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Valuing ecosystem services using benefit transfer: Separating credible and incredible approaches

Ecosystem goods and services are now widely recognized as the benefits that humans derive from the natural environment around them including abiotic (e.g. atmosphere) and biotic components. The work by Costanza et al. (1997) to value the world’s ecosystem services brought the concept of ecosystem service valuation to the attention of the world press and environmental economists working in the area of non-market valuation. The article’s US \$33 trillion estimate of these services, despite world GDP being only US \$18 trillion, was definitely headline grabbing. This ambitious effort was undertaken with reliance on transferring existing values per unit from other (often site specific) valuation studies. Benefit transfer (see Boyle and Bergstrom, 1992; Rosenberger and Loomis, 2000, 2001) involves transfers of values per unit from an area that has been valued using primary valuation methods such as contingent valuation, travel cost or hedonic property methods (Champ et al., 2003) to areas for which values are needed. Benefit transfer often provides a reasonable approximation of the benefit of unstudied ecosystem services based on transfer of benefits estimates per unit (per visitor day, per acre) from existing studies. An appropriate benefit transfer should be performed on the same spatial scale of analysis (e.g. reservoir to reservoir, city to city) as the original study. However, the reasonableness of benefit transfer may be strained when applying locally derived per acre values from studies of several thousand acres of a resource such as wetlands to hundreds of millions of acres of wetlands.

Book chapter

Microbial lime-mud production and its relation to climate change

Microbial calcification has been identified as a significant source of carbonate sediment production in modern marine and lacustrine environments around the globe. This process has been linked to the production of modern whitings and large, micritic carbonate deposits throughout the geologic record. Furthermore, carbonate deposits believed to be the result of cyanobacterial and microalgal calcification suggest that the potential exists for long-term preservation of microbial precipitates and storage of carbon dioxide (CO 2 ). Recent research has advanced our understanding of the microbial-calcification mechanism as a photosynthetically driven process. However, little is known of the effects of this process on inorganic carbon cycling or of the effects of changing climate on microbial-calcification mechanisms. Laboratory experiments on microbial cellular physiology demonstrate that cyanobacteria and green algae can utilize different carbon species for metabolism and calcification. Cyanobacterial calcification relies on bicarbonate (HCO 3 – )utilization while green algae use primarily CO 2 . Therefore, depending on which carbonate species (HCO 3 – or CO 2 ) dominates in the ocean or lacustrine environments (a condition ultimately linked to atmospheric partial pressure PCO 2 ), the origin of lime-mud production by cyanobacteria and/or algae may fluctuate through geologic time. Trends of cyanobacteria versus algal dominance in the rock record corroborate this conclusion. These results suggest that relative species abundances of calcareous cyanobacteria and algae in the Phanerozoic may serve as potential proxies for assessing paleoclimatic conditions, including fluctuations in atmospheric PCO 2 .

AAPG Studies in Geology

Stratospheric microbiology at 20 km over the Pacific Ocean

An aerobiology sampling flight at 20 km was conducted on 28 April 2008 over the Pacific Ocean (36.5° N, 118–149° W), a period of time that coincided with the movement of Asian dust across the ocean. The aim of this study was to confirm the presence of viable bacteria and fungi within a transoceanic, atmospheric bridge and to improve the resolution of flight hardware processing techniques. Isolates of the microbial strains recovered were analyzed with ribosomal ribonucleic acid (rRNA) sequencing to identify bacterial species Bacillus sp., Bacillus subtilis, Bacillus endophyticus, and the fungal genus Penicillium. Satellite imagery and ground-based radiosonde observations were used to measure dust movement and characterize the high-altitude environment at the time of collection. Considering the atmospheric residency time (7–10 days), the extreme temperature regime of the environment (-75°C), and the absence of a mechanism that could sustain particulates at high altitude, it is unlikely that our samples indicate a permanent, stratospheric ecosystem. However, the presence of viable fungi and bacteria in transoceanic stratosphere remains relevant to understanding the distribution and extent of microbial life on Earth.

