Simulation von Variablen der Fließgewässerqualität mittels Mehrfachregressionen

There are investigated the variables O₂, BOD₅, seston, NO₃-N, NH₄-N and o-PO₄ from at least five-year series of five stations along a river section of 50 km. After exclusion of a linear trend and substraction of the individual monthly mean values from the monthly mean of many years in order to eliminate the effect of the annual variation as well as testing for normal distribution, first the correlation coefficients of the variables to the flow rate Q and the temperatures of air and water are determined, which show directional changes just in the longitudinal profile of the river. The same holds for the correlation of the variables between the measuring points. From this the model structure is derived, according to which the concentration at one measuring station can be simulated by multiple regression to Q and T at the same level as well as the concentration at the upper level. The results are discussed in detail and evaluated with respect to their inclusion in longterm management models of water quantity management.     

Polarographische Bestimmung von Schwermetallen im Klärschlamm

The differential-pulse polarography (DPP) and the stripping voltametry (SV) are investigated in detail with respect to their suitability for the quantitative detection of individual traces of heavy metals in sewage sludge. The results are checked on the basis of AAS analyses and by the standard-addition method. From the hydrochloric-acid extracts of fused sludge samples down to 1 μg/l can be detected by the SV, whereas the DPP reaches a sensitivity of 100 μg/l. The following basic electrolytes are used: Zn: 2 … 3 mol/l H₃PO₄; Cu: 0.4 mol/l K₂CO₃, 0.2 mol/l Na-K-tartrate, 0.1 mol/l HCl; Ni: 1 mol/l NH₄OH, 1 mol/l NH₄Cl, 25 ml/l triethylamine; Pb and Cd: 0.1 … 0.2 mol/l HCl.     

Enhancement of Carbon Dioxide Capture by Amine‐Functionalized Multi‐Walled Carbon Nanotube

In this study, crude multi‐walled carbon nanotubes (MWCNT) was functionalized by a two‐step process; first using strong mixed acids (H₂SO₄/HNO₃) and then treatment with 1,3‐phenylenediamine (mPDA). The equilibrium adsorption of CO₂ on pristine MWCNT and amine functionalized MWCNT (MWCNT‐NH₂) were investigated. Experiments were preformed via application of volumetric method in a dual sorption vessel at temperature range of 298–318 K and pressures up to 40 bars. The results obtained indicated that the equilibrium uptake of CO₂ increased after functionalizing of MWCNT. The increase in CO₂ capture by MWCNT‐NH₂ was attributed to the existence of great affinity between CO₂ molecules and amine sites on this adsorbent at low pressures. The experimental data were analyzed by means of Freundlich and Langmuir adsorption isotherm models. The data obtained revealed a fast kinetics for the adsorption of CO₂ in which most of adsorption occurred at initial period of adsorption experiments. This renders MWCNT as a suitable adsorbent for practical applications. Values of isosteric heat of adsorption were evaluated based on Clausius–Clapeyron equation. The results demonstrated that both chemisorption and physisorption played important role in CO₂ adsorption on MWCNT‐NH₂, whereas the physisorption process was dominant for CO₂ adsorption on MWCNT.     

太湖霍甫水丝蚓(Limnodrilus hoffmeisteri) NH4+-N和PO43--P的潜在释放量

为了研究太湖底栖动物优势种类——霍甫水丝蚓(Limnodrilus hoffmeisteri)对于湖泊富营养化的影响,以温度和密度为模拟控制条件,对太湖霍甫水丝蚓进行营养盐释放的室内控制实验,研究温度和密度的变化对霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P释放率的影响,根据霍甫水丝蚓铵态氮(NH_4~+-N)和磷酸盐(PO_4~(3-)-P)释放率与温度的关系方程,结合太湖霍甫水丝蚓2007-2010年的生物量估算其对太湖水体氮磷的潜在贡献.结果表明,随温度升高太湖霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P的释放率均呈现逐渐升高的趋势,而密度变化对霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P释放率的影响均不显著,太湖霍甫水丝蚓NH_4~+-N和PO_4~(3-)-P年平均释放量分别为1925.5和210.0 t,分别可达到全太湖沉积物-水界面NH_4~+-N和PO_4~(3-)-P的年净通量的19.3%和23.3%,表明霍甫水丝蚓的营养盐释放对于湖泊生物地化循环和湖泊富营养化具有显著的影响.     

