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USGS2015

Spatial patterns of atmospheric deposition of nitrogen and sulfur using ion-exchange resin collectors in Rocky Mountain National Park, USA

Lakes and streams in Class 1 wilderness areas in the western United States (U.S.) are at risk from atmospheric deposition of nitrogen (N) and sulfur (S), and protection of these resources is mandated under the Federal Clean Air Act and amendments. Assessment of critical loads, which are the maximum exposure to pollution an area can receive without adverse effects on sensitive ecosystems, requires accurate deposition estimates. However, deposition is difficult and expensive to measure in high-elevation wilderness, and spatial patterns in N and S deposition in these areas remain poorly quantified. In this study, ion-exchange resin (IER) collectors were used to measure dissolved inorganic N (DIN) and S deposition during June 2006–September 2007 at approximately 20 alpine/subalpine sites spanning the Continental Divide in Rocky Mountain National Park. Results indicated good agreement between deposition estimated from IER collectors and commonly used wet + dry methods during summer, but poor agreement during winter. Snowpack sampling was found to be a more accurate way of quantifying DIN and S deposition during winter. Summer DIN deposition was significantly greater on the east side of the park than on the west side (25–50%; p ≤ 0.03), consistent with transport of pollutants to the park from urban and agricultural areas to the east. Sources of atmospheric nitrate (NO 3 − ) were examined using N isotopes. The average δ 15 N of NO 3 − from IER collectors was 3.5&permil; higher during winter than during summer ( p < 0.001), indicating a seasonal shift in the relative importance of regional NO x sources, such as coal combustion and vehicular sources of atmospheric NO 3 − . There were no significant differences in δ 15 N of NO 3 − between east and west sides of the park during summer or winter ( p = 0.83), indicating that the two areas may have similar sources of atmospheric NO 3 − . Results from this study indicate that a combination of IER collectors and snowpack sampling can be used to characterize spatial variability in DIN and S deposition in high-elevation wilderness areas. These data can improve our ability to model critical loads by filling gaps in geographic coverage of deposition monitoring/modeling programs and thus may enable policy makers to better protect sensitive natural resources in Class 1 Wilderness areas.

Colorado↗

USGS2018

Spatial patterns and temporal changes in atmospheric-mercury deposition for the midwestern USA, 2001–2016

Spatial patterns and temporal changes in atmospheric-mercury (Hg) deposition were examined in a five-state study area in the Midwestern USA where 32% of the stationary sources of anthropogenic Hg emissions in the continental USA were located. An extensive monitoring record for wet and dry Hg deposition was compiled for 2001–2016, including 4666 weekly precipitation samples at 13 sites and 27 annual litterfall-Hg samples at 7 sites. This study is the first to examine these Hg data for the Midwestern USA. The median annual precipitation-Hg deposition at the study sites was 10.4 micrograms per square meter per year (ug/m2/year) and ranged from 5.8 ug/m2/year to 15.0 ug/m2/year. The median annual Hg concentration was 9.4 ng/L. Annual litterfall-Hg deposition had a median of 16.1 ug/m2/year and ranged from 9.7 to 23.4 ug/m2/year. Isopleth maps of annual precipitation-Hg deposition indicated a recurring spatial pattern similar to one revealed by statistical analysis of weekly precipitation-Hg deposition. In that pattern, high Hg deposition in southeastern Indiana was present each year, frequently extending to southern Illinois. Most of central Indiana and central Illinois had similar Hg deposition. Areas with comparatively lower annual Hg deposition were observed in Michigan and Ohio for many years and frequently included part of northern Indiana. The area in southern Indiana where high Hg deposition predominated had the highest number of extreme episodes of weekly Hg deposition delivering up to 15% of the annual Hg load from precipitation in a single week. Modeled 48-h back trajectories indicated air masses for these episodes often arrived from the south and southwest, crossing numerous stationary sources of Hg emissions releasing from 23 to more than 300 kg Hg per year. This analysis suggests that local and regional, rather than exclusively continental or global Hg emissions were likely contributing to the extreme episodes and at least in part, to the spatial patterns of precipitation-Hg deposition in the study area. Statistically significant temporal decreases in weekly precipitation-Hg concentrations in the study area between the periods 2001–2013 and 2014–2016 were observed, coinciding with reported reductions in Hg emissions in the USA required by implementation of national Hg emissions-control rules. These decreases in atmospheric-Hg concentrations are believed to have resulted in the reduced atmospheric-Hg deposition recorded because precipitation depths between the two periods were not significantly different. The Hg-monitoring data for the study area identified an atmospheric deposition response to decreased local and regional Hg emissions.

