The ultramafic-hosted Kairei vent field is located at 25°19′ S, 70°02′ E, towards the Northern end of segment 1 of the Central Indian Ridge (CIR-S1) at a water depth of ~2450 m. This study aims to investigate the distribution of trace elements among sulfide minerals of differing textures and to examine the possible factors controlling the trace element distribution in those minerals using LA-ICP-MS spot and line scan analyses. Our results show that there are distinct systematic differences in trace element distributions throughout the different minerals, as follows: (1) pyrite is divided into three types at Kairei, including early-stage euhedral pyrite (py-I), sub-euhedral pyrite (py-II), and colloform pyrite (py-III). Pyrite is generally enriched with Mo, Au, As, Tl, Mn, and U. Pyrite-I has high contents of Se, Te, Bi, and Ni when compared to the other types; py-II is enriched in Au relative to py-I and py-III, but poor in Ni; py-III is enriched in Mo, Pb, and U but is poor in Se, Te, Bi, and Au relative to py-I and py-II. Variations in the concentrations of Se, Te, and Bi in pyrite are most likely governed by the strong temperature gradient. There is generally a lower concentration of nickel than Co in pyrite, indicating that our samples precipitated at high temperatures, whereas the extreme Co enrichment is likely from a magmatic heat source combined with an influence of serpentinization reactions. (2) Chalcopyrite is characterized by high concentrations of Co, Se, and Te. The abundance of Se and Te in chalcopyrite over the other minerals is interpreted to have been caused by the high solubilities of Se and Te in the chalcopyrite lattice at high temperatures. The concentrations of Sb, As, and Au are relatively low in chalcopyrite from the Kairei vent field. (3) Sphalerite from Zn-rich chimneys is characterized by high concentrations of Sn, Co, Ga, Ge, Ag, Pb, Sb, As, and Cd, but is depleted in Se, Te, Bi, Mo, Au, Ni, Tl, Mn, Ba, V, and U in comparison with the other minerals. The high concentrations of Cd and Co are likely caused by the substitution of Cd²⁺ and Co²⁺ for Zn²⁺ in sphalerite. A high concentration of Pb accompanied by a high Ag concentration in sphalerite indicates that Ag occurs as Pb–Ag sulfosalts. Gold is generally low in sphalerite and strongly correlates with Pb, suggesting its presence in microinclusions of galena. The strong correlation of As with Ge in sphalerite from Kairei suggests that they might precipitate at medium temperatures and under moderately reduced conditions. (4) Bornite–digenite has very low concentrations of most trace elements, except for Co, Se, and Bi. Serpentinization in ultramafic-hosted hydrothermal systems might play an important role in Au enrichment in pyrite with low As contents. Compared to felsic-hosted seafloor massive sulfide deposits, sulfide minerals from ultramafic-hosted deposits show higher concentrations of Se and Te, but lower As, Sb, and Au concentrations, the latter often attributed to the contribution of magmatic volatiles. As with typical ultramafic-hosted seafloor massive sulfide deposits, Se enrichment in chalcopyrite from Kairei indicates that the primary factor that controls the Se enrichment is temperature-controlled mobility in vent fluids.

In this paper, we conduct a comparative study on the mineralogy and geochemistry of metalliferous sediment collected near the active hydrothermal site (Wocan-1) and inactive hydrothermal site (Wocan-2) from Wocan Hydrothermal Field, on the Carlsberg Ridge (CR), northwest Indian Ocean. We aim to understand the spatial variations in the primary and post-depositional conditions and the intensity of hydrothermal circulations in the Wocan hydrothermal systems. Sediment samples were collected from six stations which includes TVG-07, TVG-08 (Wocan-1), TVG-05, TVG-10 (Wocan-2), TVG-12 and TVG-13 (ridge flanks). The mineralogical investigations show that sediment samples from Wocan-1 and Wocan-2 are composed of chalcopyrite, pyrite, sphalerite, barite, gypsum, amorphous silica, altered volcanic glass, Fe-oxides, and hydroxides. The ridge flank sediments are dominated by biogenic calcite and foraminifera assemblages. The bulk sediment samples of Wocan-1 have an elevated Fe/Mn ratio (up to ~1545), with lower U contents (<7.4 ppm) and U/Fe ratio (<~1.8 × 10⁻⁵). The sulfide separates (chalcopyrite, pyrite, and sphalerite) are enriched in Se, Co, As, Sb, and Pb. The calculated sphalerite precipitation temperature (Sph.PT) yields ~278 °C. The sulfur isotope (δ³⁴S) analysis returned a light value of 3.0–3.6‰. The bulk sediment samples of Wocan-2 have a lower Fe/Mn ratio (<~523), with high U contents (up to 19.6 ppm) and U/Fe ratio (up to ~6.2 × 10⁻⁵). The sulfide separates are enriched in Zn, Cu, Tl, and Sn. The calculated Sph.PT is ~233 °C. The δ³⁴S returned significant values of 4.1–4.3‰ and 6.4–8.7‰ in stations TVG-10 and TVG-05, respectively. The geochemical signatures (e.g., Fe/Mn and U/Fe ratio, mineral chemistry of sulfides separates, and S-isotopes and Sph.PT) suggest that sediment samples from Wocan-1 are located near intermediate–high temperature hydrothermal discharge environments. Additionally, relatively low δ³⁴S values exhibit a lower proportion (less than 20%) of seawater-derived components. The geochemical signatures suggest that sediment samples from Wocan-2 has undergone moderate–extensive oxidation and secondary alterations by seawater in a low–intermediate temperature hydrothermal environments. Additionally, the significant δ³⁴S values of station TVG-05 exhibit a higher estimated proportion (up to 41%) of seawater-derived components. Our results showed pervasive hydrothermal contributions into station TVG-08 relative to TVG-07, it further showed the increased process of seafloor weathering at TVG-05 relative to TVG-10.

