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Dive into the research topics where Andy Ridgwell is active.

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Featured researches published by Andy Ridgwell.


Nature | 2000

Effect of iron supply on Southern Ocean CO2 uptake and implications for glacial atmospheric CO2

Andrew J. Watson; D. C. E. Bakker; Andy Ridgwell; Philip W. Boyd; C. S. Law

Photosynthesis by marine phytoplankton in the Southern Ocean, and the associated uptake of carbon, is thought to be currently limited by the availability of iron. One implication of this limitation is that a larger iron supply to the region in glacial times could have stimulated algal photosynthesis, leading to lower concentrations of atmospheric CO 2. Similarly, it has been proposed that artificial iron fertilization of the oceans might increase future carbon sequestration. Here we report data from a whole-ecosystem test of the iron-limitation hypothesis in the Southern Ocean, which show that surface uptake of atmospheric CO 2 and uptake ratios of silica to carbon by phytoplankton were strongly influenced by nanomolar increases of iron concentration. We use these results to inform a model of global carbon and ocean nutrients, forced with atmospheric iron fluxes to the region derived from the Vostok ice-core dust record. During glacial periods, predicted magnitudes and timings of atmospheric CO2 changes match ice-core records well. At glacial terminations, the model suggests that forcing of Southern Ocean biota by iron caused the initial ∼40 p.p.m. of glacial–interglacial CO2 change, but other mechanisms must have accounted for the remaining 40 p.p.m. increase. The experiment also confirms that modest sequestration of atmospheric CO2 by artificial additions of iron to the Southern Ocean is in principle possible, although the period and geographical extent over which sequestration would be effective remain poorly known.


Nature | 2012

A Cenozoic record of the equatorial Pacific carbonate compensation depth

Heiko Pälike; Mitchell Lyle; Hiroshi Nishi; Isabella Raffi; Andy Ridgwell; Kusali Gamage; Adam Klaus; Gary D Acton; Louise Anderson; Jan Backman; Jack G. Baldauf; Catherine Beltran; Steven M. Bohaty; Paul R. Bown; W.H. Busch; James E T Channell; Cecily O. J. Chun; Margaret Lois Delaney; Pawan Dewangan; Tom Dunkley Jones; Kirsty M. Edgar; Helen F Evans; Peter Fitch; Gavin L. Foster; Nikolaus Gussone; Hitoshi Hasegawa; Ed C. Hathorne; Hiroki Hayashi; Jens O. Herrle; Ann Holbourn

Atmospheric carbon dioxide concentrations and climate are regulated on geological timescales by the balance between carbon input from volcanic and metamorphic outgassing and its removal by weathering feedbacks; these feedbacks involve the erosion of silicate rocks and organic-carbon-bearing rocks. The integrated effect of these processes is reflected in the calcium carbonate compensation depth, which is the oceanic depth at which calcium carbonate is dissolved. Here we present a carbonate accumulation record that covers the past 53 million years from a depth transect in the equatorial Pacific Ocean. The carbonate compensation depth tracks long-term ocean cooling, deepening from 3.0–3.5 kilometres during the early Cenozoic (approximately 55 million years ago) to 4.6 kilometres at present, consistent with an overall Cenozoic increase in weathering. We find large superimposed fluctuations in carbonate compensation depth during the middle and late Eocene. Using Earth system models, we identify changes in weathering and the mode of organic-carbon delivery as two key processes to explain these large-scale Eocene fluctuations of the carbonate compensation depth.


Geology | 2008

Sedimentary response to Paleocene-Eocene Thermal Maximum carbon release: A model-data comparison

Km Panchuk; Andy Ridgwell; Lee R. Kump

Possible sources of carbon that may have caused global warming at the Paleocene-Eocene boundary are constrained using an intermediate complexity Earth-system model confi gured with early Eocene paleogeography. We fi that 6800 Pg C (δ 13 C of -22‰) is the smallest pulse modeled here to reasonably reproduce observations of the extent of seafl oor CaCO 3 dis- solution. This pulse could not have been solely the result of methane hydrate destabilization, suggesting that additional sources of CO 2 such as volcanic CO 2 , the oxidation of sedimentary organic carbon, or thermogenic methane must also have contributed. Observed contrasts in dissolution intensity between Atlantic and Pacifi c sites are reproduced in the model by reduc- ing bioturbation in the Atlantic during the event, simulating a potential consequence of the spread of low-oxygen bottom waters.


