Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1998
    In:  Journal of Geophysical Research: Atmospheres Vol. 103, No. D5 ( 1998-03-20), p. 5729-5746
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 103, No. D5 ( 1998-03-20), p. 5729-5746
    Abstract: Continuous measurements of alkyl nitrates were made during the Tropospheric Ozone Research subproject of the European Experiment on Transport and Transformation of Environmentally Relevant Trace Constituents in the Troposphere Over Europe at the Schauinsland station in the Black Forest between June 1990 and May 1991, using an automated gas chromatograph with a NO y detector. More than 2000 samples were analyzed with a sampling frequency of six to nine samples per day. The mixing ratio of the sum of alkyl nitrates (C 1 ‐C 8 ) ranged between 30 and 630 parts per trillion (ppt) and averaged 120 ppt over the whole measurement period. The average contribution of alkyl nitrates to total odd nitrogen was about 3%, with little seasonal variation. The most abundant individual nitrates were 2‐propyl, 2‐butyl, and methyl nitrate. When lumped by carbon number, the sum of C 5 nitrates represented the largest fraction after methyl nitrate. The mixing ratios of nitrates ≥C 7 were very small. In polluted air masses, the mixing ratios of alkyl nitrates exhibited summer maxima and pronounced daily variations, with maxima in the early evening. The abundance increased from C 3 to C 5 . In clean, photochemically aged air masses, alkyl nitrate mixing ratios showed a summer minimum and no pronounced diurnal variations. A decrease of abundance from C 3 toward higher carbon chain lengths was observed, as is expected for air that is characterized by photochemical destruction. The measured concentration ratios between different alkyl nitrate isomers are utilized to resolve discrepancies in the existing data on branching ratios for the formation of alkyl nitrates from the reaction of peroxy radicals with NO and to classify air masses with respect to photochemical age. The observed behavior and mixing ratios of methyl and ethyl nitrate cannot be explained by formation solely from the reaction of peroxy radicals and NO.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1998
    detail.hit.zdb_id: 2033040-6
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    American Geophysical Union (AGU) ; 1996
    In:  Journal of Geophysical Research: Atmospheres Vol. 101, No. D13 ( 1996-08-20), p. 18613-18627
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 101, No. D13 ( 1996-08-20), p. 18613-18627
    Abstract: A set of photoelectric detectors for airborne measurements of the photolysis frequency of NO 2 , i.e., J NO 2 , was developed and integrated aboard the research aircraft Hercules C‐130 operated by the U.K. Meteorological Office. The instrument consists of two separate sensors, each of which provides an isotropic response over a solid angle of 2π steradian (sr). The sensors are mounted on top and below the aircraft, respectively, to obtain a field of view of 4π sr, and permit the discrimination of the upwelling and downwelling components of the actinic flux. From experimental tests and model calculations it is demonstrated that small differences between the spectral sensitivity of the sensors and the spectral response of J NO 2 can lead to significant errors in the determination of J NO 2 , especially under cloudy conditions. We present correction factors for clear sky conditions and suggest the use of a new filter combination in the sensors which requires only small corrections and provides acceptable accuracy, even under cloudy conditions. A climatology of J NO 2 values is presented from a series of flights made in 1993 at latitudes of 36°–59°N. For clear sky conditions and solar zenith angles of 33°–35°, J NO 2 was 8.3 × 10 −3 s −1 at sea level and increased with altitude to values of 13 × 10 −3 s −1 at 7.5 km altitude. Above clouds, J NO 2 reached maximum values of 24 × 10 −3 s −1 , and peak values of 29 × 10 −3 s −1 were observed for very short periods in the uppermost layers of clouds. Enhancement of the actinic flux due to light scattered from clouds was also observed at altitudes below 0.5 km. Comparison of the clear sky data with predictions from different radiative transfer models reveals the best agreement for models of higher angular resolution. The Delta Eddington method underpredicts the measurements significantly, whereas the J NO 2 values predicted by the discrete ordinate method and multidirectional model are only about 5% smaller than our measurements, a difference that is within the experimental uncertainties.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 1996
    detail.hit.zdb_id: 2033040-6
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    In: Journal of Geophysical Research: Atmospheres, American Geophysical Union (AGU), Vol. 105, No. D1 ( 2000-01-20), p. 1563-1583
    Abstract: The Schauinsland Ozone Precursor Experiment (SLOPE96) campaign was conducted in June 1996 to study the physicochemical transformation of pollutants and the production of photooxidants during transport from the city of Freiburg to the Schauinsland mountain. For this purpose, chemical surface measurements were made at the entrance of the valley Großes Tal, and close to the Schauinsland summit, at 1200 m altitude on a saddle at the end of the valley. In addition, measurements of ozone, NO 2 , and meteorological parameters were made on two tethered balloons and aboard a small aircraft. This paper describes the experimental setup and the measurements of ozone, odd‐nitrogen compounds, carbonyl compounds, CO, and photolysis frequencies made during SLOPE96. The various instruments used on the different platforms were harmonized on the basis of intercomparison experiments in order to achieve a consistent picture. Large precursor concentrations from the nearby city of Freiburg are transported to Schauinsland in a valley wind system during stagnant high‐pressure conditions. These conditions occurred only on 2 days of the campaign, and only 1 day (June 5) was predictable enough to allow for deployment of the aircraft and the balloons. An OH concentration of 8 ‐ 10× 0 6 cm −3 is derived from the rate of change of HNO 3 and NO 2 on June 5 at Schauinsland (1.5–3 ppb NO 2 ; J O1 D ≈ 2 × 10 −5 s −1 ), assuming quasi steady state and a homogeneous air mass. The ozone production rate as determined from the photostationary state of NO x at Schauinsland reached maximum daily values between 15 and 60 ppb h 1 around noontime. On average, P(O 3 ) comprised about 30% of the photolysis rate of NO 2 . Similar to earlier observations at Schauinsland, a good correlation between P(O 3 ) and the product of UV radiation and precursor concentrations was found.
    Type of Medium: Online Resource
    ISSN: 0148-0227
    Language: English
    Publisher: American Geophysical Union (AGU)
    Publication Date: 2000
    detail.hit.zdb_id: 2033040-6
    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
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. Further information can be found on the KOBV privacy pages