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1.
Atmospheric oxidation of monoterpenes contributes to formation of tropospheric ozone and secondary organic aerosol, but their products are poorly characterized. In this work, we report a series of outdoor smog chamber experiments to investigate both gaseous and particulate products in the ozone oxidation of four monoterpenes: -pinene, -pinene, 3-carene, and sabinene. More than ten oxygenated products are detected and identified in each monoterpene/O3 reaction by coupling derivatization techniques and GC/MS detection. A denuder/filter pack sampling system is used to separate and simultaneously collect gas and aerosol samples. The identified products, consisting of compounds containing carbonyl, hydroxyl, and carboxyl functional groups, are estimated to account for about 34–50%, 57%, 29–67%, and 24% of the reacted carbon mass for -pinene, sabinene, -pinene, and 3-carene, respectively. The identified individual products account for >83%, 100%, >90%, and 61% of the aerosol mass produced in the ozone reaction of -pinene, sabinene, -pinene, and 3-carene. The uncertainty in the yield data is estimated to be ±50%. Many of the products partition between gas and aerosol phases, and their gas-aerosol partitioning coefficients are determined and reported here. Reaction schemes are suggested to account for the products observed.  相似文献   

2.
Stable Isotope Ratios: Hurricane Olivia   总被引：1，自引：0，他引：1  
The oxygen and hydrogen isotopic compositions of rains from HurricaneOlivia (1994) in the eastern Pacific were measured. The rains werecollected on 24 and 25 September during airplane flights conducted at anelevation of 3 km. Hurricane Olivia peaked in intensity to a category-4storm between the two dates. Isotope ratios of rains from HurricaneOlivia were markedly lower ( 18O = –13.9to –28.8) than that of rain collected from a thunderstormat an elevation of 2.3 km outside the influence of Olivia (18O = –3.8). A distinct decrease in isotoperatios from the first day to the next ( 18O =–18.4 to –21.9) in Hurricane Olivia wasattributed to decreased updraft velocities and outflow aloft. Thisshifted the isotopic water mass balance so that fewer hydrometeors werelifted and more ice descended to flight level. A decrease in the averagedeuterium excess from the first day to the next (d = 15.5 to 7.1)was attributed to an increase in the relative humidity of the watervapor `source' area. We hypothesize that the `source' region for therain was in the boundary layer near the storm center and that becausethe hurricane was at peak intensity prior to the second day the relative humidity was higher.  相似文献   

3.
Summary The influence of agricultural management on the CO2 budget of a typical subalpine grassland was investigated at the Swiss CARBOMONT site at Rigi-Seebodenalp (1025m a.s.l.) in Central Switzerland. Eddy covariance flux measurements obtained during the first growing season from the mid of spring until the first snow fall (17 Mai to 25 September 2002) are reported. With respect to the 10-year average 1992–2001, we found that this growing season had started 10 days earlier than normal, but was close to average temperature with above-normal precipitation (100–255% depending on month). Using a footprint model we found that a simple approach using wind direction sectors was adequate to classify our CO2 fluxes as being controlled by either meadow or pasture. Two significantly different light response curves could be determined: one for periods with external interventions (grass cutting, cattle grazing) and the other for periods without external interventions. Other than this, meadow and pasture were similar, with a net carbon gain of –128±17g Cm–2 on the undisturbed meadow, and a net carbon loss of 79±17g Cm–2 on the managed meadow, and 270±24g Cm–2 on the pasture during 131 days of the growing season, respectively. The grass cut in June reduced the gross CO2 uptake of the meadow by 50±2% until regrowth of the vegetation. Cattle grazing reduced gross uptake over the whole vegetation period (37±2%), but left respiration at a similar level as observed in the meadow.  相似文献   

4.
Summary The evolving modes of the sea-surface temperature (SST) in the Tropical Atlantic on the short interannual (IA) timescale were obtained by performing the extended empirical orthogonal function (EEOF) analyses on this variable separately for the 106-year (1871–1976) and 20-year (1881–1900; 1901–1920; 1921–1940; 1941–1960) periods. The equatorial and inter-hemispheric patterns manifest in the first EEOF mode of each analysis as part of the short IA evolution of the SST anomalies in the Tropical Atlantic. Another outstanding feature of the first EEOF mode of each analysis concerns the propagations of the SST anomalies in the meridional direction within the 20°N–20°S band and in the zonal direction in the sector 40°W–20°W. For all analyses, the SST anomalies propagate northward from the equator to 15°N and southward from 20°N to 15°N, with the same sign anomalies merging approximately at 15°N. On the other hand, the SST anomalies propagate westward in the sector 40°W–20°W with a propagation rate close to that of the phase speed of the fastest baroclinic Rossby wave in the ocean. So, the observed propagations of the SST anomalies in the 20°N–20°S band might result from the combined effect of the surface oceanic currents in this band and the baroclinic Rossby waves in the ocean.  相似文献   

