Toxicity of mercury,copper, nickel,lead, and cobalt to embryos and larvae of zebrafish,Brachydanio rerio

The toxicity of mercury (HgCl₂), copper (CuCl₂: 5 H₂O), nickel (NiSO₄: 6 H₂O), lead (Pb(CH₃COO)₂: 3 H₂O) and cobalt (CoCl₂: 6 H₂O) was studied under standardized conditions in embryos and larvae of the zebrafish,Brachydanio rerio. Exposures were started at the blastula stage (2–4 h after spawning) and the effects on hatching and survival were monitored daily for 16 days. Copper and nickel were more specific inhibitors of hatching than cobalt, lead, and mercury. Nominal no effect concentrations determined from the dose-response relationships (ZEPs, Zero Equivalent Points) for effect on hatching time were 0.05 g Cu/L, 10 g Hg/L, 20 g Pb/L, 40 g Ni/L and 3,840 g Co/L, and those for effect on survival time were 0.25 g Cu/L, 1.2 g Hg/L, 30 g Pb/L, 80 g Ni/L, and 60 g Co/L. The no effect concentrations for Ni, Hg and Pb are consistent with previously reported MATC values for sensitive species of fish. The no effect concentrations for copper are 1–2 orders of magnitude lower than previously reported values. The major reason for the latter discrepancy was considered to be the absence of organics that can complex copper ions in the reconstituted water that we used, which had a hardness of 100 mg/L (as CaCO₃) and a pH of 7.5–7.7. Unexposed controls were started with embryos from different parental zebrafishes and the parental-caused variability in early embryo mortality, median hatching time and median survival time were estimated.     

Human exposure to volatile halogenated hydrocarbons from the general environment

Summary The objective of this study was to assess individual human exposure to volatile halogenated hydrocarbons (VHH) under normal environmental conditions by means of biological monitoring, i.e. by the measurement of these compounds or their metabolites in body fluids, such as blood, serum, and urine. Blood samples of 39 normal subjects without known occupational exposure to these agents were examined for the occurrence of VHH. The following compounds were present in quantifiable concentrations in 60 to 95% of the blood samples examined: chloroform (median 0.2 g/l; range < 0.1–1.7 g/l), 1,1,1-trichloroethane (median 0.2 g/l; range < 0.1–3.4 g/l), tetrachloroethylene (median 0.4 g/l; range < 0.1–3.7 g/l). Trichloroethylene could be detected in 31% of all blood samples (median < 0.1 g/l; range < 0.1–1.3 g/l). In addition, the levels of trichloroacetic acid (TCA) were determined in serum and 24-h urine samples of 43 and 94, respectively, normal subjects. TCA was present in measurable concentrations in all serum and urine samples examined. The median of the TCA levels in serum was 21.4 g/l (range 4.8–221.2 g/l) and in urine 6.0 g/24 h (range 0.6–261.4 g/24 h). The results are discussed in relation to data from the literature on human exposure to VHH from the general environment, i.e. via air, food, and water. The upper normal limits calculated from the results of this investigation can be used to detect even minor excessive exposures to VHH.     

The effects of poly chlorinated biphenyls and methylmercury,singly and in combination on mink. II: Reproduction and kit development

Adult ranch-bred mink (Mustela vison) were fed diets containing either 0, 1.0 g/g polychlorinated biphenyls (PCB) (Aroclor^® 1254), 1.0 g/g methylmercury (MeHg), a combination of 1.0 g/g PCB plus 1.0 g/g MeHg, or 0.5 g/g PCB plus 0.5 g/g MeHg. Fertility of adult male mink, percentage of females whelped or number of kits born per female were not affected by the treatments. However, growth rate of kits nursed by mothers exposed to 1.0 g/g PCB was significantly reduced. There was a synergistic effect of PCB and MeHg which reduced kit survival in groups receiving both chemicals simultaneously. Kit survival to weaning in the control, 0.5 g/g PCB/MeHg, and 1.0 g/g PCB/MeHg groups was 72.0%, 62.7% and 35.8%, respectively. The results suggest that growth and survival of mink kits are adversely affected at dietary levels of PCB and MeHg currently present in some environments.     

