This study analyzes relationships between concentration of suspended particles represented by dry mass, [SPM], or area, [AC], and optical properties including particulate beam attenuation (c p ), side scattering (b s ), and backscattering (b bp ), obtained from an intensive sampling program in coastal and offshore waters around Europe and French Guyana. First-order optical properties are driven by particle concentration with best predictions of [SPM] by b bp and b s , and of [AC] by c p . Second-order variability is investigated with respect to particle size, apparent density (dry weight-to-wet-volume ratio), and composition. Overall, the mass-specific particulate backscattering coefficient, b bp remains unexplained. Possible causes are the limitation of the measured size distributions to the 2-302-mm range and effects of particle shape and internal structure that affect b bp more than c p and were not accounted for.

Phytoplankton blooms in the Barents Sea are highly sensitive to seasonal and interannual changes in sea ice extent, water mass distribution, and oceanic fronts. With the ongoing increase of Atlantic Water inflows, we expect an impact on these blooms. Here, we use a state‐of‐the‐art collection of in situ hydrogeochemical data for the period 1998–2014, which includes ocean color satellite‐derived proxies for the biomass of calcifying and noncalcifying phytoplankton. Over the last 17 years, sea ice extent anomalies were evidenced having direct consequences for the spatial extent of spring blooms in the Barents Sea. In years of minimal sea ice extent, two spatially distinct blooms were clearly observed: one along the ice edge and another in ice‐free water. These blooms are thought to be triggered by different stratification mechanisms: heating of the surface layers in ice‐free waters and melting of the sea ice along the ice edge. In years of maximal sea ice extent, no such spatial delimitation was observed. The spring bloom generally ended in June when nutrients in the surface layer were depleted. This was followed by a stratified and oligotrophic summer period. A coccolithophore bloom generally developed in August, but was confined only to Atlantic Waters. In these same waters, a late summer bloom of noncalcifying algae was observed in September, triggered by enhanced mixing, which replenishes surface waters with nutrients. Altogether, the 17 year time‐series revealed a northward and eastward shift of the spring and summer phytoplankton blooms.