Suspended Particulate Matter Samples Research Articles

Distribution and sources of aliphatic and polycyclic aromatic hydrocarbons in suspended particulate matter in water from two Brazilian estuarine systems

The levels of selected organic markers, including 17 polycyclic aromatic hydrocarbons (PAHs), 16 of which are classified as priority pollutants by the US-EPA and perylene, aliphatic hydrocarbons (total and linear alkanes) and petroleum biomarkers (hopanes and steranes), were measured in suspended particulate matter (SPM) of the Mundaú–Manguaba estuarine-lagoon system (MMELS) in northeastern Brazil and the Paraíba do Sul River (PSR) estuary in southeastern Brazil, both of which are affected by sugarcane agriculture and urbanization. A total of 33 surface water samples of SPM were collected (22 from the MMELS and 11 from the PSR). The ∑16PAH ranged from 221 to 1243 ng g −1 in the MMELS and from 228 to 1814 ng g −1 in the PSR. Hopane and sterane concentrations in the PSR were higher than in the MMELS due to the input from petrogenic sources in PSR. The contributions of higher plants were also observed by n-alkane analyses. The PAH isomeric ratios indicated that the SPM from MMELS showed characteristics of combustion from biomass or petroleum and PSR was associated to petrogenic input, either from combustion or from unburned petroleum. Three sampling sites located near to the sugarcane plant and mouth of the rivers showed higher PAH concentrations and may largely be considered as highly contaminated. However, levels of n-alkanes and petroleum biomarkers in both study areas were relatively low.

Assessment of the sources of suspended particulate matter aerosol using US EPA PMF 3.0

The main purpose of this paper was to carry out a source apportionment of suspended particulate matter (SPM) samples using positive matrix factorization procedure. The central and local Government of Japan introduced strict emission regulations in 2002/10 and 2003/10, respectively, in curbing SPM pollution from major metropolitans. This paper also highlighted the impact of the measures taken by the central and local Government of Japan on the reduction of SPM and the contributions of sources. SPM samples were collected for 6 years starting from 1999 to 2005 at two sites, i.e., site A (urban) and site B (suburban) of Yokohama, Japan. Microwave digestion and inductively coupled plasma-mass spectroscopy (ICP-MS) were employed to measure Mg, Al, Ca, V, Cr, Mn, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Ag, Cd, Cs, Ba, Pb and Bi, while water soluble ions (Na(+), NH₄⁺, K(+), Ca(2+), Mg(2+), Cl(-), NO₃⁻ and SO₄²⁻ as well as carbonaceous mass (EC and OC) were analyzed using ion chromatograph and CHN analyzer, respectively. The sources identified at two sites were automobile, soil dust, marine aerosol, mixed sources, and secondarily formed aerosol. Also, source quantification was performed. Automobile and soil dust were striking contributors at site A. Automobile and soil dust of SPM aerosol might be produced from local origin at current study areas. Besides, Asian dust had an impact on high concentrations of SPM aerosol in some certain period of the year due to the outflows of East Asian emission. In contrast, secondary aerosol in the form of sulfate and ammonium as well as mixed sources (coal, long-transported Cs, and other unknown sources) were remarkable at site B. Stationary/industrial combustion has apparently more impact on the release of SPM components at site B than A. Automobile regulations in 2002 and 2003, respectively, resulted in reduction of SPM by 28% for site A and 16% for site B. There was also net reduction of automobile contribution at both sites due to the above measures being implemented.

