Characteristics of soil organic matter (SOM) extracted using base with subsequent pH lowering and sequential pH extraction

Humic substances from eight soils of varying properties were extracted by two different methods: (1) the traditional NaOH-extraction with subsequent acidification to different pH (approximately 1 to approximately 12) and sequential extractions using 0.01 M NaNO(3) at incremental pH (approximately 1 to approximately 11). Cumulative organic matter (OM) in the sequential extractions showed properties that were consistent with NaOH-extracted OM. The release of Al and Fe in the sequential extractions was closely related with the release of organic carbon (OC). The ratio of OC associated with humic acid (HA) and fulvic acid (FA) (the HA:FA ratio) varied widely among the soils indicating heterogeneity in their OM composition. However, a significant correlation between this HA:FA ratio and the NaOH extractable %OC content of the soils is indicative of the possible relationship between them. Between pH 5 and 7, which is a typical soil solution pH, a significant amount of HA-associated OC was soluble. In modeling metal speciation in soil solutions, it has been assumed that all dissolved organic carbon (DOC) that is active toward metal binding is associated with FA. The results of this study indicate that the validity of these assumptions based on model sensitivity alone is questionable.     

Enhancement of arsenic mobility by indigenous bacteria from mine tailings as response to organic supply

Arsenic leaching by indigenous bacteria in abandoned Au-Ag mine tailings which contained approximately 3200 mg/kg of As was investigated after supply of various organic substrates. Sequential extraction analysis designed to determine the mode of As occurrence in the tailings revealed that most As (90%) was closely associated with the Fe fraction. When glucose was supplied as a C source, indigenous bacteria significantly enhanced the extent of As release from the tailings into solution under both aerobic and anaerobic conditions. Anaerobic indigenous bacteria leached more amount of As from the tailings than aerobes. Highly positive correlation between the extracted amounts of As and Fe implied that microbial dissolution of Fe(III)-oxides, whether it was ligand- and proton-promoted dissolution or reductive dissolution, might be dominantly responsible for the As release. Bacterial strains which were resistant to up to 100 mM As(V) was aerobically isolated from the tailings. One of the isolates appeared to reduce some aqueous As(V) to likely As(III) in a batch type experiment, which indicated that indigenous bacteria can mediate the electrochemical speciation and thus the mobility of As in the tailings. The results suggest that indigenous bacteria in As-contaminated tailings can increase As mobility from the solid media when microbially available organic substrates are supplied, and thus enhance the risk of As dispersion to nearby soil, sediment and groundwater.     

鄱阳湖沙山植物叶片与土壤C∶N、C∶P沿沙化梯度分布特征

在鄱阳湖多宝沙山沿沙化梯度测定了17种常见植物叶片及土壤有机碳(C)、全氮(N)、全磷(P)含量,以阐明沙山常见植物种与土壤C〖DK〗∶N、C〖DK〗∶P分布特征及对沙化的响应,为沙山植被恢复提供基础数据。结果表明：（1）植物叶片C〖DK〗∶N、C〖DK〗∶P分布范围为185～1273、1698～5071,平均值分别为431、3418;土壤0～10、10～30、30～50 cm层C〖DK〗∶N变化范围分别为98～463、24～465和37～450; 相应土层C〖DK〗∶P范围分别为198～759、30～905和47～765。（2）植物C〖DK〗∶N、C〖DK〗∶P对沙化的响应模式一致,均表现出在重度沙化区数值最小;土壤C〖DK〗∶N随沙化程度增加表现出降低趋势,而C〖DK〗∶P则表现出增加趋势,二者对沙化的响应不一致。（3）植物C〖DK〗∶N、C〖DK〗∶P变化主要取决于叶片的N、P含量;土壤C〖DK〗∶N的变化受控于土壤N含量;C〖DK〗∶P变化则决定于土壤有机C含量     

Sediment accumulation rate and radiological characterisation of the sediment of Palmones River estuary (southern of Spain)

