Global climate evolution during the last deglaciation

Deciphering the evolution of global climate from the end of the Last Glacial Maximum approximately 19 ka to the early Holocene 11 ka presents an outstanding opportunity for understanding the transient response of Earth’s climate system to external and internal forcings. During this interval of global warming, the decay of ice sheets caused global mean sea level to rise by approximately 80 m; terrestrial and marine ecosystems experienced large disturbances and range shifts; perturbations to the carbon cycle resulted in a net release of the greenhouse gases CO_2 and CH_4 to the atmosphere; and changes in atmosphere and ocean circulation affected the global distribution and fluxes of water and heat. Here we summarize a major effort by the paleoclimate research community to characterize these changes through the development of well-dated, high-resolution records of the deep and intermediate ocean as well as surface climate. Our synthesis indicates that the superposition of two modes explains much of the variability in regional and global climate during the last deglaciation, with a strong association between the first mode and variations in greenhouse gases, and between the second mode and variations in the Atlantic meridional overturning circulation

Changing atmospheric Δ^(14)C and the record of deep water paleoventilation ages

We propose a new calculation method to better estimate the deep water ventilation age from benthic-planktonic foraminifera ^(14)C ages. Our study is motivated by the fact that changes in atmospheric Δ^(14)C through time can cause contemporary benthic and planktonic foraminifera to have different initial Δ^(14)C values. This effect can cause spurious ventilation age changes to be interpreted from the geologic data. Using a new calculation method, ^(14)C projection ages, we recalculate the data from the Pacific Ocean. Contrary to previous results, we find that the Pacific intermediate and deep waters were about 600 years older than today at the last glacial maximum. In addition, there are possible signals of ventilation age change prior to ice sheet melting and at the Younger Dryas. However, the data are still too sparse to constrain these ventilation transients

Compound-Specific δ^(34)S Analysis of Volatile Organics by Coupled GC/Multicollector-ICPMS

We have developed a highly sensitive and robust method for the analysis of δ^(34)S in individual organic compounds by coupled gas chromatography (GC) and multicollector inductively coupled plasma mass spectrometry (MC-ICPMS). The system requires minimal alteration of commercial hardware and is amenable to virtually all sample introduction methods. Isobaric interference from O_2^+ is minimized by employing dry plasma conditions and is cleanly resolved at all masses using medium resolution on the Thermo Neptune MC-ICPMS. Correction for mass bias is accomplished using standard−sample bracketing with peaks of SF6 reference gas. The precision of measured δ^(34)S values approaches 0.1‰ for analytes containing >40 pmol S and is better than 0.5‰ for those containing as little as 6 pmol S. This is within a factor of 2 of theoretical shot-noise limits. External accuracy is better than 0.3‰. Integrating only the center of chromatographic peaks, rather than the entire peak, offers significant gain in precision and chromatographic resolution with minimal effect on accuracy but requires further study for verification as a routine method. Coelution of organic compounds that do not contain S can cause degraded analytical precision. Analyses of crude oil samples show wide variability in δ^(34)S and demonstrate the robustness and precision of the method in complex environmental samples

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

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

Deep-sea corals : a new oceanic archive

Thesis (Ph. D.)--Massachusetts Institute of Technology, Dept. of Earth, Atmospheric, and Planetary Sciences, 1998.Vita.Includes bibliographical references.by Jess F. Adins.Ph.D

Synchronous volcanic eruptions and abrupt climate change ∼17.7 ka plausibly linked by stratospheric ozone depletion

Glacial-state greenhouse gas concentrations and Southern Hemisphere climate conditions persisted until ∼17.7 ka, when a nearly synchronous acceleration in deglaciation was recorded in paleoclimate proxies in large parts of the Southern Hemisphere, with many changes ascribed to a sudden poleward shift in the Southern Hemisphere westerlies and subsequent climate impacts. We used high-resolution chemical measurements in the West Antarctic Ice Sheet Divide, Byrd, and other ice cores to document a unique, ∼192-y series of halogen-rich volcanic eruptions exactly at the start of accelerated deglaciation, with tephra identifying the nearby Mount Takahe volcano as the source. Extensive fallout from these massive eruptions has been found >2,800 km from Mount Takahe. Sulfur isotope anomalies and marked decreases in ice core bromine consistent with increased surface UV radiation indicate that the eruptions led to stratospheric ozone depletion. Rather than a highly improbable coincidence, circulation and climate changes extending from the Antarctic Peninsula to the subtropics—similar to those associated with modern stratospheric ozone depletion over Antarctica—plausibly link the Mount Takahe eruptions to the onset of accelerated Southern Hemisphere deglaciation ∼17.7 ka

