Petrogenic Inputs Research Articles

Unraveling Environmental Forces Shaping Surface Sediment Geochemical “Isodrapes” in the East Asian Marginal Seas

AbstractAs major sites of carbon burial and remineralization, continental margins are key components of the global carbon cycle. However, heterogeneous sources of organic matter (OM) and depositional environments lead to complex spatial patterns in sedimentary organic carbon (OC) content and composition. To better constrain the processes that control OM cycling, we focus on the East Asian marginal seas as a model system, where we compiled extensive data on the OC content, bulk isotopic composition (δ13C and Δ14C), total nitrogen, and mineral surface area of surficial sediments from previous studies and new measurements. We developed a spatial machine learning modeling framework to predict the spatial distribution of these parameters and identify regions where sediments with similar geochemical signatures drape the seafloor (i.e., “isodrapes”). We demonstrate that both provenance (44%–77%) and hydrodynamic processes (22%–53%) govern the fate of OM in this margin. Hydrodynamic processes can either promote the degradation of OM in mobile mud‐belts or preserve it in stable mud‐deposits. The distinct isotopic composition of OC sources from marine productivity and individual rivers regulates the age and reactivity of OM deposited on the sea‐floor. The East Asian marginal seas can be separated into three main isodrapes: hydrodynamically energetic shelves with coarser‐grained sediment depleted in OC, OM‐enriched mud deposits, and a deep basin with fine‐grained sediments and aged OC affected by long oxygen exposure times and petrogenic input from rivers. This study confirms that both hydrodynamic processes and provenance should be accounted for to understand the fate of OC in continental margins.

Insights about levels and source appointment of petroleum hydrocarbons in Brazilian semi-arid coastal: baseline status assessment for ocean decade targets

The Ocean decade (2021-2030) for sustainable development proclaimed in 2017 by the UN, seeks to promote and conserve the sustainable use of oceans, seas, and marine resources. For this, the distribution of n-alkanes, polycyclic aromatic hydrocarbons (PAHs), and biomarkers, in sediments from the Fortaleza coastal zone (Mucuripe harbor (MH) and Inner Continental shelf (ICS)) were used to assess the impacts of anthropogenic activities in the area. The concentrations of total n-alkanes (Σ16 n-alkanes) in MH and ICS sediments varied from 35.9 to 94.9 and 17.9 to 197.3μgg-1, respectively, while the isoprenoids phytane and pristane in MH and ICS sediments ranged from 0.1 to 1.69 ug g-1 and from 0.14 and 1.20μgg-1, respectively. Most of the sediment samples presented carbon preference index (CPI) values close to unity, indicating that the area is submitted to petroleum-related sources. The concentrations of Σ16 PAHs in MH and ICS sediments varied from 87.0 to 562.0 and 98 to 288.0ngg-1. This work presents the first investigation of the petroleum biomarkers hopanes and steranes in the Fortaleza coastal zone, in which ΣBiomarkers varied from 0.10 to 1.79 and 0.02 to 0.24 ug g-1 in MH and ICS sediments, respectively. The presence at stations of biomarkers also indicates petrogenic input. The diagnosis of the distribution of pollutants in the investigated zones of the Fortaleza coast suggests contamination from urban areas and oil spills and vessel traffic.

Aquatic biomass is a major source to particulate organic matter export in large Arctic rivers

