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An elevational gradient in snowpack chemical loading at Glacier National Park, Montana: implications for ecosystem processes

The accumulation and melting of mountain snowpacks are major drivers of ecosystem processes in the Rocky Mountains. These include the influence of snow water equivalent (SWE) timing and amount of release on soil moisture for annual tree growth, and alpine stream discharge and temperature that control aquatic biota life histories. Snowfall also brings with it atmospheric deposition. Snowpacks will hold as much as 8 months of atmospheric deposition for release into mountain ecosystems during the spring melt. These pulses of chemicals influence soil microbiota and biogeochemical processes affecting mountain vegetation growth. Increased atmospheric nitrogen inputs recently have been documented in remote parts of Colorado's mountain systems but no baseline data exist for the Northern Rockies. We examined patterns of SWE and snow chemistry in an elevational gradient stretching from west to east over the continental divide in Glacier National Park in March 1999 and 2000. Sites ranged from 1080m to 2192m at Swiftcurrent Pass. At each site, two vertically-integrated columns of snow were sampled from snowpits up to 600cm deep and analyzed for major cations and anions. Minor differences in snow chemistry, on a volumetric basis, existed over the elvational gradient. Snowpack chemical loading estimates were calculated for NH 4 , SO 4 and NO 3 and closely followed elevational increases in SWE. NO 3 (in microequivalents/square meter) ranged from 1,000 ueq/m 2 at low elevation sites to 8,000+ ueq/m 2 for high elevation sites. Western slopes received greater amounts of SWE and chemical loads for all tested compounds.

Montana↗

Effects of acidic deposition and soil acidification on sugar maple trees in the Adirondack Mountains, New York

This study documents the effects of acidic deposition and soil acid-base chemistry on the growth, regeneration, and canopy condition of sugar maple (SM) trees in the Adirondack Mountains of New York. Sugar maple is the dominant canopy species throughout much of the northern hardwood forest in the State. A field study was conducted in 2009 in which 50 study plots within 20 small Adirondack watersheds were sampled and evaluated for soil acid-base chemistry and SM growth, canopy condition, and regeneration. Atmospheric sulfur (S) and nitrogen (N) deposition were estimated for each plot. Trees growing on soils with poor acid-base chemistry (low exchangeable calcium and % base saturation) that receive relatively high levels of atmospheric S and N deposition exhibited little to no SM seedling regeneration, decreased canopy condition, and short-to long-term growth declines compared with study plots having better soil condition and lower levels of atmospheric deposition. These results suggest that the ecosystem services provided by SM in the western and central Adirondack Mountain region, including aesthetic, cultural, and monetary values, are at risk from ongoing soil acidification caused in large part by acidic deposition.

New York↗

Acid Rain

Acid deposition, or acid rain as it is more commonly referred to, has become a widely publicized environmental issue in the U.S. over the past decade. The term usually conjures up images of fish kills, dying forests, "dead" lakes, and damage to monuments and other historic artifacts. The primary cause of acid deposition is emission of S0 2 and NO x to the atmosphere during the combustion of fossil fuels. Oxidation of these compounds in the atmosphere forms strong acids - H 2 SO 4 and HNO 3 - which are returned to the Earth in rain, snow, fog, cloud water, and as dry deposition. Although acid deposition has only recently been recognized as an environmental problem in the U.S., it is not a new phenomenon (Cogbill & Likens 1974). As early as the middle of the 17th century in England, the deleterious effects of industrial emissions on plants, animals, and humans, and the atmospheric transport of pollutants between England and France had become issues of concern (Evelyn 1661, Graunt 1662). It is interesting that well over three hundred years ago in England, recommendations were made to move industry outside of towns and build higher chimneys to spread the pollution into "distant parts." Increasing the height of smokestacks has helped alleviate local problems, but has exacerbated others. In the U.S. the height of the tallest smokestack has more than doubled, and the average height of smokestacks has tripled since the 1950s (Patrick et al 1981). This trend occurred in most industrialized nations during the 20th century and has had the effect of transforming acid rain from a local urban problem into a problem of global scale.

