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At least 163 records · Page 9Linked to original sources
USGS2009

Atmospheric correction at AERONET locations: A new science and validation data set

This paper describes an Aerosol Robotic Network (AERONET)-based Surface Reflectance Validation Network (ASRVN) and its data set of spectral surface bidirectional reflectance and albedo based on Moderate Resolution Imaging Spectroradiometer (MODIS) TERRA and AQUA data. The ASRVN is an operational data collection and processing system. It receives 50 ?? 50 km 2 ; subsets of MODIS level 1B (L1B) data from MODIS adaptive processing system and AERONET aerosol and water-vapor information. Then, it performs an atmospheric correction (AC) for about 100 AERONET sites based on accurate radiative-transfer theory with complex quality control of the input data. The ASRVN processing software consists of an L1B data gridding algorithm, a new cloud-mask (CM) algorithm based on a time-series analysis, and an AC algorithm using ancillary AERONET aerosol and water-vapor data. The AC is achieved by fitting the MODIS top-of-atmosphere measurements, accumulated for a 16-day interval, with theoretical reflectance parameterized in terms of the coefficients of the Li SparseRoss Thick (LSRT) model of the bidirectional reflectance factor (BRF). The ASRVN takes several steps to ensure high quality of results: 1) the filtering of opaque clouds by a CM algorithm; 2) the development of an aerosol filter to filter residual semitransparent and subpixel clouds, as well as cases with high inhomogeneity of aerosols in the processing area; 3) imposing the requirement of the consistency of the new solution with previously retrieved BRF and albedo; 4) rapid adjustment of the 16-day retrieval to the surface changes using the last day of measurements; and 5) development of a seasonal backup spectral BRF database to increase data coverage. The ASRVN provides a gapless or near-gapless coverage for the processing area. The gaps, caused by clouds, are filled most naturally with the latest solution for a given pixel. The ASRVN products include three parameters of the LSRT model (kL, kG, and kV), surface albedo, normalized BRF (computed for a standard viewing geometry, VZA = 0, SZA = 45??), and instantaneous BRF (or one-angle BRF value derived from the last day of MODIS measurement for specific viewing geometry) for the MODIS 500-m bands 17. The results are produced daily at a resolution of 1 km in gridded format. We also provide a cloud mask, a quality flag, and a browse bitmap image. The ASRVN data set, including 6 years of MODIS TERRA and 1.5 years of MODIS AQUA data, is available now as a standard MODIS product (MODASRVN) which can be accessed through the Level 1 and Atmosphere Archive and Distribution System website ( http://ladsweb.nascom.nasa.gov/data/search.html). It can be used for a wide range of applications including validation analysis and science research. ?? 2006 IEEE.

IEEE Transactions on Geoscience and Remote Sensing↗
USGS2012

Reconciling estimates of the contemporary North American carbon balance among terrestrial biosphere models, atmospheric inversions, and a new approach for estimating net ecosystem exchange from inventory-based data

We develop an approach for estimating net ecosystem exchange (NEE) using inventory-based information over North America (NA) for a recent 7-year period (ca. 2000–2006). The approach notably retains information on the spatial distribution of NEE, or the vertical exchange between land and atmosphere of all non-fossil fuel sources and sinks of CO 2 , while accounting for lateral transfers of forest and crop products as well as their eventual emissions. The total NEE estimate of a -327 ± 252 TgC yr -1 sink for NA was driven primarily by CO 2 uptake in the Forest Lands sector (-248 TgC yr -1 ), largely in the Northwest and Southeast regions of the US, and in the Crop Lands sector (-297 TgC yr -1 ), predominantly in the Midwest US states. These sinks are counteracted by the carbon source estimated for the Other Lands sector (+218 TgC yr -1 ), where much of the forest and crop products are assumed to be returned to the atmosphere (through livestock and human consumption). The ecosystems of Mexico are estimated to be a small net source (+18 TgC yr -1 ) due to land use change between 1993 and 2002. We compare these inventory-based estimates with results from a suite of terrestrial biosphere and atmospheric inversion models, where the mean continental-scale NEE estimate for each ensemble is -511 TgC yr -1 and -931 TgC yr -1 , respectively. In the modeling approaches, all sectors, including Other Lands, were generally estimated to be a carbon sink, driven in part by assumed CO 2 fertilization and/or lack of consideration of carbon sources from disturbances and product emissions. Additional fluxes not measured by the inventories, although highly uncertain, could add an additional -239 TgC yr -1 to the inventory-based NA sink estimate, thus suggesting some convergence with the modeling approaches.

