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FIGURE 18. A–C in Two new species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) from Brazilian caves
FIGURE 18. A–C, Xangoniscus aganju Campos-Filho, Araujo & Taiti, 2014 (photos: P.P. Rizzato and M.E. Bichuette); D, Benthana xiquinhoi Campos-Filho, Bichuette & Taiti sp. n. (photo: J.E. Gallão).Published as part of Campos-Filho, Ivanklin Soares, Fernandes, Camile Sorbo, Cardoso, Giovanna Monticelli, Bichuette, Maria Elina, Aguiar, José Otávio & Taiti, Stefano, 2019, Two new species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) from Brazilian caves, pp. 422-448 in Zootaxa 4564 (2) on page 443, DOI: 10.11646/zootaxa.4564.2.6, http://zenodo.org/record/258928
Álgebras aproximadamente finitas /
Dissertação (Mestrado) - Universidade Federal de Santa Catarina, Centro de Ciências Físicas e Matemáticas
O filho ilegítimo de Antonio Manoel Victorino de Menezes, traficante de escravos, com a escrava parda Maria Margarida Duarte.
TCC (graduação) - Universidade Federal de Santa Catarina - Centro de Filosofia e Ciências Humanas, Departamento de História.No presente trabalho analiso o envolvimento entre um traficante de escravos de Desterro (SC), com uma de suas cativas e o filho, fruto dessa relação. Com isso, viso discutir sobre o espaço destinado aos filhos ilegítimos durante século XIX, processo de tutela e possível ascensão social de crianças que tiveram sua vida afastada, de alguma maneira, dos estigmas da escravidão e da ilegitimidade, aspectos estes bastante excludentes para aquela sociedade patriarcal e escravista
Fig. 8 in New species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) of the families Philosciidae and Scleropactidae from Brazilian caves
Fig. 8. Metaprosekia igatuensis Campos-Filho, Fernandes & Bichuette sp. nov., ♀, paratype (LES 6349). A. Habitus, dorsal view. B. Dorsal scale-seta. C. Pereonite 1 epimeron, dorsal view. D. Noduli laterales d/c coordinates. E. Noduli laterales b/c coordinates. F. Cephalon, frontal view. G. Pleonites 4–5 and telson. H. Antennula. I. Antenna.Published as part of <i>Campos-Filho, Ivanklin Soares, Fernandes, Camile Sorbo, Cardoso, Giovanna Monticelli, Bichuette, Maria Elina, Aguiar, José Otávio & Taiti, Stefano, 2020, New species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) of the families Philosciidae and Scleropactidae from Brazilian caves, pp. 1-38 in European Journal of Taxonomy 606</i> on page 20, DOI: 10.5852/ejt.2020.606, <a href="http://zenodo.org/record/10075119">http://zenodo.org/record/10075119</a>
FIGURE 6. Cylindroniscus platoi n in Cylindroniscus platoi (Isopoda: Oniscidea: Styloniscidae), a new cave-dwelling species from Lagoa Santa Karst, Southeastern Brazil
FIGURE 6. Cylindroniscus platoi n. sp. A. gEniTaL PaPiLLa; B. PLEOPOd 1; C. PLEOPOd 2 EndOPOd; D. PLEOPOd 3 EXOPOd; E. PLEOPOd 4 EXOPOd; F. PLEOPOd 5 EXOPOd.Published as part of Fernandes, Camile Sorbo, Campos-Filho, Ivanklin Soares & Bichuette, Maria Elina, 2018, Cylindroniscus platoi (Isopoda: Oniscidea: Styloniscidae), a new cave-dwelling species from Lagoa Santa Karst, Southeastern Brazil, pp. 411-420 in Zootaxa 4461 (3) on page 418, DOI: 10.11646/zootaxa.4461.3.6, http://zenodo.org/record/146017
Fig. 9 in New species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) of the families Philosciidae and Scleropactidae from Brazilian caves
Fig. 9. Metaprosekia igatuensis Campos-Filho, Fernandes & Bichuette sp. nov., ♀, paratype (LES 6349). A. Left mandible. B. Right mandible. C. Maxillula. D. Maxilla. E. Maxilliped.Published as part of <i>Campos-Filho, Ivanklin Soares, Fernandes, Camile Sorbo, Cardoso, Giovanna Monticelli, Bichuette, Maria Elina, Aguiar, José Otávio & Taiti, Stefano, 2020, New species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) of the families Philosciidae and Scleropactidae from Brazilian caves, pp. 1-38 in European Journal of Taxonomy 606</i> on page 21, DOI: 10.5852/ejt.2020.606, <a href="http://zenodo.org/record/10075119">http://zenodo.org/record/10075119</a>
Alboscia jotajota Campos-Filho & Fernandes & Cardoso & Bichuette & Aguiar & Taiti 2020, sp. nov.
