Correction: Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways.

[This corrects the article DOI: 10.1371/journal.pgen.1009233.].

Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways.

Runx1 is highly expressed in osteoblasts, however, its function in osteogenesis is unclear. We generated mesenchymal progenitor-specific (Runx1f/fTwist2-Cre) and osteoblast-specific (Runx1f/fCol1α1-Cre) conditional knockout (Runx1 CKO) mice. The mutant CKO mice with normal skeletal development displayed a severe osteoporosis phenotype at postnatal and adult stages. Runx1 CKO resulted in decreased osteogenesis and increased adipogenesis. RNA-sequencing analysis, Western blot, and qPCR validation of Runx1 CKO samples showed that Runx1 regulates BMP signaling pathway and Wnt/ß-catenin signaling pathway. ChIP assay revealed direct binding of Runx1 to the promoter regions of Bmp7, Alk3, and Atf4, and promoter mapping demonstrated that Runx1 upregulates their promoter activity through the binding regions. Bmp7 overexpression rescued Alk3, Runx2, and Atf4 expression in Runx1-deficient BMSCs. Runx2 expression was decreased while Runx1 was not changed in Alk3 deficient osteoblasts. Atf4 overexpression in Runx1-deficient BMSCs did not rescue expression of Runx1, Bmp7, and Alk3. Smad1/5/8 activity was vitally reduced in Runx1 CKO cells, indicating Runx1 positively regulates the Bmp7/Alk3/Smad1/5/8/Runx2/ATF4 signaling pathway. Notably, Runx1 overexpression in Runx2-/- osteoblasts rescued expression of Atf4, OCN, and ALP to compensate Runx2 function. Runx1 CKO mice at various osteoblast differentiation stages reduced Wnt signaling and caused high expression of C/ebpα and Pparγ and largely increased adipogenesis. Co-culture of Runx1-deficient and wild-type cells demonstrated that Runx1 regulates osteoblast-adipocyte lineage commitment both cell-autonomously and non-autonomously. Notably, Runx1 overexpression rescued bone loss in OVX-induced osteoporosis. This study focused on the role of Runx1 in different cell populations with regards to BMP and Wnt signaling pathways and in the interacting network underlying bone homeostasis as well as adipogenesis, and has provided new insight and advancement of knowledge in skeletal development. Collectively, Runx1 maintains adult bone homeostasis from bone loss though up-regulating Bmp7/Alk3/Smad1/5/8/Runx2/ATF4 and WNT/ß-Catenin signaling pathways, and targeting Runx1 potentially leads to novel therapeutics for osteoporosis.

Monotropein Protects Mesenchymal Stem Cells from Lipopolysaccharide-Induced Impairments and Promotes Fracture Healing in an Ovariectomized Mouse Model.

Monotropein is one of the active ingredients in Morinda Officinalis, which has been used for the treatment in multiple bone and joint diseases. This study aimed to observe the in vitro effects of Monotropein on osteogenic differentiation of lipopolysaccharide treated bone marrow mesenchymal stem cells (bMSCs), and the in vivo effects of local application of Monotropein on bone fracture healing in ovariectomized mice. Lipopolysaccharide was used to set up the inflammatory model in bMSCs, which were treated by Monotropein. Molecular docking analysis was performed to evaluate the potential interaction between Monotropein and p65. Transverse fractures of middle tibias were established in ovariectomized mice, and Monotropein was locally applied to the fracture site using injectable hydrogel. Monotropein enhanced the ability of primary bMSCs in chondro-osteogenic differentiation. Furthermore, Monotropein rescued lipopolysaccharide-induced osteogenic differentiation impairment and inhibited lipopolysaccharide-induced p65 phosphorylation in primary bMSCs. Docking analysis showed that the binding activity of Monotropein and p65/14-3-3 complex is stronger than the selective inhibitor of NF-κB (p65), DP-005. Local application of Monotropein partially rescued the decreased bone mass and biomechanical properties of callus or healed tibias in ovariectomized mice. The expressions of Runx2, Osterix and Collagen I in the 2-week callus were partially restored in Monotropein-treated ovariectomized mice. Taking together, local application of Monotropein promoted fracture healing in ovariectomized mice. Inhibition of p65 phosphorylation and enhancement in osteogenesis of mesenchymal stem cells could be partial of the effective mechanisms.

Photodissociation Dynamics of the [O2-H2O]+ Ionic Complex.

