2,861 research outputs found
Matematica e dialettica. Rosmini e una possibile fonte della logica hegeliana
No full text(autore dei §§ 4-7 del saggio: A. Moretto; autore dei §§ 1-3 del saggio: F. Biasutti
Moretto and Romanino: religious painting in Brescia 1510-1550: identity in the shadow of La serenissima
No full textThis thesis examines several works of religious content produced by the Brescian painters Gerolamo Romano, 11 Romanino (148487-15'59) and Alessandro Bonvicino, 11 Moretto (1498-1554), produced for patrons and locations in Brescia between 15 10 and 1550. This enquiry has drawn on little used historical material in order to integrate the discussion of the images into a wider social and historical context.
The key aim of this study is to establish how Romanino and Moretto defined a Brescian identity in art. This will be argued by using two different approaches in order to examine the existence, and the manifestations, of such a local identity One approach taken in this study is to look at groups of corporate patrons and to consider the works executed for them in terms of similarities of content. Chapters 2 and 3 in turn consider the works executed by Romanino and Moretto for the Congregations of Santa Giustina of Padua, and of San Giorgio in Alga. The second approach adopted for the purposes of examination of strategies for the establishment of a Brescian visual identity employed in this study is to focus on representations of the Eucharist. It will be shown that Moretto developed a new visual motif of the 'Eucharistic Christ' in response to the growing popularity of the Forty Hours devotion in Brescia
Medicina e classificazione delle scienze
No full textNell'articolo si esamina il problema della collocazione della medicina nella classificazione delle scienze tra Seicento e Ottocento. Sono prese in considerazione le proposte di organizzazione del sapere, e del posto in esse assegnato alla medicina, da parte dei filosofi F. Bacon, R. Descartes, Chr. Wolff, dello scienziato A.-M. Ampère, del medico H. Boerhaave con riferimento alla classificazione della medicina, e dalle sistemazioni presentate nell'Encyclopaedia di J.H. Alsted e nell'Encyclopédie curata da D. Diderot e J. D'Alembert. Si precisa che sono stati scritti da A. Moretto l'Introduzione e i §§ 3, 4
Il rapporto semplice
No full texta cura di F. CHIEREGHIN, trad. e commento di F. BIASUTTI, L. BIGNAMI, F. CHIEREGHIN, A. GAIARSA, M. GIACIN, F. LONGATO, F. MENEGONI, A. MORETTO, G. PERIN-ROSS
Digitonthophagus sahelicus Moretto, new species
