Comparative Estimation of the Plutonium (238Pu, 239+240Pu) and Radiocesium (137Cs) Content in Bottom Sediments and Hydrobionts of the Yenisei River

Doklady Earth Sciences - The contents of isotopes of plutonium (238Pu and 239, 240Pu) and 137Cs in samples of bottom sediments and hydrobionts (water moss, amphipods, and caddisfly larvae with...     

Plutonium, 241Am and 137Cs ratios,inventories and vertical profiles in Washington and Oregon continental shelf sediments

Continental shelf sediments from nine locations off Washington and Oregon have ^239,240Pu inventories which average 8.0 ± 2.6 mCi/km². The Columbia River and seawaters advecting over the shelf supply Pu which is removed to underlying sediments, principally through scavenging by inorganic paniculate matter. Mass balance calculations argue that less than 20 percent of the advected Pu need be scavenged from the water column to balance river input and total shelf sediment inventories. The percentage of the Pu removed through scavenging is consistent with observed participate concentrations in shelf waters and published sediment/water distribution coefficients.No marked separation of Pu from ¹³⁷Cs is observed with depth in Pacific shelf sediments as has been reported in Atlantic coastal sediments. This interocean distinctness can be explained by differences in particle mixing and downward diffusion of Cs in sediments of varying porosities. The transuranic inventories and Pu/Cs ratios in the Pacific sediments do not support the hypothesis of Livingston and Bowen that Pu is remobilized within the sediment column by ‘complexone’ formation with (principally) organic substances.Excess ²¹⁰Pb/^239,240Pu inventory ratios in eight representative cores from the Washington shelf average 100 ± 19, even though absolute values of both inventories vary by much larger factors. This reasonably constant ratio, for a given water depth, permits estimation of total Pu inventories and prediction of sites of unusual Pu accumulation from data on the more easily measured natural radionuclide.     

Determination of 210Pb, 226Ra and 137Cs in sediments

A method is described for bringing a sediment sample into solution and subsequently carrying out analysis for ²¹⁰Pb, ²²⁶Ra and ¹³⁷Cs. Silica is removed from the sample by cyclic HNO₃HF treatments. ¹³⁷Cs is separated from ²¹⁰Ra in a carbonate fusion, extracted by absorption on ammonium molybdophosphate, precipitated directly with BiI₃ in presence of citric acid, and β-counted. ²¹⁰Pb and ²²⁶Ra are separated out by 70–75% HNO³ precipitation. Further purification and mutual separation of the two radionuclides is achieved by solvent extraction and anion-exchange techniques. ²¹⁰Pb and ²²⁶Ra are determined by β- and α- counting of their chromate precipitates, respectively, after allowing suitable ingrowth periods for their daughters. The procedural steps effectively eliminate possible interference from other natural or fall-out radioactivities.     

天津三河岛潮间带137Cs与210Pb的分布及现代沉积过程

位于永定新河、潮白新河与蓟运河汇流处的三河岛是天津市列入国家海岛名录的唯一岛屿,其独特的地理位置记录了现代海、陆交互作用的变化过程。取自该岛南、北两侧泥质潮间带的2组现代沉积物样柱,揭示137Cs和210Pbexc的最大检出深度分别达到90～123cm和140～210cm,属于渤海湾西岸泥质海岸带现代沉积最为活跃的“面向开放海湾亚带”。     

Atmospheric pollutants transport tracks revealed from 131I, 137Cs,and 134Cs leaked from Fukushima accident and 7Be and 210Pb observed at Guiyang of China

