Interrelationship between geochemical elements of sediment and groundwater at Samrak Park Delta of Nakdong River Basin in Korea: multivariate statistical analyses and artificial neural network approaches

This research was conducted at Samrak Park Delta of Nakdong River Basin in Busan Metropolitan City, Korea. The main objective of this study was to evaluate the interrelationship of geochemical elements in sediments and groundwater through multivariate statistical analyses and a multilayer perceptron artificial neural network model. The mean concentrations of chemical elements were Si (46%), Fe (16.9%), Al (15.7%), K (7.5%) and Ca (4.5%) in sediments, and Na (8650 mg/L), Mg (999 mg/L), Ca (432 mg/L), K (293 mg/L) and Cl (17,640 mg/L) in groundwater, respectively. The principal component analysis produced 3 kinds of factors with the variances of 63.37, 27.02 and 9.62%, respectively. It is suggested that the chemical components of sediments and groundwater were mainly originated from source rocks and seawater intrusion, with the minor impacts of irrigation and industry. Cluster analysis also showed that chemical elements were mainly controlled by the natural geogenic sources and seawater intrusion. Multilayer perceptron of artificial neural network (ANN) presented the good interrelationship between sediment and groundwater. The determination coefficients (R ²) between ANN predicted values and observed values in groundwater showed the high values of 0.61–0.97 except Mg, Mn and Sr. It is revealed that the chemical components of sediment and groundwater were derived from local geological origin and from the minor impact of anthropogenic sources. Multivariate analyses and ANN contributed to the identification of the mutual relationship between the geochemical elements of sediment and those of groundwater.     

Numerical modeling of brine disposal from Gaza central seawater desalination plant

Gaza central seawater desalination plant is a promising solution to alleviate the problem of water crisis in the Gaza Strip. The plant in the short term, phase (I), will desalinate seawater for potable uses with a capacity of 55 million cubic meters per year, while in the long term, phase (II), the plant capacity will be doubled to 110 million cubic meters per year of freshwater. As a product from the reverse osmosis process, a huge amount of brine with salinity reaches to 75,000 mg/L will be redirected to seawater; nearly 12,200 m³/h of brine will be rejected from phase (I) while in the long term, a brine flow rate of 24,400 m³/h will be disposed from phase (II). In order to minimize the negative impacts of the rejected brine on the marine environment, it is urgent to modeling numerically the impact of the discharged brine through various disposal systems to define the most environmental system. Various scenarios were defined and simulated using CORMIX model to study the efficiencies of onshore surface open channel, offshore submerged single port as well as offshore submerged multiport outfalls taking salinity variations as an indicator. Sensitivity analysis was conducted to identify the most influencing input parameters on the simulation results as well as to evaluate the optimal environmental disposal system which can mitigate the adverse impacts of brine on the marine ecosystem as much as possible in the worst seawater conditions. The simulation results showed that the discharge via surface open channel is not environmentally feasible where the seawater salinity rose by more than 2000 mg/L at RMZ. The single-port scenario can meet the regulations at RMZ but the standard at GMZ was not met, where the rejected brine from phase (I) through single port at 1500 m offshore raises the seawater salinity at GMZ by more than 600  mg/L. The staged multiport outfall, capped by 24 ports, achieves acceptable brine dilution at seawater depth of about 7.5  m, and in the worst ambient conditions in the case of phase (II) in operation, the brine’s excess salinity was 536, 497, and 379 mg/L above the salinity of seawater at RMZ, GMZ, and ROI, respectively.     

