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High-pressure deformation of calcite marble and its transformation to aragonite under non-hydrostatic conditions

We conducted deformation experiments on Carrara marble in the aragonite and calcite stability fields to observe the synkinematic transformation of calcite to aragonite, and to identify any relationships between transformation and deformation or sample strength. Deformation-induced microstructures in calcite crystals varied most significantly with temperature, ranging from limited slip and twinning at 400°C, limited recrystallization at 500°C, widespread recrystallization at 600 and 700°C, to grain growth at 800–900°C. Variations in confining pressure from 0.3 to 2.0 GPa have no apparent effect on calcite deformation microstructures. Aragonite grew in 10 −6 -10 −7 s −1 strain rate tests conducted for 18–524 h at confining pressures of 1.7–2.0 GPa and temperatures of 500–600°C. As in our previously reported hydrostatic experiments on this same transformation, the aragonite nucleated on calcite grain boundaries. The extent of transformation varied from a few percent conversion near pistons at 400°C, 2.0 GPa and 10 −4 s −1 strain rate in a 0.8 h long experiment, to 98% transformation in a 21-day test at a strain rate of 10 −7 s −7 , a temperature of 600°C and a pressure of 2.0 GPa. At 500°C, porphyroblastic 100–200 μm aragonite crystals grew at a rate faster than 8 × 10 −1 m s −1 . At 600°C, the growth of aragonite neoblasts was slower, ≈6 × 10 −1 m s −1 , and formed ‘glove-and-finger’ cellularprecipitation-like textures identical to those observed in hydrostatic experiments. The transformation to aragonite is not accompanied by a shear instability or anisotropic aragonite growth, consistent with its relatively small volume change and latent heat in comparison with compounds that do display those features.

Journal of Structural Geology↗

Radiometric dating of quaternary deposits and the hominid mandible of Lake Banyolas, Spain

We report results of U-series analyses of the travertine matrix surrounding the Banyolas mandible that indicate an age of 45??4 ka bp. The mandible, an archaic hominid fossil generally deemed of mid-Pleistocene age, was recovered from a travertine matrix in 1887. Similar analyses on 21 travertine samples from quarries near the discovery site yield coherent U-series dates in correct stratigraphic order, ranging from 44 ka bp to 117 ka bp. Isotopic composition of these samples and the mandible matrix show no evidence of open system behaviour. Coherent isotopic results from adjacent quarries support the validity of the date on the mandible travertine, and we conclude the mandible is much younger than previously believed. ?? 1991.

Catalonia↗

Radioactive springs geochemical data related to uranium exploration

Radioactive mineral springs and wells at 33 localities in the States of Colorado, Utah, Arizona and New Mexico in the United States were sampled and studied to obtain geochemical data which might be used for U exploration. The major source of radioactivity at mineral spring sites is 226 Ra. Minor amounts of 228 Ra, 238 U and 232 Th are also present. Ra is presumed to have been selectively removed from possibly quite deep uranium-mineralized rock by hydrothermal solutions and is either precipitated at the surface or added to fresh surface water. In this way, the source rocks influence the geochemistry of the spring waters and precipitates. Characteristics of the spring waters at or near the surface are also affected by variations in total dissolved solids, alkalinity, temperature and co-precipitation. Spring precipitates, both hard and soft, consist of four major types: (1) calcite travertine; (2) iron- and arsenic-rich precipitates; (3) manganese- and barium-rich precipitates; and (4) barite, in some instances accompanied by S, Ra and U, if present in the spring water, are co-precipitated with the barite, Mn-Ba and Fe-As precipitates. Using parameters based on U and Ra concentrations in waters and precipitates springsite areas are tentatively rated for favourability as potential uraniferous areas.

