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Few studies have evaluated the life cycle greenhouse gas (GHG) impacts associated with India's power sector, despite the expectation that it will dominate new thermal generation capacity additions over the coming decades. Here, we utilize India-specific supply chain data to estimate life cycle GHG emissions associated with power generated by combustion of Indian coal and liquefied natural gas (LNG) imported from the United States. Life cycle impacts of domestic coal power vary widely (80% confidence interval (CI): 951-1231 kg CO2eq/MWh) because of heterogeneity in existing power plant characteristics such as efficiency, age, and capacity. Less variability is observed for LNG sourced from northeast United States and used in the existing Indian combined cycle gas turbine (CCGT) fleet (80% CI: 523-648 kg CO2eq/MWh). On average, life cycle GHG emissions from LNG imported into India are â¼54% lower than those associated with Indian coal. However, the GHG intensity of the Indian coal-power sector may be reduced by 13% by retiring plants with the lowest efficiencies and replacing them with higher-efficiency supercritical plants. Improvement of the CCGT fleet efficiency from its current level (41%) to that of a new plant with an F-class turbine (50%) could reduce life cycle GHG emissions for LNG-sourced power by 19%.
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Carbón Mineral , Gases de Efecto Invernadero , Efecto Invernadero , India , New England , Centrales Eléctricas , Estados UnidosRESUMEN
We present a statistically enhanced version of the GreenHouse gas emissions of current Oil Sands Technologies model that facilitates characterization of variability of greenhouse gas (GHG) emissions associated with mining and upgrading of bitumen from Canadian oil sands. Over 30 years of publicly available project-specific operating data are employed as inputs, enabling Monte Carlo simulation of individual projects and the entire industry, for individual years and project life cycles. We estimate that median lifetime GHG intensities range from 89 to 137 kg CO2eq/bbl synthetic crude oil (SCO) for projects that employ upgrading. The only project producing dilbit that goes directly to a refinery has a median lifetime GHG intensity of 51 kg CO2eq/bbl dilbit. As SCO and dilbit are distinct products with different downstream processing energy requirements, a life cycle assessment ("well to wheel") is needed to properly compare them. Projects do not reach steady-state in terms of median GHG intensity. Projects with broader distributions of annual GHG intensities and higher median values are linked to specific events (e.g., project expansions). An implication for policymakers is that no specific technology or operating factor can be directly linked to GHG intensity and no particular project or year of operation can be seen as representative of the industry or production technology.
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Contaminantes Atmosféricos , Gases de Efecto Invernadero , Canadá , Efecto Invernadero , Yacimiento de Petróleo y Gas , Aceite de Brassica napusRESUMEN
Greenhouse gas (GHG) emissions associated with extraction of bitumen from oil sands can vary from project to project and over time. However, the nature and magnitude of this variability have yet to be incorporated into life cycle studies. We present a statistically enhanced life cycle based model (GHOST-SE) for assessing variability of GHG emissions associated with the extraction of bitumen using in situ techniques in Alberta, Canada. It employs publicly available, company-reported operating data, facilitating assessment of inter- and intraproject variability as well as the time evolution of GHG emissions from commercial in situ oil sands projects. We estimate the median GHG emissions associated with bitumen production via cyclic steam stimulation (CSS) to be 77 kg CO2eq/bbl bitumen (80% CI: 61-109 kg CO2eq/bbl), and via steam assisted gravity drainage (SAGD) to be 68 kg CO2eq/bbl bitumen (80% CI: 49-102 kg CO2eq/bbl). We also show that the median emissions intensity of Alberta's CSS and SAGD projects have been relatively stable from 2000 to 2013, despite greater than 6-fold growth in production. Variability between projects is the single largest source of variability (driven in part by reservoir characteristics) but intraproject variability (e.g., startups, interruptions), is also important and must be considered in order to inform research or policy priorities.
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Gases de Efecto Invernadero , Alberta , Efecto Invernadero , Yacimiento de Petróleo y Gas , VaporRESUMEN
In recent years, hydraulic fracturing and horizontal drilling have been applied to extract crude oil from tight reservoirs, including the Bakken formation. There is growing interest in understanding the greenhouse gas (GHG) emissions associated with the development of tight oil. We conducted a life cycle assessment of Bakken crude using data from operations throughout the supply chain, including drilling and completion, refining, and use of refined products. If associated gas is gathered throughout the Bakken well life cycle, then the well to wheel GHG emissions are estimated to be 89 g CO2eq/MJ (80% CI, 87-94) of Bakken-derived gasoline and 90 g CO2eq/MJ (80% CI, 88-94) of diesel. If associated gas is flared for the first 12 mo of production, then life cycle GHG emissions increase by 5% on average. Regardless of the level of flaring, the Bakken life cycle GHG emissions are comparable to those of other crudes refined in the United States because flaring GHG emissions are largely offset at the refinery due to the physical properties of this tight oil. We also assessed the life cycle freshwater consumptions of Bakken-derived gasoline and diesel to be 1.14 (80% CI, 0.67-2.15) and 1.22 barrel/barrel (80% CI, 0.71-2.29), respectively, 13% of which is associated with hydraulic fracturing.