Book chapter↗

Tracermodel1- Excel workbook for calculation and presentation of environmental tracer data for simple groundwater mixtures: Use of chlorofluorocarbons in hydrology - a guidebook; Section III.10.3

Atmospheric environmental tracers commonly used to date groundwater on timescales of years to decades include CFC-11, CFC-12, CFC-113, SF6, 85Kr, 3 H and 3 H/3 H0 , where 3 H0 refers to initial tritium (3 H + tritiogenic 3 He) (Cook and Herczeg, 2000). Interpretation of age from environmental tracer data may be relatively simple for a water sample with a single age, but the interpretation is more complex for a sample that is a mixture of waters of varying ages. A mixture can be a natural result of convergence of flow lines to a discharge area such as a spring or stream, or it can be an artefact of sampling a long-screen well. TRACERMODEL1 contains a worksheet that can be used to determine hypothetical concentrations of atmospheric environmental tracers in water samples with several different age distributions. It is designed to permit plotting of ages and tracer concentrations in a variety of different combinations to facilitate interpretation of measurements. TRACERMODEL1 includes several different types of graphs that are linked to the calculations. The spreadsheet and accompanying graphs can be modified for specific applications. For example, the selection of atmospheric environmental tracers can be changed to reflect analytes of interest, the input tracer data can be modified to reflect local conditions or different timescales, and the analytes of interest can include other types of non-point-source contaminants, such as nitrate (Böhlke, 2002). Previous versions of this workbook have been used to evaluate field data in studies of groundwater residence time and agricultural contamination (Böhlke and Denver, 1995; Focazio et al., 1998; Katz et al., 1999; Katz et al., 2001; Plummer et al., 2001; Böhlke and Krantz, 2003; Lindsey et al., 2003).

Report↗

Regional evaluations of acid deposition effects on forests: Eastern spruce-fir

Having reviewed the results of the Integrated Forest Study (IFS) project, we now try to place the results in a larger perspective by very briefly summarizing acid deposition effects and their potential role in forest health in the several forest types represented in the IFS project. This chapter gives brief overviews of the situation in eastern spruce-fir, eastern hardwood, and southern pine forests in North America; and a very brief overview of air pollution in arid forest ecosystems in Europe (with special emphasis on the situation in Norway where the single European IFS site was located). What follows in this chapter is by no means intended to be a comprehensive review of forest health and atmospheric deposition; such an analysis would require a volume of this size for each forest type and is well beyond the scope of this chapter. A comprehensive analysis of forest health and the role of atmospheric deposition has been published for Norway spruce in Europe (Schulze et al. 1989), and one is in preparation for red spruce (Eagar and Adams, in press); the reader is referred to those volumes for a far more detailed discussion than is possible here. The intent of this chapter is merely to highlight those aspects of forest health and atmospheric deposition that have bearing on, or that can be illuminated by, the IFS results.

Book chapter↗

National Acid Precipitation Assessment Program Report to Congress: An integrated assessment