In vitro susceptibility of mycelial and yeast forms of Penicillium marneffei to amphotericin B,fluconazole, 5-fluorocytosine and itraconazole

The mycelial (25°C) and yeast-like (37°C) forms of Penicillium marneffei clinical and type strains were investigated for their in vitro susceptibility to amphotericin B (AmB), 5-fluorocytosine (5-FC), fluconazole (FLU) and itraconazole (ITZ), using Bacto antibiotic medium 3, yeast-nitrogen, Sabouraud's dextrose (pH 5.7) and high resolution (pH 7.1) broth media (1ml/tube), respectively. Results indicated that the minimal inhibitory and minimal fungicidal concentrations (MICs and MFCs) for the mycelial cultures of P. marneffei to AmB were in the range 0.78–1.56 and 0.78–3.125 g/ml, respectively, as against 3.125–25 g (MICs) for the yeast form cultures. The MFCs to AmB for the yeast form were one dilution higher. The MICs to FLU were generally lower for the yeast form (6.25–25 g) than the mycelial form (25–50 g/ml), whereas MFCs for the mycelial cultures were > 100 g as compared to 6.25–100 g for their yeast form. The MICs for the mycelial form to 5-FC ranged from < 0.195–0.39 g. Higher MICs (6.25 g) were recorded for their yeast form. The MFCs to 5-FC for the yeast form were 25–100 g/ml. The MICs for the mycelial form to ITZ ranged from < 0.195 to 3.125 g/ml. Higher values (< 0.195–50 g) were recorded for their yeast-like form. The MFCs to ITZ for mycelial and yeast forms ranged from < 0.195–0.39 and 25–100 g/ml, respectively. Results indicate that P. marnefei's yeast form is more sensitive to FLU and ITZ (8 of 10 strains) while the mycelial form displayed greater susceptibility to AmB and 5-FC. The MICs for ITZ remained steady in SD medium, pH 5.7 to 7.1. However, some strains gave higher MIC values (0.39–1.56 g/ml) when tested in the HR.     

Monitoring of Antifouling Booster Biocides in Water and Sedimentfrom the Port of Osaka, Japan

Concentrations of booster antifouling compounds in the port of Osaka, Japan were assessed. Concentrations of Sea-Nine 211 (4,5-dichloro-2-n-octyl-3-isothiazolone), thiabendazole (2-(4-thiazolyl)-benzimidazole), IPBC (3-iodo-2-propynyl butylcarbamate), Diuron (3,4-dichlorophenyl-N, N-dimethylurea), Irgarol 1051 (2-methylthio-4-t-butylamino-6-cyclopropylamino-s-triazine), and M1 (2-methylthio-4-t-butylamino-6-amino-s-triazine) in port water samples were in the range of <0.003–0.004 g L^–1, <0.0008–0.020 g L^–1, <0.0007–1.54 g L^–1, <0.0008–0.267 g L^–1, and <0.0019–0.167 g L^–1, respectively. IPBC was not detected in the water samples, but the concentration of Diuron was higher than any previously reported. The concentrations of Sea-Nine 211, thiabendazole, Diuron, Irgarol 1051, and M1 in sediment samples were in the range of <0.04–2.4 g kg^–1 dry, <0.08–1.2 g kg^–1 dry, <0.64–1350 g kg^–1 dry, <0.08–8.2 g kg^–1 dry, and <0.18–2.9 g kg^–1 dry, respectively. IPBC was again not detected. The levels of Sea-Nine 211, Diuron, and Irgarol 1051 in water and sediment samples were high in a poorly flushed mooring area for small and medium-hull vessels. Levels of Diuron and Irgarol 1051 were highest in summer. The concentration of Sea-Nine 211 in water increased between August and October 2002. Except for M1, increases in the levels of booster biocides in sediment were observed during the study period. The sediment–water partition (Kd) was calculated by dividing the concentrations in sediment by the concentrations in water. The Kd values for Sea-Nine 211, thiabendazole, Diuron, Irgarol 1051, and M1 were 690, 180, 2700, 300, and 870. The Kd value for these alternative compounds was lower than for TBT.     

