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  • 1
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1995
    In:  Eos, Transactions American Geophysical Union Vol. 76, No. 21 ( 1995-05-23), p. 214-214
    In: Eos, Transactions American Geophysical Union, American Geophysical Union (AGU), Vol. 76, No. 21 ( 1995-05-23), p. 214-214
    Abstract: Since 1986 the Atmospheric Environment Service (AES) of Environment Canada has operated an atmospheric chemistry program at Station Alert, which is located at 82°N on the northern tip of Ellesmere Island. The program provides a detailed record of atmospheric change in the high Arctic that is crucial to both regional and global issues. Plans to reduce the Canadian government's deficit now require Environment Canada to make budgetary cuts and are prompting reevaluation of this and other programs. In light of these circumstances, we would like to take the opportunity to consider the importance of Alert to international atmospheric science.
    Type of Medium: Online Resource
    ISSN: 0096-3941 , 2324-9250
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1995
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  • 2
    Online Resource
    Online Resource
    Stockholm University Press ; 2011
    In:  Tellus B Vol. 63, No. 1 ( 2011-2-1)
    In: Tellus B, Stockholm University Press, Vol. 63, No. 1 ( 2011-2-1)
    Type of Medium: Online Resource
    ISSN: 1600-0889 , 0280-6509
    RVK:
    RVK:
    Language: Unknown
    Publisher: Stockholm University Press
    Publication Date: 2011
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  • 3
    In: Global Biogeochemical Cycles, American Geophysical Union (AGU), Vol. 10, No. 3 ( 1996-09), p. 431-456
    Abstract: A generalized terrestrial ecosystem process model, BIOME‐BGC (for BIOME BioGeoChemical Cycles), was used to simulate the global fluxes of CO 2 resulting from photosynthesis, autotrophic respiration, and heterotrophic respiration. Daily meteorological data for the year 1987, gridded to 1° by 1°, were used to drive the model simulations. From the maximum value of the normalized difference vegetation index (NDVI) for 1987, the leaf area index for each grid cell was computed. Global NPP was estimated to be 52 Pg C, and global R h was estimated to be 66 Pg C. Model predictions of the stable carbon isotopic ratio 13 C/ 12 C for C 3 and C 4 vegetation were in accord with values published in the literature, suggesting that our computations of total net photosynthesis, and thus NPP, are more reliable than R h . For each grid cell, daily R h was adjusted so that the annual total was equal to annual NPP, and the resulting net carbon fluxes were used as inputs to a three‐dimensional atmospheric transport model (TM2) using wind data from 1987. We compared the spatial and seasonal patterns of NPP with a diagnostic NDVI model, where NPP was derived from biweekly NDVI data and R h was tuned to fit atmospheric CO 2 observations from three northern stations. To an encouraging degree, predictions from the BIOME‐BGC model agreed in phase and amplitude with observed atmospheric CO 2 concentrations for 20° to 55°N, the zone in which the most complete data on ecosystem processes and meteorological input data are available. However, in the tropics and high northern latitudes, disagreements between simulated and measured CO 2 concentrations indicated areas where the model could be improved. We present here a methodology by which terrestrial ecosystem models can be tested globally, not by comparisons to homogeneous‐plot data, but by seasonal and spatial consistency with a diagnostic NDVI model and atmospheric CO 2 observations.
