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    JOURNAL OF PETROLOGY VOLUME 38 NUMBER 3 PAGES 371391 1997

    Characterization and Origin of Aluminous

    A-type Granites from the Lachlan Fold Belt,Southeastern Australia

    P. L. KING1, A. J. R. WHITE2, B. W. CHAPPELL1 AND C. M. ALLEN1

    1DEPARTMENT OF GEOLOGY, AUSTRALIAN NATIONAL UNIVERSITY, CANBERRA, A.C.T. 0200, AUSTRALIA

    2VIEPS, DEPARTMENT OF EARTH SCIENCES, MELBOURNE UNIVERSITY, PARKVILLE, VIC. 3052, AUSTRALIA

    RECEIVED APRIL 22, 1996 ACCEPTED OCTOBER 9, 1996

    The metaluminous to weakly peraluminous A-type granites of the INTRODUCTIONLachlan Fold Belt are a distinctive group of igneous rocks, on the

    Rock classification schemes are useful, not only for char-basis of chemical and mineralogical criteria. Those granites that

    acterizing rocks, but also because they potentially bringcontain ~6572% SiO2 can be distinguished from other types on us closer to understanding fundamental rock-formingthe basis of higher abundances of Fetotal/(Fetotal+ Mg), high processes. One of the most common methods of defining

    field strength elements, trivalent rare earth elements, Ga and Zn.granite types is in terms of mineralogical and/or chemical

    Mineralogically, they contain Fe-rich hydrous mafic minerals andcompositions, which are measurable and non-genetic

    primary ilmenite, and hence are reduced relative to the NiNiOparameters (e.g. cordierite granite, peraluminous granite).

    buffer. However, the extremely felsic A-type granites (SiO2 > ~72%)A chemicaltectonic approach to granite classification

    have the same chemical and mineralogical characteristics as felsic, has been taken by some researchers, where chemicalfractionated I-type granites. Recent analyses indicate that the Lachlan

    parameters are taken as indicative of the tectonic en-Fold Belt A-type granites have Sc, F, alkali element, trace transition

    vironment in which the granite formed (e.g. Pearce et al.,element and H2O contents similar to those of other unfractionated1984). Others have inferred magma source compositionsI-type granites. RbSr and NdSm isotopic compositions arefrom chemical and mineralogical features, for examplehighly variable, probably reflecting source region heterogeneity. Thethe I- and S-type classification of Chappell & Whitemetaluminous to weakly peraluminous A-type granites of the Lachlan(1974, 1992). The proliferation of classification schemesFold Belt are distinct from peralkaline rocks in terms of chemicalhas been reviewed by Clarke (1992) and Pitcher (1993),composition, petrography and field associations, although these rocksand reflects both the difficulty of choosing definitivehave been grouped together as a single type in current classificationcriteria for classification and the complexity of granites.schemes. We propose that the metaluminous to weakly peraluminous

    The term A-type was proposed in an abstract byA-type granites, such as those of the Lachlan Fold Belt, should beLoiselle & Wones (1979) to distinguish mildly alkalinedefined as aluminous A-type granites and should not be grouped

    rocks (high K2O + Na2O) from typical calc-alkaline (I-with peralkaline granites. The Lachlan Fold Belt aluminous type) rocks. Other distinctive features that those workersA-type granites have relatively high calculated zircon saturationproposed were high ratios of Fetotal/(Fetotal + Mg) andtemperatures. We suggest that these granites were produced by high-F/H2O ratios, high abundances of high field strengthtemperature partial melting of a felsic infracrustal source.elements (HFSE) and trivalent rare earth elements

    (REE3+), and low abundances of FeMg trace elements

    (Cr, V, Ni, Cu), Ba, Sr and Eu. Loiselle & Wones

    (1979) included peralkaline, metaluminous and weakly

    peraluminous rocks in their A-type group. In addition,

    they noted that A-type granites are characterized byKEY WORDS:A-type granite; aluminous A-type; peralkaline; Australia

    Corresponding author. Present address: Department of Geology, Box

    87-1404, Arizona State University, Tempe, AZ 85287-1404, USA. Oxford University Press 1997

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    JOURNAL OF PETROLOGY VOLUME 38 NUMBER 3 MARCH 1997

    Fig. 1. Map showing the location of the I-, S- and A-type granites in the Lachlan Fold Belt, along with andalusite to sillimanite grademetamorphic rocks, gabbros and bimodal rift complexes. The A-type granites have a wide distribution and make up ~06% of the granites

    exposed in the belt. The names of the granite units are given in Table 1.

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    KING et al. ALUMINOUS A-TYPE GRANITES

    Such complexities imply that although A-type granites alteration, typical of intrusive rocks, is common, withsecondary minerals including chlorite, muscovite, fluorite,commonly form late in a tectonic and magmatic cycle,

    that is not always the case; therefore anorogenic cannot epidote, sphene, siderite, magnetite, hematite, stilp-nomelane and amorphous iron oxides.be used as a general term to characterize these rocks.

