Magmatic Evolution of the La Pacana Caldera System, Central Andes, Chile: Compositional Variation of Two Cogenetic, Large-Volume Felsic Ignimbrites

La Pacana is one of the largest known calderas on Earth, andis the source of at least two major ignimbrite eruptions witha combined volume of some 2700 km³. These ignimbrites have stronglycontrasting compositions, raising the question of whether theyare genetically related. The Toconao ignimbrite is crystal poor,and contains rhyolitic (76–77 wt % SiO₂) tube pumices.The overlying Atana ignimbrite is a homogeneous tuff whose pumiceis dacitic (66–70 wt % SiO₂), dense (40–60% vesicularity)and crystal rich (30–40 % crystals). Phase equilibriaindicate that the Atana magma equilibrated at temperatures of770–790°C with melt water contents of 3·1–4·4wt %. The pre-eruptive Toconao magma was cooler (730–750°C)and its melt more water rich (6·3–6·8 wt% H₂O). A pressure of 200 MPa is inferred from mineral barometryfor the Atana magma chamber. Isotope compositions are variablebut overlapping for both units (⁸⁷Sr/⁸⁶Sr_i 0·7094–0·7131;¹⁴³Nd/¹⁴⁴Nd 0·51222–0·51230) and are consistentwith a dominantly crustal origin. Glass analyses from Atanapumices are similar in composition to those in Toconao tubepumices, demonstrating that the Toconao magma could representa differentiated melt of the Atana magma. Fractional crystallizationmodelling suggests that the Toconao magma can be produced by30% crystallization of the observed Atana mineral phases. Toconaomelt characteristics and intensive parameters are consistentwith a volatile oversaturation-driven eruption. However, thelow H₂O content, high viscosity and high crystal content ofthe Atana magma imply an external eruption trigger. KEY WORDS: Central Andes; crystal-rich dacite; eruption trigger; high-silica rhyolite; zoned magma chamber     

Varved sediments of Lake Yoa (Ounianga Kebir,Chad) reveal progressive drying of the Sahara during the last 6100 years

The sedimentological and geochemical properties of a 7·47 m long laminated sequence from hypersaline Lake Yoa in northern Chad have been investigated, representing a unique, continuous 6100 year long continental record of climate and environmental change in the eastern Central Sahara. These data were used to reconstruct the Mid to Late Holocene history of this currently hyper‐arid region, in order to address the question of whether the Mid Holocene environmental transition from a humid to a dry Sahara was progressive or abrupt. This study involved a suite of analyses, including petrographic and scanning electron microscope examination of thin sections, X‐ray diffraction, X‐radiography, granulometry, loss on ignition and magnetic susceptibility. The potential of micro‐X‐ray fluorescence core scanning was tested at very high resolution. Detailed microscopic investigation revealed the sedimentary processes responsible for the formation of the fine laminations, identified the season during which they were formed, and confirmed their annually rhythmic nature. High‐resolution X‐ray fluorescence core scanning allowed the distinction of each individual lamination over the entire record, opening new perspectives for the study of finely laminated sediment sequences. Geochemical and mineralogical data reveal that, due to decreasing monsoon rainfall combined with continuous and strong evaporation, the hydrologically open and fresh Mid Holocene Lake Yoa slowly evolved into the present‐day hypersaline brine depleted in calcium, which has existed for about the past 1050 years. During the oldest part of the investigated period, Lake Yoa probably contained a permanently stratified lower water column that was nevertheless disrupted relatively frequently by mixing events. Deep‐water anoxia became more stable because of increased salinity‐driven density stratification. In parallel, the sediment grain‐size proxies record a progressive increase of aeolian input in the course of the last 6100 years. Altogether, all geochemical and sedimentological indicators point to a progressive drying of the eastern Central Sahara, strengthening previous conclusions based on palaeoecological indicators.     

