Molmasseverteilung der organischen Stoffe im Prager Trinkwasser

The water supply of Prague is based upon three different water resources: artesian groundwater and infiltrate of the Jizera river, water of the Vltava and Zelivka rivers. The processing techniques are different; consequently for the purpose of increasing capacity one has to search for the suitable raw water quality as well as for the optimum treatment process. An essential parameter for this is the contents of organic substances whose molar mass distribution is investigated by gel chromatography with the aid of Sephadex G-10, G-25 and G-50. With respect to the total load of organic matter the Jizera shows the lowest values, in the Vltava the C.O.D. values are the highest, in the Zelivka the organic carbon shows the highest values. 80% of the organic substances in water have molar masses below 700. By flocculation 60… 70% of the C.O.D.-Cr can be eliminated, the optimum removal of the high-molecular substances occurring at pH = 6 and with 50… 60 g/m³ aluminium sulphate.     

Formation of Humic-like Substances in Mixed and Pure Cultures of Aquatic Microorganisms

A natural decay of plant and animal biomass in aquatic environments results in the release of different simple structured organic substances into water. In our laboratory experiments we investigated whether some of them, e.g., starch or peptone, and also a complex yeast biomass can be transformed into humic-like substances by natural assemblages and some pure cultures of aquatic microorganisms. After a 6 months incubation most of the cultural media enriched with those natural organic substrates turned dark in color and humic-like substances (HS) could be isolated. However, the original substrate organic carbon was mainly mineralized in microbial cultures, and only about 3 % C was converted into HS. Total yields of HS differed in dependence of the individual substrate used (peptone > yeast > starch), the origin of inoculum (river > lake > groundwater), and the incubation temperature (20°C > 10°C). According to their elemental composition, and their spectroscopical and electrophoretic characteristics the microbially formed HS resembled natural aquatic humic matter, but were higher in aliphatic constituents (carbohydrates, peptides) and lower in aromatic structures. HS-like substances were also obtained from pure cultures of a bacterium Bacillus sphaericus and a fungus Cladosporium cladosporioides. The ¹³C and ¹⁵N isotopic contents of the microbially produced HS differed in dependence on the microbial inoculum and the type of organic substrates used, but in general they indicated anabolic processes to be mainly responsible for the humification of the simple organic substrates used in our experiments.     

Surface-active substances on rainwater and atmospheric particles

The surface tension lowering by surface-active substances has been measured on rainwater, melted snow, and dispersions of atmospheric particles in water, with a film balance and a tensiometer. The precipitation water was sampled during 1979, 1980, and 1981 in the city of Frankfurt/Main. From measurements with the film balance technique, normalized concentrations of insoluble and weakly soluble surface-active substances have been estimated. Soluble surface-active substances were determined from measurements with a tensiometer. It was found that the normalized concentration of theinsoluble and weakly soluble surface-active material on rainwater or melted snow shows a maximum during late spring of about 2.5 · 10⁻⁷ moles/l and a minimum during wintertime of about 5 · 10⁻⁸ moles/l. These concentrations are too low to influence significantly the condensation of water vapour on cloud droplets or the evaporation of water from them. Thesoluble surface-active material on rainwater or melted snow was found to have concentrations of the order of 2 · 10⁻⁶ moles/l. These concentrations are also too small to have a significant influence on cloud physical processes.     

Nitrat im Trinkwasser — hygienische und aufbereitungstechnische Probleme

The increasing nitrate concentrations in the ground water and drinking water which are caused by intensified fertilizing lead to the risk of methaemoglobinaemia of babies and increase the cancerogenic, teratogenic and mutagenic risk for the total population. In the drinking water conditioning the nitrate concentration can be reduced by different techniques. By ion exchange first the SO₄-ions and then the nitrate-ions are removed. Very favourable is the exchange for HCO and the regeneration by means of carbon dioxide and CaCO₃, for which a mass balance of substances is given. With 0.55 DM/m³ also the reverse osmosis in a mixture with raw water is practicable and also electrodialysis can be applied, whereas the biological techniques of the heterotrophic or autotrophic denitrification still include unsolved technological problems due to the necessity of an organic substrate or of H₂. The special features of each of these techniques and the hygienic and also the corrosion-chemical consequences are indicated.     

