Integrating work into life helps reduce residential greenhouse gas emissions.

Work from home (WFH) creates work-life integration by moving work into traditional life at home, but its influence on residential greenhouse gas (GHG) emissions remains unclear. In this study, an activity-based bottom-up model was developed to analyze the time-use patterns (activity durations and timeline of a typical day) of participants under WFH and traditional home life and to quantify their residential GHG emissions. Under WFH, participants generated an average of 9.03 kg CO2e/person/day, primarily attributed to space heating and cooling, cooking, grooming, work, and watching TV and movies. Notably, the GHG footprints varied across groups (8.08-9.93 kg CO2e/person/day) due to different work and household responsibilities and leisure time and varied with climate region (4.99-10.63 kg CO2e/person/day) because of emission factors of electricity, space heating and cooling, and cooking. Compared with traditional life at home (10.06 kg CO2e/person/day), WFH participants spent less time on almost all major activities (especially sleeping and watching TV and movies) to focus on work, enabling an 11.34% (1.02 kg CO2e/person/day) mitigation of GHG emissions. The reductions also varied by group and climate region, mainly associated with laundry, cooking, and watching TV and movies. Opportunities to reduce GHG emissions under WFH lie in targeting key activities, balancing the time spent on various activities, and developing group- and spatial-specific strategies. This study provides a systematic and high-resolution estimation of residential GHG emissions under WFH and traditional home life, with a complete system boundary, activity-specific considerations, and countrywide understanding. The findings reveal the environmental impact of work-life integration from the residential perspective and can aid residents and policymakers in utilizing decarbonization opportunities to advance low-carbon living under WFH.

Controllable adhesion behavior in underwater environments.

Microstructure adhesive pads can effectively manipulate objects in underwater environments. Current adhesive pads can achieve adhesion and separation with rigid substrates underwater; however, challenges remain in the control of adhesion and detachment of flexible materials. Additionally, underwater object manipulation necessitates considerable pre-pressure and is sensitive to water temperature fluctuations, potentially causing object damage and complicating adhesion and detachment processes. Thus, we present a novel, controllable adhesive pad inspired by the functional attributes of microwedge adhesive pads, combined with a mussel-inspired copolymer (MAPMC). In the context of underwater applications for flexible materials, the use of a microstructure adhesion pad with microwedge characteristics (MAPMCs) is a proficient approach to adhesion and detachment operations. This innovative method relies on the precise manipulation of the microwedge structure's collapse and recovery during its operation, which serves as the foundation for its efficacy in such environments. MAPMCs exhibit self-recovering elasticity, water flow interaction, and tunable underwater adhesion and detachment. Numerical simulations elucidate the synergistic effects of MAPMCs, highlighting the advantages of the microwedge structure for controllable, non-damaging adhesion and separation processes. The integration of MAPMCs into a gripping mechanism allows for the handling of diverse objects in underwater environments. Furthermore, by merging MAPMCs and a gripper within a linked system, our approach enables automatic, non-damaging adhesion, manipulation, and release of a soft jellyfish model. The experimental results indicate the potential applicability of MACMPs in underwater operations.

Effects of Zinc Smelting Waste Slag Treated with Root Organic Acids on the Liver of Zebrafish (Danio rerio).

Vegetation reconstruction was widely adopted for the waste slag site. But the toxic elements may be made public from slag due to the organic acid secreted by plant roots, which will pollute the surrounding environment and harm human health. The purpose of the study was to evaluate the harm of toxic substances released from zinc (Zn) smelting waste slag to zebrafish. The effect was simulated by adding organic acid to slag, and the toxicity of the slag was evaluated through the enzyme activity, genetic toxicity, tissue sections of zebrafish liver tissue. The results showed that more heavy metals were made public from the slag, as the concentration of organic acids increased. Exposure to toxic substances for 14 days, the antioxidant enzyme activities, termed as superoxide dismutase (SOD) and catalase (CAT), were significantly affected, which caused obvious malondialdehyde (MDA) accumulation. A comet assay revealed dose-dependent DNA damage in hepatocytes. Depending on the histopathological analysis, atrophy and necrosis of cells and increased hepatic plate gap were observed. The obtained results highlighted that toxic substances from slag may be deleterious to zebrafish.

