scholarly journals Natural and anthropogenic variations in atmospheric mercury deposition during the Holocene near Quelccaya Ice Cap, Peru

2014 ◽  
Vol 28 (4) ◽  
pp. 437-450 ◽  
Author(s):  
Samuel A. Beal ◽  
Meredith A. Kelly ◽  
Justin S. Stroup ◽  
Brian P. Jackson ◽  
Thomas V. Lowell ◽  
...  
Keyword(s):  
Atmospheric Mercury ◽  
Mercury Deposition ◽  
The Holocene ◽  
Ice Cap ◽  
Quelccaya Ice Cap

Provenance of basaltic tephra from Vatnajökull subglacial volcanoes, Iceland, as determined by major- and trace-element analyses

The Holocene ◽  
2011 ◽  
Vol 21 (7) ◽  
pp. 1037-1048 ◽  
Author(s):  
Bergrún Arna Óladóttir ◽  
Olgeir Sigmarsson ◽  
Gudrún Larsen ◽  
Jean-Luc Devidal
Keyword(s):  
Trace Element ◽  
Inductively Coupled Plasma ◽  
Major Element ◽  
Element Composition ◽  
Major Element Composition ◽  
Volcanic System ◽  
The Holocene ◽  
Inductively Coupled ◽  
Ice Cap ◽  
The North

The Holocene eruption history of subglacial volcanoes in Iceland is largely recorded by their tephra deposits. The numerous basaltic tephra offer the possibility to make the tephrochronology in the North Atlantic area more detailed and, therefore, more useful as a tool not only in volcanology but also in environmental and archaeological studies. The source of a tephra is established by mapping its distribution or inferred via compositional fingerprinting, mainly based on major-element analyses. In order to improve the provenance determinations for basaltic tephra produced at Grímsvötn, Bárdarbunga and Kverkfjöll volcanic systems in Iceland, 921 samples from soil profiles around the Vatnajökull ice-cap were analysed for major-element concentrations by electron probe microanalysis. These samples are shown to represent 747 primary tephra units. The tephra erupted within each of these volcanic system has similar chemical characteristics. The major-element results fall into three distinctive compositional groups, all of which show regular decrease of MgO with increasing K2O concentrations. The new analyses presented here considerably improve the compositional distinction between products of the three volcanic systems. Nevertheless, slight overlap of the compositional groups for each system still remains. In situ trace-element analyses by laser-ablation-inductively-coupled-plasma-mass-spectrometry were applied for better provenance identification for those tephra having similar major-element composition. Three trace-element ratios, Rb/Y, La/Yb and Sr/Th, proved particularly useful. Significantly higher La/Yb distinguishes the Grímsvötn basalts from those of Bárdarbunga and Rb/Y values differentiate the basalts of Grímsvötn and Kverkfjöll. Additionally, the products of Bárdarbunga, Grímsvötn and Kverkfjöll form distinct compositional fields on a Sr/Th versus Th plot. Taken together, the combined use of major- and trace-element analyses in delineating the provenance of basaltic tephra having similar major-element composition significantly improves the Holocene tephra record as well as the potential for correlations with tephra from outside Iceland.

scholarly journals Glaciological Investigations of the Tropical Quelccaya Ice Cap, Peru

1980 ◽  
Vol 25 (91) ◽  
pp. 69-84 ◽  
Author(s):  
Lonnie G. Thompson
Keyword(s):  
Rainy Season ◽  
Ice Core ◽  
Ice Cores ◽  
Dry Season ◽  
Radioactive Material ◽  
Polar Regions ◽  
Near Surface ◽  
Ice Cap ◽  
Activity Measurements ◽  
Quelccaya Ice Cap

