An investigation into the occurrence and distribution of polycyclic aromatic hydrocarbons in two soil size fractions at a former industrial site in NE England,UK using in situ PFE–GC–MS

Polycyclic aromatic hydrocarbon (PAH) concentrations were determined in 16 topsoils (0–10 cm) collected across the site of a former tar works in NE England. The soils were prepared in the laboratory to two different particle size fractions: <250 μm (fraction A) and >250 μm to <2 mm (fraction B). Sixteen priority PAHs were analysed in the soils using in situ pressurised fluid extraction (PFE) followed by gas chromatography—mass spectrometry (GC–MS). The average total PAH concentration in the soils ranged from 9.0 to 1,404 mg/kg (soil fraction A) and from 6.6 to 872 mg/kg (soil fraction B). These concentrations are high compared with other industrially contaminated soils reported in the international literature, indicating that the tar works warrants further investigation/remediation. A predominance of higher-molecular-weight compounds was determined in the samples, suggesting that the PAHs were of pyrogenic (anthropogenic) origin. Statistical comparison (t-test) of the mean total PAH concentrations in soil fractions A and B indicated that there was a significant difference (95% confidence interval) between the fractions in all but two of the soil samples. Additionally, comparisons of the distributions of individual PAHs (i.e. 16 PAHs × 16 soil samples) in soil fractions A and B demonstrated generally higher PAH concentrations in fraction A (i.e. 65.8% of all individual PAH concentrations were higher in soil fraction A). This is important because fraction A corresponds to the particle size thought to be most important in terms of human contact with soils and potential threats to human health.     

Arsenic distribution and bioaccessibility across particle fractions in historically contaminated soils

Incidental soil ingestion is a common contaminant exposure pathway for humans, notably children. It is widely accepted that the inclusion of total soil metal concentrations greatly overestimates the risk through soil ingestion for people due to contaminant bioavailability constraints. The assumption also assumes that the contaminant distribution and the bioaccessible fraction is consistent across all particle sizes. In this study, we investigated the distribution of arsenic across five particle size fractions as well as arsenic bioaccessibility in the <250-, <100-, <10- and 2.5-μm soil particle fractions in 50 contaminated soils. The distribution of arsenic was generally uniform across the larger particle size fractions but increased markedly in the <2.5-μm soil particle fraction. The marked increase in arsenic concentration in the <2.5-μm fraction was associated with a marked increase in the iron content. Arsenic bioaccessibility, in contrast, increased with decreasing particle size. The mean arsenic bioaccessibility increased from 25 ± 16% in the <250-μm soil particle fraction to 42 ± 23% in the <10-μm soil particle fraction. These results indicate that the assumption of static arsenic bioaccessibility values across particle size fractions should be reconsidered if the ingested material is enriched with small particle fractions such as those found in household dust.     

Sediment geochemistry and arsenic mobilization in shallow aquifers of the Datong basin,northern China

Understanding the mechanism of arsenic (As) mobilization from sediments to groundwater is important for water quality management in areas of endemic arsenic poisoning, such as the Datong basin in northern China. The bulk geochemistry analysis of sediment samples from three 50-m boreholes drilled specifically for this study at As-contaminated aquifers, the groundwaters of which have an As concentration up to 1060 μg/l, revealed that the average bulk concentrations of major and trace elements of the samples are similar to those of the average upper continental crust. The average As content of the sediment samples (18.7 mg/kg) is higher than that of modern unconsolidated sediments (5–10 mg/kg). Moreover, the abundance of elements varied with grain size, with higher concentrations in finer fractions of the sediments, such as silt and clay. The concentration of NH₂OH–HCl-extracted iron (Fe) strongly correlated with that of extracted As, suggesting that Fe oxyhydroxides may be the major sink of As in the aquifer. The results of microcosm experiments showed that As mobilization from sediments to groundwater is probably mainly related to changes in the redox conditions, with moderately reducing conditions being favorable for As release from sediments into groundwater.     

