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.     

Dating recent colluvial sequences with Pb and Cs along an active fault scarp, the Eliki Fault, Gulf of Corinth, Greece

Reliable dating is an essential element of palaeoseismological studies, yet whilst a suite of geochronological methods can now provide late Quaternary age control it remains very difficult to date modern events (i.e., those occurring within the last 150 years). This is significant because the starting point for many palaeoseismological investigations is a modern surface-rupturing event, whose geological effects need to be disentangled in trench stratigraphies from palaeoseismic ruptures. Two dating methods which, in combination, can provide robust dating control in recently deposited sediments are the ²¹⁰Pb and ¹³⁷Cs dating methods. Here, we test the applicability of using ²¹⁰Pb and ¹³⁷Cs to date colluvial sediments exposed in three trenches excavated across an earthquake fault—the Eliki fault, Gulf of Corinth, Greece—which ruptured in an earthquake in 1861. The ²¹⁰Pb and ¹³⁷Cs profiles observed in these colluvial sequences are relatively erratic due to the mixed nature of the sediments, i.e., their deposition in an environment where the supply of slope sediments is driven by seasonal rainfall, causing non-uniform sediment accretion and sediment reworking. In one trench, however, ²¹⁰Pb dating, corroborated by ¹³⁷Cs dating, indicates that a proposed post-1861 surface colluvial unit has been deposited over the period 1950 AD–present (at a rate of ca. 9 mm/year), and overlies a significantly older unit (>120 years old). The dating control provided here by ²¹⁰Pb and ¹³⁷Cs dating corroborates the published interpretation of the trench stratigraphy, and refines the ¹⁴C-based estimated dates for the upper unit. At two other trenches ²¹⁰Pb and ¹³⁷Cs dating only provided minimum ages (based on the presence or absence of ²¹⁰Pb_excess and ¹³⁷Cs). Such approximate ages, however, may still useful in corroborating interpretations made using the trench stratigraphy, or, at sites which have long earthquake recurrence intervals, determining which earthquake event was responsible for a particular bed offset.     

High-resolution historical records from Pettaquamscutt River basin sediments: 1. Pb and varve chronologies validate record of Cs released by the Chernobyl accident

Cesium-137 derived from the explosion of the Chernobyl reactor in 1986 was preserved in anoxic sediments from a coastal environment in southern Rhode Island. Although the radioactive plume was detected in surface air samples at several locations in the United States, this is the first known record of a Chernobyl ¹³⁷Cs peak in sediments from North America. The inventory of Chernobyl ¹³⁷Cs that was preserved in the Pettaquamscutt River is small compared to European counterparts and should only be detectable for the next 15-20 yr. However, the presence of two ¹³⁷Cs peaks (1963 and 1987) identifies a well-dated segment of the sediment column that could be exploited in understanding the decomposition and preservation of terrestrial and aquatic organic matter. Different methods for calculating the ²¹⁰Pb chronology were also evaluated in this study and checked against independent varve counting. The end result is a detailed chronology of a site well suited for reconstruction of historical records of environmental change.     

Estimate of the density of global fallout of cesium-137 according to the data of its content in closed geochemical arenas of southwestern Siberia

The density of global radioactive contamination was the most reliable estimated in marine regions and less accurate for intracontinental areas with semi-arid and arid climatic conditions. This work presents the results of using a new method developed for estimating the density of global radioactive contamination based on the calculation of ¹³⁷Cs concentration in closed lake catchments. An average density of of ¹³⁷Cs contamination in the model closed lake catchments of southwestern Siberian steppe landscapes is 0.80 ± 0.24 kBq m^–2 that is 2–3 times lower than the levels calculated on the basis of the published data.     

