137,405 research outputs found
Dreamy Eyes, Dreamy Eyes, what a wealth of hidden treasure [first line of chorus]
No full textstrophic with choruspiano and voiceads on inside front and on back covers for Jerome H. Remick & Co. stockJohns Hopkins University, Levy Sheet Music Collection, Box
146, Item 028Lyrics by Ren Shields. Music by George Evans.George Evans in The Runaways. Direction of F. Ray Comstock.unattrib. photo of George Evans; Starme
Dreamy Eyes, Dreamy Eyes, what a wealth of hidden treasure [first line of chorus]
No full textstrophic with choruspiano and voiceads on inside front and on back covers for Jerome H. Remick & Co. stockJohns Hopkins University, Levy Sheet Music Collection, Box
146, Item 028Lyrics by Ren Shields. Music by George Evans.George Evans in The Runaways. Direction of F. Ray Comstock.unattrib. photo of George Evans; Starme
ANALISIS MATERI DALAM APLIKASI DEUTSCH H?REN & LESEN SEBAGAI MEDIA PEMBELAJARAN BAHASA JERMAN KELAS X
Get PDFThis study uses a qualitative method with literature study which aims to describe the results of contentanalysis in the Deutsch H?ren & Lesen application as a means of learning German for class X. The data isextracted from the Deutsch H?ren & Lesen application based on Android games containing material A1to B2. with different themes in the form of questions and audio. The data used is A1 material with 14themes. However, the Deutsch H?ren & Lesen application needs to be adapted to the 2013 Curriculum tobe used as a learning reference according to the learning criteria in Indonesian media and education.Therefore, this article takes the formulation of the problem whether the German language material in theDeutsch H?ren & Lesen application is in accordance with the listening skills of class X semester 1. Thedata obtained is then analyzed, the analytical technique used is content analysis or content analysis usinglearning media theory, material suitability theory, audio teaching material theory and 2013 Curriculum.The results of the analysis explain in detail that the application of Deutsch H?ren & Lesen to the topics ofIch bin Tom, Struppi, Marie und Ihre Familie is very much in accordance with the 2013 Curriculum andhas a percentage score of 96% and media selection criteria has a percentage score of 91%
Platyscelis (Platyscelis) helanensis Bai & Ren 2019, sp. nov.
No full textPlatyscelis (Platyscelis) helanensis sp. nov. (Figs. 4, 25–26, 57–58) Diagnosis. This new species is similar to Platyscelis (Platyscelis) gebieni Schuster, 1915, but can be distinguished from the latter by the following characters: (1) punctures dense and fine on head (extremely dense and moderately coarse in P. gebieni); (2) pronotum with unconnected oval dense and fine punctures at sides (dense and coarse and merged partially in P. gebieni); (3) parameres narrow and long, dorsal side straight in lateral view (obviously wide, apex curved to dorsal side occasionally in P. gebieni). Description. Body black with weakly shining, tarsus, antennae and palpus weak brown. Male (Figs. 4, 25–26, 57). Anterior margin of frontoclypeus straight, surface with dense and fine punctures. Frons and genae weakly convex, with punctures dense and fine. Eyes transverse, with shallowly emarginate anterior margin. Antennae (Fig. 4: B) almost reaching base of pronotum, 2nd to 8th antennomeres cylindrical and thicker at apex, 9th to 10th almost spherical, and 11th sharped-oval. Length (width) ratio of 2nd to 11th antennal segments 29 (16): 76 (19): 41 (18): 40 (18): 38 (18): 39 (19): 39 (22): 33 (22): 33 (26): 43 (27). Pronotum (Fig. 4: A) transverse and convex, widest at base, 1.5 times as wide as long, 2.1 times as wide as head. Lateral margins nearly parallel from base to middle and