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FIGURE 9. Thoracic sternites showing vulvae, A in A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871)
No full textFIGURE 9. Thoracic sternites showing vulvae, A. Badistemon turgidulum (Alcock, 1909), Paralectotype female (ZSI-C6952/2) (cw 30.2 mm × cl 24 mm); B. B. pealianus (Wood-Mason, 1871) comb. nov. Paratype female (ZSI-C6413/3) (cw 37.2 mm × cl 28.9 mm)Published as part of Mitra, Santanu, Monica, Thingbaijiam & Waikhom, Mema Devi, 2020, A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871), pp. 475-490 in Zootaxa 4838 (4) on page 487, DOI: 10.11646/zootaxa.4838.4.2, http://zenodo.org/record/440536
FIGURE 6 in A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871)
No full textFIGURE 6. Badistemon turgidulum (Alcock, 1909), lectotype male (ZSI-C6952/2) (cw 28.7 mm × cl 23.5 mm): A. dorsal view of carapace; B. frontal view of cephalothorax; C. male thoracic sternum and pleon.Published as part of Mitra, Santanu, Monica, Thingbaijiam & Waikhom, Mema Devi, 2020, A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871), pp. 475-490 in Zootaxa 4838 (4) on page 484, DOI: 10.11646/zootaxa.4838.4.2, http://zenodo.org/record/440536
FIGURE 5. Badistemon fulvum n in A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871)
No full textFIGURE 5. Badistemon fulvum n. sp., holotype male (ZSI-C7543/2) (cw 48.7 mm × cl 39.5 mm): A. dorsal view of right G1; B, ventral view of left G1; C, dorsal view of right G2. Scale bar=2 mm.Published as part of Mitra, Santanu, Monica, Thingbaijiam & Waikhom, Mema Devi, 2020, A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871), pp. 475-490 in Zootaxa 4838 (4) on page 483, DOI: 10.11646/zootaxa.4838.4.2, http://zenodo.org/record/440536
Badistemon Yeo & Ng 2007
No full textKey to the species of Badistemon Yeo & Ng, 2007 1. Suture between male thoracic sternites s3/s4 is prominent; sixth pleonal somite ca. 2.5 times wider than median length; telson elongated, distal end narrowing; G1 subterminal segment distal part relatively broad, slightly narrower than basal width, terminal segment relatively shorter, ca. 0.32 times than combined length of subterminal segment and flexible joint (Fig. 6 A–C, 8 A–C; Yeo & Ng, 2007: fig. 4. a–e)........................................ B. turgidulum (Alcock, 1909) (Myanmar) - Male thoracic suture between s3/s4 is not prominent, represent as a small depression in lateral margin of sternites; sixth pleonal somite note more than ca. 2 times wider than median length; telson elongated, distal end narrowing; G1 subterminal segment distal part neck-like, abruptly narrower than basal width, terminal segment relatively long, more than ca. 0.40 times than combined length of subterminal segment and flexible joint........................................................ 2 2. Cervical groove prominent, regions distinct (Fig. 7A), male telson as long as broad (Fig. 7C), G1 terminal segment sub-cylindrical, tip truncated (Fig. 8 D–F; Wood–Mason, 1871: pl. 14, fig.7)..... B. pealianus comb. nov. (Assam & Mizoram, India) - Cervical groove superficial, regions not distinct (Fig. 2A), male telson broader than long (Fig. 2 C), G1 terminal segment conical, tip pointed (Fig. 4 A–D, 5A, B)............................................ B. fulvum sp. nov. (Manipur, India)Published as part of Mitra, Santanu, Monica, Thingbaijiam & Waikhom, Mema Devi, 2020, A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871), pp. 475-490 in Zootaxa 4838 (4) on page 489, DOI: 10.11646/zootaxa.4838.4.2, http://zenodo.org/record/440536
Badistemon fulvum Mitra & Monica & Waikhom 2020, sp. nov.
