The influence of shallow landslides on sediment supply: A flume-based investigation using sandy soil

The impact of rainfall-induced shallow landslides on hillslope sediment discharge is not well understood. This paper reports experimental measurements of sediment discharge after water-induced shallow landslides are triggered on sandy soil in a flume under simulated rainfall. The principal aim of the research was to investigate how varying soil depth affects the location and occurrence of shallow slope failures, as well as how it affects sediment yields downslope. Four experiments were conducted using the same sandy soil and a 30° and 10° compound slope configuration under average rainfall intensity of 50 mm h^− 1 for up to 390 min. Soil depths were set to 200, 300, 400 and 500 mm. Engineering and geotechnical properties of the soil were examined. Sediment discharge and runoff were collected from the flume outlet at 15 minute intervals. Changes in the soil slope profiles after landslides and soil physical properties resulted from soil armouring, under continuous rainfall were also recorded. Results showed that sediment yields at the flume outlet, before landslides occurred, were very low and limited to the finer soil particles as would be expected for a sandy soil. However subsequent variations in sediment discharge were strongly related to failure events and their proximity to the outlet. Sediment yield was also affected by the original soil depth; the greater the depth, the higher the sediment yields. Post-failure reductions in sediment discharge were observed and attributed to post-failure slope stabilization under continuing rainfall and extensive soil armouring near the flume outlet. The results provide a clear linkage between landslides and sediment discharge due to hydrological processes occurring in the hillslope. This knowledge is being used to develop a model to predict sediment discharges from hillslopes following shallow landslide events.     

An early Paleoproterozoic high-K intrusive complex in southwestern Tarim Block, NW China: Age, geochemistry, and tectonic implications

Systematic geochronologic, geochemical, and Nd isotopic analyses were carried out for an early Paleoproterozoic high-K intrusive complex exposed in southwestern Tarim, NW China. The results provide a better understanding of the Paleoproterozoic tectonic evolution of the Tarim Block. Zircon U–Pb age dating indicates two Paleoproterozoic magmatic episodes occurring at ca. 2.41 Ga and ca. 2.34 Ga respectively, which were followed by a ca. 1.9 Ga metamorphic event. The 2.41 Ga granodiorite–adamellite suite shares characteristics of late to post-orogenic metaluminous A-type granites in its high alkalinity (Na₂O + K₂O = 7.6–9.3%), total REE (410–788 ppm), Zr (370–660 ppm), and Y (21.7–58.4 ppm) contents. εNd(t) values for the suite range from − 3.22 to − 4.71 and accordingly the Nd modal ages (T_2DM) vary between 3.05 Ga and 3.17 Ga. Based on geochemical data, the 2.34 Ga suite can be subdivided into two sub-suites, namely A-type and S-type. However, both types have comparable Nd isotope compositions (εNd(t) ≈ − 0.41 to − 2.08) and similar narrow T_2DM ranges (2.76–2.91 Ga).Geochemical and Nd isotopic data for the high-K intrusive complex, in conjunction with the regional geological setting, suggest that both the 2.41 Ga suite and the 2.34 Ga A-type sub-suite might have been produced by partial melting of the Archean mafic crust in a continental rift environment. The S-type sub-suite is thought to have formed by partial melting of felsic pelites and/or metagreywackes recycled from Archean crust (TTG?). Gabbro enclaves with positive εNd(t) value (2.15) have been found to be intermingling within the 2.34 Ga suite; ca. 2.34–2.36 Ga gabbroic dykes and adamellites have previously been documented in eastern Tarim. These observations indicate that the high-K intrusions may reflect the emergence of depleted mantle upwelling beneath the Tarim Block at that time. We suggest a three-stages model for the Precambrian crustal evolution in the Tarim Block: (1) the formation of proto-crust (TTG) by ca. 2.5 Ga, (2) episodes of felsic magmatism possibly occurring in continental rift environments at ca. 2.41 Ga and ca. 2.34–2.36 Ga, and (3) ca. 1.9 Ga metamorphism that may represent the solidification of the Precambrian basement of the Tarim Block.     

