4,665 research outputs found
Hemigrammus changae Ota & Lima & Hidalgo 2019, new species
No full textHemigrammus changae, new species (Figs. 1–3) Hemigrammus cf. lunatus (not Durbin): Mirande, 2018: 9 (phylogenetic relationships; based on a specimen from lot MUSM 3927). Holotype: MUSM 663836, 29.9 mm SL, Peru, Departamento Madre de Dios, Puerto Maldonado, Aguajal Cicra, Aguajal Pozo Minero, 12 o 33'48"S 70 o 07'03"W, 9 Dec 2003, M.H. Hidalgo. Paratypes: All from Peru. Departamento Madre de Dios: MUSM 21644, 34, 1 c&s, 22.3–28.7 mm SL; CAS 246141, 10, 23.1 – 27.6 mm SL; FMNH 138666, 10, 24.1 – 27.8 mm SL; MCZ 173322, 8, 24.1 – 27.1 mm SL; ZUEC 17027, 10, 23.5 – 26.7 mm SL; same data as holotype. MUSM 3927, 151, 3 c&s, 16.0–24.0 mm SL; ZUEC 17029, 7, 3 c&s, 19.1–22.3 mm SL, Zona Reservada Tambopata Candamo, La Colpa, cocha tributary of río Tambopata, ca. 12°55'S 69°15'W, 22 Aug 1992, F. Chang & J. Icochea. MUSM 5600, 14, 21.0– 26.4 mm SL, Zona Reservada Tambopata Candamo, Las Piedras, quebrada 2 km from lago Sandoval, ca. 12°36'S 69°03'W, 23 Jan 1990, H. Ortega, F. Chang & F. Rodriguez. MUSM 8563, 9, 19.5 – 23.8 mm SL, Puerto Maldonado, La Cachuela, 12°34'45"S 69°11'13"W, 12 March 1995, H. Ortega. MUSM 21701, 18, 10.8 – 26.3 mm SL, Puerto Maldonado, Aguajal Satélite, Aguajal Aguas Negras, 12°39'26"S 69°26'29"W, 22 Jan 2004, M.H. Hidalgo. MUSM 21823, 58, 10.2 – 27.9 mm SL, Puerto Maldonado, Aguajal Aguas Negras, Aguajal Pozo Minero, 12 o 38'10"S 69 o 25'36"W, 21 Jan 2004, M.H. Hidalgo. INPA 57938, 10, 4 c&s, 23.6–28.0 mm SL; MUSM 21992, 126, 10.5 – 29.3 mm SL; MUSM 22018, 83, 12.2 – 30.4 mm SL, Puerto Maldonado, Aguajal Este, lower río Madre de Dios, San Francisco, 12 o 28'11"S 68 o 56'04"W, 20–21 Feb 2004, M.H. Hidalgo. MUSM 22055, 27, 16.0– 30.3 mm SL; MUSM 22068, 149, 10.6 – 29.6 mm SL; ZUEC 17028, 4, 19.1 – 29.7 mm SL, Puerto Maldonado, Puerto Pardo, Aguajal Tripa, lower río Madre de Dios, 12°29'34''S 68°57'31''W, 22–23 Feb 2004, M.H. Hidalgo. MUSM 22135, 40, 9.8 – 27.3 mm SL, Puerto Maldonado, San Francisco, Aguajal Trigoso, lower río Madre de Dios, 12 o 27'58"S 68 o 52'53"W, 28 Feb 2004, M.H. Hidalgo. MUSM 22040, 58, 13.5 – 25.3 mm SL, Puerto Maldonado, San Francisco, Aguajal Pozo Paiche, lower río Madre de Dios, 12 o 29'05"S 68 o 57'09"W, 22 Feb 2004, M.H. Hidalgo. Departamento Puno: MUSM 52037, 1, 21.9 mm SL, Cocha Wiener, río Heath, 13 o 19'11"S 68 o 52'32"W, 18 Jun 2013, J. Chuctaya et al. Non-types: Peru, Departamento Madre de Dios: MUSM 2919, 24, 14.8 – 23.5 mm SL, Zona Reservada Tambopata Candamo, La Colpa, Quebrada Grande, tributary of río Tambopata, ca. 12°55'S 69°15'W; 31 Aug 1992, F. Chang. MUSM 22094, 10, 10.3 – 13.5 mm SL, Puerto Maldonado, Aguajal Oeste, tributary of río Madre de Dios, 12°28'40"S 68°58'18"W, 25 Feb 2004, M.H. Hidalgo. MUSM 22112, 25, 14.1 – 19.1 mm SL, Puerto Maldonado, Aguajal Gamitana, 12°27'08"S 69°00'32"W, 26 Feb 2004, M.H. Hidalgo. MUSM 25387, 41, 16.5 – 32.1 mm SL, Tahuamanu, río Manuripe, Cocha Macana, ca. 11°49'S 69°32'W, 12 Jul 2004, M.H. Hidalgo et al. MUSM 52701, 1, 20.4 mm SL, Mavila, cocha tributary of río Manuripe, 11°55'37"S 69°06'51"W, 23 Jul 2003, M.H. Hidalgo et al. MUSM 52699, 1, 25.5 mm SL, Manu, Quebrada Carachama, tributary of río Amiguillos, tributary of río Los Amigos, 12°26'40"S 70°15'43"W, 19 Jun 2004, M.H. Hidalgo et al. Bolivia, Departamento Beni: USNM 305661, 7, 20.9 – 22.3 mm SL, Arroyo Aguas Negras, tributary of río Curiraba, 3 km above mouth, 12 km N El Porvenir Biological Station, 40 km E San Borja, río Mamoré basin, ca. 14°55'S 66°17'W, 1 Sep 1987, W.C. Starnes & T. Munroe. MHNG 2228.086, 8, 22.0–25.0 mm SL, tributary of río Chapare, 50 km from confluence with río Mamoré, ca. 15°22'S 65°2'W, 21 Jun 1982, L. Lauzanne & G. Loubens. Departamento Cochabamba: MHNG 2180.097, 5, 23.6 – 27.8 mm SL, río Chapare, "Hoffman Lagune" below Todos Santos, ca. 16°50'S 65°17'W, 7 Oct 1966, K.H. Lüling. Departamento Santa Cruz: MHNG 2228.075, 2, 11.3 – 19.5 mm SL, río Yapacani, near