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Abstract The hundreds of tidewater glaciers found in the Canadian Arctic Archipelago have the potential to enhance delivery of nutrients and other material to the surface ocean. Despite this, their influence on marine ecosystems, specifically phytoplankton, is poorly characterized. Here we developed and applied a quantitative mass spectrometry‐based approach to measure phytoplankton ribulose‐1,5‐bisphosphate carboxylase/oxygenase (Rubisco) concentrations to examine differences in productivity in glacierized and non‐glacierized marine systems in Jones Sound, Nunavut, within Inuit Nunangat. Comparisons to chloroplast 16S rRNA gene amplicon sequencing data suggested that these measurements detect the majority of Rubisco produced in Jones Sound. Because Rubisco catalyzes carbon fixation, we used these measurements to estimate total and group‐specific primary production potential, which were within the range of historical primary production measurements made using classical methods in this region. Our measurements also revealed that up to 2% of total protein in the water column is Rubisco, and that Rubisco concentrations are correlated with chlorophyll fluorescence, with maxima near the nitracline. Rubisco produced by diatom generaChaetocerosandThalassiosirawere higher in marine regions influenced by glaciers, while Rubisco fromMicromonas(Chlorophyta) was greater in non‐glacierized regions. This suggests that future climate scenarios may favor smaller phytoplankton groups, likeMicromonas, with consequences for food webs and carbon cycling. This study broadens our understanding of how tidewater glaciers will impact phytoplankton communities, now and in a warmer future, and lays the foundation for using this mass spectrometry‐based approach to quantify phytoplankton group‐specific carbon fixation potential in other marine regions. 

Abstract High‐latitude oceans experience strong seasonality where low light limits photosynthetic activity most of the year. This limitation is pronounced for algae within and underlying sea ice, and these algae are uniquely acclimated to low light levels. During spring melt, however, light intensity and daylength increase drastically, triggering blooms of ice algae that play important roles in carbon cycling and ecosystem productivity. How the algae acclimate to this dynamic and heterogeneous environment is poorly understood. Here, we measured¹⁴C‐carbon fixation rates, photophysiology, and ribulose 1,5‐bisphosphate carboxylase oxygenase (Rubisco) content of sea‐ice algae in coastal waters near the western Antarctic Peninsula during spring, ranging from a low‐light‐acclimated, bottom community to a light‐saturated bloom. Carbon fixation rates by sea‐ice algae were similar to other Antarctic sea‐ice measurements (2–49 mg C m⁻²d⁻¹), and there was little phytoplankton biomass in the underlying water at the time of sampling. Net‐to‐gross ratios of carbon fixation were generally high and showed no relationship with ice type. We found algal photophysiology and Rubisco concentrations varied in relation to the different types of ice, altering the balance between the photochemical and biochemical processes that constrain carbon fixation rates. For algae inhabiting the bottom layers of sea ice, rates of carbon fixation were largely constrained by light availability whereas in surface seawater, interior and rotten/brash ice, carbon fixation rates could be calculated with reasonable accuracy from measurements of Rubisco concentrations. This work provides additional insight and means to evaluate carbon fixation rates as sea ice continues to change in future. 

Abstract Seasonal cycles within the marginal ice zones in polar regions include large shifts in temperature and salinity that strongly influence microbial abundance and physiology. However, the combined effects of concurrent temperature and salinity change on microbial community structure and biochemical composition during transitions between seawater and sea ice are not well understood. Coastal marine communities along the western Antarctic Peninsula were sampled and surface seawater was incubated at combinations of temperature and salinity mimicking the formation (cold, salty) and melting (warm, fresh) of sea ice to evaluate how these factors may shape community composition and particulate metabolite pools during seasonal transitions. Bacterial and algal community structures were tightly coupled to each other and distinct across sea-ice, seawater, and sea-ice-meltwater field samples, with unique metabolite profiles in each habitat. During short-term (approximately 10-day) incubations of seawater microbial communities under different temperature and salinity conditions, community compositions changed minimally while metabolite pools shifted greatly, strongly accumulating compatible solutes like proline and glycine betaine under cold and salty conditions. Lower salinities reduced total metabolite concentrations in particulate matter, which may indicate a release of metabolites into the labile dissolved organic matter pool. Low salinity also increased acylcarnitine concentrations in particulate matter, suggesting a potential for fatty acid degradation and reduced nutritional value at the base of the food web during freshening. Our findings have consequences for food web dynamics, microbial interactions, and carbon cycling as polar regions undergo rapid climate change. 

