139,964 research outputs found
Correspondencia del Conde de Lemos con D. Francisco de Lemos, su hermano, y con el príncipe de Esquilache (1613-1620)
No full textPaz y Meliá A. Correspondencia del Conde de Lemos con D. Francisco de Lemos, su hermano, y con el príncipe de Esquilache (1613-1620). In: Bulletin Hispanique, tome 5, n°3, 1903. pp. 249-258
Cédula ( d 1783-04-03)
No full textCertifica la copia Don Antonio de Lemos y BeltranPrecede al título una gruz griegaTexto fechado en Sevilla á tres de Abril del año de mil setescientos ochenta y tresSign. : A4Portada con escudo real xilográficoH Ca. 073/01
D. Francisco de Lemos. Perfil de um Reitor Reformador.
No full textEsta tese de mestrado pretende apresentar algumas conclusões sobre a vida de D. Francisco de Lemos. E num segundo momento pretende analisar a sua acção como Reitor da Universidade de Coimbra durante os seus dois reitorados
Dissertatio Inavgvralis Medico-Practica De Sterilitate Vtrivsqve Sexvs, Eivsqve Cavssis, Signis Et Cvratione
No full textHalle, Univ., Med. Diss., 1758Qvam ... Ivssv Et Avctoritate Gratiosae Facvltatis Medicae In Academia Regia Fridericiana ... Pro Gradv Doctoris ... D. XXII. Maii MDCCLVIII. Ervditorvm Censvrae Exhibvit Avctor Iosephvs De Lemos, Ivnior, Hambvrgensis, Gente IvdaevsNicht identisch mit VD18 14995514, dort ohne [2] Bl. Gratulationen und S. 32 ohne Kustode "Nobi-"Enth. 4 Gratulationsschreiben der BeiträgerVorlageform des Erscheinungsvermerks: Halae Magdebvrgicae, Ex Typographia Vesteriana
D. António Maria Tovar De Lemos Pereira, diplomata e colecionador = D. António Maria Tovar de Lemos Pereira, diplomat and collector
No full textApresentamos neste estudo dois vasos italiotas adquiridos no final do século XIX/início do século XX pelo diplomata D. António Maria Tovar de Lemos Pereira, 1.º Conde de Tovar. O primeiro exemplar corresponde a um Kratêr de sino apúlio, produzido entre 365-350 a.C., em Tarento, e atribuível ao Círculo do Grupo do Pintor do Vaticano V14. O segundo vaso corresponde uma pequena olpe italiota de verniz negro, de corpo ovalado e colo curto. O estudo do percurso histórico destes dois exemplares contribui para o melhor conhecimento sobre o colecionismo de vasos gregos em Portugal, no século XIX, comprovando que as coleções de antiguidades foram também relevantes em Portugal tal como no século XIX em outros países europeus.In this study we present two italiote vases acquired in the late 19th/early 20th century by the diplomat D. António Maria Tovar de Lemos Pereira, 1st Count of Tovar. The first specimen corresponds to an Apulian Red-Figure Bell-Krater made in Tarentum, dated between 365-350 BC, attributed to the Circle of the Vatican Painter's Group V14. The second vase is also an Apulian production and corresponds to a small italiote plain black olpe with an oval body and short neck. The study of the historical path of these two specimens allows us to gradually broaden our knowledge about the collection of Greek vases in Portugal in the 19th century, showing that the collections of antiquities were also relevant in Portugal in that century, as in other European countries
Ana Maria Bandeira estudia la correspondencia de D. Francisco de Lemos (MNMC)
No full textLos análisis de correspondencia histórica están de moda en el panorama académico internacional más puntero. Uno de los ejemplos que lo avala está representado por los estudios de Ana Maria Bandeira, archivera de la Universidad de Coimbra. Este sábado a las tres y media la estudiosa presentará, en el Museo Nacinal de Machado de Castro, un avance sobre el estudio inédito de casi cincuenta cartas de Francisco de Lemos, en la conferencia titulada "Um outro olhar sobre D: Francisco de Lemos". Tale..
