Fluorine and chlorine in mantle minerals and the halogen budget of the Earth’s mantle

The fluorine (F) and chlorine (Cl) contents of arc magmas have been used to track the composition of subducted components, and the F and Cl contents of MORB have been used to estimate the halogen content of depleted MORB mantle (DMM). Yet, the F and Cl budget of the Earth’s upper mantle and their distribution in peridotite minerals remain to be constrained. Here, we developed a method to measure low concentrations of halogens (≥0.4 µg/g F and ≥0.3 µg/g Cl) in minerals by secondary ion mass spectroscopy. We present a comprehensive study of F and Cl in co-existing natural olivine, orthopyroxene, clinopyroxene, and amphibole in seventeen samples from different tectonic settings. We support the hypothesis that F in olivine is controlled by melt polymerization, and that F in pyroxene is controlled by their Na and Al contents, with some effect of melt polymerization. We infer that Cl compatibility ranks as follows: amphibole > clinopyroxene > olivine ~ orthopyroxene, while F compatibility ranks as follows: amphibole > clinopyroxene > orthopyroxene ≥ olivine, depending on the tectonic context. In addition, we show that F, Cl, Be and B are correlated in pyroxenes and amphibole. F and Cl variations suggest that interaction with slab melts and fluids can significantly alter the halogen content of mantle minerals. In particular, F in oceanic peridotites is mostly hosted in pyroxenes, and proportionally increases in olivine in subduction-related peridotites. The mantle wedge is likely enriched in F compared to un-metasomatized mantle, while Cl is always low (<1 µg/g) in all tectonic settings studied here. The bulk anhydrous peridotite mantle contains 1.4–31 µg/g F and 0.14–0.38 µg/g Cl. The bulk F content of oceanic-like peridotites (2.1–9.4 µg/g) is lower than DMM estimates, consistent with F-rich eclogite in the source of MORB. Furthermore, the bulk Cl budget of all anhydrous peridotites studied here is lower than previous DMM estimates. Our results indicate that nearly all MORB may be somewhat contaminated by seawater-rich material and that the Cl content of DMM could be overestimated. With this study, we demonstrate that the halogen contents of natural peridotite minerals are a unique tool to understand the cycling of halogens, from ridge settings to subduction zones.     

Noble-metal ore genesis and mantle–crust interaction

The mineral and geochemical compositions of noble-metal (first of all, gold) deposits of the Fennoscandian, Siberian, and Northeast Asian orogenic belts are considered. These deposits are of several types: Au (disseminated Au–sulfide and Au–quartz), Au–Bi, Au–Ag, Au–Sb, Ag–Sb, Au–Sb–Hg, and Ag–Hg. They formed in different geodynamic settings as a result of the active motion of crustal tectonic blocks of different nature. Subduction processes (both at the front and at the rear of continent-marginal and island-arc magmatic arcs) resulted in Au–Ag, Ag–Sb, Ag–Hg, Au–Sb–Hg, and Au–Bi deposits. Collision events gave rise to Au and Au–Bi deposits. Intraplate continental rifting and formation of orogenic belts along the boundaries of block (plate) sliding led to the origin of Au and Au–Bi ores in association with Au–Ag, Au–Sb–Hg, and complex ores. In all cases, the formation of noble-metal mineralization was accompanied by magmatism of different types and metamorphism. Because of this diversity of ores, there is no single concept of the genesis of noble-metal mineralization. Several competing models of genesis exist: hydrothermal-metamorphic, pluton-metamorphic, plutonic, activity of mantle fluid flows, and multistage concentration during the crust–mantle interaction with the leading role of sedimentary complexes.     

Hydration and dehydration in the lower margin of a cold mantle wedge: implications for crust–mantle interactions and petrogeneses of arc magmas

