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Some of the most vexing problems of deep level relationship that remain in angiosperms involve the superrosids. The superrosid clade contains a quarter of all angiosperm species, with 18 orders in three subclades (Vitales, Saxifragales and core rosids) exhibiting remarkable morphological and ecological diversity. To help resolve deep-level relationships, we constructed a high-quality chromosome-level genome assembly for Tiarella polyphylla (Saxifragaceae) thus providing broader genomic representation of Saxifragales. Whole genome microsynteny analysis of superrosids showed that Saxifragales shared more synteny clusters with core rosids than Vitales, further supporting Saxifragales as more closely related with core rosids. To resolve the ordinal phylogeny of superrosids, we screened 122 single copy nuclear genes from genomes of 36 species, representing all 18 superrosid orders. Vitales were recovered as sister to all other superrosids (Saxifragales + core rosids). Our data suggest dramatic differences in relationships compared to earlier studies within core rosids. Fabids should be restricted to the nitrogen-fixing clade, while Picramniales, the Celastrales-Malpighiales (CM) clade, Huerteales, Oxalidales, Sapindales, Malvales and Brassicales formed an “expanded” malvid clade. The Celastrales-Oxalidales-Malpighiales (COM) clade (sensu APG IV) was not monophyletic. Crossosomatales, Geraniales, Myrtales and Zygophyllales did not belong to either of our well-supported malvids or fabids. There is strong discordance between nuclear and plastid phylogenetic hypotheses for superrosid relationships; we show that this is best explained by a combination of incomplete lineage sorting and ancient reticulation.

Anxiety is a common disease in the modern society which significantly affects people’s daily lives and function, thus it has become an increasingly highlighted issue. Anxiety is regulated by neural circuits in the brain. Therefore, the basal mechanism of anxiety has been studied, especially research based on the related neural circuits. For a long time, due to the limitations of science and technology, there was no breakthrough in research regarding anxiety. However, in recent years, due to the progress of technology, the research on anxiety neural circuits has made great progress. For example, the interaction among various brain regions, such as the central nucleus of the amygdala (CeA), the ventral tegmental area (VTA), the ventral hippocampus (vHPC), and so on. This article focuses on three brain regions: including BLA, BNST, and VTA, and illustrate their different roles and mechanisms in regulating anxiety. On this basis, this intensive study of anxiety will further promote the progress of anxiety research and provide therapeutic targets for the related treatment.

The development of blue emissive cationic Ir(III) complexes with no fluorine substitutions but with sufficient blue color purity and high phosphorescence efficiency has remained challenging. Here, fluorine-free cyan to deep blue emissive cationic Ir(III) complexes with phenylimidazole-type cyclometalated ligands (C∧N) are reported, which are [Ir(dphim)2(dmapzpy)]PF6 (1), [Ir(ipr-dphim)2(dmapzpy)]PF6 (2), [Ir(ipr-dphim)2(bipz)]PF6 (3), and [Ir(ipr-dphim)2(bicb)]PF6 (4). 1,2-Diphenyl-1H-imidazole (dphim) and 1-(2,6-diisopropylphenyl)-2-phenyl-1H-imidazole (ipr-dphim) are the phenylimidazole-type C∧N ligands, and 4-dimethylamino-2-(1H-pyrazol-1-yl)pyridine (dmapzpy), di(1H-pyrazol-1-yl)methane (bipz), and 3,3'-methylenebis(1-methyl-1H-imidazol-3-ium-2-ide) (bicb) are the neutral ancillary ligands (A∧A). In both solution and diluted films, complex 1 shows a cyan emission with the emission maxima at ∼472 and 495 nm, and complexes 2-4 provide a deep blue emission with the emission maxima at ∼460 and 480 nm. While the complexes exhibit low to moderate phosphorescence efficiencies (0.05-0.35) in a degassed CH3CN solution, they exhibit high phosphorescence efficiencies (up to 0.82) in diluted films. Theoretical calculations revealed that the mixed 3π-π* (C∧N-centered)/3MLCT (Ir → C∧N) states are responsible for the emission afforded by complexes 1-4, which undergo nonradiative deactivations induced by different types of metal-centered states. Organic light-emitting diodes with complexes 1-4 as phosphorescent dopants are fabricated by a solution process, which affords a blue-green to blue emission with the emission maxima at ∼460 and 490 nm for the blue devices and a high current efficiency at 28.1 cd A-1 for the blue-green device. Solid-state light-emitting electrochemical cells are also fabricated with complexes 1-2 as phosphorescent dopants, which provide green-blue to blue emission with a high luminance (up to 840 cd m-2) and current-efficiency (up to 16.8 cd A-1) under a constant-current driving. The work reveals that, by using phenylimidazole-type C∧N ligands and optimized A∧A ligands, blue emissive cationic Ir(III) complexes with no fluorine substitutions but with sufficient blue-color purity and a high phosphorescence efficiency can be developed.

