The biokinetic behavior of Tc in juvenile Coho Salmon, Oncorhynchus kisutch (Walbaum)

Juvenile coho salmon, Onchorynchus kisutch, were exposed to ^95mTc in both saltwater and freshwater to study the biokinetic behavior of this element in an anadromous fish. In freshwater, equilibrium whole-body concentration factors (CF₅) ranged from 28 to 32 in two separate experiments, in sharp contrast to an equilibriumCF of < 5 in saltwater. While the uptake kinetics were unimodal in saltwater, in freshwater, biomodal uptake kinetics were observed.Technetium-95m retention was biphasic in freshwater depuration experiments, an initial rapid loss of 21% to 26% of the steady-state activity with an elimination half-life of 3 to 5 days was followed by a slower loss rate, with a whole-body elimination half-life ranging from 23 to 33 days. In saltwater, retention was monophasic with an elimination half-life of 5–16 days. Dramatic decreases in ^95mTc body burdens when freshwater-labeled fish are transferred to Tc-labeled saltwater indicate that the changes in physiology accompanying saltwater acclimation lead to the loss of ^95mTc.     

Bioavailability of technetium from artificially labelled north-east atlantic deep-sea sediments

Laboratory experiments were designed to measure the uptake of Tc by clams from North-East Atlantic sediments which were contaminated with different oxidation states of ^95mTc. Distribution coefficients between solid sediment and pore water were similar for Tc IV and VII and never exceeded 3·5 during the 36-day experiment. Furthermore, ^95mTc was rapidly leached from the sediments with a half-time of about 4·5 days. Biological uptake was low, with transfer factors between clam tissues and sediment ranging between 0·04 and 0·6. Greater relative uptake was noted in the soft tissues than in shell, although the latter contained the largest fraction (70%) of the clam's whole body ^95mTc content. Contaminated clams, transferred to uncontaminated sediments, displayed a very long biological half-life (～120 days) for ^95mTc. This observation suggests that following acute contamination, clams living in an environment of this type would still retain Tc in their tissues long after the radionuclide had been leached from the sediments.     

Technetium: Uptake,organ distribution and loss in the mussel, Mytilus Californianus (Conrad) and the oyster Crassostrea gigas (Thunberg)

The bivalve molluscs Mytilus californianus and Crassostrea gigas were exposed to filtered seawater containing the isotope ^95mTc added as pertechnetate (TcO₄^?) to study the biokinetic behaviour of this element. Whole body concentration factors for both organisms at equilibrium were small (CF = 1·3–1·5); individual organ concentration factors were highest for the visceral mass in both. Loss rates determined both in the laboratory and under field conditions were biphasic for both molluscs; initial loss of Tc was rapid with slightly more than 50 % of the initial label being lost within 10 days. Thereafter, loss rates decreased and whole body biological half-lives ranged from 80 to 134 days. Neither I^? nor IO₃^? affected the uptake of Tc by M. californianus even when concentrations of these anions exceeded those normally present in seawater by two orders of magnitude.     

Cadmium bioconcentration in the echinoid Paracentrotus lividus: Influence of the cadmium concentration in seawater

Uptake and loss kinetics of cadmium were studied in Paracentrotus lividus exposed for 24 d to different stable Cd concentrations (0 to 1.14 μg Cd l⁻¹) and ¹⁰⁹Cd tracer added to seawater. The whole-body uptake kinetics were linear over the time course of the experiment. The whole-body ¹⁰⁹Cd concentration factor was independent of the stable Cd concentration in ambient seawater. Bioconcentration of Cd in whole individuals and their body compartments was directly proportional to the Cd concentration added to the seawater. The echinoid digestive tract wall showed the highest degree of Cd uptake. Whole-body loss kinetics were described by a 2-component exponential equation. The loss kinetics were similar for each of the treatments examined. Cadmium was found to display a long biological half-life in echinoid tissues; the major fraction (73 to 85%) of the Cd taken up by echinoids was eliminated following a loss component whose biological half-life was of the order of 1 year, regardless of the absolute Cd concentration accumulated by the echinoid. Paracentrotus lividus is suggested as a valuable biomonitor of Cd, particularly where knowledge of Cd concentration variations over long-term is of interest.     