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One of the major challenges in life cycle assessment (LCA) is the availability and quality of data used to develop models and to make appropriate recommendations. Approximations and assumptions are often made if appropriate data are not readily available. However, these proxies may introduce uncertainty into the results. A regression model framework may be employed to assess missing data in LCAs of products and processes. In this study, we develop such a regression-based framework to estimate CO2 emission factors associated with coal power plants in the absence of reported data. Our framework hypothesizes that emissions from coal power plants can be explained by plant-specific factors (predictors) that include steam pressure, total capacity, plant age, fuel type, and gross domestic product (GDP) per capita of the resident nations of those plants. Using reported emission data for 444 plants worldwide, plant level CO2 emission factors were fitted to the selected predictors by a multiple linear regression model and a local linear regression model. The validated models were then applied to 764 coal power plants worldwide, for which no reported data were available. Cumulatively, available reported data and our predictions together account for 74% of the total world's coal-fired power generation capacity.
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Contaminantes Atmosféricos/análisis , Dióxido de Carbono/análisis , Carbón Mineral , Electricidad , Centrales Eléctricas , Modelos Teóricos , IncertidumbreRESUMEN
We present results of a life cycle assessment (LCA) of Marcellus shale gas used for power generation. The analysis employs the most extensive data set of any LCA of shale gas to date, encompassing data from actual gas production and power generation operations. Results indicate that a typical Marcellus gas life cycle yields 466 kg CO2eq/MWh (80% confidence interval: 450-567 kg CO2eq/MWh) of greenhouse gas (GHG) emissions and 224 gal/MWh (80% CI: 185-305 gal/MWh) of freshwater consumption. Operations associated with hydraulic fracturing constitute only 1.2% of the life cycle GHG emissions, and 6.2% of the life cycle freshwater consumption. These results are influenced most strongly by the estimated ultimate recovery (EUR) of the well and the power plant efficiency: increase in either quantity will reduce both life cycle freshwater consumption and GHG emissions relative to power generated at the plant. We conclude by comparing the life cycle impacts of Marcellus gas and U.S. coal: The carbon footprint of Marcellus gas is 53% (80% CI: 44-61%) lower than coal, and its freshwater consumption is about 50% of coal. We conclude that substantial GHG reductions and freshwater savings may result from the replacement of coal-fired power generation with gas-fired power generation.
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Agua Dulce , Gases , Efecto InvernaderoRESUMEN
Adhesion flow assays are commonly employed to characterize the kinetics and force-dependence of receptor-ligand interactions. As transient cellular adhesion events are often mediated by a small number of receptor-ligand complexes (tether bonds) their durations are highly variable, which in turn presents obstacles to standard methods of analysis. In this paper, we employ the stochastic approach to chemical kinetics to construct the pause time distribution. Using this distribution, we develop a robust maximum likelihood (ML) approach to the robust estimation of rate constants associated with receptor-mediated transient adhesion and their confidence intervals. We then formulate robust estimators of the parameters of models for the force-dependence of the off-rate. Lastly, we develop a robust method of elucidation of the force-dependence of the off-rate using Akaike's information criterion (AIC). Our findings conclusively demonstrate that ML estimators of adhesion kinetics are substantial improvements over more conventional approaches, and when combined with Fisher information, they may be used to objectively and reproducibly distinguish the kinetics of different receptor-ligand complexes. Software for the implementation of these methods with experimental data is publicly available as for download at http://www.laurenzi.net.