Journal of Geochemical Exploration↗

A rapid, partial leach and organic separation for the sensitive determination of Ag, Bi, Cd, Cu, Mo, Pb, Sb, and Zn in surface geologic materials by flame atomic absorption

A solution of dilute hydrochloric acid, ascorbic acid, and potassium iodide has been found to dissolve weakly bound metals in soils, stream sediments, and oxidized rocks. Silver, Bi, Cd, Cu, Mo, Pb, Sb, and Zn are selectively extracted from this solution by a mixture of Aliquat 336 (tricaprylyl methyl ammonium chloride) and MIBK (methyl isobutyl ketone). Because potentially interfering major and minor elements do not extract, the organic separation allows interference-free determinations of Ag and Cd to the 0.05 ppm level, Mo, Cu, and Zn to 0.5 ppm, and Bi, Pb, and Sb to 1 ppm in the sample using flame atomic absorption spectroscopy. The analytical absorbance values of the organic solution used in the proposed method are generally enhanced more than threefold as compared to aqueous solutions, due to more efficient atomization and burning characteristics. The leaching and extraction procedures are extremely rapid; as many as 100 samples may be analyzed per day, yielding 800 determinations, and the technique is adaptable to field use. The proposed method was compared to total digestion methods for geochemical reference samples as well as soils and stream sediments from mineralized and unmineralized areas. The partial leach showed better anomaly contrasts than did total digestions. Because the proposed method is very rapid and is sensitive to pathfinder elements for several types of ore deposits, it should be useful for reconnaissance surveys for concealed deposits.

Journal of Geochemical Exploration↗

The effect of scale on the interpretation of geochemical anomalies

The purpose of geochemical surveys changes with scale. Regional surveys identify areas where mineral deposits are most likely to occur, whereas intermediate surveys identify and prioritize specific targets. At detailed scales specific deposit models may be applied and deposits delineated. The interpretation of regional geochemical surveys must take into account scale-dependent difference in the nature and objectives of this type of survey. Overinterpretation of regional data should be resisted, as should recommendations to restrict intermediate or detailed follow-up surveys to the search for specific deposit types or to a too limited suite of elements. Regional surveys identify metallogenic provinces within which a variety of deposit types and metals are most likely to be found. At intermediate scale, these regional provinces often dissipate into discrete clusters of anomalous areas. At detailed scale, individual anomalous areas reflect local conditions of mineralization and may seem unrelated to each other. Four examples from arid environments illustrate the dramatic change in patterns of anomalies between regional and more detailed surveys.

Journal of Geochemical Exploration↗

Leachability of uranium and other elements from freshly erupted volcanic ash

A study of leaching of freshly erupted basaltic and dacitic air-fall ash and bomb fragment samples, unaffected by rain, shows that glass dissolution is the dominant process by which uranium is initially mobilized from air-fall volcanic ash. Si, Li, and V are also preferentially mobilized by glass dissolution. Gaseous transfer followed by fixation of soluble uranium species on volcanic-ash particles is not an important process affecting uranium mobility. Gaseous transfer, however, may be important in forming water-soluble phases, adsorbed to ash surfaces, enriched in the economically and environmentally important elements Zn, Cu, Cd, Pb, B, F, and Ba. Quick removal of these adsorbed elements by the first exposure of freshly erupted ash to rain and surface water may pose short-term hazards to certain forms of aquatic and terrestrial life. Such rapid release of material may also represent the first step in transportation of economically important elements to environments favorable for precipitation into deposits of commercial interest. Ash samples collected from the active Guatemalan volcanoes Fuego and Pacaya (high-Al basalts) and Santiaguito (hornblende-hypersthene dacite); bomb fragments from Augustine volcano (andesite-dacite), Alaska, and Heimaey (basalt), Vestmann Islands, Iceland; and fragments of "rhyolitic" pumice from various historic eruptions were subjected to three successive leaches with a constant water-to-ash weight ratio of 4:1. The volcanic material was successively leached by: (1) distilled-deionized water (pH = 5.0-5.5) at room temperature for 24 h, which removes water-soluble gases and salts adsorbed on ash surfaces during eruption; (2) dilute HCl solution (pH = 3.5-4.0) at room temperature for 24 h, which continues the attack initiated by the water and also attacks acid-soluble sulfides and oxides; (3) a solution 0.05 M in both Na,CO, and NaHCO, (pH = 9.9) at 80°C for one week, which preferentially dissolves volcanic glass. The first two leaches mimic interaction of ash with rain produced in the vicinity of an active eruption. The third leach accelerates the effect of prolonged contact of volcanic ash with alkaline ground water present during ash diagenesis.

