Wetar PDF

10.1007/s00126-005-0468-x http://proxy.bib.uottawa.ca:2344/media/9C5VVKTXY3K4K8XVN...
Mineralium Deposita
International Journal for Geology, Mineralogy and Geochemistry of Mineral Deposits
© Springer-Verlag 2005
10.1007/s00126-005-0468-x
Article
The development of volcanic hosted massive

sulfide and barite–gold orebodies on Wetar
Island, Indonesia
Philip M. Scotney1, 5 , Stephen Roberts1 , Richard J. Herrington2 , Adrian J. Boyce3 and
Ray Burgess4
(1) School of Ocean and Earth Science, Southampton Oceanography Centre, University of Southampton, Southampton,
SO14 3ZH, UK
(2) Department of Mineralogy, Natural History Museum, Cromwell Road, London, SW7 5BD, UK
(3) Isotope Geosciences Unit, SUERC, East Kilbride, Glasgow, G75 0QF, UK
(4) Department of Earth Sciences, University of Manchester, Manchester, M13 9PL, UK
(5) Present address: WRG, 3 Sidings Court, White Rose Way, Dancaster, DN4 5NU, UK
Philip M. Scotney
Email: philip.scotney@wrg.co.uk
Phone: +44-1234-353996
Received: 25 January 2005 Accepted: 7 February 2005 Published online: 12 April 2005
Abstract Wetar Island is composed of Neogene volcanic rocks and minor oceanic sediments and
forms part of the Inner Banda Arc. The island preserves precious metal-rich volcanogenic massive
sulfide and barite deposits, which produced approximately 17 metric tonnes of gold. The
polymetallic massive sulfides are dominantly pyrite (locally arsenian), with minor chalcopyrite
which are cut by late fractures infilled with covellite, chalcocite, tennantite–tetrahedrite, enargite,
bornite and Fe-poor sphalerite. Barite orebodies are developed on the flanks and locally overly the
massive sulfides. These orebodies comprise friable barite and minor sulfides, cemented by a series
of complex arsenates, oxides, hydroxides and sulfate, with gold present as <10 m free grains.
Linear and pipe-like structures comprising barite and iron-oxides beneath the barite deposits are
interpreted as feeder structures to the barite mineralization. Hydrothermal alteration around the
orebodies is zoned and dominated by illite–kaolinite–smectite assemblages; however, local alunite
and pyrophyllite are indicative of late acidic, oxidizing hydrothermal fluids proximal to
mineralization. Altered footwall volcanic rocks give an illite K–Ar age of 4.7±0.16 Ma and a
40Ar/39Ar age of 4.93±0.21 Ma. Fluid inclusion data suggest that hydrothermal fluid temperatures
were around 250–270°C, showed no evidence of boiling, with a mean salinity of 3.2 wt%
equivalent NaCl. The 34S composition of sulfides ranges between +3.3 and +11.7 and
suggests a significant contribution of sulfur from the underlying volcanic edifice. The 34S barite
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data vary between +22.4 and +31.0 , close to Miocene seawater sulfate. Whole rock 87Sr/86Sr
analyses of unaltered volcanic rocks (0.70748–0.71106) reflect contributions from subducted
continental material in their source region. The 87Sr/86Sr barite data (0.7076–0.7088) indicate a
dominant Miocene seawater component to the hydrothermal system. The mineral deposits formed
on the flanks of a volcanic edifice at depths of ~2 km. Spectacular sulfide mounds showing talus
textures are localized onto faults, which provided the main pathways for high-temperature
hydrothermal fluids and the development of associated stockworks. The orebodies were covered
and preserved by post-mineralization chert, gypsum, Globigerina-bearing limestone, lahars,
subaqueous debris flows and pyroclastics rocks.
Keywords Gold - Barite - Massive sulfide - Banda Arc - Submarine hydrothermal systems
Introduction
Spectacular examples of asymmetric massive sulfide mounds, flanked by barite deposits, are
preserved on Wetar Island, Indonesia. The orebodies occur marginal to hydrothermally altered
volcanic rocks, which overly ocean floor basalts, and are preserved beneath post-mineralization
Globigeriena-bearing limestones, lahars, subaqueous debris flows and pyroclastic rocks (Sewell
and Wheatley 1994; Herrington and First 1996; Scotney et al. 1999). Associated hydrothermal
alteration has argillic characteristics and the sulfide mounds contain pyrite, chalcopyrite, tennantite,
covellite and low-Fe sphalerite. Mineralization occurred at around 4.7 Ma (Herrington and First
1996) and, unusual for a volcanogenic massive sulfide (VMS) system, only the precious
metal-bearing barite resource was exploited. As a result, a subrecent VMS system is exceptionally
preserved and exposed within open pits and associated drill core. Ore at Kali Kuning contained
1.9 Mt at 4.6 g/t gold, 151 g/t silver and 60% barite, with 2.2 Mt at 4.0 g/t gold, 146 g/t silver and
40% barite at Lerokis (Abadi 1996).
Volcanogenic massive sulfide systems are often significant repositories of gold and silver (see
Hannington et al. 1999 for review). Various factors are recognized to play an important role in the
gold enrichment. These include the tectonic setting of the deposits, which in turn influences the
nature of the igneous basement, and the physical and chemical characteristics of the hydrothermal
fluids, in particular temperature, salinity and oxygen fugacity (Hannington et al. 1999). The gold
bearing characteristics of the sulfide assemblage and the argillic nature of the alteration at Wetar
Island, has led to speculation that the hydrothermal fluids responsible for the gold mineralization
contained a significant contribution of magmatic volatiles (Sillitoe et al. 1996). This paper describes
the mineralization and alteration preserved on Wetar, and the results of fluid inclusion and stable
and radiogenic isotope studies. These new data provide a better understanding of the nature and
origin of the hydrothermal mineralizing system. Furthermore, as a relatively young system of
Miocene age, the Wetar deposits provide an ideal opportunity to link observations from active
systems on the ocean floor with a system only recently incorporated into the geological record.
Geological setting
Wetar Island forms part of the Inner Banda Arc, an array of active and inactive volcanic islands
surrounding the Banda Sea, which are the result of the arc-continent collision of the NNE moving
(75 mma–1) Indian–Australian plate beneath the Eurasian plate (Audley-Charles 1986; Masson et
al. 1991) (Fig. 1). This zone of plate contact lies along the Java Trench to the west and continues
into the Timor Trough. Seismic refraction surveys indicate that the Timor–Tanimbar Trough
(1,200 km in length, up to 70 km wide and 2–3 km deep) is presently underlain by continental
lithosphere, varying between 31 km and 40 km in thickness from west to east (Audley-Charles
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1986; Masson et al. 1991).
Fig. 1 Location map of Wetar Island, Indonesia showing principal tectonic and volcanic features of
the Banda Arc. After Hamilton (1979), Varekamp et al. (1989), Breen and Silver (1989) and Masson
et al. (1991). The Banda Arc is divided into an Outer non-volcanic and Inner volcanic arc. The
extent of the Australian continental crust is shown within the inset
The Outer Banda Arc is dominantly non-volcanic in origin, with Timor, to the south of Wetar
preserving an accretionary prism and central collision complex, which was accreted onto the front
of the Australian continental plate. Richardson and Blundell (1996) proposed that a substantial part
of the collision complex consists of a micro-continental fragment that lay some considerable
distance to the north of the Australian continental margin, and which collided with the subduction
zone at approximately 8 Ma. Seismic velocity and gravity modelling suggests that the collision
complex across the Timor profile is 37–60 km thick and 135–160 km wide (Woodside et al. 1989;
Richardson and Blundell 1996). The frontal portion of this collision complex consists of a number
of high-angle thrusts imbricated from the subducting Australian continental margin (Hughes et al.
1996) (Fig. 2). Uplift rates in both the accretionary zone and associated islands of the inner
volcanic arc are high, with eastern parts of Timor presently situated 3 km above sea level (Snyder
et al. 1996). Microfaunal and palaeobathymetry studies, on the islands of Timor, Buru, Seram and
Kai, show that continent-arc collision has produced episodic uplift of the outer islands at rates of
between 500 mm ka–1 in a million years, to 5,000 mm ka–1 in some hundreds of thousands of
years (De Smet et al. 1989). These results indicate that uplift rates differ greatly along the arc, with
some islands experiencing long episodes of submergence intermittent with rapid pulses of uplift
during the Pliocene–Quaternary.
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Fig. 2 Simplified cross-section of the Banda Orogen based on geophysical data from Masson et al.
(1991), Richardson and Blundell (1996) and Snyder et al. (1996). Timor was formerly an outlier of
Australian continental crust and is now trapped between the Inner Banda Arc and the Australian
continental margin. The collision zone is dominated by shallow, southward dipping faults, which have
accommodated crustal shortening and thickening within the zone of collision
A complex zone of normal and strike-slip faulting offsets the Inner Banda Arc between the islands
of Alor and Wetar, to a distance of approximately 50 km (Fig. 1) (Masson et al. 1991). Recent
GPS measurements, seismicity data and seismic reflection profiles suggest that the Wetar Thrust,
located at the northern edge of the inactive segment of the Inner volcanic Banda Arc,
accommodates the majority of the present day 75 mma–1 convergence, between the Australian
margin and the Banda Arc (Silver et al. 1983; McCaffrey 1988; Genrich et al. 1994). This thrust
may represent the site of incipient arc reversal, due to the increased difficulty in subducting the
buoyant Australian continental plate post-arrival of the Australian continental margin with the
collision zone at approximately 2.4 Ma (Richardson and Blundell 1996).
Materials and methods

