Coastal Sediment Samples Research Articles

A statistical experiment design approach for optimizing biodegradation of weathered crude oil in coastal sediments

This work studied the bioremediation of weathered crude oil (WCO) in coastal sediment samples using central composite face centered design (CCFD) under response surface methodology (RSM). Initial oil concentration, biomass, nitrogen and phosphorus concentrations were used as independent variables (factors) and oil removal as dependent variable (response) in a 60 days trial. A statistically significant model for WCO removal was obtained. The coefficient of determination ( R 2 = 0.9732) and probability value ( P < 0.0001) demonstrated significance for the regression model. Numerical optimization based on desirability function were carried out for initial oil concentration of 2, 16 and 30 g per kg sediment and 83.13, 78.06 and 69.92 per cent removal were observed respectively, compare to 77.13, 74.17 and 69.87 per cent removal for un-optimized results.

Optically stimulated luminescence dating of young (

The reliability of single-grain optically stimulated luminescence (OSL) dating of young (<500 years old) samples is assessed by examining the results of 166 single-grain OSL analyses of Australian alluvial, lacustrine, estuarine, coastal and marine sediment samples. All samples have been analysed using the modified SAR protocol of Olley et al. [2004b. Optical dating of Holocene sediments from a variety of geomorphic settings using single grains of quartz. Geomorphology 60, 337–358], with burial doses ( D b) calculated by fitting a single Gaussian curve to the peak of a multi-Gaussian summed probability distribution (PDF Gaussian). The near-equivalence of this approach to currently accepted methods of palaeodose estimation – namely the minimum age and central age models of Galbraith et al. [1999. Optical dating of single and multiple grains of quartz from Jinmium rock shelter, northern Australia: part I, experimental design and statistical models. Archaeometry 41, 339–364] – is demonstrated. Considered as a whole, OSL ages calculated using the PDF Gaussian D b determination method are consistent with other chronometric, geomorphological, botanical and historical indicators of depositional age, while four alternative (previously published) methods are generally less reliable when applied to the samples analysed here. The single-grain data from 12 samples of known age (reported by Olley et al. [2004b. Optical dating of Holocene sediments from a variety of geomorphic settings using single grains of quartz. Geomorphology 60, 337–358]) are re-analysed using the PDF Gaussian approach, with all but one yielding a D b consistent with the independently known age. Examples of luminescence data (dose recovery tests, preheat plateaux, continuous-wave and linear-modulated OSL, growth curves, single-grain dose distributions) are provided that together indicate the suitability of Australian quartz for dating young sediments.

Phylogenetic Analysis Indicates Evolutionary Diversity and Environmental Segregation of Marine Podovirus DNA Polymerase Gene Sequences

The distribution of viral genotypes in the ocean and their evolutionary relatedness remain poorly constrained. This paper presents data on the genetic diversity and evolutionary relationships of 1.2-kb DNA polymerase (pol) gene fragments from podoviruses. A newly designed set of PCR primers was used to amplify DNA directly from coastal sediment and water samples collected from inlets adjacent to the Strait of Georgia, British Columbia, Canada, and from the northeastern Gulf of Mexico. Restriction fragment length polymorphism analysis of 160 cloned PCR products revealed 29 distinct operational taxonomic units (OTUs), with OTUs within a site typically being more similar than those among sites. Phylogenetic analysis of the DNA pol gene fragments demonstrated high similarity between some environmental sequences and sequences from the marine podoviruses roseophage SIO1 and cyanophage P60, while others were not closely related to sequences from cultured phages. Interrogation of the CAMERA database for sequences from metagenomics data demonstrated that the amplified sequences were representative of the diversity of podovirus pol sequences found in marine samples. Our results indicate high genetic diversity within marine podovirus communities within a small geographic region and demonstrate that the diversity of environmental polymerase gene sequences for podoviruses is far more extensive than previously recognized.

Effect of solid to solution ratio on biogenic silica determination in coastal sediments

The method of DeMaster (1981) for measuring biogenic silica (BSi) in marine sediments was modified. We found a considerable effect of the solid to solution (S/S) ratio on BSi determination in coastal sediments. The BSi contents determined by DeMaster’s method were overestimated due to the contribution of clay mineral-derived extractable Si at a low S/S ratio ( 2 g l−1). For BSi analysis of coastal sediment samples, the BSi content of representative samples must be measured using various S/S ratios to determine the appropriate S/S ratio in order to minimize the contribution of extractable Si derived from clay minerals and to obtain sufficiently efficient extraction with 1% Na2CO3 before actual sample measurement. One way to determine the appropriate S/S ratio is to use artificial sediment which has a theoretical Si and clay mineral content similar to the sediment sample composition. Using artificial sediment, the S/S ratio of 2 g l−1 seems appropriate for measuring the BSi content of the coastal sediments investigated in this study, because 99.6% recovery can be achieved.