A massive earthquake measuring 9.0 on the Richter scale that occurred on March 11, 2011, on Honshu Island, Japan, caused radioactivity leakage from the Fukushima Nuclear Power Plant, which led to the leakage of artificial nuclides （131I, 137Cs, and 134Cs） and their global transportation by atmospheric circulation. This paper re- ports a systematic comparative observation on radioactive concentrations of natural nuclides （7Be and 210Pb） and artificial nuclides （131I, 137Cs, and 134Cs） at the surface level, measured in weekly continuous aerosol sampling at Mount Guanfeng, Guiyang, China, from March 17, 2011 to April 28, 2011. During this period, the variations in the nuclide concentrations associated with their transport paths were analyzed with 315 hour back-trajectories of air mass initialized 500 m above the surface level at Guiyang. The results show that the pollutants of nuclear leakage from the Fukushima accident were transported to the Guiyang region of China via two significant pathways. In the first pathway the first wave of nuclear pollutants were transported from west to east in air masses at higher altitudes via global atmospheric circulation. The nuclear pollutants encircled the Earth almost once and after about 10 days to two weeks, between March 24 and March 31,2011, intruded Guiyang from the northwestern region of China. In the second pathway, the nuclear pollutants from the Fukushima region arrived at Guiyang between April 7 and April 14, 201 l, via air masses at lower altitudes that moved southwards because of the squeezing of the northeast Asian weather system and then by the influence, in succession, of the northeastern and southeastern air currents in the low-latitude region. The first transport pathway for atmospheric pollutants is on a global scale and based on air masses at higher altitudes, and the second transport pathway is on an eastern Asia regional scale and based on the air masses at lower altitude.     

The relative mobility of natural (Th,Pb and Po) and fallout (Pu,Am, Cs) radionuclides in the coastal marine environment: results from model ecosystems (MERL) and Narragansett Bay

The relative mobility of nuclides of Pb, Th, Pu, and Cs, which are widely used as geochemical tracers for sedimentation and bioturbation. was investigated in artificial microcosm tanks (MERL) and in Narragansett Bay. Their mobility was characterized by their removal rates from the water column, their affinity toward particles and their degree of penetration into the surface sediments. Pb, Th, and Pu transport was controlled predominantly by the affinity of these elements to particles, and the transport parameters of the particles themselves (i.e. sediment resuspension and mixing rates). Because of its low distribution coefficient, transport of Cs was controlled by molecular diffusion through pore water in the winter, while in summer, Cs transport was enhanced due to bioturbation. The increase with depth of the $\text{Cs}\text{Pu}$ ratio in core profiles of MERL and Narragansett Bay sediments is thus caused primarily by the higher mobility of Cs.     

137Cs剖面的沉积信息提取——以香港贝澳湿地为例

通过建立模型,对采自香港大屿山岛贝澳湿地三个站位的沉积样品的137Cs实测剖面与模型计算剖面的比较分析,得出三个站位的沉积速率分别为0.24 cm/a、0.21 cm/a、0.34 cm/a,除P1站位外,P2、P3站位由于受到潮水的作用,表层沉积物受到侵蚀,侵蚀量分别为4.8 cm和7 cm。该结果与常用的时标方法所的结果进行了比较,P1站位由上述模型所得的结果与常用的时标方法所得的结果一致。可以看出,在稳定的沉积环境下,常用的确定时标的方法可以较准确地计算出沉积速率,而在堆积与侵蚀变化的沉积环境下,常用的确定时标的方法就存在一定的缺陷。该工作为137Cs剖面的沉积信息提取进行了有益的尝试。但上述模型中,由于采用日本东京地区的137Cs大气沉降通量记录替代香港地区的137Cs大气沉降通量记录,并没有考虑 137Cs的扩散效应,所以该模型还有待进一步的改进。     