Ice accumulation rate in Changme-Khangpu glacier,Sikkim

Vertical profiles of¹³⁷Cs and²¹⁰Pb have been determined in a 9 m column of ice from accumulation zone of Changme-Khangpu glacier in north Sikkim valley.¹³⁷Cs activity varies from 4 to 22 dpm/ L. In many samples²¹⁰Pb occurs at a level of 20 to 65 dpm/ L which is much higher than the expected fallout value.¹³⁷Cs and²¹⁰Pb activities correlate well with each other but not with the dust content. Possibility of²¹⁰Pb production in the nuclear explosions is discussed. Several peaks appear in the depth profile of¹³⁷Cs and²¹⁰Pb which can be matched with Chinese atmospheric nuclear explosions with some phase difference if a uniform ice accumulation rate of 0.7 m per year is assumed since 1969.     

Reversible ion-exchange fixation of cesium-137 leading to mobilization from reservoir sediments

The radioactive fission product, ¹³⁷Cs, has been observed to mobilize from bottom sediments of two South Carolina reservoirs during summer thermal stratification and hypolimnetic anoxia. Mobilization is attributed to ion-exchange displacement of ¹³⁷Cs from sediments by cations such as NH⁺₄, Fe⁺² and Mn⁺² released under anaerobic conditions.Three types of ¹³⁷Cs binding sites to sediment clay minerals are identified: 1) surface and planar sites from which ¹³⁷Cs is generally exchangeable by all cations studied (Na⁺, NH⁺₄, H⁺, Cs⁺, Ca⁺², Mg⁺², Fe⁺², and Mn⁺²); 2) wedge sites where ¹³⁷Cs exchange is sterically limited to cations of similar size and charge (NH⁺₄, Cs⁺, K⁺, and perhaps H₃O⁺); 3) interlayer sites from which ¹³⁷Cs is not readily exchanged. More than 15 years after final ¹³⁷Cs inputs, the reservoir sediments we studied showed the following percentage distribution of sites: 2 to 9% surface sites, 6 to 13% wedge sites, and 78 to 85% interlayer sites. In contrast, lake and stream sediments near Oak Ridge, Tennessee receiving ¹³⁷Cs inputs more than 20 years earlier had greater than 99% of their ¹³⁷Cs associated with non-exchangeable interlayer sites. The difference is attributed to the paucity in the South Carolina sediments of weathered micaceous clay minerals with their abundant interlayer sites. Such interlayer deficient clays are dominant in the Atlantic and Gulf coastal plains of the United States and elsewhere. This suggests that ¹³⁷Cs will be physically and chemically more mobile in such areas as well as more biologically available. Mobility will be enhanced in regimes where cation inputs favoring ¹³⁷Cs exchange occur. Subsurface waste disposal sites where anaerobic conditions develop with NH⁺₄ production and Fe⁺² and Mn⁺² release might be such a regime.     

An analysis of naturally occurring radionuclides and <Superscript>137</Superscript>Cs in the soils of urban areas using gamma-ray spectrometry

This study of environmental radioactivity was carried out in the soils of an urban area. Naturally occurring gamma-emitting radionuclides and man-made ¹³⁷Cs were found in the soil profiles collected from four parks in the central Belgrade city area and the soil layer was examined every 10 cm and to a depth of 50 cm. Radioisotope activity concentrations (Bq kg^?1) in the samples of urban soil using the gamma-ray spectrometry method were in the range of 14–46 for ²³⁸U, 33–50 for ²²⁶Ra, 29–63 for ²¹⁰Pb, 1.2–3.4 for ²³⁵U, 28–50 for ²³²Th, 424–576 for ⁴⁰K and 0.7–35.8 for ¹³⁷Cs. Some of the basic physicochemical soil properties (pH, organic matter content, calcium-carbonate content, particle size distribution) were determined to investigate the impact on the vertical distribution of radionuclides. The results of this investigation showed that variations of activity concentration ratios of radionuclides that belong to the same (²³⁸U/²²⁶Ra) or different radioactive series (²³²Th/²²⁶Ra; ²³⁵U/²³⁸U), including ²¹⁰Pb/¹³⁷Cs ratios could well be explained by the properties of the soil. Alkaline pH reaction, the accumulation of organic matter in the uppermost and of carbonates in the deepest layers of urban soil had an effect on ²³⁸U/²²⁶Ra, and ²¹⁰Pb/¹³⁷Cs activity concentration ratio values, while ²³²Th/²²⁶Ra and partially ²³⁵U/²³⁸U ratios were associated with the particle sizes vertical distribution. A study of radionuclides in the samples of leaves of two deciduous tree species common for these parks was also conducted and ²¹⁰Pb and ⁴⁰K were found concentrated in leaves rather than other investigated radionuclides.     

