A mechanism for biologically-induced iodine emissions from sea-ice

International audienceOnly recently, ground- and satellite-based measurements have reported high concentrations of IO in coastal Antarctica. The sources of such a large iodine burden in the Antarctic atmosphere remain unknown. We propose a novel mechanism for iodine release from sea-ice surfaces. The release is triggered by the biological production of iodide (I-) and hypoiodous acid (HOI) from marine algae, contained within and underneath sea-ice, and their diffusion through sea-ice brine channels to accumulate in the quasi-liquid layer on the surface of sea-ice. A multiphase chemical model of polar atmospheric chemistry has been developed to investigate the biology-ice-atmosphere coupling in the polar environment. Model simulations were conducted to interpret recent observations of elevated IO in the coastal Antarctic springtime. The results show that the levels of inorganic iodine (i.e. I2, IBr, ICl) released from sea-ice through this mechanism account for the observed IO concentrations in the Antarctic springtime environment. The model results also indicate that iodine may trigger the catalytic release of bromine from sea-ice through phase equilibration of IBr. Considering the extent of sea-ice around the Antarctic continent, we suggest that the resulting high levels of iodine may have widespread impact on catalytic ozone destruction and aerosol formation in the Antarctic lower troposphere

Multiphase modeling of nitrate photochemistry in the quasi-liquid layer (QLL): implications for NOx release from the Arctic and coastal Antarctic snowpack

We utilize a multiphase model, CON-AIR (<B>Con</B>densed Phase to <B>Air</B> Transfer Model), to show that the photochemistry of nitrate (NO₃^&minus;) in and on ice and snow surfaces, specifically the quasi-liquid layer (QLL), can account for NO_x volume fluxes, concentrations, and [NO]/[NO₂] (γ=[NO]/[NO₂]) measured just above the Arctic and coastal Antarctic snowpack. Maximum gas phase NO_x volume fluxes, concentrations and γ simulated for spring and summer range from 5.0&times;10⁴ to 6.4&times;10⁵ molecules cm^&minus;3 s^&minus;1, 5.7&times;10⁸ to 4.8&times;10⁹ molecules cm^&minus;3, and ~0.8 to 2.2, respectively, which are comparable to gas phase NO_x volume fluxes, concentrations and γ measured in the field. The model incorporates the appropriate actinic solar spectrum, thereby properly weighting the different rates of photolysis of NO₃^&minus; and NO₂^&minus;. This is important since the immediate precursor for NO, for example, NO₂^&minus;, absorbs at wavelengths longer than nitrate itself. Finally, one-dimensional model simulations indicate that both gas phase boundary layer NO and NO₂ exhibit a negative concentration gradient as a function of height although [NO]/[NO₂] are approximately constant. This gradient is primarily attributed to gas phase reactions of NO_x with halogens oxides (i.e. as BrO and IO), HO_x, and hydrocarbons, such as CH₃O₂

Ozone profile observations in Houston, Texas (1994 - 2010) from aircraft, balloons, and satellites

Houston, Texas has long been an urban area plagued with high levels of surface ozone, particularly in spring and late summer. The combination of a large commuter population and one of the largest concentrations of petrochemical plants in the world results in abundant and nearly co-located sources of NOx and hydrocarbons. The location of Houston on the South Coast of the United States in a subtropical climate results in meteorological conditions that favor ozone production. Using MOZAIC (1994 - 2004), ozonesonde (2000, 2004 - 2010), and TES (2005 – 2010) data, we examine the evolution of ozone profiles over Houston during a period in which various strategies have been implemented to alleviate the ozone pollution problem. Using meteorological data from associated soundings and analyses, we identify and evaluate influences on the ozone profiles from natural and anthropogenic sources, as well as local and remote sources. We further investigate how these various influences have changed with time

Validation of northern latitude Tropospheric Emission Spectrometer stare ozone profiles with ARC-IONS sondes during ARCTAS: sensitivity, bias and error analysis

We compare Tropospheric Emission Spectrometer (TES) versions 3 and 4, V003 and V004, respectively, nadir-stare ozone profiles with ozonesonde profiles from the Arctic Intensive Ozonesonde Network Study (ARCIONS, http://croc.gsfc.nasa.gov/arcions/ during the Arctic Research on the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) field mission. The ozonesonde data are from launches timed to match Aura's overpass, where 11 coincidences spanned 44° N to 71° N from April to July 2008. Using the TES "stare" observation mode, 32 observations are taken over each coincidental ozonesonde launch. By effectively sampling the same air mass 32 times, comparisons are made between the empirically-calculated random errors to the expected random errors from measurement noise, temperature and interfering species, such as water. This study represents the first validation of high latitude (>70°) TES ozone. We find that the calculated errors are consistent with the actual errors with a similar vertical distribution that varies between 5% and 20% for V003 and V004 TES data. In general, TES ozone profiles are positively biased (by less than 15%) from the surface to the upper-troposphere (~1000 to 100 hPa) and negatively biased (by less than 20%) from the upper-troposphere to the lower-stratosphere (100 to 30 hPa) when compared to the ozonesonde data. Lastly, for V003 and V004 TES data between 44° N and 71° N there is variability in the mean biases (from −14 to +15%), mean theoretical errors (from 6 to 13%), and mean random errors (from 9 to 19%)

