In order to protect estuarine resources, managers must be able to discern the effects of natural conditions and non-point source effects, and separate them from multiple anthropogenic point source effects. Our approach was to evaluate benthic community assemblages, riverine nitro...
WHAT TO DO IF THERE IS NO REFERENCE SYSTEM
Efficient management and regulation of anthropogenic point source inputs requires a demonstrated and measurable ecological effect. In all ecosystems, the evaluation of anthropogenic effects is confounded by the effects of naturally existing environmental factors and river nonpoin...
Wilkison, D.H.; Armstrong, D.J.; Hampton, S.A.
2009-01-01
From 1998 through 2007, over 750 surface-water or bed-sediment samples in the Blue River Basin - a largely urban basin in metropolitan Kansas City - were analyzed for more than 100 anthropogenic compounds. Compounds analyzed included nutrients, fecal-indicator bacteria, suspended sediment, pharmaceuticals and personal care products. Non-point source runoff, hydrologic alterations, and numerous waste-water discharge points resulted in the routine detection of complex mixtures of anthropogenic compounds in samples from basin stream sites. Temporal and spatial variations in concentrations and loads of nutrients, pharmaceuticals, and organic wastewater compounds were observed, primarily related to a site's proximity to point-source discharges and stream-flow dynamics. ?? 2009 ASCE.
NASA Astrophysics Data System (ADS)
Steenhuisen, Frits; Wilson, Simon J.
2015-07-01
Mercury is a global pollutant that poses threats to ecosystem and human health. Due to its global transport, mercury contamination is found in regions of the Earth that are remote from major emissions areas, including the Polar regions. Global anthropogenic emission inventories identify important sectors and industries responsible for emissions at a national level; however, to be useful for air transport modelling, more precise information on the locations of emission is required. This paper describes the methodology applied, and the results of work that was conducted to assign anthropogenic mercury emissions to point sources as part of geospatial mapping of the 2010 global anthropogenic mercury emissions inventory prepared by AMAP/UNEP. Major point-source emission sectors addressed in this work account for about 850 tonnes of the emissions included in the 2010 inventory. This work allocated more than 90% of these emissions to some 4600 identified point source locations, including significantly more point source locations in Africa, Asia, Australia and South America than had been identified during previous work to geospatially-distribute the 2005 global inventory. The results demonstrate the utility and the limitations of using existing, mainly public domain resources to accomplish this work. Assumptions necessary to make use of selected online resources are discussed, as are artefacts that can arise when these assumptions are applied to assign (national-sector) emissions estimates to point sources in various countries and regions. Notwithstanding the limitations of the available information, the value of this procedure over alternative methods commonly used to geo-spatially distribute emissions, such as use of 'proxy' datasets to represent emissions patterns, is illustrated. Improvements in information that would facilitate greater use of these methods in future work to assign emissions to point-sources are discussed. These include improvements to both national (geo-referenced) emission inventories and also to other resources that can be employed when such national inventories are lacking.
Establishing an Anthropogenic Nitrogen Baseline Using Native American Shell Middens
Narragansett Bay, Rhode Island, has been heavily influenced by anthropogenic nutrients for more than 200 years. Recent efforts to improve water quality have cut sewage nitrogen (N) loads to this point source estuary by more than half. Given that the bay has been heavily fertilize...
Anthropogenic impervious surfaces are leading contributors to non-point-source water pollution in urban watersheds. These human-created surfaces include such features as roads, parking lots, rooftops, sideways, and driveways. Aerial photography provides a historical vehicle for...
Heavy metals in marine coastal sediments: assessing sources, fluxes, history and trends.
Frignani, Mauro; Bellucci, Luca Giorgio
2004-01-01
Examples are presented from the Adriatic Sea, the Ligurian Sea and the Venice Lagoon to illustrate different approaches to the study of anthropogenic metals in marine coastal sediments. These examples refer to studies of areal distribution and transport mechanisms, individuation of the sources, sediment dating, chronology of the fluxes, present and past trends. In particular, some of the findings achieved in studying the Venice Lagoon are discussed from the point of view of anthropogenic changes both in sediment composition and contaminant fluxes.
Merschel, Gila; Bau, Michael
2015-11-15
High-technology metals - such as the rare earth elements (REE) - have become emerging contaminants in the hydrosphere, yet little is known about their bioavailability. The Rhine River and the Weser River in Germany are two prime examples of rivers that are subjected to anthropogenic REE input. While both rivers carry significant loads of anthropogenic Gd, originating from contrast agents used for magnetic resonance imaging, the Rhine River also carries large amounts of anthropogenic La and lately Sm which are discharged into the river from an industrial point source. Here, we assess the bioavailability of these anthropogenic microcontaminants in these rivers by analyzing the aragonitic shells of the freshwater bivalve Corbicula fluminea. Concentrations of purely geogenic REE in shells of comparable size cover a wide range of about one order of magnitude between different sampling sites. At a given sampling site, geogenic REE concentrations depend on shell size, i.e. mussel age. Although both rivers show large positive Gd anomalies in their dissolved loads, no anomalous enrichment of Gd relative to the geogenic REE can be observed in any of the analyzed shells. This indicates that the speciations of geogenic and anthropogenic Gd in the river water differ from each other and that the geogenic, but not the anthropogenic Gd is incorporated into the shells. In contrast, all shells sampled at sites downstream of the industrial point source of anthropogenic La and Sm in the Rhine River show positive La and Sm anomalies, revealing that these anthropogenic REE are bioavailable. Only little is known about the effects of long-term exposure to dissolved REE and their general ecotoxicity, but considering that anthropogenic Gd and even La have already been identified in German tap water and that anthropogenic La and Sm are bioavailable, this should be monitored and investigated further. Copyright © 2015 Elsevier B.V. All rights reserved.
Mercury Contaminated Sediment Sites: A Review Of Remedial Solutions
Mercury (Hg) can accumulate in sediment from point and non-point sources, depending on a number of physical, chemical, biological, geological and anthropogenic environmental processes. It is believed that the associated Hg contamination in aquatic systems can be decreased by imp...
NASA Astrophysics Data System (ADS)
Liu, F.; Joiner, J.; Choi, S.; Krotkov, N. A.; Li, C.; Fioletov, V. E.; McLinden, C. A.
2017-12-01
Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor have been used to detect emissions from large point sources using an innovative estimation technique. Emissions from about 500 sources have been quantified individually based on OMI observations, accounting for about a half of total reported anthropogenic SO2 emissions. We developed a new emission inventory, OMI-HTAP, by combining these OMI-based emission estimates and the conventional bottom-up inventory. OMI-HTAP includes OMI-based estimates for over 400 point sources and is gap-filled with the emission grid map of the latest available global bottom-up emission inventory (HTAP v2.2) for the rest of sources. We have evaluated the OMI-HTAP inventory by performing simulations with the Goddard Earth Observing System version 5 (GEOS-5) model. The GEOS-5 simulated SO2 concentrations driven by both the HTAP and the OMI-HTAP inventory were compared against in-situ and satellite measurements. Results show that the OMI-HTAP inventory improves the model agreement with observations, in particular over the US, India and the Middle East. Additionally, simulations with the OMI-HTAP inventory capture the major trends of anthropogenic SO2 emissions over the world and highlight the influence of missing sources in the bottom-up inventory.
Zereini, F; Dirksen, F; Skerstupp, B; Urban, H
1998-01-01
Soil samples from the area of Hanau (Hessen, Germany) were analyzed for anthropogenic platinum-group elements (PGE). The results confirm the existence of two different sources for anthropogenic PGE: 1. automotive catalysts, and 2. PGE-processing plants. Both sources emit qualitatively and quantitatively different PGE spectra and PGE interelemental ratios (especially the Pt/Rh ratio). Elevated PGE values which are due to automotive catalysts are restricted to a narrow-range along roadside soil, whereas those due to PGE-processing plants display a large-area dispersion. The emitted PGE-containing particles in the case of automotive catalysts are subject to transport by wind and water, whereas those from PGE-processing plants are preferably transported by wind. This points to a different aerodynamic particle size. Pt, Pd, and Rh concentrations along motorways are dependent on the amount of traffic and the driving characteristics.
Guo, Xueru; Zuo, Rui; Meng, Li; Wang, Jinsheng; Teng, Yanguo; Liu, Xin; Chen, Minhua
2018-01-01
Globally, groundwater resources are being deteriorated by rapid social development. Thus, there is an urgent need to assess the combined impacts of natural and enhanced anthropogenic sources on groundwater chemistry. The aim of this study was to identify seasonal characteristics and spatial variations in anthropogenic and natural effects, to improve the understanding of major hydrogeochemical processes based on source apportionment. 34 groundwater points located in a riverside groundwater resource area in northeast China were sampled during the wet and dry seasons in 2015. Using principal component analysis and factor analysis, 4 principal components (PCs) were extracted from 16 groundwater parameters. Three of the PCs were water-rock interaction (PC1), geogenic Fe and Mn (PC2), and agricultural pollution (PC3). A remarkable difference (PC4) was organic pollution originating from negative anthropogenic effects during the wet season, and geogenic F enrichment during the dry season. Groundwater exploitation resulted in dramatic depression cone with higher hydraulic gradient around the water source area. It not only intensified dissolution of calcite, dolomite, gypsum, Fe, Mn and fluorine minerals, but also induced more surface water recharge for the water source area. The spatial distribution of the PCs also suggested the center of the study area was extremely vulnerable to contamination by Fe, Mn, COD, and F−. PMID:29415516
Strategies for satellite-based monitoring of CO2 from distributed area and point sources
NASA Astrophysics Data System (ADS)
Schwandner, Florian M.; Miller, Charles E.; Duren, Riley M.; Natraj, Vijay; Eldering, Annmarie; Gunson, Michael R.; Crisp, David
2014-05-01
Atmospheric CO2 budgets are controlled by the strengths, as well as the spatial and temporal variabilities of CO2 sources and sinks. Natural CO2 sources and sinks are dominated by the vast areas of the oceans and the terrestrial biosphere. In contrast, anthropogenic and geogenic CO2 sources are dominated by distributed area and point sources, which may constitute as much as 70% of anthropogenic (e.g., Duren & Miller, 2012), and over 80% of geogenic emissions (Burton et al., 2013). Comprehensive assessments of CO2 budgets necessitate robust and highly accurate satellite remote sensing strategies that address the competing and often conflicting requirements for sampling over disparate space and time scales. Spatial variability: The spatial distribution of anthropogenic sources is dominated by patterns of production, storage, transport and use. In contrast, geogenic variability is almost entirely controlled by endogenic geological processes, except where surface gas permeability is modulated by soil moisture. Satellite remote sensing solutions will thus have to vary greatly in spatial coverage and resolution to address distributed area sources and point sources alike. Temporal variability: While biogenic sources are dominated by diurnal and seasonal patterns, anthropogenic sources fluctuate over a greater variety of time scales from diurnal, weekly and seasonal cycles, driven by both economic and climatic factors. Geogenic sources typically vary in time scales of days to months (geogenic sources sensu stricto are not fossil fuels but volcanoes, hydrothermal and metamorphic sources). Current ground-based monitoring networks for anthropogenic and geogenic sources record data on minute- to weekly temporal scales. Satellite remote sensing solutions would have to capture temporal variability through revisit frequency or point-and-stare strategies. Space-based remote sensing offers the potential of global coverage by a single sensor. However, no single combination of orbit and sensor provides the full range of temporal sampling needed to characterize distributed area and point source emissions. For instance, point source emission patterns will vary with source strength, wind speed and direction. Because wind speed, direction and other environmental factors change rapidly, short term variabilities should be sampled. For detailed target selection and pointing verification, important lessons have already been learned and strategies devised during JAXA's GOSAT mission (Schwandner et al, 2013). The fact that competing spatial and temporal requirements drive satellite remote sensing sampling strategies dictates a systematic, multi-factor consideration of potential solutions. Factors to consider include vista, revisit frequency, integration times, spatial resolution, and spatial coverage. No single satellite-based remote sensing solution can address this problem for all scales. It is therefore of paramount importance for the international community to develop and maintain a constellation of atmospheric CO2 monitoring satellites that complement each other in their temporal and spatial observation capabilities: Polar sun-synchronous orbits (fixed local solar time, no diurnal information) with agile pointing allow global sampling of known distributed area and point sources like megacities, power plants and volcanoes with daily to weekly temporal revisits and moderate to high spatial resolution. Extensive targeting of distributed area and point sources comes at the expense of reduced mapping or spatial coverage, and the important contextual information that comes with large-scale contiguous spatial sampling. Polar sun-synchronous orbits with push-broom swath-mapping but limited pointing agility may allow mapping of individual source plumes and their spatial variability, but will depend on fortuitous environmental conditions during the observing period. These solutions typically have longer times between revisits, limiting their ability to resolve temporal variations. Geostationary and non-sun-synchronous low-Earth-orbits (precessing local solar time, diurnal information possible) with agile pointing have the potential to provide, comprehensive mapping of distributed area sources such as megacities with longer stare times and multiple revisits per day, at the expense of global access and spatial coverage. An ad hoc CO2 remote sensing constellation is emerging. NASA's OCO-2 satellite (launch July 2014) joins JAXA's GOSAT satellite in orbit. These will be followed by GOSAT-2 and NASA's OCO-3 on the International Space Station as early as 2017. Additional polar orbiting satellites (e.g., CarbonSat, under consideration at ESA) and geostationary platforms may also become available. However, the individual assets have been designed with independent science goals and requirements, and limited consideration of coordinated observing strategies. Every effort must be made to maximize the science return from this constellation. We discuss the opportunities to exploit the complementary spatial and temporal coverage provided by these assets as well as the crucial gaps in the capabilities of this constellation. References Burton, M.R., Sawyer, G.M., and Granieri, D. (2013). Deep carbon emissions from volcanoes. Rev. Mineral. Geochem. 75: 323-354. Duren, R.M., Miller, C.E. (2012). Measuring the carbon emissions of megacities. Nature Climate Change 2, 560-562. Schwandner, F.M., Oda, T., Duren, R., Carn, S.A., Maksyutov, S., Crisp, D., Miller, C.E. (2013). Scientific Opportunities from Target-Mode Capabilities of GOSAT-2. NASA Jet Propulsion Laboratory, California Institute of Technology, Pasadena CA, White Paper, 6p., March 2013.
Corbitt, Elizabeth S.; Jacob, Daniel J.; Holmes, Christopher D.; Streets, David G.; Sunderland, Elsie M.
2011-01-01
Global policies regulating anthropogenic mercury require an understanding of the relationship between emitted and deposited mercury on intercontinental scales. Here we examine source-receptor relationships for present-day conditions and for four 2050 IPCC scenarios encompassing a range of economic development and environmental regulation projections. We use the GEOS-Chem global model to track mercury from its point of emission through rapid cycling in surface ocean and land reservoirs to its accumulation in longer-lived ocean and soil pools. Deposited mercury has a local component (emitted HgII, lifetime of 3.7 days against deposition) and a global component (emitted Hg0, lifetime of 6 months against deposition). Fast recycling of deposited mercury through photoreduction of HgII and re-emission of Hg0 from surface reservoirs (ice, land, surface ocean) increases the effective lifetime of anthropogenic mercury to 9 months against loss to legacy reservoirs (soil pools and the subsurface ocean). This lifetime is still sufficiently short that source-receptor relationships have a strong hemispheric signature. Asian emissions are the largest source of anthropogenic deposition to all ocean basins, though there is also regional source influence from upwind continents. Current anthropogenic emissions account for only about one-third of mercury deposition to the global ocean with the remainder from natural and legacy sources. However, controls on anthropogenic emissions would have the added benefit of reducing the legacy mercury re-emitted to the atmosphere. Better understanding is needed of the timescales for transfer of mercury from active pools to stable geochemical reservoirs. PMID:22050654
NASA Astrophysics Data System (ADS)
Voss, Anja; Bärlund, Ilona; Punzet, Manuel; Williams, Richard; Teichert, Ellen; Malve, Olli; Voß, Frank
2010-05-01
Although catchment scale modelling of water and solute transport and transformations is a widely used technique to study pollution pathways and effects of natural changes, policies and mitigation measures there are only a few examples of global water quality modelling. This work will provide a description of the new continental-scale model of water quality WorldQual and the analysis of model simulations under changed climate and anthropogenic conditions with respect to changes in diffuse and point loading as well as surface water quality. BOD is used as an indicator of the level of organic pollution and its oxygen-depleting potential, and for the overall health of aquatic ecosystems. The first application of this new water quality model is to river systems of Europe. The model itself is being developed as part of the EU-funded SCENES Project which has the principal goal of developing new scenarios of the future of freshwater resources in Europe. The aim of the model is to determine chemical fluxes in different pathways combining analysis of water quantity with water quality. Simple equations, consistent with the availability of data on the continental scale, are used to simulate the response of in-stream BOD concentrations to diffuse and anthropogenic point loadings as well as flow dilution. Point sources are divided into manufacturing, domestic and urban loadings, whereas diffuse loadings come from scattered settlements, agricultural input (for instance livestock farming), and also from natural background sources. The model is tested against measured longitudinal gradients and time series data at specific river locations with different loading characteristics like the Thames that is driven by domestic loading and Ebro with relative high share of diffuse loading. With scenario studies the influence of climate and anthropogenic changes on European water resources shall be investigated with the following questions: 1. What percentage of river systems will have degraded water quality due to different driving forces? 2. How will climate change and changes in wastewater discharges affect water quality? For the analysis these scenario aspects are included: 1. climate with changed runoff (affecting diffuse pollution and loading from sealed areas), river discharge (causing dilution or concentration of point source pollution) and water temperature (affecting BOD degradation). 2. Point sources with changed population (affecting domestic pollution), connectivity to treatment plants (influencing domestic and manufacturing pollution as well as input from sealed areas and scattered settlements).
NASA Astrophysics Data System (ADS)
Irfan, M. I.; Meisel, T.
2012-04-01
Concentration of nickel and chromium in any part of the ecosystem is important for environmental concerns in particular human health due to the reason that some species of them can cause health problem e.g. dermatitis and cancer. Sediment samples collected form a river Vordernberger Bach (Leoben, Austria) in an alpine region and soil samples collected in an area adjacent to steel production unit in same narrow valley were investigated. In previous studies a correlation between magnetic susceptibility values and concentration of nickel and chromium showed that a magnetic susceptibility meter can be used to point out the contaminated areas as in-situ device. The purpose of the whole study is to understand the real (point or diffuse, anthropogenic or geogenic) sources of contamination of soils, water and river sediments through heavy metal deposition. Unseparated, magnetic and non-magnetic fractions of soil samples were investigated for geochemical and mineralogical aspects with XRF, ICP-MS, EMPA, Multi-Functional Kappabridge (MFK1) and laser ablation coupled with ICP-MS. Mineralogical study of sediment samples for several sampling points with higher Ni and Cr content was performed. Sediment samples were sieved below 1.4 mm and then a concentrate of heavy minerals was prepared in the field through panning. Concentrated heavy minerals were then subjected for heavy liquid separation in the laboratory. Separated magnetic and non-magnetic fractions below 0.71/0.1 mm and density greater than 2.9 g/cm3 were selected for mineralogical investigation. The abundance of typical anthropogenic particles, e.g., spherical, tinder, roasted ores, iron and steel mill slag was observed under the microscope. Magnetite (mostly anthropogenic), maghemite, chromspinel, chromite (type I & II), (Ca,Al)-ferrite, wustite, apatite (anthropogenic), olivine mixed crystals, calcium silicate and spinel (anthropogenic) are found in magnetic fraction. Non-magnetic fractions contain hematite, siderite, ankerite, corundum (anthropogenic), garnet, chlorite, titanium oxide minerals (ilmenite, rutile, titanite) and amphibole etc. The observed significant increase in heavy metal content from the source region of the Vordernberger Bach at 1500 m above sea level to the confluence of the Vordernberger Bach with the Mur River at 540 m AMSL can be attributed to anthropogenic influence. As expected, the anthropogenic input is more pronounced in the vicinity of historic and current iron and steel production.
Status of metal levels and their potential sources of contamination in Southeast Asian rivers.
Chanpiwat, Penradee; Sthiannopkao, Suthipong
2014-01-01
To assess the concentration and status of metal contaminants in four major Southeast Asian river systems, water were collected from the Tonle Sap-Bassac Rivers (Cambodia), Citarum River (Indonesia), lower Chao Phraya River (Thailand), and Saigon River (Vietnam) in both dry and wet seasons. The target elements were Be, Al, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn, As, Se, Mo, Ag, Cd, Ba, Tl, and Pb and the concentrations exceeded the background metal concentrations by 1- to 88-fold. This distinctly indicates enrichment by human urban area activities. The results of a normalization technique used to distinguish natural from enriched metal concentrations confirmed contamination by Al, Cd, Co, Mn, Ni, Pb, and Zn. Cluster analysis revealed the probable source of metals contamination in most sampling sites on all rivers studied to be anthropogenic, including industrial, commercial, and residential activities. Stable lead isotopes analyses applied to track the sources and pathways of anthropogenic lead furthermore confirmed that anthropogenic sources of metal contaminated these rivers. Discharges of wastewater from both industrial and household activities were major contributors of Pb into the rivers. Non-point sources, especially road runoff and street dust, also contributed contamination from Pb and other metals.
Effects of anthropogenic developments on common raven nesting biology in the West Mojave Desert.
Kristan, William B; Boarman, William I
2007-09-01
Subsidized predators may affect prey abundance, distribution, and demography. Common Ravens (Corvus corax) are anthropogenically subsidized throughout their range and, in the Mojave Desert, have increased in number dramatically over the last 3-4 decades. Human-provided food resources are thought to be important drivers of raven population growth, but human developments add other features as well, such as nesting platforms. From 1996 to 2000, we examined the nesting ecology of ravens in the Mojave Desert, relative to anthropogenic developrhent. Ravens nested disproportionately near point sources of food and water subsidies (such as towns, landfills, and ponds) but not near roads (sources of road-killed carrion), even though both sources of subsidy enhanced fledging success. Initiation of breeding activity was more likely when a nest from the previous year was present at the start of a breeding season but was not affected by access to food. The relative effect of environmental modifications on fledging success varied from year to year, but the effect of access to human-provided resources was comparatively consistent, suggesting that humans provide consistently high-quality breeding habitat for ravens. Anthropogenic land cover types in the desert are expected to promote raven population growth and to allow ravens to occupy parts of the desert that otherwise would not support them. Predatory impacts of ravens in the Mojave Desert can therefore be considered indirect effects of anthropogenic development.
Miler, Miloš; Gosar, Mateja
2013-12-01
Solid particles in snow deposits, sampled in mining and Pb-processing area of Žerjav, Slovenia, have been investigated using scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDS). Identified particles were classified as geogenic-anthropogenic, anthropogenic, and secondary weathering products. Geogenic-anthropogenic particles were represented by scarce Zn- and Pb-bearing ore minerals, originating from mine waste deposit. The most important anthropogenic metal-bearing particles in snow were Pb-, Sb- and Sn-bearing oxides and sulphides. The morphology of these particles showed that they formed at temperatures above their melting points. They were most abundant in snow sampled closest to the Pb-processing plant and least abundant in snow taken farthest from the plant, thus indicating that Pb processing was their predominant source between the last snowfall and the time of sampling. SEM/EDS analysis showed that Sb and Sn contents in these anthropogenic phases were higher and more variable than in natural Pb-bearing ore minerals. The most important secondary weathering products were Pb- and Zn-containing Fe-oxy-hydroxides whose elemental composition and morphology indicated that they mostly resulted from oxidation of metal-bearing sulphides emitted from the Pb-processing plant. This study demonstrated the importance of single particle analysis using SEM/EDS for differentiation between various sources of metals in the environment.
IMPERVIOUS SURFACE RESEARCH IN THE MID-ATLANTIC
Anthropogenic impervious surfaces have an important relationship with non-point source pollution (NPS) in urban watersheds. These human-created surfaces include such features as roads, parking lots, rooftops, sidewalks, and driveways. The amount of impervious surface area in a ...
Volatile halogenated hydrocarbons over the western Pacific between 43° and 4°N
NASA Astrophysics Data System (ADS)
Quack, Birgit; Suess, Erwin
1999-01-01
A spectrum of halogenated hydrocarbon compounds in marine air masses were surveyed over an area in the western Pacific between 43°N, 150°E and 4°N, 113°E in September 1994. The ship's track between northern Japan and Singapore traversed three climatic zones of the northern hemisphere. Recently polluted air, clean marine air derived from the central Pacific Ocean from different latitudes, and marine air from the Indonesian archipelago were collected. Tetrachloroethene and trichloroethene of anthropogenic origin, brominated halocarbons as tribromomethane, dibromochloromethane and bromodichloromethane of anthropogenic and natural sources, and other trace gases were measured in the air samples. Very sparse data on the distribution of these compounds exist for the western Pacific atmosphere. The distribution patterns of the compounds were related to synoptic-scale meteorology, spatial conditions, and origin of the air masses. Anthropogenic and natural sources for both chlorinated and brominated substances were identified. Tetrachloroethene and trichloroethene concentrations and their ratios identify anthropogenic sources. Their mixing ratios were quite low compared to previously published data. They are in agreement with expected low concentrations of photochemically active substances during autumn, with an overall decrease in concentrations toward lower latitudes, and with a decrease of emissions during recent years. Strong evidence for a natural source of trichloroethene was discovered in the tropical region. The concentrations of naturally released brominated species were high compared to other measurements over the Pacific. Gradients toward the coasts and elevated concentrations in air masses influenced by coastal emissions point to significant coastal sources of these compounds. The trace gas composition of anthropogenic and natural compounds clearly identified the air masses which were traversed during the cruise.
USEPA EPIC IMPERVIOUS SURFACE RESEARCH IN THE MID-ATLANTIC
Anthropogenic impervious surfaces have an important relationship with non-point source pollution (NPS) in urban watersheds. These human-created surfaces include such features as roads, parking lots, rooftops, sidewalks, and driveways. The amount of impervious surface area in a ...
Lessons Learned from OMI Observations of Point Source SO2 Pollution
NASA Technical Reports Server (NTRS)
Krotkov, N.; Fioletov, V.; McLinden, Chris
2011-01-01
The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. Although anthropogenic SO2 signals may not be detectable in a single OMI pixel, it is possible to see the source and determine its exact location by averaging a large number of individual measurements. We describe new techniques for spatial and temporal averaging that have been applied to the OMI SO2 data to determine the spatial distributions or "fingerprints" of SO2 burdens from top 100 pollution sources in North America. The technique requires averaging of several years of OMI daily measurements to observe SO2 pollution from typical anthropogenic sources. We found that the largest point sources of SO2 in the U.S. produce elevated SO2 values over a relatively small area - within 20-30 km radius. Therefore, one needs higher than OMI spatial resolution to monitor typical SO2 sources. TROPOMI instrument on the ESA Sentinel 5 precursor mission will have improved ground resolution (approximately 7 km at nadir), but is limited to once a day measurement. A pointable geostationary UVB spectrometer with variable spatial resolution and flexible sampling frequency could potentially achieve the goal of daily monitoring of SO2 point sources and resolve downwind plumes. This concept of taking the measurements at high frequency to enhance weak signals needs to be demonstrated with a GEOCAPE precursor mission before 2020, which will help formulating GEOCAPE measurement requirements.
STREAM CORRIDOR RESTORATION AND ITS POTENTIAL TO IMPROVE WATER QUALITY
Watershed stream corridors are being degraded by anthropogenic impacts of increased flow from runoff, sediment loading from erosion and contaminants such as nitrate from non-point sources. One solution is to restore stream corridors with bank stabilization and energy dissipation ...
Multi-scale trends analysis of landscape stressors in an urbanizing coastal watershed
Anthropogenic land based stressors within a watershed can deliver major impacts to downstream and adjacent coastal waterways affecting water quality and estuarine habitats. Our research focused on a subset of non-point sources of watershed stressors specifically, human population...
Effects of anthropogenic developments on common Raven nesting biology in the west Mojave Desert
Kristan, W. B.; Boarman, W.I.
2007-01-01
Subsidized predators may affect prey abundance, distribution, and demography. Common Ravens (Corvus corax) are anthropogenically subsidized throughout their range and, in the Mojave Desert, have increased in number dramatically over the last 3-4 decades. Human-provided food resources are thought to be important drivers of raven population growth, but human developments add other features as well, such as nesting platforms. From 1996 to 2000, we examined the nesting ecology of ravens in the Mojave Desert, relative to anthropogenic development. Ravens nested disproportionately near point sources of food and water subsidies (such as towns, landfills, and ponds) but not near roads (sources of road-killed carrion), even though both sources of subsidy enhanced fledging success. Initiation of breeding activity was more likely when a nest from the previous year was present at the start of a breeding season but was not affected by access to food. The relative effect of environmental modifications on fledging success varied from year to year, but the effect of access to humanprovided resources was comparatively consistent, suggesting that humans provide consistently high-quality breeding habitat for ravens. Anthropogenic land cover types in the desert are expected to promote raven population growth and to allow ravens to occupy parts of the desert that otherwise would not support them. Predatory impacts of ravens in the Mojave Desert can therefore be considered indirect effects of anthropogenic development. ?? 2007 by the Ecological Society of America.
Lead concentration and isotope chronology in two coastal environments in Western and South East Asia
NASA Astrophysics Data System (ADS)
Carrasco, G. G.; Chen, M.; Boyle, E. A.; Zhao, N.; Nurhati, I. S.; Gevao, B.; al Ghadban, A.; Switzer, A.; Lee, J. M.
2014-12-01
Lead is a trace metal that is closely related to anthropogenic activity, mainly via leaded gasoline and coal combustion. The study of lead concentrations and isotopes in seawater, sediments, corals and aerosols allows for a systematic look at its sources and their time evolution in a natural environment. We will discuss results from two projects in Western and South East Asia, regions that have seen dramatic socio-economical changes over the past half-century that may have left environmental signals. These results highlight the usefulness of the method, indicate the degree of complexity of these systems, and point to the need for a continuous monitoring of anthropogenic trace metals in the small-medium coastal scale to be able to asses the larger scale effects of human activity. On the one hand, coastal Kuwait is heavily influenced by the Shat al-Arab river and shows a clear anthropogenic signature from Kuwait city. A mix of two sources can be tracked through the coral and sediment chronological records, with Pb206/Pb207 ratios (1.202 and 1.151) that approach the suspected source values (1.21 and 1.12) and eliminate the possibility of other sources. Through a wide sediment geographic distribution, the strength of the anthropogenic signature is modulated. On the other hand, Singapore offers a more complex system, where an apparent mix of two sources (extreme isotope ratios 1.215 and ~1.14) occurs also, but where either an unresolved potentially important third source (isotope ratio ~1.18), or an isotope exchange process should be invoked. The sediment and coral records allows us to track the changes through time; however, there seems to be incongruence with the aerosol isotope record. Further potential sources are being explored currently and will be discussed.
WATERSHEED NUTRIENT INPUTS, PHYTOPLANKTON ACCUMULATION, AND C STOCKS IN CHESAPEAKE BAY
Inputs of N and P to Chesapeake Bay have been enhanced by anthropogenic activities. Fertilizers, developed areas, N emissions, and industrial effluents contribute to point and diffuse sources currently 2-20X higher than those from undisturbed watersheds. Enhanced nutrient inputs ...
Wang, Yujue; Liu, Dongyan; Dong, Zhijun; Di, Baoping; Shen, Xuhong
2012-12-01
The temporal and spatial distributions of dissolved inorganic nitrogen (DIN), dissolved organic nitrogen (DON), soluble reactive phosphorus (SRP) and dissolved reactive silica (DRSi) together with chlorophyll-a, temperature and salinity were analyzed monthly from December 2008 to March 2010 at four zones in Sishili Bay located in the northern Yellow Sea. The nutrient distribution was impacted by seasonal factors (biotic factors, temperature and wet deposition), physical factors (water exchange) and anthropogenic loadings. The seasonal variations of nutrients were mainly determined by the seasonal factors and the spatial distribution of nutrients was mainly related to water exchange. Anthropogenic loadings for DIN, SRP and DRSi were mainly from point sources, but for DON, non-point sources were also important. Nutrient limitation has changed from DIN in 1997 to SRP and DRSi in 2010, and this has resulted in changes in the dominant red tide species from diatom to dinoflagellates. Copyright © 2012 Elsevier Ltd. All rights reserved.
Fernández-Camacho, R; de la Rosa, J D; Sánchez de la Campa, A M
2016-05-15
This study presents a 17-years air quality database comprised of different parameters corresponding to the largest city in the south of Spain (Seville) where atmospheric pollution is frequently attributed to traffic emissions and is directly affected by Saharan dust outbreaks. We identify the PM10 contributions from both natural and anthropogenic sources in this area associated to different air mass origins. Hourly, daily and seasonal variation of PM10 and gaseous pollutant concentrations (CO, NO2 and SO2), all of them showing negative trends during the study period, point to the traffic as one of the main sources of air pollution in Seville. Mineral dust, secondary inorganic compounds (SIC) and trace elements showed higher concentrations under North African (NAF) air mass origins than under Atlantic. We observe a decreasing trend in all chemical components of PM10 under both types of air masses, NAF and Atlantic. Principal component analysis using more frequent air masses in the area allows the identification of five PM10 sources: crustal, regional, marine, traffic and industrial. Natural sources play a more relevant role during NAF events (20.6 μg · m(-3)) than in Atlantic episodes (13.8 μg · m(-3)). The contribution of the anthropogenic sources under NAF doubles the one under Atlantic conditions (33.6 μg · m(-3) and 15.8 μg · m(-3), respectively). During Saharan dust outbreaks the frequent accumulation of local anthropogenic pollutants in the lower atmosphere results in poor air quality and an increased risk of mortality. The results are relevant when analysing the impact of anthropogenic emissions on the exposed population in large cities. The increase in potentially toxic elements during Saharan dust outbreaks should also be taken into account when discounting the number of exceedances attributable to non-anthropogenic or natural origins. Copyright © 2016 Elsevier B.V. All rights reserved.
Occurrence of THM and NDMA precursors in a watershed: Effect of seasons and anthropogenic pollution.
Aydin, Egemen; Yaman, Fatma Busra; Ates Genceli, Esra; Topuz, Emel; Erdim, Esra; Gurel, Melike; Ipek, Murat; Pehlivanoglu-Mantas, Elif
2012-06-30
In pristine watersheds, natural organic matter is the main source of disinfection by-product (DBP) precursors. However, the presence of point or non-point pollution sources in watersheds may lead to increased levels of DBP precursors which in turn form DBPs in the drinking water treatment plant upon chlorination or chloramination. In this study, water samples were collected from a lake used to obtain drinking water for Istanbul as well as its tributaries to investigate the presence of the precursors of two disinfection by-products, trihalomethanes (THM) and N-nitrosodimethylamine (NDMA). In addition, the effect of seasons and the possible relationships between these precursors and water quality parameters were evaluated. The concentrations of THM and NDMA precursors measured as total THM formation potential (TTHMFP) and NDMA formation potential (NDMAFP) ranged between 126 and 1523μg/L THM and <2 and 1648ng/L NDMA, respectively. Such wide ranges imply that some of the tributaries are affected by anthropogenic pollution sources, which is also supported by high DOC, Cl(-) and NH(3) concentrations. No significant correlation was found between the water quality parameters and DBP formation potential, except for a weak correlation between NDMAFP and DOC concentrations. The effect of the sampling location was more pronounced than the seasonal variation due to anthropogenic pollution in some tributaries and no significant correlation was obtained between the seasons and water quality parameters. Copyright © 2012 Elsevier B.V. All rights reserved.
Estimating Anthropogenic Emissions of Hydrogen Chloride and Fine Particulate Chloride in China
NASA Astrophysics Data System (ADS)
Fu, X.; Wang, T.; Wang, S.; Zhang, L.
2017-12-01
Nitryl chloride (ClNO2) can significantly impact the atmospheric photochemistry via photolysis and subsequent reactions of chlorine radical with other gases. The formation of ClNO2 in the atmosphere is sensitive to the emissions of chlorine-containing particulates from oceanic and anthropogenic sources. For China, the only available anthropogenic chlorine emission inventory was compiled for the year 1990 with a coarse resolution of 1 degree. In this study, we developed an up-to-date anthropogenic inventory of hydrogen chloride (HCl) and fine particulate chloride (Cl-) emissions in China for the year 2014, including coal burning, industrial processes, biomass burning and waste burning. Bottom-up and top-down methodologies were combined. Detailed local data (e.g. Cl content in coal, control technologies, etc.) were collected and applied. In order to improve the spatial resolution of emissions, detailed point source information were collected for coal-fired power plants, cement factories, iron & steel factories and waste incineration factories. Uncertainties of this emission inventory and their major causes were analyzed using the Monte Carlo method. This work enables better quantification of the ClNO2 production and impact over China.
Effects of anthropogenic nitrogen input on the aquatic food webs of river ecosystem in central Japan
NASA Astrophysics Data System (ADS)
Ohte, N.; Togashi, H.; Tokuchi, N.; Yoshimura, M.; Kato, Y.; Ishikawa, N. F.; Osaka, K.; Kondo, M.; Tayasu, I.
2014-12-01
To evaluate the impact of the anthropogenic nitrogen input to the river ecosystem, we conducted the monitoring on nutrient status of river waters and food web structures of aquatic organisms. Especially, changes of sources and concentration of nitrate (NO3-) in river water were focused to evaluate the impact of anthropogenic nitrogen loadings from agricultural and residential areas. Stable nitrogen isotope ratio (δ15N) of aquatic organisms has also intensively been monitored not only to describe their food web structure, but also to detect the influences of extraneous nitrogen inputs. Field samplings an observation campaigns were conducted in the Arida river watershed located in central part of Japan at four different seasons from September 2011 to October 2012. Five observation points were set from headwaters to the point just above the brackish waters starts. Water samples for chemical analysis were taken at the observation points for each campaign. Organisms including leaf litters, benthic algae, aquatic insects, crustacean, and fishes were sampled at each point quantitatively. Results of the riverine survey utilizing 5 regular sampling points showed that δ15N of nitrate (NO3-) increased from forested upstream (˜2 ‰) to the downstream (˜7 ‰) due to the sewage loads and fertilizer effluents from agricultural area. Correspondingly the δ15N of benthic algae and aquatic insects increased toward the downstream. This indicates that primary producers of each reach strongly relied on the local N sources and it was utilized effectively in their food web. Simulation using a GIS based mixing model considering the spatial distributions of human population density and fertilizer effluents revealed that strongest impacts of N inputs was originated from organic fertilizers applied to orchards in the middle to lower parts of catchment. Differences in δ15N between primary producers and predators were 6-7 ‰ similarly at all sampling points. Food web structural analysis using food network unfolding technique based on observed δ15N suggested that the structure of nutrient pyramid did not differ significantly along the riverine positions, while the members of species in each trophic revel changed and the impact of anthropogenic N input was visible along the river.
Estuarine and marine coastlines are receiving waters for many anthropogenic substances. Concentrations of many of these contaminants have been diminished by regulatory control of effluents, but there is concern that continuing inputs (non-point sources) and contaminants contained...
AN ACCURACY ASSESSMENT OF MULTIPLE MID-ATLANTIC SUB-PIXEL IMPERVIOUS SURFACE MAPS
Anthropogenic impervious surfaces have an important relationship with non-point source pollution (NPS) in urban watersheds. The amount of impervious surface area in a watershed is a key indicator of landscape change. As a single variable, it serves to integrate a number of conc...
Anthropogenic Enrichment of Heavy Metals in Urban Dust and Possible Corresponding Sources
NASA Astrophysics Data System (ADS)
van Laaten, Neele; Merten, Dirk; Pirrung, Michael
2017-04-01
Atmospheric dust (particulate matter, PM) is regarded as a crucial factor for human health and a major environmental problem in densely populated areas. Due to anthropogenic processes like traffic, waste incineration and industry increased amounts of PM can be detected in those areas. To reduce the amounts detailed knowledge on both the composition of PM and the source contribution in a target area is needed. The latter has, to our knowledge, rarely been regarded in central Europe. Within this study, spider webs from various locations in the city of Jena (Germany), that act as natural trappers of PM, were analyzed for the contents of 27 trace elements using aqua regia digestion followed by ICP-OES and ICP-MS determinations. Aerosol-crust enrichment factors were calculated for selected elements and both a cluster analysis and a factor analysis were executed to identify sources of PM. High values for the enrichment factors clearly show an anthropogenic influence. In addition, the cluster analysis leads to a grouping of the sampling points mainly depending on the kind and volume of traffic at the corresponding locations. Five different possible sources of PM can be found by the factor analysis: Soil erosion (41% of variance), abrasion of rails (16%), tyre and break wear (16%), charcoal combustion (8%) and oil combustion (7%).
NASA Astrophysics Data System (ADS)
Kuze, A.; Suto, H.; Kataoka, F.; Shiomi, K.; Kondo, Y.; Crisp, D.; Butz, A.
2017-12-01
Atmospheric methane (CH4) has an important role in global radiative forcing of climate but its emission estimates have larger uncertainties than carbon dioxide (CO2). The area of anthropogenic emission sources is usually much smaller than 100 km2. The Thermal And Near infrared Sensor for carbon Observation Fourier-Transform Spectrometer (TANSO-FTS) onboard the Greenhouse gases Observing SATellite (GOSAT) has measured CO2 and CH4 column density using sun light reflected from the earth's surface. It has an agile pointing system and its footprint can cover 87-km2 with a single detector. By specifying pointing angles and observation time for every orbit, TANSO-FTS can target various CH4 point sources together with reference points every 3 day over years. We selected a reference point that represents CH4 background density before or after targeting a point source. By combining satellite-measured enhancement of the CH4 column density and surface measured wind data or estimates from the Weather Research and Forecasting (WRF) model, we estimated CH4emission amounts. Here, we picked up two sites in the US West Coast, where clear sky frequency is high and a series of data are available. The natural gas leak at Aliso Canyon showed a large enhancement and its decrease with time since the initial blowout. We present time series of flux estimation assuming the source is single point without influx. The observation of the cattle feedlot in Chino, California has weather station within the TANSO-FTS footprint. The wind speed is monitored continuously and the wind direction is stable at the time of GOSAT overpass. The large TANSO-FTS footprint and strong wind decreases enhancement below noise level. Weak wind shows enhancements in CH4, but the velocity data have large uncertainties. We show the detection limit of single samples and how to reduce uncertainty using time series of satellite data. We will propose that the next generation instruments for accurate anthropogenic CO2 and CH4 flux estimation have improve spatial resolution (˜1km2 ) to further enhance column density changes. We also propose adding imaging capability to monitor plume orientation. We will present laboratory model results and a sampling pattern optimization study that combines local emission source and global survey observations.
A Global Catalogue of Large SO2 Sources and Emissions Derived from the Ozone Monitoring Instrument
NASA Technical Reports Server (NTRS)
Fioletov, Vitali E.; McLinden, Chris A.; Krotkov, Nickolay; Li, Can; Joiner, Joanna; Theys, Nicolas; Carn, Simon; Moran, Mike D.
2016-01-01
Sulfur dioxide (SO2) measurements from the Ozone Monitoring Instrument (OMI) satellite sensor processed with the new principal component analysis (PCA) algorithm were used to detect large point emission sources or clusters of sources. The total of 491 continuously emitting point sources releasing from about 30 kt yr(exp -1) to more than 4000 kt yr(exp -1) of SO2 per year have been identified and grouped by country and by primary source origin: volcanoes (76 sources); power plants (297); smelters (53); and sources related to the oil and gas industry (65). The sources were identified using different methods, including through OMI measurements themselves applied to a new emission detection algorithm, and their evolution during the 2005- 2014 period was traced by estimating annual emissions from each source. For volcanic sources, the study focused on continuous degassing, and emissions from explosive eruptions were excluded. Emissions from degassing volcanic sources were measured, many for the first time, and collectively they account for about 30% of total SO2 emissions estimated from OMI measurements, but that fraction has increased in recent years given that cumulative global emissions from power plants and smelters are declining while emissions from oil and gas industry remained nearly constant. Anthropogenic emissions from the USA declined by 80% over the 2005-2014 period as did emissions from western and central Europe, whereas emissions from India nearly doubled, and emissions from other large SO2-emitting regions (South Africa, Russia, Mexico, and the Middle East) remained fairly constant. In total, OMI-based estimates account for about a half of total reported anthropogenic SO2 emissions; the remaining half is likely related to sources emitting less than 30 kt yr(exp -1) and not detected by OMI.
NASA Astrophysics Data System (ADS)
Shuler, Christopher K.; El-Kadi, Aly I.; Dulai, Henrietta; Glenn, Craig R.; Fackrell, Joseph
2017-12-01
This study presents a modeling framework for quantifying human impacts and for partitioning the sources of contamination related to water quality in the mixed-use landscape of a small tropical volcanic island. On Tutuila, the main island of American Samoa, production wells in the most populated region (the Tafuna-Leone Plain) produce most of the island's drinking water. However, much of this water has been deemed unsafe to drink since 2009. Tutuila has three predominant anthropogenic non-point-groundwater-pollution sources of concern: on-site disposal systems (OSDS), agricultural chemicals, and pig manure. These sources are broadly distributed throughout the landscape and are located near many drinking-water wells. Water quality analyses show a link between elevated levels of total dissolved groundwater nitrogen (TN) and areas with high non-point-source pollution density, suggesting that TN can be used as a tracer of groundwater contamination from these sources. The modeling framework used in this study integrates land-use information, hydrological data, and water quality analyses with nitrogen loading and transport models. The approach utilizes a numerical groundwater flow model, a nitrogen-loading model, and a multi-species contaminant transport model. Nitrogen from each source is modeled as an independent component in order to trace the impact from individual land-use activities. Model results are calibrated and validated with dissolved groundwater TN concentrations and inorganic δ15N values, respectively. Results indicate that OSDS contribute significantly more TN to Tutuila's aquifers than other sources, and thus should be prioritized in future water-quality management efforts.
NASA Astrophysics Data System (ADS)
McIver, R.; Milewski, I.; Loucks, R.; Smith, R.
2018-05-01
Far-field nutrient impacts associated with finfish aquaculture have been identified as a topic of concern for regulators, managers, scientists, and the public for over two decades but disentangling aquaculture impacts from those caused by other natural and anthropogenic sources has impeded the development of monitoring metrics and management plans. We apply a bulk, steady-state nitrogen loading model (NLM) framework to estimate the annual input of Total Dissolved Nitrogen (TDN) from point and non-point sources to the watershed surrounding Port Mouton Bay, Nova Scotia (Canada). We then use the results of the NLM together with estimates of dissolved inorganic nitrogen (DIN) loading from a sea-cage trout farm in the Bay and progressive vector diagrams to illustrate potential patterns of DIN dispersal from the trout farm. Our estimated anthropogenic nitrogen contribution to Port Mouton Bay from all terrestrial and atmospheric sources is ∼211,703 kg TDN/year with atmospheric deposition accounting for almost all (98.6%). At a stocking level of ∼400,000 rainbow trout, the Port Mouton Bay sea-cage farm increases the annual anthropogenic TDN loading to the bay by 14.4% or 30,400 kg. Depending on current flow rates, nitrogen flux from the trout farm can be more than double the background concentrations of TDN near the farm site. Although it is unlikely that nitrogen loading from this single fish farm is saturating the DIN requirements of the entire bay, progressive vector diagrams suggest that the dispersal potential may be insufficient to mitigate potential symptoms of eutrophication associated with nitrogen fluxes. We present an accessible and user-friendly tool for managers to estimate baseline nutrient loading in relation to aquaculture and our use of progressive vector diagrams illustrate a practical and simple method for characterizing potential nutrient dispersal based on local conditions and spatial scales. Our study joins numerous studies which have highlighted the need for more effective monitoring and assessment methods to improve the detection of aquaculture effects at far-field scales and to assess those effects in relation to other natural and anthropogenic factors impacting coastal habitats.
Anthropogenic heavy metals in the environment of Eurasian Arctic Nature Reserves
NASA Astrophysics Data System (ADS)
Vinogradova, Anna; Ivanova, Yulia; Karpov, Alexey
2014-05-01
The Russian Arctic Nature Reserves are situated far from the main industrial regions. In spite of this, there are anthropogenic constituents (for example, heavy metals - HM) in the environmental objects (air, water, etc.) and in food chains (plants, birds, and so on). We studied the long-range atmospheric transport of some heavy metals (such as nickel, copper, lead, arsenic, and so on) to four Nature Reserves situated near the shore of the Arctic Ocean - in the Deltas of the Pechora River (Nenets reserve), the Ob River (Gydansky reserve), the Lena River (Ust-Lensky reserve), and at Wrangel Island. The air mass trajectories to each reserve were calculated with the help of the site (www.arl.noaa.gov/ready) for each day of January, April, July, and October for the period of 2001-2010. Analyzing the spatial distributions of these trajectories we studied seasonal variations in air transport of pollution to different Russian Arctic points. Modeling the HM transport in the atmosphere was as in [1]. The main assumption is that HM are transported with submicron aerosol particles. The annual source emissions for the last decade are generalized from the data published by Roshydromet of Russia (http://www.nii-atmosphere.ru/files/PUBL/Eg_2008.doc). The main important source-regions were found for each point. Mean anthropogenic HM concentrations in air and precipitations, as well as HM fluxes onto the surface were estimated at different arctic regions. The spatial distributions of so called "potential function of pollution" were calculated and presented on the maps. These results allow to analyze the role of a real pollution source or of a planned source for each reserve. So, the influence of northern oil and gas industry may be of great importance because of its proximity to the reserves under investigation. The work was partly supported by RFBR, grant No. 14-05-00059. Authors thank the NOAA service for possibility to use their data and products. ________________ 1. Vinogradova A.A. and Ponomareva T.Ya. Atmospheric Transport of Anthropogenic Impurities to the Russian Arctic (1986-2010) // Atmospheric and Oceanic Optics. 2012. V. 25. No. 6. P. 414-422. (Engl. Transl.)
Using Rare Earth Elements (REE) to determine wind-driven soil dispersal from a point source
USDA-ARS?s Scientific Manuscript database
Although erosion of soil by water is a predictably directional process, the erosion of soil by wind is determined by wind direction on an event-wise basis. The wind-driven dispersal patterns of chemical constituents including natural soil components and anthropogenic contaminants are not well under...
Kerrigan, Jill F.; Engstrom, Daniel R.; Yee, Donald; Sueper, Charles; Erickson, Paul R.; Grandbois, Matthew; McNeill, Kristopher; Arnold, William A.
2015-01-01
Hydroxylated polybrominated diphenyl ethers (OH-BDEs) are a new class of contaminants of emerging concern, but the relative roles of natural and anthropogenic sources remain uncertain. Polybrominated diphenyl ethers (PBDEs) are used as brominated flame retardants, and they are a potential source of OH-BDEs via oxidative transformations. OH-BDEs are also natural products in marine systems. In this study, OH-BDEs were measured in water and sediment of freshwater and coastal systems along with the anthropogenic wastewater-marker compound triclosan and its photoproduct dioxin, 2,8-dichlorodibenzo-p-dioxin. The 6-OH-BDE 47 congener and its brominated dioxin (1,3,7-tribromodibenzo-p-dioxin) photoproduct were the only OH-BDE and brominated dioxin detected in surface sediments from San Francisco Bay, the anthropogenically impacted coastal site, where levels increased along a north-south gradient. Triclosan, 6-OH-BDE 47, 6-OH-BDE 90, 6-OH-BDE 99, and (only once) 6’-OH-BDE 100 were detected in two sediment cores from San Francisco Bay. The occurrence of 6-OH-BDE 47 and 1,3,7-tribromodibenzo-p-dioxin sediments in Point Reyes National Seashore, a marine system with limited anthropogenic impact, was generally lower than in San Francisco Bay surface sediments. OH-BDEs were not detected in freshwater lakes. The spatial and temporal trends of triclosan, 2,8-dichlorodibenzo-p-dioxin, OH-BDEs, and brominated dioxins observed in this study suggest that the dominant source of OH-BDEs in these systems is likely natural production, but their occurrence may be enhanced in San Francisco Bay by anthropogenic activities. PMID:26466159
NASA Astrophysics Data System (ADS)
Mekonnen, M. M.; Hoekstra, A. Y. Y.
2014-12-01
We estimated anthropogenic phosphorus (P) loads to freshwater, globally at a spatial resolution level of 5 by 5 arc minute. The global anthropogenic P load to freshwater systems from both diffuse and point sources in the period 2002-2010 was 1.5 million tonnes per year. China contributed about 30% to this global anthropogenic P load. India was the second largest contributor (8%), followed by the USA (7%), Spain and Brazil each contributing 6% to the total. The domestic sector contributed the largest share (54%) to this total followed by agriculture (38%) and industry (8%). Among the crops, production of cereals had the largest contribution to the P loads (32%), followed by fruits, vegetables, and oil crops, each contributing about 15% to the total. We also calculated the resultant grey water footprints, and relate the grey water footprints per river basin to runoff to calculate the P-related water pollution level (WPL) per catchment.
Furlong, Edward T.; Gray, James L.; Quanrud, David M.; Teske, Sondra S.; Werner, Stephen L.; Esposito, Kathleen; Marine, Jeremy; Ela, Wendell P.; Zaugg, Steven D.; Phillips, Patrick J.; Stinson, Beverley
2012-01-01
The ubiquitous presence of pharmaceuticals and other emerging contaminants, or trace organic compounds, in surface water has resulted in research and monitoring efforts to identify contaminant sources to surface waters and to better understand loadings from these sources. Wastewater treatment plant discharges have been identified as an important point source of trace organic compounds to surface water and understanding the transport and transformation of these contaminants through wastewater treatment process is essential to controlling their introduction to receiving waters.
Path-integral method for the source apportionment of photochemical pollutants
NASA Astrophysics Data System (ADS)
Dunker, A. M.
2015-06-01
A new, path-integral method is presented for apportioning the concentrations of pollutants predicted by a photochemical model to emissions from different sources. A novel feature of the method is that it can apportion the difference in a species concentration between two simulations. For example, the anthropogenic ozone increment, which is the difference between a simulation with all emissions present and another simulation with only the background (e.g., biogenic) emissions included, can be allocated to the anthropogenic emission sources. The method is based on an existing, exact mathematical equation. This equation is applied to relate the concentration difference between simulations to line or path integrals of first-order sensitivity coefficients. The sensitivities describe the effects of changing the emissions and are accurately calculated by the decoupled direct method. The path represents a continuous variation of emissions between the two simulations, and each path can be viewed as a separate emission-control strategy. The method does not require auxiliary assumptions, e.g., whether ozone formation is limited by the availability of volatile organic compounds (VOCs) or nitrogen oxides (NOx), and can be used for all the species predicted by the model. A simplified configuration of the Comprehensive Air Quality Model with Extensions (CAMx) is used to evaluate the accuracy of different numerical integration procedures and the dependence of the source contributions on the path. A Gauss-Legendre formula using three or four points along the path gives good accuracy for apportioning the anthropogenic increments of ozone, nitrogen dioxide, formaldehyde, and nitric acid. Source contributions to these increments were obtained for paths representing proportional control of all anthropogenic emissions together, control of NOx emissions before VOC emissions, and control of VOC emissions before NOx emissions. There are similarities in the source contributions from the three paths but also differences due to the different chemical regimes resulting from the emission-control strategies.
Path-integral method for the source apportionment of photochemical pollutants
NASA Astrophysics Data System (ADS)
Dunker, A. M.
2014-12-01
A new, path-integral method is presented for apportioning the concentrations of pollutants predicted by a photochemical model to emissions from different sources. A novel feature of the method is that it can apportion the difference in a species concentration between two simulations. For example, the anthropogenic ozone increment, which is the difference between a simulation with all emissions present and another simulation with only the background (e.g., biogenic) emissions included, can be allocated to the anthropogenic emission sources. The method is based on an existing, exact mathematical equation. This equation is applied to relate the concentration difference between simulations to line or path integrals of first-order sensitivity coefficients. The sensitivities describe the effects of changing the emissions and are accurately calculated by the decoupled direct method. The path represents a continuous variation of emissions between the two simulations, and each path can be viewed as a separate emission-control strategy. The method does not require auxiliary assumptions, e.g., whether ozone formation is limited by the availability of volatile organic compounds (VOC's) or nitrogen oxides (NOx), and can be used for all the species predicted by the model. A simplified configuration of the Comprehensive Air Quality Model with Extensions is used to evaluate the accuracy of different numerical integration procedures and the dependence of the source contributions on the path. A Gauss-Legendre formula using 3 or 4 points along the path gives good accuracy for apportioning the anthropogenic increments of ozone, nitrogen dioxide, formaldehyde, and nitric acid. Source contributions to these increments were obtained for paths representing proportional control of all anthropogenic emissions together, control of NOx emissions before VOC emissions, and control of VOC emissions before NOx emissions. There are similarities in the source contributions from the three paths but also differences due to the different chemical regimes resulting from the emission-control strategies.
Anthropogenic impervious surfaces have an important relationship with non-point source pollution (NPS) in urban watersheds. The amount of impervious surface area in a watershed is a key indicator of landscape change. As a single variable, it serves to intcgrate a number of concur...
NASA Astrophysics Data System (ADS)
Vela, A. V.; González, C. M.; Ynoue, R.; Rojas, N. Y.; Aristizábal, B. H.; Wahl, M.
2017-12-01
Eulerian 3-D chemistry transport models (CTM) have been widely used for the study of air quality in urban environments, becoming an essential tool for studying the impacts and dynamics of gases and aerosols on air quality. However, their use in Colombia is scarce, especially in medium-sized cities, which are experimenting a fast urban growth, increasing the risk associated with possible air pollution episodes. In the densely populated medium-sized Andean city of Manizales, Colombia - a city located on the western slopes of the central range of the Andes (urban population 368000; 2150 m.a.s.l), there is an influence of the active Nevado del Ruiz volcano, located 28 km to the southwest. This natural source emits daily gas and particle fluxes, which could influence the atmospheric chemistry of the city and neighboring towns. Hence, the zone presents a unique combination of anthropogenic and volcanic sulfur gas emissions, which affects SO2 dynamics in the urban area, influencing also in the formation of acid rain phenomenon in the city. Therefore, studies analyzing the relative contribution of anthropogenic and volcanic emission could contribute with a deep understanding about causes and dynamics of both acid rain phenomenon and ambient SO2 levels in Manizales. This work aimed to analyze the influence of anthropogenic (on-road vehicular and industrial point-sources) and volcanic sulfur emissions in SO2 atmospheric chemistry dynamics, evaluating its possible effects on acid rain profiles. Ambient SO2 levels and day-night rain samples were measured and used to analyze results obtained from the application of the fully-coupled on-line WRF-Chem model. Two high-resolution simulations were performed during two dry and wet one-week periods in 2015. Analysis of SO2 dispersion patterns and comparison with SO2 observations in the urban area were performed for three different scenarios in which natural and anthropogenic emissions were simulated separately. Results suggest that industrial point-source emissions had a higher influence in urban SO2 formation, suggesting also reasons of higher acidity levels during daytime periods, pattern obtained when comparing acid rain day-night profiles from rain samples measurements.
NASA Astrophysics Data System (ADS)
Aubrey, A. D.; Thorpe, A. K.; Christensen, L. E.; Dinardo, S.; Frankenberg, C.; Rahn, T. A.; Dubey, M.
2013-12-01
It is critical to constrain both natural and anthropogenic sources of methane to better predict the impact on global climate change. Critical technologies for this assessment include those that can detect methane point and concentrated diffuse sources over large spatial scales. Airborne spectrometers can potentially fill this gap for large scale remote sensing of methane while in situ sensors, both ground-based and mounted on aerial platforms, can monitor and quantify at small to medium spatial scales. The Jet Propulsion Laboratory (JPL) and collaborators recently conducted a field test located near Casper, WY, at the Rocky Mountain Oilfield Test Center (RMOTC). These tests were focused on demonstrating the performance of remote and in situ sensors for quantification of point-sourced methane. A series of three controlled release points were setup at RMOTC and over the course of six experiment days, the point source flux rates were varied from 50 LPM to 2400 LPM (liters per minute). During these releases, in situ sensors measured real-time methane concentration from field towers (downwind from the release point) and using a small Unmanned Aerial System (sUAS) to characterize spatiotemporal variability of the plume structure. Concurrent with these methane point source controlled releases, airborne sensor overflights were conducted using three aircraft. The NASA Carbon in Arctic Reservoirs Vulnerability Experiment (CARVE) participated with a payload consisting of a Fourier Transform Spectrometer (FTS) and an in situ methane sensor. Two imaging spectrometers provided assessment of optical and thermal infrared detection of methane plumes. The AVIRIS-next generation (AVIRIS-ng) sensor has been demonstrated for detection of atmospheric methane in the short wave infrared region, specifically using the absorption features at ~2.3 μm. Detection of methane in the thermal infrared region was evaluated by flying the Hyperspectral Thermal Emission Spectrometer (HyTES), retrievals which interrogate spectral features in the 7.5 to 8.5 μm region. Here we discuss preliminary results from the JPL activities during the RMOTC controlled release experiment, including capabilities of airborne sensors for total columnar atmospheric methane detection and comparison to results from ground measurements and dispersion models. Potential application areas for these remote sensing technologies include assessment of anthropogenic and natural methane sources over wide spatial scales that represent significant unconstrained factors to the global methane budget.
[Anthropogenic ammonia emission inventory and characteristics in the Pearl River Delta Region].
Yin, Sha-sha; Zheng, Jun-yu; Zhang, Li-jun; Zhong, Liu-ju
2010-05-01
Based on the collected activity data and emission factors of anthropogenic ammonia sources, a 2006-based anthropogenic ammonia emission inventory was developed for the Pearl River Delta (PRD) region by source categories and cities with the use of appropriate estimation methods. The results show: (1) the total NH3 emission from anthropogenic sources in the PRD region was 194. 8 kt; (2) the agriculture sources were major contributors of anthropogenic ammonia sources, in which livestock sources shared 62.1% of total NH3 emission and the contribution of application of nitrogen fertilizers was 21.7%; (3) the broiler was the largest contributor among the livestock sources, accounting for 43.4% of the livestock emissions, followed by the hog with a contribution of 32.1%; (4) Guangzhou was the largest ammonia emission city in the PRD region, and then Jiangmen, accounting for 23.4% and 19.1% of total NH3 emission in the PRD region respectively, with major sources as livestock sources and application of nitrogen fertilizers.
An integrated approach to assess heavy metal source apportionment in peri-urban agricultural soils.
Huang, Ying; Li, Tingqiang; Wu, Chengxian; He, Zhenli; Japenga, Jan; Deng, Meihua; Yang, Xiaoe
2015-12-15
Three techniques (Isotope Ratio Analysis, GIS mapping, and Multivariate Statistical Analysis) were integrated to assess heavy metal pollution and source apportionment in peri-urban agricultural soils. The soils in the study area were moderately polluted with cadmium (Cd) and mercury (Hg), lightly polluted with lead (Pb), and chromium (Cr). GIS Mapping suggested Cd pollution originates from point sources, whereas Hg, Pb, Cr could be traced back to both point and non-point sources. Principal component analysis (PCA) indicated aluminum (Al), manganese (Mn), nickel (Ni) were mainly inherited from natural sources, while Hg, Pb, and Cd were associated with two different kinds of anthropogenic sources. Cluster analysis (CA) further identified fertilizers, waste water, industrial solid wastes, road dust, and atmospheric deposition as potential sources. Based on isotope ratio analysis (IRA) organic fertilizers and road dusts accounted for 74-100% and 0-24% of the total Hg input, while road dusts and solid wastes contributed for 0-80% and 19-100% of the Pb input. This study provides a reliable approach for heavy metal source apportionment in this particular peri-urban area, with a clear potential for future application in other regions. Copyright © 2015 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Hopkins, F. M.; Duren, R. M.; Miller, C. E.; Aubrey, A. D.; Falk, M.; Holland, L.; Hook, S. J.; Hulley, G. C.; Johnson, W. R.; Kuai, L.; Kuwayama, T.; Lin, J. C.; Thorpe, A. K.; Worden, J. R.; Lauvaux, T.; Jeong, S.; Fischer, M. L.
2015-12-01
Methane is an important atmospheric pollutant that contributes to global warming and tropospheric ozone production. Methane mitigation could reduce near term climate change and improve air quality, but is hindered by a lack of knowledge of anthropogenic methane sources. Recent work has shown that methane emissions are not evenly distributed in space, or across emission sources, suggesting that a large fraction of anthropogenic methane comes from a few "super-emitters." We studied the distribution of super-emitters in California's southern San Joaquin Valley, where elevated levels of atmospheric CH4 have also been observed from space. Here, we define super-emitters as methane plumes that could be reliably detected (i.e., plume observed more than once in the same location) under varying wind conditions by airborne thermal infrared remote sensing. The detection limit for this technique was determined to be 4.5 kg CH4 h-1 by a controlled release experiment, corresponding to column methane enhancement at the point of emissions greater than 20% above local background levels. We surveyed a major oil production field, and an area with a high concentration of large dairies using a variety of airborne and ground-based measurements. Repeated airborne surveys (n=4) with the Hyperspectral Thermal Emission Spectrometer revealed 28 persistent methane plumes emanating from oil field infrastructure, including tanks, wells, and processing facilities. The likelihood that a given source type was a super-emitter varied from roughly 1/3 for processing facilities to 1/3000 for oil wells. 11 persistent plumes were detected in the dairy area, and all were associated with wet manure management. The majority (11/14) of manure lagoons in the study area were super-emitters. Comparing to a California methane emissions inventory for the surveyed areas, we estimate that super-emitters comprise a minimum of 9% of inventoried dairy emissions, and 13% of inventoried oil emissions in this region.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Schulz, H.M.
The Baltic Sea (Central Europe) is surrounded by coastal regions with long histories of industrialization. The heavy metal profiles in the sediments in the center of the Arkona Basin, one of the depressions of the southern Baltic Sea area, clearly reflect the historical anthropogenic influence. The Arkona Basin-is the final sink for materials derived from the Oder river which drains a highly polluted industrial area of Eastern Europe. Surficial muddy sediments from a close-meshed field of sampling-points were analyzed for distribution patterns of aliphatics and quantities and ratios of selected polycyclic aromatic hydrocarbons (PAH). These compounds are thought to reflectmore » anthropogenic pollution related to emissions from traffic, heating, etc. We use these marker substances to test if the basin sediments reflect riverine input, and if additional sources can be identified.« less
An unexpected truth: increasing nitrate loading can decrease nitrate export from watersheds
NASA Astrophysics Data System (ADS)
Askarizadeh Bardsiri, A.; Grant, S. B.; Rippy, M.
2015-12-01
The discharge of anthropogenic nitrate (e.g., from partially treated sewage, return flows from agricultural irrigation, and runoff from animal feeding operations) to streams can negatively impact both human and ecosystem health. Managing these many point and non-point sources to achieve some specific end-point—for example, reducing the annual mass of nitrate exported from a watershed—can be a challenge, particularly in rapidly growing urban areas. Adding to this complexity is the fact that streams are not inert: they too can add or remove nitrate through assimilation (e.g., by stream-associated plants and animals) and microbially-mediated biogeochemical reactions that occur in streambed sediments (e.g., respiration, ammonification, nitrification, denitrification). By coupling a previously published correlation for in-stream processing of nitrate [Mulholland et al., Nature, 2008, 452, 202-205] with a stream network model of the Jacksons Creek watershed (Victoria, Australia) I demonstrate that managing anthropogenic sources of stream nitrate without consideration of in-stream processing can result in a number of non-intuitive "surprises"; for example, wastewater effluent discharges that increase nitrate loading but decrease in-stream nitrate concentrations can reduce the mass of nitrate exported from a watershed.
NASA Astrophysics Data System (ADS)
Howard, Meredith D. A.; Kudela, Raphael M.; McLaughlin, Karen
2017-02-01
Anthropogenic nutrient inputs are one of the most important factors contributing to eutrophication of coastal waters. Coastal upwelling regions are naturally highly variable, exhibiting faster flushing and lower retention times than estuarine systems. As such, these regions are considered more resilient to anthropogenic influences than other coastal waters. Recent studies have shown our perception of the sustainability of these systems may be flawed and that anthropogenic nutrients can have an impact at local and regional spatial scales within these larger upwelling ecosystems. Maintenance of an outfall pipe discharging wastewater effluent to the Southern California Bight (SCB) provided an opportunity to study effects of anthropogenic nutrient inputs on a near-shore coastal ecosystem. The diversion of wastewater effluent from a primary, offshore outfall to a secondary, near-shore outfall set up a large-scale, in situ experiment allowing researchers to track the fate of wastewater plumes as they were "turned off" in one area and "turned on" in another. In this introduction to a special issue, we synthesize results of one such wastewater diversion conducted by the Orange County Sanitation District (OCSD) during fall 2012. Anthropogenic nitrogen (N) from point-source discharges altered biogeochemical cycling and the community composition of bacteria and phytoplankton. Nitrification of ammonium to nitrate in wastewater effluent close to outfalls constituted a significant source of N utilized by the biological community that should be considered in quantifying "new" production. The microbial-loop component of the plankton community played a significant role, exemplified by a large response of heterotrophic bacteria to wastewater effluent that resulted in nutrient immobilization within the bacterial food web. This response, combined with the photosynthetic inhibition of phytoplankton due to disinfection byproducts, suppressed phytoplankton responses. Our findings have ramifications for future studies and regulatory monitoring, emphasizing the need to consider chemical and biological responses to wastewater effluent in assessing effects of anthropogenic nutrient inputs on urbanized coastal ecosystems.
NASA Astrophysics Data System (ADS)
Ehret, G.; Amediek, A.; Wirth, M.; Fix, A.; Kiemle, C.; Quatrevalet, M.
2016-12-01
We report on a new method and on the first demonstration to quantify emission rates from strong greenhouse gas (GHG) point sources using airborne Integrated Path Differential Absorption (IPDA) Lidar measurements. In order to build trust in the self-reported emission rates by countries, verification against independent monitoring systems is a prerequisite to check the reported budget. A significant fraction of the total anthropogenic emission of CO2 and CH4 originates from localized strong point sources of large energy production sites or landfills. Both are not monitored with sufficiently accuracy by the current observation system. There is a debate whether airborne remote sensing could fill in the gap to infer those emission rates from budgeting or from Gaussian plume inversion approaches, whereby measurements of the GHG column abundance beneath the aircraft can be used to constrain inverse models. In contrast to passive sensors, the use of an active instrument like CHARM-F for such emission verification measurements is new. CHARM-F is a new airborne IPDA-Lidar devised for the German research aircraft HALO for the simultaneous measurement of the column-integrated dry-air mixing ratio of CO2 and CH4 commonly denoted as XCO2 und XCH4, respectively. It has successfully been tested in a serious of flights over Central Europe to assess its performance under various reflectivity conditions and in a strongly varying topography like the Alps. The analysis of a methane plume measured in crosswind direction of a coal mine ventilation shaft revealed an instantaneous emission rate of 9.9 ± 1.7 kt CH4 yr-1. We discuss the methodology of our point source estimation approach and give an outlook on the CoMet field experiment scheduled in 2017 for the measurement of anthropogenic and natural GHG emissions by a combination of active and passive remote sensing instruments on research aircraft.
NASA Astrophysics Data System (ADS)
Longmire, P.; Dale, M.; Granzow, K.; Yanicak, S. M.
2014-12-01
Los Alamos National Laboratory (LANL) is an operating nuclear site that has released treated effluents from three plutonium-processing facilities since the mid 1940s. The radioisotope 129I (T1/2 = 15.7 Myrs) derived from235U and 239Pu processing at LANL is locally detected in groundwater above background concentrations. This isotope provides a unique tracer for groundwater investigations conducted at LANL that helps to identify source releases linked to groundwater-flow paths in aquifers subject to binary and ternary mixing of natural- and industrial-derived waters containing chromate and other chemicals. Bromide, chlorate, chloride, nitrate, perchlorate, sulfate, and tritium were associated with multiple outfalls at LANL and, therefore, do not provide unique chemical signatures identifying a specific point of release or source. Natural and anthropogenic ratios of 129I/127I measured in groundwater samples collected at LANL were quantified using accelerator mass spectrometry at Purdue Rare Isotope Measurement Laboratory, Purdue University. Anthropogenic ratios of 129I/127I range from 1,531 X 10-15 to 10,323 X 10-15 within perched-intermediate groundwater present in volcanoclastic and basalt aquifers (210 - 216 m depth). Anthropogenic ratios of 129I/127I range from 359 X 10-15 to 4,350 X 10-15 within the regional aquifer (280 m depth) consisting of volcanoclastic sediments of variable hydraulic properties. Local background ratios of 129I/127I have a narrow range of 171 X 10-15 to 378 X 10-15 in the regional aquifer. Dissolved iodide measured in groundwater at LANL is stable dominantly as iodate. Background concentrations of dissolved iodate (0.1 to 33.2 nM) are less variable compared to anthropogenic iodate (8.0 to 246 nM) in groundwater at the site. Variability in concentrations of anthropogenic iodate is controlled by heterogeneous source releases of iodate over time and non-uniform mixing of groundwater in the different aquifers.
NASA Astrophysics Data System (ADS)
Grigg, R. W.
1995-11-01
The effects of natural and anthropogenic stress need to be separated before coral reef ecosystems can be effectively managed. In this paper, a 25 year case history of coral reefs in an urban embayment (Mamala Bay) off Honolulu, Hawaii is described and differences between natural and man-induced stress are distinguished. Mamala Bay is a 30 km long shallow coastal bay bordering the southern (leeward) shore of Oahu and the city of Honolulu in the Hawaiian Islands. During the last 25 years, this area has been hit by two magnitude 5 hurricane events (winds > 240 km/h) generating waves in excess of 7.5 m. Also during this period, two large sewer outfalls have discharged up to 90 million gallons per day (mgd) or (360 × 106 L/day) of point source pollution into the bay. Initially the discharge was raw sewage, but since 1977 it has received advanced primary treatment. Non-point source run-off from the Honolulu watershed also enters the bay on a daily basis. The results of the study show that discharge of raw sewage had a serious but highly localized impact on shallow (˜10 m) reef corals in the bay prior to 1977. After 1977, when treatment was upgraded to the advanced primary level and outfalls were extended to deep water (> 65 m), impacts to reef corals were no longer significant. No measurable effects of either point or non-point source pollution on coral calcification, growth, species composition, diversity or community structure related to pollution can now be detected. Conversely the effects of hurricane waves in 1982 and 1992 together caused major physical destruction to the reefs. In 1982, average coral cover of well-developed offshore reefs dropped from 60-75% to 5-15%. Only massive species in high relief areas survived. Today, recovery is occurring, and notwithstanding major future disturbance events, long-term biological processes should eventually return the coral ecosystems to a more mature successional stage. This case history illustrates the complex nature of the cumulative effects of natural and anthropogenic stress on coral reefs and the need for a long-term data base before the status of a coral reef can be properly interpreted.
The SE US and the Amazon have large sources of biogenic VOCs, varying anthropogenic pollution impacts, and often poor organic aerosol (OA) model performance. Recent results on the sources, properties, aging, and impact of anthropogenic pollution on OA and secondary OA (SOA) over ...
Neill, Aaron James; Tetzlaff, Doerthe; Strachan, Norval James Colin; Hough, Rupert Lloyd; Avery, Lisa Marie; Watson, Helen; Soulsby, Chris
2018-01-15
An 11year dataset of concentrations of E. coli at 10 spatially-distributed sites in a mixed land-use catchment in NE Scotland (52km 2 ) revealed that concentrations were not clearly associated with flow or season. The lack of a clear flow-concentration relationship may have been due to greater water fluxes from less-contaminated headwaters during high flows diluting downstream concentrations, the importance of persistent point sources of E. coli both anthropogenic and agricultural, and possibly the temporal resolution of the dataset. Point sources and year-round grazing of livestock probably obscured clear seasonality in concentrations. Multiple linear regression models identified potential for contamination by anthropogenic point sources as a significant predictor of long-term spatial patterns of low, average and high concentrations of E. coli. Neither arable nor pasture land was significant, even when accounting for hydrological connectivity with a topographic-index method. However, this may have reflected coarse-scale land-cover data inadequately representing "point sources" of agricultural contamination (e.g. direct defecation of livestock into the stream) and temporal changes in availability of E. coli from diffuse sources. Spatial-stream-network models (SSNMs) were applied in a novel context, and had value in making more robust catchment-scale predictions of concentrations of E. coli with estimates of uncertainty, and in enabling identification of potential "hot spots" of faecal contamination. Successfully managing faecal contamination of surface waters is vital for safeguarding public health. Our finding that concentrations of E. coli could not clearly be associated with flow or season may suggest that management strategies should not necessarily target only high flow events or summer when faecal contamination risk is often assumed to be greatest. Furthermore, we identified SSNMs as valuable tools for identifying possible "hot spots" of contamination which could be targeted for management, and for highlighting areas where additional monitoring could help better constrain predictions relating to faecal contamination. Copyright © 2017 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Cao, D.; Cao, W.; Yu, K.; Wu, G.; Yang, J.; Su, X.; Wang, F.
2017-05-01
Coral reefs have suffered remarkable declines worldwide. Nutrient overenrichment is considered to be one of the primary local causes. The Luhuitou fringing reef in southern China is a well-known tourist destination that is subject to enormous coastal renovation. The mean δ13C, δ15N value, and carbon over nitrogen ratio (C/N) of particulate organic matter were -21.56 ± 1.94‰, 7.04 ± 3.81‰, and 5.81 ± 1.86, respectively, suggesting mixed sources of carbon and nitrogen. The IsoError calculations suggested that marine phytoplankton and marine benthic algae dominated the majority of carbon sources, while anthropogenic and terrestrial organic nitrogen dominated the nitrogen sources. A tendency toward greater terrestrial detritus and anthropogenic-derived discharges was found during dry seasons and greater marine-derived organic matter during wet seasons. These results demonstrated the existence of anthropogenic influences and high dissolved inorganic nitrogen concentrations and C/N ratios. Anthropogenic nutrient discharge moderated nitrogen limitation, whereas phosphorus became more important to the reef ecosystem. Despite the marine carbon sources dominated, freshwater and terrestrial-derived organic carbon sources were also very important. Meanwhile, anthropogenic and terrestrial organic nitrogen sources were dominant. Therefore, pollution from more extensive region and anthropogenic activities from riverine sewage discharges adjacent to reefs should be focused to effectively reduce human-derived nutrients on reefs.
Simulating the Earth System Response to Negative Emissions
NASA Astrophysics Data System (ADS)
Jackson, R. B.; Milne, J.; Littleton, E. W.; Jones, C.; Canadell, J.; Peters, G. P.; van Vuuren, D.; Davis, S. J.; Jonas, M.; Smith, P.; Ciais, P.; Rogelj, J.; Torvanger, A.; Shrestha, G.
2016-12-01
The natural carbon sinks of the land and oceans absorb approximately half the anthropogenic CO2 emitted every year. The CO2 that is not absorbed accumulates in the Earth's atmosphere and traps the suns rays causing an increase in the global mean temperature. Removing this left over CO2 using negative emissions technologies (NETs) has been proposed as a strategy to lessen the accumulating CO2 and avoid dangerous climate change. Using CMIP5 Earth system model simulations this study assessed the impact on the global carbon cycle, and how the Earth system might respond, to negative emissions strategies applied to low emissions scenarios, over different times horizons from the year 2000 to 2300. The modeling results suggest that using NETs to remove atmospheric CO2 over five 50-year time horizons has varying effects at different points in time. The effects of anthropogenic and natural sources and sinks, can result in positive or negative changes in atmospheric CO2 concentration. Results show that historic emissions and the current state of the Earth System have impacts on the behavior of atmospheric CO2, as do instantaneous anthropogenic emissions. Indeed, varying background scenarios seemed to have a greater effect on atmospheric CO2 than the actual amount and timing of NETs. These results show how NETs interact with the physical climate-carbon cycle system and highlight the need for more research on earth-system dynamics as they relate to carbon sinks and sources and anthropogenic perturbations.
NASA Astrophysics Data System (ADS)
Millet, Dylan B.; Goldstein, Allen H.; Holzinger, Rupert; Williams, Brent J.; Allan, James D.; Jimenez, José L.; Worsnop, Douglas R.; Roberts, James M.; White, Allen B.; Hudman, Rynda C.; Bertschi, Isaac T.; Stohl, Andreas
2006-12-01
We present a factor analysis-based method for differentiating air masses on the basis of source influence and apply the method to a broad suite of trace gas and aerosol measurements collected at Chebogue Point, Nova Scotia, during the summer of 2004 to characterize the chemical composition of atmospheric outflow from eastern North America. CO, ozone, and aerosol mass were elevated by 30%, 56%, and more than 300% at Chebogue Point during U.S. outflow periods. Organic aerosol mass was highest during U.S. pollution events, but made up the largest fraction (70%) of the total aerosol during periods of primary and especially secondary biogenic influence, indicating the importance of both anthropogenic and biogenic organic aerosol. Anthropogenic and oxygenated volatile organic compounds account for the bulk of the gas-phase organic carbon under most conditions; however, biogenic compounds are important in terms of chemical reactivity. Biogenic emissions thus have a significant impact on the chemistry of air masses downwind of the polluted northeastern United States. Using output from a global 3-D model of atmospheric composition (GEOS-Chem), we estimate that CO directly emitted from U.S. pollution sources makes up 28% of the total CO observed at Chebogue Point during U.S. outflow events and 19% at other times, although more work is needed to improve U.S. emission estimates for CO and other pollutants. We conclude that the effects of North American pollution on the chemistry of the western North Atlantic boundary layer are pervasive and not restricted to particular events.
Campbell, J. E.; Whelan, Mary; Seibt, U.; ...
2015-04-16
Carbonyl sulfide (COS) has recently emerged as an atmospheric tracer of gross primary production. All modeling studies of COS air-monitoring data rely on a climatological anthropogenic inventory that does not reflect present conditions or support interpretation of ice core and firn trends. Here we develop a global anthropogenic inventory for the years 1850 to 2013 based on new emission measurements and material-specific data. By applying methods from a recent regional inventory to global data, we find that the anthropogenic source is similar in magnitude to the plant sink, confounding carbon cycle applications. However, a material-specific approach results in a currentmore » anthropogenic source that is only one third of plant uptake and is concentrated in Asia, supporting carbon cycle applications of global air-monitoring data. As a result, changes in the anthropogenic source alone cannot explain the century-scale mixing ratio growth, which suggests that ice and firn data may provide the first global history of gross primary production.« less
DOE Office of Scientific and Technical Information (OSTI.GOV)
Zumkehr, Andrew; Hilton, Timothy W.; Whelan, Mary
Carbonyl sulfide (COS or OCS), the most abundant sulfur containing gas in the troposphere, has recently emerged as a potentially important atmospheric tracer for the carbon cycle. Atmospheric inverse modeling studies may be able to use existing tower, airborne, and satellite observations of COS to infer information about photosynthesis. However, such analysis relies on gridded anthropogenic COS source estimates that are largely based on industry activity data from over three decades ago. Here we use updated emission factor data and industry activity data to develop a gridded inventory with a 0.1 degree resolution for the U.S. domain. The inventory includesmore » the primary anthropogenic COS sources including direct emissions from the coal and aluminum industries as well as indirect sources from industrial carbon disulfide emissions. Compared to the previously published inventory, we found that the total anthropogenic source (direct and indirect) is 47% smaller. Using this new gridded inventory to drive the STEM/WRF atmospheric transport model, we found that the anthropogenic contribution to COS variation in the troposphere is small relative to the biosphere influence, which is encouraging of carbon cycle applications in this region. Additional anthropogenic sectors with highly uncertain emission factors require further field measurements.« less
Kikuchi, Ryunosuke; Gorbacheva, Tamara T
2009-06-01
The Arctic holds large stores of minerals, and extracted materials are provided to the world's economy; in this sense, the Arctic issue associated with mining is not local but global. In a part of the Arctic region (the Kola Peninsula, 66-70 degrees N and 28-41 degrees E), metal levels are generally elevated in the lake sediment. There is a question as to what results in elevated metal levels-a natural process (naturally abundant minerals) or an anthropogenic process (mining and metallurgy). In terms of solving this question, Staroe lake located on the Kola Peninsula was researched as a case study. The following parameters were determined in relation with Staroe lake: (1) the current quality of the lake's water-each 1,000-ml sample was collected at a surface point and a deep point (near the bottom layer), and the collected samples were directly analyzed after filtration; (2) atmospheric bulk deposition-bulk deposition was collected using a set of three rainwater samplers near the lake. In addition, bulk deposition was collected in a background site (250 km to the southwest of the smelter complex) as a reference; and (3) sediment profile (plus principal component analysis)-lake-bottom sediment was collected by an open-gravimetric column sampler equipped with an automatic diaphragm. After collection, the sample columns were cut at a 1-cm interval for analysis. Eigenvalues and variances by factor were calculated from the correlation coefficients. The obtained data show that (1) naturally poor elements (Cu, Ni, Si, and SO(4) (2-)) dominantly influence the lake's water quality; (2) they are transported from the anthropogenic sources to the study lake through the atmospheric pathway; (3) mainly the contents of Cu, Ni, Sr, and Ca have influenced the sediment quality since the 1950s, corresponding to the industrial movement; and (4) Cu, Ni, and Sr originate from an anthropogenic source (smelter), and Ca originates from both natural and anthropogenic sources. As compared with the Russian standard (San Pin 2.1.980-00), the contents of NO(3) (-) (50.3 +/- 0.1 mg l(-1)) and particulates (2.3 +/- 0.2 mg l(-1)) exceeded the standard levels (0.7 mg l(-1) NO(3) (-) and 45 mg l(-1) particulates); Staroe lake may be slightly contaminated. However, the contamination factor (comparison with the background data) implies that Staroe lake is considerably contaminated. There is a strong possibility that fine overburden detritus (<0.1 mm diameter) may be transported from an open pit to the study lake by natural forces such as wind. Although it is difficult to suppose that one factor dominantly affects the sediment quality, it follows from a factor analysis that factors 1 and 2 account for about 70% of the total variance: Factor 1 is the most dominant, and factor 2 is the second most dominant in the variability of sediment quality. It is considered that Cu, Sr, and Ni in factor 1 originate from anthropogenic sources because they are poor in sediment rocks. The field survey conducted in Staroe lake can give the following answers to the key objectives: (1) The present water quality is affected by Cu, Ni, Si, and SO(4) (2-) in light of the contamination factor, and these elements originate from anthropogenic sources (the smelter and the open pit) and are transported to the lake through the atmospheric pathway; (2) the sediment profile and statistic analysis show that the lake quality has been influenced by deposition of metals since the 1950s; and (3) Cu, Ni, Sr, and Ca have influenced the sediment quality in light of the most dominant factor-Cu, Ni, and Sr originate from an anthropogenic source, whereas Ca comes from both natural and anthropogenic sources. The presented lake survey shows that the dispersion of human-related pollutants via the atmospheric pathway takes place in the Arctic region. If the current pollution continues without countermeasures, the high-latitude environment may lose its original characteristics; hence, this subject is important when considering how to implement a wide range of environmental protection measures in the Arctic.
Pan, Huiyun; Lu, Xinwei; Lei, Kai
2017-12-31
A detailed investigation was conducted to study heavy metal contamination in road dust from four regions of Xi'an, Northwest China. The concentrations of eight heavy metals Co, Cr, Cu, Mn, Ni, Pb, Zn and V were determined by X-Ray Fluorescence. The mean concentrations of these elements were: 30.9mgkg -1 Co, 145.0mgkg -1 Cr, 54.7mgkg -1 Cu, 510.5mgkg -1 Mn, 30.8mgkg -1 Ni, 124.5mgkg -1 Pb, 69.6mgkg -1 V and 268.6mgkg -1 Zn. There was significant enrichment of Pb, Zn, Co, Cu and Cr based on geo-accumulation index value. Multivariate statistical analysis showed that levels of Cu, Pb, Zn, Co and Cr were controlled by anthropogenic activities, while levels of Mn, Ni and V were associated with natural sources. Principle component analysis and multiple linear regression were applied to determine the source apportionment. The results showed that traffic was the main source with a percent contribution of 53.4%. Natural sources contributed 26.5%, and other anthropogenic pollution sources contributed 20.1%. Clear heavy metal pollution hotspots were identified by GIS mapping. The location of point pollution sources and prevailing wind direction were found to be important factors in the spatial distribution of heavy metals. Copyright © 2017 Elsevier B.V. All rights reserved.
Poerschmann, Juergen; Koschorreck, Matthias; Górecki, Tadeusz
2017-02-01
Natural neutralization of acidic mining lakes is often limited by organic matter. The knowledge of the sources and degradability of organic matter is crucial for understanding alkalinity generation in these lakes. Sediments collected at different depths (surface sediment layer from 0 to 1 cm and deep sediment layer from 4 to 5cm) from an acidic mining lake were studied in order to characterize sedimentary organic matter based on neutral signature markers. Samples were exhaustively extracted, subjected to pre-chromatographic derivatizations and analyzed by GC/MS. Herein, molecular distributions of diagnostic alkanes/alkenes, terpenes/terpenoids, polycyclic aromatic hydrocarbons, aliphatic alcohols and ketones, sterols, and hopanes/hopanoids were addressed. Characterization of the contribution of natural vs. anthropogenic sources to the sedimentary organic matter in these extreme environments was then possible based on these distributions. With the exception of polycyclic aromatic hydrocarbons, combined concentrations across all marker classes proved higher in the surface sediment layer as compared to those in the deep sediment layer. Alkane and aliphatic alcohol distributions pointed to predominantly allochthonous over autochthonous contribution to sedimentary organic matter. Sterol patterns were dominated by phytosterols of terrestrial plants including stigmasterol and β-sitosterol. Hopanoid markers with the ββ-biohopanoid "biological" configuration were more abundant in the surface sediment layer, which pointed to higher bacterial activity. The pattern of polycyclic aromatic hydrocarbons pointed to prevailing anthropogenic input. Pyrolytic makers were likely to due to atmospheric deposition from a nearby former coal combustion facility. The combined analysis of the array of biomarkers provided new insights into the sources and transformations of organic matter in lake sediments. Copyright © 2016 Elsevier B.V. All rights reserved.
