Faul, Kristina L.; Paytan, Adina (2006): Phosphorus and barite concentrations and geochemistry in Site 1221 Paleocene/Eocene boundary sediments. Texas A&M University, Ocean Drilling Program, College Station, TX, United States, In: Wilson, Paul A., Lyle, Mitchell W., Janecek, Thomas R., Backman, Jan, Busch, William H., Coxall, Helen K., Faul, Kristina, Gaillot, Philippe, Hovan, Steven A., Knoop, Peter, Kruse, Silke, Lanci, Luca, Lear, Caroline, Moore, Theodore C., Nigrini, Catherine A., Nishi, Hiroshi, Nomura, Ritsuo, Norris, Richard D., Palike, Heiko, Pares, Josep M., Quintin, Lacie, Raffi, Isabella, Rea, Brice R., Steiger, Torsten H., Tripati, Aradhna, Vanden Berg, Michael D., Wade, Bridget, Proceedings of the Ocean Drilling Program; scientific results; Paleogene equatorial transect; covering Leg 199 of the cruises of the drilling vessel JOIDES Resolution; Honolulu, Hawaii, to Honolulu, Hawaii; Sites 1215-1222; 23 October-16 December 2001, 199, georefid:2007-028678

Abstract:
We determined changes in equatorial Pacific phosphorus (mu mol P/g) and barite (BaSO (sub 4) ; wt%) concentrations at high resolution (2 cm) across the Paleocene/Eocene (P/E) boundary in sediments from Ocean Drilling Program (ODP) Leg 199 Site 1221 (153.40 to 154.80 meters below seafloor [mbsf]). Oxide-associated, authigenic, and organic P sequentially extracted from bulk sediment were used to distinguish reactive P from detrital P. We separated barite from bulk sediment and compared its morphology with that of modern unaltered biogenic barite to check for diagenesis. On a CaCO (sub 3) -free basis, reactive P concentrations are relatively constant and high (323 mu mol P/g or approximately 1 wt%). Barite concentrations range from 0.05 to 5.6 wt%, calculated on a CaCO (sub 3) -free basis, and show significant variability over this time interval. Shipboard measurements of P and Ba in bulk sediments are systematically lower (by approximately 25%) than shore-based concentrations and likely indicate problems with shipboard standard calibrations. The presence of Mn oxides and the size, crystal morphology, and sulfur isotopes of barite imply deposition in sulfate-rich pore fluids. Relatively constant reactive P, organic C, and biogenic silica concentrations calculated on a CaCO (sub 3) -free basis indicate generally little variation in organic C, reactive P, and biogenic opal burial across the P/E boundary, whereas variable barite concentrations indicate significant changes in export productivity. Low barite Ba/reactive P ratios before and immediately after the Benthic Extinction Event (BEE) may indicate efficient nutrient burial, and, if nutrient burial and organic C burial are linked, high relative organic C burial that could temporarily drawdown CO (sub 2) at this site. This interpretation requires postdepositional oxidation of organic C because organic C to reactive P ratios are low throughout the section. After the BEE, higher barite Ba/reactive P ratios combined with higher barite Ba concentrations may imply that higher export productivity was coupled with unchanged reactive P burial, indicating efficient nutrient and possibly also organic C recycling in the water column. If the nutrient recycling is decoupled from organic C, the high export production could be indicative of drawdown of CO (sub 2) . However, the observation that organic C burial is not high where barite burial is high may imply that either C sequestration was restricted to the deep ocean and thus occurred only on timescales of the deep ocean mixing or that postdepositional oxidation (burn down) of organic matter affected the sediments. The decoupling of barite and opal may result from low opal preservation or production that is not diatom based.
Coverage:
West: -143.4200 East: -143.4200 North: 12.0200 South: 12.0200
Relations:
Expedition: 199
Site: 199-1221
Supplemental Information:
Available only on CD-ROM in PDF format and on the Web in PDF or HTML
Data access:
Provider: SEDIS Publication Catalogue
Data set link: http://sedis.iodp.org/pub-catalogue/index.php?id=10.2973/odp.proc.sr.199.214.2006 (c.f. for more detailed metadata)
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