2,258 research outputs found
Due o tre cose sui Bembo, cremonesi
No full textIntroduzione al catalogo della mostra in cui si rende conto dei problemi critici legati alla bottega di Bonifacio Bemb
Monte S. Martino a Campi di Riva del Garda (TN): la fauna tra l’Età del Ferro e il Basso Medioevo
No full textMonte S. Martino è ubicato presso la frazione di Campi ad una quota compresa tra 600 e 850 m. La sua posizione è strategica per le comunicazioni e i commerci tra Lago di Garda e valle di Ledro, dalla valle del Chiese verso Brescia e dalle Giudicarie esteriori verso la valle di Non. I reperti faunistici esaminati sono stati rinvenuti durante gli scavi intercorsi tra 1996 e 2021 e rappresentano un campione che si presta ad essere analizzato dal punto di vista diacronico. Sono testimoniate, infatti varie fasi di vita del sito, sia cultuali durante la seconda età del Ferro e l’età romana, che abitative dall’epoca tardoantica al basso medioevo. I caprovini sono i domestici più presenti, seguiti da bovini, suini e dal pollame con percentuali differenti nel corso del tempo. Il cane è presente solo nel tardoantico e durante l’alto e il basso medioevo; gli equidi solo in età tardoantica; il coniglio in età tardoantica e durante il basso medioevo. Tra i selvatici il cervo è l’animale più attestato in tutti i periodi, mentre camoscio, capriolo, orso e scoiattolo solo in età tardoantica; il ghiro in età tardoantica e nel basso medioevo e il ratto solo nel basso medioevo.The archaeological site Monte S. Martino is near Riva del Garda at an altitude between 600 and 850 m. Its position is strategic for communications and trade between Lake Garda and the Ledro Valley, from the Chiese Valley towards Brescia and the External Giudicarie towards the Non Valley. The faunal remains examined were found during excavations between 1996 and 2021 and represent a sample that lends itself to being analyzed from a diachronic point of view. The site was a sanctuary during the Second Iron Age and the Roman Age, but it became a residential site during Late Antiquity and the Middle Ages. Sheep and goats are the most common domestic animals, followed by cattle, pigs and poultry, which have different percentages over time. The dog was present only in late antiquity and during the high and low Middle Ages; equids only in late antiquity; the rabbit in late antiquity and late Middle Ages. Among wild animals, the deer is the most attested animal in all periods, while the chamois, roe deer, bear and squirrel only in late ancient times; the dormouse in late antiquity and the late Middle Ages and the rat only in the late Middle Ages
I tarocchi dei Bembo. Dal cuore del Ducato di Milano alle corti della valle del Po
No full textBonifacio Bembo, cremonese, è il principale pittore tardogotico del ducato di Milano. Titolare, con i fratelli, di una bottega attrezzatissima, è al servizio di tre duchi: Filippo Maria Visconti, Francesco Sforza e Galeazzo Maria Sforza. Tra chiese e castelli, residenze ducali e scriptoria conventuali, feudatari e priori, la bottega è impegnata in un’attività variegata e quasi frenetica. I tarocchi, un’eccellenza tutta bembesca, sono “un sogno di profanità fulgida e assurda”, l’emblema effimero della “civiltà degli ori lombardi” evocata da Roberto Longhi. Partendo dalle carte viscontee del mazzo di Brera, affiancate da pochi, sceltissimi pezzi, tra pittura e “arti congeneri”, la mostra si propone di dipanare, per quanto possibile, alcuni dei molti problemi critici da sempre legati a Bonifacio e ai suoi fratelli
I corredi funerari con elementi d’ornamento in conchiglia della necropoli biritualistica del Bronzo medio e recente di Scalvinetto (Legnago, VR) e alcune note su conchiglie, conchiglie forate e oggetti d’ornamento in conchiglia nell’età del Bronzo dell’Italia settentrionale
No full textAsterocheres eugenioi Bandera & Conradi, 2014, sp. nov.
