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At least 1,027 records · Page 57Linked to original sources

USGS1983

Helium isotopic variations in volcanic rocks from Loihi Seamount and the Island of Hawaii

Helium isotopic ratios ranging from 20 to 32 times the atmospheric 3He 4He(RA) have been observed in a suite of 15 basaltic glasses from the Loihi Seamount. These ratios, which are up to four times higher than those of MORB glasses and more than twice those of nearby Kilauea, are strongly suggestive of a primitive source of volatiles supplying this volcanism. The Loihi glasses measured span a broad compositional range, and the 3He/4He ratios were found to be generally lower for the alkali basalts than for the tholeiites. The component with a lower 3He 4He ratio appears to be associated with olivine xenocrysts, within which fluid inclusions are probably the carrier of contaminant helium. One Loihi sample has a much lower isotopic ratio (<5 RA), but a combination of low He concentration, high vesicularity, and presence of cracks lined with clay minerals suggests that the low ratio is due to gas loss and contamination by atmospheric helium. Crushing and melting experiments show that for modest vesicularities (<5% by volume) the Loihi glasses obey a MORB-type partitioning trend, but at higher vesicularities the data show considerably more scatter due to volatile mobilization. The high vesicularities, low extrusion pressure and generally low helium concentrations are consistent with a considerable degree of degassing. Analyses of dunites, plus a correlation between total helium concentrations with xenocryst abundances also suggest that xenocrysts are a significant carrier of contaminating (low 3He 4He) helium. 3He 4He ratios from samples of other Hawaiian volcanoes (Kilauea, Mauna Loa, Hualalai, and Mauna Kea) show a smooth decrease in 3He 4He with increasing volcano age and volume. We interpret this to be a synoptic picture of the time evolution of a hot-spot diapir: the earliest stage is characterized by primitive (> 30 RA) helium with some (variable) component of lithospheric contamination added during "breakthrough", while the later stages are characterized by a relaxation toward lithospheric 3He 4He ratios (??? 8 RA) due to isolation of the diapir from the mantle below (as the plate moves on), and subsequent mining of the inherited helium and contamination from the surrounding lithosphere. The abrupt contrast in 3He 4He ratios between Kilauea and Loihi, despite their close proximity, is indicative of the small lateral extent of the plume. ?? 1983.

Hawaii↗

USGS1983

Noble gas systematics for coexisting glass and olivine crystals in basalts and dunite xenoliths from Loihi Seamount

Noble gas isotopes including 3 He/ 4 He, 40 Ar/ 36 Ar and Xe isotope ratios were determined for coexisting glass and olivine crystals in tholeiitic and alkalic basalts and dunite xenoliths from Loihi Seamount. Glass and coexisting olivine crystals have similar 3 He/ 4 He ratios (2.8–3.4) × 10 −5 , 20 to 24 times the atmospheric ratio ( R A ), but different 40 Ar/ 36 Ar ratios (400–1000). Based on the results of noble gas isotope ratios and microscopic observation, some olivine crystals are xenocrysts. We conclude that He is equilibrated between glass and olivine xenocrysts, but Ar is not. The apparent high 3 He/ 4 He ratio (3 × 10 −5 ; = 21 R A ) coupled with a relatively high 40 Ar/ 36 Ar ratio (4200) for dunite xenoliths (KK 17-5) may be explained by equilibration of He between MORB-type cumulates and the host magma. Except for the dunite xenoliths, noble gas data for these Loihi samples are compatible with a model in which samples from hot spot areas may be explained by mixing between P (plume)-type and M (MORB)-type components with the addition of A (atmosphere)-type component. Excess 129 Xe has not been observed due to apparent large mass fractionation among Xe isotopes.