Yapacani, tributary of río Grande, ca. 17°23'S 63°51'W, Sep 1983, W. Staeck & H. Linke. MHNG 2270.056, 2, 21.5 – 23.8 mm SL, same locality and collectors as MHNG 2228.075, 19 March 1985. Diagnosis. Hemigrammus changae differs from most congeners except from H. barrigonae, H. lunatus, H. machadoi, and H. ulreyi by possessing a wide dark horizontal stripe across the eye (vs. eye stripe absent or, when present, vertical). The new species can be additionally distinguished from all congeners, with the exception of Hemigrammus barrigonae, H. boesemani, H. geisleri, H. lunatus, H. machadoi, H. mimus, and H. ulreyi, by presenting a well-defined narrow dark stripe at the basis of the anal fin (vs. absence of dark stripe at the basis of anal fin). It can be distinguished from H. boesemani, H. geisleri, and H. mimus by lacking a blotch on caudal peduncle or any distinct patch of pigmentation on caudal fin (vs. a dark blotch on caudal peduncle or at the base of caudal fin present). Hemigrammus changae can be additionally diagnosed from Hemigrammus geisleri and H. mimus by lacking a pseudotympanum (vs. presence of a conspicuous pseudotympanum). The new species can be diagnosed from H. barrigonae, H. lunatus, and H. machadoi by presenting an oval, horizontally elongated humeral blotch (vs. a diffuse, vertically-elongated humeral blotch in H. barrigonae; a small rounded humeral blotch in H. lunatus; a rectangular, vertically-elongated blotch in H. machadoi). Hemigrammus changae can be distinguished from H. ulreyi by the absence of a patch of dark pigmentation on the basis of anteriormost dorsal-fin rays (vs. presence of a patch of dark pigmentation on the basis of anteriormost dorsal-fin rays). The new species can be additionaly distinguished from H. ulreyi, as well as from H. barrigonae, by lacking a conspicuous midlateral stripe (vs. presence of a conspicuous midlateral stripe). Hemigrammus changae can be additionally diagnosed from H. machadoi by presenting 6–7 gill-rakers on upper branch and 10–12, mode 12, on lower (vs. 4–5, and 9–10, mode 9, respectively), and more vertebrae (34–35 vs. 32–33), and from H. lunatus by presenting a higher number of cusps on maxillary largest tooth (5 vs. 1–3). Description. Morphometric data summarized in Table 1. Body compressed, moderately high; greatest body depth anterior to dorsal-fin origin. Dorsal profile of head slightly convex from tip of snout to anterior naris; straight to gently concave from latter point to tip of supraoccipital spine. Dorsal profile of body slightly to moderately convex from tip of supraoccipital spine to dorsal-fin origin; posteroventraly slanted from latter point to adipose-fin origin and slightly concave along caudal peduncle. Ventral profile of body convex from tip of dentary to anal-fin origin, posteroventraly slanted along anal-fin base. Ventral profile of caudal peduncle slightly to moderately concave. TABLE I. Morphometric data of Hemigrammus changae, new species. N = Number of specimens, and SD = standard deviation; all including the holotype. Mouth terminal; jaws equal, isognathous. Maxillary slightly curved, distal tip extending beyond vertical through anterior margin of eye. Premaxillary teeth in two rows, outer row composed by 3*(40) or 4(18) tri- to pentacuspid teeth, central cusp longer; inner row with 5*(78) penta- to heptacuspid teeth teeth, central cusp longer. Maxillary with 2(8) to 3(1) tri- to pentacuspid teeth along anteroventral margin, anteriormost tooth broader and always pentacuspid. Dentary with 9(1), 10(1), 11(3), 12(2), 13(1), or 15(1) teeth, anteriomost four teeth larger than remaining, with 5–7 cusps, central cusp longer, then gradually decreasing in size, 1–2 pentacuspid teeth, and remaining 4–9 tri- or unicuspid, small teeth (Fig. 2). Scales cycloid. Lateral line incomplete, slightly curved ventrally, with 6(7), 7(9), 8*(15), 9(13), 10(8), or 11(2) pored scales; longitudinal series including perforated scales 29(1), 30(1), 31*(5), 32(8), 33(19), 