Nested‐Scale Nutrient Flux in a Mixed‐Land‐Use Urbanizing Watershed

To improve quantitative understanding of mixed‐land‐use impacts on nutrient yields, a nested‐scale experimental watershed study design (n = 5) was applied in a 303(d), clean water act impaired urbanizing watershed of the lower Missouri River Basin, USA. From 2010 to 2013, water samples (n = 858 sample days per site) were analysed for total inorganic nitrogen (TIN‐N), nitrite (NO₂–N) nitrate (NO₃–N), ammonia (NH₃–N), and total phosphorus (TP‐P). Annual, seasonal, and monthly flow‐weighted concentrations (FWCs) and nutrient yields were estimated. Mean nutrient concentrations were highest where agricultural land use comprised 58% of the drainage area (NH₃ = 0.111 mg/l; NO₂ = 0.045 mg/l; NO₃ = 0.684 mg/l, TIN = 0.840 mg/l; TP = 0.127 mg/l). Average TP‐P increased by 15% with 20% increased urban land use area. Highly variable annual precipitation was observed during the study with highest nutrient yields during 2010 (record setting wet year) and lowest nutrient yields during 2012 (extreme drought year). Annual TIN‐N and TP‐P yields exceeded 10.3 and 2.04 kg ha^?1 yr^?1 from the agricultural dominated headwaters. Mean annual NH₃–N, NO₂–N, NO₃–N, TIN‐N, and TP‐P yields were 0.742, 0.400, 4.24, 5.38, and 0.979 kg ha^?1 yr^?1, respectively near the watershed outlet. Precipitation accounted for the majority of the explained variance in nutrient yields (R² values from 0.68 to 0.85). Nutrient yields were also dependent on annual precipitation of the preceding year (R² values from 0.87 to 0.91) thus enforcing the great complexity of variable mixed‐land‐use mediated source‐sink nutrient yield relationships. Study results better inform land managers and best management practices designed to mitigate nutrient pollution issues in mixed‐land‐use freshwater ecosystems. Copyright © 2015 John Wiley & Sons, Ltd.     

Aqueous volatiles in hydrothermal fluids from the Main Endeavour Field, northern Juan de Fuca Ridge: temporal variability following earthquake activity

The Main Endeavour Field, northern Juan de Fuca Ridge, experienced intense seismic activity in June 1999. Hydrothermal vent fluids were collected from sulfide structures in September 1999 and July 2000 and analyzed for the abundance of H₂, H₂S, CH₄, CO₂, NH₃, Mg and Cl to document temporal and spatial changes following the earthquakes. Dissolved concentrations of CO₂, H₂, and H₂S increased dramatically in the September 1999 samples relative to pre-earthquake abundances, and subsequently decreased during the following year. In contrast, dissolved NH₃ and CH₄ concentrations in 1999 and 2000 were similar to or less than pre-earthquake values. Aqueous Cl abundances showed large decreases immediately following the earthquakes followed by increases to near pre-earthquake values. The abundances of volatile species at the Main Endeavour Field were characterized by strong inverse correlations with chlorinity. Phase separation can account for 20-50% enrichments of CO₂, CH₄, and NH₃ in low-chlorinity fluids, while temperature- and pressure-dependent fluid-mineral equilibria at near-critical conditions are responsible for order of magnitude greater enrichments in dissolved H₂S and H₂. The systematic variation of dissolved gas concentrations with chlorinity likely reflects mixing of a low-chlorinity volatile-enriched vapor generated by supercritical phase separation with a cooler gas-poor hydrothermal fluid of seawater chlorinity. Decreased abundances of sediment-derived NH₃ and CH₄ in 1999 indicate an earthquake-induced change in subsurface hydrology. Elevated CO₂ abundances in vent fluids collected in September 1999 provide evidence that supports a magmatic origin for the earthquakes. Temperature-salinity relationships are consistent with intrusion of a shallow dike and suggest that the earthquakes were associated with movement of magma beneath the ridge crest. These data demonstrate the large and rapid response of chemical fluxes at mid-ocean ridges to magmatic activity and associated changes in subsurface temperature and pressure.     