Three-way multivariate analysis of metal fractionation results from sediment samples obtained by different sequential extraction procedures and ICP-OES

Three typical schemes for metal fractionation were applied to analyse coastal surface sediment samples from Bahía Blanca estuary, where an important industrial emplacement is located. Also, three certified reference materials for total metal concentrations were analysed. The studied metals were cadmium, chromium, copper, lead and zinc because of their hazardous potential and related abundance in the estuary. The concentration of metals was determined by inductively coupled plasma-optical emission spectrometry (ICP-OES). A three-way multivariate analysis was performed in order to obtain a better visualization of the experimental data. The extracted information was used to evaluate the equivalence among the results obtained by the three sequential extraction schemes. The data were analysed by parallel factor analysis (PARAFAC). PARAFAC models with two factors describe appropriately the data sets (explained variance about 54% and core consistency of 100%). The multivariate decomposition showed that the three applied schemes are able to describe equally well the behaviour of the metals in the different sediment fractions.

Determination of Polybrominated Diphenyl Ethers in Coastal and River Sediments by Pressurized Liquid Extraction Coupled with Gas Chromatography‐Mass Spectrometry

AbstractThis study presents a time‐ and solvent‐saving method, pressurized liquid extraction (PLE), to extract polybrominated diphenyl ethers (PBDEs) in sediment samples. The effects of various operating parameters (i.e., extraction solution, temperature, pressure, static/dynamic extraction times) for the quantitative extraction of PBDEs by home‐made PLE were systematically investigated and optimized. The analytes were then identified and quantitated by gas chromatography‐mass spectrometry (GC‐MS) in selected ion monitoring (SIM) mode. The 16 PBDE congeners (from tri‐ to deca‐BDE) can be completely extracted by dichloromethane: n‐hexane (3/2, v/v) at 100 °C and 100 atm combined with 15 min static and then 15 min dynamic extraction steps. Recovery of PBDEs in spiked sediment samples ranged from 52 to 104% with 2‐16% RSD, except for BDE‐206. Limits of quantitation (LOQ) were established between 4 and 400 pg/g (dry weight) in 10 g of sediment sample. The extraction efficiency of the PLE was also compared with the traditional Soxhlet extraction method. The total contents of PBDEs ranged from 8.0 to 37.9 ng/g (dry weight) in various river and coastal sediment samples in Taiwan. Deca‐BDE (BDE‐209) was the major PBDE detected in these sediment samples.

Elemental distribution of coastal sea and stream sediments in the island-arc region of Japan and mass transfer processes from terrestrial to marine environments

Abstract A total of 49 elements have been identified in 338 coastal sea sediment samples collected from an area situated off the Ise-Tokai region of Japan for a nationwide marine geochemical mapping project. The spatial distribution patterns of the elemental concentrations in coastal seas along with the existing geochemical maps in terrestrial areas were used to define the natural geochemical background variation, mass transport, and contamination processes. The elemental concentrations of coastal sea sediments are determined primarily by particle size and regional differences. Most elemental concentrations increase with a decrease in particle size. Some elements such as Ca, Mn, and Yb are found to exist in large quantities in coarse particles containing calcareous shells, Fe–Mn oxides, and felsic volcanic sediments. Regional differences reflect the mass transfer process from terrestrial areas to coastal seas and the influence of the local marine geology. An analysis of variance (ANOVA) reveals that for many elements, the particle size effect is predominant over regional difference. The mean chemical compositions of coastal sea sediments are similar to those of stream sediments in adjacent terrestrial areas and in the upper crust of Japan. This observation supports the fact that coastal sea sediments have certainly originated from terrestrial materials. However, the spatial distributions of elemental concentrations are not always continuous between the land and coastal seas. The scale of mass movement observed in marine geochemical maps occurs at a distance of 20 km from the river mouth. A detailed examination of the spatial distribution patterns of K (K2O) and Cr concentrations suggests that terrestrial materials supplied through rivers are deposited near the shore initially, and then gravity-driven processes shift the sediments deeper into the basin. Contamination with heavy metals such as Zn, Cd and Pb was observed in coastal bays surrounded by urban and industrial areas. It is noteworthy that the areas with the highest concentration of these elements usually do not occur near the shore (not near the contamination source) but at the center of the bay. Unexpected low concentrations of Zn, Cd and Pb near shore may either be due to a decreased anthropogenic load in the most recent sediments or to dilution by unpolluted flood sediments.