No full textAsterocheres eugenioi sp. nov. (Figs 2–5) Asterocheres suberitis Giesbrecht, 1897 in Norman and Scott 1906 Material examined.— holotype female (preserved in ethanol, NHM 1911.11.8.47277- 281) and 8 female paratypes plus one allotype male and 2 male paratypes (preserved in ethanol, NHM 1191.11.8.47277- 281) associated with Suberitis domuncula (Olivi), collected in Salcombe, Devon (Great Britain), on September of 1903 by Norman. Description of adult female. Body cyclopiform, slender with cephalothorax oval and cylindrical urosome (Fig. 2 A). Total length measured from rostral margin to posterior margin of caudal rami (excluding caudal setae) 585 µm; maximum width 384 µm. Ratio of length to width of prosome 1.1: 1. Ratio of length of prosome to that of urosome 2.6: 1. Prosome comprising cephalothorax fully incorporating first pedigerous somite and 3 free pedigerous somites. Epimeral areas of somites bearing legs 2 and 3 with pointed posterolateral angles (Fig. 2 A). Somite bearing leg 4 much smaller and narrower than preceding ones. Urosome 4 -segmented comprising leg 5 -bearing somite, genital double-somite and 2 free abdominal somites. Posterior margin of urosomites ornamented with hyaline frills with serrated free margins. Somite bearing leg 5 wider than long. Genital double-somite about 1.25 times wider than long, bearing genital apertures, paired gonopores located dorsolaterally; lateral margins with setular rows along distal third, posterior to genital apertures (Fig. 2 B). Each genital area armed with one plumose seta and one spiniform element. Integumental pores and sensilla present on urosomal somites (Fig. 2 B). Caudal rami 1.5 times longer than wide (Fig. 2 C); armed with 6 setae; seta I absent, setae II-VII all arranged around posterior margin with setae II and VII slightly offset onto dorsal surface. Antennule 21 -segmented (Fig. 2 D), about 270 µm long; segmental fusion pattern as follows: 1 (I)- 2, 2 (II)- 2, 3 (III)- 2, 4 (IV)- 2, 5 (V)- 2, 6 (VI)- 2, 7 (VII)- 2, 8 (VIII)- 2, 9 (IX-XII)- 7, 10 (XIII)- 2, 11 (XIV)- 1 + 1 spine, 12 (XV)- 2, 13 (XVI)- 2, 14 (XVII)- 2, 15 (XVIII)- 2, 16 (XIX)- 2, 17 (XX)- 2, 18 (XXI)- 2 + aesthetasc, 19 (XXII-XXIII)- 3, 20 (XXIV-XXV)- 3 and 21 (XXVI-XXVIII)- 6. Segment 10 (XIII) reduced, partly overlapped by distal expansion of compound segment 9 (IX-XII). Antenna biramous (Fig. 2 E), about 195 µm long; coxa unarmed, with few spinules; basis unarmed, with fine spinule rows. Exopod 1 -segmented, with one small lateral seta and two terminal setae. Endopod 3 -segmented; first segment elongate, ornamented with lateral rows of fine spinules; second segment produced distally on medial side but articulating with distal segment proximally on lateral side and armed with one smooth terminal seta. Third segment with distal claw and two subterminal plumose setae; claw provided with fine spinules on lateral margin. Siphon slender, about 195 µm long, reaching to posterior margin of intercoxal plate of leg 1. Mandible (Fig. 3 A) comprising stylet-like gnathobase and slender 2 -segmented palp. First segment of palp ornamented with rows of spinules; second segment with 2 plumose, unequal apical setae. Stylet with an expansion at the middle of its length. Maxillule bilobed (Fig. 3 B); praecoxal endite (inner lobe) more than three times longer than palp (outer lobe). Praecoxal endite armed with 5 distal setae, one of them smooth and short, ornamented with a row of long setules medially and a row of spinules on proximal outer margin. Palp armed with 3 terminal and one subterminal setae, all of them barbed. Maxilla (Fig. 3 C) 2 -segmented but with partial suture on syncoxa (proximal segment) possibly marking plane of praecoxa-coxa fusion; praecoxal portion bearing flaccid aesthetasc-like element medially, representing tubular extension of external opening of maxillary gland; coxal part