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Sea surface temperatures (SSTs) derived from passive microwave (PMW) observations benefit global ocean and SST analyses because of their near-all-weather availability. Present PMW SSTs have a real aperture-limited spatial resolution in excess of 50 km, limiting the spatial fidelity with which SST features, reflecting ocean dynamics, can be captured. This contrasts with the target resolution of global analyses of 5 to 10 km. The Copernicus Imaging Microwave Radiometer (CIMR) is a mission concept under consideration as a high-priority candidate mission for the expansion of the Copernicus space programme. This instrument would be capable of real aperture resolution < 15 km with low total uncertainties in the range 0.4−0.8 K for channels between 1.4 and 36.5 GHz, and a dual-view arrangement that further reduces noise. This paper provides a comparative study of SST uncertainty and feature resolution with and without the availability of CIMR in the future SST-observing satellite constellation based on a detailed simulation of CIMR plus infrared observations and the processing of global SST analyses with 0.05° final grid resolution. Simulations of CIMR data including structured errors were added to an observing system consisting of the Sea and Land Surface Temperature Radiometer (SLSTR) on Sentinel-3A and the Advanced Very High Resolution Radiometer (AVHRR) on MetOp-A. This resulted in a large improvement in the global root-mean-square error (RMSE) for SST from 0.37 K to 0.21 K for January and 0.40 K to 0.25 K for July. There was a particularly noticeable improvement in the performance of the analysis, as measured by the reduction in RMSE, for dynamical and persistently cloudy areas. Of these, the Aghulas Current showed an improvement of 43% in January and 48% in July, the Gulf Stream showed 70% and 44% improvements, the Southern Ocean showed 57% and 74% improvements, and the Maritime Continent showed 50% and 40% improvements, respectively.

We present an analysis of information content for sea surface temperature (SST) retrieval from the Advanced Microwave Scanning Radiometer 2 (AMSR2). We find that SST uncertainty of ∼0.37 K can be achieved within an optimal estimation framework in the presence of wind, water vapour and cloud liquid water effects, given appropriate assumptions for instrumental uncertainty and prior knowledge, and using all channels. We test all possible combinations of AMSR2 channels and demonstrate the importance of including cloud liquid water in the retrieval vector. The channel combinations, with the minimum number of channels, that carry most SST information content are calculated, since in practice calibration error drives a trade-off between retrieved SST uncertainty and the number of channels used. The most informative set of five channels is 6.9 V, 6.9 H, 7.3 V, 10.7 V and 36.5 H and these are suitable for optimal estimation retrievals. We discuss the relevance of microwave SSTs and issues related to them compared to SSTs derived from infra-red observations.

The lipid affinity of plasma apolipoproteins is an important modulator of lipoprotein metabolism. Mutagenesis techniques have been widely used to modulate apolipoprotein lipid affinity for studying biological function, but the approach requires rapid and reliable lipid affinity assays to compare the mutants. Here, we describe a novel method that measures apolipoprotein binding to a standardized preparation of small unilamellar vesicles (SUVs) containing trace biotinylated and fluorescent phospholipids. After a 30 min incubation at various apolipoprotein concentrations, vesicle-bound protein is rapidly separated from free protein on columns of immobilized streptavidin in a 96-well microplate format. Vesicle-bound protein and lipid are eluted and measured in a fluorescence microplate reader for calculation of a dissociation constant and the maximum number of potential binding sites on the SUVs. Using human apolipoprotein A-I (apoA-I), apoA-IV, and mutants of each, we show that the assay generates binding constants that are comparable to other methods and is reproducible across time and apolipoprotein preparations. The assay is easy to perform and can measure triplicate binding parameters for up to 10 separate apolipoproteins in 3.5 h, consuming only 120 μg of apolipoprotein in total. The benefits and potential drawbacks of the assay are discussed.