New Insights into Martian Atmospheric Chemistry

HO_x radicals are produced in the Martian atmosphere by the photolysis of water vapor and subsequently participate in catalytic cycles that recycle carbon dioxide (CO_2) from its photolysis product carbon monoxide (CO), providing a qualitative explanation for the stability of its atmosphere. Balancing CO_2 production and loss based on our current understanding of Martian gas-phase chemistry has, however, proven to be difficult. The photolysis of O_3 produces O(^1D), while oxidation of CO produces HOCO radicals, a new member of the HO_x family. The O(^1D) quantum yield has recently been updated, which quantifies nonzero quantum yields in the Huggins bands. In Earth’s atmosphere HOCO is considered to be unimportant since it is quickly removed by abundant oxygen molecules. The smaller amount of O_2 in the Mars’ atmosphere causes HOCO’s lifetime to be longer in Mars’ atmosphere than Earth’s (3 × 10^(-5) seconds to 1.2 days from Mars’s surface to 240 km, respectively). Limited kinetic data on reactions involving HOCO prevented consideration of its reactions directly in atmospheric models. Therefore, the impact of HOCO reactions on Martian chemistry is currently unknown. Here, we incorporate new literature rate constants for HOCO chemistry and an updated representation of the O(^1D) quantum yield in the Caltech/JPL 1-D photochemical model for Mars’ atmosphere. Our simulations exemplify perturbations to NO_y, HO_x, and CO_x species, ranging from 5 to 50%. The modified O(^1D) quantum yield and new HOCO chemistry cause a 10% decrease and a 50% increase in OH and H_2O_2 total column abundances, respectively. At low altitudes, HOCO production contributes 5% towards CO_2 production. Given recent experimentally-obtained branching ratios for the oxidation of CO, HOCO may contribute up to 70% toward the production of NO_y, where HO_x and NO_y species are enhanced up to a factor 3, which has implications for rethinking the fundamental understanding of NO_y, HO_x, and CO/CO_2 cycling on Mars. Two new reaction mechanisms for converting CO to CO_2 using HOCO reactions are proposed, which reveal that H_2O_2 is more intimately coupled to CO_x chemistry. Our simulations are in good agreement with satellite/spacecraft measurements of CO and H_2O_2 on Mars

Potential significance of photoexcited NO2 on global air quality with the NMMB/BSC chemical transport model

Atmospheric chemists have recently focused on the relevance of the NO2* + H2O → OH + HONO reaction to local air quality. This chemistry has been considered not relevant for the troposphere from known reaction rates until nowadays. New experiments suggested a rate constant of 1.7 × 10−13 cm3 molecule−1 s−1, which is an order of magnitude faster than the previously estimated upper limit of 1.2 × 10−14 cm3 molecule−1 s−1, determined by Crowley and Carl (1997). Using the new global model, NMMB/BSC Chemical Transport Model (NMMB/BSC-CTM), simulations are presented that assess the potential significance of this chemistry on global air quality. Results show that if the NO2* chemistry is considered following the upper limit kinetics recommended by Crowley and Carl (1997), it produces an enhancement of ozone surface concentrations of 4–6 ppbv in rural areas and 6–15 ppbv in urban locations, reaching a maximum enhancement of 30 ppbv in eastern Asia. Moreover, NO2 enhancements are minor (xemissions are present; however, differences are small in most parts of the globe

The effect of the novel HO_2 + NO → HNO_3 reaction channel at South Pole, Antarctica

It is well established that the reaction of HO_2 with NO plays a central role in atmospheric chemistry, by way of OH/HO_2 recycling and reduction of ozone depletion by HO_x cycles in the stratosphere and through ozone production in the troposphere. Utilizing a photochemical box model, we investigate the impact of the recently observed HNO_3 production channel (HO_2+NO → HNO_3) on NO_x (NO + NO_2), HO_x (OH + HO_2), HNO_3, and O_3 concentrations in the boundary layer at the South Pole, Antarctica. Our simulations exemplify decreases in peak O_3, NO, NO_2, and OH and an increase in HNO_3. Also, mean OH is in better agreement with observations, while worsening the agreement with O_3, HO_2, and HNO_3 concentrations observed at the South Pole. The reduced concentrations of NO_x are consistent with expected decreases in atmospheric NO_x lifetime as a result of increased sequestration of NO_x into HNO_3. Although we show that the inclusion of the novel HNO_3 production channel brings better agreement of OH with field measurements, the modelled ozone and HNO_3 are worsened, and the changes in NO_x lifetime imply that snowpack NO_x emissions and snowpack nitrate recycling must be re-evaluated