AbstractGlaciological results of the continuing investigations of the Quelccaya ice cap located at lat. 13° 56’ S., long. 70° 50’ W., in the Cordillera Oriental of southern Peru are presented. Ice cores to a depth of 15 m have been retrieved from the summit dome (5650 m), middle dome (5543 m), and south dome (5480 m) and sampled in detail for microparticle, oxygen-isotope, and total-β-activity measurements. Results of these core analyses indicate that although the summit of this ice cap is only 300 m above the annual snow line and the firn is temperate, an interpretable stratigraphic record is preserved. The marked seasonal ice stratigraphy is produced by the marked seasonal variation in regional precipitation. High concentrations of microparticles and β- radioactive material occur during the dry season (May-August). Microparticles deposited during the rainy season are larger than those deposited during the dry season. On the Quelccaya ice cap the most negative δ18O values occur during the warmer rainy season (the opposite occurs in polar regions). The near-surface mean δ value of – 21‰ is remarkably low for this tropical site where the measured mean annual air temperature is – 3°C The seasonality of the microparticles, total β activity, and isotope ratios offers the prospect of a climatic ice-core record from this tropical ice cap.

scholarly journals Characteristics of atmospheric mercury deposition and size-fractionated particulate mercury in urban Nanjing, China

2014 ◽  
Vol 14 (5) ◽  
pp. 2233-2244 ◽  
Author(s):  
J. Zhu ◽  
T. Wang ◽  
R. Talbot ◽  
H. Mao ◽  
X. Yang ◽  
...  
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Fine Particles ◽  
Unit Area ◽  
Atmospheric Mercury ◽  
Anthropogenic Sources ◽  
Deposition Flux ◽  
Coarse Particles ◽  
Mercury Deposition ◽  
Particulate Mercury

Abstract. A comprehensive measurement study of mercury wet deposition and size-fractionated particulate mercury (HgP) concurrent with meteorological variables was conducted from June 2011 to February 2012 to evaluate the characteristics of mercury deposition and particulate mercury in urban Nanjing, China. The volume-weighted mean (VWM) concentration of mercury in rainwater was 52.9 ng L−1 with a range of 46.3–63.6 ng L−1. The wet deposition per unit area was averaged 56.5 μg m−2 over 9 months, which was lower than that in most Chinese cities, but much higher than annual deposition in urban North America and Japan. The wet deposition flux exhibited obvious seasonal variation strongly linked with the amount of precipitation. Wet deposition in summer contributed more than 80% to the total amount. A part of contribution to wet deposition of mercury from anthropogenic sources was evidenced by the association between wet deposition and sulfates, as well as nitrates in rainwater. The ions correlated most significantly with mercury were formate, calcium, and potassium, which suggested that natural sources including vegetation and resuspended soil should be considered as an important factor to affect the wet deposition of mercury in Nanjing. The average HgP concentration was 1.10 ± 0.57 ng m−3. A distinct seasonal distribution of HgP concentrations was found to be higher in winter as a result of an increase in the PM10 concentration. Overall, more than half of the HgP existed in the particle size range less than 2.1 μm. The highest concentration of HgP in coarse particles was observed in summer, while HgP in fine particles dominated in fall and winter. The size distribution of averaged mercury content in particulates was bimodal, with two peaks in the bins of < 0.7 μm and 4.7–5.8 μm. Dry deposition per unit area of HgP was estimated to be 47.2 μg m−2 using meteorological conditions and a size-resolved particle dry deposition model. This was 16.5% less than mercury wet deposition. Compared to HgP in fine particles, HgP in coarse particles contributed more to the total dry deposition due to higher deposition velocities. Negative correlation between precipitation and the HgP concentration reflected the effect of scavenging of HgP by precipitation.