Feeding of Clausocalanids (Calanoida,Copepoda) on naturally occurring particles in the northern Gulf of Aqaba (Red Sea)

A total of 12 feeding experiments were conducted in the northern Gulf of Aqaba during spring (March/April) and autumn (September/October) 2002 at the Marine Science Station (MSS) in Aqaba. Females of three species of clausocalanids were selected: Clausocalanus farrani, C. furcatus and Ctenocalanus vanus. Natural occurring particle (NOP) larger than 5 μm were investigated as food source. The ambient chlorophyll a concentration at sampling depth (∼70 m) ranged between 0.15 and 1.00 μg chl a l⁻¹ and NOP concentrations ranged between 1.78 and 14.0 × 10³ cells l⁻¹ during the sampling periods. The division of particles into five size classes (5–10, 10–20, 20–50, 50–100 and >100 μm) revealed that most of the particles were found in the size classes below 50 μm (81–98%), while most of the natural occurring carbon (NOC) was concentrated in the size classes larger than 20 μm (70–95%). Ingestion rates were food density dependent rather than size dependent ranging between 0.02 and 1.65 × 10³ NOP ind⁻¹ day⁻¹ and 0.01 and 0.41 μg NOC ind⁻¹ day⁻¹, respectively, equivalent to a body carbon (BC) uptake between 0.4 and 51.8% BC day⁻¹. The share of the size classes to the total ingestion resembled in most cases the size class composition of the natural particle community.     

Lead speciation in indoor dust: a case study to assess old paint contribution in a Canadian urban house

Residents in older homes may experience increased lead (Pb) exposures due to release of lead from interior paints manufactured in past decades, especially pre-1960s. The objective of the study was to determine the speciation of Pb in settled dust from an urban home built during WWII. X-ray absorption near-edge structure (XANES) and micro-X-ray diffraction (XRD) analyses were performed on samples of paint (380–2,920 mg Pb kg⁻¹) and dust (200–1,000 mg Pb kg⁻¹) collected prior to renovation. All dust samples exhibited a Pb XANES signature similar to that of Pb found in paint. Bulk XANES and micro-XRD identified Pb species commonly found as white paint pigments (Pb oxide, Pb sulfate, and Pb carbonate) as well as rutile, a titanium-based pigment, in the <150 μm house dust samples. In the dust fraction <36 μm, half of the Pb was associated with the Fe-oxyhydroxides, suggesting additional contribution of outdoor sources to Pb in the finer dust. These results confirm that old paints still contribute to Pb in the settled dust for this 65-year-old home. The Pb speciation also provided a clearer understanding of the Pb bioaccessibility: Pb carbonate > Pb oxide > Pb sulfate. This study underscores the importance of taking precautions to minimize exposures to Pb in house dust, especially in homes where old paint is exposed due to renovations or deterioration of painted surfaces.     

Transferral of HMs pollution from road-deposited sediments to stormwater runoff during transport processes

