Economic Geology Vol. 60, 1965, pp. 1411-1421 HYDROTHERMAL ALTERATION IN GS-3 AND GS-4 DRILL HOLES, MAIN TERRACE, STEAMBOAT SPRINGS, NEVADA • ROBERT SCHOEN AND DONALD E. WHITE ABSTRACT Hot spring waters at SteamboatSprings;Nevada,depositsmall amountsof mercury,antimony,gold,and silverand hydrothermally alter the rocksthroughwhichthey flow. Two patternsof alterationcan be recognized in the granodiorite bedrockunderlyingthe Main Terrace:an ill-defined patternof alterationrelatedto depth,anda moredistinctpattern consisting of zonesof variousmineralassemblages envelopingfractures. The alterationmineral assemblages relatedto fracturesresemble the alterationmineral assemblages in granodioriteof the Butte, Montana, coppermining district. Alteration relatedto depth includesthe replacementof someplagioclaseby hydrothermalK-feldsparin the upper300 feet of the springsystem, and the formation of albite and calcite from calcic plagioclaseat depthsgreaterthan about200 feet. Near fractures,hornblendeis the mostreactivemineral and is replaced by randommixed-layerillite-montmorillonite and iron-richchlorite. Bio- tite alters pseudomorphically to chlorite. Calcic plagioclasealters to mixed-layer illite-montmorillonite.Plutonic K-feldspar and quartz are generally unaffected. The mostintensealterationis immediatelyadjacentto fractureswhere all feldspars andpreviously formedchlorite,mixed-layerillite-montmorillonite, and calciteare replacedby illitc (with lessthan 10 percentinterlayeredmontmorillonite),quartz,andpyrite. The K+/H + ratio in the deep high-temperaturewaters suggeststhat the waters are in equilibrium with K-mica as determinedby Hemley's reaction studies. Therefore, the present-dayspring waters may still be producingthe observed hydrothermalalteration. This hypothesis, coupled with the proven ability of thesewaters to depositmetals, indicatethat the springwatersare similar to someore-formingfluids. STEAMBOAT SPRINGS, NEVADA,is an area of hot springactivityin southern WashoeCountynear the California-Nevada boundary(Fig. 1). Because mercury,antimony,gold, and silver are being depositedby the hot waters, the springshavelong beenof interestto economic geologists (7, 2, 15, p. 110-113). The possibilitythat the thermalwaterswill be usefulin characterizing ancientore-formingsolutionsis enhancedby the nearnessof the springsystemto the celebratedgold-silverdepositsof the ComstockLode and to epithermalmercurydeposits(13). A summaryof pastgeologicstudiesin the area was givenby Branno& and others(2), and White and others(16). The alterationmineralogyin Publication authorized by the Director, U.S. GeologicalSurvey. 1411 1412 R.SCHOEN ANDD.E.WHITE N ,• EXPLANATION NEVADA st#me,oat sm•n•s I----'--"1 • Z GS-3 ': FIG.1. Generalized geologic map'of Steamboat Springs thermal area,Washoe County, Nevada.(Fromdetailed map, D.'E.Whiteandothers, 1964.) corefromfourdrillholes at Steamboat Springs wasdescribed bySigvaldason andWhite(11,12). Thepresent report describes thealteration mineralogy in the'corefromtwomoredrillholes in theMainTerrace, themostactive partof thearea,andconsiders brieflytherelationships between thealteration and the presentspringwaters. HYDROTHERMAL ALTERATION IN DRILL HOLES 1413 The patternof rock alterationobservedat SteamboatSpringsis similar to that reportedfrom Butte, Montana, and other famousmining districts, and we considerit probablethat the present-daywaters are still producing this alteration. Therefore, in spite of the fact that the metal depositsat SteamboatSpringsare not rich enoughto be classedas ore (2), the presentday thermal waters may be similar to someore-formingsolutions. The basementrocks of the thermal area consistof a granodioritepluton of late Mesozoicage intrudedinto metasediments and metavolcanics of probable early