On the longitudinal distribution of the solar surges

After re-examination of data presented by Verma (1984), some misuse of solar parameteres published in Solar Geophysical Data is presented. Consequently some conclusions made by Verma (1984, 1986) on about the longitudinal distribution of cool solar surges based on these misuses are discussed.     

Stable isotope study of antimony deposits in the Muratdagi region,western Turkey

The Muratdagi region is rich in antimony deposits having the following common characteristics: post Miocene age, location on the down-thrown blocks next to normal faults, in the vicinity of active or fossil thermal springs, and in contact with carbonate rocks. The isotopic composition of — 7. SMOW of the mineralizing fluid calculated from the measured ° ¹⁸O of quartz and the fluid inclusion microthermometry, is indicative of meteoric water origin. The ° ¹³C of the inclusion CO₂ of — 19.1 to — 25.4 PDB is indicative of interaction with organic material-graphite. The ° ³⁴S of stibnite — 3.6 to — 0.7 is, in view of the mineral assemblage, indicative of magmatic origin of the sulphur. A tightly confined set of structural, lithological, hydrological and geochemical features define a sequence of geochemical processes; formation of acid and reducing fluid, leaching and transport of antimony complexes and precipitation of stibnite within defined lithological units. The set of processes seems to have taken place within a space of 5000 m lateral and 1000 m vertical extension.     

Geochemistry and origin of the Proterozoic ultrapotassic rocks of the Churchill Province,Canada

Summary Early Proterozoic ultrapotassic dikes, lava flows, and pyroclastic rocks of the Christopher Island Formation (CIF) erupted throughout an area 600 × 300 km within the Churchill Province of the Canadian Shield at 1.84 Ga. The rocks range from mafic lamprophyres (mg # 60; SiO₂ 47–54%, mean K₂O/Na₂O > 4) with phenocrysts of phlogopite + diopside + apatite ± olivine ± magnetite, to phenocryst-poor felsic rocks and sanidine porphyries (SiO₂55–69%). All samples have high incompatible element contents and display large depletions of high field strength elements relative to K, Rb, Sr, Ba, and Th. The CIF has geochemical and petrographic characteristics of both minettes and lamproites, but overall most closely resembles young Mediterranean lamproites. Felsic rocks of the CIF were produced by crystal fractionation and crustal contamination of mafic ultrapotassic magma, and include both high-silica lamproites strongly enriched in Zr, U, and Th, and weakly potassic to sodic rocks of trachytic composition. Flows and feeder dikes have relatively homogeneous _{Nd, 1840 Ma} (–6 to –11) but highly variable ES., 1840 Ma (–40 to + 100); samples classified as lamproites have higher average _Sr. Dike samples have highly variable present-day Pb isotope compositions, ranging from moderately to strongly nonradiogenic. Geochemical and isotopic data are consistent with contributions from depleted Archean lithospheric mantle, and OIB-type convecting mantle, both metasomatized by subduction-related processes during the Early Proterozoic. The lithospheric mantle probably contained Archean enriched domains as well. Proterozoic enrichment may have accompanied shallow underplating of subducted oceanic lithosphere beneath the Churchill Province during amalgamation of the Laurentian supercontinent. There are strong analogies in isotopic composition, and interpreted source region history, between the CIF and lamproites and minettes of the Wyoming Province and western Greenland, which suggest the existence of a Laurentian ultrapotassic superprovince.

---

Geochemie und Entstehung der Proterozoischen ultrapotassischen Gesteine der Churchill Provinz, Kanada

Zusammenfassung Altproterozoische, ultrapotassische Gänge, Lavaströme und pyroklastische Gesteine der Christopher Island Formation (CIF), eruptierten in einem Gebiet von 600 × 300 km in der Churchill Provinz des Kanadischen Schildes vor 1.84 Ga. Die Zusammensetzung dieser Gesteine variiert von mafischen Lamprophyren (mg > 60; SiO₂ = 47–54%, durchschnittliches K₂O/Na₂O > 4) mit Phänokristallent von Phlogopit + Diopsid + Apatit + Olivin + Magnetit, bis zu phänokristallarmen felsischen Gesteinen und Sanidinporphyren (SiO₂ = 55–69%). Alle Proben zeigen hohe Gehalte an inkompatiblen Elementen und zeigen beträchtliche Verarmung an high field strength Elementen relativ zu K, Rb, Sr, Ba und Th. Die CIF hat geochemische und petrographische Eigenschaften sowohl von Minetten wie von Lamproiten, aber im allgemeinen ähnelt sie am stärksten jungen mediterranen Lamproiten. Felsische Gesteine der CIF wurden durch Fraktionierung und Krustenkontamination aus mafischen ultrapotassischen Magmen gebildet. Letztere umfassen sowohl siliziumreiche Lamproite, die deutlich an Zr, U und Th angereichert sind und schwach potassische bis sodische Gesteine von trachytischer Zusammensetzung. Lavenergüsse und zufuhrgänge zeigent ein relativ homogenes _{Nd, 1840 Ma} (–6 bis –11) aber ein sehr variables _{Sr, 1840 Ma} (-40 bis + 100); Proben die als Lamproite klassifiziert wurden, zeigent höhere durchschnittliche _Sr-Werte. Proben von Gängen haben sehr variable Bleiisotopen-Zusammensetzungen, die von mäßig bis stark nichtradiogen variieren. Geochemische und Isotopendaten weisen auf Beiträge aus verarmtem archaischen lithosphärischen Mantel und aus konvektierendem OIB-Typ Mantel hin, die beide während des Alproterozoikums durch Subduktions-Vorgänge metasomatisiert wurden. Der lithosphärische Mantel enthielt wahrscheinlich auch angereicherte archaische Domänen. Proterozoische Anreicherungsvorgänge dürften seichtes Underplating subduzierter ozeanischer Lithosphäre unter der Churchill Provinz während der Amalgamation des laurentischen Superkontinentes begleitet haben. Es gibt starke Analogien in der Isotopenzusammensetzung und in der interpretierten Geschichte der Ursprungsregion, zwischen den CIF und Lamproiten und Minetten der Wyoming Provinz, und des westlichen Grönland. Diese weisen auf die Existenz einer laurentischen ultrapotassischen Superprovinz hin.

