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Granitic gneiss (orthogneiss) and Himalayan leucogranite are widely distributed in the Himalayan orogen, but whether or not the granitic gneiss made a contribution to the Himalayan leucogranite remains unclear. In this study, we present the petrological, geochronological and geochemical results for orthogneisses and leucogranites from the Zhada area, Western Himalayas. Zhada orthogneiss is composed mainly of quartz, plagioclase, K‐feldspar, biotite and muscovite, with accessory zircon and apatite. Orthogneiss zircon cathodoluminescence (CL) images show that most grains contain a core with oscillatory zoning, which indicates an igneous origin. Sensitive high‐resolution ion microprobe (SHRIMP) U‐Pb dating of the zircon cores in the orthogneiss shows a weighted 206Pb/238U age of 515 ± 4 Ma (early Paleozoic), with spongelike zircon rims of 17.9 ± 0.5 Ma (Miocene). Zhada leucogranite shows 206Pb/238U ages ranging from 19.0 ± 0.4 Ma to 12.4 ± 0.2 Ma, the weighted average age being 16.2 ± 0.4 Ma. The leucogranites have a low Ca content (<1 wt%), FeOt content (<1 wt%), Rb content (67.0–402 ppm), Sr content (<56.6 ppm), Ba content (3.35–238 ppm) and Rb/Sr ratio (0.5–14.7), which are similar to the geochemical characteristics of the Himalayan leucogranite derived from muscovite dehydration partial melting of metasediments and representative of most Himalayan leucogranites. The highly variable Na2O + K2O (4.33 wt%–9.13 wt%), Al2O3 (8.44 wt%–13.51 wt%), ∑REE (40.2–191.0 ppm), Rb (67.0–402 ppm) and Nb (8.23–26.4 ppm) contents, 87Sr/86Sr(t) ratios (0.7445–0.8605) and εNd(t) values (–3.6 to –8.2) indicate that the leucogranite is derived from a heterogenetic source. The nonradiogenic Nd isotope values of the studied Zhada leucogranite and orthogneiss range from –8.2 to –3.6 and from –8.7 to –4.1, respectively. Therefore, the general mixing equation was used to perform the Sr and Nd isotope mixing calculations. The results indicate that the heterogenetic source was the Tethyan Himalayan Sequence (THS)/Higher Himalayan Crystalline (HHC) metasediments and Zhada orthogneiss. The Zhada area experienced crustal anatexis during the Miocene and the heterogenetic source of the orthogneiss and metasediment may have experienced crustal anatexis controlled by muscovite dehydration. The Zhada leucogranite inherited not only the geochemical characteristics of the Himalayan metasediment (muscovite dehydration melting), but also the trace elements and Sr‐Nd isotopic characteristics of the Zhada orthogneiss. These results indicate that the Paleozoic Zhada orthogneiss was involved in crustal anatexis at 17.9 ± 0.5 Ma (Miocene) and that the muscovite dehydration of the metasediments in the heterogenetic source produced fluid, which may have caused the orthogneiss solidus lines to decline, triggering a partial melting of the Zhada orthogneiss. It is therefore proposed that Himalayan leucogranite is a crust‐derived granite rather than a S‐type granite, as previously hypothesized.

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The Bayan Obo rare earth element (REE) deposit in Inner Mongolia, northern China, is the largest REE deposit in the world, whose mineralization process remains controversial. There are dozens of carbonatite dykes that are tightly related to the deposit. Here we report the petrological and mineralogical characteristics of a typical dolomite carbonatite dyke near the deposit. The dolomite within the dyke experienced intense post-emplacement fluids metasomatism as evidenced by the widespread hydrothermal REE-bearing minerals occurring along the carbonate mineral grains. REE contents of bulk rocks and constituent dolomite minerals (>90 vol.%) are 1407–4184 ppm and 63–152 ppm, respectively, indicating that dolomite is not the dominant mineral controlling the REE budgets of the dyke. There are three types of apatite in the dyke: Type 1 apatite is the primary apatite and contains REE2O3 at 2.35–4.20 wt.% and SrO at 1.75–2.19 wt.%; Type 2 and Type 3 apatites are the products of replacement of primary apatite. The REE2O3 (6.10–8.21 wt.%) and SrO (2.83–3.63 wt.%) contents of Type 2 apatite are significantly elevated for overprinting of REE and Sr-rich fluids derived from the carbonatite. Conversely, Type 3 apatite has decreased REE2O3 (1.17–2.35 wt.%) and SrO (1.51–1.99 wt.%) contents, resulting from infiltration of fluids with low REE and Na concentrations. Our results on the dyke suggest that post-magmatic fluids expelled from the carbonatitic melts dominated the REE mineralization of the Bayan Obo deposit, and a significant fluid disturbance occurred but probably provided no extra REEs to the deposit.