Seasonal and Long-Term Variability of Coccolithophores in the Black Sea According to Remote Sensing Data and the Results of Field Investigations

Based on satellite data from the SeaWiFS, MODIS-Aqua, and MODIS-Terra scanners, the long-term dynamics of coccolithophores in the Black Sea and their large-scale heterogeneity have been studied. During the twenty years in May and June, mass development of coccolithophores population of different intensities was recorded annually. Summer blooms of coccolithophores reached peak levels in 2006, 2012, and 2017, after abnormally cold winters. It was noted that in conditions of low summer temperatures, the blooming of coccolithophores could be significantly reduced or acquire a local character (2004). In the anomalous cold summer of 2001, coccolithophore blooms was replaced by the mass growth of diatoms. Over twenty years, numerous signs of coccolithophores mass development in the cold season have been revealed. Winter blooms develop mainly in warm winters with periods of low wind activity. The formation of a thermocline and the surface layer’s stability are essential factors for initiating winter blooms of coccolithophores. It was noted that after the winter blooms of coccolithophores, their summer growth was poorly expressed. It is shown that during periods of rapid growth, the bulk of coccolithophores is concentrated in the upper mixed layer and thermocline. During the blooming period, the share of coccolithophores in phytoplankton biomass constituted 70–85%. The intensity of coccolithophore’s blooms is associated with the previous diatoms’ growth level. The effect of eddies circulation on the distribution and growth of coccolithophores is considered

Seasonal and Long-Term Variability of Coccolithophores in the Black Sea According to Remote Sensing Data and the Results of Field Investigations

Based on satellite data from the SeaWiFS, MODIS-Aqua, and MODIS-Terra scanners, the long-term dynamics of coccolithophores in the Black Sea and their large-scale heterogeneity have been studied. During the twenty years in May and June, mass development of coccolithophores population of different intensities was recorded annually. Summer blooms of coccolithophores reached peak levels in 2006, 2012, and 2017, after abnormally cold winters. It was noted that in conditions of low summer temperatures, the blooming of coccolithophores could be significantly reduced or acquire a local character (2004). In the anomalous cold summer of 2001, coccolithophore blooms was replaced by the mass growth of diatoms. Over twenty years, numerous signs of coccolithophores mass development in the cold season have been revealed. Winter blooms develop mainly in warm winters with periods of low wind activity. The formation of a thermocline and the surface layer’s stability are essential factors for initiating winter blooms of coccolithophores. It was noted that after the winter blooms of coccolithophores, their summer growth was poorly expressed. It is shown that during periods of rapid growth, the bulk of coccolithophores is concentrated in the upper mixed layer and thermocline. During the blooming period, the share of coccolithophores in phytoplankton biomass constituted 70–85%. The intensity of coccolithophore’s blooms is associated with the previous diatoms’ growth level. The effect of eddies circulation on the distribution and growth of coccolithophores is considered

Elemental Composition of Particulate Matter in the Euphotic and Benthic Boundary Layers of the Barents and Norwegian Seas

The increasing influence of Atlantic inflows in the Arctic Ocean in recent decades has had a potential impact on regional biogeochemical cycles of major and trace elements. The warm and salty Atlantic water, entering the Eurasian Basin through the Norwegian Sea margin and the Barents Sea, affects particle transport, sink, phyto-, and zooplankton community structure and could have far-reaching consequences for the marine ecosystems. This study discusses the elemental composition of suspended particulate matter and fluffy-layer suspended matter derived from samples collected in the Barents Sea and northern Norwegian Sea in August 2017. The mosaic distribution of SPM elemental composition is mainly determined by two factors: (i) The essential spatial variability of biological processes (primary production, abundance, and phytoplankton composition) and (ii) differences in the input of terrigenous sedimentary matter to the sea area from drainage sources (weak river runoff, melting of archipelago glaciers, etc.). The distribution of lithogenic, bioessential, and redox-sensitive groups of elements in the particulate matter was studied at full-depth profiles. Marine cycling of strontium in the Barents Sea is shown to be significantly affected by increasing coccolithophorid bloom, which is associated with Atlantic water. Mn, Cu, Cd, and Ba significantly enrich the suspended particulate matter of the benthic nepheloid layer relative to the fluffy layer particulate matter within the benthic boundary layer