2,267 research outputs found
Pavonia salmonea Grings & Boldrini 2012, sp. nov.
No full textPavonia salmonea Grings & Boldrini, sp. nov. (Figure 1 and 3 A–D) Affinis Pavoniae guerkeanae sed ab ea mericarpiis minoribus plerumque non apiculatis, plerumque sine tuberculiis lateralibus acutis, nervo medio lato, compresso, rugosis, foliis trichomatibus stellatis longioribus, epicalice bracteolis lanceolatis vel ovato-lanceolatis, corolla salmonea, differt. Type:— BRAZIL. Santa Catarina: Bom Jardim da Serra, s.l., 28º23.488 S 49º33.772 W, 27 February 2009, 1333 m, M. Grings, R.B. Setubal & L.C.P. Lima 661 (holotype ICN!, isotypes CTES!, SP!, NY!). Subshrubs or shrubs up to 1.6 m tall; stems densely covered with long stellate trichomes. Leaf blades lanceolate, subtriangular to oval-lanceolate, seldom suborbicular, 0.5–6.0 × 0.4–2.5 cm, base sagittate to subcordate, apex acute to subobtuse, margin crenate, sometimes serrate, palmately 5-nerved, both surfaces covered with long stellate trichomes, abaxial surface with simple trichomes on the main nerves, seldom sparse simple trichomes in the adaxial surface; petioles 0.4–2.5 cm long, covered with short stellate trichomes and with sparse long simple trichomes; stipules subulate 3–4 mm long with short stellate trichomes and seldom with simple trichomes in the apex. Flowers solitary in the leaf axils, peduncle 1.2–3.5 cm long, densely covered with stellate trichomes, longer in the apex, along with long simple trichomes; epicalyx bracts 5, oval-lanceolate to slightly ovate, 4–7 × 2–4 mm, covered with short stellate trichomes, with long stellate trichomes and with some simple and long trichomes in the base; calyx 6–9 mm long, covered with stellate and some simple trichomes, both long and on the nerves; corolla salmon-pink, petals 1.5–2.5 × 1.4–2.4 cm, veins vinaceous, with basally vinaceous center; staminal column 7–8 mm long; free parts of the stamens 2–3 mm long; styles 3–4 mm longer than the staminal column. Mericarps 3.5–4.5 × 2.5–3.0 mm, muticous (seldom apiculate), sparsely pubescent, tuberculate, seldom with acute tubercles, median nerve wide, compressed and rugose. Seeds smooth and tufted at each end of the hilum. Distribution: — Brazil, Brazilian Atlantic Rainforest biome (IBGE 2004), in Santa Catarina and Rio Grande do Sul states (Figure 4). Phenology: —Flowering and fruiting specimens have been collected from November to April. Habitat: —In highland grasslands, scrub, rocky grasslands and in edges of Araucaria forest. Etymology: —From the Latin “ salmoneus ”, referring to the salmon-pink color of the flowers. Additional specimens examined (paratypes): — BRAZIL. Rio Grande do Sul: Bom Jesus, road Bom Jesus-São Joaquim, between Santo Inácio and Cerquinha river S 0580537 W 6843726 UTM, 24 January 2010, M. Grings & A. M. Z. Lunkes 969 (ICN); Canela, s.l., February 1986, M. Sobral & R. Silva 4942 (ICN, CTES); Jaquirana, Parque Estadual do Tainhas, S 29º04'47.5" W 050º21'57.3", 08 January 2010, M. Grings & G.B. Stahlberg 938 (ICN); São Francisco de Paula, Josafá, April 1984, M. Sobral 2976 (ICN), Josafá, S 29º21'45.3" W 50º04'51.6", 09 January 2010, M. Grings, G.B. Stahlberg, I. Buffon, S. Kronbauer & R.C. Printes 934 (ICN), Taimbé, 23 February 1960, A. Sehnem 7649 (PACA), Taimbesinho, 14 February 1946, B. Rambo 32199 (PACA); São José dos Ausentes, 4 Km from “Desnível dos rios”, S 28º35'08.6" W 49º57'31.5", 27 December 2009, M. Grings & N. J. Grings 894 (ICN); Santa Catarina: Bom Retiro, Campos Novos do Sul, 09 March 2005, G. Hatschbach, A.C. Cervi & E. F. Costa 78960 (MBM), begin of road to Urubici, 15 February 1995, G. Hatschbach et al. 61625 (MBM, HUCS); Lages, 14 Km E de Lages, road to São Joaquim, 24 November 1980, A. Krapovickas & R. Vanni 36886 (MBM); São Joaquim, Passo das Contas, 29 January 1950, R. Reitz 4992 (PACA); Urubici, 08 February 2007, G. Hatschbach & O. S. Ribas 79708 (MBM), 16 February 1995, G. Hatschbach & O.S. Ribas 61681 (MBM), Parque Nacional de São Joaquim, 10 February 2007, G. Hatschbach & O.S. Ribas 79882 (MBM), Morro da Igreja, 1820 m, 24 May. 1991, D. B. Falkenberg 5516 (FLOR). Pavonia salmonea is similar to P. guerkeana R.E. Fries (1908: 57) and to P. dusenii Krapovickas (1977: 313); specimens from different herbaria were sometimes identified as the first and sometimes as the later. The mericarps of P. salmonea are usually muticous (apiculate in a few specimens), somewhat smaller than those of P. guerkeana, usually without acute tubercles on each side of the median nerve, which is wide, compressed and rugose. The mericarps of P. guerkeana are always apiculate, with lateral acute tubercles and a narrow and smooth median nerve. Conversely, the mericarps of P. dusenii are strongly tuberculate and the median nerve is little prominent. Concerning the indumentum of the leaf blades, the stellate trichomes of P. salmonea are larger and denser than those of P. guerkeana. On the other hand, in P. dusenii the trichomes of the leaf blades are shorter than those of P. salmonea and P. guerkeana, and the indumentum is tomentose. The color of the corolla also differs, all three species having petals with wine-colored veins and claw, but in P. salmonea the ground-color of the petals is salmon-pink, in P. guerkeana white to pale-pink, and in P. dusenii rose-pink.Published as part of Grings, Martin & Boldrini, Ilsi Iob, 2012, Two new species of Pavonia section Lebretonia subsection Hastifoliae (Malvaceae: Malvoideae) from southern Brazil, pp. 38-46 in Phytotaxa 39 on pages 39-41, DOI: 10.11646/phytotaxa.39.1.3, http://zenodo.org/record/489472
Apobaetis biancae Cruz & Boldrini & Hamada 2020, sp. nov.
No full textApobaetis biancae sp. nov. Boldrini (Figs 2 A–2J, 4A, 4B) Apobaetis sp. nov. A in Boldrini & Cruz 2014: 4 Diagnosis. Larva. 1) labrum rectangular, distal margin without shallow medial emargination, medial area of distal margin with four robust pointed setae (Fig. 2A); 2) maxillary palp long, more than 2.5× the length of galea-lacinia, segment I slightly longer than galea-lacinia (Fig. 2D); 3) lingua subquadrate with one medial lobe (Fig. 2E); 4) glossa distally rounded; 5) inner projection of labial palp segment II rounded, segment III triangular (Fig. 2F); 6) tarsal claws 1.4× the length of tarsus, without row of denticles (Fig. 2G); 7) posterior margin of tergum IV with triangular spines (longer than wide) (Fig. 2H). Description. Larva. Body: 4.0– 4.2 mm; cercus approximately 1.5 mm. Body whitish (Fig. 4 A–B). Head. Antenna with minute spines on the apex of each segment. Frontal keel absent. Labrum (Fig. 2A): rectangular; distal margin without shallow medial emargination and medial lobe; distolateral area and distal margin with robust setae; medial area of distal margin with four robust setae on dorsal surface; ventral surface with one row of thin setae on medial area near distal margin. Left mandible (Fig. 2B): outer and inner sets of incisors with 5 and 3 denticles, respectively; prostheca robust, bifid at apex, inner margin frayed at middle; margin between prostheca and mola concave, with frayed lobe close to subtriangular process; tuft of robust setae at base of mola present; subtriangular process wide; denticles of mola not constricted; lateral margin convex. Right mandible (Fig. 2C): outer and inner sets of incisors with 3 denticles each; prostheca slender, bifurcated at apex; margin between prostheca and mola concave; tuft of setae at base of mola absent; denticles of mola constricted; lateral margin convex. Maxilla (Fig. 2D): maxillary palp long, more than 2.5× the length of galea-lacinia; segment I slightly longer than galea-lacinia, segment II without distal constriction; maxillary palp with scarce, thin, simple setae scattered over the surface. Hypopharynx (Fig. 2E): lingua subquadrate and longer than superlingua, with one medial lobe and without distal tuft of setae; superlingua not expanded, with short, thin, simple setae scattered over distal margin. Labium (Fig 2F): glossa narrowing slightly distally with apex rounded, longer than paraglossa; dorsal surface with one arc of setae on distal half, from inner to outer margin; ventral surface covered with small robust setae (not completely illustrated). Paraglossa