Exocora girotii Lemos & Brescovit, 2013, new species
No full text<i>Exocora girotii</i> new species <p>Figs 4 A–D; 5A–F; 15B; 16B; 17</p> <p> <b>Types:</b> Holotype 1ɗ, from Fazenda Angelim (23º23'49"S; 45º03'51"W), Ubatuba, São Paulo, Brazil, 13–16/II/ 2012, A. M. Giroti col. (IBSP 161827). Paratype: 1Ψ, from Estação Ecológica da Juréia-Itatins (24º33'S; 47º13'W), Peruíbe, São Paulo, Brazil, 26/IV–3/V/1999, A. D. Brescovit <i>et al</i>. col. (IBSP 24852); 2Ψ, from Reserva Natural da Serra do Itaqui (25°18'25''S; 48°19'44''W), Guaraqueçaba, Paraná, Brazil, IX/2007, E. F. Ramos col. (IBSP 143750); 1Ψ, from Reserva Natural do Rio Cachoeira (25°25'44''S; 48°42'43''W), Antonina, Paraná, Brazil, 24/IX/2005, E. Álvarez col. (MCN 44720); 1Ψ, from Parque Estadual da Serra do Tabuleiro (27°52'14"S; 48°47'10"W), Paulo Lopes, Santa Catarina, Brazil, 10–20/II/2002, Equipe Biota col. (IBSP 143792).</p> <p> <b>Etymology:</b> The species name is in honor of André Marsola Giroti, for his effort in finding <i>Exocora</i> whenever he is in the field, and is a noun in the genitive.</p> <p> <b>Diagnosis:</b> Males of <i>Exocora girotii</i> <b>n. sp.</b> are distinguished from those of other species in the genus, except <i>E. ribeiroi</i> <b>n. sp.</b>, by the shape of the lamella characteristica, with proximal part globose, and by the short embolic membrane (Figs 4 A, B). Females are diagnosed by the curved shape of the posterior margin of ventral plate, by the very narrowed dorsal plate and by the shape of the copulatory ducts, long and coiled (Figs 4 C, D; 15B; 16B). <i>Exocora girotii</i> can be distinguished from <i>E. ribeiroi</i> <b>n. sp.</b> by the twisted distal part of lamella characteristica (Figs 4 A, B), by its wider atrium (Figs 4 C; 15B), and by the closer distance between the copulatory ducts (Figs 4 D; 16B).</p> <p> <b>Description: Male (Holotype IBSP 161827):</b> Total length 1.52. Carapace 0.76 long, 0.62 wide, yellowish, with dark spots on the lateral. Sternum 0.42 long, 0.44 wide, yellowish with dark margins. Clypeus 0.16 high. Chelicerae promargin with three teeth, retromargin with four teeth. Abdomen pale brown, with many dark marking along the entire surface (Figs 5 A, B). Eyes diameter and interdistances: AME 0,0 6, ALE 0.09, PME 0.09, PLE 0.09, AME-AME 0.01, PME-PME 0.02, AME-ALE 0.02, PME-PLE 0.04. Eyes grouped, projected above the clypeus, ocular area with few bristles (Fig. 5 B). Coxa IV separation 1.1 times their width. Femur I/II/ III/IV 0.92/0.86/0.58/0.78; patella I 0.28; tibia I 0.88; metatarsus I 0.96; tarsus I 0.62. Legs yellow with dark spots on each article. Prolateral macroseta, thick and curved, on tibia I (Fig. 5 C). TmI 0.21. Palpal tibia without apophysis. Protegulum present. Embolic division with small radix. Embolus long, filiform and free, origin from the posterior side of the embolic division, runs to the ectal side curving several times (Figs 4 A, B).