125 research outputs found
Game Theoretic Analysis of Carbon Emission Reduction and Sales Promotion in Dyadic Supply Chain in Presence of Consumers’ Low-Carbon Awareness
The paper studies how the combination of the manufacturer’s carbon emission reduction and the retailer’s emission reduction relevant promotion impacts the performances of a dyadic supply chain in low-carbon environment. We consider three typical scenarios, that is, centralized and decentralized without or with side-payment. We compare measures of supply chain performances, such as profitabilities, emission reduction efficiencies, and effectiveness, in these scenarios. To improve chain-wide performances, a new side-payment contract is designed to coordinate the supply chain and numerical experiments are also conducted. We find the following. (1) In decentralized setting, the retailer will provide emission cutting allowance to the manufacturer only if their unit product profit margin is higher enough than the manufacturer’s, and the emission reduction level of per unit product is a monotonically increasing function with respect to the cost pooling proportion provided by the retailer; (2) the new side-payment contract can coordinate the dyadic supply chain successfully due to its integrating sales promotion effort and emission reduction input, which results in system pareto optimality under decentralized individual rationality but achieves a collective rationality effect in the centralized setting; (3) when without external force’s regulation, consumers’ low-carbon awareness is to enhance consumers’ utility and decrease profits of supply chain firms
TUFM in health and disease: exploring its multifaceted roles
The nuclear-encoded mitochondrial protein Tu translation elongation factor, mitochondrial (TUFM) is well-known for its role in mitochondrial protein translation. Originally discovered in yeast, TUFM demonstrates significant evolutionary conservation from prokaryotes to eukaryotes. Dysregulation of TUFM has been associated with mitochondrial disorders. Although early hypothesis suggests that TUFM is localized within mitochondria, recent studies identify its presence in the cytoplasm, with this subcellular distribution being linked to distinct functions of TUFM. Significantly, in addition to its established function in mitochondrial protein quality control, recent research indicates a broader involvement of TUFM in the regulation of programmed cell death processes (e.g., autophagy, apoptosis, necroptosis, and pyroptosis) and its diverse roles in viral infection, cancer, and other disease conditions. This review seeks to offer a current summary of TUFM’s biological functions and its complex regulatory mechanisms in human health and disease. Insight into these intricate pathways controlled by TUFM may lead to the potential development of targeted therapies for a range of human diseases
Soil conservation and water conservation services and trade-offs following the land consolidation project: a case study of Yan’an city, China
The Loess Plateau is an important region for soil and water conservation and ecological construction in China. Exploring the spatio-temporal variations in soil conservation and water conservation services and their relationships in Loess Plateau under the background of land consolidation projects is of great significance for ecological protection and quality development in the Yellow River Basin. Taking Yan’an city as the research area, this paper used the InVEST model to quantitatively evaluated spatio-temporal variation characteristics and trade-off/synergy relationship of the soil conservation and water conservation services from 2010 to 2018. According to the implementation data, the relationship between the gully control and land consolidation (GCLC) project in various counties of Yan’an city and soil conservation and water conservation service was analyzed. The results showed that the total amount of soil conservation services in Yan’an City were 4.07 × 106 t and 3.75 × 106 t in 2010 and 2018 with a decrease of 7.76%, and with low spatial clustering characteristic. The total amount of water conservation services were 2.01 × 1010 mm and 2.03 × 1010 mm in 2010 and 2018 with a increase of 0.56%, and with high spatial clustering characteristic. There is a synergistic relationship between soil conservation and water conservation services in most area of Yan’an city. From 2010 to 2018, the effect of the GCLC projects on soil conservation and water conservation services in Yan’an city is not significant. The GCLC project can effectively alleviate the situation of sharp decline of cultivated land area and insufficient food production capacity
The East-Asian VLBI Network
The East-Asian VLBI Network (EAVN) is the international VLBI facility in East
Asia and is conducted in collaboration with China, Japan, and Korea. The EAVN
consists of VLBI arrays operated in each East Asian country, containing 21
radio telescopes and three correlators. The EAVN will be mainly operated at 6.7
(C-band), 8 (X-band), 22 (K-band), and 43 GHz (Q-band), although the EAVN has
an ability to conduct observations at 1.6 - 129 GHz. We have conducted fringe
test observations eight times to date at 8 and 22 GHz and fringes have been
successfully detected at both frequencies. We have also conducted science
commissioning observations of 6.7 GHz methanol masers in massive star-forming
regions. The EAVN will be operational from the second half of 2017, providing
complementary results with the FAST on AGNs, massive star-forming regions, and
evolved stars with high angular resolution at cm- to mm-wavelengths.Comment: 6 pages, 3 figures, 2 tables. To appear in the proceedings of
"Frontiers in Radio Astronomy and FAST Early Sciences Symposium 2015" ed. Lei
Qian (ASP Conf. Ser.
