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研究领域

My research interest is the production of biogenic trace gases in marine environments. Marine algae are a source of volatile organohalogens (e.g. methyl iodide), non-methane hydrocarbons (e.g. ethene, isoprene) and the sulphur gas dimethyl sulphide (DMS). These compounds can affect atmospheric processes after sea-to-air transfer. Over the last 30 years, much research has focused on the production of DMS. This volatile compound plays a major role in the biogeochemical cycling of sulphur, influences atmospheric acidity and is thought to affect climate through the production of cloud condensation nuclei. The precursor of DMS is dimethylsulphoniopropionate (DMSP), a compatible solute found in the cells of some types of marine phytoplankton and seaweeds, but the conversion of DMSP to DMS occurs via a network of processes within the marine microbial foodweb. The ecology of traces gases in the infochemistry of phytoplankton The production of DMS is greatly increased by biological interactions including grazing. Since the background concentrations of DMS are low (nanomolar range), grazing by herbivorous flagellates and ciliates results in distinct gas signatures that could provide a directional cue to carnivorous mesozooplankton including copepods and krill. Potentially, DMS and other gases can mediate the tritrophic interactions between small phytoplankton, herbivorous protists and larger zooplankton. Analogous interactions between plants, herbivores and carnivores are well described for terrestrial examples, where the production of trace gases by the plant indirectly reduces the grazing pressure from herbivores. It is likely that such interactions exist in the pelagic realm but this has not been demonstrated in any aquatic environment. Chemodetection of DMS in microzooplankton, copepods and krill We use behavioural filming, microcapillary assays and particle-image velocimetry (PIV) to investigate the swimming behaviour of microzooplankton, copepods and krill when exposed to gradients of DMS and DMSP. Our work indicted that copepods and krill have the sensory capability to perceive gradients of DMS. This suggests that DMS is much more than a trace gas with climatic consequences but that it is an infochemical that affects the behaviour of zooplankton and could alter the ecology of predator-prey relationships. Metabolic pathways for DMSP-dependent DMS-production Despite its overall importance for climate, the production of DMS is still somewhat of a mystery. Our recent work focussed on the production of DMS in bacteria where we identified a novel pathway for DMSP-dependent DMS-production. Previous work on axenic phytoplankton cultures demonstrated that algae are capable of direct DMS production, however, molecular genetic evidence for this is still lacking. We are now using proteomic and transgenic approaches to unravel the molecular details of DMS release in the coccolithophore Emiliania huxleyi. The ecophysiology of biogenic trace gases under future CO2 levels Many of the marine trace gases affect climate through the formation of cloud condensation nuclei in the atmosphere or the destruction of tropospheric ozone. Man’s unwavering reliance on the combustion of fossil fuels, combined with activities including deforestation and cement production, has resulted in ever-increasing atmospheric CO2 concentrations. Part of this additional CO2 dissolves in the surface oceans where it leads to ocean acidification. The effect of ocean acidification on trace gas production is not well understood and we participated in recent field-mesocosm experiments that provided a first insight into the role of future CO2 levels on the concentrations of DMS and organohalogens. We are currently participating in turbidostat-mesocosm experiments that study acclimated cultures of Emiliania huxleyi under present and future CO2 levels. The role of DMSP and related compounds in the stress-physiology of zooxanthellae-cnidarian symbioses Coral reefs are hotspots for the production of DMSP and DMS. Virtually all of this is produced by autotrophic dinoflagellates from the genus Symbiodinium (zooxanthellae) that live symbiotically with many marine invertebrates including sea anemones and corals. The exact biological reason for DMSP and DMS production is unknown but they may assist with the scavenging of harmful Reactive Oxygen Species (ROS), so may function as antioxidants in algae. Indeed, our studies with isolated Symbiodinium suggest a close link between DMS production and temperature- and light-induced oxidative stress. Some Symbiodinium genotypes are better adapted to high oxidative stress than others. Is their ability to produce DMS-antioxidants related to the susceptibility of Symbiodinium-coral relationships to stress? Production of dimethyl sulphide (DMS) and isoprene in coral reef ecosystems We recently started adapting a Fast Isoprene Sensor (FIS) for our work on aquatic samples. This sensor is being used in the field and in the laboratory in combination with the conventional gas chromatographic techniques to monitor production of DMS and isoprene in various environments including temperate estuaries and tropical coral reefs. Our first field test at a coral reef in Indonesia was successful and revealed specific patterns of isoprene release from various coral species. In higher plants, isoprene is produced in response to thermal stress and likely assists with membrane functioning. Further work will focus on the dynamics of isoprene release under various environmental conditions. Production of ethene (ethylene) in marine algae and its possible function as an infochemical Ethene is a gaseous plant “hormone” that is of critical importance for the flower and fruit development in higher plants. We demonstrated that the marine seaweed Ulva (Enteromorpha) intestinalis produces ethene via the same metabolic pathway described for terrestrial plants. Physiological experiments showed that light stress can greatly enhance the co-release of ethene with DMS. However, whether ethene plays a role in the light acclimation process, for example via the induction of de-novo synthesis of protective pigments, is unknown.

