Vertical distribution of primary producers and zooplankton grazers during different phases of the Arctic spring bloom

During a circumnavigation of the Svalbard archipelago in May 2006, simultaneous marine environmental (meteorology, heat flux, ocean turbulence, irradiance) and biological (phytoplankton and zooplankton biomass/species) data were sampled at selected stations. The zooplankton data were supplemented by high-resolution, high-speed VPR sampling down to 100 m depth at most stations. We were able to sample different phases of the phytoplankton spring bloom in Arctic as well as in Atlantic waters, and the stations represented different situations with respect to irradiance, turbulence and water-column stability. Phytoplankton growth and depth distribution were physically controlled, while zooplankton distributions were affected by biological parameters and turbulence. Development of the zooplankton followed the phytoplankton bloom phase, which was progressing in a direction from west to east in the waters north of Svalbard, and southwards in the Barents Sea. Our results also showed that the zooplankton did not avoid Phaeocystis pouchetii colonies, which have earlier been described as toxic. Despite an early retreat of the ice this year there was no apparent mismatch between the phytoplankton bloom and the dominant mesozooplankton, Calanus spp.     

Early spring bloom phytoplankton-nutrient dynamics at the Celtic Sea Shelf Edge

Phytoplankton production was measured at the shelf edge region of the Celtic Sea in April/May 1994 at the beginning of the spring bloom. Size fractionated ¹⁴C uptake experiments showed that phytoplankton >2 μm dominated the bloom although, in the period immediately before the increase in phytoplankton biomass, picophytoplankton (<2 μm) was responsible for up to 42% of the production; in these late winter conditions, chlorophyll concentrations were generally <0.7 μg l^-1 and primary production was ca. 70 mmol C m^-2 d^-1. As the spring bloom developed, phytoplankton production rates of 120 mmol C m^-2 d^-1 were measured. Chlorophyll concentration increased to >2 μg l^-1 as a result of growth of larger phytoplankton, including diatoms, with large numbers of Nitzschia, Thalassionema and Chaetoceros dominating the assemblage. Picophytoplankton production declined as the spring bloom progressed. Nutrient concentrations were not depleted during the sampling period, and NO^-₃ concentrations were >6 μmol l^-1. Nutrient assimilation rates were measured at the same time as primary production was estimated. Before the development of any substantial phytoplankton biomass, the uptake rates for ammonium and nitrate were very similar, with f-ratios ranging from 0.5 to 0.6. Assimilation of ammonium remained relatively constant after the onset of stratification and bloom development, but nitrate uptake increased by a factor of 2 or more, resulting in f-ratios >0.8. There was significant phosphate uptake in the dark, which was generally ca. 50% of the rate in the light. The C : N : P assimilation ratios changed as the bloom developed; in the pre-bloom situation, when small phytoplankton cells dominated the assemblage, the C : N assimilation ratio was variable, with some stations having ratios less than (ca 2.5), and some higher than (ca. 9), the Redfield ratio. The most actively growing assemblages had N : P ratios close to the Redfield ratio, but the C : N ratios were consistently lower. New production was found to be closely correlated with the size of the species making up the phytoplankton assemblage, and high f ratios were measured when larger phytoplankton dominated the assemblage.     

Population dynamics of phytoplankton, heterotrophic bacteria, and viruses during the spring bloom in the western subarctic Pacific