Garnet orthopyroxenites from Maowu (Dabieshan orogen, eastern China) were formed from a refractory harzburgite/dunite protolith. They preserve mineralogical and geochemical evidence of hydration/metasomatism and dehydration at the lower edge of a cold mantle wedge. Abundant polyphase inclusions in the cores of garnet porphyroblasts record the earliest metamorphism and metasomatism in garnet orthopyroxenites. They are mainly composed of pargasitic amphibole, gedrite, chlorite, talc, phlogopite, and Cl-apatite, with minor anhydrous minerals such as orthopyroxene, sapphirine, spinel, and rutile. Most of these phases have high X_Mg, NiO, and Ni/Mg values, implying that they probably inherited the chemistry of pre-existing olivine. Trace element analyses indicate that polyphase inclusions are enriched in large ion lithophile elements (LILE), light rare earth elements (LREE), and high field strength elements (HFSE), with spikes of Ba, Pb, U, and high U/Th. Based on the P–T conditions of formation for the polyphase inclusions (?1.4 GPa, 720–850°C), we suggest that the protolith likely underwent significant hydration/metasomatism by slab-derived fluid under shallow–wet–cold mantle wedge corner conditions beneath the forearc. When the hydrated rocks were subducted into a deep–cold mantle wedge zone and underwent high-pressure–ultrahigh-pressure (HP–UHP) metamorphism, amphibole, talc, and chlorite dehydrated and garnet, orthopyroxene, Ti-chondrodite, and Ti-clinohumite formed during prograde metamorphism. The majority of LILE (e.g. Ba, U, Pb, Sr, and Th) and LREE were released into the fluid formed by dehydration reactions, whereas HFSE (e.g. Ti, Nb, and Ta) remained in the cold mantle wedge lower margin. Such fluid resembling the trace element characteristics of arc magmas evidently migrates into the overlying, internal, hotter part of the mantle wedge, thus resulting in a high degree of partial melting and the formation of arc magmas.     

Characteristics of mantle branch structure in western Shandong and its roles in minerogenesis and ore-controlling

1 The rise of the problem The region of western Shandong has been attracting more and more attention of geologists because of its unique geological features and abundant mineral resources, and it has been well geologically documented (Lin Jingqian et al.…     

Time series analysis of mantle cycles Part Ⅱ:The geologic record in zircons,large igneous provinces and mantle lithosphere

Igneous and detrital zircons have six major U/Pb isotopic age peaks in common(2700 Ma,1875 Ma.1045 Ma,625 Ma,265 Ma and 90 Ma).For igneous rocks,each age peak is comprised of subpeaks with distinct geographic distributions and a subpeak age range per age peak ≤100 Myr.There are eight major LIP age peaks(found on≥10 crustal provinces)of which only four are in common to major detrital zircon age peaks(2715 Ma,1875 Ma,825 Ma,90 Ma).Of the whole-rock Re depletion ages,58% have correspo nding detrital zircon age peaks and 55% have corresponding LIP age peaks.Ten age pea ks are fou nd in common to igneous zircon,detrital zircon,LIP,and Re depletion age time series(3225 Ma,2875 Ma,2145 Ma,2085 Ma,1985 Ma,1785 Ma,1455 Ma,1175 Ma,825 Ma,and 90 Ma).and these are very robust peaks on a global scale as recorded in both crustal and mantle rocks.About 50% of the age peaks in each of these time series correspond to predicted peaks in a 94-Myr mantle cycle,including four of the ten peaks in common to all four time series(2875 Ma,1785 Ma,825 Ma and 90 Ma).Age peak widths and subpeak ranges per age peak suggest that mantle events responsible for age peaks are100 Myr and many50 Myr in duration.Age peak geographic distributions show three populations(≤1000 Ma,2500-1000 Ma,2500 Ma),with the number of new provinces in which age peaks are represented decreasing with time within each population.The breaks between the populations(at 2.5 Ga and 1 Ga)fall near the onsets of two transitions in Earth history.The First Transition may represent a change from stagnant-lid tectonics into plate tectonics and the Second Transition,the onset of subduction of continental crust.The major factor controlling geographic distribution of age peaks is the changing locations of orogeny.Before ～2 Ga,age subpeaks and peaks are housed in orogens within or around the edges of crustal provinces,mostly in accretionary orogens.but beginning at 1.9 Ga,collisional orogens become more important.The coincidence in duration between magmatic flare-ups in Phanerozoic arcs and duration of age subpeaks(10-30 Myr)is consiste nt with subpeaks representing periods of enhanced arcrelated magmatism.probably caused by increased subduction flux.The correlation of isotopic age peaks between time series supports a cause and effect relationship between mantle plume activity,continental magma production at convergent margins,and crustal deformation.Correlation of over half of the detrital zircon age peaks(and six of the nine major peaks)with Re depletion age peaks supports an interpretation of the zircon peaks as crustal growth rather than selective preservation peaks.     