Application of pressurized fluid extraction technique in the gas chromatography–mass spectrometry determination of sterols from marine sediment samples

In order to determine steroid compounds in GC/MS an analytical method using pressurized fluid extraction (PFE) was developed. While extracting in-house reference material (coastal sediment) typical recovery in PFE ranged from 80 to 120% (±2.5–14.5) and the average extraction yield in PFE in comparison to conventional soxhlet extraction was 115%. In particular, the PFE showed higher extraction efficiency for C 29 and dien sterols. Optimizing parameters such as temperature and pressure is critical in achieving this efficiency. Sterols in the sediment were derivatized with silyl reagent BSTFA in acetone for the final determination. A short column florisil cleanup offered the best separation of the GC/MS sensitive derivatives from co-contaminants. Thirty-three coastal sediment samples were analyzed using PFE and Soxhlet extraction methods. The results on extraction efficiency, silyl derivatization kinetics and purification efficiency demonstrated that PFE is far superior in extracting sterols from sediment samples. It is simple, fast, efficient and amenable for automation.

The Distribution and Sources of Polycyclic Aromatic Hydrocarbons in Surface Sediments Along the Egyptian Mediterranean Coast

Coastal marine sediment samples were collected from 31 sampling stations along the Egyptian Mediterranean Sea coast. All sediment samples were analyzed to determine aliphatic and polycyclic aromatic hydrocarbons (PAHs) as well as total organic carbon (TOC) contents and grain size analysis. Total concentrations of 16 EPA-PAHs in the sediments were varied from 88 to 6338 ng g(-1) with an average value of 154 ng g(-1) (dry weight). However, the concentrations of total aliphatic were varied from 1.3 to 69.9 ng g(-1) with an average value of 15.6 ng g(-1) (dry weight). The highest contents of PAHs were found in the Eastern harbor (6338 ng g(-1)), Manzala (5206 ng g(-1)) and El-Jamil East (4895 ng g(-1)) locations. Good correlations observed between a certain numbers of PAH concentrations allowed to identify its origin. The average total organic carbon (TOC) percent was varied from 0.91 to 4.54%. Higher concentration of total pyrolytic hydrocarbons ( summation operatorCOMB) than total fossil hydrocarbons ( summation operatorPHE) declared that atmospheric fall-out is the significant source of PAHs to marine sediments of the Egyptian Mediterranean coast. The selected marked compounds, a principal component analysis (PCA) and special PAHs compound ratios (phenanthrene/anthracene vs fluoranthene/pyrene; summation operatorCOMB/ summation operatorEPA-PAHs) suggest the pyrogenic origins, especially traffic exhausts, are the dominant sources of PAHs in most locations. Interferences of rather petrogenic and pyrolytic PAH contaminations were noticed in the harbors due to petroleum products deliveries and fuel combustion emissions from the ships staying alongside the quays.

Microbial status in seawater and coastal sediments during pre‐ and post‐tsunami periods in the Bay of Bengal, India

AbstractTsunami, the natural disaster, which occurred on December 26, 2004 in the Indian Ocean, caused severe damage to mankind in the coastal areas. Total loss of life and economic loss because of this disaster have been estimated by various agencies but its effect on microbial density has not been probed. With our previous results on microbial populations in four locations of the Chennai coast of the Bay of Bengal, India in the pre‐tsunami period, the change in microbial populations was studied after the tsunami at regular intervals in the same locations. Coastal sediment and seawater samples were collected from four different locations after 5–10 h and thereafter at intervals of every 7 days up to 28 days post‐tsunami. Bacteria, fungi and actinomycetes were isolated from the marine samples by serial dilution on respective media. Before the tsunami, the bacterial population was higher in seawater samples than the sediments, whereas fungi and actinomycetes were recorded only in the sediments. The microbial population remarkably increased 5–10 h post‐tsunami in all the marine samples irrespective of the location. However, it slowly declined in the subsequent days and became similar to that of the population recorded before the tsunami. The population of gram‐positive bacteria increased whereas the gram‐negative bacterial population decreased after the tsunami. Further, populations of pathogenic bacteria such as coliform and vibrios did not increase after the tsunami. It has been observed that the increase in populations of bacteria and actinomycetes even after 28 days of tsunami may be due to the introduction of foreign microorganisms that developed the ability to survive in the extreme environment by exhibiting special characteristics such as pigmentation and production of exopolysaccharides.