curved inward; dorsal surface with three robust setae on apex and with one longitudinal row of five robust setae near inner margin; outer margin with one row of 14 robust setae; ventral surface with one longitudinal row of five robust setae in the middle. Labial palp with segment I shorter than the length of segments II and III combined; inner projection of labial palp of segment II rounded and laterally directed, outer margin and projection covered with thin, long, simple setae; ventral surface of segment II with of thin, long setae near the outer margin; segment III triangular, covered with thin, long, simple setae on outer margin, dorsal surface with one row of nine robust setae, outer margin concave. Thorax. Foreleg (Fig. 2G). Femur: with one row of 14 short robust setae on dorsal margin. Tibia: ventrally with one row of four short robust setae. Patella-tibial suture from dorsal to ventral margin. Tarsus: ventrally with one row of 12 short robust setae. Tarsal claws 1.4× the length of tarsus, row of denticles absent. Abdomen. Terga II and VII with a reddish medial mark, tergum V with a reddish lateral mark, terga IX and X reddish. Tergal surface covered by scale-like triangular spines (Fig. 2H); posterior margin with triangular spines (longer than wide) (Fig. 2H). Gill VI (Fig. 2I) oblong. Paraproct (Fig. 2J) with four marginal spines, posterolateral extension without spines. Cerci and paracercus with lateral spines on all segments. Comments. This species is found with low abundance on the sand bottom of a small stream. Etymology. After Bianca M. P. O. Boldrini, friend, wife of second author (R.B.), a great teacher and a fellow scientist, who gives him all the support needed. Material examined. Holotype, one larva in alcohol, Brazil, Rondônia, Colorado do Oeste, Rio Cabixi, S 13°15’31.8” / W060°20’04.8”, 06.ix.2012, Boldrini, R., Fernandes, A.S., Hamada, N., Nascimento, J.M.C. cols, INPA. Paratypes, same data as holotype, one larva in alcohol and two mounted on slides, UFRR.Published as part of Cruz, Paulo Vilela, Boldrini, Rafael & Hamada, Neusa, 2020, Redescription of Apobaetis lakota McCafferty, 2000 (Ephemeroptera: Baetidae) and description of two new species from Brazil, pp. 249-258 in Zootaxa 4885 (2) on pages 252-254, DOI: 10.11646/zootaxa.4885.2.6, http://zenodo.org/record/429658
Autobiographies of Others: Historical Subjects and Literary Fiction.
No full textIn this volume, Boldrini examines "heterobiography"—the first-person fictional account of a historic life. Boldrini shows that this mode is widely employed to reflect critically on the historical and philosophical understanding of the human; on individual identity; and on the power relationships that define the subject. In such texts, the grammatical first person becomes the site of an encounter, a stage where the relationships between historical, fictional and authorial subjectivities are played out and explored in the ‘double I’ of author and narrating historical character, of fictional narrator and historical person. Boldrini considers the ethical implications of assuming another’s first-person voice, and the fraught issue of authorial responsibility. Constructions of the body are examined in relation to the material evidence of the subject’s existence. Texts studied include Malouf’s An Imaginary Life, Carey’s True History of the Kelly Gang, Ondaatje’s The Collected Works of Billy the Kid, Adair’s The Death of the Author, Banti’s Artemisia, Vázquez Montalbán’s Autobiografía del general Franco. Also discussed, among others: Yourcenar’s Memoirs of Hadrian, Tabucchi’s The Last Three Days of Fernando Pessoa, Giménez-Bartlett’s Una habitación ajena (A Room of Someone Else’s).
Contents:
Introduction: The Portrait of a Voice
1. Heterobiography and The Utopia of Man
2. Heterobiography, Violence, and the Law
3. The Madness of the Documentary and the Aesthetics of the Body
4. The Author? In Theory, Dead: Heterobiography and Responsibility
5. The Polluted Swamp: Heterobiography, Dialogue, and History.
Conclusions
Rivudiva amazona Cruz & Boldrini & De Lima & Hamada 2022, sp. nov.