Illinois, Indiana, Kentucky, Michigan, Ohio↗

USGS2016

Assessing atmospheric concentration of polychlorinated biphenyls (PCBs) by evergreen Rhododendron maximum next to a contaminated stream

Conifers are often used as an “air passive sampler”, but few studies have focused on the implication of broadleaf evergreens to monitor atmospheric semivolatile organic compounds such as polychlorinated biphenyls (PCBs). In this study, we used Rhododendron maximum (rhododendron) growing next to a contaminated stream to assess atmospheric PCB concentrations. The study area was located in a rural setting and approximately 2 km downstream of a former Sangamo-Weston (S-W) plant. Leaves from the same mature shrubs were collected in late fall 2010, and winter and spring 2011. PCBs were detected in the collected leaves suggesting that rhododendron can be used as air passive samplers in rural areas where active sampling is impractical. Estimated ΣPCB (47 congeners) concentrations in the atmosphere decreased from fall 2010 to spring 2011 with concentration means at 3990, 2850, and 931 pg m -3 in fall 2010, winter 2011, and spring 2011, respectively. These results indicate that the atmospheric concentrations at this location continue to be high despite termination of active discharge from the former S-W plant. Leaves had a consistent pattern of high concentrations of tetra- and penta-CBs similar to the congener distribution in polyethylene (PE) passive samplers deployed in the water column suggesting that volatilized PCBs from the stream were the primary source of contaminants in rhododendron leaves.

South Carolina↗

USGS2018

Linking transit times to catchment sensitivity to atmospheric deposition of acidity and nitrogen in mountains of the western United States

Transit times are hypothesized to influence catchment sensitivity to atmospheric deposition of acidity and nitrogen (N) because they help determine the amount of time available for infiltrating precipitation to interact with catchment soil and biota. Transit time metrics, including fraction of young water ( F yw ) and mean transit time (MTT), were calculated for 11 headwater catchments in mountains of the western United States based on differences in the amplitude of the seasonal signal of δ 18 O in streamflow and precipitation. Results were statistically compared with catchment characteristics to elucidate controlling mechanisms. Transit times also were compared with stream solute concentrations to test the hypothesis that transit times are a primary influence on weathering rates and biological assimilation of atmospherically deposited N. Results indicate that transit times in the study catchments are strongly related to soil, vegetation, and topographic characteristics, with barren terrain (bare rock and talus) and steep slopes linked to high F yw and short MTT, whereas forest soil (hydrogroup B) was linked to low F yw and greater MTT. Concentrations of silicate weathering products (Na + and Si) were negatively related to F yw and barren terrain, and positively related to MTT and forest soil, supporting the concept that weathering fluxes and buffering capacity tend to be low in alpine areas due to short transit times. Nitrate concentrations were positively related to N deposition, catchment slope, and barren terrain, and negatively related to forest, indicating that hydrologic and/or biogeochemical processes associated with steep slopes limit uptake of atmospherically deposited N by biota. Interannual and seasonal variability in transit times and source water contributions in the study catchments was substantial, reflecting the influence of strong temporal variations in snowmelt inputs in high‐elevation catchments of the western United States. Results from this study confirm that short transit times in these areas are a key reason they are highly sensitive to atmospheric pollution and climate change.