We present an experimental study on the photodissociation dynamics of [O2-H2O]+ in the 580-266 nm wavelength range using a cryogenic ion trap velocity map imaging spectrometer. The cryogenic ion trap produces mass selected and internally cold [O2-H2O]+ ions for photodissociation. By detecting both the O2+ and H2O+ photofragments using the time-of-flight mass spectrometry and velocity map imaging techniques, branching ratios and total kinetic energy release distributions of the O2+ + H2O and H2O+ + O2 product channels are experimentally measured at 16 different excitation energies. State-resolved photodissociation mechanisms of the parent [O2-H2O]+ are interpreted as (1) the O2(X3Σg-) + H2O+(X~2B1), O2(a1Δg) + H2O+(X~2B1), and O2(X3Σg-) + H2O+(A~2A1) channels are produced from direct dissociation of [O2-H2O]+ in its excited B~2A″, D~2A″, and F~2A″ states, respectively; (2) the O2+(X2Πg) + H2O(X~A11) channel is produced from nonadiabatic relaxations of the excited B~2A″, D~2A″, and F~2A″ states to the X~2A″ ground state with subsequent dissociation. The latter nonadiabatic processes involve charge-transfer on the potential energy surfaces, and the charge-transfer probabilities are determined from experimental results. The dissociation energy of the ground state to the lowest dissociation limit is experimentally refined as D0 = 1.05 ± 0.05 eV. This work provides important information to understand the charge-transfer dynamics in the photochemistry of [O2-H2O]+ and in the ion-molecule reaction O2 + H2O+ → O2+ + H2O.

Quantum Key Distribution over 658 km Fiber with Distributed Vibration Sensing.

Twin-field quantum key distribution (TFQKD) promises ultralong secure key distribution which surpasses the rate distance limit and can reduce the number of the trusted nodes in long-haul quantum network. Tremendous efforts have been made toward implementation of TFQKD, among which, the secure key with finite size analysis can distribute more than 500 km in the lab and in the field. Here, we demonstrate the sending-or-not-sending TFQKD experimentally, achieving a secure key distribution with finite size analysis over a 658 km ultra-low-loss optical fiber. Meanwhile, in a TFQKD system, any phase fluctuation due to temperature variation and ambient variation during the channel must be recorded and compensated, and all this phase information can then be utilized to sense the channel vibration perturbations. With our quantum key distribution system, we recovered the external vibrational perturbations generated by artificial vibroseis on both the quantum and frequency calibration link, and successfully located the perturbation position in the frequency calibration fiber with a resolution better than 1 km. Our results not only set a new distance record of quantum key distribution, but also demonstrate that the redundant information of TFQKD can be used for remote sensing of the channel vibration, which can find applications in earthquake detection and landslide monitoring besides secure communication.

High-Resolution Electronic Spectrum of the 1,4,6-Heptatrienyl Radical in the Gas Phase.

We report the gas-phase identification of the 1,4,6-heptatrienyl (C7H9) radical via its A~2B1-X~2A2 electronic transition spectrum. The optical absorption spectrum in the 590-630 nm region is recorded using cavity ring-down spectroscopy in combination with a supersonic plasma jet. An analysis of the rotationally resolved 000 origin band spectrum has allowed an accurate determination of spectroscopic constants for both the X~2A2 electronic ground and A~2B1 excited states of this radical. Ab initio calculations at the CASPT2/cc-pVTZ level have been performed to predict the radical structure and molecular constants that are in good agreement with the experimental results. By combination with available experimental data for the allyl and 1,4-pentadienyl radicals, we extrapolate an excitation energy gap between the ground and first excited states of a long C2n-1H2n+1 polyenyl chain converging to a residual energy gap, suggesting the presence of residual nonuniform C-C bond lengths in a long polyenyl chain.

Gas-Phase Optical Spectra of the Indenyl Radical and Its Quantitative Detection in a Jet-Stirred Reactor.

Resonance-stabilized radicals (RSRs), such as the indenyl radical (C9H7), are proposed to be initiator radicals in soot inception and growth in hydrocarbon combustion processes, but spectroscopic data for many RSRs are still lacking. In this work, the gas-phase optical absorption spectra of the B̃2A2-X̃2A2 electronic transition of indenyl were identified in a supersonic indene/argon plasma jet. Spectroscopic parameters, including the transition energy, rotational constants, and upper-state lifetime broadening, were obtained from analysis of the experimental spectra. The results were readily applied to the quantitative detection of indenyl produced from high-temperature reactions in a jet-stirred reactor. This study now makes indenyl optically accessible in further reaction kinetics studies and in situ spectroscopic diagnostics of hydrocarbon combustion processes.

