Pump‐and‐Treat Groundwater Remediation Using Chlorine/Ultraviolet Advanced Oxidation Processes

Comparative studies of the use of chlorine/ultraviolet (Cl₂/UV) and hydrogen peroxide/ultraviolet (H₂O₂/UV) Advanced oxidation processes (AOPs) to remove trichloroethylene (TCE) from groundwater in a pump‐and‐treat application were conducted for the first time at the full‐scale operational level at two water treatment facilities in Northern California. In these studies, aqueous chlorine replaced hydrogen peroxide in the AOP treatment step, where the oxidant is exposed to UV light to produce highly reactive radical species that degrade groundwater contaminants. TCE removal rates as a function of initial chlorine dose and pH were then determined. At the site where the natural pH of the water was 7.1, TCE was removed (to a concentration of less than 0.5 µg/L) for nearly every chlorine dose point tested, and pH adjustment slightly enhanced the treatment process at this facility. The second site had a high natural pH of 7.7, and here, TCE was not completely removed for any chlorine dose up to 5.7 mg/L, although TCE removal did increase when the chlorine dose increased between 0.9 and 3.6 mg/L. Residual TCE remaining in the water post‐Cl₂/UV was readily removed using active carbon filtration, which is part of the overall treatment train at this facility. These studies also verified that Cl₂/UV AOP did not interfere with the photolysis of N‐nitrosodimethylamine or result in an effluent acutely toxic toward Ceriodaphnia dubia. Comparative economic analysis revealed that the chemical costs associated with Cl₂/UV AOP were 25 to 50% of the costs associated with in place H₂O₂/UV AOP treatment.     

Trends and Variability in Total Ozone from a Mid-Latitude Southern Hemisphere Site: The Melbourne Dobson Record 1978–2012

Abstract

The Australian Bureau of Meteorology maintains a number of long-running Dobson measurement programs, among the few in southern hemisphere mid-latitudes. Data from the Melbourne site (the Melbourne/Airport World Ozone and Ultraviolet Radiation Data Centre (WOUDC) station was originally located at Aspendale, then moved to the city centre, and finally to Melbourne Airport) from 1978 to 2012 have recently been reviewed and re-evaluated. These data are analyzed using multi-linear regression and also by application of an 11-year running mean. Satellite data from the Merged Ozone Dataset are also used for comparison with the Dobson results. We show that the Quasi-Biennial Oscillation (QBO) plays a major role in winter and spring once phase is taken into account by month. We also show that the three so-called “classical” proxies (QBO, solar cycle, and Equivalent Effective Stratospheric Chlorine (EESC)) alone are able to give a good fit to ozone for Melbourne and, more generally, the southern mid-latitudes for most months of the year, in contrast with the case in the northern hemisphere where dynamical variation plays a much more important role. Correspondingly, the smoothed Melbourne Dobson time series shows a high correlation to EESC.     

东秦岭石窑沟斑岩钼矿床地质特征及辉钼矿Re-Os年龄

在东秦岭钼成矿带最近探明的石窑沟大型钼矿床位于近东西向马超营断裂带与北东向石窑沟-焦园断裂带的交汇部位,获得钼金属储量10余万吨,平均品位0.068%。钼矿化呈细脉-网脉状分布于花岗斑岩体及其围岩熊耳群火山岩中,与矿化有关的围岩蚀变有钾长石化、硅化、绢云母化、黄铁矿化等,具有斑岩型钼矿床的一些基本特点。在矿床中选取5件不同矿化类型的辉钼矿样品,采用ICP-MS法进行Re-Os同位素定年,获得模式年龄131.3±2.4～134.3±2.6Ma,等时线年龄135.2±1.8Ma(MSWD=0.18),形成于早白垩世,与豫西熊耳山地区雷门沟、鱼池岭等钼矿床形成时代相近。据辉钼矿Re含量(8.242×10-6～30.24×10-6)推测,矿床成矿物质主要来自于下地壳。矿床为东秦岭-大别山地区中生代第三期钼成矿作用产物,形成于早白垩世中国东部岩石圈伸展环境。     

Rates of peat accumulation over the past 200 years in fiveSphagnum-dominated peatlands in the United States

