137Cs Inventory in Abiotic Component and Biota From the Aegean and Ionian Sea - Greece

This study deals with ¹³⁷Cs dispersion and behaviour in the Aegean and Ionian Sea based on work done during the period 1984-1994, as a brief general review. Sea water, sediment and marine biota were analysed and measured by gamma spectrometry and the activity concentrations of ¹³⁷Cs were evaluated with consideration to the sources of pollution. According to ¹³⁷Cs levels the period is distinguished into three sub-periods, the pre-Chernobyl, the early Chernobyl influence and the late Chernobyl influence period. During the early period of the Chernobyl accident the ¹³⁷Cs levels in the Greek marine environment increased roughly up to an order of magnitude if compared with the pre-accident ones. Since 1988, the late impact of the accident is focused mainly in the North Aegean Sea, at the Dardanelles mouth, due to the Black Sea outflow.     

Retention of 137cesium in acid sulphate soils of South Central Thailand

Adsorption and desorption of ¹³⁷Cs by acid sulphate soils from the Nakhon Nayok province, South Central Plain of Thailand located near the Ongkarak Nuclear Research Center (ONRC) were investigated using a batch equilibration technique. The influence of added limestone (12 and 18 tons ha^-1) on ¹³⁷Cs adsorption-desorption was studied. Based on Freundlich isotherms, both adsorption and desorption of ¹³⁷Cs were nonlinear. A large portion (98.26-99.97%) of added ¹³⁷Cs (3.7 × 10³-7.03 × 10⁵ Bq l^-1) was sorbed by the soils with or without added lime. The higher lime treatments, however, favoured stronger adsorption of ¹³⁷Cs as compared with soil with no lime, which was supported by higher K_ads values. The addition of lime, the cation exchange capacity and pH of the soil increased and hence favoured the stronger adsorption of ¹³⁷Cs. Acid sulphate soils with a high clay content, medium to high organic matter, high CEC, and predominant clay types consisting of a mixture of illite, kaolinite, and montmorillonite were the main soil factors contributing to the high ¹³⁷Cs adsorption capacity. Competing cations such as NH₄⁺, K⁺, Na⁺, Ca²⁺, and Mg²⁺ had little influence on ¹³⁷Cs adsorption as compared with liming, where a significant positive correlation between K_ads and soil pH was observed. The ¹³⁷Cs adsorption-desorption characteristics of the acid sulphate soils studied exhibited a very strong irreversible sorption pattern. Only a small portion (0.09-0.58%) of ¹³⁷Cs adsorbed at the highest added initial ¹³⁷Cs concentration was desorbed by four successive soil extractions. Results clearly demonstrated that Nakhon Nayok province acid sulphate soils have a high ¹³⁷Cs adsorption capacity, which limits the ¹³⁷Cs bioavailability.     

Radioactivity in the Baltic Sea

The Baltic Sea is, like the Mediterranean, a marginal sea, which with the Black Sea, were marine environments contaminated from the Chernobyl accident.

Radiocaesium and plutonium isotopes were studied in water, sediment and macroalgae in the Baltic Sea since 1982. the inventory of ¹³⁷Cs in the Baltic increased from 0.65 PBq to 5.85 PBq following the Chernobyl accident. the corresponding increase for ^{239 + 240}Pu was less significant and yielded 1.5 TBq to a total value of 16.5 TBq.

For plutonium, 98% is trapped in the sediment and the net-exchange of this element through the Baltic straits is very small (1 GBq/year), while for radiocaesium, 45% is in the water phase and there is a net-loss of 60 000 GBq annually into the adjacent water (Kattegatt).     

Radioactivity Monitored From Moored Oceanographic Buoys

The principles and operation of a gamma radiation sensor mounted on oceanographic buoys are described. the sensor has proved rugged in severe weather conditions and has satisfactory detection limits and accuracy. Continuous monitoring of artificially produced γ-emitters such as ¹³⁷Cs, ¹³⁴Cs, ¹³¹I, ¹³³I, ¹³²Te, naturally occuring emitters such as ⁴⁰k and ²¹⁴Bi in open sea conditions can provide important information in critical situations.     