Seasonal climate patterns and their influence on calibration of the Hargreaves-Samani equation

Abstract

Annual patterns in climate parameters were studied to evaluate how these influence the quality of reference evapotranspiration (ETo) estimates obtained from the Hargreaves-Samani (HS) equation, since the method only uses the measured temperature directly. The work evaluates how these patterns can be used to improve the HS ETo estimates. Ten-year moving averages from a set of California Irrigation Management Information System (CIMIS) stations were used to evaluate the relationships between solar radiation (R_s), temperature (T) and ETo. The results indicate that T treads behind solar radiation and its value peaks some 25 days later. Thus, the main irrigation season in the Mediterranean climate (1 May–30 September) can be divided into three phases: increasing R_s and T; decreasing R_s with increasing T; and decreasing R_s and T. Non-univocal annual cycles were observed between R_s and T, ETo and R_s, and ETo and T. These annual patterns result in important seasonal changes in the ratio between the HS and Penman-Monteith (FAO PM) ETo estimates. The changes are particularly important during the irrigation season, where the FAO PM initially calculates greater ETo values than the HS methodology, and from the end of May to early September, where the HS equation overestimates the ETo values (by 17 mm, or 3%). These patterns obtained from 2000–2009 data were used to calibrate and improve HS ETo estimates at new sites for the 2010–2011 period. Calibration based on the proposed seasonal region-wide FAO PM/HS ETo ratios improved both the bias (decreased from 0.40 to 0.36 mm d^-1) and r² (increased from 0.67 to 0.87) of the ETo estimates for the irrigation season. The proposed methodology can be easily applied to other regions, even when the existing weather stations are sparse.

Editor Z.W. Kundzewicz     

Laboratory kinetics of C2H radical reactions with ethane, propane, and n-butane at T = 96-296 K: implications for Titan

The kinetics of the reactions of C₂H radical with ethane (k₁), propane (k₂), and n-butane (k₃) are studied over the temperature range of T = 96-296 K with a pulsed Laval nozzle apparatus that utilizes a pulsed laser photolysis-chemiluminescence technique. The C₂H decay profiles in the presence of both the alkane reactant and O₂ are monitored by the CH(A²Δ) chemiluminescence tracer method. The results, together with available literature data, yield the following Arrhenius expressions: k₁(T) = (0.51 ± 0.06) × 10⁻¹⁰ exp[(−76 ± 30)K/T] cm³ molecule⁻¹ s⁻¹ (T = 96-800 K), k₂(T) = (0.98 ± 0.32) × 10⁻¹⁰exp[(−71 ± 60)K/T] cm³ molecule⁻¹ s⁻¹ (T = 96-361 K), and k₃(T) = (1.23 ± 0.26) × 10⁻¹⁰ cm³ molecule⁻¹ s⁻¹ (T = 96-297 K). At T = 296 K, k₁ is measured as a function of total pressure and has little or no pressure dependence. The results from this work support a direct hydrogen abstraction mechanism for the title reactions. Implications to the atmospheric chemistry of Titan are discussed.     

Ultramafic–Mafic Assemblage of Plutonic Rocks and Hornblende Schists of Shirshov Rise,Bering Sea,and Stalemate Ridge,Northwest Pacific: Geodynamic Interpretations of Geochemical Data

The paper presents data on plutonic and metamorphic rocks dredged during Cruise 249 of the German R/V Sonne to the Stalemate Ridge, Northwest Pacific Ocean and the Shirshov Rise, western Bering Sea. Dredges in the northwestern sector of the Stalemate Ridge and central portion of the Shirshov Rise show that the plutonic and metamorphic rocks obtained here are amazingly similar. Our petrologic and geochemical data led us to view the rocks as members of a mafic–ultramafic assemblage typical of cumulate portions of ophiolite complexes and backarc spreading centers. The plutonic complexes of the Shirshov Rise and Stalemate Ridge show similarities not only in the petrography and mineralogy of their protoliths but also in the character of their metamorphic transformations. Plutonic rocks from both areas display mineralogical evidence of metamorphism within a broad temperature range: from the high-temperature amphibolite facies to the greenschist facies. Relations between the index mineral assemblages indicate that the metamorphic history of plutonic complexes in the Stalemate Ridge and Shirshov Rise proceeded along a retrograde path. Hornblende schists accompanying the plutonic rocks of the Stalemate Ridge and Shirshov Rise are petrographically close to foliated amphibolites in subophiolitic metamorphic aureoles. Within the framework of geodynamic interpretations of our results, it is realistic to suggest that the examined plutonic complexes were exhumed from subduction zones of various age.     

