EFFECTS OF PLACER GOLD MINING ON PRIMARY PRODUCTION IN SUBARCTIC STREAMS OF ALASKA1

ABSTRACT: Turbidity, total residues, settleable solids, vertical light extinction, and primary production were measured in mined and unmined streams located in the interior highlands of Alaska. Undisturbed streams had low turbidities (< 1 NTU), total residue concentrations averaging 120 mg 1^?1, and undetectable settleable solids. During active mining, turbidity, total residues, and settleable solids levels in a moderately mined stream averaged 170 NTU, 201 mg 1^?1, and < 0.1 ml 1^?1, respectively. In a heavily mined stream, turbidity and total residues were two orders of magnitude higher than in unmined streams and settleable solids nearly always exceeded 0.2 ml 1^?1. Vertical extinction coefficients and turbidity were positively correlated. In undisturbed streams gross primary productivity (g-O₂m^?2d^?1) ranged from 0.20 shortly after spring breakup to a maximum of 1.20 in early fall. Productivity in the moderately mined stream was reduced by 50 percent while photosynthetic efficiency doubled. Primary production was undetectable in a heavily mined stream. Maximum standing crops of periphyton measured as chlorophyll a occurred in fall in an undisturbed stream after 13 weeks of exposure and ranged from 4.5 to 11.8 mg-chl a m^?2. The highest chlorophyll a densities recorded in the moderately mined stream was 3.8 mg m^?2, and no chlorophyl a was detected in the heavily mined stream.     

Sensitivity of the zebrafish (Danio rerio) early life stage test for compounds with different modes of action

The sensitivity of the early life stage (ELS) toxicity test for two compounds with different modes of action was determined, and related to other toxicity tests with the same compounds. The zebrafish. Danio rerio, was used as a test organism, and the two model compounds were 1,2,3-trichlorobenzene (123TCB), a non-polar narcotic, and parathion, an acetylcholinesterase (AChE) inhibitor. Hatching and survival after 28 days were significantly reduced in the highest 123TCB treatment (263 microg/l), but not in any of the parathion treatments. Growth of the larvae was negatively affected at parathion concentrations above 20 microg/l, while AChE was only significantly inhibited at the highest concentration, 93 microg/l. No effects on growth were found in the 123TCB treatments. In comparison with acute and chronic studies with both compounds, the ELS test turned out to be less sensitive than chronic studies and more sensitive than acute studies. The difference in sensitivity between the tests systems seems however, to depend on the mode of action of the compound.     

Bioaccumulation of selected organochlorines in bats and tits: Influence of chemistry and biology

We analyzed six organochlorine compounds (HCB, lindane, p,p’-DDE, PCB # 138, #153, and # 180) from populations of the European great tit (Parus major) and from five species of bats (Pipistrellus pipistrellus, Nyctalus noctula, Plecotus auritus, Plecotus austriacus, Myotis myotis). A weak positive correlation between K_ow (n-octanol /water partition coefficient) and bioaccumulation (measured as residue values) was found within each species. However, the ratio of the concentrations in bats compared to titmice increased significantly with increasing K_ow. We argue that this is explained by the intensive juvenile feeding through long-term lactation and thus by the more intensive transfer of strongly lipophilic xenobiotics from mother to juvenile in mammals compared to birds. Further, there were clear variations between bat species with ranges of up to 11 times the lowest value for a single compound. These differences are related to different feeding habits of the adults and to different species-specific life history traits, such as age at maturity and number of offspring.     

AOX Formation and Elimination in the Oxidative Treatment of Synthetic Wastewaters in a UV-Free Surface Reactor (6 pp)

