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  • 1
    In: Journal of Molecular Spectroscopy, Elsevier BV, Vol. 327 ( 2016-09), p. 105-121
    Type of Medium: Online Resource
    ISSN: 0022-2852
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2016
    detail.hit.zdb_id: 1469771-3
    SSG: 11
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  • 2
    Online Resource
    Online Resource
    American Association for the Advancement of Science (AAAS) ; 1992
    In:  Science Vol. 256, No. 5055 ( 1992-04-17), p. 342-349
    In: Science, American Association for the Advancement of Science (AAAS), Vol. 256, No. 5055 ( 1992-04-17), p. 342-349
    Type of Medium: Online Resource
    ISSN: 0036-8075 , 1095-9203
    RVK:
    RVK:
    Language: English
    Publisher: American Association for the Advancement of Science (AAAS)
    Publication Date: 1992
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    detail.hit.zdb_id: 2066996-3
    detail.hit.zdb_id: 2060783-0
    SSG: 11
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  • 3
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 2001
    In:  Geophysical Research Letters Vol. 28, No. 12 ( 2001-06-15), p. 2369-2372
    In: Geophysical Research Letters, American Geophysical Union (AGU), Vol. 28, No. 12 ( 2001-06-15), p. 2369-2372
    Abstract: Ozone isopleths plotted with measured values of ozone, hydrocarbons and total reactive nitrogen (NOy) are proposed to visualize ozone production regimes at distinct locations. The applicability of the concept is confirmed with measurements at two distinct sites in the Italian Po Basin. Empirical ozone isopleths at the urban site clearly show ROG‐sensitive ozone production, with ozone increasing with increasing ROG concentrations and decreasing with increasing ambient levels of NOx. At the rural site NOx‐sensitive ozone production prevails, in accordance with previous results.
    Type of Medium: Online Resource
    ISSN: 0094-8276 , 1944-8007
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2001
    detail.hit.zdb_id: 2021599-X
    detail.hit.zdb_id: 7403-2
    SSG: 16,13
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  • 4
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1998
    In:  Journal of Geophysical Research: Atmospheres Vol. 103, No. D7 ( 1998-04-20), p. 8389-8399
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 103, No. D7 ( 1998-04-20), p. 8389-8399
    Abstract: Total ozone measurements have been made at Arosa, Switzerland (47°N), from 1926 through the present day, forming the longest total ozone series in the world. The record has been recently homogenized. Ozone trends are calculated to be −(2.3±0.6)% per decade for annual means (larger losses are found in winter and spring, approximately −4% per decade for trends in January, February, and March) when a simple linear change from 1970 to 1996 is assumed. In addition, total ozone trends are calculated using multiple regression models involving combinations of explanatory variables for the 11‐year solar cycle, local meteorological conditions (the Mount Säntis high‐altitude temperature record), stratospheric aerosol loading from volcanoes, and stratospheric chlorine loading. When the terms for the solar cycle, the stratospheric aerosol loading and the high mountain temperature record were included, the annually averaged ozone trends were found to be −(1.9±0.6)% per decade. While a statistically significant relation is found between total ozone and indices of aerosol loadings of the stratosphere, the recent decrease in total ozone cannot be accounted for by the higher average aerosol content in the second half of the century. Finally, the decrease in ozone in the stratosphere is estimated to be approximately 30% larger than that found for total ozone, when a crude estimate of the increase in tropospheric ozone is included. The acceleration observed in total ozone trends between the 1970s and the 1980s over northern midlatitudes [e.g., Harris et al. , 1997] might be partially attributed to the larger increase in tropospheric ozone in the 1970s.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1998
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    detail.hit.zdb_id: 2130824-X
    detail.hit.zdb_id: 2016813-5
    detail.hit.zdb_id: 2016810-X
    detail.hit.zdb_id: 2403298-0
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    detail.hit.zdb_id: 161667-5
