Abiotic formation of hydrocarbons under hydrothermal conditions: Constraints from chemical and isotope data

To understand reaction pathways and isotope systematics during mineral-catalyzed abiotic synthesis of hydrocarbons under hydrothermal conditions, experiments involving magnetite and CO₂ and H₂-bearing aqueous fluids were conducted at 400 °C and 500 bars. A robust technique for sample storage and transfer from experimental apparatus to stable isotope mass spectrometer provides a methodology for integration of both carbon and hydrogen isotope characterization of reactants and products generated during abiogenic synthesis experiments. Experiments were performed with and without pretreatment of magnetite to remove background carbon associated with the mineral catalyst. Prior to experiments, the abundance and carbon isotope composition of all carbon-bearing components were determined. Time-series samples of the fluid from all experiments indicated significant concentrations of dissolved CO and C₁-C₃ hydrocarbons and relatively large changes in dissolved CO₂ and H₂ concentrations, consistent with formation of additional hydrocarbon components beyond C₃. The existence of relatively high dissolved alkanes in the experiment involving non-pretreated magnetite in particular, suggests a complex catalytic process, likely involving reinforcing effects of mineral-derived carbon with newly synthesized hydrocarbons at the magnetite surface. Similar reactions may be important mechanisms for carbon reduction in chemically complex natural hydrothermal systems. In spite of evidence supporting abiotic hydrocarbon formation in all experiments, an “isotopic reversal” trend was not observed for ¹³C values of dissolved alkanes with increasing carbon number. This may relate to the specific mechanism of carbon reduction and hydrocarbon chain growth under hydrothermal conditions at elevated temperatures and pressures. Over time, significant ¹³C depletion in CH₄ suggests either depolymerization reactions occurring in addition to synthesis, or reactions between the C₁-C₃ hydrocarbons and carbon species absorbed on mineral surfaces and in solution.     

A search for double-peaked narrow emission line galaxies and AGNs in the LAMOST DR1

The Large Sky Area Multi-Object Fiber Spectroscopic Telescope(LAMOST) has released more than two million spectra,which provide the opportunity to search for double-peaked narrow emission line(NEL) galaxies and active galactic nuclei(AGNs).The double-peaked narrow-line profiles can be well modeled by two velocity components,respectively blueshifted and redshifted with respect to the systemic recession velocity.This paper presents 20 double-peaked NEL galaxies and AGNs found from LAMOST DR1 using a search method based on a multi-Gaussian fit of the narrow emission lines.Among them,ten have already been published by other authors,either listed as genuine double-peaked NEL objects or as asymmetric NEL objects,and the remaining ten are original discoveries.We discuss some possible origins for the double-peaked narrow-line features,such as interaction between jet and narrow line regions,interaction with companion galaxies,and black hole binaries.Spatially resolved optical imaging and/or follow-up observations in other spectral bands are needed to further discuss the physical mechanisms at work.     

Environmental mineralogy – Understanding element behavior in ecosystems

Environmental Mineralogy has developed over the past decade in response to the recognition that minerals are linked in many important ways with the global ecosystem. Minerals are the main repositories of the chemical elements in Earth's crust and thus are the main sources of elements needed for the development of civilization, contaminant and pollutant elements that impact global and local ecosystems, and elements that are essential plant nutrients. These elements are released from minerals through natural processes, such as chemical weathering, and anthropogenic activities, such as mining and energy production, agriculture and industrial activities, and careless waste disposal. Minerals also play key roles in the biogeochemical cycling of the elements, sequestering elements and releasing them as the primary minerals in crustal rocks undergo various structural and compositional transformations in response to physical, chemical, and biological processes that produce secondary minerals and soils. These processes have resulted in the release of toxic elements such as arsenic in groundwater aquifers, which is having a major impact on the health of millions of people in South and Southeast Asia. The interfaces between mineral surfaces and aqueous solutions are the locations of most chemical reactions that control the composition of the natural environment, including the composition of natural waters. The nuclear fuel cycle, from uranium mining to the disposition of high-level nuclear waste, is also intimately related to minerals. A fundamental understanding of these processes requires molecular-scale information about minerals, their bulk structures and properties such as solubility, their surfaces, and their interactions with aqueous solutions, atmospheric and soil gases, natural organic matter, and biological organisms. Gaining this understanding is further complicated by the presence of natural, incidental, and manufactured nanoparticles in the environment, which are becoming increasingly important due to the rapidly developing field of nanotechnology. As a result of this complexity, Environmental Mineralogy requires the use of the most modern molecular-scale analytical and theoretical methods and overlaps substantially with closely related fields such as Environmental Sciences, low-temperature Geochemistry, and Geomicrobiology. This paper provides brief overviews of the above topics and discusses the complexity of minerals, natural vs. anthropogenic inputs of elements and pollutants into the biosphere, the role of minerals in the biogeochemical cycling of elements, natural nanoparticles, and the Environmental Mineralogy of three major potential pollutant elements (Hg, As and U).     