Mesozoicage. Tertiary and Quaternaryvolcanicrockswere extruded on the eroded surface of this basement, and andesite dikes were intruded into the granodiorite. Alluvium and silicioussinter were deposited intermittentlyduring and after the last volcaniceruptions. The generalized geologyand the locationsof drill holes, springs,and fissure systemsare presentedin Figure 1. The drill holesdescribedin this report, GS-3 and GS-4, intersectonly granodioritebedrock,below the surficial alluvium and sinter. METHODS The mineralogyof the rockswas determinedby X-ray diffraction,microscopicstudy of thin sections,and chemicaland spectrographicanalyses. X-ray mineralogicanalysiswas performedon 5 gram samplesground dry for 15 minutesand packedin standard2 cm aluminummounts. Clay minerals were concentrated by centrifugingan aqueoussuspension and making two successive withdrawalswith a pipette of a small amount of suspension containingthe lessthan 2 • size material (3). The <2 • >0.5 • fraction was then sedimentedon a glassslide for X-ray diffraction analysis Significantmineralogicvariationsin the drill core were determinedprimarily by X-ray methods. X-ray diffractogramsof three samplesof fresh granodioritefrom outsidethe hot spring area were the basis for a semiquantitativeevaluationof changesin mineralogyeffectedby alteration. A strongX-ray peak, mostnearly free from interference,was studiedfor eachmineral. The maximumpeak heightfor a mineral, on diffractograms of the three fresh granodiorites,was equatedwith the averagevolume percentageof the mineral reported by modal analyses. The maximum peak heightwas usedso that any reductioncouldbe related directlywith degree of alteration. A further checkon the peak heightof quartz was obtainedby calibratingagainstknown artificial and natural rock standards. The amount of quartz determinedagainstknown standardswas 2 to 4 percent less than that reportedby modal analyses. Comparisonof the maximum X-ray peak height in the fresh granodiorite with the peak height in altered granodioritegave a proportion that was assumedto be linearly relatedto the percentageof the mineral presentin the alteredrock. We are aware that this assumptionis not strictly valid and for this reason calculated abundances are considered to be no more than semi- quantitative. The volumepercentage increaseof all the alterationphaseswas considered to dqualthe volumepercentage decrease of all the primary phases 1414 R. SCHOBN .4ND D. B. I/FHITB andthe distribution of alteration phases wasagainconsidered to be linearly related to peak heights. AlthoughmodalandX-ray analyses of the threesamples of freshgranodioriteindicatedthat quartzwas a relativelyconstant25 percent,X-ray resultsfor quartzfrom piecesof almostfresh drill core rangedfrom 20 to 30 vercentbasedon the knownstandards. Two samplesGS-3-513 and GS-3- 685 gavevaluesof 16 and 18 percentquartz,respectively.As thin sections showthat quartzis not replacedduringhydrothermal alteration,this slight variationin quartz valuesis probablyrelatedto the difficultyof selecting representativerock chips from small piecesof diamonddrill core. For this reason,X-ray peaksof quartz from alteredrockswere interpretedas signifying25 percentof the rockif theyfell withinthe limitsof 16 to 30 percent notedfor the fairly freshgranodiorite. Only whenthe quartzpeaksexceeded theselimits was a greaterpercentageof the rock consideredto be quartz. This samereasoningcannotbe appliedto the other primary mineralsin the. rocks becausethese mineralsare all replacedto some degree by the alteration. The accuracyof this method is undoubtedlylow; however, its ability to pick up major and even minor changesin mineralogyhas been verified in this study. MINERALOGY Fresh granodioritefrom just outsidethe springarea containsplagiodase