71,995 research outputs found
Chnoodes unimaculata Krüger, Castro-Guedes & Almeida, 2016, sp. nov.
No full textChnoodes unimaculata sp. nov. (Figure 8) Material examined. BRAZIL: Amapá: “Oiapoque/Amapá - Brasil / V. 1959 /M. Alvarenga col.”, “Ex-Coleção/M. Alvarenga”, [DZUP 188165] “ HOLOTYPE [female]/ Chnoodes unimaculata Krüger, Castro-Guedes & Almeida, 2015 ” [red label]; “ Brasil - Amapá/Macapá/ 16.III. 2004 /J. F. F. Martins, [DZUP 186838] “ PARATYPE [female]/ Chnoodes unimaculata Krüger, Castro-Guedes & Almeida, 2015 ” [yellow label]. Holotype. Female. Length 3.16 mm, width 2.40 mm. Body round, with sparse yellowish pubescence. Pronotum black, with yellowish lateral border. Elytra black with one elongated yellowish spot on disc (Figs 8 A–D). Head, antennae and mouthparts dark yellowish. Meso- and metasternum dark brown or black; legs yellowish; epipleuron with black spots; first ventrites black (Fig. 8 B). Genitalia with genital plates triangular, elongated, styli with setae (Fig. 8 E). Spermatheca C-shaped, apex short and rounded (Fig. 8 F). Male. Unknown. Etymology. The name of this species refers to the single spot on each elytron. Geographical Distribution. Brazil (AP). Remarks. Chnoodes unimaculata sp. nov. (Fig. 8) resembles C. machadoi sp. nov. (Fig. 7), but is clearly distinguished by the color, shape and number of spots on the elytra; it also differs in the shape of the female genitalia.Published as part of Krüger, Thaysa C., Castro-Guedes, Camila F. & Almeida, Lúcia M., 2016, Two new species of Chnoodes Chevrolat (Coleoptera: Coccinellidae) from Brazil, pp. 269-283 in Zootaxa 4078 (1) on pages 281-282, DOI: 10.11646/zootaxa.4078.1.24, http://zenodo.org/record/26066
Reptadeonella brasiliensis ALMEIDA, SOUZA, SANNER & VIEIRA 2015
No full textReptadeonella brasiliensis Almeida, Souza, Sanner & Vieira, 2015 (Fig. 3E, F; Table 4) Reptadeonella brasiliensis ALMEIDA, SOUZA, SANNER & VIEIRA, 2015: P. 357, fIgS 19–28, 39, 40 (CUM SYN.). Material examined. UFBA 1636, UFBA 1645, on valves of Pinctada imbricata. Description. Colony encrusting (Fig. 3E), unilaminar. Autozooids hexagonal to rhomboidal (Fig. 3F), surrounded by 18–25 large, marginal pores. Frontal wall centrally imperforate, finely granular. Primary orifice transversely elliptical, wider than long, occupying about one-sixth of orifice length. Areolar pore transversely narrow, placed immediately proximal to orificial rim, visible in some zooids (Fig. 3F, arrow). Secondary orifice raised, surrounded by a calcification with small nodules around the rim. Suboral avicularium median, triangular, rostrum directed distally, extending about half to one-third of zooidal length. Spiramen (Fig. 3F, circle) crescentic, placed approximately in the center of the frontal wall, below the suboral avicularium. Gonozooid not observed. Remarks. Reptadeonella brasiliensis is among the commonest intertidal cheilostomes in NE Brazil, frequently found attached to hard substrata such as other bryozoans, shells and rocks (Almeida et al. 2015b). Distribution. Western Atlantic: Brazil (Ceará to Bahia; Fernando de Noronha) (Almeida et al. 2015b).Published as part of Almeida, Ana C. S., Souza, Facelucia B. C., Farias, Jamile, Alves, Orane F. S. & Vieira, Leandro M., 2018, Bryozoa on disarticulated bivalve shells from Todos os Santos Bay, northeastern Brazil, with the description of two new species, pp. 401-428 in Zootaxa 4434 (3) on page 407, DOI: 10.11646/zootaxa.4434.3.1, http://zenodo.org/record/129201
Chnoodes machadoi Krüger, Castro-Guedes & Almeida, 2016, sp. nov.