桂西北典型岩溶区水稻田成土剖面砷的垂向分布特征及其影响因素

调查分析桂西北典型岩溶矿区及其周边水稻田成土剖面砷含量及相关土壤参数垂向分布特征,研究了岩溶区土壤砷的含量垂向分布及迁移规律,并探讨了岩溶区土壤砷垂向迁移的主要影响因素。结果表明:研究区三个典型土壤剖面的主要土壤类型为石灰岩土,化学风化程度较高,土壤砷自然来源主要为土壤母质;土壤剖面砷含量的垂向分布均为表层相对富集、深层相对稳定,而土壤有机碳是制约岩溶区水稻田土壤砷垂向迁移的关键因素;矿区外围的两个土壤剖面砷含量主要富集在10～20 cm层,而在0～10 cm层砷含量相对较低,土壤砷含量平均值分别为5.5 mg·kg-1 和5.0 mg·kg-1 ;而临近矿区的土壤剖面具有土壤砷高背景值的特点,土壤砷含量平均值为46.2 mg·kg-1 ,且砷主要富集在20～40 cm的次表层,而在10~20 cm层砷含量则相对较低,但在0～10 cm层土壤砷含量又显著高于10～20 cm层,这表明外来源对该剖面表层土壤也具有显著影响。      

Recommended Values of 239Pu, 240Pu and 239+240Pu Concentrations in Reference Material IAEA-315 (Marine Sediment) Estimated by Thermal Ionisation Mass Spectrometry, Inductively Coupled Plasma-Mass Spectrometry and Alpha Spectrometry

The recommended concentrations of ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu in reference material IAEA‐315 (marine sediment) were estimated by three analytical methods: isotope dilution thermal ionisation mass spectrometry (TIMS), isotope dilution inductively coupled plasma‐mass spectrometry (ICP‐MS) and alpha spectrometry. The determination of ²³⁹Pu and ²⁴⁰Pu (^239+240Pu by alpha spectrometry) was carried out with samples from randomly selected bottles using each method. Plutonium‐238 was also measured by alpha spectrometry. A plutonium‐242 reference material was used as a spike for the quantitative analysis. The influence of ²⁴²Pu in the samples was therefore calculated; however, this contribution was less than the range of uncertainty and did not influence the final results. The obtained data were statistically analysed using variance component analysis and paired comparison. The combined standard uncertainties from “method/measurement”, “bottle” and “sub‐sample” were in the order of 3 to 6%. The main contributions to the uncertainty were from the material heterogeneity and from systematic differences between methods. Based on this study with twenty‐seven analyses using 10–14 g sample mass, concentrations of (38 ± 3) Bq kg^?1, (28 ± 3) Bq kg^?1 and (66 ± 4) Bq kg^?1 are proposed as recommended values for ²³⁹Pu, ²⁴⁰Pu and ^239+240Pu, respectively, and (9.5 ± 0.4) Bq kg^?1 for ²³⁸Pu as an information value in reference material IAEA‐315. In mass concentration units, these amount to (16.4 ± 1.2) ng kg^?1, (3.3 ± 0.4) ng kg^?1 and (0.015 ± 0.003) ng kg^?1 for ²³⁹Pu, ²⁴⁰Pu and ²³⁸Pu, respectively. The certified reference materials NIST 4350B and NIST 4354 were also analysed by TIMS for quality assurance of the method used in this study.     

Determination of 137Cs activities in surface sediments and derived sediment accumulation rates in Thessaloniki Gulf, Greece

Surficial and core samples collected from the eastern Thessaloniki Gulf, located in the NW Aegean Sea, were analyzed for their sedimentation rate and inventories of ¹³⁷Cs and ²¹⁰Pb. The study of the spatial radionuclide dispersion in the specific region is essential for the assessment of marine pollution levels. The sedimentation rates were calculated from the vertical distribution of ¹³⁷Cs and excess ²¹⁰Pb in the sediment cores. The spatial distribution of ¹³⁷Cs was studied with respect to sediment characteristics such as the grain size of the sample and the organic carbon content. The activity concentrations were measured by means of gamma ray spectrometry using HPGe detector for ¹³⁷Cs and gross alpha counting using alpha counter for ²¹⁰Pb. The average sedimentation rate along the sediment cores is characterized by a consistent pattern and varies from 0.18?±?0.02 to 0.22?±?0.03?cm?year^?1. The ¹³⁷Cs inventories varied from 205?±?15 to 602?±?39?Bq?m^?2, while the ²¹⁰Pb inventories of the studied cores exhibited average value of 140?±?9?Bq?m^?2. Elevated ¹³⁷Cs activities were observed compared to certain Mediterranean marine areas; however, they were lower than the reported values in the Black Sea.     

