Assessment of natural radioactivity in aquifer medium bearing uranium ores in Koprubasi,Turkey

Koprubasi, located within Manisa Province near the Izmir, is the biggest uranium mine where uranium ores originate from Neogene aged altered sandstone and conglomerate layers. The main objective of this study is to determine the radiation hazard associated with radioactivity levels of uranium ores, and the rocks and sediments around Koprubasi. In this regard, measured activity levels of ²²⁶Ra, ²³²Th and ⁴⁰K were compared with world averages. The average activity levels of ²²⁶ Ra, ²³²Th and ⁴⁰K were measured to be 5369.75, 124.78 and 10.0 Bq/kg in uranium ores, 24.32, 52.94 and 623.38 Bq/kg in gneiss, 46.24, 45.13 and 762.26 Bq/kg in sandstone and conglomerate, 73.11, 43.15 and 810.65 Bq/kg in sediments, respectively. All samples have high ²²⁶Ra and ⁴⁰K levels according to world average level. As these sediments are used as construction materials and in agricultural activities within the study area, the radiation hazard are calculated by using dose rate (D), annual effective dose rate (He), radium equivalent activity (Ra_eq) and radiation hazard index (I_yr). All the samples have Ra_eq levels that are lower than the world average limit of 370 Bq/kg. On the other hand, D, He and I_yr values are higher than world average values. These results indicate that the uranium ores in the Koprubasi is the most important contributor to the natural radiation level. The radioactivity levels of sediments and rocks make them unsuitable for use as agricultural soil and as construction materials. Moreover, it is determined that shallow groundwater in sediments and deep groundwater in conglomerate rocks and also surface water sources in the Koprubasi have high ²²⁶Ra content. According to environmental radioactive baseline, some environmental protection study must be taken in Koprubasi uranium site and the environment.     

Natural radioactivity in sediment of Wei River,China

The concentrations of natural radionuclides in sediment of Wei River of China were measured using γ-ray spectrometry with the aim of estimating the radiation hazard as establishing a database for radioactivity levels of river sediment of China. The activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K in sediment samples ranged from 10.4 to 39.9 Bq kg⁻¹, 15.3 to 54.8 Bq kg⁻¹ and 514.8 to 1,175.5 Bq kg⁻¹, respectively. The concentrations of these radionuclides were compared with the typical world values and the average activities of Chinese soil and Shaanxi soil. Radium equivalent activity (Ra_eq), external hazard index (H _ex) and representative level index (I _γr) were calculated for the samples to assess the radiation hazards arising due to the use of these sediment samples in the construction of dwellings. All the sediment samples have Ra_eq lower than the limit of 370 Bq kg⁻¹, H _ex less than unity and I _γr close to 1 Bq kg⁻¹. The overall mean outdoor terrestrial gamma dose rate is 64.8 nGy h⁻¹ and the corresponding outdoor annual effective dose is 0.079 mSv. None of the studied location is considered a radiological risk and sediment can be safely used in construction.     

Gamma radiation levels in the villages of South Konkan,Maharashtra, India

Ambient gamma radiation study was carried out in South Konkan using thermo luminescent dosimeters (TLDs). A statistical analysis was carried out to understand the distribution of gamma radiation in the study area. The annual effective doses (AEDs) received by the local population from the selected villages were 0.31 and 0.09 mSv year^?1 for indoor and outdoor locations, respectively. For indoor conditions, the maximum dose rate occurred for winter season and the minimum occurred in monsoon season while for outdoor conditions the maximum dose rate occurred in spring season and minimum occurred in the monsoon season. The terrestrial radioactivity in the corresponding villages was measured by a HpGe detector. The radiation hazard indices like absorbed dose rate in air (D), radium equivalent activity (Ra_eq), external hazard index (H _ex) and internal hazard index (H _in), and AED were calculated using soil radioactivity data. The minimum absorbed dose rate in air (33.97 nGy h^?1) corresponds to the Dale village and the maximum (101.86 nGy h^?1) corresponds to the Mithgawane village. Radiation hazard indices as Ra_eq, H _ex, and H _in were found to be within the limit. The average AED from natural radionuclides was found to be lower than the worldwide value. The AEDs of this study were compared with previous studies carried out worldwide. A positive correlation was observed for the absorbed dose rate in air and the activity concentration of U-238, Th-232, and K-40. A positive correlation between activity concentrations of U-238, Th-232, and K-40 was also observed. The comparison between the AEDs calculated using absorbed dose measured by TLDs and the values calculated from soil’s gamma spectrometry showed some variation in the villages of South Konkan.     