Global Change Biology↗
USGS2008

Mercury, trace elements and organic constituents in atmospheric fine particulate matter, Shenandoah National Park, Virginia, USA: A combined approach to sampling and analysis

Compliance with U.S. air quality regulatory standards for atmospheric fine particulate matter (PM 2.5 ) is based on meeting average 24 hour (35 μ m −3 ) and yearly (15 μg m −3 ) mass‐per‐unit‐volume limits, regardless of PM 2.5 composition. Whereas this presents a workable regulatory framework, information on particle composition is needed to assess the fate and transport of PM 2.5 and determine potential environmental/human health impacts. To address these important non‐regulatory issues an integrated approach is generally used that includes (1) field sampling of atmospheric particulate matter on filter media, using a size‐limiting cyclone, or with no particle‐size limitation; and (2) chemical extraction of exposed filters and analysis of separate particulate‐bound fractions for total mercury, trace elements and organic constituents, utilising different USGS laboratories optimised for quantitative analysis of these substances. This combination of sampling and analysis allowed for a more detailed interpretation of PM 2.5 sources and potential effects, compared to measurements of PM 2.5 abundance alone. Results obtained using this combined approach are presented for a 2006 air sampling campaign in Shenandoah National Park (Virginia, USA) to assess sources of atmospheric contaminants and their potential impact on air quality in the Park. PM 2.5 was collected at two sampling sites (Big Meadows and Pinnacles) separated by 13.6 km. At both sites, element concentrations in PM 25 were low, consistent with remote or rural locations. However, element/Zr crustal abundance enrichment factors greater than 10, indicating anthropogenic input, were found for Hg, Se, S, Sb, Cd, Pb, Mo, Zn and Cu, listed in decreasing order of enrichment. Principal component analysis showed that four element associations accounted for 84% of the PM 2.5 trace element variation; these associations are interpreted to represent: (1) crustal sources (Al, REE); (2) coal combustion (Se, Sb), (3) metal production and/or mobile sources (Mo, Cd, Pb, Cu, Zn) and (4) a transient marine source (Sr, Mg). Concentrations of Hg in PM 2.5 at background levels in the single pg m −3 were shown by collection and analysis of PM 2.5 on filters and by an automated speciation analyser set up at the Big Meadows air quality site. The speciation unit revealed periodic elevation of reactive gaseous mercury (RGM) that co‐occurred with peaks in SO 2 , indicating an anthropogenic source. GC/MS total ion current chromatograms for the two sites were quite similar indicating that organic signatures were regional in extent and/or that the same compounds were present locally at each site. Calculated carbon preference index values for n ‐alkanes indicated that plant waxes rather than anthropogenic sources, were the dominant alkane source. Polycyclic aromatic hydrocarbons (PAHs) were detected, with a predominance of non‐alkylated, and higher molecular weight PAHs in this fraction, suggestive of a combustion source (fossil fuel or forest fires).

Virginia↗
USGS2014

The atmosphere can be a source of certain water soluble volatile organic compounds in urban streams

Surface water and air volatile organic compound (VOC) data from 10 U.S. Geological Survey monitoring sites were used to evaluate the potential for direct transport of VOCs from the atmosphere to urban streams. Analytical results of 87 VOC compounds were screened by evaluating the occurrence and detection levels in both water and air, and equilibrium concentrations in water (C w s ) based on the measured air concentrations. Four compounds (acetone, methyl tertiary butyl ether, toluene, and m - & p -xylene) were detected in more than 20% of water samples, in more than 10% of air samples, and more than 10% of detections in air were greater than long-term method detection levels (LTMDL) in water. Benzene was detected in more than 20% of water samples and in more than 10% of air samples. Two percent of benzene detections in air were greater than one-half the LTMDL in water. Six compounds (chloroform, p-isopropyltoluene, methylene chloride, perchloroethene, 1,1,1-trichloroethane, and trichloroethene) were detected in more than 20% of water samples and in more than 10% of air samples. Five VOCs, toluene, m - & p -xylene, methyl tert-butyl ether (MTBE), acetone, and benzene were identified as having sufficiently high concentrations in the atmosphere to be a source to urban streams. MTBE, acetone, and benzene exhibited behavior that was consistent with equilibrium concentrations in the atmosphere.