</p> <p> <b>Female (Paratype IBSP 143792):</b> Total length 1.96. Carapace 0.74 long, 0.56 wide. Sternum 0.42 long, 0.44 wide. Clypeus 0.1 high. Chelicerae promargin with 3 teeth, retromargin with 5 teeth. Body color pattern same as male, but darker and with white spots on the abdomen (Figs 5 D, E). Eyes diameter and interdistances: AME 0.06, ALE 0.1, PME 0.09, PLE 0.09, AME-AME 0.01, PME-PME 0.02, AME-ALE 0.02, PME-PLE 0.02. Eyes pattern as in male (Fig. 5 E). Coxa IV separation 1.16 times their width. Femur I/II/III/IV 0.82/0.78/0.6/ 0.78; patella I 0.24; tibia I 0.72; metatarsus I 0.72; tarsus I 0.5. Legs as in male, tibia I prolateral macroseta thinner and straight (Fig. 5 F). TmI 0.25. Epigynum prominent (Figs 4 C; 15B). Spermathecae oblong. The long and coiled copulatory ducts originate in the ventral part of the spermathecae. Fertilization ducts mesally oriented, originating from the dorsal part of the spermathecae (Figs 4 D; 16B).</p> <p> <b>Variation:</b> Males (n=2): Total length 1.18–1.52; carapace length 0.76–0.78; carapace width 0.62–0.66; femur I length 0.92–0.92. Females (n=7): Total length 1.78–2.16; carapace length 0.72–0.9; carapace width 0.64–0.72; femur I length 0.82–0.94.</p> <p> <b>Distribution:</b> States of Rio de Janeiro, São Paulo, Paraná, Santa Catarina, in Brazil (Fig. 17).</p> <p> <b>Material examined (N=9):</b> BRAZIL, <b>Paraná:</b> Antonina, Reserva Natural do Rio Cachoeira, (25°25'44''S; 8°42'43''W), 2Ψ, 13–19/IV/2004, H. Höfer <i>et al</i>. col. (IBSP 143796; MCN 44720); Guaraqueçaba, Reserva Natural da Serra do Itaqui, (25°18'25''S; 48°19'44''W), 3Ψ, IX/2007, L. Scheuermann <i>et al</i>. col. (IBSP 143750; IBSP 143799). <b>Santa Catarina:</b> Paulo Lopes, Parque Estadual da Serra do Tabuleiro, (27°52'14"S; 48°47'10"W), 1Ψ, 10–20/II/2002, Equipe Biota col. (IBSP 143792). <b>Rio de Janeiro:</b> Teresópolis, Parque Nacional da Serra dos Órgãos, (22º24'43''S; 42º57'57''W), 1Ψ, 23/VIII/2001, Equipe Biota col. (IBSP 132172). <b>São Paulo:</b> Peruíbe, Estação Ecológica da Juréia-Itatins, (24º33'S; 47º13'W), 1ɗ1Ψ, 26/IV–3/V/1999, A. D. Brescovit <i>et al</i>. col. (IBSP 25251; IBSP 24852).</p>Published as part of <i>Lemos, Yuji & Brescovit, Antonio D., 2013, New species of the spider genus Exocora Millidge, 1991 (Araneae: Linyphiidae) from Brazil, pp. 261-278 in Zootaxa 3599 (3)</i> on page 266, DOI: 10.11646/zootaxa.3599.3.4, <a href="http://zenodo.org/record/224180">http://zenodo.org/record/224180</a>
Exocora ribeiroi Lemos & Brescovit, 2013, new species
No full textExocora ribeiroi new species Figs 6 A–D; 7 A–F; 15 C; 16 C; 17 Types: Holotype 1 ɗ, from Estação Biológica Costão da Serra (28 º 66 ' 19 ''S, 49 º 62 ' 37 ''W), Siderópolis, Santa Catarina, Brazil, 1 /VII/ 2006, R. A. Teixeira et al. col. (IBSP 84839). Paratype: 1 Ψ, from Rio Molha (28 º 31 'S; 49 º 19 'W), Urussanga, Santa Catarina, Brazil, 23 /X/ 2006 – 25 /I/ 2007, R. Teixeira col. (IBSP 129743); 2 ɗ 4 Ψ, from Centro de Pesquisas e Conservação da Natureza Pró-Mata (29 ° 26 'S; 50 ° 35 'W), São Francisco de Paula, Rio Grande do Sul, Brazil, 18 /V/ 2002, R. Ott col. (MCN 39413), 1 ɗ 1 Ψ, 2 /I/ 2001, R. Ott col. (MCN 39414). Etymology: The species name is in memory of Jair Aparecido Ribeiro, a great friend, who fought cancer until his last day. The name is a noun in genitive. Diagnosis: Specimens of Exocora ribeiroi n. sp. resemble those of E. girotii n. sp., differing in the shape of the anterior part of lamella characteristica, which is straight and curved dorsally (Figs 6 A, B). Females of E. ribeiroi n. sp. can be diagnosed by the opening of the atrium, wider in E. girotii n. sp., and by the