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Shortcomings of the laboratory-derived median lethal concentration for predicting mortality in field populations: exposure duration and latent mortality.

Exposure duration and intensity (concentration or dose) determine lethal effects of toxicants. However, environmental regulators have focused on exposure intensity and have considered duration only peripherally. Conventional testing for toxicology tends to fix exposure time and to use the median lethal concentration (LC50) at that time to quantify mortality. Fixing the exposure duration and selecting the 50% mortality level for reasons of statistical and logistical convenience result in the loss of ecologically relevant information generated at all other times and ignore latent mortality that manifests after the exposure ends. In the present study, we used survival analysis, which is widely employed in other fields, to include both time and concentration as covariates and to quantify latent mortality. This was done with two contrasting toxicants, copper sulfate (CuSO4) and sodium pentachlorophenol (NaPCP). Amphipods (Hyalella azteca) were exposed to different toxicant concentrations, and the percentage mortalities were noted both during and after the exposure ended. For CuSO4 at the conventional 48-h LC50 concentrations, the predicted proportions dead after including latent mortality were 65 to 85%, not 50%. In contrast, only 5% or fewer additional animals died if the latent mortality was included for NaPCP. The data (including exposure time, concentration, and proportion dead at each time) for each toxicant were then successfully fit with survival models. The proportion of organisms dying at any combination of exposure concentration and time can be predicted from such models. Survival models including latent mortality produced predictions of lethal effects that were more meaningful in an ecological or field context than those from conventional LC50 methods.

Amphipoda↗

Sorption of hydrophobic organic chemicals to bacteria.

The toxicity and time-dependent sorption of three hydrophobic organic chemicals to Rhodococcus rhodochrous bacteria were investigated. In experiments, environmentally relevant concentrations of pentachlorophenol (PCP), hexachlorobenzene (HCB), and dichlorobiphenyl (DPCB) were applied to living (both growing and nongrowing) bacteria as well as to dead bacteria. For PCP (an ionizing chemical), bacterial growth decreased, and bacterial death increased, as the PCP concentration increased. In sorption experiments with PCP, the partition coefficient was affected by the active uptake of PCP by living but not by dead bacteria, by the death of the living bacteria because of PCP toxicity, and by saturation of site-specific sorption as the PCP concentration increased. Hexachlorobenzene (a nonionizing chemical) did not affect bacterial growth or death at all HCB concentrations investigated. In sorption experiments with HCB, the partition coefficient depended on the rate of bacterial growth relative to the sorption rate. The sorption rate depended on the state of bacterial aggregation, and this changed with time. Results for DPCB (a nonionizing chemical with an equilibrium partition coefficient similar to that of HCB) were similar to those for HCB.

Absorption↗

Body residues as dose for sublethal responses in alevins of landlocked salmon (Salmo salar m. sebago): a direct calorimetry study.

Questions of organism-specific factors, toxicity endpoints, and their relation to mode-of-action all are related to consistency and applicability of body residue-based approaches. To address this issue, direct calorimetry was used to evaluate metabolic responses of alevins of landlocked salmon (Salmo salar m. sebago) to pentachlorophenol (PCP) exposure ranging from 0 to 1.04 microM for 24 h or 24, 48, and 72 h (0, 0.26, and 0.55 microM, respectively). The body residues were used as a dose metric for sublethal responses. The body size, rapid ontogenetic development, and exposure to a specific pollutant all were heat output-modifying factors. The acute exposure (24-72 h) to PCP led to a heat output-enhancing effect, which directly was related to an internal concentration of PCP in the range of 0.01 to 0.15 micromol/g. Within the treatments, body size per level of metabolic rate and magnitude of physiological response were not correlated, thus the alevins with higher mass-specific metabolic rate were not more sensitive to PCP. Primarily, increasing metabolic rate during posthatch development controls PCP toxicity only by affecting bioaccumulation kinetics, not the toxic potency of the chemical. New information of a relationship between observed natural variation in measured physiological trait of fish and PCP-induced response and its body residue-based level is of ecotoxicological importance.

