Contamination history of suspended river sediments accumulated in oxbow lakes over the last 25 years

Background, aims, and scope  Embankment of meandering river systems in many industrial areas results in the formation of artificial oxbow lakes that may act as perennial or intermittent traps for river sediments. Their deposits can be dated using a combination of historical and stratigraphic data, providing a good means to study historical records of contamination transported by rivers. Contamination history over the last few decades is of special significance for Central and Eastern Europe as it can reflect high pollutant levels in the second half of the twentieth century and the subsequent improvement after the fall of the Iron Curtain. The purpose of this study was to investigate recent sediments of an oxbow lake of the Morava River, Czech Republic, their stratigraphic records, sediment architecture, and history of contamination. Materials and methods  Seven ground-penetrating radar (GPR) profiles and three sediment cores up to 4 m deep were studied. The stratigraphy of the cores was inferred from visible-light spectrophotometry, X-ray radiography, grain size analysis, and semiquantitative modal analysis of sandy fractions. The sediments were dated using the ¹³⁷Cs mass activity and combinations of stratigraphic and historical data. The cores were sampled for concentrations of heavy metals and persistent organic pollutants. Wet sampled, lyophilized, and sieved sediments were extracted and analyzed for heavy metals by inductively coupled plasma mass spectrometry (ICP-MS) of aqua regia leachate and for persistent organic pollutants by gas chromatography (GC-ECD and GC-MS). Results  Three distinct sedimentary sequences (S1, S2, and S3) were identified. The basal sequence S1 represents river channel sediments deposited before the formation of the oxbow lake, most likely before the 1930s. The boundary between the S1 and S2 sequence correlates with the level of sediment dredging from 1981 evidenced from historical data. The overlying sequences S2 and S3 represent a postdredging sediment wedge, which progrades into the lake. ¹³⁷Cs dating revealed a distinct Chernobyl 1986 peak at ∼150 cm depth inferring sedimentation rates up to 7.7 cm/year. Sediment contamination abruptly increased from the pre-1930s deposits to the post-1981 deposits. The concentration levels increased two to five times for Pb, As, Zn, and Cu, about 10 to 15 times for Cr, Sb, and Hg, up to 34 times for Cd, and 25 to 67 times for DDTs, PCBs, and PAHs. The concentrations of most contaminants remained approximately constant until the late 1980s when they started to decrease slowly. The decreasing trends were most prominent for heavy metals and anthracene, less prominent for DDTs, and almost absent for PCBs and most PAHs. Discussion  Different temporal and spatial patterns for various contaminants make it possible to distinguish between anthropogenic point sources from local industry (anthracene, Cr, Cd), possible diffuse sources (most PAHs), and geological background (V, Co, Ni, and Mo). The observed recent trends in heavy metal and persistent organic pollutant contamination are generally consistent with data from other Central European rivers. The roughly balanced contamination levels in sediments from the lake and the adjacent river channel suggest that the oxbow lake deposits reflect immediate levels of the contamination bound to suspended particulate matter passing through the river. Conclusions  The investigated oxbow lake accumulated suspended sediment from Morava River, developing a thick sedimentary body. The sediments offer a good time framework to study historical contamination of the river on a decade time scale. Continuous contamination trends can be traced back to the early 1980s. The results show that stratigraphic analysis of cores has a good potential for identification of uninterrupted historical trends and unconformities, e.g., due to dredging. Recommendations and perspectives  Oxbow lakes may provide an alternative to floodplains and reservoir deposits when studying river contamination history. High sedimentation rates of up to 7.7 cm/year offer a very good stratigraphic resolution, making it possible to study contamination patterns on annual or even seasonal time scales. On the other hand, oxbow lakes may represent long-term contamination stores, which are unlikely to be redistributed by river erosion and, hence, may possess significant environmental risks for the farther future.     

Nitrogen retention and plant uptake on a highly weathered central Amazonian Ferralsol amended with compost and charcoal

Leaching losses of N are a major limitation of crop production on permeable soils and under heavy rainfalls as in the humid tropics. We established a field trial in the central Amazon (near Manaus, Brazil) in order to study the influence of charcoal and compost on the retention of N. Fifteen months after organic‐matter admixing (0–0.1 m soil depth), we added ¹⁵N‐labeled (NH₄)₂SO₄ (27.5 kg N ha^–1 at 10 atom% excess). The tracer was measured in top soil (0–0.1 m) and plant samples taken at two successive sorghum (Sorghum bicolor L. Moench) harvests. The N recovery in biomass was significantly higher when the soil contained compost (14.7% of applied N) in comparison to only mineral‐fertilized plots (5.7%) due to significantly higher crop production during the first growth period. After the second harvest, the retention in soil was significantly higher in the charcoal‐amended plots (15.6%) in comparison to only mineral‐fertilized plots (9.7%) due to higher retention in soil. The total N recovery in soil, crop residues, and grains was significantly (p < 0.05) higher on compost (16.5%), charcoal (18.1%), and charcoal‐plus‐compost treatments (17.4%) in comparison to only mineral‐fertilized plots (10.9%). Organic amendments increased the retention of applied fertilizer N. One process in this retention was found to be the recycling of N taken up by the crop. The relevance of immobilization, reduced N leaching, and gaseous losses as well as other potential processes for increasing N retention should be unraveled in future studies.     

