17 research outputs found

    Two-stage stochastic robust optimization scheduling of electric–thermal microgrid with solid electric thermal storage

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    During the periods of high heat load (HL) demand in winter, the increased heat output of combined heat and power units (CHPs) can significantly compress the electric power regulation range, thereby posing a threat to the safety of the power system. The solid electric thermal storage (SETS) can be employed as the regulating resource for both electric and thermal systems, expanding the dispatch space of microgrids to promote renewable energy consumption. In this paper, a two-stage stochastic robust optimization scheduling model of an electric–thermal microgrid with SETS is proposed, and the electric–thermal bi-directional regulation characteristics of SETS are considered. First, a SETS operation model based on the heat transfer characteristics of the homogeneous material-type thermal storage unit is established. Second, a regional thermal inertia model under a constant-flow variable-temperature system is established, which integrates HL at different locations to the heat source, avoiding the calculation of variation in water temperature, thus reducing the calculation difficulty. Finally, the two-stage stochastic robust optimization scheduling model of an electric–thermal microgrid with SETS is established. The model decouples the power and heat generation of CHP through the bi-directional regulation function of SETS. Case studies demonstrate the validity and effectiveness of the proposed scheduling model

    A Point-Scoring System for the Clinical Diagnosis of Sjögren's Syndrome Based on Quantified SPECT Imaging of Salivary Gland.

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    OBJECTIVE:To establish a point-scoring diagnostic system for Sjögren's syndrome (SS) based on quantified SPECT imaging of salivary gland, and evaluate its feasibility and performance compared with 2002 AECG criteria and 2012 ACR criteria. METHODS:213 patients with suspected SS enrolled in this study. The related clinical data of all patients were collected. All patients were evaluated and grouped on a clinical basis and posttreatment follow-up by rheumatology specialists as the unified standard (SS group with 149 cases and nSS group with 64 cases). From SPECT imaging of salivary gland, Tmax, UImax, Ts and EFs were derived for bilateral parotid and submandibular glands, and compared between the groups. A point-scoring diagnostic system for SS was established based on the quantified SPECT imaging of salivary gland. We estimated the sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV) and accuracy for the new diagnostic system, compared with 2002 AECG criteria and 2012 ACR criteria. RESULTS:When 7.0 was used as the cut-off point, the sensitivity, specificity, PPV, NPV and accuracy for the new point-scoring system in diagnosing SS were 89.93% (134/149), 93.75% (60/64), 97.10% (134/138), 80.00% (60/75) and 91.08% (194/213), respectively. The new point-scoring diagnostic system based on quantified SPECT imaging of salivary gland keeps the specificity comparatively to 2002 AECG criteria and 2012 ACR criteria, but improves the sensitivity significantly (P<0.01). CONCLUSION:The new point-scoring diagnostic system for SS based on quantified SPECT imaging of salivary gland may be superior to 2002 AECG criteria and 2012 ACR criteria, with higher sensitivity and similar specificity in the diagnosis of SS. Additionally, it also has good feasibility in the clinical settings

    Population genomics provides insights into the genetic basis of adaptive evolution in the mushroom-forming fungus Lentinula edodes.

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    IntroductionMushroom-forming fungi comprise diverse species that develop complex multicellular structures. In cultivated species, both ecological adaptation and artificial selection have driven genome evolution. However, little is known about the connections among genotype, phenotype and adaptation in mushroom-forming fungi.ObjectivesThis study aimed to (1) uncover the population structure and demographic history of Lentinula edodes, (2) dissect the genetic basis of adaptive evolution in L. edodes, and (3) determine if genes related to fruiting body development are involved in adaptive evolution.MethodsWe analyzed genomes and fruiting body-related traits (FBRTs) in 133 L. edodes strains and conducted RNA-seq analysis of fruiting body development in the YS69 strain. Combined methods of genomic scan for divergence, genome-wide association studies (GWAS), and RNA-seq were used to dissect the genetic basis of adaptive evolution.ResultsWe detected three distinct subgroups of L. edodes via single nucleotide polymorphisms, which showed robust phenotypic and temperature response differentiation and correlation with geographical distribution. Demographic history inference suggests that the subgroups diverged 36,871 generations ago. Moreover, L. edodes cultivars in China may have originated from the vicinity of Northeast China. A total of 942 genes were found to be related to genetic divergence by genomic scan, and 719 genes were identified to be candidates underlying FBRTs by GWAS. Integrating results of genomic scan and GWAS, 80 genes were detected to be related to phenotypic differentiation. A total of 364 genes related to fruiting body development were involved in genetic divergence and phenotypic differentiation.ConclusionAdaptation to the local environment, especially temperature, triggered genetic divergence and phenotypic differentiation of L. edodes. A general model for genetic divergence and phenotypic differentiation during adaptive evolution in L. edodes, which involves in signal perception and transduction, transcriptional regulation, and fruiting body morphogenesis, was also integrated here

    Regions of interest (ROIs) in SPECT imaging of salivary gland (SSG).

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    <p>The images of bilateral parotid and submandibular glands at 14min postinjection of radiotracer in the left panel (a). The time-activity curves for right parotid gland (red), left parotid gland (green), right submandibular gland (yellow) and left submandibular gland (blue) in the right panel (b).</p
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