Albosciajotajota Campos-Filho, Bichuette & Taiti sp. nov. urn:lsid:zoobank.org:act: 872601F5-076C-44FD-83E7-0FC35123E54D Figs 2–4, 14 Diagnosis Eyes reduced to rudimentary ommatidia, distal article of antennula with six lateral aesthetascs plus apical pair and male pleopod 1 endopod slightly longer than exopod, with short and thickset distal portion. Etymology This new species is named after Joaquim Justino dos Santos (in memoriam), also known as ʻJota Jotaʼ, who discovered several caves in the Alto Ribeira karst area and was a fantastic guide at PETAR. Material examined Holotype BRAZIL – São Paulo State, Iporanga • ♂; PEI, Gruta Minotauro; 24°16′34″ S, 48°27′22″ W; 26–30 Mar. 2009, F. Pellegatti-Franco leg.; parts in micropreparations; LES 647. Paratypes BRAZIL – São Paulo State, Iporanga • 2 ♀♀; PETAR, Ressurgência das Areias de Água Quente Cave; 24°33′45″ S, 48°40′18″ W; 29 Sep. 2012; M.E. Bichuette leg.; LES 18852. Description MEASUREMENTS. Maximum body length: male 4 mm, female 4.5 mm. BODY. Body pigments absent. Body (Fig. 2A) slender with lateral sides almost parallel; dorsal surface smooth, bearing short, triangular scale-setae (Fig. 2B). Noduli laterales very long (Fig. 2C); d/c and b/c coordinates as in Fig. 2 D–E. CEPHALON. Lateral lobes not developed, frontal line absent, suprantennal line slightly bent downwards in middle; eyes reduced, with rudimentary ommatidia (Fig. 2F). PEREON. Pereonite 1 epimera with anterior corners slightly directed upwards, not surpassing median portion of cephalon, epimera 2–7 gradually directed backwards (Fig. 2A). PLEON. Narrower than pereon; pleonites 3–5 epimera short, adpressedwith small posterior points directed backwards, bearing some glandular pores; telson triangular with lateral margins straight, rounded apex (Fig. 2G). ANTENNULA. Composed of three articles, distal article bearing six lateral aesthetascs in three sets plus apical pair (Fig. 2H). ANTENNA. Very long, reaching fourth pereonite when extended backwards; flagellum of three articles, distal article longest; apical organ short, bearing two long free sensilla (Fig. 2I). MOUTH. Mandibles bearing dense cushion of setae on incisor process, molar penicil consisting of several branches; right mandible (Fig. 3A) with 1+1 penicils, left mandible (Fig. 3B) with 2+1 penicils. Maxillula (Fig. 3C) inner endite with distal margin rounded and bearing two penicils; outer endite with four simple teeth plus accessory tooth on outer set, inner set of five pectinate teeth plus one vestigial tooth on rostral surface. Maxilla (Fig. 3D) inner lobe rounded, covered with thick and thin setae; outer lobe slightly wider than inner lobe, covered with thin setae. Maxilliped (Fig. 3E) palp with two strong setae on proximal article; endite subrectangular, medial seta strong, surpassing distal margin, distal margin with two hook-like setae, rostral surface with setose sulcus ending in one strong, triangular seta. PEREOPODS. Pereopods 1–7 merus to propodus bearing sparse, long setae on sternal margin; pereopod 1 carpus with transverse antennal grooming brush; dactylus of two claws, inner claw not surpassing outer