Composition of barian mica in multiphase solid inclusions from orogenic garnet peridotites as evidence of mantle metasomatism in a subduction zone setting

Multiphase solid inclusions in minerals formed at ultra-high-pressure (UHP) provide evidence for the presence of fluids during deep subduction. This study focuses on barian mica, which is a common phase in multiphase solid inclusions enclosed in garnet from mantle-derived UHP garnet peridotites in the Saxothuringian basement of the northern Bohemian Massif. The documented compositional variability and substitution trends provide constraints on crystallization medium of the barian mica and allow making inferences on its source. Barian mica in the multiphase solid inclusions belongs to trioctahedral micas and represents a solid solution of phlogopite KMg₃(Si₃Al)O₁₀(OH)₂, kinoshitalite BaMg₃(Al₂Si₂)O₁₀(OH)₂ and ferrokinoshitalite BaFe₃(Al₂Si₂)O₁₀(OH)₂. In addition to Ba (0.24–0.67 apfu), mica is significantly enriched in Mg (X_Mg ~ 0.85 to 0.95), Cr (0.03–0.43 apfu) and Cl (0.04–0.34 apfu). The substitution vector involving Ba in the I-site which describes the observed chemical variability can be expressed as BaFe^IVAlClK_?1Mg_?1Si_?1(OH)_?1. A minor amount of Cr and ^VIAl enters octahedral sites following a substitution vector ^VI(Cr,Al)₂□^VI(Mg,Fe)_?3 towards chromphyllite and muscovite. As demonstrated by variable Ba and Cl contents positively correlating with Fe, barian mica composition is partly controlled by its crystal structure. Textural evidence shows that barian mica, together with other minerals in multiphase solid inclusions, crystallized from fluids trapped during garnet growth. The unusual chemical composition of mica reflects the mixing of two distinct sources: (1) an internal source, i.e. the host peridotite and its garnet, providing Mg, Fe, Al, Cr, and (2) an external source, represented by crustal-derived subduction-zone fluids supplying Ba, K and Cl. At UHP–UHT conditions recorded by the associated diamond-bearing metasediments (c. 1100 °C and 4.5 GPa) located above the second critical point in the pelitic system, the produced subduction-zone fluids transporting the elements into the overlying mantle wedge had a solute-rich composition with properties of a hydrous melt. The occurrence of barian mica with a specific chemistry in barium-poor mantle rocks demonstrates the importance of its thorough chemical characterization.     

Apatite-hosted melt inclusions from the Panzhihua gabbroic-layered intrusion associated with a giant Fe–Ti oxide deposit in SW China: insights for magma unmixing within a crystal mush

The ～?2-km-thick Panzhihua gabbroic-layered intrusion in SW China is unusual because it hosts a giant Fe–Ti oxide deposit in its lower zone. The deposit consists of laterally extensive net-textured and massive Fe–Ti oxide ore layers, the thickest of which is ～?60 m. To examine the magmatic processes that resulted in the Fe enrichment of parental high-Ti basaltic magma and the formation of thick, Fe–Ti oxide ore layers, we carried out a detailed study of melt inclusions in apatite from a ～?500-m-thick profile of apatite-bearing leucogabbro in the middle zone of the intrusion. The apatite-hosted melt inclusions are light to dark brown in color and appear as polygonal, rounded, oval and negative crystal shapes, which range from ～?5 to ～?50 µm in width and from ～?5 to ～?100 µm in length. They have highly variable compositions and show a large and continuous range of SiO₂ and FeO_t with contrasting end-members; one end-member being Fe-rich and Si-poor (40.2 wt% FeO_t and 17.7 wt% SiO₂) and the other being Si-rich and Fe-poor (74.0 wt% SiO₂ and 1.20 wt% FeO_t). This range in composition may be attributed to entrapment of the melt inclusions over a range of temperature and may reflect the presence of µm-scale and immiscible Fe-rich and Si-rich components in different proportions. Simulating results for the motion of Si-rich droplets within a crystal mush indicate that Si-rich droplets would be separated from Fe-rich melt and migrate upward due to density differences in the interstitial liquid when the magma unmixed. Migration of the Si-rich, immiscible liquid component from the interstitial liquid caused the remaining Fe-rich melt in the lower part to react with plagioclase primocrysts (An_59–60), as evidenced by fine-grained lamellar intergrowth of An-rich plagioclase (An_79–84)?+?clinopyroxene in the oxide gabbro of the lower zone. Therefore, magma unmixing within a crystal mush, combined with gravitationally driven loss of the Si-rich component, resulted in the formation of Fe-rich, melagabbro and major Fe–Ti oxide ores in the lower part and Si-rich, leucogabbro in the upper part of the intrusion.     