No full textBadistemon fulvum sp. nov. (Figs. 2–5, 10 A) Material examined. Holotype: male (cw 48.7 mm, cl 39.5 mm, ch 22.8 mm, fw 11.9 mm), from Bungkucha stream, Bungpa Khunou village, Kamjong District, Manipur, north-east India (24°48´45.93″N; 94°28´23.41″E), altitude 997 m, 22 nd July 2018, coll. Thingbaijiam Monica (ZSI-C7543 /2). Paratype: 1 female (cw 31.4 mm, cl 22.8 mm, ch 13.8 mm, fw 9.5 mm), collection data same as above (ZSI-C7544/2). Comparative material: Potamon turgidulum Alcock, 1909, lectotype (designated herein): male (28.7 × 23.5 mm); paralectotypes 6 males (cw 24.2–26.3 mm × cl 21.5–22.4 mm) and 1 female (cw 30.2 mm × cl 24 mm), Burma, coll. W. Theobald (ZSI-C 6952 /3). Potamon (Potamon) pealianum (Wood-Mason, 1871), 1 male, holotype (cw 41.6 mm, cl 35.2 mm, ch 18.8 mm, fw 10.4 mm), Sivasagar, Assam; coll. S. E. Peal (ZSI-C6958 /3); 2 females (cw 38.2–45.8 mm, cl 33.1–39.4 mm, ch 8.9–15.7 mm), Sivasagar, Assam; coll. S. E. Peal (ZSI-C6413 /3). 1 male (cw 47.1 mm, cl 38.4 mm, ch 14.7 mm, fw 11.5 mm), Kakhyen hills, Myanmar, 20 february, 1875; coll. J. Anderson (ZSI-C6915 /3). 1 female (cw 43.6 mm, cl 32.7 mm, ch 16.2 mm), Bokpui village, Lunglei District, Mizoram, India; 19 October, 2103; coll. S. Mitra (ZSI-C6117 /2). Diagnosis. Carapace subquadrate, distinctly broader than long, longitudinally convex, dorsal surface glabrous; anterolateral margin longer than posterolateral margin, epigastric cristae well developed, rugose, separated by post orbital cristae by distinct groove, postorbital cristae sharp, confluent with epibranchial tooth (Fig. 2A); cornea relatively large (Fig. 2B); male pleon broadly triangular, pleonal somite 6 trapezoidal in shape (Fig. 2C), exopod of third maxilliped with flagellum, longer than ca. 0.5 times of merus width; G1 terminal segment relatively long, outwardly bent, subcylindrical with low dorsal flap, tip pointed, groove for G2 terminal; G2 long, almost straight, terminal segment distinctly longer than ca. 0.5 times length of basal segment (Fig. 4 A–E, 5A–C). Description. Holotype male, carapace broader than long (cw/cl=1.2), longitudinally convex, high (ch/cl=0.6); dorsal surface glabrous, anterolateral margin convex, serrated, converging posteriorly, longer than posterolateral margin (Fig. 2A); posterolateral margin gently converging towards posterior border, with short, oblique striae (Fig. 2A); front relatively broad, width ca. 0.29 times maximum carapace width, distinctly deflexed ventrally, frontal margin slightly bilobed (Fig. 2B); Epigastric cristae well developed, rugose, separated by postorbital cristae by distinct groove; postorbital cristae sharp, confluent with epibranchial tooth; external orbital angle well developed, outer margin distinctly convex, ca. 2 times longer inner margin; epibranchial tooth small, sharp, separated from external orbital angle by a distinct cleft; branchial region with some low granules, frontal region with bilobed eminence immediately behind and parallel of frontal margin, clearly divided by gastric groove; orbital region narrow, smooth, concave; regions behind epigastric and postorbital cristae smooth; gastric and branchial region inflated; cervical groove ‘S’- shaped, shallow, superficial, mesogastric groove long, bifurcated posteriorly, H- shaped groove prominent, cardiac groove deep (Fig. 2A); pterygostomial region smooth, frontal median triangle incomplete with dorsal margin only, posterior margin of epistome with triangular median tooth, outer margin sloping downwards laterally; orbital margin sub-triangular, eyes with large cornea, antennae short reaching up to base of eye stalk, antennules long, antennular fossae quadrangular. Mandibular palp 3 segmented, terminal segment simple, first and second maxilliped has long flagellum on exopod, ischium of third maxilliped subrectangular, almost twice as long as broad, median sulcus prominent, merus as long as broad, almost pentagonal (Fig. 2B); exopod long, reaching distal third of merus length, gradually narrower from base to proximal part, flagellum well developed, reaching more than half of merus width. Chelipeds smooth, glabrous, unequal, right cheliped stouter than left, all margins of merus distinctly serrated, proximal inner margin of merus with sharp tooth, carpus rugose, sunken antero-medially, carpus with a long stout inner distal tooth followed by short basal tooth; pollex of major cheliped with 2 large triangular tooth on its cutting edge, dactylus almost smooth, except basal part with 3 small sharp teeth; palm larger than dactylus, inner and outer surface inflated, 4 sharp serration on dorsal surface of palm, inner and lateral margins of merus serrated, distal part of inner border of merus with slender strong tooth; ambulatory legs long, slender, p3 longest, ca. 1.5 of carapace width, p3 and p4 