34(13), or 35(7). Scales rows between dorsal-fin origin and lateral line 5*(54); 3*(23) or 4(31) between lateral line and pelvic-fin insertion. Predorsal scales 9(4), 10*(32), or 11(18). Anal sheath along anal-fin base with 5 or 6 scales in a single row, covering base of first unbranched to fourth branched anal-fin rays. Circumpeduncular scales 10(41), 11*(7) or 12(6). Caudal-fin scales covering approximately basal third of upper and lower caudal-fin lobes margins, gradually decreasing in size. Dorsal-fin rays ii,9*(54), first unbranched ray nearly one-third of second unbranched ray length; small ossification anterior to first unbranched ray present in all six c&s specimens examined. Dorsal-fin distal margin straight. Dorsal-fin origin at midbody or slightly behind this point; base of posteriormost dorsal-fin ray slightly behind vertical through anal-fin origin. Insertion of first dorsal-fin pterygiophore posterior to neural spine of 9th(6) vertebra. Adipose fin present. Pectoral-fin rays i,10*(52) or 11(1). Pelvic-fin rays i,7*(53), pelvic-fin origin ahead of vertical through dorsal-fin origin; tip of longest ray exceeding anal-fin origin. Anal-fin rays iv, 20(4), 21(4), 22*(11), 23(17), 24(15), or 25(2); last unbranched ray to fifth branched ray longest, remaining rays gradually decreasing in size to anal-fin terminus, forming a conspicuous anterior fin lobe. Last anal-fin pterygiophore insertion behind hemal spine of 14(1) or 15(5) caudal vertebrae. Caudal fin forked, lobes slightly pointed, equal in size. Principal caudal-fin rays i,17,i*(45); dorsal procurrent caudal-fin rays 10(4) or 11(3); ventral procurrent caudal-fin rays 7(2) or 8(5). Vertebrae 33(2) or 34(5). Supraneurals 4(6) or 5(1). Branchiostegal rays 4(5). Upper branch of gill-rakers 6(4) or 7(1), lower branch 10(9), 11(18) or 12(20). Color in alcohol. Overall body ground coloration light tan. Anterior portion of lower jaw, maxillary, first infraorbital, snout and dorsal portion of head with intense concentration of small dark chromatophores, imparting an overall darker color. Gular region and infraorbitals clearer; third infraorbital and opercle series silvery in specimens retaining guanine pigmentation. Opercle and infraorbitals with scattered, relatively large dark chromatophores. Eye with a broad dark longitudinal midlateral stripe (not discernible in specimens preserved for a long period in formalin). Longitudinal dark stripe along midline of body present, very faint and narrow, originating after small concentration of dark chromatophores posterior to humeral blotch and extending up to approximately vertical through middle of caudal peduncle or slightly behind this point. Scales from dorsal region of body, in some specimens almost all scales on body (Fig. 1C), posteriorly bordered with dark chromatophores, forming a subtle reticulate pattern. Dark humeral blotch conspicuous, roughly oval, extending horizontally from second through fifth lateral-line scales, and vertically from lateral line to one row above lateral line to one scale row above it. Dark chromatophores below midlateral line arranged along margins of hypaxial muscles bundles from area above anal fin to caudal peduncle. Narrow, very conspicuous dark stripe along anal-fin basis. Fins hyaline, with scattered dark chromatophores, more numerous on dorsal- and anal-fins. Color in life. Based on pictures of living specimens (not preserved) collected at the río Madre de Dios basin. Head and abdominal region silvery. Body olive-grey, translucent. A narrow midlateral iridescent green stripe, running from humeral blotch to caudal peduncle. Fins hyaline, with a yellow hue. Sexual dimorphism. Anal-fin hooks were observed in males of Hemigrammus changae collected in August (MUSM 3927, 1, 23.7 mm SL), December (ZUEC 17027, 4, 22.2–23.6 mm SL; FMNH 138666, 2, 24.0– 24.5 mm SL; MCZ 173322, 1, 23.5 mm SL; CAS 246141, 3, 23.5–24.0 mm SL), or February (INPA 57938, 2, 23.0– 23.1 mm SL; MUSM 22018, 5, 23.3–25.0 mm SL; and