Animals↗

Application of biological activated carbon anaerobic reactor for treatment of hazardous chemicals.

An expanded-bed anaerobic reactor with granular activated carbon (GAC) medium has been developed to treat wastewaters that contain a high concentration of inhibitory and/or refractory organic compounds as well as readily degradable organic compounds. The process is characterised by a combination of two removal mechanisms; adsorption on GAC and biological degradation by microorganisms grown on GAC. Applicability of the reactor to treatment of phenol, chloroacetaldehyde (CAA), pentachlorophenol (PCP) and tetrachloroethylene (PCE) was discussed based on experimental data. All chemicals focused on here were removed well and stably at a removal efficiency of more than 98% even during starting operation and shock load operation. Chemicals in influent that exceeded biological degradation capacity was initially adsorbed on GAC and then gradually degraded, and hence the adsorptive capacity of GAC was regenerated biologically. These results proved that a biological activated carbon anaerobic reactor was effective for treatment of wastewater containing hazardous chemicals, especially for strongly absorbable chemicals, as well as readily degradable organic compounds at high concentration.

Acetaldehyde↗

Accident insurance, sickness, and science: New Zealand's no-fault system.

This article explores the process of seeking compensation for occupational illness under a no-fault accident insurance scheme. The author uses two case studies--firefighters who attended a fire at a chemical storage depot and timbermill workers who worked with pentachlorophenol--to illustrate how science can be used to deny compensation to sick and dying workers. The results of the studies suggest that a no-fault accident compensation scheme, considered to be a victory for workers, offers no guarantee of just outcomes for working people. And science can be co-opted and used to support business and state interests against workers; this ideological support is increasingly hidden behind the development of "objective" systems of assessing compensation claims.

Capitalism↗

The metabolism of phenol and substituted phenols in zebra fish.

1. The metabolism of five phenols in zebra fish was studied after uptake from the medium. The results showed no qualitative differences to other Cyprinid fish species, only the oxidation rate seemed to be lower. 2. Phenyl glucuronide, phenyl sulphate, and quinol sulphate were identified as metabolites of phenol. 3. Identified metabolites of 2-cresol were 2-cresyl glucuronide, 2-cresyl sulphate, and 2-hydroxybenzoic acid in trace amounts. 4. Only the glucuronide and sulphate conjugates were detected as metabolites of 4-nitrophenol, 4-chlorophenol, and pentachlorophenol.

Animals↗

The fate of 4-cyanoacetanilide in rats and mice; mechanism of formation of a novel electrophilic metabolite.

1. The metabolic fate of 4-cyanoacetanilide (CAA), labelled with 14C and 13C in the N-acetyl group, was studied in rats (oral dose, 22.5 mg/kg) and mice (oral dose 21.7 mg/kg). 2. The metabolic profile in the urine of rats was compared with that obtained previously with 4-cyano-N,N-dimethylaniline (CDA) and confirms the intermediacy of CAA in the metabolism of CDA. 3. The precursor of a major metabolite of CDA and CAA (the mercapturic acid N-acetyl-S-[2-keto-2-(4-cyanoanilino)ethyl]cysteine, metabolite C) was identified in the urine of CAA-dosed rats as the O-sulphate conjugate of N-(4-cyanophenyl)glycolamide. 4. Pretreatment of rats with the sulphotransferase inhibitor pentachlorophenol reduced the yield of the mercapturic acid metabolite C, further indicating the intermediacy of a sulphate conjugate. 5. Metabolite C was not formed from CAA by mice; thus, this species difference, also observed with CDA, occurs at the level side-chain (acetyl) hydroxylation as well as at N-acetylation of 4-cyanoaniline as previously proposed. 6. The significance of this pathway as a bioactivation reaction of CDA, CAA and other acetanilides is discussed.

Acetanilides↗

Toxicokinetics of pentachloroanisole in F344 rats and B6C3F1 mice.

