95,794 research outputs found
The Folio: F. C. C. Magazine
Maqbool Ahmad Bhatty-Editorial-Before We Part. pp. 1-2; Adya Sharan Sharma-Article-Swami Ram Tirtha. pp. 2-4; B. R. P.-The Master of My Ruined Garden. pp. 4; Ayoob Ali-Art. pp. 4-5; Gilani, S. A. S.-Poetry-The Sacred Shrine. pp. 5-6; Anupam Dhar-Kashmiri Marriages. pp. 6-8; Nazir Latif-The Bookworm. pp. 8; Hans-Article-Study of Macbeth as a Tragic Hero. pp. 9-10; Laroia, V. K.-Professional Error. pp. 10-11; Saran Singh-The Days of Our Glory. pp. 11-12; Manmohan Mehta-Article-The Short Story in England. pp. 12-13; [Hindi]. 4 p.; Punjabi Phulvari [Punjabi]. 4 p.; The Folio [Urdu]. 6 p.Dr. C. H. Rice, M.A., Ph.D., LL.D., Vice Chancellor, University of the Punjab. after page 1
Paktongius thaiensis Klementz & Sharma 2023, comb. nov.
<i>Paktongius thaiensis</i> (Suzuki, 1985) comb. nov. <p> <i>Mysorea thaiensis</i> Suzuki, 1985, p. 102 –104, fig. 19, Table 15; Zhang & Zhang, 2015, p. 336 –341, figs. 1–25, table 1.</p> <p> <i>Material examined.</i> ♂ (MCZ-92256/ MCZ DNA104859) THAILAND, Sakon Nakhon, Phu Phan National Park (16°48.63’N, 103°53.59’E), 1-4.vi. 2007, 522 m, dry evergreen forest near house, <i>leg.</i> W. Kongnara.</p> <p> <i>Diagnosis.</i> Distinguished from congeners by the combination of the following characters: (1) anal plate with three large spines; (2) free tergite III with a transverse row of six tubercles; (3) scutal areas II-V with two median tubercles at posterior margin; (4) tarsal formula 5:9:6:6.</p> <p> <i>Distribution.</i> Known from: Chiang Mai (Suzuki 1985) and Sakon Nakhon Provinces, Thailand; Champasak Province, Laos (Zhang & Zhang 2015) (Fig. 12).</p>Published as part of <i>Klementz, Benjamin C. & Sharma, Prashant P., 2023, New species of Paktongius and convergent evolution of the gonyleptoid-like habitus in Southeast Asian Assamiidae (Opiliones: Laniatores), pp. 34-54 in Zootaxa 5389 (1)</i> on page 51, DOI: 10.11646/zootaxa.5389.1.2, <a href="http://zenodo.org/record/10404551">http://zenodo.org/record/10404551</a>
The Folio: F. C. C. Magazine
Sharma, O. P.-Editorial. pp. 1-2; Strickler, H. J.-Speech-Treasure, New and Old. pp. 2-10; Sir Maharaj Singh-Speech-Convocation Address. pp. 10-13; Pasricha, K. L.-Speech-Valedictory Address. pp. 14-16; Velte, F. M.-Article-The Place of Sport in our Colleges. pp. 16-21; Sharma, O. P.-Poetry-A Call to the Spirit. pp. 21; Letters to the Editors. pp. 22-25; Singh, V. Z.-Poetry-The First Signs. pp. 25; Thoughts on the Eve of New Year. pp. 25-27; Creighton, W.-Co-Eds'Corner. pp. 27-28; Sharma, O. P.-The Fifteen. pp. 28-31; Societies. pp. 31-35; News & Notes. pp. 35-36; Halls of Residence. pp. 36-38; Sports. pp. 38-39; Obituary. pp. 39-40; Poetry-An Elegy. pp. 40; [Hindi]. 16 p.; The Folio [Urdu]. 16 p.The Fifteen 1941-42. after page 3
Concomitant formation of differently coordinated copper(II) complexes in the same reaction: Structural studies of [trans-Cu(γ-picoline) 2(H 2O) 4](p-toluene sulfonate) 2·2H 2O and [trans-Cu(γ-picoline) 4](p-toluenesulfonate) 2·2H 2O
Two new copper(II) complexes comprising of coordinated and non-coordinated p-toluenesulfonate, [trans-Cu(γ-pic) 2(H 2O) 4](pts) 2·2H 2O, 1 and [trans-Cu(γ-pic) 4(pts) 2]·2H 2O, 2 (where p-toluenesulfonate = pts and γ-picoline = γ-pic) have been isolated from the same reaction mixture. These complexes have been characterized by spectroscopic techniques, molar conductance, TGA, magnetic susceptibility studies, and single crystal X-ray structure determination. Both complexes crystallize in the monoclinic crystal system with P2 1/c space group having cell dimensions of a = 8.0203(2) , b = 19.4471(4) , c = 10.3000(3) , β = 93.4420(9)°, V = 1603.61(7) 3, (Z = 2) in 1 and a = 10.1473(2) , b = 10.9948(2) , c = 18.0952(5) , β = 93.0340(9)°, V = 2015.96(8) 3, (Z = 2) in 2. Single -crystal X-ray structure determinations revealed the presence of ionic complex, viz: one complex cation [trans-Cu(γ-pic) 2(H 2O) 4], two pts anions and two water molecules of crystallization in the complex 1 and neutral [trans-Cu(γ-pic) 4(pts) 2] and two water molecules of crystallization in 2. The crystal packing in both complexes is stabilized by OH⋯O, CH⋯O hydrogen bonds and CH⋯π interactions
