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1.
At present, the prior-established threshold values are widely used to classify contaminated agricultural soils with heavy metals under the cultivation of a variety of crops, without considering the different sensitivity of plants to heavy metals. Evaluation of the characteristics of cadmium transfer from a polluted calcareous soil to cultivated wheat crop and assessment of the efficiency of using the threshold values to reflect the soil pollution risk by cadmium in Zanjan Zinc Town area at the northwest of Iran were the goals of this study. Totally, 65 topsoil (0–20 cm) and corresponding wheat samples of an agricultural region in the proximity of a metallurgical factory were collected and analyzed for cadmium concentration. The results revealed that industrial activities strongly control cadmium distribution in the studied soils. Relatively high bioavailable cadmium contents (mean 0.77 mg kg?1) were found in the soils, notwithstanding their alkalinity. It was observed that just 22.5% of the studied area around the Zinc Town is covered by polluted soils with the cadmium concentration exceeding the maximum permissible concentration of 5 mg kg?1, whereas cadmium concentration in wheat grains of 19 sampled plants is higher than the threshold value of 0.2 mg kg?1. Among these polluted plants, a total of eight samples were grown in areas classified as unpolluted soils with cadmium, based on the soil threshold value. It seems that this misclassification of polluted soils is mainly related to the crop sensitivity to heavy metals uptake from the soil which should be considered.  相似文献   

2.
The ability of light expanded clay aggregate to remove lead and cadmium from paint industry’s effluents was studied at different levels of adsorbent, contact time and pH in April 2008. For this purpose, lead and cadmium removal from paint industry effluents were studied in batch reactors. lead and cadmium measurements have been taken with non-flame atomic absorption techniques and test methods were adapted from 19th. Ed. of standard methods for the examination of water and wastewater. In this study, different amounts of Leca (1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 g/L) were investigated. The amount of adsorbed lead and cadmium exposure to Leca increased from 1.41 to 3 mg/g and 0.22 to 0.75 mg/g, respectively. The maximum removal efficiency for Pb was 93.75 % at pH = 7 and exposure to 10 g/L of Leca, while for cadmium, it was nearly 89.7 % at the same condition. In this study, adsorption process of lead and cadmium was fitted with Freundlich adsorption isotherm (R2 Pb = 0.97 and R2 Cd = 0.98). The sufficient contact time was deemed 1–2 h for lead and cadmium. According to the results, Leca is recommended as a low cost and available adsorbent to remove lead and cadmium from industrial wastewater.  相似文献   

3.
Vertical transport of selected polycyclic aromatic hydrocarbons (PAHs) in different particle-size fractions of sandy soils was investigated by simulation experiments in soil columns. Tested soil samples were fractionized into three particle-sizes including sand, coarse silt and fine silt (2,000–50, 50–20 and <20 μm). Rainfall simulations were conducted in artificially PAHs contaminated soil columns with 30 cm length and 5 cm diameter in 40 days. PAHs were extracted from soil samples and determined by high performance liquid chromatography (HPLC). Results showed that the residue level of PAHs in fine silt fraction reached 35.85 mg/kg, which was significantly higher than those in sand and coarse silt fraction (16.28 and 11.80 mg/kg, respectively), probably because PAHs in macroporous fractions were prone to volatilize or degrade compared with that in microporous fractions. Linear relationship between the residue levels of individual PAH (R PAHs) and the value of partition coefficient (log K oc) was regressed as R PAHs = 1.55 × log K oc − 5.86, R 2 = 0.91, n = 9. These results indicated that vertical transport of the mixed PAHs in soils were controlled both by the nature of PAHs (i.e. log K oc, molecular weight), soil particle size and soil organic contents, which could influence the transport of PAHs.  相似文献   

