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Hubberten, Hans-Wolfgang (1983): (Table 1) Sulfur isotopes, total sulfur, and degree of oxidation of basalt samples from DSDP Hole 69-504B and 70-504B [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.816535, Supplement to: Hubberten, H-W (1983): Sulfur content and sulfur isotopes of basalts from the Costa Rica Rift (Hole 504B, Deep Sea Drilling Project Legs 69 and 70). In: Cann, JR; Langseth, MG; Honnorez, J; Von Herzen, RP; White, SM; et al. (eds.), Initial Reports of the Deep Sea Drilling Project (U.S. Govt. Printing Office), 69, 629-635, https://doi.org/10.2973/dsdp.proc.69.136.1983

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Abstract:
About 150 basalt samples from Hole 504B, near the Costa Rica Rift were analyzed for sulfur content and sulfur-isotope composition. The basement in Hole 504B can be divided into an upper part, which has oxidative alteration (274.5-550 m below sea floor), and a lower part, which has nonoxidative alteration (550-835 m below sea floor) (the interval from 540 to 585 meters actually is transitional). This division is reflected in both the sulfur content and the sulfurisotope composition. Oxidative alteration of basalts by sea water at low temperatures has resulted in a depletion in sulfur in the upper part of the hole (mostly less than 600 ppm S) as compared to fresh sulfur-saturated oceanic tholeiites (900-1200 ppm S). High amounts of sulfur in the lower part of the hole are a result of precipitation of secondary pyrite under non-oxidative or weakly oxidative conditions from solutions which dissolved igneous sulfides. The average sulfur-isotope composition of the primary igneous sulfides is d34S = -0.01 per mil, which is close to the assumed mantle sulfur composition (d34S = 0 per mil. Pyrite and sulfate sulfur extracted together in a separate preparation step (as "pyrite-sulfate" sulfur) indicate addition of sea-water sulfate to the upper part of the basalts. The d34S of secondary pyrite isolated by hand-picking varies between -8.0 and +5.8 per mil; the "pyrite-sulfate" sulfur (d34S = -4.8 to +10.5 per mil), as well as that of the isolated pyrite, may have originated in the precipitation of pyrite from solutions containing sulfur from the dissolution of igneous sulfides, but addition of sulfur transported by hydrothermal solutions cannot be excluded.
Project(s):
Coverage:
Median Latitude: 1.227100 * Median Longitude: -83.730100 * South-bound Latitude: 1.227000 * West-bound Longitude: -83.730200 * North-bound Latitude: 1.227200 * East-bound Longitude: -83.730000
Date/Time Start: 1979-10-07T00:00:00 * Date/Time End: 1979-12-04T00:00:00
Minimum Elevation: -3460.0 m * Maximum Elevation: -3460.0 m
Event(s):
69-504B * Latitude: 1.227200 * Longitude: -83.730200 * Date/Time: 1979-10-07T00:00:00 * Elevation: -3460.0 m * Penetration: 489 m * Recovery: 262 m * Campaign: Leg69 * Basis: Glomar Challenger * Method/Device: Drilling/drill rig (DRILL)
70-504B * Latitude: 1.227000 * Longitude: -83.730000 * Date/Time: 1979-12-04T00:00:00 * Elevation: -3460.0 m * Penetration: 836.1 m * Recovery: 91.6 m * Campaign: Leg70 * Basis: Glomar Challenger * Method/Device: Drilling/drill rig (DRILL) * Comment: 40 cores; 328.6 m cored; 18.5 m drilled; 27.9 % recovery
Parameter(s):
#NameShort NameUnitPrincipal InvestigatorMethod/DeviceComment
1Event labelEvent
2Sample code/labelSample labelHubberten, Hans-WolfgangDSDP/ODP/IODP sample designation
3Sample, optional label/labor noLab noHubberten, Hans-Wolfgang
4PiecePieceHubberten, Hans-Wolfgang
5δ34S, sulfideδ34S H2S‰ CDTHubberten, Hans-WolfgangMass spectrometry
6δ34S, pyriteδ34S Py‰ CDTHubberten, Hans-WolfgangMass spectrometry# = Separated anhydrite crystal
7δ34S, pyriteδ34S Py‰ CDTHubberten, Hans-WolfgangMass spectrometryPure pyrites separated under the binocular microscope
8Sulfur, totalTSmg/kgHubberten, Hans-Wolfgangsee reference(s)
9RatioRatioHubberten, Hans-WolfgangFe2O3/(FeO + Fe2O3) ratio
Size:
720 data points

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