We characterized the community composition of phytoplankton in the western subarctic Pacific from the pre-bloom to the decline phase of the spring bloom with special reference to decreases in the silicic acid concentration in surface waters as an index for diatom bloom development. Furthermore, responses of heterotrophic bacteria and viruses to the spring bloom were also concomitantly investigated. Under pre-bloom conditions when nutrients were abundant but the surface mixed layer depth was relatively deep, chlorophyll (Chl) a concentrations were consistently low and green algae (chlorophytes and prasinophytes), cryptophytes, and diatoms were predominant in the phytoplankton assemblages as estimated by algal pigment signatures. Together with the shallowing of the mixed layer depth and the decrease in silicic acid concentration, diatoms bloomed remarkably in the Oyashio region, though the magnitude of the bloom in the Kuroshio-Oyashio transition (hereafter Transition) region was relatively small. A total of 77 diatom species were identified, with the bloom-forming diatoms mainly consisting of Thalassiosira, Chaetoceros, and Fragilariopsis species. It has become evident that the carotenoid fucoxanthin can serve as a strong indicator of the diatom carbon biomass during the spring diatom bloom. Differences in the species richness of diatoms among stations generally enabled us to separate the Oyashio bloom stations from the Transition and the Oyashio pre-bloom stations. Relatively high values of the Shannon-Wiener index for the diatom species were also maintained during the Oyashio bloom, indicating that a wide variety of species then shared dominance. In the decline phase of the Oyashio bloom when surface nutrient concentrations decreased, senescent diatom cells increased, as inferred from the levels of chlorophyllide a. Although the cell density of heterotrophic bacteria changed little with the development of the diatom bloom, viral abundance increased toward the end of the bloom, suggesting an increased likelihood of mortality among organisms including diatoms resulting from viral infection. This is the first report on the microbial trophodynamics, including viruses, during the spring diatom bloom in the western subarctic Pacific.     

东亚边缘海区浮游植物春华的纬向与年际变化

Combined studies of latitudinal and interannual variations of annual phytoplankton bloom peak in East Asian marginal seas(17°–58°N, including the northern South China Sea(SCS), Kuroshio waters, the Sea of Japan and the Okhotsk Sea) are rarely. Based on satellite-retrieved ten-year(2003–2012) median timing of the annual Chlorophyll a concentration(Chl a) climax, here we report that this annual spring bloom peak generally delays from the SCS in January to the Okhotsk Sea in June at a rate of(21.20±2.86) km/d(decadal median±SD). Spring bloom is dominant feature of the phytoplankton annual cycle over these regions, except for the SCS which features winter bloom. The fluctuation of the annual peak timing is mainly within ±48 d departured from the decadal median peak date, therefore this period(the decadal median peak date ±48 d) is defined as annual spring bloom period. As sea surface temperature rises, earlier spring bloom peak timing but decreasing averaged Chl a biomass in the spring bloom period due to insufficient light is evident in the Okhotsk Sea from 2003 to 2012. For the rest of three study domains, there are no significant interannual variance trend of the peak timing and the averaged Chl a biomass. Furthermore this change of spring phytoplankton bloom timing and magnitude in the Okhotsk Sea challenges previous prediction that ocean warming would enhance algal productivity at high latitudes.     

Development of lipids during a spring plankton bloom in the northern North Sea: I. Particulate fatty acids

The plankton spring bloom in the northern North Sea was extensively investigated during a period of three months in 1976 at a fixed station occupied by the R.V. “Meteor”. Samples of different depth-profiles, representative of the phytoplankton development, were collected eleven times to analyze the concentration of fatty acids of the particulate matter. The water column was divided into an upper and lower layer according to the thermocline depths, because different processes take place in these layers. During the exponential growth phase the fatty acid concentration rose only slightly due to increases in polyunsaturated fatty acids (18:4, 20:5, 22:6), which are typical for marine plankton. With the exhaustion of nutrients the biochemical composition changed and the fatty acid concentration increased sharply from about 3 to 20 μmol C dm^? finally to about 30% of the particulate carbon. The main proportion consisted of oleic acid (28.3%) and palmitic acid (24.2%). The first phytoplankton bloom, dominated by diatoms (Chaetoceros species), was characterized by the increase in fatty acids with 16 carbon atoms, whereas during the second smaller bloom, with dinoflagellates as the main species, more fatty acids with 18 carbon atoms occurred. After the stationary growth phase the phytoplankton biomass strongly decreased, resulting in an increase of particulate matter below the thermocline. The fatty acid pattern there was similar to that during the stationary phase of the phytoplankton bloom in the upper layer.     