Earth and Planetary Science Letters↗

USGS1962

Behaviour of calcium carbonate in sea water

Anomalies in the behaviour of calcium carbonate in natural solutions diminish when considered in context. Best values found by traditional oceanographie methods for the apparent solubility product constant K ' CaCO 3 in sea water at atmospheric pressure are consistent mineralogically—at 36 parts per thousand salinity and T-25°C, K ' aragonlte is estimated as 1.12 × 10 −6 and K ' calcite as 0.61 × 10 −6 . At 30°C the corresponding values are 0.98 × 10 −6 for aragonite and 0.53 × 10 −6 for calcite. Because the K ' computations do not compensate for ionic activity, however, they cannot give thermodynamically satisfactory results. It is of interest, therefore, that approximate methods and information now available permit the estimation from the same basic data of an activity product constant K CaCO 3 close to that found in solutions to which Debye-Hückel theory applies. Such methods indicate approximate K aragonite 7.8 × 10 −9 for surface sea water at 29°C; K calcite would be proportionately lower. Field data and experimental results indicate that the mineralogy of precipitated CaCO 3 depends primarily on degree of supersaturation, thus also on kinetic or biologic factors that facilitate or inhibit a high degree of supersaturation. The shallow, generally hypersaline bank waters west of Andros Island yield aragonitic sediments with O 18 O 16 "> O18O16 ratios that imply precipitation mainly during the warmer months, when the combination of a high rate of evaporation, increasing salinity (and ionic strength), maximal temperatures and photosynthetic removal of CO 2 result in high apparent supersaturation. The usual precipitate from solutions of low ionic strength is calcite, except where the aragonite level of supersaturation is reached as a result of diffusion phenomena ( e.g. dripstones), gradual and marked evaporation, or biologic intervention. Published data also suggest the possibility of distinct chemical milieus for crystallographic variations in skeletal calcium carbonate. It appears that in nature aragonite precipitates from solutions that are supersaturated with respect to both calcite and aragonite and calcite between saturation levels for the two species. Such a relation is consistent with Ostwald's rule of successive reactions. Aragonitc of marine origin persists in contact with supersaturated interstitial solutions at ordinary temperature and pressure. Conversion to calcite follows transfer to solutions undersaturated with respect to aragonite or upon exposure to the moist atmosphere.

Geochimica et Cosmochimica Acta↗

USGS1993

Noble gases in submarine pillow basalt glasses from Loihi and Kilauea, Hawaii: A solar component in the Earth

Noble gas elemental and isotopic abundances have been analysed in twenty-two samples of basaltic glass dredged from the submarine flanks of two currently active Hawaiian volcanoes, Loihi Seamount and Kilauea. Neon isotopic ratios are enriched in 20 Ne and 21 Ne by as much as 16% with respect to atmospheric ratios. All the Hawaiian basalt glass samples show relatively high 3 He 4 He "> 3He4He ratios. The high 20 Ne 22 Ne "> 20 Ne 22 Ne values in some of the Hawaiian samples, together with correlations between neon and helium systematics, suggest the presence of a solar component in the source regions of the Hawaiian mantle plume. The solar hypothesis for the Earth's primordial noble gas composition can account for helium and neon isotopic ratios observed in basaltic glasses from both plume and spreading systems, in fluids in continental hydrothermal systems, in CO 2 well gases, and in ancient diamonds. These results provide new insights into the origin and evolution of the Earth's atmosphere.

