248 research outputs found
Optimization of the Front-end Logistics Routes of Agricultural Products Based on Network Platform
Aiming to promote the effective connection between the individual farmers and the modern “big market” and improve the logistics efficiency of agricultural products, this paper offers a logistics model for decentralized production to achieve organized information and large-scaled transportation. Based on the in-depth analysis of the traditional agricultural product logistics chain, this paper originates a network logistics model for agricultural products. It constructs a two-stage framework (grouping first and then scheduling), analyzes the “First Mile” logistics routes, and then uses the improved loop routes optimization algorithm to obtain the approximate optimal solution to the model. Through example verification, it is found that the model can help improve the efficiency of logistics distribution and save the logistics costs of small agricultural products from fragmented land. Moreover, the results show that the agricultural product logistics method based on overall transportation and information management is obviously superior to the traditional logistics methods
Analysis on the Correlation Degree between the Driver’s Reaction Ability and Physiological Parameters
In this paper, the correlation degree between driver’s reaction time and the physiological signal is analyzed. For this purpose, a large number of road experiments are performed using the biopac and the reaction time test systems to collect data. First, the electroencephalograph (EEG) signal is processed by using the fast Fourier and the inverse Fourier transforms. Then, the power spectrum densities (PSD) of α, β, δ, and EEG wave are calculated by Welch procedure. The average power of the power spectrum of α, β, and θ is calculated by the biopac software and two ratio formulas, (α+θ)/β and α/β, are selected to be the impact factors. After that the heart rate and the standard deviation of RR interval are calculated from the electrocardiograph (ECG) signal. Lastly, the correlation degree between the eight impact factors and the reaction time are analyzed based on the grey correlation analysis. The results demonstrate that α/β has the greatest correlation to the reaction time except EEG-PSD. Furthermore, two mathematical models for the reaction time-driving time and the α/β-driving time are developed based on the Gaussian function. These mathematical models are then finally used to establish the functional relation of α/β-the reaction time
MaxCyte scalable electroporation: A universal cell engineering platform for development of cell-based medicines from R&D to clinic
Each cell-based therapeutic modality – from viral vectors to immune cell engineering and in situ gene editing – relies on different biologic approaches, however, they all require some type of cell engineering therapeutic manufacturing. MaxCyte developed a non-viral, electroporation-based cell engineering technology that has the performance, flexibility, safety and scalability for use in cell therapy development through to manufacturing for patient treatment. In this poster, we present capabilities of MaxCyte scalable electroporation, a platform of cGMP-compliant, CE-marked instruments with an FDA Master File. Data for high performance electroporation of a variety of cell types commonly used in cellular therapeutics, including adherent and suspension cells as well as cell lines and primary cells, are summarized. Use of MaxCyte electroporation for a breadth of real world applications are highlighted including lentivirus and AAV production, engineering of primary T-cells for the expression of an anti-mesothelin CAR molecule, and CRISPR-mediate gene editing of stem cells. These data will directly illustrate the scalability and consistency of MaxCyte electroporation that enables the use of this single cell engineering technology from early R&D to patient dosing of cell-based biotherapeutics
Tuning the emission properties of a fluorescent polymer using a polymer microarray approach - identification of an optothermo responsive polymer
Fluorescent polymer microarrays were prepared using inkjet printing and screened. The fluorescence intensity was found to be tunable by temperature change when the dye was immobilized in identified thermo-responsive polymer beads.</p
Geographical variation and correlates of tobacco smoking, second-hand smoke exposure, workplace tobacco prohibition, and pro-tobacco and counter-tobacco advertising in mainland China: a cross-sectional study of 98 058 participants
Abstract presented at The Lancet-CAMS Health Summit, 30-31 October 2015, Beijing, Chin
Driver distraction detection based on lightweight networks and tiny object detection