Determination of radioactivity levels in Akhisar,Gördes,Gölmarmara and Sindirgi regions,Western Turkey

In this study, radioactivity measurements in the environment of Akhisar, Gölmarmara, Gördes and Sindirgi regions in Western Turkey were investigated in order to evaluate the implications of any excess radioactivity in the environment of geological formation. The radioactivity concentrations of ⁴⁰K, ²³⁸U and ²³²Th radionuclides in the soil samples were measured by a NaI(Tl) gamma spectrometer system, and the radium activity concentrations in the water samples were also analyzed by an ZnS(Ag) alpha counter by the collector chamber method. The radioactivity of ⁴⁰K, ²³⁸U and ²³²Th in soils ranged 2.80–2,347.77, 9.90–256.19 and 9.66–106.53 Bq kg^?1, respectively. The activity of ²²⁶Ra in the water samples ranged from 0.03 Bq L^?1 (0.89pCi/L) to 0.80 Bq L^?1 (21.58pCi/L). In addition, the external terrestrial gamma dose rate in air (nGy h^?1), annual effective dose rate (mSv year^?1) and radium equivalent activity (Bq kg^?1) were calculated and compared with international standard values.     

Role of Suspended Particulate Matter in Regulating the Behavior of Dissolved Uranium in the Yellow River Estuary

In order to examine the mixing behavior of dissolved uranium (U) in estuaries under different suspended particulate matter (SPM) regimes, three laboratory-based experiments were conducted by mixing seawater with river water containing different concentrations of SPM. Comparing this study with other field and laboratory-based experiments, dissolved U behaved differently depending upon the concentration of SPM. When SPM concentrations are >?0.8 g/L in the Yellow River, desorption/dissolution of U from SPM becomes predominant and dissolved U is enriched relative to the theoretical mixing line. However, when SPM concentrations are <?0.8 g/L, dissolved U behaves conservatively with some extent of removal during estuarine mixing. ²³⁴U/²³⁸U activity ratios were somewhat constant showing no measurable isotopic fractionation during physical mixing and U sorption/desorption to/from particles. Addition of dissolved ²³⁸U desorbed/dissolved from SPM during the annual Yellow River water-sediment regulation scheme (Jun 30th–Jul 14th, 2014) was estimated at 6.4?×?10¹¹ dpm, about 9% of the total riverine flux of dissolved ²³⁸U during that same period. This study represents a contribution to studies of dissolved U in muddy rivers and estuaries throughout the world. Results reported here provide not only a perspective to better estimate U flux from rivers to the ocean but also new insights into better understanding its estuarine mixing behavior and controlling factors.     

Natural radionuclide concentrations in thermal springs of east Algeria

The variation of the natural radionuclide concentrations depends on the chemical composition of each site. In this work, two thermal springs in the east of Algeria have been chosen to assess the activity concentration of natural radionuclide, mainly the three natural radioactive series ²³⁸U, ²³⁵U and ²³²Th, and ⁴⁰K. The high-resolution gamma ray spectroscopy was used to determine these concentrations. In these water samples, ²³⁵U, ²³⁴Th, ²¹⁰Pb, ²²⁶Ra radionuclides are less than the minimum detectable activity. The activity of ²³⁸U is dominant. The ²³⁸U activity was determined by taking the mean activity of two separate photo-peaks of daughter nuclides ²¹⁴Pb at 351.92 (37.2%) keV and ²¹⁴Bi at 609.31 (45%) keV. The measured activity concentrations of ²³⁸U in water samples obtained from the concentrations of ²¹⁴Bi and ²¹⁴Pb ranged from 0.56 ± 0.20 to 1.13 ± 0.20 Bq/L. The annual effective dose value due to the ingestion of the measured radionuclide ²³⁸U in 1 L of water, for an adult, ranged from 9.20 to 18.56 µSv.     

Calcite and aragonite saturation States of Kamaran strait surface seawater, Yemen: summer time