Quantifying uncertainty in the measurement of arsenic in suspended particulate matter by Atomic Absorption Spectrometry with hydride generator

Arsenic is the toxic element, which creates several problems in human being specially when inhaled through air. So the accurate and precise measurement of arsenic in suspended particulate matter (SPM) is of prime importance as it gives information about the level of toxicity in the environment, and preventive measures could be taken in the effective areas. Quality assurance is equally important in the measurement of arsenic in SPM samples before making any decision. The quality and reliability of the data of such volatile elements depends upon the measurement of uncertainty of each step involved from sampling to analysis. The analytical results quantifying uncertainty gives a measure of the confidence level of the concerned laboratory. So the main objective of this study was to determine arsenic content in SPM samples with uncertainty budget and to find out various potential sources of uncertainty, which affects the results. Keeping these facts, we have selected seven diverse sites of Delhi (National Capital of India) for quantification of arsenic content in SPM samples with uncertainty budget following sampling by HVS to analysis by Atomic Absorption Spectrometer-Hydride Generator (AAS-HG). In the measurement of arsenic in SPM samples so many steps are involved from sampling to final result and we have considered various potential sources of uncertainties. The calculation of uncertainty is based on ISO/IEC17025: 2005 document and EURACHEM guideline. It has been found that the final results mostly depend on the uncertainty in measurement mainly due to repeatability, final volume prepared for analysis, weighing balance and sampling by HVS. After the analysis of data of seven diverse sites of Delhi, it has been concluded that during the period from 31st Jan. 2008 to 7th Feb. 2008 the arsenic concentration varies from 1.44 ± 0.25 to 5.58 ± 0.55 ng/m3 with 95% confidence level (k = 2).

Optimization and development of analytical methods for the determination of new brominated flame retardants and polybrominated diphenyl ethers in sediments and suspended particulate matter

With more stringent legislation on brominated flame retardants, it is expected that increasing amounts of substitutes would replace polybrominated diphenylethers (PBDEs). Therefore, the development and optimization of analytical methodologies that allow their identification and quantification are of paramount relevance. This work describes the optimization of an analytical procedure to determine pentabromochlorocyclohexane, tetrabromo-o-chlorotoluene, 2,3,5,6-tetrabromo-p-xylene, tetrabromophthalic anhydride, 2,3,4,5,6-pentabromotoluene, tris(2,3-dibromopropyl)phosphate, decabromodiphenylethane and 1,2-bis(2,4,6-tribromophenoxy)ethane together with PBDEs in sediments and in suspended particulate matter. This method comprises a pressurized liquid extraction followed by three cleanup steps (gel permeation chromatography and solid phase extraction on Oasis™ HLB and on silica cartridges). Gas chromatography–mass spectrometry, using electron capture negative chemical ionization, is used for the final analysis. The proposed method provides recoveries >85%. The method was applied to sediment and suspended particulate matter samples from different locations in the Western Scheldt estuary (the Netherlands). To the best of our knowledge, this is the first time that the occurrence of the additive flame retardants 2,3,5,6-tetrabromo-p-xylene, 3,4,5,6-tetrabromo-o-chlorotoluene and 2,3,4,5,6-pentabromochlorocyclohexane is reported in the literature. The concentrations of these new flame retardants ranged from 0.05 to 0.30 μg/kg dry weight.Electronic supplementary materialThe online version of this article (doi:10.1007/s00216-011-4807-8) contains supplementary material, which is available to authorized users.

Salinity control on long-chain alkenone distributions in lake surface waters and sediments of the northern Qinghai-Tibetan Plateau, China

Long-chain alkenones in lacustrine settings are potentially excellent biomarkers for the reconstruction of past terrestrial environmental conditions, and have been found in many different types of lakes around the globe. A wider range of factors influence the occurrence and distribution of alkenones in lake sediments and waters when compared to marine systems. Lake environmental conditions, such as temperature (in particular) and salinity, are among the key factors controlling alkenone distributions in lacustrine settings. Here we investigated alkenone distribution patterns in lakes of the northern Qinghai-Tibetan Plateau, China, and their possible relationship with environmental conditions, by analyzing paired samples of suspended particulate matter in surface waters and surface sediments. Salinity of investigated lake waters ranges from almost 0 to ∼100 g/L, while temperature variation among the lakes is minimal, effectively eliminating temperature effects on the alkenone distribution patterns observed here. We show that (1) alkenone concentrations vary substantially between the lakes, yet controlling mechanisms remain elusive; (2) C 37/C 38 ratios are substantially lower in the lakes of the Qaidam Basin than in the Lake Qinghai region, probably indicating different alkenone producers in the two regions; and (3) large variations in %C 37:4 (the percentage of the C 37:4 alkenone), determined from both surface waters and sediments, are negatively correlated with salinity. We suggest that the %C 37:4 index could be used as a salinity indicator at least on a regional scale, with careful considerations of other potentially complicating factors. However, potential reasons for why salinity could significantly affect %C 37:4 values need further investigation.

