A review and synthesis of monoterpene speciation from forests in the United States

The monoterpene composition (emission and tissue internal concentration) of major forest tree species in the United States is discussed. Of the 14 most commonly occurring compounds (α-pinene, β-pinene, Δ3-carene, d-limonene, camphene, myrcene, α-terpinene, β-phellandrene, sabinene, ρ-cymene, ocimene, α-thujene, terpinolene, and γ-terpinene), the first six are usually found to be most abundant. Expected regional variability based on the monoterpene composition fingerprints and corresponding tree species distribution and abundance is examined. In the southeast, a-pinene and β-pinene seem to dominate monoterpene emissions, while in the northern forests emissions are distributed more evenly among the six major compounds. In some parts of western forests, β-pinene and Δ3-carene can be more abundant than α-pinene. Among the other eight compounds, β-phellandrene and sabinene occasionally are significant percentages of expected local monoterpene emissions. Ocimene and ρ-cymene are estimated to be more common in regions dominated by deciduous broadleaf forests, although total emission rates are generally lower for these forests relative to those dominated by conifers. These percentages are compared with monoterpene composition measured in ambient air at various sites. Estimated monoterpene emission composition based on local forest species composition agrees fairly well with ambient measurements for the six major compounds. The past assumption that α-pinene composes approximately 50% of total monoterpene emissions appears reasonable for many areas, except for possibly the northern coniferous forests and some areas in the west dominated by true firs, spruce, and western pines (lodgepole and ponderosa pines). The oxygenated monoterpenes such as camphor, bornyl acetate, and cineole often compose high percentages of the monoterpenes within plant tissues, but are much less abundant in emission samples. Even after adjusting for lower vapor pressures of these compounds, emission rates relative to the hydrocarbon monoterpenes are often lower than would be expected from their internal concentrations. More study is warranted on monoterpene emission rates and composition, especially from the spruces, true firs, hemlocks, cedars, and some deciduous species such as the maples. Non-invasive canopy level and whole ecosystem flux studies are also needed to establish uncertainty estimates for monoterpene emission models. © 2000 Elsevier Science Ltd. All rights reserved

A review and synthesis of monoterpene speciation from forests in the United States

The monoterpene composition (emission and tissue internal concentration) of major forest tree species in the United States is discussed. Of the 14 most commonly occurring compounds (α-pinene, β-pinene, Δ3-carene, d-limonene, camphene, myrcene, α-terpinene, β-phellandrene, sabinene, ρ-cymene, ocimene, α-thujene, terpinolene, and γ-terpinene), the first six are usually found to be most abundant. Expected regional variability based on the monoterpene composition fingerprints and corresponding tree species distribution and abundance is examined. In the southeast, a-pinene and β-pinene seem to dominate monoterpene emissions, while in the northern forests emissions are distributed more evenly among the six major compounds. In some parts of western forests, β-pinene and Δ3-carene can be more abundant than α-pinene. Among the other eight compounds, β-phellandrene and sabinene occasionally are significant percentages of expected local monoterpene emissions. Ocimene and ρ-cymene are estimated to be more common in regions dominated by deciduous broadleaf forests, although total emission rates are generally lower for these forests relative to those dominated by conifers. These percentages are compared with monoterpene composition measured in ambient air at various sites. Estimated monoterpene emission composition based on local forest species composition agrees fairly well with ambient measurements for the six major compounds. The past assumption that α-pinene composes approximately 50% of total monoterpene emissions appears reasonable for many areas, except for possibly the northern coniferous forests and some areas in the west dominated by true firs, spruce, and western pines (lodgepole and ponderosa pines). The oxygenated monoterpenes such as camphor, bornyl acetate, and cineole often compose high percentages of the monoterpenes within plant tissues, but are much less abundant in emission samples. Even after adjusting for lower vapor pressures of these compounds, emission rates relative to the hydrocarbon monoterpenes are often lower than would be expected from their internal concentrations. More study is warranted on monoterpene emission rates and composition, especially from the spruces, true firs, hemlocks, cedars, and some deciduous species such as the maples. Non-invasive canopy level and whole ecosystem flux studies are also needed to establish uncertainty estimates for monoterpene emission models. © 2000 Elsevier Science Ltd. All rights reserved

Biogenic isoprene emission: Model evaluation in a southeastern United States bottomland deciduous forest

Isoprene is usually the dominant natural volatile organic compound emission from forest ecosystems, especially those with a major broadleaf deciduous component. Here we report isoprene emission model performance versus leaf and canopy level isoprene emission measurements made at the Duke University Research Forest near Chapel Hill, North Carolina. Emission factors, light and temperature response, canopy environment models, foliar mass, leaf area, and canopy level isoprene emission were evaluated in the field and compared with model estimates. Model components performed reasonably well and generally yielded estimates within 20% of values measured at the site. However, measured emission factors were much higher in early summer following an unusually dry spring. These decreased later in the summer but remained higher than values currently used in emission models. There was also a pronounced decline in basal emission rates in lower portions of the canopy which could not be entirely explained by decreasing specific leaf weight. Foliar biomass estimates by genera using basal area ratios adjusted for crown form were in excellent agreement with values measured by litterfall. Overall, the stand level isoprene emissions determined by relaxed eddy accumulation techniques agreed reasonably well with those predicted by the model, although there is some evidence for underprediction at ambient temperatures approaching 30°C, and overprediction during October as the canopy foliage senesced. A "Big Leaf" model considers the canopy as a single multispecies layer and expresses isoprene emission as a function of leaf area rather than mass. This simple model performs nearly as well as the other biomass-based models. We speculate that seasonal water balance may impact isoprene emission. Possible improvements to the canopy environment model and other components are discussed

Performance test of a sorbent tube sampler with respect to analyte loss in collecting biogenic volatile organic compounds

The superiority of thermal desorption-gas chromatography (TD-GC) applications is well known for the analysis of biogenic volatile organic compounds (BVOC). Despite the recognition of potential biases associated with sorptive loss reaction, the interaction of reactive BVOC with a sorbent tube (ST) sampler has not been sufficiently investigated. In this study, the extent of such a loss on a sampling device was studied against the sorbent holder materials by comparing stainless steel (SS; main target) and quartz (QZ; reference). To this end, three bed STs (Tenax TA, Carbopack B, and Carbopack X) were prepared using both holding materials (SS vs. QZ). The extent of BVOC loss was then tested for each material against two different phases (liquid and vapor) of ten monoterpenes. Accordingly, the soptive loss on the SS holder ranged from 10 % (vapor) to 20 % (liquid). If a vapor phase BVOC was forced to pass through an empty SS tube, the extent of their loss increased further in a range of 21.1 % (β-P) to 43.5 % (α-T). Likewise, similar loss rates (about 10 % reductions) were also observed when analyzing some environmental samples (pine needle) from the SS holder relative to QZ. Thus, a QZ tube is recommended over a SS tube to avoid sample loss in the collection of BVOC.This research was supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Science, ICT and Future Planning (grant number 2013004624). We also acknowledges the support of “Cooperative Research Program for Agriculture Science & Technology Development (Project title: Study on model development to control odor from Pigpen Project No. PJ01052101)” Rural Development Administration, Republic of Korea