No full textChnoodes machadoi sp. nov. (Figure 7) Material examined. BRAZIL: Mato Grosso: “Cáceres, MT./ 13.XI. 1984 /Buzzi, Mielke, Elias/Casagrande leg./ Proj. Polonoroeste”, “Dptº Zool./UF - Paraná”, “ DZUP 188269 ”, “ HOLOTYPE / Chnoodes machadoi Krüger, Castro-Guedes & Almeida, 2015 ” [red label]; “Cáceres, MT./ 11.XI. 1984 /Buzzi, Mielke, Elias/Casagrande leg./ Proj. Polonoroeste”, “Dptº Zool./UF - Paraná”, [DZUP 188250, 188272], “ PARATYPE / Chnoodes machadoi Krüger, Castro-Guedes & Almeida, 2015 ” [yellow label]; “Cáceres, MT./ 13.XI. 1984 /Buzzi, Mielke, Elias/ Casagrande leg./Proj. Polonoroeste”, “Dptº Zool./UF - Paraná”, [DZUP 188249, 188270], “ PARATYPE / Chnoodes machadoi Krüger, Castro-Guedes & Almeida, 2015 ” [yellow label]; “Cáceres, MT/ 19.XI. 1984 /Buzzi, Mielke, Elias/Casagrande leg./Proj. Polonoroeste”, “Dptº Zool./UF - Paraná”, [DZUP 188266, 188267], “ PARATYPE / Chnoodes machadoi Krüger, Castro-Guedes & Almeida, 2015 ” [yellow label]; “Cáceres, MT./ 10.XI. 1984 /Buzzi, Mielke, Elias/Casagrande leg./Proj. Polonoroeste”, “Dptº Zool./UF - Paraná”, [DZUP 188271], “ PARATYPE / Chnoodes machadoi Krüger, Castro-Guedes & Almeida, 2015 ” [yellow label]. Goiás: “Dianópolis/GO, Brasil / 16–22.I. 1962 /J. Bechyné col.”, [DZUP 188237] “ PARATYPE / Chnoodes machadoi Krüger, Castro-Guedes & Almeida, 2015 ” [yellow label]. Male. Length 2.84–2.88 mm, width 2.08–2.16 mm. Body oval, with sparse white pubescence. Pronotum black with yellowish border and two small lateral spots. Elytra black with yellowish border and two yellowish areas below callus and near apex (Figs 7 A–D). Head, antennae and mouthparts orange. Meso- and metasternum dark brown or black; legs yellowish; epipleuron yellowish; first ventrites black or brownish (Fig. 7 B). Genitalia with basal lobe symmetrical, stout, shorter than parameres, apex bluntly pointed (Fig. 7 E). Parameres short and narrow (Fig. 7 F). Sipho rounded at apex, siphonal capsule rounded and short (Fig. 7 G). Female. Length 3.04–3.16 mm, width 2.20–2.24 mm. Genitalia with genital plates triangular, elongated, styli with setae (Fig. 7 H). Spermatheca C-shaped, short, apex narrow (Fig. 7 I). Etymology. This species is named in honor of the dedicated entomologist Doctor Angelo Barbosa Monteiro Machado, an expert in the taxonomy of dragonflies (Odonata) and endangered species, on the occasion of his 80 th birthday. Geographical Distribution. Brazil (MT, GO). Remarks. Chnoodes machadoi sp. nov. (Fig. 7) is similar to C. discomaculata (Fig. 3) and C. tarsalis (Fig. 6) in the color pattern, but is distinguished by the yellowish border of elytra. The male and female genitalia are also distinct.Published as part of Krüger, Thaysa C., Castro-Guedes, Camila F. & Almeida, Lúcia M., 2016, Two new species of Chnoodes Chevrolat (Coleoptera: Coccinellidae) from Brazil, pp. 269-283 in Zootaxa 4078 (1) on pages 279-281, DOI: 10.11646/zootaxa.4078.1.24, http://zenodo.org/record/26066
Alpheus buckupi Almeida, Terossi, Araujo-Silva & Mantelatto 2013
No full textAlpheus buckupi Almeida, Terossi, Araújo-Silva & Mantelatto, 2013 (Figure 1B) Alpheus buckupi Almeida et al., 2013: 440, figs. 1–4. Material examined. Brazil, São Paulo: 1 ♀ (parental with larvae), CCDB 3494, Ubatuba, Praia Grande, coll. F. Mantelatto, 27.xi.2002; 1 ♀ ov, CCDB 1205, São Sebastião, Araçá, coll. F. Mantelatto, 17.vi.2004; 1 ♀ ov, CCDB 1907, São Sebastião, Araçá, coll. F. Mantelatto et al., 04.v.2007; 1 ♂, 1 ♀ ov, CCDB 4883, São Sebastião, Araçá, coll. F. Mantelatto & L. Pardo, 10.ix.2013; 1 ♀, CCDB 5505, São Sebastião, Araçá, coll. F. Mantelatto et al., 02.xii.2014; 1 ♂, CCDB 3823, Cananéia, IO/ USP, coll. F. Mantelatto et al., 29.viii.2011. Distribution. Western Atlantic—Guadeloupe, Venezuela (Orinoco Delta), Brazil (Pará, Ceará, Rio Grande do