Heavy Metals Distribution in Suspended Particulate Matter and Sediment Collected from Vlora Bay (Albania): A Methodological Approach for Metal Pollution Evaluation

Heavy metals (Al, Fe, As, Cd, Cr, Cu, Hg, Mn, Ni, Pb, Zn) content was evaluated in suspended particulate matter and sediment samples collected from Vlora Bay (Albania) in the framework of Centro Internazionale di Scienze del Mare (CISM) Project activities. The trend of the metals (in general, overlapping that showed by the suspended particulate matter distribution), together with the linear correlation values found between metals, suggested the pivotal role of the Vjosa River and of the inner circulation scheme of Vlora Bay on their distribution. The geoaccumulation index, Igeo, was calculated as a criterion to assess if a metal concentration found in the sediment represents contamination level or can be considered as background level. The results show that metals concentrations in sediments can be considered near the background levels found in the Mediterranean Sea, even if some accumulation was found in several stations. The data were compared to Sediment Quality Guidelines considering the ERL (effects range low) and ERM (effects range medium) values, to evaluate the potential effects of sediment-associated metals on aquatic organisms. The Ni value for all samples was above the ERM value, while Cr and As values were in between ERL and ERM. Metal speciation was also evaluated in some sediment samples. Generally, the metals found were associated with the refractory phases, which constitute up to 80% of the total concentration. Moreover, the sampling strategies and the adopted analytical methods were compared to those recommended by national and international regulations.

Natural, anthropogenic and fossil organic matter in river sediments and suspended particulate matter: A multi-molecular marker approach

Different classes of organic matter (OM) have been systematically investigated in sediments and suspended particulate matter (SPM) along the Danube River in order to understand causes of compositional changes. Analytical pyrolysis revealed the dominance of natural organic matter (NOM) in most of the samples. The predominance of aquatic biomass is evident mainly from the abundance of organonitrogen compounds and phenol distributions. As the river enters a forested gorge, the terrestrial component of the NOM in sediments is more significant. This is reflected in abundant methoxyphenols and a very high carbon preference index. SPM sample from a tributary shows a unique geochemical signature. It contains abundant carboxylic acids, amines, isoprenoids in the pyrolyzate, and is dominated by phytol and 24-methyl-cholesta-5,24(28)-dien-3β-ol in the extract, produced by a diatom bloom. Wax esters with a relatively high proportion of short, methyl-branched alkyl-chains appear together with abundant phytadienes and n-C 17 alkane in some samples, suggesting a microbial origin. Anthropogenic OM from runoff and atmospheric deposition was evident from a minor input of polycyclic aromatic hydrocarbons (PAHs) originating from mixed combustion sources. Multivariate analysis using PAH data led us to define simple molecular ratios to distinguish the PAH composition in sand and silty sediments. The newly defined ratios are the alkylated phenanthrenes and anthracenes ratio (APA; C 1-C 3/C 0–C 3 phenanthrenes and anthracenes) and the PAH ring number ratio (RN; 5–6 ring parent PAHs/all parent PAHs). This demonstrates that alkylated, as well as 5–6 ring PAHs are better preserved in the finer than in coarser grained sediments. A ubiquitous, but minor input of petroleum-related contamination with a uniform composition was evident in all samples as revealed by the analysis of petroleum biomarkers. This study demonstrates that the investigation of different classes of riverine OM requires a detailed molecular analysis, applying a series of analytical techniques and adequate statistical data treatment.

