In vitro and in vivo inhibition of Ca2+-Mg2+-ATPase activity by cadmium in post larvae of Penaeus monodon

Ca²⁺-Mg²⁺-ATPase is a membrane-bound enzyme and is responsible for regulating cytosolic free calcium. In vitro and in vivo effects of cadmium were studied on Ca²⁺-Mg²⁺-ATPase activity in plasma membrane/mitochondrial fraction of Penaeus monodon post larvae. In vitro studies revealed a concentration-dependent decrease in enzyme activity with an IC₅₀ value of 11.02?µM. In vivo experiments were conducted by exposing the post larvae to 1/10th (0.12?ppm) and 1/5th (0.24?ppm) of LC₅₀ values of cadmium for 30 days. Both ATPase activity and metal accumulation were estimated in post larvae exposed to 0.12 and 0.24?ppm of cadmium at different intervals of 24?h, 48?h, 96?h, 10 days and 30 days. ATPase activity showed a gradual decrease in post larvae on exposure to both the sub-lethal concentrations with respect to their controls and the decrease was significant (p?相似文献   

PCB disposition and different biological effects in rats following direct soil exposure vs. PCBs off-gassed from the soil

A comparison of PCB congener profiles and limited biological effects was made between direct exposure to PCB-contaminated soil and vapor phase PCBs from that soil to determine congener patterns useful for identifying exposure sources in humans and wildlife. Weanling female Sprague–Dawley rats were exposed to either control or PCB-contaminated soil (from a landfill in Southern Illinois) for 1 and 2 weeks. The exposures were via direct contact with the soil or via airborne exposure with the rats isolated from the soil by a wire screen. Total PCB of 25% contaminated soil used in the study was 13?500?ppm. No PCBs were detectable in control rats. In direct-exposed rats, total PCB residues in fat pad, ear skin, serum, liver, and inguinal lymph nodes after the 1-week exposure were 6256, 185, 3.2, 149, and 41?ppm, respectively, but decreased to 465, 72, 1.7, 106, and 32.4?ppm after the 2-week exposure. In airborne-exposed rats, total PCB residues were 7.8, 1.6, 0.03, 0.2, and 0.6 in the same manner and slightly increased in fat pad and ear skin to 11.6 and 2.14, respectively. Decreases in both the concentrations and percentages of “episodic” PCBs (those congeners rapidly metabolized) in the fat pad were apparent following the 2-week exposure compared to the 1-week exposure by both routes. Both EROD and BROD activities were significantly increased in the direct-exposed rats, whereas only BROD activity increased in airborne-exposed rats. Serum T ₄ levels were depleted in the direct-exposed rats regardless of time of exposure but were increased insignificantly after 1-week and significantly after 2 weeks in the airborne-exposed rats. No significant changes in serum insulin levels were apparent in any of the treated groups. The results suggested that exposure of animals to PCBs via different routes could result in different PCB profiles, which could cause different biological effects.     

Acute toxicity of ammonia to a freshwater teleost,Labeo bata larvae

Ammonia toxicity tests were performed with Labeo bata (bata) larvae of three different size groups. One hundred percent survival of larvae (500.0?±?4.0?mg) was recorded when exposed to ammonia concentrations of 1.0–13.56?mg?L^?1 at 96?h of exposure. Bata larvae exposed to ammonia concentrations of 15.8–25?mg?L^?1 showed 10–74% mortalities. The 96?h LC₅₀ value for 200 (±5), 250 (±2) and 500 (±4) mg bata larvae were 11.5, 16.8 and 22.5?mg?L^?1 un-ionised ammonia concentrations, respectively. When fish were exposed to different doses of ammonia, behavioural changes immediately occurred even at the lowest dose. At first, the fish became hyperexcitable, the skin darkened and they showed an increased ventilation frequency, fish behaviour became normal, 24?h after exposure. A 96?h LC₅₀ value of un-ionised ammonia showed direct relationship with the increasing size of bata larvae.     

