Dynamics and Distribution of Cyanophages and Their Effect on Marine Synechococcus spp.

Cyanophages infecting marine Synechococcus cells were frequently very abundant and were found in every seawater sample along a transect in the western Gulf of Mexico and during a 28-month period in Aransas Pass, Tex. In Aransas Pass their abundance varied seasonally, with the lowest concentrations coincident with cooler water and lower salinity. Along the transect, viruses infecting Synechococcus strains DC2 and SYN48 ranged in concentration from a few hundred per milliliter at 97 m deep and 83 km offshore to ca. 4 × 10⁵ ml^-1 near the surface at stations within 18 km of the coast. The highest concentrations occurred at the surface, where salinity decreased from ca. 35.5 to 34 ppt and Synechococcus concentrations were greatest. Viruses infecting strains SNC1, SNC2, and 838BG were distributed in a similar manner but were much less abundant (<10 to >5 × 10³ ml^-1). When Synechococcus concentrations exceeded ca. 10³ ml^-1, cyanophage concentrations increased markedly (ca. 10² to > 10⁵ ml^-1), suggesting that a minimum host density was required for efficient viral propagation. Data on the decay rate of viral infectivity d (per day), as a function of solar irradiance I (millimoles of quanta per square meter per second), were used to develop a relationship (d = 0.2610I - 0.00718; r² = 0.69) for conservatively estimating the destruction of infectious viruses in the mixed layer of two offshore stations. Assuming that virus production balances losses and that the burst size is 250, ca. 5 to 7% of Synechococcus cells would be infected daily by viruses. Calculations based on contact rates between Synechococcus cells and infectious viruses produce similar results (5 to 14%). Moreover, balancing estimates of viral production with contact rates for the farthest offshore station required that most Synechococcus cells be susceptible to infection, that most contacts result in infection, and that the burst size be about 324 viruses per lytic event. In contrast, in nearshore waters, where ca. 80% of Synechococcus cells would be contacted daily by infectious cyanophages, only ca. 1% of the contacts would have to result in infection to balance the estimated virus removal rates. These results indicate that cyanophages are an abundant and dynamic component of marine planktonic communities and are probably responsible for lysing a small but significant portion of the Synechococcus population on a daily basis.     

Dynamics of phytoplankton detritus in a shallow,eutrophic lake (Lake Loosdrecht,The Netherlands)

A study was made of the mortality and aerobic decomposition of light- and phosphorus-limited cultures of Oscillatoria limnetica, a dominant phytoplankton species in shallow, eutrophic Lake Loosdrecht (The Netherlands). When placed in the dark at 20 °C, most cells died and lysed within twelve days. The labile organic matter was completely decomposed within three weeks. Absorbance spectra indicated that blue green algae may contributed significantly to the refractory dissolved substances in the lake. Refractory particulate matter constituted from 7 to 24% of the biomass of O. limnetica, depending on the growth rate before incubation in the dark. The decomposition rate of this fraction was 0.005 d^–1. On a basis of a steady-state model of the dynamics of phytoplankton detritus, the areal organic dry weight concentration of the detritus in the lake is ca. 60 g m^–2. This means the quantities of detritus in the seston and epipelon are about equal.     

Georgian Bay phytoplankton: Ecology and response to contaminants

The phytoplankton productivity of Georgian Bay was studied during 1974. Lakewide samples were collected at 16 stations during monthly cruises from April to December and identification and enumeration was carried out by the Utermohl technique. Contaminant bioassays with metals added singly and as a mixture were performed in 1980 and 1981. Based on an overall average, Diatomeae (36–73%) was the most prevalent component of phytoplankton biomass followed by Chrysophyceae (5–38%), and Cyanophyta (3–27%). Biomass means of all stations by cruise indicated a range of 0.35 to 0.61 g·m^–3 with a bimodal seasonal pattern. Although ultraplankton made the highest mean percent contribution to the biomass (37%), the other size assemblages such as < 5 µm (26%) and netplankton (29%) were not unimportant.Size fractionation of primary productivity during 1974 revealed that a major portion of photosynthesis (39–70%) was in the <20 µm size fraction. Algal Fractionation Bioassays conducted during 1980 and 1981 indicated a significant inhibition of ultraplankton productivity. Additional bioassays with single metals and in combination showed differential toxicity to various phytoplankton size assemblages.The phytoplankton biomass and floristic composition indicate the Georgian Bay ecosystem to be oligotrophic. This ecosystem appears to be controlled by the physical dynamics of thermal and flow regimes. Compared with other Great Lakes, the low P/B quotients recorded in oligotrophic Georgian Bay is enigmatic and may be attributable to the observed sensitivity of phytoplankton to contaminants originating from anthropogenic and natural sources.     