Journal of the American Water Resources Associatio↗
USGS2020

Integrating the evidence for a terrestrial carbon sink caused by increasing atmospheric CO2

Atmospheric carbon dioxide concentration ([CO 2 ]) is increasing, which increases leaf‐scale photosynthesis and intrinsic water‐use efficiency. These direct responses have the potential to increase plant growth, vegetation biomass, and soil organic matter; transferring carbon from the atmosphere into terrestrial ecosystems (a carbon sink). A substantial global terrestrial carbon sink would slow the rate of [CO 2 ] increase and thus climate change. However, ecosystem CO 2 responses are complex or confounded by concurrent changes in multiple agents of global change and evidence for a [CO 2 ]‐driven terrestrial carbon sink can appear contradictory. Here we synthesize theory and broad, multidisciplinary evidence for the effects of increasing [CO 2 ] (iCO 2 ) on the global terrestrial carbon sink. Evidence suggests a substantial increase in global photosynthesis since pre‐industrial times. Established theory, supported by experiments, indicates that iCO 2 is likely responsible for about half of the increase. Global carbon budgeting, atmospheric data, and forest inventories indicate a historical carbon sink, and these apparent iCO 2 responses are high in comparison to experiments and predictions from theory. Plant mortality and soil carbon iCO 2 responses are highly uncertain. In conclusion, a range of evidence supports a positive terrestrial carbon sink in response to iCO 2 , albeit with uncertain magnitude and strong suggestion of a role for additional agents of global change.

New Phytologist↗
USGS1979

Structure of the atmosphere of Venus up to 110 kilometers: Preliminary results from the four Pioneer Venus entry probes

The four Pioneer Venus entry probes transmitted data of good quality on the structure of the atmosphere below the clouds. Contrast of the structure below an altitude of 50 kilometers at four widely separated locations was found to be no more than a few degrees Kelvin, with slightly warmer temperatures at 30° south latitude than at 5° or 60° north. The atmosphere was stably stratified above 15 or 20 kilometers, indicating that the near-adiabatic state is maintained by the general circulation. The profiles move from near-adiabatic toward radiative equilibrium at altitudes above 40 kilometers. There appears to be a region of vertical convection above the dense cloud deck, which lies at 47.5 to 49 kilometers and at temperature levels near 360 K. The atmosphere is nearly isothermal around 100 kilometers (175 to 180 K) and appears to exhibit a sizable temperature wave between 60 and 70 kilometers. This is where the 4-day wind is believed to occur. The temperature wave may be related to some of the wavelike phenomena seen in Mariner 10 ultraviolet photographs.

Science↗
USGS1992

Increasing rates of atmospheric mercury deposition in midcontinental North America

Mercury contamination of remote lakes has been attributed to increasing deposition of atmospheric mercury, yet historic deposition rates and inputs from terrestrial sources are essentially unknown. Sediments of seven headwater lakes in Minnesota and Wisconsin were used to reconstruct regional modern and preindustrial deposition rates of mercury. Whole-basin mercury fluxes, determined from lake-wide arrays of dated cores, indicate that the annual deposition of atmospheric mercury has increased from 3.7 to 12.5 micrograms per square meter since 1850 and that 25 percent of atmospheric mercury deposition to the terrestrial catchment is exported to the lake. The deposition increase is similar among sites, implying regional or global sources for the mercury entering these lakes.

Science↗
USGS1994

Lake-atmosphere feedbacks associated with paleolakes Bonneville and Lahontan

A high-resolution, regional climate model nested within a general circulation model was used to study the interactions between the atmosphere and the large Pleistocene lakes in the Great Basin of the United States. Simulations for January and July 18,000 years ago indicate that moisture provided by synoptic-scale atmospheric circulation features was the primary component of the hydrologic budgets of Lakes Lahontan and Bonneville. In addition, lake-generated precipitation was a substantial component of the hydrologic budget of Lake Bonneville at that time. This local lake-atmosphere interaction may help explain differences in the relative sizes of these lakes 18,000 years ago.

Great Basin↗
USGS2022

Atmospheric waves and global seismoacoustic observations of the January 2022 Hunga eruption, Tonga

The 15 January 2022 climactic eruption of Hunga volcano, Tonga, produced an explosion in the atmosphere of a size that has not been documented in the modern geophysical record. The event generated a broad range of atmospheric waves observed globally by various ground-based and spaceborne instrumentation networks. Most prominent was the surface-guided Lamb wave (≲0.01 hertz), which we observed propagating for four (plus three antipodal) passages around Earth over 6 days. As measured by the Lamb wave amplitudes, the climactic Hunga explosion was comparable in size to that of the 1883 Krakatau eruption. The Hunga eruption produced remarkable globally detected infrasound (0.01 to 20 hertz), long-range (~10,000 kilometers) audible sound, and ionospheric perturbations. Seismometers worldwide recorded pure seismic and air-to-ground coupled waves. Air-to-sea coupling likely contributed to fast-arriving tsunamis. Here, we highlight exceptional observations of the atmospheric waves.

