Jianhui Wu

Jianhui Wu


Research Focus & Metrics

Academic Career Length

1Year (2026-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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13 March 2026 in Minerals
Verified
Journal Article
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ZWZeyu Wang Wang
Zeyu Wang Wang
JWJianhui Wu
Jianhui Wu
XDXiaofang Dou
Xiaofang Dou
GCGen Chen
Gen Chen
JWJiangang Wei
Jiangang Wei
治李治彬 李
治彬 李
With the deepening of deep mineral exploration, traditional methods face bottlenecks in identifying concealed orebodies, making the establishment of a mineralogical exploration indicator system for collision-type porphyry deposits imperative. This study investigates chlorite from the Cimabanshuo Porphyry Copper Deposit in the Zhunuo Ore Concentration Area of the Western Gangdese via systematic petrographic and in situ geochemical analyses, to elucidate the spatial evolution of its trace element compositions and assess the validity and applicability of different trace elements for hydrothermal center indication. Based on micropetrographic observations, chlorite is classified into three types: biotite-altered (Chl-1), amphibole-altered (Chl-2) and vein-type (Chl-3), with Chl-1 and Chl-2 significantly affected by primary mineral compositions. Trace element results show that spatial variations in Ti, Li, Ni, Co, Mn, and Sr contents and Li/Mn and Ti/Sr ratios in chlorite can clearly indicate the mineralization center—Ti, Li, Ni and Co are systematically enriched in the proximal ore zone by temperature and fluid compositional effects, while Mn and Sr are enriched in the distal ore zone due to elemental redistribution during fluid migration. Fitting analysis of chlorite elemental ratios against the distance from sampling points to the mineralization center indicates the Li/Mn ratio decreases with increasing distance (R2 = 0.4665), consistent with elemental distribution and showing a certain correlation; in contrast, the Ti/Sr ratio has a fitting coefficient of determination of only 0.0581, which cannot serve as an effective analysis indicator for this study because the deposit’s plate collision metallogenic setting causes elemental migration to be disturbed by local geological factors. In addition, chlorite in the zones 0–500 m from the Cu I, Cu II, and Cu III orebodies and 1–1.5 km to the north is characterized by significant enrichment of Ti, Li, Ni, and Co, depletion of Mn and Sr and high Li/Mn ratios. Accordingly, a concealed hydrothermal center is inferred in the northern part of the Cimabanshuo Deposit beyond the proven orebodies. Comprehensive studies confirm that the spatial variation characteristics of trace elements in chlorite from the Cimabanshuo Porphyry Copper Deposit have high applicability for indicating hydrothermal mineralization centers.

20 February 2026 in Minerals
Verified
Journal Article
Open access
PDF file
LGLi Qing Gong
Li Qing Gong
ZSZhang Jin Shu
Zhang Jin Shu
JWJianhui Wu
Jianhui Wu
Xiaojia JiangXiaojia Jiang
Xiaojia Jiang
BPBei Pang
Bei Pang
The Zhunuo ore district, at the western end of the Gangdese porphyry Cu belt, hosts significant Cu mineralization and newly recognized W mineralization dominated by scheelite. However, the genetic relationship between scheelite and porphyry mineralization, and the evolution of ore-forming fluids remain poorly constrained. To address this, scheelite samples from multiple locations were analyzed for major elements (EMPA), in situ trace elements (LA-ICP-MS), and internal textures (cathodoluminescence, CL). These data, combined with machine learning methods, were used to determine scheelite genetic types and reconstruct fluid evolution. REE patterns and CL textures reveal three scheelite generations in Yalongri (early Sch I c, middle Sch I b, late Sch I a), two in Zhigunong (early Sch II a, late Sch II b), and one in Xiongbaxi (Sch III). Low Na (0–329 ppm) and Nb (3.9–39 ppm) relative to high ΣREE + Y-Eu (16–3857 ppm), indicate that the dominant substitution mechanism is 3Ca2+ = 2REE3+ + □Ca (□Ca = Ca vacancy). δEu values > 1 in Sch I a, Sch I b, Sch II a, and Sch II b indicate reducing fluids, whereas δEu < in Sch I c and Sch III reflects oxidizing conditions. Variations in REE, Mo, and Sr contents suggest that ore-forming fluids in Yalongri evolved from oxidizing to reducing conditions, with late-stage scheelite undergoing dissolution–reprecipitation. Zhigunong records two reducing stages: an early REE-rich-Mo-poor stage and a later REE-poor-Mo-rich stage. Xiongbaxi records a single oxidizing, REE-rich, Mo-rich stage. Scheelite exhibits low-to-moderate Sr/Mo ratios (0.02–6.10), consistent with a magmatic–hydrothermal origin, and relatively uniform Y/Ho ratios (12–59) indicating stable crystallization conditions. A Random Forest model classifies scheelite into orogenic, porphyry, skarn, and greisen types. Overall, the results indicate that ore-forming fluids evolved from oxidizing to reducing conditions, favoring metal transport and enrichment. Integrated geochemical and machine learning evidence suggest, strong potential for porphyry-type Cu-W(-Mo) mineralization in Yalongri and Zhigunong, and skarn-type W-Mo mineralization in Xiongbaxi, providing important guidance for future exploration in the western Gangdese metallogenic belt.