Carbon costs and benefits of France’s biomass energy production targets

Background

Concern about climate change has motivated France to reduce its reliance on fossil fuel by setting targets for increased biomass-based renewable energy production. This study quantifies the carbon costs and benefits for the French forestry sector in meeting these targets. A forest growth and harvest simulator was developed for French forests using recent forest inventory data, and the wood-use chain was reconstructed from national wood product statistics. We then projected wood production, bioenergy production, and carbon balance for three realistic intensification scenarios and a business-as-usual scenario. These intensification scenarios targeted either overstocked, harvest-delayed or currently actively managed stands.

Results

All three intensification strategies produced 11.6–12.4 million tonnes of oil equivalent per year of wood-based energy by 2026, which corresponds to the target assigned to French wood-energy to meet the EU 2020 renewable energy target. Sustaining this level past 2026 will be challenging, let alone further increasing it. Although energy production targets can be reached, the management intensification required will degrade the near-term carbon balance of the forestry sector, compared to continuing present-day management. Even for the best-performing intensification strategy, i.e., reducing the harvest diameter of actively managed stands, the carbon benefits would only become apparent after 2040. The carbon balance of a strategy putting abandoned forests back into production would only break even by 2055; the carbon balance from increasing thinning in managed but untended stands would not break even within the studied time periods, i.e. 2015–2045 and 2046–2100. Owing to the temporal dynamics in the components of the carbon balance, i.e., the biomass stock in the forest, the carbon stock in wood products, and substitution benefits, the merit order of the examined strategies varies over time.

Conclusions

No single solution was found to improve the carbon balance of the forestry sector by 2040 in a way that also met energy targets. We therefore searched for the intensification scenario that produces energy at the lowest carbon cost. Reducing rotation time of actively managed stands is slightly more efficient than targeting harvest-delayed stands, but in both cases, each unit of energy produced has a carbon cost that only turns into a benefit between 2060 and 2080.

     

Fishery-induced Inter-annual Changes in the Mean Trophic Level,the Northern Sea of Oman off the Iranian Coast, 2002–2011

Ecosystem-based management is one of the most important approaches that may lead to reducing the impacts of fishing on ecosystems. In this context, we have assessed the impact of Iranian coastal fishing (using landing data of 49 exploited species) on the ecosystem of the North Sea of Oman (Sistan and Baluchestan Province), during the last decade (2002–2011), with emphasis on testing the occurrence of the “fishing down? phenomenon. The Mean Trophic Level (MTL) and Fishing-in-Balance (FiB) index are two indicators that we used for analysis. The data indicated that the increased total landings in this region might be related to the exploitation of marine fishery resources especially with regard to large pelagic fish. Over the past decade, moderate decreasing trends in MTL and an increasing trend in the FiB-index were observed. In this regard, an upward trend in the spatial expansion factor and also a downward trend in the piscivory index and in Primary Production Required (PPR) in the time period could all indicate a spatial expansion toward deep waters, the catching of the large pelagic piscivorous species, such as tuna, and a sign of fishing pressures on the ecosystem. The results suggest a range of fishery exploitation patterns throughout the food web but it seems that these patterns are not a consequence of ?fishing down?. We suggest that the monitoring research be continued in this region and these indicators should be used to make fisheries management decisions and to prevent the continuance of this trend in future.     