Green to blue-green-emitting cationic iridium complexes free of sp2 C–F bonds, namely [Ir(CF3-dPhTAZ)2(bpy)]PF6 (1), [Ir(CF3-dPhTAZ)2(dmebpy)]PF6 (2) and [Ir(CF3-dPhTAZ)2(phpyim)]PF6 (3), have been designed and synthesized with 3,4-diphenyl-5-(trifluoromethyl)-4H-1,2,4-triazole (CF3-dPhTAZ) as the cyclometalating ligand (C^N) and 2,2′-bipyridine (bpy), 4,4′-dimethyl-2,2′-bipyridine (dmebpy) or 2-(1-phenyl-1H-imidazol-2-yl)pyridine (phpyim) as the ancillary ligand (N^N). In CH3CN solution, complexes 1–3 afford green to blue-green emission centered at 521, 508 and 498 nm, respectively. The electron-withdrawing CF3 group attached at the triazole ring in CF3-dPhTAZ largely blue-shifts (by over 20 nm) the emission of the complex through stabilizing the highest occupied molecular orbital. In doped films, the complexes afford sky-blue emission with near-unity phosphorescent efficiencies. In neat films, the complexes show largely suppressed phosphorescence concentration-quenching, with phosphorescent efficiencies of up to 0.66. Theoretical calculations reveal that the emission of the complexes can arise from either charge-transfer (Ir → C^N/C^N → N^N) or C^N/N^N-centered 3π–π* states, depending on the local environment of the complexes. Solid-state light-emitting electrochemical cells (LECs) based on the complexes afford green to blue-green electroluminescence centered at 525, 517 and 509 nm, respectively, with high current efficiencies of up to 35.1 cd A−1. The work reveals that CF3-dPhTAZ is a promising C^N ligand free of sp2 C–F bonds for constructing efficient cationic iridium complexes with blue-shifted emission.

Cationic iridium complexes that show blue-shifted emission and high phosphorescent efficiency have been pursued for their optoelectronic applications. Five cationic iridium complexes with 3,4,5-triphenyl-4H-1,2,4-triazole (tPhTAZ) type cyclometalating ligands (C^N) and 2,2'-bipyridine or 2-(pyridin-2-yl)-1H-benzo[d]imidazole type ancillary ligands (N^N) have been designed and synthesized. Their structures have been confirmed by X-ray crystallography, and their photophysical and electrochemical properties have been comprehensively characterized. In solution and thin films, the complexes afford efficient yellow to blue-green emission. The highest occupied molecular orbitals (HOMOs) of these complexes are delocalized over the C^N ligand and the iridium ion, and compared with the conventional 2-phenylpyridine (Hppy) ligand, the tPhTAZ ligand largely shifts the emission of the complex toward blue by over 40 nm through stabilizing the HOMO. Moreover, the peripheral phenyl rings in tPhTAZ provide steric hindrance to the complexes, which suppresses phosphorescence concentration-quenching of the complexes, leading to high luminescent efficiencies in neat films. Theoretical calculations have shown that the emission of the complexes originates from either the charge-transfer state (Ir/C^N → N^N) or the C^N/N^N-centered 3π-π* state, depending on the local surrounding of the complex. The complexes exhibit good electrochemical stability with reversible oxidation and reduction processes in solution. Solid-state light emitting electrochemical cells (LECs) using the complexes afford yellow to blue-green emission, with peak current efficiencies of up to 34.7 cd A-1 and maximum brightness of up to 256 cd m-2 at 3.0 V, which are among the highest for LECs based on cationic iridium complexes reported so far, indicating the great potential for the use of tPhTAZ-type C^N ligands in construction of cationic iridium complexes for LEC applications.

