The levels of fluorine in the sediments of the aquifer and their significance for fluorosis in coastal region of Laizhou Bay,China

The levels of fluorine in sediment cores obtained from Changyi County (PZ core) and Laizhou County (TS core) are used to discuss the fluorine sources in groundwater and its enrichment dynamics. The sediments in the aquifer are mainly constituted of granite gravels. The levels of fluorine in the PZ and TS cores range from 130 to 468 mg/kg, 139–528 mg/kg, with average values of 324, 348 mg/kg, respectively, which show relatively lower levels than the national average of fluorine in the soil or sediment. Thus, the fluorosis in this area should not be attributed to the levels of fluorine in sediments. The average fluorine concentrations in the aquifer from top to bottom are 154, 139, 200, 222 mg/kg for the TS core, and 154, 130, 266, 272 mg/kg for the PZ core, respectively, which are the lowest of the cores and extremely lower levels than the fresh granites. Such a fact indicates that a vast amount of fluorine has been leached into the groundwater. Moreover, the fluorine leachability is estimated to be approximately 70 %, although the previous documents showed fluorine contents of the granite surrounding Laizhou Bay were almost equal to or even lower than the average levels of fluorine in fresh granites. Meanwhile, a simulation experiment also reveals that fluorine release from rocks increases with the addition of seawater and brine water. Therefore, the seawater intrusion may potentially enhance the fluorine leachability, and should be an important dynamic of fluorine enrichment.     

Hydrogeochemical characterization and evolution of a regional karst aquifer in the Cuatrociénegas area,Mexico

The Cuatrociénegas area is useful for the investigation of the effect of groundwater extraction in the Chihuahuan freshwater xeric ecoregion. It has been investigated at this time using a selection of geochemical indicators (major, minor and trace elements) and δ³⁴S data, to characterize the origin of groundwater, the main geochemical processes and the mineral/groundwater interactions controlling the baseline geochemistry. The area is composed of limestones of Mesozoic age, with a composite thickness of about 500 m, overlaid by basin fill (poorly consolidated young sediments). Substantial water extraction and modification of natural discharges from the area along the last century have produced a detrimental impact on ecosystem structure and function. Water–rock interactions, mixing and evaporative processes dominate the baseline groundwater quality. Natural recharge is HCO₃–Ca type in equilibrium with calcite, low salinity (TDS?<?500 mg/L), Cl^? lower than 11 mg/L and average Li⁺ concentration of 0.005 mg/L. Along the groundwater flow systems, δ³⁴S evidence and mass transfer calculations indicate that Cretaceous gypsum dissolution and dedolomitization reactions adjust water composition to the SO₄–Ca type. The increase of water–rock interaction is reflected by Cl^? values increase (average 68 mg/L), TDS up to about 1500 mg/L and an average Li⁺ concentration of 0.063 mg/L. Calculations with chemical geothermometers indicate that temperature at depth could be at maximum of 15–20 °C higher than field-measured temperature for pozas. After groundwater is discharged to the surface, chemical evolution continues; water evaporation, CO₂ degassing and precipitation of minerals such as gypsum, calcite and kaolinite represent the final processes and reactions controlling water chemical composition.     

Vertical geochemical variations and arsenic mobilization in the shallow alluvial aquifers of the Chapai-Nawabganj District, northwestern Bangladesh: implication of siderite precipitation

