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1 School of Civil Engineering and Geosciences, Newcastle University, Devonshire Building, Newcastle upon Tyne NE1 7RU, UK
2 Department of Earth and Atmospheric Sciences, 1-26 Earth Sciences Building, University of Alberta, Edmonton, Alberta T6G 2E3, Canada
3 Department of Marine Biogeochemistry and Toxicology, Royal Netherlands Institute for Sea Research, P.O. Box 59, 1790 AB Den Burg, Texel, Netherlands
4 Institute for Geology and Mineralogy, University of Cologne, Zülpicher Strasse 49a, 50674 Köln, Germany
| ABSTRACT |
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shift in leaf wax n-alkane 13C values at the onset of oceanic anoxic event (OAE) 1b from early Albian sediments off northwest Africa (Deep Sea Drilling Project Site 545) that is best explained by the rapid release of isotopically light carbon into the Cretaceous atmosphere. This -1.5
shift in the n-alkanes precedes a negative isotope excursion of similar magnitude observed in marine carbonate, organic matter, and algal steranes. A TEX86-based record of sea surface temperature (SST) confirms almost instantaneous warming by
3.5 °C along with the marine isotope shifts at Site 545, paralleled by an
2 °C TEX86-SST increase and a freshening of surface water salinity from 43 to 41 at Blake Nose, Ocean Drilling Program Site 1049. Multiproxy evidence indicates that, once established, these warm SSTs prevailed and were stable during OAE 1b, suggesting that the emission of 13C-depleted carbon started abruptly but then continued over tens of thousands of years. The SST cooled by
1–2 °C at the end of the event, not reaching pre-excursion levels. The new records provide evidence for a time lag (best estimate
1–3 k.y.) between atmospheric and oceanic processes that we interpret as a direct response to changes in the atmospheric greenhouse gas concentrations followed by propagation into the ocean and subsequent heating of surface waters.
Key Words: oceanic anoxic events sea surface temperature biomarkers atmosphere-ocean interactions biogeochemical cycling
| INTRODUCTION |
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To address the issue of climate perturbation and ocean response during Cretaceous OAEs we focus on the short (
45 k.y.) early Albian Paquier event (OAE 1b sensu stricto). The OAE 1b interval represents a major transition in Cretaceous tectonics, sea level, climate, lithofacies, and marine plankton communities, and also contains several prominent black shales (see Leckie et al., 2002, for review). OAE 1b is characterized by a distinct negative shift in various carbon reservoirs (Wagner et al., 2007) and high contributions of organic matter of non-thermophilic, marine archaeal origin in the subtropical and temperate ocean (Kuypers et al., 2001; Tsikos et al., 2004). Also documented is a distinct increase in sea-surface temperature (SST) and perturbations in the hydrological balance (Erbacher et al., 2001; Herrle et al., 2003). The causes and feedbacks of the OAE 1b carbon perturbation are still debated. Recent model simulations for Site 545 (Wagner et al., 2007) suggest an almost instantaneous average global warming of 0.3 °C at the onset of OAE 1b followed by
0.8 °C cooling for the remainder of the event, relative to pre-OAE levels. The match between simulations and stratigraphic data at Site 545 (Wagner et al., 2007) was interpreted to support earlier studies (Jenkyns, 2003) that proposed that enhanced methane emission triggered OAE 1b.
Here we report biomarker data from the Mazagan Plateau (Deep Sea Drilling Project, DSDP, Site 545) and Blake Nose Plateau (Ocean Drilling Program, ODP, Site 1049; Fig. 1) to provide constraints on the magnitude and timing of the isotopic excursion and on SSTs and surface water salinity (SSS) stability during OAE 1b.
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| METHODS |
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18O of calcite precipitated in equilibrium with seawater is determined by a combination of seawater temperature and
18O of water (
w), which can be related to salinity applying a global
w of –1.0
and mean salinity of seawater of 35.0
. To calculate SSS at Site 1049 we only used new TEX86-based SST and published
18O data (planktic foraminifera Hedbergella aff. H. trocoidea; Erbacher et al., 2001) from identical or very closely spaced samples intervals. | RESULTS |
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13 Ccarb) at Mazagan Plateau are
2
, rapidly decrease by
1.5
at the base of OAE 1b (390.7 mbsf), and remain at these relatively light values throughout most of the isotopic excursion before they reach postexcursion levels of
1.5
above 389.8 mbsf (Fig. 2; data from Wagner et al., 2007). Comparable
13 Ccarb records were reported from the west Atlantic and Tethyan OAE 1b sites (Fig. 1B). In the lower part of the Mazagan profile the 13C record of OC (
13 Corg) parallels that of
13 Ccarb (Fig. 2) containing 0.5
–1
variations in the pre-excursion and postexcursion, a negative shift of
1.5
at the base of the event (390.65–390.7 mbsf). Above 390.35 mbsf,
13 Corg follows a gradual return to less negative values up to –26
in the upper part of the event (390.0 mbsf), and a general decrease toward the top of excursion.
