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pH, Redox, and oxygen microprofiles in rhizosphere of bulrush (Scirpus validus) in a constructed wetland treating municipal wastewater.

Microenvironmental studies regarding plant oxygen release in a wastewater environment are important to understand the principles of constructed wetlands for wastewater treatment. pH, oxidation reduction potential (ORP), and dissolved oxygen (DO) microprofiles for the lateral and main roots of the bulrush (Scirpus validus) in a vertical flow constructed wetland fed with municipal wastewater were measured using microelectrode techniques. pH was found to be low (6.91-6.98) near the lateral root surface, indicating possible nitrification or H(+) extrusion. The ORP at the lateral root surface was between +250 and +317 mV and gradually reached the bulk solution ORP (+14 to -54 mV) at a radial distance of approximately 4,750 microm. DO values at the lateral root surface varied from 0.64-2.04 mg L(-1) as bulk biochemical oxygen demand (BOD) changed from 24 to 1,267 mg L(-1). DO at the lateral root surface and the thickness of the oxygen layer around the root marginally increased with an increase in bulk BOD, while ORP at the lateral and main root surface decreased. pH and DO values did not change near the main root and had the bulk solution values. The results of this study provide insights into root-induced microenvironments and would be helpful for the quantification of the total amount of oxygen contributed by plants in constructed wetlands.

Biodegradation, Environmental↗

Increased solubility of (heavy) metals in soil during microbial transformations of sucrose and casein amendments.

Unsterile soil samples pH 6.8 were amended with 10% sucrose or 0.1% NH4NO3/2% casein to influence solubility of metal cations. Microbial formation of aliphatic carboxylic acids reduced pH of sucrose soil to 4.3 and increased the solubility of heavy metals by 60-fold due to the increased presence of H+, and the metal-chelating and humic-molecule fragmenting properties of carboxylic acids. Soil pH increased finally to 7.8 upon the degradation of the carboxylic acids. In casein soil, ammonia production increased pH initially to 8.5 and promoted solubility of metal-containing humic compounds. Subsequent nitrification reduced pH to 5.6 to increase concentations of Ca and Mg in the soil solution, which prevented a comparable increase in the solubility of heavy metals competitively. It is concluded that amendment with sugar and nitrogen occasionally increases the concentrations of (hazardous) elements in the soil solution to facilitate their uptake by metal hyperaccumulating plants.

Bacteria↗

Factors influencing water solubility and plant availability of mineral compounds in the tripartite fairy rings of Marasmius oreades (BOLT.: FR.) FR.

Fairy rings of M. oreades on pasture land were denoted by the dark-green vegetation. Grasses and rooted soils were analyzed to determine the influence of nonsymbiotic fungal mats on plant uptake of (heavy) metals. In soil colonized by M. oreades, degradation of 20-35% of plant roots in the presence of fungal laccase increased the content of dissolved organic carbon (3.74x), hexose sugar (3.75x), NH(3)/NH(4) (+) (5.1x), NO(3) (-) (11.1x), the number of aerobic bacteria (14.4x), and the formation of the phytochelators, oxalic, citric, and malonic acids. Soil pH diminished by 1.5 units mainly due to nitrification and carboxylic acid production. Although the solubility of trace elements increased (6.1x), plant roots had the same trace metal content as control plants, whereas the shoot content in Al, Cr, Fe, Ni, and Ti decreased by more than 50% due to inhibited root-to-shoot transfer. It is concluded that M. oreades and its associated bacteria increase the solubility of soil minerals significantly, but make them, due to presumed particularities in their complexation, less plant available and less re-complexable for the translocation into the plant vascular system.

Agaricales↗

Nitrogen isotopomer site preference of N2O produced by Nitrosomonas europaea and Methylococcus capsulatus Bath.