Acid deposition, more commonly known as acid rain, occurs when emissions of sulfur dioxide (SO2) and nitrogen oxides (NOx) react in the atmosphere (with water, oxygen, and oxidants) to form various acidic compounds. These acidic compounds then fall to earth in either a wet form (rain, snow, and fog) or a dry form (gases, aerosols, and particles). Prevailing winds transport the acidic compounds hundreds of miles, often across state and national borders. At certain levels the acidic compounds, including small particles such as sulfates and nitrates can cause many negative human health and environmental effects. While ecosystems are subject to many stresses, including land-use changes, climate change, and variations in hydrologic and meteorologic cycles, the scientific literature has clearly demonstrated that these pollutants can: • Degrade air quality, • Impair visibility, • Damage public health, • Acidify lakes and streams, • Harm sensitive forests, • Harm sensitive coastal ecosystems, and • Accelerate the decay of building materials, paints, and cultural artifacts such as buildings, statues, and sculptures. Title IV was passed by Congress as part of the 1990 Clean Air Act Amendments to reduce emissions of SO 2 and NO x from fossil fuel-burning power plants in order to protect ecosystems suffering damage from acid deposition and to improve air quality. At the same time, the National Acid Precipitation Assessment Program (NAPAP) was asked to periodically assess and report to Congress on the implementation of the Acid Rain Program, recent scientific knowledge surrounding acid deposition and its effects, and the reduction in acid deposition necessary to prevent adverse ecological effects. This NAPAP Report focuses primarily on emission reductions from power plants, both in terms of assessing past reductions under the Acid Rain Program and in projecting the ecological effects of additional reductions of SO 2 and NO x . It should be noted that power generation currently contributes approximately 69% of the SO 2 emissions and 22% of the NO x emissions nationwide. This contribution is decreasing as emissions from power generation continue to decrease, making the other sources of these pollutants more prominent. Modeling suggests that even if SO 2 emissions from power generation were reduced to zero, some lakes and streams would remain acidic due to acid deposition. However, there are several other regulations that reduce emissions of SO 2 and NO x from these non-power generation sources, such as the Tier II mobile source standards, the Heavy Duty Diesel standards, and the Clean Air Non-Road Diesel Rule, that have also been promulgated since 1990. These regulations, primarily designed to bring counties into attainment with fine particle and ozone air quality standards, also incidentally reduce emissions that contribute to acid deposition. Implementation of Title IV has successfully and substantially reduced emissions of SO 2 and NO x from power generation at a significantly lower cost than expected: • In 2002, SO 2 emissions were 10.2 million tons, 35% lower than 1990 emissions and 40% lower than 1980 emissions.* • In 2002, NO x emissions were 4.5 million tons, 33% lower than 1990 emissions. In addition, SO 2 emissions from all sources have decreased by 32% since 1990 and emissions of NO x from all sources have decreased by 12% since 1990. Power generating sources continue to close in on the goal of reducing power plant SO 2 emissions from 1980 levels by 50% (to 8.95 million tons) as required by the 1990 Clean Air Act. Power generating sources have also exceed­ed the goal of a two million ton reduction in NO x emissions from projected 2000 levels as required by the 1990 Clean Air Act. These emission reductions have contributed to measurable improvements in air quality, reductions in acid deposition, and the beginnings of recovery of acid-sensitive waters in some areas: • SO2 concentrations in the atmosphere (a precursor to fine particles and acid deposition) have decreased since 1990. Average annual SO2 concentrations in the Northeast in 2000–2002 were 40% lower than they were in 1989–1991, concentrations in the mid-Atlantic were 30% lower, concentrations in the Southeast were 35% lower, and concentrations in the Midwest were 45% lower. • Sulfate concentrations in the atmosphere (a major component of fine particles, especially in the East) have decreased since 1990 as well. Average annual sulfate concentrations in the Northeast and Midwest in 2000–2002 were approximately 30% lower than they were in 1989–1991, and concentrations in the mid-Atlantic and Southeast were 25% lower. • Wet sulfate deposition, a major component of acid rain, has also decreased since 1990. Average annual sulfate deposition in the Northeast in 2000–2002 was 40% lower than it was in 1989–1991, deposition in the mid-Atlantic and Midwest was 35% lower, and deposition in the Southeast was 25% lower. • Wet nitrate deposition has not decreased regionally from historical levels because of the relatively moderate NO x reduction from power plants and the continuing large contribution (over 50% of total NOx emissions) from other sources of NO x such as vehicles and nonroad vehicles. • Although visibility has begun to improve in some parts of the U.S., there is still significant impairment of visibility in many national parks and other Class I areas throughout the U.S. • Acid neutralizing capacity is beginning to rise in some surface waters in the Northeast, including lakes in the Adirondack Mountains (see graphic below). This is an indication that recovery from acidification is occurring in those areas.