Global Biogeochemical Cycles | 1999

Consumption of atmospheric methane by soils: A process‐based model

Andy Ridgwell; Stewart Marshall; Keith Gregson

A process-based model for the consumption of atmospheric methane (CH4) by soils was developed to identify the most important factors affecting uptake rates and to determine whether the current uncertainties in the estimated size of the global soil sink might be reduced. Descriptions of diffusion and microbial oxidation processes, which together determine the CH4 flux, were included. The results suggest that the global sink strength lies within the range 20–51 Tg yr−1 CH4, with a preferred value of 38 Tg yr−1 CH4. Dry tropical ecosystems account for almost a third of this total. Here microbial activity rather than diffusion is limiting uptake. It is also in these areas that the impact of any intensification in agriculture will be the most pronounced, with a possible future reduction in uptake in excess of 3 Tg yr−1 CH4. This is in contrast to the overall impact of global warming, which is expected to leave the size of the global soil sink relatively unchanged.


Journal of Climate | 2013

Long-Term Climate Change Commitment and Reversibility: An EMIC Intercomparison

Kirsten Zickfeld; Michael Eby; Andrew J. Weaver; Kaitlin Alexander; Elisabeth Crespin; Neil R. Edwards; A. V. Eliseev; Georg Feulner; Thierry Fichefet; Chris E. Forest; Pierre Friedlingstein; Hugues Goosse; Philip B. Holden; Fortunat Joos; Michio Kawamiya; David W. Kicklighter; Hendrik Kienert; Katsumi Matsumoto; I. I. Mokhov; Erwan Monier; Steffen M. Olsen; Jens Olaf Pepke Pedersen; Mahe Perrette; Gwenaëlle Philippon-Berthier; Andy Ridgwell; Adam Schlosser; Thomas Schneider von Deimling; Gary Shaffer; Andrei P. Sokolov; Renato Spahni

AbstractThis paper summarizes the results of an intercomparison project with Earth System Models of Intermediate Complexity (EMICs) undertaken in support of the Intergovernmental Panel on Climate Change (IPCC) Fifth Assessment Report (AR5). The focus is on long-term climate projections designed to 1) quantify the climate change commitment of different radiative forcing trajectories and 2) explore the extent to which climate change is reversible on human time scales. All commitment simulations follow the four representative concentration pathways (RCPs) and their extensions to year 2300. Most EMICs simulate substantial surface air temperature and thermosteric sea level rise commitment following stabilization of the atmospheric composition at year-2300 levels. The meridional overturning circulation (MOC) is weakened temporarily and recovers to near-preindustrial values in most models for RCPs 2.6–6.0. The MOC weakening is more persistent for RCP8.5. Elimination of anthropogenic CO2 emissions after 2300 resu...


Philosophical Transactions of the Royal Society A | 2010

Gas hydrates: past and future geohazard?

Mark A. Maslin; Matthew Owen; Richard A. Betts; Simon Day; Tom Dunkley Jones; Andy Ridgwell

Gas hydrates are ice-like deposits containing a mixture of water and gas; the most common gas is methane. Gas hydrates are stable under high pressures and relatively low temperatures and are found underneath the oceans and in permafrost regions. Estimates range from 500 to 10 000 giga tonnes of carbon (best current estimate 1600–2000 GtC) stored in ocean sediments and 400 GtC in Arctic permafrost. Gas hydrates may pose a serious geohazard in the near future owing to the adverse effects of global warming on the stability of gas hydrate deposits both in ocean sediments and in permafrost. It is still unknown whether future ocean warming could lead to significant methane release, as thermal penetration of marine sediments to the clathrate–gas interface could be slow enough to allow a new equilibrium to occur without any gas escaping. Even if methane gas does escape, it is still unclear how much of this could be oxidized in the overlying ocean. Models of the global inventory of hydrates and trapped methane bubbles suggest that a global 3°C warming could release between 35 and 940 GtC, which could add up to an additional 0.5°C to global warming. The destabilization of gas hydrate reserves in permafrost areas is more certain as climate models predict that high-latitude regions will be disproportionately affected by global warming with temperature increases of over 12°C predicted for much of North America and Northern Asia. Our current estimates of gas hydrate storage in the Arctic region are, however, extremely poor and non-existent for Antarctica. The shrinking of both the Greenland and Antarctic ice sheets in response to regional warming may also lead to destabilization of gas hydrates. As ice sheets shrink, the weight removed allows the coastal region and adjacent continental slope to rise through isostacy. This removal of hydrostatic pressure could destabilize gas hydrates, leading to massive slope failure, and may increase the risk of tsunamis.