Comparative studies of chemical composition of particulate matter between sea and remote location of eastern part of India

Suspended particulate matter (SPM) was collected by using high volume samplers (HVS) from two different locations: Bay of Bengal (BoB) and State Botanical Garden (SBG) situated in the eastern part of India. The SPM samples were collected on Whatman No.41 filter papers. The samples were simultaneously collected daily from both the locations during March 17–April 1, 2006. The average SPM concentration over BoB and SBG was found to be 39.05 and 78.14 μg/m 3 respectively. Na + and SO 4 2− were the most dominant water-soluble constituents over BoB and SBG respectively. The ratio of SO 4 2−/NO 3 − concentrations in both the cases was observed to be > 1 indicating that the contribution of atmospheric acidity was more due to SO 4 2− than NO 3 −. From intra-correlation analysis it is found that at both the locations, Na + and Cl − were well correlated while SO 4 2−-Ca 2+ and SO 4 2−-NH 4 + were poorly correlated indicating the later ion pairs to be derived from different sources. The Windrose diagrams for wind speed and direction show that for SBG, the wind blew from the SE and SW directions and brought in pollutants from soil and anthropogenic sources. In case of BoB, the wind parcels mostly were blown from the land mass (EES direction) showing the influence of anthropogenic pollutants on the marine aerosols. All the variables can be classified into three factors using principal component analyses technique. It explained 85% of total variance.

Seasonal Variation in the Mineralogy of the Suspended Particulate Matter of the Lower Changjiang River at Nanjing, China

AbstractThe source and temporal changes of minerals transported by the world's large rivers are important. In particular, clay minerals are important in evaluating the maturity of suspended sediments, weathering intensity, and source area. To examine seasonal changes in mineralogical compositions of the Changjiang River (CR), suspended particulate matter (SPM) samples were collected monthly for two hydrological cycles in Nanjing city and then were studied using X-ray diffraction (XRD), diffuse reflectance spectrophotometry (DRS), X-ray fluorescence spectrometry (XRF), and chemical analyses. The results indicate that the concentration of CR SPM ranges from 11.3 to 152 mg/L and is highly correlated to the rate of water discharge, with a greater concentration in flood season and lower concentrations during the dry season. CaO, MgO, and Na2O increase with increasing discharge whereas Al2O3 decreases sharply with increasing discharge. Dolomite, calcite, and plagioclase show strikingly similar seasonal variations and increase with increasing discharge with maximum concentrations in the flood season. In contrast, the clay mineral content exhibits the opposite trend with the lowest concentrations in the flood season. Illite dominates the clay minerals of the CR SPM, followed by chlorite, kaolinite, and smectite. Illite and kaolinite show distinctly seasonal variations; SPM contains more illite and less kaolinite during the flood season than during the dry season. The illite chemistry index and crystallinity, as well as kaolinite/illite ratio, all indicate intense physical erosion in the CR basin during the rainy season. Total iron (FeT) and highly reactive iron (FeHR) concentrations display slight seasonal changes with the smallest values observed during the flood season. Goethite is the dominant Fe oxide mineral phase in the CR SPM and hematite is a minor component, as revealed by DRS analyses. The FeT flux and FeHR flux are 2.786×106 T/y and 1.196×106 T/y, respectively.

