Stable carbon isotope ratios of water-extractable organic carbon affected by application of rice straw and rice straw compost during a long-term rice experiment in Yamagata,Japan

ABSTRACT

Hot-water- and water-extractable organic matter were obtained from soil samples collected from a rice paddy 31 years after the start of a long-term rice experiment in Yamagata, Japan. Specifically, hot-water-extractable organic carbon and nitrogen (HWEOC and HWEON) were obtained by extraction at 80°C for 16 h, and water-extractable organic carbon and nitrogen (WEOC and WEON) were obtained by extraction at room temperature. The soil samples were collected from surface (0–15 cm) and subsurface (15–25 cm) layers of five plots that had been treated with inorganic fertilizers alone or with inorganic fertilizers plus organic matter, as follows: PK, NPK, NPK plus rice straw (RS), NPK plus rice straw compost (CM1), and NPK plus a high dose of rice straw compost (CM3). The soil/water ratio was 1:10 for both extraction temperatures. We found that the organic carbon and total nitrogen contents of the bulk soils were highly correlated with the extractable organic carbon and nitrogen contents regardless of extraction temperature, and the extractable organic carbon and nitrogen contents were higher in the plots that were treated with inorganic fertilizers plus organic matter than in the PK and NPK plots. The HWEOC and WEOC δ¹³C values ranged from ?28.2% to ?26.4% and were similar to the values for the applied rice straw and rice straw compost. There were no correlations between the HWEOC or WEOC δ¹³C values and the amounts of HWEOC or WEOC. The δ¹³C values of the bulk soils ranged from ?25.7% to ?23.2% and were lower for the RS and CM plots than for the PK and NPK plots. These results indicate that HWEOC and WEOC originated mainly from rice plants and the applied organic matter rather than from the indigenous soil organic matter. The significant positive correlations between the amounts of HWEOC and HWEON and the amount of available nitrogen (P < 0.001) imply that extractable organic matter can be used as an index for soil fertility in this long-term experiment. We concluded that the applied organic matter decomposed more rapidly than the indigenous soil organic matter and affected WEOC δ¹³C values and amounts.     

铬污染归宿的同位素原位监测法

铬(Cr)污染的迁移和环境毒性主要取决于其化学形态。在环境中,如果移动性及毒性较大的Cr(Ⅵ)能被还原为移动性及毒性较小的Cr(Ⅲ),并且还原速率大于污染速率,那么对铬污染的自然生态修复治理是可行的。铬在氧化还原过程中,存在着同位素动力学分馏效应,致使同位素比率发生移动,移动的大小和反应进程有关,服从Reyleigh关系方程。因此,利用同位素测定可以确定Cr(Ⅵ)的归宿,用于铬(Cr)污染自然修复的监测。本文就环境铬污染自然生态修复中,应用同位素原位分析法进行监测的基本原理、分析过程及应用的可行性进行了阐述。     

N2O emissions from different cropping systems and from aerated,nitrifying and denitrifying tanks of a municipal waste water treatment plant

Nitrous oxide emissions, nitrate, water-soluble carbon and biological O₂ demand (BOD₅) were quantified in different cropping systems fertilized with varying amounts of nitrogen (clayey loam, October 1991 to May 1992), in an aerated tank (March 1993 to March 1994), and in the nitrification-denitrification unit (March to July 1994) of a municipal waste water treatment plant. In addition, the N₂O present in the soil body at different depths was determined (February to July 1994). N₂O was emitted by all cropping systems (mean releases 0.13–0.35 mg N₂O m^-2 h^-1), and all the units of the domestic waste water treatment plant (aerated tank 0–6.2 mg N₂O m^-2 h^-1, nitrification tank 0–204,3 mg N₂O m^-2, h^-1, denitrifying unit 0–2.2 mg N₂O m^-2 h^-1). During the N₂O-sampling periods estimated amounts of 0.9, 1.5, 2.4 and 1.4 kg N₂O–N ha^-1, respectively, were released by the cropping systems. The aerated, nitrifying and denitrifying tanks of the municipal waste water treatment plant released mean amounts of 9.1, 71.6 and 1.8 g N₂O–N m^-2, respectively, during the sampling periods.The N₂O emission were significantly positively correlated with nitrate concentrations in the field plots which received no N fertilizer and with the nitrogen content of the aerated sludge tank that received almost exclusively N in the form of NH ₄ ⁺ . Available carbon, in contrast, was significantly negatively correlated with the N₂O emitted in the soil fertilized with 80 kg N ha^-1 year. The significant negative correlation between the emitted N₂O and the carbon to nitrate ratio indicates that the lower the carbon to nitrate ratio the higher the amount of N₂O released. Increasing N₂O emissions seem to occur at electron donorto-acceptor ratios (C_H2_O or BOD₅-to-nitrate ratios) below 50 in the cropping systems and below 1200–1400 in the waste water treatment plant. The trapped N₂O in the soil body down to a depth of 90 cm demonstrates that agricultural production systems seem to contain a considerable pool of N₂O which may be reduced to N₂ on its way to the atmosphere, which may be transported to other environments or which may be released at sometime in the future.Dedicated to Professor J.C.G. Ottow on the occasion of his 60th birthday     