Measurement of the ratio of prompt χ c to J / ψ production in pp collisions at √s = 7 TeV
The prompt production of charmonium χ c and J / ψ states is studied in proton-proton collisions at a centre-of-mass energy of √s = 7 TeV at the Large Hadron Collider. The χ c and J / ψ mesons are identified through their decays χ c → J / ψ γ and J / ψ → μ + μ - using 36 pb - 1 of data collected by the LHCb detector in 2010. The ratio of the prompt production cross-sections for χ c and J / ψ, σ (χ c → J / ψ γ) / σ (J / ψ), is determined as a function of the J / ψ transverse momentum in the range 2 < p T J / ψ < 15 GeV / c. The results are in excellent agreement with next-to-leading order non-relativistic expectations and show a significant discrepancy compared with the colour singlet model prediction at leading order, especially in the low p T J / ψ region
Paratylenchus prunii Sharma, Sharma & Khan 1986
<i>Paratylenchus prunii</i> Sharma, Sharma & Khan, 1986 Esmaeili & Heydari 2017: <p> 10♀: L = 324 (290–343) µm; <i>a</i> = 21.8 (20.3–23.2); <i>b</i> = 3.1 (3.0–3.5); <i>c</i> = 12.8 (10.7–17.5); St = 26.1 (24.0– 28.0) µm; V = 81 (79–83)</p> <p> 2♂: L = 275, 290 µm; <i>a</i> = 19.3, 21.2; <i>c</i> = 12.6, 13.8; Spicules = 14, 15 µm</p> <p>Associated plant and locality: Grapevine from Kermanshah (Esmaeili & Heydari 2 0 17 [F])</p>Published as part of <i>Ghaderi, Reza, Karegar, Akbar, Miraeiz, Esmaeil & Hesar, Abbas Mokaram, 2019, An updated and annotated checklist of the Tylenchulidae (Nematoda: Criconematoidea) of Iran, pp. 205-229 in Zootaxa 4545 (2)</i> on page 213, DOI: 10.11646/zootaxa.4545.2.3, <a href="http://zenodo.org/record/2618787">http://zenodo.org/record/2618787</a>
On the structure and origin of pressure fluctuations in wall turbulence: predictions based on the resolvent analysis
We generate predictions for the fluctuating pressure field in turbulent pipe flow by re-formulating the resolvent analysis of McKeon & Sharma (2010) in terms of the so-called primitive variables. Under this analysis, the nonlinear convective terms in the Fourier-transformed Navier-Stokes equations are treated as a forcing that is mapped to a velocity and pressure response by the resolvent of the linearized Navier-Stokes operator. At each wavenumber-frequency combination, the turbulent velocity and pressure field are represented by the most-amplified (rank-1) response modes, identified via a singular value decomposition of the resolvent. We show that these rank-1 response modes reconcile many of the key relationships between the velocity field, coherent structure (i.e., hairpin vortices), and the high-amplitude wall-pressure events observed in previous experiment and DNS. A Green’s function representation shows that the pressure fields obtained under this analysis correspond primarily to the fast pressure contribution arising from the linear interaction between the mean shear and the turbulent wall-normal velocity. Recovering the slow pressure requires an explicit treatment of the nonlinear interactions between the Fourier response modes. By considering the velocity and pressure fields associated with the triadically-consistent mode combination studied by Sharma & McKeon (2013), we identify the possibility of an apparent amplitude modulation effect in the pressure field, similar to that observed for the streamwise velocity field. However, unlike the streamwise velocity, for which the large scales of the flow are in phase with the envelope of the small-scale activity close to the wall, we expect there to be a ?/2 phase difference between the large scale wall-pressure and the envelope of the small-scale activity. Finally, we generate spectral predictions based on a rank-1 model assuming broadband forcing across all wavenumber-frequency combinations. Despite the significant simplifying assumptions, this approach reproduces trends observed in previous DNS for the wavenumber spectra of velocity and pressure, and for the scale-dependence of wall-pressure propagation speed
Paktongius paritensis Klementz & Sharma 2023, sp. nov.
