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sediment cores from the tropical West Paci
c showing that the change in Mg/Ca
18 O foram signal by
measured in G. ruber leads its
δ
2,000 to
3,000 years
*
*
18 O foram and Mg/Ca values measured in foraminifera re
(Fig. 1 ). However,
ect
sea-surface temperature (SST) but both are also controlled by their dependency on
sea-surface salinity (SSS) which was quanti
δ
ed earlier by N
ü
rnberg et al. ( 1996 )
and con
rmed recently by Kisak
ü
rek et al. ( 2008 ). This implies that Mg/Ca re
ect a
18 O signal in planktonic foraminifera is inter-
preted by Visser et al. ( 2003 )tore
local/regional signal whereas the
δ
ect global rather than a local signal. Although
SSS variations may also interfere with the
18 O foram signal the Visser et al. ( 2003 )
hypothesis can be tested by a multi-proxy approach simultaneously using
δ
18 O foram ,
δ
44/40 Ca records applied to the same foraminiferal species of a sediment
core from the Caribbean. Thereby, Mg/Ca and
Mg/Ca and
δ
18 Oisre
δ
ecting differences in both
44/40 Ca is supposed to be solely temperature-driven,
independent from SSS variations (Gussone et al. 2004 ).
SST and SSS whereas
δ
44/40
Fig. 1 This figure shows the Mg/Ca (red G. sacc.; black G. ruber), δ
Ca (blue G. sacc.), and
18
δ
O records (green G. sacc.) values of two different foraminiferal species G. ruber and G.
sacculifer of core SO164-03-4 as a function of time (ka = 1,000 years); Y Younger Dryas,
A Aller ø d, B B ø lling. Mg/Ca and δ
44/40
Ca are in general accord after Termination I (red dotted line
at * 13 ka BP) but differ to a larger extend during the Glacial. There are clear indications for a
phase shift between Mg/Ca and δ
18
Oof * 4 ka between the Mg/Ca Termination and the lagging
18 O Termination (green dotted line at
behind
δ
9 ka BP) as it was reported earlier by Visser et al.
*
18 O values are roughly
( 2003 ). Note, that the
δ
2.5
too low when compared to the Mg/Ca
*
record in the critical age range between 13 and 9 ka BP
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