    Also, the term anorogenic is used with various meanings. Enclave types in the A-type granites of the LFB haveabundances that are suite-specific. Granites of the GaboSome workers have applied the term anorogenic mag-

    matism to magmatism postdating major episodes of gran- Island and Mumbulla suites contain rare enclaves, xeno-crysts and phenocrysts. In contrast, the Wangrah Suiteitic magmatism (e.g. Bonin et al., 1978). Other workers

    define orogeny to include both magmatic and structural contains phenocrysts, rapakivi texture and microgranularenclaves, with considerable textural heterogeneity at allactivity. Furthermore, it can be difficult to constrain an

    orogeny to a specific time period, owing to lateral vari- scales.ations in the intensity of structural activity within aterrane, some of which may result from orogenic activityin adjacent terranes (e.g. the LFB and New England

    CHEMICAL COMPOSITIONSFold Belt; Chappell, 1994).Chemical compositions of 13 selected LFB A-type gran-ites and the average composition are listed in Table 2.Major element data were obtained by X-ray spectrometry

    PETROGRAPHY using fused discs (Norrish & Hutton, 1969). The traceelements Rb, Sr, Ba, Zr, Nb, Y, V, Ni, Cu, Zn, Ga, As,In the LFB, A-type granites are commonly pink, owingSn and Pb were measured on pelletized powder samplesto abundant brick red K-feldspar, but creamwhite K-using the X-ray spectrometric methods described byfeldspar is also present (Wangrah, Ellery and MongaChappell (1991). Instrumental neutron activation analysissuites and the A-type granites of the Wyangala Batholith).(Chappell & Hergt, 1989) was used to determine Cs, Hf,Plagioclase is normally zoned (commonly An4015) and noREE, Sc, Cr, Co, Th and U contents. Wet chemistrycores with higher anorthite contents have been identified.techniques from Peck (1964) were used to determine FeOAs with other near-surface granites, quartz occurs ascontent. Comprehensive chemical data for the Gaboembayed bipyramidal crystals in some rocks and quartzIsland and Mumbulla suites were previously given byfeldspar intergrowths are common. In many of the gran-Collins et al. (1982). On the basis of petrographic in-ites, quartz and feldspar proportions are close to near

    vestigations and the techniques described by Chappell &minimum-temperature melt compositions for pressures White (1992), no altered samples are included in the dataof 100200 MPa. All A-type granites of the LFB contain

    presented.annite and the majority contain small amounts of am-phibole. Amphibole compositions are summarized inTable 1. The crystal habits of mafic minerals tend to be

    specific to individual plutons. Both annite and amphiboleOXYGEN FUGACITY AND VOLATILEare observed as anhedral and euhedral crystals and areCONTENTSfound interstitially, individually, and in mineral ag-

    gregates. Annite rarely pseudomorphs Fe-rich amphibole. Ilmenite, typically found within mafic minerals, is theNotably, in the LFB, the aluminous A-type granites most common FeTi oxide mineral in the LFB A-type

    never contain pyroxene or olivine, although some Ba- granites. Ourdata indicate that the hematite andMnTiO3rich A-type volcanic rocks contain pyroxene. This differs components in ilmenite are very low (generally

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    Table2:ChemicalanalysesofA-typegranitesfromtheLachlanFoldBelt

    Averageof55

    AB412

    GI1

    AB239

    WB140

    BG20

    BG15

    AB422

    VB203

    AB421

    AB118

    AB238

    AB401

    WB121

    A-typesamples 1

    wt%

    SiO2

    7383

    245

    7045

    7360

    7095

    7206

    6985

    7192

    7253

    7587

    7532

    7700

    7638

    7667

    76

    69

    TiO2

    028

    016

    054

    038

    050

    025

    052

    024

    037

    013

    015

    015

    018

    009

    0

    06

    Al2O3

    1279

    066

    1326

    1272

    1317

    1319

    1377

    1354

    1308

    1229

    1271

    1183

    1214

    1210

    12

    60

    Fe2O3

    084

    046

    093

    199

    161

    056

    072

    064

    088

    088

    051

    040

    081

    060

    0

    34

    FeO

    154

    084

    332

    082

    228

    192

    314

    217

    171

    050

    116

    105

    078

    038

    0

    62

    MnO

    005

    002

    008

    004

    005

    005

    005

    006

    005

    003

    006

    004

    002

    002

    0

    03

    MgO

    029

    023

    061

    020

    046

    019

    091

    027

    048

    014

    023

    004

    009

    005

    0

    04

    CaO

    104

    055

    193

    083

    146

    119

    209

    152

    131

    070

    090

    061

    029

    053

    0

    54

    Na2O

    342

    033

    339

    362

    348

    352

    283

    325

    332

    380

    336

    306

    316

    325

    4

    16

    K2O

    467

    043

    398

    411

    416

    527

    465

    490

    488

    460

    461

    498

    513

    512

    4

    60

    P2O5

    007

    006

    018

    008

    011

    004

    019

    008

    012

    002

    005

    002

    005

    270 p.p.m.); both defined by Chappell & White (1992). Complete analyses of WB140, WB121 andthe LFB A-type average are given in Table 2.

    identified using the more mafic members (Whalen et al.,COMPOSITIONAL COMPARISON1987; Chappell & White, 1992).

