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0361-0128/01/3318/109-15 $6.00 109
IntroductionOROGENIC or mesothermal lode gold mineralization in theform of gold-bearing quartz vein systems is present in manyaccretionary orogenic belts. Phanerozoic examples of thesevein systems occur in terranes of the Paleozoic-Triassic Tas-man orogen of southeastern Australia, the Jurassic-early Ter-tiary North American Cordilleran orogen from the MotherLode in California, through the gold camps in British Colum-bia, to Nome, Alaska, and the middle to late Tertiary MonteRosa region of the Alpine orogen (Kerrich and Wyman, 1990;Goldfarb et al., 1997; Pettke and Diamond, 1997; Böhlke,1999). The chemistry of the ore-forming fluids, ore mineral-ogy, metal associations, P-T-XCO2 conditions of alteration andmineralization, and the late orogenic timing of these depositsare remarkably similar through time and space from theMesoarchean to the Cenozoic (Goldfarb et al., 1997; Groveset al., 1998; McCuaig and Kerrich, 1998; Kerrich et al., 2000;Ridley and Diamond, 2000; Goldfarb et al., 2001). However,
the ultimate source of the ore-forming fluids remains contro-versial. Proposed fluid sources include (1) granitoid-relatedorthomagmatic solutions (Burrows et al., 1986; Burrows andSpooner, 1987), (2) convecting meteoric water (Nesbitt et al.,1986, 1989), (3) mantle-derived fluids (Colvine et al., 1984;Fyon et al., 1984), and (4) fluids generated by deep de-volatilization of ocean crust and sediments in subduction-ac-cretion complexes (Kerrich and Wyman, 1990; Goldfarb etal., 1991a). The different models vary in terms of their impli-cations for crustal or mantle source reservoirs for the hy-drothermal ore fluids and solutes.
Nitrogen is one potential tracer for determining the sourceof the ore fluids. Ammonium ion (NH+
4) is the most commonform of nitrogen found in rocks, substituting for K+ in potas-sium-bearing silicates (Honma and Itihara, 1981; Bos et al.,1988; Guidotti and Sassi, 1998), and N2 has been recorded influid inclusions in some quartz veins (Bottrell et al., 1988; Or-tega et al., 1991). The isotopic composition of nitrogen haslarge variations in different geologic reservoirs, which makesthe nitrogen isotope system a potentially important tracer for
Metamorphic Origin of Ore-Forming Fluids for Orogenic Gold-Bearing Quartz Vein Systems in the North American Cordillera:
Constraints from a Reconnaissance Study of δ15N, δD, and δ18O
YIEFEI JIA,†
Department of Geological Sciences, University of Saskatchewan, 114 Science Place, Saskatoon, Saskatchewan, Canada S7N 5E2, and Re-search School of Earth Sciences, Australian National University, Canberra ACT 0200, Australia
ROBERT KERRICH,Department of Geological Sciences, University of Saskatchewan, 114 Science Place, Saskatoon, Saskatchewan, Canada S7N 5E2
AND RICHARD GOLDFARB
U.S. Geological Survey, Mineral Resources Program, Denver Federal Central, Box 25046, Mail Stop 964, Denver, Colorado 80225
AbstractThe western North American Cordillera hosts a large number of gold-bearing quartz vein systems from the
Mother Lode of southern California, through counterparts in British Columbia and southeastern Alaska, to theKlondike district in central Yukon. These vein systems are structurally controlled by major fault zones, whichare often reactivated terrane-bounding sutures that formed in orogens built during accretion and subductionof terranes along the continental margin of North America. Mineralization ages span mid-Jurassic to early Ter-tiary and encompass much of the evolution of the Cordilleran orogen.
Nitrogen contents and δ15N values of hydrothermal micas from veins are between 130 and 3,500 ppm and1.7 to 5.5 per mil, respectively. These values are consistent with fluids derived from metamorphic dehydrationreactions within the Phanerozoic accretion-subduction complexes, which have δ15N values of 1 to 6 per mil.The δ18O values of gold-bearing vein quartz from different locations in the Cordillera are between 14.6 and22.2 per mil but are uniform for individual vein systems. The δD values of hydrothermal micas are between–110 and –60 per mil. Ore fluids have calculated δ18O values of 8 to 16 per mil and δD values of –65 to –10per mil at an estimated temperature of 300°C; δD values of ore fluids do not show any latitudinal control.These results indicate a deep crustal source for the ore-forming fluids, most likely of metamorphic origin. LowδDH2O values of –120 to –130 per mil for a hydrous muscovite from the Sheba vein in the Klondike district re-flect secondary exchange between recrystallizing mica and meteoric waters.
Collectively, the N, H, and O isotope compositions of ore-related hydrothermal minerals indicate that theformation of these gold-bearing veins involved dilute, aqueous carbonic, and nitrogen-bearing fluids that weregenerated from metamorphic dehydration reactions at deep crustal levels. These data are not consistent witheither mantle-derived fluids or granitoid-related magmatic fluids, nor do they support a model involving deeplycirculated meteoric water.
Economic GeologyVol. 98, 2003, pp. 109–123
† Corresponding author: E-mail, [email protected]
the origin of terrestrial silicates and volatiles (Clayton, 1981;Javoy, 1997). Hydrothermal potassium-bearing silicates areubiquitous in alteration domains that develop within and/oradjacent to gold-bearing quartz veins. In greenschist faciesterranes muscovite, or Cr muscovite, is the most abundanthydrothermal potassium-bearing silicate, whereas in amphi-bolite facies-hosted deposits biotite is the dominant potas-sium-bearing silicate in the alteration assemblage. Both thedeposits and the alteration minerals formed broadly contem-poraneously with metamorphism of the host terrane (Mc-Cuaig and Kerrich, 1998). Therefore, hydrothermal micas inorogenic lode gold deposits are ideal for analyzing the nitro-gen contents and nitrogen isotope compositions, to constrainthe δ15N of the ore-forming fluid, and in turn the nitrogenisotope composition of the source reservoirs. Reconnaissancestudies on hydrothermal micas from Archean and Paleozoicorogenic lode gold deposits have proven the feasibility ofusing nitrogen isotopes to trace the origin of the ore-formingfluids for orogenic lode gold deposits (Jia and Kerrich, 1999,2000; Jia et al., 2001).
In this study, we present 100 analyses of nitrogen concen-trations and nitrogen isotope data for hydrothermal mus-covites separated from gold-bearing quartz-carbonate veinsfrom the western North American Cordillera. Included arethe Mother Lode of southern California, the Greenwood,Bridge River, Stuart Lake, Cassiar, and Atlin camps in BritishColumbia (BC), the Klondike district, Yukon Territory, andthe Fairbanks and Willow Creek districts of Alaska (Table 1).This new nitrogen isotope database of hydrothermal micas inorogenic lode gold deposits of the western North AmericanCordillera provides new constraints on the origin of the ore-forming fluids.
Hydrogen isotopes have traditionally been used by manyworkers to identify the source of ore fluids (see Taylor, 1997,for a review). The meteoric water model for orogenic gold de-posits was based on an apparent covariation of the δD of bulkdecrepitated fluid inclusions from gold-bearing quartz veinswith the latitudinally controlled variation of present and Ter-tiary meteoric water (Nesbitt et al., 1986; Zhang et al., 1989).Although there is an abundance of oxygen isotope data, onlylimited hydrogen isotope data exist in the literature fromsome individual gold deposits in the North AmericanCordillera, and much of the hydrogen isotope data is from de-crepitated fluid inclusions that may include secondaries (seeBöhlke and Kistler, 1986; Maheux, 1989; Zhang et al., 1989;Goldfarb et al., 1991b). In this study, 13 samples were col-lected from deposits spanning 30° of latitude from Californiato Alaska and tested for possible relationships between the ni-trogen isotope data and any latitudinal variations of δD in asubset of robust hydrothermal micas. These data, togetherwith a compilation of previous data for individual gold de-posits in the western North American Cordillera, are used toinfer potential source reservoirs for the ore-forming fluids.