<i>Paktongius paritensis</i> sp. nov. <p>(Figs. 7–8, 11, 12; Table 5)</p> <p> <i>Type material.</i> <i>Holotype.</i> ♀ (MHNG), MALAYSIA, Pahang, Cameron Highlands, Tanah Rata, near Parit Falls, 4°28.52’N, 101°23.02’E, ca. 1500 meters, sitting on leaf litter, 26.iv.2009, <i>leg.</i> P. Banar; four legs extracted for DNA, remaining appendages removed and mounted for SEM imaging.</p> <p> <i>Etymology.</i> The species epithet is referred to the collection locality near Parit Falls in the Cameron Highlands of West Malaysia.</p> <p> <i>Diagnosis.</i> Distinguished from congeners by the combination of the following characters: (1) dorsal surface of scutal areas I–IV with rings of dark pigmentation that do not cross the dorsal midline (<i>contra</i> solid patches in <i>P. distinctus</i>, <i>P. spiculosus, P. thaiensis</i>; rings crossing midline in <i>P. furculus</i>); (2) ventral pigmentation posterior to the genital operculum constituting three discontinuous patches, as a central arrowhead shape and lateral wings; (3) presence of two distinct lines of pigment stretching posteriorly from the ocularium (see Fig. 7a; <i>contra P. distinctus, P. spiculosus, P. suzukii, P. thaiensis</i>); (4) presence of two to three enlarged tubercles along the anterolateral margins of the fourth coxae (<i>contra P. spiculosus, P. suzukii, P. thaiensis</i>); (5) absence of enlarged tubercles on the anal plate (<i>contra P. thaiensis,</i> male <i>P. spiculosus</i>); (6) tarsal formula: 5: 10: 6: 6.</p> <p> <i>Description.</i> Female holotype, total length 2.57 mm, greatest width of prosoma 1.27 mm, greatest width of opisthosoma 1.76 mm; length-to-width ratio 1.46. Body pandurate (fiddle-shaped; Fig. 7a). Body light-brown in color with mottling, densely microgranulate surface microstructure. Eyes present on small ocularium with a single enlarged tubercle abutting the anterior margin of the carapace. Ocularium 0.34 mm long, 0.23 mm wide. Anterior margin of carapace with five pegs (two pairs on lateral margins with outermost longest, one at dorsal midline), typical of Assamiidae. Posterior margin of scutum with two prominent spines flanking midline and projecting posteriorly.</p> <p>Ventral prosomal complex (Fig. 7b) with coxae II and III meeting in midline, coxae I not so. Genital operculum subtriangular. Spiracles not apparent. Coxae IV highly enlarged (typical of Grassatores) with one enlarged tubercle along anterolateral margin and an enlarged tubercle laterally abutting trochanter IV projecting posteriorly. Cuticular projections span the gap between coxa IV and the anterior margin of sternite I, creating a bridge near the distal end of coxa IV. Free tergites smooth. Anal plate unarmed.</p> <p>Dorsal pigmentation with continuous band of dark pigment along lateral margin of the carapace; two solid patches of pigment flanking anterior-posterior axis immediately posterior to the ocularium and meeting in the midline; two arcuate patches of pigment toward posterior-lateral margin of the prosoma; prominent and complex arcs of pigmentation on scutal areas I–IV overlapping the midline; pegs at anterior margin of carapace indistinctly mottled; and spines on scutal area V pigmented. Ventral pigmentation prominently flanking ventral midline of opisthosomal segment II and the posterior margins of the leg IV coxae, creating slender and non-contiguous winged shapes with prominent anterior projection. Leg IV coxae also with lighter bands of pigment extending posteriorly to the junction of the leg IV trochanter and at the distal margin of coxae III. Pigmentation of opisthosoma present along ventral midline of sternites and complex wing-shaped pigmentation pattern on segment anterior to anal plate.