13 research outputs found

    A deep-sea coral record of North Atlantic radiocarbon through the Younger Dryas: Evidence for intermediate water/deepwater reorganization

    Get PDF
    Our record of Younger Dryas intermediate-depth seawater Δ^(14)C from North Atlantic deep-sea corals supports a link between abrupt climate change and intermediate ocean variability. Our data show that northern source intermediate water (∼1700 m) was partially replaced by (14)^C-depleted southern source water at the onset of the event, consistent with a reduction in the rate of North Atlantic Deep Water formation. This transition requires the existence of large, mobile gradients of Δ^(14)C in the ocean during the Younger Dryas. The Δ^(14)C water column profile from Keigwin (2004) provides direct evidence for the presence of one such gradient at the beginning of the Younger Dryas (∼12.9 ka), with a 100‰ offset between shallow (<∼2400 m) and deep water. Our early Younger Dryas data are consistent with this profile and also show a Δ^(14)C inversion, with 35‰ more enriched water at ∼2400 m than at ∼1700 m. This feature is probably the result of mixing between relatively well ^(14)C ventilated northern source water and more poorly ^(14)C ventilated southern source intermediate water, which is slightly shallower. Over the rest of the Younger Dryas our intermediate water/deepwater coral Δ^(14)C data gradually increase, while the atmosphere Δ^(14)C drops. For a very brief interval at ∼12.0 ka and at the end of the Younger Dryas (11.5 ka), intermediate water Δ^(14)C (∼1200 m) approached atmospheric Δ14C. These enriched Δ^(14)C results suggest an enhanced initial Δ^(14)C content of the water and demonstrate the presence of large lateral Δ^(14)C gradients in the intermediate/deep ocean in addition to the sharp vertical shift at ∼2500 m. The transient Δ^(14)C enrichment at ∼12.0 ka occurred in the middle of the Younger Dryas and demonstrates that there is at least one time when the intermediate/deep ocean underwent dramatic change but with much smaller effects in other paleoclimatic records

    Helium isotope ratios and sedimentation rate models of ODP holes

    No full text
    A continuous age model for the brief climate excursion at the Paleocene-Eocene boundary has been constructed by assuming a constant flux of extraterrestrial 3He (3He[ET]) to the seafloor. 3He[ET] measurements from ODP Site 690 provide quantitative evidence for the rapid onset (<few kyr) and short duration (<120 kyr) of global warming and of the associated disturbance to the Earth's surficial carbon budget at this time. These observations support astronomically calibrated age models indicating extremely rapid release of isotopically light carbon, possibly from seafloor methane hydrate, as the proximal cause of the event. However, the 3He[ET] technique indicates a previously unrecognized and extreme increase in sedimentation rate coincident with the return of climate proxies to pre-event values. The 3He[ET]-based age model thus suggests a far more rapid recovery from the climatic perturbation than previously proposed or predicted on the basis of the modern carbon cycle, and so may indicate additional or accelerated mechanisms of carbon removal from the ocean-atmosphere system during this period. 3He[ET] was also measured at ODP Site 1051 to test the validity of the Site 690 chronology. Comparison of these data sets seems to require removal of several tens of kyr of sediment within the climatic excursion at Site 1051, an observation consistent with sediment structures and previous age modeling efforts. The Site 1051 age model shows a ~30 kyr period in which climate proxies return toward pre-event values, after which they remain invariant for ~80 kyr. If this rise represents the recovery interval identified at Site 690, then the 3HeET-based age models of the two sites are in good agreement. However, alternative interpretations are possible, and work on less disrupted sites is required to evaluate the reliability of the proposed new chronology of the climate excursion. Regardless of these details, this work shows that the 3HeET technique can provide useful independent evidence for the development and testing of astronomically calibrated age models

    The transfer of bomb radiocarbon and anthropogenic lead to the deep North Atlantic Ocean observed from a deep sea coral