No full textRivudiva amazona sp. nov. urn:lsid:zoobank.org:act: 595B6165-BC4E-4AFB-BF4F-CD6FB5C22432 Figs 4–7 Rivudiva trichobasis – Falcão et al. 2011: 539. Diagnosis NYMPH. The combination of the characters: 1) labrum with distal margin straight (Fig. 4A); 2) labrum ventral surface with robust, distally bifid, eventually pectinated, setae on distal margin (Fig. 4A); 3) left mandible with incisors fused at basal third (Fig. 4B); 4) maxillary palp segment II with reduced apical lobe (Fig. 4D); 5) hypopharynx without distomedial projection (Fig. 4F); 6) glossa oval with inner and outer arcs of setae not sinuous and close to margins (Fig. 4G–H); 7) labial palp segment III robust, conical and apically pointed (Fig. 4G); 8) dorsal margin of forefemur with one row of long setae from middle length to apex (Fig. 5A); 9) forefemur on anterior surface with long blunt setae at middle (Fig. 5A); 10) patella-tibial suture present; 11) distal margin of terga with elongated triangular spines (Fig. 6A). Etymology The name ʻ Amazonas ʼ was given to native South American women after they attacked a conquest expedition. This species is named in honor of these brave native women. Name in apposition. Material examined Holotype BRAZIL • nymph on slide; Roraima, Caroebe, River Caroebe, vicinal 05; 00°54′47.3″ N, 59°34′19.9″ W; 19 Mar. 2013; P.V. Cruz, N. Hamada, R. Boldrini and G. Petronilo leg.; sand; INPA. Paratypes BRAZIL • 14 nymphs; same collection data as for holotype; INPA • 2 nymphs on slide; same locality as for holotype; 12 Mar. 2018; P.V. Cruz and I.O. Fernandes leg.; sand; INPA. Additional material BRAZIL • 4 nymphs; Roraima, BR-170, 41 Km turn to BR-432, old bridge, right from Vila de Santa Rita; 02°08′59.9″ N, 60°40′39.9″ W; 28 Mar. 2012; P.V. Cruz, N. Hamada, R. Boldrini and G. Petronilo leg.; sand; INPA • 3 nymphs; Roraima, Pacaraima, River Ereu; 04°02′02.9″ N, 61°23′09.5″ W; 26 Mar. 2012; P.V. Cruz, N. Hamada, R. Boldrini and G. Petronilo leg.; INPA • 3 nymphs; Roraima, São João da Baliza, Ramal 27, stream Lajinha; 01°00′59.7″ N, 59°55′53.1″ W; 24 Mar. 2012; P.V. Cruz, N. Hamada, R. Boldrini and G. Petronilo leg.; INPA • 1 nymph; Roraima, Caroebe, Ramal 37, River Caroebe, Cachoeirinha farm; 00°57′09.2″ N, 59°37′00.5″ W; 23 Mar. 2012; P.V. Cruz, N. Hamada, R. Boldrini and G. Petronilo leg.; INPA. Description Nymph LENGTH. Body, 3.3–3.5 mm. HEAD. Antenna. Scape and pedicel with spine-like setae; flagellum with minute spines on apex of each segment. Labrum (Fig. 4A). Rectangular, length about 0.6× maximum width; distal margin straight, one row of robust, distally bifid, eventually pectinated, setae from lateral to middle of distal margin; one row of thin bifid setae on distal margin not reaching distolateral margin; dorsal surface, near distal margin, with one row of thin setae, and many thin setae over surface (not illustrated). Left mandible (Fig. 4B). Incisors partially cleft in two sets (fused at basal third); outer and inner sets of incisors respectively with 4 + 3 denticles, outer incisor with spine-like process; prostheca robust and pectinated; margin between prostheca and mola straight; tuft of spine-like setae at base of mola present; subtriangular process wide; denticles of mola constricted; mola with one large denticle; outer margin convex. Right mandible (Fig. 4C). Incisors fused at base; outer and inner sets of incisors respectively with 3 + 3 denticles, outer incisor with spinelike process; prostheca stout, bifurcated at apex, inner lobe longer; margin between prostheca and mola almost straight; tuft of spine-like setae at base of mola present; denticles of mola not constricted; apex of mola with one simple setae; first process of mola rounded, second expanded and straight; outer margin convex. Maxilla (Fig. 4D–E). Maxillary palp 1.7× length of galea-lacinia; segment II 1.1× length of segment I; segment II inner margin straight, outer margin on apex straight, reduced apical lobe; ventral canine enlarged, not laterally expanded; set of distal setae of inner-ventral row rounded. Hypopharynx (Fig. 4F). Lingua longer than superlingua, sub-quadrangular without distomedial projection covered by tuft of simple setae; superlingua with rounded outer margin; short, thin, simple setae scattered over distal margin of lingua and superlingua. Labium (Fig. 4G–H). Glossa oval, slightly broad at