放射性同位素定年技术在崇明岛潮滩沉积速率上的应用研究

选取崇明岛北侧由东至西4个潮滩沉积柱,分析137Cs、226Ra和210Pb放射性比活度,应用210Pb和137Cs放射性同位素定年方法计算崇明岛潮滩沉积物沉积速率。对于东西两端,210Pb方法测得速率分别为3.08cm/a和2.34 cm/a,而137Cs测得速率分别为6.19 cm/a和2.06 cm/a。结果表明,137Cs定年方法计算出的潮滩沉积速率普遍大于210Pb方法结果;但两者反映了相同的速率规律。崇明岛主力生长方向为东和东北,西侧沉积作用相对较弱,表现出"东快西慢"的特点。沉积纵向上,1954年以来,自下而上沉积速率逐渐减缓。     

Lead-210 sediment geochronology in a changing coastal environment

Sediment accumulation rate studies utilizing excess ²¹⁰Pb and ¹³⁷Cs were conducted as part of recent investigations of biogeochemical cycling at a single site in Cape Lookout Bight, a rapidly changing coastal basin on the Outer Banks of North Carolina (U.S.A.). Cores three meters in length reveal a depositional history for the bight interior characterized by a gradual transition in texture from coarse-grained to fine-grained material over the period 1946–1979. This transition is controlled by progressive enclosure of the bight by an active northerly migrating recurved spit. The textural gradation is periodically interrupted by layers of well-sorted sand associated with major storm events. Lead-210 data indicate that the upper meter of the sediment has accumulated at a rate of 3.35 to 4.71 g · cm^?2 · yr^?1 or approximately 8.4 to 11.8 cm · yr^?1 (at ø = 0.84). Below 120 cm depth, dilution of clay and silt by low activity sand necessitates correction of the ²¹⁰Pb profile in order to establish a geochronology. Grain size ²¹⁰Pb distribution measurements at three depths reveal that the specific activity (dpm · g^?1) of clay is 3.2 times that of silt and 24.7 times that of sand. Corrections of bulk sediment excess ²¹⁰Pb activities based on these measurements lead to dates for textural changes which are consistent with charted changes in basin morphology and major storm events.Sixteen ¹³⁷Cs measurements between 33–241 cm depth reveal a peak activity at 105–115 cm and indicate a minimum sedimentation rate of approximately 2.7 g · cm^?2 · yr^?1.     

Tracing depositional consequences of environmental radionuclides (137Cs and 210Pb) in Slovenian forest soils

Depth distribution profiles of environmental radionuclides (¹³⁷Cs and ²¹⁰Pb) have been investigated in soil to elucidate the underlying environment of semi-natural temperate deciduous and/or coniferous forest soils in Slovenia (?irovski vrh, Idrija, Ko?evski Rog, Pohorie, Gori?nica and Rakitna). Surface enrichment of both nuclides was observed at all the sites investigated in this study, suggesting that the soils had undergone little natural or anthropogenic disturbance for at least the last several decades. Apparent annual burial rates of ¹³⁷Cs (0.1–0.2 cm y^??1) were estimated to be about 1.3 times higher than those of ²¹⁰Pb at individual sites of different lithology, which suggests strong affinity of ²¹⁰Pb to soil organic matter. Variability of the vertical distribution profiles of these nuclides depends not only on “in situ” pedology but also on geographical and meteorological conditions, especially precipitation and wind direction.     