Phytoplankton dynamics and sedimentation processes during spring and summer in Balsfjord,Northern Norway

Summary Chlorophyll a, phytoplankton species composition and carbon (PPC) estimated from cell-counts, were monitored together with hydrographic parameters and nutrients in the upper 50 m of Balsfjord (ca. 70° N), northern Norway between 08 February and 29 June 1982. Sediment traps were placed at 10, 50, 100, and 170 m (10 m above bottom) for intervals of 5–20 days during the study period. Trap contents were analyzed for phytoplankton as above; dry weight, particulate organic material (POM), particulate organic nitrogen and carbon (PON and POC), ash, and particulate phosphorus were also measured. The phytoplankton community exhibited three main phases: During the first (02–15 April, chiefly surface biomass) and the second (20 April–10 May, deep biomass-maximum and spring bloom peak) periods, Phaeocystis pouchetii dominated biomass (ca. 50% of PPC) followed by vegetative cells of Chaetoceros socialis. In the third period (10 May onwards, characterized by surface estuarinecir-culation), dino- and microflagellates dominated the low post-bloom biomass. Protozooplankton comprising tintinnids, other ciliates and heterotrophic dinoflagellates increased in abundance. Vegetative cells of phytoplankton were scarce in trap collections at 50 m or below; resting cells of Chaetoceros comprised nearly all the intact sedimenting phytoplankton. Krill faeces accounted for >90% by volume of the total faecal material trapped, despite a >21 biomass dominance of copepods in the fjord. The greatest sedimentation rates of krill faeces were at > 100 m, reflecting the downward migration of krill during the day. In all, 2–3 g Cm^–2 of krill faeces were collected, representing ca. twice that from intact phytoplankton cells. POC in the traps at 50 m was ca. 11 gm^–2, accounting for ca. 17% of the estimated primary production during the study period. As the secondary production is high, a large proportion of the production of P. pouchetii must be grazed by herbivores. Copepod faeces are probably remineralized in the euphotic zone, while those of krill provide the major coupling between the pelagial and the benthos. The implications of such a sedimentation model for partitioning energy flow between the pelagial and the benthos is discussed.     

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.     

Some aspects of photosynthetic characteristics in a set of perennial irrigation reservoirs located in five river basins in Sri Lanka

Phytoplankton primary productivity of eleven irrigation reservoirs located in five river basins in Sri Lanka was determined on a single occasion together with light climate and nutrient concentrations. Although area-based gross primary productivity (1.43–11.65 g O₂ m^–2 d^–1) falls within the range already established for tropical water bodies, net daily rate was negative in three water bodies. Light-saturated optimum rates were found in water bodies, with relatively high algal biomass, but photosynthetic efficiency or specific rates were higher in water bodies with low algal biomass, indicating nutrient limitation or physiological adaptation of phytoplankton. Concentrations of micronutrients and algal biomass in the reservoirs are largely altered by high flushing rate resulting from irrigation release. Underwater light climate and nutrient availability control the rate of photosynthesis and subsequent area-based primary production to a great extent. However, morpho-edephic index or euphotic algal biomass in the most productive stratum of the water column is not a good predictor of photosynthetic capacity or daily rate of primary production of these shallow tropical irrigation reservoirs.     

Phycological studies in the North Channel,Lake Huron

The phytoplankton of North Channel in Lake Huron and its productivity was studied at 8 stations distributed across the channel during May to October, 1974. The phytoplankton analysis was conducted using the Utermohl technique. The mean percent biomass at each station indicated Diatomeae (59–77%) and phytoflagellates such as Chrysophyceae (4–21%) and Cryptophyceae (7–19%) as the dominant contributors. Seasonal variations of biomass ranged from 0.2 to 0.35 g·m^–3 with a single peak during stratified conditions. Diatomeae dominated throughout the period of investigation followed by Chrysophyceae and Cryptophyceae. Biomass composition by size revealed the dominance of ultraplankton (5–20 m) which contributed 29–68% to the total biomass. Species such as Fragilaria crotonensis, Tabellaria fenestrata, Synedra acus var. radians, Cyclotella comta and C. bodanica made substantial contributions during the unstratified and stratified conditions.Ultraplankton contributed overwhelmingly to the primary productivity as measured by carbon-14 uptake. The contaminant bioassays with single metals, metals in combination and a mixture of metals demonstrated that the ultraplankton's carbon assimilation was inhibited significantly, revealing their sensitivity to contaminants. Phytoplankton ecology of the Channel appears to be affected by tributary inflows, industrial/municipal inputs, and short flushing rates. However, statistical treatment of the ultraplankton biomass showed correlations with temperature and nutrients. Based on phycological and limnological characteristics, the Channel appears to be oligotrophic. The chlorophyll/biomass ratios and Activity Coefficient (P/B) align it with the most oligotrophic Lake Superior in its metabolic efficiency.     