Core sediments from three disturbed boreholes (JOR, GHAT, and RAJ) and two undisturbed boreholes (DW1 and DW2) were collected in the study area of the Chapai-Nawabganj district of northwestern Bangladesh for geochemical analyses. In the study area, groundwater samples from fourteen As-contained private wells and five nested piezometers at both the DW1 and DW2 boreholes were also collected and analyzed. The groundwater arsenic concentrations in the uppermost aquifer (10–40 m of depth) range from 3 to 315 μg/L (mean 47.73 ± 73.41 μg/L), while the arsenic content in sediments range from 2 to 14 mg/kg (mean 4.36 ± 3.34 mg/kg). An environmental scanning electron microscope (ESEM) with an energy dispersive X-ray spectrometer was used to investigate the presence of major and trace elements in the sediments. Groundwaters in the study area are generally the Ca–HCO₃ type with high concentrations of As, but low levels of Fe, Mn, NO₃ ^? and SO ₄ ^?2 . The concentrations of As, Fe, Mn decrease with depth in the groundwater, showing vertical geochemical variations in the study area. Statistical analysis clearly shows that As is closely associated with Fe and Mn in the sediments of the JOR core (r = 0.87, p < 0.05 for Fe and r = 0.78, p < 0.05 for Mn) and GHAT core (r = 0.95, p < 0.05 for Fe and r = 0.93, p < 0.05 for Mn), while As is not correlated with Fe and Mn in groundwater. The comparatively low Fe and Mn concentrations in some groundwater and the ESEM image revealed that siderite precipitated as a secondary mineral on the surface of the sediment particles. The correlations along with results of sequential extraction experiments indicated that reductive dissolution of FeOOH and MnOOH represents a mechanism for releasing arsenic into the groundwater.     

The landscape-scale relationship between lake sediment geochemistry and catchment bedrock composition from the Temagami and Gowganda areas of Northeastern Ontario,Canada

Lake sediments are integrators of watershed wide environmental information that includes bedrock geology, glacial overburden, vegetation, hydrology and land use. Lake sediments were collected from an area covering approximately 13,600 km² from the Gowganda and Temagami regions to determine the geochemical background conditions representing different bedrock types. For the entire dataset, the median value for arsenic in lake sediment was 2.6 mg/kg, well within the prescribed limits indicating that the Canadian national objective for arsenic in sediments for the protection of aquatic life (17 mg/kg). Overall, the vast majority of lake sediment samples (97.2%) were below the 17 mg/kg Canadian objective for the protection of aquatic life, however, catchments with Nipissing Diabase had the highest background levels for arsenic (10 mg/kg) with some lakes ranging up to 30 mg/kg. The major geological controls influencing changes in lake sediment geochemistry were determined using random forest classification and principal component analysis (PCA). Random forest classification was able to identify which geological province the samples were derived from and the dominant rock types in the sample catchment with respectable accuracy. PCA revealed strong spatial relationships between lake sediment geochemistry and bedrock geology, particularly a strong relationship between Nipissing Diabase in the watershed of the lake and the cobalt-type mineralization indicator elements in the lake sediment including naturally higher levels of arsenic. Within the samples that exceeded regulatory standards, over half the samples that exceeded the regulatory objectives were located in watersheds that contained Nipissing Diabase in their catchment. This study demonstrates that unique geochemical assemblages can be associated with specific geological areas which is of interest to exploration geologists, for target generation and prospecting, and to environmental policy makers, for site-specific restoration targets.     

Effect of agricultural land use on the chemistry of groundwater from basaltic aquifers, Jeju Island, South Korea

Geochemical processes were identified as controlling factors of groundwater chemistry, including chemical weathering, salinization from seawater and dry sea-salt deposition, nitrate contamination, and rainfall recharge. These geochemical processes were identified using principal component analysis of major element chemistry of groundwater from basaltic aquifers in Jeju Island, South Korea, a volcanic island with intense agricultural activities. The contribution of the geochemical processes to groundwater chemistry was quantified by a simple mass-balance approach. The geochemical effects due to seawater were considered based on Cl contributions, whereas the effects due to natural chemical weathering were based on alkalinity. Nitrogenous fertilizers, and especially the associated nitrification processes, appear to significantly affect groundwater chemistry. A strong correlation was observed between Na, Mg, Ca, SO₄ and Cl, and nitrate concentrations in groundwater. Correspondingly, the total major cations, Cl, and SO₄ in groundwater were assessed to estimate relative effect of N-fertilizer use on groundwater chemistry. Cl originates more from nitrate sources than from seawater, whereas SO₄ originates mostly from rainwater. N-fertilizer use has shown the greatest effect on groundwater chemistry, particularly when nitrate concentrations exceed 6–7 mg/L NO₃–N. Nitrate contamination significantly affects groundwater quality and 18% of groundwater samples have contamination-dominated chemistry.     

