Meiobenthic Organisms as Indicators of Mixing Processes in the Baltic Surface Sediments*

Abstract. Two sediment cores were collected in the southern Baltic Sea and sliced into 1.0cm-thick layers. Sediments of each layer were analysed for activities of ²¹⁰Pb, ¹³⁷Cs, ¹³⁴Cs and for the density of meiobenthic organisms (meiofauna). Zones with the rapid mixing occur in the uppermost layers (0–3 cm) of the cores based on ^I34Cs profiles. The extent and density of meiofauna confirmed the rapid mixing and revealed layers with slow mixing (4–8 cm). Sedimentation rates were derived from ²¹⁰Pb profiles below the mixing zones (1.21 and 1.72 mm a-^I) and were confumed by ¹³⁷Cs distribution. Of twenty-one major meiofauna taxa commonly found in the Baltic sediments, three were present in the cores.     

The history and impact of air pollution at Čertovo Lake,southwestern Czech Republic

This multi-disciplinary investigation documents the longterm effects of atmospheric pollution of metals and acids on a geologically sensitive catchment in the umava Mountains, southwestern Czech Republic, a region with a long history of human disturbance. A 30 cm long sediment core (I) from ertovo Lake was analyzed for natural and artifical radionuclides, metals, diatoms, chrysophytes, and pollen in sediments accumulated during the last 200 years. A second core (II), extending to 95 cm, included sediment judged to be free of atmospheric deposition of pollutants associated with the Industrial Revolution. Chronostratigraphic markers include several changes in the pollen assemblages corresponding to well-documented changes in land-use, and distinct distributions of ¹³⁷Cs, ¹³⁴Cs and ²⁴¹Am from weapons testing and the 1986 nuclear accident at Chernobyl, Russia. These markers corroborate the ²¹⁰Pb dating and, together, produce a reliable chronology extending back nearly to 1800 A.D.Stratigraphic profiles of Cu, Pb, and Zn in Core I are unlike any previously reported in the literature. Concentrations of Cu, Pb, and Zn remain generally above 100, 400, and 200 g g^-1, respectively, for the 200 years represented by Core I. These values are unusually high for sediments from a watershed with no known heavy-metal ore bodies. Accumulation rates for Cu, Pb, and Zn, which include both atmospheric and watershed contributions, are also high (ca 1, > 1 and > 1 g cm^-2 yr^-1, respectively) for the same period, although the anthropogenic contribution of Zn rose from nearly zero at 1800 A.D. The Cu and Pb accumulation rates rose dramatically about 1640 A.D.Accumulation rates of anthropogenically-derived Be, a relatively abundant element in the soft coals of the region, are also elevated by about 0.01 g cm^-2 yr^-1 in sediments of this period. Vanadium accumulation rates increased only since 1980 A.D., presumably along with increased consumption of oil.Diatom assemblages illustrate that the lake was acidic (pH between 4.5 and 5) through at least the past 200 years. The pH declined significantly (from ca 5 to 4) between 1960 and 1985 with a slight increase to 4.5 in the last few years. Recent diatom and chrysophyte assemblages suggest high trace metal concentrations, consistent with the present lake-water chemistry.     

Evaluating the mobility of137Cs,239+240Pu and210Pb from their distributions in laminated lake sediments