Factors affecting the accumulation and elimination of silver (110mAg) in marine isopods

The bioaccumulation and elimination of silver-110 m was investigated in Idothea primastica. The retention of ^110mAg in the fecal pellets of Idothea was also investigated. The concentation factor was found to be relatively high (> 10³) at equilibrium and the bioaccumulation process was independent of temperature at 10°C and 20°C. It was also found that neither the loss rate from the animals nor the loss rate from fecal pellets were influenced by temperature. However, the loss rate from fecal pellets was significantly greater than that from whole animals. The retention half-times were found to be 130 days for the fecal pellets and 231 days for the animals. The loss rate of ^110mAg was higher in seawater than in brackish water.     

Factors affecting the biokinetics of technetium (95mTc) in marine macroalgae

Technetium (Tc) biokinetics were investigated in marine macroalgae using ^92mTc as tracer. Green and red algae accumulated Tc (VII) to a very low degree (CF ? 1–20); however, a much higher affinity for pertechnetate was found in some brown algal species (CF > 10³). Comparative tests with different species of brown algae revealed that technetium does not accumulate similarly in all species of this group. Moreover, no significant differences in radionuclide uptake were noted between brown algae exposed to Tc in either the IV or VII oxidation states. Bioaccumulation of technetium appears to be a metabolically controlled process since uptake did not occur in heat-killed individuals and both light and temperature significantly enhanced the accumulation of technetium in brown algae. Dissection of Sargassum vulgare following the uptake phase showed that the rapidly growing air bladder, leaf-like laterals and small branches contained higher Tc concentrations and retained a greater fraction of the radioactivity than the older, cylindrical main axis. Pertechnetate retention in two brown algae was found to be significantly different; their biological half-lives for Tc differed by an order of magnitude ($\text{T}{}_{\mathrm{<mtext>b</mtext><mtext>1</mtext><mtext>2</mtext>}}\text{= 19 and 196}\text{days}$). During depuration, loss took place more rapidly from the younger portions of the seaweed, as evidenced by the highest concentration and greatest fraction of Tc retained in the older, cylindrical main axis. Provided certain precautions are taken, brown algae such as Cystoseira compressa and S. vulgare would serve as good bioindicator organisms for the presence of Tc contamination in marine waters.     

Disposition and metabolism of 2,3,7,8-tetrachlorodibenzofuran (TCDF) in rainbow trout

In order to elucidate the metabolic fate of 2,3,7,8-tetrachlorodibenzofuran (TCDF) in fish and to thereby facilitate the assessment of the risks posed by this environmental toxin, we determined the whole body half-life, tissue distribution and metabolism of [³H TCDF in rainbow trout (Onchorynchus mykiss), treated orally. A whole body biphasic elimination pattern resulted in the excretion of 60% of the administered chemical during the first 3 days, after which a much slower elimination-rate (half-life = 14 days) was observed. Significant amounts of water-soluble metabolites were found in both bile and liver. Of the TCDF-derived radioactivity in bile, approximately 50% represented glucuronide conjugates, predominantly 4-hydroxy-2,3,7,8-TCDF: substantial amounts of the sulfate conjugate of this same metabolite were also present. Except at early time points, muscle contained the predominant fraction of TCDF-derived radioactivity, amounting to 25–65% of the total radioactivity present in the fish. More than 95% of the radioactivity present in muscle represented unmetabolized TCDF.     