Environmental hazard analysis of a gypsum karst depression area with geophysical methods: a case study in Sivas (Turkey)

Because the mixture of seawater and freshwater in the Gyeongin-Ara Waterway in South Korea can lead to the intrusion of saline water into surrounding aquifers, systematic management through the establishment of a groundwater protection area is required. The analytic hierarchy process (AHP) model is used to delineate this protection area based on two primary factors and five secondary factors related to saline water intrusion. The study area is divided into 987 gridded cells with a unit size of 100 × 100 m, and the final evaluation score for each cell is calculated using the AHP model. Consequently, several artificial neural network models based on a multilayer perceptron are developed using the AHP’s secondary criteria and the evaluation score. Comparing the evaluation scores of ANN and AHP, more than 180 samples are required in the ANN model to insure high R2 between the original and estimated values. The ANN model is more consistent than the AHP model when determining groundwater protection area, because it can be re-constructed due to the changes in some secondary criteria and also changed due to a standardization process. The final evaluation score by the ANN model based on 300 samples, with the highest R2, is calculated and the regions with a score higher than 2.0 are selected as the groundwater protection area, accounting for 15% of the total cells. This area is similar to the range within approximately 200 m of the GA Waterway and also includes some changing sites in hydrogeochemistry and electric conductivity, which is produced by saline water intrusion. If the land-use type, groundwater levels, and some other criteria change at any cell, the ANN model can be re-executed to verify whether the cell belongs to a groundwater protection area. Considering that salinity of groundwater near the waterway can be affected by various factors including well depth, pumping conditions, and groundwater levels, the ANN model, which is a non-linear model, can be more effective for prediction than the AHP model.     

Soil microbial community response to seawater intrusion into coastal aquifer of Donghai Island,South China

Due to the sea level rise and the excessive exploitation of freshwater, seawater intrusion is becoming a critical issue. To clarify the degree of seawater intrusion in Donghai Island and the microbial community structure and functional response to seawater intrusion, groundwater samples and sediment samples were collected at profiles A, B; the profiles were along the direction of groundwater flow, perpendicular to the coastline, a hydrogeochemical survey and soil microbial community analysis were also performed. The hydrogeochemistry analysis showed that the chemical type of groundwater was Na–Cl, brackish water was dominant in the area, and coastal groundwater was strongly affected by seawater intrusion. The effect of seawater intrusion on structural and functional diversity of soil microbes was analyzed from soil samples of the study area, by polymerase chain reaction denaturing gradient gel electrophoresis (PCR-DGGE). The results of DGGE patterns and phylogenetic tree show that the extent of seawater intrusion has directly influenced soil microbial community structure. The changes of microbial community structure might be related to the major elements’ concentrations in groundwater. Phylogenetic affiliation indicated that γ-proteobacteria were dominated in the profile A, while β-proteobacteria were mainly appeared in the profile B. The Flavobacteriaceae was only appeared at the shrimp ponds nearby.     