4.
Tubifex tubifex has been shown to survive in organic polluted environments, however, not much has been done on its inorganic pollution tolerance. Samples of T. tubifex and their respective sewage sludge were taken from Soche wastewater treatment plant in Blantyre City, Malawi during July 2007 to November 2008. The total number of sludge samples taken was fifty one which was made into seventeen composite samples. A total of seventeen T. Tubifex samples were also collected. The samples were analyzed for copper, lead, manganese, zinc and cadmium using standard methods from American Public Health Association and Association of Official Analytical Chemists. The concentrations of metals in sewage sludge and T. tubifex were on dry weight basis and the metals determined were acid extractable. In general, heavy metals concentration was lower in T. tubifex than in sewage sludge. The range of heavy metals concentrations were (in sludge and (T. tubifex)): zinc 275.3–361.5 mg/kg (45.0–82.2 mg/kg), manganese 293.7–230.1 mg/kg (1.21–3.69 mg/kg), copper 86.5–120.1 mg/kg (1.6–4.7 mg/kg), lead 11.2–22.4 mg/kg (Below detection limit–0.95 ) and cadmium 1.12–2.31 mg/kg (1.08–2.18 mg/kg). The results showed significant differences between the concentrations of manganese, copper, lead and zinc in sewage sludge and T. tubifex (p < 0.05). However there was no significant difference between the concentrations of cadmium in sewage sludge and T. tubifex (p > 0.05). T. tubifex did not show the ability to accumulate heavy metals (attributed to its high defecation and metabolic rate) except for cadmium hence cannot be used as a bioindicator for heavy metal pollution in sludge.  相似文献   

5.
Core sediments from two boreholes and groundwater from fifty four As-contaminated well waters were collected in the Chapai-Nawabganj area of northwestern Bangladesh for geochemical analysis. Groundwater arsenic concentrations in the uppermost aquifer (10 to 40 m of depth) range from 2.76?C315.15 mg/l (average 48.81 mg/l). Arsenic concentration in sediments ranges from 3.26?C10 mg/kg. Vertical distribution of arsenic in both groundwater and sediments shows that maximum As concentration (462 mg/l in groundwater and 10 mg/kg in sediments) occurs at a depth of 24 m. In January 2008, 2009 and 2010, maximum As concentration occurs at the same depth. Environmental scanning electron microscope (ESEM) with EDAX was used to investigate the presence of major and trace elements in the sediments. The dominant groundwater type is Ca-HCO3 with high concentrations of As and Fe, but with low levels of NO3 ? and SO3 ?2. Statistical analysis clearly shows that As is closely associated with Fe (R2 = 0.64) and Mn (R2 = 0.91) in sediments while As is not correlated with Fe and Mn in groundwater samples. Comparatively low Fe and Mn concentrations in some groundwater, suggest that probably siderite and/or rhodochrosite precipitated as secondary mineral on the surface of the sediment particles. The correlations along with results of sequential leaching experiments suggest that reductive dissolution of FeOOH and MnOOH mediated by anaerobic bacteria represents mechanism for releasing arsenic into the groundwater.  相似文献   

6.
This study reports on trace metal uptake by the grass species Melinis repens, growing in roadside soils and sediments in tropical northeastern Australia. Median total Cu, Pb, Ni and Zn concentrations were significantly (P < 0.05) higher in road edge soils (Cu = 61.1 mg/kg, Pb = 97.3 mg/kg, Ni = 28.6 mg/kg, Zn = 729 mg/kg) than in background soils collected away from roads (Cu = 5.8 mg/kg, Pb = 11.2 mg/kg, Ni = 3.7 mg/kg, Zn = 21 mg/kg). Significantly (P < 0.05) elevated Zn values were recorded in the stems of the M. repens specimens growing on roadside soils (231.6 mg/kg dry weight of tissue) compared with those of grasses growing on background soils (40.8 mg/kg dry weight of tissue). Moreover, median Cu, Ni and Zn values in the roots of roadside grasses (Cu = 29.1 mg/kg, Ni = 2.73 mg/kg, Zn = 169 mg/kg) were significantly (P < 0.05) higher than their respective levels in the roots of background M. repens samples (Cu = 5.98 mg/kg, Ni = 0.70 mg/kg, Zn = 22 mg/kg). A greenhouse experiment showed that Cu and Zn in road sediments are labile and are available for uptake by M. repens. The studied roadside soils and sediments were leached with a diethylenetriaminepentaacetic acid–CaCl2–triethanolamine–HCl extraction solution, which proved to be a rudimentary indicator of Zn availability and uptake to the root tissue of M. repens. The results demonstrate that trace metals in roadside grasses have the potential to be directed up the food-chain as grasses are consumed by herbivores. In addition, bioavailable metal contaminants hosted by road sediments have the capacity to impact on ecosystems downstream of roads because these sediments are mobilised by road runoff waters from road surfaces into adjoining catchments.  相似文献   