Anthropogenic combustion iron as a complex climate forcer.
Matsui, Hitoshi; Mahowald, Natalie M; Moteki, Nobuhiro; Hamilton, Douglas S; Ohata, Sho; Yoshida, Atsushi; Koike, Makoto; Scanza, Rachel A; Flanner, Mark G
2018-04-23
Atmospheric iron affects the global carbon cycle by modulating ocean biogeochemistry through the deposition of soluble iron to the ocean. Iron emitted by anthropogenic (fossil fuel) combustion is a source of soluble iron that is currently considered less important than other soluble iron sources, such as mineral dust and biomass burning. Here we show that the atmospheric burden of anthropogenic combustion iron is 8 times greater than previous estimates by incorporating recent measurements of anthropogenic magnetite into a global aerosol model. This new estimation increases the total deposition flux of soluble iron to southern oceans (30-90 °S) by 52%, with a larger contribution of anthropogenic combustion iron than dust and biomass burning sources. The direct radiative forcing of anthropogenic magnetite is estimated to be 0.021 W m -2 globally and 0.22 W m -2 over East Asia. Our results demonstrate that anthropogenic combustion iron is a larger and more complex climate forcer than previously thought, and therefore plays a key role in the Earth system.
NASA Astrophysics Data System (ADS)
Yang, Junhua; Kang, Shichang; Ji, Zhenming; Chen, Deliang
2018-01-01
Black carbon (BC) in snow/ice induces enhanced snow and glacier melting. As over 60% of atmospheric BC is emitted from anthropogenic sources, which directly impacts the distribution and concentration of BC in snow/ice, it is essential to assess the origin of anthropogenic BC transported to the Tibetan Plateau (TP) where there are few direct emissions attributable to local human activities. In this study, we used a regional climate-atmospheric chemistry model and a set of BC scenarios for quantitative evaluation of the impact of anthropogenic BC from various sources and its climate effects over the TP in 2013. The results showed that the model performed well in terms of climatology, aerosol optical properties, and near-surface concentrations, which indicates that this modeling framework is appropriate to characterize anthropogenic BC source-receptor relationships over the TP. The simulated surface concentration associated with the anthropogenic sources showed seasonal differences. In the monsoon season, the contribution of anthropogenic BC was less than in the nonmonsoon season. In the nonmonsoon season, westerly winds prevailed and transported BC from central Asia and north India to the western TP. In the monsoon season, BC aerosol was transported to the middle-upper troposphere over the Indo-Gangetic Plain and crossed the Himalayas via southwesterly winds. The majority of anthropogenic BC over the TP was transported from South Asia, which contributed to 40%-80% (mean of 61.3%) of surface BC in the nonmonsoon season, and 10%-50% (mean of 19.4%) in the monsoon season. For the northeastern TP, anthropogenic BC from eastern China accounted for less than 10% of the total in the nonmonsoon season but can be up to 50% in the monsoon season. Averaged over the TP, the eastern China anthropogenic sources accounted for 6.2% and 8.4% of surface BC in the nonmonsoon and monsoon seasons, respectively. The anthropogenic BC induced negative radiative forcing and cooling effects at the near surface over the TP.
NASA Astrophysics Data System (ADS)
Zhou, Feng; Guo, Huaicheng; Liu, Lei
2007-10-01
Based on ten heavy metals collected twice annually at 59 sites from 1998 to 2004, enrichment factors (EFs), principal component analysis (PCA) and multivariate linear regression of absolute principal component scores (MLR-APCS) were used in identification and source apportionment of the anthropogenic heavy metals in marine sediment. EFs with Fe as a normalizer and local background as reference values was properly tested and suitable in Hong Kong, and Zn, Ni, Pb, Cu, Cd, Hg and Cr mainly originated from anthropogenic sources, while Al, Mn and Fe were derived from rocks weathering. Rotated PCA and GIS mapping further identified two types of anthropogenic sources and their impacted regions: (1) electronic industrial pollution, riparian runoff and vehicle exhaust impacted the entire Victoria Harbour, inner Tolo Harbour, Eastern Buffer, inner Deep Bay and Cheung Chau; and (2) discharges from textile factories and paint, influenced Tsuen Wan Bay and Kwun Tong typhoon shelter and Rambler Channel. In addition, MLR-APCS was successfully introduced to quantitatively determine the source contributions with uncertainties almost less than 8%: the first anthropogenic sources were responsible for 50.0, 45.1, 86.6, 78.9 and 87.5% of the Zn, Pb, Cu, Cd and Hg, respectively, whereas 49.9% of the Ni and 58.4% of the Cr came from the second anthropogenic sources.
Osmium isotopes demonstrate distal transport of contaminated sediments in Chesapeake Bay
Helz, G.R.; Adelson, J.M.; Miller, C.V.; Cornwell, J.C.; Hill, J.M.; Horan, M.; Walker, R.J.
2000-01-01
Because the isotopic composition of anthropogenic Os is normally distinctive in comparison to continental crust and is precisely measurable, this platinum-group element is attractive as a tracer of transport pathways for contaminated sediments in estuaries. Evidence herein and elsewhere suggest that biomedical research institutions are the chief source of anthropogenic Os. In the Chesapeake Bay region, uncontaminated sediments bear a crustal 187Os/188Os signature of 0.73 ?? 0.10. Slightly higher 187Os/188Os ratios occur in Re-rich Coastal Plain deposits due to post- Miocene 187Re decay. The upper Susquehanna Basin yields sediments also with higher 187Os/188Os. Beginning in the late 1970s, this signal was overprinted by a low 187Os/188Os (anthropogenic) source in the lower Susquehanna Basin. In the vicinity of Baltimore, which is a major center of heavy industry as well as biomedical research, anthropogenic Os has been found only in sediments impacted by the principal wastewater treatment plant. Surprisingly, a mid-Bay site distant from anthropogenic sources contains the strongest anthropogenic Os signal in the data set, having received anthropogenic Os sporadically since the mid-20th Century. Transport of particles to this site overrode the northward flowing bottom currents. Finding anthropogenic Os at this site cautions that other particle-borne substances, including hazardous ones, could be dispersed broadly in this estuary.Because the isotopic composition of anthropogenic Os is normally distinctive in comparison to continental crust and is precisely measurable, this platinum-group element is attractive as a tracer of transport pathways for contaminated sediments in estuaries. Evidence herein and elsewhere suggest that biomedical research institutions are the chief source of anthropogenic Os. In the Chesapeake Bay region, uncontaminated sediments bear a crustal 187Os/188Os signature of 0.73 ?? 0.10. Slightly higher 187Os/188Os ratios occur in Re-rich Coastal Plain deposits due to post-Miocene 187Re decay. The upper Susquehanna Basin yields sediments also with higher 187Os/188Os. Beginning in the late 1970s, this signal was overprinted by a low 187Os/188Os (anthropogenic) source in the lower Susquehanna Basin. In the vicinity of Baltimore, which is a major center of heavy industry as well as biomedical research, anthropogenic Os has been found only in sediments impacted by the principal wastewater treatment plant. Surprisingly, a mid-Bay site distant from anthropogenic sources contains the strongest anthropogenic Os signal in the data set, having received anthropogenic Os sporadically since the mid-20th Century. Transport of particles to this site overrode the northward flowing bottom currents. Finding anthropogenic Os at this site cautions that other particle-borne substances, including hazardous ones, could be dispersed broadly in this estuary.
NASA Technical Reports Server (NTRS)
Ginoux, Paul; Prospero, Joseph M.; Gill, Thomas E.; Hsu, N. Christina; Zhao, Ming
2012-01-01
Our understanding of the global dust cycle is limited by a dearth of information about dust sources, especially small-scale features which could account for a large fraction of global emissions. Here we present a global-scale high-resolution (0.1 deg) mapping of sources based on Moderate Resolution Imaging Spectroradiometer (MODIS) Deep Blue estimates of dust optical depth in conjunction with other data sets including land use. We ascribe dust sources to natural and anthropogenic (primarily agricultural) origins, calculate their respective contributions to emissions, and extensively compare these products against literature. Natural dust sources globally account for 75% of emissions; anthropogenic sources account for 25%. North Africa accounts for 55% of global dust emissions with only 8% being anthropogenic, mostly from the Sahel. Elsewhere, anthropogenic dust emissions can be much higher (75% in Australia). Hydrologic dust sources (e.g., ephemeral water bodies) account for 31% worldwide; 15% of them are natural while 85% are anthropogenic. Globally, 20% of emissions are from vegetated surfaces, primarily desert shrublands and agricultural lands. Since anthropogenic dust sources are associated with land use and ephemeral water bodies, both in turn linked to the hydrological cycle, their emissions are affected by climate variability. Such changes in dust emissions can impact climate, air quality, and human health. Improved dust emission estimates will require a better mapping of threshold wind velocities, vegetation dynamics, and surface conditions (soil moisture and land use) especially in the sensitive regions identified here, as well as improved ability to address small-scale convective processes producing dust via cold pool (haboob) events frequent in monsoon regimes.
NASA Astrophysics Data System (ADS)
Wang, Shanshan; Cao, Zhimin; Lan, Dongzhao; Zheng, Zhichang; Li, Guihai
2008-09-01
Grain size parameters, trace metals (Co, Cu, Ni, Pb, Cr, Zn, Ba, Zr and Sr) and total organic matter (TOM) of 38 surficial sediments and a sediment core of west-four Pearl River Estuary region were analyzed. The spacial distribution and the transportation procession of the chemical element in surficial sediments were studied mainly. Multivariate statistics are used to analyses the interrelationship of metal elements, TOM and the grain size parameters. The results demonstrated that terrigenous sediment taken by the rivers are main sources of the trace metal elements and TOM, and the lithology of parent material is a dominating factor controlling the trace metal composition in the surficial sediment. In addition, the hydrodynamic condition and landform are the dominating factors controlling the large-scale distribution, while the anthropogenic input in the coastal area alters the regional distribution of heavy metal elements Co, Cu, Ni, Pb, Cr and Zn. The enrichment factor (EF) analysis was used for the differentiation of the metal source between anthropogenic and naturally occurring, and for the assessment of the anthropogenic influence, the deeper layer content of heavy metals were calculated as the background values and Zr was chosen as the reference element for Co, Cu, Ni, Pb, Cr and Zn. The result indicate prevalent enrichment of Co, Cu, Ni, Pb and Cr, and the contamination of Pb is most obvious, further more, the peculiar high EF value sites of Zn and Pb probably suggest point source input.
NASA Astrophysics Data System (ADS)
Rapp, M.; Ehret, G.; Fix, A.; Wirth, M.; Amediek, A.; Kiemle, C.; Quatrevalet, M.; Butz, A.; Roiger, A.; Joeckel, P.
2017-12-01
For meeting the goals of the Paris agreement it is highly desirable to obtain objective global information on anthropogenic greenhouse gas emission rates. A promising approach for a space based observation system is the combination of active and passive remote sensing from satellites in Low Earth Orbit (LEO). While LIDAR techniques have the potential to yield low bias observations which are independent of solar illumination and hence also work during night and at polar winter latitudes, spectroscopic observations of scattered sunlight are suitable for imaging atmospheric concentrations at high spatial resolution. This presentation reviews progress and plans of work conducted at the German Aerospace Center (DLR). Regarding active remote sensing, DLR has developed the airborne Integrated Path Differential Absorption (IPDA)-Lidar CHARM-F (CO2 and CH4 Remote Monitoring—Flugzeug) for the quantification of carbon dioxide and methane column mixing ratios. CHARM-F has been deployed in an initial airborne field campaign in spring 2015 and results of strong anthropogenic sources detected during these flights will be presented. In addition, DLR is in the process of preparing an international airborne campaign (CoMet - Carbon Dioxide and Methane Mission for HALO) for April 2018 which will be supported by various in-situ, ground based, and modelling activities. These airborne field campaigns are important steps towards the German-French satellite mission MERLIN which also utilizes an IPDA-LIDAR. Also, DLR has started to further investigate concepts for a future space borne IPDA-Lidar for the quantification of strong anthropogenic CO2 point sources. Jointly with the latter, DLR is currently further studying the concept of a passive spectrometer for the observation of CO2 point emissions.
Geochemical evidence for diversity of dust sources in the southwestern United States
Reheis, M.C.; Budahn, J.R.; Lamothe, P.J.
2002-01-01
Several potential dust sources, including generic sources of sparsely vegetated alluvium, playa deposits, and anthropogenic emissions, as well as the area around Owens Lake, California, affect the composition of modern dust in the southwestern United States. A comparison of geochemical analyses of modern and old (a few thousand years) dust with samples of potential local sources suggests that dusts reflect four primary sources: (1) alluvial sediments (represented by Hf, K, Rb, Zr, and rare-earth elements, (2) playas, most of which produce calcareous dust (Sr, associated with Ca), (3) the area of Owens (dry) Lake, a human-induced playa (As, Ba, Li, Pb, Sb, and Sr), and (4) anthropogenic and/or volcanic emissions (As, Cr, Ni, and Sb). A comparison of dust and source samples with previous analyses shows that Owens (dry) Lake and mining wastes from the adjacent Cerro Gordo mining district are the primary sources of As, Ba, Li, and Pb in dusts from Owens Valley. Decreases in dust contents of As, Ba, and Sb with distance from Owens Valley suggest that dust from southern Owens Valley is being transported at least 400 km to the east. Samples of old dust that accumulated before European settlement are distinctly lower in As, Ba, and Sb abundances relative to modern dust, likely due to modern transport of dust from Owens Valley. Thus, southern Owens Valley appears to be an important, geochemically distinct, point source for regional dust in the southwestern United States. Copyright ?? 2002 Elsevier Science Ltd.
Burn-Nunes, Laurie; Vallelonga, Paul; Lee, Khanghyun; Hong, Sungmin; Burton, Graeme; Hou, Shugui; Moy, Andrew; Edwards, Ross; Loss, Robert; Rosman, Kevin
2014-07-15
Lead (Pb) isotopic compositions and concentrations, and barium (Ba) and indium (In) concentrations have been analysed at sub-annual resolution in three sections from a <110 m ice core dated to the 18th and 20th centuries, as well as snow pit samples dated to 2004/2005, recovered from the East Rongbuk Glacier in the high-altitude Himalayas. Ice core sections indicate that atmospheric chemistry prior to ~1,953 was controlled by mineral dust inputs, with no discernible volcanic or anthropogenic contributions. Eighteenth century monsoon ice core chemistry is indicative of dominant contributions from local Himalayan sources; non-monsoon ice core chemistry is linked to contributions from local (Himalayan), regional (Indian/Thar Desert) and long-range (North Africa, Central Asia) sources. Twentieth century monsoon and non-monsoon ice core data demonstrate similar seasonal sources of mineral dust, however with a transition to less-radiogenic isotopic signatures that suggests local and regional climate/environmental change. The snow pit record demonstrates natural and anthropogenic contributions during both seasons, with increased anthropogenic influence during non-monsoon times. Monsoon anthropogenic inputs are most likely sourced to South/South-East Asia and/or India, whereas non-monsoon anthropogenic inputs are most likely sourced to India and Central Asia. Copyright © 2014 Elsevier B.V. All rights reserved.
Anthropogenic combustion iron as a complex climate forcer
Matsui, Hitoshi; Mahowald, Natalie M.; Moteki, Nobuhiro; ...
2018-04-23
Atmospheric iron affects the global carbon cycle by modulating ocean biogeochemistry through the deposition of soluble iron to the ocean. Iron emitted by anthropogenic (fossil fuel) combustion is a source of soluble iron that is currently considered less important than other soluble iron sources, such as mineral dust and biomass burning. Here we show that the atmospheric burden of anthropogenic combustion iron is 8 times greater than previous estimates by incorporating recent measurements of anthropogenic magnetite into a global aerosol model. This new estimation increases the total deposition flux of soluble iron to southern oceans (30–90 °S) by 52%, withmore » a larger contribution of anthropogenic combustion iron than dust and biomass burning sources. The direct radiative forcing of anthropogenic magnetite is estimated to be 0.021 W m –2 globally and 0.22 W m –2 over East Asia. In conclusion, our results demonstrate that anthropogenic combustion iron is a larger and more complex climate forcer than previously thought, and therefore plays a key role in the Earth system.« less
Anthropogenic combustion iron as a complex climate forcer
DOE Office of Scientific and Technical Information (OSTI.GOV)
Matsui, Hitoshi; Mahowald, Natalie M.; Moteki, Nobuhiro
Atmospheric iron affects the global carbon cycle by modulating ocean biogeochemistry through the deposition of soluble iron to the ocean. Iron emitted by anthropogenic (fossil fuel) combustion is a source of soluble iron that is currently considered less important than other soluble iron sources, such as mineral dust and biomass burning. Here we show that the atmospheric burden of anthropogenic combustion iron is 8 times greater than previous estimates by incorporating recent measurements of anthropogenic magnetite into a global aerosol model. This new estimation increases the total deposition flux of soluble iron to southern oceans (30–90 °S) by 52%, withmore » a larger contribution of anthropogenic combustion iron than dust and biomass burning sources. The direct radiative forcing of anthropogenic magnetite is estimated to be 0.021 W m –2 globally and 0.22 W m –2 over East Asia. In conclusion, our results demonstrate that anthropogenic combustion iron is a larger and more complex climate forcer than previously thought, and therefore plays a key role in the Earth system.« less
Terrestrial laser scanning in monitoring of anthropogenic objects
NASA Astrophysics Data System (ADS)
Zaczek-Peplinska, Janina; Kowalska, Maria
2017-12-01
The registered xyz coordinates in the form of a point cloud captured by terrestrial laser scanner and the intensity values (I) assigned to them make it possible to perform geometric and spectral analyses. Comparison of point clouds registered in different time periods requires conversion of the data to a common coordinate system and proper data selection is necessary. Factors like point distribution dependant on the distance between the scanner and the surveyed surface, angle of incidence, tasked scan's density and intensity value have to be taken into consideration. A prerequisite for running a correct analysis of the obtained point clouds registered during periodic measurements using a laser scanner is the ability to determine the quality and accuracy of the analysed data. The article presents a concept of spectral data adjustment based on geometric analysis of a surface as well as examples of geometric analyses integrating geometric and physical data in one cloud of points: cloud point coordinates, recorded intensity values, and thermal images of an object. The experiments described here show multiple possibilities of usage of terrestrial laser scanning data and display the necessity of using multi-aspect and multi-source analyses in anthropogenic object monitoring. The article presents examples of multisource data analyses with regard to Intensity value correction due to the beam's incidence angle. The measurements were performed using a Leica Nova MS50 scanning total station, Z+F Imager 5010 scanner and the integrated Z+F T-Cam thermal camera.
USDA-ARS?s Scientific Manuscript database
Aerosols or airborne dust can originate from sources unrelated to anthropogenic activity but may also be initiated or exacerbated by anthropogenic actions. Anthropogenic dust refers to dust activity (emission and suppression) that is present due to human activity. Wind erosion in the U.S. is a sign...
Carter, Janet M.; Moran, Michael J.; Zogorski, John S.; Price, Curtis V.
2012-01-01
Multiple lines of evidence for indicating factors associated with the sources, transport, and fate of chloroform and three other trihalomethanes (THMs) in untreated groundwater were revealed by evaluating low-level analytical results and logistic regression results for THMs. Samples of untreated groundwater from wells used for drinking water were collected from 1996-2007 from 2492 wells across the United States and analyzed for chloroform, bromodichloromethane, dibromochloromethane, and bromoform by a low-level analytical method implemented in April 1996. Using an assessment level of 0.02 μg/L, chloroform was detected in 36.5% of public-well samples and 17.6% of domestic-well samples, with most concentrations less than 1 μg/L. Brominated THMs occurred less frequently than chloroform but more frequently in public-well samples than domestic-well samples. For both public and domestic wells, THMs occurred most frequently in urban areas. Logistic regression analyses showed that the occurrence of THMs was related to nonpoint sources such as urban land use and to point sources like septic systems. The frequent occurrence and concentration distribution pattern of THMs, as well as their frequent co-occurrence with other organic compounds and nitrate, all known to have anthropogenic sources, and the positive associations between THM occurrence and dissolved oxygen and recharge indicate the recycling of water that contains THMs and other anthropogenic contaminants.
NASA Astrophysics Data System (ADS)
Li, Nan; He, Qingyang; Greenberg, Jim; Guenther, Alex; Li, Jingyi; Cao, Junji; Wang, Jun; Liao, Hong; Wang, Qiyuan; Zhang, Qiang
2018-05-01
This study is the first attempt to understand the synergistic impact of anthropogenic and biogenic emissions on summertime ozone (O3) formation in the Guanzhong (GZ) Basin where Xi'an, the oldest and the most populous city (with a population of 9 million) in northwestern China, is located. Month-long (August 2011) WRF-Chem simulations with different sensitivity experiments were conducted and compared with near-surface measurements. Biogenic volatile organic compounds (VOCs) concentrations was characterized from six surface sites among the Qinling Mountains, and urban air composition was measured in Xi'an city at a tower 100 m a. s. The WRF-Chem control experiment reasonably reproduced the magnitudes and variations of observed O3, VOCs, NOx, PM2.5, and meteorological parameters, with normalized mean biases for each parameter within ±21 %. Subsequent analysis employed the factor separation approach (FSA) to quantitatively disentangle the pure and synergistic impacts of anthropogenic and/or biogenic sources on summertime O3 formation. The impact of anthropogenic sources alone was found to be dominant for O3 formation. Although anthropogenic particles reduced NO2 photolysis by up to 60 %, the anthropogenic sources contributed 19.1 ppb O3 formation on average for urban Xi'an. The abundant biogenic VOCs from the nearby forests promoted O3 formation in urban areas by interacting with the anthropogenic NOx. The calculated synergistic contribution (from both biogenic and anthropogenic sources) was up to 14.4 ppb in urban Xi'an, peaking in the afternoon. Our study reveals that the synergistic impact of individual source contributions to O3 formation should be considered in the formation of air pollution control strategies, especially for big cities in the vicinity of forests.
Influence of Diffused Sourcers of Water Pollution In The Basin of Volga River
NASA Astrophysics Data System (ADS)
Vasilchenco, O.
The intensive development of industry and agriculture, great growth of cities in the last decades result in an increase of the nature water consumption and deterioration. Different anthropogenic load change characteristics of water objects regime and de- pletion and qualitative degradation of water resources. Sources of pollution are divided on two classes: controlled and uncontrolled. The first includes industrial and domestic wastewater disposal. Their discharge and concentration of pollutants are quite stable. These sources of pollution are identified as "point". Surface run-off from of cities, industrial platforms, agricultural object, navigation, recreation are not controlled have dispersed nature and are identification as diffuse. Pollution from such sources is es- timates by computation. Quantitative assumption of pollution amounts reaches water objects is complicated and independent problem. The significant amount of full-scale observations and information processes of concerning dissolved and fluidized frag- ments movement are required. According to available guidelines the part of the pollu- tant entering water objects, is about 1-10For estimation of pollution mass and transport are mathematical modeling. Preliminary calculations of contaminants transport for different territories under an- thropogenic impact of river-Volga basin were made either for point sources of pol- lution or for non-point. Received data made it possible to analyze the correlation of contaminant volumes, coming from different sources pollution.
NASA Astrophysics Data System (ADS)
Turner, A. J.; Jacob, D. J.; Wecht, K. J.; Maasakkers, J. D.; Biraud, S. C.; Boesch, H.; Bowman, K. W.; Deutscher, N. M.; Dubey, M. K.; Griffith, D. W. T.; Hase, F.; Kuze, A.; Notholt, J.; Ohyama, H.; Parker, R.; Payne, V. H.; Sussmann, R.; Velazco, V. A.; Warneke, T.; Wennberg, P. O.; Wunch, D.
2015-02-01
We use 2009-2011 space-borne methane observations from the Greenhouse Gases Observing SATellite (GOSAT) to constrain global and North American inversions of methane emissions with 4° × 5° and up to 50 km × 50 km spatial resolution, respectively. The GOSAT data are first evaluated with atmospheric methane observations from surface networks (NOAA, TCCON) and aircraft (NOAA/DOE, HIPPO), using the GEOS-Chem chemical transport model as a platform to facilitate comparison of GOSAT with in situ data. This identifies a high-latitude bias between the GOSAT data and GEOS-Chem that we correct via quadratic regression. The surface and aircraft data are subsequently used for independent evaluation of the methane source inversions. Our global adjoint-based inversion yields a total methane source of 539 Tg a-1 and points to a large East Asian overestimate in the EDGARv4.2 inventory used as a prior. Results serve as dynamic boundary conditions for an analytical inversion of North American methane emissions using radial basis functions to achieve high resolution of large sources and provide full error characterization. We infer a US anthropogenic methane source of 40.2-42.7 Tg a-1, as compared to 24.9-27.0 Tg a-1 in the EDGAR and EPA bottom-up inventories, and 30.0-44.5 Tg a-1 in recent inverse studies. Our estimate is supported by independent surface and aircraft data and by previous inverse studies for California. We find that the emissions are highest in the South-Central US, the Central Valley of California, and Florida wetlands, large isolated point sources such as the US Four Corners also contribute. We attribute 29-44% of US anthropogenic methane emissions to livestock, 22-31% to oil/gas, 20% to landfills/waste water, and 11-15% to coal with an additional 9.0-10.1 Tg a-1 source from wetlands.
Alberti, Luca; Colombo, Loris; Formentin, Giovanni
2018-04-15
The Lombardy Region in Italy is one of the most urbanized and industrialized areas in Europe. The presence of countless sources of groundwater pollution is therefore a matter of environmental concern. The sources of groundwater contamination can be classified into two different categories: 1) Point Sources (PS), which correspond to areas releasing plumes of high concentrations (i.e. hot-spots) and 2) Multiple-Point Sources (MPS) consisting in a series of unidentifiable small sources clustered within large areas, generating an anthropogenic diffuse contamination. The latter category frequently predominates in European Functional Urban Areas (FUA) and cannot be managed through standard remediation techniques, mainly because detecting the many different source areas releasing small contaminant mass in groundwater is unfeasible. A specific legislative action has been recently enacted at Regional level (DGR IX/3510-2012), in order to identify areas prone to anthropogenic diffuse pollution and their level of contamination. With a view to defining a management plan, it is necessary to find where MPS are most likely positioned. This paper describes a methodology devised to identify the areas with the highest likelihood to host potential MPS. A groundwater flow model was implemented for a pilot area located in the Milan FUA and through the PEST code, a Null-Space Monte Carlo method was applied in order to generate a suite of several hundred hydraulic conductivity field realizations, each maintaining the model in a calibrated state and each consistent with the modelers' expert-knowledge. Thereafter, the MODPATH code was applied to generate back-traced advective flowpaths for each of the models built using the conductivity field realizations. Maps were then created displaying the number of backtracked particles that crossed each model cell in each stochastic calibrated model. The result is considered to be representative of the FUAs areas with the highest likelihood to host MPS responsible for diffuse contamination. Copyright © 2017 Elsevier B.V. All rights reserved.
Morillas, Héctor; Maguregui, Maite; García-Florentino, Cristina; Marcaida, Iker; Madariaga, Juan Manuel
2016-04-15
Dry deposition is one of the most dangerous processes that can take place in the environment where the compounds that are suspended in the atmosphere can react directly on different surrounding materials, promoting decay processes. Usually this process is related with industrial/urban fog and/or marine aerosol in the coastal areas. Particularly, marine aerosol transports different types of salts which can be deposited on building materials and by dry deposition promotes different decay pathways. A new analytical methodology based on the combined use of Raman Spectroscopy and SEM-EDS (point-by-point and imaging) was applied. For that purpose, firstly evaporated seawater (presence of Primary Marine Aerosol (PMA)) was analyzed. After that, using a self-made passive sampler (SMPS), different suspended particles coming from marine aerosol (transformed particles in the atmosphere (Secondary Marine Aerosol (SMA)) and metallic airborne particulate matter coming from anthropogenic sources, were analyzed. Finally in order to observe if SMA and metallic particles identified in the SMPS can be deposited on a building, sandstone samples from La Galea Fortress (Getxo, north of Spain) located in front of the sea and in the place where the passive sampler was mounted were analyzed. Copyright © 2016 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Cereceda-Balic, F.; Palomo-Marín, M. R.; Bernalte, E.; Vidal, V.; Christie, J.; Fadic, X.; Guevara, J. L.; Miro, C.; Pinilla Gil, E.
2012-02-01
Seasonal snow precipitation in the Andes mountain range is evaluated as an environmental indicator of the composition of atmospheric emissions in Santiago de Chile metropolitan area, by measuring a set of representative trace elements in snow samples by ICP-MS. Three late winter sampling campaigns (2003, 2008 and 2009) were conducted in three sampling areas around Cerro Colorado, a Central Andes mountain range sector NE of Santiago (36 km). Nevados de Chillán, a sector in The Andes located about 500 km south from the metropolitan area, was selected as a reference area. The experimental results at Cerro Colorado and Nevados de Chillán were compared with previously published data of fresh snow from remote and urban background sites. High snow concentrations of a range of anthropogenic marker elements were found at Cerro Colorado, probably derived from Santiago urban aerosol transport and deposition combined with the effect of mining and smelting activities in the area, whereas Nevados de Chillán levels roughly correspond to urban background areas. Enhanced concentrations in surface snow respect to deeper samples are discussed. Significant differences found between the 2003, 2008 and 2009 anthropogenic source markers profiles at Cerro Colorado sampling points were correlated with changes in emission sources at the city. The preliminary results obtained in this study, the first of this kind in the southern hemisphere, show promising use of snow precipitation in the Central Andes as a suitable matrix for receptor model studies aimed at identifying and quantifying pollution sources in Santiago de Chile.
Detection of anthropogenic dust using CALIPSO lidar measurements
NASA Astrophysics Data System (ADS)
Huang, J.; Liu, J.; Chen, B.; Nasiri, S. L.
2015-04-01
Anthropogenic dusts are those produced by human activities on disturbed soils, which are mainly cropland, pasture, and urbanized regions and are a subset of the total dust load which includes natural sources from desert regions. Our knowledge of anthropogenic dusts is still very limited due to a lack of data on source distribution and magnitude, and on their effect on radiative forcing which may be comparable to other anthropogenic aerosols. To understand the contribution of anthropogenic dust to the total global dust load and its effect on radiative transfer and climate, it is important to identify them from total dust. In this study, a new technique for distinguishing anthropogenic dust from natural dust is proposed by using Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) dust and planetary boundary layer (PBL) height retrievals along with a land use dataset. Using this technique, the global distribution of dust is analyzed and the relative contribution of anthropogenic and natural dust sources to regional and global emissions are estimated. Results reveal that local anthropogenic dust aerosol due to human activity, such as agriculture, industrial activity, transportation, and overgrazing, accounts for about 25% of the global continental dust load. Of these anthropogenic dust aerosols, more than 53% come from semi-arid and semi-wet regions. Annual mean anthropogenic dust column burden (DCB) values range from 0.42 g m-2 with a maximum in India to 0.12 g m-2 with a minimum in North America. A better understanding of anthropogenic dust emission will enable us to focus on human activities in these critical regions and with such knowledge we will be better able to improve global dust models and to explore the effects of anthropogenic emission on radiative forcing, climate change and air quality in the future.
Huang, Yu; Sun, Jie; Li, Aimin; Xie, Xianchuan
2018-05-01
In this study, an integrated approach named the '333' strategy was applied to pollution control in the Jialu River, in northern China, which is heavily burdened with anthropogenic pollution. Due to a deficiency of the natural ecological inflow, the Jialu River receives predominantly industrial and municipal effluent. The '333' strategy is composed of three steps of pollution control including industrial point-source pollution control, advanced treatment of municipal wastewater, and ecological restoration; three increased stringency emission standards; and three stages of reclamation. Phase 1 of the '333' strategy focuses on industrial point-source pollution control; phase 2 aims to harness municipal wastewater and minimize sewage effluents using novel techniques for advanced water purification; phase 3 of the '333' strategy focuses on the further purification of effluents flowing into Jialu River with the employment of an engineering-based ecological restoration project. The application of the '333' strategy resulted in the development of novel techniques for water purification including modified magnetic resins (NDMP resin), a two-stage internal circulation anaerobic reactor (IC reactor) and an ecological restoration system. The results indicate that water quality in the river was significantly improved, with increased concentrations of dissolved oxygen (DO), as well as reduction of COD by 42.8% and NH 3 -N by 61.4%. In addition, it was observed that the total population of phytoplankton in treated river water notably increased from only one prior to restoration to 8 following restoration. This system also provides a tool for pollution control of other similar industrial and anthropogenic source polluted rivers.
Sampling Singular and Aggregate Point Sources of Carbon Dioxide from Space Using OCO-2
NASA Astrophysics Data System (ADS)
Schwandner, F. M.; Gunson, M. R.; Eldering, A.; Miller, C. E.; Nguyen, H.; Osterman, G. B.; Taylor, T.; O'Dell, C.; Carn, S. A.; Kahn, B. H.; Verhulst, K. R.; Crisp, D.; Pieri, D. C.; Linick, J.; Yuen, K.; Sanchez, R. M.; Ashok, M.
2016-12-01
Anthropogenic carbon dioxide (CO2) sources increasingly tip the natural balance between natural carbon sources and sinks. Space-borne measurements offer opportunities to detect and analyze point source emission signals anywhere on Earth. Singular continuous point source plumes from power plants or volcanoes turbulently mix into their proximal background fields. In contrast, plumes of aggregate point sources such as cities, and transportation or fossil fuel distribution networks, mix into each other and may therefore result in broader and more persistent excess signals of total column averaged CO2 (XCO2). NASA's first satellite dedicated to atmospheric CO2observation, the Orbiting Carbon Observatory-2 (OCO-2), launched in July 2014 and now leads the afternoon constellation of satellites (A-Train). While continuously collecting measurements in eight footprints across a narrow ( < 10 km) wide swath it occasionally cross-cuts coincident emission plumes. For singular point sources like volcanoes and coal fired power plants, we have developed OCO-2 data discovery tools and a proxy detection method for plumes using SO2-sensitive TIR imaging data (ASTER). This approach offers a path toward automating plume detections with subsequent matching and mining of OCO-2 data. We found several distinct singular source CO2signals. For aggregate point sources, we investigated whether OCO-2's multi-sounding swath observing geometry can reveal intra-urban spatial emission structures in the observed variability of XCO2 data. OCO-2 data demonstrate that we can detect localized excess XCO2 signals of 2 to 6 ppm against suburban and rural backgrounds. Compared to single-shot GOSAT soundings which detected urban/rural XCO2differences in megacities (Kort et al., 2012), the OCO-2 swath geometry opens up the path to future capabilities enabling urban characterization of greenhouse gases using hundreds of soundings over a city at each satellite overpass. California Institute of Technology
A tiered observational system for anthropogenic methane emissions
NASA Astrophysics Data System (ADS)
Duren, R. M.; Miller, C. E.; Hulley, G. C.; Hook, S. J.; Sander, S. P.
2014-12-01
Improved understanding of anthropogenic methane emissions is required for closing the global carbon budget and addressing priority challenges in climate policy. Several decades of top-down and bottom-up studies show that anthropogenic methane emissions are systematically underestimated in key regions and economic sectors. These uncertainties have been compounded by the dramatic rise of disruptive technologies (e.g., the transformation in the US energy system due to unconventional gas and oil production). Methane flux estimates derived from inverse analyses and aircraft-based mass balance approaches underscore the disagreement in nationally and regionally reported methane emissions as well as the possibility of a long-tail distribution in fugitive emissions spanning the US natural gas supply chain; i.e. a small number of super-emitters may be responsible for most of the observed anomalies. Other studies highlight the challenges of sectoral and spatial attribution of fugitive emissions - including the relative contributions of dairies vs oil and gas production or disentangling the contributions of natural gas transmission, distribution, and consumption or landfill emissions in complex urban environments. Limited observational data remains a foundational barrier to resolving these challenges. We present a tiered observing system strategy for persistent, high-frequency monitoring over large areas to provide remote detection, geolocation and quantification of significant anthropogenic methane emissions across cities, states, basins and continents. We describe how this would both improve confidence in methane emission estimates and expedite resolution of fugitive emissions and leaks. We summarize recent prototype field campaigns that employ multiple vantage points and measurement techniques (including NASA's CARVE and HyTES aircraft and PanFTS instrument on Mt Wilson). We share preliminary results of this tiered observational approach including examples of individual methane point sources associated with oil and gas production and distribution, feedlots, and urban landfills in California.
Most global methane (CH4) budgets have failed to include emissions from a diverse group of minor anthropogenic sources. Individually, these minor sources emit small quantities of CH4, but collectively, their contributions to the budget may be significant. In this paper, CH4 emiss...
Deconstructing Demand: The Anthropogenic and Climatic Drivers of Urban Water Consumption.
Hemati, Azadeh; Rippy, Megan A; Grant, Stanley B; Davis, Kristen; Feldman, David
2016-12-06
Cities in drought prone regions of the world such as South East Australia are faced with escalating water scarcity and security challenges. Here we use 72 years of urban water consumption data from Melbourne, Australia, a city that recently overcame a 12 year "Millennium Drought", to evaluate (1) the relative importance of climatic and anthropogenic drivers of urban water demand (using wavelet-based approaches) and (2) the relative contribution of various water saving strategies to demand reduction during the Millennium Drought. Our analysis points to conservation as a dominant driver of urban water savings (69%), followed by nonrevenue water reduction (e.g., reduced meter error and leaks in the potable distribution system; 29%), and potable substitution with alternative sources like rain or recycled water (3%). Per-capita consumption exhibited both climatic and anthropogenic signatures, with rainfall and temperature explaining approximately 55% of the variance. Anthropogenic controls were also strong (up to 45% variance explained). These controls were nonstationary and frequency-specific, with conservation measures like outdoor water restrictions impacting seasonal water use and technological innovation/changing social norms impacting lower frequency (baseline) use. The above-noted nonstationarity implies that wavelets, which do not assume stationarity, show promise for use in future predictive models of demand.
NASA Astrophysics Data System (ADS)
Mekonnen, Mesfin M.; Hoekstra, Arjen Y.
2018-01-01
We estimate the global anthropogenic phosphorus (P) loads to freshwater and the associated grey water footprints (GWFs) for the period 2002-2010, at a spatial resolution of 5 × 5 arc min, and compare the GWF per river basin to runoff to assess the P-related water pollution level (WPL). The global anthropogenic P load to freshwater systems from both diffuse and point sources is estimated at 1.5 Tg/yr. More than half of this total load was in Asia, followed by Europe (19%) and Latin America and the Caribbean (13%). The domestic sector contributed 54% to the total, agriculture 38%, and industry 8%. In agriculture, cereals production had the largest contribution to the P load (31%), followed by fruits, vegetables, and oil crops, each contributing 15%. The global total GWF related to anthropogenic P loads is estimated to be 147 × 1012 m3/yr, with China contributing 30%, India 8%, USA 7%, and Spain and Brazil 6% each. The basins with WPL > 1 (where GWF exceeds the basin's assimilation capacity) together cover about 38% of the global land area, 37% of the global river discharge, and provide residence to about 90% of the global population.
Aerosol composition and its sources at the King Sejong Station, Antarctic peninsula
NASA Astrophysics Data System (ADS)
Mishra, Vinit K.; Kim, Ki-Hyun; Hong, Sungmin; Lee, Khanghyun
The annual cycles of major metals and ions in suspended particulate matters (SPM) have been investigated at a costal site of the Antarctic Peninsula in order to elucidate temporal variations as well as major source processes responsible for their formation. The measurements had been performed from January 2000 to December 2001 at the Korean Antarctic research station, 'King Sejong' (62°13' S, 58°47' W). The observed time series of important aerosol components showed clear seasonal variation patterns, while the mean elemental concentrations (e.g., 1875 (Al), 10.3 (Ba), 0.3 (Bi), 1.3 (Cd), 1.7 pg m -3 (Co)) were generally compatible with those reported previously. The presence of high EF values with respect to both mean crustal and seawater composition (such as Bi, Cd, Cr, Cu, Ni, V, and Zn), however, suggests a possibly important role of anthropogenic processes in this remote site. In contrast, the concentrations of ionic species were not clearly distinguishable from those of other Antarctic sites; but the consideration of ionic mass balance between cations and anions pointed out the uniqueness of their source/sink processes in the study area. The major source processes of those aerosol components were also investigated using a series of statistical analyses. The overall results of our study indicated the dominance of several processes (or sources) such as sea-salt emission, secondary aerosol formation, and anthropogenic pollution from both local and distant sources.
Anthropogenic tracers, endocrine disrupting chemicals, and endocrine disruption in Minnesota lakes
Writer, J.H.; Barber, L.B.; Brown, G.K.; Taylor, Howard E.; Kiesling, R.L.; Ferrey, M.L.; Jahns, N.D.; Bartell, S.E.; Schoenfuss, H.L.
2010-01-01
Concentrations of endocrine disrupting chemicals and endocrine disruption in fish were determined in 11 lakes across Minnesota that represent a range of trophic conditions and land uses (urban, agricultural, residential, and forested) and in which wastewater treatment plant discharges were absent. Water, sediment, and passive polar organic integrative samplers (POCIS) were analyzed for steroidal hormones, alkylphenols, bisphenol A, and other organic and inorganic molecular tracers to evaluate potential non-point source inputs into the lakes. Resident fish from the lakes were collected, and caged male fathead minnows were deployed to evaluate endocrine disruption, as indicated by the biological endpoints of plasma vitellogenin and gonadal histology. Endocrine disrupting chemicals, including bisphenol A, 17??-estradiol, estrone, and 4-nonylphenol were detected in 90% of the lakes at part per trillion concentrations. Endocrine disruption was observed in caged fathead minnows and resident fish in 90% of the lakes. The widespread but variable occurrence of anthropogenic chemicals in the lakes and endocrine disruption in fish indicates that potential sources are diverse, not limited to wastewater treatment plant discharges, and not entirely predictable based on trophic status and land use. ?? 2010.
Climate response of the South Asian monsoon system to anthropogenic aerosols
DOE Office of Scientific and Technical Information (OSTI.GOV)
Ganguly, Dilip; Rasch, Philip J.; Wang, Hailong
2012-07-13
The equilibrium climate response to the total effects (direct, indirect and semi-direct effects) of aerosols arising from anthropogenic and biomass burning emissions on the South Asian summer monsoon system is studied using a coupled atmosphere-slab ocean model. Our results suggest that anthropogenic and biomass burning aerosols generally induce a reduction in mean summer monsoon precipitation over most parts of the Indian subcontinent, strongest along the western coastline of the Indian peninsula and eastern Nepal region, but modest increases also occur over the north western part of the subcontinent. While most of the noted reduction in precipitation is triggered by increasedmore » emissions of aerosols from anthropogenic activities, modest increases in the north west are mostly associated with decreases in local emissions of aerosols from forest fire and grass fire sources. Anthropogenic aerosols from outside Asia also contribute to the overall reduction in precipitation but the dominant contribution comes from aerosol sources within Asia. Local emissions play a more important role in the total rainfall response to anthropogenic aerosol sources during the early monsoon period, whereas both local as well as remote emissions of aerosols play almost equally important roles during the later part of the monsoon period. While precipitation responses are primarily driven by local aerosol forcing, regional surface temperature changes over the region are strongly influenced by anthropogenic aerosols from sources further away (non-local changes). Changes in local anthropogenic organic and black carbon emissions by as much as a factor of two (preserving their ratio) produce the same basic signatures in the model's summer monsoon temperature and precipitation responses.« less
Monoterpenes are the largest source of summertime organic aerosol in the southeastern United States
Zhang, Haofei; Yee, Lindsay D.; Lee, Ben H.; ...
2018-02-12
The chemical complexity of atmospheric organic aerosol (OA) has caused substantial uncertainties in understanding its origins and environmental impacts. Here, we provide constraints on OA origins through compositional characterization with molecular-level details. Our results suggest that secondary OA (SOA) from monoterpene oxidation accounts for approximately half of summertime fine OA in Centreville, AL, a forested area in the southeastern United States influenced by anthropogenic pollution. We find that different chemical processes involving nitrogen oxides, during days and nights, play a central role in determining the mass of monoterpene SOA produced. These findings elucidate the strong anthropogenic–biogenic interaction affecting ambient aerosolmore » in the southeastern United States and point out the importance of reducing anthropogenic emissions, especially under a changing climate, where biogenic emissions will likely keep increasing.« less
Monoterpenes are the largest source of summertime organic aerosol in the southeastern United States
DOE Office of Scientific and Technical Information (OSTI.GOV)
Zhang, Haofei; Yee, Lindsay D.; Lee, Ben H.
The chemical complexity of atmospheric organic aerosol (OA) has caused substantial uncertainties in understanding its origins and environmental impacts. Here, we provide constraints on OA origins through compositional characterization with molecular-level details. Our results suggest that secondary OA (SOA) from monoterpene oxidation accounts for approximately half of summertime fine OA in Centreville, AL, a forested area in the southeastern United States influenced by anthropogenic pollution. We find that different chemical processes involving nitrogen oxides, during days and nights, play a central role in determining the mass of monoterpene SOA produced. These findings elucidate the strong anthropogenic–biogenic interaction affecting ambient aerosolmore » in the southeastern United States and point out the importance of reducing anthropogenic emissions, especially under a changing climate, where biogenic emissions will likely keep increasing.« less
Liu, Mei-bing; Chen, Xing-wei; Chen, Ying
2015-07-01
Identification of the critical source areas of non-point source pollution is an important means to control the non-point source pollution within the watershed. In order to further reveal the impact of multiple time scales on the spatial differentiation characteristics of non-point source nitrogen loss, a SWAT model of Shanmei Reservoir watershed was developed. Based on the simulation of total nitrogen (TN) loss intensity of all 38 subbasins, spatial distribution characteristics of nitrogen loss and critical source areas were analyzed at three time scales of yearly average, monthly average and rainstorms flood process, respectively. Furthermore, multiple linear correlation analysis was conducted to analyze the contribution of natural environment and anthropogenic disturbance on nitrogen loss. The results showed that there were significant spatial differences of TN loss in Shanmei Reservoir watershed at different time scales, and the spatial differentiation degree of nitrogen loss was in the order of monthly average > yearly average > rainstorms flood process. TN loss load mainly came from upland Taoxi subbasin, which was identified as the critical source area. At different time scales, land use types (such as farmland and forest) were always the dominant factor affecting the spatial distribution of nitrogen loss, while the effect of precipitation and runoff on the nitrogen loss was only taken in no fertilization month and several processes of storm flood at no fertilization date. This was mainly due to the significant spatial variation of land use and fertilization, as well as the low spatial variability of precipitation and runoff.
Dust Storm over the Middle East: Retrieval Approach, Source Identification, and Trend Analysis
NASA Astrophysics Data System (ADS)
Moridnejad, A.; Karimi, N.; Ariya, P. A.
2014-12-01
The Middle East region has been considered to be responsible for approximately 25% of the Earth's global emissions of dust particles. By developing Middle East Dust Index (MEDI) and applying to 70 dust storms characterized on MODIS images and occurred during the period between 2001 and 2012, we herein present a new high resolution mapping of major atmospheric dust source points participating in this region. To assist environmental managers and decision maker in taking proper and prioritized measures, we then categorize identified sources in terms of intensity based on extracted indices for Deep Blue algorithm and also utilize frequency of occurrence approach to find the sensitive sources. In next step, by implementing the spectral mixture analysis on the Landsat TM images (1984 and 2012), a novel desertification map will be presented. The aim is to understand how human perturbations and land-use change have influenced the dust storm points in the region. Preliminary results of this study indicate for the first time that c.a., 39 % of all detected source points are located in this newly anthropogenically desertified area. A large number of low frequency sources are located within or close to the newly desertified areas. These severely desertified regions require immediate concern at a global scale. During next 6 months, further research will be performed to confirm these preliminary results.
Zhu, Yanhong; Yang, Lingxiao; Kawamura, Kimitaka; Chen, Jianmin; Ono, Kaori; Wang, Xinfeng; Xue, Likun; Wang, Wenxing
2017-01-01
Ambient fine particulate matter (PM 2.5 ) and volatile organic compounds (VOCs) collected at Mt. Tai in summer 2014 were analysed and the data were used to identify the contribution of biogenic and anthropogenic hydrocarbons to secondary organic aerosols (SOA) and their sources and potential source areas in high mountain regions. Compared with those in 2006, the 2014 anthropogenic SOA tracers in PM 2.5 aerosols and VOC species related to vehicular emissions exhibited higher concentrations, whereas the levels of biogenic SOA tracers were lower, possibly due to decreased biomass burning. Using the SOA tracer and parameterisation method, we estimated the contributions from biogenic and anthropogenic VOCs, respectively. The results showed that the average concentration of biogenic SOA was 1.08 ± 0.51 μg m -3 , among which isoprene SOA tracers were dominant. The anthropogenic VOC-derived SOA were 7.03 ± 1.21 μg m -3 and 1.92 ± 1.34 μg m -3 under low- and high-NO x conditions, respectively, and aromatics made the greatest contribution. However, the sum of biogenic and anthropogenic SOA only contributed 18.1-49.1% of the total SOA. Source apportionment by positive matrix factorisation (PMF) revealed that secondary oxidation and biomass burning were the major sources of biogenic SOA tracers. Anthropogenic aromatics mainly came from solvent use, fuel and plastics combustion and vehicular emissions. However, for > C6 alkanes and cycloalkanes, vehicular emissions and fuel and plastics combustion were the most important contributors. The potential source contribution function (PSCF) identified the Bohai Sea Region (BSR) as the major source area for organic aerosol compounds and VOC species at Mt. Tai. Copyright © 2016 Elsevier Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Philip, Sajeev; Martin, Randall V.; Snider, Graydon; Weagle, Crystal L.; van Donkelaar, Aaron; Brauer, Michael; Henze, Daven K.; Klimont, Zbigniew; Venkataraman, Chandra; Guttikunda, Sarath K.; Zhang, Qiang
2017-04-01
Global measurements of the elemental composition of fine particulate matter across several urban locations by the Surface Particulate Matter Network reveal an enhanced fraction of anthropogenic dust compared to natural dust sources, especially over Asia. We develop a global simulation of anthropogenic fugitive, combustion, and industrial dust which, to our knowledge, is partially missing or strongly underrepresented in global models. We estimate 2-16 μg m-3 increase in fine particulate mass concentration across East and South Asia by including anthropogenic fugitive, combustion, and industrial dust emissions. A simulation including anthropogenic fugitive, combustion, and industrial dust emissions increases the correlation from 0.06 to 0.66 of simulated fine dust in comparison with Surface Particulate Matter Network measurements at 13 globally dispersed locations, and reduces the low bias by 10% in total fine particulate mass in comparison with global in situ observations. Global population-weighted PM2.5 increases by 2.9 μg m-3 (10%). Our assessment ascertains the urgent need of including this underrepresented fine anthropogenic dust source into global bottom-up emission inventories and global models.
EVALUATION OF SIGNIFICANT ANTHROPOGENIC SOURCES OF RADIATIVELY IMPORTANT TRACE GASES
The report is an initial evaluation of significant anthropogenic sources of radiatively important trace gases. missions of greenhouse gases from human activities--including fossil fuel combustion, industrial/agricultural activities, and transportation--contribute to the increasin...
CO source contribution analysis for California during ARCTAS-CARB
NASA Astrophysics Data System (ADS)
Pfister, G. G.; Avise, J.; Wiedinmyer, C.; Edwards, D. P.; Emmons, L. K.; Diskin, G. D.; Podolske, J.; Wisthaler, A.
2011-08-01
Air pollution is of concern in many parts of California and is impacted by both local emissions and also by pollution inflow from the North Pacific Ocean. In this study, we use the regional chemical transport model WRF-Chem V3.2 together with the global Model for OZone and Related Chemical Tracers to examine the CO budget over California. We include model CO tracers for different emission sources in the models, which allow estimation of the relative importance of local sources versus pollution inflow on the distribution of CO at the surface and in the free troposphere. The focus of our study is on the 15 June-15 July 2008 time period, which coincides with the aircraft deployment of the NASA Arctic Research of the Composition of the Troposphere from Aircraft and Satellites (ARCTAS) mission over California. Model simulations are evaluated using these aircraft observations as well as satellite retrievals and surface observations of CO. Evaluation results show that the model overall predicts the observed CO fields well, but points towards an underestimate of CO from the fires in Northern California, which had a strong influence during the study period, and towards a slight overestimate of CO from pollution inflow and local anthropogenic sources. The analysis of the CO budget over California reveals that inflow of CO explains on average 99 ± 11 ppbV of surface CO during the study period, compared to 61 ± 95 ppbV for local anthropogenic direct emissions of CO and 84 ± 194 ppbV for fires. In the free troposphere, the average CO contributions are estimated as 96 ± 7 ppbV for CO inflow, 8 ± 9 ppbV for CO from local anthropogenic sources and 18 ± 13 ppbV for CO from fires. Accounting for the low bias in the CO fire emission inventory, the fire impact during the study period might have been up to a factor 4 higher than the given estimates.
Gridded anthropogenic emissions inventory and atmospheric transport of carbonyl sulfide in the U.S.
NASA Astrophysics Data System (ADS)
Zumkehr, Andrew; Hilton, Timothy W.; Whelan, Mary; Smith, Steve; Campbell, J. Elliott
2017-02-01
Carbonyl sulfide (COS or OCS), the most abundant sulfur-containing gas in the troposphere, has recently emerged as a potentially important atmospheric tracer for the carbon cycle. Atmospheric inverse modeling studies may be able to use existing tower, airborne, and satellite observations of COS to infer information about photosynthesis. However, such analysis relies on gridded anthropogenic COS source estimates that are largely based on industry activity data from over three decades ago. Here we use updated emission factor data and industry activity data to develop a gridded inventory with a 0.1° resolution for the U.S. domain. The inventory includes the primary anthropogenic COS sources including direct emissions from the coal and aluminum industries as well as indirect sources from industrial carbon disulfide emissions. Compared to the previously published inventory, we found that the total anthropogenic source (direct and indirect) is 47% smaller. Using this new gridded inventory to drive the Sulfur Transport and Deposition Model/Weather Research and Forecasting atmospheric transport model, we found that the anthropogenic contribution to COS variation in the troposphere is small relative to the biosphere influence, which is encouraging for carbon cycle applications in this region. Additional anthropogenic sectors with highly uncertain emission factors require further field measurements.
Sources of springtime surface black carbon in the Arctic: an adjoint analysis for April 2008
NASA Astrophysics Data System (ADS)
Qi, Ling; Li, Qinbin; Henze, Daven K.; Tseng, Hsien-Liang; He, Cenlin
2017-08-01
We quantify source contributions to springtime (April 2008) surface black carbon (BC) in the Arctic by interpreting surface observations of BC at five receptor sites (Denali, Barrow, Alert, Zeppelin, and Summit) using a global chemical transport model (GEOS-Chem) and its adjoint. Contributions to BC at Barrow, Alert, and Zeppelin are dominated by Asian anthropogenic sources (40-43 %) before 18 April and by Siberian open biomass burning emissions (29-41 %) afterward. In contrast, Summit, a mostly free tropospheric site, has predominantly an Asian anthropogenic source contribution (24-68 %, with an average of 45 %). We compute the adjoint sensitivity of BC concentrations at the five sites during a pollution episode (20-25 April) to global emissions from 1 March to 25 April. The associated contributions are the combined results of these sensitivities and BC emissions. Local and regional anthropogenic sources in Alaska are the largest anthropogenic sources of BC at Denali (63 % of total anthropogenic contributions), and natural gas flaring emissions in the western extreme north of Russia (WENR) are the largest anthropogenic sources of BC at Zeppelin (26 %) and Alert (13 %). We find that long-range transport of emissions from Beijing-Tianjin-Hebei (also known as Jing-Jin-Ji), the biggest urbanized region in northern China, contribute significantly (˜ 10 %) to surface BC across the Arctic. On average, it takes ˜ 12 days for Asian anthropogenic emissions and Siberian biomass burning emissions to reach the Arctic lower troposphere, supporting earlier studies. Natural gas flaring emissions from the WENR reach Zeppelin in about a week. We find that episodic transport events dominate BC at Denali (87 %), a site outside the Arctic front, which is a strong transport barrier. The relative contribution of these events to surface BC within the polar dome is much smaller (˜ 50 % at Barrow and Zeppelin and ˜ 10 % at Alert). The large contributions from Asian anthropogenic sources are predominately in the form of chronic
pollution (˜ 40 % at Barrow, 65 % at Alert, and 57 % at Zeppelin) on about a 1-month timescale. As such, it is likely that previous studies using 5- or 10-day trajectory analyses strongly underestimated the contribution from Asia to surface BC in the Arctic.
Anthropogenic lead inputs to the western Pacific during the 20th century.
Inoue, Mayuri; Tanimizu, Masaharu
2008-11-15
Unlike in the North Atlantic, no continuous record of anthropogenic lead (Pb) has been available in the western Pacific. We reconstructed historical changes in anthropogenic Pb on the basis of Pb isotope ratios recorded in annually-banded coral retrieved from Ogasawara Island, Japan. Whereas the predominant natural source of Pb to the surface of the western Pacific apparently is Chinese loess, anthropogenic Pb has affected the western Pacific at least since the late 19th century. From the late 19th to the early 20th century, Australian Pb used in Japan was an important source of anthropogenic Pb. During 1920-1940, Pb emitted from parts of the world other than Japan contributed somewhat to the western Pacific, and the amount of Pb imported from Australia declined. Alkyl Pb used in Japan became the main source from 1950 until the mid-1970s, when leaded gasoline began to be regulated in Japan. Since the mid-1980s, aerosols from China have been the predominant source of Pb in the western Pacific. During the 1990s, around 60% of Pb in the surface of the western Pacific was from Chinese aerosols. We also investigated the present spatial distribution and likely sources of Pb in the western Pacific by using coral samples. Enrichment in 208Pb, which is a characteristic of Pb from China, was found in all coral samples except that from Pohnpei, Micronesia, suggesting that at present anthropogenic Pb is transported to the western Pacific mainly from China via westerly winds.
Modeling Nitrogen Processing in Northeast US River Networks
NASA Astrophysics Data System (ADS)
Whittinghill, K. A.; Stewart, R.; Mineau, M.; Wollheim, W. M.; Lammers, R. B.
2013-12-01
Due to increased nitrogen (N) pollution from anthropogenic sources, the need for aquatic ecosystem services such as N removal has also increased. River networks provide a buffering mechanism that retains or removes anthropogenic N inputs. However, the effectiveness of N removal in rivers may decline with increased loading and, consequently, excess N is eventually delivered to estuaries. We used a spatially distributed river network N removal model developed within the Framework for Aquatic Modeling in the Earth System (FrAMES) to examine the geography of N removal capacity of Northeast river systems under various land use and climate conditions. FrAMES accounts for accumulation and routing of runoff, water temperatures, and serial biogeochemical processing using reactivity derived from the Lotic Intersite Nitrogen Experiment (LINX2). Nonpoint N loading is driven by empirical relationships with land cover developed from previous research in Northeast watersheds. Point source N loading from wastewater treatment plants is estimated as a function of the population served and the volume of water discharged. We tested model results using historical USGS discharge data and N data from historical grab samples and recently initiated continuous measurements from in-situ aquatic sensors. Model results for major Northeast watersheds illustrate hot spots of ecosystem service activity (i.e. N removal) using high-resolution maps and basin profiles. As expected, N loading increases with increasing suburban or agricultural land use area. Network scale N removal is highest during summer and autumn when discharge is low and river temperatures are high. N removal as the % of N loading increases with catchment size and decreases with increasing N loading, suburban land use, or agricultural land use. Catchments experiencing the highest network scale N removal generally have N inputs (both point and non-point sources) located in lower order streams. Model results can be used to better predict nutrient loading to the coastal ocean across a broad range of current and future climate variability.
NASA Astrophysics Data System (ADS)
Brannon, E.; Moseman-Valtierra, S.; Quinn, R. K.; Amador, J.; Brown, R.; Lancellotti, B.; Glennon, K.; Celeste, G.; Craver, V.
2016-12-01
Narragansett Bay in Rhode Island is characterized by a substantial, historic bay-wide nitrogen (N) gradient. Centralized wastewater treatment plants (WWTPs) are a major anthropogenic N source. Onsite wastewater treatments systems (OWTS), which serve 1/3 of all households in the state, are another anthropogenic N source. Recent state regulation has prompted upgrades to both WWTPs and OWTS to increase N removal capacities. Although this should lower N loads to Narragansett Bay, it has the potential to increase the flux of nitrous oxide (N2O), a potent greenhouse gas. We measured summer-time (2016) N2O fluxes of a major WWTP (biological N removal system at Field's Point in Providence) and three of the most common advanced OWTS in the Narragansett Bay watershed (Orenco Advantex AX20, BioMicrobics FAST, SeptiTech D Series). We also tested impacts of application of recovered N (biosolids from wastewater sludge) on N2O fluxes from a turfgrass (Schedonerus arundinaceus) and dominant native coastal cordgrass (Spartina alterniflora) in mesocosm experiments. Preliminary results indicate that the largest N2O fluxes (245 ± 72 µmol N2O m-2 h-1) were from the Field's Point WWTP. Significant, but smaller N2O fluxes (6 ± 3 µmol N2O m-2 h-1 were also measured from the OWTS. In contrast, N2O fluxes from the N-enriched native coastal cordgrass and turfgrass mesocosms were often non-detectable. However, fluxes from a few mesocosms (max. of 25 µmol N2O m-2 h-1) were on the same order of magnitude as fluxes from the OWTS. A state-wide budget of N2O emissions from turfgrasses, intertidal marshes, and OWTS will be estimated to determine their significance as sources relative to the Field's Point WWTP. This data will be used to identify areas where N2O fluxes can be minimized in the state of RI.
Wang, Jie; Liu, Guijian; Liu, Houqi; Lam, Paul K S
2017-04-01
A total of 211 water samples were collected from 53 key sampling points from 5-10th July 2013 at four different depths (0m, 2m, 4m, 8m) and at different sites in the Huaihe River, Anhui, China. These points monitored for 18 parameters (water temperature, pH, TN, TP, TOC, Cu, Pb, Zn, Ni, Co, Cr, Cd, Mn, B, Fe, Al, Mg, and Ba). The spatial variability, contamination sources and health risk of trace elements as well as the river water quality were investigated. Our results were compared with national (CSEPA) and international (WHO, USEPA) drinking water guidelines, revealing that Zn, Cd and Pb were the dominant pollutants in the water body. Application of different multivariate statistical approaches, including correlation matrix and factor/principal component analysis (FA/PCA), to assess the origins of the elements in the Huaihe River, identified three source types that accounted for 79.31% of the total variance. Anthropogenic activities were considered to contribute much of the Zn, Cd, Pb, Ni, Co, and Mn via industrial waste, coal combustion, and vehicle exhaust; Ba, B, Cr and Cu were controlled by mixed anthropogenic and natural sources, and Mg, Fe and Al had natural origins from weathered rocks and crustal materials. Cluster analysis (CA) was used to classify the 53 sample points into three groups of water pollution, high pollution, moderate pollution, and low pollution, reflecting influences from tributaries, power plants and vehicle exhaust, and agricultural activities, respectively. The results of the water quality index (WQI) indicate that water in the Huaihe River is heavily polluted by trace elements, so approximately 96% of the water in the Huaihe River is unsuitable for drinking. A health risk assessment using the hazard quotient and index (HQ/HI) recommended by the USEPA suggests that Co, Cd and Pb in the river could cause non-carcinogenic harm to human health. Copyright © 2017 Elsevier B.V. All rights reserved.
Inventories and scenarios of nitrous oxide emissions
NASA Astrophysics Data System (ADS)
Davidson, Eric A.; Kanter, David
2014-10-01
Effective mitigation for N2O emissions, now the third most important anthropogenic greenhouse gas and the largest remaining anthropogenic source of stratospheric ozone depleting substances, requires understanding of the sources and how they may increase this century. Here we update estimates and their uncertainties for current anthropogenic and natural N2O emissions and for emissions scenarios to 2050. Although major uncertainties remain, ‘bottom-up’ inventories and ‘top-down’ atmospheric modeling yield estimates that are in broad agreement. Global natural N2O emissions are most likely between 10 and 12 Tg N2O-N yr-1. Net anthropogenic N2O emissions are now about 5.3 Tg N2O-N yr-1. Gross anthropogenic emissions by sector are 66% from agriculture, 15% from energy and transport sectors, 11% from biomass burning, and 8% from other sources. A decrease in natural emissions from tropical soils due to deforestation reduces gross anthropogenic emissions by about 14%. Business-as-usual emission scenarios project almost a doubling of anthropogenic N2O emissions by 2050. In contrast, concerted mitigation scenarios project an average decline of 22% relative to 2005, which would lead to a near stabilization of atmospheric concentration of N2O at about 350 ppb. The impact of growing demand for biofuels on future projections of N2O emissions is highly uncertain; N2O emissions from second and third generation biofuels could remain trivial or could become the most significant source to date. It will not be possible to completely eliminate anthropogenic N2O emissions from agriculture, but better matching of crop N needs and N supply offers significant opportunities for emission reductions.
NASA Astrophysics Data System (ADS)
Ma, L.; Herndon, E.; Jin, L.; Sanchez, D.; Brantley, S. L.
2013-12-01
Anthropogenic forcings have dominated metal cycling in many environments. During the period of the industrial revolution, mining and smelting of ores and combustion of fossil fuels released non-negligible amounts of potentially toxic metals such as Pb, Cd, Mn, and Zn into the environment. The extent and fate of these metal depositions in soils during that period however, have not been adequately evaluated. Here, we combine Pb isotopes with Cd isotopes to trace the sources of metal pollutants in a small temperate watershed (Shale Hills) in Pennsylvania. Previous work has shown that Mn additions to soils in central PA was caused by early iron production, as well as coal burning and steel making upwind. Comparison of the Pb and Cd concentrations in the bedrock and soils from this watershed show that Pb and Cd in soils at Shale Hills are best characterized by addition profiles, consistent with atmospheric additions. Three soil profiles at Shale Hills on the same hillslope have very similar anthropogenic Pb inventories. Pb isotope results further reveal that the extensive use of local coals during iron production in early 19th century in Pennsylvania is most likely the anthropogenic Pb source for the surface soils at Shale Hills. Pb concentrations and isotope ratios were used to calculate mass balance and diffusive transport models in soil profiles. The model results further reveal that during the 1850s to 1920s, coal burning in local iron blasting furnaces significantly increased the Pb deposition rates to 8-14 μg cm-2 yr-1, even more than modern Pb deposition rates derived from the use of leaded gasoline in the 1940s to 1980s. Furthermore, Cd has a low boiling point (~760 °C) and easily evaporates and condenses. The evaporation and condensation processes could generate systematic mass-dependent isotope fractionation between Cd in coal burning products and the naturally occurring Cd in the sulfide minerals of coals. This fractionation indicates that Cd isotopes can be used as a novel tracer of materials that have been affected by industrial high temperature processes, distinguishing them from natural Cd sources. Our ongoing Cd isotope measurements in the same soil profiles thus hold significant promise for tracing anthropogenic sources of this highly toxic metal in the environment. This will be the first time that Cd isotopes are characterized for polluted soils related to coal-burning activities. Such information will provide the first Cd isotope dataset to assess the environmental impacts due to the use of coals on a global scale. These new Pb and Cd isotope results, along with previous observations of Mn enrichment at Shale Hills, suggest that historical point sources from the industrial revolution could contribute significant amounts of metal contamination to top-soils. Our study highlights the importance of using multiple isotope systems to investigate Critical Zone processes in identical lithology and environmental settings.
Global gridded anthropogenic emissions inventory of carbonyl sulfide
DOE Office of Scientific and Technical Information (OSTI.GOV)
Zumkehr, Andrew; Hilton, Tim; Whelan, Mary
Atmospheric carbonyl sulfide (COS or OCS) is the most abundant sulfur containing gas in the troposphere and is an atmospheric tracer for the carbon cycle. Gridded inventories of global anthropogenic COS are used for interpreting global COS measurements. However, previous gridded anthropogenic data are a climatological estimate based on input data that is over three decades old and are not representative of current conditions. Here we develop a new gridded data set of global anthropogenic COS sources that includes more source sectors than previously available and uses the most current emissions factors and industry activity data as input. Additionally, themore » inventory is provided as annually varying estimates from years 1980–2012 and employs a source specific spatial scaling procedure. We estimate a global source in year 2012 of 406 Gg S y -1 (range of 223–586 Gg S y -1), which is highly concentrated in China and is twice as large as the previous gridded inventory. Our large upward revision in the bottom-up estimate of the source is consistent with a recent top-down estimate based on air-monitoring and Antarctic firn data. Furthermore, our inventory time trends, including a decline in the 1990's and growth after the year 2000, are qualitatively consistent with trends in atmospheric data. Lastly, similarities between the spatial distribution in this inventory and remote sensing data suggest that the anthropogenic source could potentially play a role in explaining a missing source in the global COS budget.« less
Global gridded anthropogenic emissions inventory of carbonyl sulfide
Zumkehr, Andrew; Hilton, Tim; Whelan, Mary; ...
2018-03-31
Atmospheric carbonyl sulfide (COS or OCS) is the most abundant sulfur containing gas in the troposphere and is an atmospheric tracer for the carbon cycle. Gridded inventories of global anthropogenic COS are used for interpreting global COS measurements. However, previous gridded anthropogenic data are a climatological estimate based on input data that is over three decades old and are not representative of current conditions. Here we develop a new gridded data set of global anthropogenic COS sources that includes more source sectors than previously available and uses the most current emissions factors and industry activity data as input. Additionally, themore » inventory is provided as annually varying estimates from years 1980–2012 and employs a source specific spatial scaling procedure. We estimate a global source in year 2012 of 406 Gg S y -1 (range of 223–586 Gg S y -1), which is highly concentrated in China and is twice as large as the previous gridded inventory. Our large upward revision in the bottom-up estimate of the source is consistent with a recent top-down estimate based on air-monitoring and Antarctic firn data. Furthermore, our inventory time trends, including a decline in the 1990's and growth after the year 2000, are qualitatively consistent with trends in atmospheric data. Lastly, similarities between the spatial distribution in this inventory and remote sensing data suggest that the anthropogenic source could potentially play a role in explaining a missing source in the global COS budget.« less
Global gridded anthropogenic emissions inventory of carbonyl sulfide
NASA Astrophysics Data System (ADS)
Zumkehr, Andrew; Hilton, Tim W.; Whelan, Mary; Smith, Steve; Kuai, Le; Worden, John; Campbell, J. Elliott
2018-06-01
Atmospheric carbonyl sulfide (COS or OCS) is the most abundant sulfur containing gas in the troposphere and is an atmospheric tracer for the carbon cycle. Gridded inventories of global anthropogenic COS are used for interpreting global COS measurements. However, previous gridded anthropogenic data are a climatological estimate based on input data that is over three decades old and are not representative of current conditions. Here we develop a new gridded data set of global anthropogenic COS sources that includes more source sectors than previously available and uses the most current emissions factors and industry activity data as input. Additionally, the inventory is provided as annually varying estimates from years 1980-2012 and employs a source specific spatial scaling procedure. We estimate a global source in year 2012 of 406 Gg S y-1 (range of 223-586 Gg S y-1), which is highly concentrated in China and is twice as large as the previous gridded inventory. Our large upward revision in the bottom-up estimate of the source is consistent with a recent top-down estimate based on air-monitoring and Antarctic firn data. Furthermore, our inventory time trends, including a decline in the 1990's and growth after the year 2000, are qualitatively consistent with trends in atmospheric data. Finally, similarities between the spatial distribution in this inventory and remote sensing data suggest that the anthropogenic source could potentially play a role in explaining a missing source in the global COS budget.
Reconstructing Contaminant Deposition in a San Francisco Bay Marina, California
Love, Adam H.; Esser, Bradley K.; Hunt, James R.
2010-01-01
Two sediment cores were collected from a marina in the San Francisco Bay to characterize historical sediment contamination resulting from the direct discharge of industrial wastewater from Naval Air Station Alameda. Depth profiles of trace metals, petroleum hydrocarbons, and radionuclides were determined with a 12-cm spacing down to a depth of 120 cm. The chronology of sediment accumulation is established by depth profiles of sedimentary time markers in conjunction with information on site history. The traditional approach of determining sediment accumulation rates by measuring atmospheric 210Pb deposition was obscured by a larger source of 210Pb in the sediments from the decay of anthropogenic 226Ra, likely from luminescent paints used at this facility and released to the marina. The sedimentation rates inferred from the data indicate that the greatest amount of contamination by trace metals and petroleum hydrocarbons took place between 1940 and 1960. In addition, anthropogenic 226Ra activities are positively correlated with some of the contaminants in the sediments, allowing the wastewater discharged from the facility to be distinguished from baywide contamination. In locations such as this, where there is a complex history of contaminant deposition, a source-specific tracer may be the only feasible method of attributing historical contamination to a point source. PMID:20333267
The nitrogen stable isotope, 15N, is an effective tool to track anthropogenic N sources to aquatic ecosystems. It may be difficult to identify potential N sources, however, where 15N responds similarly to multiple, concurrent activities in the watershed that cause higher nutrient...
Stable Isotope Evidence of Variation in Nitrogen Fixation by Cyanobacteria in Coastal Ecosystems
NASA Astrophysics Data System (ADS)
Paul, V.; Clementz, M.
2006-12-01
Increased nutrient loading via both natural and anthropogenic factors has been reported as one possible mechanism for the recent increase in the occurrence and intensity of harmful algal blooms (HAB) in coastal ecosystems. Influx of iron, phosphorous, and organic carbon have proven to be significant stimulating factors for HAB, since the benthic cyanobacteria that often make up these blooms are capable of nitrogen-fixation and require these nutrients for this process as well as photosynthesis. These cyanobacteria can switch to direct uptake of dissolved inorganic nitrogen (DIN), however, when concentrations are high enough to energetically favor this source, suggesting that high nitrogen input may also stimulate HAB. Given the distinct isotope differences between atmospheric N2 (0‰) and anthropogenic sources of DIN (>6‰), measurement of the δ15N composition of cyanobacteria can provide a means of gauging the relative significance of anthropogenic versus atmospheric nitrogen to the growth of these blooms. Likewise, the δ13C composition of these primary producers is controlled by the δ13C composition of the DIC, and can be a second tracer of anthropogenic influx into marine ecosystems. A combined approach using both isotope tracers was employed to determine the significance of anthropogenic nitrogen on HAB in subtropical/tropical coastal marine ecosystems. Samples of cyanobacteria and associated macroalgae were collected from three coastal sites in Guam (Facpi Point, Tanguisson, and Ypao Beach), one locality in Hawaii, and three sites in southern Florida (Pepper Park, Fort Lauderdale, Florida Keys). Following removal of marine carbonates via an acid rinse, the δ13C and δ15N values were determined for each species. Cyanobacterial δ15N values ranged from -2.3‰ to 7.7‰ with the highest values reported from sites in Guam. Only cyanobacteria sampled from Hawaii showed no isotope evidence of an anthropogenic source for nitrogen. A strong negative correlation between δ13C and δ15N values was detected for cyanobacteria from all sites. This correlation suggests that cyanobacteria are fixing nitrogen under oligotrophic conditions, but switch to using the readily available DIN when the nutrient load is high. The discovery of this relationship in three separate locations and among several different species of cyanobacteria suggests that this is a common feature of HAB and that nitrogen influx may have a more significant impact on the formation of these blooms than previously thought.
Anthropogenic rare earth elements and their spatial distributions in the Han River, South Korea.
Song, Hyeongseok; Shin, Woo-Jin; Ryu, Jong-Sik; Shin, Hyung Seon; Chung, Heesun; Lee, Kwang-Sik
2017-04-01
Rare earth elements (REE) consist of lanthanides (from La to Lu), together with yttrium and scandium, in which anthropogenic REE, such as gadolinium (Gd), lanthanum (La), and samarium (Sm), has emerged as micro-contaminants in natural waters in highly developed countries. Here, we collected water samples in the Han River (HR) and its tributaries flowing through Seoul Capital Area, the world's second largest metropolitan area in order to examine how and to what extent anthropogenic REE anomalies may occur. Water samples show higher light REE concentrations than heavy REE concentrations, while wastewater treatment plant (WWTP) samples display much higher heavy REE concentrations due to high Gd concentration. The PAAS-normalized REE patterns indicate that WWTP samples display the pronounced positive Gd anomalies, in which anthropogenic Gd from magnetic resonance imaging (MRI) diagnostic system occurs as a form of Gd complexation with either Cl - or SO 4 2- . Due to the WWTP, both the HR and tributaries show also positive Gd anomalies and the anthropogenic Gd concentrations increase as a function of the distance from the Paldang dam. This result indicates a positive correlation between populaton, number of MRI instruments, and positive Gd anomaly. Similarly, positive La and Sm anomalies exist in the HR, indicating that the HR is also affected by their point sources. Based on the discharge rate and anthropogenic REE concentrations, their fluxes are estimated to be 952 ± 319 kg/yr, suggesting that this amount of fluxes could disturb REE distribution in the Yellow Sea, and pose harmful effects on aquatic ecosystems. Copyright © 2016 Elsevier Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Jaars, Kerneels; Vestenius, Mika; van Zyl, Pieter G.; Beukes, Johan P.; Hellén, Heidi; Vakkari, Ville; Venter, Marcell; Josipovic, Miroslav; Hakola, Hannele
2018-01-01
Volatile organic compounds (VOCs) can have significant impacts on climate and human health. Certain VOCs are proven to be carcinogenic and toxic, which can affect human health directly and indirectly. In order to develop climate change reduction strategies and to assess the impacts of VOCs on human health, it is crucial to determine the sources of VOCs, which can be emitted from biogenic and anthropogenic sources. The aim of this study was to perform source apportionment using positive matrix factorisation (PMF) analysis on VOC data collected at a regional background location affected by the major sources in the interior of South Africa, which include the western- and eastern Bushveld Igneous Complex, the Johannesburg-Pretoria metropolitan conurbation, the Vaal Triangle, the Mpumalanga Highveld and also a region of anti-cyclonic recirculation of air mass over the interior of South Africa. In addition, a risk assessment study was also performed in view of the major source regions affecting Welgegund in order to quantify the impacts of anthropogenic VOCs measured at Welgegund on human health. Measurements were conducted at the Welgegund measurement station located on a commercial farm approximately 100 km west of Johannesburg for a period of more than two years. PMF analysis revealed ten meaningful factor solutions, of which five factors were associated with biogenic emissions and five with anthropogenic sources. Three of the biogenic factors were characterised by a specific biogenic species, i.e. isoprene, limonene and 2-methyl-3-buten-2-ol (MBO), while the other two biogenic factors comprised mixtures of biogenic species with different tracer species. The temporal factor contribution for the isoprene, limonene and MBO factors correlated relatively well with the seasonal wet pattern. One anthropogenic factor was associated with emissions from a densely populated anthropogenic source region to the east of Welgegund with a large number of industrial activities, while another anthropogenic factor could be related to coal combustion. An anthropogenic factor was also identified that reflected the influence of solvents on atmospheric VOC concentrations, while two anthropogenic factors were determined that indicated the influence of farming activities in close proximity to Welgegund. A lifetime cancer risk- (LCR) and non-cancer hazard ratio (HR) assessment study conducted for VOCs measured at Welgegund in relation to three source regions indicated that the non-cancerous influence of VOCs measured in the source regions is significantly lower compared to the cancerous influence of these species on human health, which raises concern. However, LCR values were within an acceptable range. Factor analysis performed in this paper also identified sources that could be targeted to minimise VOC-related LCRs and HRs e.g. benzene-related cancers can be reduced by targeting incomplete combustion sources and coal combustion.
NASA Astrophysics Data System (ADS)
Vystavna, Yuliya
2014-05-01
The research focuses on the monitoring of trace metals and pharmaceuticals as potential anthropogenic indicators of industrial and urban influences on surface water in poorly gauged transboundary Ukraine/Russia region. This study includes analysis of tracers use for the indication of water pollution events, including controlled and emerging discharges, and discussion of the detection method of these chemicals. The following criteria were proposed for the evaluation of indicators: specificity (physical chemical properties), variability (spatial and temporal) and practicality (capacity of the sampling and analytical techniques). The combination of grab and passive water sampling (i.e. DGT and POCIS) procedure was applied for the determination of dissolved and labile trace metals (Ag, Cd, Cr, Cu, Ni, Pb and Zn) and pharmaceuticals (carbamazepine, diazepam, paracetamol, caffeine, diclofenac and ketoprofen). Samples were analysed using ICP - MS (trace metals) and LC-MS/MS ESI +/- (pharmaceuticals). Our results demonstrate the distinctive spatial and temporal patterns of trace elements distribution along an urban watercourse. Accordingly, two general groups of trace metals have been discriminated: 'stable' (Cd and Cr) and 'time-varying' (Cu, Zn, Ni and Pb). The relationship Cd >> Cu > Ag > Cr ≥ Zn was proposed as an anthropogenic signature of the industrial and urban activities pressuring the environment from point sources (municipal wastewaters) and the group Pb - Ni was discussed as a relevant fingerprint of the economic activity (industry and transport) mainly from non-point sources (run-off, atmospheric depositions, etc.). Pharmaceuticals with contrasting hydro-chemical properties of molecules (water solubility, bioaccumulation, persistence during wastewater treatment processes) were discriminated on conservative, labile and with combined properties in order to provide information on wastewater treatment plant efficiency, punctual events (e.g. accidents on sewage works, run-off) and uncontrolled discharges. Applying mass balance modeling, medicaments were described as relevant socio-economic indicators, which can give a picture of main social aspects of the region.
Anthropogenic Carbon Pump in an Urbanized Estuary
NASA Astrophysics Data System (ADS)
Park, J. H.; Yoon, T. K.; Jin, H.; Begum, M. S.
2015-12-01
The importance of estuaries as a carbon source has been increasingly recognized over the recent decades. However, constraining sources of CO2 evasion from urbanized estuaries remains incomplete, particularly in densely populated river systems receiving high loads of organic carbon from anthropogenic sources. To account for major factors regulating carbon fluxes the tidal reach of the Han River estuary along the metropolitan Seoul, characterization of organic carbon in the main stem and major urban tributaries were combined with continuous, submersible sensor measurements of pCO2 at a mid-channel location over a year and continuous underway measurements using a submersible sensor and two equilibrator sytems across the estuarine section receiving urban streams. Single-site continuous measurements exhibited large seasonal and diurnal variations in pCO2, ranging from sub-ambient air levels to exceptionally high values approaching 10,000 ppm. Diurnal variations of pCO2 were pronounced in summer and had an inverse relationship with dissolved oxygen, pointing to a potential role of day-time algal consumption of CO2. Cruise measurements displayed sharp pCO2 pulses along the confluences of urban streams as compared with relatively low values along the upper estuary receiving low-CO2 outflows from upstream dams. Large downstream increases in pCO2, concurrent with increases in DOC concentrations and fluorescence intensities indicative of microbially processed organic components, imply a translocation and subsequent dilution of CO2 carried by urban streams and/or fast transformations of labile C during transit along downstream reaches. The unique combination of spatial and temporal continuous measurements of pCO2 provide insights on estuarine CO2 pulses that might have resulted from the interplay between high loads of CO2 and organic C of anthropogenic origin and their priming effects on estuarine microbial processing of terrigenous and algal organic matter.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Holdridge, D. J.
Global Warming and Methane--Global warming, an increase in Earth's near-surface temperature, is believed to result from the buildup of what scientists refer to as ''greenhouse gases.'' These gases include water vapor, carbon dioxide, methane, nitrous oxide, ozone, perfluorocarbons, hydrofluoro-carbons, and sulfur hexafluoride. Greenhouse gases can absorb outgoing infrared (heat) radiation and re-emit it back to Earth, warming the surface. Thus, these gases act like the glass of a greenhouse enclosure, trapping infrared radiation inside and warming the space. One of the more important greenhouse gases is the naturally occurring hydrocarbon methane. Methane, a primary component of natural gas, is themore » second most important contributor to the greenhouse effect (after carbon dioxide). Natural sources of methane include wetlands, fossil sources, termites, oceans, fresh-waters, and non-wetland soils. Methane is also produced by human-related (or anthropogenic) activities such as fossil fuel production, coal mining, rice cultivation, biomass burning, water treatment facilities, waste management operations and landfills, and domesticated livestock operations (Figure 1). These anthropogenic activities account for approximately 70% of the methane emissions to the atmosphere. Methane is removed naturally from the atmosphere in three ways. These methods, commonly referred to as sinks, are oxidation by chemical reaction with tropospheric hydroxyl ion, oxidation within the stratosphere, and microbial uptake by soils. In spite of their important role in removing excess methane from the atmosphere, the sinks cannot keep up with global methane production. Methane concentrations in the atmosphere have increased by 145% since 1800. Increases in atmospheric methane roughly parallel world population growth, pointing to anthropogenic sources as the cause (Figure 2). Increases in the methane concentration reduce Earth's natural cooling efficiency by trapping more of the outgoing terrestrial infrared radiation, increasing the near-surface temperature.« less
Saeedi, Mohsen; Li, Loretta Y; Salmanzadeh, Mahdiyeh
2012-08-15
50 street dust samples from four major streets in eastern and southern Tehran, the capital of Iran, were analyzed for metal pollution (Cu, Cr, Pb, Ni, Cd, Zn, Fe, Mn and Li). Hakanson's method was used to determine the Risk Index (RI) and ecological risks. Amongst these samples, 21 were also analyzed for polycyclic aromatic hydrocarbons (PAHs). Correlation, cluster and principal component analyses identified probable natural and anthropogenic sources of contaminants. The dust had elevated concentrations of Pb, Cd, Cu, Cr, Ni, Zn, Fe and PAHs. Enrichment factors of Cu, Pb, Cd and Zn showed that the dust is extremely enriched in these metals. Multivariate statistical analyses revealed that Cu, Pb, Zn, Fe and PAHs and, to a lesser extent, Cr and Ni have common anthropogenic sources. While Mn and Li were identified to have natural sources, Cd may have different anthropogenic origins. All samples demonstrated high ecological risk. Traffic and related activities, petrogenic and pyrogenic sources are likely to be the main anthropogenic sources of heavy metals and PAHs in Tehran dust. Copyright © 2012 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Kelly, Jamie M.; Doherty, Ruth M.; O'Connor, Fiona M.; Mann, Graham W.
2018-05-01
The global secondary organic aerosol (SOA) budget is highly uncertain, with global annual SOA production rates, estimated from global models, ranging over an order of magnitude and simulated SOA concentrations underestimated compared to observations. In this study, we use a global composition-climate model (UKCA) with interactive chemistry and aerosol microphysics to provide an in-depth analysis of the impact of each VOC source on the global SOA budget and its seasonality. We further quantify the role of each source on SOA spatial distributions, and evaluate simulated seasonal SOA concentrations against a comprehensive set of observations. The annual global SOA production rates from monoterpene, isoprene, biomass burning, and anthropogenic precursor sources is 19.9, 19.6, 9.5, and 24.6 Tg (SOA) a-1, respectively. When all sources are included, the SOA production rate from all sources is 73.6 Tg (SOA) a-1, which lies within the range of estimates from previous modelling studies. SOA production rates and SOA burdens from biogenic and biomass burning SOA sources peak during Northern Hemisphere (NH) summer. In contrast, the anthropogenic SOA production rate is fairly constant all year round. However, the global anthropogenic SOA burden does have a seasonal cycle which is lowest during NH summer, which is probably due to enhanced wet removal. Inclusion of the new SOA sources also accelerates the ageing by condensation of primary organic aerosol (POA), making it more hydrophilic, leading to a reduction in the POA lifetime. With monoterpene as the only source of SOA, simulated SOA and total organic aerosol (OA) concentrations are underestimated by the model when compared to surface and aircraft measurements. Model agreement with observations improves with all new sources added, primarily due to the inclusion of the anthropogenic source of SOA, although a negative bias remains. A further sensitivity simulation was performed with an increased anthropogenic SOA reaction yield, corresponding to an annual global SOA production rate of 70.0 Tg (SOA) a-1. Whilst simulated SOA concentrations improved relative to observations, they were still underestimated in urban environments and overestimated further downwind and in remote environments. In contrast, the inclusion of SOA from isoprene and biomass burning did not improve model-observations biases substantially except at one out of two tropical locations. However, these findings may reflect the very limited availability of observations to evaluate the model, which are primarily located in the NH mid-latitudes where anthropogenic emissions are high. Our results highlight that, within the current uncertainty limits in SOA sources and reaction yields, over the NH mid-latitudes, a large anthropogenic SOA source results in good agreement with observations. However, more observations are needed to establish the importance of biomass burning and biogenic sources of SOA in model agreement with observations.
Sources and Chemical Composition of Atmospheric Fine Particles in Rabigh, Saudi Arabia
NASA Astrophysics Data System (ADS)
Nayebare, S. R.; Aburizaiza, O. S.; Siddique, A.; Hussain, M. M.; Zeb, J.; Khwaja, H. A.