Report to Congress↗

Geology and concepts of genesis of important types of uranium deposits

Uranium ore deposits occur in nearly every major rock type in the earth’s crust, and nearly all igneous, metamorphic, and sedimentary processes are capable of concentrating or dispersing uranium. However, only three types of deposits account for more than 70 percent of known Western World Reasonably Assured Resources (WWRAR): Precambrian quartz-pebble conglomerate type, Proterozoic unconformity type, and Phanerozoic sandstone type. Igneous-related processes in plutonic, volcanic, and magmatic-hydrothermal environments, considered important 25 years ago, now account for less than 10 percent of world resources known at present. The oldest known ore deposits were formed in conglomerates by placer processes under unique anoxic conditions. For the last 2.2 b.y., since oxygenation of the atmosphere, the genesis of both high- and low-temperature deposits has been dominated by three general geochemical processes: (1) oxidation of uranium to soluble U(VI) species permitting aqueous transport, perhaps most commonly as uranyl-carbonate complexes; (2) reduction, principally by C, S −2 , or Fe +2 species, to U(IV) to allow precipitation of uraninite (pitchblende), and coffinite, although the specific reductant commonly cannot be determined because these three tend to be associated geologically; and (3) igneous and metamorphic differentiation caused by exclusion of uranium from crystal structure of most rock-forming minerals. The geochemistry of uranium ore-forming processes has changed in time because of the evolution of life forms and their impact on the earth’s oxygen and carbon budgets. This evolution is reflected in changing predominance of ore types in geologic time: (1) pre-2.8 b.y. ago—no known uranium ore deposits; (2) ca. 2.8 to 2.2 b.y. ago—the first intràcratonic basins and anoxic atmosphere permitted accumulation of placer deposits of uraninite in quartz-pebble conglomerates; these deposits contain about 19 percent of the western world’s resources; (3) ca. 2.2 to 0.4 b.y. ago—following oxygenation of the atmosphere uranium was oxidized and transported as soluble U(VI) complexes to sites of reduction, commonly in organic carbon-rich marginal marine environments. Diagenesis, metamorphism, and near-surface redox enrichment subsequently formed unconformity-type, ultrametamorphic-type, and vein-type ore deposits which together contain more than 25 percent of the western world’s resources; (4) ca. 0.4 b.y. ago to present—after development of land plants the most important ore-forming process was redox-controlled deposition from ground water in continental sediments. Sandstone-type deposits, characteristic of this stage, contain about 40 percent of the western world’s resources.

Book chapter↗

Acid rain and its environmental effects: Recent scientific advances

The term ‘acid rain’ refers to atmospheric deposition of acidic constituents that impact the earth as rain, snow, particulates, gases, and vapor. Acid rain was first recognized by Ducros (1845) and subsequently described by the English chemist Robert Angus Smith (Smith, 1852) whose pioneering studies linked the sources to industrial emissions and included early observations of deleterious environmental effects (Smith, 1872). Smith's work was largely forgotten until the mid-20th century when observations began to link air pollution to the deposition of atmospheric sulfate (SO 4 2− ) and other chemical constituents, first near the metal smelter at Sudbury, Ontario, Canada, and later at locations in Europe, North America, and Australia (Gorham, 1961). Our modern understanding of acid rain as an environmental problem caused largely by regional emissions of sulfur dioxide (SO 2 ) and nitrogen oxides (NO x ) stems from observations in the 1960s and early 1970s in Sweden by Svante Odén (Odén, 1976), and in North America by Gene Likens and colleagues (Likens and Bormann, 1974). These scientists and many who followed showed the link to emissions from coal-fired power plants and other industrial sources, and documented the environmental effects of acid rain such as the acidification of surface waters and toxic effects on vegetation, fish, and other biota.

Atmospheric Environment↗

Trends in precipitation chemistry across the U.S. 1985–2017: Quantifying the benefits from 30 years of Clean Air Act amendment regulation