5.
In this paper we analyse diabatic wind profiles observed at the 213 m meteorological tower at Cabauw, the Netherlands. It is shown that the wind speed profiles agree with the well-known similarity functions of the atmospheric surface layer, when we substitute an effective roughness length. For very unstable conditions, the agreement is good up to at least 200 m or z/L–7(z is height, L is Obukhov length scale). For stable conditions, the agreement is good up to z/L1. For stronger stability, a semi-empirical extension is given of the log-linear profile, which gives acceptable estimates up to ~ 100 m. A scheme is used for the derivation of the Obukhov length scale from single wind speed, total cloud cover and air temperature. With the latter scheme and the similarity functions, wind speed profiles can be estimated from near-surface weather data only. The results for wind speed depend on height and stability. Up to 80 m, the rms difference with observations is on average 1.1 m s–1. At 200 m, 0.8 m s–1 for very unstable conditions increasing to 2.1 m s–1 for very stable conditions. The proposed methods simulate the diurnal variation of the 80 m wind speed very well. Also the simulated frequency distribution of the 80 m wind speed agrees well with the observed one. It is concluded that the proposed methods are applicable up to at least 100 m in generally level terrain.  相似文献   

6.
From measurements in the atmospheric surface layer over a paddy field, the Kolmogorov constants for CO2 and longitudinal wind velocity were obtained. In this study, the nondimensional dissipation rate nc = (1–16 v )-1/2 for CO2 variance and = (1–16 v )-1/4 – v for turbulent energy were used, assuming the equality of the local production term and the local dissipation term, and neglecting the divergence flux term in the budget equation. The value of the constant for CO2 was consistent with recent determinations for temperature and humidity. The constant for longitudinal wind velocity showed good agreement with other recent observations.  相似文献   

7.
Aerosol chemical composition and trace gas measurements were made at twolocations on the northeastern peninsula of Tenerife during the ACE-2HILLCLOUD experiment, between 28 June and 23 July 1997. Measurementswere made of coarse (#gt;2.5 m aerodynamic diameter) and fine (#lt; 2.5m) aerosol Cl–, NO3 –,SO4 2–, non-sea saltSO4 2– (NSSS),CH3SO3 – (MSA) andNH4 +, and gas phase dimethylsulphide (DMS), HCl,HNO3, SO2, CH3COOH, HCOOH andNH3. Size distributions were measured using a cascadeimpactor. Results show that in marine air masses NSSS and MSA wereformed via DMS oxidation, with additional NSSS present in air massescontaining a continental component. Using a Eulerian box model approachfor aerosols transported between upwind and downwind sites, a mean NSSSproduction rate of 4.36 × 10–4 gm–3 s–1 was calculated for daytimeclear sky periods (highest insolation), with values for cloudy periodsduring daytime and nighttime of 3.55 × 10–4 and2.40 × 10–4 g m–3s–1, respectively. The corresponding rates for MSA were6.23 × 10–6, 8.49 × 10–6and 6.95 × 10–6 g m–3s–1, respectively. Molar concentration ratios forMSA/NSSS were 8.7% (1.8–18.2%) and 1.9%(1.3–3.5%) in clean and polluted air masses, respectively.Reactions occurring within clouds appeared to have a greater influenceon rates of MSA production, than of NSSS, while conversely daytime gasphase reactions were more important for NSSS. For MSA, nighttimein-cloud oxidation rates exceeded rates of daytime gas phase productionvia OH oxidation of DMS. NSSS, MSA and ammonium had trimodal sizedistributions, with modes at 0.3, 4.0 and >10.0 m (NSSS andNH4 +), and 0.3, 1.5 and 4.0 m (MSA). Nosignificant production of other aerosol species was observed, with theexception of ammonium, which was formed at variable rates dependent onneutralisation of the aerosol with ammonia released from spatiallynon-uniform surface sources. Seasalt components were mainly present incoarse particles, although sub-micrometre chloride was also measured.Losses by deposition exceeded calculated expectations for all species,and were highest for the seasalt fraction and nitrate.  相似文献   