Acute toxicity bioassay using Paramecium caudatum,a key member to study the effects of monocrotophos on swimming behaviour,morphology and reproduction

The toxic effects of an organophosphorous insecticide, monochrotophos (MCP) were investigated on Paramecium caudatum in static acute toxicity tests (10?min and 2?h). The lethal concentrations (50%) were determined by probit method, for technical monocrotophos as 60 and 40.6?mg?L^?1, respectively. We have combined conventional light microscopy and a computerized video tracking system to determine behavioural and morphological changes in paramecium on exposure to MCP. Paramecia exposed to highest concentrations (90–100?mg?L^?1) used for 10?min exposure, exhibited initial increase with subsequent decrease in mobility with enormous blebbing, leading to lysis of cells. In the second set of experiments, the cells exposed to lethal concentration (40.6?mg?L^?1) for 2?h were under stress, and reduced their locomotor behaviour, i.e. distance travelled per unit time (mm in 6?min) and swimming speed (mm?s^?1) with increased time of exposure. In the third set of experiments, the number of generations and generation time in 24?h was evaluated with respect to the different sub lethal concentrations (5, 10, 15 and 20?mg?L^?1) of toxicant. The number of generations decreased and generation time extended significantly in a concentration dependent manner. The results indicate that the Paramecium toxicity assay could be used as a complimentary system to rapidly elucidate the cytotoxic potential of insecticides.     

羰基镍急性中毒对大鼠骨髓细胞的DNA损伤

通过动物实验观察不同剂量羰基镍对大鼠骨髓细胞DNA损伤程度。采用SD大鼠,以135 mg·m~(-3)和250 mg·m~(-3)羰基镍为染毒组,250 mg·m~(-3)氯气为阳性对照组,静态方式染毒30 min。未染毒组为正常对照组,大鼠染毒后1、2、3和7 d分别采集样本。采用单细胞凝胶电泳检测每组大鼠骨髓细胞DNA的损伤程度。彗星尾长和Olive尾矩2个指标的分析结果表明,大鼠骨髓细胞DNA损伤程度随着羰基镍染毒剂量的增加而增加,在4个时间点各剂量组间均有显著差异(P0.05)且随时间的变化有一定的规律,损伤程度在3 d时达到最大,而后缓慢下降。羰基镍急性中毒对大鼠骨髓细胞DNA有一定的损伤,且存在剂量-效应关系,各剂量组损伤程度有一定的时间效应规律。     

Toxic effects of phosphoramidate on Paramecium sp. with special emphasis on respiratory metabolism,growth, and generation time

The toxicological impacts of the increasing number of synthetic compounds present in the aquatic environment are assessed predominantly in laboratory studies where test organisms are exposed to a range of concentrations of single compounds. Protozoan cells are often used as bioindicators for the presence of xenobiotic compounds. In this article, we describe the inhibitory effect of a synthetic phosphoramidate derivative at different concentrations (40, 60, and 80?µmol?L^?1) on Paramecium sp., affecting its growth (proliferation) in concentration-dependent manner, as well as the generation time and response percentage. The LC₅₀ value determined for these protozoa was estimated at 60?µmol?L^?1 on 24?h of exposure. The respiratory metabolism of protozoan is perturbed at three concentrations, noting that the oxygen consumption was significantly increased at high concentrations after 18?h of exposure. In addition, the data can be used as reference values in further testing with other pesticides.     

Effects of deltamethrin on serum calcium and corpuscles of Stannius of freshwater catfish,Heteropneustes fossilis