Characteristics of Gold-Bearing Quartz Veins in the Western North American Cordillera
The geologic settings and characteristics of gold-bearingquartz vein deposits in the western North AmericanCordillera have been well documented. The principal dis-tricts sampled for this study are described in Böhlke and
Kistler (1986), Taylor (1986, 1987), Weir and Kerrick (1987),and Elder and Cashman (1992; the Mother Lode, California);Leitch et al. (1989, 1991; Bridge River); Church (1997;Greenwood); Mad et al. (1990) and Ash (2001; Stuart Lake),Sketchley et al. (1986), Anderson and Hodgson (1989), andNesbitt et al. (1989; Cassiar); Ash et al. (1996) and Ash (2001;Atlin, British Columbia); Nesbitt et al. (1989) and Rushton etal. (1993; Klondike, Yukon Territory); and Goldfarb et al.(1997; Fairbanks and Willow Creek, Alaska). Here we onlygive a brief summary of the geology of these districts.
Gold-bearing quartz-carbonate vein systems in accretedterranes of the western North American Cordillera are re-lated to major fault zones, which are commonly reactivatedterrane-bounding sutures that developed during accretionand subduction of allochthonous terranes along the continen-tal margin. Mineralization ages range from about 190 to 50Ma, although not all are well established (Fig. 1). This timespan covers much of the evolution of the Cordilleran orogen.
Vein-hosting lithologies vary widely and include ultramafic,mafic, and felsic volcanic rocks, pre- and syntectonic intru-sions, and a variety of oceanic, clastic sedimentary rocks(Table 1). The most common types of host rocks are ophioliticslices and associated clastic units, largely siltstone andgraywacke. Nearly all the units hosting the vein systems havebeen metamorphosed at lower to upper greenschist facies.The veins are dominated by quartz, with lesser amounts ofCa-Fe-Mg carbonate minerals, muscovite, chlorite, albite,and scheelite. Pyrite is the dominant sulfide mineral, withvarying amounts of arsenopyrite, pyrrhotite, tellurides, andbase metal sulfide minerals. In the wall rocks adjoining theveins, hydrothermal alteration patterns are very similar toArchean counterparts (Groves et al., 1998; McCuaig and Ker-rich, 1998; Ash, 2001). The most common hydrothermal al-teration associated with these vein systems is characterized byextensive additions of quartz, carbonate, muscovite, and sul-fide minerals. Alteration mineral assemblages appear to becontrolled mainly by the host rocks; for example, muscovite isassociated with veins in felsic igneous or clastic sedimentaryrocks, whereas Cr-bearing mica is associated with ores inmafic or ultramafic rocks.
Samples and Analytical MethodsIn this study, samples of quartz-carbonate veins with hy-
drothermal micas were collected from mines or open pits thatprovide access to unweathered samples in a vein geometryconstrained in three dimensions. They were from 16 locationsfrom nine of the most important gold mining districts in thewestern North American Cordillera. Sample locations andsimple characteristics are presented in Table 1.
Nitrogen
Elemental nitrogen contents and nitrogen isotope ratios ofmuscovite separates were analyzed using the techniques de-scribed by Jia and Kerrich (1999, 2000). Each pure muscovitesample was finely ground to –250 mesh and loaded into a tincapsule in a clean room. Samples were heated to about1,100°C for 10 min to release structural nitrogen (Bebout andFogel, 1992; Boyd et al., 1993) and oxidized by passing thecombustion products through a bed of chromium trioxide at1,000°C, using a helium carrier gas. Gases were then passed
110 JIA ET AL.
0361-0128/98/000/000-00 $6.00 110
δ15N, δD, AND δ18O OF CORDILLERAN GOLD-QUARTZ VEINS 111
0361-0128/98/000/000-00 $6.00 111
TAB
LE
1. S
umm
ary
of th
e C
hara
cter
istic
s of
Qua
rtz-
Car
bona
te V
ein
Syst
ems
Sam
pled
in th
e W
este
rn N
orth
Am
eric
an C
ordi
llera
Dis
tric
t/Ve
in s
yste
ms/
Vein
loca
tion
Vein
min
eral
Ve
in g
eom
etry
/Te
cton
ostr
atig
raph
ic
Hos
t roc
k ag
e,Ve
in fo
rmat
ion
Gra
nito
ids
Sour
ces
cam
pde
posi
tL
at (
N)
Lon
g (w
)as
sem
blag
eho
st s
truc
ture
terr
ane
litho
logy
(Ma)
(Ma)
Eas
t-ce
ntra
l Ala
ska
Fai
rban
ksC
hris
tina
65°
04' 1
47°
21'
Qua
rtz,
mus
covi
te,
Stee
ply
dipp
ing
Yuko
n-Ta
nana
Ear
ly P
aleo
zoic
92
–85
95–9
01
chlo
rite
, ank
erite
, ve
inle
ts o
r ve
ins
30 c
m
quar
tzite
, Lat
e py
rite
with
min
or
to 1
.5 m
wid
e in
Pa
leoz
oic
schi
st, a
nd
sulfi
des
exte
nsio
nal z
one
mid
-Cre
tace
ous
dior
iteSo
uth-
cent
ral A
lask
aW
illow
Cre
ekF
ern
min
e61
°39
' 14
9°15
'Q
uart
z, m
usco
vite
,Ve
ins
are
near
ver
tical
Pe
nins
ular
L
ate
Pale
ozoi
c sc
hist
66
79–6
61
chlo
rite
, ank
erite
, in
a s
erie
s of
obl
ique
-(W
rang
ellia
an
d L
ate
Cre
tace
ous
pyri
te w
ith m
inor
sl
ip s
truc
ture
sco
mpo
site
terr
ane)
tona
lite
sulfi
des
Wes
t-ce
ntra
l Yuk
on T
erri
tory
Klo
ndik
e di
stri
ctSh
eba
63°
53'
138°
56'
Qua
rtz,
mus
covi
te,
Stee
ply
dipp
ing
vein
sYu
kon-
Tana
naM
id-P
aleo
zoic
-Ear
ly
140–
130
?2
chlo
rite
, cal
cite
, 50
cm
to 2
m w
ide
in
Mes
ozoi
c m
eta-
pyri
te w
ith m
inor
br
ittle
, ext
ensi
onal
zon
ese
dim
enta
ry a
nd
gale
naig
neou
s ro
cks
Nor
ther
nmos
t Bri
tish
Col
umbi
aA
tlin
(1)
Gol
dsta
r 59
°34
' 13
3°42
' Q
uart
z, C
r St
eepl
y di
ppin
g ve
inle
ts
Cac
he C
reek
Lat
e Pa
leoz
oic-
Ear
ly
172–
170
Mid
-Jur
assi
c3,
4(2
) A
nna
59°
33'
133°
37'
mus
covi
te, f
erro
an-
or v
eins
15
cm to
3.5
m
Mes
ozoi
c m
eta-
F
outh
of J
uly
(3)
Surp
rise
59
°31
' 13
3°28
' m
agne
site
, pyr
ite
wid
e in
bri
ttle
faul
t zon
esse
dim
enta
ry, m
afic
and
ba
thol
ith(4
) M
ckee
Cre
ek59
°27
' 13
3°33
' w
ith m
inor
oth
er
ultr
amaf
ic r
ocks
sulfi
des
Nor
ther
n B
ritis
h C
olum
bia
Cas
siar
(1)
Boo
mer
ang
59°
12'
129°
41'
Qua
rtz,
mus
covi
te,
Vein
s ar
e st
eep
to
Sylv
este
r al
loch
ton
Dev
onia
n-E
arly
Tri
assi
c14
0–13
0M
id-
5–7
(2)
Pete
59°
09'
129°
40'
anke
ritic
car
bona
tes,
vert
ical
, gen
eral
ly 1
to
(par
t of t
he S
lide
met
ased
imen
tary
, C
reta
ceou
s py
rite
with
min
or
2 m
wid
e, in
thru
st
Mou
ntai
n te
rran
e)vo
lcan
ic, a
nd u
ltram
afic
C
assi
ar
othe
r su
lfide
szo
nes
rock
sba
thol
ith
ca. 1
00C
entr
al B
ritis
h C
olum
bia
Stua
rt L
ake
belt
Snow
bird
54°
27'
124°
30'
Qua
rtz,
Cr
Vein
lets
15
to 3
0 cm
C
ache
Cre
ekL
ate
Pale
ozoi
c-E
arly
16
5–16
2M
id-J
uras
sic
4, 8
mus
covi
te, f
erro
an-
wid
e di
ppin
g 40
°to
50°
Mes
ozoi
c m
eta-
165–
162
mag
nesi
te, p
yrite
no
rthe
ast i
n br
ittle
se
dim
enta
ry, a
nd
with
min
or o
ther
fa
rult
zone
ultr
amaf
ic r
ocks
sulfi
des
Sout
hwes
tern
Bri
tish
Col
umbi
aB
ridg
e R
iver
(1)
Bra
lorn
e50
°46
' 12
2°49
' Q
uart
z, C
r St
eepl
y di
ppin
g en
(1
) B
ridg
e R
iver
L
ate
Pale
ozoi
c-E
arly
91
–86
Lat
e 9,
10
(2)
Pion
eer
50°
45'
122°
46'
mus
covi
te, a
nker
itic
eche
lon
vein
s 0.