Abstract Marine diatoms are key primary producers across diverse habitats in the global ocean. Diatoms rely on a biophysical carbon concentrating mechanism (CCM) to supply high concentrations of CO₂around their carboxylating enzyme, RuBisCO. The necessity and energetic cost of the CCM are likely to be highly sensitive to temperature, as temperature impacts CO₂concentration, diffusivity, and the kinetics of CCM components. Here, we used membrane inlet mass spectrometry (MIMS) and modeling to capture temperature regulation of the CCM in the diatomPhaeodactylum tricornutum (Pt). We found that enhanced carbon fixation rates byPtat elevated temperatures were accompanied by increased CCM activity capable of maintaining RuBisCO close to CO₂saturation but that the mechanism varied. At 10 and 18 °C, diffusion of CO₂into the cell, driven byPt’s ‘chloroplast pump’ was the major inorganic carbon source. However, at 18 °C, upregulation of the chloroplast pump enhanced (while retaining the proportion of) both diffusive CO₂and active HCO₃⁻uptake into the cytosol, and significantly increased chloroplast HCO₃⁻concentrations. In contrast, at 25 °C, compared to 18 °C, the chloroplast pump had only a slight increase in activity. While diffusive uptake of CO₂into the cell remained constant, active HCO₃⁻uptake across the cell membrane increased resulting inPtdepending equally on both CO₂and HCO₃⁻as inorganic carbon sources. Despite changes in the CCM, the overall rate of active carbon transport remained double that of carbon fixation across all temperatures tested. The implication of the energetic cost of thePtCCM in response to increasing temperatures was discussed. 

Summary Marine microalgae within seawater and sea ice fuel high‐latitude ecosystems and drive biogeochemical cycles through the fixation and export of carbon, uptake of nutrients, and production and release of oxygen and organic compounds. High‐latitude marine environments are characterized by cold temperatures, dark winters and a strong seasonal cycle. Within this environment a number of diverse and dynamic habitats exist, particularly in association with the formation and melt of sea ice, with distinct microalgal communities that transition with the season. Algal physiology is a crucial component, both responding to the dynamic environment and in turn influencing its immediate physicochemical environment. As high‐latitude oceans shift into new climate regimes the analysis of seasonal responses may provide insights into how microalgae will respond to long‐term environmental change. This review discusses recent developments in our understanding of how the physiology of high‐latitude marine microalgae is regulated over a polar seasonal cycle, with a focus on ice‐associated (sympagic) algae. In particular, physiologies that impact larger scale processes will be explored, with an aim to improve our understanding of current and future ecosystems and biogeochemical cycles. 

Synopsis Intense bottom-ice algal blooms, often dominated by diatoms, are an important source of food for grazers, organic matter for export during sea ice melt, and dissolved organic carbon. Sea-ice diatoms have a number of adaptations, including accumulation of compatible solutes, that allows them to inhabit this highly variable environment characterized by extremes in temperature, salinity, and light. In addition to protecting them from extreme conditions, these compounds present a labile, nutrient-rich source of organic matter, and include precursors to climate active compounds (e.g., dimethyl sulfide [DMS]), which are likely regulated with environmental change. Here, intracellular concentrations of 45 metabolites were quantified in three sea-ice diatom species and were compared to two temperate diatom species, with a focus on compatible solutes and free amino acid pools. There was a large diversity of metabolite concentrations between diatoms with no clear pattern identifiable for sea-ice species. Concentrations of some compatible solutes (isethionic acid, homarine) approached 1 M in the sea-ice diatoms, Fragilariopsis cylindrus and Navicula cf. perminuta, but not in the larger sea-ice diatom, Nitzschia lecointei or in the temperate diatom species. The differential use of compatible solutes in sea-ice diatoms suggests different adaptive strategies and highlights which small organic compounds may be important in polar biogeochemical cycles.