Search Results Heading

MBRLSearchResults

mbrl.module.common.modules.added.book.to.shelf
Title added to your shelf!
View what I already have on My Shelf.
Oops! Something went wrong.
Oops! Something went wrong.
While trying to add the title to your shelf something went wrong :( Kindly try again later!
Are you sure you want to remove the book from the shelf?
Oops! Something went wrong.
Oops! Something went wrong.
While trying to remove the title from your shelf something went wrong :( Kindly try again later!
    Done
    Filters
    Reset
  • Discipline
      Discipline
      Clear All
      Discipline
  • Is Peer Reviewed
      Is Peer Reviewed
      Clear All
      Is Peer Reviewed
  • Item Type
      Item Type
      Clear All
      Item Type
  • Subject
      Subject
      Clear All
      Subject
  • Year
      Year
      Clear All
      From:
      -
      To:
  • More Filters
      More Filters
      Clear All
      More Filters
      Source
    • Language
891 result(s) for "Evaporites"
Sort by:
Dry/Wet Cycling and the Thermodynamics and Kinetics of Prebiotic Polymer Synthesis
The endoergic nature of protein and nucleic acid assembly in aqueous media presents two questions that are fundamental to the understanding of life’s origins: (i) how did the polymers arise in an aqueous prebiotic world; and (ii) once formed in some manner, how were they sufficiently persistent to engage in further chemistry. We propose here a quantitative resolution of these issues that evolved from recent accounts in which RNA-like polymers were produced in evaporation/rehydration cycles. The equilibrium Nm + Nn ↔ Nm+n + H2O is endoergic by about 3.3 kcal/mol for polynucleotide formation, and the system thus lies far to the left in the starting solutions. Kinetic simulations of the evaporation showed that simple Le Châtelier’s principle shifts were insufficient, but the introduction of oligomer-stabilizing factors of 5–10 kcal/mol both moved the process to the right and respectively boosted and retarded the elongation and hydrolysis rates. Molecular crowding and excluded volume effects in present-day cells yield stabilizing factors of that order, and we argue here that the crowded conditions in the evaporites generate similar effects. Oligomer formation is thus energetically preferred in those settings, but the process is thwarted in each evaporation step as diffusion becomes rate limiting. Rehydration dissipates disordered oligomer clusters in the evaporites, however, and subsequent dry/wet cycling accordingly “ratchets up” the system to an ultimate population of kinetically trappedthermodynamically preferred biopolymers.
Global distribution of carbonate rocks and karst water resources
Karst regions offer a variety of natural resources such as freshwater and biodiversity, and many cultural resources. The World Karst Aquifer Map (WOKAM) is the first detailed and complete global geodatabase concerning the distribution of karstifiable rocks (carbonates and evaporites) representing potential karst aquifers. This study presents a statistical evaluation of WOKAM, focusing entirely on karst in carbonate rocks and addressing four main aspects: (1) global occurrence and geographic distribution of karst; (2) karst in various topographic settings and coastal areas; (3) karst in different climatic zones; and (4) populations living on karst. According to the analysis, 15.2% of the global ice-free continental surface is characterized by the presence of karstifiable carbonate rock. The largest percentage is in Europe (21.8%); the largest absolute area occurs in Asia (8.35 million km2). Globally, 31.1% of all surface exposures of carbonate rocks occur in plains, 28.1% in hills and 40.8% in mountains, and 151,400 km or 15.7% of marine coastlines are characterized by carbonate rocks. About 34.2% of all carbonate rocks occur in arid climates, followed by 28.2% in cold and 15.9% in temperate climates, whereas only 13.1 and 8.6% occur in tropical and polar climates, respectively. Globally, 1.18 billion people (16.5% of the global population) live on karst. The highest absolute number occurs in Asia (661.7 million), whereas the highest percentages are in Europe (25.3%) and North America (23.5%). These results demonstrate the global importance of karst and serve as a basis for further research and international water management strategies.
Animal evolution, bioturbation, and the sulfate concentration of the oceans
As recognized already by Charles Darwin, animals are geobiological agents. Darwin observed that worms aerate and mix soils on a massive scale, aiding in the decomposition of soil organic matter. A similar statement can be made about marine benthic animals. This mixing, also known as bioturbation, not only aides in the decomposition of sedimentary organic material, but as contended here, it has also significantly influenced the chemistry of seawater. In particular, it is proposed that sediment mixing by bioturbating organisms resulted in a severalfold increase in seawater sulfate concentration. For this reason, the evolution of bioturbation is linked to the significant deposition of sulfate evaporate minerals, which is largely a phenomena of the Phanerozoic, the last 542 million years and the time over which animals rose to prominence.
