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At least 541 records · Page 30Linked to original sources

USGS2000

Occurrence of nitrous oxide in the central High Plains aquifer, 1999

Nitrogen-enriched groundwater has been proposed as an important anthropogenic source of atmospheric nitrous oxide (N2O), yet few measurements of N2O in large aquifer systems have been made. Concentrations of N2O in water samples collected from the 124 000 km2 central High Plains aquifer in 1999 ranged from < 1 to 940 nM, with a median concentration of 29 nM (n = 123). Eighty percent of the N20 concentrations exceeded the aqueous concentration expected from equilibration with atmospheric N2O. Measurements of N2O, NO3-, and 3H in unsaturated-zone sediments, recently recharged groundwater, and older groundwater indicate that concentrations of N2O in groundwater increased over time and will likely continue to increase in the future as N-enriched water recharges the aquifer. Large concentrations of O2 and NO3- and small concentrations of NH4+ and dissolved organic carbon in the aquifer indicate that N2O in the central High Plains aquifer was produced primarily by nitrification. Calculations indicate that the flux of N2O from the central High Plains aquifer to the atmosphere from well pumping and groundwater discharge to streams was not a significant source of atmospheric N2O.Nitrogen-enriched groundwater has been proposed as an important anthropogenic source of atmospheric nitrous oxide (N2O), yet few measurements of N2O in large aquifer systems have been made. Concentrations of N2O in water samples collected from the 124000 km2 central High Plains aquifer in 1999 ranged from < 1 to 940 nM, with a median concentration of 29 nM (n = 123). Eighty percent of the N2O concentrations exceeded the aqueous concentration expected from equilibration with atmospheric N2O. Measurements of N2O, NO3-, and 3H in unsaturated-zone sediments, recently recharged groundwater, and older groundwater indicate that concentrations of N2O in groundwater increased over time and will likely continue to increase in the future as N-enriched water recharges the aquifer. Large concentrations of O2 and NO3- and small concentrations of NH4+ and dissolved organic carbon in the aquifer indicate that N2O in the central High Plains aquifer was produced primarily by nitrification. Calculations indicate that the flux of N2O from the central High Plains aquifer to the atmosphere from well pumping and groundwater discharge to streams was not a significant source of atmospheric N2O.Water samples were collected from 92 domestic wells, 16 monitoring wells and 15 public-supply wells in the High Plains Aquifer in 1999, and concentrations of nitrous oxide were measured. The groundwater concentrations ranged from less than 1 to 940 nM. Concentrations expressed as a percent of saturation in water ranged from less than 10 to 9690%. A significant decrease was noted in N2O concentrations with increasing depth of the well screen below the water table, and a significant positive correlation was found between the concentrations of N2O and nitrate. The small area-averaged N2O emission rate for the aquifer indicated that it was not an important component of the atmospheric N2O budget, but the importance could increase as groundwater N2O concentrations increase.

Environmental Science & Technology↗

USGS2006

Perchlorate in pleistocene and holocene groundwater in North-Central New Mexico

Groundwater from remote parts of the Middle Rio Grande Basin in north-central New Mexico has perchlorate (ClO 4 - ) concentrations of 0.12−1.8 μg/L. Because the water samples are mostly preanthropogenic in age (0−28 000 years) and there are no industrial sources in the study area, a natural source of the ClO 4 - is likely. Most of the samples have Br - , Cl - , and SO 4 2 - concentrations that are similar to those of modern bulk atmospheric deposition with evapotranspiration (ET) factors of about 7−40. Most of the ET values for Pleistocene recharge were nearly twice that for Holocene recharge. The NO 3 - /Cl - and ClO 4 - /Cl - ratios are more variable than those of Br - /Cl - or SO 4 2 - /Cl - . Samples thought to have recharged under the most arid conditions in the Holocene have relatively high NO 3 - /Cl - ratios and low δ 15 N values (+1 per mil (‰)) similar to those of modern bulk atmospheric N deposition. The δ 18 O values of the NO 3 - (−4 to 0 ‰) indicate that atmospheric NO 3 - was not transmitted directly to the groundwater but may have been cycled in the soils before infiltrating. Samples with nearly atmospheric NO 3 - /Cl - ratios have relatively high ClO 4 - concentrations (1.0−1.8 μg/L) with a nearly constant ClO 4 - /Cl - mole ratio of (1.4 ± 0.1) × 10 - 4 , which would be consistent with an average ClO 4 - concentration of 0.093 ± 0.005 μg/L in bulk atmospheric deposition during the late Holocene in north-central NM. Samples thought to have recharged under wetter conditions have higher δ 15 N values (+3 to +8 ‰), lower NO 3 - /Cl - ratios, and lower ClO 4 - /Cl - ratios than the ones most likely to preserve an atmospheric signal. Processes in the soils that may have depleted atmospherically derived NO 3 - also may have depleted ClO 4 - to varying degrees prior to recharge. If these interpretations are correct, then ClO 4 - concentrations of atmospheric origin as high as 4 μg/L are possible in preanthropogenic groundwater in parts of the Southwest where ET approaches a factor of 40. Higher ClO 4 - concentrations in uncontaminated groundwater could occur in recharge beneath arid areas where ET is greater than 40, where long-term accumulations of atmospheric salts are leached suddenly from dry soils, or where other (nonatmospheric) natural sources of ClO 4 - exist.