Quantitative reconstruction of Holocene precipitation changes in southern Patagonia

Holocene variations in annual precipitation (P_ann) were reconstructed from pollen data from southern Argentinian Patagonia using a transfer function developed based on a weighted-averaging partial least squares (WA-PLS) regression. The pollen–climate calibration model consisted of 112 surface soil samples and 59 pollen types from the main vegetation units, and modern precipitation values obtained from a global climate database. The performance (r² = 0.517; RMSEP = 126 mm) of the model was comparable or slightly lower than in other comparable pollen–climate models. Fossil pollen data were obtained from a sediment core from Cerro Frias site (50°24'S, 72°42'W) located at the forest-steppe ecotone. Reconstructed P_ann values of about 200 mm suggest dry conditions during the Pleistocene–Holocene transition (12,500–10,500 cal yr BP). P_ann values were about 300–350 mm from 10,500 to 8000 cal yr BP and increased to 400–500 mm between 8000 and 1000 cal yr BP. An abrupt decrease in P_ann at about 1000 cal yr BP was associated with a Nothofagus decline. The reconstructed P_ann suggests a weakening and southward shift of the westerlies during the early Holocene and intensification, with no major latitudinal shifts, during the mid-Holocene at high latitudes in southern Patagonia.     

Geometry of the fault zone of the 2003 Ms = 7.5 Chuya earthquake and associated stress fields, Gorny Altai

The co-seismic deformations produced during the September 27, 2003 Chuya earthquake (Ms = 7.5) that affected the Gorny Altai, Russia, are described and discussed along a 30 km long segment. The co-seismic deformations have manifested themselves both in unconsolidated sediments as R- and R′-shears, extension fractures and contraction structures, and in bedrock as the reactivation of preexisting schistosity zones and individual fractures, as well as development of new ruptures and coarse crushing zones. It has been established that the pattern of earthquake ruptures represents a typical fault zone trending NW–SE with a width reaching 4–5 km and a dextral strike–slip kinematics. The initial stress field that produced the whole structural pattern of co-seismic deformations during the Chuya earthquake, is associated with a transcurrent regime with a NNW–SSE, almost N–S, trending of compressional stress axis (σ₁), and a ENE–WSW, almost E–W, trending of tensional stress axis (σ₃). The state of stress in the newly-formed fault zone is relatively uniform. The local stress variations are expressed in insignificant deviation of σ₁ from N–S to NW–SE or NE–SW, in short-term fluctuations of relative stress values in keeping their spatial orientations, or in a local increase of the plunge angle of the σ₁. The geometry of the fault zone associated with the Chuya earthquake has been compared with the mechanical model of fracturing in large continental fault zones with dextral strike–slip kinematics. It is apparent that the observed fracture pattern corresponds to the late disjunctive stage of faulting when the master fault is not fully developed but its segments are already clearly defined. It has been shown that fracturing in widely different rocks follows the common laws of the deformation of solid bodies, even close to the Earth surface, and with high rates of movements.     

Permian–Jurassic Mahanadi and Pranhita–Godavari Rifts of Gondwana India: Provenance from regional paleoslope and U–Pb/Hf analysis of detrital zircons

The Permian–Jurassic Mahanadi and Pranhita–Godavari Rifts are part of a drainage system that radiated from the Gamburtsev Subglacial Mountains in central Antarctica. From 12 samples we analysed detrital zircons for U–Pb ages, Hf-isotopes, and trace elements to determine the age, rock type and source of the host magma, and T_DM model age. Clusters, in decreasing order of abundance, are (1) 820–1000 Ma, host magmas felsic granitoids with alkaline rock, (2) 1500–1700 Ma felsic granitoids, (3) 500 to 700 Ma mafic granitoids with alkaline rock, (4) 2400–2550 Ma granitoids, and (5) 1000–1200 Ma felsic and mafic granitoids, mafic rock, and alkaline rock. T_DM ranges from 1.5 to 3.5 Ga. Joint paleoslope measurements and zircon ages indicate that the Eastern Ghats Mobile Belt (EGMB) and lateral belts and conjugate Antarctica are potential provenances. Zircons from the Gondwana Rifts differ from those in other Gondwanaland sandstones in their predominant 820–1000 Ma and 1500–1700 Ma ages (from the EGMB and conjugate Rayner–MacRobertson Belt) that dilute the 500–700 Ma (Pan-Gondwanaland) ages. The 1000–1200 Ma zircons reflect the assembly of Rodinia, the 500–700 Ma ones that of Gondwanaland; the other ages reflect collisions in the region.     