A study on the measurement and analysis of radioactivity concentration and the ambient dose rate in soil on the playgrounds of elementary schools in the Gwangju area

The aim of this study was to obtain nationwide basic data on the distribution of environmental radiation in normal times and to compare the characteristics and distribution in many areas. The data obtained can contribute to improve the radioactivity analysis technology, public health, and the environment in the future. Ten elementary schools in the Gwangju area were selected and soil samples were taken from the playgrounds of the selected schools for analysis. A high-purity Ge (HPGe) semiconductor detector, a multi-channel analyzer (MCA), and a FH40G dose rate detector were used to measure the radioactivity concentration of K-40 and Cs-137, and the ambient gamma dose rate. According to the measured radioactivity concentrations of ⁴⁰K and ¹³⁷Cs, the K-40 concentration (Bq/kg dry) was measured at 723.61 ± 162.72, which was higher than the minimum detection limit (MDL). The Cs-137 concentration (Bq/kg dry) measured was 0.203 ± 0.023, which was lower than the MDL. FH40G was used to measure the ambient gamma dose rate (nSv/h) in different areas. According to the measurement results, the ambient gamma dose rate was 176.73 ± 4.91. With regard to the correlation between the ambient gamma dose rate and radioactivity concentrations of ⁴⁰K and ¹³⁷Cs, ⁴⁰K showed a correlation coefficient with Cs-137 and the ambient gamma dose rate of ?0.36 and 0.124, respectively. ¹³⁷Cs revealed a correlation coefficient of 0.293 with an ambient gamma dose rate of ?0.210. In conclusion, the low correlation coefficient (<0.5) indicates no significant correlation between the ambient dose rate measurements of K-40 and ¹³⁷Cs.     

Elucidation of different forms of organic carbon in marine sediments from the Atlantic coast of Spain using thermal analysis coupled to isotope ratio and quadrupole mass spectrometry

Analysis of river, estuary and marine sediments from the Atlantic coast of Spain using thermogravimetry–differential scanning calorimetry–quadrupole mass spectrometry–isotope ratio mass spectrometry (TG–DSC–QMS–IRMS) was used to (a) distinguish bulk chemical hosts for C within a sediment and humic acid fraction, (b) track C pools with differing natural C isotope ratios and (c) observe variation with distance from the coast. This is the first application of such a novel method to the characterisation of organic matter from marine sediments and their corresponding humic acid fractions. Using thermal analysis, a labile, a recalcitrant and a refractory carbon pool can be distinguished. Extracted humic fractions are mainly of recalcitrant nature. The proportion of refractory carbon is greatest in marine sediments and humic acid fractions. Quadrupole mass spectrometry confirmed that the greatest proportion of m/z 44 (CO₂) and m/z 18 (H₂O) were detected at temperatures associated with recalcitrant carbon (510–540 °C). Isotope analysis detected progressive enrichment in δ¹³C for the sediment samples with an increase in marine influence. Isotopic heterogeneity in the refractory organic matter in marine sediments could be due to products of anthropogenic origin or natural combustion products. Isotope homogeneity of humic acids confirms the presence of terrigenous C in marine sediments, allowing the terrestrial input to be characterised.     

Gamma radiation measurements of naturally occurring radioactive samples from commercial Egyptian granites

Due to the widespread use of granites as building and ornamental materials, measurements of natural radioactivity for a total 27 selected samples of commercial granites used in Egypt were carried out by using a high pure germanium detector. The activity concentrations of ²²⁶Ra, ²³²Th and ⁴⁰K of commercial granites ranged from 25 to 356, 5 to 161, and 100 to 1,796?(Bq?kg^?1), respectively. The concentrations of these radionuclides are compared with the international recommended values. To evaluate the radiological hazard of the natural radioactivity, the radium equivalent activity, the absorbed dose rate, the effective dose rate, and the hazard index have been calculated. The radium equivalent activity Ra_eq varied from 41 to 669?(Bq?kg^?1) which exceeds the permitted value (370?Bq?kg^?1) and the internal hazard index H _in varied from 0.2 to 2.8 which is higher than 1. The absorbed dose rate due to the natural radioactivity in the samples under investigation ranged from 19 to 310?(nGy?h^?1). The total effective dose rates per person indoors were determined to be 0.09 to 1.5?(mSv?year^?1).     

