1,891 research outputs found

    Canopy uptake dominates nighttime carbonyl sulfide fluxes in a boreal forest

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    Nighttime vegetative uptake of carbonyl sulfide (COS) can exist due to the incomplete closure of stomata and the light independence of the enzyme carbonic anhydrase, which complicates the use of COS as a tracer for gross primary productivity (GPP). In this study we derived nighttime COS fluxes in a boreal forest (the SMEAR II station in Hyytiälä, Finland; 61°51′ N, 24°17′ E; 181 m a.s.l.) from June to November 2015 using two different methods: eddy-covariance (EC) measurements (FCOS-EC) and the radon-tracer method (FCOS-Rn). The total nighttime COS fluxes averaged over the whole measurement period were −6.8 ± 2.2 and −7.9 ± 3.8 pmol m−2 s−1 for FCOS-Rn and FCOS-EC, respectively, which is 33–38 % of the average daytime fluxes and 21 % of the total daily COS uptake. The correlation of 222Rn (of which the source is the soil) with COS (average R2  =  0.58) was lower than with CO2 (0.70), suggesting that the main sink of COS is not located at the ground. These observations are supported by soil chamber measurements that show that soil contributes to only 34–40 % of the total nighttime COS uptake. We found a decrease in COS uptake with decreasing nighttime stomatal conductance and increasing vapor-pressure deficit and air temperature, driven by stomatal closure in response to a warm and dry period in August. We also discuss the effect that canopy layer mixing can have on the radon-tracer method and the sensitivity of (FCOS-EC) to atmospheric turbulence. Our results suggest that the nighttime uptake of COS is mainly driven by the tree foliage and is significant in a boreal forest, such that it needs to be taken into account when using COS as a tracer for GPP

    Evaluating two soil carbon models within the global land surface model JSBACH using surface and spaceborne observations of atmospheric CO<sub>2</sub>

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    The trajectories of soil carbon (C) in the changing climate are of utmost importance, as soil carbon is a substantial carbon storage with a large potential to impact the atmospheric carbon dioxide (CO2) burden. Atmospheric CO2 observations integrate all processes affecting C exchange between the surface and the atmosphere. Therefore they provide a benchmark for carbon cycle models. We evaluated two distinct soil carbon models (CBALANCE and YASSO) that were implemented to a global land surface model (JSBACH) against atmospheric CO2 observations. We transported the biospheric carbon fluxes obtained by JSBACH using the atmospheric transport model TM5 to obtain atmospheric CO2. We then compared these results with surface observations from Global Atmosphere Watch (GAW) stations as well as with column XCO2 retrievals from the GOSAT satellite. The seasonal cycles of atmospheric CO2 estimated by the two different soil models differed. The estimates from the CBALANCE soil model were more in line with the surface observations at low latitudes (0 N–45 N) with only 1 % bias in the seasonal cycle amplitude (SCA), whereas YASSO was underestimating the SCA in this region by 32 %. YASSO gave more realistic seasonal cycle amplitudes of CO2 at northern boreal sites (north of 45 N) with underestimation of 15 % compared to 30 % overestimation by CBALANCE. Generally, the estimates from CBALANCE were more successful in capturing the seasonal patterns and seasonal cycle amplitudes of atmospheric CO2 even though it overestimated soil carbon stocks by 225 % (compared to underestimation of 36 % by YASSO) and its predictions of the global distribution of soil carbon stocks was unrealistic. The reasons for these differences in the results are related to the different environmental drivers and their functional dependencies of these two soil carbon models. In the tropical region the YASSO model showed earlier increase in season of the heterotophic respiration since it is driven by precipitation instead of soil moisture as CBALANCE. In the temperate and boreal region the role of temperature is more dominant. There the heterotophic respiration from the YASSO model had larger annual variability, driven by air temperature, compared to the CBALANCE which is driven by soil temperature. The results underline the importance of using sub-yearly data in the development of soil carbon models when they are used in shorter than annual time scales

