343,979 research outputs found
Acer sinopurpurascens W. C. Cheng
Acer sinopurpurascens W.C.Cheng in Chien & Cheng (1931: 62). Type:— CHINA. Zhejiang [Chekiang]: Western Tian Mu Shan [Tienmu-shan], elev. 1200–1300 m, 23 April 1931, W. C. Cheng 2424 (PE00023445, lectotype designated by Lin et al. 2009; isolectotypes A00245405, CQNM0015724, IBSC0002074, K000640863, NAS00071819, PE00023443, PE00023446, PE00023448). Remaining syntypes: CHINA. Zhejiang: Western Tianmushan, elev. ca. 845, 16 August 1929, S. S. Chien 845 (A00050488, CQNM0015723, NAS00071817, NAS00071818, NY00337718, PE00023444, K000640862); elev. 1200–1300 m, 23 April 1931, W. C. Cheng 2429 (A00245404, IBSC0002073, K000640864, LBG00076624, PE00023447). Note: —In the protologue, Chien & Cheng (1931) designated three gatherings as types of flowering, staminate and pistillate, respectively. Lin et al. (2009) chose a duplicate of staminate at PE (00023445) as the lectotype. The isolectotypes and remaining syntypes are listed above.Published as part of Chen, Feng & He, Hai, 2022, The historical relics in Chongqing Natural History Museum: An annotated checklist of original materials for 37 names of Chinese seed plants, pp. 38-52 in Phytotaxa 530 (1) on page 46, DOI: 10.11646/phytotaxa.530.1.3, http://zenodo.org/record/582393
Fagus chienii W. C. Cheng 1935
<p> <i>Fagus chienii</i> W.C.Cheng (1935: 70).</p> <p> Type:— CHINA. Sichuan [Szechuan]: W. Pingwu Xian [Pingwu hsien], elev. ca. 1300 m, 17 August 1931, <i>W. C. Cheng 2903</i> (lectotype designated here, NAS00070338; isolectotypes A00033870, CQNM0017387, E00098603, IBSC0001170, K000832761, MICH1109337, NAS00070339, NY00248568, PE00022177, PE00022178, PE00022179, PE00022180, PE00022181, PE00022182, PE00022180, SYS00054972, US 00409518).</p> <p> <b>Note</b>:—In the protologue, Cheng indicated <i>W.C. Cheng 2903</i> as the type, but he did not specify the herbarium where the type is deposited. In searching in various herbaria, 18 duplicates were traced and all of them are syntypes since no holotype was designated under Art. 9.6 (Turland <i>et al</i>. 2018). Most duplicates bear cupules and the identification annotation of W. C. Cheng and are well preserved. NAS00070338 is designated here as the lectotype for the reason Cheng used to work in NAS. In the protologue, Cheng (1935) stated the locality of the type at a place near “Yao-erpa” in West of Pingwu Xian; however, none of the duplicates with a label bearing this locality, and it is also uncertain whether “Pingwuhsien” means the present Pingwu Town. For efforts to trace this type locality has not been successful, the identity of this tree species is still uncertain (e.g. Huang <i>et al</i>. 1999).</p>Published as part of <i>Chen, Feng & He, Hai, 2022, The historical relics in Chongqing Natural History Museum: An annotated checklist of original materials for 37 names of Chinese seed plants, pp. 38-52 in Phytotaxa 530 (1)</i> on page 40, DOI: 10.11646/phytotaxa.530.1.3, <a href="http://zenodo.org/record/5823939">http://zenodo.org/record/5823939</a>
Cheng_et_al_supplemental – Supplemental material for Limitations of the Avp-IRES2-Cre (JAX #023530) and Vip-IRES-Cre (JAX #010908) Models for Chronobiological Investigations
Supplemental material, Cheng_et_al_supplemental for Limitations of the Avp-IRES2-Cre (JAX #023530) and Vip-IRES-Cre (JAX #010908) Models for Chronobiological Investigations by Arthur H. Cheng, Samuel W. Fung and Hai-Ying Mary Cheng in Journal of Biological Rhythms</p
Wetting transitions of liquid hydrogen films
Calculations are presented of the wetting properties of liquid hydrogen films on various substrates. The well depth D for the adsorption potential is even smaller for alkali metal substrates than for noble gas surfaces. A simple model calculation leads to the prediction that wetting transitions should then occur at a temperature T(w) about 20 K. Quartz microbalance data obtained for H-2 on Rb are consistent with this result. Specifically, T(w) is found to be 17.89 +/- 0.04 K. The wetting phase diagram is found to be in good agreement with thermodynamic expectations
Seasonal activity and reproduction of two syntopic white-toothed shrews (Crocidura attenuata and C. kurodai) from a subtropical montane forest in central Taiwan
Molecular engineering of copolymers with donor-acceptor structure for bulk heterojunction photovoltaic cells toward high photovoltaic performance