Hydrological Processes↗

USGS2021

The concept of evanescent microbial ecosystems in Earth's atmosphere

This essay presents the hypothesis that short-lived or evanescent microbial ecosystems exist in Earth’s lower troposphere (~ < 4 km). This hypothesis is supported by culture- and molecular-based studies that have shown diverse, viable, and metabolically active microbial communities within Earth’s atmospheric boundary layer. Surprisingly, microorganisms are routinely recovered in samples collected at extreme altitudes including those within the stratosphere (> 18 km). Volcanic eruptions, dust storms, fires, and sea spray are known to seed the atmosphere with microorganisms and to serve as potential nutrient sources while in the atmosphere and upon deposition. Recent research has demonstrated that microorganisms are metabolically active in clouds; for example, archaea capable of utilizing gases such as methane and hydrogen-nitrogen have been identified in clouds and in the atmosphere over natural and anthropogenic gas seeps. The only difference between this hypothesized ecosystem to more traditionally defined ecosystems is its evanescent characteristics where clouds or gas plumes eventually dissipate as they reside over and traverse Earth’s terrestrial and/or aquatic environments. The life cycle of these hypothesized evanescent airborne ecosystems would be short-lived relative to the classically defined biomes or ecosystems.

Book chapter↗

USGS2019

Isotopic evidence that nitrogen enrichment intensifies nitrogen losses to the atmosphere from subtropical mangroves

Nitrogen (N) enrichment can have large effects on mangroves’ capacity to provide critical ecosystem services by affecting fundamental functions such as N cycling and primary productivity. However, our understanding of excess N input effects on N cycling in mangroves remains quite limited. To advance our understanding of how N enrichment via water or air pollution affects mangroves, we evaluated whether increasing N inputs would decrease biological N fixation (BNF), but intensify N dynamics and N losses to the atmosphere in these systems. We measured N concentrations in sediment and vegetation, rates of BNF in sediment and litter, and net sediment ammonification and nitrification rates. We also evaluated long-term integrated N dynamics and N losses to the atmosphere using the natural abundance of N stable isotopes (δ 15 N) in the sediment–plant system and in estuarine water. We performed these analyses at non-N-enriched and N-enriched (that is, polluted) fringe and basin mangroves in southeastern Brazil. The δ 15 N in the sediment–plant system was higher at N-enriched than non-N-enriched fringe sites, indicating increased N losses to the atmosphere from N-enriched sites. However, N concentrations in sediment and vegetation were similar or lower at N-enriched relative to non-N-enriched sites. BNF and net ammonification and nitrification rates were also similar between N-enriched and non-N-enriched sites. Excess N inputs intensified N losses to the atmosphere from mangroves, but N pools, BNF, and net ammonification and nitrification rates were not affected by N enrichment, likely because excess N was quickly lost from the system by direct denitrification and volatilization.

São Paulo↗

USGS2009

Compositional changes in sediments of subalpine lakes, Uinta Mountains (Utah): Evidence for the effects of human activity on atmospheric dust inputs

Sediments in Marshall and Hidden Lakes in the Uinta Mountains of northeastern Utah contain records of atmospheric mineral-dust deposition as revealed by differences in mineralogy and geochemistry of lake sediments relative to Precambrian clastic rocks in the watersheds. In cores spanning more than a thousand years, the largest changes in composition occurred within the past approximately 140 years. Many elements associated with ore deposits (Ag, As, Bi, Cd, Cu, In, Mo, Pb, S, Sb, Sn, and Te) increase in the lake sediments above depths that correspond to about AD 1870. Sources of these metals from mining districts to the west of the Uinta Mountains are suggested by (1) the absence of mining and smelting of these metals in the Uinta Mountains, and (2) lower concentrations of most of these elements in post-settlement sediments of Hidden Lake than in those of Marshall Lake, which is closer to areas of mining and the densely urbanized part of north-central Utah that is termed the Wasatch Front, and (3) correspondence of Pb isotopic compositions in the sediments with isotopic composition of ores likely to have been smelted in the Wasatch Front. A major source of Cu in lake sediments may have been the Bingham Canyon open-pit mine 110 km west of Marshall Lake. Numerous other sources of metals beyond the Wasatch Front are likely, on the basis of the widespread increases of industrial activities in western United States since about AD 1900. In sediment deposited since ca. AD 1945, as estimated using 239+240 Pu activities, increases in concentrations of Mn, Fe, S, and some other redox-sensitive metals may result partly from diagenesis related to changes in redox. However, our results indicate that these elemental increases are also related to atmospheric inputs on the basis of their large increases that are nearly coincident with abrupt increases in silt-sized, titanium-bearing detrital magnetite. Such magnetite is interpreted as a component of atmospheric dust, because it is absent in catchment bedrock. Enrichment of P in sediments deposited after ca. AD 1950 appears to be caused largely by atmospheric inputs, perhaps from agricultural fertilizer along with magnetite-bearing soil.

