Seawater carbonate chemistry, gross photosynthesis and metabolically induced rate of pH change during experiments with macroalgae, 2012

Ocean acidification (OA) is a reduction in oceanic pH due to increased absorption of anthropogenically produced CO2. This change alters the seawater concentrations of inorganic carbon species that are utilized by macroalgae for photosynthesis and calcification: CO2 and HCO3 increase; CO32 decreases. Two common methods of experimentally reducing seawater pH differentially alter other aspects of carbonate chemistry: the addition of CO2 gas mimics changes predicted due to OA, while the addition of HCl results in a comparatively lower [HCO3]. We measured the short-term photosynthetic responses of five macroalgal species with various carbon-use strategies in one of three seawater pH treatments: pH 7.5 lowered by bubbling CO2 gas, pH 7.5 lowered by HCl, and ambient pH 7.9. There was no difference in photosynthetic rates between the CO2, HCl, or pH 7.9 treatments for any of the species examined. However, the ability of macroalgae to raise the pH of the surrounding seawater through carbon uptake was greatest in the pH 7.5 treatments. Modeling of pH change due to carbon assimilation indicated that macroalgal species that could utilize HCO3 increased their use of CO2 in the pH 7.5 treatments compared to pH 7.9 treatments. Species only capable of using CO2 did so exclusively in all treatments. Although CO2 is not likely to be limiting for photosynthesis for the macroalgal species examined, the diffusive uptake of CO2 is less energetically expensive than active HCO3 uptake, and so HCO3-using macroalgae may benefit in future seawater with elevated CO2.

Millenial-Scale stable oxygen isotope record of ODP Site 172-1058

We use the oxygen isotopic composition of planktonic foraminifera Globigerinoides ruber (white) from Ocean Drilling Program Site 1058 in the subtropical northwestern Atlantic to construct a high-resolution (~800 year) climate record spanning the mid-Pleistocene climate transition (~410 ka to 1350 ka). We investigate whether or not millennial-scale instabilities in the proxy record are associated with the extent of continental glaciation. G. ruber d18O values display high-frequency fluctuations throughout the record, but the amplitude about mean glacial and interglacial d18O values increases at marine isotope stage (MIS) 22 (880 ka) and is highest during MIS 12. These observations support that millennial-scale climate instabilities are associated with ice sheet size. Time series analysis illustrates that these variations have significant concentration of spectral power centered on periods of ~10-12 ka and ~5 ka. The timing of these fluctuations agrees well, or coincides with, the periodicities of the second and fourth harmonics, respectively, of precessional forcing at the equator. An insolation-based origin of the millennial-scale instabilities would be independent of ice volume and explains the presence of these fluctuations before the mid-Pleistocene climate transition as well as during interglacial intervals (e.g., MIS 37 and 17). Because the amplitude of the millennial-scale variations increases during the mid-Pleistocene transition, feedback mechanisms associated with the growth of large, 100-ka-paced, polar ice sheets may be important amplifiers of regional surface water hydrographic changes.

Den Norske Nordhavs-expedition, 1876-1878.

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