Geochronological problems related to polymetamorphism in the Limpopo Complex, South Africa

The integration of new and published geochronologic data with structural, magmatic/anatectic and pressure–temperature (P–T) process information allow the recognition of high-grade polymetamorphic granulites and associated high-grade shear zones in the Central Zone (CZ) of the Limpopo high-grade terrain in South Africa. Together, these two important features reflect a major high-grade D₃/M₃ event at ~ 2.02 Ga that overprinted the > 2.63 Ga high-grade Neoarchaean D₂/M₂ event, characterized by SW-plunging sheath folds. These major D₂/M₂ folds developed before ~ 2.63 Ga based on U–Pb zircon age data for precursors to leucocratic anatectic gneisses that cut the high-grade gneissic fabric. The D₃/M₃ shear event is accurately dated by U–Pb monazite (2017.1 ± 2.8 Ma) and PbSL garnet (2023 ± 11 Ma) age data obtained from syntectonic anatectic material, and from sheared metapelitic gneisses that were completely reworked during the high-grade shear event. The shear event was preceded by isobaric heating (P = ~ 6 kbar and T = ~ 670–780 °C), which resulted in the widespread formation of polymetamorphic granulites. Many efforts to date high-grade gneisses from the CZ using PbSL garnet dating resulted in a large spread of ages (~ 2.0–2.6 Ga) that reflect the polymetamorphic nature of these complexly deformed high-grade rocks.     

Geochemistry and stable isotopic composition of tufa waters and precipitates from the Interlake Region, Manitoba, Canada: Constraints on groundwater origin, calcitization, and tufa formation

New major, trace and isotopic geochemical results from a regional study of springs discharging from the major carbonate rock aquifer in the Interlake Region of Manitoba, Canada, are used to understand water–rock reactions, timing of recharge/discharge, tufa formation processes, and as baseline data. Spring waters are fresh with total dissolved solids (TDS) concentrations ranging from 150 to 880 mg/L. Waters discharging in the northern part of the study area have lower TDS, are dominantly Ca–Mg–HCO₃ waters with low SO₄ concentrations (<< 50 mg/L), and appear to have interacted primarily with Silurian carbonate lithologies. In contrast, waters in the southeastern part of the study area have higher TDS and have elevated SO₄ concentrations (up to 210 mg/L). Spring waters have elevated Mg/Ca_molar (1.23 ± 0.23), typically greater than congruent dissolution of dolomite. Ca and Mg concentrations and Mg/Ca_molar indicate that groundwater residence times were sufficient to allow equilibration with bedrock dolomite lithologies; elevated tritium in northern waters indicates a significant recharge component in the 1960's and 1970's. Tufa precipitates that have formed from many of the spring waters are low-Mg calcite (MgO = 1.70 to 5.80 wt.%). Sr concentrations are variable (57 to 657 ppm) and tufa Sr/Ca_molar ratios appear to be entirely controlled by spring water Sr/Ca_molar. Empirically determined Sr distribution coefficients (D_Sr = 0.389 ± 0.083) indicate rapid crystallization following CO₂ degassing, consistent with heavier δ¹³C_VPDB compared to spring waters. Sulfate concentrations are generally too low for calcitization (dedolomitization) reactions driven by anhydrite dissolution to be the dominant control on the elevated groundwater Mg/Ca_molar, implying either extensive sulfate reduction along the flow paths (however, δ¹³C_DIC suggests the elevated SO₄ is more consistent with Fe-sulfide oxidation), or that other processes are involved. Major ion ratios suggest that the waters in the southern part of the study area are more consistent with interaction with siliciclastic rocks than with anhydrite dissolution. We suggest that calcitization (dedolomitization) reactions driven by anhydrite dissolution may not dominate all carbonate aquifers and that mixing of waters in karst conduits combined with ion exchange reactions are important controls on water chemistry in these systems.     

HP–LT Variscan metamorphism in the Cubito-Moura schists (Ossa-Morena Zone, southern Iberia)

Multi-equilibrium thermobarometry shows that low-grade metapelites (Cubito-Moura schists) from the Ossa–Morena Zone underwent HP–LT metamorphism from 340–370 °C at 1.0–0.9 GPa to 400–450 °C at 0.8–0.7 GPa. These HP–LT equilibriums were reached by parageneses including white K mica, chlorite and chloritoid, which define the earliest schistosity (S₁) in these rocks. The main foliation in the schists is a crenulation cleavage (S₂), which developed during decompression from 0.8–0.7 to 0.4–0.3 GPa at increasing temperatures from 400–450 °C to 440–465 °C. Fe³⁺ in chlorite decreased greatly during prograde metamorphism from molar fractions of 0.4 determined in syn-S₁ chlorites down to 0.1 in syn-S₂ chlorites. These new data add to previous findings of eclogites in the Moura schists indicating that a pile of allochtonous rocks situated next to the Beja-Acebuches oceanic amphibolites underwent HP–LT metamorphism during the Variscan orogeny. To cite this article: G. Booth-Rea et al., C. R. Geoscience 338 (2006).     