claw, dactylar and ungual setae simple, not surpassing outer claw. UROPOD. Protopod subquadrangular with endopod and exopod inserted at same level; protopod and exopod outer margins grooved, bearing glandular pores; exopod slightly longer than endopod (Fig. 4A). PLEOPOD EXOPODS. Without respiratory structures (Fig. 4E–I). Male PEREOPODS 1 AND 7. Without any sexual dimorphism (Fig. 4B–C). GENITAL PAPILLA. Stout, with triangular ventral shield, papilla slightly longer than ventral shield, bearing two apical orifices (Fig. 4D). PLEOPODS. Pleopod 1 (Fig. 4E) exopod subcircular, wider than long; endopod short and stout, with distal portion thickset and slightly bent outwards, rounded apex. Pleopod 2 (Fig. 4F) exopod triangular, outer margin almost straight, bearing one seta, distal margin rounded; endopod longer than exopod. Exopods of pleopod 3 and 4 subrectangular, outer margin almost straight and bearing three long setae (Fig. 4 G– H). Pleopod 5 exopod (Fig. 4I) triangular, outer margin convex, bearing three long setae, distal margin rounded. Remarks To date, the genus Alboscia comprises four species: A. elongata Schultz, 1995 from Paraguay; A. itaipuensis Araujo & Quadros, 2005, A. ornata Araujo, 1999 and A. silveirensis Araujo, 1999 from Brazil (Schultz 1995; Araujo 1999; Araujo & Quadros 2005). The genus is mainly defined by the slender habitus with lateral sides almost parallel, presence of conspicuous noduli laterales, epimera of pleonites closely appressed to pleon, maxillula outer endite with pectinate teeth on outer set and pleopod exopods without respiratory structures (Araujo 1999). The presence of pectinate teeth on the outer endite of the maxillula is present in other lineages of Oniscidea, e.g., Ligia Fabricius, 1798 (Ligiidae Leach, 1814), Armadilloniscus Uljanin, 1875 (Detonidae Budde-Lund, 1906)), Benthana Budde-Lund, 1904, Benthanops Barnard, 1932 and Ctenoscia Verhoeff, 1928 (Philosciidae), and Rhyscotidae Budde-Lund, 1908 (see Taiti & Ferrara 1982; Leistikow 1997; Schmidt 2002, 2003; Campos-Filho et al. 2015a). This character state is considered to be plesiomorphic (Leistikow 2001; Schmidt 2002). In the shape of the male pleopod 1 exopod, Alboscia jotajota sp. nov. resembles A. elongata and A. silveirensis. It differs from both species in having eyes with rudimentary ommatidia (vs three ommatidia in A. elongata; single ommatidium in A. silveirensis), antennula with six lateral aesthetascs arranged in three sets (vs five in one set in A. elongata; two in one set in A. silveirensis) and the male pleopod 1 endopod slightly longer than the exopod, with short and thickset distal portion (vs more than twice as long as exopod and distal portion slender in A. elongata; three times as long as exopod and distal portion slender in A. silveirensis). The absence of body pigment and absent/reduced eyes are common to all species of Alboscia, which probably indicates an endogean way of life. However, Alboscia jotajota sp. nov. is considered to be troglobiotic since no specimen was collected during surveys outside the caves where this species occurs.Published as part of Campos-Filho, Ivanklin Soares, Fernandes, Camile Sorbo, Cardoso, Giovanna Monticelli, Bichuette, Maria Elina, Aguiar, José Otávio & Taiti, Stefano, 2020, New species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) of the families Philosciidae and Scleropactidae from Brazilian caves, pp. 1-38 in European Journal of Taxonomy 606 on pages 6-11, DOI: 10.5852/ejt.2020.606, http://zenodo.org/record/367698