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Receptores de Superficie Celular/metabolismo , Animales , Adhesión Celular , Cinética , Funciones de Verosimilitud , Modelos Biológicos , Método de Montecarlo , Análisis de Regresión , Procesos Estocásticos , Factores de TiempoRESUMEN
BACKGROUND: Although oligonucleotide microarray technology is ubiquitous in genomic research, reproducibility and standardization of expression measurements still concern many researchers. Cross-hybridization between microarray probes and non-target ssDNA has been implicated as a primary factor in sensitivity and selectivity loss. Since hybridization is a chemical process, it may be modeled at a population-level using a combination of material balance equations and thermodynamics. However, the hybridization reaction network may be exceptionally large for commercial arrays, which often possess at least one reporter per transcript. Quantification of the kinetics and equilibrium of exceptionally large chemical systems of this type is numerically infeasible with customary approaches. RESULTS: In this paper, we present a robust and computationally efficient algorithm for the simulation of hybridization processes underlying microarray assays. Our method may be utilized to identify the extent to which nucleic acid targets (e.g. cDNA) will cross-hybridize with probes, and by extension, characterize probe robustnessusing the information specified by MAGE-TAB. Using this algorithm, we characterize cross-hybridization in a modified commercial microarray assay. CONCLUSIONS: By integrating stochastic simulation with thermodynamic prediction tools for DNA hybridization, one may robustly and rapidly characterize of the selectivity of a proposed microarray design at the probe and "system" levels. Our code is available at http://www.laurenzi.net.
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Algoritmos , Biología Computacional/métodos , ADN/química , Análisis de Secuencia por Matrices de Oligonucleótidos/métodos , Perfilación de la Expresión Génica , Hibridación de Ácido NucleicoRESUMEN
Autocatalysis is a ubiquitous chemical process that drives a plethora of biological phenomena, including the self-propagation of prions etiological to the Creutzfeldt-Jakob disease and bovine spongiform encephalopathy. To explain the dynamics of these systems, we have solved the chemical master equation for the irreversible autocatalytic reaction A+B-->2A. This solution comprises the first closed form expression describing the probabilistic time evolution of the populations of autocatalytic and noncatalytic molecules from an arbitrary initial state. Grand probability distributions are likewise presented for autocatalysis in the equilibrium limit (A+B <==>2A), allowing for the first mechanistic comparison of this process with chemical isomerization (B<==>A) in small systems. Although the average population of autocatalytic (i.e., prion) molecules largely conforms to the predictions of the classical "rate law" approach in time and the law of mass action at equilibrium, thermodynamic differences between the entropies of isomerization and autocatalysis are revealed, suggesting a "mechanism dependence" of state variables for chemical reaction processes. These results demonstrate the importance of chemical mechanism and molecularity in the development of stochastic processes for chemical systems and the relationship between the stochastic approach to chemical kinetics and nonequilibrium thermodynamics.
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Botrocetin is a snake venom protein that enhances the affinity of the A1 domain of plasma von Willebrand factor (vWF) for the platelet receptor glycoprotein Ibalpha (GPIbalpha), an event that contributes to bleeding and host death. Here we describe a kinetic and crystallographic analysis of this interaction that reveals a novel mechanism of affinity enhancement. Using high-temporal-resolution microscopy, we show that botrocetin decreases the GPIbalpha off-rate two-fold in both human and mouse complexes without affecting the on-rate. The key to this behavior is that, upon binding of GPIbalpha to vWF-A1, botrocetin prebound to vWF-A1 makes no contacts initially with GPIbalpha, but subsequently slides around the A1 surface to form a new interface. This two-step mechanism and flexible coupling may prevent adverse alterations in on-rate of GPIbalpha for vWF-A1, and permit adaptation to structural differences in GPIbalpha and vWF in several prey species.
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Venenos de Crotálidos/farmacología , Agregación Plaquetaria/efectos de los fármacos , Secuencia de Aminoácidos , Animales , Sitios de Unión , Plaquetas/química , Plaquetas/efectos de los fármacos , Plaquetas/metabolismo , Venenos de Crotálidos/química , Cristalografía por Rayos X , Humanos , Cinética , Ratones , Modelos Moleculares , Datos de Secuencia Molecular , Adhesividad Plaquetaria , Complejo GPIb-IX de Glicoproteína Plaquetaria/química , Complejo GPIb-IX de Glicoproteína Plaquetaria/metabolismo , Unión Proteica , Estructura Terciaria de Proteína , Alineación de Secuencia , Factor de von Willebrand/química , Factor de von Willebrand/metabolismoRESUMEN
Many anatomical differences exist between males and females; these are manifested on a molecular level by different hormonal environments. Although several molecular differences in adult tissues have been identified, a comprehensive investigation of the gene expression differences between males and females has not been performed. We surveyed the expression patterns of 13,977 mouse genes in male and female hypothalamus, kidney, liver, and reproductive tissues. Extensive differential gene expression was observed not only in the reproductive tissues, but also in the kidney and liver. The differentially expressed genes are involved in drug and steroid metabolism, osmotic regulation, or as yet unresolved cellular roles. In contrast, very few molecular differences were observed between the male and female hypothalamus in both mice and humans. We conclude that there are persistent differences in gene expression between adult males and females. These molecular differences have important implications for the physiological differences between males and females.
