Sorption of nano-C60 clusters in soil: hydrophilic or hydrophobic interactions?

We studied the sorption behaviour of fullerene nano-C(60) particles (nC(60)) in soil from binary solvent mixtures of ethanol-water in order to critically evaluate the previous reports in the literature that the partitioning mechanism explains the soil sorption of fullerene C(60) as hydrophobic molecules. The sorption of nC(60) particles was studied in a range of solvent mixtures by changing volume fractions of ethanol from 20 to 100 percent. Sorption and particle characteristics were found to be very different in ethanol : water mixtures above and below 60% ethanol. In the range of 20-60% ethanol, sorption increased from 1.2 to 14.6 L kg(-1) accompanied by a change in zeta (ζ) potential from -32.4 to -7.2 mV. This observation can be attributed to hydrophilic interactions that negatively charged nC(60) particles undergo with soil colloids and water molecules. From 60% to 100% ethanol volume fractions, hydrophobic interactions of weakly charged nanoparticles may control the overall extent of soil sorption. The findings of this study indicate the importance of hydrophilic forces in controlling the sorption behaviour of nC(60) particles which are stabilized in water dominated solvent mixtures. The validity of the partitioning mechanism and K(OC) modelling approach in describing and estimating the sorption of nC(60) particles in soil (previously suggested in the literature) are, therefore, questioned.     

A new nanosilver-based spectrophotometric method for monitoring Eriochrome black T in river water

In this paper, a new spectrophotometric method is reported for the determination of nanomolar levels of Eriochrome black T in environmental samples. The method is based on the catalytic effect of silver nanoparticles on the oxidation of Eriochrome black T by hexacyanoferrate (III) in acetate–acetic acid medium and at 25 °C. The absorbance is measured at 512 nm with the fixed-time method. It relies on the linear relationship between the absorbance difference (?A) and Eriochrome black T amounts in the range of 40–1,250 nM. Under optimum conditions, the sensitivity of the proposed method, i.e., the detection limit corresponding to 80 s, is about 25 nM. The method is featured with good accuracy and reproducibility for Eriochrome black T determination in river water samples without any pre-concentration and separation step.     

Systematic evaluation of dissolved lead sorption losses to particulate syringe filter materials

Distinguishing between soluble and particulate lead in drinking water is useful in understanding the mechanism of lead release and identifying remedial action. Typically, particulate lead is defined as the amount of lead removed by a 0.45-μm filter. Unfortunately, there is little guidance regarding selection of filter membrane material and little consideration to the possibility of the sorption of dissolved lead to the filter. The objective of this work was to examine the tendency of 0.45-μm syringe filter materials to adsorb lead. Tests were performed with water containing 40 and 24 μg/L soluble lead at pH 7 buffered with 50 mg C/L dissolved inorganic concentration (DIC). The amounts of lead sorbed greatly varied by filter, and only two filter types, polypropylene and mixed cellulose esters, performed well and are recommended. Great care must be taken in choosing a filter when filtering soluble lead and interpreting filter results.     

Water chemistry influences the toxicity of silver to the green-lipped mussel Perna viridis

The study determined the influence and relative importance of water chemistry parameters (pH, alkalinity, hardness) on the acute toxicity of silver to the green mussel Perna viridis. A preliminary bioassay revealed that 4 mg L^???1 of silver caused 50% mortality (LC₅₀) in 96 h for mussels placed in seawater with pH 8.5, hardness 1,872 mg L^???1, and alkalinity 172 mg L^???1. Mortality of mussels increased with decreasing pH and increasing hardness and alkalinity variables. In contrast the mortality decreased with increasing pH and decreasing hardness and alkalinity values. The water chemistry also affected the concentration of sliver in experimental seawater and bioaccumulation of silver in mussels. The results revealed that the chemical properties of seawater must be considered while conducting toxicity tests with metals like silver. The possible explanations for the influence of water chemistry on silver toxicity to P. viridis are discussed.     

