227,623 research outputs found
Guiodytes cavicola Tian 2013
Guiodytes cavicola Tian, 2013: 116 Type locality: Nongshui Cave, in Shangjia, Disu, Du’an County of northern Guangxi. Male genitalia (Figs. 2–3): Median lobe of aedeagus comparatively more elongate, moderately arcuate, ventral margin bisinuate, gradually contracted towards apex which is very narrow; basal orifice large; inner sac armed with a very long longitudinal copulatory piece; right paramere well developed, especially on base, left one narrower, shorter and very thin, each bearing 3–4 long setae apically. Additional material examined: 2 males and 1 female, Guangxi: Du’an County: Chengjiang: Ganwan: Nongzhong Cave I, 23 ° 56.644 N, 108 ° 10.072 E, 469 m, 2013 VI- 27, leg. Mingyi Tian, Wei Lin, Weixin Liu, Haomin Yin & Sunbin Huang; 1 male and 2 females, Guangxi: Du’an County: Longwan: Nongqu Cave I, 23 ° 56.021 N, 108 ° 10.962 E, 459 m, 2013 -VI- 27, leg. Mingyi Tian, Wei Lin, Weixin Liu, Haomin Yin & Sunbin Huang. All specimens are deposited in the insect collections of South China Agricultural University, Guangzhou, China (SCAU), except one male in Muséum National d'Histoire Naturelle, Paris, France (MNHN). Distribution: Du’an County, northern Guangxi. Known from three limestone caves in Disu, Chengjiang and Longwan, respectively (Fig. 1).Published as part of Tian, Mingyi, 2014, New records and a new species of the cavernicolous genus Guiodytes Tian, 2013 from Guangxi, China (Coleoptera: Carabidae: Scaritinae), pp. 355-362 in Zootaxa 3861 (4) on page 357, DOI: 10.11646/zootaxa.3861.4.5, http://zenodo.org/record/22532
Futaki Invariant and CM Polarization
This is an expository paper. We will discuss various formulations of Futaki invariant and its relation to the CM line bundle. We will discuss their connections to the K-energy. We will also include proof for certain known results which may not have been well presented or less accessible in the literature. We always assume that M is a compact Kahler manifold. By a polarization, we mean a positive line bundle L over M, then we call (M, L) a polarized manifold.EICPCI-S(ISTP)[email protected]
Morimotoidius zhushandong Pang & Tian
Morimotoidius zhushandong Pang & Tian Pang & Tian, 2014: 3 Additional material examined. 1 male, Zhuangxi Dong, Zhuangxi Cun, Hongtang Zhen, Yichun City, Jiangxi Province, China, 28 °00' 47.71 "N, 114 ° 19 ' 43.82 "E, 230 m in altitude, 22 -IX- 2014, leg. Sunbin Huang & Xinhui Wang, in SCAU. Distribution. China (Jiangxi). Known from two limestone caves in the bordering areas between Yichun City and Wanzai County, about 7 km apart from each other (Fig. 11).Published as part of Wang, Xinhui, Pang, Jianmei & Tian, Mingyi, 2015, Second highly modified hypogean species of the genus Morimotoidius Habu from western Jiangxi Province, China, with a new locality for M. zhushandong (Coleoptera: Carabidae: Platynini), pp. 587-593 in Zootaxa 4034 (3) on page 594, DOI: 10.11646/zootaxa.4034.3.10, http://zenodo.org/record/23362
Hexachaetus lateralis subsp. maindroni Tian et Deuve 2006, n. stat.
Hexachaetus lateralis maindroni Tian et Deuve, 2006, n. stat. (Figures 2–4) Hexachaetus maindroni Tian & Deuve, 2006: 149 Length: 19.0 mm; width: 8.0 mm. Habitus as in Fig. 2. Diagnosis. Large sized, polish, glabrous and shiny species; head, pronotum, side margin of elytra, whole apical margin of abdominal ventrite VII, tibiae and tarsi of legs dark brown, underside, femora and coxae yellowish brown; elytral marking narrow, not anchoreaform; labial palpomere 3 glabrous, slightly shorter than palpomere 2; labial palpomere 2 bisetose on inner margin, and with two more shorter setae near apex; maxillary palpomere 3 longer than 4; the median lobe of aedeagus stout, dramatically constricted at apex in profile; lamella broadly and extraordinary dilated in lateral aspect (Figs. 3–4). Remarks. Similar to H. lateralis lateralis not only on appearance, but also on genital structure. However, it is slightly larger than H. lateralis, elytra marking narrower at middle, extending only to intervals 2 (to intervals 3 in H. lateralis), and inner apical angle of elytra blunter than in H. lateralis lateralis. Material. 1 male, the holotype, “ Borneo, Sarawak, Kuching ”, “ 16 Oct. 1894 ”, “ Hexachaetus maindroni n. sp. det. Tian & Deuve, 2004 ”, “ Hexachaetus laeviceps M.”(det. Maindron M.), “ Museum Paris ”, and “ Ex Coll. M. Maindron”, in MNHN. Distribution. Malaysia (Fig. 20 b).Published as part of Tian, Mingyi & Deuve, Thierry, 2016, Re-definition and review of the Oriental genus Hexachaetus Chaudoir, 1871 (Coleoptera: Carabidae: Orthogoniini), pp. 540-554 in Zootaxa 4169 (3) on page 543, DOI: 10.11646/zootaxa.4169.3.7, http://zenodo.org/record/25802
Pestalotiopsis abietis C. M. Tian & M. Gu 2021, sp. nov.