DDT,DDD, and DDE contamination of sediment in the Newark Bay estuary,New Jersey

Two hundred and forty-six surface and buried sediment samples from Newark Bay, New Jersey, and its major tributaries (Passaic River, Hackensack River, Newark Bay, Arthur Kill, Elizabeth River, and Kill Van Kull) were assayed for p,p-dichlorodiphenyltrichloroethane (p,p-DDT), p,p-dichlorodiphenyldichloroethane (p,p-DDD), and p,p-dichlorodiphenylchloroethylene (p,p-DDE) between February 1990 and March 1993. Chronological profiles in sediments from pre-1940 to the present were determined by radioisotope activities of ²¹⁰Pb and ¹³⁷Cs. The concentrations of these chemicals were compared to National Oceanic and Atmospheric Administration (NOAA) benchmark sediment values (Long and Morgan 1991). The objectives were to (a) determine the spatial and temporal distributions of DDT compounds in sediments, (b) identify possible sources, and (c) assess the potential for sediment toxicity within the estuary. Mean concentrations in surface sediments in individual waterways ranged from 5 to 473 g/kg for p,p-DDT, 18 to 429 g/kg for p,p-DDD, and 5 to 111 g/kg for p,p-DDE. A regional background mean concentration of approximately 100–300 g/kg p,p-DDT (sum of p,p-DDT, p,p-DDD, and p,p-DDE) was measured in surface sediments throughout the estuary, with the exception of the Arthur Kill, where mean concentrations exceeded 700 g/kg. The elevated concentrations found in recently deposited surface sediments in the Arthur Kill may be due to the presence of ongoing sources. The highest concentrations in buried sediments occurred in the lower Passaic River at depths corresponding to historical deposits from 1940 to 1970, the peak time period for production and usage of DDT in the United States. Comparisons to NOAA benchmark sediment toxicity values indicate that p,p-DDT, p,p-DDD, and p,p-DDE concentrations in surface sediments may pose a potential hazard to fish, shellfish, and other benthic and demersal organisms in some portions of the estuary, particularly in the upper and lower Arthur Kill.     

Toxicity of aldicarb and fonofos to the early-life-stage of the fathead minnow

Flow-through early-life-stage (ELS) toxicity tests were conducted with the pesticides aldicarb (Temik^®) and fonofos (Dyfonate^®) to determine their effect on the survival and growth of fathead minnows. Concentrations of 78g/L of aldicarb and 16g/L of fonofos did not affect survival and growth. However, 156g/L of aldicarb and 33g/L of fonofos were lethal to larval-juvenile exposed for 30 days post-hatch. The maximum acceptable toxicant concentration (MATC) of aldicarb and fonofos for the fathead minnow is estimated to be between 78–156g/L and 16–33g/L, respectively. The corresponding chronic values (geometric mean of MATC values) would be 110g/L and 23g/L. Acute toxicity tests gave 96-hr LC50 values of 1370g aldicarb/L and 1090g fonofos/L. The acute-chronic ratio (96-hr LC50/chronic value) is 12 for aldicarb and 47 for fonofos.     

Nitrous oxide in blood and urine of operating theatre personnel and the general population

Nitrous oxide (N₂O) was assayed in 676 urine samples and 101 blood samples provided after exposure by operating theatre personnel from nine hospitals. The blood and urine assays were repeated in 25 subjects 18 h after the end of exposure. For 80 subjects, environmental N₂O was also measured during intraoperative exposure. Mean urinary N₂O in the 676 subjects at the end of exposure was 40 g/l (range 1–3805 g/l); in 10 of the 676 subjects, urinary N₂O was in the range 279–3805 g/l (mean 1202 /l). The 98^th percentile was 120 g/l. Mean blood N₂O at the end of exposure, measured in 101 subjects, was 21 g/l (median 16 g/l, range 1–75 g/l). Blood and urine N₂O (1.5 g/l and 4.9 g/l, respectively) in 25 subjects, 18 h after exposure, was significantly higher than in occupationally non-exposed subjects (blood 0.91 g/l, urine 1 g/l). Environmental exposure was significantly related to blood and urinary N₂O (r = 0.59 andr = 0.64, respectively). Blood and urinary N₂O were significantly related to each other (r = 0.71), and were equivalent to about 25% of the environmental exposure level. The mean urinary N₂O of 1202 g/l in 10/676 subjects was not related to environmental exposure in the operating theatre. The highest urinary N₂O levels measured in these 10/676 subjects could be explained by an asymptomatic urinary infection.     

