Home About us Contact
|
Home About us Contact | ||
|
|
||
Highest Toxicity (highest + toxicity)
Selected AbstractsAcute toxicity of fatty acids to the freshwater green alga Selenastrum capricornutumENVIRONMENTAL TOXICOLOGY, Issue 5 2003Yasushi Kamaya Abstract The acute toxicity of fatty acids (C14 to C18) commonly found in wood was determined by the standard algal growth inhibition test using the freshwater green alga Selenastrum capricornutum. Toxicity, quantified as IC50 values, varied depending on the number of total carbons and double bonds. Of the tested acids, oleic (cis -9-octadecenoic) acid showed the highest toxicity (72-h IC50 = 0.47 mg/L) to the alga, and triolein, a triglyceride of oleic acid, showed no apparent toxicity. Further examination of a series of C18:1 acids with a double bond at the 6, 11, or 12 position revealed that both double-bond position and cis or trans configuration affected toxicity. The 72-h IC50 data for these fatty acids and related compounds seemed to correlate well with the melting point (mp), showing two separate linear relationships: at mp < 35°C toxicity increased with increasing melting point, and at mp > 40°C toxicity decreased with melting point. © 2003 Wiley Periodicals, Inc. Environ Toxicol 18: 289,294, 2003. [source] Application of toxicity identification evaluation procedures for characterizing produced water using the tropical mysid, Metamysidopsis insularisENVIRONMENTAL TOXICOLOGY & CHEMISTRY, Issue 5 2004Najila Elias-Samlalsingh Abstract Toxicity identification evaluations (TIEs) were performed on seven produced water (PW) effluents from inland discharge facilities operated in Trinidad and Tobago, a Caribbean tropical country with one of the oldest commercial oil industries in the world. The research was performed to determine the presence and magnitude of toxicity and characterize which toxicants are responsible for observed effects. Marine effluent toxicity characterizations with Metamysidopsis insularis revealed high whole acute toxic-unit response for produced water ranged from 8.1 to >17.0 acute toxic-unit (initial toxicity test) and 5.7 to 1,111 acute toxic-unit (baseline toxicity test). Toxicity test results for all sites except one, which had the highest toxicity, are comparative with similar studies on produced water. The toxicological causality of this complex mixture differed for each PW with nonpolar organics being consistently toxic in all samples. Other potential toxicants contributing to overall toxicity to a much lesser extent were metals, ammonia, and volatile organic compounds. With the use of sodium thiosulfate and filtration manipulations for only PW6 sample, there was very slight reduction in toxicity; therefore, oxidants and filterable materials were not a great contributing factor. Whole effluent toxicity also can be attributed to ionic imbalance and the very stable oil-in-water emulsion that consists of fine oil droplets (less than 0.1,10 ,m with an average diameter of 2.5 ,m). This investigation is the first of its type in Trinidad and demonstrates clearly the applicability of this test method and local test species for evaluating complex effluents in tropical environments. [source] STUDIES ON SELECTIVE TOXICITY OF SIX INSECTICIDES BETWEEN GREEN PEACH APHID AND LADYBIRDSINSECT SCIENCE, Issue 2 2002XUE Ming Abstract, The selective toxicity of six kinds of insecticides, including imidacloprid, imidacloprid + synergist (SV1), fenvalerate, endosulfan, methomyl and dimethoate, between the green peach aphid (Myzus persicae Sulzer) and two species of ladybirds (Coccinella septempunctata Linnaeus and Propylaea japonica Thunbery), was investigated in the laboratory. The reults showed that both imidacloprid WP and imidacloprid + synergist (SVl) EC possessed the highest toxicity to the aphids. Between C. septempunctata and M. persicae and between P. japonica and M. persicae, the selective toxicity ratios (STRs) of imidacloprid WP, imidacloprid+ synergist (SV1) EC and endosulfan EC were 37.6 and 13.0, 9.84 and 7.75, 54.0 and 7.28 respectively. All of them showed rather high selective toxicity. The STRs of fenvalerate EC, dimethoate EC and methomyl EC were all very low, ranging from 0.02 to 0.21, indicating their low degree of safety to the two species of ladybids. The results demomarated that imidacloprid WP and imidacloprid + SVl EC not only had rather high toxicity to the aphids, but also reduced strikingly the reproduction rate and fecundity of the survival aphids. Insecticides can induce the relative fitness of insects decrease. Among the six insecticides tested with M. persicae, the following were insecticides and the order of induction was: imidacloprid + SV1 imidacloprid endosulfan methomyl fenvalerate > dimethoate. [source] A computational study of the carboxylic acid of phloroglucinol in vacuo and in water solutionINTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, Issue 3 2010Liliana Mammino Abstract 2,4,6-Trihydroxybenzoic acid (FA) is the carboxylic acid of phloroglucinol and, in turn, the parent compound of many biologically active compounds. The biological activities of FA are "extreme" among trihydroxybenzoic acids (e.g., lowest antioxidant activity, highest toxicity toward crustaceans). A complete MP2/6-31++G(d,p) conformational study in vacuo shows that the lowest energy conformers contain two intramolecular hydrogen bonds between the COOH function and the two ortho phenolic OH, with the Z form of COOH preferred over the E form. Comparisons with conformers in which the H-bonds are removed enable fairly reliable evaluations of their energy, because of an off-plane shift of COOH on H-bond removal, decreasing the effects of lone pair repulsion. Comparisons with the other hydroxybenzoic acids (extensively calculated in vacuo at the same level of theory) suggest that FA has the strongest intramolecular H-bonds. PCM calculations of FA in water solution show the same sequence of relative stabilities as in vacuo, with narrower differences because of the greater solvent stabilization of higher energy conformers. Calculations of adducts with water molecules H-bonded to different donor,acceptor centers of FA show the preferred arrangements of water molecules around the different regions of FA and confirm that the stronger intramolecular H-bonds are not broken on competition with the possibility of formation of intermolecular H-bonds. HF/6-31++G(d,p) calculations of adducts, in which the FA molecule is completely surrounded by water molecules, show that 14,16 water molecules (depending on the FA conformer geometry) realize arrangements corresponding to a presumable first solvation layer, with all the water molecules directly H-bonded to donor,acceptor centers of FA or bridging water molecules directly H-bonded to them. © 2009 Wiley Periodicals, Inc. Int J Quantum Chem, 2010 [source] | ||||||||||