Dissolved Organic Carbon in Seepage Water – Production and Transformation during Soil Passage

Dissolved organic carbon (DOC) in seepage water can combine with organic pollutants, with Al and heavy metal ions and transport them through the soil profile with a potential to contaminate groundwater. We studied the production of DOC in aerobic decomposition experiments at 8 °C and moisture close to field capacity in soils from two sites with different microbial activities (spodic dystric Cambisols with moder (SLB) and mor‐moder (SLS) layers) using ¹³C‐depleted plants of differing decomposability (Epilobium angustifolium and Calamagrostis epigeios). Additionally, we investigated the DOC transformation during soil passage in decomposition experiments and in the field for the sites SLB and SLS. For SLS, decomposition of Epilobium resulted in a cumulative CO₂ production of 14% of the added C within 128 days. Priming effects were negligible. CO₂ production for the experiments using Calamagrostis was less with 11% for SLB and 10% for SLS. Cumulative DOC production was markedly high in the Epilobium decomposition experiment, being 25 g m^–2, out of which 11 g m^–2 were Epilobium‐derived (2% of the added C). For the Calamagrostis experiments, cumulative productions of DOC and Calamagrostis‐derived DOC (0.1% of the added C for SLS and SLB) were much less. During the soil passage, much of the DOC was removed by sorption or decomposition processes. Field studies at SLS and SLB using ¹³C natural abundance showed that ¹³C distribution of soil organic matter increased with depth, probably mainly due to a discrimination of C isotopes by decomposing microorganisms. DOC, however, showed a depletion of ¹³C from –28γ PDB to –29γ (SLB at 40 cm) or –28 to –30γ (SLS at 20 cm) with depth, owing to preferential decomposition of ¹³C‐enriched substances or preferential adsorption. This study indicates that DOC production is strongly affected by litter composition and that significant changes in DOC composition may occur during its passage through a soil depth of 40 cm.     

Chemische Gewässerverunreinigung und Wassernutzung

Pollution by chemicals of natural water resources frequently impairs production of drinking water. Enrichment by refractory dissolved organic compounds is the main reason as can be easily observed in the river Rhine. Characterization of pollution is possible by analysis of individual compounds and by the ratios of parameters such as DOC, COD and UV-extinction. Experience shows that future water pollution control technology has to include physical-chemical processes for the elimination of refractory substances.      

Organic Matter Diagenesis in Acidic Mine Lakes

The significance of organic matter origin for carbon oxidation via sulfate and iron reduction in the sediments of three acid mine lakes is analyzed. Carbon reactivity was estimated by fitting first‐order expressions to measured rates. Carbon oxidation rates via sulfate and ferric iron reduction ranged from 3.4 to 4.7 mmol m^–2 d^–1 and resembled those reported for freshwater lakes. The estimated reaction constants increased from about 10^–3 a^–1 at the interface to the former mine grounds to 0.05 to 0.2 a^–1 at the current sediment‐water interface. Aquatic organic matter accounted for an estimated 45...75% of total carbon oxidation rates while it amounted only to about 5...14% of the total organic matter that had been deposited. The results of this study suggest that in highly acidic mine lakes the reactivity of the deposited organic matter can rapidly increase after flooding, enhancing carbon oxidation and internal neutralization rates in the sediments.     