---

---

With 7 Figures     

Equation de Szebehely et principes variationnels

Resume On montre l'équivalence entre l'équation de Szebehely du problème inverse et un problème variationnel déduit du principe de Maupertuis.

---

Szebehely's equation and principle variations

We show that the inverse problem Szebehely's equations is equivalent to a multiple variation problem deduced from the principle of Maupertuis.

     

Modelling weathering processes at the catchment scale: The WITCH numerical model

A numerical model of chemical weathering in soil horizons and underlying bedrock (WITCH) has been coupled to a numerical model of water and carbon cycles in forest ecosystems (ASPECTS) to simulate the concentration of major species within the soil horizons and the stream of the Strengbach granitic watershed, located in the Vosges Mountains (France). For the first time, simulations of solute concentrations in soil layers and in the catchment river have been performed on a seasonal basis. The model is able to reproduce the concentrations of most major species within the soil horizons, as well as catching the first-order seasonal fluctuations of aqueous calcium, magnesium and silica concentrations. However, the WITCH model underestimates concentrations of Mg²⁺ and silica at the spring of the catchment stream, and significantly underestimates Ca²⁺ concentration. The deficit in calculated calcium can be compensated for by dissolution of trace apatite disseminated in the bedrock. However, the resulting increased Ca²⁺ release yields important smectite precipitation in the deepest model layer (in contact with the bedrock) and subsequent removal of large amount of silica and magnesium from solution. In contrast, the model accurately accounts for the concentrations of major species (Ca, Mg and silica) measured in the catchment stream when precipitation of clay minerals is not allowed. The model underestimation of Mg²⁺ and H₄SiO₄ concentrations when precipitation of well crystallized smectites is allowed strongly suggests that precipitation of well crystallized clay minerals is overestimated and that more soluble poorly crystallized and amorphous materials may be forming. In agreement with observations on other watersheds draining granitic rocks, this study indicates that highly soluble trace calcic phases control the aqueous calcium budget in the Strengbach watershed.     

Diagenesis and fracturing of Paleocene–Eocene carbonate turbidite systems in the Ionian Basin: The example of the Kelçyra area (Albania)

The Kelçyra area is emplaced in a foreland fold-and-thrust belt (FFTB), characterized by a westward thrusting with the Triassic evaporites as the major décollement level. Several secondary features related with this evolution, like backthrusting, folding, duplex structures, evaporite diapirism are present. During the FFTB evolution, the study area has been subjected to several fracturing events with associated stages of fluid migration. During the pre-deformational stage, complex textures such as crack-and-seal features most likely reflect expulsion of overpressured fluids. These fluids were dominantly host-rock buffered. Within the post-deformational stage, a meteoric fluid caused cementation and development of a karst network during a period of emergence after the thrust emplacement. Subsequently, Mg calcite reprecipitated in the more stable carbonate phase calcite and dolomite, which filled part of the karts network. The latter is finally dedolomitized and locally partially dissolved by a second meteoric fluid flow, which greatly increased the secondary porosity.     

Characterization and migration of atmospheric REE in soils and surface waters

Rainwater and snow collected from three different sites in France (Vosges Mountains, French Alps and Strasbourg) show more or less similar shapes of their REE distribution patterns. Rainwater from Strasbourg is the most REE enriched sample, whereas precipitations from the two mountainous, less polluted catchments are less REE enriched and have concentrations close to seawater. They are all strongly LREE depleted.Different water samples from an Alpine watershed comprising snow, interstitial, puddle and streamwater show similar REE distributions with LREE enrichment (rainwater normalized) but MREE and HREE depletion. In this environment, where water transfer from the soil to the river is very quick due to the low thickness of the soils, it appears that REE in streamwater mainly originate from atmospheric inputs. Different is the behaviour of the REE in the spring- and streamwaters from the Vosges Mountains. These waters of long residence time in the deep soil horizons react with soil and bedrock REE carrying minerals and show especially significant negative Eu anomalies compared to atmospheric inputs. Their Sr and Nd isotopic data suggest that most of the Sr and Nd originate from apatite leaching or dissolution. Soil solutions and soil leachates from the upper soil horizons due to alteration processes strongly depleted in REE carrying minerals, have REE distribution patterns close to those of lichens and throughfall. Throughfall is slightly more enriched especially in light REE than filtered rainwater probably due to leaching of atmospheric particles deposited on the foliage and also to leaf excretion.Data suggest that Sr and Nd isotopes of the soil solutions in the upper soil horizons originate from two different sources: 1) An atmospheric source with fertilizer, dust and seawater components and 2) A source mainly determined by mineral dissolution in the soil. These two different sources are also recognizable in the Sr and Nd isotopic composition of the tree’s throughfall solution. The atmospheric contributions of Sr and Nd to throughfall and soil solution are of 20 to 70 and 20%, respectively. In springwater, however, the atmospheric Sr and REE contribution is not detectable.     

