75,665 research outputs found
Casparson, J[ohann] W[ilhelm] C[hristian] G[ustav] an [Johann Jacob] Huber (1 Brief)
No full textCASPARSON, J[OHANN] W[ILHELM] C[HRISTIAN] G[USTAV] AN [JOHANN JACOB] HUBER (1 BRIEF)
Casparson, J[ohann] W[ilhelm] C[hristian] G[ustav] an [Johann Jacob] Huber (1 Brief) (Br5839)
Brief 5839 (Br5839
Measurement of the ratio of prompt χ c to J / ψ production in pp collisions at √s = 7 TeV
No full textThe 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
Politische Erinnerungen 1833 bis 1883
No full textJ. C. Kern ; herausgegeben unter Mitwirkung von Karl DuboisFrühere Signatur: "Bircher 3237" 990021275070205503_0004 Exemplar der ETH-BIBExlibrisetikette: "Aus der Bibliothek von Oberstdivisionär Eugen Bircher Aarau der Bibliothek der Eidgenössischen Technischen Hochschule geschenkt" 002125367_0001 Exemplar der ETH-BIB, Rar 15754Frühere Signatur: "Bircher 4313" 990021275070205503_0004 Exemplar der ETH-BI
Chibchea tunebo Huber 2000
No full textChibchea tunebo Huber, 2000 Figs 110–111, 127, 134–140, 1035 Chibchea tunebo Huber, 2000: 171, figs 652–655 (♂). Diagnosis Distinguished from similar congeners (C. merida Huber, 2000; C. thunbergae Huber sp. nov.; C. danielae Huber sp. nov.) by male chelicerae (Huber 2000: fig. 652; long hairs proximally, deep frontal invagination, short spine-like hairs distally) and by female internal genitalia (Figs 127, 137; Y-shaped anterior receptacle). Type material VENEZUELA – Táchira • ♂ holotype, AMNH, Pregonero, “2nd forest road at Camp Siberia”, 1280 m a.s.l. [approximately 7.893° N, 71.719° W], 10–13 Jul. 1989 (S. & J. Peck). New record VENEZUELA – Táchira • 3 ♂♂, 6 ♀♀, 2 juvs, ZFMK (Ar 21845), and 4 ♀♀, 4 juvs in pure ethanol, ZFMK (Ven20-120), SE Pregonero, forest near La Trampa (7.9236° N, 71.7152° W), 1300 m a.s.l., 10 Feb. 2020 (B.A. Huber, O. Villarreal M., Q. Arias C.). Assigned tentatively VENEZUELA – Mérida • 5 ♂♂, 1 ♀, ZFMK (Ar 21846), and 4 ♀♀, 1 juv. in pure ethanol, ZFMK (Ven20-135), forest above Caño Azul (8.8543° N, 71.3651° W), 280 m a.s.l., 13 Feb. 2020 (B.A. Huber, O. Villarreal M., Q. Arias C.) • 1 ♂, 3 ♀♀, 1 juv., ZFMK (Ar 21847), and 3 ♀♀ in pure ethanol, ZFMK (Ven20-109), Las Piedras, ‘site 2’ (8.9002° N, 70.6279° W), 1700 m a.s.l., degraded forest, 7 Feb. 2020 (B.A. Huber, O. Villarreal M., Q. Arias C.). Note We were not able to exactly locate the type locality “2 nd forest road at Camp Siberia”, but “Campamento Siberia” is at 3 km from our new collecting site, suggesting that the new site is within a few km from the type locality. Redescription of male (amendments; see Huber 2000) Measurements (male from near La Trampa): Total body length 2.4, carapace width 0.9. Distance PME– PME 80 µm; diameter PME 90 µm; distance PME–ALE 80 µm; distance AME–AME 15 µm; diameter AME 20 µm. Leg 1: 19.1 (4.4 +0.3+ 4.6+8.4+ 1.4), tibia 2: 3.0, tibia 3: 2.4, tibia 4: 3.2; tibia 1 L/d: 61. Pair of lateral distal patches of short modified hairs situated on low light brown humps. Retrolateral trichobothrium on tibia 1 at 10%; prolateral trichobothrium absent on tibia 1. Tibia 1 in three other newly collected males from near La Trampa: 4.2, 4.5, 4.7. Males from Caño Azul are slightly smaller (tibia 1 in five males: 3.6–4.2, mean 3.9) but appear