Acid rain was first recognized in the 1970s in North America and Europe as an atmospheric pollutant that was causing harm to ecosystems. In response, the U.S. Congress enacted Title IV of the Clean Air Act Amendments (CAA) in 1990 to reduce sulfur and nitrogen emissions from fossil fuel burning power plants. This study reports trends in wet-precipitation chemistry in response to emissions reductions implemented as part of the CAA. Trends were calculated for sulfate (SO 4 ), nitrate (NO 3 ) and ammonium (NH 4 ) from 1985 to 2017 at 168 stations operated by the National Atmospheric Deposition Program (NADP); stations were divided into 9 regions across the United States. Trend analyses were conducted for three time periods: Period 1 (1985–1999), Period 2 (2000–2017), and the entire study period (1985–2017). Seasonal and regional Kendall trend analyses reveal significant decreasing trends in mean wet-precipitation SO 4 concentrations in all 9 regions during the entire study period. The largest decreasing trends in monthly mean SO 4 precipitation-weighted concentrations were measured in the Mid-Atlantic (−1.29 μeq/l/yr), Midwest (−1.15 μeq/l/yr), and Northeast regions (−1.10 μeq/l/yr). The trends in monthly mean NO 3 concentrations were not as strong as those for SO 4 , but all of the regions had significant decreasing trends in NO 3 and again the Mid-Atlantic (−0.53 μeq/l/yr), Midwest (−0.44 μeq/l/yr), and Northeast regions (−0.50 μeq/l/yr) had the strongest trends. Trends were steepest during Period 2 for SO 4 and NO 3 , in fact for NO 3 86% of the stations had significant decreasing trends during Period 2 while only 8% of the stations had significant decreasing trends during Period 1. The stations with the highest concentrations of SO 4 and NO 3 at the beginning of the study had the strongest decreasing trends and the relations were stronger during Period 2 than Period 1. For NH 4 , 22% of the stations had statistically significant increasing trends in concentration during Period 1. The largest increasing trends in wet-precipitation NH 4 concentration occurred in the North-Central region during Period 1, Period 2 and throughout the entire study. By comparison, NH 4 trends in the Rocky-North and Rocky-South regions were about half as steep and trends in the South-Central and Midwest regions were about one-third as steep. We compared trends in SO 4 and NO 3 concentrations from NADP stations to emissions of sulfur dioxide and nitrogen oxides, respectively to determine whether there was a relation between emissions and wet-precipitation concentration trends within proximity to NADP stations. There was a statistically significant relation (r 2 = 0.62–0.69, p < 0.01) between the trend in SO 4 concentrations at individual NADP stations and total and mean sulfur dioxide (SO 2 ) emissions from power plants within a range of 750 km and 1000 km from each station. There were also significant relations between NO 3 concentration trends at NADP stations and power plant emissions of nitrogen oxides, but they were not nearly as strong (r 2 = 0.18–0.36, p < 0.01) as those for SO 4 and were strongest for emissions within a range of 1000 km and 1500 km from each NADP station. Decreases in wet-precipitation SO 4 concentrations were more consistent across regions and through time than decreases in NO 3 and SO 4 trends were more closely linked to stationary emissions sources than NO 3 trends. There were statistically significant increases in NH 4 wet-precipitation concentrations, as have been reported in previous studies, but this study found that those increases were strongest during Period 1 and were not consistent across the United States. During the first 3 years of the study period, wet-precipitation acidity was dominated by SO 4 in 8 of the 9 regions; by 2017 NO 3 dominated the acidity of wet-precipitation in 7 of the 9 regions. There has also been a downward shift in the NO 3 :NH 4 ratio of wet-precipitation as the emissions of nitrogen oxides have declined while ammonia emissions have remained essentially constant. This shift has resulted in an increase in wet-precipitation total nitrogen concentrations in 7 of the 9 regions and indicate that efforts to control NH 3 emissions will become increasingly important as emissions of nitrogen oxides continue to decline.

Atmospheric Environment↗

Physical attributes of some clouds amid a forest ecosystem's trees

Cloud or fog water collected by forest canopies of any elevation could represent significant sources of required moisture and nutrients for forest ecosystems, human consumption, and as an alternative source of water for agriculture and domestic use. The physical characteristics of fogs and other clouds have been well studied, and this information can be useful to water balance or canopy–cloud interaction model verification and to calibration or training of satellite-borne sensors to recognize atmospheric attributes, such as optical thickness, albedo, and cloud properties. These studies have taken place above-canopy or within canopy clearings and rarely amid the canopy. Simultaneous physical and chemical characteristics of clouds amid and above the trees of a mountain forest, located about 3.3 km southwest of Mt. Mitchell, NC, were collected between 13 and 22 June 1993. This paper summarizes the physical characteristics of the cloud portions amid the trees. The characteristic cloud amid the trees (including cloud and precipitation periods) contained 250 droplet/cm 3 with a mean diameter of 9.5 μm and liquid water content (LWC) of 0.11 g m −3 . The cloud droplets exhibited a bimodal distribution with modes at about 2 and 8 μm and a mean diameter near 5 μm during precipitation-free periods, whereas the concurrent above-canopy cloud droplets had a unimodal distribution with a mode near 6 μm and a mean diameter of 6 μm. The horizontal cloud water flux is nonlinearly related to the rate of collection onto that surface amid the trees, especially for the Atmospheric Sciences Research Center (ASRC) sampling device, whereas it is linear when the forward scattering spectrometer probe (FSSP) are is used. These findings suggest that statements about the effects clouds have on surfaces they encounter, which are based on above-canopy or canopy-clearing data, can be misleading, if not erroneous.