Chronic toxicity and bioaccumulation of 2,5,2′,5′- and 3,4,3′,4′-tetrachlorobiphenyl and Aroclor® 1242 in the amphipodHyalella azteca

The addition of 100 (g/L of Aroclor^® 1242 (A1242) or 2,5,2,5-tetrachlorobiphenyl (TeCB) during 10 week chronic toxicity tests withHyalella azteca resulted in complete mortality. There were no effects on survival, growth, or reproduction after addition of 30 g/L. Toxic effects were observed at tissue levels of between 30 and 180 g/g on a wet weight basis, and tissue levels appear to be a better indicator of toxicity than levels in water. No toxic effects were observed after additions of up to 2,700 g/L of the coplanar congener 3,4,3,4-TeCB.H. azteca has the ability to avoid accumulating in excess of 140 g/g 3,4,3,4-TeCB. The amount taken up was proportional to the amount added in water up to 100 g/L, but was constant at higher additions, possibly accounting for its relatively low toxicity. The low toxicity of the coplanar congener, as compared to the non-coplanar 2,5,2,5-TeCB, is in direct contrast to the high toxicity of coplanar PCB congeners to mammals and may be associated with slower rates of aromatic hydrocarbon metabolism in amphipods. Polychlorinated biphenyl levels measured in amphipods from Lake Ontario are approximately 100-fold below levels associated with toxicity inH. azteca, but are above levels which, through biomagnification up the food chain, lead to salmonid residues in excess of 2 g/g, a tolerance limit for human consumption.     

Biological and environmental monitoring of occupational exposure of pharmaceutical plant workers to methotrexate

Summary The exposure of 11 pharmaceutical plant workers to methotrexate (MTX) was studied. Personal air samples were taken during the different manufacturing processes: drug compounding, vial filling, and tablet preparation. The uptake of MTX was established by the determination of MTX in urine. MTX was analyzed using the fluorescence polarization immunoassay (FPIA), a method that is frequently used for monitoring serum levels in patients treated with MTX. The FPIA method was modified in such a way that MTX could be measured quickly and efficiently in air and urine samples. MTX was detected in air samples of all workers except for those involved in the vial filling process (range: 0.8–182 g/m³; median: 10 g/m³). The highest concentrations were observed for workers weighing MTX (118 and 182 g/m³). MTX was detected in urine samples of all workers. The mean cumulative MTX excretion over 72–96 h was 13.4 g MTX-equivalents (range: 6.1–24 g MTX-equiva g MTX-equivalents (range: 6.1–24 g MTX-equivalents). lents). A significantly lower background level of 10.2 g A significantly lower background level of 10.2 g MTX-equivalents was measured in urine of 30 control persons (range: 4.9–21 g MTX-equivalents).     

Lead exposure in indoor firing ranges

Summary Higher air lead levels (time-weighted average 660, range 112–2238 g/m³) were measured in firing ranges where powder charges were employed than in ranges where air guns were used (4.6, range 1.8–7.2 g/m³); levels in the latter were in turn higher than those in ranges used for archery (0.11, range 0.10–0.13 g/m³) Twenty-two marksmen who used powder charges had significantly increased blood lead levels during the indoor shooting season (before: median 106, range 32–176 g/l; after: 138; range 69–288 g/l; P = 0.0001), while 21 subjects who mainly used air guns displayed no significant increase (before: median 91, range 47–179 g/l; after: 84; range 20–222 g/l). Thirteen archers had significantly lower levels than the pistol shooters before the season (P = 0.006), and showed a significant decrease during the season (before: median 61, range 27–92 g/l; after: 56; range 31–87 g/l; P = 0.04). At the end of the indoor season, there was a significant association between weekly pistol shooting time and blood lead levels.     