Physical controls and interannual variability of the Labrador Sea spring phytoplankton bloom in distinct regions

We investigated the variability of the spring phytoplankton bloom in the Labrador Sea, dividing into distinct biogeographical zones, then analyzing the relationship between the bloom and physical forcings. The spring phytoplankton bloom in the north Labrador Sea varied in intensity by a factor of 4 and in timing of onset by 3 weeks over the 11-year record from SeaWiFS satellite ocean chlorophyll, 1998–2008. This north bloom (north of 60 °N and west of the Labrador shelves) is earliest and most intense, owing in part to the offshore-directed freshwater stratification from the West Greenland Current. On interannual timescales, significant correlations were found between the north bloom intensity and ocean processes, namely offshore advection, eddy activity and runoff from Greenland. In contrast, the central Labrador Sea is later and weaker, and only a correlation between the bloom timing and irradiance was found. As the subpolar gyre shifts in strength and shape, freshwater outflow from the Arctic and Greenland changes, we may expect further changes in the biological response as indicated by these relationships.     

Effect of meteorological conditions on interannual variability in timing and magnitude of the spring bloom in the Irminger Basin,North Atlantic

Interannual variability in the spring bloom in the Irminger Basin, northern North Atlantic, is investigated using SeaWiFS-derived chlorophyll-a (chl-a) concentration and satellite or model-derived meteorological data. Variability in the timing and magnitude of the spring bloom in the basin is evaluated. A method for estimating a time series of Sverdrup's critical depth from satellite-derived data is introduced. Comparison with modelled mixed layer depth and chlorophyll concentration demonstrates that Sverdrup's critical depth model is valid for the Irminger Basin spring bloom. The dependence of the timing and magnitude of the spring bloom on winter pre-conditioning is investigated. We find that in the Irminger Basin the start of the spring bloom can be estimated from the preceding winter's mean wind speed and net heat flux. We also find that the maximum chl-a concentration during the bloom can be estimated from the frequency of winter storms. Increased storm activity results in a reduced bloom chlorophyll maximum by delaying the development of spring stratification, resulting in the bloom missing the ‘window of opportunity’ for optimum phytoplankton growth.     

The effects of horizontal advection on the spring bloom of phytoplankton in the central Southern Huanghai Sea

An algal bloom is defined as a relatively rapid increase in the biomass of phytoplankton in an aquatic system. During 30 March to 24 April 2007, a cruise was conducted in the central Southern Huanghai Sea to investigate the spring bloom processes. The spatial and temporal variations of phytoplankton are discussed based on the in-situ observations and simultaneous remote sensing data. The explosive algal blooming varied quickly in temporal and spatial scales, due to the highly patchy distribution. Data obtained at the 2 anchor stations (BM1 and BM2) were analyzed in the present study. Horizontal advection is speculated to be responsible for the abrupt decrease in the concentration of chlorophyll-a at stations BM1 and BM2. At station BM2, the intermediate high chlorophyll-a concentration, coinciding with the low temperature, was found to be advected from the inshore colder water mass located to the east of the site.     

Observations of sea ice interannual variations and spring bloom occurrences at the Japanese scallop farming area in the Okhotsk Sea using satellite imageries

The dynamics of ice formation and phytoplankton bloom development in the coastal region of the Okhotsk Sea, Hokkaido, where the Japanese scallop, Mizuhopecten yessoensis, are cultured were investigated using seven years (1998–2004) satellite data from the Special Sensor Microwave/Imager (SSM/I) and Sea-viewing Wide Field-of-view Sensor (SeaWiFS). The interannual variability of sea ice cover and timing of spring bloom occurrences were analyzed. Longer ice cover in 1999, 2001 and 2003 with the presence of ice until early April and shortened ice cover in 1998, 2000, 2002 and 2004 with the occurrence of ice until early March were recognized at this area. Variability in the timing of sea ice retreat and development of spring blooms at the scallop areas were observed. Progression of a single ice edge bloom showed higher Chl-a concentration compared to development of an initial ice edge bloom followed by a later open water bloom. Higher concentration of phytoplankton biomass was observed in the initial bloom when sea ice melting is delayed compared to when the sea ice leaves earlier. Wind events were also observed to affect the occurrences of spring bloom.     