base, distally rounded, shorter than paraglossa; inner margin without row of setae; ventral surface covered by thin setae; dorsal surface with inner arc close to inner margin, and outer arc not sinuous and close to outer margin; one small robust blunt seta on apex. Paraglossa curved inward; apex with one row of robust and long spine-like setae; outer margin without setae; dorsal surface with two longitudinal rows of setae, one near to inner margin, one near to outer margin, distally with long robust setae; ventral surface with one row of five setae near to ventral margin. Labial palp with segment I 0.8× length of segments II and III combined; inner distal protuberance of segment II rounded, with almost straight distal margin, covered with thin setae; segment III robust, conical, and apically pointed; outer margin with short thin setae, dorsal surface with one row of short spine-like setae near inner margin, ventral surface with one row of setae. THORAX. Foreleg (Fig. 5A–C). Femur length about 2.6× maximum width; dorsal row of setae from distal half to apex; anterior surface with one medial row of long blunt setae, one row of short blunt setae near dorsal margin; posterior surface with one row of long spine-like setae near ventral margin from base to apex, and one medial row of long spine-like setae. Tibia. Dorsally bare; ventral margin with one row of long spine-like setae, patella-tibial suture present. Tarsus. Ventral margin with one row of spine-like setae. Tarsal claws 0.4× length of tarsus, with two rows of conical denticles not reaching apex. Hind leg (Fig. 5D–E). Femur anterior surface with one row of spine-like setae near dorsal margin reaching apex, one row of long spine-like setae near ventral margin reaching apex, one row of spine-like setae near middle; posterior surface with one row of spine-like setae near ventral margin from base to apical third. Tibia. Dorsally bare; ventral margin with one row of small blunt setae, patella-tibial suture present. Tarsus. Ventral margin with one row of small blunt setae. Tarsal claws 0.4× length of tarsus, with two rows of small conical denticles not reaching apex. ABDOMEN. Terga (Fig. 7) with all segments white (color lost in alcohol), terga I–IX with two small medial dots, sometimes dots absent; tergum I with one large dot on disto-lateral margin (rare); eventually tergum II, III and IX darker or with large brown pigmentation; terga III and VI with one large medial mark near distal margin; terga VI and VII with disto-lateral transversal brown mark (rare). Posterior margin of terga with elongated triangular spines (Fig. 6A). Gills oblong, longer than next segment, with one medial trachea pigmented. Paraproct (Fig. 6B) with nine to eleven marginal spines, posterolateral extension with spines (broken in holotype and illustrated). Cerci (Fig. 6C) with lateral spines on every segment. Paracercus (Fig. 6D) without spines. Comments The differences in deepness of the curvature of the distal lobe on the maxillary palp segment II is related to the slide artifact (Fig. 4E).Published as part of Cruz, Paulo Vilela, Boldrini, Rafael, De Lima, Cláudia R. T. & Hamada, Neusa, 2022, It is a mess! How many species are in Rivudiva trichobasis Lugo- Ortiz & McCafferty, 1998 (Ephemeroptera: Baetidae)?, pp. 153-191 in European Journal of Taxonomy 789 (1) on pages 162-164, DOI: 10.5852/ejt.2022.789.1639, http://zenodo.org/record/596540
Autobiographies of Others Historical Subjects and Literary Fiction
No full textIn this volume, Boldrini examines "heterobiography"-the first-person fictional account of a historic life. Boldrini shows that this mode is widely employed to reflect critically on the historical and philosophical understanding of the human; on individual identity; and on the power relationships that define the subject. In such texts, the grammatical first person becomes the site of an encounter, a stage where the relationships between historical, fictional and authorial subjectivities are played out and explored in the 'double I' of author and narrating historical character, of fictional narrator and historical person. Boldrini considers the ethical implications of assuming another's first-person voice, and the fraught issue of authorial responsibility. Constructions of the body are examined in relation to the material evidence of the subject's existence. Texts