Direct contribution by soil arthropods to nutrient availability through body and faecal nutrient content

Summary The direct contribution made by soil arthropods to nutrient dynamics was investigated in pine forests that differed in soil nutrient status. Nutrient concentrations (K⁺, Ca²⁺, Mg²⁺, PO ₄ ^3– , N, C) in the most abundant species and groups of arthropods in two Pinus nigra forests were compared, and distinct differences were found among taxonomic groups. In the rank order: collembolans, oribatides, isopods, diplopods, Ca²⁺ and Mg²⁺ concentrations increased, while N and C concentrations decreased. The nutrient concentrations in individuals of the same species but originating from the different forests were similar, except for the isopod Philoscia muscorum. The total and available nutrient concentrations in food and faeces of the collembolan Tomocerus minor and the isopod Philoscia muscorum were compared. The isopod faeces contained relatively less K⁺ and Mg²⁺, and more Ca²⁺, PO ₄ ^3– , and greater N availability, compared with the food material. The collembolan faeces showed a higher availability of all nutrients measured. The N species appeared to be changed by collembolans; their faeces contained high NO ₃ ^– concentrations, while their food contained relatively high concentrations of NH ₄ ⁺ . These findings were examined in relation to their significance for ecosystem functioning. It was concluded that about 12% of the total K⁺, PO ₄ ^3– , N and 2% of the Ca²⁺ in the organic layer was found in the mesofauna. It was calculated that faeces production by the collembolans resulted in a 2.4 times higher NO ₃ ^– availability in the forest floor.     

The use of a water budget model and yield maps to characterize water availability in a landscape

Crop yield maps may contain substantial corollary information regarding the distribution of yield related soil properties across a landscape. One of these properties is water holding capacity (WHC). Since WHC is an important parameter for crop models and is also critical for crop yield, our objective was to determine if WHC could be estimated by matching simulated yield with yield map data. We collected soil cores for water retention measurements and recorded plant phenological stages from 60 plots on four transects over two growing seasons (1997 and 1998). Soil cores were also sampled on 40 other locations set out on a grid pattern. We utilized a simple water budget model that uses the relative transpiration ratio to calculate relative yield from available water in the soil profile. Rainfall, potential evapotranspiration and soil water holding capacity are input. An optimization program varies the WHC to produce a grain yield similar to the one from the yield map at a particular location. This analysis was carried out over several scales by averaging yields over 55 m×71 m, 27 m×35 m, and 11 m×14 m areas. Yield data from 2 years were used. Yields from the transects in both years were significantly related to measured WHC in the surface 0–10 cm of soil. The calculated stress indices from the water budget model and estimated available WHC calculated for the 1997 data were similar to those calculated for the 1998 data where data were aggregated in 27 by 35 m or larger blocks. The contour map of estimated WHC was similar to the map of measured WHC for some features though there were also some differences. Use of multiple years of yield data are required to give stable results for estimated water holding capacities.. This information could be used in a farm management plan by allowing a producer to classify a field into areas that are buffered against drought and areas more susceptible to drought.     