Primary production and phytoplankton in two small,polyhumic forest lakes in southern Finland

Primary production and phytoplankton in polyhumic lakes showed a very distinct seasonal succession. A vigorous spring maximum produced by Chlamydomonas green algae at the beginning of the growing season and two summer maxima composed mainly of Mallomonas caudata Iwanoff were typical. The annual primary production was ca. 6 g org. C · m^–2 in both lakes. The mean epilimnetic biomass was 1.1 in the first lake and 2.2 g · m^–2 (ww) in the second one. The maximum phytoplankton biomass, 14 g · m^–2, was observed during the vernal peak in May.     

The productivity and carbon budget of a natural population of Daphnia lumholtzi Sars

D. lumholtzi in Lake Samsonvale, Queensland, Australia, is a small species (max. size approx. 7 µgC) that occurs in low abundance (max. abundance 6400 m^–3), with an average daily biomass of 3.32 mgC m^–3. Its annual rates of carbon assimilation, production and respiration, are 166, 110, and 56 mgC m^–3 y^–1 respectively. Annual biomass turnover (annual production/average daily biomass) is 33 and production efficiency is 50–66%. The population may consume 1.65–2.20 mgC m^–3 daily, equivalent to about 1% of the average daily standing crop of phytoplankton. Clutch size is small, 2 eggs, but represents 30–80% of a female's weight. A female may only produce 8–10 offspring in a full lifespan, nevertheless egg production may account for 56% of total production. The population shows autumn and spring peaks in abundance, and is believed to oversummer (4 months) as ephippia.     

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.     

Copepod grazing in a summer cyanobacteria bloom in the Gulf of Finland

Blooms of the cyanobacteria Nodularia spumigena and Aphanizomenon flos-aquae dominated the phytoplankton assemblages of the western Gulf of Finland and the eastern side of the northern Baltic Sea in late July–August, 1992. The bloom overlapped the peak seasonal contributions of the dominant mesozooplankton herbivores in the region, the copepods Acartia bifilosa and Eurytemora affinis and the cladoceran Bosmina longispina maritima. Using radio-labelling techniques; the copepods were offered one of the cyanobacteria, Nodularia, as well as the 10–54 µm fraction of the natural phytoplankton assemblage. In general, incorporation rates of the labelled phytoplankton into the copepods declined with increasing contributions of the cyanobacteria. For both copepods, incorporation was inversely related to total phytoplankton biomass, whether measured as chlorophyll, total cells or cyanobacteria biomass. The very low rates for Acartia (< 0.8 µl [copepod h]^–1) indicated that this copepod was likely starving in the cyanobacteria bloom, consistent with the generally poor condition of the animal observed in the laboratory. The other major mesozooplanktor, B. longispina maritima, ingested substantially more cyanobacterial biomass than the two copepods, based on HPLC-identified cyanobacteria-specific pigment echinenone in the gut. Bloom carbon provided < 1% and < 4% of the daily rations for Acartia and Eurytemora, respectively. Total copepod demand in the cyanobacteria blooms was trivial, < 1% of bloom biomass consumed daily. These results suggest that copepod herbivory is relatively unimportant in dissipating summer cyanobacteria blooms in the Gulf of Finland.     

Viral attack exacerbates the susceptibility of a bloom‐forming alga to ocean acidification

Both ocean acidification and viral infection bring about changes in marine phytoplankton physiological activities and community composition. However, little information is available on how the relationship between phytoplankton and viruses may be affected by ocean acidification and what impacts this might have on photosynthesis‐driven marine biological CO₂ pump. Here, we show that when the harmful bloom alga Phaeocystis globosa is infected with viruses under future ocean conditions, its photosynthetic performance further decreased and cells became more susceptible to stressful light levels, showing enhanced photoinhibition and reduced carbon fixation, up‐regulation of mitochondrial respiration and decreased virus burst size. Our results indicate that ocean acidification exacerbates the impacts of viral attack on P. globosa, which implies that, while ocean acidification directly influences marine primary producers, it may also affect them indirectly by altering their relationship with viruses. Therefore, viruses as a biotic stressor need to be invoked when considering the overall impacts of climate change on marine productivity and carbon sequestration.     