The effects of salinity on uptake and metabolism of toluene and naphthalene by Dolly Varden,Salvelinus malma

Dolly Varden (Salvelinus malma) were force-fed ¹⁴C-toluene or ¹⁴C-naphthalene and held for 12, 24 and 48 h in freshwater or seawater (30%(.)) in order to determine the effect of salinity on uptake and metabolism of aromatic hydrocarbons. Fish held in seawater had slightly more ¹⁴C removed from the gut than did fish held in freshwater. Whether held in freshwater or seawater, toluene was more readily metabolized by fish than was naphthalene: after 48 h, 2–3 times more ¹⁴C from toluene was in the metabolite fraction of liver and central nervous system tissues. Fish held in seawater metabolized significantly less toluene and naphthalene than those in freshwater. The increased toxicity of toluene and naphthalene to Dolly Varden held in seawater appears to be the result of the decreased metabolism of these compounds by the fish.     

Biokinetics of selected heavy metals and radionuclides in two marine macrophytes: the seagrass Posidonia oceanica and the alga Caulerpa taxifolia

Uptake and loss kinetics of Zn, Ag, Cd, ¹³⁴Cs, and ²⁴¹Am by shoots of the seagrass Posidonia oceanica and fronds of the green alga Caulerpa taxifolia were determined in controlled laboratory radiotracer experiments using low contaminant concentrations. The two species accumulated most of the elements efficiently. The only exceptions were ¹³⁴Cs in both P. oceanica and C. taxifolia and Cd in C. Taxifolia (concentration factors 6.4). Steady state in uptake was reached in C. taxifolia for each element except Ag. In P. oceanica, steady state was noted for the uptake of Ag and ¹³⁴Cs whereas Zn, Cd, and ²⁴¹Am were linearly accumulated during the course of the experiment (15 d). With respect to relative metal bioavailability, the different compartments of P. oceanica shoots were generally ranked in the order: leaf epiphytes > adult LEAVES = intermediate leaves > leaf sheaths. The long-lived component of the loss kinetics for each element in P. oceanica was characterized by a relatively short biological half-life (T_b1/2 28 d). However, observations for the individual compartments indicated that adult leaves had a high retention capacity for Ag and ¹³⁴Cs, with virtually 100% retained after 21 d in uncontaminated sea water. In C. taxifolia, the long-lived component of the loss kinetics for each element was characterized by a T_b1/2 value that was not significantly different from infinity, an observation which suggests that a substantial fraction of the metal or radionuclide incorporated during a contamination event would be irreversibly bound by this algal species.     

An investigation into technetium binding in sediments

Coastal environments with reducing waters and/or sediments represent potential sinks for ⁹⁹Tc discharged to sea. Here, we have examined estuarine sediments from four geochemically distinct locations that have been exposed to ⁹⁹Tc discharged from Sellafield. Both the relative uptake and the operationally defined sediment “component” that holds the Tc were investigated in order to establish whether particular biogeochemical processes are predominately responsible for reducing and binding Tc in sediments. Despite the artefacts that can pose problems for sequential extractions, this scheme [Int. J. Environ. Anal. Chem. 51 (1993) 187] appears to be robust with regard to Tc. The results show that relative uptake of Tc varied greatly between the sites, with the highest occurring at an almost permanently anoxic fjord (Mariager Fjord, Denmark), followed by a brackish, seasonally eutrophic fjord (Roskilde Fjord, Denmark), then a sub-oxic salt marsh (which receives particle bound radionuclides from a more reducing mud patch; Esk Estuary, UK) and finally sulfidic and iron-reducing muddy sandy sediments (Needle's Eye, Solway Firth, Scotland). High relative uptake at the fjords was explained by the greater mixing of Tc-labelled oxic seawater into the part of the system where reduction of TcO₄⁻ was possible. Uptake at Mariager Fjord was higher than at Roskilde Fjord, reflecting the highly reducing geochemical conditions in the water body. Low uptake at Needle's Eye may be related to the speciation of technetium at this site as the sequential extraction data suggest that Tc is associated with the carbonate phase here. Tc carbonates are largely soluble, and this is the first observation of Tc association with carbonate fractions in the natural environment. The other three sites showed that organic matter, in conjunction with reducing conditions, was very important for binding and retaining Tc in sediments. The specific role of sulfides in controlling Tc retention in sediments was unclear because sulfides and organic matter are leached simultaneously in the sequential extraction scheme we applied, but there was evidence that Tc was not associated with acid-volatile iron monosulfides.     