1 to
(2
) C
adw
alle
rM
esoz
oic
(1)
Bra
lorn
e C
reta
ceou
s ca
rbon
ates
, pyr
ite
10 m
wid
e in
bri
ttle
-di
orite
A
lbiti
te d
ikes
w
ith m
inor
oth
er
duct
ile s
hear
zon
es(2
) C
adw
alle
r gr
eens
tone
91–8
6su
lfide
sSo
uthe
rnm
ost B
ritis
h C
olum
bia
Gre
enw
ood
(1)
Impe
rial
49°
07'
118°
59'
Qua
rtz,
Cr
Stee
ply
dipp
ing
vein
lets
Q
uesn
ellia
Pale
ozoi
c-M
esoz
oic
(?)
Jura
ssic
-
11(2
) R
iver
side
49°
06'
118°
58'
mus
covi
te, f
erro
an-
or v
eins
, 5 c
m to
2 m
in
met
aultr
amaf
ic, m
afic
, C
reta
ceou
s m
agne
site
, pyr
itew
idth
and
sedi
men
tary
roc
ksN
elso
n pl
uton
Sout
hern
Cal
iforn
iaM
othe
r L
ode
(1)
Car
son
37°
58'
120°
25"
Qua
rtz,
Cr
Stee
ply
dipp
ing
vein
sSi
erra
Nev
ada
Pale
ozoi
c-M
esoz
oic
147–
144
Mes
ozoi
c-12
–14
(2)
Cou
lterv
ille
37°
43'
120°
12'
mus
covi
te, M
g in
rev
erse
faul
tfo
othi
lls m
etam
orph
ic
met
ased
imen
tary
, 12
5–11
0 (?
)C
reta
ceou
s ca
lcite
, mag
nesi
te,
com
plex
volc
anic
, and
ultr
amfic
Si
erra
Nev
ada
pyri
tero
cks
bath
olith
Sour
ces:
1 =
Gol
dfar
b et
al.
(199
7), 2
= R
usht
on e
t al.
(199
3), 3
= A
sh e
t al.
(199
6), 4
= A
sh (
2001
), 5
= Sk
etch
ley
et a
l. (1
986)
, 6 =
And
erso
n an
d H
odgs
on (1
989)
, 7 =
Dri
ver
et a
l. (2
000)
, 8 =
Mad
uet
al.
(199
0), 9
= L
eitc
h et
al.
(198
9), 1
0 =
Lei
tch
et a
l. (1
991)
, 11
= C
hurc
h (1
997)
, 12
= B
öhlk
e an
d K
istle
r (1
986)
, 13
= L
ande
feld
(19
88),
14 =
Eld
er a
nd C
ashm
an (
1992
)
through a second furnace containing copper at 600°C, whereexcess oxygen was absorbed and nitrogen oxides reduced toelemental nitrogen. Elemental nitrogen concentrations wereobtained from each sample based on system calibration usingknown standards. Analysis of N isotopes on muscovite sepa-rates was conducted using a high-precision, continuous flowisotope ratio mass spectrometer (CF-IRMS) at the Soil Sci-ence Laboratory, University of Saskatchewan. Analytical re-producibilities were ca. ± 0.3 per mil (generally ≤0.3‰ for n≥ 3) for δ15N. The long-term reproducibility for internationalnitrogen isotope standard materials in the laboratory is 0.54 ±0.07 per mil for IAEA-N1 (n = 15, accepted value 0.53‰),20.34 ± 0.08 per mil for IAEA-N2 (n = 10, accepted value
20.41‰), and 5.15 ± 0.21 per mil for the internal laboratorystandard material BLN.SOIL (n = 20, accepted value5.15‰). Ten replicate analyses of the muscovite mineral sep-arate sample CD11-21-1 yielded a mean δ15N value of 3.43(1σ = 0.06‰). Isotope data are reported in standard δ nota-tion relative to atmospheric N2.
Oxygen and hydrogen
Oxygen isotope compositions were determined for 13 se-lected samples using conventional procedures; pure quartzseparates were reacted with bromine BrF5, followed by quan-titative conversion to CO2 (Clayton and Mayeda, 1963). Hy-drogen isotope analyses of 11 selected muscovite separates
112 JIA ET AL.
0361-0128/98/000/000-00 $6.00 112
Alexander
Cassiar
Cache Creek
Bridge River
Chugach
Kootenay
Quesnellia
Stikine
Wrangellia
Yukon-Tanana
Older passivemargin rocks
Slide Mountain
Denali fault system
Tintina fault System
San Andreas fault
DFS:
TFS:
SAF:
Gold Mining Camp
Fairweather-Queen Charlotte faultsFQF:
500 km
North AmericanMargin
Terranes
Craton
U.S.A
Canada
U.S.A
U.S.A
Canad
a
Mexico
49o
32o
Coast B
atholith
Coast R
anges
N
Eastern ed
ge of Cord
illeran Orogen
DFS TFS
FQF
SAF
Accretionary P
rism
Accretionary P
rism
Gold Mining Camps
1. Fairbanks 92-85 Ma
2. Willow Creek 66 Ma
3. Juneau 56-53 Ma
4. Klondike 140-130 Ma
5. Atlin 172-170 Ma
6. Snowbird 165-162 Ma
7. Cassiar 140-130 Ma
9. Bridge River 91-86 Ma
10. Coquihalla (?)
8. Cariboo 140 Ma
12. Alleghany 147 Ma ?
13. Mother Lode 144 Ma ?
13
12
10
8
5
7
4
1
3
6
2
11
11. Greenwood (?)
Sierra Nevada foothills
60o
9
FIG. 1. Distributions of synorogenic gold deposits in the western North American Cordillera. Various terranes are gener-alized from Coney (1989), Wheeler and McFeely (1991), and Monger (1993). Sources for the ages of mineralization in thedifferent districts are indicated in Table 1.
were performed using the uranium technique of Bigeleisen etal. (1952). A Finnigan Mat Delta mass spectrometer was usedfor oxygen in CO2 at the Isotope Laboratory, University ofSaskatchewan, and a Finnigan Mat 252 mass spectrometer atQueens University was used for hydrogen isotopes on mus-covite. Analytical reproducibilities were ±0.2 per mil for δ18Oand ±2.0 per mil for δD. Isotope data are reported in stan-dard δ notation relative to the Vienna SMOW standard forhydrogen and oxygen.
Isotopic Composition of Hydrothermal Minerals
Nitrogen isotope compositions of muscovite
Elemental nitrogen concentrations and δ15N values of hy-drothermal micas from 16 gold-bearing quartz vein systems in
nine mining camps of the western North American Cordilleraare relatively uniform. There is a narrow range within eachvein system, where δ15N typically varies by less than ±0.3 permil, and values between deposits of different mining campstypically overlap (Fig. 2, Table 2). This is well illustrated inthe results from the Christina (Fairbanks) and Fern mine(Willow Creek) vein systems of Alaska, which have mean δ15Nvalues of 5.8 and 5.5 per mil and elemental nitrogen contentsranging from 390 to 401 and 256 to 274 ppm, respectively. Inthe Sheba vein, Klondike district of the Yukon, six muscoviteseparates from quartz veins have a range of δ15N values be-tween 1.6 and 1.8 per mil and elemental nitrogen contents260 and 280 ppm.