Polycyclic aromatic hydrocarbons in effluents from wastewater treatment plants and receiving streams in Tianjin, China

Surface water, suspended particulate matter, pore water, and sediment samples were collected and analyzed for polycyclic aromatic hydrocarbons (PAHs) in Yongding New River, South Drainage Canal and North Drainage Canal, which receive most of wastewater from industrial city of Tianjin. PAH concentrations in effluent samples of wastewater treatment plants (WTP) discharging into the South Drainage Canal and North Drainage Canal were quantified for the first time. The results showed that the discharge of the WTPs recently only contributed to the PAH contamination in the canals near the outlets of the WTPs. PAH levels in sediments of the streams were greatly higher than those in soils by riverbank probably due to receiving large amounts of untreated wastewater. Unusually high benz[a] anthracene concentration strongly influenced the seasonal and spatial variation of total PAH concentrations in South Drainage Canal. Paired samples t test of ∑Nap, Fl, Phe, Fluo and ∑Nap, Phe, Fluo, Chry concentrations, which were dominant components in the air samples from non-heating and heating season, respectively, in the suspended particulate matters from the streams showed that PAH source from air deposition was more important for Yongding New River than that for South Drainage Canal and North Drainage Canal. Source apportionment based on PAH profiles indicated that coal combustion was the major PAH contamination source, and coke oven sources and wood combustion also contributed to the PAH contamination of the streams. This was further indicated by organic petrography analysis.

Distribution patterns of nitroaromatic compounds in the water, suspended particle and sediment of the river in a long-term industrial zone (China)

Nitroaromatic compounds are known to be hazardous to ecological and human health. To assess the status of nitroaromatic compounds contamination in the main rivers in the important industrial bases of the northeastern China, we collected water, suspended particulate matter (SPM) and sediment samples from 28 sites in the Daliao River watershed and analysed them for eight nitroaromatic compounds by gas chromatography. The total concentrations of eight nitrobenzenes in the water column including aqueous and SPM phases ranged from 740 to 15,828 ng L( - 1), with a mean concentration of 3,460 ng L( - 1). The total concentrations of eight nitrobenzenes in the sediment were 7.47 to 8,185.76 ng g( - 1), with a mean concentration of 921.98 ng g( - 1), and several times higher than those found from the Yellow River in China. 4-Nitrotoluene was the predominant contaminant in the water and sediment of the three rivers of the Daliao River watershed. 2,6-Dichloro-4-nitroaniline was generally dominant in the SPM. The levels of nitroaromatic compounds were different among different sites in the Daliao River watershed, mainly caused by the distribution of pollution sources. No obvious correlation was found between the total concentrations of eight nitrobenzenes concentrations and TOC or the slit-clay content of the sediments.

Seasonal Variation of Mercury Associated with Different Phytoplankton Size Fractions in Lahontan Reservoir, Nevada

Sampling is conducted during 2006 in Lahontan Reservoir, Nevada to investigate seasonal variation of total mercury (THg) and methylmercury (MeHg) partitioning in different phytoplankton size fractions as a function of point source (fluvial) mercury (Hg) loads, reservoir residence time, and algal growth. Carson River Hg inputs into the reservoir are extremely dynamic with spring loads two orders of magnitude larger than summer loads. Chlorophyll a measurements show two periods of algal growth. A small amount of algal growth occurs March to May. A second more substantial bloom occurs in the late summer, which is dominated by large, filamentous algae. THg concentrations (Cb) and partitioning coefficients (Kd) in total suspended particulate matter (SPM) are highest when fluvial inputs of Hg-contaminated sediment are large and are not necessarily associated with living biomass. However, MeHg Kd in the small size fraction is indirectly related to fluvial loads and more strongly associated with living biomass in the later portion of the summer when algal growth occurs and reservoir residence times are longer. Data suggest size distinction is important to MeHg partitioning in the reservoir. Lumping all sizes into a single SPM sample will bias the analysis toward low MeHg Cb and low MeHg Kd in late summer when Aphanizomenon flos-aquae dominates the phytoplankton assemblage.