Arctic rivers provide an integrated signature of the changing landscape and transmit signals of change to the ocean. Here, we use a decade of particulate organic matter (POM) compositional data to deconvolute multiple allochthonous and autochthonous pan-Arctic and watershed-specific sources. Constraints from carbon-to-nitrogen ratios (C:N), δ13C, and Δ14C signatures reveal a large, hitherto overlooked contribution from aquatic biomass. Separation in Δ14C age is enhanced by splitting soil sources into shallow and deep pools (mean ± SD: -228 ± 211 vs. -492 ± 173‰) rather than traditional active layer and permafrost pools (-300 ± 236 vs. -441 ± 215‰) that do not represent permafrost-free Arctic regions. We estimate that 39 to 60% (5 to 95% credible interval) of the annual pan-Arctic POM flux (averaging 4,391 Gg/y particulate organic carbon from 2012 to 2019) comes from aquatic biomass. The remainder is sourced from yedoma, deep soils, shallow soils, petrogenic inputs, and fresh terrestrial production. Climate change-induced warming and increasing CO2 concentrations may enhance both soil destabilization and Arctic river aquatic biomass production, increasing fluxes of POM to the ocean. Younger, autochthonous, and older soil-derived POM likely have different destinies (preferential microbial uptake and processing vs. significant sediment burial, respectively). A small (~7%) increase in aquatic biomass POM flux with warming would be equivalent to a ~30% increase in deep soil POM flux. There is a clear need to better quantify how the balance of endmember fluxes may shift with different ramifications for different endmembers and how this will impact the Arctic system.

Combining theoretical concepts and Geographic Information System (GIS) to highlight source, risk, and hotspots of sedimentary PAHs: A case study of Chabahar Bay

Sedimentary PAHs are regionalized variables and their levels, source, and ecological hazards must be discussed in relation to their spatial locations. Our research targeted GIS and Chabahar Bay-Iran to trace spatial variability of PAHs, improve the diagnostic ratios and receptor models in source identification, and determine hotspot of PAH-originated hazards. The entropy Voronoi map distinguished an “entropy strip” in which ∑22PAHs levels increased sharply. Different molecular signatures were individually interpolated and the indicative ratios of distinctive sources were extracted and summed by GIS. The resulting code map reduced potential disagreement among molecular signatures and highlighted the areas where petroleum inputs are prevalent. PCA-MLR analysis extracted three potential sources including fossil fuel combustion (54.36%), petrogenic inputs (29.03%), and vehicle exhaust emissions (16.61%). Interpolated risk layers were re-arranged and overlaid via Fuzzy Membership Functions. The obtained ''Fuzzy AND" map showed the hotspot of the study area in the vicinity of a seasonal estuary.

Petrogenic and Biogenic Inputs of n-alkanes along Shoreline of the Caspian Sea in the Mazandaran Province, North of Iran

The Caspian Sea is the largest lake in the world and is facing an increasing risk of contamination. Sea-based and land-based hydrocarbons inputs are the most critical pollutants of the Caspian Sea. In the present study, n-alkanes and related diagnostic ratios were used to identify the sources of hydrocarbon contaminants in surface sediments along the southern coastal area of the Caspian Sea in Mazandaran province. 27 surface sediment samples were collected from a depth of 5 meters under sea level. Contaminant’s compositions were extracted by Soxhlet apparatus and analyzed by Gas Chromatography-Mass Spectrometry. According to the results, the total concentration of n- alkanes (ΣHC) ranged from 5.2 µg g-1 to 690.7 µg g-1. The S20 (selected station in Noshahr port) had the highest concentration, and most of the stations have levels in a moderate range. Five diagnostic ratios are used to distinguish petrogenic and biogenic contaminants in shorelines of the Mazandaran province. In all stations, Carbon Preference Index (CPI), LMW/HMW, Pr/n-C17, Phy/n-C18, Pr/Phy, and U/R values indicated the petrogenic inputs. However, in some stations biogenic inputs were additionally detected. The petrogenic pollutants were almost from sea-based inputs such as oil spills from Turkmenistan and Azerbaijan. On the other hand, biogenic contaminants were almost from rivers and Hyrcania forests.