High-resolution laser spectroscopy of the trans- and cis-1-vinylpropargyl radicals.

Rotationally resolved spectra of the Ã2A''-X̃2A'' origin bands for both trans- and cis-conformers of 1-vinylpropargyl radical (1VPR) are experimentally studied. Rotational constants for both ground and electronically excited states are experimentally determined. The stability of the Ã2A'' excited state of the cis-1VPR is found to be higher than that of trans-1VPR, which is likely due to additional π-overlap and increased pπ electron delocalization in the excited state of cis-1VPR.

Comparative lifecycle greenhouse gas emissions and their reduction potential for typical petrochemical enterprises in China.

Petrochemical enterprises have become a major source of global greenhouse gas (GHG) emissions. Yet, due to the unavailability of basic data, there is still a lack of case studies to quantify GHG emissions and provide petrochemical enterprises with guidelines for implementing energy conservation and emission reduction strategies. Therefore, this study conducted a life cycle assessment (LCA) analysis to estimate the GHG emissions of four typical petrochemical enterprises in China, using first-hand data, to determine possible emission reduction measures. The analytical data revealed that Dushanzi Petrochemical (DSP) has the highest GHG emission intensity (1.17 tons CO2e/ton), followed by Urumqi Petrochemical (UP) (1.08 tons CO2e/ton), Dalian Petrochemical (DLP) (average 0.58 tons CO2e/ton) and Karamay Petrochemical (KP) (average 0.50 tons CO2e/ton) over the whole life cycle. At the same time, GHG emissions during fossil fuel combustion were the largest contributor to the whole life cycle, accounting for about 77.31%-94.27% of the total emissions. In the fossil-fuel combustion phase, DSP had the highest unit GHG emissions (1.20 tons CO2e), followed by UP (0.89 tons CO2e). In the industrial production phase, DLP had the highest unit GHG emissions (average 0.13 tons CO2e/ton), followed by UP (0.10 tons CO2e/ton). During the torch burning phase, torch burning under accident conditions was the main source of GHG emissions. It is worth noting that the CO2 recovery stage has "negative value," indicating that it will bring some environmental benefits. Further scenario analysis shows that effective policies and advanced technologies can further reduce GHG emissions.

The RBG-1-RBG-2 complex modulates autophagy activity by regulating lysosomal biogenesis and function in C. elegans.

Vici syndrome is a severe and progressive multisystem disease caused by mutations in the EPG5 gene. In patient tissues and animal models, loss of EPG5 function is associated with defective autophagy caused by accumulation of non-degradative autolysosomes, but very little is known about the mechanism underlying this cellular phenotype. Here, we demonstrate that loss of function of the RBG-1-RBG-2 complex ameliorates the autophagy defect in C. elegansepg-5 mutants. The suppression effect is independent of the complex's activity as a RAB-3 GAP and a RAB-18 GEF. Loss of rbg-1 activity promotes lysosomal biogenesis and function, and also suppresses the accumulation of non-functional autolysosomes in epg-5 mutants. The mobility of late endosome- and lysosome-associated RAB-7 is reduced in epg-5 mutants, and this defect is rescued by simultaneous loss of function of rbg-1 Expression of the GDP-bound form of RAB-7 also promotes lysosomal biogenesis and suppresses the autophagy defect in epg-5 mutants. Our study reveals that the RBG-1-RBG-2 complex acts by modulating the dynamics of membrane-associated RAB-7 to regulate lysosomal biogenesis, and provides insights into the pathogenesis of Vici syndrome.

Changes in macrophage and inflammatory cytokine expressions during fracture healing in an ovariectomized mice model.