Tissue distribution and kinetics of dissolved and nanoparticulate silver in Iceland scallop (Chlamys islandica)

The fast expansion of the global nanotechnology market entails a higher environmental and human exposure to nanomaterials. Silver nanoparticles (AgNP) are used for their antibacterial properties; however, their environmental fate is yet poorly understood. Iceland scallops (Chlamys islandica) were exposed for 12 h to three different silver forms, dissolved Ag(I) (Ag_diss), small (S-NP, ∅ = 10–20 nm) and large AgNP (L-NP, ∅ = 70–80 nm), labeled with ^110mAg, and bioaccumulation kinetics and tissue distribution using in vivo gamma counting and whole-body autoradiography were determined. All Ag forms were readily and rapidly accumulated. Elimination process was also fast and bi-exponential, with mean biological half-life ranging from 1.4 to 4.3 days and from 17 to 50 days for fast and slow compartments, respectively. Most of the radioactivity concentrated in the hepatopancreas. Ag_diss and S-NP tissue distributions were similar indicating a rapid dissolution of the latter in the tissues, contrarily to L-NP which appeared to form long lasting aggregates in the digestive system. Estimated steady-state bioconcentration factors (BCF), ranging between 2700 and 3800 ml g⁻¹ for dissolved and particulate silver forms, showed that C. islandica can accumulate significant quantities of Ag in a short time followed by an efficient depuration process.     

Nitrogen budget of the eelgrass, Zostera marina in a bay system on the south coast of Korea

Above- and below-ground productivities and tissue N content were measured monthly to quantify N incorporation to sustain eelgrass growth in Koje Bay on the south coast of Korea from January to December 2002. N acquisition was also estimated through measurements of N uptake kinetics, tissue biomass, and in situ inorganic N concentrations in water column and sediments. Above- and below-ground productivities were highest in summer and lowest in late fall and winter. Leaf tissue N content was highest in December and lowest in July, while rhizome tissue N content was highest in October and lowest in April. Estimated monthly N incorporation by leaf tissues based on the leaf productivity and N content ranged from 0.4 g N m^?2 month^?1 in November to 2.0 g N m^?2 month^?1 in May. N incorporation by below-ground tissues ranged from 0.1 g N m^?2 month^?1 in February to 0.2 g N m^?2 month^?1 in October. Annual whole plant N incorporation was 14.5 g N m^?2 y^?1, and N incorporation by leaf tissues accounted for about 87 % of total N incorporation. Maximum uptake rate (V _max ) and half saturation constant (K _m ) of leaf NH₄ ⁺ uptake were significantly lower than those of root NH₄ ⁺ uptake. Above- and below-ground biomass ranged from 20.8 g DW m^?2 and 8.6 g DW m^?2 in winter to 350.0 g DW m^?2 and 81.3 g DW m^?2 in spring, respectively. NH₄ ⁺ concentrations varied from 0.2 to 4.3 mM in water column and from 93.0 to 551.7 mM in sediment pore water. Based on these measurements, annual N acquisition by root tissues contributed slightly higher than that by leaf tissues to total plant N acquisition. During winter, monthly leaf N acquisition was lower than monthly leaf N incorporation. This implies that Z. marina has internal nitrogen retention system to offset the shortage and excess of nitrogen.     

