High-pressure granulites: formation, recovery of peak conditions and implications for tectonics

High‐pressure granulites are characterised by the key associations garnet‐clinopyroxene‐plagioclase‐quartz (in basic rocks) and kyanite‐K‐feldspar (metapelites and felsic rocks) and are typically orthopyroxene‐free in both basic and felsic bulk compositions. In regional metamorphic areas, two essential varieties exist: a high‐ to ultrahigh‐temperature group and a group representing overprinted eclogites. The high‐ to ultrahigh‐temperature type formerly contained high‐temperature ternary feldspar (now mesoperthite) coexisting with kyanite, is associated with garnet peridotites, and formed at conditions above 900 °C and 1.5 GPa. Clinopyroxene in subordinate basic rocks is Al‐rich and textural evidence points to a high‐pressure–high‐temperature melting history. The second variety contains symplectite‐like or poikilitic clinopyroxene‐plagioclase intergrowths indicating former plagioclase‐free, i.e. eclogite facies assemblages. This type of rock formed at conditions straddling the high‐pressure amphibolite/high‐pressure granulite field at around 700–850 °C, 1.0–1.4 GPa. Importantly, in the majority of high‐pressure granulites, orthopyroxene is secondary and is a product of reactions at pressures lower than the peak recorded pressure. In contrast to low‐ and medium‐pressure granulites, which form at conditions attainable in the mid to lower levels of normal continental crust, high‐pressure granulites (of nonxenolith origin) mostly represent rocks formed as a result of short‐lived tectonic events that led to crustal thickening or subduction of the crust into the mantle. Short times at high‐temperature conditions are reflected in the preservation of prograde zoning in garnet and pyroxene. High‐pressure granulites of both regional types, although rare, are known from both old and young metamorphic terranes (e.g. c. 45 Ma, Namche Barwa, E Himalaya; 400–340 Ma, European Variscides; 1.8 Ga Hengshan, China; 1.9 Ga, Snowbird, Saskatchewan and 2.5 Ga Jianping, China). This spread of ages supports proposals suggesting that thermal and tectonic processes in the lithosphere have not changed significantly since at least the end of the Archean.     

Insights into the complexity of crustal differentiation: K2O‐poor leucosomes within metasedimentary migmatites from the Southern Marginal Zone of the Limpopo Belt,South Africa

Differentiation of the continental crust is the result of complex interactions between a large number of processes, which govern partial melting of the deep crust, magma formation and segregation, and magma ascent to significantly higher crustal levels. The anatectic metasedimentary rocks exposed in the Southern Marginal Zone of the Limpopo Belt represent an unusually well‐exposed natural laboratory where the portion of these processes that operate in the deep crust can be directly investigated in the field. The formation of these migmatites occurred via absent incongruent melting reactions involving biotite, which produced cm‐ to m‐scale, K₂O‐poor garnet‐bearing stromatic leucosomes, with high Ca/Na ratios relative to their source rocks. Field investigation combined with geochemical analyses, and phase equilibrium modelling designed to investigate some aspects of disequilibrium partial melting show that the outcrop features and compositions of the leucosomes suggest several steps in their evolution: (1) Melting of a portion of the source, with restricted plagioclase availability due to kinetic controls, to produce a magma (melt + entrained peritectic minerals in variable proportions relative to melt); (2) Segregation of the magma at near peak metamorphic conditions into melt accumulation sites (MAS), also known as future leucosome; (3a) Re‐equilibration of the magma with a portion of the bounding mafic residuum via chemical diffusion (H₂O, K₂O), which triggers the co‐precipitation of quartz and plagioclase in the MAS; (3b) Extraction of melt‐dominated magma to higher crustal levels, leaving peritectic minerals entrained from the site of the melting reaction, and the minerals precipitated in the MASs to form the leucosome in the source. The key mechanism controlling this behaviour is the kinetically induced restriction of the amount of plagioclase available to the melting reaction. This results in elevated melt H₂O and K₂O and chemical potential gradient for these components across the leucosome/mafic residuum contact. The combination of all of these processes accurately explains the composition of the K₂O‐poor leucosomes. These findings have important implications for our understanding of melt segregation in the lower crust and minimum melt residency time which, according to the chemical modelling, is <5 years. We demonstrate that in some migmatitic granulites, the leucosomes constitute a type of felsic refractory residuum, rather than evidence of failed magma extraction. This provides a new insight into the ways that source heterogeneity may control anatexis.     

