An expert system for water quality modelling

The RAISON-micro (Regional Analysis by Intelligent System ON a micro-computer) expert system is being used to predict the effects of mine effluents on receiving waters in Ontario. The potential of this system to assist regulatory agencies and mining industries to define more acceptable effluent limits was shown in an initial study. This system has been further developed so that the expert system helps the model user choose the most appropriate model for a particular application from a hierarchy of models. The system currently contains seven models which range from steady state to time dependent models, for both conservative and nonconservative substances in rivers and lakes. The menu driven expert system prompts the model user for information such as the nature of the receiving water system, the type of effluent being considered, and the range of background data available for use as input to the models. The system can also be used to determine the nature of the environmental conditions at the site which are not available in the textual information database, such as the components of river flow. Applications of the water quality expert system are presented for representative mine sites in the Timmins area of Ontario.     

The predicted effect of SO2 emission controls on the water quality of eastern Canadian lakes

Changes in SO _inf4 ^sup2- deposition predicted to occur in response to implementation of announced SO₂ emission control programs in Canada and the U.S.A. have been used as input to water chemistry models thereby giving an estimate of the changes in lake acid neutralizing capacity (ANC) and pH that can be expected from these programs. Eastern Canada has been divided into 22 subregions for the purpose of this analysis. Relative to the current level (1982–86) of SO _inf4 ^sup2- deposition (Scenario 1), the effect of the Canadian SO₂ emission control program alone (Scenario 2) is compared to that obtained when controls are implemented throughout North America (Scenarios 3 and 4). SO₂ emission reduction will effect a shrinkage of the high wet SO _inf4 ^sup2- deposition field in NE North America such that under Scenario 4 conditions, almost no area will remain in Canada that receives >20 kg ha^-1 yr^-1. The greatest decrease in deposition and resulting change in lake chemistry occurs in southern Ontario and southwestern Quebec. ANC distributions shift to higher concentrations and the percentage of lakes having pH<6 decreases in these areas. The Atlantic Provinces will obtain only a minor benefit from the control programs, i.e. experiencing only a small decrease in deposition and improvement in water quality. High sensitivity of the terrain in many parts of Atlantic Canada means that large numbers of lakes will remain acidic (i.e. ANC<0) and/or have pH<6 (an important biological threshold) even after full implementation of the current plans for SO₂ control in Canada and the U.S.     

The effect of oxygen addition on the determination of cadmium and lead in blood and foods by graphite furnace atomic absorption spectrometry

It is well known that in the analysis of low temperature vaporized metal elements such as cadmium and lead, a high ashing temperature causes a loss of the target atoms at the ashing stage, while low ashing temperature causes incomplete decomposition of organic components in the sample. In order to solve these problems, the effect of oxygen addition on determination of cadmium and lead in blood and foods was studied. Oxygen was introduced into the atmosphere in the graphite furnace at the beginning of ashing stage for 20 seconds at 0.5 l/min. Relation between ashing temperature and sensitivity was examined, and the oxygen addition minimized signal depression by the sample matrix. It can be concluded that the addition of oxygen at the ashing stage not only reduces the background absorption, but also suppress the volatilization of target atoms at the ashing stage by the formation of their oxides.     

Dissolved organic iodine in marine waters: role in the estuarine geochemistry of iodine

Non-volatile dissolved organic iodine (DOI) can be a major, or even the dominant, species of dissolved I in coastal, inshore and estuarine waters. It can be converted to IO3- in the presence of an oxidizing agent and to I- by reacting it with a reducing agent. Depending on the exact experimental conditions, the yields of these reactions may not be quantitative. In previous analytical schemes for the determination of IO3-, I- and DOI in marine waters, if oxidation or reduction steps are involved and the concentrations of one or more species are estimated by difference, the presence of DOI can lead to an overestimation of the concentrations of the inorganic species determined by difference and an underestimation of the concentration of DOI. In two cruises covering the James River to the southern Chesapeake Bay and from the southern Chesapeake Bay to the Atlantic, above a salinity (S) of 2, the contribution of DOI to total I increased with decreasing salinity and reached a maximum of 80%. DOI, I- and IO3- were successively the dominant form of dissolved I at 0.1 < S < 15 in the James River estuary, 15 < S < 30 in the Southern Chesapeake Bay and S > 30 in the Atlantic Ocean at the Bay mouth, respectively. Total I behaved conservatively (i.e., no evidence of consumption or production) during estuarine mixing during both cruises. In the southern Chesapeake Bay, total inorganic I was also approximately conservative. The primary process affecting the speciation of dissolved I was the conversion of IO3- to I-. In the James River estuary, there were indications of the conversion of both IO3- and I- to DOI. The concentrations of total I, IO3-, I- and DOI in James River water were 0.121, undetectable, 0.068 and 0.053 microM, respectively. These concentrations of total I and I- are significantly higher while that of IO3- is noticeably lower than those used presently for estimating global riverine input of these I species to the oceans. The riverine flux of DOI to the oceans is presently unknown.     