Surface seawater samples from Kamaran Strait of Yemen were collected for physical and chemical parameter determinations. This work reports the results of air and surface seawater temperature, salinity, pH, and total alkalinity measurements. The air temperature ranged from 29.9°C to 36.5°C with an average value of 31.5?±?1.5°C, whereas the seawater surface temperature ranged from 34.0°C to 36.0°C with a mean value of 34.5?±?0.5°C. The salinity was observed to be high, ranging from 38.03 to 38.81 with an average value of 38.45?±?0.22. The pH ranged from 7.74 to 8.27 with a mean value of 8.11?±?0.10. The total alkalinity was found to range from 2.3860 to 2.5000 meq L^?1 with an average value of 2.4288?±?0.0351 meq L^?1. The result of the study showed that there was a negative correlation between the pH and surface seawater temperature and salinity. The surface seawater of the Kamaran Strait was found to be several fold supersaturated with respect to calcium carbonate. The measured percent degree of saturation ranged from 454% to 668% with respect to calcite and from 246% to 361% with respect to aragonite. The lowest value of supersaturation with respect to both calcite and aragonite were found in front of as-Salif port, where human and developmental activities are intensively increased. The visual inspection of coral reefs distribution and their intensity were obviously observed in areas of high value of supersaturation with respect to both minerals, high transparency of seawater column, and low human activities. Further studies are needed to investigate the occurrence, distribution, and mineralogy of corals and the effects of physical and chemical parameters upon their growth in the region.     

Anomalous concentrations of radionuclides in the groundwater of Ede area,southwestern Nigeria: a direct impact of geology

An assessment of the groundwater in areas underlain by pegmatite in Ede, southwestern Nigeria was carried out to determine the concentration of Potassium-40 (⁴⁰K), Uranium-238 (²³⁸U) and Thorium-232 (²³²Th) radionuclides. In the earlier work, it was established that zircons in these pegmatites have suffered a high degree of metamictization that has enhanced continuous loss of some radionuclides since the time of emplacement of the pegmatite host rock to the present. The aim of this work is to determine whether or not there is corresponding increase in the concentration of radionuclides in groundwater in the study area. Fifteen groundwater samples were collected from both hand dug wells and boreholes in the area. Ten samples were from Ede town, two samples each from nearby communities of Iddo and Ekuro and one from Iwoye, where the bedrocks were not pegmatites. All the 15 samples were analyzed with the Sodium Iodide scintillator (NaI [Tl]) detector at the Centre for Energy Research and Development, Obafemi Awolowo University, Ile-Ife, Nigeria. The results showed varying concentrations of the radionuclides in the water samples. Activity concentrations of Potassium-40 (⁴⁰K) indicated an average value of 17.149 Bq/L for samples from Ede, 9.265 Bq/L for Iddo, 6.6 Bq/L for Ekuro, while Iwoye has a value of 21.21 Bq/L. The Uranium-238 (²³⁸U) series had an average value of 13.64 Bq/L for Ede, 13.49 Bq/L for Ekuro, 11.685 Bq/L for Iddo and 12.04 Bq/L for the lone sample from Iwoye. Thorium-232 (²³²Th) series had an average value of 11.182 Bq/L for Ede, while average values of 7.79 Bq/L and 9.025 Bq/L, respectively, were recorded for Iddo and Ekuro and 12.25 Bq/L for Iwoye. The annual effective dose level of ⁴⁰K is generally below the World Health Organization (WHO) recommended dosage of 0.1 mSv/y except for three locations, while those of ²³⁸U and ²³²Th are in excess of the standard values. The high radionuclides in the groundwater in the study area were not due to anthropogenic sources but directly due to geological processes which release the radioisotopes from rocks after weathering, continuous loss from metamict minerals and natural lateral mobility from regions of radionuclides’ release to other areas. There is thus the need to carry out systematic studies of the radionuclides concentrations on regional scale in the area which could lead to investigating on both short- and long-term health effects on organic species in these areas, and development of purification systems before utilizing water from the areas for domestic and industrial purposes.     