Geochimica et Cosmochimica Acta↗

USGS1987

Large-scale volcano-ground ice interactions on Mars

The process of volcano-ground ice interaction on Mars is investigated by thermodynamic calculations and observations of Viking Orbiter images. We develop a numerical model of volcano-ground ice interaction that includes heat transport by conduction, radiation from the surface, heat transfer to the atmosphere, and H 2 O phase changes in an ice-rich permafrost. We consider eruption of lava flows over permafrost, and intrusion of sills into permafrost. For eruption of lava over permafrost, most of the heat in the flow is lost by radiation and atmospheric effects. The amount of H 2 O liquid and vapor produced is small, and its removal would not be sufficient to cause collapse that would lower the surface of the lava flow below the surrounding terrain. For intrusion of a sill, most of the heat in the sill eventually goes into H 2 O phase changes, producing much larger amounts of water that could have profound geomorphic and geochemical effects. Approximate meltwater discharge rates are calculated for both extrusive and intrusive interactions. We examine two large regions of large-scale volcano-ground ice interactions. Near Aeolis Mensae, intrusion of a complex of dikes and sills into ice-rich ground has produced substantial melting, with mobilization and flow of material. This interaction probably also produced large quantities of palagonite tuff and breccia. Morphologic evidence for progressive fluidization implies that meltwater was stored beneath the surface for some time, and that most of the release of water and volcanic mudflow took place late in the interaction. Northeast of Hellas, several large channels emanate from the area near the volcano Hadriaca Patera. If genetically related to the volcanic activity, large collapse features at the sources of some channels must have originated due to heat from large buried magma bodies. A channel emerging directly from the base of Hadriaca Patera may have originated from release of heat from thick extruded material. Other small channels in the region results from heat released from surface lava flows. Inferred channel discharges may be compared to discharge rates calculated for lava-ground ice interactions. Such comparisons show that meltwater probably accumulated beneath the surface and then was released rapidly, with a discharge rate limited by soil permeability. Volcano-ground ice interaction has been a widespread and important geologic process on Mars, and may be the primary source of palagonites making up the ubiquitous Martian dust.

Icarus↗

USGS1984

Experimental studies in natural groundwater recharge dynamics: Assessment of recent advances in instrumentation

To quantify and model the natural groundwater-recharge process, two sites in south-central Kansas, U.S.A., were instrumented with various modern sensors and data microloggers. The atmospheric-boundary layer and the unsaturated and saturated soil zones were monitored as a unified regime. Data from the various sensors were collected using microloggers in combination with magnetic-cassette tape, graphical and digital recorders, analog paper-tape recorders, and direct observations to evaluate and automate data collection and processing. Atmospheric sensors included an anemometer, a tipping-bucket raingage, an air-temperature thermistor, a relative-humidity probe, a net radiometer, and a barometric-pressure transducer. Sensors in the unsaturated zone consisted of soil-temperature thermocouples, tensiometers coupled with pressure transducers and dial gages, gypsum blocks, and a neutron moisture probe operated by an observer. The saturated-zone sensors consisted of a water-level pressure transducer, a conventional float gage connected to a variable potentiometer, soil thermocouples, and a number of multiple-depth piezometers. Evaluation of the operation of these sensors and recorders indicated that certain types of equipment such as pressure transducers are very sensitive to environmental conditions. Extraordinary steps had to be taken to protect some of the equipment, whereas other equipment seemed to be reliable under all conditions. Based on such experiences, a number of suggestions aimed at improving such investigations are outlined.

Kansas↗

USGS1986

Determination of the components of stormflow using water chemistry and environmental isotopes, Mattole River basin, California

The chemical and isotopic composition of rainfall and stream water was monitored during a storm in the Mattole River basin of northwestern California. About 250 mm of rain fell during 6 days (∼80% within a 42 h period) in late January, 1972, following 24 days of little or no precipitation. River discharge near Petrolia increased from 22 m 3 s −1 to a maximum of 1300 m 3 s −1 while chloride and silica concentrations decreased only from 3.2 to 2.1 and 11.5 to 8.6 mgl −1 , respectively. Meanwhile, the isotopic composition of the river changed from δD = -42%, δ 18 O = -6.8% and 40 tritium units (T.U.) to extreme values at highest flow of δD = -35%, δ 18 O = -5.9% and 25 T.U. in response to volume-weighted rainfall averaging δD = -19.5%, δ 18 O = -3.1% and 18 T.U. Despite much rainfall of a composition quite different from that of the prestorm river water, “buffering” processes in the watershed greatly restricted changes in the chemical and isotopic content of the river during storm runoff. Because of the physical and hydrologic characteristics of the watershed, major contributions of groundwater to stormflow are very unlikely. The large increase in dissolved chemical load observed at maximum river discharge required that extensive interaction with, and presumably penetration of, soils occurred within a few hours time. Such a large increase in chemical load also required subsurface stormflow throughout a high proportion of the watershed. Chemical and isotopic stabilization of stormflow is believed to be due mainly to displacement of prestorm soil water, with some effects on river chemistry due to rapid rain-soil interactions. The isotopic and chemical composition of prestorm soil moisture cannot readily be predicted a priori because of possible variability in rainfall composition, evaporation, and exchange with atmospheric moisture, nor can it be assumed that baseflow has a predictable relation to the chemical or isotopic composition of water displaced from soils during storms. Therefore, it seems inappropriate to draw conclusions as to the relative proportions of groundwater and rainfall in runoff from a particular storm based only on the average compositions of rainfall, stormflow, and prestorm river water, as has been done in most previous isotope hydrograph studies. Given the great variation in hydrology, topography, soil characteristics, rainfall intensity and quantity, etc. from place to place, the relative amount of overland flow, subsurface flow from the unsaturated zone and of groundwater in stormflow can vary greatly in time and space.

