Alaa R. Mostafa

Distribution and characteristics of PAHs in sediments from the Mediterranean coastal environment of Egypt

To assess the contamination of polycyclic aromatic hydrocarbons (PAHs) in the Mediterranean coastal environment of Egypt, 26 sediment samples from the coastline, harbours, estuaries and coastal lakes were collected and analyzed. The sediment PAH concentrations of thirty-nine 2-6 ring PAHs ranged from 13.5 to 22,600 ng/g. PAH profiles varied according to the nature of the site and its proximity to sources. Industrialized and urbanized region showed high level of PAHs contamination. In general, the contamination levels of PAHs were similar to those observed in contaminated and slightly contaminated sediments of the Mediterranean Sea. Molecular indices based on ratios of selected PAH concentrations were used to differentiate PAHs from pyrogenic and petrogenic and mixed origins. Good correlations were observed between the petrogenic index, MP/P, A-PAHs/P-PAHs and HMW/LMW. Finally, PAH levels in sediments were compared with Sediments Quality Guidelines (ERM-ERL) for evaluation of probable toxic effects on organism.

Risk assessment of polycyclic aromatic hydrocarbons in a Mediterranean semi-enclosed basin affected by human activities (Abu Qir Bay, Egypt).

The contamination of sediments and mussels sampled from Abu Qir Bay by polycyclic aromatic hydrocarbons (PAHs) was investigated. Concentrations of PAHs recorded in the bay sediments ranged from less than MDL to 2660 microg/kg dw. In general, concentrations of PAHs in mussels were higher than their corresponding sediment concentrations reflecting their great bioavailability (242-3880 microg/kg dw). The highest concentration was observed in the western part of the bay, a location affected by intensive shipping activities. The distribution pattern of PAHs was similar for mussels and sediments, particularly for sediments characterized by high contamination level, and they were dominated by the high molecular weight PAHs (4-6-rings). Applying different PAHs ratios, it was found that PAHs originated predominantly from the pyrogenic source either from the combustion of grass, wood and coal (majority of the samples) or from petroleum combustion (harbour area). The output of a Screening Level Ecological Risk Assessment (SLERA) on the bay sediments revealed that adverse ecological effects to benthic organisms are expected to occur in only one sample, and thus PAHs are not considered as contaminants of concern in Abu Qir Bay. Also adverse health effects are not expected to occur from the consumption of the investigated mussels with respect to PAHs in Abu Qir Bay.

Application of a Multimolecular Marker Approach to Fingerprint Petroleum Pollution in the Marine Environment

In an attempt to investigate the suitability of a multibiological marker approach for defining the origin of petroleum pollution in marine systems, the aliphatic hydrocarbon compositions of tar ball samples collected from the beaches of a small island impacted by heavy tar loads were determined by gas chromatography and gas chromatography/mass spectrometry. The tar ball samples, as collected, were at low stages of biodegradation and had diverse physical appearance. The majority of the samples (as many as 7 of the 10) appeared to be heavy fuel oils—possibly Bunker C. The GC traces for the other three tar balls, however, indicated that they were crude oils probably from tanker ballast washings or other non-point sources like the oil entering from the adjacent North Mediterranean. The biomarkers of the sterane and hopane series in these samples, however, had remained unaffected by weathering, and their distributions revealed significant differences among the samples suggesting multiple sources of the tar balls. The tar ball samples could be genetically subdivided into four groups on the basis of their biomarker fingerprints. A marine carbonate or evaporite, hypersaline, anoxic depositional environment of the petroleum source rock for Type I residues could be inferred from the even-carbon-number predominance of n-alkanes, the high relative abundance of gammacerane and the predominance of C35 relative to C34 17α(H)-homohopanes. Higher plant contribution and a deltaic environment of source rock deposition could be concluded for Type II residues from the high concentrations of oleanane and diasteranes. On the other hand, Type III residues possessed geochemical characteristics consistent with a normal marine carbonate or evaporite source depositional environment under normal saline, reducing conditions. Finally, type IV residues had biomarker signatures intermediate between Types II and III.