Fingerprinting groundwater salinity sources in the Gulf Coast Aquifer System,USA

Understanding groundwater salinity sources in the Gulf Coast Aquifer System (GCAS) is a critical issue due to depletion of fresh groundwater and concerns for potential seawater intrusion. The study objective was to assess sources of groundwater salinity in the GCAS using ～1,400 chemical analyses and ～90 isotopic analyses along nine well transects in the Texas Gulf Coast, USA. Salinity increases from northeast (median total dissolved solids (TDS) 340 mg/L) to southwest (median TDS 1,160 mg/L), which inversely correlates with the precipitation distribution pattern (1,370– 600 mm/yr, respectively). Molar Cl/Br ratios (median 540–600), depleted δ²H and δ¹⁸O (?24.7‰, ?4.5‰) relative to seawater (Cl/Br ～655 and δ²H, δ¹⁸O 0‰, 0‰, respectively), and elevated ³⁶Cl/Cl ratios (～100), suggest precipitation enriched with marine aerosols as the dominant salinity source. Mass balance estimates suggest that marine aerosols could adequately explain salt loading over the large expanse of the GCAS. Evapotranspiration enrichment to the southwest is supported by elevated chloride concentrations in soil profiles and higher δ¹⁸O. Secondary salinity sources include dissolution of salt domes or upwelling brines from geopressured zones along growth faults, mainly near the coast in the northeast. The regional extent and large quantities of brackish water have the potential to support moderate-sized desalination plants in this location. These results have important implications for groundwater management, suggesting a current lack of regional seawater intrusion and a suitable source of relatively low TDS water for desalination.     

Assessment of organic pollutants (PAH and PCB) in surface water: sediments and shallow groundwater of Grombalia watershed in northeast of Tunisia

Toxic organic compounds in wastewater are serious threats for both human and environment healthy states. This study investigates the potential sources of surface water, sediment and groundwater pollution by polycyclic aromatic hydrocarbons (PAHs) and polychlorinated biphenyl (PCBs) as discharged by wastewater into the River of Oued El bey in northeastern Tunisia. Analysis indicates that the concentration of PAHs and PCBs are high in wastewater and vary from 0.37 to 0.83 mg/L and from 0.28 and 1.18 mg/L, respectively. The spatial distribution of PAHs and PCB in surface water showed a variation between 0.37 to 9.91 mg/L and between 0.1 to 0.47 mg/L, respectively. However, the quality of surface water is changed after wastewater evacuation at Oued Tahouna. The determination of PAH and PCB pollutants in groundwater shows a great interest in the development of water resources. The Concentration of these pollutants varying from 0.0204 to 1.93 mg/L and from 0.0052 to 0.196 mg/L, respectively. For PAH, analysis reveals also that naphtelene, fluorene, anthracene and chrysene are the most detected PAHs compounds in water and sediment samples while benzo[b]fluoranthene and benzo[a]pyrene are less present and in trace level. Higher concentrations of PAHs and PCBs are found in samples taken close to industrial areas of Bouargoub and Soliman, and wastewater discharge locations in Soliman. Analysis of the spatial distribution of PAHs and PCBs clearly link their higher concentration in water and sediments to wastewater and manufacturing discharges in the study area. In surface sediment, the organic pollutants are present. The cluster analysis for organic pollutants in different state and different matrix highlight a relationship between the wastewater evacuation and the water qualities which confirmed the direct response of the pollution sources on the surface water and groundwater organic pollution quality.     

Determining groundwater protection zones for the Quaternary aquifer of northeastern Nile Delta using GIS-based vulnerability mapping

The area of study lies at the northeastern part of Nile Delta. Global shoreline regression and sea-level rise have their own-bearing on the groundwater salinization due to seawater intrusion. A new adopted approach for vulnerability mapping using the hydrochemical investigations, geographic information system and a weighted multi-criteria decision support system (WMCDSS) was developed to determine the trend of groundwater contamination by seawater intrusion. Six thematic layers were digitally integrated and assigned different weights and rates. These have been created to comprise the most decisive criteria used for the delineation of groundwater degradation due to seawater intrusion. These criteria are represented by the total dissolved solids, well discharge, sodium adsorption ratio, hydrochemical parameter (Cl/HCO₃), hydraulic conductivity and water types. The WMCDSS modeling was tried, where a groundwater vulnerability map with four classes ranging from very low to high vulnerability was gained. The map pinpointed the promising localities for groundwater protection, which are almost represented by the very low or low vulnerability areas (53.69 % of the total study area). The regions having high and moderate groundwater vulnerability occupy 46.31 % of total study area, which designate to a deteriorated territory of groundwater quality, and needs special treatment and cropping pattern before use. However, the moderate groundwater vulnerability class occupies an area of about 28.77 % of the total mapped area, which highlighted the need for certain management practices to prevent the saltwater intrusion from expanding further to the south. There was a good correlation of the constructed vulnerability map with the recently gathered water quality data and hydrochemical facies evolution. The plotting of water quality data on Piper trilinear diagram revealed the evolution of freshwater into the mixing and the saline zones as an impact of seawater intrusion, which validates the model results.     

