Architecture and evolution of the Paine channel complex, Cerro Toro Formation (Upper Cretaceous), Silla Syncline, Magallanes Basin, Chile

The Upper Cretaceous Cerro Toro Formation in the Silla Syncline, Parque Nacional Torres del Paine, Magallanes Basin, Chile, includes over 1100 m of mainly thin‐bedded mud‐rich turbidites containing three thick divisions of coarse conglomerate and sandstone. Facies distributions, stacking patterns and lateral relationships indicate that the coarse‐grained sandstone and conglomerate units represent the fill of a series of large south to south‐east trending deep‐water channels or channel complexes. The middle coarse division, informally named the Paine member, represents the fill of at least three discrete channels or channel complexes, termed Paine A, B and C. The uppermost of these, Paine C, represents a channel belt about 3·5 km wide and its fill displays explicit details of channel geometry, channel margins, and the processes of channel development and evolution. Along its northern margin, Paine C consists of stacked, laterally offset channels, each eroded into fine‐grained mudstone and thin‐bedded sandy turbidites. Along its southern margin, the Paine C complex was bounded by a single, deeply incised but stepped erosional surface. The evolution of the Paine C channel occurred through multiple cycles of activity, each involving: (i) an initial period of channel erosion into underlying fine‐grained sediments; (ii) deposition of coarse‐grained pebble to cobble conglomerate and sandstone within the channel; and (iii) waning of coarse sediment deposition and accumulation of a widespread sheet of fine‐grained, thin‐bedded turbidites inside and outside the channel. The thin‐bedded turbidites deposited within, and adjacent to, the channel along the northern margin of the Paine C complex do not appear to represent levée deposits but, rather, a separate fine‐grained turbidite system that impinged on the Paine C channel from the north. The Cerro Toro channel complex in the Silla Syncline may mark either an early axial zone of the Magallanes Basin or a local slope mini‐basin developed behind a zone of slope faulting and folding now present immediately east of the syncline. If the latter, flows moving downslope toward the basin axis further east were diverted to the south by this developing structural high, deposited part of their coarse sediment loads, and exited the mini‐basin at a point located near the south‐eastern edge of the present Silla Syncline.     

Time relationships between volcanism–plutonism–alteration–mineralization in Cu-stratabound ore deposits from the Michilla mining district,northern Chile: a <Superscript>40</Superscript>Ar/<Superscript>39</Superscript>Ar geochronological approach

The Michilla mining district comprises one of the most important stratabound and breccia-style copper deposits of the Coastal Cordillera of northern Chile, hosted by the Middle Jurassic volcanic rocks of the La Negra Formation. ⁴⁰Ar/³⁹Ar analyses carried out on igneous and alteration minerals from volcanic and plutonic rocks in the district allow a chronological sequence of several magmatic and alteration events of the district to be established. The first event was the extrusion of a thick lava series of the La Negra Formation, dated at 159.9 ± 1.0 Ma (2σ) from the upper part of the series. A contemporaneous intrusion is dated at 159.6 ± 1.1 Ma, and later intrusive events are dated at 145.5 ± 2.8 and 137.4 ± 1.1 Ma, respectively. Analyzed alteration minerals such as adularia, sericite, and actinolite apparently give valid ⁴⁰Ar/³⁹Ar plateau and miniplateau ages. They indicate the occurrence of several alteration events at ca. 160–163, 154–157, 143–148, and 135–137 Ma. The first alteration event, being partly contemporaneous with volcanic and plutonic rocks, was probably produced in a high thermal gradient environment. The later events may be related either to a regional low-grade hydrothermal alteration/metamorphism process or to plutonic intrusions. The Cu mineralization of the Michilla district is robustly bracketed between 163.6 ± 1.9 and 137.4 ± 1.1 Ma, corresponding to dating of actinolite coexisting with early-stage chalcocite and a postmineralization barren dyke, respectively. More precisely, the association of small intrusives (a dated stock from the Michilla district) with Cu mineralization in the region strongly suggests that the main Michilla ore deposit is related to a magmatic/hydrothermal event that occurred between 157.4 ± 3.6 and 163.5 ± 1.9 Ma, contemporaneous or shortly after the extrusion of the volcanic sequence. This age is in agreement with the Re–Os age of 159 ± 16 Ma obtained from the mineralization itself (Tristá-Aguilera et al., Miner Depos, 41:99–105,2006).     

Francisco José de Caldas's Unaccomplished Life-Project – His Map Provincias Unidas de la Nueva Granada, 1811/ 1815

The first attempted republican map of present-day Colombia remained unachieved. Francisco José de Caldas worked on it since 1797 and, come the revolution and Nueva Granada's republican inception, he prepared two successive cartouches to introduce it: the first one in 1811, the latter in 1815. Finally entitled Provincias de la Nueva Granada, Caldas's map remains understudied. In this article, I establish its basic cartographic parameters, discuss the political context of its unfinished making and link it to its pertinent cartographic precedents.     