distance between the copulatory ducts, which are more separated than in the other species in the genus (Figs 6 C, D; 15 C; 16 C). Description: Male (Holotype IBSP 84839): Total length 1.92. Carapace 0.88 long, 0.72 wide; orange with dark lateral markings. Sternum 0.46 long, 0.5 wide, orange with darkened margins. Clypeus 0.16 high. Chelicerae promargin with 3 teeth, retromargin with 3 teeth. Abdomen pale brown with strong dark markings along the entire surface (Figs 7 A, B). Eyes diameter and interdistances: AME 0.06, ALE 0.1, PME 0.08, PLE 0.1, AME-AME 0.02, PME-PME 0.02, AME-ALE 0.03, PME-PLE 0.03. Eyes projected. Bristles present in ocular area (Fig. 7 B). Coxa IV separation 1.14 times their width. Femur I/II/III/IV 0.94 / 0.86 / 0.6 / 0.8; patella I 0.3; tibia I 0.92; metatarsus I 0.92; tarsus I 0.54. Legs orange with darkened markings on each articles. Tibia I prolateral macroseta thick and curved (Fig. 7 C). TmI 0.22. Palpal tibia without apophysis. Protegulum present. Radix small. Embolus long, filiform, with origin at the posterior part of the embolic division, runs to the ectal side curving several times. Embolic membrane small (Figs 6 A, B). Female (Paratype IBSP 129743): Total length 1.8. Carapace 0.82 long, 0.66 wide. Sternum 0.46 long, 0.46 wide. Clypeus 0.1 high. Chelicerae promargin with 3 teeth, retromargin with 5 teeth. Body color pattern same as male (Figs 7 D, E). Eyes diameter and interdistances: AME 0.06, ALE 0.09, PME 0.09, PLE 0.08, AME-AME 0.02, PME-PME 0.02, AME-ALE 0.03, PME-PLE 0.03. Eyes as observed in males, but with less bristles in ocular area (Fig. 7 E). Coxa IV separation 1.16 times their width. Femur I/II/III/IV 0.8 / 0.76 / 0.58 / 0.74; patella I 0.26; tibia I 0.74; metatarsus I 0.74; tarsus I 0.46. Legs pattern same as male, tibia I prolateral macroseta straighter (Fig. 7 F). TmI 0.22. Epigynum ventral plate prominent (Figs 6 C; 15 C). Spermathecae oblong. Copulatory ducts long and coiled, with its origin in the ventral part of the spermathecae. Fertilization duct originating from the dorsal part of the spermatheca, running ectally (Figs 6 D; 16 C). Variation: Males (n= 5): Total length 1.72–2.06; carapace length 0.92–1.02; carapace width 0.78–0.88; femur I length 1.0– 1.1. Females (n= 10): Total length 1.68–2.08; carapace length 0.8–0.88; carapace width 0.66–0.76; femur I length 0.76–0.88. Distribution: States of São Paulo, Santa Catarina, Rio Grande do Sul, in Brazil (Fig. 17). Material examined (N= 17): BRAZIL, São Paulo: São José do Barreiro, Parque Nacional da Serra da Bocaina (22 º 43 'S; 44 º 36 'W), 1 ɗ, 28 /IV– 3 /V/ 2002, Equipe Biota col. (IBSP 60020); Santa Catarina: Campo Belo do Sul (27 ° 53 ' 56 ''S; 50 ° 45 ' 39 ''W), 1 Ψ, 23–27 /XI/ 2007, T. G. Pinto col. (MCN 4207); Rio Grande do Sul: São Francisco de Paula, Centro de Pesquisas e Conservação da Natureza Pró-Mata (29 ° 26 'S; 50 ° 35 'W), 4 ɗ 11 Ψ, 4 /IX/ 2001, R. Ott col. (MCN 39409 -39410; 39412; 39415; 39417).Published as part of Lemos, Yuji & Brescovit, Antonio D., 2013, New species of the spider genus Exocora Millidge, 1991 (Araneae: Linyphiidae) from Brazil, pp. 261-278 in Zootaxa 3599 (3) on page 268, DOI: 10.11646/zootaxa.3599.3.4, http://zenodo.org/record/22418
Dolops carvalhoi Lemos de Castro 1949
