Estimating Forest Ecosystem Evapotranspiration at Multiple Temporal Scales With a Dimension Analysis Approach1

Abstract:  It is critical that evapotranspiration (ET) be quantified accurately so that scientists can evaluate the effects of land management and global change on water availability, streamflow, nutrient and sediment loading, and ecosystem productivity in watersheds. The objective of this study was to derive a new semi‐empirical ET modeled using a dimension analysis method that could be used to estimate forest ET effectively at multiple temporal scales. The model developed describes ET as a function of water availability for evaporation and transpiration, potential ET demand, air humidity, and land surface characteristics. The model was tested with long‐term hydrometeorological data from five research sites with distinct forest hydrology in the United States and China. Averaged simulation error for daily ET was within 0.5 mm/day. The annual ET at each of the five study sites were within 7% of measured values. Results suggest that the model can accurately capture the temporal dynamics of ET in forest ecosystems at daily, monthly, and annual scales. The model is climate‐driven and is sensitive to topography and vegetation characteristics and thus has potential to be used to examine the compounding hydrologic responses to land cover and climate changes at multiple temporal scales.     

Comparison of 85Kr and 3H Apparent Ground‐Water Ages for Source Water Vulnerability in the Collyer River Catchment,Maine1

Abstract: Apparent ground‐water ages as determined by the noble gas isotope ⁸⁵Kr and the water isotope ³H are compared. Refined gas extraction methodology at the wellhead permits efficient collection of Kr for ⁸⁵Kr isotope enrichment. ⁸⁵Kr isochrones elucidate areas of much younger ground‐water ages than ³H. Declining ³H activities in the catchment prevent its correlation with the youngest measured ⁸⁵Kr ages. Source water for most drinking water supplies in the Collyer River catchment is recharged within 40 years BP (2004). Mean‐age (τ) transport modeling suggests uncertainty of ground‐water ages is greatest in the central basin area.     

我国水事纠纷解决机制探析

水事纠纷解决机制是一系列水事纠纷解决方式所组成的整体,该机制是民事主体或行政区域水资源权利受到侵害,以及遭受水污染侵权损害的重要救济途径。虽然我国相关法律对水事纠纷的解决方式已作出规定,但是这些法律规定较为分散、不系统,还没有形成一个有机的整体,造成运用该机制解决水事纠纷的效果较差。为了保障水事纠纷及时、有效地得以解决,完善我国的水事纠纷解决机制已迫在眉睫。     

Assessing water quality of drinking water distribution system in the South Taiwan

This investigation conducted a full-scale survey the drinking water distribution system in Kaohsiung city, Taiwan. The aim was to investigate whether the distribution system was capable of maintaining high water quality from the water treatment facilities through to the end user. The results showed that the distribution system can maintain high water quality, except for suitable chlorine residuals. The authors plotted chlorine residual contour maps to identify areas with low chlorine residuals, helping them prioritize sections that must be flushed or renewal. The contour maps also provide sufficient and clear information for locating booster chlorination stations. Contour maps enable water facilities to identify how water quality decays in the distribution systems and the locations of such decay. Water quality decay can be caused by properties of pipeline materials, hydraulic conditions, and/or biofilm thickness. However, understanding the exact reasons is unnecessary because the contour maps provide sufficient information for trouble-shooting the distribution systems.     

底泥中重金属毒性的室内孔隙水分析技术

根据孔隙水中重金属的浓度可以判定底泥中重金属的毒性但获得真正的底泥孔隙水十分困难。本文提供了一套简便易行的室内原状孔隙水取样技术,将碳化硅砂芯埋入底泥,添加表层水并静置９０ｄ,通过渗滤获得孔隙水,测定孔隙水中重的浓度,所得结果与微生态系统暴露试验中生物指示的重金属的毒性大小相吻合,与生物积累重金属的浓度显著正相关。     

生物过滤技术在大气污染控制中的应用

生物过滤是控制大气污染的经济有效技术,具有较好的发展前景。本文介绍了生物过滤技术处理废气的研究,应用历史,现状,和生物过滤理论,分析了工艺的使用范围,设计及运行控制要点,列举了应用的范例。     

亚铵法制浆黑液作肥料对水环境影响的研究

通过亚铵法制浆蒸煮黑液直接作农肥施于水稻田的研究,给出了不同施肥方式连续数天田间水和渗滤水中黑液污染物变化情况,定量描述了黑液作肥料直接施于水稻田对水环境的影响。     

Sulphur transformation and deposition in the rhizosphere of Juncus effusus in a laboratory-scale constructed wetland