Utah↗

USGS2005

The atmospheres of Saturn and Titan in the near-infrared: First results of Cassini/Vims

The wide spectral coverage and extensive spatial, temporal, and phase-angle mapping capabilities of the Visual Infrared Mapping Spectrometer (VIMS) onboard the Cassini-Huygens Orbiter are producing fundamental new insights into the nature of the atmospheres of Saturn and Titan. For both bodies, VIMS maps over time and solar phase angles provide information for a multitude of atmospheric constituents and aerosol layers, providing new insights into atmospheric structure and dynamical and chemical processes. For Saturn, salient early results include evidence for phosphine depletion in relatively dark and less cloudy belts at temperate and mid-latitudes compared to the relatively bright and cloudier Equatorial Region, consistent with traditional theories of belts being regions of relative downwelling. Additional Saturn results include (1) the mapping of enhanced trace gas absorptions at the south pole, and (2) the first high phase-angle, high-spatial-resolution imagery of CH4 fluorescence. An additional fundamental new result is the first nighttime near-infrared mapping of Saturn, clearly showing discrete meteorological features relatively deep in the atmosphere beneath the planet's sunlit haze and cloud layers, thus revealing a new dynamical regime at depth where vertical dynamics is relatively more important than zonal dynamics in determining cloud morphology. Zonal wind measurements at deeper levels than previously available are achieved by tracking these features over multiple days, thereby providing measurements of zonal wind shears within Saturn's troposphere when compared to cloudtop movements measured in reflected sunlight. For Titan, initial results include (1) the first detection and mapping of thermal emission spectra of CO, CO2, and CH3D on Titan's nightside limb, (2) the mapping of CH4 fluorescence over the dayside bright limb, extending to ??? 750 km altitude, (3) wind measurements of ???0.5 ms-1, favoring prograde, from the movement of a persistent (multiple months) south polar cloud near 88??S latitude, and (4) the imaging of two transient mid-southern-latitude cloud features. ?? Springer Science+Business Media, Inc. 2006.

Earth, Moon and Planets↗

USGS2019

AVO-G2S: A modified, open-source Ground-to-Space atmospheric specification for infrasound modeling

To facilitate infrasound propagation studies, we present AVO-G2S, an open-source, Ground-to-Space model which provides temperature and wind specifications from the surface to an altitude of 225 km. This model provides a means of smoothly characterizing atmospheric conditions using multiple numerical weather prediction forecast and reanalysis products, along with upper-atmospheric empirical models. Regional atmospheric reconstructions only require a limited domain and can utilize high-resolution numerical weather prediction forecasts typically provided on a projected grid. The use of a projected grid allows for faster spectral transform libraries to be employed. The AVO-G2S software can also provide global reconstructions that rely on global numerical weather prediction products and spherical harmonic decompositions. AVO-G2S is inspired by a global Ground-to-Space model developed by the Naval Research Laboratory, and relies on their empirical descriptions of upper-atmospheric conditions. Alaska Volcano Observatory has implemented this model for near-real-time infrasound monitoring of volcanic eruptions and historical research projects.

Computers & Geosciences↗

USGS2004

Historical trends in occurrence and atmospheric inputs of halogenated volatile organic compounds in untreated ground water used as a source of drinking water