Real-time and efficient driver distraction detection is of great importance for road traffic safety and assisted driving. The design of a real-time lightweight model is crucial for in-vehicle edge devices that have limited computational resources. However, most existing approaches focus on lighter and more efficient architectures, ignoring the cost of losing tiny target detection performance that comes with lightweighting. In this paper, we present MTNet, a lightweight detector for driver distraction detection scenarios. MTNet consists of a multidimensional adaptive feature extraction block, a lightweight feature fusion block and utilizes the IoU-NWD weighted loss function, all while considering the accuracy gain of tiny target detection. In the feature extraction component, a lightweight backbone network is employed in conjunction with four attention mechanisms strategically integrated across the kernel space. This approach enhances the performance limits of the lightweight network. The lightweight feature fusion module is designed to reduce computational complexity and memory access. The interaction of channel information is improved through the use of lightweight arithmetic techniques. Additionally, CFSM module and EPIEM module are employed to minimize redundant feature map computations and strike a better balance between model weights and accuracy. Finally, the IoU-NWD weighted loss function is formulated to enable more effective detection of tiny targets. We assess the performance of the proposed method on the LDDB benchmark. The experimental results demonstrate that our proposed method outperforms multiple advanced detection models
Diversity of endosymbionts in camellia spiny whitefly, Aleurocanthus camelliae (Hemiptera: Aleyrodidae), estimated by 16S rRNA analysis and their biological implications
Camellia spiny whitefly, Aleurocanthus camelliae (Hemiptera: Aleyrodidae), is a major pest in tea, which poses a serious threat to tea production. Similar to many insects, various bacterial symbioses inside A. camelliae may participate in the reproduction, metabolism, and detoxification of the host. However, few reports included research on the microbial composition and influence on A. camelliae growth. We first applied high-throughput sequencing of the V4 region in the 16S rRNA of symbiotic bacteria to study its component and effect on the biological trait of A. camelliae by comparing it with the antibiotic treatment group. The population parameters, survival rate, and fecundity rate of A. camelliae were also analyzed using the age–stage two-sex life table. Our results demonstrated that phylum Proteobacteria (higher than 96.15%) dominated the whole life cycle of A. camelliae. It unveiled the presence of Candidatus Portiera (primary endosymbiont) (67.15–73.33%), Arsenophonus (5.58–22.89%), Wolbachia (4.53–11.58%), Rickettsia (0.75–2.59%), and Pseudomonas (0.99–1.88%) genus. Antibiotic treatment caused a significant decrease in the endosymbiont, which negatively affected the host's biological properties and life process. For example, 1.5% rifampicin treatment caused a longer preadult stage in the offspring generation (55.92 d) compared to the control (49.75d) and a lower survival rate (0.36) than the control (0.60). The decreased intrinsic rate of increase (r), net reproductive rate (R0), and prolonged mean generation time (T) were signs of all disadvantageous effects associated with symbiotic reduction. Our findings confirmed the composition and richness of symbiotic bacteria in larva and adult of A. camelliae by an Illumina NovaSeq 6000 analysis and their influence on the development of the host by demographic research. Together, the results suggested that symbiotic bacteria play an important role in manipulating the biological development of their hosts, which might help us for developing new pest control agents and technologies for better management of A. camelliae
Stiffness of Substrate Influences the Distribution but not the Synthesis of Autophagosomes in Human Liver (LO2) Cells
Extracellular matrix (ECM) often becomes stiffer during tumor development, which not only gives the tumor's hardness feel but also actively contributes to the tumor formation. A good example is hepatocellular carcinoma (HCC) that usually develops within chronically stiffened liver tissues due to fibrosis and cirrhosis. On the other hand, HCC cells exhibit reduced autophagy in a malignancy dependent manner, suggesting autophagy is suppressed during tumor development. However, it is not known whether ECM stiffness would influence autophagy during tumor development. To investigate this issue, We cultured the human liver (LO2) cells that stably expressed autophagosome indicator LC3 on polydimethylsiloxane (PDMS) gels with stiffness varying from 11 to 1220 kPa. and on plastic cell culture dish as controls for up to 48h. We found that the total protein level of LC3-II in LO2 cells was not affected by the substrate stiffness. However the autophagosomes in LO2 cells cultured on the soft substrate (11 kPa PDMS gel) were localized and accumulated around the nucleus, while those on the stiff substrate (1220 kPa PDMS gel or plastic dish surface) were dispersed throughout the cytoplasmic space. Therefore, our data suggest that ECM stiffness may not directly synthesize nascent autophagosomes, but instead influence the location/translocation and ultimately distribution of autophagosomes in the cells
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