Are Recent Watershed Disturbances Associated with Temporal and Spatial Changes in Water Quality of Lake George, New York, USA?

a (Chl a), silica (Si), and chloride (Cl) through the use of proper statistical techniques. Results indicate no statistically significant changes in the concentrations of TP, Chl a, or Si in the spring or summer from 1981 to 1993. A significant temporal trend of increase in Cl concentration is, however, detected. This is perhaps the strongest evidence that the development of the Lake George watershed has affected lakewater chemistry. In spring, the concentrations of TP, Chl a, Si, and Cl, averaged over all 13 years, were higher in the south basin, but differences are not statistically significant (i.e., P > 0.05). In summer, Si was slightly but significantly lower, and Cl was nonsignificantly higher in the south basin. Significant interactions between temporal and spatial changes are detected based only on summer values of TP and Chl a, indicating differential trends of change for these two variables in the south and north basins during the last 13 years.     

TRENDS IN PRECIPITATION AND STREAM CHEMISTRY IN A PRISTINE OLD-GROWTH FOREST WATERSHED,OLYMPIC NATIONAL PARK,WASHINGTON1

ABSTRACT: Human induced long-term changes in precipitation and stream chemistry have been observed in eastern North America and Europe, but few long-term studies have been conducted in coastal western North America. The objectives of this research were to determine: (1) time trends in precipitation and stream chemistry in a pristine old-growth forest watershed, and (2) seasonal patterns in precipitation and stream chemistry. It was conducted in 58 ha West Twin Creek Watershed, Hoh River Valley, Olympic National Park, Washington from 1984 to 1993. Vegetation consists of old-growth forest, with western hemlock, Douglas-fir, western redcedar, Pacific silver fir, and Sitka spruce being the dominant tree species. Annual precipitation varied from 2336 to 4518 mm during the study period with the majority of the rain falling between October and May. Chemistry of precipitation was strongly dominated by oceanic influences with Na and Cl being the dominant ions. The chemistry of the stream was influenced by bedrock weathering and was dominated by Ca, HCO₃, and SO₄ and was not strongly related to precipitation chemistry. The pH of precipitation averaged 5.3 over time and ranged from 4.3 to 7.1, while the stream pH averaged 7.5 and ranged from 5.5 to 9.0. There were few long-term trends in the chemical constituents of bulk precipitation or stream water with the exception of a slight decrease in NO₃ in precipitation and an increase of SO₄ in stream water. A trend of decreasing concentrations of Ca, Mg and Na in precipitation also occurred. There were no significant seasonal patterns in precipitation although the highest SO₄ concentrations usually occurred in late spring and summer perhaps due marine algal activity. Strong seasonal trends occurred in concentrations of HCO₃, SO₄, Ca, Mg, and Na in stream water resulting from weathering and stream flow patterns, with highest ion concentrations occurring just before the onset of the rainy season. Pulses of NO₃ in the stream were observed during fall and early winter resulting from the release of NO₃ which had accumulated in soils or sediments.     

还原法处理电镀废水后铬反弹成因分析与对策

从化学热力学和电化学理论出发，结合目前普遍采用的还原——固体分离法处理含铬废水工艺，对固液分离后的上清液和沉降污泥Cr^6 含量以及Cr^3 ～Cr^6 之间的形态转化相关性进行研究和分析，进而提醒人们要特别注意控制含铬污水中铬反弹及全过程处理的完整性。     

Application of ground-based Lidar for studies of the dynamics of ozone in a mountainous basin

A ground-based Differential Absorption Lidar was employed to study the dynamics of atmospheric O3 within the planetary boundary layer of a basin in the 'Fichtelgebirge' mountains, NE Bavaria. In particular, the night-time dynamics of O3 linked to the ground were investigated. The Lidar system measured vertical profiles of O3 up to 1 km above ground. For detailed analysis of the night-time dynamics of ozone, supplementary data from three ground-based stations (measuring mixing ratios of O3 and NO(x), as well as meteorological parameters) are essential. The Lidar results could be evaluated with these data from various altitudes above the basin floor. For the station with the largest (vertical) distance to the ground-based Lidar, the agreement was very good at all times. The Lidar method proved to be useful for examining the spatial distribution of O3. The observed night-time decrease of O3 at the bottom of the basin was due to deposition and to advection of air masses containing less O3 from the mountain slopes.     