feldspar(oscillatoryzoningnear andesinewith rims of oligoclase),quartz. orthoclase,biotite, hornblende,and chlorite in decreasingorder of abundance. The minor chloriteindicatesthat eventhis granodioriteis not entirelyfresh. Granodiorite within the spring area is altered in relation to its distance from flow channelsand presumablyto the size and length of time eachflow channelhas existed. In addition,there is an ill-definedpattern of alteration relatedto depth. However, eventhe freshestgranodioritefrom the diamond drill holes is devoid of hornblendeexcept sporadicallynear the surface in GS-1 drill hole (11, p. Dl17). Hornblendeis clearly the most unstable mineral in the hydrothermalenvironment. Drill Hole GS-$.--The fissuresystemof the Main Terrace, along which alterationis mostintense,dips to the east,away from GS-3 (Fig. 1; detailed log in White andothers,1964,table3). Hence,the granodiorite is relatively fresh except near fractures. Abundancesof mineralscomputedfrom the X-ray data are plottedsemiquantitatively in Figure 2. Major variationsin percentages of the mineralsoccurat shearzonesand veins,whichare indicatedalongthe right sideof Figure 2. Samplingwasnot sufficiently closely spaced to defineall zonesof intensealteration. Alteration controlledby fracturescan be divided arbitrarily into a less intensezone of argillization away from fractures and an intenselyaltered zone of sericitizationadjacent to fractures. The intensity of alteration is consideredhere to be the degree to which hydrogen metasomatismhas affectedthe rock (6). Thin sectionsshow that in the argillic zone biotite is first bleachedand HYDROTHERMAL ALTERATION IN DRILL HOLES 1415 then is replacedby chlorite. The chlorite replacesthe bleachedbiotite pseudomorphically withoutany visiblechangein volme and with the same crystallographic orientation.The morecalciccoresof the zonedplagioclase APPROXIMATE PERCENTAGES APPROXIMATE P[RCENTAGES 0 O• PRINCIPAL MINERALS 25 50 I I o•,.'•.•.• •, 2.2 •0 Mm 75 I M(•i• •k MM• cmq4•niq II•, K-f,d•, W/ OF PRINCIPAL MINERALS I9O 0 Lw•e* /• • / 16 25 50 75 I I I 19O W•ler ' tible Opaline sinter with•-cdstoMlite increasing w•th depth Alluvium containing quartz, K-feldspar, plagk)- ciasa andillite,pyrite, kaolinite, andl•-cristohalite 139 105 172 141 149 193 ) ? o,,-- -v,,. I/ ,,½ fit • .• • .-. x '• •, 232 257 ', \ '\ • /// ,, Z•// 295 I /t•/ / L•/ //'7 , % ', /•'/ ??? . '•,X I// ...' /' 261 378 355 4• 2 423 - I I I•1 / let o'• 320 I I / ,, o, g.9 / / //! _= tl E ,• =e •/.• ,'/./ I G I • •: To- , G I I I • = • • % -- - •, I 475 356 ,,, ,,, ,,,',,4O4 412 \ \ • •b ,• • \ xx• x. • Xo • 432 / 459 / / / / I • 476 '& t / q 9 d /ß / i/ •/ •o II t t m •x• •o •• '• ,, tl • x• • zone e TIL •r zone r • • og • // / / o •V•nlet 49O 505 GS-3 GS-4 Fro. 2 (Left) Semiquantitative plot of mineralogyfrom drill hole GS-3, Main Terrace, SteamboatSprings. Straight lines arbitrarily drawn betweenpointsof observation. Ch = chlorite. Fro. 3. (Right) Semiquantitative plot of mineralogyfrom drill hole GS-4, Main Terrace,Steamboat Springs. Straightlinesarbitrarilydrawnbetweenpoints of observation. 1416 R. SCHOEN AND D. E. WHITE crystalsare replaced by fine-grained wormymixed-layerillite-montmorillonite with low birefringenceand a low index of refractionof about 1.53 or less. Quartz and orthoclase are unalteredin the argilliczone. In the sericiticzoneadjacentto fractures, onlyillite (sericiteof Hemley and Jones,1964, p. 542) quartz, and pyrite appearto be stable. Finegrainedillite with lessthan 10 percentinterlayeredmontmorilloniteand with fairly high birefringence is produced from the mixed-layerillite-montmorilloniteof the argilliczone. Illite alsoreplacesall remainingplagioclase and some orthoclase;where carried to completionall orthoclaseis replaced. Chlorite,an alterationproductitself,is