Methane oxidation and abundance of methane oxidizers in tropical agricultural soil (vertisol) in response to CuO and ZnO nanoparticles contamination

There is worldwide concern over the increase use of nanoparticles (NPs) and their ecotoxicological effect. It is not known if the annual production of tons of industrial nanoparticles (NPs) has the potential to impact terrestrial microbial communities, which are so necessary for ecosystem functioning. Here, we have examined the consequences of adding the NPs particularly the metal oxide (CuO, ZnO) on CH₄ oxidation activity in vertisol and the abundance of heterotrophs, methane oxidizers, and ammonium oxidizers. Soil samples collected from the agricultural field located at Madhya Pradesh, India, were incubated with either CuO and ZnO NPs or ionic heavy metals (CuCl₂, ZnCl₂) separately at 0, 10, and 20 μg g^?1 soil. CH₄ oxidation activity in the soil samples was estimated at 60 and 100 % moisture holding capacity (MHC) in order to link soil moisture regime with impact of NPs. NPs amended to soil were highly toxic for the microbial-mediated CH₄ oxidation, compared with the ionic form. The trend of inhibition was Zn 20?>?Zn 10?>?Cu 20?>?Cu 10. NPs delayed the lag phase of CH₄ oxidation to a maximum of 4-fold and also decreased the apparent rate constant k up to 50 % over control. ANOVA and Pearson correlation analysis (α?=?0.01) revealed significant impact of NPs on the CH₄ oxidation activity and microbial abundance (p?<?0.0001, and high F statistics). Principal component analysis (PCA) revealed that PC1 (metal concentration) rendered 76.06 % of the total variance, while 18.17 % of variance accounted by second component (MHC). Biplot indicated negative impact of NPs on CH₄ oxidation and microbial abundance. Our result also confirmed that higher soil moisture regime alleviates toxicity of NPs and opens new avenues of research to manage ecotoxicity and environmental hazard of NPs.     

Evaluation of Pb (II) biosorption utilizing sugarcane bagasse colonized by <Emphasis Type="Italic">Basidiomycetes</Emphasis>

The contamination of water resources by metallic ions is a serious risk to public health and the environment. Therefore, a great emphasis has been given to alternative biosorption methods that are based on the retention of aqueous-solution pollutants; in the last decades, several agricultural residues have been explored as low-cost adsorbent. In this study, the ability of Pb (II) biosorption using sugarcane bagasse modified by different fungal species was evaluated. The presence of carbonyl, hydroxyl, and carboxyl groups in the biosorbent was observed by spectroscopy in the infrared region. By scanning electron microscopy, changes in the morphology of modified material surfaces were observed. The highest adsorption capacity occurred at pH 5.0, while the shorter adsorbate-adsorbent equilibrium was at 20 min, and the system followed the pseudo-second-order model. The maximum biosorption in isotherms was found at 58.34 mg g^?1 for modified residue by Pleurotus ostreatus U2-11, and the system followed the Langmuir isotherm. The biosorption process was energetically spontaneous with low desorption values. This modification showed great potential for filters to remove Pb (II) and provide the preservation of water resources and animal health.     

A nanosilver-based spectrophotometric method for determination of malachite green in surface water samples

A new spectrophotometric method is reported for the determination of nanomolar level of malachite green in surface water samples. The method is based on the catalytic effect of silver nanoparticles on the oxidation of malachite green by hexacyanoferrate (III) in acetate–acetic acid medium. The absorbance is measured at 610 nm with the fixed-time method. Under the optimum conditions, the linear range was 8.0?×?10^?9–2.0?×?10^?7?mol?L^?1 malachite green with a correlation coefficient of 0.996. The limit of detection (S/N?=?3) was 2.0?×?10^?9?mol?L^?1. Relative standard deviation for ten replicate determinations of 1.0?×?10^?8?mol?L^?1 malachite green was 1.86 %. The method is featured with good accuracy and reproducibility for malachite green determination in surface water samples without any pre-concentration and separation step.     

Impacts of intensive agricultural irrigation and livestock farming on a semi-arid Mediterranean catchment

Irrigation return flows (IRF) are a major contributor of non-point source pollution to surface and groundwater. We evaluated the effects of irrigation on stream hydrochemistry in a Mediterranean semi-arid catchment (Flumen River, NE Spain). The Flumen River was separated into two zones based on the intensity of irrigation activities in the watershed. General linear models were used to compare the two zones. Relevant covariables (urban sewage, pig farming, and gypsum deposits in the basin) were quantified with the help of geographic information system techniques, accompanied by ground-truthing. High variability of the water quality parameters and temporal dynamics caused by irrigation were used to distinguish the two river reaches. Urban activity and livestock farming had a significant effect on water chemistry. An increase in the concentration of salts (240–541 μS·cm^???1 more in winter) and nitrate (average concentrations increased from 8.5 to 20.8 mg·l^???1 during irrigation months) was associated with a higher level of IRF. Those river reaches more strongly influenced by urban areas tended to have higher phosphorus (0.19–0.42 mg·l^???1 more in winter) concentrations. These results support earlier research about the significant consequences to water quality of both urban expansion and intensive agricultural production in arid and semi-arid regions. Data also indicate that salinization of soils, subsoils, surface water, and groundwater can be an unwelcome result of the application of pig manure for fertilization (increase in sodium concentration in 77.9 to 138.6 mg·l^???1).     