No full textDigitonthophagus sahelicus Moretto, new species http://zoobank.org/urn:lsid:zoobank.org:act:659D2617-892E-4CA3-803B-A727B64D643C (Figs. 9, 27–28, 57, 73, 91–92, 121, 141–143; Map 4) Type locality. Toulfé (13°53’43”N 01°52’25”W), 300 m, Lorum, Burkina Faso. Diagnosis. Africa species; Male pronotal anterior angles surface sloping laterally and usually with a dark spot (Figs. 57); female vertex with horns (Fig. 73). Description. Holotype ♂ (Fig. 9). Measurements. Length 9.5 mm, width 5.5 mm. Head (Figs. 27–28). Anterior clypeal edge emarginate on median fifth in dorsal view; clypeofrontal carina nearly straight and extending to clypeal edge; vertex convex medially, surface with scabrous punctures. Horns long, divergent in frontal view, gradually tapering from base to apex, posterointernal edge unmodified basally, internal surface with numerous coarse granules. Genal edge slightly upturned and arcuate on anterior third, forming a broad angle with clypeal edge. Pronotum (Fig. 57). Surface with granulate punctures extending slightly beyond posterior half, with a few scattered simple punctures on posterior portion of disc, larger punctures absent posterolaterally, with distinct, minute punctures throughout. Anteromedian tubercle atrophied, forming a simply convex projection in lateral view, surface of tubercles covered with rather regular and fine squamiform granules; median longitudinal sulcus absent; surface behind the eyes with a small and shallow oval depression, surface of anterior angles irregularly sloping laterally; anterior half of lateral edge slightly sinuous in dorsal and lateral view; posterior angles simply arcuate in dorsal view. Anterior hypomeral ridge nearly straight posteriorly and abruptly arcuate anteriorly with anterior most portion crenulate, anterior hypomeral depression surface light in color. Elytra (Fig. 9). Interval 2 and 4 lacking fine granules from base to apex. Legs. Protibial apicointernal tooth enlarged, with dorsal ridge interrupted before apex. Aedeagus (Fig. 121). Parameres with dorsal and ventral edges slightly diverging toward apex in lateral view. Internal sac sclerites (Figs. 141–143). Axial sclerite strongly sclerotized, abruptly bent ventrally on apical third. Subaxial sclerite, extending straight past apex of right lateral fold apical portion, with villi on apical half. Frontolateral peripheral sclerite basoventral apophysis moderately developed; a single medioventral carinae present; right lateral fold short, produced into a rather large everted and open apically conical process with extremely irregular apical edge; left lateral lobe absent; subapicodorsal lobe membranous, narrow, not reaching anterior edge, apex set on left side in dorsal view; apical lobe elongate and round apically, directed obliquely on left side, apical villi regular in shape; subapicoventral lobe short not reaching apical edge of apical lobe, oriented obliquely and in line with ventrally folded left edge of apical lobe. Variation. Measurements (103 ♂♂, 111 ♀♀). Length: male 6.5–11.0 mm (9.5 ± 0.8 mm), female 7.5–11.0 mm (9.4 ± 0.7 mm). Female lectotype. Cephalic outline in dorsal view as in Fig. 73; vertex with horns low, very wide basally and tapering to apex, posterointernal