Controls on metamorphic equilibration: the importance of intergranular solubilities mediated by fluid composition

A dramatic demonstration of the role of intergranular solubility in promoting chemical equilibration during metamorphism is found in the unusual zoning of garnet in pelitic schist exposed at Harpswell Neck, Maine, USA. Many garnet crystals have irregular, patchy distributions of Mn, Cr, Fe and Mg in their inclusion‐rich interiors, transitioning to smooth, concentric zoning in their inclusion‐poor outer rims; in contrast, zoning of Ca and Y is comparatively smooth and concentric throughout. We re‐assess the disputed origin of these zoning features by examining garnet growth in the context of the thermal and structural history of the rocks, and by evaluating the record of fluid–rock interaction revealed in outcrop‐scale veining and fluid‐inclusion assemblages. The transition in the character of garnet zoning correlates with the onset of a synkinematic, simple‐shear‐dominated phase of garnet growth and with a shift in the composition of the intergranular fluid from CO₂‐rich to H₂O‐rich. Compositional variations in garnet are therefore best explained by a two‐stage growth history in which intergranular diffusive fluxes reflect differences in the concentration of dissolved species in these two contrasting fluids. Interiors of garnet crystals grew in the presence of a CO₂‐rich fluid, in which limited solubility for Mn and Cr (and perhaps Fe and Mg) produced patchy disequilibrium overprint zoning, while appreciable solubility for Ca and Y permitted their rock‐wide equilibration. Rims grew in the presence of an H₂O‐rich fluid, in which high intergranular concentrations for all elements except Cr enabled diffusion over length scales sufficient for rock‐wide equilibration. This striking example of partial chemical equilibrium during reaction and porphyroblast growth implies that thermal effects may commonly be subsidiary in importance to solubilities in the intergranular medium as determinants of length scales for metamorphic equilibration.     

U–Th–Pb monazite dating and the timing of arc–continent collision in East Timor

The Timor Orogen represents one of the youngest arc–continent collisions exposed on the Earth. It has the potential to provide some of the key parameters about how this style of orogeny evolves. However, the metamorphic age of the highest-grade rocks formed in the collision remains controversial. Using U–Th–Pb dating of monazite from amphibolite-grade sillimanite and garnet-bearing schists we show the peak metamorphism occurred at 5.5–4.7 Ma. The young age of the monazite and the presence of significant amounts of common Pb required the development of a new protocol to simultaneously account for the ²³⁰Th disequilibrium and the ²⁰⁷Pb common Pb correction. The new estimate of metamorphic age is consistent with the estimates based on plate reconstructions for the initiation of arc–continent collision in East Timor. The metamorphic event is a result of this collision.     

Archean (about 2500 Ma) anatexis in eastern North China Block

Two Neoarchean alkaline feldspar-rich granites sourced from partially melted granulite-facies granodioritic orthogneiss have been here recognised in the eastern part of the North China Block (NCB). These poorly foliated granites have previously been assumed to be Mesozoic in age and never dated, and so their significance has not been recognised until now. The first granite (AG1) is a porphyritic syenogranite with megacrystic K-feldspar, and the second (AG2) is a quartz syenite with perthitic megacryst. Zircons from the granites yield LA-ICP-MS U-Pb ages of 2499 ± 10 Ma (AG1), and 2492 ± 28 Ma (AG2), which are slightly younger than the granodioritic orthogneiss that they intrude with a crystallisation U-Pb age of 2537 ± 34 Ma. The younger granites have higher assays for SiO₂ (71.91% for AG1 and 73.22% for AG2) and K₂O (7.52% for AG1 and 8.37% for AG2), and much lower assays for their other major element than the granodioritic orthogneiss. All of the granodioritic orthogneiss and granite samples have similar trace element patterns, with depletion in Th, U, Nb, and Ti and enrichment in Rb, Ba, K, La, Ce, and P. This indicates that the granites are derived from the orthogneiss as partial melts. Although they exhibit a similar REE pattern, the granites have much lower total REE contents (30.97×10⁻⁶ for AG1, and 25.93×10⁻⁶ for AG2), but pronounced positive Eu anomalies (Eu/Eu* = 8.57 for AG1 and 27.04 for AG2). The granodioritic orthogneiss has an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70144, εNd(t) value of 3.5, and εHf(t) values ranging from −3.2 to +2.9. The orthogneiss is a product of fractional crystallisation from a dioritic magma, which was derived from a mantle source contaminated by melts derived from a felsic slab. By contrast, the AG1 sample has an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.6926 that is considered too low in value, εNd(t) value of 0.3, and εHf(t) values between +0.57 and +3.82; whereas the AG2 sample has an initial ⁸⁷Sr/⁸⁶Sr ratio of 0.70152, εNd(t) value of 1.3, and εHf(t) values between +0.5 and +14.08. These assays indicate that a Sr-Nd-Hf isotopic disequilibrium exists between the granite and granodioritic orthogneiss. The elevated εHf(t) values of the granites can be explained by the involvement of Hf-bearing minerals, such as orthopyroxene, amphibole, and biotite, in anatectic reactions in the granodioritic orthogneiss. Based on the transitional relationship between the granites and granodioritic orthogneiss and the geochemical characteristics mentioned above, it is concluded that the granites are the product of rapid partial-melting of the granodioritic orthogneiss after granulite-facies metamorphism, and their crystallisation age of about 2500 Ma provides the minimum age of the metamorphism. This about 2500 Ma tectonic-metamorphic event in NCB is similar to the other cratons in India, Antarctica, northern and southern Australia, indicating a possible connection between these cratons during the Neoarchean.     