MUSM 22040, 2, 23.0– 23.3 mm SL). Anal fin with 7–11 tiny hooks, arranged over the last unbranched ray and anteriormost 3–5 branched fin rays, one pair per ray segment. Pelvic-fin hooks were not observed in any specimens. Larger specimens (equal or above 26.0 mm SL) always lack anal-fin hooks and presumably are all females, which consequently are inferred to grow larger than males (the largest specimen examined with anal-fin hooks has 25.0 mm SL, MUSM 22018). Distribution. Hemigrammus changae is so far known from the río Madre de Dios and from the río Mamoré basins, upper río Madeira basin, in southeastern Peru and Bolivia (Fig. 3). The new species is apparently endemic from the freshwater ecorregion Mamoré-Madre de Dios Piedmont (Abell et al., 2008). Ecological notes. Most localities from where Hemigrammus changae is known are slow-flowing streams at "aguajales" (wetlands dominated by Mauritia flexuosa palms). These streams typically possess black water, a large amount of decayed organic matter, and are typically shallow. The type locality was a former a gold mining area that is in the process of recovery due to the implantation of a private conservation concession. Hemigrammus changae is also recorded from oxbow lakes and, in Bolivia, from lakes and streams at the llanos (seasonally flooded savannahs). The species is sympatric, and in some localities syntopic with Hemigrammus lunatus, but the latter species is more commonly found in floodplain lakes from white water rivers, a type of habitat where H. changae is apparently uncommon. Etymology. The specific name honors the late Fonchii Ingrid Chang Matzunaga, a Peruvian ichthyologist, from Chinese and Japanese ancestry, born on April 30, 1963 in Lima, Peru, who drowned when the boat she was in capsized on August 15, 1999, during an expedition at río Pastaza, Peru. We dedicate to her the new species as a tribute for her considerable contribution in surveying the fishes of her native country, in the relatively little time she was active, which included collecting part of the material herein examined of H. changae. A genitive noun.Published as part of Ota, Rafaela P., Lima, Flávio C. T. & Hidalgo, Max H., 2019, Description of a new Hemigrammus Gill (Characiformes: Characidae) from the río Madeira basin in Peru and Bolivia, pp. 335-347 in Zootaxa 4577 (2) on pages 336-341, DOI: 10.11646/zootaxa.4577.2.6, http://zenodo.org/record/262973
Romances contra Hidalgo y Marroquín de Francisco Estrada y Terán
No full textThis essay presents two romances of historical character, writings in favour of the State and the Spanish Crown and in opposition to the insurgent movement; in these texts one attacks, especially, the priest Hidalgo and the bullfighter Agustin Morroquin, who was nominated a deputy by the own Hidalgo. The romances were printed in the moment itself in which there were provoked the events of the War of Independence and appeared without author, my search has made possible that now we know the one who was his author: the Licentiate Francisco Estrada y Teran. The essay does the times of introduction and, at the same time, there are checked his literary and historical characteristics; the romances are reproduced, with spelling and punctuation modernized, to the philologic use and with a device of notes of character historically. There treats about the first two of the literary manifestations novohispanas of thematic counterinsurgent and they recover about the celebrations of the bicentenary of the beginning of the heroic Mexican exploit.Este ensayo presenta dos romances de carácter histórico escritos en favor del Estado y la Corona española y en contra del movimiento insurgente. En estos textos se ataca en particular al cura Hidalgo y al torero Agustín Morroquín, quien fue nombrado lugarteniente por el propio Hidalgo. Los romances fueron impresos en el momento mismo en que se suscitaban los acontecimientos de la guerra de Independencia y aparecieron sin firma, mi búsqueda ha hecho posible que ahora sepamos quién fue su autor: el licenciado Francisco Estrada y Terán. El ensayo hace las veces de introducción, y al mismo tiempo, se revisan sus características literarias e históricas; se reproducen los romances, con ortografía y puntuación modernizadas al uso filológico y con un aparato de notas de carácter histórico. Se trata de dos de las primeras manifestaciones literarias novohispanas de temática contrainsurgente y se recuperan a propósito de las celebraciones del bicentenario del inicio de la heroica gesta mexicana