    No full text
    Deep-ocean, Δ^(14)C, Pb concentrations, and Pb isotopes were reconstructed from a deep-sea coral Enallopsammia rostrata from 1410 m depth off of Bermuda. Our high-resolution time series is created from closely spaced radial cross sections, with samples taken from the center of concentric coral growth bands that we show to be the oldest portion of the section. Prebomb radiocarbon ages from the coral demonstrate that the vertical growth rate of the coral is linear, and the age of the coral is estimated to be 560–630 yr old based on the growth rate. Using this age model to reconstruct Δ^(14)C in deep seawater, we first detect bomb radiocarbon at the coral growth site around 1980, and show that Δ^(14)C increased from −80±1‰−80±1‰ (average 1930–1979) to a plateau at −39±3‰ (1999–2001). Pb/Ca of the coral ranges between 1.1–4.5 nmol/mol during the 16th and 17th centuries, and Pb isotope ratios (^(206)Pb/^(207)Pb = 1.21, ^(208)Pb/^(207)Pb = 2.495) in this period agree with pre-anthropogenic values found in the pelagic sediments of the North Atlantic Ocean basin. Coral Pb/Ca is slightly elevated to 6.2±0.9 nmol/mol between the 1740s and the 1850s and then increases to 25.1±0.2 nmol/mol in the 1990s. The increase in coral Pb/Ca is accompanied by a decrease in coral ^(206)Pb/^(207)Pb and ^(208)Pb/^(207)Pb, indicating that the increase was caused by the infiltration of anthropogenic Pb to the coral growth site. Comparing our data to the surface coral Δ^(14)C and Pb records from Bermuda reveals a time scale of tracer transport from the surface ocean to the coral growth site. Some characteristic features, e.g., the bomb-derived Δ^(14)C increase, appear in the deep ocean approximately 25 yr later than the surface, but the overall increase of Δ^(14)C and Pb in the deep ocean is smaller and slower than the surface, showing the importance of mixing during the transport of these tracers

    A deep-sea coral record of the North Atlantic

    No full text
    Our record of Younger Dryas intermediate-depth seawater D14C from North Atlantic deep-sea corals supports a link between abrupt climate change and intermediate ocean variability. Our data show that northern source intermediate water (~1700 m) was partially replaced by 14C-depleted southern source water at the onset of the event, consistent with a reduction in the rate of North Atlantic Deep Water formation. This transition requires the existence of large, mobile gradients of D14C in the ocean during the Younger Dryas. The D14C water column profile from Keigwin (2004) provides direct evidence for the presence of one such gradient at the beginning of the Younger Dryas (~12.9 ka), with a 100 per mil offset between shallow (<~2400 m) and deep water. Our early Younger Dryas data are consistent with this profile and also show a D14C inversion, with 35 per mil more enriched water at ~2400 m than at ~1700 m. This feature is probably the result of mixing between relatively well 14C ventilated northern source water and more poorly 14C ventilated southern source intermediate water, which is slightly shallower. Over the rest of the Younger Dryas our intermediate water/deepwater coral D14C data gradually increase, while the atmosphere D14C drops. For a very brief interval at ~12.0 ka and at the end of the Younger Dryas (11.5 ka), intermediate water D14C (~1200 m) approached atmospheric D14C. These enriched D14C results suggest an enhanced initial D14C content of the water and demonstrate the presence of large lateral D14C gradients in the intermediate/deep ocean in addition to the sharp vertical shift at ~2500 m. The transient D14C enrichment at ~12.0 ka occurred in the middle of the Younger Dryas and demonstrates that there is at least one time when the intermediate/deep ocean underwent dramatic change but with much smaller effects in other paleoclimatic records

    The transfer of bomb radiocarbon and anthropogenic lead to the deep North Atlantic Ocean observed from a deep sea coral

    No full text
    Deep-ocean, Δ^(14)C, Pb concentrations, and Pb isotopes were reconstructed from a deep-sea coral Enallopsammia rostrata from 1410 m depth off of Bermuda. Our high-resolution time series is created from closely spaced radial cross sections, with samples taken from the center of concentric coral growth bands that we show to be the oldest portion of the section. Prebomb radiocarbon ages from the coral demonstrate that the vertical growth rate of the coral is linear, and the age of the coral is estimated to be 560–630 yr old based on the growth rate. Using this age model to reconstruct Δ^(14)C in deep seawater, we first detect bomb radiocarbon at the coral growth site around 1980, and show that Δ^(14)C increased from −80±1‰−80±1‰ (average 1930–1979) to a plateau at −39±3‰ (1999–2001). Pb/Ca of the coral ranges between 1.1–4.5 nmol/mol during the 16th and 17th centuries, and Pb isotope ratios (^(206)Pb/^(207)Pb = 1.21, ^(208)Pb/^(207)Pb = 2.495) in this period agree with pre-anthropogenic values found in the pelagic sediments of the North Atlantic Ocean basin. Coral Pb/Ca is slightly elevated to 6.2±0.9 nmol/mol between the 1740s and the 1850s and then increases to 25.1±0.2 nmol/mol in the 1990s. The increase in coral Pb/Ca is accompanied by a decrease in coral ^(206)Pb/^(207)Pb and ^(208)Pb/^(207)Pb, indicating that the increase was caused by the infiltration of anthropogenic Pb to the coral growth site. Comparing our data to the surface coral Δ^(14)C and Pb records from Bermuda reveals a time scale of tracer transport from the surface ocean to the coral growth site. Some characteristic features, e.g., the bomb-derived Δ^(14)C increase, appear in the deep ocean approximately 25 yr later than the surface, but the overall increase of Δ^(14)C and Pb in the deep ocean is smaller and slower than the surface, showing the importance of mixing during the transport of these tracers
    corecore