Determination of gamma-emitting radionuclides in the inter-tidal sediments off Balochistan (Pakistan) Coast, Arabian Sea

Natural radionuclide contents of 226Ra, 228Ra and (40)K were studied for inter-tidal sediments collected from selected locations off the745 km long Balochistan Coast using HPGe detector based gamma-spectrometry system. The sampling zone extends from the beaches of Sonmiani (near Karachi metropolis) through Jiwani (close to the border of Iran). The natural radioactivity levels detected in various sediment samples range from 14.4 +/- 2.5 to 36.6 +/- 3.8 Bq kg(-1) for 226Ra, 9.8 +/- 1.2 to 35.2 +/- 2.0 Bq kg(-1) for (228)Ra and 144.6 +/- 9.4 to 610.5 +/- 23.9 Bq kg(-1) for (40)K. No artificial radionuclide was detected in any of the marine coastal sediment samples. 137Cs, (60)Co, 106Ru and 144Ce contents in sediment samples were below the limit of detection. The measured radioactivity levels are compared with those reported in the literature for coastal sediments in other parts of the world. The information presented in this paper will serve as the first ever local radioactivity database for the Balochistan/Makran Coastal belt of Pakistan. The presented data will also contribute to the IAEA's, Asia-Pacific Marine Radioactivity Database (ASPAMARD) and the Global Marine Radioactivity Database (GLOMARD).

Chemical contamination and sediment toxicity along the coast of Corsica

Trace metals (Cd, Pb, Cu, Cr, Ni, Co, Zn, Hg, As, Mn, Al, Fe, and Li) and organic compounds (PCBs, PAHs, lindanes, and DDT and its degradation products) were measured in coastal sediment samples from 27 sites in lagoons and along coastal areas of Corsica. An oyster embryo bioassay evaluated the toxicity of sediments from sites in three coastal lagoons (Urbino, Diane, and Biguglia) and the west coast of Cape Corsica. Despite contamination levels generally lower than those in other Mediterranean coastal areas, contamination is found in specific sites in Corsica and includes natural arsenic contamination on the east coast, insecticide pollution (persistent lindane and DDT) in many areas, both cadmium and lead contamination around Sagone, general contamination of both main harbours (Bastia and Ajaccio) and their surrounding areas, and asbestos mining residues in western Cape Corsica. Monitoring development of Crassostrea gigas embryos showed toxic effects at sites near a factory on Cape Corsica, with up to 100% mortality of larvae, and lower levels of toxicity at Sagone (44% mortality) and in the three coastal lagoons (up to 28% mortality). Results of this regional study show the need for further monitoring to understand the environmental issues facing the Corsican coast.

Speciation of Organometallic Compounds in Environmetal Samples by Gas Chromatography after Flow Preconcentration on Fullerenes and Nanotubes

The development of a simple speciation method for the determination of lead (trimethyllead(I), dimethyllead(II), triethyllead(I), and diethyllead(II)), mercury (methylmercury(I), ethylmercury(I), mercury(II)), and tin (n-butyltin(III), di-n-butyltin(II), tri-n-butyltin(I), tin(IV)) compounds in environmental samples was described. The potential of C70 fullerenes and multiwalled carbon nanotubes (MWNTs) as sorbents was investigated for the first time; this study revealed that there are no significant differences between them in terms of sensitivity, selectivity, precision, and reusability. Comparative studies showed that MWNTs and C60 and C70 fullerenes were superior to graphitized carbon black and RP-C18 for the extraction of the 11 compounds studied. The accuracy of the MWNT method was evaluated from recovery values with two standard reference coastal sediments, and good concordance in the results were obtained. Detection limits of 0.5-2 pg/mL were obtained when using a sorbent column containing 160 mg of MWNTs (sample breakthrough, 50 mL of water). The method was successfully applied to the determination of lead, mercury, and tin compounds in water and coastal sediment samples with satisfactory results.