7.
Heavy metal concentrations in samples collected from the London 2012 Olympic Village were determined using a three-step sequential extraction and a rapid extraction method. Metal toxicity was measured by employing the Microtox? solid phase analysis. Both extraction methods produced comparable results (p?=?0.996), but the rapid method produced higher readings. A number of heavy metals were detected using the two extraction methods, including aluminum, arsenic, cadmium, chromium, copper, iron, nickel, lead and zinc; beryllium, molybdenum, niobium and titanium were also found in low concentration ranging between 0.16 and 27.10?mg/kg in the total acid digestion. The total metal levels in all the soil samples were within the UK Soil Guideline Value (SGV) except for lead which ranged between 62.9 and 776.2?mg/kg. The 30?min EC50 of different soil fractions was 2?C5.8?g/L. In the absence of any of heavy metals in the SGV, the Dutch Guideline values were referred. Mathematical models for a number of metals were generated based on the changes in EC50 values between each (F1, F2 and F3) soil fractions and the initial toxicity in the non-fractionated samples. The resulting models produced good R2 values (>96%) for predicting the change in toxicity of lead, cadmium, zinc and copper by measuring their changes in concentrations. These models could substantially reduce the time requires to determine the toxicity in the samples; they would be a useful tool in the clean up process where monitoring of metal toxicity is required.  相似文献   

8.
Soils (n=250) were collected from ten salt and brackish-water marshes of North Carolina and analyzed for organic matter content by loss on ignition (LOI) and Kjeldahl nitrogen (KN). Total organic carbon and total nitrogen were determined on the same samples using an elemental CHN analyzer. Regression analyses indicated that LOI and KN were excellent estimators of organic C (R2=0.990) and total N(R2=0.986), respectively, in low clay content (0–11%) marsh soils containing a wide range of soil organic C (0.1–28%) and total N (0–1.6%). A quadratic equation best described the relationship between organic C and organic matter (Organic C=0.40 [LOI] +0.0025 [LOI]2) while a linear model accurately described the relationship between total N and Kjeldahl N (Total N=1.048 [KN]?0.010). The proportion of organic C in organic matter (C/OM) increased with increasing soil organic matter content, probably as a result of aging. Young marshes, which are characterized by low soil organic content contain C/OM ratios similar to emergent vegetation (40–45%). In old organic soils (70–80% organic matter), C/OM increased to 57–60% due to accumulation of reduced organic materials.  相似文献   

9.
The ability of ion-exchange resin for ammonia removal from aqueous solution was studied. The results showed that Amberlite ion-exchange resin was effective in removing ammonia from aqueous solution. Factorial design and response surface methodology were applied to evaluate and optimize the effects of pH, resin dose, contact time, temperature and initial ammonia concentration. Low pH condition was preferred with the optimum pH found to be 6. High resin dose generated high removal rate and low exchange capacity. Results of factorial design and response surface methodology showed that temperature was not a significant parameter. The model prediction was in good agreement with observed data (R 2 = 0.957). The optimum Q e was 28.78 mg/g achieved at pH = 6 and initial TAN concentration of 3000 mg/L. The kinetics followed the pseudo-second-order kinetic model (R 2 = 0.999). Equilibrium data were fitted to Langmuir and Freundlich isotherm models with Langmuir model providing a slightly better predication (R 2 = 0.996). The resin was completely regenerated by 2 N H2SO4.  相似文献   