Optimization of parameters using response surface methodology and genetic algorithm for biological denitrification of wastewater

In the present study the removal of nitrates from wastewater using Pseudomonas stutzeri microorganism in a Gas–Liquid–Solid bioreactor at the concentration of 200 ppm was studied for a period of 12 h. The response surface methodology with the help of central composite design and genetic algorithm were employed to optimize the process parameters such as airflow rate, biofilm carrier, carbon source, temperature and pH which are responsible for the removal of nitrates. The optimized values of parameters found from RSM are airflow rate 2.41 lpm, biofilm carrier 15.15 g/L, carbon source 85.0 mg/L, temperature 29.74 °C, pH 7.47 and nitrate removal 193.16. The optimized parameters obtained from genetic algorithm are airflow rate 2.42 lpm, biofilm carrier 15.25 g/L, carbon source 84.98 mg/L, temperature 29.61 °C, pH 7.51 and nitrate removal is 194.14. The value of R² > 0.9831 obtained for the present mathematical model indicates the high correlation between observed and predicted values. The optimal values for nitrate removal at 200 ppm are suggested according to genetic algorithm and at these optimized parameters more than 96 % of nitrate removal was estimated, which meets the standards for drinking water.     

Fluoride contamination of groundwater in parts of eastern India and a preliminary experimental study of fluoride adsorption by natural haematite iron ore and synthetic magnetite

Incidence of high fluoride (F^?) in groundwater (>1.5 mg/L) in two tribal belts of eastern India, one around Chukru in the Palamau district of Jharkhand and the other around Karlakot in the Nuapada district of Odisha, has been studied. The maximum concentration of F^? in groundwater from dug wells and tube wells is 10.30 mg/L in Chukru and 4.62 mg/L in Karlakot. The groundwaters are mildly alkaline with pH ranges of 7.52–8.22 and 7.33–8.20 in Chukru and Karlakot, respectively. The F^? concentration is positively correlated with pH, electrical conductivity and SO₄ ^2? in both areas. The high F^? in groundwater resulted mainly from dissolution of biotite and fluorapatite in quartzofeldspathic gneiss. The ionic dominance pattern (in meq/L) is mostly in the order Ca²⁺ > Na⁺ > Mg²⁺ > K⁺ among cations and HCO₃ ^? > SO₄ ^2? > < Cl^? > F^? among anions in the Karlakot groundwater. Preliminary adsorption experiments were conducted on natural haematite iron ore and synthetic magnetite to evaluate their potential for F^? removal from water. Effects of different parameters such as contact time, pH, adsorbent dose and initial F^? concentration on the adsorption capacity of these materials were investigated. Strong dependence of F^? removal on pH was observed for both the adsorbents. With natural haematite iron ore, the maximum F^? removal of 66 % occurred at an initial pH of 3.2 for a solution with F^? concentration of 3 mg/L, adsorbent dose of 7 g/L and overnight contact time. The haematite iron ore was observed to increase the pH of the F^? solution. Adsorption equilibrium was not achieved with this adsorbent even after a contact time of 45.2 h. In the case of synthetic magnetite, 84 % F^? removal was achieved after 2 min of contact time for a solution with F^? concentration of 6 mg/L, adsorbent dose of 10 g/L and initial pH of 7. The results indicate high potential of both natural haematite iron ore and synthetic magnetite as adsorbents of F^? in water.     

Salinization of porewater in a multiple aquitard-aquifer system in Jiangsu coastal plain,China

Chemical and isotopic compositions were analyzed in porewater squeezed from a clayey aquitard in Jiangsu coastal plain, eastern China, to interpret the salinity origin, chemical evolution and water-mass mixing process. A strong geochemical fingerprint was obtained with an aligned Cl/Br ratio of 154 in the salinized aquitard porewater over a wide Cl^? concentration range (396–9,720 mg/L), indicating that porewater salinity is likely derived from a mixing with old brine with a proportion of less than 20%. Very small contributions of brine exerted limited effects on water stable isotopes. The relationships between porewater δ¹⁸O and δD indicate that shallow and intermediate porewaters could be original seawater and were subsequently diluted with modern meteoric water, whereas deep porewaters with depleted stable isotopic values were probably recharged during a cooler period and modified by evaporation and seawater infiltration. The cation–Cl relationship and mineralogy of associated strata indicate that porewater has been chemically modified by silicate weathering and ion-exchange reactions. ⁸⁷Sr/⁸⁶Sr ratios of 0.7094–0.7112 further confirm the input source of silicate minerals. Numerical simulations were used to evaluate the long-term salinity evolution of the deep porewater. The alternations of boundary conditions (i.e., the third aquifer mixed with brine at approximately 70 ka BP, followed by recharge of glacial meltwater at 20–25 ka BP, and then mixing with Holocene seawater at 7–10 ka BP) are responsible for the shift in porewater salinity. These timeframes correspond with the results of previous studies on ancient marine transgression-regression in Jiangsu coastal plain.     