Atmospheric Research↗

Dry deposition of ammonia, nitric acid, ammonium, and nitrate to alpine tundra at Niwot Ridge, Colorado

Micrometeorological measurements and ambient air samples, analyzed for concentrations of NH3, HNO3, NH4+, and NO3-, were collected at an alpine tundra site on Niwot Ridge, Colorado. The measured concentrations were extremely low and ranged between 5 and 70ngNm-3. Dry deposition fluxes of these atmospheric species were calculated using the micrometeorological gradient method. The calculated mean flux for NH3 indicates a net deposition to the surface and indicates that NH3 contributed significantly to the total N deposition to the tundra during the August-September measurement period. Our pre-measurement estimate of the compensation point for NH3 in air above the tundra was 100-200ngNm-3; thus, a net emission of NH3 was expected given the low ambient concentrations of NH3 observed. Based on our results, however, the NH3 compensation point at this alpine tundra site appears to have been at or below about 20ngNm-3. Large deposition velocities (>2cms-1) were determined for nitrate and ammonium and may result from reactions with surface-derived aerosols. Copyright (C) 2001 Elsevier Science B.V.Micrometeorological measurements and ambient air samples, analyzed for concentrations of NH3, HNO3, NH4+, and NO3-, were collected at an alpine tundra site on Niwot Ridge, Colorado. The measured concentrations were extremely low and ranged between 5 and 70 ng N m-3. Dry deposition fluxes of these atmospheric species were calculated using the micrometeorological gradient method. The calculated mean flux for NH3 indicates a net deposition to the surface and indicates that NH3 contributed significantly to the total N deposition to the tundra during the August-September measurement period. Our pre-measurement estimate of the compensation point for NH3 in air above the tundra was 100-200 ng N m-3; thus, a net emission of NH3 was expected given the low ambient concentrations of NH3 observed. Based on our results, however, the NH3 compensation point at this alpine tundra site appears to have been at or below about 20 ng N m-3. Large deposition velocities (>2 cm s-1) were determined for nitrate and ammonium and may result from reactions with surface-derived aerosols.

Atmospheric Environment↗

Comparison of snowpack and winter wet-deposition chemistry in the Rocky Mountains, USA: Implications for winter dry deposition

Depth-integrated snowpack chemistry was measured just prior to maximum snowpack depth during the winters of 1992-1999 at 12 sites co-located with National Atmospheric Deposition Program/National Trend Network (NADP/NTN) sites in the central and southern Rocky Mountains, USA. Winter volume-weighted mean wet-deposition concentrations were calculated for the NADP/NTN sites, and the data were compared to snowpack concentrations using the paired t-test and the Wilcoxon signed-rank test. No statistically significant differences were indicated in concentrations of SO42- or NO3- (p>0.1). Small, but statistically significant differences (p???0.03) were indicated for all other solutes analyzed. Differences were largest for Ca2+ concentrations, which on average were 2.3??eql-1 (43%) higher in the snowpack than in winter NADP/NTN samples. Eolian carbonate dust appeared to influence snowpack chemistry through both wet and dry deposition, and the effect increased from north to south. Dry deposition of eolian carbonates was estimated to have neutralized an average of 6.9??eql-1 and a maximum of 12??eql-1 of snowpack acidity at the southernmost sites. The good agreement between snowpack and winter NADP/NTN SO42- and NO3- concentrations indicates that for those solutes the two data sets can be combined to increase data density in high-elevation areas, where few NADP/NTN sites exist. This combination of data sets will allow for better estimates of atmospheric deposition of SO42- and NO3- across the Rocky Mountain region.

