Modelling phytoplankton succession on the Bering Sea shelf: role of climate influences and trophic interactions in generating Emiliania huxleyi blooms 1997-2000

Several years of continuous physical and biological anomalies have been affecting the Bering Sea shelf ecosystem starting from 1997. Such anomalies reached their peak in a striking visual phenomenon: the first appearance in the area of bright waters caused by massive blooms of the coccolithophore Emiliania huxleyi (E. huxleyi). This study is intended to provide an insight into the mechanisms of phytoplankton succession in the south-eastern part of the shelf during such years and addresses the causes of E. huxleyi success by means of a 2-layer ecosystem model, field data and satellite-derived information. A number of potential hypotheses are delineated based on observations conducted in the area and on previous knowledge of E. huxleyi general ecology. Some of these hypotheses are then considered as causative factors and explored with the model. The unusual climatic conditions of 1997 resulted most notably in a particularly shallow mixed layer depth and high sea surface temperature (about 4 °C above climatological mean). Despite the fact that the model could not reproduce for E. huxleyi a clear non-bloom to bloom transition (pre- vs. post-1997), several tests suggest that this species was favoured by the shallow mixed layer depth in conjunction with a lack of photoinhibition. A top-down control by microzooplankton selectively grazing phytoplankton other than E. huxleyi appears to be responsible for the long persistence of the blooms. Interestingly, observations reveal that the high N:P ratio hypothesis, regarded as crucial in the formation of blooms of this species in previous studies, does not hold on the Bering Sea shelf

Seasonal distribution of dissolved inorganic carbon and net community production on the Bering Sea shelf

Bering Sea, we measured the spatio-temporal distribution and controls on dissolved inorganic carbon (DIC) concentrations in spring and summer of 2008 across six shelf domains defined by differing biogeochemical characteristics. DIC concentrations were tightly coupled to salinity in spring and ranged from ~1900 ?moles kg?1 over the inner shelf to ~2400 ?moles kg?1 in the deeper waters of the Bering Sea. In summer, DIC concentrations were lower due to dilution from sea ice melt, terrestrial inputs, and primary production. Concentrations were found to be as low ~1800 ?moles kg?1 over the inner shelf. We found that DIC concentrations were drawn down 30–150 ?moles kg?1 in the upper 30 m of the water column due to primary production and calcium carbonate formation between the spring and summer occupations. Using the seasonal drawdown of DIC, estimated rates of NCP on the inner, middle, and outer shelf averaged 28 ± 9 mmoles C m?2 d?1. However, higher rates of NCP (40–47 mmoles C m?2 d?1) were observed in the "Green Belt" where the greatest confluence of nutrient-rich basin water and iron-rich shelf water occurs. We estimated that in 2008, total NCP across the shelf was on the order of ~96 Tg C yr?1. Due to the paucity of consistent, comparable productivity data, it is impossible at this time to quantify whether the system is becoming more or less productive. However, as changing climate continues to modify the character of the Bering Sea, we have shown that NCP can be an important indicator of how the ecosystem is functioning