Environmental effect of produced water from North Sea oil operations

Produced water from North Sea oil reservoirs contains substantial amounts (about 1g I⁻¹) of non-hydrocarbon organic matter, largely as salts of acetic, propionic and butyric acids, as well as some 20–40 mg I⁻¹ of dissolved hydrocarbons such as benzene, toluene and xylene. The non-hydrocarbon components originate in water in the oil-bearing formation. All of the organic matter can be accounted for, within analytical accuracy. The water also contains some 20–30 mg I⁻¹ of ammoniacal nitrogen and a number of inorganic components.At peak water production from production installations in the North Sea some 1−2 × 10⁵ tonnes yr⁻¹ of organic acids will be discharged in the U.K. sector of the North Sea.The ready biodegradability of the organic constituents and the low toxicity of produced water have been confirmed by direct measurement; acute toxicity is unlikely at dilutions of greater than 100 fold.Dispersion has been modelled and tested in the laboratory indicating some 1000 fold dilution within less than 50 m of the discharge.The laboratory studies are supported by field observations. Any direct deleterious effects are limited to the immediate vicinity of the discharge (within a few tens of metres).     

Use of a single-bowl continuous-flow centrifuge for dewatering suspended sediments: Effect on sediment physical and chemical characteristics

The use of a single-bowl continuous-flow centrifuge (CFC, Sharples-Pennwalt Model AS-12) for dewatering suspended sediment from large volumes of river water is evaluated. Sediment-recovery efficiency of 86-91 per cent is comparable to that of other types of CFC units. The recovery efficiency is limited by the particle-size distribution of the feed water and by the limiting particle diameter that is retained in the centrifuge bowl. The limiting particle diameter, using the parameters for this study (bowl radius = 10.5cm; bowl length = 71.1 cm; rotational velocity = 16000 r min^?1; flow rate = 2 L min^?1, and an assumed hydrated particle density = 1.7 gm cm^?3), is 370 nm. There seems to be no particle-size fractionation within the centrifuge bowl—the median particle size was the same at the top as at the bottom. Particle electrophoretic mobility plays some role in fractionation of particles within the centrifuge. The mobility ranged from ?1.19 to ?2.01 × 10^?8 m² V^?1 s^?1, which is typical of clays coated with organic matter, the charge of which is partially neutralized by divalent cations and iron. Contamination by trace metals and organics is minimized by coating all surfaces that come in contact with the sample with either FEP or PFA Teflon and using a removable FEP Teflon liner in the centrifuge bowl. Because of the physical and chemical factors affecting particle fractionation within the centrifuge, care must be exercised in interpreting the environmental consequences of particles collected by continuous-flow centrifugation.     

洪泽湖水沙变化趋势和冲淤时空分布及驱动因素

为了研究洪泽湖水沙特性、变化趋势与冲淤时空分布规律,运用累积距平法、Mann-Kendall趋势与突变检验以及R/S分析法等方法,分析了洪泽湖19502016年的水沙特征;采用地理信息技术,基于1992年和2016年实测地形,对湖区泥沙冲淤空间分布进行了定量计算与分析.结果表明,入湖径流量无明显增加或减少的趋势,输沙量和含沙量呈明显减小趋势,1990年以后含沙量基本稳定在0.2 kg/m^3以下;淮河干流(包括池河)入湖水量和沙量约占入湖总量的89.6%,三河闸出湖水沙占总出湖量的60%.淮干入湖口和溧河洼为主要淤积区域,淤积量分别为2300×10^4和1900×10^4 m^3,平均淤积厚度分别为0.35和0.25 m;其他区域自然冲淤基本平衡.上游水库和河道闸坝的拦沙作用、农业种植结构变化和水土保持、大规模人工采砂等是入湖沙量减少的主要影响因素;湖区水动力特性是泥沙自然淤积主导因素,而湖区库容变化的主因则是人工采砂、围湖造田和围网养殖,且人类活动的影响远大于自然冲淤.     