longer than cheliped, upper margin of merus of p2 to p5 with sub-distal spine, p3 and p4 propodus is longer than ca. 2.5 of width, dactylus distinctly longer than propodus, gently curved (Fig. 2A). Thoracic sternites smooth, glabrous, pitted, suture between thoracic sternite s1/s2 indistinct, suture between thoracic sternites s2/s3 distinct, deep broad groove, not reaching to lateral margin, suture between thoracic sternite s3/s4 visible as small notch on lateral margins, followed by indistinct shallow depression (Fig. 2C); suture s7/s8 shallow, interrupted by longitudinal median groove between s7 and s8, lacking transverse ridge; Pleonal locking mechanism with prominent tubercle, sharply pointed towards ventral side, on lower part of s5; sternopleonal cavity deep, long, reaching up to imaginary line joining median part of cheliped coxae. Pleon triangular, pleonal somite 3 widest, somite 6 trapezoidal, proximal width nearly twice than median length, distinctly longer than preceding somites, shorter than telson; telson broadly triangular, proximal width broader than long, lateral margin concave, apex rounded (Fig. 2C). G1 terminal segment slender, relatively long, ca. 0.4 times combined length of flexible joint and subterminal segments, almost cylindrical, tip triangular, pointed, bent outwards, tip not reaching pleonal locking tubercle; low dorsal flap on outer middle part of terminal segment; subterminal segment stout, basal 1/3 distinctly broad, outer margin straight, remaining 2/3 of subterminal segment gradually narrowing, distal end neck-like, bent outwards, groove for G2 terminal; G2 slender, almost straight, terminal segment more than half of subterminal segment (Figs. 4 A–E, 5A–C). Female pleon narrowly ovate in outline, all sternites are not fully covered by the pleon (Fig. 3C). The pleonal somite 1 is short, pleonal somites 2-5 are progressively longer, and the pleonal somite 6 is the longest, shorter than the telson, with convex lateral margins (Fig. 3C). The telson is broadly triangular, much broader than long, with strongly convex lateral margins (Fig. 3C); suture between s3/s4 are not discernible (Fig. 3C), the vulvae broader than long, large, oblong ovate, directed towards ventro-medial directions, located on the thoracic sternite s6, with the distal edge touching the suture s5/s6, lower half covered by sternal cover (Fig. 3D). Variation. The female paratype (ZSI-C7544/2) is not ovigerous and shares most of the non-sexual characters with the holotype male, except some characters: carapace grooves and regions are relatively more prominent, chelipeds subequal (Fig. 3A) (vs. carapace grooves and regions relatively less distinct, chelipeds unequal in male holotype (Figs. 2A, 10A); epistomal median tooth blunt (Fig. 3B) (vs. epistomal median tooth sharply pointed in male (Fig. 2A). Live colouration. In the male holotype, the carapace is chestnut brown, chelipeds outer parts orange yellow, ventral parts ivory white; frontal margin, epigastric cristae, post orbital cristae and orbital margins are golden yellow (Fig. 10 A); carapace of the female paratype dark brown, chelipeds pale brown, propodus orange-yellow, fingers ashy grey, tip of fingers yellow, third maxilliped ischium with conspicuous brown and white longitudinal stripes. Etymology. The new species is named after its golden yellow carapace margins, frontal margin, orbital margin and epistome, the name is derived from Latin ‘Fulvus’ means-‘golden yellow’; gender neuter. Type locality. Bungkucha stream (24°48´45.93″N; 94°28´23.41″E), Bungpa Khunou village, Kamjong District, Manipur, India Remarks. The present new species, collected from Manipur, India, is adjacent to Myanmar and morphologically agrees with Badistemon, as presently defined, i.e. relatively high, squarish-looking carapace, quite broader than long; epigastric and postorbital cristae well developed, third maxilliped exopod with long flagellum not exceeding merus width, ambulatory legs slender, long; male abdomen narrowly triangular and the G1 slender, terminal segment with low dorsal flap (Fig. 4 A–D). Badistemon fulvum n. sp. is distinguished from B. turgidulum (Alcock, 1909) by the following morphological characters: suture between thoracic sternites s2/s3 distinct, deep broad groove, not reaching up to lateral margins (Fig. 2C) (vs. suture between thoracic sternites s2/s3 narrow, groove shallow reaching up to lateral margins in B. turgidulum; cf. Yeo & Ng 2007: fig. 4 c; Fig. 6B); suture between thoracic sternites s3/s4 not discernible in new species (Fig. 2 C) (vs. suture between sternite s3/s4 distinct, represent as oblique shallow groves towards abdominal cavity; Yeo & Ng, 2007: fig. 4 c; Fig. 6C); telson broadly triangular, proximal width distinctly broader than long in B. fulvum n. sp. (Fig. 2C) (vs. telson as long