otherwise indistinguishable from males from near La Trampa. They are assigned tentatively because of the accompanying females (see below). The male from Las Piedras has considerably shorter legs (tibia 1: 3.2), and the spines on the chelicerae are not divided into two patches on each side; the palps appear identical to males from La Trampa. Description of female Female in general very similar to male (Fig. 111). Epigynum simple, weakly curved transversal plate, without posterior plate (Fig. 134). Internal genitalia (Figs 127, 137–138) with pair of large oval pore plates, anterior transparent receptacle Y-shaped. Tibia 1 in six females: 3.2–3.6 (mean 3.4). Females from Caño Azul are slightly smaller (tibia 1 in five females: 2.7–3.0, mean 2.9) and have a slightly longer but narrower epigynal plate (Fig. 135; length/width: 0.22/0.34, versus 0.20/ 0.40 in females from near La Trampa). They are therefore assigned tentatively. The internal genitalia appear largely identical (large oval pore plates; Y-shaped anterior receptacle). Females from Las Piedras are slightly smaller (tibia 1 in six females: 2.7–3.0, mean 2.8) and the posterior epigynal margin is protruding rather than indented (Fig. 136); the internal genitalia (Figs 139–140) differ slightly in the shape of the pore plates (narrowing laterally) and in the shape of the receptacle (widened posteriorly rather than Y-shaped). They are therefore assigned tentatively. Distribution Known from three localities in the Venezuelan states Táchira and Mérida (Fig. 1035); however, specimens from Mérida are assigned tentatively. Natural history At all three new localities, the spiders were found in the leaf litter, in curved leaves that provided space for the small, weakly domed webs.Published as part of Huber, Bernhard A. & Villarreal, Osvaldo, 2020, On Venezuelan pholcid spiders (Araneae, Pholcidae), pp. 1-317 in European Journal of Taxonomy 718 on pages 44-46, DOI: 10.5852/ejt.2020.718.1101, http://zenodo.org/record/406957
Evidence for the decay B0→J/ψω and measurement of the relative branching fractions of meson decays to J/ψη and J/ψη′
No full textFirst evidence of the B 0 → J / ψ ω decay is found and the B s 0 → J / ψ η and B s 0 → J / ψ η ′ decays are studied using a dataset corresponding to an integrated luminosity of 1.0 fb -1 collected by the LHCb experiment in proton-proton collisions at a centre-of-mass energy of sqrt(s) = 7 TeV. The branching fractions of these decays are measured relative to that of the B 0 → J / ψ ρ 0 decay:frac(B (B 0 → J / ψ ω), B (B 0 → J / ψ ρ 0)) = 0.89 ± 0.19 (stat) - 0.13 + 0.07 (syst),frac(B (B s 0 → J / ψ η), B (B 0 → J / ψ ρ 0)) = 14.0 ± 1.2 (stat) - 1.5 + 1.1 (syst) - 1.0 + 1.1 (frac(f d, f s)),frac(B (B s 0 → J / ψ η ′), B (B 0 → J / ψ ρ 0)) = 12.7 ± 1.1 (stat) - 1.3 + 0.5 (syst) - 0.9 + 1.0 (frac(f d, f s)), where the last uncertainty is due to the knowledge of f d / f s, the ratio of b-quark hadronization factors that accounts for the different production rate of B 0 and B s 0 mesons. The ratio of the branching fractions of B s 0 → J / ψ η ′ and B s 0 → J / ψ η decays is measured to befrac(B (B s 0 → J / ψ η ′), B (B s 0 → J / ψ η)) = 0.90 ± 0.09 (stat) - 0.02 + 0.06 (syst)
Calapnita bankirai Huber, 2017, sp. nov.