Solid inclusions of magmatic halite and sylvite in felsic granitoids, Sierra Norte, Córdoba, Argentina

This study provides evidence for the existence of halite and sylvite solid inclusions in igneous quartz and feldspars, the first to be reported in intrusive rocks, and to partially constrain the physicochemical environment that lets halides crystallize under magmatic conditions.Halite and sylvite solid inclusions were found included in quartz and feldspars from a micrographic–granophyric assemblage in a miarolitic aplite and, rarer, in alkali-feldspar from a miarolitic monzogranite. Monzogranite and aplite represent I-type, K-enriched postcollisional rocks of the Late Cambrian–Early Ordovician Sierra Norte–Ambargasta batholith in the Eastern Sierras Pampeanas. Both granitoids fall among the most evolved felsic rocks of the batholith, with aplite approaching haplogranitic compositions. Halite is far more common than sylvite and the presence and distribution of one or both halides are erratic within the felsic intrusive bodies. Halides occur as small skeletal grains, commonly in cross-shaped aggregates of less than 50 μm. No K or Na was found at the detection limits of EDS in either halite or sylvite respectively. Textural relationships suggest that the alkali-chlorides separated from the melt near the minima along the quartz–feldspar cotectics of P_H2O > 160 < 200 MPa in a silica-, and potassium-rich magmatic system at approximately 750–700 °C, prior to the H₂O-vapor saturated miarole-forming stage.Computed ratios for the magmatic volatile phase (MVP) coexisting with melt at the early stage of aplite crystallization are: NaCl/HCl = 0.11–0.97 and KCl/HCl = 0.24–1.62, being the highest range of values (0.79–0.97 and 1.45–1.62, respectively) found in those alkali-chloride-bearing samples. Maximum HCl/ΣCl_(MVP) (0.28 to 0.31) indicates higher total Cl concentration in the MVP of alkali-chloride-bearing aplites, which is much higher in the halite-free aplite samples (HCl/ΣCl_(MVP) = 0.59 to 0.74). One miarolitic monzogranite sample, where halite solid inclusions are present, also yielded the highest ratios for NaCl/HCl_(MVP) (0.91) and KCl/HCl_(MVP) (1.46), and the HCl/ΣCl_(MVP) is 0.30. A high HCl concentration in the fluid phase is suggested by the log f(HF)/f(H₂O) = − 4.75 to − 4.95, log f(HCl)/f(H₂O) = − 3.73 to − 3.86, and log f(HF)/f(HCl) = − 0.88 to − 1.22, computed at 750 °C after biotite composition. The Cl concentrations at 800 °C, computed with a D^v/l_Cl = 0.84 + 26.6P (P at 200 MPa), yielded values within the range of  70 to 700 ppm Cl in the melt and  4000 to 40 000 ppm Cl in the coexisting MVP. The preferential partitioning of Cl in the vapor phase is controlled by the D^v/l_Cl; however, the low concentration of Cl in the melt suggests that high concentrations of Cl are not necessary to saturate the melt in NaCl or KCl.Cl-saturation of the melt and coexisting MVP might have been produced by a drop in Cl solubility due to the near-haplogranitic composition of the granitoids after extreme fractionation, probably enhanced by fluctuating reductions of the emplacement pressure in the brittle monzogranite host. Liquid immiscibility, based in the differential viscosity and density among alkali-chloride saturated hydrosaline melt, aluminosilicate felsic melt, and H₂O-rich volatiles is likely to have crystallized halite and sylvite from exsolved hydrosaline melt. High degrees of undercooling might have been important at the time of alkali-chloride exsolution. The effectiveness of alkali-chloride separation from the melt at magmatic temperatures is in line with the interpretation of “halite subtraction” as a necessary process to understand the origin of the “halite trend” in highly saline fluid inclusions from porphyry copper and other hydrothermal mineralizations, despite the absence of the latter in the Cerro Baritina aplites, where this process preceded the exsolution of halite-undersaturated fluids.Pervasive alteration of the monzogranite country rock as alkali-metasomatic mineral assemblages, the mineral chemistry of some species, and the association of weak molybdenite mineralization are compatible with the activity of alkaline hypersaline fluids, most likely exsolved during the earliest stages of aplite consolidation.     

