Single-species flow-through toxicity tests were conducted to determine the times-to-death of two indigenous fish to South Florida--least killifish (Heterandria formosa) and mosquitofish (Gambusia affinis)--from acute exposure to endosulfan sulfate. Mortalities were recorded within 8-h periods from test initiation to termination at 96 h. The 96-h LC(50)s for least killifish and mosquitofish estimated using the trimmed-Spearman-Karber method were 2.0 and 2.3 microg/l, respectively. An accelerated failure time model was used to estimate times to death at selected concentrations. Data were fit to log-normal, log-logistic, and Weibull distributions. Acute toxicity data fit to the Weibull distribution produced a better relative fit than log-normal or log-logistic distributions for both toxicity tests. The survival-time profiles and associated statistics illustrate the benefit of considering exposure duration as well as concentration when predicting acute risk to species' populations. Both toxicity tests had similar outcomes from exposure to endosulfan sulfate, with least killifish being slightly more likely to die at lower concentrations and shorter time periods than mosquitofish. From the models generated by the toxicity tests, times-to-death for least killifish and mosquitofish were estimated for environmentally relevant concentrations of total endosulfan at a site of concern in South Florida. When the results from the current toxicity tests were compared to environmental concentrations from previous screening-level ecological risk assessments, the durations necessary to potentially kill 10% or more of the populations of the two native south Florida fish species were estimated to be 77 and 96 h for least killifish and mosquitofish, respectively. However, the exposure values included the alpha and beta isomers as well as endosulfan sulfate; therefore, an understanding of their toxicity might be important in understanding the survival dynamics of fish species in endosulfan sulfate-contaminated sites.
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http://dx.doi.org/10.1007/s00244-009-9415-7 | DOI Listing |
J Colloid Interface Sci
April 2025
State Key Laboratory of Pulp and Paper Engineering, South China University of Technology, Guangzhou 510640, China. Electronic address:
Conventional light-driven antimicrobial strategies of zinc oxide (ZnO) are limited by inadequate illumination in dark environments. In this study, carboxylated cellulose nanocrystals (MCNC) mediated flower-like ZnO (C@Z) with self-promoted reactive oxygen species release under dark is fabricated. The adsorption of Zn ions on MCNC prompts the growth of ZnO along the (002) crystal plane, forming a flower-like hybrid with superior dispersibility and oxygen vacancies compared to MCNC-free ZnO, which exposes the (100) plane.
View Article and Find Full Text PDFToxicon
January 2025
Faculty of Biological and Environmental Sciences, Federal University of Grande Dourados (UFGD), Dourados-Itahum Highway, Km 12 - Unit II, University City, 79804-970, Dourados, MS, Brazil; Faculty of Exact Sciences and Technology, Federal University of Grande Dourados (UFGD), Dourados-Itahum Highway, Km 12 - Unit II, University City, 79804-970, Dourados, MS, Brazil.
The venom of Ectatomma brunneum is considered promising for drugs development. Therefore, it is important to evaluate its toxic potential and genetic instability using biological assays. To this end, toxicity assays were performed with Artemia salina, cytotoxicity and genotoxicity with Allium cepa and mutagenicity with Ames.
View Article and Find Full Text PDFInt J Radiat Oncol Biol Phys
January 2025
The Royal Marsden NHS Foundation Trust, London SM2 5PT, UK; Radiotherapy and Imaging Division, Institute of Cancer Research, London SM2 5NG, UK.
Purpose: In the PACE-B study, a non-randomised comparison of toxicity outcomes between stereotactic body radiotherapy (SBRT) platforms revealed fewer urinary side-effects with CyberKnife (CK) compared to conventional linac (CL) SBRT. This analysis compares baseline characteristics and planning dosimetry between the CK-SBRT and CL-SBRT cohorts in PACE-B, aiming to provide insight into possible reasons for differing toxicity outcomes between the platforms.
Methods: Dosimetric parameters for the surrogate urethra (SU), contoured urethra, bladder, bladder trigone (BT), and rectum were extracted from available CT planning scans of PACE-B SBRT patients.
Bioorg Chem
January 2025
Laboratorio de Peptidos Bioactivos, Department of Organic Chemistry, Faculty of Biochemistry and Biological Sciences, National University of the Littoral, Ciudad Universitaria UNL, 3000 Santa Fe, Argentina; National Scientific and Technical Research Council (CONICET), Ministry of Science, Technology and Innovation, Godoy Cruz 2290, Ciudad de Buenos Aires, Argentina. Electronic address:
The search for novel cholinesterase inhibitors is essential for advancing treatments for neurodegenerative disorders such as Alzheimer's disease (AD). In this study, we employed the Rosetta pepspec module, originally developed for designing peptides targeting protein-protein interactions, to design de novo peptides targeting the peripheral aromatic site (PAS) of acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). A total of nine peptides were designed for human AChE (hAChE), T.
View Article and Find Full Text PDFFront Biosci (Landmark Ed)
January 2025
Department of Zoology, College of Science, King Saud University, 11451 Riyadh, Saudi Arabia.
Background: We investigated chitosan's protective effects against tertiary butylhydroquinone (TBHQ)-induced toxicity in adult male rats, focusing on cognitive functions and oxidative stress in the brain, liver, and kidneys.
Methods: Rats were divided into four groups (n = 8/group): (1) Control, (2) Chitosan only, (3) TBHQ only, and (4) Chitosan + TBHQ.
Results: TBHQ exposure led to significant cognitive impairments and increased oxidative stress, marked by elevated malondialdehyde (MDA) and decreased superoxide dismutase (SOD) and glutathione (GSH) levels.
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