Aerobiologia

Accumulation of atmospheric sulfur in some Costa Rican soils

Sulfur is one of the macronutrient elements whose sources to terrestrial ecosystems should shift from dominance by rock-weathering to atmospheric deposition as soils and underlying substrate undergo progressive weathering and leaching. However, the nature and timing of this transition is not well known. We investigated sources of sulfur to tropical rain forests growing on basalt-derived soils in the Osa Peninsula region of Costa Rica. Sulfur sources were examined using stable isotope ratios (δ 34 S) and compared to chemical indices of soil development. The most weathered soils, and the forests they supported, are dominated by atmospheric sulfur, while a less weathered soil type contains both rock-derived and atmospheric sulfur. Patterns of increasing δ 34 S with increasing soil sulfur concentration across the landscape suggest atmospheric sulfur is accumulating, and little rock-derived sulfur has been retained. Soil sulfur, minus adsorbed sulfate, is correlated with carbon and nitrogen, implying that sulfur accumulation occurs as plants and microbes incorporate sulfur into organic matter. Only the lower depth increments of the more weathered soils contained significant adsorbed sulfate. The evidence suggests a pattern of soil development in which sulfur-bearing minerals in rock, such as sulfides, weather early relative to other minerals, and the released sulfate is leached away. Sulfur added via atmospheric deposition is retained as organic matter accumulates in the soil profile. Adsorbed sulfate accumulates later, driven by changes in soil chemistry and mineralogy. These aspects of sulfur behavior during pedogenesis in this environment may hasten the transition to dominance by atmospheric sources.

Journal of Geophysical Research: Biogeosciences

Mercury speciation in piscivorous fish from mining-impacted reservoirs

Guadalupe Reservoir (GUA), California, and Lahontan Reservoir (LAH), Nevada, U.S. are both affected either directly or indirectly by the legacy of gold and silver mining in the Sierra Nevada during the nineteenth century. Analysis of total mercury in fish from these lentic systems consistently indicate elevated concentrations (>1 μg·g-1 wet weight; hereinafter, all concentrations are reported as wet weight unless indicated otherwise) well above the U.S. Environmenal Protection Agency's human consumption advisory level for fish (<0.3 μg·g-1). Replicate X-ray absorption near edge structure (XANES) analyses on largemouth bass and hybrid striped bass from GUA and LAH were performed to determine predominant chemical species of mercury accumulated by these high-trophic-level piscivores that are exposed to elevated mercury through trophic transfer in mining-impacted lentic systems. Despite distinct differences in mercury source, the proximity of the source, and concentrations of complexing ligands, results of XANES analysis clearly indicated that mercury accumulated in these individual fish from the two reservoirs were dominated by methylmercury cysteine complexes. These findings are consistent with results from commercial fish species inhabiting marine environments which are presumed to include differing mercury sources (e.g., atmospheric, hydrothermal, or benthic). The dominance of methylmercury cysteine complexes in muscle tissues of fish obtained from such contrasting environments and exposure conditions suggests that a generic toxicological model for the consumption of fish could be applicable over a wide range of ecologic settings.

Environmental Science & Technology

Simulation of nitrous oxide and nitric oxide emissions from tropical primary forests in the Costa Rican Atlantic Zone

Nitrous oxide (N 2 O) and nitric oxide (NO) are important atmospheric trace gases participating in the regulation of global climate and environment. Predictive models on the emissions of N 2 O and NO emissions from soil into the atmosphere are required. We modified the CENTURY model (Soil Sci. Soc. Am. J., 51 (1987) 1173) to simulate the emissions of N 2 O and NO from tropical primary forests in the Atlantic Zone of Costa Rica at a monthly time step. Combined fluxes of N 2 O and NO were simulated as a function of gross N mineralization and water-filled pore space (WFPS). The coefficients for partitioning N 2 O from NO were derived from field measurements (Global Biogeochem. Cycles, 8 (1994) 399). The modified CENTURY was calibrated against observations of carbon stocks in various pools of forest ecosystems of the region, and measured WFPS and emission rates of N 2 O and NO from soil to the atmosphere. WFPS is an important factor regulating nutrient cycling and emissions of N2O and NO from soils making the accuracy of the WFPS prediction central to the modeling process. To do this, we modified the hydrologic submodel and developed a new method for the prediction of WFPS at the monthly scale from daily rainfall information. The new method is based on: (1) the relationship between monthly rainfall and the number of rainfall events, and (2) the relative cumulative frequency distribution of ranked daily rainfall events. The method is generic and should be applicable to other areas. Simulated monthly average WFPS was 0.68&plusmn;0.02 &mdash; identical with the field measurement average of 0.68&plusmn;0.02 from the annual cycle observed by Keller and Reiners (Global Biogeochem. Cycles, 8 (1994) 399). Simulated fluxes of N 2 O and NO were 52.0&plusmn;9.4 mg-N m &minus;2 month &minus;1 and 6.5&plusmn;0.7 mg-N m &minus;2 month &minus;1 , respectively, compared with measured averages of 48.2&plusmn;11.0 mg-N m &minus;2 month &minus;1 and 7.1&plusmn;1.1 mg-N m &minus;2 month &minus;1 . The simulated N 2 O/NO ratio was 11.2&plusmn;1.9 compared with the measured value of 10.9&plusmn;4.7. WFPS is the dominant determinant of the fraction of gross N mineralization that is emitted from the soil as N 2 O and NO. If WFPS were not limiting during part of the year, this fraction would be 4.2%. With some periods of lower WFPS, the realized fraction is 2.2%. Because of the strong relationships between N 2 O and NO emission rates and rainfall and its derivative, WFPS, these moisture variables can be used to scale up nitrogen trace gas fluxes from sites to larger spatial scales.

