Articles | Volume 11, issue 5
https://doi.org/10.5194/bg-11-1435-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
https://doi.org/10.5194/bg-11-1435-2014
© Author(s) 2014. This work is distributed under
the Creative Commons Attribution 3.0 License.
the Creative Commons Attribution 3.0 License.
Research article
| 
14 Mar 2014
Research article |
| 14 Mar 2014
Laboratory and field measurements of enantiomeric monoterpene emissions as a function of chemotype, light and temperature
W. Song
Max Planck Institut für Chemie, Hahn Meitner Weg 1, 55128 Mainz, Germany
M. Staudt
Centre d'Ecologie Fonctionnelle et Evolutive (UMR5175), 1919 Route de Mende, 34293 Montpellier CEDEX 5, France
I. Bourgeois
Centre d'Ecologie Fonctionnelle et Evolutive (UMR5175), 1919 Route de Mende, 34293 Montpellier CEDEX 5, France
J. Williams
Max Planck Institut für Chemie, Hahn Meitner Weg 1, 55128 Mainz, Germany
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Cited
27 citations as recorded by crossref.
- Enantioselective terpene emission signifies forest climate response mechanism S. Ghosh 10.1016/j.tplants.2023.01.007
- Vibrationally-resolved photoelectron spectroscopy and photoelectron circular dichroism of bicyclic monoterpene enantiomers H. Ganjitabar et al. 10.1016/j.jms.2018.08.007
- Wavelength dependent photoelectron circular dichroism of limonene studied by femtosecond multiphoton laser ionization and electron-ion coincidence imaging M. Rafiee Fanood et al. 10.1063/1.4963229
- Observation and modelling of HO<sub>x</sub> radicals in a boreal forest K. Hens et al. 10.5194/acp-14-8723-2014
- Limonene Enantiomeric Ratios from Anthropogenic and Biogenic Emission Sources S. Gu et al. 10.1021/acs.estlett.3c00794
- Isoprenoid emission response to changing light conditions of English oak, European beech and Norway spruce Y. van Meeningen et al. 10.5194/bg-14-4045-2017
- Circular polarization in atmospheric aerosols S. Gassó & K. Knobelspiesse 10.5194/acp-22-13581-2022
- Selective reagent ion-time of flight-mass spectrometry study of six common monoterpenes D. Materić et al. 10.1016/j.ijms.2017.06.003
- Intense Vibronic Modulation of the Chiral Photoelectron Angular Distribution Generated by Photoionization of Limonene Enantiomers with Circularly Polarized Synchrotron Radiation M. Rafiee Fanood et al. 10.1002/cphc.201701248
- Enantiomer-specific analysis of multi-component mixtures by correlated electron imaging–ion mass spectrometry M. Fanood et al. 10.1038/ncomms8511
- Understanding of formation and change of chiral aroma compounds from tea leaf to tea cup provides essential information for tea quality improvement Y. Zhou et al. 10.1016/j.foodres.2023.112703
- Potential of needle trap microextraction–portable gas chromatography–mass spectrometry for measurement of atmospheric volatile compounds L. Barreira et al. 10.5194/amt-9-3661-2016
- Environmental Factors Affecting Monoterpene Emissions from Terrestrial Vegetation T. Malik et al. 10.3390/plants12173146
- High chemodiversity in the structural and enantiomeric composition of volatiles emitted by Kermes oak populations in Southern France M. Staudt & I. Visnadi 10.1525/elementa.2023.00043
- Chiral monoterpenes reveal forest emission mechanisms and drought responses J. Byron et al. 10.1038/s41586-022-05020-5
- Unraveling the Enantiomeric Distribution of Glycosidically Bound Linalool in Teas (Camellia sinensis) and Their Acidolysis Characteristics and Pyrolysis Mechanism H. Yan et al. 10.1021/acs.jafc.4c00037
- Compartment specific chiral pinene emissions identified in a Maritime pine forest M. Staudt et al. 10.1016/j.scitotenv.2018.11.146
- Gas-phase ozonolysis of β-ocimene: Temperature dependent rate coefficients and product distribution E. Gaona-Colmán et al. 10.1016/j.atmosenv.2016.09.053
- Characterization of α-pinene synthase gene in Pinus pinaster and P. pinea in vitro cultures and differential gene expression following Bursaphelenchus xylophilus inoculation H. Trindade et al. 10.1007/s11738-016-2159-x
- Gardenifolins A–H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line D. Tshitenge et al. 10.1021/acs.jnatprod.7b00180
- New insights into the parametrization of temperature and light responses of mono - and sesquiterpene emissions from Aleppo pine and rosemary M. Staudt et al. 10.1016/j.atmosenv.2016.12.033
- The Tree Drought Emission MONitor (Tree DEMON), an innovative system for assessing biogenic volatile organic compounds emission from plants M. Lüpke et al. 10.1186/s13007-017-0166-6
- Chiral NMR analysis reveals the environmental dependence of areolal scalemization in Piptothrix areolare M. Gómez‐Hurtado et al. 10.1002/chir.23436
- Surprising chiral composition changes over the Amazon rainforest with height, time and season N. Zannoni et al. 10.1038/s43247-020-0007-9
- Plant Secondary Compounds in Soil and Their Role in Belowground Species Interactions B. Ehlers et al. 10.1016/j.tree.2020.04.001
- Enantioselective femtosecond laser photoionization spectrometry of limonene using photoelectron circular dichroism M. Rafiee Fanood et al. 10.1039/C5CP00583C
- Measurement of enantiomer percentages for five monoterpenes from six conifer species by cartridge-tube-based passive sampling adsorption–thermal desorption (ps-ATD) Y. Wang et al. 10.5194/amt-15-4651-2022
27 citations as recorded by crossref.