Influence of formulation on mobility of metazachlor in soil

The mobility of metazachlor [2-chloro-N-(pyrazol-1-ylmethyl)acet-2′,6′-xylidide] in sand soil and loamy sand soil was studied in a soil column under laboratory conditions. Commercial metazachlor formulation (Metazachlor 500 suspension concentrate (SC)) and metazachlor immobilized in alginate matrix were used for leaching experiment. The initial concentration of metazachlor in soil for both formulations was 2.0 mg mL^?1. After application of herbicide, the columns were irrigated with 100, 40, and 3.7 mm of water. After 1 h, when addition of water was completed, soils were sampled in 5-cm segments and were used for the analysis of residues. The use of alginate controlled release (CR) formulation reduced the vertical mobility of metazachlor into soil layer in comparison with the formulation SC.     

Analysis of urban effects on soil temperature in Ankara

In this study, data from two different meteorology stations were analyzed in order to reveal the effects of the urbanization on the soil temperature. These stations are the Ankara Meteorology Station (AMS), showing the urban effects, and the Esenbo?a Meteorology Station (EMS), showing the rural effects. The soil temperatures measured at depths of 5, 10, 20, and 50 cm at 0700, 1400, and 2100 hours between 1960 and 2005 were used in the analysis. Long-term mean monthly temperatures at each depth and at each time considered were calculated and analyzed using Sen’s slope and Mann–Kendall tests. The results showed that the mean monthly urban soil temperatures were generally higher than the rural soil temperatures. The differences between temperatures measured at 5, 10, 20, and 50 cm in urban and rural stations (ΔT _s(AMS???EMS)) ranged between 1.8°C and 2.1°C. As in the urban heat islands, the differences between the urban and rural soil temperatures are high at 2100 hours and low at 1400 hours. It was also observed that, due to the increasing number of buildings around the Esenbo?a Station in recent years, the difference between the urban and rural soil temperatures seems to have become smaller. These show that the factors affecting the urban heat islands and those affecting the soil temperatures are similar. Also, the temperature differences were observed to be higher during the warm season than in the cold season. The frequency distributions of the temperature differences (ΔT _s(AMS???EMS)) reveal both positive and negative values. However, the positive temperature differences are obviously prevalent.     

Evaluation of ozonation technique for pesticide residue removal and its effect on ascorbic acid,cyanidin-3-glucoside,and polyphenols in apple (<Emphasis Type="Italic">Malus domesticus</Emphasis>) fruits

Ozonated water dip technique was evaluated for the detoxification of six pesticides, i.e., chlorpyrifos, cypermethrin, azoxystrobin, hexaconazole, methyl parathion, and chlorothalonil from apple fruits. Results revealed that ozonation was better than washing alone. Ozonation for 15 min decreased residues of the test pesticides in the range of from 26.91 to 73.58%, while ozonation for 30 min could remove the pesticide residues by 39.39–95.14 % compared to 19.05–72.80 % by washing. Cypermethrin was the least removed pesticide by washing as well as by ozonation. Chlorothalonil, chlorpyrifos, and azoxystrobin were removed up to 71.45–95.14 % in a 30-min ozonation period. In case of methyl parathion removal, no extra advantage could be obtained by ozonation. The HPLC analysis indicated that ozonation also affected adversely the ascorbic acid and cyanidin-3-glucoside content of apples. However, 11 polyphenols studied showed a mixed trend. Gallic acid, 3,4-dihydroxybenzoic acid, catechin, epicatechin, p-coumaric acid, quercetin-3-O-glucoside, quercetin, and kaempferol were found to decrease while syringic acid, rutin, and resveratrol were found to increase in 30-min ozonation.     