Gaseous mercury in coastal urban areas

2010 ◽  
Vol 7 (6) ◽  
pp. 537 ◽  
Author(s):  
Anne L. Soerensen ◽  
Henrik Skov ◽  
Matthew S. Johnson ◽  
Marianne Glasius
Keyword(s):  
Urban Areas ◽  
Marine Boundary Layer ◽  
Elemental Mercury ◽  
Atmospheric Mercury ◽  
Mercury Deposition ◽  
Mercury Emissions ◽  
Gaseous Elemental Mercury ◽  
Gaseous Mercury ◽  
Range Transport ◽  
Aquatic Food

Environmental context Mercury is a neurotoxin that bioaccumulates in the aquatic food web. Atmospheric emissions from urban areas close to the coast could cause increased local mercury deposition to the ocean. Our study adds important new data to the current limited knowledge on atmospheric mercury emissions and dynamics in coastal urban areas. Abstract Approximately 50% of primary atmospheric mercury emissions are anthropogenic, resulting from e.g. emission hotspots in urban areas. Emissions from urban areas close to the coast are of interest because they could increase deposition loads to nearby coastal waters as well as contribute to long range transport of mercury. We present results from measurements of gaseous elemental mercury (GEM) and reactive gaseous mercury (RGM) in 15 coastal cities and their surrounding marine boundary layer (MBL). An increase of 15–90% in GEM concentration in coastal urban areas was observed compared with the remote MBL. Strong RGM enhancements were only found in two cities. In urban areas with statistically significant GEM/CO enhancement ratios, slopes between 0.0020 and 0.0087 ng m–3 ppb–1 were observed, which is consistent with other observations of anthropogenic enhancement. The emission ratios were used to estimate GEM emissions from the areas. A closer examination of data from Sydney (Australia), the coast of Chile, and Valparaiso region (Chile) in the southern hemisphere, is presented.

scholarly journals The Glaciochemistry of Snow-Pits from Quelccaya Ice Cap, Peru, 1982

1985 ◽  
Vol 7 ◽  
pp. 84-88 ◽  
Author(s):  
W. Berry Lyons ◽  
A. Paul Mayewski ◽  
Lonnie G. Thompson ◽  
Boyd Allen
Keyword(s):  
Amazon Basin ◽  
Atomic Absorption Spectrophotometry ◽  
High Elevation ◽  
Common Source ◽  
Gaseous Emissions ◽  
Polar Ice ◽  
Peruvian Andes ◽  
Reactive Iron ◽  
Ice Cap ◽  
Quelccaya Ice Cap

We present glaciochemical data from a pilot study of two snow-pits from Quelccaya ice cap, Peruvian Andes. These are the first samples to be analyzed from Quelccaya for nitrate and sulfate by ion chromatography (IC), for nitrate-plus-nitrite, reactive silicate and reactive iron by colorimetry, and for sodium by atomic absorption spectrophotometry. The 3 m pits used in this study represent a one year record of mass accumulation and the 29 samples collected provide the first glaciochemical data from this area which can be compared with glaciochemical studies from other locations.Reactive iron, reactive silicate and sodium, and the profiles of >0.63μm microparticles from Thompson and others (1984) are coincident, suggesting that transport and deposition into this area of each species are controlled by similar processes. The common source is probably local, resulting from crustal weathering. In general, the reactive silicate values are lower than those observed in other alpine glacier ice. The highest sulfate and nitrate values were observed in the upper few centimeters of the snow-pit. Most of the sulfate concentrations were less than 3 μM and are similar to values obtained for fresh surface snows from Bolivia (Stallard and Edmond 1981). Since biological gaseous emissions are thought to be the major source of sulfur and nitrogen to the atmosphere over the Amazon basin, the sulfate and nitrate fluctuations may be due to seasonal biological input and/or seasonal shifts in wind direction bringing material to Quelccaya.With only one exception, the colorimetric nitrate-plus-nitrite data were higher than the IC nitrate data. Unfortunately, the IC analyses were conducted 81 d after the colorimetric analyses. The difference between the two data sets could be attributable to the following: (1) the colorimetric technique may yield erroneously high results as suggested for polar ice by Herron (1982), (2) the IC technique yields erroneously low results due, in part, to the possible exclusion of nitrite concentrations, and/or (3) nitrite was lost via biological removal during the 81 d period before the IC analyses. If the IC data are correct, the mean nitrate value is 0.4μΜ (n = 29). This value is similar to those reported from pre-industrial aged polar ice (Herron 1982). If the colorimetric mean value (1.1 μM) is correct, it is similar to colorimetrically determined values from other high-elevation alpine ice (Lyons and Mayewski 1983).