In the Cassiar mining camp of northern British Columbiasamples from the Pete vein system (Cr-bearing muscovite)
δ15N, δD, AND δ18O OF CORDILLERAN GOLD-QUARTZ VEINS 113
0361-0128/98/000/000-00 $6.00 113
1 2 3 4 65100
1000
5000
N (
ppm
)
A
15N (‰)
Christina
Atlin
Fern Mine
Cassiar
Klondike
Stuart Lake
Bridge River
Greenwood
Mother Lode
-10 -5 0 5 10 15 20 25
Phanerozoic Au-quartz veinsin the western N.A.Cordillera
10
100
1000
Mantle derived rocks
Organic materials
S-type graniteMetamorphic rocks
Archean Au-quartz veins in Canadaand Western Australia
B
15N (‰)
N (
ppm
)
FIG. 2. A. The N content and δ15N values of hydrothermal muscovite separates from the western North AmericanCordillera quartz vein systems. B. Data compared to those from Archean volcanic- and plutonic rock-dominated terranes inCanada and Western Australia (Jia and Kerrich, 1999, 2000). Fields for rock reservoirs: Organic materials from Peters et al.(1978), Williams et al. (1995), and Ader et al. (1998); metamorphic rocks from Haendel et al. (1986) and Bebout and Fogel(1992); granites from Boyd et al. (1993); mantle-derived rocks from Javoy et al. (1984), Boyd et al. (1987, 1992), Javoy andPineau (1991), Boyd and Pillinger (1994), Marty (1995), Cartigny et al. (1997, 1998), and Marty and Humbert (1997).
and Boomerang vein (white muscovite), which are located 16km apart possess mean δ15N values of 1.9 ± 0.2 (1σ; n = 9) to2.1 ± 0.1 per mil (1σ; n = 6), respectively. Similarly, in theAtlin mining camp, quartz vein systems at the Mckee Creek,Surprise, Goldstar, and Anna deposits spread over about 150km2 and have mean δ15N of 4.5 ± 0.9 per mil (n = 22). For the
Bridge River and Greenwood camps, and the Mother Lodemining camp, more than 1,000 km farther south, the meanδ15N values are 2.9 ± 0.9 (1σ; n = 22), 3.2 ± 0.6 (1σ; n = 9),and 2.7 ± 0.4 per mil (1σ; n = 16), respectively. In summary,at the continent scale, from the Mother Lode in California toFairbanks, Alaska, the total range of δ15N is only 1.6 to 6.1 per
114 JIA ET AL.
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TABLE 2. N Contents and δ15N of Mica Separates from Quartz-Carbonate Vein Systems in the Western North American Cordillera
Location/ Sample Analyzed N content δ15N (‰) Location/ Sample Analyzed N content δ15N (‰)vein system no. mineral (ppm) mean ±1σ vein system no. mineral (ppm) mean ±1σ
Fairbanks, east-central Alaska 5.5 ± 0.28Christina Chr-1 Muscovite 394 5.9
Chr-2 Muscovite 390 5.4Chr-3 Muscovite 401 6.1
Willow Creek, south-central Alaska 5.5 ± 0.35Fern mine Fern-1 Muscovite 274 5.8
Fern-2 Muscovite 260 5.5Fern-3 Muscovite 256 5.1
Klondike, Yukon 1.7 ± 0.08Sheba mine SH-1-1 Muscovite 275 1.6
SH-1-2 Muscovite 270 1.6SH-2-1 Muscovite 280 1.8SH-2-2 Muscovite 280 1.7SH-3-1 Muscovite 270 1.7SH-3-2 Muscovite 260 1.7
Atlin Camp, northernmost British Columbia 4.7 ± 0.87Mckee Creek CAS89.4.1A Cr muscovite 1946 4.6
CAS89.4.1B Cr muscovite 1929 4.8CAS89.4.1C Cr muscovite 1963 4.6CAS89.4.1D Cr muscovite 1926 4.4CAS89.4.1-1 Cr muscovite 1965 4.9CAS89.4.1-2 Cr muscovite 1947 4.7CAS89.4.1-3 Cr muscovite 1981 4.9CAS89.4.1-4 Cr muscovite 1947 4.8
Surprise CAS89.14.2.3-1 Cr muscovite 786 5.8CAS89.14.2.3-2 Cr muscovite 768 5.7CAS89.14.2.3-3 Cr muscovite 767 5.3CAS89.14.2.3-5 Cr muscovite 799 5.6CAS89.14.2.3-6 Cr muscovite 787 5.7CAS89.14.2.3-7 Cr muscovite 786 5.3
Goldstar CAS89.05.02 Cr muscovite 330 3.3CAS89.05.03 Cr muscovite 322 3.2CAS89.05.04 Cr muscovite 326 3.0CAS89.05.05 Cr muscovite 338 4.2CAS89.05.06 Cr muscovite 329 3.3CAS89.05.07 Cr muscovite 333 3.4
Anna CAS89.01.01 Cr muscovite 848 4.3CAS89.01.02 Cr muscovite 827 4.1
Cassiar Camp, northern British Columbina 2.0 ± 0.15Pete PETE3-2-1 Cr muscovite 1616 1.9
PETE3-2-2 Cr muscovite 1666 1.8PETE3-2-3 Cr muscovite 1660 1.8PETE3-1-1 Cr muscovite 2325 2.2PETE3-1-2 Cr muscovite 2664 1.7PETE3-1-3 Cr muscovite 2542 2.1PETE3-1-4 Cr muscovite 2566 2.2PETE3-3-2 Cr muscovite 1635 1.9PETE3-3-3 Cr muscovite 1692 1.7
Boomerang BV-1 Muscovite 743 2.1BV-2 Muscovite 740 2.0BV-3 Muscovite 745 1.9BV-4 Muscovite 741 2.0BV-5 Muscovite 750 2.1BV-6 Muscovite 744 2.2
Stuart Lake, central British Columbia 1.7 ± 0.06Snowbird CAS89.41.1-1 Cr muscovite 3466 1.8
CAS89.41.1-3 Cr muscovite 3434 1.6CAS89.41.1-4 Cr muscovite 3497 1.7CAS89.41.1-6 Cr muscovite 3472 1.7
Bridge River Camp, southwestern British Columbia 2.6 ± 0.90Bralorne mine CAS91.61-1 Cr muscovite 3336 2.0
CAS91.61-2 Cr muscovite 3303 2.0CAS91.61-3 Cr muscovite 3345 2.1CAS91.61-5 Cr muscovite 3368 2.0CAS91.61-6 Cr muscovite 3341 2.3CAS91.61-7 Cr muscovite 3368 2.5CAS91.62-1 Cr muscovite 3255 2.4CAS91.62-3 Cr muscovite 3310 2.2CAS91.62-4 Cr muscovite 3276 2.2CAS91.61-6 Cr muscovite 3331 2.4CAS91.64B Cr muscovite 2573 2.7CAS91.64C Cr muscovite 2593 2.8CAS91.64D Cr muscovite 2579 3.0CAS91.64-1 Cr muscovite 2473 3.1CAS91.64-2 Cr muscovite 2592 2.8CAS91.64-3 Cr muscovite 2609 2.3CAS91.64-4 Cr muscovite 2597 2.9
Pioneer CAS91.66-1 Cr muscovite 930 4.3CAS91.66-2 Cr muscovite 963 4.6CAS91.66-3 Cr muscovite 960 4.7CAS91.66-5 Cr muscovite 977 4.7CAS91.66-6 Cr muscovite 971 4.2
Greenwood, southen British Columbia 3.0 ± 0.60Imperial CAS91.40A1 Cr muscovite 129 2.7
CAS91.40A2 Cr muscovite 131 3.0CAS91.40A3 Cr muscovite 124 2.6CAS91.40A4 Cr muscovite 131 2.8CAS91.40A5 Cr muscovite 131 2.2
Riverside RS-1 Cr muscovite 148 3.8RS-2 Cr muscovite 132 3.7RS-3 Cr muscovite 132 3.5RS-4 Cr muscovite 128 4.0
Mother Lode, southern California 2.7 ± 0.45Carson Hill CH21 Cr muscovite 850 3.0
CH22 Cr muscovite 844 3.2CH23 Cr muscovite 834 2.7CH24 Cr muscovite 837 2.8CH25 Cr muscovite 835 2.6CH26 Cr muscovite 851 2.6CH27 Cr muscovite 832 2.3
Coulterville CT41 Cr muscovite 740 3.4CT42 Cr muscovite 733 3.5CT43 Cr muscovite 734 2.8CT44 Cr muscovite 733 2.3CT45 Cr muscovite 738 2.0CT46 Cr muscovite 729 2.0CT47 Cr muscovite 748 2.8CT48 Cr muscovite 750 2.5CT49 Cr muscovite 745 2.3
mil, with a mean of 3.0 per mil, and elemental nitrogen con-tents span 130 to 3,500 ppm, with a mean of 1,535 ppm (Fig.2, Table 2).