YOLOH: You Only Look One Hourglass for Real-Time Object Detection.

Multi-scale detection based on Feature Pyramid Networks (FPN) has been a popular approach in object detection to improve accuracy. However, using multi-layer features in the decoder of FPN methods entails performing many convolution operations on high-resolution feature maps, which consumes significant computational resources. In this paper, we propose a novel perspective for FPN in which we directly use fused single-layer features for regression and classification. Our proposed model, You Only Look One Hourglass (YOLOH), fuses multiple feature maps into one feature map in the encoder. We then use dense connections and dilated residual blocks to expand the receptive field of the fused feature map. This output not only contains information from all the feature maps, but also has a multi-scale receptive field for detection. The experimental results on the COCO dataset demonstrate that YOLOH achieves higher accuracy and better run-time performance than established detector baselines, for instance, it achieves an average precision (AP) of 50.2 on a standard 3× training schedule and achieves 40.3 AP at a speed of 32 FPS on the ResNet-50 model. We anticipate that YOLOH can serve as a reference for researchers to design real-time detection in future studies. Our code is available at https://github.com/wsb853529465/YOLOH-main.

Intravenous administration of IL-12 encoding self-replicating RNA-lipid nanoparticle complex leads to safe and effective antitumor responses.

Interleukin 12 (IL-12) is a potent immunostimulatory cytokine mainly produced by antigen-presenting cells (e.g., dendritic cells, macrophages) and plays an important role in innate and adaptive immunity against cancers. Therapies that can synergistically modulate innate immunity and stimulate adaptive anti-tumor responses are of great interest for cancer immunotherapy. Here we investigated the lipid nanoparticle-encapsulated self-replicating RNA (srRNA) encoding IL-12 (referred to as JCXH-211) for the treatment of cancers. Both local (intratumoral) and systemic (intravenous) administration of JCXH-211 in tumor-bearing mice induced a high-level expression of IL-12 in tumor tissues, leading to modulation of tumor microenvironment and systemic activation of antitumor immunity. Particularly, JCXH-211 can inhibit the tumor-infiltration of polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs). When combined with anti-PD1 antibody, it was able to enhance the recruitment of T cells and NK cells into tumors. In multiple mouse solid tumor models, intravenous injection of JCXH-211 not only eradicated large preestablished tumors, but also induced protective immune memory that prevented the growth of rechallenged tumors. Finally, intravenous injection of JCXH-211 did not cause noticeable systemic toxicity in tumor-bearing mice and non-human primates. Thus, our study demonstrated the feasibility of intravenous administration of JCXH-211 for the treatment of advanced cancers.

Homeostatic Solid Solution Reaction in Phosphate Cathode: Breaking High-Voltage Barrier to Achieve High Energy Density and Long Life of Sodium-Ion Batteries.

The stable phase transformation during electrochemical progress drives extensive research on vanadium-based polyanions in sodium-ion batteries (SIBs), especially Na3V2(PO4)3 (NVP). And the electron transfer between V3+/4+ redox couple in NVP could be generally achieved, owing to the confined crystal variation during battery service. However, the more favorable V4+/5+ redox couple is still in hard-to-access situation due to the high barrier and further brings about the corresponding inefficiency in energy densities. In this work, the multilevel redox in NVP frame (MLNP) alters reaction pathway to undergo homeostatic solid solution process and breaks the high barrier of V4+/5+ at high voltage, taking by progressive transition metal (V, Fe, Ti, and Cr) redox couple. The diversified reaction paths across diffusion barriers could be realized by distinctive release/uptake of inactive Na1 site, confirmed by the calculations of density functional theory. Thereby its volume change is merely 1.73% during the multielectron-transfer process (≈2.77 electrons). MLNP cathode could achieve an impressive energy density of 440 Wh kg-1, driving the leading development of MLNP among other NASICON structure SIBs. The integration of multiple redox couples with low strain modulates the reaction pathway effectively and will open a new avenue for fabricating high-performance cathodes in SIBs.

