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Ross-Nickoll, M.

Publications and source records attributed to Ross-Nickoll, M..

3 recordsLinked to original sources

Temperature-dependence of Early Development of Zebrafish and the Consequences for Laboratory Use and Animal Welfare

Zebrafish (Danio rerio) are widely used in biological research, but the impact of incubation temperatures on developmental endpoints is still insufficiently studied. This study quantifies developmental differences in zebrafish embryos incubated at 26{degrees}C and 28{degrees}C, focusing on key endpoints (heartbeat onset, hatching time, eye size, yolk sac consumption, and body length). For this purpose, we recorded a high-resolution time series comprising hourly observations of early developmental stages and key events and bi-hourly observations of body length until 120 hours post fertilization. Additionally, we recorded a low-resolution time series at 72, 96, and 119 hours post fertilization for detailed measurements of eye size, yolk sac area, and body length. Embryos incubated at 26{degrees}C showed consistent delays in developmental stages compared to those at 28{degrees}C, with delays becoming more pronounced at later stages. Yolk sac consumption was delayed by about 19.8 hours at 26{degrees}C by 119 hours post fertilization, suggesting a delayed onset of independent feeding. These findings suggest that time-based regulatory limits for rearing zebrafish, such as the 120-hour threshold in German regulations (TierSchVerV), do not fully account for temperature-dependent development. The results emphasize the need for guidelines linking incubation temperatures to developmental progress. Summary StatementThis study highlights the impact of differences in incubation temperatures around the optimum (26 and 28{degrees}C) on zebrafish development. Results suggest reevaluation of animal welfare guidelines for temperature dependency.

developmental biology↗

Dataset on Temperature Dependency of Zebrafish Early Development

Zebrafish (Danio rerio) early development stages that do not feed independently, are classified as non-protected life stages under EU Directive 2010/63. Zebrafish reach the independently feeding stage not earlier than 120 hours post fertilization, depending on the incubation temperature. This paper presents a dataset documenting zebrafish early development at two commonly used temperatures 26 {degrees}C and 28 {degrees}C. We recorded onset of heartbeat and hatching as well as body length, eye size, yolk sac consumption, and swim bladder inflation. Additionally, locomotor activity was tracked after 96 and 119 hours post fertilization. The dataset serves as a baseline for selecting appropriate experimental conditions and optimizing toxicological study designs. They also facilitate the comparison of experimental results that were recorded at different temperatures. Furthermore, the data provide empirical evidence for amending current guidelines for tests with zebrafish embryos, in particular moving away from a rigid 120 hours post fertilization maximum test duration towards a temperature-dependent maximum test duration that is still in line with the aims of the German Animal Welfare Act.

developmental biology↗

Air-liquid interface exposure of A549 human lung cells to characterize the hazard potential of a gaseous bio-hybrid fuel blend

Gaseous and semi-volatile organic compounds emitted by the transport sector contribute to air pollution and have adverse effects on human health. To reduce harmful effects to the environment as well as to humans, renewable and sustainable bio-hybrid fuels are explored and investigated in the cluster of excellence "The Fuel Science Center" at RWTH Aachen University. However, data on the effects of bio-hybrid fuels on human health is scarce, leaving a data gap regarding their hazard potential. To help close this data gap, this study investigates potential toxic effects of a Ketone-Ester-Alcohol-Alkane (KEAA) fuel blend on A549 human lung cells. Experiments were performed using a commercially available air-liquid interface exposure system which was optimized beforehand. Then, cells were exposed at the air-liquid interface to 50-2000 ppm C3.7 of gaseous KEAA for 1 h. After a 24 h recovery period in the incubator metabolic activity and cytotoxicity of cells were assessed. Our data support the international occupational exposure limits of the single KEAA constituents and moreover indicate no adverse effect to A549 cells when exposed to a fuel mixture. This finding applies only to the exposure scenario tested in this study and is difficult to extrapolate to the complex in vivo situation.

pharmacology and toxicology↗