    The thermal state of molecular clouds in the Galactic Center: evidence for non-photon-driven heating

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    We used the Atacama Pathfinder Experiment (APEX) 12 m telescope to observe the J_KaKc=3_03-2_02, 3_22-2_21, and 3_21-2_20 transitions of para-H_2CO at 218 GHz simultaneously to determine kinetic temperatures of the dense gas in the central molecular zone (CMZ) of our Galaxy. The map extends over approximately 40 arcmin x 8 arcmin (~100x20 pc^2) along the Galactic plane with a linear resolution of 1.2 pc. The strongest of the three lines, the H_2CO (3_03-2_02) transition, is found to be widespread, and its emission shows a spatial distribution similar to ammonia. The relative abundance of para-H_2CO is 0.5-1.2 10^{-9}, which is consistent with results from lower frequency H_2CO absorption lines. Derived gas kinetic temperatures for individual molecular clouds range from 50 K to values in excess of 100 K. While a systematic trend toward (decreasing) kinetic temperature versus (increasing) angular distance from the Galactic center (GC) is not found, the clouds with highest temperature (T_kin > 100 K) are all located near the nucleus. For the molecular gas outside the dense clouds, the average kinetic temperature is 65+/-10 K. The high temperatures of molecular clouds on large scales in the GC region may be driven by turbulent energy dissipation and/or cosmic-rays instead of photons. Such a non-photon-driven thermal state of the molecular gas provides an excellent template for the more distant vigorous starbursts found in ultraluminous infrared galaxies (ULIRGs).Comment: 23 pages, 11 figures, A&A in pres

    13CO(J=10)^{13}CO(J = 1 -- 0) Depression in Luminous Starburst Mergers

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    It is known that the class of luminous starburst galaxies tends to have higher R=12CO(J=10)/13CO(J=10)R =^{12}CO(J=1--0)/^{13}CO(J=1--0) integrated line intensity ratios (R>20R>20) than normal spiral galaxies (R10R \sim 10). Since most previous studies investigated only RR, it remains uncertain whether the luminous starburst galaxies are overabundant in 12^{12}CO or underabundant in 13^{13}CO. Here we propose a new observational test to examine this problem. Our new test is to compare far-infrared luminosities [LL(FIR)] with those of 12^{12}CO and 13CO[L(12CO)^{13}CO [L(^{12}CO) and L(13CO)L(^{13}CO), respectively]. It is shown that there is a very tight correlation between L(12CO)L(^{12}CO) and L(FIR), as found in many previous studies. However, we find that the 13^{13}CO luminosities of the high-R galaxies are lower by a factor of three on the average than those expected from the correlation for the remaining galaxies with ordinary RR values. Therefore, we conclude that the observed high RR values for the luminous starburst galaxies are attributed to their lower 13^{13}CO line intensities.Comment: 9 pages (aaspp4.sty), 3 postscript figures (embedded). Accepted for publication in Astrophysical Journal Letter

    Urban aerosol number size distributions

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    International audienceAerosol number size distributions were measured continuously in Helsinki, Finland from 5 May 1997 to 28 February 2003. The daily, monthly and annual patterns were investigated. The temporal variation of the particle number concentration was seen to follow the traffic density. The highest total particle number concentrations were usually observed during workdays; especially on Fridays, and the lower concentrations occurred during weekends; especially Sundays. Seasonally, the highest total number concentrations were usually observed during winter and spring and the lowest during June and July. More than 80\% of the particle number size distributions were tri-modal: nucleation mode (Dp 90 nm). Less than 20% of the particle number size distributions have either two modes or consisted of more than three modes. Two different measurement sites are used; in the first place (Siltavuori, 5 May 1997?5 March 2001), the overall means of the integrated particle number concentrations were 7100 cm?3, 6320 cm?3, and 960 cm?3, respectively, for nucleation, Aitken, and accumulation modes. In the second site (Kumpula, 6 March 2001?28 February 2003) they were 5670 cm?3, 4050 cm?3, and 900 cm?3. The total number concentration in nucleation and Aitken modes were usually significantly higher during weekdays than during weekends. The variations in accumulation mode were less pronounced. The smaller concentrations in Kumpula were mainly due to building construction and also slight overall decreasing trend during these years. During the site changing a period of simultaneous measurements over two weeks were performed showing nice correlation in both sites

