Pre-Cenozoic intra-plate magmatism along the Central Andes (17–34°S): Composition of the mantle at an active margin

Sr–Nd–Pb isotope ratios of alkaline mafic intra-plate magmatism constrain the isotopic compositions of the lithospheric mantle along what is now the eastern foreland or back arc of the Cenozoic Central Andes (17–34°S). Most small-volume basanite volcanic rocks and alkaline intrusive rocks of Cretaceous (and rare Miocene) age were derived from a depleted lithospheric mantle source with rather uniform initial ¹⁴³Nd/¹⁴⁴Nd ( 0.5127–0.5128) and ⁸⁷Sr/⁸⁶Sr ( 0.7032–0.7040). The initial ²⁰⁶Pb/²⁰⁴Pb ratios are variable (18.5–19.7) at uniform ²⁰⁷Pb/²⁰⁴Pb ratios (15.60 ± 0.05). A variety of the Cretaceous depleted mantle source of the magmatic rocks shows elevated Sr isotope ratios up to 0.707 at constant high Nd isotope ratios. The variable Sr and Pb isotope ratios are probably due to radiogenic growth in a metasomatized lithospheric mantle, which represents the former sub-arc mantle beneath the early Palaeozoic active continental margin. Sr–Nd–Pb isotope signatures of a second mantle type reflected in the composition of Cretaceous (one late Palaeozoic age) intra-plate magmatic rocks (¹⁴³Nd/¹⁴⁴Nd  0.5123, ⁸⁷Sr/⁸⁶Sr  0.704, ²⁰⁶Pb/²⁰⁴Pb  17.5–18.5, and ²⁰⁷Pb/²⁰⁴Pb  15.45–15.50) are similar to the isotopic composition of old sub-continental lithospheric mantle of the Brazilian Shield.

Published Nd and Sr isotopic compositions of Mesozoic to Cenozoic arc-related magmatic rocks (18–40°S) represent the composition of the convective sub-arc mantle in the Central Andes and are similar to those of the Cretaceous (and rare Miocene) intra-plate magmatic rocks. The dominant convective and lithospheric mantle type beneath this old continental margin is depleted mantle, which is compositionally different from average MORB-type depleted mantle. The old sub-continental lithospheric mantle did not contribute to Mesozoic to Cenozoic arc magmatism.     

Predicting groundwater level of wells in the Diyala River Basin in eastern Iraq using artificial neural network

Al-Mansourieh zone is a part of Al-Khalis City within the province of Diyala and located in the Diyala River Basin in eastern Iraq with a total area about 830 km2.Groundwater is the main water source for agriculture in this zone.Random well drilling without geological and hydraulic information has led the most of these wells to dry up quickly.Therefore,it is necessary to estimate the levels of groundwater in wells through observed data.In this study,Alyuda NeroIntelligance 2.1 software was applied to predict the groundwater levels in 244 wells using sets of measured data.These data included the coordinates of wells(x,y),elevations,well depth,discharge and groundwater levels.Three ANN structures(5-3-3-1,5-10-10-1 and 5-11-11-1)were used to predict the groundwater levels and to acquire the best matching between the measured and ANN predicted values.The coefficient of correlation,coefficient determination(R2)and sum-square error(SSE)were used to evaluate the performance of the ANN models.According to the ANN results,the model with the three structures has a good predictability and proves more effective for determining groundwater level in wells.The best predictor was achieved in the structure 5-3-3-1,with R2 about 0.92,0.89,0.84 and 0.91 in training,validation,testing and all processes respectively.The minimum average error in the best predictor is achieved in validation and testing processes at about 0.130 and 0.171 respectively.On the other hand,the results indicated that the model has the potential to determine the appropriate places for drilling the wells to obtain the highest level of groundwater.     