Speciation analysis of mercury and tin compounds in water and sediments by gas chromatography–mass spectrometry following preconcentration on C 60 fullerene

A simple method for the determination of mercury and tin compounds in water and sediments by solid-phase extraction–gas chromatography–mass spectrometry is proposed. The analytes are complexed with sodium diethyldithiocarbamate, retained on a C 60 fullerene column and eluted with ethyl acetate containing sodium tetra- n-propylborate as derivatizing reagent. The analytical figures of merit of the proposed method in the selective ion monitoring mode include: limits of detection from 0.8 to 1.5 pg ml −1 (sample volume 50 ml) and precision (as relative standard deviation) from 6.2 to 7.4%. The method is quite selective: the determination of mercury and tin species is subject to no interferences from metal ions such as Zn 2+, Fe 3+, Sb 3+, As 3+, Pb 2+, Ni 2+, Cu 2+, Co 2+, Mn 2+and Cd 2+. The accuracy of the method was evaluated from recovery values and the analysis of two standard reference coastal sediments (CRM 462 and CRM 580). The method was also applied to the determination of mercury and tin compounds in water and coastal sediment samples.

Biogeographic and Quantitative Analyses of Abundant Uncultivated γ-Proteobacterial Clades from Marine Sediment

16S rRNA gene-based molecular analyses revealed the presence of several large and so far uncultivated clades within class gamma-Proteobacteria, designated gamma-proteobacterial marine sediment (GMS) clades 1 to 4, in marine sediment. The GMS clades appear only indigenous to marine sediment and so far have an unknown functionality. SYBR Green-based real-time PCR analyses using GMS clade-specific primers indicated GMS clades were a significant part of the bacterial community (0.3-8.7% of total 16S rRNA genes) in both polar and temperate marine sediment samples. Univariate statistical analyses indicated that GMS clade communities were indistinguishable in two temperate coastal sediment samples even though these possessed very different mean grain sizes, organic contents, and organic loading rates. GMS clade communities were slightly different (p < 0.05) between polar and temperate sites, suggesting that psychrophilic adaptation among GMS clade taxa corresponds only to subtle phylogenetic differences. Similar levels of difference were also observed through a sediment core reflecting that through the sediment core history, which spanned approximately 3000 years, GMS clonal diversity shifted only marginally.

Characterization of depth-related changes and site-specific differences of microbial communities in marine sediments using quinone profiles

Respiratory quinone compositions were analyzed by a high-performance liquid chromatography to characterize the depth-related changes and site-specific differences of microbial communities in marine sediments. Two deep-sea sediment samples and one coastal sediment sample were investigated from three sites on the coast of Japan, Sagami Bay, Suruga Bay and Tokyo Bay. Although depth-related changes in microbial community structures were observed, site-specific differences appeared to have greater influence on overall community structures. A variety of quinone homologs was commonly identified at all sampling sites and depths examined, but a few minor quinone fractions, mainly derived from Actinobacteria, were detected only at specific sampling sites. Methylmenaquinone-7 (MMK-7) was the major component throughout the examined depths in Sagami Bay and Tokyo Bay. Most abundant quinone homologs changed with each depth in Suruga Bay. Menaquinone-6 (MK-6) predominated in the 0 to 2-cm layer (19%). Below 0–2cm, the most abundant homolog in each sampling depth was phylloquinone (K1; 13%, 4–6 cm), MK-8 (19%, 8–10 cm) and MK-7 (13%, 16–18 cm). The microbial respiratory quinone profiling method shown here, successfully demonstrates the usefulness of this approach to characterize microbial communities in marine sediments.

Butyltins in water, biofilm, animals and sediments of the west coast of India

Biofilm, fish, oyster, mussel, clam, surface seawater, suspended particulate matter (SPM), and sediment samples were collected from marine and/or estuarine waters of the west coast of India. These samples were analysed for butyltin derivatives such as dibutyltin (DBT) and tributyltin (TBT). The concentrations DBT plus TBT varied between 2.4 and 8.3, 163 and 363 ng/l, 5 and 2853 ng/g dry wt in the SPM, seawater and sediment samples, respectively, of the Marmugao harbour. The values of DBT plus TBT ranged between 0.60 and 29, 123 and 242 ng/l and 1.4 and 65 ng/g dry wt in SPM, water and sediment samples, respectively, collected from the Mandovi estuary. In the Dona Paula Bay the DBT plus TBT varied from 10 to 89 ng/l in surface seawater, and TBT from 10 to 513 ng/g in biofilm samples. For the coastal sediment samples the concentration of DBT plus TBT ranged between 36 and 133 ng/g dry wt of sediment. For the animal samples the DBT plus TBT ranged between 58 and 825 ng/g dry wt of the tissue. Mussel tissues contained the highest amount of DBT plus TBT (825 ng/g dry wt tissue), whereas highest TBT concentration was recorded in the oyster (732 ng/g dry wt). TBT was generally the most abundant butyltin compound in most of the samples suggesting fresh inputs and/or less degradation of TBT. A wide range of the observed butyltin concentrations suggests the presence of localized areas of contamination. Leaching of tributyltin-containing antifouling paints from the ocean going ships, fishing and recreational boats, barges, and the inputs of TBT from the Goa shipyard and dry dock facility situated in the harbour are the probable sources of the DBT and TBT in the samples of the west coast of India. Higher levels of TBT were observed in biofilm relative to that in the surrounding seawater. When fed on TBT contaminated biofilm of the diatom Navicula subinflata, butyltin concentrations in the clam Paphia malabarica increased over the period of feeding suggesting the importance of biofilm in the transfer of butyltins to higher group of organisms.