Late-glacial and early Holocene lake sediments,ground-water formation and climate in the Atacama Altiplano 22–24°S

Precipitation rates in the Atacama Altiplano 22–24°S were 400–500 mm yr^–1 during late glacial and early Holocene times as opposed to 200 mm yr^–1 today. This humid phase (Tauca phase) was likely due to strengthened tropical (monsoonal) circulation, which brought continental moisture to the Atacama Altiplano. The lake level of Laguna Lejía (23°30S, 4350 m) at that time was up to 25 m higher than it is today. Mg/Ca and Sr/Ca data from lake sediments show that, what today is a highly saline lake was a freshwater lake at that time. Seasonally-laminated calcareous sediments were deposited between 13 500 and <10 400 yr B.P. indicating the maximum of the humid phase. Climatic changes in the past are important for current groundwater resources.¹⁴C and³H data from lake-, ground- and well water suggest that modern groundwater formation (i.e. water <40 years) in the Altiplano is very limited under current arid conditions. We conclude that significant amounts of the water resources in this area originated during the time of the late-glacial and early Holocene humid climate. Tritium data from snow samples show that the moisture in the Altiplano at 22–24°S is mainly of continental origin, whereas precipitation from the westerlies hardly contributes to the water supply in this area. This precipitation pattern matches the paleodata, and we suggest that current precipitation formation may provide an analogue framework for late-glacial circulation in this area.This is the 3rd in a series of papers published in this special AMQUA issue. These papers were presented at the 1994 meeting of the American Quaternary Association held 19–22 June, 1994, at the University of Minnesota, Minneapolis, Minnesota, USA. Dr Linda C. K. Shane served as guest editor for these papers.     

Cretaceous amber inclusions of Spain and Myanmar demonstrate early diversification and wide dispersal of Cephenniitae (Coleoptera: Staphylinidae: Scydmaeninae)

The taxonomic status of previously misplaced species of an ant-like stone beetle from Spanish amber (Albian) is clarified. Specimens of Kachinus magnificus (originally placed as incertae sedis within Scydmaenitae) were re-examined and their characters were found different from those of the type species of Kachinus from Myanmar amber. Consequently, Archeutheia gen. nov. is proposed to accommodate the Spanish species, resulting in Archeutheia magnifica comb. nov. Moreover, in a comprehensive phylogenetic analysis Archeutheia was placed as a sister group to extant Eutheia, within the tribe Eutheiini of Cephenniitae. A specimen of an undetermined genus from Myanmar amber clearly belonging in Cephenniini is also recorded. Both taxa represent the first definite Cretaceous Cephenniitae, a supertribe whose recent members are distributed on all continents but are especially diverse in the Oriental and East Palaearctic regions. This finding demonstrates a diversification of two presently most species-rich tribes of Cephenniitae already in Early Cretaceous. Archeutheia is strikingly similar to the extant species of Eutheia and Veraphis, showing male dimorphic characters (modified protrochanters) and antennal cavities characteristic of Palaearctic Eutheiini. This fact suggests a long morphological stability in the supertribe. A previously proposed hypothesis of an early presence of the Cephenniitae in the Northern Hemisphere is for the first time supported by the fossil record, and the palaeolocalities (western Europe and Southeast Asia) demonstrate a wide distribution of Cephenniitae in the Cretaceous and an early split of its ancestral lineage.     

Secondary Ion Mass Spectrometry Bias on Isotope Ratios in Dolomite–Ankerite,Part II: δ13C Matrix Effects

This study is Part II of a series that documents the development of a suite of calibration reference materials for in situ SIMS analysis of stable isotope ratios in Ca‐Mg‐Fe carbonates. Part I explored the effects of Fe²⁺ substitution on SIMS δ¹⁸O bias measured from the dolomite–ankerite solid solution series [CaMg(CO₃)₂–CaFe(CO₃)₂], whereas this complementary work explores the compositional dependence of SIMS δ¹³C bias (calibrated range: Fe# = 0.004–0.789, where Fe# = molar Fe/(Mg+Fe)). Under routine operating conditions for carbonate δ¹³C analysis at WiscSIMS (CAMECA IMS 1280), the magnitude of instrumental bias increased exponentially by 2.5–5.5‰ (session‐specific) with increasing Fe‐content in the dolomite structure, but appeared insensitive to minor Mn substitution [< 2.6 mole % Mn/(Ca+Mg+Fe+Mn)]. The compositional dependence of bias (i.e., the matrix effect) was expressed using the Hill equation, yielding calibration residual values ≤ 0.3‰ relative to CRM NBS‐19 for eleven carbonate reference materials (6‐μm‐diameter spot size measurements). Based on the spot‐to‐spot repeatability of a drift monitor material that ‘bracketed’ each set of ten sample‐spot analyses, the analytical precision was ± 0.6–1.2‰ (2s, standard deviations). The analytical uncertainty for individual sample analyses was approximated by combining the precision and calibration residual values (propagated in quadrature), suggesting an uncertainty of ± 1.0–1.5‰ (2s).     