Ratio of turbidity and TSS (Tur/TSS) was used to characterize PSD of stormwater particles. Pb and Zn preferred to accumulate in finer RDS, while Cu, Cr and Ni in coarser RDS. HMs pollution in stormwater particles increased linearly with Tur/TSS. Dissolvability of HMs and PSD variations contribute to the differences between RDS and stormwater. Stormwater runoff, derived from the wash-off of road-deposited sediments (RDS), contains elevated heavy metal (HM) concentrations and, thus, imposes an increasing threat to urban aquatic ecosystems. In-depth understanding of the variations of HMs pollution from RDS to stormwater during transport processes facilitates the development of effective RDS and stormwater control strategies. Toward this end, the distribution of HMs (Cu, Pb, Zn, Cr, and Ni) in RDS and stormwater were investigated simultaneously. The results show a preferential accumulation of Pb and Zn in the finer (<38.5 μm) RDS, and Cu, Cr and Ni in the coarser (38.5–150 μm) RDS. For stormwater, n.d.~48.6% of HMs fractionated into the dissolved phase, and stormwater particles constitute the primary carriers of HMs. Furthermore, the accumulation of HMs in stormwater particles increased linearly with finer particle size distributions (PSD). Geoaccumulation index (I_geo) highlighted the predominant pollution of both RDS and stormwater particles by Cu, Pb and Zn. Nonetheless, Cu, Pb, and Ni mostly contributed the potential ecological risk of RDS, whereas Cu, Pb, and Zn mainly contributed that of stormwater particles. Moreover, contamination by Cu, Pb and Zn was significantly higher in stormwater particles than that in RDS. These differences are attributable to the solubility and size-dependent accumulation of HMs in RDS, as well as the PSD variations during transport processes. The study outcomes highlight the importance of very fine (nano- and submicron- scale) RDS in stormwater pollution and the necessity of control.     

Vehicle-related ammonia emissions in Hong Kong

Weekly passive sampling of ambient ammonia has been performed at ground or rooftop levels at 12 locations in Hong Kong representing different land use categories. The highest weekly average roadside level of ammonia in Hong Kong was 7.1 μg m⁻³ at a street canyon site. Ambient ammonia concentrations for a rooftop urban-residential site with nearby light traffic were <1 μg m⁻³, being less than at an adjacent road and indoor car-park. Rooftop levels of ammonia showed a significant correlation with nitrogen monoxide concentrations. Honeycomb denuder samplings were also carried out at the rooftop site and the results were consistent with passive sampling. It is concluded that the 0.54 M vehicles in Hong Kong make a considerable contribution to ambient ammonia concentrations, which are otherwise low.     

Radionuclides,trace elements,and radium residence in phosphogypsum of Jordan

Voluminous stockpiles of phosphogypsum (PG) generated during the wet process production of phosphoric acid are stored at many sites around the world and pose problems for their safe storage, disposal, or utilization. A major concern is the elevated concentration of long-lived ²²⁶Ra (half-life = 1,600 years) inherited from the processed phosphate rock. Knowledge of the abundance and mode-of-occurrence of radium (Ra) in PG is critical for accurate prediction of Ra leachability and radon (Rn) emanation, and for prediction of radiation-exposure pathways to workers and to the public. The mean (±SD) of ²²⁶Ra concentrations in ten samples of Jordan PG is 601 ± 98 Bq/kg, which falls near the midrange of values reported for PG samples collected worldwide. Jordan PG generally shows no analytically significant enrichment (<10%) of ²²⁶Ra in the finer (<53 μm) grain size fraction. Phosphogypsum samples collected from two industrial sites with different sources of phosphate rock feedstock show consistent differences in concentration of ²²⁶Ra and rare earth elements, and also consistent trends of enrichment in these elements with increasing age of PG. Water-insoluble residues from Jordan PG constitute <10% of PG mass but contain 30–65% of the ²²⁶Ra. ²²⁶Ra correlates closely with Ba in the water-insoluble residues. Uniformly tiny (<10 μm) grains of barite (barium sulfate) observed with scanning electron microscopy have crystal morphologies that indicate their formation during the wet process. Barite is a well-documented and efficient scavenger of Ra from solution and is also very insoluble in water and mineral acids. Radium-bearing barite in PG influences the environmental mobility of radium and the radiation-exposure pathways near PG stockpiles.     