Oxygen and hydrogen isotope compositions of silicates
The range of δ18O values for vein quartz samples collectedand analyzed during this study is 14.6 to 22.2 per mil withinthe limitations of the dataset. There is also uniformity in theδ18O values in individual mining camps (Table 3). Three sam-ples from the Carson Hill and Coulterville deposits in south-ern California have δ18O values between 16.5 and 18.6 permil. Similar isotopic homogeneity of vein quartz is noted inthe Bridge River, Cassiar, and Atlin mining camps, wheremean δ18O values of vein quartz are 18.0, 17.0, and 21.7 permil respectively. For the Sheba vein system, Klondike district,three samples give δ18O values of 14.6 to 15.1 per mil (Table3).
The majority of muscovites are characterized by a narrowrange of δD values from –60 to –110 per mil (Table 3). Twosamples (CH2 and CT4) collected from the Carson Hill andCoulterville veins in the southern Mother Lode (lat 37° N)both yield δD values of –65 per mil. One sample from theBridge River camp in southern British Columbia (lat 50° N)possesses a δD value of –60 per mil. Two samples from theBoomerang vein in the Cassiar camp of northern British Co-lumbia (lat 59° N) yield δD values of –95 per mil, and in theAtlin camp three samples from different vein locations yieldδD values ranging from –66 to –112 per mil. Three samplesfrom the Sheba vein in the Klondike district (lat 63° N) haveδD values ranging from –161 to –172 per mil.
Discussion
Elemental nitrogen concentration and N isotope characteristics
The nitrogen concentrations and nitrogen isotope ratios forhydrothermal micas from the gold-bearing vein systems of
the western North American Cordillera are not consistentwith mantle-derived fluids. Mantle nitrogen concentrationsand isotope compositions have been determined from bothmidocean ridge basalts and from fibrous diamonds in Zaire byJavoy et al. (1984), Javoy and Pineau (1991), and Marty (1995)and extended to a worldwide sampling basis by Boyd et al.(1987, 1992). Their results show that nitrogen contents inmantle-derived materials are very low (<1–2 ppm), and thatδ15N values are negative (–8.7 up to –1.7‰) with a mode of–6 to –5 per mil (Table 4). Studies of fibrous diamonds haveshown that mantle nitrogen appears to be isotopically homo-geneous. The characteristics of the hydrothermal micas aredistinct from mantle materials both in terms of more en-riched δ15N values and high elemental nitrogen contents (Fig.2, Table 2).
The data for hydrothermal micas are also inconsistent withorthomagmatic fluids evolved from a crystallizing granitoid.Boyd et al. (1993) studied granites in southwestern Englandthat have δ15N values between 8.4 and 10.2 per mil (two out-liers of 5.1 and 7.0‰). Granitic rocks, worldwide, also havelow elemental nitrogen contents of 21 to 27 ppm (Table 4;Wlotzka, 1972; Hall, 1999). Collectively, nitrogen isotopecompositions of hydrothermal muscovites from the NorthAmerican Cordillera are depleted in 15N relative to graniticrocks, and their elemental nitrogen contents are higher.
A role for meteoric water in the formation of the mus-covite cannot be ruled out on the basis of the nitrogen iso-tope composition of the hydrothermal micas in the gold-bearing quartz vein systems. Global nitrogen isotope valuesof 4.4 ± 2.0 per mil (n = 263; Owens, 1987) of meteoric wateroverlap with micas in these gold deposits. However, the ele-mental nitrogen contents of meteoric water are very low—<2ηmole (Table 4; Homes et al., 1998)—and in geothermal flu-ids are 0.6 to 2 ηmole (Crittenden, 1981), whereas muchhigher N2 concentrations have been observed and measuredin fluid inclusions from orogenic gold deposits. For example,fluid inclusions in vein quartz of the Dolgellau gold belt innorth Wales contain 0.19 to 0.27 mol percent N2 (Bottrelland Miller, 1990), and significant amounts of N2 in the ore-forming fluids have also been measured from gold depositsin Alaska (Goldfarb et al., 1997) and the Central and NorthDeborah gold mines at Bendigo, Australia (Jia et al., 2000).In crustal metamorphic fluids in orogenic belts, N2 is a mainform of nitrogen, having been reported from a variety offluid inclusion studies, including 1.52 to 55.36 mol percent atnorth Wales (Bottrell et al., 1988), 0.6 to 99.0 mol percent inthe Bastogne (Darimont et al., 1988), and 9.6 to 77.4 molpercent at Mari Rosa (Ortega et al., 1991). Furthermore, inorogenic gold deposits there is clear field evidence, in theform of horizontal veins dilated vertically, for the lithostaticto superlithostatic fluid pressures, ruling out deeply convect-ing meteoric water for which Pfluid ≈ 1/3 Plithostatic (Kerrich andAllison, 1978; Sibson et al., 1988; Kerrich, 1989). In sum-mary, elemental nitrogen contents are generally higher influid inclusions from lode gold deposits than in geothermalfluids. Even if nitrogen contents do not provide a definitivedistinction between meteoric and metamorphic origins ofthe ore-forming fluids, meteoric water can be ruled out fromconsiderations both of hydrodynamics and isotopic shifts ofδD and δ18O.
δ15N, δD, AND δ18O OF CORDILLERAN GOLD-QUARTZ VEINS 115
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TABLE 3. Oxygen and Hydrogen Isotope Data from Gold-Bearing Quartz Veins
δ18O (‰) δD (‰)Vein location Sample no. Quartz Muscovite
Klondike SH-1 15.1 –161SH-2 14.9 –168SH-3 14.6 –172
Atlin CAS89.14.2.3 21.7 –110CAS89.05 21.4 –66CAS89.01 22.2 –112
Cassiar BV-1 17.1 –95BV-4 16.9 –98
Bridge River CAS91.66 17.8 –60CAS91.661 18.1
Mother Lode CH1 18.6CH2 16.5 –65CH21 16.9 –62CT4 17.6 –65
1 Duplicate sample
Elemental nitrogen contents and δ15N values of gold de-posits in the western North American Cordillera are consis-tent with those reported for metasedimentary rocks in theCatalina Schist subduction zone complex of California, whereelemental concentrations of nitrogen are 60 to 2,100 ppm andwhole-rock δ15N values range from 1.6 to 6.0 per mil (n = 123;Bebout and Fogel, 1992; Bebout, 1997), similar to averagePhanerozoic crust (Table 4; Haendel et al., 1986; Williams etal., 1995; Kao and Liu, 2000). They are also comparable todata for the turbidite-hosted Paleozoic quartz-carbonate veinsystems of the Bendigo-Ballarat region in the Tasman orogenof southeastern Australia, where elemental nitrogen concen-trations in muscovite are 652 to 895 ppm and δ15N values are2.8 to 4.5 per mil (Jia et al., 2001).
The geochemical behavior of nitrogen during formation ofgold-bearing quartz veins has not been examined in detail sofar. According to Bottrell and Miller (1990) in a study of blackshale-hosted quartz-bearing vein gold deposits of northWales, leaching of NH+
4 from host rocks by fluids derivedfrom metamorphic dehydration is the most likely source of ni-trogen in the ore fluid. The thermochemical constraints onthe behavior of nitrogen species (NH+
4 and N2) in the fluidsand their transport and deposition during mineralization arecontrolled by pH and fO2 (Bottrell and Miler, 1990, and refer-ences therein). Although the nitrogen content of the hy-drothermal vein micas appears to generally reflect the con-centration of nitrogen in the source rocks, there could be a
number of other factors that can influence the nitrogen con-tent of a hydrothermal mica that are not directly related tothe abundance of nitrogen in the source.