Syntheses and structures of a series of uranyl phosphonates and sulfonates: an insight into their correlations and discrepancies.

Six uranyl phosphonates and sulfonates have been hydrothermally synthesized, namely, (H2tib)[(UO2)3(PO3C6H5)4]·2H2O (UPhP-1), Zn(pi)2(UO2)(PO3C6H5)2 (UPhP-2), Zn(dib)(UO2)(PO3C6H5)2·2H2O (UPhP-3), (HTEA)[(UO2)(5-SP)] (USP-1), (Hdib)2[(UO2)2(OH)(O)(5-SP)] (USP-2), and Zn(phen)3(UO2)2(3-SP)2 (USP-3) (tib = 1,3,5-tri(1H-imidazol-1-yl)benzene, pi = 1-phenyl-1H-imidazole, dib = 1,4-di(1H-imidazol-1-yl)benzene, TEA = triethylamine, phen = 1,10-phenanthroline, 5-SP = 5-sulfoisophthalic acid, and 3-SP = 3-sulfoisophthalic acid). UPhP-1 has been determined to be a layered structure constructed by UO7 pentagonal bipyramids, UO6 octahedra, and phenylphosphonates. Protonated tib plays a role in balancing the negative charge and holding its structure together. UPhP-2 is made up of UO6 octahedra, ZnO2N2 tetrahedra and PO3C tetrahedra in phenylphosphonates, forming a 1D assembly, which is stabilized by chelate phen ligand. Further connection of such chainlike structure via dib yields a 2D layered architecture of UPhP-3. Although sulfonate group possesses similar tetrahedral structure as the phosphonate group, a unidentated coordination mode is only found in this work. UO7 pentagonal bipyramids are linked by 5-SP to form the layered assembly of USP-1. USP-2 also consists of the same sulfonate ligand, but features tetranulear uranyl clusters. Similarly, protonated TEA and dib molecules enable stabilization of their structures, respectively. Formed by dinuclear uranyl cluster and 3-SP ligand, USP-3 appears as a 1D arrangement, in which Zn(phen)3 acts as the counterion to compensate the negative charge. All of these compounds have been characterized by IR and photoluminescent spectroscopy. Their characteristic emissions have been attributed as transition properties of uranyl cations.

Impact on the antioxidant system, histology, and cell death of zebrafish liver after exposure to industrial sludge leachate.

The improper disposal of sludge is a still-present phenomenon in China. The leachate formed at the bottom of the sludge pile would cause toxicological effects on aquatic organisms and affect the health of humans by entering the surrounding rivers and groundwater. In this study, the hepatotoxicity of zebrafish induced by sludge leachate was assessed by antioxidant enzyme activities, semi-quantitative histopathological assessment, and TUNEL apoptosis assay. The results indicated that the leachate would induce oxidative stress and eventually lead to an increase in lipid peroxide after a 7-day exposure. The histopathological indexes demonstrated that exposure to leachate would cause histological damage by circulatory disturbances, regressive changes, progressive changes, and inflammatory responses. According to the TUNEL results, it could be inferred that apoptotic hepatocytes increased after exposure for 7 days due to oxidative stress and histological damage. Overall, this study provided a valuable approach to assessing the toxic effects of sludge leachate and described the underlying mechanism of leachate-induced hepatotoxicity in zebrafish. This work will generate new insights into the ecological toxicity of leachate and promote the development of sludge disposal in China.