Bioaccumulation et elimination du 65Zn par Gammarus aequicauda martimov

Uptake of ⁶⁵Zn by Gammarus aequicauda results in a concentration factor of approximately 50 and it is characterised by a maximal accumulation level attained as early as the third day of the experiment. After ingestion by the gammarids of twenty contaminated meals which are distributed over a 45-day period, a transfer of ⁶⁵Zn between the food and the consumer can be observed but there is no sign of the biomagnification phenomenon. The retention rate of the radionuclide is only about 1·5% and the ⁶⁵Zn concentration in the gammarids remains markedly inferior to that of the ingested food.The elimination of the ⁶⁵Zn fixed directly from water takes place according to an exponential model which corresponds to the existence of three biological half-lives of the radionuclide, $\text{Tb}{}_1\text{? 0·5 day, Tb}{}_2\text{? 3·5 days and Tb}{}_3\text{? days}$. The excretion of ⁶⁵Zn accumulated from food is a simple exponential phenomenon which corresponds to only one biological half-life of approximately 17 days.     

栉孔扇贝对无机砷的富集与排出特征研究

以栉孔扇贝(Chlamys,farreri)为试验生物,应用生物富集双箱动力学模型,研究了暴露在不同质量浓度的As<'3+>溶液中,栉孔扇贝对无机砷的耐受性;通过对富集与排出过程中栉孔扇贝体内无机砷含量的动态监测及对检测结果的非线性拟合,得出栉孔扇贝富集无机砷的吸收速率常数(k<,1>)、排出速率常数(k<,2>)、生...     

Cadmium accumulation,distribution and elimination in the bivalve Macoma balthica: Neither metallothionein nor metallothionein-like proteins are involved

Accumulation and elimination of cadmium was investigated in the tellinid clam, Macoma balthica (L.). Accumulation of Cd was linear in soft tissues (0·35 μg g⁻¹ day⁻¹ dry weight) throughout a 29-day exposure period at 100 μg Cd litre⁻¹. Loss of Cd, measured after transfer of experimentally-contaminated clams to clean seawater, was exponential and relatively slow (biological half-time, 70 days). In contrast, Cd uptake onto the shell of Macoma was characteristic of saturation kinetics, indicative of physical adsorption processes. Amounts of Cd accumulated by the shell were low, and the elimination rate rapid (half-time, 7 days) compared with soft tissues.Gel chromatographic profiles of cytosol extracts from control and experimental groups of M. balthica revealed that most of the Cd was bound to high molecular weight ligands, an unusual feature in bivalve molluscs. Although the proportion of cytosolic Cd associated with very low molecular weight ligands is small (< 15%) this pool may be important in regulating Cd fluxes in Macoma during uptake and elimination phases. No evidence was found of metallothionein (or similar metal-binding protein) involvement in Cd accumulation and storage in either field or laboratory exposed clams.The metabolism of Cd in M. balthica is different from that reported for other bivalve groups in several respects. In particular, the relatively slow rate of Cd accumulation in Macoma may be an important adaptive advantage for survival in contaminated areas and may compensate for the absence of a recognised detoxifying (MT) system in this species.     

Hydrodynamic modeling of flushing time in a small estuary of North Bay, Florida, USA

Freshwater fraction method is popular for cost-effective estimations of estuarine flushing time in response to freshwater inputs. However, due to the spatial variations of salinity, it is usually expensive to directly estimate the long-term freshwater fraction in the estuary from field observations. This paper presents the application of the 3D hydrodynamic model to estimate the distributions of salinity and thus the freshwater fractions for flushing time estimation. For a case study in a small estuary of the North Bay in Florida, USA, the hydrodynamic model was calibrated and verified using available field observations. Freshwater fractions in the estuary were determined by integrating freshwater fractions in model grids for the calculation of flushing time. The flushing time in the North Bay is calculated by the volume of freshwater fraction divided by the freshwater inflow, which is about 2.2 days under averaged flow conditions. Based on model simulations for a time series of freshwater inputs over a 2-year period, a power regression equation has been derived from model simulations to correlate estuarine flushing time to freshwater inputs. For freshwater input varying from 12 m³/s to 50 m³/s, flushing time in this small estuary of North Bay changes from 3.7 days to 1.8 days. In supporting estuarine management, the model can be used to examine the effects of upstream freshwater withdraw on estuarine salinity and flushing time.     