Assessment of natural radioactivity,associated radiological health hazards indices and soil-to-crop transfer factors in cultivated area around a fertilizer factory in Onne,Nigeria

Concentration of natural radionuclides in three major staple food crops cultivated around a fertilizer plant in Onne, Rivers State Nigeria and the cultivated soil samples were determined using gamma spectroscopy operated on a Canberra vertical high purity 3″ × 3″ NaI(TI) detector. The average activity concentration of ²³⁸U, ²³²Th and ⁴⁰K was determined, for cassava flour (U 19.3 ± 5.0, Th 11.4 ± 3.3, K 426.9 ± 33.8) Bq kg^?1, for yam flour (U 6.3 ± 1.8, Th 8.4 ± 2.6, K 227.0.9 ± 27.3) Bq kg^?1 while for cocoyam flour (U 7.5 ± 2.7, Th 7.1 ± 2.3, K 195.8 ± 25.83) Bq kg^?1. The mean activity concentration for soil samples is 18.7 ± 3.7 Bq kg^?1, 18.0 ± 3.8 Bq kg^?1 and 308.4 ± 22.4 Bq kg^?1 for ²³⁸U, ²³²Th and ⁴⁰K, respectively. These values obtained show enhanced ⁴⁰K concentration which is attributed to the effluent discharge from a fertilizer plant and its applications to farmlands, but ²³⁸U, ²³²Th values are well within the global average and values reported in some regions and countries of the world. Radiation hazard indices obtained to estimate potential radiological health risk in both foodstuffs and soil samples are well below their permissible limit as set by UNSCEAR [Sources and effects of ionizing radiation (Report to the General Assembly), 2000]. The rate of radionuclides transfer from soil to crops was moderate with mean transfer factors of ²³²Th < ²³⁸U < ⁴⁰K.     

Mechanism of fluoride enrichment in groundwater of hard rock aquifers in Medak,Telangana State,South India

A total of 194 groundwater samples were collected from wells in hard rock aquifers of the Medak district, South India, to assess the distribution of fluoride in groundwater and to determine whether this chemical constituent was likely to be causing adverse health effects on groundwater user in the region. The study revealed that the fluoride concentration in groundwater ranged between 0.2 and 7.4 mg/L with an average concentration of 2.7 mg/L. About 57% of groundwater tested has fluoride concentrations more than the maximum permissible limit of 1.5 mg/L. The highest concentrations of fluoride were measured in groundwater in the north-eastern part of the Medak region especially in the Siddipeta, Chinnakodur, Nanganoor and Dubhaka regions. The areas are underlain by granites which contain fluoride-bearing minerals like apatite and biotite. Due to water–rock interactions, the fluoride has become enriched in groundwater due to the weathering and leaching of fluoride-bearing minerals. The pH and bicarbonate concentrations of the groundwater are varied from 6.6 to 8.8 and 18 to 527 mg/L, respectively. High fluoride concentration in the groundwater of the study area is observed when pH and the bicarbonate concentration are high. Data plotted in Gibbs diagram show that all groundwater samples fall under rock weathering dominance group with a trend towards the evaporation dominance category. An assessment of the chemical composition of groundwater reveals that most of the groundwater samples have compositions of Ca²⁺–Mg²⁺–Cl^? > Ca²⁺–Na⁺–HCO₃ ^? > Ca²⁺–HCO₃ ^? > Na⁺–HCO₃ ^?. This suggests that the characteristics of the groundwater flow regime, long residence time and the extent of groundwater interaction with rocks are the major factors that influence the concentration of fluoride. It is advised not to utilize the groundwater for drinking purpose in the areas delineated, and they should depend on alternate safe source.     