    Type of Medium: Online Resource
    ISSN: 0886-6236 , 1944-9224
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1996
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  • 4
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1985
    In:  Journal of Geophysical Research: Atmospheres Vol. 90, No. D6 ( 1985-10-20), p. 10511-10528
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 90, No. D6 ( 1985-10-20), p. 10511-10528
    Abstract: From May 1959 to June 1981 the concentration of atmospheric carbon dioxide was measured in 2419 samples of air collected on a weather ship situated at 50°N and 145°W in the North Pacific Ocean. Three principal characteristics of the variation in concentration of atmospheric CO 2 are revealed by these data: an annual variation that repeats with nearly the same pattern each year, an interannual variation that correlates with the large‐scale circulation of the atmosphere, and a long‐term increase that is nearly proportional to the global input of CO 2 from the combustion of fossil fuels. The peak‐to‐trough amplitude of the smoothed annual signal increased from 13.3 ppm in 1969 to 14.5 ppm in 1981. The phasing of the annual CO 2 cycle suggests a close relation to the activity of land plants in the broad region of the northern hemisphere where plants grow mainly during the summer. The increasing amplitude suggests a heightening plant activity. The interannual variation and its first derivative correlate with the Southern Oscillation. A lag of 6 months in the derivative suggests a distant oceanic or terrestrial source‐sink in the tropics or southern hemisphere. The seasonally adjusted CO 2 concentration increased from 324.9 ppm in May 1969 to 340.8 ppm in June 1981. This increase is 60% of the increase that would have occurred if all the CO 2 from fossil fuel combustion had remained in the atmosphere and had been uniformly distributed there. The seasonally adjusted concentration, when averaged from 1975 to 1981, is 0.8 ppm lower than that found at Point Barrow, Alaska, at 71°N and 0.9 ppm higher than that found at Mauna Loa Observatory, Hawaii, at 19°N, suggesting a steadily decreasing concentration in CO 2 from north to south in the broad band from 70°N to 20°N.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1985
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  • 5
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1986
    In:  Journal of Geophysical Research: Atmospheres Vol. 91, No. D7 ( 1986-06-20), p. 7765-7781
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 91, No. D7 ( 1986-06-20), p. 7765-7781
    Abstract: An extensive set of atmospheric CO 2 observations were obtained during the First Global Geophysical Experiment (FGGE) Hawaii to Tahiti Shuttle expedition of 1979–1980. These data have been examined using a one‐dimensional meridional diffusive transport model of the atmospheric circulation. The observed CO 2 concentration field was first decomposed into three parts: a seasonal component consisting of two harmonic functions of time, with periods of 1 year and 6 months; a mean annual north‐south concentration profile; and a linear trend with time, independent of latitude. In the first of two papers interpreting these data, we consider which features of the north‐south eddy transport are revealed by the seasonal component of the CO 2 concentration field. We assume that the FGGE data represent a zonally and vertically uniform CO 2 field, and we restrict our analysis to the latitude belt between 14.5°N and 14.5°S, where seasonal sources and sinks of CO 2 have minimal influence on the atmospheric CO 2 concentration. The strongest feature of the CO 2 data for calibrating the model is the steadily diminishing amplitude of the annual harmonic from north to south. We show that in the absence of sources and sinks the magnitude of the eddy diffusion coefficient as a function of latitude can be prescribed from this amplitude, provided that two additional quantities are specified at a single reference location. These additional quantities are the amplitude of the first harmonic of the seasonal flux and the phase difference between that harmonic and the first harmonic of the local concentration signal. Selecting 14.5°S for this reference location, we find through comparisons of the model prediction with the FGGE CO 2 data that the diffusion coefficient depends primarily on the selected amplitude of the seasonal flux and is practically independent of the phase difference. On the basis of the goodness of fit of the model predictions to the CO 2 data, we set a lower limit on this flux amplitude, corresponding to an average eddy diffusion coefficient of 4.6 × 10 9 cm 2 s −1 . This is equivalent to an upper limit of 1.4 years on the interhemispheric exchange time for CO 2 . We are unable to set an upper limit on the diffusion coefficient because the phasing of the first harmonic in the FGGE data shifts so slightly with latitude that even very large diffusion coefficients yield satisfactory model predictions of the seasonal CO 2 concentration field. The relative variation in the diffusion coefficient with latitude, which is derived solely from the amplitude of the first harmonic of the CO 2 data, reveals two zones of resistance to interhemispheric CO 2 exchange. One, near 8°N, corresponds to the well‐known intertropical convergence zone of the wind field which exists around the entire earth. The second, near 8°S, correlates with a weaker wind convergence zone in the central Pacific. This regional feature evidently affects the CO 2 concentration field in the vicinity of the FGGE data set, but it may not represent a global feature.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1986
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  • 6
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1980
    In:  Geophysical Research Letters Vol. 7, No. 7 ( 1980-07), p. 505-508
    In: Geophysical Research Letters, American Geophysical Union (AGU), Vol. 7, No. 7 ( 1980-07), p. 505-508
    Abstract: Knowledge of recent global changes in the rare isotopic species 13 CO 2 in atmospheric carbon dioxide does not now distinguish whether the land biosphere is a source or sink for fossil fuel carbon dioxide. The question is critically dependent on isotopic fractionation between the atmosphere and ocean water: if the isotopic fractionation factor for CO 2 uptake at the air‐ocean boundary, α am , is approximately 0.986, as is the case for strongly alkaline solutions, the 13 CO 2 content of atmospheric CO 2 is insensitive to changes in the biosphere; if α am is approximately unity, as now seems likely for ocean water, very accurate measurements, over the next decade or longer, will permit an estimate to be made of the net global loss or gain of biospheric carbon.