unarmed but ornamented with few spinules proximally. Claw-like basis with recurved end and ornamented with spinules distally. Maxilliped 5 -segmented (Fig. 3 D) comprising short syncoxa, long basis and distal subchela consisting of 3 free endopodal segments armed with distal claw-like element. Syncoxa with one short seta distally; basis elongate and slender, with a row of spinules on lateral margin. First endopodal segment bearing two short setae and one longer distal seta; second endopodal segment armed with one medial seta. Third endopodal segment bearing recurved terminal claw plus additional subapical plumose seta. Distal margin of claw smooth. Legs 1-4 biramous (Figs. 4 A-D) with 3 -segmented rami. Intercoxal sclerite present in legs 1-4, ornamented with patches of spinules in leg 1. Spine and seta formula as Table 2. Coxae of legs ornamented with spinule rows laterally; coxal seta not present in leg 1. Outer spines of exopodal segments in legs 1-4 bilaterally serrate. Lateral margins of exopodal segments with minute serrations; lateral margins of endopodal segments with rows of setules. Fifth leg (Fig. 2 B) with protopodal segment incorporated into somite, with outer seta located dorsolaterally; elongate free segment, armed with two larger terminal setae and one shorter terminal seta, all of them smooth. Sixth leg (Fig. 2 B) represented by paired opercular plates closing off gonopores on genital double somite; leg armed with one plumose seta and one spiniform element. Adult male: Body cyclopiform (Fig. 5 A), slightly slender and shorter than female, with cephalothorax oval and cylindrical urosome. Body length 485 µm and greatest width 290 µm. Prosome comprising cephalothorax fully incorporating first pedigerous somite and 3 free pedigerous somites. Epimeral areas of somites bearing legs 2 and 3 with pointed posterolateral angles (Fig. 5 A). Somite bearing leg 4 much smaller and narrower than preceding ones. Urosome 5 -segmented comprising 5 th pedigerous somite, genital somite and 3 free abdominal somites. Genital somite about 1.2 times wider than long, bearing genital apertures posterolaterally on ventral surface (Fig. 5 B). Appendages as for female except for antennules, maxillipeds, and sixth leg. Antennule 18 -segmented (Fig. 5 C), about 260 µm long, geniculate; segmental fusion pattern as follow: 1 (I)- 2, 2 (II)- 2, 3 (III)- 2, 4 (IV)- 2, 5 (V)- 2, 6 (VI)- 2, 7 (VII)- 2, 8 (VIII)- 2, 9 (IX-XII)- 7, 10 (XIII)- 2, 11 (XIV)- 1 + 1 spine, 12 (XV)- 2, 13 (XVI)- 2, 14 (XVII)- 2, 15 (XVIII)- 2, 16 (XIX-XX)- 3, 17 (XXI-XXII)- 3 and 18 (XXIII-XXVIII)- 9. Geniculation located between segments 16 (XIX-XX) and 17 (XXI-XXII). Segment 10 (XIII) reduced, partly overlapped by distal expansion of compound segment 9 (IX-XII). Maxilliped 5 -segmented (Fig. 5 D), similar to that of female but basis with a small expansion provided with spinules in proximal half of medial region. Sixth leg (Fig. 5 B) forming large opercular plates closing off genital apertures, armed with 2 smooth setae, ornamented with rows of fine spinules. Etymology. This species is named after Eugenio Bandera, father of the first author. Distribution. United Kingdom (Norman and Scott 1906). Remarks. This species was reported by Norman and Scott in 1906 as Asterocheres suberitis Giesbrecht and was collected in a gathering from Salcombe in 1903. They pointed out that the usual habitat of these specimens was the water-passages of Suberites domuncula, and probably also of other sponges. However, a detailed comparison with the original description revealed that these specimens do not belong to Asterocheres suberitis but represent a new species, Asterocheres eugenioi sp. nov. The most striking features to distinguish these two species are: (1) The epimeral areas of somites bearing legs 2 and 3 have pointed posterolateral angles in A. eugenioi, thus contrasting with