Friedrichbeckeite, K (□0.5Na0.5)2 (Mg0.8Mn0.1Fe0.1)2 (Be0.6 Mg0.4)3 [Si12O30], a new milarite-type mineral from the Bellerberg volcano, Eifel area, Germany

Friedrichbeckeite is a new milarite-type mineral. It was found in a single silicate-rich xenolith from a quarry at the Bellerberg volcano near Ettringen, eastern Eifel volcanic area, Germany. It forms thin tabular crystals flattened on {0001}, with a maximum diameter of 0.6 mm and a maximum thickness of 0.1 mm. It is associated with quartz, tridymite, augite, sanidine, magnesiohornblende, enstatite, pyrope, fluorapatite, hematite, braunite and roedderite. Friedrichbeckeite is light yellow, with white to light cream streak and vitreous lustre. It is brittle with irregular fracture and no cleavage, Mohs hardness of 6, calculated density is 2.686 gcm^?3. Optically, it is uniaxial positive with n_ω = 1.552(2) and n_ε = 1.561(2) at 589.3 nm and a distinct pleochroism from yellow (//ω) to light blue (//ε). Electron microprobe analyses yielded (wt.%): Na₂O 2.73, K₂O 4.16, BeO 4.67, MgO 11.24, MnO 2.05, FeO 1.76, Al₂O₃ 0.15, SiO₂ 73.51, (Σ CaO, TiO₂ = 0.06) sum 100.33 (BeO determined by LA-ICP-MS). The empirical formula based on Si = 12 is K_0.87 Na_0.86 (Mg_1.57Mn_0.28Fe_0.24)_Σ2.09 (Be_1.83?Mg_1.17)_Σ3.00 [Si₁₂O₃₀], and the simplified formula can be given as K (□_0.5Na_0.5)₂ (Mg_0.8Mn_0.1Fe_0.1)₂ (Be_0.6?Mg_0.4)₃ [Si₁₂O₃₀]. Friedrichbeckeite is hexagonal, space-group P6/mcc, with a = 9.970(1), c = 14.130(3) Å, V = 1216.4(3) ų, and Z = 2. The strongest lines in the X-ray powder diffraction pattern are (d in Å / I _obs / hkl): 3.180 / 100 / 121, 2.885 / 70 / 114, 4.993 / 30 / 110, 4.081 / 30 / 112, 3.690 / 30 / 022. A single-crystal structure refinement (R1 = 3.62 %) confirmed that the structure is isotypic with milarite and related ^[12] C ^[9] B ₂ ^[6] A ₂ ^[4] T2₃ [^[4] T1₁₂O₃₀] compounds. The C-site is dominated by potassium, the B-site is almost half occupied by sodium, and the A-site is dominated by Mg. The site-scattering at the T2-site can be refined to a Be/(Be?+?Mg) value close to 0.61; the T1-site is occupied by Si. Micro-Raman spectroscopy reveals an increasing splitting of scattering bands around 550 cm^?1 for friedrichbeckeite. The mineral can be classified as an unbranched ring silicate or as a beryllo-magnesiosilicate. With respect to the end-member formula K (□0.5Na0.5)₂ Mg₂ Be₃ [Si₁₂O₃₀] friedrichbeckeite represents the Mg-dominant analogue of almarudite, milarite or oftedalite. The mineral and its paragenesis were formed during pyrometamorphic modifications of the silicate-rich xenoliths enclosed in Quaternary leucite-tephritic lava of the Bellerberg volcano. Holotype material of friedrichbeckeite has been deposited at the mineral collection of the Naturhistorisches Museum Wien, Austria. The mineral is named friedrichbeckeite in honour of the Austrian mineralogist and petrographer Friedrich Johann Karl Becke (1855–1931).     

