ABSTRACT
The Southern Ocean is a major sink of anthropogenic CO2 and an important foraging area for top trophic level consumers. However, iron limitation sets an upper limit to primary productivity. Here we report on a considerably dense late summer phytoplankton bloom spanning 9000 km2 in the open ocean of the eastern Weddell Gyre. Over its 2.5 months duration, the bloom accumulated up to 20 g C m-2 of organic matter, which is unusually high for Southern Ocean open waters. We show that, over 1997-2019, this open ocean bloom was likely driven by anomalies in easterly winds that push sea ice southwards and favor the upwelling of Warm Deep Water enriched in hydrothermal iron and, possibly, other iron sources. This recurring open ocean bloom likely facilitates enhanced carbon export and sustains high standing stocks of Antarctic krill, supporting feeding hot spots for marine birds and baleen whales.
Subject(s)
Ecosystem , Food Chain , Wind , Iron , Phytoplankton , Antarctic Regions , Oceans and SeasABSTRACT
Underwater light field characterization is of importance for understanding biogeochemical processes and heat budget of the global oceans, which are impacting and reacting to climate change. Vibrational Raman Scattering (VRS) was retrieved from backscattered radiances measured by three different hyperspectral satellite sensors, SCIAMACHY, GOME-2, and OMI, using Differential Optical Absorption Spectroscopy (DOAS). Diffuse attenuation coefficient (Kd) in the blue spectral range (390 to 426 nm) was derived from the VRS signal via a look-up-table established through ocean-atmosphere coupled radiative transfer modeling. We processed one year of data, representative of the overlapping period of optimal operation for all three sensors. Resulting data sets were evaluated by comparison with Kd at 490 nm from Ocean Colour Climate Change Initiative (OC-CCI) which was first converted to Kd at 390 to 426 nm. Good agreement with the OC-CCI Kd product was achieved for all three sensors when Kd was limited to below 0.15 m-1. Differences among the hyperspectral sensors and to OC-CCI were attributed to particular instrumental effects on the DOAS retrieval leading to temporal and spatial biases. This is in addition to the fact that the spatial and temporal resolution of the hyperspectral sensors data differ among themselves and are much lower then for the OC-CCI Kd-product. Further corrections (e.g., empirical) are necessary before these data sets can be merged in order to obtain a long-term Kd product for the blue spectral range.
ABSTRACT
Satellite remote sensing of chlorophyll a concentration (Chl-a) in the Arctic Ocean is spatially and temporally limited and needs to be supplemented and validated with substantial volumes of in situ observations. Here, we evaluated the capability of obtaining highly resolved in situ surface Chl-a using underway spectrophotometry operated during two summer cruises in 2015 and 2016 in the Fram Strait. Results showed that Chl-a measured using high pressure liquid chromatography (HPLC) was well related (R2 = 0.90) to the collocated particulate absorption line height at 676 nm obtained from the underway spectrophotometry system. This enabled continuous surface Chl-a estimation along the cruise tracks. When used to validate Chl-a operational products as well as to assess the Chl-a algorithms of the aqua moderate resolution imaging spectroradiometer (MODIS-A) and Sentinel-3 Ocean Land Color Imager (OLCI) Level 2 Chl-a operational products, and from OLCI Level 2 products processed with Polymer atmospheric correction algorithm (version 4.1), the underway spectrophotometry based Chl-a data sets proved to be a much more sufficient data source by generating over one order of magnitude more match-ups than those obtained from discrete water samples. Overall, the band ratio (OCI, OC4) Chl-a operational products from MODIS-A and OLCI as well as OLCI C2RCC products showed acceptable results. The OLCI Polymer standard output provided the most reliable Chl-a estimates, and nearly as good results were obtained from the OCI algorithm with Polymer atmospheric correction method. This work confirms the great advantage of the underway spectrophotometry in enlarging in situ Chl-a data sets for the Fram Strait and improving satellite Chl-a validation and Chl-a algorithm assessment over discrete water sample analysis in the laboratory.