Occurrence, characterization, source, and risk assessment of petroleum-related hydrocarbons in sediments along St. Clair River, Ontario, Canada

Total petroleum hydrocarbons (TPH), n-alkanes, petroleum biomarkers, and polycyclic aromatic hydrocarbons (PAHs) were analyzed in the sediments collected from the shorelines and bottom of St. Clair River, Ontario, Canada. Most of the sampling sites had low TPH (< 20 μg/g). River bottom sediment usually had higher level of TPHs, total alkanes, total biomarkers, and total PAHs than most of the shoreline ones. Mixed biogenic and petrogenic n-alkanes were present in all the sites. Most sites had trace amounts of petroleum biomarkers. Mixed pyrogenic and petrogenic inputs with the predominant petroleum, have contributed to the detected PAHs at all sampling sites. PAHs detected would not show potential toxicity to benthic organisms in all shoreline sampling sites; however, some light molecular weight PAHs (e.g., phenanthrene, 2-methyl naphthalene, and acenaphthylene) are anticipated to have possible adverse impacts to sediment-dwelling organisms in part of the river bottom sediment.

Environmental occurrence, spatial distribution, and source identification of PAHs in surface and groundwater samples of Abou Ali River-North Lebanon

This paper assesses the concentrations, spatial distribution, compositional patterns, and sources of polycyclic aromatic hydrocarbons (PAHs) in the dissolved aqueous phase along the Abou Ali River course. The 16 priority PAHs, listed by the USEPA, were investigated in surface- and groundwater samples for 2years starting August 2015 and ending in March 2017. Statistical analysis was done by using the ANOVA test at p < 0.05. The spatial distribution analysis and illustration were done using the ARC GIS software. The total PAHs concentration in surface and groundwater samples varied between not detected to 15.162ngmL-1 and not detected to 0.635ngmL-1, respectively. The highest concentration of PAHs in surface water was observed at site S16, downstream of the river. However, the absence of PAHs was noticed at sites S1 and S2 of the upstream. The contamination levels of PAHs were found to be high in surface water samples, and low in groundwater samples. The 5- and 6-ring PAHs were the most abundant species among others in surface water samples, whereas the 3-ring PAHs were the most abundant in groundwater. Pyrogenic inputs deriving from fuel combustion, incineration, and miscellaneous burning were found to be the main PAH sources in surface and groundwater without ignoring the contribution of petrogenic inputs in some areas.

Spatial and temporal distributions of polycyclic aromatic hydrocarbons in sediments from the Canadian Arctic Archipelago

The concentrations of 23 polycyclic aromatic hydrocarbons (PAHs; 16 parent and 7 alkylated PAHs) were determined in 113 surface marine sediment samples, 13 on-land sediment samples and 8 subsampled push cores retrieved from the Canadian Arctic Archipelago (CAA). PAHs were extracted via accelerated solvent extraction and quantified via gas chromatography–mass spectrometry. The sums of the concentrations of 16 priority PAHs in the surface sediments ranged from 7.8 to 247.7 ng g-1 (dry weight basis, dw). The PAH inputs to the sediments have remained constant during the last century. Source-diagnostic ratios and statistical analysis suggest that the PAHs in the CAA mainly originate from natural petrogenic sources, with some pyrogenic sources. Temporal trends did not indicate major source shifts and largely indicated petrogenic inputs. Overall, the sediments retrieved from the CAA have low PAH concentrations, which indicates a low ecological risk for benthic or other organisms living near the water-sediment interface.

Occurrence, characterization, and ecological assessment of petroleum-related hydrocarbons on the shoreline of Fraser River Delta, British Columbia, Canada

The Fraser River Delta is a unique and dynamic region supporting the diverse ecosystems and habitats in the Canadian West Coast. Total petroleum hydrocarbons (TPH), n-alkanes, petroleum biomarkers, and polycyclic aromatic hydrocarbons (PAHs) were analyzed for the intertidal sediments taken from the shorelines of the Delta area, British Columbia, Canada, to establish the baseline background data. Most of the sampling sites had low TPH (< 40 μg/g); only two samples had TPH from 100 to 150 μg/g. Mainly biogenic n-alkanes were present in all sites. Non-detectable to trace amounts of petroleum biomarkers were found at most sites. Mixed pyrogenic and petrogenic inputs contributed to the presence of PAHs at most sites. PAHs are not present in amounts anticipated negative effects to benthic organisms in all sampling sites, except that benzo (a) pyrene (BaP) from the upper intertidal zone (UIZ) of Burnaby Fraser Foreshore Park may have possible adverse biological effects.