replaced pseudomorphically by coarsegrainedwhite micathat is probablychemically similarto the illite, and by pyrite. Chalcedonic silicaformsin the sericiticzone,presumably from silica that is releasedby alterationof silicatesin boththe argillicand sericiticzones. The intensealterationof the sericiticzone overridesall lesserdegreesof alterationincludingthat relatedto depth. Most of the fracturesenclosedby sericitizedgranodioriteare filled with calcite,chalcedony, and quartz. Abovethe depthof 174 feet calciteis absent from theseveins,evidentlybecauseof the increasingsolubilityof calcitewith decreasing temperature. Away from fractures,in the argillic zonethat constitutes mostof the rock in GS-3 drill hole,certainmineralogic changes relatedto depthcanbe defined. At depthsgreaterthan about200 feet the calciccoresof plagioclase crystals are sometimes replacedby albitethat is crystallographically parallelor nearly parallelto the originalsodicrims. Patchesof calcitealsoare foundreplacing the coresof calcicplagioclase crystalsat depthsgreater than about200 feet. Thesemineralsoccurin additionto, ratherthaninsteadof, mixed-layerillitemontmorillonite. Abovea depthof about300 feet someplagiodaseis replacedby hydrothermal K-feldsparin a mannersimilar to, but muchlessextensivethan, that describedby Sigvaldasonand White (12) in the upper part 9f GS-5 drill hole. The hydrothermalK-feldspar is not distinguishedfrom original orthodasein Figure 2. As previouslystated,the intensealterationof the sericiticzonedestroys the alterationmineralsof the argillic zoneas well as the alterationminerals relatedto depth. However, the degreeof developmentof the sericiticzone is itself related to depth, being somewhatweaker near the surface. For this reason,completereplacementis not alwayseffectedin shallowsericiticzones. X-ray diffractograms of the <2 t• fractionshowthat the hydrothermal clay rangesfrom a well crystallized illite (with lessthan 10 percentinterlayered montmorillonite) with a 10 angstromperiodicitythat is relativelyunaffected by heatingto 550øC for 1 hour and glyclolation, to a randommixed-layer illite-montmorillonite with up to 45 percentmontmorillonite layers. The mixed-layer illite-montmorilloniteyields X-ray reflectionssimilar to those reportedby MacEwan (8, p. 167). This includesa reflectionat about30 angstroms withoutintegralsub-orderreflections.This phenomenon hasbeen interpreted(14, p. 217; 8, p. 167) asdueto somestatistical regularitywithin a long sequence of layers. HYDROTHERMAL ALTERATION IN DRILL HOLES 1417 Away from zonesof intensealteration,mixed-layerillite-montmorillonite with a largepercentage of montmorillonite layersis the abundantclaymineral. As zonesof intensealterationare approached,the percentageof montmorillonitelayersdecreases. In the zonesof intensealterationillire with lessthan 10 percentinterlayeredmontmorillonite is the only clay mineral. Theseconclusions,derivedfrom X-ray diffractograms of highlyalteredand lessaltered piecesof core, are corroboratedin thin sectionsby a general increaseof the lowestindex of refractionof the mixed-layerillite-montmorillonite with more intense alteration. Although the changefrom mixed-layer illite-montmorilloniteto nearly pure illire seemsto be continuousin the samplesstudied, two apparently distinctphasesare indicatedby X-ray diffraction in somesamples. Therefore, illite and mixed-layerilIite-montmorillonite are representedby separate fieldsin Figure 2, but the short-dashed boundarybetweenthem indicatesour uncertaintyof the nature of the difference. The upper part of drill hole GS-3 passesthrough hot spring sinter and arkosicalluvium. Some of these rocks were altered in the past by strong sulfuricacid solutionspercolatingdown from the then-existingsurfaceto the water tablein existenceat