The Existence and Removal of Evaporable 137Cs-Containing Compound(S) From the Extract of Lichen Cetraria Islandica

The aim of the work described here was to investigate the existence of evaporable ¹³⁷Cscontaining compound(s) in lichen and to suggest a possible way of dealing with a phenomenon during lichen exploitation. A sample of lichen, Cetraria islandica, was submitted to aqueous extraction and the extract was monitored to be ¹³⁷Cs-radioactive. It was heated according to the experimental schedule and the resulting vapour passed over a layer of activated charcoal. By measuring the decrease in the radioactivity content of the lichen extract after heating and the radioactivity of the adsorbent it was found that a significant amount of the extracted ¹³⁷Cs could be evaporated and bound to the charcoal adsorbent (40.6%). If not captured, this radiocaesium may lead to air pollution, especially of immediate breathing space.     

Distribution and Migration of some Metals in the Water-Sediment System Using Radiotracers

The knowledge of heavy metals and related radionuclide distribution, and accumulation among the different components of a fresh water ecosystem, plays a relevant role in environmental studies. In the present study reported here the behaviour of ⁶⁰Co, ¹³⁴Cs and ⁵⁴Mn was investigated in a water-sediment system. Water and sediment samples were obtained from an artificial channel, derived from the Po river near Serafini Island (middle course). It was characterized by a very low water flow.     

Inventories and Distribution of Radiocaesium in Arctic Marine Sediments: Influence of Biological and Physical Processes

Extensive surveys of sediment burdens of radiocaesium, specifically ¹³⁷Cs, and other radioactive contaminants in the Arctic during the 1990's, indicate that almost all anthropogenic radionuclides buried on continental shelves adjacent to Alaska are derived from global bomb fallout. the ¹³⁷Cs (half-life: 30.2y) activities observed in surface (0-4 cm) marine sediments however, vary widely, albeit much less than the expected current inventory resulting from bomb fallout at this latitude (∼100mBq cm^-2). This observed geographical variation provided the opportunity to evaluate physical and biological mechanisms that may affect caesium biogeochemistry on Arctic continental shelves. We investigated whether high biological productivity in portions of the Bering and Chukchi Seas is effective in removing dissolved radiocaesium from the water column, and whether biological production in overlying water affects total radiocaesium inventories in sediments. Based upon C/N ratios in the organic fraction of shallow sediments, we found no evidence that higher inventories or surface activities of radiocaesium are present in areas with higher deposition of particulate organic matter. Based upon stable carbon isotope ratios of organic matter in sediments, we found no evidence that terrestrial runoff contributes proportionally to higher surface activities, although terrestrial runoff may affect total inventories of the radionuclide. Radiocaesium content of surface sediments was significantly correlated with total organic carbon content of sediments and the proportion of sediments in the finest sediment fractions. Because high current flow can also be expected to influence distributions of those sedimentary parameters, we conclude that re-distribution of     

Radioactive Isotopes of Strontium, Caesium and Plutonium in Sediments of the Northern Adriatic Sea

Sediment samples of different strata (0-3 and 12-15 cm) were collected between 1990 and 1992 during seasonal cruises in the Northern Adriatic Sea. A complete mapping of the Sr-90, Cs-137, Pu-238 and Pu-239(240) concentrations was obtained for samples covering a wide area, stretching from the Gulf of Trieste towards the Ancona shoreline. Sr-90 concentrations varied between 1.5 and 6.5 Bq kg^-1 dw, Cs-137 was in the range 0.9-38.9 Bq kg^-1 dw, Pu-239(240) in the range 0.08-1.5 Bq kg^-1 dw and Pu-238 around 0.03 Bq kg^-1 dw. Special reference was also put on the comparison between the off-shore environment and data obtained from samples collected inside the Po river delta. in spite of the major accumulation of Cs-137 inside the estuarine environment, higher concentrations of strontium and plutonium isotopes were detected in the offshore environment.     