Journal of Volcanology and Geothermal Research↗

Comparison of hydrothermal alteration of carboniferous carbonate and siliclastic rocks in the Valles caldera with outcrops from the Socorro caldera, New Mexico

Continental Scientific Drilling Program (CSDP) drill hole VC-2B [total depth 1761.7 m (5780 ft); maximum temperature 295 °C] was continuously cored through the Sulphur Springs hydrothermal system in the western ring-fracture zone of the 1.14 Ma Valles caldera. Among other units, the hole penetrated 760.2 m (2494.1 ft) of Paleozoic carbonate and siliciclastic strata underlying caldera fill and precaldera volcanic and epiclastic rocks. Comparison of the VC-2B Paleozoic rocks with corresponding lithologies within and around the 32.1 Ma Socorro caldera, 192 km ( 119 miles) to the south-southwest, provides insight into the variability of alteration responses to similar caldera-related hydrothermal regimes. The Pennsylvanian Madera Limestone and Sandia Formation from VC-2B preserve many of the sedimentological and diagenetic features observed in these units on a regional basis and where unaffected by high temperatures or hydrothermal activity. Micrites in these formations in VC-2B are generally altered and mineralized only where fractured or brecciated, that is, where hydrothermal solutions could invade carbonate rocks which were otherwise essentially impermeable. Alteration intensity (and correspondingly inferred paleopermeability) is only slightly higher in carbonate packstones and grainstones, low to intermediate in siltstones and claystones, and high in poorly cemented sandstones. Hydrothermal fracture-filling phases in these rocks comprise sericite (and phengite), chlorite, allanite, apatite, an unidentified zeolite and sphene in various combinations, locally with sphalerite, galena, pyrite and chalcopyrite. Terrigenous feldspars and clays are commonly altered to chlorite and seriate, and euhedral anhydrite “porphyroblasts” with minor chlorite occur in Sandia Formation siltstone. Fossils are typically unaltered, but the walls of some colonial bryozoans in the Madera Limestone are altered to the assemblage chlorite-sericite-epidote-allanite. La, Ce and Nd are present in an unidentified hydrothermal mineral occurring throughout much of the VC-2B Pennsylvanian sequence. Carboniferous carbonate and siliciclastic formations within and around the Socorro caldera show a similar style of alteration and mineralization to their Valles caldera counterparts, but by contrast locally host commercial, caldera-related, base-metal sulfide deposits. As in the Valles rocks, mineralization and alteration in those of the Socorro caldera were strongly controlled by porosity. Unless disrupted by fractures, breccias, or karst cavities ( not identified in Valles caldera drill holes), the rocks remained relatively unaltered. Where these features allowed ingress of mineralizing hydrothermal solutions, base-metal sulfides and rare-earth-element-bearing minerals were precipitated.

New Mexico↗

Mineral matter and potentially hazardous trace elements in coals from Qianxi Fault Depression Area in southwestern Guizhou, China

Mineralogy, coal chemistry and 21 potentially hazardous trace elements (PHTEs) of 44 coal samples from the Qianxi Fault Depression Area (QFDA) in southwestern Guizhou province, China have been systematically studied. The major minerals in coals studied are quartz, kaolinite, illite, pyrite, calcite, smectite, marcasite and accessory minerals, including rutile, dolomite, siderite, gypsum, chlorite, melanterite, apatite, collophane and florencite. The SiO2 content shows a broad variation (0.8-30.7%). A high SiO2 content in Late Permian coals reflects their enrichment in quartz. The Al2O3 content varies from 0.8% to 13.4%, Fe2O3 from 0.2% to 14.6%, CaO from <0.1% to 11.9% and the contents of other oxides are relatively low. The relationship between the major oxides and the ash content of coals from high to low is in the order of Si>Al>K>Ti>Na>Mg>Ca>Fe>S. A comparison with World coal averages shows that the Late Permian coals in QFDA are highly enriched in As, Hg, F and U, and are slightly enriched in Mo, Se, Th, V and Zn. The Late Triassic coals in QFDA are highly enriched in As and Hg, and are slightly enriched in Mo, Th and U. The concentrations of As, Hg, Mo, Se, Tl and Zn in the QFDA coal are higher than other Guizhou coal and Liupanshui coal nearby. The QFDA is an area strongly affected by the low-temperature hydrothermal activity during its geologic history (Yanshanian Age, about 189 Ma). The coals in QFDA are enriched in volatile PHTEs, including As, Hg, Se, Sb, Mo, among others. The regions where the coals are enriched in As, Hg and F have been mapped. The regions of coals enriched in volatile PHTEs overlap with the regions of noble metal ore deposits. These coals are located in the cores of anticline and anticlinorium, which are connected with the profound faults through the normal faults. Coals are enriched in volatile PHTEs as a result of the low-temperature hydrothermal activity associated with tectonic faulting. ?? 2003 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Functional group and individual maceral chemistry of high volatile bituminous coals from southern Indiana: Controls on coking