The distribution of nitrogen speciation and sources of nitrate in the north of Taihu Lake

Meiliang Bay and Gonghu Bay, in the north of Taihu Lake, are important water sources for the city of Wuxi, and increased eutrophication now threatens the safety of drinking water. The distribution of nitrogen (N) speciation and source of N in the surface waters in the north of Taihu Lake is studied, which was an important first step in controlling N pollution. The result shows that the average concentration of ammonia (NH₄ ⁺) and nitrate (NO₃ ^?) of surface water in Meiliang Bay was 0.32 and 0.35 mg/L, while 0.21 and 0.74 mg/L of Gonghu Bay, in which both bays had serious nitrate pollution. The concentrations of NH₄ ⁺ and NO₃ ^? in the surface water of the two bays had a trend of gradual decrease from north to south. The maximum concentrations of NH₄ ⁺ and NO₃ ^? of two bays were observed near the inflowing rivers, and the maximum concentrations of NH₄ ⁺ in surface water of two bays were 0.49 and 0.61, and 0.77 and 1.38 mg/L of NO₃ ^?. The concentration of NH₄ ⁺ in the interstitial water of the two bays had a trend of gradual decrease from west to east, but NO₃ ^? had the opposite tendency. The maximum concentrations of NH₄ ⁺ in the interstitial water of the two bays were 5.88 and 4.64, and 3.58 and 7.18 mg/L of NO₃ ^?. The exchangeable NH₄ ⁺ content in the sediment of Meiliang Bay had a trend of gradual decrease from north to south, but Gonghu Bay showed the reverse. The exchangeable NO₃ ^? content in the sediment of Meiliang Bay had a trend of gradual decrease from east to west, but a decreasing trend from north to south was observed in Gonghu Bay. The maximum concentrations of exchangeable NH₄ ⁺ were determined, and the values were 96.25 and 74.90 mg/kg, as well as NO₃ ^? with the values of 12.06 and 7.08 mg/kg. Chemical fertilizer and domestic sewage were the major sources of nitrate in surface water of Gonghu Bay, contributing 39.16 and 47.79%, respectively. Domestic sewage was the major source of nitrate in Meiliang Bay, contributing 84.79%. The denitrification process in Gonghu Bay was more apparent than in Meiliang Bay. Mixing and dilution processes had important effects on changing the concentration of nitrate transportation in the two bays.     

A case study considering the comparability of mass and volumetric suspended sediment data

Contemporary real-time instruments that advance suspended sediment monitoring capabilities often provide results in units (e.g. volumetric) that are not easily comparable to traditional mass (e.g. gravimetric) methods. A Midwest case study was initiated to assess the accuracy of three methods commonly used to convert volumetric data to mass. Water samples from rural, suburban, and urban stream reaches were analyzed for suspended sediment concentration using laser diffraction and wet sieving methods, resulting in paired volumetric (μl/l) and mass (mg/l) suspended sediment concentrations. Observed volumetric data were converted to mass using an assumed particle density (Pd) of 2.65 g/cm³, a calculated Pd, and linear regression. Using the assumed Pd, estimated mass data differed from observed mass data by as much as 60 %. Dividing mass concentration (mg/l) by the volumetric concentration (μl/l) resulted in site-specific average suspended sediment particle densities ranging from 2.17, 1.99, 1.76 g/cm³ for different land use types. Using a calculated Pd, estimated mass data differed from observed mass data by as much as 45 %. Paired sample t tests showed observed and estimated mass values to be significantly different (p < 0.01). R ² values for regression equations ranged from 0.82 to 0.88. Conversion difficulties likely result from temporal and spatial variations of Pd. The results illustrate the imprecision of conversion methods and highlight possible estimation errors assuming idealized conditions. Continued work is necessary to improve quantitative relationship(s) between mass and volumetric suspended sediment data and the utility of both types of information for science and land management practices.     