    WITH I-TYPE GRANITESIn the case of discriminating the A-type granites from

    Many felsic, highly fractionated I-type granites have other granites we are principally concerned with I-typecompositions that overlap those of the intrinsically felsic rocks. A-type granites can be easily discriminated from

    A-type granites. When dealing with the more felsic gran- S-type granites because the latter have much higherites, there are difficulties with most genetic schemes,

    P2O5, lower Na2O contents, and show increasing P2O5mainly because such rocks tend to be close to haplogranite

    with fractionation, which contrast with A-type trends(near minimum-temperature melt) compositions. Thus,

    (Chappell & White, 1992). The felsic S-type granites

    felsic granites typically have converging major element are always peraluminous and become strongly so withcompositions and similar mineral compositions, with

    fractionation (two-mica granites), thus mineralogical cri-quartz and two feldspars occurring in subequal amounts

    teria alone will distinguish the two types.(Table 3). This immediately leads to problems; for in-Collinset al. (1982) and Whalenet al. (1987) comparedstance, classification schemes dependent on mineralogy

    the Gabo Island and Mumbulla A-type suites with otherbecome meaningless for the more felsic rocks (SiO2 >granites, and in doing so created classification criteria72%). The so-called alkali-feldspar granites are a goodthat many workers use to distinguish A-type character.example of this: Pitcher (1993) suggested that these areLandenberger & Collins (1996) similarly compared dataA-type rocks, whereas other workers have demonstratedfrom I- and A-type granites from the Chaelundi Complex,that some are I-type (MacKenzie et al., 1988, 1990). ToNew South Wales, Australia. We now have a largeruse chemical classification schemes when dealing withdatabase of LFB granites (1939 analyses with SiO2>57%)felsic rocks it is necessary to use distinctive granite as-

    sociations where the granite type can be most readily that allows us to better describe the compositional effects

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    Fig. 4. K2O vs Na2O for I-type and A-type granites of the Lachlan Fold Belt. Both K2O and Na2O increase with increasing SiO2 content forboth granite types; thus high K2O + Na2O is a characteristic of both I- and A-type felsic granites. It should also be noted that the A-type rocksare more potassic than sodic. Three extreme outliers of the I-type granites have not been included in the fields for the I-type granites. Theseare from the Urialla and Jungle Creek plutons (both 7075% SiO2; Na2O contents of 202% and 264%, and K2O contents of 378% and

    225%, respectively) and the Coles Bay pluton (Freycinet, >75% SiO2, Na2O and K2O contents of 491% and 371%, respectively).

    of fractionation in the LFB. As fractionation changes the Suite (average 73% SiO2) and Mumbulla Suite (average77% SiO2) granites have relatively high average Bacompositional features used for determining granite type,it is useful to undertake this kind of comparison. Average contents (767 and 575 p.p.m., respectively). In contrast,

    granites of the Wangrah and Yewrangara Suites havechemical data for the LFB A-type granites, and un-fractionated and fractionated I-type granites are pre- Ba contents that decrease from ~820 p.p.m. to ~40

    p.p.m., while SiO2 increases from ~70% to 77%. Basented in Table 3.Relative to typical I-type granites, LFB A-type granites contents in granites may reflect differences in source

    regions or pyroxene-dominated fractionation; however,have higher Fetotal/(Fetotal+Mg), although compositionalconvergence occurs for the most felsic rocks. This feature we currently do not fully understand the variations that

    are observed. Sr and Ca levels are generally lower in thecould be a function of the relatively reduced nature of A-type magmas. The LFB A-type granites are not unusually A-type than the I-type granites ( Table 3).

    Zirconium content is relatively high (commonly >300alkaline compared with other granites with similar silicacontents; as Na2O + K2O increases with SiO2 content p.p.m.) in the less felsic A-type granites (6572% SiO2)

    and decreases with fractionation in both the A- and I-in any granite suite these elements are not diagnostic(Fig. 4; Table 3). The LFB A-type granites are only type granites (Fig. 5; Tables 2 and 3). Y and Nb are alsorelatively abundant in the less felsic A-type granites, butclearly more K2O rich than the I-type granites at SiO2

    contents of 6570%. At higher silica contents, the A- show no clear trends with fractionation, while in theI-type granites those elements generally increase withtypes are weakly peraluminous as a result of fractionation.

    The perception that A-type granites are extremely fractionation (Table 3). Zn decreases with fractionationin both granite types, but average Zn content for A-typealkaline seems to have arisen from the convenient as-

    sociation of the letter a with alkaline, although A- granites is higher than that observed for the most felsicI-type granites. Thus, Zn is an indicator of A-type char-type granites were originally defined as mildly alkaline

    (Loiselle & Wones, 1979) or somewhat alkaline (Collins acter, but not a complete discriminant. Ga does not varygreatly with fractionation in the A-type granite suiteset al., 1982).