Adult male deer mice were exposed every other day for a period of 11 days to either 7,12-dimethylbenzanthracene (DMBA; CAS# 57-97-6) or benzo[b]fluoranthene (BbF; CAS# 205-99-2) (0, 0.3, 1, 3, 10, or 30?mg?kg^?1). Immune endpoints assessed were lymphocyte proliferation, macrophage pinocytosis, and the antibody plaque-forming cell (PFC) response. Cytochrome P450 (CYP450) activity was assessed using ethoxyresorufin-O-deethylase (EROD) and pentoxyresorufin-O-deethylase (PROD). Macrophage pinocytosis was not altered by either compound. Both T- and B-cell proliferations were significantly increased by DMBA at 0.3 or 1?mg?kg^?1 and by BbF at 10 or 30?mg?kg^?1, but decreased by DMBA at 30?mg?kg^?1. Sheep red blood cell (SRBC)-specific-IgM production, as measured by the PFC response, was the most striking adverse immune effect observed and was significantly suppressed compared to control at all treatment concentrations for both compounds. EROD activity was markedly induced by DMBA at 30?mg?kg^?1, while BbF produced induction at 1, 10, or 30?mg?kg^?1. No marked effect on PROD activity was noted following DMBA treatment, but BbF-induced PROD activity at 1, 10, or 30?mg?kg^?1. Unexpectedly, four of six mice in the 30?mg DMBA?kg^?1 group did not survive to the end of the experiment, and one animal died in both the 3 and 10?mg?kg^?1 treatments. The calculated LD₅₀ was 20.8?mg DMBA?kg^?1. The PFC response in deer mice was a more sensitive endpoint than CYP450 activity, suggesting that utilization of CYP450 endpoints in risk assessment without assessment of immune function, specifically antibody production, might possibly underestimate the risk to wild rodents environmentally exposed to polycyclic aromatic hydrocarbons.     

Acute toxicity of benzophenone-type UV filters and paraben preservatives to freshwater planarian,Dugesia japonica

Fourteen benzophenone-type UV filters and four paraben preservatives were selected to examine their acute toxicities on Dugesia japonica. The 48-h LC₅₀ values for planarians exposed to benzophenone-type UV filters can be ranked as oxybenzone?>?mexenone?>?5-chloro-2-hydroxybenzophenone?> 2,4-dihydroxybenzophenone?>?2-hydroxybenzophenone?>?dioxybenzone?>?benzophenone?>?2,2′,4,4′-tetrahydroxybenzophenone?>?4-hydroxybenzophenone?> 3-hydroxybenzophenone?>?4,4′-dihydroxybenzophenone?>?2,2′-dihydroxy-4,4′-dimethoxybenzophenone?>?2,3,4-trihydroxybenzophenone?>?sulisobenzone with a range from 0.9 to 145?mg?L^?1 with a similar sequence for the 96?h LC₅₀ values, ranging from 0.5 to 77?mg?L^?1. The 48 and 96?LC₅₀ values for planarians exposed to paraben preservatives can be ranked as butylparaben?>?propylparaben?>?ethylparaben?>?methylparaben. Among all the tested chemicals, oxybenzone was the most toxic and sulisobenzone the least toxic chemical to planarian at each exposure period. Most benzophenone-type UV filters are toxic to aquatic animals with 48?h LC₅₀ values less than 10 mg?L^?1, except for 2,2′-dihydroxy-4,4′-dimethoxybenzophenone, 2,3,4-trihydroxybenzophenone, and sulisobenzone. Because of their common occurrence in aquatic environment, more studies on aquatic toxicities of benzophenone-type UV filters and paraben preservativs are needed to provide important information to adequately assess their ecological risk.     

