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What is the temporal variability of the elemental stoichiometry of marine microbial communities across ocean regions? To answer this question, we present an analysis of environmental conditions, particulate organic carbon, nitrogen, and phosphorus concentrations and their ratios across 20 time series (3–25 years duration) representing estuarine, coastal, and open ocean environments. The majority of stations showed significant seasonal oscillations in particulate organic elemental concentrations and ratios. However, shorter-term changes contributed most to overall variance in particulate organic matter concentrations and ratios. We found a correlation between the seasonal oscillations of environmental conditions and elemental ratios at many coastal but not open ocean and estuarine stations. C:N peaked near the seasonal temperature minimum and nutrient maximum, but some stations showed other seasonal links. C:N ratios declined with time over the respective observation periods at all open ocean and estuarine stations as well as at five coastal station but increased at the nine other coastal stations. C:P (but not N:P) declined slightly at Bermuda Atlantic Time-series Study but showed large significant increases at Hawaii Ocean Time-series and Arendal stations. The relationships between long-term changes in environmental conditions and particulate organic matter concentrations or ratios were ambiguous, but interactions between changes in temperature and nutrient availability were important. Overall, our analysis demonstrates significant changes in elemental ratios at long-term and seasonal time scales across regions, but the underlying mechanisms are currently unclear. Thus, we need to better understand the detailed mechanisms driving the elemental composition of marine microbial ecosystems in order to predict how oceans will respond to environmental changes.

[1] Surface δ15NPON increased 3.92 ± 0.48‰ over the course of 20 days following additions of iron (Fe) to an eddy in close proximity to the Antarctic Polar Front in the Atlantic sector of the Southern Ocean. The change in δ15NPON was associated with an increase in the >20 μm size fraction, leading to a maximal difference of 6.23‰ between the >20 μm and

[1] The impact of iron fertilization on mesopelagic carbon (C) remineralization was assessed during the European Iron Fertilization Experiment (EIFEX) in the Southern Ocean by following the temporal change of excess particulate barium (also called biogenic or Baxs) in the mesopelagic waters of a mesoscale eddy. Before the iron infusion the site was already sustaining a significant vertical flux of particles leading to organic remineralization in the mesopelagic. Approximately 35 d after the fertilization, mesopelagic Baxs contents provided evidence of changes in surface particulate export and of enhanced and particularly fast remineralization extending down to 1000 m. At the end of the experiment (day 36) both export and remineralization decreased. Organic carbon remineralization took place mainly in the lower part of the mesopelagic zone (500–1000 m) and increased more than 5-fold during EIFEX, reaching values up to 92 ± 15 mg C m−2 d−1. However, such remineralization rates are not particularly high when compared to other values reported for the natural Southern Ocean during summer. Though export and remineralization reached peak values around day 34, remineralization integrated over the 150 to 1000 m layer accounted only for 13 ± 1.4% of the export at 150 m, suggesting that a substantial amount of exported carbon reached deeper in the water column. Compared to natural blooms in high-nutrient low-chlorophyll (HNLC) waters of the Southern Ocean, the Fe-induced bloom during EIFEX resulted in a lower ratio of remineralized organic carbon over exported carbon, similar to what we recently observed for natural Fe-replete conditions prevailing above the Kerguelen Plateau. Unexpected similarities and phase lags of profiles in the mesopelagic between casts sampled inside and outside the fertilized patch during EIFEX indicated that eddy dynamics were a determinant in setting particle patterns on a broad spatial scale exceeding the extent of the fertilization, thereby homogenizing the signals of mesopelagic remineralization.

[1] We analyzed δ29Si of dissolved silicate for eight water column profiles across the Southern Ocean (south of Australia in spring 2001) from the Seasonal Ice Zone (SIZ) north to the Subantarctic Zone (SAZ), including the first isotopic compositions measured for Si-depleted seawaters. All profiles display mixed layer enrichments in heavy Si isotopes relative to deep water in accordance with preferential uptake of the light isotope by diatoms. As silicate levels decrease from the SIZ northward across the Polar Front Zone (PFZ) to the SAZ, surface and mesopelagic δ29Si signatures generally become progressively heavier, but the most Si-depleted SAZ waters do not exhibit δ29Si values heavier than in the PFZ. This intricacy appears to derive from variations in the vertical and horizontal supply of silicate to surface waters, and by applying a steady state open system model, we estimate a fractionation factor, 29ɛ, between diatoms and seawater of −0.45 ± 0.17‰, independently of zones and phytoplankton community. Though encouraging, these results are related to latitudinal changes in mesopelagic δ29Si values, complexity in surface silicate−δ29Si correlations, and differences from previous studies, which underline the need for caution in the use of silicon isotopes in paleoceanographic studies until systematic efforts have been undertaken to better understand modern variations.