718 research outputs found
Environmental DNA - An emerging tool in conservation for monitoring past and present biodiversity
AbstractThe continuous decline in Earth’s biodiversity represents a major crisis and challenge for the 21st century, and there is international political agreement to slow down or halt this decline. The challenge is in large part impeded by the lack of knowledge on the state and distribution of biodiversity – especially since the majority of species on Earth are un-described by science. All conservation efforts to save biodiversity essentially depend on the monitoring of species and populations to obtain reliable distribution patterns and population size estimates. Such monitoring has traditionally relied on physical identification of species by visual surveys and counting of individuals. However, traditional monitoring techniques remain problematic due to difficulties associated with correct identification of cryptic species or juvenile life stages, a continuous decline in taxonomic expertise, non-standardized sampling, and the invasive nature of some survey techniques. Hence, there is urgent need for alternative and efficient techniques for large-scale biodiversity monitoring. Environmental DNA (eDNA) – defined here as: genetic material obtained directly from environmental samples (soil, sediment, water, etc.) without any obvious signs of biological source material – is an efficient, non-invasive and easy-to-standardize sampling approach. Coupled with sensitive, cost-efficient and ever-advancing DNA sequencing technology, it may be an appropriate candidate for the challenge of biodiversity monitoring. Environmental DNA has been obtained from ancient as well as modern samples and encompasses single species detection to analyses of ecosystems. The research on eDNA initiated in microbiology, recognizing that culture-based methods grossly misrepresent the microbial diversity in nature. Subsequently, as a method to assess the diversity of macro-organismal communities, eDNA was first analyzed in sediments, revealing DNA from extinct and extant animals and plants, but has since been obtained from various terrestrial and aquatic environmental samples. Results from eDNA approaches have provided valuable insights to the study of ancient environments and proven useful for monitoring contemporary biodiversity in terrestrial and aquatic ecosystems. In the future, we expect the eDNA-based approaches to move from single-marker analyses of species or communities to meta-genomic surveys of entire ecosystems to predict spatial and temporal biodiversity patterns. Such advances have applications for a range of biological, geological and environmental sciences. Here we review the achievements gained through analyses of eDNA from macro-organisms in a conservation context, and discuss its potential advantages and limitations for biodiversity monitoring
Interactions of fines with base fractions of oil and its implication in smart water flooding
Abstract
Migration of fines, and formation of oil emulsion have been independently observed during smart water flooding both have been suggested to play a vital role in enhanced oil recovery (EOR). But, the exact role of fines and the reason of emulsion formation are not well studied for carbonate reservoirs. This study shows that addition of water and crude oil on calcite fines leads to formation of soluble oil emulsions in the water phase. Formation of these emulsions and its implication in EOR has been experimentally analyzed.
To characterize the formation of theses emulsions study has been conducted for various water insoluble salts were used as fines (including, Li2CO3, MgCO3, CaCO3, CaSO4, SrSO4, BaSO4 and reservoir CaCO3 fines). Different types of oil and water was added to these fines. To study conditions of oil emulsion formation, design oil was used consisting of hexane and hexadecane. Heptylamine and hexadecylamine were doped in various compositions to mimic the base number of the oil. Experiments were conducted for pure crude oil and doped oil to understand its implications in EOR. Composition of initial and final floating oil was obtained through gas chromatographic (GC) analysis. The two were thereafter compared to obtain the composition of micelles formed.
The experiments showed how oil emulsions were formed when polar hydrocarbons are present in the oil. Mixtures of alkanes did not produce emulsions. In oil containing hexadecylamine 95% of the initial hexadecylamine was accumulated in the emulsions and only 5% was found in the floating oil. In oil samples containing heptylamine only 45-50% of its initial amount was accumulated in the emulsions. This indicates heavier amines can form more stable emulsions. Oil emulsions were produced with all the fines used, but the composition of these emulsions were dependent on the salt anions. In all carbonates, lighter amines preferred emulsions formation with lighter alkane. No such selectivity was observed in any of the sulfates. Results obtained with crude, doped and designed oil were consistent for both pure salts and outcrops. These results show that fines of carbonate released during fracturing, or sulfates formed during smart water flooding can form mixed wet water soluble oil emulsions which help to mobilize trapped oil, and increase the sweep efficiency.
The results clearly show oils with the same base number can have significantly different amount of emulsion formation with fines, and provides a detailed mechanism of further characterization of the oil. The study highlights the significance of fines during smart water flooding in carbonate reservoirs and shows how its role in EOR can be mistakenly underestimated.</jats:p
Solubility Measurements and Modeling of Zinc, Lead and Iron Sulfides at High Temperatures and High Pressures
Observation of Motion Dependent Nonlinear Dispersion with Narrow Linewidth Atoms in an Optical Cavity
As an alternative to state-of-the-art laser frequency stabilisation using
ultra-stable cavities, it has been proposed to exploit the non-linear effects
from coupling of atoms with a narrow transition to an optical cavity. Here we
have constructed such a system and observed non-linear phase shifts of a narrow
optical line by strong coupling of a sample of strontium-88 atoms to an optical
cavity. The sample temperature of a few mK provides a domain where the Doppler
energy scale is several orders of magnitude larger than the narrow linewidth of
the optical transition. This makes the system sensitive to velocity dependent
multi-photon scattering events (Dopplerons) that affect the cavity field
transmission and phase. By varying the number of atoms and the intra-cavity
power we systematically study this non-linear phase signature which displays
roughly the same features as for much lower temperature samples. This
demonstration in a relatively simple system opens new possibilities for
alternative routes to laser stabilization at the sub 100 mHz level and
superradiant laser sources involving narrow line atoms. The understanding of
relevant motional effects obtained here has direct implications for other
atomic clocks when used in relation with ultranarrow clock transitions.Comment: 9 pages (including 4 pages of Supplemental Information), 6 figures.