<i>Pestalotiopsis abietis</i> C.M. Tian & M. Gu, <i>sp. nov.</i> Figure 2 <p> <b>MycoBank no:</b> MB 832473.</p> <p> <i>Etymology</i>:— <i>abietis</i>, named after the host <i>Abies fargesii</i></p> <p> <b>Asexual morph</b>: <i>Conidiomata</i> pycnidial in culture on PDA, globose, scattered or gregarious and confluent, semi-immersed, dark brown, 100–650 μm diam. <i>Conidiophores</i> often reduced to conidiogenous cells. <i>Conidiogenous cells</i> discrete ampulliform to lageniform, smooth, thin-walled, hyaline, with 1–2 proliferations, sometimes remain vegetative. <i>Conidia</i> 19.9–31.2 × 5.8–8.0 μm (<i>x</i> = 24.0 × 6.8 μm), fusiform, straight to slightly curved, 4–septate, basal cell conic to obconic, hyaline or slightly olivaceous, thin and verruculose, 2.4–8 μm long (<i>x</i> = 4.7 μm), with three median cells, doliform, concolourous, olivaceous, septa and periclinal walls darker than the rest of the cell, together 11.4–17.6 μm long (<i>x</i> = 14.8 μm) second cell from base 3.5–6.4 μm (<i>x</i> = 5 μm); third cell 3.8–6.1 μm (<i>x</i> = 4.9 μm); fourth cell 4– 5.8 μm (<i>x</i> = 4.9 μm); apical cell hyaline, conic, 2.4–6 μm long (<i>x</i> = 4.3 μm); with 1–3 tubular apical appendages (mainly 3), arising from the apex of the apical cell, 7.6–20.6 μm long (<i>x</i> = 14.1 μm); basal appendage 1.3–5.2 μm long.</p> <p>......continued on the next page</p> <p>......continued on the next page</p> <p>......continued on the next page</p> <p>The ex-type strains are marked with *, and NA means not available.</p> <p> <i>Culture characteristics:</i> —Colonies on PDA attaining 25–45 mm diam after 7 d at 25 °C, with smooth edge, whitish, with sparse aerial mycelium on the surface with black, gregarious conidiomata; reverse similar in color.</p> <p> <i>Materials examined:</i> — CHINA, Shaanxi Prov., Ningshan County, Qinling Mountain, Huoditang forest park, 33°26’7”N 108°26’48”E, 1570 m a.s.l., on needles of <i>Abies fargesii</i>, N. Jiang & C.M. Tian, 3 July 2018 (Holotype BJFC-S1584, ex-type CFCC 53011; <i>ibid.</i> living culture CFCC 53012 and CFCC 53013).</p> <p> <i>Notes:</i> —This new species is introduced as molecular data showed it to be distinct, which is also supported by morphological traits. In the phylogram, <i>P. abietis</i> appears most closely related to <i>P. parva</i>. However, <i>P. parva</i> has shorter conidia compared with <i>P. abietis</i> (16.5–20 μm in <i>P. parva</i> vs. 19.9–31.2 μm in <i>P. abietis</i>) (Maharachchikumbura <i>et al.</i> 2014b). Therefore, we confirmed that <i>P. abietis</i> could be described as a new taxon.</p>Published as part of <i>Gu, Mo, Hu, Dong-Wei, Han, Bing, Jiang, Ning & Tian, Cheng-Ming, 2021, Pestalotiopsis abietis sp. nov. from Abies fargesii in China, pp. 93-105 in Phytotaxa 509 (1)</i> on pages 96-101, DOI: 10.11646/phytotaxa.509.1.4, <a href="http://zenodo.org/record/5426012">http://zenodo.org/record/5426012</a>
Le Tian-Shan et les Kara-Kirghises
Nœlting F.-A.-M. Le Tian-Shan et les Kara-Kirghises. In: Le Globe. Revue genevoise de géographie, tome 83, 1944. p. 19
Energy-Efficient Train Operation: Conclusions and Future Work
This chapter gives the basic conclusions about energy-efficient train operation covering energy-efficient train driving, energy-efficient train timetabling, regenerative braking, energy storage systems and power supply networks. Future work that will develop energy-efficient train operation further include the interaction of connected driver advisory systems (C-DAS) and automatic train operation (ATO) with railway traffic management systems, cooperative train control in platoons of virtually coupled trains, digital twin technology and particularly its application to power supply systems, and the interaction between the railway network with the electrical power grid and renewable energy generation.Green Open Access added to TU Delft Institutional Repository ‘You share, we take care!’ – Taverne project https://www.openaccess.nl/en/you-share-we-take-care Otherwise as indicated in the copyright section: the publisher is the copyright holder of this work and the author uses the Dutch legislation to make this work public.Transport and Plannin
