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  • 1
    Publication Date: 2016-07-02
    Description: Previous empirical work has shown that feedbacks between fire severity, soil organic layer thickness, tree recruitment, and forest growth are important factors controlling carbon accumulation after fire disturbance. However, current boreal forest models inadequately simulate this feedback. We address this deficiency by updating the ED2 model to include a dynamic feedback between soil organic layer thickness, tree recruitment, and forest growth. The model is validated against observations spanning monthly to centennial time scales and ranging from Alaska to Quebec. We then quantify differences in forest development after fire disturbance resulting from changes in soil organic layer accumulation, temperature, nitrogen availability, and atmospheric CO 2 . First, we find that ED2 accurately reproduces observations when a dynamic soil organic layer is included. Second, simulations indicate that the presence of a thick soil organic layer after a mild fire disturbance decreases decomposition and productivity. The combination of the biological and physical effects increases or decreases total ecosystem carbon depending on local conditions. Third, with a 4°C temperature increase, some forests transition from undergoing succession to needleleaf forests to recruiting multiple cohorts of broadleaf trees, decreasing total ecosystem carbon by ∼40% after 300 years. However, the presence of a thick soil organic layer due to a persistently mild fire regime can prevent this transition and mediate carbon losses even under warmer temperatures. Fourth, nitrogen availability regulates successional dynamics; broadleaf species are less competitive with needleleaf trees under low nitrogen regimes. Fifth, the boreal forest shows additional short-term capacity for carbon sequestration as atmospheric CO 2 increases. This article is protected by copyright. All rights reserved.
    Electronic ISSN: 1942-2466
    Topics: Geography , Geosciences
    Published by Wiley on behalf of American Geophysical Union (AGU).
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  • 2
    Publication Date: 2011-10-01
    Description: The stable isotope ratios of atmospheric CO(2) ((18)O/(16)O and (13)C/(12)C) have been monitored since 1977 to improve our understanding of the global carbon cycle, because biosphere-atmosphere exchange fluxes affect the different atomic masses in a measurable way. Interpreting the (18)O/(16)O variability has proved difficult, however, because oxygen isotopes in CO(2) are influenced by both the carbon cycle and the water cycle. Previous attention focused on the decreasing (18)O/(16)O ratio in the 1990s, observed by the global Cooperative Air Sampling Network of the US National Oceanic and Atmospheric Administration Earth System Research Laboratory. This decrease was attributed variously to a number of processes including an increase in Northern Hemisphere soil respiration; a global increase in C(4) crops at the expense of C(3) forests; and environmental conditions, such as atmospheric turbulence and solar radiation, that affect CO(2) exchange between leaves and the atmosphere. Here we present 30 years' worth of data on (18)O/(16)O in CO(2) from the Scripps Institution of Oceanography global flask network and show that the interannual variability is strongly related to the El Nino/Southern Oscillation. We suggest that the redistribution of moisture and rainfall in the tropics during an El Nino increases the (18)O/(16)O ratio of precipitation and plant water, and that this signal is then passed on to atmospheric CO(2) by biosphere-atmosphere gas exchange. We show how the decay time of the El Nino anomaly in this data set can be useful in constraining global gross primary production. Our analysis shows a rapid recovery from El Nino events, implying a shorter cycling time of CO(2) with respect to the terrestrial biosphere and oceans than previously estimated. Our analysis suggests that current estimates of global gross primary production, of 120 petagrams of carbon per year, may be too low, and that a best guess of 150-175 petagrams of carbon per year better reflects the observed rapid cycling of CO(2). Although still tentative, such a revision would present a new benchmark by which to evaluate global biospheric carbon cycling models.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Welp, Lisa R -- Keeling, Ralph F -- Meijer, Harro A J -- Bollenbacher, Alane F -- Piper, Stephen C -- Yoshimura, Kei -- Francey, Roger J -- Allison, Colin E -- Wahlen, Martin -- England -- Nature. 2011 Sep 28;477(7366):579-82. doi: 10.1038/nature10421.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Scripps Institution of Oceanography, University of California San Diego, 9500 Gilman Drive, La Jolla, California 92093-0244, USA. lwelp@ucsd.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/21956330" target="_blank"〉PubMed〈/a〉
    Keywords: Atmosphere/*chemistry ; Carbon Cycle/physiology ; Carbon Dioxide/*analysis/*chemistry ; Crops, Agricultural/metabolism ; *El Nino-Southern Oscillation ; Humidity ; Oxygen Isotopes/*analysis ; Rain ; Soil/analysis/chemistry ; Trees/metabolism ; Water/metabolism
    Print ISSN: 0028-0836
    Electronic ISSN: 1476-4687
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
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  • 3
    Publication Date: 2006-11-18