内质网应激在PFOS致大鼠肝损伤中的作用

通过全氟辛烷磺酸(PFOS)28 d大鼠经口染毒评价PFOS肝损伤效应,探讨内质网应激在PFOS毒效应中的作用。Wistar大鼠随机分组,分别以0 mg·kg~(-1)、5 mg·kg~(-1)和10 mg·kg~(-1)PFOS灌胃染毒28 d。HE染色观察大鼠肝脏形态改变。ELISA法测定各组丙氨酸转氨酶(ALT)、天门冬氨酸转氨酶(AST)、碱性磷酸酶(ALP)和淀粉酶(AMY)含量变化。紫外分光光度法测定肝组织匀浆中丙二醛(MDA)、超氧化物歧化酶(SOD)、谷胱甘肽过氧化物酶(GSH-Px)活性变化。RT-PCR检测肝脏内质网应激标志蛋白表达水平。结果表明,PFOS造成大鼠体重降低、肝重增高(P0.05),组织切片显示肝细胞出现脂质沉积。PFOS不同剂量组大鼠ALT随暴露浓度增加,分别为(50.96±10.02)U·L~(-1)、(71.73±11.55)U·L~(-1),显著高于对照组(P0.05),AST、ALP含量与对照组相比显著上升(P0.05),高剂量组AMY水平为(833.46±63.05)U·L~(-1),与对照组相比显著降低(P0.05)。GSH-Px和SOD水平随PFOS浓度增加出现了显著降低(P0.05),而MDA水平显著升高(P0.05)。内质网应激标志蛋白表达均较对照组显著上升(P0.05)。以上结果说明PFOS可导致大鼠肝细胞损伤,其机制可能与内质网应激调控有关。     

The microcystins-induced DNA damage in the liver and the heart of zebrafish,Danio rerio

Microcystins (MCYST) are the freshwater cyanobacterial toxins, known to induce hepatocellular carcinoma, necrosis, intrahepatic bleeding, as well as human and livestock mortality. Within hepatocytes, MCYST selectively bind to protein phosphatases 1 and 2A, resulting in severe liver damage. The toxicology of MCYST in mice and rats has been well studied, but little is known regarding genotoxicity in aquatic animals. In this study, the zebrafish, Danio rerio was exposed to crude extract of Microcystis aeruginosa bloom. Liver and heart were examined for MCYST-induced toxicity. Light microscopy at 36?h revealed severe, widespread apoptotic necrosis of the majority of hepatocytes, and cytoskeletal deformation in myocardiocytes. Hepatocytes were dissociated with cell shrinkage and margination of nuclear chromatin. Laddering of genomic DNA from the liver and heart of the exposed fish in an increment of 180–200?bp was consistent with apoptosis. Fluorimetric analysis of DNA unwinding was carried out to determine the DNA strand breakage. After 36?h exposure, the % double-stranded DNA was significantly reduced in hepatocytes and myocardiocytes. In conclusion, the results obtained in this study indicate that, the extract of M. aeruginosa bloom is genotoxic to fish. The DNA damage observed in this study may be attributed to the activation of DNA endonucleases. This model of DNA damage may contribute for identifying novel molecular mechanisms of interest for therapeutic application.     

Automatic sorting of zooplankton by isopycnic sedimentation in gradients of silica: Performance of a “Rho Spectrometer”

The embryonic and larval stages of the quahog clam Mercenaria sp. were exposed to the water-soluble fractions (WSFs) of 6 oils and the effects on survival and growth rate of the various stages were noted. Kuwait crude oil was the least toxic on initial exposure to both stages, having LC₅₀ values in excess of 10 ppm after continuous exposure to the WSF for up to 6 days. However, at 10 days, Kuwait was slightly more toxic than southern Louisiana crude oil, with both oils having LC₅₀ values near 2 ppm. Florida Jay crude oil was much more toxic, with an LC₅₀ of less than 1 ppm at 48 h and less than 0.2 ppm at 10 days. Two refined oils, No. 2 fuel oil and Bunker C, had LC₅₀ values of 1 to 2 ppm after 48 h, while used crankcase motor oil, the most toxic oil tested, had LC₅₀ values of 0.10 ppm or less at all exposure times. Larvae surviving exposure to water-soluble fractions of the various oils often grew at slower rates than the controls.     