The relative importance of individual microbial pathways in nitrous oxide (N(2)O) production is not well known. The intramolecular distribution of (15)N in N(2)O provides a basis for distinguishing biological pathways. Concentrated cell suspensions of Methylococcus capsulatus Bath and Nitrosomonas europaea were used to investigate the site preference of N(2)O by microbial processes during nitrification. The average site preference of N(2)O formed during hydroxylamine oxidation by M. capsulatus Bath (5.5 +/- 3.5 per thousand) and N. europaea (-2.3 +/- 1.9 per thousand) and nitrite reduction by N. europaea (-8.3 +/- 3.6 per thousand) differed significantly (ANOVA, f((2,35)) = 247.9, p = 0). These results demonstrate that the mechanisms for hydroxylamine oxidation are distinct in M. capsulatus Bath and N. europaea. The average delta(18)O-N(2)O values of N(2)O formed during hydroxylamine oxidation for M. capsulatus Bath (53.1 +/- 2.9 per thousand) and N. europaea (-23.4 +/- 7.2 per thousand) and nitrite reduction by N. europaea (4.6 +/- 1.4 per thousand) were significantly different (ANOVA, f((2,35)) = 279.98, p = 0). Although the nitrogen isotope value of the substrate, hydroxylamine, was similar in both cultures, the observed fractionation (delta(15)N) associated with N(2)O production via hydroxylamine oxidation by M. capsulatus Bath and N. europaea (-2.3 and 26.0 per thousand, respectively) provided evidence that differences in isotopic fractionation were associated with these two organisms. The site preferences in this study are the first measured values for isolated microbial processes. The differences in site preference are significant and indicate that isotopomers provide a basis for apportioning biological processes producing N(2)O.

Binding Sites↗

Effects of the herbicide hexazinone on nutrient cycling in a low-pH blueberry soil.

The herbicide hexazinone was applied as the commercial formulation Velpar L at field-rate (FR) concentrations of FR (14.77 microg ai g(-1)), FRx5 (73.85 microg ai g(-1)), FRx10 (147.70 microg ai g(-1)), FRx50 (738.50 microg ai g(-1)), and FRx100 (1477.00 microg ai g(-1)) to acidic soil, pH 4.12, taken from a lowbush blueberry field. Hexazinone was tested for inhibitory effects on various transformations of the nitrogen cycle and soil respiration. Nitrogen fixation was unaffected by hexazinone levels up to FRx100 following a 4-week incubation period. Ammonification was initially inhibited by all levels of hexazinone, but after 4 weeks, ammonification in all treatment systems was equal to or greater than the control. Nitrification was more sensitive to hexazinone; however, application at a field-rate level caused no inhibition. Inhibitory effects were noted above FR after a 2-month endpoint analysis and above FRx5 after a 6-month endpoint analysis. Hexazinone concentrations up to and including FRx100 stimulated denitrification. Soil respiration was also stimulated over a 3-week period when applied at a level up to 100 times the recommended field rate. In general, it was found that when applied at the recommended field application rate, hexazinone does not adversely affect the nitrogen cycle or soil respiration in acidic lowbush blueberry soils.

Agriculture↗

Microbial sensors on a respiratory basis for wastewater monitoring.

In respect of their rapidity, their online capabilities, and their moderate costs, biosensing systems generally offer an attractive alternative to the existing methods of water analysis. Additionally, one particular advantage of microbial biosensors is the ability to measure direct effects on living cells, e.g., their respiratory activity and its alteration caused by environmental pollutants. It is true that microbial sensors, often do not provide the optimum solution for the determination of individual analytes when compared to established physico-chemical analysis methods. However, these biosensing devices are predestined for the summary determination of environmentally relevant compounds and their complex effects, respectively. For this reason, microbial sensors allow an integral evaluation of the degree of environmental pollution including the interaction of various compounds. Moreover, in some cases specific metabolic pathways in microorganisms are used, resulting in the development of microbial sensors for the more selective analysis for those compounds or pollutants, which cannot be measured by simple enzyme reactions, e.g., the determination of aromatic compounds and heavy metals. This chapter gives an overview of microbiological biosensors on respiratory basis for the measurement of the following environmentally relevant compounds: inorganic N-compounds, heavy metals, organic xenobiotics and the estimation of sum parameters or so-called complex parameters such as BOD, ADOC, N-BOD, and the inhibition of nitrification.

Bacteria↗

Bacterial and enzymatic bioassays for toxicity testing in the environment.