The Khan-Taishir ophiolitic complex of Western Mongolia,its petrology,origin and comparison with other ophiolitic complexes

The Khan-Taishir ophiolitic complex is situated within Early Caledonian structures of Western Mongolia. It consists (from below upward) of strongly differentiated ultramafics (dunites and harzburgites), pyroxenites and gabbro, sheeted dikes, pillow lavas and sediments, including in their uppermost part archaeocyatic limestones of Lower Cambrian age. Geological, petrochemical and geochemical data indicate that the ultramafics are turn off from the overlying ophiolitic sequence. Igneous rocks of the ophiolitic complex, except the ultramafics, were formed by two-stage differentiation of mantle magma of quartz-tholeiitic composition exhausted in potassium and titanium. Pyroxenites and gabbro with an anorthositic trend of differentiation were generated during the first stage, and sheeted dikes and pillow lavas with a quartz trend of differentiation were formed during the second one. Ophiolites of the Khan-Taishir complex petrochemically and geochemically differ strongly from mafic and ultramafic rocks of midoceanic ridges. Together with ophiolites of the Troodos complex (Cyprus) and Macquarie Island (eastern Indian Ocean) they constitute the special type of ophiolite peculiar rather to slip boundaries of lithosphere plates. The other type of ophiolite, including complexes like the Dzolen complex of south Mongolia, contains poorly differentiated ultramafics and does not contain sheeted dikes; while the igneous rocks are very similar to mafic and ultramafic rocks dredged from midoceanic and formed probably in midoceanic ridge environments as well.     

Removal of chromium (VI) from aqueous solutions using Lewatit FO36 nano ion exchange resin

The removal of the chromium (VI) ion from aqueous solutions with the Lewatit FO36 ion-exchange resin is described at different conditions. The effects of adsorbent dose, initial metal concentration, contact time and pH on the removal of chromium (VI) were investigated. The batch ion exchange process was relatively fast and it reached equilibrium after about 90 min of contact. The ion exchange process, which is pH dependent showed maximum removal of chromium (VI) in the pH range 5.0–8.0 for an initial chromium (VI) concentration of 0.5 mg/dm³. The equilibrium related to Lewatit FO36 ion- exchange capacity and the amounts of the ion exchange were obtained using the plots of the Langmuir adsorption isotherm. It was observed that the maximum ion exchange capacity of 0.29 mmol of chromium (VLVg for Lewatit FO36 was achieved at optimum pH value of 6.0. The ion exchange of chromium (VI) on this cation-exchange resin followed first-order reversible kinetics.     

夏季不同天气背景和灌溉条件下绿洲地表辐射和能量平衡特征

利用2005年"绿洲系统能量和水分循环过程"野外观测实验(JTEX)资料,分析了夏季不同天气背景下的金塔绿洲小气候特征、辐射和能量平衡特征的日变化规律.结果表明:不同天气和土壤湿度背景下的辐射和能量平衡特征有较大差异.观测中发现有较大的能量不平衡差额,晴天时的能量亏损大于阴天的.     

土壤酶对碘离子在土壤中吸附行为的影响

以批式试验法研究了微生物、葡萄糖氧化酶、脲酶、纤维素酶及其催化底物葡萄糖、尿素和纤维素对Ⅰ-在土壤中吸附的影响,结果表明微生物能显著提高Ⅰ-吸附量,但葡萄糖氧化酶、脲酶、纤维素酶及葡萄糖、尿素和纤维素对Ⅰ-吸附并无促进作用.葡萄糖氧化酶及葡萄糖含量在小于100 mg/L时对Ⅰ-吸附无影响,1000 mg/L时与Ⅰ-呈竞争吸附;脲酶及尿素随浓度增大,对Ⅰ-吸附的抑制作用变得明显;1～1000 mg/L范围内,纤维素酶和纤维素对Ⅰ-吸附没有影响;但葡萄糖氧化酶和葡萄糖生成的中间产物可促进土壤对Ⅰ-的吸附.平衡液中溶解性有机碳(DOC)含量随时间增加而逐渐降低,有机质浓度越大,降低趋势越明显.     