Seasonal variation in phytoplankton primary production in relation to light and nutrients in Lake Awasa,Ethiopia

The biomass and primary production of phytoplankton in Lake Awasa, Ethiopia was measured over a 14 month period, November 1983 to March 1985. The lake had a mean phytoplankton biomass of 34 mg chl a m^–3 (n = 14). The seasonal variation in phytoplankton biomass of the euphotic zone (mg chl a m^–2 h^–1) was muted with a CV (standard deviation/mean) of 31%. The vertical distribution of photosynthetic activity was of a typical pattern for phytoplankton with light inhibition on all but overcast days. The maximum specific rates of photosynthesis or photosynthetic capacity (Ø_max) for the lake approached 19 mg O₂ (mg chl a)^–1 h^–1, with high values during periods of low phytoplankton biomass. Areal rates of photosynthesis ranged between 0.30 to 0.73 g O₂ m^–2 h^–1 and 3.3 to 7.8 g O₂ m^–2 d^–1. The efficiency of utilisation of PhAR incident on the lake surface varied from 2.4 to 4.1 mmol E^–1 with the highest efficiency observed corresponding to the lowest surface radiation. Calculated on a caloric basis, the efficiency ranged between 1.7 and 2.9%. The temporal pattern of primary production by phytoplankton showed limited variability (CV = 21 %).     

Influence of gizzard shad on phytoplankton size and primary productivity in mesocosms and earthen ponds in the southeastern U.S.

Gizzard shad (Dorosoma cepedianum), a filter feeding omnivore, can consume phytoplankton, zooplankton and detritus and is a common prey fish in U.S. water bodies. Because of their feeding habits and abundance, shad have the potential to affect primary productivity (and hence water quality) directly through phytoplankton grazing and indirectly through zooplankton grazing and nutrient recycling. To test the ability of shad to influence primary productivity, we conducted a 16-day enclosure study (in 2.36-m³ mesocosms) and a 3-year whole-pond manipulation in 2–5 ha earthen ponds. In the mesocosm experiment, shad reduced zooplankton density and indirectly enhanced chlorophyll a concentration, primary productivity, and photosynthetic efficiency (assimilation number). While shad did not affect total phytoplankton density in the mesocosms, the density of large phytoplankton was directly reduced with shad. Results from the pond study were not consistent as predicted. There were few changes in the zooplankton and phytoplankton communities in ponds with versus ponds without gizzard shad. One apparent difference from systems in which previous work had been conducted was the presence of high densities of a potential competitor (i.e., larval bluegill) in our ponds. We suggest that the presence of these extremely high larval bluegill densities (20–350 larval bluegill m^–3; 3–700 times higher density than that of larval gizzard shad) led to the lack of differences between ponds with versus ponds without gizzard shad. That is, the influence of gizzard shad on zooplankton or phytoplankton was less than the influence of abundant bluegill larvae. Differences in systems across regions must be incorporated into our understanding of factors affecting trophic interactions in aquatic systems if we are to be able to manage these systems for both water quality and fisheries.     

The importance of grazing food chain for energy flow and production in three intertidal sand bottom communities of the northern Wadden Sea