Xangoniscus aganju Campos-Filho, Araujo & Taiti 2014
Xangoniscus aganju Campos-Filho, Araujo & Taiti, 2014 Figs 7, 17b, 18 A–C Styloniscidae indet. 3 Gallão & Bichuette, 2018: 12, table 2. Styloniscidae indet. 4 Gallão & Bichuette, 2018: 12, table 2. Material examined. Bahia: 1 male, 5 females (LES 6437), Carinhanha, Serra do Ramalho karst area, Caverna Domingão, 13°44’41”S, 43°50’00”W, 27 July 2012, leg. M.E. Bichuette, J. E. Gallão and P. P. Rizzato; 4 males (LES 14351), 1 female (LES 6435), Coribe, Serra do Ramalho karst area, Caverna Chico Pernambuco, 13°49’10”S, 44°04’15”W, 28 July 2012, leg. M.E. Bichuette, J. E. Gallão, L. Senna-Horta and P.P. Rizzato. Remarks. To date, the genus Xangoniscus comprises three troglobiotic species with amphibious life-style, all endemic to Brazilian caves: Xangoniscus aganju, X. odara, and X. itacarambiensis. The genus is mainly defined by the complex wrench-like distal portion of the male pleopod 2 endopod, unique among the Styloniscidae (see Campos-Filho et al. 2014, 2016; Bastos-Pereira et al. 2017). The specimens from the two caves in the Bahia state here examined are tentatively identified as X. aganju since they show the same morphological characters. Only small differences are present in the apical lobes of the male pleopod 2 endopod (compare fig. 13C in Campos-Filho et al. (2014) with Fig. 7A, B, specimens from Caverna Chico Pernambuco, and Fig. 7C, specimens from Caverna Domingão). A molecular analysis of all the populations of X. aganju may clarify if these small differences indicate distinct taxa. The Chico Pernambuco and the Caverna Domingão caves are located in the Serra do Ramalho karst area, state of Bahia, northeastern Brazil. The caves are not legally protected and their surroundings are used for agriculture, pasture and projects for mining activities (Fig. 2A, B). The population of X. aganju from Chico Pernambuco is abundant in part of the drainage (level base stream) of the cave, reaching 8–10 inds/m 2 and showing gregarious habitus (Fig. 18B). The population from Caverna Domingão occurs in a phreatic habitat, a relatively large pool in the distal part of the cave with a high abundance, reaching 20 inds/m 2, preferring submersed organic matter (mainly trunks) and showing gregarious habits (Fig. 18C).Published as part of Campos-Filho, Ivanklin Soares, Fernandes, Camile Sorbo, Cardoso, Giovanna Monticelli, Bichuette, Maria Elina, Aguiar, José Otávio & Taiti, Stefano, 2019, Two new species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) from Brazilian caves, pp. 422-448 in Zootaxa 4564 (2) on pages 429-430, DOI: 10.11646/zootaxa.4564.2.6, http://zenodo.org/record/258928
Benthana xiquinhoi Campos-Filho & Fernandes & Cardoso & Bichuette & Aguiar & Taiti 2019, sp. n.