the rounded posterolateral corners of these somites in A. suberitis; (2) the inner maxillular lobe bears 4 distal setae in A. suberitis vs. 5 distal setae in A. eugenioi; (3) the maxillary proximal segment of the new species has a flexible setal element resembling an aesthetasc; this element is absent in A. suberitis; (4) the siphon reaches the posterior margin of the intercoxal plate of leg 1 in the new species but in A. suberitis it barely reaches the insertion of maxillipeds; (5) the leg 1 coxal seta is absent in A. eugenioi and it is present, short and plumose in A. suberitis (Taf. 2, I Asterocheres suberitis, Fig. 4; Giesbrecht 1899). This species belongs to a group of congeners possessing a 21 -segmented antennule in the female, 2 -segmented mandibular palp, and oral cone reaching the intercoxal plate of leg 1. This group is composed by six more species: A. urabensis Kim, 2004, A. hirsutus Bandera, Conradi & López-González, 2005, A. peniculatus Kim, 2010, A. ellisi Hamond, 1968, A. latus (Brady, 1872), and A. hoi Bandera & Conradi, 2013. There is no information about the length of the siphon in A. tenuicornis. However, this species can be easily separated from the new species due to the length of the caudal rami, six times longer than wide, the longest within the genus (Eiselt 1965). In contrast, caudal rami are only 1.5 times longer than wide in the new species. Among these six species, A. ellisi, A. urabensis and A. hoi have the caudal rami slightly longer than wide, shorter than A. eugenioi; and A. hirsutus and A. latus possess a caudal rami equal or longer than 2.5 times longer than wide, longer than in the new species and in A. peniculatus they are about as long as wide (Bandera & Conradi 2009 b; Kim 2004 a; Bandera & Conradi 2013; Bandera et al. 2005; Bandera & Conradi 2009 a; Kim 2010). Kim (2010) expressed the requirement of being strict with the definition of the genus Asterocheres, especially in reference to the setation on the rami of legs 1-4, which is quite conservative in this genus. There are only three species, together with the new species here described, with the coxal seta of leg 1 absent: A. pilosus Kim, 2004, A. trisetatus Kim, 2010, and A. fastigatus Kim, 2010. These species do not share any additional significant similarity which justify placing them in a separate genus, it is likely that this common characteristic is a homoplasy (Dr. I.-H. Kim pers. comm.). In addition, this group of seven species, including A. tenuicornis, can be distinguished from A. eugenioi sp. nov. by the shape of the body because the new species is the only one in the group with the epimeral areas of somites bearing legs 2 and 3 with pointed posterolateral angles, slightly produced into backwardly directed processes.Published as part of Bandera, Eugenia & Conradi, Mercedes, 2014, A new species of Asterocheres (Copepoda, Siphonostomatoida) with a redescription of A. complexus Stock, 1960 and A. sarsi Bandera & Conradi, 2009, pp. 542-558 in Zootaxa 3827 (4) on pages 546-551, DOI: 10.11646/zootaxa.3827.4.6, http://zenodo.org/record/22902
Translating Erlang to /spl mu/CRL
No full textThe language Erlang has been developed by Ericsson to implement large switching systems. Erlang is nowadays used by several companies for complex embedded systems. The language /spl mu/CRL is a process algebra with data. Several verification tools are available for /spl mu/CRL and other process algebras, including a tool to create labelled transition systems from /spl mu/CRL specifications. By having a translation from Erlang to /spl mu/CRL we can apply the verification tools for process algebras and labelled transition systems to industrial code. The translation is aware of the major design component in the switching software. This knowledge is used to ensure that the size of the labelled transition system generated by the tools is smaller than with a naive translation
