20,417 research outputs found

    Tropospheric temperature response to stratospheric ozone recovery in the 21st century

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    Recent simulations predicted that the stratospheric ozone layer will likely return to pre-1980 levels in the middle of the 21st century, as a result of the decline of ozone depleting substances under the Montreal Protocol. Since the ozone layer is an important component in determining stratospheric and tropospheric-surface energy balance, the recovery of stratospheric ozone may have significant impact on tropospheric-surface climate. Here, using multi-model results from both the Intergovernmental Panel on Climate Change Fourth Assessment Report (IPCC-AR4) models and coupled chemistry-climate models, we show that as ozone recovery is considered, the troposphere is warmed more than that without considering ozone recovery, suggesting an enhancement of tropospheric warming due to ozone recovery. It is found that the enhanced tropospheric warming is mostly significant in the upper troposphere, with a global and annual mean magnitude of ~0.41 K for 2001–2050. We also find that relatively large enhanced warming occurs in the extratropics and polar regions in summer and autumn in both hemispheres, while the enhanced warming is stronger in the Northern Hemisphere than in the Southern Hemisphere. Enhanced warming is also found at the surface. The global and annual mean enhancement of surface warming is about 0.16 K for 2001–2050, with maximum enhancement in the winter Arctic

    Extended radio emission after the soft X-ray maximum of the NOAA 9077 AR solar flare on July 10, 2000

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    An extended radio emission after a soft X-ray (SXR) maximum was detected in the active region NOAA 9077 by several observatories for the solar flare after 21:42 UT on July 10, 2000. Also some radio fine structures before the enduring radio emission were observed with the 1.0-2.0 GHz spectrometer of Beijing Astronomical Observatory (BAO) in the same time. We apply a shear-driven quadrupolar reconnection model (SQR) to analyze the fine structures and the related radio emission. We find that the footpoint shear motion of the flux loop is accompanied with the emerging up of the loop during the reconnection process. We tentatively interpret the extended radio emission as the nonthermal radiation caused by a new reconnection process between emerging flux loop and pre-existing overarching loop after the soft X-ray maximum

    Momentum Distribution of Near-Zero-Energy Photoelectrons in the Strong-Field Tunneling Ionization in the Long Wavelength Limit

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    We investigate the ionization dynamics of Argon atoms irradiated by an ultrashort intense laser of a wavelength up to 3100 nm, addressing the momentum distribution of the photoelectrons with near-zero-energy. We find a surprising accumulation in the momentum distribution corresponding to meV energy and a \textquotedblleft V"-like structure at the slightly larger transverse momenta. Semiclassical simulations indicate the crucial role of the Coulomb attraction between the escaping electron and the remaining ion at extremely large distance. Tracing back classical trajectories, we find the tunneling electrons born in a certain window of the field phase and transverse velocity are responsible for the striking accumulation. Our theoretical results are consistent with recent meV-resolved high-precision measurements.Comment: 5 pages, 4 figure

    Seasonal variations of stable carbon isotopic composition and biogenic tracer compounds of water-soluble organic aerosols in a deciduous forest

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    To investigate the seasonal changes in biogenic water-soluble organic carbon (WSOC) aerosols in a boreal forest, aerosol samples were collected continuously in the canopy of a deciduous forest in northern Japan during 2009–2010. Stable carbon isotopic composition of WSOC (δ<sup>13</sup>C<sub>WSOC</sub>) in total suspended particulate matter (TSP) exhibited a distinct seasonal cycle, with lower values from June through September (−25.5±0.5 ‰). This cycle follows the net CO<sub>2</sub> exchange between the forest ecosystem and the atmosphere, indicating that δ<sup>13</sup>C<sub>WSOC</sub> likely reflects the biological activity at the forest site. WSOC concentrations showed the highest values in early summer and autumn. Positive matrix factorization (PMF) analysis indicated that the factor in which biogenic secondary organic aerosols (BSOAs) dominated accounted for ~40 % of the highest concentrations of WSOC, where BSOAs mostly consisted of α-/β-pinene SOA. In addition, primary biological aerosol particles (PBAPs) made similar contributions (~57 %) to the WSOC near the forest floor in early summer. This finding indicates that the production of both primary and secondary WSOC aerosols is important during the growing season in a deciduous forest. The methanesulfonic acid (MSA) maximum was also found in early summer and had a distinct vertical gradient with larger concentrations near the forest floor. Together with the similar vertical gradients found for WSOC and δ<sup>13</sup>C<sub>WSOC</sub> as well as the α-/β-pinene SOA tracers, our results indicate that the forest floor, including ground vegetation and soil, acts as a significant source of WSOC in TSP within a forest canopy at the study site
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