Norte, Pernambuco, Alagoas, Sergipe, Bahia, São Paulo). Eastern Atlantic—São Tomé and Príncipe (Almeida et al. 2013; 2014; Barros-Alves et al. 2015; Pachelle et al. 2016). Previous records. Ubatuba, São Sebastião Island, São Sebastião and Santos (Almeida et al. 2013). Remarks. GenBank accession number: CCDB 1205—16 S (KU312967).Published as part of Almeida, Alexandre O., Terossi, Mariana, Buranelli, Raquel C., Castilho, Antonio L., Costa, Rogério C., Zara, Fernando J. & Mantelatto, Fernando L., 2018, Checklist of decapods (Crustacea) from the coast of São Paulo State (Brazil) supported by integrative molecular and morphological data: II. Infraorder Caridea: family Alpheidae, pp. 331-358 in Zootaxa 4450 (3) on pages 335-336, DOI: 10.11646/zootaxa.4450.3.2, http://zenodo.org/record/145255
Rhynchozoon brasiliensis ALMEIDA, SOUZA, MENEGOLA & VIEIRA 2017
No full textRhynchozoon brasiliensis Almeida, Souza, Menegola & Vieira, 2017 (Fig. 8C–F; Table 10) Rhynchozoon SP. 2: ALMEIDA et al. 2015A: P. 5. Rhynchozoon brasiliensis ALMEIDA, SOUZA, MENEgOLA & VIEIRA, 2017: P. 312, fIgS 84–89 (CUM SYN.). Material examined. UFBA 1620, UFBA 1623, UFBA 1625, UFBA 1644, UFBA 1647, UFBA 1651, UFBA 1653, UFBA 1657, UFBA 1658, UFBA 1662, UFBA 3357–3387, on valves of Pinctada imbricata. UFBA 1633, on valves of Plicatula gibbosa. Description. Colony encrusting (Fig. 8C), uni- to multilaminar. Zooids polygonal, separated by slightly raised lateral walls. Frontal wall smooth, with small rounded nodules and 10–16 large marginal pores. Primary orifice (Fig. 8D) small relative to zooidal length, commonly obscured by secondary orifice; distal edge with 10–20 rounded denticles; proximal edge with a broadly V-shaped sinus; condyles small, triangular, located at proximal corners of orifice; no oral spines. Secondary orifice well developed, formed by tubercles that can be fused due to increasing calcification. Suboral avicularium (Fig. 8E) small, single, oblique and directed distolaterally; rostrum triangular, with hooked tip and complete crossbar; foramen oval. Frontal avicularia small, diamond-shaped, located near zooidal margins, variable in orientation. Ovicell prominent (Fig. 8F), becoming immersed with increasing calcification; ooecia subglobular and frontally flat; ectooecium non-calcified frontally, leaving a large, circular tabula of completely calcified entooecium. Remarks. Rhynchozoon brasiliensis was misassigned to Rhynchozoon rostratum (Busk, 1856) (Souza 1989; Machado & Souza 1994) and Rhynchozoon verruculatum (Smitt, 1873) (Almeida et al. 2015a), but recently Almeida et al. (2017a) elucidated the identity of this species from Bahia. This species is commonly found attached to sponges, frequently those with a rugose external surface (Almeida et al. 2017a). Distribution. Western Atlantic: Brazil (Bahia) (Almeida et al. 2017a).Published as part of Almeida, Ana C. S., Souza, Facelucia B. C., Farias, Jamile, Alves, Orane F. S. & Vieira, Leandro M., 2018, Bryozoa on disarticulated bivalve shells from Todos os Santos Bay, northeastern Brazil, with the description of two new species, pp. 401-428 in Zootaxa 4434 (3) on page 418, DOI: 10.11646/zootaxa.4434.3.1, http://zenodo.org/record/129201
Erratum to: Effect of moderate red wine intake on cardiac prognosis after recent acute myocardial infarction of subjects with Type 2 diabetes mellitus (Diabetic Medicine, (2006), 23, 9, (974-981), 10.1111/j.1464-5491.2006.01886.x)
No full textIn an article by Marfella et al, the author name C. Saron is incorrect and should be listed as C. Sardu. Therefore the correct author list is: R. Marfella, F. Cacciapuoti, M. Siniscalchi, F. C. Sasso, F. Marchese, F. Cinone, E. Musacchio, M. A. Marfella, L. Ruggiero, G. Chiorazzo, D. Liberti, G. Chiorazzo, G. F. Nicoletti, C. Sardu, F. D'Andrea, C. Ammendola, M. Verza and L. Coppola.In an article by Marfella et al, the author name C. Saron is incorrect and should be listed as C. Sardu. Therefore the correct author list is: R. Marfella, F. Cacciapuoti, M. Siniscalchi, F. C. Sasso, F. Marchese, F. Cinone, E. Musacchio, M. A. Marfella, L. Ruggiero, G. Chiorazzo, D. Liberti, G. Chiorazzo, G. F. Nicoletti, C. Sardu, F. D'Andrea, C. Ammendola, M. Verza and L. Coppola