垃圾夯扩短桩在邯郸市的工程实践

本文阐述垃圾夯扩短桩在邯郸新近堆积软土场地上的工程尝试,分析了其加固地基的机理,结合工程实例论述了夯扩短桩在邯郸的适用性及其推广应用前景     

Zur Frage der Altersstellung und Genese der Blei-Zink-Vorkommen der Sierra de Cartagena in Spanien

Zusammenfassung Bleiglanzproben aus verschiedenen Lagerstätten der Sierra de Cartagena wurden auf ihre Blei-Isotopen-Verhältnisse untersucht. Auffallend ist deren völlig identische Pb-Isotopen-Zusammensetzung, aus der sich nach dem Houtermans-Modell ein Modell-Alter von 30 Millionen Jahren errechnen läßt. Die Blei-Mineralisation im Erzdistrikt von Cartagena steht daher in einem sicheren Zusammenhang mit der Tätigkeit jungtertiärer subvulkanischer Magmenherde. Das Alter der Andesite wurde mittels Rb/Sr-Methode an einem Biotit des Atalaya-Andesites mit 44±27 m.y. bestimmt. Dieser Wert stimmt sehr gut mit einer Altersbestimmung an einem leukogranitischen Gang aus der Sierra Cabrera überein (50±3 m.y.). Die Ergebnisse der Spurenelement-bestimmung an Bleiglanzproben werden im Zusammenhang mit schon früher mitgeteilten Schwefel-Isotopen-Daten diskutiert.

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Lead isotope ratios have been determined in galena samples from the Sierra de Cartagena (Spain). The range of the Pb-isotopes is extremely narrow within the ore district, which contains different types of ore deposits. The age of the galena bearing ore deposits has been determined by using the Houtermansmodel: 30 million years. The lead minertalisation in the district therefore may be linked to the subvolcanic activity of Tertiary age. Ascribing the mineralisation to three volcanic episodes of Palaeozoic, Miocene and Pliocene ages and two periodes of supergene processes is not possible. Rb/Sr ratios have been determined in a biotite sample from the Atalaya andesite. The mica age is 44±27 m.y. which is in closest agreement with the age given for rocks in the Sierra Cabrera (50±3 m.y.). The results of trace element analyses are discussed in connection with previously studied sulphur isotope composition.

     

LA CHINE EST-ELLE PLACEE ENTRE DEUX GRANDES FRACTURES DE LA CROUTE TERRESTRE ?

Hest bien clair que toute reponse a cette question, sera du plus haut interet pour les geologues de la Chine, vu que les resultats de la geodesie semblent bien indiquer que la croute terrestre est divisee en plusieurs blocs independants, juxtaposes et equilibres isostatiquement.     

An Example of Island-Arc Petrogenesis: Geochemistry and Petrology of the Southern Luzon Arc, Philippines

Volcanism throughout the Luzon arc is associated with eastwardsubduction of the South China Sea floor along the Manila Trench.The southern section of the arc, the focus of this study, extendsfrom the Lingayen-Dingalan fault to the small islands just southof Luzon. Two segments appear to exist along this section ofthe arc the northern Bataan and southern Mindoro segments whichare separated by the Macolod Corridor. The volcanic rocks have typical arc phenocryst mineralogies:olivine, clinopyroxene, plagioclase, and titanomagnetite inthe most mafic rocks and clinopyroxene, plagioclase, orthopyroxene,titanomagnetite, ? amphibole in the more felsic samples. Complexzoning, sieve textures, and decoupling of incompatible traceelements suggest that processes such as assimilation have takenplace. The rocks from the study area range from basalts to rhyolitesand show typical calc-alkaline features. The rocks of the MacolodCorridor and Mindoro segment are particularly enriched in largeion lithophile elements (LILE), light rare earth elements (LREE),and radiogenic Sr compared with the Bataan segment. The datafall within the mantle array on Sr-Nd isotopic diagrams andgrade toward higher Sr and lower Nd isotopic values from northto south. A likely source for the volcanics of this study is either amid-ocean ridge basalt (MORB)-type mantle that undergoes higherdegrees of partial melting than regions involved in MORB generationor a previously depleted source. We suggest that the high fieldstrength element (HFSE) anomalies have been derived throughdifferential element partitioning during fluid transport fromthe subducted lithosphere to the mantle wedge. Continental crustal material seems to play a significant roleparticularly in the Macolod Corridor and the Mindoro segment,based on the high LILE, La/Sm ratios, radiogenic Sr isotopes,and ¹⁸O values. The Macolod Corridor and the Mindoro segmenthave undergone source contamination by crustal material fromthe North Palawan-Mindoro crustal block either during the collisionof this block with the Manila Trench or by subduction of sedimentsrich in this crustal material. A similar component has alsobeen detected in the Bataan segment but in minor amounts. Thetrace element and isotopic differences between the northernand southern sections of the arc are interpreted in terms ofvariable composition (i. e., variable amounts of a crustal componentintroduced from the Palawan-Mindoro crustal terrain) of themetasomatic fluids released into the source.     