Dissolved air flotation (DAF) of fine quartz particles using an amine as collector

Experimental studies concerning the dissolved air flotation (DAF) of fine (d_p < 100 μm) quartz particles, using two different flotation cells (setups), are presented. Pure and well characterised quartz samples were treated with a commercial amine as collector prior to flotation and bubbles were characterised by the LTM-BSizer technique. Bubble size distribution showed 71% (by volume) and 94% (by number) of the bubbles having sizes (d_b) lower than 100 μm (i.e. microbubbles). The Sauter and arithmetic mean diameters were 79 μm and 56 μm, respectively, for the bubbles generated at 300 kPa (gauge) saturation pressure (after 30 minute saturation time). Quartz particle size distribution (obtained by laser diffraction) showed a volume-moment diameter of 13 μm. The Rosin–Rammler–Bennett, Gates–Gaudin–Schumann and log-normal distribution functions were well fitted (R² > 0.96) to the bubble size distribution and quartz particle size distribution data. Values of total quartz recovery ranging from 6% to 53% (by mass) were obtained for the DAF experiments under different collector concentrations (up to 2 mg g^− 1), with an optimal collector concentration found at 1 mg g^− 1. These results are significant considering that 27% (by volume) of the quartz particles are ultrafine (d_p < 5 μm), demonstrating the widely-known efficiency of DAF to remove small particles when applied in the field of water and wastewater treatment. The true flotation behaviour, as a function of particle diameter (d_p), exhibits a local minimum when particles are approximately 3–5 μm in size. The results contribute to the discussion in the literature about the existence of such a minimum, which is generally interpreted as a change in the mechanism of particle collection from convection (collision) to diffusion at lower particle sizes.     

Mineral assemblages of the Francisco I. Madero Zn–Cu–Pb–(Ag) deposit, Zacatecas, Mexico: Implications for ore deposit genesis

The Francisco I. Madero deposit, central Mexico, occurs in the Mesozoic Guerrero Terrane, which hosts many ore deposits, both Cretaceous (volcanogenic massive sulfides) and Tertiary (epithermal and skarn deposits). It is hosted by a 600 m-thick calcareous-pelitic unit, of Lower Cretaceous age, crosscut by porphyritic dikes that strike NW–SE. A thick felsic volcanic Tertiary sequence, consisting of andesites and rhyolitic ignimbrites, unconformably overlies the Cretaceous series. At the base, the mineralization consists of several mantos developed within calcareous beds. They are dominantly composed of sphalerite, pyrrhotite and pyrite with minor chalcopyrite, arsenopyrite and galena. At the top of the orebody, there are calcic skarns formed through prograde and retrograde stages. The resulting mineral assemblages are rich in manganoan hedenbergite (Hd_75–28Di_40–4Jh_40–20), andraditic garnets (Adr_100–62Grs_38–0), epidote (Ep_95–36Czo_60–5Pie_8–0), chamosite, calcite and quartz. The temperature of ore deposition, estimated by chlorite and arsenopyrite geothermometry, ranges from 243° to 277 °C and from 300° to 340 °C, respectively. The pressure estimated from sphalerite geobarometry averages 2.1 kbar. This value corresponds to a moderately deep skarn and agrees with the high Cu content of the deposit. Paragenesis, P–T conditions and geological characteristics are compatible with a distal, dike-related, Zn skarn deposit. Its style of mineralization is similar to that of many high-temperature carbonate replacement skarn deposits in the Southern Cordillera.     

