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25th International Meeting on Organic Geochemistry IMOG 2011

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P-213<br />

Biomarker proxies indicate silicic acid transport from the<br />

Southern Ocean to southeastern Australia during interglacials<br />

Raquel Lopes dos Santos 1 , Daniel Wilkins 2 , Patrick De Deckker 2 , Stefan Schouten 1<br />

1 Royal Netherlands Institute for Sea Research (NIOZ), Texel, Netherlands, 2 The Australian Nati<strong>on</strong>al<br />

University (ANU), Canberra, Australia (corresp<strong>on</strong>ding author:raquel.santos@nioz.nl)<br />

The Southern Ocean (SO) has been<br />

identified as having a major role in regulating<br />

productivity at lower latitudes due to the formati<strong>on</strong> of<br />

different water masses that transport nutrients to<br />

other oceans. For instance, silicic acid is thought to<br />

be an important nutrient leaked from the SO during<br />

glacials via intermediate waters and stimulate<br />

phytoplankt<strong>on</strong> producti<strong>on</strong> at mid to lower latitudes.<br />

Additi<strong>on</strong>ally, plankt<strong>on</strong>ic foraminiferal carb<strong>on</strong> isotope<br />

minima during deglaciati<strong>on</strong>s have been observed in<br />

numerous cores from the southern hemisphere (SH)<br />

mid-lower latitudes and has been suggested as an<br />

isotopical signal of upwelled deep SO waters.<br />

Here we compared plankt<strong>on</strong>ic � 13 C of<br />

Globigerina bulloides with organic proxy records for<br />

Proboscia diatom (1,14-diol index) and haptophyte<br />

algae abundances (alken<strong>on</strong>es) from a core in the<br />

Murray Cany<strong>on</strong>s regi<strong>on</strong> of South East Australia (SEA)<br />

to estimate the influence of deep SO waters in the<br />

productivity of SEA. The Diol index is based <strong>on</strong> the<br />

rati<strong>on</strong> of 1,14 diols, lipids produced by Proboscia<br />

diatoms and 1,15 diols, lipids related to unidentified<br />

algae, possibly Eustigmatophytes. For haptophyte<br />

abundances, we measured alken<strong>on</strong>es distributi<strong>on</strong>,<br />

lipid specific for this group of algae.<br />

Our result shows that although SO waters<br />

were upwelled during deglaciati<strong>on</strong>s, as revealed by<br />

foraminifera isotopic minima, this did not result in<br />

increased productivity. Instead, Proboscia diatoms<br />

proliferated after the � 13 C minima during interglacials<br />

and MIS 3, likely because silicic acid was leaked to<br />

this area <strong>on</strong>ly after a SO decrease in diatom<br />

producti<strong>on</strong>. Furthermore, haptophyte algae <strong>on</strong>ly<br />

proliferated when Proboscia diatom productivity<br />

decreased suggesting that silicic acid c<strong>on</strong>centrati<strong>on</strong><br />

was insufficient for the needs of Proboscia.<br />

Thus, our study suggests a wider<br />

distributi<strong>on</strong> of silicic acid leakage during glacialinterglacial<br />

cycles likely c<strong>on</strong>trolled by the intensity of<br />

water masses transporting this nutrient.<br />

Fig. 1 Comparis<strong>on</strong> of geochemical records of core<br />

MD03-2607 from southeastern Australia with the opal<br />

flux record of a core in the SO. A) U K‘ 37 sea surface<br />

temperature, B) plankt<strong>on</strong>ic � 13 C of Globigerina<br />

bulloides, C) Diol index, D) alken<strong>on</strong>es c<strong>on</strong>centrati<strong>on</strong><br />

and E) Opal flux record from SO. Blue shaded area<br />

indicate periods of depleted plankt<strong>on</strong>ic � 13 C<br />

suggesting input of deep SO waters in the Murray<br />

Cany<strong>on</strong>s regi<strong>on</strong>.<br />

� 13 C G.bull.<br />

MD03-2607<br />

Alken<strong>on</strong>es 37:2+37:3<br />

[ng/g sed.]<br />

OPAL flux TN057-13<br />

[g cm -2 kyr -1 ]<br />

1.5<br />

1.0<br />

0.5<br />

0.0<br />

-0.5<br />

-1.0<br />

-1.5<br />

-2.0<br />

80<br />

60<br />

40<br />

20<br />

0<br />

7<br />

6<br />

5<br />

4<br />

3<br />

2<br />

1<br />

0<br />

0 10 20 30 40 50 60 70 80 90 100 110 120 130 140<br />

Age [kyrs]<br />

A<br />

B<br />

C<br />

D<br />

E<br />

22<br />

20<br />

18<br />

16<br />

14<br />

12<br />

10<br />

8<br />

0.6<br />

0.4<br />

0.2<br />

0.0<br />

2.0<br />

1.8<br />

1.6<br />

1.4<br />

1.2<br />

1.0<br />

0.8<br />

0.6<br />

Diol index<br />

MD03-2607<br />

OPAL flux TN057-14<br />

[g cm -2 kyr -1 ]<br />

352<br />

U K'<br />

37 SST<br />

[ 0 C]

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