10.
An investigation was undertaken regarding the adsorption of different heavy metal ions from aqueous solutions using ??-diketone-functionalized styrene divinylbenzene resin under different experimental conditions such as initial concentration of metal ions, contact time, pH, and chelating capacity. The functionalization of resin was carried out by the condensation reaction of sodium salt of ??-diketones (pentane-1,3-dione) and chloromethylated styrene?Cdivinylbenzene resin in dichloromethane. Functionalized resin beads were characterized by Fourier transform infrared spectroscopy. The batch method was employed using different metal ions solution from 5 to 15?mg/L at different contact times. The adsorption kinetics was tested for the pseudo-first order, pseudo-second order reaction at different experimental conditions. The rate constant of adsorption kinetic models were also calculated and good correlation coefficient (R 2?>?0.9941) was obtained for pseudo-second order kinetic model. The maximum adsorption value obtain for lead (0.725728?mg/g), chromium (0.9199?mg/g), nickel (0.4974?mg/g), cobalt (0.6196?mg/g) and cadmium (0.6519?mg/g) at equilibrium condition, which shows that ??-diketone-functionalized styrene divinylbenzene resin is an effective adsorbent for toxic metal ions.  相似文献   

11.
Groups of embryonic grass shrimp,Palaemonetes pugio, were exposed to 0.1 and 0.3 mg/l cadmium at 30 ppt salinity and 25°C for the last 1, 4 or 8 days prior to hatching. Other groups of embryos were cultured in uncontaminated seawater. Prehatch exposure to cadmium was found to have no additive effect on the sensitivity of the larvae to cadmium exposure and salinity stress for 14 days after hatching. Only one group of larvae, exposed to 0.1 mg/l cadmium for 4 days before hatching, and transferred to 10 ppt salinity water containing 0.1 mg/l cadmium after hatching, showed a significant (X 2, P<0.05) decrease in survival, compared to control survival. No significant decreases in survival were observed for any larvae transferred to 15 and 30 ppt salinity at a pre- and posthatch cadmium concentration of 0.1 mg/l. At a pre- and posthatch cadmium concentration of 0.3 mg/l, significant decreases in survival were observed for all of the larvae transferred to 10 and 15 ppt salinity after hatching. Significant decreases in survival were observed for only 2 of the groups exposed before hatching and transferred to 30 ppt salinity and 0.3 mg/l cadmium after hatching.  相似文献   

12.
A pot culture experiment was conducted to study impact and interaction of multi-metals on growth, yield and metals uptake by spinach (variety All Green). Three levels of each chromium (0, 50 and 100 mg/kg), cadmium (0, 1 and 2 mg/kg) and zinc (0, 10 and 20 mg/kg) in combinations (total treatments 3 × 3 × 3 = 27) were applied in a Vertisol (5 kg). The results showed that increasing the concentration of chromium, cadmium and zinc in soil enhanced the respective metal concentrations in spinach root and shoot. When cadmium at 2 mg/kg along with chromium at 100 mg/kg soil was applied, chromium concentration and uptake were decreased in root and shoot. Meanwhile, zinc application had no significant effect on chromium uptake and concentration in spinach biomass. From the results, it was concluded that cadmium at higher dose had an antagonistic effect over chromium. On the other hand, in chromium, cadmium and zinc combinations particularly at their higher levels, a competition among each other was found. Therefore, the findings could be used as guidelines for controlling and management of heavy metals pollution in farmland.  相似文献   