Environmental Science & Technology↗

USGS2023

Implementing a dual-spectrometer approach for improved surface reflectance estimation

Surface reflectance measurement is an integral part of the vicarious calibration of satellite sensors and the validation of satellite-derived top-of-atmosphere (TOA) and surface reflectance products. A well-known practice for estimating surface reflectance is to conduct a field campaign with a spectrometer and a calibration panel, which is labor-intensive and expensive. To address this issue, the Radiometric Calibration Network, RadCalNet, has been developed, which automatically collects surface reflectance over several selected sites. Neither of these approaches can continuously track the atmosphere, which limits their ability to compensate for atmospheric transmittance change during target measurement. This paper presents the dual-spectrometer approach that uses a stationary spectrometer dedicated to continuously tracking changes in atmospheric transmittance by staring at a calibrated reference panel while the mobile spectrometer measures the target. Simultaneous measurement of the reflectance panel and target help to transfer calibration from the stationary spectrometer to the mobile spectrometer and synchronize the measurements. In this manner, atmospheric transmittance changes during target measurement can be tracked and used to reduce the variability of the target surface reflectance. This paper uses field measurement data from combined field campaigns between different calibration groups at Brookings, South Dakota, and Landsat 8 and Landsat 9 underfly efforts over Coconino National Forest, Arizona, and Guymon, Oklahoma. Preliminary results show that even in a clear sky condition, where atmospheric transmittance changes are minimal, the precision of target surface reflectance estimated using the dual-spectrometer approach is 2–6% better than the single-spectrometer approach. The dual-spectrometer approach shows the potential for a substantial improvement in the precision of the target spectral profile when the atmospheric transmittance is changing rapidly during field measurement. Results show that during non-optimal atmospheric conditions, the dual-spectrometer approach improved the precision of the surface reflectance by 50–60% compared to the single-spectrometer approach across most spectral regions. The ability to estimate surface reflectance more precisely using the dual-spectrometer approach in different atmospheric conditions improves the vicarious calibration of optical satellite sensors and the validation of both TOA and surface reflectance products.

Remote Sensing↗

USGS2005

Gaia's breath - Global methane exhalations

Methane (CH4) is the most abundant organic compound in the Earth's atmosphere, where it acts as a greenhouse gas and thus has implications for global climate change. The current atmospheric CH4 budget, however, does not take into account geologically-sourced CH4 seepage. Geological sources of CH4 include natural macro- and micro-seeps, mud volcanoes, and other miscellaneous sources such as gas hydrates, magmatic volcanoes, geothermal regions, and mid-ocean ridges. Macro-seeps contribute ???25 Tg (teragrams) CH4/yr to the atmosphere, whereas, micro-seepage contributes perhaps 7 Tg CH4/yr. Mud volcanoes emit ???5 Tg CH4/yr, and miscellaneous sources emit ???8 Tg CH4/yr to the atmosphere. Thus, the total contribution to the atmosphere from geological sources is estimated to be 45 Tg CH4/yr, which is significant to the atmospheric organic carbon cycle and should be included in any global inventory of atmospheric CH4. We argue that the atmospheric CH4 global inventory of the Interplanetary Panel on Climate Change must be adjusted in order to incorporate geologically-sourced CH4 from naturally occurring seepage.

Marine and Petroleum Geology↗

USGS2019

Relevance of wind stress and wave-dependent ocean surface roughness on the generation of winter meteotsunamis in Northern Gulf of Mexico

Meteotsunamis associated with passing squall lines are often observed ahead of cold fronts during winter seasons in Northern Gulf of Mexico. These types of meteotsunamis occur simultaneously with wind speed variations (~5-20 m/s) and sea-level atmospheric pressure oscillations (~1-6 hPa) with periods between 2 hours to several minutes. In order to enhance understanding of meteotsunami generation and propagation mechanisms, a Coupled-Ocean-Atmosphere-Wave-Sediment Transport (COAWST) modeling system is applied to one of the most intense winter meteotsunamis measured in Northern Gulf of Mexico in the last decade (2009-2018). The model verification with sea level and atmospheric observations show that the fully-coupled model is able to reproduce the timing and intensity of the 10-m wind and sea level atmospheric pressure fluctuations. The mean bias between observed and measured wind speeds and atmospheric pressure are 1.73 m/s and 0.63 hPa respectively. The maximum meteotsunami elevation and its timing are successfully captured by modeled (with a 7% underestimation of the maximum elevation). The relative effect of atmospheric pressure and wind stress divergence on meteotsunami generation is assessed with different numerical simulations. Results indicate that both wind stress and atmospheric pressure oscillations contributed to the generation of the meteotsunami. Wind stress was the dominant force in shallow waters (<15 m in this application), while the effects of atmospheric pressure disturbances dominated over areas with Froude number close to one (~40 m in this application). During the passage of the squall line, the sea surface became rougher in a sea state characterized by young and steep local ocean waves. Compared to a purely wind-speed-dependent roughness scheme, the application of a wave-dependent roughness parameterization improved in 37% modeled meteotsunami maximum elevation.