Water-soluble inorganic ions in airborne particulates from the nano to coarse mode: a case study of aerosol episodes in southern region of Taiwan

In 2004, airborne particulate matter (PM) was collected for several aerosol episodes occurring in the southern region of Taiwan. The particulate samples were taken using both a MOUDI (Micro-orifice Uniform Deposit Impactor) and a nano-MOUDI sampler. These particulate samples were analyzed for major water-soluble ionic species with an emphasis to characterize the mass concentrations and distributions of these ions in the ambient ultrafine (PM_0.1, diameter <0.1 μm) and nano mode (PM_nano, diameter <0.056 μm) particles. Particles collected at the sampling site (the Da-Liao station) on the whole exhibited a typical tri-modal size distribution on mass concentration. The mass concentration ratios of PM_nano/PM_2.5, PM_0.1/PM_2.5, and PM₁/PM_2.5 on average were 1.8, 2.9, and 71.0%, respectively. The peak mass concentration appeared in the submicron particle mode (0.1 μm < diameter <1.0 μm). Mass fractions (percentages) of the three major water-soluble ions (nitrate, sulfate, and ammonium) as a group in PM_nano, PM_0.1, PM₁, and PM_2.5 were 18.4, 21.7, 50.0, and 50.7%, respectively. Overall, results from this study supported the notion that secondary aerosols played a significant role in the formation of ambient submicron particulates (PM_0.1−1). Particles smaller than 0.1 μm were essentially basic, whereas those greater than 2.5 μm were neutral or slightly acidic. The neutralization ratio (NR) was close to unity for airborne particles with diameters ranging from 0.18 to 1 μm. The NRs of these airborne particles were found strongly correlated with their sizes, at least for samples taken during the aerosol episodes under study. Insofar as this study is exploratory in nature, as only a small number of particulate samples were used, there appears to be a need for further research into the chemical composition, source contribution, and formation of the nano and ultrafine mode airborne particulates.     

Chemical speciation and bioaccessibility of lead in surface soil and house dust,Lavrion urban area,Attiki, Hellas

In the Lavrion urban area study, Hellas, a five-step sequential extraction method was applied on samples of ‘soil’ (n = 224), affected by long-term mining and metallurgical activities, and house dust (n = 127), for the purpose of studying the potential bioaccessibility of lead and other metals to humans. In this paper, the Pb concentrations in soil and house dust samples are discussed, together with those in rocks and children’s blood. Lead is mainly associated with the carbonate, Fe–Mn oxides and residual fractions in soil and house dust. Considering the very low pH of gastric fluids (1–3), a high amount of metals, present in soil (810–152,000 mg/kg Pb) and house dust (418–18,600 mg/kg Pb), could be potentially bioaccessible. Consequently, children in the neighbourhoods with a large amount of metallurgical processing wastes have high blood-Pb concentrations (5.98–60.49 μg/100 ml; median 17.83 μg/100 ml; n = 235). It is concluded that the Lavrion urban and sub-urban environment is extremely hazardous to human health, and the Hellenic State authorities should urgently tackle this health-related hazard in order to improve the living conditions of local residents.     

Heavy metals in potable groundwater of mining-affected river catchments,northwestern Romania

Groundwater, accessed using wells and municipal springs, represents the major source of potable water for the human population outside of major urban areas in northwestern Romania, a region with a long history of metal mining and metallurgy. The magnitude and spatial distribution of metal contamination in private-supply groundwater was investigated in four mining-affected river catchments in Maramureş and Satu Mare Counties through the collection of 144 groundwater samples. Bedrock geology, pH and Eh were found to be important controls on the solubility of metals in groundwater. Peak metal concentrations were found to occur in the Lapuş catchment, where metal levels exceed Dutch target and intervention values in up to 49% and 14% of samples, respectively. A 700 m wide corridor in the Lapuş catchment on either side of the main river channel was identified in which peak Cd (31 μg l⁻¹), Cu (50 μg l⁻¹), Pb (50 μg l⁻¹) and Zn (3,000 μg l⁻¹) concentrations were found to occur. Given the generally similar bedrock geologies, lower metal levels in other catchments are believed to reflect differences in the magnitude of metal loading to the local environment from both metal mining and other industrial and municipal sources. Sampling of groundwater in northwestern Romania has indicated areas of potential concern for human health, where heavy metal concentrations exceed accepted environmental quality guidelines. The presence of elevated metal levels in groundwater also has implications for the implementation of the EU Water Framework Directive (WFD) and achieving ‘good’ status for groundwater in this part of the Danube River Basin District (RBD).     