as broad in B. turgidulum; cf. Alcock, 1910: pl 2, 5 a; Yeo & Ng, 2007 fig. 4c; Fig. 6C); G1 subterminal segment distal part neck-like, abruptly narrower than basal width; terminal segment subconical, relatively long, ca. 0.4 times than combined length of subterminal segment, tip pointed in B. fulvum n. sp. (Fig. 4 A–D, 5A–C) (vs. G1 subterminal segment distal width slightly narrower than basal width; terminal segment subcylindrical, relatively short, ca. 0.32 times than combined length of subterminal segment and flexible joint, tip broad and blunt in B. turgidulum; cf. Yeo & Ng, 2007: fig. 4d, e; Fig. 8A, B); flexible zone elongated with triangular median lobe in B. fulvum n. sp. ( Figs. 4B, D; 5A ); flexible zone short with a small, blunt median lobe in B. turgidulum; cf. Yeo & Ng, 2007: fig.4 d, e; Fig. 8 A); G2 terminal part straight, terminal part nearly half length of subterminal part in B. fulvum n. sp. (Fig. 4E, 5C) (vs. G2 terminal part twisted, terminal part slightly longer than half of subterminal part in B. turgidulum; Fig. 8C); In female, the vulvae large, oblong, directed ventro-medially, situated just below the suture between the fifth and sixth sternites, lower half covered by sternal cover in B. fulvum n. sp. (Fig. 3D) (vs. in female, vulvae is relative more rounded, directed towards longitudinal median groove, lower 1/3 only covered by sternal cover in B. turgidulum; Fig. 9A). The new species has several morphological similarities with Badistemon pealianus (Wood-Mason, 1871) comb. nov. as both the species have a high, roughly quadrangular carapace, broad front, relatively long ambulatory legs, third maxilliped ischium broadly rectangular, with longitudinal median sulcus, the exopod with well developed flagellum not more than merus width, male sterno-pleonal cavity barely exceeding imaginary line jonining posterior edge of cheliped base, and G1 terminal segment relatively long, setose with low, short dorsal flap, G2 straight with terminal segment more than half of subterminal segment. The new species differs from B. pealianus, in the following morphological characters: Telson distinctly broader than long in B. fulvum n. sp. (Fig. 2 C) (vs. telson as long as broad in B. pealianus; Fig. 7 C); the external orbital tooth outer margin is almost straight to slightly convex in B. fulvum n. sp. (Fig. 2A) (vs. external orbital tooth outer margin relatively more convex in B. pealianus; Fig. 7 A); epibranchial tooth short, broad based, pointed laterally in B. fulvum n. sp. ( Fig. 2 A) (vs. epibranchial tooth short, base narrow, frontally pointed; Fig. 7 A); cervical groove superficial in B. fulvum n. sp. (Fig. 2A) (vs. cervical grooves are distinct in B. pealianus; Alcock, 1910: pl 10. fig. 44; Fig. 7 A); terminal segment of the G1 tapered toward the tip in the new species (Fig. 4 A–D, 5 A, B) (vs. G1 terminal segment subcylindrical, tip truncated in B. pealianus; Fig. 8. D, E); female vulvae oblong shaped, occupied slightly less than half of the length of sixth sternite in B. fulvum n. sp. (Fig. 3D), (vs. vulvae is ovate, relatively large, occupied more than half of the length of sixth sternite in B. pealianus; Fig. 9B). Ecological notes. The crabs were collected from Bungpa Khunou, at Kamjong District, Manipur, northeast India. Bungpa Khunou is a small village in Kamjong subdistrict head quarter, which was previously under Ukhrul District near the Indo-Myanmar border (Fig.1). The crabs are collected from the Bungkucha stream (Fig. 10B, C), it ends in the Angkekung river. This stream is seasonal, almost dried up in summer season. The area is in a secondary forest is almost free from anthropogenic disturbance, as the local people of this place do not depend entirely on forest resources. According to the local people, during the rainy season the crabs come up to the foothills, from the river. Crabs make their nest holes in soft soils under the small stones beside the stream. Geographical distribution. B. fulvum n. sp. is so far only recorded from its type locality at Bungpa Khunou village, Kamjong District, Manipur, India.Published as part of Mitra, Santanu, Monica, Thingbaijiam & Waikhom, Mema Devi, 2020, A new species of freshwater crab of the genus Badistemon Yeo & Ng, 2007 (Decapoda: Brachyura: Potamidae: Potamiscinae) from Manipur State, India with the reassignment of Potamiscus pealianus (Wood-mason, 1871), pp. 475-490 in Zootaxa 4838 (4) on pages 476-482, DOI: 10.11646/zootaxa.4838.4.2, http://zenodo.org/record/440536
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
Variations on the Author
Get PDF“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
Get PDFWe 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
Get PDFWe 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
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