Depositional facies and aqueous-solid geochemistry of travertine-depositing hot springs (Angel Terrace, Mammoth Hot Springs, Yellowstone National Park, USA)
Bw. Fouke et al., Depositional facies and aqueous-solid geochemistry of travertine-depositing hot springs (Angel Terrace, Mammoth Hot Springs, Yellowstone National Park, USA), J SED RES, 70(3), 2000, pp. 565-585
Petrographic and geochemical analyses of travertine depositing hot springs
at Angel Terrace, Mammoth Hot Springs, Yellowstone National Park, have been
used to define five depositional facies along the spring drainage system.
Spring waters are expelled in the vent facies at 71 to 73 degrees C and pre
cipitate mounded travertine composed of aragonite needle botryoids. The apr
on and channel facies (43-72 degrees C) is floored by hollow tubes composed
of aragonite needle botryoids that encrust sulfide-oxidizing Aquificales b
acteria. The travertine of the pond facies (30-62 degrees C) varies in comp
osition from aragonite needle shrubs formed at higher temperatures to ridge
d networks of calcite and aragonite at lower temperatures. Calcite "ice she
ets", calcified bubbles, and aggregates of aragonite needles ("fuzzy dumbbe
lls") precipitate at the air-water interface and settle to pond floors. The
proximal-slope facies (28-54 degrees C), which forms. the margins of terra
cette pools, is composed of arcuate aragonite needle shrubs that create sma
ll microterracettes on the steep slope face. Finally, the distal-slope faci
es (28-30 degrees C) is composed of calcite spherules and calcite "feather"
crystals.
Despite the presence of abundant microbial mat communities and their observ
ed role in providing substrates for mineralization, the com positions of sp
ring-water and travertine predominantly reflect abiotic physical and chemic
al processes, Vigorous CO2 degassing causes a +2 unit increase in spring wa
ter pH, as well as Rayleigh type covariations between the concentration of
dissolved inorganic carbon and corresponding delta(13)C. Travertine delta(1
3)C and delta(18)O are nearly equivalent to aragonite and calcite equilibri
um values calculated from spring water in the higher-temperature (similar t
o 50-73 degrees C) depositional facies. Conversely, travertine precipitatin
g in the lower-temperature (< similar to 50 degrees C) depositional facies
exhibits delta(13)C and delta(18)O values that are as much as 4%0 less than
predicted equilibrium values, This isotopic shift may record microbial res
piration as well as downstream transport of travertine crystals, Despite th
e production of H2S anti the abundance of sulfide-oxidizing microbes, preli
minary delta(34)S data do not uniquely define the microbial metabolic pathw
ays present in the spring system. This suggests that the high extent of CO2
degassing and large open-system solute reservoir in these thermal systems
overwhelm biological controls on travertine crystal chemistry.