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Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis)

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Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis). / Hayward, S ; Tani, A ; Owen, S M et al.
In: Tree Physiology, Vol. 24, No. 7, 07.2004, p. 721-728.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Hayward, S, Tani, A, Owen, SM & Hewitt, CN 2004, 'Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis)', Tree Physiology, vol. 24, no. 7, pp. 721-728.

APA

Hayward, S., Tani, A., Owen, S. M., & Hewitt, C. N. (2004). Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis). Tree Physiology, 24(7), 721-728.

Vancouver

Hayward S, Tani A, Owen SM, Hewitt CN. Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis). Tree Physiology. 2004 Jul;24(7):721-728.

Author

Hayward, S ; Tani, A ; Owen, S M et al. / Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis). In: Tree Physiology. 2004 ; Vol. 24, No. 7. pp. 721-728.

Bibtex

@article{2d44608bbe474f79b39df95282bb4479,
title = "Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis)",
abstract = "Volatile organic compound (VOC) emissions from Sitka spruce (Picea sitchensis Bong.) growing in a range of controlled light and temperature regimes were monitored online with a proton transfer reaction-mass spectrometer (PTR-MS) operating at a temporal resolution of similar to1 min. Isoprene emissions accounted for an average of more than 70% of measured VOCs and up to 3.5% of assimilated carbon. Emission rates (E) for isoprene correlated closely with photosynthetic photon flux (PPF) and temperature, showing saturation at a PPF of between 300 and 400 mumol m(-2) s(-1) and a maximum between 35 and 38degreesC. Under standard conditions of 30degreesC and 1000 mumol m(-2) s(-1) PPF, the mean isoprene E was 13 mug g(dm)(-1) h(-1), considerably higher than previously observed in this species. Mean E for acetaldehyde, methanol and monoterpenes at 30degreesC were 0.37,0.78 and 2.97 mug g(dm)(-1) h(-1), respectively. In response to a sudden light to dark transition, isoprene E decreased exponentially by > 98% over about 3 h; however, during the first 7 min, this otherwise steady decay was temporarily but immediately depressed to similar to40% of the pre-darkness rate, before rallying during the following 7 min to rejoin the general downward trajectory of the exponential decay. The sudden sharp fall in isoprene E was mirrored by a burst in acetaldehyde E. The acetaldehyde E maximum coincided with the isoprene E minimum (7 min post-illumination), and ceased when isoprene emissions resumed their exponential decay. The causes of, and linkages between, these phenomena were investigated.",
keywords = "acetaldehyde, isoprene, methanol, monoterpenes, post-illumination burst, post-illumination depression, PTRMS, pyruvate, VOCs, REACTION MASS-SPECTROMETRY, QUERCUS-ILEX L., ISOPRENE EMISSION, TREE LEAVES, TEMPERATURE, LIGHT, MONOTERPENES, ACETALDEHYDE, PLANTS, FIELD",
author = "S Hayward and A Tani and Owen, {S M} and Hewitt, {C. N.}",
year = "2004",
month = jul,
language = "English",
volume = "24",
pages = "721--728",
journal = "Tree Physiology",
issn = "1758-4469",
publisher = "Oxford University Press",
number = "7",

}

RIS

TY - JOUR

T1 - Online analysis of volatile organic compound emissions from Sitka spruce (Picea sitchensis)

AU - Hayward, S

AU - Tani, A

AU - Owen, S M

AU - Hewitt, C. N.

PY - 2004/7

Y1 - 2004/7

N2 - Volatile organic compound (VOC) emissions from Sitka spruce (Picea sitchensis Bong.) growing in a range of controlled light and temperature regimes were monitored online with a proton transfer reaction-mass spectrometer (PTR-MS) operating at a temporal resolution of similar to1 min. Isoprene emissions accounted for an average of more than 70% of measured VOCs and up to 3.5% of assimilated carbon. Emission rates (E) for isoprene correlated closely with photosynthetic photon flux (PPF) and temperature, showing saturation at a PPF of between 300 and 400 mumol m(-2) s(-1) and a maximum between 35 and 38degreesC. Under standard conditions of 30degreesC and 1000 mumol m(-2) s(-1) PPF, the mean isoprene E was 13 mug g(dm)(-1) h(-1), considerably higher than previously observed in this species. Mean E for acetaldehyde, methanol and monoterpenes at 30degreesC were 0.37,0.78 and 2.97 mug g(dm)(-1) h(-1), respectively. In response to a sudden light to dark transition, isoprene E decreased exponentially by > 98% over about 3 h; however, during the first 7 min, this otherwise steady decay was temporarily but immediately depressed to similar to40% of the pre-darkness rate, before rallying during the following 7 min to rejoin the general downward trajectory of the exponential decay. The sudden sharp fall in isoprene E was mirrored by a burst in acetaldehyde E. The acetaldehyde E maximum coincided with the isoprene E minimum (7 min post-illumination), and ceased when isoprene emissions resumed their exponential decay. The causes of, and linkages between, these phenomena were investigated.

AB - Volatile organic compound (VOC) emissions from Sitka spruce (Picea sitchensis Bong.) growing in a range of controlled light and temperature regimes were monitored online with a proton transfer reaction-mass spectrometer (PTR-MS) operating at a temporal resolution of similar to1 min. Isoprene emissions accounted for an average of more than 70% of measured VOCs and up to 3.5% of assimilated carbon. Emission rates (E) for isoprene correlated closely with photosynthetic photon flux (PPF) and temperature, showing saturation at a PPF of between 300 and 400 mumol m(-2) s(-1) and a maximum between 35 and 38degreesC. Under standard conditions of 30degreesC and 1000 mumol m(-2) s(-1) PPF, the mean isoprene E was 13 mug g(dm)(-1) h(-1), considerably higher than previously observed in this species. Mean E for acetaldehyde, methanol and monoterpenes at 30degreesC were 0.37,0.78 and 2.97 mug g(dm)(-1) h(-1), respectively. In response to a sudden light to dark transition, isoprene E decreased exponentially by > 98% over about 3 h; however, during the first 7 min, this otherwise steady decay was temporarily but immediately depressed to similar to40% of the pre-darkness rate, before rallying during the following 7 min to rejoin the general downward trajectory of the exponential decay. The sudden sharp fall in isoprene E was mirrored by a burst in acetaldehyde E. The acetaldehyde E maximum coincided with the isoprene E minimum (7 min post-illumination), and ceased when isoprene emissions resumed their exponential decay. The causes of, and linkages between, these phenomena were investigated.

KW - acetaldehyde

KW - isoprene

KW - methanol

KW - monoterpenes

KW - post-illumination burst

KW - post-illumination depression

KW - PTRMS

KW - pyruvate

KW - VOCs

KW - REACTION MASS-SPECTROMETRY

KW - QUERCUS-ILEX L.

KW - ISOPRENE EMISSION

KW - TREE LEAVES

KW - TEMPERATURE

KW - LIGHT

KW - MONOTERPENES

KW - ACETALDEHYDE

KW - PLANTS

KW - FIELD

M3 - Journal article

VL - 24

SP - 721

EP - 728

JO - Tree Physiology

JF - Tree Physiology

SN - 1758-4469

IS - 7

ER -