Assessment of fungi and suspended particulate matter in the indoor air of households of Jammu city (J&K)

The present study was conducted to assess status of suspended particulate matter (SPM) and fungi in the indoor air of households located at different sites in Jammu city. The study area was divided into seven sites. At each site, two households were selected randomly and in each household sampling of SPM (µg/m3) and Fungi (CFU/m3) were done twice at three sub sites i.e. bedroom, kitchen and drawing room. Alternaria alternata, Mucor sp., Alternaria sp., Aspergilus niger, A. fumigatus, A. clavatus, A. versicolor, A. glaucus, Fusarium oxysporum, Geotrichum sp. were observed to be the most common fungi in the study area. SPM was found to be maximum (1006µg/m3) in households near water body and minimum (659µg/m3) in the households near hospital. The minimum value of fungal count (20076 CFU/m3) was exhibited by households near National Highway I-A whereas maximum value of fungal count (27226 CFU/m3) was exhibited by the Households located in commercial area. A significant positive correlation (r) was also found between SPM and fungi (+0.06 to +0.62) as well as fungi and relative humidity (+0.10 to +0.60) in the study area.

Mid-chain methoxylated fatty acids within the chemocline of the Cariaco Basin: A chemoautotrophic source?

A series of C 15 –C 20 mid-chain methoxylated fatty acids (FAs) has been tentatively identified in suspended particulate matter samples from within the chemocline of the Cariaco Basin. The concentrations appeared to be highest (50 ng/l) within the core of the chemocline (245–256 m), where they constituted 25% of the total FAs, 9-methoxy-C 16:0 and 10-methoxy-C 16:0 being 73% of the total methoxy acids. Mid-chain methoxy acids in the chemocline had δ 13 C values of ca. −34‰. In stable isotope probing experiments using 13 C labeled bicarbonate and various sulfur species ( S 2 O 3 2 - , SO 3 2 - and particulate S 0 ), up to 80% of 9-/10-methoxy-C 16:0 were 13 C labeled when thiosulfate was provided. Therefore, we propose that mid-chain methoxy FAs are key membrane lipids in sulfur-metabolizing chemoautotrophs within the core of the chemocline. Sulfur-oxidizing bacteria belong to both the ε- and β-proteobacteria; half of the bacteria within the chemocline are either ε-proteobacteria (∼40%) or β-proteobacteria (∼11%), providing a possible clue to the phylogeny of chemoautotrophs and a link to the production of chemoautotrophic biomarkers. We thus demonstrate an association between the presence and activity of sulfur-utilizing chemoautotrophs and occurrence of mid-chain methoxylated FAs within the chemocline of the Cariaco Basin.

Urban and suburban aerosol in Yokohama, Japan: a comprehensive chemical characterization

This article analyses elemental composition of suspended particulate matter (SPM) samples collected monthly from 1999 to 2005 at two locations in Yokohama, Japan. Microwave digestion and inductively coupled plasma mass spectroscopy was employed to measure Mg, Al, Ca, V, Cr, Mn, Ni, Cu, Zn, Ga, As, Se, Rb, Sr, Ag, Cd, Cs, Ba, Pb, and Bi. Water-soluble ions (Na(+), NH(4+), K(+), Ca(2+), Cl(-), NO(3-), and SO(4)2-) and carbonaceous mass (elemental and organic carbon) were detected using ion chromatograph and CHN analyzer, respectively. The results indicate that the composition of SPM on one of the sites is determined by automobile emissions and on the other by industrial combustions. The impact of the emission regulations for automobiles in large Japanese cities, which were enacted during 2002 and 2003, on the SPM composition of the samples is also studied.

Fecal steroids in riverine runoff of the Pearl River Delta, South China: Levels, potential sources and inputs to the coastal ocean