13.
Improvement of cadmium ion electrochemical removal from dilute aqueous solutions in a spouted bed reactor was investigated. Enlargement of cathode surface area from 1,000 to 1,500 cm2 resulted in a decrease of nearly 30 % in both of the process time and the specific energy consumption. Application of a three-stage electrolysis process for a solution containing initial concentration of 270 ppm cadmium ion, resulted in the removal of 99.9 % cadmium ion in 135 min with the specific energy consumption of 2.29 kWh/kg, 23 % less than the value of a single-stage process. For a solution with cadmium ion initial concentration of 180 ppm, 99.9 % of cadmium ion was removed in 135.5 min by application of a two-stage electrolysis process, while the specific energy consumption was 2.82 kWh/kg, 30 % less than that of a single-stage process. For a solution with cadmium ion initial concentration of 90 ppm, 99.5 % of cadmium ion was removed in 100.2 min with the specific energy consumption of 3.78 kWh/kg in a single-stage electrolysis process.  相似文献   

14.
《Applied Geochemistry》2001,16(11-12):1369-1375
The heavy metal contamination of soils and waters by metalliferous mining activities in an area of Korea was studied. In the study area of the Imcheon Au–Ag mine, soils and waters were sampled and analyzed using AAS for Cd, Cu, Pb and Zn. Analysis of HCO3−, F−, NO3− and SO42− in water samples was also undertaken by ion chromatography. Elevated concentrations of the metals were found in tailings. The maximum contents in the tailings were 9.4, 229, 6160 and 1640 mg/kg extracted by aqua regia and 1.35, 26.4, 70.3 and 410 mg/kg extracted by 0.1 N HCl solution for Cd, Cu, Pb and Zn, respectively. These metals are continuously dispersed downstream and downslope from the tailings by clastic movement through wind and water. Because of the existence of sulfides in the tailings, a water sample taken on the tailings site was very acidic with a pH of 2.2, with high total dissolved solids (TDS) of 1845 mg/l and electric conductivity (EC) of 3820 μS/cm. This sample also contained up to 0.27, 1.90, 2.80, 53.4, 4,700 mg/l of Cd, Cu, Pb, Zn and SO42−, respectively. TDS, EC and concentrations of metals in waters decreased with distance from the tailings. The total amount of pulverized limestone needed for neutralizing the acid tailings was estimated to be 46 metric tons, assuming its volume of 45,000 m3 and its bulk density of 1855 kg/m3.  相似文献   

15.
Soil samples from 0 to 100 cm depth were collected in four sampling sites (Sites A, B, C and D) along a 250-m length of sampling zone from the Yellow River channel to a tidal creek in a seasonal flooding wetland of the Yellow River Delta of China in fall of 2007 and spring of 2008 to investigate spatial and seasonal distribution patterns of total phosphorous (TP) and available phosphorus (AP) and their influencing factors. Our results showed that TP contents in spring and AP contents in both seasons in surface soils increased with increasing distances away from the Yellow River channel. TP contents in surface soils (0–10 cm) followed the order Site A (698.6 mg/kg) > Site B (688.0 mg/kg) > Site C (638.8 mg/kg) > Site D (599.2 mg/kg) in fall, while Site C (699.6 mg/kg) > Site D (651.7 mg/kg) > Site B (593.6 mg/kg) > Site A (577.5 mg/kg) in spring. Generally, lower TP content (630.6 mg/kg) and higher AP level (6.2 mg/kg) in surface soils were observed in spring compared to fall (656.2 mg/kg for TP and 5.2 mg/kg for AP). Both TP and AP exhibited similar profile distribution patterns and decreased with depth along soil profiles with one or two accumulation peaks at the depth of 40–80 cm. Although the mean TP content in soil profiles was slightly higher in spring (635.7 mg/kg) than that in fall (628.0 mg/kg), the mean TP stock was obviously lower in spring (959.9 g/m2) with an obvious accumulation at the 60–80 cm soil depth compared to fall (1124.6 g/m2). Topsoil concentration factors also indicated that TP and AP had shallower distribution in soil profiles. Correlation analysis showed that AP had significant and positive correlation with these soil properties such as soil organic matter, salinity, total nitrogen and Al (p < 0.01), but TP was just significantly correlated with TN and Al (p < 0.05).  相似文献   

