1,723,476 research outputs found
Wen xuan: liu shi juan. v.1
梁昭明太子選 ; [李善注].綫裝, 1函.框20.4x13.6公分, 10行21字, 小字雙行, 白口, 雙黑魚尾, 四周單邊, 版心中鐫"文"及卷次, 下鐫葉次及刻工名.目錄末載"嘉靖元年十二月望日金臺汪諒古板校正新刊".封面有徐紹棨題"此為香山黃芑香先生舊藏", "明汪諒翻刻元本"With: 唐李崇賢上文選注表 / 李善.鈐有"香山黄氏鑒藏書畫記", "黄紹昌印", "屺鄉所藏", "足吾所好玩天老焉", "紹昌之印", "屺鄉", "信笈", "黎氏之子", "徐紹棨"等印.Xian zhuang, 1 han.Kuang 20.4 x 13.6 gong fen, 10 hang 21 zi, xiao zi shuang hang, bai kou, shuang hei yu wei, si zhou dan bian, ban xin zhong juan "Wen" ji juan ci, xia juan ye ci ji ke gong ming.Mu lu mo zai "Jiajing yuan nian shi er yue wang ri Jintai Wang Liang gu ban jiao zheng xin kan".Feng mian you Xu Shaoqi ti "Ci wei Xiang Shan Huang Qixiang xian sheng jiu cang", "Ming Wang Liang fan ke yuan ben"Liang Zhaoming tai zi xuan ; [Li Shan zhu].With: Tang Li Chongxian shang wen xuan zhu biao / Li Shan.Qian you "Xiang Shan Huang shi jian cang shu hua ji", "Huang Shaochang yin", "Qixiang suo cang", "Zu wu suo hao wan tian lao yan", "Shaochang zhi yin", "Qixiang", "Xin ji", "Li shi zhi zi", "Xu Shaoqi" deng yin
Chinese Listed Firms' Annual Reports (2008-2020)
We hand-collect Chinese listed firms’ annual reports between 2008 and 2020 from firms’ official websites. In addition, we also freely share Chinese listed firms’ annual reports' PDF and TXT files between 2008 and 2020 in the permanent download link(See: "https://pan.baidu.com/s/1CVXH-DTaAJ_5i1duDN96vA?pwd=8nh3")
Replication Data for: Time-frequency volatility spillovers between Chinese renminbi onshore and offshore markets during the COVID-19 crisis
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Taxonomic revision of Australasian diving beetles in the genus Leiodytes Guignot 1936 (Coleoptera: Dytiscidae, Bidessini)
Hendrich, Lars, Wang, Liang-Jong, Balke, Michael (2021): Taxonomic revision of Australasian diving beetles in the genus Leiodytes Guignot 1936 (Coleoptera: Dytiscidae, Bidessini). Zootaxa 4990 (1): 23-44, DOI: https://doi.org/10.11646/zootaxa.4990.1.
What axons tell each other: axon–axon signaling in nerve and circuit assembly
A remarkable feature of nervous system development is the ability of axons emerging from newly formed neurons to traverse, by cellular scale, colossal distances to appropriate targets. The earliest axons achieve this in an essentially axon-free environment, but the vast majority of axons eventually grow along a scaffold of nerve tracts created by earlier extending axons. Signal exchange between sequentially or simultaneously extending axons may well represent the predominant mode of axonal navigation, but proportionally few efforts have so far been directed at deciphering the underlying mechanisms. This review intends to provide a conceptual update on the cellular and molecular principles driving axon–axon interactions, with emphasis on those contributing to the fidelity of axonal navigation, sorting and connectivity during nerve and circuit assembly
Zema montana Wang & Liang, sp. nov.
Zema montana Wang & Liang, sp. nov. (Figs. 2, 12– 21) Description ɗ, length (from apex of vertex to tip of fore wings) 5.9–7.2 mm; fore wings length: 4.8–5.6 mm. General color brown; two patches on disc of vertex and a narrow, longitudinal stripe beyond median carina on pronotum blackish; frontal disc and clypeus largely fuscous; a broad band overlying fronto-clypeal suture ivory-white; clypeus with two, longitudinal piceous stripes beyond median carina; tip of rostrum fuscous; eyes reddish; most of gena ivory-white, with a blackish patch between eye and lateral margin of vertex and a large circular, black patch below eye; antennae with pedicel black, sensory plaque organs white; pronotum with ventral portion of lateral lobes covered with an oblique, blackish stripe, and the marginal portion ivory-white; mesonotum with irregular, blackish stripes, base of mesoscutellum with fuscous suffusion; legs covered with longitudinal, fuscous stripes on femora, tibiae, pro- and mesotarsi; abdominal sclerites blackish; fore wings transparent, veins brown, apex of clavus with blackish suffusion. Vertex (Fig. 12) distinctly shorter in midline line than breadth at base (2.14: 1). Frons (Fig. 13) longer in middle than the widest breadth (1.44: 1), with a broad callus at anterior margin, longitudinal carina, which between middle line and lateral carina, nearly parallel, uniting with median carina in the broad callus. Clypeus (Figs. 13, 14) with thicken median carina. Male genitalia (Figs. 17–21) relatively large, Periandrium (Figs. 17, 18, 20) large and elongate, symmetrical, with its basal half surrounding basal 1 / 2 of penis; penis slender and elongate, distinctly sinuate, apical half directed posteroventrally in lateral view, apex distinctly forked. Distribution Southwestern China (Yunnan). Remarks This species can be distinguished from Z. gressitti Fennah by the median carina of vertex percurrent (median carina only present in basal two-thirds in Z. gressitti), periandrium symmetrical (periandrium asymmetrical, denticulate on apical margin in Z. gressitti), and penis distinctly sinuate, much longer than that of Z. gressitti (about 4: 3), apex distinctly forked (penis appreciably sinuate, forming a distinctly fork from middle part in Z. gressitti).Published as part of Wang, Rong-Rong & Liang, Ai-Ping, 2007, Taxonomic study of the genus Zema Fennah (Hemiptera: Fulgoromorpha: Tropiduchidae) from China, pp. 61-68 in Zootaxa 1436 on pages 66-68, DOI: 10.5281/zenodo.17587
FIGURE 10 in Taxonomic revision of Australasian diving beetles in the genus Leiodytes Guignot 1936 (Coleoptera: Dytiscidae, Bidessini)
FIGURE 10. Maximum likelihood tree for Australasian Leiodytes. Neighbour joining tree (p-distances) calculated with Geneious (11.0.4.) software. The stars mark those specimens distributed over two divergent clades of L. migrator, which, however, occur syntopically.Published as part of Hendrich, Lars, Wang, Liang-Jong & Balke, Michael, 2021, Taxonomic revision of Australasian diving beetles in the genus Leiodytes Guignot 1936 (Coleoptera: Dytiscidae, Bidessini), pp. 23-44 in Zootaxa 4990 (1) on page 39, DOI: 10.11646/zootaxa.4990.1.2, http://zenodo.org/record/498275
Going Beyond Counting First Authors in Author Co-citation Analysis
The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation
counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings
are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that
only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into
account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
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