that time. The sulfuricacid was formedby oxidation of hydrogensulfidegasthat separatedat the water tablefrom the rising springwaters. Similar acid conditionsexist locallytoday on the Main Terrace, particularlyadjacentto fissures,and an outstandingexamplehas been described from GS-7 drill hole in the Silica Pit area I mile west of the Main Terrace (12). The silicioussinter depositsconsistentirely of amorphousopal at the surfacebut increasingamountsof/•-cristobalite (high cristobalite)occurat depth,formedby crystallizationof opal. The /•-cristobaliteis distinguished by a strongX-ray peaknear4.10 angstroms. Arkosicalluviumconsisting of disintegratedgranodioriteand fragmentsof volcanicand metamorphicrocks is composeddominantly of quartz, K-feldspar, and plagioclase.Where leachedby acid the alluvium containsquartz, kaolinite,/•-cristobaliteand small amountsof pyrite, illire and rarely alunite. For the purposeof examiningthe alterationeffectof risingwaterson the rocks,the near-surfaceacid leachedzone must be ignored. Drill Hole GS-4.--The mineralogyof drill corefrom GS-4 is plottedon Figure 3. The observedmineralsand the pattern of alterationis similar to that of GS-3. However,becauseGS-4 intersectsmany closelyspacedfracturesrelatedto the easterlydippingmain zoneof fissuresthat controlup-flow of thermalwaters (Fig. 1), the rock masshas beenmore pervasivelyaltered. This is indicatedin Figure 3 by the virtual absenceof biotite and replacement calciteand the relative abundanceof pyrite, hydrothermalquartz, and illite with little interlayeredmontmorillonite. Original plagioclaseis relatively rare in GS-4, andmuchchloritethat replacedbiotitehasin turn beenreplaced pseudomorphically by white mica. An anomaloussituationis found near the bottom of GS-4. Intensely alteredcorefrom a depthof 476 feet containingillite, quartz,and pyrite is devoidof K-feldsparand yet containsabundantalbiticplagioclase.A similar 1418 R. SCHOENAND D. E. WHITE situation occurs at a depthof 505feetalthough K-feldspar andchloriteare notcompletely replaced.Theretention of plagioclase in theintensely altered zoneof sericitization hasnotbeennotedelsewhere at Steamboat Springs. CEOCaE•STR¾ OF A•-TER.•0N Twenty-five rockanalyses madeby standard rapidmethods (10) were available for studyof therocksfromGS-3andGS-4. Analyses recalculated to constantrock volumeshowthat K20, S, H20, and someCO2 are added duringalteration,and SiOn,Na=O, and someCaO are lost. The lossesand gainsof thesechemical components canbe relatedin detailto thechanges in mineralogypreviouslydescribed. 'Hornblende, the mineralmostsusceptible to alteration, is replaced by mixed-layer illite-montmorilloniteand iron-rich chlorite. Sodium and cal- ciumprobably first go into montmorillonite and theninto solutionduring alteration andareremoved fromtherock. Somecalcium formscalciteduring this initial stageof alteration. Chlorite,whichtypicallyoccursin pseudomorphic replacement of biotite, is green and pleochroicand generallyexhibitsan anomalousbrown interferencecolor. However,interference colorsfrom somechloriterangefrom anomalousblue up to first order red. The chloriteflakeswith red interference colorsare length-slow andare interpreted to be iron-rich(1). Presumably potassium and silicaand possiblysomemagnesium are lost and water added during the alterationof biotite to chlorite. The releasedpotassiumis probablyfixednearbyin mixed-layer illite-montrnorillonite that is replacing plagioclase feldspar. Analysesindicatethat the illite is phengiticwith the magnesiumpresumablyderivedfrom biotite and hornblende. The alterationof plagioclase feldsparto mixed-layerillite-montmorillonite andcalcitefollowsthe oftenobserved patternof greatestinstabilityfor calcic plagioclase followedin the mostintensealterationby the