Precise and Accurate Doping of Nanoporous Silica Gel for the Synthesis of Trace Element Microanalytical Reference Materials

This study presents an experimental procedure to fabricate high‐purity silica glass containing a selected element at a specified mass fraction. The procedure was used to prepare glasses doped with trace‐level mass fractions of Ti with the goal of improving analytical confidence when measuring trace elements in quartz. Systematic tests were performed to determine the ideal conditions and procedures for doping nanoporous silica gel with the highest efficiency of dopant recovery. Silica gel was cleaned in concentrated HCl, immersed in a non‐polar doping medium at a controlled pH and doped with precise quantities of ICP‐MS standard solution. Using liquids composed of longer chain molecules as the doping medium diminishes recovery, suggesting that large molecules could obstruct nanopores to inhibit capillary uptake of the dopant. A control experiment using crystalline quartz reinforced the effectiveness of nanoporous silica gel for doping with trace‐level precision. Layered aggregates of silica gel doped with different Ti mass fractions were hot‐pressed to create multi‐layered reference materials that were analysed with multiple techniques at a variety of spatial scales. Analyses at the intra‐grain scale (cathodoluminescence scanning electron microscopy, electron probe microanalysis), at the single grain scale (SIMS), at the sample layer scale (EPMA, laser ablation‐ICP‐MS) and at the bulk scale (ICP‐OES) demonstrated acceptable homogeneity at sample volumes characteristic of most microanalysis techniques and show that nanoporous silica gel holds promise as a highly retentive doping substrate for preparing reference materials for laser‐, electron‐ and ion‐beam microanalysis.     

Appropriate Sampling for Optimised Measurement (ASOM), rather than the Theory of Sampling (TOS) Approach,to Ensure Suitable Measurement Quality: A Refutation of Esbensen and Wagner (2014)

The ‘Appropriate Sampling for Optimised Measurement’ (ASOM) approach considers measurement to be the focus of the sampling process, and sampling to be only the first part of the measurement process. To achieve ASOM, the uncertainty of measurements, including its contribution from sampling, needs to be estimated and optimised in order to achieve fitness‐for‐purpose. Such samples are then ‘sufficiently’ representative. The ‘Theory of Sampling’ (TOS) focuses on the processes of primary sampling and sample preparation and assumes that samples are ‘representative’ if they are correctly prepared by nominally ‘correct’ protocols. It defines around ten sampling ‘errors’, which are either modelled or minimised to improve sampling quality. It is argued that the ASOM approach is more effective in achieving appropriate measurement quality than in applying TOS to just the first part of the measurement process. The comparison is made less effective by the different objectives, scopes, terminology and assumptions of the two approaches. ASOM can be applied to in situ materials that are too variable to be modelled accurately, or where sources of uncertainty are unsuspected. The proposed integration of ASOM with TOS (Esbensen and Wagner 2014, Trends in Analytical Chemistry, 57, 93–106) is therefore effectively impossible. However, some TOS procedures can be useful within the ASOM approach.     

Elimination of Interferences in the Determination of Palladium,Platinum and Rhodium Mass Fractions in Moss Samples using ICP‐MS/MS

Moss samples (Pleurozium schreberi) exposed to traffic‐related emission of Pd, Pt and Rh were analysed in this study. Successful elimination of interferences was achieved in the determination of Pd, Pt and Rh mass fractions in these samples using inductively coupled plasma‐tandem mass spectrometry (ICP‐MS/MS). Based on the results, a reliable determination of Pd, Pt and Rh mass fractions in microwave‐digested moss samples was obtained using ammonia (10% NH₃ in He) in the collision/reaction cell when ¹⁰³Rh was measured either on‐mass (103→103) or with mass‐shift (103→171) and mass‐shifts for ¹⁰⁸Pd (108→159) and ¹⁹⁵Pt (195→229) were used. The ICP‐MS/MS procedure was validated using BCR‐723 (road dust) as a reference material. In addition, a good agreement between the ICP‐MS/MS results and the results obtained with cloud point extraction and quadrupole ICP‐MS was observed for the moss samples.