No full textCalapnita bankirai sp. nov. Figs 18, 60–64 “ Calapnita phyllicola ” Deeleman-Reinhold, 1986 (misidentification): Deeleman-Reinhold 1986: 216 (part of paratypes). Huber 2011: 54 (part of paratypes and specimens from Balikpapan in ZFMK, see below). Diagnosis. Distinguished from most other species of phyllicola group (except C. bidayuh, C. phyllicola, C. semengoh) by shape of appendix (widely curved with two ventral tines; Fig. 62), by male palpal tarsal organ on cylindrical process of tarsus, by serrated edge of embolus, and by drop-shaped pore plates (Fig. 64); from closest known relatives (C. bidayuh, C. phyllicola, C. semengoh) by narrow tip of procursus (Fig. 61); from C. phyllicola also by presence of split hairs dorsally on procursus; from C. semengoh also by much shorter palpal segments and external female genitalia; from C. bidayuh also by absence of distal spine-like process on procursus. Females differ from C. phyllicola by absence of sclerotized transversal ridges on epigynum (Fig. 63) and by pore plates farther apart (Fig. 64); females of C. bidayuh and C. bankirai may not be distinguishable externally, but the pore plates in C. bankirai are slightly closer together (Fig. 64). Etymology. The species name is derived from the type locality; noun in apposition. Material examined. Holotype. INDONESIA-BORNEO: ♂, ZFMK (Ar 15994), East Kalimantan, Bukit Bankirai (1.029°S, 116.867°E), 100 m a.s.l., on green leaves in forest, 29.x.2009 (S. Sutono). Other material. INDONESIA-BORNEO: 4♂ 3♀, ZFMK (Ar 15995), same data as holotype; 1♀ 2 juvs in absolute ethanol, ZFMK (Ind 166), same data. Sepaku [~1.0°S, 116.9°E], 4♂ 2♀, RMNH (ARA 17803, 17386), misidentified paratypes of Calapnita phyllicola, 3 & 5.viii.1980 (2 vials) (P.R. & C.L. Deeleman). 1♂ 2♀, ZFMK (Ar 5333), Balikpapan [~1.25°S, 116.83°E], 20.vii.1982 (J. Murphy, 11873). MALAYSIA-BORNEO: 6♂ 4♀, ZFMK (Ar 15996–97), Sarawak, Niah Cave National Park, forest near headquarters (3.820°N, 113.763°E), 40 m a.s.l., night collecting, undersides of leaves, 28.vii.2014 (B.A. Huber, S.B. Huber); 1♂ 1♀, ZFMK (Ar 15998), Niah Cave National Park, forest near cave (3.814°N, 113.771°E), 40 m a.s.l., undersides of leaves, 28.vii.2014 (B.A. Huber). Description. Male (holotype) MEASUREMENTS. Total body length 5.2, carapace width 0.8. Leg 1: 35.1 (8.3 + 0.3 + 8.5 + 16.3 + 1.7), tibia 2: 5.9, tibia 3: 3.3, tibia 4: 5.2; tibia 1 L/d: 106. Distance PME-PME 240 µm, diameter PME 90 µm, distance PME- ALE ~30 µm; no trace of AME. COLOR. Entire animal mostly very pale whitish, legs slightly yellowish, patellae and tibia-metatarsus joints with short brown rings. BODY. Habitus as in Fig. 18; ocular area barely elevated, each triad on very low hump; carapace without median furrow; clypeus unmodified; sternum as wide as long (0.44), unmodified. CHELICERAE. As in C. phyllicola (cf. fig. 172 in Huber 2011), with pair of simple apophyses near lamellae and pair of indistinct lateral humps proximally; without modified hairs; without stridulatory ridges. PALPS. In general very similar to C. phyllicola (cf. figs 170–171 in Huber 2011); proximal segments apparently indistinguishable; procursus with two split hairs dorsally and with slender mostly weakly sclerotized tip (Figs 60– 61); appendix very slender, especially distally (Fig. 62). LEGS. Without spines and curved hairs; few vertical hairs; retrolateral trichobothrium on tibia 1 at 2%; prolateral trichobothrium absent on tibia 1, present on other tibiae; tarsus 1 pseudosegments very indistinct, only distally a few visible in dissecting microscope. Male (variation). Tibia 1 in 11 other males: 7.0–8.5 (mean 7.6). Female. In general similar to male; eye triads slightly closer together (distance PME-PME 210 µm). Tibia 1 in 9 females: 5.4–6.7 (mean 6.0). Epigynum very simple, very similar to C. bidayuh, almost entirely unsclerotized (Fig. 63); with simple short posterior ‘knob’; internal genitalia as in Fig. 64, with pair of membranous ‘sacs’. Natural history. At the type locality the spiders were found on the undersides of palm leaves. One male had an ectoparasitic mite on its prosoma (Fig. 18; cf. C. dinagat below). Distribution. Apparently widespread in Borneo, but known from only two localities (Fig. 282).Published as part of Bernhard A. Huber, 2017, Revision and cladistic analysis of the Southeast Asian leaf-dwelling spider genus Calapnita Simon (Araneae, Pholcidae), pp. 1-63 in Zootaxa 4219 (1) on pages 22-23, DOI: 10.5281/zenodo.27308
Shirley Huber
No full textShirley Huber is pictured her school year at Lapoint Elementary. She is the daughter of Elmer and Irva Fillerup Huber. She married Berlin C. Jensen. She was born April 12, 1930 and died August 10, 2012
Modisimus cuadro Huber & Fischer & Astrin 2010, SP. NOV.