Variations in trace gas concentrations in different environments in India

Observations of trace gases (SO₂, NH₃, NO₂ and O₃) were made during the period 1981 to 1984 at 6 different locations representative of urban industrial, urban, nonurban, thermal power plant and marine environment. Diurnal variations of the trace gases were studied in an urban environment. Except in the urban industrial environment, the concentration of NH₃ was found in the range of background values. Also, the average concentrations of NO₂ and O₃ at the different environments were in the order of background values. However, the concentrations of SO₂ were substantially higher by about 7 times, in urban industrial and thermal power plant environments. The diurnal variations of SO₂, NH₃ and NO₂ showed anitphase relationship with surface temperature at the urban environment station which is relatively free of industrial pollution. Discussion is centred on trace gas variations in different environments in India together with the values reported for various countries in the world.     

Änderungen der chemischen Eigenschaften des Klärschlammes bei der Methanfermentation

Zusammenfassung Im Verlauf der anaeroben Fermentation des Kl?rschlammes kommt es zu ?nderungen der chemischen Eigenschaften. Die organischen Stoffe werden in wasserl?sliche Verbindungen mit niedrigerem Molekülgewicht, diese dann weiter in Mineralkomponenten CH₄, CO₂, NH₃ und H₂S zersetzt. In der vorliegenden Arbeit sind diese ?nderungen quantitativ ausgewertet, und die Kinetik ihres Verlaufes wurde verfolgt. Die erzielten Ergebnisse sind in Tabellen und Abbildungen zusammengefasst.

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Summary The anaerobic methane fermentation of sewage sludge caused changes of its chemical properties. Organic matter is decomposed into water soluble compounds of minor molecular weight, and subjected to further decomposition into mineral components CH₄, CO₂, NH₃ and H₂S. This paper deals with these changes in a quantitative evaluation, the kinetics of their course being followed as well. The attained results are summarized into tables and graphs.

     

Full‐scale Applications of Membrane Filtration in Municipal Wastewater Treatment Plants

The performance of one pilot‐scale and two full‐scale membrane bioreactors (MBR) were evaluated based on the control of main operational parameters, composition of microbial community and pathogens concentration in the treated outlet. Plants were designed for 0.75 m³/day (A), 60 m³/day (B) and 30 m³/day (C). Inlet and outlet samples were monitored for chemical oxygen demand (COD), biological oxygen demand, total suspended solids, ammonia nitrogen concentration (NH₄–N), nitrate nitrogen concentration, total Kjeldahl nitrogen, total phosphorus and phosphate phosphorus concentration concentrations. Plants showed good COD removal: 91.9% for Plant A, 97.8% for Plant B and 94.2% for Plant C. The targeted nitrogenous ion was NH₄–N due to the requirements for outlet limits. NH₄–N removal was moderate for Plant A (73.3%) and Plant B (86.1%) and excellent for Plant C (>99%). Excellent phosphorus removal was achieved by Plant A (average outlet concentration was 0.7 mg/L, efficiency 84.7%). Unsatisfactory results for phosphorus removal were achieved at the full‐scale plants due to operational problems. The dependency between the extracellular polymeric substances increase and decreasing mixed liquor volatile suspended solids for both lab and full‐scale plants was confirmed. Soluble microbial product concentrations were reduced by 65–68% after coagulant dosage for Plant A. Outlets from the MBR plants were monitored for the presence of pathogens (thermotolerant coliforms, Escherichia coli, intestinal Enterococci and culturable microorganisms at 22 and 37°C). The treated effluent from Plant A, B and C met Czech national legislation regarding reuse criteria (standards) for environment, irrigation and swimming purposes. Plants B and C were not able to achieve requirements for potable water and personal hygiene quality standards.     