Solute transfer across the sediment surface of a eutrophic lake: I. Porewater profiles from dialysis samplers

Porewater profiles often are used to identify and quantify important biogeochemical processes occurring in lake sediments. In this study, multiple porewater profiles were obtained from two eutrophic Swiss lakes using porewater equilibrators (peepers) in order to examine spatial and seasonal trends in biogeochemical processes. Variability in profile shapes and concentrations was small on spatial scales of a few meters, but the uncertainty in calculated diffusive fluxes across the sediment surface was, on average, 35%. Focusing of Fe and Mn oxides toward the lake center resulted in systematic increases in porewater concentrations and diffusive fluxes of Fe²⁺ and Mn²⁺ with increasing water depth; these fluxes are postulated to be regulated by the pH-dependent dissolution of reduced-metal phases. Despite higher concentrations of inorganic carbon, NH ₄ ⁺ , Si and P in pelagic compared to littoral sites, diffusive fluxes of these substances across the sediment surface increased only slightly or not at all with increasing water depth. Porewater profiles did reveal temporal changes in Fe²⁺, Mn²⁺, Ca²⁺ and Mg²⁺ that were an indirect result of the large, seasonal changes in seston deposition, but no clear seasonal variations were found in diffusive fluxes of nutrients across the sediment surface. The intense mineralization occurring at the sediment surface was not reflected in the porewater profiles nor in the calculated diffusive fluxes. Calculated diffusive fluxes across the sediment surface resulted from decomposition occurring primarily in the top 5–7 cm of sediment. Diffusive fluxes from this subsurface mineralization were equal to the solute release from mineralization occurring at the sediment-water interface. Buried organic matter acts as a memory of previous lake conditons; it will require at least a decade before reductions in nutrient inputs to lakes fully reduce the diffusive fluxes into the lake from the buried reservoir of organic matter.     

Water Quality Assessment and Resource Potentials: the Case of Aba–Urban and its Environs,Niger Delta Basin

The quest for improved water supply to cater for the ever increasing population has given rise to the assessment of water quality and resource potentials in Aba-Urban and its environments. The area, which lies within the Niger Delta Basin is underlain by the Benin Formation that is highly aquiferous. Samples of sands and water were subjected to sedimentological and hydrochemical analysis, respectively. Result reveals that the aquifer is thick (over 100 m) and unconfined. The computed aquifer parameters indicate high yielding clean-sands with hydraulic conductivity values ranging from 1.13 × 10^–4 to 5.70 × 10^–3 m/s. The specific discharge is about 14.2 m/year while the average linear groundwater velocity is calculated to be 53.46 m/year. Hydrochemical investigations carried out on water samples from Aba River and the groundwater system revealed low dissolved geochemical constituents. Although, there is a slight increase from the north to the southern part along the flow path. In general, the groundwater is relatively enriched in Ca, Mg?HCO^-₃ions and is predominantly of bicarbonate constituents. However, in some places Cl^? ions dominate over HCO^-₃ions. This is common where the water has come in contact with domestic sewage. This kind of contamination is also accompanied by elevated concentration of NO^-₃ions. Generally, the groundwater in most cases meets the standard for human consumption and is a better alternative to surface water. Consequently an increase exploitation of the prolific Benin aquifer through more hygienic and safe methods will surely be the best way of improving the domestic water supply situation in Aba City.     

大渡河龚咀水库泥沙特性与淤积

龚咀水库库容3.1×10~8m~3,是大渡河上最大的水库,从1971年蓄水以来的15年间,淤积量达2.2096×10~8m~3,占库容的71.3％。淤积可分蓄水初期,三角洲发展和淤积接近平衡三个时期,其淤积率分别为83.5％,53％和2.9％。淤积物的平均粒径从1.82mm增加为3.38mm。卵砾推移质移动至坝前。淤积量变化过程即为输沙能力调整恢复过程。     

Cancer risk estimation from dietary arsenic,a new approach from longitudinal cohort study