Concentrations in total OC (TOC) are
1.5% before OAE 1b (Fig. 2). The base of the event is marked by a 0.5% increase in TOC (at 390.56 mbsf) that proceeds in steps to almost 5% (at 389.9 mbsf) in the upper part of the isotopic excursion before it returns to the levels of the pre-excursion interval. The OC is immature (pyrolysis temperature, Tmax < 425 °C) and of type II kerogen (hydrogen indices
300 mg HC/g TOC with values exceeding 500 mg HC/g TOC in the black shale). Isotopically heavy archaeal-derived organic matter, characteristic for nonupwelling OAE 1b sites in the western Tethys and at Blake Nose (Kuypers et al., 2001; Tsikos et al., 2004), is not present at Site 545, probably owing to overall high nutrient level of surface waters off northwest Africa at that time (Leckie, 1984). This is also supported by the abundance of sterol ethers at Site 545 that have also been identified in sediments deposited below modern upwelling regions (Schouten et al., 2005). We consider that enhanced phytoplankton production off northwest Africa masked or out-competed the invasion of archaea during the early Albian evident from less productive sites.
Carbonate carbon content varies inversely to TOC, reaching average concentrations as low as 20% in the lower part of OAE 1b before it recovers to arrive at postexcursion levels (
40%–45%) exceeding those before the excursion (
38%; Fig. 2). In contrast to TOC, the carbonate trend is hardly interrupted at the critical interval marking the onset of the event (390.6–390.7 mbsf). Strong dissolution of calcareous nannofossils was not observed across the critical transition at the base of OAE 1b (390.6–390.7 mbsf).
Averaged
13C data from terrestrial plant leaf waxes (C 27, C29, C31 n-alkanes), with carbon preference indices ranging from 2.5 before and after the excursion to up to 7 within the TOC maximum, and marine algal C27-sterenes generally follow bulk
13Corg (Fig. 2); i.e., they are
–28.5
for n-alkanes and –31
for C27-sterenes before the OAE, then rapidly shift by 1
–2
to more negative values at the base of the OAE, and gradually return close to their pre-OAE values. Just below the base of the event (at 390.75 mbsf), the
13C values of n-alkanes start to decline to lighter values while
13C of sterenes do so
7 cm higher in the section (at 390.68 mbsf), concomitant with the onset of OAE 1b (Fig. 2). Both molecular records reveal slightly different trends throughout the event; i.e., the
13C values of the n-alkanes tend to follow
13 Ccarb except for the base of the OAE, whereas those of the C27-sterenes are similar to
13 Corg.
The TEX86-SST record at Site 545 (Fig. 2) reveals pre-excursion values of
29 °C, a rapid increase by
3.5 °C at the transition to the OAE (390.65–390 mbsf) concomitant with the negative shift in
13C of steranes and persistent high SSTs between 32 and 33 °C across the event, and a variable return to
30 °C following the isotopic excursion (from 389.9 mbsf). TEX86-SST data from OAE 1b at Site 1049 (Fig. 2) show a similar trend in SST for the lower part of the event (although the sampling resolution was lower), including an increase in SST of
2 °C (at 143.1 mbsf) before they dropped toward the end of OAE 1b.
| DISCUSSION |
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13C in various carbon reservoirs coincident with OAE 1b (Fig. 2). It has been proposed that the isotopic composition of terrestrial organic matter for the PETM is closely linked to the isotopic composition of atmospheric CO2 (Pagani et al., 2006) in the absence of major shifts in terrestrial vegetation (Schouten et al., 2007b). The sudden negative shift in 13C of n-alkanes at Site 545 is, therefore, probably best explained by a change in the 13C content of atmospheric CO2, although alternative mechanisms cannot be ruled out. The observation that the negative shift in the n-alkanes slightly precedes that of the marine records (Fig. 2) suggests that 13C-depleted carbon was abruptly released into the atmosphere and subsequently became mixed into surface waters.