1. Toxicokinetics of pentachloroanisole (PCA) were studied in F344 rat and B6C3F1 mouse of both sexes by gavage at doses of 10, 20 and 40 mg/kg and by i.v. at 10 mg/kg. 2. PCA was rapidly demethylated to pentachlorophenol (PCP) in both rat and mouse and the resulting PCP plasma concentrations were much higher than that of parent PCA due to the much smaller apparent volume of distribution of PCP. 3. Peak plasma concentrations of PCA and PCP increased with dose in both rat and mouse. 4. Bioavailability of PCA was low in both rat and mouse and was sex independent. 5. The high plasma concentrations and relatively long biological half-life of PCP in both species after both i.v. and oral dosing with PCA indicate possible bioaccumulation of PCP upon multiple oral administrations of PCA.

Animals↗

Regulation of arylsulfate sulfotransferase from a human intestinal bacterium by nucleotides and magnesium ion.

Arylsulfate sulfotransferase (ASST) from a human intestinal bacterium stoichiometrically catalyzed the transfer of a sulfate group from phenylsulfate esters to phenolic compounds. Pentachlorophenol, one of the selective inhibitors of phenol sulfoconjugation in mammalian tissues, inhibited both phenol and tyramine sulfation by ASST. Nucleotide triphosphates such as ATP, GTP, UTP and CTP, and pyrophosphate inhibited the ASST activity, whereas Mg2+ and Mn2+ activated the enzyme and prevented its inhibition by ATP and pyrophosphate. Equimolar binding of [alpha-] and [gamma-32P]ATP to the enzyme showed that the enzyme protein was not phosphorylated, but bound ATP. These results suggest that nucleotide triphosphates and divalent cations are important modulators in the control of ASST activity.

Adenosine Triphosphate↗

Effects of cholesterol feeding on the distribution, metabolism, and accumulation of pentachlorobenzene in rats.

To investigate the influence of cholesterol content in tissue on the distribution, metabolism, and accumulation of pentachlorobenzene (PECB), rats were fed on a cholesterol-enriched (CHE) diet or a basal diet for 4 weeks. At two weeks, a single dose or a 6-day dosage of PECB was orally administered. The serum cholesterol concentration in the CHE diet group was 2.1-2.9 times higher than that in the basal diet group, while the serum triglyceride concentration decreased. The serum lipid levels were similar to the levels at two weeks. The blood PECB concentration was not different between the two groups. Increases in the contents of PECB and lipid in tissue due to the CHE diet feeding were observed only in liver (PECB, 2.6-3.0 times; triglyceride, 2-3 times; cholesterol, 10-15 times). Content of pentachlorophenol, a main metabolite of PECB, and the level of drug-metabolizing enzymes in liver of the CHE diet group tended to be higher than those of the basal diet group. These results suggested that the increase in PECB accumulation in the liver of the CHE diet group was not due to the decrease of PECB metabolism but due to the increase in the content of cholesterol and triglyceride.

Animals↗

Feeding fish oil to rats accelerates the metabolism of hexachlorobenzene.

This study was conducted to examine the influence of dietary fat on the metabolism and excretion of hexachlorobenzene (HCB), a ubiquitous food contaminant which is metabolized at a low rate. Three groups of rats were fed semi-purified diets containing 10 g/100 g of either soybean oil, lard or fish oil for 2 wk and then given a single dose of HCB by intragastric gavage. The concentrations of HCB and pentachlorophenol (PCP), a major metabolite of HCB, were monitored in the blood for 5 d. Fecal excretion of HCB did not differ among the three groups, indicating no difference in HCB retained in the body among the groups. Concentrations of HCB in blood, liver and brain samples from the lard and fish oil groups, the members of which had a low fat tissue mass, were consistently higher as compared with those in samples from the soybean oil group. The concentration of PCP and the PCP/HCB ratio in the blood were higher in the fish oil group than in the other groups. In addition, the amount of PCP excreted in urine was highest in the fish oil group. The hepatic cytochrome P-450 content in the fish oil group was higher than that in the other groups. These findings indicate that feeding fish oil to rats accelerated HCB metabolism. An increase in hepatic HCB concentration due to a small fat tissue mass and high hepatic cytochrome P-450 content may have played a role in accelerating HCB metabolism in the fish oil group.