Atmospheric Environment↗

Evaluating the effects of historical land cover change on summertime weather and climate in New Jersey: Land cover and surface energy budget changes

The 19th-century agrarian landscape of New Jersey (NJ) and the surrounding region has been extensively transformed to the present-day land cover by urbanization, reforestation, and localized areas of deforestation. This study used a mesoscale atmospheric numerical model to investigate the sensitivity of the warm season climate of NJ to these land cover changes. Reconstructed 1880s-era and present-day land cover data sets were used as surface boundary conditions for a set of simulations performed with the Regional Atmospheric Modeling System (RAMS). Three-member ensembles with historical and present-day land cover were compared to examine the sensitivity of surface air and dew point temperatures, rainfall, and the individual components of the surface energy budget to these land cover changes. Mean temperatures for the present-day landscape were 0.3-0.6??C warmer than for the historical landscape over a considerable portion of NJ and the surrounding region, with daily maximum temperatures at least 1.0??C warmer over some of the highly urbanized locations. Reforested regions, however, were slightly cooler. Dew point temperatures decreased by 0.3-0.6??C, suggesting drier, less humid near-surface air for the present-day landscape. Surface warming was generally associated with repartitioning of net radiation from latent to sensible heat flux, and conversely for cooling. While urbanization was accompanied by strong surface albedo decreases and increases in net shortwave radiation, reforestation and potential changes in forest composition have generally increased albedos and also enhanced landscape heterogeneity. The increased deciduousness of forests may have further reduced net downward longwave radiation. Copyright 2008 by the American Geophysical Union.

New Jersey↗

Improving the accuracy of S0 2 column densities and emission rates obtained from upward-looking UV-spectroscopic measurements of volcanic plumes by taking realistic radiative transfer into account

Sulfur dioxide (SO 2 ) is monitored using ultraviolet (UV) absorption spectroscopy at numerous volcanoes around the world due to its importance as a measure of volcanic activity and a tracer for other gaseous species. Recent studies have shown that failure to take realistic radiative transfer into account during the spectral retrieval of the collected data often leads to large errors in the calculated emission rates. Here, the framework for a new evaluation method which couples a radiative transfer model to the spectral retrieval is described. In it, absorption spectra are simulated, and atmospheric parameters are iteratively updated in the model until a best match to the measurement data is achieved. The evaluation algorithm is applied to two example Differential Optical Absorption Spectroscopy (DOAS) measurements conducted at Kilauea volcano (Hawaii). The resulting emission rates were 20 and 90% higher than those obtained with a conventional DOAS retrieval performed between 305 and 315 nm, respectively, depending on the different SO 2 and aerosol loads present in the volcanic plume. The internal consistency of the method was validated by measuring and modeling SO2 absorption features in a separate wavelength region around 375 nm and comparing the results. Although additional information about the measurement geometry and atmospheric conditions is needed in addition to the acquired spectral data, this method for the first time provides a means of taking realistic three-dimensional radiative transfer into account when analyzing UV-spectral absorption measurements of volcanic SO 2 plumes.

Journal of Geophysical Research D: Atmospheres↗

Synoptic analysis and WRF-Chem model simulation of dust events in the southwestern United States

Dust transported from rangelands of the Southwestern United States (US) to mountain snowpack in the Upper Colorado River Basin during spring (March-May) forces earlier and faster snowmelt, which creates problems for water resources and agriculture. To better understand the drivers of dust events, we investigated large-scale meteorology responsible for organizing two Southwest US dust events from two different dominant geographic locations: (a) the Colorado Plateau and (b) the northern Chihuahuan Desert. High-resolution Weather Research and Forecasting coupled with Chemistry model (WRF-Chem) simulations with the Air Force Weather Agency dust emission scheme incorporating a MODIS albedo-based drag-partition was used to explore land surface-atmosphere interactions driving two dust events. We identified commonalities in their meteorological setups. The meteorological analyses revealed that Polar and Sub-tropical jet stream interaction was a common upper-level meteorological feature before each of the two dust events. When the two jet streams merged, a strong northeast-directed pressure gradient upstream and over the source areas resulted in strong near-surface winds, which lifted available dust into the atmosphere. Concurrently, a strong mid-tropospheric flow developed over the dust source areas, which transported dust to the San Juan Mountains and southern Colorado snowpack. The WRF-Chem simulations reproduced both dust events, indicating that the simulations represented the dust sources that contributed to dust-on-snow events reasonably well. The representativeness of the simulated dust emission and transport in different geographic and meteorological conditions with our use of albedo-based drag partition provides a basis for additional dust-on-snow simulations to assess the hydrologic impact in the Southwest US.