An experimental study of Fe–Ni exchange between sulfide melt and olivine at upper mantle conditions: implications for mantle sulfide compositions and phase equilibria

The behavior of nickel in the Earth’s mantle is controlled by sulfide melt–olivine reaction. Prior to this study, experiments were carried out at low pressures with narrow range of Ni/Fe in sulfide melt. As the mantle becomes more reduced with depth, experiments at comparable conditions provide an assessment of the effect of pressure at low-oxygen fugacity conditions. In this study, we constrain the Fe–Ni composition of molten sulfide in the Earth’s upper mantle via sulfide melt–olivine reaction experiments at 2 GPa, 1200 and 1400 °C, with sulfide melt \(X_{{{\text{Ni}}}}^{{{\text{Sulfide}}}}=\frac{{{\text{Ni}}}}{{{\text{Ni}}+{\text{Fe}}}}\) (atomic ratio) ranging from 0 to 0.94. To verify the approach to equilibrium and to explore the effect of \({f_{{{\text{O}}_{\text{2}}}}}\) on Fe–Ni exchange between phases, four different suites of experiments were conducted, varying in their experimental geometry and initial composition. Effects of Ni secondary fluorescence on olivine analyses were corrected using the PENELOPE algorithm (Baró et al., Nucl Instrum Methods Phys Res B 100:31–46, 1995), “zero time” experiments, and measurements before and after dissolution of surrounding sulfides. Oxygen fugacities in the experiments, estimated from the measured O contents of sulfide melts and from the compositions of coexisting olivines, were 3.0?±?1.0 log units more reduced than the fayalite–magnetite-quartz (FMQ) buffer (suite 1, 2 and 3), and FMQ ??1 or more oxidized (suite 4). For the reduced (suites 1–3) experiments, Fe–Ni distribution coefficients \(K_{{\text{D}}}^{{}}=\frac{{(X_{{{\text{Ni}}}}^{{{\text{sulfide}}}}/X_{{{\text{Fe}}}}^{{{\text{sulfide}}}})}}{{(X_{{{\text{Ni}}}}^{{{\text{olivine}}}}/X_{{{\text{Fe}}}}^{{{\text{olivine}}}})}}\) are small, averaging 10.0?±?5.7, with little variation as a function of total Ni content. More oxidized experiments (suite 4) give larger values of K_D (21.1–25.2). Compared to previous determinations at 100 kPa, values of K_D from this study are chiefly lower, in large part owing to the more reduced conditions of the experiments. The observed difference does not seem attributable to differences in temperature and pressure between experimental studies. It may be related in part to the effects of metal/sulfur ratio in sulfide melt. Application of these results to the composition of molten sulfide in peridotite indicates that compositions are intermediate in composition (\(X_{{{\text{Ni}}}}^{{{\text{sulfide}}}}\)?~?0.4–0.6) in the shallow mantle at 50 km, becomes more Ni rich with depth as the O content of the melt diminishes, reaching a maximum (0.6–0.7) at depths near 80–120 km, and then becomes more Fe rich in the deeper mantle where conditions are more reduced, approaching (\(X_{{{\text{Ni}}}}^{{{\text{sulfide}}}}\)?~?0.28)?>?140 km depth. Because Ni-rich sulfide in the shallow upper mantle melts at lower temperature than more Fe-rich compositions, mantle sulfide is likely molten in much of the deep continental lithosphere, including regions of diamond formation.     

Fe–Mg partitioning between post-perovskite and ferropericlase in the lowermost mantle

Fe–Mg partitioning between post-perovskite and ferropericlase has been studied using a laser-heated diamond anvil cell at pressures up to 154 GPa and 2,010 K which corresponds to the conditions in the lowermost mantle. The composition of the phases in the recovered samples was determined using analytical transmission electron microscopy. Our results reveal that the Fe–Mg partition coefficient between post-perovskite and ferropericlase (K _D^PPv/Fp) increases with decreasing bulk iron content. The compositional dependence of K _D^PPv/Fp on the bulk iron content explains the inconsistency in previous studies, and the effect of the bulk iron content is the most dominant factor compared to other factors, such as temperature and aluminum content. Iron prefers ferropericlase compared to post-perovskite over a wide compositional range, whereas the iron content of post-perovskite (X _Fe^PPv, the mole fraction) does not exceed a value of 0.10. The iron-rich ferropericlase phase may have significant influence on the physical properties, such as the seismic velocity and electrical conductivity at the core–mantle boundary region.     

