Coming to America: Multiple Origins of New World Geckos

Geckos in the Western Hemisphere provide an excellent model to study faunal assembly at a continental scale. We generated a time-calibrated phylogeny, including exemplars of all New World gecko genera, to produce a biogeographic scenario for the New World geckos. Patterns of New World gecko origins are consistent with almost every biogeographic scenario utilized by a terrestrial vertebrate with different New World lineages showing evidence of vicariance, dispersal via temporary land bridge, overseas dispersal, or anthropogenic introductions. We also recovered a strong relationship between clade age and species diversity, with older New World lineages having more species than more recently arrived lineages. Our data provide the first phylogenetic hypothesis for all New World geckos and highlight the intricate origins and ongoing organization of continental faunas. The phylogenetic and biogeographical hypotheses presented here provide an historical framework to further pursue research on the diversification and assembly of the New World herpetofauna

Stratospheric Dynamical Response and Ozone Feedbacks in the Presence of SO_2 Injections

Injections of sulfur dioxide into the stratosphere are among several proposed methods of solar radiation management. Such injections could cool the Earth's climate. However, they would significantly alter the dynamics of the stratosphere. We explore here the stratospheric dynamical response to sulfur dioxide injections ∼5 km above the tropopause at multiple latitudes (equator, 15°S, 15°N, 30°S and 30°N) using a fully coupled Earth system model, Community Earth System Model, version 1, with the Whole Atmosphere Community Climate Model as its atmospheric component (CESM1(WACCM)). We find that in all simulations, the tropical lower stratosphere warms primarily between 30°S and 30°N, regardless of injection latitude. The quasi-biennial oscillation (QBO) of the tropical zonal wind is altered by the various sulfur dioxide injections. In a simulation with a 12 Tg yr^(−1) equatorial injection, and with fully interactive chemistry, the QBO period lengthens to ∼3.5 years but never completely disappears. However, in a simulation with specified (or noninteractive) chemical fields, including O_3 and prescribed aerosols taken from the interactive simulation, the oscillation is virtually lost. In addition, we find that geoengineering does not always lengthen the QBO. We further demonstrate that the QBO period changes from 24 to 12–17 months in simulations with sulfur dioxide injections placed poleward of the equator. Our study points to the importance of understanding and verifying of the complex interactions between aerosols, atmospheric dynamics, and atmospheric chemistry as well as understanding the effects of sulfur dioxide injections placed away from the Equator on the QBO

The Climate Response to Stratospheric Aerosol Geoengineering Can Be Tailored Using Multiple Injection Locations

By injecting different amounts of SO_2 at multiple different latitudes, the spatial pattern of aerosol optical depth (AOD) can be partially controlled. This leads to the ability to influence the climate response to geoengineering with stratospheric aerosols, providing the potential for design. We use simulations from the fully coupled whole-atmosphere chemistry climate model CESM1(WACCM) to demonstrate that by appropriately combining injection at just four different locations, 30°S, 15°S, 15°N, and 30°N, then three spatial degrees of freedom of AOD can be achieved: an approximately spatially uniform AOD distribution, the relative difference in AOD between Northern and Southern Hemispheres, and the relative AOD in high versus low latitudes. For forcing levels that yield 1–2°C cooling, the AOD and surface temperature response are sufficiently linear in this model so that the response to different combinations of injection at different latitudes can be estimated from single-latitude injection simulations; nonlinearities associated with both aerosol growth and changes to stratospheric circulation will be increasingly important at higher forcing levels. Optimized injection at multiple locations is predicted to improve compensation of CO_2-forced climate change relative to a case using only equatorial aerosol injection (which overcools the tropics relative to high latitudes). The additional degrees of freedom can be used, for example, to balance the interhemispheric temperature gradient and the equator to pole temperature gradient in addition to the global mean temperature. Further research is needed to better quantify the impacts of these strategies on changes to long-term temperature, precipitation, and other climate parameters

Sensitivity of Aerosol Distribution and Climate Response to Stratospheric SO_2 Injection Locations