Application of Petroleum Hydrocarbon Chemical Fingerprinting in Oil Spill Investigations––Gulf of Suez, Egypt

Abstract In an attempt to examine the suitability of chemical fingerprinting methods in oil spill investigations, multiple parameters sensitive to both sources and degree of weathering were used to characterize spilled oil samples and to distinguish spilled hydrocarbons from sources unrelated to the spill in shoreline of the Gulf of Suez, Egypt. The characterizations of individual aliphatic and aromatic compounds were based on gas chromatography and gas chromatography/mass spectrometry analyses. The distribution of n-alkanes, polynuclear aromatic hydrocarbons (PAHs) and alkyl PAHs in the source oil and an oil slick collected 72 h after the spill were very similar. Major compositional changes observed in a weathered oiled sediment collected nine months after the spill from the shoreline at the spill location were consistent with previous studies. Molecular parameters of hopane and sterane biomarkers were very similar in the source oil, the spilled oil and the highly weathered oiled sediment. The similarity in biomarker compositions provided a strong evidence for a close genetic association of these samples. Ratios of C2-chrysenes/C2-phenanthrenes and C2-chrysenes/C2-dibenzothiophenes, the pregnane index (sum of the concentrations of C21 and C22 steranes over total concentration of steranes×100), and the tricyclic terpane index (sum of the concentrations of C19 and C30 tricyclic terpanes over total concentration of terpanes×100) clearly differentiated the refined oil products from crude oils. The composition of bilge oil indicated enrichment of late eluting steranes and terpanes and showed biomarker distributions similar to natural petroleum. The results further support that sterane and terpane biomarker analyses could differentiate oil samples of different sources even though they were sometimes indistinguishable in PAH and alkane compositions.

Source-dependent biomarker properties of five crude oils from the Gulf of Suez, Egypt

Abstract Five crude oils from some producing wells in the southern part of the Gulf of Suez were characterized using a variety of organic geochemical parameters. The results reveal significant differences within the oils from the Gulf of Suez basin that suggest two oil types and one mixed type. Type 1 oils from Ras Fanar and East-Zeit fields show a high relative abundance of gammacerane indicating a marine saline-source depositional environment. Another related feature of these oils is the predominance of C 35 over C 34 17α( H )-homohopanes. Type 2 oils from Gama and Amal-9 wells show oleanane indices over 20%, indicating that they originated from an angiosperm-rich, Tertiary source rock. Type 3 oil from Amal-10 well has geochemical characteristics intermediate between those of types 1 and 2. This may reflect mixing of oils from the sources of both types 1 and 2. The geochemical characteristics of the oils vary sufficiently to suggest multiple sources. The type 1 oils possess geochemical characteristics consistent with Upper Cretaceous Brown Limestone or Lower Eocene Thebes Formation carbonate source rocks. Type 2 oils are very similar in geochemical character to the Lower Miocene Rudeis Formation source rocks.

Assessment of persistent organochlorine pollutants in sediments from Lake Manzala, Egypt

Organochlorine pesticides (OCPs) and polychlorinated biphenyls (PCBs) were determined in surface and core sediment samples collected from Manzala Lake, the largest of the Egyptian coastal lakes. Total concentrations of OCPs and ∑7 PCBs (ICES) in sediments ranged from 0.63 to 31.31 ng/g and 0.26 to 31.27 ng/g, respectively. Geographical distribution indicates that levels of contaminants were significantly higher in areas which are mainly influenced by municipal discharge, indicating significant sources of these compounds in urbanised areas. The composition of DDT and its metabolites suggest old input of DDT. The levels of contaminants in Manzala Lake were similar or lower than those observed in comparable areas worldwide. The profiles of ∑OCPs and ∑PCBs in a core from a site heavily impacted by sewage discharge have highest concentrations in the surface core section indicating recent inputs. Assessment of ecotoxicological risk indicated that sediments in two sites were likely to pose potential biological adverse impact.

Spatial distribution and temporal trends of persistent organochlorine pollutants in sediments from Lake Maryut, Alexandria, Egypt.

Organochlorine compounds (OCs) in surface and core sediments collected from Lake Maryut, Egypt, were examined to elucidate their distribution, ecological risk and historical trend. To our knowledge, this is the first study on residue levels of OCs in sediments from Lake Maryut. Concentrations of PCBs and DDTs were higher than other OCs, ranging from 3.06 to 388 and from 0.07 to 106 ng/g dry wt., respectively. The highest concentrations of OCs were found at stations near the discharge point of sewage and close to industrial areas. The distribution of DDT and its metabolites suggest no recent inputs into the lake environment. Contamination levels of sedimentary PCBs and DDTs, can be categorized moderate to high compared to other urbanized regions worldwide. Temporal trends in OCs levels were influenced by input pathways at two sites. Evaluation of ecotoxicological risks suggests that adverse biological effects are expected mainly in the main basin area.