Lowland rainforest response to hydrological changes during the last 1500 years in Gabon, Western Equatorial Africa

Pollen and δ¹³C_TOM data obtained from two contrasting lake sequences (Lakes Kamalété and Nguène), located 200 km apart in the lowland rainforest of Gabon, provide complementary local and regional 1500-yr records of high resolution (15–30 yr) vegetation change. A combination of aquatic, semi-aquatic and terrestrial pollen showed in both records that the tropical rainforest increased during periods of high rainfall and decreased during drought intervals. The strong fluctuations of water balance at decadal scale during the “Medieval Warm Period” ( 1100–800 cal yr BP) coincided with a noticeable increase in shade-intolerant taxa, indicating recurring rainforest canopy disturbance. The δ¹³C_TOM signal showed high-amplitude variations in both records, which positively correlates with the rainforest dynamics and local vegetation changes. The similar trends in both the pollen and the δ¹³C_TOM signals between these sites demonstrate the regional broadly synchronous timing of shifting hydrological conditions. The largely positive co-variation between strong fluctuations of hydrological conditions and changes in rainforest structure and composition indicate that regional climatic change is probably the driving force for major rainforest dynamics in Gabon. Any significant anthropogenic impact on vegetation has not been clearly identified, and this issue still needs to be resolved independently by obtaining detailed archeological records across the interval 1400–800 BP, which currently seem to be extremely rare or not easily available.     

Organic geochemistry and petrology of barren and Mo–Ni–PGE mineralized marine black shales of the Lower Cambrian Niutitang Formation (South China)

Marine black shales of the Lower Cambrian Niutitang Formation in southern China host Mo–Ni–platinum group elements (PGE) mineralization confined to a phosphate- and pyrite-rich stratiform body (max. 20-cm thick). The H/C atomic ratio, carbon isotopic composition, FTIR spectra of bulk organic matter, and spectra of extractable part of organic matter indicate similar sources and thermal evolution of organic matter in barren and mineralized black shales.The morphology and relative abundance of organic particles in barren and mineralized shales are different. In barren black shales, organic particles comprise only elongated bodies and laminae 2–10 μm across or elongated larger bodies (> 10 μm) with R_max = 2.96–5.21% (Type I particles). Mineralized black shales contain Type I particles in rock matrix (90–95 vol%), small veinlets or irregular organic accumulations (Type II particles, 1–5 vol%) that display weak to well developed mosaic texture and a variable reflectance (R_max = 3.55–8.65%), and small (< 1 to 5 μm) rounded or irregular Type III organic particles (1–4 vol%) distributed within phosphate nodules and sulphide rip-up clasts. Type III particles show similar reflectance as particles of Type I in rock matrix. Type I particles are interpreted as remnants of in situ bacterially reworked organic matter of cyanobacteria/algal type, Type II as solidified products or oil-derived material (migrabitumen), and Type III particles as remnants of original organic matter in phosphatized or sulphidized algal/microbial oncolite-like bodies. Equivalent vitrinite reflectances of Type I and III particles in barren and mineralized rocks are similar and correspond to semi-anthracite and anthracite. Micro-Raman spectra of organic particles in rocks display a wide belt in the area of 1600 cm^− 1 (G belt) and approximately the same belt in the area of 1350 cm^− 1 (D belt). The ratio of integrated areas of the two belts correlate with R_max values.The Mo–Ni–PGE mineralized body is interpreted as to represent a remnant of phosphate- and sulphide-rich subaquatic hardground supplied with organic material derived from plankton and benthic communities as well as with algal/microbial oncolite-like bodies that originated in wave-agitated, shallow-water, nearshore environment.     

Stress state analysis of a collapsed overhanging rock slab: A case study

This paper describes the geomechanical back-analysis of the flexural failure of an overhanging limestone slab (volume = 68 m³) that collapsed on 26/01/1999 on the abandoned Cellina Valley state road SS 251 (western Friuli, NE Italy). The survey carried out on site examining the contact surfaces between the block and the slope has ascertained that the rock slab was connected to the stable rock mass by means of a single great rock bridge. The detailed reconstruction of the slab geometry and of the actual restraint conditions acting before the rockfall permitted an estimation of the stress state by using a 3D finite element code (Strand7). The finite element numerical model, referred to the restrained cross-section measured on site (A_res = 2.82 m²), gives a maximum value of σ_t = 5.19 MPa for the tensile stress, which is in good agreement with the estimated value for the characteristic strength mobilized at rupture by the intact rock material (T₀ = 3.5–5.5 MPa). Considerably lower maximum tensile stress (σ_t = 2.25 MPa), smaller than one half, is obtained if the whole contact surface is assumed as resisting surface (A_res = 10.50 m²) and the rock bridge is neglected.     

