Methanesulfonate in the Greenland Ice Sheet Project 2 Ice Core

In this paper we present measurements of methanesulfonate in the Greenland Ice Sheet Project 2 (GISP2) ice core. Methanesulfonate is an atmospheric oxidation product of dimethylsulfide. The GISP2 methanesulfonate record contains information about the atmospheric loading of biogenic sulfur over the past 110 kyr and its relationship to climate change. The GISP2 data set supports the inferences made from the Renland ice core from Greenland that the glacial atmosphere over Greenland had reduced concentrations of biogenic sulfur compared with the present day [Hansson and Saltzman, 1993]. We conclude that the flux of biogenic sulfur from the North Atlantic Ocean must have been lower during glacial times and speculate that this decrease may have been related to differences in phytoplankton speciation. The data suggest that changes in direct radiative forcing from biogenic sulfur aerosols would act as negative feedback to the glacial/interglacial climate cycles in this region

Two-hundred-year Record of Biogenic Sulfur in a South Greenland Ice Core (20D)

The concentration of methanesulfonic acid (MSA) was determined in a shallow south central Greenland ice core(20D). This study provides a high-resolution record of the DMS-derived biogenic sulfur in Greenland precipitation over the past 200 years. The mean concentration of MSA is 3.30 ppb(σ = 2.38 ppb,n = 1134). The general trend of MSA is an increase from 3.01 to 4.10 ppb between 1767 and 1900, followed by a steady decrease to 2.34 ppb at the present time. This trend is in marked contrast to that of non-sea-salt sulfate (nss SO42-), which increases dramatically after 1900 due to the input of anthropogenic sulfur. The MSA fraction ((MSA/(MSA+ nss SO42-))* 100) ranges from a mean of 15% in preindustrial ice to less than 5% in recent ice. These MSA fraction suggest that approximately 5 to 40% of the sulfur in recent Greenland ice is of biological origin. It is suggested that there is a significant low-latitude component to the biogenic sulfur in the core and that variations in the MSA fraction reflect changes in the relative strengths of low- and high-latitude inputs. The data shown o evidence for a strong dependence of dimethyl sulfide(DMS) emissions on sea surface temperature during the last century. There is also no indication that the yield of MSA from DMS oxidation has been altered by increased NOx levels over the North Atlantic during this period

An Ice-Core-Based, Late Holocene History for the Transantarctic Mountains, Antarctica

Ice core records (major anions and cations, MSA, oxygen isotopes and particles) developed from two shallow (~200 m depth) sites in the Transantarctic Mountains provide documentation of much of the Holocene paleoenvironmental history of this region. From the more southerly site, Dominion Range, an ~7000-year-long record reveals change in the influence of tropospheric transport to the region. At this site, milder conditions and increased tropospheric inflow prior to ~1500 yr BP are characterized by increased seasalt (ss), terrestrial and marine biogenic inputs. Increased persistence and/or extent of polar stratospheric clouds accompanying generally cooler conditions characterize much of the period since ~1500 yr BP. From the more northerly site, Newall Glacier, the dramatic influence of the retreat of grounded ice from McMurdo Sound dated at[Denton et al., 1989] dominates much of the ice core record. This regional environmental change is documented by massive influxes to the core site of evaporitic salts from areas exposed during low lake level stands. During the past ~150 yr, both Dominion Range and Newall Glacier appear to be experiencing an overall increase in the exposure of ice-free terrain

Aerosol chemical composition and distribution during the Pacific Exploratory Mission (PEM) Tropics