BACKGROUND: Macrophages and inflammatory cytokines play important roles in bone fracture healing. However, the expression patterns of macrophages and inflammatory cytokines during fracture healing under the condition of postmenopausal osteoporosis have not been fully revealed. METHODS: Tibia transverse fracture was established 12 weeks after ovariectomy or sham operation in 16-week old female mice. Tibias were harvested before fracture or 1, 3, 5, 7, 14, 21, 28 days after fracture for radiological and histological examinations. M1/M2 inflammatory macrophages, osteal macrophages and gene expressions of tumor necrosis factor-α, interleukin-6, interleukin-1ß and macrophage conversion related molecules in the fracture haematoma or callus were also detected. RESULTS: The processes of fracture healing, especially the phases of endochondral ossification and callus remodeling, were delayed in ovariectomized mice. The expressions of tumor necrosis factor-α and interleukin-6, but not interleukin-1ß, in the fracture haematoma or callus were disturbed. Expressions of tumor necrosis factor-α were decreased at 1, 14 and 21 days post-fracture (DPF), and were increased at 3, 5 and 7 DPF. Interleukin-6 expressions at 1, 3 and 21 DPF were significantly increased. We found the decreases in M1 and M2 macrophages at 1 DPF of the initial inflammatory stage. M2 macrophages at 14 DPF of the middle stage and osteal macrophages at 14, 21 and 28 DPF of the middle and late stages of fracture healing were also reduced in ovariectomized mice. CONCLUSIONS: The expressions of macrophages and inflammatory cytokines were impaired in ovariectomized mice, which might contribute partially to poor fracture healing.

Oleanolic acid exerts inhibitory effects on the late stage of osteoclastogenesis and prevents bone loss in osteoprotegerin knockout mice.

Postmenopausal women undergo rapid bone loss, which caused by the accelerated osteoclastic bone resorption. Receptor activator of nuclear factor kappa-B ligand (RANKL) plays critical and essential roles on varied stages of osteoclastogenesis. Oleanolic acid (OA), a naturally derived small compound, has been found suppress osteoclastogenesis in early stage of bone marrow macrophages (BMMs). However, whether OA also regulates the late stage of osteoclastogenesis remains unclear. Here, the regulatory effect of OA on the late stage of osteoclastogenesis was investigated in vitro using RANKL-pretreated BMMs and in vivo using osteoprotegerin (OPG) knockout mice. Our in vitro studies demonstrate that OA inhibits the late stage of osteoclastogenesis from RANKL-pretreated BMMs. For in vivo animal investigation, OA attenuates the bone loss phenotypes in OPG-knockout mice by decreasing the densities of osteoclast, which are in consistent with the finding with in vitro osteoclastogenesis. Mechanistic investigations found that OA largely inhibit the activity of c-Fos and Nuclear factor of activated T-cells c1 (NFATc1) with RANKL-pretreated BMMs and OPG-knockout mice. Furthermore, OA suppresses the activities of osteoclast genes, such as Tartrate resistant acid phosphatase (TRAP), CathepsinK (Ctsk), and Matrix metalloproteinase 9 (MMP9). Taken together these findings, they have not only defined an inhibitory effect of OA in the late stage of osteoclastogenesis but have also gained new molecular mechanisms underlying the process of osteoclast formation.

High-Resolution Laser Spectroscopic Survey of the H3Σu--X3Σg- Electronic Transition of Si2.

Rotationally resolved spectra of the H3Σu--X3Σg- electronic transition bands of Si2 have been experimentally studied using laser-induced fluorescence in the 380-520 nm range. Si2 molecules are produced in a supersonically expanding planar plasma by discharging a silane/argon gas mixture. In total, 44 bands belonging to the H3Σu--X3Σg- electronic transition system of the most abundant isotopologue 28Si2 are experimentally recorded. With a spectral resolution of ∼0.04 cm-1, the triplet spin-splitting structures in individual rotational transition lines are fully resolved. Detailed analyses on the high-resolution spectra have yielded an accurate determination of spectroscopic constants for both X3Σg- and H3Σu- states. The spin-spin interaction constants for the two triplet states are found to be comparable (λ ≈1.5 cm-1), which may originate from the 3p atomic orbital interaction in the triplet Si2 molecule. The measured isotopologue spectra of 29Si28Si and 30Si28Si indicate that the H3Σu--X3Σg- transition system of 29S28S and 30S28S can be reasonably reproduced by the isotope mass-scaling rule. Spectroscopic parameters, including the Franck-Condon factors, the Einstein coefficients, and the oscillator strengths, are also determined from the experimental results and the Rydberg-Klein-Rees (RKR) calculations. The agreement between the experimentally measured and calculated dispersed fluorescence spectra indicates that the RKR calculations with the molecular constants determined in this work can accurately reproduce the diatomic potentials of both states. These molecular data provide a benchmark in high-level theoretical studies on Si2 and likely other small silicon clusters.

