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Real-time visualisation and quantification of PAH photodegradation on and within plant leaves.

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Real-time visualisation and quantification of PAH photodegradation on and within plant leaves. / Wild, Edward; Dent, John; Thomas, Gareth O. et al.
In: Environmental Science and Technology, Vol. 39, No. 1, 01.01.2005, p. 268-273.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

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Wild E, Dent J, Thomas GO, Jones KC. Real-time visualisation and quantification of PAH photodegradation on and within plant leaves. Environmental Science and Technology. 2005 Jan 1;39(1):268-273. doi: 10.1021/es0494196

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Wild, Edward ; Dent, John ; Thomas, Gareth O. et al. / Real-time visualisation and quantification of PAH photodegradation on and within plant leaves. In: Environmental Science and Technology. 2005 ; Vol. 39, No. 1. pp. 268-273.

Bibtex

@article{748fc553e3394bcaa461a3ff6dd0a4af,
title = "Real-time visualisation and quantification of PAH photodegradation on and within plant leaves.",
abstract = "Vegetation plays a key role in the environmental cycling and fate of many organic chemicals. A compound's location on or within leaves will affect its persistence and significance; retention in surface compartments (i.e., the epicuticular wax and cuticle) renders the compound more susceptible to photodegradation and volatilization, while penetration into the epidermal cell walls or cytoplasm will enhance susceptibility to metabolism. Here, for the first time, methodologies which combine plant and PAH autofluorescence with two-photon excitation microscopy (TPEM) are used to visualize and quantify compound photodegradation on and within living plant leaves. Anthracene, fluoranthene, and phenanthrene were introduced to living leaves of Zea mays and monitored in real time, in control treatments, and when subject to UV-A radiation. Compound photodegradation was observed directly; different degradation rates occurred for different compounds (anthracene > fluoranthene > phenanthrene) and in different locations (at the leaf surface > within the epidermal cells). Results suggest that photodegradation on vegetation may be a more important loss mechanism for PAHs than previously thought. Compound fate in vegetation is potentially highly complex, influenced by diffusion into and location within leaf structures, the rates of supply/loss with the atmosphere, exposure to sunlight, and other environmental conditions. The techniques described here provide a real-time tool to advance insight into these issues.",
author = "Edward Wild and John Dent and Thomas, {Gareth O.} and Jones, {Kevin C.}",
year = "2005",
month = jan,
day = "1",
doi = "10.1021/es0494196",
language = "English",
volume = "39",
pages = "268--273",
journal = "Environmental Science and Technology",
issn = "0013-936X",
publisher = "American Chemical Society",
number = "1",

}

RIS

TY - JOUR

T1 - Real-time visualisation and quantification of PAH photodegradation on and within plant leaves.

AU - Wild, Edward

AU - Dent, John

AU - Thomas, Gareth O.

AU - Jones, Kevin C.

PY - 2005/1/1

Y1 - 2005/1/1

N2 - Vegetation plays a key role in the environmental cycling and fate of many organic chemicals. A compound's location on or within leaves will affect its persistence and significance; retention in surface compartments (i.e., the epicuticular wax and cuticle) renders the compound more susceptible to photodegradation and volatilization, while penetration into the epidermal cell walls or cytoplasm will enhance susceptibility to metabolism. Here, for the first time, methodologies which combine plant and PAH autofluorescence with two-photon excitation microscopy (TPEM) are used to visualize and quantify compound photodegradation on and within living plant leaves. Anthracene, fluoranthene, and phenanthrene were introduced to living leaves of Zea mays and monitored in real time, in control treatments, and when subject to UV-A radiation. Compound photodegradation was observed directly; different degradation rates occurred for different compounds (anthracene > fluoranthene > phenanthrene) and in different locations (at the leaf surface > within the epidermal cells). Results suggest that photodegradation on vegetation may be a more important loss mechanism for PAHs than previously thought. Compound fate in vegetation is potentially highly complex, influenced by diffusion into and location within leaf structures, the rates of supply/loss with the atmosphere, exposure to sunlight, and other environmental conditions. The techniques described here provide a real-time tool to advance insight into these issues.

AB - Vegetation plays a key role in the environmental cycling and fate of many organic chemicals. A compound's location on or within leaves will affect its persistence and significance; retention in surface compartments (i.e., the epicuticular wax and cuticle) renders the compound more susceptible to photodegradation and volatilization, while penetration into the epidermal cell walls or cytoplasm will enhance susceptibility to metabolism. Here, for the first time, methodologies which combine plant and PAH autofluorescence with two-photon excitation microscopy (TPEM) are used to visualize and quantify compound photodegradation on and within living plant leaves. Anthracene, fluoranthene, and phenanthrene were introduced to living leaves of Zea mays and monitored in real time, in control treatments, and when subject to UV-A radiation. Compound photodegradation was observed directly; different degradation rates occurred for different compounds (anthracene > fluoranthene > phenanthrene) and in different locations (at the leaf surface > within the epidermal cells). Results suggest that photodegradation on vegetation may be a more important loss mechanism for PAHs than previously thought. Compound fate in vegetation is potentially highly complex, influenced by diffusion into and location within leaf structures, the rates of supply/loss with the atmosphere, exposure to sunlight, and other environmental conditions. The techniques described here provide a real-time tool to advance insight into these issues.

U2 - 10.1021/es0494196

DO - 10.1021/es0494196

M3 - Journal article

VL - 39

SP - 268

EP - 273

JO - Environmental Science and Technology

JF - Environmental Science and Technology

SN - 0013-936X

IS - 1

ER -