Inorganic arsenic is a carcinogen and consumption in low dose may lead to cancer. We estimated the cancer risk of the participants from arsenic endemic regions of West Bengal, India. The probable cancer risk was estimated following the assessment of daily inorganic arsenic intake through drinking water and diets of 20 participants for three consecutive years who had been using low arsenic water in the Indian context (median arsenic concentration in the study Years-I, II and III were 22, 16, 13 µg/l respectively). Probable cancer risk of the population was 2.80 × 10^?4, 2.94 × 10^?4, 3.12 × 10^?4 in the three respective study years (Year-I, II and III); just higher than the US EPA risk level of concern. The arsenic species content of the paired raw, cooked rice and urine was estimated in the as is taken basis. The major diet component, rice contained 72–86% inorganic arsenic whereas urine contains 70% organic arsenic on an average. The cancer risk assessment has been proposed to be modified by inclusion of urine arsenic release, considering the fact of arsenic release through urine. The risk became 1.28 × 10^?5, 1.13 × 10^?5, 1.01 × 10^?5 in the study Year-I, II and III respectively, considering urinary arsenic release, attributed the consideration of urine arsenic release into probable cancer risk estimation.     

水位变化对干涸湖底沉积物有机碳矿化的影响

人为干扰和气候变化会改变湖泊水位状态,明确不同水位条件下湖泊沉积物有机碳矿化特征及其影响因素,对了解内陆水生态系统碳循环具有重要意义.为探究干旱区典型盐湖沉积物有机碳矿化速率对水位变化的响应,以巴里坤湖干涸湖底原状沉积物为研究对象,初步探究了0（T1）、-9（T2）、-23（T3）、-34（T4）和-45 cm（T5）水位处理对沉积物有机碳矿化速率的影响.结果表明,T1、T2和T3处理有机碳矿化速率在试验初期较高（0~10 d）,10 d后缓慢下降,T4和T5处理有机碳矿化速率呈先增加后降低趋势;T1（1.718 μmol/（m²·s））与T3（1.784 μmol/（m²·s））处理有机碳矿化速率不存在显著差异,T1处理有机碳矿化速率是T2、T4和T5处理的1.09、3.31和3.57倍,不同处理有机碳累积矿化量表现为T3 > T1 > T2 > T4 > T5.有机碳累积矿化量（C_t）占沉积物有机碳（C₀）的比例（C_t/C₀）介于0.012~0.044之间,沉积物有机碳潜在排放量（C_i）占C₀的比例（C_i/C₀）介于0.018~0.045之间;水位降低,沉积物有机碳矿化常数（k值）减小,T1处理k值最大（0.137 d）,T4处理最小（0.032 d）.线性方程C_r=0.008x+0.488能较好地模拟有机碳矿化速率（C_r）与水位（x）的关系;不同水位处理有机碳矿化速率与模拟柱中沉积物5 cm温度呈显著的指数函数关系,T4、T5处理有机碳矿化温度敏感系数（Q₁₀）显著高于T1、T2和T3处理,即水位降低增加了巴里坤湖干涸湖底沉积物Q₁₀.因此,就巴里坤湖干涸湖底沉积物而言,水位从0 cm降至-45 cm时有机碳矿化速率降低,Q₁₀增加;反之水位上升则会促进有机碳矿化分解,Q₁₀降低.水位持续下降抑制有机碳矿化可能是维持干旱区盐湖沉积物碳库稳定的机制之一.     