Partially Fused Granite Blocks from Mt. Elephant, Victoria, Australia

Petrological and chemical evidence is presented to show thatsmall patches of brown glass found in blocks of granite eruptedin basaltic scoria at Mt. Elephant are the result of the partialfusion of biotite and quartz. The glass has moderate SiO₂ (63–66per cent), high AI₂O₃ (17.5–19 per cent), high FeO (3.8–5.2per cent) and very high K₂O (7.0–7.8 per cent) relativeto Na₂O (3.3–3.7 per cent) and is similar in compositionto many high K alkali syenites and trachytes.     

Revisiting the abandoned shorelines of Lake George,Australia: a refined optical dating framework

Abandoned shorelines are an important archive used to constrain past fluctuations in the hydrological balance of lakes around the globe. Within Australia, the shorelines preserved at Lake George, NSW, form one of the few shoreline archives in the south-east of the continent that record palaeoenvironmental conditions throughout the late Quaternary. Here, we examined and tested the lake-level record for Lake George constructed in the 1970s by dating a well-preserved shoreline sequence at Luckdale, on the lake's eastern shore, using single-grain optically stimulated luminescence (OSL) dating. Ten stratigraphic units were identified, and these suggest a late Quaternary highstand for Lake George in MIS 3, with fluctuations superimposed upon an overall drying trend throughout MIS 2 and into the present. At Luckdale, the highest four shoreline-associated units were deposited ~13 to 19 m above lake base and date to between 39 ± 2 and 29 ± 1 ka ago. Our study pushes back the timing of maximum lake depth at Lake George to at least MIS 3, rather than MIS 2. The overall drying trend is supported by similar reductions in both Riverine Plain fluvial activity and other associated lake-level records from within the Murray basin.     

Uranium (U) concentration and its genetic significance in the phosphorites of the Paleoproterozoic Bijawar Group of the Lalitpur district,Uttar Pradesh,India

The paper presents the uranium (U) concentration and distribution pattern in the Paleoproterozoic phosphorites of Lalitpur district of Uttar Pradesh. The study of thin sections, SEM and XRD reveal that apatite is the essential phosphate mineral while quartz and feldspars are the dominant gangue in the phosphorites of the investigated area. The collophane is observed to be mostly oolitic in form and microspherulitic in texture. The major element geochemistry indicated that the phosphorite samples are rich in P₂O₅, CaO, SiO₂ and Fe₂O₃ whereas depletion of MgO, MnO, K₂O and Al₂O₃ was observed. The CaO/P₂O₅ ratio ranges from 1.13 to 1.46 which is slightly lower than that of cations and anions substituted francolite (1.621) and close to that of carbonate-fluorapatite (1.318). The trace element geochemistry indicates that the phosphorites of Lalitpur have the significant range of U concentration (1.67 to 129.67 μg/g) which is more than that of Th (0.69 to 0.09 μg/g) among the analysed trace elements in the phosphorite samples of the area. The positive correlation of U with P₂O₅, CaO and U/P₂O₅ indicates a close association of U with phosphate minerals like collophane (apatite), whereas negative correlation of U with SiO₂ and Fe₂O₃ may be due to mutual replacement. The antipathetic relationship of U with Ni may be an indication of high oxidizing conditions, whereas sympathetic relationship of U with K₂O points towards higher alkaline conditions of the basin of deposition during phosphatization. The variable concentration of U and its relationship with significant major and trace elements in most of the phosphorite samples lead one to believe that the deposition of these phosphorites might have taken place in highly alkaline medium during fairly oxidizing to weakly reducing environmental conditions of geosynclinal basin.