TRACE-ELEMENT MOBILITY AND LITHIUM ISOTOPE-EXCHANGE DURING HYDROTHERMAL ALTERATION OF SEA-FLOOR WEATHERED BASALT - AN EXPERIMENTAL-STUDY AT350-DEGREES-C, 500 BARS
We. Seyfried et al., TRACE-ELEMENT MOBILITY AND LITHIUM ISOTOPE-EXCHANGE DURING HYDROTHERMAL ALTERATION OF SEA-FLOOR WEATHERED BASALT - AN EXPERIMENTAL-STUDY AT350-DEGREES-C, 500 BARS, Geochimica et cosmochimica acta, 62(6), 1998, pp. 949-960
The relative mobility of trace incompatible elements and exchange of l
ithium isotopes during alteration of basalt previously altered by expo
sure to seawater at low temperatures (seafloor weathered) were experim
entally determined at 350 degrees C, 500 bars. These data are importan
t as a means to test models calling for hydrothermal alteration of wea
thered basalt as a source of alkali elements for hot spring Vent fluid
s at mid-ocean ridges. Weathered basalt used for the experiment was ch
aracterized by high Cs, Rb, B, K, and Li concentrations, high Cs/Rb, a
nd low K/Rb and Ba/Rb ratios, respectively, relative to fresh basalt.
The basalt is enriched in Li-7 consistent with a history involving Li
uptake during seafloor weathering. The experiment involved a Na-Ca-K-C
l fluid and flexible cell hydrothermal equipment, which permitted peri
odic sampling of the fluid phase at experimental conditions. The extra
ction efficiency of all trace incompatible elements was significant an
d ranged from 40 to 80%. Cesium, rubidium, lithium, and boron were par
ticularly mobile, whereas Ba, Sr, and to a lesser degree, K were taken
up by alteration minerals. Early stage release of Li was dominated by
Li-7, most probably as a consequence of the dissolution of low temper
ature alteration phases in the weathered basalt that were rendered uns
table at the elevated temperatures of the experiment. Subsequently, ho
wever, an increase in Li-6 in solution was observed owing to a combina
tion of mineral dissolution (from Li-bearing components in fresh basal
t) and isotopic equilibration effects. Owing to the mobility of Li dur
ing hydrothermal alteration of weathered basalt, it is unlikely that d
issolution of weathered basalt components in subseafloor reaction zone
s (350-400 degrees C) could occur without noticeably affecting the lit
hium isotope composition of vent fluids, as inferred previously from f
ield studies. Thus, the relatively high Cs/Rb ratios of some vent flui
ds, which were thought to be the result of hydrothermal alteration of
weathered basalt, may be caused by other effects, such as partitioning
of Rb relative to Cs into hydrothermal minerals at temperatures in ex
cess of 400 degrees C. Cs/Rb ratios in vent fluids from a wide range o
f Pacific and Atlantic-ridge localities, however, reveal relatively la
rge variations in space and time, which suggest that a single process
is unlikely to account for all of the data. The relative mobility of t
race alkali elements in weathered basalt not only constrains models of
alkali element enrichment in hot spring vent fluids at mid-ocean ridg
es, but also provides data bearing on potential sources of alkali elem
ents for are magmas in subduction zones. Copyright (C) 1998 Elsevier S
cience Ltd.