128 research outputs found

    Characteristics of broadband lightning emissions associated with terrestrial gamma ray flashes

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    To characterize lightning processes that produce terrestrial gamma ray flashes (TGFs), we have analyzed broadband (<1 Hz to 30 kHz) lightning magnetic fields for TGFs detected by the Reuven Ramaty High Energy Solar Spectroscopic Imager (RHESSI) satellite in 2004-2009. The majority (96%) of 56 TGF-associated lightning signals contain single or multiple VLF impulses superposed on a slow pulse that reflects a process raising considerable negative charge within 2-6 ms. Some TGF lightning emissions also contain VLF signals that precede any appreciable slow pulse and that we term precursor sferics. The analyses of 9 TGFs related to lightning discharges with location uncertainty <100 km consistently indicate that TGFs are temporally linked to the early portion of the slow process and associated VLF impulses, and not to precursor sferics. The nearly universal presence of a slow pulse suggests that the slow process plays an important role in gamma ray production. In all cases the slow process raises negative charge with a typical mean current moment of +30 kA km. The resulting charge moment change ranges from small values below +10 C km to a maximum of +200 C km, with an average of +64 C km. The current moment waveform extracted from TGF sferics with single or multiple VLF impulses also shows that the slow process initiates shortly before the major TGF-associated fast discharge. These features are generally consistent with the TGF-lightning sequence reported by Lu et al. (2010), suggesting that the majority of RHESSI TGFs are produced during the upward negative leader progression prevalent in normal polarity intracloud flashes

    catena-Poly[[(1,10-phenanthroline)lead(II)]bis­(μ-5-chloro-2-hy­droxy­benzoato)]

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    In the title polymer, [Pb(C7H4ClO3)2(C12H8N2)]n, the Pb(II) ion displays a distorted pseudo-octa­hedral coordination geometry. The metal center is coordinated by six O atoms from four 5-chloro­salicylate ligands and two N atoms from a chelating phenanthroline ligand. The polymeric structure is built up from bridging carboxyl­ate O atoms, forming chains along [100]. The crystal structure is stabilized by π–π inter­actions between the 1,10-phenanthroline and 5-chloro­salicylate ligands, the shortest centroid–centroid separation between neighbouring aromatic rings being 3.652 (1) Å

    Optical emissions associated with narrow bipolar events from thunderstorm clouds penetrating into the stratosphere

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    Narrow bipolar events (NBEs) are signatures in radio signals from thunderstorms observed by ground-based receivers. NBEs may occur at the onset of lightning, but the discharge process is not well understood. Here, we present spectral measurements by the Atmosphere‐Space Interactions Monitor (ASIM) on the International Space Station that are associated with nine negative and three positive NBEs observed by a ground‐based array of receivers. We found that both polarities NBEs are associated with emissions at 337 nm with weak or no detectable emissions at 777.4 nm, suggesting that NBEs are associated with streamer breakdown. The rise times of the emissions for negative NBEs are about 10 μs, consistent with source locations at cloud tops where photons undergo little scattering by cloud particles, and for positive NBEs are ~1 ms, consistent with locations deeper in the clouds. For negative NBEs, the emission strength is almost linearly correlated with the peak current of the associated NBEs. Our findings suggest that ground-based observations of radio signals provide a new means to measure the occurrences and strength of cloud-top discharges near the tropopause.publishedVersio

    Enhanced B7-H4 expression in gliomas with low PD-L1 expression identifies super-cold tumors.

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    BACKGROUND: Characterizing expression profiles of different immune checkpoint molecules are promising for personalized checkpoint inhibitory immunotherapy. Gliomas have been shown as potential targets for immune checkpoint inhibitors recently. Our study was performed to determine coexpression levels of two major B7 immune regulatory molecules programmed death ligand 1 (PD-L1) and B7-H4, both of which have been demonstrated to inhibit antitumor host immunity in gliomas. METHODS: We assessed tumor tissues from stage II-IV primary gliomas (n=505) by immunohistochemistry (IHC) for protein levels of both PD-L1 and B7-H4. Gene coexpression analysis assessing clusters based on extent of PD-L1/B7-H4 classifier genes expression were investigated in two transcriptome datasets (The Cancer Genome Atlas and Chinese Glioma Genome Atlas). In addition, levels of immune cell infiltrates were estimated with IHC and RNA-seq data for assessing the tumor immune microenvironment of PD-L1/B7-H4 subgroups. RESULTS: High expression of PD-L1 and B7-H4 in gliomas was 23% and 20%, respectively, whereas coexpression of two proteins at high levels was limited to 2% of the cases. Comparable results were seen in RNA-seq datasets where PD-L1 mRNA expression levels negatively correlated with that of B7-H4. Gene coexpression modules clustered within each grade of gliomas demonstrated lack of double-high modules (cluster with high expression of both PD-L1 and B7-H4 classifier genes). B7-H4 mRNA expression levels showed negative correlation with extent of immune cell infiltration and High-B7-H4 module gliomas (high B7-H4 but low PD-L1 classifier genes expression) had less tumor-infiltrating lymphocytes (TILs) and tumor-associated macrophages (TAMs). IHC assessment also showed few TILs and TAMs in High-B7-H4 subgroup gliomas. CONCLUSIONS: The majority of gliomas express PD-L1 or B7-H4, however, coexpression of both at high levels is minimal. The high-B7-H4 patients could be considered as \u27super-cold\u27 gliomas with significantly deficient in TILs, suggesting that B7-H4 might inhibit T-cell trafficking into the central nervous system. This study demonstrated that PD-L1 and B7-H4 may serve as mutually compensatory immune checkpoint molecules in gliomas for immune targeted or active-specific immunotherapy. The distinct B7-H4 pathways modulating T-cell function and immune evasion in glioma patients deserved to be further explored in the future during immunotherapy
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