Spatial distribution,pollution level,and health risk of Pb in the finer dust of residential areas: a case study of Xi'an,northwest China

Environmental Geochemistry and Health - The spatial distribution, pollution level, and exposure risk of Pb in the finer dust (particle size?&lt;?63&nbsp;μm) of residential...     

Size fractionation and characterization of nanocolloidal particles in soils

A protocol was developed to fractionate soil particles down to the nanocolloid scale by combining sieving, sedimentation, centrifugation, and cross-flow filtration (CFF). The validity of the method and the performance of the CFF system were tested by characterizing fractions using laser granulometry, electron microscopy, and chemical analysis. The 0.1-μm-pore-size membrane CFF system effectively retained nanocolloids (<0.1 μm) as shown by laser granulometry and observed directly by transmission electron microscopy. However, environmental scanning electron microscopy images of freeze-dried colloids were very different from their TEM counterparts, suggesting that sample preparation influenced microscopy imaging. Chemical analysis of Cu, Cd, and organic carbon in each fraction showed that the concentrations of these components increased as particle size decreased, indicating colloids and nanocolloids play an important role in retaining trace metals. Particle-size fractionation combined with chemical analysis and electron microscopy can provide insight into the nature and properties of nanocolloids in soil.     

Scope for growth of Mytilus?galloprovincialis (Lmk., 1819) in oligotrophic coastal waters (Southern Tyrrhenian Sea, Italy)

The ‘scope for growth’ (SFG) tool was used to study the growth performance of cultivated populations of Mytilus galloprovincialis (Lmk., 1819) in an oligotrophic area of the Southern Mediterranean Sea. The study was carried out between 1993 and 1996 by using data from four seasonal oceanographic cruises and from growth experiments. Water samples were collected and analysed for total suspended matter (TSM), particulate organic carbon (POC) and nitrogen (PON), particulate lipids, proteins and carbohydrates and chloropigments. The sum of the carbon equivalents of carbohydrates, proteins and lipids is indicated as the total biopolymeric particulate organic carbon (BPC) and was converted into a unit of energy in order to calculate the SFG of a theoretical mussel of 5 cm length. In order to test the performance of mussel growth at two depths (5 and 15 m water depth), mussel body size [as ash free dry weight (AFDW)] and the actual concentrations of BPC were used to calculate the monthly SFG using the physiological energetic relationships suggested in the current literature. Data from the field cruises led us to characterise the study site as ultra-oligotrophic (annual average of chloropigment concentration approximately 0.5 μg L⁻¹). SFG calculations allowed us to identify a site where mussels grown successively were found to reach a commercial size in approximately 12 months. The good agreement obtained between energetic response and subsequent production response suggests that the available energy from particulate food could be fully available for organic production for maintaining “proportionate” growth trajectories, even in a ultra-oligotrophic system.     

Pigment composition and size distribution of phytoplankton in a confined Mediterranean salt marsh ecosystem

Pigment composition and size distribution of phytoplankton were analysed in a group of Mediterranean salt marshes, where hydrology is dominated by sudden inputs during sea storms, followed by long periods of confinement. These marshes are characterized by a low inorganic–organic nutrient ratio, and inorganic nitrogen is especially scarce due to denitrification. Nutrients were the main factor affecting phytoplankton biomass, while zooplankton grazing did not control either phytoplankton community composition, or their size distribution. The relative abundance of the different phytoplankton groups was analysed by correspondence analysis using the pigment composition measured by high-performance liquid chromatography (HPLC) and analysed with the CHEMTAX programme. In this analysis, phytoplankton pigment composition was correlated with two nutrient gradients. The first gradient was the ratio of nitrate–total nitrogen (TN), since the different phytoplankton groups were distributed according to their eco–physiological differences in nitrogen uptake. The second gradient was correlated with total nutrient loading. Biomass size distributions frequently showed a lack of intermediate sized nanophytoplankton (2.5–4 μm in diameter), and the importance of this lack of intermediate sizes correlated with dinoflagellate biomass. These results suggested that in confined environments, where nutrients are mainly in an organic form, dinoflagellates take advantage of their mixotrophy, by competing and grazing on smaller phytoplankters simultaneously.     