Pesticide and PCB residues in the upper Snake River ecosystem,Southeastern Idaho,following the collapse of the Teton Dam 1976

The Teton Dam in Southeastern Idaho collapsed on June 5, 1976. The resulting flood damaged a large area and caused the release of toxicants into the Snake River. A pesticide recovery team in a helicopter worked the flooded area for three weeks and collected 1,104 containers, about 35% of which contained toxicants. It was estimated that less than 60% of the lost pesticide containers were recovered.This paper addresses the results of a one-time sampling effort designed to determine the magnitude of the chemical contamination. Over 300 samples of fish, plankton, waterfowl, sediments, water, stream drift, aquatic plants, and soil were taken. Pesticide residues were measured asg/kg (ppb) wet weight, whole animal basis. Rainbow trout had as much as 1432g/kg total DDT plus analogs, 66g/kg dieldrin, and 1010g/kg PCBs. Utah suckers had up to 1420g/kg total DDT plus analogs, 32g/kg dieldrin, and 1800g/kg PCB. Rocky Mountain whitefish had as much as 2650g/kg total DDT and analogs, 30g/kg dieldrin and 1400g/kg PCBs. These PCB and DDT levels were high, approaching the 2,000g/kg FDA proposed tolerance, but were below the 5,000g/kg present tolerance. Dieldrin levels were low and organophosphates were undetectable.An undeveloped area (the Fort Hall Bottoms) showed higher levels of contaminants than did an industrialized area (the lower Portneuf River). This apparent discrepancy remains unexplained.Very little pre-flood data on a whole fish basis were available for comparison (Johnsonet al 1977). However, it does not appear that any human health hazard due to pesticide levels exists in this portion of the Snake River.     

Bioaccumulation and toxicity of selenium in Chironomus decorus larvae fed a diet of seleniferous Selenastrum capricornutum

The bioaccumulation and toxicity of selenium in a simple aquatic food chain was investigated by feeding a diet of seleniferous algae (Selenastrum capricornutum) to fourth instar midge (Chironomus decorus) larvae. Treatment diets consisted of S. capricornutum cultured in three concentrations of selenite (0, 10, and 40 g Se/L) and four concentrations of selenate (0, 4, 10, and 40 g Se/L). The seleniferous algae was freeze-dried and utilized as a diet for the midge larvae. The data show that, under laboratory conditions, a 96 h dietary exposure of 2.11 g Se/g dry weight significantly reduced larval growth at tissue concentrations 2.55 g Se/g dry weight. The results demonstrate that some invertebrates are very sensitive to dietary selenium exposure. When compared to similar studies with Daphnia magna, the data suggest that invertebrate primary consumers differ in the metabolism of dietary selenium.     

Determination of the urinary metabolites of styrene: estimation of the method evaluation function and evaluation of reference values in Danish subjects

Summary A European study on styrene exposure was initiated in 1989 to evaluate the health effects of environmental and occupational exposure. A part of this study included the development of an analytical method for use in a biological monitoring program. The urinary metabolites of styrene, mandelic acid (MA) and phenyl-glyoxylic acid (PGA) were quantitated by a direct and convenient high-performance liquid chromatography method. Urine samples were diluted with eluent and analysed by HPLC with a C₈ reversed-phase column and a buffer to acetonitrile (9:1) eluent with a counterion added. The detector used was a variable UV dectector and the wavelength was = 210 nm. The method was statistically evaluated by a method evaluation demonstrating no systematic error. The uncertainty was 23.8 mol/l and 11.5 mol/l for MA and PGA, respectively. The limit of detection (LOD) of MA is 71.4 mol/l and the LOD of PGA is 34.5 mol/l, sufficiently low for the measurement of styrene exposure at a low exposure level. The present study indicates that reference values for MA and PGA are low. The fraction of reference values below LOD was 0.80 for MA and 0.66 for PGA; consequently, the reference values were described by a non-parametric one-sided tolerance interval. The 95% one-sided upper tolerance limits calculated for MA and PGA were 31.0 mol/mmol creatinine and 20.1 mol/mmol creatinine, respectively, with the coverage 0.95 ±0.045 for both metabolites. The method has been used for biological monitoring in several studies of environmentally and occupationally exposed subjects in concentrations up to 200 mol/mmol creatinine for MA and 150 mol/mmol creatinine for PGA.     