edge lacking tooth basally; anterior pronotal surface (Figs. 91–92) with a single callus approximately half interocular distance in width, dorsal edge of callus weakly defined. Protibia short, with external teeth more robust. Primary type data. Holotype ♂ (CMNC): [BURKINA FASO: LORUM / Toulfé, 300m / 13°53’43”N 01°52’25”O / 18.VII.2006, zone sahélienne / steppe arborée, collecte géné- / rale, F. & S. Génier, 2006-43]; [COLÉOPTÈRES / DU / BURKINA FASO / BF008585] barcode label; [HOLOTYPE ♂ / Digitonthophagus / sahelicus n.sp. / des. P. Moretto, 2016] red card. Map 4. Distribution of Digitonthophagus sahelicus. Material examined (266 ♂♂, 193 ♀♀, 496 sex not recorded), distribution (Map 4): BURKINA FASO: HAUTS-BASSINS, Bobo-Dioulasso (11°12'N, 4°18'W), viii.2002, [anonymous] —1 ♀ (paratype) (PMOC); SAHEL, après le pont, route Essakane-Dori, Gorum-Gorum, 271 m (14°9'32.8''N, 0°1'20.4''E), 7.viii.2012, P. Moretto— 1 ♀, 1 ♂ (paratypes) (PMOC); Conseil régional, Dori, 283 m (14°2'4.5''N, 0°3'10.5''W), 23– 25.viii.2013, P. Moretto (2013-50)— 9 ♀♀, 9 ♂♂ (18 paratypes) (PMOC); Conseil régional, Dori, 283 m (14°2'4.5''N, 0°3'10.5''W), 30.viii.2013, P. Moretto— 1 ♀ (paratype) (PMOC); Dori (14°2'N, 0°1'W), iv.2007, [anonymous]— 8 ♀♀, 3 ♂♂ (11 paratypes) (JFJC); Essakane, Gorum-Gorum, 264 m (14°22'40.2''N, 0°5'47.7''E), 13–15.viii.2012, P. Moretto— 1 ♀, 1 ♂ (paratypes) (PMOC); N’djomga, Dori (14°3'55.7''N, 0°3'3.4''W), 24– 27.viii.2013, P. Moretto— 3 ♂♂ (3 paratypes) (PMOC); LOROUM, Toulfé, 300 m (13°53'43''N, 1°52'25''W), 16.vii.2006, F. & S. Génier (2006-38)— 24 ♀♀, 28 ♂♂ (52 paratypes) (FGIC); Toulfé, 300 m (13°53'43''N, 1°52'25''W), 16.vii.2006, F. & S. Génier (2006-40)— 2 ♀♀, 13 ♂♂ (15 paratypes) (FGIC); Toulfé, 300 m (13°53'43''N, 1°52'25''W), 17.vii.2006, F. & S. Génier (2006-41)— 2 ♀♀, 7 ♂♂ (9 paratypes) (FGIC); Toulfé, 300 m (13°53'43''N, 1°52'25''W), 18.vii.2006, F. & S. Génier (2006-43)— 23 ♀♀, 24 ♂♂ (holotype, allotype, 45 paratypes) (CMNC, FGIC); Toulfé, 300 m (13°53'43''N, 1°52'25''W), 18.vii.2006, F. & S. Génier (2006-42)— 4 ♂♂ (4 paratypes) (FGIC); NAHOURI, Forêt de Nazinga, Boulieselo, 310 m (11°11'50''N, 1°35'9''W), 27.vii.2006, F. & S. Génier (2006-82)— 2 ♂♂ (2 paratypes) (FGIC); CAMEROON: EXTREME NORTH, Waza National Park (11°15'N, 14°39'E), 18.viii.2006, C. Vanderbergh— 1 ♂ (paratype) (PMOC); CHAD: ENNEDI, Fada (17°11'N, 21°35'E), 9/4/1935, [anonymous]— 1 ♂ (paratype) (MNHN); HADJER-LAMIS, Sitje, rive sud Lac Tchad (12°53'N, 14°52'E), 11.viii.2006, C. Vanderbergh— 1 ♀, 2 ♂♂ (3 paratypes) (PMOC); KANEM, Zigueï (14°43'N, 15°47'E), 19–21.vii.1935, [anonymous] —1 ♀ (paratype) (MNHN); N’DJAMENA, Farcha (12°7'N, 14°59'E), vi.1968, [anonymous]— 1 ♀, 1 ♂ (paratypes) (MNHN); DJIBOUTI: DJIBOUTI, Djibouti (11°35'N, 43°9'E), [no date], [anonymous]— 4 ♀♀, 3 ♂♂ (7 paratypes) (IRSNB); ERITREA: ANSEBA, Hagaz (15°42'N, 38°16'E), vii.2003, M. Forti— 1 ♂ (paratype) (PMOC); GASH-BARKA, 18 km E Akordat (15°33'N, 38°1'E), vii.2003, M. Forti— 2 ♀♀, 3 ♂♂ (5 paratypes) (FGIC, PMOC); NORTHERN RED SEA, Nefasit (15°20'N, 39°4'E), vii.2002, Czeppel & Forti— 3 ♀♀, 3 ♂♂ (6 paratypes) (FETC); MALI: SEGOU, Sansanding (13°43'18''N, 6°0'11''W), [no date], R. Demange— 1 ♀ (paratype) (MNHN); MAURITANIA: Trarza Desert, [no date], [anonymous]— 2 ♀♀, 2 ♂♂ (4 paratypes) (IRSNB); ADRAR, Atar (20°31'N, 13°3'W), 24.ix.1968, P. Tauzin— 1 ♂ (paratype) (PMOC); INCHIRI, Oued Akjoujt (19°45'N, 14°23'W), x.1937, P. Malzy— 1 ♂ (paratype) (MNHN); NOUAKCHOOT, Nouakchoot (18°5'N, 15°59'W), 15.viii–30.ix.2006, Famille Stalmanns— 5 ♀♀, 1 ♂ (paratypes) (PMOC); SÉLIBABY, Tachoot [=Tassota Barene] (15°26'N, 12°16'W), 20.x.1941, [anonymous]— 1 ♂ (paratype) (OMOC); NIGER: AGADEZ, Agadez (16°58'N, 7°59'E), 1909, Cortier— 2 ♂♂ (2 paratypes) (MNHN); Agadez (16°58'N, 7°59'E), 2.viii.1947, L. Chopard & A. Villiers— 1 ♀ (paratype) (MNHN); Agadez (16°58'N, 7°59'E), 20.viii.1947, L. Chopard & A. Villiers— 1 ♂ (paratype) (MNHN); Agadez (16°58'N, 7°59'E), 25.viii.1947, L. Chopard & A. Villiers— 1 ♀ (paratype) (MNHN); Agadez (16°58'N, 7°59'E), 20.viii.1989, [anonymous]— 3 ♀♀, 1 ♂ (paratypes) (OMOC); Arlit (18°44'N, 7°23'E), 15.ix.1977, P. Tauzin— 1 ♀ (paratype) (PMOC); Dabaga, Aïr sud, 600 m (17°18'N, 8°10'E), 13–16.viii.1947, L. Chopard & A. Villiers— 2 ♂♂ (2 paratypes) (MNHN); Taquei, Aïr Massif (18°25'48''N, 8°24'36''E), 26.viii.1983, P.C. Matteson— 1 ♂ (paratype) (BMNH); DIFFA, N’Guigmi (14°15'N, 13°7'E), viii.1919, Dr. Noel— 7 ♀♀, 5 ♂♂ (12 paratypes) (MNHN); N’Guigmi (14°15'N, 13°7'E), ix.1919, Dr. Noel— 12 ♀♀, 13 ♂♂ (25 paratypes) (MNHN); N’Guigmi (14°15'N, 13°7'E), vi–vii.1919, Dr. Noel— 1 ♂ (paratype) (MNHN); N’Guigmi (14°15'N, 13°7'E), x.1919, Dr. Noel— 1 ♂ (paratype) (MNHN); DOSSO, Toudou (14°7'N, 3°54'E), 10.viii.1989, [anonymous] —1 ♀ (paratype) (OMOC); Toudou (14°7'N, 3°54'E), 13.viii.1989, [anonymous]— 2 ♀♀, 1 ♂ (paratypes) (OMOC); SENEGAL: [unspecified locality], [no date], [anonymous] —1 ♂ (paratype) (BMNH); DAKAR, Keur Ndiaye Lô (14°45'25''N, 17°14'11''W), 20.viii.2013, I. de Dinechin— 1 ♂ (paratype) (CMD); DIOURBEL, Bambey (14°42'N, 16°28'W), viii.1939, J. Risbec— 2 ♂♂ (2 paratypes) (BMNH); Bambey (14°42'N, 16°28'W), 1945, J. Risbec— 1 ♂ (paratype) (BMNH); FATICK, Diouroup (14°21'N, 16°32'W), 14–18.viii.2007, P. Moretto— 4 ♀♀, 9 ♂♂ (13 paratypes) (FGIC, PMOC); KAOLAK, Missirah, 45 m (13°59'26''N, 15°7'4''W), 16.vii.2007, F. Génier (2007-01)— 12 ♀♀, 9 ♂♂ (21 paratypes) (FGIC); LOUGA, Linguère (15°24'N, 15°7'W), ix.1967, A. Descarpentries, T. Leye & A. Villiers— 496 specimens (paratype) (MNHN); Ndam-Dam (15°36'22''N, 16°23'35''W), xi.1967, A. Descarpentries, T. Leye & A. Villiers— 2 ♀♀, 7 ♂♂ (9 paratypes) (MNHN); Ndilla (15°20'N, 15°3'W), ix.1967, A. Descarpentries, T. Leye & A. Villiers— 1 ♂ (paratype) (MNHN); SAINT-LOUIS, Commune de