Characterization and correlation of Upper Jurassic (Oxfordian) bentonite deposits in the Paris Basin and the Subalpine Basin, France

Abstract Explosive volcanic activity is recorded in the Upper Jurassic of the Paris Basin and the Subalpine Basin of France by the identification of five bentonite horizons. These layers occur in Lower Oxfordian (cordatum ammonite zone) to Middle Oxfordian (plicatilis zone) clays and silty clays deposited in outer platform environments. In the Paris Basin, a thick bentonite (10–15 cm), identified in boreholes and in outcrop, is dominated by dioctahedral smectite (95%) with trace amounts of kaolinite, illite and chlorite. In contrast, five bentonites identified in the Subalpine Basin, where burial diagenesis and fluid circulation were more important, are composed of a mixture of kaolinite and regular or random illite/smectite mixed-layer clays in variable proportions, indicating a K-bentonite. In the Subalpine Basin, a 2–15 cm thick bentonite underlain by a layer affected by sulphate–carbonate mineralization can be correlated over 2000 km². Euhedral zircon, apatite and biotite crystals have been identified in all the bentonites. The geochemical composition of the bentonites in both basins is characterized by high concentrations of Hf, Nb, Pb, Ta, Th, Ti, U, Y, Zr and low concentrations of Cr, Cs and Rb. Biostratigraphical and geochemical data suggest that the thick bentonite in the Paris Basin correlates with the thickest bentonite in the Subalpine Basin, located 400 km to the south. These horizons indicate that significant explosive volcanic events occurred during the Middle Oxfordian and provide potential long-distance isochronous marker beds. Immobile element discrimination diagrams and rare-earth element characteristics indicate that the original ash compositions of the thickest bentonites correspond to a trachyandesitic source from a within-plate alkaline series that was probably related to North Atlantic rifting.     

137Cs reference site characteristics in Hong Kong — Some considerations

The distribution of ¹³⁷Cs is being assessed at input reference sites in Hong Kong. This work suggests that, in certain landscapes, difficulties in identifying potential reference sites and subsequently confirming site stability exert some constraints on ¹³⁷Cs measurement programmes. While the value of guidelines on site and sample selection has been reaffirmed, concern has emerged about the vertical distributions that may be taken to indicate reference site stability.The decline of ¹³⁷Cs concentrations down a reference soil profile are often reported to be exponential. Recently, a more complex profile with depleted ¹³⁷Cs totals at the soil surface has been reported and discussed. Thus there is no clear standard for a reference profile, though the profile has been the only empirical control on a reference site's suitability after selection.This study presents the depth distribution and spatial variation of ¹³⁷Cs areal activities at three reference sites in Hong Kong. The three sites have different spatial variability and different depth distributions, and serve to illustrate the difficulty of using vertical depth distributions as a confirmation of site stability. One possible independent check is the expected ¹³⁷Cs total from rainfall records; another is numerical modelling of the predicted profile given the physical and chemical controls on soil ¹³⁷Cs in reference site profiles.     

Chernobyl 137Cs redistribution in the small basin of the Lokna river,Central Russia

The redistribution of Chernobyl ¹³⁷Cs within a small drainage basin was studied in the Lokna river basin, Tula region, Central Russia. Sheet erosion on the cultivated part of basin is the main reason for ¹³⁷Cs horizontal migration. However there is no statistically significant ¹³⁷Cs redistribution within cultivated field because of relatively low erosion rates. The valley bottom is the main sink of ¹³⁷Cs, where 73–84% eroded soil is stored. The resulting ¹³⁷Cs level in the valley bottom is 1.5–2 times that of the initial ¹³⁷Cs fallout.     