Comparison of methods for the estimation of pyrite oxidation rate in a waste rock pile at Mine Doyon site, Quebec, Canada

Several methods were evaluated and compared for the estimation of pyrite oxidation rates (POR) in waste rock at Mine Doyon, Quebec, Canada. Methods based on data collected in situ, such as the interpretation of temperature and oxygen concentration profiles (TOP) measured in the waste rock pile and pyrite mass balance (PMB) on solid phase samples were compared with the oxygen consumption measurements (OCM) in closed chamber in the laboratory. A 1-D analytical solution to a gas and heat transport equation used temperature and oxygen profiles (TOP) measured in the pile for the preliminary POR estimates at a site close to the slope of the pile (Site 6) and in the core of the pile (Site 7). Resulting POR values were 1.1 × 10^− 9 mol(O₂) kg^− 1 s^− 1 and 1.0 × 10^− 10 mol(O₂) kg^− 1 s^− 1 for the slope site and the core site, respectively. Oxidation rates based on pyrite mass balance (PMB) calculations for solid samples were 2.21 × 10^− 9 mol(O₂) kg^− 1 s^− 1 and 2.03 × 10^− 9 mol(O₂) kg^− 1 s^− 1, respectively, for the same slope and core sites, but the difference between sites was within the error margin. The OCM measurements in the laboratory on fresh waste rock samples yielded higher POR values than field methods, with average oxidation rate of 6.7 × 10^− 8 mol(O₂) kg^− 1 s^− 1. However, the OCM results on weathered and decomposed material from the rock stockpile (average oxidation rate 3.4 × 10^− 9 mol(O₂) kg^− 1 s^− 1) were consistent with results from the field-based estimates. When POR values based on fresh material are excluded, the remaining POR values for all methods range from 1.0 × 10^− 10 to 3.4 × 10^− 9 mol(O₂) kg^− 1 s^− 1. The lowest estimated value (1.0 × 10^− 10 mol(O₂) kg^− 1 s^− 1) was based on TOP estimates in the interior of the pile where oxygen transport was limited by diffusion from the surface. These results suggest that small-scale OCM laboratory experiments may provide relatively representative values of POR in the zones of waste rock piles in which oxygen transport is not dominated by diffusion.     

Petrology and CHIME geochronology of Pan-African high K and Sr/Y granitoids in the Nkambe area, Cameroon

The Central African Belt in the Nkambe area, northwestern Cameroon represents a collisional zone between the Saharan metacraton and the Congo craton during the Pan-African orogeny, and exposes a variety of granitoids including foliated and massive biotite monzogranites in syn- and post-kinematic settings. Foliated and massive biotite monzogranites have almost identical high-K calc-alkaline compositions, with 73–67 wt.% SiO₂, 17–13 wt.% Al₂O₃, 2.1–0.9 wt.% CaO, 4.4–2.7 wt.% Na₂O and 6.3–4.4 wt.% K₂O. High concentrations of Rb (264–96 ppm), Sr (976–117 ppm), Ba (3680–490 ppm) and Zr (494–99 ppm), with low concentrations of Y (mostly< 20 ppm with a range 54–6) and Nb (up to 24 ppm) suggest that the monzogranites intruded in collisional and post-collisional settings. The Sr/Y ratio ranges from 25 to 89. K, Rb and Ba resided in a single major phase such as K-feldspar in the source. Garnet was present in the source and remained as restite at the site of magma generation. This high K₂O and Sr/Y granitic magma was generated by partial melting of a granitic protolith under high-pressure and H₂O undersaturated conditions where garnet coexists with K-feldspar, albitic plagioclase. CHIME (chemical Th–U-total Pb isochron method) dating of zircon yields ages of 569 ± 12–558 ± 24 Ma for the foliated biotite monzogranite and 533 ± 12–524 ± 28 Ma for the massive biotite monzogranite indicating that the collision forming the Central African Belt continued in to Ediacaran (ca 560 Ma).     

Tracing high-pressure metamorphism in marbles: Phase relations in high-grade aluminous calcite–dolomite marbles from the Greek Rhodope massif in the system CaO–MgO–Al2O3–SiO2–CO2 and indications of prior aragonite

Four different types of parageneses of the minerals calcite, dolomite, diopside, forsterite, spinel, amphibole (pargasite), (Ti–)clinohumite and phlogopite were observed in calcite–dolomite marbles collected in the Kimi-Complex of the Rhodope Metamorphic Province (RMP). The presence of former aragonite can be inferred from carbonate inclusions, which, in combination with an analysis of phase relations in the simplified system CaO–MgO–Al₂O₃–SiO₂–CO₂ (CMAS–CO₂) show that the mineral assemblages preserved in these marbles most likely equilibrated at the aragonite–calcite transition, slightly below the coesite stability field, at ca. 720 °C, 25 kbar and a_CO2 ~ 0.01. The thermodynamic model predicts that no matter what activity of CO₂, garnet has to be present in aluminous calcite–dolomite-marble at UHP conditions.     