    On the disappearance of a cold molecular torus around the low-luminosity active galactic nucleus of NGC 1097

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    We used the Atacama Large Millimeter/submillimeter Array (ALMA) to map the CO(3-2) and the underlying continuum emissions around the type 1 low-luminosity active galactic nucleus (LLAGN; bolometric luminosity 1042\lesssim 10^{42} erg~s1^{-1}) of NGC 1097 at 10\sim 10 pc resolution. These observations revealed a detailed cold gas distribution within a 100\sim 100 pc of this LLAGN. In contrast to the luminous Seyfert galaxy NGC 1068, where a 7\sim 7 pc cold molecular torus was recently revealed, a distinctively dense and compact torus is missing in our CO(3-2) integrated intensity map of NGC 1097. Based on the CO(3-2) flux, the gas mass of the torus of NGC 1097 would be a factor of 23\gtrsim 2-3 less than that found for NGC 1068 by using the same CO-to-H2_2 conversion factor, which implies less active nuclear star formation and/or inflows in NGC 1097. Our dynamical modeling of the CO(3-2) velocity field implies that the cold molecular gas is concentrated in a thin layer as compared to the hot gas traced by the 2.12 μ\mum H2_2 emission in and around the torus. Furthermore, we suggest that NGC 1097 hosts a geometrically thinner torus than NGC 1068. Although the physical origin of the torus thickness remains unclear, our observations support a theoretical prediction that geometrically thick tori with high opacity will become deficient as AGNs evolve from luminous Seyferts to LLAGNs.Comment: 9 pages, 5 figures. Accepted for publication in ApJ

    Production, growth and properties of ultrafine atmospheric aerosol particles in an urban environment

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    Number concentrations of atmospheric aerosol particles were measured by a flow-switching type differential mobility particle sizer in an electrical mobility diameter range of 6–1000 nm in 30 channels near central Budapest with a time resolution of 10 min continuously from 3 November 2008 to 2 November 2009. Daily median number concentrations of particles varied from 3.8 &amp;times; 10&lt;sup&gt;3&lt;/sup&gt; to 29 &amp;times;10&lt;sup&gt;3&lt;/sup&gt; cm&lt;sup&gt;−3&lt;/sup&gt; with a yearly median of 11.8 &amp;times; 10&lt;sup&gt;3&lt;/sup&gt; cm&lt;sup&gt;−3&lt;/sup&gt;. Contribution of ultrafine particles to the total particle number ranged from 58 to 92% with a mean ratio and standard deviation of (79 &amp;plusmn; 6)%. Typical diurnal variation of the particle number concentration was related to the major emission patterns in cities, new particle formation, sinks of particles and meteorology. Shapes of the monthly mean number size distributions were similar to each other. Overall mean for the number median mobility diameter of the Aitken and accumulation modes were 26 and 93 nm, respectively, which are substantially smaller than for rural or background environments. The Aitken and accumulation modes contributed similarly to the total particle number concentrations at the actual measurement location. New particle formation and growth unambiguously occurred on 83 days, which represent 27% of all relevant days. Hence, new particle formation and growth are not rare phenomena in Budapest. Their frequency showed an apparent seasonal variation with a minimum of 7.3% in winter and a maximum of 44% in spring. New particle formation events were linked to increased gas-phase H&lt;sub&gt;2&lt;/sub&gt;SO&lt;sub&gt;4&lt;/sub&gt; concentrations. In the studied area, new particle formation is mainly affected by condensation sink and solar radiation. The formation process seems to be not sensitive to SO&lt;sub&gt;2&lt;/sub&gt;, which was present in a yearly median concentration of 6.7 μg m&lt;sup&gt;−3&lt;/sup&gt;. This suggests that the precursor gas was always available in excess. Formation rate of particles with a diameter of 6 nm varied between 1.65 and 12.5 cm&lt;sup&gt;−3&lt;/sup&gt; s&lt;sup&gt;−1&lt;/sup&gt; with a mean and standard deviation of (4.2 &amp;plusmn; 2.5) cm&lt;sup&gt;−3&lt;/sup&gt; s&lt;sup&gt;−1&lt;/sup&gt;. Seasonal dependency for the formation rate could not be identified. Growth curves of nucleated particles were usually superimposed on the characteristic diurnal pattern of road traffic direct emissions. The growth rate of the nucleation mode with a median diameter of 6 nm varied from 2.0 to 13.3 nm h&lt;sup&gt;−1&lt;/sup&gt; with a mean and standard deviation of (7.7 &amp;plusmn; 2.4) nm h&lt;sup&gt;−1&lt;/sup&gt;. There was an indicative tendency for larger growth rates in summer and for smaller values in winter. New particle formation events increased the total number concentration by a mean factor and standard deviation of 2.3 &amp;plusmn; 1.1 relative to the concentration that occurred immediately before the event. Several indirect evidences suggest that the new particle formation events occurred at least over the whole city, and were of regional type. The results and conclusions presented are the first information of this kind for the region over one-year long time period