Spatial geochemical variation of major and trace elements in the marine sediments of Mumbai Harbor Bay

The resulting concentration data sets of major (Na, K, Mg, Ca and Fe) and trace elements (Cu, Ni, Co and Mn) in bed and suspended sediments were used to evaluate the enrichment factor for anthropogenic influences and principal component analysis for identifying the origin of source contributions in the studied area. Normalization of metals to Fe indicated that high enrichment factors in the bed sediment were in the order of Co > Cu > Na > Ca > Ni except Mg, K and Mn while for suspended sediments, only Co has a high enrichment factor. High enrichment of Co and Cu reflected the contamination of sediments from anthropogenic sources. The high influence of Na and Ca in sediments may be caused for seawater salinization factor. A significant positive correlation among enrichment factors of various elements of interest suggests a common origin/identical behavior during transport in the sediment system.     

Investigation of seawater intrusion in the Dibdibba Aquifer using 2D resistivity imaging in the area between Al-Zubair and Umm Qasr,southern Iraq

Electrical resistivity surveying for delineating seawater intrusion was performed in the Dibdibba aquifer in the area between the cities of Al-Zubair–Safwan and Al-Zubair–Umm Qasr in the vicinity of Khor AL-Zubair Channel, Basrah governorate, southern Iraq. Fourteen 2D resistivity profiles with a total length of 14 km were collected in the study area. The resistivity sections were compared with lithological data extracted from 11 boreholes. Thirty-nine groundwater samples were collected within the area and analyzed for chemical constituents; internal hydrogeological reports and unpublished studies were also evaluated. Results reveal the existence of three major resistivity layers, ranging from 0.1 to 130 Ωm at various depths and locations. The first layer has very low electrical resistivity (0.1–5 Ωm) representing a layer saturated with saltwater intruded from Khor AL-Zubair Channel. The second layer shows resistivity in the range of 5–130 Ωm, attributed to a transition zone and an unaffected zone saturated with brackish groundwater. The last resistivity layer (<?3 Ωm) represents coarse-grain sediments saturated with saline groundwater. Furthermore, a hard clay bed (Jojab) appears with a resistivity of 3–7 Ωm in all 2D imaging lines within a depth of 20–28 m. Electrical conductivity (EC) measurements from seven wells collected in 2014 and 2016 show a positive EC difference increasing landward with an average increase of 1927 µS/cm. In addition, six chemical relationships (Na/Cl, [Ca?+?Mg]/[HCO₃?+?SO₄], SO₄/HCO₃, SO₄/Cl, Mg/Ca and Cl/[HCO₃?+?CO₃]) are used to detect the source of salinity in groundwater. This study proves that extensive use of high-resolution 2D imaging sections, alongside lithological and hydrogeological data, can serve as a useful tool to delineate the boundaries between aquifers, identify hydraulic boundaries between groundwater with different salinities and allocate hard clay layers between the upper and lower Dibdibba aquifer. In general, the combination of 2D imaging and hydrochemistry enables conceptualization of the hydrogeological situation in the subsurface and characterization of the salinity source, here seawater intrusion, in the study area. There have been no studies published so far on the characteristics of saltwater intrusion in the study area, and this study is considered to be important for monitoring and studying the intrusion and regression of seawater.     