Scope for growth of <Emphasis Type="Italic">Mytilus galloprovincialis</Emphasis> (Lmk., 1819) in oligotrophic coastal waters (Southern Tyrrhenian Sea,Italy)

The ‘scope for growth’ (SFG) tool was used to study the growth performance of cultivated populations of Mytilus galloprovincialis (Lmk., 1819) in an oligotrophic area of the Southern Mediterranean Sea. The study was carried out between 1993 and 1996 by using data from four seasonal oceanographic cruises and from growth experiments. Water samples were collected and analysed for total suspended matter (TSM), particulate organic carbon (POC) and nitrogen (PON), particulate lipids, proteins and carbohydrates and chloropigments. The sum of the carbon equivalents of carbohydrates, proteins and lipids is indicated as the total biopolymeric particulate organic carbon (BPC) and was converted into a unit of energy in order to calculate the SFG of a theoretical mussel of 5 cm length. In order to test the performance of mussel growth at two depths (5 and 15 m water depth), mussel body size [as ash free dry weight (AFDW)] and the actual concentrations of BPC were used to calculate the monthly SFG using the physiological energetic relationships suggested in the current literature. Data from the field cruises led us to characterise the study site as ultra-oligotrophic (annual average of chloropigment concentration approximately 0.5 μg L⁻¹). SFG calculations allowed us to identify a site where mussels grown successively were found to reach a commercial size in approximately 12 months. The good agreement obtained between energetic response and subsequent production response suggests that the available energy from particulate food could be fully available for organic production for maintaining “proportionate” growth trajectories, even in a ultra-oligotrophic system.     

Adsorptive separation of phosphate oxyanion from aqueous solution using an inorganic adsorbent

Phosphate removal from aqueous solution was explored using granular ferric hydroxide (GFH) as an inorganic adsorbent. Adsorption, desorption and kinetic studies were conducted on laboratory scale to evaluate the performance of GFH as an adsorbent for low concentrations of phosphate solution. The effect of pH on adsorption was investigated, and phosphate uptake was shown to decrease with an increase in solution pH, with maximum removal seen to occur at pH 3. The experimental data best fit the Temkin isotherm at both pH 3 and 4. Uptake of phosphate by GFH follows second-order kinetics, with the small particle range (76–200 μm) removing phosphate from the solution more rapidly than the larger particle range (710–850 μm). The kinetic results suggest that intra-particle diffusion is an important factor in phosphate adsorption onto GFH. Thermodynamic parameters (ΔG°, ΔH°, ΔS°) were evaluated, and the results indicated that the adsorption process was endothermic and spontaneous. This study demonstrates that GFH has potential to be used as a cost-effective adsorbent for phosphate removal from aqueous solution.     