A Southern Ocean Mechanism for the Interhemispheric Coupling and Phasing of the Bipolar Seesaw

The last glacial period is punctuated by abrupt changes in Northern Hemisphere temperatures that are known as Dansgaard–Oeschger (DO) events. A striking and largely unexplained feature of DO events is an interhemispheric asymmetry characterized by cooling in Antarctica during periods of warming in Greenland and vice versa—the bipolar seesaw. Methane-synchronized ice core records indicate that the Southern Hemisphere lags the Northern Hemisphere by approximately 200 years. Here, we propose a mechanism that produces observed features of both the bipolar seesaw and the phasing of DO events. The spatial pattern of sea ice formation and melt in the Southern Ocean imposes a rigid constraint on where water masses are modified: waters are made denser near the coast where ice forms and waters are made lighter farther north where ice melts. This pattern, coupled to the tilt of density surfaces across the Southern Ocean and the stratification of the ocean basins, produces two modes of overturning corresponding to different bipolar seesaw states. We present evolution equations for a simplified ocean model that describes the transient adjustment of the basin stratification, the Southern Ocean surface density distribution, and the overturning strength as the ocean moves between these states in response to perturbations in North Atlantic Deep Water formation, which we take as a proxy for Greenland temperatures. Transitions between different overturning states occur over a multicentennial time scale, which is qualitatively consistent with the observed Southern Hemisphere lag. The volume of deep density layers varies inversely with the overturning strength, leading to significant changes in residence times. Evidence of these dynamics in more realistic circulation models is discussed

Carbonic anhydrase, coral calcification and a new model of stable isotope vital effects

The stable isotope compositions of biogenic carbonates have been used for paleoceanographic and paleoclimatic reconstructions for decades, and produced some of the most iconic records in the field. However, we still lack a fully mechanistic understanding of the stable isotope proxies, especially the biological overprint on the environmental signals termed “vital effects”. A ubiquitous feature of stable isotope vital effects in marine calcifying organisms is a strong correlation between δ^(18)O and δ^(13)C in a range of values that are depleted from inorganic calcite/aragonite. Two mechanisms have been proposed to explain this correlation, one based on kinetic isotope effects during CO_2(aq)-HCO_3− inter-conversion, the other based on equilibrium isotope exchange during pH dependent speciation of the dissolved inorganic carbon (DIC) pool. Neither mechanism explains all the stable isotope features observed in biogenic carbonates. Here we present a fully kinetic model of biomineralization and its isotope effects using deep-sea corals as a test organism. A key component of our model is the consideration of the enzyme carbonic anhydrase in catalyzing the CO2(aq)-HCO_3− inter-conversion reactions in the extracellular calcifying fluid (ECF). We find that the amount of carbonic anhydrase not only modulates the carbonate chemistry of the calcifying fluid, but also helps explain the slope of the δ^(18)O-δ^(13)C correlation. Differences in CA activity in the biomineralization process can possibly explain the observed range of δ^(18)O-δ^(13)C slopes in different calcifying organisms. A mechanistic understanding of stable isotope vital effects with numerical models can help us develop better paleoceanographic tracers

Seawater transport during coral biomineralization

Cation transport during skeletal growth is a key process controlling metal/calcium (Me/Ca) paleoproxy behavior in coral. To characterize this transport, cultured corals were transferred into seawater enriched in the rare earth element Tb^(3+) as well as stable isotopes of calcium, strontium, and barium. Subsequent NanoSIMS ion images of each coral skeleton were used to follow uptake dynamics. These images show a continuous region corresponding to new growth that is homogeneously enriched in each tracer. Isotope ratio profiles across the new growth boundary transition rapidly from natural abundance ratios to a ratio matching the enriched culture solution. The location of this transition is the same for each element, within analytical resolution. The synchronous incorporation of all these cations, including the dissimilar ion terbium, which has no known biological function in coral, suggests that: (1) there is cation exchange between seawater and the calcifying fluid, and (2) these elements are influenced by similar transport mechanisms consistent with direct and rapid seawater transport to the site of calcification. Measured using isotope ratio profiles, seawater transport rates differ from place to place on the growing coral skeleton, with calcifying fluid turnover times from 30 min to 5.7 h. Despite these differences, all the elements measured in this study show the same transport dynamics at each location. Using an analytical geochemical model of biomineralization that includes direct seawater transport we constrain the role of active calcium pumping during calcification and we show that the balance between seawater transport and precipitation can explain observed Me/Ca variability in deep-sea coral