The influence of lateral mixing on a phytoplankton bloom: Distribution in the Kerguelen Plateau region

A unique phytoplankton bloom appears every year during the austral spring/summer in the northern Kerguelen Plateau region. The Kerguelen Ocean and Plateau compared Study (KEOPS) showed that an increase in subsurface iron coming up from the seafloor through vertical mixing was responsible for the observed increase in chlorophyll-a above the plateau. We demonstrate that the bloom pattern is not a simple increase of biomass over shallow water: it is strongly influenced by the bathymetry and its spatial extent controlled by strong currents around the plateau. Here we focus on lateral mixing process to explain the particular shape of the bloom. We use the Smagorinsky [1963. General circulation experiments with the primitive equations. I. The basic experiment. Monthly Weather Review 91 (3), 99–164] formula to estimate and map fields of lateral mixing time scales (τ) due to barotropic tidal currents, barotropic atmospheric forced currents, Ekman velocities and geostrophic velocities. Results show that short time scale mixing is strongly influenced by the tides while the other processes have minor influences. Comparisons of τ and satellite chlorophyll-a images show that the spatial pattern of the bloom seems to be delimited by a barrier of high lateral mixing that is essentially due to tides. This emphasises the role played by the tides over the Kerguelen Plateau in supplying iron to the phytoplankton and containing the horizontal shape of the bloom. This is one of the first times such a link has been demonstrated, which has implications for the study of iron advection in the ocean.     

Top-down control of spring surface phytoplankton blooms by microzooplankton in the Central Yellow Sea,China

Phytoplankton growth and microzooplankton grazing were studied during the 2007 spring bloom in Central Yellow Sea. The surveyed stations were divided to pre-bloom phase (Chl a concentration less than 2 μg L⁻¹), and bloom phase (Chl a concentration greater than 2 μg L⁻¹). Shipboard dilution incubation experiments were carried out at 19 stations to determine the phytoplankton specific growth rates and the specific grazing rates of microzooplankton on phytoplankton. Diatoms dominated in the phytoplankton community in surface waters at most stations. For microzooplankton, Myrionecta rubra and tintinnids were dominant, and heterotrophic dinoflagellate was also important in the community. Phytoplankton-specific growth rates, with an average of 0.60±0.19 d⁻¹, were higher at pre-bloom stations (average 0.62±0.17 d⁻¹), and lower at the bloom stations (average 0.59±0.21 d⁻¹), but the difference of growth rates between bloom and pre-bloom stations was not statistically significant (t test, p=0.77). The phytoplankton mortality rate by microzooplankton grazing averaged 0.41±0.23 d⁻¹ at pre-bloom stations, and 0.58±0.31 d⁻¹ during the blooms. In contrast to the growth rates, the statistic difference of grazing rates between bloom and pre-bloom stations was significant (after removal of outliers, t test, p=0.04), indicating the importance of the top-down control in the phytoplankton bloom processes. Average potential grazing efficiency on primary productivity was 66% at pre-bloom stations and 98% at bloom stations, respectively. Based on our results, the biomass maximum phase (bloom phase) was not the maximum growth rate phase. Both phytoplankton specific growth rate and net growth rate were higher in the pre-bloom phase than during the bloom phase. Microzooplankton grazing mortality rate was positively correlated with phytoplankton growth rate during both phases, but growth and grazing were highly coupled during the booming phase. There was no correlation between phytoplankton growth rate and cell size during the blooms, but they were positive correlated during the pre-bloom phase. Our results indicate that microzooplankton grazing is an important process controlling the growth of phytoplankton in spring bloom period in the Central Yellow Sea, particularly in the “blooming” phase.     