    detail.hit.zdb_id: 2969341-X
    detail.hit.zdb_id: 161665-1
    detail.hit.zdb_id: 3094268-8
    detail.hit.zdb_id: 710256-2
    detail.hit.zdb_id: 2016804-4
    detail.hit.zdb_id: 3094181-7
    detail.hit.zdb_id: 3094219-6
    detail.hit.zdb_id: 3094167-2
    detail.hit.zdb_id: 2220777-6
    detail.hit.zdb_id: 3094197-0
    SSG: 16,13
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  • 5
    In: Atmospheric Environment, Elsevier BV, Vol. 35, No. 32 ( 2001-11), p. 5553-5566
    Type of Medium: Online Resource
    ISSN: 1352-2310
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2001
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    detail.hit.zdb_id: 1499889-0
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  • 6
    In: Atmospheric Environment, Elsevier BV, Vol. 39, No. 6 ( 2005-2), p. 1009-1018
    Type of Medium: Online Resource
    ISSN: 1352-2310
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2005
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    detail.hit.zdb_id: 1499889-0
    SSG: 14
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  • 7
    Online Resource
    Online Resource
    Oekom Publishers GmbH ; 1994
    In:  GAIA - Ecological Perspectives for Science and Society Vol. 3, No. 3 ( 1994-05-01), p. 157-169
    In: GAIA - Ecological Perspectives for Science and Society, Oekom Publishers GmbH, Vol. 3, No. 3 ( 1994-05-01), p. 157-169
    Abstract: The objective of the Swiss resarch project POLLUMET (POLLUtion and METeorology) is to investigate the formation and transport of photooxidants over the Swiss Plateau and in the surrounding pre-Alpine valleys. Extensive meteorological and air chemistry measurements were obtained during three intensive field studies conducted in the month of July of the years 1990, 1991 and 1993. The study included ground-based measurements, observations from instrumented aircraft, measurements taken with radiosondes, radars and other surface and airborne instruments. The comprehensive database is aimed to provide the information needed for the application of photochemical models and their evaluation and refinement. In order to better understand the photochemical processes which control ozone formation over the Swiss Plateau, calculations with the Harvard Photochemical Model and the Harwell Photochemical Trajectory Model were conducted and compared with experimental data. Reduction scenarios performed with both models yield in one case a NO x -limited situation for rural areas, whereas the other model predicts a transition type situation. Hydrogen peroxide was used as an indicator to study the performance of the photochemical models. Combining measurements of ozone, NO 2 and hydrogen peroxide indicates that ozone in rural areas might be reduced most effectively by NO x controls. The model results indicate, that in Switzerland emissions have to be reduced by a large amount to achieve a substantial reduction in peak values of surface ozone.
    Type of Medium: Online Resource
    ISSN: 0940-5550
    RVK:
    Language: English
    Publisher: Oekom Publishers GmbH
    Publication Date: 1994
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    detail.hit.zdb_id: 2111556-4
    detail.hit.zdb_id: 1114994-2
    SSG: 14
    SSG: 5,21
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  • 8
    Online Resource
    Online Resource
    Oekom Publishers GmbH ; 2003
    In:  GAIA - Ecological Perspectives for Science and Society Vol. 12, No. 3 ( 2003-08-01), p. 181-186
    In: GAIA - Ecological Perspectives for Science and Society, Oekom Publishers GmbH, Vol. 12, No. 3 ( 2003-08-01), p. 181-186
    Abstract: Atmospheric chemistry is a relatively young field of applied chemistry. In this article, the historical development of ozone research, representing an important branch of atmospheric chemistry, is outlined. Additionally, future focal points of ozone research are defined. In order to understand key questions in atmospheric ozone research (both for stratospheric ozone depletion and for photooxidant formation) the input from chemistry is crucial. In order to avoid that atmospheric chemistry develops into a more and more specialized and narrow discipline, I recommend that future ozone research further emphasizes the responsibility toward society and continues (and strengthens) the links to atmospheric physics.