    Ba contents appear to be suite-specific for both the A- from the LFB, except in the Yewrangara Suite, where itincreases (Table 3). However, Ga contents increase withand I-type granites in the LFB. For example, the Gabo

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    fractionation in many I-type granites, which results in fields on geochemical plots (compare with Whalenet al.,1987). In some cases, rocks may plot in the A-type fieldGa/Al trends that can be readily discerned from theof one chemical discrimination diagram, but will not plotmajority of LFB A-type granites (Whalen et al., 1987).in the A-type field of another chemical discriminationThe REE behave similarly with fractionation in bothdiagram, owing to fractionation (e.g. the aluminousA- and I-type granites, although the more mafic A-typesubsolvus A-type rocks from Corsica; Poitrasson et al.,granites have flatter REE3+ patterns and much higher1994, 1995). In the absence of a close relationship withREE contents than typical I-type granites (Tables 2 andunfractionated rocks, distinction of strongly fractionated3). The LREE (LaSm) decrease with fractionation in

    A-type granites from similarly fractionated I-type granitesboth types. The most mafic rocks do not have a strongis difficult. At present, classification of very felsic rocksnegative Eu/Eu anomaly (e.g. Gabo Island and Mum-can only be made confidently when there is an associationbulla suites; Collins et al., 1982). However, Eu decreaseswith less evolved rocks within the same suite. Thus aas the rocks become more felsic, resulting in a strongsmall proportion of very felsic and fractionated rocks arenegative Eu/Eu anomaly (e.g. WB121), indicative ofambiguous in terms of I- or A-type character as a resultfeldspar fractionation. The HREE (GdYb) increaseof their prolonged evolution. Compositional separationslightly, or remain constant with fractionation in bothbetween the two types is very clear in less evolved rocks,the I- and A-type granites. Sample BG20 (Murrungowar)and mineralogical criteria can be used to discriminatehas strikingly different REE geochemistry from the otherthe types. Therefore, the A-type concept is valid.LFB A-type granites, with a steeper chondrite-normalized

    slope, and lower concentrations of HREE. We attribute

    these differences to BG20 being the most mafic rockanalyzed with annite as the sole mafic mineral (amphibole Granites problematic for classificationis present in all of the other less felsic compositions). As noted above, the extremely felsic granites are difficult

    The A-type granites of the Gabo and Mumbulla suites to classify using chemical data. Altered, felsic granitescontain high abundances of Sc (1418 p.p.m.), and high are even more problematic for classification and, as anSc was cited as a diagnostic feature of A-type granites example, we present data on the Freycinet and Housetopby Collinset al. (1982). However, the Sc content of other granites of Tasmania. These are felsic, strongly frac-

    A-type granites is variable and generally lies within the tionated (Rb > 270 p.p.m.) granites that are difficult torange observed for I-type granites of the same SiO2 classify as either fractionated I- or A-type granites. Theycontent. Within a particular SiO2 range, the average were designated I-type by Chappell et al. (1991) simply

    value for Sc in the A-type granites is slightly higher than because that is by far the more common type of granitethe average for the I-type granites and so, for this element, throughout the belt, although chemical compositionsthe average value is misleading and high Sc contents are overlap with those of A-type granites for some elementsnot diagnostic for LFB A-type granites. (e.g. Zr and Ce; Fig. 5). The Tasmanian rocks appear

    Low abundances of trace transition elements have also to be altered, on the basis of petrographic evidence, suchbeen cited as characteristic of LFB A-type granites by as an abundance of albitic plagioclase, and compositionalCollins et al. (1982), but this feature is also a reflection evidence (e.g. most have extremely low CaO abundancesof the inherently felsic nature of A-type granites; felsic I-

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    KING et al. ALUMINOUS A-TYPE GRANITES

    peralkaline rocks. Peralkaline rocks are unequivocally A- with the LFB aluminous A-type granites. The Narraburratype in this sense, whereas the metaluminous to weakly Suite rocks have much more variable Zr contents thanperaluminous A-type rocks are more ambiguous. We those observed for the LFB aluminous A-type granitescontend that there are distinctive features of the per- and some of them have substantially higher Zr contents.alkaline granites that are not shared with the aluminous World-wide, peralkaline granites commonly contain 1000

    A-type granites, such as indeed their peralkalinity, con- p.p.m. Zr (Eby, 1990), but contents as great as ~5000sequent distinctive mineralogy, characteristic field as- p.p.m. have been reported (e.g. Habd-Aldyaheen com-sociations and general chemical compositions. plex, Arabian Peninsula; Radain et al., 1981). This is

    Many of the peralkaline rocks are hypersolvus (with consistent with experimental evidence that Zr is morealkali feldspar the only feldspar) and the mafic minerals soluble in peralkaline than metaluminous melts (Watson,include fayalite, hedenbergite, aegirine, ferrorichterite, 1979). Zr content increases with fractional crystallizationriebeckite and arfvedsonite. These features indicate that in the peralkaline rocks if the magma reaches the granitethe peralkaline magmas had an anhydrous origin. In stage of fractionation at high enough temperatures andgeneral, the peralkaline rocks are associated with vo- the solubility of Zr has not been exceeded.luminous basalt, syenite and/or anorthosite. In contrast, The chemical trends observed for many peralkalinethe LFB aluminous A-type granites do not include any rocks could be achieved by Al2O3 depletion of either anhypersolvus rocks and those mafic minerals are not I- or A-type parent magma or basaltic magma by extremeobserved, excepting riebeckite, which is rare (Table 1). crystal fractionation of plagioclase and clinopyroxeneWe argue above that the LFB A-type granites have (Tuttle & Bowen, 1958) or Ca-bearing alkali feldsparnormal H2O contents and these petrographic ob- (Carmichael & McKenzie, 1963). These mechanismsservations support this proposal. In addition, the LFB appear consistent with peralkaline rock compositionsaluminous A-type granites are only associated with minor (H2O-poor, high Ba, Sr and HFSE, strong negative Eu/basalt and gabbros and never associated with syenite or Eu) and field associations (common mafic rocks), andanorthosite. have been proposed by many workers (e.g. Baker, 1974;