Mesozooplankton and ichthyoplankton distribution around Gran Canaria,an oceanic island in the NE Atlantic

In October 1991, mesozooplankton biomass and ichthyoplankton were studied in the waters surrounding the island of Gran Canaria (Canary Islands). The average dry weight obtained for mesozooplankton biomass (4.5 mg m⁻³) is typical of the area. Average fish egg abundance (94 eggs per 10 m²) was similar to that found previously for the Canary Current. However, the average fish larva abundance (904 individuals per 10 m²) was higher than previously recorded for the Canary Current and similar regions. The horizontal distributions of the planktonic components studied appear strongly related to the mesoscale oceanographic structures in the area. These included an area of weak flow around the stagnation point upstream of the island, where higher concentrations of neritic ichthyoplankton occurred, a warm lee region downstream, where mesozooplankton biomass and neritic ichthyoplankton were increased, particularly on the convergent anticyclonic boundary, and the offshore boundary of an upwelling filament from the NW African coast, which acted as a barrier for neritic ichthyoplankton. These concentrations suggest that the stagnation point and the lee are areas of retention for neritic fish eggs and larvae. Simple Lagrangian simulations of particle trajectories in the observed field of flow demonstrate the potential for retention of organisms, both passive and with limited swimming ability, in these areas. On the flanks of the island and in the filament, the simulation suggests even swimming organisms will be largely swept away. The various oceanographic structures, by increasing the planktonic production, are partially responsible for the relatively high values of abundance obtained for fish larvae.     

The effect of habitat and environmental history on otolith chemistry of barramundi Lates calcarifer in estuarine populations of a regulated tropical river

We examine the microchemistry of otoliths of cohorts of a fished population of the large catadromous fish, barramundi Lates calcarifer from the estuary of a large tropical river. Barramundi from the estuary of the large, heavily regulated Fitzroy River, north-eastern Australia were analysed by making transects of ⁸⁷Sr/⁸⁶Sr isotope and trace metal/Ca ratios from the core to the outer edge. Firstly, we examined the Sr/Ca, Ba/Ca, Mg/Ca and Mn/Ca and ⁸⁷Sr/⁸⁶Sr isotope ratios in otoliths of barramundi tagged in either freshwater or estuarine habitats that were caught by the commercial fishery in the estuary. We used ⁸⁷Sr/⁸⁶Sr isotope ratios to identify periods of freshwater residency and assess whether trace metal/Ca ratios varied between habitats. Only Sr/Ca consistently varied between known periods of estuarine or freshwater residency. The relationships between trace metal/Ca and river flow, salinity, temperature were examined in fish tagged and recaptured in the estuary. We found weak and inconsistent patterns in relationships between these variables in the majority of fish. These results suggest that both individual movement history within the estuary and the scale of environmental monitoring were reducing our ability to detect any patterns. Finally, we examined fish in the estuary from two dominant age cohorts (4 and 7 year old) before and after a large flood in 2003 to ascertain if the flood had enabled fish from freshwater habitats to migrate to the estuary. There was no difference in the proportion of fish in the estuary that had accessed freshwater after the flood. Instead, we found that larger individuals with of each age cohort were more likely to have spent a period in freshwater. This highlights the need to maintain freshwater flows in rivers. About half the fish examined had accessed freshwater habitats before capture. Of these, all had spent at least their first two months in marine salinity waters before entering freshwater and some did not enter freshwater until four years of age. This contrasts with the results of several previous studies in other parts of the range that found that access to freshwater swamps by larval barramundi was important for enhanced population productivity and recruitment.     