No full text<i>MODISIMUS CUADRO</i> HUBER & FISCHER SP. NOV. <p>(Figs 56, 78, 99, 111, 112, 173–175, 200)</p> <p> <i>Type:</i> Male holotype from near La Toma (18°27.5 <i>′</i> N, 70°07.2 <i>′</i> W), San Cristóbal Prov., Dominican Republic;</p> <p>degraded forest at 70 m a.s.l., near ground, 7 November 2005 (B.A. Huber), in ZFMK (DR 5a).</p> <p> <i>Etymology:</i> The name is derived from the Spanish cuadro (square), and refers to the square-shaped epigynum; it is used as a noun in apposition.</p> <p> <i>Diagnosis:</i> Medium-sized species, distinguished from congeners by barely modified male chelicerae (Fig. 174; similar to <i>M. pelejil</i> sp. nov.), simple squareshaped epigynum (Fig. 56), and procursus shape (Figs 99, 173).</p> <p> <i>Male (holotype):</i> Total length, 2.7; carapace width, 1.4. Leg 1: 22.8 (5.9 + 0.4 + 6.1 + 8.8 + 1.6); tibia 2, 4.1; tibia 3, 3.1; tibia 4, 3.8. Tibia 1 L/d: 57. Habitus similar to <i>M. jima</i> sp. nov. (cf. Fig. 19), carapace pale ochre-yellow, with pair of light-brown marks on posterior half, and smaller indistinct pair in front of them; dark median line and wider dark median band visible through cuticle; ocular area laterally brown, clypeus with pair of brown stripes; sternum mostly light brown, whitish medially; legs light brown, tips of femora and tibiae lighter, very indistinct darker rings subdistally on femora and tibiae; abdomen bluish grey, densely covered with small black spots dorsally and laterally, with pale-bluish lines dorsally (medially) and laterally (two pairs). Ocular area elevated; thoracic furrow distinct. PME–PME, 135 Mm; PME diameter, 115 Mm; PME–ALE, 150 Mm; AME–AME, 20 Mm; AME diameter, 20 Mm. Sternum wider than long (0.8/0.6), unmodified. Chelicerae barely modified, with slightly stronger hairs proximally, and paler area with few hairs (Fig. 174). In general, palps very similar to <i>M. kiskeya</i> sp. nov. and <i>M. femoratus</i> (cf. Figs 124, 130), but procursus with distinctive mostly membranous projections distally (Figs 99, 173). Legs with short spines in single rows on femur 1 (~30 spines) and femur 2 (~20); many short vertical hairs on all femora; no curved hairs; retrolateral trichobothrium on tibia 1 at 11%; prolateral trichobothrium missing on tibia 1, present on other tibiae; tarsus 1 with ~25 pseudosegments.</p> <p> <i>Variation:</i> Tibia 1 in nine other males: 5.2–7.0 (mean 6.1). In some males, the brown marks on the carapace and/or the white-bluish lines on the abdomen are very indistinct; the male from near La Mula and two of the four males from Cuevas Pomier lack spines on femora 1 and 2, but have identical palps and chelicerae.</p> <p> <i>Female:</i> In general, similar to male; colour variation as in males. Tibia 1 in 12 females: 4.0–4.5 (mean 4.3). Epigynum, a simple brown plate (Fig. 56); dorsal view as in Figures 78 and 175, with anteriorly converging pore plates.