    Previous workers have discussed the differences be- Walsh et al., 1979; Turner et al., 1992).tween peralkaline and aluminous A-type rocks. Whalen The differences between the metaluminous to weakly& Currie (1990) studied large metaluminousperalkaline peraluminous A-type rocks and the peralkaline rocks arecomplexes, emphasizing the Topsails Complex, New- such that they should not be grouped together in rockfoundland. They suggested that those rock associations classification schemes. In grouping these two different

    have a diff

    erent petrogenesis from other smaller, highly types of granite together, Loiselle & Wones (1979) hadfractionated A-type granites. We contend that the metal- access to many fewer data than now available. The nameuminousperalkaline complexes differ from the smaller peralkaline should be retained for a group of rocks thatmetaluminousweakly peraluminous granites of the LFB have long been regarded as distinctive. The aluminousand that the latter rocks need not be highly fractionated. A-type granites of the LFB and elsewhere are differentIn other regions, metaluminous A-type rocks and the from peralkaline rocks, and as the two types are likelylarger peralkaline A-type rock associations have been to have different origins, it is inappropriate to groupgrouped together. For example, Eby (1992) divided A- them together. We recommend using the term aluminoustype granites from around the world into A1 and A2 A-type in reference to the LFB rocks and similar rocksgroupings on the basis of tectonic affiliations and the Y/ elsewhere. Retaining the A term is useful because ofNb and Yb/Ta ratios of the rocks. If a wider group of the extensive literature on those rocks using that name,trace elements are examined [e.g. the figures of Eby even though some A characteristics are not distinctive in(1992)], then compositions of the A1, A2, peralkaline and the LFB and probably elsewhere (e.g. extremely alkaline,

    metaluminous rocks overlap. This is due to the inherently anhydrous and anorogenic). Perhaps A should nowfractionated nature of many of the peralkaline granites, refer to anomalous in the LFB, in reference to thewhich leads to great compositional variation within a anomalously high HFSE contents of the aluminous A-suite. However, if the most mafic member of a suite is type granites (compare with Hogan et al., 1992).examined, the peralkaline rocks typically contain more

    Ba, Sr, HFSE and REE3+ and strong negative Eu/Euanomalies relative to metaluminous A-type granites. Wesubmit that these differences result from different pe-

    ISOTOPIC WORKtrogenetic schemes for the peralkaline rocks (fractionationIsotopic compositions were measured using a multi-from a mafic source; below) and the aluminous rockscollector VG354 thermal ionization mass spectrometer(partial melting of an infracrustal source; below).at the Centre for Isotope Studies, North Ryde, NewIn Fig. 5, we show some of the variation in Ebys A2

    group by comparing the peralkaline Narraburra Suite South Wales. For each analysis, a 100 mg sample was

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    Fig.

    5.

    (a)ZrvsSiO2

    forI-type,pera

    lkalineandA-typegranitesoftheLachlanFoldBelt.Theoutlinearbitrarilyencloses~98%

    oftheI-typegranites.TheI-typegranitesthathaveZr

    contents>300p.p.m.includetheBurrinjuckandYeovalgranites,whichbelongtotheBoggyPlainSupersuite(discussedintext;Wybornetal.,1987).Also,theGobonderyandYackandandah

    graniteseachhaveoneanalysiswith>

    300p.p.m.Zr.NoneofthosegranitesareconsideredtobeA-type,asothercriteriaarenotsatisfied.Itshouldbenotedthattheperalkaline

    Narraburra

    Granite(Wormald&Price,1988;Wormald,1991)hasextremelyvariableZrcont

    ents,withsomegraniteshavingveryhighcontents.

    TwoperalkalinerocksfromtheNarra

    burraSuite

    werenotplottedinthediagram(from

    theBoginderraGranite;Wormald,1991).ThoserockshaveZrcontentsof638and799p

    .p.m.,andSiO2contentsof7395and7548%

    .(b)Cevs

    SiO2

    forI-type,peralkalineandA-typ

    egranitesoftheLachlanFoldBelt.Theoutlinearbitrarilyencloses~994%oftheI-typegranites.TheI-typegranitesthatplotoutoftheoutlined

    areaincludetheBurrinjuckandJacksongranitesoftheBoggyPlainSupersuite(disc

    ussedintext;Wybornetal.,1987);alsotheJindera,MumbedahandButmaroogranites.Th

    osegranites

    arenotconsideredtobeA-typebe

    causeothercriteriaarenotsatisfied.Oneana

    lysisfromtheJinderaGranitewasnotplotted

    onthediagram(SiO2=

    7067%,

    Ce=

    422

    p.p.m.).

