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Seasonal stratospheric photochemistry on Uranus and Neptune
The file associated with this record is under embargo until 12 months after publication, in accordance with the publisher's self-archiving policy. The full text may be available through the publisher links provided above. ; A time-variable 1D photochemical model is used to study the distribution of stratospheric hydrocarbons as a function of altitude, latitude, and season on Uranus and Neptune. The results for Neptune indicate that in the absence of stratospheric circulation or other meridional transport processes, the hydrocarbon abundances exhibit strong seasonal and meridional variations in the upper stratosphere, but that these variations become increasingly damped with depth due to increasing dynamical and chemical time scales. At high altitudes, hydrocarbon mixing ratios are typically largest where the solar insolation is the greatest, leading to strong hemispheric dichotomies between the summer-to-fall hemisphere and winter-to-spring hemisphere. At mbar pressures and deeper, slower chemistry and diffusion lead to latitude variations that become more symmetric about the equator. On Uranus, the stagnant, poorly mixed stratosphere confines methane and its photochemical products to higher pressures, where chemistry and diffusion time scales remain large. Seasonal variations in hydrocarbons are therefore predicted to be more muted on Uranus, despite the planet's very large obliquity. Radiative-transfer simulations demonstrate that latitude variations in hydrocarbons on both planets are potentially observable with future JWST mid-infrared spectral imaging. Our seasonal model predictions for Neptune compare well with retrieved C 2 H 2 and C 2 H 6 abundances from spatially resolved ground-based observations (no such observations currently exist for Uranus), suggesting that stratospheric circulation — which was not included in these models — may have little influence on the large-scale meridional hydrocarbon distributions on Neptune, unlike the situation on Jupiter and Saturn. ; This material is based on research supported by the National Aeronautics and Space Administration (NASA) Science Mission Directorate under grant NNX13AH81G from the Planetary Atmospheres Research Program. The oxygen chemistry portion was supported by NASA grant NNX13AG55G. Fletcher was supported by a Royal Society Research Fellowship and European Research Council Consolidator Grant (under the European Union's Horizon 2020 research and innovation programme, grant agreement No. 723890) at the University of Leicester. Orton acknowledges support from NASA to the Jet Propulsion Laboratory, California Institute of Technology. ; Peer-reviewed ; Post-print
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Photochemistry and Signaling Activities of Plant Cryptochromes. Review
In: Известия Российской академии наук. Серия биологическая, Issue 3, p. 235-245
Cryptochromes compose the widespread class of blue-light sensory receptors that in plants regulate processes of development and circadian rhythm. These photoreceptors can also function as magnetoreceptors. Cryptochrome proteins bind flavin adenine dinucleotide (FAD) as a chromophore in the photolyase homology region (PHR) domain and contain the C-terminal extension (CCE) which is joined to PHR near the FAD-binding site. The cryptochrome activation is initiated by photochemical FAD conversions involving electron/proton transfer and the formation of redox forms. In plants, cryptochrome protein with photoreduced FAD undergoes conformational changes causing disengagement of the PHR domain and CCE that is accompanied by the formation of functionally active oligomers of cryptochrome molecules. Photooligomerization is considered as a key process necessary for cryptochrome signaling activity.
Photochemistry, mixing and diurnal cycles in the upper ocean
In: Journal of marine research, Volume 53, Issue 3, p. 341-369
ISSN: 1543-9542
Photochemistry of phenylurea herbicides and their reactions in the environment
In: Ecotoxicology and environmental safety: EES ; official journal of the International Society of Ecotoxicology and Environmental safety, Volume 5, Issue 4, p. 503-512
ISSN: 1090-2414
Photochemistry in Real Space: Batho- and Hypsochromism in the Water Dimer
We gratefully acknowledge nancial support from CONACyT/Mexico (grant 253776 and PhD scholarship 436154 for AFA), PAPIIT/UNAM (project IN205118), the Spanish MICINN (grant PGC2018-095953-B-I00), and the Principado de Asturias Government (grant FCGRUPIN- IDI/2018/000117). We are also grateful to DGTIC/UNAM (grant LANCAD-UNAMDGTIC- 250) for computer time.