Geological information was obtained from the open-pit mines, outcrops and exploration drill-core.
Polished thin sections were examined in both reflected and transmitted light. Standard XRD and
FTIR methods were employed to characterize alteration mineralogical assemblages on 135 samples.
Mineral chemistry was determined by electron microprobe analysis using a Cameca SX50 at the
Natural History Museum, London. Operating conditions were 15 kV (accelerating voltage), 20 nA
(beam current) and count time of 20 s.
Doubly polished fluid inclusion chips were prepared to a thickness of 100 m. Microthermometric
analyses were completed on a Linkam TMS600 stage calibrated against a pure H2O–CO2 inclusion
at low temperatures, and checked daily against internal standards. Accuracy is estimated at ±0.1°C
for low-temperature phase changes (–100°C to 0°C) with a precision ±0.1°C and ±2°C, for
homogenization measurements between 100°C and 400°C, respectively.
Sulfides were prepared for conventional isotopic analysis at SUERC by standard heavy liquid,
magnetic, diamond micro-drilling and hand picking techniques. Barite was prepared by
micro-drilling. In both cases, around 5–10 mg was used for isotopic analysis. Minor contamination
by non-S-bearing phases was tolerated, and has no effect on the final data. Sulfides were analyzed
by standard techniques (Robinson and Kusakabe, 1975) in which SO2 gas was liberated by
combusting the sulfides with excess Cu2O at 1,075°C, in vacuo. Barite analyses were performed
by the technique of Coleman and Moore (1978), in which SO2 gas is liberated by combustion with
excess Cu2O and silica, at 1,125°C. Liberated gases were analyzed on a VG Isotech SIRA II mass
spectrometer, and standard corrections applied to raw 66SO2 values to produce true 34S. The
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standards employed were the international standards NBS-123 and IAEA-S-3, and the SUERC
standard CP-1. These gave 34S values of +17.1, –31 and –4.6 , respectively, with 1
reproducibility better than ±0.2 . Data are reported in 34S notation as per mil ( ) variations
from the Vienna Cañon Diablo Troilite (V-CDT) standard. Selected barite concentrates for sulfate
oxygen analyses were carefully cleaned by washing in Aqua Regia, and thorough rinsing in
deionized water. Oxygen was then extracted following the method of Hall et al. (1991). The
evolved CO2 was analyzed on a VG Sira 10 mass spectrometer, with all results reported in
standard delta notation as variations relative to the V-SMOW international standard. Replicate
analyses of the NBS-127 BaSO4 standard during these analyses gave +9.6±0.3 .
Sr isotopes were measured at Southampton Oceanography Center on a seven-collector VG Sector

54 mass spectrometer with a separable-filament source. Isotope ratios were determined as the
average of >100 ratios by measuring ion intensities in multidynamic collection mode and
fractionation corrected by normalization to 86Sr/88Sr = 0.1194. Measured values for standard NBS
SRM-987 were 87Sr/86Sr = 0.710242 ±13 (2 SD, n=42).
Stepped heating Ar/Ar data for biotite grains and illite separates (<2 m), were analyzed at the
University of Manchester, UK with analytical techniques following that of Kendrick et al. (2001).
Samples of the syeno-granite and dacite were disaggregated by light crushing, and individual
biotite grains (2–5 mm in length) were hand picked and cleaned in deionized water. Due to the
fine-grained nature of the illite sample it was expected that there would be significant recoil loss of
39Ar during irradiation, therefore, this sample was vacuum encapsulated in a quartz vial prior to
irradiation. The recoil 39Ar gas was extracted using an ultra-violet wavelength laser to drill into the
tube. The recoil 39Ar amounted to only 5% of the total 39Ar released from the sample and was
recombined in the total age calculation.
Geology of Wetar Island

Wetar Island measures approximately 110 km by 40 km and is composed entirely of Neogene
volcanic rocks and minor oceanic sediments (Sewell and Wheatley 1994). Submarine,
basaltic–andesites, with local pillows, form the volcanic basement to the island (Fig. 3). The
basaltic–andesites are intruded by rhyo-dacite domes (Ruxton 1989) and overlain by dacitic lavas,
tuffs and breccias, debris flows and lahar deposits (Fig. 4). Reef limestones are evident around the
perimeter of the island at varying heights.
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Fig. 3 Simplified geological map of Wetar Island, after Nash and Snodin (1992) and Farmer and
Clifford (1993). The map shows the principal mineralized areas, structural lineaments, and key
geological units
Fig. 4 Stratigraphic column and summary of tectonic and geochronological data from the Kali
Kuning, Lerokis and Meron areas of Wetar Island. Age constraints are: (1) Scotney 2002 (Ar/Ar); (2)
Herrington 1993 (K/Ar); (3) Abbott and Chamalaun 1981 (K/Ar); (4) Herrington 1993, a
biostratigraphic age for a post-mineralization Globigerina bearing limestone from the Kali Kuning
deposit. The Zanclian and Messinian aged strata are locally referred to as the mine sequence
Radiometric dating, largely K–Ar, of the volcanic assemblages suggests that the basement volcanic
rocks, to the south of the island, were extruded around 12 Ma with overlying dacites, diorites and
basaltic–andesites deposited between 7.78 Ma and 3.03 Ma (Abbott and Chamalaun 1981). A
Globigerina-bearing limestone outcrops on Wetar Island, which locally overlies basaltic–andesitic
volcanism and mineralization hosted by calc-alkaline andesites to rhyodacitic flows. This limestone
yields a biostratigraphic age of between 5.2 Ma and 3.9 Ma (Herrington 1993), and based on the
ratio of planktonic:benthic assemblages (Table 1), is likely to have formed in up to 2,000 m of
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water and possibly deeper (J. Murray, personal communication). Uplift rates for Wetar based on
these parameters are 420–570 mm ka–1, which are consistent with the lower rates calculated for
Timor in the outer arc (De Smet et al. 1989; Audley-Charles 1986b). Based on these uplift rates,
the localized areas of mineralization on the Wetar Island edifice would have emerged from the
Banda Sea between 0.5 Ma and 0.4 Ma. However, the central spine of Wetar (1,500 m, present
height) would have emerged around ~3 Ma based on the current height differentials, and likely
uplift rates.
Table 1 Planktonic and Benthic foraminifera assemblages identified within post-mineralization

limestones at Kali Kuning
Planktonic assemblage includes Benthic assemblage includes