Transport and sediment accumulation of210Pb and137Cs in two Southeast Alaskan fjords

Sediment profiles of²¹⁰Pb and¹³⁷Cs in cores collected at increasing distances from the heads of Smeaton Bay and Boca de Quadra fjords indicate that watersheds influence the inventories of radioisotopes present and that the steep topographies of the fjords enhance sediment redistribution. Episodic deposition of terrestrially derived sediment was responsible for roughly 50% of the¹³⁷Cs and 45% of the²¹⁰Pb inventories in shallower (less than 180 m) locations in Wilson and Bakewell arms of Smeaton Bay.²¹⁰Pb sedimentation rates at shallower sites when corrected for episodic deposition were less than sedimentation rates obtained in the deep basins of the fjords where sediment focusing and increased primary productivity in the overlying water column occur. Higher fluxes of dissolved Mn from surficial sediments and subsequent reoxidation in the overlying water may have enhanced scavenging of²¹⁰Pb in basin locations, resulting in higher inventories. Episodic events have occurred frequently in Smeaton Bay and Boca de Quadra suggesting that steady-state conditions with respect to sedimenting particles can be achieved only when averaged over long time periods approaching the time over which¹³⁷Cs and²¹⁰Pb are useful.     

东北四海龙湾玛珥湖沉积物纹层计年与137Cs、210Pb测年

对东北四海龙湾玛珥湖SHLF6孔纹层沉积物的¹³⁷Cs放射性测量表明:¹³⁷Cs比活度的最大值出现在55cm处,对应于1963年世界原子弹试爆高峰期。纹层计年表明0～6cm共有35个纹层层偶。从75cm到65cm,¹³⁷Cs比活度从256±009dpm/g急剧增加到1868±017dpm/g,可能65cm对应于1954年。通过测量²²⁶Ra子核²¹⁴Pb和²¹⁴Bi（能量为295keV,352keV和609keV）放射的光子数获得²²⁶Ra比活度数据,然后求得过剩²¹⁰Pb_{比活度（²¹⁰Pbuns）。²¹⁰Pbuns比活度随深度增加而呈指数衰减,其异常波动可能与人类活动以及沉积速率变化有关,例如55cm处²¹⁰Pb比活度较高,与¹³⁷Cs的峰值对应,这可能与1963年前后人工核实验的高峰有关,因为核试验不仅产生¹³⁷Cs,而且可以产生208Pb和²¹⁰Pb;45cm处²¹⁰Pb比活度较低,而²²⁶Ra较高,可能与人类活动加剧,导致沉积速率增加有关。根据²¹⁰PbunsCRS模式,SHLF6孔0～19cm的平均沉积速率为20mg/cm²·a,或约为011cm/a。²¹⁰Pb测年数据与¹³⁷Cs时标及纹层计年均有很好的一致性。四海龙湾玛珥湖发育的纹层为年纹层,可以建立高分辨率时间序列。}     

Determination of recent sedimentation rates in Lake Michigan using Pb-210 and Cs-137

This paper describes the use of ²¹⁰Pb and ¹³⁷Cs radioactivity measurements to determine the rates of sedimentation in the Great Lakes. Cores from eight locations in Lake Michigan were chosen for examination to cover as wide as possible a range of sedimentation rates and representative sedimentary environments. The surficial ²¹⁰Pb activity in the sediments varies between 7 and 23 pCi/g dry wt and its profile in each core shows the expected exponential decrease with depth consistent with the assumption of uniform sedimentation rate over the last hundred years and secular equilibrium between supported ²¹⁰Pb and ²²⁶Ra (0.5-1.0 pCi/g dry wt). Companion measurements of ¹³⁷Cs indicate that the coring technique satisfactorily recovered the uppermost levels of the deposit and that the mobility of both radionuclides within the sediment is probably small.Based on the limited number of cores analyzed to date, it appears that modern sedimentation rates are not very different from average rates for the last 7000 yr. The excess ²¹⁰Pb appears to originate primarily from atmospheric fallout, but a further inventory of the ²¹⁰Pb distribution over the lake bottom must be made to properly assess the significance of other sources. The spatial distributions of both ¹³⁷Cs and ²¹⁰Pb at certain stations suggest that the mode of transport of these radionuclides are comparable and involve attachment to settling particles. A mathematical model is developed which accounts for the observed limited mobility of both ²¹⁰Pb and ¹³⁷Cs in several of the cores in terms of post-depositional redistribution by physical or biological mixing processes.     