Microbioassays using bacteria or enzymes are increasingly applied to measure chemical toxicity in the environment. Attractive features of these assays may include low cost, rapid response to toxicants, high sample throughput, modest laboratory equipment and space requirements, low sample volume, portability, and reproducible responses. Enzymatic tests rely on measurement of either enzyme activity or enzyme biosynthesis. Dehydrogenases are the enzymes most used in toxicity testing. Assay of dehydrogenase activity is conveniently carried out using oxidoreduction dyes such as tetrazolium salts. Other enzyme activity tests utilize ATPases, esterases, phosphatases, urease, luciferase, beta-galactosidase, protease, amylase, or beta-glucosidase. Recently, the inhibition of enzyme (beta-galactosidase, tryptophanase, alpha-glucosidase) biosynthesis has been explored as a basis for toxicity testing. Enzyme biosynthesis was found to be generally more sensitive to organic chemicals than enzyme activity. Bacterial toxicity tests are based on bioluminescence, motility, growth, viability, ATP, oxygen uptake, nitrification, or heat production. An important aspect of bacterial tests is the permeability of cells to environmental toxicants, particularly organic chemicals of hydrophobic nature. Physical, chemical, and genetic alterations of the outer membrane of E. coli have been found to affect test sensitivity to organic toxicants. Several microbioassays are now commercially available. The names of the assays and their basis are: Microtox (bioluminescence), Polytox (respiration), ECHA Biocide Monitor (dehydrogenase activity), Toxi-Chromotest (enzyme biosynthesis), and MetPAD (enzyme activity). An important feature common to these tests is the provision of standardized cultures of bacteria in freeze-dried form. Two of the more recent applications of microbioassays are in sediment toxicity testing and toxicity reduction evaluation. Sediment pore water may be assayed directly or solvents may be used to extract the toxicants. Some of the solvents used for extraction of organic chemicals are themselves toxic to bacteria (e.g., dichloromethane), requiring exchange with a less toxic solvent (e.g., ethanol, methanol, DMSO). A modification of the Microtox test allows direct assay of solid-phase samples such as sediments. The toxicity reduction evaluation (TRE) must be carried out at wastewater treatment plants whose effluents fail toxicity standards. The TREs require numerous and repeated toxicity assays, thus favoring application of microbioassays. Presently, no single microbioassay can detect all categories of environmental toxicants with equal sensitivity. Therefore, a battery of tests approach is recommended. The differential sensitivity of alternative tests may, in fact, be exploited. Further research is needed to construct strains of genetically engineered microorganisms or isolate microorganisms or enzymes that respond to specific classes of toxicants. These can be combined into batteries appropriate for different environments or test objectives.

Bacteria↗

Biotreatment of ammonia- and butanal-containing waste gases.

The biological removal of ammonia and butanal in contaminated air was investigated by using, respectively, a laboratory-scale filter and a scrubber-filter combination. It was shown that ammonia can be removed with an elimination efficiency of 83% at a volumetric load of 100 m3.m-2.h-1 with 4-16 ppm of ammonia. During the experiment percolates were analysed for nitrate, nitrite, ammonium and pH. It was found that the nitrification in the biofilter could deteriorate due to an inhibition of Nitrobacter species, when the free ammonia concentration was rising in the percolate. It should be easy to control such inhibition through periodic analysis of the liquid phase by using a filter-scrubber combination. Such a combination was studied for butanal removal. Butanal was removed with an elimination efficiency of 80% by a scrubber-filter combination at a volumetric load of 100 m3.m-2.h-1 and a high butanal input concentration. Mixing the filter material with CaCO3 and pH control of the liquid in the scrubber resulted in an increase of the elimination efficiency. These results, combined with previous results on the biofiltration of butanal and butyric acid, allow us to discuss the influence of odour compounds on the removal efficiency of such systems and methods for control. The results were used to construct a full-size system, which is described.

Air Pollutants↗

Adenine nucleotide pool variations in intact Nitrobacter winogradskyi cells.