Environmental Modelling and Software

Preliminary Mineralogic and Stable Isotope Studies of Altered Summit and Flank Rocks and Osceola Mudflow Deposits on Mount Rainier, Washington

About 5600 years ago part of Mount Rainier?s edifice collapsed with the resultant Osceola Mudflow traveling more than 120 km and covering an area of at least 505 km2. Mineralogic and stable isotope studies were conducted on altered rocks from outcrops near the summit and east flank of the volcano and samples of clasts and matrix from the Osceola Mudflow. Results of these analyses are used to constrain processes responsible for pre-collapse alteration and provide insight into the role of alteration in edifice instability prior to the Osceola collapse event. Jarosite, pyrite, alunite, and kaolinite occur in hydrothermally altered rock exposed in summit scarps formed by edifice collapse events and in altered rock within the east-west structural zone (EWSZ) of the volcano?s east flank. Deposits of the Osceola Mudflow contain clasts of variably altered and unaltered andesite within a clay-rich matrix. Minerals detected in samples from the edifice are also present in many of the clasts. The matrix includes abundant smectite, kaolinite and variably abundant jarosite. Hydrothermal fluid compositions calculated from hydrogen and oxygen isotope data of alunite, and smectite on Mount Rainier reflect mixing of magmatic and meteoric waters. The range in the dD values of modern meteoric water on the volcano (-85 to 155?) reflect the influence of elevation on the dD of precipitation. The d34S and d18OSO4 values of alunite, gypsum and jarosite are distinct but together range from 1.7 to 17.6? and -12.3 to 15.0?, respectively; both parameters increase from jarosite to gypsum to alunite. The variations in sulfur isotope composition are attributed to the varying contributions of disproportionation of magmatic SO2, the supergene oxidation of hydrothermal pyrite and possible oxidation of H2S to the parent aqueous sulfate. The 18OSO4 values of jarosite are the lowest recorded for the mineral, consistent with a supergene origin. The mineralogy and isotope composition of alteration minerals define two and possibly three environments of alteration. At deeper levels magmatic vapor, H2S, SO2 and other gases from venting magmas migrated upward and condensed into the meteoric water. Disproportionation of SO2 into aqueous sulfate and H2S resulted in acid-sulfate (alunite + kaolinite + pyrite) and related argillic and propylitic alteration envelopes in a magmatic hydrothermal environment. At shallow levels H2S reacted with andesite to form pyrite that is associated with smectite along fractures on both the flanks and upper edifice. It is not clear to what extent H2S was oxidized by atmospheric O2 to form aqueous sulfate in a steam-heated environment. Near the ground surface, pyrite is oxidized by atmospheric oxygen resulting in soluble iron-and aluminum-hydroxysulfates. These supergene hydroxysulfates, which may also form around fumaroles from the oxidation of H2S, are subject to continuous solution and redeposition.

