Kirsty C. Crocket
Scottish Association for Marine Science
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Featured researches published by Kirsty C. Crocket.
Geology | 2011
Kirsty C. Crocket; Derek Vance; Marcus Gutjahr; Gavin L. Foster; David A. Richards
North Atlantic climate is very sensitive to overturning in the Greenland-Iceland-Norwegian (GIN) Seas, overflow of deep water into the North Atlantic via the Greenland-Iceland-Scotland Ridge, and compensating northward flow of warm surface water. Physical models suggest that, in the absence of such overturning, oceanic heat transport to the Northern Hemisphere is reduced by as much as 50%, open North Atlantic sea-surface temperatures are as much as 6 °C lower, and the winter sea-ice limit migrates as far south as 45°N. Although simulations of the equilibrium climate state for the Last Glacial Maximum (LGM) suggest the absence of GIN Seas overflow, tests of these model results have been hampered by ambiguity in sedimentary proxies. Here we present a bottom-water neodymium (Nd) isotope record from the Rockall Trough to investigate changes in the sources of circulating waters over the past 43 k.y. Today and throughout most of the Holocene, water from the GIN Seas, along with water from the North Atlantic Current (NAC) entrained during overflow, sets the bottom-water Nd isotope composition of the Rockall Trough to ∼–10. Our results suggest the persistence of this scenario back into the LGM and beyond to mid-Marine Isotope Stage 3. Periodic radiogenic excursions punctuate the record at times of meltwater events, implying either continued GIN Seas overflow without NAC entrainment, or millennial-scale interruptions in the overflow and shoaling of Southern Source Water. We conclude that overflow was at least intermittently present during the LGM, if not continuous, and that the GIN Seas have remained a source of deep water to the North Atlantic during the last glacial cycle.
Paleoceanography | 2014
David J. Wilson; Kirsty C. Crocket; Tina van de Flierdt; Laura F. Robinson; Jess F. Adkins
The last deglaciation was characterised by a series of millennial scale climate events that have been linked to deep ocean variability. While often implied in interpretations, few direct constraints exist on circulation changes at mid-depths. Here we provide new constraints on the variability of deglacial mid-depth circulation using combined radiocarbon and neodymium isotopes in 24 North Atlantic deep-sea corals. Their aragonite skeletons have been dated by uranium-series, providing absolute ages and the resolution to record centennial scale changes, while transects spanning the lifetime of a single coral allow sub-centennial tracer reconstruction. Our results reveal that rapid fluctuations of water mass sourcing and radiocarbon affected the mid-depth water column (1.7-2.5 km) on timescales of less than 100 years during the latter half of Heinrich Stadial 1. The neodymium isotopic variability (−14.5 to −11.0) ranges from the composition of the modern northern-sourced waters towards more radiogenic compositions that suggest the presence of a greater southern-sourced component at some times. However, in detail, simple two-component mixing between well-ventilated northern-sourced and radiocarbon-depleted southern-sourced water masses cannot explain all our data. Instead, corals from ~15.0 ka and ~15.8 ka may record variability between southern-sourced intermediate waters and radiocarbon-depleted northern-sourced waters, unless there was a major shift in the neodymium isotopic composition of the northern endmember. In order to explain the rapid shift towards the most depleted radiocarbon values at ~15.4 ka, we suggest a different mixing scenario involving either radiocarbon-depleted deep water from the Greenland-Iceland-Norwegian Seas or a southern-sourced deep water mass. Since these mid-depth changes preceded the Bolling-Allerod warming, and were apparently unaccompanied by changes in the deep Atlantic, they may indicate an important role for the intermediate ocean in the early deglacial climate evolution.
Geochemistry Geophysics Geosystems | 2016
Torben Struve; Tina van de Flierdt; Laura F. Robinson; Louisa I. Bradtmiller; Sophia K. Hines; Jess F. Adkins; Myriam Lambelet; Kirsty C. Crocket; Katharina Kreissig; Barry J. Coles; Maureen E. Auro
Isotopes of the actinide elements protactinium (Pa), thorium (Th), and uranium (U), and the lanthanide element neodymium (Nd) are often used as complementary tracers of modern and past oceanic processes. The extraction of such elements from low abundance matrices, such as seawater and carbonate, is however labor-intensive and requires significant amounts of sample material. We here present a combined method for the extraction of Pa, Th, and Nd from 5 to 10 L seawater samples, and of U, Th, and Nd from <1 g carbonate samples. Neodymium is collected in the respective wash fractions of Pa-Th and U-Th anion exchange chromatographies. Regardless of the original sample matrix, Nd is extracted during a two-stage ion chromatography, followed by thermal ionization mass spectrometry (TIMS) analysis as NdO+. Using this combined procedure, we obtained results for Nd isotopic compositions on two GEOTRACES consensus samples from Bermuda Atlantic Time Series (BATS), which are within error identical to results for separately sampled and processed dedicated Nd samples (e_(Nd) = −9.20 ± 0.21 and −13.11 ± 0.21 for 15 and 2000 m water depths, respectively; intercalibration results from 14 laboratories: e_(Nd) = −9.19 ± 0.57 and −13.14 ± 0.57). Furthermore, Nd isotope results for an in-house coral reference material are identical within analytical uncertainty for dedicated Nd chemistry and after collection of Nd from U-Th anion exchange chromatography. Our procedure does not require major adaptations to independently used ion exchange chromatographies for U-Pa-Th and Nd, and can hence be readily implemented for a wide range of applications.