studied include Malouf's An Imaginary Life, Carey's True History of the Kelly Gang, Ondaatje's The Collected Works of Billy the Kid, Adair's The Death of the Author, Banti's Artemisia, Vázquez Montalbán's Autobiografía del general Franco. Also discussed, among others: Yourcenar's Memoirs of Hadrian, Tabucchi's The Last Three Days of Fernando Pessoa, Giménez-Bartlett's Una habitación ajena (A Room of Someone Else's).Front Cover -- Autobiographies of Others -- Copyright Page -- Contents -- List of Images -- List of Abbreviations -- Acknowledgments -- Introduction: The Portrait of a Voice -- 1. Heterobiography and the Utopia of Man -- 2. Heterobiography, Violence, and the Law -- 3. The Madness of the Documentary and the Aesthetics of the Body -- 4. The Author? In Theory, Dead: Heterobiography and Responsibility -- 5. The Polluted Swamp: Heterobiography, Dialogue, and History -- Conclusions -- Notes -- Bibliography -- IndexIn this volume, Boldrini examines "heterobiography"-the first-person fictional account of a historic life. Boldrini shows that this mode is widely employed to reflect critically on the historical and philosophical understanding of the human; on individual identity; and on the power relationships that define the subject. In such texts, the grammatical first person becomes the site of an encounter, a stage where the relationships between historical, fictional and authorial subjectivities are played out and explored in the 'double I' of author and narrating historical character, of fictional narrator and historical person. Boldrini considers the ethical implications of assuming another's first-person voice, and the fraught issue of authorial responsibility. Constructions of the body are examined in relation to the material evidence of the subject's existence. Texts studied include Malouf's An Imaginary Life, Carey's True History of the Kelly Gang, Ondaatje's The Collected Works of Billy the Kid, Adair's The Death of the Author, Banti's Artemisia, Vázquez Montalbán's Autobiografía del general Franco. Also discussed, among others: Yourcenar's Memoirs of Hadrian, Tabucchi's The Last Three Days of Fernando Pessoa, Giménez-Bartlett's Una habitación ajena (A Room of Someone Else's).Description based on publisher supplied metadata and other sources.Electronic reproduction. Ann Arbor, Michigan : ProQuest Ebook Central, YYYY. Available via World Wide Web. Access may be limited to ProQuest Ebook Central affiliated libraries
First record of the genus Lumahyphes Molineri, 2004 (Ephemeroptera: Leptohyphidae) from Brazil with description of a new species
No full textBoldrini, R., Santos, G. C., Oliveira, D. R. (2015): First record of the genus Lumahyphes Molineri, 2004 (Ephemeroptera: Leptohyphidae) from Brazil with description of a new species. Zootaxa 4013 (1): 143-146, DOI: 10.11646/zootaxa.4013.1.1
G. Campo, R. Boldrini, M. Di Cesare, F. Basili, R. Moroni, M. Romanelli, E. Rizzuto, V. Trevisani, (2022). Certificato di assistenza al parto (CeDAP) 2021
No full textIl Rapporto CeDAP, a cura dell’Ufficio di Statistica del Ministero, illustra le analisi dei dati rilevati annualmente dal flusso informativo del Certificato di Assistenza al Parto (CeDAP), relativi all’evento nascita su tutto il territorio nazionale.
La rilevazione – istituita dal Decreto del Ministro della sanità 16 luglio 2001, n. 349. Regolamento recante “Modificazioni al certificato di assistenza al parto, per la rilevazione dei dati di sanità pubblica e statistici di base relativi agli eventi di nascita, alla natimortalità ed ai nati affetti da malformazioni” – costituisce a livello nazionale la più ricca fonte di informazioni sanitarie, epidemiologiche e socio-demografiche relative all’evento nascita, rappresentando uno strumento essenziale per la programmazione sanitaria nazionale e regionale
Il verso serpentino di Niccolò Perotti
No full textL’uso dell’aggettivo serpentinus per indicare un certo tipo di verso, o, meglio, di versificazione, non trova concordi i pochi studiosi che se ne sono occupati. L’indagine mostra come il versus serpentinus non vada confuso con il verso epanalettico: utilizzato da Marziale (IX 97), fu ripreso nel XV secolo in alcuni carmi dell’umanista Niccolò Perotti che curiosamente, però, non parla mai di questo verso nelle sue opere metriche
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