California↗

USGS1992

Spectral ratio method for measuring emissivity

The spectral ratio method is based on the concept that although the spectral radiances are very sensitive to small changes in temperature the ratios are not. Only an approximate estimate of temperature is required thus, for example, we can determine the emissivity ratio to an accuracy of 1% with a temperature estimate that is only accurate to 12.5 K. Selecting the maximum value of the channel brightness temperatures is an unbiased estimate. Laboratory and field spectral data are easily converted into spectral ratio plots. The ratio method is limited by system signal:noise and spectral band-width. The images can appear quite noisy because ratios enhance high frequencies and may require spatial filtering. Atmospheric effects tend to rescale the ratios and require using an atmospheric model or a calibration site.

Colorado↗

USGS1986

An analytical scheme for determining forms of sulphur in oil shales and associated rocks

An analytical scheme for determining various forms of sulphur in oil shales and associated rocks is presented. Acid-soluble sulphate, sulphur contained in monosulphide and in disulphide minerals, and organically-bound sulphur are all quantitatively recovered as separate fractions. Finely-ground oil-shale samples are treated in an inert atmosphere with 6 M hydrochloric acid to dissolve the acid-soluble sulphate minerals and form H 2 S from the decomposition of monosulphide minerals. The acid-soluble sulphate is precipitated as barium sulphate and the H 2 S is collected and weighed as silver sulphide. Disulphide minerals in the solid residue from the acid treatment are reduced by an acidified Cr(II) solution in an inert atmosphere, releasing the sulphide as H 2 S. The H 2 S is collected as silver sulphide. An Eschka fusion oxidizes and solubilizes all sulphur remaining within the Cr(II)-treated residue. This sulphate represents organically-bound sulphur and is collected as barium sulphate. The analytical procedures have been verified by using 57 Fe Mössbauer spectroscopy. Good agreement between the chemical and Mössbauer data substantiated the sequential removal of the forms of sulphur and also demonstrated the ability of Mössbauer spectroscopy to determine the absolute quantities of iron present in specific minerals.

Talanta↗

USGS1985

Validation of an automated fluorescein method for determining bromide in water

Surface, atmospheric precipitation and deionized water samples were spiked with ??g l-1 concentrations of bromide, and the solutions stored in polyethylene and polytetrafluoroethylene bottles. Bromide was determined periodically for 30 days. Automated fluorescein and ion chromatography methods were used to determine bromide in these prepared samples. Analysis of the data by the paired t-test indicates that the two methods are not significantly different at a probability of 95% for samples containing from 0.015 to 0.5 mg l-1 of bromide. The correlation coefficient for the same sets of paired data is 0.9987. Recovery data, except for the surface water samples to which 0.005 mg l-1 of bromide was added, range from 89 to 112%. There appears to be no loss of bromide from solution in either type of container.Surface, atmospheric precipitation and deionized water samples were spiked with mu g l** minus **1 concentrations of bromide, and the solutions stored in polyethylene and polytetrafluoroethylene bottles. Bromide was determined periodically for 30 days. Automated fluorescein and ion chromatography methods were used to determine bromide in these prepared samples. Analysis of the data by the paired t-test indicates that the two methods are not significantly different at a probability of 95% for samples containing from 0. 015 to 0. 5 mg l** minus **1 of bromide. The correlation coefficient for the same sets of paired data is 0. 9987. Recovery data, except for the surface water samples to which 0. 005 mg l** minus **1 of bromide was added, range from 89 to 112%. Refs.