Domestic sewage is a potential source of contamination deteriorating water quality in rivers and coastal environments. The present study determined the concentrations of eight steroids in both filtrate and suspended particulate matter (SPM) samples collected monthly at the eight major riverine runoff outlets of the Pearl River Delta (PRD), South China, from March 2005 to February 2006. The concentration of the eight steroids (sum of which is defined as Sigma(8)steroid) in the filtrate and SPM samples ranged 16.7-1340 ng L(-1) and 0.44-240 microg g(-1), respectively. The filtrate samples contained the highest levels of cholesterol (CHOE) and stigmasterol (STIG) on average, whereas the SPM samples had the largest relative abundances of CHOE and coprostanol (COP). In general, larger proportions of the steroids were associated with SPM than with the filtrate phase. The combined (filtrate plus SPM) concentrations of COP in riverine runoff of the PRD were at the midpoint of the global range in surface water. The concentrations of Sigma(8)steroid and COP in SPM were not significantly correlated with particulate organic carbon (POC), riverine runoff, or SPM concentrations, which indicates the dominance of nonpoint input sources for the occurrence of steroids in the PRD. The annual riverine inputs of Sigma(8)steroid and COP were estimated at 360 and 31.6 tons yr(-1), respectively, and the monthly inputs of both Sigma(8)steroid and COP were positively correlated with monthly runoff discharge. Furthermore, the concentrations of Sigma(8)steroid, COP, and CHOE showed significant temporal and spatial variability. These results can be explained by a combination of climatic characteristics, socioeconomic conditions, and steroid sources. Analyses of the diagnostic indices of COP and background information suggested that riverine runoff from the PRD may have been affected by domestic wastewater, which appeared to be a major COP source to the Pearl River Estuary and South China Sea.

The effects of seston lipids on zooplankton fatty acid composition in Lake Washington, Washington, USA

We collected suspended particulate matter (seston) and zooplankton samples from Lake Washington in Seattle, Washington, U.S.A., over a 10-month period to investigate the effects of food availability on zooplankton fatty acid (FA) composition. The percentage of nutritionally critical omega3 polyunsaturated fatty acids (PUFA) in the seston varied from 8% of the FA pool in midsummer to 30% during the spring diatom bloom. Zooplankton accumulated much higher percentages omega3 PUFA than was available in the seston. In particular, cladocerans preferentially accumulated eicosapentaenoic acid (EPA, 20:5omega3), copepods accumulated docosahexaenoic acid (DHA, 22:6omega3), and both copepods and cladocerans accumulated 18 carbon chain omega3 PUFAs (C18 omega3). By comparison, the FA of zooplanktivorous juvenile sockeye salmon (Oncorhynchus nerka) were strongly dominated by EPA (12.5% +/- 2.1%) and DHA (28.2% +/- 8.7%). The saturated fatty acid and the arachidonic acid (ARA, 20:4omega6) composition of Diaptomus ashlandi was strongly (r2 = 0.76) and moderately (r2 = 0.54) correlated with the prevalence of these FAs in the seston. Furthermore, the DHA content of Diaptomus was moderately correlated with the seston's DHA content (r2 = 0.45) and very strongly correlated with seston EPA (r2 = 0.89). Since EPA was the most prevalent PUFA in the seston and DHA was the most prevalent PUFA in Diaptomus, these results suggest that Diaptomus may synthesize DHA from the EPA in their food. In general, zooplankton species in Lake Washington were strongly enriched with those FA molecules that are most physiologically important for fish nutrition (i.e., ARA, EPA, and DHA), indicating a clear mechanism by which changes in seston composition influence fisheries ecology.

The hydrological regime and particulate size control phosphorus form in the suspended solid fraction in the dammed Huanghe (Yellow River)

