122,585 research outputs found

    Skejotettix muglingi Subedi 2022, comb. nov.

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    Skejotettix muglingi (Ingrisch, 2001b) comb. nov. (Figure 4) Previously reported as Coptotettix muglingi Ingrisch, 2001b (Pages 150–152, Figures 1–6) Type locality. Trishuli river near Mugling Bazar, river bed [27.86 o N, 84.56 o E] (Note: The coordinates are generated based on the locality mentioned in the original description of the species using Google Maps and represent an approximation of the locality). Materials examined. NEPAL • 1♀ (Figures 4 A-D); Gandaki Province, Tanahun District, Vyas Municipality, Buldikhola; 27.98745 o N, 84.29824 o E; 350 m a.s.l; 18 Mar. 2022; M. Subedi leg.; stream bank; collected by hand | NEPAL • 1♀ (Figures 4 E-H); Bagamati Province, Chitwan District, Kasara, Ghadiyal breeding center; 27.55362 o N, 84.33933 o E; 185 m a.s.l; 09 Jul. 2022; M. Subedi leg.; Manmade ponds amidst subtropical Sal forest; collected by hand | NEPAL • 1♀ (Figures 4 I-L); Lumbini Province, Kapilvastu District, Shivaraj Municipality, Umari, Tharu Museum; 27.69011 o N, 82.83008 o E; 155 m a.s.l; 30 Jul. 2022; M. Subedi leg.; Manmade ponds amidst human settlement area; collected by hand. Note: The type material was not examined directly, but rather examined with its images available in OSF along with the original description (Ingrisch 2001b) and compared with the materials at hand. Annotated specific diagnosis. This species has typical characters of Skejotettix gen. nov.: Brachynotal species with the upper point of insertion of antennal grooves at the lower level of compound eyes (in between the eyes in Coptotettix), reduced hindwings as well as intact nature of the median carina. Therefore, Coptotettix muglingi is very close to Skejotettix gen. nov. and does not belong to Coptotettix: I transfer this species to the genus Skejotettix gen. nov. However, Coptotettix does not have clear characters. So, a review is needed. Removing the species from Coptotettix is just one small step towards its natural organization.Published as part of Subedi, Madan, 2022, A new genus and a new groundhopper species from Nepal (Orthoptera: Tetriginae Skejotettix netrajyoti gen. et sp. nov.), pp. 35-54 in Zootaxa 5205 (1) on pages 41-43, DOI: 10.11646/zootaxa.5205.1.3, http://zenodo.org/record/728583

    Temnothorax buddha Subedi, Budha et Yusupov 2023, sp. n.