Actenoncus punctatus Tian and Deuve
Actenoncus punctatus Tian and Deuve (Figs. 3, 6 and 9) Actenoncus punctatus Tian and Deuve, 2006 b: 152 Diagnosis. Rather small, light dark brown, right mandible without median tooth, labrum emarginated at frontal margin, head and pronotum coarsely punctate, elytral striae shallow, punctures large and isolated; abdominal ventrite VII deeply emarginated at apical margin in male, aedeagus more slender. Length: 13.5 mm; width: 5.5 mm. Body light dark brown. Habitus as in Fig. 3. Surface very shiny, head and pronotum with sparse and small punctures, elytra glabrous. Microsculptural meshes densely isodiametric. Head as long as wide; eyes large, extraordinary prominent, neck constricted, labrum slightly emarginated at frontal margin, frontal impressions deep and short, not extending the level of fore margins of eyes; clypeus bisetose, base slightly raised; mandibles strong, right mandible without median tooth; palpi similar to those of above species; ligula narrow, bisetose at apex; mentum without median tooth, asetose, submentum with a pair of setae; palpiger unisetose; antennae similar to those of A. wallacei, but extending to basal one-fourth of elytra. Pronotum similar to that of above species (PW/PL= 1.6), but lateral expanded margins wider, basal margin slightly produced backwards in median portion. Elytra elongate ovate, EL/EW= 1.5, convex; base unbordered, widest a little behind middle, paralleled at sides; apex broadly truncate, inner angle nearly rectangular, pointed; elytral striae shallow, strial punctures large, well-marked and isolated; intervals flat, equal in width at middle, without puncture and setiferous pore, except a row of tiny punctures at basal part of interval 8. Prosternal process unbordered at apex. Hind tarsomere 4 slightly emarginated at apex. Abdominal ventrite VII slightly emarginated at apical margin in male (Fig. 6). Male genitalia. The median lobe of aedeagus slender and elongate, slightly expanded in median portion, the apical lamella slightly longer than wide, rounded at apex (Fig. 9). Female. Unknown. Distribution. Indonesia and Malaysia, occurring in the islands of Borneo and Sumatra. Materials examined. 1 male, the holotype, “Borneo Occ. Pontainak, 1899 ”, from west Borneo, Indonesia (MNHN); 1 male, a paratype, “Borneo, 3412 ”, “Bowring, 63.47 ” and “ Actenoncus sp. n. ”(NHML); 1 male, a paratype, “Sumatra, 1979, E. W. Diehl”, “Sinder Raya, 14. X., 40 km, W. Dolok M.”, in (NHMB); 1 male, “ Malaysia: Sabah Mt., Kinabalu Park, Poring Hot, Springs, 15–30. 12. 1995 ”, and “Coll. Natur. Museum Stuttgart, W. Schawaller” (NHMS).Published as part of Tian, Ming-Yi & Deuve, Thierry, 2009, A review of the genus Actenoncus Chaudoir (Coleoptera: Caraboidea: Orthogoniini), pp. 57-64 in Zootaxa 2135 on pages 62-63, DOI: 10.5281/zenodo.18848
Plectrocnemia bifurcata Tian 1993
Plectrocnemia bifurcata Tian 1993 (in Tian et al. 1993) (Figs 14A–14C) Material: 2 ♂, Kachin, road to Mt. Inwa Bum, 2240 m, 25.v.2006, leg. S. Naumann (pinned); 1 ♂, Kachin, road Pan Wah – Phemaw, 2260 m, 29–30.ix.2010, genitalia in glycerin vial, leg. S. Naumann (pinned) Remarks. The species was described from the Hengduan Mountains of Yunnan by Tian et al. (1993). At about the same year, it was named again as P. kainam Malicky 1993 from Myanmar, Kambaiti. The synonymy was already suspected by Malicky (2013), and it is herewith confirmed. The male genitalia are depicted in Figs 14A–14C in order to facilitate its future identification.Published as part of Mey, Wolfram & Malicky, Hans, 2021, Caddisflies from Myanmar: New records and descriptions of new species (Insecta, Trichoptera), pp. 533-565 in Zootaxa 5060 (4) on page 555, DOI: 10.11646/zootaxa.5060.4.4, http://zenodo.org/record/563798
- …