To determine the genetic structure ofA total of 271 erythromycin-resistant MRSA isolates were isolated from Sir Run Run Shaw Hospital (SRRSH) from 2013 to 2015. Whole-genome sequencing was performed for theA total of 64 isolates (64/271, 23.6%) wereMultiple copies of

Cave-dwelling ground beetles in China represent the most impressive specific diversity and morphological adaptations of the cavernicolous ground beetles in the world, but they have not been systematically examined in quantitative terms. The present study focuses on the application of geometric morphological methods to address the morphological adaptations of the tribe Trechini, the most representative group in China. We have employed a geometric morphometry analysis of the head, pronotum, and elytra of 53 genera of Trechini, including 132 hypogean and 8 epigean species. Our results showed that the overall morphological variation of cave carabids has gradually specialized from an anophthalmic to semi-aphaenopsian to aphaenopsian type. There were extremely significant differences (p &lt, 0.01) among four different adaptive types including aphaenopsian, semi-aphaenopsian, anophthalmic, and surface-dwelling Trechini when their adaptability to a cave environment was used as the basis for grouping. Furthermore, there were differences in the phenotypic tree of the head, pronotum, and elytra, and an integrated morphology. To the best of our knowledge, this is the first report on the analysis of the head, pronotum, and elytra of four different adaptive types of ground beetles in order to clarify the morphological adaptations of cavernicolous carabids to the cave environment.

Purpose: We investigated ocular accommodative responses and pupil diameters under different light intensities in order to explore whether changes in light intensity aid effective accommodation function training. Methods:A total of 29 emmetropic and myopic subjects (age range: 12–18 years) viewed a target in dynamic ambient light (luminance: 5, 100, 200, 500, 1000, 2000 and 3000 lux) and static ambient light (luminance: 1000 lux) at a 40 cm distance with refractive correction. Accommodation and pupil diameter were recorded using an open-field infrared autorefractor and an ultrasound biological microscope, respectively. Results: The changes in the amplitude of accommodative response and pupil diameter under dynamic lighting were 1.01 ± 0.53 D and 2.80 ± 0.75 mm, respectively, whereas in static lighting, those values were 0.43 ± 0.24 D and 0.77 ± 0.27 mm, respectively. The amplitude of accommodation and pupil diameter change in dynamic lighting (t = 6.097, p < 0.001) was significantly larger than that under static lighting (t = 16.115, p < 0.001).The effects of light level on both accommodation and pupil diameter were significant (p < 0.001). Conclusion: Accommodation was positively correlated with light intensity. The difference was about 1.0 D in the range of 0–3000 lux, which may lay the foundation for accommodative training through light intervention.

Cationic iridium complexes that show blue-shifted emission and high phosphorescent efficiency have been pursued for their optoelectronic applications. Five cationic iridium complexes with 3,4,5-triphenyl-4

A new subgenus, Huaius n. subgen. of the genus Pterostichus, is described to deal with the following three new species of ground beetles which were recently discovered from limestone caves in Centr...

A new genus and two new species of cavernicolous trechine beetles are reported from southern Guizhou Province, Southwest China: Miaotrechus mahua n. gen., n. sp. from the cave Miaoting, Getuhe cave system, Ziyun Miao & Buyi Zizhi Xian (Autonomous County), Anshun Shi; M. heweii n. sp. from the cave Jingua Dong, danzhai County, Qiandongnan Miao & Dong Zizhizhou (Autonomous Prefecture). Miaotrechus might be related to the genus Guizhaphaenops Vigna Taglianti, 1997, but it is an Anophthalmus-like, whereas Guizhaphaenops species are semi-aphaenopsian.

Deep insight into the nonradiative deactivation pathways in phosphorescent cationic iridium complexes is critically important for developing efficient blue-emitting complexes toward advanced applications. Here, we report the synthesis and photophysical and electrochemical characterizations of a blue-green-emitting cationic iridium complex [Ir(ppy)2(bipzpy)]PF6 (Hppy is 2-phenylpyridine, and bipzpy is 2,4-di(1H-pyrazol-1-yl)pyridine). The nonradiative deactivation pathways in [Ir(ppy)2(bipzpy)]PF6 have been elucidated through extensive density functional theory calculations. The calculations reveal that the higher-lying charge-transfer (CT) state in [Ir(ppy)2(bipzpy)]PF6, which arises from Ir/ppy → bipzpy transitions, favors nonradiative deactivation because of its large structural distortion compared to the ground state. Both the CT state and the dark metal-centered (3MC) state can be thermally accessed by the lowest-lying emitting triplet state at room temperature, with the former being much more easily ...

