1,762 research outputs found
Writers Talk Featuring Sonya Huber
No full textSonya Huber, 2004 graduate of OSU's MFA Creative Writing Program, currently an assistant professor at Georgia Southern University. Author of "The Backwards Research Guide for Writers," "Opa Nobody," and most recently "Cover Me: A Health Insurance Memoir."The media can be accessed here: http://streaming.osu.edu/knowledgebank/cstw12/WT_WCRS_11-08-10_SonyaHuber.mp3Ohio State University. Center for the Study and Teaching of Writin
Robust Linear and Support Vector Regression
No full textThe robust Huber M-estimator, a differentiable cost function that is quadratic for small errors and linear otherwise, is
modeled exactly, in the original primal space of the problem, by an easily solvable simple convex quadratic program for both linear and
nonlinear support vector estimators. Previous models were significantly more complex or formulated in the dual space and most
involved specialized numerical algorithms for solving the robust Huber linear estimator [3], [6], [12], [13], [14], [23], [28]. Numerical test
comparisons with these algorithms indicate the computational effectiveness of the new quadratic programming model for both linear
and nonlinear support vector problems. Results are shown on problems with as many as 20,000 data points, with considerably faster
running times on larger problems
Huber, Jack Burl (Birth, 1906-06-22)
No full textAddress: 826 State Avenue3250/Pg. 219/1906/M W/Indiana/Ky./Dr. C.J. LasanceOriginal record filed in drawer labeled 'HUBER-HUHN'
Mesabolivar amadoi Huber 2018, sp. n.
No full textMesabolivar amadoi sp. n. Figs 306–314 Diagnosis. Easily distinguished from most known congeners by armature of male chelicerae (Figs 310–311; two pairs of frontal apophyses), tip of procursus (Figs 308–309; distinctive shape of prolateral process), and shape of epigynum (Figs 312–313; anterior plate with large central whitish depression and pair of apophyses); from most similar known species (M. bonita) by apophyses on epigynum (absent in M. bonita) and by positions and sizes of male cheliceral apophyses (proximal apophyses smaller; distal apophyses in more proximal position). Etymology. Named for Jorge Amado (1912–2001), Brazilian writer, author of Gabriela, Cravo e Canela. Type material. BRAZIL: Bahia: ♂ holotype, 1♀ paratype, MNRJ (14319), 14♂ 10♀ paratypes, ZFMK (Ar 19147–48), Reserva Particular do Patrimônio Natural Serra Bonita (15°23.3’–23.4’S, 39°33.7’–34.0’W), ~ 750– 850 m a.s.l., 2–3.x.2011 (B.A. Huber, A. Pérez-González, M. Alves Dias). Other material examined. BRAZIL: Bahia: 1♂ 9♀ in pure ethanol, ZFMK (Br11-161), same data as types. Espírito Santo: 3♂ 16♀ 1 juv., ZFMK (Ar 19149–50), Reserva Biológica de Sooretama, ‘site 1’ (19°03.3’S, 40°08.8’W), ~ 90 m a.s.l., 27.ix.2011 (B.A. Huber, A. Pérez-González); 6♀ in pure ethanol, ZFMK (Br 11-126), same data. Description. Male (holotype) MEASUREMENTS. Total body length 3.3, carapace width 1.3. Distance PME-PME 130 µm, diameter PME 120 µm, distance PME-ALE 100 µm, distance AME-AME 30 µm, diameter AME 50 µm. Sternum width/length: 0.95/ 0.55. Leg 1: 38.7 (11.0 + 0.5 + 10.8 + 14.6 + 1.8), tibia 2: 7.6, tibia 3: 4.9, tibia 4: 7.3; tibia 1 L/d: 94. Femora 1–4 width (at half length): 0.14, 0.15, 0.22, 0.15. COLOR (in ethanol). Prosoma and legs light brown, carapace with large dark median mark, clypeus not darker; tips of femora and tibiae lighter yellowish, legs without dark rings; abdomen greenish gray, dorsally and laterally densely covered with dark marks, ventrally with light brown area in front of gonopore. BODY. Habitus as in putative close relatives (M. bonita, M. pau; cf. Huber 2015: figs 12–13); ocular area raised; carapace with distinct median furrow; clypeus unmodified; sternum unmodified. CHELICERAE. With two pairs of frontal apophyses (Figs 310–311), both pointed in lateral view, distal pair rounded in frontal view. PALPS. As in Figs 306–307; apparently