Hunga volcano↗
USGS2020

Evidence of wildfires and elevated atmospheric oxygen at the Frasnian–Famennian boundary in New York (USA): Implications for the Late Devonian mass extinction

The Devonian Period experienced significant fluctuations of atmospheric oxygen (O 2 ) levels (∼25–13%), for which the extent and timing are debated. Also characteristic of the Devonian Period, at the Frasnian–Famennian (F–F) boundary, is one of the “big five” mass extinction events of the Phanerozoic. Fossilized charcoal (inertinite) provides a record of wildfire events, which in turn can provide insight into the evolution of terrestrial ecosystems and the atmospheric composition. Here, we report organic petrology, programmed pyrolysis analysis, major and trace element analyses, and initial osmium isotope (Os i ) stratigraphy from five sections of Upper Devonian (F–F interval) from western New York, USA. These data are discussed to infer evidence of a wildfire event at the F–F boundary. Based on the evidence for a wildfire at the F–F boundary we also provide an estimate of atmospheric O 2 levels of ∼23–25% at this interval, which is in agreement with the models that predict elevated p O 2 levels during the Late Devonian. This, coupled with our Os isotope records, support the currently published Os i data that lacks any evidence for an extra-terrestrial impact or volcanic event at the F–F interval, and therefore to act as a trigger for the F–F mass extinction. The elevated O 2 level at the F–F interval inferred from this study supports the hypothesis that p CO 2 drawdown and associated climate cooling may have acted as a driving mechanism of the F–F mass extinction.

New York↗
USGS1995

Large-scale atmospheric forcing of recent trends toward early snowmelt runoff in California

Since the late 1940s, snowmelt and runoff have come increasingly early in the water year in many basins in northern and central California. This subtle trend is most pronounced in moderate-altitude basins, which are sensitive to changes in mean winter temperatures. Such basins have broad areas in which winter temperatures are near enough to freezing that small increases result initially in the formation of less snow and eventually in early snowmelt. In moderate-altitude basins of California, a declining fraction of the annual runoff has come in April–June. This decline has been compensated by increased fractions of runoff at other, mostly earlier, times in the water year. Weather stations in central California, including the central Sierra Nevada, have shown trends toward warmer winters since the 1940s. A series of regression analyses indicate that runoff timing responds equally to the observed decadal-scale trends in winter temperature and interannual temperature variations of the same magnitude, suggesting that the temperature trend is sufficient to explain the runoff-timing trends. The immediate cause of the trend toward warmer winters in California is a concurrent, long-term fluctuation in winter atmospheric circulations over the North Pacific Ocean and North America that is not immediately distinguishable from natural atmospheric variability. The fluctuation began to affect California in the 1940s, when the region of strongest low-frequency variation of winter circulations shifted to a part of the central North Pacific Ocean that is teleconnected to California temperatures. Since the late 1940s, winter wind fields have been displaced progressively southward over the central North Pacific and northward over the west coast of North America. These shifts in atmospheric circulations are associated with concurrent shifts in both West Coast air temperatures and North Pacific sea surface temperatures.

California↗
USGS2010

A multiscale and multidisciplinary investigation of ecosystem-atmosphere CO 2 exchange over the rocky mountains of colorado

A field study combined with modeling investigation demonstrated that the organization of CO2 transport by mountain terrain strongly affects the regional CO2 budget. Atmospheric dynamics can lead to complicated flows generated by inhomogeneous landscapes, topography or synoptic weather systems. The field campaign conducted of a ground deployment, the Carbon in the Mountain Experiment (CME04), and an aircraft deployment of the national Center for Atmospheric Research (NCAR) C-130, the Airborne Carbon in the Mountains Experiment (ACME04) over the period of spring to fall of 2004 to cover the seasonal variation of ecosystem-atmosphere carbon exchange. The role of the mountain circulation in CO2 transport can be played over seemingly flat terrain by mesoscale flows generated by various physical processes. The three dimensional observation strategy considered can also be applied over flat terrain.