No full textDolops carvalhoi Lemos de Castro, 1949 (Figure 10) D. carvalhoi: LEMOS DE CASTRO (1949): 4–6, fIGS. 9–20, 23–25; Dolops geayi BOUVIER, 1897: IN PART WEIbEZAHN & CObO (1964): 123, PL. I–II; D. carvalhoi: LEMOS DE CASTRO (1985): 12, 57–59; THATcHER (2006): 394, 396, 399. Type host. Rhaphiodon vulpinus Agassiz, 1829 (Lemos de Castro 1949) Type locality. Confluence between Kuluene and Xingu Rivers, state of Mato Grosso, Brasil (Lemos de Castro 1949) Other hosts and localities. R. vulpinus, C. macropomum, the clupeiform Pellona castelnaeana Valenciennes, 1847, P. fasciatum, P. tigrinum, Phractocephalus hemiliopterus (Bloch & Schneider, 1801), Janauacá Lake, state of Amazonas, Brazil (Malta & Varella 1983); P. nattereri, Serrasalmus spilopleura Kner, 1858, S. marginatus, Brazilian Pantanal wetland, state of Mato Grosso do Sul, Brazil (Carvalho et al. 2003); P. nattereri, Araguaia River Basin, state of Goiás, Brazil (Carvalho et al. 2004); P. fasciatum (Linnaeus, 1766), P. tigrinum, Ichilo River, Bolivia (Mamani et al. 2004). Material deposited. 10 vouchers: 1 adult male ZUEC-CRU 3505, 4 July 2008, 1 adult female ZUEC-CRU 3506, 1 adult female INPA 2312, 8 July 2008, 1 adult male ZUEC-CRU 3503, 1 adult female MZUSP 36232, 8 July 2009, in ethanol 70%, Pseudoplatystoma corruscans, skin; 1 adult female ZUEC-CRU 3502, 1 adult female INPA 2313, in ethanol 70%, 8 July 2009, Pseudoplatystoma reticulatum, skin; 1 adult female ZUEC-CRU 3507, in ethanol 70%, 8 July 2008, Zungaro zungaro, skin; 1 immature female INPA 2314, in Hoyer’s medium, 1 immature female ZUEC-CRU 3404, 8 July 2009, skin, Salminus brasiliensis; all from Cuiabá River, Parque Nacional do Pantanal Matogrossense, Mato Grosso, Brazil (17°49′37.77″ S, 57°22′53.38”W). Measurements. Based on 3 males and 8 females. Total length (mm) 5.2 (4.2–6.1, n = 2) in males, 7.4 (5–11.1) in females. Carapace length 3.4 (2.7–4.1, n = 2) in males, 5.1 (3.6–7.7) in females; maximum carapace width 4.6 (3.2–6, n = 2) in males, 6 (4.3–8.5) in females. Carapace posterior sinus length 1 (0.7–1.2; n = 2) in males, 1.7 (1– 2.5) in females; width 1.2 (0.9–1.6, n = 2) in males, 2 (1.5–3) in females. Cephalothorax length 2 (1.5–2.9) in males, 3.2 (1.4–5.2) in females; anterior width 2 (1.6–2.5) in males, 3.5 (2.3–7) in females. Abdomen length 2.3 (1.5–3.1, n = 2) in males, 2.1 (1.5–2.9) in females; width 1.2 (1.1–1.3, n = 2) in males, 1.8 (1.3–2.4) in females. Abdomen posterior sinus length 1.9 (0.9–2.8, n = 2) in males, 1.4 (0.8–2) in females; width 0.8 (0.3–1.25, n = 2) in males, 0.7 (0.15–1). Eyes diameter (µm) 225 left and 200 right in one male, 336 (250–450, n = 7), left 332 (250– 425, n = 7) right in female; transverse distance between eyes (µm) 725 in one male, 1461 (1050–2000, n = 7) in female. First maxillae length 1.1 (0.8–1.4) left and 1.1 (0.7–1.5) right in males, 1.1 (0.7––1.7) left and 1 (0.7–1.6) right in females; Hook of the first maxillae length (µm) 715 (413–1250) left and 725 (431–1300) right in males, 498 (263–658) left and 452 (273–712.5) in females. Seta-like structure length (µm) 186 (140–250) left and 205 (114–275) right in males, 194 (75–250, n = 7) left and 160 (76.5–310, n = 7) right in females. Remarks. The specimens of D. carvalhoi that we observed had a pyriform carapace, which was wider than it