A series of donor-acceptor (D-A) conjugated copolymers with benzo[1,2-b:4,5-b-]dithiophene (BDT) as donor and two different electron-accepting groups bithiophenevinyl-2-pyran-4-ylidenemalononitrile (TVM) and benzothiadiazole (BT) moieties as acceptors is designed and synthesized. The optical and electrochemical properties show that the band gaps of the copolymers are in the range of 1.70-1.84 eV, and the HOMO and LUMO energy levels can be tuned effectively by controlling the varied ratios between TVM and BT because of the change of the ICT interaction between donor and acceptor, the electron delocalization degree, and the electron cloud density distribution of the copolymers. Bulk heterojunction photovoltaic devices are fabricated by using the copolymers as donors and (6,6)-phenyl-C61-butyric acid methyl ester (PC61BM) or (6,6)-phenyl-C71-butyric acid methyl ester (PC71BM) as acceptors. The optimized photovoltaic performances show that the open-circuit voltage (Voc) was gradually increased from 0.7 to 0.94 V when decreasing the HOMO energy levels of copolymers, and the short-circuit current density (Jsc) is greatly improved by increasing the absorption spectrum in the visible region, increasing the hole mobility and optimizing the morphologies of blend films between copolymers and PCBM. The optimized photovoltaic performance with a Voc of 0.78 V, J sc of 5.47 mA/cm2, fill factor (FF) of 0.40, and power conversion efficiency (PCE) of 1.67% under simulated AM 1.5 solar irradiation of 100 mW/cm2 is obtained by the copolymer PM50 (PM50:PC 61BM, 1:3 w/w, in CB solution). This is due to its high hole mobility and interpenetrating network morphology of PM50:PC61BM blend film. The photovoltaic device based on PM50:PC71BM shows a Jsc of 8.32 mA/cm2 and a PCE of 2.89%
Litsea auriculata S. S. Chien & W. C. Cheng 1931
Litsea auriculata S.S.Chien & W.C.Cheng (1931: 59). Type:— CHINA. Zhejiang [Chekiang]: Western Tian Mu Shan [W. Tien-mushan], elev. ca. 1100 m, 8 August 1929, S. S. Chien 601 (PE00028512, lectotype designated by Lin et al. 2016; isolectotypes A00041694, CQNM0015781, K000793089, NF2000700, NAS00070861, PE00028938, PE00434507). Remaining syntypes: CHINA. Zhejiang: Western Tian Mu Shan, elev. 800–1200 m, 17 April 1931, W. C. Cheng 2348 (A00041692, CQNM0015783, IBSC000227, K000793088, NF2000695, NY00355220, PE00028503, PE00028504, PE00028505, PE00028506) and W. C. Cheng 2349 (A00041693, CQNM0015784, IBSC0000229, K000793087, LBG00072037, NAS00070859, NAS00070860, NF2000694, NY00355221, PE00028508, PE00028509, PE00028510, PE00028511). Note:— In the protologue, Chien & Cheng (1931) designated S.S. Chien 601 (fruiting), W.C. Cheng 2348 (pistillate) and W.C. Cheng 2349 (staminate) deposited at the herbarium of Biological Laboratory of the Science Society of China as the type, and all of them are syntypes according to Art.9.6 (Turland et al. 2018). Lin et al. (2016) designated PE00028512 as the lectotype. The available isolectotypes and remaining syntypes are traced at the above listed herbaria.Published as part of Chen, Feng & He, Hai, 2022, The historical relics in Chongqing Natural History Museum: An annotated checklist of original materials for 37 names of Chinese seed plants, pp. 38-52 in Phytotaxa 530 (1) on page 42, DOI: 10.11646/phytotaxa.530.1.3, http://zenodo.org/record/582393
The Impacts of Lymph on the Adipogenesis of Adipose-Derived Stem Cells
Background: The pathophysiology of adipose proliferation or differentiation in extremity lymphedema has not been thoroughly studied. This study investigated the impacts of the lymph harvested from lymphedematous limbs on the adipogenesis of adipose-derived stem cells (ASCs). Methods: ASCs were isolated from the adipose tissue of normal extremities and cultured with lymph collected from Cheng lymphedema grade III to IV patients or adipogenic differentiation medium (ADM) and further subjected to differentiation and proliferation assay. The expression of adipogenesis genes was examined by real-time polymerase chain reaction to investigate the effect of lymph on ASCs. The level of adipogenic cytokines in the lymph was also evaluated. Results: The adipocytes were significantly larger in lymphedema fat tissue compared with that in normal fat tissues (P < 0.00). The adipogenesis of ASCs cultured in lymph was significantly enhanced compared with in ADM (P = 0.008) on day 10, suggesting that the adipogenesis of ASCs was promoted under the lymph-cultured environment. The expression of adipogenesis genes, peroxisome proliferator-activated receptor (P = 0.02), CAAT/enhancer-binding protein α (P = 0.008); fatty-acid binding protein (P = 0.004), and lipoprotein lipase (P = 0.003), was statistically elevated when the ASCs were cultured with lymph. The insulin content in lymph was statistically higher in lymph (P < 0.001) than in plasma. Conclusions: The adipogenesis of ASCs was promoted under the lymph-cultured environment with statistically increased adipogenesis genes of peroxisome proliferator-activated receptor, CAAT/enhancer-binding protein α, fatty-acid binding protein, and lipoprotein lipase. The excess lymph accumulated in the lymphedematous extremity contained a greater insulin/insulin-like growth factor-2. These adipogenic factors promoted the expression of early adipogenesis genes and led ASCs to undergo adipogenesis and differentiated into adipocytes. Clinical Relevance Statement: The accumulation of adipose tissue in the lymphedema region was contributed from the content of excess lymph
The application of Jing-Jia-Ji and Hua-Tuo-Jia-Ji in small animals. Proceeding of the 34 annual international congress on veterinary acupuncture.
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