moresodicplagioclase. Silica,calcium,and somesodiumare releasedas productsof this alteration. The mostintensealterationobservedin GS-3 and GS-4 producesillire from mixed-layerillite-montmorillonite by the fixationof potassium from the hydrothermalfluid. K-feldspar also alters to illire in this environment. The pseudomorphic replacementof chlorite by coarse-grained white mica (sericite) releasesiron which combineswith sulfur from solutionto form pyrite. This causesan inverserelationshipbetweenchlorite and pyrite. Direct replacementof biotite by sericite,without an interveningstageas chlorite, has not been demonstrated. Silica is releasedto solutionduring the alterationof all the primary silicateminerals andchlorite. Analyses indicate thatintense alterationslightly reducesthe amountof SiO• in a rock,but figures2 and 3 showthat quartz increases considerably in the intenselyalteredrocks. This paradoxcan be explainedby the fact that about75 percentof the freshgranodioriteis composedof mineralsthat yield somesilicato solutionduring alteration. Much of this silicaprecipitatesin the intenselyalteredrocksadjacentto veins,thus HYDROTHERMAL ALTERATION IN DRILL HOLES 1419 explainingtheir higher quartz content. But somesilica escapesfrom the rock either to precipitatein the veins or to be carried off in the rising solutions. This lossof silicaexplainsthe lower SiO2 contentof rocksfrom the most intenselyaltered zone. The patternof alterationobservedin GS-3 and GS-4 is very similar to that reportedfrom Butte, Montana (9). At Butte, mild alterationyieldsa zone of montmorilloniteand chlorite,and intensealterationdestroysall original and early hydrothermalmineralsand yields sericite,pyrite, and quartz. However, at Butte thesetwo zonesare separatedby a zonein which montmorillonite and chlorite are converted to kaolinite. In GS-3 and in GS-4, no intermediate kaolinite zone is found. Comparisonof the mineralogyof GS-3 and GS-4 with GS-1, 2, 5, and 7, describedby Sigvaldason and White (11, 12), indicatesgenerallygood agreement.The agreementis especiallygood for GS-5, which is on the Main Terrace425 feet north of GS-4. The kaolinitereportedat depthin GS-1 on the Low Terracemay be equivalentto the intermediatekaolinitezone of Butte. We donotyet understand why kaoliniteis developed soextensively in the Low Terrace, apparentlyunrelatedto oxidationof H2S above the watertable,butis absentin thedeepalterationof the Main andHigh Terraces. The mineral assemblage illite-quartz-pyrite,found in the sericiticzone immediately adjacentto fractures,is inferredto be in stableequilibriumwith the deephydrothermalfluid that movedupwardalong the fractures. The composition of this fluid can be inferredfrom experimentaldata on aqueous fluidsin equilibrium with illite andcanbe compared with present-day hydrothermal fluids of the SteamboatSpringssystem. At the temperatureof the rocksin the lower part of the drill holes(about 170ø C), illite wouldbe stablein a solutionwhosemolal ratio of K + to H* was between108'4and 10•'• in the presenceof quartzand at a total pressureof 1,000 atmospheres.These valuesare extrapolatedfrom the experimental data.Hemleygot from 200øC to 500øC (6 p. 548, and 5, p. 245). The effect of the much lower pressurein the drill holes (from 10 to 25 atmospheres)is presumablyto movethe stabilityfield of illite to slightlylower K*/H* ratios. An average valuefor K* in watersfromdrillholesGS-3,4, and5 is 65 ppm or a molalityof 1.67 X 10-8. Water at depth,with all CO2 in solution,has about650 ppm total CO•.. Thermodynamic calculations basedon theoretical valuesfor thedissociation constants of H2COaat hightemperature(4) indicate a molalityof H* of 7.94 x 10-* for this waterat 170ø C. Thesecalculations take into accountthe activitycoefficients of the hydrogenand bicarbonateions at 170ø