Accumulation and metal fluxes in the central Venice Lagoon during the last century

Samples from 18 short sediment cores were analyzed for major and trace metals (Al, Fe, Ca, K, Mg, Mn, Si, Ti, Pb, Zn, Cu, Ni, and Cr), ²¹⁰Pb, ¹³⁷Cs, total organic carbon, grain size, and mineralogical composition to find the record of major environmental changes, either natural or anthropogenic, and to establish their chronologies. Some sediments are characterized by nearly constant composition over time, but others clearly show signs of an increasing marine influence, as an increase of the carbonate contents, after the opening of the Malamocco-Marghera Canal in 1969. These changes sometimes obscure the real pattern of pollutants and tracers, which is revealed by normalization against Al. Zn is the most important contaminant, with concentration factors up to 9.3 times the background level, and the most contaminated sediments are those within a few kilometers from the industrial district of Porto Marghera. ²¹⁰Pb activity-depth profiles were used to calculate apparent accumulation rates that provide a basis for the assessment of metal fluxes. The sediments of several sites show a significant increase in anthropogenic metal contamination starting from the second decade of last century, with maximum inputs from 1930 to 1970. The decrease of heavy metal concentrations observed in surficial sediments of some sampling sites could be related to a recent reduction of pollutant inputs.     

Partitioning of Cs-137 Between Sediment and Water From the Black Sea

As part of a joint USA/USSR Environmental Agreement to determine the distribution and concentration of Chernobyl radioactivity in the northwest Black Sea area, the sediment from eight stations was collected and analyzed to assess the ability of this material to adsorb radiocaesium. Batch tests were conducted in which Cs-137 tracer was added to mixtures of sediment and bottom water, with contact solutions ranging from 85 Bq ml^-1 to 1,760 Bq ml^-1. This work was done in an argon atmosphere at 9.5°C, which is the average temperature of the sediment. Isotherms were linear for all cores and distribution ratios (R_D) calculated from the slopes of the isotherms ranged from 660 to 1,660 ml g^-1. These isotherms fit a simplified Freundlich isotherm. Correlations of R_D to a number of sediment parameters describing texture and mineralogy were determined. A close relationship was observed between R_D for caesium and the percentage of illite contained in the samples.     

A 50-year sedimentary record of heavy metals and their chemical speciations in the Shuangtaizi River estuary (China): implications for pollution and biodegradation

Two parallel sediment cores collected from tidal flat located in the Shuangtaizi River estuary were analyzed for heavy metal concentrations and chemical speciations. Based on the ¹³⁷Cs activity profile, mean sedimentation rate at the sampling site during the past 50 years was estimated to be 1.3 cm·a^-1. Correlation analyses show that almost all the metals are associated with each other, suggesting that these metals might be derived from same sources and/or affected by same geochemical processes. Influence of total organic carbon (TOC) content on the concentrations of Cr, Ni, Cu and Cd is evident. Silt and clay contents, instead of sand content, play an important role in the distribution of these metals. The dominant binding phases for most of the metals (except for Cd) are the residual. The relative decrease of the residual fraction of Cd and Pb in the upper 66 cm of the core is striking. The distribution of chemical fraction confirms that the residual fractions of these metals have a natural origin, while only the non-residual fractions of Cd and Pb increased upward the core due to pollution in the past five decades. Pollution assessment on these heavy metals based on Index of Geoaccumulation (I_geo) also demonstrates that most of the metals are unpolluted. The weak pollution as observed in the sediments is perhaps related to a local plant, the Suaeda heteroptera Kitag, which may have played a significant role in the biodegradation of these metals and the metal distribution in the estuary.     