Groundwater vulnerability to selenium in semi-arid environments: Amman Zarqa Basin,Jordan

An evaluation of ~250 samples of groundwater in the Amman Zarqa Basin for selenium along with other major and trace elements showed that concentrations of Se ranged between 0.09 and 742 μg/L, with an average value of about 24 μg/L. Selenium concentrations exceeded the recommended threshold for drinking water of the World Health Organization (WHO; 10 μ/L of Se) in 114 samples, with greater than 50 μg/L (quantity equivalent to the Jordanian standard of the allowed concentration of the element in water) of Se in nine cases. The average concentrations of Se in the lower, middle, and upper aquifers of the basin were 3.41, 32.99, and 9.19 μg/L, respectively. Based on the correlation with geologic formations and the statistical analysis of major/minor constituents and Piper tri-linear diagrams, we suggest that carbonate/phosphate dissolution, oxidation–reduction processes, and fertilizers/irrigation return flow are, together, the primary factors affecting the chemistry of the groundwater. Factor analysis helped to define the relative role of limestone-dolomitic dissolution in the aquifers (calcium, magnesium, and bicarbonate), agricultural activities (sulfate, nitrates, phosphorus, and potassium), oxidation–reduction factor (Eh, Fe, Mn, Cu, Zn, and Se), and anthropogenic (industrial) factor (EC, Fe, Cr, Co, Zn, and As). The high variability in Se concentrations might be related to the possibility of a multi-source origin of Se in the area.     

Determination of the swimming trajectory and speed of chain-forming dinoflagellate <Emphasis Type="Italic">Cochlodinium polykrikoides</Emphasis> with digital holographic particle tracking velocimetry

The marine dinoflagellate Cochlodinium polykrikoides is a harmful and highly motile algal species. To distinguish between the motility characteristics of solitary and chain-forming cells, the swimming trajectories and speeds of solitary cells and 2- to 8-cell chains of C. polykrikoides were measured using a digital holographic particle tracking velocimetry (PTV) technique. C. polykrikoides cells exhibited helical swimming trajectories similar to other dinoflagellate species. The swimming speed increased as the number of cells in the chain increased, from an average of 391 μm s⁻¹ (solitary cells) to 856 μm s⁻¹ (8-cell chain). The helix radius R and pitch P also increased as the number of cells in the chain increased. R increased from 9.24 μm (solitary cell) to 20.3 μm (8-cell chain) and P increased from 107 μm (solitary cell) to 164 μm (8-cell chain). The free thrust-generating motion of the transverse flagella and large drag reduction in the chain-forming cells seemed to increase the swimming speed compared to solitary cells. The measured swimming speeds agreed with those from field observations. The superior motility of chain-forming C. polykrikoides cells may be an important factor for its bloom, in addition to the factors reported previously.     

Change in the concentrations of iron in different size fractions during growth of the oceanic diatom Chaetoceros sp.: importance of small colloidal iron

 Laboratory culture experiments were performed to study the changes in size-fractionated Fe concentrations during the growth of the oceanic diatom Chaetoceros sp. Fe concentration was estimated for three size fractions: large labile particles (>0.2 μm), small colloidal particles (0.2 μm to 200 kDa) and soluble species (<200 kDa). The size-fractionated Fe concentration in the nutrient-enriched filtered seawater medium without diatom cells became stable within 4 d after the spike of FeCl₃ solution. Light irradiation by white fluorescent tubes with a 14 h light:10 h dark cycle did not significantly alter concentrations of the size-fractionated Fe. For the phytoplankton culture experiment, Fe-starved diatom cells were inoculated into the nutrient-enriched media aged for 19 d after the addition of FeCl₃. With the growth of diatom cells, total acid-labile Fe concentrations decreased from 0.60 to 0.46 nM during 7 d of incubation. However, only the concentration of the small colloidal particles showed a significant decrease; the concentration of the other size fractions remained relatively constant. Although the media still contained sufficient amounts Fe as large labile particles and soluble species, diatom cells appeared to be Fe-limited once Fe as small colloidal particles had been used up. These results suggest that Fe in the small colloidal particle fraction was the most dynamic size fraction during the growth of the diatom Chaetoceros sp. In addition, to better understand Fe dynamics in the ocean, we must consider the influence of phytoplankton growth on small colloidal Fe [which is typically included in the dissolved Fe fraction (<0.2 μm)]. Received: 9 December 1999 / Accepted: 5 May 2000