Orbulia universa Cibicidoides
Globigerinoides conglobatus Globocassidulina
Globigerinoides sacculifer Favocassidulina
Globorotalia menardiform group Fontbotia
Sphaeroidinella dehiscens Pleurostomella
Stilostomella
Uvigerina
Planktonic:Benthic ratio = 99:1
Subaerial lahars generated along the central spine of Wetar developed into extensive subaqueous
debris flows. These units, locally up to 250 m in thickness, covered mineralized areas and infilled
topographic depressions. After collision of the Australian margin with the Outer Banda Arc, at
approximately 2.4 Ma (Richardson and Blundell 1996) uplift may have been substantially
increased. In particular, the development of the Wetar thrust and subsequent back-arc thrusting may
have aided in the rapid exhumation of the Wetar volcanic edifice.
Geology of the sulfide deposits
Volcanic and structural setting of the deposits
The economic deposits of Kali Kuning and Lerokis zones 4 and 5 are located towards the central
and northern part of the island (Fig. 3). These deposits, and the majority of other recognized
mineralized zones, which lie within the central part of the island, are bound to the west and east by
extensive NW–SE and NE–SW trending faults. The base of the volcanic stratigraphy comprises
fine-grained basaltic–andesitic flows, which dip around 10° towards 028°. Overlying the basal
vesicular basalts and basaltic–andesites is a >450 m thick sequence of altered volcanic rocks,
locally termed the mine sequence (Fig. 4). At the base of this sequence green, chloritic altered,
vesicular pillow lavas are well preserved. Up section andesitic to rhyodacite flow units and local
breccias are preserved, and these are the host rocks to the mineralization. Unconformably overlying
this sequence are a series of post-mineralization lahars and debris flows, which appear
geomorphologically controlled by the palaeotopography. Local hydrothermally altered dykes
cross-cut the mine sequence, with clear evidence of post-mineralization dykes restricted to
unaltered E–W striking andesitic dykes, which cut lahars and debris flows within coastal
exposures.
The deposits are discordant to the local stratigraphy and are associated with faults. The Lerokis
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zone 5 mound developed at the intersection of a northwest and westerly trending structure and the
Kali Kuning sulfide mound is located along a northwesterly trending fault.
Massive sulfides
Two well-preserved polymetallic sulfide mounds at Kali Kuning and Lerokis zone 5 have exposed
dimensions of ~15010070 m and ~1209030 m, respectively (Fig. 5a–d). Pre-mining, no
sulfide mounds were exposed at the surface. In plan, the mounds are broadly arcuate. The sulfide
mounds are blocky in appearance, with clasts of massive pyrite ranging in diameter from a few
centimeter up to boulders some 30 cm across (Fig. 6). Talus and redeposited sulfides occur
marginal to the mounds where matrix supported angular fragments of massive sulfide are held in a
fine-grained sulfide mud. Minor evidence for seafloor reworking is evident at Lerokis zone 5,
where a 30 cm zone of interbedded sulfide and volcaniclastic material overlies the mound. Chert,
gypsum and globigerina-bearing limestone overlie the Kali Kuning sulfide mound. At the margin
of the sulfide mounds, fine-grained poorly consolidated granular pyrite marks the contact zone
(0.2–2.5 m) between the sulfide mound and the associated barite deposits. The mineralogy of the
massive sulfide mounds is dominated by pyrite, accounting for >98% of all sulfides present with
minor amounts of chalcopyrite and sphalerite. Typical of seafloor sulfides, the pyrite and
chalcopyrite often show porous textures as well as collomorphic growth zones up to 3 mm
across (Fig. 7a). The collomorphic pyrite tends to nucleate on and around euhedral pyrite grains
(Fig. 7b). This texture appears most frequently at the margins and upper parts of the sulfide
mounds. Chalcopyrite frequently rims and locally replaces pyrite (Fig. 7c) and is more apparent at
the margins of the sulfide mounds and particularly at the base of mounds and in the underlying
footwall. Occasional banding of pyrite and chalcopyrite is evident on a centimeter scale. A later
fracture network permeates the pyritic mounds, with a sulfide assemblage dominated by covellite,
Fe-poor sphalerite and lesser amounts of tennantite and tetrahedrite and tabular barite laths
(Fig. 7d). Overall, typical sulfide abundance within the mounds are
pyrite >> chalcopyrite > sphalerite > covellite/marcasite/tennantite/tetrahedrite and bornite. No
sulfide mound is evident at the Lerokis zone 4 deposit despite drilling beneath the barite
mineralization. All three deposits are surrounded by extensive gossanous material.
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Fig. 5 a View north–northwest of the Kali Kuning (KK3) deposit. The irregular nature of the sulfide
mound is clear; pre-mining, the entire mound was covered by baritic ore. Hydrothermal alteration is
evident around the deposit, post-mineralization lahars / debris-flows are shown. b Exposed sulfide
mound at Kali Kuning. Height of the sulfide mound is approximately 60 m. c Lerokis zone 5 situated
at a topographic height of 550 m on a prominent ridge (view approximately north). The host
depression for the barite ore deposit is evident. Conformable, post-mineralization
volcaniclastic-sediment overlies the massive sulphide mound. Pre-mined and remediated zones 1, 2
and 3 are also shown. d Exposed sulfide mound at Lerokis zone 5, height of the sulfide mound
above the pit floor is approximately 15 m. Extensive gossanous material surrounds both deposits
Fig. 6 Blocky sulfide talus at the base of the Lerokis zone 5 sulfide mound
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Fig. 7 Photomicrographs of polished sulfide sections: py pyrite; cpy chalcopyrite; sp sphalerite; ba

barite; ten tennantite; cov covellite; si silica. a–e field of view = 5 mm, f field of view = 2.5 mm. a
Collomorphic pyrite (sample 097056, Lerokis zone 5) within the massive pyritic sulfide mound. b
Euhedral pyrite cores overgrown by collomorphic pyrite (sample 097009). c Chalcopyrite replacement
of pyrite (sample 097059). d Fracture-fill sulfide assemblage (sample 097016). e Disseminated pyrite
within an altered volcanic clast in the Lerokis zone 5 footwall, rimmed by pyrite and a fracture-fill
assemblage of sphalerite and covellite (sample 097122). f Detail of fracture-fill sulfide assemblages in
e, showing variation in tennantite composition
Stockwork zones
The pyritic mounds at Kali Kuning and Lerokis zone 5 are underlain by stockwork zones which
reach to a depth of >210 m below the Lerokis zone 5 deposit and >150 m below Kali Kuning. The
stockwork zone is hosted by hydrothermally altered, locally vesicular, silicified volcanic rocks.
Brecciated, angular volcanic footwall clasts are rimmed by sulfides up to 4 mm in thickness and
also contain disseminated sulfides (Fig. 7e). The stockwork veins range from <1 mm up to 4 cm in
width and contain pyrite, chalcopyrite and sphalerite. Intense vein and disseminated mineralization
occurs within an extremely silicified zone immediately beneath the sulfide mound at Lerokis zone 5
and appears to be related to a fault intersection. Disseminated pyrite is also abundant in this zone
and is generally euhedral to subhedral (usually <1 mm). Gold was observed in association with a
zone of intense clay (illite) alteration in the stockwork beneath the Lerokis zone 5 sulfide mound
(Herrington 1993). A late sphalerite, tennantite and covellite-rich fracture network (Fig. 7e, f)
locally permeates the stockwork zone.
Barite deposits
The mined gold-rich barite deposits have been termed barite sands by Sewell and Wheatley (1994)
and Scotney et al. (1999) due to their unconsolidated friable nature. At Kali Kuning and Lerokis
zones 4 and 5 the deposits contain on average ~60–70% barite, and up to 90% barite where more
massive. The barite consists of a friable mass of barite crystals, which shows variable degrees of
cementation and colour variation, such that chaotic bedding with evidence of slumping are locally
defined. Individual barite crystals typically range in size between 2 mm and 4 mm, up to a
maximum of approximately 7 mm in length. Barite crystals typically show euhedral, rectangular,
rhombohedral and polyhedral forms (Fig. 8a). Cross-bedding within the barite is reported by
Sewell and Wheatley (1994), suggesting the local reworking of barite on the seafloor; however,
these features were largely evident pre-mining and within the upper parts of the deposits. At Kali
Kuning, barite overlies and locally surrounds the sulfide mound. The contact zone between the
massive sulfide and barite deposit is gradational, with a zone of granular pyrite, clay and barite up
to 2 m thick.
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Fig. 8 a SEM image of rectangular, rhombohedral and polyhedral interlocking barite crystals from the
Kali Kuning ore zone (sample 096879). b Relationship of aresendescloizite (ad), arsenbrackebuscite
(ab) and mimetite (m) as cementing phases within the Lerokis zone 4 barite ore zone. c Secondary
nature of anglesite (an) pseudomorphing galena and cementing barite laths. d Barite lath rimmed by
jarosite (ja) and subsequently rimmed / cemented by karibibite (k) and arsenbrackebuscite (ab)
The matrix of the poorly consolidated barite largely comprises collomorphic Fe-oxide, traces of
clay material and arsenates (Table 2), with increased cementation towards the footwall contact.
Arsendescloizite, arsenbrackebuscite and mimetite are all found intergrown, cementing tabular
barite (Fig. 8b). Anglesite is observed pseudomorphing galena and as a cementing phase to tabular
laths of barite and brecciated fragments (Fig. 8c). Arsenbrackebuscite occurs as rhombic crystals
(<20 m) showing compositional zoning (Fig. 8b,d), with cores depleted in As and Pb and
enriched in Sb and S compared to the margins; this phase also occurs as amorphous cement.
Euhedral barite laths are cemented by jarosite and a complex intergrowth of karibibite and
arsenbrackebuscite (Fig. 8d). Gold occurs in the baritic ore unit as free grains and in one instance
attached to a barite lath (Fig. 9). An association between gold and Fe-oxides is also noted by
Herrington (1993). The Hg bearing phase moschellandsbergite occurs at the stratigraphically
highest position of the Kali Kuning barite ore zone near to the overlying chert and limestone cover,
whereas, the Ag-bearing mimetite phase along with the majority of the complex arsenates tend to
occur at the base of the Lerokis zone 4 barite deposit; which coincides with the highest Au and Ag
grades reported towards the base of other ore zones, e.g. Lerokis zone 1 and Kali Kuning (Sewell
and Wheatley 1994).
Table 2 Barite ore cementing and inclusion phases identified at Wetar Island
Minerals identified cementing barite Minerals identified included within barite

Anglesite: PbSO4 Sphalerite: ZnS
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Minerals identified cementing barite Minerals identified included within barite
Romerite: Fe2+ Fe23+ (SO4)4·14H2O Galena: PbS
Silica/Jasper: SiO2 Chalcopyrite: CuFeS2
Mimetite: Pb5(AsO4)3Cl Argentite: Ag2S

Moschellandsbergite: Ag2Hg3 Acanthite: Ag2S
Jarosite: KFe33+ (SO4)2(OH)6 Pyrite: FeS2
Fe-oxides Bournonite: PbCuSbS3

Arsendescloizite: PbZn(OH)(AsO4) Bornite: Cu5FeS4
Arsenbrackebuscite: Pb2(Fe,Zn)(AsO4)2·H2O Jordanite: Pb14(AsSb)6S23
Karibibite: Fe23+ As43+ O9 Boulangerite: Pb5Sb4S11
Plumbojarosite: PbFe63+ (SO4)4(OH)12 Geochronite: Pb14(SbAs)6S23
Perroudite: (Hg5Ag4S5Cl4) Stibio-Luzonite: Cu3SbS4
Clorargyrite: AgCl Enargite: Cu3AsS4

