Coupled changes in western South Atlantic carbon sequestration and particle reactive element cycling during millennial-scale Holocene climate variability

AbstractContinental shelves have the potential to remove atmospheric carbon dioxide via the biological pump, burying it in seafloor sediments. The efficiency of marine carbon sequestration changes rapidly due to variations in biological productivity, organic carbon oxidation, and burial rate. Here we present a high temporal resolution record of marine carbon sequestration changes from a western South Atlantic shelf site sensitive to Brazil Current-driven upwelling. The comparison of biological records to rare earth element (REE) patterns from authigenic oxides shows a strong relationship between higher biological productivity and stronger particle reactive element cycling (i.e. REE cycling) during rapid climate change events. This is the first evidence that authigenic oxides archive past changes in upper ocean REE cycling by the exported organic carbon. In addition, our data suggest that Brazil Current-driven upwelling varies on millennial-scales and in time with continental precipitation anomalies as registered in Brazilian speleothems during the Holocene. This indicates an ocean–atmosphere control on the biological pump, most probably related to South American monsoon system variability.

Origins of a Low-Sulfur Superalloy Al2O3 Scale Adhesion Map

Low-sulfur single-crystal Ni-base superalloys have demonstrated excellent cyclic oxidation resistance due to improved Al2O3 scale adhesion. This derives from preventing deleterious interfacial sulfur segregation that occurs at common ppm levels of S impurity. Multiple hydrogen-annealing desulfurization treatments were employed to produce a continuum of levels demonstrating this oxidative transition, using 1 h cyclic oxidation at 1100 °C for 500 h to 1000 h. The sulfur content was determined by glow discharge mass spectrometry. The complete gravimetric database of 25 samples is revealed and correlated with sulfur content. Maximum adhesion (i.e., no weight loss) was achieved at ≤ 0.3 ppmw S, significant spallation (20–30 mg/cm2) above 2 ppmw, with transitional behavior between 0.3 and 2 ppmw S. A map suggested that adhesion was enabled when the total sulfur reservoir was less than one S atom per Ni interface atom. Equilibrium models further suggest that segregation may be minimized (~1% at 0.2 ppmw bulk), regardless of section thickness. 1st order adhesion effects have thus been demonstrated for PWA 1480 having no Y, Zr, or Hf reactive element dopants and no possibility of confounding reactive element effects. The results are compared with 2nd generation PWA 1484, Rene’N5, N6, and CMSX-4® SLS, all having Hf dopants.

Potential Application of Ionic Liquids for Electrodeposition of the Material Targets for Production of Diagnostic Radioisotopes

An overview of the reported electrochemistry studies on the chemistry of the element for targets for isotope production in ionic liquids (ILs) is provided. The majority of investigations have been dedicated to two aspects of the reactive element chemistry. The first part of this review presents description of the cyclotron targets properties, especially physicochemical characterization of irradiated elements. The second part is devoted to description of the electrodeposition procedures leading to obtain elements or their alloys coatings (e.g., nickel, uranium) as the targets for cyclotron and reactor generation of the radioisotopes. This review provides an evaluation of the role ILs can have in the production of isotopes.