Analyses of samples of untreated ground water from 413 community-, non-community- (such as restaurants), and domestic-supply wells throughout the US were used to determine the frequency of detection of halogenated volatile organic compounds (VOCs) in drinking-water sources. The VOC data were compiled from archived chromatograms of samples analyzed originally for chlorofluorocarbons (CFCs) by purge-and-trap gas chromatography with an electron-capture detector (GC-ECD). Concentrations of the VOCs could not be ascertained because standards were not routinely analyzed for VOCs other than trichloromonofluoromethane (CFC-11), dichlorodifluoromethane (CFC-12) and 1,1,2-trichloro-1,2,2-trifluoroethane (CFC-113). Nevertheless, the peak areas associated with the elution times of other VOCs on the chromatograms can be classified qualitatively to assess concentrations at a detection limit on the order of parts per quadrillion. Three or more VOCs were detected in 100% (percent) of the chromatograms, and 77.2% of the samples contained 10 or more VOCs. The maximum number of VOCs detected in any sample was 24. Modeled ground-water residence times, determined from concentrations of CFC-12, were used to assess historical trends in the cumulative occurrence of all VOCs detected in this analysis, as well as the occurrence of individual VOCs, such as CFC-11, carbon tetrachloride (CCl 4 ), chloroform and tetrachloroethene (PCE). The detection frequency for all of the VOCs detected has remained relatively constant from approximately 1940 to 2000; however, the magnitude of the peak areas on the chromatograms for the VOCs in the water samples has increased from 1940 to 2000. For CFC-11, CCl 4 , chloroform and PCE, small peaks decrease from 1940 to 2000, and large peaks increase from 1940 to 2000. The increase in peak areas on the chromatograms from analyses of more recently recharged water is consistent with reported increases in atmospheric concentrations of the VOCs. Approximately 44% and 6.7% of the CCl 4 and PCE detections, respectively, in pre-1940 water, and 68% and 62% of the CCl 4 and PCE detections, respectively, in water recharged in 2000 exceed solubility equilibrium with average atmospheric concentrations. These exceedences can be attributed to local atmospheric enrichment or direct contaminant input to ground-water flow systems. The detection of VOCs at concentrations indicative of atmospheric sources in 100% of the samples indicates that untreated drinking water from ground-water sources in the US recharged within the past 60 years has been affected by anthropogenic activity. Additional inputs from a variety of sources such as spills, underground injections and leaking landfills or storage tanks increasingly are providing additional sources of contamination to ground water used as drinking-water sources.

Science of the Total Environment↗

USGS2006

Atmospheric mercury speciation in Yellowstone National Park

Atmospheric concentrations of elemental mercury (Hg 0 ), reactive gaseous Hg (RGM), and particulate Hg (pHg) concentrations were measured in Yellowstone National Park (YNP), U.S.A. using high resolution, real time atmospheric mercury analyzers (Tekran 2537A, 1130, and 1135). A survey of Hg 0 concentrations at various locations within YNP showed that concentrations generally reflect global background concentrations of 1.5–2.0 ng m − 3 , but a few specific locations associated with concentrated geothermal activity showed distinctly elevated Hg 0 concentrations (about 9.0 ng m − 3 ). At the site of intensive study located centrally in YNP (Canyon Village), Hg 0 concentrations did not exceed 2.5 ng m − 3 ; concentrations of RGM were generally below detection limits of 0.88 pg m − 3 and never exceeded 5 pg m − 3 . Concentrations of pHg ranged from below detection limits to close to 30 pg m −3 . RGM and pHg concentrations were not correlated with any criteria gases (SO 2 , NO x , O 3 ); however pHg was weakly correlated with the concentration of atmospheric particles. We investigated three likely sources of Hg at the intensive monitoring site: numerous geothermal features scattered throughout YNP, re-suspended soils, and wildfires near or in YNP. We examined relationships between the chemical properties of aerosols (as measured using real time, single particle mass spectrometry; aerosol time-of-flight mass spectrometer; ATOFMS) and concentrations of atmospheric pHg. Based on the presence of particles with distinct chemical signatures of the wildfires, and the absence of signatures associated with the other sources, we concluded that wildfires in the park were the main source of aerosols and associated pHg to our sampling site.

Science of the Total Environment↗

USGS1983

Additions of nutrients and major ions by the atmosphere and tributaries to nearshore waters of northwestern Lake Huron

Nutrient additions by the atmosphere and six tributaries to nearshore waters of northwestern Lake Huron were measured at weekly intervals from August 1975 to July 1976. The atmosphere contributed 43% of the nitrogen (N) and 10% of the phosphorus (P) that was added during the year. The 1975–76 atmospheric loading rate of total N to this area (11 kg/ha/yr) was one of the highest found to date in the United States. N was conserved more efficiently than P in the tributary drainage basins. Of the N and P that fell annually on the watersheds under study, 2 to 37% of the N and 31 to 84% of the P was carried with runoff to the lake. From a basin where ditching and clear-cutting occurred, water, P, silica (SiO 2 ), N, and sodium were lost at higher rates than from five other basins. Most of the N in bulk atmospheric samples (23%) and tributary waters (56%) was dissolved organic N, a form of N not often measured.

