Redox condition and nitrate change in a newly flooded rice soil under percolation as influenced by oxidative iron and manganese

Nitrate leaching from intermittently flooded rice fields contributes to nitrate pollution in groundwater. In this study, redox conditions and nitrate change in a newly flooded rice soil under the influence of oxidative iron (Fe) and manganese (Mn) were investigated using flooded soil columns under moderate percolation (4.2?mm?d^?1). The amendments of α-Fe₂O₃ and β-MnO₂ powder (5 and 2.7?mg?g^?1, respectively) delayed the establishment of reducing conditions and lowered the rate of nitrate removal in the soil column, and subsequently increased the percolation of soil indigenous nitrate (8.3?mg nitrogen [N]?kg^?1) from 2.0% to 8.0%, and the percolation of externally amended nitrate (250?mg?N?kg^?1) from 11.0% to 26.0%. The pool of oxidative iron-centered metal oxidants needs to be jointly considered with the availability of organic carbon and hydrological conditions in evaluating redox conditions and nitrate change in intermittently flooded rice soils.     

Comparison of redox potential dynamics in a diked marsh soil: 1990 to 1993 versus 2011 to 2014

As revealed by an earlier study, young diked marsh soils on the west coast of Schleswig‐Holstein (Germany) are characterized by pronounced redox potential (E_H) dynamics. Since soil forming processes occur over a short period of time in these man‐made environments, the impact of pedogenesis on E_H was examined by comparing the E_H dynamics measured from November 1989 to October 1993 (weekly measurements) with those measured from November 2010 to October 2014 (hourly measurements) at the same study site in Polder Speicherkoog, Northern Germany. In addition, the necessity for high resolution E_H measurements was assessed as well as the impact of climate change on E_H. Redox potentials were determined in both monitoring campaigns with permanently installed platinum electrodes at 10, 30, 60, 100, and 150 cm soil depths. Soil properties were determined in November 1989 and in August 2013. In 24 years of soil formation, bulk density was demonstrated to increase by 28.5% and 33.3% in 10 and 20 cm depths, respectively, and the sulfide‐bearing Protothionic horizon lowered from 105 to 135 cm below surface level. Overall, E_H dynamics were similar at all soil depths during both study periods with topsoil compaction not affecting E_H. Annual alterations of E_H were primarily driven by the variable climatic water balance (CWB) and by the corresponding water table (WT) fluctuations. These fluctuations resulted in occasional aeration of the subsoil and subsequent oxidation of sulfides. A forecast of CWB to 2100 predicts an intensified WT drawdown by elevated evapotranspiration rates that should amplify sulfide oxidation. To deduce the soil redox status on a seasonal or annual scale, readings taken at daily intervals are sufficient. To identify biogeochemical processes, it is necessary to monitor E_H on an hourly basis because increases in E_H values of up to 540 mV have been observed within a 24 hour period in temporarily waterlogged horizons.     

Measurement of redox potential inside a suction probe

Ceramic suction probes were combined with internal redox electrodes in order to reduce the deviation between site parallels, and to relate redox potential measurements directly to the solution analyzed chemically. In a laboratory experiment soil material was water‐saturated for 49 days and temporal changes of redox potential and pH outside and inside the ceramic suction probes were recorded. Furthermore, iron concentrations inside the ceramic cups were detected. Results indicate that a device combining ceramic suction probes and redox electrodes is in principal possible. However, the device used here could not reduce the deviation between site replications compared to free installed redox electrodes. Increasing iron concentrations due to decreasing redox potentials outside and inside the ceramic suction probes indicate that the soil water iron dynamic is at least partly measurable using this device.<?show $6#>     