EVOS and the Prince William Sound Long Term Environmental Monitoring Program

ABSTRACT Following the 1989 Exxon Valdez oil spill (EVOS), the Prince William Sound Regional Citizens' Advisory Council began the Long-Term Environmental Monitoring Program (LTEMP) in 1993 to track oil hydrocarbon chemistry of recovering sediments and mussel tissues along the path of the spill in Prince William Sound (PWS) and across the Northern Gulf of Alaska (NGOA) region. The program also samples sites near the Alyeska Marine Terminal (AMT) within Port Valdez, primarily to monitor tanker operations and the resulting treatment and discharge of oil-contaminated tanker ballast water. Over the last 28 years, the program has documented EVOS oil's disappearance at the spill-impacted sites (albeit buried oil still exists at a few unique sheltered locations in PWS). Within the Port, a few tanker- and diesel-spill incidents have been documented over the years, but all were minor and with recovery times of &amp;lt; 1 yr. Of highest concern has been the permitted chronic release of weathered oil from tankers' ballast-water that is treated and discharged at the Alyeska Marine Terminal (AMT). In earlier years (1980s–90s), with discharge volumes reaching 17–18 MGD, up to a barrel of finely dispersed weathered oil would be released into the fjord daily. Over the last two decades, total petrogenic inputs (TPAH43) into the Port have declined as measured in the monitored mussels and sediments. This trend reflects a combination of decreased Alaska North Slope (ANS) oil production and thus, less tanker traffic, plus less ballast from the transition to double-hulled tankers with segregated ballast tanks, and improved treatment-facility efficiency in removing PAH. From the 2018 collections, mussel-tissue hydrocarbon concentrations from all eleven LTEMP stations (within Port Valdez as well as PWS and NGOA regions) were below method detection limits and similar to laboratory blanks (TPAH43 &amp;lt; 44 ng/g dry wt.). At these low background levels, elevated TPAH values from a minor 2020 spill incident at the Terminal were easily detected at all three Port Valdez stations.

Minor changes in biomarker assemblages in the aftermath of the Cretaceous-Paleogene mass extinction event at the Agost distal section (Spain)

The Cretaceous/Palaeogene Boundary (KPgB) represents one of the five major mass extinctions in Earth's history, and determining the nature of associated environmental change and biotic recovery is critical for understanding the history of life on our planet. To explore that, we examined the distributions of selected biomarkers (n-alkanes, acyclic isoprenoids, steranes and hopanes), organic and carbonate δ13C values, total organic carbon contents and major and trace elements in a distal section spanning the KPgB (Agost, SE Spain). The studied Agost section is an ~32 cm-thick bathyal sequence of marlstones, clays and marly limestones, and high sedimentation rates allow high (cm) resolution analysis. These analyses exhibit sample-to-sample variability, but there are few significant differences between pre- and post-KPgB biomarker assemblages, suggesting a rapid recovery of the non-fossilizing phytoplankton community after the KPgB. Despite the persistence of life, the organic matter assemblage is rather variable through the first 10 kyr after the impact event. This interval is associated with changing terrigenous and petrogenic inputs as well as varying redox conditions as reflected by the enrichment factor of uranium (UEF) vs that of molybdenum (MoEF) as well as biomarker indices (gammacerane and homohopane indices). Moreover, sterane distributions do differ between pre- and post-KPgB sediments. Thus, the KPgB impact did affect environmental conditions and non-fossilizing algal and bacterial communities even in distal sites, but these organisms appear to have rapidly recovered, within 10 kyr after the KPgB.