Fast, multicolor photodetection with graphene-contacted p-GaSe/n-InSe van der Waals heterostructures
The integration of different two-dimensional materials within a multilayer van der Waals (vdW) heterostructure offers a promising technology for high performance opto-electronic devices such as photodetectors and light sources. Here we report on the fabrication and electronic properties of vdW heterojunction diodes composed of the direct band gap layered semiconductors InSe and GaSe and transparent monolayer graphene electrodes. We show that the type II band alignment between the two layered materials and their distinctive spectral response, combined with the short channel length and low electrical resistance of graphene electrodes, enable efficient generation and extraction of photoexcited carriers from the heterostructure even when no external voltage is applied. Our devices are fast ( ~ 1 ÎĽs), self-driven photodetectors with multicolor photoresponse ranging from the ultraviolet to the near-infrared and offer new routes to miniaturized optoelectronics beyond present semiconductor materials and technologies
Study on closing and cracking stress calculation method of fractured rock
Determining the characteristic stress intensity according to the rock stress-strain curve is significant significance for rock engineering. Nowadays, there are relatively mature methods for determining peak stress and damage stress. However, the crack volume strain method, axial strain method, and strain response method are more subjective to determine rock’s closure stress and initiation stress. The closure rock stress and crack initiation stress refined value method are proposed based on these methods, which are based on the discreteness of the rock stress and strain point. Through optimizing the stress characteristics by an objective function (variance function), the subjectivity of artificial observation is avoided; Based on the trend of rock stress-strain curve, an empirical method for determining rock closure stress and crack initiation stress is proposed. The test results indicate that the two proposed methods that calculate closure rock stress and crack initiation stress can obtain reasonable results. These methods can be used as a supplement to the characteristics of the rock stress determination method and can be used in actual engineering
N2O isotopocule measurements using laser spectroscopy:analyzer characterization and intercomparison
For the past two decades, the measurement of nitrous oxide (N2O) isotopocules – isotopically substituted molecules 14N15N16O, 15N14N16O and 14N14N18O of the main isotopic species 14N14N16O – has been a promising technique for understanding N2O production and consumption pathways. The coupling of non-cryogenic and tuneable light sources with different detection schemes, such as direct absorption quantum cascade laser absorption spectroscopy (QCLAS), cavity ring-down spectroscopy (CRDS) and off-axis integrated cavity output spectroscopy (OA-ICOS), has enabled the production of commercially available and field-deployable N2O isotopic analyzers. In contrast to traditional isotope-ratio mass spectrometry (IRMS), these instruments are inherently selective for position-specific 15N substitution and provide real-time data, with minimal or no sample pretreatment, which is highly attractive for process studies.
