Other
Scientific paper
Sep 1991
adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=1991gecoa..55.2453m&link_type=abstract
Geochimica et Cosmochimica Acta, vol. 55, Issue 9, pp.2453-2466
Other
4
Scientific paper
The relative effects of paleoceanographic and paleogeographic variations, sediment lithology, and diagenetic processes on the recorded rare earth element (REE) chemistry of Japan Sea sediments are evaluated by investigating REE total abundances and relative fractionations in 59 samples from Ocean Drilling Program Leg 127. REE total abundances ( REE) in the Japan Sea are strongly dependent upon the paleoceanographic position of a given site with respect to terrigenous and biogenic sources. REE concentrations at Site 794 (Yamato Basin) overall correspond well to aluminosilicate chemical indices and are strongly diluted by SiO 2 within the late Miocene-Pliocene diatomaceous sequence. Eu / Eu * values at Site 794 reach a maximum through the diatomaceous interval as well, most likely suggesting an association of Eu / Eu * with the siliceous component, or reflecting slight incorporation of a detrital feldspar phase. REE at Site 795 (Japan Basin) also is affiliated strongly with aluminosilicate phases, yet is diluted only slightly by siliceous input. At Site 797 (Yamato Basin), REE is not as clearly associated with the aluminosilicate fraction, is correlated moderately to siliceous input, and may be sporadically influenced by detrital heavy minerals originating from the nearby rifted continental fragment composing the Yamato Rise. The biogenic influence is largest at Site 794, moderately developed at Site 797, and of only minor importance at Site 795, reflecting basinal contrasts in productivity such that the Yamato Basin records greater biogenic input than the Japan Basin, while the most productive waters overlie the easternmost sequence of Site 794. Ce / Ce * profiles at all three sites increase monotonically with depth, and record progressive diagenetic LREE fractionation. The observed Ce / Ce * record does not respond to changes in oxygenation state of the overlying water, and Ce / Ce * correlates slightly better with depth than with age. The downhole increase in Ce / Ce * at Site 794 and Site 797 is a passive response to diagenetic transfer of LREE (except Ce) from sediment to interstitial water. At Site 795, the overall lack of correlation between Ce / Ce * and La n / Yb n suggests that other processes are occurring which mask the diagenetic behavior of all LREEs. First-order calculations of the Ce budget in Japan Sea waters and sediment indicate that ~20% of the excess Ce adsorbed by settling particles is recycled within the water column, and that an additional ~38% is recycled at or near the seafloor (data from and , 1989). Thus, because the remaining excess Ce is only ~10% of the total Ce, there is not a large source of Ce to the deeply buried sediment, further suggesting that the downhole increase in Ce / Ce * is a passive response to diagenetic behavior of the other LREEs. The REE chemistry of Japan Sea sediment therefore predicts successive downhole addition of LREEs to deeply-buried interstitial waters.
Brumsack Hans-Jürgen
Buchholtzten Brink Marilyn R.
Gerlach David C.
Murray Richard W.
Price Russ III G.
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