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    dissolved in an open beaker on a hot plate employing al., 1982; Clemens et al., 1986; Whalen et al., 1987;Peterson et al., 1991; Skjerlie & Johnston, 1992). OurHF, HNO3 and HClO4. Sr was separated using a one-

    step ion exchange column in a BioRad AG50W-X8 resin data indicate that other petrogenetic models are necessaryto explain the LFB A-type granites and possibly otherand dilute HCl. Sr isotopic compositions were corrected

    for mass fractionation with an 86Sr/84Sr value of 01194. aluminous A-type granites world-wide.Granites, as felsic rocks of minimum-temperature meltNd was extracted using a single column pass process (see

    Korsh & Gulson, 1986). Both Sr and Nd isotopic ratios composition, represent either products of fractional crys-

    tallization of quartz, feldspars and mafic minerals fromfor a single dissolution were collected at least 50 timessuch that 2 values were at most 00015%. Procedural a more mafic melt, or primary melts derived from a source

    containing quartz and feldspars. Within the constraintsblanks were 790 pg of Nd and 250 pg of Sm. For RbSranalyses, 10 runs of a standard (SRM987) gave 84Sr/ imposed by these two broad mechanisms, the distinctive

    features of the aluminous A-type granites could reflect86Sr = 00564895, 86Sr/88Sr = 0120182196, 87Sr/86Sr = 07102623. For Nd isotopic analyses, 27 dis- either a characteristic parent magma composition and/

    or source rock, or differences in the physical and/orsolutions of Onions standard gave 146/144Nd =0721396320 (2), 145Nd/144Nd = 03484072, chemical conditions of melting, magma separation or

    crystallization. We briefly review some of the arguments143Nd/144Nd = 05111122.Isotopic ratios are potentially useful indicators of gran- previously made for the genesis of I-type and peralkaline

    rocks, in the context of evaluating the potential geneticite source regions; however, in the case of the SmNdand RbSr systems, the A-type granites are ambiguous, schemes for the aluminous A-type rocks.

    as ratios overlap with those of I-type and peralkalinerocks (Table 4, Fig. 6). None the less, no sedimentarycomponent is indicated by isotopic data. The A-typeshave relatively high initial 143Nd/144Nd ratios with Nd

    values (at 400 Ma) varying from +501 to 315; thereInvolvement of a mafic magmais a range from mantle to crustal values. This variationFractional crystallization, generally of a mantle-derivedis consistent with Nd isotope heterogeneity in granitesmagma, to produce I-type granites or peralkaline com-from eastern Australia and from Corsica (Chappellet al.,positions has been proposed by many workers (e.g.1990; Turner et al., 1992; Poitrasson et al., 1994, 1995).Bowen, 1928; Baker, 1974; Walsh et al., 1979). AnIn both cases, isotope heterogeneity has been interpretedexample of such a process in the LFB is the I-type Boggy

    to reflect magma source region heterogeneity. These Plain Supersuite (Wyborn et al., 1987). Those rocks doresults illustrate some of the difficulties in applying Ndnot share the chemical features of the LFB A-types,isotopes to elucidate the genesis of extremely felsicexcept at their most felsic compositions, where we havemagmas, such as the A-type granites.seen that there is overlap between I- and A-type com-Calculated initial 87Sr/86Sr ratios (at 400 Ma) are inpositions. At the more mafic compositions, where A-typethe range 07002070888, excluding sample AB401.granite chemical features are distinctive, the fractionatedSample AB401 has extremely low initial 87Sr/86Sr that isgranites can be easily distinguished from the Boggy Plainthought to reflect an inaccurate age correction owing toSupersuite rocks. For example, Zr contents are generallythe very high Rb/Sr ratio. We do not consider that thelower in the Boggy Plain Supersuite because they areSr initial ratios are meaningful in the case of the LFBderived from a mafic magma that was undersaturatedA-type granites, owing to their relatively low Sr contentswith respect to Zr (exceptions are listed in Fig. 5). Onceand thus their high sensitivity to changes of Rb/Sr or SrZr becomes saturated in a magma, high Zr contentsisotopic compositions.

    cannot be reached via fractional crystallization, especiallyif zircon is one of the fractionated minerals and tem-perature falls during fractionation. A few granites do

    have high Zr contents in the Boggy Plain Supersuite(>300 p.p.m.; Fig. 5), but they are not considered to be

    PETROGENESIS A-type as other criteria are not satisfied.The LFB metaluminous to weakly peraluminous A-type One argument against a mechanism of fractional crys-

    tallization of a mafic magma to produce the aluminousgranites have chemical and mineralogical attributes

    which must reflect a somewhat different petrogenesis A-type granites of the LFB is that some of the least

    evolved rocks have Eu, Rb, Sr and Ba contents thatfrom typical I-type granites. Previously, the distinctivefeatures of the A-type granites, such as high HFSE and preclude extensive feldspar fractionation from a mafic

    source. The composition of the very felsic MumbullaGa, were explained in terms of high F, low H2O andhigh alkali element contents in the source (e.g. Collins et Suite rocks [high SiO2, ~77%; high Ba, 500655 p.p.m.;