Characterization of polycyclic aromatic hydrocarbons in the surface sediments around the sunken Sanchi oil tanker

The Sanchi oil tanker collision has attracted worldwide attention for its uniqueness in history. This study investigates the contamination level, spatial distribution, sources, and ecological risk level of polycyclic aromatic hydrocarbons (PAHs) present in the surface sediments collected from around the sunken tanker. The results indicated that the total PAH contents in the study area were in the range of 26.42–226.94 ngˑg−1, with an average of 106.86 ngˑg−1. The highest PAH concentration was observed at the station closest to the Sanchi wreckage, indicating potential PAH contamination due to the accident. The PAH ratios and statistical analysis revealed that the PAHs were mainly generated by coal and fuel oil combustion, with certain petrogenic inputs. The ecological risk assessment results suggested that adverse ecological effects to the benthic ecosystem due to PAH contamination was rare. However, long-term monitoring of the local sedimentary environment is highly recommended because of the prominent presence of high molecular weight PAHs.

Seasonal dynamics of polycyclic aromatic hydrocarbons between water and sediment in a tide-dominated estuary and ecological risks for estuary management

Understanding the transportation of polycyclic aromatic hydrocarbons (PAHs) across the water-sediment interface can help researchers to partition their sources while being particularly important for managing PAH input. This study fully explored the PAH dynamics between water and sediment in a tide-dominated estuary. The monthly concentration of ΣPAHs in sediments ranged from 325.47 to 1098.49 ng/g (dry weight), while that in water varied from 154.00 to 725.80 ng/L. The PAH levels found in the present study were relatively high in comparison with other estuarine systems worldwide. The high-molecular-weight PAHs were more readily redissolved from sediment to water, while the low-molecular-weight PAHs were mostly in an unsaturated state with diffusion occurring from water to sediment. The seasonal differences of ΣPAHs were significant and were largely controlled by the changes in sediment properties, marine currents, and water temperature. The diagnostic ratios revealed that predominant sources of PAHs were pyrogenic processes and petrogenic inputs.

Determination of hydrocarbon sources in major rivers and estuaries of peninsular Malaysia using aliphatic hydrocarbons and hopanes as biomarkers

In this study, levels and sources of aliphatic hydrocarbons and hopanes in surface sediments collected from rivers and estuaries of Peninsular Malaysia were assessed. The concentrations of total n-alkanes ranged from 21.19 to 364.54, and the concentrations of hopanes ranged from 0.23 to 2.45 mg kg−1 dry weight. Evaluation of aliphatic diagnostic indices including Carbon Preference Index (CPI), low molecular weight/high molecular weight ratio (LMW/HMW), terrigenous to aquatic ratio (TAR), carbon preference index (CPI), average chain length (ACL) and pristine to phytane indicate mostly petrogenic input especially in estuaries, which is indicative of anthropogenic activities in the study areas. The results also indicate biogenic origin n-alkanes masked by the anthropogenic features in some stations. The hopane ratios indicate hopanes from the Prai and Malacca Rivers were similar to Middle East Crude Oil (MECO), indicating MECO as one of the sources of petroleum hydrocarbons.

Occurrence, characterization, and ecological assessment of petroleum-related hydrocarbons in intertidal marine sediments of Burrard Inlet, Vancouver, British Columbia, Canada

Total petroleum hydrocarbons (TPH), n-alkanes, petroleum biomarkers, and polycyclic aromatic hydrocarbons (PAHs) were analyzed in the intertidal sediments of Burrard Inlet, Vancouver, British Columbia, Canada. Most of the sampling sites had low TPH (<40 μg/g). Only 10% of sampling sites, located nearby a harbour and densely populated areas, had relatively high TPH (<260 μg/g). Main biogenic n-alkanes were present in all the sites, except for the main petrogenic input in the sample from the upper intertidal zone (UIZ) of the Maplewood Mudflats. Most sites had trace amounts of petroleum biomarkers. Mixed pyrogenic and petrogenic inputs contributed to PAHs at most sites. PAHs did not show potential toxicity to benthic organisms at most sites; however, possible negative effects from some of the detected PAHs were found for the samples from the UIZs of the Maplewood Mudflats and Labour View Park, and from the lower intertidal zone (LIZ) of Gates Park.