Adipose Tissue↗

[Inhibitory effect of green tea infusion of hepatotoxicity].

We first showed a drinking of green tea infusion can inhibit chemically induced possible hepatic tissue damages in animal experiments, although it has been shown that oral administration of green tea extract can inhibit some organ toxicities. In this review, our data are summarized and a possibility of the effectiveness in humans is discussed. Male rats or mice in the series of experiments were given 2% green tea infusion as a drinking water 1 or 2 weeks before the chemical treatment and until the termination. In the study of rats, green tea effectively inhibited the hepatotoxicity induced by a single intraperitoneal injection or by repeated gavage administration of 2-nitropropane, and a single intraperitoneal injection of galactosamine. However, any possible effects were not observed when green tea was given, on the hepatotoxicity by a single or repeated gavage administration of carbon tetrachloride. In the study of mice, green tea inhibited the hepatotoxicity induced by administration of pentachlorophenol in diet. In conclusion, 2% green tea infusion can prevent the hepatotoxicity by at least some chemicals in experimental animals. It is inferred that the amount of green tea taken by animals in this experiment might be equivalent to the daily intake in Japanese general population, by calculation based on the content of epigallocatechin gallate, a major component of green tea, and the species differences between experimental animals and humans, suggesting the preventive effectiveness in humans.

Animals↗

[The determination of phenols in water: gas chromatographic identification by means of the electron affinity (author's transl)].

The electron affinities for 98 phenolic compounds have been determined using an electron capture detector (ECD) and a flame ionisation detector (FID). The signals of the two detectors were registered simultanously on a two channel recorder by splitting the gas stream at the column outlet for the ECD and the FID (1:1). The peak areas were corrected for equal concentration and instrument parameters and the relation peak area (ECD)/peak area (FID) was used as a measure of electron affinity. The values thus measured are given in a table. Among the phenolics found in water there are several groups with high or very high electron affinity, e.g. dichlorophenols, trichlorophenols, tetra- and pentachlorophenol; the values of these compounds are about 10(2), 10(3), 10(4), and 3 times 10(4) times higher, respectively, than that of phenol itself and its alkyl derivatives. For the mono- and dinitrophenols the corresponding figures are between 10(2) (o-nitrophenol) and 5 times 10(3) (dinitrophenols). A comparatively high value was measured for salicylic aldehyde: about 2.5 times 10(2) compared with phenol. The application of these values in the identification of some peaks in the gas chromatogram of a river water extract is demonstrated.

Dinitrophenols↗

[Tetrabutyl titanate hydrolysis prepared TiO2 photocatalysis loaded with platinum technology].

Photocatalysts Pt/TiO2 coated on hollow glass beads were prepared by tetrabutyl titanate hydrolysis with Sodium silicate on hollow glass beads at various condition and loaded with platinum varying from 0.2% to 2.4% by weight. Sodium pentachlorophenolate (PCP-Na) solution were used to examined for their photoactivity and characterized by X-ray and BET. The results indicated that the optimization condition to prepare photocatalysts: Water to titanium alkoxides was 100, Sintering temperature was 650 degrees C, Diameter of hollow glass beads was 0.5 mm, TiO2: sodium silicate: hollow glass beads was 10:2.5:20, Platinum content of photocatalysts was about 1.4%-1.6%. When the experiments were carried out in such conditions, the initial concentration of PCP-Na was 100 mg/L, initial pH was 6.5, oxygen flux was 1.6 mL/s, illumination intensity was 30 kW.m-2, catalysts was 2 g/L, illumination time was 2 hours, respectively. Then the rates removals of PCP-Na could reach 92.0%.

Butanols↗

Photocatalytic degradation of PCP-Na with TiO2 photocatalysis loaded with platinum.