CR1 Knops blood group alleles are not associated with severe malaria in the Gambia
No full textThe Knops blood group antigen erythrocyte polymorphisms have been associated with reduced falciparum malaria-based in vitro rosette formation (putative malaria virulence factor). Having previously identified single-nucleotide polymorphisms (SNPs) in the human complement receptor 1 (CR1/CD35) gene underlying the Knops antithetical antigens Sl1/Sl2 and McC(a)/McC(b), we have now performed genotype comparisons to test associations between these two molecular variants and severe malaria in West African children living in the Gambia. While SNPs associated with Sl:2 and McC(b+) were equally distributed among malaria-infected children with severe malaria and control children not infected with malaria parasites, high allele frequencies for Sl 2 (0.800, 1,365/1,706) and McC(b) (0.385, 658/1706) were observed. Further, when compared to the Sl 1/McC(a) allele observed in all populations, the African Sl 2/McC(b) allele appears to have evolved as a result of positive selection (modified Nei-Gojobori test Ka-Ks/s.e.=1.77, P-valu
Desde la portería del Liceo Hidalgo. Ángel de Campo Micrós, entre el nacionalismo y el modernismo
No full textEste artículo aporta al estudio de la crítica de Hilarión Frías y Soto (El Portero del Liceo Hidalgo) sobre la obra de Ángel de Campo Micrós. Analiza la narrativa de éste en la prensa capitalina de fin del siglo XIX, pasando por su filiación al nacionalismo y su necesidad de adaptarse a la nueva estética decadentista; todo esto bajo la luz de algunos conceptos de la sociología literaria de Pierre Bourdieu. A partir de las observaciones que Ángel Rama hace sobre el régimen porfiriano en nuestra capital en La ciudad letrada, también se estudia la obra de Micrós en la Revista Azul, poniendo de relieve su eclecticismo nacionalista y modernista
Quantum and its irreducible representations
No full textWe define for real a unital -algebra
quantizing the universal enveloping
-algebra of . The -algebra
is realized as a -subalgebra of the
Drinfeld double of and its dual Hopf -algebra
, generated by the equatorial Podle\'s sphere coideal
-subalgebra of and
its associated orthogonal coideal -subalgebra . We then classify all the irreducible
-representations of .Comment: 22 pages; author accepted manuscrip
Diseño de la imagen corporativa de una empresa del sector del metal RUAMPA SL
No full text[ES] Rediseño de la imagen corporativa, y la creación del manual de identidad de
una Empresa Familiar del sector del metal, de cuatro trabajadores, que se dedica al rectificado y lapeado de
diversidad de piezas metálicas.Hidalgo Hernández, Á. (2012). Diseño de la imagen corporativa de una empresa del sector del metal RUAMPA SL. https://riunet.upv.es/handle/10251/182164Archivo delegad
On the sheaf-theoretic SL(2, C) Casson–Lin invariant
No full textWe prove that the (τ-weighted, sheaf-theoretic) SL(2, C) Casson–Lin invariant introduced by Manolescu and the first author is generically independent of the parameter τ and additive under connected sums of knots in integral homology 3-spheres. This addresses two questions asked by Manolescu and the first author. Our arguments involve a mix of topology and algebraic geometry, and rely crucially on the fact that the SL(2, C) Casson–Lin invariant admits an alternative interpretation via the theory of Behrend functions.</p
Candidatus Rhetoricae (or Novus Candidatus).