    Type of Medium: Online Resource
    ISSN: 0094-8276 , 1944-8007
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1980
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  • 7
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1968
    In:  Journal of Geophysical Research Vol. 73, No. 14 ( 1968-07-15), p. 4529-4541
    In: Journal of Geophysical Research, American Geophysical Union (AGU), Vol. 73, No. 14 ( 1968-07-15), p. 4529-4541
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1968
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  • 8
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1983
    In:  Journal of Geophysical Research: Oceans Vol. 88, No. C15 ( 1983-12-20), p. 10915-10933
    In: Journal of Geophysical Research: Oceans, American Geophysical Union (AGU), Vol. 88, No. C15 ( 1983-12-20), p. 10915-10933
    Abstract: Between March 1977 and February 1982, 517 samples of air were collected in 51 glass flasks at four stations in the northern hemisphere near the Pacific ocean and at the South Pole. First, the CO 2 concentration of each sample was determined by nondispersive infrared gas analysis, and then the 13 C/ 12 C and 18 O/ 16 O ratios of the cryogenic extracted CO 2 were determined with a triple collector mass spectrometer. For each station the secular trend and seasonal variation in 13 C/ 12 C ratio have been established as a function of CO 2 concentration. The seasonally adjusted 13 C/ 12 C ratio is found to have decreased at a rate of about 0.02‰ per ppm increase in the seasonally adjusted CO 2 concentration and to vary with latitude as expected if CO 2 is being released by fossil fuel combustion in the northern hemisphere and from ocean water near the equator. At the three northernmost stations (La Jolla, California, at 33°N and two Hawaiian stations near 19°N) the 13 C/ 12 C ratio of the CO 2 added to and withdrawn from the atmosphere during one annual cycle is circa −29‰ with respect to standard PDB, as expected from the exchange of atmospheric CO 2 with the carbon of terrestrial plants. Near the equator at Fanning Island (4°N) the similarly computed 13 C/ 12 C ratio is −21‰, while at the South Pole it is about −13‰. This suggests that the seasonal variation in the southern hemisphere and tropics is partially a result of oceanic CO 2 exchange.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1983
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  • 9
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1965
    In:  Journal of Geophysical Research Vol. 70, No. 24 ( 1965-12-15), p. 6077-6085
    In: Journal of Geophysical Research, American Geophysical Union (AGU), Vol. 70, No. 24 ( 1965-12-15), p. 6077-6085
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1965
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    detail.hit.zdb_id: 2220777-6
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    SSG: 16,13
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  • 10
    Online Resource
    Online Resource
    Stockholm University Press ; 1960
    In:  Tellus Vol. 12, No. 2 ( 1960-05), p. 200-203
    In: Tellus, Stockholm University Press, Vol. 12, No. 2 ( 1960-05), p. 200-203
    Type of Medium: Online Resource
    ISSN: 0040-2826 , 2153-3490
    URL: Issue
    Language: English
    Publisher: Stockholm University Press
    Publication Date: 1960
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