2014-12-01
Air pollution research in Saudi Arabia and the whole of Middle East is at its inception, making air pollution in the region a significant problem. This study presents the first detailed data on fine particulate matter (PM2.5) concentrations of Black Carbon (BC), ions, and trace metals at Rabigh, Saudi Arabia, and assesses their sources. Results showed several characteristic aspects of air pollution at Rabigh. Daily levels of PM2.5 and BC showed significant temporal variability ranging from 12.2 - 75.9 µg/m3 and 0.39 - 1.31 µg/m3, respectively. More than 90% of the time, the daily PM2.5 exceeded the 24 h WHO guideline of 20 µg/m3. Sulfate, NO3-, and NH4+ dominated the identifiable components. Trace metals with significantly higher concentrations included Si, S, Ca, Al, Fe, Na, Cl, Mg, K, and Ti, with average concentrations of 3.1, 2.2, 1.6, 1.2, 1.1, 0.7, 0.7, 0.5, 0.4 and 0.1 µg/m3, respectively. Based on the Air Quality Index (AQI), there were 44% days of moderate air quality, 33% days of unhealthy air quality for sensitive groups, and 23% days of unhealthy air quality throughout the study period. Two categories of aerosol trace metal sources were defined: anthropogenic (S, V, Cr, Ni, Cu, Zn, Br, Cd, Sb, and Pb) and naturally derived elements (Si, Al, and Fe). The extent of anthropogenic contribution was estimated by the degree of enrichment of these elements compared to the crustal composition. Soil resuspension and/or mobilization is an important source of "natural" elements, while "anthropogenic" elements originate primarily from fossil fuel combustion and industries. Ni and V correlated strongly pointing to combustion of heavy fuel oil as the likely source. A positive matrix factorization (PMF) was used to obtain information about possible sources. Our study highlights the need for stringent laws on PM2.5 emission control to protect human health and the environment.
Bjørn, Anders; Diamond, Miriam; Birkved, Morten; Hauschild, Michael Zwicky
2014-11-18
The ecological footprint method has been successful in communicating environmental impacts of anthropogenic activities in the context of ecological limits. We introduce a chemical footprint method that expresses ecotoxicity impacts from anthropogenic chemical emissions as the dilution needed to avoid freshwater ecosystem damage. The indicator is based on USEtox characterization factors with a modified toxicity reference point. Chemical footprint results can be compared to the actual dilution capacity within the geographic vicinity receiving the emissions to estimate whether its ecological limit has been exceeded and hence whether emissions can be expected to be environmentally sustainable. The footprint method was illustrated using two case studies. The first was all inventoried emissions from European countries and selected metropolitan areas in 2004, which indicated that the dilution capacity was likely exceeded for most European countries and all landlocked metropolitan areas. The second case study indicated that peak application of pesticides alone was likely to exceed Denmark's freshwater dilution capacity in 1999-2011. The uncertainty assessment showed that better spatially differentiated fate factors would be useful and pointed out other major sources of uncertainty and some opportunities to reduce these.
Coastal Seabed Mapping with Hyperspectral and Lidar data
NASA Astrophysics Data System (ADS)
Taramelli, A.; Valentini, E.; Filipponi, F.; Cappucci, S.
2017-12-01
A synoptic view of the coastal seascape and its dynamics needs a quantitative ability to dissect different components over the complexity of the seafloor where a mixture of geo - biological facies determines geomorphological features and their coverage. The present study uses an analytical approach that takes advantage of a multidimensional model to integrate different data sources from airborne Hyperspectral and LiDAR remote sensing and in situ measurements to detect antropogenic features and ecological `tipping points' in coastal seafloors. The proposed approach has the ability to generate coastal seabed maps using: 1) a multidimensional dataset to account for radiometric and morphological properties of waters and the seafloor; 2) a field spectral library to assimilate the high environmental variability into the multidimensional model; 3) a final classification scheme to represent the spatial gradients in the seafloor. The spatial pattern of the response to anthropogenic forcing may be indistinguishable from patterns of natural variability. It is argued that this novel approach to define tipping points following anthropogenic impacts could be most valuable in the management of natural resources and the economic development of coastal areas worldwide. Examples are reported from different sites of the Mediterranean Sea, both from Marine Protected and un-Protected Areas.
Source Separation and Treament of Anthropogenic Urine (WERF Report INFR4SG09b)
Abstract: Anthropogenic urine, although only 1% of domestic wastewater flow, is responsible for 50-80% of the nutrients and a substantial portion of the pharmaceuticals and hormones present in the influent to wastewater treatment plants. Source separation and treatment of urine...
MERCURY CONTROL FOR COAL-FIRED POWER PLANTS
There are many sources of natural and anthropogenic mercury emissions, but combustion of coal is known to be the major anthropogenic source of mercury (Hg) emissions in the U.S. and world wide. To address this, EPA has recently promulgated the Clean Air Mercury Rule to reduce Hg ...
The report documents the development of national- and state- level emissions estimates of radiatively important trace gases (RlTGs). Emissions estimates are presented for the principal anthropogenic sources of carbon dioxide (CO2), methane (CH4), chlorofluorocarbons (CFCs), and o...
Huang, Jinliang; Huang, Yaling; Zhang, Zhenyu
2014-01-01
Surface water samples of baseflow were collected from 20 headwater sub-watersheds which were classified into three types of watersheds (natural, urban and agricultural) in the flood, dry and transition seasons during three consecutive years (2010–2012) within a coastal watershed of Southeast China. Integrating spatial statistics with multivariate statistical techniques, river water quality variations and their interactions with natural and anthropogenic controls were examined to identify the causal factors and underlying mechanisms governing spatiotemporal patterns of water quality. Anthropogenic input related to industrial effluents and domestic wastewater, agricultural activities associated with the precipitation-induced surface runoff, and natural weathering process were identified as the potential important factors to drive the seasonal variations in stream water quality for the transition, flood and dry seasons, respectively. All water quality indicators except SRP had the highest mean concentrations in the dry and transition seasons. Anthropogenic activities and watershed characteristics led to the spatial variations in stream water quality in three types of watersheds. Concentrations of NH4 +-N, SRP, K+, CODMn, and Cl− were generally highest in urban watersheds. NO3 –N Concentration was generally highest in agricultural watersheds. Mg2+ concentration in natural watersheds was significantly higher than that in agricultural watersheds. Spatial autocorrelations analysis showed similar levels of water pollution between the neighboring sub-watersheds exhibited in the dry and transition seasons while non-point source pollution contributed to the significant variations in water quality between neighboring sub-watersheds. Spatial regression analysis showed anthropogenic controls played critical roles in variations of water quality in the JRW. Management implications were further discussed for water resource management. This research demonstrates that the coupled effects of natural and anthropogenic controls involved in watershed processes, contribute to the seasonal and spatial variation of headwater stream water quality in a coastal watershed with high spatial variability and intensive anthropogenic activities. PMID:24618771
Magner, J A; Brooks, K N
2008-03-01
Section 303(d) of the Clean Water Act requires States and Tribes to list waters not meeting water quality standards. A total maximum daily load must be prepared for waters identified as impaired with respect to water quality standards. Historically, the management of pollution in Minnesota has been focused on point-source regulation. Regulatory effort in Minnesota has improved water quality over the last three decades. Non-point source pollution has become the largest driver of conventional 303(d) listings in the 21st century. Conventional pollutants, i.e., organic, sediment and nutrient imbalances can be identified with poor land use management practices. However, the cause and effect relationship can be elusive because of natural watershed-system influences that vary with scale. Elucidation is complex because the current water quality standards in Minnesota were designed to work best with water quality permits to control point sources of pollution. This paper presents a sentinel watershed-systems approach (SWSA) to the monitoring and assessment of Minnesota waterbodies. SWSA integrates physical, chemical, and biological data over space and time using advanced technologies at selected small watersheds across Minnesota to potentially improve understanding of natural and anthropogenic watershed processes and the management of point and non-point sources of pollution. Long-term, state-of-the-art monitoring and assessment is needed to advance and improve water quality standards. Advanced water quality or ecologically-based standards that integrate physical, chemical, and biological numeric criteria offer the potential to better understand, manage, protect, and restore Minnesota's waterbodies.
Rushdi, Ahmed I; Al-Mutlaq, Khalid F; El-Mubarak, Aarif H; Al-Saleh, Mohammed A; El-Otaibi, Mubarak T; Ibrahim, Sami M M; Simoneit, Bernd R T
2016-01-01
Soil particles contain a variety of natural and anthropogenic organic components, and in urban areas can be considered as local collectors of pollutants. Surface soil samples were taken from ten urban areas in Riyadh during early winter of 2007. They were extracted with dichloromethane-methanol mixture and the extracts were analyzed by gas chromatography-mass spectrometry. The major compounds were unresolved complex mixture (UCM), plasticizers, n-alkanes, carbohydrates, n-alkanoic acids, hopanes, n-alkanols, and sterols. Vegetation detritus was the major natural source of organic compounds (24.0 ± 15.7%) in samples from areas with less human activities and included n-alkanes, n-alkanoic acids, n-alkanols, sterols and carbohydrates. Vehicular emission products and discarded plastics were the major anthropogenic sources in the soil particles (53.3 ± 21.3% and 22.7 ± 10.7%, respectively). The anthropogenic tracers were UCM, plasticizers, n-alkanes, hopanes and traces of steranes. Vegetation and human activities control the occurrence and distribution of natural and anthropogenic extractable organic matter in this arid urban area. Copyright © 2015 Elsevier Ltd. All rights reserved.
Methane sources in Hong Kong - identification by mobile measurement and isotopic analysis
NASA Astrophysics Data System (ADS)
Fisher, Rebecca; Brownlow, Rebecca; Lowry, David; Lanoisellé, Mathias; Nisbet, Euan
2017-04-01
Hong Kong (22.4°N, 114.1°E) has a wide variety of natural and anthropogenic sources of methane within a small densely populated area (1106 km2, population ˜7.3 million). These include emissions from important source categories that have previously been poorly studied in tropical regions such as agriculture and wetlands. According to inventories (EDGAR v.4.2) anthropogenic methane emissions are mainly from solid waste disposal, wastewater disposal and fugitive leaks from oil and gas. Methane mole fraction was mapped out across Hong Kong during a mobile measurement campaign in July 2016. This technique allows rapid detection of the locations of large methane emissions which may focus targets for efforts to reduce emissions. Methane is mostly emitted from large point sources, with highest concentrations measured close to active landfill sites, sewage works and a gas processing plant. Air samples were collected close to sources (landfills, sewage works, gas processing plant, wetland, rice, traffic, cows and water buffalo) and analysed by mass spectrometry to determine the δ13C isotopic signatures to extend the database of δ13C isotopic signatures of methane from tropical regions. Isotopic signatures of methane sources in Hong Kong range from -70 ‰ (cows) to -37 ‰ (gas processing). Regular sampling of air for methane mole fraction and δ13C has recently begun at the Swire Institute of Marine Science, situated at Cape d'Aguilar in the southeast of Hong Kong Island. This station receives air from important source regions: southerly marine air from the South China Sea in summer and northerly continental air in winter and measurements will allow an integrated assessment of emissions from the wider region.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Turner, A. J.; Jacob, D. J.; Wecht, K. J.
2015-02-18
We use 2009–2011 space-borne methane observations from the Greenhouse Gases Observing SATellite (GOSAT) to constrain global and North American inversions of methane emissions with 4° × 5° and up to 50 km × 50 km spatial resolution, respectively. The GOSAT data are first evaluated with atmospheric methane observations from surface networks (NOAA, TCCON) and aircraft (NOAA/DOE, HIPPO), using the GEOS-Chem chemical transport model as a platform to facilitate comparison of GOSAT with in situ data. This identifies a high-latitude bias between the GOSAT data and GEOS-Chem that we correct via quadratic regression. The surface and aircraft data are subsequently usedmore » for independent evaluation of the methane source inversions. Our global adjoint-based inversion yields a total methane source of 539 Tg a −1 and points to a large East Asian overestimate in the EDGARv4.2 inventory used as a prior. Results serve as dynamic boundary conditions for an analytical inversion of North American methane emissions using radial basis functions to achieve high resolution of large sources and provide full error characterization. We infer a US anthropogenic methane source of 40.2–42.7 Tg a −1, as compared to 24.9–27.0 Tg a −1 in the EDGAR and EPA bottom-up inventories, and 30.0–44.5 Tg a −1 in recent inverse studies. Our estimate is supported by independent surface and aircraft data and by previous inverse studies for California. We find that the emissions are highest in the South-Central US, the Central Valley of California, and Florida wetlands, large isolated point sources such as the US Four Corners also contribute. We attribute 29–44% of US anthropogenic methane emissions to livestock, 22–31% to oil/gas, 20% to landfills/waste water, and 11–15% to coal with an additional 9.0–10.1 Tg a −1 source from wetlands.« less
Hu, Yuanan; Cheng, Hefa
2016-07-01
Quantification of the contributions from anthropogenic sources to soil heavy metal loadings on regional scales is challenging because of the heterogeneity of soil parent materials and high variability of anthropogenic inputs, especially for the species that are primarily of lithogenic origin. To this end, we developed a novel method for apportioning the contributions of natural and anthropogenic sources by combining sequential extraction and stochastic modeling, and applied it to investigate the heavy metal pollution in the surface soils of the Pearl River Delta (PRD) in southern China. On the average, 45-86% of Zn, Cu, Pb, and Cd were present in the acid soluble, reducible, and oxidizable fractions of the surface soils, while only 12-24% of Ni, Cr, and As were partitioned in these fractions. The anthropogenic contributions to the heavy metals in the non-residual fractions, even the ones dominated by natural sources, could be identified and quantified by conditional inference trees. Combination of sequential extraction, Kriging interpolation, and stochastic modeling reveals that approximately 10, 39, 6.2, 28, 7.1, 15, and 46% of the As, Cd, Cr, Cu, Ni, Pb, and Zn, respectively, in the surface soils of the PRD were contributed by anthropogenic sources. These results were in general agreements with those obtained through subtraction of regional soil metal background from total loadings, and the soil metal inputs through atmospheric deposition as well. In the non-residual fractions of the surface soils, the anthropogenic contributions to As, Cd, Cr, Cu, Ni, Pb, and Zn, were 48, 42, 50, 51, 49, 24, and 70%, respectively. Copyright © 2016 Elsevier Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Harker, Leslie; Hutcheon, Ian; Mayer, Bernhard
2015-11-01
The Kettle River Basin in South central British Columbia (Canada) is under increasing anthropogenic pressures affecting both water quantity and quality of surface waters and aquifers. We investigated water quality and sources and processes influencing NO3- and SO42- in the Kettle River Basin using a combination of chemical and isotopic techniques. The dominant water type in the Kettle River Basin is Ca-HCO3 with surface waters having total dissolved solids (TDS) concentrations of < 115 mg/L and groundwaters having TDS values of up to 572 mg/L. Based on δ15NNO3andδ18ONO3 values and concentration data, NO3- in surface waters originates primarily from natural soil nitrification processes, with additional influences from anthropogenic activities, such as waste water effluents at sampling locations downstream from population centres. The source of NO3- in groundwater was predominantly nitrification of soil organic matter, although nitrate in a few groundwater samples originated from anthropogenic sources, including manure or septic systems. The dominant source of SO42- in surface water and groundwater samples was the natural oxidation of sulfide minerals. With increasing distance downstream, surface water δ18OSO4 values increase beyond the range of oxidation of sulfide minerals and into the range of soil and atmospheric-derived SO42- that is in part derived from anthropogenic emissions. Hence, we conclude that recent anthropogenic impacts have affected water quality only marginally at only few sites in the Kettle River Basin. The presented data will serve as an excellent baseline against which future impacts can be assessed.
Crustal materials are mainly emitted by anthropogenic and windblown fugitive dust, but also may potentially include some fly ash and industrial process emissions which are chemically similar to crustal emissions. Source apportionment studies have shown that anthropogenic fugitive...
Estimation of mercury emission from different sources to atmosphere in Chongqing, China.
Wang, Dingyong; He, Lei; Wei, Shiqiang; Feng, Xinbin
2006-08-01
This investigation presents a first assessment of the contribution to the regional mercury budget from anthropogenic and natural sources in Chongqing, an important industrial region in southwest China. The emissions of mercury to atmosphere from anthropogenic sources in the region were estimated through indirect approaches, i.e. using commonly acceptable emission factors method, which based on annual process throughputs or consumption for these sources. The natural mercury emissions were estimated from selected natural sources by the dynamic flux chamber technique. The results indicated that the anthropogenic mercury emissions totaled approximately 8.85 tons (t), more than 50% of this total originated in coal combustion and 23.7% of this total emission in the industrial process (include cement production, metal smelting and chemical industry). The natural emissions represented approximately 17% of total emissions (1.78 t yr(-1)). The total mercury emission to atmosphere in Chongqing in 2001 was 10.63 t.
Han, Li; Wang, Xing-Rui; He, Min; Guo, Wei-Guang
2013-12-01
Based on Sichuan province environmental statistical survey data and other relevant activity data, volatile organic compounds (VOCs) emissions from typical anthropogenic sources in Sichuan province were calculated for the year of 2011 by applying the emission factor method. Besides, ozone and secondary organic aerosol formation potentials of these typical anthropogenic sources were discussed. The total VOC emission from these sources was about 482 kt in Sichuan province, biomass burning, solvent utilization, industrial processes, storage and distribution of fuel, and fossil fuel combustion contributed 174 kt, 153 kt, 121 kt, 21 kt and 13 kt, respectively; architecture wall painting, furniture coating, wood decoration painting and artificial board were the major emission sectors of the solvent utilization; while for the industrial processes, 19.4% of VOCs emission was from the wine industry. Chengdu was the largest contributor compared to the other cities in Sichuan, whose VOCs emission from these typical anthropogenic sources in 2011 was 112 kt. OFP of these sources was 1,930 kt altogether. Solvent utilization contributed 50.5% of the total SOA formation potentials, biomass burning and industrial processes both contributed about 23% , with storage and distribution of fuel and fossil fuel combustion accounting for 1% and 1.4%, respectively.
Atmospheric inverse modeling via sparse reconstruction
NASA Astrophysics Data System (ADS)
Hase, Nils; Miller, Scot M.; Maaß, Peter; Notholt, Justus; Palm, Mathias; Warneke, Thorsten
2017-10-01
Many applications in atmospheric science involve ill-posed inverse problems. A crucial component of many inverse problems is the proper formulation of a priori knowledge about the unknown parameters. In most cases, this knowledge is expressed as a Gaussian prior. This formulation often performs well at capturing smoothed, large-scale processes but is often ill equipped to capture localized structures like large point sources or localized hot spots. Over the last decade, scientists from a diverse array of applied mathematics and engineering fields have developed sparse reconstruction techniques to identify localized structures. In this study, we present a new regularization approach for ill-posed inverse problems in atmospheric science. It is based on Tikhonov regularization with sparsity constraint and allows bounds on the parameters. We enforce sparsity using a dictionary representation system. We analyze its performance in an atmospheric inverse modeling scenario by estimating anthropogenic US methane (CH4) emissions from simulated atmospheric measurements. Different measures indicate that our sparse reconstruction approach is better able to capture large point sources or localized hot spots than other methods commonly used in atmospheric inversions. It captures the overall signal equally well but adds details on the grid scale. This feature can be of value for any inverse problem with point or spatially discrete sources. We show an example for source estimation of synthetic methane emissions from the Barnett shale formation.
Barium as a potential indicator of phosphorus in agricultural runoff.
Ahlgren, Joakim; Djodjic, Faruk; Wallin, Mats
2012-01-01
In many catchments, anthropogenic input of contaminants, and in particular phosphorus (P), into surface water is a mixture of agricultural and sewage runoff. Knowledge about the relative contribution from each of these sources is vital for mitigation of major environmental problems such as eutrophication. In this study, we investigated whether the distribution of trace elements in surface waters can be used to trace the contamination source. Water from three groups of streams was investigated: streams influenced only by agricultural runoff, streams influenced mainly by sewage runoff, and reference streams. Samples were collected at different flow regimes and times of year and analyzed for 62 elements using ICP-MS. Our results show that there are significant differences between the anthropogenic sources affecting the streams in terms of total element composition and individual elements, indicating that the method has the potential to trace anthropogenic impact on surface waters. The elements that show significant differences between sources are strontium (p < 0.001), calcium (p < 0.004), potassium (p < 0.001), magnesium (p < 0.001), boron (p < 0.001), rhodium (p = 0.001), and barium (p < 0.001). According to this study, barium shows the greatest potential as a tracer for an individual source of anthropogenic input to surface waters. We observed a strong relationship between barium and total P in the investigated samples (R(2) = 0.78), which could potentially be used to apportion anthropogenic sources of P and thereby facilitate targeting of mitigation practices. Copyright © by the American Society of Agronomy, Crop Science Society of America, and Soil Science Society of America, Inc.
NASA Astrophysics Data System (ADS)
Yuan, Bin; Shao, Min; de Gouw, Joost; Parrish, David D.; Lu, Sihua; Wang, Ming; Zeng, Limin; Zhang, Qian; Song, Yu; Zhang, Jianbo; Hu, Min
2012-12-01
Volatile organic compounds (VOCs) were measured online at an urban site in Beijing in August-September 2010. Diurnal variations of various VOC species indicate that VOCs concentrations were influenced by photochemical removal with OH radicals for reactive species and secondary formation for oxygenated VOCs (OVOCs). A photochemical age-based parameterization method was applied to characterize VOCs chemistry. A large part of the variability in concentrations of both hydrocarbons and OVOCs was explained by this method. The determined emission ratios of hydrocarbons to acetylene agreed within a factor of two between 2005 and 2010 measurements. However, large differences were found for emission ratios of some alkanes and C8 aromatics between Beijing and northeastern United States secondary formation from anthropogenic VOCs generally contributed higher percentages to concentrations of reactive aldehydes than those of inert ketones and alcohols. Anthropogenic primary emissions accounted for the majority of ketones and alcohols concentrations. Positive matrix factorization (PMF) was also used to identify emission sources from this VOCs data set. The four resolved factors were three anthropogenic factors and a biogenic factor. However, the anthropogenic factors are attributed here to a common source at different stages of photochemical processing rather than three independent sources. Anthropogenic and biogenic sources of VOCs concentrations were not separated completely in PMF. This study indicates that photochemistry of VOCs in the atmosphere complicates the information about separated sources that can be extracted from PMF and the influence of photochemical processing must be carefully considered in the interpretation of source apportionment studies based upon PMF.
Mercury emissions data from anthropogenic sources as described in Xu et al., 2016.This dataset is associated with the following publication:Xu, X., N. Liu, M. Landis, X. Feng, and G. Qiu. Characteristics and distributions of atmospheric mercury emitted from anthropogenic sources in Guiyang, southwestern China. Acta Geochimica. Springer, Heidelburg, GERMANY, 1-11, (2016).
Mahmoud, Shereif H; Gan, Thian Y
2018-08-15
The implications of anthropogenic climate change, human activities and land use change (LUC) on the environment and ecosystem services in the coastal regions of Saudi Arabia were analyzed. Earth observations data was used to drive land use categories between 1970 and 2014. Next, a Markov-CA model was developed to characterize the dynamic of LUC between 2014 and 2100 and their impacts on regions' climate and environment. Non-parametric change point and trend detection algorithms were applied to temperature, precipitation and greenhouse gases data to investigate the presence of anthropogenic climate change. Lastly, climate models were used to project future climate change between 2014 and 2100. The analysis of LUC revealed that between 1970 and 2014, built up areas experienced the greatest growth during the study period, leading to a significant monotonic trend. Urban areas increased by 2349.61km 2 between 1970 and 2014, an average increase of >53.4km 2 /yr. The projected LUC between 2014 and 2100 indicate a continued increase in urban areas and irrigated cropland. Human alteration of land use from natural vegetation and forests to other uses after 1970, resulted in a loss, degradation, and fragmentation, all of which usually have devastating effects on the biodiversity of the region. Resulting in a statistically significant change point in temperature anomaly after 1968 with a warming trend of 0.24°C/decade and a downward trend in precipitation anomaly of 12.2mm/decade. Total greenhouse gas emissions including all anthropogenic sources showed a statistically significant positive trend of 78,090Kt/decade after 1991. This is reflected in the future projection of temperature anomaly between 1900 and 2100 with a future warming trend of 0.19°C/decade. In conclusion, human activities, industrial revelation, deforestation, land use transformation and increase in greenhouse gases had significant implications on the environment and ecosystem services of the study area. Copyright © 2018 Elsevier B.V. All rights reserved.
Schuster, Paul F.; Krabbenhoft, David P.; Naftz, David L.; Cecil, L. DeWayne; Olson, Mark L.; DeWild, John F.; Susong, David D.; Green, Jaromy R.; Abbott, Michael L.
2002-01-01
Mercury (Hg) contamination of aquatic ecosystems and subsequent methylmercury bioaccumulation are significant environmental problems of global extent. At regional to global scales, the primary mechanism of Hg contamination is atmospheric Hg transport. Thus, a better understanding of the long-term history of atmospheric Hg cycling and quantification of the sources is critical for assessing the regional and global impact of anthropogenic Hg emissions. Ice cores collected from the Upper Fremont Glacier (UFG), Wyoming, contain a high-resolution record of total atmospheric Hg deposition (ca. 1720−1993). Total Hg in 97 ice-core samples was determined with trace-metal clean handling methods and low-level analytical procedures to reconstruct the first and most comprehensive atmospheric Hg deposition record of its kind yet available from North America. The record indicates major atmospheric releases of both natural and anthropogenic Hg from regional and global sources. Integrated over the past 270-year ice-core history, anthropogenic inputs contributed 52%, volcanic events 6%, and background sources 42%. More significantly, during the last 100 years, anthropogenic sources contributed 70% of the total Hg input. Unlike the 2−7-fold increase observed from preindustrial times (before 1840) to the mid-1980s in sediment-core records, the UFG record indicates a 20-fold increase for the same period. The sediment-core records, however, are in agreement with the last 10 years of this ice-core record, indicating declines in atmospheric Hg deposition.
Sedláček, Jan; Bábek, Ondřej; Nováková, Tereza
2017-01-01
While numerous studies of dam reservoirs contamination are reported world-wide, we present a missing link in the study of reservoirs sourced from multiple river catchments. In such reservoirs, different point sources of contaminants and variable composition of their sedimentary matrices add to extremely complex geochemical patterns. We studied a unique, step-wise filled Nové Mlýny dam reservoir, Czech Republic, which consists of three interconnected sub-basins. Their source areas are located in units with contrasting geology and different levels and sources of contamination. The aim of this study is to provide an insight into the provenance of the sediment, including lithogenic elements and anthropogenic pollutants, to investigate the sediment dispersal across the reservoir, and to assess the heavy metal pollution in each basin. The study is based on multi-proxy stratigraphic analysis and geochemistry of sediment cores. There is a considerable gradient in the sediment grain size, brightness, MS and geochemistry, which reflects changing hydrodynamic energy conditions and primary pelagic production of CaCO 3 . The thickness of sediments generally decreases from proximal to distal parts, but underwater currents can accumulate higher amounts of sediments in distal parts near the thalweg line. Average sedimentation rates vary over a wide range from 0.58cm/yr to 2.33cm/yr. In addition, the petrophysical patterns, concentrations of lithogenic elements and their ratios made it possible to identify two main provenance areas, the Dyje River catchment (upper basin) and the Svratka and Jihlava River catchments (middle and lower basin). Enrichment factors (EF) were used for distinguishing the anthropogenic element contribution from the local background levels. We found moderate Zn and Cu pollution (EF ~2 to 5) in the upper basin and Zn, Cu and Pb (EF ~2 to 4.5) in the middle basin with the peak contamination in the late 1980s, indicating that the two basins have different contamination histories. Copyright © 2016 Elsevier B.V. All rights reserved.
Detection of anthropogenic dust using CALIPSO lidar measurements
NASA Astrophysics Data System (ADS)
Huang, J. P.; Liu, J. J.; Chen, B.; Nasiri, S. L.
2015-10-01
Anthropogenic dusts are those produced by human activities on disturbed soils, which are mainly cropland, pastureland, and urbanized regions, and are a subset of the total dust load which includes natural sources from desert regions. Our knowledge of anthropogenic dusts is still very limited due to a lack of data. To understand the contribution of anthropogenic dust to the total global dust load, it is important to identify it apart from total dust. In this study, a new technique for distinguishing anthropogenic dust from natural dust is proposed by using Cloud-Aerosol Lidar and Infrared Pathfinder Satellite Observation (CALIPSO) dust and planetary boundary layer (PBL) height retrievals along with a land use data set. Using this technique, the global distribution of dust is analyzed and the relative contribution of anthropogenic and natural dust sources to regional and global emissions are estimated. Results reveal that local anthropogenic dust aerosol due to human activity, such as agriculture, industrial activity, transportation, and overgrazing, accounts for about 25 % of the global continental dust load. Of these anthropogenic dust aerosols, more than 53 % come from semi-arid and semi-wet regions. Annual mean anthropogenic dust column burden (DCB) values range from 0.42 g m-2, with a maximum in India, to 0.12 g m-2, with a minimum in North America. A better understanding of anthropogenic dust emission will enable us to focus on human activities in these critical regions and with such knowledge we will be more able to improve global dust models and to explore the effects of anthropogenic emission on radiative forcing, climate change, and air quality in the future.
NASA Astrophysics Data System (ADS)
Shuler, C. K.; El-Kadi, A. I.; Dulaiova, H.; Glenn, C. R.; Fackrell, J.
2015-12-01
The quality of municipal groundwater supplies on Tutuila, the main island in American Samoa, is currently in question. A high vulnerability for contamination from surface activities has been recognized, and there exists a strong need to clearly identify anthropogenic sources of pollution and quantify their influence on the aquifer. This study examines spatial relationships and time series measurements of nutrients and other tracers to identify predominant pollution sources and determine the water quality impacts of the island's diverse land uses. Elevated groundwater nitrate concentrations are correlated with areas of human development, however, the mixture of residential and agricultural land use in this unique village based agrarian setting makes specific source identification difficult using traditional geospatial analysis. Spatial variation in anthropogenic impact was assessed by linking NO3- concentrations and δ15N(NO3) from an extensive groundwater survey to land-use types within well capture zones and groundwater flow-paths developed with MODFLOW, a numerical groundwater model. Land use types were obtained from high-resolution GIS data and compared to water quality results with multiple-regression analysis to quantify the impact that different land uses have on water quality. In addition, historical water quality data and new analyses of δD and δ18O in precipitation, groundwater, and mountain-front recharge waters were used to constrain the sources and mechanisms of contamination. Our analyses indicate that groundwater nutrient levels on Tutuila are controlled primarily by residential, not agricultural activity. Also a lack of temporal variation suggests that episodic pollution events are limited to individual water sources as opposed to the entire aquifer. These results are not only valuable for water quality management on Tutuila, but also provide insight into the sustainability of groundwater supplies on other islands with similar hydrogeology and land use history.
Historical and Future Trends in Global Source-receptor Relationships of Mercury
NASA Astrophysics Data System (ADS)
Chen, L.; Zhang, W.; Wang, X.
2017-12-01
Growing concerns about the risk associated with increasing environmental Mercury (Hg) levels have resulted in a focus on the relationships between intercontinental emitted and accumulated Hg. We use a global biogeochemical Hg model with eight continental regions and a global ocean to evaluate the legacy impacts of historical anthropogenic releases (2000 BC to 2008 AD) on global source-receptor relationships of Hg. The legacy impacts of historical anthropogenic releases are confirmed to be significant on the source-receptor relationships according to our results. Historical anthropogenic releases from Asia account for 8% of total soil Hg in North America, which is smaller than the proportion ( 17%) from previous studies. The largest contributors to the global oceanic Hg are historical anthropogenic releases from North America (26%), Asia (16%), Europe (14%) and South America (14%). Although anthropogenic releases from Asia have exceeded North America since the 1970s, source contributions to global Hg receptors from Asia have not exceeded North America so far. Future projections indicate that if Hg emissions are not effectively controlled, Asia will exceed North America as the largest contributor to the global ocean in 2019 and this has a long-term adverse impact on the future environment. For the Arctic Ocean, historical anthropogenic release from North America contributes most to the oceanic Hg reservoir and future projections reveal that the legacy impacts of historical releases from mid-latitudes would lead to the potential of rising Hg in the Arctic Ocean in the future decades, which calls for more effective Hg controls on mid-latitude releases.
Historical and future trends in global source-receptor relationships of mercury.
Chen, Long; Zhang, Wei; Zhang, Yanxu; Tong, Yindong; Liu, Maodian; Wang, Huanhuan; Xie, Han; Wang, Xuejun
2018-01-01
Growing concern about the risk associated with increasing environmental mercury (Hg) concentrations has resulted in a focus on the relationships between intercontinental emitted and accumulated Hg. We use a global biogeochemical Hg model with 8 continental regions and a global ocean to evaluate the legacy impacts of historical anthropogenic releases (2000BCE to 2008AD) on global source-receptor relationships of Hg. Legacy impacts of historical anthropogenic releases are confirmed to be significant on the source-receptor relationships according to our results. Historical anthropogenic releases from Asia account for 8% of total soil Hg in North America, which is smaller than the proportion (~17%) from previous studies. The largest contributors to the global oceanic Hg are historical anthropogenic releases from North America (26%), Asia (16%), Europe (14%) and South America (14%). Although anthropogenic releases from Asia have exceeded North America since the 1970s, source contributions to global Hg receptors from Asia have not exceeded North America so far. Future projections indicate that if Hg emissions are not effectively controlled, Asia will exceed North America as the largest contributor to the global ocean in 2019 and this has a long-term adverse impact on the future environment. For the Arctic Ocean, historical anthropogenic release from North America contributes most to the oceanic Hg reservoir and future projections reveal that the legacy impacts of historical releases from mid-latitudes would lead to the potential of rising Hg in the Arctic Ocean in the future decades, which calls for more effective Hg controls on mid-latitude releases. Copyright © 2017 Elsevier B.V. All rights reserved.
Watershed development and anthropogenic sources of nitrogen are among leading causes of negative impacts to aquatic ecosystems around the world. The δ15N of aquatic biota can be used as indicators of anthropogenic sources of nitrogen enriched in 15N, but this mostly has bee...
NASA Astrophysics Data System (ADS)
Hissler, Christophe; Stille, Peter; Pfister, Laurent
2017-04-01
The sustainable management of water resources is one of the greatest challenges of the 21st century. Water is a vital resource that is increasingly put under pressure from multiple perspectives. While the global population is on the rise, socio-economic development makes equally rapid progress - eventually compromising access to clean water bodies. Multiple pollution sources constitute an immediate threat to aquatic ecosystems and are likely to cause long lasting contaminations of water bodies that are critical for drinking and/or irrigation water production. There is a pressing need for an adequate quantification of anthropogenic impacts on the critical zone of river basins and the identification of the temporal dynamics of these impacts. As an example, despite the work done to assess the environmental impact of REE pollutions in larger river systems, we are still lacking information on the dynamics of these anthropogenic compounds in relation to rapid hydrological changes. Filling these knowledge gaps is a pre-requisite for the design and implementation of sustainable water resources management strategies. In order to better constrain the relative contributions of both anthropogenic and geogenic trace element sources we propose using a multitracer approach combining elemental and 87Sr/86Sr, 143Nd/144Nd, and 206Pb/207Pb isotopic ratios. The use of these three separate isotopic systems together with REE concentrations is new in the field of anthropogenic source identification in river systems. We observed enrichments in Anthropogenic Rare Earth Elements (AREE) for dissolved Gd and suspended Nd loads of river water. With increasing discharge, AREE anomalies progressively disappeared and gave way to the geogenic chemical signature of the basin in both dissolved and suspended loads. The isotopic data confirm these observations and shed new light on the trace elements sources. On the one hand, dissolved loads have peculiar isotopic characteristics and carry mainly limestone-derived and anthropogenic Sr and Nd as well as significant amounts of anthropogenic Pb. On the other hand, the results clearly indicate that anthropogenic contributions impact the suspended loads in all hydrological conditions. This study demonstrates that (i) the composition of the AREE pool is characteristic of a given river basin and controlled by the different anthropogenic contributions located in a specific study area and (ii) the anthropogenic contributions to the river may change not only Pb, but also Sr and Nd isotopic compositions in both dissolved and suspended loads. This is of importance for future provenance studies in the critical zone of polluted river basins.
An evaluation of catchment-scale phosphorus mitigation using load apportionment modelling.
Greene, S; Taylor, D; McElarney, Y R; Foy, R H; Jordan, P
2011-05-01
Functional relationships between phosphorus (P) discharge and concentration mechanisms were explored using a load apportionment model (LAM) developed for use in a freshwater catchment in Ireland with fourteen years of data (1995-2008). The aim of model conceptualisation was to infer changes in point and diffuse sources from catchment P loading during P mitigation, based upon a dataset comprising geospatial and water quality data from a 256km(2) lake catchment in an intensively farmed drumlin region of the midlands of Ireland. The model was calibrated using river total P (TP), molybdate reactive P (MRP) and runoff data from seven subcatchments. Temporal and spatial heterogeneity of P sources existed within and between subcatchments; these were attributed to differences in agricultural intensity, soil type and anthropogenically-sourced effluent P loading. Catchment rivers were sensitive to flow regime, which can result in eutrophication of rivers during summer and lake enrichment from frequent flood events. For one sewage impacted river, the LAM estimated that point sourced P contributed up to of 90% of annual MRP load delivered during a hydrological year and in this river point P sources dominated flows up to 92% of days. In the other rivers, despite diffuse P forming a majority of the annual P exports, point sources of P dominated flows for up to 64% of a hydrological year. The calibrated model demonstrated that lower P export rates followed specific P mitigation measures. The LAM estimated up to 80% decreases in point MRP load after enhanced P removal at waste water treatments plants in urban subcatchments and the implementation of septic tank and agricultural bye-laws in rural subcatchments. The LAM approach provides a way to assess the long-term effectiveness of further measures to reduce P loadings in EU (International) River Basin Districts and subcatchments. Copyright © 2011 Elsevier B.V. All rights reserved.
Álvarez-Iglesias, P; Rubio, B; Millos, J
2012-10-15
San Simón Bay, the inner part of the Ría de Vigo (NW Spain), an area previously identified as highly polluted by Pb, was selected for the application of Pb stable isotope ratios as a fingerprinting tool in subtidal and intertidal sediment cores. Lead isotopic ratios were determined by inductively coupled plasma mass spectrometry on extracts from bulk samples after total acid digestion. Depth-wise profiles of (206)Pb/(207)Pb, (206)Pb/(204)Pb, (207)Pb/(204)Pb, (208)Pb/(204)Pb and (208)Pb/(207)Pb ratios showed, in general, an upward decrease for both intertidal and subtidal sediments as a consequence of the anthropogenic activities over the last century, or centuries. Waste channel samples from a nearby ceramic factory showed characteristic Pb stable isotope ratios different from those typical of coal and petrol. Natural isotope ratios from non-polluted samples were established for the study area, differentiating sediments from granitic or schist-gneiss sources. A binary mixing model employed on the polluted samples allowed estimating the anthropogenic inputs to the bay. These inputs represented between 25 and 98% of Pb inputs in intertidal samples, and 9-84% in subtidal samples, their contributions varying with time. Anthropogenic sources were apportioned according to a three-source model. Coal combustion-related emissions were the main anthropogenic source Pb to the bay (60-70%) before the establishment of the ceramic factory in the area (in the 1970s) which has since constituted the main source (95-100%), followed by petrol-related emissions. The Pb inputs history for the intertidal area was determined for the 20th century, and, for the subtidal area, the 19th and 20th centuries. Copyright © 2012 Elsevier B.V. All rights reserved.
Explosion localization and characterization via infrasound using numerical modeling
NASA Astrophysics Data System (ADS)
Fee, D.; Kim, K.; Iezzi, A. M.; Matoza, R. S.; Jolly, A. D.; De Angelis, S.; Diaz Moreno, A.; Szuberla, C.
2017-12-01
Numerous methods have been applied to locate, detect, and characterize volcanic and anthropogenic explosions using infrasound. Far-field localization techniques typically use back-azimuths from multiple arrays (triangulation) or Reverse Time Migration (RTM, or back-projection). At closer ranges, networks surrounding a source may use Time Difference of Arrival (TDOA), semblance, station-pair double difference, etc. However, at volcanoes and regions with topography or obstructions that block the direct path of sound, recent studies have shown that numerical modeling is necessary to provide an accurate source location. A heterogeneous and moving atmosphere (winds) may also affect the location. The time reversal mirror (TRM) application of Kim et al. (2015) back-propagates the wavefield using a Finite Difference Time Domain (FDTD) algorithm, with the source corresponding to the location of peak convergence. Although it provides high-resolution source localization and can account for complex wave propagation, TRM is computationally expensive and limited to individual events. Here we present a new technique, termed RTM-FDTD, which integrates TRM and FDTD. Travel time and transmission loss information is computed from each station to the entire potential source grid from 3-D Green's functions derived via FDTD. The wave energy is then back-projected and stacked at each grid point, with the maximum corresponding to the likely source. We apply our method to detect and characterize thousands of explosions from Yasur Volcano, Vanuatu and Etna Volcano, Italy, which both provide complex wave propagation and multiple source locations. We compare our results with those from more traditional methods (e.g. semblance), and suggest our method is preferred as it is computationally less expensive than TRM but still integrates numerical modeling. RTM-FDTD could be applied to volcanic other anthropogenic sources at a wide variety of ranges and scenarios. Kim, K., Lees, J.M., 2015. Imaging volcanic infrasound sources using time reversal mirror algorithm. Geophysical Journal International 202, 1663-1676.
NASA Astrophysics Data System (ADS)
Sen, Indra S.; Bizimis, Michael; Tripathi, Sachchida Nand; Paul, Debajyoti
2016-03-01
Anthropogenic Pb in the environment is primarily sourced from combustion of fossil fuel and high-temperature industries such as smelters. Identifying the sources and pathways of anthropogenic Pb in the environment is important because Pb toxicity is known to have adverse effects on human health. Pb pollution sources for America, Europe, and China are well documented. However, sources of atmospheric Pb are unknown in India, particularly after leaded gasoline was phased out in 2000. India has a developing economy with a rapidly emerging automobile and high temperature industry, and anthropogenic Pb emission is expected to rise in the next decade. In this study, we report on the Pb-isotope compositions and trace metal ratios of airborne particulates collected in Kanpur, a large city in northern part of India. The study shows that the PM10 aerosols had elevated concentration of Cd, Pb, Zn, As, and Cu in the Kanpur area, however their concentrations are well below the United States Environmental Protection Agency chronic exposure limit. Lead isotopic and trace metal data reveal industrial emission as the plausible source of anthropogenic Pb in the atmosphere in Kanpur. However, Pb isotopic compositions of potential source end-members are required to fully evaluate Pb contamination in India over time. This is the first study that characterizes the isotopic composition of atmospheric Pb in an Indian city after leaded gasoline was phased out by 2000.
Large contribution of natural aerosols to uncertainty in indirect forcing
NASA Astrophysics Data System (ADS)
Carslaw, K. S.; Lee, L. A.; Reddington, C. L.; Pringle, K. J.; Rap, A.; Forster, P. M.; Mann, G. W.; Spracklen, D. V.; Woodhouse, M. T.; Regayre, L. A.; Pierce, J. R.
2013-11-01
The effect of anthropogenic aerosols on cloud droplet concentrations and radiative properties is the source of one of the largest uncertainties in the radiative forcing of climate over the industrial period. This uncertainty affects our ability to estimate how sensitive the climate is to greenhouse gas emissions. Here we perform a sensitivity analysis on a global model to quantify the uncertainty in cloud radiative forcing over the industrial period caused by uncertainties in aerosol emissions and processes. Our results show that 45 per cent of the variance of aerosol forcing since about 1750 arises from uncertainties in natural emissions of volcanic sulphur dioxide, marine dimethylsulphide, biogenic volatile organic carbon, biomass burning and sea spray. Only 34 per cent of the variance is associated with anthropogenic emissions. The results point to the importance of understanding pristine pre-industrial-like environments, with natural aerosols only, and suggest that improved measurements and evaluation of simulated aerosols in polluted present-day conditions will not necessarily result in commensurate reductions in the uncertainty of forcing estimates.
NASA Astrophysics Data System (ADS)
Lin, J.
2011-12-01
Nitrogen oxides (NOx ≡ NO + NO2) are important atmospheric constituents affecting the tropospheric chemistry, surface air quality and climatic forcing. They are emitted both from anthropogenic and from natural (soil, lightning, biomass burning, etc.) sources, which can be estimated inversely from satellite remote sensing of the vertical column densities (VCDs) of nitrogen dioxide (NO2) in the troposphere. Based on VCDs of NO2 retrieved from OMI, a novel approach is developed in this study to separate anthropogenic emissions of NOx from natural sources over East China for 2006. It exploits the fact that anthropogenic and natural emissions vary with seasons with distinctive patterns. The global chemical transport model (CTM) GEOS-Chem is used to establish the relationship between VCDs of NO2 and emissions of NOx for individual sources. Derived soil emissions are compared to results from a newly developed bottom-up approach. Effects of uncertainties in model meteorology and chemistry over China, an important source of errors in the emission inversion, are evaluated systematically for the first time. Meteorological measurements from space and the ground are used to analyze errors in meteorological parameters driving the CTM.
NASA Astrophysics Data System (ADS)
Miko, S.; Koch, G.; Mesić, S.; Šparica-Miko, M.; Šparica, M.; Čepelak, R.; Bačani, A.; Vreča, P.; Dolenec, T.; Bergant, S.
2008-08-01
Due to their balneotherapeutic features, the organic-rich sediments in Makirina Cove are an important source of healing mud. An environmental geochemistry approach using normalization techniques was applied to evaluate the anthropogenic contribution of trace metals to sediments used as healing mud. Sediment geochemistry was found to be associated with land-use change and storm events, as well as with proximity of a road with heavy traffic in the summer months. Local valley topography preferentially channels lithogenic and pollutant transport to the cove. Concentrations and distribution of trace metals indicate lithogenic (Ni, Cr, Co) and anthropogenic (Pb, Cu, Zn and Se) contributions to the sediments. The calculation of enrichment factors indicates a moderate (EFs between 2-3.5) input of anthropogenic Cu and Pb in surficial sediments to a depth of 10 cm. Patients using the Makirina Cove sediments as healing mud could be to some extent exposed to enhanced uptake of metals from anthropogenic sources via dermal contact.
Atmospheric mercury emissions in Australia from anthropogenic, natural and recycled sources
NASA Astrophysics Data System (ADS)
Nelson, Peter F.; Morrison, Anthony L.; Malfroy, Hugh J.; Cope, Martin; Lee, Sunhee; Hibberd, Mark L.; Meyer, C. P. (Mick); McGregor, John
2012-12-01
The United Nations Environment Programme (UNEP) has begun a process of developing a legally binding instrument to manage emissions of mercury from anthropogenic sources. The UNEP Governing Council has concluded that there is sufficient evidence of significant global adverse impacts from mercury to warrant further international action; and that national, regional and global actions should be initiated as soon as possible to identify populations at risk and to reduce human generated releases. This paper describes the development of, and presents results from, a comprehensive, spatially and temporally resolved inventory of atmospheric mercury emissions from the Australian landmass. Results indicate that the best estimate of total anthropogenic emissions of mercury to the atmosphere in 2006 was 15 ± 5 tonnes. Three industrial sectors contribute substantially to Australian anthropogenic emissions: gold smelting (˜50%, essentially from a single site/operation), coal combustion in power plants (˜15%) and alumina production from bauxite (˜12%). A diverse range of other sectors contribute smaller proportions of the emitted mercury, but industrial emissions account for around 90% of total anthropogenic mercury emissions. The other sectors include other industrial sources (mining, smelting, and cement production) and the use of products containing mercury. It is difficult to determine historical trends in mercury emissions given the large uncertainties in the data. Estimates for natural and re-emitted emissions from soil, water, vegetation and fires are made using meteorological models, satellite observations of land cover and soil and vegetation type, fuel loading, fire scars and emission factors which account for the effects of temperature, insolation and other environmental variables. These natural and re-emitted sources comfortably exceed the anthropogenic emissions, and comprise 4-12 tonnes per year from vegetation, 70-210 tonnes per year from soils, and 21-63 tonnes per year from fires.
NASA Astrophysics Data System (ADS)
Yeo, L. K.; Wang, C.
2016-12-01
Water distribution is closely linked to food and energy security. Aerosol emissions affect cloud properties, as well as atmospheric stability, changing the distribution of precipitation. These changes in precipitation causes changes in water availability, affecting food production and energy generation. These impacts are especially important in Southeast Asia, which uses up to 90% of their water supply for irrigation. In addition, the Mekong river, the largest inland fishery in the world, has 30,000MW of hydropower potential in its lower reaches alone. Modelling the impacts of these anthropogenic emission scenarios will allow us to better understand their downstream effects on hydrology, and any potential feedbacks it may have on future aerosol emissions. In the first step, we run the WRF model using FNL reanlaysis data from 2014 and 2015 to generate the WRF-hydro model forcing inputs. We then run the WRF-hydro model and compare the output with current measurements of soil moisture, river flow, and precipitation. Secondly, we run the WRF-Chem model with various anthropogenic emission scenarios and put the results through the WRF-hydro model to determine the impact of these emission scenarios on soil moisture and river flow. The scenarios include enhanced anthropogenic emissions in Asia, anologous to widespread adoption of coal burning as an energy source in Asia. Anthropogenic emissions have the potential to affect energy policy in countries affected by these emissions. When hydropower generation is affected by changes in precipitation, the affected countries will have to switch to alternative sources of fuel to meet their energy needs. These sources typically result in changes in anthropogenic aerosol emisssions, especially if coal is used as an alternative source of energy.
NASA Technical Reports Server (NTRS)
Fisher, J. A.; Jacob, D. J.; Purdy, M. T.; Kopacz, M.; LeSager, P.; Carouge, C.; Holmes, C. D.; Yantosca, R. M.; Batchelor, R. L.; Strong, K.;
2009-01-01
We use aircraft observations of carbon monoxide (CO) from the NASA ARCTAS and NOAA ARCPAC campaigns in April 2008 together with multiyear (2003-2008) CO satellite data from the AIRS instrument and a global chemical transport model (GEOS-Chem) to better understand the sources, transport, and interannual variability of pollution in the Arctic in spring. Model simulation of the aircraft data gives best estimates of CO emissions in April 2008 of 26 Tg month-1 for Asian anthropogenic, 9.1 for European anthropogenic, 4.2 for North American anthropogenic, 9.3 for Russian biomass burning (anomalously large that year), and 21 for Southeast Asian biomass burning. We find that Asian anthropogenic emissions are the dominant source of Arctic CO pollution everywhere except in surface air where European anthropogenic emissions are of similar importance. Synoptic pollution influences in the Arctic free troposphere include contributions of comparable magnitude from Russian biomass burning and from North American, European, and Asian anthropogenic sources. European pollution dominates synoptic variability near the surface. Analysis of two pollution events sampled by the aircraft demonstrates that AIRS is capable of observing pollution transport to the Arctic in the mid-troposphere. The 2003-2008 record of CO from AIRS shows that interannual variability averaged over the Arctic cap is very small. AIRS CO columns over Alaska are highly correlated with the Ocean Nino Index, suggesting a link between El Nino and northward pollution transport. AIRS shows lower-than-average CO columns over Alaska during April 2008, despite the Russian fires, due to a weakened Aleutian Low hindering transport from Asia and associated with the moderate 2007-2008 La Nina. This suggests that Asian pollution influence over the Arctic may be particularly large under strong El Nino conditions.
Quantitative assessment of Pb sources in isotopic mixtures using a Bayesian mixing model.
Longman, Jack; Veres, Daniel; Ersek, Vasile; Phillips, Donald L; Chauvel, Catherine; Tamas, Calin G
2018-04-18
Lead (Pb) isotopes provide valuable insights into the origin of Pb within a sample, typically allowing for reliable fingerprinting of their source. This is useful for a variety of applications, from tracing sources of pollution-related Pb, to the origins of Pb in archaeological artefacts. However, current approaches investigate source proportions via graphical means, or simple mixing models. As such, an approach, which quantitatively assesses source proportions and fingerprints the signature of analysed Pb, especially for larger numbers of sources, would be valuable. Here we use an advanced Bayesian isotope mixing model for three such applications: tracing dust sources in pre-anthropogenic environmental samples, tracking changing ore exploitation during the Roman period, and identifying the source of Pb in a Roman-age mining artefact. These examples indicate this approach can understand changing Pb sources deposited during both pre-anthropogenic times, when natural cycling of Pb dominated, and the Roman period, one marked by significant anthropogenic pollution. Our archaeometric investigation indicates clear input of Pb from Romanian ores previously speculated, but not proven, to have been the Pb source. Our approach can be applied to a range of disciplines, providing a new method for robustly tracing sources of Pb observed within a variety of environments.
Organic-geochemical investigations on soil layers affected by theTohoku-oki tsunami (March 2011)
NASA Astrophysics Data System (ADS)
Reicherter, Klaus; Schwarzbauer, Jan; Jaffe, Bruce; Szczucinski, Witold
2014-05-01
Geochemical investigations on tsunami deposits, in particular palaeotsunamites, have mainly focused on inorganic indicators that have been used to distinguish between terrestrial and marine matter in sedimentary archives. Observable tsunami deposits may also be characterised by organic-geochemical parameters reflecting the mixture and unexpected transport of marine and terrestrial matter. The application of organic substances with indicative properties has so far not been used, although the approach of using specific indicators to determine prehistoric, historic and recent processes and impacts (so-called biomarker and anthropogenic marker approach) already exists. In particular, for recent tsunami deposit the analysis of anthropogenic or even xenobiotic compounds as indicators for assessing the impact of tsunamis has been neglected so far. The Tohoku-oki tsunami in March 2011 showed the huge threat that tsunamis, and subsequent flooding of coastal lowlands, pose to society. The mainly sandy deposits of this mega-tsunami reach more than 4.5 km inland as there were run-up heights of ca. 10 m (wave height). The destruction of infrastructure by wave action and flooding is accompanied by the release of environmental pollutants (e.g. fuels, fats, tarmac, plastics, heavy metals, etc.) contaminating the coastal areas and ocean. To characterize this event in the sedimentary deposits, we analyzed several soil archives from the Bay of Sendai area. Soil layers representing the tsunami deposits have been contrasted with unaffected pre-tsunami samples by means of organic-geochemical analyses based on GC/MS. Natural compounds and their diagenetic transformation products have been tested as marker compounds for monitoring this recent tsunami. The relative composition of fatty acids, n-alkanes, sesquiterpenes and further substances pointed to significant variations before and after the tsunami event. Additionally, anthropogenic marker compounds (such as soil derived pesticides, source specific PAHs, halogenated aromatics from industrial sources) have been detected and quantified. Concentration profiles of distinct terrestrial pollutants revealed shifts either to increasing but for selected compounds also to decreasing contamination levels. Generally, this preliminary study points to the usefulness of organic indicator compounds for characterising the two-dimensional expansion of recent but in particular historic tsunami events as well as its time scales.
Spatial variation in anthropogenic mortality induces a source-sink system in a hunted mesopredator.
Minnie, Liaan; Zalewski, Andrzej; Zalewska, Hanna; Kerley, Graham I H
2018-04-01
Lethal carnivore management is a prevailing strategy to reduce livestock predation. Intensity of lethal management varies according to land-use, where carnivores are more intensively hunted on farms relative to reserves. Variations in hunting intensity may result in the formation of a source-sink system where carnivores disperse from high-density to low-density areas. Few studies quantify dispersal between supposed sources and sinks-a fundamental requirement for source-sink systems. We used the black-backed jackal (Canis mesomelas) as a model to determine if heterogeneous anthropogenic mortality induces a source-sink system. We analysed 12 microsatellite loci from 554 individuals from lightly hunted and previously unhunted reserves, as well as heavily hunted livestock- and game farms. Bayesian genotype assignment showed that jackal populations displayed a hierarchical population structure. We identified two genetically distinct populations at the regional level and nine distinct subpopulations at the local level, with each cluster corresponding to distinct land-use types separated by various dispersal barriers. Migration, estimated using Bayesian multilocus genotyping, between reserves and farms was asymmetric and heterogeneous anthropogenic mortality induced source-sink dynamics via compensatory immigration. Additionally some heavily hunted populations also acted as source populations, exporting individuals to other heavily hunted populations. This indicates that heterogeneous anthropogenic mortality results in the formation of a complex series of interconnected sources and sinks. Thus, lethal management of mesopredators may not be an effective long-term strategy in reducing livestock predation, as dispersal and, more importantly, compensatory immigration may continue to affect population reduction efforts as long as dispersal from other areas persists.
Source characterization of carbon monoxide and ozone over the Northwestern Pacific in summer 2012
NASA Astrophysics Data System (ADS)
Park, Keyhong; Rhee, Tae Siek
2015-06-01
Carbon monoxide (CO) and ozone (O3) were continuously measured in the marine boundary layer of the East Sea, the Northwestern Pacific, and the Bering Sea onboard R/V Araon in the second halves of July and September of 2012, as a part of the SHIpborne Pole-to-Pole Observations (SHIPPO) program. Depending on the characteristics of each section of the cruise track, up to 66 ppbv and 17 ppbv of CO and O3 variability were observed, respectively. The O3/CO ratio suggests that O3 was dominantly produced by photochemical reactions in the troposphere, although in the northern sections of the cruise track, the ratio likely suggests vertical transport from the free troposphere or the lowermost stratosphere. To analyze the source characteristics and the transport of both trace gases, a tagging technique in a 3-D global chemical transport model (Model for OZone And Related chemical Tracers-4; MOZART-4) was applied. The model reproduced the observations fairly well, and the technique enabled us to characterize the source regions and composition of the observed CO. Anthropogenic emissions from Northeastern Asian countries appeared to be substantial sources of the CO in the southern sections, and biomass burning in Siberia was an important source of the CO observed in the northern sections of the cruise track. Long-range transport of anthropogenic CO emissions was distinct over the Bering Sea, where the comparable contributions from North America, Northeast Asia, and Europe were identified. Low CO events driven by southern hemispheric invasion were encountered at the southern coast of the Korean peninsula and in the North Pacific at ∼50N latitude. The model pointed to a noticeable contribution from the open ocean in the Southern Hemisphere for these events.
Removal of sulfur dioxide and formation of sulfate aerosol in Tokyo
NASA Astrophysics Data System (ADS)
Miyakawa, T.; Takegawa, N.; Kondo, Y.
2007-07-01
Ground-based in situ measurements of sulfur dioxide (SO2) and submicron sulfate aerosol (SO42-) together with carbon monoxide (CO) were conducted at an urban site in Tokyo, Japan from spring 2003 to winter 2004. The observed concentrations of SO2 were affected dominantly by anthropogenic emissions (for example, manufacturing industries) in source areas, while small fraction of the data (<30%) was affected by large point sources of SO2 (power plant and volcano). Although emission sources of CO in Tokyo are different from those of SO2, the major emission sources of CO and SO2 are colocated, indicating that CO can be used as a tracer of anthropogenic SO2 emissions in Tokyo. The ratio of SO42- to total sulfur compounds (SOx = SO2 + SO42-) and the remaining fraction of SOx, which is derived as the ratio of the linear regression slope of the SOx-CO correlation, is used as measures for the formation of SO42- and removal of SOx, respectively. Using these parameters, the average formation efficiency of SO42- (i.e., amount of SO42- produced per SO2 emitted from emission sources) are estimated to be 0.18 and 0.03 in the summer and winter periods, respectively. A simple box model was developed to estimate the lifetime of SOx. The lifetime of SOx for the summer period (26 h) is estimated to be about two times longer than that for the winter period (14 h). The seasonal variations of the remaining fraction of SOx, estimated formation efficiency of SO42-, and lifetime of SOx are likely due to those of the boundary layer height and photochemical activity (i.e., hydroxyl radical). These results provide useful insights into the formation and removal processes of sulfur compounds exported from an urban area.
Singer, Michael Bliss; Sargeant, Christopher I; Piégay, Hervé; Riquier, Jérémie; Wilson, Rob J S; Evans, Cristina M
2014-01-01
Seasonal and annual partitioning of water within river floodplains has important implications for ecohydrologic links between the water cycle and tree growth. Climatic and hydrologic shifts alter water distribution between floodplain storage reservoirs (e.g., vadose, phreatic), affecting water availability to tree roots. Water partitioning is also dependent on the physical conditions that control tree rooting depth (e.g., gravel layers that impede root growth), the sources of contributing water, the rate of water drainage, and water residence times within particular storage reservoirs. We employ instrumental climate records alongside oxygen isotopes within tree rings and regional source waters, as well as topographic data and soil depth measurements, to infer the water sources used over several decades by two co-occurring tree species within a riparian floodplain along the Rhône River in France. We find that water partitioning to riparian trees is influenced by annual (wet versus dry years) and seasonal (spring snowmelt versus spring rainfall) fluctuations in climate. This influence depends strongly on local (tree level) conditions including floodplain surface elevation and subsurface gravel layer elevation. The latter represents the upper limit of the phreatic zone and therefore controls access to shallow groundwater. The difference between them, the thickness of the vadose zone, controls total soil moisture retention capacity. These factors thus modulate the climatic influence on tree ring isotopes. Additionally, we identified growth signatures and tree ring isotope changes associated with recent restoration of minimum streamflows in the Rhône, which made new phreatic water sources available to some trees in otherwise dry years. Key Points Water shifts due to climatic fluctuations between floodplain storage reservoirs Anthropogenic changes to hydrology directly impact water available to trees Ecohydrologic approaches to integration of hydrology afford new possibilities PMID:25506099
Banks, William S.L.; Reyes, Betzaida
2009-01-01
A source- and finished-water-quality assessment of groundwater was conducted in the Piedmont Physiographic Province of Maryland and Virginia in the Potomac River Basin during 2003-04 as part of the U.S. Geological Survey's National Water-Quality Assessment Program. This assessment used a two-phased approach to sampling that allowed investigators to evaluate the occurrence of more than 280 anthropogenic organic compounds (volatile organic compounds, pesticides and pesticide degradates, and other anthropogenic organic compounds). Analysis of waters from 15 of the largest community water systems in the study area were included in the assessment. Source-water samples (raw-water samples collected prior to treatment) were collected at the well head. Finished-water samples (raw water that had been treated and disinfected) were collected after treatment and prior to distribution. Phase one samples, collected in August and September 2003, focused on source water. Phase two analyzed both source and finished water, and samples were collected in August and October of 2004. The results from phase one showed that samples collected from the source water for 15 community water systems contained 92 anthropogenic organic compounds (41 volatile organic compounds, 37 pesticides and pesticide degradates, and 14 other anthropogenic organic compounds). The 5 most frequently occurring anthropogenic organic compounds were detected in 11 of the 15 source-water samples. Deethylatrazine, a degradate of atrazine, was present in all 15 samples and metolachlor ethanesulfonic acid, a degradate of metolachlor, and chloroform were present in 13 samples. Atrazine and metolachlor were present in 12 and 11 samples, respectively. All samples contained a mixture of compounds with an average of about 14 compounds per sample. Phase two sampling focused on 10 of the 15 community water systems that were selected for resampling on the basis of occurrence of anthropogenic organic compounds detected most frequently during the first phase. A total of 48 different anthropogenic organic compounds were detected in samples collected from source and finished water. There were a similar number of compounds detected in finished water (41) and in source water (39). The most commonly detected group of anthropogenic organic compounds in finished water was trihalomethanes - compounds associated with the disinfection of drinking water. This group of compounds accounted for 30 percent of the detections in source water and 44 percent of the detections in finished water, and were generally found in higher concentrations in finished water. Excluding trihalomethanes, the number of total detections was about the same in source-water samples (33) as it was in finished-water samples (35). During both phases of the study, two measurements for human-health assessment were used. The first, the Maximum Contaminant Level for drinking water, is set by the U.S. Environmental Protection Agency and represents a legally enforceable maximum concentration of a contaminant permitted in drinking water. The second, the Health-Based Screening Level, was developed by the U.S. Geological Survey, is not legally enforceable, and represents a limit for more chronic exposures. Maximum concentrations for each detected compound were compared with either the Maximum Contaminant Level or the Health-Based Screening Level when available. More than half of the compounds detected had either a Maximum Contaminant Level or a Health-Based Screening Level. A benchmark quotient was set at 10 percent (greater than or equal to 0.1) of the ratio of the detected concentration of a particular compound to its Maximum Contaminant Level, or Health-Based Screening Level. This was considered a threshold for further monitoring. During phase one, when only source water was sampled, seven compounds (chloroform, benzene, acrylonitrile, methylene chloride, atrazine, alachlor, and dieldrin) met or exceeded a benchmark quotient. No de
NASA Astrophysics Data System (ADS)
Lin, J.-T.
2012-04-01
Nitrogen oxides (NOx ≡ NO + NO2) are important atmospheric constituents affecting the tropospheric chemistry and climate. They are emitted both from anthropogenic and from natural (soil, lightning, biomass burning, etc.) sources, and China has become a major region of increasing importance for anthropogenic sources. In a series of studies, satellite remote sensing for the vertical column densities (VCDs) of tropospheric nitrogen dioxide (NO2) is used to estimate anthropogenic and natural emissions of NOx over China. Focus is set on variations of emissions over a variety of time scales in response to the economic development of China, from the general growth in recent years to the economic downturn during late 2008 - mid 2009 to the holiday associated with the Chinese New Year. An attempt is made to reduce the effect of potential systematic errors in satellite retrievals by coupling data from multiple satellite instruments flying over China at different time of day. For 2006, anthropogenic emissions are separated from lightning and soil sources over East China by exploiting their different seasonality. For the first time, a systematic evaluation is conducted to quantify uncertainties in various aspects of model meteorology and chemistry affecting emission inversion for China and implications for simulations of other air pollution (e.g., near-surface ozone).
Re, V; Sacchi, E; Mas-Pla, J; Menció, A; El Amrani, N
2014-12-01
Groundwater pollution from anthropogenic sources is a serious concern affecting several coastal aquifers worldwide. Increasing groundwater exploitation, coupled with point and non-point pollution sources, are the main anthropogenic impacts on coastal environments and are responsible for severe health and food security issues. Adequate management strategies to protect groundwater from contamination and overexploitation are of paramount importance, especially in arid prone regions, where coastal aquifers often represent the main freshwater resource to sustain human needs. The Bou-Areg Aquifer (Morocco) is a perfect example of a coastal aquifer constantly exposed to all the negative externalities associated with groundwater use for agricultural purposes, which lead to a general increase in aquifer salinization. In this study data on 61 water samples, collected in June and November 2010, were used to: (i) track groundwater composition changes related to the use of irrigation water from different sources, (ii) highlight seasonal variations to assess aquifer vulnerability, and (iii) present a reproducible example of multi-tracer approach for groundwater management in rural coastal areas. Hydrogeochemical results show that Bou-Areg groundwater is characterized by - high salinity, associated with a remarkable increase in bicarbonate content in the crop growing season, due to more intense biological activity in irrigated soils. The coupled multi-tracer and statistical analysis confirms the strong dependency on irrigation activities as well as a clear identification of the processes governing the aquifer's hydrochemistry in the different seasons. Water Rock Interaction (WRI) dominates the composition of most of groundwater samples in the Low Irrigation season (L-IR) and Agricultural Return Flow (ARF) mainly affects groundwater salinization in the High Irrigation season (H-IR) in the same areas naturally affected by WRI. In the central part of the plain River Recharge (RR) from the Selouane River is responsible for the high groundwater salinity whilst Mixing Processes (MIX) occur in absence of irrigation activities. Copyright © 2014 Elsevier B.V. All rights reserved.
Franzen-Klein, Dana; McRuer, David; Slabe, Vincent; Katzner, Todd
2018-01-01
A male juvenile bald eagle (Haliaeetus leucocephalus) was admitted to the Wildlife Center of Virginia with a left humeral fracture a large quantity of anthropogenic debris in the ventriculus, a blood lead level of 0.616 ppm, and clinical signs consistent with chronic lead toxicosis. Because of the poor prognosis for recovery and release, the eagle was euthanatized. Lead isotope analysis was performed to identify potential anthropogenic sources of lead in this bird. The lead isotope ratios in the eagle's femur (0.8773), liver (0.8761), and kidneys (0.8686) were most closely related to lead paint (0.8925), leaded gasoline (0.8450), and zinc smelting (0.8240). The lead isotope ratios were dissimilar to lead ammunition (0.8179) and the anthropogenic debris in the ventriculus. This case report documents foreign body ingestion in a free-ranging bald eagle and demonstrates the clinical utility of lead isotope analysis to potentially identify or exclude anthropogenic sources of lead poisoning in wildlife patients.
NASA Astrophysics Data System (ADS)
Ivošević, T.; Orlić, I.; Bogdanović Radović, I.; Čargonja, M.; Stelcer, E.
2017-09-01
In the city of Rijeka, Croatia, an extended, two-year aerosol pollution monitoring campaign was recently completed. During that period, 345 samples of fine fraction of aerosols were collected on stretched Teflon filters. All samples were analyzed by Ion Beam Analysis techniques Proton Induced X-ray Emission and Proton Induced γ-Ray Emission and concentrations of 22 elements were determined. Concentrations of black carbon were determined by Laser Integrated Plate Method. For the Bay of Kvarner, where the city of Rijeka is located, long periods of calm weather are common. As a consequence, during these periods, air pollution is steadily increasing. To pin-point and characterize local, mostly anthropogenic, air pollution sources, only samples collected during the extended calm periods were used in this work. As a cut-off wind speed, speed of 1.5 m/s was used. In that way, out of all 345 samples, only 188 were selected. Those samples were statistically evaluated by means of positive matrix factorization. Results show that from all anthropogenic sources (vehicles, secondary sulphates, smoke, heavy oil combustion, road dust, industry Fe and port activities) only secondary sulphates and heavy oil combustion were significantly higher (40% and 50%, respectively) during calm periods. On the other hand, natural components of aerosol pollution such as soil and sea salts, (typically present in concentrations of 1.4% and 9%, respectively) are practically non-existent for calm weather conditions.
Effects of Nitrogen Inputs and Watershed Characteristics on ...
Nitrogen (N) inputs to the landscape have been linked previously to N loads exported from watersheds at the national scale; however, stream N concentration is arguably more relevant than N load for drinking water quality, freshwater biological responses and establishment of nutrient criteria. In this study, we combine national-scale anthropogenic N input data, including synthetic fertilizer, crop biological N fixation, manure applied to farmland, atmospheric N deposition, and point source inputs, with data from the 2008-09 National Rivers and Streams Assessment to quantify the relationship between N inputs and in-stream concentrations of total N (TN), dissolved inorganic N (DIN), and total organic N (TON) (calculated as TN – DIN). In conjunction with simple linear regression, we use multiple regression to understand how watershed and stream reach attributes modify the effect of N inputs on N concentrations. Median TN was 0.50 mg N L-1 with a maximum of 25.8 mg N L-1. Total N inputs to the watershed ranged from less than 1 to 196 kg N ha-1 y-1, with a median of 14.4 kg N ha-1 y-1. Atmospheric N deposition was the single largest anthropogenic N source in the majority of sites, but, agricultural sources generally dominate total N inputs in sites with elevated N concentrations. The sum of all N inputs were positively correlated with concentrations of all forms of N [r2 = 0.44, 0.43, and 0.18 for TN, DIN, and TON, respectively (all log-transformed), n = 1112], indi
Accumulation of atmospheric radionuclides and heavy metals in cryoconite holes on an Arctic glacier.
Łokas, Edyta; Zaborska, Agata; Kolicka, Małgorzata; Różycki, Michał; Zawierucha, Krzysztof
2016-10-01
Surface of glaciers is covered by mineral and organic dust, together with microorganisms forming cryoconite granules. Despite fact that glaciers and ice sheets constitute significance part of land surface, reservoir of freshwater, and sites of high biological production, the knowledge on the cryoconite granules still remain unsatisfactory. This study presents information on radionuclide and heavy metal contents in cryoconites. Cryoconites collected from the Hans Glacier in SW Spitsbergen reveal high activity concentrations of anthropogenic ((238,239,240)Pu, (137)Cs, (90)Sr) and natural ((210)Pb) radionuclides. The (238)Pu/(239+240)Pu activity ratios in these cryoconites significantly exceed the mean global fallout ratio (0.025). The (238)Pu/(239+240)Pu ranged from 0.064 to 0.118. The (239+240)Pu/(137)Cs varied from 0.011 ± 0.003 to 0.030 ± 0.007. Such activity ratios as observed in these cryoconites were significantly higher than the values characterizing global fallout, pointing to possible contributions of these radionuclides from other sources. Heavy metals (Pb, Cd, Cu, Zn, Fe, and Mn) in cryoconites exceed both UCC concentrations and local rocks' concentrations, particularly for cadmium. The concentration ratios of stable lead isotopes ((206)Pb/(207)Pb, (208)Pb/(206)Pb) were determined to discriminate between the natural and anthropogenic sources of Pb in cryoconites and to confirm the strong anthropogenic contribution to heavy metal deposition in the Arctic. In investigated cryoconite holes, two groups of invertebrates, both extremophiles, Tardigrada and Rotifera were detected. Our study indicate that cryoconites are aggregates of mineral and organic substances on surfaces of glaciers are able to accumulate large amounts of airborne pollutants bound to extracellular polymeric substances secreted by microorganisms. Copyright © 2016 Elsevier Ltd. All rights reserved.
Paulot, Fabien; Jacob, Daniel J; Henze, Daven K
2013-04-02
Anthropogenic enrichment of reactive nitrogen (Nr) deposition is an ecological concern. We use the adjoint of a global 3-D chemical transport model (GEOS-Chem) to identify the sources and processes that control Nr deposition to an ensemble of biodiversity hotspots worldwide and two U.S. national parks (Cuyahoga and Rocky Mountain). We find that anthropogenic sources dominate deposition at all continental sites and are mainly regional (less than 1000 km) in origin. In Hawaii, Nr supply is controlled by oceanic emissions of ammonia (50%) and anthropogenic sources (50%), with important contributions from Asia and North America. Nr deposition is also sensitive in complicated ways to emissions of SO2, which affect Nr gas-aerosol partitioning, and of volatile organic compounds (VOCs), which affect oxidant concentrations and produce organic nitrate reservoirs. For example, VOC emissions generally inhibit deposition of locally emitted NOx but significantly increase Nr deposition downwind. However, in polluted boreal regions, anthropogenic VOC emissions can promote Nr deposition in winter. Uncertainties in chemical rate constants for OH + NO2 and NO2 hydrolysis also complicate the determination of source-receptor relationships for polluted sites in winter. Application of our adjoint sensitivities to the representative concentration pathways (RCPs) scenarios for 2010-2050 indicates that future decreases in Nr deposition due to NOx emission controls will be offset by concurrent increases in ammonia emissions from agriculture.
Anthropogenic aerosols as a source of ancient dissolved organic matter in glaciers
Stubbins, Aron; Hood, Eran; Raymond, Peter A.; Aiken, George R.; Sleighter, Rachel L.; Hernes, Peter J.; Butman, David; Hatcher, Patrick G.; Striegl, Robert G.; Schuster, Paul F.; Abdulla, Hussain A.N.; Vermilyea, Andrew W.; Scott, Durelle T.; Spencer, Robert G.M.
2012-01-01
Glacier-derived dissolved organic matter represents a quantitatively significant source of ancient, yet highly bioavailable carbon to downstream ecosystems. This finding runs counter to logical perceptions of age–reactivity relationships, in which the least reactive material withstands degradation the longest and is therefore the oldest. The remnants of ancient peatlands and forests overrun by glaciers have been invoked as the source of this organic matter. Here, we examine the radiocarbon age and chemical composition of dissolved organic matter in snow, glacier surface water, ice and glacier outflow samples from Alaska to determine the origin of the organic matter. Low levels of compounds derived from vascular plants indicate that the organic matter does not originate from forests or peatlands. Instead, we show that the organic matter on the surface of the glaciers is radiocarbon depleted, consistent with an anthropogenic aerosol source. Fluorescence spectrophotometry measurements reveal the presence of protein-like compounds of microbial or aerosol origin. In addition, ultrahigh-resolution mass spectrometry measurements document the presence of combustion products found in anthropogenic aerosols. Based on the presence of these compounds, we suggest that aerosols derived from fossil fuel burning are a source of pre-aged organic matter to glacier surfaces. Furthermore, we show that the molecular signature of the organic matter is conserved in snow, glacier water and outflow, suggesting that the anthropogenic carbon is exported relatively unchanged in glacier outflows.
Estimation of global anthropogenic dust aerosol using CALIOP satellite
NASA Astrophysics Data System (ADS)
Chen, B.; Huang, J.; Liu, J.
2014-12-01
Anthropogenic dust aerosols are those produced by human activity, which mainly come from cropland, pasture, and urban in this paper. Because understanding of the emissions of anthropogenic dust is still very limited, a new technique for separating anthropogenic dust from natural dustusing CALIPSO dust and planetary boundary layer height retrievalsalong with a land use dataset is introduced. Using this technique, the global distribution of dust is analyzed and the relative contribution of anthropogenic and natural dust sources to regional and global emissions are estimated. Local anthropogenic dust aerosol due to human activity, such as agriculture, industrial activity, transportation, and overgrazing, accounts for about 22.3% of the global continentaldust load. Of these anthropogenic dust aerosols, more than 52.5% come from semi-arid and semi-wet regions. On the whole, anthropogenic dust emissions from East China and India are higher than other regions.
Asian anthropogenic dust and its climate effect (Invited)
NASA Astrophysics Data System (ADS)
Huang, J.; Liu, J.; Chen, B.
2013-12-01
Anthropogenic dust originates mainly from areas of localized human disturbance, such as traffic-on-roads, agricultural fields, grazing, military installations, construction sites, and off-road vehicle areas. To understand historical and possible future changes in dust emissions, the percentage of atmospheric dust load originating from anthropogenic source and its distribution must be quantified. CALIPSO lidar, which shoots a laser into the atmosphere, provides new insight into the detection of anthropogenic dust emission. Here, we present the distribution of Asian anthropogenic dust emissions and its relation to human activity by using CALIPSO lidar measurements. We found that the local anthropogenic dust aerosols account for significant portion of the total dust burden in the atmosphere. The anthropogenic dust emissions mainly occur over the heavy human activity and poor ecosystem region, such as semi-arid region. The impact of Asian anthropogenic dust on regional climate will also be discussed in this talk.
EMISSIONS OF ORGANIC AIR TOXICS FROM OPEN ...
A detailed literature search was performed to collect and collate available data reporting emissions of toxic organic substances into the air from open burning sources. Availability of data varied according to the source and the class of air toxics of interest. Volatile organic compound (VOC) and polycyclic aromatic hydrocarbon (PAH) data were available for many of the sources. Data on semivolatile organic compounds (SVOCs) that are not PAHs were available for several sources. Carbonyl and polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofuran (PCDD/F) data were available for only a few sources. There were several sources for which no emissions data were available at all. Several observations were made including: 1) Biomass open burning sources typically emitted less VOCs than open burning sources with anthropogenic fuels on a mass emitted per mass burned basis, particularly those where polymers were concerned; 2) Biomass open burning sources typically emitted less SVOCs and PAHs than anthropogenic sources on a mass emitted per mass burned basis. Burning pools of crude oil and diesel fuel produced significant amounts of PAHs relative to other types of open burning. PAH emissions were highest when combustion of polymers was taking place; and 3) Based on very limited data, biomass open burning sources typically produced higher levels of carbonyls than anthropogenic sources on a mass emitted per mass burned basis, probably due to oxygenated structures r
NASA Astrophysics Data System (ADS)
ul-Haq, Zia; Tariq, Salman; Ali, Muhammad
2015-12-01
In the present work we have studied spatial and temporal variability of methane total column (MTC) over Pakistan and neighboring regions of Afghanistan, India and Iran by using observations of SCanning Imaging Absorption SpectroMeter for Atmospheric CHartographY (SCIAMACHY) aboard EOS ENVISAT. Satellite measurements show large spatio-temporal variations in MTC over the study domain at different time scales. We find an average MTC of 1787±22 ppb (annual average±standard deviation) with 3.7% (slope 7.14±1.28, y-intercept 1751±7.19, r=0.91) increase during the period of January 2003 to April 2012. An enhanced MTC is observed mostly over the Indo-Gangetic Plain and areas with high anthropogenic activities. MTC exhibits a seasonal peak of 1804±28 ppb in summer followed by autumn (1800±25 ppb) and winter (1777±24 ppb). We have also discussed anthropogenic emission estimates in the study area obtained from EDGAR database. Substantial increments of 77% and 61% are observed in anthropogenic CH4 emissions for Pakistan and Afghanistan, respectively, during 1990-2008. Anthropogenic CH4 emissions from enteric fermentation and livestock sectors are found to be the highest. EDGAR data have also identified megacity Lahore, Sukkur, megacity Karachi, Dera Ghazi Khan, megacity Delhi and Ahmedabad as large point sources of CH4 emissions in the region. The emissions from Karachi show the highest increase of 107%, while Lahore is found with the highest annual average emissions of 8.8×10-10 kg m-2 s-1.
BIOINDICATORS OF SUSTAINABLE DEVELOPMENT STRATEGIES IN SUBTROPICAL CLIMATES
Anthropogenic sediment and nutrients inputs to aquatic systems associated with urbanization are commonly cited as threatening water quality and ultimately overall ecosystem stability and productivity. Although anthropogenic nutrient sources are rarely detected as elevated diss...
GLOBAL INVENTORY OF VOLATILE COMPOUND EMISSIONS FROM ANTHROPOGENIC SOURCES
The report describes a global inventory anthropogenic volatile organic compound (VOC) emissions that includes a separate inventory for each of seven pollutant groups--paraffins, olefins, aromatics, formaldehyde, other aldehydes, other aromatics, and marginally reactive compounds....
Schmale, Julia; Flanner, Mark; Kang, Shichang; Sprenger, Michael; Zhang, Qianggong; Guo, Junming; Li, Yang; Schwikowski, Margit; Farinotti, Daniel
2017-01-01
Deposited mineral dust and black carbon are known to reduce the albedo of snow and enhance melt. Here we estimate the contribution of anthropogenic black carbon (BC) to snowmelt in glacier accumulation zones of Central Asia based on in-situ measurements and modelling. Source apportionment suggests that more than 94% of the BC is emitted from mostly regional anthropogenic sources while the remaining contribution comes from natural biomass burning. Even though the annual deposition flux of mineral dust can be up to 20 times higher than that of BC, we find that anthropogenic BC causes the majority (60% on average) of snow darkening. This leads to summer snowmelt rate increases of up to 6.3% (7 cm a−1) on glaciers in three different mountain environments in Kyrgyzstan, based on albedo reduction and snowmelt models. PMID:28079148
NASA Astrophysics Data System (ADS)
El-Sorogy, Abdelbaset S.; Youssef, Mohamed; Al-Kahtany, Khaled; Al-Otaiby, Naif
2016-01-01
In order to assess arsenic on the Tarut coast, Saudi Arabian Gulf, 38 sediment samples, 26 seawater samples and 40 gastropod and bivalve specimens were collected for analyses by Inductively Coupled Plasma-Mass Spectrometer. The Enrichment Factor (EF), the Geoaccumulation Index (Igeo) and the Contamination Factor (CF) indicated that coastal sediments of Tarut Island are severely enriched, strongly polluted and very highly contaminated with arsenic as a result of anthropogenic inputs. Comparison with arsenic in coastal sediments, seawaters and molluscs in the Red Sea, the Arabian Gulf and abroad coasts suggested that the studied samples have higher concentrations of As. The suggested natural sources of arsenic in the study area are the weathering and decomposition of neighboring deserts. The anthropogenic sources include the land reclamation, petrochemical industries, boat exhaust emissions, oil leakage, desalination plants and sewage effluents. These anthropogenic sources are the dominant sources of As in the study area and mostly came from Al Jubail industrial city to the north.
Assessment of global industrial-age anthropogenic arsenic contamination.
Han, Fengxiang X; Su, Yi; Monts, David L; Plodinec, M John; Banin, Amos; Triplett, Glover E
2003-09-01
Arsenic, a carcinogenic trace element, threatens not only the health of millions of humans and other living organisms, but also global sustainability. We present here, for the first time, the global industrial-age cumulative anthropogenic arsenic production and its potential accumulation and risks in the environment. In 2000, the world cumulative industrial-age anthropogenic arsenic production was 4.53 million tonnes. The world-wide coal and petroleum industries accounted for 46% of global annual gross arsenic production, and their overall contribution to industrial-age gross arsenic production was 27% in 2000. Global industrial-age anthropogenic As sources (as As cumulative production) follow the order: As mining production>As generated from coal>As generated from petroleum. The potential industrial-age anthropogenic arsenic input in world arable surface in 2000 was 2.18 mg arsenic kg(-1), which is 1.2 times that in the lithosphere. The development of substitute materials for arsenic applications in the agricultural and forestry industries and controls of arsenic emissions from the coal industry may be possible strategies to significantly decrease arsenic pollution sources and dissipation rates into the environment.
NASA Astrophysics Data System (ADS)
Uglietti, C.; Gabrielli, P.; Thompson, L. G.
2013-12-01
The recent increase in trace element concentrations, for example Cr, Cu, Zn, Ag, Pb, Bi, and U, in polar snow and ice has provided compelling evidence of a hemispheric change in atmospheric composition since the nineteenth century. This change has been concomitant with the expansion of the Industrial Revolution and points towards an anthropogenic source of trace elements in the atmosphere. There are very few low latitude trace element ice core records and these are believed to be sensitive to perturbations of regional significance. To date, these records have not been used to document a preindustrial anthropogenic impact on atmospheric composition at low latitudes. Ice cores retrieved from the tropical Andes are particularly interesting because they have the potential to reveal detailed information about the evolution and environmental consequences of mineral exploitation related to the Pre Inca Civilizations, the Inca Empire (1438-1533 AD) and the subsequent Spanish invasion and dominance (1532-1833 AD). The chemical record preserved in the ice of the Quelccaya ice cap (southern Peruvian Andes) offers the exceptional opportunity to geochemically constrain the composition of the tropical atmosphere at high resolution over the last ~1200 years. Quantification of twenty trace elements (Ag, Al, As, Bi, Cd, Co, Cr, Cu, Fe, Mn, Mo, Pb, Rb, Sb, Sn, Ti, Tl, U, V, and Zn) was performed by ICP-SFMS over 105 m of the Quelccaya North Dome core (5600 m asl, 128.57 m) by analyzing 2450 samples. This provides the first atmospheric trace element record in South America spanning continuously and at high resolution for the time period between 1990 and 790 AD. Ag, As, Bi, Cd, Cr, Co, Cu, Mn, Mo, Sb, Sn, Pb and Zn show increases in concentration and crustal enrichment factor starting at different times between 1450 and 1550 AD, in concomitance with the expansions of the Inca Empire and, subsequently, the Spanish Empire well before the inception of the Industrial Revolution. This indicates that there have been additional anthropogenic sources that have impacted the South American atmosphere during the past ~550 years. Furthermore, As, Bi and Pb record shows, the two most significant increases have occurred in the 20th century, one beginning in ~1905 AD and peaking in the 1920s and the second beginning in ~1955 AD and peaking in the 1970s. Comparison with other trace element records from Greenland and Antarctica reveals concomitant peaks of different amplitude in Pb concentration and crustal enrichment factor, possibly pointing to an unexpected larger than regional scale significance for the Quelccaya ice core record during the last century. In conclusion, the Quelccaya ice core indicates that societal and industrial development influenced the atmospheric composition in South America, from different large scale sources, during the last ~550 years. This is the first time that a low latitude ice core record has been used to reconstruct pre-industrial anthropogenic forcing on the atmosphere.
NASA Astrophysics Data System (ADS)
Linhoff, B.; Norton, S.; Travis, R.; Romero, Z.; Waters, B.
2017-12-01
Nitrate contamination of groundwater is a major problem globally including within the Albuquerque Basin in New Mexico. Ingesting high concentrations of nitrate (> 10 mg/L as N) can lead to an increased risk of cancer and to methemoglobinemia in infants. Numerous anthropogenic sources of nitrate have been identified within the Albuquerque Basin including fertilizers, landfills, multiple sewer pipe releases, sewer lagoons, domestic septic leach fields, and a nitric acid line outfall. Furthermore, groundwater near ephemeral streams often exhibits elevated NO3 concentrations and high NO3/Cl ratios incongruous with an anthropogenic source. These results suggest that NO3 can be concentrated through evaporation beneath ephemeral streams and mobilized via irrigation or land use change. This study seeks to use extensive geochemical analyses of groundwater and surface water to differentiate between various sources of NO3 contamination. The U.S. Geological Survey collected 54 groundwater samples from wells and six samples from ephemeral streams from within and from outside of areas of known nitrate contamination. To fingerprint the sources of nitrate pollution, samples were analyzed for major ions, trace metals, nutrients, dissolved gases, δ15N and δ18O in NO3, δ15N within N2 gas, and, δ2H and δ18O in H2O. Furthermore, most sites were sampled for artificial sweeteners and numerous contaminants of emerging concern including pharmaceutical drugs, caffeine, and wastewater indicators. This study will also investigate the age distribution of groundwater and the approximate age of anthropogenic NO3 contamination using 3He/4He, δ13C, 14C, 3H, as well as pharmaceutical drugs and artificial sweeteners with known patent and U.S. Food and Drug Administration approval dates. This broad suite of analytes will be used to differentiate between naturally occurring and multiple anthropogenic NO3 sources, and to potentially determine the approximate date of NO3 contamination.