Water Research↗

USGS1994

Interactive effects of CO2 enrichment and temperature on the growth of dioecious Hydrilla verticillata

Experiments of plant growth responses to different CO 2 concentrations and temperatures were conducted in growth chambers to explore the interactive effects of atmospheric CO 2 enrichment and temperature on the growth and dry matter allocation of dioecious Hydrilla [Hydrilla verticillata (L.f.) Royle]. Hydrilla plants were exposed to two atmospheric CO 2 concentrations (350 and 700 ppm) and three temperatures (15, 25 and 32°C) under a 12-hr photoperiod for about 2 months. The plant growth analysis showed that elevated CO 2 appeared to enhance the growth of Hydrilla , and that the percentage of the enhancement is strongly temperature-dependent. Maximum biomass production was achieved at 700 ppm CO 2 and 32°C. At 15°C, the total dry matter production was increased about 27% by doubling CO 2 , due to a 26% enhancement of leaf biomass, a 34% enhancement of stem biomass and 16% enhancement of root biomass. At 25°C, the dry matter production was increased about 46% by doubling CO 2 , due to a 29% enhancement of leaf biomass, a 27% enhancement of stem biomass and 40% enhancement of root biomass. At 32°C, however, the percentage of the enhancement of total dry matter production by doubling CO 2 was only about 7%. The dry matter allocation among different plant parts was influenced by temperature but not by elevated CO 2 concentration.

Environmental and Experimental Botany↗

USGS1993

SEM-EDX and isotope characterization of the organic sulfur in macerals and chars in Illinois Basin coals

Two samples of the Herrin (Illinois No. 6) Coal and one sample of the Colchester (Illinois No. 2) Coal from the Illinois Basin were studied to evaluate the spatial distribution of organic sulfur within macerals occurring next to pyrite grains, both in the raw coal and their chars. The chars were produced by pyrolysing the coal at 250–550°C in a nitrogen atmosphere. Representative splits of the coals and their chars were mounted in epoxy and polished for optical microscopy and scanning electron microscopy-energy dispersive x-ray spectroscopy (SEM-EDX). Determinations of organic sulfur concentrations were made at 996 locations within macerals, mostly vitrinite, around 115 grains of pyrite and at 50 locations around 5 pores in chars. The pyrite considered here is restricted to the disseminated type within macerals. On the average, the organic sulfur content increased near pyrite grains after the coals were charred at 550°C, indicating that some of the pyritic sulfur released during charring was retained within the organic matrix rather than being emitted to the atmosphere. One of the coal samples and its chars were isotopically characterized by chemically separating the pyritic and organic sulfur fractions, followed by analyzing the isotopes of the sulfur forms with a Nuclide 6–60 ratio mass spectrometer. The sulfur isotope (δ 34 S) data confirmed the movement of pyritic sulfur into the macerals after charring to 550°C. About 18% of the organic sulfur that remained in the 550°C char had originally been pyritic sulfur in the untreated coal.

Organic Geochemistry↗

USGS1995

A Lagrangian stochastic model for aerial spray transport above an oak forest

An aerial spray droplets' transport model has been developed by applying recent advances in Lagrangian stochastic simulation of heavy particles. A two-dimensional Lagrangian stochastic model was adopted to simulate the spray droplet dispersion in atmospheric turbulence by adjusting the Lagrangian integral time scale along the drop trajectory. The other major physical processes affecting the transport of spray droplets above a forest canopy, the aircraft wingtip vortices and the droplet evaporation, were also included in each time step of the droplets' transport. The model was evaluated using data from an aerial spray field experiment. In generally neutral stability conditions, the accuracy of the model predictions varied from run-to-run as expected. The average root-mean-square error was 24.61 IU cm −2 , and the average relative error was 15%. The model prediction was adequate in two-dimensional steady wind conditions, but was less accurate in variable wind condition. The results indicated that the model can simulate successfully the ensemble; average transport of aerial spray droplets under neutral, steady atmospheric wind conditions.