Wind-dependent formation of phytoplankton spring bloom in Otsuchi Bay,a ria in Sanriku,Japan

Spring blooms of phytoplankton composed of centric diatoms developed in late February, March, and April in Otsuchi Bay on Sanriku ria coast, Japan. During this period, associated with prolonged seasonal west wind (>1 day), intense exchange of waters occurred between inside and outside the bay: outflow of nearsurface brackish water over inflow of oceanic water at depth. This circulation interrupted formation of the blooms, and transported phytoplankton populations seaward. By such water movements, a significant amount of nutrients in the bay was carried out, otherwise replenished into the bay, depending on water masses located outside the bay. Owing to irregular features of wind events, a bloom lasted from several days to a week. From February to April, supply of nutrients seemed to be replete except for the latter half of the bloom period, and estimates of the critical depth exceeded the depth of the bottom consistently. Thus, net growth of phytoplankton was expected throughout the observation period, and potentially blooms could be formed. However, the blooms were only formed under calm weather. We hypothesize that the exchange of waters dilutes populations in the bay, and that formation of the bloom, that is, accumulation of biomass depends on a balance between the growth of phytoplankton and the dilution of bay water.     

Variation of dissolved organic matter and fluorescence characteristics before,during and after phytoplankton bloom

The variation of dissolved organic matter (DOM) and fluorescence characteristics during the phytoplankton bloom were investigated in Yashima Bay, at the eastern part of the Seto Inland Sea, Japan. We found significant accumulations of dissolved organic carbon (DOC), dissolved organic nitrogen (DON), chromophoric dissolved organic matter (CDOM) fluorescence, and UV₂₆₀ during the phytoplankton bloom period in 2005, although lower accumulations of DOC and DON and only increases of CDOM fluorescence were observed during the bloom period in 2006. Little or no correlation between DOM and phytoplankton abundance might be due to the composition of DOM, which is a complex mixture of organic materials. The 3D-EEM results revealed that the DOM produced around the phytoplankton bloom period contained tyrosine, tryptophan, and humic-like substances. Our results showed that the occurrence of phytoplankton bloom contributed to the production of DOM in coastal water but the DOM accumulation depended on the type of phytoplankton bloom, the phytoplankton species in particular. From our results, we concluded that phytoplankton have a great role in the dynamics of DOM as a producer in a coastal environment.     

Carbon fluxes through major phytoplankton groups during the spring bloom and post-bloom in the Northwestern Mediterranean Sea

The carbon flux through major phytoplankton groups, defined by their pigment markers, was estimated in two contrasting conditions of the Northwestern Mediterranean open ocean ecosystem: the spring bloom and post-bloom situations (hereafter Bloom and Post-bloom, respectively). During Bloom, surface chlorophyll a (Chl a) concentration was higher and dominated by diatoms (53% of Chl a), while during Post-bloom Synechococcus (42%) and Prymnesiophyceae (29%) became dominant. The seawater dilution technique, coupled to high pressure liquid chromatography (HPLC) analysis of pigments and flow cytometry (FCM), was used to estimate growth and grazing rates of major phytoplankton groups in surface waters. Estimated growth rates were corrected for photoacclimation based on FCM-detected changes in red fluorescence per cell. Given the 30% average decrease in the pigment content per cell between the beginning and the end of the incubations, overlooking photoacclimation would have resulted in a 0.40 d^?1 underestimation of phytoplankton growth rates. Corrected average growth rates (μ_o) were 0.90±0.20 (SD) and 0.40±0.14 d^?1 for Bloom and Post-bloom phytoplankton, respectively. Diatoms, Cryptophyceae and Synechococcus were identified as fast-growing groups and Prymnesiophyceae and Prasinophyceae as slow-growing groups across Bloom and Post-bloom conditions. The higher growth rate during Bloom was due to dominance of phytoplankton groups with higher growth rates than those dominating in Post-bloom. Average grazing rates (m) were 0.58±0.20 d^?1 (SD) and 0.31±0.07 d^?1. The proportion of phytoplankton growth consumed by microzooplankton grazing (m/μ_o) tended to be lower in Bloom (0.69±0.34) than in Post-bloom (0.80±0.08). The intensity of nutrient limitation experienced by phytoplankton indicated by μ_o/μ_n (where μ_n is the nutrient-amended growth rate), was similar during Bloom (0.78) and Post-bloom (0.73). Primary production from surface water (PP) was estimated with ¹⁴C incubations. A combination of PP and Chl a synthesis rate yielded C/Chl a ratios of 34±21 and 168±75 (g:g) for Bloom and Post-bloom, respectively. Transformation of group-specific Chl a fluxes into carbon equivalents confirmed the dominant role of diatoms during Bloom and Synechococcus and Prymnesiophyceae during Post-bloom.     

