of chlorinated hydrocarbons (CHs — compounds of the DDT group, HCH isomers and PCBs) were found in the samples taken at the sampling station where the CHs bottom deposits were released to the upper layers due to the special hydrological situation at this station. Increased amounts of CHs were observed also in phytoplankton sampled close to the melting ice of glacier origin which was considered as a source of pollution. However, phytoplankton sampled from the waters covered with pack-ice exhibited the lowest rate of CHs accumulation. Slightly elevated CHs accumulation was found in sea ice diatoms. All the samples exhibited elevated amount of polichlorinated biphenyls, markedly higher than that of chloroorganic insecticides.
Phytoplankton sampling from 13 stations situated in Admiralty Bay was carried out in March. April, May, October and November 1983. Wet settling volume of seston, its dry weight, number of cells under 1 m2 , and qualitative composition of phytoplankton were determined. It was found that amount of phytoplankton was decreasing in April and increasing again in November after the winter season. The share of benthic and periphyton species in the qualitative composition of phytoplankton was quite significant, whereas their quantitative share was rather small. 163 taxa of algae were identified in the net phytoplankton; among these 107 taxa were reported for the first time from the Admiralty Bay. Most abundantly met throughout the entire study period were: Corethron criophilum and Thalassiothrix antarctica.
Phytoplankton samples were collected at 62 stations in the European Arctic Seas and the Faroe — Shetland Islands area. Over 30 species of dinoflagellates were found. 22 species are illustrated by original drawings. The data on synonyms, size or size variability on the distribution and environmental factors (temperature and salinity) are given.
A year-round (3 March 1994 - 28 February 1995) phytoplankton study in Admiralty Bay revealed nanoplankton flagellates (< 20 μm) to be the major algae of the plankton, both in terms of cell numbers and carbon biomass. Their quantities fluctuated widely thoroughly the year showing several peaks, in May, April, December and January. Summer maximum of the group in December was mainly due to Cryptophyceae (4.9 x 106 cells l-1; 98.0 μg C 1-1) and Prasinophyceae (7.3 x 105 cells -1; 33.5 μg C -1). Diatoms were usually scarce (max. 6.8 x 105 cells -1; 7.82 p:g C 1-1) and were dominated by small species of Thalassiosira and by Nitzschia spp. (Pseudonitzschia); the domination structure somewhat differed from that observed in Admiralty Bay in the summer of 1977/78. Algal peaks were related to the surface water (4 m depth) temperature rise from +0.16 to +1.71˚C. Summer phytoplankton maxima were about 5-fold greater than those recorded in the summer of 1977/78.
Phytoplankton samples were collected at 74 stations in the European Arctic seas, 28 species of the armoured din oft age Hates being found. Thirteen dinoflagellates are illustrated by original drawings. The data on synonyms, size or size variation, localities and environmental factors (temperature and salinity) at the surface are given.
Vertical distribution and quantitative and qualitative phytoplankton composition were studied in Ezcurra Inlet, Admiralty Bay, South Shetland Islands in the austral summer 1977/78. Nannoplankton flagellates, 12—15 μm in diameter and 4—6 μm "monads" were the principal algae of the plankton. Diatoms, present in a low abundance, were dominated by Thalassiosira antarctica and several species of the genera Nitzschia and Chaetoceros. Peaks of cell numbers within the 1—10 m surface stratum and at the bottom of the euphotic zone were characteristic of the vertical distribution of phytoplankton. Light, water movements and density micro-gradients were the likely factors controlling the vertical distribution of algae.
Fjords of West Spitsbergen are very dynamic in terms of hydrology. Here we tested whether the qualitative analysis of the taxonomic composition of phytoplankton may be useful as a fast method to assess the origin of the waters and whether it can give any additional information to hydrological data. Phytoplankton samples were collected along transects in Hornsund and Kongsfjord. Among total of 109 taxa identified, only 49 were common in both fjords. The assemblages in Hornsund implied that inflow of the cold waters of the Sřrkapp Current had occurred some time before samples collection, while in Kongsfjord the taxonomic composition was typical for the summer and did not show any recent, unusual hydrological phenomenon. Concluding, the method can be useful in the surveys in which hydrological data are collected infrequently.
Phytoplankton samples were collected at 141 stations in the Norwegian, Greenland, Barents and Baltic seas, in July-August 1992 and July-August 1993. In fifteen of these stations 22 unarmoured dinoflagellate species from the order Gymnodiniales belonging to the genera Amphidinium, Cochlodinium, Gymnodinium, Gyrodinium, Torodinium and Polykrikos have been found. Data on 16 species are given here, including synonyms, size or size variation, localities and environmental factors (temperature and salinity at the surface). 14 species are illustrated.
Altogether 105 algal taxa were identified including 101 diatom species. Chaetoceros criophilus was dominant in the western part of the study area influenced by waters from the Bellingshausen Sea. Corethron criophilum was abundant in the Weddcll Sea water mass found to the east of 53.5°W meridian. Nitzschia cylindrus common in the ice-melt samples was dominant in only two net phytoplankton collections obtained at the ice-edge zone. Additional samples from Admiralty Bay, at King George Island revealed the dominance of Chaetoceros socialis and the presence of many tychoplankton species. Very few diatom cells were found in the open waters of the Bransfield Strait which combined with the presence of krill, suggested intensive grazing by herbivores. The unstable waters of the Weddell-Scotia Confluence area contained little phytoplankton except for a station dominated by Phaeocystis pouchetii. Greater cell densities were related to warm, lower salinity Weddell Sea water of summer modification found in the surface layer east from 49°W.
Net phytoplankton cell numbers in 50 m water column of Admiralty Bay ranged between 0.2 x 10 5 x m-2 on 24 August 1990 and 2.3 x 10 7 x m-2 on 15 November 1990. Cluster analysis has confirmed the presence of two groups of samples: spring and summer ones (October to April), rich in cells and in species, and, on the other hand, winter samples (June to August) impoverished in algae. Spring and summer fluctuations of diatoms were mainly due to Corethron criophilum, Rhizosolenia alata and its varieties, R. hebetata f. semispina, Thalassiosira spp., Chaetoceros spp., and Nitzschia spp. (Fragilariopsis and Pseudonitzschia groups). The abundance and succession of species in Admiralty Bay reflect seasonal differences in diatom growth; they also reflect mixed populations of the Weddell and Bellingshausen seas entering Admiralty Bay via Bransfield Strait. Striking poverty of algae in some summer samples can most likely be attributed to zooplankton grazing.
In general, Antarctic marine bacteria are small, with biovolumes ranging from 0.139 to 0.204 μm-3 cell-1, but their total biomass in seawater is considerable due to relatively high numbers that approximate to 1020 cells km-3. Bacterial biomass becomes more concentrated closer to land. Our multi-year Antarctic studies demonstrated an average total bacterial biomass of 504 tons in Admirality Bay (24 km3) or 21 tons per 1 km3, versus 6.4 tons per 1 km3 in the open ocean. Strikingly, bacterial biomass reached 330 tons per 1 km3 of seawater at the sea-ice edge, as sampled in Goulden Cove in Admiralty Bay. Bacterial biomass in Admirality Bay, which we believe can be enriched by halotolerant and thermotolerant fresh water bacteria from glacial streams, is equal to or even exceeds that of the standing stock of krill (100-630 tons per bay) or other major living components, including phytoplankton (657 tons), flagellates (591 tons), and ciliates (412 tons). However, the bacterial biomass is exceeded by several orders of magnitude by non-living organic matter, which constitutes the basic bacterial carbon source. Factors regulating high bacterial abundance in the vicinity of land are discussed.