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Strobilurin fungicides are widely used pesticides in the world. They can have toxic effects not only to target organisms, but also to nontarget organisms. To assess their ecological risk, species sensitivity distributions (SSDs) are required for the development of water quality criteria (WQC). In this paper, the acute toxicity of four methoxyacrylate fungicides were experimentally determined and evaluated at 24, 48, 72 and 96 h for the species of Rana chensinensis and Limnodrilus hoffmeisteri , respectively. Acute and chronic HC 5 (5% hazard concentration) values and WQC values were calculated from SSDs based on the toxicity values determined in this paper and compiled from literature. SSDs revealed that aquatic animals were relatively sensitive species and aquatic plants are insensitive species for the four fungicides. However, different orders of species sensitivity in the acute and chronic toxicity indicated that these four fungicides had different toxic mechanisms or mode of action (MOA) to different species. According to toxicity correlation and principal component analysis (PCA), the kresoxim-methyl toxicity was very close to trifloxystrobin as compared with others due to that they are neutral compounds with very similar physicochemical properties. Quantitative structure-activity relationship (QSAR) revealed that toxicity of strobilurin fungicides were dependent both on chemical hydrophobicity and hydrogen bond basicity. These two molecular descriptors reflect the bio-uptake process and interaction of compounds with target receptors in an organism. WQC values and interspecies correlation are valuable for assessing water quality and understanding toxic mechanisms to different species. [Display omitted] • Acute toxicity of four fungicides have been determined and evaluated at 24, 48, 72 and 96 h. • Water quality criteria of acute and chronic toxicity have been developed for four strobilurin fungicides. • Toxicity of strobilurin fungicides is related with chemical hydrophobicity and hydrogen bonding potential. • The toxicity of four fungicides is not only dependent on the species, but also on the chemical structure. • Kresoxim-methyl toxicity is significantly related to trifloxystrobin toxicity because of their similar structure. [ABSTRACT FROM AUTHOR]

Although modes of action (MOAs) play a key role in the understanding of the toxic mechanism of chemicals, the MOAs have not been investigated for antibiotics to green algae. This paper is to discriminate excess toxicity from baseline level and investigate the MOAs of 13 different antibiotics to algae by using the determined toxicity values. Comparison of the toxicities shows that the inhibitors of protein synthesis to bacteria, such as azithromycin, doxycycline, florfenicol and oxytetracycline, exhibit significantly toxic effects to algae. On the other hand, the cell wall synthesis inhibitors, such as cefotaxime and amoxicillin, show relatively low toxic effects to the algae. The concentrations determined by HPLC indicate that quinocetone and amoxicillin can be easily photodegraded or hydrolyzed during the toxic tests. The toxic effects of quinocetone and amoxicillin to the algae are attributed to not only their parent compounds, but also their metabolites. Investigation on the mode of action shows that, except rifampicin, all the tested antibiotics exhibit excess toxicity to Pseudokirchneriella subcapitata ( P. subcapitata) . These antibiotics can be identified as reactive modes of action to the algae. They act as electrophilic mechanism of action to P. subcapitata . These results are valuable for the understanding of the toxic mechanism to algae. [ABSTRACT FROM AUTHOR]

The toxic effect can be affected by pH in water through affecting the degree of ionization of ionizable compounds. Wrong classification of mode of action can be made from the apparent toxicities. In this paper, the toxicity data of 61 compounds to Daphnia magna determined at three pH values were used to investigate the effect of pH on the discrimination of excess toxicity. The results show that the apparent toxicities are significantly less than the baseline level. Analysis on the effect of pH on bioconcentration factor (BCF) shows that the log BCF values are significantly over-estimated for the strongly ionizable compounds, leading to the apparent toxicities greatly less than the baseline toxicities and the toxic ratios greatly less than zero. A theoretical equation between the apparent toxicities and pH has been developed basing on the critical body residue (CBR). The apparent toxicities are non-linearly related to pH, but linearly to fraction of unionized form. The determined apparent toxicities are well fitted with the toxicities predicted by the equation. The toxicities in the unionized form calculated from the equation are close to, or greater than the baseline level for almost all the strongly ionizable compounds, which are very different from the apparent toxicities. The studied ionizable compounds can be either classified as baseline, less inert or reactive compounds in D. magna toxicity. Some ionizable compounds do not exhibit excess toxicity at a certain pH, due not to their poor reactivity with target molecules, but because of the ionization in water. [ABSTRACT FROM AUTHOR]