Plankton community diversity from bacteria to copepods in bloom and non-bloom conditions in the Celtic Sea in spring

The plankton community composition comprising heterotrophic bacteria, pro-/eukaryotes, heterotrophic nanoflagellates, microzooplankton and mesozooplankton was assessed during the spring bloom and at non-bloom stations in the English Channel and Celtic Sea between 6 and 12 April 2002. Non-bloom sites were characterised by a dominance of pro-/eukaryotic phytoplankton <20 μm, higher abundance of heterotrophic nanoflagellates, microzooplankton standing stocks ranging between 60 and 380 mg C m⁻², lower mesozooplankton diversity and copepod abundance of between 760 and 2600 ind m⁻³. Within the bloom, the phytoplankton community was typically dominated by larger cells with low abundance of pro-/eukaryotes. Heterotrophic nanoflagellate cell bio-volume decreased leading to a reduction in biomass whereas microzooplankton biomass increased (360–1500 mg C m⁻²) due to an increase in cell bio-volume and copepod abundance ranged between 1400 and 3800 ind m⁻³. Mesozooplankton diversity increased with an increase in productivity. Relationships between the plankton community and environmental data were examined using multivariate statistics and these highlighted significant differences in the abiotic variables, the pro-/eukaryotic phytoplankton communities, heterotrophic nanoflagellate, microzooplankton and total zooplankton communities between the bloom and non-bloom sites. The variables which best described variation in the microzooplankton community were temperature and silicate. The spatial variation in zooplankton diversity was best explained by temperature. This study provides an insight into the changes that occur between trophic levels within the plankton in response to the spring bloom in this area.     

Physical controls and mesoscale variability in the Labrador Sea spring phytoplankton bloom observed by Seaglider

We investigated the 2005 spring phytoplankton bloom in the Labrador Sea using Seaglider, an autonomous underwater vehicle equipped with hydrographic, bio-optical and oxygen sensors. The Labrador Sea blooms in distinct phases, two of which were observed by Seaglider: the north bloom and the central Labrador Sea bloom. The dominant north bloom and subsequent zooplankton growth are enabled by the advection of low-salinity water from West Greenland in the strong and eddy-rich separation of the boundary current. The glider observed high fluorescence and oxygen supersaturation within haline-stratified eddy-like features; higher fluorescence was observed at the edges than centers of the eddies. In the central Labrador Sea, the bloom occurred in thermally stratified water. Two regions with elevated subsurface chlorophyll were also observed: a 5 m thin-layer in the southwest Labrador Current, and in the Labrador shelf-break front. The thin layer observations were consistent with vertical shearing of an initially thicker chlorophyll patch. Observations at the front showed high fluorescence down to 100 m depth and aligned with the isopycnals defining the front. The high-resolution Seaglider sampling across the entire Labrador Sea provides first estimates of the scale dependence of coincident biological and physical variables.     

Bottom-up control of phytoplankton growth in spring blooms in Central Yellow Sea,China

The source and significance of three nutrients – nitrogen, phosphorous and silicon – were investigated by a modified dilution method performed on seawater samples from the Central Yellow Sea (CYS), in spring blooming period of 2007. This modified dilution method accounted for the phytoplankton growth rate, microzooplankton grazing mortality rate, the internal and external nutrient pools, as well as nutrients supplied through remineralization by microzooplankton grazing. The results indicate that phytoplankton growth during the bloom is mostly contributed by internal nutrient pools (K_I=0.062–1.730). The external nutrient pools (K_E=<0–0.362) are also of importance for phytoplankton growth during the bloom at some sampling sites. Furthermore, the contribution of the recycled-nutrient pool by remineralization (K_R=<0–0.751) is significant when microzooplankton grazing rate was higher than 0.5 d⁻¹ during the spring phytoplankton blooms in the Central Yellow Sea. Compared with internal phosphorus, internal nitrogen and silicon contribute more to the phytoplankton production at most sampling stations.     