Use of fallout 137Cs for documenting the chronology of overbank sediments from the river Sava, Croatia, and interpreting their geochemical patterns

This paper attempts to determine the impact of former Pb-Zn-Ba mining activities in Slovenian drainage basin on overbank sediments of the Sava river (West Croatia). Among the four studied sequences (S7, S8, S9, S10), the most upstream profile S7 showed the most pronounced impact of ore mining. Mercury was enriched more than 100-fold; Pb and Zn had a strong positive correlation (r > 0.99). Two factor models clearly revealed the Pb-Ba-Hg association in the lower-lying carbonate (CA) population of all four profiles, but only in the overlying silicate (SI) population of profile S7. Factor analysis confirmed this association in the total sediment (90 samples) as well as separately in the CA (33 samples) and SI (57 samples) populations. Based on a comparison with an undisturbed soil profile, the vertical distribution of ¹³⁷Cs in profile S7 was interpreted to be the combination of caesium deposition caused by a flood in 1964 and by post-depositional redistribution.     

雄安新区土壤重金属和砷元素空间分布特征及源解析

研究雄安地区土壤重金属和砷元素空间分布特征及其来源,对于支撑新区土地资源和环境管理具有重要意义。基于雄安新区土壤环境调查,运用地统计学方法和ArcGIS 技术分析模拟了土壤中As、Hg、Cd、Cu、Pb、Zn、Ni、Cr等8种元素空间分布特征,综合运用空间分析、多元统计学方法和正定因子矩阵模型解析这些元素的主要来源。结果表明：（1）区内土壤质量总体良好,4.35 %的土壤样品Cd和Cu含量超过农用地土壤污染风险筛选值,但均低于农用地土壤污染风险管控值;与河北省背景值相比,Cd、Cu、Pb、Zn和Hg存在不同程度中度和显著富集。（2）As、Cd、Cu、Pb、Zn、Ni、Cr含量呈现出由北部向南部逐渐增高的趋势,高值区主要分布在新区西南部;Hg元素分布分散,高值区主要分布在城镇及工业企业周边。（3）不同土地利用类型土壤剖面重金属和砷元素垂向分布受pH值、有机碳和铁铝氧化物等理化性质影响显著。（4）研究区土壤重金属和砷元素富集受人类活动影响明显,人为来源贡献率达67.12 %,Hg元素主要来源于人为排放的大气沉降富集,As元素富集受到废渣堆放和利用的影响,Cd、Cu、Pb和Zn元素富集受工业生产、污水灌溉以及尾气排放等活动影响。研究成果可为雄安新区合理制定土地资源开发利用和生态保护措施提供技术支撑。     

Mechanisms and Sources of Mantle Metasomatism: Major and Trace Element Compositions of Peridotite Xenoliths from Spitsbergen in the Context of Numerical Modelling