8.
The design and performance of a smog chamber for the study of photochemical reactions under simulated environmental conditions is described. The chamber is thermostated for aerosol experiments, and it comprises a gas chromatographic sample enrichment system suitable for monitoring hydrocarbons at the ppbv level. By irradiating NO x /alkane-mixtures rate constants for the reaction of OH radicals with n-alkanes are determined from n-pentane to n-hexadecane to be (k±2)/10–12 cm3 s–1=4.29±0.16, 6.2±0.6, 7.52 (reference value), 8.8±0.3, 10.2±0.3, 11.7±0.4, 13.7±0.3, 15.1±0.5, 17.5±0.6, 19.3±0.7, 22.3±1.0, and 25.0±1.3, respectively at 312 K. Rate constants, (k±2)/10–17 cm3 s–1, for the reaction of ozone with trans-2-butene (21.2±1.0), cis-3-methylpentene-(2) (47.2±1.7), cyclopentene (62.4±3.5), cyclohexene (7.8±0.5), cycloheptene (28.3±1.5), -pinene (8.6±1.3), and -pinene (1.4±0.2) are determined in the dark at 297 K using cis-2-butene (13.0) as reference standard.  相似文献   

9.
Investigations were carried out as to the feasibility of using a semiconductor source in the design of a new rapid response, open-path hygrometer. A single-beam instrument was constructed employing an infrared light emitting diode (LED) as a source instead of the usual high energy, wideband filament. The spectral emission envelope encompassed the 1.87 m water absorption band. Electronic modulation and thermoelectrical cooling of the diode eliminated the conventional chopper wheel and stabilized the peak wavelength emission. Path length was 200 mm. Over a water vapour concentration range of 0–16 g m–3, absorption varied by 2% in a linear fashion. At 10 Hz, the noise level was 0.1 g m–3 rms. Hygrometer resolution and stability are constrained by the detector noise level, the small source emission in the absorption band and low frequency drift in the optical filter. Despite these problems, the new instrument showed comparable performance characteristics to a commercial Lyman- hygrometer. Latent heat fluxes measured with both instruments and a Kaijo-Denki, 3-D sonic anemometer agreed to within 4% over a range 0–350 W m–2. Further improvements in performance can be anticipated with advances in detector and LED technology.  相似文献   

10.
We present the first application of a multi-stage impactor to study volcanic particle emissions to the troposphere from Masaya volcano, Nicaragua. Concentrations of soluble SO4 2–,Cl–, F–, NO3 –, K+, Na+,NH4 +, Ca2+ and Mg2+ were determined in 11 size bins from 0.07 m to >25.5 m. The near-source size distributions showed major modes at 0.5m (SO4 2–, H+,NH4 +); 0.2 m and 5.0 m (Cl–) and 2.0–5.0 m(F–). K+ and Na+ mirrored the SO4 2– size-resolvedconcentrations closely, suggesting that these were transported primarily asK2SO4 and Na2SO4 in acidic solution, while Mg2+ andCa2+ presented modes in both <1 m and >1 m particles. Changes in relative humidity were studied by comparing daytime (transparent plume) and night-time (condensed plume) results. Enhanced particle growth rates were observed in the night-time plume as well as preferential scavenging of soluble gases, such as HCl, by condensed water. Neutralisation of the acidic aerosol by background ammonia was observed at the crater rim and to a greater extent approximately 15 km downwind of the active crater. We report measurements of re-suspended near-source volcanic dust, which may form a component of the plume downwind. Elevated levels ofSO4 2–, Cl–, F–,H+, Na+, K+ and Mg2+ were observed around the 10 m particle diameter in this dust. The volcanic SO4 2– flux leaving the craterwas 0.07 kg s–1.  相似文献   

