Search bioRxiv⌕ Search

Biology subjects

McLeod, A.

Publications and source records attributed to McLeod, A..

2 recordsLinked to original sources

Integrating ecosystem and contaminant models to predict the effects of ecosystem fluxes on contaminant dynamics

Pollution is one of the major drivers of ecosystem change in the Anthropocene. Toxic chemicals are not constrained to their source of origin as they cross ecosystem boundaries via biotic (e.g., animal migration) and abiotic (e.g., water flow) vectors. Meta-ecology has led to important insights on how spatial flows or subsidies of matter across ecosystem boundaries can have broad impacts on local and regional ecosystem dynamics but has not yet addressed the dynamics of pollutants. Understanding how these meta-ecosystem processes on contaminant dynamics may reverberate up a food chain is important even if they might be difficult to predict. Here we derive a modelling framework to predict how spatial ecosystem fluxes can influence contaminant dynamics and how the severity of this impact is dependent on the type of ecosystem flux leading to the spatial coupling (e.g., herbivore movement vs abiotic chemical flows). We mix an analytical and numerical approach to analyze our integrative model which couples two distinct sub-components - an ecosystem model and a contaminant model. We observe an array of dynamics for how chemical concentrations change with increasing nutrient input and loss rate across trophic levels. When we tailor our range of chemical parameter values to specific organic chemicals our results demonstrate that increasing nutrient input rates can lead to trophic dilution in pollutants such as polychlorinated biphenyls across trophic levels. Yet, increasing nutrient loss rate causes an increase in concentrations of chemicals across all trophic levels. A sensitivity analysis demonstrates that nutrient recycling is an important ecosystem process impacting contaminant concentrations, generating predictions to be addressed by future empirical studies. Importantly, our model demonstrates the utility of our framework for identifying drivers of contaminant dynamics in connected ecosystems including the importance that a) ecosystem processes, and b) movement, especially movement of lower trophic levels, have on contaminant concentrations. For example, how increasing nutrient loss rate leads to increasing contaminant concentrations, or how movement of lower trophic levels contributes to elevated herbivore contaminant concentrations. This dynamic is particularly relevant given that the flow of matter between ecosystems also serves as a vector for the transport of contaminants.

ecology↗

Quantitative Action Spectroscopy Reveals ARPE-19 Sensitivity to Long-Wave Ultraviolet Radiation at 350 nm and 380 nm

The role of ultraviolet radiation (UVR) exposure in the pathology of age-related macular degeneration (AMD) has been debated for decades with epidemiological evidence failing to find a clear consensus for or against it playing a role. A key reason for this is a lack of foundational research into the response of living retinal tissue to UVR in regard to AMD-specific parameters of tissue function. We therefore explored the response of cultured retinal pigmented epithelium (RPE), the loss of which heralds advanced AMD, to specific wavelengths of UVR across the UV-B and UV-A bands found in natural sunlight. Using a bespoke in vitro UVR exposure apparatus coupled with bandpass filters we exposed the immortalised RPE cell line, ARPE-19, to 10nm bands of UVR between 290 and 405nm. Physical cell dynamics were assessed during exposure in cells cultured upon specialist electrode culture plates which allow for continuous, non-invasive electrostatic interrogation of key cell parameters during exposure such as monolayer coverage and tight-junction integrity. UVR exposures were also utilised to quantify wavelength-specific effects using a rapid cell viability assay and a phenotypic profiling assay which was leveraged to simultaneously quantify intracellular reactive oxygen species (ROS), nuclear morphology, mitochondrial stress, epithelial integrity and cell viability as part of a phenotypic profiling approach to quantifying the effects of UVR. Electrical impedance assessment revealed unforeseen detrimental effects of UV-A, beginning at 350nm, alongside previously demonstrated UV-B impacts. Cell viability analysis also highlighted increased effects at 350nm as well as 380nm. Effects at 350nm were further substantiated by high content image analysis which highlighted increased mitochondrial dysfunction and oxidative stress. We conclude that ARPE-19 cells exhibit a previously uncharacterised sensitivity to UV-A radiation, specifically at 350nm and somewhat less at 380nm. If upheld in vivo, such sensitivity will have impacts upon geoepidemiological risk scoring of AMD.

pharmacology and toxicology↗