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.     

Assessment of lifetime cancer risk from natural radioactivity levels in Kadikoy and Uskudar District of Istanbul

The activity concentrations of ²²⁶Ra, ²³²Th, and ⁴⁰K are measured in soil samples from various locations in the Kadikoy and Uskudar district of Istanbul (Turkey). The ²²⁶Ra activity concentrations range from 19.97 Bqkg^?1 to 50.80 Bqkg^?1 and average ²²⁶Ra concentration value 31.40 Bqkg^?1 was calculated. The ²³²Th activity concentrations range from 21.38 Bqkg^?1 to 52.61 Bqkg^?1 and average ²³²Th concentration value 34.44 Bqkg^?1 was calculated. The ⁴⁰K activity concentrations range from 464.06 Bqkg^?1 to 711.27 Bqkg^?1 and average ⁴⁰K concentration value 619.59 Bqkg^?1 was calculated. In addition, radium equivalent (Ra_eq), absorbed gamma dose rate (D), annual effective dose equivalent, (AEDE), excess lifetime cancer risk (ELCR) were calculated in this study. All of the calculations have been compared with both national and international standards and similar studies. As a result of this comparison, levels of natural radioactivity and radiological effects were slightly higher than the World average and Turkey.     

Denitrification pathways and rates in the sandy sediments of the Georgia continental shelf,USA

Denitrification in continental shelf sediments has been estimated to be a significant sink of oceanic fixed nitrogen (N). The significance and mechanisms of denitrification in organic-poor sands, which comprise 70% of continental shelf sediments, are not well known. Core incubations and isotope tracer techniques were employed to determine processes and rates of denitrification in the coarse-grained, sandy sediments of the Georgia continental shelf. In these sediments, heterotrophic denitrification was the dominant process for fixed N removal. Processes such as coupled nitrification-denitrification, anammox (anaerobic ammonium oxidation), and oxygen-limited autotrophic nitrification-denitrification were not evident over the 24 and 48 h time scale of the incubation experiments. Heterotrophic denitrification processes produce 22.8–34.1 μmole N m^-2 d^-1 of N₂ in these coarse-grained sediments. These denitrification rates are approximately two orders of magnitude lower than rates determined in fine-grained shelf sediments. These lower rates may help reconcile unbalanced marine N budgets which calculate global N losses exceeding N inputs.     

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.     

Radioelement Mapping and Environmental Monitoring of Surface Deposits using Ground Gamma Ray Spectrometry of the Area Adjacent to El‐Ramlah Village,Southwestern Sinai,Egypt

A ground‐based gamma‐ray survey has been performed in the area close to El‐Ramlah village, southwestern Sinai, Egypt, using a GS‐512 spectrometer. The main objective of this survey was to delineate radioactive anomalies within the surface of the study area and to identify the environmental effects of natural radioelements on the new inhabitants, Bedouins, who live in the recently built village in this region of the Sinai Peninsula. The results show that the maximum radioactivity of the total count component (T.C.) was about 15.7Ur at the northern part of the study area. The average radioelements concentration were 0.4% for potassium, 1.6 ppm for equivalent uranium and 4.5 ppm for equivalent thorium. To identify and map the environmental effects of the concentration of these radioelements on El‐Ramlah village, measurements of potassium (K%), equivalent uranium (eU) and equivalent thorium (eTh) were converted into an equivalent dose rate. The results illustrate that, the levels of effective dose rate of the natural radioactivity of the area of study remains in the safe range without any harm to living organisms, and it stays within the maximum permissible radiation dose rate (1.0 mSv y^?1) recommended by the International Commission of Radiological Protection.     