Using²¹⁰Pb-dating of peat cores, corroborated by pollen and acid-insoluble ash approaches, rates of vertical height growth, dry mass accumulation, and organic matter accumulation were determined for fiveSphagnum-dominated peatland sites (one in Minnesota, one in Pennsylvania, one on the Maryland/West Virginia border, two in West Virginia), spanning a mean annual temperature range of 4.5 °C and differing in total annual precipitation by a factor of almost 2. Site differences in rates of vertical height growth and dry mass accumulation were documented, but both within-core and between-site differences in bulk density and ash concentrations of peat confound efforts to relate vertical height growth and dry mass accumulation to net organic matter accumulation. Taking bulk densities and ash concentrations into account, rates of net organic matter accumulation over the past 150–200 years were strikingly similar at four of the five sites, an unexpected result given the general trend that with decreasing latitude, peat deposits become older, thinner, and more highly decomposed. More comprehensive studies are needed in which net organic matter accumulation is determined at several locations within a single peatland, at several peatlands within a particular geographic/climatic region, and at peatland sites in different geographic/climatic regions. If additional studies confirm that recent (past 200 years) net organic matter accumulation is relatively insensitive to broad-scale regional climatic differences, boreal and subarctic peatlands may continue to function as a net sink for atmospheric CO₂ and a net source of atmospheric CH₄ with no change in rates of net organic matter accumulation, even under predicted scenarios of global climate change.This publication is the third paper in a series of papers presented at the session on Past Climatic Change and the Development of Peatlands at the ASLO and SWS Meetings in Edmonton, Canada, May 30–June 3, 1993. Dr P. Kuhry and Dr S. C. Zoltai are serving as Guest Editors.     

Stratigraphic Trapping of Spilled Jet Fuel Beneath the Water Table

Environmental conditions and the initial attempt to recover JP-4 jet fuel from a shallow aquifer at a tank farm in Hanahan, South Carolina, in 1975. allowed the jet fuel to become stratigraphically trapped below the water table. The trapped jet fuel remained an undetected source of dissolved hydrocarbon contamination in shallow ground water in the area for 17 years. The trapped jet fuel was located when a variety of chemical, hydrologic. geologic, and historical evidence led investigators to install and sample deeper wells. These findings emphasize the need to use an integrated approach lo evaluating the data when determining the extent of contamination and planning fuel recovery operations in a lithologically heterogeneous aquifer.     

Self-generated aperiodic behaviour in a simple climate model

Climatic variability arising from the coupling between ocean temperature and sea-ice extent is studied in a spatially distributed system. A spatial degree of freedom is crudely introduced by the coupling, through energy transfer, of two box models each of which describes a different space region. The evolution equations are cast into a normal form and some qualitative features of this general class of models are predicted. It is shown, both analytically and numerically, that internally generated complexity in the form of aperiodic behaviour can be a natural consequence of spatially distributed systems.     

Glacial and Fluvial Deposits in the Aragón Valley,Central‐Western Pyrenees: Chronology of the Pyrenean Late Pleistocene Glaciers

The Aragón Valley glacier (Central Western Pyrenees) has been studied since the late nineteenth century and has become one of the best areas in the Pyrenees to study the occurrence of Pleistocene glaciations and the relationships between moraines and fluvial terraces. New morphological studies and absolute ages for moraines and fluvial terraces in the Aragón Valley allow a correlation with other Pyrenean glaciers and provide solid chronologies about the asynchroneity between global last glacial maximum (LGM) and the maximum ice extent (MIE). Six frontal arcs and three lateral morainic ridges were identified in the Villanúa basin terminal glacial complex. The main moraines (M1 and M2) correspond to two glacial stages (oxygen isotopic stages MIS 6 and MIS 4), dated at 171 ± 22 ka and 68 ± 7 ka, respectively. From a topographical point of view, moraine M1 appears to be linked to the 60 m fluvioglacial terrace, dated in a tributary of the Aragón River at 263 ± 21 ka. The difference in age between M1 moraine and the 60 m fluvioglacial terrace suggests that the latter belongs to an earlier glacial stage (MIS 8). Moraine M2 was clearly linked to the fluvioglacial 20 m terrace. Other minor internal moraines were related to the 7–8 m terrace. The dates obtained for the last glacial cycle (20–18 ka) are similar to other chronologies for Mediterranean mountains, and confirm the occurrence of an early MIE in the Central Pyrenees that does not coincide with the global LGM.