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    <i>Temnothorax buddha</i> Subedi, Budha et Yusupov, sp. n. <p>https://zoobank.org/NomenclaturalActs/ 76A25F96-B2D7-4AE1-8957-2B50F5B379A9</p> <p> TYPE MATERIAL. Holotype: worker (CDZMTU HymF121), <b>Nepal</b>: Bagmati Province, Shivapuri-Nagarjun National Park, Nagarjun Forest, Jamacho, 27.7452°N, 85.2667°E, 2094 m asl, bait collection, 3.V 2019, leg. I.P. Subedi. Paratype: 1 queen (CDZMTU HymF122), same data as a holotype.</p> <p> DESCRIPTION. WORKER. <i>Head.</i> In full-face view head slightly longer than broad (CI 1.26), with little rounded occipital corners and slightly convex or nearly straight posterior margin; anterior clypeal margin convex; eyes relatively large; mandibles elongate, masticatory margins with five teeth; antennae 12-segmented; scape almost reaches the posterior margin of head in full-face view (SI1 0.65, SI2 0.83). <i>Mesosoma.</i> In profile view, mesosoma with convex dorsum; promesonotal suture visible only ventrally, not reaching up to middle, metanotal groove shallow; propodeal spines moderately long, straight, slightly widened at the base, their tips are obliquely truncate; propodeal declivity roughly concave. <i>Petiole and postpetiole.</i> In profile, petiolar node longer than high with somewhat long anterior peduncle; petiolar node with steep and almost straight anterior face and convex, massive with sharpened corners dorsum; Postpetiole shorter than petiole with rounded dorsum and almost similar in height with petiole; in dorsal view broader than petiole, more or less equal in length and width itself. <i>Gaster.</i> Smooth and shiny. <i>Sculpture and pilosity</i>. Head dorsum with regular longitudinal striations extending to the occiput, frons and genae nearly smooth and shiny, mandibles with faint striations, coarse longitudinal and reticulate rugae in mesosoma, petiole, postpetiole and gaster with almost similar sculptures. Suberect to erect hairs covering the whole body, decumbent pubescent hairs on antennae and legs, dense in funicular segments of antennae. <i>Colour.</i> Body yellowish with little lighter legs and antennae, pilosity white.</p> <p>MEASUREMENTS AND INDICES. HL 0.67, HW 0.53, SL 0.44, OL 0.14, FRS 0.13, AL 0.79, AH 0.35, PNW 0.35, HTL 0.42, PL 0.31, PW 0.17, PH 0.21, PPL 0.22, PPW 0.24, PPH 0.21, ESL 0.14, CI 1.26, SI1 0.65, SI2 0.83, OI1 0.21, OI2 0.26, PI 1.47, PPI 1.07, AI 2.28, ESLI 0.26.</p> <p>QUEEN. Mostly similar with workers except usual modifications in the queen. Larger and more robust body with thick hair, mandibles almost triangular, striations as in workers, antennal scape almost reaching occipital border, large eyes, three distinct ocelli, gaster smooth and shiny with blackish yellow, body color yellowish with black tinge, legs and antennae faint yellow.</p> <p>MEASUREMENTS AND INDICES. HL 0.69, HW 0.60, SL 0.53, OL 0.17, FRS 0.14, AL 1.03, AH 0.47, PNW 0.50, HTL 0.44, PL 0.33, PW 0.19, PH 0.22, PPL 0.31, PPW 0.22, PPH 0.22, ESL 0.19, CI 1.16, SI1 0.76, SI2 0.88, OI1 0.24, OI2 0.28, PI 1.50, PPI 1.38, AI 2.18, ESLI 0.33.</p> <p>MALE. Unknown.</p> <p>BIONOMICS. These ants were collected from the cookie baits kept at Nagarjun Forest nearby Jamacho Monastery, Shivapuri-Nagarjun National Park, Nepal.</p> <p>DISTRIBUTION. It is reported only from Nagarjun forest, Shivapuri-Nagarjun National Park, Nepal.</p> <p>ETYMOLOGY. The species is named after the Lord Buddha who was born in Nepal.</p> <p> DIFFERENTIAL DIAGNOSIS. <i>Temnothorax buddha</i> sp. n. may be confused with Himalayan species such as <i>T</i>. <i>microreticulatus</i> Bharti et al., 2012, <i>T</i>. <i>pamiricus</i> (Ruzsky, 1902), <i>T</i>. <i>pakistanensis</i> Rasheed et al., 2020, and <i>T</i>. <i>himachalensis</i> Bharti et al., 2012, which also have unicolorous yellow body. But from the first species <i>T</i>. <i>buddha</i> sp. n. is distinguished by a more strongly sculptured and longer head (CI 1.26 <i>vs</i> max 1.17) and mesosoma, thinner propodeal spines, much rounded petiole node, shorter and broader petiolar peduncle and massive postpetiole. The new species differs from <i>T</i>. <i>pamiricus</i> and <i>T</i>. <i>himachalensis</i> in much longer propodeal spines, developed strong sculpture, petiole shape, etc. <i>T</i>. <i>buddha</i> sp. n. differs from <i>T</i>. <i>pakistanensis</i> in shorter head (CI 1.26 <i>vs</i> min 1.26 and max 1.32) and scape (SI1 0.65 <i>vs</i> min 0.72), absence of deep metanotal groove, longer propodeal spines, shape of petiole, and coarser sculpture of body.</p>Published as part of <i>Subedi, I. P., Yusupov, Z. M. & Budha, P. B., 2023, Three new species of the ant genus Temnothorax Mayr, 1861 (Hymenoptera: Formicidae, Myrmicinae) from Nepal, pp. 6-16 in Far Eastern Entomologist 475</i> on pages 7-10, DOI: 10.25221/fee.475.2, <a href="http://zenodo.org/record/8108848">http://zenodo.org/record/8108848</a&gt

    Skejotettix netrajyoti Subedi 2022, gen. et sp. nov.