Benthic metabolism and nutrient cycling along an estuarine salinity gradient

Benthic metabolism and nutrient exchange across the sediment-water interface were examined over an annual cycle at four sites along a freshwater to marine transect in the Parker River-Plum Island Sound estuary in northeastern Massachusetts, U.S. Sediment organic carbon content was highest at the freshwater site (10.3%) and decreased along the salinity gradient to 0.2% in the sandy sediments at the marine end of the estuary. C:N ratios were highest in the mid estuary (23:1) and lowest near the sea (11:1). Chlorophyll a in the surface sediments was high along the entire length of the estuary (39–57 mg chlorophyll a m⁻²) but especially so in the sandy marine sediments (172 mg chlorophyll a m⁻²). Chlorophyll a to phaeophytin ratios suggested most chlorophyll is detrital, except at the sandy marine site. Porewater sulfide values varied seasonally and between sites, reflecting both changes in sulfate availability as overlying water salinity changed and sediment metabolism. Patterns of sediment redox potential followed those of sulfide. Porewater profiles of inorganic N and P reflected strong seasonal patterns in remineralization, accumulation, and release. Highest porewater NH₄ ⁺ values were found in upper and mid estuarine sediments, occasionally exceeding 1 mM N. Porewater nitrate was frequently absent, except in the sandy marine sediments where concentrations of 8 μM were often observed. Annual average respiration was lowest at the marine site (13 mmol O₂ m⁻² d⁻¹ and 21 mmol TCO₂ m⁻² d⁻¹) and highest in the mid estuary (130 mmol O₂ m⁻² d⁻¹ and 170 mmol TCO₂ m⁻² d⁻¹) where clam densities were also high. N₂O and CH₄ fluxes were low at all stations throughout the year: Over the course, of a year, sediments varied from being sources to sinks of dissolved organic C and N, with the overall spatial pattern related closely to sediment organic content. There was little correlation between PO₄ ³⁻ flux and metabolism, which we attribute to geochemical processes. At the two sites having the lowest salinities, PO₄ ³⁻ flux was directed into the sediments. On average, between 22% and 32% of total system metabolism was attributable to the benthos. The mid estuary site was an exception, as benthic metabolism accounted for 95% of the total, which is attributable to high densities of filter-feeding clams. Benthic remineralization supplied from less than 1% to over 190% of the N requirements and 0% to 21% of the P requirements of primary producers in this system. Estimates of denitrification calculated from stoichiometry of C and N fluxes ranged from 0% for the upper and mid estuary site to 35% for the freshwater site to 100% of sediment organic N remineralization at the marine site. We hypothesize that low values in the upper and mid estuary are attributable to enhanced NH₄ ⁺ fluxes during summer due to desorption of exchangeable ammonium from rising porewater salinity. NH₄ ⁺ desorption during summer may be a mechanism that maintains high rates of pelagic primary production at a time of low inorganic N inputs from the watershed.     

我国海洋地质分析测试技术

21世纪是海洋开发和利用的新世纪,随着国家对海洋地质调查工作的日益重视,海洋地质分析测试技术迎来了快速发展时期。本文对我国海洋地质分析测试技术的最新进展进行了简要评述:为满足海洋区域调查、海岸带地质调查的需要,建立了以大型分析仪器为主的多元素同时分析海洋地质样品的快速高效分析方法体系;针对新能源天然气水合物样品,开展了异常识别测试技术和应用测试技术研究,建立了用离子色谱法快速测定孔隙水中阴离子Cl^-、Br^-、SO₄^2-和阳离子Na⁺、NH₄⁺、K⁺、Ca²⁺、Mg²⁺ 的方法,开发出了以声学、电阻、时域反射(Time Domain Reflectometry, 简称为TDR)三种探测技术为主的适用于天然气水合物模拟实验的探测新技术;对于海洋沉积物中有机污染物样品,采用复合固相萃取净化柱,对海洋沉积物萃取液样品进行净化分离,依次选用正己烷和正己烷－二氯甲烷混合液淋洗固相萃取净化柱,可有效保留基体杂质,实现了海洋环境地质调查中基质复杂沉积物样品的同时净化、分离与测试,可显著提高实验效率;同时在大洋矿产样品分析技术、海洋地质标准物质研制、船载与原位化学探测技术等方面也取得了重要进展。本文还提出在海洋调查和监测的应用中,船载及原位测试技术将愈趋重要,加强海洋化学传感器的性能和检测集成化技术是今后的一个重要发展方向。     