11.
The budget equation for carbon dioxide variance can be represented by production, dissipation and flux divergence terms. Each term is measured under near neutral to moderately unstable conditions over vegetated fields. The flux divergence term is about an order of magnitude smaller than production and dissipation terms, though it shows a loss for 0.006 < v < 1 and a gain for 1 < - v < 10. Here, v is the Monin-Obukhov stability parameter including humidity effect. As expected from a closure of the budget, the nondimensional production and dissipation terms are basically identical and represented by the same functional form: (1–16 v )–1/2.  相似文献   

12.
A technique was developed that allows the determination of the stable carbon isotope ratio of isoprene in air. The method was used for a limited number of ambient measurements as well as laboratory studies of isoprene emitted from Velvet Bean (Mucana pruriens L. var. utilis), including the light and temperature dependence. The mean stable carbon isotope ratio ( 13C) of isoprene emitted from Velvet Bean (Mucana pruriens L. var. utilis) for all our measurements is –27.7 ± 2.0 (standard deviation for 23 data points). Our results indicate a small dependence of the stable carbon isotope ratios on leaf temperature and photosynthetic photon flux density (PPFD). The light dependence is 0.0026 ± 0.0012/( mol of photons m–2 s–1) for the studied range from 400 to 1700 mol of photons m–2 s–1. The temperature dependence is 0.16 ± 0.09/K. On average, the emitted isoprene is 2.6 ± 0.9 lighter than the leaf carbon. An uncertainty analysis of the possibility to use stable carbon isotope ratio measurements of isoprene for estimates of its mean photochemical age suggests that meaningful results can be obtained. This is supported by the results of a small number of measurements of the stable carbon isotope composition of ambient isoprene at different locations. The results range from approximately –29 to –16. They are consistent with vegetation emissions of isoprene that is slightly depleted in 13C relative to the plant material and enrichment of 13C in the atmosphere due to isotope fractionation associated with the reaction with OH-radicals. The stable carbon isotope ratio of ambient isoprene at locations directly influenced by isoprene emissions is very close to the values we found in our emission studies, whereas at sites located remote from isoprene emitting vegetation we find substantial enrichment of 13C. This suggests that stable carbon isotope ratio measurements will be a valuable, quantitative method to determine the extent of photochemical processing of isoprene in ambient air.  相似文献   

13.
Weekly bulk aerosol samples collected at Funafuti, Tuvalu (8°30S, 179°12E), American Samoa (14°15S, 170°35W), and Rarotonga (21°15S, 159°45W), from 1983 through most of 1987 have been analyzed for nitrate and other constituents. The mean nitrate concentration is about 0.11 g m–3 at each of these stations: 0.107±0.011 g m–3 at Funafuti; 0.116±0.008 at American Samoa; and 0.117±0.010 at Rarotonga. Previous measurements of mineral aerosol and trace metal concentrations at American Samoa are among the lowest ever recorded for the near-surface troposphere and indicate that this region is minimally affected by transport of soil material and pollutants from the continents. Consequently, the nitrate concentration of 0.11 g m–3 can be regarded as the natural level for the remote marine boundary layer of the tropical South Pacific Ocean. In contrast, over the tropical North Pacific which is significantly impacted by the transport of material from Asia and North America, the mean nitrate concentrations are about three times higher, 0.29 and 0.36 g m–3 at Midway and Oahu, respectively. The major sources of the nitrate over the tropical South Pacific are still very uncertain. A very significant correlation between the nitrate concentrations at American Samoa and the concentrations of 210Pb suggests that transport from continental sources might be important. This continental source could be lightning, which occurs most frequently over the tropical continents. A near-zero correlation with 7Be indicates that the stratosphere and upper troposphere are probably not the major sources. A significant biogenic source would be consistent with the higher mean nitrate concentrations, 0.16 to 0.17 g m–3, found over the equatorial Pacific at Fanning Island (3°55N, 159°20W) and Nauru (0°32S, 166°57E). The lack of correlation between nitrate and nss sulfate at American Samoa does not necessarily preclude an important role for marine biogenic sources.  相似文献   