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    Skejotettix netrajyoti gen. et sp. nov. Holotype (Figure 5). NEPAL • 1♀; Gandaki Province, Gorkha District, Gandaki Rural Municipality, Ghyalchok, Churlingtar; 27.80822 o N, 84.71922 o E; 460 m a.s.l; 4 June 2022; M. Subedi leg.; subtropical Sal forest; collected by hand; ANHM Paratypes (PT1, Figure 6). NEPAL • 1♀, 2 ♂; Gandaki Province, Gorkha District, Gandaki Rural Municipality, Ghyalchok, Churlingtar; 27.80822 o N, 84.71922 o E; 460 m a.s.l; 4 June 2022; M. Subedi leg.; subtropical Sal forest; collected by hand; ANHM Distribution. Subtropical Sal Forest, Churlingtar, Ghyalchok, Gorkha, Nepal (Figure 1G, H). Etymology. The specific epitheton is a Latinized noun in apposition referring to Shree Netrajyoti Basic School (Figure 1F) which lies adjacent to the type locality of the species. Vernacular name Skejo’s Salhopper Vernacular name etymology. Named after the dominant vegetation in the type locality, Sal (Shorea robusta). The name shows the association of the species to its habitat under the covers of Sal trees. Measurements. The key measurements of the holotype and the paratypes are presented in Table 2. Coloration. The coloration is cryptic, ranging from bright yellow to rusty brown with distinct (Figure 8A, B, C, E, F, H, I) or poorly marked (Figure 8D, G) post–humeral spots. Most of the individuals have uniform coloration on the pronotum (Figure 8B, C, D, E, G, H, I) while some may have differently colored halves of the pronotum (Figure 8A, F). Description (mainly of the female holotype). Head. Antenna. Filiform type; antennomeres: 16 in female and 15 in male (the apical segments are reduced and not clearly distinguished at 20x magnification when viewed under stereomicroscope, so the apical segment is assumed to have 2 apical segments); upper point of insertion of antennal grooves in level with lower margin of eye Frontal view. Vertex slightly narrower in width than an eye; paired lateral ocelli positioned between the compound eyes, about ¾ of a compound eye height from top; frontal costa bifurcates between compound eyes, above superior ocelli; frontal costa length above the bifurcation about ½ of a compound eye height; scutellum as wide as scapus with gradually widening towards the bottom; median ocellus situated far below the compound eyes, between facial carinae on the place where they end Lateral view. Head very slightly exserted above the pronotum; Frontal costa projecting in front of eyes rounded together with vertex but slightly concave above lateral ocelli Dorsal view. Vertex wider than a compound eye throughout the length; very slightly widening towards the base from the tip. Anterior margin of the fastigium of vertex truncated, very slightly indrawn in relation to the outer margin of the compound eye. Frontal costa distinctly produced in front of the anterior margin of the compound eyes; medial carina distinct, running to end of fossulae; fossulae deep, elongated, reaching almost to the base of the compound eye; lateral carinae raised to dorsal margin of eyes. Compound eyes do not reach upto the anterior margin of pronotum. Pronotum. Brachypronotal, reaching only around the mid-length of hind femora; surface granular or tuberculate. In frontal view, only lateral lobes are visible, directed downwards and slightly sideward.The rest of the pronotum is not visible because of the head. In lateral view whole pronotum is finely granulated, and smooth; the median carina is continuous through the whole pronotum length. Median carina has a slight elevation in the prozona and a weak depression after the prozona. The dorsal margin of the median carina distinctly undulated. Tip of the pronotum not covering the tip of the abdomen. Lateral lobes with truncated apex. The ventral sinus is deeper than the tegminal sinus. The humeroapical carina is short and striped, as well as the external lateral carina of the pronotum. The infrascapular area is long and with parallel margins. In the dorsal view, the anterior margin of the pronotum is truncated. Prozonal carinae is short and slightly diverging anteriorly; little curved inwards posteriorly. Humeral angle oblique; the tip of the pronotum angularly oblique. Internal lateral carina of the pronotum visible, ending 1 mm before the tip of the pronotum. Humeroapical spots are present (two dark spots). Wings. Tegmen. Well developed; Free part large, oblong Hind wings. Reduced, not reaching the apex of pronotal process Legs Fore legs. Setulose over the entire length; Femora. about 3.36 times long as wide; ventral margin finely serrated; Tibia. setose, dorsal and ventral margins faintly undulated; Tarsus. first segment short (dark brown to black in color), second segment elongated and bears claws. Mid legs. Femora . about 3.23 times long as wide; Tibia. setose, dorsal and ventral margins faintly undulated, ventral margin with large spines; Tarsus. first segment short (dark brown to black in color), second segment elongated and bears claws. Hind legs. Femora . robust, about 2.68 times long as wide, dorsal margin finely serrulate; Tibia. dorsal and ventral margins indistinctly to faintly undulated, ventral margin with large spines; Tarsus. first segment long (dark brown to black in color), bears pulvilli with tip spinose, second segment small, third elongated and bears claws. Differential diagnosis: The new species Skejotettix netrajyoti gen. et sp. nov. is similar to S. muglingi comb. nov.. The major differences are listed in Table 3.Published as part of Subedi, Madan, 2022, A new genus and a new groundhopper species from Nepal (Orthoptera: Tetriginae Skejotettix netrajyoti gen. et sp. nov.), pp. 35-54 in Zootaxa 5205 (1) on pages 43-50, DOI: 10.11646/zootaxa.5205.1.3, http://zenodo.org/record/728583