The individual maceral chemistries of two Pennsylvanian, high volatile bituminous coals, the Danville Coal Member (Dugger Formation, R o=0.55%) and the Lower Block Coal Member (Brazil Formation, R o=0.56%) of Indiana, were investigated using electron microprobe and Fourier Transform Infrared Spectrometry (FTIR) techniques, with the purpose of understanding differences in their coking behavior. Microprobe results reveal that carbon contents are highest in inertinite and sporinite, followed by desmocollinite and telocollinite. Oxygen and organic nitrogen are most abundant in telocollinite and desmocollinite; sporinite and inertinite contain lesser amounts of these two elements. Organic sulfur contents are highest in sporinite, lowest in inertinite, and intermediate in desmocollinite and telocollinite. Vitrinites within the Danville and Lower Block coals are very similar in elemental composition, while Lower Block inertinites and sporinites have higher carbon, lower oxygen, and sulfur contents which, when combined with the inertinite-and sporinite-rich composition of the Lower Block seam, strongly influences its whole coal chemistry. Fourier transform infrared spectrometry revealed greater aromatic hydrogen in the Lower Block coal, along with higher CH2/CH3 ratios, which suggest that liptinites contribute considerable amounts of long-chain, unbranched aliphatics to the overall kerogen composition of the Lower Block coal. Long-chain, unbranched aliphatics crack at higher temperatures, producing tar and oily byproducts during coking; these may help increase Lower Block plasticity. Electron microprobe and FTIR results indicate that individual maceral chemistries, combined with the maceral composition of the seam, are the primary control of better coking properties of the Lower Block coal. ?? 2003 Elsevier B.V. All rights reserved.

International Journal of Coal Geology↗

Petrology and chemistry of Permian coals from the Paraná Basin: 1. Santa Terezinha, Leão-Butiá and Candiota Coalfields, Rio Grande do Sul, Brazil

The current paper presents results on petrological and geochemical coal seam characterization in Permian coal-bearing strata from the Paran&aacute; Basin, southern Brazil. Sequence stratigraphic analysis shows that peat accumulation in Permian time was closely linked to transgressive/regressive cycles, with peat accumulation occurring in a predominantly back barrier/lagoonal setting. Coal petrographic analysis indicates subbituminous coals at Candiota and Le&atilde;o-Buti&aacute; and high volatile bituminous coals at Santa Terezinha, where locally the coal seams are thermally altered by volcanic intrusions. Petrographic composition is highly variable, with seams at Candiota and Santa Terezinha frequently enriched in inertinite. Chemical analyses indicate that all coals are mineral matter-rich (mean 49.09 wt.%), with SiO 2 and Al 2 O 3 dominating as determined by ICP-AES. Quartz is also the predominant mineral detected by X-ray diffraction, where it is associated with feldspar, kaolinite and hematite and iron-rich carbonates. The results from Scanning Electron Microscopy are broadly consistent with the bulk chemical and mineralogical analysis. Quartz and clays are common in all samples analyzed. Other minerals observed were, amongst others, carbonates (calcite, siderite, ankerite), pyrite, monazite, kaolinite, barite, sphalerite, rutile and quartz of volcanic origin. The distribution of trace elements is well within the range typical for coal basins of other areas despite the fact that the Paran&aacute; Basin coals are very high in ash yields. The average concentrations for elements of environmental concern (As, B, Be, Cd, Co, Cr, Cu, Hg, Li, Mn, Mo, Ni, Pb, Sb, Se, Tl, U, V, Zn) are similar to or less than the mean values for U.S. coal. However, considered on an equal energy basis, Paran&aacute; Basin coals will produce in combustion 5 to 10 times the amount of most elements compared to an equal weight US coal. Concentrations of major and trace elements, such as Fe, B and S, appear to be controlled by depositional setting, with increasing values in coal seams overlain by brackish/marine strata. Hierarchical cluster analysis identified three groups of major minerals and seven groups of trace elements based on similarity levels. On a regional scale, the coalfields can be separated by the differences in rank (Candiota and Le&atilde;o-Buti&aacute; versus Santa Terezinha) and by applying discriminant analysis based on 4 trace elements (Li, As, Sr, Sb). Highest Rb and Sr values occur at Candiota and are linked to syngenetic volcanism of the area, whereas high Y and Sr values at Santa Terezinha can be related to the frequent diabase intrusions in that area.