Rock-fluid fractionation
There is no significant nitrogen isotope fractionation be-tween rock (NH+
4) and fluid (N2) during metamorphic dehy-dration. Bebout and Fogel (1992) empirically evaluated fluid-rock isotope fractionation of N2-NH+
4 during devolatilizationof metasedimentary rocks of the Catalina schist belt by pro-gressive metamorphism, using a Rayleigh distillation model,based on direct measurement of nitrogen isotope ratios ofwhole-rock powder. They obtained δ15N of 2.2 ± 0.6 per mil(632 ± 185 ppm N) in lowest grade rocks (300°C) and 4.3 ±0.9 per mil (138 ± 76 ppm N) for high-grade rocks (600ºC).They calculated fluid-rock (N2- NH+
4) nitrogen isotope frac-tionations of –1.5 ± 1 per mil with the Rayleigh distillationequation at temperatures ranging from 350° to 600°C. Ex-perimental studies on metamorphism of sedimentary kerogenshow that although the elemental nitrogen content inmetasedimentary rocks decreases during metamorphism, theisotopic composition does not change up to 600°C (Williamset al., 1995; Ader et al., 1998). Studies by Jia and Kerrich(1999, 2000) on hydrothermal micas in Archean orogenicgold-bearing quartz vein systems, formed during metamor-phism over a range from subgreenschist to amphibolite facies,also show that elemental nitrogen contents of the micas
116 JIA ET AL.
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TABLE 4. Summary of N Contents and N Isotope Compositions in Various Geologic Reservoirs
Reservoirs/ N content δ15N (‰) δ15N (‰)component (ppm) range mean ±1σ Observations References
Mantle-derived materialsMidocean ridge basalts 36 –1.7 to –8.7 –5.0 Fresh basalts 1, 2Midocean ridge basalts 1 to 2 –1. 0 to 6.4 –5.0 Fresh basalts 3, 4Most diamonds 2 to 40 0 to –26 –5.0 P-type diamond 5Most diamonds –1.1 to –10.1 –5.0 E-type diamond 6
Granitic rocksGranites 21 to 27 +5.1 to +10.2 S-type granite 7-9
Organic materialsTerrestrial and aquatic plants –4.4 ± 1.2 Organic compounds 10Terrestrial leaf litter –3.8 ± 0.2 Organic compounds 11Chlorin in sapropels –5.0 ± 0.4 Organic compounds 12Living phytoplankton –6.4 ± 1.4 Organic compounds 12
Marine sedimentary rocksMarine sediments +2.4 to +9.9 Kerogen 13Marine sediments 100 to 2800 3.1 ± 0.3 Kerogen 14Terrestrial sediments +2.7 to +5.1 4.0 ± 0.8 Kerogen 10, 15
Metamorphic rocksMetamorphic rocks 100s to 1000s +3.2 to +7.8 Phanerozoic 16Metasubduction complex 100 to 1100 +1.0 to +6.0 Phanerozoic 17, 18Metamorphic rocks 10s to 100s +11.8 to +17.3 Archean 19
Meteoric waterMeteoric water 2 ηmol 4.4 ± 2.0 Global meteoric H2O 20, 21
Geothermal systemsGeothermal fluids 0.6 to 2 ηmole Geothermal fluids 22
AtmosphereAtmosphere 78 (%) 0 Definition 23
References: 1 = Boyd et al. (1987), 2 = Javoy and Pineau (1991), 3 = Marty (1995), 4 = Marty and Humbert (1997), 5 = Cartigny et al. (1997), 6 = Car-tigny et al. (1998), 7 = Boyd et al. (1993), 8 = Hall (1999), 9 = Wlotzka (1972), 10 = Kao and Liu (2000), 11 = Nadelhoffer and Fry (1988), 12 = Sachs andRepeta (1999), 13 = Peters et al. (1978), 14 = Williams et al. (1995), 15 = Ader et al. (1998), 16 = Haendel et al. (1986), 17 = Bebout and Fogel (1992), 18 =Bebout (1997), 19 = Jia and Kerrich (2000), 20 = Owens (1987), 21 = Homes et al. (1998), 22 = Crittenden (1981), 23 = Hoering (1955)
decrease but the isotopic composition does not change signif-icantly with increasing metamorphic grade. Consequently,the nitrogen isotope composition of N2 in fluids is close tothat of the source rock reservoir.
Secular variation of δ15N
Archean and Phanerozoic orogenic gold vein systems havesimilar characteristics and typically are considered to be prod-ucts of the same type of hydrodynamic system (e.g., Kerrichand Wyman, 1990; Groves et al., 1998). However, the resultsfrom the western North American Cordillera veins are dis-tinct from their Late Archean counterparts in Canada andWestern Australia, which are characterized by relatively lownitrogen concentrations of 20 to 200 ppm but higher δ15N val-ues of 10 to 24 per mil (Jia and Kerrich, 1999, 2000).
Here, we propose that there are variations in the crustalabundance of nitrogen and δ15N values through geologic timedue to progressive sequestering of atmospheric N2 and its cy-cling in the evolving atmosphere-crust-mantle systems.Archean crust had a high median δ15N value of 16 per mil andan average crustal abundance of 30 ppm nitrogen, whereasthe Phanerozoic is characterized by low δ15N values with amedian of 3 per mil and an average crustal abundance ofabout 100 ppm nitrogen (Table 4, and references therein).Micas in orogenic gold deposits reflect the secular trendsinasmuch as the ore-forming fluids sample average crust. Inan earlier compilation, Haendel et al. (1986) showed a trendfrom high nitrogen concentration and low δ15N in greenschistfacies metamorphic rocks to low nitrogen concentration buthigh δ15N in amphibolite and granulite facies terranes. Thistrend was originally interpreted to be due to the loss of nitro-gen and 15N-depleted fluids during progressive metamorphicdehydration. However, the lower grade rocks in this data set
are Phanerozoic, whereas the higher grade rocks are Precam-brian, suggesting that secular variations similar to those de-scribed above may account for the observed trends.
δ18O and δD of the ore-forming fluid
Fluid inclusion studies show that vein-forming fluids fromthe Mother Lode belt, California, the Bralorne mine, and theStuart Lake and Cassiar districts in British Columbia, and theKlondike district, Yukon Territory, generally have low salinity(1–6 wt % NaCl equiv), with varying mole fractions of CO2ranging from 5 to 15 percent. These veins formed at temper-atures between 220° and 400°C, under pressures of 70 to 300MPa, with emplacement depths estimated from about 3 to 12km (Böhlke and Kistler, 1986; Weir and Kerrick, 1987; Gold-farb et al., 1989, 1991b, 1997; Madu et al., 1990; Leitch et al.,1991; Rushton et al., 1993). Accordingly, δ18O values of orefluids in equilibrium with vein quartz were calculated usingthe quartz-water fractionation equation of Matsuhisa et al.(1979), assuming vein formation at 300°C. The δD values ofore fluids in equilibrium with vein muscovite were also esti-mated using extrapolation of water-muscovite fractionationfactors (Suzuoki and Epstein, 1976) down to 300°C, indicat-ing a 40 per mil fractionation.
The calculated δ18OH2O and δDH2O for three samples fromthe Carson Hill and Coulterville deposits in the southernMother Lode are between 9 to 12 and –20 to –15 per mil, re-spectively, which fall within the ranges of δ18OH2O = 8 to 14per mil and δDH2O = –50 to –10 per mil from previous inves-tigations in the district (Fig. 3, Table 5; Kistler and Silberman,1983; Böhlke and Kistler, 1986; Taylor, 1986, 1987). Two sam-ples from Bridge River, British Columbia’s largest gold min-ing camp, give δ18OH2O of 11 to 12 per mil and δDH2O of –15per mil. These results are consistent with those of Maheux
δ15N, δD, AND δ18O OF CORDILLERAN GOLD-QUARTZ VEINS 117
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30
40
50
60
70
10 15
A
Alleghany district
Klondike
CassiarAtlin
Bridge River
Mother Lode
Stuart Lake
Lat
itude
18O (‰)
-20-40-60-100-120
Lat
itude
D (‰)
B
* * * *
-140-160
(1)
** * *(2)
* * **
* * * *
(3)
(4)
(5)
(6)
* Fluid Inclusions 30
40
50
60
70
FIG. 3. Ranges of calculated δ18O (A) and δD (B) values of ore fluids plotted with latitude (data source from Table 5).Note: Closed bars represent this study, open bars represent previous studies from Böhlke and Kistler (1986), Taylor (1986,1987), Maheux (1989), Nesbitt et al. (1989), Madu et al. (1990), Goldfarb et al. (1991b), Leitch et al. (1991), and Rushton etal. (1993). All data from silicates, excepting bulk decrepitation of fluid inclusions with star symbols: (1) Fairview and OroFino (Zhang et al., 1989), (2) Bridge River (Nesbitt et al., 1989), (3) Stuart Lake (Madu et al., 1990), (4) Juneau (Goldfarbet al., 1991b), (5) Cassiar (Nesbitt et al., 1989), (6) Klondike (Rushton et al., 1993).