Agricultural and Forest Meteorology↗

USGS1996

Variability in surface energy flux partitioning during Washita '92: Resulting effects on Penman-Monteith and Priestley-Taylor parameters

During the Washita '92 field experiment, the local surface energy balance was evaluated at four locations in the USDA-ARS Little Washita River Watershed near Chickasha, OK, using the Bowen ratio-energy balance (BREB) approach. For any given day, differences in the partitioning of the available energy appeared to be mostly a function of the type of vegetation at the site, while the actual magnitude of the fluxes was mostly affected by cloud cover. The soil surface was initially wet, and gradually dried during the field experiment. However, there was not a corresponding decrease in the evaporative fraction, which would have indicated a decreasing contribution of soil evaporation to the total latent heat flux. Ground weather data indicated a large shift in the direction and magnitude of the surface winds, and a significant increase in air temperature and vapor pressure deficit. During this period, the evaporative fraction actually increased at two of the four sites. The response of the different sites to the changing near-surface atmospheric conditions was studied in more detail by evaluating the canopy resistance ( r c ) to evaporation using the Penman-Monteith equation and the Priestley-Taylor parameter (α). Midday averages of ( r c ) and (α) tended to decrease (increase) with increasing vapor pressure deficit for two of the sites while such a trend was not evident for the other two sites. Estimates of stomatal resistances indicated that significant plant physiological differences existed between the sites containing weedy vegetation versus the grasses at the pasture/rangeland sites. Even though soil moisture conditions were relatively wet, a was less than 1 at all sites and there was no trend in α as a function of surface soil moisture conditions. These findings suggest that vegetation types C in mixed agricultural /rangeland ecosystems can have significantly different responses to similar atmospheric forcing conditions.

Agricultural and Forest Meteorology↗

USGS1995

Effects of a 2 x CO2 climate on two large lake systems: Pyramid Lake, Nevada, and Yellowstone Lake, Wyoming

The possible effects of trace-gas induced climatic changes on Pyramid and Yellowstone Lakes are assessed using a model of lake temperature. The model is driven by 3 1 2 "> 312 years of hourly meteorological data obtained directly from the output of double-CO 2 experiments (2 × CO 2 ) conducted with a regional climate model nested in a general circulation model. The regional atmospheric model is the climate version of the National Center for Atmospheric Research/Pennsylvania State University mesoscale model, MM4. Average annual surface temperature of Pyramid Lake for the 2 × CO 2 climate is 15.5 ± 5.4°C (±1 σ), 2.8°C higher than the control. Annual overturn of the lake ceases as a result of these higher temperatures for the 2 × CO 2 climate. Evaporation increases from 1400 mm yr −1 in the control to 1595 mm yr −1 in the 2 × CO 2 simulation, but net water supplied to the Pyramid Lake basin increases from −6 mm yr −1 in the control to +27 mm yr −1 in the 2 × CO 2 simulation due to increased precipitation. For the open water periods, the average annual surface temperature of Yellowstone Lake is 13.2 ± 5.1°C for the 2 × CO 2 climate, a temperature 1.6°C higher than the control. The annual duration of ice cover on the lake is 152 days in the 2 × CO 2 simulation, a reduction of 44 days relative to the control. Warming of the lake for the 2 × CO 2 climate is mostly confined to the near-surface. Simulated spring overturn for the 2 × CO 2 climate occurs earlier in the year and fall overturn later than in the control. Evaporation increases from 544 mm yr −1 to 600 mm yr −1 in the 2 × CO 2 simulation, but net water supplied to the Yellowstone Lake basin increases from +373 mm yr −1 in the control to +619 mm yr −1 due to increased precipitation. The effects of these climatic changes suggest possible deterioration of water quality and productivity in Pyramid Lake and possible enhancement of productivity in Yellowstone Lake.

