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Biology subjects

Martynek, M. P.

Publications and source records attributed to Martynek, M. P..

2 recordsLinked to original sources

Decadal tracking reveals species-specific limits to coral thermal acclimatization

Mass coral bleaching events driven by marine heatwaves are increasing in frequency and severity, yet the long-term recovery trajectories of surviving corals remain poorly understood. Here, leveraging a cohort of individual coral colonies with a decade of tracked environmental and bleaching history, we captured structural shifts in the coral thermal performance landscape. Specifically, we quantified thermal performance curves (TPCs) for photosynthesis and calcification in bleaching-resistant and bleaching-susceptible colonies of two ecologically dominant reef-building corals (Montipora capitata and Porites compressa) at four and six years following the 2019 marine heatwave in K[a]neohe Bay, Hawaii (2023 and 2025, respectively). Coral thermal performance shifted substantially between 2023 and 2025, and these shifts differed between species, bleaching phenotypes, and traits. In P. compressa, photosynthetic thermal optimum (Topt) shifted downward over time by 1.6{degrees}C across both phenotypes, suggesting recalibration toward prevailing conditions at the potential cost of future heat tolerance. In M. capitata, photosynthetic performance was lower in bleaching-susceptible corals in 2023 but converged by 2025, suggesting susceptible colonies recovered. In contrast, Topt of photosynthesis remained persistently higher in bleaching-resistant colonies, likely reflecting established symbiont communities. Critically, photosynthesis and calcification did not recover in parallel. Calcification TPCs for both phenotypes of M. capitata were stable across both timepoints, whereas calcification TPCs in P. compressa continued to change through 2025. These findings demonstrate that coral thermal performance is not static following heatwaves but continues to be reshaped over multi-year recovery periods, and that species-specific traits and strategies can fundamentally constrain the pace and coupling of physiological recovery. Furthermore, elevated thermal tolerance acquired through a heatwave can erode during prolonged periods of ambient temperatures. As recurrent bleaching events shorten recovery windows, understanding these dynamic physiological trajectories are essential for understanding and forecasting reef futures.

physiology↗

Heat stress disrupts acid-base homeostasis independent of symbiosis in the model cnidarian Exaiptasia diaphana

Heat stress threatens the survival of symbiotic cnidarians by causing their photosymbiosis to break down in a process known as bleaching. The direct effects of temperature on cnidarian host physiology remain difficult to describe because heat stress depresses symbiont performance, leading to host stress and starvation. The symbiotic sea anemone Exaiptasia diaphana provides an opportune system in which to disentangle direct vs. indirect effects of heat stress on the host, since it can survive indefinitely without symbionts. Here, we tested the hypothesis that heat stress directly influences cnidarian physiology by comparing symbiotic and aposymbiotic individuals of a clonal strain of E. diaphana. We exposed anemones to a range of temperatures (ambient, +2{degrees}C, +4{degrees}C, +6{degrees}C) for 15-18 days, then measured their symbiont population densities, autotrophic carbon assimilation and translocation, photosynthesis, respiration, and host intracellular pH (pHi). Anemones with initially high symbiont densities experienced dose-dependent symbiont loss with increasing temperature, resulting in a corresponding decline in host photosynthate accumulation. In contrast, anemones with low initial symbiont densities did not lose symbionts or assimilate less photosynthate as temperature increased, similar to the response of aposymbiotic anemones. Interestingly, pHi decreased in anemones at higher temperatures regardless of symbiont presence, cell density, or photosynthate translocation, indicating that heat stress disrupts cnidarian acid-base homeostasis independent of symbiosis dysfunction, and that acid-base regulation may be a critical point of vulnerability for hosts of this vital mutualism. Summary StatementWarming oceans threaten marine invertebrates. We found that heat disrupts acid-base homeostasis in a model symbiotic sea anemone regardless of symbiont presence or function, highlighting bleaching-independent effects of climate change.

physiology↗