    Coptotettix coniopticus

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    Coptotettix coniopticus (Figure 12I–N) Previous records. Tellok, Taplejung (Chopard & Dreux 1966); Chyaubas (Bey-Bienko 1968) New record. NEPAL • 1 ♂ (Figure 12I, J, K); Gandaki Province, Gorkha District, Gandaki Rural Municipality, Ghyalchok, Tirtire khola; 27.80752 o N, 84.71823 o E; 420 m a.s.l; 19 May 2021; M. Subedi leg.; stream bank; collected by hand | NEPAL • 1 ♀ (Figure 12L, M, N); Gandaki Province, Gorkha District, Gandaki Rural Municipality, Ghyalchok, Churlingtar; 27.80822 o N, 84.71922 o E; 460 m a.s.l; 16 Jul. 2022; M. Subedi leg.; Subtropical Sal forest; collected by hand.Published as part of Subedi, Madan, 2022, A new genus and a new groundhopper species from Nepal (Orthoptera: Tetriginae Skejotettix netrajyoti gen. et sp. nov.), pp. 35-54 in Zootaxa 5205 (1) on page 52, DOI: 10.11646/zootaxa.5205.1.3, http://zenodo.org/record/728583

    Demirjian's 8 teeth method for Dental age estimation in Nepalese population

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    It is a dataset of the study conducted with objectives of applying Demirjian’s 8 teeth method to estimate age in the Nepalese Population. We had used the Orthopantomographs of Nepalese people of age above five and less than 23 years. The radiographs were compared to the ‘Tooth Development Chart’ and each tooth studied was assigned with any one of the 10 developmental stages using Demirijian’s 8 teeth method and total maturity scores determined from them

    Camponotus lasiselene Wang & Wu 1994

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    Camponotus lasiselene Wang & Wu, 1994 (fig. 4) M a t e r i a l s e x a m i n e d. Nepal: Kathmandu, Ranibari Community Forest [27.729444 N 85.3205555 E], 1310 m, pitfall collection, 13– 15.10.2019, 1 ♀ worker (IP Subedi, RP Pokhrel, S Subedi & A Subedi) (CDZMTU); idem, hand collection, 14.04.2021, 2 ♀ workers (IP Subedi, I Pandit & A Subedi) (CDZMTU). D i s t r i b u t i o n. Nepal (new record), China, Thailand, Vietnam. T a x o n o m i c n o t e s. Our worker specimen has an opaque black body with extremely abundant whitish short hairs, brownish red mandibles, antennae and tarsus, square-shaped head, short, broad and dorsally margined alitrunk, pronotum with acute margin, two plier-shaped propodeal spines and large, cylindrical gaster. The specimen was identified as C. lasiselene based on the species description and key in Wang & Wu (1994). C. lasiselene is very close to Fig. 4. Camponotus lasiselene. C. selene in the color, shape and sculpture of the body but has abundant whitish erect hair on the body (Wang & Wu, 1994).Published as part of Subedi, I. P., Budha, P. B., Bharti, H., Alonso, L. & Yamane, S., 2021, First Record Of The Ant Subgenus Orthonotomyrmex Of The Genus Camponotus From Nepal (Hymenoptera, Formicidae), pp. 279-284 in Zoodiversity 55 (4) on pages 281-282, DOI: 10.15407/zoo2021.04.279, http://zenodo.org/record/637784

    CD16a with oligomannose-type N-glycans is the only “low-affinity” Fc γ receptor that binds the IgG crystallizable fragment with high affinity in vitro