International Journal of Coal Geology↗

Coal lithotypes before and after saturation with CO2; insights from micro- and mesoporosity, fluidity, and functional group distribution

Four lithotypes, vitrain, bright clarain, clarain, and fusain, were hand-picked from the core of the Pennsylvanian Springfield Coal Member (Petersburg Formation) in Illinois. These lithotypes were analyzed petrographically and for meso- and micropore characteristics, functional group distribution using FTIR techniques, and fluidity. High-pressure CO2 adsorption isotherm analyses of these lithotypes were performed and, subsequently, all samples were reanalyzed in order to investigate the effects of CO2. After the high-pressure adsorption isotherm analysis was conducted and the samples were reanalyzed, there was a decrease in BET surface area for vitrain from 31.5m2/g in the original sample to 28.5m2/g, as determined by low-pressure nitrogen adsorption. Bright clarain and clarain recorded a minimal decrease in BET surface area, whereas for fusain there was an increase from 6.6m2/g to 7.9m2/g. Using low-pressure CO2 adsorption techniques, a small decrease in the quantity of the adsorbed CO2 is recorded for vitrain and bright clarain, no difference is observed for clarain, and there is an increase in the quantity of the adsorbed CO2 for fusain. Comparison of the FTIR spectra before and after CO2 injection for all lithotypes showed no differences with respect to functional group distribution, testifying against chemical nature of CO2 adsorption. Gieseler plastometry shows that: 1) softening temperature is higher for the post-CO2 sample (389.5??C vs. 386??C); 2) solidification temperature is lower for the post-CO2 sample (443.5??C vs. 451??C); and 3) the maximum fluidity is significantly lower for the post-CO2 sample (4 ddpm vs. 14 ddpm). ?? 2010 Elsevier B.V.

International Journal of Coal Geology↗

Depositional setting, petrology and chemistry of Permian coals from the Paraná Basin: 2. South Santa Catarina Coalfield, Brazil

In Brazil economically important coal deposits occur in the southern part of the Paraná Basin, where coal seams occur in the Permian Rio Bonito Formation, with major coal development in the states of Rio Grande de Sul and Santa Catarina. The current paper presents results on sequence stratigraphic interpretation of the coal-bearing strata , and petrological and geochemical coal seam characterization from the South Santa Catarina Coalfield, Paraná Basin. In terms of sequence stratigraphic interpretation the precursor mires of the Santa Catarina coal seams formed in an estuarine-barrier shoreface depositional environment , with major peat accumulation in a high stand systems tract (Pre-Bonito and Bonito seams), a lowstand systems tract (Ponta Alta seam, seam A, seam B) and a transgressive systems tract (Irapuá, Barro Branco and Treviso seams). Seam thicknesses range from 1.70 to 2.39 m, but high proportions of impure coal (coaly shale and shaley coal), carbonaceous shale and partings reduce the net coal thickness significantly. Coal lithoypes are variable, with banded coal predominant in the Barro Branco seam, and banded dull and dull coal predominantly in Bonito and Irapuá seams, respectively. Results from petrographic analyses indicate a vitrinite reflectance range from 0.76 to 1.63 %Rrandom (HVB A to LVB coal). Maceral group distribution varies significantly, with the Barro Branco seam having the highest vitrinite content (mean 67.5 vol%), whereas the Irapuá seam has the highest inertinite content (33.8 vol%). Liptinite mean values range from 7.8 vol% (Barro Branco seam) to 22.5 vol% (Irapuá seam). Results from proximate analyses indicate for the three seams high ash yields (50.2 – 64.2 wt.%). Considering the International Classification of in-Seam Coals, all samples are in fact classified as carbonaceous rocks (> 50 wt.% ash). Sulfur contents range from 3.4 to 7.7 wt.%, of which the major part occurs as pyritic sulfur. Results of X-ray diffraction indicate the predominance of quartz and kaolinite (also pyrite). Gypsum , gibbsite , jarosite and calcite were also identified in some samples. Feldspar was noted but is rare. The major element distribution in the three seams (coal basis) is dominated by SiO 2 (31.3 wt.%, mean value), Al 2 O 3 (14.5 wt.%, mean value) and Fe 2 O 3 (6.9 wt.%, mean value). Considering the concentrations of trace elements that are of potential environmental hazards the Barro Branco, Bonito and Irapuá seams (coal base) are significantly enriched in Co (15.7 ppm), Cr (54.5 ppm), Li (59.3 ppm), Mn (150.4 ppm), Pb (58.0 ppm) and V (99.6 ppm), when compared to average trace elements contents reported for U. S. coals. Hierarchical cluster analysis identified, based on similarity levels, three groups of major elements and seven groups of trace elements. Applying discriminant analyses using trace and major element distribution, it could be demonstrated that the three seams from Santa Catarina show distinct populations in the discriminant analyses plots, and also differ from the coals of Rio Grande do Sul analyzed in a previous study.