From 1D chain to 3D framework uranyl diphosphonates: syntheses, crystal structures, and selective ion exchange.

In this work, we demonstrate a family of new inorganic-organic hybrid uranyl diphosphonates based on 1-hydroxyethylidenediphosphonic acid (H(4)L) linker by using hydrothermal method. These compounds, (Hbpi)[(UO(2))(H(2)O)(HL)]·H(2)O (UP-1), represents 1D structure, (Hbpi)[(UO(2))(H(2)O)(HL)] (UP-2), (H(2)dib)(0.5)[(UO(2))(H(2)O)(HL)] (UP-3), and [(UO(2))(H(2)O)(H(2)L)]·2H(2)O (UP-4) feature 2D architectures, (H(2)bipy){[(UO(2))(H(2)O)](2)[(UO(2))(H(2)O)(2)](L)(2)}·2H(2)O (UP-5), and (H(3)O)(2){[(UO(2))(H(2)O)](3)(L)(2)}·2H(2)O (UP-6) adopt 3D networks (bpi: 1-(biphenyl-4-yl)-1H-imidazole, dib: 1,4-di(1H-imidazol-1-yl)benzene, bipy: 2,2'-bipyridine). Among them, UP-1, UP-2, UP-3, and UP-4 possess the same structural building unit but with different structures. UP-5 and UP-6 feature the same UO(2)/L ratio of 3:2 but a different structural building unit. Photoluminescence studies reveal that UP-5 displays characteristic emissions of uranyl cations. Ion-exchange experiments demonstrate that the H(3)O(+) in UP-6 can be easily and selectively exchanged by monovalent cations including Na(+), K(+), Cs(+), and Ag(+) cations, whereas the framework retains identical as confirmed by single-crystal X-ray diffractions.

3-Fold-interpenetrated uranium-organic frameworks: new strategy for rationally constructing three-dimensional uranyl organic materials.

The first series of 3-fold-interpenetrated uranium-organic frameworks, UOF-1 and UOF-2, have been synthesized by hydrothermal reactions of flexible semirigid carboxylic acids and uranyl nitrate. Structure analyses indicate that UOF-1 and UOF-2 possess flu and pts topologies, respectively.

Family Relationships Under Work From Home: Exploring the Role of Adaptive Processes.

Work-from-home (WFH) influences both work and life, and further impacts family relationships. The current study explored the impacts of WFH on family relationships during the COVID-19 pandemic and identified effective adaptive processes for maintaining family relationships under WFH. Using the Vulnerability-Stress-Adaptation (VSA) model, the study examined the roles of adaptive processes (spending time with family members and balancing work and life) and demographic differences (gender, age, marital status, and education level) in the relation between WFH and family relationships. Path analysis results based on an online survey (N = 150) suggested that, overall, WFH improved family relationships through proper adaptive processes. WFH had a positive relation to time spent with family members, and this relation was especially salient for workers with lower education levels. While there was no statistically significant overall relation between WFH and work-life balance, older workers tended to engage in increased work-life balance during WFH. Both adaptive processes were positively related to family relationship quality. The findings advance the understanding of family relationships and WFH and provide practical recommendations to enhance family relationships under WFH.

Discovery and Genomic Function of a Novel Rice Dwarf-Associated Bunya-like Virus.