Titanium dioxide (TiO2) samples of different crystal forms were prepared by hydrolysis tetrabutyl titanate in various water to alkoxide ratios and sintering the hydrolysis product at different temperatures. The photocatalysts coated on hollow glass beads and loaded with platinum varying from 0.2% to 2.4% by weight. The photocatalytic degradation rate of sodium pentachlorophenolate (PCP-Na) depends on the preparing conditions such as: sintering temperatures, water to alkoxide ratios (R), platinum content and the size. The proper conditions of preparation photocatalysts are as follows: the ratio of TiO2: sodium silicate: hollow glass beads: platinum is 10:5:20:0.15 (w/w), R is 100, sintering temperature is 650 degrees C, and the size of hollow glass is 0.5-1 mm. Under these conditions, the ratio between acatase and rutile of the photocatalyst is 2:1, and the photocatalytic activity is high.

Catalysis↗

[Valve movement of the mussel Dreissena polymorpha as a monitoring system for bodies of water].

A new biological "early warning system" for continuous water control is presented that is based on the valve movements of the freshwater mussel Dreissena polymorpha. For two groups of up to 42 mussels, both the percentage of open mussels and the number of valve movements during a time interval are used to describe the activity behaviour of the zebra mussel. A main prerequisite of such a biomonitor should be the knowledge of the "normal" behaviour in correlation to changing environmental conditions. Preliminary results in Dreissena demonstrate the influence of the temperature, the daily cycle of light and the food concentration on both characteristics of the activity pattern. During toxicity tests, the mussels reacted significantly within 3-30 minutes after the addition of a toxicant. This was normally observed by both the decrease of the percentage of open mussels and the increase of the number of valve movements. Therefore--and against the background of the well-known "normal" behaviour--reliable limits for the detection of a harassing event can be defined. First experiments with Pentachlorophenol, Lindane, Atrazine and 2-Nitrophenol demonstrated to some extent a higher sensitivity compared to other "early warning systems".

Animals↗

[Use of bioreactors for continuous water monitoring].

A commercially available bacterial toxicity monitor ("Toxiguard", BTG Anlagentechnik, Bochum, Germany) was tested for continuous river monitoring. Operating with biofilms, this system shall detect toxic substances in the water. River water passes through two bioreactors forming a biofilm of characteristic river bacteria. The indicating parameter of the biomonitor is the respiration rate of this bacterial biofilter. The remaining oxygen content in the effluent from the biofilter is measured continuously by an oxygen electrode. This value is related to the dissolved oxygen (DO) of the river water measured in a by-pass. In presence of inhibitory substances the DO content in the biofilter increases because of the reduced respiration activity of the bacteria. The addition of nutrients may lead to an increase of biomass and of respiration activity. This results in an increasing oxygen difference between DO contents in the biofilter influent and effluent. Therefore, the degree of poisoning is better perceptible. Moreover each nutrient causes a distinct biofilm with a specific sensitivity against chemicals. This effect will be shown for Sodium-Pentachlorophenolate (Na-PCP).

Animals↗

PCP exposure for the Canadian general population: a multimedia analysis.

Pentachlorophenol (PCP) is ubiquitous in the Canadian environment, as a result of the large quantities used in the wood preservation and wood protection industries. In the past decade, agricultural and wood protection applications of PCP in Canada have been sharply curtailed. A multimedia approach was used to update estimates of PCP exposure of the members of the general population in Canada, based on currently available information. A detailed review of PCP concentrations reported in air, water, foods, household dust, and soil was performed. PCP intake estimates for infants, toddlers, school-age children, and adults in Canada were calculated. Estimates were made for people with average intakes of air, water, foods, household dust, and soil, as well as for recreational anglers and aboriginal subsistence fishermen, who were expected to have higher intakes. The current estimated intake by all of these populations is well below the Acceptable Daily Intake (ADI) of 6 micrograms/kg bw/day. The average members of the general population have an estimated intake via all routes of 0.05 micrograms/kg bw/day; most exposure is calculated to occur via food (dairy products, grains and cereals and meats) and indoor air. Recreational anglers are estimated to be exposed to only marginally more PCP per day (roughly 2%) than the general population. In contrast, aboriginal subsistence fisherman, because of their very high consumption of fish and fish products, experience the highest exposure to PCP through food; their estimated intake of PCP is almost twice that of the general population.

Adolescent↗