Arsenic,antimony and selenium speciation during a spring phytoplankton bloom in a closed experimental ecosystem

A study has been made of the effects of a spring diatom bloom on the levels and speciation of dissolved arsenic, antimony and selenium in the water enclosed in an experimental ecosystem moored in Loch Ewe (NW Scotland). Primary productivity resulted in severe depletion of phosphate and silicate in the bag, but had little effect on the levels and speciation of arsenic and antimony. Calculations based on phosphate depletion data strongly suggest that the field diatom population present during the experiment was capable of some degree of discrimination between phosphate and arsenate ions. Whilst biomethylation of arsenic was not observed in the upper region of the bag, where the phytoplankton population was at its greatest, the methylated form accounted for 64% of the dissolved arsenic at the base of the bag. In this region, however, the total dissolved arsenic levels were not higher than in the rest of the bag, suggesting microbial methylation of dissolved arsenic rather than the release of methylated arsenic from decaying phytoplankton.Total dissolved selenium and selenium(IV) showed some evidence of depletion during the development of the phytoplankton bloom, in support of previous observations of preferential selenite assimilation.     

Phytoplankton spring bloom of the Gironde plume waters in the Bay of Biscay: early phosphorus limitation and food-web consequences

During the spring 1995 (2–25 May), a cruise was carried on the RV Poseidon (Germany) on the continental shelf of the south Bay of Biscay. The objective was a comprehensive study of the planktonic food web within the Gironde plume waters. In these waters phosphate was present at very low concentrations (undetectable to < 0.1 μmol.L⁻¹), whereas nitrate, silicate and ammonium concentrations were much higher (several μmol·L⁻¹ for nitrate and silicate and 0.5 to 1.0 μmol·L⁻¹ for ammonium). The size distribution of the phytoplankton biomass (estimated from chlorophyll a measurements by high performance liquid chromatography) and primary production (measured by ¹⁴C in situ method) showed a great proportion of small (40 to 70 % < 3 μm) and active autotrophic cells (growth rates estimated from 0.4 to 0.8 d⁻¹ for the entire euphotic layer). Considering the very high values of NO₃-N:PO₄-P ratios and the high C:P and N:P ratios for the particulate organic matter, it is suggested that an early phosphorus depletion limits the spring bloom phytoplankton and particularly the new production (nitrate uptake coming from the Gironde waters).From these results and other simultaneous observations on the heterotrophic processes (such as grazing of microzooplankton), we can conclude that the planktonic food web would be close to a maintenance system as defined by Platt et al. The possible generalisation of these results for each spring is discussed with respect to the scarcity of previous and reliable phosphate data.     

Changes in structural and functional diversity of nematode communities during a spring phytoplankton bloom in the southern North Sea

The response of nematode communities to the sedimentation of a spring phytoplankton bloom in a sandy, well-oxygenated sediment at a single station (station 330) in the Southern North Sea was investigated monthly from early March to July 1999. Both structural (nematode density, diversity, vertical distribution and community composition) and functional (feeding type distributions, number of species within feeding groups) characteristics showed considerable changes shortly after the arrival of fresh organic material at the sediment surface. The general increase in numerical densities and diversity was related to changes within the groups of selective deposit-feeding and epistrate-feeding nematodes. It is hypothesised that sedimentation and subsequent remineralisation of fresh organic matter during the spring phytoplankton bloom result in an increase of suitable food items (both living and dead). This, combined with the availability of oxygen, creates conditions in which many nematode species can co-exist.