16.
江苏宜溧富硒稻米产区地质地球化学背景   总被引：4，自引：0，他引：4       下载免费PDF全文
江苏宜溧地区分布有400 km2多的富硒土壤,并产出天然富硒稻米。通过系统分析研究宜溧富硒稻米产地的稻米、土壤、岩石、水样的Se等元素地球化学数据,探讨了控制宜溧地区富硒稻米产出的主要地质环境及地球化学背景因素,总结了Se等元素在米-土-岩之间的分布迁移特征。结果显示:(1)宜溧地区产出的富硒稻米主要受富硒耕地控制,稻米Se与耕地土壤Se、Corg.之间存在显著正相关性,米Se与土Se的相关系数R=0.81,土壤Se≥0.5 mg/kg的耕地中富硒稻米检出率为100%;(2)二叠系煤系地层中的杂色泥质粉砂岩、页岩是主要富硒原岩,其平均Se含量达到17.22 mg/kg,比当地土壤中Se高出5倍以上。富硒原岩沉积厚度越大,其上覆土壤的Se含量越高;(3)上述富硒岩层中夹杂一层几到几十厘米厚的铁锰结核透镜状沉积物,富集Fe、Mn、Cd、S、P等,其风化形成土壤可能富集Cd,但富硒稻米中未检测到Cd超标;(4)耕地土壤中有效Se小于0.02 mg/kg,有效Se占土壤Se的比例为0.16%~2%。富硒耕地土壤总体偏酸性,其p H一般介于4.6~6.5,富硒原岩更偏酸性,其p H一般介于4.2~5.5;(5)Se从源头向耕地迁移也是一个不断均匀化的过程,地势、气候条件、断层等对富硒耕地的分布有影响,山间盆地、沟谷、山前平原是形成天然富硒耕地的主要场所,特定断层可成为天然富硒耕地的边界。  相似文献   

17.
Sediments from unpolluted and highly polluted lakes in northern Ontario have been fractionated into acid volatile sulfide, HCl-soluble sulfur, elemental sulfur, pyrite sulfur, ester sulfate and carbon-bonded sulfur and the isotopic composition of each fraction determined. In general, reduced inorganic S constitutes 25–50% of the total S in the polluted surficial sediments, but is <20% in the unpolluted samples, with pyrite formation being a minor process of S diagenesis in lake sediment ecosystems. Organic S in the form of ester sulfate and carbon-bonded S predominates and both the C/S ratios and the isotopic data suggest that, in unpolluted lakes, plant detritus can be a major contributor of organic-S to the sediments. The depth profiles observed suggest that the more labile ester sulfate is diagenetically converted to the carbon-bonded form. For the polluted sediments from the Sudbury basin, the isotopic data suggest that (a) the elemental S is derived from the oxidation of acid volatile sulfide in the aerobic surficial sediments, and (b) the isotopically light reduced S species are incorporated into the organic material. S diagenesis in lake sediments generally results in the release of 34S to the overlying water. The suggestion is made that sulfate concentrations over 5 mg/1 accompanied by an enrichment of surficial sediments with isotopically different S may signal significant inputs of pollutant S into the lake and its basin.  相似文献   

18.
Excessive soil copper (Cu) availability leads to plant growth retardation and leaf chlorosis, and the contamination of Cu in the food chain would be detrimental to human and animal health. The most important path for Cu accumulation in plants is uptake from soils. It is therefore important to understand the availability of soil Cu and its controlling factors to modify Cu availability and prevent excessive Cu from entering the food chain. The present study proposed a general regression neural network (GRNN) to simulate the availability index of soil Cu (available heavy mental concentrations/total heavy metal concentrations), based on the influencing factors of total Cu concentration, pH, organic matter (OM), available phosphorus (AP), and readily available potassium (RAK). Results showed that total Cu concentration, combined with OM and AP, achieved the lowest RMSE value (0.0524) for the modeled value of the availability index of soil Cu. The simulated results by GRNN and the ground truth values had better agreement (R 2 = 0.7760) than that by a linear model (R 2 = 0.6464) for 23 test samples. Moreover, GRNN obtained lower averaged relative errors than linear model. This demonstrated that GRNN could be used to simulate the availability index of soil heavy metals and gained better results than linear model.  相似文献   