Benthana xiquinhoi Campos-Filho, Bichuette & Taiti sp. n. Figs 11–13, 18D Zoobank. urn:lsid:zoobank.org:act: F4730822-4853-4CE3-8F20-0C5E9DD0D7F3. Philosciidae indet 2 Gallão & Bichuette, 2018: 12, table 2. Etymology. The new species is named after Raimundo Cruz do Santos, also called ‘Xiquinho’, for his great contribution to cave surveys and his enthusiasm for cave fauna and discoveries. Material examined. Holotype Bahia, Andaraí, Povoado de Igatu: male (LES 6353), Gruna Parede Vermelha cave, 12°52’41”S, 41°18’57”W, 2 April 2013, leg. M.E. Bichuette, J.E. Gallão and D.M. von Schimonsky. Paratypes: 2 males (LES 6352) (parts in micropreparations), same data as holotype; 1 female (LES 6335), same locality, 31 May 2010, leg. M.E. Bichuette, B. Rantin, J.E. Gallão and L. B. Simões; 1 female (parts in micropreparations) (LES 6337), same locality, 29 October 2010, leg. M.E. Bichuette and J. E. Gallão; 1 female (LES 6342), Gruna Veio de Aurélio cave, 12°51’36”S, 41°18’11”W, 28 October 2010, leg. M.E. Bichuette and J. E. Gallão; 2 females, 1 juvenile (LES 6348), Gruna Lava Pé cave, 12°53’42”S, 41°19’04”W, 30 March 2013, leg. M.E. Bichuette, J. E. Gallão and D.M. von Schimonsky. Description. Maximum body length: male 9.5 mm, female 10.5 mm. Colour light brown: cephalon with irregular unpigmented spots; pereonites 1–7 weakly pigmented on medial portion, epimera more pigmented; pleonites 1–5 with unpigmented spots on medial portion, pleonites 3–5 more pigmented on paramedian and median portions; telson pigmented. Body convex, outline as in Fig. 11A. Dorsal surface smooth bearing few long triangular scale-setae (Fig. 11B). Noduli laterales long, one line per side with d/c coordinates reaching a maximum on pereonite 4; b/c coordinates gradually decreasing (Fig. 11C, D). Cephalon (Fig. 11E) with suprantennal line bent downwards in middle, no frontal line and lateral lobes; eyes composed of 10–12 small ommatidia arranged in four rows. Pereonites 1–4 with postero-lateral corners right-angled with rounded apices and posterior margins straight; pereonites 5–7 with postero-lateral corners gradually more acute and posterior margins gradually more arched. Pleon narrower than pereon, pleonites 3–5 with epimera triangular, acute, and directed backwards (Fig. 11A). Telson (Fig. 11F) triangular, lateral sides straight and apex broadly rounded. Antennula (Fig. 11G) of three articles, distal article longest bearing seven lateral aesthetascs plus apical pair. Antenna (Fig. 11H) very long, reaching pereonite 4 when extended backwards, distal article of peduncle longer than flagellum; flagellum of three articles, proximal article longest, apical organ short bearing two long sensilla. Mandibles with molar penicil of eight branches and dense cushion of setae, left mandible (Fig. 12A) with 2+1 penicils, and right mandible (Fig. 12B) with 1+1 penicils. Maxillula (Fig. 12C) outer endite with two penicils, distal margin rounded; outer endite with 4+6 teeth, five of them pectinate, one short and simple. Maxilla (Fig. 12D) outer lobe twice as wide as inner lobe with distal margin sinuous, covered with thin setae; inner lobe rounded covered with thick setae. Maxilliped (Fig. 12E) with rectangular basis with sparse setae; endite rectangular, distal margin slightly sinuous, medial seta surpassing distal margin, two hooks on distal margin, longitudinal ridge bearing dense setae ending with one short triangular seta; proximal article of palp with two stout setae. Pereopods rather slender, bearing distal fringe of hyaline scales on merus and carpus; carpus 1 with transverse antenna-grooming brush and distal seta with hand-like apex; dactylus with inner claw reaching distal margin of outer claw, dactylar and ungual setae simple, not surpassing outer claw. Uropod (Fig. 13A) protopod subquadrangular, protopod and exopod grooved on outer margin bearing glandular pores, exopod twice as long as endopod, endopod inserted