Post-depositional mobility of¹³⁷Cs,^239+240Pu and²¹⁰Pb was assessed in six small lake basins by comparing sedimentary nuclide profiles with their known fallout history. Laminae couplets, when present, were determined to be varves because the¹³⁷Cs and^239+240Pu 1963 fallout peaks are present in laminae couplets corresponding to years 1962–1964. There is no evidence of mobility of²¹⁰Pb, because 1) mass accumulation rates based on²¹⁰Pb agree with those based on¹³⁷Cs and^239+240Pu peak depths and with those based on varve counts, and 2)²¹⁰Pb ages agree with varve ages. Significant mobility of¹³⁷Cs is evident from the penetration of¹³⁷Cs to depths 15–20 cm deeper than^239+240Pu. Deep penetration of¹³⁷Cs in spite of a sharp gradient below the peak is interpreted by a numerical model to suggest that¹³⁷Cs is present in two distinct forms in these sediments, 67–82% as an immobile form and 18–33% reversibly adsorbed with a K _d of approximately 5000. The profiles can be interpreted equally well assuming a small portionof the total¹³⁷Cs was present as an extremely mobile phase (K _d 5000) in the months to years following peak fallout, slowly becoming more strongly adsorbed. High NH ₄ ⁺ concentrations in porewaters may enhance diffusion of the mobile form of¹³⁷Cs, but not of the immobile form of¹³⁷Cs that defines the sharp gradient. Mobility of¹³⁷Cs is likely also enhanced by the low clay content and the high porosity of these sediments. Thus the first detection of¹³⁷Cs in the sediments cannot automatically be assumed to correspond to a date of 1952 (initial testing of thermonuclear weapons), although the depth of the peak can be assumed to correspond to 1963 (the year of maximum fallout from testing of thermonuclear weapons).^239+240Pu is a more reliable sediment chronometer than¹³⁷Cs because it is significantly less mobile.This is the sixth of a series of papers to be published by this journal following the 20 ^th anniversary of the first application of²¹⁰Pb dating of lake sediments. Dr P.G. Appleby is guest editing this series.     

Analysis of Karst Tufa from Guangxi, China

The paper presents an analysis of characteristic karst tufa from Guangxi, China, which has not been studied before. A comparison with tufa from Dinaric Karst of Croatia is discussed in view of the C-type climate. The major mineral is calcite. Minor minerals are quartz and dolomite, depending on location. The content of calcium carbonate varies from 65% to 92%, and that of magnesium carbonate from 0.03% to 1.77%. Among other elements, the most abundant are Fe, from 0.02% to 1.50%, and Ti, from 0.15% to 0.27%. Many other trace elements (V, Cr, Mn, Ni, Cu, Zn, As, Se, Br, Rb, Sr, Y, Zr, Hg and Pb) are also present. Specific activity of radionuclides 40K, 232Th, 137Cs, 226Ra and 238U varies from sample to sample. Concentration of U in tufa is close to that reported for sedimentary carbonate. Low concentration of 137Cs indicates that this part of the world was not exposed to nuclear explosions. The concentration of 226Ra is the highest in Mashan County. The ratio 238U/226Ra (0.21-0.71) in tufa from Mashan Co     

Erosion rates of alpine bedrock summit surfaces deduced from in situ Be and Al

We have measured the concentration of in situ produced cosmogenic ¹⁰Be and ²⁶Al from bare bedrock surfaces on summit flats in four western U.S. mountain ranges. The maximum mean bare-bedrock erosion rate from these alpine environments is 7.6 ± 3.9 m My⁻¹. Individual measurements vary between 2 and 19 m My⁻¹. These erosion rates are similar to previous cosmogenic radionuclide (CRN) erosion rates measured in other environments, except for those from extremely arid regions. This indicates that bare bedrock is not weathered into transportable material more rapidly in alpine environments than in other environments, even though frost weathering should be intense in these areas. Our CRN-deduced point measurements of bedrock erosion are slower than typical basin-averaged denudation rates ( 50 m My⁻¹). If our measured CRN erosion rates are accurate indicators of the rate at which summit flats are lowered by erosion, then relief in the mountain ranges examined here is probably increasing.

We develop a model of outcrop erosion to investigate the magnitude of errors associated with applying the steady-state erosion model to episodically eroding outcrops. Our simulations show that interpreting measurements with the steady-state erosion model can yield erosion rates which are either greater or less than the actual long-term mean erosion rate. While errors resulting from episodic erosion are potentially greater than both measurement and production rate errors for single samples, the mean value of many steady-state erosion rate measurements provides a much better estimate of the long-term erosion rate.     