Occurrence, sources and ecological and human health risks of polycyclic aromatic hydrocarbons in soils from some functional areas of the Nigerian megacity, Lagos.

The study investigated the levels of the USEPA 16 PAHs in soils collected from selected functional areas (cemetery, commercial, industrial and residential areas) of the Nigerian megacity, Lagos. The soil samples were subjected to ultrasonic-assisted extraction in a 1:1 (v/v) mixture of dichloromethane/hexane, and the PAHs in the resulting extracts were determined by gas chromatography-mass spectrometry. The Σ16 PAHs in soils of these functional areas varied between 890-4675, 485-4513, 111-15,577 and 509-2047μgkg-1 for cemetery, industrial, commercial and residential areas, respectively. The benzo(a)pyrene carcinogenic (BaPTEQ) and mutagenic equivalency (BaPMEQ) values of PAHs in these soils spanned from 523 to 1046 and 446 to 1129 µgkg-1, respectively. The hazard index values suggested that there are adverse (non-carcinogenic) health effects for a child's exposure to PAHs in soils of commercial areas. The cancer risk values resulting from an adult's and a child's exposure to PAHs in these urban soils via dermal contact and oral ingestion surpassed the target value of 10-6 which suggested that there is a considerable cancer risk relating to human exposure to PAHs in these urban soils. An ecological risk assessment making use of soil quality guidelines and risk quotients suggested a low ecological risk to organisms in soils of these functional areas except for those from commercial areas. PAH isomeric ratios and principal component analysis indicated that PAHs in these soils arise from petrogenic inputs, such as occasional spills of liquid petroleum fuels and discharges from automobile workshops and generator houses, as well as pyrogenic processes including traffic emissions and combustion of fossil fuels and biomass.

Occurrence and weathering of petroleum hydrocarbons deposited on the shoreline of the North Saskatchewan River from the 2016 Husky oil spill

Following the 16TAN Husky oil spill along the North Saskatchewan River (NSR), the occurrence and natural attenuation of the petroleum hydrocarbons were assessed by analyzing the littoral zone sediments/oil debris collected from July 2016 to October 2017. Husky oil-free, mixed sediment-Husky oil, and Husky oil debris samples were identified for all the collected samples. Shoreline sediments were contaminated by mixed biogenic, pyrogenic and petrogenic inputs prior to the spill. Oil stranded on the shoreline of NSR was moved or buried due to the very dynamic conditions of the shoreline, or cleaned through a series of cleanup activities after the spill. Most normal alkanes were naturally weathered, whereas most of the branched alkanes and all of the saturated petroleum biomarkers remained. Some lighter molecular weight (e.g., 2 to 3-ring) polycyclic aromatic hydrocarbons (PAHs) were lost rapidly after the spill, whereas sulfur containing components, e.g., dibenzothiophenes and benzonaphthothiiophenes, and those having a heavier molecular weight did not change markedly even 15 months post-spill. Similarly, some light hydrocarbons (e.g., <C10) were lost over the first kilometers from the point of entry (POE), while heavier hydrocarbons did not show any major differences away from the POE. Very large inter-site and inter-survey discrepancies were found for samples. Evaporation into the air and dissolution into water, combined with biodegradation, were together or independently the main contributors to the loss of the light molecular hydrocarbons.

First Investigation of Seasonal Concentration Behaviors and Sources Assessment of Aliphatic Hydrocarbon in Waters and Sediments from Wadi El Bey, Tunisia.