Salinity mapping of coastal groundwater aquifers using hydrogeochemical and geophysical methods: a case study from north Kelantan,Malaysia

Integrated hydrogeochemical and geophysical methods were used to study the salinity of groundwater aquifers along the coastal area of north Kelantan. For the hydrogeochemical investigation, analysis of major ion contents of the groundwater was conducted, and other chemical parameters such as pH and total dissolved solids were also determined. For the geophysical study, both geoelectrical resistivity soundings and reflection seismic surveys were conducted to determine the characteristics of the subsurface and groundwater contained within the aquifers. The pH values range from 6.2 to 6.8, indicating that the groundwater in the study area is slightly acidic. Low content of chloride suggests that the groundwater in the first aquifer is fresh, with an average concentration of about 15.8 mg/l and high geoelectrical resistivity (>45 ohm m). On the other hand, the groundwater in the second aquifer is brackish, with chloride concentration ranging from 500 mg/l to 3,600 mg/l and very low geoelectrical resistivity (<45 ohm m) as well as high concentration of total dissolved solids (>1,000 mg/l). The groundwater in the third aquifer is fresh, with chloride concentrations generally ranging from 2 mg/l to 210 mg/l and geoelectrical resistivity of greater than 45 ohm m. Fresh and saltwater interface in the first aquifer is generally located directly in the area of the coast, but, for the second aquifer, both hydrogeochemical and geoelectrical resistivity results indicate that the fresh water and saltwater interface is located as far as 6 km from the beach. The considerable chloride ion content initially suggests that the salinity of the groundwater in the second aquifer is probably caused by the intrusion of seawater. However, continuous monitoring of the chloride content of the second aquifer indicated no significant changes with time, from which it can be inferred that the salinity of the groundwater is not affected by seasonal seawater intrusion. Schoeller diagrams illustrate that sulphate concentrations of the groundwater of the second aquifer are relatively low compared to those of the recent seawater. Therefore, this result suggests that the brackish water in the second aquifer is probably from ancient seawater that was trapped within the sediments for a long period of time, rather than due to direct seawater intrusion.     

Heavy metal contamination in sediments of Balanagar industrial area,Hyderabad, Andra Pradesh,India

Environmental geochemical studies were carried out to find out the extent of contamination in sediments due to heavy metals in Balanagar industrial area, Hyderabad, Andhra Pradesh, India. The industrial area consisting of 350 small and large industries manufacturing battery, steel planting, pharmaceutical chemicals, metal plating, etc. The present study was undertaken on sediment contamination in Balanagar industrial area, to determine extent and distribution of heavy metals (Cu, Cr, Ni, Pb, Zn, As) and to delineate the source. There is no treatment plant in the industrial area, and many industries release the effluents into nearby nalas and lakes. Solid waste from the industries is also being dumped along the roads and near the open grounds due to which heavy metals migrate from solid waste to the groundwater. The sediments samples were collected from the study area in clean polythene covers and were analyzed for their heavy metals by X-ray fluorescence spectrometry. The concentration ranges of different heavy metals were Cr, 96.2–439.6 mg/kg; Cu, 95.7–810 mg/kg; Ni, 32.3–13,068.2 mg/kg; Pb, 59.2–512 mg/kg; Zn, 157.1–4,630.5 mg/kg; Co, 1.8–48.3 mg/kg; and V, 35.2–308.5 mg/kg. High concentration of heavy metals in sediments can be attributed to some pharmaceutical and metal industries in the study area. Based on the results obtained, suitable remedial measures can be adopted such as phytoremediation and bio-remediation for reduction of heavy metals in sediments.     

Phosphorus fractions and bioavailability in relation to particle size characteristics in sediments from Lake Hongfeng, Southwest China

