A new tectonic scenario for the Sanandaj–Sirjan Zone (Iran)

Recent geochemical studies of volcanic rocks forming part of the ophiolites within the Zagros and Naien-Baft orogen indicate that most of them were developed as supra-subduction ophiolites in intra-oceanic island arc environments. Intra-oceanic island arcs and ophiolites now forming the Naien-Baft zone were emplaced southwestward onto the northeastern margin of the South Sanandaj–Sirjan Zone, while those now in the High Zagros were emplaced southwestward onto the northern margin of Arabia. Thereafter, subduction continued on opposite sides of the remnant oceans. The floor of Neo-Tethys Ocean was subducted at a low angle beneath the entire Sanandaj–Sirjan Zone, and the floor of the Naien-Baft Ocean was subducted beneath the Central Iranian Micro-continent. The Naien-Baft Ocean extended into North-West Iran only temporarily. This failed ocean arm (between the Urumieh-Dokhtar Magmatic Assemblage and the main Zagros Thrust) was filled by thick Upper Triassic–Upper Jurassic sediments. The Naien-Baft Ocean finally closed in the Paleocene and Neo-Tethys closed in the Early to Middle Eocene. After Arabia was sutured to Iran, the Urumieh-Dokhtar Magmatic Assemblage recorded slab break-off in the Middle Eocene.     

Three-dimensional forward and backward modelling of diapirism: numerical approach and its applicability to the evolution of salt structures in the Pricaspian basin

Numerical studies of ductile deformations induced by salt movements have, until now, been restricted to two-dimensional (2D) modelling of diapirism. This paper suggests a numerical approach to model the evolution of three-dimensional (3D) salt structures toward increasing maturity. This approach is also used here to restore the evolution of salt structures through successive earlier stages. The numerical methodology is applied to study several model examples. We analyse a model of salt diapirs that develop from an initial random perturbation of the interface between salt and its overburden and restore the evolved salt diapirs to their initial stages. We show that the average restoration errors are less than 1%. An evolutionary model of a 2D salt wall loaded by a 2D pile of sediments predicts a decomposition of the salt wall into 3D diapiric structures when the overburden of salt is supplied by 3D synkinematic wedge of sediments. We model salt extrusion feeding a gravity current over the depositional surface and estimate an average rate of extrusion and horizontal velocity of salt spreading. Faulting of the overburden to salt overhangs initiates new secondary diapirs, and we analyse the growth of these secondary diapirs. We also study how lateral flow effects the evolution of salt diapirs. The shape of a salt diapir can be very different if the rate of horizontal flow is much greater than the initial rate of diapiric growth solely due to gravity. We discuss the applicability of the results of the models to the evolution of Late Permian salt structures in the Pricaspian basin (Russia and Kazakhstan). These structures are distinguishable into a variety of styles representing different stages of growth: salt pillows, diapirs, giant salt massifs, 2D diapiric walls and 3D stocks complicated by large overhangs. The different sizes, shapes and maturities of salt structures in different parts of the Pricaspian basin reflect areal differences in salt thickness and loading history. Our results suggest that the numerical methodology can be employed to analyse the evolution of all salt structures that have upbuilt through younger ductile overburdens.     

Phytoplankton productivity in relation to light intensity: A simple equation

A simple exponential equation is used to describe photosynthetic rate as a function of light intensity for a variety of unicellular algae and higher plants where photosynthesis is proportional to (1-e^−β1). The parameter β ( ) is derived by a simultaneous curve-fitting method, where I is incident quantum-flux density. The exponential equation is tested against a wide range of data and is found to adequately describe P vs. I curves. The errors associated with photosynthetic parameters are calculated. A simplified statistical model (Poisson) of photon capture provides a biophysical basis for the equation and for its ability to fit a range of light intensities. The exponential equation provides a non-subjective simultaneous curve fitting estimate for photosynthetic efficiency (a) which is less ambiguous than subjective methods: subjective methods assume that a linear region of the P vs. I curve is readily identifiable. Photosynthetic parameters β and a are used widely in aquatic studies to define photosynthesis at low quantum flux. These parameters are particularly important in estuarine environments where high suspended-material concentrations and high diffuse-light extinction coefficients are commonly encountered.     