Chemical analyses and radioecological methods were combined in order to estimate the sediment accumulation rate in the upper 20 cm depth of the Palmones River estuary. Organic matter, total carbon, C:N and (137)Cs vertical profiles showed changes at 13 cm depth. These changes could be associated with the decrease in river input since 1987 when a dam situated in the upper part of the estuary started to store water. Using 1987 as reference to date the sediment, accumulation rate was 1.2 cm yr(-1). As alternative method, two layer model of (210)Pb(xs) vertical distribution showed a sedimentation rate of 0.7 cm yr(-1) with a surface mixing layer of 7 cm thickness. The high ammonium, potassium and sodium content in pore water and the strong correlation between (137)Cs activities and organic matter in dry sediment suggests that (137)Cs (the only anthropogenic product detected) is mainly accumulated in the estuary associated with the particulate organic material from the catchment area.     

巢湖及其入湖河流（南淝河）沉积物磷形态与吸附行为的垂直变化

沉积物磷释放可明显促进水体富营养化,但其关键组分与调控因素尚待深入研究。系统分析了巢湖及其入湖河流（南淝河）沉积物有机质(OM)、不同形态磷含量、磷吸附参数的垂直分布特征。结果表明：铁结合态磷(Fe(OOH)~P)与钙结合态磷(CaCO3~P)为沉积物磷的主要存在形态,且均与磷平衡浓度（EPC0）显著正相关。与巢湖相比,南淝河具有明显较高的沉积物最大磷吸附量（Qmax）,而由此增强的磷缓冲能力可被较高的Fe(OOH)~P含量所抵消,从而表现出较强的磷释放潜力（高EPC0值）。有机质能以线性方式增加Fe(OOH)~P、CaCO3~P与Qmax,并据此调节EPC0。南淝河沉积物亚表层（10～15 cm）显示EPC0的最小值,从而具有相对较小的磷释放风险     

Basic characterization of Norwegian NOM samples — Similarities and differences

NOM (natural organic matter) samples, isolated by reverse osmosis (RO), and nine NOM samples, concentrated by low-pressure, low-temperature evaporation (EVA) from various origin in Norway, were characterized by different methods. The methods included elemental content of the freeze-dried samples (C, H, N, and O), elemental content of the redissolved samples (DOC, Na, Ca, Cu, Fe, and Mn), specific spectral absorbance at λ = 254 nm (A(254 nm)/DOC) and at λ = 436 nm (A(436 nm)/DOC), UV/Vis-spectra, specific fluorescence (excitation and emission spectra), proton capacity, Cu-complexation capacity, and content of hydrolysable amino acids and carbohydrates. In addition, chromatographic characterization by gel chromatography and reversed-phase chromatography was done. Studies on adsorption and flocculation abilities and the formation of trihalomethanes (THM) and organic halogens adsorbable on activated carbon (AOX) upon chlorination were also investigated. Comparison of the results showed that the samples were different according to the origin of the sample, isolation procedure, and time of sampling. The differences are not the same for all parameters used. Standardized procedures have to be applied to redissolve the organic material in water in order to compare data. For the samples investigated, it was shown that parameters like elemental analysis (H/C ratio), the specific spectral absorption in the UV range, proton capacity, complexation capacity and anionic particle charge, amount of hydrolysable amino acids and carbohydrates, adsorption behaviour on activated carbon, and the THM-FP are sensitive parameters to show differences concerning origin and isolation procedure.     

Soil carbon stocks after conversion of Amazonian tropical forest to grazed pasture: importance of deep soil layers

Recent studies suggest that carbon (C) is stored in the topsoil of pastures established after deforestation. However, little is known about the long-term capacity of tropical pastures to sequester C in different soil layers after deforestation. Deep soil layers are generally not taken into consideration or are underestimated when C storage is calculated. Here we show that in French Guiana, the C stored in the deep soil layers contributes significantly to C stocks down to a depth of 100 cm and that C is sequestered in recalcitrant soil organic matter in the soil below a depth of 20 cm. The contribution of the 50–100 cm soil layer increased from 22 to 31 % with the age of the pasture. We show that long-term C sequestration in C4 tropical pastures is linked to the development of C3 species (legumes and shrubs), which increase both inputs of N into the ecosystem and the C:N ratio of soil organic matter. The deep soil under old pastures contained more C3 carbon than the native forest. If C sequestration in the deep soil is taken into account, our results suggest that the soil C stock in pastures in Amazonia would be higher with sustainable pasture management, in particular by promoting the development of legumes already in place and by introducing new species.     