Unique Neoproterozoic carbon isotope excursions sustained by coupled evaporite dissolution and pyrite burial
The Neoproterozoic era witnessed a succession of biological innovations that culminated in diverse animal body plans and behaviours during the Ediacaran–Cambrian radiations. Intriguingly, this interval is also marked by perturbations to the global carbon cycle, as evidenced by extreme fluctuations in climate and carbon isotopes. The Neoproterozoic isotope record has defied parsimonious explanation because sustained 12C-enrichment (low δ13C) in seawater seems to imply that substantially more oxygen was consumed by organic carbon oxidation than could possibly have been available. We propose a solution to this problem, in which carbon and oxygen cycles can maintain dynamic equilibrium during negative δ13C excursions when surplus oxidant is generated through bacterial reduction of sulfate that originates from evaporite weathering. Coupling of evaporite dissolution with pyrite burial drives a positive feedback loop whereby net oxidation of marine organic carbon can sustain greenhouse forcing of chemical weathering, nutrient input and ocean margin euxinia. Our proposed framework is particularly applicable to the late Ediacaran ‘Shuram’ isotope excursion that directly preceded the emergence of energetic metazoan metabolisms during the Ediacaran–Cambrian transition. Here we show that non-steady-state sulfate dynamics contributed to climate change, episodic ocean oxygenation and opportunistic radiations of aerobic life during the Neoproterozoic era.
The World Karst Aquifer Mapping project: concept, mapping procedure and map of Europe
Karst aquifers contribute substantially to freshwater supplies in many regions of the world, but are vulnerable to contamination and difficult to manage because of their unique hydrogeological characteristics. Many karst systems are hydraulically connected over wide areas and require transboundary exploration, protection and management. In order to obtain a better global overview of karst aquifers, to create a basis for sustainable international water-resources management, and to increase the awareness in the public and among decision makers, the World Karst Aquifer Mapping (WOKAM) project was established. The goal is to create a world map and database of karst aquifers, as a further development of earlier maps. This paper presents the basic concepts and the detailed mapping procedure, using France as an example to illustrate the step-by-step workflow, which includes generalization, differentiation of continuous and discontinuous carbonate and evaporite rock areas, and the identification of non-exposed karst aquifers. The map also shows selected caves and karst springs, which are collected in an associated global database. The draft karst aquifer map of Europe shows that 21.6% of the European land surface is characterized by the presence of (continuous or discontinuous) carbonate rocks; about 13.8% of the land surface is carbonate rock outcrop.
Unraveling the Origin of the Messinian? Evaporites in Zakynthos Island, Ionian Sea: Implications for the Sealing Capacity in the Mediterranean Sea
The new approach on depositional conditions of the Messinian evaporites in Zakynthos Island indicates that the evaporites in the Kalamaki and Ag. Sostis areas were redeposited during the Early Pliocene. They accumulated either as turbiditic evaporites or as slumped blocks, as a response to Kalamaki thrust activity. Thrust activity developed a narrow and restricted Kalamaki foreland basin with the uplifted orogenic wedge consisting of Messinian evaporites. These evaporites eroded and redeposited in the foreland basin as submarine fans with turbiditic currents or slumped blocks (olistholiths) that consist of Messinian evaporites. These conditions occurred just before the inundation of the Mediterranean, during or prior to the Early Pliocene (Zanclean). Following the re-sedimentation of the Messinian evaporites, the inundation of the Mediterranean produced the “Lago Mare” fine-grained sediments that rest unconformably over the resedimented evaporites. The “Trubi” limestones were deposited later. It is critical to understand the origin of the “Messinian” Evaporites because they can serve as an effective seal rock for the oil and gas industry. It is thus important to evaluate their thickness and distribution into the SE Mediterranean Sea.