14.
The Petryanov air filters combined into half-year sets were analyzed for the presence of 40K, 137Cs and 22Na by means of low-background gamma rays spectrometry. Each sample contains aerosols from more than 1 Mm3 of air. Samples were collected in ground level air at Kraków (Southern Poland) from 1996 to 2002. Activity concentrations of 40K are almost constant with the mean of 14.7± 4.5 Bq m–3. Activity concentrations of 137Cs, which are on the level of single Bq m– 3 show exponential decrease with effective half-life time of 7.07± 0.77 years. The cosmogenic 22Na shows a strong seasonal variation with significant different mean values activity concentration between 0.333± 0.095 Bq m–3 and 0.137± 0.045 Bq m–3, for summer and winter, respectively. Moreover, the activity ratio for two cosmogenic radionuclides: 22Na and measured previously 7Be show also changes with statistically significant seasonal differences. The lower values were found during winters. The mechanisms which might govern this ratio are discussed. The conclusion is that transport of 22Na during summer seems to be so much effective, that results in kind of relative depletion of stratosphere of this nuclide.  相似文献   

15.
The stable carbon isotope ratios of nonmethane hydrocarbons (NMHC) and methyl chloride emitted from biomass burning were determined by analyzing seven whole air samples collected during different phases of the burning process as part of a laboratory study of wood burning. The average of the stable carbon isotope ratios of emitted alkanes, alkenes and aromatic compounds is identical to that of the burnt fuel; more than 50% of the values are within a range of ±1.5 of thecomposition of the burnt fuel wood. Thus for the majority of NMHC emitted from biomass burning stable carbon isotope ratio of the burnt fuel a good first order approximation for the isotopic composition of the emissions. Of the more than twenty compounds we studied, only methyl chloride and ethyne differed in stable carbon isotope ratios by more than a few per mil from the composition of the fuel. Ethyne is enriched in 13C by approximately 20–30, and most of the variability can beexplained by a dependence on flame temperature. The 13C values decreaseby 0.019 /K (±0.0053/K) with increasing temperature. Methyl chloride is highly depleted in 13C, on average by25. However the results cover a wide range of nearly 30. Specifically, in two measurements with wood from Eucalyptus (Eucalyptus delegatensis) as fuel we observed the emission of extremely light methyl chloride (–68.5and–65.5). This coincides with higher than average emission ratiosfor methyl chloride (15.5 × 10–5 and 18 ×10–5 mol CH3Cl/mol CO2). These high emission ratios are consistent with the highchlorine content of the burnt fuel, although, due to the limited number of measurements, it would be premature to generalize these findings. The limited number of observations also prevents any conclusion on a systematic dependence between chlorine content of the fuel, emission ratios and stable carbon isotope ratio of methyl chloride emissions. However, our results show that a detailed understanding of the emissions of methyl chloride from chloride rich fuels is important for understanding its global budget. It is also evident that the usefulness of stable carbon isotope ratios to constrain the global budget of methyl chloride will be complicated by the very large variability of the stable carbon isotope ratio of biomass burning emissions. Nevertheless, ultimately the large fractionation may provide additional constraints for the contribution of biomass burning emissions to the atmospheric budget of methyl chloride.  相似文献   

16.
The formation yields of nine carbonyl products are reported from the gas-phase OH radical-initiated reactions (in the presence of NO x ) and the O3 reactions with seven monoterpenes. The products were identified using GC/MS and GC-FTIR and quantified by GC-FID analyses of samples collected on Tenax solid adsorbent cartridges. The identities of products from camphene, limonene and -pinene were confirmed by comparison with authentic standards. Sufficient quantities of products from the 3-carene, limonene, -pinene, sabinene and terpinolene reactions were isolated to allow structural confirmation by proton NMR spectroscopy. The measured total carbonyl formation yields ranged from non-detectable for the OH radical reaction with camphene and the O3 reactions with 3-carene and limonene to 0.5 for the OH radical reaction with limonene and the O3 reaction with sabinene.  相似文献   

17.
Current inventories of terpenes released from vegetation consider only the short-term influences of light and temperature on emissions to simulate temporal variation during the year. We studied whole canopy emissions from young Pinus pinea during a 15-month enclosure in greenhouse chambers and examined data for other long-term influences. Mean daytime emission rates strongly increased during spring, reached an annual maximum of 200 pmol m–2 total needle area s–1 (1.1 g g–1 leaf dry weight h–1) between mid June and mid August, strongly declined in fall and reached an annual minimum of 1 pmol m–2 s–1 (0.006 g g–1 h–1) between January and February. Normalization to standard temperature and light conditions did not change the annual time course of emissions, but reduced summer to winter ratio from a factor of 200 to about 45. Seasonal variation was characterized also by changes in terpene composition: among the six main compounds, three (t--ocimene, linalool, 1.8-cineol) were exclusively emitted during sunlit hours in the main vegetation period, whereas the other (limonene, -pinene, myrcene) were emitted day and night and throughout the seasons. The results suggest that different terpene sources in P. pinea foliage exist and that a great part of the annual emission course observed here results from seasonal influences on these sources. A global model to simulate plant emissions is proposed, which accounts for seasonal influences on emissions in addition to the short-term effects of temperature and light. The model is tested on field data and discussed for its general application.  相似文献   