indistinguishable from M. bonita (direct comparison with M. bonita paratype); even details of procursus tip (Figs 308–309) apparently identical. LEGS. Without spines, without curved hairs, few vertical hairs; retrolateral trichobothrium on tibia 1 at 2%; prolateral trichobothrium present on tibia 1; tarsus 1 with>30 pseudosegments, distally fairly distinct. Male (variation). Tibia 1 in 15 other males: 9.4–11.2 (mean 10.2). Female. In general similar to male. Tibia 1 in 25 females: 5.9–8.5 (mean 7.0). Epigynum as in Figs 312–313; anterior plate with large central whitish depression bordered by posterior ridge and pair of apophyses near posterior margin; simple posterior plate. Internal genitalia as in Fig. 314, with pair of large pore-plates in tent-shaped lateral position, converging anteriorly. Natural history. The spiders were found in domed webs built in sheltered spaces close to the ground. Distribution. Known from two localities in Bahia and Espírito Santo states (Brazil) (Fig. 734).Published as part of Huber, Bernhard A., 2018, The South American spider genera Mesabolivar and Carapoia (Araneae, Pholcidae): new species and a framework for redrawing generic limits, pp. 1-178 in Zootaxa 4395 (1) on pages 76-79, DOI: 10.11646/zootaxa.4395.1.1, http://zenodo.org/record/120251
Mesabolivar claricae Huber 2018, sp. n.
No full textMesabolivar claricae sp. n. Figs 233–240, 251–252 Diagnosis. Distinguished from most known congeners by armature of male chelicerae (Figs 238–239; one pair of frontal apophyses near median line), shape of procursus (Figs 233–235; widely curved, distinctive distal structures, without prolateral apophysis), and shape of epigynum (Figs 236–237, 251; trapezoidal anterior plate with pair of apophyses and median pocket); from the very similar to M. cyaneomaculatus by shorter and wider procursus with different distal elements (compare Figs 227–229 and 233–235), and by smaller epigynum without anterior pair of low humps (compare Figs 230–232 and 236–237). Etymology. Named for Clarice Lispector (1920–1977), Brazilian writer, daughter of Russian-Jewish immigrants, author of Perto do coração selvagem. Type material. BRAZIL: Rio de Janeiro: ♂ holotype, 1♀ paratype, MNRJ (14315), 6♂ 19♀ paratypes, ZFMK (Ar 19082–83), Santa Maria Madalena, forest fragment (21°58.9’–59.1’S, 41°57.2’–57.6’W), 480–590 m a.s.l., 30.ix.–1.x.2010 (B.A. Huber, A. Pérez-González). Other material examined. BRAZIL: Rio de Janeiro: 4♀ in pure ethanol, ZFMK (Br 10-78), same data as types. 3♂ 4♀, ZFMK (Ar 19084), Cachoeiras de Macacu, Reserva Ecológica de Guapiaçú (22°24.4’–25.3’S, 42°44.2’–44.3’W), 140–280 m a.s.l., 23.ix.2009 (B.A. Huber, A. Giupponi); 1♂ in pure ethanol, ZFMK (Br 09- 101), same data but 23–24.ix.2009 (B.A. Huber); 2♂, ZFMK (Ar 19085), same data but 25.ix.2009 (B.A. Huber); 2♂ 2♀, ZFMK (Ar 19086), same locality at 22°24.3’S, 42°44.1’W, ~ 300–400 m a.s.l., 24.ix.2009 (B.A. Huber, A. Giupponi). Description. Male (holotype) MEASUREMENTS. Total body length 3.7, carapace width 1.35. Distance PME-PME 110 µm, diameter PME 150 µm, distance PME-ALE 100 µm, distance AME-AME 40 µm, diameter AME 45 µm. Sternum width/length: 1.0/ 0.65. Leg 1: 57.6 (13.7 + 0.5 + 13.5 + 26.8 + 3.1), tibia 2: 8.7, tibia 3: 5.5, tibia 4: 8.3; tibia 1 L/d: 104. Femora 1– 4 width (at half length): 0.17, 0.23, 0.23, 0.17. COLOR (in ethanol). Carapace ochre-orange with large brown median mark including posterior part of ocular area, with pair of light marks laterally behind ocular area; sternum orange-brown; legs brown, tips of femora and tibiae lighter yellowish, without dark rings; abdomen greenish gray, dorsally and laterally densely covered with dark marks, ventrally with orange-brown area in front of gonopore, very indistinct plate in front of spinnerets. BODY. Habitus very similar to M. cyaneomaculatus (cf. Figs 148–149); ocular area raised; carapace with distinct median furrow; clypeus unmodified; sternum unmodified. CHELICERAE. With