南极长城站附近企鹅栖息地粪土沉积地层放射性核素210Pb定年

用γ谱方法测定了南极长城站附近特有生物群落栖息地沉积物中放射性核素含量,地表沉积物中40K,137Cs,210Pb,226Ra,228Ra,228Th.和238U平均比活度,分别为143,7.56,24.1,3.65,5.36,4.15和6.5Bq/kg.同时测试了阿德雷岛企鹅栖息地粪土沉积地层中放射性核素含量,利用其中的210Pb比活度,210Pb_ex垂向变化特征,推演沉积物的沉积速率和地质历史年代:其中AD1-a柱样时间跨度约为74a(1928~2002年),据此计算了沉积速率为0.063mm/a(r=0.794),并讨论了在南极特定条件下,放射性核素示踪对定年影响以及与区域现代气候环境变化的内在联系.     

Gamma Emitters on Micro-Becquerel Activity Level in Air at Kraków (Poland)

The Petryanov air filters combined into half-year sets were analyzed for the presence of ⁴⁰K, ¹³⁷Cs and ²²Na by means of low-background gamma rays spectrometry. Each sample contains aerosols from more than 1 Mm³ of air. Samples were collected in ground level air at Kraków (Southern Poland) from 1996 to 2002. Activity concentrations of ⁴⁰K are almost constant with the mean of 14.7± 4.5 Bq m^–3. Activity concentrations of ¹³⁷Cs, which are on the level of single Bq m^{– 3} show exponential decrease with effective half-life time of 7.07± 0.77 years. The cosmogenic ²²Na shows a strong seasonal variation with significant different mean values activity concentration between 0.333± 0.095 Bq m^–3 and 0.137± 0.045 Bq m^–3, for summer and winter, respectively. Moreover, the activity ratio for two cosmogenic radionuclides: ²²Na and measured previously ⁷Be show also changes with statistically significant seasonal differences. The lower values were found during winters. The mechanisms which might govern this ratio are discussed. The conclusion is that transport of ²²Na during summer seems to be so much effective, that results in kind of relative depletion of stratosphere of this nuclide.     

太阳系早期的短寿期放射性核素

较详细地介绍全新的太阳系起源理论——X-wind模式,天体化学实验发现太阳系早期存在大量的短寿期放射性核素(半衰期小于100Ma),这些核素对太阳系的形成和演化有重要的影响,一种理论认为,这些核素是在恒星内部合成,并由星风注入原太阳分子云,星风产生的激波诱发分子云核的塌缩而形成原太阳,另一种理论认为,这些核素是高能粒子与原太阳分子云或太阳星云中的气体和尘埃相互作用的产物。     

历次核试验进入海洋的~(137)Cs对中国近海影响的模拟研究

1945年以来,世界各主要核国家进行了数千次核试验,这些核试验产生的绝大部分放射性物质通过多种途径进入海洋,对海洋环境造成放射性污染。本文建立了一个准全球海洋的放射性物质输运和扩散数值模式,通过数值模拟手段评估了历史核试验释放的放射性物质137 Cs对中国近海海洋环境的影响。本文借助前人工作评估了核试验释放137Cs进入海洋的途径和总量;通过比较模拟结果与观测资料,表明本文建立的放射性物质模式能够较好地模拟出137Cs在中国近海及其邻近海域的分布情况和随时间演变特征;模拟结果表明中国近海里的137Cs浓度在20世纪50年代中期达到最大,其中吕宋海峡海域137Cs浓度最高,达80.99Bq/m3;进一步分析了2011年3月份日本福岛核事故前中国近海137Cs浓度分布状况,2011年整个中国近海137Cs浓度介于1.0~1.6Bq/m3间,且其浓度垂向分布较均匀,相对封闭的南海浓度略高于其他海域。