土壤磷酸盐的吸收对Cu2+二次吸附动力学的影响

The effects of sorbed phosphate on the kinetics of Cu^2 secondary adsorption on three major types of soils in southern and Central China were studied using the batch method and flow (or miscible displacement) techniques.Both of the methods showed that diffusions were the ratedetermining steps in the Cu^2 adsorption by the soils.By the flow method,the course of Cu^2 adsorption kinetics consisted of two steps-sn initial rapid process and a later slow process of Cu^2 adsorption;while by the batch method,the 90% of Cu^2 adsorption reaction was found to finish within first 1 minute.The results obtained using the flow method also indicated that for red soil and yellow-brown soil ,Cu^2 adsorptions during the initial reaction periods were restrained when the soils sorbed phosphate,whereas the adsorption reactions were stimulated at the final time,For grey Chao soil,sorbed phosphate retarded the Cu^2 adsorption in the whole reaction period.The results obtained using the batch method and low techniques all implied that the different effects of sorbed phosphate would be attributed to its effects on Cu^2 ion diffusion in soil solution.     

Biological decay of 18O-labeled phosphate in soils

There is an increasing demand to develop a means to trace phosphorus (P) movement through the environment as excessive inputs of P have led to the eutrophication of many fresh water bodies. ¹⁸O labeled phosphate has been suggested as a potential tool for tracing P, and other researchers are using information from natural abundance ¹⁸O levels of phosphate to study phosphorus cycling. The objective of this research was to determine the rate of biological de-labeling of ¹⁸O in soils. This objective was achieved using a laboratory incubation study in which three silt-loam textured soils were incubated with 250 mg kg⁻¹ P¹⁸O₄-P for a period of 3, 10, 30, or 50 d. The incubations were conducted on both sterilized and unsterilized soils. Following incubation, phosphate from soils was extracted with a modified Bray extractant and analyzed using electrospray ionization mass spectrometry to determine the distribution of labeled phosphate species. The half-life of P¹⁸O₄ in the non-sterile soils ranged from 15 to 22 d, while there was no observed P¹⁸O₄ de-labeling in sterile soils after 50 d. A parameterized numerical model was developed which provided insight into the dynamics of the individual labeled phosphate species, including their half-lives and relative concentrations across the incubation period. The use of P¹⁸O₄ may be useful in areas where use of radioisotopes of P is restricted, and P¹⁸O₄ has potential to be useful to elucidate the dynamics of the P cycle in soils.     

Phosphorus saturation in soils and groundwaters

On average, crops require about 30 kg ha⁻¹ y⁻¹ of P in humid regions. in some regions fertilizer and manure are applied in amounts that exceed this. the surplus of P in agricultural areas is about 20-45 kg ha⁻¹ y⁻¹. This implies an accumulation of P. the surplus of P estimated from the balance of agricultural soils of industrialized countries in Europe in the last four decades is between 800 and more than 1500 kg ha⁻¹ although this distribution is not even. Phosphorus accumulation is more than one order of magnitude higher than average in areas with intensive livestock farming. Consequently, The application of high levels of manure exceed the capacity of the soil to store P. This implies that P saturation May, pose a problem. Indeed, about half of the Dutch sandy soils (approximately 300 000 ha) are currently considered to be saturated with P, meaning that there is a hazard of P leaching to groundwaters in the future. Assuming current phosphate application rates, phosphate leaching is a distinct possibility over a period of decades to a century. Vulnerable areas are soils with high inputs, low sorption capacities for P, high water-tables and a low retention time for water. the possible consequence is a time-delayed increase of eutrophication of surface waters (lakes, rivers and the sea) caused by a diffuse load of P in the few next decades. Modelling the influence of different agricultural strategies shows that accumulation of P would not increase further only if the use of P increases by an amount that compensates for the increased inputs. It is proposed to change the current support system of agriculture by installing a system of financial incentives and taxes which seek to promote nutrient balances for each farm.     