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Regulación de la Expresión Génica/genética , Genitales/metabolismo , Riñón/metabolismo , Hígado/metabolismo , Preparaciones Farmacéuticas/metabolismo , Caracteres Sexuales , Animales , ADN/análisis , ADN/genética , Femenino , Perfilación de la Expresión Génica , Genitales/citología , Humanos , Hipotálamo/citología , Hipotálamo/metabolismo , Riñón/citología , Hígado/citología , Masculino , Tasa de Depuración Metabólica/genética , Ratones , Análisis de Secuencia por Matrices de Oligonucleótidos , Especificidad de Órganos , Ovario/citología , Ovario/metabolismo , Receptores de Superficie Celular/genética , Serpinas , Testículo/citología , Testículo/metabolismo , TranscortinaRESUMEN
Platelet-type von Willebrand disease (PTVWD) is a bleeding disorder in which an increase of function mutation in glycoprotein Ibalpha (GPIbalpha), with respect to binding of von Willebrand factor (VWF), results in a loss of circulating high molecular weight VWF multimers together with a mild-moderate thrombocytopenia. To better ascertain the specific perturbations in adhesion associated with this disease state, we performed a detailed analysis of the kinetic and mechanical properties of tether bonds formed between PT-VWD platelets and the A1-domain of VWF. Results indicate that the GPIbalpha mutation, Gly233Val, promotes and stabilizes platelet adhesion to VWF at shear rates that do not support binding between the native receptor-ligand pair due to enhanced formation and increased longevity of the mutant tether bond (k0 off values for mutant versus native complex of 0.67 +/- 0.11 s-1 and 3.45 +/- 0.37 s-1, respectively). By contrast, the sensitivity of this interaction to an applied force, a measure of bond strength, was similar to the wild-type (WT) receptor. Although the observed alterations in the intrinsic properties of the GPIbalpha-VWF tether bond are comparable to those reported for the type 2B VWD, distinct molecular mechanisms may be responsible for these function-enhancing bleeding disorders, as interactions between the mutant receptor and mutant ligand resulted in a greater stability in platelet adhesion. We speculate that the enhanced cellular on-rate together with the prolongation in the lifetime of the mutant receptor-ligand bond contributes to platelet aggregation in circulating blood by permitting the formation of multiple GPIbalpha-VWF-A1 interactions.
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Mutación Missense , Complejo GPIb-IX de Glicoproteína Plaquetaria/genética , Complejo GPIb-IX de Glicoproteína Plaquetaria/metabolismo , Enfermedades de von Willebrand/genética , Factor de von Willebrand/metabolismo , Plaquetas/química , Plaquetas/metabolismo , Heterocigoto , Humanos , Cinética , Modelos Químicos , Perfusión , Adhesividad Plaquetaria/genética , Unión Proteica/genética , Estrés MecánicoRESUMEN
The ability of platelets to tether to and translocate on injured vascular endothelium relies on the interaction between the platelet glycoprotein receptor Ib alpha (GPIb(alpha)) and the A1 domain of von Willebrand factor (vWF-A1). To date, limited information exists on the kinetics that govern platelet interactions with vWF in hemodynamic flow. We now report that the GPIb(alpha)-vWF-A1 tether bond displays similar kinetic attributes as the selectins including: 1) the requirement for a critical level of hydrodynamic flow to initiate adhesion, 2) short-lived tethering events at sites of vascular injury in vivo, and 3) a fast intrinsic dissociation rate constant, k(0)(off) (3.45 +/- 0.37 s(-1)). Values for k(off), as determined by pause time analysis of transient capture/release events, were also found to vary exponentially (4.2 +/- 0.8 s(-1) to 7.3 +/- 0.4 s(-1)) as a function of the force applied to the bond (from 36 to 217 pN). The biological importance of rapid bond dissociation in platelet adhesion is demonstrated by kinetic characterization of the A1 domain mutation, I546V that is associated with type 2B von Willebrand disease (vWD), a bleeding disorder that is due to the spontaneous binding of plasma vWF to circulating platelets. This mutation resulted in a loss of the shear threshold phenomenon, a approximately sixfold reduction in k(off), but no significant alteration in the ability of the tether bond to resist shear-induced forces. Thus, flow dependent adhesion and rapid and force-dependent kinetic properties are the predominant features of the GPIb(alpha)-vWF-A1 tether bond that in part may explain the preferential binding of platelets to vWF at sites of vascular injury, the lack of spontaneous platelet aggregation in circulating blood, and a mechanism to limit thrombus formation.