Abstract:The rates of mineralization of phenol, benzoate, benzylamine,
p
-nitrophenol, and di(2-ethylhexyl) phthalate added to lake water at concentrations ranging from a few picograms to nanograms per milliliter were directly proportional to chemical concentration. The rates were still linear at levels of <1 pg of phenol or
p
-nitrophenol per ml, but it was less than the predicted value at 1.53 pg of 2,4-dichlorophenoxyacetate per ml. Mineralization of 2,4-dichlorophe… Show more
“…This limitation was due to the inherent limit in microbial competence in dechlorinating congeners with certain Cl substitution patterns [2,10]. It is unclear whether this limit is also affected by PCB concentrations, because the microbial population or activity is often determined by substrate concentrations [11][12][13][14].…”
Abstract-Dechlorination kinetics of polychlorinated biphenyls (PCBs) were investigated in Aroclor 1248-spiked sediments at 16 concentrations ranging from 0 to 200 ppm using sediment microorganisms from the Reynolds site in the St. Lawrence River, New York, USA, over a 58-week incubation period. The time course of dechlorination, measured as the total Cl per biphenyl, consisted of an initial lag phase followed by rapid dechlorination and then a plateau that represented an apparent endpoint of dechlorination. A clear threshold concentration was found between 35 and 45 ppm; there was no dechlorination observed at seven concentrations below this level. Above the threshold concentration, dechlorination rate was a function of sediment PCB concentration. The rate, calculated as the slope of the rapid phase, was linear within the concentration range investigated. The maximum extent of dechlorination also increased with initial Aroclor concentrations; only 4% of Cl per biphenyl was removed at 45 ppm, and the removal was saturated at approximately 36% above 125 ppm. This difference appeared to be due to whether or not dechlorination involved meta-rich congeners such as 25-2Ј (IUPAC no. 18), 25-2Ј5Ј-(no. 52), and 23-2Ј5Ј chlorobiphenyl (no. 44). These results indicate that a major controlling factor for natural remediation potential in sediments is the initial PCB concentration that determines the maximum extent of dechlorination rather than the dechlorination rate.
“…This limitation was due to the inherent limit in microbial competence in dechlorinating congeners with certain Cl substitution patterns [2,10]. It is unclear whether this limit is also affected by PCB concentrations, because the microbial population or activity is often determined by substrate concentrations [11][12][13][14].…”
Abstract-Dechlorination kinetics of polychlorinated biphenyls (PCBs) were investigated in Aroclor 1248-spiked sediments at 16 concentrations ranging from 0 to 200 ppm using sediment microorganisms from the Reynolds site in the St. Lawrence River, New York, USA, over a 58-week incubation period. The time course of dechlorination, measured as the total Cl per biphenyl, consisted of an initial lag phase followed by rapid dechlorination and then a plateau that represented an apparent endpoint of dechlorination. A clear threshold concentration was found between 35 and 45 ppm; there was no dechlorination observed at seven concentrations below this level. Above the threshold concentration, dechlorination rate was a function of sediment PCB concentration. The rate, calculated as the slope of the rapid phase, was linear within the concentration range investigated. The maximum extent of dechlorination also increased with initial Aroclor concentrations; only 4% of Cl per biphenyl was removed at 45 ppm, and the removal was saturated at approximately 36% above 125 ppm. This difference appeared to be due to whether or not dechlorination involved meta-rich congeners such as 25-2Ј (IUPAC no. 18), 25-2Ј5Ј-(no. 52), and 23-2Ј5Ј chlorobiphenyl (no. 44). These results indicate that a major controlling factor for natural remediation potential in sediments is the initial PCB concentration that determines the maximum extent of dechlorination rather than the dechlorination rate.
“…One obstacle in quantitative studies using I4C-labeled substances is how to define a rate constant from the nonlinear plots. The maximum rate (Boethling and Alexander, 1979) or the rate from the initial linear portion of the plots (Novick and Alexander, 1985;Rubin et al, 1982;Subba-Rao et al, 1982) have been used, and these rates were linear functions of co at low values of co with different chemicals under various conditions. The rate thus defined is probably equivalent to the rate constant k3, since the rate and the rate constant for a zero-order process are equivalent, and since k3 was also linear with low co.…”
The validity of the equation for first-order kinetics and of the empirical equation c = cok P 2 was checked against experimental data on the decomposition of the herbicides linuron and atrazine at different initial concentrations co, in soil. Standard statistical criteria showed acceptable fits to the data according to first-order kinetics, but the more stringent criterion of independence of the first-order rate constant on co proved this kinetics to be invalid. The empirical equation gave a better fit to the data. Furthermore, the rate constant k varied linearly with cg at low co and with c t z at high co. Similar relations between k and co were also found with 14C-labeled linuron, when it was found that the curve describing the collected amount of 14C in COz consisted of more than one phase. "he empirical equation can thus be used to assess quantitatively the influence of various factors on the degradation, using both unlabeled and 14C-labeled substances.
“…However, situations are known in which mineralization of a cosubstrate occurs. For example, Rubin et al [6] found that 95% of the radioactive carbon in labeled benzoic acid and phenylacetic acid that was added in low concentrations to samples of lake water or sewage was released as 14C02. Thus, a mineralization process similar to cometabolism may occur at low substrate concentrations.…”
Section: Modes Of Biodegradationmentioning
confidence: 99%
“…Obligate oligotrophs cannot tolerate high carbon concentrations, whereas facultative oligotrophs are dormant under conditions of high carbon concentrations but are reactivated when the carbon level is reduced. In contrast, eutrophs are organisms that proliferate under conditions of high organic carbon but do not function at low organic carbon concentrations [6,7]. Thus, a chemical present at high concentrations would tend to be degraded by eutrophs but would be unaffected by oligotrophs.…”
Section: Modes Of Biodegradationmentioning
confidence: 99%
“…Thus, it seems highly unlikely that results from these tests will provide good insight into the behavior of chemicals at trace concentrations in oligotrophic systems. For example, Rubin et al [6] reported that 2,4-D and di(2-ethylhexyl) phthalate (DEHP) did not --…”
Biodegradability testing is examined and the many factors affecting extrapolation of laboratory biodegradation results to microbial degradation in the environment are discussed. Recent advances in the understanding of the effects of the concentration and nature of various nutrients and organic substrates and modeling the microbial kinetics of degradation are reviewed. The advantages and disadvantages of screening methods and grab sample testing are discussed. The importance of groundwater biodegradation is also examined. Research needs are identified and guidelines are given to select various testing procedures to model diverse environmental situations.
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