Chemiscal composition of basalts from DSDP Legs 69 and 70 Holes

Chemical compositions and 1-atm. phase relations were determined for basalts drilled from Holes 501, 504A, 504B, 505, and 505B on Legs 68, 69, and 70 of the Deep Sea Drilling Project. Chemical, experimental, and petrographic data indicate that these basalts are moderately evolved (Mg' values from 0.60 to 0.70), with olivine plus Plagioclase and often clinopyroxene on the liquidus. Chemical stratigraphy was used to infer that sequential influxes of magma into a differentiating magma chamber or separate flows from different magma chambers or both had occurred. Two major types of basalt were found to be inter layered: Group M, a rarely occurring type with major element chemistry and magmaphile element abundances within the range of the majority of ocean-floor basalts (TiO2 = 1.3%, Na2O 2.5%, Zr = 103 ppm, Nb = 2.5 ppm, and Y = 31 ppm); and Group D, a highly unusual series of basalt compositions that exhibit much lower magmaphile element abundances (TiO2 = 0.75-1.2%, Na2O = 1.7-2.3%, Zr = 34-60 ppm, Nb = 0.5-1.2 ppm, and Y = 16-27 ppm). The liquidus temperatures of the Group D basalts are high (1230- 1260°C) compared with those of other ocean-floor basalts of similar Mg' values. They have high CaO/Na2O ratios (5-8) and are calculated to be in equilibrium with unusually calcic Plagioclase (An78-84). The two basalt groups cannot be related by fractionation processes. However, constant Zr/Nb ratios (>40) for the two groups suggest a single mantle source, with differences in magmaphile element abundances and other element ratios (e.g., Zr/Ti, Zr/Y, Ce/Yb) arising through sequential melting of the same source. Magmas similar to Group D, if mixed with more typical mid-ocean-ridge basalt (MORB) magmas in shallow magma chambers, could provide a source for the highly calcic Plagioclase phenocrysts that appear in more common (i.e., less depleted) phyric ocean-floor basalts.

Chemical and physical oceanography on 131 CTD casts from METEOR cruise M59/2

The oceans absorb and store a significant portion of anthropogenic CO2 emissions, but large uncertainties remain in the quantification of this sink. An improved assessment of the present and future oceanic carbon sink is therefore necessary to provide recommendations for long-term global carbon cycle and climate policies. The formation of North Atlantic Deep Water (NADW) is a unique fast track for transporting anthropogenic CO2 into the ocean's interior, making the deep waters rich in anthropogenic carbon. Thus the Atlantic is presently estimated to hold 38% of the oceanic anthropogenic CO2 inventory, although its volume makes up only 25% of the world ocean. Here we analyze the inventory change of anthropogenic CO2 in the Atlantic between 1997 and 2003 and its relationship to NADW formation. For the whole region between 20°S and 65°N the inventory amounts to 32.5 ± 9.5 Petagram carbon (Pg C) in 1997 and increases up to 36.0 ± 10.5 Pg C in 2003. This result is quite similar to earlier studies. Moreover, the overall increase of anthropogenic carbon is in close agreement with the expected change due to rising atmospheric CO2 levels of 1.69% a?1. On the other hand, when considering the subpolar region only, the results demonstrate that the recent weakening in the formation of Labrador Sea Water, a component of NADW, has already led to a decrease of the anthropogenic carbon inventory in this water mass. As a consequence, the overall inventory for the total water column in the western subpolar North Atlantic increased only by 2% between 1997 and 2003, much less than the 11% that would be expected from the increase in atmospheric CO2 levels.

(Table 2) Geochemistry of K-feldspars and associated plagioclase phenocrysts and rims at DSDP Legs 69, 52, 51 and 19

Basalts from some holes of the Deep Sea Drilling Project contain secondary K-feldspar which forms pseudomorphs after calcic (>76% An) Plagioclase cores, whereas Plagioclase of rims and microlites (68-74% An) remains unaltered. In basalts of Hole 504B two such grains with relics of Plagioclase in the central parts of phenocysts were recovered. The composition of the Plagioclase rims and of non-replaced phenocrysts is An79-81; the composition of relics is An83. The An and Ab contents of the K-feldspar is higher than in K-feldspar from altered basalt in Hole 418A in the Atlantic Ocean near the Bermuda Rise. Replacement of plagioclases by K-feldspar evidently is caused by oxygen-rich nearbottom sea water penetrating into basalts. The temperature interval of K-feldspathization is probably in the range 30 to 80°C, more-calcic Plagioclase being replaced by K-feldspar at higher temperatures.

(Table 1) Sulfur isotopes, total sulfur, and degree of oxidation of basalt samples from DSDP Holes 69-504B and 70-504B

Whole-rock basalt samples from the upper half of Deep Sea Drilling Project Hole 504B have oxygen-isotope compositions typical of mid-ocean-ridge basalts which have experienced a moderate degree of low-temperature alteration by sea water. By contrast, d18O values in the lower half of the hole correspond to basalts which have experienced almost no detectable oxygen-isotope alteration. These observations suggest that the overall water/rock ratio was lower in the lower half of the drilled crust. A correlation between d18O values and 87Sr/86Sr ratios suggests that the water/rock ratio, rather than temperature variation, was the main factor determining basalt d18O values. Hydrogen-isotope data appear to be consistent with a low water/rock ratio in the lower part of the crust.