In situ long‐term redox potential measurements in a dyked marsh soil

The long‐term measurement of soil redox potential (E_H) by permanently installed Pt electrodes may be restricted by electrode breakdown (electrode rupture and resin leakage) and contamination, especially under wet and strongly reducing soil conditions. The E_H of a slightly alkaline (pH 7.1 to 7.3) Calcaric Gleysol developed from marine sediment in the dyked marsh of Schleswig‐Holstein, Northern Germany, was monitored weekly during a 4‐year period using permanently installed Pt electrodes. Measurements were performed in fivefold at 10, 30, 60, 100, and 150 cm. Furthermore, water table level was recorded. Sulfide occurred in 150 cm as a heritage of the previous marine environment. Mean water table level was 84 cm below the soil surface but was characterized by both short‐term and seasonally strong fluctuations. Levels of water table ranged from 33 to >200 cm below soil surface. In consistence with water table level, the E_H continually decreased with soil depth. Mean redox conditions were oxidizing at 10 (550 mV) and 30 cm (430 mV), weakly reducing at 60 cm (230 mV), and moderately reducing at 100 (120 mV) and 150 cm depth (–80 mV). Soil hydrology differed markedly during the study as expressed by periods of water saturation for each depth. This was reflected by Pt electrodes response, since period of water saturation and E_H were significantly negatively correlated as calculated for each year and depth (r_s = –0.971; n = 20; P < 0.01). The 60‐cm depth was most frequently influenced by water table fluctuations, showed the largest E_H range (920 mV) and the most distinct seasonal pattern in E_H. Good function of the electrodes in this depth can be concluded even after long time of installation in soil. Although established in a sulfide‐bearing environment, three of five electrodes at 150 cm showed a substantial increase (+500 mV) in E_H during summer of the third and fourth years of investigation, which had low water tables. It is not clear whether the non‐response of two electrodes was due to electrode contamination or spatial variation in E_H. When operating in reducing systems, this problem can be circumvented by installing a large number of electrodes or by a regular replacement of electrodes. Using properly constructed and permanently installed Pt electrodes, soil E_H can be monitored for extended periods under wet and reducing soil conditions.     

Rice-soil interactions in Vietnamese acid sulphate soils: impacts of submergence depth on soil solution chemistry and yields

Abstract. The aim of this study was to investigate the effects of water submergence depth on radial oxygen loss (ROL), soil solution chemistry and rice growth performance in acid sulphate soils in southern Vietnam. ROL was measured in a solution culture. In a separate pot experiment the impact of water submergence depth on rice growth and soil solution chemistry was studied. Three submergence depths were used in the two experiments (5, 10 and 15 cm). ROL declined with submergence depth and was significantly greater in young roots (with no root hairs) than in older roots. In the pot experiment rice growth and soil solution chemistry were clearly affected by the submergence depth. During the first crop at 5 cm submergence, there was a significantly higher yield and a higher oxidation state (pe+pH) compared to 10 or 15 cm submergence. The Fe concentration was significantly greater at the 5 cm depth compared to the 10 or 15 cm depth. SO₄^2– reduction was delayed at the 5 cm depth. Rice yield was c. 25% less at the 15 cm than at the 5 cm depth. During a second crop, there was a substantial SO₄^2- reduction and H₂S formation and almost no significant effects of submergence depth on either soil solution chemistry or crop yield. In a field experiment with a dry-season rice crop, yield and Fe, Al and SO₄^2– concentrations were higher at a shallow submergence depth than at greater depths in the same field, showing similar depth trends to those found during the first crop in the pot experiment. Farmers should be advised to use a shallow submergence depth and, if possible, avoid deep-rooted rice varieties. A conceptual model is suggested, which summarizes the relationships between ROL and soil solution chemistry.     

The composition of mobile matter in a floodplain topsoil: A comparative study with soil columns and field lysimeters