Abundance and distribution of ammonia-oxidizing archaea in Tibetan and Yunnan plateau agricultural soils of China

As low oxygen and high ultraviolet （UV） exposure might significantly affect the microbial existence in plateau, it could lead to a specialized microbial community. To determine the abundance and distribution of ammonia-oxidizing archaea （AOA） in agricultural soil of plateau, seven soil samples were collected respectively from farmlands in Tibet and Yunnan cultivating the wheat, highland-barley, and colza, which are located at altitudes of 3200-3800 m above sea level. Quantitative PCR （q-PCR） and clone library targeting on amoA gene were used to quantify the abundances of AOA and ammonia-oxidizing bacteria （AOB）, and characterize the community structures of AOA in the samples. The number of AOA cells （9.34 × 10^7-2.32× 10^8 g^-1 soil） was 3.86-21.84 times greater than that of AOB cells （6.91 × 10^6-1.24 × 10^8 g^-1 soil） in most of the samples, except a soil sample cultivating highland- barley with an AOA/AOB ratio of 0.90. Based Kendall＇s correlation coefficient, no remarkable correlation between AOA abundance and the environmental factor was observed. Additionally, the diversities of AOA community were affected by total nitrogen and organic matter concentration in soils, suggesting that AOA was probably sensitive to several environmental factors, and could adjust its community structure to adapt to the environmental variation while maintaining its abundance.     

Do mucilage events influence pico- and nanoplankton size and structure in the Adriatic sea?

Temporal changes in abundance and biomass of picophytoplankton, heterotrophic pico-eukaryotes, and nanoplankton assemblages were investigated along a transect crossing the Adriatic Sea, from the Italian to the Croatian coast. This 15-months (June 1999-August 2000) investigation allowed comparing microbial parameters during summer 1999 (year without mucilage) and summer 2000 when a major mucilage event occurred. Pico- and nanoplankton assemblages displayed significant differences between the 2 summer periods. The main differences can be summarized as: (i) presence of cyanobacterial blooms (up to 10⁸ cells l^-1) in summer 2000, absent in summer 1999; (ii) an increasing fraction of heterotrophic pico-eukaryotes (up to 5.0 × 10⁶ cells l^-1) and heterotrophic nanoplankton (size 2-5 µm) during mucilage event; (iii) a reduced abundance of small-sized (2-3 µm) phototrophic nanoplankton in summer 2000. Changes in community structure were signals of changes in trophic condition of the system, which resulted in a competitive advantage for small sized pico- and nanoheterotrophs. Data presented here indicated that mucilage events are associated with changes in microbial community structure and functioning in ambient water and induced the amplification of 3-step microbial food chain. The potential use of the heterotrophic pico-eukaryotes for describing alterations of the trophic pathways during mucilage events is discussed.     

渭河流域关中段地表水重金属的污染特征与健康风险评价

由于重金属的毒理性及其对水生生态系统的重要影响,水生环境的重金属污染已成为全世界关注的问题.渭河是黄河的第一大支流,近年来随着沿岸社会经济的发展,渭河的水质受到严重的威胁,但是对渭河流域地表水重金属的污染状况缺乏全面评估.以渭河流域关中段为研究区域,采集了该流域35个地表水样品,检测了12种重金属元素(Cr、Mn、Fe...     

The Freshwater Mussel Parreysia Favidens (Benson) As A Biological Indicator of Polonium - 210 in A Riverine System

The concentration of ²¹⁰Po, an alpha emitter from the natural uranium series was measured in the soft tissues (total), shell, and different organs - digestive glands, gills, mantle and foot - of the freshwater mussel, Parreysia favidens (Benson), collected from the river Kaveri, at Tiruchirapalli in South India. the analyses were made in three size groups based on shell length (Group 1: 2-4 cm; Group 2: 4-5 cm; Group 3: 5-6 cm). the soft tissues of the mussel accumulated higher concentrations of ²¹⁰Po (74.0-125.5 Bq kg^-1 fresh) than the shell (2.9-3.9 Bq kg^-1 fresh). Further, younger mussels (1 group) showed higher concentrations (125.5+2.0 Bq kg^-1 fresh) in total soft tissues than older ones (III Group) (74.0+1.6 Bq kg^-1 fresh); concentration factors were 1.59x 10⁵ in I group and 9.37 × 10⁴ in III group. the ²¹⁰Po was observed to be non-uniformly distributed among the internal organs, which maintained the following descending order with reference to ²¹⁰Po accumulation: digestive glands, ranging from 286.2+3.5 Bq kg^-1 fresh to 43+1.3 Bq kg^-1 fresh. the concentration of ²¹⁰Po in the mussels was distinctly higher than that in the grass, Echinochloa colonum (J. Koenig), and carp, Cirrhinus cirrhosa (Bloch), from the same river. These data indicate that younger mussels could be used as an excellent biological indicator of ²¹⁰Po and among soft tissues, digestive glands are preferable to other tissues to monitor the distribution of ²¹⁰Po in the riverine system.     