Bulletin of the American Meteorological Society↗
USGS2017

Atmospheric rivers emerge as a global science and applications focus

Recent advances in atmospheric sciences and hydrology have identified the key role of atmo-spheric rivers (ARs) in determining the distribution of strong precipitation events in the midlatitudes. The growth of the subject is evident in the increase in scientific publications that discuss ARs (Fig. 1a). Combined with related phenomena, that is, warm conveyor belts (WCBs) and tropical moisture exports (TMEs), the frequency, position, and strength of ARs determine the occurrence of floods, droughts, and water resources in many parts of the world. A conference at the Scripps Institution of Oceanography in La Jolla, California, recently gathered over 100 experts in atmospheric, hydrologic, oceanic, and polar science; ecology; water management; and civil engineering to assess the state of AR science and to explore the need for new information. This first International Atmospheric Rivers Conference (IARC) allowed for much needed introductions and interactions across fields and regions, for example, participants came from five continents, and studies covered ARs in six continents and Greenland (Fig. 1b). IARC also fostered discussions of the status and future of AR science, and attendees strongly supported the idea of holding another IARC at the Scripps Institution of Oceanography in the summer of 2018.

Bulletin of the American Meteorological Society↗
USGS2020

Patterns and drivers of atmospheric river precipitation and hydrologic impacts across the western United States

Atmospheric rivers (ARs) significantly influence precipitation and hydrologic variability in many areas of the world, including the western United States. As ARs are increasingly recognized by the research community and the public, there is a need to more precisely quantify and communicate their hydrologic impacts, which can vary from hazardous to beneficial depending on location and on the atmospheric and land surface conditions prior to and during the AR. This study leverages 33 years of atmospheric and hydrologic data for the western United States to 1) identify how water vapor amount, wind direction and speed, temperature, and antecedent soil moisture conditions influence precipitation and hydrologic responses (runoff, recharge, and snowpack) using quantile regression and 2) identify differences in hydrologic response types and magnitudes across the study region. Results indicate that water vapor amount serves as a primary control on precipitation amounts. Holding water vapor constant, precipitation amounts vary with wind direction, depending on location, and are consistently greater at colder temperatures. Runoff efficiencies further covary with temperature and antecedent soil moisture, with precipitation falling as snow and greater available water storage in the soil column mitigating flood impacts of large AR events. This study identifies the coastal and maritime mountain ranges as areas with the greatest potential for hazardous flooding and snowfall impacts. This spatially explicit information can lead to better understanding of the conditions under which ARs of different precipitation amounts are likely to be hazardous at a given location.

Journal of Hydrometeorology↗
USGS2009

Transport of tritium contamination to the atmosphere in an arid environment

Soil–plant–atmosphere interactions strongly influence water movement in desert unsaturated zones, but little is known about how such interactions affect atmospheric release of subsurface water-borne contaminants. This 2-yr study, performed at the U.S. Geological Survey's Amargosa Desert Research Site in southern Nevada, quantified the magnitude and spatiotemporal variability of tritium (3H) transport from the shallow unsaturated zone to the atmosphere adjacent to a low-level radioactive waste (LLRW) facility. Tritium fluxes were calculated as the product of 3H concentrations in water vapor and respective evaporation and transpiration water-vapor fluxes. Quarterly measured 3H concentrations in soil water vapor and in leaf water of the dominant creosote-bush [ Larrea tridentat a (DC.) Coville] were spatially extrapolated and temporally interpolated to develop daily maps of contamination across the 0.76-km2 study area. Maximum plant and root-zone soil concentrations (4200 and 8700 Bq L−1, respectively) were measured 25 m from the LLRW facility boundary. Continuous evaporation was estimated using a Priestley–Taylor model and transpiration was computed as the difference between measured eddy-covariance evapotranspiration and estimated evaporation. The mean evaporation/transpiration ratio was 3:1. Tritium released from the study area ranged from 0.12 to 12 μg d−1 and totaled 1.5 mg (8.2 × 1010 Bq) over 2 yr. Tritium flux variability was driven spatially by proximity to 3H source areas and temporally by changes in 3H concentrations and in the partitioning between evaporation and transpiration. Evapotranspiration removed and limited penetration of precipitation beneath native vegetation and fostered upward movement and release of 3H from below the root zone.