The application of uranium series disequilibrium concepts to sediment yield determination

The determination of uranium series disequilibria in fluvial environments is proposed as a method of calculating catchment mass balances. The technique is based on two main principles. Firstly, ²³⁴U is more mobile than ²³⁸U, especially during the early stages of weathering. Secondly, uranium is far more mobile than either thorium or protactinium. Consequently, teaching during weathering results in the loss of the uranium found in the fresh rock, leaving the two immobile daughters behind. The ratio of uranium carried by sediment to that dissolved, U_S/U_W can, therefore, be determined from river water and sediment isotopic activity ratios. Fluxes of uranium can then be calculated from average concentrations in the water and the associated sediment, from which a sediment yield can be inferred. The Witham catchment in Lincolnshire has been used to test the proposed method. A U_S/U_W ratio of between 5 and 7 is determined and a sediment yield of 2.51 ± 2.12 tonnes yr^?1 km^?2 is proposed. Although some problems concerning environmental chemistry have arisen, the validity of the approach is confirmed by the close correspondence between the results obtained and those inferred by earlier workers using more conventional methods.     

皖南东至金矿化域中载金硫化物的非平衡性研究

绝大多数的金矿化作用都是在非平衡的开放体系中完成的,再加上硫化物在结晶过程中生长速度过快,因此难免产生一些异常特征:晶格金在硫化物中大量出现、含金硫化物单晶中主元素含量变化很大以及主族元素Si加入硫化物晶格等。这些异常特征在皖南东至金矿化区得到了良好的体现,其成因是不能用经典的平衡态热力学和晶体化学理论来解释的。     

高精度热电离质谱(TIMS)铀系法洞穴沉积物(石笋)年龄的研究

用高精度热电离质谱技术测定石笋的年龄,初步建立了热电离质谱铀系年龄的方法。 4个样品的测定结果复现性较好,铀含量、同位素比值及年龄值与标准值吻合,数据的精度大大提高,显示了质谱铀系年龄方法具有样品量少、时间短、精度高的优点。     

水－岩反应的铀系不平衡判别

天然体系中水－岩反应的铀系不平衡判别,是基于水－岩反应使岩石中天然铀衰变系子体核素＾２３４Ｕ,＾２２６Ｒｂ和六价铀的选择性溶失,造成原始放射性平衡遭到不同程度破坏,因而可利用现今测得的岩石中３组核素放射性活度比值Ａ（＾２３４Ｕ）／Ａ（＾２３８Ｕ）,Ａ（＾２３０Ｔｈ）／Ａ（＾２３４Ｕ）和Ａ（＾２２６Ｒａ）／Ａ（＾２３０Ｔｈ）反演判别该岩石曾经历了近代水－岩反应的大致强度和出现,持续时间,这是近十余年     

<Superscript>234</Superscript>Th/<Superscript>238</Superscript>U disequilibrium and particulate organic carbon export in the northern South China Sea

We utilized ²³⁴Th, a naturally occurring radionuclide, to quantify the particulate organic carbon (POC) export rates in the northern South China Sea (SCS) based on data collected in July 2000 (summer), May 2001 (spring) and November 2002 (autumn). Th-234 deficit was enhanced with depth in the euphotic zone, reaching a subsurface maximum at the Chl-a maximum in most cases, as commonly observed in many oceanic regimes. Th-234 was in general in equilibrium with ²³⁸U at a depth of ∼100 m, the bottom of the euphotic zone. In this study the ²³⁴Th deficit appeared to be less significant in November than in July and May. A surface excess of ²³⁴Th relative to ²³⁸U was found in the summer over the shelf of the northern SCS, most likely due to the accumulation of suspended particles entrapped by a salinity front. Comparison of the ²³⁴Th fluxes from the upper 10 m water column between 2-D and traditional 1-D models revealed agreement within the errors of estimation, suggesting the applicability of the 1-D model to this particular shelf region. 1-D model-based ²³⁴Th fluxes were converted to POC export rates using the ratios of bottle POC to ²³⁴Th. The values ranged from 5.3 to 26.6 mmol C m⁻²d⁻¹ and were slightly higher than those in the southern SCS and other oligotrophic areas. POC export overall showed larger values in spring and summer than in autumn, the seasonality of which was, however, not significant. The highest POC export rate (26.6 mmol C m⁻²d⁻¹) appeared at the shelf break in spring (May), when Chl-a increased and the community structure changed from pico-phytoplankton (<2 μm) dominated to nano-phytoplankton (2–20 μm) and micro-phytoplankton (20–200 μm) dominated.