Michigan↗

USGS2014

Decreased atmospheric sulfur deposition across the southeastern U.S.: When will watersheds release stored sulfate?

Emissions of sulfur dioxide (SO 2 ) to the atmosphere lead to atmospheric deposition of sulfate (SO 4 2- ), which is the dominant strong acid anion causing acidification of surface waters and soils in the eastern United States (U.S.). Since passage of the Clean Air Act and its Amendments, atmospheric deposition of SO 2 in this region has declined by over 80%, but few corresponding decreases in stream-water SO 4 2- concentrations have been observed in unglaciated watersheds. We calculated SO 4 2- mass balances for 27 forested, unglaciated watersheds from Pennsylvania to Georgia, by using total atmospheric deposition (wet plus dry) as input. Many of these watersheds still retain SO 4 2- , unlike their counterparts in the northeastern U.S. and southern Canada. Our analysis showed that many of these watersheds should convert from retaining to releasing SO 4 2- over the next two decades. The specific years when the watersheds crossover from retaining to releasing SO 4 2- correspond to a general geographical pattern of later net watershed release from north to south. The single most important variable that explained the crossover year was the runoff ratio, defined as the ratio of annual mean stream discharge to precipitation. Percent clay content and mean soil depth were secondary factors in predicting crossover year. The conversion of watersheds from net SO 4 2- retention to release anticipates more widespread reductions in stream-water SO 4 2- concentrations in this region.

Environmental Science & Technology↗

USGS2001

African desert dust in the Caribbean atmosphere: Microbiology and public health

Air samples collected on St. John in the U.S. Virgin Islands were screened for the presence of viable bacteria and fungi to determine if the number of cultivatable microbes in the atmosphere differed between "clear atmospheric conditions" and "African dust-events." Results indicate that during "African dust-events," the numbers of cultivatable airborne microorganisms can be 2 to 3 times that found during "clear atmospheric conditions." Direct microbial counts of air samples using an epifluorescent microscopy assay demonstrated that during an "African dust-event," bacteria-like and virus-like particle counts were approximately one log greater than during "clear atmospheric conditions." Bacteria-like particles exhibiting autofluoresence, a trait of phototrophs, were only detected during an "African dust-event.".

Aerobiologia↗

USGS2011

Exploring Martian polar atmospheric circulation and surface interactions

The northern and southern seasonal polar caps of Mars are formed in the polar night, during their respective autumn and winter seasons, by the condensation of atmospheric CO 2 directly to the solid phase as ice, snow, and possibly frost. During spring and summer, the seasonal ice sublimes, returning CO 2 to the atmosphere. The caps advance and recede in response to seasonal variations in solar insolation, extending as far as 40° from the poles, and have been noted by telescopic observers since the 17th century Roughly 25% of the atmosphere, which is 95% CO 2 by volume, is cycled into and out of the seasonal caps. The CO 2 cycle dominates atmospheric circulation on Mars, and must be thoroughly understood in order to answer fundamental questions about climate history and the global distribution of near‐surface water.

Eos, Transactions, American Geophysical Union↗

USGS2008

Climatically driven loss of calcium in steppe soil as a sink for atmospheric carbon

During the last several thousand years the semi-arid, cold climate of the Russian steppe formed highly fertile soils rich in organic carbon and calcium (classified as Chernozems in the Russian system). Analysis of archived soil samples collected in Kemannaya Steppe Preserve in 1920, 1947, 1970, and fresh samples collected in 1998 indicated that the native steppe Chernozems, however, lost 17-28 kg m-2 of calcium in the form of carbonates in 1970-1998. Here we demonstrate that the loss of calcium was caused by fundamental shift in the steppe hydrologic balance. Previously unleached soils where precipitation was less than potential evapotranspiration are now being leached due to increased precipitation and, possibly, due to decreased actual evapotranspiration. Because this region receives low levels of acidic deposition, the dissolution of carbonates involves the consumption of atmospheric CO2. Our estimates indicate that this climatically driven terrestrial sink of atmospheric CO2 is ???2.1-7.4 g C m-2 a-1. In addition to the net sink of atmospheric carbon, leaching of pedogenic carbonates significantly amplified seasonal amplitude of CO2 exchange between atmosphere and steppe soil. Copyright 2008 by the American Geophysical Union.