Northern Gulf of Mexico↗

USGS2020

A synthesis of patterns of environmental mercury inputs, exposure and effects in New York State

Mercury (Hg) pollution is an environmental problem that adversely affects human and ecosystem health at local, regional, and global scales—including within New York State. More than two-thirds of the Hg currently released to the environment originates, either directly or indirectly, from human activities. Since the early 1800s, global atmospheric Hg concentrations have increased by three- to eight-fold over natural levels. In the U.S., atmospheric emissions and point-source releases to waterways increased following industrialization into the mid-1980s. Since then, water discharges have largely been curtailed. As a result, Hg emissions, atmospheric concentrations, and deposition over the past few decades have declined across the eastern U.S. Despite these decreases, Hg pollution persists. To inform policy efforts and to advance public understanding, the New York State Energy Research and Development Authority (NYSERDA) sponsored a scientific synthesis of information on Hg in New York State. This effort includes 23 papers focused on Hg in atmospheric deposition, water, fish, and wildlife published in Ecotoxicology . New York State experiences Hg contamination largely due to atmospheric deposition. Some landscapes are inherently sensitive to Hg inputs driven by the transport of inorganic Hg to zones of methylation, the conversion of inorganic Hg to methylmercury, and the bioaccumulation and biomagnification along food webs. Mercury concentrations exceed human and ecological risk thresholds in many areas of New York State, particularly the Adirondacks, Catskills, and parts of Long Island. Mercury concentrations in some biota have declined in the Eastern Great Lakes Lowlands and the Northeastern Highlands over the last four decades, concurrent with decreases in water releases and air emissions from regional and U.S. sources. However, widespread changes have not occurred in other ecoregions of New York State. While the timing and magnitude of the response of Hg levels in biota varies, policies expected to further diminish Hg emissions should continue to decrease Hg concentrations in food webs, yielding benefits to the fish, wildlife, and people of New York State. Anticipated improvements in the Hg status of aquatic ecosystems are likely to be greatest for inland surface waters and should be roughly proportional to declines in atmospheric Hg deposition. Efforts that advance recovery from Hg pollution in recent years have yielded significant progress, but Hg remains a pollutant of concern. Indeed, due to this extensive compilation of Hg observations in biota, it appears that the extent and intensity of the contamination on the New York landscape and waterscape is greater than previously recognized. Understanding the extent of Hg contamination and recovery following decreases in atmospheric Hg deposition will require further study, underscoring the need to continue existing monitoring efforts.

New York↗

USGS2016

Carbon and oxygen isotopic composition of coal and carbon dioxide derived from laboratory coal combustion: A preliminary study

The concentration of carbon dioxide (CO 2 ) in the atmosphere has dramatically increased from the start of the industrial revolution in the mid-1700s to present levels exceeding 400 ppm. Carbon dioxide derived from fossil fuel combustion is a greenhouse gas and a major contributor to on-going climate change. Carbon and oxygen stable isotope geochemistry is a useful tool to help model and predict the contributions of anthropogenic sources of CO 2 in the global carbon cycle. Surprisingly few studies have addressed the carbon and oxygen isotopic composition of CO 2 derived from coal combustion. The goal of this study is to document the relationships between the carbon and oxygen isotope signatures of coal and signatures of the CO 2 produced from laboratory coal combustion in atmospheric conditions. Six coal samples were selected that represent various geologic ages (Carboniferous to Tertiary) and coal ranks (lignite to bituminous). Duplicate splits of the six coal samples were ignited and partially combusted in the laboratory at atmospheric conditions. The resulting coal-combustion gases were collected and the molecular composition of the collected gases and isotopic analyses of δ 13 C of CO 2 , δ 13 C of CH 4 , and δ 18 O of CO 2 were analysed by a commercial laboratory. Splits (~ 1 g) of the un-combusted dried ground coal samples were analyzed for δ 13 C and δ 18 O by the U.S. Geological Survey Reston Stable Isotope Laboratory. The major findings of this preliminary work indicate that the isotopic signatures of δ 13 C (relative to the Vienna Pee Dee Belemnite scale, VPDB) of CO 2 resulting from coal combustion are similar to the δ 13 C VPDB signature of the bulk coal (− 28.46 to − 23.86 ‰) and are not similar to atmospheric δ 13 C VPDB of CO 2 (~ − 8 ‰, see http://www.esrl.noaa.gov/gmd/outreach/isotopes/c13tellsus.html ). The δ 18 O values of bulk coal are strongly correlated to the coal dry ash yields and appear to have little or no influence on the δ 18 O values of CO 2 resulting from coal combustion in open atmospheric conditions. There is a wide range of δ 13 C values of coal reported in the literature and the δ 13 C values from this study generally follow reported ranges for higher plants over geologic time. The values of δ 18 O (relative to Vienna Standard Mean Ocean Water) of CO 2 derived from atmospheric combustion of coal and other high-carbon fuels (peat and coal) range from + 19.03 to + 27.03‰ and are similar to atmospheric oxygen δ 18 O VSMOW values which average + 23.8‰. Further work is needed on a broader set of samples to better define the relationships between coal composition and combustion-derived gases.