Geology | 2008

Biogeochemical controls on photic-zone euxinia during the end-Permian mass extinction

Karin Meyer; Lee R. Kump; Andy Ridgwell

Geochemical, biomarker, and isotopic evidence suggests that the end-Permian was characterized by extreme oceanic anoxia that may have led to hydrogen sulfide buildup and mass extinction. We use an earth system model to quantify the biogeochemical and physical conditions necessary for widespread oceanic euxinia and hydrogen sulfide release to the atmosphere. Greater than threefold increases in ocean nutrient content combined with nutrient-trapping ocean circulation cause surface-water H 2 S accumulation in the paleo–Tethys Ocean and in areas of strong upwelling. Accounting for the presence of sulfide-oxidizing phototrophs in the model suppresses but does not prevent widespread release of H 2 S to the atmosphere. Evidence from the geologic record is consistent with modeled geochemical distributions of widespread nutrient-induced euxinia during the end-Permian, suggesting H 2 S toxicity and hypercapnia may have provided the kill mechanism for extinction.


Geological Society, London, Special Publications | 2005

Mid-Pleistocene revolution and the 'eccentricity myth'

Mark A. Maslin; Andy Ridgwell

Abstract The mid-Pleistocene revolution (MPR) is the term used to describe the transition between 41 ka and 100 ka glacial-interglacial cycles which occurred about one million years ago. Despite eccentricity having by far the weakest influence on insolation received at the Earth’s surface of any of the orbital parameters, it is often assumed to be the primary driver of the post-MPR 100 ka climate cycles. The traditional solution to this is to call for a highly nonlinear response by the global climate system to eccentricity. This ‘eccentricity myth’ is a simplified view of the relationship between global climate and orbital forcing and is in part due to an artefact of spectral analysis. Our aim here is to clarify the often confused role of eccentricity and review current theories of the MPR. We suggest that the post-MPR ‘100 ka’ glacial-interglacial cycles are more closely linked to precession, with the saw-toothed climate cycles being defined by every four or five precessional cycle. Because control over the number of precessional cycles involved is determined by eccentricity, eccentricity at most paces rather than drives the system. If true, then one must also question whether the MPR, itself defined by an abrupt change in spectral characteristics, is not also somewhat misconceived.


Nature | 2012

Potential methane reservoirs beneath Antarctica

Jemma L. Wadham; Sandra Arndt; Slawek Tulaczyk; Marek Stibal; Martyn Tranter; Jon Telling; Grzegorz P. Lis; Emily C. Lawson; Andy Ridgwell; Ashley Dubnick; Martin Sharp; Alexandre M. Anesio; Catriona Butler

Once thought to be devoid of life, the ice-covered parts of Antarctica are now known to be a reservoir of metabolically active microbial cells and organic carbon. The potential for methanogenic archaea to support the degradation of organic carbon to methane beneath the ice, however, has not yet been evaluated. Large sedimentary basins containing marine sequences up to 14 kilometres thick and an estimated 21,000 petagrams (1 Pg equals 1015 g) of organic carbon are buried beneath the Antarctic Ice Sheet. No data exist for rates of methanogenesis in sub-Antarctic marine sediments. Here we present experimental data from other subglacial environments that demonstrate the potential for overridden organic matter beneath glacial systems to produce methane. We also numerically simulate the accumulation of methane in Antarctic sedimentary basins using an established one-dimensional hydrate model and show that pressure/temperature conditions favour methane hydrate formation down to sediment depths of about 300 metres in West Antarctica and 700 metres in East Antarctica. Our results demonstrate the potential for methane hydrate accumulation in Antarctic sedimentary basins, where the total inventory depends on rates of organic carbon degradation and conditions at the ice-sheet bed. We calculate that the sub-Antarctic hydrate inventory could be of the same order of magnitude as that of recent estimates made for Arctic permafrost. Our findings suggest that the Antarctic Ice Sheet may be a neglected but important component of the global methane budget, with the potential to act as a positive feedback on climate warming during ice-sheet wastage.


Science | 2013

Marine Ecosystem Responses to Cenozoic Global Change

Richard D. Norris; S. Kirtland Turner; Pincelli M. Hull; Andy Ridgwell

The future impacts of anthropogenic global change on marine ecosystems are highly uncertain, but insights can be gained from past intervals of high atmospheric carbon dioxide partial pressure. The long-term geological record reveals an early Cenozoic warm climate that supported smaller polar ecosystems, few coral-algal reefs, expanded shallow-water platforms, longer food chains with less energy for top predators, and a less oxygenated ocean than today. The closest analogs for our likely future are climate transients, 10,000 to 200,000 years in duration, that occurred during the long early Cenozoic interval of elevated warmth. Although the future ocean will begin to resemble the past greenhouse world, it will retain elements of the present “icehouse” world long into the future. Changing temperatures and ocean acidification, together with rising sea level and shifts in ocean productivity, will keep marine ecosystems in a state of continuous change for 100,000 years.

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Lee R. Kump

Pennsylvania State University

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Mark A. Maslin

University College London

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