Stable nitrogen isotopes (δ15N) in thalli of the lichen Hypogymnia physodes along a altitudinal gradient in the Khangai Plateau, Mongolia

Stable nitrogen isotopes (??¹⁵N) have been determined in the organic matter (OM) of thalli of the lichen Hypogymnia physodes (L.) Nyl. collected at 15 levels along an altitudinal gradient (1250?C2928 m a.s.l.) in forest and alpine meadow communities of the Khangai Plateau, Mongolia. The results show that, in the study region as a whole, no correlation between the ??¹⁵N content and elevation is observed. However, the lichen OM within the mountain forest belt is depleted of the heavy ¹⁵N isotope as elevation increases (from 1250 to 2400 m a.s.l.), whereas in the alpine meadow belt (2500?C2928 m a.s.l) it is enriched with this isotope. In addition, ??¹⁵N values in OM show an inverse dependence on the relative content of total nitrogen in the thalli.     

Distribution Of Cadmium And Nickel Among Various Forms In Natural And Contaminated Soils Amended With Edta

Because of its strong chelating capacity, application of ethylenediaminetetraacetic acid (EDTA) to soils may change the amount and distribution of heavy metals among their various chemical forms. Therefore, a greenhouse experiment was conducted using two cultivars of Brassica species (Brassica juncea and Brassica carinata) as hyper accumulator test crops on natural and artificially Cd and Ni contaminated soils. Both natural and metal amended soils were treated with disodium salt of EDTA at 0 and 1 g kg^–1 soil. After harvest of crops, soil samples were fractionated into water soluble plus exchangeable (WE), carbonate (CARB), organic matter (OM), Mn oxide (MnOX), amorphous Fe oxide (AFeOX), crystalline Fe oxide (CFeOX) and residual (RES) fractions. In metal amended soils, Cd and Ni were found predominantly in the AFeOX fraction in the absence of EDTA application and in the WE fraction in EDTA treated soil. Application of EDTA resulted in the redistribution of Cd among different forms and increased significantly Cd in the WE fraction with a concomitant significant decrease in the OM fraction. In natural soils, more than 40% of the total Cd was present in the RES fraction while in contaminated soil it was only 5%. Nickel in the WE fraction increased significantly while it considerably decreased in the CARB, OM, MnOX, AFeOX and CFeOX fractions with EDTA addition. This indicated that applied EDTA is capable to move Cd and Ni from the less soluble or more stable forms (CARB, OM, MnOX, AFeOX and CFeOX) to the most soluble form (WE). N natural soils, Ni in the RES fraction was found upto 49%, whereas only 10% of the total Ni was observed in contaminated soil, irrespective of EDTA treatment. In general, the amount of Cd recovered after harvest of both the Brassica cultivars did not differ significantly in any fraction except the WE fraction. The amount of Ni recovered in the AFeOX fraction was significantly higher after harvest of B. juncea as compared to B. carinata.Readers should send their comments on this paper to: BhaskarNath@aol.com within 3 months of publication of this issue.     