Characterization of precipitation in the background of atmospheric pollutants reduction in Guilin: Temporal variation and source apportionment

Rainfall samples were collected from three observation sites in Guilin from 2013 to 2017, and the chemical composition characteristics of precipitation and the contribution made by different ion sources were analyzed when atmospheric pollutants levels were reduced. The results showed that acid gas emissions and atmospheric pollutant concentrations continued to decline during the study period. However, the change in the volume-weighted mean pH at the three sites suggested that acid rain pollution was not alleviated and began to deteriorate after 2015. The continuing downward trend for alkaline neutralizing ions (Ca²⁺, NH₄⁺) in precipitation indicated that the reduction in alkaline neutralizing substances in the atmosphere was an important factor that led to the deterioration in acid rain across Guilin. The principal component analysis and spearman correlation analysis indicated five sources of ions in precipitation. Quantitative assessment of these five sources indicated that fossil fuel combustion contributed the most ions concentration in precipitation at the three sites, followed by agriculture, terrestrial (crustal) sources, marine sources, and biomass burning. Long-distance airflow might affect the acidity, the electrical conductivity (EC), and ion concentrations in precipitation across Guilin. The airflow trajectory from the west and southeast directions corresponded to higher acidity and ion concentrations. According to the current air pollution control strategy planned by Guilin, reducing atmospheric coarse particles and NH₃ at the same time may potentially lead to further deteriorations in acid rain contents. Therefore, Guilin needs to develop more reasonable pollution prevention measures that synergistically control atmospheric pollutants and acid rain pollution.     

Long-Term and Seasonal Changes in Chemical Composition of Surface Waters in Latvia

The changes of the chemical composition in Latvianinland waters over the last twenty years weredetermined, based on data of the National MonitoringProgramme. Relationships between the water compositionwere studied. The chemical composition and seasonalchange pattern depend a lot on hydrological factorswhich differed between eastern and western Latvia.Different pattern of long-term changes is found forsubstances which have different sources andsinks, at first for nutrients (decrease only in the lastfew years) and inorganic ingredients (commonlyincreasing trend). An attempt was made to identify themain sources of the major water ingredients and linkchanges of their concentrations with changes inloading to waters.     

Developing a National Indicator of Soil Quality on U.S Forestlands: Methods and Initial Results

The Montreal Process was formed in 1994 to develop an internationally agreed upon set of criteria and indicators for the conservation and sustainable management of temperate and boreal forests. In response to this initiative, the Forest Inventory and Analysis (FIA) and Forest Health Monitoring (FHM) programs of the United States Department of Agriculture Forest Service have implemented soil measurements as part of a national monitoring program to address specific questions related to the conservation of soil and water resources. Integration of soil assessments into the national FIA program provides for systematic monitoring of soil properties across all forested regions of the U.S. using standardized collection, laboratory, and statistical procedures that are compatible with existing forest inventory data. The resulting information will provide quantitative benchmarks for regional, national, and international reporting on sustainable forest management and enhance our understanding of management effects on soil quality. This paper presents an overview of the FIA soil monitoring program, outlines the field and laboratory protocols as currently implemented, and provides examples of how these data may be used to assess indicators of sustainable management as defined by the Montreal Process.     

CHANGES IN ACID PRECIPITATION-RELATED WATER CHEMISTRY OF LAKES FROM SOUTHWESTERN NEW BRUNSWICK, CANADA, 1986–2001

Between 1986 and 2001, thirty-nine lakes in southwestern New Brunswick in Atlantic Canada were surveyed for acid precipitation-related water quality changes. Most of the study lakes are located on granite bedrock and represent the most acid sensitive lakes in the province. Between 1987 and 1992, hydrogen ion deposition to the lake study area averaged 452 eq ha^–1 yr^–1, compared to 338 eq ha^–1 yr^–1 between 1993 and 2000, a 25% reduction. The lake chemistry data were evaluated by dividing the lakes into four clusters for each survey year based on their acid neutralizing capacity. Twenty percent of the lakes (cluster IV) had an average ANC of 40 eq L^–1or greater and maintained an average pH of greater than 6 over the duration of the study period. A pH of 6 or greater is considered a healthy benchmark for maintaining biodiversity. The remaining 31 lakes (clusters I to III) had an average ANC of less than 40 eq L^–1and maintained an average pH of less than 6. Other lake chemistry changes included a general decline in lake sulphate and colour over the duration of the survey period, followed by more recent improvements in calcium ion, pH and ANC, and notably higher but declining aluminum levels in lower ANC and pH lakes. Nitrate accounted for 37% of the acid deposition to the study area, however it was not detectable in the lakes. Although acid deposition has declined and these lakes are beginning to show signs of acid recovery, 80% of the study lakes remain acid sensitive having little buffering capacity with low calcium, pH and ANC.     

