Abstract
Abstract. The structure and amplitude of the radiative contributions of the annual cycles in ozone and water vapour to the prominent annual cycle in temperatures in the tropical tropopause layer (TTL) are considered. This is done initially through a seasonally evolving fixed dynamical heating (SEFDH) calculation. The annual cycle in ozone is found to drive significant temperature changes predominantly locally (in the vertical) and roughly in phase with the observed TTL annual cycle. In contrast, temperature changes driven by the annual cycle in water vapour are out of phase with the latter. The effects are weaker than those of ozone but still quantitatively significant, particularly near the cold point (100 to 90 hPa) where there are substantial non-local effects from variations in water vapour in lower layers of the TTL. The combined radiative heating effect of the annual cycles in ozone and water vapour maximizes above the cold point and is one factor contributing to the vertical structure of the amplitude of the annual cycle in lower-stratospheric temperatures, which has a relatively localized maximum around 70 hPa. Other important factors are identified here: radiative damping timescales, which are shown to maximize over a deep layer centred on the cold point; the vertical structure of the dynamical heating; and non-radiative processes in the upper troposphere that are inferred to impose a strong constraint on tropical temperature perturbations below 130 hPa. The latitudinal structure of the radiative contributions to the annual cycle in temperatures is found to be substantially modified when the SEFDH assumption is relaxed and the dynamical response, as represented by a zonally symmetric calculation, is taken into account. The effect of the dynamical response is to reduce the strong latitudinal gradients and inter-hemispheric asymmetry seen in the purely radiative SEFDH temperature response, while leaving the 20° N–20° S average response relatively unchanged. The net contribution of the annual ozone and water vapour cycles to the peak-to-peak amplitude in the annual cycle of TTL temperatures is found to be around 35 % of the observed 8 K at 70 hPa, 40 % of 6 K at 90 hPa, and 45 % of 3 K at 100 hPa. The primary sensitivity of the calculated magnitude of the temperature response is identified as the assumed annual mean ozone mixing ratio in the TTL.
Highlights
The tropical tropopause layer (TTL), spanning from 150 to 70 hPa or 14 to 18.5 km, is the main entry region for air into the stratosphere from the troposphere (e.g. Fueglistaler et al, 2009)
We investigate, first using the seasonally evolving fixed dynamical heating (SEFDH) approach, the individual and combined radiative effects of the annual cycles in ozone and water vapour on TTL temperatures, including at 70 hPa where the amplitude of the annual cycle is at a maximum and at 90 hPa near the cold point which is crucial for determining stratospheric water vapour mixing ratios
The SEFDH temperature changes are sensitive to the background ozone mixing ratios and a set of further calculations is presented in Appendix C. (The results presented in Sect. 3 are in broad agreement with those from similar work by Gilford and Solomon (2017), which we became aware of during the review process.) Section 4 discusses the vertical structure of the annual cycle in temperature, distinguishing the role of the background radiative environment from that of the radiative and dynamical heating in determining this structure
Summary
The tropical tropopause layer (TTL), spanning from 150 to 70 hPa or 14 to 18.5 km, is the main entry region for air into the stratosphere from the troposphere (e.g. Fueglistaler et al, 2009). To study the radiative contributions of seasonal variations in ozone and water vapour to the annual cycle in TTL temperatures, we make use of the seasonally evolving fixed dynamical heating calculation (Forster et al, 1997). This method calculates the time-varying temperature change due to a specified radiative perturbation (e.g. a change in a trace gas) and takes into account the specified time dependence of temperature and trace gas concentration profiles in a background state to which the perturbation is applied.
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