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    Table4:RbSrandSmN

    disotopicdataforselectedA-typegranitesfromtheLachlanFoldBelt

    AB412

    GI1

    AB239

    WB140

    BG20

    B

    G15

    AB422

    VB203

    AB421

    AB118

    AB238

    AB401

    W

    B121

    87Rb/86Sr

    3309

    4778

    3522

    1449

    4562

    7617

    8323

    11231

    13416

    19510

    39443

    63068

    87Sr/86Sr

    0724632

    0736103

    0725114

    0716215

    0733704

    0745348

    0750039

    0763997

    0780686

    0815897

    0909173

    1067880

    SriT

    070579

    070888

    070505

    070796

    070772

    070196

    070263

    070002

    070426

    070476

    06845

    070864

    147Sm/144Nd

    011601

    0146

    02

    011856

    012091

    008441

    011893

    011419

    011854

    014442

    015022

    014056

    018877

    018412

    143Nd/144Nd

    0512527

    0512

    431

    0512331

    0512496

    0512223

    0512369

    0512540

    0512690

    0512500

    0512355

    0512350

    0512779

    0512681

    Ndo

    217

    404

    599

    277

    810

    525

    191

    101

    269

    552

    562

    275

    084

    InitialNdT

    051222

    0512

    05

    051202

    051218

    0512000

    051206

    051224

    051238

    051212

    051196

    051198

    051228

    051220

    SrT

    977

    1421

    872

    1289

    1

    254

    430

    526

    153

    760

    831

    2068

    1

    385

    NdT

    195

    146

    200

    110

    237

    128

    23

    501

    003

    315

    276

    315

    148

    ModelNd

    813

    1370

    1139

    904

    969

    1

    084

    779

    583

    1191

    1640

    1436

    1589

    1

    845

    ThesubscriptTreferstothevaluecalculatedat400Ma.

    Thesubscriptoreferstothein

    itialvalue.

    TheCHURvaluesusedwere14

    7Sm/144Nd=

    01966and143Nd/144Nd=

    0512638(Jacobsen&Wasserburg,

    1980

    ).

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    KING et al. ALUMINOUS A-TYPE GRANITES

    Fig. 6. Plot of Nd vs initial 87Sr/86Sr (both calculated for 400 Ma) showing the LFB A-type granites. Also shown are the fields for I- type and

    S-type granites from the LFB [data from Chappell et al. (1990)] and the field for peralkaline rocks from the Padthaway Ridge, South Australia(Turner et al., 1992). It should be noted that the A-type granites overlap isotopically with the I-type and peralkaline rocks. The sample AB401

    (Dunskeig pluton, Wangrah Suite) has been excluded from this plot, as explained in the text.

    moderate Rb, 225261 p.p.m.; and low to moderate Eu, Partial melting121168 p.p.m. (Collins et al., 1982)] indicates that Many workers have suggested that A-type granites arethere has been no appreciable feldspar fractionation. The produced by combined partial meltingfractionationmost mafic members of the Yewrangara and Wangrah from source regions of slightly different composition thanSuites (WB140 and AB412, Table 2) similarly have those for I-type granites (e.g. Anderson & Cullers, 1978;compositions that were probably not produced by frac- Cullers et al., 1981; Collins et al., 1982; Anderson, 1983;tionation from a mafic source, but appear to be the result Clemens et al., 1986; Whalen et al., 1987; Wormald &of partial melting.

    Price, 1988; Creaseret al., 1991; Landenberger & Collins,Magma mixing is a process that has been advanced 1996). Proposed source compositions that have beenby some workers to produce A-type granites (e.g. Bedard, favored are lower crustal, including tonalite, granodiorite,1990). However, as many of the intrinsically felsic A- peraluminous granulite, charnockite and granulitic re-type granites of the LFB are weakly peraluminous, very siduum from melting of I-type granites. On the whole,little strongly metaluminous mafic magma could have the researchers listed above have discussed granites withbeen added to the granite magma, especially considering similar compositions to the LFB A-type granites. Thethat the mafic magmas have higher concentrations of Al general approach has been to try and account for anand (Ca + Na + K). Also, magma mixing seems H2O-poor, F-rich source. These models, or any othersunlikely in the LFB, on the basis of the occurrence that invoke a distinctive source for the A-type granites,of bimodal A-type rock associations and the restricted have to be reconciled with the fact that A-type granites

    miscibility of the two magma types (Sparks & Marshall, may be adjacent to or intrusive into other granite types

    and, in the LFB, have a very limited distribution. This1986).

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    means that if the sources for A-type granites are dis- aluminous A-type granites such as those of the LFB. Thistinctive, then those source regions had to be either identification of aluminous A-type rocks has petrogenetic

    very localized and/or separated vertically from adjacent implications.granite source regions. (2) Aluminous A-type granites commonly have Fe-rich

    mafic minerals and primary ilmenite. The more mafic

    (~6572% SiO2) granites are distinguished chemically

    from I-type granites by relatively high Fe total/(Fetotal +

    Mg), HFSE (especially Zr, Nb, Y), REE3+, Ga and Zn.Synthesis

    The RbSr and NdSm isotopic compositions for theIn assessing the possible genetic schemes for the LFB A- LFB A-type granites overlap with those of peralkalinetype granites, the most important single feature is their and I-type granites from elsewhere.high Zr contents relative to the I-type granites, which, (3) More evolved A-type granites are difficult or im-as we have noted above, is related to higher calculated possible to distinguish from fractionated I-type granites.zircon saturation temperatures. Zr is an ideal discriminant To characterize any kind of felsic granite it is necessaryfor the aluminous, unfractionated LFB A-type granites. to compare suites of rocks in which less evolved rocksIn addition, its behavior in granite magmatic systems

    are also present. New data indicate that some featureshas been characterized experimentally (Watson, 1979;

    of LFB aluminous A-type granites, which were previouslyWatson & Harrison, 1983). We suggest that the otherconsidered diagnostic of the type, are actually similar to

    HFSE that are relatively abundant in the A-type granitesthose of many felsic I-type granites; for example, Na2Ohave partition coefficients that are similarly dependent+ K2O, Sc and trace transition element contents.on temperature.