scholarly journals Thinning of the Quelccaya Ice Cap over the last thirty years

2016 ◽  
Author(s):  
C. D. Chadwell ◽  
D. R. Hardy ◽  
C. Braun ◽  
H. H. Brecher ◽  
L. G. Thompson
Keyword(s):  
Unit Volume ◽  
Environmental Changes ◽  
Statistical Significance ◽  
Geophysical Methods ◽  
Snow Accumulation ◽  
Dual Frequency ◽  
The Past ◽  
Ice Cap ◽  
Ice Surface ◽  
Quelccaya Ice Cap

Abstract. Direct measurements of the decadal response of Tropical glaciers to environmental changes are difficult to acquire within their accumulation zones. In 2013, we used dual-frequency kinematic GPS to re-measure the surface elevations at 46 sites, from the margin to across the summit of the Quelccaya Ice Cap, first measured in 1983 using terrestrial surveying methods. In 2015, six additional sites on the western margin, first observed in 1978, were remeasured. Over the past 30 years, the ice cap summit has thinned by 4.41 &amp;pm; 0.23 m (2σ), with a maximum ice loss at one site near the margin of 63.4 &amp;pm; 0.34 m (2σ) over 37 years. Using geophysical methods that located the sub-glacial bedrock, we estimate the unit-volume of ice in 1983 along a profile from the 1983 margin to the summit and then the change in volume from 1983 to 2013 by differencing the surface elevations. Over the past 30 years, 21.2 &amp;pm; 0.3 % (2σ) of the ice unit-volume has been lost suggesting an average annual mass balance rate of −0.5 &amp;pm; 0.1 m w.e. a−1 (2σ). Increasing air temperature at high elevations of the Andes is likely a major driver of the observed changes. Specifically, within the ablation zone, thinning is likely caused by a 1–2 m w.e. a−1 increase in melting and sublimation above steady-state.Within the accumulation zone, analysis of annual, dry-season summit pits suggests that surface lowering may be caused by both a slight decrease in net snow accumulation and an increase in firnification rate, though this interpretation yet lacks statistical significance. The role of ice flux changes since 1983/4 remains unconstrained, awaiting updated measurements of ice surface velocities across the ice cap.

scholarly journals Model analyses of atmospheric mercury: present air quality and effects of transpacific transport on the United States

2013 ◽  
Vol 13 (4) ◽  
pp. 9849-9893 ◽  
Author(s):  
H. Lei ◽  
X.-Z. Liang ◽  
D. J. Wuebbles ◽  
Z. Tao
Keyword(s):  
United States ◽  
Air Quality ◽  
Wet Deposition ◽  
Total Mercury ◽  
The United States ◽  
Atmospheric Mercury ◽  
Anthropogenic Sources ◽  
Mercury Deposition ◽  
Transpacific Transport ◽  
Mercury Cycle