    Description: We report measurements and analysis of a boreal forest fire, integrating the effects of greenhouse gases, aerosols, black carbon deposition on snow and sea ice, and postfire changes in surface albedo. The net effect of all agents was to increase radiative forcing during the first year (34 +/- 31 Watts per square meter of burned area), but to decrease radiative forcing when averaged over an 80-year fire cycle (-2.3 +/- 2.2 Watts per square meter) because multidecadal increases in surface albedo had a larger impact than fire-emitted greenhouse gases. This result implies that future increases in boreal fire may not accelerate climate warming.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Randerson, J T -- Liu, H -- Flanner, M G -- Chambers, S D -- Jin, Y -- Hess, P G -- Pfister, G -- Mack, M C -- Treseder, K K -- Welp, L R -- Chapin, F S -- Harden, J W -- Goulden, M L -- Lyons, E -- Neff, J C -- Schuur, E A G -- Zender, C S -- New York, N.Y. -- Science. 2006 Nov 17;314(5802):1130-2.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Department of Earth System Science, University of California, Irvine, CA 92697, USA. jranders@uci.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/17110574" target="_blank"〉PubMed〈/a〉
    Keywords: Ecosystem ; *Fires ; *Greenhouse Effect ; *Trees
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Publication Date: 2013-08-10
    Description: Seasonal variations of atmospheric carbon dioxide (CO2) in the Northern Hemisphere have increased since the 1950s, but sparse observations have prevented a clear assessment of the patterns of long-term change and the underlying mechanisms. We compare recent aircraft-based observations of CO2 above the North Pacific and Arctic Oceans to earlier data from 1958 to 1961 and find that the seasonal amplitude at altitudes of 3 to 6 km increased by 50% for 45 degrees to 90 degrees N but by less than 25% for 10 degrees to 45 degrees N. An increase of 30 to 60% in the seasonal exchange of CO2 by northern extratropical land ecosystems, focused on boreal forests, is implicated, substantially more than simulated by current land ecosystem models. The observations appear to signal large ecological changes in northern forests and a major shift in the global carbon cycle.〈br /〉〈span class="detail_caption"〉Notes: 〈/span〉Graven, H D -- Keeling, R F -- Piper, S C -- Patra, P K -- Stephens, B B -- Wofsy, S C -- Welp, L R -- Sweeney, C -- Tans, P P -- Kelley, J J -- Daube, B C -- Kort, E A -- Santoni, G W -- Bent, J D -- New York, N.Y. -- Science. 2013 Sep 6;341(6150):1085-9. doi: 10.1126/science.1239207. Epub 2013 Aug 8.〈br /〉〈span class="detail_caption"〉Author address: 〈/span〉Scripps Institution of Oceanography, University of California, San Diego, La Jolla, CA, USA. hgraven@ucsd.edu〈br /〉〈span class="detail_caption"〉Record origin:〈/span〉 〈a href="http://www.ncbi.nlm.nih.gov/pubmed/23929948" target="_blank"〉PubMed〈/a〉
    Keywords: Arctic Regions ; Atmosphere/*chemistry ; *Carbon Cycle ; Carbon Dioxide/*chemistry ; *Ecosystem ; Oceans and Seas ; Seasons ; *Trees
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 5
    Publication Date: 2006-01-01
    Print ISSN: 0148-0227
    Electronic ISSN: 2156-2202
    Topics: Geosciences
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  • 6
  • 7
    Publication Date: 2016-01-18
    Description: Increasing atmospheric humidity and convective precipitation over land provide evidence of intensification of the hydrologic cycle – an expected response to surface warming. The extent to which terrestrial ecosystems modulate these hydrologic factors is important to understanding feedbacks in the climate system. We measured the oxygen and hydrogen isotope composition of water vapor from a very tall tower (185 m) in the Upper Midwest, United States to help diagnose the sources, transport, and fractionation of water vapor in the planetary boundary layer (PBL) over a 3-year period (2010 to 2012). These measurements represent the first set of annual water vapor isotope observations for the region. Models and cross wavelet analyses were used to assess the importance of Rayleigh, evapotranspiration (ET), and PBL entrainment processes on the isotope composition of water vapor. The vapor isotope composition at this tall tower site showed a very large seasonal amplitude (mean monthly δ18Ov ranged from −40.1 to −15.5 ‰ and δ2Hv ranged from −278.7 to −109.1 ‰) and followed the familiar Rayleigh distillation relation with water vapor mixing ratio at the annual time-scale. However, this relation was strongly modulated by ET and PBL entrainment processes at time-scales ranging from hours to several days. The wavelet coherence spectra indicate that the oxygen isotope ratio and the deuterium excess (dx) of water vapor are sensitive to synoptic and PBL processes. According to the phase of the coherence analyses, we show that ET often leads changes in dx, confirming that it is a potential tracer of regional ET. Isotope mixing models indicate that on average about 31 % of the growing season PBL water vapor is derived from regional ET. However, isoforcing calculations and mixing model analyses for high PBL water vapor mixing ratios events (〉 25 mmol mol−1) indicate that regional ET can account for 40 % to 60 % of the PBL water vapor. These estimates are in relatively good agreement with that derived from numerical weather model simulations. This relatively large fraction of ET-derived water vapor implies that ET has an important impact on the precipitation recycling ratio within the region. Based on multiple constraints, we estimate that the summer season recycling fraction is about 30 %, indicating a potentially important link with convective precipitation.