Biological effects of epidermal growth factor and 2,3,7,8-tetrachlorodibenzo-p-dioxin on developmental parameters of neonatal Mink

Newborn mink (Mustela vison) kits were administered 0.1 g 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD)/kg body weight, 1g TCDD/kg body weight, 10g epidermal growth factor (EGF)/ kg body weight, or 50 (g EGF/kg body weight by intraperitoneal (i.p.) injection (10 ml/kg body weight) for 12 consecutive days to compare the effects of TCDD and EGF on body weight gains, time of eyelid opening, tooth eruption, and pelage development. A 19 acetone-corn oil mixture and 0.85 NaCl served as vehicle controls for the TCDD and EGF groups, respectively. Mortality exceeded 50% at the higher doses of both TCDD and EGF, while at the lower doses, TCDD and EGF resulted in significant reduction of body weight gains. Additionally, EGF caused a significant decrease in the time of eyelid opening and retarded growth and development of the fur of the treated kits. TCDD had no discernible effects on the time of eyelid opening or hair growth. The time of tooth eruption was not significantly affected by either compound.Published with the approval of the Michigan Agricultural Experiment Station as Journal Article No. 12216.     

Cadmium and mercury in sediment and burrowing mayfly nymphs (Hexagenia) in the upper Mississippi River,USA

Longitudinal patterns in the cadmium and mercury content of burrowing mayflies (Hexagenia) and surrounding sediments were examined along a 572-km reach of the upper Mississippi River. Surficial sediments and Hexagenia nymphs were sampled in 1989 at 12 sites extending from Pool 2 through Pool 16 and analyzed for total recoverable cadmium and total mercury. In sediment and nymphs, concentrations of both metals were highest in Pools 2, 3, and 4, which are just downstream from the Twin Cities (Minneapolis-St. Paul, Minnesota) metropolitan area, the primary anthropogenic source of metals to the studied reach of river. Concentrations of the two metals in sediments indicated a significant anthropogenic contribution, which was most pronounced for cadmium. The cadmium concentrations in surficial sediment varied less than 3-fold (range, 1.19–3.23 g/g dry weight) among the 12 sites, whereas concentrations in Hexagenia varied almost 20-fold (range, 0.13–2.35 g/g dry weight). Nymphs from Pools 2–4 had much greater concentrations of cadmium than nymphs from sites further downstream, even though the mean concentration of cadmium in sediment from Pools 2–4 (3.0 g/g) was just twice that (1.6 g/g) for the nine sites downstream. Mercury in sediments from the 12 sites ranged from 0.038 to 0.165 g/g dry weight, averaging 0.14 g/g in Pools 2–4 and 0.056 g/g in the nine sites downstream. In nymphs, mercury concentrations ranged from 0.041 to 0.134 g/g dry weight. The bioavailability of sediment-associated cadmium seemed greater in Pools 2, 3, and 4 than in the sites further downstream, based on the relative cadmium concentrations in Hexagenia nymphs and sediment. Moreover, it is concluded that the trapping of sediment and associated metals in Lake Pepin (a natural riverine lake in Pool 4) significantly reduces the exposure of the ecosystem further downstream to metals from the Twin Cities and other upstream anthropogenic sources.Journal Paper No. J15705 of the Iowa Agriculture and Home Economics Experiment Station, Ames, IA. Project No. 2627     

Sublethal Effects of Trace Metals (Cd,Cr, Cu,Hg) on Embryogenesis and Larval Settlement of the Ascidian <Emphasis Type="Italic">Ciona intestinalis</Emphasis>

Toxicity of Cadmium (Cd), Chromium (Cr), Copper (Cu), and Mercury (Hg) on the early developmental stages of Ciona intestinalis was investigated. Developmental defects of larvae after exposure of gametes throughout their development to the larval stage were assessed. Gamete exposure to increasing metal concentrations resulted in a significant decrease of the percentage of normally hatched larvae, showing median effective concentrations (EC₅₀) of 721 g/L (6.42 M) for Cd, 12772 g/L (226 M) for Cr, 36.6 g/L (0.576 M) for Cu, and 44.7 g/L (0.223 M) for Hg. Larval attachment was significantly affected when gametes were exposed to the metals throughout development. The EC₅₀ reducing larval attachment by 50% were 752 g/L (6.7 M) for Cd, 15026 g/L (289 M) for Cr, 67.8 g/L (1.607 M) for Cu, and 78.1 g/L (0.389 M) for Hg. Therefore, on a molar basis Hg is three times more toxic than Cu, 20–30 times more than Cd, and 700–1000 times more toxic than Cr, for both responses.     

