Engineering topics

Matthews, W. Andrew

Publications and source records attributed to Matthews, W. Andrew.

7 records

NASA NTRS1994

Infrared spectroscopic measurements of the total column abundance of ethan (C2H6) above Lauder, New Zealand

Total vertical column aboundances of atmospheric ethane (C2H6) have been retrieved form more than 350 high-resolution infrared solar spectra recorded on 129 days between December 1992 and March 1994 at the Network for the Detection of Stratospheric Change (NDSC) station in Lauder, New Zealand (latitude 45.04 deg S, 169.68 deg E, 0.37 km altitude). The results are based on nonlinear least squares fits to narrow spectral intervals containing the unresolved C2H6 nu (sub 7) band (P)Q(sub 3) and (R)Q(sub 0) subbranches at 2976.8 and 2986.7/cm. The measured Lauder column abundances show a pronounced seasonal cycle with a maximum value of (8.6 +/- 0.5) x 10(exp 15) molecules/sq cm in September and a minimum value of (3.8 +/- 0.5) x 10 (exp 15) molecules/sq cm in February. Assuming a realistic vertical distribution for C2H6, these values correspond to surface level volume-mixing ratios of 0.52 and 0.23 ppbv (parts per billion by volume), respectively. The phase and relative amplitude of the Lauder C2H6 seasonal cycle are similar to corresponding values determined from infrared measurements at the Jungfraujoch (46.55 deg N, 7.98 deg E, 3.58 km altitude) and Mauna Loa (latitude 19.5 deg N, longitude 155.6 deg W, 3.5 km altitude) NDSC stations, but the inferred absolute magnitudes of the Lauder surface level mixing ratios during the same season are significantly lower. The Lauder C2H6 measurements are also compared with published southern hemisphere surface level sampling measurements and two-dimensional model calculations.

Rinsland, Curtis P.↗

NASA NTRS1994

Southern hemisphere ground based measurements of Carbonyl Fluoride (COF2) and Hydrogen Fluoride (HF): Partitioning between Fluoride reservoir species

We report infrared ground based total column measurements of the stratospheric fluorine reservoir gases COF2 and HF above Lauder, New Zealand (45 deg S, 167.8 deg E) obtained between April 1993 and January 1994. The average retrieved COF2 and HF total columns are 2.81(+/- 0.56) x 10(exp 14) and 9.91(+/- 1.09) x 10(exp 14) molecules/sq cm respectively. The daily average COF2 and HF columns are correlated; this correlation is likely the result of dynamics. The average HF/COF2 column ratio on days with measurements of both HF and COF2 is 3.63 (+/- 0.55). Comparison of this ratio with model calculations implies that the quantum yield for COF2 photolysis is near unity. Our measured COF2 columns are higher than all previously reported values, but inconsistencies among the earlier measurements and uncertainty in the latitudinal gradient of the COF2 column preclude an accurate determination of the long-term COF2 trend.

Reisinger, Andreas R.↗

NASA NTRS1994

Tropospheric ozone at 45 deg S

In August of 1986 a program was initiated to measure atmospheric ozone profiles at mid-latitudes in the Southern Hemisphere by flying ECC ozonesondes on a regular basis from the DSIR Physical Sciences Atmospheric Laboratory at Lauder, New Zealand, 45 deg S. Flights since that time have been performed on a regular basis at the rate of two flights per week during the 5 month period August to December, the time of maximum variability at mid-latitudes, and once per week for the remainder of the year. These data, consisting now of more than 400 profiles has been analyzed and the free troposphere portion of the profiles binned as 1km slabs. These data have been combined to form a seasonal average values for each season of each year in 2 km slabs and the variation observed in these seasonal averages is the basis of this paper. A biennial component is apparent in these data and the lack of any increasing trend over this 5 year period is contrasted with that measured at similar latitudes in the Northern Hemisphere over the same period.

Matthews, W. Andrew↗

NASA NTRS1994

Seasonal cycle in atmospheric HCl at 45 deg S

High resolution Fourier transform infrared interferometric atmospheric solar absorption measurements have been performed at the National Institute for Water and Atmospheric Research Laboratory at Lauder, New Zealand on a routine basis since October 1989. This laboratory has been selected as the Mid-latitude Charter Site of the Network for the Detection of Stratospheric Change and is at a latitude of 45 deg S. Particular attention has been paid to the absorption by atmospheric hydrogen chloride at 2925.9 cm(exp -1) and in this paper the results of the seasonal cycle in CHl above Lauder will be presented. Because of the very clean troposphere at this site, the CHl column measured from the ground is essentially a stratospheric column measurement.

Matthews, W. Andrew↗

NASA NTRS1991

Stratospheric processes: Observations and interpretation

Explaining the observed ozone trends discussed in an earlier update and predicting future trends requires an understanding of the stratospheric processes that affect ozone. Stratospheric processes occur on both large and small spatial scales and over both long and short periods of time. Because these diverse processes interact with each other, only in rare cases can individual processes be studied by direct observation. Generally the cause and effect relationships for ozone changes were established by comparisons between observations and model simulations. Increasingly, these comparisons rely on the developing, observed relationships among trace gases and dynamical quantities to initialize and constrain the simulations. The goal of this discussion of stratospheric processes is to describe the causes for the observed ozone trends as they are currently understood. At present, we understand with considerable confidence the stratospheric processes responsible for the Antarctic ozone hole but are only beginning to understand the causes of the ozone trends at middle latitudes. Even though the causes of the ozone trends at middle latitudes were not clearly determined, it is likely that they, just as those over Antarctica, involved chlorine and bromine chemistry that was enhanced by heterogeneous processes. This discussion generally presents only an update of the observations that have occurred for stratospheric processes since the last assessment (World Meteorological Organization (WMO), 1990), and is not a complete review of all the new information about stratospheric processes. It begins with an update of the previous assessment of polar stratospheres (WMO, 1990), followed by a discussion on the possible causes for the ozone trends at middle latitudes and on the effects of bromine and of volcanoes.

Brune, William H.↗

NASA NTRS1989

Evidence of the mid-latitude impact of Antarctic ozone depletion

Record low ozone values found over Australia and New Zealand during December 1987 following the record low Antarctic values of October 1987 are analyzed. The sudden decline of ozone amounts in midmonth rule out photochemical effects as a cause and permit the underlying processes to be investigated on a case study basis. Using data from ozone sondes, radiosondes, the Nimbus-7 total ozone mapping spectrometer, and meteorological analyses from the National Meteorological Center, it is argued that these low values resulted from transport of ozone-poor air from higher latitudes. Thus, it seems that the chemical destruction of ozone over Antarctica in early spring is having an impact on lower latitudes.

Atkinson, Roger J.↗

NASA NTRS1988

Diurnal variation of nitric oxide at 32 km - Measurements and interpretation

Balloon observations of NO and ozone near sunset and sunrise around 32 km were made on September 19 and October 4, 1985 from Aire sur l'Adour, France. The NO concentration built up rapidly after sunrise, remained fairly steady during the day, and decreased slowly near sunset. This variation is interpreted quantitatively in terms of current photochemistry in relation to ozone.

Kondo, Yutaka↗