Cerussite: PbCO3
Dusserite: BaFe3(AsO4)2(OH)·5H20
Cinnabar: HgS
Copiapite: Fe2+ Fe3+ 4(SO4)6(OH)2·20H2O
Romerite: Fe2+ Fe3+ 2(SO4)4·14H2O
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Fig. 9 Anhedral, <20 m gold grains adhering to barite laths
Variable amounts of sulfide phases, predominantly pyrite and galena are included within the barite
laths (see Table 2). Included phases range from euhedral to anhedral in form and the size of
inclusions are generally <50 m in diameter. Significantly more sulfides are included within barite
laths from the barite orebodies compared to barite inclusions from within the sulfide mound and
stockwork structures.
Barite also occurs as disseminated laths within stockwork zones (up to 1 cm), as vug fill within
sulfide mounds, associated with the fracture-fill sulfide assemblage and as coatings on external
sulfide mound faces. Vein barite occurs both proximal and distal to mineralization with individual
crystals up to 5 cm in long dimension.
Iron oxide–barite pipe structures
Distinct iron oxide–barite structures are preserved at Kali Kuning and Lerokis zones 4 and 5.
These structures are pipe-like in appearance and, at Lerokis zone 4 (Fig. 10), are 1–1.5 m high and
~1.5 m in diameter and are located towards the base and central part of the mined barite deposit. At
Lerokis zone 5 two irregular structures (1 m 12 m) are present (Fig. 5d) and at Kali Kuning two
iron oxide–barite pipe features are observed, one at the base of the mined barite ore zone, the other
directly underlying the chert and limestone cover rocks. All these structures comprise abundant
anastomosing layers of barite separated by layers of iron oxides, (goethite and limonite). Locally,
incorporated clasts of vesicular and highly altered volcanic rocks are noted, which were probably
derived from the volcanic footwall.
Fig. 10 Examples of Fe-oxide barite pipe structures, approximately 1.5 m in height, preserved at the
base of the Lerokis zone 4 barite ore deposit
Mineral paragenesis
The mineralization on Wetar can be subdivided into paragenetic stages based on observations from
the three major components of the systems: stockwork zone, sulfide mounds and barite deposits
(Fig. 11).
13 of 36 4/25/05 1:47 PM
Fig. 11 Paragenetic sequence for the mineralization events at the Wetar Island ore deposits
Stage I Pyrite (+ chalcopyrite + sphalerite + marcasite). Forming the massive sulfide mounds, and
associated stockworks.
Stage Ia Barite as poorly consolidated barite ore deposits, typically with inclusions of mound
sulfides, flanking the massive sulfide mounds. Gold is evidently associated with barite
precipitation. Notably, sulfide inclusions in the proposed feeder structures to the barite deposits
only contain inclusions of sulfides typically reported for the massive sulfide event, e.g. pyrite,
sphalerite, chalcopyrite, with no evidence of sulfosalts as inclusions.
Stage II Multiple fracture events reactivate the stockwork zone and the sulfide mounds. These
veins show chalcopyrite/sphalerite intergrowth, Fe-poor sphalerite, Zn-poor tennantite, Zn-rich
tennantite ± tetrahedrite, covellite, bornite, digenite and barite. Tabular barite laths up to 7 mm long
are associated with this event.
Stage III Late barite veins with individual crystals up to 5 cm developed both proximal and distal
to mineralization and coating external faces of the sulfide mounds.
Stage IV Cementation of the barite deposit by oxides, arsenates and sulfates other than barite (see
Table 2) and partly through the local oxidation of sulfides. The relationship of this event to stage III
is uncertain.
Alteration
Intense zones of alteration are present within the footwall to Kali Kuning, and Lerokis zones 4 and
5. At the Kali Kuning orebody, the immediate footwall to the sulfide mound and barite
mineralization exhibits intense silicification, including microcrystalline silica and cristobalite, and a
clay alteration assemblage of illite, pyrophyllite, kaolinite and minor alunite. This alteration gives
way laterally and vertically to an illite–smectite assemblage, which passes outwards to zones of
chloritic alteration (Fig. 12a). At Lerokis zone 5, a similar zonation is observed, with the most
intense alteration associated with the stockwork that underlies the sulfide mound. Beneath the
massive sulfide mound is a ~25 m thick zone of silicification, microcrystalline silica, and extensive
argillic alteration, illite, pyrophyllite and kaolinite. Beneath this zone the predominant alteration is
chloritic. At Lerokis zone 4 (Fig. 12b), which lacks an exposed sulfide body, the immediate
footwall to the barite deposit is a zone of quartz–illite rich alteration and microcrystalline silica.
Residual silica and local jarosite veins are observed (Fig. 12c, d). This alteration passes outwards
into a zone of quartz–illite, illite–smectite and finally chloritic alteration. Intense silicification is
observed within the footwall adjacent to all the barite deposits. More peripheral footwall zones to
the barite deposits show predominantly chloritic alteration, which is well exposed in road cuts
away from the mineralization.
14 of 36 4/25/05 1:47 PM
Fig. 12 a Illite–smectite and chloritic alteration zonation around the Kali Kuning ore following removal
of the barite. b Zoned alteration sequence around the Lerokis zone 4 orebody, major phases are
shown determined by XRD, FTIR and initially by PIMA: qtz microcrystalline quartz; ill illite; ja jarosite;
goe goetite; chl chlorite; sm smectite; kao kaolinite; al alunite. The rivers S. Koreng, S. Kelapa Tiga
and the mine road are shown. Located at the centre of the ore zone are the Fe oxide/barite pipe
structures. c Sample of residual silica collected from the centre of the barite ore zone footwall at
Lerokis zone 4. d Jarosite veining at Lerokis zone 4
The alteration around the Wetar mineralization is thus extensive, intensive and zoned. The dominant
alteration assemblages comprise silicification proximal to mineralization, moving outwards and
downwards to illite–smectite and finally to distal chlorite. Although spatially restricted, the
presence of pyrophyllite, kaolinite and local alunite suggest that low pH fluids at moderate
temperatures have contributed to the alteration in the immediate footwall to the sulfide mounds and
the barite ore deposits (Reyes 1990).
Mineral identification
Pyrite
Pyrite is ubiquitous in all associations except barite ores and the associated pipe structures where
iron is generally present as oxides. Stage I pyrite, forms the bulk of the sulfide mound contains a
distinct arsenian pyrite. This pyrite often shows complex grains or collomorphic banded zones
(Fig. 13a, b) and may contain up to 6.7 wt% As (Table 3). The arsenian cores to complex grains
often contain idiomorphic inclusions of barite. Overgrowth pyrite is characteristic of the later part
15 of 36 4/25/05 1:47 PM
of stage I, immediately pre-dating or coincident with main stage chalcopyrite. This later pyrite
(stage Ia) is characteristically arsenic-poor.
Fig. 13 Back-scattered electron microphotographs of As zonation within massive pyrite samples from
the Lerokis zone 5 sulfide mound. Point locations correspond to the microprobe traverse, the graphs
illustrate the variation of As along each sample, a sample 097009; b sample 099903
Table 3 Representative analysis of Wetar Island mineral phases from the Kali Kuning and Lerokis
orebodies, Indonesia
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py py ten bor sph sph tet ten bour g a cpy arg jor py Mi
Stage I Ia Ia Ia Ia II II II Ia Ia Ia Ia Ia Ia IV
Cem
Sulfide phases Sulfide inclusion phases within barite
pha
S 48.01 52.60 31.23 30.46 32.61 32.29 25.16 26.56 19.36 13.74 34.32 12.00 17.94 51.64 Cl 2.0
Ag – 0.19 0.05 0.10 – – 0.01 – 0.06 0.26 – 80.34 – 0.02 SO2 0.6
As 6.71 0.19 15.91 – – 0.07 7.02 17.79 1.83 0.07 0.10 0.06 11.12 1.42 FeO 0.2
Ba – – – 0.46 0.12 – – – 0.16 0.79 0.87 2.63 0.42 0.67 ZnO 0.1
Cd – – 0.07 – – 0.48 – – – – – – – – As2O5 22
Cu 0.03 0.20 45.80 62.21 0.23 1.56 38.56 41.24 12.78 0.02 34.62 0.06 0.03 0.23 SeO2 0.0
Fe 44.37 46.48 0.04 7.15 6.12 0.10 2.20 0.11 0.05 – 29.07 1.26 – 44.86 Ag2O 0.7
Hg – – – 0.03 0.06 – – – – – 0.14 0.65 – – PbO 73
Pb – – – – – – – – 41.08 84.37 – – 69.48 – Sb2O3 0.0
Sb – – 3.95 – 0.03 0.19 19.87 3.10 22.57 1.31 0.12 – 0.64 0.04 BaO 0.0
Se 0.04 0.38 0.13 0.03 0.03 0.04 0.05 0.06 0.03 0.01 – 1.20 0.05 0.04 HgO 0.0
Zn 0.04 – 0.16 – 58.28 64.98 5.22 8.30 – 0.16 0.07 0.01 – 0.18 Bi2O3 0.1
Total Total
99.20 100.04 97.34 100.43 97.48 99.71 98.07 97.16 97.92 100.73 99.30 98.21 99.68 99.08 99
Wt% compound%
Sulfide phases (wt %): py pyrite; sph sphalerite; tet tetrahedrite; ten tennantite; bour bournonite; ga
galena; cpy chalcopyrite; arg argentite; jor jordanite; bor bornite
Cementing phases (compound %): mim mimetite; ars arsendescloizite
Chalcopyrite
Chalcopyrite is associated with the overgrowth pyrite and locally replaces the earlier stage I pyrite.
Compositional variation in the chalcopyrite is negligible with respect to paragenetic association.
Chalcopyrite often occurs intergrown with later stage II barite.
Sphalerite
Sphalerite is associated with the chalcopyrite and as a later phase with sulfosalts and late barite.
Earlier chalcopyrite-associated sphalerite is generally opaque to translucent in thin section,
reflecting an elevated iron content of up to 6 wt% Fe. Later sulfosalt-associated sphalerite (stage II)
is generally iron-poor, often less than 0.1 wt% Fe (Table 3)
Sulfosalts
Tennantite is a minor accessory of the chalcopyrite–sphalerite stage of mineralization and is more