Open-File Report

Atmospheric mercury and fine particulate matter in coastal New England: implications for mercury and trace element sources in the northeastern United States

Intensive sampling of ambient atmospheric fine particulate matter was conducted at Woods Hole, Massachusetts over a four-month period from 3 April to 29 July, 2008, in conjunction with year-long deployment of the USGS Mobile Mercury Lab. Results were obtained for trace elements in fine particulate matter concurrently with determination of ambient atmospheric mercury speciation and concentrations of ancillary gasses (SO 2 , NO x , and O 3 ). For particulate matter, trace element enrichment factors greater than 10 relative to crustal background values were found for As, Bi, Cd, Cu, Hg, Pb, Sb, V, and Zn, indicating contribution of these elements by anthropogenic sources. For other elements, enrichments are consistent with natural marine (Na, Ca, Mg, Sr) or crustal (Ba, Ce, Co, Cs, Fe, Ga, La, Rb, Sc, Th, Ti, U, Y) sources, respectively. Positive matrix factorization was used together with concentration weighted air-mass back trajectories to better define element sources and their locations. Our analysis, based on events exhibiting the 10% highest PM 2.5 contributions for each source category, identifies coal-fired power stations concentrated in the U.S. Ohio Valley, metal smelting in eastern Canada, and marine and crustal sources showing surprisingly similar back trajectories, at times each sampling Atlantic coastal airsheds. This pattern is consistent with contribution of Saharan dust by a summer maximum at the latitude of Florida and northward transport up the Atlantic Coast by clockwise circulation of the summer Bermuda High. Results for mercury speciation show diurnal production of RGM by photochemical oxidation of Hg° in a marine environment, and periodic traverse of the study area by correlated RGM-SO 2 (NO x ) plumes, indicative of coal combustion sources.

Massachusetts

U.S. Geological Survey Methodology Development for Ecological Carbon Assessment and Monitoring

Ecological carbon sequestration refers to transfer and storage of atmospheric carbon in vegetation, soils, and aquatic environments to help offset the net increase from carbon emissions. Understanding capacities, associated opportunities, and risks of vegetated ecosystems to sequester carbon provides science information to support formulation of policies governing climate change mitigation, adaptation, and land-management strategies. Section 712 of the Energy Independence and Security Act (EISA) of 2007 mandates the Department of the Interior to develop a methodology and assess the capacity of our nation's ecosystems for ecological carbon sequestration and greenhouse gas (GHG) flux mitigation. The U.S. Geological Survey (USGS) LandCarbon Project is responding to the Department of Interior's request to develop a methodology that meets specific EISA requirements.

Fact Sheet

Evaluation of candidate rain gages for upgrading precipitation measurement tools for the National Atmospheric Deposition Program

The National Atmospheric Deposition Program (NADP) was established in 1977 to investigate atmospheric deposition and its effects on the environment. Since its establishment, precipitation records have been obtained at all NADP sites using a gage developed approximately 50 years ago-the Belfort 5-780 mechanical rain gage. In 1998 and 1999, a study was done by the U.S. Geological Survey to evaluate four recently developed, technologically advanced rain gages as possible replacement candidates for the mechanical gage currently (2002) in use by the NADP. The gage types evaluated were the Belfort 3200, Geonor T-200, ETI Noah II, and the OTT PLUVIO. The Belfort 5-780 was included in the study to compare the performance of the rain gage currently (2002) used by NADP to the performance of the more recently developed gages. As a reference gage, the NovaLynx Model 260-2510 National Weather Service type stick gage also was included in the study. Two individual gages of each type were included in the study to evaluate precision between gages of the same type. A two-phase evaluation was completed. Phase I consisted of indoor bench tests with known amounts of simulated rainfall applied in 20 individual tests. Phase II consisted of outdoor testing by collecting precipitation during a 26-week period near Bay St. Louis, Mississippi. The ETI Noah II, OTT PLUVIO, and NovaLynx stick gages consistently recorded depths more commensurate with the amounts of applied simulated rainfall in Phase I testing than the Geonor T-200, Belfort 5-780, and Belfort 3200 gages. Gages where both the median difference between the measured and applied simulated rainfall and the interquartile range of all of their measured minus applied simulated rainfall differences were small (less than or equal to 0.01 inch) were judged to have performed very well in Phase I testing. The median and interquartile-range values were 0.01 inch or less for each of the ETI Noah II gages, OTT PLUVIO gages, and NovaLynx stick gages. The performance of the Geonor T-200 and Belfort 3200 gages was affected by technical problems during Phase I testing. As part of the evaluation of Phase II results, the average weekly precipitation totals obtained from the Belfort 5-780 gages and from each of the gages under consideration as possible replacements for the Belfort 5-780 gage were all compared with the average precipitation weekly totals obtained from two NovaLynx stick gages. The median absolute differences between a particular gage model and the NovaLynx stick reference gage for the 26 weeks of outdoor testing ranged from 0.04 inch for the ETI Noah II and OTT PLUVIO gages to 0.06 inch for the Geonor T-200. The total absolute difference between a particular gage type and the reference gage ranged from 1.23 inches for the Belfort 5-780 to 1.83 inches for the Geonor T-200 gages. Because the Belfort 3200 gages were inoperable for most of the Phase II testing, it is not meaningful to include the results from that gage type in a calculation of median or total absolute differences. The OTT PLUVIO proved to be the most reliable gage in Phase I and II testing, operating trouble free over the duration of the study.