Sulphur cycling and its correlation to removal processes under dynamic redox conditions in the rhizosphere of helophytes in treatment wetlands are poorly understood. Therefore, long-term experiments were performed in laboratory-scale constructed wetlands treating artificial domestic wastewater in order to investigate the dynamics of sulphur compounds, the responses of plants and nitrifying microorganisms under carbon surplus conditions, and the generation of methane. For carbon surplus conditions (carbon:sulphate of 2.8:1) sulphate reduction happened but was repressed, in contrast to unplanted filters mentioned in literature. Doubling the carbon load caused stable and efficient sulphate reduction, rising of pH, increasing enrichment of S(2-) and S(0) in pore water, and finally plant death and inhibition of nitrification by sulphide toxicity. The data show a clear correlation of the occurrence of reduced S-species with decreasing C and N removal performance and plant viability in the experimental constructed wetlands.     

Heavy metal contamination in the vicinity of an industrial area near Bucharest

BACKGROUND, AIMS AND SCOPE: Chromium enters into the aquatic environment as a result of effluent discharge from steel works, electroplating, leather tanning industries and chemical industries. As the Cr(VI) is very harmful to living organisms, it should be quickly removed from the environment when it happens to be contaminated. Therefore, the aim of this laboratory research was to develop a rapid, simple and adaptable solvent extraction system to quantitatively remove Cr(VI) from polluted waters. METHODS: Aqueous salt-solutions containing Cr(VI) as CrO4(2-) at ppm level (4-6 ppm) were prepared. Equal volumes (5 ml) of aqueous and organic (2-PrOH) phases were mixed in a 10 ml centrifuge tube for 15 min, centrifuged and separated. Concentrations of Cr(VI), in both the aqueous and organic phases, were determined by atomic absorption spectrometry. The effects of salt and acid concentrations, and phase-contact time on the extraction of Cr(VI) were investigated. In addition, the extraction of Cr(VI) was assessed in the presence of tetramethylammonium chloride (TMAC) in 2-PrOH phase. Effects of some other metals, (Cd(II), Co(II), Cu(II), Ni(II) and Zn(II)), on the extraction of Cr(VI) were also investigated. RESULTS AND DISCUSSION: The Cr(VI) at ppm level was extracted quantitatively by salting-out the homogeneous system of water and 2-propanol(2-PrOH) using chloride salts, namely CaCl2 or NaCl, under acidic chloride media. The extracted chemical species of Cr(VI) was confirmed to be the CrO3Cl-. The ion-pair complex extracted into the organic phase was rationalized as the solvated ion-pair complex of [2-PrOH2+, CrO3Cl-]. The complex was no longer stable. It implied the reaction between extracted species. Studies revealed that salts and acid directly participated in the formation of the above complex. Use of extracting agents (TMAC) didn't show any significant effect on the extraction of Cr(VI) under high salting-out conditions. There is no significant interference effect on the extraction of Cr(VI) by the presence of other metals. The Cr(VI) in the organic phase was back-extracted using an aqueous ammonia solution (1.6 mol dm(-3)) containing 3 mol dm(-3) NaCl. The extraction mechanism of Cr(VI) is also discussed. CONCLUSIONS: Salting-out of homogeneous mixed solvent of 2-propanol can be employed to extract Cr(VI) quantitatively, as an ion-pair of [2-PrOH2+ * CrO3Cl-] solvated by 2-PrOH molecules. Then, the complex becomes 'solvent-like' and is readily separated into the organic phase. The increase of Cl- ion concentration in the aqueous phase favors the extraction. The 2-PrOH, salts and acid play important roles in the extraction process. There is no need to use an extracting agent at a high salting-out condition. RECOMMENDATIONS AND PERSPECTIVES: Chromium(VI) must be quickly removed before it enters into the natural cycle. As the 2-PrOH is water-miscible in any proportion, ion-pairing between 2-PrOH2+ and CrO3Cl- becomes very fast. As a result, Cr(VI) can easily be extracted. Therefore, the method is recommended as a simple, rapid and adaptable method to quickly separate Cr(VI) from aqueous samples.     

液晶显示器液晶处理与铟回收技术

在实验室条件下,对液晶显示器回收的各个重要环节作了初步的探索,提出了一整套回收工艺.其中包括利用丙酮常温浸取去除偏光片、分离玻璃基板、溶解液晶,还包括利用硫酸溶液和二氧化锰联合浸取玻璃基板,铟的浸取率达89%.得到的铟的酸液经过萃取、置换和电解,可以得到铟的产品,为液晶显示器的资源化和无害化提供实验数据和技术支持.