Intention, Goal, Scope, Background The effect of chloride concentration and pH on the UV oxidation systems was examined. Phenol and methanol were used as organic substances. The treatment of these chemicals by UV oxidation using a newly developed lab scale pretest UV-Free Surface Reactor (UV-FSR) with and without Cl– addition at different pH values, is evaluated. Results of this study indicated that the Cl– concentration of the water and the chemical structure of the substances is more important than the pH of the water. There was no AOX at the beginning of the experiments, but a de-novo synthesis of AOX was observed during the batch experiments. This is caused by the high chloride content of the wastewaters. It can be supposed that OHradicals oxidize some chloride-ions to form chlorine, which further reacts with organic compounds. During the treatment, these AOX compounds which are produced from the beginning of the reaction are destroyed again. Evaluations of these experiments were done according to TOC and AOX results. Approximately 80% and 99% TOC removal efficiencies were obtained for the treatment of Phenol and Methanol-containing wastewaters, respectively. Objective In the literature, there are no relevant publications concerning the AOX formation of wastewater by wet oxidation- iron catalysed or by application of UV. For that reason, the main objectives of this study were: 1. to see the influence of chloride concentration and pH on the AOXde-novo formation with newly developed UV-Free Surface Reactor (UV-FSR), 2. to make a comparison of different AOPs, 3. to observe the effect of the chloride concentration on the TOC degradation efficiency, 4. to optimise reaction conditions. Methods In synthetic wastewaters, Methanol (CH3OH) and Phenol (C6H5 OH) are used as pollutants. The concentration of each substance was 1000 mg/l and COD values were calculated theoretically. The H2O2 addition was calculated according to the COD with a convenient stoichiometric factor (e.g. 1). During experiments, the pH was always kept constant with the addition of either 25% H2SO4 or 33% NaOH depending on the experimental conditions. Each substance was treated with the addition of 1000 mg/l Cl–, 10000 mg/l Cl– and without Cl– addition at pH 3, pH 7 and pH 10, respectively. NaCl was used as a Cl– source. Adsorbable Organic Halogenides (AOX) were determined using a TOX analyser (European Standard EN 1485 H 14, 1996). TOC measurements were carried out using an Elementar High TOC Analyzer equipped with an auto sampler. The H2O2 concentration was measured according to German Standard Methods (DIN 38409, Part 15, 1987). Results and Discussion The first step was to determine the effect of pH on the AOX formation in the process. Therefore, experiments were carried out at three different pHs: acidic (pH 3), neutral (pH 7) and basic (pH 10) conditions at a constant initial Methanol concentration of 1000 mg/l and a hydrogen peroxide concentration of 3185 mg/l (1 x stoichiometric). All results were evaluated according to applied pH. At these conditions, the amount of H2O2 (53 ml / 10 l) concentration was nearly zero after 1 hour batch treatment of Methanol. There was no AOX at the beginning of the experiments, but the AOX value increased after 6–18 min. At the end of 1 hour batch treatment this produced AOX was treated again. The maximum AOX production was obtained with the addition of 10000 mg/l Cl–, whereas there is no AOX production during the experiment when Cl– was not used. In all studies, however, TOC values decreased to almost zero after 1 hour batch treatment. After the experiments with Methanol, Phenol treatment was carried out at different pHs as a second experiment. pH was kept constant with the addition of either H2SO4 or NaOH depending on the experimental conditions. During experiments with Phenol, the colour of the water changed from colourless to a yellowish- red. After 1 hour treatment, the colour of the water was red. Therefore, these experiments were continued until the water became colourless again, and this took about 5 hours. Although there was no AOX at the beginning of the experiments, it increased after 30 min to 1 hour oxidation with the addition of 1000 mg/l Cl– and 10000 mg/l Cl–. There was no AOX production during the experiments when Cl– was not added. At the end of 5 hours of treatment, formed AOX was degraded and the TOC concentration decreased from 766 mg/l to approximately 200 mg/l. Conclusion. These experiments of this study showed that the effects of Cl– concentration of the water and the chemical structure of the substances is more than that of the pH on the AOX formation. During the batch experiments, a de-novo synthesis of AOX was observed very impressively due to the high chloride content of the wastewaters. It can be implied that OH-radicals oxidize some chloride-ions to form chlorine, which further reacts with organic compounds so that AOXde-novo is formed. At the end of the reaction times these AOX compounds are also destroyed. Recommendation and Outlook It is more cost effective to use these processes for only purposes such as toxicity reduction, enhancement of biodegradability, decolourisation and removal of micropollutants. However, the most important point is the optimization of the reaction conditions for the process of concern. The AOP applied can be used, for instance, for AOX reduction and TOC removal of industrial wastewaters.     

Remote sensing of the environment

A short survey of application areas and selection criteria for the different remote-sensing methods is presented. Microwave sensing is still regarded as one of the more progressive methods and its problem of angular resolution and the principle of synthetic-aperture radar are discussed. Experimental results of microwave probing are presented with examples from agriculture, meteorology, and hydrology.     

Untersuchungen über die Aufnahme organischer Substanzen durch die Wurzeln höherer Pflanzen. III. Alkaloide

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