Diphenylarsinic acid sorption mechanisms in soils using batch experiments and EXAFS spectroscopy

• DPAA sorption data was found to fit the Freundlich equation. • K_f was significantly positive correlated with oxalate-extractable Fe₂O₃. • Ligand exchange was the main mechanism for DPAA sorption on soils. • Bidentate binuclear and monodentate mononuclear DPAA bonds were identified. Diphenylarsinic acid (DPAA) is a phenyl arsenic compound derived from chemical warfare weapons. Macroscopic and microscopic work on DPAA sorption will provide useful information in predicting the partitioning and mobility of DPAA in the soil-water environment. Here, batch experiments and extended X-ray absorption fine structure (EXAFS) spectroscopy were used to investigate the sorption mechanisms of DPAA. The DPAA sorption data from 11 soil types was found to fit the Freundlich equation, and the sorption capacity, K_f, was significantly and positively correlated with oxalate-extractable Fe₂O₃. The K_f values of eight of the 11 untreated soils (1.51–113.04) significantly decreased upon removal of amorphous metal (hydr)oxides (0.51–13.37). When both amorphous and crystalline metal (hydr)oxides were removed from the untreated soils, the K_f values either decreased or slightly increased (0.65–3.09). Subsequent removal of soil organic matter from these amorphous and crystalline metal (hydr)oxide-depleted samples led to further decreases in K_f to 0.02–1.38, with only one exception (Sulfic Aquic-Orthic Halosols). These findings strongly suggest that ligand exchange reactions with amorphous metal (hydr)oxides contribute most to DPAA sorption on soils. EXAFS data provide further evidence that DPAA primarily formed bidentate binuclear (²C) and monodentate mononuclear (¹V) coring-sharing complexes with As-Fe distances of 3.34 and 3.66 Å, respectively, on Fe (hydr)oxides. Comparison of these results with earlier studies suggests that ²C and ¹V complexes of DPAA may be favored under low and high surface coverages, respectively, with the formation of ¹V bonds possibly conserving the sorption sites or decreasing the steric hindrance derived from phenyl substituents.     

Preliminary Caesium Data From A Cooperative Us/Ussr Monitoring Survey for Chernobyl Radioactivity in the Black Sea

In June 1990, scientists from the US Environmental Protection Agency's (EPA) Office of Radiation Programs (ORP), and the Woods Hole Oceanographic Institution (WHOI), travelled to Sevastopol in the Soviet Union to work with radioecologists and marine scientists from the USSR Institute of Biology of the Southern Seas (IBSS). the purpose of this cooperative programme was to conduct a monitoring survey for radioactivity in the northwestern Black Sea. Samples of sediment, surface and in-situ water, and biota were collected from fourteen stations for post-survey radionuclide analyses to determine levels of radioactivity in the Black Sea environment resulting from the Chernobyl nuclear power plant explosion and subsequent transport of radioactivity via the Dnepr and Danube rivers. This paper presents the preliminary data for caesium-137 and caesium-134 in sediment samples analyzed by the EPA/ORP. Caesium-137 was measured at four shallow (20–114 m) stations on the shelf near the mouth of the Dnepr and Danube Rivers, but was not detected in sediments from comparable depths at stations further off shore or in slope sediments at depths of 510–1288 meters. Caesium-134 was detected only in sediments from the shallow-water station nearest to the Danube River.     