An X-ray absorption fine structure and nuclear magnetic resonance spectroscopy study of gallium-silica complexes in aqueous solution

The influence of aqueous silica on gallium(III) hydrolysis in dilute (2 × 10⁻⁴ ≤ m_Ga ≤ 5 × 10⁻³) and moderately concentrated (0.02 ≤ m_Ga ≤ 0.3) aqueous solutions was studied at ambient temperature, using high resolution X-ray absorption fine structure (XAFS) and nuclear magnetic resonance (NMR) spectroscopies, respectively. Results show that, in Si-free acidic solutions (pH < 3), Ga is hexa-coordinated with oxygens of H₂O molecules and/or OH groups in the first coordination sphere of the metal. With increasing pH, these hydroxyl groups are progressively replaced by bridging oxygens (-O-), and polymerized Ga-hydroxide complexes form via Ga-O-Ga chemical bonds. In the 2.5-3.5 pH range, both XAFS and NMR spectra are consistent with the dominant presence of the Ga₁₃ Keggin polycation, which has the same local structure as A1₁₃. Under basic pH (pH > 8), Ga exhibits a tetrahedral coordination, corresponding to Ga(OH)₄⁻ species, in agreement with previous NMR and potentiometric studies. Major changes in Ga hydrolysis have been detected in the presence of aqueous silica. Ga is tetra-coordinated, both in basic and acid (i.e., at pH > 2.7) Si-bearing solutions (0.01 ≤ m_Si ≤ 0.2), and forms stable gallium-silicate complexes. In these species, Ga binds via bridging oxygen to 2 ± 1 silicons, with an average Ga-Si distance of 3.16 ± 0.05 Å, and to 2 ± 1 silicons, with an average Ga-Si distance of 3.39 ± 0.03 Å. These two sets of Ga-Si distances imply the formation of two types of Ga-silicate aqueous complex, cyclic Ga-Si_2-3 species (formed by the substitution of Si in its tri-, tetra- or hexa-cyclic polymers by Ga atoms), and chainlike GaSi_2-4 species (similar to those found for A1), respectively. The increase in the number of Si neighbors (a measure of the complex concentration and stability), in alkaline media, with increasing SiO₂(aq) content and decreasing pH is similar to that for A1-Si complexes found in neutral to basic solutions. At very acid pH and moderate silica concentrations, the presence of another type of Ga-Si complex, in which Ga remains hexa-coordinated and binds to the silicon tetrahedra via the GaO₆ octahedron corners, has also been detected. These species are similar to those found for Al³⁺ in acid solutions. Thus, as for aluminum, silicic acid greatly hampers Ga hydrolysis and enhances Ga mobility in natural waters via the formation of gallium-silicate complexes.     

Comparison between the Chile and Mexico triple junction areas substantiates slab window development beneath northwestern Mexico during the past 12-10 Myr

When combined with the Miocene-Recent volcanic record of Baja California, a parallel drawn between the Chile and Mexico triple junction areas substantiates slab window development beneath northwestern Mexico during the past 12-10 Myr. The slab-free zone manifestations challenge the notion that ridge subduction has not occurred beneath the southern Baja California peninsula. The geochemically distinctive rocks from the Santa Clara volcanic field of west-central Baja California, including coeval adakites and niobium-enriched basalt, are commonly inferred to signal partial melting of the subducting plate at shallow depths and relatively high temperatures, before slab dehydration occurs. Such PT conditions for slab melting have only been observed in association with spreading-ridge subduction. We propose that slab window development beneath southern Baja California and mainland Mexico (30° to 18°N) resulted from subduction of the East Pacific rise.     

Paléoenvironnements et caractérisation des roches mères pétrolières des séries pré-salifères du bassin intérieur du Gabon

The Interior Basin of Gabon, created during the break-up between South America and Africa, displays thick Neoproterozoic to Aptian p.p. fluvio-lacustrine deposits overlain by Aptian to Albian marine facies. Rock–Eval analyses from outcrop and drillhole samples show high content in organic matter (up to 25%) related to types I and II. These intervals are encountered within Permian, Neocomian–Barremian as well as Aptian siliciclastic succession. They constitute fairly good to excellent potential petroleum source rocks, which are most probably at the origin of oil indices recognized both in drillholes and in surface.