Floodplain soils are characterized by frequent and extreme redox changes caused by inundation with river water or imbibition of groundwater. Depending on the duration and extent of inundation, biogeochemical processes run at sub‐/anoxic conditions, which may result in the mobilization and relocation of dissolved and particulate matter within the soil. In this study, we investigated the effect of inundation events on the composition of mobilized matter in the topsoil horizon of a floodplain soil. We conducted experiments with soil columns in the laboratory and gravitational lysimeters in the field to identify redox‐mediated (im)mobilization processes and to estimate their relevance under field conditions. The lysimeters were filled with topsoil monoliths and run under in situ conditions during a ≈ 2.5‐y period. The soil columns were run with the same soil material either under strictly anoxic or mixed oxic–anoxic conditions. Effluents from mixed oxic–anoxic soil were composed fundamentally different [comparably high: Mn, Al, nitrate, sulfate; comparably low: pH, organic C (OC); not detected: Fe, As] compared to effluents from strictly anoxic soil (comparably high: pH, Fe, Mn, OC, As; comparably low: Al; not detected: nitrate, sulfate). Matter, which was mobile under anoxic conditions (e.g., Fe, As, OC), was effectively immobilized as soon as the mobile phase passed anoxic–oxic boundaries within soil (exception: Mn). We assume that the solution in the soil monoliths always passed such anoxic–oxic boundaries during downwards migration independent of lysimeter flooding with river water. This is indicated by the similar composition of the lysimeter seepage water and the effluents from mixed oxic–anoxic soil columns. Both solutions contained “fingerprints” from anoxic (Mn) and oxic conditions (nitrate). Inundations with river water and the duration of these floods (1–22 d) did not affect the composition of the lysimeter seepage water. In conclusion, immediate changes in the composition of the solution, which enters either the subsoil or nearby receiving waters, cannot be expected from regular topsoil flooding.     

Effect of sulfate on nitrate transport in volcanic ash soils sampled from the A and the B horizons

Intensive cultivation of crop fields using agricultural chemicals and fertilizers has led to changes in ecological systems, resulting in a high possibility of environmental pollution by contamination, or occasional reactions not only in the soil but also in the water and the atmosphere. Some substances are known to be very toxic to human beings at low concentrations. For example, nitrosamines are believed to be carcinogenic and mutagenic.     

Alleviation of manganese toxicity and manganese-induced iron deficiency in barley by additional potassium supply in nutrient solution

Barley plants were grown hydroponically at two levels of K (3.0 and 30 mm) and Fe (1.0 and 10 μm) in the presence of excess Mn (25 μm) for 14 d in a phytotron. Plants grown under adequate K level (3.0 mm) were characterized by brown spots on old leaves, desiccation of old leaves, interveinal chlorosis on young leaves, browning of roots, and release of phytosiderophores (PS) from roots. These symptoms were more pronounced in the plants grown under suboptimal Fe level (1.0 p,M) than in the plants grown under adequate Fe level (10 μm). Plants grown in 10 μm Fe with additional K (30 mm) produced a larger amount of dry matter and released less PS than the plants grown under adequate K level (3.0 mm), and did not show leaf injury symptoms and root browning. On the other hand, the additional K supply in the presence of 1.0 μM Fe decreased the severity of brown spots, prevented leaf desiccation, and increased the leaf chlorophyll content, which was not sufficient for the regreening of chlorotic leaves. These results suggested that the additional K alleviated the symptoms of Mn toxicity depending on the Fe concentration in the nutrient solution. The concentration (per g dry matter) and accumulation (per plant) of Mn in shoots and roots of plants grown in 10 μm Fe and 30 mm K were much lower than those of the plants grown in 10 μm Fe and 3.0 mm K, indicating that additional K repressed the absorption of Mn. The concentration and accumulation of Fe in the shoots and roots of the plants grown in 10 μm Fe and 30 mm K were higher than those of the plants grown in 10 μm Fe and 3.0 mm K, indicating that the additional K increased the absorption of Fe under excess Mn level in the nutrient solution. The release of PS, chlorophyll content, and shoot Fe concentration were closely correlated.     

pH与石灰性水稻土铁氧化还原过程的关系

光照和pH是调控土壤铁氧化物厌氧生物氧化还原的关键环境因素。本文采用恒温厌氧培养试验研究了黑暗、光照条件下土壤pH的变化及pH对铁氧化还原的影响,探索了pH与Fe(II)和水溶性无机碳的关系。结果表明,光照可改变土壤厌氧培养过程中pH的变化趋势,避光培养时土壤pH呈降低趋势,光照时呈先降低后增加趋势。pH介于4~9之间均可发生铁的还原反应,pH=7时还原量最大,128.5μmol g-1,pH调至4和9均可抑制避光条件下的铁还原。光照条件下pH 6~8时可发生Fe(II)的再氧化,控制初始pH为7时可使其再氧化量增加77.13%,达49.17μmol g-1。厌氧培养过程中Fe(II)与水溶性无机碳在避光时存在显著线性正相关关系,pH与Fe(II)和水溶性无机碳之间均存在显著线性负相关关系。     

Effect of moisture variation on sulfate concentration in a buck solonetz soil

Abstract

Sulfate concentration in the equilibrium solutions of a black solonetz soil was different at each moisture content. In the sub‐surface horizons a decrease in soil moisture up to about 35 percent resulted in a gradual increase of sulfate concentration. However, with further decrease in moisture the sulfate concentration increased abruptly. Variation of sulfate concentration appears to alter significantly certain cation ratios in the equilibrium solutions.     

