Halliday
Alex N.
Halliday
Alex N.
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PreprintSilicon isotopes in Antarctic sponges : an interlaboratory comparison( 2010-06-08) Hendry, Katharine R. ; Leng, Melanie J. ; Robinson, Laura F. ; Sloane, Hilary J. ; Blusztajn, Jerzy S. ; Rickaby, Rosalind E. M. ; Georg, R. Bastian ; Halliday, Alex N.Cycling of deep-water silicon (Si) within the Southern Ocean, and its transport into other ocean basins, may be an important player in the uptake of atmospheric carbon, and global climate. Recent work has shown that the Si isotope (denoted by δ29Si or δ30Si) composition of deep-sea sponges reflects the availability of dissolved Si during growth, and is a potential proxy for past deep and intermediate water silicic acid concentrations. As with any geochemical tool, it is essential to ensure analytical precision and accuracy, and consistency between methodologies and laboratories. Analytical bias may exist between laboratories, and sponge material may have matrix effects leading to offsets between samples and standards. Here, we report an interlaboratory evaluation of Si isotopes in Antarctic and subAntarctic sponges. We review independent methods for measuring Si isotopes in sponge spicules. Our results show that separate subsamples of non-homogenised sponges measured by three methods yield isotopic values within analytical error for over 80% of specimens. The relationship between δ29Si and δ30Si in sponges is consistent with kinetic fractionation during biomineralisation. Sponge Si isotope analyses show potential as palaeoceaongraphic archives, and we suggest Southern Ocean sponge material would form a useful additional reference standard for future spicule analyses.
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PreprintErratum to “Deep ocean nutrients during the Last Glacial Maximum deduced from sponge silicon isotopic compositions” [Earth Planet. Sci. Lett. 292 (2010) 290–300]( 2010-12) Hendry, Katharine R. ; Georg, R. Bastian ; Rickaby, Rosalind E. M. ; Robinson, Laura F. ; Halliday, Alex N.The relative importance of biological and physical processes within the Southern Ocean for the storage of carbon and atmospheric pCO2 on glacial-interglacial timescales remains uncertain. Understanding the impact of surface biological production on carbon export in the past relies on the reconstruction of the nutrient supply from upwelling deep-waters. In particular, the upwelling of silicic acid (Si(OH)4) is tightly coupled to carbon export in the Southern Ocean via diatom productivity. Here, we address how changes in deep-water Si(OH)4 concentrations can be reconstructed using the silicon isotopic composition of deep-sea sponges. We report δ30Si of modern deep-sea sponge spicules and show that they reflect seawater Si(OH)4 concentration. The fractionation factor of sponge δ30Si compared to seawater δ30Si shows a positive relationship with Si(OH)4, which may be a growth rate effect. Application of this proxy in two down-core records from the Scotia Sea reveals that Si(OH)4 concentrations in the deep Southern Ocean during the Last Glacial Maximum (LGM) were no different than today. Our result does not support a coupling of carbon and nutrient build up in an isolated deep-ocean reservoir during the LGM. Our data, combined with records of stable isotopes from diatoms, are only consistent with enhanced LGM Southern Ocean nutrient utilization if there was also a concurrent reduction in diatom silicification or a shift from siliceous to organic-walled phytoplankton.
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PreprintDeep ocean nutrients during the Last Glacial Maximum deduced from sponge silicon isotopic compositions( 2010-02) Hendry, Katharine R. ; Georg, R. Bastian ; Rickaby, Rosalind E. M. ; Robinson, Laura F. ; Halliday, Alex N.The relative importance of biological and physical processes within the Southern Ocean for the storage of carbon and atmospheric pCO2 on glacial-interglacial timescales remains uncertain. Understanding the impact of surface biological production on carbon export in the past relies on the reconstruction of the nutrient supply from upwelling deep-waters. In particular, the upwelling of silicic acid (Si(OH)4) is tightly coupled to carbon export in the Southern Ocean via diatom productivity. Here, we address how changes in deep-water Si(OH)4 concentrations can be reconstructed using the silicon isotopic composition of deep-sea sponges. We report δ30Si of modern deep-sea sponge spicules and show that they reflect seawater Si(OH)4 concentration. The fractionation factor of sponge δ30Si compared to seawater δ30Si shows a positive relationship with Si(OH)4, which may be a growth rate effect. Application of this proxy in two down-core records from the Scotia Sea reveals that Si(OH)4 concentrations in the deep Southern Ocean during the Last Glacial Maximum (LGM) were no different than today. Our result does not support a coupling of carbon and nutrient build up in an isolated deep-ocean reservoir during the LGM. Our data, combined with records of stable isotopes from diatoms, are only consistent with enhanced LGM Southern Ocean nutrient utilization if there was also a concur rent reduction in diatom silicification or a shift from siliceous to organic walled phytoplankton.