Complex anthropogenic sources of platinum group elements in aerosols on Cape Cod, USA.
Sen, Indra S; Peucker-Ehrenbrink, Bernhard; Geboy, Nicholas
2013-09-17
Platinum group elements (PGE) of anthropogenic origin have been reported in rainwater, snow, roadside soil and vegetation, industrial waste, and urban airborne particles around the world. As recent studies have shown that PGE are bioavailable in the environment and pose health risks at chronic levels, the extent of PGE pollution is of global concern. In this study, we report PGE concentrations and osmium isotope ((187)Os/(188)Os) ratios of airborne particles (particulate matter, PM10) collected in Woods Hole, a small coastal village on Cape Cod, Massachusetts, U.S.A. The sampling site is more than 100 km away from the nearest urban centers (Boston, Providence) and has no large industrial emission center within a 30 km radius. The study reveals that, although PGE concentrations in rural airborne particulate matter are orders of magnitude lower than in urban aerosols, 69% of the total osmium is of anthropogenic origin. Anthropogenic PGE signatures in airborne particles are thus not restricted to large cities with high traffic flows and substantial industries; they can also be found in rural environments. We further conclude that the combination of Pt/Rh concentration ratios and (187)Os/(188)Os composition can be used to trace PGE sources. The Pt/Rh and (187)Os/(188)Os composition of Woods Hole aerosols indicate that the anthropogenic PGE fraction is primarily sourced from ore smelting processes, with possible minor contributions from fossil fuel burning and automobile catalyst-derived materials. Our results further substantiate the use of (187)Os/(188)Os in source apportionment studies on continental scales.
New discoveries enabled by OMI SO2 measurements and future missions
NASA Astrophysics Data System (ADS)
Krotkov, Nickolay
2010-05-01
The Ozone Monitoring Instrument (OMI) on NASA Aura satellite makes global daily measurements of the total column of sulfur dioxide (SO2), a short-lived trace gas produced by fossil fuel combustion, smelting, and volcanoes. This talk highlights most recent science results enabled by using OMI SO2 data. OMI daily contiguous volcanic SO2 data continue 25+ climatic record by its predecessors (Total Ozone mapping Spectrometers 1978-2005), but higher SO2 sensitivity allows measuring volcanic plumes for a longer time as well as measuring passive volcanic degassing from space. New algorithm development allows direct estimating of SO2 plume heights to refine SO2 tonnages in largest volcanic plumes important for climate applications. Quantitatively, anthropogenic SO2 is more difficult to measure from space, since ozone absorption and Rayleigh scattering reduce sensitivity to pollutants in the lower troposphere. OMI data first enabled daily detection of SO2 burdens from individual smelters as well as observed SO2 pollution lofting from boundary layer and long-range transport in free troposphere. Interplay between volcanic and anthropogenic SO2 emissions resulted in highly variable SO2 pollution levels in Peru and Mexico City. We have updated our copper smelter analysis, which showed interesting new trends. Combining OMI data with trajectory models and aerosol/cloud measurements by A-train sensors (MODIS, CALIPSO) allowed tracking long-range transport of volcanic and anthropogenic aerosol/SO2 plumes. These studies placed new constraints on conversion rates of SO2 to sulfate at different heights from free troposphere to the lower stratosphere. We describe new techniques for spatial and time averaging that have been used to determine the global distribution of anthropogenic SO2 burdens, and the efficacy of abatement strategies. OMI seasonal to multi-year average images clearly show the world-highest consistent SO2 pollution in eastern China, mostly due to the burning of high-sulfur coal in its many coal-fired power plants. Recently, China's government has instituted nationwide measures to control SO2 emissions through the adoption of flue-gas desulfurization technology (FGD) on new power plants; and even greater measures were adopted in the Beijing area in anticipation of the Olympic Games. We demonstrate that the OMI can pick up both SO2 and NO2 emissions from large point sources in northern China, where large increases in both gases were observed from 2005 to 2007, over areas with newly established power plants. The OMI SO2/NO2 ratio generally agrees with the estimated emission factors for coal-fired power plants based on a bottom-up approach. Between 2007 and 2008, OMI detected little change in NO2 but dramatic decline in SO2 over the same areas. While the almost constant NO2 levels between the two years imply steady electricity generation from the power plants, the large reduction in SO2 confirms the effectiveness of the FGD units, which likely became operational between 2007 and 2008. Further development of satellite detection and monitoring of point pollution sources requires better than 10km ground resolution. We show how planned Dutch /ESA TROPOMI and NASA GEOCape missions will advance the art of measuring point source emissions in coming decade.
NASA Astrophysics Data System (ADS)
Shiel, Alyssa E.; Weis, Dominique; Orians, Kristin J.
2012-01-01
Environmental monitoring and remediation require techniques to identify the source and fate of metals emissions. The measurement of heavy metal isotopic signatures, made possible by the advent of the MC-ICP-MS, is a powerful new geochemical tool, which may be used to trace the source of these metals in the environment. In a multi-tracer study, Cd, Zn and Pb isotopic compositions (MC-ICP-MS) and elemental concentrations (HR-ICP-MS) are used to distinguish between natural and anthropogenic sources of these metals in bivalves collected from western Canada (British Columbia), Hawaii, and the USA East Coast. Variability in the δ 114/110Cd values of bivalves (-1.20‰ to -0.09‰) is attributed to differences in the relative contributions of Cd from natural and anthropogenic sources between sites. Cadmium isotopic compositions (δ 114/110Cd = -0.69‰ to -0.09‰) identify high Cd levels in B.C. oysters as primarily natural (i.e., upwelling of Cd rich intermediate waters in the North Pacific), with some variability attributed to anthropogenic sources (e.g., mining and smelting). Variability in the δ 66/64Zn values exhibited by the B.C. bivalves is relatively small (0.28-0.36‰). Despite the low Pb levels found in B.C. oysters, Pb isotopes are used to identify emissions from industrial processes and the consumption of unleaded gasoline and diesel fuel as significant metal sources. Although the Cd concentrations of the USA East Coast bivalves are primarily lower than those of B.C. oysters, their relatively light Cd isotopic compositions (δ 114/110Cd = -1.20‰ to -0.54‰) indicate the significance of anthropogenic Cd sources and are attributed to the high prevalence of industry on this coast. The δ 114/110Cd values of USA East Coast bivalves include the lightest ever reported, with the exception of values reported for extraterrestrial materials. In addition, the Pb isotopic compositions of bivalves from the USA East Coast indicate Pb emissions from the combustion of coal are an important source of Pb, consistent with the high consumption of coal for power production on this coast. This study demonstrates the effective use of Cd and Zn isotopes to trace anthropogenic sources in the environment and the benefit of combining these tools with Pb "fingerprinting" techniques.
We used growth rates of juvenile winter flounder Pseudopleuronectes americanus to assess anthropogenic influence on habitat quality at three sites in Narragansett Bay, Rhode Island. The upper bay site, Gaspee Point, had the highest population density and concentration of total ni...
Marine biogenic source of atmospheric organic nitrogen in the subtropical North Atlantic
Altieri, Katye E.; Fawcett, Sarah E.; Peters, Andrew J.; Sigman, Daniel M.; Hastings, Meredith G.
2016-01-01
Global models estimate that the anthropogenic component of atmospheric nitrogen (N) deposition to the ocean accounts for up to a third of the ocean’s external N supply and 10% of anthropogenic CO2 uptake. However, there are few observational constraints from the marine atmospheric environment to validate these findings. Due to the paucity of atmospheric organic N data, the largest uncertainties related to atmospheric N deposition are the sources and cycling of organic N, which is 20–80% of total N deposition. We studied the concentration and chemical composition of rainwater and aerosol organic N collected on the island of Bermuda in the western North Atlantic Ocean over 18 mo. Here, we show that the water-soluble organic N concentration ([WSON]) in marine aerosol is strongly correlated with surface ocean primary productivity and wind speed, suggesting a marine biogenic source for aerosol WSON. The chemical composition of high-[WSON] aerosols also indicates a primary marine source. We find that the WSON in marine rain is compositionally different from that in concurrently collected aerosols, suggesting that in-cloud scavenging (as opposed to below-cloud “washout”) is the main contributor to rain WSON. We conclude that anthropogenic activity is not a significant source of organic N to the marine atmosphere over the North Atlantic, despite downwind transport from large pollution sources in North America. This, in conjunction with previous work on ammonium and nitrate, leads to the conclusion that only 27% of total N deposition to the global ocean is anthropogenic, in contrast to the 80% estimated previously. PMID:26739561
Mundo, Ignacio A; Wiegand, Thorsten; Kanagaraj, Rajapandian; Kitzberger, Thomas
2013-07-15
Fire management requires an understanding of the spatial characteristics of fire ignition patterns and how anthropogenic and natural factors influence ignition patterns across space. In this study we take advantage of a recent fire ignition database (855 points) to conduct a comprehensive analysis of the spatial pattern of fire ignitions in the western area of Neuquén province (57,649 km(2)), Argentina, for the 1992-2008 period. The objectives of our study were to better understand the spatial pattern and the environmental drivers of the fire ignitions, with the ultimate aim of supporting fire management. We conducted our analyses on three different levels: statistical "habitat" modelling of fire ignition (natural, anthropogenic, and all causes) based on an information theoretic approach to test several competing hypotheses on environmental drivers (i.e. topographic, climatic, anthropogenic, land cover, and their combinations); spatial point pattern analysis to quantify additional spatial autocorrelation in the ignition patterns; and quantification of potential spatial associations between fires of different causes relative to towns using a novel implementation of the independence null model. Anthropogenic fire ignitions were best predicted by the most complex habitat model including all groups of variables, whereas natural ignitions were best predicted by topographic, climatic and land-cover variables. The spatial pattern of all ignitions showed considerable clustering at intermediate distances (<40 km) not captured by the probability of fire ignitions predicted by the habitat model. There was a strong (linear) and highly significant increase in the density of fire ignitions with decreasing distance to towns (<5 km), but fire ignitions of natural and anthropogenic causes were statistically independent. A two-dimensional habitat model that quantifies differences between ignition probabilities of natural and anthropogenic causes allows fire managers to delineate target areas for consideration of major preventive treatments, strategic placement of fuel treatments, and forecasting of fire ignition. The techniques presented here can be widely applied to situations where a spatial point pattern is jointly influenced by extrinsic environmental factors and intrinsic point interactions. Copyright © 2013 Elsevier Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Knöller, K.; Trettin, R.; Strauch, G.
2005-11-01
The hydrochemical composition of groundwater and the isotopic composition of sulphur compounds in sediments (34S of sulphide, inorganic sulphate) and groundwater (34S, 18O of dissolved sulphate) have been investigated to reveal the reasons for elevated concentrations of dissolved groundwater sulphate in the drinking water catchment area of Torgau-Mockritz (Germany).The three most important anthropogenic sources of sulphate identified in this study are historic atmospheric sulphate deposition, predominantly of anthropogenic origin, inorganic fertilization, and dissolution of gypsum from waste dumps. Owing to their overlapping isotopic range, no clear differentiation between the individual anthropogenic sources is possible. Sulphate from the oxidation of sedimentary sulphides, however, was recognized by its negative sulphur isotope signature (34S < - 5).The mobilization of sulphate from different soil sulphur species is closely connected with variable isotopic fractionations, resulting in a wide isotopic variation range for the sulphate entering the saturated zone. Generally, sulphur and oxygen isotope ratios of the dissolved groundwater sulphate range from -19 to +37 (Vienna Cañon Diablo troilite) and from -2 to +19 (Vienna standard mean ocean water), respectively. Sulphate from the majority of groundwater samples can be assigned to anthropogenic sources. Sulphate from sulphide oxidation is especially present in samples from the upper sampling level and the groundwater surface. Sulphate concentrations above 700 mg l-1 are mostly caused by the oxidation of sulphide. Sulphate that occurs in low and moderate concentrations dominantly originates from anthropogenic sources.34S distribution patterns were used to locate the sources for the elevated sulphate concentrations in the raw water. It was shown that the sulphate is not mobilized in the immediate vicinity of the production wells. Rather, it originates in an area 1.5 km west of the intake. The main mobilization mechanism there is the oxidation of reduced sedimentary sulphur species.Beyond its local significance, this study presents a general example how changes in the sulphur cycle indicate major, anthropogenically induced alterations of the hydrochemical situation in catchment areas. Copyright
The observed influence of local anthropogenic pollution on northern Alaskan cloud properties
NASA Astrophysics Data System (ADS)
Maahn, Maximilian; de Boer, Gijs; Creamean, Jessie M.; Feingold, Graham; McFarquhar, Greg M.; Wu, Wei; Mei, Fan
2017-12-01
Due to their importance for the radiation budget, liquid-containing clouds are a key component of the Arctic climate system. Depending on season, they can cool or warm the near-surface air. The radiative properties of these clouds depend strongly on cloud drop sizes, which are governed in part by the availability of cloud condensation nuclei. Here, we investigate how cloud drop sizes are modified in the presence of local emissions from industrial facilities at the North Slope of Alaska. For this, we use aircraft in situ observations of clouds and aerosols from the 5th Department of Energy Atmospheric Radiation Measurement (DOE ARM) Program's Airborne Carbon Measurements (ACME-V) campaign obtained in summer 2015. Comparison of observations from an area with petroleum extraction facilities (Oliktok Point) with data from a reference area relatively free of anthropogenic sources (Utqiaġvik/Barrow) represents an opportunity to quantify the impact of local industrial emissions on cloud properties. In the presence of local industrial emissions, the mean effective radii of cloud droplets are reduced from 12.2 to 9.4 µm, which leads to suppressed drizzle production and precipitation. At the same time, concentrations of refractory black carbon and condensation nuclei are enhanced below the clouds. These results demonstrate that the effects of anthropogenic pollution on local climate need to be considered when planning Arctic industrial infrastructure in a warming environment.
Forecasting future phosphorus export to the Laurentian Great Lakes from land-derived nutrient inputs
NASA Astrophysics Data System (ADS)
LaBeau, M. B.; Robertson, D. M.; Mayer, A. S.; Pijanowski, B. C.
2011-12-01
Anthropogenic use of the land through agricultural and urban activities has significantly increased phosphorus loading to rivers that flow to the Great Lakes. Phosphorus (P) is a critical element in the eutrophication of the freshwater ecosystems, most notably the Great Lakes. To better understand factors influencing phosphorus delivery to aquatic systems and thus their potential harmful effects to lake ecosystems, models that predict P export should incorporate account for changing changes in anthropogenic activities. Land-derived P from high yielding sources, such as agriculture and urban areas, affect eutrophication at various scales (e.g. specific bays to all of Lake Erie). SPARROW (SPAtially Referenced Regression On Watershed attributes) is a spatially explicit watershed model that has been used to understand linkages between land-derived sources and nutrient transport to the Great Lakes. The Great Lakes region is expected to experience a doubling of urbanized areas along with a ten percent increase in agricultural use over the next 40 years, which is likely to increase P loading. To determine how these changes will impact P loading, SPARROW have been developed that relate changes in land use to changes in nutrient sources, including relationships between row crop acreage and fertilizer intensity and urban land use and point source intensity. We used land use projections from the Land Transformation Model, a, spatially explicit, neural-net based land change model. Land use patterns from current to 2040 were used as input into HydroSPARROW, a forecasting tool that enables SPARROW to simulate the effects of various land-use and climate scenarios. Consequently, this work is focusing on understanding the effects of how specific agriculture and urbanization activities affect P loading in the watersheds of the Laurentian Great Lakes to potentially find strategies to reduce the extent and severity of future eutrophication.
Diurnal and seasonal variation of various carbon fluxes from an urban tower platform in Houston, TX
NASA Astrophysics Data System (ADS)
Schade, G. W.; Werner, N.; Hale, M. C.
2013-12-01
We measured carbon fluxes (CO2, CO, VOCs) from a tall lattice tower in Houston between 2007 and 2009, and 2011-2013. We present results from various analyses of (i) anthropogenic and biogenic CO2 fluxes using a quadrant segregation technique, (ii) seasonal and multi-year changes of CO fluxes as related to car traffic and industrial sources, and (iii) the accuracy of, and usefulness of a bulk flux footprint model to quantify pentane emissions form a distant source in comparison to permitted emission levels. Segregated and net anthropogenic CO2 fluxes were dominated by car traffic but industrial sources were identified as well. Emissions sank to minimal levels after hurricane Ike had passed over Houston, causing a traffic shutdown and lower population density. Segregated biogenic fluxes showed a clear seasonal variation with photosynthetic activity between April and November, and large effects of the 2011 Texas drought due to negligible irrigation in the study area. Carbon monoxide fluxes, measured via a flux gradient technique, are even stronger dominated by car traffic than CO2 fluxes and serve as a traffic tracer. Our data show a continued drop in emissions over time, seasonal changes with higher emissions during winter, and local influences due to industrial emissions. Lastly, we present the results of a tracer release study and a single point source quantification to test a bulk footprint model in this complex urban area. Known releases of volatile acetone and MEK were compered to measured fluxes using a REA-GC-FID system, and permit emissions of pentane from a foam plastics manufacturing facility were compared to measured pentane fluxes. Both comparisons reveal a surprisingly accurate performance of the footprint model within a factor of 2.
NASA Astrophysics Data System (ADS)
Sanyal, S.; Wuebbles, D. J.
2017-12-01
In this study, the focus is on how global changes in climate and emissions will affect the U.S. air quality, especially on fine particulate matter and ozone, projecting their future trends and quantifying key source attribution. We are conducting three primary experiments : (1) historical simulations for period 1994-2013 to establish the credibility of the system and refine process-level understanding of U.S. regional air quality; (2) projections for period 2041-2060 to quantify individual and combined impacts of global climate and emissions changes under multiple scenarios; (3) sensitivity analyses to determine future changes in pollution sources and their relative contributions from anthropogenic and natural emissions, long-range pollutant transport, and climate change effects. Here we will present the result from the first experiment with the global model CESM1.2 (with fully coupled chemistry using CAM-chem5) driven by NASA Modern-Era Retrospective analysis for Research and Applications (MERRA) reanalysis data at 0.9o x 1.25o resolution. We will present the comparison between the results from model simulation with observation data from EPA database. Since there is always a challenge in comparing gridded prediction from model data with point data from the observation databases, because the model simulations calculate the average outcome over a grid for a given set of conditions while the stochastic component (e.g. sub-grid variations) embedded in the observations are not accounted for, we are using extensive statistical measure to do the comparison. We will also determine relative contributions from multiscale (local, regional, global) processes, major source regions (Mexico, Canada, Asia, Africa) and types (natural, anthropogenic) and associated uncertainties (climate decadal oscillations/interannual variations, emissions and model structure errors).
Source Partitioning of Methane Emissions and its Seasonality in the U.S. Midwest
NASA Astrophysics Data System (ADS)
Chen, Zichong; Griffis, Timothy J.; Baker, John M.; Millet, Dylan B.; Wood, Jeffrey D.; Dlugokencky, Edward J.; Andrews, Arlyn E.; Sweeney, Colm; Hu, Cheng; Kolka, Randall K.
2018-02-01
The methane (CH4) budget and its source partitioning are poorly constrained in the Midwestern United States. We used tall tower (185 m) aerodynamic flux measurements and atmospheric scale factor Bayesian inversions to constrain the monthly budget and to partition the total budget into natural (e.g., wetlands) and anthropogenic (e.g., livestock, waste, and natural gas) sources for the period June 2016 to September 2017. Aerodynamic flux observations indicated that the landscape was a CH4 source with a mean annual CH4 flux of +13.7 ± 0.34 nmol m-2 s-1 and was rarely a net sink. The scale factor Bayesian inversion analyses revealed a mean annual source of +12.3 ± 2.1 nmol m-2 s-1. Flux partitioning revealed that the anthropogenic source (7.8 ± 1.6 Tg CH4 yr-1) was 1.5 times greater than the bottom-up gridded United States Environmental Protection Agency inventory, in which livestock and oil/gas sources were underestimated by 1.8-fold and 1.3-fold, respectively. Wetland emissions (4.0 ± 1.2 Tg CH4 yr-1) were the second largest source, accounting for 34% of the total budget. The temporal variability of total CH4 emissions was dominated by wetlands with peak emissions occurring in August. In contrast, emissions from oil/gas and other anthropogenic sources showed relatively weak seasonality.
Variation of atmospheric carbon monoxide over the Arctic Ocean during summer 2012
NASA Astrophysics Data System (ADS)
Park, Keyhong; Siek Rhee, Tae; Emmons, Louisa
2014-05-01
Atmospheric carbon monoxide (CO) plays an important role in ozone-related chemistry in the troposphere, especially under low-NOx conditions like the open ocean. During summer 2012, we performed a continuous high-resolution (0.1Hz) shipboard measurement of atmospheric CO over the Arctic Ocean. We also simulated the observation using a 3-D global chemical transport model (the Model for OZone And Related chemical Tracers-4; MOZART-4) for further analysis of the observed results. In the model, tags for each sources and emission regions of CO are applied and this enables us to delineate the source composition of the observations. Along with the observed variation of CO concentration during the research cruise, we will present in detailed analysis of the variation of source components and change of regional contributions. We found large (~80ppbv) variation of CO concentration in the Arctic Ocean which is mostly influenced by the variation of biomass burning activity. The contribution of anthropogenic emission is limited over the Arctic Ocean, although the northeast Asian anthropogenic emission shows a dominant component of transported anthropogenic CO. Also, our analysis shows, near the Bering Strait, Europe is the main emission region for anthropogenic CO.
NASA Astrophysics Data System (ADS)
Dickerson, R. R.; Ren, X.; Shepson, P. B.; Salmon, O. E.; Brown, S. S.; Thornton, J. A.; Whetstone, J. R.; Salawitch, R. J.; Sahu, S.; Hall, D.; Grimes, C.; Wong, T. M.
2015-12-01
Urban areas are responsible for a major component of the anthropogenic greenhouse gas (GHG) emissions. Quantification of urban GHG fluxes is important for establishing scientifically sound and cost-effective policies for mitigating GHGs. Discrepancies between observations and model simulations of GHGs suggest uncharacterized sources in urban environments. In this work, we analyze and quantify fluxes of CO2, CH4, CO (and other trace species) from the Baltimore-Washington area based on the mass balance approach using the two-aircraft observations conducted in February-March 2015. Estimated fluxes from this area were 110,000±20,000 moles s-1 for CO2, 700±330 moles s-1 for CH4, and 535±188 moles s-1 for CO. This implies that methane is responsible for ~20% of the climate forcing from these cities. Point sources of CO2 from four regional power plants and one point source of CH4 from a landfill were identified and the emissions from these point sources were quantified based on the aircraft observation and compared to the emission inventory data. Methane fluxes from the Washington area were larger than from the Baltimore area, indicating a larger leakage rate in the Washington area. The ethane-to-methane ratios, with a mean of 3.3%, in the limited canister samples collected during the flights indicate that natural gas leaks and the upwind oil and natural gas operations are responsible for a substantial fraction of the CH4 flux. These observations will be compared to models using Ensemble Kalman Filter Assimilation techniques.
The chemical composition and fluxes of atmospheric wet deposition at four sites in South Africa
NASA Astrophysics Data System (ADS)
Conradie, E. H.; Van Zyl, P. G.; Pienaar, J. J.; Beukes, J. P.; Galy-Lacaux, C.; Venter, A. D.; Mkhatshwa, G. V.
2016-12-01
South Africa is the economic hub of southern Africa and is regarded as an important source region of atmospheric pollutants. A nitrogen dioxide (NO2) hotspot is clearly visible from space over the South African Mpumalanga Highveld, while South Africa is also regarded as the 9th largest anthropogenic sulphur (S) emitting country. Notwithstanding the importance of South Africa with regard to nitrogen (N) and S emissions, very limited data has been published on the chemical composition of wet deposition for this region. This paper presents the concentrations of sodium (Na+), ammonium (NH4+), potassium (K+), calcium (Ca2+), magnesium (Mg2+), nitrate (NO3-), chloride (Cl-), sulphate (SO42-) and water-soluble organic acids (OA) in the wet deposition samples collected between 2009 and 2014 at four South African IDAF (IGAC DEBITS Africa) sites, which are regarded as regional representatives of the north-eastern interior. Also, wet deposition fluxes of the ten ions are calculated and presented in this paper. The results show that the total ionic concentrations and fluxes of wet deposition were much higher at the two sites closer to anthropogenic emissions, while the pH of wet deposition at these two sites were lower compared to that of the two sites that were less impacted by anthropogenic emissions. . The major sources of the ten ions included marine, terrigenous (crust), fossil fuel combustion, agriculture and biomass burning. Significant contributions from fossil fuel combustion were determined for the two sites in close proximity to anthropogenic source regions. The results of back trajectory analysis, however, did indicate that the two remote sites are also affected by air masses passing over the source region through anti-cyclonic recirculation. The largest contributions at the two sites distant from the anthropogenic source regions were marine sources, while the impact of biomass burning was also more significant at the remote sites. Comparison to previous wet deposition measurements at the South African IDAF sites indicated increases in the wet deposition fluxes of S and N, and more wet deposition events with lower pH. This could be ascribed to a significant increase in anthropogenic activities and population growth in this part of South Africa with an associated increase in energy demand.
NASA Astrophysics Data System (ADS)
Kangasaho, V. E.; Tsuruta, A.; Aalto, T.; Backman, L. B.; Houweling, S.; Krol, M. C.; Peters, W.; van der Laan-Luijkx, I. T.; Lienert, S.; Joos, F.; Dlugokencky, E. J.; Michael, S.; White, J. W. C.
2017-12-01
The atmospheric burden of CH4 has more than doubled since preindustrial time. Evaluating the contribution from anthropogenic and natural emissions to the global methane budget is of great importance to better understand the significance of different sources at the global scale, and their contribution to changes in growth rate of atmospheric CH4 before and after 2006. In addition, observations of δ13C-CH4 suggest an increase in natural sources after 2006, which matches the observed increase and variation of CH4 abudance. Methane emission sources can be identified using δ13C-CH4, because different sources produce methane with process-specific isotopic signatures. This study focuses on inversion model based estimates of global anthropogenic and natural methane emission rates to evaluate the existing methane emission estimates with a new δ13C-CH4 inversion system. In situ measurements of atmospheric methane and δ13C-CH4 isotopic signature, provided by the NOAA Global Monitoring Division and the Institute of Arctic and Alpine Research, will be assimilated into the CTDAS-13C-CH4. The system uses the TM5 atmospheric transport model as an observation operator, constrained by ECMWF ERA Interim meteorological fields, and off-line TM5 chemistry fields to account for the atmospheric methane sink. LPX-Bern DYPTOP ecosystem model is used for prior natural methane emissions from wetlands, peatlands and mineral soils, GFED v4 for prior fire emissions and EDGAR v4.2 FT2010 inventory for prior anthropogenic emissions. The EDGAR antropogenic emissions are re-divided into enteric fermentation and manure management, landfills and waste water, rice, coal, oil and gas, and residential emissions, and the trend of total emissions is scaled to match optimized anthropogenic emissions from CTE-CH4. In addition to these categories, emissions from termites and oceans are included. Process specific δ13C-CH4 isotopic signatures are assigned to each emission source to estimate 13CH4 fraction in CH4 emissions. Among the priors, anthropogenic and natural emissions are optimized and others are directly imposed from the prior. A detailed emission estimates of antropogenic and natural CH4 emissions will be constructed in order to provide a more comprehensive understanding of methane emission source divisions.
Methane Dynamics in Flooded Lands
Methane (CH4) is the second most important anthropogenic greenhouse gas with a heat trapping capacity 34 times greater than that of carbon dioxide on a100 year time scale. Known anthropogenic CH4 sources include livestock production, rice agriculture, landfills, and natural gas m...
Measuring and managing reservoir greenhouse gas emissions
Methane (CH4) is the second most important anthropogenic greenhouse gas with a heat trapping capacity 34 times greater than that of carbon dioxide on a 100 year time scale. Known anthropogenic CH4 sources include livestock production, rice agriculture, landfills, and natural gas...
Physical and Chemical Properties of Anthropogenic Aerosols: An overview
A wide variety of anthropogenic sources emit fine aerosols to the atmosphere. The physical and chemical properties of these aerosols are of interest due to their influence on climate, human health, and visibility. Aerosol chemical composition is complex. Combustion aerosols can c...
Hochmair, Hartwig H; Scheffrahn, Rudolf H
2010-08-01
Marine vessels have been implicated in the anthropogenic dispersal of invasive termites for the past 500 yr. It has long been suspected that two invasive termites, the Formosan subterranean termite, Coptotermes formosanus Shiraki, and Coptotermes gestroi (Wasmann) (Isoptera: Rhinotermitidae), were introduced to and dispersed throughout South Florida by sailboats and yachts. We compared the distances between 190 terrestrial point records for Formosan subterranean termite, 177 records for C. gestroi, and random locations with the nearest marine dockage by using spatial analysis. Results show that the median distance to nearest docks associated with C. gestroi is significantly smaller than for the random points. Results also reveal that the median distance to nearest docks associated with Formosan subterranean termite is significantly smaller than for the random points. These results support the hypothesis that C. gestroi and Formosan subterranean termite are significantly closer to potential infested boat locations, i.e., marine docks, than random points in these urban areas. The results of our study suggest yet another source of aggregation in the context of exotic species, namely, hubs for pleasure boating.
Re-assessing the surface cycling of molybdenum and rhenium
NASA Astrophysics Data System (ADS)
Miller, Christian A.; Peucker-Ehrenbrink, Bernhard; Walker, Brett D.; Marcantonio, Franco
2011-11-01
We re-evaluate the cycling of molybdenum (Mo) and rhenium (Re) in the near-surface environment. World river average Mo and Re concentrations, initially based on a handful of rivers, are calculated using 38 rivers representing five continents, and 11 of 19 large-scale drainage regions. Our new river concentration estimates are 8.0 nmol kg -1 (Mo), and 16.5 pmol kg -1 (Re, natural + anthropogenic). The linear relationship of dissolved Re and SO42- in global rivers ( R2 = 0.76) indicates labile continental Re is predominantly hosted within sulfide minerals and reduced sediments; it also provides a means of correcting for the anthropogenic contribution of Re to world rivers using independent estimates of anthropogenic sulfate. Approximately 30% of Re in global rivers is anthropogenic, yielding a pre-anthropogenic world river average of 11.2 pmol Re kg -1. The potential for anthropogenic contribution is also seen in the non-negligible Re concentrations in precipitation (0.03-5.9 pmol kg -1), and the nmol kg -1 level Re concentrations of mine waters. The linear Mo- SO42- relationship ( R2 = 0.69) indicates that the predominant source of Mo to rivers is the weathering of pyrite. An anthropogenic Mo correction was not done as anthropogenically-influenced samples do not display the unambiguous metal enrichment observed for Re. Metal concentrations in high temperature hydrothermal fluids from the Manus Basin indicate that calculated end-member fluids (i.e. Mg-free) yield negative Mo and Re concentrations, showing that Mo and Re can be removed more quickly than Mg during recharge. High temperature hydrothermal fluids are unimportant sinks relative to their river sources 0.4% (Mo), and 0.1% (pre-anthropogenic Re). We calculate new seawater response times of 4.4 × 10 5 yr ( τMo) and 1.3 × 10 5 yr ( τRe, pre-anthropogenic).
Significant human impact on the flux and δ(34)S of sulfate from the largest river in North America.
Killingsworth, Bryan A; Bao, Huiming
2015-04-21
Riverine dissolved sulfate (SO4(2-)) flux and sulfur stable isotope composition (δ(34)S) yield information on the sources and processes affecting sulfur cycling on different spatial and temporal scales. However, because pristine preindustrial natural baselines of riverine SO4(2-) flux and δ(34)S cannot be directly measured, anthropogenic impact remains largely unconstrained. Here we quantify natural and anthropogenic SO4(2-) flux and δ(34)S for North America's largest river, the Mississippi, by means of an exhaustive source compilation and multiyear monitoring. Our data and analysis show that, since before industrialization to the present, Mississippi River SO4(2-) has increased in flux from 7.0 to 27.8 Tg SO4(2-) yr(-1), and in mean δ(34)S from -5.0‰, within 95% confidence limits of -14.8‰ to 4.1‰ (assuming normal distribution for mixing model input parameters), to -2.7 ± 1.6‰, reflecting an impressive footprint of bedrocks particular to this river basin and human activities. Our first-order modern Mississippi River sulfate partition is 25 ± 6% natural and 75% ± 6% anthropogenic sources. Furthermore, anthropogenic coal usage is implicated as the dominant source of modern Mississippi River sulfate, with an estimated 47 ± 5% and 13% of total Mississippi River sulfate due to coal mining and burning, respectively.
McMahon, G.; Harned, D.A.
1998-01-01
Environmental settings were defined, through an overlay process, as areas of coincidence between categories of three mapped variables - land use, surficial geology, and soil drainage characteristics. Expert judgment was used in selecting factors thought to influence sediment and nutrient concentrations in the Albemarle-Pamlico drainage area. This study's findings support the hypothesis that environmental settings defined using these three variables can explain variations in the concentration of certain sediment and nutrient constituents. This finding underscores the importance of developing watershed management plans that account for differences associated with the mosaic of natural and anthropogenic factors that define a basin's environmental setting. At least in the case of sediment and nutrients in the Albemarle-Pamlico region, a watershed management plan that focuses only on anthropogenic factors, such as point-source discharges, and does not account for natural characteristics of a watershed and the influences of these characteristics on water quality, may lead to water-quality goals that are over- or underprotective of key environmental features and to a misallocation of the resources available for environmental protection.
Kuo, Li-Jung; Lee, Chon-Lin; Louchouarn, Patrick; Huh, Chih-An; Liu, James T; Chen, Jian-Cheng; Lee, Kun-Je
2014-09-15
A 100-year history of human and natural disturbances in southwestern Taiwan was reconstructed using a suite of molecular markers in four dated sediment cores from the upper slope region off the Gaoping River mouth. Trends in polycyclic aromatic hydrocarbons (PAHs) tracked Taiwan's industrialization/urbanization starting in the 1970s, and the enactment of environmental regulatory policies thereafter. The predominant pyrogenic sources include vehicular, smelter, and coal combustion but spatial differences are observed among sub-regions of the shelf. Profiles of lignin oxidation products (LOPs) point to a significant increase in terrestrial organic matter inputs driven by land development after the 1970s. Low lignin diagenetic signature ratios [(Ad/Al)v] in all sediments suggest quick transport of fresh plant material from land to sea via mountainous rivers. Shifts in PAHs, LOPs, and radionuclides in recent sediments reveal the deposition of turbidites resulting from typhoon-induced floods. Multiproxy analysis illustrates the interplay between anthropogenic activities and natural processes. Copyright © 2014 Elsevier Ltd. All rights reserved.
NASA Technical Reports Server (NTRS)
Roselle, Shawn J.; Schere, Kenneth L.; Chu, Shao-Hang
1994-01-01
There is increasing recognition that controls on NO(x) emissions may be necessary, in addition to existing and future Volatile Organic Compounds (VOC) controls, for the abatement of ozone (O3) over portions of the United States. This study compares various combinations of anthropogenic NO(x) and VOC emission reductions through a series of model simulations. A total of 6 simulations were performed with the Regional Oxidant Model (ROM) for a 9-day period in July 1988. Each simulation reduced anthropogenic NO(x) and VOC emissions across-the-board by different amounts. Maximum O3 concentrations for the period were compared between the simulations. Comparison of the simulations suggests that: (1) NO(x) controls may be more effective than VOC controls in reducing peak O3 over most of the eastern United States; (2) VOC controls are most effective in urban areas having large sources of emissions; (3) NO(x) controls may increase O3 near large point sources; and (4) the benefit gained from increasing the amount of VOC controls may lessen as the amount of NO(x) control is increased. This paper has been reviewed in accordance with the U.S. Environmental Protection Agency's peer and administrative review policies and approved for presentation and publication. Mention of trade names or commercial products does not constitute endorsement or recommendation for use.
Eqani, Syed Ali Musstjab Akber Shah; Kanwal, Ayesha; Bhowmik, Avit Kumar; Sohail, Mohammad; Ullah, Rizwan; Ali, Syeda Maria; Alamdar, Ambreen; Ali, Nadeem; Fasola, Mauro; Shen, Heqing
2016-06-01
This study aims to assess the spatial patterns of selected dust-borne trace elements alongside the river Indus Pakistan, their relation with anthropogenic and natural sources, and the potential risk posed to human health. The studied elements were found in descending concentrations: Mn, Zn, Pb, Cu, Ni, Cr, Co, and Cd. The Index of Geo-accumulation indicated that pollution of trace metals were higher in lower Indus plains than on mountain areas. In general, the toxic elements Cr, Mn, Co and Ni exhibited altitudinal trends (P < 0.05). The few exceptions to this trend were the higher values for all studied elements from the northern wet mountainous zone (low lying Himalaya). Spatial PCA/FA highlighted that the sources of different trace elements were zone specific, thus pointing to both geological influences and anthropogenic activities. The Hazard Index for Co and for Mn in children exceeded the value of 1 only in the riverine delta zone and in the southern low lying zone, whereas the Hazard Index for Pb was above the bench mark for both children and adults (with few exceptions) in all regions, thus indicating potential non-carcinogenic health risks. These results will contribute towards the environmental management of trace metal(s) with potential risk for human health throughout Pakistan. Copyright © 2016 Elsevier Ltd. All rights reserved.
Modeling urban air pollution in Budapest using WRF-Chem model
NASA Astrophysics Data System (ADS)
Kovács, Attila; Leelőssy, Ádám; Lagzi, István; Mészáros, Róbert
2017-04-01
Air pollution is a major problem for urban areas since the industrial revolution, including Budapest, the capital and largest city of Hungary. The main anthropogenic sources of air pollutants are industry, traffic and residential heating. In this study, we investigated the contribution of major industrial point sources to the urban air pollution in Budapest. We used the WRF (Weather Research and Forecasting) nonhydrostatic mesoscale numerical weather prediction system online coupled with chemistry (WRF-Chem, version 3.6).The model was configured with three nested domains with grid spacings of 15, 5 and 1 km, representing Central Europe, the Carpathian Basin and Budapest with its surrounding area. Emission data was obtained from the National Environmental Information System. The point source emissions were summed in their respective cells in the second nested domain according to latitude-longitude coordinates. The main examined air pollutants were carbon monoxide (CO) and nitrogen oxides (NOx), from which the secondary compound, ozone (O3) forms through chemical reactions. Simulations were performed under different weather conditions and compared to observations from the automatic monitoring site of the Hungarian Air Quality Network. Our results show that the industrial emissions have a relatively weak role in the urban background air pollution, confirming the effect of industrial developments and regulations in the recent decades. However, a few significant industrial sources and their impact area has been demonstrated.
NASA Astrophysics Data System (ADS)
Pacella, S. R.
2016-02-01
Ocean acidification has recently been highlighted as a major stressor for coastal organisms. Further work is needed to assess the role of anthropogenic nutrient additions in eutrophied systems on local biological processes, and how this interacts with CO2 emission-driven acidification. This study sought to distinguish changes in pH caused by natural versus anthropogenically affected processes. We quantified the variability in water column pH attributable to primary production and respiration fueled by anthropogenically derived nitrogen in a shallow nearshore area. Two study sites were located in shallow subtidal areas of the Snohomish River estuary, a eutrophic system located in central Puget Sound, Washington. These sites were chosen due to the presence of heavy agricultural activity, urbanized areas with associated waste water treatment, as well as influence from deep, high CO2 marine waters transported through the Strait of Juan de Fuca and upwelled into the area during spring and summer. Data was collected from July-December 2015 utilizing continuous moorings and discrete water column sampling. Analysis of stable isotopes, δ15N, δ18O-NO3, δ15N-NH4, was used to estimate the relative contributions of anthropogenic versus upwelled marine nitrogen sources. Continuous monitoring of pH, dissolved oxygen, temperature, and salinity was conducted at both study sites to link changes in nutrient source and availability with changes in pH. We predicted that isotope data would indicate greater contributions of nitrogen from agriculture and wastewater rather than upwelling in the shallow, nearshore study sites. This study seeks to distinguish the relative magnitude of pH change stimulated by anthropogenic versus natural sources of nitrogen to inform public policy decisions in critically important nearshore ecosystems.
GOSAT Observations of Anthropogenic Emission of Carbon Dioxide and Methane
NASA Astrophysics Data System (ADS)
Janardanan Achari, R.; Maksyutov, S. S.; Oda, T.; Saito, M.; W Kaiser, J.; Ganshin, A.; Matsunaga, T.; Yoshida, Y.; Yokota, T.
2016-12-01
Carbon dioxide (CO2) and methane (CH4) are the most important greenhouse gases in terms of radiative forcing. Anthropogenic activities such as combustion of fossil fuel (for CO2) and gas leakage, animal agriculture, rice cultivation and landfill emissions (CH4), are considered to be major sources of those emissions. Still, emission data usually depend on national emission reports, which are seldom evaluated independently. Here we present a method for delineating anthropogenic contribution to global atmospheric CO2 (2009-2014) and CH4 (2009-2012) fields using GOSAT observations of column-average dry air mole fractions (XCO2 and XCH4) and atmospheric transport model simulations using high-resolution emission inventories. The CO2 and CH4 concentration enhancement due to anthropogenic activities, are estimated with the transport model at all GOSAT observation locations using high-resolution emission inventories (ODIAC for CO2 and EDGAR for CH4). Based on this estimate, using a threshold value, the observations are classified into two categories: data influenced by the anthropogenic sources and those not including them. To extract concentration enhancements due to the anthropogenic emissions, we define a clean background (the averaged values for the data free from contamination) in 10°×10° regions over the globe and are subtracted from the individual observational data including the anthropogenic contamination. Thus the anomalies contain contributions from anthropogenic sources. These anomalies are binned and analyzed for continental scale regions and countries. For CO2, we have found global and regional linear relationships between model and observed anomalies especially for Eurasia and North America. The analysis for East Asian region showed a systematic bias that is comparable in magnitude to the reported uncertainties in emission inventories in that region. In the case of CH4, we also found a good match between inventory-based estimates and GOSAT observations for continental regions and large countries. In ideal case, the regression slope between modeled and observed anomalies can be a correction factor for the emission inventory. If sufficient number of satellite observations is available, this method will be a useful tool for monitoring greenhouse gas emissions.
Natural and anthropogenic factors affecting the groundwater quality in Serbia.
Devic, Gordana; Djordjevic, Dragana; Sakan, Sanja
2014-01-15
Various chemometric techniques were used to analyze the quality of groundwater data sets. Seventeen water quality parameters: the cations Na, K, Ca, Mg, the anions Cl, SO4, NO3, HCO3 and nine trace elements Pb, As, Mn, Ni, Cu, Cd, Fe, Zn and Cr were measured at 66 different key sampling sites in ten representative areas (low land-Northern Autonomous Province of Serbia, Vojvodina and central Serbia) for the summer period of 2009. HCA grouped the sample sites into four clusters based on the similarities of the characteristics of the groundwater quality. DA showed two parameters, HCO3 and Zn, affording more than 90% correct assignments in the spatial analysis of four/three different regions in Serbia. Factor analysis was applied on the log-transformed data sets and allowed the identification of a reduced number of factors with hydrochemical meaning. The results showed severe pollution with Mn, As, NO3, Ni, Pb whereby anthropogenic origin of these contaminants was indicated. The pollution comes from both scattered point sources (industrial and urban effluent) and diffuse source agricultural activity. These samples may not be suitable for human consumption; the water quality belongs to class III/IV (contaminated). The Fe anomalies (7.1mg/L) in the water from the Vetrnica site can be attributed to natural sources, such as the dissolution of rock masses and rock fragments. The serious groundwater contamination with As (25.7-137.8 μg/L) in the area of Banat (Northern Autonomous Province of Serbia, Vojvodina) and a sample No. 9 at the Great Morava River requires urgent attention. © 2013.
Source Attribution of Tropospheric Ozone using a Global Model
NASA Astrophysics Data System (ADS)
Coates, J.; Lupascu, A.; Butler, T. M.; Zhu, S.
2016-12-01
Tropospheric ozone is both a short-lived climate forcing pollutant and a radiatively active greenhouse gas. Ozone is not directly emitted into the troposphere but photochemically produced from chemical reactions involving nitrogen oxides (NOx) and volatile organic compounds (VOCs). Emissions of ozone precursors (NOx and VOCs) have both natural and anthropogenic sources and may be transported away from their sources to produce ozone downwind. Also, transport of ozone from the stratosphere into the troposphere also influences tropospheric ozone levels in some regions. Attributing ozone concentrations to the contributions from different sources would indicate the effects of locally emitted or transported precursors on ozone levels in specific regions. This information could be used to inform the emission reduction strategies of ozone precursors by indicating which emission sources could be targeted for effective reductions thus reducing the burden of ozone pollution. We use a "tagging" approach within the CESM global model to attribute ozone levels to their source emissions. We use different tags to quantify the impact from natural (soils, lightning, stratospheric transport) and anthropogenic (aircraft, biomass burning) sources of NOx and VOCs (including methane) on ozone levels. These source sectors of different global regions are assigned based on the global emissions specified by HTAPv2.2. Using these results, we develop a transboundary source-receptor relationship of ozone concentration to its precursor emission regions. Additionally, the transport of ozone precursors from regional anthropogenic sources is analysed to illustrate the extent to which mitigation strategies of regional emissions aid in mitigating global ozone levels.
NASA Astrophysics Data System (ADS)
Shepson, P. B.; Lavoie, T. N.; Kerlo, A. E.; Stirm, B. H.
2016-12-01
Understanding the contribution of anthropogenic activities to atmospheric greenhouse gas concentrations requires an accurate characterization of emission sources. Previously, we have reported the use of a novel aircraft-based mass balance measurement technique to quantify greenhouse gas emission rates from point and area sources, however, the accuracy of this approach has not been evaluated to date. Here, an assessment of method accuracy and precision was performed by conducting a series of six aircraft-based mass balance experiments at a power plant in southern Indiana and comparing the calculated CO2 emission rates to the reported hourly emission measurements made by continuous emissions monitoring systems (CEMS) installed directly in the exhaust stacks at the facility. For all flights, CO2 emissions were quantified before CEMS data were released online to ensure unbiased analysis. Additionally, we assess the uncertainties introduced to the final emission rate caused by our analysis method, which employs a statistical kriging model to interpolate and extrapolate the CO2 fluxes across the flight transects from the ground to the top of the boundary layer. Subsequently, using the results from these flights combined with the known emissions reported by the CEMS, we perform an inter-model comparison of alternative kriging methods to evaluate the performance of the kriging approach.
Atmospheric mercury emissions from mine wastes and surrounding geologically enriched terrains
Gustin, M.S.; Coolbaugh, M.F.; Engle, M.A.; Fitzgerald, B.C.; Keislar, R.E.; Lindberg, S.E.; Nacht, D.M.; Quashnick, J.; Rytuba, J.J.; Sladek, C.; Zhang, H.; Zehner, R.E.
2003-01-01
Waste rock and ore associated with Hg, precious and base metal mining, and their surrounding host rocks are typically enriched in mercury relative to natural background concentrations (<0.1 ??g Hg g-1). Mercury fluxes to the atmosphere from mineralized areas can range from background rates (0-15 ng m-2 h-1) to tens of thousands of ng m-2 h-1. Mercury enriched substrate constitutes a long-term source of mercury to the global atmospheric mercury pool. Mercury emissions from substrate are influenced by light, temperature, precipitation, and substrate mercury concentration, and occur during the day and night. Light-enhanced emissions are driven by two processes: desorption of elemental mercury accumulated at the soil:air interface, and photo reduction of mercury containing phases. To determine the need for and effectiveness of regulatory controls on short-lived anthropogenic point sources the contribution of mercury from geologic non-point sources to the atmospheric mercury pool needs to be quantified. The atmospheric mercury contribution from small areas of mining disturbance with relatively high mercury concentrations are, in general, less than that from surrounding large areas of low levels of mercury enrichment. In the arid to semi-arid west-ern United States volatilization is the primary means by which mercury is released from enriched sites.
Seitz, Wolfram; Winzenbacher, Rudi
2017-06-01
A comprehensive monitoring programme of trace organic chemicals (TOrC) was conducted for a German water protection area in karstic ground. The aim of this survey was to detect the potential anthropogenic influences of point sources such as wastewater treatment plants and diffuse pollution such as runoff water from roads on the raw water used for drinking water treatment. The programme comprised seven sampling campaigns within 2 years each with up to 20 sampling sites. In total, the programme included 84 anthropogenic compounds from pharmaceuticals, iodinated X-ray contrast media, sweeteners, industrial chemicals (benzotriazoles, melamines and benzothiazoles) and pesticide metabolites. Cyclamate occurred with the highest median concentration of 44 μg l -1 in untreated wastewater and acesulfame occurred with a concentration of 20 μg l -1 in treated wastewater. In runoff water from roads, the most relevant compounds were tolyltriazole with 2.3 μg l -1 and the desphenyl-chloridazon with 1.2 μg l -1 . In the stream waters, the highest median concentrations were found for melamine and acesulfame both at 0.61 μg l -1 . High elimination during conventional wastewater treatment was observed for 5 out of 49 compounds. These are acetyl-sulfamethoxazole, aciclovir, cyclamate, ibuprofen and saccharin. Based on the survey results, we propose a set of nine compounds to be used as indicators for wastewater, untreated wastewater and runoff water from roads for an efficient surveillance. The indicators are intended to detect anthropogenic influences in surface, ground and drinking water.
Analytical activities at the U.S. EPA regarding organic particulate matter
Fine aerosols are emitted from a wide variety of natural and anthropogenic sources. Anthropogenic aerosols exhibit detrimental effects on visibility, global climate, and human health and thus are of environmental concern. In turn, there is much interest in investigating the compl...
Rushdi, Ahmed I; Al-Zarban, Sheikha; Simoneit, Bernd R T
2006-09-01
Fine particles in the atmosphere from soil and sand resuspension contain a variety of organic compounds from natural biogenic and anthropogenic matter. Soil and sand samples from various sites near Kuwait city were collected, sieved to retain the fine particles, and extracted with a mixture of dichloromethane and methanol. The extracts were derivatized and analyzed by gas chromatography-mass spectrometry in order to characterize the chemical compositions and sources of the organic components. The major inputs of organic compounds were from both natural biogenic and anthropogenic sources in these samples. Vegetation was the major natural source of organic compounds and included n-alkanols, n-alkanoic acids, n-alkanes, sterols and triterpenoids. Saccharides had high concentrations (31-43%) in the sand dune and seafront samples, indicating sources from decomposed vegation materials and/or the presence of viable microbiota such as bacteria and fungi. Vehicular emission products, leakage of lubricating oils, discarded plastics and emissions from cooking operations were the major anthropogenic inputs in the samples from the urban areas. This input was mainly UCM, n-alkanes, hopanes, plasticizers and cholesterol, respectively.
Source-sector contributions to European ozone and fine PM in 2010 using AQMEII modeling data
NASA Astrophysics Data System (ADS)
Karamchandani, Prakash; Long, Yoann; Pirovano, Guido; Balzarini, Alessandra; Yarwood, Greg
2017-05-01
Source apportionment modeling provides valuable information on the contributions of different source sectors and/or source regions to ozone (O3) or fine particulate matter (PM2.5) concentrations. This information can be useful in designing air quality management strategies and in understanding the potential benefits of reducing emissions from a particular source category. The Comprehensive Air quality Model with Extensions (CAMx) offers unique source attribution tools, called the Ozone and Particulate Source Apportionment Technology (OSAT/PSAT), which track source contributions. We present results from a CAMx source attribution modeling study for a summer month and a winter month using a recently evaluated European CAMx modeling database developed for Phase 3 of the Air Quality Model Evaluation International Initiative (AQMEII). The contributions of several source sectors (including model boundary conditions of chemical species representing transport of emissions from outside the modeling domain as well as initial conditions of these species) to O3 or PM2.5 concentrations in Europe were calculated using OSAT and PSAT, respectively. A 1-week spin-up period was used to reduce the influence of initial conditions. Evaluation focused on 16 major cities and on identifying source sectors that contributed above 5 %. Boundary conditions have a large impact on summer and winter ozone in Europe and on summer PM2.5, but they are only a minor contributor to winter PM2.5. Biogenic emissions are important for summer ozone and PM2.5. The important anthropogenic sectors for summer ozone are transportation (both on-road and non-road), energy production and conversion, and industry. In two of the 16 cities, solvent and product also contributed above 5 % to summertime ozone. For summertime PM2.5, the important anthropogenic source sectors are energy, transportation, industry, and agriculture. Residential wood combustion is an important anthropogenic sector in winter for PM2.5 over most of Europe, with larger contributions in central and eastern Europe and the Nordic cities. Other anthropogenic sectors with large contributions to wintertime PM2.5 include energy, transportation, and agriculture.
Carotenuto, Federico; Gualtieri, Giovanni; Miglietta, Franco; Riccio, Angelo; Toscano, Piero; Wohlfahrt, Georg; Gioli, Beniamino
2018-02-22
CO 2 remains the greenhouse gas that contributes most to anthropogenic global warming, and the evaluation of its emissions is of major interest to both research and regulatory purposes. Emission inventories generally provide quite reliable estimates of CO 2 emissions. However, because of intrinsic uncertainties associated with these estimates, it is of great importance to validate emission inventories against independent estimates. This paper describes an integrated approach combining aircraft measurements and a puff dispersion modelling framework by considering a CO 2 industrial point source, located in Biganos, France. CO 2 density measurements were obtained by applying the mass balance method, while CO 2 emission estimates were derived by implementing the CALMET/CALPUFF model chain. For the latter, three meteorological initializations were used: (i) WRF-modelled outputs initialized by ECMWF reanalyses; (ii) WRF-modelled outputs initialized by CFSR reanalyses and (iii) local in situ observations. Governmental inventorial data were used as reference for all applications. The strengths and weaknesses of the different approaches and how they affect emission estimation uncertainty were investigated. The mass balance based on aircraft measurements was quite succesful in capturing the point source emission strength (at worst with a 16% bias), while the accuracy of the dispersion modelling, markedly when using ECMWF initialization through the WRF model, was only slightly lower (estimation with an 18% bias). The analysis will help in highlighting some methodological best practices that can be used as guidelines for future experiments.
NASA Astrophysics Data System (ADS)
Ryoo, S. B.; Moon, S. E.
1995-06-01
Modifications of surface air temperature caused by anthropogenic impacts have received much attention recently because of the heightened interest in climatic change. When an industrial area is constructed, resulting in a large-scale anthropogenic heat source, is it possible to detect the warming effect of the heat source? In this paper, the intensity of warming is estimated in the area of the source. A statistical model is suggested to estimate the warming caused by that anthropogenic heat source. The model used in this study is an accumulated intervention (AI) model that is applied to industrial heat perturbations that occurred in the area. To evaluate the AI model performance, the forecast experiment was carried out with an independent dataset. The data used in this study are the monthly mean temperatures at Pohang, Korea. The AI model was developed based on the data for the 38-year period from 1953 to 1990, and the forecast experiment was carried out with an independent dataset for the 2-year period from 1991 to 1992.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Skurikhin, Alexei N
With increasing deployment of satellite imaging systems, only a small fraction of collected data can be subject to expert scrutiny. We present and evaluate a two-tier approach to broad area search for signs of anthropogenic activities in high-resolution commercial satellite imagery. The method filters image information using semantically oriented interest points by combining Harris corner detection and spatial pyramid matching. The idea is that anthropogenic structures, such as rooftop outlines, fence corners, road junctions, are locally arranged in specific angular relations to each other. They are often oriented at approximately right angles to each other (which is known as rectilinearitymore » relation). Detecting the rectilinearity provides an opportunity to highlight regions most likely to contain anthropogenic activity. This is followed by supervised classification of regions surrounding the detected corner points as man-made vs. natural scenes. We consider, in particular, a search for anthropogenic activities in uncluttered areas. In this paper, we proposed and evaluated a two-tier approach to broad area search for signs of anthropogenic activities. Results from experiments on high-resolution ({approx}0.6m) commercial satellite image data showed the potential applicability of this approach and its ability of achieving both high precision and recall rates. The main advantage of combining corner-based cueing with general object recognition is that the incorporation of domain specific knowledge even in its more general form, such as presence of comers, provides a useful cue to narrow the focus of search for signs of anthropogenic activities. Combination of comer based cueing with spatial pyramid matching addressed the issue of comer categorization. An important practical issue for further research is optimizing the balance between false positive and false negative rates. While the results presented in the paper are encouraging, the problem of an automated broad area search for signs of anthropogenic activities remains challenging.« less
Spatial and temporal variability in desert dust and anthropogenic pollution in Iraq, 1997-2010.
Chudnovsky, A Alexandra; Koutrakis, Petros; Kostinski, Alex; Proctor, Susan P; Garshick, Eric
2017-01-01
Satellite imaging has emerged as a method for monitoring regional air pollution and detecting areas of high dust concentrations. Unlike ground observations, continuous data monitoring is available with global coverage of terrestrial and atmospheric components. In this study we test the utility of different sources of satellite data to assess air pollution concentrations in Iraq. SeaWiFS and MODIS Deep Blue (DB) aerosol optical depth (AOD) products were evaluated and used to characterize the spatial and temporal pollution levels from the late 1990s through 2010. The AOD and Ångström exponent (an indicator of particle size, since smaller Ångström exponent values reflect a source that includes larger particles) were correlated on 50 × 50 km spatial resolution. Generally, AOD and Ångström exponent were inversely correlated, suggesting a significant contribution of coarse particles from dust storms to AOD maxima. Although the majority of grid cells exhibited this trend, a weaker relationship in other locations suggested an additional contribution of fine particles from anthropogenic sources. Tropospheric NO 2 densities from the OMI satellite were elevated over cities, also consistent with a contribution from anthropogenic sources. Our analysis demonstrates the use of satellite imaging data to estimate relative pollution levels and source contributions in areas of the world where direct measurements are not available. The authors demonstrated how satellite data can be used to characterize exposures to dust and to anthropogenic pollution for future health related studies. This approach is of a great potential to investigate the associations between subject-specific exposures to different pollution sources and their health effects in inaccessible regions and areas where ground monitoring is unavailable.
Spatial and temporal variability in desert dust and anthropogenic pollution in Iraq, 1997–2010
Chudnovsky, A. Alexandra; Koutrakis, Petros; Kostinski, Alex; Proctor, Susan P.; Garshick, Eric
2016-01-01
Satellite imaging has emerged as a method for monitoring regional air pollution and detecting areas of high dust concentrations. Unlike ground observations, continuous data monitoring is available with global coverage of terrestrial and atmospheric components. In this study we test the utility of different sources of satellite data to assess air pollution concentrations in Iraq. SeaWiFS and MODIS Deep Blue (DB) aerosol optical depth (AOD) products were evaluated and used to characterize the spatial and temporal pollution levels from the late 1990s through 2010. The AOD and Ångström exponent (an indicator of particle size, since smaller Ångström exponent values reflect a source that includes larger particles) were correlated on 50 × 50 km spatial resolution. Generally, AOD and Ångström exponent were inversely correlated, suggesting a significant contribution of coarse particles from dust storms to AOD maxima. Although the majority of grid cells exhibited this trend, a weaker relationship in other locations suggested an additional contribution of fine particles from anthropogenic sources. Tropospheric NO2 densities from the OMI satellite were elevated over cities, also consistent with a contribution from anthropogenic sources. Our analysis demonstrates the use of satellite imaging data to estimate relative pollution levels and source contributions in areas of the world where direct measurements are not available. Implications The authors demonstrated how satellite data can be used to characterize exposures to dust and to anthropogenic pollution for future health related studies. This approach is of a great potential to investigate the associations between subject-specific exposures to different pollution sources and their health effects in inaccessible regions and areas where ground monitoring is unavailable. PMID:28001122
NASA Astrophysics Data System (ADS)
Makowski Giannoni, S.; Rollenbeck, R.; Trachte, K.; Bendix, J.
2014-10-01
Atmospheric sulfur deposition above certain limits can represent a threat to tropical forests, causing nutrient imbalances and mobilizing toxic elements that impact biodiversity and forest productivity. Atmospheric sources of sulfur deposited by precipitation have been roughly identified in only a few lowland tropical forests. Even scarcer are studies of this type in tropical mountain forests, many of them mega-diversity hotspots and especially vulnerable to acidic deposition. In these places, the topographic complexity and related streamflow conditions affect the origin, type, and intensity of deposition. Furthermore, in regions with a variety of natural and anthropogenic sulfur sources, like active volcanoes and biomass burning, no source emission data has been used for determining the contribution of each source to the deposition. The main goal of the current study is to evaluate sulfate (SO4- deposition by rain and occult precipitation at two topographic locations in a tropical mountain forest of southern Ecuador, and to trace back the deposition to possible emission sources applying back-trajectory modeling. To link upwind natural (volcanic) and anthropogenic (urban/industrial and biomass-burning) sulfur emissions and observed sulfate deposition, we employed state-of-the-art inventory and satellite data, including volcanic passive degassing as well. We conclude that biomass-burning sources generally dominate sulfate deposition at the evaluated sites. Minor sulfate transport occurs during the shifting of the predominant winds to the north and west. Occult precipitation sulfate deposition and likely rain sulfate deposition are mainly linked to biomass-burning emissions from the Amazon lowlands. Volcanic and anthropogenic emissions from the north and west contribute to occult precipitation sulfate deposition at the mountain crest Cerro del Consuelo meteorological station and to rain-deposited sulfate at the upriver mountain pass El Tiro meteorological station.
What We Can Say About the Roles of Natural and Anthropogenic Aerosols in Climate Change
NASA Astrophysics Data System (ADS)
Kahn, Ralph
2016-07-01
Although particles from natural sources dominate the globally averaged aerosol load, it is widely understood that human activity has added significantly to the atmospheric aerosol inventory in many regions. Anthropogenic contributions include pollution particles from industrial activity, transportation, cook-stoves, and other combustion sources, smoke from agricultural fires and those wildfires that result from land-management practices, soil and mineral dust mobilized in regions where overgrazing, severe tilling, or overuse of surface water resources have occurred, and biogenic particles from vegetation planted and maintained by the populance. The history of human influence is complex - in the 18th and 19th centuries agricultural burning tended to dominate the anthropogenic component in most places, whereas more recently, fossil fuel combustion leads the human contribution is many areas. However, identifying and quantifying the anthropogenic aerosol component on global scales is a challenging endeavor at present. Most estimates of the anthropogenic component come from aerosol transport models that are initialized with aerosol and precursor-gas source locations, emission strengths, and injection heights. The aerosol is then advected based on meteorological modeling, possibly modified chemically or physically, and removed by parameterized wet or dry deposition processes. Aerosol effects on clouds are also represented in some climate models, but with even greater uncertainty than the direct aerosol effects on Earth's radiation balance. Even for present conditions, aerosol source inventories are deduced from whatever constraints can be found, along with much creativity and many assumptions. Aerosol amount (i.e., aerosol optical depth) is routinely measured globally from space, but observational constraints on the anthropogenic component require some knowledge of the aerosol type as well, a much more difficult quantity to derive. As large-swath, multi-spectral, single-view instruments such as MODIS can provide some information about fine-mode vs. coarse-mode dominated aerosol over dark water, early efforts to constrain aerosol type assumed that some or all the fine-mode fraction is anthropogenic. However, this information is not sufficient to make the key anthropogenic vs. natural distinction in most places where the likely answer is not already known. Instruments providing more detailed measurements, such as multi-spectral, multi-angle and polarimetric imagers and multi-channel lidars, can offer tighter aerosol-type constraints in some circumstances, though generally not enough to specifically identify anthropogenic aerosols. The best we seem to be able to do with current data is to combine satellite and suborbital observations with models. And for the "pre-industrial" period, the analogy is usually made to the "natural" component of present-day aerosol, although there are ambiguities in our ability to distinguish natural from anthropogenic particles on regional-to-global scales, and the natural component itself might have changed over time. This talk will review where we stand, and what might be possible to say in the future.
A Compact, Low Resource Instrument to Measure Atmospheric Methane and Carbon Dioxide From Orbit
NASA Astrophysics Data System (ADS)
Rafkin, Scot; Davis, Michael; Varner, Ruth; Basu, Sourish; Bruhwiler, Lori; Luspay-Kuti, Adrienn; Mandt, Kathy; Roming, Pete; Soto, Alejandro; Tapley, Mark
2017-04-01
Methane is the second most important radiatively active trace gas forcing anthropogenic climate change. Methane has ˜28 times more warming potential than carbon dioxide on a 100-year time horizon, and the background atmospheric concentration of methane has increased by more than 150% compared to pre-industrial levels. The increase in methane abundance is driven by a combination of direct human activity, such as fossil fuel extraction and agriculture, and natural feedback processes that respond to human-induced climate change, such as increased wetland production. Accurate accounting of the exchange between the atmosphere and the natural and anthropogenic methane reservoirs is necessary to predict how methane concentration will increase going forward, how that increase will modulate the natural methane cycle, and how effective policy decisions might be at mitigating methane-induced climate change. Monitoring and quantifying methane source intensity and spatial-temporal variability has proven challenging; there are unresolved and scientifically significant discrepancies between flux estimates based on limited surface measurements (the so-called "bottom-up" method) and the values derived from limited, remotely-sensed estimates from orbit and modeling (the so-called "top-down" method). A major source of the discrepancy between bottom-up and top-down estimates is likely a result of insufficient accuracy and resolution of space-based instrumentation. Methane releases, especially anthropogenic sources, are often at kilometer-scale (or less), whereas past remote sensing instruments have at least an order of magnitude greater footprint areas. Natural sources may be larger in areal extent, but the enhancement over background levels can be just a few percent, which demands high spectral resolution and signal-to-noise ratios from monitoring instrumentation. In response to the need for higher performance space-based methane monitoring, we have developed a novel, compact, low-resource instrument that meets the accuracy and spatial resolution challenges demanded by methane exchange processes. The baseline instrument uses reflected sunlight 0.7591-0.7646 μm and 1.6058-1.6761 μm, permitting individual spectral identification of CH4, O2, CO2 and H2O. By combining spectral information, the complicating effects of aerosol and clouds can be reduced. A spectral resolving power of R˜20,000 is achieved by utilizing a novel matching off-axis parabolic (OAP) mirror system to send a collimated beam to an Echelle grating, which then picks off the high orders of interest and sends them back to one of the OAPs for final focus. A beamsplitter before the focus separates the near-visible O2 signal from the ˜1.6 μm CH4, CO2, and H2O signals, creating two separate imaging channels. A high-heritage H1RG detector is used in both channels. The instrument images a 0.03°× 5° field-of-view, with a point-source resolution of 0.03°. These specifications produce a 33 km wide instantaneous image at the nominal altitude of 380 km, with 200 m point-source resolution. Higher altitudes yield increased instantaneous coverage at the cost of wider point-source resolution. The 200 m pixels can be averaged to produce higher signal-to-noise while still maintaining km-scale resolution. The entire instrument consumes 55 W with a mass of 20 kg and total volume of 0.07 m3. Thus, the instrument provides performance similar to or better than existing hardware in a much smaller package. The small resource footprint provides the opportunity to fly as payload on one or multiple small satellite payloads or on the International Space Station.
Wang, Qi; Xie, Zhiyi; Li, Fangbai
2015-11-01
This study aims to identify and apportion multi-source and multi-phase heavy metal pollution from natural and anthropogenic inputs using ensemble models that include stochastic gradient boosting (SGB) and random forest (RF) in agricultural soils on the local scale. The heavy metal pollution sources were quantitatively assessed, and the results illustrated the suitability of the ensemble models for the assessment of multi-source and multi-phase heavy metal pollution in agricultural soils on the local scale. The results of SGB and RF consistently demonstrated that anthropogenic sources contributed the most to the concentrations of Pb and Cd in agricultural soils in the study region and that SGB performed better than RF. Copyright © 2015 Elsevier Ltd. All rights reserved.
Bindler, Richard
2011-08-01
Clair Patterson and colleagues demonstrated already four decades ago that the lead cycle was greatly altered on a global scale by humans. Moreover, this change occurred long before the implementation of monitoring programs designed to study lead and other trace metals. Patterson and colleagues also developed stable lead isotope analyses as a tool to differentiate between natural and pollution-derived lead. Since then, stable isotope analyses of sediment, peat, herbaria collections, soils, and forest plants have given us new insights into lead biogeochemical cycling in space and time. Three important conclusions from our studies of lead in the Swedish environment conducted over the past 15 years, which are well supported by extensive results from elsewhere in Europe and in North America, are: (1) lead deposition rates at sites removed from major point sources during the twentieth century were about 1,000 times higher than natural background deposition rates a few thousand years ago (~10 mg Pb m(-2) year(-1) vs. 0.01 mg Pb m(-2) year(-1)), and even today (~1 mg Pb m(-2) year(-1)) are still almost 100 times greater than natural rates. This increase from natural background to maximum fluxes is similar to estimated changes in body burdens of lead from ancient times to the twentieth century. (2) Stable lead isotopes ((206)Pb/(207)Pb ratios shown in this paper) are an effective tool to distinguish anthropogenic lead from the natural lead present in sediments, peat, and soils for both the majority of sites receiving diffuse inputs from long range and regional sources and for sites in close proximity to point sources. In sediments >3,500 years and in the parent soil material of the C-horizon, (206)Pb/(207)Pb ratios are higher, 1.3 to >2.0, whereas pollution sources and surface soils and peat have lower ratios that have been in the range 1.14-1.18. (3) Using stable lead isotopes, we have estimated that in southern Sweden the cumulative anthropogenic burden of atmospherically deposited lead is ~2-5 g Pb m(-2) and ~1 g Pb m(-2) in the "pristine" north. Half of this cumulative total was deposited before industrialization. (4) In the vicinity of the Rönnskär smelter in northern Sweden, a major point source during the twentieth century, there is an isotopic pattern that deviates from the general trends elsewhere, reflecting the particular history of ore usage at Rönnskär, which further demonstrates the chronological record of lead loading recorded in peat and in soil mor horizons.
NASA Technical Reports Server (NTRS)
Li, Can; Tsay, Si-Chee; Fu, Joshua S.; Dickerson, Russell R.; Ji, Qiang; Bell, Shaun W.; Gao, Yang; Zhang, Wu; Huang, Jianping; Li, Zhanqing;
2010-01-01
Trace gases and aerosols were measured in Zhangye (39.082degN, 100.276degE, 1460 m a.s. 1.), a rural site near the Gobi deserts in northwestern China during spring 2008. Primary trace gases (CO:265 ppb; SO2:3.4 ppb; NO(*y): 4.2 ppb; hereafter results given as means of hourly data) in the area were lower than in eastern China, but still indicative of marked anthropogenic emissions. Sizable aerosol mass concentration (153 micro-g/cu m) and light scattering (159/Mm at 500 nm) were largely attributable to dust emissions, and aerosol light absorption (10.3/Mm at 500 nm) was dominated by anthropogenic pollution. Distinct diurnal variations in meteorology and pollution were induced by the local valley terrain. Strong daytime northwest valley wind cleaned out pollution and was replaced by southeast mountain wind that allowed pollutants to build up overnight. In the afternoon, aerosols had single scattering albedo (SSA, 500 mn) of 0.95 and were mainly of supermicron particles, presumably dust, while at night smaller particles and SSA of 0.89-0.91 were related to Pollution. The diverse local emission sources were characterized: the CO/SO2, CO/NO(y), NO(y)/SO2 (by moles), and BC/CO (by mass) ratios for small point sources such as factories were 24.6-54.2, 25.8-35.9, 0.79-1.31, and 4.1-6.1 x 10(exp -3), respectively, compared to the corresponding inventory ratios of 43.7-71.9, 23.7-25.7, 1.84-2.79, and 3.4-4.0 x 10(exp -3) for the industrial sector in the area. The mixing between dust and pollution can be ubiquitous in this region. During a dust storm shown as an example, pollutants were observed to mix with dust, causing discernible changes in both SSA and aerosol size distribution. Further interaction between dust and pollutants during transport may modify the properties of dust particles that are critical for their large-scale impact on radiation, clouds, and global biogeochemical cycles.
Anthropogenic Radionuglides in Marine Polar Regions
NASA Astrophysics Data System (ADS)
Holm, Elis
The polar regions are important for the understanding of long range water and atmospheric transport of anthropogenic substances. Investigations show that atmospheric transport of anthropogenic radionuclides is the most important route of transport to the Antarctic while water transport plays a greater role for the Arctic. Fallout from nuclear detonation tests is the major source in the Antarctic while in the Arctic other sources, especially European reprocessing facilities, dominate for conservatively behaving rdionuclides such as 137Cs . The flux of 137Cs and 239+240Pu in the Antarctic is about 1/10 of that for the Arctic and the resulting concentrations in surface sea-water show the same ratio for the two areas. In the Antarctic concentration factors for 137Cs are higher than in the Arctic for similar species
NASA Astrophysics Data System (ADS)
Chong, Jihyo; Kim, Young J.; Baek, Jongho; Lee, Hanlim
2016-10-01
Major anthropogenic sources of sulphur dioxide in the troposphere include point sources such as power plants and combustion-derived industrial sources. Spatially resolved remote sensing of atmospheric trace gases is desirable for better estimation and validation of emission from those sources. It has been reported that Imaging Differential Optical Absorption Spectroscopy (I-DOAS) technique can provide the spatially resolved two-dimensional distribution measurement of atmospheric trace gases. This study presents the results of I-DOAS observations of SO2 from a large power plant. The stack plume from the Taean coal-fired power plant was remotely sensed with an I-DOAS instrument. The slant column density (SCD) of SO2 was derived by data analysis of the absorption spectra of the scattered sunlight measured by an I-DOAS over the power plant stacks. Two-dimensional distribution of SO2 SCD was obtained over the viewing window of the I-DOAS instrument. The measured SCDs were converted to mixing ratios in order to estimate the rate of SO2 emission from each stack. The maximum mixing ratio of SO2 was measured to be 28.1 ppm with a SCD value of 4.15×1017 molecules/cm2. Based on the exit velocity of the plume from the stack, the emission rate of SO2 was estimated to be 22.54 g/s. Remote sensing of SO2 with an I-DOAS instrument can be very useful for independent estimation and validation of the emission rates from major point sources as well as area sources.
Use of stable sulfur isotopes to identify sources of sulfate in Rocky Mountain snowpacks
Mast, M.A.; Turk, J.T.; Ingersoll, G.P.; Clow, D.W.; Kester, C.L.
2001-01-01
Stable sulfur isotope ratios and major ions in bulk snowpack samples were monitored at a network of 52 high-elevation sites along and near the Continental Divide from 1993 to 1999. This information was collected to better define atmospheric deposition to remote areas of the Rocky Mountains and to help identify the major source regions of sulfate in winter deposition. Average annual ??34S values at individual sites ranged from + 4.0 to + 8.2??? and standard deviations ranged from 0.4 to 1.6???. The chemical composition of all samples was extremely dilute and slightly acidic; average sulfate concentrations ranged from 2.4 to 12.2 ??eql-1 and pH ranged from 4.82 to 5.70. The range of ??34S values measured in this study indicated that snowpack sulfur in the Rocky Mountains is primarily derived from anthropogenic sources. A nearly linear relation between ??34S and latitude was observed for sites in New Mexico, Colorado, and southern Wyoming, which indicates that snowpack sulfate in the southern part of the network was derived from two isotopically distinct source regions. Because the major point sources of SO2 in the region are coal-fired powerplants, this pattern may reflect variations in the isotopic composition of coals burned by the plants. The geographic pattern in ??34S for sites farther to the north in Wyoming and Montana was much less distinct, perhaps rflecting the paucity of major point sources of SO2 in the northern part of the network.
Isotopic fingerprints of anthropogenic molybdenum in lake sediments.
Chappaz, Anthony; Lyons, Timothy W; Gordon, Gwyneth W; Anbar, Ariel D
2012-10-16
We measured the molybdenum isotope compositions (δ(98)Mo) of well-dated sediment cores from two lakes in eastern Canada in an effort to distinguish between natural and anthropogenic contributions to these freshwater aquatic systems. Previously, Chappaz et al. (1) ascribed pronounced 20th-century Mo concentration enrichments in these lakes to anthropogenic inputs. δ(98)Mo values in the deeper sediments (reflecting predominantly natural Mo sources) differ dramatically between the two lakes: -0.32 ± 0.17‰ for oxic Lake Tantare and +0.64 ± 0.09‰ for anoxic Lake Vose. Sediment layers previously identified as enriched in anthropogenic Mo, however, reveal significant δ(98)Mo shifts of ± 0.3‰, resulting in isotopically heavier values of +0.05 ± 0.18‰ in Lake Tantare and lighter values of +0.31 ± 0.03‰ in Lake Vose. We argue that anthropogenic Mo modifies the isotopic composition of the recent sediments, and we determine δ(98)Mo(anthropogenic) values of 0.1 ± 0.1‰ (Lake Vose) and 0.2 ± 0.2‰ (Lake Tantare). These calculated inputs are consistent with the δ(98)Mo of molybdenite (MoS(2)) likely delivered to the lakes via smelting of porphyry copper deposits (Lake Vose) or through combustion of coal and oil also containing Mo (Lake Tantare). Our results confirm the utility of Mo isotopes as a promising fingerprint of human impacts and perhaps the specific sources of contamination. Importantly, the magnitudes of the anthropogenic inputs are large enough, relative to the natural Mo cycles in each lake, to have an impact on the microbiological communities.
Anthropogenic- and natural sources of dust in peatland during the Anthropocene
NASA Astrophysics Data System (ADS)
Fiałkiewicz-Kozieł, B.; Smieja-Król, B.; Frontasyeva, M.; Słowiński, M.; Marcisz, K.; Lapshina, E.; Gilbert, D.; Buttler, A.; Jassey, V. E. J.; Kaliszan, K.; Laggoun-Défarge, F.; Kołaczek, P.; Lamentowicz, M.
2016-12-01
As human impact have been increasing strongly over the last decades, it is crucial to distinguish human-induced dust sources from natural ones in order to define the boundary of a newly proposed epoch - the Anthropocene. Here, we track anthropogenic signatures and natural geochemical anomalies in the Mukhrino peatland, Western Siberia. Human activity was recorded there from cal AD 1958 (±6). Anthropogenic spheroidal aluminosilicates clearly identify the beginning of industrial development and are proposed as a new indicator of the Anthropocene. In cal AD 1963 (±5), greatly elevated dust deposition and an increase in REE serve to show that the geochemistry of elements in the peat can be evidence of nuclear weapon testing; such constituted an enormous force blowing soil dust into the atmosphere. Among the natural dust sources, minor signals of dryness and of the Tunguska cosmic body (TCB) impact were noted. The TCB impact was indirectly confirmed by an unusual occurrence of mullite in the peat.
Anthropogenic- and natural sources of dust in peatland during the Anthropocene
Fiałkiewicz-Kozieł, B.; Smieja-Król, B.; Frontasyeva, M.; Słowiński, M.; Marcisz, K.; Lapshina, E.; Gilbert, D.; Buttler, A.; Jassey, V. E. J.; Kaliszan, K.; Laggoun-Défarge, F.; Kołaczek, P.; Lamentowicz, M.
2016-01-01
As human impact have been increasing strongly over the last decades, it is crucial to distinguish human-induced dust sources from natural ones in order to define the boundary of a newly proposed epoch - the Anthropocene. Here, we track anthropogenic signatures and natural geochemical anomalies in the Mukhrino peatland, Western Siberia. Human activity was recorded there from cal AD 1958 (±6). Anthropogenic spheroidal aluminosilicates clearly identify the beginning of industrial development and are proposed as a new indicator of the Anthropocene. In cal AD 1963 (±5), greatly elevated dust deposition and an increase in REE serve to show that the geochemistry of elements in the peat can be evidence of nuclear weapon testing; such constituted an enormous force blowing soil dust into the atmosphere. Among the natural dust sources, minor signals of dryness and of the Tunguska cosmic body (TCB) impact were noted. The TCB impact was indirectly confirmed by an unusual occurrence of mullite in the peat. PMID:27995953
Anthropogenic- and natural sources of dust in peatland during the Anthropocene.
Fiałkiewicz-Kozieł, B; Smieja-Król, B; Frontasyeva, M; Słowiński, M; Marcisz, K; Lapshina, E; Gilbert, D; Buttler, A; Jassey, V E J; Kaliszan, K; Laggoun-Défarge, F; Kołaczek, P; Lamentowicz, M
2016-12-20
As human impact have been increasing strongly over the last decades, it is crucial to distinguish human-induced dust sources from natural ones in order to define the boundary of a newly proposed epoch - the Anthropocene. Here, we track anthropogenic signatures and natural geochemical anomalies in the Mukhrino peatland, Western Siberia. Human activity was recorded there from cal AD 1958 (±6). Anthropogenic spheroidal aluminosilicates clearly identify the beginning of industrial development and are proposed as a new indicator of the Anthropocene. In cal AD 1963 (±5), greatly elevated dust deposition and an increase in REE serve to show that the geochemistry of elements in the peat can be evidence of nuclear weapon testing; such constituted an enormous force blowing soil dust into the atmosphere. Among the natural dust sources, minor signals of dryness and of the Tunguska cosmic body (TCB) impact were noted. The TCB impact was indirectly confirmed by an unusual occurrence of mullite in the peat.
Hogsden, Kristy L; Harding, Jon S
2012-03-01
We compared food web structure in 20 streams with either anthropogenic or natural sources of acidity and metals or circumneutral water chemistry in New Zealand. Community and diet analysis indicated that mining streams receiving anthropogenic inputs of acidic and metal-rich drainage had much simpler food webs (fewer species, shorter food chains, less links) than those in naturally acidic, naturally high metal, and circumneutral streams. Food webs of naturally high metal streams were structurally similar to those in mining streams, lacking fish predators and having few species. Whereas, webs in naturally acidic streams differed very little from those in circumneutral streams due to strong similarities in community composition and diets of secondary and top consumers. The combined negative effects of acidity and metals on stream food webs are clear. However, elevated metal concentrations, regardless of source, appear to play a more important role than acidity in driving food web structure. Copyright © 2011 Elsevier Ltd. All rights reserved.
Cong, Jinxin; Gao, Chuanyu; Zhang, Yan; Zhang, Shaoqing; He, Jiabao; Wang, Guoping
2016-02-24
Dating the start of intensive anthropogenic influence on ecosystems is important for identifying the conditions necessary for ecosystem recovery. However, few studies have focused on determining when anthropogenic influences on wetland began through sedimentary archives. To fill this critical gap in our knowledge, combustion sources and emission intensities, reconstructed via black carbon (BC) and polycyclic aromatic hydrocarbons (PAHs) were analyzed in two wetlands in the Sanjiang Plain in Northeast China. (14)C provided age control for the sedimentary records. By combining previous sedimentary and archaeological studies, we attempt to date the beginning of intensive anthropogenic influences on the Sanjiang Plain. Our results showed that BC deposition fluxes increased from 0.02 to 0.7 g C/m(2).yr during the last 10,000 years. An upward trend was apparent during the last 500 years. Before 1200 cal yr BP, human activities were minor, such that the wetland ecosystem in the Sanjiang Plain before this period may represent the reference conditions that for the recovery of these wetlands. As the human population increased after 1200 cal yr BP, combustion sources changed and residential areas became a major source of BC and PAHs. In this way, the wetland ecosystem gradually became more heavily influenced by human activities.
NASA Astrophysics Data System (ADS)
Cong, Jinxin; Gao, Chuanyu; Zhang, Yan; Zhang, Shaoqing; He, Jiabao; Wang, Guoping
2016-02-01
Dating the start of intensive anthropogenic influence on ecosystems is important for identifying the conditions necessary for ecosystem recovery. However, few studies have focused on determining when anthropogenic influences on wetland began through sedimentary archives. To fill this critical gap in our knowledge, combustion sources and emission intensities, reconstructed via black carbon (BC) and polycyclic aromatic hydrocarbons (PAHs) were analyzed in two wetlands in the Sanjiang Plain in Northeast China. 14C provided age control for the sedimentary records. By combining previous sedimentary and archaeological studies, we attempt to date the beginning of intensive anthropogenic influences on the Sanjiang Plain. Our results showed that BC deposition fluxes increased from 0.02 to 0.7 g C/m2.yr during the last 10,000 years. An upward trend was apparent during the last 500 years. Before 1200 cal yr BP, human activities were minor, such that the wetland ecosystem in the Sanjiang Plain before this period may represent the reference conditions that for the recovery of these wetlands. As the human population increased after 1200 cal yr BP, combustion sources changed and residential areas became a major source of BC and PAHs. In this way, the wetland ecosystem gradually became more heavily influenced by human activities.
Cong, Jinxin; Gao, Chuanyu; Zhang, Yan; Zhang, Shaoqing; He, Jiabao; Wang, Guoping
2016-01-01
Dating the start of intensive anthropogenic influence on ecosystems is important for identifying the conditions necessary for ecosystem recovery. However, few studies have focused on determining when anthropogenic influences on wetland began through sedimentary archives. To fill this critical gap in our knowledge, combustion sources and emission intensities, reconstructed via black carbon (BC) and polycyclic aromatic hydrocarbons (PAHs) were analyzed in two wetlands in the Sanjiang Plain in Northeast China. 14C provided age control for the sedimentary records. By combining previous sedimentary and archaeological studies, we attempt to date the beginning of intensive anthropogenic influences on the Sanjiang Plain. Our results showed that BC deposition fluxes increased from 0.02 to 0.7 g C/m2.yr during the last 10,000 years. An upward trend was apparent during the last 500 years. Before 1200 cal yr BP, human activities were minor, such that the wetland ecosystem in the Sanjiang Plain before this period may represent the reference conditions that for the recovery of these wetlands. As the human population increased after 1200 cal yr BP, combustion sources changed and residential areas became a major source of BC and PAHs. In this way, the wetland ecosystem gradually became more heavily influenced by human activities. PMID:26907560
Evaluating the climate benefits of CO2-enhanced oil recovery using life cycle analysis.
Cooney, Gregory; Littlefield, James; Marriott, Joe; Skone, Timothy J
2015-06-16
This study uses life cycle analysis (LCA) to evaluate the greenhouse gas (GHG) performance of carbon dioxide (CO2) enhanced oil recovery (EOR) systems. A detailed gate-to-gate LCA model of EOR was developed and incorporated into a cradle-to-grave boundary with a functional unit of 1 MJ of combusted gasoline. The cradle-to-grave model includes two sources of CO2: natural domes and anthropogenic (fossil power equipped with carbon capture). A critical parameter is the crude recovery ratio, which describes how much crude is recovered for a fixed amount of purchased CO2. When CO2 is sourced from a natural dome, increasing the crude recovery ratio decreases emissions, the opposite is true for anthropogenic CO2. When the CO2 is sourced from a power plant, the electricity coproduct is assumed to displace existing power. With anthropogenic CO2, increasing the crude recovery ratio reduces the amount of CO2 required, thereby reducing the amount of power displaced and the corresponding credit. Only the anthropogenic EOR cases result in emissions lower than conventionally produced crude. This is not specific to EOR, rather the fact that carbon-intensive electricity is being displaced with captured electricity, and the fuel produced from that system receives a credit for this displacement.
Armah, Frederick A; Obiri, Samuel; Yawson, David O; Onumah, Edward E; Yengoh, Genesis T; Afrifa, Ernest K A; Odoi, Justice O
2010-11-01
The levels of heavy metals in surface water and their potential origin (natural and anthropogenic) were respectively determined and analysed for the Obuasi mining area in Ghana. Using Hawth's tool an extension in ArcGIS 9.2 software, a total of 48 water sample points in Obuasi and its environs were randomly selected for study. The magnitude of As, Cu, Mn, Fe, Pb, Hg, Zn and Cd in surface water from the sampling sites were measured by flame Atomic Absorption Spectrophotometry (AAS). Water quality parameters including conductivity, pH, total dissolved solids and turbidity were also evaluated. Principal component analysis and cluster analysis, coupled with correlation coefficient analysis, were used to identify possible sources of these heavy metals. Pearson correlation coefficients among total metal concentrations and selected water properties showed a number of strong associations. The results indicate that apart from tap water, surface water in Obuasi has elevated heavy metal concentrations, especially Hg, Pb, As, Cu and Cd, which are above the Ghana Environmental Protection Agency (GEPA) and World Health Organisation (WHO) permissible levels; clearly demonstrating anthropogenic impact. The mean heavy metal concentrations in surface water divided by the corresponding background values of surface water in Obuasi decrease in the order of Cd > Cu > As > Pb > Hg > Zn > Mn > Fe. The results also showed that Cu, Mn, Cd and Fe are largely responsible for the variations in the data, explaining 72% of total variance; while Pb, As and Hg explain only 18.7% of total variance. Three main sources of these heavy metals were identified. As originates from nature (oxidation of sulphide minerals particularly arsenopyrite-FeAsS). Pb derives from water carrying drainage from towns and mine machinery maintenance yards. Cd, Zn, Fe and Mn mainly emanate from industry sources. Hg mainly originates from artisanal small-scale mining. It cannot be said that the difference in concentration of heavy metals might be attributed to difference in proximity to mining-related activities because this is inconsistent with the cluster analysis. Based on cluster analysis SN32, SN42 and SN43 all belong to group one and are spatially similar. But the maximum Cu concentration was found in SN32 while the minimum Cu concentration was found in SN42 and SN43.
Mustain, N.; Griggs, G.; Barnard, P.L.