The contents, composition profiles, and sources of aliphatic hydrocarbons were examined in surface sediment and water samples collected from Wadi El Bey, in Tunisia, during different year seasons in 14 stations receiving domestic effluent, industrial discharge, and agricultural drainage wastes. The target substances were analyzed by gas chromatography coupled with mass spectrometric detection (GC/MS). Total concentrations of n-alkanes (n-C14-n-C38) ranged from 0.08 ± 0.01 to 18.14 ± 0.1µg/L in waters and 0.22 ± 0.04 to 31.9 ± 24.6µg/g in sediments, while total aliphatic fraction ranged from 0.08 ± 0.01 to 196 ± 140µg/L in waters and 0.22 ± 0.04 to 1977 ± 1219µg/g in sediments, which means that almost all sites were affected by hydrocarbon contents in sediments exceeding the recommended limit (100µg/g). Various diagnostic indices (ADIs) were used to identify the hydrocarbon sources, namely the concentration ratios of individual compounds (n-C17/pristane, n-C18/phytane, pristane/phytane, n-C29/n-C17, n-C31/n-C19) as well as cumulative quantities (Carbon Preference Index, natural n-alkanes ratio, terrigenous/aquatic compounds ratio, unresolved complex mixture percentage, low molecular weight vs. high molecular weight homologues, Alkane Proxy and Terrestrial Marine Discriminants). In general, these indexes indicated that the origin of aliphatic hydrocarbons affecting sediments and waters of Wadi El Bey were linked to both biogenic and petrogenic inputs, attesting the impact of plankton and terrestrial plants and of oil contamination, respectively. The average carbon chain length computation (ACL), used to further index the chemical environment, ranged from 25.5 to 31.1 in sediments and 47.9-116 in waters. This finding could depend on the severe disturbances suffered by the ecosystem as a consequence of heavy anthropogenic inputs. Petroleum contamination associated with high eutrophication rates in Wadi El Bey must be strictly controlled, due to possible harmful effects induced on ecosystem and humans.

Sedimentary record of hydrocarbons and sewage inputs from a highly populated region in South-Eastern Brazil.

The environmental impacts of the urban expansion in Rio de Janeiro was evaluated based on the historical accumulation of black carbon (BC), aliphatic (AHs) and aromatic hydrocarbons (PAHs) and sterols in a sediment core retrieved from Botafogo Cove. BC related to oil combustion sources increased significantly since the 1990s. AHs were associated with petroleum inputs and revealed a high level of contamination. Multivariate statistical methods (a Principal Component Analysis associated with a linear multiple regression - PCA/LMR) applied to PAHs suggests changes in the sources in recent years. This can be ascribed to a reduction in pyrogenic emissions over the last four decades and to an increase in petrogenic inputs since the 1990s. The sterol dinosterol registered the increased eutrophication over the last three decades, but the sewage marker coprostanol was present at relatively low concentrations (0.40 to 1.16 μg g-1) probably caused by enhanced bacterial activity in the sediment.

Spatial distribution and source identification of hydrophobic organic compounds (HOCs) on sedimentary microplastic in Hong Kong

The spatial distribution, composition and source of hydrophobic organic compounds (HOCs) including polyaromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs) and organochlorinated pesticides (OCPs) of the sedimentary microplastics (0.25–5 mm) in Hong Kong were investigated. The concentration of ΣPAHs ranged between 70.8 and 1509 ng g−1 with inter-site differences although the regional difference was insignificant, indicating localised pyrolytic and petrogenic input of PAHs. The concentration of ΣPCBs (13–1083 ng g−1) varied with both study sites and regions with higher concentrations obtained in the western waters, possibly due to the input from Pearl River. Significantly higher concentrations of OCPs on eastern shores highlighted fishing and aquaculture activities in South China Sea a potential major source of OCPs. DDT and its metabolites (DDX, ranged from 1.96 to 626 ng g−1) were the dominant forms of OCPs (45%–80%). Since most of the DDX existed as DDT, this suggested that there was a fresh input of DDT into the microplastics. As microplastics and HOCs cannot be removed effectively from the environment, reduction of potential ecotoxicological risks should rely on minimizing the use of plastics and HOCs.