Cadmium,zinc, copper,and barium in foraminifera tests

The concentrations of cadmium, zinc, copper and barium have been determined on 2-mg samples of single-species foraminifera populations. Cleaning techniques were tested using North Atlantic core tops, and followed by a detailed downcore study for the last 30,000 years in South Atlantic core V22-174. Raw foram tests cleaned by crushing followed by ultrasonic removal of fine-grained material, and dissolved in a pH 5.5 acetate buffer, contain appreciable amounts of trace elements associated with ferromanganese and alumino-silicate contaminants. A reductive/complexing cleaning treatment reduces ferromanganese contamination by 1–2 orders of magnitude. Acetate buffers at pH 5.5 complex iron and raise the solubility of ferromanganese oxides; these buffers are unsuitable for separating carbonate lattice-bound trace elements from the fraction associated with ferromanganese phases. Improved mechanical and ultrasonic reductive cleaning combined with a mild dissolution in distilled water under 1 atm.P_CO2 reduces contaminant levels another order of magnitude. The Cd and Zn concentrations (order 10^?8 mole Cd/mole Ca and 10^?5 mole Zn/mole Ca) of species with low surface area show an increase with decreasing isotopic temperatures. This increase is consistent with the increasing concentrations of these metals from low values in surface waters to higher values at depth. The variance of Cd and Zn over the last 30,000 years in the central South Atlantic is consistent with the probable variability of the dissolved trace elements at the calcification levels of the species analyzed. Cu and Ba are irreproducible and probably sensitive to residual contaminant phases. The trace element content of the tests differs from levels observed in a recent coprecipitation study. Foraminifera may be a significant vector in zinc cycling in the ocean.     

Studies on the Pollution of the Kalinadi by Industrial Wastes Near Mansurpur Part 1: Hydrometric and Physico-Chemical Characteristics of the Wastes and River Water

Stream pollution by industrial wastes is posing a problem in Uttar Pradesh. In the present investigations an attempt has been made to study the ecological features of a section of the Kalinadi so as to find out the cumulative or detrimental effect of pollution on fish and fisheries by the effluent discharge of sugar factory and distillery wastes near Mansurpur (District Muzaffarnagar), U. P. This paper is part I of the project. The liquid wastes produced by the sugar factory vary from 66 × 10⁶ to 88 × 10⁶ litres/day excluding condenser water and contain variable quantities of cane fibres, cellulose, lime, waxes, fermented sugar juice, mollasses, and some quantities of sulphate, phosphate, and nitrogen, the oxygen being nil with high values of B. O. D. and C. O. D. The liquid waste from the distillery is called spent wash. The spent wash (62 × 10⁴ litres/day) is highly coloured and acidic (pH 4.3 … 2.9). The B. O. D. and C. O. D. values were very high in the order of 28,526 mg/1 … 45,146 mg/1 and 52,516 mg/1 to 66,862 mg/1. Thus total waste of about 17.3 × 10⁶ litres with no oxygen and high B. O. D. (9,600 mg/1 … 10,116 mg/1) is let off into the Kalinadi. Hydrometric observations on the Kalinadi show that the pollutional hazard is appreciable during the low flow period of the river. The wastes affect the river in a number of ways:

• - The deposition of cellulose fibres, organic and inorganic matter affects the substratum adversely. The blackish brown colour of the wastes affects the light penetration by limiting the growth of phytoplankton.
• - There appears to be no potential danger to the river from the electrolyte pollution as the specific conductivity lies below limiting values.
• - Changes in pH in river water due to the acidic nature of the wastes do not affect directly the fauna and flora, but the acidic condition becomes lethal in the presence of low oxygen and high temperature values.
• - The high load of organic matter present in the wastes draws heavily on the oxygen budget of the river and adversely changes the water and bottom quality of the river for a stretch of 10 km, which adversely affects the environmental condition of both fish and fish food.
• - The presence of sulphuric acid in distillery waste and hydrogen sulphide in river water is toxic to fish and fish food.
• - The decomposition of organic matter in an anaerobic condition and in another favourable environment, as with a low redox potential, the presence of sufficient organic matter and a constant supply of sulphur-reducing bacteria, produces more hydrogen sulphide which may be detrimental or sublethal in the presence of a low oxygen saturation and high temperature.
• - The oxygen level increases at each succeeding station through reaeration and dilution with the lowering of B. O. D. and C. O. D. The oxygen-sag curve is like a typical spoon with handle-shape.

