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William C. Evans

Publications and source records attributed to William C. Evans.

At least 73 records · Page 4Linked to original sources
USGS2003

Excess nitrogen in selected thermal and mineral springs of the Cascade Range in northern California, Oregon, and Washington: Sedimentary or volcanic in origin?

Anomalous N 2 /Ar values occur in many thermal springs and mineral springs, some volcanic fumaroles, and at least one acid-sulfate spring of the Cascade Range. Our data show that N 2 /Ar values are as high as 300 in gas from some of the hot springs, as high as 1650 in gas from some of the mineral springs, and as high as 2400 in gas from the acid-sulfate spring on Mt. Shasta. In contrast, gas discharging from hot springs that contain nitrogen and argon solely of atmospheric origin typically exhibits N 2 /Ar values of 40–80, depending on the spring temperature. If the excess nitrogen in the thermal and mineral springs is of sedimentary origin then the geothermal potential of the area must be small, but if the nitrogen is of volcanic origin then the geothermal potential must be very large. End-member excess nitrogen (δ 15 N) is +5.3‰ for the thermal waters of the Oregon Cascades but is only about +1‰ for fumaroles on Mt. Hood and the acid-sulfate spring on Mt. Shasta. Dissolved nitrogen concentrations are highest for thermal springs associated with aquifers between 120 and 140°C. Chloride is the major anion in most of the nitrogen-rich springs of the Cascade Range, and N 2 /Ar values generally increase as chloride concentrations increase. Chloride and excess nitrogen in the thermal waters of the Oregon Cascades probably originate in an early Tertiary marine formation that has been buried by the late Tertiary and Quaternary lava flows of the High Cascades. The widespread distribution of excess nitrogen that has been generated in low to moderate-temperature sedimentary environments is further proof of the restricted geothermal potential of the Cascade Range.

Cascade Range↗
USGS2003

Scrubbing masks magmatic degassing during repose at Cascade-Range and Aleutian-Arc volcanoes

Between 1992 and 1998, we sampled gas discharges from ≤173°C fumaroles and springs at 12 quiescent but potentially restless volcanoes in the Cascade Range and Aleutian Arc (CRAA) including Mount Shasta, Mount Hood, Mount St. Helens, Mount Rainier, Mount Baker, Augustine Volcano, Mount Griggs, Trident, Mount Mageik, Aniakchak Crater, Akutan, and Makushin. For each site, we collected and analyzed samples to characterize the chemical (H2O, CO2, H2S, N2, CH4, H2, HCl, HF, NH3, Ar, O2, He) and isotopic (δ13C of CO2, 3He/4He, 40Ar/36Ar, δ34S, δ13C of CH4, δ15N, and δD and δ18O of water) compositions of the gas discharges, and to create baseline data for comparison during future unrest. The chemical and isotopic data show that these gases contain a magmatic component that is heavily modified from scrubbing by deep hydrothermal (150° - 350°C) water (primary scrubbing) and shallow meteoric water (secondary scrubbing). The impact of scrubbing is most pronounced in gas discharges from bubbling springs; gases from boiling-point fumaroles and superheated vents show progressively less impact from scrubbing. The most effective strategies for detecting gas precursors to future CRAA eruptions are to measure periodically the emission rates of CO2 and SO2, which have low and high respective solubilities in water, and to monitor continuously CO2 concentrations in soils around volcanic vents. Timely resampling of fumaroles can augment the geochemical surveillance program by watching for chemical changes associated with drying of fumarolic pathways (all CRAA sites), increases in gas geothermometry temperatures (Mount Mageik, Trident, Mount Baker, Mount Shasta), changes in δ13C of CO2 affiliated with magma movement (all CRAA site), and increases in 3He/4He coupled with intrusion of new magma (Mount Rainier, Augustine Volcano, Makushin, Mount Shasta). Repose magmatic degassing may discharge substantial amounts of S and Cl into the edifices of Mount Baker and several other CRAA volcanoes that is trapped by primary and secondary scrubbing. The consequent acidic fluids produce ongoing alteration in the 0.2- to 3-km-deep hydrothermal systems and in fields of boiling-point fumaroles near the surface. Such alteration may influence edifice stability and contribute to the formation of more-hazardous cohesive debris flows. In particular, we recommend further investigation of the volume, extent, and hazards of hydrothermal alteration at Mount Baker. Other potential hazards associated with the CRAA volcano hydrothermal systems include hydrothermal eruptions and, for deeper systems intruded by magma, deep-seated edifice collapse.