培养温度和时间对磷肥在黑土中转化的影响

采用室内培养试验研究了培养温度和时间对磷酸二氢钙(MCP)、磷酸二氢铵(MAP)和磷酸氢二铵(DAP)在黑土中转化的影响。结果表明:温度升高增加了黑土对肥料磷的固定,且有利于Al-P的形成;培养50 d后,温度由5℃升至25℃时,We-P在添加MAP和MCP处理的土壤中占外源磷的比例分别降低51%和42%,同时Al-P分别上升110%和45%;在培养初期,温度对Ca8-P和Fe-P形成的影响不显著,但随培养时间的延长,差异显著。25℃时,培养时间对Ca2-P和Ca8-P形成的影响较小;Al-P在培养初期形成速率很快,随培养时间的延长,形成速率下降,而Fe-P的形成速率与之相反;Al-P的增加量与We-P的下降量呈显著线性正相关。与MAP和MCP相比,DAP更适合在黑土中施用。     

培养温度和时间对磷肥在黑土中转化的影响

采用室内培养试验研究了培养温度和时间对磷酸二氢钙(MCP)、磷酸二氢铵(MAP)和磷酸氢二铵(DAP)在黑土中转化的影响。结果表明：温度升高增加了黑土对肥料磷的固定,且有利于Al-P的形成;培养50 d后,温度由5℃升至25℃时, We-P在添加MAP和MCP处理的土壤中占外源磷的比例分别降低51%和42%,同时Al-P分别上升110%和45%;在培养初期,温度对Ca8-P和Fe-P形成的影响不显著,但随培养时间的延长,差异显著。25℃时,培养时间对Ca2-P和Ca8-P形成的影响较小;Al-P在培养初期形成速率很快,随培养时间的延长,形成速率下降,而Fe-P的形成速率与之相反;Al-P的增加量与We-P的下降量呈显著线性正相关。与MAP和MCP相比,DAP更适合在黑土中施用。     

Influence of residual phosphate fertilizer on labile and extractable zinc in hawaii soils

Abstract

Zinc availability was studied using five soils from Hawaii which had histories of massive phosphorus applications. Heavy phosphate fertilization usually increased extractable Zn, irrespective of the extractant used. The extra extractable Zn associated with the added P probably came from Zn as an accessory element in the fertilizer. Treble superphosphate commonly used in Hawaii contains about 1400 ppm Zn. The Zn content of phosphate fertilizers must be considered before making statements about the effect of fertilizer P on Zn solubility and availability in soils.

Two solutions (0.1N HCl and 0.005M DTPA) were compared as Zn extractants for Hawaii soils. DTPA extracted less Zn than 0.1N HCl. Zinc extracted by repeated HCl treatment was more closely related to the labile Zn pool (E‐values and L‐values) than was DTPA‐extractable Zn. The results suggest that 0.1N HCl extractable Zn, Zn E‐value and Zn L‐value measured the quantity of a single fraction of soil Zn.

Repeated extraction of soil with 0.1N HCl seems to be a suitable procedure for evaluating the Zn status of acid, highly weathered soils of Hawaii.     

尿素向氨基糖的转化以及对土壤氨基糖库动态的影响

采用13CO(NH2)2为底物进行黑土培养实验,利用气相色谱/质谱技术测定土壤中三种氨基糖含量以及同位素富集比例,根据其微生物标识物作用探讨土壤中不同微生物群落对于尿素碳的同化利用特征及黑土氨基糖库对于尿素添加的响应。研究结果表明,尿素碳可以被土壤微生物同化利用,但是可利用性显著低于葡萄糖。氨基葡萄糖中13C富集比例显著高于胞壁酸,表明真菌对尿素碳的同化能力高于细菌。尿素添加使土壤有机碳含量有所下降,同时土壤氨基糖总量及其与有机碳的相对比例也显著降低,说明在碳源严重受限条件下,氨基糖可被优先分解利用以补充碳源供给。胞壁酸含量虽低,但其调节并平衡碳氮元素供给与需求的能力较强;氨基葡萄糖稳定性高于胞壁酸,但在碳源缺乏时也可部分分解。土壤氨基糖的动态与土壤碳氮的可利用性及其耦合作用密切相关,在平衡土壤碳氮需求方面具有一定的调节作用。     

Effects of equilibrating salt solutions on phosphate sorption by soils

Abstract

Several equilibrating salt solutions have been used in the studies of P sorption by soils and sediments. This study was conducted to evaluate the effects of 10 salt solutions on estimation of P sorption by soils. Results obtained showed that, when the equilibrating solution was made to contain 0.01M with respect to CaCl₂, Ca(NO₃)₂, CaSO₄, MgCl₂, KCl, LiCl, Nacl, or KHCO₃, the amount of P sorbed by soil always exceeded the amount sorbed from the soil‐water system. In comparison with the amount of P sorbed from water, 0.01M NaHCO₃ reduced P sorption by soils. Use of THAM buffer (0.05M pH 7.0) to control the pH increased P sorption by some soils and decreased P sorption by others, relative to that sorbed from the soil‐water system. The results indicated that inclusion of salts in the equilibrating solution for P‐sorption studies should be avoided, especially in studies related to water quality.     