Effects of sulfur,zinc, iron,copper, manganese,and boron applications on sunflower yield and plant nutrient concentration

Abstract

Sulfur, zinc, iron, copper, manganese, and boron application did not affect the seed yield or oil percentage of sunflower (Hilianthus annuus L.) on both dryland and irrigated soils in North Dakota in 1981. Field averages indicated significant Zn, Mn, and B uptake by sunflower at the 12‐leaf stage as a result of fertilization with these elements. Increased Zn uptake was also observed in the uppermost mature leaf at anthesis from zinc fertilization.

Although sunflower yield from boron fertilization was not significantly different from the check, a trend was observed in which boron fertilization seemed to decrease sunflower yield. Sunflower yields from the boron treatment were the lowest out of seven treatments in three out of four fields. Also, sunflower yield from the boron treatment was significantly lower than both iron and sulfur treatments when all fields were combined.     

分光光度法测定有机肥料中铜、铁、锌、锰含量

探索用分光光度法测定有机肥料中的微量元素铜(Cu)、铁(Fe)、锌(Zn)、锰(Mn)含量,并研究了显色反应的酸度条件、干扰因素及消除方法。该检测方法简单快速,可应用于有机肥生产企业中微量元素铜、铁、锌、锰的测定。     

Soil biological and physiochemical factors limiting the growth potential of tomato planted in waterlogged volcanic soil

Abstract

Many vegetable growers in Japan practice a unique waterlogged cultivation method with ample nitrogen (N) supply and microbial supplements, reporting vigorous plant growth, no soilborne diseases, and high yields. We simulated waterlogged soil conditions in greenhouse experiments to examine effects of soil pH and redox potential (Eh) as well as microbial influence on the growth of tomato seedlings. Soil pasteurization enhanced seedling growth whether the acidic, volcanic soil was waterlogged or well-drained. Among various antimicrobials, only soil treatment with polymyxin B improved shoot growth in nonpasteurized soil. The seedlings grew best in pasteurized acidic, waterlogged soil fertilized with ample potassium nitrate (KNO₃), which maintained soil Eh above zero. In nonpasteurized soil, growth was severely stunted by raising soil pH progressively to 8.5 while Eh dropped to –194?mV. The results suggested that heat-sensitive Gram-negative soil bacteria and low soil Eh were key factors limiting the growth potential of tomato plants in waterlogged soils.     

旱地土壤硝态氮与氮素平衡、氮肥利用的关系

利用长期肥料试验资料研究了土壤氮素平衡、氮肥利用率和土壤硝态氮之间的相互关系。结果表明,小麦不同施肥处理的氮肥利用率（NUE）为30.9%~65.8%,平均53.6%;土壤硝态氮累积率2.3%~44.1%,平均13.2%;氮素表观损失率25.0%~42.7%,平均33.2%。一般情况下,氮素盈余值与氮肥用量呈正相关,与磷肥用量呈负相关;土壤中硝态氮的数量与氮素盈余值呈正比,与氮肥利用率呈反比。黄土旱塬地区,小麦在经济合理施氮条件下,氮素盈余值为13.79 kg/hm2,硝态氮累积量为23.00 kg/hm2,说明过量施用一定数量的氮肥对保持作物生产力和土壤氮素营养是必要的。     

Ferric iron transformation in soils with rotation of irrigated rice-upland crops and effect on soil tillage properties