The diphenylvinyl motif with rotary phenyl rings has been widely used as a building block for the construction of luminescent materials with aggregation-induced emission (AIE) properties. Here, we report the use of 2,2-diphenylvinyl in an iridium complex and its influence on the luminescence properties of the complex. Surprisingly, the 2,2-diphenylvinyl motif attached to the cyclometalating ligand brings about no AIE; instead, it completely quenches the phosphorescence from the iridium complex in solution or films at room temperature or at 77 K. Hydrogenation of the vinyl group in 2,2-diphenylvinyl recovers the phosphorescence. Theoretical calculations reveal that in the lowest triplet state of the complex, the 2,2-diphenylvinyl motif undergoes a significant structural change; as a result, the spin-density in the lowest triplet state distributes almost exclusively on the triphenylethene moiety of the cyclometalating ligand, with little distribution on the iridium ion, leading to complete quenching of phosphorescence. This work reveals that introduction of conjugated molecular motifs with rotational groups (such as 2,2-diphenylvinyl) into iridium complexes should be carefully treated, because it could quench the phosphorescence rather than inducing AIE, which provides a guideline for the design of AIE phosphors based on transition metal complexes.

Qianaphaenops (Sanwangius) rowselli Tian et Chen, n. subgen., n. sp. is described from the Sanwang Dong-Erwang Dong cave system, northeastern Wulong, southern Chongqing, southwestern China. Sanwangius is markedly distinct by several important features from subgenera Qianaphaenops (s. str.) Uéno, 2000 and Tiankengius Tian et Huang, 2018. Larval characteristics of this new species are also provided. This is the first report of a Qianaphaenops species from Chongqing.

Sinaphaenops (s. str.) lipoin. sp. is described and illustrated from a limestone cave in central Guizhou Province, China. This new species is most similar to S. (s. str.) banshanicus Tian, Chen and Tang, 2017. Both species are members of a peculiar species-group in the nominate subgenus Sinaphaenops (s. str.) Ueno and Wang, 1991, based on the presence of anterior lateromarginal setae on the pronotum and preapical pores on the elytra. In addition, the male genital characteristics of S. (s. str.) orthogenysUeno, 2002 are described for the first time.

We unravel intriguing dynamical diradical behavior governed by structural fluctuation in pentacene using ab initio molecular dynamics simulation. In contrast to static equilibrium configuration of pentacene with a closed-shell ground state without diradical character, due to structural fluctuation, some of its dynamical snapshot configurations exhibit an open-shell broken-symmetry singlet ground state with diradical character, and such diradical character presents irregular pulsing behavior in time evolution. Not all structural changes can lead to diradical character, only those involving the shortening of cross-linking C-C bonds and variations of the C-C bonds in polyacetylene chains are the main contributors. This scenario about diradicalization is distinctly different from that in long acenes. The essence is that structural distortion cooperatively raises the HOMO and lowers the LUMO, efficiently reducing the HOMO-LUMO and singlet-triplet energy gaps, which facilitate the formation of a broken-symmetry open-shell singlet state. The irregular pulsing behavior originates from the mixing of normal vibrations in pentacene. This fascinating behavior suggests the potential application of pentacene as a suitable building block in the design of new electronic devices due to its magnetism-controllability through energy induction. This work provides new insight into inherent electronic property fluctuation in acenes.

Mental health education of the minority engineering college students still faces lots of problems. Those problems have prevented the further improvement of minority engineering students' personal qualities Thus, it is imperative to build mental health education model of the minority engineering college students.

A new method for fabricating sub-quarter micron X-ray mask patterns with high aspect ratio for HEMT and MOSFET is proposed. The key point of the method is to make the metal side-wall pattern with a supporter transparent to X-rays. Using the X-ray mask pattern made in the new method, a 93 nm line width positive resist pattern and a 260 nm line width negative resist pattern have been obtained. It is expected that this method could be applied to nanometer X-ray lithography for generation of the patterns of HEMT and MOSFET devices in the near future.