abundant in stage II cross-cutting veins containing covellite, digenite, bornite and barite. In the
earlier stage (chalcopyrite + sphalerite, Fig. 7d), the tennantite is generally zinc-poor with between
0 wt% Zn and 1 wt% Zn, ~31 wt% S, ~17 wt% As and 0.1–3.9 wt% Sb. In the later association
(+covellite), both zinc-poor and zincian tennantite are found (Fig. 7f). Zn-rich tennantite contains
up to 8.3 wt% Zn, ~27 wt% S and ~19 wt% As and between 0.4 wt% and 6.5 wt% Sb. Zincian
tetrahedrite is often seen as inclusions in Fe-poor sphalerite. Bournonite and jordanite are common
17 of 36 4/25/05 1:47 PM
as tiny inclusions in larger barite laths.
Minor sulfides
Covellite and digenite are common in the stage II veins and bornite plus argentite are common
inclusion phases in barite laths. The covellite from stage II cross-cutting veins in the sulfide mound
and stockworks contain between 0.2 wt% and 1.3 wt% arsenic.
Barite
Barite appears as a ubiquitous phase throughout the main sulfide mound, sulfide talus breccias,
barite ores, stage II stockwork veins and stage III veins. The mineral chemistry of the barites is
variable with both Sr-poor and Sr-enriched types present in samples from the stockwork and the
ore.
Barite cementing phases
The phases cementing the barite ores are largely iron oxides, hydroxides, complex arsenates and
sulfate phases, many of which are amorphous. Distinct phases analyzed include mimetite,
arsenbrackebuscite, arsendescloizite, anglesite and moschellandsbergite. Mimetite contains
significant silver, along with the minor argentite as inclusions in barite, and was probably the
source for the silver recovered in the vat-leach processing of the barite ore. Along with cinnabar,
metacinnabarite, perroudite and tiemannite (De Roever 1991), moschellandsbergite is a major host
for mercury in the barite ore, the presence of which was discovered during early gold production at
Wetar and subsequently recovered during processing (Sewell and Wheatley 1994).
Fluid inclusion studies

A representative suite of barite samples, encompassing all stages of ore paragenesis, were analyzed
using microthermometric techniques. These included samples from the stockwork zone, barite ore,
late vein barite and iron oxide–barite feeder structures to the barite ore. The majority of analyzed
samples (7 of 11) were collected from the Lerokis zone 5 deposit. Optical examination indicates
that >95% of all barite hosted inclusions are associated with secondary and pseudo-secondary
inclusion trails (Fig. 14a), approximately 5% appear primary. The solitary bi-phase primary
inclusions are two phase (L + V) and range in size from 12 m to 25 m; these are described type
1A. Type 1B are also two-phase liquid plus small amounts of vapour inclusions (L + V), which
occur as pseudo-secondary and secondary trails. Recognition of a few mono-phase (L) inclusions
(by first and final ice-melt phase changes) are described as Type 2. Inclusions are concentrated
towards crystal margins particularly in stockwork associated samples (Fig. 14b).
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Fig. 14 a–b Photomicrographs of barite hosted fluid inclusions from Wetar Island. a
Pseudo-secondary and secondary trails in samples 097084, decrepitated inclusions are also evident
(d). b Abundant 2 phase inclusions in sample 097106, a pronounced reduction in number of
inclusions is evident toward the crystal core
Microthermometry results
For all Type 1 fluid inclusions, the degree of fill (F) ranges from 0.6 to 0.95, typically around
0.9–0.95, no daughter phases are observed and many inclusions show evidence of decrepitation or
leakage (Fig. 15a). Homogenization of inclusions (Th) is consistently L + V to L and occurs
between 144°C and 314°C with a mode of 238°C (n=206) (Table 4, Fig. 15b). First ice-melt
temperatures (Tfm) occur between –20°C and –24.4°C (n=35), with final ice melting (TMice)
between –0.9°C and –3.1°C (mode –1.6); corresponding to salinities of 1.6–5.1 wt% equivalent
NaCl (Bodnar, 1993) (Fig. 15c and d). This suggests that salinities span the salinity of seawater
(~3.2 wt% equivalent NaCl).
19 of 36 4/25/05 1:47 PM
Fig. 15 Fluid inclusion microthermometric data from Wetar Island barite samples
Table 4 Isotopic and microthermometric data obtained for the Wetar samples
Material 34S 18O T h (°C) T Fm (°C) T mice (°C) N

Sample 87S r /86S r ±2 SE
analyzed (CDT) (SMOW) Range A v n Range Av n Range Av n (w
111943 Barite 22.78 0.70764 7 196–262 235 1 6 –22.1–22.8 –22.5 4 –1.4–2.3 –1.9 1 5 2
100134 Barite 24
096877 Barite 24.23

096878 Barite 26.98
096879 Barite 23.65 10.9 0.70773 7 209–289 242 2 1 –21–22.5 –21.9 4 –1–1.9 –1.6 1 7 1
096889 Barite 22.39
100133 Barite 9.1
100103 Gypsum 12.8 13.3 0.70909 7
096890 Pyrite 11.55

096858 Pyrite 8.55
096879 Pyrite 8.44
111943 Pyrite 9.52
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Material 34S 18O T (°C) T Fm (°C) T mice (°C) N

Sample 87S r /86S r ±2 SE h
111943 Chalcopyrite 10.25
100134 Pyrite 11.69
096857 Pyrite 10.37
097228 Pyrite 10.78
111942 Pyrite 8.47
100144 Native sulfur 15.8
097333 Pyrite 9.89
111979 Barite 25.18 6.5 0.70827

111931 Barite 26.3 7.7 0.70774 8 189–267 228 1 7 – –21.1 1 –1.1–2.1 –1.6 6 1
096948 Barite 24.6 8.7/9.4 0.70801 8 197–309 240 2 0 – –23 1 –0.9–2.4 –1.6 1 6 1
099917 Barite 24.2 8.4 0.70829 7 183–237 220 1 5 –20.4–21.8 –21.1 3 –1.6–2.6 –2.2 1 2 2
099939 Barite 23.9 6.8 0.70836 8 199–269 233 1 8 – –2.6 1 –1.2–1.8 –1.6 1 7 2
099938 Barite 31 11.3 0.70786 8 144–212 194 1 5 –22–24.4 –22.7 1 1 –1.4–2.7 –2.2 2 2 2
099933 Barite 27.8 10.5 0.7088 8
099923 Barite 24.5 7.8 0.7083 8
097106 Barite 27.5 7.7 0.70807 8 217–302 255 2 4 –20–21.8 –20.7 5 –1.8–3.1 –2.1 1 7 2
097106 Pyrite 3.33
097104 Sphalerite 6.1
097098 Pyrite 6.7
111997 Pyrite 7.25
099902 Pyrite 6.92

099917 Pyrite 6.26
097219 Pyrite 8.4
097122 Barite 28.1 8.6 0.70836 186–314 269 2 0 –22.1–22.5 –22.4 4 –1.9–2.8 –2.2 1 6 3
097059 Barite 22.7 5.8 0.70809 8
097024 Barite 24.6 11.3 0.70873 210–288 245 1 8 – – – –1.6–2.4 –2.1 1 1 2
097023 Barite 24.43
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Material 34S 18O T (°C) T Fm (°C) T mice (°C) N

Sample 87S r /86S r ±2 SE h
097098 Barite 25.04 8.9 0.70836
097084 Barite 27.02 8.6 0.70854 8 187–286 230 2 2 – –21.4 1 –1–2.1 –1.8 1 4 1
097084 Pyrite 9.03
097084 Sphalerite 4.26
097122 Pyrite 8.02
097122 Cov-spha-ten 6.91
097041 Pyrite 6.56