1. The ATP pool in Nitrobacter winogradskyi cells was determined by means of the luciferin-luciferase enzyme system and the ADP and AMP pools were measured after enzymatic conversion into ATP. 2. In the first 10 min after addition of nitrite to endogenously respiring cells, which had stood for 5--16 days after completion of the nitrite oxidation, the ATP pool dropped about 60%. 3. During the log phase the ATP pool was approx. 20--40 pmoles/5 mug cell-N. During growth it increased exponentially by 3--4 times the amount until the nitrite had been used up. Subsquently the ATP pool decreased at first rapidly and then more slowly without sinking to 0 in the first 2 months after nitrification. 4. Nitrite oxidizing cells had an energy charge of 0.37 during the log-phase. After approx. 90% of the substrate had been used up the energy charge had reached 0.57. 5. If the CO2 assimilation was inhibited in growing cultures by increased oxygen partial pressure, nitrite oxidation continued but the ATP pool increased. 6. The ATP pool and the activity of the endogenous respiration decreased by more than 50% during the first hours after the substrate had been used up.

Adenine Nucleotides↗

Aerobic denitrification in various heterotrophic nitrifiers.

Various heterotrophic nitrifiers have been tested and found to also be aerobic denitrifiers. The simultaneous use of two electron acceptors (oxygen and nitrate) permits these organisms to grow more rapidly than on either single electron acceptor, but generally results in a lower yield than is obtained on oxygen, alone. One strain, formerly known as "Pseudomonas denitrificans", was grown in the chemostat and shown to achieve nitrification rates of up to 44 nmol NH3 min-1 mg protein-1 and denitrification rates up to 69 nmol NO3(-1) min-1 mg protein-1. Unlike Thiosphaera pantotropha, this strain needed to induce its nitrate reductase. However, the remainder of the denitrifying pathway was constitutive and, like T. pantotropha, "Ps. denitrificans" probably possesses the copper nitrite reductase.

Aerobiosis↗

Growth of Nitrobacter in the presence of organic matter. I. Mixotrophic growth.

1. Culture filtrates of heterotrophic bacteria were tested for their stimulatory effect on nitrification of three strains of Nitrobacter. 2. Yeast extract-peptone solution, in which Pseudomonas fluorescens had grown, after removal of the cells was added to autotrophically growing cultures of Nitrobacter agilis; it caused a stimulated nitrite oxidation and growth of Nitrobacter agilis. 3. The degree of stimulation depended on: a) the proportion of the culture filtrate to the autotrophic medium; b) the composition of the complex medium in which Pseudomonas fluorescens had been grown; c) the time the heterotrophic bacterium had been grown in the complex medium. 4. The stimulatory effect was highest with Nitrobacter agilis, less with Nitrobacter winogradskyi and negligible with Nitrobacter K4. 5. It was possible to adapt nutrifying cells of Nitrobacter agilis to higher concentrations of yeast extract and peptone. After the nitrite had been completely oxidized the cell-N still increased up to 30% before growth stopped.

Culture Media↗

The influence of anaerobic pretreatment on the nitrogen removal from biosynthetic pharmaceutical wastewaters.

The C:N ratio of the pharmaceutical wastewaters is usually suitable for a combination of the anaerobic pretreatment with the high COD removal and aerobic posttreatment with the efficient biological N removal. This kind of anaerobic-aerobic process was tested in semipilot scale by using a UASB reactor and an activated sludge system with a predenitrification (total volume 100 l). It was found that at a total HRT of 2.3 days an average of 97.5% of COD and 73.5% of total N was removed. The UASB reactor was operated at 30 degrees C with a volumetric loading rate of 8.7 kg.m-3.d-1, the efficiency of COD removal was 92.2%. The processes, which take part in the biological removal of nitrogen, especially the nitrification, were running with lower rates than usually observed in aerobic treatment systems.

Aerobiosis↗

Simultaneous NH3 oxidation and N2 production at reduced O2 tensions by sewage sludge subcultured with chemolithotrophic medium.

The ammonia oxidation rate by sewage sludge was determined as a function of the dissolved oxygen tension. Samples of sludge were taken from a domestic waste water treatment pilot plant in which sludge was completely retained by membrane filtration. The samples were subcultured chemolithotrophically in recycling reactors. The gas supplied was a mixture of pure argon and oxygen. The KO2 for ammonia oxidation was estimated to be 0.97 (+/- 0.16) kPa dissolved oxygen. Together with ammonia oxidation and oxygen consumption, dinitrogen gas was produced. So, aerobic denitrification occurred. At dissolved oxygen tensions of 1.25 kPa and higher, the dinitrogen production rate (per N-mole) equalled 20% of the ammonia oxidation rate. This proportion was even 58% at 0.3 kPa dissolved oxygen. At 0.15 kPa dissolved oxygen, however, nitrification hardly proceeded, while dinitrogen production soon stopped. Most likely, a nitrifier concomitantly oxidized ammonia and reduced nitrite to dinitrogen.