Dissociation dynamics of carbon dioxide cation (CO2 +) in the C2Σg + state via [1+1] two-photon excitation.

The dissociation dynamics of CO2 + in the C2Σg + state has been studied in the 8.14-8.68 eV region by [1+1] two-photon excitation via vibronically selected intermediate A2Πu and B2Σu + states using a cryogenic ion trap velocity map imaging spectrometer. The cryogenic ion trap produces an internally cold mass selected ion sample of CO2 +. Total translational energy release (TER) and two-dimensional recoiling velocity distributions of fragmented CO+ ions are measured by time-sliced velocity map imaging. High resolution TER spectra allow us to identify and assign three dissociation channels of CO2 + (C2Σg +) in the studied energy region: (1) production of CO+(X2Σ+) + O(3P) by predissociation via spin-orbit coupling with the repulsive 14Πu state; (2) production of CO+(X2Σ+) + O(1D) by predissociation via bending and/or anti-symmetric stretching mediated conical intersection crossing with A2Πu or B2Σu +, where the C2Σg +/A2Πu crossing is considered to be more likely; (3) direct dissociation to CO+(A2Π) + O(3P) on the C2Σg + state surface, which exhibits a competitive intensity above its dissociation limit (8.20 eV). For the first dissociation channel, the fragmented CO+(X2Σ+) ions are found to have widely spread populations of both rotational and vibrational levels, indicating that bending of the parent CO2 + over a broad range is involved upon dissociation, while for the latter two channels, the produced CO+(X2Σ+) and CO+(A2Π) ions have relatively narrow rotational populations. The anisotropy parameters ß are also measured for all three channels and are found to be nearly independent of the vibronically selected intermediate states, likely due to complicated intramolecular interactions in the studied energy region.

Combined experimental and theoretical study on the ultraviolet photodissociation dynamics of 1-bromo-2,6-difluorobenzene in 267 nm-234 nm.

Thanks to their specific molecular symmetry, aromatic molecules and their derivatives represent ideal model systems in understanding photo-induced chemistry of small molecules. Herein, ultraviolet photodissociation dynamics of the 1-bromo-2,6-difluorobenzene molecule has been visualized via imaging the recoiling velocity distributions of photofragments. The measured recoiling angular distributions of the Br(2P3/2) product vary significantly with the increasing photon energy, arguing against the simple bond-fission mechanism within the C2v symmetry. Ab initio calculations reveal that in addition to the C-Br bond cleavage, two additional internal molecular coordinates that break the molecular symmetry are likely involved. The Br out-of-plane bending opens a direct dissociation pathway on the S1-1A″ (S1-1ππ*) state, while the asymmetric C-F stretching significantly changes the orientation of the transition dipole moment. The present study sheds new light on the effect of symmetry breaking in the photodissociation dynamics of symmetric aryl halides, highlighting the multi-dimensional feature of excited state potential energy surfaces.

Vibrationally resolved photoemissions of N2 (C3Πu → B3Πg) and CO (b3Σ+ → a3Π) by low-energy electron impacts.

Vibrationally resolved photoemission spectra of the electronic-state transitions C3Πu → B3Πg of N2 and b3Σ+ → a3Π of CO following low-energy electron impacts are measured with a crossed-beam experimental arrangement. The absolute cross sections of C3Πu (ν') → B3Πg (ν″) of N2 are presented for the vibrational state-to-state transitions (ν',ν″) = (0,0), (0,1), (1,0), (1,2), and (2,1). The excitation cross sections of the metastable state C3Πu of N2 show the maxima at the electron-impact energies 14.10 (ν' = 0) eV and 14.50 (ν' = 1) eV, which are potentially related to the core-excited vibrational Feshbach resonant state 2Σu + of N2 - formed by electron attachment. The absolute cross sections of b3Σ+ (ν' = 0) → a3Π (ν″ = 0, 1, 2, 3, 4) of CO are given by the calibrations with those of N2 measured in this work. Besides the maximum excitation cross section 5.85 × 10-18 cm2 at 10.74 eV of the CO b3Σ+ (ν' = 0) state, some fine structures on the excitation function profile are attributed to different shapes and Feshbach resonant states of CO- formed by electron attachment, while the others arise from the direct electron-impact excitation. Some discrepancies, particularly for N2, between the present data and the results available in the literature studies arise from different experimental techniques and data-processing procedures. Furthermore, contributions of physical processes such as wave-packet evolution and non-Franck-Condon dynamics are highlighted here.