Mantle dynamics and mantle melting beneath Niuafo’ou Island and the northern Lau back-arc basin

A suite of young volcanic basaltic lavas erupted on the intra-plate island of Niuafo’ou and at active rifts and spreading centres (the King’s Triple Junction and the Northeastern Lau Spreading Centre) in the northern Lau Basin is used to examine the pattern of mantle flow and the dynamics of melting beneath this complex back-arc system. All lavas contain variable amounts of a subduction related component inherited from the Tonga subduction zone to the east. All lavas have higher ⁸⁷Sr/⁸⁶Sr, lower ¹⁴³Nd/¹⁴⁴Nd and more radiogenic Pb isotope compositions than basalts erupted at the Central Lau Spreading Centre in the central Lau Basin, and are interpreted as variable mixtures of subduction-modified, depleted upper mantle, and mantle residues derived from melting beneath the Samoan Islands which has leaked through a tear in the subducting Pacific Plate beneath the Vitiaz Lineament at the northern edge of the Lau Basin. Our data can be used to map out the present-day distribution of Samoan mantle in this region, and show that it influences the compositions of lavas erupted as far as 400 km from the Samoan Islands. The distribution of Samoan-influenced lavas implies south- and southwest-wards mantle flow rates of >4 cm/year. U-series disequilibria in historic Niuafo’ou lavas have average (²³⁰Th/²³⁸U) = 1.13, (²³¹Pa/²³⁵U) = 2.17, (²²⁶Ra/²³⁰Th) = 2.11, and together with major and trace element data require ∼5% partial melting of mantle at between 2 and 3 GPa, with a residual porosity of 0.002 and an upwelling rate of 1 cm year⁻¹. We suggest that intraplate magmatism in the northern Lau Basin results from decompression melting during southward flow of mantle from beneath old (110–120 Ma), relatively thick Pacific oceanic lithosphere to beneath young (<5 Ma), thinner oceanic lithosphere beneath the northern Lau Basin.     

Evolution and composition of the lithospheric mantle underneath the western Arabian peninsula: constraints from Sr−Nd isotope systematics of mantle xenoliths

On the basis of their textures and mineral compositions spinel-peridotite xenoliths of the Cr-diopside group (group I) from Cenozoic volcanic fields of Arabia can be classified into different subtypes. Type IA is of lherzolitic to harzburgitic composition; mineral compositions are similar to those of group I mantle xenoliths from worldwide occurrences. Type IB xenoliths have lherzolitic to wehrlitic compositions; Mg/(Mg+Fe) ratios of the clinopyroxenes (0.862–0.916) and olivines (0.872–0.914) are similar too or slightly lower than those of typical IA minerals. Texturally, type IB xenoliths are distinguished from type IA rocks by the presence of intragranular spinel, intragranular relict Cr-pargasite, and subordinate intergranular Ba-phlogopite (11.1% BaO). The hydrous minerals in type IB xenoliths are interpreted to document an earlier metasomatism 1 which did not affect type IA lithospheric mantle. Subsequent recrystallization caused the partial replacement of Cr-pargasite in type IB materials and resulted in the formation of less hydrous mineral assemblages. Some of the type IA xenoliths are characterized by secondary intergranular amphibole which must have formed recently. The absence or presence of this intergranular amphibole is used to distinguish an anhydrous subtype IA1 from a hydrous subtype IA2. Type IB xenoliths may also contain secondary intergranular amphibole (similar to the one in subtype IA2) or they contain abundant formermelt patches now consisting of glass and phenocrysts of olivine, clinopyroxene, amphibole, and spinel. The secondary intergranular amphiboles and the former melt patches, both are interpreted as results of a second metasomatism (metasomatism 2). In their trace element and isotopic characteristics, type IA1 and type IA2 clinopyroxenes do not exhibit any systematic differences. Furthermore, type IA2 clinopyroxenes are in Sr isotopic disequilibrium with intergranular amphiboles. This suggests that type IA2 clinopyroxenes were not modified during the second metasomatism 2. All type IA clinopyroxenes have low Sr contents (100 ppm); most of them show Sm/Nd ratios higher than inferred for bulk earth. In their ⁸⁷Sr/⁸⁶Sr and ¹⁴³Nd/¹⁴⁴Nd ratios, type IA clinopyroxenes exhibit a large spread from 0.70226–0.70376 and from 0.51375–0.51251, respectively. Highly variable Sr/Nd ratios (5.0–79.3) and variable T_UR and T_CHUR model age relationships require different evolutions of the respective mantle portions. Nevertheless, all but two type IA clinopyroxenes form a linear array in a Sm–Nd isochron diagram which probably can not be explained by mixing. If taken as an isochron the slope of the array corresponds to an age of around 700 Ma. The mean initial _Nd of 5.8±1.7 (1) is similar to values for juvenile Pan-African (i.e. 850–650 Ma old) crust of the Arabian-Nubian shield. It is suggested that type IA lithospheric mantle and the juvenile Pan-African crust are two counterparts fractionated from a common source during the earlier stages of the Pan-African. Type IB clinopyroxenes have high Sr contents (200 ppm), variable Sr/Nd ratios (9–111) and Sm/Nd ratios generally below that inferred for bulk earth, and show a small spread in their Sr and Nd isotopic compositions (0.70299–0.70318 and 0.51285–0.51278, respectively). In a Sm–Nd isochron diagram the data points form a linear, horizontal array indicating a close-to-zero age for the earlier metasomatism 1 and suggesting a close genetic relationship to mantle processes related to the formation of the Red Sea.     