Gender-based comparative toxicity of di-ethyl phthalate in Wistar rats

In recent years, the exposure of humans to phthalate esters through environmental contamination has increased. One among them is di-ethyl phthalate (DEP), which is used as a plastisizer for cellulose ester plastic films and sheets, solid rocket propellants, molded and extruded articles, as a component in insecticide sprays and various other substances, as well as in industrial applications. Release into the environment occurs primarily as a result of production and manufacturing of DEP and during the use and disposal of products containing DEP. Therefore, a study was undertaken to evaluate gender-specific toxicity of DEP in Wistar rats. Rats of both sexes, weighing 125–130?g, were administered 50?ppm (w/v) DEP in water ad libitum for a period of 180 days and were given normal diet. Control animals received normal diet and water ad libitum. During the treatment, rats were weighed every week and water consumption per day was measured. After the completion of treatment, liver weight?:?body weight^?1 ratio, liver weight, body weight^?1, liver and serum enzymes, and other biochemical parameters of liver and serum were assessed. It was observed that there was no significant change in body weight^?1, liver weight, liver weight?: body weight^?1 ratio, and water consumption in both sexes. There were significant increases in liver acid phosphatase (ACP) activity and kidney glutathione levels, and nonsignificant changes in liver alkaline phosphatase (ALP), aspartate aminotransferase (AST), alanine aminotransferase (ALT), succinate dehydrogenase (SDH), and lactate dehydrogenase (LDH) activities in DEP-treated male rats, whereas in DEP-treated female rats the liver showed significant decrease in ALP and SDH and nonsignificant changes in AST, ALT, and LDH activities. Serum ACP and LDH levels in DEP-treated male rats were significantly decreased, and in the case of DEP-treated female rats, only serum LDH levels were significantly decreased. There was no significant change in serum ALP, AST, and SDH levels in DEP-treated male and female rats as compared to control rats. Histology of the livers of both male and female rats showed loss of hepatic architecture, degenerative changes in hepatocytes, and vacuolation in hepatocytes in both the centrilobular and periportal areas. It can be concluded from this study that prolonged exposure to DEP at 50?ppm levels can be harmful to animals and humans. This is evident from the present study as certain significant changes in enzyme activities in the liver, serum, and histological alterations in liver were observed.     

Acclimation and tolerance of Artemia salina to copper salts

The brine shrimp Artemia salina L. was acclimated in sea water with cupric chloride, acetate, carbonate, and sulphate, each at concentrations of 0.1, 0.05 and 0.025 ppm Cu⁺⁺, together with sea water controls. Growth inhibition was observed in all four compounds, generally in direct relationship to the concentration. It was least in sulphate, and increased progressively in chloride, acetate and carbonate in that order. No inhibition however was observed in carbonate at 0.025 ppm Cu⁺⁺. In toxicity tests, 2-week old larvae from each solution were exposed to concentrations of 10, 7.5, 5, 2.5 and 1 ppm Cu⁺⁺ of the same compounds, together with unacclimated larvae of the same age. Similar tests were held with 6-week old adults acclimated (a) in 0.1 ppm Cu⁺⁺ (chloride, acetate and sulphate) using the same concentrations and (b) in 0.5 ppm Cu⁺⁺ (carbonate), using 150, 125, 100, 75, and 50 ppm Cu⁺⁺. Toxicity to unacclimated larvae and adults differed with the compounds, carbonate being the least toxic, followed by sulphate, chloride and acetate in increasing order. Larvae acclimated in chloride (0.025 ppm Cu⁺⁺) and sulphate (0.1 and 0.5 ppm Cu⁺⁺) showed an increased tolerance to 1 and 2.5 ppm Cu⁺⁺ compared to untreated controls. Tolerance was not enhanced from 5 ppm Cu⁺⁺ upwards. In both compounds, adults acclimated in 0.1 ppm Cu⁺⁺ showed an increased tolerance to concentrations between 1 and 7.5 ppm Cu⁺⁺ compared to controls. Larval mortality in carbonate was below 50% in all test solutions. Adults acclimated at 0.5 ppm Cu⁺⁺ showed an increased tolerance to 50 ppm Cu⁺⁺ compared to controls. Considerable precipitation occurred with the high levels of this compound, thus effecting the final concentrations. No acclimation effect was observed in acetate for either larvae or adults. It is suggested that in A. salina, copper toxicity depends on the particular form of the metal, and that this difference is also evident in growth inhibition and in the potential acquisition of increased tolerance through exposure to low concentrations.     

