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Hamilton, T. J.

Publications and source records attributed to Hamilton, T. J..

2 recordsLinked to original sources

Elevated environmental CO2 stimulates photosynthesis and induces differential oxidative responses in two Caribbean reef-building coral species

Reef-building corals maintain intracellular photosymbiosis with dinoflagellate algae, allowing them to use photosynthetic products as metabolic fuel. Carbon dioxide (CO2) is a key substrate for photosynthesis, but its rapid increase in the global ocean due to anthropogenic emissions (known as ocean acidification) may disrupt coral symbiosis. We examined the effects of elevated CO2 on photosynthetic O2 production, oxidative damage, and antioxidant systems in the Caribbean reef-building corals Porites astreoides and Orbicella franksi. Coral colonies collected at 3m depth in Bocas del Toro (Panama) were exposed to control (390 {micro}atm CO2, pH ~8.00) or elevated CO2 ({approx}1,060 {micro}atm CO2, pH {approx}7.70) conditions in outdoor flow-through aquaria for 10 days. Flowing seawater had higher O2O2 concentrations in elevated CO2 tanks, with the largest differences at higher irradiance. Microsensor measurements confirmed that acute and chronic exposure to elevated CO2 significantly stimulated photosynthetic O2 production in both species. Despite increased O2 production. neither species showed significant changes in lipid peroxidation, reduced glutathione, or superoxide dismutase, catalase, and glutathione-S-transferase activities. Protein oxidation was unchanged in O. franksi but significantly decreased in P. astreoides. These results are consistent with partial relief of carbon limitation in P. astreoides symbionts under elevated CO2, potentially improving photosynthetic efficiency and decreasing reactive oxygen species production. These findings support the resilience of P. astreoides to OA and suggest that elevated CO2 may increase daytime O2 levels on future reefs, with implications for the aerobic metabolism of reef organisms.

physiology↗

Neuromorphic Cytometry: Implementation on cell counting and size estimation

Flow cytometry is a widespread and high-throughput technology that can measure the features of cells and can be combined with fluorescence analysis for additional phenotypical characterisations but only provide low-dimensional output and spatial resolution. Imaging flow cytometry is another technology that offers rich spatial information, allowing more profound insight into single-cell analysis. However, offering such high-resolution, full-frame feedback can compromise speed and has become a significant trade-off challenge to tackle during development. In addition, the current dynamic range offered by conventional photosensors can only capture limited fluorescence signals, exacerbating the difficulties in elevating performance speed. Neuromorphic photo-sensing architecture focuses on the events of interest via individual-firing pixels to reduce data redundancy and provide low latency in data processing. With the inherent high dynamic range, this architecture has the potential to drastically elevate the performance in throughput by incorporating motion-activated spatial resolution. Herein, we presented an early demonstration of neuromorphic cytometry with the implementation of object counting and size estimation to measure 8 m and 15 m polystyrene-based microparticles and human monocytic cell line (THP-1). In this work, our platform has achieved highly consistent outputs with a widely adopted flow cytometer (CytoFLEX) in detecting the total number and size of the microparticles. Although the current platform cannot deliver multiparametric measurements on cells, future endeavours will include further functionalities and increase the measurement parameters (granularity, cell condition, fluorescence analysis) to enrich cell interpretation.

cell biology↗