Abstract. Atmospheric mercury is a toxic air and water pollutant that is of significant concern because of its effects on human health and ecosystems. A mechanistic representation of the atmospheric mercury cycle is developed for the state-of-the-art global climate-chemistry model, CAM-Chem (Community Atmospheric Model with Chemistry). The model simulates the emission, transport, transformation and deposition of atmospheric mercury (Hg) in three forms: elemental mercury (Hg(0)), reactive mercury (Hg(II)), and particulate mercury (PHg). Emissions of mercury include those from human, land, ocean, biomass burning and volcano related sources. Land emissions are calculated based on surface solar radiation flux and skin temperature. A simplified air–sea mercury exchange scheme is used to calculate emissions from the oceans. The chemistry mechanism includes the oxidation of Hg(0) in gaseous phase by ozone with temperature dependence, OH, H2O2 and chlorine. Aqueous chemistry includes both oxidation and reduction of Hg(0). Transport and deposition of mercury species are calculated through adapting the original formulations in CAM-Chem. The CAM-Chem model with mercury is driven by present meteorology to simulate the present mercury air quality during the 1999–2001 periods. The resulting surface concentrations of total gaseous mercury (TGM) are then compared with the observations from worldwide sites. Simulated wet depositions of mercury over the continental United States are compared to the observations from 26 Mercury Deposition Network stations to test the wet deposition simulations. The evaluations of gaseous concentrations and wet deposition confirm a strong capability for the CAM-Chem mercury mechanism to simulate the atmospheric mercury cycle. The results also indicate that mercury pollution in East Asia and Southern Africa is very significant with TGM concentrations above 3.0 ng m−3. The comparison to wet deposition indicates that wet deposition patterns of mercury are more affected by the spatial variability of precipitation. The sensitivity experiments show that 22% of total mercury deposition and 25% of TGM concentrations in the United States are resulted from domestic anthropogenic sources, but only 9% of total mercury deposition and 7% of TGM concentrations are contributed by transpacific transport. However, the contributions of domestic and transpacific sources on the western United States levels of mercury are of comparable magnitude.

scholarly journals Atmospheric mercury deposition over the land surfaces and the associated uncertainties in observations and simulations: a critical review

2019 ◽  
Vol 19 (24) ◽  
pp. 15587-15608 ◽  
Author(s):  
Lei Zhang ◽  
Peisheng Zhou ◽  
Shuzhen Cao ◽  
Yu Zhao
Keyword(s):  
Dry Deposition ◽  
Wet Deposition ◽  
Quantitative Methods ◽  
Experimental System ◽  
Elemental Mercury ◽  
Atmospheric Mercury ◽  
Future Research ◽  
Observation Data ◽  
Mercury Deposition ◽  
Land Surfaces

Abstract. One of the most important processes in the global mercury (Hg) biogeochemical cycling is the deposition of atmospheric Hg, including gaseous elemental mercury (GEM), gaseous oxidized mercury (GOM), and particulate-bound mercury (PBM), to the land surfaces. Results of wet, dry, and forest Hg deposition from global observation networks, individual monitoring studies, and observation-based simulations have been reviewed in this study. Uncertainties in the observation and simulation of global speciated atmospheric Hg deposition to the land surfaces have been systemically estimated based on assessment of commonly used observation methods, campaign results for comparison of different methods, model evaluation with observation data, and sensitivity analysis for model parameterization. The uncertainties of GOM and PBM dry deposition measurements come from the interference of unwanted Hg forms or incomplete capture of targeted Hg forms, while that of GEM dry deposition observation originates from the lack of a standardized experimental system and operating procedure. The large biases in the measurements of GOM and PBM concentrations and the high sensitivities of key parameters in resistance models lead to high uncertainties in GOM and PBM dry deposition simulation. Non-precipitation Hg wet deposition could play a crucial role in alpine and coastal regions, and its high uncertainties in both observation and simulation affect the overall uncertainties of Hg wet deposition. The overall uncertainties in the observation and simulation of the total global Hg deposition were estimated to be ± (25–50) % and ± (45–70) %, respectively, with the largest contributions from dry deposition. According to the results from uncertainty analysis, future research needs were recommended, among which a global Hg dry deposition network, unified methods for GOM and PBM dry deposition measurements, quantitative methods for GOM speciation, campaigns for comprehensive forest Hg behavior, and more efforts in long-term Hg deposition monitoring in Asia are the top priorities.

Sign in / Sign up

Export Citation Format

Share Document