Distribution and ecological risk of organochlorine pesticides and polychlorinated biphenyls in sediments from the Mediterranean coastal environment of Egypt

Organochlorine contamination in the Mediterranean coastal environment of Egypt was assessed based on 26 surface sediments samples collected from several locations on the Egyptian coast, including harbors, coastal lakes, bays, and estuaries. The distribution and potential ecological risk of contaminants is described. Organochlorine compounds (OCs) were widely distributed in the coastal environment of Egypt. Concentrations of PCBs, DDTs, and chloropyrifos ranged from 0.29 to 377ngg(-1) dw, 0.07 to 81.5ngg(-1) dw, and below the detection limit (DL) to 288ngg(-1) dw, respectively. Other organochlorinated pesticides (OCP) studied were 1-2 orders of magnitude lower. OCP and PCBs had higher concentrations at Burullus Lake, Abu Qir Bay, Alexandria Eastern Harbor, and El Max Bay compared to other sites. OCP and PCB contamination is higher in the vicinity of possible input sources such as shipping, industrial activities and urban areas. PCB congener profiles indicated they were derived from more than one commercially available mixture. The ratios of commercial chlordane and heptachlor metabolites indicate historical usage; however, DDT and HCHs inputs at several locations appear to be from recent usage. The concentrations of PCBs and DDTs are similar to those observed in sediments from coastal areas of the Mediterranean Sea. Ecotoxicological risk from DDTs and PCBs is greatest in Abu Qir Bay, Alexandria Harbor, and El-Max Bay.

An Overview of Metal Pollution in the Western Harbour of Alexandria, Egypt

Limited data are available on the concentration of metals in sediments in the Western Harbour of Alexandria. The most comprehensive record is from a survey conducted more than a decade ago. Industrial and human activities in and around this area have increased dramatically in the last 20 years. The purpose of this study was to determine the concentrations of heavy metals in surfacial bottom sediments of the harbor, to assess their potential biological effects and to identify their possible sources. Sediment samples from 21 stations throughout the harbor were analyzed for grain size, total organic carbon content (TOC), and metals (Al, As, Ba, Be, Cd, Cr, Cu, Fe, Mg, Mn, Ni, Pb, Se, Sn, V, and Zn) to assess the extent of contamination in the area. The results indicated that concentrations of metals in the sediments varied widely depending on the location. High levels of metals were observed in the Arsenal Basin and the outfall area of El Mahmoudiya Canal in the inner harbor. The concentrations of metals were found to be higher than those recorded in the previous study. However, with some exceptions, most of the changes in the metal concentrations could be accounted for by the variations in aluminum, which represents the variations in mineralogy and grain size, indicating that the majority of the metals were of “natural” origin. The present data were also compared with results from other areas.

Risk posed by chlorinated organic compounds in Abu Qir Bay, East Alexandria, Egypt

IntroductionIn Egypt, the picture of threats to humans and the environment from the exposure to organic pollutants is still incomplete. Thus the objectives of this study were to assess the occurrence and distribution of polychlorinated biphenyls (PCBs), organochlorine pesticides, and chlorpyrifos in sediments and mussels of Abu Qir Bay and their risks for environment and human health.Materials and methodsTwenty-three different compounds organochlorines were determined in 20 surfacial sediment and 10 mussel samples by gas chromatography-electron capture detector. A Screening Level Ecological Risk Assessment (SLERA) and a Human Health Risk Assessment (HHRA) were performed with the data.Results and discussionΣDDT (DDT, DDE, DDD) (average concentration 27 µg/kg dw) dominated the detected organic pollutants in the sediments, followed by CHLs (chlordane, heptachlor, heptachloro epoxide), hexachlorocyclohexane, chlorpyrifos, endosulfane, dieldrine, Σ6 PCBs, aldrine, hexachlorobenzene, pentachlorobenzene, methoxychlor, and mirex. In general, concentrations of Σ6 PCBs in mussels were higher than their corresponding sediment concentrations reflecting their relatively high bioavailability and bioaccumulative potential. However, concentrations of the organochlorine pesticides in mussels were lower than their corresponding sediment samples. Nevertheless, the SLERA on the bay sediments revealed that adverse ecological effects to benthic species are expected to occur whereas the HHRA showed that adverse health effects are not expected to occur from the consumption of the mussels.ConclusionsWith the help of a SLERA, it was possible to indicate which class of chlorinated organic compounds is of highest concern to assess and to improve the environmental quality of the bay. Monitoring of organochlorines and chlorpyrifos would be needed to control the future trend of pollution.