We examined the relationship between the form of iron and the tillability (defined as the degree of ease of pulverizing a soil into small clods) of soils in upland fields that had been converted from paddy fields. The amount of iron (Fe.e) extractable with acetate buffer (pH 3.0) decreased from 0.959 g kg_-1 in a field that has been continuously used as a paddy field to 0.104 g kg-I in a field that had been converted into an upland field for a period of 5 y. There was no significant change in the free iron oxide content under upland conditions. These results indicate that ferric iron oxides are gradually crystallized to less reactive forms after the conversion of a paddy field into upland conditions. Both soil tillability (represented by the mean clod diameter after tillage) and the stability of the soil microstructure (represented by the sediment volume) also increased during the 3-y period after conversion and then remained constant for the last 2-y period of the study. On the basis of these results, two mechanisms for the improvement of soil tillability can be proposed as follows: crystallization of ferric iron oxides increased their resistance to microbiological reduction and due to this stabilization the iron oxides as a cementing reagent that contributed to the soil microstructure, which in turn affected the soil tillability. During the first year after drainage, however, there was no significant correlation between the soil tillability and amount of Fe_ac, presumably because the soil was not sufficiently dry in the first year after conversion, and the iron oxides did not affect appreciably the soil structure.     

Competition for electron donors among nitrate reducers,ferric iron reducers,sulfate reducers,and methanogens in anoxic paddy soil

Slurries of anoxic paddy soil were either freshly prepared or were partially depleted in endogenous electron donors by prolonged incubation under anaerobic conditions. Endogenous NO ₃ ^– was reduced within 4 h, followed by reduction of Fe³⁺ and SO ₄ ^2– , and later by production of CH₄. Addition of NO ₃ ^– slightly inhibited the production of Fe²⁺ in the depleted but not in the fresh paddy soil. Inhibition was overcome by the addition of H₂, acetate, or a mixture of fatty acids (and other compounds), indicating that these compounds served as electron donors for the bacteria reducing NO ₃ ^– and/or ferric iron. Addition on NO ₃ ^– also inhibited the reduction of SO ₄ ^2– in the depleted paddy soil. This inhibition was only overcome by H₂, but not by acetate or a mixture of compounds, indicating that H₂ was the predominant electron donor for the bacteria involved in NO ₃ ^– and/or SO ₄ ^2– reduction. SO ₄ ^2– reduction was also inhibited by exogenous Fe³⁺, but only in the depleted paddy soil. This inhibition was overcome by either H₂, acetate, or a mixture of compounds, suggesting that they served as electron donors for reduction of Fe³⁺ and/or SO ₄ ²⁺ . CH₄ production was inhibited by NO ₃ ^– both in depleted and in fresh paddy soil. Fe³⁺ and SO ₄ ^2– also inhibited methanogenesis, but the inhibition was stronger in the depleted than in the fresh paddy soil. Inhibition of CH₄ production was paralleled by a decrease in the steady state concentration of H₂ to a level which provided a free enthalpy of less than G=–17 kJ mol^-1 CH₄ compared to more than G=–32 kJ mol^-1 CH₄ in the control. The results indicate that in the presence of exogenous fe³⁺ or SO ₄ ²⁺ , methanogenic bacteria were outcompeted for H₂ by bacteria reducing Fe³⁺ or SO ₄ ²⁺ .Deceased on 27 December 1992     

淹水后可变电荷土壤铁锰形态的转化

Ectomycorrhizal fungus Laccaria bicolor S238N,isolated from a forest soil in central France in 1990s,has demonstrated unequivocally and ability to promote pine growth.In the present nursery bed experiment,the ability of this ectomycorrhizal fungus to increase growth and P and K uptake of Douglas Fir seedlings (Zone 22) was examined.Growth of inoculated seedlings was over twice(plant height) and three times (biomass)that of non-inoculated ones.Similarly,both the concentrations and the amounts of P and K uptake by seedlings were significantly increased by fungal inoculation,indicating the improvement of P and K nutrition in mycorrhizal seedlings.In contrast,Al-P in the soils was decreased obviously by plants,especially by mycorrhizas,suggesting utilization of this soil P pool by plants and more efficient Al-P mobilization by mycorrhizas than by nomycorrhizas.Moreover,K extracted by 1mol/L HCl following consecutive extraction of H2O and CH3COONH4,which may not be plant available,could be utilized by fungus colonied roots.This could be explained by the release of protons and oxalate by hypae which leads to replacement of interlayer K in nonexpanded 2:1 clay minerals and bio-weathering of phyllosilicates.