arcuately narrowing toward apex. Ratio of width at anterior margin to basal 25: 49. Anterior margin nearly straight and posterior one straight. Anterior angles obtuse and posterior ones rectangular. Lateral margins edged in anterior margin and posterior one not edged, entire lateral margins edged, widely depressed from base to middle. Punctures fine and dense on disc, unconnected and oval at sides. Prothoracic hypomera with coarse wrinkles and sparse yellow setae. Prosternum before procoxae with yellow setae, prosternal process projecting beyond level of procoxae, weak sharp at apex in lateral view. Mesoventrite with punctures and yellow setae. Elytra oval and weak convex, base moderately wider than pronotum and widest at middle, 1.2 times as long as wide and 1.2 times as wide as pronotum. Surface rough, with shallowly dense and coarse punctures, while smaller and blurred at apex, and weak longitudinal carinae or traces. Lateral carina visible nearly completely in dorsal view and almost reaching sutural angle. Abdomen with short sparse yellow setae, not depressed at middle of 1st and 2nd ventrites. Profemora with sparse punctures and yellow setae. Protibiae (Fig. 4: D) gradually widened towards apex and curved at inner side, underside concave at apex and apical margin foliate extended, inner side with dense yellow hairbrush at apex. Protarsi (Fig. 4: C) strongly widened but narrower than apex of protibiae. Meso- and metafemora longer than profemora. Mesotibiae (Fig. 4: E) gradually widened toward apex with rufous strong setae. Mesotarsi (Fig. 4: F) moderately widened and narrower than apex of mesotibiae. Metatibiae (Fig. 4: G) straight, with rufous strong setae. Length (width) ratio of pro-, meso- and metafemora 27 (10): 30 (8): 38 (9), that of corresponding tibiae 25 (9): 26 (6): 34 (6), and protarsi 22 (28): 50 (71): 30 (63): 13 (33): 54 (23), mesotarsi 31 (35): 51 (57): 30 (41): 20 (29): 71 (24), metatarsi (Fig. 4: H) 109 (29): 57 (28): 39 (25): 82 (24). Aedeagus (Figs. 4: I–K, 25–26) 3.5 mm long and 0.9 mm wide. Parameres 1.0 mm long and 0.6 mm wide, narrow and long, widest at base and narrowing toward apex, outer margins with sharp hooks at apex, dorsal side straight in lateral view. Female (Fig. 58). Body wider, antennae not reaching base of pronotum, pro- and mesotarsi not widened, other characters similar to male. Measurements. Body length: ♂ 10.9–12.1 mm, ♀ 11.0– 11.6 mm and width: ♂ 5.7–6.3 mm, ♀ 5.9–6.5 mm. Type material. Holotype: ♂ (MHBU), CHINA: Inner Mongolia: Halawu, Helan Shan, 25–26.VII.2010, Guo-Dong Ren et al. leg . Paratypes: 27♂♂, 17♀♀ (MHBU), Guo-Dong Ren, Wen-Jun Hou, You-Zhi Yu & Long Jia leg., same data as holotype; 1♂ (MHBU), Helan Shan, 25.VI.1994; 11♂♂, 28♀♀ (MHBU), S of Halawu, Helan Shan, 21.VII.1990, Guo-Dong Ren leg.; 1♂ (MHBU), Halawu, Helan Shan, 23.VI.1994, Zhi-Qiang Sun & Chun-Yan Liu leg.; 1♀ (MHBU), W slope of Helan Shan, 24.VI.1994, Si-Qin Ge leg.; 2♂♂, 1♀ (MHBU), Beisi, Helan Shan, 24.VII.2010, Guo-Dong Ren, Wen-Jun Hou, You-Zhi Yu & Long Jia leg.; 1♂ (MHBU), Gulaben, Alxa Left Banner, 23.VII.2010, Guo-Dong Ren leg.; 2♂♂ (MHBU), Xiazigou, Alxa Left Banner, 6.VIII.2010, Guo-Dong Ren & Long Jia et al. leg.; Ningxia: 3♂♂, 2♀♀ (MHBU), Helan Shan, 1.VI.1987, Guo-Dong Ren leg.; 2♂♂, 2♀♀ (MHBU), Helan Shan, 2.VI.1987, Guo-Dong Ren leg.; 2♀♀ (MHBU), Helan Shan, 3.VI.1987, Guo-Dong Ren leg.; 1♂, 1♀ (MHBU), Helan Shan, 2.VII.1987, Guo-Dong Ren leg.; 1♀ (MHBU), Helan Shan, 1.VI.1988, Guo-Dong Ren leg.; 1♂ (MHBU), Helan Shan, 4.VI.1990, Guo-Dong Ren leg.; 2♂♂, 3♀♀ (MHBU), Helan Shan, 24.VI.1990, Guo-Dong Ren leg.; 1♀ (MHBU), Helan Shan, 4.V.1994, Guo-Dong Ren leg.; 1♀ (MHBU), Suyukou, Helan Shan, 20.VI.1990; 13♂♂, 31♀♀ (MHBU), Luo Shan, Tongxin, 1.VI.1984, Guo-Dong