Corrigendum to "Fractional release factors of long-lived halogenated organic compounds in the tropical stratosphere" published in Atmos. Chem. Phys., 10, 1093–1103, 2010

We have noted a computational error in the calculation of the averaged Fractional Release Factors (FRFs) relative to the averaged FRF of CFCl3 (CFC-11). ..

The effect of desiccation on the emission of volatile bromocarbons from two common temperate macroalgae

Exposure of intertidal macroalgae during low tide has been linked to the emission of a variety of atmospherically-important trace gases into the coastal atmosphere. In recent years, several studies have investigated the role of inorganic iodine and organoiodides as antioxidants and their emission during exposure to combat oxidative stress, yet the role of organic bromine species during desiccation is less well understood. In this study the emission of dibromomethane (CH2Br2) and bromoform (CHBr3) during exposure and desiccation of two common temperate macroalgae, Fucus vesiculosus and Ulva intestinalis, is reported. Determination of the impact exposure may have on algal physiological processes is difficult as intertidal species are adapted to desiccation and may undergo varying degrees of desiccation before their physiology is affected. For this reason we include comparisons between photosynthetic capacity (Fv/Fm) and halocarbon emissions during a desiccation time series. In addition, the role of rewetting with freshwater to simulate exposure to rain was also investigated. Our results show that an immediate flux of bromocarbons occurs upon exposure, followed by a decline in bromocarbon emissions. We suggest that this immediate bromocarbon pulse may be linked to volatilisation or emissions of existing bromocarbon stores from the algal surface rather than the production of bromocarbons as an antioxidant response

Directionality between driven-dissipative resonators

The notion of nonreciprocity, in essence when going forwards is different from going backwards, emerges in all branches of physics from cosmology to electromagnetism. Intriguingly, the breakdown of reciprocity is typically associated with extraordinary phenomena, which may be readily capitalized on in the design of (for example) nontrivial electromagnetic devices when Lorentz reciprocity is broken. However, in order to enable the exploitation of nonreciprocal-like effects in the next generation of quantum technologies, basic quantum optical theories are required. Here we present a versatile model describing a pair of driven-dissipative quantum resonators, where the relative phase difference between the coherent and incoherent couplings induces an asymmetry. The interplay between the diverse dissipative landscape —which encompasses both intrinsic losses and dissipative couplings— and the coherent interactions leads to some remarkable consequences including highly directional (or even one-way) energy transport. Our work proffers the tantalizing prospect of observing dissipation-induced quantum directionality in areas like photonics or cavity magnonics (spin waves), which may aid the design of unconventional nanoscopic devices

Observation-based assessment of stratospheric fractional release, lifetimes, and ozone depletion potentials of ten important source gases

Estimates of the recovery time of stratospheric ozone heavily rely on the exact knowledge of the processes that lead to the decomposition of the relevant halogenated source gases. Crucial parameters in this context are fractional release factors (FRFs) as well as stratospheric lifetimes and ozone depletion potentials (ODPs). We here present data from the analysis of air samples collected between 2009 and 2011 on board research aircraft flying in the mid- and high-latitude stratosphere and infer the above-mentioned parameters for ten major source gases: CFCl3 (CFC-11), CF2Cl2 (CFC-12), CF2ClCFCl2 (CFC-113), CCl4 (carbon tetrachloride), CH3CCl3 (methyl chloroform), CHF2Cl (HCFC-22), CH3CFCl2 (HCFC-141b), CH3CF2Cl (HCFC-142b), CF2ClBr (H-1211), and CF3Br (H-1301). The inferred correlations of their FRFs with mean ages of air reveal less decomposition as compared to previous studies for most compounds. When using the calculated set of FRFs to infer equivalent stratospheric chlorine, we find a reduction of more than 20% as compared to the values inferred in the most recent Scientific Assessment of Ozone Depletion by the World Meteorological Organisation (WMO, 2011). We also note that FRFs and their correlations with mean age are not generally time-independent as often assumed. The stratospheric lifetimes were calculated relative to that of CFC-11. Within our uncertainties the ratios between stratospheric lifetimes inferred here agree with the values in recent WMO reports except for CFC-11, CFC-12 and CH3CCl3. Finally, we calculate lower ODPs than recommended by WMO for six out of ten compounds, with changes most pronounced for the three HCFCs. Collectively these newly calculated values may have important implications for the severity and recovery time of stratospheric ozone loss

Directionality between driven-dissipative resonators

The notion of nonreciprocity, in essence when going forwards is different from going backwards, emerges in all branches of physics from cosmology to electromagnetism. Intriguingly, the breakdown of reciprocity is typically associated with extraordinary phenomena, which may be readily capitalized on in the design of (for example) nontrivial electromagnetic devices when Lorentz reciprocity is broken. However, in order to enable the exploitation of nonreciprocal-like effects in the next generation of quantum technologies, basic quantum optical theories are required. Here we present a versatile model describing a pair of driven-dissipative quantum resonators, where the relative phase difference between the coherent and incoherent couplings induces an asymmetry. The interplay between the diverse dissipative landscape - which encompasses both intrinsic losses and dissipative couplings - and the coherent interactions leads to some remarkable consequences including highly directional (or even one-way) energy transport. Our work proffers the tantalizing prospect of observing dissipation-induced quantum directionality in areas like photonics or cavity magnonics (spin waves), which may aid the design of unconventional nanoscopic devices.Comment: 7 pages, 4 figure

