skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Fluid Mixing and Spatial Geochemical Variability in the Lost City Hydrothermal Field Chimneys
Abstract Carbonate‐brucite chimneys are a characteristic of low‐ to moderate‐temperature, ultramafic‐hosted alkaline hydrothermal systems, such as the Lost City hydrothermal field located on the Atlantis Massif at 30°N near the Mid‐Atlantic Ridge. These chimneys form as a result of mixing between warm, serpentinization‐derived vent fluids and cold seawater. Previous work has documented the evolution in mineralogy and geochemistry associated with the aging of the chimneys as hydrothermal activity wanes. However, little is known about spatial heterogeneities within and among actively venting chimneys. New mineralogical and geochemical data (87Sr/86Sr and stable C, O, and clumped isotopes) indicate that the brucite and calcite precipitate at elevated temperatures in vent fluid‐dominated domains in the interior of chimneys. Exterior zones dominated by seawater are brucite‐poor and aragonite is the main carbonate mineral. Carbonates record mostly out of equilibrium oxygen and clumped isotope signatures due to rapid precipitation upon vent fluid‐seawater mixing. On the other hand, the carbonates precipitate closer to carbon isotope equilibrium, with dissolved inorganic carbon in seawater as the dominant carbon source and have δ13C values within the range of marine carbonates. Our data suggest that calcite is a primary mineral in the active hydrothermal chimneys and does not exclusively form as a replacement of aragonite during later alteration with seawater. Elevated formation temperatures and lower87Sr/86Sr relative to aragonite in the same sample suggest that calcite may be the first carbonate mineral to precipitate.  more » « less
Award ID(s):
1536702
PAR ID:
10492578
Author(s) / Creator(s):
 ;  ;  ;  ;  ;  
Publisher / Repository:
DOI PREFIX: 10.1029
Date Published:
Journal Name:
Geochemistry, Geophysics, Geosystems
Volume:
25
Issue:
2
ISSN:
1525-2027
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. Abstract The Von Damm vent field (VDVF) on the Mid-Cayman Rise in the Caribbean Sea is unique among modern hydrothermal systems in that the chimneys and mounds are almost entirely composed of talc. We analyzed samples collected in 2020 and report that in addition to disordered talc of variable crystallinity, carbonates are a major class of mineral at VDVF. The carbonate minerals include aragonite, calcite, magnesium-rich calcite, and dolomite. Talc and carbonate mineral textures indicate that, rather than replacing volcanic host rock, they precipitate from the mixing of hydrothermal fluids and seawater at the seafloor, occurring in chimneys and surrounding rubble. Alternating precipitation of this mineral assemblage is pervasive, with carbonate minerals typically being succeeded by talc, and with indications that in some cases talc and carbonate minerals replace one another. Stable carbon isotopic data indicate the carbonate minerals originate from the mixing of seawater and hydrothermal fluid, which is supported by U-Th data. Radiocarbon calcite ages and talc 234U-230Th isochron ages indicate mineral ages spanning over thousands to tens of thousands of years. Analyses of these samples illustrate a dynamic system that transitions from carbonate-dominated to Mg-silicate–dominated precipitation over time scales of thousands of years. Our observations raise questions regarding the eventual fate of seafloor precipitates and whether carbonate and silicate minerals in such settings are sequestered and represented in the rock record. 
    more » « less
  2. Abstract Although the serpentinite‐hosted Lost City hydrothermal field (LCHF) was discovered more than 20 years ago, it remains unclear whether and how the presence of microbes affects the mineralogy and textures of the hydrothermal chimney structures. Most chimneys have flow textures comprised of mineral walls bounding paleo‐channels, which are preserved in inactive vent structures to a varying degree. Brucite lines the internal part of these channels, while aragonite dominates the exterior. Calcite is also present locally, mostly associated with brucite. Based on a combination of microscopic and geochemical analyses, we interpret brucite, calcite, and aragonite as primary minerals that precipitate abiotically from mixing seawater and hydrothermal fluids. We also observed local brucite precipitation on microbial filaments and, in some cases, microbial filaments may affect the growth direction of brucite crystals. Brucite is more fluorescent than carbonate minerals, possibly indicating the presence of organic compounds. Our results point to brucite as an important substrate for microbial life in alkaline hydrothermal systems. 