Ren leg.; 1♀ (MHBU), Luo Shan, Tongxin, 29.V.1989, Guo-Dong Ren leg.; 3♂♂, 7♀♀ (MHBU), Luo Shan, Tongxin, 20.VII.2009, Xin-Pu Wang & Hong-Fan Ran leg.; 1♂, 1♀ (MHBU), Yaoshan, Tongxin, 2100 m, 12.VIII.1987, Guo-Dong Ren leg.; 1♂ (MHBU), Yaoshan, Tongxin, 20.VIII.1987; 6♂♂, 4♀♀ (MHBU), Tongxin, 12.VIII.1987, Guo-Dong Ren leg.; 1♂ (MHBU), Tongxin, 12.VIII.1989, Guo-Dong Ren leg. Distribution. China: Inner Mongolia, Ningxia. Etymology. This species is named derived from the type locality—Helan Shan.Published as part of Bai, Xing-Long & Ren, Guo-Dong, 2019, Revision of the genus Platyscelis Latreille, 1818 from China (Coleoptera: Tenebrionidae: Platyscelidini), pp. 101-126 in Zootaxa 4609 (1) on pages 117-119, DOI: 10.11646/zootaxa.4609.1.4, http://zenodo.org/record/315080
Going Beyond Counting First Authors in Author Co-citation Analysis
Get PDFThe 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
The effect of NOM to TiO2: Interactions and photocatalytic behavior
No full textNatural organic matter (NOM) is ubiquitous in aquatic environment, which plays a predominant role in the sorption of pharmaceuticals onto the TiO2 nanoparticles. It is a matter of concern whether NOM could act as a surface sensitizer of TiO2 or not. In this context, the role of NOM is investigated for the photocatalytic degradation of carbamazepine (CBZ) using TiO2. Four different ratios of NOM:TiO2 were used varying from 400μgg-1 to 400mgg-1. The findings reveal that small amounts of NOM could enhance the TiO2 efficiency up to 8%. Electron paramagnetic spectroscopy (EPR), along with size exclusion chromatography with dissolved organic carbon detection (SEC-OCD) and nuclear magnetic resonance spectroscopy (NMR) reveal the occurring mechanism. TiO2 binds small molecular size fractions of NOM and breaks aromatic bonds of adsorbed NOM transforming it to stranded alkyl groups. This modified TiO2 bears a significant amount of electrons (e-) and lesser holes (h+) than the purified TiO2 and when irradiated, produces hydroxyl radicals which degrade CBZ
Asynchronous H∞ filtering for semi-Markov jump T-S fuzzy systems within partial state delay and deception attack: Applied to aircraft-pilot state estimation
No full textThis article addresses an asynchronous filter design problem within partial state delay and deception attack for a class of discrete-time semi-Markov jump Takagi-Sugeno (T-S) systems which can describe estimation process for human pilot cognitive property. First, the emission probability, which relates to system mode and filtering mode, is introduced to consider the system process with asynchronously observation scheme. Second, state delay-independent condition and state delay-dependent condition de-signed within state delay boundary are proposed under the H & INFIN; performance index & gamma;. Third, the system output signal under deception attack is adopted as the information interference during the transmitted filter process. Through the Lyapunov-Krasovskii approach, stability of the proposed filtering scheme that is mode dependent can be guaranteed. Moreover, the filtering mode is also dynamically changed ac-cording to the prescribed asynchronous formula. A numerical example considered for aircraft-pilot state estimation is used to demonstrate the effectiveness and applicability of our proposed filtering method by obtaining the minimum & gamma;. Experiments show that filter could play a better role in advancing signal estimation in aircraft-pilot state estimation scenario with properties like state delay and deception attack. Also, it contributes to modelling the fully human pilot cognitive decision-making in a human-computer interaction scenario
Similsciophila Shi & Shih & Ren 2014, gen. nov.