Distributions of aerosol-associated soluble ions over much of the South Pacific were determined by sampling from the NASA DC-8 as part of the Pacific Exploratory Mission (PEM) Tropics campaign. The mixing ratios of all ionic species were surprisingly low throughout the free troposphere (2-12 km), despite the pervasive influence from biomass burning plumes advecting over the South Pacific from the west during PEM-Tropics. At the same time, the specific activity of 7Be frequently exceeded 1000 fCi m-3 through much of the depth of the troposphere. These distributions indicate that the plumes must have been efficiently scavenged by precipitation (removing the soluble ions), but that the scavenging must have occurred far upwind of the DC-8 sampling regions (otherwise 7Be activities would also have been low). This inference is supported by large enhancements of HNO3 and carboxylic acids in many of the plumes, as these soluble acidic gases would also be readily scavenged in any precipitation events. Decreasing mixing ratios of NH4 + with altitude in all South Pacific regions sampled provide support for recent suggestions that oceanic emissions of NH3 constitute a significant source far from continents. Our sampling below 2 km reaffirms the latitudinal pattern in the methylsulfonate/non-sea-salt sulfate (MSA/nss SO4 =) molar ratio established through surface-based and shipboard sampling, with values increasing from \u3c0.05 in the tropics to nearly 0.6 at 70°S. However, we also found very high values of this ratio (0.2-0.5) at 10 km altitude above the intertropical convergence zone near 10°N. It appears that wet convective pumping of dimethylsulfide from the tropical marine boundary layer is responsible for the high values of the MSA/nss SO4 = ratio in the tropical upper troposphere. This finding complicates use of this ratio to infer the zonal origin of biogenic S transported long distances. Copyright 1999 by the American Geophysical Union

Two-hundred-year record of biogenic sulfur in a south Greenland ice core (20D)

The concentration of methanesulfonic acid (MSA) was determined in a shallow south central Greenland ice core(20D). This study provides a high-resolution record of the DMS-derived biogenic sulfur in Greenland precipitation over the past 200 years. The mean concentration of MSA is 3.30 ppb(σ = 2.38 ppb,n = 1134). The general trend of MSA is an increase from 3.01 to 4.10 ppb between 1767 and 1900, followed by a steady decrease to 2.34 ppb at the present time. This trend is in marked contrast to that of non-sea-salt sulfate (nss SO42-), which increases dramatically after 1900 due to the input of anthropogenic sulfur. The MSA fraction ((MSA/(MSA+ nss SO42-))* 100) ranges from a mean of 15% in preindustrial ice to less than 5% in recent ice. These MSA fraction suggest that approximately 5 to 40% of the sulfur in recent Greenland ice is of biological origin. It is suggested that there is a significant low-latitude component to the biogenic sulfur in the core and that variations in the MSA fraction reflect changes in the relative strengths of low- and high-latitude inputs. The data shown o evidence for a strong dependence of dimethyl sulfide(DMS) emissions on sea surface temperature during the last century. There is also no indication that the yield of MSA from DMS oxidation has been altered by increased NOx levels over the North Atlantic during this period

Aerosols in the Pre-industrial Atmosphere

Purpose of Review: We assess the current understanding of the state and behaviour of aerosols under pre-industrial conditions and the importance for climate. Recent Findings: Studies show that the magnitude of anthropogenic aerosol radiative forcing over the industrial period calculated by climate models is strongly affected by the abundance and properties of aerosols in the pre-industrial atmosphere. The low concentration of aerosol particles under relatively pristine conditions means that global mean cloud albedo may have been twice as sensitive to changes in natural aerosol emissions under pre-industrial conditions compared to present-day conditions. Consequently, the discovery of new aerosol formation processes and revisions to aerosol emissions have large effects on simulated historical aerosol radiative forcing. Summary: We review what is known about the microphysical, chemical, and radiative properties of aerosols in the pre-industrial atmosphere and the processes that control them. Aerosol properties were controlled by a combination of natural emissions, modification of the natural emissions by human activities such as land-use change, and anthropogenic emissions from biofuel combustion and early industrial processes. Although aerosol concentrations were lower in the pre-industrial atmosphere than today, model simulations show that relatively high aerosol concentrations could have been maintained over continental regions due to biogenically controlled new particle formation and wildfires. Despite the importance of pre-industrial aerosols for historical climate change, the relevant processes and emissions are given relatively little consideration in climate models, and there have been very few attempts to evaluate them. Consequently, we have very low confidence in the ability of models to simulate the aerosol conditions that form the baseline for historical climate simulations. Nevertheless, it is clear that the 1850s should be regarded as an early industrial reference period, and the aerosol forcing calculated from this period is smaller than the forcing since 1750. Improvements in historical reconstructions of natural and early anthropogenic emissions, exploitation of new Earth system models, and a deeper understanding and evaluation of the controlling processes are key aspects to reducing uncertainties in future