Major,minor element chemistry and oxygen and hydrogen isotopic compositions of Marun oil‐field brines,SW Iran: Source history and economic potential

Cation and anion concentrations and oxygen and hydrogen isotopic ratios of brines in the Asmari Formation (Oligocene–early Miocene) from the Marun oil field of southwest Iran were measured to identify the origin of these brines (e.g. salt dissolution vs. seawater evaporation) as well as the involvement of water–rock reaction processes in their evolution. Marun brines are characterized by having higher concentrations of calcium (11 000–20 000 mg/L), chlorine (120 000–160 000 mg/L) and bromide (600–1000 mg/L) compared to modern seawater. Samples are also enriched in ¹⁸O relative to seawater, fall to the right of the Global Meteoric Water Line and local rain water, and plot close to the halite brine trajectory on the δD versus δ¹⁸O diagram. Geochemical characteristics of Marun brines are inconsistent with a meteoric origin, but instead correspond to residual evaporated seawater modified by water–rock interaction, most significantly dolomitization. In addition, anhydrite precipitation or sulphate reduction appears to be important in chemical modification of the Marun brines, as indicated by lower sulphate contents relative to evaporated seawater. Extensive dolomitization, the presence of anhydrite nodules and high salinity fluid inclusions in the upper parts of the Asmari Formation fit a model whereby the Marun brines likely originated from the seepage reflux of concentrated seawater during the deposition of the overlying Gachsaran Formation evaporites in the Miocene. Copyright © 2010 John Wiley & Sons, Ltd.     

Salinity mapping model and brine chemistry of Mishrif reservoir in Basrah oilfields,Southern Iraq

Cation and anion concentrations and boron isotopic ratio of brines in the Mishrif Formation (U. Campanian-Tuoronian) from North Rumaila, South Rumaila, Majnoon, Zubair, and West Qurna oilfields southern Iraq were investigated. The aims of this study are to define the type, origin of the oilfield waters, and its flow model in the subsurface oil traps. Mishrif brines are characterized by having higher concentrations of sodium (50,500–84,200 ppm), chlorine (102,100–161,500 ppm), and boron (21.9–31.1 ppm) with lower sulfate contents (187–1350 ppm) relative to the modern seawater. Samples have slightly depleted in δ ¹¹B (35.4‰) relative to seawater fall near the seawater intrusion of the diagram Cl/Br Vs δ ¹¹B and occupied the field of evaporated seawater on the diagrams of Cl vs B and 1/Br vs δ ¹¹B. The brine of Na-chloride type is characteristics of the Mishrif reservoir in all oilfields except WQ which defined by facies of Na-Ca-chloride type. A weak acidic brine of a salinity six-time greater than seawater plays a role in generating the formation pressure and controlling the fluid flow. The reservoir rock-fluid interactions were interpreted using boron isotopes which eventually reveal an ongoing dilution process by the present seawater intrusion and injection water used for the secondary production under conditions of high-temperature digenetic reactions. The ¹¹B in the oilfield water is resulted from uptake of the tetrahedral borate after precipitation of calcium carbonate, while ¹⁰B is sourced from the thermal maturation of organic matters.     

Paleoenvironmental conditions and strontium isotope stratigraphy in the Paleogene Gafsa Basin (Tunisia) deduced from geochemical analyses of phosphatic fossils