Hybrid Metaheuristics: Preface to the proceedings of HM2006
No full textThe International Workshop on Hybrid Metaheuristics reached its third edition with HM 2006. The active and successful participation in the past editions was a clear indication that the research community on metaheuristics and related areas felt the need for a forum to discuss specific aspects of hybridization of metaheuristics. The selection of papers for HM 2006 consolidated some of the mainstream issues that have emerged from the past editions. Firstly, there are prominent examples of effective hybrid techniques whose design and implementation were motivated by challenging real-world applications. A second important issue is that the research community on metaheuristics has become increasingly interested in and open to techniques and methods known from artificial intelligence (AI) and operations research (OR). The awareness of the need for a sound experimental methodology is a third keypoint. This aspect has gained more relevance and currency, even though there are still no widely agreed standard methodologies. As research on hybrid metaheuristics is mostly based on experimental methods, similar standards to those found in the evaluation of experiments in natural sciences can be expected. Scientific testing, a fourth notable aspect, emerges as a fundamental methodology for understanding the behavior of algorithms. The goal of scientific testing is to abstract from actual implementations and study, empirically and through predictive models, the effect of algorithmic components. This research approach can be particularly useful in the case of conjectures on metaheuristic algorithm behavior that, while being widespread in the community, have not yet been the subject of validation. Finally, a tendency to reconsider hybrid metaheuristics from a higher and more general perspective is emerging. Providing classifications, systematic analyses and surveys on important branches underlines a certain maturity of the relatively young field.
For the future, we envision a scenario in which some challenges have to be faced: – It should become common practice that experimental analysis meets high quality standards. This empirical approach is absolutely necessary to produce objective and reproducible results and to anchor the successes of metaheuristics in real-world applications. – Hybrid metaheuristic techniques have to be openly compared not just among themselves but also with state-of-the-art methods, from whatever field they are. By following this approach, researchers would be able to design techniques that meet the goal of solving a real-world problem and to consider the other approaches as rich sources of design components and ideas. – Scientific testing and theoretical models of algorithms for studying their behavior are still confined to a limited area of research. We believe that, by being able to explain rigorously algorithm behavior by means of sound empirical investigation and formal models, researchers would give the field a firmer status and give support to the development of real-world applications. The achievement of these goals will take some time in view of the difficult theoretical and practical problems involved in these challenges. Nevertheless, research is very active and has already produced some remarkable results and studies in this direction
Pseudoryssomus triangulus Almeida & Santos, 2014, sp. nov.