土壤悬浮液中溶解和吸附性铁离子对硫化物还原Cr(VI)的催化作用

The kinetics of Cr(Ⅵ) reduction by sulfide in soil suspensions with various pHs, soil compositions, and Fe(Ⅱ) concentrations was examined using batch anaerobic experimental systems at constant temperature. The results showed that the reaction rate of Cr(Ⅵ) reduction was in the order of red soil < yellow-brown soil < chernozem and was proportional to the concentration of HCl-extractable iron in the soils. Dissolved and adsorbed iron in soil suspensions played an important role in accelerating Cr(Ⅵ) reduction. The reaction involved in the Cr(Ⅵ) reduction by Fe(Ⅱ) to produce Fe(Ⅲ), which was reduced to Fe(Ⅱ) again by sulfide, could represent the catalytic pathway until about 70% of the initially present Cr(Ⅵ) was reduced. The catalysis occurred because the one-step reduction of Cr(Ⅵ) by sulfide was slower than the two-step process consisting of rapid Cr(Ⅵ) reduction by Fe(Ⅱ) followed by Fe(Ⅲ) reduction by sulfide. In essence, Fe(Ⅱ)/Fe(Ⅲ) species shuttle electrons from sulfide to Cr(Ⅵ), facilitating the reaction. The effect of iron, however, could be completely blocked by adding a strong Fe(Ⅱ)-complexing ligand, 1,10-phenanthroline, to the soil suspensions. In all the experiments, initial sulfide concentration was much higher than initial Cr(Ⅵ) concentration. The plots of lnc[Cr(Ⅵ)] versus reaction time were linear up to approximately 70% of Cr(Ⅵ) reduction, suggesting a first-order reaction kinetics with respect to Cr(Ⅵ). Elemental sulfur, the product of sulfide oxidation, was found to accelerate Cr(Ⅵ) reduction at a later stage of the reaction, resulting in deⅥation from linearity for the lnc[Cr(Ⅵ)] versus time plots.     

The contribution of rock fragments to the available water content of stony soils: Proposition of new pedotransfer functions

The contribution of rock fragments to the soil available water content (SAWC) of stony soil has been quantified by measurements of bulk density and gravimetric water content at different water potentials on rock fragments of different lithologies: flints, cherts, chalks, gaizes and limestones. More than 1000 pebbles (2 cm < equivalent diameter of the rock fragment < 5 cm) have been sampled in stony soils developed from each of the five lithologies. We demonstrated that the water content at saturation of the studied pebbles was equal to the water content at −100 hPa and to the water content at field capacity. A linear relationship between the water content at −100 hPa and at −15,840 hPa enabled to derive a simple pedotransfer function to determine the available water content of the rock fragments. We also proposed a second simple pedotransfer function, which expresses the available water content from the dry bulk density of the rock fragments only. A simulation at the horizon scale for a loamy-clay stony horizon showed that the SAWC could be strongly misjudged when the rock fragments were not taken into account: for a stony horizon containing 30% of pebbles, the SAWC is underestimated by 5% for chert pebbles and by 33% for chalk pebbles.     

太阳能热动力系统效率分析

通过对太阳能热动力系统"有效能"效率分析和讨论,提出了提高太阳能热动力系统效率的途径。     

Excess trace metal effects on cotton: 4. Chromium and lithium in Yolo loam soil

Abstract

Two cultivars of cotton (Gossypium spp) were grown in Yolo loam soil in a glasshouse to determine phytotoxicity effects of Cr and Li and possible interactions with other metals. The Cr at 100 μg/g soil had no adverse effects on either cultivar studied. A Cr increase was not observed in either stems or leaves. Both cultivars tolerated 25 and 50 μg Li/g soil. The 50 μg Li/g soil resulted in leaves of Acala SJ‐2 with 432 μg Li/g leaves and 720 in Giza 45. The 100 μg Li/g soil resulted in 74% and 87% leaf yield reductions in Acala SJ‐2 and Giza 45 respectively. Leaf concentrations of Li respectively were 1950 and 1850 μg/g. Except at the highest level of Li, leaves had higher concentrations of Li than did roots. The Cr and Li resulted in some plant metal interactions.