Injection of SO_2 into the stratosphere has been proposed as a method to, in part, counteract anthropogenic climate change. So far, most studies investigated injections at the equator or in a region in the tropics. Here we use Community Earth System Model version 1 Whole Atmosphere Community Climate Model (CESM1(WACCM)) to explore the impact of continuous single grid point SO_2 injections at seven different latitudes and two altitudes in the stratosphere on aerosol distribution and climate. For each of the 14 locations, 3 different constant SO_2 emission rates were tested to identify linearity in aerosol burden, aerosol optical depth, and climate effects. We found that injections at 15°N and 15°S and at 25 km altitude have equal or greater effect on radiation and surface temperature than injections at the equator. Nonequatorial injections transport SO_2 and sulfate aerosols more efficiently into middle and high latitudes and result in particles of smaller effective radius and larger aerosol burden in middle and high latitudes. Injections at 15°S produce the largest increase in global average aerosol optical depth and increase the change in radiative forcing per Tg SO_2/yr by about 15% compared to equatorial injections. High-altitude injections at 15°N produce the largest reduction in global average temperature of 0.2° per Tg S/yr for the last 7 years of a 10 year experiment. Injections at higher altitude are generally more efficient at reducing surface temperature, with the exception of large equatorial injections of at least 12 Tg SO_2/yr. These findings have important implications for designing a strategy to counteract global climate change

A comparison of electrochemical degradation of phenol on boron doped diamond and lead dioxide anodes

This work compares two electrode materials used to mineralize phenol contained in waste waters. Two disks covered with either boron doped diamond (BDD) or PbO2 were used as anodes in a one compartment flow cell under the same hydrodynamic conditions. Efficiencies of galvanostatic electrolyses are compared on the basis of measurements of Total Organic Carbon (TOC) and Chemical Oxygen Demand (COD). Galvanostatic electrolyses were monitored by analysis of phenol and of its oxidation derivatives to evaluate the operating time needed for complete elimination of toxic aromatics. The experimental current efficiency is close to the theoretical value for the BDD electrode. Other parameters being equal, phenol species disappeared at the same rate using the two electrode materials but the BDD anode showed better efficiency to eliminate TOC and COD. Moreover, during the electrolysis less intermediates are formed with BDD compared to PbO2 whatever the current density. A comparison of energy consumption is given based on the criterion of 99% removal of aromatic compounds

Effects of Different Stratospheric SO_2 Injection Altitudes on Stratospheric Chemistry and Dynamics

Strategically applied geoengineering is proposed to reduce some of the known side effects of stratospheric aerosol modifications. Specific climate goals could be reached depending on design choices of stratospheric sulfur injections by latitude, altitude, and magnitude. Here we explore in detail the stratospheric chemical and dynamical responses to injections at different altitudes using a fully coupled Earth System Model. Two different scenarios are explored that produce approximately the same global cooling of 2°C over the period 2042–2049, a high‐altitude injection case using 24 Tg SO_2/year at 30 hPa (≈25‐km altitude) and a low‐altitude injection case using 32 Tg SO_2/year injections at 70 hPa (between 19‐ and 20‐km altitude), with annual injections divided equally between 15°N and 15°S. Both cases result in a warming of the lower tropical stratosphere up to 10 and 15°C for the high‐ and low‐altitude injection case and in substantial increases of stratospheric water vapor of up to 2 and 4 ppm, respectively, compared to no geoengineering conditions. Polar column ozone in the Northern Hemisphere is reduced by up to 18% in March for the high‐altitude injection case and up to 8% for the low‐altitude injection case. However, for winter middle and high northern latitudes, low‐altitude injections result in greater column ozone values than without geoengineering. These changes are mostly driven by dynamics and advection. Antarctic column ozone in 2042–2049 does not recover from present‐day (2002–2009) values for both cases

Short- and medium-term atmospheric constituent effects of very large solar proton events