Saint-Louis, 7 m (16°4'34''N, 16°22'40''W), 27.viii.2009, F. Génier (2009-33)— 1 ♀ (paratype) (FGIC); Commune de Saint-Louis, 7 m (16°4'34''N, 16°22'40''W), 27.viii.2009, P. Moretto— 2 ♀♀, 2 ♂♂ (4 paratypes) (PMOC); Podor (16°39'N, 14°57'30''W), viii–ix.1911, R. Chudeau— 1 ♀ (paratype) (MNHN); Richard-Toll (16°28'N, 15°41'W), 7–10.viii.2008, P. Moretto— 1 ♀ (paratype) (PMOC); Richard-Toll (16°28'N, 15°41'W), 28–31.viii.2009, F. Génier (2009-38)— 8 ♀♀, 20 ♂♂ (28 paratypes) (FGIC); Richard-Toll (16°28'N, 15°41'W), 28–30.viii.2009, F. Génier (2009-40)— 4 ♀♀, 1 ♂ (paratypes) (FGIC); Richard- Toll (16°28'N, 15°41'W), 28.viii.2009, F. Génier (2009-36)— 1 ♂ (paratype) (FGIC); Richard-Toll (16°28'N, 15°41'W), 28.viii–1.ix.2009, P. Moretto & F. Génier— 1 ♀, 2 ♂♂ (3 paratypes) (PMOC); Richard-Toll (16°28'N, 15°41'W), 30.viii.2009, F. Génier (2009-43)— 2 ♀♀, 3 ♂♂ (5 paratypes) (FGIC); Richard-Toll (16°28'N, 15°41'W), 30.viii.2009, F. Génier (2009-44)— 3 ♀♀, 17 ♂♂ (20 paratypes) (FGIC); Richard-Toll (16°28'N, 15°41'W), 31.viii.2009, F. Génier (2009-48)— 6 ♂♂ (6 paratypes) (FGIC); Richard-Toll (16°28'N, 15°41'W), 1.ix.2009, F. Génier (2009-49)— 1 ♀, 4 ♂♂ (5 paratypes) (FGIC); Richard-Toll (16°28'N, 15°41'W), 1.ix.2009, F. Génier (2009-50)— 3 ♂♂ (3 paratypes) (FGIC); Richard-Toll (16°28'N, 15°41'W), 3.ix.2009, F. Génier (2009- 52)— 1 ♀, 1 ♂ (paratypes) (FGIC); Saint-Louis (16°0'30''N, 16°29'30''W), 1899, V. Planchat— 13 ♀♀, 19 ♂♂ (32 paratypes) (MNHN); THIÈS, Kayar (14°55'N, 17°7'E), viii.1971, A. Villiers— 1 ♀, 1 ♂ (paratypes) (OMOC); Mbour (14°25'N, 16°58'W), viii.1995, P. Moretto— 13 ♀♀, 8 ♂♂ (21 paratypes) (PMOC); Meckhé (15°7'N, 16°38'W), [no date], [anonymous]— 1 ♂ (paratype) (MNHN); Nianing, 8 m (14°19'N, 16°55'43''W), 23.vii.2006, A. Coache— 1 ♀, 1 ♂ (paratypes) (JFJC); SUDAN: KHARTOUM, Environs de Khartoum (15°35'N, 32°32'E), [no date], [anonymous]— 2 ♀♀, 1 ♂ (paratypes) (MNHN). Etymology. Sahelicus is a Latin adjective pertaining to the distribution of this species. Natural history. A mostly Sahelian species associated with grassland and wooded and acacia steppes habitats and grassland enclave within degraded sudanese vegetation and along dried sandy riverbeds, on deep sandy soils. Individuals are common at light traps and also collected from, donkey, cow, and human dung. Some individuals collected in pitfall traps baited with rumen content, recently killed toads and monitor lizards.Published as part of Génier, François & Moretto, Philippe, 2017, Digitonthophagus Balthasar, 1959: taxonomy, systematics, and morphological phylogeny of the genus revealing an African species complex (Coleoptera: Scarabaeidae: Scarabaeinae), pp. 1-110 in Zootaxa 4248 (1) on pages 21-24, DOI: 10.5281/zenodo.43944
MITOMYCIN C MODULATION OF CORNEAL WOUND HEALING AFTER PHOTOREFRACTIVE KERATECTOMY IN HIGHLY MYOPIC EYES
No full textOphthalmology. 2005 Feb;112(2):208-18; discussion 219.