A complex investigation of the extent of pollution in sediments of the Sava River: part 2: persistent organic pollutants

Sediment pollution of the biggest Danube tributary, the Sava River, was investigated within the sixth framework European Union project “Sava River Basin: Sustainable Use, Management and Protection of Resources” (SARIB). The extent of pollution was estimated by determining the amount of inorganic and persistent organic pollutants in sediment samples at 20 selected sampling sites along the Sava River. For the purpose of clarity, the findings are presented and published separately (part I: selected elements and part II: persistent organic pollutants). This study presents an investigation into the presence of organic pollutants in the Sava River sediment. According to the Water Framework Directive, the following persistent organic pollutants were investigated: polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenyls (PCB), selected chlorinated pesticides and organotin compounds. The results reveal that PAHs were present in moderate concentrations (sum of 16 PAHs: up to 4,000 ng g^???1) and their concentrations increased downstream. Concen trations of PCB were low (sum of seven indicator PCBs: below 4 ng g^???1) and among the pesticides analyzed only p,p-dichlorodiphenyltrichloroethane was found in moderate concentrations at two sampling sites in Croatia (up to 3 ng g^???1) and hexachlorobenzene was found in a high concentration in the city of Belgrade (91 ng g^???1), although the use of these persistent pesticides has been banned for decades. Repeated sampling at the same location revealed point pollution near Belgrade. Among the organic pollutants surveyed, organotin compounds were not detected. Overall results reveal the presence of persistent organic pollutants in 20 of the Sava River sediments tested that is, in general, comparable or lower than the levels in the Danube River and other moderately polluted European rivers.     

Planted floating bed performance in treatment of eutrophic river water

The objective of the study was to treat eutrophic river water using floating beds and to identify ideal plant species for design of floating beds. Four parallel pilot-scale units were established and vegetated with Canna indica (U1), Accords calamus (U2), Cyperus alternifolius (U3), and Vetiveria zizanioides (U4), respectively, to treat eutrophic river water. The floating bed was made of polyethylene foam, and plants were vegetated on it. Results suggest that the floating bed is a viable alternative for treating eutrophic river water, especially for inhibiting algae growth. When the influent chemical oxygen demand (COD) varied from 6.53 to 18.45 mg/L, total nitrogen (TN) from 6.82 to 12.25 mg/L, total phosphorus (TP) from 0.65 to 1.64 mg/L, and Chla from 6.22 to 66.46 g/m³, the removal of COD, TN, TP, and Chla was 15.3 %–38.4 %, 25.4 %–48.4 %, 16.1 %–42.1 %, and 29.9 %–88.1 %, respectively. Ranked by removal performance, U1 was best, followed by U2, U3, and U4. In the floating bed, more than 60 % TN and TP were removed by sedimentation; plant uptake was quantitatively of low importance with an average removal of 20.2 % of TN and 29.4 % of TP removed. The loss of TN (TP) was of the least importance. Compared with the other three, U1 exhibited better dissolved oxygen (DO) gradient distributions, higher DO levels, higher hydraulic efficiency, and a higher percentage of nutrient removal attributable to plant uptake; in addition, plant development and the volume of nutrient storage in the C. indica tissues outperformed the other three species. C. indica thus could be selected when designing floating beds for the Three Gorges Reservoir region of P. R. China.     

Bacteriological safety assessment,hygienic habits and cross-contamination risks in a Nigerian urban sample of household kitchen environment

Urban household kitchen environment was assessed for safety by determining their levels of indicator bacteria, hygienic habits and risk of cross-contamination. Household kitchens (60) were selected in Warri Town, Nigeria, by the multi-stage sampling technique. Contact surfaces, water and indoor kitchen air were analysed for aerobic plate counts, total and faecal coliforms using Nutrient and McConkey media by swab/rinse method, membrane filtration and sedimentation methods, respectively. Hygienic habits and risk of cross-contamination were assessed with structured questionnaire which included socio-demographic variables. On the basis of median counts, the prevalence of high counts (log cfu/cm²/m³/100 mL) of aerobic plate counts (>3.0), total coliforms (>1.0) and faecal coliforms (>0) on contact surfaces and air was high (58.0–92.0%), but low in water (30.0–40.0%). Pots, plates and cutleries were the contact surfaces with low counts. Prevalence of poor hygienic habits and high risk of cross-contamination was 38.6 and 67.5%, respectively. Education, occupation and kitchen type were associated with cross-contamination risk (P = 0.002–0.022), while only education was associated with hygienic habits (P = 0.03). Cross-contamination risk was related (P = 0.01–0.05) to aerobic plate counts (OR 2.30; CL 1.30–3.17), total coliforms (OR 5.63; CL 2.76–8.25) and faecal coliforms (OR 4.24; CL 2.87–6.24), while hygienic habit was not. It can be concluded that urban household kitchens in the Nigerian setting are vulnerable to pathogens likely to cause food-borne infections.     