Comprehensive evaluation of heavy metal contamination of sediment in Lake Dianchi by using modified AHP method and Cs dating

Through the use of general sampling and measurement by ¹³⁷ Cs dating, problems regarding the absence of monitoring data can easily be resolved. Further, weighted values need to be determined while Environment Quality Comprehensive Index (EQCI) is commonly used as applied in environmental quality comprehensive evaluation. In order to overcome the subjectivity in determining weights, the modified Analytical Hierarchy Process (AHP) method was designed. The modified AHP method involved the following key procedures: First, the parameters y_i1 and y_i2 were calculated based on the monitoring data; second, the factors were put in order according to the symbol and value of y_i1 and y_i2; third, the continuous odd integers, which represented the importance of factors, were given to factors according to their seating order; and, fourth, the factor weights were determined from the pair-wise comparison matrix calculated by the ratio of the given odd integers. Therefore, the weights were completely based on the monitoring data. In the present study, the comprehensive quality of sediments in five sections of Lake Dianchi were evaluated and the results indicated that the current contamination of sediments in each lake section is much more serious than at any other time in history.     

An improved technique for the determination of organic phosphorus in sediments and soils by 31P nuclear magnetic resonance spectroscopy

Knowledge of organic phosphorus (P) species quantity and distribution in sediments and soils is needed to determine the potential for aquatic and terrestrial organism growth. This can be achieved with ³¹P nuclear magnetic resonance spectroscopy (NMR), but resolving peaks within spectra can be problematic because of broadening via paramagnetics, which can cause peaks to overlap. We compared ³¹P NMR spectra of NaOH-EDTA extracts of three sediments and three soils to those that had first been pre-treated with Ca-EDTA-dithionite to remove Fe and Mn, paramagnetics that cause broadening of peaks, but leave organic P alone. Broadening of peaks in Ca-EDTA-dithionite pre-treated samples decreased by 46% and revealed peaks that were hidden compared to untreated samples. The spectrum of one pre-treated soil was similar if not better than the same soil that had received pre-treatment with Chelex resin (also to remove paramagnetics). Therefore, pre-treatment with Ca-EDTA-dithionite is recommended as a simple and cost-effective method for improving organic P idenTIFication and determination in subsequent NaOH-EDTA extracts of sediments and soils rich in Fe and Mn.     

Light-induced variation in environmentally persistent free radicals and the generation of reactive radical species in humic substances

• Light irradiation increased the concentration of free radicals on HS. • The increased spin densities on HS readily returned back to the original value. • The “unstable” free radicals induced the formation of reactive radical species. • Reactive radicals’ concentration correlated strongly with EPFRs’ concentration. Environmentally persistent free radicals (EPFRs) in humic substances play an essential role in soil geochemical processes. Light is known to induce EPFRs formation for dissolved organic matter in aquatic environments; however, the impacts of light irradiation on the variation of EPFRs in soil humic substances remain unclear. In this study, humic acid, fulvic acid, and humin were extracted from peat soil and then in situ irradiated using simulated sunlight. Electron paramagnetic resonance spectroscopy results showed that with the increasing irradiation time, the spin densities and g-factors of humic substances rapidly increased during the initial 20 min and then gradually reached a plateau. After irradiation for 2h, the maximum spin density levels were up to 1.63 × 10¹⁷, 2.06 × 10¹⁷, and 1.77 × 10¹⁷ spins/g for the humic acid, fulvic acid, and humin, respectively. And the superoxide radicals increased to 1.05 × 10¹⁴–1.46 × 10¹⁴ spins/g while the alkyl radicals increased to 0.47 × 10¹⁴–1.76 × 10¹⁴ spins/g. The light-induced EPFRs were relatively unstable and readily returned back to their original state under dark and oxic conditions. Significant positive correlations were observed between the concentrations of EPFRs and reactive radical species (R² = 0.65–0.98, p<0.05), which suggested that the newly produced EPFRs contributed to the formation of reactive radical species. Our findings indicate that under the irradiation humic substances are likely to be more toxic and reactive in soil due to the formation of EPFRs.