    (4) The LFB aluminous A-type granites generally haveThe critical observation that A-type magmas existed

    reduced compositions relative to the NNO buffer, whichat higher calculated zircon saturation temperatures than

    most probably reflects the character of the source region.other felsic granites implies that they were derived from

    Our data also show that those granites do not have higha fertile felsic source region that required a high tem-

    F contents compared with fractionated granites. Thereperature before an extractable magma was produced.is no evidence that H2O contents are lower than for felsicWe favor a felsic infracrustal source that could overlap inI-type granites; thus the term anhydrous in referencecomposition with I-type sources, on the basis of similaritiesto the A-type rocks is misleading. These intensive para-between the two rock types. The major difference be-meters have a key role in the petrogenesis of this granitetween petrogenetic schemes for the aluminous A-typetype.magmas and the I-type magmas is that different physical

    (5) Calculated zircon saturation temperatures for al-conditions prevailed. Limited availability of H2O anduminous A-type granites are higher than those of otherrelatively low oxygen fugacity during partial melting, andgranite types. We suggest that the other HFSE that aretherefore high temperatures, may be all that is requiredrelatively abundant in the aluminous A-type granitesto produce aluminous A-type granites. As melt viscosityhave partition coefficients that, like Zr, are dependentis reduced at high temperatures, an extractable melt mayon temperature.be generated at smaller degrees of partial melting than

    (6) The term anorogenic is unclear and thus shouldneeded for other granite types. The necessarily highnot be used for characterizing A-type granites. Geo-temperatures required to produce an extractable magmachronological evidence suggests that LFB aluminous A-may have been initiated by mantle upwelling or mafictype granites can be emplaced at any time during amagma influx into a localized area. Although we cannottectonicmagmatic episode. In the LFB, aluminous A-rule out magma mixing as a factor in petrogenesis, theretype granites are found adjacent to I-type granites ofis no direct evidence to support it, therefore we do notsimilar age and have similar field relations.favor it.

    (7) We favor a petrogenetic scheme in which the

    aluminous A-type granites were derived by small degrees

    of partial melting of a felsic, infracrustal source region.

    The source region was probably relatively reduced, withCONCLUSIONS water and F contents similar to those of I-type source

    regions. The A-type source regions could be either very(1) The term A-type as proposed by Loiselle & Woneslocalized or separated from other granite source regions(1979) is too broad to succinctly define rocks world-wide.

    vertically in the crust. The necessarily high temperaturesWe recommend using the term aluminous A-typerequired to produce an extractable magma may havein reference to the LFB rocks and similar rocks else-been initiated by mantle upwelling or mafic magmawhere. The peralkaline rocks should be known as

    such, and differ from the metaluminous to weakly per- influx into a localized area.

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    KING et al. ALUMINOUS A-TYPE GRANITES

    Carmichael, I. S. E. & McKenzie, W. S., 1963. FeldsparliquidACKNOWLEDGEMENTSequilibria in pantellerites: an experimental study.American Journal of

    This manuscript benefited from constructive reviews by Science261, 382396.Champion, D. C., 1991. Felsic granites of far north Queensland.John Hogan, John Foden and an anonymous reviewer.

    Unpublished Ph.D. Thesis, Australian National University, Can-We appreciate Tony Ewarts careful editorial assistance. berra, A.C.T.We are grateful for helpful conversations and data fromChappell, B. W., 1991. Trace element analysis of rocks by X-ray

    Phillip Blevin, Ian Williams, David Champion, Dennisspectrometry. Advances in X-ray Analysis34, 263276.

    Pogson, and Anthony Budd. Discussions with Phillip Chappell, B. W., 1994. Lachlan and New England: fold belts ofCandela, the late Robert Hill, Cal Barnes and Doone contrasting magmatic and tectonic development. Journal and Pro-Wyborn were also useful. John Holloway and Lee Silver ceedings, Royal Society of New South Wales127, 4759.

    Chappell, B. W. & Hergt, J. M., 1989. The use of known Fe contentare thanked for providing facilities during the final stagesas a flux monitor in neutron activation analysis.Chemical Geology 78,of manuscript production. Nick Ware, Tony Phimphisane151157.

    and Geoff Denton are thanked for help with analyticalChappell, B. W. & White, A. J. R., 1974. Two contrasting granite

    work. Figure 1 was drafted by the Cartographic Servicestypes.Pacific Geology 8, 173174.

    Unit at AGSO. Financial support from the Australian Chappell, B. W. & White, A. J. R., 1992. I- and S-type granites in theResearch Council Grant A39232908 is acknowledged. Lachlan Fold Belt.Transactions of the Royal Society of Edinburgh: Earth

    Sciences83, 126.

    Chappell, B. W., Williams, I. S., White, A. J. R. & McCulloch, M. T.,1990. Granites of the Lachlan Fold Belt. ICOG 7 Field Guide

    Excursion A-2. Bureau of Mineral Resources, Geology & Geophysics Record

    1990/48.

    Chappell, B. W., English, P. M., King, P. L., White, A. J. R. & Wyborn,

    D., 1991. Granites and related rocks of the Lachlan Fold Belt (1:1 250 000

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