International Journal of Coal Geology↗

USGS2007

Carbon isotopic compositions of organic matter across continental Cretaceous-Tertiary (K-T) boundary sections: Implications for paleoenvironment after the K-T impact event

To assess the environmental perturbation induced by the impact event that marks the Cretaceous-Tertiary (K-T) boundary, concentrations and isotopic compositions of bulk organic carbon were determined in sedimentary rocks that span the terrestrial K-T boundary at Dogie Creek, Montana, and Brownie Butte, Wyoming in the Western Interior of the United States. The boundary clays at both sites are not bounded by coals. Although coals consist mainly of organic matter derived from plant tissue, siliceous sedimentary rocks, such as shale and clay, may contain organic matter derived from microbiota as well as plants. Coals record ??13C values of plant-derived organic matter, reflecting the ??13C value of atmospheric CO2, whereas siliceous sedimentary rocks record the ??13C values of organic matter derived from plants and microbiota. The microbiota ??13C value reflects not only the ??13C value of atmospheric CO2, but also biological productivity. Therefore, the siliceous rocks from these sites yields information that differs from that obtained previously from coal beds. Across the freshwater K-T boundary at Brownie Butte, the ??13C values decrease by 2.6??? (from - 26.15??? below the boundary clay to - 28.78??? above the boundary clay), similar to the trend in carbonate at marine K-T sites. This means that the organic ??13C values reflect the variation of ??13C of atmospheric CO2, which is in equilibrium with carbon isotopes at the ocean surface. Although a decrease in ??13C values is observed across the K-T boundary at Dogie Creek (from - 25.32??? below the boundary clay to - 26.11??? above the boundary clay), the degree of ??13C-decrease at Dogie Creek is smaller than that at Brownie Butte and that for marine carbonate. About 2??? decrease in ??13C of atmospheric CO2 was expected from the ??13C variation of marine carbonate at the K-T boundary. This ??13C-decrease of atmospheric CO2 should affect the ??13C values of organic matter derived from plant tissue. As such a decrease in ??13C value was not observed at Dogie Creek, a process that compensates the ??13C-decrease of atmospheric CO2 should be involved. For example, the enhanced contribution of 13C-enriched organic matter derived from algae in a high-productivity environment could be responsible. The ??13C values of algal organic matter become higher than, and thus distinguishable from, those of plant organic matter in situations with high productivity, where dissolved HCO3- becomes an important carbon source, as well as dissolved CO2. As the ??13C-decrease of atmospheric CO2 reflected a reduction of marine productivity, the compensation of the ??13C decrease by the enhanced activity of the terrestrial microbiota means that the microbiota at freshwater environment recovered more rapidly than those in the marine environment. A distinct positive ??13C excursion of 2??? in the K-T boundary clays is superimposed on the overall decreasing trend at Dogie Creek; this coincides with an increase in the content of organic carbon. We conclude that the K-T boundary clays include 13C-enriched organic matter derived from highly productive algae. Such a high biological productivity was induced by phenomena resulting from the K-T impact, such as nitrogen fertilization and/or eutrophication induced by enhanced sulfide formation. The high productivity recorded in the K-T boundary clays means that the freshwater environments (in contrast to marine environments) recovered rapidly enough to almost immediately (within 10??yr) respond to the impact-related environmental perturbations. ?? 2006 Elsevier B.V. All rights reserved.

Earth and Planetary Science Letters↗

USGS2009

Contrasting residence times and fluxes of water and sulfate in two small forested watersheds in Virginia, USA