Stability and transport of titanium dioxide nanoparticles in three variable-charge soils

Journal of Soils and Sediments - The exposure pathways and environmental impacts of titanium dioxide nanoparticles (TiO2 NPs) released into soils could be significantly influenced by their...     

低分子量有机酸对石灰性土壤磷素形态转化及有效性的影响

采用室内培养和化学分析的方法研究了几种低分子量有机酸对石灰性土壤中磷的活化作用。结果表明:供试有机酸通过溶解、螯合等作用均能不同程度地促进合成磷酸盐的磷素释放。活化DCP、ODP、Fe-P、A l-P的能力依次为柠檬酸>草酸>苹果酸>酒石酸>乙酸;活化FA的能力是草酸>柠檬酸>苹果酸>酒石酸>乙酸。同种有机酸作浸提剂时,有机酸浓度越高磷酸盐中磷素释放量也越大。施加各种有机酸可以不同程度地降低土壤中Fe-P、A l-P和Ca10-P,增加Ca2-P、Ca8-P和O-P含量,总的趋势是促进土壤中植物难以利用的无机磷形态向有效性较高的形态转化。这种促进作用大小顺序为草酸>柠檬酸>酒石酸。     

Transformation of organic matter and clay minerals in cultivated gray forest soils

Mechanisms of the agropedogenic transformation of cultivated gray forest soils are discussed. It is shown that the loss of organic carbon from these soils upon their cultivation is mainly due to the intense mineralization of an easily decomposable fraction having a density of less than 2 g/cm³ and a characteristic size above 50 μm. Simultaneously, a certain portion of soil microaggregates is destroyed. Several additional indices of the processes of soil erosion and sediment accumulation on the soil surface (soil aggradation) are suggested. These indices take into account the character of soil clay minerals and soil organic matter. Indicative characteristics of the second humus horizon are suggested on the basis of published materials and new analytical data.     

Transformation of clay minerals in nanoparticles of several zonal soils in China

Purpose

Clay minerals significantly affect the physical, chemical, and biological processes of soils. They undergo spontaneous modification and transformation depending to the climatic conditions. Information concerning the compositions and transformation of clay minerals in nanoparticle colloids (NPs) (25–100 nm) is severely lacking. Studying clay mineral transformation is important approach to understand soil formation. This study was conducted to determine the transformation sequence of clay minerals in several zonal soil NPs.

Materials and methods

Four soils (Haplustalf, Alf-1; Hapludalf, Alf-2; Hapludults, Ult-1 and Ult-2) were collected from B horizons developed under three different climatic zones of China. Alf-1 (36° 05′ N and 117° 24′ E) was located under a warm temperate zone and Alf-2 (30° 38′ N and 115° 26′ E), Ult-1 (29° 13′ N and 113° 46′ E), and Ult-2 (19° 27′ N and 109° 17′ E) under a subtropical zone. The clay particles (<?2000 nm) (CPs) and nanoparticles (25–100 nm) (NPs) of tested soils were separated. The element composition of CPs and NPs was identified by microwave digestion method. The mineralogy and chemical bonding of clay minerals were studied by X-ray diffraction (XRD) and Fourier transform infrared spectroscopy (FT-IR).