Spectrophotometric determination of anionic surfactants: optimization by response surface methodology and application to Algiers bay wastewater

A simple analytical method for quantitative determination of an anionic surfactant in aqueous solutions without liquid-liquid extraction is described. The method is based on the formation of a green-colored ion associate between sodium dodecylbenzenesulfonate (SDBS) and cationic dye, Brilliant Green (BG) in acidic medium. Spectral changes of the dye by addition of SDBS are studied by visible spectrophotometry at maximum wave length of 627 nm. The interactions and micellar properties of SDBS and cationic dye are also investigated using surface tension method. The pH, the molar ratio ([BG]/[SDBS]), and the shaking time of the solutions are considered as the main parameters which affect the formation of the ion pair. Determination of AS in distilled water gives a significant detection limit up to 3?×?10^?6?M. The response surface methodology (RSM) is applied to study the absorbance. A Box-Behnken is a model designed to the establishment of responses given by parameters with great probability. This model is set up by using the three main parameters at three levels. Analysis of variance shows that only two parameters affect the absorbance of the ion pair. The statistical results obtained are interesting and give us real possibility to reach optimum conditions for the formation of the ion pair. As the proposed method is free from interferences from major constituents of water, it has been successfully applied to the determination of anionic surfactant contents in wastewaters samples collected from Algiers bay.     

Alteration of antioxidant enzymes and impairment of DNA in the SiO2 nanoparticles exposed zebra fish (Danio rerio)

The incorporation of nanoparticles in industrial and biomedical applications has increased significantly in recent years, yet their hazardous and toxic effects have not been studied extensively. While standard toxicological test methods are generally capable of detecting the toxic effects, the choice of relevant methods for nanomaterials is still discussed. Among the various oxide nanomaterials, silica nanoparticles are widely used in biological applications that include nano-medicine. But studies on adverse effects of silica nanoparticle exposure to fish remain unclear. Therefore, the present study was designed to investigate the oxidative toxic effects of silicon dioxide nanoparticles using fish model. The size of the SiO₂ nanoparticles was between 68 and 100 nm which was confirmed by X-ray diffractometer, dynamic light scattering, scanning electron microscope and transmission electron microscope. The zebra fish were exposed to sub-lethal concentrations (5 and 2.5 mg/L) of characterized SiO₂ nanoparticles for a period of 7 days. After 7 days, SiO₂ nanoparticle-treated fishes were sacrificed, and tissues such as liver, muscle and gill were dissected out for the analysis of antioxidant enzymes and DNA fragmentation. The DNA profiles were analysed in the tissues of zebra fish that treated with SiO₂ nanoparticles. Tissues of fish from clean water were used as control, and DNA profiles were analysed. It is found that DNA from control tissues was intact, whereas the tissues treated with SiO₂ were all fragmented. SiO₂ nanoparticle-mediated antioxidant enzymes activities, such as catalase, superoxide dismutase, glutathione (GSH)-S-transferase, glutathione reductase and GSH, in the tissues of zebra fish were measured. The results revealed that alteration of antioxidant enzymes due to SiO₂ nanoparticle can be considered as a biomarker to SiO₂-mediated oxidative stress in biological samples.     

Assessment of elemental concentrations in the urban air (case study: Tehran city)

Tehran is one of the megacities of the world with a population of over eight million. Its air is highly polluted mainly due to the suspended particulate matters, which encompasses a wide spectrum of chemical elements. These elements based on their type, size, and impact on the life cycle have various environmental and heath risks. In this research, the neutron activation method is used to determine the concentration levels of Al, Ba, Fe, Mg, and V in the urban air. Thus, two districts of Tehran with different characteristics are selected. District 21 includes much of the industries located in Tehran metropolitan and is considered as an industrial area. In contrast, district 22 lacks any significant industrial activity. It is a newly established and expanding district adjacent to district 21 with a great deal of constructional activities. For the measurement of the suspended particulate matters in the air, the various sections of the aforesaid districts with industrial, residential, heavily congested traffic, residential/commercial, residential/heavily congested traffic, and residential/industrial classifications were identified. Subsequently, 24 sampling stations were selected. The sampling of the suspended particulate matters was conducted with the aid of a high volume pump containing 125 mm cellulose filters in two different time intervals. After completion of the sampling process, the samples were prepared and sent to the research reactor of the Iran Nuclear Energy Organization for Neutron Activation. During the next steps, the radiations emitted from the samples were registered, the radiation curves were plotted, and the amounts of the trace elements were determined. As a result, the average concentration levels of Al, Ba, Fe, Mg, and V were identified to be 3.301140, 2.273658 × 10, 4.0681696 × 10^???1, 3.5525475 × 10^???1, and 3.04075 × 10^???2 μg/m³, respectively. Moreover, the emission sources of the aforesaid elements into the air were identified. The concentration levels of these elements in the industrial and heavily congested traffic sections were higher. Finally, it was concluded that the statistical analysis of these elements presents a meaningful correlation among them.     

