Source parameters of the 2001 Mw 7.7 Bhuj earthquake,Gujarat, India,aftershock sequence

We present the estimated source parameters from SH-wave spectral modeling of selected 463 aftershocks (2002–06) of the 26 January 2001 Bhuj earthquake, the well-recorded largest continental intraplate earthquake. The estimated seismic moment (M_o), corner frequency (f_c), source radius (r) and stress drop (Δσ) for aftershocks of moment magnitude 1.7 to 5.6 range from 3.55×10¹¹ to 2.84×10¹⁷ N-m, 1.3 to 11.83 Hz, 107 to 1515 m and 0.13 to 26.7 MPa, respectively, while the errors in f_c and Δσ are found to be 1.1 Hz and 1.1 MPa, respectively. We also notice that the near surface attenuation factor (k) values vary from 0.02 to 0.03. Our estimates reveal that the stress drop values show more scatter (Mo^{0.5 to 1} is proportional to Δσ) toward the larger M_o values (≥10^14.5 N-m), while they show a more systematic nature (Mo³ is proportional to Δσ) for smaller M_o values (<10^14.5 N-m), which can be explained as a consequence of a nearly constant rupture radius for smaller aftershocks in the region. The large stress drops (= 10 MPa) associated with events on the north Wagad fault (at 15–30 km depth) and Gedi fault (at 3–15 km depth) can be attributed to the large stress developed at hypocentral depths as a result of high fluid pressure and the presence of mafic intrusive bodies beneath these two fault zones.     

Role of Nitrogen Oxides,Black Carbon,and Meteorological Parameters on the Variation of Surface Ozone Levels at a Tropical Urban Site – Hyderabad,India

In this study, temporal variations of surface ozone (O₃) were investigated at tropical urban site of Hyderabad during the year 2009. O₃, oxides of nitrogen (NO_x = NO + NO₂), black carbon (BC), and meteorological parameters were continuously monitored at the established air monitoring station. Results revealed the production of surface O₃ from NO₂ through photochemical oxidation. Averaged datasets illustrated the variations in ground‐level concentrations of these air pollutants along different time scales. Maximum mean concentrations of O₃ (56.75 ppbv) and NO_x (8.9 ppbv) were observed in summer. Diurnal‐seasonal changes in surface O₃ and NO_x concentrations were explicated with complex atmospheric chemistry, boundary layer dynamics, and local meteorology. In addition, nocturnal chemistry of NO_x played a decisive role in the formation of O₃ during day time. Mean BC mass concentration in winter (10.92 µg m^?3) was high during morning hours. Heterogeneous chemistry of BC on O₃ destruction and NO_x formation was elucidated. Apart from these local observations, long‐range transport of trace gases and BC aerosols were evidenced from air mass back trajectories. Further, statistical modeling was performed to predict O₃ using multi‐linear regression method, which resulted in 91% of the overall variance.