itaya et al_1996 gca argon alunite

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    TABLE I. Alunite samples investigated in this study

    Sample no.Depositand Genetic

    location environmentSample description,

    occurrenceDeposit age Sampte preparation,

    size fraction

    AAR3(8-5) Riaza alunite-kaolinite deposit,central Spain

    MAD/FM Kiraly Hill kaolinite Steam-heateddeposit, Mad,southern TokajMtns, Hungary

    AK92/A19 Akahvahigh- Magmatic-sulfidation hydrothermalepithermaldeposit, centralHokkaido, Japan

    ALRDG/CG Alunite Ridge Magmatic-alunite deposit, steamsouthwest ofMarysvale, Utah

    F in e-gr ained rhombohedral 13.5alunite with associated halloysite- 13.9kaolinite; as porcelaneous veins, pods,and large replacement deposits inSilurian black shale

    Rhombohedral crystals in kaolinite-richaltered zone associated withepithemtal Auquartz veins andsilicasinter or silicified sediments; alteredMiocene andesitehost rock

    Coarsely crystalline, tabular or bladed 9.7pink alunite with dickite. diaspore,pyrophyllite and zunyite in theadvanced argillic zone that surrounds

    Au-mineralized vuggy silica; asreplacements orfissure and cavityfilling in Miocene andesite

    Plumose aggregates oflight pink alunite 13.6 0.6crystals up to 1 cm long, in massive 14.3 0.6aluntte veins up to 20 m wideand 100 mdeep; crosscutting Oligoceneintermediate composition volcanic rock

    5.2

    4.7

    23.1

    -2.0

    Alunite crystals or crystafragments, 5 to 6 sizfraction

    25 to 50 mesh crystals ocrystal fragments, treatto removeFe oxide andhydroxide coatings

    25 to 50 mesh crystals ocrystal fragments, treatto removeFe oxkle andhydroxide

    25 to 50 mesh crystals ocrystal fragments

    same as above, treated dilute

    1

    *

    By previous studies, seeTable 3 for alunite ages determined in this study

    3

    Ages byE. H. McKee (USGS, written comm.. 1991) on and size fractions, respectively

    4

    No ages were available for Hill, but K-Ar ages for similar deposits km west of Kiraly Hill range between 10.4 and 10.9 Ma

    5

    Fe oxide treatment: reaction et during5 mins ofup to 1 g ofsample with4 ml 0.3MNa citrate, 0.5ml 1M Na bicarbonate and0.1 g Na dithianke

    HF treatment: reaction at room temperature during 12Omins of 0.6 g ofsample with 100 ml of concentrated hydrofluortc acid: distilled

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    F I G. 1. Scanning electron images of typical tine-grained rhombohedral alunite of supergene origin (A. scale bar

    = 10 and coarse-grained tabular and bladed alunit e of magmatic-hydrothermal origin (B. scale bar = 500

    Samples from the Riaza alunite-kaolinite deposit. central Spain. and Akaiwa high-sulfidation epithermal deposi t.

    central Hokkaido. Japan. respectively.

    cristobalite diaspore dickite goethite, halloysite. hematite. i l l i t e ,

    jarosite, kaol ini te quar tz pyrophyllite smectite sulfide minerals

    ( mainly pyr i te)native sulfur, woodhouseite-svanbergite. and zun-yite Alunite is rarely the pure potassium endmember. and partial

    substitution of Na for K (up to greater than 95 Na) IS common

    in all alumte forming environments (Stoffregen and Cygan. 1990).

    Other spec ie s that may subs ti tu te for K inc lude ammonium

    Altaner et al.. 1988). hydronium Ripmeester et al.,

    1986. Alpers et al.. 1992). and or which may be

    accompanied by substitutionof for (Stoffregen and Alp-

    ers, 1987. Li et al.. 1992)

    The effect of alunite sample impurities on K-Ar analysesisvari-

    able It may be of limited significancei f there i s little substitution

    ofNa forK ( K content up to 9. 4 wt%) and the contaminant phasesare non K-bearing minerals such as quartz or kaolinlte. It may be

    problematic however, if the contaminant i s illite ofsignificantly

    older age (e g . old detrital illite mixed with young impure aluni tei n hypersalinelakesof southern AustraliaBird et al.. 1990; Alpers

    et al.) 1992). ori f the sample contains alunite or Jarosite of different

    ages (e g , older hydrothermal alunite partly replaced by younger

    superggene alumte and Jaroslte at the Goldtield. Nevada. high-sulfida-

    tion eplthermal Au deposit: Keith et al.. 1979: Vasconcelos et

    these cases preparation of mineral separatesof high purity

    is of great Importance to obtain reliable results. In our experience.

    the most significant step in obtaining pure alunite separates i s collec-

    tion in the field of the best possible specimens In the case of hypo-

    gene alunl te in ore deposits, this commonly implies collection of

    samples from drill core, below the oxidation zone In areas with

    supergene or steam-heated alteration the best specimens are com-

    monly found in powdery to porcelaneous veins or cavity-fillings.

    The minerals associated with alunite mentioned above are typi-

    callyfine graIned and Intergrown. Sample preparation method\ based

    on physical properties such

    specified gr av it y magnetic susceptibil-

    i ty or shape a r e therefore. of limited use The most effective meth-

    ods involve taking advantage of differences in particle size and

    chemically removing contaminant phases. A summary of these meth-

    ods is provided in Table 2. The samples selected in this study were

    all of high initial purity and required minor sample preparation.

    This consisted mainly of separation of individual crystals or Crystal

    clusters, light crushing, when necessary to reduce grain size, and

    sieving to extract the 25-50 mesh fraction (-0.7 to 0.3 mm. respec-

    tively: Table I ). The supergene alunite sample analyzed (AAR3 )corresponds to a 5-8 km size fraction prepared by elutriation and

    centrifugation to remove minor amounts of very fine (

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    45.30 T. I taya A. Arribas, J r , a nd T Okada

    0.1

    0.01

    1000

    100

    0.1

    0

    Temperature

    0.1

    0.01

    10

    1

    0.1

    2. Argon release patterns of samples investigated in this study (A-E), including data for analytical blanks See Table for sample information and Tables Al and A2 in Appendix for results of individual measurements.

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    m e n t a l of II

    J. and E.

    and text ures : tie of

    P. H.. T. A.. and PR . of

    to the of

    and West Africa.

    D . Rve R. P. and A

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    of by up to

    TABLE I. Step-heating argon isotope data for samples investigated in this study

    338.8+-4.o

    369.4 3.6 026

    0.03

    TABLE I. Continued

    266.9 5 .0 4.11 0.05

    14.53

    A2. Step-heating argon isotope forblanks