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PreprintRetreat of the Laurentide ice sheet tracked by the isotopic composition of Pb in western North Atlantic seawater during termination 1( 2009-07-16) Gutjahr, Marcus ; Frank, Martin ; Halliday, Alex N. ; Keigwin, Lloyd D.During the Last Glacial Maximum much of North America was covered by the Laurentide ice sheet. Its melting during termination 1 led to systematic changes in proglacial lake formation, continental runoff, and possibly North Atlantic Meridional Overturning Circulation. The accompanying change in chemical weathering rates in the interior of North America throughout the deglaciation resulted in a pronounced change in seawater Pb isotope composition in the western North Atlantic Ocean. Here we present the first high-resolution records of seawater Pb isotope variations of North Atlantic Deep Water extracted from authigenic Fe-Mn oxyhydroxides in three sediment cores (51GGC, 1790 m depth; 31GGC, 3410 m depth; 12JPC, 4250 m depth) from the Blake Ridge off Florida. These data reveal a striking excursion from relatively unradiogenic 206Pb/204Pb as low as 18.93 towards highly radiogenic Pb isotope compositions that was initiated during the Bølling-Allerød interstadial and was most pronounced in both intermediate and deep waters during and after the Younger Dryas (206Pb/204Pb as high as 19.38 at 8.8 ka in 4250 m). This pattern is interpreted to be a direct function of increased inflow of continent-derived radiogenic Pb into the western North Atlantic, supplied through chemical weathering of North American rocks that had been eroded and freshly exposed during the preceding glacial cycle. These sediment-derived data are complemented by new laser ablation Pb isotope data from a ferromanganese crust from the Blake Plateau at 850 m water depth, which show only small glacial-interglacial Pb isotope variations of the Florida Current (206Pb/204Pb between 19.07 and 19.16). The lack of change in the Blake Plateau record at the same time as the radiogenic excursion in the deeper sediments supports a northern origin of the pulse of radiogenic Pb. After the Younger Dryas, the deep western North Atlantic has experienced a persistent highly radiogenic Pb supply that was most pronounced during the first half of the Holocene and still lasts until today.
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PreprintTracing the Nd isotope evolution of North Atlantic Deep and Intermediate Waters in the western North Atlantic since the Last Glacial Maximum from Blake Ridge sediments( 2007-10-23) Gutjahr, Marcus ; Frank, Martin ; Stirling, Claudine H. ; Keigwin, Lloyd D. ; Halliday, Alex N.A high-resolution authigenic Nd isotope record has been extracted from the Fe-Mn oxyhydroxide fraction of drift sediments along the Blake Ridge in the North Atlantic. These sediments facilitate reconstruction of the timing and extent of major hydrographic changes in the western North Atlantic since the Last Glacial Maximum (LGM). This is one of the few locations where sediments were deposited in the major flow path of the Western Boundary Undercurrent (WBUC), which transports North Atlantic Deep Water (NADW) southward at the present day. The hydrodynamic setting, however, also causes problems. Authigenic Nd isotope compositions similar to the typical present-day NADW εNd value of –13.5 ± 0.5 were only extracted from sediments located within the main water body of the WBUC coinciding with the highest along slope current velocity below 3200 m water depth. Above this depth the authigenic Nd isotopic composition is more radiogenic than measured in a nearby seawater profile and appears to be influenced by downslope and lateral sediment redistribution. Our data suggest that these radiogenic signals were formed at shallow depths in Florida current waters, compromising the recorded ambient deep water Nd isotope signal in the Blake Ridge Fe-Mn oxyhydroxide coatings from intermediate depths during the Holocene and the deglaciation. The unradiogenic Nd isotopic composition typical of present-day NADW is not detectable along the Blake Ridge for any water depth during the LGM. Unlike the deglacial and Holocene sections, the intermediate core from 1790 m water depth did not experience significant sediment focussing during the LGM, in accord with the higher current velocities at this depth, suggesting that at this site an ambient LGM bottom water Nd isotope signal was recorded. Assuming this to be correct, our results indicate that the εNd of the shallower glacial equivalent of NADW, the Glacial North Atlantic Intermediate Water (GNAIW) may have been as radiogenic as –9.7 ± 0.4. Since the authigenic Nd isotope compositions of the Holocene and the deglacial sections of the intermediate depth sediment core were biased towards a shallow water signal, this first determination of a GNAIW εNd for the LGM will have to be corroborated by results from other locations and archives. The LGM and deglacial sediments below 3400 m water depth bear no evidence of an ambient deep water εNd as unradiogenic as -13.5. Although the deep core sites also experienced enhanced degrees of sediment focusing before the Younger Dryas, the εNd values of between -11 and – 10 are more readily explained in terms of increased presence of Southern Source Waters. If this is the case, the change to Nd isotopic compositions that reflect a modern circulation pattern, including the presence of Lower NADW, only occurred after the Younger Dryas.
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ArticleDiatom silicon isotopes as a proxy for silicic acid utilisation : a Southern Ocean core top calibration(Elsevier, 2012-08-11) Egan, Katherine E. ; Rickaby, Rosalind E. M. ; Leng, Melanie J. ; Hendry, Katharine R. ; Hermoso, Michael ; Sloane, Hilary J. ; Bostock, Helen ; Halliday, Alex N.Despite a growing body of work that uses diatom δ30Si to reconstruct past changes in silicic acid utilisation, few studies have focused on calibrating core top data with modern oceanographic conditions. In this study, a microfiltration technique is used to divide Southern Ocean core top silica into narrow size ranges, separating components such as radiolaria, sponge spicules and clay minerals from diatoms. Silicon isotope analysis of these components demonstrates that inclusion of small amounts of non-diatom material can significantly offset the measured from the true diatom δ30Si. Once the correct size fraction is selected (generally 2–20 μm), diatom δ30Si shows a strong negative correlation with surface water silicic acid concentration (R2 = 0.92), highly supportive of the qualitative use of diatom δ30Si as a proxy for silicic acid utilisation. The core top diatom δ30Si matches well with mixed layer filtered diatom δ30Si from published in situ studies, suggesting little to no effect of either dissolution on export through the water column, or early diagenesis, on diatom δ30Si in sediments from the Southern Ocean. However, the core top diatom δ30Si shows a poor fit to simple Rayleigh or steady state models of the Southern Ocean when a single source term is used. The data can instead be described by these models only when variations in the initial conditions of upwelled silicic acid concentration and δ30Si are taken into account, a caveat which may introduce some error into quantitative reconstructions of past silicic acid utilisation from diatom δ30Si.