097024 Pyrite 8.57
097059 Pyrite 8.01
097059 Chalcopyrite 7.44
097023 Pyrite 7.52
097009 Pyrite 7.4
096920 Whole-rock 0.70773 17
096921 Whole-rock 0.70773 18
096922 Whole-rock 0.70775 17
096884 Whole-rock 0.70834 21
096168 Whole-rock 0.71166 20
096167 Whole-rock 0.71107 12
111914 Whole-rock 0.70747 17
097106 Whole-rock 0.70772 7
100129 Whole-rock 0.70789 9
111935 Whole-rock 0.70819 23
111999 Whole-rock 0.70803 21

111994 Whole-rock 0.70781 7
096926 Whole-rock 0.70748 9
KK Kali Kuning; L4 Lerokis Zone 4; L5 Lerokis Zone 5; cov-spha-ten covellite, sphalerite, tennantite
composite sample
Although the petrographic data allows the inclusions to be subdivided into Type 1A, 1B and Type
22 of 36 4/25/05 1:47 PM
2 inclusions, they show similar Th and salinity ranges throughout the paragenesis, which suggest
no significant evolution of the hydrothermal fluid throughout the barite crystallization and that a
single-phase fluid was responsible for the precipitation of barite within the system. However, the
variable salinities above and below that of seawater suggest that super-critical phase separation may
have occurred deeper in the system (Delaney and Cosens 1982; Bischoff and Pitzer 1985). The
Globigerina-bearing limestone caps the mineralization at Kali Kuning and preserves fauna,
including Favocassidulina, and benthic:planktonic foraminifera ratios, which suggest deposition
occurred at least 2,000 m below sea-level and possibly considerably deeper (J. Murray, personal
communication). These results contradict those of Sewell and Wheatley (1994), who suggested that
the mineralization occurred in water depths of <600 m. Based on a minimum depth estimate of
2,250 m and a maximum estimate of 3,000 m, the confining pressure equates to a homogenization
temperature correction of +23°C and +40°C (Bodnar and Vityk 1994). If the maximum correction
is applied, the Wetar Island average trapping temperature will be 275°C. The fluid inclusion data
suggest that the hydrothermal fluids responsible for the barite deposition throughout the Wetar
hydrothermal systems were similar in salinity and temperature to those currently venting as white
smoker fluids on active vent sites at mid-ocean ridges (Rona et al. 1993).
Stable isotopes
34S
34S analyses of 56 samples, comprising 29 sulfides, 25 sulphates, 1 gypsum and 1 native sulfur
from the deposits of Kali Kuning, and Lerokis zones 4 and 5, significantly expand on earlier data
and ranges reported by de Ronde (1995). Sulfides were collected from all stages of mineral
paragenesis and sulfates were recovered from barite bodies, within the mound sulfides and from
stockwork zones (Table 4).
Sulfides
The 34S values of pyrite within the massive sulfides range from 6.2 to 11.7 , stockwork
sulfides range between 3.3 and 9.8 (Fig. 16 and Table 4). The poorly consolidated granular
pyrite from the margins of the mounds, show a similar range of 34S to the massive sulfides of
between 8.5 and 11.7 . No significant variations are observed for the different sulfide phases,
sphalerite, chalcopyrite and a mixture of sphalerite, tennantite and covellite. The similarity of the
sulfide data from both the underlying stockwork and sulfide mounds suggests a common source of
sulfur at each deposit. The mean value of 34S for this study is 8 , close to 34S values of +5
and +7 reported for Indonesian arc lavas by De Hoog et al. (2001). It is suggested that
arc-related lavas are enriched in 34S as a result of the significant incorporation of reduced
seawater sulfate during petrogenesis. In general, disseminated sulfide in the stockwork system has
a similar range of 34S to the mineralization (mound and vein stockwork, Table 4). This
consistency of 34S suggests a genetic correlation between the volcanic sulfide and mineralization.
Anomalously heavy 34S is a common occurrence in these settings (e.g. Arribas 1995).
23 of 36 4/25/05 1:47 PM
Fig. 16 Comparison of sulfur isotope data from the Kali Kuning, Lerokis zone 4 and 5 sulfide barite
deposits
Sulfates
The 34S of sulfates recovered from the Barite deposits of Wetar varies between 22.4 and 26.9
, with the heaviest 34S values, up to 31 , recorded from the stage III barite veins distal to the
ore deposits (Fig. 16). Ohmoto et al. (1983) reported similar 34S barite values from Kuroko
deposits, whereas, Goodfellow and Franklin (1993) report barite 34S values from the Bent Hill
system, which are considerably less than seawater, by as much as 10 . The Wetar sulfate data
reflect or are heavier than the predicted Miocene seawater sulfate value of 34S 22 (Claypool et
al. 1980). Ohmoto et al. (1983) suggested that mixtures of seawater sulfate and hydrothermal fluid
sulfate, with equilibrium 34S values of between 29 and 34 between 280°C and 200°C,
could account for the values observed in Kuroko systems. However, only limited mixing of
seawater and hydrothermal fluid would return the 34S sulfate values to seawater, as modern vent
fluids contain extremely low levels of dissolved sulfate (Scott 1997). Chiba et al. (1998) suggested
that increases in 34S observed for anhydrite in the TAG mound is due to the partial reduction of
seawater sulfate by ferrous iron in the hydrothermal fluid. Given that the formation of barite
requires the mixing of seawater and hydrothermal fluid a similar interpretation is favored. The
heaviest 34S sulfate values are reported from the distal stage III barite veins and suggest that
seawater and hydrothermal fluid mixtures are subject to closed system reduction, highlighted by the
peripheral vein at +31 (Table 4, sample 099938). Notably, coexisting pyrite and barite pairs
commonly give unrealistic isotope equilibrium temperatures (usually higher), which corroborates
our observations that the pyrite and barite is seldom co-precipitated.
Goodfellow and Franklin (1993) account for the relatively light 34S data at Bent Hill, by the
mixing of barium in vent fluids with sulfate formed by the oxidation of pre-existing sulfides, or
H2S from the hydrothermal fluid, either within chimney structures or in the underlying sulfide
24 of 36 4/25/05 1:47 PM
mound. There is no evidence for this at Wetar. However, the gypsum and native sulfur 34S
values, suggest oxidation of excess H2S in the hydrothermal fluid and local oxidation of sulfides
may be important in their formation.
18O
The sulfate oxygen data vary between 18O of 5.8 and 11.3 (Table 4), with a mode at 9 .
As the barite 18O data are shifted to values both higher and lower than the composition of
seawater, the sulfate oxygen data suggests isotopic exchange has occurred. Nevertheless, the 18O
mode of 9 coincides with the 18O value of seawater sulfate and suggests that the bulk of barite
precipitated in equilibrium with seawater.
The 34S and 18O stable isotope data suggest the predominant source of sulfur in the sulfides
was derived from the volcanic rocks in the basement, with the sulfur in the sulfate largely derived
from seawater and reaffirms the importance of hydrothermal fluid and seawater mixing in the
formation of VMS systems (Teagle et al. 1998a, 1998b; Roberts et al. 2003).
87Sr/86Sr
Whole-rock 87Sr/86Sr analyses were completed on variably altered host volcanic rocks, and barite
separates from the massive barite bodies, fractures within the sulfide mounds and iron oxide-barite
pipe structures. The barite data range between 87Sr/86Sr 0.7076 and 0.7088 with no systematic
variation according to setting (Fig. 17). The 87Sr/86Sr ratios of the barites are considered to reflect
mixtures between Miocene seawater (87Sr/86Sr 0.70849, Farrell et al. (1978)) and hydrothermal
fluid. However, the majority of the data plot close to the value of Miocene seawater suggesting a
significant contribution of seawater to the barite formation.
Fig. 17 Histogram summarizing the range in 87Sr/86Sr for Wetar Island sulfate and whole rock data.
Data from Herrington (1996) is included. s syeno-granite; d dacite
25 of 36 4/25/05 1:47 PM
Notably, one analysis shows a 87Sr/86Sr ratio of 0.70644 (Herrington 1996), from the stockwork
of an undeveloped mineral prospect, Batu Kapal (Fig. 3). This value suggests that locally the
hydothermal end member value may be less than 0.70644, and also indicates that less radiogenic
basement may be involved in the source of Sr to this hydrothermal fluid.
The whole-rock data of variably altered basement show 87Sr/86Sr values between 0.7074 and
0.7116. These values are typically more radiogenic than MORB, and are consistent with data
reported from surrounding islands (Whitford et al. 1977; Margaritz et al. 1978; Varekamp et al.
1989; Vroon et al. 1993, 2001). The more radiogenic values of 0.71165 and 0.71106, from dacitic
flows, suggest a significant contribution of continental crust and or sediment in the generation of
these post-mineralization magmas (Vroon et al. 2001; Elburg et al. 2002). Values of up to 0.72227
are reported by McCulloch et al. (1982), however, the nature of these samples is uncertain.
The unaltered volcanic samples tend to show 87Sr/86Sr ratios between 0.70748 and 0.70781 and Sr
values >160 ppm (160–388); which are substantially changed during alteration. The progressively
altered samples show a significant decrease in whole-rock Sr concentration to <60 ppm with a
concomitant increase in the 87Sr/86Sr value from 0.70746 to 0.70833. The most highly altered
samples show Sr concentrations and 87Sr/86Sr signatures that suggest that the samples have
undergone complete isotopic exchange with seawater (Fig. 18).
Fig. 18 87Sr/86Sr v ppm Sr from variably altered Wetar volcanic rocks. Increased alteration coincides
with lower ppm Sr and more radiogenic 87Sr/86Sr ratios, reflecting increased interaction with Miocene
seawater. The syeno-granite and post-mineralization dacites are omitted from this figure
Ar–Ar age determinations

