Mineralogy and chemistry of basalts and secondary minerals from DSDP Site 417, Atlantic Ocean

Basalts from DSDP Site 417 (109 Ma) exhibit the effects of several stages of alteration reflecting the evolution of seawater-derived solution compositions and control by the structure and permeability of the crust. Characteristic secondary mineral assemblages occur in often superimposed alteration zones within individual basalt fragments. By combining bulk rock and single phase chemical analyses with detailed mineralogic and petrographic studies, chemical changes have been determined for most of the alteration stages identified in the basalts. 1) Minor amounts of saponite, chlorite, and pyrite formed locally in coarse grained portions of massive units, possibly at high temperatures during initial cooling of the basalts. No chemical changes could be determined for this stage. 2) Possible mixing of cooled hydrothermal fluids with seawater resulted in the formation of celadonite-nontronite and Fe-hydroxide-rich black halos around cracks and pillow rims. Gains of K, Rb, H20, increase of Fe 3 +/FeT and possibly some losses of Ca and Mg occurred during this stage. 3a) Extensive circulation of oxygenated seawater resulted in the formation of various smectites, K-feldspar, and Fe-hydroxides in brown and light grey alteration zones around formerly exposed surfaces. K, Rb, H20, and occasionally P were added to the rocks, Fe3+/FeT increased, and Ca, Mg, Si and occasionally Al and Na were lost. 3 b) Anoxic alteration occurred during reaction of basalt with seawater at low water-rock ratios, or with seawater that had previously reacted with basalt. Saponite-rich dark grey alteration zones formed which exhibit very little chemical change: generally only slight increases in Fe 3 +/FeT and H20 occurred. 4) Zeolites and calcite formed from seawater-derived fluids modified by previous reactions with basalt. Chemical changes involved increases of Ca, Na, H20 , and CO2 in the rocks. 5) A late stage of anoxic conditions resulted in the formation of minor amounts of Mn-calcites and secondary sulfides in previously oxidized rocks. No chemical changes were determined for this stage. Recognition of such alteration sequences is important in understanding the evolution of submarine hydrothermal systems and in interpreting chemical exchange due to seawater-basalt reactions.

Compilation of Thunnus thynnus (bluefin tuna) catche in the Northeast Atlantic Ocean 1906-1949

The data have been extracted and compiled from various sources but mainly from the ICES data base. The ICES data are from catch databases downloaded from the ICES website on 2014-01-14. These data are resolved by ICES area, country and year. During inspection of these data, it was noted that Norwegian data for years before 1950 had not been entered into the catch database on the ICES website. ICES has been notified of this omission by B. R. MacKenzie. The Norwegian data from ICES Bulletins. Statistiques has been added. Additional historical bluefin tuna catch data from other fishery reports and sources have been included in the data file for years preceding those when countries started reported their landings officially to ICES. These additional data have been reported in the literature previously (MacKenzie and Myers 2007, Fisheries Research).

Concentration of atmospheric carbon dioxide on the Atlantic Ocean (Appendix)

During the 1965 Atlantic Expedition of the "Meteor" concentrations of various atmospheric trace gases were measured. The following gases were considered: carbon dioxide (CO2), sulfur dioxide (SO2), nitrogene dioxide (NO2), and nitric oxide (NO). The air whereof these components were measured was sucked in from a height of 14 m above the surface of the sea. The results allow conclusions upon the long term global increase of the atmospheric CO2 content, the meridional distribution of the CO2 on the Atlantic Ocean, and the dependance of its concentration upon the time of the day and the thermal structure of the atmosphere. Attempts at determining concentrations of sulfur dioxide and nitric oxide of non-continental origin failed at large. Concentrations of NO2, however, could succesfully be measured.