葫芦脲聚合膜的制备及其在水体被动采样技术中的应用

基于葫芦脲的超分子特性,以醋酸纤维素为载体,制备了葫芦脲膜,采用傅里叶红外光谱、扫描电镜、热重分析对膜的性能进行了表征,研究了葫芦脲膜对三氯生(TCS)和三氯卡班(TCC)的吸附性能,验证了以葫芦脲膜为结合相的被动采样技术测定2种物质的可行性。结果表明:葫芦脲分子确实被引入到醋酸纤维素中,相比于醋酸纤维素膜,葫芦脲膜具有更强的热稳定性和吸附性能;以葫芦脲膜为结合相的被动采样装置在不同环境因素(pH值、离子强度、可溶性有机质)下都具有良好的工作稳定性;将该装置布设到南京市秦淮河中的2个采样点,野外实验验证了该采样装置应用于监测实际水体中的TCS和TCC的可行性。     

Environmental applications of poly(amic acid)-based nanomaterials

Nanoscale materials offer new possibilities for the development of novel remediation and environmental monitoring technologies. Different nanoscale materials have been exploited for preventing environmental degradation and pollutant transformation. However, the rapid self-aggregation of nanoparticles or their association with suspended solids or sediments where they could bioaccumulate supports the need for polymeric coatings to improve mobility, allows faster site cleanups and reduces remediation cost. The ideal material must be able to coordinate different nanomaterials functionalities and exhibit the potential for reusability. We hereby describe two novel environmental applications of nanostructured poly (amic acid)-based (nPAA) materials. In the first application, nPAA was used as both reductant and stabilizer during the in situ chemical reduction of chromium(vi) to chromium(iii). Results showed that Cr(vi) species were rapidly reduced within the concentration range of 10(-1) to 10(2) mM with efficiency of 99.9% at 40 °C in water samples and 90% at 40 °C in soil samples respectively. Furthermore, the presence of PdNPs on the PAA-Au electrode was found to significantly enhance the rate of reduction. In the second application, nPAA membranes were tested as filters to capture, isolate and detect nanosilver. Preliminary results demonstrate the capability of the nPAA membranes to quantitatively capture nanoparticles from suspension and quantify their abundance on the membranes. Silver nanoparticles detection at concentrations near the toxic threshold of silver was also demonstrated.     

Environmental monitoring of linear alkylbenzene sulfonates and physicochemical characteristics of seawater in El-Mex Bay (Alexandria, Egypt)

In the present work, the influence of different physicochemical characteristics on the distribution of anionic detergents, linear alkylbenzene sulfonates (LAS), was studied. Surface and bottom water samples were collected from eight different sites from a small bay near the main sewage discharge of Alexandria City (El-Max Bay). The results showed great variations in the concentrations, as a function of the regional and seasonal variations. The study revealed that the pH values lie in the normal side, with a range of 8.0–8.5 inside the bay and 7.5–7.7 at El-Umum Drain effluent. Wide variations, observed between the surface and the bottom water of the bay, salinity, dissolved oxygen, oxidizable organic matter, total hardness, and total alkalinity, were scattered in the ranges (3.33–42.73 practical salinity unit), (0.42–8.27 mg O₂/l), (0.12–10.49 mg/l), (1.39–8.99 mg/l), and (0.23–0.48 mg/l), respectively. The regional variations of LAS concentrations in the bay waters showed that the concentration decreased as the distance from the source of drainage water (El-Umum Drain). The seasonal average variations of LAS cleared out that summer and spring periods had the highest concentrations at surface (0.13?±?0.04 mg LAS/l) and bottom (0.12?±?0.10 mg LAS/l) layer, which is attributed to increase in population density and human activities. The inverse relationships between total LAS concentration and salinity, dissolved oxygen, and calcium ions concentration are r?=??0.78, 0.50, and 0.67, respectively. This is related to the occurrence of the untreated wastewater containing detergents, the biodegradation rate of surfactants, and strong precipitation of LAS as Ca.