19.
《Geochimica et cosmochimica acta》1999,63(23-24):4005-4012
Previous studies have shown that 187Os/188Os in seawater has become increasingly radiogenic over the last 40 Ma in a manner analogous to strontium. This rapid rise in the marine 187Os/188Os over the last 17 Ma has been attributed to an increase in the bulk silicate weathering rates resulting from the rise of the Himalayas and/or selective weathering and erosion of highly radiogenic organic rich ancient sediments. The key test of this hypothesis is the 187Os/188Os and the total osmium concentration of the Himalayan rivers. We report the concentration and isotopic composition of osmium in the Ganges, the Brahmaputra, and the Indus rivers. The 187Os/188Os of the Ganges close to its source (at Kaudiyal, 30°05′N, 78°50′E) is 2.65 and [Os] = 45 fM/kg. A second sample of the lower reaches of the Ganges at Patna (25°30′N, 85°10′E) gives 187Os/188Os =1.59 and [Os] = 171 fM/kg. The 187Os/188Os of the Brahmaputra at Guwahati (26°10′N, 91°58′E) is 1.07 and [Os] = 52 fM/kg. A sample of the Indus (Besham, 34°55′N, 72°51′E) has a 187Os/188Os of 1.2 and [Os] = 59 fM/kg. We infer that the Himalayas do not provide either a high flow of osmium or a highly radiogenic osmium component to the oceans. The overall trend for osmium and strontium could be explained by a regularly increasing input of global continental weathering sources but the Himalayas themselves appear not to be the dominant source.  相似文献   

20.
富硒土地资源研究进展与评价方法   总被引：13，自引：0，他引：13  
周国华 《岩矿测试》2020,39(3):319-336
硒是重要的生命必需元素,开发富硒农产品是提升我国人体硒摄入水平的安全有效途径,富硒土地资源评价与利用规划是土地质量地球化学调查成果服务于特色农产品发展与脱贫攻坚的重要切入点。本文评述了近年来在土壤和作物硒含量、土壤硒成因来源、土壤硒赋存形态及其生物有效性影响因素、土壤-作物系统硒吸收运移、硒与重金属镉等元素之间的相互作用等调查研究成果。针对我国土壤硒背景值约0.20mg/kg,远低于世界土壤背景值0.40mg/kg,整体上处于低硒水平的实际情况,认为采用0.40mg/kg Se作为富硒土壤标准具有较强的科学依据;多数情况下土壤硒主要来源于成土地质背景,部分地区与人为活动密切有关;富硒土壤可分为地质高背景、次生富集作用、人为输入及其多种作用的叠加成因,元素地球化学性质决定了硒与镉等重金属元素共生的普遍性;土壤硒成因来源以及pH、Eh、有机质、铁铝氧化物等土壤理化条件决定了硒和重金属赋存形态与生物有效性,进而影响到富硒土地的可利用性,成为制定富硒土壤地方标准的理论基础与考虑因素;不同作物种类对硒吸收富集能力不同,筛选适应当地农田生态环境、富硒低镉的农作物具有实际意义;现有的部分富硒农产品标准未充分考虑人体补硒目的,并存在标准间协调性差等问题,急需加强富硒农产品标准的制定。本文提出,富硒土地资源评价不仅需要考虑土壤硒和重金属含量,而且需综合土壤硒成因来源及其生物有效性、土壤-作物系统硒迁移累积、硒与重金属镉等元素之间的相互作用机制,以及当地气候、土壤和景观条件下作物种植的适宜性,依据富硒土地资源可利用性进行分类分区、科学规划和合理种植管理。同时建议,为满足富硒土地资源调查评价与可利用性分析、富硒农产品健康效应研究的需要,需要加强土壤和作物硒含量及其形态的提取分离与分析测试方法技术研究与应用。  相似文献   

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