Updated to correspond to the published versio
Non-linear Spectroscopy of Sr Atoms in an Optical Cavity for Laser Stabilization
We study the non-linear interaction of a cold sample of strontium-88 atoms
coupled to a single mode of a low finesse optical cavity in the so-called bad
cavity limit and investigate the implications for applications to laser
stabilization. The atoms are probed on the weak inter-combination line \lvert
5s^{2} \, ^1 \textrm{S}_0 \rangle \,-\, \lvert 5s5p \, ^3 \textrm{P}_1 \rangle
at 689 nm in a strongly saturated regime. Our measured observables include the
atomic induced phase shift and absorption of the light field transmitted
through the cavity represented by the complex cavity transmission coefficient.
We demonstrate high signal-to-noise-ratio measurements of both quadratures -
the cavity transmitted phase and absorption - by employing FM spectroscopy
(NICE-OHMS). We also show that when FM spectroscopy is employed in connection
with a cavity locked to the probe light, observables are substantially modified
compared to the free space situation where no cavity is present. Furthermore,
the non-linear dynamics of the phase dispersion slope is experimentally
investigated and the optimal conditions for laser stabilization are
established. Our experimental results are compared to state-of-the-art cavity
QED theoretical calculations.Comment: 7 pages, 4 figure
Multivariable Optimization of the Piperazine CO2 Post-Combustion Process
Abstract8 molal piperazine (PZ) is a promising solvent for developing an energy efficient CO2 post-combustion capture process. However, it has a limited operating range due to precipitation. The operating range can be extended by decreasing the piperazine concentration and/or increasing the CO2 loading of the lean solvent. However, optimal solvent composition must be determined taking into account the solvent circulation rate and the heat demand of the solvent regeneration.In this paper, we determine and generalize trends of performance for a broad range of operating conditions: 1.8 to 9mol PZ/ kg water, 0.2 to 0.6 lean loading, and for two flue gas sources: natural gas combined cycle power plant (NGCC, 3.9 mol% CO2) and a coal based power plant (ASC, 13.25 mol% CO2). Special attention is given to the boundaries where precipitation may occur. The results are created by the hybrid CAPCO2 rate-based model which accounts for precipitation when estimating the heat and mass transfer rates. The results show that the 7 molal piperazine gives the lowest specific reboiler duty at 0.40 CO2 lean loading: 3.32 GJ/t CO2 and 4.05 GJ/t CO2 for the ASC case and NGCC cases. The analysis also reveals that the capture process needs to be operated up to 7.8% above the minimum duty to avoid the risk of clogging due to solid formation. Note, this analysis assumes a 25°C minimum solvent temperature. The energy requirement of the capture process can be further improved by assuming a minimum solvent temperature of 30°C which gives a specific reboiler duty of 3.23 GJ/t CO2 (ASC case) and 3.80 GJ/t CO2 (NGCC case)
Kinetic study of a Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation
This paper focuses on carbon capture in an Ultra Super Critical power plant. The technology selected for CO2 capture is based on cooled ammonia scrubbing in post-combustion mode, as recently investigated by the authors in another work. Here, a rate-based approach is adopted. In detail, a specific primary energy consumption for CO2 avoided (SPECCA) of 2.77 MJ/kgCO2 is calculated in case of 85% of CO2 capture, with an ultimate power plant efficiency of 37.27%. Published by Elsevier Ltd
A Layout for the Carbon Capture with Aqueous Ammonia without Salt Precipitation
Post-combustion carbon capture technologies seem to be necessary to realize the CO2 mitigation policies internationally shared for the next future, despite none of them appears to be ready for full-scale applications. This work considers the aqueous ammonia-based process for a coal-fired Ultra Super Critical power plant. Two layouts are simulated with Aspen Plus employing the recently recalibrated Extended UNIQUAC thermodynamic model. The first one operates at chilling conditions, which yield to salt precipitation, and is taken as reference because already analyzed in previous studies. The second layout operates at cooled conditions, which does not yield any salt precipitation. The Chilled layout reveals low specific heat duty and SPECCA equal to 2.2 and 2.86 MJ/kgCO2, respectively. In contrast, the Cooled layout presents a higher specific heat duty of almost 3 MJ/kgCO2 but, importantly, a lower SPECCA of 2.58 MJ/kgCO2. The latter layout is a better choice also from the perspective of the plant operation since it does not present the salt precipitation
Experimental data of the aqueous NH3and CO2absorption at temperatures from 15 °C to 35 °C, NH3concentrations from 5% to 15% and CO2 loadings from 0.2 to 0.6 measured with the Wetted Wall Column
The absorption between aqueous NH3and CO2is studied using the Wetted Wall Column in order to show the effect of the solvent condition on the rate of reaction. A total of 27 different cases are investigated in the region defined by temperatures from 15 °C to 35 °C, NH3concentrations from 5% to 15% and CO2loadings from 0.2 to 0.6. The paper reports the data measured during the experiments, the experimental apparatus description and the experimental procedure. The data here presented are both the raw data measured with their uncertainty and the final value of the overall mass transfer coefficient. The overall mass transfer coefficient is the result of the raw data treatment explained in the research paper related to this data. The data here reported are analyzed in the paper by Lillia et al. (2018) [1]
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