四湖地区渍害稻田土壤有机质及其氧化稳定性

采用定点调查和大田采样的方法，较系统地研究了不同渍害程度的稻田土壤有机质和活性有机质与土壤主要农化指标之间的关系。结果表明：(1)活性有机质与土壤全氮、碱解氮和速效磷等肥力指标间的相关系数均达极显著水平，且比土壤有机质与其对应肥力指标间的相关系数均要大，比有机质更能反映出土壤有效养分的供应。(2)从通径分析结果看出：碱解氮对活性有机质的直接效应要小于速效磷对活性有机质的直接效应，前者为27.3％，后者为46．1％。渍害土壤中与活性有机质关系最密切的土壤肥力指标是速效磷和碱解氮。(3)初步认为用有机质氧化稳定性(Kos值)比用有机质含量或活性有机质含量能够更好地作为渍害土壤判断渍害程度的标准。     

鄱阳湖生态区长期施肥对稻田土壤碳汇效应与固碳潜力的影响

在施肥条件下确定平衡状态时,土壤有机碳含量水平对于正确评价土壤的固碳潜力和制定合理的有机物质分配措施具有重要意义。分析了前人研究的江西省有机碳储量数据并采用Jenny模型对长期不同施肥下有机碳动态数据进行模拟。结果表明,鄱阳湖生态区有机碳储量占全省的46%,以鹰潭地区最高,九江地区最低。施肥明显增强了土壤的碳汇作用,单施有机肥或有机无机肥配施（70F+30M、50F+50M、30F+70M、NPKM、NPK+S、NPK+P和NPK+C）处理的土壤有机碳含量明显高于施化肥处理,以南昌县的30F+70M、进贤县的NPKM和余江县的NPK+P处理最高,其平衡时有机碳含量和固碳潜力分别较施化肥处理提高了3061%和6115%、3017%和5496%、3826%和7479%。因此,提高鄱阳湖生态区农田有机碳密度和固碳潜力最有效方法是有机无机肥配施,其配施方式以猪粪配施化肥相对最好,配施比例以70%有机肥配施30%化肥为宜     

The effect of fire on soil organic matter--a review

The extent of the soil organic carbon pool doubles that present in the atmosphere and is about two to three times greater than that accumulated in living organisms in all Earth's terrestrial ecosystems. In such a scenario, one of the several ecological and environmental impacts of fires is that biomass burning is a significant source of greenhouse gases responsible for global warming. Nevertheless, the oxidation of biomass is usually incomplete and a range of pyrolysis compounds and particulate organic matter (OM) in aerosols are produced simultaneously to the thermal modification of pre-existing C forms in soil. These changes lead to the evolution of the OM to "pyromorphic humus", composed by rearranged macromolecular substances of weak colloidal properties and an enhanced resistance against chemical and biological degradation. Hence the occurrence of fires in both undisturbed and agricultural ecosystems may produce long-lasting effects on soils' OM composition and dynamics. Due to the large extent of the C pool in soils, small deviations in the different C forms may also have a significant effect in the global C balance and consequently on climate change. This paper reviews the effect of forest fires on the quantity and quality of soils' OM. It is focused mainly on the most stable pool of soil C; i.e., that having a large residence time, composed of free lipids, colloidal fractions, including humic acids (HA) and fulvic acids (FA), and other resilient forms. The main transformations exerted by fire on soil humus include the accumulation of new particulate C forms highly resistant to oxidation and biological degradation including the so-called "black carbon" (BC). Controversial environmental implications of such processes, specifically in the stabilisation of C in soil and their bearing on the global C cycle are discussed.     

Soil and soil water studies at the HUMEX site

Changes to natural organic compounds by acid deposition and subsequent effects on Al mobilization are not well understood. The HUMEX catchment-scale acidification experiment in western Norway offers a unique possibility for an integrated assessment of these interactions. In this report, the soil and soil water chemical data from the HUMEX site, from before and after the onset of experimental acidification, are used to characterize the catchment. Changes in soil water chemistry are discussed and controls on dissolved organic carbon are addressed in relation to Al mobilization. Decreases in the concentration of dissolved organic carbon (DOC) and organic Al fractions were found in soil water after the treatment started. These changes were related to an increase in soil water sulphate concentrations. The sulphate levels showed a significant increase (on a 95% level) in four of ten soil horizons while nitrate remained nearly unchanged. In organic soils, where the dissolved organic carbon content was high, the major control for monomeric aluminum concentration appeared to be the amount of exchangeable aluminum in the soil. In mineral soils, the gibbsite dissolution may govern inorganic Al concentrations in soil water, though substantial undersaturation was found when DOC was high.     