Early murine immune responses from endotracheal exposures to biotechnology-related Bacillus strains

An immunology-based in vivo screening regime was used to assess the potential pathogenicity of biotechnology-related microbes. Strains of Bacillus cereus (Bc), Bacillus subtilis (Bs), Bacillus thuringiensis (Bt), and Bt commercial products (CPs) were tested. Balb/c mice were endotracheally instilled with purified spores, diluted CP, or vegetative cells (VC) (live or dead). Exposed mice were evaluated for changes in behavioral and physical symptoms, bacterial clearance, pulmonary granulocytes, and pulmonary and circulatory pyrogenic cytokines (interleukins (IL)-1β, IL-6 and tumor necrosis factor (TNF)-α), as well as acute phase biomarkers (fibrinogen and serum amyloid A). Except for some differences in clearance rates, no marked effects were observed in mice exposed to any spore at 10⁶ or 10⁷ colony forming units (cfu). In contrast, live Bc or Bt VCs (10⁵ or 10⁶?cfu) produced shock-like symptoms (lethargy, hunched appearance, ruffled fur, and respiratory distress), and 11–200-fold elevations in pyrogenic cytokines at 2-h post-exposure. In the study, 4-h effects included increased lethargy, ocular discharge, and 1.5–4-fold rise in circulatory acute phase markers, but no indications of recovery. Bs VC did not produce any changes in symptoms or biomarkers. After 2 or 4?h of exposure to dead VC, increases of only plasma IL-1β and TNF-α (4.6- and 12.4-fold, respectively) were observed. These findings demonstrate that purified spores produced no marked effects in mice compared to that of metabolically active bacteria. This early screening regime was successful in distinguishing the pathogenicity of the different Bacillus species, and might be useful for assessing the relative hazard potential of other biotechnology-related candidate strains.     

Silver nanoparticles toxicity effect on photosystem II photochemistry of the green alga Chlamydomonas reinhardtii treated in light and dark conditions

The inhibitory effect of silver nanoparticles (AgNPs) on photochemical reactions of photosynthesis was investigated using the green alga model Chlamydomonas reinhardtii. Algal cells were exposed to 1, 5, and 10?µmol?L^?1 of AgNPs under both light and dark conditions during 6?h. The rapid rise of chlorophyll a fluorescence and the fluorescence imaging system were employed to investigate the alteration of photosystem II (PSII) photochemical reactions and the associated electron transport activity. When algal cells were exposed to 5 and 10?µmol?L^?1 of AgNPs, our results showed the evidence of a structural deterioration of PSII reaction center, the alteration of the oxygen evolving complex and the inhibition of electron transport activity, which was stronger for AgNPs treatment under light exposure. Under these conditions, there was no activation of regulated photoprotective mechanisms against excess absorbed light-energy by the antenna system of the PSII complex. The highest deteriorating effect on the structural and functional integrity of PSII was observed for algal cells exposed 6?h in light condition to 10?µmol?L^?1 of AgNPs. Therefore, we provide valuable data in this study permitting to use photosynthetic-based fluorescence parameters for aquatic toxicological risk investigation of polluted water that may contain AgNP suspension.     

Toxicological studies of zinc oxide nanomaterials in rats

In this study, we have evaluated the ability of zinc oxide (ZnO) nanoparticles to induce pulmonary and extrapulmonary toxicities was examined in rats following intratracheal (IT) instillation. Lungs of rats were instilled IT with either phosphate-buffered saline (PBS)?+?1% Tween 80, ZnO nanoparticles, carbonyl iron or quartz particles at a dose of 1 or 5?mg?kg^?1 body weight. Following exposure, bronchoalveolar lavage (BAL) fluid, blood samples and organs including lung, liver, kidneys, heart, pancreas, and brain were collected at 24?h, 1 week, or 1 month of post instillation of nanoparticles and different parameters estimated to assess toxicity. BAL fluid was analyzed for lactate dehydrogenase (LDH) and alkaline phosphatase (ALP) to assess pulmonary toxicity. Exposures to ZnO or quartz particles produced transient dose-dependant increase in BAL fluid LDH and ALP activities at all post exposure periods. Blood samples were analyzed for the tissue damage biomarkers to assess extrapulmonary toxicity. Histopathological examination of lung, liver and kidneys revealed dose-dependent degeneration and necrosis which worsened at 1 week post-instillation periods but recovered at 1 month post instillation. Histopathological examination of rat pancreas, heart, and brain exposed to quartz or ZnO particles showed no marked changes. Data suggest the instillation of ZnO nanoparticles produced a greater pulmonary toxicity in rats comparable with quartz; and extrapulmonary toxicities of these ZnO nanoparticles might be due to translocation into liver and kidney.     