Isotopic compositions of tropical East African flora and their potential as source indicators of organic matter in coastal marine sediments

The C and N stable isotope compositions of some flora of East Africa from coastal Tanzania and Amboseli National Park (Kenya) are used to assess if they can be used as a terrestrial end member during the estimation of terrestrial fraction in coastal marine sediments. The results of C isotope composition of various tree leaves, which average −29.3 ± 1.4%, indicate that these tropical higher land plant species follow a Calvin-Benson or non-Kranz (C₃) type of metabolism. The results for grass species, which average −13.2 ± 2.4%, indicate that most of them follow a Hatch-Slack or Kranz (C₄) type of metabolism. However, some of the succulent plants from the Amboseli National Park have δ¹³C values that average −14.7%, an indication that they follow a CAM (Crassulacean Acid Metabolism) type of metabolism. The N isotope values are relatively higher than expected for the terrestrial organic material. The average δ¹⁵N values for both tree and grass samples are higher than 5% and fall within the range normally considered to be marine. The high enrichment in ¹⁵N may be related to the environmental conditions in which plants thrive. Plants growing in sandy, dry and overgrazed environments are expected to be enriched in ¹⁵N owing to full utilisation of all available N species, regardless of their isotopic compositions. Other processes which may cause an enrichment in ¹⁵N include adsorption by various types of clay minerals, supply of ¹⁵N-enriched nitrate through sea-spray, and local denitrification, especially in swampy and lake margins where the input of organic matter may be higher than the rate of decomposition.The stable isotopic composition of organic C and N for surficial organic matter for the coastal marine sediments averages −17.0 ± 0.9% and 5.4 ± 1.1%, respectively. These values indicate a substantial contribution of C₄ plants and sea grasses. However, contribution of C₄ relative to that of sea grasses can not be evaluated owing to the fact that there is no significant difference in the isotopic compositions between the two groups.In the savannah environment, where a contribution from the C₄ types of plants might be substantial, the δ¹³C value for a terrestrial end member needs to be established prior to evaluation of the terrestrially derived organic matter in the marine environment. Owing to a significant contribution of sea grasses to the total organic matter preserved in coastal marine sediments, the stable isotopes of organic C seem to have a limited applicability as source indicators in the East African coastal waters. Furthermore, the results indicate that N stable isotopes seem to have a limited applicability as source indicators in coastal waters of East Africa. However, more work needs to be conducted to determine the terrestrial and sea grass end member values for the coastal areas.     

Evaluation of Naturally Occurring Radioactivity Materials (NORM) of Soil and Sediments in Oil and Gas Wells in Western Niger Delta Region of Nigeria

Oil mineral leases (30, 58 and 61) in Delta and River States are the major oil blocks in the oil and gas rich Niger Delta region of Nigeria that is characterized by environmental degradation from oil and gas activities. This research work presents an analytical approach on natural radioactivity assessment in soil and sediment in 15 oil fields of these OMLs. Concentrations of natural radionuclides (²²⁶Ra, ²³²Th and ⁴⁰K) were determined using gamma spectroscopy. The mean activity concentration of ²²⁶Ra, ²³²Th and ⁴⁰K for OML30 is 40.2 ± 5.1, 29.9 ± 4.2 and 361.5 ± 20.0 Bq kg^?1, respectively; the corresponding values obtained for OML58 is 20.9 ± 2.8, 19.4 ± 2.5 and 260.0 ± 14.1 Bq kg^?1, respectively. While the mean activity concentration of ²²⁶Ra, ²³²Th and ⁴⁰K for OML61 is 29.3 ± 3.5, 21.6 ± 2.6 and 262.1 ± 14.6 Bq kg^?1, respectively. These values obtained show enhanced NORMs, but are well within the world range and values reported in some regions and countries of the world, and are slightly above control values, values obtained in Southwestern region of Nigeria and some countries reported average values. The study also examined some radiation hazard indices, the mean values obtained are 86.6 ± 9.3 Bq kg^?1, 0.6 Bq kg^?1, 40.8 ηGy h^?1, 0.05 μSv y^?1, 0.2 and 0.3 for radium equivalent activity (Ra_eq), representative level index (Iγ), absorbed dose rates (D), annual effective dose rates (E _ff dose), external hazard index (H _ex) and internal hazard index (H _in), respectively. These calculated hazard indices to estimate the potential radiological health risk in soil and sediment are well below their permissible limits. The soil and sediments from the study area provide no excessive exposures for the inhabitants and can be used as construction materials without posing any radiological threat or harm to the public users. However, oil-field workers and host community residents are cautioned against excess exposure to avoid future accumulative dose of these radiations from sludge and sediment of this area.     