Vellaria zucchellii sp. nov. a new monothalamous foraminifer from Terra Nova Bay, Antarctica

Vellaria zucchellii sp. nov. is described from coastal sediment samples from Terra Nova Bay (Ross Sea, Antarctica, 74°40′28.1″S, 164°04′11.6″E, Tethys Bay, 25 m depth). This organic-walled monothalamous (single chambered) foraminifer is characterized by a wide, prominent aperture that facilitates attachment to larger particles (small sand grains or other foraminiferal shells). It shares this feature with the two other known species of Vellaria, both of which were described from an Indian estuary. Phylogenetic analysis of small subunit rRNA gene sequences suggest that V. zucchellii is related to the genus Psammophaga. However, the new species lacks the mineral grain inclusions that are characteristic of Psammophaga. The description of this new organic-walled monothalamous foraminiferal species further documents the high taxonomic diversity of these delicate and abundant protists in the polar benthic communities.

Psychrobacter maritimus sp. nov. and Psychrobacter arenosus sp. nov., isolated from coastal sea ice and sediments of the Sea of Japan.

Four strains of Gram-negative, aerobic, psychrotolerant, non-motile, non-pigmented bacteria were isolated from coastal sea-ice and sediment samples. These strains displayed the general chemotaxonomic and phenotypic features of members of the genus Psychrobacter. 16S rRNA gene sequencing positioned the three isolates KMM 3646T, KMM 3643 and KMM 3645 and isolate KMM 3659T in two distinct lineages within the genus Psychrobacter, displaying less than 98.5 % sequence similarity to the type strains of other Psychrobacter species. Genomic distinctness was supported by phenotypic differences in growth temperatures, salinity range for growth and metabolic properties. Based on a combination of phenotypic and biochemical characteristics and phylogenetic position, it is proposed that the members of these two distinct lineages represent two novel species, for which the names Psychrobacter maritimus sp. nov. (type strain Pi2-20T = KMM 3646T = DSM 15387T) and Psychrobacter arenosus sp. nov. (type strain R7T = KMM 3659T = DSM 15389T) are proposed.

Distribution and sources of polycyclic aromatic hydrocarbon (PAH) in marine environment of China

Polycyclic aromatic hydrocarbons (PAHs) are potentially carcinogenic and mutagenic compounds that have raised considerable environmental concern. The highest concentrations of PAHs in the coastal sediment samples in China was 5.8–11.0μg/g (dry weight) in the core from the Huangpu River, Shanghai. The second highest concentration of PAHs was 4.42μg/g (dry weight) in surface sediment of Victoria Harbour in Hong Kong, and 5.73μg/g (dry weight) in sediment of Jiaozhou Bay, Qingdao City. The low concentrations of PAHs were always in the sediments far away from industrial zones and cities, and ranged from 0.10 to 0.30μg/g (dry weight). Several environmental parameters are considered for the identification of sources of PAHs in marine environment. High proportion of naphthalene, low molecular weight PAHs and alkylated PAHs, plus high ratio of phenanthrene to anthracene (>15) and low ratio of fluoranthene to pyrene (<1) suggested a petrogenic source. According to these parameters, the Changjiang (Yangtze) River estuary of Shanghai, Jiaozhou Bay of Qingdao City, Zhujiang (Pearl) River mouth, Jiulong River mouth and most of Hong Kong coastal waters were heavily contaminated by PAHs from petrogenic sources. However, PAHs in rural coastal areas were dominated by pyrolytic origin PAHs. This review clearly showed that oil pollution and incomplete combustion of oil, coal and biomass are the main reason for PAHs anormalies in the study areas.