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Featured researches published by Srimathy Sriskantharajah.


Proceedings of the Royal Society of London. Series B, Biological Sciences | 2009

Emission of methane from plants

R.E.R Nisbet; R. E. Fisher; R.H Nimmo; Derek S. Bendall; Patrick M. Crill; Angela V. Gallego-Sala; E. R. C. Hornibrook; Enrique López-Juez; D. Lowry; P.B.R Nisbet; E.F Shuckburgh; Srimathy Sriskantharajah; Christopher J. Howe; Euan G. Nisbet

It has been proposed that plants are capable of producing methane by a novel and unidentified biochemical pathway. Emission of methane with an apparently biological origin was recorded from both whole plants and detached leaves. This was the first report of methanogenesis in an aerobic setting, and was estimated to account for 10–45 per cent of the global methane source. Here, we show that plants do not contain a known biochemical pathway to synthesize methane. However, under high UV stress conditions, there may be spontaneous breakdown of plant material, which releases methane. In addition, plants take up and transpire water containing dissolved methane, leading to the observation that methane is released. Together with a new analysis of global methane levels from satellite retrievals, we conclude that plants are not a major source of the global methane production.


Geophysical Research Letters | 2011

Arctic methane sources: Isotopic evidence for atmospheric inputs

R. E. Fisher; Srimathy Sriskantharajah; D. Lowry; M. Lanoisellé; Cathrine Fowler; Rachael H. James; Ove Hermansen; C. Lund Myhre; Andreas Stohl; Jens Greinert; P. B. R. Nisbet-Jones; Jürgen Mienert; Euan G. Nisbet

By comparison of the methane mixing ratio and the carbon isotope ratio (δ13CCH4) in Arctic air with regional background, the incremental input of CH4 in an air parcel and the source δ13CCH4 signature can be determined. Using this technique the bulk Arctic CH4 source signature of air arriving at Spitsbergen in late summer 2008 and 2009 was found to be −68‰, indicative of the dominance of a biogenic CH4 source. This is close to the source signature of CH4 emissions from boreal wetlands. In spring, when wetland was frozen, the CH4 source signature was more enriched in 13C at −53 ± 6‰ with air mass back trajectories indicating a large influence from gas field emissions in the Ob River region. Emissions of CH4 to the water column from the seabed on the Spitsbergen continental slope are occurring but none has yet been detected reaching the atmosphere. The measurements illustrate the significance of wetland emissions. Potentially, these may respond quickly and powerfully to meteorological variations and to sustained climate warming.


Tellus B | 2012

Stable carbon isotope signatures of methane from a Finnish subarctic wetland

Srimathy Sriskantharajah; R. E. Fisher; D. Lowry; Tuula Aalto; Juha Hatakka; Mika Aurela; Tuomas Laurila; Annalea Lohila; E. Kuitunen; Euan G. Nisbet

ABSTRACT Methane emissions from Lompolojänkkä, a Finnish aapa mire within the Arctic Circle, were studied by non-intrusive Keeling plot methods, to place better constraints on the seasonal variations in isotopic signature of methane (δ13CCH4) emitted from Arctic wetland. Air samples were collected in Tedlar bags over the wetland at heights of 42 and 280 cm between May and October 2009 and in August 2008. The mixing ratio and δ13C of the methane in the samples were incorporated into Keeling plot analyses to derive bulk δ13CCH4 signatures for the methane inputs to the air above the wetland. The results show an unexpected consistence in δ13CCH4 from early to late summer, clustered around −68.5±0.7‰, but during spring thaw and autumnal freezing, δ13CCH4 is enriched by approximately 2 and 4‰, respectively. The techniques reported in this paper are simple and economical to employ, and give a bulk source signature for the methane inputs to the air above the entire wetland that can be extrapolated to a larger regional area.


Scientific Reports | 2016

Marked long-term decline in ambient CO mixing ratio in SE England, 1997-2014: evidence of policy success in improving air quality

D. Lowry; M. Lanoisellé; R. E. Fisher; M. Martin; Cathrine Fowler; Iván Y. Hernández-Paniagua; P. C. Novelli; Srimathy Sriskantharajah; P. O’brien; N. D. Rata; C. W. Holmes; Zoe L. Fleming; Kevin C. Clemitshaw; G. Zazzeri; Matthieu Pommier; C. A. McLinden; Euan G. Nisbet

Atmospheric CO at Egham in SE England has shown a marked and progressive decline since 1997, following adoption of strict controls on emissions. The Egham site is uniquely positioned to allow both assessment and comparison of ‘clean Atlantic background’ air and CO-enriched air downwind from the London conurbation. The decline is strongest (approximately 50 ppb per year) in the 1997–2003 period but continues post 2003. A ‘local CO increment’ can be identified as the residual after subtraction of contemporary background Atlantic CO mixing ratios from measured values at Egham. This increment, which is primarily from regional sources (during anticyclonic or northerly winds) or from the European continent (with easterly air mass origins), has significant seasonality, but overall has declined steadily since 1997. On many days of the year CO measured at Egham is now not far above Atlantic background levels measured at Mace Head (Ireland). The results are consistent with MOPITT satellite observations and ‘bottom-up’ inventory results. Comparison with urban and regional background CO mixing ratios in Hong Kong demonstrates the importance of regional, as opposed to local reduction of CO emission. The Egham record implies that controls on emissions subsequent to legislation have been extremely successful in the UK.


Rapid Communications in Mass Spectrometry | 2006

High-precision, automated stable isotope analysis of atmospheric methane and carbon dioxide using continuous-flow isotope-ratio mass spectrometry.

R. E. Fisher; D. Lowry; Owen Wilkin; Srimathy Sriskantharajah; Euan G. Nisbet


Geophysical Research Letters | 2011

Arctic methane sources: Isotopic evidence for atmospheric inputs: ARCTIC METHANE SOURCES

R. E. Fisher; Srimathy Sriskantharajah; D. Lowry; M. Lanoisellé; Cathrine Fowler; Rachael H. James; Ove Hermansen; C. Lund Myhre; Andreas Stohl; Jens Greinert; P. B. R. Nisbet-Jones; Jürgen Mienert; Euan G. Nisbet


Archive | 2010

Isotopic evidence for sources of methane to the Arctic atmosphere in 2008 and 2009

R. E. Fisher; D. Lowry; Srimathy Sriskantharajah; M. Lanoisellé; Mary Glenn Fowler; Euan G. Nisbet


Archive | 2010

Carbon Isotopic Constraints on Arctic Methane Sources, 2008-2010

Ronald E. Fisher; D. Lowry; M. Lanoisellé; Srimathy Sriskantharajah; Euan G. Nisbet


Archive | 2009

London atmospheric Hydrogen and Carbon Monoxide: 12 year record, fluxes, and diurnal studies.

M. Lanoisellé; Ronald E. Fisher; Srimathy Sriskantharajah; D. Lowry; Cathrine Fowler; Euan G. Nisbet


Archive | 2009

Investigating Summer Methane Emissions from Wetlands in Northern Finland and Svalbard

Srimathy Sriskantharajah; Ronald E. Fisher; Cathrine Fowler; Tuula Aalto; Juha Hatakka; D. Lowry; M. Lanoisellé; Euan G. Nisbet

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Andreas Stohl

Norwegian Institute for Air Research

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C. Lund Myhre

Norwegian Institute for Air Research

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Ove Hermansen

Norwegian Institute for Air Research

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