Water-Resources Investigations Report

Evaluation of OTT PLUVIO Precipitation Gage versus Belfort Universal Precipitation Gage 5-780 for the National Atmospheric Deposition Program

The National Atmospheric Deposition Program, a cooperative effort supported by Federal, State, and local agencies, and Indian Tribes, was established in 1977 to study atmospheric deposition and its impact on the environment. The program's National Trends Network now includes wet-deposition networks at more than 250 sites across the United States, Canada, Puerto Rico, and the Virgin Islands. Precipitation amounts are currently measured using a Belfort Universal Precipitation Gage 5-780, which involves technology that is more than 50 years old. In 1999, a three-phase study was begun to evaluate several weighing, all-weather precipitation gages to find a possible replacement for the Belfort Universal Precipitation Gage 5-780. One gage that performed consistently well in phase I and II testing was the OTT PLUVIO Precipitation Gage. Phase III of the study, discussed herein, was to determine the accuracy and comparability of the data sets collected by the OTT PLUVIO Precipitation Gages and the existing Belfort Universal Precipitation Gage 5-780. Seven OTT PLUVIO Precipitation Gages were installed at six National Trends Network sites across the country for a data-collection period of approximately 18 months. The NovaLynx Model 260-2510 Standard Rain and Snow Gage also was used, as a reference, at two of the sites. Paired t-tests analysis showed no significant differences in precipitation measurements between the Belfort Universal Precipitation Gage 5-780 and the OTT PLUVIO Precipitation Gages at three of the six sites. When the false positives were removed from the precipitation-event data sets, the gages at all sites were in agreement and the paired t-tests showed the gage measurements were not significantly different. A false positive is defined as a zero response from the Belfort Universal Precipitation Gage 5-780 concurrent with a recorded response from the OTT PLUVIO Precipitation Gage.

Water-Resources Investigations Report

Variations in the global carbon cycle during the Cretaceous related to climate, volcanism, and changes in atmospheric CO2

The stratigraphic record from both deep-sea and shallow-water depositional environments indicates that during late Aptian through Cenomanian time (1) global climates were considerably warmer than at present; (2) latitudinal gradients of atmospheric and oceanic temperatures were considerably less than at present; (3) rates of accumulation of organic matter of both marine and terrestrial origin were as high as or higher than during any other interval in the Mesozoic or Cenozoic; (4) the rate and volume of accumulation of CaCO 3 in the deep sea were reduced in response to a marked shoaling of the carbonate compensation depth; (5) seafloor spreading rates were somewhat more rapid than at any other time in the Cretaceous or Cenozoic; (6) off-ridge volcanism was intense and widespread, particularly in the ancestral Pacific Ocean basin; and (7) sea level was relatively high, forming widespread areas of shallow shelf seas. A marked increase in the rate of CO 2 outgassing due to volcanic activity between about 110 and 70 m.y. ago may have resulted in a buildup of atmospheric CO 2. A significant fraction of this atmospheric CO 2 may have been reduced by an increase in the production and burial of terrestrial organic carbon. Some excess CO 2may have been consumed by marine algal photosynthesis, but marine productivity apparently was low during the Aptian-Albian relative to terrestrial productivity. Terrestrial productivity also may have been stimulated by increased rainfall that resulted 504 from a warm global climate and increased marine transgression as well as by the higher CO 2.