    Electronic ISSN: 1680-7375
    Topics: Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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  • 8
    Publication Date: 2013-05-14
    Description: In preparation for routine deployment in a network of greenhouse gas monitoring stations, we have designed and tested a simple method for drying ambient air to near or below 0.2% (2000 ppm) mole fraction H2O using a Nafion dryer. The inlet system was designed for use with cavity ring-down spectrometer (CRDS) analyzers such as the Picarro model G2301 that measure H2O in addition to their principal analytes, in this case CO2 and CH4. These analyzers report dry-gas mixing ratios without drying the sample by measuring H2O mixing ratio at the same frequency as the main analytes, and then correcting for the dilution and peak broadening effects of H2O on the mixing ratios of the other analytes measured in moist air. However, it is difficult to accurately validate the water vapor correction in the field. By substantially lowering the amount of H2O in the sample, uncertainties in the applied water vapor corrections can be reduced by an order of magnitude or more, thus eliminating the need to determine instrument-specific water vapor correction coefficients and to verify the stability over time. Our Nafion drying inlet system takes advantage of the extra capacity of the analyzer pump to redirect 30% of the dry gas exiting the Nafion to the outer shell side of the dryer and has no consumables. We tested the Nafion dryer against a cryotrap (−97 °C) method for removing H2O and found that in wet-air tests, the Nafion reduces the CO2 dry-gas mixing ratios of the sample gas by as much as 0.1 ± 0.01 ppm due to leakage across the membrane. The effect on CH4 was smaller and varied within ± 0.2 ppb, with an approximate uncertainty of 0.1 ppb. The Nafion-induced CO2 bias is partially offset by sending the dry reference gases through the Nafion dryer as well. The residual bias due to the impact of moisture differences between sample and reference gas on the permeation through the Nafion was approximately −0.05 ppm for CO2 and varied within ± 0.2 ppb for CH4. The uncertainty of this partial drying method is within the WMO compatibility guidelines for the Northern Hemisphere, 0.1 ppm for CO2 and 2 ppb for CH4, and is comparable to experimentally determining water vapor corrections for each instrument but less subject to concerns of possible drift in these corrections.
    Print ISSN: 1867-1381
    Electronic ISSN: 1867-8548
    Topics: Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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  • 9
  • 10
    Publication Date: 2012-08-07
    Description: In preparation for the routine deployment of the Earth Networks greenhouse gas monitoring network, we have designed and tested a simple method for drying ambient air to below 0.2% mole fraction H2O using a Nafion dryer. The inlet was designed for use with a Picarro model G2301 cavity ring down spectrometer (CRDS) CO2/CH4/H2O analyzer. The analyzer measures water vapor mixing ratio at the same frequency as CO2 and CH4 and then corrects for the dilution and peak broadening effects of H2O on the CO2 and CH4 mixing ratios. This analyzer is remarkably stable and performs well on water vapor correction tests, but there is potentially an added benefit of reducing the dependence on the H2O correction for long term field measurement programs. Substantially lowering the amount of H2O in the sample can reduce uncertainties in the applied H2O corrections by an order of magnitude or more, and eliminate the need to determine an instrument-specific H2O correction factor and to verify its stability over time. Our Nafion drying inlet system takes advantage of the extra capacity of the analyzer pump to redirect 30% of the dry gas exiting the Nafion to the outer shell side of the dryer and has no consumables. We tested the Nafion dryer against a cryotrap (−95 °C) method for removing H2O and found that it does not significantly alter the CO2 and CH4 dry mixing ratios of the sample gas. Systematic differences between the drying methods were at the level of 0.05 ppm in CO2 and 0.1 ppb in CH4 for the wet-air tests, well within the WMO compatibility guidelines.
    Electronic ISSN: 1867-8610
    Topics: Geosciences
    Published by Copernicus on behalf of European Geosciences Union.
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