Bunyaviruses cause diseases in vertebrates, arthropods, and plants. Here, we used high-throughput RNA-seq to identify a bunya-like virus in rice plants showing the dwarfing symptom, which was tentatively named rice dwarf-associated bunya-like virus (RDaBV). The RDaBV genome consists of L, M, and S segments. The L segment has 6562 nt, and encodes an RdRp with a conserved Bunya_RdRp super family domain. The M segment has 1667 nt and encodes a nonstructural protein (NS). The complementary strand of the 1120 nt S segment encodes a nucleocapsid protein (N), while its viral strand encodes a small nonstructural protein (NSs). The amino acid (aa) sequence identities of RdRp, NS, and N between RDaBV and viruses from the family Discoviridae were the highest. Surprisingly, the RDaBV NSs protein did not match any viral proteins. Phylogenetic analysis based on RdRp indicated that RDaBV is evolutionarily close to viruses in the family Discoviridae. The PVX-expressed system indicated that RDaBV N and NS may be symptom determinants of RDaBV. Our movement complementation and callose staining experiment results confirmed that RDaBV NSs is a viral movement protein in plants, while an agro-infiltration experiment found that RDaBV NS is an RNA silencing suppressor. Thus, we determined that RDaBV is a novel rice-infecting bunya-like virus.

Facile Method for Fabricating Microfluidic Chip Integrated with Microwell Arrays for Cell Trapping.

With the development of biomedical technology, personalized diagnosis and treatment at the single-cell level are becoming more important in the medical field. As one of the most powerful tools, microfluidic chips have shown significant potential for various applications related to cell separation, cell proliferation, and cell behavior analysis. However, fabricating microfluidic devices requires complicated procedures and high-cost equipment. In this study, an optofluidic maskless lithography method was proposed for rapid fabrication of microfluidic devices integrated with microwells. Through the use of this approach, microwells can be on-line designed and the exposure patterns can be modulated. Single or multi polystyrene microspheres were successfully trapped by using the designed microwells. The capture of MCF-7 cells and cell arrays indicated that the microfluidic devices fabricated in the present study can be applied for cell research.

Two-step synthesis of hole structure bastnasite (RECO3F RE = Ce, La, Pr, Nd) sub-microcrystals with tunable luminescence properties.

A two-step synthetic route using RE(OH)CO3 colloid spheres as the sacrificial template was designed to prepare monodisperse, pure bastnasite (RECO3F: RE = Ce, La, Pr, Nd) with a hole structure for the first time. A variety of morphologies, including jujube core-like, stacked nanoblocks, and stacked nanosheets were obtained through changing the ratio of reactants. The phase, structure, shapes, and photoluminescence properties of samples were characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM) and photoluminescence (PL) spectroscopy. The CeCO3F:Ln3+ (Ln = Tb, Eu, Dy) phosphors give green, yellow and blue emission, respectively, due to the f-f transitions of Ln3+ ions. Furthermore, the energy transfer from Ce3+ to Dy3+ and Tb3+ was described in detail.

A novel color-tunable phosphor, Na5Gd9F32:Ln3+ (Ln = Eu, Tb, Dy, Sm, Ho) sub-microcrystals: structure, luminescence and energy transfer properties.

Ln3+-Doped fluorides are economical and highly efficient luminescent materials, which play a crucial role in LEDs, biolabeling, and sensors. Therefore, Na5Gd9F32:Ln3+ sub-microspheres with tunable multicolor emissions were successfully synthesized via a simple water bath method employing colloidal Gd(OH)CO3 spheres as precursors. Samples were characterized by XRD, SEM, TEM, EDS and PL. It was found that the hydrolysis of BF4- ions had a dynamic effect on the retention of the morphology of the product owing to the mild reaction environment caused by the low hydrolysis rate of BF4- ions. Upon excitation by ultraviolet light, the Na5Gd9F32:Ln3+ (Ln = Eu, Tb, Dy, Sm, Ho) phosphors underwent characteristic f-f transitions and gave rise to red, green, green, yellow, and pale green emissions, respectively. Moreover, various emission colors could be obtained by using different excitation wavelengths and adjusting the Eu3+/Tb3+ molar ratio owing to energy transfer between Tb3+ and Eu3+ ions in the Na5Gd9F32 host. The energy transfer mechanism was demonstrated to be a dipole-dipole interaction. The multicolor luminescent phosphors with a certain dopant concentration based on a single host and excitation wavelength may have potential applications in the field of lighting displays.