Induction of micronuclei in bone marrow cells and hepatotoxicity of one of the most common over-the-counter pyrethroid insecticide products in Nigeria

Increasing environmental pollution in the tropics is creating a breeding ground for mosquitoes, leading to increasingly frequent use of insecticides to combat home infestation of mosquitoes, the vector of malarial parasites. Household members are therefore more prone to aerosol exposure and subsequent health effects. We assessed the hepatotoxic and clastogenic effects in rats exposed to different levels of aerosols of one of the insecticides most commonly in used in Nigeria. There were significant (p?2 in the groups of rats exposed to the aerosols when compared with the control group. In addition, rats exposed to the insecticide aerosols have elevated activities of serum enzymes: γ-glutamyl transferase, aspartate amino transferase and alanine amino transferase, as well as number of micronuclei scored in the bone marrow, at levels that are significantly (p?相似文献   

Studies on factors affecting survival of nile fish in the Sudan. III. The effect of oxygen

Tilapia nilotica L. were exposed to different levels of ambient oxygen concentrations for 24 h periods. Nitrogen was bubbled through the water to reduced the oxygen concentration to the respective test level. When testing concentrations of oxygen between 2.5 and 0.4 ppm over 24 h periods of exposure, the median tolerance limits (TLM) over 24 h were attained at 1.41 ppm of oxygen.     

Toxicity of cadmium to Parachanna obscura : As evidenced by alterations in hematology,histology, and behavior

Fish of species Parachanna obscura are exposed to four concentrations of cadmium (Cd) (0.02, 0.06, 0.18, or 0.54?mg?L^?1). Acute toxicity test results after 96?h showed marked hematological, histological, and behavioral changes. Quantitative blood analysis revealed that white blood cell (WBC), packed cell volume (PCV), and platelets counts were linearly correlated with increasing Cd concentrations; however, blood haemoglobin (Hb) showed an inverse relationship, with higher Hb levels at lower Cd concentrations. Histological changes of the liver showed hepatic separation, bloody appearance, and deposition of a brownish-yellow substance, which increased with rising concentrations of metal. Behavioral changes observed included reduced activity, avoidance response, and deposition of a slimy-whitish film on the body of the fish, which increased with concentration and exposure time.     

Evaluation of the effect of antimicrobials in marine cultures,using the copepod Acartia tonsa as a bioindicator

Cultures of the copepod Acartia tonsa are used both in aquaculture and ecotoxicology studies. However, the cultivation of these crustaceans at high densities results in the proliferation of microorganisms that can affect the organisms of interest, leading to illness or death. Antimicrobials inhibit microbial growth and may favour the cultivated species, aiding the development of ecological studies. This study investigated the potential of antimicrobials (antibiotic + antifungal) to inhibit bacteria and fungi when applied to marine zooplankton cultures, using the copepod A. tonsa as a bioindicator of acute toxicity. Treatment with 0.025?g?L^?1 of penicillin G potassium + 0.08?g?L^?1 of streptomycin sulphate + 0.04?g?L^?1 of neomycin sulphate + 0.005?g?L^?1 of nystatin resulted in 95% bacterial inhibition (after 12?h of exposure); however, after this time, the inhibitory effect was lost. The antimicrobial combination tested in this study prevented colonisation by fungi until 168?h after exposure, without causing acute toxicity to A. tonsa. Thus, it has potential for use in marine cultures of less sensitive organisms.