Information on the chemical composition of phosphorus (P) fractions in sediments is fundamental to understanding P bioavailability and eutrophication in lake ecosystems. Phosphorus fractions and its bioavailability in sediments cores of Lake Hongfeng, southwest China, were investigated using a chemical sequential extraction scheme. Relationships between P fractions, P bioavailability and particle sizes were discussed. P fractions concentrations were ranked in the order: Residual-P > NaOH–rP > NaOH–NRP > HCl–P > BD–P > NH₄Cl–P, and all of them decreased with increasing sediment depth. Statistical analysis showed that concentrations of bioavailable P (BAP) which includes the NH₄Cl–P, BD–P, NaOH–rP and NaOH–NRP fractions ranged from 404.68 to 1,591.99 mg/kg and accounted for 26.8–71.8 % of the concentrations of total phosphorus (TP) in the top 5 cm sediments, whereas in the whole sediment cores, their concentrations ranged from 239.70 to 1,591.99 mg/kg and accounted for 26.8–76.0 % of TP. The results suggested that the sediments were a large potential source of P for algae blooms in Lake Hongfeng. Phosphorus fractions and their potential bioavailability were influenced by the sediment particle sizes, especially the bioavailability of the NH₄Cl–P fraction, which was strongly affected by the presence of fine particle sizes in the sediments.     

Use of hydrochemical parameters for the identification of fresh groundwater resources,Potharlanka Island,India

A hydrochemical study has been carried out on the fresh groundwater resources of Potharlanka, Krishna Delta, India. Groundwater samples were collected at 58 sites and analyzed in June and December 2001. The groundwater is mildly alkaline with a pH of 7.2–8.2, electrical conductivity (EC) varies from 645–4,700 µS/cm in June 2001 (pre-monsoon) and from 605–5,770 µS/cm in December 2001 (post-monsoon). More than 75% of the samples have >1000 mg/l TDS which is higher than the maximum permissible limit for potable water. Na and Cl are the dominating cations and these are directly proportional to TDS. Extremely low HCO ₃/Cl and variable high Mg/Ca (molar ratios) indicated the transformation of the fresh groundwater aquifer systems to saline. Groundwater of this island is classified as Na–Cl, Na–Ca–Cl–HCO ₃, Na–Mg–Cl–SO ₄ and mixed types. A high percentage of mixed water types indicates the possibility of simultaneous fresh groundwater dilution activity along with a seawater ingression/intrusion process. Low rainfall and excessive withdrawal of groundwater has caused the increase of saline water intrusion.     

Geochemistry of deep-sea sediments in two cores retrieved at the mouth of the Coatzacoalcos River delta,western Gulf of Mexico,Mexico

Coastal margins, especially the river-influenced coastal areas, are considered as active interfaces between the continental and oceanic environments, which have huge dispersal of detrital materials and heavy metal input. It is well determined that the fine-grained sediments are important reservoir for the accumulation of heavy metals. In this study, we analyzed the radiocarbon age, texture, organic matter, carbonate content, and geochemical compositions of two sediment cores (GM42 and GM44) retrieved in front of the Coatzacoalcos River mouth basin, southwestern Gulf of Mexico (～864 and 845 m water depth, respectively). Our objective was to infer the sedimentation rate, intensity of weathering, provenance, and influence of anthropogenic activities on heavy metal contamination in sediments. The radiocarbon-age measurements of mixed planktonic foraminifera for core GM44 reveals an age of 21,289 ± 136 cal. years B.P., which fall within the Late Glacial Maximum (LGM; 21000 ± 2000 years B.P). The calculated sedimentation rate for core GM42 (~0.013 cm/year) is lower than in core GM44 (0.022 cm/year), which is probably due to the variations in detrital sediment input and/or seafloor topography. The weathering indices such as chemical index of alteration (CIA), chemical index of weathering (CIW), and plagioclase index of alteration (PIA) suggested that the source area experienced low to moderate intensity of chemical weathering under warm to humid climatic conditions. The SiO₂/Al₂O₃, Al₂O₃/Na₂O, and K₂O/Al₂O₃ ratio values indicated moderate to high compositional maturity. The major and trace element concentrations suggested that the sediments were likely derived from intermediate source rocks. The heavy metal contents indicated that the sediments were not contaminated by the industrial waste disposals supplied by the Coatzacoalcos River. The redox proxy sensitive elements such as V, Cr, Cu, and Zn indicated an oxic depositional environment for the deep-sea sediment cores. The application of discrimination diagrams for the geochemistry data revealed a passive margin setting for the sediment cores. The compositional variations observed at the upper sections (<30 cm) between the two sediment cores revealed that the type of detrital sediments supplied by the Coatzacoalcos River to the deep sea area is not uniform, which is also revealed by the variation in sedimentation rate.     