Vadose Zone Journal↗
USGS2015

The rise of fire: Fossil charcoal in late Devonian marine shales as an indicator of expanding terrestrial ecosystems, fire, and atmospheric change

Fossil charcoal provides direct evidence for fire events that, in turn, have implications for the evolution of both terrestrial ecosystems and the atmosphere. Most of the ancient charcoal record is known from terrestrial or nearshore environments and indicates the earliest occurrences of fire in the Late Silurian. However, despite the rise in available fuel through the Devonian as vascular land plants became larger and trees and forests evolved, charcoal occurrences are very sparse until the Early Mississippian where extensive charcoal suggests well-established fire systems. We present data from the latest Devonian and Early Mississippian of North America from terrestrial and marine rocks indicating that fire became more widespread and significant at this time. This increase may be a function of rising O 2 levels and the occurrence of fire itself may have contributed to this rise through positive feedback. Recent atmospheric modeling suggests an O 2 low during the Middle Devonian (around 17.5%), with O 2 rising steadily through the Late Devonian and Early Mississippian (to 21–22%) that allowed for widespread burning for the first time. In Devonian-Mississippian marine black shales, fossil charcoal (inertinite) steadily increases up-section suggesting the rise of widespread fire systems. There is a concomitant increase in the amount of vitrinite (preserved woody and other plant tissues) that also suggests increased sources of terrestrial organic matter. Even as end Devonian glaciation was experienced, fossil charcoal continued to be a source of organic matter being introduced into the Devonian oceans. Scanning electron and reflectance microscopy of charcoal from Late Devonian terrestrial sites indicate that the fires were moderately hot (typically 500–600 °C) and burnt mainly surface vegetation dominated by herbaceous zygopterid ferns and lycopsids, rather than being produced by forest crown fires. The occurrence and relative abundance of fossil charcoal in marine black shales are significant in that these shales may provide a more continuous record of fire than is preserved in terrestrial environments. Our data support the idea that major fires are not seen in the fossil record until there is both sufficient and connected fuel and a high enough atmospheric O 2 content for it to burn.

American Journal of Science↗
USGS2000

Hydrologic, Water-Quality, Sediment Transport, and Bulk Atmospheric-Deposition Data, Guanella Pass Area, Colorado, October 1, 1994, through September 30, 1997

The hydrology and water quality of streams and lakes in the Guanella Pass area could be affected by the proposed reconstruction of the existing road over Guanella Pass between Georgetown and Grant, Colo. Data were collected during water years 1995 through 1997 (October 1, 1994, through September 30, 1997) that describe the preconstruction hydrology, water quality, sediment transport, and bulk atmospheric deposition in the Guanella Pass study area with most data being collected primarily during water years 1996-97. Data were collected at 17 stream sites, 7 road-runoff sites, 10 ground-water sites, 3 lake sites, 1 reservoir site, 2 snow-precipitation sites, and 4 bulk atmospheric-deposition sites. Data include onsite measurements of streamflow, specific conductance, pH, water temperature, turbidity, barometric pressure, and dissolved oxygen; concentrations of major ions, nutrients, and trace elements; organic carbon and trace organic compounds; suspended-sediment concentration and particle-size analyses; field measurement and depth profiles, and chlorophyll concentrations in lakes and reservoirs; trace element, nutrient, and trace organic (semi-volatiles, PCBs, and insecticides) analyses of lake and reservoir bottom sediment; and bulk atmospheric deposition rates of solids. Daily values for streamflow, maximum and minimum water temperature, specific conductance, and suspended sediment were computed at seven streamflow-monitoring stations located along South Clear Creek, Leavenworth Creek, Duck Creek, Geneva Creek, and Deer Creek.

Open-File Report↗
USGS2012

Fission products in National Atmospheric Deposition Program—Wet deposition samples prior to and following the Fukushima Dai-Ichi Nuclear Power Plant incident, March 8?April 5, 2011

Radioactive isotopes I-131, Cs-134, or Cs-137, products of uranium fission, were measured at approximately 20 percent of 167 sampled National Atmospheric Deposition Program monitoring sites in North America (primarily in the contiguous United States and Alaska) after the Fukushima Dai-Ichi Nuclear Power Plant incident on March 12, 2011. Samples from the National Atmospheric Deposition Program were analyzed for the period of March 8-April 5, 2011. Calculated 1- or 2-week radionuclide deposition fluxes at 35 sites from Alaska to Vermont ranged from 0.47 to 5,100 Becquerels per square meter during the sampling period of March 15-April 5, 2011. No fission-product isotopes were measured in National Atmospheric Deposition Program samples obtained during March 8-15, 2011, prior to the arrival of contaminated air in North America.

Puerto Rico;U.S. Virgin Islands;North America↗