Nevada, Wyoming↗

USGS2010

Climate warming-induced intensification of the hydrologic cycle: A review of the published record and assessment of the potential impacts on agriculture

Climate warming is expected to intensify and accelerate the global hydrologic cycle resulting in increases in evaporation, evapotranspiration (ET), atmospheric water-vapor content, and precipitation. The strength of the hydrologic response, or sensitivity of the response for a given degree of warming, is a critical outstanding question in climatology and hydrology. In this review chapter, I examine the published record of trends in various components of the hydrologic cycle and associated variables to assess observed hydrologic responses to warming during the period of observational records. Global and regional trends in evaporation, ET, and atmospheric water-vapor content and several large river basin water-balance studies support an ongoing intensification of the hydrologic cycle. Global trends in precipitation, runoff, and soil moisture are more uncertain than the trends in the variables noted above, in part because of high spatial and temporal variability. Trends in associated variables, such as systematic changes in ocean salinity, the length of the growing season, and the rate of precipitation recycling are generally consistent with intensification of the hydrologic cycle. The evidence for an increase in the frequency, intensity, or duration of extreme-weather events like hurricanes is mixed and remains uncertain. The largest potential impacts to agricultural systems depend greatly on the responses of hydrologic variables that are the most uncertain; for example, intensity and duration of heavy rainfall events; frequency, intensity, and duration of major storms and droughts; and rates of erosion. Impacts on agriculture will depend greatly on how insects, diseases, weeds, nutrient cycling, effectiveness of agrichemicals, and heat stress are affected by an intensification of the hydrologic cycle.

Advances in Agronomy↗

USGS2009

Aeromicrobiology/air quality

The most prevalent microorganisms, viruses, bacteria, and fungi, are introduced into the atmosphere from many anthropogenic sources such as agricultural, industrial and urban activities, termed microbial air pollution (MAP), and natural sources. These include soil, vegetation, and ocean surfaces that have been disturbed by atmospheric turbulence. The airborne concentrations range from nil to great numbers and change as functions of time of day, season, location, and upwind sources. While airborne, they may settle out immediately or be transported great distances. Further, most viable airborne cells can be rendered nonviable due to temperature effects, dehydration or rehydration, UV radiation, and/or air pollution effects. Mathematical microbial survival models that simulate these effects have been developed.

Book chapter↗

USGS2018

Shrubland carbon sink depends upon winter water availability in the warm deserts of North America

Global-scale studies suggest that dryland ecosystems dominate an increasing trend in the magnitude and interannual variability of the land CO 2 sink. However, such model-based analyses are poorly constrained by measured CO 2 exchange in open shrublands, which is the most common global land cover type, covering ∼14% of Earth’s surface. Here we evaluate how the amount and seasonal timing of water availability regulate CO 2 exchange between shrublands and the atmosphere. We use eddy covariance data from six US sites across the three warm deserts of North America with observed ranges in annual precipitation of ∼100–400mm, annual temperatures of 13–18°C, and records of 2–8 years (33 site-years in total). The Chihuahuan, Sonoran and Mojave Deserts present gradients in both mean annual precipitation and its seasonal distribution between the wet-winter Mojave Desert and the wet-summer Chihuahuan Desert. We found that due to hydrologic losses during the wettest summers in the Sonoran and Chihuahuan Deserts, evapotranspiration (ET) was a better metric than precipitation of water available to drive dryland CO 2 exchange. In contrast with recent synthesis studies across diverse dryland biomes, we found that NEP could not be directly predicted from ET due to wintertime decoupling of the relationship between ecosystem respiration (R eco ) and gross ecosystem productivity (GEP). Ecosystem water use efficiency (WUE=GEP/ET) did not differ between winter and summer. Carbon use efficiency (CUE=NEP/GEP), however, was greater in winter because R eco returned a smaller fraction of carbon to the atmosphere (23% of GEP) than in summer (77%). Combining the water-carbon relations found here with historical precipitation since 1980, we estimate that lower average winter precipitation during the 21st century reduced the net carbon sink of the three deserts by an average of 6.8TgC yr 1 . Our results highlight that winter precipitation is critical to the annual carbon balance of these warm desert shrublands.

Agricultural and Forest Meteorology↗