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Effects of climate change on surface-water photochemistry: a review
In: Environmental science and pollution research: ESPR, Volume 21, Issue 20, p. 11770-11780
ISSN: 1614-7499
Environmental photocatalysis and photochemistry for a sustainable world: a big challenge
In: Environmental science and pollution research: ESPR, Volume 24, Issue 14, p. 12503-12505
ISSN: 1614-7499
The handbook of environmental chemistry, Reactions and processes, Pt. L, Environmental photochemistry
In: The handbook of environmental chemistry
In: Reactions and processes Pt. L
Basic study of photochemistry for application to advanced nuclear fuel cycle technology
In: Progress in nuclear energy: the international review journal covering all aspects of nuclear energy, Volume 32, Issue 3-4, p. 403-410
ISSN: 0149-1970
Environmental photochemistry of fluoroquinolones in soil and in aqueous soil suspensions under solar light
In: Environmental science and pollution research: ESPR, Volume 21, Issue 23, p. 13215-13221
ISSN: 1614-7499
Using sulfur bridge oxidation to control electronic coupling and photochemistry in covalent anthracene dimers
Covalently tethered bichromophores provide an ideal proving ground to develop strategies for controlling excited state behavior in chromophore assemblies. In this work, optical spectroscopy and electronic structure theory are combined to demonstrate that the oxidation state of a sulfur linker between anthracene chromophores gives control over not only the photophysics but also the photochemistry of the molecules. Altering the oxidation state of the sulfur linker does not change the geometry between chromophores, allowing electronic effects between chromophores to be isolated. Previously, we showed that excitonic states in sulfur-bridged terthiophene dimers were modulated by electronic screening of the sulfur lone pairs, but that the sulfur orbitals were not directly involved in these states. In the bridged anthracene dimers that are the subject of the current paper, the atomic orbitals of the unoxidized S linker can actively mix with the anthracene molecular orbitals to form new electronic states with enhanced charge transfer character, different excitonic coupling, and rapid (sub-nanosecond) intersystem crossing that depends on solvent polarity. However, the fully oxidized SO2 bridge restores purely through-space electronic coupling between anthracene chromophores and inhibits intersystem crossing. Photoexcitation leads to either internal conversion on a sub-20 picosecond timescale, or to the creation of a long-lived emissive state that is the likely precursor of the intramolecular [4 + 4] photodimerization. These results illustrate how chemical modification of a single atom in the covalent bridge can dramatically alter not only the photophysics but also the photochemistry of molecules ; This work was supported by the Basque Government (IT588-13) and the Spanish Government MINECO/FEDER (CT2016-80955-P). C. C. is indebted to the European Research Council (ERC-2016-STG-714870) for a postdoctoral contract. M. O. W. acknowledges support from the Natural Sciences and Engineering Research Council. C. J. B. acknowledges support from the National Science Foundation grant CHE-1800187
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Aquatic photochemistry of paracetamol in the presence of dissolved organic chromophoric material and nitrate
In: Environmental science and pollution research: ESPR, Volume 19, Issue 6, p. 2259-2270
ISSN: 1614-7499
Influence of the aerosol solar extinction on photochemistry during the 2010 Russian wildfires episode
In this work, impact of aerosol solar extinction on the photochemistry over eastern Europe during the 2010 wildfires episode is discussed for the period from 5 to 12 August 2010, which coincides to the peak of fire activity. The methodology is based on an online coupling between the chemistry-transport model CHIMERE (extended by an aerosol optical module) and the radiative transfer code TUV. Results of simulations indicate an important influence of the aerosol solar extinction, in terms of intensity and spatial extent, with a reduction of the photolysis rates of NO2 and O-3 up to 50% (in daytime average) along the aerosol plume transport. At a regional scale, these changes in photolysis rates lead to a 3-15% increase in the NO2 daytime concentration and to an ozone reduction near the surface of 1-12 %. The ozone reduction is shown to occur over the entire boundary layer, where aerosols are located. Also, the total aerosol mass concentration (PM10) is shown to be decreased by 1-2 %, on average during the studied period, caused by a reduced formation of secondary aerosols such as sulfates and secondary organics (4-10 %) when aerosol impact on photolysis rates is included. In terms of model performance, comparisons of simulations with air quality measurements at Moscow indicate that an explicit representation of aerosols interaction with photolysis rates tend to improve the estimation of the near-surface concentration of ozone and nitrogen dioxide as well as the formation of inorganic aerosol species such as ammonium, nitrates and sulfates.
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