Trends in grain yields and soil organic C in a long‐term fertilization experiment in the China Loess Plateau

Changes in grain yields and soil organic carbon (SOC) from a 26 y dryland fertilization trial in Pingliang, Gansu, China, were recorded. Cumulative C inputs from straw and root and manure for fertilizer treatments were estimated. Mean wheat (Triticum aestivum L.) yields for the 18 y ranged from 1.72 t ha^–1 for the unfertilized plots (CK) to 4.65 t ha^–1 for the plots that received manure (M) annually with inorganic N and P fertilizers (MNP). Corn (Zea mays L.) yields for the 6 y averaged 2.43 and 5.35 t ha^–1 in the same treatments. Yields declined with year except in the CK for wheat. Wheat yields for N only declined with time by 117.8 kg ha^–1 y^–1 that was the highest decrease among all treatments, and that for NP declined by 84.7 kg ha^–1 y^–1, similar to the declines of 77.4 kg ha^–1 y^–1 for the treatment receiving straw and N annually and P every second year (SNP). Likewise, the corn yields declined highly for all treatments, and the declined amounts ranged from 108 to 258 kg ha^–1 y^–1 which was much higher than in wheat. These declined yields were mostly linked to both gradual dry weather and nutrients depletion of the soil. The N only resulted in both P and K deficiency in the soil, and soil N and K negative balances in the NP and MNP were obvious. Soil organic carbon (SOC) in the 0–20 cm soil layer increased with time except in the CK and N treatments, in which SOC remained almost stable. In the MNP and M treatments, 24.7% and 24.0% of the amount of cumulative C input from organic sources remained in the soil as SOC, but 13.7% of the C input from straw and root in the SNP, suggesting manure is more effective in building soil C than straw. Across the 26 y cropping and fertilization, annual soil‐C sequestration rates ranged from 0.014 t C ha^–1 y^–1 for the CK to 0.372 t C ha^–1 y^–1 for the MNP. We found a strong linear relationship (R² = 0.74, p = 0.025) between SOC sequestration and cumulative C input, with C conversion–to–SOC rate of 16.9%, suggesting these dryland soils have not reached an upper limit of C sequestration.     

An integrative approach of organic matter stabilization in temperate soils: Linking chemistry,physics, and biology

With this topical issue, we present the work of the Priority Program 1090 of the German Research Foundation (“Deutsche Forschungsgemeinschaft DFG”): “Soils as a source and sink for CO₂ – mechanisms and regulation of organic matter stabilisation in soils”. This introduction gives an overview on the sites investigated and the major research approaches, including a glossary of major terms used in the field of soil organic matter research. We point out the advantages of integration of data from a broad field of different soil‐science disciplines and the progress achieved by application and combination of new analytical methods describing the quality and turnover of soil organic matter.     

Improved RP‐HPLC and anion‐exchange chromatography methods for the determination of amino acids and carbohydrates in soil solutions

In spite of their low concentrations in soil solutions, low–molecular weight organic substances (LMWOS) such as amino acids, sugars, and uronic acids play a major role in the cycles of C and N in soil. With respect to their low concentrations and to possible matrix interferences, their analysis in soil leachates is a challenging task. We established two HPLC (high‐performance liquid chromatography) methods for the parallel determination of amino acids and carbohydrates in soil leachates. The pre‐column derivatization of amino acids with an o‐phthaldialdehyde (OPA) mercaptoethanol solution yields quantitation limits between 0.03 and 0.44 µmol L^–1 and S_D values of <8.3% (n = 9). High‐performance anion‐exchange chromatography (HPAEC) on a Dionex CarboPac PA 20 column with a NaOH acetate gradient combined with pulsed amperometric detection (PAD) was used for the determination of carbohydrates. The calibration curves obtained for 11 carbohydrates showed excellent linearity over the concentration range from 0.02 to 50.0 mg L^–1. Recovery studies revealed good results for all analytes (89%–108%). Interferences from Hg(II) salts and chloroform used for stabilization of the leachates did not occur with both chromatographic methods. The optimized method was successfully used for quantitative determinations of amino acids and carbohydrates in soil leachates.     