Watershed mass balances for solutes of atmospheric origin may be complicated by the residence times of water and solutes at various time scales. In two small forested headwater catchments in the Appalachian Mountains of Virginia, USA, mean annual export rates of SO 4 = differ by a factor of 2, and seasonal variations in SO 4 = concentrations in atmospheric deposition and stream water are out of phase. These features were investigated by comparing 3 H, 35 S, δ 34 S, δ 2 H, δ 18 O, δ 3 He, CFC-12, SF 6 , and chemical analyses of open deposition, throughfall, stream water, and spring water. The concentrations of SO 4 = and radioactive 35 S were about twice as high in throughfall as in open deposition, but the weighted composite values of 35 S/S (11.1 and 12.1 × 10 − 15 ) and δ 34 S (+ 3.8 and + 4.1‰) were similar. In both streams (Shelter Run, Mill Run), 3 H concentrations and δ 34 S values during high flow were similar to those of modern deposition, δ 2 H and δ 18 O values exhibited damped seasonal variations, and 35 S/S ratios (0–3 × 10 − 15 ) were low throughout the year, indicating inter-seasonal to inter-annual storage and release of atmospheric SO 4 = in both watersheds. In the Mill Run watershed, 3 H concentrations in stream base flow (10–13 TU) were consistent with relatively young groundwater discharge, most δ 34 S values were approximately the same as the modern atmospheric deposition values, and the annual export rate of SO 4 = was equal to or slightly greater than the modern deposition rate. In the Shelter Run watershed, 3 H concentrations in stream base flow (1–3 TU) indicate that much of the discharging ground water had been deposited prior to the onset of atmospheric nuclear bomb testing in the 1950s, base flow δ 34 S values (+ 1.6‰) were significantly lower than the modern deposition values, and the annual export rate of SO 4 = was less than the modern deposition rate. Concentrations of 3 H and 35 S in Shelter Run base flow, and of 3 H, 3 He, CFC-12, SF 6 , and 35 S in a spring discharging to Shelter Run, all were consistent with a bimodal distribution of discharging ground-water ages with approximately 5–20% less than a few years old and 75–95% more than 40 years old. These results provide evidence for 3 important time-scales of SO 4 = transport through the watersheds: (1) short-term (weekly to monthly) storage and release of dry deposition in the forest canopy between precipitation events; (2) mid-term (seasonal to interannual) cycles in net storage in the near-surface environment, and (3) long-term (decadal to centennial) storage in deep ground water that appears to be related to relatively low SO 4 = concentrations in spring discharge that dominates Shelter Run base flow. It is possible that the relatively low concentrations and low δ 34 S values of SO 4 = in spring discharge and Shelter Run base flow may reflect those of atmospheric deposition before the middle of the 20th century. In addition to storage in soils and biota, variations in ground-water residence times at a wide range of time scales may have important effects on monitoring, modeling, and predicting watershed responses to changing atmospheric deposition in small watersheds.

Science of the Total Environment↗

USGS2001

Carbon balance of the terrestrial biosphere in the twentieth century: analyses of CO 2 , climate and land use effects with four process-based ecosystem models

The concurrent effects of increasing atmospheric CO 2 concentration, climate variability, and cropland establishment and abandonment on terrestrial carbon storage between 1920 and 1992 were assessed using a standard simulation protocol with four process-based terrestrial biosphere models. Over the long-term(1920–1992), the simulations yielded a time history of terrestrial uptake that is consistent (within the uncertainty) with a long-term analysis based on ice core and atmospheric CO 2 data. Up to 1958, three of four analyses indicated a net release of carbon from terrestrial ecosystems to the atmosphere caused by cropland establishment. After 1958, all analyses indicate a net uptake of carbon by terrestrial ecosystems, primarily because of the physiological effects of rapidly rising atmospheric CO 2 . During the 1980s the simulations indicate that terrestrial ecosystems stored between 0.3 and 1.5 Pg C yr−1, which is within the uncertainty of analysis based on CO 2 and O 2 budgets. Three of the four models indicated (in accordance with O 2 evidence) that the tropics were approximately neutral while a net sink existed in ecosystems north of the tropics. Although all of the models agree that the long-term effect of climate on carbon storage has been small relative to the effects of increasing atmospheric CO 2 and land use, the models disagree as to whether climate variability and change in the twentieth century has promoted carbon storage or release. Simulated interannual variability from 1958 generally reproduced the El Niño/Southern Oscillation (ENSO)-scale variability in the atmospheric CO 2 increase, but there were substantial differences in the magnitude of interannual variability simulated by the models. The analysis of the ability of the models to simulate the changing amplitude of the seasonal cycle of atmospheric CO 2 suggested that the observed trend may be a consequence of CO 2 effects, climate variability, land use changes, or a combination of these effects. The next steps for improving the process-based simulation of historical terrestrial carbon include (1) the transfer of insight gained from stand-level process studies to improve the sensitivity of simulated carbon storage responses to changes in CO 2 and climate, (2) improvements in the data sets used to drive the models so that they incorporate the timing, extent, and types of major disturbances, (3) the enhancement of the models so that they consider major crop types and management schemes, (4) development of data sets that identify the spatial extent of major crop types and management schemes through time, and (5) the consideration of the effects of anthropogenic nitrogen deposition. The evaluation of the performance of the models in the context of a more complete consideration of the factors influencing historical terrestrial carbon dynamics is important for reducing uncertainties in representing the role of terrestrial ecosystems in future projections of the Earth system.