We have studied morphology, mineralogy and geochemical characteristics of Fe-oxyhydroxide deposits from metal-enriched sediments of the active (Wocan-1) and inactive (Wocan-2) hydrothermal sites (Carlsberg Ridge, Northwest Indian Ocean). Fe-oxyhydroxide deposits on the Wocan-1 site are reddish-brownish, amorphous and subangular. They occur in association with sulfides (e.g., pyrite, chalcopyrite and sphalerite) and sulfate minerals (e.g., gypsum and barite). The geochemical composition shows enrichment in transition metals (Ʃ (Cu + Co + Zn + Ni) = ~1.19 wt. %) and low (<0.4 wt. %) values of Al/(Al + Fe + Mn) ratio. The Wocan-2 samples show poorly crystallized reddish brown and yellowish Fe-oxyhydroxide, with minor peaks of goethite and manganese oxide minerals. The mineral assemblage includes sulfide and sulfate phases. The geochemical compositions show two distinct types (type-1 and type-2). The type-1 Fe-oxyhydroxides are enriched in transition metals (up to ~1.23 wt. %), with low values of Fe/Ti vs. Al/(Al + Fe + Mn) ratio similar to the Wocan-1 Fe-oxyhydroxides. The type-2 Fe-oxyhydroxides are depleted in transition metals, with Al/(Al + Fe + Mn) ratio of 0.003–0.58 (mean value, 0.04). The ridge flank oxyhydroxides exhibit an extremely low (mean value ~ 0.01) Fe/Mn ratio and a depleted concentration of transition metals. Our results revealed that the Wocan-1 Fe-oxyhydroxides and type-1 Fe-oxyhydroxides of the Wocan-2 site are in the range of Fe-oxyhydroxides deposits that are precipitated by mass wasting and corrosion of pre-existing sulfides. The type-2 Fe-oxyhydroxides are precipitated from sulfide alteration by seawater in an oxygenated environment relative to type-1. The association of biogenic detritus with the oxyhydroxides of the ridge flanks and the low Fe/Mn ratio suggests hydrogenous/biogenic processes of formation and masked hydrothermal signatures with distance away from the Wocan hydrothermal field.

Hydrothermal activity on mid‐ocean ridges plays an important role in shaping marine chemistry, yet the variability of hydrothermal venting and its forcing mechanism remain elusive. Here, we analyzed a sediment core obtained near the tectonic‐controlled Tianxiu vent field, Carlsberg Ridge, to reconstruct the hydrothermal venting history. The core documented two significant hydrothermal events (H1 and H2) in the past 30 ka. H1 occurred at 24.1–24.5 ka during the Last Glacial Maximum (LGM), while H2 occurred at 10.5–11.6 ka during the deglacial period. Compared to H2, H1 was relatively weak, and it occurred concurrently with a tectonic event. We suggest that H2 was caused by the increased melt production associated with the decompression melting of the upper mantle during sea‐level fall, which is consistent with previously published records, whereas H1 was likely triggered by an intense tectonic event associated with depressurization during the LGM, which was previously unrecognized.

One gravity core retrieved from the Niger Delta was used to explore the origin of deposited organic matter (OM) and the paleo-climatic and environmental conditions over the Holocene in equatorial West Africa. The geochemical properties of sediments including glycerol dialkyl glycerol tetraethers (GDGTs) and elemental (%OC, %N, C/N) and isotopic (δ¹³C_org, δ¹⁵N) signatures were determined. The determination constrained the age of the column and revealed that the sediment OM was mainly derived from a marine source. The isoprenoid (iso)GDGTs were the dominant GDGTs, with a small amount of branched (br)GDGTs, which led to a low-branched and isoprenoid tetraether index (BIT, 0.02–0.21) and represented a low terrestrial input. Most isoGDGTs and OH-GDGTs were produced in situ by Marine Group I (MG-I) Thaumarchaeota, while the brGDGTs were mainly transported from land. A two-endmember model quantified the contribution of terrestrial OM, as 0.9–19.9% by BIT and 1.1–32.6% by δ¹³C. Accordingly, the millennium-scale sea surface temperatures (SSTs) were reconstructed based on the cyclopentane ring distribution (${\mathrm{T}\mathrm{E}\mathrm{X}}_{86}^{\mathrm{H}}$) and the ring index of OH-GDGTs (RI-OH). The top core SSTs were lower than the modern mean annual SST due to the growth season and habitat depth of Thaumarchaeota. The reconstructed SSTs clearly revealed the four stages of paleoclimate change, in particular, the drought episode of 8.2 kyr and the following humid period. The above research has enhanced our understanding of the paleoclimate change in river outflow during the Holocene at the millennium scale.