Catalytic Reduction of Hexaminecobalt(III) by Pitch‐based Spherical Activated Carbon (PBSAC)

The wet ammonia (NH₃) desulfurization process can be retrofitted to remove nitric oxide (NO) and sulfur dioxide (SO₂) simultaneously by adding soluble cobalt(II) salt into the aqueous ammonia solution. Activated carbon is used as a catalyst to regenerate hexaminecobalt(II), Co(NH₃), so that NO removal efficiency can be maintained at a high level for a long time. In this study, the catalytic performance of pitch‐based spherical activated carbon (PBSAC) in the simultaneous removal of NO and SO₂ with this wet ammonia scrubbing process has been studied systematically. Experiments have been performed in a batch stirred cell to test the catalytic characteristics of PBSAC in the catalytic reduction of hexaminecobalt(III), Co(NH₃). The experimental results show that PBSAC is a much better catalyst in the catalytic reduction of Co(NH₃) than palm shell activated carbon (PSAC). The Co(NH₃) reduction reaction rate increases with PBSAC when the PBSAC dose is below 7.5 g/L. The Co(NH₃) reduction rate increases with its initial concentration. Best Co(NH₃) conversion is gained at a pH range of 2.0–6.0. A high temperature is favorable to such reaction. The intrinsic activation energy of 51.00 kJ/mol for the Co(NH₃) reduction catalyzed by PBSAC has been obtained. The experiments manifest that the simultaneous elimination of NO and SO₂ by the hexaminecobalt solution coupled with catalytic regeneration of hexaminecobalt(II) can maintain a NO removal efficiency of 90% for a long time.     

Net, actual, and potential sediment-water interface NH4 fluxes in the northern Gulf of Mexico (NGOMEX): Evidence for NH4 limitation of microbial dynamics

A new approach, combining ¹⁵NH₄⁺ isotope dilution and continuous-flow techniques, provided estimates of “actual” and “net” NH₄⁺ flux and sediment NH₄⁺ demand (SAD) at the sediment-water interface (SWI) of sites in the northern Gulf of Mexico (NGOMEX). The sites included a hypoxic site (C6), two sites with intermediate oxygen levels (B7 and F5), and a normoxic site (CT). Control cores without isotope addition and other cores from the same site treated with ¹⁵NH₄⁺ labeled overflowing water differentiated between net and actual regeneration flux and actual vs. potential uptake flux of NH₄⁺. Experiments were conducted in 2008 before (July) and after (September) two successive hurricanes (Gustav and Ike) and in January and August, 2009. Actual regeneration was significantly higher than net flux at most sites. Net flux did not differ significantly in most sites/dates, but the actual regeneration, and the actual and potential uptake, showed temporal and spatial variation; the flux at the hypoxic site was more active than non-hypoxic sites. SAD, the difference between potential and actual NH₄⁺ uptake flux, was higher at the hypoxic site than at non-hypoxic sites before and after the hurricanes in 2008 and during the hypoxia season in 2009. SAD related negatively to bottom water DO values. Conclusions: (1) net flux often underestimated actual regeneration, (2) hurricane activity decreased N dynamics, and (3) microbial N limitation status at the hypoxic site related to NH₄⁺ removal processes that were independent of oxygen (e.g., anaerobic heterotrophic uptake or anammox). These results indicate a rather consistent NH₄⁺ demand at the SWI during the hypoxic season and suggest that reduced nitrogen may limit microbial dynamics in the region.     