Global Biogeochemical Cycles↗

USGS1998

On the influence of biomass burning on the seasonal CO2 signal as observed at monitoring stations

We investigated the role of biomass burning in simulating the seasonal signal in both prognostic and diagnostic analyses. The prognostic analysis involved the High-Resolution Biosphere Model, a prognostic terrestrial biosphere model, and the coupled vegetation fire module, which together produce a prognostic data set of biomass burning. The diagnostic analysis involved the Simple Diagnostic Biosphere Model (SDBM) and the Hao and Liu [1994] diagnostic data set of biomass burning, which have been scaled to global 2 and 4 Pg C yr −1 , respectively. The monthly carbon exchange fields between the atmosphere and the biosphere with a spatial resolution of 0.5° × 0.5°, the seasonal atmosphere-ocean exchange fields, and the emissions from fossil fuels have been coupled to the three-dimensional atmospheric transport model TM2. We have chosen eight monitoring stations of the National Oceanic and Atmospheric Administration network to compare the predicted seasonal atmospheric CO 2 signals with those deduced from atmosphere-biosphere carbon exchange fluxes without any contribution from biomass burning. The prognostic analysis and the diagnostic analysis with global burning emissions of 4 Pg C yr −1 agree with respect to the change in the amplitude of the seasonal CO 2 concentration introduced through biomass burning. We find that the seasonal CO 2 signal at stations in higher northern latitudes (north of 30°N) is marginally influenced by biomass burning. For stations in tropical regions an increase in the CO 2 amplitude of more than 1 ppmv (up to 50% with respect to the observed trough to peak amplitude) has been calculated. Biomass burning at stations farther south accounts for an increase in the CO 2 amplitude of up to 59% (0.6 ppmv). A change in the phase of the seasonal CO 2 signal at tropical and southern stations has been shown to be strongly influenced by the onset of biomass burning in southern tropical Africa and America. Comparing simulated and observed seasonal CO 2 signals, we find higher discrepancies at southern tropical stations if biomass burning emissions are included. This is caused by the additional increase in the amplitude in the prognostic analysis and a phase shift in a diagnostic analysis. In contrast, at the northern tropical stations biomass burning tends to improve the estimates of the seasonal CO 2 signal in the prognostic analysis because of strengthening of the amplitude. Since the SDBM predicts the seasonal CO 2 signal reasonably well for the northern hemisphere tropical stations, no general improvement of the fit occurs if biomass burning emissions are considered.

Global Biogeochemical Cycles↗

USGS2014

An analysis of the global spatial variability of column-averaged CO 2 from SCIAMACHY and its implications for CO 2 sources and sinks

Satellite observations of carbon dioxide (CO 2 ) are important because of their potential for improving the scientific understanding of global carbon cycle processes and budgets. We present an analysis of the column-averaged dry air mole fractions of CO 2 (denoted XCO 2 ) of the Scanning Imaging Absorption Spectrometer for Atmospheric Cartography (SCIAMACHY) retrievals, which were derived from a satellite instrument with relatively long-term records (2003–2009) and with measurements sensitive to the near surface. The spatial-temporal distributions of remotely sensed XCO 2 have significant spatial heterogeneity with about 6–8% variations (367–397 ppm) during 2003–2009, challenging the traditional view that the spatial heterogeneity of atmospheric CO 2 is not significant enough (<4%) to have any large effect on terrestrial ecosystem carbon cycles. By comparison with surface measurements from the NOAA Earth System Research Laboratory (ESRL) GLOBALVIEW network, significant statistical relationships between XCO 2 and surface CO 2 were found for major ecosystems, with the exception of tropical forest. In addition, when compared with a simulated terrestrial carbon uptake from the Integrated Biosphere Simulator (IBIS) and the Emissions Database for Global Atmospheric Research (EDGAR) carbon emission inventory, the latitudinal gradient of XCO 2 seasonal amplitude was influenced by the combined effect of terrestrial carbon uptake, carbon emission, and atmospheric transport, suggesting no direct implications for terrestrial carbon sinks. From the investigation of the growth rate of XCO 2 we found that the increase of CO 2 concentration was dominated by temperature in the northern hemisphere (20–90°N) and by precipitation in the southern hemisphere (20–90°S), with the major contribution to global average occurring in the northern hemisphere. These findings indicated that the satellite measurements of atmospheric CO 2 improve not only the estimations of atmospheric inversion, but also the understanding of the terrestrial ecosystem carbon dynamics and its feedback to atmospheric CO 2 .

International Journal of Remote Sensing↗

USGS1987

Generation of liquid water on Mars through the melting of a dusty snowpack

The possibility that snowmelt could have provided liquid water for valley network formation early in the history of Mars is investigated using an optical-thermal model developed for dusty snowpacks at temperate latitudes. The heating of the postulated snow is assumed to be driven primarily by the absorption of solar radiation during clear sky conditions. Radiative heating rates are predicted as a function of depth and shown to be sensitive to the dust concentration and the size of the ice grains while the thermal conductivity is controlled by temperature, atmospheric pressure, and bulk density. Rates of metamorphism indicate that fresh fine-grained snow on Mars would evolve into moderately coarse snow during a single summer season. Results from global climate models are used to constrain the mean-annual surface temperatures for snow and the atmospheric exchange terms in the surface energy balance. Mean-annual temperatures within Martian snowpacks fail to reach the melting point for all atmospheric pressures below 1000 mbar despite a predicted temperature enhancement beneath the surface of the snowpacks. When seasonal and diurnal variations in the incident solar flux are included in the model, melting occurs at midday during the summer for a wide range of snow types and atmospheric pressures if the dust levels in the snow exceed 100 ppmw (parts per million by weight). The optimum dust concentration appears to be about 1000 ppmw. With this dust load, melting can occur in the upper few centimeters of a dense coarse-grained snow at atmospheric pressures as low as 7 mbar. Snowpack thickness and the thermal conductivity of the underlying substrate determine whether the generated snow-melt can penetrate to the snowpack base, survive basal ice formation, and subsequently become available for runoff. Under favorable conditions, liquid water becomes available for runoff at atmospheric pressures as low as 30 to 100 mbar if the substrate is composed of regolith, as is expected in the ancient cratered terrain of Mars.