18.
The emission targets adopted in the Kyoto Protocol1 far exceed thelikely level of emissions from Russia and Ukraine. These countries could selltheir surplus if the Protocol is followedand industrialized countries establish an international emission tradingsystem. Critics have condemned the potentialsale and dubbed the surplus hot air because it does not represent anyreduction in emissions below the level thatwould have occurred anyway. Using the most recent, comprehensive regionalscenarios2 for the emissions of carbon dioxide from the energysystem, we estimate that during the Protocol's2008–2012 budget period the surplus will range from 9 MtC (milliontons of carbon) to 900 MtC for Russia andfrom 3 MtC to 200 MtC for Ukraine. Even scenarios with high economic growthand carbon-intensive technologies donot exhaust the surplus before the budget period. In the central (middlecourse) scenario, the total carbon surplusexceeds 1000 MtC and is worth 22 to 170 billion U.S. dollars (4 to 34 billionU.S. dollars per year). This flow ofrevenues, which could exceed Russian earnings from natural gas exports($10 billion in 19973), is comparable with the projectedtotal investmentsof the Russian energy system for 2008–2012. If directed towardslow-carbon infrastructure investments (e.g., gaspipelines), surplus transfers could reinforce and partially lock-indecarbonization of the world energy system.  相似文献   

19.
Measurements have been made with fast-response multi-channel temperature, humidity and refractive index sensors flown to 2000 m on a tethered balloon to investigate small-scale fluctuations important in radio-wave scattering, their relation to atmospheric parameters, and their spatial variation in both one and three dimensions. Data from the three types of sensors at one point were consistent for frequencies up to about 8 Hz. Power spectra of data at various heights were computed over 0.1 to 10 Hz and generally showed slopes (on a log-log plot) close to - 5/3 above 1 Hz but ranged from –1.5 to – 3.5 at lower frequencies; in this range (f < 1 Hz) slopes were close to – 5/3 for negative Richardson number (Ri), provided temperature gradients were steeper than –1.1 °C 100 m–1 and wind shears > 1.4 x 10–2 s–1 approx. Steeper slopes were generally associated with stable atmospheric conditions but no precise relation to the above parameters was found. Spectral density was a maximum for Ri –0.75.Cross-correlations of 0.5 were frequently observed between sensors 1 m apart in orthogonal directions; in the vertical, examples of negative correlation of vapour pressure were occasionally found over this spacing. Using four sensors spaced in line over 9 m, cross-spectrum phase calculations of drift speeds were found to be consistent with measured wind speeds. The ratio of identification distance (coherence=0.6) to scale size of irregularities ranged from 0.25 to 0.5 with no apparent relation to height or meteorological parameters.  相似文献   

20.
Diurnal and vertical ambient air measurements of the monoterpenes have been made in and above a Scots pine (Pinus sylvestris) forest of central Sweden, within the boreal northern coniferous biome. Sampling was done with Tenax TA, and analysis by GC and ion trap detection. Daytime mixing ratios were on the order of tenths of a ppbv from the forest floor to the top of the forest, and a factor of 2 or 3 lower above the forest. Mixing ratios at night were at the ppbv level, highest near the forest floor and the crown, and decreased with height above the forest. The highest total concentration observed was 8 ppbv inside the forest at 3 am (GMT). The average terpene composition was 3-carene 32%, -pinene 29%, limonene 18%, -pinene 10%, -phellandrene 7%, camphene 5%, and sabinene at less than 2%. The 3-carene/-pinene ratio varied with wind direction and speed, relative humidity, and wet/dry vegetation, but not with ozone or NO2 concentration, solar radiation, or temperature. Variations in the observed terpene composition at the sampling site are mainly caused by the influence of other vegetation in the vicinity of the site. It would seem that wet Scots pine emits more 3-carene relative to -pinene than does dry pine.  相似文献   

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