118 JIA ET AL.
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TAB
LE
5. O
xyge
n an
d H
ydro
gen
Isot
ope
Com
posi
tions
of Q
uart
z-C
arbo
nate
Vei
ns in
the
Wes
tern
Nor
th A
mer
ican
Cor
dille
ra a
nd C
ount
erpa
rts
Wor
ldw
ide
Gol
d pr
ovin
ce/
δ18 O
quar
tz (
‰)1
δ18 O
ore
flui
d (‰
)2δD
ore
flui
d (‰
)2R
efer
ence
sdi
stri
ctVe
in lo
catio
nR
ange
Med
ian
±st
d de
vT
(°C
)R
ange
Ran
ge
Cor
dille
raJu
neau
gol
d be
ltJu
neau
15.2
to 2
0.8
225
~ 37
57
to 1
3–3
5 to
–15
2
Klo
ndik
e, Y
ukon
Ter
rito
rySh
eba
14.6
to 1
5.1
14.9
±0.
25 (
3)7
to 8
–130
to –
120
114
.7 to
15.
115
.0 ±
0.2
(4)
323
±18
8.9
±0.
63
Atli
n, n
orth
ernm
ost B
CSu
peri
se, G
olds
tar,
21.4
to 2
2.2
21.7
±0.
4 (3
)13
to 1
6–6
5 to
–20
1an
d A
nna
Cas
siar
, nor
ther
n B
CB
oom
eran
g16
.9 to
17.
110
to 1
1–5
5 to
–50
1Vo
llaug
and
oth
ers
14.3
to 1
9.2
16.9
±1.
3 (1
8)25
0 ~
300
4
Stua
rt L
ake,
cen
tral
BC
Snow
bird
21.0
to 2
4.2
22.7
±1.
2 (8
)21
0 ~
260
12 to
15
5
Bri
dge
Riv
er, s
outh
ern
BC
Pion
eer
17.8
to 1
8.1
11 to
12
–15
1B
ralo
rne
and
Pion
eer
17.1
to 1
9.4
18.4
±0.
8 (2
2)23
0 ~
350
10 to
13
–38
±18
6, 7
Mot
her
Lod
e, C
alifo
rnia
C
arso
n an
d C
oulte
rvill
e16
.5 to
18.
617
.6 ±
0.8
(5)
9 to
12
–20
to –
151
Oro
Ric
o an
d M
cAlp
ine
15.0
to 1
7.5
17.1
±0.
3 (2
4)30
06
to 1
18
Alle
ghan
y, C
alifo
rnia
Ori
enta
l17
.3 to
19.
425
0 ~
325
8 to
15
–50
to –
109
Tasm
an o
roge
nic
belt
Ben
digo
, Aus
tral
iaC
entr
al a
nd N
orth
Deb
orah
14.4
to 1
7.2
16.3
±0.
7 (2
0)35
0 ±
258
to 1
1–3
7 to
–17
10
Hill
End
gol
d fie
ld, A
ustr
alia
Hill
End
gol
d fie
ld15
.2 to
17.
116
.3 ±
0.5
(20)
420
8 to
12
–49
to –
3611
Bir
imia
n gr
eens
tone
bel
tA
shan
ti, W
est A
fric
aA
shan
ti go
ld b
elt
12.8
to 1
5.6
14.9
±0.
7 (1
4)40
0 ±
509
to 1
2–5
3 to
–37
12
Supe
rior
Pro
vinc
e of
Can
ada
Abi
tibi b
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(1989) and Leitch et al. (1991) who showed that the calcu-lated δ18O and δD values of hydrothermal fluids in equilib-rium with quartz and sericites from many of the deposits atBridge River were 10 to 13 and –38 ± 18 per mil, respectively(Fig. 3, Table 5). Two samples of ore fluids from the Cassiardistrict give δ18O and δD values of 10 to 11 per mil and –55± 5 per mil, and three samples from the Atlin camp yield 13to 16 and –65 to –20 per mil. Three muscovite separates fromthe Sheba vein in the Klondike district have δD values of–170 to –160 per mil (Table 3) and thus probably formedfrom a fluid of about –120 to –130 per mil, a composition de-pleted relative to those characteristics of the other vein micas.
The isotopic composition of the ore-forming fluid for theMother Lode belt and Bridge River, Cassiar, and Atlin goldcamps clusters between δ18O values of 8 and 14 per mil andδD values of –65 and –10 per mil, with vein precipitation at300°C. These values are consistent with estimates for othergold-bearing vein systems elsewhere within the westernNorth American Cordillera (see Table 5, and referencestherein). They are also similar to δ18OH2O values of 8 to 12 permil and δD values of –53 to –17 per mil for other metasedi-mentary rock-hosted gold deposits worldwide (Table 5; Lu etal., 1996; Oberthür et al., 1996; Jia et al., 2001). The range ofδ18OH2O values overlaps with but tends to be higher overallthan δ18OH2O values of 6 to 11 per mil obtained for volcanic-hosted Neoarchean orogenic gold deposits (Table 5; Kerrich,1987; Golding et al., 1989; de Ronde et al., 1992; McCuaigand Kerrich, 1998). The minor difference may reflect slightlyhigher formation temperatures of the Archean lodes and/orevolution of metamorphic fluids in greenstone belts withlower bulk δ18O than for Phanerozoic metasedimentary rocksequences.
The total range in δ18O of 15 to 22 per mil for vein quartzfor all mining districts, collectively spanning over 30° latitudein the western North American Cordillera, is typical for veinquartz from orogenic lode gold metallogenic provinces of allages from Archean to Cenozoic (Table 5; δ18O = 12–22‰;Böhlke and Kistler, 1986; Taylor, 1986, 1987; Curti, 1987;Kerrich, 1987; Golding et al., 1989; Goldfarb et al., 1991b; deRonde et al., 1992; Oberthür et al., 1996; Jia et al., 2001). Thishas been interpreted to reflect the isotopic homogeneity ofthe hydrothermal ore fluids and the similar temperatures ofore formation (McCuaig and Kerrich, 1998; Ridley and Dia-mond, 2000). In contrast, epithermal gold deposits are char-acterized by variable δ18O quartz values, which reflect vari-able degrees of water-rock interaction over a range oftemperatures (see Taylor, 1997, for a review).
Nesbitt et al. (1986, 1989) proposed a model of deep circu-lation of meteoric water along transcurrent faults under con-ditions of low water/rock ratios for Cordilleran lode gold de-posits. This model is based primarily on the observations thatδDH2O values obtained by decrepitating bulk fluid inclusionsfrom some vein quartz were depleted (<–100‰) and appar-ently latitudinally dependent. However, the calculated δDH2Ovalues of ore fluids based on robust silicates from the MotherLode, southern California, to the Atlin and Cassiar in north-ern British Columbia, are neither depleted (–65 to –10‰),nor show any latitudinal control, but rather are suggestive ofmetamorphic fluid sources (Fig. 3, Table 5). It is most likelythat low δD values from bulk extraction of fluid inclusions in
some deposits (Nesbitt et al., 1986, 1989) reflect dominantlysecondary inclusions formed in the presence of meteoricwater during uplift of the deposits (Taylor, 1986, 1987; Pick-thorn et al., 1987; Goldfarb et al., 1991a; McCuaig and Ker-rich, 1998).