Results and discussion

With decreasing latitude, NPs and CPs showed that the molar ratio of SiO₂ to Al₂O₃ trends to diminish, indicating the phenomenon of desilication and allitization in the tested soils. XRD analysis revealed that the main clay mineral of Alf-1 NPs was illite, followed by vermiculite, kaolinite, and kaolinite interstratified minerals (KIMs). The clay minerals of Alf-2, Ult-1, and Ult-2 NPs were dominated by kaolinite (and KIMs), followed by illite, with a little content of hydroxyl-interlayered vermiculite (HIV) in Ult-1 NPs and trace content of gibbsite in Ult-2 NPs. With decreasing latitude, vermiculite and HIV decreased in NPs. When compared to CPs, smectite as well as illite-vermiculite mix-layer mineral (I-V) and illite-HIV mix-layer mineral (I-HIV) were not detected in NPs. The analysis of d060 region by XRD showed that with decreasing latitude, the main clay minerals in NPs were dioctahedral minerals (e.g., illite or kaolinite). These clay minerals resulted from the transformation of trioctahedral minerals in CPs. The disappearance of 2:1 swelling minerals and trioctahedral minerals showed that the NPs were more susceptible to weathering than CPs.

Conclusions

With decreasing latitude, the transformation of clay minerals followed the sequence of illite?→?HIV?→?kaolinite?→?gibbsite in tested NPs.

     

磷酸铵在三种典型土壤中的转化及其有效性

研究了磷酸二氢铵(MAP)和磷酸氢二铵(DAP)在3种典型土壤中的转化,并评价了其有效性.结果表明:施用磷酸铵可改变肥际微域土壤的pH值,并且这种效应可持续几个月;MAP在黑土中,反应产物主要为Al-P,占38.8%,其次为Fe-P,占12%;在潮土中,Ca_2-P是主要形态,占34%,其次为Ca_8-P,占28%;在水稻土中,We-P是主要形态,占50%以上,其次为Ca_2-P,占20%.在黑土中We-P在DAP处理中所占的比例较MAP处理中高,而Al-P和Fe-P所占的比例正好与之相反;在最初的10 d里,We-P下降显著,随反应时间延长,DAP和MAP处理间We-P所占的比例差异减小;MAP在水稻土中的有效性最高,其次是潮土和黑土;在黑土中DAP的有效性较MAP要好,MAP主要转化成了Al-P.     

六氯苯在土壤中的主要迁移转化过程

六氯苯(HCB)是环境中典型的持久性有机污染物(POPs)。土壤是HCB的主要贮存场所,研究土壤中HCB的迁移转化规律对揭示其环境效应有重要意义。本文从以下几方面综述了土壤中HCB的主要迁移转化过程:土壤中累积的HCB不断向大气挥发而造成空气污染;土壤对HCB的吸附影响其在环境中的迁移转化速率;HCB通过多种化学键与土壤形成结合残留,暂时降低其生物有效性;厌氧条件下,HCB可发生还原脱氯降解,使其毒性和持久性大大降低。本文最后展望了关于土壤中HCB迁移转化的下一步研究方向。     

冻融交替对土壤氮素转化及相关微生物学特性的影响

土壤冻融是发生在中、高纬度及高海拔地区的一种常见的自然现象。冻融作用通过影响土壤物理性质及生物学性状进而对土壤氮素转化过程产生重要影响,但目前关于冻融作用对土壤氮素转化过程影响的研究结果还不尽一致,对于冻融作用下土壤微生物学特性的研究相对较少。本文着重论述了冻融作用对土壤氮素转化过程(有效氮素含量变化、氮素净矿化速率、氮素损失途径等)的影响,并对冻融作用下土壤微生物生理和代谢特性进行了归纳和总结,简要指出目前研究过程中存在的问题,并对未来研究方向提出展望。     

Mechanisms of increase in content of water-soluble P in Hachirogata reclaimed soils after NaCl washing

Abstract

In some of the drainage waters in Hachirogata reclaimed land, a very high concentration of inorganic P (up to 2 mg P L^-1) has been recently detected (Sato et al. unpublished). The drainage waters flow into the Lake Hachirogata that surrounds the land. Since the lake is also a reservoir, the water circulates through a closed system. Recently, the eutrophication of the lake has been found to be significant (Akita Prefectural Government 1989) and drainage water has been incriminated as one of the P sources of eutrophication. Therefore, it would be important to analyze the mechanisms responsible for the increase of P release from Hachirogata reclaimed land.     