Structural study of TTR-52 reveals the mechanism by which a bridging molecule mediates apoptotic cell engulfment.

During apoptosis, apoptotic cells are removed by professional phagocytes or neighboring engulfing cells either directly through phagocytic receptors or indirectly through bridging molecules that cross-link dying cells to phagocytes. However, how bridging molecules recognize "eat me" signals and phagocytic receptors to mediate engulfment remains unclear. Here, we report the structural and functional studies of Caenorhabditis elegans TTR-52, a recently identified bridging molecule that cross-links surface-exposed phosphatidylserine (PtdSer) on apoptotic cells to the CED-1 receptor on phagocytes. Crystal structure studies show that TTR-52 has an open ß-barrel-like structure with some similarities to the PKCα-C2 domain. TTR-52 is proposed to bind PtdSer via an "ion-mediating" PtdSer-binding mode. Intensive functional studies show that CED-1 binds TTR-52 through its N-terminal EMI domain and that the hydrophobic region of the TTR-52 C terminus is involved in this interaction. In addition, unlike other PtdSer-binding domains, TTR-52 forms dimers, and its dimerization is important for its function in vivo. Our results reveal the first full-length structure of a bridging molecule and the mechanism underlying bridging molecule-mediated apoptotic cell recognition.

A2Πu and 14Σu- States of Br2+ Studied by [1+1] Two-Photon Dissociation Spectroscopy in a Cold Ion Beam.

The A2Πu-X2Πg and 14Σu--X2Πg electronic transition spectra of Br2+ have been studied in the 500-720 nm wavelength range in a cold ion beam using a cryogenic cylindrical ion trap velocity map imaging spectrometer. The cryogenic ion trap produces a rotationally and vibrationally cold mass selected ion beam of Br2+, which simplifies the experimental spectra from vibrational hot bands and bands of mixed isotopic species. Vibrationally resolved photofragment excitation spectra are recorded for individual isotopologues of Br2+ (79Br2+, 79Br81Br+, 81Br2+) by [1+1] two-photon dissociation spectroscopy. Velocity map imaging of the photofragmented Br+ ions provides complementary information in the determination of spin-orbit states involved in corresponding electronic transitions. An experimental identification of the 14Σu- state has becomes possible based on the present experimental results and previously reported theoretical calculations. Vibrational analyses of the photofragment excitation spectra have yielded spectroscopic parameters, including state origins, harmonic frequencies, and anharmonic constants, for both A2Πu and 14Σu- states. The observed A2Πu state spin-orbit splitting and the "spin-forbidden" 14Σu--X2Πg transition band intensities indicate considerable spin-orbit couplings between the 14Σu- and A2Πu states. In addition, two groups of weak vibrational bands are also observed in the experimental spectra of 79Br81Br+, which may be due to symmetry-forbidden transitions from the X2Πg ground state to low-lying gerade states.

N-loss photodissociation dynamics of N2O+(B2Π) near the NO+(Σ+1) + N(2P) dissociation limit.

Photodissociation dynamics of the N2O+ cation in its B2Π state has been experimentally studied in an energy region around the NO+(1Σ+) + N(2P) dissociation limit using a cryogenic cylindrical ion trap velocity map imaging spectrometer. The results show that the NO+(1Σ+) + N(2D) product channel dominates the dissociation dynamics and requires the NNO angle to change by 30°-50° prior to dissociation. The NO+(1Σ+) + N(2P) product channel, which directly correlates with the B2Π state but less competitive, opens immediately when the photon energy reaches the dissociation limits, indicating a flat dissociation pathway without bending on the B2Π state surface.

Foveated imaging for near-eye displays.

The angular resolution of current near-eye display devices is still far below human-eye acuity. How to achieve retina-level resolution while keeping wide field-of-view (FOV) remains a great challenge. In this work, we demonstrate a multi-resolution foveated display with two display panels and an optical combiner. The first display panel provides a wide FOV but relatively low resolution for the surrounding region, while the second one offers an ultra-high resolution for the central fovea region, by an optical minifying system which enhances the effective resolution by 5 ×. In addition, a switchable Pancharatnam-Berry phase deflector is employed to shift the high-resolution region. The proposed design effectively reduces the pixelation and screen-door effect in near-eye displays.