C. The effect of sodiumnot balancedby chloride,which must be balancedby bicarbonate, is also includedin the calculations.Using these valuesthe K*/H* molal ratio of the present-day thermalwatersat depth is 10TM. Thisvalueliesin thekaolinitestabilityfieldcloseto theextrapolated boundarybetweenkaoliniteand illite. However,the effectof lowerpressm'e wouldplacethis K+/H" valueslightlywithin the illite stabilityfield. Similarly,the calculatedlga*/H* molal ratio in the present-daythermal watersis 104'*,a value alsolying in the extrapolatedkaolinitestabilityfield 1420 R. SCHOEN AND D. E. WHITE but closeto the boundarybetweenkaoliniteand montmorillonite (6, p. 549). The effect of lower pressurewould be to favor the formationof montmorillonite over kaolinite. However, montmorilloniteis not found closeto frac- tures,whichmustmeanthat the Na+/K+ ratio in the hydrothermal fluid is not high enoughto make stablea sodium-richphase. The fact that montmorillonite becomes a larger proportionof the mixedlayer clay with increasingdistancefrom the fractures, indicatesthat the Na+/K + ratio of pore fluidsis increasingaway from fractures. This increase in Na+/K + is causedby: a decreasein K + due to the formationof illite in the sericiticzone, and an increasein Na+ due to the breakdownof plagioclase feldspar. Orthoclase,the dominantpotassium-rich mineralin the fresh rock, doesnot break downuntil it is encroached on by the sericiticzonewhere it providesK + to the pore fluids, and results, perhaps,in a slightly higher t(+/H + ratio than in the adjacentfracture. Therefore, becauseillite appearsto be a stable phasein the most altered rocks of drill holesGS-3 and GS-4, and becausethe water presentlyin the spring systemhas a calculatedcompositionin which illite shouldbe stable, we concludethat the present-dayspring waters are producingthe observed hydrothermalalteration. This hypothesis, coupledwith the provenability of thesewaters to depositmetals,'indicatethat the spring waters are similar to fluidsthat haveformedsomeore deposits. ACKNOWLEDGMENTS Theauthors benefited fromdiscussions ofthecalculation ofhydrogen ion concentration at elevatedtemperatures with: G. G. Ehrlich, I. Barnes,W. L. Polzer, and J. J. Hemley. Critical review was graciouslyprovidedby ]. ]. Hemley and L. J. P. Muffler. U.S. GEOLOGICAL SURVEY, MENLOPARK,CALIFORNIA, Jan. 20, 1965 REFERENCES 1. Albee, A. L., 1962, Relationshipsbetweenthe mineral association,chemical compositionand physical properties of the chlorite series: Am. Mineralogist, v. 47, p. 851-870. 2. Brannock, W. W., Fix, P. F., Gianella, V. P., and White, D. E., 1948, Preliminary geochemical results at Steamboat Springs, Nevada: Am. Geophys. Union Trans., v. 29, p. 211-226. 3. Chu, T. Y., Davidson, D. T., and Sheeler, J. B., 1954, Mathematical analysis of a layer extraction method for separating clay-size material from soils: Clays and Clay Minerals; Proc. 2rid Nat. Conf., NAS-NRC pub. 327, p. 462-479. 4. Ellis, A. J., 1955, Effect of temperature on chemical equilibria in geothermal chloride water: Ninth Geothermal Chemical Rept. of the New Zealand Dept. of Scientific and Industrial Research, 8 p. 5. Hemley, J. J., 1959, Some mineralogical equilibria in the system K•O-AlaOa-SiO•-H•O: Am. Jour. Sci., v. 257, p. 241-270. 6. Hemley, J. J. and Jones, W. R., 1964, Chemical aspectsof hydrothermal alteration with emphasis on hydrogen metasomatism: EcoN. G•ot.., v. 59, p. 538--569. 7. LeConte, Joseph, 1883, On mineral vein formation now in progress at Steamboat Springs comparedwith some at Sulphur Bank: Am. Jour. Sci., v. 25, p. 424--428. 8. MacEwan, D. M. C., 1956, A study of an interstratified illite-montmorillonite clay from Worcestershire, England: Clays and Clay Minerals; Proc. 4th Natl. 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