Frontiers in Marine Science | 2018
Kirsty C. Crocket; Emily Hill; Richard Abell; Clare Johnson; Stefan F. Gary; Tim Brand; Ed C. Hathorne
Seawater rare earth element (REE) concentrations are increasingly applied to reconstruct water mass histories by exploiting relative changes in the distinctive normalised patterns. However, the mechanisms by which water masses gain their patterns are yet to be fully explained. To examine this, we collected water samples along the Extended Ellett Line (EEL), an oceanographic transect between Iceland and Scotland, and measured dissolved REE by offline automated chromatography (SeaFAST) and ICP-MS. The proximity to two continental boundaries, the incipient spring bloom coincident with the timing of the cruise, and the importance of deep water circulation in this climatically sensitive gateway region make it an ideal location to investigate sources of REE to seawater and the effects of vertical cycling and lateral advection on their distribution. The deep waters have REE concentrations closest to typical North Atlantic seawater and are dominated by lateral advection. Comparison to published seawater REE concentrations of the same water masses in other locations provides a first measure of the temporal and spatial stability of the seawater REE signal. We demonstrate the REE pattern is replicated for Iceland-Scotland Overflow Water (ISOW) in the Iceland Basin from adjacent stations sampled 16 years previously. A recently published Labrador Sea Water (LSW) dissolved REE signal is reproduced in the Rockall Trough but shows greater light and mid REE alteration in the Iceland Basin, possibly due to the dominant effect of ISOW and/or continental inputs. An obvious concentration gradient from seafloor sediments to the overlying water column in the Rockall Trough, but not the Iceland Basin, highlights release of light and mid REE from resuspended sediments and pore waters, possibly a seasonal effect associated with the timing of the spring bloom in each basin. The EEL dissolved oxygen minimum at the permanent pycnocline corresponds to positive heavy REE enrichment, indicating maximum rates of organic matter remineralisation and associated REE release. We tentatively suggest a bacterial role to account for the observed heavy REE deviations. This study highlights the need for fully constrained REE sources and sinks, including the temporary nature of some sources, to achieve a balanced budget of seawater REE.
Limnology and Oceanography-methods | 2012
Tina van de Flierdt; Katharina Pahnke; Hiroshi Amakawa; Per Andersson; Chandranath Basak; Barry J. Coles; Christophe Colin; Kirsty C. Crocket; Martin Frank; Norbert Frank; Steven L. Goldstein; Vineet Goswami; Brian A. Haley; Ed C. Hathorne; Sidney R. Hemming; Gideon M. Henderson; Catherine Jeandel; Kevin M. Jones; Katharina Kreissig; Francois Lacan; Myriam Lambelet; Ellen E. Martin; Derrick R Newkirk; Haijme Obata; Leopoldo D Peña; Alexander M. Piotrowski; Catherine Pradoux; Howie D. Scher; Hans Schöberg; Sunil K. Singh
Geochimica et Cosmochimica Acta | 2016
Myriam Lambelet; Tina van de Flierdt; Kirsty C. Crocket; Mark Rehkämper; Katharina Kreissig; Barry J. Coles; Micha J. A. Rijkenberg; Loes J. A. Gerringa; Hein J.W. de Baar; Reiner Steinfeldt
Chemical Geology | 2014
Kirsty C. Crocket; Myriam Lambelet; Tina van de Flierdt; Mark Rehkämper; Laura F. Robinson
Quaternary Science Reviews | 2012
Kirsty C. Crocket; Derek Vance; Gavin L. Foster; David A. Richards; Martyn Tranter
Quaternary Science Reviews | 2013
Kirsty C. Crocket; Gavin L. Foster; Derek Vance; David A. Richards; Martyn Tranter
Chemical Geology | 2017
Torben Struve; Tina van de Flierdt; Andrea Burke; Laura F. Robinson; Samantha J. Hammond; Kirsty C. Crocket; Louisa I. Bradtmiller; Maureen E. Auro; Kais J. Mohamed; Nicholas J. White