southwestern United States↗

Case study modeling of turbulent and mesoscale fluxes over the BOREAS region

Results from aircraft and surface observations provided evidence for the existence of mesoscale circulations over the Boreal Ecosystem-Atmosphere Study (BOREAS) domain. Using an integrated approach that included the use of analytical modeling, numerical modeling, and data analysis, we have found that there are substantial contributions to the total budgets of heat over the BOREAS domain generated by mesoscale circulations. This effect is largest when the synoptic flow is relatively weak, yet it is present under less favorable conditions, as shown by the case study presented here. While further analysis is warranted to document this effect, the existence of mesoscale flow is not surprising, since it is related to the presence of landscape patches, including lakes, which are of a size on the order of the local Rossby radius and which have spatial differences in maximum sensible heat flux of about 300 W m-2. We have also analyzed the vertical temperature profile simulated in our case study as well as high-resolution soundings and we have found vertical profiles of temperature change above the boundary layer height, which we attribute in part to mesoscale contributions. Our conclusion is that in regions with organized landscapes, such as BOREAS, even with relatively strong synoptic winds, dynamical scaling criteria should be used to assess whether mesoscale effects should be parameterized or explicitly resolved in numerical models of the atmosphere.

Journal of Geophysical Research D: Atmospheres↗

Winter and early spring CO2 efflux from tundra communities of northern Alaska

Carbon dioxide concentrations through snow were measured in different arctic tundra communities on the North Slope of Alaska during winter and early spring of 1996. Subnivean CO 2 concentrations were always higher than atmospheric CO 2 . A steady state diffusion model was used to generate conservative estimates of CO 2 flux to the atmosphere. The magnitude of CO 2 efflux differed with tundra community type, and rates of carbon release increased from March to May. Winter CO 2 efflux was highest in riparian and snow bed communities and lowest in dry heath, upland tussock, and wet sedge communities. Snow generally accrues earlier in winter and is deeper in riparian and snow bed communities compared with other tundra communities, which are typically windswept and do not accumulate much snow during the winter. These results support the hypothesis that early and deep snow accumulation may insulate microbial populations from very cold temperatures, allowing sites with earlier snow cover to sustain higher levels of activity throughout winter compared to communities that have later developing snow cover. Extrapolating our estimates of CO 2 efflux to the entire snow-covered season indicates that total carbon flux during winter in the Arctic is 13–109 kg CO 2 -C ha −1 , depending on the vegetation community type. Wintertime CO 2 flux is a potentially important, yet largely overlooked, part of the annual carbon cycle of tundra, and carbon release during winter should be accounted for in estimates of annual carbon balance in arctic ecosystems.

Journal of Geophysical Research D: Atmospheres↗

Decadal oscillation of lakes and aquifers in the upper Great Lakes region of North America: hydroclimatic implications

We report a unique hydrologic time-series which indicates that water levels in lakes and aquifers across the upper Great Lakes region of North America have been dominated by a climatically-driven, near-decadal oscillation for at least 70 years. The historical oscillation (~13y) is remarkably consistent among small seepage lakes, groundwater tables and the two largest Laurentian Great Lakes despite substantial differences in hydrology. Hydrologic analyses indicate that the oscillation has been governed primarily by changes in the net atmospheric flux of water (P-E) and stage-dependent outflow. The oscillation is hypothetically connected to large-scale atmospheric circulation patterns originating in the mid-latitude North Pacific that support the flux of moisture into the region from the Gulf of Mexico. Recent data indicate an apparent change in the historical oscillation characterized by a ~12y downward trend beginning in 1998. Record low water levels region-wide may mark the onset of a new hydroclimatic regime.

Upper Great Lakes Region↗