2007-01-01
The beaches of the Santa Barbara Littoral Cell, which are narrow as a result of either natural and/or anthropogenic factors, may benefit from nourishment. Sand compatibility is fundamental to beach nourishment success and grain size is the parameter often used to evaluate equivalence. Only after understanding which sand sizes naturally compose beaches in a specific cell, especially the smallest size that remains on the beach, can the potential compatibility of source areas, such as offshore borrow sites, be accurately assessed. This study examines sediments on the beach and in the nearshore (5-20m depth) for the entire Santa Barbara Littoral Cell east of Point Conception. A digital bed sediment camera, the Eyeball??, and spatial autocorrelation technique were used to determine sediment grain size. Here we report on whether nearshore sediments are comparable and compatible with beach sands of the Santa Barbara Littoral Cell. ?? 2007 ASCE.
NASA Astrophysics Data System (ADS)
Domagalski, J. L.
2013-12-01
The SPARROW (Spatially Referenced Regressions On Watershed Attributes) model allows for the simulation of nutrient transport at un-gauged catchments on a regional scale. The model was used to understand natural and anthropogenic factors affecting phosphorus transport in developed, undeveloped, and mixed watersheds. The SPARROW model is a statistical tool that allows for mass balance calculation of constituent sources, transport, and aquatic decay based upon a calibration of a subset of stream networks, where concentrations and discharge have been measured. Calibration is accomplished using potential sources for a given year and may include fertilizer, geological background (based on bed-sediment samples and aggregated with geochemical map units), point source discharge, and land use categories. NHD Plus version 2 was used to model the hydrologic system. Land to water transport variables tested were precipitation, permeability, soil type, tile drains, and irrigation. For this study area, point sources, cultivated land, and geological background are significant phosphorus sources to streams. Precipitation and clay content of soil are significant land to water transport variables and various stream sizes show significance with respect to aquatic decay. Specific rock types result in different levels of phosphorus loading and watershed yield. Some important geological sources are volcanic rocks (andesite and basalt), granodiorite, glacial deposits, and Mesozoic to Cenozoic marine deposits. Marine sediments vary in their phosphorus content, but are responsible for some of the highest natural phosphorus yields, especially along the Central and Southern California coast. The Miocene Monterey Formation was found to be an especially important local source in southern California. In contrast, mixed metamorphic and igneous assemblages such as argillites, peridotite, and shales of the Trinity Mountains of northern California result in some of the lowest phosphorus yields. The agriculturally productive Central Valley of California has a low amount of background phosphorus in spite of inputs from streams draining upland areas. Many years of intensive agriculture may be responsible for the decrease of soil phosphorus in that area. Watersheds with significant background sources of phosphorus and large amounts of cultivated land had some of the highest per hectare yields. Seven different stream systems important for water management, or to describe transport processes, were investigated in detail for downstream changes in sources and loads. For example, the Klamath River (Oregon and California) has intensive agriculture and andesite-derived phosphorus in the upper reach. The proportion of agricultural-derived phosphorus decreases as the river flows into California before discharge to the ocean. The river flows through at least three different types of geological background sources from high to intermediate to very low. Knowledge of the role of natural sources in developed watersheds is critical for developing nutrient management strategies and these model results will have applicability for the establishment of realistic nutrient criteria.
NASA Astrophysics Data System (ADS)
Turner, A. J.; Jacob, D. J.; Wecht, K. J.; Maasakkers, J. D.; Lundgren, E.; Andrews, A. E.; Biraud, S. C.; Boesch, H.; Bowman, K. W.; Deutscher, N. M.; Dubey, M. K.; Griffith, D. W. T.; Hase, F.; Kuze, A.; Notholt, J.; Ohyama, H.; Parker, R.; Payne, V. H.; Sussmann, R.; Sweeney, C.; Velazco, V. A.; Warneke, T.; Wennberg, P. O.; Wunch, D.
2015-06-01
We use 2009-2011 space-borne methane observations from the Greenhouse Gases Observing SATellite (GOSAT) to estimate global and North American methane emissions with 4° × 5° and up to 50 km × 50 km spatial resolution, respectively. GEOS-Chem and GOSAT data are first evaluated with atmospheric methane observations from surface and tower networks (NOAA/ESRL, TCCON) and aircraft (NOAA/ESRL, HIPPO), using the GEOS-Chem chemical transport model as a platform to facilitate comparison of GOSAT with in situ data. This identifies a high-latitude bias between the GOSAT data and GEOS-Chem that we correct via quadratic regression. Our global adjoint-based inversion yields a total methane source of 539 Tg a-1 with some important regional corrections to the EDGARv4.2 inventory used as a prior. Results serve as dynamic boundary conditions for an analytical inversion of North American methane emissions using radial basis functions to achieve high resolution of large sources and provide error characterization. We infer a US anthropogenic methane source of 40.2-42.7 Tg a-1, as compared to 24.9-27.0 Tg a-1 in the EDGAR and EPA bottom-up inventories, and 30.0-44.5 Tg a-1 in recent inverse studies. Our estimate is supported by independent surface and aircraft data and by previous inverse studies for California. We find that the emissions are highest in the southern-central US, the Central Valley of California, and Florida wetlands; large isolated point sources such as the US Four Corners also contribute. Using prior information on source locations, we attribute 29-44 % of US anthropogenic methane emissions to livestock, 22-31 % to oil/gas, 20 % to landfills/wastewater, and 11-15 % to coal. Wetlands contribute an additional 9.0-10.1 Tg a-1.
Turner, A. J.; Jacob, D. J.; Wecht, K. J.; ...
2015-06-30
We use 2009–2011 space-borne methane observations from the Greenhouse Gases Observing SATellite (GOSAT) to estimate global and North American methane emissions with 4° × 5° and up to 50 km × 50 km spatial resolution, respectively. GEOS-Chem and GOSAT data are first evaluated with atmospheric methane observations from surface and tower networks (NOAA/ESRL, TCCON) and aircraft (NOAA/ESRL, HIPPO), using the GEOS-Chem chemical transport model as a platform to facilitate comparison of GOSAT with in situ data. This identifies a high-latitude bias between the GOSAT data and GEOS-Chem that we correct via quadratic regression. Our global adjoint-based inversion yields a totalmore » methane source of 539 Tg a −1 with some important regional corrections to the EDGARv4.2 inventory used as a prior. Results serve as dynamic boundary conditions for an analytical inversion of North American methane emissions using radial basis functions to achieve high resolution of large sources and provide error characterization. We infer a US anthropogenic methane source of 40.2–42.7 Tg a -1, as compared to 24.9–27.0 Tg a -1 in the EDGAR and EPA bottom-up inventories, and 30.0–44.5 Tg a -1 in recent inverse studies. Our estimate is supported by independent surface and aircraft data and by previous inverse studies for California. We find that the emissions are highest in the southern–central US, the Central Valley of California, and Florida wetlands; large isolated point sources such as the US Four Corners also contribute. Using prior information on source locations, we attribute 29–44 % of US anthropogenic methane emissions to livestock, 22–31 % to oil/gas, 20 % to landfills/wastewater, and 11–15 % to coal. Wetlands contribute an additional 9.0–10.1 Tg a -1.« less
Shikazono, N; Tatewaki, K; Mohiuddin, K M; Nakano, T; Zakir, H M
2012-01-01
Sediments of the Tamagawa River in central Japan were studied to explain the spatial variation, to identify the sources of heavy metals, and to evaluate the anthropogenic influence on these pollutants in the river. Sediment samples were collected from 20 sites along the river (five upstream, four midstream, and 11 downstream). Heavy metal concentrations, viz. chromium, nickel, copper, zinc, lead, cadmium, and molybdenum, in the samples were measured using inductively coupled plasma-mass spectroscopy. The chemical speciations of heavy metals in the sediments were identified by the widely used five-step Hall method. Lead isotopes were analyzed to identify what portion is contributed by anthropogenic sources. The total heavy metal concentrations were compared with global averages for continental crust (shale) and average values for Japanese river sediments. The mean heavy metal concentrations were higher in downstream sediments than in upstream and midstream samples, and the concentrations in the silt samples were higher than those in the sand samples. Speciation results demonstrate that, for chromium and nickel, the residual fractions were dominant. These findings imply that the influence of anthropogenic chromium and nickel contamination is negligible, while copper, zinc, and lead were mostly extracted in the non-residual fraction (metals in adsorbed/exchangeable/carbonate forms or bound to amorphous Fe oxyhydroxides, crystalline Fe oxides, or organic matter), indicating that these elements have high chemical mobility. The proportion of lead (Pb) isotopes in the downstream silt samples indicates that Pb accumulation is primarily derived from anthropogenic sources.
NASA Astrophysics Data System (ADS)
Sheng, Jian-Xiong; Jacob, Daniel J.; Turner, Alexander J.; Maasakkers, Joannes D.; Sulprizio, Melissa P.; Bloom, A. Anthony; Andrews, Arlyn E.; Wunch, Debra
2018-05-01
We use observations of boundary layer methane from the SEAC4RS aircraft campaign over the Southeast US in August-September 2013 to estimate methane emissions in that region through an inverse analysis with up to 0.25° × 0.3125° (25×25 km2) resolution and with full error characterization. The Southeast US is a major source region for methane including large contributions from oil and gas production and wetlands. Our inversion uses state-of-the-art emission inventories as prior estimates, including a gridded version of the anthropogenic EPA Greenhouse Gas Inventory and the mean of the WetCHARTs ensemble for wetlands. Inversion results are independently verified by comparison with surface (NOAA/ESRL) and column (TCCON) methane observations. Our posterior estimates for the Southeast US are 12.8 ± 0.9 Tg a-1 for anthropogenic sources (no significant change from the gridded EPA inventory) and 9.4 ± 0.8 Tg a-1 for wetlands (27 % decrease from the mean in the WetCHARTs ensemble). The largest source of error in the WetCHARTs wetlands ensemble is the land cover map specification of wetland areal extent. Our results support the accuracy of the EPA anthropogenic inventory on a regional scale but there are significant local discrepancies for oil and gas production fields, suggesting that emission factors are more variable than assumed in the EPA inventory.
Li, Li-Guan; Yin, Xiaole; Zhang, Tong
2018-05-24
Antimicrobial resistance (AMR) has been a worldwide public health concern. Current widespread AMR pollution has posed a big challenge in accurately disentangling source-sink relationship, which has been further confounded by point and non-point sources, as well as endogenous and exogenous cross-reactivity under complicated environmental conditions. Because of insufficient capability in identifying source-sink relationship within a quantitative framework, traditional antibiotic resistance gene (ARG) signatures-based source-tracking methods would hardly be a practical solution. By combining broad-spectrum ARG profiling with machine-learning classification SourceTracker, here we present a novel way to address the question in the era of high-throughput sequencing. Its potential in extensive application was firstly validated by 656 global-scale samples covering diverse environmental types (e.g., human/animal gut, wastewater, soil, ocean) and broad geographical regions (e.g., China, USA, Europe, Peru). Its potential and limitations in source prediction as well as effect of parameter adjustment were then rigorously evaluated by artificial configurations with representative source proportions. When applying SourceTracker in region-specific analysis, excellent performance was achieved by ARG profiles in two sample types with obvious different source compositions, i.e., influent and effluent of wastewater treatment plant. Two environmental metagenomic datasets of anthropogenic interference gradient further supported its potential in practical application. To complement general-profile-based source tracking in distinguishing continuous gradient pollution, a few generalist and specialist indicator ARGs across ecotypes were identified in this study. We demonstrated for the first time that the developed source-tracking platform when coupling with proper experiment design and efficient metagenomic analysis tools will have significant implications for assessing AMR pollution. Following predicted source contribution status, risk ranking of different sources in ARG dissemination will be possible, thereby paving the way for establishing priority in mitigating ARG spread and designing effective control strategies.
NASA Astrophysics Data System (ADS)
Burgos, Macarena; Ortega, Teodora; Bohórquez, Julio; Corzo, Alfonso; Rabouille, Christophe; Forja, Jesús M.
2018-01-01
Greenhouse gas production in coastal sediments is closely associated with the early diagenesis processes of organic matter and nutrients. Discharges from anthropogenic activities, particularly agriculture, fish farming and waste-water treatment plants supply large amounts of organic matter and inorganic nutrients that affect mineralization processes. Three coastal systems of Cadiz Bay (SW Spain) (Guadalete River, Rio San Pedro Creek and Sancti Petri Channel) were chosen to determine the seasonal variation of organic matter mineralization. Two sampling stations were selected in each system; one in the outer part, close to the bay, and another more inland, close to a discharge point of effluent related to anthropogenic activities. Seasonal variation revealed that metabolic reactions were driven by the annual change of temperature in the outer station of the systems. In contrast, these reactions depended on the amount of organic matter reaching the sediments in the outermost part of the systems, which was higher during winter. Oxygen is consumed in the first 0.5 cm indicating that suboxic and anoxic processes, such as denitrification, sulfate reduction and methanogenesis are important in these sediments. Sulfate reduction seems to account for most of the mineralization of organic matter at the marine stations, while methanogenesis is the main pathway at the sole freshwater station of this study, located inside the estuary of the Guadalete River, because of the lack of sulfate as electron acceptor. Results point to denitrification being the principal process of N2O formation. Diffusive fluxes varied between 2.6 and 160 mmol m-2 d-1 for dissolved inorganic carbon (DIC); 0.9 and 164.3 mmol m-2 d-1 for TA; 0.8 and 17.4 μmol m-2 d-1 for N2O; and 0.1 μmol and 13.1 mmol m-2 d-1 for CH4, indicating that these sediments act as a source of greenhouse gases to the water column.
Rochman, Chelsea M.; Tahir, Akbar; Williams, Susan L.; Baxa, Dolores V.; Lam, Rosalyn; Miller, Jeffrey T.; Teh, Foo-Ching; Werorilangi, Shinta; Teh, Swee J.
2015-01-01
The ubiquity of anthropogenic debris in hundreds of species of wildlife and the toxicity of chemicals associated with it has begun to raise concerns regarding the presence of anthropogenic debris in seafood. We assessed the presence of anthropogenic debris in fishes and shellfish on sale for human consumption. We sampled from markets in Makassar, Indonesia, and from California, USA. All fish and shellfish were identified to species where possible. Anthropogenic debris was extracted from the digestive tracts of fish and whole shellfish using a 10% KOH solution and quantified under a dissecting microscope. In Indonesia, anthropogenic debris was found in 28% of individual fish and in 55% of all species. Similarly, in the USA, anthropogenic debris was found in 25% of individual fish and in 67% of all species. Anthropogenic debris was also found in 33% of individual shellfish sampled. All of the anthropogenic debris recovered from fish in Indonesia was plastic, whereas anthropogenic debris recovered from fish in the USA was primarily fibers. Variations in debris types likely reflect different sources and waste management strategies between countries. We report some of the first findings of plastic debris in fishes directly sold for human consumption raising concerns regarding human health. PMID:26399762
Carbon dioxide (CO2) sequestration in deep saline aquifers and formations: Chapter 3
Rosenbauer, Robert J.; Thomas, Burt
2010-01-01
Carbon dioxide (CO2) capture and sequestration in geologic media is one among many emerging strategies to reduce atmospheric emissions of anthropogenic CO2. This chapter looks at the potential of deep saline aquifers – based on their capacity and close proximity to large point sources of CO2 – as repositories for the geologic sequestration of CO2. The petrochemical characteristics which impact on the suitability of saline aquifers for CO2 sequestration and the role of coupled geochemical transport models and numerical tools in evaluating site feasibility are also examined. The full-scale commercial CO2 sequestration project at Sleipner is described together with ongoing pilot and demonstration projects.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Matsui, H.; Koike, Makoto; Kondo, Yutaka
Organic aerosol (OA) simulations using the volatility basis-set approach were made for East Asia and its outflow region. Model simulations were evaluated through comparisons with OA measured by aerosol mass spectrometers in and around Tokyo (at Komaba and Kisai in summer 2003 and 2004) and over the outflow region in East Asia (at Fukue and Hedo in spring 2009). The simulations with aging processes of organic vapors reasonably well reproduced mass concentrations, temporal variations, and formation efficiency of observed OA at all sites. As OA mass was severely underestimated in the simulations without the aging processes, the oxidations of organicmore » vapors are essential for reasonable OA simulations over East Asia. By considering the aging processes, simulated OA concentrations considerably increased from 0.24 to 1.28 µg m-3 in the boundary layer over the whole of East Asia. OA formed from the interaction of anthropogenic and biogenic sources was also enhanced by the aging processes. The fraction of controllable OA was estimated to be 87 % of total OA over the whole of East Asia, showing that most of the OA in our simulations formed anthropogenically (controllable). A large portion of biogenic secondary OA (78 % of biogenic secondary OA) formed through the influence of anthropogenic sources. The high fraction of controllable OA in our simulations is likely because anthropogenic emissions are dominant over East Asia and OA formation is enhanced by anthropogenic sources and their aging processes. Both the amounts (from 0.18 to 1.12 µg m-3) and the fraction (from 75 % to 87 %) of controllable OA were increased by aging processes of organic vapors over East Asia.« less
Our fingerprint in tsunami deposits - anthropogenic markers as a new tsunami identification tool
NASA Astrophysics Data System (ADS)
Bellanova, P.; Schwarzbauer, J.; Reicherter, K. R.; Jaffe, B. E.; Szczucinski, W.
2016-12-01
Several recent geochemical studies have focused on the use of inorganic indicators to evaluate a tsunami origin of sediment in the geologic record. However, tsunami transport not only particulate sedimentary material from marine to terrestrial areas (and vice versa), but also associated organic material. Thus, tsunami deposits may be characterized by organic-geochemical parameters. Recently increased attention has been given to the use of natural organic substances (biomarkers) to identify tsunami deposits. To date no studies have been made investigating anthropogenic organic indicators in recent tsunami deposits. Anthropogenic organic markers are more sensitive and reliable markers compared to other tracers due to their specific molecular structural properties and higher source specificity. In this study we evaluate whether anthropogenic substances are useful indicators for determining whether an area has been inundated by a tsunami. We chose the Sendai Plain and Sanemoura and Oppa Bays, Japan, as study sites because the destruction of infrastructure by flooding released environmental pollutants (e.g., fuels, fats, tarmac, plastics, heavy metals, etc.) contaminating large areas of the coastal zone during the 2011 Tohoku-oki tsunami. Organic compounds from the tsunami deposits are extracted from tsunami sediment and compared with the organic signature of unaffected pre-tsunami samples using gas chromatography-mass spectrometry (GS/MS) based analyses. For the anthropogenic markers, compounds such as soil derived pesticides (DDT), source specific PAHs, halogenated aromatics from industrial sources were detected and used to observe the inland extent and the impact of the Tohoku-oki tsunami on the coastal region around Sendai.
Paini, Dean R.; Yemshanov, Denys
2012-01-01
Species can sometimes spread significant distances beyond their natural dispersal ability by anthropogenic means. International shipping routes and the transport of shipping containers, in particular are a commonly recognised pathway for the introduction of invasive species. Species can gain access to a shipping container and remain inside, hidden and undetected for long periods. Currently, government biosecurity agencies charged with intercepting and removing these invasive species when they arrive to a county’s border only assess the most immediate point of loading in evaluating a shipping container’s risk profile. However, an invasive species could have infested a container previous to this point and travelled undetected before arriving at the border. To assess arrival risk for an invasive species requires analysing the international shipping network in order to identify the most likely source countries and the domestic ports of entry where the species is likely to arrive. We analysed an international shipping network and generated pathway simulations using a first-order Markov chain model to identify possible source ports and countries for the arrival of Khapra beetle (Trogoderma granarium) to Australia. We found Kaohsiung (Taiwan) and Busan (Republic of Korea) to be the most likely sources for Khapra beetle arrival, while the port of Melbourne was the most likely point of entry to Australia. Sensitivity analysis revealed significant stability in the rankings of foreign and Australian ports. This methodology provides a reliable modelling tool to identify and rank possible sources for an invasive species that could arrive at some time in the future. Such model outputs can be used by biosecurity agencies concerned with inspecting incoming shipping containers and wishing to optimise their inspection protocols. PMID:22970258
The observed influence of local anthropogenic pollution on northern Alaskan cloud properties
DOE Office of Scientific and Technical Information (OSTI.GOV)
Maahn, Maximilian; de Boer, Gijs; Creamean, Jessie M.
Due to their importance for the radiation budget, liquid-containing clouds are a key component of the Arctic climate system. Depending on season, they can cool or warm the near-surface air. The radiative properties of these clouds depend strongly on cloud drop sizes, which are governed in part by the availability of cloud condensation nuclei. Here, we investigate how cloud drop sizes are modified in the presence of local emissions from industrial facilities at the North Slope of Alaska. For this, we use aircraft in situ observations of clouds and aerosols from the 5th Department of Energy Atmospheric Radiation Measurement (DOE ARM)more » Program's Airborne Carbon Measurements (ACME-V) campaign obtained in summer 2015. Comparison of observations from an area with petroleum extraction facilities (Oliktok Point) with data from a reference area relatively free of anthropogenic sources (Utqiaġvik/Barrow) represents an opportunity to quantify the impact of local industrial emissions on cloud properties. In the presence of local industrial emissions, the mean effective radii of cloud droplets are reduced from 12.2 to 9.4 µm, which leads to suppressed drizzle production and precipitation. At the same time, concentrations of refractory black carbon and condensation nuclei are enhanced below the clouds. These results demonstrate that the effects of anthropogenic pollution on local climate need to be considered when planning Arctic industrial infrastructure in a warming environment.« less
The observed influence of local anthropogenic pollution on northern Alaskan cloud properties
DOE Office of Scientific and Technical Information (OSTI.GOV)
Maahn, Maximilian; de Boer, Gijs; Creamean, Jessie M.
Due to their importance for the radiation budget, liquid-containing clouds are a key component of the Arctic climate system. Depending on season, they can cool or warm the near-surface air. The radiative properties of these clouds depend strongly on cloud drop sizes, which are governed in part by the availability of cloud condensation nuclei. Here, we investigate how cloud drop sizes are modified in the presence of local emissions from industrial facilities at the North Slope of Alaska. For this, we use aircraft in situ observations of clouds and aerosols from the 5th Department of Energy Atmospheric Radiation Measurement (DOE ARM)more » Program's Airborne Carbon Measurements (ACME-V) campaign obtained in summer 2015. Comparison of observations from an area with petroleum extraction facilities (Oliktok Point) with data from a reference area relatively free of anthropogenic sources (Utqiagvik/Barrow) represents an opportunity to quantify the impact of local industrial emissions on cloud properties. In the presence of local industrial emissions, the mean effective radii of cloud droplets are reduced from 12.2 to 9.4 µm, which leads to suppressed drizzle production and precipitation. At the same time, concentrations of refractory black carbon and condensation nuclei are enhanced below the clouds. These results demonstrate that the effects of anthropogenic pollution on local climate need to be considered when planning Arctic industrial infrastructure in a warming environment.« less
The observed influence of local anthropogenic pollution on northern Alaskan cloud properties
Maahn, Maximilian; de Boer, Gijs; Creamean, Jessie M.; ...
2017-12-11
Due to their importance for the radiation budget, liquid-containing clouds are a key component of the Arctic climate system. Depending on season, they can cool or warm the near-surface air. The radiative properties of these clouds depend strongly on cloud drop sizes, which are governed in part by the availability of cloud condensation nuclei. Here, we investigate how cloud drop sizes are modified in the presence of local emissions from industrial facilities at the North Slope of Alaska. For this, we use aircraft in situ observations of clouds and aerosols from the 5th Department of Energy Atmospheric Radiation Measurement (DOE ARM)more » Program's Airborne Carbon Measurements (ACME-V) campaign obtained in summer 2015. Comparison of observations from an area with petroleum extraction facilities (Oliktok Point) with data from a reference area relatively free of anthropogenic sources (Utqiagvik/Barrow) represents an opportunity to quantify the impact of local industrial emissions on cloud properties. In the presence of local industrial emissions, the mean effective radii of cloud droplets are reduced from 12.2 to 9.4 µm, which leads to suppressed drizzle production and precipitation. At the same time, concentrations of refractory black carbon and condensation nuclei are enhanced below the clouds. These results demonstrate that the effects of anthropogenic pollution on local climate need to be considered when planning Arctic industrial infrastructure in a warming environment.« less
Khazaei, Esmaeil; Milne-Home, William
2017-05-01
Elevated levels of chloride concentration due to anthropogenic activities including the road salts, septic effluent and agricultural sources are common in shallow groundwater of the recent glacial deposits north of Toronto, Ontario, Canada. Identifying suitable techniques for discriminating the source of the chloride concentration helps to better plan the protection of groundwater in the area. This paper examines the applicability of geochemical techniques with emphasis on Panno et al. (Ground Water 44: 176-187, 2006) and Mullaney et al. (2009) graphical approaches for discriminating the sources of chloride with known causes of impacts. The results indicated that the graphical methods developed using Cl - , Br - and/or total nitrogen (N) could identify the combined sources of road salts and septic systems. However, discriminating between the road salts, septic effluent or agricultural sources needs to be complemented by other techniques including the artificial sweeteners and isotope tracers.
Investigation of air pollution and regional climate change due to anthropogenic aerosols
NASA Astrophysics Data System (ADS)
Nakata, Makiko; Sano, Itaru; Mukai, Sonoyo
2016-10-01
Increased emissions of anthropogenic aerosols associated with economic growth can lead to increased concentrations of hazardous air pollutants. In particular, large cities in East Asia have experienced numerous heavy haze episodes. Atmospheric aerosol distributions in East Asia are complex, being influenced by both natural phenomena and human activity, with urban areas in particular being dominated by fine anthropogenic aerosols released from diesel-powered vehicles and industrial activity. In Japan, air pollution levels have been reduced; nevertheless, in recent years, there is increasing concern regarding air pollution caused by fine particulate matter. The origins of air pollution were examined, focusing on the comparison between aerosol properties observed from satellites and that on the ground. Because of their short life spans, concentrations of anthropogenic aerosols are highest over the source regions, and as a result, the climatic impacts of anthropogenic aerosols are also found to be most pronounced in these regions. In this study, aerosol impacts on climate are assessed by numerical model simulations. The direct effects of aerosols include reduced solar radiation, and hence a decrease in surface temperatures. In addition to these changes in the radiation budget, aerosols have a significant potential to change cloud and precipitation fields. These climatic responses to aerosols can manifest far from their source regions with high industrial activities.
Rushdi, Ahmed I; Al-Mutlaq, Khalid; Simoneit, Bernd R T
2005-11-01
Major advances have been made in molecular marker analysis to distinguish between natural and anthropogenic organic matter inputs to the atmosphere. Resuspension of soil and sand by wind is one of the major mechanisms that produces particle dusts in the atmosphere. Soil and sand samples from the Riyadh area were collected in winter 2002, sieved to remove coarse particles and extracted with a mixture of dichloromethane and methanol (3:1, v:v). The total extracts were analyzed by gas chromatography-mass spectrometry in order to characterize the contents and identify the potential sources of the organic components. The major organic compounds of these extracts were derived from natural biogenic and anthropogenic sources. Organic compounds from natural sources, mainly vegetation, were major in samples from outside the city of Riyadh and included n-alkanes, n-alkanoic acids, n- alkanols, methyl alkanoates, and sterols. Anthropogenic inputs were significant in the fine particles of soil and sand samples collected from populated areas of the city. They consisted mainly of n-alkanes, hopanes, UCM (from vehicular emissions), and plasticizers (from discarded plastics, e.g., shopping bags). Carbohydrates had high concentrations in all samples and indicate sources from decomposed cellulose fibers and/or the presence of viable microbiota such as bacteria and fungi.
Nitrate concentrations under irrigated agriculture
Zaporozec, A.
1983-01-01
In recent years, considerable interest has been expressed in the nitrate content of water supplies. The most notable toxic effect of nitrate is infant methemoglobinemia. The risk of this disease increases significantly at nitrate-nitrogen levels exceeding 10 mg/l. For this reason, this concentration has been established as a limit for drinking water in many countries. In natural waters, nitrate is a minor ionic constituent and seldom accounts for more than a few percent of the total anions. However, nitrate in a significant concentration may occur in the vicinity of some point sources such as septic tanks, manure pits, and waste-disposal sites. Non-point sources contributing to groundwater pollution are numerous and a majority of them are related to agricultural activities. The largest single anthropogenic input of nitrate into the groundwater is fertilizer. Even though it has not been proven that nitrogen fertilizers are responsible for much of nitrate pollution, they are generally recognized as the main threat to groundwater quality, especially when inefficiently applied to irrigated fields on sandy soils. The biggest challenge facing today's agriculture is to maintain the balance between the enhancement of crop productivity and the risk of groundwater pollution. ?? 1982 Springer-Verlag New York Inc.
NASA Astrophysics Data System (ADS)
Shetty, Suraj K.
Mercury (Hg) is a toxic pollutant and is important to understand its cycling in the environment. In this dissertation, a number of modeling investigations were conducted to better understand the emission from natural surfaces, the source-receptor relationship of the emissions, and emission reduction of atmospheric mercury. The first part of this work estimates mercury emissions from vegetation, soil and water surfaces using a number of natural emission processors and detailed (LAI) Leaf Area Index data from GIS (Geographic Information System) satellite products. East Asian domain was chosen as it contributes nearly 50% of the global anthropogenic mercury emissions into the atmosphere. The estimated annual natural mercury emissions (gaseous elemental mercury) in the domain are 834 Mg yr-1 with 462 Mg yr-1 contributing from China. Compared to anthropogenic sources, natural sources show greater seasonal variability (highest in simmer). The emissions are significant, sometimes dominant, contributors to total mercury emission in the regions. The estimates provide possible explanation for the gaps between the anthropogenic emission estimates based on activity data and the emission inferred from field observations in the regions. To understand the contribution of domestic emissions to mercury deposition in the United States, the second part of the work applies the mercury model of Community Multi-scale Air Quality Modeling system (CMAQ-Hg v4.6) to apportion the various emission sources attributing to the mercury wet and dry deposition in the 6 United States receptor regions. Contributions to mercury deposition from electric generating units (EGU), iron and steel industry (IRST), industrial point sources excluding EGU and IRST (OIPM), the remaining anthropogenic sources (RA), natural processes (NAT), and out-of-boundary transport (BC) in domain was estimated. The model results for 2005 compared reasonably well to field observations made by MDN (Mercury Deposition Network) and CAMNet (Canadian Atmospheric Mercury Measurement Network). The model estimated a total deposition of 474 Mg yr-1 to the CONUS (Contiguous United States) domain, with two-thirds being dry deposited. Reactive gaseous mercury contributed the most to 60% of deposition. Emission speciation distribution is a key factor for local deposition as contribution from large point sources can be as high as 75% near (< 100 km) the emission sources, indicating that emission reduction may result in direct deposition decrease near the source locations. Among the sources, BC contributes to about 68% to 91% of total deposition. Excluding the BC's contribution, EGU contributes to nearly 50% of deposition caused by CONUS emissions in the Northeast, Southeast and East Central regions, while emissions from natural processes are more important in the Pacific and West Central regions (contributing up to 40% of deposition). The modeling results implies that implementation of the new emission standards proposed by USEPA (United States Environmental Protection Agency) would significantly benefit regions that have larger contributions from EGU sources. Control of mercury emissions from coal combustion processes has attracted great attention due to its toxicity and the emission-control regulations and has lead to advancement in state-of-the-art control technologies that alleviate the impact of mercury on ecosystem and human health. This part of the work applies a sorption model to simulate adsorption of mercury in flue gases, onto a confined-bed of activated carbon. The model's performances were studied at various flue gas flow rates, inlet mercury concentrations and adsorption bed temperatures. The process simulated a flue gas, with inlet mercury concentration of 300 ppb, entering at a velocity of 0.3 m s-1 from the bottom into a fixed bed (inside bed diameter of 1 m and 3 m bed height; bed temperature of 25 °C) of activated carbon (particle size of 0.004 m with density of 0.5 g cm-3 and surface area of 90.25 cm2 g -1). The model result demonstrated that a batch of activated carbon bed was capable of controlling mercury emission for approximately 275 days after which further mercury uptake starts to decrease till it reaches about 500 days when additional control ceases. An increase in bed temperature significantly reduces mercury sorption capacity of the activated carbon. Increase in flue gas flow rate may result in faster consumption of sorption capacity initially but at a later stage, the sorption rate decreases due to reduced sorption capacity. Thus, overall sorption rate remains unaffected. The activated carbon's effective life (time to reach saturation) is not affected by inlet mercury concentration, implying that the designing and operation of a mercury sorption process can be done independently. The results provide quantitative indication for designing efficient confined-bed process to remove mercury from flue gases.
Implications of possible interpretations of "greenhouse gas balance" in the Paris Agreement
NASA Astrophysics Data System (ADS)
Millar, R.; Fuglestvedt, J. S.; Rogelj, J.; Allen, M. R.; Boucher, O.; Forster, P.; Kriegler, E.; Shindell, D. T.
2017-12-01
The main goal of the Paris Agreement as stated in its Article 2 is "Holding the increase in the global average temperature to well below 2°C above pre-industrial levels and pursuing efforts to limit the temperature increase to 1.5°C above pre-industrial levels…". Article 4 points to this long-term goal and the need to "… achieve balance between anthropogenic emissions by sources and removals by sinks of greenhouse gases …". The statement on "greenhouse gas balance" is subject to interpretation, and several clarifications are needed in order to make it operational for implementation in climate policies. Here we study possible interpretations from a scientific perspective and analyze their climatic implications. We clarify how the balance referred to in Article 4 of the Paris Agreement applies to anthropogenic sources and anthropogenic sinks and how the implications for individual gases depends strongly on the emission metrics used to relate them. We also show that the way in which balance is interpreted, achieved and maintained influences the anticipated temperature outcome over time. For example, achieving and maintaining net zero CO2-equivalent emissions calculated with the widely used metric Global Warming Potential with a horizon of 100 years (GWP100) - adopted for the implementation of the Kyoto Protocol and in UNFCCC reporting - would result in a peak and decline in global mean temperature. Adopting a different metric, like GWP* (Allen et al., 2016), would result in global mean temperatures remaining approximately constant once net zero CO2-equivalent emissions are achieved and maintained. Policymakers should be aware of these issues and choices and determine which approach is most appropriate in the context of the goals of the Paris Agreement.Reference:Allen, Fuglestvedt, Shine, Reisinger, Pierrehumbert, Forster: New use of global warming potentials to compare cumulative and short-lived climate pollutants. Nature Climate Change (2016). doi:10.1038/nclimate2998
Molecular structure impacts on secondary organic aerosol formation from glycol ethers
NASA Astrophysics Data System (ADS)
Li, Lijie; Cocker, David R.
2018-05-01
Glycol ethers, a class of widely used solvents in consumer products, are often considered exempt as volatile organic compounds based on their vapor pressure or boiling points by regulatory agencies. However, recent studies found that glycol ethers volatilize at ambient conditions nearly as rapidly as the traditional high-volatility solvents indicating the potential of glycol ethers to form secondary organic aerosol (SOA). This is the first work on SOA formation from glycol ethers. The impact of molecular structure, specifically -OH, on SOA formation from glycol ethers and related ethers are investigated in the work. Ethers with and without -OH, with methyl group hindrance on -OH and with -OH at different location are studied in the presence of NOX and under "NOX free" conditions. Photooxidation experiments under different oxidation conditions confirm that the processing of ethers is a combination of carbonyl formation, cyclization and fragmentation. Bulk SOA chemical composition analysis and oxidation products identified in both gas and particle phase suggests that the presence and location of -OH in the carbon bond of ethers determine the occurrence of cyclization mechanism during ether oxidation. The cyclization is proposed as a critical SOA formation mechanism to prevent the formation of volatile compounds from fragmentation during the oxidation of ethers. Glycol ethers with -CH2-O-CH2CH2OH structure is found to readily form cyclization products, especially with the presence of NOx, which is more relevant to urban atmospheric conditions than without NOx. Glycol ethers are evaluated as dominating SOA precursors among all ethers studied. It is estimated that the contribution of glycol ethers to anthropogenic SOA is roughly 1% of the current organic aerosol from mobile sources. The contribution of glycol ethers to anthropogenic SOA is roughly 1% of the current organic aerosol from mobile sources and will play a more important role in future anthropogenic SOA formation.
Srivastava, D; Favez, O; Bonnaire, N; Lucarelli, F; Haeffelin, M; Perraudin, E; Gros, V; Villenave, E; Albinet, A
2018-09-01
The present study aimed at performing PM 10 source apportionment, using positive matrix factorization (PMF), based on filter samples collected every 4h at a sub-urban station in the Paris region (France) during a PM pollution event in March 2015 (PM 10 >50μgm -3 for several consecutive days). The PMF model allowed to deconvolve 11 source factors. The use of specific primary and secondary organic molecular markers favoured the determination of common sources such as biomass burning and primary traffic emissions, as well as 2 specific biogenic SOA (marine+isoprene) and 3 anthropogenic SOA (nitro-PAHs+oxy-PAHs+phenolic compounds oxidation) factors. This study is probably the first one to report the use of methylnitrocatechol isomers as well as 1-nitropyrene to apportion secondary OA linked to biomass burning emissions and primary traffic emissions, respectively. Secondary organic carbon (SOC) fractions were found to account for 47% of the total OC. The use of organic molecular markers allowed the identification of 41% of the total SOC composed of anthropogenic SOA (namely, oxy-PAHs, nitro-PAHs and phenolic compounds oxidation, representing 15%, 9%, 11% of the total OC, respectively) and biogenic SOA (marine+isoprene) (6% in total). Results obtained also showed that 35% of the total SOC originated from anthropogenic sources and especially PAH SOA (oxy-PAHs+nitro-PAHs), accounting for 24% of the total SOC, highlighting its significant contribution in urban influenced environments. Anthropogenic SOA related to nitro-PAHs and phenolic compounds exhibited a clear diurnal pattern with high concentrations during the night indicating the prominent role of night-time chemistry but with different chemical processes involved. Copyright © 2018 Elsevier B.V. All rights reserved.
Krami, Loghman Khoda; Amiri, Fazel; Sefiyanian, Alireza; Shariff, Abdul Rashid B Mohamed; Tabatabaie, Tayebeh; Pradhan, Biswajeet
2013-12-01
One hundred and thirty composite soil samples were collected from Hamedan county, Iran to characterize the spatial distribution and trace the sources of heavy metals including As, Cd, Co, Cr, Cu, Ni, Pb, V, Zn, and Fe. The multivariate gap statistical analysis was used; for interrelation of spatial patterns of pollution, the disjunctive kriging and geoenrichment factor (EF(G)) techniques were applied. Heavy metals and soil properties were grouped using agglomerative hierarchical clustering and gap statistic. Principal component analysis was used for identification of the source of metals in a set of data. Geostatistics was used for the geospatial data processing. Based on the comparison between the original data and background values of the ten metals, the disjunctive kriging and EF(G) techniques were used to quantify their geospatial patterns and assess the contamination levels of the heavy metals. The spatial distribution map combined with the statistical analysis showed that the main source of Cr, Co, Ni, Zn, Pb, and V in group A land use (agriculture, rocky, and urban) was geogenic; the origin of As, Cd, and Cu was industrial and agricultural activities (anthropogenic sources). In group B land use (rangeland and orchards), the origin of metals (Cr, Co, Ni, Zn, and V) was mainly controlled by natural factors and As, Cd, Cu, and Pb had been added by organic factors. In group C land use (water), the origin of most heavy metals is natural without anthropogenic sources. The Cd and As pollution was relatively more serious in different land use. The EF(G) technique used confirmed the anthropogenic influence of heavy metal pollution. All metals showed concentrations substantially higher than their background values, suggesting anthropogenic pollution.
NASA Astrophysics Data System (ADS)
Makowski Giannoni, S.; Rollenbeck, R.; Trachte, K.; Bendix, J.
2014-05-01
Atmospheric sulfur deposition above certain limits can represent a threat to tropical forests, causing nutrient imbalances and mobilizing toxic elements that impact biodiversity and forest productivity. Atmospheric sources of sulfur deposited by precipitation have being roughly identified in only a few lowland tropical forests. Even scarcer are these type of studies in tropical mountain forests, many of them megadiversity hotspots and especially vulnerable to acidic deposition. Here, the topographic complexity and related streamflow condition the origin, type, and intensity of deposition. Furthermore, in regions with a variety of natural and anthropogenic sulfur sources, like active volcanoes and biomass-burning, no source-emission data has been used for determining the contribution of each of them to the deposition. The main goal of the current study is to evaluate sulfate (SO4-) deposition by rain and occult precipitation at two topographic locations in a tropical mountain forest of southern Ecuador, and to trace back the deposition to possible emission sources applying back trajectory modeling. To link upwind natural (volcanic) and anthropogenic (urban/industrial and biomass-burning) sulfur emissions and observed sulfate deposition, we employed state of the art inventory and satellite data, including volcanic passive degassing as well. We conclude that biomass-burning sources generally dominate sulfate deposition at the evaluated sites. Minor sulfate transport occurs during the shifting of the predominant winds to the north and west. Occult precipitation sulfate deposition and likely rain sulfate deposition are mainly linked to biomass-burning emissions from the Amazon lowlands. Volcanic and anthropogenic emissions from the north and west contribute to occult precipitation sulfate deposition at the mountain crest Cerro del Consuelo meteorological station and to rain-deposited sulfate at the upriver mountain-pass El Tiro meteorological station.
Rafiei, Behrouz; Ahmadi-Ghomi, Fatemeh; Karimkhani, Afshin
2017-08-15
Understanding the anthropogenic effects on the Sefidrud delta, the concentration of six metals (Cr, Co, Cu, Ni, Pb and Zn) was measured in two sites included the old Sefidrud delta (Amirabad, 23 samples) and the new Sefidrud delta (Kiashahr, 24 samples). Geoaccumulation Index (I geo ), Enrichment Factor (EF), Contamination Factor (CF) and Pollution Load Index (PLI) were used to determine the metal pollution in all sediment samples. Although the EF, I geo , CF and PLI results in the old delta indicate no significant pollution, sediment samples in the new delta show a considerable pollution. Since the sediment source and the lithology of the Sefidrud River drainage basin did not change in the past 500years, the metal pollution in the new delta must be from anthropogenic sources. Copyright © 2017 Elsevier Ltd. All rights reserved.
Global anthropogenic methane emissions 2005-2030: technical mitigation potentials and costs
NASA Astrophysics Data System (ADS)
Höglund-Isaksson, L.
2012-10-01
This paper presents estimates of current and future global anthropogenic methane emissions, their technical mitigation potential and associated costs for the period 2005 to 2030. The analysis uses the GAINS model framework to estimate emissions, mitigation potentials and costs for all major sources of anthropogenic methane for 83 countries/regions, which are aggregated to produce global estimates. Global emissions are estimated at 323 Mt methane in 2005, with an expected increase to 414 Mt methane in 2030. The technical mitigation potential is estimated at 195 Mt methane in 2030, whereof about 80 percent is found attainable at a marginal cost less than 20 Euro t-1 CO2eq when using a social planner cost perspective. With a private investor cost perspective, the corresponding fraction is only 30 percent. Major uncertainty sources in emission estimates are identified and discussed.
Two-step extraction method for lead isotope fractionation to reveal anthropogenic lead pollution.
Katahira, Kenshi; Moriwaki, Hiroshi; Kamura, Kazuo; Yamazaki, Hideo
2018-05-28
This study developed the 2-step extraction method which eluted the Pb adsorbing on the surface of sediments in the first solution by aqua regia and extracted the Pb absorbed inside particles into the second solution by mixed acid of nitric acid, hydrofluoric acid and hydrogen peroxide solution. We applied the method to sediments in the enclosed water area and found out that the isotope ratios of Pb in the second solution represented those of natural origin. This advantage of the method makes it possible to distinguish the Pb between natural origin and anthropogenic source on the basis of the isotope ratios. The results showed that the method was useful to discuss the Pb sources and that anthropogenic Pb in the sediment samples analysed was mainly derived from China because of transboundary air pollution.
Willis, John L; Al-Omari, Ahmed; Bastian, Robert; Brower, Bill; DeBarbadillo, Christine; Murthy, Sudhir; Peot, Christopher; Yuan, Zhiguo
2017-05-01
The impact of methanol (CH 3 OH) as a source of anthropogenic carbon dioxide (CO 2 ) in denitrification at wastewater treatment plants (WWTPs) has never been quantified. CH 3 OH is the most commonly purchased carbon source for sewage denitrification. Until recently, greenhouse gas (GHG) reporting protocols consistently ignored the liberation of anthropogenic CO 2 attributable to CH 3 OH. This oversight can likely be attributed to a simplifying notion that CO 2 produced through activated-sludge-process respiration is biogenic because most raw-sewage carbon is un-sequestered prior to entering a WWTP. Instead, a biogenic categorization cannot apply to fossil-fuel-derived carbon sources like CH 3 OH. This paper provides a summary of how CH 3 OH use at DC Water's Blue Plains Advanced Wastewater Treatment Plant (AWTP; Washington, DC, USA) amounts to 60 to 85% of the AWTP's Scope-1 emissions. The United States Environmental Protection Agency and Water Environment Federation databases suggest that CH 3 OH CO 2 likely represents one quarter of all Scope-1 GHG emissions attributable to sewage treatment in the USA. Finally, many alternatives to CH 3 OH use exist and are discussed.
Pun, Betty K; Wu, Shiang-Yuh; Seigneur, Christian
2002-08-15
As anthropogenic emissions of ozone (O3) precursors, fine particulate matter (PM2.5), and PM2.5 precursors continue to decrease in the United States, the fraction of O3 and PM2.5 attributable to natural sources may become significant in some locations, reducing the efficacy that can be expected from future controls of anthropogenic sources. Modeling studies were conducted to estimate the contribution of biogenic emissions to the formation of O3 and PM2.5 in Nashville/TN and the northeastern United States. Two approaches were used to bound the estimates. In an anthropogenic simulation, biogenic emissions and their influence at the domain boundaries were eliminated. Contributions of biogenic compounds to the simulated concentrations of O3 and PM2.5 were determined by the deviation of the concentrations in the anthropogenic case from those in the base case. A biogenic simulation was used to assess the amounts of O3 and PM2.5 produced in an environment free from anthropogenic influences in emissions and boundary conditions. In both locations, the contribution of biogenic emissions to O3 was small (<23%) on a domain-wide basis, despite significant biogenic volatile organic compounds (VOC) emissions (65-89% of total VOC emissions). However, the production of O3 was much more sensitive to biogenic emissions in urban areas (22-34%). Therefore, the effects of biogenic emissions on O3 manifested mostly via their interaction with anthropogenic emissions of NOx. In the anthropogenic simulations, the average contribution of biogenic and natural sources to PM2.5 was estimated at 9% in Nashville/TN and 12% in the northeast domain. Because of the long atmospheric lifetimes of PM2.5, the contribution of biogenic/natural PM2.5 from the boundary conditions was higher than the contribution of biogenic aerosols produced within the domain. The elimination of biogenic emissions also affected the chemistry of other secondary PM2.5 components. Very little PM2.5 was formed in the biogenic simulations.
Jadoon, Waqar Azeem; Khpalwak, Wahdatullah; Chidya, Russel Chrispine Garven; Abdel-Dayem, Sherif Mohamed Mohamed Ali; Takeda, Kazuhiko; Makhdoom, Masood Arshad; Sakugawa, Hiroshi
2018-01-01
This study was designed to investigate selected road-dust associated heavy metals, their relations with natural and anthropogenic sources, and potential human and environmental health risks. For this purpose, 42 and 36 road-dusts samples were collected from Jalalabad and Kabul cities (Afghanistan), respectively. The following elements were found in descending concentrations: Mn, Zn, Pb, Ni, Cu, Cr, Co, and Cd in Jalalabad; and Mn, Zn, Ni, Cu, Cr, Pb, Co, and Cd in Kabul. Except for Ni, all the elemental contents were less than the Canadian permissible limits in residential/parkland soils. Principle Component Analysis and enrichment of Cd, Cu, Ni, Pb, and Zn pointed to anthropogenic sources, whereas Co, Cr, and Mn indicated crustal inputs. Broadly, Cd monomial risk index ([Formula: see text]) was considerable; however, one site each in both cities showed high risk ([Formula: see text] ≥ 350). The potential ecological risk (RI) is mostly low; however, at some sites, the risk was considerable. Ingestion appeared to be the main exposure route (99%) for heavy metals and contributed > 90% to noncancerous (all residents), as well as 92% (children) and 75-89% (adults) cancerous risks. The noncancerous risks of all metals and their integrated risks for all residents were within acceptable levels. Moreover, potential cancer risks in children from Ni and Cr were slightly higher than the US-EPA safe levels but were within acceptable levels for adults. This study found higher risks to children and therefore recommends proper management and ways to control metals pollution load in these areas to decrease human health and RIs.
NASA Astrophysics Data System (ADS)
Ren, Y.
2017-12-01
Context Land surface temperatures (LSTs) spatio-temporal distribution pattern of urban forests are influenced by many ecological factors; the identification of interaction between these factors can improve simulations and predictions of spatial patterns of urban cold islands. This quantitative research requires an integrated method that combines multiple sources data with spatial statistical analysis. Objectives The purpose of this study was to clarify urban forest LST influence interaction between anthropogenic activities and multiple ecological factors using cluster analysis of hot and cold spots and Geogdetector model. We introduced the hypothesis that anthropogenic activity interacts with certain ecological factors, and their combination influences urban forests LST. We also assumed that spatio-temporal distributions of urban forest LST should be similar to those of ecological factors and can be represented quantitatively. Methods We used Jinjiang as a representative city in China as a case study. Population density was employed to represent anthropogenic activity. We built up a multi-source data (forest inventory, digital elevation models (DEM), population, and remote sensing imagery) on a unified urban scale to support urban forest LST influence interaction research. Through a combination of spatial statistical analysis results, multi-source spatial data, and Geogdetector model, the interaction mechanisms of urban forest LST were revealed. Results Although different ecological factors have different influences on forest LST, in two periods with different hot spots and cold spots, the patch area and dominant tree species were the main factors contributing to LST clustering in urban forests. The interaction between anthropogenic activity and multiple ecological factors increased LST in urban forest stands, linearly and nonlinearly. Strong interactions between elevation and dominant species were generally observed and were prevalent in either hot or cold spots areas in different years. Conclusions In conclusion, a combination of spatial statistics and GeogDetector models should be effective for quantitatively evaluating interactive relationships among ecological factors, anthropogenic activity and LST.
Anthropogenic CO2 emissions from a megacity in the Yangtze River Delta of China.
Hu, Cheng; Liu, Shoudong; Wang, Yongwei; Zhang, Mi; Xiao, Wei; Wang, Wei; Xu, Jiaping
2018-06-03
Anthropogenic CO 2 emissions from cities represent a major source contributing to the global atmospheric CO 2 burden. Here, we examined the enhancement of atmospheric CO 2 mixing ratios by anthropogenic emissions within the Yangtze River Delta (YRD), China, one of the world's most densely populated regions (population greater than 150 million). Tower measurements of CO 2 mixing ratios were conducted from March 2013 to August 2015 and were combined with numerical source footprint modeling to help constrain the anthropogenic CO 2 emissions. We simulated the CO 2 enhancements (i.e., fluctuations superimposed on background values) for winter season (December, January, and February). Overall, we observed mean diurnal variation of CO 2 enhancement of 23.5~49.7 μmol mol -1 , 21.4~52.4 μmol mol -1 , 28.1~55.4 μmol mol -1 , and 29.5~42.4 μmol mol -1 in spring, summer, autumn, and winter, respectively. These enhancements were much larger than previously reported values for other countries. The diurnal CO 2 enhancements reported here showed strong similarity for all 3 years of the study. Results from source footprint modeling indicated that our tower observations adequately represent emissions from the broader YRD area. Here, the east of Anhui and the west of Jiangsu province contributed significantly more to the anthropogenic CO 2 enhancement compared to the other sectors of YRD. The average anthropogenic CO 2 emission in 2014 was 0.162 (± 0.005) mg m -2 s -1 and was 7 ± 3% higher than 2010 for the YRD. Overall, our emission estimates were significantly smaller (9.5%) than those estimated (0.179 mg m -2 s -1 ) from the EDGAR emission database.
Cruise ships as a source of avian mortality during fall migration
Bocetti, Carol I.
2011-01-01
Avian mortality during fall migration has been studied at many anthropogenic structures, most of which share the common feature of bright lighting. An additional, unstudied source of avian mortality during fall migration is recreational cruise ships that are brightly lit throughout the night. I documented a single mortality event of eight Common Yellowthroats (Geothlypis trichas) on one ship during part of one night in fall 2003, but suggest this is a more wide-spread phenomenon. The advertised number of ship-nights for 50 cruise ships in the Caribbean Sea during fall migration in 2003 was 2,981. This may pose a significant, additional, anthropogenic source of mortality that warrants further investigation, particularly because impacts could be minimized if this source of avian mortality is recognized. ?? 2011 by the Wilson Ornithological Society.
Rezza, Carmela; Albanese, Stefano; Ayuso, Robert A.; Lima, Annamaria; Sorvari, Jaana; De Vivo, Benedetto
2018-01-01
A geochemical survey was carried out to investigate metal contamination in the Domizio Littoral and Agro Aversano area (Southern Italy) by means of soil, groundwater, human hair and corn samples. Pb isotope ratios were also determined to identify the sources of metals. Specifically, the investigation focused on topsoils (n = 1064), groundwater (n = 26), 25 human hair (n = 24) and corn samples (n = 13). Topsoils have been sampled and analysed in a previous study for 53 elements (including potentially harmful ones), and determined by ICP-MS after dissolving with aqua regia. Groundwater was analysed for 72 elements by ICP-MS and by ICP-ES. Samples of human hair were prepared and analysed for 16 elements by ICP-MS. Dried corn collected at several farms were also analysed for 53 elements by ICP-MS. The isotopic ratios of 206Pb/207Pb and 208Pb/207Pb in selected topsoil (n = 24), groundwater (n = 9), human hair (n = 9) and corn (n = 4) samples were analysed from both eluates and residues to investigate possible anthropogenic contamination and geogenic contributions. All data were processed and mapped by ArcGis software to produce interpolated maps and contamination factor maps of potentially harmful elements, in accordance with Italian Environmental Law (Legislative Decree 152/06). Results show that soil sampling sites are characterized by As, Cd, Co, Cr, Cu, Hg, Pb, Se, and Zn contents exceeding the action limits established for residential land use (RAL) and, in some cases, also the action limits for industrial land use (IAL) as established by Legislative Decree 152/06. A map of contamination factors and a map showing the degrees of contamination indicate that the areas in the municipalities of Acerra, Casoria and Giugliano have been affected by considerable anthropogenic-related pollution. To interpret the isotopic data and roughly estimate proportion of Pb from an anthropogenic source we broadly defined possible natural and anthropogenic Pb end-member fields based on literature data. For example, we summarized data for Vesuvius and Campi Flegrei volcanic rocks, gasoline, and aerosol deposits.Lead isotope data show mixing between geogenic and anthropogenic sources. Topsoil, groundwater, human hair and corn samples show a greater contribution from geogenic sources like the Yellow Tuff (from Campi Flegrei) and volcanic rocks from Mt. Vesuvius. Aerosols, fly ash and gasoline (anthropogenic sources) have also been contributors. In detail, 46% of the topsoil residues, 96% of topsoil leachates, 88% of groundwater, 90% of human hair, and 25% of corn samples indicate that > 50% percent of the lead in this area can be ascribed to anthropogenic activity.
Understanding Biogenic and Anthropogenic Trace Gas Variations Measured Near Cool, CA in June 2010
NASA Astrophysics Data System (ADS)
Klein, B. Z.; Flowers, B. A.; Gorkowski, K.; Dubey, M. K.; Knighton, W. B.; Floerchinger, C.; Herndon, S. C.; Fast, J. D.; Zaveri, R. A.
2011-12-01
Trace gas signatures produced by forested and urban areas differ greatly. Forested areas are dominated by gases produced during photosynthesis and respiration: CO2 and volatile organic compounds (VOCs) including terpenes and isoprene. Urban areas are heavily influenced by vehicle exhaust emissions and have elevated levels of CO, NOx and aromatic hydrocarbons such as benzene. Ozone is produced as a byproduct of both of these sources; it is produced when NOx from urban areas reacts with either anthropogenic or biogenic hydrocarbons. The Carbonaceous Aerosol and Radiative Effects Study (CARES) campaign was conducted during June 2010, in part to observe the evolution of urban air masses as they mix into rural locations and to better understand anthropogenic-biogenic photochemical interactions. The campaign included two ground-based sampling sites, one in Sacramento, CA (T0) and one downwind, approximately 70km NE, rurally located near Cool, CA (T1). In situ measurements of CO2, CO, O3, NO and multiple different VOCs were performed at the T1 site during the study, and are analyzed here to gain insights into the chemistry and transport of these trace gases. Comparisons between these trace gases coupled with transport modeling is used to delineate biogenic and anthropogenic sources. Additionally, comparisons between trace gases produced predominately by biogenic sources provide valuable information on how meteorology affects their production. Two atmospheric models (HYSPLIT back-trajectories and WRF forecasts) are used to predict transport episodes, where polluted air masses from the Sacramento or more distant San Francisco areas are transported to Cool. The two models display significant overlap for eleven different transport episodes during the study period. Both models also agree on two transport-free multiple-day periods. By examining the periods during which the models are in agreement, we are able to characterize with high certainty the trace gas signatures of local biogenic sources and also the significance of short-range transported anthropogenic trace gases.
Anthropogenic Sulphur Dioxide Load over China as Observed from Different Satellite Sensors
NASA Technical Reports Server (NTRS)
Koukouli, M. E.; Balis, D. S.; Johannes Van Der A, Ronald; Theys, N.; Hedelt, P.; Richter, A.; Krotkov, N.; Li, Can; Taylor, M.
2016-01-01
China, with its rapid economic growth and immense exporting power, has been the focus of many studies during this previous decade quantifying its increasing emissions contribution to the Earth's atmosphere. With a population slowly shifting towards enlarged power and purchasing needs, the ceaseless inauguration of new power plants, smelters, refineries and industrial parks leads infallibly to increases in sulphur dioxide, SO2, emissions. The recent capability of next generation algorithms as well as new space-borne instruments to detect anthropogenic SO2 loads has enabled a fast advancement in this field. In the following work, algorithms providing total SO2 columns over China based on SCIAMACHY/Envisat, OMI/Aura and GOME2/MetopA observations are presented. The need for post-processing and gridding of the SO2 fields is further revealed in this work, following the path of previous publications. Further, it is demonstrated that the usage of appropriate statistical tools permits studying parts of the datasets typically excluded, such as the winter months loads. Focusing on actual point sources, such as megacities and known power plant locations, instead of entire provinces, monthly mean time series have been examined in detail. The sharp decline in SO2 emissions in more than 90% - 95% of the locations studied confirms the recent implementation of government desulphurisation legislation; however, locations with increases, even for the previous five years, are also identified. These belong to provinces with emerging economies which are in haste to install power plants and are possibly viewed leniently by the authorities, in favour of growth. The SO2 load seasonality has also been examined in detail with a novel mathematical tool, with 70% of the point sources having a statistically significant annual cycle with highs in winter and lows in summer, following the heating requirements of the Chinese population.
Anthropogenic sulphur dioxide load over China as observed from different satellite sensors
NASA Astrophysics Data System (ADS)
Koukouli, M. E.; Balis, D. S.; van der A, Ronald Johannes; Theys, N.; Hedelt, P.; Richter, A.; Krotkov, N.; Li, C.; Taylor, M.
2016-11-01
China, with its rapid economic growth and immense exporting power, has been the focus of many studies during this previous decade quantifying its increasing emissions contribution to the Earth's atmosphere. With a population slowly shifting towards enlarged power and purchasing needs, the ceaseless inauguration of new power plants, smelters, refineries and industrial parks leads infallibly to increases in sulphur dioxide, SO2, emissions. The recent capability of next generation algorithms as well as new space-borne instruments to detect anthropogenic SO2 loads has enabled a fast advancement in this field. In the following work, algorithms providing total SO2 columns over China based on SCIAMACHY/Envisat, OMI/Aura and GOME2/MetopA observations are presented. The need for post-processing and gridding of the SO2 fields is further revealed in this work, following the path of previous publications. Further, it is demonstrated that the usage of appropriate statistical tools permits studying parts of the datasets typically excluded, such as the winter months loads. Focusing on actual point sources, such as megacities and known power plant locations, instead of entire provinces, monthly mean time series have been examined in detail. The sharp decline in SO2 emissions in more than 90%-95% of the locations studied confirms the recent implementation of government desulphurisation legislation; however, locations with increases, even for the previous five years, are also identified. These belong to provinces with emerging economies which are in haste to install power plants and are possibly viewed leniently by the authorities, in favour of growth. The SO2 load seasonality has also been examined in detail with a novel mathematical tool, with 70% of the point sources having a statistically significant annual cycle with highs in winter and lows in summer, following the heating requirements of the Chinese population.
Anthropogenic land uses elevate metal levels in stream water in an urbanizing watershed.
Yu, Shen; Wu, Qian; Li, Qingliang; Gao, Jinbo; Lin, Qiaoying; Ma, Jun; Xu, Qiufang; Wu, Shengchun
2014-08-01
Land use/cover change is a dominant factor affecting surface water quality in rapidly developing areas of Asia. In this study we examined relationships between land use and instream metal loadings in a rapidly developing mixed land use watershed in southeastern China. Five developing subwatersheds and one forested reference site (head water) were instrumented with timing- and rainfall-triggered autosampler and instream loadings of anthropogenic metals (Cu, Zn, Pb, Cr, Cd, and Mn) were monitored from March 2012 to December 2013. Farm land and urban land were positively, and forest and green land were negatively associated with metal loadings (except Cr) in stream water. All developing sites had higher loadings than the reference head water site. Assessed by Chinese surface water quality standard (GB3830-2002), instream loadings of Cu and Zn occasionally exceeded the Class I thresholds at monitoring points within farmland dominated subwatersheds while Mn loadings were greater than the limit for drinking water sources at all monitoring points. Farm land use highly and positively contributed to statistical models of instream loadings of Cu, Zn, Cd, and Mn while urban land use was the dominant contributor to models of Pb and Cd loadings. Rainfall played a crucial role in metal loadings in stream water as a direct source (there were significant levels of Cu and Zn in rain water) and as a driver of watershed processes (loadings were higher in wet years and seasons). Urbanization effects on metal loadings in this watershed are likely to change rapidly with development in future years. Further monitoring to characterize these changes is clearly warranted and should help to develop plans to avoid conflicts between economic development and water quality degradation in this watershed and in watersheds throughout rapidly developing areas of Asia. Copyright © 2014 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Earl, Nick; Simmonds, Ian; Tapper, Nigel
2015-11-01
One approach to quantifying anthropogenic influences on the environment and the consequences of those is to examine weekly cycles (WCs). No long-term natural process occurs on a WC so any such signal can be considered anthropogenic. There is much ongoing scientific debate as to whether regional-scale WCs exist above the statistical noise level, with most significant studies claiming that anthropogenic aerosols and their interaction with solar radiation and clouds (direct/indirect effect) is the controlling factor. A major source of anthropogenic aerosol, underrepresented in the literature, is active fire (AF) from anthropogenic burning for land clearance/management. WCs in AF have not been analyzed heretofore, and these can provide a mechanism for observed regional-scale WCs in several meteorological variables. We show that WCs in AFs are highly pronounced for many parts of the world, strongly influenced by the working week and particularly the day(s) of rest, associated with religious practices.
Stable nitrogen isotopes in coastal macroalgae: geographic and anthropogenic variability.
Viana, Inés G; Bode, Antonio
2013-01-15
Growing human population adds to the natural nitrogen loads to coastal waters. Both anthropogenic and natural nitrogen is readily incorporated in new biomass, and these different nitrogen sources may be traced by the measurement of the ratio of stable nitrogen isotopes (δ(15)N). In this study δ(15)N was determined in two species of macroalgae (Ascophyllum nodosum and Fucus vesiculosus), and in nitrate and ammonium to determine the relative importance of anthropogenic versus natural sources of nitrogen along the coast of NW Spain. Both algal species and nitrogen sources showed similar isotopic enrichment for a given site, but algal δ(15)N was not related to either inorganic nitrogen concentrations or δ(15)N in the water samples. The latter suggests that inorganic nitrogen inputs are variable and do not always leave an isotopic trace in macroalgae. However, a significant linear decrease in macroalgal δ(15)N along the coast is consistent with the differential effect of upwelling. Besides this geographic variability, the influence of anthropogenic nitrogen sources is evidenced by higher δ(15)N in macroalgae from rias and estuaries compared to those from open coastal areas and in areas with more than 15×10(3) inhabitants in the watershed. These results indicate that, in contrast with other studies, macroalgal δ(15)N is not simply related to either inorganic nitrogen concentrations or human population size but depends on other factors as the upwelling or the efficiency of local waste treatment systems. Copyright © 2012 Elsevier B.V. All rights reserved.
NASA Astrophysics Data System (ADS)
Roberts, C.
2008-12-01
The Holocene has witnessed a switch from a nature-dominated to a human-dominated Earth system. Although globally-significant human impacts (wildfire, megafaunal extinctions) occurred during the late Pleistocene, it was the advent of agriculture that led to the progressive transformation of land cover, and which distinguishes the Holocene from previous interglacial periods. A wide array of data provide clear evidence of local-to-regional human disturbance from ~5 ka BP, in some cases earlier. There is more uncertainty about when the anthropogenic "footprint" became detectable at a global scale, and there has consequently been debate about how much of the pre-industrial increase in atmospheric greenhouse gas concentrations is attributable to human causation, linked to processes such as deforestation (CO2) and wet rice cultivation (CH4). Although there has been recent progress in developing quantitative methods for translating pollen data into palaeo-land cover, such as the REVEALS model of Sugita (Holocene 2007) coupled to GIS, this has yet to be widely applied to existing data bases, and most pollen-based land-use reconstructions remain qualitative or semi-quantitative. Lake trophic status, sediment flux / soil erosion, and microcharcoal records of biomass burning provide alternative proxies that integrate regional-scale landscape disturbance. These proxy data along with documentary sources imply that globally-significant changes in land cover occurred prior to ~250 BP which must have altered atmospheric greenhouse gas concentrations by this time. The polarised debate for and against early anthropogenic impact on global carbon cycling mirrors our industrial-era division between nature and society, both conceptually (e.g. Cartesian dualism) and on the ground (e.g. demarcating land between monoculture agriculture and wilderness). However, for the period before ~1750 AD, this likely represents a false dichotomy, because pre-industrial societies more often formed part of the natural world, while at the same time modifying and transforming it. Attempts to partition carbon emissions between natural and anthropogenic sources during the Holocene may therefore be misplaced. Many landscapes, such as savannas, are the result of synergistic - and in some cases contingent - relationships between people, other animals, plants and other components of nature. The issue is thus not whether early humans altered carbon cycling (they did), but rather at what point it became detectable at a global scale, and what form it took.
Lead isotopes and trace metal ratios of aerosols as tracers of Pb pollution sources in Kanpur, India
NASA Astrophysics Data System (ADS)
Sen, Indra; Bizimis, Michael; Tripathi, Sachchida; Paul, Debajyoti; Tyagi, Swati; Sengupta, Deep
2015-04-01
The anthropogenic flux of Pb in the Earth's surface is almost an order of magnitude higher than its corresponding natural flux [1]. Identifying the sources and pathways of anthropogenic Pb in environment is important because Pb toxicity is known to have adverse effects on human health. Pb pollution sources for America, Europe, and China are well documented. However, sources of atmospheric Pb are unknown in India, particularly after leaded gasoline was phased out in 2000. India has a developing economy with a rapidly emerging automobile and high temperature industry, and anthropogenic Pb emission is expected to rise in the next decade. In this study, we report on the Pb- isotope compositions and trace metal ratios of airborne particulates collected in Kanpur, an industrial city in northern India. The Pb concentration in the airborne particulate matter varies between 14-216 ng/m3, while the other heavy metals vary by factor of 10 or less, e.g. Cd=0.3-3 ng/m3, As=0.4-3.5 ng/m3, Zn=36-161 ng/m3, and Cu=3-22 ng/m3. The 206Pb/207Pb, 208Pb/206Pb, and 208Pb/207Pb vary between 1.112 - 1.129, 2.123-2.141, and 2.409-2.424 respectively, and are highly correlated with each other (R2>0.9). Pb isotopes and trace metal data reveals that coal combustion is the major source of anthropogenic Pb in the atmosphere, with limited contribution from mining and smelting processes. We further conclude that combination of Pb isotope ratios and V/Pb ratios are powerful tracers for Pb source apportionment studies, which is otherwise difficult to differentiate based only on Pb systematics [1] Sen and Peucker-Ehrenbrink (2012), Environ. Sci. Technol.(46), 8601-8609
NASA Astrophysics Data System (ADS)
Garland, R. M.; Naidoo, M.; Dedekind, Z.; Sibiya, B.; Piketh, S.; Engelbrecht, C. J.; Engelbrecht, F.
2017-12-01
Many parts of the southern hemisphere are linked in part due to the strong impact that emissions from natural sources, such as large biomass burning events and marine sources, as well as growing anthropogenic emission sources. Most of southern Africa has an arid to semi-arid climate that is strongly impacted by biomass burning, biogenic and dust emissions. In addition, there are areas of growing industrialization and urbanization that contributes to poor air quality. This air pollution can impact not only human health, but also agriculture, ecosystems, and the climate. This presentation will highlight on-going research to simulate the southern Africa atmosphere and impacts, with a focus on the interplay and relative importance of natural and anthropogenic emissions. The presentation will discuss the simulated sensitivity of the southern African climate to aerosol particles to highlight the importance of natural sources. These historical simulations (1979-2012) were performed with CCAM and are towards the development of the first Africa-led earth systems model. The analysis focused on the simulated sensitivity of the climate and clouds off the southwestern coast of Africa to aerosol particles. The interplay between natural and anthropogenic sources on air pollution will be highlighted using the Waterberg region of South Africa as a case study. CAMx was run at 2km resolution for 2013 using local emission inventories and meteorological output from CCAM to simulate the air quality of the region. These simulations estimate that, on average in the summer, up to 20% of ozone in and around a power plant plume is attributable to biogenic sources of VOCs, with ozone peaks of up to 120ppb; highlighting the importance of understanding the mix of pollutants in this area. In addition to presenting results from this study, the challenges in modelling will be highlighted. These challenges include very few or no measurements that are important to understand, and then accurately simulate, atmospheric chemistry (e.g. OH, PAN, SOA).
Primary and secondary organic aerosols in summer 2016 in Beijing
NASA Astrophysics Data System (ADS)
Tang, Rongzhi; Wu, Zepeng; Li, Xiao; Wang, Yujue; Shang, Dongjie; Xiao, Yao; Li, Mengren; Zeng, Limin; Wu, Zhijun; Hallquist, Mattias; Hu, Min; Guo, Song
2018-03-01
To improve air quality, the Beijing government has employed several air pollution control measures since the 2008 Olympics. In order to investigate organic aerosol sources after the implementation of these measures, ambient fine particulate matter was collected at a regional site in Changping (CP) and an urban site at the Peking University Atmosphere Environment Monitoring Station (PKUERS) during the Photochemical Smog in China
field campaign in summer 2016. Chemical mass balance (CMB) modeling and the tracer yield method were used to apportion primary and secondary organic sources. Our results showed that the particle concentration decreased significantly during the last few years. The apportioned primary and secondary sources explained 62.8 ± 18.3 and 80.9 ± 27.2 % of the measured OC at CP and PKUERS, respectively. Vehicular emissions served as the dominant source. Except for gasoline engine emissions, the contributions of all the other primary sources decreased. In addition, the anthropogenic SOC, i.e., toluene SOC, also decreased, implying that deducting primary emissions can reduce anthropogenic SOA. In contrast to the SOA from other regions in the world where biogenic SOA was dominant, anthropogenic SOA was the major contributor to SOA, implying that deducting anthropogenic VOC emissions is an efficient way to reduce SOA in Beijing. Back-trajectory cluster analysis results showed that high mass concentrations of OC were observed when the air mass was from the south. However, the contributions of different primary organic sources were similar, suggesting regional particle pollution. The ozone concentration and temperature correlated well with the SOA concentration. Different correlations between day and night samples suggested different SOA formation pathways. Significant enhancement of SOA with increasing particle water content and acidity was observed in our study, suggesting that aqueous-phase acid-catalyzed reactions may be the important SOA formation mechanism in summer in Beijing.
A summary and comparison of bird mortality from anthropogenic causes with an emphasis on collisions
Wallace P. Erickson; Gregory D. Johnson; David P. Jr. Young
2005-01-01
We estimate that from 500 million to possibly over 1 billion birds are killed annually in the United States due to anthropogenic sources including collisions with human-made structures such as vehicles, buildings and windows, power lines, communication towers, and wind turbines; electrocutions; oil spills and other contaminants; pesticides; cat predation; and...
NASA Astrophysics Data System (ADS)
Pirrone, N.; Costa, P.; Pacyna, J. M.; Ferrara, R.
This report discusses past, current and projected mercury emissions to the atmosphere from major industrial sources, and presents a first assessment of the contribution to the regional mercury budget from selected natural sources. Emissions (1995 estimates) from fossil fuels combustion (29.8 t yr -1) , cement production (28.8 t yr -1) and incineration of solid wastes (27.6 t yr -1) , all together account for about 82% of the regional anthropogenic total (105.7 t yr -1) . Other industrial sources in the region are smelters (4.8 t yr -1) , iron-steel plants (4.8 t yr -1) and other minor sources (chlor-alkali plants, crematoria, chemicals production) that have been considered together in the miscellaneous category (9.6 t yr -1) . Regional emissions from anthropogenic sources increased at a rate of 3% yr-1 from 1983 to 1995 and are projected to increase at a rate of 1.9% yr-1 in the next 25 years, if no improvement in emission control policy occurs. On a country-by-country basis, France is the leading emitter country with 22.6 t yr -1 followed by Turkey (16.1 t yr -1) , Italy (11.4 t yr -1) , Spain (9.1 t yr -1) , the former Yugoslavia 7.9 ( t yr -1) , Morocco (6.9 t yr -1) , Bulgaria (6.8 t yr -1) , Egypt (6.1 t yr -1) , Syria (3.6 t yr -1) , Libya (2.9 t yr -1) , Tunisia (2.8 t yr -1) and Greece (2.7 t yr -1) , whereas the remaining countries account for less than 7% of the regional total. The annual emission from natural sources is 110 t yr -1, although this figure only includes the volatilisation of elemental mercury from surface waters and emissions from volcanoes, whereas the contribution due to the degassing of mercury from top soil and vegetation has not been included in this first assessment. Therefore, natural and anthropogenic sources in the Mediterranean region release annually about 215 t of mercury, which represents a significant contribution to the total mercury budget released in Europe and to the global atmosphere.
Dong, Zhicheng; Bao, Zhengyu; Wu, Guoai; Fu, Yangrong; Yang, Yi
2010-11-01
The content and spatial distribution of lead in the aquatic systems in two Chinese tropical cities in Hainan province (Haikou and Sanyan) show an unequal distribution of lead between the urban and the suburban areas. The lead content is significantly higher (72.3 mg/kg) in the urban area than the suburbs (15.0 mg/kg) in Haikou, but quite equal in Sanya (41.6 and 43.9 mg/kg). The frequency distribution histograms suggest that the lead in Haikou and in Sanya derives from different natural and/or anthropogenic sources. The isotopic compositions indicate that urban sediment lead in Haikou originates mainly from anthropogenic sources (automobile exhaust, atmospheric deposition, etc.) which contribute much more than the natural sources, while natural lead (basalt and sea sands) is still dominant in the suburban areas in Haikou. In Sanya, the primary source is natural (soils and sea sands).
Wildfire air pollution hazard during the 21st century
NASA Astrophysics Data System (ADS)
Knorr, Wolfgang; Dentener, Frank; Lamarque, Jean-François; Jiang, Leiwen; Arneth, Almut
2017-07-01
Wildfires pose a significant risk to human livelihoods and are a substantial health hazard due to emissions of toxic smoke. Previous studies have shown that climate change, increasing atmospheric CO2, and human demographic dynamics can lead to substantially altered wildfire risk in the future, with fire activity increasing in some regions and decreasing in others. The present study re-examines these results from the perspective of air pollution risk, focussing on emissions of airborne particulate matter (PM2. 5), combining an existing ensemble of simulations using a coupled fire-dynamic vegetation model with current observation-based estimates of wildfire emissions and simulations with a chemical transport model. Currently, wildfire PM2. 5 emissions exceed those from anthropogenic sources in large parts of the world. We further analyse two extreme sets of future wildfire emissions in a socio-economic, demographic climate change context and compare them to anthropogenic emission scenarios reflecting current and ambitious air pollution legislation. In most regions of the world, ambitious reductions of anthropogenic air pollutant emissions have the potential to limit mean annual pollutant PM2. 5 levels to comply with World Health Organization (WHO) air quality guidelines for PM2. 5. Worst-case future wildfire emissions are not likely to interfere with these annual goals, largely due to fire seasonality, as well as a tendency of wildfire sources to be situated in areas of intermediate population density, as opposed to anthropogenic sources that tend to be highest at the highest population densities. However, during the high-fire season, we find many regions where future PM2. 5 pollution levels can reach dangerous levels even for a scenario of aggressive reduction of anthropogenic emissions.
NASA Astrophysics Data System (ADS)
Costigan, K. R.; Dubey, M. K.; Chylek, P.; Love, S. P.; Henderson, B. G.; Flowers, B. A.; Reisner, J. M.; Rahn, T.; Quick, C. R.
2010-12-01
Agreements to limit greenhouse gas emissions require scientifically valid methods for monitoring and validating anthropogenic emissions. However, the task of monitoring CO2 emissions is difficult because relatively small increases need to be detected against CO2’s variable and large background concentrations. To ensure fair compliance, remotely sensed measurements and an understanding of the atmospheric transport of CO2 from the sources are required. We hypothesize that CO2 from various natural and anthropogenic sources can be distinguished and tracked by monitoring co-emitted gases (e.g. NO2, SO2, and CO) and isotopomers (e.g.13CO2). The ratio of a co-emitted species to CO2 depends on fuel composition and combustion process and thus varies by energy sector. These ratios provide an independent method to quantify CO2 emissions. Their low backgrounds, their large perturbations from energy activities, and our ability to measure them precisely make them sensitive probes to attribute sources, especially when emission ratios of multiple species are used concurrently. This strategy of observing emission ratios of co-emitted species to derive regional and source-specific baselines and CO2 fluxes is being tested in the Four Corners region of northwestern New Mexico. The semi-arid ecology in the region has a weak natural carbon cycle, facilitating our goal of dissection of anthropogenic sector-specific sources. The net Four Corners and San Juan power plant emissions are the largest point source of CO2 and NOx in North America. The Four Corners plant produces much more NOx than the San Juan power plant, while their energy and CO2 outputs, and coal used, are similar. This difference offers us a unique opportunity to test discrimination methods. While their CO2 signals remain elusive for current satellites, their NO2 plumes have recently been resolved from space. The region also experiences dispersed CO2 urban emissions as well as emissions and leaks from thousands of oil/gas wells. All of this makes the site an ideal test-bed. Our approach is to execute a systematic and coordinated observational, satellite validation and modeling program. We are instrumenting the Four Corners ground site with an array of state-of-the art, in situ and remote sensors, including LANL’s solar FTS and in situ sensors for continuous long term monitoring. Satellite measurements are also analyzed and have revealed that recent environmental upgrades have reduced NOx emissions, verifying bottom up inventories. A coordinated field campaign is planned, which will interrogate the power plant plume and regional dynamics and chemistry. Modeling using the plants’ reported emissions will be compared with observations to test the veracity of our approach. Early modeling, satellite analyses and measurements will be presented.
Nitrogen oxides (NOX) are important components of ambient and indoor air pollution and are emitted from a range of combustion sources, including on-road mobile sources, electric power generators, and non-road mobile sources. While anthropogenic sources dominate, NOX is also forme...
Keil, Richard; Salemme, Keri; Forrest, Brittany; Neibauer, Jaqui; Logsdon, Miles
2011-11-01
Organic compounds were evaluated in March 2010 at 22 stations in Barkley Sound, Vancouver Island Canada and at 66 locations in Puget Sound. Of 37 compounds, 15 were xenobiotics, 8 were determined to have an anthropogenic imprint over natural sources, and 13 were presumed to be of natural or mixed origin. The three most frequently detected compounds were salicyclic acid, vanillin and thymol. The three most abundant compounds were diethylhexyl phthalate (DEHP), ethyl vanillin and benzaldehyde (∼600 n g L(-1) on average). Concentrations of xenobiotics were 10-100 times higher in Puget Sound relative to Barkley Sound. Three compound couplets are used to illustrate the influence of human activity on marine waters; vanillin and ethyl vanillin, salicylic acid and acetylsalicylic acid, and cinnamaldehyde and cinnamic acid. Ratios indicate that anthropogenic activities are the predominant source of these chemicals in Puget Sound. Published by Elsevier Ltd.
NASA Astrophysics Data System (ADS)
Guittard, A.; Baraer, M.; McKenzie, J. M.; Mark, B. G.; Fernandez, A.; Walsh, E.; Santos Perez, A.
2015-12-01
The Rio Santa, Peru, drains the western slopes of the glacierized Cordillera Blanca and provides water resources at almost all levels of the watershed. As it flows away from the valleys of the Cordillera Blanca, the Rio Santa takes out pollution from numerous sources, including acid mine drainage and natural sulfide oxidation by-products. The Rio Santa dry season discharge decline that is projected to be a consequence of glaciers retreat will probably have implications for the evolution of water pollution. This threat makes the characterization of the actual contamination mechanisms of primary importance. The present study focuses, first, on the spatiotemporal variability of heavy metal contamination across the entire Rio Santa Watershed and secondly on differentiating anthropogenic and natural contaminated sites. First, a macroscale sampling has been done during the summer 2013 to provide an overview of the contamination by trace metal, in water, suspended sediments and riverbed sediments. In addition, 30 water samples were taken from a point next to the city of Huaraz at a frequency of once every 2 weeks and analyzed for trace metals. Secondly, in order to identify hydrochemical contaminant origin dependant signatures in the Rio Santa watershed, 5 areas of known contamination origins were sampled during the summer 2014.Spatially speaking, we observed that most pollution is located in the south of the watershed, and that a large part of the arsenic that reaches the Santa in an aqueous phase does not make it to the outlet but remains trapped in the riverbed. Annual variation in water shows a very unusual fluctuation in Mn compare to other trace metal which are relatively stable. By differencing anthropogenic and natural sites and by considering glaciers melt and decrease water in future what would be the impact of the part of natural contaminated sites versus anthropogenic, mining and cities, on the water quality? Preliminary results show that anthropogenic sites show high level of As and Cd but natural contaminated sites show high level of Al, Fe and Mn.
PROVIDING SAFE WATER TO RURAL NEPAL: A NOVEL WATER FILTRATION SYSTEM
The quality of Nepalese water sources is often compromised by pathogen contamination resulting from inadequate wastewater management, and arsenic contamination from natural and anthropogenic sources. The primary source of Nepal’s arsenic problem is suspected to arise fro...
NASA Astrophysics Data System (ADS)
Myint, S. W.; Zheng, B.; Fan, C.; Kaplan, S.; Brazel, A.; Middel, A.; Smith, M.
2014-12-01
While the relationship between fractional cover of anthropogenic and vegetation features and the urban heat island has been well studied, the effect of spatial arrangements (e.g., clustered, dispersed) of these features on urban warming or cooling are not well understood. The goal of this study is to examine if and how spatial configuration of land cover features influence land surface temperatures (LST) in urban areas. This study focuses on Phoenix, AZ and Las Vegas, NV that have undergone dramatic urban expansion. The data used to classify detailed urban land cover types include Geoeye-1 (Las Vegas) and QuickBird (Phoenix). The Geoeye-1 image (3 m resolution) was acquired on October 12, 2011 and the QuickBird image (2.4 m resolution) was taken on May 29, 2007. Classification was performed using object based image analysis (OBIA). We employed a spatial autocorrelation approach (i.e., Moran's I) that measures the spatial dependence of a point to its neighboring points and describes how clustered or dispersed points are arranged in space. We used Advanced Spaceborne Thermal Emission and Reflection Radiometer (ASTER) data acquired over Phoenix (daytime on June 10, 2011 and nighttime on October 17, 2011) and Las Vegas (daytime on July 6, 2005 and nighttime on August 27, 2005) to examine daytime and nighttime LST with regards to the spatial arrangement of anthropogenic and vegetation features. We spatially correlate Moran's I values of each land cover per surface temperature, and develop regression models. The spatial configuration of grass and trees shows strong negative correlations with LST, implying that clustered vegetation lowers surface temperatures more effectively. In contrast, a clustered spatial arrangement of anthropogenic land-cover features, especially impervious surfaces, significantly elevates surface temperatures. Results from this study suggest that the spatial configuration of anthropogenic and vegetation features influence urban warming and cooling.
Modelling prehistoric terrain Models using LiDAR-data: a geomorphological approach
NASA Astrophysics Data System (ADS)
Höfler, Veit; Wessollek, Christine; Karrasch, Pierre
2015-10-01
Terrain surfaces conserve human activities in terms of textures and structures. With reference to archaeological questions, the geological archive is investigated by means of models regarding anthropogenic traces. In doing so, the high-resolution digital terrain model is of inestimable value for the decoding of the archive. The evaluation of these terrain models and the reconstruction of historical surfaces is still a challenging issue. Due to the data collection by means of LiDAR systems (light detection and ranging) and despite their subsequent pre-processing and filtering, recently anthropogenic artefacts are still present in the digital terrain model. Analysis have shown that elements, such as contour lines and channels, can well be extracted from a high-resolution digital terrain model. This way, channels in settlement areas show a clear anthropogenic character. This fact can also be observed for contour lines. Some contour lines representing a possibly natural ground surface and avoid anthropogenic artefacts. Comparable to channels, noticeable patterns of contour lines become visible in areas with anthropogenic artefacts. The presented workflow uses functionalities of ArcGIS and the programming language R.1 The method starts with the extraction of contour lines from the digital terrain model. Through macroscopic analyses based on geomorphological expert knowledge, contour lines are selected representing the natural geomorphological character of the surface. In a first step, points are determined along each contour line in regular intervals. This points and the corresponding height information which is taken from an original digital terrain model is saved as a point cloud. Using the programme library gstat, a variographic analysis and the use of a Kriging-procedure based on this follow.2-4 The result is a digital terrain model filtered considering geomorphological expert knowledge showing no human degradation in terms of artefacts, preserving the landscape-genetic character and can be called a prehistoric terrain model.
Nitrous Oxide: A Greenhouse Gas That is Also an Ozone Layer Depleting Gas
NASA Astrophysics Data System (ADS)
Reed, S.; Uriarte, M.; Wood, T. E.; Cavaleri, M. A.; Lugo, A. E.
2014-12-01
Nitrous oxide, N2O, is the major source of nitrogen oxides in the stratosphere, where these oxides playa critical roles in ozone layer depletion by itself and moderating ozone layer depletion by chlorinated chemicals. Thus N2O plays a complex role in the stratosphere. Nitrous oxide is also a greenhouse gas and it contributes to the radiative forcing of climate. Indeed, it is considered the third most important greenhouse gas next to carbon dioxide and methane. This dual role of nitrous oxide makes it an interesting gas for the atmosphere- it bridges the issue of ozone layer depletion and climate change. Nitrous oxide has both natural and anthropogenic sources. Therefore, one needs to consider this important distinction between natural and anthropogenic sources as well as its role in two related but separate environmental issues. Further, the sources of nitrous oxide are varied and diffuse, which makes it difficult to quantify different sources. However, it is clear that a majority of anthropogenic nitrous oxide comes from food production (including agricultural and animal growth practices), an activity that is at the heart of human existence. Thus, limiting N2O emissions is not a simple task! I will briefly summarize our understanding of these roles of nitrous oxide in the earth's atmosphere and touch on the possible ways to limit N2O emissions.
Nitrous Oxide: A Greenhouse Gas That is Also an Ozone Layer Depleting Gas
NASA Astrophysics Data System (ADS)
Ravishankara, A. R.
2015-12-01
Nitrous oxide, N2O, is the major source of nitrogen oxides in the stratosphere, where these oxides playa critical roles in ozone layer depletion by itself and moderating ozone layer depletion by chlorinated chemicals. Thus N2O plays a complex role in the stratosphere. Nitrous oxide is also a greenhouse gas and it contributes to the radiative forcing of climate. Indeed, it is considered the third most important greenhouse gas next to carbon dioxide and methane. This dual role of nitrous oxide makes it an interesting gas for the atmosphere- it bridges the issue of ozone layer depletion and climate change. Nitrous oxide has both natural and anthropogenic sources. Therefore, one needs to consider this important distinction between natural and anthropogenic sources as well as its role in two related but separate environmental issues. Further, the sources of nitrous oxide are varied and diffuse, which makes it difficult to quantify different sources. However, it is clear that a majority of anthropogenic nitrous oxide comes from food production (including agricultural and animal growth practices), an activity that is at the heart of human existence. Thus, limiting N2O emissions is not a simple task! I will briefly summarize our understanding of these roles of nitrous oxide in the earth's atmosphere and touch on the possible ways to limit N2O emissions.