- Enantioselective terpene emission signifies forest climate response mechanism S. Ghosh 10.1016/j.tplants.2023.01.007
- Vibrationally-resolved photoelectron spectroscopy and photoelectron circular dichroism of bicyclic monoterpene enantiomers H. Ganjitabar et al. 10.1016/j.jms.2018.08.007
- Wavelength dependent photoelectron circular dichroism of limonene studied by femtosecond multiphoton laser ionization and electron-ion coincidence imaging M. Rafiee Fanood et al. 10.1063/1.4963229
- Observation and modelling of HO<sub>x</sub> radicals in a boreal forest K. Hens et al. 10.5194/acp-14-8723-2014
- Limonene Enantiomeric Ratios from Anthropogenic and Biogenic Emission Sources S. Gu et al. 10.1021/acs.estlett.3c00794
- Isoprenoid emission response to changing light conditions of English oak, European beech and Norway spruce Y. van Meeningen et al. 10.5194/bg-14-4045-2017
- Circular polarization in atmospheric aerosols S. Gassó & K. Knobelspiesse 10.5194/acp-22-13581-2022
- Selective reagent ion-time of flight-mass spectrometry study of six common monoterpenes D. Materić et al. 10.1016/j.ijms.2017.06.003
- Intense Vibronic Modulation of the Chiral Photoelectron Angular Distribution Generated by Photoionization of Limonene Enantiomers with Circularly Polarized Synchrotron Radiation M. Rafiee Fanood et al. 10.1002/cphc.201701248
- Enantiomer-specific analysis of multi-component mixtures by correlated electron imaging–ion mass spectrometry M. Fanood et al. 10.1038/ncomms8511
- Understanding of formation and change of chiral aroma compounds from tea leaf to tea cup provides essential information for tea quality improvement Y. Zhou et al. 10.1016/j.foodres.2023.112703
- Potential of needle trap microextraction–portable gas chromatography–mass spectrometry for measurement of atmospheric volatile compounds L. Barreira et al. 10.5194/amt-9-3661-2016
- Environmental Factors Affecting Monoterpene Emissions from Terrestrial Vegetation T. Malik et al. 10.3390/plants12173146
- High chemodiversity in the structural and enantiomeric composition of volatiles emitted by Kermes oak populations in Southern France M. Staudt & I. Visnadi 10.1525/elementa.2023.00043
- Chiral monoterpenes reveal forest emission mechanisms and drought responses J. Byron et al. 10.1038/s41586-022-05020-5
- Unraveling the Enantiomeric Distribution of Glycosidically Bound Linalool in Teas (Camellia sinensis) and Their Acidolysis Characteristics and Pyrolysis Mechanism H. Yan et al. 10.1021/acs.jafc.4c00037
- Compartment specific chiral pinene emissions identified in a Maritime pine forest M. Staudt et al. 10.1016/j.scitotenv.2018.11.146
- Gas-phase ozonolysis of β-ocimene: Temperature dependent rate coefficients and product distribution E. Gaona-Colmán et al. 10.1016/j.atmosenv.2016.09.053
- Characterization of α-pinene synthase gene in Pinus pinaster and P. pinea in vitro cultures and differential gene expression following Bursaphelenchus xylophilus inoculation H. Trindade et al. 10.1007/s11738-016-2159-x
- Gardenifolins A–H, Scalemic Neolignans from Gardenia ternifolia: Chiral Resolution, Configurational Assignment, and Cytotoxic Activities against the HeLa Cancer Cell Line D. Tshitenge et al. 10.1021/acs.jnatprod.7b00180
- New insights into the parametrization of temperature and light responses of mono - and sesquiterpene emissions from Aleppo pine and rosemary M. Staudt et al. 10.1016/j.atmosenv.2016.12.033
- The Tree Drought Emission MONitor (Tree DEMON), an innovative system for assessing biogenic volatile organic compounds emission from plants M. Lüpke et al. 10.1186/s13007-017-0166-6
- Chiral NMR analysis reveals the environmental dependence of areolal scalemization in Piptothrix areolare M. Gómez‐Hurtado et al. 10.1002/chir.23436
- Surprising chiral composition changes over the Amazon rainforest with height, time and season N. Zannoni et al. 10.1038/s43247-020-0007-9
- Plant Secondary Compounds in Soil and Their Role in Belowground Species Interactions B. Ehlers et al. 10.1016/j.tree.2020.04.001
- Enantioselective femtosecond laser photoionization spectrometry of limonene using photoelectron circular dichroism M. Rafiee Fanood et al. 10.1039/C5CP00583C
- Measurement of enantiomer percentages for five monoterpenes from six conifer species by cartridge-tube-based passive sampling adsorption–thermal desorption (ps-ATD) Y. Wang et al. 10.5194/amt-15-4651-2022
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