one pair of frontal apophyses close to median line (Figs 238–239). PALPS. In general very similar to M. cyaneomaculatus (cf. Huber 2000: figs 813, 816), proximal segments apparently identical in shape but slightly smaller (see Variation below); procursus distal part (after bend) clearly shorter and wider, with different distal elements (Figs 233–235); bulbal process in general very similar to M. cyaneomaculatus but clearly shorter (length about 0.4 vs. 0.6). LEGS. Without spines, without curved hairs, few vertical hairs; retrolateral trichobothrium on tibia 1 at 2%; prolateral trichobothrium present on tibia 1; tarsus 1 with>40 pseudosegments, distally fairly distinct. Male (variation). Tibia 1 in nine other males: 12.4–14.1 (mean 13.2). Palpal femur length 0.60–0.62 (vs. 0.67– 0.73 in M. cyaneomaculatus). Female. In general similar to male but all leg femora approximately same width. Tibia 1 in 14 females: 8.7– 10.3 (mean 9.5). Epigynum as in Figs 236–237, 251; anterior plate trapezoidal, with pair of short processes (slightly variable in size even within localities) and median pocket near posterior margin; simple posterior plate. Internal genitalia as in Figs 240, 252, with V-shaped (or U-shaped) sclerite and pair of large pore-plates in tentshaped lateral position, converging anteriorly. Distribution. Known from two localities in Rio de Janeiro state (Brazil) (Fig. 728).Published as part of Huber, Bernhard A., 2018, The South American spider genera Mesabolivar and Carapoia (Araneae, Pholcidae): new species and a framework for redrawing generic limits, pp. 1-178 in Zootaxa 4395 (1) on pages 62-63, DOI: 10.11646/zootaxa.4395.1.1, http://zenodo.org/record/120251
Huber Family history Records
No full textTyped copy of the history of his biological parents and his adoptive parents. Parents were Philip J. Huber and Rose Engel. His father emigrated from Odessa, Russia in 1907, worked on various farms in Wells County, N.D., and began farming on his own 1921. First wife died in 1929, Harold's mother was from Nebraska, she had moved to N.D. in 1931. Her maiden name was Engel. John "Jack" Miller, born in Cornwall, Ontario, immigrated to Buffalo, N.D. 1910. Owned a drugstore in Balfour, N.D.; married Martha E. Sampson, Minot, N.D., circa 1918. They moved to Harvey, N.D. Miller died in 1951
Investigating the role of the nuclear receptor NR4A1 in T cell activation and T cell glucose metabolism
No full textAuthor: Nina Huber, BSc.Zusammenfassung in deutscher SpracheMasterarbeit University of Innsbruck 201
Investigating the role of the nuclear receptor NR4A1 in T cell activation and T cell glucose metabolism
No full textAuthor: Nina Huber, BSc.Zusammenfassung in deutscher SpracheMasterarbeit University of Innsbruck 201
Investigating the role of the nuclear receptor NR4A1 in T cell activation and T cell glucose metabolism
No full textAuthor: Nina Huber, BSc.Zusammenfassung in deutscher SpracheMasterarbeit University of Innsbruck 201
Comparing the distortionary effects of alternative in-kind intergovernmental transfers
No full textThis paper compares the distortions associated with alternative inter-governmental allocation rules when a central authority provides inputs for the provision of social services by local governments, and when local governments differ in their needs. Under a quantity-based mechanism, the input choices of high-need localities will tend to be distorted downwards. In order to convince the center of their higher needs, these communities signal their status by spending too little. However, under an expenditure-based mechanism the direction of distortion of the input choices of high-need localities depends on the price elasticity of demand for the local input. When demand is inelastic (elastic), in order to signal their high needs, high-need localities spend too much (little) on local inputs.Inter-governmental transfers, matching grants
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