Resolving Past Changes in Ocean Oxygenation: Utility of Chromium Isotopes

Lead Research Organisation: University of Leeds
Department Name: School of Earth and Environment

Abstract

There is growing concern that a recent reduction in the concentration of dissolved oxygen in parts of the world's oceans signals a change in the Earth's climate. This is because there is lots of evidence in the geological record that links seawater oxygen to climate change- the anoxic (oxygen deficient) oceans at the end of the Permian (251 million years ago), for example, are associated with global warming and massive extinctions. Nevertheless, what we don't know, is exactly what controls the link between the concentration of dissolved oxygen and climate? Answering this question is extremely difficult because direct measurements of past levels of seawater oxygen, as well as climate parameters such as sea-surface temperature, extend back only as far as a few tens of years. Instead, we must rely on indirect, or so-called 'proxy' measurements that are preserved in the geological record. There are a number of 'proxies' for past levels of seawater oxygen. Most of them rely on measurements of the concentration of metals in marine sediments. However, it is now clear that metal concentrations can be affected by a number of different variables (for example, the level of primary productivity in the overlying water column), all of which can vary independently of seawater oxygen. One way to circumvent some of these problems is by analysis of the isotopes of these metals. In recent times, research has focused on the analysis of iron and molybdenum isotopes, but a key problem is that both iron and molybdenum are insensitive to small changes in seawater oxygen. They are only able to distinguish between oxic (oxygen-replete) or euxinic (no oxygen, high levels of hydrogen sulphide) conditions. For all of these reasons, there is a clear need to find new proxies for seawater oxygen. Chromium is an ideal candidate, for a number of reasons. Firstly, it is soluble under oxic conditions, but insoluble (and therefore accumulates in marine sediments) under slightly oxygen deficient conditions. Second, its isotopes behave very differently under oxic vs oxygen deficient conditions, and this can now be detected using state-of-the-art instrumentation. Third, the chemistry of chromium and its isotopes is relatively simple. The overarching aim of this project is to test the utility of chromium isotopes as a tracer of seawater oxygen. To this end, we will: (1) Measure the chromium isotope composition of marine sediments deposited in a range of oxygen conditions. (2) Determine the precise mechanism of chromium uptake into marine sediments, and the potential for movement of chromium after it has been buried. (3) Obtain records of chromium isotopes for a period of dramatic climate change. We expect the results of our research to provide an improved understanding of the relationships between seawater oxygen and global climate change. Such knowledge will be imperative for both the prediction and mitigation of Earth's climate in the future.

Publications

10 25 50
 
Description We have determined the mode of incorporation of Cr in marine ferromanganese precipitates and carbonates that might be used as records of Cr concentration and stable isotope composition in seawater over the Cenozoic. It is important to understand how Cr becomes enriched in these precipitates because the mechanism of enrichment can cause a fractionation of Cr isotopes that must be separated from the seawater signal recorded in the precipitates. Cr stable isotope signals recorded in marine sediments might give us information about changes in the oxygenation of seawater over the life time of the precipitate, which in turn can tell us about air-sea gas exchange and the evolution of earth's climate.
Exploitation Route Understanding the fate and mobility of toxic Cr(VI) in hyperalkaline wastes like Red Mud Leachates.
Sectors Environment

 
Description We have determined the mode of incorporation of Cr in marine ferromanganese precipitates and carbonates that might be used as records of Cr concentration and stable isotope composition in seawater over the Cenozoic. Work has been used to predict the concentration of heavy metals in rivers and streams following the Ajkai Hungarian Red Mud environmental disaster in 2010. Work has also been used to understand the partitioning of redox sensitive metals between ancient seawater and iron (hhydr)oxides found in Cenozoic marine sediments, to help interpret the chemistry of palaeo seawater and the associated Earth system, for example relating to the PETM event.
First Year Of Impact 2010
Sector Environment
Impact Types Societal,Economic

 
Description Fate of Cr in hyperalkaline wastes 
Organisation University of Leeds
Country United Kingdom 
Sector Academic/University 
PI Contribution Project with Ian Burke at University of Leeds to determine the fate and mobility of Cr in hyperalkaline Red Mud Leachate wastes.
Collaborator Contribution Determine the fate and mobility of toxic oxyanions including arsenic in hyperalkaline Red Mud Leachate wastes.
Impact Lockwood C.L., Mortimer R.J.G., Stewart D.I., Mayes W.M., Peacock C.L., Polya D.A., Lythgoe P.R, Gruiz K.and Burke I.T. (2014) Mobilisation of arsenic from bauxite residue (red mud) affected soils: Effect of pH and redox conditions. Applied Geochemistry, accepted manuscript. Burke I.T., Peacock C.L., Lockwood C.L., Stewart D., Mortimer R., Ward M.B., Renforth P., Gruiz K., Mayes W.M. (2013) Behaviour of aluminium, arsenic and vanadium during the neutralisation of red mud leachate by HCl, gypsum or seawater. Environmental Science and Technology 47, 6527-6535. doi:10.1021/es4010834 Burke I.T., Mayes W.M., Peacock C.L., Brown A.P., Jarvis A.P. and Gruiz K. (2012) Speciation of arsenic, chromium and vanadium in red mud samples from the Ajka spill site, Hungary. Environmental Science and Technology 46, 3085-3092. doi:10.1021/es3003475
Start Year 2011