A >200 ka U‐Th Based Chronology From Lacustrine Evaporites, Searles Lake, CA
Well‐dated lacustrine records are essential to establish the timing and drivers of regional hydroclimate change. Searles Basin, California, records the depositional history of a fluctuating saline‐alkaline lake in the terminal basin of the Owens River system draining the eastern Sierra Nevada. Here, we establish a U‐Th chronology for the ∼76‐m‐long SLAPP‐SLRS17 core collected in 2017 based on dating of evaporite minerals. Ninety‐eight dated samples comprising nine different minerals were evaluated based on stratigraphic, mineralogic, textural, chemical, and reproducibility criteria. After the application of these criteria, a total of 37 dated samples remained as constraints for the age model. A lack of dateable minerals between 145 and 110 ka left the age model unconstrained over the penultimate glacial termination (Termination II). We thus established a tie point between plant wax δD values in the core and a nearby speleothem δ18O record at the beginning of the Last Interglacial. We construct a Bayesian age model allowing stratigraphy to inform sedimentation rate inflections. We find that the >210 ka SLAPP‐SRLS17 record contains five major units that correspond with prior work. The new dating is broadly consistent with previous efforts but provides more precise age estimates and enables a detailed evaluation of evaporite depositional history. We also offer a substantial revision of the age of the Bottom Mud‐Mixed Layer contact, shifting it from ∼130 ka to 178 ± 3 ka. The new U‐Th chronology documents the timing of mud and salt layers and lays the foundation for climate reconstructions. Plain Language Summary Searles Lake, California, is currently a dry saltpan; however, in the past, it was a large and deep lake (>200 m). Lake levels have varied with changes in climate. These changes influenced the sediments deposited. Thus, changes in the lake sediments can be applied to understand the past environments of the region. Here, we developed a chronology for a 76‐m‐long sediment core using isotopic dating methods. The lake sediments contain many different minerals which can be dated. However, some of these minerals formed after the lake sediments were deposited and others have been chemically altered in the time since their formation. We developed criteria for the selection of samples that are the most likely to reflect the age of sediment deposition. We used the selected ages along with statistical modeling to determine the ages of the sediments with depth. We find that the core contains a record that spans over 200,000 years, including the last two glacial cycles. The age model presented here lays the foundation for the exploration of how past climate changes impacted water availability and vegetation in southeastern California. Key Points >200 ka‐long sediment record of southwestern North American paleoenvironment Establishes general criteria for selection of evaporite minerals for U‐Th dating Explores a wide range of parameters for Bayesian age‐depth modeling
A fundamental role of carbonate–sulfate melts in the formation of iron oxide–apatite deposits
Genetic models for iron oxide–apatite deposits are controversial and span a spectrum from orthomagmatic to hydrothermal endmembers. This lack of consensus is rooted in uncertainties as to the nature and origin of ore-forming fluids in these systems. Here, we present a fluid-inclusion study of mineralizing fluids at two iron oxide–apatite deposits (Buena Vista, Nevada and Iron Springs, Utah). We found that the inclusions in both systems comprise both aqueous brine and ubiquitous iron-rich carbonate–sulfate melts. These melts were found throughout the paragenesis of both deposits and show a tremendous capacity to transport ferric iron. Hence, we argue that orthomagmatic fluids played a role in mineralization at both Buena Vista and Iron Springs, and that the main ore-forming fluid was an iron-rich carbonate–sulfate melt formed by the assimilation and anatexis of evaporite-bearing carbonate rocks. The geological conditions that give rise to carbonate–sulfate melts are also a common feature of other classic iron oxide–apatite systems worldwide. Hence, we argue that the process of assimilation, anatexis and immiscibility of carbonate–sulfate melts is fundamental to iron oxide–apatite formation and provides a common link between iron oxide–apatite systems in different geological settings.Iron-rich carbonate–sulfate melts are fundamental to the formation of iron oxide–apatite ore deposits, according to a detailed fluid-inclusion study that characterized the mineralizing fluids for two mineralizing systems in the United States.
Landslides in the Remolinos gypsum escarpment (NE Spain): controls imposed by stratigraphy, fluvial erosion, and interstratal salt dissolution
Dissolution of karst rocks (evaporites and carbonates) can cause significant mechanical weakening, but its preparatory role for landslide development has been scarcely explored. Fluvial valleys carved in gypsum bedrock typically display prominent escarpments with numerous landslides and perched valleys indicative of rapid retreat rate. The stratigraphic and cartographic analysis of the 37-km-long Remolinos gypsum escarpment in the Ebro Valley (NE Spain) reveals that landslide types are controlled by the lithological succession: (1) rotational slides in sections with mudstones and marls at the base; (2) rock-slope collapses (massive rock-falls) where the cliff includes halite packages at the foot; and (3) relatively small rock-falls and topples being the main failures affecting cliffs entirely made by gypsum. Fluvial undercutting by the highly mobile Ebro River is the main process that controls the spatial and temporal distribution of slope instability. Geomorphic and chronological evidence supports that the abandonment in 1574 of the El Castellar village was at least partially motivated by a shift in the river channel toward the escarpment and the consequent landslide activity. Several lines of evidence support the concept whereby interstratal salt dissolution (halite and glauberite), here designated as subsurface solutional undermining, play a significant preparatory role for landslide development: (1) dissolution of salt close to the scarp by the inward advance of dissolution fronts and subsidence of the overlying strata; (2) collapsed fault blocks with no offset across the grabens; and (3) brine seepages and extensive efflorescences and precipitates of Na-sulfates and halite.