Global Biogeochemical Cycles↗

USGS2007

Atmospheric bromine flux from the coastal Abu Dhabi sabkhat: A ground-water mass-balance investigation

A solute mass-balance study of ground water of the 3000 km2 coastal sabkhat (salt flats) of the Emirate of Abu Dhabi, United Arab Emirates, documents an annual bromide loss of approximately 255 metric tons (0.0032 Gmoles), or 85 kg/km2. This value is an order of magnitude greater than previously published direct measurements from the atmosphere over an evaporative environment of a salar in Bolivia. Laboratory evidence, consistent with published reports, suggests that this loss is by vapor transport to the atmosphere. If this bromine flux to the atmosphere is representative of the total earth area of active salt flats then it is a significant, and generally under recognized, input to the global atmospheric bromide flux.

Geophysical Research Letters↗

USGS1997

Equilibrium responses of global net primary production and carbon storage to doubled atmospheric carbon dioxide: Sensitivity to changes in vegetation nitrogen concentration

We ran the terrestrial ecosystem model (TEM) for the globe at 0.5° resolution for atmospheric CO 2 concentrations of 340 and 680 parts per million by volume (ppmv) to evaluate global and regional responses of net primary production (NPP) and carbon storage to elevated CO 2 for their sensitivity to changes in vegetation nitrogen concentration. At 340 ppmv, TEM estimated global NPP of 49.0 10 15 g (Pg) C yr −1 and global total carbon storage of 1701.8 Pg C; the estimate of total carbon storage does not include the carbon content of inert soil organic matter. For the reference simulation in which doubled atmospheric CO 2 was accompanied with no change in vegetation nitrogen concentration, global NPP increased 4.1 Pg C yr −1 (8.3%), and global total carbon storage increased 114.2 Pg C. To examine sensitivity in the global responses of NPP and carbon storage to decreases in the nitrogen concentration of vegetation, we compared doubled CO 2 responses of the reference TEM to simulations in which the vegetation nitrogen concentration was reduced without influencing decomposition dynamics (“lower N” simulations) and to simulations in which reductions in vegetation nitrogen concentration influence decomposition dynamics (“lower N+D” simulations). We conducted three lower N simulations and three lower N+D simulations in which we reduced the nitrogen concentration of vegetation by 7.5, 15.0, and 22.5%. In the lower N simulations, the response of global NPP to doubled atmospheric CO 2 increased approximately 2 Pg C yr −1 for each incremental 7.5% reduction in vegetation nitrogen concentration, and vegetation carbon increased approximately an additional 40 Pg C, and soil carbon increased an additional 30 Pg C, for a total carbon storage increase of approximately 70 Pg C. In the lower N+D simulations, the responses of NPP and vegetation carbon storage were relatively insensitive to differences in the reduction of nitrogen concentration, but soil carbon storage showed a large change. The insensitivity of NPP in the N+D simulations occurred because potential enhancements in NPP associated with reduced vegetation nitrogen concentration were approximately offset by lower nitrogen availability associated with the decomposition dynamics of reduced litter nitrogen concentration. For each 7.5% reduction in vegetation nitrogen concentration, soil carbon increased approximately an additional 60 Pg C, while vegetation carbon storage increased by only approximately 5 Pg C. As the reduction in vegetation nitrogen concentration gets greater in the lower N+D simulations, more of the additional carbon storage tends to become concentrated in the north temperate-boreal region in comparison to the tropics. Other studies with TEM show that elevated CO 2 more than offsets the effects of climate change to cause increased carbon storage. The results of this study indicate that carbon storage would be enhanced by the influence of changes in plant nitrogen concentration on carbon assimilation and decomposition rates. Thus changes in vegetation nitrogen concentration may have important implications for the ability of the terrestrial biosphere to mitigate increases in the atmospheric concentration of CO 2 and climate changes associated with the increases.

Global Biogeochemical Cycles↗