A study of methanesulfonic acid in ice cores

Methanesulfonic acid (MSA), an oxidation product of DMS, is used as a biogenic sulfur tracer in deposited snow layers to better understand the relative importance of various sulfur inputs (biogenic, volcanic and anthropogenic sulfur) to both polar regions in the past.The ice cores and snowpit samples were collected from the 20D site (Greenland) and the Dominion Range site (Antarctica). A suppressed ion chromatographic method was used to measure MSA in snow and ice. The mean concentration of MSA in the 20D ice core is 3.30 ppb ($\sigma$ = 2.38 ppb, n = 1134). The MSA concentrations have decreased since 1900. The ratios of MSA/total S(VI) in the 20D ice core ranged from 15% before 1900 to 5% after 1900. These results suggest a non-biogenic sulfate source to the Greenland ice sheet at the present time. Based on the assumption that the pre-industrial ratios reflect the biogenic sulfur component in the sulfur burden, we estimate that, at the present time, approximately 80% of sulfur input to Greenland is contributed to non-biogenic sulfur.Seasonal variations of MSA in ice are observed in many but not all years. The seasonality in the 20D ice core is consistent with aerosol MSA data from high latitude stations which confirms that ice records that atmospheric changes. Complications of meterological conditions are believed to be responsible for the lack of seasonality of MSA in ice.The mean concentrations of MSA in the Dominion Range snowpit and ice core are 2.76 ppb ($\sigma$ = 2.36, n = 199) and 0.94 ppb ($\sigma$ = 0.56, n = 258), respectively. The mean MSA/total S(VI) ratio is below 1% at the Dominion Range site. These data confirm that the MSA fraction in the high plateau is considerably lower than in coastal Antarctica and in the low- and the high-latitude marine boundary layer. Possible causes include volcanic sulfate input, long range transport of low-latitude biogenic sulfur, and additional stratospheric sulfate input.In summary, all of the above suggest that transport related sulfur source changes may primarily control the atmospheric chemistry, and consequently the ice chemistry, in both polar regions.</p

Methanesulfonate in the Greenland Ice Sheet Project 2 Ice Core

In this paper we present measurements of methanesulfonate in the Greenland Ice Sheet Project 2 (GISP2) ice core. Methanesulfonate is an atmospheric oxidation product of dimethylsulfide. The GISP2 methanesulfonate record contains information about the atmospheric loading of biogenic sulfur over the past 110 kyr and its relationship to climate change. The GISP2 data set supports the inferences made from the Renland ice core from Greenland that the glacial atmosphere over Greenland had reduced concentrations of biogenic sulfur compared with the present day [Hansson and Saltzman, 1993]. We conclude that the flux of biogenic sulfur from the North Atlantic Ocean must have been lower during glacial times and speculate that this decrease may have been related to differences in phytoplankton speciation. The data suggest that changes in direct radiative forcing from biogenic sulfur aerosols would act as negative feedback to the glacial/interglacial climate cycles in this region

Systematic Review: Land Cover, Meteorological, and Socioeconomic Determinants of Aedes Mosquito Habitat for Risk Mapping

Asian tiger and yellow fever mosquitoes (Aedes albopictus and Ae. aegypti) are global nuisances and are competent vectors for viruses such as Chikungunya (CHIKV), Dengue (DV), and Zika (ZIKV). This review aims to analyze available spatiotemporal distribution models of Aedes mosquitoes and their influential factors. A combination of five sets of 3–5 keywords were used to retrieve all relevant published models. Five electronic search databases were used: PubMed, MEDLINE, EMBASE, Scopus, and Google Scholar through 17 May 2017. We generated a hierarchical decision tree for article selection. We identified 21 relevant published studies that highlight different combinations of methodologies, models and influential factors. Only a few studies adopted a comprehensive approach highlighting the interaction between environmental, socioeconomic, meteorological and topographic systems. The selected articles showed inconsistent findings in terms of number and type of influential factors affecting the distribution of Aedes vectors, which is most likely attributed to: (i) limited availability of high-resolution data for physical variables, (ii) variation in sampling methods; Aedes feeding and oviposition behavior; (iii) data collinearity and statistical distribution of observed data. This review highlights the need and sets the stage for a rigorous multi-system modeling approach to improve our knowledge about Aedes presence/abundance within their flight range in response to the interaction between environmental, socioeconomic, and meteorological systems