Icarus↗

USGS2016

Lake oxygen isotopes as recorders of North American Rocky Mountain hydroclimate: Holocene patterns and variability at multi-decadal to millennial time scales

Lake sediment oxygen isotope records (calcium carbonate-δ 18 O) in the western North American Cordillera developed during the past decade provide substantial evidence of Pacific ocean–atmosphere forcing of hydroclimatic variability during the Holocene. Here we present an overview of 18 lake sediment δ 18 O records along with a new compilation of lake water δ 18 O and δ 2 H that are used to characterize lake sediment sensitivity to precipitation-δ 18 O in contrast to fractionation by evaporation. Of the 18 records, 14 have substantial sensitivity to evaporation. Two records reflect precipitation-δ 18 O since the middle Holocene, Jellybean and Bison Lakes, and are geographically positioned in the northern and southern regions of the study area. Their comparative analysis indicates a sequence of time-varying north–south precipitation-δ 18 O patterns that is evidence for a highly non-stationary influence by Pacific ocean–atmosphere processes on the hydroclimate of western North America. These observations are discussed within the context of previous research on North Pacific precipitation-δ 18 O based on empirical and modeling methods. The Jellybean and Bison Lake records indicate that a prominent precipitation-δ 18 O dipole (enriched-north and depleted-south) was sustained between ~ 3.5 and 1.5 ka, which contrasts with earlier Holocene patterns, and appears to indicate the onset of a dominant tropical control on North Pacific ocean–atmosphere dynamics. This remains the state of the system today. Higher frequency reversals of the north–south precipitation-δ 18 O dipole between ~ 2.5 and 1.5 ka, and during the Medieval Climate Anomaly and the Little Ice Age, also suggest more varieties of Pacific ocean–atmosphere modes than a single Pacific Decadal Oscillation (PDO) type analogue. Results indicate that further investigation of precipitation-δ 18 O patterns on short (observational) and long (Holocene) time scales is needed to improve our understanding of the processes that drive regional precipitation-δ 18 O responses to Pacific ocean–atmosphere variability, which in turn, will lead to a better understanding of internal Pacific ocean–atmosphere variability and its response to external climate forcing mechanisms.

North American Rocky Mountain↗

USGS2015

Steep spatial gradients of volcanic and marine sulfur in Hawaiian rainfall and ecosystems

Sulfur, a nutrient required by terrestrial ecosystems, is likely to be regulated by atmospheric processes in well-drained, upland settings because of its low concentration in most bedrock and generally poor retention by inorganic reactions within soils. Environmental controls on sulfur sources in unpolluted ecosystems have seldom been investigated in detail, even though the possibility of sulfur limiting primary production is much greater where atmospheric deposition of anthropogenic sulfur is low. Here we measure sulfur isotopic compositions of soils, vegetation and bulk atmospheric deposition from the Hawaiian Islands for the purpose of tracing sources of ecosystem sulfur. Hawaiian lava has a mantle-derived sulfur isotopic composition (δ 34 S VCDT) of − 0.8&permil;. Bulk deposition on the island of Maui had a δ 34 S VCDT that varied temporally, spanned a range from + 8.2 to + 19.7&permil;, and reflected isotopic mixing from three sources: sea-salt (+ 21.1&permil;), marine biogenic emissions (+ 15.6&permil;), and volcanic emissions from active vents on Kilauea Volcano (+ 0.8&permil;). A straightforward, weathering-driven transition in ecosystem sulfur sources could be interpreted in the shift from relatively low (0.0 to + 2.7&permil;) to relatively high (+ 17.8 to + 19.3&permil;) soil δ 34 S values along a 0.3 to 4100 ka soil age-gradient, and similar patterns in associated vegetation. However, sub-kilometer scale spatial variation in soil sulfur isotopic composition was found along soil transects assumed by age and mass balance to be dominated by atmospheric sulfur inputs. Soil sulfur isotopic compositions ranged from + 8.1 to + 20.3&permil; and generally decreased with increasing elevation (0–2000 m), distance from the coast (0–12 km), and annual rainfall (180–5000 mm). Such trends reflect the spatial variation in marine versus volcanic inputs from atmospheric deposition. Broadly, these results illustrate how the sources and magnitude of atmospheric deposition can exert controls over ecosystem sulfur biogeochemistry across relatively small spatial scales.