Santa Catarina↗

Measuring basin-scale aquifer storage change and mapping specific yield in Albuquerque, New Mexico, USA, with repeat microgravity data

Study Region The groundwater basin underlying the City of Albuquerque, New Mexico, USA. Study Focus The study focuses on changes in groundwater storage and how those changes relate to groundwater-level changes. Groundwater storage change was measured using repeat microgravity at 35 stations from 2016 to 2021. Usually, storage is monitored by converting groundwater-level changes to storage changes using the aquifer storage coefficient, a difficult property to measure. With gravity, storage change can be measured directly. The storage coefficient, or specific yield in an unconfined aquifer, was estimated using the gravity method at individual sites, and a map created showing how this property varies over the region. New Hydrological Insights for the Region For the first time, a map of specific yield was produced based on interpolated maps of gravity-derived storage change and groundwater-level change, allowing inference of this property over a broad region even without collocated monitoring wells and gravity stations. Gravity data indicate aquifer drawdown and recovery mainly occurs in the central part of the basin where pumping is greatest. This spatial distribution is not captured by the more widely spaced monitoring well network. Because the aquifer is recovering from historically greater-magnitude pumping, net-neutral storage change (inflow=outflow) occurs when pumping from the central part of the well field is about 1.54 × 10 7 cubic meters (12,500 acre-feet) per year.

New Mexico↗

Changes in streamflow seasonality associated with hydroclimatic variability in the north-central United States among three discrete temporal periods, 1946–2020

Study region North-central United States Study focus This study uses circular statistics to characterize the seasonal properties of annual maximum (AMS) and peaks-over-threshold (POT) streamflow time series for 841 and 623 selected U.S. Geological Survey (USGS) streamgages, respectively, without regulation or substantial diversion among common 75-, 50-, and 30-year trend periods through water year 2020 (the period from October 1, 2019, through September 30, 2020). A subset of AMS time series with detected change points (abrupt changes) in the median and (or) scale are analyzed on either side of the change point to evaluate changes in their circular statistics. New hydrologic insights for the region In the 50-year trend period, five regions share common mean flood timing in the AMS and POT partial duration series. Changes from asymmetric distributions to reflective symmetric distributions are detected particularly among the 50- and 30-year trend periods in the northernmost States of Minnesota, North Dakota, and Wisconsin. For the subset of streamgages with abrupt change points in the AMS, regional patterns of changes in seasonality are detected between the period of records before and after the change point. These findings can inform decisions related to the AMS used for flood frequency and potential mixed population analyses and flood control operations that may be affected by changes in when seasonal events occur, how long seasonal events last, and the long-term variability in the intensity and frequency of seasonal events.