NASA Astrophysics Data System (ADS)
Kara, Melik; Dumanoglu, Yetkin; Altiok, Hasan; Elbir, Tolga; Odabasi, Mustafa; Bayram, Abdurrahman
2014-11-01
Atmospheric bulk deposition (wet + dry deposition) samples (n = 40) were collected concurrently at ten sites in four seasons between June 2009 and April 2010 in the Aliaga heavily industrialized region, Turkey, containing a number of significant air pollutant sources. Analyses of trace elements were carried out using inductively coupled plasma-mass spectrometry (ICP-MS). While there were significant differences in the particulate matter (PM) deposition fluxes among the sampling sites, seasonal variations were not statistically significant (Kruskal-Wallis test, p < 0.05). Both PM deposition and elemental fluxes were increased at the sampling sites in the vicinity of industrial activities. The crustal elements (i.e., Ca, Mg) and some anthropogenic elements (such as Fe, Zn, Mn, Pb, Cu, and Cr) were high, and the highest fluxes were mostly measured in summer and winter seasons. The enrichment factor (EF) and principal component analysis (PCA) was applied to the data to determine the possible sources in the study area. High EF values were obtained for the anthropogenic elements such as Ag, Cd, Zn, Pb, Cu and Sb. The possible sources were identified as anthropogenic sources (i.e., iron-steel production) (45.4%), crustal and re-suspended dust (27.1%), marine aerosol (7.9%), and coal and wood combustion (8.2%). Thus, the iron-steel production and its related activities were found to be the main pollutant sources for this region.
Use of Tritium Accelerator Mass Spectrometry for Tree Ring Analysis
LOVE, ADAM H.; HUNT, JAMES R.; ROBERTS, MARK L.; SOUTHON, JOHN R.; CHIARAPPA - ZUCCA, MARINA L.; DINGLEY, KAREN H.
2010-01-01
Public concerns over the health effects associated with low-level and long-term exposure to tritium released from industrial point sources have generated the demand for better methods to evaluate historical tritium exposure levels for these communities. The cellulose of trees accurately reflects the tritium concentration in the source water and may contain the only historical record of tritium exposure. The tritium activity in the annual rings of a tree was measured using accelerator mass spectrometry to reconstruct historical annual averages of tritium exposure. Milligram-sized samples of the annual tree rings from a Tamarix located at the Nevada Test Site are used for validation of this methodology. The salt cedar was chosen since it had a single source of tritiated water that was well-characterized as it varied over time. The decay-corrected tritium activity of the water in which the salt cedar grew closely agrees with the organically bound tritium activity in its annual rings. This demonstrates that the milligram-sized samples used in tritium accelerator mass spectrometry are suited for reconstructing anthropogenic tritium levels in the environment. PMID:12144257
NASA Astrophysics Data System (ADS)
Christianson, E. M.; Keeler, G. J.; Landis, M. S.
2008-12-01
Mercury (Hg) is a bioaccumulative neurotoxin that has been shown to enter water bodies, and consequently the food chain, via atmospheric deposition to the earth's surface. Anthropogenic emissions of the pollutant play a significant role in contributing to the atmospheric pool of Hg, but the near filed impact from point source on surface deposition has been poorly defined to date. An intensive study during July-September 2006 established eight networked precipitation collection sites in northeastern Ohio, U.S.A., located at varying proximities to coal combustion facilities to evaluate the spatial scale of Hg wet deposition concentration enhancement about the sources. It was found that an average of 42% of the Hg wet deposited at sites in the immediate vicinity (<1 km) of coal fired utilities could be attributed to that adjacent source. Several meteorological variables were shown to account for the degree to which Hg concentration in precipitation was enhanced. A detailed meteorological analysis of the individual precipitation events as well as overall implications of local deposition gradients will be discussed.
Morgan, Michael B; Edge, Sara E; Snell, Terry W
2005-01-01
A coral cDNA array containing 32 genes was used to examine the gene expression profiles of coral populations located at four sites that varied with distance from a semi-submerged municipal dump in Castle Harbour, Bermuda (previously identified as a point source of anthropogenic stressors). Genes on the array represent transcripts induced under controlled laboratory conditions to a variety of stressors both natural (temperature, sediment, salinity, darkness) and xenobiotic (heavy metals, pesticides, PAH) in origin. The gene expression profiles produced revealed information about the types of stressors. Consistent with other studies undertaken in Castle Harbour, the coral cDNA array detected responses to heavy metals, sedimentation, as well as oxidative stress.
Tropospheric ozone using an emission tagging technique in the CAM-Chem and WRF-Chem models
NASA Astrophysics Data System (ADS)
Lupascu, A.; Coates, J.; Zhu, S.; Butler, T. M.
2017-12-01
Tropospheric ozone is a short-lived climate forcing pollutant. High concentration of ozone can affect human health (cardiorespiratory and increased mortality due to long-term exposure), and also it damages crops. Attributing ozone concentrations to the contributions from different sources would indicate the effects of locally emitted or transported precursors on ozone levels in specific regions. This information could be used as an important component of the design of emissions reduction strategies by indicating which emission sources could be targeted for effective reductions, thus reducing the burden of ozone pollution. Using a "tagging" approach within the CAM-Chem (global) and WRF-Chem (regional) models, we can quantify the contribution of individual emission of NOx and VOC precursors on air quality. Hence, when precursor emissions of NOx are tagged, we have seen that the largest contributors on ozone levels are the anthropogenic sources, while in the case of precursor emissions of VOCs, the biogenic sources and methane account for more than 50% of ozone levels. Further, we have extended the NOx tagging method in order to investigate continental source region contributions to concentrations of ozone over various receptor regions over the globe, with a zoom over Europe. In general, summertime maximum ozone in most receptor regions is largely attributable to local emissions of anthropogenic NOx and biogenic VOC. During the rest of the year, especially during springtime, ozone in most receptor regions shows stronger influences from anthropogenic emissions of NOx and VOC in remote source regions.
Nitrate pollution and surface water chemistry in Shimabara, Nagasaki Prefecture, Japan
NASA Astrophysics Data System (ADS)
Nakagawa, K.; Amano, H.
2017-12-01
Shimabara city has been experiencing serious nitrate pollution in groundwater. To evaluate nitrate pollution and water chemistry in surface water, water samples were collected at 42 sampling points in 15 rivers in Shimabara including a part of Unzen city from January to February 2017. Firstly, spatial distribution of water chemistry was assessed by describing stiff and piper-trilinear diagrams using major ions concentrations. Most of the samples showed Ca-HCO3 or Ca-(NO3+SO4) water types. It corresponds to groundwater chemistry. Some samples were classified into characteristic water types such as Na-Cl, (Na+K)-HCO3, and Ca-Cl. These results indicate sea water mixing and anthropogenic pollution. At the upstream of Nishi-river, although water chemistry showed Ca-HCO3, ions concentrations were higher than that of the other rivers. It indicates that this site was affected by the peripheral anthropogenic activities. Secondly, nitrate-pollution assessment was performed by using NO3-, NO2-, coprostanol (5β(H)-Cholestan-3β-ol), and cholestanol (5α(H)-Cholestan-3β-ol). NO2-N was detected at the 2 sampling points and exceeded drinking standard 0.9 mg L-1 for bottle-fed infants (WHO, 2011). NO3-N + NO2-N concentrations exceeded Japanese drinking standard 10 mg L-1 at 18 sampling points. The highest concentration was 27.5 mg L-1. Higher NO3-N levels were observed in the rivers in the northern parts of the study area. Coprostanol has been used as a fecal contamination indicator, since it can be found in only feces of higher animals. Coprostanol concentrations at 8 sampling points exceeded 700 ng L-1 (Australian drinking water standard). Coprostanol has a potential to distinguish the nitrate pollution sources between chemical fertilizer or livestock wastes, since water samples with similar NO3-N + NO2-N concentration showed distinct coprostanol concentration. The sterols ratio (5β/ (5β+5α)) exceeded 0.5 at 18 sampling points. This reveals that fecal pollution has occurred.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Maasakkers, Joannes D.; Jacob, Daniel J.; Sulprizio, Melissa P.
Here we present a gridded inventory of US anthropogenic methane emissions with 0.1° × 0.1° spatial resolution, monthly temporal resolution, and detailed scaledependent error characterization. The inventory is designed to be consistent with the 2016 US Environmental Protection Agency (EPA) Inventory of US Greenhouse Gas Emissions and Sinks (GHGI) for 2012. The EPA inventory is available only as national totals for different source types. We use a wide range of databases at the state, county, local, and point source level to disaggregate the inventory and allocate the spatial and temporal distribution of emissions for individual source types. Results show largemore » differences with the EDGAR v4.2 global gridded inventory commonly used as a priori estimate in inversions of atmospheric methane observations. We derive grid-dependent error statistics for individual source types from comparison with the Environmental Defense Fund (EDF) regional inventory for Northeast Texas. These error statistics are independently verified by comparison with the California Greenhouse Gas Emissions Measurement (CALGEM) grid-resolved emission inventory. Finally, our gridded, time-resolved inventory provides an improved basis for inversion of atmospheric methane observations to estimate US methane emissions and interpret the results in terms of the underlying processes.« less
Gridded National Inventory of U.S. Methane Emissions
NASA Technical Reports Server (NTRS)
Maasakkers, Joannes D.; Jacob, Daniel J.; Sulprizio, Melissa P.; Turner, Alexander J.; Weitz, Melissa; Wirth, Tom; Hight, Cate; DeFigueiredo, Mark; Desai, Mausami; Schmeltz, Rachel;
2016-01-01
We present a gridded inventory of US anthropogenic methane emissions with 0.1 deg x 0.1 deg spatial resolution, monthly temporal resolution, and detailed scale dependent error characterization. The inventory is designed to be onsistent with the 2016 US Environmental Protection Agency (EPA) Inventory of US Greenhouse Gas Emissionsand Sinks (GHGI) for 2012. The EPA inventory is available only as national totals for different source types. We use a widerange of databases at the state, county, local, and point source level to disaggregate the inventory and allocate the spatial and temporal distribution of emissions for individual source types. Results show large differences with the EDGAR v4.2 global gridded inventory commonly used as a priori estimate in inversions of atmospheric methane observations. We derive grid-dependent error statistics for individual source types from comparison with the Environmental Defense Fund (EDF) regional inventory for Northeast Texas. These error statistics are independently verified by comparison with the California Greenhouse Gas Emissions Measurement (CALGEM) grid-resolved emission inventory. Our gridded, time-resolved inventory provides an improved basis for inversion of atmospheric methane observations to estimate US methane emissions and interpret the results in terms of the underlying processes.
Gridded national inventory of U.S. methane emissions
Maasakkers, Joannes D.; Jacob, Daniel J.; Sulprizio, Melissa P.; ...
2016-11-16
Here we present a gridded inventory of US anthropogenic methane emissions with 0.1° × 0.1° spatial resolution, monthly temporal resolution, and detailed scaledependent error characterization. The inventory is designed to be consistent with the 2016 US Environmental Protection Agency (EPA) Inventory of US Greenhouse Gas Emissions and Sinks (GHGI) for 2012. The EPA inventory is available only as national totals for different source types. We use a wide range of databases at the state, county, local, and point source level to disaggregate the inventory and allocate the spatial and temporal distribution of emissions for individual source types. Results show largemore » differences with the EDGAR v4.2 global gridded inventory commonly used as a priori estimate in inversions of atmospheric methane observations. We derive grid-dependent error statistics for individual source types from comparison with the Environmental Defense Fund (EDF) regional inventory for Northeast Texas. These error statistics are independently verified by comparison with the California Greenhouse Gas Emissions Measurement (CALGEM) grid-resolved emission inventory. Finally, our gridded, time-resolved inventory provides an improved basis for inversion of atmospheric methane observations to estimate US methane emissions and interpret the results in terms of the underlying processes.« less
Gridded National Inventory of U.S. Methane Emissions.
Maasakkers, Joannes D; Jacob, Daniel J; Sulprizio, Melissa P; Turner, Alexander J; Weitz, Melissa; Wirth, Tom; Hight, Cate; DeFigueiredo, Mark; Desai, Mausami; Schmeltz, Rachel; Hockstad, Leif; Bloom, Anthony A; Bowman, Kevin W; Jeong, Seongeun; Fischer, Marc L
2016-12-06
We present a gridded inventory of US anthropogenic methane emissions with 0.1° × 0.1° spatial resolution, monthly temporal resolution, and detailed scale-dependent error characterization. The inventory is designed to be consistent with the 2016 US Environmental Protection Agency (EPA) Inventory of US Greenhouse Gas Emissions and Sinks (GHGI) for 2012. The EPA inventory is available only as national totals for different source types. We use a wide range of databases at the state, county, local, and point source level to disaggregate the inventory and allocate the spatial and temporal distribution of emissions for individual source types. Results show large differences with the EDGAR v4.2 global gridded inventory commonly used as a priori estimate in inversions of atmospheric methane observations. We derive grid-dependent error statistics for individual source types from comparison with the Environmental Defense Fund (EDF) regional inventory for Northeast Texas. These error statistics are independently verified by comparison with the California Greenhouse Gas Emissions Measurement (CALGEM) grid-resolved emission inventory. Our gridded, time-resolved inventory provides an improved basis for inversion of atmospheric methane observations to estimate US methane emissions and interpret the results in terms of the underlying processes.
Decline in Chinese lake phosphorus concentration accompanied by shift in sources since 2006
NASA Astrophysics Data System (ADS)
Tong, Yindong; Zhang, Wei; Wang, Xuejun; Couture, Raoul-Marie; Larssen, Thorjørn; Zhao, Yue; Li, Jing; Liang, Huijiao; Liu, Xueyan; Bu, Xiaoge; He, Wei; Zhang, Qianggong; Lin, Yan
2017-07-01
Domestic wastewater and agricultural activities are important sources of nutrient pollutants such as phosphorus and nitrogen. Upon reaching freshwater, these nutrients can lead to extensive growth of harmful algae, which results in eutrophication. Many Chinese lakes are subject to such eutrophication, especially in highly polluted areas, and as such, understanding nutrient fluxes to these lakes offers insights into the varying processes governing pollutant fluxes as well as lake water quality. Here we analyse water quality data, recorded between 2006 and 2014 in 862 freshwater lakes in four geographical regions of China, to assess the input of phosphorus from human activity. We find that improvements in sanitation of both rural and urban domestic wastewater have resulted in large-scale declines in lake phosphorus concentrations in the most populated parts of China. In more sparsely populated regions, diffuse sources such as aquaculture and livestock farming offset this decline. Anthropogenic deforestation and soil erosion may also offset decreases in point sources of pollution. In the light of these regional differences, we suggest that a spatially flexible set of policies for water quality control would be beneficial for the future health of Chinese lakes.
Rivas, T; Pozo, S; Paz, M
2014-06-01
We describe the results of sulphur and oxygen isotope analyses used to identify sources of the gypsum present in black crusts that grow on the granite of historical buildings. The crusts were sampled at various locations in and near the city of Vigo (NW Spain) and were analysed for their sulphur content and δ(34)S and δ(18)O isotope ratios. Sampled crusts had δ(34)S values of 7.3‰ to 12.9‰ and δ(18)O values of 6.56‰ to 12.51‰. Sampled as potential sulphur sources were bulk depositions, seawater, foundation, ashlar and construction materials and combustion residues. The results indicated marine and, to a lesser extent, anthropogenic, origins for the sulphur and ruled out the contribution of sub-soil sulphates by capillary rise from building foundations. Isotope analyses would indicate that cement and mortar were enriched in sulphur after their application in buildings. The fact that facade orientation (towards the sea or fossil fuel pollution sources) was correlated with sulphur isotope distribution pointed to various contributions to black crust formation. Copyright © 2014 Elsevier B.V. All rights reserved.
2015-01-01
Targeted environmental monitoring reveals contamination by known chemicals, but may exclude potentially pervasive but unknown compounds. Marine mammals are sentinels of persistent and bioaccumulative contaminants due to their longevity and high trophic position. Using nontargeted analysis, we constructed a mass spectral library of 327 persistent and bioaccumulative compounds identified in blubber from two ecotypes of common bottlenose dolphins (Tursiops truncatus) sampled in the Southern California Bight. This library of halogenated organic compounds (HOCs) consisted of 180 anthropogenic contaminants, 41 natural products, 4 with mixed sources, 8 with unknown sources, and 94 with partial structural characterization and unknown sources. The abundance of compounds whose structures could not be fully elucidated highlights the prevalence of undiscovered HOCs accumulating in marine food webs. Eighty-six percent of the identified compounds are not currently monitored, including 133 known anthropogenic chemicals. Compounds related to dichlorodiphenyltrichloroethane (DDT) were the most abundant. Natural products were, in some cases, detected at abundances similar to anthropogenic compounds. The profile of naturally occurring HOCs differed between ecotypes, suggesting more abundant offshore sources of these compounds. This nontargeted analytical framework provided a comprehensive list of HOCs that may be characteristic of the region, and its application within monitoring surveys may suggest new chemicals for evaluation. PMID:25526519
Qiao, Min; Cai, Chao; Huang, Yizong; Liu, Yunxia; Lin, Aijun; Zheng, Yuanming
2011-01-01
Soil in metropolitan region suffers great contamination risk due to the rapid urbanization especially in developing countries. Beijing and Tianjin, together with their surrounding regions, form a mega-metropolitan region in northern China. To assess the soil environmental quality, a total of 458 surface soil samples were collected from this area. Concentrations of Cr, Cu, Pb, Zn, As, Cd, and Hg were analyzed and compared to the Chinese environmental quality standards for soil. Multivariate analysis was carried out to identify the possible sources and Geographic Information Systems techniques were applied to visualize the spatial data. It was found that the primary inputs of As were due to pedogenic sources, whereas Hg was mainly of anthropogenic source. Other elements including Cr, Cu, Pb, Zn, and Cd were from both lithogenic and anthropogenic origins. Health risk assessment based on the maximum heavy metal concentration indicated that As derived from sewage irrigation area can result in carcinogenic lifetime risk due to ingestion and/or dermal contact of soil. The potential non-carcinogenic risk for children is significant for Pb and the cumulative effect of multiple metals is of concern for children in the vicinity of mining site. The results increased our knowledge for understanding natural and anthropogenic sources as well as health risk for metals in metropolitan soil.
Reimann, Clemens; Arnoldussen, Arnold; Boyd, Rognvald; Finne, Tor Erik; Koller, Friedrich; Nordgulen, Øystein; Englmaier, Peter
2007-05-15
Forty samples each of leaves of birch (Betula pubescens Ehrh.), European mountain ash (Sorbus aucuparia (L.)) and bracken fern (Pteridium aquilinum (L.) Kuhn) as well as spruce needles (Picea abies (L.) Karsten) were collected along a 120 km south-north transect running through Norway's largest city, Oslo. Concentrations of 25 chemical elements (Ag, Au, B, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, La, Mg, Mn, Mo, Na, Ni, P, Pb, S, Sb, Sr, Ti, and Zn) as well as loss on ignition for the 4 sample materials are reported. The decline of input of sea spray with distance from the coast, geology, pH and anthropogenic contamination all played a role for the observed element concentrations in the leaves. Although growing under exactly the same natural conditions each plant species displayed quite unique uptake characteristics. Plant-species dependency and individual differences in the reaction of the plant leaves to different element sources make the investigated species of very limited value as bioindicators of anthropogenic activities. Anthropogenic contamination influences plant-leaf element content within a limited distance ( approximately 20 km) from the source.
NASA Astrophysics Data System (ADS)
Bauer, J. E.; Hossler, K.
2012-12-01
Riverine exports of carbon (C) and organic matter (OM) are regulated by a variety of natural and anthropogenic factors. Understanding the relationships between these various factors and C and OM exports can help to constrain global C budgets, as well allow assessment of current and future anthropogenic impacts on both riverine and global C cycles. We quantified the effects of multiple natural and anthropogenic controls on riverine export fluxes and compositions of particulate organic C (POC), dissolved organic C (DOC), and dissolved inorganic C (DIC) for a regional group of eight rivers in the northeastern U.S. For allochthonous and aged C contributions to POC, DOC and DIC exports, we first estimated fractional contributions from six potential sources for POC and DOC (i.e., modern C3 plant material (C3-OC), modern C4 plant material (C4-OC), modern algal material (algal OC), slow-turnover soil OC (slow SOC; turnover time 25 yr), passive-turnover soil OC (passive SOC; turnover time 5,000 yr) and fossil OC and four potential sources for DIC (i.e., modern atmospheric CO2 exchange, carbonate dissolution, POC remineralization and DOC remineralization) using a novel time-varying isotope mixing model. Using these estimated source contributions, we then estimated the allochthonous proportions of (a) the POC and DOC pools to be the C3-OC, C4-OC, slow SOC, passive SOC, and fossil OC contributions; and (b) the DIC pools to be the dissolved carbonates, remineralized allochthonous POC, and remineralized allochthonous DOC contributions. We considered aged C to be anything older than ˜ 60 yr, which included passive SOC and fossil OC for POC and DOC and dissolved carbonates and aged fractions of remineralized POC and DOC for DIC. Potential controls related to hydrogeomorphology and regional climate, soil order, soil texture, bedrock lithology, land use, and additional anthropogenic factors were analyzed collectively, individually, and at scales of both local and regional influence. Factors related either to hydrogeomorphology and climate or to anthropogenic factors exhibited the strongest impacts on riverine C exports and compositions, particularly at broader regional scales. The effect of hydrogeomorphology and climate was primarily one of size, as larger watersheds with greater discharge exported more total C and terrestrial C. Principal anthropogenic factors included impacts of wastewater treatment plants (WWTPs) and river impoundments. The presence of WWTPs as well as anthropogenic use of carbonate-based materials (e.g., limestone) may have substantially increased riverine C exports, particularly fossil C exports, in the study region. The presence of nuclear power plants in the associated watersheds is also discussed because of the potential for anthropogenic 14C inputs and subsequent biasing of aquatic C studies utilizing natural abundance 14C.
Bourbonnais, Mathieu L; Nelson, Trisalyn A; Cattet, Marc R L; Darimont, Chris T; Stenhouse, Gordon B
2013-01-01
Non-invasive measures for assessing long-term stress in free ranging mammals are an increasingly important approach for understanding physiological responses to landscape conditions. Using a spatially and temporally expansive dataset of hair cortisol concentrations (HCC) generated from a threatened grizzly bear (Ursus arctos) population in Alberta, Canada, we quantified how variables representing habitat conditions and anthropogenic disturbance impact long-term stress in grizzly bears. We characterized spatial variability in male and female HCC point data using kernel density estimation and quantified variable influence on spatial patterns of male and female HCC stress surfaces using random forests. Separate models were developed for regions inside and outside of parks and protected areas to account for substantial differences in anthropogenic activity and disturbance within the study area. Variance explained in the random forest models ranged from 55.34% to 74.96% for males and 58.15% to 68.46% for females. Predicted HCC levels were higher for females compared to males. Generally, high spatially continuous female HCC levels were associated with parks and protected areas while low-to-moderate levels were associated with increased anthropogenic disturbance. In contrast, male HCC levels were low in parks and protected areas and low-to-moderate in areas with increased anthropogenic disturbance. Spatial variability in gender-specific HCC levels reveal that the type and intensity of external stressors are not uniform across the landscape and that male and female grizzly bears may be exposed to, or perceive, potential stressors differently. We suggest observed spatial patterns of long-term stress may be the result of the availability and distribution of foods related to disturbance features, potential sexual segregation in available habitat selection, and may not be influenced by sources of mortality which represent acute traumas. In this wildlife system and others, conservation and management efforts can benefit by understanding spatial- and gender-based stress responses to landscape conditions.
Bourbonnais, Mathieu L.; Nelson, Trisalyn A.; Cattet, Marc R. L.; Darimont, Chris T.; Stenhouse, Gordon B.
2013-01-01
Non-invasive measures for assessing long-term stress in free ranging mammals are an increasingly important approach for understanding physiological responses to landscape conditions. Using a spatially and temporally expansive dataset of hair cortisol concentrations (HCC) generated from a threatened grizzly bear (Ursus arctos) population in Alberta, Canada, we quantified how variables representing habitat conditions and anthropogenic disturbance impact long-term stress in grizzly bears. We characterized spatial variability in male and female HCC point data using kernel density estimation and quantified variable influence on spatial patterns of male and female HCC stress surfaces using random forests. Separate models were developed for regions inside and outside of parks and protected areas to account for substantial differences in anthropogenic activity and disturbance within the study area. Variance explained in the random forest models ranged from 55.34% to 74.96% for males and 58.15% to 68.46% for females. Predicted HCC levels were higher for females compared to males. Generally, high spatially continuous female HCC levels were associated with parks and protected areas while low-to-moderate levels were associated with increased anthropogenic disturbance. In contrast, male HCC levels were low in parks and protected areas and low-to-moderate in areas with increased anthropogenic disturbance. Spatial variability in gender-specific HCC levels reveal that the type and intensity of external stressors are not uniform across the landscape and that male and female grizzly bears may be exposed to, or perceive, potential stressors differently. We suggest observed spatial patterns of long-term stress may be the result of the availability and distribution of foods related to disturbance features, potential sexual segregation in available habitat selection, and may not be influenced by sources of mortality which represent acute traumas. In this wildlife system and others, conservation and management efforts can benefit by understanding spatial- and gender-based stress responses to landscape conditions. PMID:24386273
Yeager, Lauren A; Marchand, Philippe; Gill, David A; Baum, Julia K; McPherson, Jana M
2017-07-01
Biophysical conditions, including climate, environmental stress, and habitat availability, are key drivers of many ecological processes (e.g., community assembly and productivity) and associated ecosystem services (e.g., carbon sequestration and fishery production). Furthermore, anthropogenic impacts such as coastal development and fishing can have drastic effects on the structure and function of marine ecosystems. Scientists need to account for environmental variation and human impacts to accurately model, manage, and conserve marine ecosystems. Although there are many types of environmental data available from global remote sensing and open-source data products, some are inaccessible to potential end-users because they exist as global layers in high temporal and spatial resolutions which require considerable computational power to process. Additionally, coastal locations often suffer from missing data or data quality issues which limit the utility of some global marine products for coastal sites. Herein we present the Marine Socio-Environmental Covariates dataset for the global oceans, which consists of environmental and anthropogenic variables summarized in ecologically relevant ways. The dataset includes four sets of environmental variables related to biophysical conditions (net primary productivity models corrected for shallow-water reflectance, wave energy including sheltered-coastline corrections) and landscape context (coral reef and land cover within varying radii). We also present two sets of anthropogenic variables, human population density (within varying radii) and distance to large population center, which can serve as indicators of local human impacts. We have paired global, summarized layers available for download with an online data querying platform that allows users to extract data for specific point locations with finer control of summary statistics. In creating these global layers and online platform, we hope to make the data accessible to a wide array of end-users with the goal of advancing marine ecosystem studies. © 2017 by the Ecological Society of America.
Identification of tsunami deposits using organic markers
NASA Astrophysics Data System (ADS)
Bellanova, Piero; Schwarzbauer, Jan; Reicherter, Klaus; Jaffe, Bruce; Szczucinski, Witold
2017-04-01
Geochemical analyses of tsunami deposits are becoming standard and are used in almost every study. However, only inorganic proxies are typically studied. Recent studies that developed and broaden geochemical methods to investigate tsunami deposits (e.g., Szczucinski et al., 2016) and illustrate the importance of information from biomarker analyses (e.g., Shinozaki et al., 2015). These studies indicated that organic geochemistry can be used for the differentiation between marine and terrestrial matter, indicating a potential source of a deposit. Organic proxies also have the advantage of remaining longer in the sediment than inorganic proxies, which can be leached out by groundwater or rain. The 2011 Tohoku-oki tsunami inundated as much as 4.5 km inland and had run up heights of up to 40 m. Samples of sandy tsunami deposits from Sendai Plain, Samenoura Bay, and Oppa Bay (Japan) were collected and analyzed using gas chromatography-mass spectrometry (GC-MS) to search for natural compounds (biomarkers) and anthropogenic pollutants (anthropogenic markers). Natural compounds substances, such as fatty acids and n-alkanes, and anthropogenic compounds (e.g., polycyclic aromatic hydrocarbons and pesticides) were identified and quantified. Further, the two different compound types (natural vs. anthropogenic) were evaluated for their usefulness in identification of deposits from extreme flooding events. The analyzed chemical compounds and their diagenetic transformation products were distinctly different for the pre-tsunami, the tsunami and the thin post-tsunami eolian deposits. The preliminary results of this study point out the utility of organic indicators for the identification of extreme flooding events (like tsunamis), particularly for historic events. References Shinozaki, T., Fujino, S., Ikehara, M., Sawai, Y., Tamura, T., Goto, K., Sugawara, D., Abe, T., 2015. Marine biomarkers deposited on coastal land by the 2011Tohoku-oki tsunami. Natural Hazards 77,455-460. Szczuciński, W., Pawłowska, J., Lejzerowicz, F., Nishimura, Y., Kokociński, M., Majewski, W., Nakamura, Y., Pawlowski, J., 2016. Ancient sedimentary DNA reveals past tsunami deposits. Marine Geology 381, 29-33.
Okuda, Tomoaki; Katsuno, Masayuki; Naoi, Daisuke; Nakao, Shunsuke; Tanaka, Shigeru; He, Kebin; Ma, Yongliang; Lei, Yu; Jia, Yingtao
2008-06-01
Daily observations of hazardous trace metal concentrations in aerosols in Beijing, China were made in the period from 2001 to 2006. We considered coal combustion as a major source of some anthropogenic metals by achieving a correlation analysis and by investigating enrichment factors and relative composition of metals. A possible extra source of some specific metals, such as Cu and Sb, was brake abrasion particles, however, we did not think the transport-related particle was a major source for the hazardous anthropogenic metals even though they could originate from vehicle exhaust and brake/tire abrasion particles. A time-trend model was used to describe temporal variations of chemical constituent concentrations during the five-year period. Several crustal elements, such as Al, Ti, V, Cr, Mn, Fe, and Co, did not show clear increases, with annual rates of change of -15.2% to 3.6%. On the other hand, serious increasing trends were noted from several hazardous trace metals. Cu, Zn, As, Cd, and Pb, which are derived mainly from anthropogenic sources, such as coal combustion, showed higher annual rate of change (4.9-19.8%, p<0.001) according to the regression model. In particular, the Cd and Pb concentrations increased remarkably. We hypothesize that the trend towards increasing concentrations of metals in the air reflects a change that has occurred in the process of burning coal, whereby the use of higher temperatures for coal combustion has resulted in increased emissions of these metals. The increasing use of low-rank coal may also explain the observed trends. In addition, nonferrous metal smelters are considered as a potential, albeit minor, reason for the increasing atmospheric concentrations of anthropogenic hazardous metals in Beijing city.
Tracing geogenic and anthropogenic sources in urban dusts: Insights from lead isotopes
NASA Astrophysics Data System (ADS)
Del Rio-Salas, R.; Ruiz, J.; De la O-Villanueva, M.; Valencia-Moreno, M.; Moreno-Rodríguez, V.; Gómez-Alvarez, A.; Grijalva, T.; Mendivil, H.; Paz-Moreno, F.; Meza-Figueroa, D.
2012-12-01
Tracing the source of metals in the environment is critical to understanding their pollution level and fate. Geologic materials are an important source of airborne particulate matter, but the contribution of contaminated soil to concentrations of Pb in airborne dust is not yet widely documented. To examine the potential significance of this mechanism, surface soil samples were collected, as well as wind-transported dust trapped at 1 and 2 m height at seven different locations including residential, industrial, high-traffic and rural sites. Samples of dust deposited on roofs from 24 schools were also obtained and analyzed for Pb isotope ratios. Spatial distribution of Pb of airborne and sedimented dust suggests a process dominated by re-suspension/sedimentation, which was controlled by erosion, traffic and topography of the urban area. Anthropogenic lead input in the city grades outward the urban zone toward geogenic values. Our results shows that Pb-isotopic signatures of leaded gasoline are imprinted in dust sedimented on roofs. Considering that leaded-gasoline has not been in use in Mexico since two decades ago, this signature shows not only a Pb-legacy in soil, but also a re-suspension process affecting air column below 3 m in height. The combination of the 207Pb/206Pb data of the surrounding rocks and urban dust, reveal three well-defined zones with remarkable anthropogenic influence, which correspond to the oldest urban sectors. This work highlights the importance of spatial characterization of metals in particles suspended below a height of 3 m of the airborne column, a fact that should be considered to identify exposure paths to humans and the potential risks. Lead isotope signatures allowed the identification of geogenic and anthropogenic emission sources for dust, a matter that deserves consideration in the efforts to control airborne metal emissions.
A geochemical study of overbank sediments in an urban area (Madrid, Spain).
Adánez Sanjuán, Paula; Llamas Borrajo, Juan F; Locutura Rupérez, Juan; García Cortés, Angel
2014-12-01
Overbank and stream sediments have been studied in the Community of Madrid. Four vertical profiles have been sampled corresponding to Guadarrama, Jarama, and finally Manzanares River, where two profiles have been studied upstream (El Pardo profile) and downstream (Rivas profile) Madrid city. Sieved samples (<63 µm) were subjected to total (ICP-MS/ICP-OES and INAA) and partial analysis (ICP-MS). AMS radiocarbon dating techniques revealed a young age (170 ± 40 years BP) at 2.40-2.65 m depth for Rivas profile. It has not been possible to detect pristine or pre-industrial overbank sediments, since in the rest of the studied profiles, anthropogenic wastes were found even in the lower levels. Three main sources of sediment have been detected in the area. Granitic and arkosic geology, located in the northern part of Madrid (U, Th, W, K, Na, or rare earth elements); clays located in the southeast of Madrid (Ni, Cr, or V), and finally an anthropogenic source has been identified (Au, Ag, Pb, Zn, or Sb) in Rivas profile. The influence of the anthropogenic activity has been established based on the contents distribution of contaminant elements in the profile. This can be associated to the growth of industrial activities and population in the city of Madrid during the last decades. The comparison of the profiles by a k-means cluster analysis showed some similarities for these samples that could have analogous sources (anthropogenic and geological).
Kang, Xuming; Song, Jinming; Yuan, Huamao; Duan, Liqin; Li, Xuegang; Li, Ning; Liang, Xianmeng; Qu, Baoxiao
2017-09-01
Heavy metal contamination is an essential indicator of environmental health. In this work, one sediment core was used for the analysis of the speciation of heavy metals (Cr, Mn, Ni, Cu, Zn, As, Cd, and Pb) in Jiaozhou Bay sediments with different grain sizes. The bioavailability, sources and ecological risk of heavy metals were also assessed on a centennial timescale. Heavy metals were enriched in grain sizes of < 63µm and were predominantly present in residual phases. Moreover, the mobility sequence based on the sum of the first three phases (for grain sizes of < 63µm) was Mn > Pb > Cd > Zn > Cu >Ni > Cr > As. Enrichment factors (EF) indicated that heavy metals in Jiaozhou Bay presented from no enrichment to minor enrichment. The potential ecological risk index (RI) indicated that Jiaozhou Bay had been suffering from a low ecological risk and presented an increasing trend since 1940s owing to the increase of anthropogenic activities. The source analysis indicated that natural sources were primary sources of heavy metals in Jiaozhou Bay and anthropogenic sources of heavy metals presented an increasing trend since 1940s. The principal component analysis (PCA) indicated that Cr, Mn, Ni, Cu and Pb were primarily derived from natural sources and that Zn and Cd were influenced by shipbuilding industry. Mn, Cu, Zn and Pb may originate from both natural and anthropogenic sources. As may be influenced by agricultural activities. Moreover, heavy metals in sediments of Jiaozhou Bay were clearly influenced by atmospheric deposition and river input. Copyright © 2017. Published by Elsevier Inc.
Using Model Comparisons to Understand Sources of Nitrogen Delivered to US Coastal Areas
Nitrogen loading to water bodies can result in eutrophication-related hypoxia and degraded water quality. The relative contributions of different anthropogenic and natural sources of in-stream N cannot be directly measured at whole-watershed scales; hence, N source attribution e...
NASA Astrophysics Data System (ADS)
Kamenov, George D.; Brenner, Mark; Tucker, Jaimie L.
2009-06-01
Analysis of a well-dated peat core from Blue Cypress Marsh (BCM) provides a detailed record of natural and anthropogenic factors that controlled the geochemical cycles of a number of trace elements in Florida over the last five centuries. The trace elements were divided into "natural" and "anthropogenic" groups using concentration trends from the bottom to the top of the core. The "natural" group includes Li, Sc, Cr, Co, Ga, Ge, Zr, Nb, Cs, Ba, Hf, Y, Ta, Th, and REE (Rare Earth Elements). These elements show similar concentrations throughout the core, indicating that changes in human activities after European arrival in the "New World" did not affect their geochemical cycles. The "anthropogenic" group includes Pb, Cu, Zn, V, Sb, Sn, Bi, and Cd. Upcore enrichment of these elements indicates enhancement by anthropogenic activities. From the early 1500s to present, fluxes of the "anthropogenic" metals to the marsh increased significantly, with modern accumulation rates several-fold (e.g., V) to hundreds of times (e.g., Zn) greater than pre-colonial rates. The dominant input mechanism for trace elements from both groups to the marsh has been atmospheric deposition. Atmospheric input of a number of the elements, including the anthropogenic metals, was dominated by local sources during the last century. For several elements, long-distant transport may be important. For instance, REE and Nd isotopes provide evidence for long-range atmospheric transport dominated by Saharan dust. The greatest increase in flux of the "anthropogenic" metals occurred during the 20th century and was caused by changes in the chemical composition of atmospheric deposition entering the marsh. Increased atmospheric inputs were a consequence of several anthropogenic activities, including fossil fuel combustion (coal and oil), agricultural activities, and quarrying and mining operations. Pb and V exhibit similar trends, with peak accumulation rates in 1970. The principal anthropogenic source of V is oil combustion. The decline in V accumulation after 1970 in the BCM peat corresponds to the introduction of low-sulfur fuels and the change from heavy to distilled oils since the 1970s. After the 1920s, Pb distribution in the peat follows closely the history of alkyl lead consumption in the US, which peaked in the 1970s. Pb isotopes support this inference and furthermore, record changes in the ore sources used to produce leaded gasoline. Idaho ores dominated the peat Pb isotope record until the 1960s, followed by Pb from Mississippi Valley Type deposits from the 1960s to the 1980s. Enhanced fluxes of Cu, Zn, Cd, Sn, Sb, Bi, and to some extent Ni during the last century are likely also related to fossil fuel combustion. Local agricultural activities may also have influenced the geochemical cycles of Cu and Zn. The peat record shows enhanced U accumulation during the last century, possibly related to phosphate mining in western Florida. Sr isotopes in the peat core also reflect anthropogenic influence. The 87Sr/ 86Sr ratio decreases from natural background values in the basal part of the core to lower values in the upper part of the core. The Sr isotope shift is probably related to quarrying operations in Florida, and marks the first time an anthropogenic signal has been detected using the Sr isotope record in a peat core.
Analysis of SO II point source emissions using NASA atmospheric infrared sounder data
NASA Astrophysics Data System (ADS)
Shen, Sylvia S.; Miller, David P.; Lewis, Paul E.
2007-04-01
Determining the extent to which large power plant emission sources interacting with atmospheric constituents affect the environment could play a significant role in future U.S. energy production policy. The effects on the environment caused by the interaction between power plant emissions and atmospheric constituents has not been investigated in depth due to the lack of calibrated spectral data on a suitable temporal and spatial scale. The availability of NASA's space-based Atmospheric Infrared Sounder (AIRS) data makes it possible to explore, and begin the first steps toward establishing, a correlation between known emission sources and environmental indicators. An exploratory study was conducted in which a time series of 26 cloud-free AIRS data containing two coal-fired power plants in northern New Mexico were selected, acquired, and analyzed for SO II emissions. A generic forward modeling process was also developed to derive an estimate of the expected AIRS pixel radiance containing the SO II emissions from the two power plants based on published combustion analysis data for coal and available power plant documentation. Analysis of the AIRS NEΔR calculated in this study and subsequent comparison with the radiance values for SO II calculated from the forward model provided essential information regarding the suitability and risk in the use of a modified AIRS configuration for monitoring anthropogenic point source emissions. The results of this study along with its conclusions and recommendations in conjunction with additional research collaboration in several specific topics will provide guidance for the development of the next generation infrared spectrometer system that NASA is considering building for environmental monitoring.
An Assessment of Fine Particulate (PM2.5) Air Pollution in Jeddah, Saudi Arabia
NASA Astrophysics Data System (ADS)
Nayebare, S. R.; Khwaja, H. A.; Aburizaiza, O. S.; Siddique, A.; Zeb, J.; Hussain, M. M.; Khatib, F.; Blake, D. R.; Carpenter, D. O.
2017-12-01
We assessed the levels, chemical composition and delineated the sources of PM2.5 in Jeddah, to estimate the anthropogenic influence. Sampling was done from April 8th 2013 to February 18th, 2014 in four cycles. PM2.5 samples were analyzed for black carbon (BC), trace elements (TEs) and water-soluble ionic species (IS). Delineation of sources was by mass reconstruction, enrichment factor (EF), and positive matrix factorization (PMF). The 24-h PM2.5 levels showed seasonal variabilities with mean PM2.5 per cycle (cycle 1: 58.8±25.0, cycle 2: 36.2±12.3, cycle 3: 33.9±9.1, and cycle 4: 38.0±17.7µg/m3) exceeding the WHO guideline (25.0 µg/m3). Overall, BC explained 3.61%, 5.92%, 7.15% and 6.51% of PM2.5 during cycles 1-4, respectively but with delta-C levels below zero. This excluded bio-mass burning as a PM2.5 source. IS were mostly SO42-, NO3-, NH4+, Na+ and K+, characteristic of industrial and vehicular emissions. From mass reconstruction, BC, TEs and IS collectively explained 73.6 - 89.5% of PM2.5. EF analysis defined two broad categories of TEs as; anthropogenic (Ni, V, Cu, Zn, Cl, Pb, S, Lu and Br), and earth-crust derived (Al, Si, Ti, Mg, K, Fe, Sr, Mn, Ca, Na and Cr) TEs. These anthropogenic TEs are mostly of industrial and vehicular origins. PMF broadly defined 4 major sources of PM2.5; fossil fuels combustion (36.0%), soil (34.1%), sea-spray (15.4%) and vehicular emissions (14.5%). Results show a major anthropogenic influence related to vehicular and industrial emissions, and further stress the need for more research to fully delineate PM2.5 sources in Jeddah.
Gwenzi, Willis; Mangori, Lynda; Danha, Concilia; Chaukura, Nhamo; Dunjana, Nothando; Sanganyado, Edmond
2018-04-26
Recent studies show that high-technology rare earth elements (REEs) of anthropogenic origin occur in the environment including in aquatic systems, suggesting REEs are contaminants of emerging concern. However, compared to organic contaminants, there is a lack of comprehensive reviews on the anthropogenic sources, environmental behaviour, and public and ecological health risks of REEs. The current review aims to: (1) identify anthropogenic sources, transfer mechanisms, and environmental behaviour of REEs; (2) highlight the human and ecological health risks of REEs and propose mitigation measures; and (3) identify knowledge gaps and future research directions. Out of the 17 REEs, La, Gd, Ce and Eu are the most studied. The main sources of anthropogenic REE include; medical facilities, petroleum refining, mining and technology industries, fertilizers, livestock feeds, and electronic wastes and recycling plants. REEs are mobilized and transported in the environment by hydrological and wind-driven processes. Ecotoxicological effects include reduced plant growth, function and nutritional quality, genotoxicity and neurotoxicity in animals, trophic bioaccumulation, chronic and acute toxicities in soil organisms. Human exposure to REEs occurs via ingestion of contaminated water and food, inhalation, and direct intake during medical administration. REEs have been detected in human hair, nails, and biofluids. In humans, REEs cause nephrogenic systemic fibrosis and severe damage to nephrological systems associated with Gd-based contrast agents, dysfunctional neurological disorder, fibrotic tissue injury, oxidative stress, pneumoconiosis, cytotoxicity, anti-testicular effects, and male sterility. Barring REEs in medical devices, epidemiological evidence directly linking REEs in the environment to human health conditions remains weak. To minimize health risks, a conceptual framework and possible mitigation measures are highlighted. Future research is needed to better understand sources, environmental behaviour, ecotoxicology, and human epidemiology. Moreover, research on REEs in developing regions, including Africa, is needed given prevailing conditions predisposing humans to health risks (e.g., untreated drinking water). Copyright © 2018 Elsevier B.V. All rights reserved.
Determining provenance of marine metal pollution in French bivalves using Cd, Zn and Pb isotopes
NASA Astrophysics Data System (ADS)
Shiel, Alyssa E.; Weis, Dominique; Cossa, Daniel; Orians, Kristin J.
2013-11-01
Cadmium, Zn and Pb isotopic compositions (MC-ICP-MS) and elemental concentrations (HR-ICP-MS) have been used to distinguish between natural and anthropogenic sources of these metals in bivalves collected from the coastlines of France (English Channel, Atlantic and Mediterranean coasts). The Cd isotopic signatures (δ114Cd = -1.08‰ to -0.52‰) exhibited by bivalves from the coastlines of France, excluding those from NE France, are within the range of those exhibited by bivalves from the USA East coast (δ114Cd = -1.20‰ to -0.54‰). This indicates the high prevalence of industry, as well as the low natural contributions of Cd from North Atlantic waters in both regions. Thus, the significance of anthropogenic Cd sources is similar. These significant anthropogenic contributions are identified for bivalves with a large range in tissue Cd concentrations. Importantly, French bivalves from the Gironde estuary and Marennes-Oléron basin (regions of historic and modern importance for oyster farming, respectively) exhibited the highest Cd levels of the study. Their Cd isotopic signatures indicate historical smelting emissions remain the primary Cd source despite the cessation of local smelting activities in 1986 and subsequent remedial efforts. No significant variability is observed in the δ66Zn values of the French bivalves (∼0.53‰), with the exception of the much heavier compositions exhibited by oysters from the polluted Gironde estuary (1.19-1.27‰). Lead isotopes do not fractionate during processing like Cd and Zn. They can, therefore, be used to identify emissions from industrial processes and the consumption of unleaded gasoline and diesel fuel as metal sources to French bivalves. Cadmium and Zn isotopes are successfully used here as tracers of anthropogenic processing emissions and are combined with Pb isotope "fingerprinting" techniques to identify metal sources.
Botelho, Maria João; Soares, Florbela; Matias, Domitília; Vale, Carlos
2015-07-15
The clam Ruditapes decussatus was transplanted from a natural recruitment area of Ria Formosa to three sites, surveyed for nutrients in water and sediments. Specimens were sampled monthly for determination of Escherichia coli, condition index and gonadal index. Higher nutrient values in low tide reflect drainage, anthropogenic sources or sediment regeneration, emphasising the importance of water mixing in the entire lagoon driven by the tide. Despite the increase of effluent discharges in summer due to tourism, nutrient concentrations and E. coli in clams were lower in warmer periods. The bactericide effect of temperature and solar radiation was better defined in clams from the inlet channel site than from sites closer to urban effluents. High temperature in summer and torrential freshwater inputs to Ria Formosa may anticipate climate change scenarios for south Europe. Seasonal variation of nutrients and clam contamination may thus point to possible alterations in coastal lagoons and their ecosystem services. Copyright © 2015. Published by Elsevier Ltd.
NASA Astrophysics Data System (ADS)
Dumont, E.; Harrison, J. A.; Kroeze, C.; Bakker, E. J.; Seitzinger, S. P.
2005-12-01
Here we describe, test, and apply a spatially explicit, global model for predicting dissolved inorganic nitrogen (DIN) export by rivers to coastal waters (NEWS-DIN). NEWS-DIN was developed as part of an internally consistent suite of global nutrient export models. Modeled and measured DIN export values agree well (calibration R2 = 0.79), and NEWS-DIN is relatively free of bias. NEWS-DIN predicts: DIN yields ranging from 0.0004 to 5217 kg N km-2 yr-1 with the highest DIN yields occurring in Europe and South East Asia; global DIN export to coastal waters of 25 Tg N yr-1, with 16 Tg N yr-1 from anthropogenic sources; biological N2 fixation is the dominant source of exported DIN; and globally, and on every continent except Africa, N fertilizer is the largest anthropogenic source of DIN export to coastal waters.
NASA Technical Reports Server (NTRS)
Chin, Mian; Ginoux, Paul; Dubovik, Oleg; Holben, Brent; Kaufman, Yoram; chu, Allen; Anderson, Tad; Quinn, Patricia
2003-01-01
Aerosol climate forcing is one of the largest uncertainties in assessing the anthropogenic impact on the global climate system. This uncertainty arises from the poorly quantified aerosol sources, especially black carbon emissions, our limited knowledge of aerosol mixing state and optical properties, and the consequences of intercontinental transport of aerosols and their precursors. Here we use a global model GOCART to simulate atmospheric aerosols, including sulfate, black carbon, organic carbon, dust, and sea salt, from anthropogenic, biomass burning, and natural sources. We compare the model calculated aerosol extinction and absorption with those quantities from the ground-based sun photometer measurements from AERONET at several different wavelengths and the field observations from ACE-Asia, and model calculated total aerosol optical depth and fine mode fractions with the MODIS satellite retrieval. We will also estimate the intercontinental transport of pollution and dust aerosols from their source regions to other areas in different seasons.
NASA Technical Reports Server (NTRS)
Chin, Mian; Chu, Allen; Levy, Robert; Remer, Lorraine; Kaufman, Yoram; Dubovik, Oleg; Holben, Brent; Eck, Tom; Anderson, Tad; Quinn, Patricia
2004-01-01
Aerosol climate forcing is one of the largest uncertainties in assessing the anthropogenic impact on the global climate system. This uncertainty arises from the poorly quantified aerosol sources, especially black carbon emissions, our limited knowledge of aerosol mixing state and optical properties, and the consequences of intercontinental transport of aerosols and their precursors. Here we use a global model GOCART to simulate atmospheric aerosols, including sulfate, black carbon, organic carbon, dust, and sea salt, from anthropogenic, .biomass burning, and natural sources. We compare the model calculated aerosol extinction and absorption with those quantities from the ground-based sun photometer measurements from AERON" at several different wavelengths and the field observations from ACE-Asia, and model calculated total aerosol optical depth and fine mode fractions with the MODIS satellite retrieval. We will also estimate the intercontinental transport of pollution and dust aerosols from their source regions to other areas in different seasons.
Detecting small scale CO2 emission structures using OCO-2
NASA Astrophysics Data System (ADS)
Schwandner, Florian M.; Eldering, Annmarie; Verhulst, Kristal R.; Miller, Charles E.; Nguyen, Hai M.; Oda, Tomohiro; O'Dell, Christopher; Rao, Preeti; Kahn, Brian; Crisp, David; Gunson, Michael R.; Sanchez, Robert M.; Ashok, Manasa; Pieri, David; Linick, Justin P.; Yuen, Karen
2016-04-01
Localized carbon dioxide (CO2) emission structures cover spatial domains of less than 50 km diameter and include cities and transportation networks, as well as fossil fuel production, upgrading and distribution infra-structure. Anthropogenic sources increasingly upset the natural balance between natural carbon sources and sinks. Mitigation of resulting climate change impacts requires management of emissions, and emissions management requires monitoring, reporting and verification. Space-borne measurements provide a unique opportunity to detect, quantify, and analyze small scale and point source emissions on a global scale. NASA's first satellite dedicated to atmospheric CO2 observation, the July 2014 launched Orbiting Carbon Observatory (OCO-2), now leads the afternoon constellation of satellites (A-Train). Its continuous swath of 2 to 10 km in width and eight footprints across can slice through coincident emission plumes and may provide momentary cross sections. First OCO-2 results demonstrate that we can detect localized source signals in the form of urban total column averaged CO2 enhancements of ~2 ppm against suburban and rural backgrounds. OCO-2's multi-sounding swath observing geometry reveals intra-urban spatial structures reflected in XCO2 data, previously unobserved from space. The transition from single-shot GOSAT soundings detecting urban/rural differences (Kort et al., 2012) to hundreds of soundings per OCO-2 swath opens up the path to future capabilities enabling urban tomography of greenhouse gases. For singular point sources like coal fired power plants, we have developed proxy detections of plumes using bands of imaging spectrometers with sensitivity to SO2 in the thermal infrared (ASTER). This approach provides a means to automate plume detection with subsequent matching and mining of OCO-2 data for enhanced detection efficiency and validation. © California Institute of Technology
NASA Astrophysics Data System (ADS)
White, Emily; Rigby, Matt; O'Doherty, Simon; Stavert, Ann; Lunt, Mark; Nemitz, Eiko; Helfter, Carole; Allen, Grant; Pitt, Joe; Bauguitte, Stéphane; Levy, Pete; van Oijen, Marcel; Williams, Mat; Smallman, Luke; Palmer, Paul
2016-04-01
Having a comprehensive understanding, on a countrywide scale, of both biogenic and anthropogenic CO2 emissions is essential for knowing how best to reduce anthropogenic emissions and for understanding how the terrestrial biosphere is responding to global fossil fuel emissions. Whilst anthropogenic CO2 flux estimates are fairly well constrained, fluxes from biogenic sources are not. This work will help to verify existing anthropogenic emissions inventories and give a better understanding of biosphere - atmosphere CO2 exchange. Using an innovative top-down inversion scheme; a hierarchical Bayesian Markov Chain Monte Carlo approach with reversible jump "trans-dimensional" basis function selection, we aim to find emissions estimates for biogenic and anthropogenic sources simultaneously. Our approach allows flux uncertainties to be derived more comprehensively than previous methods, and allows the resolved spatial scales in the solution to be determined using the data. We use atmospheric CO2 mole fraction data from the UK Deriving Emissions related to Climate Change (DECC) and Greenhouse gAs UK and Global Emissions (GAUGE) projects. The network comprises of 6 tall tower sites, flight campaigns and a ferry transect along the east coast, and enables us to derive high-resolution monthly flux estimates across the UK and Ireland for the period 2013-2015. We have derived UK total fluxes of 675 PIC 78 Tg/yr during January 2014 (seasonal maximum) and 23 PIC 96 Tg/yr during May 2014 (seasonal minimum). Our disaggregated anthropogenic and biogenic flux estimates are compared to a new high-resolution time resolved anthropogenic inventory that will underpin future UNFCCC reports by the UK, and to DALEC carbon cycle model. This allows us to identify where significant differences exist between these "bottom-up" and "top-down" flux estimates and suggest reasons for discrepancies. We will highlight the strengths and limitations of the UK's CO2 emissions verification infrastructure at present and outline improvements that could be made in the future.
Kathryn L. Purcell; Scott L. Stephens
2005-01-01
Fire was once an important component of the disturbance regime in oak woodlands of the Sierra Nevada foothills. In addition to lightning-ignited fires, anthropogenic sources of ignition have historically been important until fire suppression activities in the mid- 20th century lengthened fire return intervals. Few fire history studies have addressed oak woodlands, and...
Stephen M. Ogle; Grant Domke; Werner A. Kurz; Marcelo T. Rocha; Ted Huffman; Amy Swan; James E. Smith; Christopher Woodall; Thelma Krug
2018-01-01
Land use and management activities have a substantial impact on carbon stocks and associated greenhouse gas emissions and removals. However, it is challenging to discriminate between anthropogenic and non-anthropogenic sources and sinks from land. To address this problem, the Intergovernmental Panel on Climate Change developed a managed land proxy to determine which...
NASA Astrophysics Data System (ADS)
Lee, K.; Ko, Y. H.; Moon, J. Y.
2017-12-01
The relative abundance of nitrate (N) over phosphorus (P) has increased significantly over the period since 1980 in the marginal seas (Yellow, East China and East seas) bordering the northwestern Pacific Ocean, located downstream of the populated and industrialized Asian continent. Analysis of datasets for anthropogenic N input, satellite chlorophyll-a (Chl-a), and seawater nutrient data ( 200,000 data points) reveal that transport of N originating from China has been responsible for enhancements of Chl-a in the marginal seas of the northwestern Pacific Ocean. In particular, the contribution of anthropogenic N to new production in these marginal seas is expected to grow considerably in the coming decades. This anthropogenically driven increase in the N content may potentially lead to a long-term change of these marginal seas from being N-limited to P-limited.
Specific storage volumes: A useful tool for CO2 storage capacity assessment
Brennan, S.T.; Burruss, R.C.
2006-01-01
Subsurface geologic strata have the potential to store billions of tons of anthropogenic CO2; therefore, geologic carbon sequestration can be an effective mitigation tool used to slow the rate at which levels of atmospheric CO2 are increasing. Oil and gas reservoirs, coal beds, and saline reservoirs can be used for CO2 storage; however, it is difficult to assess and compare the relative storage capacities of these different settings. Typically, CO2 emissions are reported in units of mass, which are not directly applicable to comparing the CO2 storage capacities of the various storage targets. However, if the emission values are recalculated to volumes per unit mass (specific volume) then the volumes of geologic reservoirs necessary to store CO2 emissions from large point sources can be estimated. The factors necessary to convert the mass of CO2 emissions to geologic storage volume (referred to here as Specific Storage Volume or 'SSV') can be reported in units of cubic meters, cubic feet, and petroleum barrels. The SSVs can be used to estimate the reservoir volume needed to store CO2 produced over the lifetime of an individual point source, and to identify CO2 storage targets of sufficient size to meet the demand from that given point source. These storage volumes also can then be projected onto the land surface to outline a representative "footprint," which marks the areal extent of storage. This footprint can be compared with the terrestrial carbon sequestration capacity of the same land area. The overall utility of this application is that the total storage capacity of any given parcel of land (from surface to basement) can be determined, and may assist in making land management decisions. ?? Springer Science+Business Media, LLC 2006.
The relative contributions of different anthropogenic and natural sources of in-stream nitrogen (N) cannot be directly measured at whole-watershed scales. Hence, source attribution estimates beyond the scale of small catchments must rely on models. Although such estimates have be...
Sources of reactive nitrogen in marine aerosol over the Northwest Pacific Ocean in spring
NASA Astrophysics Data System (ADS)
Luo, Li; Kao, Shuh-Ji; Bao, Hongyan; Xiao, Huayun; Xiao, Hongwei; Yao, Xiaohong; Gao, Huiwang; Li, Jiawei; Lu, Yangyang
2018-05-01
Atmospheric deposition of long-range transport of anthropogenic reactive nitrogen (Nr, mainly comprised of NHx, NOy and water-soluble organic nitrogen, WSON) from continents may have profound impact on marine biogeochemistry. In addition, surface ocean dissolved organic nitrogen (DON) may also contribute to aerosol WSON in the overlying atmosphere. Despite the importance of off-continent dispersion and Nr interactions at the atmosphere-ocean boundary, our knowledge of the sources of various nitrogen species in the atmosphere over the open ocean remains limited due to insufficient observations. We conducted two cruises in the spring of 2014 and 2015 from the coast of China through the East China seas (ECSs, i.e. the Yellow Sea and East China Sea) to the open ocean (i.e. the Northwest Pacific Ocean, NWPO). Concentrations of water-soluble total nitrogen (WSTN), NO3- and NH4+, as well as the δ15N of WSTN and NO3- in marine aerosol, were measured during both cruises. In the spring of 2015, we also analysed the concentrations and δ15N of NO3- and the DON of surface seawater (SSW; at a depth of 5 m) along the cruise track. Aerosol NO3-, NH4+ and WSON decreased logarithmically (1-2 orders of magnitude) with distance from the shore, reflecting strong anthropogenic emission sources of NO3-, NH4+ and WSON in China. Average aerosol NO3- and NH4+ concentrations were significantly higher in 2014 (even in the remote NWOP) than in 2015 due to the stronger wind field in 2014, underscoring the role of the Asian winter monsoon in the seaward transport of anthropogenic NO3- and NH4+. However, the background aerosol WSON over the NWPO in 2015 (13.3 ± 8.5 nmol m-3) was similar to that in 2014 (12.2 ± 6.3 nmol m-3), suggesting an additional non-anthropogenic WSON source in the open ocean. Obviously, marine DON emissions should be considered in model and field assessments of net atmospheric WSON deposition in the open ocean. This study contributes information on parallel isotopic marine DON composition and aerosol Nr datasets, but more research is required to explore complex Nr sources and deposition processes in order to advance our understanding of anthropogenic influences on the marine nitrogen cycle and nitrogen exchange at land-ocean and atmosphere-ocean interfaces.
Monitoring of PM10 and PM2.5 around primary particulate anthropogenic emission sources
NASA Astrophysics Data System (ADS)
Querol, Xavier; Alastuey, Andrés; Rodriguez, Sergio; Plana, Felicià; Mantilla, Enrique; Ruiz, Carmen R.
Investigations on the monitoring of ambient air levels of atmospheric particulates were developed around a large source of primary anthropogenic particulate emissions: the industrial ceramic area in the province of Castelló (Eastern Spain). Although these primary particulate emissions have a coarse grain-size distribution, the atmospheric transport dominated by the breeze circulation accounts for a grain-size segregation, which results in ambient air particles occurring mainly in the 2.5-10 μm range. The chemical composition of the ceramic particulate emissions is very similar to the crustal end-member but the use of high Al, Ti and Fe as tracer elements as well as a peculiar grain-size distribution in the insoluble major phases allow us to identify the ceramic input in the bulk particulate matter. PM2.5 instead of PM10 monitoring may avoid the interference of crustal particles without a major reduction in the secondary anthropogenic load, with the exception of nitrate. However, a methodology based in PM2.5 measurement alone is not adequate for monitoring the impact of primary particulate emissions (such as ceramic emissions) on air quality, since the major ambient air particles derived from these emissions are mainly in the range of 2.5-10 μm. Consequently, in areas characterised by major secondary particulate emissions, PM2.5 monitoring should detect anthropogenic particulate pollutants without crustal particulate interference, whereas PM10 measurements should be used in areas with major primary anthropogenic particulate emissions.
Yu, Ben; Fu, Xuewu; Yin, Runsheng; Zhang, Hui; Wang, Xun; Lin, Che-Jen; Wu, Chuansheng; Zhang, Yiping; He, Nannan; Fu, Pingqing; Wang, Zifa; Shang, Lihai; Sommar, Jonas; Sonke, Jeroen E; Maurice, Laurence; Guinot, Benjamin; Feng, Xinbin
2016-09-06
The isotopic composition of atmospheric total gaseous mercury (TGM) and particle-bound mercury (PBM) and mercury (Hg) in litterfall samples have been determined at urban/industrialized and rural sites distributed over mainland China for identifying Hg sources and transformation processes. TGM and PBM near anthropogenic emission sources display negative δ(202)Hg and near-zero Δ(199)Hg in contrast to relatively positive δ(202)Hg and negative Δ(199)Hg observed in remote regions, suggesting that different sources and atmospheric processes force the mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) in the air samples. Both MDF and MIF occur during the uptake of atmospheric Hg by plants, resulting in negative δ(202)Hg and Δ(199)Hg observed in litter-bound Hg. The linear regression resulting from the scatter plot relating the δ(202)Hg to Δ(199)Hg data in the TGM samples indicates distinct anthropogenic or natural influences at the three study sites. A similar trend was also observed for Hg accumulated in broadleaved deciduous forest foliage grown in areas influenced by anthropogenic emissions. The relatively negative MIF in litter-bound Hg compared to TGM is likely a result of the photochemical reactions of Hg(2+) in foliage. This study demonstrates the diagnostic stable Hg isotopic composition characteristics for separating atmospheric Hg of different source origins in China and provides the isotopic fractionation clues for the study of Hg bioaccumulation.
Davis, Harley T.; Aelion, C. Marjorie; McDermott, Suzanne; Lawson, Andrew B.
2009-01-01
Determining sources of neurotoxic metals in rural and urban soils is important for mitigating human exposure. Surface soil from four areas with significant clusters of mental retardation and developmental delay (MR/DD) in children, and one control site were analyzed for nine metals and characterized by soil type, climate, ecological region, land use and industrial facilities using readily-available GIS-based data. Kriging, principal component analysis (PCA) and cluster analysis (CA) were used to identify commonalities of metal distribution. Three MR/DD areas (one rural and two urban) had similar soil types and significantly higher soil metal concentrations. PCA and CA results suggested that Ba, Be and Mn were consistently from natural sources; Pb and Hg from anthropogenic sources; and As, Cr, Cu, and Ni from both sources. Arsenic had low commonality estimates, was highly associated with a third PCA factor, and had a complex distribution, complicating mitigation strategies to minimize concentrations and exposures. PMID:19361902
Characterizing the anthropogenic signature in the LCLU dynamics in the Central Asia region
NASA Astrophysics Data System (ADS)
Tatarskii, V.; Sokolik, I. N.; de Beurs, K.; Shiklomanov, A. I.
2017-12-01
Humans have been changing the LCLU dynamics over time through the world. In the Central Asia region, these changes have been especially pronounced due to the political and economic transformation. We present a detailed analysis, focusing on identifying and quantifying the anthropogenic signature in the water and land use across the region. We have characterized the anthropogenic dust emission by combining the modeling and observations. The model is a fully coupled model called WRF-Chem-DuMo that takes explicitly into account the vegetation treatment in modeling the dust emission. We have reconstructed the anthropogenic dust sources in the region, such as the retreat of the Aral Sea, changes in agricultural fields, etc. In addition, we characterize the anthropogenic water use dynamics, including the changes in the water use for the agricultural production. Furthermore, we perform an analysis to identify the anthropogenic signature in the NDVI pattern. The NDVI were analyzed in conjunction with the meteorological fields that were simulated at the high special resolution using the WRF model. Meteorological fields of precipitation and temperature were used for the correlation analysis to separate the natural vs. anthropogenic changes. In this manner, we were able to identify the regions that have been affected by human activities. We will present the quantitative assessment of the anthropogenic changes. The diverse consequences for the economy of the region, as well as, the environment will be addressed.
Aquatic noise pollution: implications for individuals, populations, and ecosystems.
Kunc, Hansjoerg P; McLaughlin, Kirsty Elizabeth; Schmidt, Rouven
2016-08-17
Anthropogenically driven environmental changes affect our planet at an unprecedented scale and are considered to be a key threat to biodiversity. According to the World Health Organization, anthropogenic noise is one of the most hazardous forms of anthropogenically driven environmental change and is recognized as a major global pollutant. However, crucial advances in the rapidly emerging research on noise pollution focus exclusively on single aspects of noise pollution, e.g. on behaviour, physiology, terrestrial ecosystems, or on certain taxa. Given that more than two-thirds of our planet is covered with water, there is a pressing need to get a holistic understanding of the effects of anthropogenic noise in aquatic ecosystems. We found experimental evidence for negative effects of anthropogenic noise on an individual's development, physiology, and/or behaviour in both invertebrates and vertebrates. We also found that species differ in their response to noise, and highlight the potential underlying mechanisms for these differences. Finally, we point out challenges in the study of aquatic noise pollution and provide directions for future research, which will enhance our understanding of this globally present pollutant. © 2016 The Author(s).
Aquatic noise pollution: implications for individuals, populations, and ecosystems
Kunc, Hansjoerg P.; McLaughlin, Kirsty Elizabeth; Schmidt, Rouven
2016-01-01
Anthropogenically driven environmental changes affect our planet at an unprecedented scale and are considered to be a key threat to biodiversity. According to the World Health Organization, anthropogenic noise is one of the most hazardous forms of anthropogenically driven environmental change and is recognized as a major global pollutant. However, crucial advances in the rapidly emerging research on noise pollution focus exclusively on single aspects of noise pollution, e.g. on behaviour, physiology, terrestrial ecosystems, or on certain taxa. Given that more than two-thirds of our planet is covered with water, there is a pressing need to get a holistic understanding of the effects of anthropogenic noise in aquatic ecosystems. We found experimental evidence for negative effects of anthropogenic noise on an individual's development, physiology, and/or behaviour in both invertebrates and vertebrates. We also found that species differ in their response to noise, and highlight the potential underlying mechanisms for these differences. Finally, we point out challenges in the study of aquatic noise pollution and provide directions for future research, which will enhance our understanding of this globally present pollutant. PMID:27534952
NASA Astrophysics Data System (ADS)
Larson, T. E.; Perkins, G.; Longmire, P.; Heikoop, J. M.; Fessenden, J. E.; Rearick, M.; Fabyrka-Martin, J.; Chrystal, A. E.; Dale, M.; Simmons, A. M.
2009-12-01
The groundwater system beneath Los Alamos National Laboratory has been affected by multiple sources of anthropogenic nitrate contamination. Average NO3-N concentrations of up to 18.2±1.7 mg/L have been found in wells in the perched intermediate aquifer beneath one of the more affected sites within Mortandad Canyon. Sources of nitrate potentially reaching the alluvial and intermediate aquifers include: (1) sewage effluent, (2) neutralized nitric acid, (3) neutralized 15N-depleted nitric acid (treated waste from an experiment enriching nitric acid in 15N), and (4) natural background nitrate. Each of these sources is unique in δ18O and δ15N space. Using nitrate stable isotope ratios, a mixing model for the three anthropogenic sources of nitrate was established, after applying a linear subtraction of the background component. The spatial and temporal variability in nitrate contaminant sources through Mortandad Canyon is clearly shown in ternary plots. While microbial denitrification has been shown to change groundwater nitrate stable isotope ratios in other settings, the redox potential, relatively high dissolved oxygen content, increasing nitrate concentrations over time, and lack of observed NO2 in these wells suggest minimal changes to the stable isotope ratios have occurred. Temporal trends indicate that the earliest form of anthropogenic nitrate in this watershed was neutralized nitric acid. Alluvial wells preserve a trend of decreasing nitrate concentrations and mixing models show decreasing contributions of 15N-depleted nitric acid. Nearby intermediate wells show increasing nitrate concentrations and mixing models indicate a larger component derived from 15N-depleted nitric acid. These data indicate that the pulse of neutralized 15N-depleted nitric acid that was released into Mortandad Canyon between 1986 and 1989 has infiltrated through the alluvial aquifer and is currently affecting two intermediate wells. This hypothesis is consistent with previous research suggesting that the perched intermediate aquifers in the Mortandad Canyon watershed are recharged locally from the overlying alluvial aquifers.
Geomorphic and land cover identification of dust sources in the eastern Great Basin of Utah, U.S.A.
NASA Astrophysics Data System (ADS)
Hahnenberger, Maura; Nicoll, Kathleen
2014-01-01
This study identifies anthropogenically disturbed areas and barren playa surfaces as the two primary dust source types that repeatedly contribute to dust storm events in the eastern Great Basin of western Utah, U.S.A. This semi-arid desert region is an important contributor to dust production in North America, with this study being the first to specifically identify and characterize regional dust sources. From 2004 to 2010, a total of 51 dust event days (DEDs) affected the air quality in Salt Lake City, UT. MODIS satellite imagery during 16 of these DEDs was analyzed to identify dust plumes, and assess the characteristics of dust source areas. A total of 168 plumes were identified, and showed mobilization of dust from Quaternary deposits located within the Bonneville Basin. This analysis identifies 4 major and 5 secondary source areas for dust in this region, which produce dust primarily during the spring and fall months and during moderate or greater drought conditions, with a Palmer Drought Index (PDI) of - 2 or less. The largest number of observed dust plumes (~ 60% of all plumes) originated from playas (ephemeral lakes) and are classified as barren land cover with a silty clay soil sediment surface. Playa surfaces in this region undergo numerous recurrent anthropogenic disturbances, including military operations and anthropogenic water withdrawal. Anthropogenic disturbance is necessary to produce dust from the vegetated landscape in the eastern Great Basin, as evidenced by the new dust source active from 2008 to 2010 in the area burned by the 2007 Milford Flat Fire; this fire was the largest in Utah's history due to extensive cover of invasive cheatgrass (Bromus tectorum) along with drought conditions. However, dust mobilization from the Milford Flat Burned Area was limited to regions that had been significantly disturbed by post-fire land management techniques that consisted of seeding, followed by chaining or tilling of the soil. Dust storms in the eastern Great Basin negatively impact air quality and transportation in the populated regions of Utah; this study details an improved forecasting protocol for dust storm events that will benefit transportation planning and improve public health.
NASA Astrophysics Data System (ADS)
Catharine, D.; Strong, C.; Lin, J. C.; Cherkaev, E.; Mitchell, L.; Stephens, B. B.; Ehleringer, J. R.
2016-12-01
The rising level of atmospheric carbon dioxide (CO2), driven by anthropogenic emissions, is the leading cause of enhanced radiative forcing. Increasing societal interest in reducing anthropogenic greenhouse gas emissions call for a computationally efficient method of evaluating anthropogenic CO2 source emissions, particularly if future mitigation actions are to be developed. A multiple-box atmospheric transport model was constructed in conjunction with a pre-existing fossil fuel CO2 emission inventory to estimate near-surface CO2 mole fractions and the associated anthropogenic CO2 emissions in the Salt Lake Valley (SLV) of northern Utah, a metropolitan area with a population of 1 million. A 15-year multi-site dataset of observed CO2 mole fractions is used in conjunction with the multiple-box model to develop an efficient method to constrain anthropogenic emissions through inverse modeling. Preliminary results of the multiple-box model CO2 inversion indicate that the pre-existing anthropogenic emission inventory may over-estimate CO2 emissions in the SLV. In addition, inversion results displaying a complex spatial and temporal distribution of urban emissions, including the effects of residential development and vehicular traffic will be discussed.
Inferring ancient Agave cultivation practices from contemporary genetic patterns.
Parker, Kathleen C; Trapnell, Dorset W; Hamrick, J L; Hodgson, Wendy C; Parker, Albert J
2010-04-01
Several Agave species have played an important ethnobotanical role since prehistory in Mesoamerica and semiarid areas to the north, including central Arizona. We examined genetic variation in relict Agave parryi populations northeast of the Mogollon Rim in Arizona, remnants from anthropogenic manipulation over 600 years ago. We used both allozymes and microsatellites to compare genetic variability and structure in anthropogenically manipulated populations with putative wild populations, to assess whether they were actively cultivated or the result of inadvertent manipulation, and to determine probable source locations for anthropogenic populations. Wild populations were more genetically diverse than anthropogenic populations, with greater expected heterozygosity, polymorphic loci, effective number of alleles and allelic richness. Anthropogenic populations exhibited many traits indicative of past active cultivation: fixed heterozygosity for several loci in all populations (nonexistent in wild populations); fewer multilocus genotypes, which differed by fewer alleles; and greater differentiation among populations than was characteristic of wild populations. Furthermore, manipulated populations date from a period when changes in the cultural context may have favoured active cultivation near dwellings. Patterns of genetic similarity among populations suggest a complex anthropogenic history. Anthropogenic populations were not simply derived from the closest wild A. parryi stock; instead they evidently came from more distant, often more diverse, wild populations, perhaps obtained through trade networks in existence at the time of cultivation.
NASA Astrophysics Data System (ADS)
Wu, Rongrong; Bo, Yu; Li, Jing; Li, Lingyu; Li, Yaqi; Xie, Shaodong
2016-02-01
A method was developed to establish a comprehensive anthropogenic VOC emission inventory in China, in which a four-level source categorization was proposed, and an emission factor determination system together with a reference database were developed. And this was applied to establish VOC emission inventories for the period 2008-2012. Results show China's anthropogenic VOC emissions increased from 22.45 Tg in 2008 to 29.85 Tg in 2012 at an annual average rate of 7.38%, with Shandong, Guangdong, Jiangsu, Zhejiang and Hebei provinces being the largest emitters. Industrial processes, transportation and solvent utilization were the key sources, accounting for 39.3%, 25.6%, and 14.9% of the total emissions in 2012, respectively. Passenger cars, biofuel combustion, coke production, field burning of biomass, and raw chemical manufacturing were the primary VOC sources nationwide. The key sources for each province were different because of the disparate industry and energy structure. China's VOC emissions displayed remarkable spatial variation, with emissions in the east and southeast regions being much larger than in the northwest, and the high emission areas mainly centered in the Bohai Economic Rim, the Yangtze River Delta, the Pearl River Delta and the Sichuan Basin. The size of high emission areas expanded over the period 2008-2012, with heavily polluted city clusters gradually emerging.
Gao, Bo; Wei, Xin; Zhou, Huaidong; Lu, Jin; Hao, Hong; Wan, Xiaohong
2014-01-01
A geochemical study of Three Gorges Reservoir (TGR) sediments was carried out to analyze the concentrations, distribution, accumulation, and potential sources of the seldom monitored trace elements (SMTEs). The mean concentrations of Li, B, Be, Bi, V, Co, Ga, Sn, Sb, and Tl were 47.08, 2.47, 59.15, 0.50, 119.20, 17.83, 30.31, 3.25, 4.14, and 0.58 mg/kg, respectively. The concentrations of total SMTEs, together with their spatial distribution, showed that the SMTEs were mainly due to anthropogenic inputs in the region of TGR. The assessment by Geoaccumulation Index indicates that Tl, Be, V, Co, and Fe are at the unpolluted level; Bi, Li, Ga, and Sn were at the “uncontaminated to moderately contaminated” level. However, B was classified as “moderately contaminated” level and Sb was ranked as “strongly contaminated” level. The pollution level of the SMTEs is Sb > B > Bi > Li > Ga > Sn > Tl > Be > V > Co > Fe. The results of Correlation Analysis and Principal Component Analysis indicated Be, V, Co, Ga, Sn, Tl, Bi, and Fe in sediments have a natural source. B and Li were positively correlated with each other and mainly attributed into similar anthropogenic input. In addition, Sb has less relationship with other SMTEs, indicating that Sb has another kind of anthropogenic source. PMID:25136647
Ayuso, Robert A.; Foley, Nora K.
2018-01-01
Isotopic discrimination can be an effective tool in establishing a direct link between sources of Pb contamination and the presence of anomalously high concentrations of Pb in waters, soils, and organisms. Residential wells supplying water containing up to 1600 ppb Pb to houses built on the former Mohr orchards commercial site, near Allentown, Pennsylvania, United States, were evaluated to discern anthropogenic from geogenic sources. Pb and Sr isotopic data and REE data were determined for waters from residential wells, test wells (drilled for this study), and surface waters from pond and creeks. Local soils, sediments, bedrock, Zn-Pb mineralization and coal were also analyzed, together with locally used Pb-As pesticide. Pb isotope data for residential wells, test wells, and surface waters show substantial overlap with Pb data reflecting anthropogenic actions (e.g., burning fossil fuels, industrial and urban processing activities). Limited contributions of Pb from bedrock, soils, and pesticides are evident. High Pb concentrations in the residential waters are likely related to Pb in groundwater accumulating in sediment in the residential water tanks. The Pb isotope features of waters in underlying shallow aquifers that supply residential wells in the region are best interpreted as reflecting a legacy of anthropogenic Pb rather than geogenic Pb.
Legacy of human-induced C erosion and burial on soil-atmosphere C exchange.
Van Oost, Kristof; Verstraeten, Gert; Doetterl, Sebastian; Notebaert, Bastiaan; Wiaux, François; Broothaerts, Nils; Six, Johan
2012-11-20
Carbon exchange associated with accelerated erosion following land cover change is an important component of the global C cycle. In current assessments, however, this component is not accounted for. Here, we integrate the effects of accelerated C erosion across point, hillslope, and catchment scale for the 780-km(2) Dijle River catchment over the period 4000 B.C. to A.D. 2000 to demonstrate that accelerated erosion results in a net C sink. We found this long-term C sink to be equivalent to 43% of the eroded C and to have offset 39% (17-66%) of the C emissions due to anthropogenic land cover change since the advent of agriculture. Nevertheless, the erosion-induced C sink strength is limited by a significant loss of buried C in terrestrial depositional stores, which lagged the burial. The time lag between burial and subsequent loss at this study site implies that the C buried in eroded terrestrial deposits during the agricultural expansion of the last 150 y cannot be assumed to be inert to further destabilization, and indeed might become a significant C source. Our analysis exemplifies that accounting for the non-steady-state C dynamics in geomorphic active systems is pertinent to understanding both past and future anthropogenic global change.
Legacy of human-induced C erosion and burial on soil–atmosphere C exchange
Van Oost, Kristof; Verstraeten, Gert; Doetterl, Sebastian; Notebaert, Bastiaan; Wiaux, François; Broothaerts, Nils; Six, Johan
2012-01-01
Carbon exchange associated with accelerated erosion following land cover change is an important component of the global C cycle. In current assessments, however, this component is not accounted for. Here, we integrate the effects of accelerated C erosion across point, hillslope, and catchment scale for the 780-km2 Dijle River catchment over the period 4000 B.C. to A.D. 2000 to demonstrate that accelerated erosion results in a net C sink. We found this long-term C sink to be equivalent to 43% of the eroded C and to have offset 39% (17–66%) of the C emissions due to anthropogenic land cover change since the advent of agriculture. Nevertheless, the erosion-induced C sink strength is limited by a significant loss of buried C in terrestrial depositional stores, which lagged the burial. The time lag between burial and subsequent loss at this study site implies that the C buried in eroded terrestrial deposits during the agricultural expansion of the last 150 y cannot be assumed to be inert to further destabilization, and indeed might become a significant C source. Our analysis exemplifies that accounting for the non–steady-state C dynamics in geomorphic active systems is pertinent to understanding both past and future anthropogenic global change. PMID:23134723
NASA Astrophysics Data System (ADS)
Salvati, Agnese; Palme, Massimo; Inostroza, Luis
2017-10-01
Although Urban Heat Island (UHI) is a fundamental effect modifying the urban climate, being widely studied, the relative weight of the parameters involved in its generation is still not clear. This paper investigates the hierarchy of importance of eight parameters responsible for UHI intensity in the Mediterranean context. Sensitivity analyses have been carried out using the Urban Weather Generator model, considering the range of variability of: 1) city radius, 2) urban morphology, 3) tree coverage, 4) anthropogenic heat from vehicles, 5) building’s cooling set point, 6) heat released to canyon from HVAC systems, 7) wall construction properties and 8) albedo of vertical and horizontal surfaces. Results show a clear hierarchy of significance among the considered parameters; the urban morphology is the most important variable, causing a relative change up to 120% of the annual average UHI intensity in the Mediterranean context. The impact of anthropogenic sources of heat such as cooling systems and vehicles is also significant. These results suggest that urban morphology parameters can be used as descriptors of the climatic performance of different urban areas, easing the work of urban planners and designers in understanding a complex physical phenomenon, such as the UHI.
Sound the alarm: A meta-analysis on the effect of aquatic noise on fish behavior and physiology.
Cox, Kieran; Brennan, Lawrence P; Gerwing, Travis G; Dudas, Sarah E; Juanes, Francis
2018-07-01
The aquatic environment is increasingly bombarded by a wide variety of noise pollutants whose range and intensity are increasing with each passing decade. Yet, little is known about how aquatic noise affects marine communities. To determine the implications that changes to the soundscape may have on fishes, a meta-analysis was conducted focusing on the ramifications of noise on fish behavior and physiology. Our meta-analysis identified 42 studies that produced 2,354 data points, which in turn indicated that anthropogenic noise negatively affects fish behavior and physiology. The most predominate responses occurred within foraging ability, predation risk, and reproductive success. Additionally, anthropogenic noise was shown to increase the hearing thresholds and cortisol levels of numerous species while tones, biological, and environmental noise were most likely to affect complex movements and swimming abilities. These findings suggest that the majority of fish species are sensitive to changes in the aquatic soundscape, and depending on the noise source, species responses may have extreme and negative fitness consequences. As such, this global synthesis should serve as a warning of the potentially dire consequences facing marine ecosystems if alterations to aquatic soundscapes continue on their current trajectory. © 2018 John Wiley & Sons Ltd.
THE GENOTOXICITY OF AMBIENT OUTDOOR AIR, A REVIEW: SALMONELLA MUTAGENICITY
The genotoxicity of ambient outdoor air, a review: Salmonella mutagenicity
Abstract
Mutagens in urban air pollution come from anthropogenic sources (especially combustion sources) and are products of airborne chemical reactions. Bacterial mutation tests have been used ...
HETEROGENEOUS SOOT NANOSTRUCTURE IN ATMOSPHERIC AND COMBUSTION SOURCE AEROSOLS
Microscopic images of soot emissions from wildfire and a wide range of anthropogenic combustion sources show that the nanostructures of individual particles in these emissions are predominantly heterogeneous, decidedly influenced by the fuel composition and by the particular comb...
Barringer, J.L.; Reilly, P.A.; Eberl, D.D.; Blum, A.E.; Bonin, J.L.; Rosman, R.; Hirst, B.; Alebus, M.; Cenno, K.; Gorska, M.
2011-01-01
Glauconite-bearing deposits are found worldwide, but As levels have been determined for relatively few. The As content of glauconites in sediments of the Inner Coastal Plain of New Jersey can exceed 100mg/kg, and total As concentrations (up to 5.95??g/L) found historically and recently in streamwaters exceed the State standard. In a major watershed of the Inner Coastal Plain, chemical " fingerprints" were developed for streambed sediments and groundwater to identify contributions of As to the watershed from geologic and anthropogenic sources. The fingerprint for streambed sediments, which included Be, Cr, Fe and V, indicated that As was predominantly of geologic origin. High concentrations of dissolved organic C, nutrients (and Cl-) in shallow groundwater indicated anthropogenic inputs that provided an environment where microbial activity released As from minerals to groundwater discharging to the stream. Particulates in streamwater during high flow constituted most of the As load; the chemical patterns for these particulates resembled the geologic fingerprint of the streambed sediments. The As/Cr ratio of these suspended particles likely indicates they derived not only from runoff, but from groundwater inputs, because As contributed by groundwater is sequestered on streambed sediments. Agricultural inputs of As were not clearly identified, although chemical characteristics of some sediments indicated vehicle-related inputs of metals. Sediment sampling during dry and wet years showed that, under differing hydrologic conditions, local anthropogenic fingerprints could be obscured but the geologic fingerprint, indicating glauconitic sediments as an As source, was robust. ?? 2011.
NASA Astrophysics Data System (ADS)
Kyser, Kurt; Lahusen, Larry; Drever, Garth; Dunn, Colin; Leduc, Evelyne; Chipley, Don
2015-09-01
The response in elemental concentrations and Pb isotopes in various surface media from the Cigar West unconformity-type uranium deposit located at a depth of 450 m were measured to ascertain if element migration from the deposit can be detected at the surface. The media included clay-size fractions separated from the A2, B and C soil horizons, and tree cores and twigs from black spruce (Picea mariana) and jack pine (Pinus banksiana) trees. Lead isotopes were used to trace any effect on the surface media from the deposit at depth because the 207Pb/206Pb ratios in the ore are < 0.1, whereas the background values in the basin are > 0.7 and modern anthropogenic Pb from aerosols are near 0.9. The tree cores record their lowest and therefore most radiogenic 207Pb/206Pb ratios of < 0.7 near the surface projection of the deposit and associated structures, particularly in tree rings that predate any exploration and drilling activity in the area. The median 207Pb/206Pb ratios increase in the order C, B soil horizon clays, tree cores, A2 soil clays and twigs because of the increasing contribution of common Pb with high ratios from anthropogenic sources that affect the shallowest media the most. Although this anthropogenic Pb as well as that from the background dominates the composition of all media at the surface and the contribution from the deposit at depth is diminished toward the surface, ore-related Pb is still present as a few percent of the composition of pathfinder elements and Pb isotopes.
Global dust sources detection using MODIS Deep Blue Collection 6 aerosol products
NASA Astrophysics Data System (ADS)
Pérez García-Pando, C.; Ginoux, P. A.
2015-12-01
Our understanding of the global dust cycle is limited by a dearth of information about dust sources, especially small-scale features which could account for a large fraction of global emissions. Remote sensing sensors are the most useful tool to locate dust sources. These sensors include microwaves, visible channels, and lidar. On the global scale, major dust source regions have been identified using polar orbiting satellite instruments. The MODIS Deep Blue algorithm has been particularly useful to detect small-scale sources such as floodplains, alluvial fans, rivers, and wadis , as well as to identify anthropogenic sources from agriculture. The recent release of Collection 6 MODIS aerosol products allows to extend dust source detection to the entire land surfaces, which is quite useful to identify mid to high latitude dust sources and detect not only dust from agriculture but fugitive dust from transport and industrial activities. This presentation will overview the advantages and drawbacks of using MODIS Deep Blue for dust detection, compare to other instruments (polar orbiting and geostationary). The results of Collection 6 with a new dust screening will be compared against AERONET. Applications to long range transport of anthropogenic dust will be presented.
Hyperspectral observation of anthropogenic and biogenic pollution in coastal zone
NASA Astrophysics Data System (ADS)
Lavrova, Olga; Loupian, Evgeny; Mityagina, Marina; Uvarov, Ivan
The work presents results of anthropogenic and biogenic pollution detection in coastal zones of the Black and Caspian Seas based on satellite hyperspetral data provided by the Hyperion and HICO instruments. Techniques developed on the basis of the analysis of spectral characteristics calculated in special points were employed to address the following problems: (a) assessment of the blooming intensity of cyanobacteria and their distribution in bays of western Crimea and discrimination between anthropogenic pollutant discharge events and algae bloom; (b) detection of anthropogenic pollution in Crimean lakes utilized as industrial liquid discharge reservoirs; (c) detection of oil pollution in areas of shelf oil production in the Caspian Sea. Information values of different spectral bands and their composites were estimated in connection with the retrieval of the main sea water components: phytoplankton, suspended matter and colored organic matter, and also various anthropogenic pollutants, including oil. Software tools for thematic hyperspectral data processing in application to the investigation of sea coastal zones and internal water bodies were developed on the basis of the See the Sea geoportal created by the Space Research Institute RAS. The geoportal is focused on the study of processes in the world ocean with the emphasis on the advantages of satellite systems of observation. The tools that were introduced into the portal allow joint analysis of quasi-simultaneous satellite data, in particular data from the Hyperion, HICO, OLI Landsat-8, ETM Landsat-7 and TM Landsat-5 instruments. Results of analysis attempts combining data from different sensors are discussed. Their strong and weak points are highlighted. The study was completed with partial financial support from The Russian Foundation for Basic Research grants # 14-05-00520-a and 13-07-12017.