Ammonia↗

Stoichiometry and kinetics of microbial toluene degradation under denitrifying conditions.

Batch experiments were carried out to investigate the stoichiometry and kinetics of microbial degradation of toluene under denitrifying conditions. The inoculum originated from a mixture of sludges from sewage treatment plants with alternating nitrification and denitrification. The culture was able to degrade toluene under anaerobic conditions in the presence of nitrate, nitrite, nitric oxide, or nitrous oxide. No degradation occurred in the absence of Noxides. The culture was also able to use oxygen, but ferric iron could not be used as an electron acceptor. In experiments with 14C-labeled toluene, 34% +/- 8% of the carbon was incorporated into the biomass, while 53% +/- 10% was recovered as 14CO2, and 6% +/- 2% remained in the medium as nonvolatile water soluble products. The average consumption of nitrate in experiments, where all the reduced nitrate was recovered as nitrite, was 1.3 +/- 0.2 mg of nitrate-N per mg of toluene. This nitrate reduction accounted for 70% of the electrons donated during the oxidation of toluene. When nitrate was reduced to nitrogen gas, the consumption was 0.7 +/- 0.2 mg per mg of toluene, accounting for 97% of the donated electrons. Since the ammonia concentration decreased during degradation, dissimilatory reduction of nitrate to ammonia was not the reductive process. The degradation of toluene was modelled by classical Monod kinetics. The maximum specific rate of degradation, k, was estimated to be 0.71 mg toluene per mg of protein per hour, and the Monod saturation constant, Ks, to be 0.2 mg toluene/l. The maximum specific growth rate, mu max, was estimated to be 0.1 per hour, and the yield coefficient, Y, was 0.14 mg protein per mg toluene.

Bacteria, Anaerobic↗

Chlorflurenol-methyl in soil: degradation, leaching, and effects on microbiological processes.

Tests were conducted with the synthetic growth regulator chlorflurenol-methyl to investigate its rate of degradation in soil, leaching behavior, and possible side-effects on the soil microflora and on soil physiological processes. With two sandy soils (Ct = 1.0 and 2.58%) which were treated with 11.35 mg kg-1 chlorflurenol-methyl (congruent to 2.8 kg a.i. ha-1), over 90% of the compound disappeared within 4 to 8 days. The degradation products were 2-chloro-9-hydroxyfluorene-9-carboxylic acid and 2-chlorofluorenone, which undergo further decomposition. In leaching tests with three sandy soils (Ct = 0.69, 1.0 and 2.58%), chlorflurenol-methyl was not washed from the soil; however, with one soil (0.69% C), very small residues were observed in the effluent identified as 2-chlorofluorenone. In side-effects experiments with a parabrown (Ct = 1.26%) and a chernozem soil (Ct = 2.3%), which were treated with 1 and 10 mg kg-1 chlorflurenolmethyl, no persistent inhibition of anaerobic or aerobic nitrogen fixation (C2H2-reduction) was detected. Ammonification, nitrification, and mineralization of soluble starch were also not influenced. The mineralization of cellulose in compost soil (Ct = 13.59%) was temporarily delayed; however, this delay was later compensated for by a higher mineralization rate. The colonization density of fungi on soil particles and the numbers of bacteria, actinomycetes, and fungi were not negatively influenced. Chlorflurenol-methyl does not significantly influence these microbiological processes and populations in the soil.

Actinomycetales↗

Effects of pesticides on soil microflora using dalapon as an example.

Effects of the herbicide dalapon on the soil microflora are evaluated. Measurements were made on populations and pure cultures of micro-organisms, dehydrogenase and phosphatase, soil respiration, and nitrogen transformations. At normal concentrations of 2.6 and 26 ppm, dalapon had little effect and is unlikely to harm the soil microflora or soil fertility. At abnormal concentrations of 266 and 2,660 ppm, marked effects occurred on the microflora and its activities. In one soil, 2,660 ppm dalapon significantly increased production of ammonium-nitrogen; nitrification was almost totally inhibited in this soil. The results are discussed in terms of the validity of the tests for detecting effects of pesticides on the soil microflora. Some problems, particularly of data interpretation and evaluation, are high-lighted.