     

Determination of Trace Levels of Nickel and Manganese in Soil,Vegetable, and Water

A simple and reliable method for rapid and selective extraction and determination of trace levels of Ni²⁺ and Mn²⁺ was developed by ionic liquid (IL) based dispersive liquid–liquid microextraction coupled to flame atomic absorption spectrometry (FAAS) detection. The proposed method was successfully applied to the preconcentration and determination of nickel and manganese in soil, vegetable, and water samples. After preconcentration, the settled IL‐phase was dissolved in 100 µL of ethanol and aspirated into the FAAS using a home‐made microsample introduction system. Injection of 50 µL of each analyte into an air–acetylene flame provided very sensitive spike‐like and reproducible signals. Effective parameters such as pH, amount of IL, volume of the disperser solvent, concentration of the chelating agent, and effect of salt concentration were inspected by a (2^5‐1) fractional factorial design to identify the most important parameters and their interactions. Under optimum conditions, preconcentration of 10 mL sample solution permitted the detection of 0.93 µg L^?1 Ni²⁺ and 0.52 µg L^?1 Mn²⁺ with enrichment factors 77.2 and 82.6 for Ni²⁺ and Mn²⁺, respectively. The accuracy of the procedure was evaluated by analysis of a certified reference material (CRM TMDW‐500, drinking water).     

Estimation of heat discharge rates using infrared measurements by a helicopter-borne thermocamera over the geothermal areas of Unzen volcano, Japan

Unzen volcano is situated on Shimabara Peninsula, western Kyushu, Japan. On the flank of the volcano, the Obama, Unzen and Shimabara hot springs are aligned in a direction from the southwest to the northeast across the peak. At Obama and Shimabara, heat is transferred mainly by water flow. But at Unzen heat is transferred by the discharge of natural steam and by conduction as well as water flow. In order to estimate the heat discharge by mechanisms other than water flow, infrared measurements by a helicopter-borne thermocamera were conducted over the Unzen hot spring area. The heat discharge was calculated from the thermal image by a method based on heat balance of the ground surface resulting in a value of 1.9 × 10⁶ cal/s (7.9 MW). The heat discharged by all mechanisms including that by water flow is estimated to be 5.0 × 10⁶ cal/s (21 MW). Similar preliminary estimates have been made for heat discharge at the Obama and Shimabara hot springs giving values of about 1.2 × 10⁷ cal/s (50 MW) and 1.0 × 10⁵ cal/s (0.4 MW), respectively. These values indicate that the heat discharge decreases with distance from the southwest to the northeast direction across the volcano. The total heat discharge from three hot spring areas on Unzen volcano is about 1.7 × 10⁷ cal/s (71 MW).The heat balance method appears useful for quantitative analysis of regional trends but its accuracy may not be always sufficient for detailed surveys. Several methods of determining heat flow, including the heat balance method, were compared at a test field in the Unzen hot spring area. The values obtained by the heat balance method coincide roughly with the other results but more detailed analysis is necessary to improve the accuracy of current methods of geothermal measurements.     

Surfactant Enhance DLLME/FO‐LADS: Assay of Malachite Green Level in Aquatic Environment of Trout Fish

Malachite green (MG), a traditional agent used in aquaculture although is not approved; its low cost and high efficacy make illicit use likely. We developed a small‐scale, simple, and sensitive dispersive liquid–liquid microextraction procedure for the assay of trace amounts of MG in aquatic environment of Trout fish. Fiber optic‐linear array detection spectrophotometry with charge‐coupled device detector benefiting from a microcell was used for this purpose. The method is based on enhancement effect of an anionic surfactant on the extraction of MG in to very fine multidroplets of microextraction solvent which made assisted by disperser solvent. Under the optimum conditions, the enrichment factor 77.5 was obtained from a 5‐mL water sample. The calibration graph was linear up to 5 × 10^?7 mol L^?1 with detection limit of 1 × 10^?8 mol L^?1. The relative standard deviation for seven replicate measurements of 4 × 10^?7 and 5 × 10^?8 mol L^?1 of MG were 3.3 and 4.5%, respectively.