</p> <p>Chelicerae (Fig. 8a) with prominent bulla on proximal article. Proximal article with denticulate granulation throughout basal territory. Article sparsely setose. Second article not incrassate, smooth, free of ornamentation. Several prominent setae along the length of the dorsal territory and along margin of distal article. Distal article with delicate dentition, free of ornamentation. Pedipalps (Fig. 8b, 8c) spoon-shaped and folded over chelicerae. Pedipalpal trochanter slender with two prominent setose tubercles at ventro-distal margin. Femur ventrally with a series of seven small, adjacent tubercles, lacking megaspines, restricted to proximal-most territory, and two additional disjunct tubercles midway along ventral surface. Femur dorsally with small setose tubercles toward distal end. Pedipalpal tibia with two large spines, one ventrally oriented at apex of prominent triangular projection, other dorso-laterally oriented. Pedipalpal tarsus with unornamented tarsal claw and four megaspines. Tarsal claw 0.27 mm long. Tarsus sparsely setose, with four megaspines ventro-distally, two flanking each side of the claw. Legs I–IV (Fig. 8d–g) slender, elongate, finely granulated, and with setiferous tubercles roughly arranged into rows along femora, patellae, tibiae, and metatarsi. Tarsal claws I–IV smooth, unmodified, double claws on legs III and IV (typical of Grassatores). Legs III and IV with tarsal process (Fig. 11c). Tarsal formula 5: 10: 6: 6.</p> <p>Male: Unknown.</p> <p> <i>Distribution.</i> Known only from the type locality (Fig. 12).</p>Published as part of <i>Klementz, Benjamin C. & Sharma, Prashant P., 2023, New species of Paktongius and convergent evolution of the gonyleptoid-like habitus in Southeast Asian Assamiidae (Opiliones: Laniatores), pp. 34-54 in Zootaxa 5389 (1)</i> on pages 44-47, DOI: 10.11646/zootaxa.5389.1.2, <a href="http://zenodo.org/record/10404551">http://zenodo.org/record/10404551</a>
Paktongius spiculosus Klementz & Sharma 2023, sp. nov.
<i>Paktongius spiculosus</i> sp. nov. <p>(Figs. 4–6, 11, 12; Tables 3–4)</p> <p> <i>Type material.</i> <i>Holotype.</i> ♀ (MHNG LT-10 /18) LAOS, Khammouan Province, Nam Kading NPA, Tad Mouang, ca. 1km northeast of Nahin, 18°13’13”N, 104°32’08”E, 270 m, disturbed primary forest, 26.ix.2010, <i>leg.</i> P. Schwendinger. L2-4 extracted for DNA; one of each appendage (L1-4; chelicera), both pedipalps dissected and mounted for SEM imaging.</p> <p> <i>Paratypes.</i> ♂ (UWZM Y.40171) Same collecting data as holotype. LAOS, Bolikhamxai Province, Phou Khao Khouay NPA, north of Ban Hadkhai, trail to Tad Xay, 18°27’05”N, 103°08’59”E, 300 m (secondary forest), 22.ix.2010, <i>leg.</i> P. Schwendinger. LT-10 /15. Genitalia and one of each appendage dissected and mounted for SEM imaging.</p> <p> <i>Etymology.</i> The species epithet is derived from the Latin for “spike” (<i>spiculo</i>) and highlights the prominent cluster of tubercles adorning the anal plate of the male, reminiscent of thorns or spikes.</p> <p> <i>Diagnosis.</i> Distinguished from congeners by the combination of the following characters:(1) dorsal pigmentation composed of solid dark patches that do not cross dorsal midline (<i>contra</i> rings in <i>P. suzukii, P. paritensis, P. furculus</i>; anterior-most patches crossing midline in <i>P. thaiensis</i>); (2) ventral pigmentation posterior to the genital operculum constituting subtriangular shape, without prominent “wings”; (3) absence of two distinct lines of pigment stretching posteriorly from the ocularium (<i>contra P. furculus, P. paritensis</i>); (4) presence of eight enlarged tubercles on the anal plate (males only); (5) absence of enlarged tubercles along the posterior margin of the scutum; (6) tarsal formula: 5: 9: 6: 6. Males additionally distinguished from congeners by the combination of three enlarged tubercles on the lateral margin of the leg IV femur (<i>contra P. suzukii</i>), and genitalia with five pairs of lateral setae (<i>contra P. suzukii</i>) and two dorso-apical cuticular projections (<i>contra P. thaiensis</i>).</p> <p> <i>Description.