Meteoric paleowaters in north British Columbia and YukonTerritory are estimated to have δD values of about –140 permil and δ18O values of about –19 per mil (Taylor 1997). Con-sequently, δ18O in a meteoric ore fluid would have to shift bymore than 27 per mil, from –19 per mil to observed values of+8 per mil, by fluid-rock interaction at low water/rock ratios(< 0.1) at 300°C within sedimentary rock-dominant se-quences of the Cordilleran gold districts. A shift of 27 per milin δ18O would be accompanied by large positive shifts in δD,and the primary meteoric water signature would be lost (Ker-rich, 1987). Furthermore, under such a situation, much of thedescending water will rehydrate metamorphic mineralswithin the uplifting and cooling metamorphic terrane. Theonly way to avoid this is to assume that meteoric fluids werestrongly channeled during downward flow, then pervasivelyinteracted with rock with shifting isotope compositions, andfinally were channeled back into narrow structural conduitsduring upward flow. It is difficult, however, to imagine condi-tions, which could consistently lead to such a mechanism offluid flow (Goldfarb et al., 1993). Further, it seems unlikelythat all orogenic gold vein-forming fluids in the Cordillera, aswell as those from elsewhere in the world, could be shiftedfrom variably 18O-depleted meteoric water values dependingon latitude to a much narrower range of δ18O values of 8 to 10per mil (Kerrich, 1989).
An additional complexity in the meteoric water model forCordilleran deposits is constraining the latitude at the timethe deposits formed and distance from the paleo-Pacificocean, given the allochthonous character of the host terranes.Latitude and distance from the ocean are the two factors thatprimarily control the present-day δD of meteoric water onthe North American continent (Taylor, 1997). Cordillerangold provinces from the Mother Lode in southern California,through deposits in the Canadian Cordillera and southeasternAlaska, to Fairbanks, Alaska, and Klondike, Yukon, are ofJurassic to Cenozoic ages (147–53 Ma). From paleomagneticand geologic data these allochthonous terranes have trans-lated along the western margin of North America before orafter the deposits formed. At 100 to 90 Ma, the Interior do-main comprising much of interior British Columbia, centralYukon, and eastern and central Alaska was situated at the lat-itude of northern California. The Coast domain, includingsoutheastern Alaska, much of the Coast Ranges and islands ofBritish Columbia, and the Coast Cascade Mountains of Wash-ington, was situated at latitude similar to northern Mexico.Subsequently, both domains moved northward about 3,000km, reaching their present locations before 45 Ma (Fig. 4;Irving et al., 1995, 1996; Wynne et al., 1995; Ward et al.,1997).
Anomalous δD values of –160 to –170 per mil for mus-covite from the Sheba vein in the Klondike camp are lowcompared to those from other vein systems analyzed in thewestern North American Cordillera (Fig. 3, Table 3). How-ever, as pointed out by Taylor (1986, 1987) and Taylor et al.(1991), hydrothermal micas associated with gold veins in
δ15N, δD, AND δ18O OF CORDILLERAN GOLD-QUARTZ VEINS 119
0361-0128/98/000/000-00 $6.00 119
British Columbia and the Yukon Territory may be character-ized by a range of isotopically primary, enriched, and sec-ondary, depleted values. Our petrographic study of thesemicas from the Sheba vein clearly shows recrystallization.The compositions of these micas are characterized by rela-tively higher H2O contents of 7 to 13 wt percent and low K2Ocontents of 5 to 6 wt percent, with high Si/Al ratios, com-pared to those analyzed from the Mother Lode, BridgeRiver, Cassiar, and Atlin mining camps, with low H2O con-tents of 3.95 to 6.42 percent and high K2O contents of 10.07
to 11.30 wt percent, with low Si/Al ratios (Jia, 2002). Accord-ingly, depleted δD values in the Sheba vein are best inter-preted as reflecting retrograde isotopic exchange accompany-ing compositional change during regional uplift betweenoriginally D-enriched micas and depleted meteoric water.
ConclusionsDetailed studies of the stable isotope systematics (N, H,
and O) of hydrothermal quartz vein systems from differentmining camps in the western North American Cordillera,
120 JIA ET AL.
0361-0128/98/000/000-00 $6.00 120
60
55
49
42
32
U.S.AMexico
U.S.A
Canada
U.S.A
Tintina faultsystem
thrust belt
Eastern limitof Cordilleran
batholithIdaho
Klamathorogen
Nevadabatholith
Sierra
blockSalinian
Peninsular Rangesbatholith
VancouverIsland
BajaCalifornia
San Andreasfault
Denali faultsystem Can
ada
70
60
50
40
30
Canad
aU.S.A
CanadaU.S.A
U.S.AMexico
Intra-Quesnelliafault
batholithIdaho
Nevadabatholith
Sierra
blockSalinian
Peninsular Rangesbatholith
VancouverIsland
BajaBritish Columbia
Baja BritishColumbia fault
Creraceous plutonic belts
Intermontane Superterrane
Coast Mountains orogen
BA
Insular Superterrane
Franciscan Complex
Great Valley Group
Pre-CretaceousKlamath-Sierran terranes
Gold districts
Fairbanks
Willow Creek
Juneau Atlin (170)
Polaris-Taku (63)
Cariboo
Bridge River(91-86)
Greenwood
Mother Lode
(92-77)
(66)
(56-53)
(140)
(147-144)
thrust belt
Eastern limitof Cordilleran
Klondike(140)
Cassiar (140-110)
StuartLake (165)
FIG. 4. A. Present geographic positions of major crustal and tectonic elements of the western North American Cordillera,including the Insular and Intermontane superterranes and the distribution and ages of gold districts. Present-day latitudesare indicated. Terranes are modified from Cowan et al. (1997) and Ward et al. (1997). B. Paleogeographic reconstruction forLate Cretaceous (75–85 Ma). The paleolatitudes for the North American Cordillera at this time are also shown from Wardet al. (1997).
spanning more than 30° latitude, lead to the followinginterpretations:
1. Elemental nitrogen contents and δ15N values of hy-drothermal micas are between 130 and 3,500 ppm and 1.7and 5.5 per mil. This rules out a mantle (low N contents of1–2 ppm and δ15N = –5‰) or granitic fluid sources (N con-tents of 21–27 ppm and δ15N = 6–10‰) but is consistent withfluids derived from metamorphic dehydration reactions ofthe Phanerozoic subduction-accretion complexes, with δ15Nvalues of 1 to 6 per mil.
2. Vein quartz δ18O values are between 14.6 and 22.2 permil but for individual vein systems are strikingly uniform,varying less than ±1 per mil from average values. This impliesboth uniform δ18OH2O and uniform temperatures of precipi-tation for the ore deposits.
3. The δ18O values of gold-bearing vein-forming fluid arecalculated between 8 and 16 per mil (assuming 300°C) andδD values from –10 to –65 per mil, consistent with a deepcrustal source for the ore-forming fluids, most likely of meta-morphic origin.
4. The δD values of ore fluids do not show any latitudinalcontrol, which strongly discounts the meteoric water modelfor these gold deposits. The low δD range of –120 to –130 permil for the Sheba vein in the Klondike district reflects sec-ondary postcrystallization reequilibration between the micasand meteoric waters.
Collectively, the nitrogen, hydrogen, and oxygen stable iso-tope data provide a basis for constraining potential sourcereservoirs for the vein-forming fluids in the western NorthAmerican Cordillera. These are considered to be consistentwith a metamorphic origin, involving derivation of the vein-forming fluids from midcrustal levels by metamorphic dehy-dration reactions at the greenschist to amphibolite transition(Kerrich and Fryer, 1979; Powell et al., 1991). A dilute, aque-ous-carbonic, and N-bearing composition (C-O-H-N) for thevein-forming fluids is similar to that proposed for metamor-phic fluids (Casquet, 1986; Bottrell et al., 1988; Ortega et al.,1991).
AcknowledgmentsWe are grateful to Myles Stocki for assistance with the ni-
trogen analyses, T. Prokopiuk for assistance with oxygen iso-tope analysis in the Department of Geological Sciences, Uni-versity of Saskatchewan, and C. H. Ash and A. Panteleyev forproviding some of the Canadian Cordillera samples. Y. Jia ac-knowledges receipt of a University of Saskatchewan graduatescholarship, a Hugh E. McKinstry grant, the student researchgrant from the Society of Economic Geologists Foundation,and a National Science and Engineering Research Council(NSERC) postdoctoral fellowship. R. Kerrich acknowledgesan NSERC research grant, an NSERC MFA grant, and theGeorge McLeod endowment to the Department of Geologi-cal Sciences, University of Saskatchewan. We thank M. Han-nington, the journal editor, and two journal reviewers, J. Rid-ley and B. Taylor, for their insightful critique of themanuscript and suggestions for improvement.
November 29, 2001; October 16, 2002
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