The structure of the lower crust at the Argentine continental margin, South Atlantic at 44°S

It is well established that the Argentine passive margin is of the rifted volcanic margin type. This classification is based primarily on the presence of a buried volcanic wedge beneath the continental slope, manifested by seismic data as a seaward dipping reflector sequence (SDRS). Here, we investigate the deep structure of the Argentine volcanic margin at 44°S over 200 km from the shelf to the deep oceanic Argentine Basin. We use wide-angle reflection/refraction seismic data to perform a joint travel time inversion for refracted and reflected travel times. The resulting P-wave velocity-depth model confirms the typical volcanic margin structure. An underplated body is resolved as distinctive high seismic velocity (v_p up to 7.5 km/s) feature in the lower crust in the prolongation of a seaward dipping reflector sequence. A remarkable result is that a second, isolated body of high seismic velocity (v_p up to 7.3 km/s) exists landward of the first high-velocity feature. The centres of both bodies are 60 km apart. The high-velocity lower-crustal bodies likely were emplaced during transient magmatic–volcanic events accompanying the late rifting and initial drifting stages. The lateral variability of the lower crust may be an expression of a multiple rifting process in the sense that the South Atlantic rift evolved by instantaneous breakup of longer continental margin segments. These segments are confined by transfer zones that acted as rift propagation barriers. A lower-crustal reflector was detected at 3 to 5 km above the modern Moho and probably represents the lower boundary of stretched continental crust. With this finding we suggest that the continent–ocean boundary is situated 70 km more seaward than in previous interpretations.     

Thermodynamic properties of hematite — ilmenite — geikielite solid solutions

A solution model is developed for rhombohedral oxide solid solutions having compositions within the ternary system ilmenite [(Fe ₂₊ ^s Ti ₄₊ ^1–s ) ^A (Fe ₂₊ ^1–s Ti ₄₊ ^s ) ^B O₃]-geikielite [(Mg ₂₊ ^t Ti ₄₊ ^1–t ) ^A (Mg ₂₊ ^1–t Ti ₄₊ ^t ) ^B O₃]-hematite [(Fe³⁺) ^A (Fe³⁺) ^B O₃]. The model incorporates an expression for the configurational entropy of solution, which accounts for varying degrees of structural long-range order (0s, t1) and utilizes simple regular solution theory to characterize the excess Gibbs free energy of mixing within the five-dimensional composition-ordering space. The 13 model parameters are calibrated from available data on: (1) the degree of long-range order and the composition-temperature dependence of the transition along the ilmenite-hematite binary join; (2) the compositions of coexisting olivine and rhombohedral oxide solid solutions close to the Mg–Fe²⁺ join; (3) the shape of the miscibility gap along the ilmenite-hematite join; (4) the compositions of coexisting spinel and rhombohedral oxide solid solutions along the Fe²⁺–Fe³⁺ join. In the course of calibration, estimates are obtained for the reference state enthalpy of formation of ulvöspinel and stoichiometric hematite (–1488.5 and –822.0 kJ/mol at 298 K and 1 bar, respectively). The model involves no excess entropies of mixing nor does it incorporate ternary interaction parameters. The formulation fits the available data and represents an internally consistent energetic model when used in conjuction with the standard state thermodynamic data set of Berman (1988) and the solution theory for orthopyroxenes, olivines and Fe–Mg titanomagnetite-aluminate-chromate spinels developed by Sack and Ghiorso (1989, 1990a, b). Calculated activity-composition relations for the end-members of the series, demonstrate the substantial degree of nonideality associated with interactions between the ordered and disordered structures and the dominant influence of the miscibility gap across much of the ternary system. The predicted shape of the miscibility gap, and the orientation of tie-lines relating the compositions of coexisting phases, display the effects of coupling between the excess enthalpy of solution and the degree of long-range order. One limb of the miscibility gap follows the composititiontemperature surface corresponding to the ternary second-order transition.