No full textSimilsciophila gen. nov. Type species: Similsciophila singularis sp. nov. Species included: Similsciophila singularis sp. nov. and Similsciophila sinuata sp. nov. Diagnosis Body medium-sized, covered with long and dense pubescence. Mesonotum convex. Scutellum sharp and clearly projecting. Forewing Sc elongate, shorter than one-half of wing length; sc-r situated distinctly basal to Rs origin, arising near midway between h to Sc ending at margin; cell r distinctly large, longer than one-sixth of wing length; Rs furcated distad to fork of M 1+2; bRs longer than r-m; R 1 slightly curved; both R 1 and R 4+5 divergent terminally; R 4+5 arched near its mid-length; stem of M not developed and thin; M 1+2 furcated slightly distad to level of Sc ending. Tibiae and tarsi with short sparse setae. Etymology The generic name is derived from the Latin (simil -), in reference to similar, and sciophila is from the generic name Mesosciophila. Remarks Based on the venation, Similsciophila gen. nov. is distinguished from Mesosciophilopsis Blagoderov, 1993 and Jurasciophila Li and Ren, 2009 by the following characters: wing longer and wider; cell r distinctly larger, and longer than one-sixth of wing length. The new genus is similar to the genus Paramesosciophilodes Zhang, 2007, but differs mainly by bRs longer than r-m. It also differs from Mesosciophilina Kovalev, 1985, Mesosciophilodes Rohdendorf, 1946 and Mesosciophila Rohdendorf, 1946 in that R 4+5 arched near its mid-length. Distribution China. Key to genera of mesosciophilid gnats 1. Cell r distinctly small, equal to or shorter than one-sixth of wing length.......... 2 - Cell r distinctly large, longer than one-sixth of wing length............................... 3 2. bRs equal to or shorter than r-m.................. Mesosciophilopsis Blagoderov, 1993 - bRs significantly longer than r-m........................ Jurasciophila Li and Ren, 2009 3. R 4+5 arched near its mid-length.......................................................................... 4 - R 4+5 slightly arched or almost linear near its mid-length................................... 5 4. bRs equal to or shorter than r-m................... Paramesosciophilodes Zhang, 2007 - bRs longer than r-m........................................................ Similsciophila gen. nov. 5. Cross-vein r-m converges with M 1+2 at obtuse angle......................................... 6 - Cross-vein r-m converges with M 1+2 at right angle....................................................................................................................... Mesosciophilina Kovalev, 1985 6. R 2+3 straight, almost perpendicular to R 4+5...... Mesosciophilodes Rohdendorf, 1946 - R 2+3 oblique, cross with R 4+5 at obtuse angle........ Mesosciophila Rohdendorf, 1946Published as part of Shi, GuiFeng, Shih, ChungKun & Ren, Dong, 2014, A new genus with two new species of mesosciophilids from the Middle Jurassic of China (Diptera: Nematocera: Mesosciophilidae), pp. 1147-1158 in Journal of Natural History 49 (19) on pages 1149-1150, DOI: 10.1080/00222933.2014.951085, http://zenodo.org/record/400590
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