No full textPseudoryssomus triangulus sp. nov. (Fig. 11) Description of holotype (female). Length 5.26, width 3.89 mm. Form elongate oval, widest at middle of elytra, somewhat flattened dorsoventrally (Fig. 11 C). General color yellowish red, middle of thorax and abdomen yellowish red. Outline of pronotum and elytron discontinuous. Pronotum yellowish red, with a basal black spot, translucent at apex; finely, densely punctured; pubescence of semidecumbent yellowish hairs (Fig. 11 D). Elytra yellowish red with a triangular black spot, almost extending to apex, not reaching the humeral callus (Fig. 11 A). Elytral punctures intermixed coarse and fine, dense, slightly larger than on pronotum; sparse in the discal area. Antenna, mouthparts, hypomera, epipleura, and legs brownish yellow. Metaventrite finely, sparsely punctured medially and anteriorly; coarsely, densely punctured laterally and posteriorly with punctures large, often confluent. Abdominal ventrites coarsely punctured, punctures separated by about a diameter or less, punctures becoming coarser laterally (Fig. 11 B). First abdominal ventrite with postcoxal line incomplete, extending beyond middle of first ventrite; precoxal area coarsely punctured on base of cavity (Fig. 11 E). Genitalia with genital plates triangular, elongate, styli with setae; spermatheca elongate, uniform (Fig. 11 F, G). Male. Unknown. Etymology. The name of this species refers to the shape of the spot on the elytra. Discussion. Pseudoryssomus triangulus sp. nov. is somewhat similar to P. crucifer sp. nov., but is clearly distinguished by the shape of the spot and male and female genitalia. Type material. “Cayenne” “Muséum Paris/ 1930 /Coll. Sicard” “♀” [white label]. “ HOLOTYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [red label]. 1 ex. [MNHN]; “ Guyane Française,/Commune de Roura,/Montagne des Chevaux, /RN 2 PK22, 11.IX. 2011,/vitre, SEAG col.” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. [MNHN]; “ Guyane Française,/ Commune de Roura,/Montagne des Chevaux, /RN 2 PK22, 25.IX. 2011, /vitre, SEAG col.” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. “ DZUP / 289061 ” [DZUP]; “ Guyane Française, /Commune de Roura,/Montagne des Chevaux, /RN 2 PK22, 23.X. 2011, /vitre, SEAG col.” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. “ DZUP / 288989 ” [DZUP]; “ Guyane Française, /Commune de Roura,/Montagne des Chevaux, /RN 2 PK22, 07.XI.2011, 20 m/vitre, SEAG col.” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. “ DZUP / 289235 ” [DZUP]; “ Guyane Française,/Commune de Roura,/Montagne des Chevaux,/RN 2 PK22, 20 m,/ 02.X. 2011, solaire/automatique, SEAG col.” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. “ DZUP / 289898 ” [DZUP]; “ Guyane Française,/Commune de Roura, /Montagne des Chevaux, /RN 2 PK22, 20 m,/ 15.X. 2011, solaire/automatique, SEAG col.” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. “ DZUP / 289902 ” [DZUP]; “ Guyane Française,/Commune de Roura,/Montagne des Chevaux, /RN 2 PK22, 20 m, / 30.X. 2011, vitre, SEAG col.” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. “ DZUP / 289074 ” [DZUP]; “see notes” “ BRITISH GUIANA:/ Essequibo, R./Moraballi Creek./ 10 -X- 1929 /Oxf. Univ. Expedn. /B.M. 1929 - 485 ” “ 427 ” “ Oryssomus /det. R. Gordon 91 ” “♀” [white label]. “ PARATYPE / Pseudoryssomus / triangulus /Almeida & Santos, 2014 ” [yellow label]. 1 ex. [BMNH]. Geographical distribution. Commune de Roura, Montagne des Chevaux, French Guiana; Essequibo, Guyana (Fig. 16).Published as part of Almeida, Lúcia M. & Santos, Paula B., 2014, Synopsis of Oryssomini Gordon (Coleoptera: Coccinellidae) from the Neotropical region with new species of Oryssomus Mulsant, Pseudoryssomus Gordon and Gordonoryssomus Almeida & Lima in Zootaxa 3846 (1), DOI: 10.11646/zootaxa.3846.1.2, http://zenodo.org/record/25086
Gordonoryssomus limeirai Almeida & Santos, 2014, sp. nov.