Distribution of polycyclic aromatic hydrocarbons in the atmosphere of Hong Kong

This paper reports the monitoring results of eleven polycyclic aromatic hydrocarbons (PAHs), four to six-ring, at two urban sites-Central & Western (CW) and Tsuen Wan (TW) in Hong Kong from January to December 2000; and the findings of a study conducted in 2001 of the partitioning of the gaseous and particulate phases of PAHs. The sum of the eleven PAHs under study (sigmaPAHs) was found to range from 6.46 to 38.8 ng m(-3). The annual mean levels at 12.2 ng m(-3) and 15.8 ng m(-3) for CW and TW respectively are comparable to those recorded for the previous two years and are also within the reported ranges for other metropolitan cities in the Asia Pacific region. Amongst the selected eleven PAHs, fluoranthene and pyrene were the two most abundant found in the urban atmosphere of Hong Kong during the study period accounting for approximately 80%, of the total PAHs. The ratios of benzo(a)pyrene to benzo(g,h,i)perylene (BaP/BghiP) and indeno(1,2,3-cd)pyrene to benzo(g,h,i)perylene (IDP/BghiP) indicate that diesel and gasoline vehicular exhausts were the predominant local emission sources of PAHs. Seasonal variations with high winter to summer ratios for each of the individual PAHs (CW: 1.6-16.7 and TW: 0.82-8.2) and for sigmaPAHs (CW: 1.9 and TW: 1.8) and a spatial variation of BaP amongst the air monitoring stations are noted. Results of correlation studies illustrate that local meteorological conditions such as ambient temperature, solar radiation, wind speed and wind direction have significant impact on the concentrations of atmospheric PAHs accounting for the observed seasonal variations. A snapshot comparison of the concentrations of PAHs at four sites including a roadside site, a rural site and the two regular urban sites CW and TW was also performed using the profiles of PAHs recorded on two particulate episode days in March 2000.     

Sludge-grown algae for culturing aquatic organisms: Part I. Algal growth in sludge extracts

This project is aimed at studying the feasibility of using sewage sludge to prepare culture media for microalgae (Chlorella-HKBU) and the use of the sludge-grown algae as a feed for some aquatic organisms. Part I of the project included results on preparing sludge extracts and their use on algal culture. By comparing two culturing techniques, aeration and shaking, it was noted that both lag and log phases were shortened in the aeration system. A subsequent experiment noted that algal growth subject to aeration rates of 1.0 and 1.5 liters/min had similar lag and log phases. In addition, both aeration rates had a significantly higher (P < 0.05) final cell density than that of 0.5 liters/min. A detailed study on the variation of growth conditions on the algal growth was done. The results indicated that pH values of all the cultures declined below 5 at day 12. The removal rates of ammonia N ranged from 62% to 70%. The sludge-grown algae contained a rather substantial amount of heavy metals (µg/g): Zn 289–581, Cu 443–682, Ni 310–963, Mn 96–126, Cr 25–118, and Fe 438–653. This implied that the rather high levels of heavy metals may impose adverse effects on higher trophic organisms.     

Soil and plant characteristics of landfill sites near Merseyside,England

An ecological survey of the plant and soil characteristics was carried out on three landfill sites near Merseyside, England. It was discovered that bare ground at two of the landfill areas had high levels of methane contained in the soil air (Sefton Meadows landfill: 6–8% at 35 cm and 16–35% at 65 cm below soil surface; Coalgate Lane landfill: 1–24% at 35 cm and 39–45% at 40 cm below soils surface), causing the appearance of dark grey reduced regions in the soil, a phenomenon similar to flooded soil. The wellvegetated areas at the two sites had lower levels of methane (under 7%).In areas relatively free of methane, the concentrations of mineralized N and NO₃ ^– had significant correlations with the dry weights of vegetation (r = 0.71 withp<0.01;r=0.61 withp<0.02 accordingly), indicating the necessity of applying available nitrogen fertilizer.     

Acid-forming capacity of lead–zinc mine tailings and its implications for mine rehabilitation

Acid mine drainage problems were experienced in a Pb–Zn mine operation at Lechang, in the northern part of Guangdong Province, People's Republic of China. Geochemical and acid generation evaluations were made on fresh tailings including tailings fine, tailings sand and high sulphide tailings, and oxidised tailings with the aim of providing information on mine rehabilitation. All fresh tailings had a pH higher than 7 while the oxidised tailings had a pH of 4.9 (range 1.6 to 7.4). Only samples with pH < 3 had an electrical conductivity (EC) > 4 dS m-1. Total S contents of all tailings samples were very high with the high sulphide fraction having a mean S content of 38%. All fresh tailings had a high acid neutralisation capacity (ANC) while half of the oxidised tailings had an ANC less than zero. The results from the acid–base account and the net acid generation test indicated that all fresh and oxidised tailings samples were acid-forming except for the sand fraction samples. All tailings samples contained high total concentrations of Cd, Cu, Fe, Pb and Zn but low concentrations of total nitrogen and phosphorus. The preliminary results demonstrated that the tailings were all acid-forming especially the high sulphide fraction which should be kept permanently unexposed under impermeable cap or water.     

阳离子改性粘土对活性染料的脱色作用

金属离子改性的凹凸棒石和膨润土对水中活性艳红染料Ｋ－２ＢＰ的吸附脱色作用符合Ｆｒｅｕｎｄｌｉｃｈ吸附等温式并呈现一级反应动力学的特征，吸附的最佳ＰＨ范围分别为〈５和〈６，其中以改性凹凸棒石的吸附性能较好，光照检验表明，改性膨润土还具有一定的光化学催化降解作用。     

Environmental factors affecting growth of grasses,herbs and woody plants on a sanitary landfill

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