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    Flatfronta Chen & Li

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    Key to species of Flatfronta Chen & Li 1. Male pygofer ventral process surpassing anterior margin of pygofer in ventral view (Viraktamath & Webb, 2019: Fig. 21 B).................................................................................................... 2 - Male pygofer ventral process not reaching anterior margin of pygofer (Ishihara, 1961: Fig. 96)....................... 3 2. Male pygofer ventral process forked distally (Chen, Li & Yang, 2008: Fig. 22) (China)................ F. pronga Chen & Li - Male pygofer ventral process not forked distally (Viraktamath & Webb, 2019: Figs. 21 A–B) (India)................................................................................................. F. bella Viraktamath & Webb 3. Forewing 4 th apical cell without brown marking (Ishihara, 1961: Fig. 93).......................... F. grandis (Ishihara) - Forewing 4 th apical cell with brown marking.................................................................4 4. Aedeagus short and stout, shorter than connective (Fig. 12); style apophysis with truncate apex (Figs. 4–5).................................................................................................... F. dibangi sp. nov. - Aedeagus elongate, broader at base and narrowed distally, about 3X as long as connective (Fig. 22); style apophysis finger-like with rounded apex (Fig. 16)................................................................. F. uttara sp. nov.Published as part of M. Meshram, Naresh & Nikoshe, Akash P., 2020, Two new species of bamboo-feeding leafhopper genus Flatfronta (Hemiptera Cicadellidae, Deltocephalinae) from India, pp. 176-180 in Zootaxa 4758 (1) on page 177, DOI: 10.11646/zootaxa.4758.1.8, http://zenodo.org/record/373091

    Flatfronta dibangi M.Meshram & Nikoshe 2020, sp. nov.

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    Flatfronta dibangi sp. nov. Figs 1-12. FIG. (1–12) Flatfronta dibangi sp. nov. 1–2. Habitus dorsal, lateral; 3. Face; 4–5. Style dorsal, apophysis magnified (ventral); 6–8. Pygofer lateral, ventral; 9. Subgenital plate with valve; 10-12. Aedeagus dorsal with Connective, magnified apical shaft, aedeagus lateral. Yellow, crown with one reddish orange longitudinal stripe on either side of median line reaching anterior margin of pronotum and then faded, pale orange stripe extending till hind margin of pronotum (Figs. 1-2). Pronotum with four transparent longitudinally parallel faded orange bands; mesonotum with two creamy white triangles at base. Eyes black, ocelli transparent. Forewing hyaline, one dark brown spot on third apical cell. Medium sized dorsoventrally depressed leafhoppers. Head including eyes narrower than pronotum; crown produced anteriorly, median length as long as width between eyes; ocelli on crown placed anteriorly, closer to eyes than to each other; coronal suture extending to 2/3 length of crown; frontoclypeus bulged at 1/3 rd, abruptly depressed posteriorly (Figs. 2-3); clypellus narrowed apically (Fig. 3); antennal ledges prominent; pedicel visible dorsally. Pronotum as long as wide; anterior margin convexly rounded, hind margin concave. Mesonotum wider than long. Male genitalia: Pygofer longer than wide; macrosetae on the posterior half (Figs. 6-7); ventral process well developed not branched, reaching anterior margin of pygofer (Figs. 7-8). Valve broader than long, posterior margin obtuse. Subgenital plate about 3.5X as long as broad at base, triangular, separate from valve, uniseriate macrosetae on the lateral margin (Fig. 9). Style short without preapical lobe, hair like setae subapically, apophysis rectilinear, apex truncate and maculose (Figs. 4-5). Connective inverted V-shaped (Fig. 10). Aedeagus short and stout, about as long as connective in lateral view, slightly curved anteriorly (Fig. 12) with pair of short teeth like lateral and median projections, lateral ledges prominent with median membranous region at apex, dorsal apodeme absent, gonopore subapical on caudal margin (Figs. 10-11). Measurements: Male 4.63mm long and 1.45mm wide across eyes. Material examined: HOLOTYPE ♂, India: Arunachal Pradesh: Basar, 661m, 27º58’39”N 94º41’31”E, 30.vi.2018, at light, Stuti & Tahseen R. Hashmi (NPC). PARATYPES 2♂, same data as holotype (NPC). Etymology: The species name “ dibangi ” refers to bamboo plant in local dialect. Remarks: Flatfronta dibangi sp. nov. closely resembles F. bella (the characters of F. bella in parenthesis) but differs as follows: aedeagal shaft in lateral view short and stout, with a pair of short teeth apical process (slender and long with one pair of long fine finger-like apical process), style apophysis truncate apically and preapical lobe absent (apophysis finger-like, rounded at apex, preapical lobe present).Published as part of M. Meshram, Naresh & Nikoshe, Akash P., 2020, Two new species of bamboo-feeding leafhopper genus Flatfronta (Hemiptera Cicadellidae, Deltocephalinae) from India, pp. 176-180 in Zootaxa 4758 (1) on pages 177-178, DOI: 10.11646/zootaxa.4758.1.8, http://zenodo.org/record/373091

    Flatfronta uttara M.Meshram & Nikoshe 2020, sp. nov.

