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Abstract Metal stable isotopes (e.g., Zn, Cd, and Cu) have been used to track metal sources in different types of hydrothermal systems. However, metal isotopic variations in sulphides could be triggered by various factors such as mineral precipitation and fluid mixing. Thus, tracking the metal sources of hydrothermal systems is still a big challenge for metal isotopes. In this study, we investigated the Cd isotopic systematics of sphalerite from the Nayongzhi Zn–Pb deposit, which is a Mississippi Valley‐type (MVT) deposit in the Sichuan–Yunnan–Guizhou mineralization province (SYGMP). We reinterpreted the published S isotope data for the SYGMP and found that the large S isotopic variations were controlled by Rayleigh fractionation between sulphide and reduced S. As such, a model that involves mixing of a metal‐rich fluid with a reduced S pool formed by thermochemical sulfate reduction (TSR) can explain the ore formation in the Nayongzhi deposit. Based on this model, no Cd isotopic fractionation was observed due to its low solubility in fluids during mixing, and thus the Cd isotopic variations of sphalerite were inherited from the source rocks. The large range of Zn/Cd ratios and uniform Cd isotopic compositions of the sulphides are similar to those of igneous rocks but different from those of sedimentary rocks, indicating that Zn and Cd were derived mainly from basement rocks (e.g., migmatite, gneiss, and granulite). Our results reaffirm that metal stable isotopes, particularly Cd isotope compositions of sphalerite, are powerful geochemical tracers for investigating the formation mechanisms of ore deposits.

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 lower 87Sr/86Sr relative to aragonite in the same sample suggest that calcite may be the first carbonate mineral to precipitate.

Abstract Post‐orogenic back‐arc magmatism is accompanied by hydrothermal ore deposits and mineralizations derived from mantle and crustal sources. We investigate Zannone Island (ZI), back‐arc Tyrrhenian basin, Italy, to define the source(s) of mineralizing hydrothermal fluids and their relationships with the regional petrological‐tectonic setting. On ZI, early Miocene thrusting was overprinted by late Miocene post‐orogenic extension and related hydrothermal alteration. Since active submarine hydrothermal outflow is reported close to the island, Zannone provides an ideal site to determine the P‐T‐X evolution of the long‐lived hydrothermal system. We combined field work with microstructural analyses on syn‐tectonic quartz veins and carbonate mineralizations, X‐ray diffraction analysis, microthermometry and element mapping of fluid inclusions (FIs), C, O, and clumped isotopes, and analyses of noble gases (He‐Ne‐Ar) and CO2 content in FIs. Our results document the evolution of a fluid system of magmatic origin with increasing mixing of meteoric fluids. Magmatic fluids were responsible for quartz veins precipitation at ∼125 to 150 MPa and ∼300°C–350°C. With the onset of extensional faulting, magmatic fluids progressively interacted with carbonate rocks and mixed with meteoric fluids, leading to (a) host rock alteration with associated carbonate and minor ore mineral precipitation, (b) progressive fluid neutralization, (c) cooling of the hydrothermal system (from ∼320°C to ∼86°C), and (d) embrittlement and fracturing of the host rocks. Both quartz and carbonate mineralizations show noble gases values lower than those from the adjacent active volcanic areas and submarine hydrothermal systems, indicating that the fossil‐to‐active hydrothermal history is associated with the emplacement of multiple magmatic intrusions.

Abstract Travertine deposits preserve an invaluable record of both ancient and modern fluid flow. The goal of this study is to reconstruct spatial and temporal patterns in travertine deposition associated with tectonic and climatic controls along the Lucero Uplift in New Mexico, USA. Uranium‐series ages of travertine deposits in the Lucero Uplift range from 0.94 ± 0.01 to 592 ± 110 ka, indicating that travertine formation has been episodically active since at least ∼600 ka. We find minimal evidence to attribute glacial and interglacial cycles to travertine formation in the Lucero Uplift. δ13C values in travertine deposits range from 2‰ to 9‰ (Vienna Pee Dee Belemnite), δ18O values range from 21‰ to 25‰ (Vienna Standard Mean Ocean Water). Positive correlation between travertine δ13C and δ18O values indicate travertine formation is closely associated with various degrees of CO2 degassing. 87Sr/86Sr values in travertine deposits range from 0.714 to 0.717 and (234U/238U)i values exhibit a remarkably wide range from 3.6 to 9.3, indicative of fluid‐rock interaction during deep crustal circulation in more radiogenic basement rocks. Reconstructed δ13C, δ18O, and (234U/238U)i values in the inferred deep fluid sources showed systematic variations with travertine formation ages, while 87Sr/86Sr values remain relatively constant. Based on dating of undeformed travertine deposits, which overlie tilted Santa Fe Group units, and high (234U/238U)i we infer that the Santa Fe fault has not produced a ground‐rupturing earthquake within the last 490 ± 52 to 592 ± 110 ka (2σ). Our study suggest that travertine formation is driven by fluid flow facilitated by tectonic and mantle structures.

Abstract Microfluidics is a continuously growing field with potential not only in the fields of medical, chemical, and bioanalysis, but also in the domains of optics and information technology. Here, a pressure‐driven 3D microfluidic chip is demonstrated with multiple logic Boolean functions. The presence and absence of fluid at the output of the gates represent the binary signals 1 and 0, respectively. Therefore, the logic gates do not require a specially functionalized liquid to operate. The chip is based on a multilevel of poly(methyl methacrylate) (PMMA)‐based polymeric sheets with aligned microchannels while a flexible polyimide‐based sheet with a cantilever‐like structure is embedded to enable a one‐directional flow of the liquid. Several Boolean logic functions are realized (AND, OR, and XOR) using different fluids in addition to a half adder digital microfluidic circuit. The outputs of the logic gates are designed to be at different heights within the 3D chip to enable different pressure drops. The results show that the logic gates are operational for a specific range of flow rates, which is dependent on the microchannel dimensions, surface roughness, and fluid viscosity and therefore on their hydraulic resistance. The demonstrated approach enables simple cascading of logic gates for large‐scale microfluidic computing systems.