Illinois, Iowa, Michigan, Minnesota, Missouri, Mon↗

Effects of climate on temporal variability in streamflow and salinity in the Upper Colorado River Basin

Study Region The Upper Colorado River Basin, a critical water source for more than 40 million people in the western United States. Study Focus Potential decreasing streamflow and elevated salinity concentrations threaten this resource. Climate variability has a large and well-studied effect on streamflow in the basin; however, the effect on salinity loading is less understood. This study investigates how snowpack dynamics, precipitation volume, and air temperature affect both streamflow and salinity at the basin scale from water years 1986–2021. New Hydrological Insights for the Region Climate variables explained 54 % of streamflow variability and 40 % of salinity variability across the basin. Both streamflow and salinity yields have declined in response to climate variability, but their response occurs on different timescales. Streamflow is more sensitive to snowpack, whereas salinity yields respond more strongly to antecedent precipitation. The delayed response of salinity yields may obscure the effects of both climate variability and salinity control measures. Residual analysis identified subbasins where the climate-salinity relation deviated from basin-wide patterns, suggesting that possible anthropogenic or other watershed processes may influence salinity loading in these areas. These novel findings underscore the importance of accounting for climate variability when evaluating long-term trends in streamflow and salinity.

Arizona, Colorado, New Mexico, Utah, Wyoming↗

Perceptions of volcanic air pollution and exposure reduction practices on the Island of Hawai‘i: Working towards socially relevant risk communication

Kīlauea volcano, on the Island of Hawai‘i, is one of the most active volcanoes in the world. Over the past four decades it has released large amounts of volcanic gases and aerosols which form volcanic air pollution known as ‘vog’. Communities downwind of Kīlauea have been chronically or episodically exposed to this potentially harmful air pollution and have raised concerns about the hazards of vog exposure. Public health and civil protection agencies have offered a range of advice, information, and mitigation strategies for living with vog. In this mixed-methods social study, we investigate the translation of official advice into practice in Island of Hawai‘i communities and assess how risk communication could be improved by considering public input, preferences, and community relevance. Given the paucity of information on the long-term effects of chronic vog exposure, assessing the effectiveness of public health and risk communication is vital.

Hawaii↗

Application of deterministic deconvolution of ground-penetrating radar data in a study of carbonate strata

We successfully applied deterministic deconvolution to real ground-penetrating radar (GPR) data by using the source wavelet that was generated in and transmitted through air as the operator. The GPR data were collected with 400-MHz antennas on a bench adjacent to a cleanly exposed quarry face. The quarry site is characterized by horizontally bedded carbonate strata with shale partings. In order to provide groundtruth for this deconvolution approach, 23 conductive rods were drilled into the quarry face at key locations. The steel rods provided critical information for: (1) correlation between reflections on GPR data and geologic features exposed in the quarry face, (2) GPR resolution limits, (3) accuracy of velocities calculated from common midpoint data and (4) identifying any multiples. Comparing the results of deconvolved data with non-deconvolved data demonstrates the effectiveness of deterministic deconvolution in low dielectric-loss media for increased accuracy of velocity models (improved at least 10-15% in our study after deterministic deconvolution), increased vertical and horizontal resolution of specific geologic features and more accurate representation of geologic features as confirmed from detailed study of the adjacent quarry wall. ?? 2004 Elsevier B.V. All rights reserved.

Journal of Applied Geophysics↗

Feasibility of waveform inversion of Rayleigh waves for shallow shear-wave velocity using a genetic algorithm

Conventional surface wave inversion for shallow shear (S)-wave velocity relies on the generation of dispersion curves of Rayleigh waves. This constrains the method to only laterally homogeneous (or very smooth laterally heterogeneous) earth models. Waveform inversion directly fits waveforms on seismograms, hence, does not have such a limitation. Waveforms of Rayleigh waves are highly related to S-wave velocities. By inverting the waveforms of Rayleigh waves on a near-surface seismogram, shallow S-wave velocities can be estimated for earth models with strong lateral heterogeneity. We employ genetic algorithm (GA) to perform waveform inversion of Rayleigh waves for S-wave velocities. The forward problem is solved by finite-difference modeling in the time domain. The model space is updated by generating offspring models using GA. Final solutions can be found through an iterative waveform-fitting scheme. Inversions based on synthetic records show that the S-wave velocities can be recovered successfully with errors no more than 10% for several typical near-surface earth models. For layered earth models, the proposed method can generate one-dimensional S-wave velocity profiles without the knowledge of initial models. For earth models containing lateral heterogeneity in which case conventional dispersion-curve-based inversion methods are challenging, it is feasible to produce high-resolution S-wave velocity sections by GA waveform inversion with appropriate priori information. The synthetic tests indicate that the GA waveform inversion of Rayleigh waves has the great potential for shallow S-wave velocity imaging with the existence of strong lateral heterogeneity.

Journal of Applied Geophysics↗