    Type of Medium: Online Resource
    ISSN: 0940-5550
    RVK:
    Language: English
    Publisher: Oekom Publishers GmbH
    Publication Date: 2003
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    detail.hit.zdb_id: 2111556-4
    detail.hit.zdb_id: 1114994-2
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  • 9
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 2001
    In:  Journal of Geophysical Research: Atmospheres Vol. 106, No. D19 ( 2001-10-16), p. 22685-22694
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 106, No. D19 ( 2001-10-16), p. 22685-22694
    Abstract: Long‐term changes in the vertical ozone distribution over Switzerland are examined for the period 1967–2000. A statistical trend analysis is performed accounting for chemical and dynamical variability. The tropopause pressure, the North Atlantic oscillation (NAO), the Arctic oscillation (AO), and the quasi‐biennial oscillation (QBO) are used as dynamical quantities. In addition, the solar effect and an ozone depletion factor (ODF), which describes the joint effect of stratospheric chlorine and aerosol loading, are included. A term is allowed for an unexplained linear trend. The various influences on ozone are estimated employing stepwise regression. Tropopause pressure and lower stratospheric ozone (10–19 km) variability are found to be strongly linked throughout the year. The NAO‐AO indices show a negative correlation with lower stratospheric ozone in winter‐spring. A positive correlation of NAO‐AO and ozone is found in the middle stratosphere (23–30 km) during late summer to early winter. There is a solar signal in the middle stratosphere which becomes strongly significant in summer. The QBO signal is prominent at the height of the ozone maximum in winter‐spring. The unexplained trends are much larger than the contributions of the ODF, suggesting that mechanisms other than midlatitude in situ chemistry are mostly responsible for the observed ozone loss. In the lowermost stratosphere (10–15 km), the observed ozone trends are found to be caused by dynamics. Above, the residual ozone trend (in percent) is independent of height and in the range of −2% to −5% per decade up to 30 km.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2001
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    detail.hit.zdb_id: 3094104-0
    detail.hit.zdb_id: 2130824-X
    detail.hit.zdb_id: 2016813-5
    detail.hit.zdb_id: 2016810-X
    detail.hit.zdb_id: 2403298-0
    detail.hit.zdb_id: 2016800-7
    detail.hit.zdb_id: 161666-3
    detail.hit.zdb_id: 161667-5
    detail.hit.zdb_id: 2969341-X
    detail.hit.zdb_id: 161665-1
    detail.hit.zdb_id: 3094268-8
    detail.hit.zdb_id: 710256-2
    detail.hit.zdb_id: 2016804-4
    detail.hit.zdb_id: 3094181-7
    detail.hit.zdb_id: 3094219-6
    detail.hit.zdb_id: 3094167-2
    detail.hit.zdb_id: 2220777-6
    detail.hit.zdb_id: 3094197-0
    SSG: 16,13
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  • 10
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1995
    In:  Geophysical Research Letters Vol. 22, No. 1 ( 1995-01), p. 53-56
    In: Geophysical Research Letters, American Geophysical Union (AGU), Vol. 22, No. 1 ( 1995-01), p. 53-56
    Abstract: With a double monochromator, high resolution spectral measurements of direct solar UV‐irradiance were performed in Arosa during February and March, 1993. Total atmospheric ozone amount is determined by fitting model calculations to the measured spectra. The results are compared with the operationally performed measurements of a Dobson and a Brewer spectrometer. The total ozone amount determined from spectral measurements differs from the results of the Dobson instrument by −1.1±0.9% and from those of the Brewer instrument by −0.4±0.7%.
    Type of Medium: Online Resource
    ISSN: 0094-8276 , 1944-8007
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1995
    detail.hit.zdb_id: 2021599-X
    detail.hit.zdb_id: 7403-2
    SSG: 16,13
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