Influences of watershed landscape composition and configuration on lake‐water quality in the Yangtze River basin of China

Lake‐water quality is highly dependent on the landscape characteristics in its respective watershed. In this study, we investigated the relationships between lake‐water quality and landscape composition and configuration within the watershed in the Yangtze River basin of China. Water quality variables, including pH, electrical conductivity (EC), dissolved oxygen (DO), Secchi depth (SD), NO₂^?, NO₃^?, NH₄⁺, TN, TP, chemical oxygen demand (COD_Mn), chlorophyll‐a (Chl‐a), and trophic state index (TSI), were collected from 16 lakes during the period of 2001–2003. Landscape composition (i.e. the percentage of vegetation, agriculture, water, urban, and bare land) and landscape configuration metrics, including number of patches (NP), patch density (PD), largest patch index (LPI), edge density (ED), mean patch area (MPA), mean shape index (MSI), contagion (CONTAG), patch cohesion index (COHESION), Shannon's diversity index (SHDI), and aggregation index (AI), were calculated for each lake's watershed. Results revealed that the percentage of agriculture was negatively related to NO₂^?, TN, TP, Chl‐a concentrations, and TSI, while the percentage of urban was significantly correlated with EC, NH₄⁺, and COD_Mn concentrations. Among landscape‐level configuration metrics, only ED showed significant relationships with TN, TP concentrations, and TSI. However, at the class level, the PD, LPI, ED, and AI of agriculture and urban land uses were significantly correlated with two or more water quality variables. This study suggests that, for a given total area, large and clustered agricultural or urban patches in the watershed may have a greater impact on lake‐water quality than small and scattered ones. Copyright © 2011 John Wiley & Sons, Ltd.     

Dynamische Modellierung des pH-Einflusses bei der Nitrifikation hochbelasteter Abwässer Dynamic Modelling of the pH Influence in Nitrification of Highly Concentrated Wastewater

Wastewater with high ammonia concentrations is produced by many industries, e.g. in the production of fertilizer and explosives and in the agricultural and food industry. A direct discharge into rivers and lakes has to be avoided: Oxidation of ammonia requires 4.56 g DO/g NH⁺₄-N and results in a decrease of dissolved oxygen concentration. Moreover, nitrate stimulates the proliferation of algae, with regard to the eutrophication of natural waters. For municipal wastewater with an ammonia concentration less than 50 mg/L NH⁺₄-N nitrification is a standard process. However, the removal of higher loaded industrial effluents still poses many questions. Recently, lab-scale and pilot-scale investigations show remarkable advances in the increase in nitrification efficiency and in the stabilization of the process. But because of changing flowrates and concentrations, the aid of advanced control algorithms is necessary. Some of the most important variables of biochemical reactors can be determined only with difficulty, at times only with off-line measurements. Model-aided measurement approaches try to determine these variables indirectly from easily measured variables. An experimentally-proved reactor model is required. Therefore, a dynamic model of nitrification in ideally mixed reactors is proposed based on mass balances for the components ammonia. nitrite, nitrate. dissolved oxygen DO, carbon dioxide, pH. nitrosomonas and nitrobacter. The biological reaction rates consider oxygen limitation and substrate inhibition. The process model presented is tested by lab scale experiments using an aerated stirred tank reactor and a fluidized bed reactor. Conformity between the predictions of the model and the observed data was positive. It has been shown that the nitrite oxidation by nitrobacter is the most sensible step in nitrification.     

气象条件对淀山湖水质的影响

根据2007-2014年淀山湖湖体每月高锰酸盐指数(CODMn)、氨氮(NH3-N)、总氮(TN)和总磷(TP)等水质资料和青浦区气象局月平均气温、降水量和日照时数等气象资料,运用数理统计方法和特征值比较法分析淀山湖湖体CODMn、NH3-N、TN和TP等水质资料变化规律及温度、降水和日照时数等对水质的影响.结果表明:(1)气象条件影响淀山湖湖体水质.平均气温、日照时数影响NH3-N、TN和TP浓度,表现在平均气温高、日照时数多,NH3-N、TN浓度降低,相反平均气温低、日照时数少,NH3-N、TN浓度升高;平均气温高,也会使TP浓度上升,平均气温低,TP浓度降低.降水对水体中CODMn、NH3-N和TN等浓度有稀释作用,降水量多的月份其浓度偏低,相反降水量少的月份其浓度偏高.(2)受气象条件影响,CODMn、NH3-N、TN和TP有季节变化.CODMn浓度4-9月较高,10月翌年3月较低;NH3-N、TN浓度最高值出现在2-4月前后,最低值出现在7-10月;TP浓度最高值出现在7-8月,最低值出现在10月翌年5月.(3)淀山湖CODMn、NH3-N、TN和TP浓度呈下降趋势.     