Nitroaromatic stimulation of superoxide production in three species of freshwater fish

Nitroaromatic compounds frequently contaminate aquatic systems and may, therefore, impact fish. However, a known pathway of nitroaromatic toxicity in mammals, that of nitroaromatic stimulated superoxide (O₂⁻) production, has yet to be addressed in fish. In this study we investigated this pathway in three species of freshwater fish-channel catfish (Ictalurus punctatus), largemouth bass (Micropterus salmoides) and rainbow trout (Salmo gairdneri)-exposed to nitrofurantoin (NF), p-nitrobenzoic acid (PNBA) and m-dinitrobenzene (MDNB). Our results indicate that these nitroaromatics elicit a stimulation of O₂⁻ production by fish liver fractions. Additionally, results suggests a similarity between, fish and mammals in the nitroreductases which mediate nitroaromatic activation and subsequent O₂⁻ production. These findings indicate a potential toxic consequence of fish exposure to nitroaromatic contaminants in aquatic systems.     

Primary production and nutrient assimilation in the Iberian upwelling in August 1998

Primary production was measured during two Lagrangian experiments in the Iberian upwelling. The first experiment, in a body of upwelled water, measured day-to-day changes in phytoplankton activity as the water mass moved south along the shelf break. Nutrient concentrations decreased over a five day period, with concomitant increases in phytoplankton biomass. Initially the maximum phytoplankton biomass was in the upper 10m but after four days, a sub-surface chlorophyll maximum was present at 30m. Depth-integrated primary production at the beginning of the experiment was 70mmolC.m⁻².d⁻¹ (838mgC.m⁻².d⁻¹) and reached a maximum of 88mmolC.m⁻².d⁻¹ (1053mgC.m⁻².d⁻¹) on day 3. On day 1, the picoplankton fraction (<2μm) was slightly more productive than larger (>5μm) phytoplankton, but the increase in overall production during the drift experiment was by these larger cells. Nitrate was the dominant nitrogen source. As nutrient concentrations declined, ammonium became increasingly more important as a nitrogen source and the f-ratio decreased from 0.7 to 0.5. Picoplankton cells (<2μm) were responsible for most (65–80%) of the ammonium uptake. The C:N:P uptake ratios were very close to the Redfield ratio for the first four days but as nutrients became depleted high C:N uptake ratios (11 to 43) were measured. Over the period of the experiment, nitrate concentration within the upper 40m decreased by 47.91mmolN.m⁻². In vitro estimates, based on ¹⁵N nitrate uptake, accounted for 56% of the decrease in nitrate concentration observed in the drifting water mass. Ammonium uptake over the same four day period was 16.28mmolN.m⁻², giving a total nitrogen uptake of 43.18mmolN.m⁻².In the second experiment, an offshore filament was the focus and a water mass was sampled as it moved offshore. Nutrient concentrations were very low (nitrate was <10nmol l⁻¹ and ammonium was 20–40nmol l⁻¹). Primary production rate varied between 36mmolC.m⁻².d⁻¹ (436mgC.m⁻².d⁻¹) and 21mmolC.m⁻².d⁻¹ (249mgC.m⁻².d⁻¹). Picophytoplankton was the most productive fraction and was responsible for a constant proportion (ca 0.65) of the total carbon fixation. Uptake rates of both nitrate and ammonium were between 10 and 20% of those measured in the upwelling region. Urea could be a very significant nitrogen source in these waters with much higher uptake rates than nitrate or ammonium; urea turnover times were ca. one day but the source of the urea remains unknown. Urea uptake had a profound effect on calculated f ratios. If only nitrate and ammonium uptake was considered, f ratios were calculated to be 0.42–0.46 but inclusion of urea uptake reduced the f ratio to <0.1. The primary production of this oligotrophic off-shore filament was driven by regenerated nitrogen.