Three samples were chosen for Ar–Ar age determination in order to better constrain the age of
mineralization and volcanic events of the area. Samples of the following intrusive and volcanic
rocks were analyzed: (1) a syeno–grantite intrusion (sample no. 111999) collected from the Kali
Lurang river in the Meron area; (2) a post-mineralization capping dacite flow (sample no. 097167)
from Meron; and (3) a fine-grained illite (sample no. 056896, <2 m size fraction) collected from
the hydrothermally altered footwall volcanic rocks at Lerokis at a depth of 26 m below the
mineralization. Herrington (1993) reported a K/Ar age of 4.7±0.16 Ma for the illite sample.
Ar–Ar data are given in Table 5 and shown as apparent age spectrum diagrams in Fig. 19. Errors
26 of 36 4/25/05 1:47 PM
are quoted at the one standard deviation level and include the uncertainty in monitor age (Hb3gr
1072±11 Ma). An isotope correlation diagram of 39Ar/40Ar versus 36Ar/40Ar (not shown) reveals
that the trapped 40Ar/36Ar ratios are lower than the present day atmospheric ratio (295.5)
constrained most precisely by the syeno–granite sample to be 284±3. Previously, Nagy et al.
(1999) determined similar anomalously low 40Ar/36Ar ratios from dacite flows and attributed them
to either a minor contaminant at m/z 36 in the mass spectrometer, or fractionated atmospheric argon
within the samples. The age obtained from the illite sample of 4.93±0.21 Ma is within error of the
K/Ar age of the same sample (4.7±0.16 Ma) reported by Herrington (1993). The age of the
syeno–granite intrusion and dacite flow are 4.73±0.16 Ma and 2.39±0.14 Ma, respectively
(Fig. 19).
Table 5 Stepped heating Ar/Ar data for biotite grains and illite separates (<2 m), Wetar Island,
Indonesia. Amounts of Cl and K obtained from measured 38ArCl and 39ArK using the Hb3 gr monitor
and the parameters of = 0.542±0.01, = 4.37±0.03 and J = 0.017093±0.000026
Sample No. L o c a t i o n Sample type Weight (mg) Cl (ppm) K (Wt%) 40A r * 1 0–6 cc/g Age (Ma)
111999 Meron area Biotite 12 2,288±6 7.35±0.01 1.35±0.4 4.73±0.16
097167 Meron Biotite 11 9,404±7.1 8.73±0.01 0.75±1.2 2.39±0.14
056896 Lerokis Illite 9.1 13.88±0.90 7.90±0.01 1.38±0.05 4.93±0.21
Fig. 19 Age versus cumulative 39Ar released during stepped heating for the Wetar Island samples
27 of 36 4/25/05 1:47 PM
The age data indicates that the spatially related syeno–granite intrusion (proximal to the Meron
prospect) and the mineralization are the same age and therefore implies that this intrusive event
supplied heat to the hydrothermal system. The Ar–Ar age of the illite is within error of the
previously published conventional K–Ar age (Herrington 1993) and indicates mineralization of the
Lerokis deposit occurred between 4.7 Ma and 4.9 Ma. The age of the post-mineralization dacite
flow indicates that volcanism continued at least as recently as 2.4 Ma, which is the proposed age
for the collision and accretion of the Australian continental margin with the Outer Banda Arc in the
region of Timor (Richardson and Blundell 1996). The sample may record a period of extension
within the Inner Banda Arc as a direct result of compressional tectonics to the south in the Outer
Arc. The age of the dacite flow also indicates that the debris flow that overlies the Meron deposit
also occurred post-2.4 Ma. This new age data coupled with the Sr data confirms an increasingly
contaminated source region under Wetar Island, progressively modified by subducted continental
material (SCM) related to tectonic events further to the south.
Evolution of the hydrothermal system

The data collected suggest that the Wetar massive sulfide and barite deposits were formed on the
flanks of a volcanic edifice during the development of the Inner Banda Arc. Observations of the
volcanic stratigraphy and tectonics suggest the Wetar edifice initially formed around 12 Ma due to
extensive rifting and associated volcanism within oceanic crust. The mineralization is associated
with bimodal volcanism, on a basement of basalts and basaltic–andesite, which most likely formed
around 5 Ma, given the dates of the overlying mine sequence. The major sulfide mounds show
talus textures and are localized on faults, which provide the main pathway for high temperature
hydrothermal fluids and the development of associated stockworks (Fig. 20a). Within the massive
sulfide mound much of the pyrite is arsenian (up to 6.7 wt%), and given the established
relationship between arsenic and gold content of pyrite (Cook and Chryssoulis 1990; Cline 2001;
Pals et al. 2003) may represent an initial reservoir for Au subsequently remobilized by later
hydrothermal fluids responsible for the barite–gold ore. The pyrite 34S data suggest that the sulfur
is sourced from basement arc volcanic rocks, modified by a subduction zone component, which is
also suggested by the whole rock 87Sr/86Sr data. The slightly elevated 34S values, compared to
arc values, indicates a component of reduced seawater sulfate during pyrite precipitation. The
hydrothermal fluids responsible for sulfide precipitation produce a well zoned, intensive alteration
sequence (Fig. 12b) with illite–smectite centered on the mineralization and chlorite alteration deeper
and distal to the ore zones. The heat source driving the hydrothermal convection is most likely
intrusive syeno–granite bodies at depth, which from Ar/Ar dating are known to be coeval with
mineralization.
28 of 36 4/25/05 1:47 PM
Fig. 20 Schematic evolution of the Wetar deposits: a T1, the Wetar deposits initiated as typical
volcanogenic massive sulfides with a zoned footwall alteration predominantly propylitic to argillic in
character (Kuroko like). b T2, the barite deposits originate as a peripheral vent system, with fluids
circulating through the sulfide mound and undergoing significant mixing of seawater. As the system
evolves conductively cooled hydrothermal fluids circulate beneath the massive sulfide mound
generating the alteration and reflecting the passage of more oxidized and acidic fluids. This results in
the argillic to advanced argillic alteration observed. This is also the major Au-precipitation phase. c
T3, the sulfide and barite system is preserved beneath limestones and lahars, prior to exhumation
from the ocean floor, due to continued collision of the Australian continental margin and the Outer
Banda Arc
Following massive sulfide development, barium rich fluids are discharged as white smokers, from
the hydrothermal system and in particular at the margins of the sulfide mound (Fig. 20b). The
distribution of barite suggests these fluids exploit many of the fracture systems previously
employed to develop the massive sulfide mound. For example, barite infiltrates the base of the
sulfide mound and fills any voids and fractures present. The 34S barite data suggest that the
sulfate in the barite is predominantly seawater derived, whereas, the barium is most likely derived
from the destruction of feldspars, within the andesites and felsic volcanic rocks of the basement.
Fluid inclusion data show that the hydrothermal fluids were at around 250–270°C, with no
evidence of boiling. However, the salinities are greater and less than seawater, suggesting
super-critical phase separation may have taken place, prior to egress on the seafloor. The form,
location, isotope and fluid inclusion data of the iron oxide–barite structures, strongly suggest they
are the palaeofluid conduits for the barite deposits. Gold is significantly enriched in the barite
mineralization and is closely related to its formation and the most intense phases of alteration. The
presence of high levels of arsenic in the barite ore matrix suggest that zone refining of the initial
arsenian pyrite may be important. It is questionable whether black smoker mineralization was still
occurring at this time.
29 of 36 4/25/05 1:47 PM
The limited nature of the covellite dominated assemblage, and accompanying 34S, 18O data,
suggest that no significant contribution of magmatic volatiles was involved in the formation of the
Wetar orebodies. For example, no isotopically light 34S values were observed for sulfides or
sulfates compared to Hine Hina or Conical Sea-Mount (Herzig et al. 1998) at least no contribution
that could be detected beyond the copious amounts of seawater that must have circulated in the
system. There is no compelling evidence that the fluids responsible for mineralization boiled at the
sites of deposition, however, they may have been subject to supercritical phase separation, which is
becoming an increasingly recognized phenomenon in modern vent systems.
The sulfide and barite orebodies are preserved on the seafloor by the subsequent precipitation of
chert, gypsum and limestone and, perhaps most significantly, by the accumulation of lahars and
debris flows (Fig. 20c). A dacite flow, within the lahars and debris flows gives an age of 2.4 Ma
and records continued volcanism on the Wetar edifice post-3 Ma.
Discussion and comparisons