可变电荷土壤黏粒表面带电点与离子相互作用的Wien效应表征

To investigate the interactions of oppositely charged sites on the surfaces of variable-charge soil particles with cations and anions, and to evaluate the mean Gibbs free binding and adsorption energies of various cations on particles of red soil and latosol, clay fractions smaller than 2 μm were separated from samples of the two variable-charge soils. Ferric oxides were removed from part of the clay fractions, which were then saturated with various chlorides (NaCl, KCl, CaCl2, CdCl2 or LaCl3). Electrical conductivities (EC) of dilute suspensions of the original and of the iron oxides-free clay fractions in deionized water were measured with the SHP-2 short high-voltage pulse apparatus, which enables measurement of the Wien effect at field strengths (E) from 14 to 250 kV cm-1. The Wien effect (EC-E) curves revealed EC increases of red soil suspensions between 14 to 200 kV cm-1, of 8.3, 8.4, 12.1, 5.9, and 1.2 μS cm-1 for NaCl, KCl, CaCl2, CdCl2, and LaCl3, respectively, reflecting the differing interactions with the various cations and chloride. The EC increments with the iron-free red soil suspensions were higher, being 29.7, 17.2, and 15.3 μS cm-1 for NaCl, CaCl2, and CdCl2, respectively. In the natural latosol suspensions the EC increments were practically zero, whereas in the iron-free fractions there were significant EC increments of 10.3, 5.7, 5.0, and 1.6 μS cm-1 for NaCl, CaCl2, CdCl2, and LaCl3, respectively.     

磷在潮土肥际微域中的迁移和转化

采用室内土柱实验研究了磷在潮土肥际微域中的迁移和形态转化。结果表明,磷在潮土中的移动距离很短,经过7 d和28 d的迁移,磷的迁移距离仅为8～14 mm。施入的磷主要固定在紧靠施肥点2 mm土体范围内,随距施肥点距离的增加,土壤水溶性磷、酸溶性磷和有效磷的含量呈指数曲线迅速降低。磷在施肥后7 d内的迁移量较大,迁移进入土壤的磷绝大部分被吸附固定。施肥量对不同形态磷在肥际微域中的迁移量产生显著影响;但培养时间只明显影响了水溶性磷的迁移量。     

Effects of sorbed orthophosphate on zinc status in three soils of eastern Canada

P-Zn interactions can affect fertilizer use and produce Zn deficiencies with certain crops. Phosphorus-Zn sorption-desorption reactions were studied in topsoil and subsoil samples from three Quebec soils. Soils were equilibrated with P solutions, then with Zn solutions, and finally with solutions containing no P or Zn. The first equilibration evaluated P sorption (P_s), the second evaluated Zn sorption (Zn_s) after P sorption (P_s), and the third evaluated Zn desorption (Zn_D) as related to added P. Subsequently, Zn fractions were extracted sequentially with KNO₃ (Zn _{kno 3}), NaOH (Zn_NaOH) solutions and concentrated HN0₃+ H₂0₂(Zn_HNO,).
One mmole sorbed P resulted in increases of 0.5 to 1.0 meq (mean = 0.72) increases in cation exchange capacity (CEC). Increased Zn_s with added P was equivalent to 4 to 5% of the increase in CEC induced by P_s in the Uplands (sand) and St. Bernard (loam) soils, and 0.4 to 0.9% in the Dalhousie (clay) soils, while one meq increase in CEC resulted in 1.5-3.5% decrease in Zn_D. There existed positive correlations between P_s and extractable soil Fe materials. Phosphate sorption enhanced associations between Zn_s, Zn_D or Zn fractions and soil organic or crystalline Fe contents, confirming that P addition increased specific sorption of Zn on Fe components. Other mechanisms including precipitation, P-induced negative charge and 'bridge' effects are also discussed.     

On the determination of total heavy metal content in saline soils and soils rich in organic matter

Abstract

Methods of soil decomposition for determination of heavy metal total content were considered. Two saline soils (chloride and sulphate solonchak solonetz) and one rich in organic matter were uzed for investigation. It has been established that decomposition by using HF‐HCl with a preliminary ignition at 500°C is a very suitable method. The type of the studied soils and the results obtained allow for this method to be recommended for decomposition of various soils.

On the basis of experiments with modelled soils it has been proved that possibilities for heavy metal losses on ignition are created when NaCl content and the percentage of weakly bound heavy metals (water‐soluble, exchangeable, etc.) are high. Under the conditions of the experiment (acid soils ‐ pH 4.3 and 5.0) losses of Zn and Pb but not of Cu have been incurred. Although these cases are not typical, this requires the applicability of the method for such particular occasions to be checked.