Book chapter

In situ recording of Mars soundscape

Prior to the Perseverance rover landing, the acoustic environment of Mars was unknown. Models predicted that: (i) atmospheric turbulence changes at centimeter scales or smaller at the point where molecular viscosity converts kinetic energy into heat 1 , (ii) the speed of sound varies at the surface with frequency 2,3 , and (iii) high frequency waves are strongly attenuated with distance in CO 2 2–4 . However, theoretical models were uncertain because of a lack of experimental data at low pressure, and the difficulty to characterize turbulence or attenuation in a closed environment. Here using Perseverance microphone recordings, we present the first characterization of Mars’ acoustic environment and pressure fluctuations in the audible range and beyond, from 20 Hz to 50 kHz. We find that atmospheric sounds extend measurements of pressure variations down to 1,000 times smaller scales than ever observed before, revealing a dissipative regime extending over 5 orders of magnitude in energy. Using point sources of sound (Ingenuity rotorcraft, laser-induced sparks), we highlight two distinct values for the speed of sound that are ~10 m/s apart below and above 240 Hz, a unique characteristic of low-pressure CO 2 -dominated atmosphere. We also provide the acoustic attenuation with distance above 2 kHz, allowing us to elucidate the large contribution of the CO 2 vibrational relaxation in the audible range. These results establish a ground truth for modelling of acoustic processes, which is critical for studies in atmospheres like Mars and Venus ones.

Nature

40Ar/36Ar analyses of historic lava flows

The ratio 40 Ar/ 36 Ar was measured for 26 subaerial historic lava flows. Approximately one-third of the samples had 40 Ar/ 36 Ar ratios either higher or lower than the atmospheric value of 295.5 at the 95% confidence level. Excess radiogenic 40 Ar in five flows ranged from about 1 × 10 −13 to 1.5 × 10 −12 mol/g. Possible excess 36 Ar in three flows was on the order of 10 −16 to 10 −15 mol/g. Upper 95% confidence limits for excess 40 Ar in samples with normal 40 Ar/ 36 Ar ratios are generally less than 3 × 10 −13 mol/g. The origin of the excess 36 Ar is unknown but it may be due either to the incorporation of primitive argon that has been stored in the mantle in very low potassium environments or to enrichment in 36 Ar as atmospheric argon diffuses into the rocks after they cool.

Earth and Planetary Science Letters

Global environmental databases from CEOS agencies

The Committee on Earth Observation Satellites (CEOS) is an international organization charged with coordinating international civil spaceborne missions designed to observe and study planet Earth. Comprising 44 space agencies and other national and international organizations, CEOS is recognized as the major international forum for the coordination of Earth observation satellite programs and for the interaction of these programs with users of satellite data worldwide. CEOS was created in 1984 in response to a recommendation from the Economic Summit of Industrialized Nations Working Group on Growth, Technology, and Employment’s Panel of Experts on Satellite Remote Sensing. This group recognized the multidisciplinary nature of satellite Earth observation and the value of coordination across all proposed missions. The CEOS members collect, maintain, apply, and make available data from space missions that encompass the atmospheric, terrestrial, and oceanographic fields. Collectively, these members possess petabytes of Earth observation data critical to understanding the Earth environment. Uses include monitoring oil slicks, evaluating human-induced changes to the atmosphere, determining mineral exploration areas, assessing the environmental effects of volcanic eruptions, measuring the growth of urban areas, determining where landscapes have changed because of urban growth trends, improving the efficiency of fishing as a world food stock, monitoring pest infestation, managing crop production, predicting climate and weather, and numerous other applications vital to industry, national infrastructures, and the world as a whole. The vast amount of satellite obtained, environmental data the CEOS members possess represents a fertile resource for researchers worldwide to exploit.