Alaska;British Columbia;California;Oregon;Washingt↗
USGS2003

Mantle and Crustal Sources of Carbon, Nitrogen, and Noble gases in Cascade-Range and Aleutian-Arc Volcanic gases

Here we report anhydrous chemical (CO2, H2S, N2, H2, CH4, O2, Ar, He, Ne) and isotopic (3He/4He, 40Ar/36Ar, δ13C of CO2, δ13C of CH4, δ15N) compositions of virtually airfree gas samples collected between 1994 and 1998 from 12 quiescent but potentially restless volcanoes in the Cascade Range and Aleutian Arc (CRAA). Sample sites include ≤173°C fumaroles and springs at Mount Shasta, Mount Hood, Mount St. Helens, Mount Rainier, Mount Baker, Augustine Volcano, Mount Griggs, Trident, Mount Mageik, Aniakchak Crater, Akutan, and Makushin. The chemical and isotopic data generally point to magmatic (CO2, Ar, He), shallow crustal sedimentary (hereafter, SCS) (CO2, N2, CH4), crustal (He), and meteoric (N2, Ar) sources of volatiles. CH4 clearly comes from SCS rocks in the subvolcanic systems because CH4 cannot survive the higher temperatures of deeper potential sources. Further evidence for a SCS source for CH4 as well as for non-mantle CO2 and non-meteoric N2 comes from isotopic data that show wide variations between volcanoes that are spatially very close and similar isotopic signatures from volcanoes from very disparate areas. Our results are in direct opposition to many recent studies on other volcanic arcs (Kita and others, 1993; Sano and Marty, 1995; Fischer and others, 1998), in that they point to a dearth of subducted components of CO2 and N2 in the CRAA discharges. Either the CRAA volcanoes are fundamentally different from volcanoes in other arcs or we need to reevaluate the significance of subducted C and N recycling in convergent-plate volcanoes.

Alaska;British Columbia;California;Oregon;Washingt↗
USGS2003

Shallow soil CO2 flow along the San Andreas and Calaveras Faults, California

We evaluate a comprehensive soil CO2 survey along the San Andreas fault (SAF) in Parkfield, and the Calaveras fault (CF) in Hollister, California, in the context of spatial and temporal variability, origin, and transport of CO2 in fractured terrain. CO2 efflux was measured within grids with portable instrumentation and continously with meteorological parameters at a fixed station, in both faulted and unfaulted areas. Spatial and temporal variability of surface CO2 effluxes was observed to be higher at faulted SAF and CF sites, relative to comparable background areas. However, ??13C (-23.3 to - 16.4???) and ??14C (75.5 to 94.4???) values of soil CO2 in both faulted and unfaulted areas are indicative of biogenic CO2, even though CO2 effluxes in faulted areas reached values as high as 428 g m-2 d-1. Profiles of soil CO2 concentration as a function of depth were measured at multiple sites within SAF and CF grids and repeatedly at two locations at the SAF grid. Many of these profiles suggest a surprisingly high component of advective CO2 flow. Spectral and correlation analysis of SAF CO2 efflux and meteorological parameter time series indicates that effects of wind speed variations on atmospheric air flow though fractures modulate surface efflux of biogenic CO2. The resulting areal patterns in CO2 effluxes could be erroneously attributed to a deep gas source in the absence of isotopic data, a problem that must be addressed in fault zone soil gas studies.

Journal of Geophysical Research B: Solid Earth↗
USGS2002

Tracing and quantifying magmatic carbon discharge in cold groundwaters: Lessons learned from Mammoth Mountain, USA