Derryberry, Elizabeth P; Danner, Raymond M; Danner, Julie E; Derryberry, Graham E; Phillips, Jennifer N; Lipshutz, Sara E; Gentry, Katherine; Luther, David A
2016-01-01
Soundscapes pose both evolutionarily recent and long-standing sources of selection on acoustic communication. We currently know more about the impact of evolutionarily recent human-generated noise on communication than we do about how natural sounds such as pounding surf have shaped communication signals over evolutionary time. Based on signal detection theory, we hypothesized that acoustic phenotypes will vary with both anthropogenic and natural background noise levels and that similar mechanisms of cultural evolution and/or behavioral flexibility may underlie this variation. We studied song characteristics of white-crowned sparrows (Zonotrichia leucophrys nuttalli) across a noise gradient that includes both anthropogenic and natural sources of noise in San Francisco and Marin counties, California, USA. Both anthropogenic and natural soundscapes contain high amplitude low frequency noise (traffic or surf, respectively), so we predicted that birds would produce songs with higher minimum frequencies in areas with higher amplitude background noise to avoid auditory masking. We also anticipated that song minimum frequencies would be higher than the projected lower frequency limit of hearing based on site-specific masking profiles. Background noise was a strong predictor of song minimum frequency, both within a local noise gradient of three urban sites with the same song dialect and cultural evolutionary history, and across the regional noise gradient, which encompasses 11 urban and rural sites, several dialects, and several anthropogenic and natural sources of noise. Among rural sites alone, background noise tended to predict song minimum frequency, indicating that urban sites were not solely responsible for driving the regional pattern. These findings support the hypothesis that songs vary with local and regional soundscapes regardless of the source of noise. Song minimum frequency from five core study sites was also higher than the lower frequency limit of hearing at each site, further supporting the hypothesis that songs vary to transmit through noise in local soundscapes. Minimum frequencies leveled off at noisier sites, suggesting that minimum frequencies are constrained to an upper limit, possibly to retain the information content of wider bandwidths. We found evidence that site noise was a better predictor of song minimum frequency than territory noise in both anthropogenic and natural soundscapes, suggesting that cultural evolution rather than immediate behavioral flexibility is responsible for local song variation. Taken together, these results indicate that soundscapes shape song phenotype across both evolutionarily recent and long-standing soundscapes.
Derryberry, Graham E.; Phillips, Jennifer N.; Lipshutz, Sara E.; Gentry, Katherine; Luther, David A.
2016-01-01
Soundscapes pose both evolutionarily recent and long-standing sources of selection on acoustic communication. We currently know more about the impact of evolutionarily recent human-generated noise on communication than we do about how natural sounds such as pounding surf have shaped communication signals over evolutionary time. Based on signal detection theory, we hypothesized that acoustic phenotypes will vary with both anthropogenic and natural background noise levels and that similar mechanisms of cultural evolution and/or behavioral flexibility may underlie this variation. We studied song characteristics of white-crowned sparrows (Zonotrichia leucophrys nuttalli) across a noise gradient that includes both anthropogenic and natural sources of noise in San Francisco and Marin counties, California, USA. Both anthropogenic and natural soundscapes contain high amplitude low frequency noise (traffic or surf, respectively), so we predicted that birds would produce songs with higher minimum frequencies in areas with higher amplitude background noise to avoid auditory masking. We also anticipated that song minimum frequencies would be higher than the projected lower frequency limit of hearing based on site-specific masking profiles. Background noise was a strong predictor of song minimum frequency, both within a local noise gradient of three urban sites with the same song dialect and cultural evolutionary history, and across the regional noise gradient, which encompasses 11 urban and rural sites, several dialects, and several anthropogenic and natural sources of noise. Among rural sites alone, background noise tended to predict song minimum frequency, indicating that urban sites were not solely responsible for driving the regional pattern. These findings support the hypothesis that songs vary with local and regional soundscapes regardless of the source of noise. Song minimum frequency from five core study sites was also higher than the lower frequency limit of hearing at each site, further supporting the hypothesis that songs vary to transmit through noise in local soundscapes. Minimum frequencies leveled off at noisier sites, suggesting that minimum frequencies are constrained to an upper limit, possibly to retain the information content of wider bandwidths. We found evidence that site noise was a better predictor of song minimum frequency than territory noise in both anthropogenic and natural soundscapes, suggesting that cultural evolution rather than immediate behavioral flexibility is responsible for local song variation. Taken together, these results indicate that soundscapes shape song phenotype across both evolutionarily recent and long-standing soundscapes. PMID:27128443
NASA Astrophysics Data System (ADS)
Jacobson, Yitzhak; Yam, Ruth; Shemesh, Aldo
2017-04-01
The Mediterranean Sea is a region under high anthropogenic stress, thus a hotspot for climate change studies. Natural conditions, such as SST, productivity, precipitation and dust fluxes along with human induced activity affect seawater chemistry. We study millennial variability of trace elements in East Mediterranean Sea high-resolution records, in attempt to connect them to environmental factors. The Mediterranean reef builder Vermetid, D. petraeum is a sessile gastropod, secreting its aragonite shells in tidal zones. Cores of Vermetid reefs from the South Eastern Mediterranean (Israel) were previously analyzed by Sisma?Ventura et al. (2014) to reconstruct seawater surface temperature (SST) and δ13C of dissolved inorganic carbon (DIC). In this study we analyzed trace elements of these vermetid cores, and reconstructed millennial records of elements to calcium (el/Ca) molar ratios. Vermetid trace element contents from recent decades are mostly in agreement with known values for marine biogenic aragonites from corals and mollusk. We divide vermetid trace element records into three element groups: 1) Sr and U are related to SST and DIC. These elements correlate with major climatic events of the last millennium, such as the Medieval Warm Period (900-1300 AD) and the Little Ice Age (1450-1850 AD). 2) Pb and Cd are related to anthropogenic pollution and demonstrate industrial sourced trends throughout the anthropocene (since 1750 AD). 3) Terrogenous elements, including Fe, Al, Mn and V. Al in seawater and sediments has been used to trace water masses and land derived sediment source. We observe a major change in average vermetid Al/Fe ratios from 0.5 to 2.5 over the recorded period (n=72). This vermetid Al/Fe change points at a possible shift from Nilotic sediments (0.1-0.5 Al/Fe molar ratio) to Saharan dust ratio (2-4 Al/Fe molar ratio). Mn and V show a similar variability to Fe. Understanding the variability of vermetid TE can help us interpret the relative dominance of different climate systems and anthropogenic processes on the East Mediterranean environment.
Organic Geochemistry of the Tohoku Tsunami Deposits of 2011 (Japan)
NASA Astrophysics Data System (ADS)
Reicherter, K. R.; Schwarzbauer, J.; Szczucinski, W.; Jaffe, B. E.
2014-12-01
Geochemical investigations on paleotsunami deposits have mainly focused on inorganic proxies. Organic geochemistry has been used to distinguish between terrestrial and marine matter within the sediments, reflecting the mixture and transport of marine and terrestrial matter. The approach using organic substances with indicative properties (anthropogenic and xenobiotic compounds) for recent tsunami deposits is novel, but the approach of using specific bio- and anthropogenic markers indicators to determine (pre)historic and recent processes and impacts already exists. The Tohoku-oki tsunami in March 2011 showed the huge threat that tsunamis pose to society and landscape, including flooding of coastal lowlands and erosion/deposition of sediments. The mainly sandy tsunamites reach more than 4.5 km inland as there were run-up heights of ca. 10 m in the Sendai plain near the Sendai airport. The destruction of infrastructure by wave action and flooding was accompanied by the release of environmental pollutants (e.g. fuels, fats, tarmac, plastics, heavy metals, etc.) contaminating the coastal areas and ocean over large areas. To detect and characterize this process, we analyzed several sedimentary archives from the Bay of Sendai area (by using the same sample material as Szczucinski et al., 2012 from rice paddies of the Sendai Plain, Japan). The layers representing the tsunami deposits have been compared with pre-tsunami samples (supposedly to be unaffected) by means of organic-geochemical analyses based on GC/MS. Natural compounds and their diagenetic transformation products have been tested as marker compounds and proxies. The relative composition of fatty acids, n-alkanes, sesquiterpenes and further substances pointed to significant variations before and after the tsunami event. Additionally, anthropogenic marker compounds (such as soil derived pesticides, source specific PAHs, halogenated aromatics from industrial sources) have been detected and quantified. Concentration profiles of distinct terrestrial pollutants revealed shifts either to increasing but for selected compounds also to decreasing contamination levels. We will extend and test the approach in future on paleotsunami deposits of the 869 AD Jogan event and others. Szczucinski et al. 2012, Sed. Geol., 282:40-56.
Poor health is associated with use of anthropogenic resources in an urban carnivore
Murray, Maureen; Edwards, Mark A.; Abercrombie, Bill; St. Clair, Colleen Cassady
2015-01-01
Rates of encounters between humans and wildlife are increasing in cities around the world, especially when wildlife overlap with people in time, space and resources. Coyotes (Canis latrans) can make use of anthropogenic resources and reported rates of conflict have increased in cities across North America. This increase may be linked to individual differences in the use of human food and developed areas. We compared the relationships between coyote age, sex or health and the use of anthropogenic resources, which we defined as using developed areas over large home ranges, being active during the day, and consuming anthropogenic food. To do so, we applied GPS collars to 19 coyotes and sampled hair for stable isotope analysis. Eleven coyotes appeared to be healthy and eight were visibly infested with sarcoptic mange (Sarcoptes scabiei), a mite that causes hair loss. Diseased coyotes used more developed areas, had larger monthly home ranges, were more active during the day, and assimilated less protein than coyotes that appeared to be healthy. We speculate that anthropogenic food provides a low-quality but easily accessible food source for diseased coyotes, which in turn may increase reliance on it and other anthropogenic resources to promote encounters with people. PMID:25876843
NASA Astrophysics Data System (ADS)
Vasileiou, Eleni; Perraki, Maria; Stamatis, George; Gartzos, Efthimios
2014-05-01
High concentrations of heavy metals, particularly of the toxic hexavalent chromium, are recorded in surface and ground waters in many areas, and constitute one of the most severe environmental problems nowadays. The natural genesis of chromium is associated with the geological environment (peridotites and serpentintites). Chromium is structured in many minerals, mainly in spinel (e.g. chromite), in silicate minerals such as phyllosilicate serpentine minerals, chlorite, talc and chain-silicate minerals of pyroxene and amphibole group. Chromium is found in two forms in soils, waters and rocks, the hexavalent and the trivalent one. The relation between Cr(III) and Cr(VI) strongly depends on pH and oxidative properties of the area; however, in most cases, Cr(III) is the dominating variant. The natural oxidation of trivalent to hexavalent chromium can be achieved by manganese oxides, H2O2, O2 gas and oxy-hydroxides of trivalent iron. Anthropogenic factors may also cause the process of chromium's oxidation. In the Psachna basin, Central Euboea, Greece, high concentrations of hexavalent chromium were recently measured in spring- and drill- waters. In this work, we study the effect of the geological environment and of the anthropogenic activities on the water quality with emphasis on chromium. A detailed geochemical, petrological and mineralogical study of rocks and soils was carried out by means of optical microscopy, XRF, XRD and SEM/EDS. Ground and surface water samples were physically characterized and hydrochemically studied by means of ICP and AAF. Combined result evaluation indicates a natural source for the trivalent chromium in waters, attributed to the alteration of Cr-bearing minerals of the ultramafic rocks. However the oxidation of trivalent to hexavalent chromium results from anthropogenic activities, mainly from intensive agricultural activities and the extensive use of fertilizers and pesticides causing nitrate pollution in groundwater. It has been shown that there is a strong correlation between the nitrate concentration and the hexavalent chromium one; therefore it is believed that the presence of nitrates operates as oxidant for trivalent to hexavalent chromium. On the contrary, in natural areas, without anthropogenic activities, it was observed that the hexavalent chromium concentration in groundwater is lower. Besides, a strong correlation was also observed between chromium and yttrium concentrations in natural areas, pointing to a natural source of chromium, since chromium and yttrium exist naturally in a strongly bonded form.
Evaluating and ranking the vulnerability of global marine ecosystems to anthropogenic threats.
Halpern, Benjamin S; Selkoe, Kimberly A; Micheli, Fiorenza; Kappel, Carrie V
2007-10-01
Marine ecosystems are threatened by a suite of anthropogenic stressors. Mitigating multiple threats is a daunting task, particularly when funding constraints limit the number of threats that can be addressed. Threats are typically assessed and prioritized via expert opinion workshops that often leave no record of the rationale for decisions, making it difficult to update recommendations with new information. We devised a transparent, repeatable, and modifiable method for collecting expert opinion that describes and documents how threats affect marine ecosystems. Experts were asked to assess the functional impact, scale, and frequency of a threat to an ecosystem; the resistance and recovery time of an ecosystem to a threat; and the certainty of these estimates. To quantify impacts of 38 distinct anthropogenic threats on 23 marine ecosystems, we surveyed 135 experts from 19 different countries. Survey results showed that all ecosystems are threatened by at least nine threats and that nine ecosystems are threatened by >90% of existing threats. The greatest threats (highest impact scores) were increasing sea temperature, demersal destructive fishing, and point-source organic pollution. Rocky reef, coral reef, hard-shelf, mangrove, and offshore epipelagic ecosystems were identified as the most threatened. These general results, however, may be partly influenced by the specific expertise and geography of respondents, and should be interpreted with caution. This approach to threat analysis can identify the greatest threats (globally or locally), most widespread threats, most (or least) sensitive ecosystems, most (or least) threatened ecosystems, and other metrics of conservation value. Additionally, it can be easily modified, updated as new data become available, and scaled to local or regional settings, which would facilitate informed and transparent conservation priority setting.
2013-01-01
Background Anthropogenic activities introduce materials increasing levels of many dangerous substances for the environmental quality and being hazardous to human health. Major attention has been given to those elements able to alter the environment and endanger human health. The airborne particulate matter pollutant is considered one of the most difficult task in environmental chemistry for its complex composition and implications complicating notably the behavior comprehension. So, for investigating deeply the elemental composition we used two nuclear techniques, Neutron Activation Analysis and Photon Activation Analysis, characterized by high sensitivity, precision and accuracy. An important task has been devoted to the investigation of Quality Control (QC) and Quality Assurance (QA) of the methodology used in this study. This study was therefore extended as far back as possible in time (from 1965 until 2000) in order to analyze the trend of airborne concentration of pollutant elements in connection with the industrial and lifestyle growth during the entire period. Results Almost all the elements may be attributed to long-range transport phenomena from other natural and/or anthropogenic sources: this behavior is common to all the periods studied even if a very light decreasing trend can be evidenced from 1970 to 2002. Finally, in order to investigate a retrospective study of elements in PM10 and their evolution in relationship with the natural or anthropogenic origins, we have investigated the Enrichment Factors. The study shows the EF trends for some elements in PM10 during four decades. Conclusions The two nuclear techniques have allowed to reach elevated sensibility/accuracy levels for determining elements at very low concentrations (trace and ultra-trace levels). The element concentrations determined in this study do not basically show a significant level of attention from a toxicological point of view. PMID:24196275
Towards mechanistic representations of SOA from BVOC + NO3 reactions
Monoterpene reaction with nitrate radicals is a significant source of organic aerosol in the southeast United States. This source of organic aerosol represents an anthropogenic control on biogenic organic aerosol since nitrate radicals result from NOx emissions and are generally ...
THE ASSOCIATION OF LAND USE/LAND COVER AND NUTRIENT LEVELS IN MARYLAND STREAMS
Anthropogenic nonpoint sources of nutrients are known to cause accelerated eutrophication of estuaries. The Chesapeake Bay is one of the world's largest estuaries exhibiting the eutrophication problem caused by pollution from various land use activities. The sources contributing ...
WATER QUALITY EARLY WARNING SYSTEMS FOR SOURCE WATER PROTECTION
Source waters of the U.S. are vulnerable to natural and anthropogenic factors affecting quality for use as both a drinking water and ecological media. Important factors include physical parameters such as increased turbidity, ecological cycles such as algal blooms, and episodic ...
APPLICATION OF PROTEOMIC METHODS TO ARSENIC EXPOSURE RESEARCH
Arsenic, an environmental contaminant, is introduced to drinking water through the leaching of soil and the result of anthropogenic sources such as industrial effluents and combustion of fossil fuels. It also occurs naturally in ground water sources in some geographic areas. Chro...
Organic compounds in aerosols from selected European sites - Biogenic versus anthropogenic sources
NASA Astrophysics Data System (ADS)
Alves, Célia; Vicente, Ana; Pio, Casimiro; Kiss, Gyula; Hoffer, Andras; Decesari, Stefano; Prevôt, André S. H.; Minguillón, María Cruz; Querol, Xavier; Hillamo, Risto; Spindler, Gerald; Swietlicki, Erik
2012-11-01
Atmospheric aerosol samples from a boreal forest (Hyytiälä, April 2007), a rural site in Hungary (K-puszta, summer 2008), a polluted rural area in Italy (San Pietro Capofiume, Po Valley, April 2008), a moderately polluted rural site in Germany located on a meadow (Melpitz, May 2008), a natural park in Spain (Montseny, March 2009) and two urban background locations (Zurich, December 2008, and Barcelona, February/March 2009) were collected. Aliphatics, polycyclic aromatic hydrocarbons, carbonyls, sterols, n-alkanols, acids, phenolic compounds and anhydrosugars in aerosols were chemically characterised by gas chromatography-mass spectrometry, along with source attribution based on the carbon preference index (CPI), the ratios between the unresolved and the chromatographically resolved aliphatics, the contribution of wax n-alkanes, n-alkanols and n-alkanoic acids from plants, diagnostic ratios of individual target compounds and source-specific markers to organic carbon ratios. In spite of transboundary pollution episodes, Hyytiälä registered the lowest levels among all locations. CPI values close to 1 for the aliphatic fraction of the Montseny aerosol suggest that the anthropogenic input may be associated with the transport of aged air masses from the surrounding industrial/urban areas, which superimpose the locally originated hydrocarbons with biogenic origin. Aliphatic and aromatic hydrocarbons in samples from San Pietro Capofiume reveal that fossil fuel combustion is a major source influencing the diel pattern of concentrations. This source contributed to 25-45% of the ambient organic carbon (OC) at the Po Valley site. Aerosols from the German meadow presented variable contributions from both biogenic and anthropogenic sources. The highest levels of vegetation wax components and biogenic secondary organic aerosol (SOA) products were observed at K-puszta, while anthropogenic SOA compounds predominated in Barcelona. The primary vehicular emissions in the Spanish city accounted for around 25-30% of the OC in aerosols. Besides the traffic input (10% of OC), residential wood burning was found to be another dominant emission source contributing to the atmospheric aerosol (up to 38% of OC) at the Swiss urban location. It was estimated that around 10% of the OC mass in the urban sites originates from cooking emissions. Aerosols from the urban area of Zurich presented a much higher PAH content, and benzo(a)pyrene equivalent concentrations sometimes exceeding the mandatory limit.
Continuing global monitoring of anthropogenic and volcanic SO2 sources from Aura/OMI to SNPP/OMPS
NASA Astrophysics Data System (ADS)
Li, C.; Krotkov, N. A.; Carn, S. A.; Joiner, J.; McLinden, C. A.; Fioletov, V.
2017-12-01
Sulfur dioxide (SO2) is an important trace gas that has significant impacts on air quality, the climate, and stratospheric ozone. It is predominantly emitted from anthropogenic sources such as coal-fired power plants and smelters, but also has sizable sources from volcanic activity. The Ozone Monitoring Instrument (OMI) aboard NASA's Earth Observing System (EOS) Aura spacecraft has been providing global observations of both anthropogenic and volcanic SO2 since its launch in 2004. The Ozone Mapping and Profiler Suite (OMPS) nadir mapper, launched aboard the NASA/NOAA Suomi National Polar-orbiting Partnership (SNPP) satellite in 2011, will continue the 13+ year OMI SO2 time series. However, it is a significant challenge to build a coherent data record between OMI and OMPS, as the SO2 signal is relatively weak and its retrieval is subject to a number of interferences such as ozone absorption. Additionally, the two instruments also have different spectral and spatial resolutions that result in different sensitivities to SO2. Even a relatively small error in retrievals, due to either algorithmic or instrumental factors, may lead to a large inter-instrument bias in SO2. In this presentation, we report on our latest effort and progress in developing EOS continuity SNPP/OMPS SO2 products. We have applied a consistent retrieval technique based on principal component analysis (PCA) of measured radiance data to both OMI and OMPS. We show that the PCA retrieval technique, which extracts principal components (PCs) from measured radiances and applies these PCs in spectral fitting to minimize the effects of various interfering processes, is capable of producing highly consistent OMI and OMPS SO2 data for both anthropogenic sources and large volcanic eruptions. To gain a quantitative understanding of the two instruments' capabilities of monitoring SO2 sources, we have also applied a new emission estimation technique that combines satellite SO2 and wind information to both of them. This method allows SO2 emissions from 500 sources worldwide to be detected and quantified from OMI data. The OMPS-based emission estimates using the same method agree well with OMI-based ones, although OMPS detects fewer of the smaller sources seen by OMI, owing to its coarser spatial resolution.
Recommended metric for tracking visibility progress in the Regional Haze Rule.
Gantt, Brett; Beaver, Melinda; Timin, Brian; Lorang, Phil
2018-05-01
For many national parks and wilderness areas with special air quality protections (Class I areas) in the western United States (U.S.), wildfire smoke and dust events can have a large impact on visibility. The U.S. Environmental Protection Agency's (EPA) 1999 Regional Haze Rule used the 20% haziest days to track visibility changes over time even if they are dominated by smoke or dust. Visibility on the 20% haziest days has remained constant or degraded over the last 16 yr at some Class I areas despite widespread emission reductions from anthropogenic sources. To better track visibility changes specifically associated with anthropogenic pollution sources rather than natural sources, the EPA has revised the Regional Haze Rule to track visibility on the 20% most anthropogenically impaired (hereafter, most impaired) days rather than the haziest days. To support the implementation of this revised requirement, the EPA has proposed (but not finalized) a recommended metric for characterizing the anthropogenic and natural portions of the daily extinction budget at each site. This metric selects the 20% most impaired days based on these portions using a "delta deciview" approach to quantify the deciview scale impact of anthropogenic light extinction. Using this metric, sulfate and nitrate make up the majority of the anthropogenic extinction in 2015 on these days, with natural extinction largely made up of organic carbon mass in the eastern U.S. and a combination of organic carbon mass, dust components, and sea salt in the western U.S. For sites in the western U.S., the seasonality of days selected as the 20% most impaired is different than the seasonality of the 20% haziest days, with many more winter and spring days selected. Applying this new metric to the 2000-2015 period across sites representing Class I areas results in substantial changes in the calculated visibility trend for the northern Rockies and southwest U.S., but little change for the eastern U.S. Changing the approach for tracking visibility in the Regional Haze Rule allows the EPA, states, and the public to track visibility on days when reductions in anthropogenic emissions have the greatest potential to improve the view. The calculations involved with the recommended metric can be incorporated into the routine IMPROVE (Interagency Monitoring of Protected Visual Environments) data processing, enabling rapid analysis of current and future visibility trends. Natural visibility conditions are important in the calculations for the recommended metric, necessitating the need for additional analysis and potential refinement of their values.
Anthropogenic contamination of tap water, beer, and sea salt
2018-01-01
Plastic pollution has been well documented in natural environments, including the open waters and sediments within lakes and rivers, the open ocean and even the air, but less attention has been paid to synthetic polymers in human consumables. Since multiple toxicity studies indicate risks to human health when plastic particles are ingested, more needs to be known about the presence and abundance of anthropogenic particles in human foods and beverages. This study investigates the presence of anthropogenic particles in 159 samples of globally sourced tap water, 12 brands of Laurentian Great Lakes beer, and 12 brands of commercial sea salt. Of the tap water samples analyzed, 81% were found to contain anthropogenic particles. The majority of these particles were fibers (98.3%) between 0.1–5 mm in length. The range was 0 to 61 particles/L, with an overall mean of 5.45 particles/L. Anthropogenic debris was found in each brand of beer and salt. Of the extracted particles, over 99% were fibers. After adjusting for particles found in lab blanks for both salt and beer, the average number of particles found in beer was 4.05 particles/L with a range of 0 to 14.3 particles/L and the average number of particles found in each brand of salt was 212 particles/kg with a range of 46.7 to 806 particles/kg. Based on consumer guidelines, our results indicate the average person ingests over 5,800 particles of synthetic debris from these three sources annually, with the largest contribution coming from tap water (88%). PMID:29641556
NASA Astrophysics Data System (ADS)
Liu, J.; Li, X.; Mauzerall, D. L.; Emmons, L. K.; Horowitz, L. W.; Guo, Y.; Tao, S.
2015-12-01
Due to a lack of industrialization in Western China, surface air there was, until recently, believed to be relatively unpolluted. However, recent measurements and modeling studies have found high levels of ozone (O3) there. Based on the state-of-the-science global chemical transport model MOZART-4, we identify the origin, pathway, and mechanism of trans-Eurasian transport of air pollutants to Western China in 2000. MOZART-4 generally simulates well the observed surface O3 over inland areas of China. Simulations find surface ozone concentrations over Western China on average to be about 10 ppbv higher than Eastern China. Using sensitivity studies as well as a fully-tagged approach, we find that anthropogenic emissions from all Eurasian regions except China contribute 10-15 ppbv surface O3 over Western China, superimposed upon a 35-40 ppbv natural background. Transport from European anthropogenic sources to Northwestern China results in 2-6 ppbv O3 enhancements in spring and summer. Indian anthropogenic sources strongly influence O3 over the Tibetan Plateau during the summer monsoon. Transport of O3 originating from emissions in the Middle East occasionally reach Western China and increase surface ozone there by about 1-4 ppbv. These influences are of similar magnitude as trans-Pacific and transatlantic transport of O3 and its precursors, indicating the significance of trans-Eurasian ozone transport in hemispheric transport of air pollution. Our study further indicates that mitigation of anthropogenic emissions from Europe, the Indian subcontinent, and the Middle East could benefit public health and agricultural productivity in Western China.
A stress ecology framework for comprehensive risk assessment of diffuse pollution.
van Straalen, Nico M; van Gestel, Cornelis A M
2008-12-01
Environmental pollution is traditionally classified as either localized or diffuse. Local pollution comes from a point source that emits a well-defined cocktail of chemicals, distributed in the environment in the form of a gradient around the source. Diffuse pollution comes from many sources, small and large, that cause an erratic distribution of chemicals, interacting with those from other sources into a complex mixture of low to moderate concentrations over a large area. There is no good method for ecological risk assessment of such types of pollution. We argue that effects of diffuse contamination in the field must be analysed in the wider framework of stress ecology. A multivariate approach can be applied to filter effects of contaminants from the many interacting factors at the ecosystem level. Four case studies are discussed (1) functional and structural properties of terrestrial model ecosystems, (2) physiological profiles of microbial communities, (3) detritivores in reedfield litter, and (4) benthic invertebrates in canal sediment. In each of these cases the data were analysed by multivariate statistics and associations between ecological variables and the levels of contamination were established. We argue that the stress ecology framework is an appropriate assessment instrument for discriminating effects of pollution from other anthropogenic disturbances and naturally varying factors.
NASA Astrophysics Data System (ADS)
Agudelo-Vera, Claudia M.; Blokker, Mirjam; de Kater, Henk; Lafort, Rob
2017-09-01
The water temperature in the drinking water distribution system and at customers' taps approaches the surrounding soil temperature at a depth of 1 m. Water temperature is an important determinant of water quality. In the Netherlands drinking water is distributed without additional residual disinfectant and the temperature of drinking water at customers' taps is not allowed to exceed 25 °C. In recent decades, the urban (sub)surface has been getting more occupied by various types of infrastructures, and some of these can be heat sources. Only recently have the anthropogenic sources and their influence on the underground been studied on coarse spatial scales. Little is known about the urban shallow underground heat profile on small spatial scales, of the order of 10 m × 10 m. Routine water quality samples at the tap in urban areas have shown up locations - so-called hotspots - in the city, with relatively high soil temperatures - up to 7 °C warmer - compared to the soil temperatures in the surrounding rural areas. Yet the sources and the locations of these hotspots have not been identified. It is expected that with climate change during a warm summer the soil temperature in the hotspots can be above 25 °C. The objective of this paper is to find a method to identify heat sources and urban characteristics that locally influence the soil temperature. The proposed method combines mapping of urban anthropogenic heat sources, retrospective modelling of the soil temperature, analysis of water temperature measurements at the tap, and extensive soil temperature measurements. This approach provided insight into the typical range of the variation of the urban soil temperature, and it is a first step to identifying areas with potential underground heat stress towards thermal underground management in cities.
Harkness, Jennifer S; Darrah, Thomas H; Moore, Myles T; Whyte, Colin J; Mathewson, Paul D; Cook, Tyson; Vengosh, Avner
2017-11-07
Molybdenum (Mo) is an essential trace nutrient but has negative health effects at high concentrations. Groundwater typically has low Mo (<2 μg/L), and elevated levels are associated with anthropogenic contamination, although geogenic sources have also been reported. Coal combustion residues (CCRs) are enriched in Mo, and thus present a potential anthropogenic contamination source. Here, we use diagnostic geochemical tracers combined with groundwater residence time indicators to investigate the sources of Mo in drinking-water wells from shallow aquifers in a region of widespread CCR disposal in southeastern Wisconsin. Samples from drinking-water wells were collected in areas near and away from known CCR disposal sites, and analyzed for Mo and inorganic geochemistry indicators, including boron and strontium isotope ratios, along with groundwater tritium-helium and radiogenic 4 He in-growth age-dating techniques. Mo concentrations ranged from <1 to 149 μg/L. Concentrations exceeding the U.S. Environmental Protection Agency health advisory of 40 μg/L were found in deeper, older groundwater (mean residence time >300 y). The B (δ 11 B = 22.9 ± 3.5‰) and Sr ( 87 Sr/ 86 Sr = 0.70923 ± 0.00024) isotope ratios were not consistent with the expected isotope fingerprints of CCRs, but rather mimic the compositions of local lithologies. The isotope signatures combined with mean groundwater residence times of more than 300 years for groundwater with high Mo concentrations support a geogenic source of Mo to the groundwater, rather than CCR-induced contamination. This study demonstrates the utility of a multi-isotope approach to distinguish between fossil fuel-related and natural sources of groundwater contamination.
Liu, Liang-Ying; Wei, Gao-Ling; Wang, Ji-Zhong; Guan, Yu-Feng; Wong, Charles S; Wu, Feng-Chang; Zeng, Eddy Y
2013-10-15
Sediment has been recognized as a gigantic sink of organic materials and therefore can record temporal input trends. To examine the impact of anthropogenic activities on the marginal seas off China, sediment cores were collected from the Yellow Sea, the inner shelf of the East China Sea (ECS), and the South China Sea (SCS) to investigate the sources and spatial and temporal variations of organic materials, i.e., total organic carbon (TOC) and aliphatic hydrocarbons. The concentration ranges of TOC were 0.5-1.29, 0.63-0.83, and 0.33-0.85%, while those of Σn-C14-35 (sum of n-alkanes with carbon numbers of 14-35) were 0.08-1.5, 0.13-1.97, and 0.35-0.96 μg/g dry weight in sediment cores from the Yellow Sea, ECS inner shelf, and the SCS, respectively. Terrestrial higher plants were an important source of aliphatic hydrocarbons in marine sediments off China. The spatial distribution of Σn-C14-35 concentrations and source diagnostic ratios suggested a greater load of terrestrial organic materials in the Yellow Sea than in the ECS and SCS. Temporally, TOC and Σn-C14-35 concentrations increased with time and peaked at either the surface or immediate subsurface layers. This increase was probably reflective of elevated inputs of organic materials to marginal seas off China in recent years, and attributed partly to the impacts of intensified anthropogenic activities in mainland China. Source diagnostics also suggested that aliphatic hydrocarbons were mainly derived from biogenic sources, with a minority in surface sediment layers from petroleum sources, consistent with the above-mentioned postulation.
Understanding the Impacts of Anthropogenic Sound on Beaked Whales
2006-01-01
Arbelo, M. 2005. ‘Gas and fat embolic syndrome’ involving a mass stranding of beaked whales (family Ziphiidae) exposed to anthropogenic sonar signals. Vet...intracranial and acoustic fat injuries in the strandings and mortalities was not clear. Analysis of acoustic sources used in the Bahamas naval exercises revealed...Macroscopic examination revealed that the whales had severe, diffuse congestion and haemorrhages, especially in the fat in the jaw, around the ears, in the
Zohar, I; Bookman, R; Levin, N; de Stigter, H; Teutsch, N
2014-12-02
Pollution history of Pb and other trace metals was reconstructed for the first time for the Eastern Mediterranean, from a small urban winter pond (Dora, Netanya), located at the densely populated coastal plain of Israel. An integrated approach including geochemical, sedimentological, and historical analyses was employed to study sediments from the center of the pond. Profiles of metal concentrations (Pb, Zn, V, Ni, Cu, Cr, Co, Cd, and Hg) and Pb isotopic composition denote two main eras of pre- and post-19th century. The deeper sediment is characterized by low concentrations and relatively constant 206Pb/207Pb (around 1.20), similar to natural Pb sources, with slight indications of ancient anthropogenic activity. The upper sediment displays an upward increase in trace metal concentrations, with the highest enrichment factor for Pb (18.4). Lead fluxes and isotopic composition point to national/regional petrol-Pb emissions as the major contributor to Pb contamination, overwhelming other potential local and transboundary sources. Traffic-related metals are correlated with Pb, emphasizing the polluting inputs of traffic. The Hg profile, however, implies global pollution rather than local sources.
NASA Astrophysics Data System (ADS)
Hegerl, G. C.; Polson, D.; Bollasina, M. A.; Ming, Y.
2015-12-01
Anthropogenic aerosols are a key driver 4 of historical changes in Summer monsoon precipition in the Northern Hemisphere. Detection and attribution studies have shown that the reduction in Northern Hemisphere precipitation over the second half of the 20th century is driven by anthropogenic aerosol emissions. Here we apply these same methods to investigate changes in the West African and South Asian monsoons and identify the source regions of the anthropogenic aerosols that drive the observed changes. Historical climate model simulations are used to derive fingerprints of aerosol forcing for different regions of the globe. Comparing model changes with observations show that the changes in West African monsoon preciptiation are driven by remote aerosol emissions from North America and Europe, while changes in South Asian monsoon precipitation are driven by local aerosol emissions.
Marijić, Vlatka Filipović; Perić, Mirela Sertić; Kepčija, Renata Matoničkin; Dragun, Zrinka; Kovarik, Ivana; Gulin, Vesna; Erk, Marijana
2016-01-01
The present study was undertaken to obtain a better understanding of the seasonal variability of total dissolved metal/metalloid levels and physicochemical parameters within small- to medium-size freshwater ecosystems in temperate climate region. The research was conducted in four seasons in the Sutla River, medium-size polluted, and the Črnomerec Stream, small-size unpolluted watercourse in Croatia. In the Sutla River, characterized by the rural/industrial catchment, physicochemical parameters and total dissolved metal concentrations of 21 trace and 4 macro elements were analysed downstream of the point source of pollution, the glass production facility, indicating for the first time their variability across four seasons. Based on dissolved oxygen, total dissolved solids, nutrient concentrations, conductivity and total chemical oxygen demand, quality status of the Sutla River was good, but moderate to poor during summer, what was additionally confirmed by the highest levels of the most of 25 measured metals/metalloids in summer. Comparison with the reference small-size watercourse, the Črnomerec Stream, indicated significant anthropogenic impact on the Sutla River, most evident for Fe, Mn, Mo, Ni, Pb, Rb and Tl levels (3-70-fold higher in the Sutla River across all seasons). Generally, presented results indicated significant decrease of the water quality in the anthropogenically impacted small- to medium-size watercourses in summer, regarding physicochemical water parameters and total dissolved metal/metalloid concentrations, and pointed to significant seasonality of these parameters. Confirmed seasonality of river ecological status indicates that seasonal assessment represents a prerequisite for proper classification of the water quality in small- to medium-size temperate rivers.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Buonanno, G., E-mail: buonanno@unicas.i; Stabile, L.; Avino, P.
2010-07-15
In the last years numerous epidemiological studies were carried out to evaluate the effects of particulate matter on human health. In industrialized areas, anthropogenic activities highly contribute to the fine and ultrafine particle concentrations. Then, it is important to characterize the evolution of particle size distribution and chemical composition near these emission points. Waste incineration represents a favorable technique for reducing the waste volume. However, in the past, municipal waste incinerators (MWIs) had a bad reputation due to the emission of toxic combustion byproducts. Consequently, the risk perception of the people living near MWIs is very high even if inmore » Western countries waste incineration has nowadays to be considered a relatively clean process from a technical point of view. The study here presented has an exemplary meaning for developing appropriate management and control strategies for air quality in the surrounding of MWIs and to perform exposure assessment for populations involved. Environment particles were continuously measured through a SMPS/APS system over 12 months. The monitoring site represents a downwind receptor of a typical MWI. Furthermore, elements and organic fractions were measured by means of the Instrumental Neutron Activation Analysis and using dichotomous and high volume samplers. Annual mean values of 8.6 x 10{sup 3} +- 3.7 x 10{sup 2} part. cm{sup -3} and 31.1 +- 9.0 mug m{sup -3} were found for number and mass concentration, typical of a rural site. Most of the elements can be attributed to long-range transport from other natural and/or anthropogenic sources. Finally, the Polycyclic Aromatic Hydrocarbons present low concentrations with a mean value of 24.6 ng m{sup -3}.« less
Lignin geochemistry of sediments from the Narragansett Bay Estuary
NASA Astrophysics Data System (ADS)
Requejo, A. G.; Brown, John S.; Boehm, Paul D.
1986-12-01
Cupric oxide oxidation has been employed to characterize the lignin geochemistry of Narragansett Bay sediments. Lignin concentrations throughout the estuary are low when expressed on a carbon-normalized basis, but can be characterized as enriched when expressed on a mass-normalized basis. This implies substantial dilution of the sedimentary lignin by inputs of lignin-poor carbon. Lignin concentrations do not correlate with the 13C isotopic composition of the sedimentary organic matter. These results are consistent with a sediment lignin component consisting of varying amounts of vascular plant debris and lignin-depleted organic matter, the latter originating from both marine (planktonic) and terrestrial (uncharacterized) sources. Compositional plots of lignin-derived phenols show that sediments in the upper estuary are influenced to a greater extent by gymnosperm lignin sources than those in the mid-and lower estuary. Given the extent to which the upper estuary is affected by pollution sources, inputs from anthropogenic discharges are the most likely cause of these compositional differences. However, an evaluation of processed paper products as an "anthropogenic" lignin source indicates that the lignin content of these materials is insufficient to account for the levels found in the sediments. Subsurface lignin compositions at an upper estuary site reveal that lignin originating from the inferred anthropogenic sources disappears at a depth shallower than that which would be expected based on the distribution of other trace organic pollutants (hydrocarbons and several synthetic organic compounds). We speculate that differences in either the depositional history or the degree of preservation of these two compound classes are responsible for the observed trends.
NASA Astrophysics Data System (ADS)
Otvos, Ervin G.; Carter, Gregory A.
2013-09-01
Basic differences between non-deltaic regressive and deltaic transgressive barrier islands reflect major contrasts in geological settings and sediment sources. Two island groups on the N. Gulf of Mexico provide unique perspectives of genetic and geomorphic contrasts applicable in a worldwide context. The near-extinction of the deltaic transgressive Chandeleur barriers and reduction of the sturdier prograded Mississippi-Alabama (MS-AL) chain are related to differences in sediment sources, storm, and anthropogenic impact. 160 years of documentary evidence points to contrasting geological settings, development history, sediment sources, and island morphology as responsible for different island erodibility and life spans. The non-deltaic chain received larger volumes of coarser, less erodible medium sand from the NE Gulf coast. Onshore sand flux from reworked delta deposits received from the retreating delta shoreface initiated the fragile, thin, and isolated transgressive Chandeleur islands. Fine-grained sand from unconsolidated muds of abandoned Mississippi-St. Bernard delta lobes maintained two distinct transgressive barrier island categories. In the absence of quantitative data on cross-shore transport, discrepancies between estimated littoral drift volumes and sand reserves for nourishment remain unexplained. Medium-sandy MS-AL barriers have resisted storm events far better than delta barriers. However, even the former chain did undergo 26 to 53% area reduction since 1848. Anthropogenic intervention stymied island growth. Emerging intertidal berm-basins formed on sandy shoal platforms in storm-eliminated sectors have contributed to partial island recovery. Delta attrition by wave erosion, tectonic, and compactional subsidence had accelerated delta lobe and barrier island decay. Intensive storm erosion culminating in and following Hurricane Katrina came close to eradicate the highly vulnerable Chandeleur barrier chain. Lacking adequate nourishment, after devastating cyclones only small islands reemerge and persist temporarily from the shoal belt. A four-stage barrier evolution model, globally applicable to transgressive deltaic barriers, is based on documented changes in late Holocene Mississippi sub-deltas.
Cheng, Qingli; Wang, Ruiling; Huang, Wenhai; Wang, Wenlin; Li, Xudong
2015-06-01
The Yellow River Wetland National Nature Reserve (the Sanmenxia section) is an important area of the Yellow River for two important hydrologic gauging stations: the Sanmenxia reservoir and the Xiaolangdi reservoir. Seven sites along the section were selected: Jiziling, Dinghuwan, Houdi, Canglonghu, Shangcun, Wangguan, and Nancun. After the microwave digestion with aqua regia, concentrations of Cu, Pb, Cd, Cr, Zn, and Mn in the sediments were analyzed by flame atomic absorption spectrometry with air-acetylene flame. The results showed that all the concentrations of Cr detected were from the lithogenic source, and 63 % Mn, 48 % Pb, 41 % Cu, 20 % Cd, and 12 % Zn were from the anthropogenic source. The values of the index of geo-accumulation pointed out that there was moderate contamination of Mn at the Dinghuwan (1.04) and Houdi (1.00) sites (class 2), while the modified degree of contamination denoted that the contamination at the Houdi site (2.02) was moderate, nil to very low at the Nancun and Shangcun sites and low at the other sites, consisting with the tendency of pollution load index. For metal toxicity, the sediment pollution index indicated that the sediments of the Canglonghu site were low polluted, that of the Houdi site is nearly slightly contaminated, and those of others were natural and uncontaminated. It was vital to evaluate the degree of contamination with individual and overall elements and even with the metal toxicity. Cu, Pb, and Mn contaminations were aggravated in the Sanmenxia section, and there maybe was one of the main anthropogenic sources of these metals along the Yellow River. The findings were expected to update the current status of the heavy metal pollution in the Sanmenxia section as well as to create awareness concerning the sound condition of the whole reaches of the Yellow River.
Massive land system changes impact water quality of the Jhelum River in Kashmir Himalaya.
Rather, Mohmmad Irshad; Rashid, Irfan; Shahi, Nuzhat; Murtaza, Khalid Omar; Hassan, Khalida; Yousuf, Abdul Rehman; Romshoo, Shakil Ahmad; Shah, Irfan Yousuf
2016-03-01
The pristine aquatic ecosystems in the Himalayas are facing an ever increasing threat from various anthropogenic pressures which necessitate better understanding of the spatial and temporal variability of pollutants, their sources, and possible remedies. This study demonstrates the multi-disciplinary approach utilizing the multivariate statistical techniques, data from remote sensing, lab, and field-based observations for assessing the impact of massive land system changes on water quality of the river Jhelum. Land system changes over a period of 38 years have been quantified using multi-spectral satellite data to delineate the extent of different anthropogenically driven land use types that are the main non-point sources of pollution. Fifteen water quality parameters, at 12 sampling sites distributed uniformly along the length of the Jhelum, have been assessed to identify the possible sources of pollution. Our analysis indicated that 18% of the forested area has degraded into sparse forest or scrublands from 1972 to 2010, and the areas under croplands have decreased by 24% as people shifted from irrigation-intensive agriculture to orchard farming while as settlements showed a 397% increase during the observation period. One-way ANOVA revealed that all the water quality parameters had significant spatio-temporal differences (p < 0.01). Cluster analysis (CA) helped us to classify all the sampling sites into three groups. Factor analysis revealed that 91.84% of the total variance was mainly explained by five factors. Drastic changes in water quality of the Jhelum since the past three decades are manifested by increases in nitrate-nitrogen, TDS, and electric conductivity. The especially high levels of nitrogen (858 ± 405 μgL(-1)) and phosphorus (273 ± 18 μgL(-1)) in the Jhelum could be attributed to the reckless application of fertilizers, pesticides, and unplanned urbanization in the area.
Smucker, Nathan J; Kuhn, Anne; Cruz-Quinones, Carlos J; Serbst, Jonathan R; Lake, James L
2018-01-07
Watershed development and anthropogenic sources of nitrogen are among leading causes of negative impacts to aquatic ecosystems around the world. The δ 15 N of aquatic biota can be used as indicators of anthropogenic sources of nitrogen enriched in 15 N, but this mostly has been done at small spatial extents or to document effects of point sources. In this study, we sampled 77 sites along a forest to urban land cover gradient to examine food webs and the use of δ 15 N of periphyton and macroinvertebrate functional feeding groups (FFGs) as indicators of watershed development and nitrogen effects on streams. Functional feeding groups had low δ 15 N variability among taxa within sites. Mean absolute differences between individual taxa and their respective site FFG means were < 0.55‰, whereas site means of δ 15 N of FFGs had ranges of approximately 7-12‰ among sites. The δ 15 N of periphyton and macroinvertebrate FFGs distinguished least disturbed streams from those with greater watershed urbanization, and they were strongly correlated with increasing nitrogen concentrations and watershed impervious cover. Nonmetric multidimensional scaling, using δ 15 N of taxa, showed that changes in macroinvertebrate assemblages as a whole were associated with forest-to-urban and increasing nitrogen gradients. Assuming an average +3.4‰ per trophic level increase, δ 15 N of biota indicated that detrital pathways likely were important to food web structure, even in streams with highly developed watersheds. We used periphyton and macroinvertebrate FFG δ 15 N to identify possible management goals that can inform decisions affecting nutrients and watershed land use. Overall, the δ 15 N of periphyton and macroinvertebrates were strong indicators of watershed urban development effects on stream ecosystems, and thus, also could make them useful for quantifying the effectiveness of nitrogen, stream, and watershed management efforts.
Influences of climate and land use on contemporary ...
Human beings have greatly accelerated nitrogen and phosphorus flows from land to aquatic ecosystems, often resulting in eutrophication, harmful algal blooms, and hypoxia in lakes and coastal waters. Although differences in nitrogen export from watersheds have been clearly linked to a combination of human nitrogen sources and climate in the U.S., relatively less is known about how natural and anthropogenic landscape characteristics mediate losses of phosphorus from watersheds. We quantified major phosphorus inputs (fertilizer, manure, and human waste) and outputs (riverine export, crop harvest and sewage treatment) for 94 watersheds in 2012 across the continental U.S. and examined how climate, hydrology, soil characteristics, and land use influenced phosphorus exports from watersheds to rivers as total phosphorus and dissolved inorganic phosphorus concentrations and yields. We identified regional differences in major input sources as well as the importance of landscape mediating factors, highlighting the importance of both the biophysical and anthropogenic contexts on the relationship between major phosphorus sources and water quality. This study represents the most up-to-date spatially explicit inventory of anthropogenic P inputs and outputs for the conterminous United States. Linking this inventory with losses of phosphorus to waterways is an important step in understanding what policies and practices may be most effective in mitigating water quality problems.
Mercury in tropical and subtropical coastal environments
Costa, Monica F.; Landing, William M.; Kehrig, Helena A.; Barletta, Mário; Holmes, Christopher D.; Barrocas, Paulo R. G.; Evers, David C.; Buck, David G.; Vasconcellos, Ana Claudia; Hacon, Sandra S.; Moreira, Josino C.; Malm, Olaf
2012-01-01
Anthropogenic activities influence the biogeochemical cycles of mercury, both qualitatively and quantitatively, on a global scale from sources to sinks. Anthropogenic processes that alter the temporal and spatial patterns of sources and cycling processes are changing the impacts of mercury contamination on aquatic biota and humans. Human exposure to mercury is dominated by the consumption of fish and products from aquaculture operations. The risk to society and to ecosystems from mercury contamination is growing, and it is important to monitor these expanding risks. However, the extent and manner to which anthropogenic activities will alter mercury sources and biogeochemical cycling in tropical and sub-tropical coastal environments is poorly understood. Factors as (1) lack of reliable local/regional data; (2) rapidly changing environmental conditions; (3) governmental priorities and; (4) technical actions from supra-national institutions, are some of the obstacles to overcome in mercury cycling research and policy formulation. In the tropics and sub-tropics, research on mercury in the environment is moving from an exploratory “inventory” phase towards more process-oriented studies. Addressing biodiversity conservation and human health issues related to mercury contamination of river basins and tropical coastal environments are an integral part of paragraph 221 paragraph of the United Nations document “The Future We Want” issued in Rio de Janeiro in June 2012. PMID:22901765
The report discusses the development of emission factors for CO2, CO, CH4, NOx, and N2O for about 80 globally significant combustion sources in seven source categories: utility, industrial, fuel production, transportation, residential, commercial, and kilns/ovens/dryers. ecause o...
NASA Astrophysics Data System (ADS)
Michoud, Vincent; Sciare, Jean; Sauvage, Stéphane; Dusanter, Sébastien; Léonardis, Thierry; Gros, Valérie; Kalogridis, Cerise; Zannoni, Nora; Féron, Anaïs; Petit, Jean-Eudes; Crenn, Vincent; Baisnée, Dominique; Sarda-Estève, Roland; Bonnaire, Nicolas; Marchand, Nicolas; Langley DeWitt, H.; Pey, Jorge; Colomb, Aurélie; Gheusi, François; Szidat, Sonke; Stavroulas, Iasonas; Borbon, Agnès; Locoge, Nadine
2017-07-01
The ChArMEx (Chemistry and Aerosols Mediterranean Experiments) SOP2 (special observation period 2) field campaign took place from 15 July to 5 August 2013 in the western Mediterranean Basin at Ersa, a remote site in Cape Corse. During the campaign more than 80 volatile organic compounds (VOCs), including oxygenated species, were measured by different online and offline techniques. At the same time, an exhaustive description of the chemical composition of fine aerosols was performed with an aerosol chemical speciation monitor (ACSM). Low levels of anthropogenic VOCs (typically tens to hundreds of parts per trillion for individual species) and black carbon (0.1-0.9 µg m-3) were observed, while significant levels of biogenic species (peaking at the ppb level) were measured. Furthermore, secondary oxygenated VOCs (OVOCs) largely dominated the VOC speciation during the campaign, while organic matter (OM) dominated the aerosol chemical composition, representing 55 % of the total mass of non-refractory PM1 on average (average of 3.74 ± 1.80 µg m-3), followed by sulfate (27 %, 1.83 ± 1.06 µg m-3), ammonium (13 %, 0.90 ± 0.55 µg m-3) and nitrate (5 %, 0.31 ± 0.18 µg m-3). Positive matrix factorization (PMF) and concentration field (CF) analyses were performed on a database containing 42 VOCs (or grouped VOCs), including OVOCs, to identify the covariation factors of compounds that are representative of primary emissions or chemical transformation processes. A six-factor solution was found for the PMF analysis, including a primary and secondary biogenic factor correlated with temperature and exhibiting a clear diurnal profile. In addition, three anthropogenic factors characterized by compounds with various lifetimes and/or sources have been identified (long-lived, medium-lived and short-lived anthropogenic factors). The anthropogenic nature of these factors was confirmed by the CF analysis, which identified potential source areas known for intense anthropogenic emissions (north of Italy and southeast of France). Finally, a factor characterized by OVOCs of both biogenic and anthropogenic origin was found. This factor was well correlated with submicron organic aerosol (OA) measured by an aerosol chemical speciation monitor (ACSM), highlighting the close link between OVOCs and organic aerosols; the latter is mainly associated (96 %) with the secondary OA fraction. The source apportionment of OA measured by ACSM led to a three-factor solution identified as hydrogen-like OA (HOA), semi-volatile oxygenated OA (SV-OOA) and low volatility OOA (LV-OOA) for averaged mass concentrations of 0.13, 1.59 and 1.92 µg m-3, respectively. A combined analysis of gaseous PMF factors with inorganic and organic fractions of aerosols helped distinguish between anthropogenic continental and biogenic influences on the aerosol- and gas-phase compositions.
The major natural sources of airborne hydrogen fluoride (HF) are volcanic activity, ocean spray, and crustal weathering of fluoride-containing rocks. Anthropogenic sources include emissions from industrial operations such as aluminum and fluorocarbon production, and uranium proce...
Perfluoroalkyl substances (PFAS), such as perfluorooctane sulfonate (PFOS) and perfluorooctanoic acid (PFOA) , are persistent, globally distributed, anthropogenic compounds. The primary source(s) for human exposure are not well understood although within home exposure is likely i...
Sources of Mercury Exposure for U.S. Seafood Consumers: Implications for Policy
Recent policies attempting to reduce adverse effects of methylmercury exposure from fish consumption in the U.S. have targeted reductions in anthropogenic emissions from U.S. sources. Methods: We use models that simulate global atmospheric chemistry (GEOS-Chem); the fate, transp...
“A significant source of isoprene aerosol controlled by acidity”
“A significant source of isoprene aerosol controlled by acidity” by Pye et al.Abstract: Isoprene is a significant contributor to organic aerosol in the southeastern United States where biogenic hydrocarbons mix with anthropogenic emissions. In this work, CMAQ provides explicit p...
Lee, Yeonjung; Hur, Jin; Shin, Kyung-Hoon
2014-07-15
The characteristics and sources of organic matter in water of the Lake Shihwa, which receives inputs from rural, urban, and industrial areas, were evaluated by examining the biodegradable organic carbon concentration, fluorescence spectra, and carbon and nitrogen isotope ratios, especially during rainy season and dry season. The organic matter transported from rural areas was of refractory nature, while that of industrial origin decomposed rapidly. As compared to the dry season, the organic matter in the rainy season was characterized by a reduced labile fraction. During the dry season, the autochthonous organic matter dominated in the lake, however, the contributions of allochthonous organic sources by industrial and rural areas significantly increased at rainy season. This investigation revealed that the transport of organic matter of anthropogenic origin to the Lake Shihwa was mainly influenced by heavy rainfall. Moreover, each anthropogenic source could differently influence the occurrence of organic matter in water of the Lake Shihwa. Copyright © 2014 Elsevier Ltd. All rights reserved.
Michel, Anna P M; Kapit, Jason; Witinski, Mark F; Blanchard, Romain
2017-04-10
Methane is a powerful greenhouse gas that has both natural and anthropogenic sources. The ability to measure methane using an integrated path length approach such as an open/long-path length sensor would be beneficial in several environments for examining anthropogenic and natural sources, including tundra landscapes, rivers, lakes, landfills, estuaries, fracking sites, pipelines, and agricultural sites. Here a broadband monolithic distributed feedback-quantum cascade laser array was utilized as the source for an open-path methane sensor. Two telescopes were utilized for the launch (laser source) and receiver (detector) in a bistatic configuration for methane sensing across a 50 m path length. Direct-absorption spectroscopy was utilized with intrapulse tuning. Ambient methane levels were detectable, and an instrument precision of 70 ppb with 100 s averaging and 90 ppb with 10 s averaging was achieved. The sensor system was designed to work "off the grid" and utilizes batteries that are rechargeable with solar panels and wind turbines.
Airborne methane remote measurements reveal heavy-tail flux distribution in Four Corners region
Thorpe, Andrew K.; Thompson, David R.; Hulley, Glynn; Kort, Eric Adam; Vance, Nick; Borchardt, Jakob; Krings, Thomas; Gerilowski, Konstantin; Sweeney, Colm; Conley, Stephen; Bue, Brian D.; Aubrey, Andrew D.; Hook, Simon; Green, Robert O.
2016-01-01
Methane (CH4) impacts climate as the second strongest anthropogenic greenhouse gas and air quality by influencing tropospheric ozone levels. Space-based observations have identified the Four Corners region in the Southwest United States as an area of large CH4 enhancements. We conducted an airborne campaign in Four Corners during April 2015 with the next-generation Airborne Visible/Infrared Imaging Spectrometer (near-infrared) and Hyperspectral Thermal Emission Spectrometer (thermal infrared) imaging spectrometers to better understand the source of methane by measuring methane plumes at 1- to 3-m spatial resolution. Our analysis detected more than 250 individual methane plumes from fossil fuel harvesting, processing, and distributing infrastructures, spanning an emission range from the detection limit ∼ 2 kg/h to 5 kg/h through ∼ 5,000 kg/h. Observed sources include gas processing facilities, storage tanks, pipeline leaks, and well pads, as well as a coal mine venting shaft. Overall, plume enhancements and inferred fluxes follow a lognormal distribution, with the top 10% emitters contributing 49 to 66% to the inferred total point source flux of 0.23 Tg/y to 0.39 Tg/y. With the observed confirmation of a lognormal emission distribution, this airborne observing strategy and its ability to locate previously unknown point sources in real time provides an efficient and effective method to identify and mitigate major emissions contributors over a wide geographic area. With improved instrumentation, this capability scales to spaceborne applications [Thompson DR, et al. (2016) Geophys Res Lett 43(12):6571–6578]. Further illustration of this potential is demonstrated with two detected, confirmed, and repaired pipeline leaks during the campaign. PMID:27528660
Arctic Ocean sea ice drift origin derived from artificial radionuclides.
Cámara-Mor, P; Masqué, P; Garcia-Orellana, J; Cochran, J K; Mas, J L; Chamizo, E; Hanfland, C
2010-07-15
Since the 1950s, nuclear weapon testing and releases from the nuclear industry have introduced anthropogenic radionuclides into the sea, and in many instances their ultimate fate are the bottom sediments. The Arctic Ocean is one of the most polluted in this respect, because, in addition to global fallout, it is impacted by regional fallout from nuclear weapon testing, and indirectly by releases from nuclear reprocessing facilities and nuclear accidents. Sea-ice formed in the shallow continental shelves incorporate sediments with variable concentrations of anthropogenic radionuclides that are transported through the Arctic Ocean and are finally released in the melting areas. In this work, we present the results of anthropogenic radionuclide analyses of sea-ice sediments (SIS) collected on five cruises from different Arctic regions and combine them with a database including prior measurements of these radionuclides in SIS. The distribution of (137)Cs and (239,240)Pu activities and the (240)Pu/(239)Pu atom ratio in SIS showed geographical differences, in agreement with the two main sea ice drift patterns derived from the mean field of sea-ice motion, the Transpolar Drift and Beaufort Gyre, with the Fram Strait as the main ablation area. A direct comparison of data measured in SIS samples against those reported for the potential source regions permits identification of the regions from which sea ice incorporates sediments. The (240)Pu/(239)Pu atom ratio in SIS may be used to discern the origin of sea ice from the Kara-Laptev Sea and the Alaskan shelf. However, if the (240)Pu/(239)Pu atom ratio is similar to global fallout, it does not provide a unique diagnostic indicator of the source area, and in such cases, the source of SIS can be constrained with a combination of the (137)Cs and (239,240)Pu activities. Therefore, these anthropogenic radionuclides can be used in many instances to determine the geographical source area of sea-ice. Copyright 2010 Elsevier B.V. All rights reserved.
Low, Adrian; Ng, Charmaine; He, Jianzhong
2016-12-01
Urban watersheds from point sources are potential reservoirs of antibiotic resistance genes (ARGs). However, few studies have investigated urban watersheds of non-point sources. To understand the type of ARGs and bacteria that might carry such genes, we investigated two non-point source urban watersheds with different land-use profiles. Antibiotic resistance levels of two watersheds (R1, R3) were examined using heterotrophic plate counts (HPC) as a culturing method to obtain counts of bacteria resistant to seven antibiotics belonging to different classes (erythromycin, kanamycin, lincomycin, norfloxacin, sulfanilamide, tetracycline and trimethoprim). From the HPC study, 239 antibiotic resistant bacteria were characterized for resistance to more antibiotics. Furthermore, ARGs and antimicrobial biosynthesis genes were identified using GeoChip version 5.0 to elucidate the resistomes of surface waters in watersheds R1 and R3. The HPC study showed that water samples from R1 had significantly higher counts of bacteria resistant to erythromycin, kanamycin, norfloxacin, sulfanilamide, tetracycline and trimethoprim than those from R3 (Analysis of Similarity (ANOSIM), R = 0.557, p < 0.01). Of the seven antibiotics tested, lincomycin and trimethoprim resistant bacteria are greater in abundances. The 239 antibiotic resistant isolates represent a subset of resistant bacterial populations, including bacteria not previously known for resistance. Majority of the isolates had resistance to ampicillin, vancomycin, lincomycin and trimethoprim. GeoChip revealed similar ARGs in both watersheds, but with significantly higher intensities for tetX and β-lactamase B genes in R1 than R3. The genes with the highest average normalized intensities in R1 and R3 were tetracycline (tet) and fosfomycin (fosA) resistance genes, respectively. The higher abundance of tetX genes in R1 is congruent with the higher abundance of tetracycline resistant HPC observed in R1 samples. Strong correlations (r ≥ 0.8) of efflux pumps with antimicrobial biosynthesis genes suggest that natural production of antimicrobials may act as a selective pressure of transporter proteins in the absence of antibiotics from anthropogenic sources. In conclusion, distinct antibiotic resistant bacteria phylotypes and a variety of ARGs were present in the non-point sources urban watersheds of different land-use profiles, suggesting that ARG risk assessments and monitoring studies need to include these types of watersheds. Copyright © 2016 Elsevier Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Alier, M.; van Drooge, B. L.; Dall'Osto, M.; Querol, X.; Grimalt, J. O.; Tauler, R.
2013-10-01
This study investigates the contribution of potential sources to the submicron (PM1) organic aerosol (OA) simultaneously detected at an urban background (UB) and a road site (RS) in Barcelona during the 30 days of the intensive field campaign of SAPUSS (Solving Aerosol Problems by Using Synergistic Strategies, September-October 2010). A total of 103 filters at 12 h sampling time resolution were collected at both sites. Thirty-six neutral and polar organic compounds of known emission sources and photo-chemical transformation processes were analyzed by gas chromatography-mass spectrometry (GC-MS). The concentrations of the trace chemical compounds analyzed are herein presented and discussed. Additionally, OA source apportionment was performed by multivariate curve resolution-alternating least squares (MCR-ALS) and six OA components were identified at both sites: two were of primary anthropogenic OA origin and three of secondary OA origin, while a sixth one was not clearly defined. Primary organics from emissions of local anthropogenic activities (urban primary organic aerosol, or POA Urban), mainly traffic emissions but also cigarette smoke, contributed 43% (1.5 μg OC m-3) and 18% (0.4 μg OC m-3) to OA at RS and UB, respectively. A secondary primary source - biomass burning (BBOA) - was found in all the samples (average values 7% RS; 12% UB; 0.3 μg OC m-3), but this component was substantially contributing to OA only when the sampling sites were under influence of regional air mass circulation (REG.). Three secondary organic aerosol (SOA) components (describing overall 60% of the variance) were observed in the urban ambient PM1. Products of isoprene oxidation (SOA ISO) - i.e. 2-methylglyceric acid, C5 alkene triols and 2-methyltetrols - showed the highest abundance at both sites when the city was under influence of inland air masses. The overall concentrations of SOA ISO were similar at both sites (0.4 and 0.3 μg m-3, or 16% and 7%, at UB and RS, respectively). By contrast, a SOA biogenic component attributed to α-pinene oxidation (SOA BIO PIN) presented average concentrations of 0.5 μg m-3 at UB (24% of OA) and 0.2 μg m-3 at RS (7%), respectively, suggesting that this SOA component did not impact the two monitoring sites at the same level. A clear anti-correlation was observed between SOA ISO and SOA PIN during nucleation days, surprisingly suggesting that some of the growth of urban freshly nucleating particles may be driven by biogenic α-pinene oxidation products but inhibited by isoprene organic compounds. A third SOA component was formed by a mixture of aged anthropogenic and biogenic secondary organic compounds (SOA Aged) that accumulated under stagnant atmospheric conditions, contributing for 12% to OA at RS (0.4 μg OC m-3) and for 18% at UB (0.4 μg OC m-3). A sixth component, formed by C7-C9 dicarboxylic acids and detected especially during daytime, was called "urban oxygenated organic aerosol" (OOA Urban) due to its high abundance at urban RS (23%; 0.8 μg OCm-3) vs. UB (10%; 0.2 μg OCm-3), with a well-defined daytime maximum. This temporal trend and geographical differentiation suggests that local anthropogenic sources were determining this component. However, the changes of these organic molecules were also influenced by the air mass trajectories, indicating that atmospheric conditions have an influence on this component, although the specific origin on this component remains unclear. It points to a secondary organic component driven by primary urban sources including cooking and traffic (mainly gasoline) activities.
NASA Astrophysics Data System (ADS)
Alier, M.; van Drooge, B. L.; Dall'Osto, M.; Querol, X.; Grimalt, J. O.; Tauler, R.
2013-04-01
This study investigates the contribution of potential sources to the sub-micron (PM1) organic aerosol (OA) simultaneously detected at an urban background (UB) and a road site (RS) in Barcelona during the 30 days of the intensive field campaign of SAPUSS (Solving Aerosol Problems by Using Synergistic Strategies, September-October 2010). 103 filters at 12 h sampling time resolution were collected at both sites. Thirty-six neutral and polar organic compounds of known emission sources and photo-chemical transformation processes were analyzed by Gas Chromatography-Mass Spectrometry (GC-MS). The concentrations of the trace chemical compounds analyzed are herein presented and discussed. Additionally, OA source apportionment was performed by Multivariate Curve Resolution-Alternating Least Squares (MCR-ALS) and six OA components were identified at both sites: two were of primary anthropogenic OA origin, three of secondary OA origin while a sixth one was not clearly defined. Primary organics from emissions of local anthropogenic activities (Urban primary organic aerosol, Urban POA) contributed for 43% (1.5 μg OC m-3) and 18% (0.4 μg OC m-3) to OA in RS and UB, respectively. A secondary primary source - biomass burning (BBOA) - was found in all the samples (average values 7% RS; 12% UB; 0.3 μg OC m-3), but this component was substantially contributing to OA only when the sampling sites were under influence of regional air mass circulation. Three Secondary Organic Aerosol (SOA) components (describing overall 60% of the variance) were observed in the urban ambient PM1. Products of isoprene oxidation (SOA ISO), i.e. 2-methylglyceric acid, C5 alkene triols and 2-methyltetrols, showed the highest abundance at both sites when the city was under influence of inland air masses. The overall concentrations of SOA ISO were similar at both sites (0.4 and 0.3 μg m-3, 16% and 7%, at UB and RS, respectively). By contrast, a SOA biogenic component attributed to α-pinene oxidation (SOA BIO PIN) presented average concentrations of 0.5 μg m-3 at UB (24% of OA) and 0.2 μg m-3 at RS (7%), respectively, suggesting that this SOA component did not impact the two monitoring site at the same level. A clear anti correlation was observed between SOA ISO and SOA PIN during nucleation days, surprisingly suggesting that some of the growth of urban freshly nucleating particles may be driven by biogenic α-pinene oxidation products but inhibited by isoprene organic compounds. A third SOA component was formed by a mixture of aged anthropogenic and biogenic secondary organic compounds (Aged SOA) that accumulated under stagnant atmospheric conditions, contributing for 12% to OA at RS (0.4 μg OC m-3) and for 18% at UB (0.4 μg OC m-3). A sixth component, formed by C7-C9 dicarboxylic acids and detected especially during daytime, was called "urban oxygenated organic aerosol" (Urban OOA) due to its high abundance in urban RS (23%; 0.8 μg OC m-3) vs. UB (10%; 0.2 μg OC m-3), with a well-defined daytime maximum. This temporal trend and geographical differentiation suggests that local anthropogenic sources were determining this component. However, the changes of these organic molecules were also influenced by the air mass trajectories, indicating that atmospheric conditions had an influence on this component although the specific origin on this component remains unclear. It points to a secondary organic component driven by primary urban sources including cooking and traffic (mainly gasoline) activities.
NASA Astrophysics Data System (ADS)
Thorpe, A. K.; Frankenberg, C.; Thompson, D. R.; Duren, R. M.; Aubrey, A. D.; Bue, B. D.; Green, R. O.; Gerilowski, K.; Krings, T.; Borchardt, J.; Kort, E. A.; Sweeney, C.; Conley, S. A.; Roberts, D. A.; Dennison, P. E.; Ayasse, A.
2016-12-01
Imaging spectrometers like the next generation Airborne Visible/Infrared Imaging Spectrometer (AVIRIS-NG) can map large regions with the high spatial resolution necessary to resolve methane (CH4) and carbon dioxide (CO2) emissions. This capability is aided by real time detection and geolocation of gas plumes, permitting unambiguous identification of individual emission source locations and communication to ground teams for rapid follow up. We present results from AVIRIS-NG flight campaigns in the Four Corners region (Colorado and New Mexico) and the San Joaquin Valley (California). Over three hundred plumes were observed, reflecting emissions from anthropogenic and natural sources. Examples of plumes will be shown for a number of sources, including CH4 from well completions, gas processing plants, tanks, pipeline leaks, natural seeps, and CO2 from power plants. Despite these promising results, an imaging spectrometer built exclusively for quantitative mapping of gas plumes would have improved sensitivity compared to AVIRIS-NG. For example, an instrument providing a 1 nm spectral sampling (2,000-2,400 micron) would permit mapping CH4, CO2, H2O, CO, and N2O from more diffuse sources using both airborne and orbital platforms. The ability to identify emission sources offers the potential to constrain regional greenhouse gas budgets and improve partitioning between anthropogenic and natural emission sources. Because the CH4 lifetime is only about 9 years and CH4 has a Global Warming Potential 86 times that of CO2 for a 20 year time interval, mitigating these emissions is a particularly cost-effective approach to reduce overall atmospheric radiative forcing. Fig. 1. True color image subset with superimposed gas plumes showing concentrations in ppmm. Left: AVIRIS-NG observed CH4 plumes from natural gas processing plant extending over 500 m downwind of multiple emissions sources. Right: Multiple CO2 plumes observed from coal-fired power plant.
NASA Astrophysics Data System (ADS)
DesJardins, Michelle J.; Telmer, Kevin; Beauchamp, S.
Precipitation samples were collected from July 2001 through June 2002 to determine sources of anthropogenic heavy metal pollutants to Kejimkujik National Park, Nova Scotia using Pb isotope ratios. Generally, Mean annual Pb concentrations (0.116 μg l -1) and depositional fluxes (151 μg m -2) are lower than other reported mid-Atlantic coastal regions. Pb isotope compositions may be explained by binary mixing of anthropogenic emissions from US and Canadian sources, indicating long-range atmospheric transport of pollutants from populated and industrial regions of northeastern US and southeastern Canada. The 206Pb/ 207Pb ratios in precipitation ranged from 1.165 to 1.201, with an annual weighted mean 206Pb/ 207Pb ratio of 1.181, indicating that on an annual basis, US and Canadian sources contribute 61% and 39%, respectively, of the anthropogenic Pb (and likely other similarly behaved metal pollutants) reaching Kejimkujik Park. These results differ from those estimated by using epiphytic lichens due to one or a combination of the following possibilities: (1) some of the Pb in the lichens reflects more radiogenic local bedrock sources; (2) there has been an overall increase in the proportion of Canadian inputs since the early 1990s; (3) there was an unusually higher proportion of Pb inputs from Canadian sources during the study period; or (4) possible shifts in the isotopic composition of the Canadian and US sources that may have occurred due to increased international trade in lead and a lesser dependency on national production. As well, seasonal variations in the sources were observed, with summer and fall months having a lower mean 206Pb/ 207Pb ratio of 1.178 (more Canadian) than the winter and spring months with 206Pb/ 207Pb of 1.185 (more American).
Characterization of methane emissions in Los Angeles with airborne hyperspectral imaging
NASA Astrophysics Data System (ADS)
Saad, K.; Tratt, D. M.; Buckland, K. N.; Roehl, C. M.; Wennberg, P. O.; Wunch, D.
2017-12-01
As urban areas develop regulations to limit atmospheric methane (CH4), accurate quantification of anthropogenic emissions will be critical for program development and evaluation. However, relating emissions derived from process-level metadata to those determined from assimilating atmospheric observations of CH4 concentrations into models is particularly difficult. Non-methane hydrocarbons (NMHCs) can help differentiate between thermogenic and biogenic CH4 emissions, as they are primarily co-emitted with the former; however, these trace gases are subject to the same limitations as CH4. Remotely-sensed hyperspectral imaging bridges these approaches by measuring emissions plumes directly with spatial coverage on the order of 10 km2 min-1. We identify the sources of and evaluate emissions plumes measured by airborne infrared hyperspectral imagers flown over the Los Angeles (LA) metropolitan area, which encompasses various CH4 sources, including petroleum and natural gas wells and facilities. We quantify total CH4 and NMHC emissions, as well as their relative column densities, at the point-source level to create fingerprints of source types. We aggregate these analyses to estimate the range of variability in chemical composition across source types. These CH4 and NMHC emissions factors are additionally compared to their tropospheric column abundances measured by the Total Carbon Column Observing Network (TCCON) Pasadena Fourier transform infrared spectrometer, which provides a footprint for the LA basin.
Local sources of pollution and their impacts in Alaska (Invited)
NASA Astrophysics Data System (ADS)
Molders, N.
2013-12-01
The movie 'Into the Wilde' evoke the impression of the last frontier in a great wide and pristine land. With over half a million people living in Alaska an area as larger as the distance from the US West to the East Coast, this idea comes naturally. The three major cities are the main emission source in an otherwise relative clean atmosphere. On the North Slope oil drilling and production is the main anthropogenic emission sources. Along Alaska's coasts ship traffic including cruises is another anthropogenic emission source that is expected to increase as sea-ice recedes. In summer, wildfires in Alaska, Canada and/or Siberia may cause poor air quality. In winter inversions may lead poor air quality and in spring. In spring, aged polluted air is often advected into Alaska. These different emission sources yield quite different atmospheric composition and air quality impacts. While this may make understanding Alaska's atmospheric composition at-large a challenging task, it also provides great opportunities to examine impacts without co-founders. The talk will give a review of the performed research, and insight into the challenges.
NASA Astrophysics Data System (ADS)
Jandačka, Dušan
2015-05-01
Particulate matter results as an aftermath of numerous distinctive processes in the atmosphere and they become a part of everyday life. Their harmful effect and impact on the ambient environment is determined predominantly by the presence of various chemical substances and elements. The chemical composition of these particles (organic and elemental carbon, mineral dust, sea aerosols, secondary particles, especially sulphates and nitrates, heavy metals and further elements) is mainly impacted on by their origin, whereas the primary source of the particulate matter is determined and specified by the profile of chemical elements and substances. Particulate Matter (PM) may originate in various natural resources or anthropogenic sources. Among the natural sources sea salt is to be counted on, dust of the earth crust, pollen and volcanic ashes. Anthropogenic sources do include, predominantly, burning fossil fuels in the fossil-fuel power plants, local heating of households, burning liquefied fossil fuels in the combustion engines of vehicles, noncombustion related emissions as a result of vehicular traffic, resuspension of the road-traffic-related dust.
A temporal and spatial analysis of anthropogenic noise sources affecting SNMR
NASA Astrophysics Data System (ADS)
Dalgaard, E.; Christiansen, P.; Larsen, J. J.; Auken, E.
2014-11-01
One of the biggest challenges when using the surface nuclear magnetic resonance (SNMR) method in urban areas is a relatively low signal level compared to a high level of background noise. To understand the temporal and spatial behavior of anthropogenic noise sources like powerlines and electric fences, we have developed a multichannel instrument, noiseCollector (nC), which measures the full noise spectrum up to 10 kHz. Combined with advanced signal processing we can interpret the noise as seen by a SNMR instrument and also obtain insight into the more fundamental behavior of the noise. To obtain a specified acceptable noise level for a SNMR sounding the stack size can be determined by quantifying the different noise sources. Two common noise sources, electromagnetic fields stemming from powerlines and fences are analyzed and show a 1/r2 dependency in agreement with theoretical relations. A typical noise map, obtained with the nC instrument prior to a SNMR field campaign, clearly shows the location of noise sources, and thus we can efficiently determine the optimal location for the SNMR sounding from a noise perspective.
NASA Astrophysics Data System (ADS)
Hardiman, B. S.; Hutyra, L.; Gately, C.; Raciti, S. M.
2014-12-01
Urban areas are home to 80% of the US population and 70% of energy related fossil fuel emissions originate from urban areas. Efforts to accurately monitor, report, and verify anthropogenic CO2 missions using atmospheric measurements require reliable partitioning of anthropogenic and biogenic sources. Anthropogenic emissions peak during the daytime, coincident with biogenic drawdown of CO2. In contrast, biogenic respiration emissions peak at night when anthropogenic emissions are lower. This temporal aliasing of fluxes requires careful modeling of both biogenic and anthropogenic fluxes for accurate source attribution through inverse modeling. Biogenic fluxes in urban regions can be a significant component of the urban carbon cycle. However, vegetation in urban areas is subject to longer growing seasons, reduced competition, higher rates of nitrogen deposition, and altered patterns of biomass inputs, all interacting to elevate C turnover rates relative to analogous non-urban ecosystems. These conditions suggest that models that ignore urban vegetation or base biogenic flux estimates on non-urban forests are likely to produce inaccurate estimates of anthropogenic CO2 emissions. Biosphere models often omit biogenic fluxes in urban areas despite potentially extensive vegetation coverage. For example, in Massachusetts, models mask out as much as 40% of land area, effectively assuming they have no biological flux. This results in a ~32% underestimate of aboveground biomass (AGB) across the state as compared to higher resolution vegetation maps. Our analysis suggests that some common biomass maps may underestimate forest biomass by ~520 Tg C within the state of Massachusetts. Moreover, omitted portions of the state have the highest population density, indicating that we know least about regions where most people live. We combine remote sensing imagery of urban vegetation cover with ground surveys of tree growth and mortality to improve estimates of aboveground biomass and biogenic flux rates. Updated biogenic flux rates are combined with spatially explicit anthropogenic flux estimates and a network of urban CO2 monitoring sites as the foundation for a novel carbon monitoring system spanning the Boston-Washington D.C. metropolitan corridor.
Assessing heavy metal sources in sugarcane Brazilian soils: an approach using multivariate analysis.
da Silva, Fernando Bruno Vieira; do Nascimento, Clístenes Williams Araújo; Araújo, Paula Renata Muniz; da Silva, Luiz Henrique Vieira; da Silva, Roberto Felipe
2016-08-01
Brazil is the world's largest sugarcane producer and soils in the northeastern part of the country have been cultivated with the crop for over 450 years. However, so far, there has been no study on the status of heavy metal accumulation in these long-history cultivated soils. To fill the gap, we collect soil samples from 60 sugarcane fields in order to determine the contents of Cd, Cr, Cu, Ni, Pb, and Zn. We used multivariate analysis to distinguish between natural and anthropogenic sources of these metals in soils. Analytical determinations were performed in ICP-OES after microwave acid solution digestion. Mean concentrations of Cd, Cr, Cu, Ni, Pb, and Zn were 1.9, 18.8, 6.4, 4.9, 11.2, and 16.2 mg kg(-1), respectively. The principal component one was associated with lithogenic origin and comprised the metals Cr, Cu, Ni, and Zn. Cluster analysis confirmed that 68 % of the evaluated sites have soil heavy metal concentrations close to the natural background. The Cd concentration (principal component two) was clearly associated with anthropogenic sources with P fertilization being the most likely source of Cd to soils. On the other hand, the third component (Pb concentration) indicates a mixed origin for this metal (natural and anthropogenic); hence, Pb concentrations are probably related not only to the soil parent material but also to industrial emissions and urbanization in the vicinity of the agricultural areas.
NASA Astrophysics Data System (ADS)
Parazoo, N.; Bowman, K. W.; Kuai, L.; Liu, J.; Lee, M.; Baker, I. T.; Berry, J. A.; Davis, K. J.; Lauvaux, T.; DiGangi, J. P.; Sweeney, C.
2017-12-01
Multi-species measurements of CO, OCS, and SIF have the potential to attribute CO2 variability to productivity and anthropogenic emissions. ACT-America aircraft campaigns in summer 2016 and winter 2017 collected vertical profiles of these key species close to their sources, providing important constraints on CO2 sources across 3 unique regions in eastern North America. The CMS-Flux carbon cycle assimilation system uses satellite measurements of CO (MOPITT), CO2 (OCO-2), SIF (OCO-2), and OCS (TES) to determine regional CO2 sources due to fossil fuel emissions, biomass burning, and net biome exchange, providing independent flux constraints, and which can be propagated back to the atmosphere for direct comparison to aircraft data. Here, we evaluate tracer-tracer correlations between CO2, CO, and OCS from ACT-America aircraft data during fall and winter campaigns, and compare to posterior signals from CMS-Flux over the same period. To predict atmospheric OCS signals, we leverage mechanistic representations of OCS plant uptake and GPP in the SiB land surface model to determine OCS-GPP linear relationships, then use SIF optimized estimates of GPP to infer OCS fluxes. Our objectives in this study are 3 fold: (1) Determine consistency of regional source attributions from CMS-Flux with aircraft data from ACT-America; (2) Analyze observed (ACT-America) and predicted (CMS-Flux) tracer-tracer correlations across multiple seasons and regions to identify key biogenic and anthropogenic drivers; (3) Determine to what extent SIF and OCS are valid linear predictors of GPP spatial variability. Summertime evaluation of these tracers shows good correlation between OCS/CO2 and OCS/CO in the midwest but poorer correlation in the northeast possibly reflecting biogenic controls on CO2. Comparisons of observed and predicted CO and CO2 in the PBL with CMF-Flux data indicate positively correlated biases that reflect both transport and flux errors. These results are compared with the winter campaign data to better inform biogenic vs anthropogenic sources, and provide ensemble predictions of OCS from SiB and multi-satellite SIF constraints for more robust analysis of GPP variability.
Relative importance of atmospheric and riverine mercury sources to the northern Gulf of Mexico.
Rice, Glenn E; Senn, David B; Shine, James P
2009-01-15
A box model was developed to quantify the major sources and dominant fates of inorganic mercury (Hg) in the Mississippi River-influenced area of the northern Gulf of Mexico (nGOM). Riverine (75%) and direct atmospheric deposition (25%) deliver 9.7 t Hg y(-1) to this productive fishery; most (80%) accumulates in bottom sediments where it can be methylated and enter foodwebs. Although riverine inputs dominate atmospheric deposition, 75% of the riverine sediment-associated Hg accumulates in only approximately 8% of the study area. Atmospheric deposition can explain most of the Hg accumulating in sediments of the remaining area. Considering the differences in temporal responsiveness of riverine (centuries) and atmospheric (years) Hg inputs to anthropogenic emissions changes, the spatial limits of the riverine Hg source andthe potential dominance of atmospheric deposition over large areas could have implications for the timing of benefits from policies reducing anthropogenic Hg emissions.
The DRAGON scale concept and results for remote sensing of aerosol properties
NASA Astrophysics Data System (ADS)
Holben, B. N.; Eck, T. F.; Schafer, J.; Giles, D. M.; Kim, J.; Sano, I.; Mukai, S.; Kim, Y. J.; Reid, J. S.; Pickering, K. E.; Crawford, J. H.; Smirnov, A.; Sinyuk, A.; Slutsker, I.; Sorokin, M.; Rodriguez, J.; Liew, S.; Trevino, N.; Lim, H.; Lefer, B. L.; Nadkarni, R.; Macke, A.; Kinne, S. A.; Anderson, B. E.; Russell, P. B.; Maring, H. B.; Welton, E. J.; da Silva, A.; Toon, O. B.; Redemann, J.
2013-12-01
Aerosol processes occur at microscales but are typically observed and reported at continental to global scales. Often observable aerosol processes that have significant anthropogenic impact occur on spatial scales of tens to a few hundred km, representative of convective cloud processing, urban/megacity sources, anthropogenic burning and natural wildfires, dry lakebed dust sources etc. Historically remote sensing of aerosols has relied on relatively coarse temporal and spatial resolution satellite observations or high temporal resolution point observations from ground-based monitoring sites from networks such as AERONET, SKYNET, MPLNET and many other surface observation platforms. Airborne remote and in situ observations combined with assimilation models were/are to be the mesoscale link between the ground- and space-based RS scales. However clearly the in situ and ground-based RS characterizations of aerosols require a convergence of thought, parameterization and actual scale measurements in order to advance this goal. This has been served by periodic multidisciplinary field campaigns yet only recently has a concerted effort been made to establish these ground-based networks in an effort to capture the mesoscale processes through measurement programs such as DISCOVER AQ and NASA AERONET's effort to foster such measurements and analysis through the Distributed Regional Aerosol Gridded Observation Networks (DRAGON), short term meso-networks, with partners in Asia and Europe and N. America. This talk will review the historical need for such networks and discuss some of the results and in some cases unexpected findings from the eight DRAGON campaigns conducted the last several years. Emphasis will be placed on the most recent DISCOVER AQ campaign conducted in Houston TX and the synergism with a regional to global network plan through the SEAC4RS US campaign.
Current and future levels of mercury atmospheric pollution on a global scale
NASA Astrophysics Data System (ADS)
Pacyna, Jozef M.; Travnikov, Oleg; De Simone, Francesco; Hedgecock, Ian M.; Sundseth, Kyrre; Pacyna, Elisabeth G.; Steenhuisen, Frits; Pirrone, Nicola; Munthe, John; Kindbom, Karin
2016-10-01
An assessment of current and future emissions, air concentrations, and atmospheric deposition of mercury worldwide is presented on the basis of results obtained during the performance of the EU GMOS (Global Mercury Observation System) project. Emission estimates for mercury were prepared with the main goal of applying them in models to assess current (2013) and future (2035) air concentrations and atmospheric deposition of this contaminant. The combustion of fossil fuels (mainly coal) for energy and heat production in power plants and in industrial and residential boilers, as well as artisanal and small-scale gold mining, is one of the major anthropogenic sources of Hg emissions to the atmosphere at present. These sources account for about 37 and 25 % of the total anthropogenic Hg emissions globally, estimated to be about 2000 t. Emissions in Asian countries, particularly in China and India, dominate the total emissions of Hg. The current estimates of mercury emissions from natural processes (primary mercury emissions and re-emissions), including mercury depletion events, were estimated to be 5207 t year-1, which represents nearly 70 % of the global mercury emission budget. Oceans are the most important sources (36 %), followed by biomass burning (9 %). A comparison of the 2035 anthropogenic emissions estimated for three different scenarios with current anthropogenic emissions indicates a reduction of these emissions in 2035 up to 85 % for the best-case scenario. Two global chemical transport models (GLEMOS and ECHMERIT) have been used for the evaluation of future mercury pollution levels considering future emission scenarios. Projections of future changes in mercury deposition on a global scale simulated by these models for three anthropogenic emissions scenarios of 2035 indicate a decrease in up to 50 % deposition in the Northern Hemisphere and up to 35 % in Southern Hemisphere for the best-case scenario. The EU GMOS project has proved to be a very important research instrument for supporting the scientific justification for the Minamata Convention and monitoring of the implementation of targets of this convention, as well as the EU Mercury Strategy. This project provided the state of the art with regard to the development of the latest emission inventories for mercury, future emission scenarios, dispersion modelling of atmospheric mercury on a global and regional scale, and source-receptor techniques for mercury emission apportionment on a global scale.
Coynel, Alexandra; Blanc, Gérard; Marache, Antoine; Schäfer, Jörg; Dabrin, Aymeric; Maneux, Eric; Bossy, Cécile; Masson, Matthieu; Lavaux, Gilbert
2009-05-01
The Riou Mort River watershed (SW France), representative of a heavily polluted, small, heterogeneous watershed, represents a major source for the polymetallic pollution of the Lot-Garonne-Gironde fluvial-estuarine system due to former mining and ore-treatment activities. In order to assess spatial distribution of the metal/metalloid contamination in the watershed, a high resolution hydrological and geochemical monitoring were performed during one year at four permanent observation stations. Additionally, thirty-five stream sediment samples were collected at representative key sites and analyzed for metal/metalloid (Cd, Zn, Cu, Pb, As, Sb, Mo, V, Cr, Co, Ni, Th, U and Hg) concentrations. The particulate concentrations in water and stream sediments show high spatial differences for most of the studied elements suggesting strong anthropogenic and/or lithogenic influences; for stream sediments, the sequence of the highest variability, ranging from 100% to 300%, is the following: Mo < Cu < Hg < As < Sb < Cd < Zn < Pb. Multidimensional statistical analyses combined with metal/metalloid maps generated by GIS tool were used to establish relationships between elements, to identify metal/metalloid sources and localize geochemical anomalies attributed to local geochemical background, urban and industrial activities. Finally, this study presents an approach to assess anthropogenic trace metal inputs within this watershed by combining lithology-dependent geochemical background values, metal/metalloid concentrations in stream sediments and mass balances of element fluxes at four key sites. The strongest anthropogenic contributions to particulate element fluxes are 90-95% for Cd, Zn and Hg in downstream sub-catchments. The localisation of anthropogenic metal/metalloid sources in restricted areas offers a great opportunity to further significantly reduce metal emissions and restore the Lot-Garonne-Gironde fluvial-estuarine ecosystem.