Fossil shark teeth and coprolites from three major phosphorite occurrences in the Gafsa Basin (southwestern Tunisia) were investigated for their geochemical compositions to improve local stratigraphy and to better assess paleoenvironmental conditions. ⁸⁷Sr/⁸⁶Sr isotope ratios of shark teeth from the Early Maastrichtian El Haria Formation and from the Early Eocene Métlaoui s.s. Formation yielded Sr isotope ages of 68 ± 1 and 47.9 ± 1.3 Ma, respectively, which accord with the expected stratigraphic positions of these sediments. Conversely, shark teeth from the Paleocene–Eocene Chouabine Formation have large variation in Sr isotope ratios even within individual layers. After statistical treatment and then elimination of certain outlier samples, three age-models are proposed and discussed. The most reasonable solution includes three subsequent Sr ages of 61.8 ± 2.2 Ma, 57.2 ± 1.8 and 54.6 ± 1.6 for layer IX, layers VIII–V and layers IV–0, respectively. Three scenarios are discussed for explanation of the presence of the outliers: (1) diagenesis, (2) re-working and (3) locally controlled seawater Sr isotope ratio. The most plausible account for the higher ⁸⁷Sr/⁸⁶Sr ratios relative to the global ocean in some fossils is enhanced intrabasinal re-working due to low sea level. Conversely, the sample with lower ⁸⁷Sr/⁸⁶Sr than the global seawater may link to diagenesis or to seawater influenced by weathering of Late Cretaceous marine carbonates, which latter is supported by model calculation as well. The ε_Nd values of these fossils are very similar to those reported for Paleogene and Late Cretaceous Tethyan seawater and are compatible with the above interpretations. The relatively low oxygen isotope values in shark teeth from the topmost phosphate bed of the Chouabine Formation, together with the Sr isotope results, point toward recovering better connections with the open sea. These δ¹⁸O data reflect elevated ambient temperature, which may link to the Early Eocene Climatic Optimum.     

Radiation impact assessment of naturally occurring radionuclides and magnetic mineral studies of Bharathapuzha river sediments,South India

The natural radioactivity levels and magnetic measurements in sediment samples of Bharathapuzha river for the first time have been determined. Bottom sediments from 33 locations were collected to determine ²²⁶Ra, ²³²Th and ⁴⁰K using a HPGe detector based on the high-resolution gamma spectrometry system, and magnetic susceptibility by using Bartington MS2 magnetic susceptibility meter. The calculated activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K have been found to vary from 21.21 to 66.03 Bq kg^?1, 33.49 to 93.10 Bq kg^?1 and 232.25 to 899.66 Bq kg^?1, respectively. The results have been compared with worldwide recommended values and also with radioactivity measurements in river sediments of India and other parts of the world. The air-absorbed dose rate, indoor and outdoor annual effective dose rates and radium equivalent activity are calculated with an aim to access the radiation hazards arising due to the use of these materials in the construction of buildings and their mean values obtained are 74.83 nGy h^?1, 367.08 μSv y^?1, 91.77 μSv y^?1 and 157.09 Bq kg^?1, respectively. The mass-specific magnetic susceptibility values ranged widely from 35.4 to 2,160.5 × 10^?8 m³ kg^?1 and compared with other rivers in South India. Multivariate statistical analyses were performed to describe the magnetic and radioactivity relevance of the different groups of samples. The data obtained in the present study may be useful for radiological and magnetic mapping of the study area in the future.     

Factors influencing methane-derived authigenic carbonate formation at cold seep from southwestern Dongsha area in the northern South China Sea

This paper carried out mineral and geochemical studies on a profile through a diagenetic methane-derived authigenic carbonate sample that was collected from southwestern Dongsha area of the northern South China Sea. Five samples locating in the cross-sectional middle mainly consist of dolomite and quartz, and two samples close to the surface have a small amount of Mg-calcite. The δ¹³C values of the samples vary between ?30.59 and ?0.30 % VPDB, with δ¹⁸O values ranging from 3.07 to 3.59 % VPDB, δ^44/40Ca values ranging from 1.35 to 1.47 % SRM915a, indicating a contribution of methane to the carbon pool where the precipitation of authigenic carbonates occurred. Based on the isotope values alone, it can not be distinguished if the carbon source is thermogenic gas or a mixture of biogenic methane and marine dissolved inorganic carbon. The δ¹⁸O values are in general consistent with dolomite precipitation from a fluid similar to present seawater. The observed small variation might be related to the oxygen isotope composition of seep fluid. The relative small range in calcium isotope values suggests that relatively constant growth conditions and precipitation from seawater. The central part of the carbonate nodule formed under the strong influence of methane seepage, and the external part is less influenced by methane, either due to reduced methane flux to the surface or caused by erosional exhumation of the carbonate nodule from greater depth to the sediment surface.