The influence of the sorptive properties of organic soils on the migration rate of 137Cs

Using a compartment model, the migration rates of 137Cs were calculated for two types of organic soils: a low peat-muck soil and a black earth. The migration rates of 137Cs in the tested soils turned out to be significantly higher than in mineral types examined earlier and ranged from 0.6 to 12.3 cm/year. The partition coefficients (Kd) were also determined for samples with varying organic matter content (OM) that were taken from different layers of the studied soils. The experimental results indicate that there is a clear relationship between Kd values and OM. The investigation was widened by microcalorimetric measurements which confirmed that the adsorption of 137Cs on the organic soils is low.     

Distribution of organic carbon, selected stable elements and artificial radionuclides among dissolved, colloidal and particulate phases in the Rhône River (France): preliminary results

The behaviour of radionuclides discharged from nuclear facilities in the Rh?ne River depends on their distribution among the dissolved, colloidal and particulate phases. A large water sample was fractionated using sequential ultrafiltration. Size distributions of organic carbon, Fe, Al, Si, Ca, Mg, Cu, Zn, 137Cs, 60Co and 106Ru were obtained. Our results show that organic colloids account for 11% of the total organic carbon content. Approximately 20% of the dissolved (< 450 nm) Fe and Al are in colloidal classes. 137Cs is not significantly transferred by the colloidal phase while 25% of 60Co or 106Ru is associated with organic and inorganic colloids.     

香溪河流域不同介质中碳、氮、磷的分布特征及相关性研究

为了解香溪河流域碳、氮、磷的分布情况及水、陆生态系统中这些生源要素间的相互关系,对流域内河岸带土壤、河流水体及沉积物中总有机碳(TOC)、总氮(TN)、总磷(TP)含量进行调查,分析它们在流域内的分布特点,探讨各要素在3种介质间的相关性及随河流级别的变化规律。研究发现,超过60%的样点土壤中TOC、TN含量处于"较丰富"或"丰富"等级,耕地附近样点的TOC、TN和磷矿区附近样点的TP普遍偏高。河流水体及沉积物中各要素的含量都与土壤中的含量紧密相关,但水、陆介质间TP的相关性较TOC、TN强。低级别河流样点土壤中TOC、TN、C/P、N/P值和沉积物中C/P及N/P值整体较高级别河流样点高。结果表明:以磷矿开发和农业施肥为代表的人类活动,对香溪河流域内生源要素的含量及分布产生了显著影响;水体中P元素含量与陆源关系最强,在水体污染控制中应予以重视。     

Impact of woody encroachment on soil organic carbon and nitrogen in abandoned agricultural lands along a rainfall gradient in Italy

Land use changes represent one of the most important components of global environmental change and have a strong influence on carbon cycling. As a consequence of changes in economy during the last century, areas of marginal agriculture have been abandoned leading to secondary successions. The encroachment of woody plants into grasslands, pastures and croplands is generally thought to increase the carbon stored in these ecosystems even though there are evidences for a decrease in soil carbon stocks after land use change. In this paper, we investigate the effects of woody plant invasion on soil carbon and nitrogen stocks along a precipitation gradient (200?C2,500?mm) using original data from paired experiment in Italian Alps and Sicily and data from literature (Guo and Gifford Glob Change Biol 8(4):345?C360, 2002). We found a clear negative relationship (?0.05%?C?mm^?1) between changes in soil organic carbon and precipitation explaining 70% of the variation in soil C stocks after recolonization: dry sites gain carbon (up to +67%) while wet sites lose carbon (up to ?45%). In our data set, there seem to be two threshold values for soil carbon accumulation: the first one is 900?mm of mean annual rainfall, which separates the negative from the positive ratio values; the second one is 750?mm, which divides the positive values in two groups of sites. Most interestingly, this threshold of 750?mm corresponds exactly to a bioclimatic threshold: sites with <750?mm mean annual rainfall is classified as thermo-mediterranean sites, while the ones >750?mm are classified as mesomediterranean sites. This suggests that apart from rainfall also temperature values have an important influence on soil carbon accumulation after abandonment. Moreover, our results confirmed that the correlation between rainfall and trend in soil organic carbon may be related to nitrogen dynamics: carbon losses may occur only if there is a substantial decrease in soil nitrogen stock which occurs in wetter sites probably because of the higher leaching.     