Bacteria↗

Issues, Impacts, and Implications of Shrimp Aquaculture in Thailand

Water quality impacts to and from intensive shrimp aquaculture in Thailand are substantial. Besides the surface and subsurface salinization of freshwaters, loadings of solids, oxygen-consuming organic matter, and nutrients to receiving waters are considerable when the cumulative impacts from water exchange during the growout cycle, pond drainage during harvesting, and illegal pond sediment disposal are taken into account. Although just beginning to be considered in Thailand, partial recirculating and integrated intensive farming systems are producing promising, if somewhat limited, results. By providing on-site treatment of the effluent from the shrimp growout ponds, there is less reliance on using outside water supplies, believed to be the source of the contamination.The explosion in the number of intensively operated shrimp farms has not only impacted the coastal zone of Thailand, but has also resulted in an unsustainable aquaculture industry. Abandonment of shrimp ponds due to either drastic, disease-caused collapses or more grandual, year-to-year reductions in the productivity of the pond is common. To move Thailand towards a more sustainable aquaculture industry and coastal zone environment, integrated aquaculture management is needed. Components of integrated aquaculture management are technical and institutional. The technical components involve deployment of wastewater treatment and minimal water-use systems aimed at making aquaculture operations more hydraulically closed. Before this is possible, technical and economic feasibility studies on enhanced nitrification systems and organic solids removal by oxidation between production cycles and/or the utilization of plastic pond liners need to be conducted. The integration of semi-intensive aquaculture within mangrove areas also should be investigated since mangrove losses attributable to shrimp aquaculture are estimated to be between 16 and 32 % of the total mangrove area destroyed betweeen 1979 and 1993.Government policy needs to devote as much attention to sustainability issues as it has on promoting intensive pond culture. Such a balanced policy would include training and education monitoring and enforcement, rehabilitating abandoned ponds, managing land use within the coastal zone, more community involvement, and government reorganization to eliminate overlapping jurisdictions among agencies.As integrated aquaculture management becomes more the practice than the exception, less risk of crop failure to the industry and reduced discharge loadings from intensively managed shrimp ponds to receiving waters can be expected. Projected limitations on growing and marketing shrimp in the future, such as scarcity of land and broodstock, continued disease outbreaks, negative publicity, regulatory enforcement, water treatment and solids disposal costs, and increased competition from growers in other Asian countries will also drive the government and the industry towards adopting integrated aquaculture management.KEY WORDS: Shrimp aquaculture; Thailand; Historical practices; Environmental impacts; Sustainability; Integrated management; Water treatment; Institutional aspects

Journal Article↗

Measurement and prediction of the disappearance rates from soil of 6-chloropicolinic acid.

6-Chloropicolinic acid is the sole detectable metabolite, other than carbon dioxide, arising from decomposition of 2-chloro-6-(trichloromethyl) pyridine in soil. The pyridine compound is a potent inhibitor of nitrification now in use with ammonium fertilizers. The purpose of this study was to evaluate the relative influence of various soil and climatic factors on rates of degradation of 6-chloropicolinic acid in soil. Experiments with a wide range of soil types (23 soils) demonstrate that the most important factor influencing the decomposition rate of 6-chloropicolinic acid is soil temperature. When temperature is not a variable, the quantity of organic matter (0.9 to 6.9% by weight) and pH (4.8 to 8.1) significantly affect the rate of decomposition, but sand, silt, and clay percentages do not. Moisture content was without apparent effect because the range of values investigated was too narrow. A fractional-order rate law (0.7) describes the disappearance rate best. Application of the Arrhenius equation to the data for the decomposition of 6-chloropicolinic acid in soil indicates an activation energy of 6.57 kcal per mole, suggesting that the chemical is biologically rather than chemically degraded. It was not possible to develop a suitably precise equation for prediction of loss rate as affected by the above soil and climatic factors because undefined biological factors in the soils override the effect of measurable properties of soil and climate.

Biodegradation, Environmental↗