A major campaign to quantify the magmatic carbon discharge in cold groundwaters around Mammoth Mountain volcano in eastern California was carried out from 1996 to 1999. The total water flow from all sampled cold springs was ??? 1.8 ?? 107 m3/yr draining an area that receives an estimated 2.5 ?? 107 m3/yr of recharge, suggesting that sample coverage of the groundwater system was essentially complete. Some of the waters contain magmatic helium with 3He/4He ratios as high as 4.5 times the atmospheric ratio, and a magmatic component in the dissolved inorganic carbon (DIC) can be identified in virtually every feature sampled. Many waters have a 14C of 0-5 pmC, a ??13C near -5???, and contain high concentrations (20-50 mmol/1) of CO2(aq); but are otherwise dilute (specific conductance = 100-300 ??S/cm) with low pH values between 5 and 6. Such waters have previously escaped notice at Mammoth Mountain, and possibly at many other volcanoes, because CO2 is rapidly lost to the air as the water flows away from the springs, leaving neutral pH waters containing only 1-3 mmol/1 HCO-3. The total discharge of magmatic carbon in the cold groundwater system at Mammoth Mountain is ~ 20 000 t/yr (as CO2), ranging seasonally from about 30 to 90 t/day. Several types of evidence show that this high discharge of magmatic DIC arose in part because of shallow dike intrusion in 1989, but also demonstrate that a long-term discharge possibly half this magnitude (~ 10 000 t/yr) predated that intrusion. To sustain a 10 000 t/yr DIC discharge would require a magma intrusion rate of 0.057 km3 per century, assuming complete degassing of magma with 0.65 wt% CO2 and a density of 2.7 t/m3. The geochemical data also identify a small ( < 1 t/day) discharge of magmatic DIC that can be traced to the Inyo Domes area north of Mammoth Mountain and outside the associated Long Valley caldera. This research, along with recent studies at Lassen Peak and other western USA volcanoes, suggests that the amount of magmatic carbon in cold groundwaters is important to constraining rates of intrusion and edifice weathering at individual volcanoes and may even represent a significant fraction of the global carbon discharge from volcanoes. ?? 2002 Elsevier Science B.V. All rights reserved.

Journal of Volcanology and Geothermal Research↗
USGS2002

Report of hydrologic investigations in the Three Sisters area of central Oregon, Summer 2001

An ongoing episode of crustal uplift centered in the Separation Creek drainage of the Three Sisters area, central Oregon Cascades, may result from a magmatic intrusion that began in 1998. An investigation of springs in this drainage in summer 2001 revealed slightly elevated water temperatures and chloride (Cl-) concentrations of up to about 5?C and 20 milligrams per liter (mg/L), respectively, above background. The total discharge of anomalous Cl- in Separation Creek was 9.2 grams per second, which in combination with the temperature-Cl- relation in the springs results in a total advective heat discharge of 16 MW (megawatts). Comparison with similar findings obtained a decade earlier suggests that total Cl- and heat discharges in the groundwater drainage are unaffected by the current uplift. However, the isotopic composition of the dissolved inorganic carbon (DIC) in the spring waters (delta carbon-13 (13C) = -9.03 to -11.6?; carbon-14 (14C) <25 pmC) combined with helium-3/helium-4 (3He/4He) ratios near 8 RA and C/3He ratios <1010 in two of the springs are indicative of a magmatic source. The high 3He/4He ratios indicate that the magmatic gas is derived from a relatively recent, if not ongoing, intrusion. The concentration of magmatic carbon is low, a few millimoles per liter (mmol/L) at most, with an average value of 1.53 mmol/L for all the springs sampled in the drainage. Combining this average with the late-summer water flow in Separation Creek suggests a discharge of 21 tonnes/day of magmatic carbon dioxide (CO2). The presence of magmatic carbon in the shallow groundwater system, and the fact that DIC is uncorrelated with Cl-, suggests that some magmatic gas could escape diffusely through the soils.

Water-Resources Investigations Report↗
USGS2002

Mantle helium and carbon isotopes in Separation Creek geothermal springs, Three Sisters area, central Oregon: Evidence for renewed volcanic activity or a long term steady state system?

Here we present the helium and carbon isotope results from the initial study of a fluid chemistry-monitoring program started in the summer of 2001 near the South Sister volcano in central Oregon. The Separation Creek area which is several miles due west of the volcano is the locus of strong crustal uplift currently occurring at a rate of 4-5 cm/yr (Wicks, et. al. , 2001). Helium [R C /R A = 7.44 and 8.61 R A (R C /R A = ( 3 He/ 4 He) sample-air corrected /( 3 He/ 4 He) air ))] and carbon (δ 13 C = -11.59 to -9.03 ‰ vs PDB) isotope data and CO 2 / 3 He (5 and 9 x 10 9 ) show that bubbling cold springs in the Separation Creek area near South Sister volcano carry a strong mantle signal, indicating the presence of fresh basaltic magma in the volcanic plumbing system. There is no evidence though, to directly relate this signal to the crustal uplift that is currently taking place in the area, which started in 1998. The geothermal system in the area is apparently much longer lived and shows no significant changes in chemistry compared to data from the early 1990s. Hot springs in the area, which are relatively far removed from the volcanic edifice, do not carry a strong mantle signal in helium isotope ratios (2.79 to 5.08 R A ), unlike the cold springs, and also do not show any significant changes in helium isotope ratios compared to literature data for the same springs of over two decades ago. The cold springs of the Separation Creek area form a very diffuse but significant low temperature geothermal system, that should, due to its close vicinity to the center of up uplift, be more sensitive to changes in the deeper volcanic plumbing system than the far removed hot springs and therefore require much more study and consideration when dealing with volcano monitoring in the Cascade range or possibly with geothermal exploration in general.