The supply and accumulation of silica in the marine environment

Rivers and submarine hydrothermal emanations supply 6.1 × 10¹⁴g SiO₂/yr to the marine environment. Approximately two-thirds of the silica supplied to the marine environment can be accounted for in continental margin and deep-sea deposits. Siliceous deep-sea sediments located beneath the Antarctic Polar Front (Convergence) account for over a fourth (1.6 × 10¹⁴g SiO₂/yr) of the silica supplied to the oceans. Deep-sea sediment accumulation rates beneath the Polar Front are highest in the South Atlantic with values as large as 53cm/kyr during the last 18.000 yr. Siliceous sediments in the Bering Sea, Sea of Okhotsk, and Subarctic North Pacific accumulate 0.6 × 10¹⁴g SiO₂/yr or 10% of the dissolved silica input to the oceans. The accumulation of biogenic silica in estuarine deposits removes a maximum of 0.8 × 10¹⁴g SiO₂/yr. Although estuarine silica versus salinity plots indicate extensive removal of riverine silica from surface waters, the removal rates must be considered as maximum values because of dissolution of siliceous material in estuarine sediments and bottom waters. Siliceous sediments from continental margin upwelling areas (e.g. Gulf of California, Walvis Bay, or Peru-Chile coast) have the highest biogenic silica accumulation rates in the marine environment (69 g SiO₂ cm²/kyr). Despite the rapid accumulation of biogenic silica, upwelling areas account for less than 5% of the silica supplied to the marine environment because they are confined laterally to such small areas.     

Dissolution of Carbonate Sediments Under Rising <Emphasis Type="Italic">p</Emphasis>CO<Subscript>2</Subscript> and Ocean Acidification: Observations from Devil’s Hole,Bermuda

Rising atmospheric pCO₂ and ocean acidification originating from human activities could result in increased dissolution of metastable carbonate minerals in shallow-water marine sediments. In the present study, in situ dissolution of carbonate sedimentary particles in Devil’s Hole, Bermuda, was observed during summer when thermally driven density stratification restricted mixing between the bottom water and the surface mixed layer and microbial decomposition of organic matter in the subthermocline layer produced pCO₂ levels similar to or higher than those levels anticipated by the end of the 21st century. Trends in both seawater chemistry and the composition of sediments in Devil’s Hole indicate that Mg-calcite minerals are subject to selective dissolution under conditions of elevated pCO₂. The derived rates of dissolution based on observed changes in excess alkalinity and estimates of vertical eddy diffusion ranged from 0.2 mmol to 0.8 mmol CaCO₃ m⁻² h⁻¹. On a yearly basis, this range corresponds to 175–701 g CaCO₃ m⁻² year⁻¹; the latter rate is close to 50% of the estimate of the current average global coral reef calcification rate of about 1,500 g CaCO₃ m⁻² year⁻¹. Considering a reduction in marine calcification of 40% by the year 2100, or 90% by 2300, as a result of surface ocean acidification, the combination of high rates of carbonate dissolution and reduced rates of calcification implies that coral reefs and other carbonate sediment environments within the 21st and following centuries could be subject to a net loss in carbonate material as a result of increasing pCO₂ arising from burning of fossil fuels.     