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    Fc γ receptors (FcγRs) bind circulating IgG (IgG1) at the surface of leukocytes. Antibodies clustered at the surface of a targeted particle trigger a protective immune response through activating FcγRs. Three recent reports indicate that the composition of the asparagine-linked carbohydrate chains (N-glycans) of FcγRIIIa/CD16a impacted IgG1-binding affinity. Here we determined how N-glycan composition affected the affinity of the “low-affinity” FcγRs for six homogeneous IgG1 Fc N-glycoforms (G0, G0F, G2, G2F, A2G2, and A2G2F). Surprisingly, CD16a with oligomannose N-glycans bound to IgG1 Fc (A2G2) with a KD = 1.0 ± 0.1 nM. This affinity represents a 51-fold increase over the affinity measured for CD16a with complex-type N-glycans (51 ± 8 nM) and is comparable with the affinity of FcγRI/CD64, the sole “high-affinity” FcγR. CD16a N-glycan composition accounted for increases in binding affinity for the other IgG1 Fc glycoforms tested (10–50-fold). This remarkable sensitivity could only be eliminated by preventing glycosylation at Asn162 with an Asn-to-Gln mutation; mutations at the four other N-glycosylation sites preserved tighter binding in the Man5 glycoform. None of the other low-affinity FcγRs showed more than a 3.1-fold increase upon modifying the receptor N-glycan composition, including CD16b, which differs from CD16a by only four amino acid residues. This result indicates that CD16a is unique among the low-affinity FcγRs, and modifying only the glycan composition of both the IgG1 Fc ligand and receptor provides a 400-fold range in affinities.This research was originally published in the Journal of Biological Chemistry. Subedi, Ganesh P., and Adam W. Barb. "CD16a with oligomannose-type N-glycans is the only “low-affinity” Fc γ receptor that binds the IgG crystallizable fragment with high affinity in vitro." Journal of Biological Chemistry 293, no. 43 (2018): 16842-16850. © the Author(s). doi: 10.1074/jbc.RA118.004998.</p

    Coptotettix annandalei Hancock 1915

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    Coptotettix annandalei (Figure 12A–H) Previous records. Chaubas, Kabhrepalanchok (Bey–Bienko 1968); near Nagarkot, Bhaktapur (Balderson & Yin 1987); east of Pokhara, Kaski; Mugling Bazar, Chitwan; Jugedi, Chitwan; Gaidacamp, Chitwan (Ingrisch 1987) New record. NEPAL • 1 &male; (Figure 12E, F), 1 &female; (Figure 12C, D); Gandaki Province, Gorkha District, Gandaki Rural Municipality, Ghyalchok, Churlingtar; 27.80822 o N, 84.71922 o E; 460 m a.s.l; 24 Jun. 2021; M. Subedi leg.; Subtropical Sal forest; collected by hand | NEPAL • 1 &male; (Figure 12G, H), 1 &female; (Figure 12A, B); Gandaki Province, Gorkha District, Gandaki Rural Municipality, Ghyalchok, Bhottar khola; 27.80547 o N, 84.72615 o E; 445 m a.s.l; 28 Mar. 2022; M. Subedi leg.; Rain fed stream amidst subtropical Sal forest; collected by hand. Discussion. The morphology of the specimens observed agrees with the original description of Coptotettix annandalei. Two different variations in color as mentioned in the original description were also observed: dark grey in the individuals from the rainy season of monsoon (Figure 12C, D, E, F), and paler grey marked with light yellow on the pronotum and hind femora in the individuals from the dry season prior to monsoon (Figure 12A, B, G, H). These forms are well adapted to match the surrounding colors which provide a degree of protection against potential predators and may be considered as wet season and dry season forms.Published as part of Subedi, Madan, 2022, A new genus and a new groundhopper species from Nepal (Orthoptera: Tetriginae Skejotettix netrajyoti gen. et sp. nov.), pp. 35-54 in Zootaxa 5205 (1) on page 51, DOI: 10.11646/zootaxa.5205.1.3, http://zenodo.org/record/728583

    Fig. 2 in Three new species of the ant genus Temnothorax Mayr, 1861 (Hymenoptera: Formicidae, Myrmicinae) from Nepal

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    Fig. 2. Temnothorax buddha sp. n., queen, paratype. A – habitus, profile view; B – head,Published as part of Subedi, I.P., Yusupov, Z.M. & Budha, P.B., 2023, Three new species of the ant genus Temnothorax Mayr, 1861 (Hymenoptera: Formicidae, Myrmicinae) from Nepal, pp. 6-16 in Far Eastern Entomologist 475 on page 9, DOI: 10.25221/fee.475.2, http://zenodo.org/record/810884

    A Multi-Language Comparison of Influences on Author Verification using Character N-Grams

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    We create a new multi-language corpus for author verification based on Wikipedia talkpages, and evaluate the influence that differences in topic and time have on character n-gram author profiles. Topic alignment between two texts is found to increase author verification precision, and an authors writing style is found to change over time, but not more significantly after 3 years than after 1 year.Information ArchitectureWISElectrical Engineering, Mathematics and Computer Scienc
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