Conference Paper

Methane clumped isotopologue variability from ebullition in a mid-latitude lake

Methane is a greenhouse gas and is an important component of carbon cycling in freshwater environments. Isotope ratios of methane ( 13 C/ 12 C and D/H) are used extensively as tracers to identify methane sources. Recent advances in the measurement of clumped methane isotopologues ( 13 CH 3 D, 12 CH 2 D 2 ) offer new opportunities to constrain sources and sinks of atmospheric methane. Previous measurements of clumped methane isotopologues from freshwater environments have been spatially and temporally limited. The abundance of 13 CH 3 D and methane flux from ebullition in the deep basin of Upper Mystic Lake were measured from May to November 2021 to characterize the source isotopologue signatures and methane fluxes for mid-latitude lakes. The trends in δ 13 C and δD values support decreased methane oxidation in the early summer compared to fall. The Δ 13 CH 3 D values from this study range from 2.0 to 4.2‰, reflecting methane oxidation occurring anaerobically in lake sediments and euxinic bottom waters at sample sites. The relatively large variation in the Δ 13 CH 3 D values observed within this lake basin aligns with previous observations of bubbles from arctic lakes. The values of Δ 13 CH 3 D do not correlate with methane flux, suggesting that Δ 13 CH 3 D measurements from background ebullition are not sensitive as a proxy for ebullition rates. This study presents a uniquely large ( n = 40) set of freshwater Δ 13 CH 3 D values from a single lake basin, which we use to recommend a sampling strategy of ≥9 samples to constrain the Δ 13 CH 3 D source signal within ∼0.5‰ from similar environments. This data demonstrates the utility of clumped methane isotopologues to gain insights into local biogeochemical processes from field studies and points to the challenge of using clumped isotopologue measurements to constrain global freshwater–methane sources to the atmosphere.

ACS Earth and Space Chemistry

Measurement-derived heat-budget approaches for simulating coastal wetland temperature with a hydrodynamic model

Numerical modeling is needed to predict environmental temperatures, which affect a number of biota in southern Florida, U.S.A., such as the West Indian manatee (Trichechus manatus), which uses thermal basins for refuge from lethal winter cold fronts. To numerically simulate heat-transport through a dynamic coastal wetland region, an algorithm was developed for the FTLOADDS coupled hydrodynamic surface-water/ground-water model that uses formulations and coefficients suited to the coastal wetland thermal environment. In this study, two field sites provided atmospheric data to develop coefficients for the heat flux terms representing this particular study area. Several methods were examined to represent the heat-flux components used to compute temperature. A Dalton equation was compared with a Penman formulation for latent heat computations, producing similar daily-average temperatures. Simulation of heat-transport in the southern Everglades indicates that the model represents the daily fluctuation in coastal temperatures better than at inland locations; possibly due to the lack of information on the spatial variations in heat-transport parameters such as soil heat capacity and surface albedo. These simulation results indicate that the new formulation is suitable for defining the existing thermohydrologic system and evaluating the ecological effect of proposed restoration efforts in the southern Everglades of Florida.

Florida

Mercury loading and methylmercury production and cycling in high-altitude lakes from the Western United States

Studies worldwide have shown that mercury (Hg) is a ubiquitous contaminant, reaching even the most remote environments such as high-altitude lakes via atmospheric pathways. However, very few studies have been conducted to assess Hg contamination levels of these systems. We sampled 90 mid-latitude, high-altitude lakes from seven national parks in the western United States during a four-week period in September 1999. In addition to the synoptic survey, routine monitoring and experimental studies were conducted at one of the lakes (Mills Lake) to quantify MeHg fluxrates and important process rates such as photo-demethylation. Results show that overall, high-altitude lakes have low total mercury (HgT) and methylmercury (MeHg) levels (1.07 and 0.05 ng L -1 , respectively), but a very good correlation of Hg to MeHg (r 2 = 0.82) suggests inorganic Hg(II) loading is a primary controlling factor of MeHg levels in dilute mountain lakes. Positive correlations were also observed for dissolved organic carbon (DOC) and both Hg and MeHg, although to a much lesser degree. Levels of MeHg were similar among the seven national parks, with the exception of Glacier National Park where lowerconcentrations were observed (0.02 ng L -1 ), and appear to be related to naturally elevated pH values there. Measured rates ofMeHg photo-degradation at Mills Lake were quite fast, and this process was of equal importance to sedimentation and stream flow for removing MeHg. Enhanced rates of photo-demethylation are likely an important reason why high-altitude lakes, with typically high water clarity and sunlight exposure, are low in MeHg.

California, Colorado, Montana, Wyoming