</i> Total length of female holotype (male paratype in parentheses) 2.56 mm (2.98 mm), greatest width of the prosoma 1.23 mm (1.28 mm), greatest width of the opisthosoma 2.20 mm (2.34 mm); length-to-width ratio 1.16 (1.27). Body campaniform with sub-rectangular posterior margin (Fig. 4). Body reddish brown in color with darker mottling (in alcohol, depending on incidence of light) in holotype, almost entirely with a dense microgranulate surface microstructure. Eyes present on small, unornamented ocularium that is set back from anterior margin of the carapace. Ocularium 0.24 mm (0.23 mm) long, 0.30 mm (0.32 mm) wide. Anterior margin of carapace with five pegs (two pairs on lateral margins, one at the dorsal midline), typical of Assamiidae. Scutal grooves of mesotergum indistinct. Scutal areas III–IV with pairs of small spines flanking the midline. Free tergites unarmed.</p> <p>Ventral prosoma complex (Fig. 4b, d) of male and female, with coxae II and III meeting in midline, coxae I not so. Genital operculum subtriangular in male, elliptical in female. Spiracles not apparent. Coxae IV of both male and female massively enlarged (for Grassatores).Anal plate armed with eight prominent tubercles in male, same number of small and blunt tubercles in female.</p> <p>Dorsal pigmentation of male absent (likely due to recent ecdysis event) (Fig. 4c, d). Dorsal pigmentation of female with continuous band of pigment along lateral margins of the carapace (Fig. 4a, b); mottled rings of dark pigmentation immediately posterior to ocularium; solid wing-shaped patches of pigmentation on scutal areas I–IV flanking the midline; and dark patches of pigmentation on both lateral pairs of pegs at anterior margin of the carapace. Ventral pigmentation of female indistinct except along ventral midline of opisthosomal segment II (between coxae IV), lateral margins of coxae IV, and flanking the midline at the posterior of coxae IV. Sternites posterior to opisthosomal segment II uniformly with darker pigmentation.</p> <p>Chelicerae (Figs. 5a, 6a) sexually monomorphic, with prominent bulla on proximal article. Proximal article with denticulate granulation basally and ventrally. Second article not incrassate, free of ornamentation, with dorsal and latero-distal margin bearing several setae. Distal article with delicate dentition, free of ornamentation. Pedipalps (Fig. 5b–c, 6b) spoon-shaped and folded over chelicerae. Pedipalpal trochanter slender with two prominent setose tubercles at ventro-distal margin. Pedipalpal femur ventrally with eight small tubercles, lacking megaspines and located in proximal half of femur; dorsally with small setose tubercles distally. Pedipalpal tibia with two ventrally oriented spines at the distal margin and one smaller spine at a ventro-lateral and proximal position. Spine length 0.23 mm (0.21 mm). Pedipalpal tarsus with four megaspines and unornamented tarsal claw. Legs I–IV (Fig. 5d–g, 6c–f) slender, elongate, finely granulated, with small and irregularly distributed setiferous tubercles on femora, patellae, tibiae, and metatarsi. Femur I of both male and female ventrally with prominent row of setose tubercles. Coxa II of both male and female with prominently projecting pegs, particularly at the posterior of trochanter II. Male femur IV ectally with four prominent setiferous tubercles (not present in female). Tarsal claws I–IV smooth, unmodified, double claws on legs III and IV (typical of Grassatores). Legs III and IV with tarsal process (Fig. 11b). Tarsal formula 5: 9: 6: 6.</p> <p>Male genitalia (Fig. 6g –h) typical of Assamiidae, with two cuticular dorsal projections distally; two pairs of apical setae; five pairs of setae on lateral margins of ventral plate; three pairs of setae on ventral plate.</p> <p> <i>Distribution.</i> Known from Khammouan and Bolikhamxai Provinces, Laos (Fig. 12).</p>Published as part of <i>Klementz, Benjamin C. & Sharma, Prashant P., 2023, New species of Paktongius and convergent evolution of the gonyleptoid-like habitus in Southeast Asian Assamiidae (Opiliones: Laniatores), pp. 34-54 in Zootaxa 5389 (1)</i> on pages 40-44, DOI: 10.11646/zootaxa.5389.1.2, <a href="http://zenodo.org/record/10404551">http://zenodo.org/record/10404551</a>
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