The Huanghe River (Yellow River) had been the second largest river in the world in terms of sediment load to the sea; however, the river water discharge and sediment flux to the sea and their seasonal variability have been significantly altered by the dam activities and recent water–sediment regulation. These changes are believed to have important impacts on the flux of phosphorus that is generally transported in particulate form. In this article, the samples of suspended particulate matter (SPM) were collected at the Lijin Station during two high-discharge events in 2005 and were separated by particle size. Sequential extractions were applied to determine the forms of P in different particle size fractions and to assess the potential bio-availability of particulate phosphorus (PP). Based on the in-laboratory measurement, the impacts of different hydrological regimes on the source of PP and its bio-availability were also analyzed. The results indicate that exchangeable, organic, authigenic, and refractory P were preferentially associated with clay, very fine, and fine silt fractions. Detrital P was mainly associated with the medium and coarse silt fractions. Detrital P and authigenic P (two forms of calcium bound phosphorus) were the dominant fractions in all samples. Thus, the potential bio-available PP (exchangeable P and organic P) was mainly associated with the finer particles, such as clay. Higher content of exchangeable, organic, authigenic, and residual P and lower content of detrital P were found during the period of rainstorm compared to that of WSR. P forms and partitioning of P forms among different particle size fractions were assumed to depend on the sources of SPM. It is likely that the pathways and fates of PP forms were controlled by damming and by the related changes of hydrological regime. Therefore, anthropogenic changes of hydrological regime and particle size dominanted the amount and distribution pattern of bio-available P transportation to the estuary and the adjacent sea, which will have profound impacts on the marine ecosystems at the Huanghe River Estuary and even the Bohai Sea.

Polycyclic aromatic hydrocarbons (PAHs) in the water column and sediment core of Deep Bay, South China

The levels of 15 polycyclic aromatic hydrocarbons (PAHs) were determined in seawater, suspended particulate matter (SPM), surface sediment and core sediment samples of Deep Bay, South China. The average concentrations Σ 15PAHs were 69.4 ± 24.7 ng l −1 in seawater, 429.1 ± 231.8 ng g −1 in SPM, and 353.8 ± 128.1 ng g −1 dry weight in surface sediment, respectively. Higher PAH concentrations were observed in SPM than in surface sediment. Temporal trend of PAH concentrations in core sediment generally increased from 1948 to 2004, with higher concentrations in top than in sub-surface, implying a stronger recent input of PAHs owing to the rapid economic development in Shenzhen. Compared with historical data, the PAH levels in surface sediment has increased, and this was further confirmed by the increasing trend of PAHs in the core sediment. Phenanthrene, fluoranthene and pyrene dominated in the PAH composition pattern profiles in the Bay. Compositional pattern analysis suggested that PAHs in the Deep Bay were derived from both pyrogenic and petrogenic sources, and diesel oil leakage, river runoff and air deposition may serve as important pathways for PAHs input to the Bay. Significant positive correlations between partition coefficient in surface sediment to that in water ( K OC) of PAH and their octanol/water partition coefficients ( K OW) were observed, suggesting that K OC of PAHs in sediment/water of Deep Bay may be predicted by the corresponding K OW.

Seasonal and spatial distribution of particulate organic matter in the Bay of Bengal

In this paper, we have assessed the temporal, spatial and depth related variation of suspended particulate organic matter (POM) in the Bay of Bengal. For this purpose, suspended particulate matter (SPM) samples were collected from eight depths (2 to 1000 m) at 9 locations in the Bay of Bengal during July/August 2001 (Southwest monsoon, SWM), September/October 2002 (Fall Inter-monsoon, FIM), and March/April 2003 (Spring Inter-monsoon, SPIM). The SPM samples were analyzed for chlorophyll a (Chl a), particulate organic carbon (POC) and total particulate nitrogen (TPN). The surface concentrations of POC varied from 4.3 to 11.1 µM C, 3.1 to 10.9 µM C, and 4.3 to 9.0 µM C during SWM, FIM, and SPIM, respectively. The levels of SPM, and the concentrations of Chl a, and POC were relatively higher in the offshore compared to the near shore stations, especially during SWM. The POC concentration and its contribution to the SPM were higher in the surface waters, and both decreased with increasing water column depth at most of the stations. The observed decrease with depth of POC indicates heterotrophic uptake and/or dilution by inorganic material, poor in POC. This was also reflected in the C/N ratio which generally increased with water column depth. The relatively low C/N and POC/Chl a ratios, and high Chl a and % POC during the SWM and FIM indicate the presence of relatively fresh POM in the Bay during these two seasons. The observed seasonal differences in the quality of POM appears to be governed by river run-off and the physical forces such as eddies which pump nutrients into the surface waters thereby enhancing biological production.