Variation and temporal patterns in the composition of the surface ichthyoplankton in the southern Bay of Biscay (W. Atlantic)

From September 2000 to December 2006, surface plankton samples were collected on a monthly basis, from a station located in the southern Bay of Biscay (43°37N; 1°43W France), near the deep Capbreton canyon. In this paper, the results for the ichthyoplankton assemblage are presented. Among the 62 taxa recorded, only 35 were present in the larval stage whilst only 10 were represented by their eggs. Taxa represented by both stages (eggs+larvae; N=17) had the highest abundance. The presence in the surface plankton assemblage of species, at either or both stage, is interpreted within the context of the bathymetric distribution of species. The maxima in abundance and diversity occurred in February–March, for eggs, and May–June, for larvae. This 3-month time-lag between the stages is proposed to be related to the timing of egg spawning and larval recruitment to the pelagic environment. Mean egg abundances (82.4±29.8 eggs/10 m²) were 10-fold higher than the larval abundances (7.1±1.8 larvae/10 m²). Despite pronounced monthly variability, no statistically significant decrease in either egg or larvae abundance was observed during this 6-year study period. Compared with previous published studies, this study shows that the peak in ichthyoplankton diversity occurred two months earlier. In addition, the spawning period occurred over the whole year, even during autumn and winter. Using ordination techniques, the annual sequence appearance of taxa are described at the study site: Gadiforms, Ammodytidae and Pleuronectiforms were present during the winter whilst Sparidae, Blennidae, Labridae and Gobiidae, formed the summer group. Only three species, European anchovy Engraulis encrasicolus, European pilchard Sardina pilchardus and Atlantic horse mackerel Trachurus trachurus were recorded throughout the year.     

Textural and geochemical constraints on eruptive style of the 79 <Emphasis Type="SmallCaps">ad</Emphasis> eruption at Vesuvius

The 79 ad Plinian eruption of Vesuvius produced first a white pumice fallout from a high steady eruptive column, and then a grey pumice fallout originating from an oscillatory eruptive column with several partial column collapse events after which there was a total column collapse. This first total collapse was followed by renewed Plinian activity and produced the last grey pumice (GP) fallout deposit of the eruption. Textural characteristics (vesicularity and microcrystallinity) of a complete sequence of the pumice fallout deposits are presented along with the major element compositions and residual volatile contents (H₂O, Cl) to constrain the degassing processes and the eruptive dynamics. Large variations in residual volatile contents exist between the different eruptive units. Textural features also strongly differ between white and grey pumices, but also within the grey pumices. The degassing processes were thus highly heterogeneous. We propose a new model of the 79 ad eruption in which pre-eruptive conditions (H₂O saturation, magma temperature and viscosity) are the critical controls on the diversity of the syn-eruptive degassing processes and hence the eruptive dynamics. Cl contents measured in melt inclusions show that only the white pumice and the upper part of the grey pumice magma were H₂O saturated prior to eruption. The white pumice eruptive units represent a typical closed-system degassing evolution, whereas the first grey pumice one, stored under similar pre-eruptive saturation conditions, follows a particular open-system degassing evolution. We suggest that the oscillatory regime that dominated the grey pumice eruptive phase is linked to pre-eruptive water undersaturation of most of the grey magma, and the associated time delays necessary for H₂O exsolution. We also suggest that the high residual H₂O content of the last grey pumice, deposited after the renewal of Plinian activity following the first total column collapse event, is due to syn-eruptive saturation of GP magma and reduced H₂O exsolution efficiency resulting from speciation of dissolved H₂O in the melt.     

Active hydrothermal fluids circulation triggering small-scale collapse events: the case of the 2001–2002 fissure in the Lakki Plain (Nisyros Island,Aegean Sea,Greece)

Rip currents are fast moving, offshore flows that have the ability to move even the strongest swimmers into deeper waters. Miami Beach, Florida is one of the most visited beaches in the USA and a sought after destination for citizens and international tourists alike. It is also known to be a rip current “hot spot.” These factors greatly increase the risk of drowning; however, no previous research has focused on beachgoer perception of rip-related risks in South Florida. Over a 12-month period, 203 public surveys were collected to determine the rip current knowledge of beachgoers at Miami Beach based on factors such as swimming ability and frequency of beach visits. The responses were analyzed by constructing a normalized component factor to determine the respondent’s comprehensive knowledge of rips, and multiple regression models were used to assess the net influences of sociodemographic and behavioral characteristics on the responses. A significant proportion of the survey respondents showed insufficient knowledge, indicating they are at risk of drowning in a rip current. Frequent beachgoer’s exposure to the beach environment, maturation, and nativity is identified as the main contributors to knowledge net of other sociodemographic compositions. The most at-risk groups were determined to be young adults, foreign tourists, poor swimmers, and those who infrequently visited the beach. Miami Beach needs to initiate a rip current safety campaign to target these at-risk beachgoers, where interventions beyond familial and educational institutions should be introduced.     

Contrasting sedimentary processes along a convergent margin: the Lesser Antilles arc system

Sedimentation processes occurring in an active convergent setting are well illustrated in the Lesser Antilles island arc. The margin is related to westward subduction of the North and/or the South America plates beneath the Caribbean plate. From east to west, the arc can be subdivided into several tectono-sedimentary depositional domains: the accretionary prism, the fore-arc basin, the arc platform and inter-arc basin, and the Grenada back-arc basin. The Grenada back-arc basin, the fore-arc basin (Tobago Trough) and the accretionary prism on the east side of the volcanic arc constitute traps for particles derived from the arc platform and the South American continent. The arc is volcanically active, and provides large volumes of volcaniclastic sediments which accumulate mainly in the Grenada basin by volcaniclastic gravity flows (volcanic debris avalanches, debris flows, turbiditic flows) and minor amounts by fallout. By contrast, the eastern side of the margin is fed by ash fallout and minor volcaniclastic turbidites. In this area, the dominant component of the sediments is pelagic in origin, or derived from South America (siliciclastic turbidites). Insular shelves are the locations of carbonate sedimentation, such as large platforms which develop in the Limestone Caribbees in the northern part of the margin. Reworking of carbonate material by turbidity currents also delivers lesser amounts to eastern basins of the margin. This contrasting sedimentation on both sides of the arc platform along the margin is controlled by several interacting factors including basin morphology, volcanic productivity, wind and deep-sea current patterns, and sea-level changes. Basin morphology appears to be the most dominant factor. The western slopes of the arc platform are steeper than the eastern ones, thus favouring gravity flow processes.