Oregon↗
USGS2000

Invisible CO2 gas killing trees at Mammoth Mountain, California

Since 1980, scientists have monitored geologic unrest in Long Valley Caldera and at adjacent Mammoth Mountain, California. After a persistent swarm of earthquakes beneath Mammoth Mountain in 1989, geologists discovered that large volumes of carbon dioxide (CO2 ) gas were seeping from beneath this volcano. This gas is killing trees on the mountain and also can be a danger to people. The U.S. Geological Survey (USGS) continues to study the CO2 emissions to help protect the public from this invisible potential hazard.

Fact Sheet↗
USGS2000

Hydrothermal activity and carbon-dioxide discharge at Shrub and upper Klawasi mud volcanoes, Wrangell Mountains, Alaska

Shrub mud volcano, one of three mud volcanoes of the Klawasi group in the Copper River Basin, Alaska, has been discharging warm mud and water and CO2?rich gas since 1996. A field visit to Shrub in June 1999 found the general level of hot-spring discharge to be similar, but somewhat more widespread, than in the previous two years. Evidence of recent animal and vegetation deaths from CO2 exposure were confined to localized areas around various gas and fluid vents. Maximum fluid temperatures in each of three main discharge areas, ranging from 48-54?C, were equal to or higher than those measured in the two previous years; such temperatures are significantly higher than those observed intermittently over the past 30 years. At Upper Klawasi mud volcano, measured temperatures of 23-26?C and estimated rates of gas and water discharge in the summit crater lake were also similar to those observed in the previous two years. Gas discharging at Shrub and Upper Klawasi is composed of over 98% CO2 and minor amounts of meteoric gases (N2, O2, Ar) and gases partly of deeper origin (CH4 and He). The rate of CO2 discharge from spring vents and pools at Shrub is estimated to be ~10 metric tonnes per day. This discharge, together with measured concentrations of bicarbonate, suggest that a total CO2 upflow from depth of 20-40 metric tonnes per day at Shrub.Measurements were made of diffuse degassing rates from soil at one ~300 m2 area near the summit of Shrub that included vegetation kill suggestive of high CO2 concentrations in the root zone. Most of measured gas flow rates in this area were significantly higher than background values, and a CO2 concentration of 26 percent was measured at a depth of 10 cm where the gas flow rate was highest. Although additional measurements of diffuse gas flow were made elsewhere at Shrub, no other areas of vegetation kill related to diffuse degassing and high soil-gas CO2 concentrations could be seen from the air.Chemical and isotopic compositions of the gas and water discharging at Shrub and Upper Klawasi indicate derivation from a combination of mantle (magmatic) and crustal (marine sedimentary rock) sources and suggest a common fluid reservoir at depth. In particular, both the total dissolved carbon and values of 13C in CO2 are similar for fluids and gas sampled at each area, and do not appear to have changed with the onset of increased spring temperatures and fluid discharge at Shrub. This suggests that the underlying cause of the recent changes in discharge rate and temperature at Shrub is not an increase in the rate of input of magmatic heat and volatiles, but rather increases in the permeability of the upflow conduits that connect the gas-rich reservoir to the surface.