低氟与大骨节病－－大骨节病防治拾趣四则

该文笔者多年研究大骨节病原始原因的一项新说。即病区外环境低氟。引起体内以低氟为中心的代谢紊乱，从而导致以骨骼系统为主的病变－大骨节病。防治该病，应向体外补氟。药疗这一进补方式故然必然，但最有效又生活化的办法是食疗。食疗又分氟盐防治和饮茶防治两种。而最适用且简便的方法是提倡患区人群适度饮茶，并且应从儿时做起。关于补氟和饮茶等防治大骨节病的实践，笔者已浓缩于下面四则拾趣之中……。     

Oxyphlogopite K(Mg,Ti,Fe)3[(Si,Al)4O10](O,F)2: A new mineral species of the mica group

Oxyphlogopite is a new mica-group mineral with the idealized formula K(Mg,Ti,Fe)₃[(Si,Al)₄O₁₀](O,F)₂. The holotype material came from a basalt quarry at Mount Rothenberg near Mendig at the Eifel volcanic complex in Rhineland-Palatinate, Germany. The mineral occurs as crystals up to 4 × 4 × 0.2 mm in size encrusting cavity walls in alkali basalt. The associated minerals are nepheline, plagioclase, sanidine, augite, diopside, and magnetite. Its color is dark brown, its streak is brown, and its luster is vitreous. D _meas = 3.06(1) g/cm³ (flotation in heavy liquids), and D _calc = 3.086 g/cm³. The IR spectrun does not contain bands of OH groups. Oxyphlogopite is biaxial (negative); α = 1.625(3), β = 1.668(1), and γ = 1.669(1); and 2V _meas = 16(2)° and 2V _calc = 17°. The dispersion is strong; r < ν. The pleochroism is medium; X > Y > Z (brown to dark brown). The chemical composition is as follows (electron microprobe, mean of 5 point analyses, wt %; the ranges are given in parentheses; the H₂O was determined using the Alimarin method; the Fe²⁺/Fe³⁺ was determined with X-ray emission spectroscopy): Na₂O 0.99 (0.89–1.12), K₂O 7.52 (7.44–7.58), MgO 14.65 (14.48–14.80), CaO 0.27 ((0.17–0.51), FeO 4.73, Fe₂O₃ 7.25 (the range of the total iron in the form of FeO is 11.09–11.38), Al₂O₃ 14.32 (14.06–14.64), Cr₂O₃ 0.60 (0.45–0.69), SiO₂ 34.41 (34.03–34.66), TiO₂ 12.93 (12.69–13.13), F 3.06 (2.59–3.44), H₂O 0.14; O=F₂ −1.29; 99/58 in total. The empirical formula is (K_0.72Na_0.14Ca_0.02)(Mg_1.64Ti_0.73Fe_0.30²⁺ Fe_0.27³⁺Cr_0.04)_Σ2.98(Si_2.59Al_1.27Fe_0.14³⁺ O₁₀) O_1.20F_0.73(OH)_0.07. The crystal structure was refined on a single crystal. Oxyphlogopite is monoclinic with space group C2/m; the unit-cell parameters are as follows: a = 5.3165(1), b = 9.2000(2), c = 10.0602(2) ?, β = 100.354(2)°. The presence of Ti results in the strong distortion of octahedron M(2). The strongest lines of the X-ray powder diffraction pattern [d, ? (I, %) [hkl]] are as follows: 9.91(32) [001], 4.53(11) 110], 3.300(100) [003], 3.090(12) [112], 1.895(21) [005], 1.659(12) [−135], 1.527(16) [−206, 060]. The type specimens of oxyphlogopite are deposited at the Fersman Mineralogical Museum in Moscow, Russia; the registration numbers are 3884/2 (holotype) and 3884/1 (cotype).