No full textThis little book is a find whatever it finally turns out to be! For now it seems to be a Jesuit collegium text in rhetoric following the Progymnasmata of Aphthonius. If one works from the back of the book, there is an apparently independent 48-page work, Angelus Pacis by Nicolas Caussini (Latinized name), S.J. The rest of the book seems to be a commentary on or presentation of Aphthonius' Progymnasmata in 3 parts covering 435 pages, followed by a T of C and an AI, which is often one page off. Pars II is titled Rhetoricae Praecepta, Pars III De Panegyrico seu Laudatione. Pars I seems to be Apparatus ad Fabulam et Narrationem. Fable is handled on 15-31. After the famous Greek definition of Theion done into Latin ( sermo falsus veritatem effingens ), the author distinguishes rational (human) and moral (animal) fables, with mixed fables including both. He holds (19) that the sense of the fable generally needs to be expressed; otherwise people often miss the point of a fable. His Latin for promythium is praefabulatio, for epimythium affabulatio. Apologus and parabola are identical for him with fabula. After describing the qualities and uses of fables, the author presents some nine fables that exemplify various levels of style, twice telling the same stories on two levels (WL and FC). The last example is of the florid style: The Silkworm and the Spider takes four pages to tell! I found this book sitting in a box of disparate, unmarked, old books. It pays to look!This is a hardbound book (hard cover)Language note: Bilingual: Greek/LatinElzevers
Searches for New Physics effects in b →sl-sl+ transitions
No full textThe dissertation aims at presenting the current situation in the measurements of electroweak
penguin diagrams dominated decays: b → sl−l+1 . These decays have been a smoking gun
for hunting for New Physics effects over many years, but in the last three years the research
on these phenomena has intensified due to new measurements. Enormous progress has
been made both on the theoretical and the experimental sides to understand the measured
deviations from the current Standard Model predictions, referred to in what follows as
“anomalies”. The author of this dissertation has been one of the main authors of the angular analysis
of B0→ K∗ 0µ+µ− decay in the LHCb experiment, which has been widely regarded as one
of the most important results of the flavour physics sector in recent years. He has proposed
a method called “the method of moments” to measure the angular terms of this decay,
which he has later successfully applied in the measurement itself. Moreover, he has been
the driving force behind the two other important analyses in LHCb: the measurement of
the angular distribution and branching ratio of the B0→ K∗ 0 (1430)µ+µ− decay, where again the method of moments has been used to obtain the angular coefficients, and the search for the light scalar particle that can be produced in the b → s transitions and that decays to a dimuon pair. In this case no signal has been observed and the upper limits on the branching fraction have been set, later to be used for constraining the inflaton model.
The dissertation is organized as follows: the brief introduction is followed by, the second
chapter devoted to a theoretical description of rare B decays, where the effective field
theory formalism is introduced. Furthermore, the author discusses the current theoretical
problems in calculating the Standard Model predictions for the b → sl−l+ processes. Last but not least, the optimised angular observables that are less dependent on the form
factors uncertainness are derived. The third chapter describes the experimental apparatus
used in the b → sl−l+ measurements. Special focus is put on the sub-detectors that play
an important role in the studies of b → sl−l+ transitions. Chapters 4, 5, 6 are devoted to
describing the data analyses performed by the author in the LHCb experiment. In Chapter 7
the global analysis of electroweak penguin decays is presented. This kind of global analysis
has become extremely popular in the past few years as it helps to constrain and pin down those New Physics models that are likely to be responsible for the observed anomalies. The
author of this monograph is involved in one of the biggest collaborations performing New
Physics fits, where he is the convenor of the Flavour Working group. Furthermore, the
author presents his own study on separating the long distance effects in the B0→ K∗ 0µ+µ−decay. This is the state of the art way of determining those contributions. The chapter ends with a description of possible New Physics models that can explain the observed discrepancies
contravariant function-valued valuations on polytopes
No full textWe present a complete classification of contravariant,
-valued valuations on polytopes, without any
additional assumptions.It extends the previous results of the second author
[Int. Math. Res. Not. 2020] which have a good connection with the and
Orlicz Brunn-Minkowski theory. Additionally, our results deduce a complete
classification of contravariant symmetric-tensor-valued
valuations on polytopes
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