GGR Biennial Critical Review: Analytical Developments Since 2014

This GGR biennial critical review covers developments and innovations in key analytical methods published since January 2014, relevant to the chemical, isotopic and crystallographic characterisation of geological and environmental materials. In nine selected analytical fields, publications considered to be of wide significance are summarised, background information is provided and their importance evaluated. In addition to instrumental technologies, this review also presents a summary of new developments in the preparation and characterisation of rock, microanalytical and isotopic reference materials, including a précis of recent changes and revisions to ISO guidelines for reference material characterisation and reporting. Selected reports are provided of isotope ratio determinations by both solution nebulisation MC‐ICP‐MS and laser ablation‐ICP‐MS, as well as of radioactive isotope geochronology by LA‐ICP‐MS. Most of the analytical techniques elaborated continue to provide new applications for geochemical analysis; however, it is noted that instrumental neutron activation analysis has become less popular in recent years, mostly due to the reduced availability of nuclear reactors to act as a neutron source. Many of the newer applications reported here provide analysis at increasingly finer resolution. Examples include atom probe tomography, a very sensitive method providing atomic scale information, nanoscale SIMS, for isotopic imaging of geological and biological samples, and micro‐XRF, which has a spatial resolution many orders of magnitude smaller than conventional XRF.     

Hydration and phase relations of grossular-spessartine garnets at P H 2O=2 Kb

The phase relations in the system grossular-spessartine-H₂O were investigated at 2.0 Kb aqueous fluid pressure and at subsolidus temperatures down to 420 ° C. Despite metastable persistence of a compositional gap found in some intermediate members, a complete solid solution between grossular and spessartine exists.Linear relations between the unit cell edge, a ₀, and composition were readily observed down to 620 ° C with a ₀=11.849(2) Å and 11.613(2) Å for grossular and spessartine, respectively. Hydrated garnets began to appear at higher temperature for the Ca-rich members. Grossular and spessartine formed at 420 ° C have a ₀=11.901(2) Å and 11.632(2) Å, indicating the presence of 0.6 and 0.2 mol H₂O, respectively. Intermediate members show varying degrees of hydration. Infrared spectra of the more hydrated members show a major and minor absorption bands at 3,620 cm^–1 and 3,660 cm^–1, respectively, in addition to a broad band around 3,430 cm^–1. All the hydrogarnets formed at 420 ° C were proven to be metastable.The rare occurrence of the intermediate grossular-spessartine garnets may be attributed to the lack of appropriate bulk chemistry of the rock rather than to the P-T conditions to which the rock is subjected. There may be a stability field for hydrogrossular below 420 ° C at 2 Kb, but not for hydrospessartine. Any occurrence of hydrogarnet may be used as a temperature indicator setting the maximum of formation for the hydrogarnet-bearing assemblage below 420 ° C at 2 Kb.     

黑龙江太平岭早侏罗世花岗岩成因及壳幔混合作用

位于黑龙江省牡丹江一带的太平岭是兴蒙造山带的重要组成部分,在该区广泛分布大量花岗岩。这些花岗岩的SHRIMP锆石U-Pb年龄介于179～204 Ma之间,表明形成于早侏罗世,而非以往认为的晚三叠世。岩体的岩性以花岗闪长岩为主,其中普遍含有细粒闪长质包体,而二长花岗岩-正长花岗岩中偶见细粒闪长质包体。岩石学、岩相学和地球化学研究表明这些花岗岩为壳幔岩浆混合成因。太平岭早侏罗世花岗岩具有比较均一的Sr、Nd、Pb同位素成分,εNd(t)值介于-3.2～+2.3之间,(87Sr/86Sr)i值主要集中在0.704～0.706之间,进一步表明岩石的源区与幔源物质有密切的联系。花岗岩显示火山弧花岗岩的特点,代表了以挤压为主的构造环境,表明岩石可能与古太平洋板块俯冲作用有关。