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    Flatfronta uttara, sp. nov. Figs 13-22. Yellowish white, crown with orange longitudinal stripes one on either side of median line, pronotum with four longitudinal orange stripes. Mesonotum with basal triangles yellow, transverse suture and median narrow stripe on mesoscutellum fuscous (Fig. 13). Eyes grey, ocelli medium sized and transparent. Face with dorsal half of laterofrontal sutures and antennal ledges narrowly black. Forewing with two black spots one near claval vein, another on third apical cell. Medium sized, dorsoventrally depressed leafhoppers (Figs. 13–14). Head including eyes wider than pronotum; crown convexly produced anteriorly; median length slightly shorter than width between eyes, ocelli on anterior margin of crown, closer to eyes than to each other, coronal suture extending to 2/3 length of crown, frontoclypeus depressed, medially concave (Fig. 15); clypellus narrowed apically; antennal ledges prominent; antennal pedicel visible dorsally. Pronotum wider than long; anterior margin slightly wider than posterior; convexly rounded anteriorly, concave posteriorly. Mesonotum wider than long. Male genitalia: Pygofer depressed; longer than wide, membranous; macrosetae on caudoventral half with tuft of hair-like setae on postero-ventral region (Fig. 16), ventral pygofer process reaching half length of pygofer (Fig. 18), leaf like at apex, with lateral crenulate margin (Fig. 19). Subgenital plate triangular, about 3X as long as broad at base, separate from valve, uniseriate macrosetae on lateral margin (Fig. 20). Style short with prominent preapical lobe, with hair-like setae, apophysis digitate, with rounded apex (Fig. 17). Connective inverted V-shaped, fused with aedeagus (Fig. 21). Aedeagus 3X as long as connective, narrowed distally, strongly curved anteriorly in distal 1/3 (Fig. 22), without dorsal apodeme, gonopore apical (Fig. 22). Measurements: Male 4.01mm long and 1.01mm wide across eyes. Material examined: HOLOTYPE ♂, India: Uttarakhand: Pantnagar, 238m, 29º01’26”N 79º29’15”E, 10.iii.2018, at light, Rajgopal N.N. (NPC). Etymology: The species name “ uttara ” (Sanskrit, meaning North) refers to the Northern region of India where it was collected. Remarks: Flatfronta uttara sp. nov. closely resembles F. bella (the characters for F. bella in parenthesis) but differs as follows: 1. ventral pygofer process apex leaf like with lateral crenulate margin and reaching half length of the pygofer (pygofer process exceeding to anterior margin), 2. aedeagus sickle shaped, broad basally and narrowed apically (slender throughout with one pair of finger-like apical processes). FIG. (13–22) Flatfronta uttara sp. nov. 13–14. Habitus dorsal, lateral; 15. Face; 16. Style 17–19. Pygofer lateral, ventral, magnified pygofer process; 20. Subgenital plate with valve; 21–22. Aedeagus dorsal, lateral with Connective.Published as part of M. Meshram, Naresh & Nikoshe, Akash P., 2020, Two new species of bamboo-feeding leafhopper genus Flatfronta (Hemiptera Cicadellidae, Deltocephalinae) from India, pp. 176-180 in Zootaxa 4758 (1) on pages 178-179, DOI: 10.11646/zootaxa.4758.1.8, http://zenodo.org/record/373091

    Going Beyond Counting First Authors in Author Co-citation Analysis

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    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

    Variations on the Author

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    “Variations on the Author” discusses two of Eduardo Coutinho’s recent films (Um Dia na Vida, from 2010, and Últimas Conversas, posthumously released in 2015) and their contribution to the general question of documentary authorship. The director’s filmography is characterized by a consistent yet self-effacing form of authorial self-inscription: Coutinho often features as an interviewer that rather than express opinions propels discourses; an interviewer that is good at listening. This mode of self-inscription characterizes him as an author who is not expressive but who is nonetheless markedly present on the screen. In Um Dia na Vida, however, Coutinho is completely absent form the image, while Últimas Conversas, on the contrary, includes a confessional prologue that moves the director from the margins to the center of his films. This article examines the ways in which these works stand out in the filmography of a director who offers new insights into the notion of cinematic authorship

    Appropriate Similarity Measures for Author Cocitation Analysis

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    We provide a number of new insights into the methodological discussion about author cocitation analysis. We first argue that the use of the Pearson correlation for measuring the similarity between authors’ cocitation profiles is not very satisfactory. We then discuss what kind of similarity measures may be used as an alternative to the Pearson correlation. We consider three similarity measures in particular. One is the well-known cosine. The other two similarity measures have not been used before in the bibliometric literature. Finally, we show by means of an example that our findings have a high practical relevance.information science;Pearson correlation;cosine;similarity measure;author cocitation analysis

    Dispelling the Myths Behind First-author Citation Counts

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    We conducted a full-scale evaluative citation analysis study of scholars in the XML research field to explore just how different from each other author rankings resulting from different citation counting methods actually are, and to demonstrate the capability of emerging data and tools on the Web in supporting more realistic citation counting methods. Our results contest some common arguments for the continued use of first-author citation counts in the evaluation of scholars, such as high correlations between author rankings by first-author citation counts and other citation counting methods, and high costs of using more realistic citation counting methods that are not well-supported by the ISI databases. It is argued that increasingly available digital full text research papers make it possible for citation analysis studies to go beyond what the ISI databases have directly supported and to employ more sophisticated methods

    Author Index

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    koamabayili/VECTRON-author-checklist: VECTRON author checklist

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    We have done our best to complete the author checklist relating to the use of animals in the hut study. Note that the objective for the hut study was to evaluate the IRS treatment applications for residual efficacy against Anopheles mosquitoes, including the local An. coluzzii mosquito population. Cows were only used to attract mosquitoes into the huts and no tests were carried out directly on the cows. The author checklist is intended for use with studies where experiments are carried out on animals, which is why we have had such difficulty in completing this for the hut study, as many of the questions do not relate to how the cows were used
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