Geochemical evolution and timescale of seawater intrusion into the coastal aquifer of Israel

This study is an attempt to quantify the geochemical processes and the timescale of seawater intrusion into a coastal aquifer from changes in the major ionic composition of the water and the natural distribution of the cosmogenic isotopes ¹⁴C and ³H. For that purpose, we sampled saline and brackish groundwaters from the Israeli coastal aquifer. A multilayer sampler (MLS) was used to obtain very high resolution (10 cm) profiles across the fresh-saline water interface (FSI).The chemical and stable isotope data revealed three distinct water types (end members) that are located in different zones on the route to the coastal aquifer: (1) slightly modified Mediterranean seawater (SWS); (2) slightly diluted (with up to 20% fresh groundwater) saline groundwater (SDS); and (3) fresh groundwater (FGW).The SWS samples generally show an excess of total alkalinity and total dissolved inorganic carbon (DIC), and a depletion of ¹³C_DIC and ¹⁴C_DIC with respect to normal seawater indicating that anaerobic oxidation of organic matter is the first diagenetic reaction that affects seawater during its penetration into the bottom sediments. SDS waters appear when SWS is slightly diluted, gain Ca²⁺ and Sr²⁺, and is depleted in K⁺, suggesting that the main processes that transform SWS into SDS are slight dilution with fresh groundwater and cation exchange. At the fresh-saline water interface, SDS generally shows conservative mixing with FGW.Inspection of chemical data from coastal aquifers around the world indicates that intensive ion exchange in slightly diluted saline groundwater is a globally important phenomenon of seawater intrusion. Most of our saline groundwater samples contain substantial amounts of ³H suggesting that penetration of Mediterranean seawater and its inland travel to a distance of 50-100 m onshore occurred 15-30 yr ago. This is supported by the ¹⁴C_DIC mass balance that explains the relatively low ¹⁴C_DIC activities in the SDS as influenced by diagenesis and not by simple radioactive decay.     

Spatial variations and distributions of phosphorus and nitrogen in bottom sediments from a typical north-temperate lake,China

Concentrations and vertical distributions of total nitrogen (TN), total phosphorus (TP) and their different forms in sediments obtained from nine locations of Lake Dalinouer in September 2008 were analyzed. The results demonstrated that TP in surface sediments ranged from 0.493 to 0.904 g/kg, and inorganic phosphorus was the main fraction of total phosphorus, ranging from 335 to 738 mg/kg. Simultaneously, the autogenetic calcium phosphorus (ACa-P) was the main fraction of inorganic phosphorus, ranging from 145.4 to 543.2 mg/kg. Vertical distribution of different phosphorus forms in different sediment cores was distinguishing, and most of them tended to increase toward the surface sediment, indicated that the phosphorus concentration was related to the humanity with a certain extent. The relationships between TP and occluded phosphorus and ACa-P were significant. Nitrogen in the sediment was composed mainly of organic nitrogen, accounting for grater than 80 % of TN. NO₃ ^?-N was the dominate fraction of inorganic nitrogen in the surface sediment, ranging between 51 and 346 mg/kg (151.1 ± 104.4 mg/kg), and accounting for between 2.2 and 17.7 % of total sediment nitrogen (6.2 ± 5.6 %). The ratio of organic carbon and TN in sediment was in range of 6.0–25.8 and presented a tendency of lake centre >lake sides, indicating that nitrogen accumulated in the sediments from lake sides came mainly from terrestrial source and nitrogen was mainly autogenetic in lake centre. Ratio of N:P in all sampling sites was below 14, indicated that N was the limiting nutrient for algal growth in this lake.