曝气充氧对城市污染河道内源铵态氮释放的控制

以城市污染河道沉积物和上覆水为研究对象,利用模拟实验方法,探讨不同曝气充氧方式(水曝气EW、底泥曝气ES)对污染河道內源铵态氮(NH4+-N)释放的影响.研究结果发现:从间隙水和沉积物中NH4+-N的削减效果来看,底泥曝气均要优于水曝气;实验结束后,底泥曝气组沉积物与间隙水中NH4+-N含量分别减少63.39%和43.33%,水曝气组分别减少了7.54%和13.98%;从沉积物-水界面NH4+-N的扩散通量变化来看,水曝气组界面通量高于对照组,其变化规律与对照组相似;底泥曝气组沉积物-水界面NH4+-N扩散通量变化过程完全不同于其它两组,在整个试验周期内(除第5 d以外),底泥曝气组的通量低于水曝气组,在第15 d最低,为13.73 mg/(m2.d),仅为水曝气组和对照组的14.68%和19.93%,表明底泥曝气组沉积物NH4+-N的释放潜力低于水曝气组沉积物.     

Changes in the patterns of inorganic nitrogen and TN/TP ratio and the associated mechanism of biological regulation in the shallow lakes of the middle and lower reaches of the Yangtze River

The changes of NH₃-N, NO₃-N, NO₂-N and TN/TP were studied during growth and non-growth season in 33 subtropical shallow lakes in the middle and lower reaches of the Yangtze River. There were significant positive correlations among all nutrient concentrations, and the correlations were better in growth season than in non-growth season. When TP>0.1 mgL^?1, NH₃-N increased sharply in non-growth season with increasing TP, and NO₃-N increased in growth season but decreased in non-growth season with TP. These might be attributed to lower dissolved oxygen and low temperature in non-growth season of the hypereutrophic lakes, since nitrification is more sensitive to dissolved oxygen and temperature than antinitrification. When 0.1 mgL^?1>TP>0.035 mgL^?1, TN and all kinds of inorganic nitrogen were lower in growth season than in non-growth season, and phytoplankton might be the vital regulating factor. When TP<0.035 mgL^?1, inorganic nitrogen concentrations were relatively low and NH₃-N, NO₂-N had significant correlations with phytoplankton, indicating that NH₃-N and NO₂-N might be limiting factors to phytoplankton. In addition, TN/TP went down with decline in TP concentration, and TN and inorganic nitrogen concentrations were obviously lower in growth season than in non-growth season, suggesting that decreasing nitrogen (especially NH₃-N and NO₃-N) was an important reason for the decreasing TN/TP in growth season. The ranges of TN/TP were closely related to trophic level in both growth and non-growth seasons, and it is apparent that in the eutrophic and hypertrophic state the TN/TP ratio was obviously lower in growth season than in non-growth season. The changes of the TN/TP ratio were closely correlated with trophic levels, and both declines of TN in the water column and TP release from the sediment were important factors for the decline of the TN/TP ratio in growth season.     

