Abstract:Earth's polar regions are extreme ecosystems, marked by perennial darkness and seasonal mosaics of sea ice that modify the salinity, temperature, and incoming light of subsurface waters. Recent work in the Arctic has shown that phytoplankton can thrive underneath sea ice, dwarfing previous estimates for phytoplankton productivity across the annual cycle (Arrigo et al., 2012(Arrigo et al., , 2014Assmy et al., 2017), and raising questions of how sea ice influences under ice phytoplankton.The effects of sea ice o… Show more
“…Similar to previous work (DeVries & Weber, 2017; Siegel et al., 2014), limiting our reconstruction to regions with more complete satellite coverage leads to gaps in polar regions at times of the year characterized by significant sea ice coverage and pervasive light limitation (Siegel et al., 2002). Although based on in situ measurements some level of particle production is likely to occur in these regions and times of the year (e.g., Bisson & Cael, 2021; Lowry et al., 2018; Hague & Vichi, 2021), we lack both remote sensing and UVP5 observations that would allow robust estimates of particle abundance and size under such conditions. Future work should be devoted to closing these gaps.…”
Throughout the ocean surface, autotrophic organisms fix CO 2 and inorganic nutrients to produce organic matter, which accumulates in the water column as suspended particles (Falkowski et al., 1998). The fate of these particles in turn controls major oceanic biogeochemical cycles, and the ability of the ocean to sequester atmospheric
“…Similar to previous work (DeVries & Weber, 2017; Siegel et al., 2014), limiting our reconstruction to regions with more complete satellite coverage leads to gaps in polar regions at times of the year characterized by significant sea ice coverage and pervasive light limitation (Siegel et al., 2002). Although based on in situ measurements some level of particle production is likely to occur in these regions and times of the year (e.g., Bisson & Cael, 2021; Lowry et al., 2018; Hague & Vichi, 2021), we lack both remote sensing and UVP5 observations that would allow robust estimates of particle abundance and size under such conditions. Future work should be devoted to closing these gaps.…”
Throughout the ocean surface, autotrophic organisms fix CO 2 and inorganic nutrients to produce organic matter, which accumulates in the water column as suspended particles (Falkowski et al., 1998). The fate of these particles in turn controls major oceanic biogeochemical cycles, and the ability of the ocean to sequester atmospheric
“…GCMs used here are too coarse to resolve the complex boundary layer dynamics that result from surface melt processes of sea ice (Holland, 2003;Horvat et al, 2016;Pellichero et al, 2017), and thus, they are not suited for determining the convective state of the upper ocean in the presence of sea ice leads. Instead, we considered the ocean to be non-convecting if sea ice was melting at its base, which would lead to stratification of the upper ocean, consistent with Argo observations of high negative covariance between a shoaling MLD and increasing phytoplankton biomass under ice (Bisson and Cael, 2021).…”
Section: Cmip6 Datamentioning
confidence: 93%
“…In the Southern Ocean, annual sea ice coverage has changed less than in the Arctic over the satellite period (Parkinson, 2019), and sea ice is typically thinner, more seasonal, and more fragmented. Yet, studies have not yet described or quantified the potential for widespread UIBs under Antarctic sea ice, although observations from under-ice biogeochemical (BGC)-Argo floats (Arteaga et al, 2020;Hague and Vichi, 2021;Bisson and Cael, 2021) demonstrate that primary production may initiate before seasonal sea ice retreat, and even before the restratification of surface waters.…”
Section: Introductionmentioning
confidence: 99%
“…Our primary in situ evidence for sub-ice phytoplankton growth is particulate backscatter-derived phytoplankton carbon (PC) and chlorophyll-a (Chl-a) fluorescence. Chl-a is a pigment common to all phytoplankton, which is historically favored as a proxy for phytoplankton biomass, including in under-ice studies (Arrigo et al, 2010;Arrigo et al, 2014;Briggs et al, 2018;Ardyna et al, 2020;Bisson and Cael, 2021). Biomass and Chl-a may not always be directly connected because of mechanistic (i.e., photoacclimation, nutrient conditions, growth stage) and methodological biases (i.e., lamp source, target volume, or calibration standard) (Haëntjens et al, 2017;Johnson et al, 2017;Roesler et al, 2017).…”
Areas covered in compact sea ice were often assumed to prohibit upper-ocean photosynthesis. Yet, under-ice phytoplankton blooms (UIBs) have increasingly been observed in the Arctic, driven by anthropogenic changes to the optical properties of Arctic sea ice. Here, we show evidence that the Southern Ocean may also support widespread UIBs. We compile 77 time series of water column samples from biogeochemical Argo floats that profiled under compact (80%–100% concentration) sea ice in austral spring–summer since 2014. We find that that nearly all (88%) such measurements recorded increasing phytoplankton biomass before the seasonal retreat of sea ice. A significant fraction (26%) met a observationally determined threshold for an under-ice bloom, with an average maximum chlorophyll-a measurement of 1.13 mg/m3. We perform a supporting analysis of joint light, sea ice, and ocean conditions from ICESat-2 laser altimetry and climate model contributions to CMIP6, finding that from 3 to 5 million square kilometers of the compact-ice-covered Southern Ocean has sufficient conditions to support light-limited UIBs. Comparisons between the frequency of bloom observations and modeled bloom predictions invite future work into mechanisms sustaining or limiting under-ice phytoplankton blooms in the Southern Hemisphere.
“…Indeed, fractured, thick sea ice was found to support phytoplankton blooms [ 101 ] in May–June, months before seasonal sea ice retreat, and lateral variability in light conditions plays an important role in driving the availability of sunlight in the upper ocean [ 6 , 102 , 103 ]. In the Southern Ocean, the floe-like mosaic that extends across the sea ice zone has a lower concentration than the Arctic, which may permit phytoplankton growth under sea ice throughout the spring and summer that is challenging to observe remotely [ 75 , 104 ].…”
Marginal ice zones (MIZs) are qualitatively distinct sea-ice-covered areas that play a critical role in the interaction between the polar oceans and the broader Earth system. MIZ regions have high spatial and temporal variability in oceanic, atmospheric and ecological conditions. The salient qualitative feature of MIZs is their composition as a mosaic of individual floes that range in horizontal extent from centimetres to tens of kilometres. Thus the floe size distribution (FSD) can be used to quantitatively identify and describe them. Here, the history of FSD observations and theory, and the processes (particularly the impact of ocean waves) that determine floe sizes and size distribution, are reviewed. Coupled wave-FSD feedbacks are explored using a stochastic model for thermodynamic wave-sea-ice interactions in the MIZ, and some of the key open questions in this rapidly growing field are discussed.
This article is part of the theme issue ‘Theory, modelling and observations of marginal ice zone dynamics: multidisciplinary perspectives and outlooks’.
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