Biogeography of the deep-sea galatheid squat lobsters of the Pacific Ocean

We analyzed the distribution patterns of the galatheid squat lobsters (Crustacea, Decapoda, Galatheidae) of the Pacific Ocean. We used the presence/absence data of 402 species along the continental slope and continental rise (200–2000 m) obtained from 54 cruises carried out in areas around the Philippines, Indonesia, Solomon, Vanuatu, New Caledonia, Fiji, Tonga, Wallis and Futuna and French Polynesia. The total number of stations was ca. 3200. We also used published data from other expeditions carried out in the Pacific waters, and from an exhaustive search of ca. 600 papers on the taxonomy and biogeography of Pacific species. We studied the existence of biogeographic provinces using multivariate analyses, and present data on latitudinal and longitudinal patterns of species richness, rate of endemism and the relationship between body sizes with the size of the geographic ranges. Latitudinal species richness along the Western and Eastern Pacific exhibited an increase from higher latitudes towards the Equator. Longitudinal species richness decreased considerably from the Western to the Central Pacific. Size frequency distribution for body size was strongly shifted toward small sizes and endemic species were significantly smaller than non-endemics. This study concludes that a clear separation exists between the moderately poor galatheid fauna of the Eastern Pacific and the rich Western and Central Pacific faunas. Our results also show that the highest numbers of squat lobsters are found in the Coral Sea (Solomon-Vanuatu-New Caledonia islands) and Indo-Malay-Philippines archipelago (IMPA). The distribution of endemism along the Pacific Ocean indicates that there are several major centres of diversity, e.g. Coral Sea, IMPA, New Zealand and French Polynesia. The high proportion of endemism in these areas suggests that they have evolved independently.     

Aggregate resources: Production and environmental constraints

Aggregates are produced from sand and gravel deposits or from bedrock sources. Production sites are numerous to minimize transport and are more and more in a competing land use position. Urbanization, while creating a market, also sterilizes deposits and pressures producers to relocate further from populated areas. Regulating and permitting quarries is an issue in regions with growing populations. This regulatory environment may cause exploitation schemes to evolve towards greater recycling, importing, and marine production, for example. These changes may be entirely attributable to increased environmental constraints on producing operations and not on conventional mining constraints such as overburden, ore grade, and costs of operation.     

The preservation of scleractinian corals by calcite in the corallian beds (Oxfordian) of southern England

Corals in the Oxfordian barrier-reef complex of southern England show great variations in the style and quality of preservation. Preservation was influenced by differences in the structure and chemical composition of the skeleton and by diagenetic effects such as the production of fibrous aragonite overgrowths and micrite cement. In all cases, however, the aragonite dissolved. Calcite usually precipitated in the resultant voids.

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Zusammenfassung Die Korallen des Oxford-Barriere-Riffkomplexes in Südengland unterscheiden sich wesentlich in Wuchsform und Erhaltungszustand. Der Erhaltungszustand wird durch die primären Strukturunterschiede und die chemische Zusammensetzung des Skelettes sowie durch frühdiagenetische Veränderung — wie Aragonitnadel- oder Mikrit-Zemenet — bestimmt. Der primäre Aragonit des Skelettes hat sich in jedem Fall aufgelöst, und in den dabei entstandenen Hohlräumen wird Kalzit gefällt.

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Résumé Les coraux du complexe de récif en barrière Oxfordienne d'Angleterre du sud montrent les grandes variations dans le style et la qualité de l'état de conservation. Cet état a été influencé par les différences de construction et de composition chimique du squelette et par les effets du premier stade de la diagenèse tels que la production des surcroissances de l'aragonite fibreuse et le ciment micritique. Cependant, dans tous les cas l'originale aragonite s'est dissoute, et la calcite a été précipitée dans les espaces vides résultants.

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Microbial ecology of the stratified water column of the Black Sea as revealed by a comprehensive biomarker study

The stratified water column of the Black Sea is partitioned into oxic, suboxic, and euxinic zones, each characterized by different biogeochemical processes and by distinct microbial communities. In 2003, we collected particulate matter by large volume in situ filtration at the highest resolution to date for lipid biomarker analysis and bacterioplankton for enumeration of major prokaryotic groups. Abundances of several prokaryotic groups were estimated using CARD-FISH probes specific for Bacteria, Archaea (Crenarchaeota and Euryarchaeota), epsilonproteobacteria (mainly sulfide oxidizers) and sulfate reducing bacteria. We also measured a wide range of bacterial and archaeal lipid biomarkers. Depth distributions of diagnostic biomarkers are matched with zonation of microbial processes, including aerobic bacterial oxidation of methane, oxidation of ammonium by bacteria and archaea, metal reduction, and sulfide oxidation at the chemocline, and bacterial sulfate reduction and anaerobic oxidation of methane by archaea in the anoxic zone. Cell densities for archaea and sulfate reducing bacteria are estimated based on water column biomarker concentrations and compared with CARD-FISH results.