Geochemische und 13C/12C-isotopenchemische Untersuchung zur Herkunft der Kohlensäure in mineralhaltigen Wässern Nordhessens (Deutschland)

Geochemical and ¹³C/¹²C-isotopical Investigation of Mineral Waters in Northern Hessia (Germany) and the Origin of their CO₂ Content The dissolved carbonate originates from three sources: 1. biogenetic soil-CO₂, 2. volcanic CO₂ related to the evaporites of the Zechstein formation, and 3. carbonate derived from the dissolution of limestones and dolomites. Miocenic basaltic melts penetrated the evaporites of the Zechstein, and the related CO₂ was trapped in the intra- and intergranulars of the salt minerals. Circulating meteoric waters dissolve the salt minerals releasing CO₂ gas. Thus, the occurrence of basalt is related to the CO₂ contents of the evaporites, and the dissolution of only small amounts of salts rich in CO₂ may result in a high concentration of carbonic acid. In waters rich in carbonate, where volcanic CO₂ dominates over the other two sources of carbon, a δ¹³C-value of “salt-CO₂” of about –1‰ (PDB) is obtained. Water with less dissolved carbonate species have smaller quantities of salt-CO₂ down to about 20%.     

Chemical Composition of Dew Resulting from Radiative Cooling at a Semi-arid Site in Agra, India

Dew samples were collected between October 2007 and February 2008 from a suburban site in Agra. pH, conductivity, major inorganic ions (F^?, Cl^?, NO ₃ ^? , SO ₄ ^2? , Na⁺, K⁺, Ca²⁺, Mg²⁺, and NH ₄ ⁺ ), and some trace metals (Cr, Sn, Zn, Pb, Cd, Ni, Mn, Fe, Si, Al, V, and Cu) were determined to study the chemistry of dew water. The mean pH was 7.3, and the samples exhibited high ionic concentrations. Dew chemistry suggested both natural and anthropogenic influences, with acidity being neutralized by atmospheric ammonia and soil constituents. Ion deposition flux varied from 0.25 to 3.0?neq?m^?2?s^?1, with maximum values for Ca²⁺ followed by NH ₄ ⁺ , Mg²⁺, SO ₄ ^2? , Cl^?, NO ₃ ^? , Na⁺, K⁺, and F^?. Concentrations of trace metals varied from 0.13 to 48?μg?l^?1 with maximum concentrations of Si and minimum concentration of Cd. Correlation analysis suggested their contributions from both crustal and anthropogenic sources.     

影响浙江西苕溪底栖动物分布的关键环境变量指示种的筛选

利用2003年西苕溪TM数据和DEM模型计算了55个样点上游3种空间尺度下(亚流域、河岸带和局部)的土地利用类型,通过冗余分析筛选出能够在显著水平上最大程度解释西苕溪流域底栖动物分布的最小变量组合——氨氮、荫蔽度、电导率、亚流域农田百分比以及栖境复杂度.方差分解结果表明氨氮是研究区域影响底栖动物分布的最重要环境变量,亚流域尺度农田百分比也是一个重要影响变量.在50%-100%适合度范围内最终筛选得到短脉纹石蛾Cheumato-psyche sp.1和Cheumatopsyche sp.2作为关键环境变量指示种.在一定范围内短脉纹石蛾的数量随着水体氨氮浓度和亚流域尺度农田百分比的上升而增加.短脉纹石蛾分布广泛、采集容易、具备一定的耐污能力和主动漂流能力、幼虫个体较大且在水中的生活史较长以及具有一定的生态可塑性等优点决定了短脉纹石蛾可以作为西苕溪流域的受干扰水体氨氮和亚流域尺度农田百分比的指示种.     

Der Einfluß von Erdölkohlenwasserstoffen auf die Primärproduktion des Donauplanktons

Danube river water samples were saturated with mineral oil, and then the primary production (gross) was determined by means of the light-dark bottle method (oxygen) in situ at depths of 0.1… 1.5 m in comparison with untreated samples. Samples were exposed for half a solar day alternately during the first and second half-days. Investigations carried out between March and October for periods of 14 days showed a mean production of 2.56 g · m^?2d^?1 O₂, which was reduced by 36% due to 12.6 mg/l hydrocarbons. Production decreases with the water depth from 6.2 to 0.9 mg · l^?1d^?1 0₂, whereas the inhibition by hydrocarbons increases from 31 to 41%.