Water-Resources Investigations Report↗
USGS1997

Multiple source components in gas manifestations from north-central Italy

Gas manifestations in north-central Italy consist of CO2-rich gases with minor N2-rich emissions and discharge either along with thermal springs or into cold and stagnant waters. 'Cold' gases are prevalently CO2-dominated (> 90%) while gases related to the thermal waters have variable composition: from CO2 > 99.5% to N2 > 90%. The variable composition of 'thermal' gases is caused by differences in the thermal regime and lithology of the ascent paths, where there is mixing of gases from multiple sources, such as N2-rich atmospheric and deep CO2-rich metamorphic end-members. Elevated concentrations of CH4 and H2 in these gases are generally related to the presence of active geothermal systems at shallow depth, such as the Larderello-Travale field in Tuscany. The ??13C values between coexisting CH4 and CO2 in all samples analyzed suggest that CH4 originates abiogenically in 200-400??C hydrothermal systems. Far from geothermal areas, where the thermal gradient is lower or the water/gas ratio is high because of large inflow of meteoric waters, H2 and CH4 are usually lower. In some cases, they can be scrubbed or oxidized (especially H2), while the residual rising gas becomes indirectly enriched in N2 and CO2. Carbon dioxide is also enriched in some discharged gases because it is produced at shallow depth in lower temperature conditions (< 150??C). Heavy ??15N values for N2 to near +7.0??? suggest that, for some gas samples that contain excess nitrogen (e.g. where N2/Ar ??? 83), this component probably derives from ammonia-rich feldspars and micas within the Palaeozoic schist basement rocks. However, other samples show evidence of a shallow component of CH4 and N2 from Neogene basin sediments. The areal distribution of the 3He/4He ratio points to a general prevalence of atmospheric and crustal 4He in the gas discharges in central Italy. A significant component of mantle 3He is only found in the geothermal areas of Larderello where the large regional thermal anomaly suggests the presence of a deep magmatic body. ?? 1997 Elsevier Science B.V.

Chemical Geology↗
USGS1997

Mantle fluids in the San Andreas fault system, California

Fluids associated with the San Andreas and companion faults n central and south-central California have high 3He/4He ratios. The lack of correlation between helium isotopes and fluid chemistry or local geology requires that fluids enter the fault system from the mantle. Mantle fluids passing through the ductile lower crust must enter the brittle fault zone at or near lithostatic pressures; estimates of fluid flux based on helium isotopes suggest that they may thus contribute directly to fault-weakening high-fluid pressures at seismogenic depths.

Science↗
USGS1997

Geochemistry of natural gas manifestions from the Upper Tiber Valley (central Italy)

Six natural gas manifestions from the upper Tiber Valley at Caprese Michelangela and Pieve S. Stefano (Arezzo) and at Umbertide (Pertugia) localities have been analysed for major, minor, trace gas compositions, as well as for ??13C in CO2 and CH4, ??15N in N2 and 3He/4He isotopic ratios. All gas emissions are CO2-rich (???94%), with N2 contents of 4-5%. Those from Caprese and Pieve S. Stefano have very peculiar compsitions when compared to other gases from northern-central Apennines. Apart from CO2, these gases show relatively high contents of He (with crustal isotopic ratios) and medium to high temperature-related gases such as CO, H2 and C6H6. Although located quite far from the geothermal areas in Tuscany, the application of several gas geothermetric techniques suggest for these gases deep equilibrium tempratures of about 300??C. Moreover, the ??13C in CO2 and CH4 (~.4.0% and -38.0%, respectively) and the ??13N values in N2 (+0.064 to +0.84%) would seem to imply a multiple deep source for these gases.

Mineralogica et Petrographica Acta↗
USGS1996

Chemical and isotopic characteristics of fluids along the cameroon volcanic line, cameroon

Results of the chemical and isotopic analysis of the water and gases discharged from volcanic crater lakes and soda springs located along the Cameroon Volcanic Line were used to characterize and infer their genetic relationships. Variations in the solute compositions of the waters indicate the dominant influence of silicate hydrolysis. Na+ (40-95%) constitutes the major cation in the springs while Fe2+ + Mg2+ (70%) dominate in the CO2-rich lakes. The principal anion is HCO3 (>90%), except in the coastal springs where Cl predominates. Lakes Nyos and Monoun have Fe-Mg-Ca-HCO3 type signatures; the soda springs are essentially Na-HCO3 type, while all other lakes show similar ionic compositions to dilute surface waters. Dissolved gases show essentially CO2 (>90%), with small amounts of Ar and N2, while CH4 constitutes the principal component in the non-gassy lakes. Active volcanic gases are generally absent, except in the Lobe spring with detectable H2S. Stable isotope ratio evidence indicates that the bicarbonate waters are essentially of meteoric origin. CO2 (??13C = -2 to -8???) and He (3He/4He = 1 to 5.6Ra) infer a mantle contribution to the total CO2. CH4 has a biogenic source, while Ar and N2 are essentially atmospheric in origin, but mixing is quite common.

Journal of African Earth Sciences↗