    Onset of photosynthesis in spring speeds up monoterpene synthesis and leads to emission bursts

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    Emissions of biogenic volatile organic compounds (BVOC) by boreal evergreen trees have strong seasonality, with low emission rates during photosynthetically inactive winter and increasing rates towards summer. Yet, the regulation of this seasonality remains unclear. We measured in situ monoterpene emissions from Scots pine shoots during several spring periods and analysed their dynamics in connection with the spring recovery of photosynthesis. We found high emission peaks caused by enhanced monoterpene synthesis consistently during every spring period (monoterpene emission bursts, MEB). The timing of the MEBs varied relatively little between the spring periods. The timing of the MEBs showed good agreement with the photosynthetic spring recovery, which was studied with simultaneous measurements of chlorophyll fluorescence, CO2 exchange and a simple, temperature history-based proxy for state of photosynthetic acclimation, S. We conclude that the MEBs were related to the early stages of photosynthetic recovery, when the efficiency of photosynthetic carbon reactions is still low whereas the light harvesting machinery actively absorbs light energy. This suggests that the MEBs may serve a protective functional role for the foliage during this critical transitory state and that these high emission peaks may contribute to atmospheric chemistry in the boreal forest in springtime. Emissions of biogenic volatile organic compounds (BVOC) by boreal evergreen trees have strong seasonality. We measured high emission peaks from Scots pine shoots caused by enhanced monoterpene synthesis taking place simultaneously with the photosynthetic spring recovery. We conclude that the increased emissions were related to the photosynthetic recovery, when the efficiency of photosynthetic carbon reactions is low whereas the light harvesting machinery actively absorbs light energy. Increased emissions may serve a protective functional role for the foliage during the transitory state, and these high emission peaks may contribute to atmospheric chemistry in the boreal forest in springtime.Peer reviewe

    The Central Region of Barred Galaxies: Molecular Environment, Starbursts, and Secular Evolution