    more » « less
  3. Abstract Modern and ancient lacustrine carbonate build‐ups provide uniquely sensitive sedimentary and geochemical records for understanding the interaction between tectonics, past climates, and local and regional scale basin hydrology. Large (metre to decametre), well‐developed carbonate mounds in the Green River Formation have long been recognized along the margins of an Eocene lake, known as Lake Gosiute. However, their mode of origin and significance with respect to palaeohydrology remain controversial. Here, new sedimentological, Sr isotope data and structural evidence show that significant spring discharge led to the formation of a decametre size complex of shoreline carbonate mounds in the upper Wilkins Peak Member of the Green River Formation at Little Mesa and adjacent areas in the Bridger Basin, Wyoming, USA. Sedimentological evidence indicates that spring discharge was predominantly subaqueous but was, at times, also subaerial, which produced tufa cascades and micro‐rimstone dam structures. The87Sr/86Sr ratios measured from these subaerial spring deposits are less radiogenic (87Sr/86Sr = 0.71040 to 0.71101) than contemporaneous palaeolake carbonates (87Sr/86Sr = 0.71195 to 0.71561) because their parent groundwaters likely interacted with less‐radiogenic Palaeozoic carbonate. Calcite‐cemented sandstone cones and spires (87Sr/86Sr = 0.71037 to 0.71057) in the Wasatch Formation directly below the spring deposits suggest that groundwaters derived from Palaeozoic carbonates preferentially flowed along thrust faults. These results imply that high spring discharge coincided with lake high stands of the upper Wilkins Peak Member, suggesting that recharge at the north‐west margin of the Bridger Basin contributed to Lake Gosiute’s water budget and lowered the salinity of an underfilled, evaporative lake basin. The findings of this study provide criteria for the recognition of groundwater discharge in palaeolake systems which may lead to the discovery of palaeospring systems in other ancient lake deposits. 
    more » « less
  4. Abstract Most Earth surface carbonates precipitate out of isotopic equilibrium with their host solution, complicating the use of stable isotopes in paleoenvironment reconstructions. Disequilibrium can arise from exchange reactions in the DIC‐H2O system as well as during crystal growth reactions in the DIC‐CaCO3system. Existing models account for kinetic isotope effects (KIEs) in these systems separately but the models have yet to be combined in a general framework. Here, an open‐system box model is developed for describing disequilibrium carbon, oxygen, and clumped (Δ47, Δ48, and Δ49) isotope effects in the CaCO3‐DIC‐H2O system. The model is used to simulate calcite precipitation experiments in which the fluxes and isotopic compositions of CO2and CaCO3were constrained. Using a literature compilation of equilibrium and kinetic fractionation factors, modeledδ18O and Δ47values of calcite are in good agreement with the experimental data covering a wide range in crystal growth rate and solution pH. This relatively straightforward example provides a foundation for adapting the model to other situations involving CO2absorption (e.g., corals, foraminifera, and high‐pH travertines) or degassing (e.g., speleothems, low‐pH travertines, and cryogenic carbonates) and/or mixing with other dissolved inorganic carbon sources. 
    more » « less
  5. Abstract Decades of research have resulted in characterization of the ocean floor manifestations of mid‐ocean ridge (MOR) hydrothermal systems, yet numerical models accounting for the connections between heat transfer, hydrology and geochemistry have been slow to develop. The Thermo‐hydro‐chemical code ToughReact can be used to describe the coupled effects of fluid flow, heat transfer, and fluid‐rock chemical interactions that occur in MOR systems. We describe the results of 2‐dimensional simulations of steady state flow in fractured diabase with mineral‐fluid chemical reactions. Basal heating and specified permeability yield maximum temperature of 400°C. Total fluid flux and high fracture flow velocities are in accord with observations. Fluid chemistry, mineralogical changes and87Sr/86Sr ratios can be compared to observations to assess and calibrate models. Simulated high temperature fracture fluids have Mg and SO4near zero, elevated Ca and87Sr/86Sr of about 0.7040. Total alteration is 10%–50% for simple models of spreading. Anhydrite forms mainly near the base of the upwelling zone and results in substantial local fracture porosity reduction. A calibrated model is used to predict how Sr isotopes and other features of altered oceanic crust would be different in the Cretaceous (95 Ma) early Proterozoic (1,800 Ma) and Archean (3,800 Ma), when seawater may have had high Ca and Sr concentrations, lower pH, higher temperature, and lower Na, Mg, and SO4. The simulations are offered as a start on what ultimately may require a longer‐term community effort to better understand the role of MOR thermo‐hydro‐chemical systems in Earth evolution. 
    more » « less