In three intertidal sand bottom communities of the Königshafen (Island of Sylt, North Sea), the biomass production and respiration of phytobenthos, phytoplankton, macrozoobenthos, and in situ community metabolism were measured monthly during 1980. The study sites were characterized by different communities (Nereis-Corophium-belt, seagrass-bed,Arenicola-flat) and by a high abundance of the molluscHydrobia ulvae. Benthic diatoms are the major constituents of plant biomass in theArenicola-flat. In this community, gross primary productivity amounts to 148 g C m^–2 a^–1. 82 % of this productivity is caused by microbenthos, whereas phytoplankton constitutes only 18 %. In the seagrass-bed, gross primary productivity amounts to 473 g C m^–2 a^–1. 79 % of this is generated by seagrass and its epiphytes, whereas microphytobenthos contributes 19 %. In theNereis-Corophium-belt, only microphytobenthos is important for biomass and primary productivity (gross: 152 g C m^–2 a^–1). Annual production of macrofauna proved to be similar in theArenicola-flat (30 g C m^–2 a^–1) to that in the seagrass-bed (29 g C m^–2 a^–1). Only one third of this amount is produced in theNereis-Corophium-belt (10 g C m^–2 a^–1). The main part of secondary production and animal respiration is contributed by grazingH. ulvae. In the seagrass-bed, 83 % of the energy used for production is obtained from the grazing food chain. In theArenicola-flat and theNereis-Corophium-belt, the importance of non-grazing species is greater. A synchrony of seasonal development of plant biomass and monthly secondary production was observed. In theArenicola-flat and the seagrass-bed, where density and production of macrofauna are high, a conspicuous decrease in biomass of microbenthos occurs during the warmer season, whereas in theNereis-Corophium-belt primary production causes an increase in microphytobenthic biomass in summer and autumn. Energy flow through the macrofauna amounts to 69 g C m^–2 a^–1 in theArenicola-flat, 85 g C m^–2 a^–1 in the seagrass-bed and 35 g C m^–2 a^–1 in theNereis-Corophium-belt. Based on the assumption that sources of food are used in proportion to their availability, 49 g C m^–2 a^–1 (Arenicola-flat), 72 g C m^–2 a^–1 (seagrass-bed) and 26 g C m^–2 a^–1 (Nereis-Corophium-belt) are estimated as taken up by the grazing food chain. All three subsystems are able to support the energy requirements from their own primary production and are not dependent on energy import from adjacent ecosystems.     

The summer zooplankton community at South Georgia: biomass,vertical migration and grazing

Zooplankton abundance and biomass were determined during January 1990 at two stations to the north-west of South Georgia using a Longhurst Hardy Plankton Recorder (LHPR). At both shelf and oceanic station sites, zooplankton biomass, (excluding Euphausia superba), was found to be ca. 13 g dry mass m^–2. Copepods and small euphausiids dominated the catches. These estimates are over 4 times higher than values generally reported for the Southern Ocean and may reflect firstly, the high productivity of the study area, secondly, the time of year, summer, when biomass for many species is maximal, and thirdly, the high sampling efficiency of the LHPR. Principal components analysis disclosed similarities and differences between adjacent depth strata in terms of abundance, biomass and species composition. At both stations most variability occurred in the mixed layer (0–60 m) and thermocline (60–120 m) with depth horizons below this being more homogeneous. Diel migrations were observed for most taxa with abundance increasing in the mixed layer at night. At the oceanic station, species and higher taxa belonging to the mesopelagic community were generally well spread throughout this domain and, with the exception of Pleuromamma robusta and Metridia curticauda, showed little evidence of migration. The grazing impact of the epipelagic community (copepods and small euphausiids) was estimated to remove 3–4% of the microbial standing stock day^–1 and a conservative 25% and 56% of daily primary production at the oceanic and shelf stations respectively.     

High biomass and production of picoplankton in a Chinese integrated fish culture pond

The phytoplankton dynamics of a Chinese integrated fish culture pond in the suburbs of Shanghai were studied in September and October 1989. The chlorophyll a concentration was high with a range of 62.5–127.3 µg l^–1; however, daily net production of phytoplankton was relatively low, with a range of 0.53–1.94 gC m ^–2 d^–1. Of the total phytoplankton biomass, 70–87% was composed of nanoplankton (<10 µm) and picoplankton, probably because of the selective feeding by phytoplanktivorous carp. In particular, the chlorophyll a concentration of picoplankton was 2.1 – 14.1 mg m ^–3, and its contribution to total phytoplankton production rate was high (18–68%).     

Seasonal change in the proportion of bacterial and phytoplankton production along a salinity gradient in a shallow estuary