Green Chemistry - Views and Strategies * (5 pp)

Background and Goal The object of Green Chemistry is the reduction of chemical pollutants flowing to the environment. The Chemistry and the Environment Division of EuCheMS has assumed Green Chemistry as one of its areas of interest, but one question to solve is where Green Chemistry should be placed within the context of Chemistry and the Environment. The concept of Green Chemistry, as primarily conceived by Paul Anastas and John Warner, is commonly presented through the Twelve Principles of Green Chemistry. However, these Twelve Principles, though fruit of a great intuition and common sense, do not provide a clear connection between aims, concepts, and related research areas of Green Chemistry. These two unsolved questions are the object of the present article.Discussion Green Chemistry is here placed as a part of Chemistry for the Environment, concerning the still non-existent pollutants. Indeed, the object of Green Chemistry is the reduction of pollution and risks by chemicals by avoiding their generation or their introduction into the biosphere. The distinction between pollutant chemicals and dangerous chemicals, along with the consideration of the exhaustion of fossil resources and the acknowledgement of the harmful effects of the chemicals employed in a great variety of activities, leads to the recognition of four general objectives for Green Chemistry. In order to accomplish these general objectives, a number of strategies, or secondary objectives and some fundamental concepts, namely, atomic economy, selectivity, potential harm or historical harm can be visualized. A connection is finally established between the strategies and current and future research areas of Green Chemistry.Conclusion The ultimate aim of green chemistry is to entirely cut down the stream of chemicals pouring into the environment. This aim seems unattainable at present, but progress in the green chemical research areas and their application through successive approaches will certainly provide safer specialty chemicals and much more satisfactory processes for the chemical industry.- * The basis of this peer-reviewed paper is a presentation at the 9th FECS Conference on ‘Chemistry and Environment’, 29 August to 1 September 2004, Bordeaux, France.     

Life Cycle Assessment as Part of Sustainability Assessment for Chemicals (5 pp)

Background LCA is the only internationally standardized environmental assessment tool (ISO 14040-43) for product systems, including services and processes. The analysis is done ‘from cradle-to-grave’, i.e. over the whole life cycle. LCA is essentially a comparative method: different systems fulfilling the same function (serving the same purpose) are compared on the basis of a ‘functional unit’ - a quantitative measure of this function or purpose. It is often believed that LCA can be used for judging the (relative) sustainability of product systems. This is only partly true, however, since LCA is restricted to the environmental part of the triad ‘environment/ecology - economy - social aspects (including intergenerational fairness)’ which constitutes sustainability. Standardized assessment tools for the second and the third part are still lacking, but Life Cycle Costing (LCC) seems to be a promising candidate for the economic part. Social Life Cycle Assessment still has to be developed on the basis of known social indicators.Method and Limitations LCA is most frequently used for the comparative assessment or optimization analysis of final products. Materials and chemicals are difficult to analyse from cradle-to-grave, since they are used in many, often innumerable product systems, which all would have to be studied in detail to give a complete LCA of a particular material or substance! This complete analysis of a material or chemical is evidently only possible in such cases where one main application exists. But even if one main application does exist, e.g. in the case of surfactants (chemicals) and detergents (final products), the latter may exist in a great abundance of compositions. Therefore, chemicals and materials are better analysed ‘from cradle-to-factory gate’, leaving the analysis of the final product(s), the use phase and the ‘end-of-life’ phases to specific, full LCAs.Conclusion A comparative assessment of production processes is possible, if the chemicals (the same is true for materials) produced by different methods have exactly the same properties. In this case, the downstream phases may be considered as a ‘black box’ and left out of the assessment. Such truncated LCAs can be used for environmental comparisons, but less so for the (environmental) optimization analysis of a specific chemical: the phases considered as ‘black box’ and left out may actually be the dominant ones. A sustainability assessment should be performed at the product level and contain the results of LCC and social assessments. Equal and consistent system boundaries will have to be used for these life cycle tools which only together can fulfil the aim of assessing the sustainability of product systems.