Wetar deposits in comparison with modern systems
The fluids responsible for barite precipitation with associated gold and sulfosalt assemblages show
strong similarities to late stage hydrothermal fluids reported elsewhere in modern seafloor deposits.
For example, late stage hydrothermal fluids rich in Pb, As, Sb, Ag, +Au were reported from Axial
Seamount (Hannington and Scott 1988); with up to 6.7 ppm Au reported from an associated
sulfosalt assemblage. Furthermore, galena, anglesite and sulfosalts of Pb, Ag, As, and Sb are
frequently associated with low-T venting fluids, and the mineralogy of white smokers are typically
enriched in barite, sphalerite and consistently report elevated Au values (Koski et al. 1984).
The Spire at Axial Seamount shows both high- and low-Fe sphalerite, with the higher values
associated with the main stage ore formation (Hannington and Scott 1988). This is also the case for
Wetar with low-Fe sphalerite restricted to the later fracture network. These data are consistent with
a fluid evolution that evolved from a reducing fluid at low pH and high T (350°C) to a relatively
oxidizing fluid at high pH and lower T due to cooling and mixing with seawater.
Gold is commonly associated with low-T fluids in modern hydrothermal systems. High
concentrations of gold are reported in low-T Zn–Ba–SiO2 precipitates (Hannington et al. 1986;
Hannington and Scott 1988; 1989). In the Zn-rich chimneys of Snake Pit, Cd, Pb, Sb, Ag and Au
are considered to have directly precipitated in the Zn-sulfides, with the highest Au contents
(>500 ppb) observed in the Zn-rich chimneys and massive Zn-rich sulfides at the surface of the
deposit (Foquet et al. 1993). At the JADE hydrothermal field, Au enrichment correlates well with
the barite content of the samples, with minute rounded Au grains observed between barite crystals
(Halbach et al. 1989, 1993). The Au-rich samples also showed higher concentrations of As, Ba,
Sb, SiO2 and Ag, similar to Wetar. The similarity between the Wetar gold mineralization and
observations from active white smoker systems is striking, suggesting there was a significant role
for such fluids in the origin of the mineralization.
Au-rich volcanogenic massive sulfides and Wetar

The mineralogy of the ore deposits at Wetar is highly analogous to that reported from back-arc
spreading centers, e.g, Lau Basin, where visible gold was first documented in a white smoker
chimney (Herzig et al.1993). In particular, the mineralogy and precious metal content of the Wetar
deposits are strongly comparable to hydrothermal vent fields developed on island-arc or continental
30 of 36 4/25/05 1:47 PM
crust, e.g. Okinawa Trough (Halbach et al. 1989, 1993). The importance of the Au-composition of
the igneous basement in the generation of Au-rich VMS is debated. Herzig and Hannington (1993)
suggest that back-arc lavas are not significantly enriched in gold compared to MORB, and that a
gold-enriched source is not a prerequisite to the development of gold-rich VMS systems.
However, Moss et al. (2001) investigating the Manus Basin, suggest that the Au-enriched arc
lavas, typically at 6 ppb compared to 1 ppb and below for MORB, may have an important
influence on the Au-forming potential of the system. Although not developed directly on
continental crust, the isotopic data for Wetar provide strong evidence for a significant component of
continental crust and or sediments in the generation of the volcanic edifice that hosts the VMS
mineralization. Using simple mass balance equations, the amount of basement required to be
stripped of gold to produce the Kali Kuning deposit significantly increases from 0.5 km3 for a
basement of 6 ppb Au to ~3 km3 for a basement with only 1 ppb Au. These values climb to 0.8
and 5 km3, if extraction efficiency rates more in keeping with experimental work are assigned
(Moss et al. 2001). Such a dramatic reduction in the rock volumes required to generate the
Au-mineralization suggests that the Au content of the volcanic basement may well play an
important role in the generation of Au-rich VMS. Herzig and Hannington (1993) note that gold
appears most abundant in sulfides associated with immature seafloor rifts in continental or
island-arc crust, settings dominated by calc-alkaline volcanic rocks, including andesites, dacites and
rhyolites. Notably, the Au-rich VMS system at Boliden is thought to have developed within
calc-alkaline to dacite rocks within an island-arc located on continental crust or a thin continental
margin (Vivallo and Claesson 1987; Allen et al. 1996; Billstrom and Weihed 1996). Similarly, the
Au-rich Eskay Creek deposit formed within a mid-Jurassic arc of calc-alkaline to dacitic rocks that
developed on an earlier Triassic arc and Palaeozoic volcanic and sedimentary rocks (Macdonald et
al. 1996).
Summary and conclusions

The massive sulfide and barite–gold mineralization of Wetar Island, Indonesia, provides a
significant perspective on the formation of Au-rich barite in arc situations. The mineralization at
Wetar relates to arc volcanism triggered as the Banda Arc and Australian continental plate collide.
Progressive stages of mineralization are recognized, dominated by the early arsenian pyrite with
associated chalcopyrite and minor barite. Later sulfosalts, low-Fe sphalerite and further stages of
barite and then oxide mineralization developed, leaving a complex mineralization over intensely
altered footwall volcanic rocks showing argillic and local advanced argillic alteration close to
mineralization. The presence of oxide-cemented barite ores and iron oxide-cemented barite pipes
are evidence of the later, oxidized hydrothermal fluid dominated by seawater sulfate. These
oxidized fluids released arsenic and gold from earlier arsenian pyrite precipitating free gold with
barite and complex iron-bearing arsenates with significant contained silver and mercury.
Acknowledgements PS acknowledges the generous financial support of BHP-Billiton, The

Natural History Museum and The University of Southampton. The logistical and financial support
of BHP-Billiton through Chris Farmer, David Hopgood, David First and James Macdonald is
particularly acknowledged. Tony Fallick, John Murray, Andy Barker, Robin Armstrong, Ernie
Rutter and Damon Teagle provided key insights throughout the project. The SUERC is funded
through support of the Natural Environment Research Council (NERC) and the Scottish
Universities. AJB is funded by NERC support of the Isotope Community Support Facility at
SUERC. We acknowledge careful review of the manuscript by Donna Sewell and an anonymous
referee.
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10.1007/s00126-005-0468-x http://proxy.bib.uottawa.ca:2344/media/9C5VVKTXY3K4K8XVN...

The development of volcanic hosted massive

1986; Masson et al. 1991).

Materials and methods

Sr isotopes were measured at Southampton Oceanography Center on a seven-collector VG Sector

Geology of Wetar Island

Table 1 Planktonic and Benthic foraminifera assemblages identified within post-mineralization

Planktonic assemblage includes Benthic assemblage includes

Planktonic:Benthic ratio = 99:1

Geology of the sulfide deposits

Volcanic and structural setting of the deposits

Fig. 7 Photomicrographs of polished sulfide sections: py pyrite; cpy chalcopyrite; sp sphalerite; ba

Minerals identified cementing barite Minerals identified included within barite

Minerals identified cementing barite Minerals identified included within barite

Romerite: Fe2+ Fe23+ (SO4)4·14H2O Galena: PbS

Silica/Jasper: SiO2 Chalcopyrite: CuFeS2

Mimetite: Pb5(AsO4)3Cl Argentite: Ag2S

Jarosite: KFe33+ (SO4)2(OH)6 Pyrite: FeS2

Fe-oxides Bournonite: PbCuSbS3

Arsenbrackebuscite: Pb2(Fe,Zn)(AsO4)2·H2O Jordanite: Pb14(AsSb)6S23

Karibibite: Fe23+ As43+ O9 Boulangerite: Pb5Sb4S11

Plumbojarosite: PbFe63+ (SO4)4(OH)12 Geochronite: Pb14(SbAs)6S23

Perroudite: (Hg5Ag4S5Cl4) Stibio-Luzonite: Cu3SbS4

Clorargyrite: AgCl Enargite: Cu3AsS4

Fig. 9 Anhedral, <20 m gold grains adhering to barite laths

Iron oxide–barite pipe structures

Tennantite is a minor accessory of the chalcopyrite–sphalerite stage of mineralization and is more

as tiny inclusions in larger barite laths.

Barite cementing phases

Fluid inclusion studies

Material 34S 18O T h (°C) T Fm (°C) T mice (°C) N

096877 Barite 24.23

100103 Gypsum 12.8 13.3 0.70909 7

096890 Pyrite 11.55

Material 34S 18O T (°C) T Fm (°C) T mice (°C) N

100144 Native sulfur 15.8

097333 Pyrite 9.89

111979 Barite 25.18 6.5 0.70827

099933 Barite 27.8 10.5 0.7088 8

099923 Barite 24.5 7.8 0.7083 8

097106 Pyrite 3.33

097104 Sphalerite 6.1

097098 Pyrite 6.7

111997 Pyrite 7.25

099902 Pyrite 6.92

097219 Pyrite 8.4

097059 Barite 22.7 5.8 0.70809 8

097024 Barite 24.6 11.3 0.70873 210–288 245 1 8 – – – –1.6–2.4 –2.1 1 1 2

097023 Barite 24.43

Material 34S 18O T (°C) T Fm (°C) T mice (°C) N

097098 Barite 25.04 8.9 0.70836

097084 Pyrite 9.03

097084 Sphalerite 4.26

097122 Pyrite 8.02

097122 Cov-spha-ten 6.91

097041 Pyrite 6.56

096920 Whole-rock 0.70773 17

096921 Whole-rock 0.70773 18

096922 Whole-rock 0.70775 17

096884 Whole-rock 0.70834 21

096168 Whole-rock 0.71166 20

096167 Whole-rock 0.71107 12

111914 Whole-rock 0.70747 17