添加活性炭对土壤有效磷测定的影响研究

针对NY/T 148-1990测定方法中,加活性炭目的是降低由于浸出土壤有机质所产生的颜色对有效磷测定结果的影响,但是却限制了土壤有效磷的批量测定,为此进行了不加活性炭条件下测定土壤有效磷的改进试验。试验结果表明,不加活性炭条件下,浸出土壤有机质所产生的颜色对土壤有效磷测定结果在测定误差范围内可以忽略不计;两种有效磷测定方法的平均值均在误差范围之内,但改进方法所测结果更接近于NY/T 148-1990标准值,测值间离散度低,稳定性强,且测定速度快、结果准确度及精密度高、成本低。     

不同有机肥配比对蔬菜产量和品质及土壤肥力的影响

试验选择了5种有机肥料,采用6种配比在生菜和青花菜上进行了试验。研究表明,鸡粪、猪粪、牛粪按1∶1∶3或按1∶1∶1配比,青花菜的产量显著高于鸡粪、猪粪、牛粪、草炭为1∶1∶1∶1的配比。鸡粪、猪粪、牛粪按1∶3∶1的配比能明显提高青花菜的Vc和可溶性糖含量。鸡粪、猪粪、牛粪、草炭、玉米秸秆按1∶1∶1∶1配比能明显提高青花菜的粗蛋白和Vc含量。     

Soil chemical properties and microbial biomass after 16 years of no-tillage farming on the Loess Plateau, China

Data from a 16-year field experiment conducted in Shanxi, on the Chinese Loess Plateau, were used to compare the long-term effects of no-tillage with straw cover (NTSC) and traditional tillage with straw removal (TTSR) in a winter wheat (Triticum aestivum L.) monoculture. Long-term no-tillage with straw cover increased SOM by 21.7% and TN by 51.0% at 0–10 cm depth and available P by 97.3% at 0–5 cm depth compared to traditional tillage. Soil microbial biomass C and N increased by 135.3% and 104.4% with NTSC compared to TTSR for 0–10 cm depth, respectively. Under NTSC, the metabolic quotient (CO₂ evolved per unit of MBC) decreased by 45.1% on average in the top 10 cm soil layer, which suggests that TTSR produced a microbial pool that was more metabolically active than under NTSC. Consequently, winter wheat yield was about 15.5% higher under NTSC than under TTSR. The data collected from our 16-year experiment show that NTSC is a more sustainable farming system which can improve soil chemical properties, microbial biomass and activity, and thus increase crop yield in the rainfed dryland farming areas of northern China. The soil processes responsible for the improved yields and soil quality, in particular soil organic matter, require further research.     

Response of an agricultural soil to pentachlorophenol (PCP) contamination and the addition of compost or dissolved organic matter

The response of a fresh, agricultural soil when contaminated with pentachlorophenol (PCP) and supplemented with compost (C) or dissolved organic matter (DOM) was studied in the laboratory. The concentration of PCP and the changes in various functionally related properties (i.e. microbial biomass, basal respiration, soil hydrolase and oxidoreductase activity) were measured over 150 d. Variations in the main physical and chemical properties of the soils were also monitored. Two different doses of compost (C1 = 0.27% and C2 = 0.83%, corresponding to 10 and 30 t ha⁻¹, respectively) or DOM (D1 = 0.07% and D2 = 0.2%) equivalent to the carbon content of the two compost doses C1 and C2 were used and the following five systems were investigated: soil (S), soil–compost (S-C1 and S-C2) and soil–DOM (S-D1 and S-D2). PCP concentrations declined progressively and significantly with time. This effect was most pronounced for the soils amended with the lower compost dose C1 (S-C1) and with the two DOM (S-D1 and S-D2) amounts. Significantly reduced amounts of PCP were extracted after its 500-d residence in the various systems. Higher amounts of the residual PCP were extracted from the humic acids (HA), fulvic acids (FA) and humin–mineral (HU) fractions of the 500 d aged samples than from the same unfractionated samples, indicating that the residual PCP preferentially accumulated in the organic fractions of soil. The soil showed an endogenous microbial activity as indicated by basal respiration, microbial biomass and all the enzymatic activities tested (dehydrogenase, glucosidase, phosphatase, arylsulphatase and urease). Addition of the PCP severely depressed some of the tested biochemical properties suggesting an inhibitory effect on microbial activity. Conversely, higher basal respiration, and similar β-glucosidase and phosphatase activities were measured in comparison with the controls. No significant effects were observed following the addition of two doses of the compost or the DOM. Fungal colonies belonging to the taxonomic group of Ascomycetes and identified as Byssochlamys fulva developed with time in all the PCP-contaminated samples. Growth of B. fulva in vitro in the presence of PCP showed that the isolate was tolerant to 12.5 and 25 mg l⁻¹ PCP and degraded 20% of its initial concentration in 8 d. Overall, the results indicate that many complex processes occurred in the contaminated soil and combinations of these determined the response to PCP contamination. The sorption of PCP to the soil matrix (which increased with time) and its degradation/transformation by indigenous soil microbial activity were likely involved. Both the processes appeared to be favoured by the presence of dissolved organic matter.