</p> <p> <i>Distribution and habitat:</i> Known from several localities in the Dominican Republic (Fig. 200). This species typically occurs close to the ground, under logs and dead leaves, and in low vegetation.</p> <p> <i>Material examined:</i> Dominican Republic: San Cristóbal Prov., near Toma, 1♂, holotype above; same data, 4♂, 4♀ and four juveniles (ZFMK, DR 5); same data, 1♀, in pure ethanol (ZFMK, DR 100-3); Borbon, Cuevas Pomier, tropical deciduous forest, 200 m a.s.l., 13–28 July 1995 (S. & J. Peck), 1♂, #95-23 (AMNH); same data but 28 July–5 August 1995, #95-47, 3♂ (AMNH). Borbon, Cuevas Pomier, Cueva Puente, twilight zone, 13 July 1995 (S. & J. Peck), 1♀, #95-24 (AMNH); Borbon, Cuevas Pomier, C. Funeraria, 250 m a.s.l., 14 July 1995 (S. & J. Peck), 6♂, 2♀ and three juveniles, #95-28 (AMNH); Borbon, Cuevas Pomier, Cueva La Ligua, 13 July 1995 (S. & J. Peck), 1♂, #95-25 (part) (AMNH). Distrito Nacional, Santo Domingo, Jardín Botánico (18°29.7 <i>′</i> N, 69°57.2 <i>′</i> W), forest along brook, 50 m a.s.l., low vegetation, near ground, 27 November 2005 (B.A. Huber), 3♀ (ZFMK, DR 108); Jardín Botánico, under roof of shelter, 18–22 March 1984 (H. & L. Levi), 1♂ and 2♀ (MCZ). Peravia Prov., near Nizao (18°36.0 <i>′</i> N, 70°29.2 <i>′</i> W), degraded forest along river, 670 m a.s.l., 19 November 2005 (B.A. Huber), 1♂ (ZFMK, DR 78). Monte Plata Prov., near Monte Plata (18°48.7 <i>′</i> N, 69°47.1 <i>′</i> W), degraded forest along river, 60 m a.s.l., near ground, 21 November 2005 (B.A. Huber), 1♂, 2♀ (ZFMK, DR 92). San Pedro de Macorís Prov., near La Mula (18°30.2 <i>′</i> N, 69°36.7 <i>′</i> W), degraded forest at entrance to cave, 30 m a.s.l., 26 November 2005 (B.A. Huber), 1♂ and 2♀ (ZFMK, DR 107). La Romana Prov., forest at Rio Chavón (18°26.5 <i>′</i> N, 68°53.3 <i>′</i> W), 20 m a.s.l., 23 November 2005 (B.A. Huber), 2♀ and one juvenile (ZFMK, DR 101). La Vega Prov., 10 km north-east of Jarabacoa Raquet Club, 550 m a.s.l., mixed forest, 20 July–4 August 1995 (S. & J. Peck), 3♂ and one juvenile #95-37 (AMNH). María Trinidad Sánchez Prov., near La Entrada, forest above rocks at Santuario de La Virgen (19°34.9 <i>′</i> N, 69°54.0 <i>′</i> W), 15 m a.s.l., 12 November 2005 (B.A. Huber), 1♀ (ZFMK, DR 42).</p>Published as part of <i>Huber, Bernhard A., Fischer, Nadine & Astrin, Jonas J., 2010, High level of endemism in Haiti's last remaining forests: a revision of Modisimus (Araneae: Pholcidae) on Hispaniola, using morphology and molecules, pp. 244-299 in Zoological Journal of the Linnean Society 158 (2)</i> on pages 283-284, DOI: 10.1111/j.1096-3642.2009.00559.x, <a href="http://zenodo.org/record/5438272">http://zenodo.org/record/5438272</a>
Huber, Dolores C. (Birth, 1907-08-30)
No full textAddress: 3106 Warsaw Avenue3980/Pg.146/1907/F W/Cinti,Ohio/Ohio/Dr. Clarence J. BeekleyOriginal record filed in drawer labeled 'HUBER-HUHN'
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