The algal C27-sterene 13C record supports a sudden, though slightly delayed, response in oceanic surface waters relative to the atmosphere. Because the 13C values of n-alkanes remained at their depleted levels following the initial pulse, continuous emission of isotopically light carbon for
25–30 k.y. is invoked to maintain this signal for the duration of OAE 1b (Wagner et al., 2007). The divergence between constant
13 Ccarb and increasing
13 Corg and C27-sterene 13C values probably reflects the evolution of atmospheric pCO2, consistent with modeling results (Wagner et al., 2007). Model simulations of the negative
13C excursion quantified that a total of 1.3 x 1018 g methane carbon (
13C of –60
), or three times the amount of organic matter (
13C =–25
), must have been remineralized to generate the observed 13C excursion (Wagner et al., 2007). Simulation of emission as trigger for OAE volcanogenic CO2 1b did not provide realistic results consistent with the geological record and climate context; i.e., estimated volumes of greenhouse gas were unrealistically large (>300 Tmol. CO2 per yr). This emission would have led to an immediate acidification of the ocean, also leading to a positive rather than a negative isotopic excursion (K. Wallmann, 2007, personal commun.). Although the cause for the negative isotope excursion during OAE 1b remains a matter of discussion, we here focus on the impact of the global climate perturbation on SST and SSS.
Climatic Consequences of the Early Albian Emission of 13C-Depleted Carbon
Our observations at Site 545 suggest that SST responded to the injection of 13C-depleted carbon into the atmosphere with an offset represented by
7–10 cm (390.75–390.65 mbsf; Fig. 2). Assuming linear sedimentation rates of 1.2–2.4 cm/k.y. (Wagner et al., 2007) and continuous, noninterrupted sedimentation, that offset represents
1–3 k.y. The TEX86-SST data from Site 545 are consistent with the 32–34 °C warming at ODP Site 1049 (Fig. 2). The smaller amplitude in SST change off North America (
2 °C) in comparison to northwest Africa (
3–4 °C) may reflect prevailing upwelling of cooler waters off northwest Africa prior to the event. This mechanism probably temporarily slowed or even broke down as a consequence of OAE 1b, because upwelling processes probably did not occur off North America, explaining the generally warmer background SST. The Site 545 SST record indicates stable and extremely warm surface waters throughout most of OAE 1b, corroborating records from other OAEs that point toward long-term high SSTs (Wilson and Norris, 2001; Schouten et al., 2003), in some cases interrupted by short-term cooling events (Forster et al., 2007).
An initial increase in SST seems to be a characteristic feature not only for OAEs but also the PETM. For comparison, during the PETM, SST increased as much as 5 °C in the tropics and 8 °C in the high latitudes (Thomas et al., 2002; Zachos et al., 2006). Subtropical SST warming during the PETM was 2 °C or more higher than during OAE 1b, which is in agreement with a smaller input of 13C-depleted carbon into the atmosphere. Given the much larger global climate perturbation during the PETM, the SST increase during OAE 1b appears to be high, probably owing to strong regional amplification and positive feedback mechanisms on surface water warming (Wagner et al., 2007).
At Blake Nose, the TEX86-SST data can be compared with SST estimates derived from glassy planktic foraminiferal
18O (Erbacher et al., 2001). Recalculated
18O-based SST using a
w value of 0.52
(Peedee belemnite) based on corrections for latitude (Zachos et al., 1994) and temperature (Bemis et al., 1998) show as much as 4 °C warmer values compared to SST reported by Erbacher et al. (2001). These recalculated values, however, are still as much as 10 °C colder (19–24 °C) than the TEX86-SST data (32–34 °C; Fig. 3) and substantially lower than modern SST from the area (
27 °C; Levitus et al., 1998) suggesting a strong salinity effect on the
18O signal. The SSS calculated from TEX86 SST and
18O ranges from 41 to 43 for Blake Nose (Fig. 3), much higher than modern values of 35 (Levitus et al., 1998). A reduction in SSS from 43 to 41 at the onset of the OAE1b is observed, consistent with the proposed freshwater pulse from North America (Erbacher et al., 2001).
The TOC, SST, and SSS values dropped at the end of OAE 1b of the North Atlantic (Fig. 2), although not to pre-excursion levels. The reasons for the nonrecovery at the end of the excursion remain to be identified. As for carbon sequestration, we favor the interpretation that black shale deposition did not last long enough or was not widespread enough to fully compensate the global climate perturbation.
| CONCLUSION |
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1–3 k.y. This lead time may have been much shorter, but based on the resolution of the data presented, it cannot be determined more accurately at present. The Mazagan and Blake Nose records provide evidence for rapid warming of surface waters and subsequently the establishment of prolonged periods (
40–45 k.y.) of high SST. Although the causal relations, response times, and timing of atmosphere-ocean interactions must still remain somewhat speculative, this study provides new detailed geochemical evidence supporting rapid, widespread, and probably almost synchronous environmental change at both sides of the low-latitude early Albian North Atlantic.
| ACKNOWLEDGMENTS |
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| FOOTNOTES |
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Received for publication 19 February 2007
Revised manuscript received 30 October 2007
Manuscript accepted 30 October 2007
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| JOURNAL HOME | HELP | CONTACT PUBLISHER | SUBSCRIBE | ARCHIVE | SEARCH | TABLE OF CONTENTS |