We intended to evaluate the relative contribution of primary production versus allochthonous carbon in the production of bacterial biomass in a mesotrophic estuary. Different spatial and temporal ranges were observed in the values of bacterioplankton biomass (31–273 g C l^–1) and production (0.1–16.0 g C l^–1 h^–1, 1.5–36.8 mg C m^–2 h^–1) as well as in phytoplankton abundance (50–1700 g C l^–1) and primary production (0.1–512.9 g C l^–1 h^–1, 1.5–512.9 mg C m^–2 h^–1). Bacterial specific growth rate (0.10–1.68 d^–1) during the year did not fluctuate as much as phytoplankton specific growth rate (0.02–0.74 d^–1). Along the salinity gradient and towards the inner estuary, bacterio- and phytoplankton biomass and production increased steadily both in the warm and cold seasons. The maximum geographical increase observed in these variables was 12 times more for the bacterial community and 8 times more for the phytoplankton community. The warm to cold season ratios of the biological variables varied geographically and according to these variables. The increase at the warm season achieved its maximum in the biomass production, particularly in the marine zone and at high tide (20 and 112 times higher in bacterial and phytoplankton production, respectively). The seasonal variation in specific growth rate was most noticeable in phytoplankton, with seasonal ratios of 3–26. The bacterial community of the marine zone responded positively – generating seasonal ratios of 1–13 in bacterial specific growth rate – to the strong warm season increment in phytoplankton growth rate in this zone. In the brackish water zone where even during the warm season allochthonous carbon accounted for 41% (on average) of the bacterial carbon demand, the seasonal ratio of bacterial specific growth rate varied from about 1 to 2. During the warm season, an average of 21% of the primary production was potentially sufficient to support the whole bacterial production. During the cold months, however, the total primary production would be either required or even insufficient to support bacterial production. The estuary turned then into a mostly heterotrophic system. However, the calculated annual production of biomass by bacterio- and phytoplankton in the whole ecosystem showed that auto- and heterotrophic production was balanced in this estuary.     

Biometry and trophodynamics of Salpa thompsoni foxton (Tunicata: Thaliacea) near the Antarctic Peninsula in austral summer, 1983–1984

Summary Salpa thompsoni aggregates have a biometric profile similar to that of mid-latitude salps, being approximately 96% water and only about 1% organic matter. Of its ash-free dry weight about 13.6% is carbon and 3.1% is nitrogen. All weight parameters were related to body length by a power function of 2.3. S. thompsoni was a dominant member of the zooplankton community in waters near the Antarctic Peninsula in the austral summer of 1983–1984, with biomass in mid-March ranging from 49 to 671 mgCm^–2 and 9.6 to 146 mgNm^–2. Three subpopulations occurred in separate regions: (1) the Bransfield Strait, (2) north of the South Shetland Islands, and (3) west of Elephant Island; these were dominated by 20, 30 and 40 mm individuals, respectively. Biomass was greatest in the Bransfield Strait and least near the South Shetland Islands. Clearance rate measurements of S. thompsoni on naturally occurring particulate matter were significantly lower than those previously reported for mid-latitude salps, a result which we attribute primarily to the effect of low habitat temperature (ca. 1°C). Direct measurements suggest that fecal production by 21 mm blastozoids is equivalent to 10.2% body carbon d^–1 and 6.6% body nitrogen d^–1. Grazing by S. thompsoni may have removed a majority of the daily primary production in March, but <1% in January. The comparatively low biomass of krill larvae in 1983–1984 may be attributed partially to competitive removal of food by salps, but an equally important effect may have been direct predation.     

The structure of the plankton community of the Öregrundsgrepen (southwest Bothnian Sea)

Taxonomic composition and variations in density and biomass of the plankton community in the Öregrundsgrepen, a shallow coastal area, were investigated from June 1972 to November 1973. The phytoplankton biomass was large in spring but small during the rest of the year. The spring bloom was dominated by diatoms and dinoflagellates, especially byThalassiosira spp. which were also important during other seasons. Small forms, such asCryptomonas spp.,Rhodomonas spp. and monads, dominated during summer. Blue-green algae were never of any major importance. During the summer, the trophogenic layer exceeded 10 m in thickness. The metazoan fauna was of lower diversity than the plankton flora. The dominating species, the copepodsAcartia bifilosa andEurytemora affinis, constituted on the average 83% of the standing crop. The low salinities, 5–6 S, were regarded as the principal pertinent limiting factor. The metazoan fauna reached large biomass values from July to October. The protozoan fauna (in the case of ciliates), obtained biomass maxima during the spring bloom. It is suggested that the Öregrundsgrepen represents an area of elevated productivity within a region of low overall production, presumably due to local upwelling. From June 1972 to May 1973, the average biomasses were: phytoplankton 0.464 g C m^–2, ciliates 0.040 g C m^–2, copepod nauplii 0.010 g C m^–2, micro-rotifers 0.004 g C m^–2, and mesozooplankton (larger than 0.2 mm) 0.312 g C m^–2. It is estimated that about than 60% of the phytoplankton production is consumed by the microzooplankton (<0.2 mm).