Variedades bandera y aplicaciones armónicas
No full textIP 1102-05-10082Incluye anexos.v.1. Variedades bandera y aplicaciones / Marlio Paredes Gutierrez. -- v.2.Some results on the geometry of full flag manifolds and harmonic maps / Marlio Paredes. --v.3.Torneos yestructuras parabolicas sobre variedades bandera maximales / Marlio Paredes G. -- v.4. Soberun tipo especial de torneos y una clase de metricas sobre variedades bandera / Marlio Paredes, Patricia Gonzalez, Brendan MckayParedes. -- En: Revista Colombiana de Matematicas. -- Vol.24no. 2 (2000) ; p. 57-89. -- PONENCIA(S) EN;CONGRESO: Locally transitive tournaments and the geometryof maximal flagmanifolds / Marlio Paredes. -- En:;24 Coloquio Brasileiro de Matematica, Rio de Janeiro, 27 julhoa1 de agosto de 2003. -- Sobre un tipo;especial de torneos y una clase de metricas sobre variedades bandera / Marlio Paredes, Patricia gonzalez. --;En: Primera Conferencia Iberoamericana de matematica computacional, Bogotá, julio 25,26 y 27 de 2001 p. 125-1;superficie y con valores en una variedad bandera maximal /Marlio Paredes.-- En: Lecturas Matematicas. --;Vol. 24 (2003) ; p. 5-25. -- Variedades bandera maximales, torneos y aplicaciones armonicas / Marlio Paredes,;Sofia Pinzon. -- En: Revista Integracion. -- Vol. 18, no.2 (200) ; p. 40-52. -- Torneos y estructuras;parabolicas sobre variedades bandera maximales / Marlio ParedesG. -- En:Revista Integracion. -- Vol. 17, no.;1 (en-jun 1999) ; p. 1-48. -- Some results on the geometryoffull flag manifolds and harmonic maps / Marlio;ARTICULO(S) EN REVISTA: Families of (1,2)-simplectic metrics onfull flagmanifolds / Marlio Paredes. -- En:;IJMMS. -- Vol. 29, no. 11 (2002) ; p. 651-664. -- Estabilidaddeaplicaciones armonicas definidas sobre un
Variedades bandera y aplicaciones armónicas
No full textIP 1102-05-10082Incluye anexos.v.1. Variedades bandera y aplicaciones / Marlio Paredes Gutierrez. -- v.2.Some results on the geometry of full flag manifolds and harmonic maps / Marlio Paredes. --v.3.Torneos yestructuras parabolicas sobre variedades bandera maximales / Marlio Paredes G. -- v.4. Soberun tipo especial de torneos y una clase de metricas sobre variedades bandera / Marlio Paredes, Patricia Gonzalez, Brendan MckayParedes. -- En: Revista Colombiana de Matematicas. -- Vol.24no. 2 (2000) ; p. 57-89. -- PONENCIA(S) EN;CONGRESO: Locally transitive tournaments and the geometryof maximal flagmanifolds / Marlio Paredes. -- En:;24 Coloquio Brasileiro de Matematica, Rio de Janeiro, 27 julhoa1 de agosto de 2003. -- Sobre un tipo;especial de torneos y una clase de metricas sobre variedades bandera / Marlio Paredes, Patricia gonzalez. --;En: Primera Conferencia Iberoamericana de matematica computacional, Bogotá, julio 25,26 y 27 de 2001 p. 125-1;superficie y con valores en una variedad bandera maximal /Marlio Paredes.-- En: Lecturas Matematicas. --;Vol. 24 (2003) ; p. 5-25. -- Variedades bandera maximales, torneos y aplicaciones armonicas / Marlio Paredes,;Sofia Pinzon. -- En: Revista Integracion. -- Vol. 18, no.2 (200) ; p. 40-52. -- Torneos y estructuras;parabolicas sobre variedades bandera maximales / Marlio ParedesG. -- En:Revista Integracion. -- Vol. 17, no.;1 (en-jun 1999) ; p. 1-48. -- Some results on the geometryoffull flag manifolds and harmonic maps / Marlio;ARTICULO(S) EN REVISTA: Families of (1,2)-simplectic metrics onfull flagmanifolds / Marlio Paredes. -- En:;IJMMS. -- Vol. 29, no. 11 (2002) ; p. 651-664. -- Estabilidaddeaplicaciones armonicas definidas sobre un
Perder por bandera
No full textPerder por bandera está conformado por 15 pinturas en formatos cuadrados y rectangulares, Las pinturas están en lienzos convencionales de diversos tamaños, desde 2M cuadrados hasta piezas de 20x20cm, donde aparecen formas geométricas simples en colores primarios. Acompañado de un breve texto.Maestro en ArtePregrad
- …