proximally. Pleopod exopods with Benthana - type respiratory areas. Male. Pereopods 1–3 (Fig. 13B) merus and carpus with brushes of setae on sternal margin. Pereopod 7 (Fig. 13C) without sexual dimorphism. Genital papilla (Fig. 13D) with triangular ventral shield and two subapical orifices. Pleopod 1 (Fig. 13E) exopod heart-shaped, elongated (ratio z:y= 2.15), lateral protrusion prominent with acute apex, distal margin straight; endopod longer than exopod, stout and straight, distal portion with line of short setae. Pleopod 2 (Fig. 13F) exopod triangular, outer margin concave with two setae; endopod slender, distinctly longer than exopod. Pleopods 3 and 4 exopods as in Fig. 13G and H, respectively. Pleopod 5 exopod (Fig. 13I) triangular, outer margin almost straight with five setae. Remarks. The genus Benthana comprises 28 species mainly distributed in the Atlantic Forest areas of Brazil, with Benthana picta (Brandt, 1833) occurring also in Paraguay (Campos-Filho et al. 2015). Only two species were previously recorded from cave habitats, the troglobiont B. iporangensis Lima & Serejo, 1993 from Ressurgência das Areias de Água Quente and Areias de Cima caves (Areias system), and Gruta do Tatu cave, all included in conservation units in the state of São Paulo, and the non-troglomorphic and probably trogloxene B. taeniata Araujo & Buckup, 1994 from Gruta Zeferino I, state of Minas Gerais (Campos-Filho et al. 2014, 2015). Those caves are located in Chapada Diamantina region at the boundaires of Caatinga vegetation and surrounded by remains of the Atlantic forest and “campos rupestres” vegetation, a variation of Cerrado, not as dry as Caatinga (Fig. 2C, D). The new species occurs in very humid sandy (unconsolidated) or rocky substrate with organic matter (mainly moss close to creeks inside caves), showing medium abundance and densities (lower <0.5 inds/m 2) (Fig. 18D). The new species is considered to be troglobiotic. Benthana xiquinhoi sp. n. is similar to B. picta in the shape of the male pleopod 1 exopod; it is readily distinct in the reduced number of ommatidia, 10–12 (vs. 24 in B. picta), telson with distal margin rounded (vs. triangular), mandibles with eight branches on molar penicil (vs. 12), uropod exopod longer than endopod (vs. subequal), male pleopod 1 endopod straight (vs. bent outward s). Only Benthana schubarti Lemos de Castro, 1958 and B. iporangensis show eyes with reduced number of ommatidia, 16 and 18, respectively; Benthana xiquinhoi sp. n. distinctly differs from those species in the shape of the male pleopod 1 exopod (see Campos-Filho et al. 2015).Published as part of Campos-Filho, Ivanklin Soares, Fernandes, Camile Sorbo, Cardoso, Giovanna Monticelli, Bichuette, Maria Elina, Aguiar, José Otávio & Taiti, Stefano, 2019, Two new species and new records of terrestrial isopods (Crustacea, Isopoda, Oniscidea) from Brazilian caves, pp. 422-448 in Zootaxa 4564 (2) on pages 434-438, DOI: 10.11646/zootaxa.4564.2.6, http://zenodo.org/record/258928
FIGURE 5 in Termitaphididae, a family of true bugs (Heteroptera) new to Brazil, with the redescription of Termitaradus trinidadensis
FIGURE 5. Male and female terminalia of Termitaradus trinidadensis (Morrison, 1923). A. Male terminalia. B. Male terminalia. C. Spermatheca, ventral view. Scale bars: 200 μm. Abbreviations: aed = aedeagus; ejr = ejaculatory reservoir; lb = lobule; lm = lamina; osd = outgrowth of the spermathecal duct; phb = phallobase; par = paramere; pr = pumping region; pyg = pygophore; sb = spermathecal bulb; sd, spermathecal duct.Published as part of Carvalho-Filho, Fernando Da Silva & Fernandes, José Antônio Marin, 2020, Termitaphididae, a family of true bugs (Heteroptera) new to Brazil, with the redescription of Termitaradus trinidadensis, pp. 425-433 in Zootaxa 4822 (3) on page 431, DOI: 10.11646/zootaxa.4822.3.7, http://zenodo.org/record/440176
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