Mitomycin C modulation of corneal wound healing after photorefractive keratectomy in highly myopic eyes.
Gambato C, Ghirlando A, Moretto E, Busato F, Midena E.
SourceRefractive Surgery Service and Antimetabolite Therapy Research Unit, Department of Ophthalmology, University of Padova, Padova, Italy.
Abstract
PURPOSE: To evaluate the role of topical mitomycin C in corneal wound healing (CWH) after photorefractive keratectomy (PRK) in highly myopic eyes.
DESIGN: Prospective, double-masked, randomized clinical trial.
PARTICIPANTS: Seventy-two eyes of 36 patients affected by high (>7 diopters) myopia.
METHODS: In each patient, one eye was randomly assigned to PRK with intraoperative topical 0.02% mitomycin C application, and the fellow eye was treated with a placebo. Postoperatively, mitomycin C-treated eyes received artificial tears (3 times daily, tapered in 3 months), whereas the fellow eye was treated with fluorometholone sodium 2% and artificial tears (3 times daily, tapered in 3 months).
MAIN OUTCOME MEASURES: Uncorrected visual acuity (UCVA) and best-corrected visual acuity (BCVA), contrast sensitivity, manifest refraction, and biomicroscopy. Contrast sensitivity was determined using the Pelli-Robson chart. Corneal confocal microscopy documented CWH.
RESULTS: Mean follow-up was 18 months (range, 12-36). No side effects or toxic effects were documented. At 12-month follow-up examination, UCVAs (logarithm of the minimum angle of resolution) were 0.4+/-0.48 and 0.5+/-0.53 (P = .03) in mitomycin C-treated eyes and corticosteroid-treated eyes, respectively. At 1 year, corneal haze developed in 20% of corticosteroid-treated eyes, versus 0% of mitomycin C-treated eyes. At 12, 24, and 36 months, corneal confocal microscopy showed activated keratocytes and extracellular matrix significantly more evident in untreated eyes (Ps = 0.004, 0.024, and 0.046, respectively).
CONCLUSION: Topical intraoperative application of 0.02% mitomycin C can reduce haze formation in highly myopic eyes undergoing PRK.
Comment in
Ophthalmology. 2006 Feb;113(2):357; author reply 357-8.
PMID: 15691552 [PubMed - indexed for MEDLINE
Il nuovo strumento EFSA per la valutazione dell’esposizione dell’operatore agricolo (AOEM 2012): confronto con i precedenti modelli
No full text
Can Supply Chain Finance help mitigate the financial disruption brought by Covid-19?
No full textThe Covid-19 pandemic created a financial disruption within supply chains, which is destabilizing especially small and medium enterprises (SMEs) and could be devastating for the global economy. Supply chain finance (SCF) was an answer to the 2008 financial crisis and could help facing the new challenge, but new paradigms are necessary, to become an effective mitigation strategy. Through the support of empirical data collected through a focus group with industry experts, this note presents new research directions in the SCF domain, based on Contingency Theory and Resource Orchestration Theory, including new solutions, actors, collaborations, technologies, regulations, and performance
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