Here, we compared the performance of N2O isotope laser spectrometers with the three most common detection schemes: OA-ICOS (N2OIA-30e-EP, ABB – Los Gatos Research Inc.), CRDS (G5131-i, Picarro Inc.) and QCLAS (dual QCLAS and preconcentration, trace gas extractor (TREX)-mini QCLAS, Aerodyne Research Inc.). For each instrument, the precision, drift and repeatability of N2O mole fraction [N2O] and isotope data were tested. The analyzers were then characterized for their dependence on [N2O], gas matrix composition (O2, Ar) and spectral interferences caused by H2O, CO2, CH4 and CO to develop analyzer-specific correction functions. Subsequently, a simulated two-end-member mixing experiment was used to compare the accuracy and repeatability of corrected and calibrated isotope measurements that could be acquired using the different laser spectrometers.
Our results show that N2O isotope laser spectrometer performance is governed by an interplay between instrumental precision, drift, matrix effects and spectral interferences. To retrieve compatible and accurate results, it is necessary to include appropriate reference materials following the identical treatment (IT) principle during every measurement. Remaining differences between sample and reference gas compositions have to be corrected by applying analyzer-specific correction algorithms. These matrix and trace gas correction equations vary considerably according to N2O mole fraction, complicating the procedure further. Thus, researchers should strive to minimize differences in composition between sample and reference gases. In closing, we provide a calibration workflow to guide researchers in the operation of N2O isotope laser spectrometers in order to acquire accurate N2O isotope analyses. We anticipate that this workflow will assist in applications where matrix and trace gas compositions vary considerably (e.g., laboratory incubations, N2O liberated from wastewater or groundwater), as well as extend to future analyzer models and instruments focusing on isotopic species of other molecules.ISSN:1867-1381ISSN:1867-854
NO isotopocule measurements using laser spectroscopy: analyzer characterization and intercomparison
For the past two decades, the measurement of nitrous oxide (N2O) isotopocules – isotopically substituted molecules NNO, NNO and NNO of the main isotopic species NNO – has been a promising technique for understanding N2O production and consumption pathways. The coupling of non-cryogenic and tuneable light sources with different detection schemes, such as direct absorption quantum cascade laser absorption spectroscopy (QCLAS), cavity ring-down spectroscopy (CRDS) and off-axis integrated cavity output spectroscopy (OA-ICOS), has enabled the production of commercially available and field-deployable NO isotopic analyzers. In contrast to traditional isotope-ratio mass spectrometry (IRMS), these instruments are inherently selective for position-specific N substitution and provide real-time data, with minimal or no sample pretreatment, which is highly attractive for process studies.
Here, we compared the performance of NO isotope laser spectrometers with the three most common detection schemes: OA-ICOS (NOIA-30e-EP, ABB – Los Gatos Research Inc.), CRDS (G5131-i, Picarro Inc.) and QCLAS (dual QCLAS and preconcentration, trace gas extractor (TREX)-mini QCLAS, Aerodyne Research Inc.). For each instrument, the precision, drift and repeatability of NO mole fraction [NO] and isotope data were tested. The analyzers were then characterized for their dependence on [NO], gas matrix composition (O, Ar) and spectral interferences caused by HO, CO, CH and CO to develop analyzer-specific correction functions. Subsequently, a simulated two-end-member mixing experiment was used to compare the accuracy and repeatability of corrected and calibrated isotope measurements that could be acquired using the different laser spectrometers.
Our results show that NO isotope laser spectrometer performance is governed by an interplay between instrumental precision, drift, matrix effects and spectral interferences. To retrieve compatible and accurate results, it is necessary to include appropriate reference materials following the identical treatment (IT) principle during every measurement. Remaining differences between sample and reference gas compositions have to be corrected by applying analyzer-specific correction algorithms. These matrix and trace gas correction equations vary considerably according to NO mole fraction, complicating the procedure further. Thus, researchers should strive to minimize differences in composition between sample and reference gases. In closing, we provide a calibration workflow to guide researchers in the operation of NO isotope laser spectrometers in order to acquire accurate NO isotope analyses. We anticipate that this workflow will assist in applications where matrix and trace gas compositions vary considerably (e.g., laboratory incubations, NO liberated from wastewater or groundwater), as well as extend to future analyzer models and instruments focusing on isotopic species of other molecules
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