International audienceSolar eruptions sometimes produce protons, which impact the Earth's atmosphere. These solar proton events (SPEs) generally last a few days and produce high energy particles that precipitate into the Earth's atmosphere. The protons cause ionization and dissociation processes that ultimately lead to an enhancement of odd-hydrogen and odd-nitrogen in the polar cap regions (>60° geomagnetic latitude). We have used the Whole Atmosphere Community Climate Model (WACCM3) to study the atmospheric impact of SPEs over the period 1963?2005. The very largest SPEs were found to be the most important and caused atmospheric effects that lasted several months after the events. We present the short- and medium-term (days to a few months) atmospheric influence of the four largest SPEs in the past 45 years (August 1972; October 1989; July 2000; and October?November 2003) as computed by WACCM3 and observed by satellite instruments. Polar mesospheric NOx (NO+NO2) increased by over 50 ppbv and mesospheric ozone decreased by over 30% during these very large SPEs. Changes in HNO3, N2O5, ClONO2, HOCl, and ClO were indirectly caused by the very large SPEs in October?November 2003, were simulated by WACCM3, and previously measured by Envisat Michelson Interferometer for Passive Atmospheric Sounding (MIPAS). WACCM3 output was also represented by sampling with the MIPAS averaging kernel for a more valid comparison. Although qualitatively similar, there are discrepancies between the model and measurement with WACCM3 predicted HNO3 and ClONO2 enhancements being smaller than measured and N2O5 enhancements being larger than measured. The HOCl enhancements were fairly similar in amounts and temporal variation in WACCM3 and MIPAS. WACCM3 simulated ClO decreases below 50 km, whereas MIPAS mainly observed increases, a very perplexing difference. Upper stratospheric and lower mesospheric NOx increased by over 10 ppbv and was transported during polar night down to the middle stratosphere in several weeks past the SPE. The WACCM3 simulations confirmed the SH HALOE observations of enhanced NOx in September 2000 as a result of the July 2000 SPE and the NH SAGE II observations of enhanced NO2 in March 1990 as a result of the October 1989 SPEs

Stratospheric Response in the First Geoengineering Simulation Meeting Multiple Surface Climate Objectives

We describe here changes in stratospheric dynamics and chemistry in a first century‐long sulfate aerosol geoengineering simulation in which the mean surface temperature and the interhemispheric and equator‐to‐pole surface temperature gradients were kept near their 2020 levels despite the RCP8.5 emission scenario. Simulations were carried out with the Community Earth System Model, version 1 with the Whole Atmosphere Community Climate Model as its atmospheric component [CESM1(WACCM)] coupled to a feedback algorithm controlling the magnitude of sulfur dioxide (SO_2) injections at four injection latitudes. We find that, throughout the entire geoengineering simulation, the lower stratospheric temperatures increase by ∼0.19 K per Tg SO_2 injection per year or ∼10 K with ∼40 Tg SO_2/year total SO_2 injection. These temperature changes are associated with a strengthening of the polar jets in the stratosphere and weakening of the mean zonal wind in the lower stratosphere subtropics and throughout the troposphere, associated with weaker storm track activity. In the geoengineering simulation the quasi‐biennial oscillation of the tropical lower stratospheric winds remains close to the presently observed quasi‐biennial oscillation, even for large amounts of SO2 injection. Water vapor in the stratosphere increases substantially: by 25% with ∼20 Tg SO_2/year annual injection and by up to 90% with a ∼40 Tg SO_2/year injection. Stratospheric column ozone in the geoengineering simulation is predicted to recover to or supersede preozone hole conditions by the end of the century

Electrochemical polymerisation of phenol in aqueous solution on a Ta/PbO2 anode

This paper deals with the treatment of aqueous phenol solutions using an electrochemical technique. Phenol can be partly eliminated from aqueous solution by electrochemically initiated polymerisation. Galvanostatic electrolyses of phenol solutions at concentration up to 0.1 mol dm−3 were carried out on a Ta/PbO2 anode. The polymers formed are insoluble in acidic medium but soluble in alkaline. These polymers were filtered and then dissolved in aqueous solution of sodium hydroxide (1 mol dm−3). The polymers formed were quantified by total organic carbon (TOC) measurement. It was found that the conversion of phenol into polymers increases as a function of initial concentration, anodic current density, temperature, and solution pH. The percentage of phenol polymerised can reach 15%