No full textGordonoryssomus limeirai sp. nov. (Fig. 13) Description of holotype (male). Length 3.71, width 2.78 mm. Form elongate oval, widest at middle of elytra, somewhat flattened dorsoventrally (Fig. 13 C). General color and middle of thorax and abdomen brownish yellow. Outline of pronotum and elytron discontinuous. Pronotum yellowish red, with a basal triangular black spot, translucent at apex; finely, densely punctured; pubescence of semierect yellowish white hairs (Fig. 13 D). Elytra yellowish red with a large black spot, extending from the base almost to the apex, reaching the middle of humeral callus. With a brownish yellow spot in sutural margin along almost 2 / 3 of the suture (Fig. 13 A). Elytral punctures intermixed coarse and fine, dense, slightly larger than on pronotum; sparse in the discal area. Antenna, mouthparts, hypomera, epipleura, and legs brownish yellow. Metaventrite finely, sparsely punctured medially and anteriorly; coarsely, densely punctured laterally and posteriorly with punctures large, often confluent (Fig. 13 B). Abdominal ventrites coarsely punctured, punctures separated by about a diameter or less, punctures becoming coarser laterally. First abdominal ventrite with postcoxal line almost touching the posterior margin of the first abdominal ventrite; precoxal area coarsely punctured on base of cavity (Fig. 13 E). Genitalia simple; basal lobe equal in length to the paramere, lateral margin thickened and abruptly widened in apical half, apex bluntly pointed; paramere straight in lateral view, nearly parallel-sided (Fig. 13 G, H); sipho flattened, sinuous at apex (Fig. 13 F). FIGURE 13. Gordonoryssomus limeirai sp. nov. (A–E) Habitus: (A) dorsal; (B) ventral; (C) lateral; (D) frontal view. (E) Abdomen; (F–H) male genitalia: (F) sipho; (G) Tegmen, ventral; (H) lateral view. (I–J) Female terminalia: (I) spermatheca; (J) coxites. Female. Similar to male in all aspects externally. Genitalia with genital plates triangular, not elongated, styli with setae; spermatheca elongate, not uniform, with narrow apex (Fig. 13 I, J). Etymology. This species is named in honor of the dedicated entomologist, Dr. Francisco Limeira de Oliveira. Discussion. The color pattern is similar to that of G. delicatus, but it differs in length and the size of the sutural spot. Female genitalia with genital plate not elongate, somewhat triangular as in G. deyrollii, G. delicatus and G. mirnae. G. limeirai differs from all other species of the genus by the postcoxal line which almost touches the posterior margin of the first abdominal ventrite and male genitalia with wider basal lobe. Type material. “ BRAZIL (PI), Caracol/Parque Nacional Serra das/Confusões, Andorinha, 515 m,/ 09º08’ 27.8 ”S / 43 º 33 ’ 42.1 ”W / CZMA ” “Suspensa dupla (20 metros)/ 20-30.IX. 2013, J.A. Rafael,/F. Limeira de Oliveira &/T.T.A. Silva cols./ CZMA ” “♂” [white label]. “ HOLOTYPE / Gordonoryssomus / limeirai /Almeida & Santos, 2014 ” [red label]. 1 ex. [CZMA]; “ BRAZIL (PI), Caracol/Parque Nacional Serra das/Confusões, Andorinha, 515 m,/ 09º08’ 27.8 ”S / 43 º 33 ’ 42.1 ”W / CZMA ” “Suspensa dupla (20 metros)/ 20-30.IX. 2013, J.A. Rafael, / F. Limeira de Oliveira & /T.T.A. Silva cols./ CZMA ” “♀” [White label].“ PARATYPE / Gordonoryssomus / limeirai / Almeida & Santos, 2014 ” [yellow label]. 1 ex. “ DZUP / 245996 ” [DZUP]. Geographical distribution. Brazil (PI) (Fig. 17).Published as part of Almeida, Lúcia M. & Santos, Paula B., 2014, Synopsis of Oryssomini Gordon (Coleoptera: Coccinellidae) from the Neotropical region with new species of Oryssomus Mulsant, Pseudoryssomus Gordon and Gordonoryssomus Almeida & Lima in Zootaxa 3846 (1), DOI: 10.11646/zootaxa.3846.1.2, http://zenodo.org/record/25086
FIGURE 1 in Synopsis of Oryssomini Gordon (Coleoptera: Coccinellidae) from the Neotropical region with new species of Oryssomus Mulsant, Pseudoryssomus Gordon and Gordonoryssomus Almeida & Lima
No full textFIGURE 1. Tarsus and tarsal claw. (A, D): Pseudoryssomus formosus. (B, E): Gordonoryssomus deyrollii. (C, F): Oryssomus subterminatus.Published as part of Almeida, Lúcia M. & Santos, Paula B., 2014, Zootaxa 3846 (1), DOI: 10.11646/zootaxa.3846.1.2, http://zenodo.org/record/25086
- …