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    Despite compelling evidence that stellar bars drive gas into the inner 1--2 kpc or circumnuclear (CN) region of galaxies, there are few large, high resolution studies of the CN molecular gas and star formation (SF). We study a sample of local barred non-starbursts and starbursts with high-resolution CO, optical, Ha, RC, Br-gamma, and HST data, and find the following. (1) The inner kpc of bars differs markedly the outer disk and hosts molecular gas surface densities Sigma-gas-m of 500-3500 Msun pc-2, gas mass fractions of 10--30 %, and epicyclic frequencies of several 100--1000 km s-1 kpc-1.Consequently, gravitational instabilities can only set in at high gas densities and grow on a short timescale (few Myr). This high density, short timescale, `burst' mode may explain why powerful starbursts tend to be in the CN region of galaxies. (2) We suggest that the variety in CO morphologies is due to different stages of bar-driven inflow. At late stages, most of the CN gas is inside the outer inner Lindblad resonance (OILR), and has predominantly circular motions. Across the sample, we find bar pattern speeds with upper limits of 43 to 115 km s-1 kpc-1 and OILR radii of > 500 pc. (3) Barred starbursts and non-starbursts have CN SFRs of 3--11 and 0.1--2 Msun yr-1, despite similar CN gas mass. Sigma-gas-m in the starbursts is larger (1000--3500 Msun pc-2) and close to the Toomre critical density over a large region. (4) Molecular gas makes up 10%--30% of the CN dynamical mass (6--30 x 10^9 Msun).In the starbursts, it fuels CN SFRs of 3--11 Msun yr-1, building young, massive, high V/sigma components. We present evidence for such a pseudo-bulge in NGC 3351. Implications for secular evolution along the Hubble sequence are discussed.Comment: Accepted by the Astrophysical Journal. Paper length reduced to fit within APJ page limits. Version of paper with high resolution figures is at http://www.as.utexas.edu/~sj/papers/ms-hires-sj05a.ps.g

    The analysis of size-segregated cloud condensation nuclei counter (CCNC) data and its implications for cloud droplet activation

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    Ambient aerosol, CCN (cloud condensation nuclei) and hygroscopic properties were measured with a size-segregated CCNC (cloud condensation nuclei counter) in a boreal environment of southern Finland at the SMEAR (Station for Measuring Ecosystem-Atmosphere Relations) II station. The instrumental setup operated at five levels of supersaturation <i>S</i> covering a range from 0.1–1% and measured particles with a size range of 20–300 nm; a total of 29 non-consecutive months of data are presented. The median critical diameter <i>D</i><sub>c</sub> ranged from 150 nm at <i>S</i> of 0.1% to 46 nm at <i>S</i> of 1.0%. The median aerosol hygroscopicity parameter &kappa; ranged from 0.41 at <i>S</i> of 0.1% to 0.14 at <i>S</i> of 1.0%, indicating that ambient aerosol in Hyytiälä is less hygroscopic than the global continental or European continental averages. It is, however, more hygroscopic than the ambient aerosol in an Amazon rainforest, a European high Alpine site or a forested mountainous site. A fairly low hygroscopicity in Hyytiälä is likely a result of a large organic fraction present in the aerosol mass comparative to other locations within Europe. A considerable difference in particle hygroscopicity was found between particles smaller and larger than ~100 nm in diameter, possibly pointing out to the effect of cloud processing increasing &kappa; of particles > 100 nm in diameter. The hygroscopicity of the smaller, ~50 nm particles did not change seasonally, whereas particles with a diameter of ~150 nm showed a decreased hygroscopicity in the summer, likely resulting from the increased VOC emissions of the surrounding boreal forest and secondary organic aerosol (SOA) formation. For the most part, no diurnal patterns of aerosol hygroscopic properties were found. Exceptions to this were the weak diurnal patterns of small, ~50 nm particles in the spring and summer, when a peak in hygroscopicity around noon was observed. No difference in CCN activation and hygroscopic properties was found on days with or without atmospheric new particle formation. During all seasons, except summer, a CCN-inactive fraction was found to be present, rendering the aerosol of 75–300 nm in diameter as internally mixed in the summer and not internally mixed for the rest of the year
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