Ms. Appold et al., SULFUR ISOTOPE AND FLUID INCLUSION CONSTRAINTS ON THE GENESIS OF MISSISSIPPI VALLEY-TYPE MINERALIZATION IN THE CENTRAL APPALACHIANS, Economic geology and the bulletin of the Society of Economic Geologists, 90(4), 1995, pp. 902-919
Mississippi Valley-type mineralization from two major host formations
in the central Appalachians was studied in order to gain a better unde
rstanding of depositional conditions, sources of ore constituents, and
the distribution of mineralizing fluids in the region. Sulfur isotope
data obtained in this study and fi om the literature (Ault and Kulp,
1960; Howe, 1981; Crawford and Beales, 1983; LeHuray, 1984; Wilbur et
al., 1990) show that mineralization in each formation acquired sulfur
from sources of similar isotopic composition. Barite deposits in the B
eekmantown Group have delta(34)S values ranging from 25 to 36 per mil;
the values probably closely reflect the isotopic composition of die s
ulfur-bearing fluid involved in the barite formation. Sulfide deposits
in this formation have more variable compositions and more complex is
otopic systematics. In both the Timberville district and Nittany Arch
area, main-stage sulfide minerals have delta(34)S values ranging from
about 15 to 30 per mil. Each district also has a smaller, isotopically
lighter substage of sphalerite mineralization that has delta(34)S val
ues between 1 and 19 per mil. Sulfate minerals in the Nittany Arch are
a are isotopically heavier than the sulfides, with delta(34)S values b
etween 30 and 40 per mil. The lightest sulfur in the central Appalachi
an Mississippi Valley-type districts is found in the Friedensville dis
trict, where delta(34)S values of sulfide minerals range between -9 an
d +1 per mil. Sulfide minerals from the two Silurian Tuscarora-Shawang
unk-hosted deposits have similar delta(34)S values of 21 to 35 per mil
, Minor amounts of sulfate minerals in this formation are isotopically
heavy with delta(34)S values between 34 and 43 per mil. New fluid inc
lusion data were also obtained from the Timberville district and revea
l the presence of at least two distinct fluids involved in mineralizat
ion-a more saline or calcium-rich fluid with final melting temperature
s between -42 degrees and -29 degrees C, and a less saline or more cal
cium-poor fluid with final melting temperatures of -24 degrees to -12
degrees C. Homogenization temperatures of both inclusion types ranged
for the most part between 100 degrees and 170 degrees C. Geologic evid
ence suggests that the Beekmantown Group and Tuscarora-Shawangunk Form
ations were part of distinct paleoaquifers, and together with the sulf
ur isotope data, also suggests that the source of sulfur for Mississip
pi Valley-type deposits in each paleoaquifer was connate (formational)
fluids derived from seawater, or alternatively in the case of the Bee
kmantown Group, intraformational evaporites. Furthermore, evidence of
mixing and a temporal increase in the oxidation state of mineralizing
conditions in at least two of the districts suggests that much of the
Mississippi Valley-type mineralization in the central Appalachian regi
on may be the result of mixing of oxidizing tectonically driven Zn-Pb
or Ba-rich fluids with sulfur-rich fluids of varying oxidation state p
resent in the Beekmantown Group and Tuscarora-Shawangunk Formations.