Toxicity of microencapsulated permethrin to selected nontarget aquatic invertebrates

Microencapsulated permethrin (penncapthrin) was evaluated under laboratory conditions for its toxicity toward several nontarget aquatic invertebrates. Average LC50 estimates for selected lotic invertebrates, based on a one hour dosing regime, were: 2.71 mg/L forSimulium vittatum, 4.59 mg/L forHydropsyche spp., and 13.41 mg/L forIsonychia bicolor. In acute static tests withDaphnia magna, there was no significant difference (p0.05) between the toxicity of penncapthrin at 96 h (LC50 range: 6.80–22.5 g/L) and the EC formulation at 72 h (LC50 range: 0.6–21 g/L). Comparatively, the toxicity of microencapsulated methyl parathion (penncap-m) was not significantly different from that of penncapthrin towardD. magna, the former having LC50 estimates ranging form 0.3–12.25 g/L. LC50 estimates associated withDaphnia pulex ranged from 19 to 131 g/L. The toxicity of penncapthrin and penncap-m towardD. pulex was difficult to determine because of frequent control mortality due to food deprivation resulting from the need to run tests for longer than 48 h. In successful tests, LC50 estimates ranged from 19 to 28 g/L for penncapthrin and 0.08 to 25 g/L for penncap-m after 72 h exposure. In long term toxicity tests, 95% of D. magna at 1 g/L, 44% at 10 g/L, and 20% at 15 g/L survived after 39 days exposure. Less than 15% ofD. pulex survived over the same concentration range following 32 days exposure. Despite some drawbacks, long-term toxicity tests were more appropriate than short-term tests for evaluating microencapsulated sticides because of reduced variability in LC50 estimates and lower control mortality.     

Long-term effects of dinoseb and paraquat,both individually and combined,on embryonic development and hatching success ofFasciola hepatica miracidia

Toxic effects of the herbicides dinoseb and paraquat, both individually and combined, on embryonic development and hatching ofFasciola hepatica miracidia were assessed by exposing the eggs to varying concentrations (0–20 g/ml) of each of the herbicides. The results showed that dinoseb has an LC₅₀ value of 4.3 g/ml, paraquat has an LC₅₀ of 4.9 g/ml and the mixture of both dinoseb and paraquat has an LC₅₀ of 7.1 g/ml. Based on the LC₅₀ values, dinoseb is slightly more toxic than paraquat on the tested organisms. The results also showed that the mixture of dinoseb and paraquat is significantly less toxic than the individual pesticides.Eggs ofF. hepatica cultured in either dinoseb or paraquat both individually and combined showed a delay of embryonic development and hatching of the miracidia. Eggs cultured in 0–2 g/ml of dinoseb, paraquat and their mixture, fully embryonated and hatched within 14–16 days, while eggs cultured in 4–6 g/ml of the same herbicides showed a delay of four days for embryonic development and hatching of their miracidia.     

Biological effects of Kepone and mirex in freshwater invertebrates

Acute and chronic toxicity studies of Kepone^® (chlordecone) and mirex were conducted with daphnids (Daphnia magna), amphipods (Gammarus pseudolimnaeus), and larvae of a midge (Chironomus plumosus). Acute toxicities of Kepone ranged from a 48-hr EC50 of 350g/L for midges to a 96-hr LC50 of 180g/L for amphipods, whereas the acute toxicities of mirex to all three taxa exceeded 1000g/L. Maximum acceptable toxicant concentrations (MATC's) for Kepone and mirex were estimated by measuring reproduction of daphnids, growth of amphipods, emergence of midges, and survival of all organisms. MATC for Kepone was estimated to be between 9 and 18g/L for daphnids, between 1 and 2g/L for amphipods, and between 8.4 and 18g/L for midges; MATC for mirex exceeded 34g/L for daphnids and midges, but less than 2.4g/L for amphipods. The concentration of Kepone and mirex accumulated by daphnids was 760 and 8025 times, respectively, the concentration in water. Estimated times for elimination of 50% of the residues by daphnids were 141 hr for Kepone and 12 hr for mirex.