Mineral and whole-rock chemical data for peridotite xenolithsin basaltic lavas on Spitsbergen are examined to reassess mechanismsof melt–fluid interaction with peridotites and their relativerole versus melt composition in mantle metasomatism. The enrichmentpatterns in the xenoliths on primitive mantle-normalized diagramsrange from Th–La–Ce ‘inflections’ inweakly metasomatized samples (normally without amphibole) toa continuous increase in abundances from Ho to Ce typical foramphibole-bearing xenoliths. Numerical modelling of interactionbetween depleted peridotites and enriched melts indicates thatthese patterns do not result from simple mixing of the two end-membersbut can be explained by chromatographic fractionation duringreactive porous melt flow, which produces a variety of enrichmentpatterns in a single event. Many metasomatized xenoliths havenegative high field strength element and Pb anomalies and Srspikes relative to rare earth elements of similar compatibility,and highly fractionated Nb/Ta and Zr/Hf. Although amphiboleprecipitation can produce Nb–Ta anomalies, some of thesefeatures cannot be attributed to percolation-related fractionationalone and have to be a signature of the initial melt (possiblycarbonate rich). In general, chemical and mineralogical fingerprintsof a metasomatic medium are strongest near its source (e.g.a vein) whereas element patterns farther in the metasomatic‘column’ are increasingly controlled by fractionationmechanisms. KEY WORDS: Spitsbergen; lithospheric mantle; metasomatism; trace elements; theoretical modelling     

Geochronology of a surface core in the northern basin of Lake Qinghai： Evidence from ^210pb and ^137Cs radionuclides

1 Introduction The radionuclides 210Pb and 137Cs are of particularimportance for estimating the dates of recentsediments. It was Goldberg (1963) who firstlysuggested that the disequilibrium between 210Pb and226Ra could serve as a geochronometer applicable…     

Deformation microstructures of olivine in peridotite from Spitsbergen, Svalbard and implications for seismic anisotropy

To understand the deformation mechanism and seismic anisotropy in the uppermost mantle beneath Spitsbergen, Svalbard, in the Arctic, the deformation microstructures of olivine in the peridotite of Spitsbergen were studied. Seismic anisotropy in the upper mantle can be explained mainly by the lattice-preferred orientation (LPO) of olivine. The LPOs of the olivine in the peridotites were determined using electron backscattered diffraction patterns. Eight specimens out of 10 showed that the [100] axis of the olivine was aligned subparallel to the lineation and that the (010) plane was subparallel to the foliation, showing a type A LPO. In the other two specimens the [100] axis of olivine was aligned subparallel to the lineation and both the [010] and [001] axes were distributed in a girdle nearly perpendicular to the lineation, showing a type D LPO. The dislocation density of the olivine in the samples showing a type D LPO was higher than that in the samples showing a type A LPO. The result of an Fourier transformation infrared study showed that both the types A and D samples were dry. These observations were in good agreement with a previous experimental study ( Tectonophysics , 421 , 2006, 1 ): samples showing a type D LPO for olivine were observed at a high stress condition and samples showing both types A and D LPO were deformed under dry condition. Observations of both strong LPOs and dislocations of olivine indicate that the peridotites studied were deformed by dislocation creep. The seismic anisotropy calculated from the LPOs of the olivine could be used to explain the seismic anisotropy of P - and S -waves in the lithospheric mantle beneath Spitsbergen, Svalbard.     

散落核素7Be和137Cs在洱海和红枫湖沉积物中蓄积对比

沉积物柱芯分别采自滇西地区的洱海和黔中地区的红枫(及百花)湖,散落核素7Be和137Cs在沉积物中的蓄积特征对比分析表明,7Be在洱海及红枫湖沉积物中的累计值分别为(237±73)Bq/m2和(783±44)Bq/m2;按校正到沉降年代的数值,1986年以前137Cs的累计值分别为(519±26)Bq/m2及(3704±56)Bq/m2.由模式计算获知,(1)7Be和137Cs在红枫湖沉积物中的蓄积以侵蚀影响为主;在洱海的蓄积受直接散落控制.(2)在洱海和红枫湖地区7Be大气散落累计值分别为(0.07±0.02)Bq/cm2及(0.08±0.01)Bq/cm2;1986年以前137Cs大气散落累计值分别为(0.11±0.01)Bq/cm2及(0.37±0.01)Bq/cm2,显示出滇西与黔中地区之间137Cs散落的地区差异.这一现象可能反映出青藏高原对滇西地区存在着全球性大气扩散污染物散落的屏蔽效应.