was long, and, more frequently, covered all the legs in both males and females. There are no spines on the ventral surface of the carapace of this species (Lemos de Castro 1949) and the testis are bilobate. The presence of these characteristics makes its morphological relationship with D. longicauda, D. geayi and D. nana Lemos de Castro, 1950 (Bouvier 1899; Heller 1857; Lemos de Castro 1950) narrower. In his description of D. nana, Lemos de Castro (1950) stated that there are two spines plus a lobe on the base of the second maxillae. The author also exhibited legs without flagella in his drawings. Nevertheless, specimens of D. carvalhoi, D. longicauda and D. geayi have three spines on the base of the second maxillae (Fig. 10D) and flagella in at least the first and second legs. Males and females of D. carvalhoi have flagella on the first three legs (Lemos de Castro 1949). This, distinguishes them from specimens of D. geayi, which have flagella on just the first two pairs of legs (Bouvier 1899; Ringuelet 1943). Lemos de Castro (1949) said that the second pairs of flagella of D. carvalhoi are the largest and the third pairs smaller. However, in his drawings, he showed the first pair of flagella as smaller. In the specimens examined in the present study, we saw that only males exhibited smaller flagella on the third legs, whereas in D. longicauda, both males and females exhibited smaller flagella on the third legs. The spines on the base of the second maxillae are similar in D. carvalhoi and D. longicauda. The morphology of the anal papillae of the female (Fig. 10B, 11F) is also similar for these two species. Furthermore, a seta-like structure on the hook of the second maxillae without spines is present in both species (Fig. 10C, 11E). Morphologically speaking, therefore, the color pattern (bluish or greenish in D. longicauda, brownish in D. carvalhoi); the flagella on the third legs of females; and especially the abdomen length (smaller in D. carvalhoi: 27% and 44%, of female and male total length, respectively; larger in D. longicauda: 64% of total length) are important characteristics for distinguishing D. carvalhoi from D. longicauda. Yet, there are four to six multi-digit scales on the mandibles of D. carvalhoi, many of which are present on the legs (Fig. 10A), while in D. longicauda there are no scales on any part of it body.Published as part of Tavares, Luiz E. R., 2017, A new species of Argulus (Crustacea, Branchiura, Argulidae) from the skin of catfish, with new records of branchiurans from wild fish in the Brazilian Pantanal wetland, pp. 447-469 in Zootaxa 4320 (3) on pages 462-464, DOI: 10.11646/zootaxa.4320.3.3, http://zenodo.org/record/89375
FIGURE 6. Exocora ribeiroi n in New species of the spider genus Exocora Millidge, 1991 (Araneae: Linyphiidae) from Brazil
No full textFIGURE 6. Exocora ribeiroi n. sp., male palp (A, B), epigynum (C, D): A, retrolateral; B, prolateral; C, ventral; D, dorsal. Scale bars 0.1mm.Published as part of Lemos, Yuji & Brescovit, Antonio D., 2013, New species of the spider genus Exocora Millidge, 1991 (Araneae: Linyphiidae) from Brazil, pp. 261-278 in Zootaxa 3599 (3) on page 269, DOI: 10.11646/zootaxa.3599.3.4, http://zenodo.org/record/22418
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