Evolution of subcontinental lithospheric mantle beneath eastern China: Re–Os isotopic evidence from mantle xenoliths in Paleozoic kimberlites and Mesozoic basalts

The ages of subcontinental lithospheric mantle beneath the North China and South China cratons are less well-constrained than the overlying crust. We report Re–Os isotope systematics of mantle xenoliths entrained in Paleozoic kimberlites and Mesozoic basalts from eastern China. Peridotite xenoliths from the Fuxian and Mengyin Paleozoic diamondiferous kimberlites in the North China Craton give Archean Re depletion ages of 2.6–3.2 Ga and melt depletion ages of 2.9–3.4 Ga. No obvious differences in Re and Os abundances, Os isotopic ratios and model ages are observed between spinel-facies and garnet-facies peridotites from both kimberlite localities. The Re–Os isotopic data, together with the PGE concentrations, demonstrate that beneath the Archean continental crust of the eastern North China Craton, Archean lithospheric mantle of spinel- to diamond-facies existed without apparent compositional stratification during the Paleozoic. The Mesozoic and Cenozoic basalt-borne peridotite and pyroxenite xenoliths, on the other hand, show geochemical features indicating metasomatic enrichment, along with a large range of the Re–Os isotopic model ages from Proterozoic to Phanerozoic. These features indicate that lithospheric transformation or refertilization through melt-peridotite interaction could be the primary mechanism for compositional changes during the Phanerozoic, rather than delamination or thermal-mechanical erosion, despite the potential of these latter processes to play an important role for the loss of garnet-facies mantle. A fresh garnet lherzolite xenolith from the Yangtze Block has a Re depletion age of ∼1.04 Ga, much younger than overlying Archean crustal rocks but the same Re depletion ages as spinel lherzolite xenoliths from adjacent Mesozoic basalts, indicating Neoproterozoic resetting of the Re–Os system in the South China Craton.     

Telecommunication interactions between microplates and basal mantle LLSVPs.SCIEI北大核心CSCD

基于海洋地质地球物理观测建立的板块构造理论意味着板块和浅部地幔共同演化,然而地幔底部尤其是大型横波低速异常区(LLSVP)与板块(尤其微板块)运动和演化之间是否存在关联仍有争议。一些研究认为LLSVP长期保持稳定,而另一些模型则认为它与各级板块存在相互作用。为此,本文通过总结前人成果,并基于近期发表的板块重建和地幔对流模型进行进一步分析,探讨微板块运动和LLSVP的演化关系。模拟结果表明,微板块与大板块类似,俯冲后通常会下沉至核幔边界。微幔块会推动地幔底部热的物质聚集并形成大的热化学结构。该热化学结构与层析成像揭示的LLSVP基本吻合。下地幔径向流速场和温度场的二阶结构与地表速度场散度的二阶结构随时间的移动轨迹相似,表明深浅部圈层的耦合演化,但是下地幔结构演化一般会滞后于浅表。在微幔块推挤之下,地幔柱优先沿着地幔底部热化学结构的边缘形成,且有时会被推至热化学结构的内部。地幔柱上升至浅部后,能够导致岩石圈弱化甚至裂解或板块边界跃迁,形成微板块。因此,地幔底部LLSVP不是稳定或静止的,而是与微板块动态协同演化,并通过地幔柱与浅表板块边界发生遥相关,从而控制微板块生成场所。     