The pore water chemistry of 239,240Pu and 137Cs in sediments of Buzzards Bay,Massachusetts

The collection of large volumes of pore water (1–2 liters per 2 cm horizon of sediment) and low level radiochemical measurements of ^239,240Pu and ¹³⁷Cs have been combined to produce the first study of these fallout artificial radionuclides in marine pore waters. Profiles from box cores taken in June and September 1982 from Buzzards Bay, Mass., are reported along with profiles of many diagenetic constituents (i.e. SO₄^2?, alkalinity, Fe, Mn, DOC, and nutrients).The ^239,240Pu pore water profile is characterized by a subsurface maximum of about 0.28 dpm/100 kg lying between 3–11 cm. Overlying seawater, in contrast, has an activity of $\text{0.01 ± 0.02}$ dpm/100 kg. Below about 11 cm, the pore water ^239,240Pu distribution follows that of the solid phase which decreases rapidly with depth. The pore water profiles of ¹³⁷Cs are characterized by a broad and deeply penetrating maximum where activities of about 35–40 dpm/100 kg extend from 3 to 20 cm. Overlying seawater, in contrast, has an activity of 17–24 dpm/100 kg. The ¹³⁷Cs and ^239,240Pu pore water data show that there is preferential downward transport of ¹³⁷Cs and that ^239,240Pu does not have an active diagenetic chemistry and is not significantly mobile in these coastal sediments.     

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.     

Erosion rate in badlands of central Italy: estimation by radiocaesium isotope ratio from Chernobyl nuclear accident

The input of¹³⁷Cs into the troposphere from the Chernobyl nuclear accident made intriguing the use of fallout¹³⁷Cs as a tool for estimating the rate of soil erosion over Europe. The present paper reports on the adoption of¹³⁷Cs/¹³⁴Cs activity ratio to differentiate the vertical distribution of¹³⁷Cs prioir to and following the Chernobyl accident. The¹³⁷Cs/¹³⁴Cs activity ration in the radioactive clouds is required to calculate pre and post- 1986¹³⁷Cs amounts, considering that the whole¹³⁴Cs was actually derived from Chernobyl. By using this procedure, the erosion rates could be evaluated for the badland area, the Paglia River basin (central Italy), before and after the Chernobyl accident. Nine sites from two areas of this basin were sampled and analyzed. Erosion rates, ranging from 1.5 to 8.4 mm/a were measured, the values depending both on the basin lithology and site slope. These first results are consistent with those yielded by quantitative geomorphologic methods.     

近50年来抚仙湖重金属污染的沉积记录*

文章以抚仙湖污染严重的北部和基本未受人类活动影响的中部为研究对象,分别采集了沉积岩芯FB和FZ,通过对岩芯的¹³⁷ Cs测年和重金属元素(Cu,Ni,Ti,Cr,V,Pb,Cd和Zn)的含量分析,研究了湖泊重金属来源和污染历史,并利用地质累积指数法评价了湖泊重金属污染程度。结果表明:抚仙湖北部的平均沉积速率约为2.0~2.8mm/a;20世纪80年代以前,湖泊北部和中部的重金属元素(Cu,Ni,Ti,V,Pb,Cd,Zn)以自然来源为主;80年代以后,抚仙湖受到人类活动的影响,但湖泊中部Cu,Ni,Ti,V,Pb,Zn以及湖泊北部Cu,Ni,Ti,V仍以自然来源为主;湖泊北部Pb和Zn地质累积指数值小于1,属无污染到中度污染;北部Cd地质累积指数为3~4,达强度污染;中部Cd地质累积指数为2~3,属中强度污染;且Pb,Zn和Cd污染程度有加速增大的趋势。