Hawaii↗

USGS2025

Ecological factors decouple Great Lakes fish mercury concentrations trends decadal declines in mercury emissions

Atmospheric mercury (Hg) deposition has been declining in North America but remains the dominant delivery mechanism to the Great Lakes. The Lakes are highly efficient at bioaccumulating methylmercury, making the fish excellent sentinels for tracking shifts in atmospheric Hg deposition. Invasive mussels have altered biogeochemical processes, prey populations and fish dietary strategies asynchronously and to varied extents across the lower four lakes, impacting fish Hg exposure. To test if fish are adapting to new biogeochemical conditions, we analyzed a 40 year fish archive for carbon and nitrogen isotope ratios and amino acid-specific nitrogen isotope ratios. To assess Hg sources, we measured Hg isotope ratios. We reconstructed and compared energetic pathways that impact fish Hg concentrations to Hg-source trends. We found fish-Hg concentrations are declining but not monotonically due to ecological disturbances. Fish-Hg isotope values, unimpacted by ecological disturbance, confirm that sources of bioaccumulated Hg shift contemporaneously with changes in atmospheric Hg concentrations. Across Lakes, the degree of responsiveness to changes in atmospheric Hg concentrations mirrors the proportion of atmospheric-delivered Hg we previously modeled. Changes in both fish concentrations and fish isotope values outpace paleolimnetic reconstructions suggesting declines in atmospheric Hg concentrations impact fish Hg more than sediment.

Great Lakes↗

USGS1998

Effect of chronic nitrogen additions on soil nitrogen fractions in red spruce stands

The responses of temperate and boreal forest ecosystems to increased nitrogen (N) inputs have been varied, and the responses of soil N pools have been difficult to measure. In this study, fractions and pool sizes of N were determined in the forest floor of red spruce stands at four sites in the northeastern U.S. to evaluate the effect of increased N inputs on forest floor N. Two of the stands received 100 kg N ha-1 yr-1 for three years, one stand received 34 kg N ha-1 yr-1 for six years, and the remaining stand received only ambient N inputs. No differences in total N content or N fractions were measured in samples of the Oie and Oa horizons between treated and control plots in the three sites that received N amendments. The predominant N fraction in these samples was amino acid N (31-45 % of total N), followed by hydrolyzable unidentified N (16-31% of total N), acid- soluble N (18-22 % of total N), and NH4/+-N (9-13 % of total N). Rates of atmospheric deposition varied greatly among the four stands. Ammonium N and amino acid N concentrations in the Oie horizon were positively related to wet N deposition, with respective r2 values of 0.92 and 0.94 (n = 4, p < 0.05). These relationships were somewhat stronger than that observed between atmospheric wet N deposition and total N content of the forest floor, suggesting that these pools retain atmospherically deposited N. The NH4/+- N pool may represent atmospherically deposited N that is incorporated into organic matter, whereas the amino acid N pool could result from microbial immobilization of atmospheric N inputs. The response of forest floor N pools to applications of N may be masked, possibly by the large soil N pool, which has been increased by the long-term input of N from atmospheric deposition, thereby overwhelming the short-term treatments.

Water, Air, & Soil Pollution↗

USGS2000

Controls on nitrogen flux in alpine/subalpine watersheds of Colorado

High‐altitude watersheds in the Front Range of Colorado show symptoms of advanced stages of nitrogen excess, despite having less nitrogen in atmospheric deposition than other regions where watersheds retain nitrogen. In two alpine/subalpine subbasins of the Loch Vale watershed, atmospheric deposition of NO 3 − plus NH 4 + was 3.2–5.5 kg N ha −1 , and watershed export was 1.8–3.9 kg N ha −1 for water years 1992–1997. Annual N export increased in years with greater input of N, but most of the additional N was retained in the watershed, indicating that parts of the ecosystem are nitrogen‐limited. Dissolved inorganic nitrogen (DIN) concentrations were greatest in subsurface water of talus landscapes, where mineralization and nitrification augment high rates of atmospheric deposition of N. Tundra landscapes had moderately high DIN concentrations, whereas forest and wetland landscapes had low concentrations, indicating little export of nitrogen from these landscapes. Between the two subbasins the catchment of Icy Brook had greater retention of nitrogen than that of Andrews Creek because of landscape and hydrologic characteristics that favor greater N assimilation in both the terrestrial and aquatic ecosystems. These results suggest that export of N from alpine/subalpine watersheds is caused by a combination of direct flushing of N from atmospheric deposition and release of N from ecosystem biogeochemical processes (N cycling). Sensitivity of alpine ecosystems in the western United States to atmospheric deposition of N is a function of landscape heterogeneity, hydrologic flow paths, and climatic extremes that limit primary productivity and microbial activity, which, in turn, control retention and release of nitrogen. Conceptual and mechanistic models of N excess that have been developed for forested ecosystems need to be modified in order to predict the response of alpine ecosystems to future changes in climate and atmospheric deposition of N.

Water Resources Research↗