Photoacclimation was studied in Thalassiosira pseudonana to help understand mechanisms underlying the success of diatoms in low-light environments, such as coastal and deep mixing ecosystems. Light harvesting and other cell characteristics were combined with oxygen and carbon production measurements to assess the water-splitting reaction at PSII ([Formula: see text]) and intermediate steps leading to net carbon production (NPPC). These measurements revealed that T. pseudonana is remarkably efficient at converting harvested light energy into biomass, with at least 57 % of [Formula: see text] retained as NPPC across all light-limited growth rates examined. Evidence for upregulation of ATP generation pathways that circumvent carbon fixation indicated that high growth efficiency at low light levels was at least partly due to increases in the efficiency of ATP production. Growth rate-dependent demands for ATP and NADPH were reflected in carbon composition and in unexpected shifts in the light-limited slope (α) of photosynthesis-irradiance relationships generated from chlorophyll-specific (14)C-uptake. Overall, these results suggest that pathway gating of carbon and energy flow depends on light availability and is a key factor promoting the efficiency of diatom growth at low light intensities.

Summary Symbiodiniaceae are a diverse family of marine dinoflagellates, well known as coral endosymbionts. Isolation and in vitro culture of Symbiodiniaceae strains for physiological studies is a widely adopted tool, especially in the context of understanding how environmental stress perturbs Symbiodiniaceae cell functioning. While the bacterial microbiomes of corals often correlate with coral health, the bacterial communities co‐cultured with Symbiodiniaceae isolates have been largely overlooked, despite the potential of bacteria to significantly influence the emergent physiological properties of Symbiodiniaceae cultures. We examined the physiological response to heat stress by Symbiodiniaceae isolates (spanning three genera) with well‐described thermal tolerances, and combined these observations with matched changes in bacterial composition and abundance through 16S rRNA metabarcoding. Under thermal stress, there were Symbiodiniaceae strain‐specific changes in maximum quantum yield of photosystem II (proxy for health) and growth rates that were accompanied by changes in the relative abundance of multiple Symbiodiniaceae‐specific bacteria. However, there were no Symbiodiniaceae‐independent signatures of bacterial community reorganisation under heat stress. Notably, the thermally tolerant Durusdinium trenchii (ITS2 major profile D1a) had the most stable bacterial community under heat stress. Ultimately, this study highlights the complexity of Symbiodiniaceae‐bacteria interactions and provides a first step towards uncoupling their relative contributions towards Symbiodiniaceae physiological functioning.

The ability to quantify spatio-temporal variability in phytoplankton growth and productivity is essential to improving our understanding of global carbon dynamics and trophic energy flow. Satellite-based observations offered the first opportunity to estimate depth-integrated net primary production (NPP) at a global scale, but early modeling approaches could not effectively address variability in algal physiology, particularly the effects of photoacclimation on changes in cellular chlorophyll. Here, a previously developed photoacclimation model was used to derive depth-resolved estimates of phytoplankton division rate (µ) and NPP. The new approach predicts NPP values that closely match discrete measurements of 14 C-based NPP and effectively captured both spatial and temporal variability observed during the four field campaigns of the North Atlantic Aerosols and Marine Ecosystems Study (NAAMES). We observed favorable growth conditions for phytoplankton throughout the annual cycle in the subtropical western North Atlantic. As a result, high rates of µ are sustained year-round resulting in a strong coupling between growth and loss processes and a more moderate spring bloom compared to the high-latitude subarctic region. Considerable light limitation was observed in the subarctic province during the winter, which resulted in divergent growth dynamics, stronger decoupling from grazing pressure and a taxonomically distinct phytoplankton community. This study demonstrates how detailed knowledge of phytoplankton division rate furthers our understanding of global carbon cycling by providing insight into the resulting influence on phytoplankton taxonomy and the loss processes that dictate the fate of fixed carbon.

Marine phytoplankton, and in particular diatoms, are responsible for almost half of all primary production on Earth. Diatom species thrive from polar to tropical waters and across light environments that are highly complex to relatively benign, and so have evolved highly divergent strategies for regulating light capture and utilization. It is increasingly well established that diatoms have achieved such successful ecosystem dominance by regulating excitation energy available for generating photosynthetic energy via highly flexible light harvesting strategies. However, how different light harvesting strategies and downstream pathways for oxygen production and consumption interact to balance excitation pressure remains unknown. We therefore examined the responses of three diatom taxa adapted to inherently different light climates (estuarine Thalassioisira weissflogii, coastal Thalassiosira pseudonana and oceanic Thalassiosira oceanica) during transient shifts from a moderate to high growth irradiance (85 to 1200 μmol photons m-2 s-1). Transient high light exposure caused T. weissflogii to rapidly downregulate PSII with substantial nonphotochemical quenching, protecting PSII from inactivation or damage, and obviating the need for induction of O2 consuming (light-dependent respiration, LDR) pathways. In contrast, T. oceanica retained high excitation pressure on PSII, but with little change in RCII photochemical turnover, thereby requiring moderate repair activity and greater reliance on LDR. T. pseudonana exhibited an intermediate response compared to the other two diatom species, exhibiting some downregulation and inactivation of PSII, but high repair of PSII and induction of reversible PSII nonphotochemical quenching, with some LDR. Together, these data demonstrate a range of strategies for balancing light harvesting and utilization across diatom species, which reflect their adaptation to sustain photosynthesis under environments with inherently different light regimes.

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