Loretto, Matthias-Claudio; Schuster, Richard; Bugnyar, Thomas
2016-08-01
In many songbirds, the space use of breeders is well studied but poorly understood for non-breeders. In common ravens, some studies of non-breeders indicate high vagrancy with large individual differences in home range size, whereas others show that up to 40% of marked non-breeders can be regularly observed at the same anthropogenic food source over months to years. The aim of this study was to provide new insights on ravens' behavior during dispersal in the Eastern Alps. We deployed Global Positioning System (GPS) loggers on 10 individuals to gather accurate spatial and temporal information on their movements to quantify: 1) the dimension of the birds' space use (home range size with seasonal effects and daily/long-term travel distances), 2) how long they stayed in a dispersal stage of wandering as opposed to settling temporarily, and 3) their destination of movements. We recorded movements of up to 40 km per hour, more than 160 km within 1 day and more than 11,000 km within 20 months, indicating high vagrancy. Switching frequently between temporarily settling and travelling large distances in short time intervals leads to extensive home ranges, which also explains and combines the different findings in the literature. The destinations are rich anthropogenic food sources, where the birds spent on average 75% of their time. We discuss how ravens may find these "feeding hot spots" and which factors may influence their decision to stay/leave a site. The strong dependence on anthropogenic resources found in this population may have implications for site management and conservation issues.
NASA Astrophysics Data System (ADS)
Alexander, Becky; Park, Rokjin J.; Jacob, Daniel J.; Gong, Sunling
2009-01-01
We use observations of the oxygen-17 excess (Δ17O) of sulfate in the Arctic to quantify the sulfate source from aqueous SO2 (S(IV)) oxidation by O2 catalyzed by transition metals. Due to the lack of photochemically produced OH and H2O2 in high latitudes during winter, combined with high anthropogenic SO2 emissions in the Northern Hemisphere, oxidation by O3 is predicted to dominate sulfate formation during winter in this region. However, Δ17O measurements of sulfate aerosol collected in Alert, Canada, are not consistent with O3 as the dominant oxidant and indicate that a S(IV) oxidant with near-zero Δ17O values (O2) is important during winter. We use a global chemical transport model to interpret quantitatively the Alert observations and assess the global importance of sulfate production by Fe(III)- and Mn(II)-catalyzed oxidation of S(IV) by O2. We scale anthropogenic and natural atmospheric metal concentrations to primary anthropogenic sulfate and dust concentrations, respectively. The solubility and oxidation state of these metals is determined by cloud liquid water content, source, and sunlight. By including metal-catalyzed S(IV) oxidation, the model is consistent with the Δ17O magnitudes in the Alert data during winter. Globally, we find that this mechanism contributes 9-17% to sulfate production. The inclusion of metal-catalyzed oxidation does not resolve model discrepancies with surface SO2 and sulfate observations in Europe. Oxygen isotope measurements of sulfate aerosols collected near anthropogenic and dust sources of metals would help to verify the importance of this sulfur oxidation pathway.
NASA Astrophysics Data System (ADS)
Adak, Anandamay; Chatterjee, Abhijit; Ghosh, Sanjay; Raha, Sibaji; Roy, Arindam
2016-07-01
A study was conducted on the chemical characterization of fine mode aerosol or PM2.5 over a rural atmosphere near the coast of Bay of Bengal in eastern India. Samples were collected and analyzed during March 2013 - February 2014. The concentration of PM2.5 was found span over a wide range from as low as 3 µg m-3 to as high as 180 µg m-3. The average concentration of PM2.5 was 62 µg m-3. Maximum accumulation of fine mode aerosol was observed during winter whereas minimum was observed during monsoon. Water soluble ionic species of fine mode aerosol were characterized over this rural atmosphere. In spite of being situated near the coast of Bay of Bengal, we observed significantly higher concentrations for anthropogenic species like ammonium and sulphate. The concentrations of these two species were much higher than the sea-salt aerosols. Ammonium and sulphate contributed around 30 % to the total fine mode aerosols. Even dust aerosol species like calcium also showed higher concentrations. Chloride to sodium ratio was found to be much less than that in standard sea-water indicating strong interaction between sea-salt and anthropogenic aerosols. Use of fertilizers in various crop fields and human and animal wastes significantly increased ammonium in fine mode aerosols. Dust aerosol species were accumulated in the atmosphere which could be due to transport of finer dust species from nearby metropolis or locally generated. Non-sea-sulphate and nitrate showed significant contributions in fine mode aerosols having both local and transported sources. Source apportionment shows prominent emission sources of anthropogenic aerosols from local anthropogenic activities and transported from nearby Kolkata metropolis as well.
NASA Astrophysics Data System (ADS)
Qian, J.; He, Q.
2014-12-01
This paper developed a high resolution emission inventory of major pollutants in city cluster of Sichuan Basin, one of the most polluted regions in China. The city cluster included five cities, which were Chengdu, Deyang, Mianyang, Meishan and Ziyang. Pollution source census and field measurements were conducted for the major emission sources such as the industry sources, on-road mobile sources, catering sources and the dust sources. The inventory results showed that in the year of 2012, the emission of SO2、NOX、CO、PM10、PM2.5、VOCs and NH3 in the region were 143.5、251.9、1659.9、299.3、163.5、464.1 and 995kt respectively. Chengdu, the provincial capital city, had the largest emission load of every pollutant among the cities. The industry sources, including power plants, fuel combustion facilities and non-combustion processes were the largest emission sources for SO2、NOX and CO, contributing to 84%, 46.5%, 35% of total SO2, NOX and CO emissions. On-road mobile sources accounted for 46.5%, 33%, 16% of the total NOx, CO, PM2.5 emissions and 28% of the anthropogenic VOCs emission. Dust and industry sources contributed to 42% and 23% of the PM10 emission with the dust sources also as the largest source of PM2.5, contributing to 27%. Anthropogenic and biogenic sources took 75% and 25% of the total VOCs emission while 36% of anthropogenic VOCs emission was owing to solvent use. Livestock contributed to 62% of NH3 emissions, followed by nitrogen fertilizer application whose contribution was 23%. Based on the developed emission inventory and local meteorological data, the regional air quality modeling system WRF-CMAQ was applied to simulate the status of PM2.5 pollution in a regional scale. The results showed that high PM2.5 concentration was distributed over the urban area of Chengdu and Deyang. On-road mobile sources and dust sources were two major contributors to the PM2.5 pollution in Chengdu, both had an contribution ratio of 27%. In Deyang, Mianyang, Meishan and Ziyang, industry sources had a relatively high contribution ratio to the PM2.5 pollution, accounting for about 35%, 33%, 38% and 24% respectively.
Ogle, Stephen M; Domke, Grant; Kurz, Werner A; Rocha, Marcelo T; Huffman, Ted; Swan, Amy; Smith, James E; Woodall, Christopher; Krug, Thelma
2018-05-29
Land use and management activities have a substantial impact on carbon stocks and associated greenhouse gas emissions and removals. However, it is challenging to discriminate between anthropogenic and non-anthropogenic sources and sinks from land. To address this problem, the Intergovernmental Panel on Climate Change developed a managed land proxy to determine which lands are contributing anthropogenic greenhouse gas emissions and removals. Governments report all emissions and removals from managed land to the United Nations Framework Convention on Climate Change based on this proxy, and policy interventions to reduce emissions from land use are expected to focus on managed lands. Our objective was to review the use of the managed land proxy, and summarize the criteria that governments have applied to classify land as managed and unmanaged. We found that the large majority of governments are not reporting on their application of the managed land proxy. Among the governments that do provide information, most have assigned all area in specific land uses as managed, while designating all remaining lands as unmanaged. This designation as managed land is intuitive for croplands and settlements, which would not exist without management interventions, but a portion of forest land, grassland, and wetlands may not be managed in a country. Consequently, Brazil, Canada and the United States have taken the concept further and delineated managed and unmanaged forest land, grassland and wetlands, using additional criteria such as functional use of the land and accessibility of the land to anthropogenic activity. The managed land proxy is imperfect because reported emissions from any area can include non-anthropogenic sources, such as natural disturbances. However, the managed land proxy does make reporting of GHG emissions and removals from land use more tractable and comparable by excluding fluxes from areas that are not directly influenced by anthropogenic activity. Moreover, application of the managed land proxy can be improved by incorporating additional criteria that allow for further discrimination between managed and unmanaged land.
Impact of seaweed beachings on dynamics of δ(15)N isotopic signatures in marine macroalgae.
Lemesle, Stéphanie; Mussio, Isabelle; Rusig, Anne-Marie; Menet-Nédélec, Florence; Claquin, Pascal
2015-08-15
A fine-scale survey of δ(15)N, δ(13)C, tissue-N in seaweeds was conducted using samples from 17 sampling points at two sites (Grandcamp-Maisy (GM), Courseulles/Mer (COU)) along the French coast of the English Channel in 2012 and 2013. Partial triadic analysis was performed on the parameter data sets and revealed the functioning of three areas: one estuary (EstA) and two rocky areas (GM(∗), COU(∗)). In contrast to oceanic and anthropogenic reference points similar temporal dynamics characterized δ(15)N signatures and N contents at GM(∗) and COU(∗). Nutrient dynamics were similar: the N-concentrations in seawater originated from the River Seine and local coastal rivers while P-concentrations mainly from these local rivers. δ(15)N at GM(∗) were linked to turbidity suggesting inputs of autochthonous organic matter from large-scale summer seaweed beachings made up of a mixture of Rhodophyta, Phaeophyta and Chlorophyta species. This study highlights the coupling between seaweed beachings and nitrogen sources of intertidal macroalgae. Copyright © 2015 Elsevier Ltd. All rights reserved.
Miller, Helen; Croudace, Ian W; Bull, Jonathan M; Cotterill, Carol J; Dix, Justin K; Taylor, Rex N
2014-07-01
A high-resolution record of pollution is preserved in recent sediments from Windermere, the largest lake in the English Lake District. Data derived from X-ray core scanning (validated against wavelength dispersive X-ray fluorescence), radiochronological techniques ((210)Pb and (137)Cs) and ultrahigh precision, double-spike mass spectrometry for lead isotopes are combined to decipher the anthropogenic inputs to the lake. The sediment record suggests that while most element concentrations have been stable, there has been a significant increase in lead, zinc, and copper concentrations since the 1930s. Lead isotope down-core variations identify three major contributory sources of anthropogenic (industrial) lead, comprising gasoline lead, coal combustion lead (most likely source is coal-fired steam ships), and lead derived from Carboniferous Pb-Zn mineralization (mining activities). Periods of metal workings do not correlate with peaks in heavy metals due to the trapping efficiency of up-system lakes in the catchment. Heavy metal increases could be due to flood-induced metal inwash after the cessation of mining and the weathering of bedrock in the catchment. The combination of sediment analysis techniques used provides new insights into the pollutant depositional history of Windermere and could be similarly applied to other lake systems to determine the timing and scale of anthropogenic inputs.
McGann, Mary; Erikson, Li H.; Wan, Elmira; Powell, Charles; Maddocks, Rosalie F.; Barnard, P.L.; Jaffee, B.E.; Schoellhamer, D.H.
2013-01-01
Although conventional sediment parameters (mean grain size, sorting, and skewness) and provenance have typically been used to infer sediment transport pathways, most freshwater, brackish, and marine environments are also characterized by abundant sediment constituents of biological, and possibly anthropogenic and volcanic, origin that can provide additional insight into local sedimentary processes. The biota will be spatially distributed according to its response to environmental parameters such as water temperature, salinity, dissolved oxygen, organic carbon content, grain size, and intensity of currents and tidal flow, whereas the presence of anthropogenic and volcanic constituents will reflect proximity to source areas and whether they are fluvially- or aerially-transported. Because each of these constituents have a unique environmental signature, they are a more precise proxy for that source area than the conventional sedimentary process indicators. This San Francisco Bay Coastal System study demonstrates that by applying a multi-proxy approach, the primary sites of sediment transport can be identified. Many of these sites are far from where the constituents originated, showing that sediment transport is widespread in the region. Although not often used, identifying and interpreting the distribution of naturally-occurring and allochthonous biologic, anthropogenic, and volcanic sediment constituents is a powerful tool to aid in the investigation of sediment transport pathways in other coastal systems.
A COMPARISON OF METHODS FOR ESTIMATING GLOBAL METHANE EMISSIONS FROM LANDFILLS
Landfills are a significant source of methane, ranking third in anthropogenic sources after rice paddies and ruminants. Estimating the contribution of landfills to global methane flux is hampered by a lack of accurate refuse and landfill data, and therefore depends heavily on the...
Urban surface waters can be impacted by anthropogenic sources such as impervious surfaces, sanitary and storm sewers, and failing infrastructure. Fecal indicator bacteria (FIB) and microbial source tracking (MST) markers are common gauges of stream water quality, however, little...
ROLE OF OCEANIC AND RIVERINE SOURCES IN NUTRIENT AND PHYTOPLANKTON DYNAMICS IN YAQUINA BAY, OREGON
There is evidence that coastal ecosystems are experiencing environmental problems due to excess nutrients. The numerous sources, forms, and pathways of nutrients make it difficult to determine the effect of increases in anthropogenic loading. This is particularly evident in Pac...
NASA Astrophysics Data System (ADS)
Scarelli, Frederico M.; Cantelli, Luigi; Barboza, Eduardo G.; Gabbianelli, Giovanni
2017-05-01
This paper focuses on the Ural Delta in the northern zone of the Caspian Sea, an area with particular characteristics, where intense influence from anthropogenic and natural factors exists, which acts on the fragile delta system. We built a database to integrate the data from the published sources, bathymetric survey, and recent images in the geographical information system (GIS) environment. The results were linked to the Caspian Sea level (CSL) curve, which had many variations, changing the Ural Delta system's dynamics and in its architecture. In addition, the anthropogenic changes contribute to shaping the actual Ural Delta architecture. Through the link between the results and CSL, we reconstructed an evolution model for the Ural Delta system for the last century and identified three different architectures for the Ural Delta, determined by the energy that acted on the system in the last century and by the anthropogenic changes. This work identifies six different delta phases, which are shaped by CSL changes during the last 70 years and by anthropogenic changes. The delta phases recognized are: i) a Lobate Delta phase, shaped during high CSL before 1935; ii) Natural Elongate Delta 1935-1950 formed during rapid CSL fall; iii) Anthropogenic Elongate Delta 1950-1966, formed during rapid CSL fall and after the Ural-Caspian Sea canal construction, which modified the sedimentary deposition on the delta; iv) Anthropogenic Elongate Delta 1966-1982 shaped during low CSL phase; v) Anthropogenic Elongate Delta 1982-1996 formed during a rapid CSL rise phase; and vi) Anthropogenic Elongate Delta 1996-2009 shaped during high CSL that represent the last phase and actual Ural Delta architecture.
NASA Astrophysics Data System (ADS)
Fischbeck, Garlich; Neumaier, Marco; Safadi, Layal; Zahn, Andreas
2016-04-01
Since 2005 a Lufthansa passenger aircraft is regularly used as a platform for in-situ measurements in the upper troposphere and lowermost stratosphere (UTLMS). Accommodated in a modified airfreight container 15 instruments are deployed in the cargo bay of the aircraft on four selected intercontinental flights per month measuring ~100 species and aerosol parameters. In contrast to other projects of this scope, using a chemical mass spectrometer also volatile organic compounds like acetone (CH3COCH3) and acetonitrile (CH3CN) are detected enabling an investigation of their relationship with other tracers. On a global scale acetone is predominantly emitted from the biosphere (~37 Tg/a; MEGAN-MACC, Sinderarova et al. 2014) and comparably small amounts are directly emitted from biomass burning (~2 Tg/a; GFED3, Van der Werf et al. 2010) and other anthropogenic sources (~1 Tg/a; MACCity, Granier et al. 2011). However, at local levels the contributions from the different sources can strongly differ. Acetone is also secondarily produced in the atmosphere by the oxidation of various precursors, e.g. pinene and propane. The emissions of these precursors and their contribution to the total acetone source are not well known and a topic of ongoing discussions. In this context it is initially surprising that generally a good correlation between acetone and carbon monoxide (CO) has been observed in the lower atmosphere by different authors (e.g. de Reus et al. 2003). As a product of incomplete combustion CO is regularly used as a tracer for anthropogenic pollution and biomass burning. In this study we present an improved method to detect local correlations in IAGOS-CARIBIC flights instead of mixing data from different flights or measured over great distances. Furthermore, a cluster analysis is applied to prevent the consideration of artificial correlations between two well separated clouds of data points. We use the concept of enhancement ratios (EnR) and a simple box model to interpret the correlations. Based on this model we investigate the temporal evolution of EnR and find out that an increase of acetone-CO-EnR with time is common for many scenarios and does not necessarily require secondary production of acetone. Applying our method and criteria to the full IAGOS-CARIBIC dataset reveals that 50 per cent of the available tropospheric acetone data shows a local correlation (correlation coefficient r ≥ 0.5) with CO. In the Northern hemisphere subtropics and midlatitudes (23.5°N - 66.5°N) we find mean EnR of (17.8 ± 9.1) pptv/ppbv in summer and (9.4 ± 4.0) pptv/ppbv in winter. In air masses sampled above or originating from North America the seasonal cycle is more pronounced with a median EnR of 28.9 pptv/ppbv in summer and 10.1 pptv/ppbv in winter. This is in good agreement with the ratio of the total North American emissions of acetone and CO according to inventories from the ECCAD database. For East Asia EnR are low throughout the year and show only a weak annual cycle with a median of 12.4 pptv/ppbv in summer and 10.9 pptv/ppbv in winter. This can be tracked back to higher CO emissions from anthropogenic pollution. The presented findings point out that tropospheric EnR vary considerably depending on season, region and age of air mass, but have great potential to assess the ensemble of regional acetone and CO sources.
Nduka, J. K. C.; Orisakwe, O. E.; Ezenweke, L. O.; Ezenwa, T. E.; Chendo, M. N.; Ezeabasili, N. G.
2008-01-01
Rain samples were collected from Warri and Port Harcourt, two major oil-producing cities of Nigeria in April-June, July-August, and September-October 2005 and 2006. Awka, a “non-oil” city was used as control. Samples were collected from three points, using clean plastic basins fastened to a table, 2 m above ground level and 115 m away from tall buildings and trees. Water samples were filtered and acidity determined using digital pHmeter. The results show that the rain samples were acidic. The pH values for the 2 years under study show that the rainfall in Warri was more acidic than that of Port Harcourt. Oil exploration and other anthropogenic sources may be responsible for the acid rain in the Niger Delta region of Nigeria. PMID:18758657
Nduka, J K C; Orisakwe, O E; Ezenweke, L O; Ezenwa, T E; Chendo, M N; Ezeabasili, N G
2008-08-28
Rain samples were collected from Warri and Port Harcourt, two major oil-producing cities of Nigeria in April-June, July-August, and September-October 2005 and 2006. Awka, a "non-oil" city was used as control. Samples were collected from three points, using clean plastic basins fastened to a table, 2 m above ground level and 115 m away from tall buildings and trees. Water samples were filtered and acidity determined using digital pH meter. The results show that the rain samples were acidic. The pH values for the 2 years under study show that the rainfall in Warri was more acidic than that of Port Harcourt. Oil exploration and other anthropogenic sources may be responsible for the acid rain in the Niger Delta region of Nigeria.
Poor health is associated with use of anthropogenic resources in an urban carnivore.
Murray, Maureen; Edwards, Mark A; Abercrombie, Bill; St Clair, Colleen Cassady
2015-05-07
Rates of encounters between humans and wildlife are increasing in cities around the world, especially when wildlife overlap with people in time, space and resources. Coyotes (Canis latrans) can make use of anthropogenic resources and reported rates of conflict have increased in cities across North America. This increase may be linked to individual differences in the use of human food and developed areas. We compared the relationships between coyote age, sex or health and the use of anthropogenic resources, which we defined as using developed areas over large home ranges, being active during the day, and consuming anthropogenic food. To do so, we applied GPS collars to 19 coyotes and sampled hair for stable isotope analysis. Eleven coyotes appeared to be healthy and eight were visibly infested with sarcoptic mange (Sarcoptes scabiei), a mite that causes hair loss. Diseased coyotes used more developed areas, had larger monthly home ranges, were more active during the day, and assimilated less protein than coyotes that appeared to be healthy. We speculate that anthropogenic food provides a low-quality but easily accessible food source for diseased coyotes, which in turn may increase reliance on it and other anthropogenic resources to promote encounters with people. © 2015 The Author(s) Published by the Royal Society. All rights reserved.
A geological reconnaissance of electrical and electronic waste as a source for rare earth metals.
Mueller, Sandra R; Wäger, Patrick A; Widmer, Rolf; Williams, Ian D
2015-11-01
The mining of material resources requires knowledge about geogenic and anthropogenic deposits, in particular on the location of the deposits with the comparatively highest concentration of raw materials. In this study, we develop a framework that allows the establishment of analogies between geological and anthropogenic processes. These analogies were applied to three selected products containing rare earth elements (REE) in order to identify the most concentrated deposits in the anthropogenic cycle. The three identified anthropogenic deposits were characterised according to criteria such as "host rock", "REE mineralisation" and "age of mineralisation", i.e. regarding their "geological" setting. The results of this characterisation demonstrated that anthropogenic deposits have both a higher concentration of REE and a longer mine life than the evaluated geogenic deposit (Mount Weld, Australia). The results were further evaluated by comparison with the geological knowledge category of the United Nations Framework Classification for Fossil Energy and Mineral Reserves and Resources 2009 (UNFC-2009) to determine the confidence level in the deposit quantities. The application of our approach to the three selected cases shows a potential for recovery of REE in anthropogenic deposits; however, further exploration of both potential and limitations is required. Copyright © 2015 The Authors. Published by Elsevier Ltd.. All rights reserved.
Satellite data based approach for the estimation of anthropogenic heat flux over urban areas
NASA Astrophysics Data System (ADS)
Nitis, Theodoros; Tsegas, George; Moussiopoulos, Nicolas; Gounaridis, Dimitrios; Bliziotis, Dimitrios
2017-09-01
Anthropogenic effects in urban areas influence the thermal conditions in the environment and cause an increase of the atmospheric temperature. The cities are sources of heat and pollution, affecting the thermal structure of the atmosphere above them which results to the urban heat island effect. In order to analyze the urban heat island mechanism, it is important to estimate the anthropogenic heat flux which has a considerable impact on the urban energy budget. The anthropogenic heat flux is the result of man-made activities (i.e. traffic, industrial processes, heating/cooling) and thermal releases from the human body. Many studies have underlined the importance of the Anthropogenic Heat Flux to the calculation of the urban energy budget and subsequently, the estimation of mesoscale meteorological fields over urban areas. Therefore, spatially disaggregated anthropogenic heat flux data, at local and city scales, are of major importance for mesoscale meteorological models. The main objectives of the present work are to improve the quality of such data used as input for mesoscale meteorological models simulations and to enhance the application potential of GIS and remote sensing in the fields of climatology and meteorology. For this reason, the Urban Energy Budget concept is proposed as the foundation for an accurate determination of the anthropogenic heat discharge as a residual term in the surface energy balance. The methodology is applied to the cities of Athens and Paris using the Landsat ETM+ remote sensing data. The results will help to improve our knowledge on Anthropogenic Heat Flux, while the potential for further improvement of the methodology is also discussed.
NASA Astrophysics Data System (ADS)
Valdez Vasquez, M. C.; Chen, C. F.; Chiang, S. H.
2016-12-01
Forests in Honduras are one of the most important resources as they provide a wide range of environmental, economic, and social benefits. However, they are endangered as a result of the relentless occurrence of wildfires during the dry season. Despite the knowledge acquired by the population concerning the effects of wildfires, the frequency is increasing, a pattern attributable to the numerous ignition sources linked to human activity. The purpose of this study is to integrate the wildfire occurrences throughout the 2010-2015 period with a series of anthropogenic and non-anthropogenic variables using the random forest algorithm (RF). We use a series of variables that represent the anthropogenic activity, the flammability of vegetation, climatic conditions, and topography. To represent the anthropogenic activity, we included the continuous distances to rivers, roads, and settlements. To characterize the vegetation flammability, we used the normalized difference vegetation index (NDVI) and the normalized multi-band drought index (NMDI) acquired from MODIS surface reflectance data. Additionally, we included the topographical variables elevation, slope, and solar radiation derived from the ASTER global digital elevation model (GDEM V2). To represent the climatic conditions, we employed the land surface temperature (LST) product from the MODIS sensor and the WorldClim precipitation data. We analyzed the explanatory variables through native RF variable importance analysis and jackknife test, and the results revealed that the dry fuel conditions and low precipitation combined with the proximity to non-paved roads were the major drivers of wildfires. Furthermore, we predicted the areas with highest wildfire susceptibility, which are located mainly in the central and eastern regions of the country, within coniferous and mixed forests. Results acquired were validated using the area under the receiver operating characteristic (ROC) curve and the point biserial correlation and both validation metrics showed satisfactory agreement with the test data. Predictions of forest fire risk and its spatial variability are important instruments for proper management and the results acquired can lead to enhanced preventive measures to minimize risk and reduce the impacts caused by wildfires.
Nested-grid simulation of mercury over North America
NASA Astrophysics Data System (ADS)
Zhang, Y.; Jaeglé, L.; van Donkelaar, A.; Martin, R. V.; Holmes, C. D.; Amos, H. M.; Wang, Q.; Talbot, R.; Artz, R.; Brooks, S.; Luke, W.; Holsen, T. M.; Felton, D.; Miller, E. K.; Perry, K. D.; Schmeltz, D.; Steffen, A.; Tordon, R.; Weiss-Penzias, P.; Zsolway, R.
2012-01-01
We have developed a new high-resolution (1/2° latitude by 2/3° longitude) nested-grid mercury (Hg) simulation over North America employing the GEOS-Chem global chemical transport model. Emissions, chemistry, deposition, and meteorology are self-consistent between the global and nested domains. Compared to the global model (4° latitude by 5° longitude), the nested model shows improved skill at capturing the high spatial and temporal variability of Hg wet deposition over North America observed by the Mercury Deposition Network (MDN) in 2008-2009. The nested simulation resolves features such as land/ocean contrast and higher deposition due to orographic precipitation, and predicts more efficient convective rain scavenging of Hg over the southeast United States. However, the nested model overestimates Hg wet deposition over the Ohio River Valley region (ORV) by 27%. We modify anthropogenic emission speciation profiles in the US EPA National Emission Inventory (NEI) to account for the rapid in-plume reduction of reactive to elemental Hg (IPR simulation). This leads to a decrease in the model bias to +3% over the ORV region. Over the contiguous US, the correlation coefficient (r) between MDN observations and our IPR simulation increases from 0.63 to 0.78. The IPR nested simulation generally reproduces the seasonal cycle in surface concentrations of speciated Hg from the Atmospheric Mercury Network (AMNet) and Canadian Atmospheric Mercury Network (CAMNet). In the IPR simulation, annual mean reactive gaseous and particulate-bound Hg are within 80% and 10% of observations, respectively. In contrast, the simulation with unmodified anthropogenic Hg speciation profiles overestimates these observations by factors of 2 to 4. The nested model shows improved skill at capturing the horizontal variability of Hg observed over California during the ARCTAS aircraft campaign. We find that North American anthropogenic emissions account for 10-22% of Hg wet deposition flux over the US, depending on the anthropogenic emissions speciation profile assumed. The percent contribution can be as high as 60% near large point emission sources in ORV. The contribution for the dry deposition is 13-20%.
DOE Office of Scientific and Technical Information (OSTI.GOV)
Shaik, Aziz ur Rahman; Biswas, Haimanti, E-mail: haimanti.biswas@nio.org; Reddy, N.P.C.
In recent decades, material fluxes to coastal waters from various land based anthropogenic activities have significantly been enhanced around the globe which can considerably impact the coastal water quality and ecosystem health. Hence, there is a critical need to understand the links between anthropogenic activities in watersheds and its health. Kakinada Bay is situated at the SW part of the Bay of Bengal, near to the second largest mangrove cover in India with several fertilizer industries along its bank and could be highly vulnerable to different types of pollutants. However, virtually, no data is available so far reporting its physicochemicalmore » status and microalgal diversity at this bay. In order to fill this gap, we conducted three time series observations at a fixed station during January, December and June 2012, at this bay measuring more than 15 physical, chemical and biological parameters in every 3 h over a period of 36 h in both surface (0 m) and subsurface (4.5 m) waters. Our results clearly depict a strong seasonality between three sampling months; however, any abnormal values of nutrients, biological oxygen demand or dissolved oxygen level was not observed. A Skeletonema costatum bloom was observed in December which was probably influenced by low saline, high turbid and high Si input through the river discharge. Otherwise, smaller diatoms like Thalassiosira decipiens, Thalassiothrix frauenfeldii, and Thalassionema nitzschioides dominated the bay. It is likely that the material loading can be high at the point sources due to intense anthropogenic activities, however, gets diluted with biological, chemical and physical processes in the offshore waters. - Highlights: • No signature of enormous nutrient loading was observed over the diel cycle • Dissolved oxygen and BOD concentrations did not show any exceptional trend • Diatoms dominated more than 90% of the total phytoplankton communities • A Skeletonema Costatum (a centric diatom) bloom was noticed during December • No indication of pollution was noticed in terms of the parameters measured.« less
NASA Astrophysics Data System (ADS)
Hu, Ningjing; Liu, Jihua; Shi, Xuefa
2015-04-01
Source and distribution of sedimentary thallium in the Bohai Sea: Implications for hydrodynamic forces and anthropogenic impact Hu Ningjing, Liu Jihua, Shi Xuefa First Institute of Oceanography, State Oceanic Administration, Qingdao 266061, China Thallium (Tl), a non-essential and highly toxic trace metal, is listed as priority toxic pollutant by the United States Environmental Protection Agency (USEPA) (Keith and Telliard, 1979). However, its geochemical cycling in aquatic environment has received far less attention than that of many other trace metals. This has been attributed to relatively little commercial interest in Tl and, until recently, problems inherent in its detection at environmental concentrations (Meeravali and Jiang, 2008). In this study, we investigated the sources, distribution and fate of Tl in surface sediments of the Bohai Sea (BS), China, based on the datasets of total Tl and chemical speciation of Tl of 408 surface sediment samples in the total entire BS. The enrichment factors and chemical speciation of Tl indicated that Tl in BS was dominated by natural Tl, although anthropogenic Tl contamination was observed in the Liuguhe River mouth; the mud deposits are the sinks of Tl and the regional currents and tide systems play a key role on the accumulation of Tl in BS. The distribution of Tl consistent with that of MnO and Fe2O3 as well as the level of Fe-Mn fraction is relatively high, indicating MnO and Fe2O3 influence the geochemical behaviors of Tl in the BS. Although the positive correlation between Tl and TOC is observed for the samples in the BS, however, level of Tl in oxidizable faction could be neglected, suggesting TOC might not be a major factor affecting the concentration of Tl in BS. The low proportion of Tl in the non-residual fraction dominated by the Fe-Mn oxides suggested that the labile Tl was controlled by the Fe-Mn oxides and Tl has a low bioavailability and a minor potential threat to biota in BS. Acknowledgements: this work was jointly supported by National Natural Science Foundation of China (Grant Nos.41076032, 41276052 and 41376073) and the State Oceanic Administration, China (Grant No. 201105003). References Keith, L.H., Telliard, W.A., 1979. Priority pollutants-A perspective view. Environmental Science and Technology 13, 416-423. Meeravali, N.M., Jiang, S.-J., 2008. Ultra-trace speciation analysis of thallium in environmental water samples by inductively coupled plasma mass spectrometry after a novel sequential mixed-micelle cloud point extraction. Journal of Analytical Atomic Spectrometry 23, 555-560.
Elements and inorganic ions as source tracers in recent Greenland snow
NASA Astrophysics Data System (ADS)
Lai, Alexandra M.; Shafer, Martin M.; Dibb, Jack E.; Polashenski, Chris M.; Schauer, James J.
2017-09-01
Atmospheric transport of aerosols leads to deposition of impurities in snow, even in areas of the Arctic as remote as Greenland. Major ions (e.g. Na+, Ca2+, NH4+, K+, SO42-) are frequently used as tracers for common aerosol sources (e.g. sea spray, dust, biomass burning, anthropogenic emissions). Trace element data can supplement tracer ion data by providing additional information about sources. Although many studies have considered either trace elements or major ions, few have reported both. This study determined total and water-soluble concentrations of 31 elements (Al, As, Ca, Cd, Ce, Co, Cr, Dy, Eu, Fe, Gd, K, La, Mg, Mn, Na, Nb, Nd, Pb, Pr, S, Sb, Si, Sm, Sn, Sr, Ti, V, U, Y, Zn) in shallow snow pits at 22 sampling sites in Greenland, along a transect from Summit Station to sites in the northwest. Black carbon (BC) and inorganic ions were measured in colocated samples. Sodium, which is typically used as a tracer of sea spray, did not appear to have any non-marine sources. The rare earth elements, alkaline earth elements (Mg, Ca, Sr), and other crustal elements (Fe, Si, Ti, V) were not enriched above crustal abundances relative to Al, indicating that these elements are primarily dust sourced. Calculated ratios of non-sea salt Ca (nssCa) to estimated dust mass affirm the use of nssCa as a dust tracer, but suggest up to 50% uncertainty in that estimate in the absence of other crustal element data. Crustal enrichment factors indicated that As, Cd, Pb, non-sea-salt S, Sb, Sn, and Zn were enriched in these samples, likely by anthropogenic sources. Principal component analysis indicated more than one crustal factor, and a variety of factors related to anthropogenically enriched elements. Analysis of trace elements alongside major tracer ions does not change interpretation of ion-based source attribution for sources that are well-characterized by ions, but is valuable for assessing uncertainty in source attribution and identifying sources not represented by major ions.
NASA Astrophysics Data System (ADS)
Jongeward, A.; Li, Z.
2017-12-01
Aerosols from natural and anthropogenic sources can influence atmospheric variability and alter Earth's radiative balance through direct and indirect processes. Recently, policies targeting anthropogenic species (e.g. the Clean Air Act) have seen success in improving air quality. The anthropogenic contributions to the total aerosol loading and its spatiotemporal pattern/trend are anticipated to be altered. In this work the aerosol loading and trend over the North Atlantic Ocean since 2002 are examined, a period of significant change due to anthropogenic emissions control measures within the U.S. Monthly mean data from satellite (MODIS), ground (AERONET, IMPROVE), and model (GOCART, MERRA) sources are employed. Two annual trends in aerosol optical depth (AOD) observed by MODIS are present: a -0.020 decade-1 trend in the mid-latitudes and a 0.015 decade-1 trend in the sub-tropics. Trends in GOCART species AOD reveal anthropogenic (natural) species as the likely driver of the mid-latitude (sub-tropical) trend. AERONET AOD trends confirm negative AOD trends at three upwind sites in the Eastern U.S. and IMPROVE particulate matter (PM) observations identifies the role of decreasing ammonium sulfate in the overall PM decrease. Meanwhile, an increasing AOD trend seen during summertime in the eastern sub-tropics is associated with dust aerosol from North Africa. A dust parameterization from Kaufman et al. (2005) allows for changes in the flux transport across the sub-tropics to be calculated and analyzed. Using MERRA reanalysis fields, it is hypothesized that amplified warming and increases in baroclinic instability over the Saharan desert may lead to increased dust mobilization and export from North Africa to the sub-tropical Atlantic. This study provides updated analysis through 2016.
Heinen, De Carlo E.; Anthony, S.S.
2002-01-01
Trace metal concentrations in soils and in stream and estuarine sediments from a subtropical urban watershed in Hawaii are presented. The results are placed in the context of historical studies of environmental quality (water, soils, and sediment) in Hawaii to elucidate sources of trace elements and the processes responsible for their distribution. This work builds on earlier studies on sediments of Ala Wai Canal of urban Honolulu by examining spatial and temporal variations in the trace elements throughout the watershed. Natural processes and anthropogenic activity in urban Honolulu contribute to spatial and temporal variations of trace element concentrations throughout the watershed. Enrichment of trace elements in watershed soils result, in some cases, from contributions attributed to the weathering of volcanic rocks, as well as to a more variable anthropogenic input that reflects changes in land use in Honolulu. Varying concentrations of As, Cd, Cu, Pb and Zn in sediments reflect about 60 a of anthropogenic activity in Honolulu. Land use has a strong impact on the spatial distribution and abundance of selected trace elements in soils and stream sediments. As noted in continental US settings, the phasing out of Pb-alkyl fuel additives has decreased Pb inputs to recently deposited estuarine sediments. Yet, a substantial historical anthropogenic Pb inventory remains in soils of the watershed and erosion of surface soils continues to contribute to its enrichment in estuarine sediments. Concentrations of other elements (e.g., Cu, Zn, Cd), however, have not decreased with time, suggesting continued active inputs. Concentrations of Ba, Co, Cr, Ni, V and U, although elevated in some cases, typically reflect greater proportions attributed to natural sources rather than anthropogenic input. ?? 2002 Elsevier Science Ltd. All rights reserved.
Public water systems are increasingly facing higher bromide levels in their source waters from anthropogenic contamination through coal-fired power plants, conventional oil and gas extraction, and hydraulic fracturing. Climate change is likely to exacerbate this in coming years. ...
Public water systems are increasingly facing higher bromide levels in their source waters from anthropogenic contamination through coal-fired powerplants, conventional oil and gas extraction, and hydraulic fracturing. Climate change is likely to exacerbate this in coming years. W...
Source Apportionment of the Summer Time Carbonaceous Aerosol at Nordic Rural Background Sites
In the present study, natural and anthropogenic sources of particulate organic carbon (OCp) and elemental carbon (EC) have been quantified based on weekly filter samples of PM10 (particles with aerodynamic diameter <10µ collected at four Nordic rural backgro...
Urban surface waters can be impacted by anthropogenic sources such as impervious surfaces, sani-tary and storm sewers, and failing infrastructure. Fecal indicator bacteria (FIB) and microbial source tracking (MST) markers are common gauges of stream water qual-ity, however, litt...
Secondary organic aerosols (SOA), known to form in the atmosphere from oxidation of volatile organic compounds (VOCs) emitted by anthropogenic and biogenic sources, are a poorly understood but substantial component of atmospheric particles. In this study, we examined the chemic...
The Mercury Monitoring Workshop was developed because mercury contamination, both nationally and internationally, has long been recognized as a growing problem for both humans and ecosystems. Mercury is released to the environment from a variety of human (anthropogenic) sources i...
Anthropogenic emissions from a variety of sectors including mobile sources have decreased substantially over the past decades despite continued growth in population and economic activity. In this study, we analyze 1990-2010 trends in emission inventories, ambient observations and...
Tipping points in Anthropocene fluvial dynamics
NASA Astrophysics Data System (ADS)
Notebaert, Bastiaan; Broothaerts, Nils; Verstraeten, Gert; Berger, Jean-François; Houbrechts, Geoffrey
2016-04-01
Many rivers have undergone dramatic changes over the last millennia due to anthropogenic on- and offsite impacts. These changes have important implications for the geomorphic and hydrological functioning of the river. In this study we compare the influence of large-scaled off-site anthropogenic impact on three European river systems. We do this using traditional geomorphological methods, combined with palynological and archaeological data; for each catchment a Holocene sediment budget was constructed. The Dijle catchment is located in the central Belgian loess belt, and has undergone intense agriculture for at least the last 2000 year. Pre-Anthropocene floodplain are big marshes lacking a well-established river channel. Anthropogenic deforestation in the headwaters resulted in a sediment pulse from the Bronze Age on. In the main floodplain sediments gradually covered the peat layer, starting near a newly formed river channel and expanding over time towards the floodplain edges. In contrast, this transition is abrupt in the smaller tributary floodplains. Comparison with palynological data shows that this abrupt transition occurs when human impact reaches a certain threshold. The Valdaine region is located in the French Pre-Alps. Floodplain deposition increased over time since the Neolithic time period due to human induced and fire related soil erosion. This general aggradation trend is however interrupted by three major river incision phases which are caused by human land abandonment and dry periods. A second major change in floodplain geomorphology occurs during the High Roman Period and the last 800 year: the fine-grained meandering river changes to a gravel loaded braided river. During this period the upstream mountain reaches became a major sediment source due to deforestation, possibly combined with climate change. During the last century reforestation and land abandonment has led to a new incision phases, and floodplain are now a major source of gravel while the river partially maintains its braided pattern. The Amblève River in the Belgian Ardennes uplands underwent less dramatic changes. Large parts of the catchment are deforested during the last 700 years, leading to an increase in floodplain sedimentation. Despite this major sediment pulse, change in floodplain morphology remained limited to an increase in bank height. We argue that a combination of floodplain and channel morphology, the fine texture of supplied sediment and the high stream power of channel forming events result is a system that is less sensitive to change. Also the relative short time of impact may play a role. These three examples demonstrate the varying impact of human deforestation on floodplain geomorphology. For the Dijle and Valdaine region this lead to dramatic changes once a certain tipping point is reached. In contrast the Amblève river is more resilient to human impact due to its specific morphological setting. The morphology of the catchments and the nature of supplied sediments plays a major role in the sensitivity of fluvial systems to environmental impact. Once the tipping points are reached, it is difficult for the river to revert to its original state and floodplains remain highly impacted.
NASA Astrophysics Data System (ADS)
Bhati, S.; Mohan, M.
2016-12-01
Energy consumption in the urban environment impacts the urban surface energy budget and leads to the emission of anthropogenic sensible heat into the atmosphere. Anthropogenic heat (AH) can vary both in time and space, and are not readily measured. In present study, anthropogenic heat emissions have been estimated using an inventory approach for Delhi. The main sources that have been considered are electricity consumption, vehicular emissions, fuel consumption in domestic sector and waste heat from power plants. Total estimated anthropogenic heat is apportioned gridwise (2 km2) and incorporated in the WRF (version 3.5) model coupled with single-layer Urban canopy model (UCM) to assess the impact of these emissions on urban heat island effect in Delhi. Vehicular emissions have been found to be highest contributor to anthropogenic heat emissions (47%) followed by electricity consumption (28%), domestic fuel consumption (16%) and waste heat from power plants (9%). Highest annual average anthropogenic heat flux was estimated to be 25.2 Wm-2. High flux zones are observed in east Delhi and densely occupied and commercial zones of Sitaram Bazar and Connaught Place. Inclusion of anthropogenic heat emissions in the model improves model performance for near surface temperature as well as urban heat island intensities. Maximum simulated night-time UHI improves from 5.95°C (without AH) to 6.24°C (with AH) against observed value of 6.68°C, thereby indicating positive contribution of anthropogenic heat emissions along with urban canopy towards UHI effect in Delhi. Similarly, spatial distribution and UHI hotspots are found to be comparatively closer to corresponding observed distribution and hotspots with anthropogenic heat emissions being added to the WRF model. Overall, relatively improved model performance is indicative of the impact of anthropogenic heat emissions in local urban meteorology and urban heat island effect in Delhi. Hence, rising population and change in land use-cover and associated anthropogenic activities call for strategic mitigation measures in the city to prevent further strengthening of heat island effect.
Methods and Model Dependency of Extreme Event Attribution: The 2015 European Drought
NASA Astrophysics Data System (ADS)
Hauser, Mathias; Gudmundsson, Lukas; Orth, René; Jézéquel, Aglaé; Haustein, Karsten; Vautard, Robert; van Oldenborgh, Geert J.; Wilcox, Laura; Seneviratne, Sonia I.
2017-10-01
Science on the role of anthropogenic influence on extreme weather events, such as heatwaves or droughts, has evolved rapidly in the past years. The approach of "event attribution" compares the occurrence-probability of an event in the present, factual climate with its probability in a hypothetical, counterfactual climate without human-induced climate change. Several methods can be used for event attribution, based on climate model simulations and observations, and usually researchers only assess a subset of methods and data sources. Here, we explore the role of methodological choices for the attribution of the 2015 meteorological summer drought in Europe. We present contradicting conclusions on the relevance of human influence as a function of the chosen data source and event attribution methodology. Assessments using the maximum number of models and counterfactual climates with pre-industrial greenhouse gas concentrations point to an enhanced drought risk in Europe. However, other evaluations show contradictory evidence. These results highlight the need for a multi-model and multi-method framework in event attribution research, especially for events with a low signal-to-noise ratio and high model dependency such as regional droughts.
NASA Astrophysics Data System (ADS)
Hopcroft, Peter O.; Valdes, Paul J.; Kaplan, Jed O.
2018-04-01
The observed rise in atmospheric methane (CH4) from 375 ppbv during the Last Glacial Maximum (LGM: 21,000 years ago) to 680 ppbv during the late preindustrial era is not well understood. Atmospheric chemistry considerations implicate an increase in CH4 sources, but process-based estimates fail to reproduce the required amplitude. CH4 stable isotopes provide complementary information that can help constrain the underlying causes of the increase. We combine Earth System model simulations of the late preindustrial and LGM CH4 cycles, including process-based estimates of the isotopic discrimination of vegetation, in a box model of atmospheric CH4 and its isotopes. Using a Bayesian approach, we show how model-based constraints and ice core observations may be combined in a consistent probabilistic framework. The resultant posterior distributions point to a strong reduction in wetland and other biogenic CH4 emissions during the LGM, with a modest increase in the geological source, or potentially natural or anthropogenic fires, accounting for the observed enrichment of δ13CH4.
NASA Astrophysics Data System (ADS)
Nyberg, B.; Helland-Hansen, W.
2017-12-01
Long-term preservation of alluvial sediments is dependent on the hydrological processes that deposit sediments solely within an area that has available accomodation space and net subsidence know as a sedimentary basin. An understanding of the river processes contributing to terrestrial sedimentary basins is essential to fundamentally constrain and quantify controls on the modern terrestrial sink. Furthermore, the terrestrial source to sink controls place constraints on the entire coastal, shelf and deep marine sediment routing systems. In addition, the geographical importance of modern terrestrial sedimentary basins for agriculture and human settlements has resulted in significant upstream anthropogenic catchment modification for irrigation and energy needs. Yet to our knowledge, a global catchment model depicting the drainage patterns to modern terrestrial sedimentary basins has previously not been established that may be used to address these challenging issues. Here we present a new database of 180,737 global catchments that show the surface drainage patterns to modern terrestrial sedimentary basins. This is achieved by using high resolution river networks derived from digital elevation models in relation to newly acquired maps on global modern sedimentary basins to identify terrestrial sinks. The results show that active tectonic regimes are typically characterized by larger terrestrial sedimentary basins, numerous smaller source catchments and a high source to sink relief ratio. To the contrary passive margins drain catchments to smaller terrestrial sedimentary basins, are composed of fewer source catchments that are relatively larger and a lower source to sink relief ratio. The different geomorphological characteristics of source catchments by tectonic setting influence the spatial and temporal patterns of fluvial architecture within sedimentary basins and the anthropogenic methods of exploiting those rivers. The new digital database resource is aimed to help the geoscientific community to contribute further to our quantitative understanding of source-to-sink systems and its allogenic and autogenic controls, geomorphological characteristics, terrestrial sediment transit times and the anthropogenic impact on those systems.
Hu, Qihou; Xie, Zhouqing; Wang, Xinming; Kang, Hui; Zhang, Yuqing; Ding, Xiang; Zhang, Pengfei
2018-05-30
Organic acids are major components in marine organic aerosols. Many studies on the occurrence, sources and sinks of organic acids over oceans in the low and middle latitudes have been conducted. However, the understanding of relative contributions of specific sources to organic acids over oceans, especially in the high latitudes, is still inadequate. This study measured organic acids, including C 14:0 - C 32:0 saturated monocarboxylic acids (MCAs), C 16:1 , C 18:1 and C 18:2 unsaturated MCAs, and di-C 4 - di-C 10 dicarboxylic acids (DCAs), in the marine boundary layer from the East China Sea to the Arctic Ocean during the 3rd Chinese Arctic Research Expedition (CHINARE 08). The average concentrations were 18 ± 16 ng/m 3 and 11 ± 5.4 ng/m 3 for ΣMCA and ΣDCA, respectively. The levels of saturated MCAs were much higher than those of unsaturated DCAs, with peaks at C 16:0 , C 18:0 and C 14:0 . DCAs peaked at di-C 4 , followed by di-C 9 and di-C 8 . Concentrations of MCAs and DCAs generally decreased with increasing latitudes. Sources of MCAs and DCAs were further investigated using principal component analysis with a multiple linear regression (PCA-MLR) model. Overall, carboxylic acids originated from ocean emissions, continental input (including biomass burning, anthropogenic emissions and terrestrial plant emissions), and secondary formation. All the five sources contributed to MCAs with ocean emissions as the predominant source (48%), followed by biomass burning (20%). In contrast, only 3 sources (i.e., secondary formation (50%), anthropogenic emissions (41%) and biomass burning (9%)) contributed to DCAs. Furthermore, the sources varied with regions. Over the Arctic Ocean, only secondary formation and anthropogenic emissions contributed to MCAs and DCAs. Copyright © 2018 Elsevier B.V. All rights reserved.
A radiogenic isotope tracer study of transatlantic dust transport from Africa to the Caribbean
NASA Astrophysics Data System (ADS)
Kumar, A.; Abouchami, W.; Galer, S. J. G.; Garrison, V. H.; Williams, E.; Andreae, M. O.
2014-01-01
Many studies have suggested that long-range transport of African desert dusts across the Atlantic Ocean occurs, delivering key nutrients and contributing to fertilization of the Amazon rainforest. Here we utilize radiogenic isotope tracers - Sr, Nd and Pb - to derive the provenance, local or remote, and pathways of dust transport from Africa to the Caribbean. Atmospheric total suspended particulate (TSP) matter was collected in 2008 on quartz fibre filters, from both sides of the Atlantic Ocean at three different locations: in Mali (12.6°N, 8.0°W; 555 m a.s.l.), Tobago (11.3°N, 60.5°W; 329 m a.s.l.) and the U.S. Virgin Islands (17.7°N, 64.6°W; 27 m a.s.l.). Both the labile phase, representative of the anthropogenic signal, and the refractory detrital silicate fraction were analysed. Dust deposits and soils from around the sampling sites were measured as well to assess the potential contribution from local sources to the mineral dust collected. The contribution from anthropogenic sources of Pb was predominant in the labile, leachate phase. The overall similarity in Pb isotope signatures found in the leachates is attributed to a common African source of anthropogenic Pb, with minor inputs from other sources, such as from Central and South America. The Pb, Sr and Nd isotopic compositions in the silicate fraction were found to be systematically more radiogenic than those in the corresponding labile phases. In contrast, Nd and Sr isotopic compositions from Mali, Tobago, and the Virgin Islands are virtually identical in both leachates and residues. Comparison with existing literature data on Saharan and Sahelian sources constrains the origin of summer dust transported to the Caribbean to mainly originate from the Sahel region, with some contribution from northern Saharan sources. The source regions derived from the isotope data are consistent with 7-day back-trajectory analyses, demonstrating the usefulness of radiogenic isotopes in tracing dust provenance and atmospheric transport.
Xu, Yonghang; Sun, Qinqin; Ye, Xiang; Yin, Xijie; Li, Dongyi; Wang, Liang; Wang, Aijun; Li, Yunhai
2017-05-01
The geochemical compositions of sediments in the Dongshan Bay, a semi-enclosed bay on the southeast coast of China, were obtained to identify pollutant sources and evaluate the anthropogenic impacts over the last 100 years. The results indicated that the metal flux had been increasing since the 1980s. Enrichment factor values (Pb, Zn and Cu) suggested only slight enrichment. The proportion of anthropogenic Pb changed from 9% to 15% during 2000-2014. Coal combustion might be an important contamination source in the Dongshan Bay. The historical variation in the metal flux reflected the economic development and urbanization in the Zhangjiang drainage area in the past 30 years. According to the Landsat satellite remote sensing data, the urbanization area expanded approximately three times from 1995 to 2010. The δ 13 C values (-21‰ to -23‰) of the organic matter (OM) in the sediments indicated that the OM was primarily sourced from aquatic, terrigenous and marsh C 3 plants. Nitrogen was mainly derived from aquatic plants and terrigenous erosion before the 1980s. However, the total organic carbon (TOC) contents, total nitrogen (TN) contents and δ 15 N had been increasing since the 1980s, which suggested that the sources of nitrogen were soil erosion, fertilizer and sewage. In addition, the TOC and TN fluxes in the Dongshan Bay had significantly increased since the 1980s, which reflected the use of N fertilizer. However, the TOC and TN fluxes significantly decreased in the past decade because environmental awareness increased and environmental protection policies were implemented. Copyright © 2017 Elsevier Ltd. All rights reserved.
Hu, Yuanan; Liu, Xueping; Bai, Jinmei; Shih, Kaimin; Zeng, Eddy Y; Cheng, Hefa
2013-09-01
Heavy metals in the surface soils from lands of six different use types in one of the world's most densely populated regions, which is also a major global manufacturing base, were analyzed to assess the impact of urbanization and industrialization on soil pollution. A total of 227 surface soil samples were collected and analyzed for major heavy metals (As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, and Zn) by using microwave-assisted acid digestion and inductively coupled plasma-mass spectrometry (ICP-MS). Multivariate analysis combined with enrichment factors showed that surface soils from the region (>7.2 × 10(4) km(2)) had mean Cd, Cu, Zn, and As concentrations that were over two times higher than the background values, with Cd, Cu, and Zn clearly contributed by anthropogenic sources. Soil pollution by Pb was more widespread than the other heavy metals, which was contributed mostly by anthropogenic sources. The results also indicate that Mn, Co, Fe, Cr, and Ni in the surface soils were primarily derived from lithogenic sources, while Hg and As contents in the surface soils were controlled by both natural and anthropogenic sources. The pollution level and potential ecological risk of the surface soils both decreased in the order of: urban areas > waste disposal/treatment sites ∼ industrial areas > agricultural lands ∼ forest lands > water source protection areas. These results indicate the significant need for the development of pollution prevention and reduction strategies to reduce heavy metal pollution for regions undergoing fast industrialization and urbanization.
NASA Astrophysics Data System (ADS)
Skorokhod, Andrey; Belikov, Igor; Shtabkin, Yury; Moiseenko, Konstantin; Pankratova, Natalia; Vasileva, Anastasia; Rakitin, Vadim; Heimann, Martin
2015-04-01
Direct observations of atmospheric air composition are very important for a comprehensive understanding of atmospheric chemistry over Northern Eurasia and its variability and trends driven by abrupt climatic and ecosystem changes and anthropogenic pressure. Atmospheric air composition (including greenhouse gases and aerosols), its trends and variability is still insufficiently known for most of the nearly uninhabited areas of Northern Eurasia. This limits the accuracy of both global and regional models, which simulate climatological and ecosystem changes in this highly important region. From that point of view, the Zotino Tall Tower Observatory (ZOTTO) in the middle of Siberia (near 60N, 90E), launched in 2006 and governed by a scientific international consortium plays an important role providing unique information about concentrations of greenhouse and reactive trace gases, as well as aerosols. Simulations of surface concentrations of O3, NOx and CO performed by global chemical-transport model GEOS-Chem using up-to-date anthropogenic and biogenic emissions databases show very good agreement with values observed at ZOTTO in 2007-2012. Observed concentration of ozone has a pronounced seasonal variation with a clear peak in spring (40-45 ppbv in average and up to 80 ppbv in extreme cases) and minimum in winter. Average ozone level is about 20 ppbv that corresponds to the background conditions. Enhanced concentration in March-July is due to increased stratospheric-tropospheric exchange. In autumn and winter distribution of ozone is close to uniform. NOx concentration does not exceed 1 ppb that is typical for background areas but may vary by order and some more in few hours. Higher surface NOx(=NO+NO2) concentrations during day time generally correspond to higher ozone when NO/NO2 ratio indicates on clean or slightly polluted conditions. CO surface concentration has a vivid seasonal course and varies from about 100 ppb in summer till 150 ppb in winter. But during polluted cases which are quite regular CO may increase till 400 ppb and more. Most uncertainties are due to the wild fires, which are often in different regions of Siberia. Numerical assessment of climatically important natural and anthropogenic emission sources influencing observed CO and O3 concentrations and their seasonal variability was made using GEOS-Chem model. According to the results, during the cold period CO concentrations in the surface layer is largely driven atmospheric transport from anthropogenic sources in Western Europe (up to 20 ppb), south of European Russia (up to 35 ppb) and south-western Siberia (up to 28 ppb). During the warm season they are usually affected by air transport from eastern Siberia, where the main contribution to the CO emissions are biogenic VOC oxidation (up to 15 ppb) and wildfires (up to 12 ppb). Transport of pollutants from south-western Siberia can add about 2,5 ppb to the ozone summer level in Central Siberia. In wintertime this factor leads to a reduced surface ozone level by 2 ppb. The contribution of large remote emission sources (Europe) is estimated within 1 ppb. Generally the simulation results indicate a significant role of long-range air transport in addition to regional natural and anthropogenic sources of air pollution which determine the total balance of surface CO. These processes need to be considered in quantitative analyses of the factors that determine the long-term photochemical system evolution in the lower troposphere over the continental regions of Northern Eurasia. This work was supported by the Russian Scientific Fund under grant 14-47-00049.
NASA Astrophysics Data System (ADS)
Chen, J.; Gaillardet, J.; Louvat, P.; Birck, J.
2009-05-01
Metal contamination is a major issue of human impact on the aqueous environment. River water is particularly susceptible to contamination for both dissolved and particulate loads, displaying a major challenge in understanding the dominant sources and pathways of metals in polluted drainage basins. Recent improvements in mass spectrometry allow isotopic measurements of "non-traditional" metals (Zn, Cu, Fe, etc.), making their isotopes a new potential device to investigate contamination of metals under dissolved and particulate forms in rivers. We focus here on Zn isotope geochemistry in the largely anthropized Seine River (France). A new protocol of two-column separation of Zn from dilute aqueous solution has been developed and proven to be reproducible and satisfactory for accurate measurement of Zn isotopic ratios in water samples by MC-ICP-MS (2σ = 0.04‰). Preliminary results show a total variation of 0.65‰ for δ66Zn in dissolved phases of the Seine basin, and a light isotope enrichment in anthropogenic sources compared to other water samples. The determined conservative behavior of Zn in river water makes its isotopes an effective probe of anthropogenic contamination. The natural and anthropogenic inputs were clearly identified and calculated based on Zn isotope compositions for dissolved loads. Suspended particular matters (SPM) display different Zn isotope compositions compared to dissolved loads, with a total δ66Zn variation of 0.22‰. Zn concentrations and its isotope compositions in SPM reveal inverse relationships as function of the distance from the headwater and the SPM content for geographical and temporal samples, respectively. The δ66Zn data in SPM are interpreted as reflecting the mixture of natural and anthropogenic particles. The correlation between dissolved and particulate δ66Zn shows that adsorption processes are not the dominant process making Zn enrichment in SPM. We report here for the first time systematic δ66Zn data in waters of a whole river basin, showing Zn isotopes a powerful probe to trace contamination sources and biogeochemical processes in hydrologic systems.
NASA Astrophysics Data System (ADS)
Abou Rafee, Sameh A.; Martins, Leila D.; Kawashima, Ana B.; Almeida, Daniela S.; Morais, Marcos V. B.; Souza, Rita V. A.; Oliveira, Maria B. L.; Souza, Rodrigo A. F.; Medeiros, Adan S. S.; Urbina, Viviana; Freitas, Edmilson D.; Martin, Scot T.; Martins, Jorge A.
2017-06-01
This paper evaluates the contributions of the emissions from mobile, stationary and biogenic sources on air pollution in the Amazon rainforest by using the Weather Research and Forecasting with Chemistry (WRF-Chem) model. The analyzed air pollutants were CO, NOx, SO2, O3, PM2. 5, PM10 and volatile organic compounds (VOCs). Five scenarios were defined in order to evaluate the emissions by biogenic, mobile and stationary sources, as well as a future scenario to assess the potential air quality impact of doubled anthropogenic emissions. The stationary sources explain the highest concentrations for all air pollutants evaluated, except for CO, for which the mobile sources are predominant. The anthropogenic sources considered resulted an increasing in the spatial peak-temporal average concentrations of pollutants in 3 to 2780 times in relation to those with only biogenic sources. The future scenario showed an increase in the range of 3 to 62 % in average concentrations and 45 to 109 % in peak concentrations depending on the pollutant. In addition, the spatial distributions of the scenarios has shown that the air pollution plume from the city of Manaus is predominantly transported west and southwest, and it can reach hundreds of kilometers in length.
Constraining wintertime sources of inorganic chlorine over the northeast United States
NASA Astrophysics Data System (ADS)
Haskins, J.; Jaegle, L.; Shah, V.; Lopez-Hilfiker, F.; Lee, B. H.; Campuzano Jost, P.; Schroder, J. C.; Day, D. A.; Fiddler, M. N.; Holloway, J. S.; Sullivan, A.; Veres, P. R.; Weber, R. J.; Dibb, J. E.; Brown, S. S.; Jimenez, J. L.; Thornton, J. A.
2017-12-01
Wintertime multiphase chlorine chemistry is thought to play a significant role in the regional distribution of oxidants, the lifetime of VOCs, and the transport of NOx downwind of urban sources. However, the sources and chemistry of reactive chlorine remain highly uncertain. During the WINTER 2015 aircraft campaign, the inorganic chlorine budget was dominated by HCl (g) and total particulate chloride, accounting for greater than 85% of the total chlorine budget within the boundary layer. The total concentration of inorganic chlorine compounds found over marine regions was 1014 pptv and 609 pptv over continental regions with variability found to be driven by changes in meteorological conditions, particle liquid water content, particle pH, and proximity to large anthropogenic sources. However, displacement of particle chloride was often not a large enough source to fully explain the concentrations of gas phase Cly compounds. We use the GEOS-Chem global chemical transport model to simulate the emissions, gas-particle partitioning, and downwind transport and deposition of Cly during winter. Simulated concentrations of HCl, particle chloride, and other dominant Cly compounds are compared to measurements made during the WINTER aircraft campaign. The relative roles of Cly sources from sea-salt aerosol and anthropogenic sources such as power plants, biomass burning and road salt are explored.
Brunker, K; Hampson, K; Horton, D L; Biek, R
2012-12-01
Landscape epidemiology and landscape genetics combine advances in molecular techniques, spatial analyses and epidemiological models to generate a more real-world understanding of infectious disease dynamics and provide powerful new tools for the study of RNA viruses. Using dog rabies as a model we have identified how key questions regarding viral spread and persistence can be addressed using a combination of these techniques. In contrast to wildlife rabies, investigations into the landscape epidemiology of domestic dog rabies requires more detailed assessment of the role of humans in disease spread, including the incorporation of anthropogenic landscape features, human movements and socio-cultural factors into spatial models. In particular, identifying and quantifying the influence of anthropogenic features on pathogen spread and measuring the permeability of dispersal barriers are important considerations for planning control strategies, and may differ according to cultural, social and geographical variation across countries or continents. Challenges for dog rabies research include the development of metapopulation models and transmission networks using genetic information to uncover potential source/sink dynamics and identify the main routes of viral dissemination. Information generated from a landscape genetics approach will facilitate spatially strategic control programmes that accommodate for heterogeneities in the landscape and therefore utilise resources in the most cost-effective way. This can include the efficient placement of vaccine barriers, surveillance points and adaptive management for large-scale control programmes.
Dynamic Stocks and Flows Analysis of Bisphenol A (BPA) in China: 2000-2014.
Jiang, Daqian; Chen, Wei-Qiang; Zeng, Xianlai; Tang, Linbin
2018-03-20
Bisphenol A (BPA), a synthetic organic chemical, is creating a new category of ecological and human health challenges due to unintended leakage. Effectively managing the use and leakage of BPA can benefit from an understanding of the anthropogenic BPA cycles (i.e., the size of BPA flows and stocks). In this work, we provide a dynamic analysis of the anthropogenic BPA cycles in China for 2000-2014. We find that China's BPA consumption has increased 10-fold since 2000, to ∼3 million tonnes/year. With the increasing consumption, China's in-use BPA stock has increased 500-fold to 14.0 million tonnes (i.e., 10.2 kg BPA/capita). It is unclear whether a saturation point has been reached, but in 2004-2014, China's in-use BPA stock has been increasing by 0.8 kg BPA/capita annually. Electronic products are the biggest contributor, responsible for roughly one-third of China's in-use BPA stock. Optical media (DVD/VCD/CDs) is the largest contributor to China's current End-of-Life (EoL) BPA flow, totaling 0.9 million tonnes/year. However, the EoL BPA flow due to e-waste will increase quickly, and will soon become the largest EoL BPA flow. The changing quantities and sources of EoL BPA flows may require a shift in the macroscopic BPA management strategies.
Tropospheric ozone in the Nisqually River Drainage, Mount Rainier National Park
Peterson, D.L.; Bowers, Darci
1999-01-01
We quantified the summertime distribution of tropospheric ozone in the topographically complex Nisqually River drainage of Mount Rainier National Park from 1994 to 1997. Passive ozone samplers were used along an elevational transect to measure weekly average ozone concentrations ranging from 570 m to 2040 m elevation. Weekly average ozone concentrations were positively correlated with elevation, with the highest concentrations consistently measured at the highest sampling site (Panorama Point). Weekly average ozone concentrations at Mount Rainier National Park are considerably higher than those in the Seattle-Tacoma metropolitan area to the west. The anthropogenic contribution to ozone within the Nisqually drainage was evaluated by comparing measurements at this location with measurements from a 'reference' site in the western Olympic Mountains. The comparison suggests there is a significant anthropogenic source of ozone reaching the Cascade Range via atmospheric transport from urban areas to the west. In addition. temporal (week to week) variation in ozone distribution is synchronous within the Nisqually drainage, which indicates that subregional patterns are detectable with weekly averages. The Nisqually drainage is likely the 'hot spot' for air pollution in Mount Rainier National Park. By using passive ozone samplers in this drainage in conjunction with a limited number of continuous analyzers, the park will have a robust monitoring approach for measuring tropospheric ozone over time and protecting vegetative and human health.
NASA Astrophysics Data System (ADS)
Debevec, Cécile; Sauvage, Stéphane; Gros, Valérie; Sciare, Jean; Pikridas, Michael; Stavroulas, Iasonas; Salameh, Thérèse; Leonardis, Thierry; Gaudion, Vincent; Depelchin, Laurence; Fronval, Isabelle; Sarda-Esteve, Roland; Baisnée, Dominique; Bonsang, Bernard; Savvides, Chrysanthos; Vrekoussis, Mihalis; Locoge, Nadine
2017-09-01
More than 7000 atmospheric measurements of over 60 C2 - C16 volatile organic compounds (VOCs) were conducted at a background site in Cyprus during a 1-month intensive field campaign held in March 2015. This exhaustive dataset consisted of primary anthropogenic and biogenic VOCs, including a wide range of source-specific tracers, and oxygenated VOCs (with various origins) that were measured online by flame ionization detection-gas chromatography and proton transfer mass spectrometry. Online submicron aerosol chemical composition was performed in parallel using an aerosol mass spectrometer. This study presents the high temporal variability in VOCs and their associated sources. A preliminary analysis of their time series was performed on the basis of independent tracers (NO, CO, black carbon), meteorological data and the clustering of air mass trajectories. Biogenic compounds were mainly attributed to a local origin and showed compound-specific diurnal cycles such as a daily maximum for isoprene and a nighttime maximum for monoterpenes. Anthropogenic VOCs as well as oxygenated VOCs displayed higher mixing ratios under the influence of continental air masses (i.e., western Asia), indicating that long-range transport significantly contributed to the VOC levels in the area. Source apportionment was then conducted on a database of 20 VOCs (or grouped VOCs) using a source receptor model. The positive matrix factorization and concentration field analyses were hence conducted to identify and characterize covariation factors of VOCs that were representative of primary emissions as well as chemical transformation processes. A six-factor PMF solution was selected, namely two primary biogenic factors (relative contribution of 43 % to the total mass of VOCs) for different types of emitting vegetation; three anthropogenic factors (short-lived combustion source, evaporative sources, industrial and evaporative sources; 21 % all together), identified as being either of local origin or from more distant emission zones (i.e., the south coast of Turkey); and a last factor (36 %) associated with regional background pollution (air masses transported both from the Western and Eastern Mediterranean regions). One of the two biogenic and the regional background factors were found to be the largest contributors to the VOC concentrations observed at our sampling site. Finally, a combined analysis of VOC PMF factors with source-apportioned organic aerosols (OAs) helped to better distinguish between anthropogenic and biogenic influences on the aerosol and gas phase compositions. The highest OA concentrations were observed when the site was influenced by air masses rich in semi-volatile OA (less oxidized aerosols) originating from the southwest of Asia, in contrast with OA factor contributions associated with the remaining source regions. A reinforcement of secondary OA formation also occurred due to the intense oxidation of biogenic precursors.
de Carvalho-Souza, Gustavo Freire; de A Miranda, Daniele; Pataro, Luciano
2016-04-15
Marine species are experiencing unprecedented global impacts due to anthropogenic debris. Many recent studies have pointed out the hazards associated with marine litter ingestion, especially plastic debris - the most abundant and ubiquitous items in coastal and oceanic environments worldwide. In this study we provide the first in situ evidence of consumption of non-discarded synthetic rope fragments by green turtles. We explored the environmental risks to this endangered species associated with the grazing and consumption of anthropogenic debris in zones of human activity. Efforts to combat debris ingestion and reduce anthropogenic debris discharged into the world's oceans should be a priority for decision-makers and will need to involve multiple-approaches and the adoption of more environmentally friendly products and practices by the international community. Copyright © 2016 Elsevier Ltd. All rights reserved.
NASA Astrophysics Data System (ADS)
Mei, Linlu; Xue, Yong
2013-04-01
The Arctic atmosphere is perturbed by nature/anthropogenic aerosol sources known as the Arctic haze, was firstly observed in 1956 by J. Murray Mitchell in Alaska (Mitchell, 1956). Pacyna and Shaw (1992) summarized that Arctic haze is a mixture of anthropogenic and natural pollutants from a variety of sources in different geographical areas at altitudes from 2 to 4 or 5 km while the source for layers of polluted air at altitudes below 2.5 km mainly comes from episodic transportation of anthropogenic sources situated closer to the Arctic. Arctic haze of low troposphere was found to be of a very strong seasonal variation characterized by a summer minimum and a winter maximum in Alaskan (Barrie, 1986; Shaw, 1995) and other Arctic region (Xie and Hopke, 1999). An anthropogenic factor dominated by together with metallic species like Pb, Zn, V, As, Sb, In, etc. and nature source such as sea salt factor consisting mainly of Cl, Na, and K (Xie and Hopke, 1999), dust containing Fe, Al and so on (Rahn et al.,1977). Black carbon and soot can also be included during summer time because of the mix of smoke from wildfires. The Arctic air mass is a unique meteorological feature of the troposphere characterized by sub-zero temperatures, little precipitation, stable stratification that prevents strong vertical mixing and low levels of solar radiations (Barrie, 1986), causing less pollutants was scavenged, the major revival pathway for particulates from the atmosphere in Arctic (Shaw, 1981, 1995; Heintzenberg and Larssen, 1983). Due to the special meteorological condition mentioned above, we can conclude that Eurasian is the main contributor of the Arctic pollutants and the strong transport into the Arctic from Eurasia during winter caused by the high pressure of the climatologically persistent Siberian high pressure region (Barrie, 1986). The paper intends to address the atmospheric characteristics of Arctic haze by comparing the clear day and haze day using different dataset, including satellite remote sensing, ground-based observations and modelling. The key question is which information should be used for analysis and how to integrate the source information. The behavior of different atmospheric parameters as described in the paper is consistent and the analysis using satellite atmospheric parameters is in line with synoptic charts. Hence the different data sources are complementary and the results support each other (Mei et al., 2011). In the paper, Aerosol Optical Depth (AOD) from both satellite retrieval data and ground-based measurements were analyzed the characteristic, especially the absorption. We also discuss the effect of Arctic haze to the Arctic temperature, snow albedo and arctic flux in details.
Environmental conditions influence tissue regeneration rates in scleractinian corals.
Sabine, Alexis M; Smith, Tyler B; Williams, Dana E; Brandt, Marilyn E
2015-06-15
Natural and anthropogenic factors may influence corals' ability to recover from partial mortality. To examine how environmental conditions affect lesion healing, we assessed several water quality parameters and tissue regeneration rates in corals at six reefs around St. Thomas, US Virgin Islands. We hypothesized that sites closer to developed areas would have poor water quality due to proximity to anthropogenic stresses, which would impede tissue regeneration. We found that water flow and turbidity most strongly influenced lesion recovery rates. The most impacted site, with high turbidity and low flow, recovered almost three times slower than the least impacted site, with low turbidity, high flow, and low levels of anthropogenic disturbance. Our results illustrate that in addition to lesion-specific factors known to affect tissue regeneration, environmental conditions can also control corals' healing rates. Resource managers can use this information to protect low-flow, turbid nearshore reefs by minimizing sources of anthropogenic stress. Copyright © 2015 Elsevier Ltd. All rights reserved.
The importance of invertebrates when considering the impacts of anthropogenic noise
Morley, Erica L.; Jones, Gareth; Radford, Andrew N.
2014-01-01
Anthropogenic noise is now recognized as a major global pollutant. Rapidly burgeoning research has identified impacts on individual behaviour and physiology through to community disruption. To date, however, there has been an almost exclusive focus on vertebrates. Not only does their central role in food webs and in fulfilling ecosystem services make imperative our understanding of how invertebrates are impacted by all aspects of environmental change, but also many of their inherent characteristics provide opportunities to overcome common issues with the current anthropogenic noise literature. Here, we begin by explaining why invertebrates are likely to be affected by anthropogenic noise, briefly reviewing their capacity for hearing and providing evidence that they are capable of evolutionary adaptation and behavioural plasticity in response to natural noise sources. We then discuss the importance of quantifying accurately and fully both auditory ability and noise content, emphasizing considerations of direct relevance to how invertebrates detect sounds. We showcase how studying invertebrates can help with the behavioural bias in the literature, the difficulties in drawing strong, ecologically valid conclusions and the need for studies on fitness impacts. Finally, we suggest avenues of future research using invertebrates that would advance our understanding of the impact of anthropogenic noise. PMID:24335986
The importance of invertebrates when considering the impacts of anthropogenic noise.
Morley, Erica L; Jones, Gareth; Radford, Andrew N
2014-02-07
Anthropogenic noise is now recognized as a major global pollutant. Rapidly burgeoning research has identified impacts on individual behaviour and physiology through to community disruption. To date, however, there has been an almost exclusive focus on vertebrates. Not only does their central role in food webs and in fulfilling ecosystem services make imperative our understanding of how invertebrates are impacted by all aspects of environmental change, but also many of their inherent characteristics provide opportunities to overcome common issues with the current anthropogenic noise literature. Here, we begin by explaining why invertebrates are likely to be affected by anthropogenic noise, briefly reviewing their capacity for hearing and providing evidence that they are capable of evolutionary adaptation and behavioural plasticity in response to natural noise sources. We then discuss the importance of quantifying accurately and fully both auditory ability and noise content, emphasizing considerations of direct relevance to how invertebrates detect sounds. We showcase how studying invertebrates can help with the behavioural bias in the literature, the difficulties in drawing strong, ecologically valid conclusions and the need for studies on fitness impacts. Finally, we suggest avenues of future research using invertebrates that would advance our understanding of the impact of anthropogenic noise.
Lagrangian modeling of global atmospheric methane (1990-2012)
NASA Astrophysics Data System (ADS)
Arfeuille, Florian; Henne, Stephan; Brunner, Dominik
2016-04-01
In the MAIOLICA-II project, the lagrangian particle model FLEXPART is used to simulate the global atmospheric methane over the 1990-2012 period. In this lagrangian framework, 3 million particles are permanently transported based on winds from ERA-interim. The history of individual particles can be followed allowing for a comprehensive analysis of transport pathways and timescales. The link between sources (emissions) and receptors (measurement stations) is then established in a straightforward manner, a prerequisite for source inversion problems. FLEXPART was extended to incorporate the methane loss by reaction with OH, soil uptake and stratospheric loss reactions with prescribed Cl and O(1d) radicals. Sources are separated into 245 different tracers, depending on source origin (anthropogenic, wetlands, rice, biomass burning, termites, wild animals, oceans, volcanoes), region of emission, and time since emission (5 age classes). The inversion method applied is a fixed-lag Kalman smoother similar to that described in Bruhwiler et al. [2005]. Results from the FLEXPART global methane simulation and from the subsequent inversion will be presented. Results notably suggest: - A reduction in methane growth rates due to diminished wetland emissions and anthropogenic European emission in 1990-1993. - A second decrease in 1995-1996 is also mainly attributed to these two emission categories. - A reduced increase in Chinese anthropogenic emissions after 2003 compared to EDGAR inventories. - Large South American wetlands emissions during the entire period. Bruhwiler, L. M. P., Michalak, A. M., Peters, W., Baker, D. F. & Tans, P. 2005: An improved Kalman smoother fore atmospheric inversions, Atmos Chem Phys, 5, 2691-2702.
Precipitation chemistry over urban, rural and high altitude Himalayan stations in eastern India
NASA Astrophysics Data System (ADS)
Roy, Arindam; Chatterjee, Abhijit; Tiwari, Suresh; Sarkar, Chirantan; Das, Sanat Kumar; Ghosh, Sanjay Kumar; Raha, Sibaji
2016-11-01
A study of precipitation (rainwater) chemistry during the two consecutive summer monsoon seasons of 2013 and 2014 at a high altitude station (2200 m asl) at eastern Himalaya region (Darjeeling); a typical metropolitan urban location (Kolkata), and a rural environment near the Bay of Bengal (Falta) was conducted. The volume-weighted mean (VWM) concentration shows that total ionic composition was maximum over Kolkata (391 μeq l- 1) followed by Falta (204 μeq l- 1) and Darjeeling (64 μeq l- 1). 85% rain samples were alkaline over Kolkata, whereas, 55 and 65% samples were acidic over Falta and Darjeeling respectively. Ca2 + was the most potential species to completely neutralize the acidity over Kolkata, whereas, NH4+ was the potential species to partially neutralize the acidity over Falta and Darjeeling. The deposition fluxes of anthropogenic and dust species over Kolkata was remarkably higher than Falta and Darjeeling. Anthropogenic and dust chemical species in rainwater were found to be dominant over Kolkata and Falta when the air masses passes from the polluted continental region. Rainwater acidity over Darjeeling was highest when air masses arrived from the Arabian Sea compared to air masses from the Bay of Bengal. Positive matrix factorization model was used for the source apportionment of the ionic species scavenged by rain. Comparable contributions of marine, dust, and anthropogenic sources were identified as major source over Kolkata. The major contributions were identified from marine and fossil fuel burning over Falta, whereas, marine, biomass/coal burning, ammonia from agricultural activities and domestic wastes were identified as the major sources over Darjeeling.
Soluble dust as source of nutrients to the oceans and the role of humans
NASA Astrophysics Data System (ADS)
Tsigaridis, K.; Kanakidou, M.; Myriokefalitakis, S.; Nikolaou, P.; Daskalakis, N.; Theodosi, C.; Nenes, A.; Mihalopoulos, N.
2014-12-01
Atmospheric deposition of trace constituents, both of natural and anthropogenic origin, can act as a nutrient source into the open ocean and affect marine ecosystem functioning and subsequently the exchange of CO2 between the atmosphere and the global ocean. Dust is known as a major source of nutrients (Fe and P) into the atmosphere, but only a fraction of these nutrients is released in soluble form that can be assimilated by the ecosystems. Dust is also known to enhance N deposition by interacting with anthropogenic pollutants and neutralisation of part of the acidity of the atmosphere by crustal alkaline species. The link between the soluble iron (Fe) and phosphorus (P) atmospheric deposition and atmospheric acidity, as well as anthropogenic sources, is investigated. The global atmospheric Fe, P and N cycle are parameterized in the global 3-D chemical transport model TM4-ECPL. Both primary emissions of total and soluble Fe and P associated with dust and combustion processes are taken into account, as well as inorganic and organic N emissions. The impact of atmospheric acidity on nutrient solubility is parameterised based on experimental findings. The model results are evaluated by comparison with available observations. The impact of air-quality changes on soluble nutrient deposition is studied by performing sensitivity simulations using preindustrial, present and future emission scenarios. The response of the chemical composition of nutrient-containing aerosols to environmental changes is demonstrated and quantified. This work has been supported by ARISTEIA - PANOPLY grant co-financed by European Union (ESF) and Greek national funds NSRF.
Evaluating emissions of HCHO, HONO, NO2, and SO2 from point sources using portable Imaging DOAS
NASA Astrophysics Data System (ADS)
Pikelnaya, O.; Tsai, C.; Herndon, S. C.; Wood, E. C.; Fu, D.; Lefer, B. L.; Flynn, J. H.; Stutz, J.
2011-12-01
Our ability to quantitatively describe urban air pollution to a large extent depends on an accurate understanding of anthropogenic emissions. In areas with a high density of individual point sources of pollution, such as petrochemical facilities with multiple flares or regions with active commercial ship traffic, this is particularly challenging as access to facilities and ships is often restricted. Direct formaldehyde emissions from flares may play an important role for ozone chemistry, acting as an initial radical precursor and enhancing the degradation of co-emitted hydrocarbons. HONO is also recognized as an important OH source throughout the day. However, very little is known about direct HCHO and HONO emissions. Imaging Differential Optical Absorption Spectroscopy (I-DOAS), a relatively new remote sensing technique, provides an opportunity to investigate emissions from these sources from a distance, making this technique attractive for fence-line monitoring. In this presentation, we will describe I-DOAS measurements during the FLAIR campaign in the spring/summer of 2009. We performed measurements outside of various industrial facilities in the larger Houston area as well as in the Houston Ship Channel to visualize and quantify the emissions of HCHO, NO2, HONO, and SO2 from flares of petrochemical facilities and ship smoke stacks. We will present the column density images of pollutant plumes as well as fluxes from individual flares calculated from I-DOAS observations. Fluxes from individual flares and smoke stacks determined from the I-DOAS measurements vary widely in time and by the emission sources. We will also present HONO/NOx ratios in ship smoke stacks derived from the combination of I-DOAS and in-situ measurements, and discuss other trace gas ratios in plumes derived from the I-DOAS observations. Finally, we will show images of HCHO, NO2 and SO2 plumes from control burn forest fires observed in November of 2009 at Vandenberg Air Force Base, Santa Maria, CA.
On Road Study of Colorado Front Range Greenhouse Gases Distribution and Sources
NASA Astrophysics Data System (ADS)
Petron, G.; Hirsch, A.; Trainer, M. K.; Karion, A.; Kofler, J.; Sweeney, C.; Andrews, A.; Kolodzey, W.; Miller, B. R.; Miller, L.; Montzka, S. A.; Kitzis, D. R.; Patrick, L.; Frost, G. J.; Ryerson, T. B.; Robers, J. M.; Tans, P.
2008-12-01
The Global Monitoring Division and Chemical Sciences Division of the NOAA Earth System Research Laboratory have teamed up over the summer 2008 to experiment with a new measurement strategy to characterize greenhouse gases distribution and sources in the Colorado Front Range. Combining expertise in greenhouse gases measurements and in local to regional scales air quality study intensive campaigns, we have built the 'Hybrid Lab'. A continuous CO2 and CH4 cavity ring down spectroscopic analyzer (Picarro, Inc.), a CO gas-filter correlation instrument (Thermo Environmental, Inc.) and a continuous UV absorption ozone monitor (2B Technologies, Inc., model 202SC) have been installed securely onboard a 2006 Toyota Prius Hybrid vehicle with an inlet bringing in outside air from a few meters above the ground. To better characterize point and distributed sources, air samples were taken with a Portable Flask Package (PFP) for later multiple species analysis in the lab. A GPS unit hooked up to the ozone analyzer and another one installed on the PFP kept track of our location allowing us to map measured concentrations on the driving route using Google Earth. The Hybrid Lab went out for several drives in the vicinity of the NOAA Boulder Atmospheric Observatory (BAO) tall tower located in Erie, CO and covering areas from Boulder, Denver, Longmont, Fort Collins and Greeley. Enhancements in CO2, CO and destruction of ozone mainly reflect emissions from traffic. Methane enhancements however are clearly correlated with nearby point sources (landfill, feedlot, natural gas compressor ...) or with larger scale air masses advected from the NE Colorado, where oil and gas drilling operations are widespread. The multiple species analysis (hydrocarbons, CFCs, HFCs) of the air samples collected along the way bring insightful information about the methane sources at play. We will present results of the analysis and interpretation of the Hybrid Lab Front Range Study and conclude with perspectives on how we will adapt the measurement strategy to study CO2 anthropogenic emissions in Denver Basin.
Kirol, Christopher P; Beck, Jeffrey L; Huzurbazar, Snehalata V; Holloran, Matthew J; Miller, Scott N
2015-06-01
Conserving a declining species that is facing many threats, including overlap of its habitats with energy extraction activities, depends upon identifying and prioritizing the value of the habitats that remain. In addition, habitat quality is often compromised when source habitats are lost or fragmented due to anthropogenic development. Our objective was to build an ecological model to classify and map habitat quality in terms of source or sink dynamics for Greater Sage-Grouse (Centrocercus urophasianus) in the Atlantic Rim Project Area (ARPA), a developing coalbed natural gas field in south-central Wyoming, USA. We used occurrence and survival modeling to evaluate relationships between environmental and anthropogenic variables at multiple spatial scales and for all female summer life stages, including nesting, brood-rearing, and non-brooding females. For each life stage, we created resource selection functions (RSFs). We weighted the RSFs and combined them to form a female summer occurrence map. We modeled survival also as a function of spatial variables for nest, brood, and adult female summer survival. Our survival-models were mapped as survival probability functions individually and then combined with fixed vital rates in a fitness metric model that, when mapped, predicted habitat productivity (productivity map). Our results demonstrate a suite of environmental and anthropogenic variables at multiple scales that were predictive of occurrence and survival. We created a source-sink map by overlaying our female summer occurrence map and productivity map to predict habitats contributing to population surpluses (source habitats) or deficits (sink habitat) and low-occurrence habitats on the landscape. The source-sink map predicted that of the Sage-Grouse habitat within the ARPA, 30% was primary source, 29% was secondary source, 4% was primary sink, 6% was secondary sink, and 31% was low occurrence. Our results provide evidence that energy development and avoidance of energy infrastructure were probably reducing the amount of source habitat within the ARPA landscape. Our source-sink map provides managers with a means of prioritizing habitats for conservation planning based on source and sink dynamics. The spatial identification of high value (i.e., primary source) as well as suboptimal (i.e., primary sink) habitats allows for informed energy development to minimize effects on local wildlife populations.
Temporally delineated sources of major chemical species in high Arctic snow
NASA Astrophysics Data System (ADS)
Macdonald, Katrina M.; Sharma, Sangeeta; Toom, Desiree; Chivulescu, Alina; Platt, Andrew; Elsasser, Mike; Huang, Lin; Leaitch, Richard; Chellman, Nathan; McConnell, Joseph R.; Bozem, Heiko; Kunkel, Daniel; Duan Lei, Ying; Jeong, Cheol-Heon; Abbatt, Jonathan P. D.; Evans, Greg J.
2018-03-01
Long-range transport of aerosol from lower latitudes to the high Arctic may be a significant contributor to climate forcing in the Arctic. To identify the sources of key contaminants entering the Canadian High Arctic an intensive campaign of snow sampling was completed at Alert, Nunavut, from September 2014 to June 2015. Fresh snow samples collected every few days were analyzed for black carbon, major ions, and metals, and this rich data set provided an opportunity for a temporally refined source apportionment of snow composition via positive matrix factorization (PMF) in conjunction with FLEXPART (FLEXible PARTicle dispersion model) potential emission sensitivity analysis. Seven source factors were identified: sea salt, crustal metals, black carbon, carboxylic acids, nitrate, non-crustal metals, and sulfate. The sea salt and crustal factors showed good agreement with expected composition and primarily northern sources. High loadings of V and Se onto Factor 2, crustal metals, was consistent with expected elemental ratios, implying these metals were not primarily anthropogenic in origin. Factor 3, black carbon, was an acidic factor dominated by black carbon but with some sulfate contribution over the winter-haze season. The lack of K+ associated with this factor, a Eurasian source, and limited known forest fire events coincident with this factor's peak suggested a predominantly anthropogenic combustion source. Factor 4, carboxylic acids, was dominated by formate and acetate with a moderate correlation to available sunlight and an oceanic and North American source. A robust identification of this factor was not possible; however, atmospheric photochemical reactions, ocean microlayer reaction, and biomass burning were explored as potential contributors. Factor 5, nitrate, was an acidic factor dominated by NO3-, with a likely Eurasian source and mid-winter peak. The isolation of NO3- on a separate factor may reflect its complex atmospheric processing, though the associated source region suggests possibly anthropogenic precursors. Factor 6, non-crustal metals, showed heightened loadings of Sb, Pb, and As, and correlation with other metals traditionally associated with industrial activities. Similar to Factor 3 and 5, this factor appeared to be largely Eurasian in origin. Factor 7, sulfate, was dominated by SO42- and MS with a fall peak and high acidity. Coincident volcanic activity and northern source regions may suggest a processed SO2 source of this factor.
The anthropogenic emission and subsequent deposition of heavy metals including mercury (Hg) and lead (Pb) presents human health and environmental concerns. Although it is known that local and regional sources of these metals contribute to deposition in the Great Lakes region, it ...
In spite of the reduced flux of lead to the atmosphere from the combustion of leaded gasoline, anthropogenic sources still dominate the supply of lead to the atmosphere and the environment. Emissions from coal and oil combustion, industrial processes, and municipal incineration w...