Natural and artificial radioactivity levels and hazards of soils in the Kücük Menderes Basin,Turkey

In this study, natural and artificial radionuclide activity concentrations in surface soils of Kücük Menderes Basin have been measured using gamma spectroscopy. The soil samples were collected from agricultural lands in the Kücük Menderes Basin in Turkey. The activity concentrations of ²²⁶Ra, ²³²Th, ⁴⁰K and ¹³⁷Cs in the soils were found to be range of 12.63 ± 2.28–72.51 ± 11.23, 11.45 ± 2.4–58.12 ± 4.76, 234.8 ± 14.85–1058.52 ± 24 Bq kg^?1 dw and 2.31 ± 0.18–7.75 ± 1.14 Bq kg^?1, respectively. The natural gamma radioactivity of the terrestrial radionuclides in soil samples and the gamma absorbed dose rate, the annual effective dose equivalent, the radium equivalent activity, the external hazard index, were calculated and compared with the international recommended values.     

Silicate weathering in anoxic marine sediments

Two sediment cores retrieved at the northern slope of Sakhalin Island, Sea of Okhotsk, were analyzed for biogenic opal, organic carbon, carbonate, sulfur, major element concentrations, mineral contents, and dissolved substances including nutrients, sulfate, methane, major cations, humic substances, and total alkalinity. Down-core trends in mineral abundance suggest that plagioclase feldspars and other reactive silicate phases (olivine, pyroxene, volcanic ash) are transformed into smectite in the methanogenic sediment sections. The element ratios Na/Al, Mg/Al, and Ca/Al in the solid phase decrease with sediment depth indicating a loss of mobile cations with depth and producing a significant down-core increase in the chemical index of alteration. Pore waters separated from the sediment cores are highly enriched in dissolved magnesium, total alkalinity, humic substances, and boron. The high contents of dissolved organic carbon in the deeper methanogenic sediment sections (50-150 mg dm⁻³) may promote the dissolution of silicate phases through complexation of Al³⁺ and other structure-building cations. A non-steady state transport-reaction model was developed and applied to evaluate the down-core trends observed in the solid and dissolved phases. Dissolved Mg and total alkalinity were used to track the in-situ rates of marine silicate weathering since thermodynamic equilibrium calculations showed that these tracers are not affected by ion exchange processes with sediment surfaces. The modeling showed that silicate weathering is limited to the deeper methanogenic sediment section whereas reverse weathering was the dominant process in the overlying surface sediments. Depth-integrated rates of marine silicate weathering in methanogenic sediments derived from the model (81.4-99.2 mmol CO₂ m⁻² year⁻¹) are lower than the marine weathering rates calculated from the solid phase data (198-245 mmol CO₂ m⁻² year⁻¹) suggesting a decrease in marine weathering over time. The production of CO₂ through reverse weathering in surface sediments (4.22-15.0 mmol CO₂ m⁻² year⁻¹) is about one order of magnitude smaller than the weathering-induced CO₂ consumption in the underlying sediments. The evaluation of pore water data from other continental margin sites shows that silicate weathering is a common process in methanogenic sediments. The global rate of CO₂ consumption through marine silicate weathering estimated here as 5-20 Tmol CO₂ year⁻¹ is as high as the global rate of continental silicate weathering.     

基于遗传算法的BP神经网络模型在岩心扫描仪测定海洋沉积物多种组分中的应用研究

海洋沉积物样品成分复杂,由于基体效应的影响,利用岩心扫描仪开展X射线荧光光谱分析只能得到目标元素的强度信息,不利于该方法在成矿机制和古环境等研究领域更好地发挥作用。本文采用岩心扫描仪测定海洋沉积物中的铝硅钾钙钛锰铁钒铬铜锌铷锶钇和铅15种元素,尝试引入BP神经网络模型利用其非线性拟合能力校正基体效应。实验表明,以水系沉积物、海洋沉积物和岩石国家标准物质以及定值海洋沉积物样品为训练样本,采用遗传算法优化BP神经网络的初始权值和偏置,可以有效校正除硅之外的14种元素基体效应的影响,实现了岩心扫描仪XRF测量结果由强度到浓度的转化。本方法的精密度为0.6%~6.8%(RSD,n=11),国家标准物质和海洋沉积物实际样品中15种组分的预测值与参考值的相对偏差在0.5%~17.5%之间,适合于海洋沉积物中多种主次量组分的快速分析,拓展了岩心扫描仪的功能。