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Beddow, J., B. Stolpe, P.A. Cole, J.R. Lead, M. Sapp, B.P. Lyons, B. McKew, M. Steinke, F. Benyahia, I. Colbeck, C. Whitby (2014). Estuarine sediment hydrocarbon-degrading microbial communities demonstrate resilience to nanosilver. International Journal of Biodeterioration and Biodegradation 96: 206-215; doi:10.1016/j.ibiod.2014.09.004 Borell, E.M., M. Steinke, R. Horwitz, M. Fine. 2014. Increasing pCO2 correlates with low concentrations of intracellular dimethylsulfoniopropionate in the sea anemone Anemonia viridis. Ecology and Evolution 4: 441-449; doi:10.1002/ece3.946 Brodie, J., C. Williamson, D.A. Smale, N. Kamenos, N. Mieszkowska, R. Santos, M. Cunliffe, M. Steinke, C. Yesson, K.M. Anderson, V. Asnaghi, C. Brownlee, H. Burdett, M. Burrows, S. Collins, P. Donohughe, B. Harvey, A. Foggo, F. Noisette, J. Nunes, F. Ragazzola, J. Raven, D.N. Schmidt, D. Suggett, M. Teichberg, J.M. Hall-Spencer (2014) The future of the NE Atlantic benthic flora in a high CO2 world. Ecology and Evolution 4(13): 2787-2798; doi: 10.1002/ece3.1105 Exton, D.A., T.J. McGenity, M. Steinke, D.J. Smith, D.J. Suggett 2014. Uncovering the volatile nature of tropical coastal marine ecosystems in a changing world. Global Change Biology, in press; doi: 10.1111/gcb.12764 Rinnan, R., M. Steinke, T. McGenity, F. Loreto. 2014. Plant volatiles in extreme terrestrial and marine environments. Plant Cell and Environment 37: 1776-1789; doi: 10.1111/pce.12320 Arnold H.E, P.D. Kerrison, M. Steinke. 2013. Interacting effects of ocean acidification and warming on growth and DMS-production in the haptophyte coccolithophore Emiliania huxleyi. Global Change Biology 19: 1007-1016; doi: 10.1111/gcb.12105. Borell, E.M., M. Steinke, M. Fine. 2013. Direct and indirect effects of high pCO2 on algal grazing by coral reef herbivores from the Gulf of Aqaba (Red Sea). Coral Reefs; doi: 10.1007/s00338-013-1066-5 Breckels, M.N., N.W.F. Bode, E.A. Codling, M. Steinke. 2013. The effect of grazing-mediated DMS production on the behavior of the copepod Calanus helgolandicus. Marine Drugs 11: 2486-2500; doi:10.3390/md11072486 Exton D.A., D.J. Suggett, T.J. McGenity, M. Steinke. 2013. Chlorophyll-normalized isoprene production in laboratory cultures of marine microalgae and implications for global models. Limnology and Oceanography 58(4): 1301-1311; doi: 10.4319/lo.2013.58.4.1301 Lewis, N.D., A. Morozov, M.N. Breckels, M. Steinke, E.A. Codling. 2013. Multitrophic Interactions in the Sea: Assessing the Effect of Infochemical-Mediated Foraging in a 1-d Spatial Model. Mathematical Modelling of Natural Phenomena 8(6): 32–51; doi:10.1051/mmnp/20138602 Lewis, N.D., M.N. Breckels, M. Steinke, E.A. Codling. 2013. Role of infochemical mediated zooplankton grazing in a phytoplankton competition model. Ecological Complexity, doi:10.1016/j.ecocom.2012.10.003. Avgoustidi, V., P. Nightingale, I. Joint, M. Steinke, S. Turner and P. Liss (2012) Decreased marine dimethyl sulfide production under elevated CO2 levels in mesocosm and in vitro studies. Environmental Chemistry: 9: 399-404 Bell, T.G., G. Malin, G.A. Lee, J. Stefels, S. Archer, M. Steinke, P. Matrai (2012) Global Oceanic DMS Data Inter-Comparability. Biogeochemistry 110: 147-161; doi:10.1007/s10533-011-9662-3 Caruana A.M.N., M. Steinke, S. Turner, G. Malin (2012) Concentrations of dimethylsulfoniopropionate and activities of dimethylsulfide-producing enzymes in batch cultures of nine dinoflagellate species. Biogeochemistry 110: 87-107. doi:10.1007/s10533-012-9705-4 Exton D.A., D.J. Suggett, M. Steinke, T.J. McGenity (2012) Spatial and temporal variability of biogenic isoprene emissions from a temperate estuary. Global Biogeochemical Cycles 26(2): GB2012. doi:10.1029/2011GB004210 Green B.C., D.J. Suggett, A. Hills, M. Steinke (2012) Optimisation of a Fast DMS Sensor (FDS) for real time quantification of dimethyl sulphide production by algae. Biogeochemistry 110: 163-172. doi:10.1007/s10533-011-9678-8 Kerrison, P., D.J. Suggett, L.J. Hepburn, M. Steinke (2012) Effect of elevated pCO2 on the production of dimethylsulphoniopropionate (DMSP) and dimethyl sulphide (DMS) in two species of Ulva (Chlorophyceae). Biogeochemistry 110: 5-16. doi:10.1007/s10533-012-9707-2 Lewis, N.D., M.N. Breckels, S.D. Archer, A. Morozov, J.W. Pitchford, M. Steinke, E.A. Codling (2012) Grazing-induced production of DMS can stabilize food-web dynamics and promote the formation of phytoplankton blooms in a multitrophic plankton model. Biogeochemistry 110: 303-313; doi:10.1007/s10533-011-9649-0 Boakes, D.E., E.A. Codling, G.J. Thorn, M. Steinke (2011) Analysis and Modelling of Swimming Behaviour in Oxyrrhis marina. Journal of Plankton Research 33(4): 641-649; doi:10.1093/plankt/fbq136 PDF Breckels M.N., E.C. Roberts, S.D. Archer, G. Malin, M. Steinke (2011) The role of dissolved infochemicals in the ecology of the heterotrophic dinoflagellate Oxyrrhis marina. Journal of Plankton Research 33(4): 629-639; doi:10.1093/plankt/fbq114 PDF

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