Partial melting of secondary pyroxenite at 1 and 1.5 GPa,and its role in upwelling heterogeneous mantle

We performed partial melting experiments at 1 and 1.5 GPa, and 1180–1400 °C, to investigate the melting under mantle conditions of an olivine-websterite (GV10), which represents a natural proxy of secondary (or stage 2) pyroxenite. Its subsolidus mineralogy consists of clinopyroxene, orthopyroxene, olivine and spinel (+garnet at 1.5 GPa). Solidus temperature is located between 1180 and 1200 °C at 1 GPa, and between 1230 and 1250 °C at 1.5 GPa. Orthopyroxene (±garnet), spinel and clinopyroxene are progressively consumed by melting reactions to produce olivine and melt. High coefficient of orthopyroxene in the melting reaction results in relatively high SiO₂ content of low melt fractions. After orthopyroxene exhaustion, melt composition is controlled by the composition of coexisting clinopyroxene. At increasing melt fraction, CaO content of melt increases, whereas Na₂O, Al₂O₃ and TiO₂ behave as incompatible elements. Low Na₂O contents reflect high partition coefficient of Na between clinopyroxene and melt (\(D_{{{\text{Na}}_{ 2} {\text{O}}}}^{{{\text{cpx}}/{\text{liquid}}}}\)). Melting of GV10 produces Quartz- to Hyperstene-normative basaltic melts that differ from peridotitic melts only in terms of lower Na₂O and higher CaO contents. We model the partial melting of mantle sources made of different mixing of secondary pyroxenite and fertile lherzolite in the context of adiabatic oceanic mantle upwelling. At low potential temperatures (T _P < 1310 °C), low-degree melt fractions from secondary pyroxenite react with surrounding peridotite producing orthopyroxene-rich reaction zones (or refertilized peridotite) and refractory clinopyroxene-rich residues. At higher T _P (1310–1430 °C), simultaneous melting of pyroxenite and peridotite produces mixed melts with major element compositions matching those of primitive MORBs. This reinforces the notion that secondary pyroxenite may be potential hidden components in MORB mantle source.     

Lithospheric structure and crust–mantle decoupling in the southeast edge of the Tibetan Plateau

Convergence between the Indian plate and the Eurasian plate has resulted in the uplift of the Tibetan Plateau, and understanding the associated dynamical processes requires investigation of the structures of the crust and the lithosphere of the Tibetan Plateau. Yunnan is located in the southwest edge of the plateau and adjacent to Myanmar to the west. Previous observations have confirmed that there is a sharp transition in mantle anisotropy in this area, as well as clockwise rotations of the surface velocity, surface strain, and fault orientation. We use S receiver functions from 54 permanent broad-band stations to investigate the structures of the crust and the lithosphere beneath Yunnan. The depth of the Moho is found to range from 36 to 40 km beneath southern Yunnan and from 55 to 60 km beneath northwestern Yunnan, with a dramatic variation across latitude 25–26°N. The depth of the lithosphere–asthenosphere boundary (LAB) ranges from 180 km to less than 70 km, also varying abruptly across latitude 25–26°N, which is consistent with the sudden change of the fast S-wave direction (from NW–SE to E–W across 26–28°N). In the north of the transition belt, the lithosphere is driven by asthenospheric flow from Tibet, and the crust and the upper mantle are mechanically coupled and moving southward. Because the northeastward movement of the crust in the Burma micro-plate is absorbed by the right-lateral Sagaing Fault, the crust in Yunnan keeps the original southward movement. However, in the south of the transition belt, the northeastward mantle flow from Myanmar and the southward mantle flow from Tibet interact and evolve into an eastward flow (by momentum conservation) as shown by the structure of the LAB. This resulting mantle flow has a direction different from that of the crustal movement. It is concluded that the Sagaing Fault causes the west boundary condition of the crust to be different from that of the lithospheric mantle, thus leading to crust–mantle decoupling in Yunnan.