城市湖泊富营养化对水生植物叶片C、N、P化学计量特征的影响

为研究城市湖泊富营养化对水生植物叶片元素组成的影响,在植物生长季,对南京3个湖泊的6种常见水生植物进行碳(C)、氮(N)、磷(P)生态化学计量学研究,并分析驱动水生植物叶片元素变化的关键环境因子。结果表明:(1)水生植物叶片C、N、P含量变化范围分别为397.03～672.70、10.63～39.16及1.15～13.30 mg/g,叶片C/N、C/P及N/P变化范围分别为13.15～50.36、31.39～458.60及1.88～19.06,其中叶片P含量变异最大,叶片C含量变异最小;(2) Spearman相关性分析表明,芦苇(Phragmites australis)、睡莲(Nymphaea tetragona)和金鱼藻(Ceratophyllum demersum)叶片元素组成与湖泊富营养化综合指数具有显著相关性,叶片P含量随湖泊富营养指数升高而增加,叶片C/P及N/P随之减小;(3) RDA分析表明,春季水生植物叶片C、N、P含量及C/N/P变化主要受水体高锰酸盐指数(COD_(Mn))和底泥总有机碳(SOC)含量的共同影响,夏季主要受水体总磷(TP_W)浓度的影响,秋季主要受底泥总磷(TP_S)含量的影响。     

Characterization of natural organic matter from eight Norwegian surface waters: Proton and copper binding

As a part of the International NOM-Typing Project, proton and copper binding studies were conducted on ultrafiltered (>1000 dal.) and dialysed (>100 dal.) natural organic matter (NOM) samples from eight Norwegian Lakes. The NOM samples were similar with respect to proton and copper binding, although minor differences were observed among the samples of different origin. Slight variations occurred for seasonal changes and lime additions. The proton binding pK_a values grouped in three distinct classes: pK_a1 = 4.20–4.28; pK_a2 = 6.61–6.87; and pK_a3 = 9.27–9.8. The average total proton binding site concentration of the NOM samples was: 12.7 meq/g total organic carbon (TOC). Two binding sites were established for copper with average log K1 = 4.84 and log K2 = 7.17. The average site concentration for samples isolated by reverse osmosis (RO) was 0.56 μmol/mg C. Copper binding characteristics appear to be influenced by the method of sample isolation. For NOM isolated by low pressure evaporation (evap), binding site concentrations are smaller, conditional stability constants are higher, variability of the copper complexation capacity is smaller, and correlation with elemental composition (C, N, H) is better than in the case of NOM isolated by RO.     

Effect of indigenous bacterial activity on arsenic mobilization under anaerobic conditions

Batch biochemical leaching tests were carried out to investigate the mobility of arsenic from a contaminated soil collected from a French gold mining site. The specific objective of this research was to examine the effect of indigenous bacterial activity on arsenic mobilization under anaerobic conditions. In a first step, physical and chemical characterizations were performed to provide data concerning the liquid-solid partitioning and mobility of arsenic and other inorganic constituents. In a second step, batch bioleaching tests were conducted in shaker flasks to determine the effect of indigenous bacterial activity under different anaerobic conditions (i.e., addition of mineral nutrients and carbon sources) on arsenic mobilization. Results indicated that arsenic release during contact with deionized water was limited by its very low solubility in the interstitial solution and by the stability of the different arsenic compounds formed with the amorphous solid phases of the soil (mainly iron (oxy)hydroxides). However, an increased mobilization potential was observed over the long term under anaerobic conditions with indigenous bacterial activity enhanced by the addition of carbon sources.