Fractional release factors of long-lived halogenated organic compounds in the tropical stratosphere

Fractional release factors (FRFs) of organic trace gases are time-independent quantities that influence the calculation of Global Warming Potentials and Ozone Depletion Potentials. We present the first set of vertically resolved FRFs for 15 long-lived halocarbons in the tropical stratosphere up to 34 km altitude. They were calculated from measurements on air samples collected on board balloons and a high altitude aircraft. We compare the derived dependencies of FRFs on the mean stratospheric transit times (the so-called mean ages of air) with similarly derived FRFs originating from measurements at higher latitudes and find significant differences. Moreover a comparison with averaged FRFs currently used by the World Meteorological Organisation revealed the limitations of these measures due to their observed vertical and latitudinal variability. The presented data set could be used to improve future ozone level and climate projections

Vertical Profiles of Bromoform in Snow, Sea Ice, and Seawater in the Canadian Arctic

Bromoform (CHBr3) was measured in vertical profiles from the snow surface through the snowpack, sea ice, and water column to the seafloor at Resolute Bay, Canada, in the sprig of 1992. Elevated concentrations of bromoform were observed in both the ice (32-266 ng L-1 by liquid water volume) and seawater (~ 20 ng L-1 ) at the ice-water interface, associated with bromoform emission from ice microalgae. A surprising finding was a second horizon of high bromoform concentrations (336-367 ng L-1) in sea ice at the snow-ice interface. Chlorophyll and salinity were also elevated in this upper ice layer, although chlorophyll was much lower than in the basal ice microalgal layer. We speculate that this upper bromoformenriched layer may have originated from scavenging of the surface water layer by frazil ice during initial ice formation in the preceding autumn. Equally unexpected was the occurrence of yet higher bromoform concentrations in snowpack immediately overlying the sea ice (492-1260 ng L-1), declining in concentration (by about a factor of 2 or more) toward the snow surface. Snow of very recent origin, however, contained as little as 2 orders of magnitude less bromoform than the older snowpack. Possible origins for elevated bromoform in the snowpack include diffusion out of the bromoform-enriched upper ice layer and gradual concentration of bromoform out of the atmosphere by adsorption on to ice crystals. These are considered in turn. In one scenario, photolysis of bromoform from snow is considered, which might help account for atmospheric bromine-ozone chemistry. The possible contributions from snow, sea ice, and seawater to atmospheric bromoform levels during both the winter and spring are also considered, and it is concluded that surface seawater presents the most significant reservoir for atmospheric bromofor

Tracer Measurements in Growing Sea Ice Support Convective Gravity Drainage Parameterizations

Gravity drainage is the dominant process redistributing solutes in growing sea ice. Modeling gravity drainage is therefore necessary to predict physical and biogeochemical variables in sea ice. We evaluate seven gravity drainage parameterizations, spanning the range of approaches in the literature, using tracer measurements in a sea ice growth experiment. Artificial sea ice is grown to around 17 cm thickness in a new experimental facility, the Roland von Glasow air‐sea‐ice chamber. We use NaCl (present in the water initially) and rhodamine (injected into the water after 10 cm of sea ice growth) as independent tracers of brine dynamics. We measure vertical profiles of bulk salinity in situ, as well as bulk salinity and rhodamine in discrete samples taken at the end of the experiment. Convective parameterizations that diagnose gravity drainage using Rayleigh numbers outperform a simpler convective parameterization and diffusive parameterizations when compared to observations. This study is the first to numerically model solutes decoupled from salinity using convective gravity drainage parameterizations. Our results show that (1) convective, Rayleigh number‐based parameterizations are our most accurate and precise tool for predicting sea ice bulk salinity; and (2) these parameterizations can be generalized to brine dynamics parameterizations, and hence can predict the dynamics of any solute in growing sea ic

A new multi-gas constrained model of trace gas non-homogeneous transport in firn: evaluation and behaviour at eleven polar sites

Insoluble trace gases are trapped in polar ice at the firn-ice transition, at approximately 50 to 100 m below the surface, depending primarily on the site temperature and snow accumulation. Models of trace gas transport in polar firn are used to relate firn air and ice core records of trace gases to their atmospheric history. We propose a new model based on the following contributions. First, the firn air transport model is revised in a poromechanics framework with emphasis on the non-homogeneous properties and the treatment of gravitational settling. We then derive a nonlinear least square multi-gas optimisation scheme to calculate the effective firn diffusivity (automatic diffusivity tuning). The improvements gained by the multi-gas approach are investigated (up to ten gases for a single site are included in the optimisation process). We apply the model to four Arctic (Devon Island, NEEM, North GRIP, Summit) and seven Antarctic (DE08, Berkner Island, Siple Dome, Dronning Maud Land, South Pole, Dome C, Vostok) sites and calculate their respective depth-dependent diffusivity profiles. Among these different sites, a relationship is inferred between the snow accumulation rate and an increasing thickness of the lock-in zone defined from the isotopic composition of molecular nitrogen in firn air (denoted d15N). It is associated with a reduced diffusivity value and an increased ratio of advective to diffusive flux in deep firn, which is particularly important at high accumulation rate sites. This has implications for the understanding of d15N of N2 records in ice cores, in relation with past variations of the snow accumulation rate. As the snow accumulation rate is clearly a primary control on the thickness of the lock-in zone, our new approach that allows for the estimation of the lock-in zone width as a function of accumulation may lead to a better constraint on the age difference between the ice and entrapped gases